Crystallography Open Database

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1557041 CIFC40 H49 Br N2 OP 1 21/n 111.1088; 21.1979; 15.9518
90; 108.641; 90		3559.32Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557042 CIFC42 H44 N2 Ni O3P -110.35522; 11.18263; 16.4194
100.307; 95.6535; 99.0466		1831.63Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557043 CIFC46 H52 Au Cl N2P 1 21/c 112.2795; 16.812; 19.2885
90; 93.6946; 90		3973.7Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557044 CIFC39 H44 N2I 41/a :238.4682; 38.4682; 9.5772
90; 90; 90		14172.4Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557667 CIFC21 H24 O2P 1 21/n 113.0157; 9.4167; 13.1769
90; 94.249; 90		1610.59Badmus, Fatimat O.; Malone, Joshua A.; Fronczek, Frank R.; Kartika, Rendy
Synthesis of functionalized tetrahydropyrans via cascade cycloaddition involving silyloxyallyl cation intermediates.
Chemical communications (Cambridge, England), 2020, 56, 5034-5037
1558026 CIFC31.75 H28 Ag F3 N2 O3.75 P SP 1 21/n 126.6378; 9.0287; 27.648
90; 110.854; 90		6213.9Rath, Bibhuti Bhusan; Kole, Goutam Kumar; Morris, Samuel Alexander; Vittal, Jagadese J.
Rotation of a helical coordination polymer by mechanical grinding.
Chemical communications (Cambridge, England), 2020, 56, 6289-6292
1558027 CIFC24 H20 N4P 1 21/c 110.4634; 8.3919; 10.5935
90; 98.999; 90		918.74Rath, Bibhuti Bhusan; Kole, Goutam Kumar; Morris, Samuel Alexander; Vittal, Jagadese J.
Rotation of a helical coordination polymer by mechanical grinding.
Chemical communications (Cambridge, England), 2020, 56, 6289-6292
1558135 CIFC18 H32 Cl Cu N7 O4C 1 c 19.682; 18.886; 24.789
90; 99.902; 90		4465Martínez-Camarena, Álvaro; Sánchez-Murcia, Pedro A; Blasco, Salvador; González, Leticia; García-España, Enrique
Unveiling the reaction mechanism of novel copper N-alkylated tetra-azacyclophanes with outstanding superoxide dismutase activity.
Chemical communications (Cambridge, England), 2020, 56, 7511-7514
1558152 CIFC31 H34 O4P -17.8821; 12.0559; 14.7116
86.518; 74.563; 78.674		1321.25Xu, Zhengshuai; Tang, Yitian; Shen, Chaoren; Zhang, Hongru; Gan, Yuxin; Ji, Xiaolei; Tian, Xinxin; Dong, Kaiwu
Nickel-catalyzed regio- and diastereoselective hydroarylative and hydroalkenylative cyclization of 1,6-dienes.
Chemical communications (Cambridge, England), 2020, 56, 7741-7744
1559148 CIFC24 H10 Cu2 N4 O10R -3 m :H18.3055; 18.3055; 52.0549
90; 90; 120		15106.2Wen, Hui-Min; Shao, Kai; Zhou, Wei; Li, Bin; Chen, Banglin
A novel expanded metal-organic framework for balancing volumetric and gravimetric methane storage working capacities.
Chemical communications (Cambridge, England), 2020, 56, 13117-13120
7124022 CIFC21.5 H20.5 N3 O2.5 ZnC 1 2/c 120.4932; 25.8736; 9.652
90; 99.109; 90		5053.3Ma, Xue; Zhang, Yanhao; Gao, Yu; Li, Xinglin; Wang, Cuijie; Yuan, Hang; Yu, Ajuan; Zhang, Shusheng; Cui, Yuanyuan
Revelation of the chiral recognition of alanine and leucine in an l-phenylalanine-based metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 1034-1037
7124466 CIFC16 H42 Cl2 Cu N4 O14P 32 2 18.729; 8.729; 33.58
90; 90; 120		2216Nakakoji, Takashi; Sato, Hirofumi; Ono, Daisuke; Miyake, Hiroyuki; Shinoda, Satoshi; Tsukube, Hiroshi; Kawasaki, Hideya; Arakawa, Ryuichi; Shizuma, Motohiro
Mass spectrometric detection of enantioselectivity in three-component complexation, copper(ii)-chiral tetradentate ligand-free amino acid in solution.
Chemical communications (Cambridge, England), 2019, 56, 54-57
7124515 CIFC41 H46 Cu F6 N6 PP -111.36657; 11.383; 17.2143
76.7608; 71.473; 64.7231		1898.3Karimata, Ayumu; Patil, Pradnya H.; Khaskin, Eugene; Lapointe, Sébastien; Fayzullin, Robert R.; Stampoulis, Pavlos; Khusnutdinova, Julia R.
Highly sensitive mechano-controlled luminescence in polymer films modified by dynamic Cu<sup>I</sup>-based cross-linkers.
Chemical communications (Cambridge, England), 2020, 56, 50-53
7124516 CIFC41 H46 Cu F6 N6 PC 1 c 110.8787; 19.7204; 18.0429
90; 94.732; 90		3857.59Karimata, Ayumu; Patil, Pradnya H.; Khaskin, Eugene; Lapointe, Sébastien; Fayzullin, Robert R.; Stampoulis, Pavlos; Khusnutdinova, Julia R.
Highly sensitive mechano-controlled luminescence in polymer films modified by dynamic Cu<sup>I</sup>-based cross-linkers.
Chemical communications (Cambridge, England), 2020, 56, 50-53
7124517 CIFC37 H38 Cu F6 N6 PP 1 21/c 115.83319; 17.71151; 12.63601
90; 97.3523; 90		3514.38Karimata, Ayumu; Patil, Pradnya H.; Khaskin, Eugene; Lapointe, Sébastien; Fayzullin, Robert R.; Stampoulis, Pavlos; Khusnutdinova, Julia R.
Highly sensitive mechano-controlled luminescence in polymer films modified by dynamic Cu<sup>I</sup>-based cross-linkers.
Chemical communications (Cambridge, England), 2020, 56, 50-53
7124518 CIFC43 H50 Cu F6 N6 PP c a 2120.03506; 13.30252; 15.03486
90; 90; 90		4007.04Karimata, Ayumu; Patil, Pradnya H.; Khaskin, Eugene; Lapointe, Sébastien; Fayzullin, Robert R.; Stampoulis, Pavlos; Khusnutdinova, Julia R.
Highly sensitive mechano-controlled luminescence in polymer films modified by dynamic Cu<sup>I</sup>-based cross-linkers.
Chemical communications (Cambridge, England), 2020, 56, 50-53
7124538 CIFC20 H24 B N O3P 1 21/c 110.2696; 18.4321; 9.8213
90; 97.243; 90		1844.2Rodriguez, Jessica; Adet, Nicolas; Saffon-Merceron, Nathalie; Bourissou, Didier
Au(i)/Au(iii)-Catalyzed C-N coupling.
Chemical communications (Cambridge, England), 2019, 56, 94-97
7124539 CIFC37 H48 Au F6 Li2 N2 O8 P S3P -19.8911; 14.4529; 17.441
102.378; 104.982; 109.989		2133.9Rodriguez, Jessica; Adet, Nicolas; Saffon-Merceron, Nathalie; Bourissou, Didier
Au(i)/Au(iii)-Catalyzed C-N coupling.
Chemical communications (Cambridge, England), 2019, 56, 94-97
7124541 CIFC47 H63 N O15 S4P 1 21/c 118.5665; 21.0808; 13.5866
90; 103.88; 90		5162.5Landovský, Tomáš; Eigner, Václav; Babor, Martin; Tichotová, Markéta; Dvořáková, Hana; Lhoták, Pavel
Regioselective S<sub>N</sub>Ar reaction of the phenoxathiin-based thiacalixarene as a route to a novel macrocyclic skeleton.
Chemical communications (Cambridge, England), 2019, 56, 78-81
7124542 CIFC45 H58 O13.08 S4P b c n39.4032; 10.2963; 23.4609
90; 90; 90		9518.3Landovský, Tomáš; Eigner, Václav; Babor, Martin; Tichotová, Markéta; Dvořáková, Hana; Lhoták, Pavel
Regioselective S<sub>N</sub>Ar reaction of the phenoxathiin-based thiacalixarene as a route to a novel macrocyclic skeleton.
Chemical communications (Cambridge, England), 2019, 56, 78-81
7124543 CIFC17 H17 N O5 SF d d 220.25; 21.622; 15.041
90; 90; 90		6585.6Fan, Huaqiang; Wan, Yi; Pan, Peng; Cai, Wenbin; Liu, Shihui; Liu, Chuanxu; Zhang, Yongqiang
A cascade approach to 3D cyclic carbamates via an ionic decarboxylative functionalization of olefinic oxamic acids.
Chemical communications (Cambridge, England), 2019, 56, 86-89
7124544 CIFC13 H15 N O3P 1 21/c 16.3499; 20.1527; 9.1657
90; 96.921; 90		1164.37Fan, Huaqiang; Wan, Yi; Pan, Peng; Cai, Wenbin; Liu, Shihui; Liu, Chuanxu; Zhang, Yongqiang
A cascade approach to 3D cyclic carbamates via an ionic decarboxylative functionalization of olefinic oxamic acids.
Chemical communications (Cambridge, England), 2019, 56, 86-89
7125425 CIFC15 H11 N2 O7 TbP 1 21/c 111.0348; 9.2759; 14.386
90; 97.876; 90		1458.6Wang, Xia; Wang, Yaxing; Wang, Yanlong; Liu, Hanzhou; Zhang, Yugang; Liu, Wei; Wang, Xiangxiang; Wang, Shuao
Color-tunable X-ray scintillation based on a series of isotypic lanthanide-organic frameworks.
Chemical communications (Cambridge, England), 2019, 56, 233-236
7125426 CIFC15 H15 Cl2 N O2 Pt SP 21 21 218.867; 12.232; 15.032
90; 90; 90		1630.4Yuan, Caixia; Wang, Weirong; Wang, Jianwei; Li, Xinhua; Wu, Yan-Bo; Li, Shaodong; Lu, Liping; Zhu, Miaoli; Xing, Shu; Fu, Xueqi
Potent and selective PTP1B inhibition by a platinum(ii) complex: possible implications for a new antitumor strategy.
Chemical communications (Cambridge, England), 2019, 56, 102-105
7125427 CIFC38 H38 N2 O4 S2P 1 21/c 116.4849; 10.3567; 19.7384
90; 98.596; 90		3332.1Chen, Si-Kai; Yang, Ju-Song; Dai, Kun-Long; Zhang, Fu-Min; Zhang, Xiao-Ming; Tu, Yong-Qiang
Exploration of a KI-catalyzed oxidation system for direct construction of bispyrrolidino[2,3-b]indolines and the total synthesis of (+)-WIN 64821.
Chemical communications (Cambridge, England), 2020, 56, 121-124
7125428 CIFC13 H12 B F I N O4I 1 2/a 127.8895; 6.8639; 34.3921
90; 105.296; 90		6350.48Fan, Wen-Xin; Li, Ji-Lin; Lv, Wen-Xin; Yang, Ling; Li, Qingjiang; Wang, Honggen
Synthesis of fluorinated amphoteric organoborons via iodofluorination of alkynyl and alkenyl MIDA boronates.
Chemical communications (Cambridge, England), 2020, 56, 82-85
7125429 CIFC13 H14 B F I N O4P b c a12.6367; 14.4997; 15.6349
90; 90; 90		2864.76Fan, Wen-Xin; Li, Ji-Lin; Lv, Wen-Xin; Yang, Ling; Li, Qingjiang; Wang, Honggen
Synthesis of fluorinated amphoteric organoborons via iodofluorination of alkynyl and alkenyl MIDA boronates.
Chemical communications (Cambridge, England), 2020, 56, 82-85
7125430 CIFC14 H16 B F I N O4P 1 21/c 112.7883; 11.1705; 10.9261
90; 102.02; 90		1526.59Fan, Wen-Xin; Li, Ji-Lin; Lv, Wen-Xin; Yang, Ling; Li, Qingjiang; Wang, Honggen
Synthesis of fluorinated amphoteric organoborons via iodofluorination of alkynyl and alkenyl MIDA boronates.
Chemical communications (Cambridge, England), 2020, 56, 82-85
7125431 CIFC22 H27 N3 O2P 21 21 218.4379; 10.5541; 22.3081
90; 90; 90		1986.64Ye, Xueqian; Pan, Yongkai; Yang, Xiaoyu
Direct enantioselective Mannich reactions of α-azido cyclic ketones: asymmetric construction of chiral azides possessing an α-quaternary stereocenter.
Chemical communications (Cambridge, England), 2019, 56, 98-101
7125432 CIFC19 H28 N4 O4P 1 21 112.1314; 10.4464; 15.7145
90; 95.952; 90		1980.75Ye, Xueqian; Pan, Yongkai; Yang, Xiaoyu
Direct enantioselective Mannich reactions of α-azido cyclic ketones: asymmetric construction of chiral azides possessing an α-quaternary stereocenter.
Chemical communications (Cambridge, England), 2019, 56, 98-101
7125440 CIFC16 H18 OP -19.0268; 12.5394; 12.5931
72.488; 70.192; 87.16		1276.75Lu, Xiao-Yu; Yan, Lu-Yu; Li, Jin-Song; Li, Jia-Mei; Zhou, Hai-Pin; Jiang, Run-Chuang; Liu, Chuang-Chuang; Lu, Ran; Hu, Rong
Base-free Ni-catalyzed Suzuki-type cross-coupling reactions of epoxides with boronic acids.
Chemical communications (Cambridge, England), 2019, 56, 109-112
7125441 CIFC14 H16 O2P 1 21/c 18.8117; 5.8923; 11.6496
90; 101.722; 90		592.25Inaba, Yuya; Yoneda, Tomoki; Kitagawa, Yuichi; Miyata, Kiyoshi; Hasegawa, Yasuchika; Inokuma, Yasuhide
Splitting and reorientation of π-conjugation by an unprecedented photo-rearrangement reaction.
Chemical communications (Cambridge, England), 2020, 56, 348-351
7125442 CIFC28 H34 O4P 1 21/c 18.6894; 5.8144; 23.4264
90; 99.837; 90		1166.19Inaba, Yuya; Yoneda, Tomoki; Kitagawa, Yuichi; Miyata, Kiyoshi; Hasegawa, Yasuchika; Inokuma, Yasuhide
Splitting and reorientation of π-conjugation by an unprecedented photo-rearrangement reaction.
Chemical communications (Cambridge, England), 2020, 56, 348-351
7125443 CIFC28 H30 O4P 1 21/c 18.7961; 5.8385; 22.8947
90; 99.317; 90		1160.27Inaba, Yuya; Yoneda, Tomoki; Kitagawa, Yuichi; Miyata, Kiyoshi; Hasegawa, Yasuchika; Inokuma, Yasuhide
Splitting and reorientation of π-conjugation by an unprecedented photo-rearrangement reaction.
Chemical communications (Cambridge, England), 2020, 56, 348-351
7125444 CIFC28 H30 O4P 1 21/c 112.6447; 17.9325; 10.8014
90; 103.228; 90		2384.24Inaba, Yuya; Yoneda, Tomoki; Kitagawa, Yuichi; Miyata, Kiyoshi; Hasegawa, Yasuchika; Inokuma, Yasuhide
Splitting and reorientation of π-conjugation by an unprecedented photo-rearrangement reaction.
Chemical communications (Cambridge, England), 2020, 56, 348-351
7125445 CIFC36 H32 I14 N4P -110.3325; 12.4358; 21.5144
95.149; 99.946; 98.812		2671.52Savastano, Matteo; Bazzicalupi, Carla; Gellini, Cristina; Bianchi, Antonio
Infinite supramolecular pseudo-polyrotaxane with poly[3]catenane axle: assembling nanosized rings from mono- and diatomic I<sup>-</sup> and I<sub>2</sub> tectons.
Chemical communications (Cambridge, England), 2020, 56, 551-554
7125446 CIFC36 H32 I16 N4P -110.1476; 13.0508; 21.8164
94.315; 100.436; 97.64		2801.6Savastano, Matteo; Bazzicalupi, Carla; Gellini, Cristina; Bianchi, Antonio
Infinite supramolecular pseudo-polyrotaxane with poly[3]catenane axle: assembling nanosized rings from mono- and diatomic I<sup>-</sup> and I<sub>2</sub> tectons.
Chemical communications (Cambridge, England), 2020, 56, 551-554
7125447 CIFC78 H62 B2 Fe N6 O8C 1 2 131.9544; 16.4618; 17.8159
90; 104.814; 90		9060.1Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125448 CIFC78 H62 B2 Fe N6 O8C 1 2 132.761; 16.907; 18.032
90; 106.009; 90		9600Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125449 CIFC78 H62 B2 Fe N6 O8C 1 2 132.45; 16.983; 18.105
90; 106.85; 90		9549Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125450 CIFC78 H62 B2 Fe N6 O8C 1 2 132.027; 16.64; 17.903
90; 105.183; 90		9208Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125451 CIFC78 H62 B2 Fe N6 O8C 1 2 131.8352; 16.6477; 17.9355
90; 105.495; 90		9160Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125452 CIFC156 H124 B4 Fe2 N12 O16P 1 21 118.08; 16.715; 32.015
90; 106.028; 90		9299Sun, Xiao-Peng; Tang, Zheng; Yao, Zi-Shuo; Tao, Jun
A homochiral 3D framework of mechanically interlocked 1D loops with solvent-dependent spin-state switching behaviors.
Chemical communications (Cambridge, England), 2020, 56, 133-136
7125453 CIFCu3 Li O6 Ru2C 1 2/m 15.208536; 9.023652; 6.027403
90; 106.64; 90		271.424Huang, Bin; Liu, Ziyi; Han, Yifeng; Zhao, Shuang; Wu, Meixia; Frank, Corey E.; Greenblatt, Martha; Croft, Mark; Quackenbush, Nicholas F.; Liu, Sizhan; Tyson, Trevor A.; Zhang, Lei; Sun, Junliang; Shan, Pengfei; Dai, Jianhong; Yu, Xiaohui; Cheng, Jinguang; Li, Man-Rong
Nonmetallic metal toward a pressure-induced bad-metal state in two-dimensional Cu<sub>3</sub>LiRu<sub>2</sub>O<sub>6</sub>.
Chemical communications (Cambridge, England), 2019, 56, 265-268
7125454 CIFC57 H55 N5 P2P 1 21/c 115.7507; 17.1271; 18.3836
90; 104.119; 90		4809.42Groß, C; Sun, Y.; Jost, T.; Grimm, T.; Klein, M. P.; Niedner-Schatteburg, G; Becker, S.; Thiel, W. R.
Generation of a zinc and rhodium containing metallomacrocycle by rearrangement of a six-coordinate precursor complex.
Chemical communications (Cambridge, England), 2020, 56, 368-371
7125455 CIFC123 H124 B Cl6 F7 N10 O6 P4 Rh2 S ZnP -115.3537; 19.4633; 22.6951
90.78; 106.494; 109.253		6096Groß, C; Sun, Y.; Jost, T.; Grimm, T.; Klein, M. P.; Niedner-Schatteburg, G; Becker, S.; Thiel, W. R.
Generation of a zinc and rhodium containing metallomacrocycle by rearrangement of a six-coordinate precursor complex.
Chemical communications (Cambridge, England), 2020, 56, 368-371
7125459 CIFC15 H12 Br F N2 O3P 1 21/c 115.548; 24.427; 8.266
90; 91.708; 90		3138Zaheer, Mohd Khalid; Gupta, Ekta; Kant, Ruchir; Mohanan, Kishor
Metal-free α-arylation of α-fluoro-α-nitroacetamides employing diaryliodonium salts.
Chemical communications (Cambridge, England), 2019, 56, 153-156
7125615 CIFC35 H46 Cu F6 N2 SbP b c a18.355; 18.334; 42.496
90; 90; 90		14301Parvin, Nasrina; Hossain, Jabed; George, Anjana; Parameswaran, Pattiyil; Khan, Shabana
N-heterocyclic silylene stabilized monocordinated copper(i)-arene cationic complexes and their application in click chemistry.
Chemical communications (Cambridge, England), 2019, 56, 273-276
7125616 CIFC34 H44 Cu F6 N2 SbC 1 c 124.087; 9.1915; 19.165
90; 124.966; 90		3477.1Parvin, Nasrina; Hossain, Jabed; George, Anjana; Parameswaran, Pattiyil; Khan, Shabana
N-heterocyclic silylene stabilized monocordinated copper(i)-arene cationic complexes and their application in click chemistry.
Chemical communications (Cambridge, England), 2019, 56, 273-276
7125617 CIFC28 H49 Cu F6 N3 Sb Si3P 21 21 2111.762; 14.725; 21.3
90; 90; 90		3689Parvin, Nasrina; Hossain, Jabed; George, Anjana; Parameswaran, Pattiyil; Khan, Shabana
N-heterocyclic silylene stabilized monocordinated copper(i)-arene cationic complexes and their application in click chemistry.
Chemical communications (Cambridge, England), 2019, 56, 273-276
7125618 CIFC38 H50 Cu F6 N4 SbP n m a13.623; 14.768; 20.118
90; 90; 90		4047Parvin, Nasrina; Hossain, Jabed; George, Anjana; Parameswaran, Pattiyil; Khan, Shabana
N-heterocyclic silylene stabilized monocordinated copper(i)-arene cationic complexes and their application in click chemistry.
Chemical communications (Cambridge, England), 2019, 56, 273-276
7125619 CIFC29 H51 Cu F6 N3 Sb Si3P 1 n 19.226; 11.541; 18.052
90; 98.414; 90		1901Parvin, Nasrina; Hossain, Jabed; George, Anjana; Parameswaran, Pattiyil; Khan, Shabana
N-heterocyclic silylene stabilized monocordinated copper(i)-arene cationic complexes and their application in click chemistry.
Chemical communications (Cambridge, England), 2019, 56, 273-276
7125620 CIFC49 H79 Cl2 Cu F6 N5 Sb Si3P 1 21/n 121.51; 12.624; 21.59
90; 96.299; 90		5827Parvin, Nasrina; Hossain, Jabed; George, Anjana; Parameswaran, Pattiyil; Khan, Shabana
N-heterocyclic silylene stabilized monocordinated copper(i)-arene cationic complexes and their application in click chemistry.
Chemical communications (Cambridge, England), 2019, 56, 273-276
7125621 CIFC3 H2 K N5 O5P 1 21/c 110.2767; 7.5626; 9.6783
90; 102.057; 90		735.59Liu, Tianlin; Liao, Sicheng; Song, Siwei; Wang, Kangcai; Jin, Yunhe; Zhang, Qinghua
Combination of gem-dinitromethyl functionality and a 5-amino-1,3,4-oxadiazole framework for zwitterionic energetic materials.
Chemical communications (Cambridge, England), 2019, 56, 209-212
7125622 CIFC3 H6 N6 O5P 1 21/c 110.165; 7.8116; 9.9589
90; 102.907; 90		770.81Liu, Tianlin; Liao, Sicheng; Song, Siwei; Wang, Kangcai; Jin, Yunhe; Zhang, Qinghua
Combination of gem-dinitromethyl functionality and a 5-amino-1,3,4-oxadiazole framework for zwitterionic energetic materials.
Chemical communications (Cambridge, England), 2019, 56, 209-212
7125623 CIFC3 H3 N5 O5P c a 218.2688; 6.1121; 13.2779
90; 90; 90		671.06Liu, Tianlin; Liao, Sicheng; Song, Siwei; Wang, Kangcai; Jin, Yunhe; Zhang, Qinghua
Combination of gem-dinitromethyl functionality and a 5-amino-1,3,4-oxadiazole framework for zwitterionic energetic materials.
Chemical communications (Cambridge, England), 2019, 56, 209-212
7125624 CIFC3 H4 N6 O5P 1 21/c 118.33; 6.1101; 13.6007
90; 107.342; 90		1454Liu, Tianlin; Liao, Sicheng; Song, Siwei; Wang, Kangcai; Jin, Yunhe; Zhang, Qinghua
Combination of gem-dinitromethyl functionality and a 5-amino-1,3,4-oxadiazole framework for zwitterionic energetic materials.
Chemical communications (Cambridge, England), 2019, 56, 209-212
7125625 CIFC15 H15 Cl N O PP -19.2947; 11.819; 14.46
85.569; 82.125; 67.021		1448.16Itazaki, Masumi; Matsutani, Takanari; Nochida, Tomoya; Moriuchi, Toshiyuki; Nakazawa, Hiroshi
Convenient synthesis of phosphinecarboxamide and phosphinecarbothioamide by hydrophosphination of isocyanates and isothiocyanates.
Chemical communications (Cambridge, England), 2020, 56, 443-445
7125626 CIFC98 H126 Li2 O17.5 Sn7P -114.3301; 15.1075; 26.1181
82.634; 76.623; 70.379		5173.7Steller, Beate G.; Fischer, Roland C.; Flock, Michaela; Hill, Michael S.; Liptrot, David J.; McMullin, Claire L.; Rajabi, Nasir A.; Tiefling, Kathrin; Wilson, Andrew S. S.
Reductive dehydrocoupling of diphenyltin dihydride with LiAlH<sub>4</sub>: selective synthesis and structures of the first bicyclo[2.2.1]heptastannane-1,4-diide and bicyclo[2.2.2]octastannane-1,4-diide.
Chemical communications (Cambridge, England), 2020, 56, 336-339
7125627 CIFC112 H140 Li2 O18 Sn8P 1 21/c 129.253; 14.3128; 26.5807
90; 90.276; 90		11129Steller, Beate G.; Fischer, Roland C.; Flock, Michaela; Hill, Michael S.; Liptrot, David J.; McMullin, Claire L.; Rajabi, Nasir A.; Tiefling, Kathrin; Wilson, Andrew S. S.
Reductive dehydrocoupling of diphenyltin dihydride with LiAlH<sub>4</sub>: selective synthesis and structures of the first bicyclo[2.2.1]heptastannane-1,4-diide and bicyclo[2.2.2]octastannane-1,4-diide.
Chemical communications (Cambridge, England), 2020, 56, 336-339
7125628 CIFC30 H42 Al Li O6P 1 21/c 111.8667; 20.5281; 12.5639
90; 106.359; 90		2936.67Steller, Beate G.; Fischer, Roland C.; Flock, Michaela; Hill, Michael S.; Liptrot, David J.; McMullin, Claire L.; Rajabi, Nasir A.; Tiefling, Kathrin; Wilson, Andrew S. S.
Reductive dehydrocoupling of diphenyltin dihydride with LiAlH<sub>4</sub>: selective synthesis and structures of the first bicyclo[2.2.1]heptastannane-1,4-diide and bicyclo[2.2.2]octastannane-1,4-diide.
Chemical communications (Cambridge, England), 2020, 56, 336-339
7125629 CIFC22 H40 Al Li O8P b c a14.856; 14.196; 23.825
90; 90; 90		5025Steller, Beate G.; Fischer, Roland C.; Flock, Michaela; Hill, Michael S.; Liptrot, David J.; McMullin, Claire L.; Rajabi, Nasir A.; Tiefling, Kathrin; Wilson, Andrew S. S.
Reductive dehydrocoupling of diphenyltin dihydride with LiAlH<sub>4</sub>: selective synthesis and structures of the first bicyclo[2.2.1]heptastannane-1,4-diide and bicyclo[2.2.2]octastannane-1,4-diide.
Chemical communications (Cambridge, England), 2020, 56, 336-339
7125630 CIFC94 H90 Li O8 Sn8P -114.2707; 14.2569; 31.4766
70.797; 67.696; 60.735		5086.5Steller, Beate G.; Fischer, Roland C.; Flock, Michaela; Hill, Michael S.; Liptrot, David J.; McMullin, Claire L.; Rajabi, Nasir A.; Tiefling, Kathrin; Wilson, Andrew S. S.
Reductive dehydrocoupling of diphenyltin dihydride with LiAlH<sub>4</sub>: selective synthesis and structures of the first bicyclo[2.2.1]heptastannane-1,4-diide and bicyclo[2.2.2]octastannane-1,4-diide.
Chemical communications (Cambridge, England), 2020, 56, 336-339
7125634 CIFC81 H118 N2 O10P -112.0829; 14.8643; 21.7404
89.974; 89.321; 75.472		3779.5Ji, Jiecheng; Li, Yizhou; Xiao, Chao; Cheng, Guo; Luo, Kui; Gong, Qiyong; Zhou, Dayang; Chruma, Jason J.; Wu, Wanhua; Yang, Cheng
Supramolecular enantiomeric and structural differentiation of amino acid derivatives with achiral pillar[5]arene homologs.
Chemical communications (Cambridge, England), 2020, 56, 161-164
7125635 CIFC101 H158 N2 O10P -112.4095; 20.4957; 21.0073
112.176; 96.805; 98.937		4795.2Ji, Jiecheng; Li, Yizhou; Xiao, Chao; Cheng, Guo; Luo, Kui; Gong, Qiyong; Zhou, Dayang; Chruma, Jason J.; Wu, Wanhua; Yang, Cheng
Supramolecular enantiomeric and structural differentiation of amino acid derivatives with achiral pillar[5]arene homologs.
Chemical communications (Cambridge, England), 2020, 56, 161-164
7125636 CIFC91 H131.01 N2 O10P -112.1416; 18.0125; 21.0862
71.058; 84.427; 84.478		4331Ji, Jiecheng; Li, Yizhou; Xiao, Chao; Cheng, Guo; Luo, Kui; Gong, Qiyong; Zhou, Dayang; Chruma, Jason J.; Wu, Wanhua; Yang, Cheng
Supramolecular enantiomeric and structural differentiation of amino acid derivatives with achiral pillar[5]arene homologs.
Chemical communications (Cambridge, England), 2020, 56, 161-164
7125637 CIFC111 H174 N2 O10P -112.9813; 20.477; 22.1377
67.441; 75.269; 83.834		5255.4Ji, Jiecheng; Li, Yizhou; Xiao, Chao; Cheng, Guo; Luo, Kui; Gong, Qiyong; Zhou, Dayang; Chruma, Jason J.; Wu, Wanhua; Yang, Cheng
Supramolecular enantiomeric and structural differentiation of amino acid derivatives with achiral pillar[5]arene homologs.
Chemical communications (Cambridge, England), 2020, 56, 161-164
7125638 CIFC23 H17 N O2P -19.2441; 9.5954; 10.6672
73.867; 70.65; 78.883		852.3Ajarul, Sk; Kayet, Anirban; Pati, Tanmay K.; Maiti, Dilip K.
A competitive and highly selective 7-, 6- and 5-annulation with 1,3-migration through C-H and N-H - alkyne coupling.
Chemical communications (Cambridge, England), 2020, 56, 474-477
7125639 CIFC24 H19 N O3P -18.893; 10.21; 11.258
80.88; 85.5; 69.03		942.2Ajarul, Sk; Kayet, Anirban; Pati, Tanmay K.; Maiti, Dilip K.
A competitive and highly selective 7-, 6- and 5-annulation with 1,3-migration through C-H and N-H - alkyne coupling.
Chemical communications (Cambridge, England), 2020, 56, 474-477
7125640 CIFFe40 Mo96 Na32 O625.43 P68I 41/a c d :227.3577; 27.3577; 38.0332
90; 90; 90		28465.7Zhang, Shan; Lu, Ying; Sun, Xiu-Wei; Li, Zhuo; Dang, Tian-Yi; Zhang, Zhong; Tian, Hong-Rui; Liu, Shu-Xia
Purely inorganic frameworks based on polyoxometalate clusters with abundant phosphate groups: single-crystal to single-crystal structural transformation and remarkable proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 391-394
7125641 CIFFe40 Mo96 Na32 O632 P68I 41/a c d :227.3329; 27.3329; 37.8621
90; 90; 90		28286Zhang, Shan; Lu, Ying; Sun, Xiu-Wei; Li, Zhuo; Dang, Tian-Yi; Zhang, Zhong; Tian, Hong-Rui; Liu, Shu-Xia
Purely inorganic frameworks based on polyoxometalate clusters with abundant phosphate groups: single-crystal to single-crystal structural transformation and remarkable proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 391-394
7125642 CIFC47 H54 O P2 Pd Si2C 1 2/c 120.6034; 11.5855; 35.7054
90; 97.72; 90		8445.7Takahashi, Rina; Kubota, Koji; Ito, Hajime
Air- and moisture-stable Xantphos-ligated palladium dialkyl complex as a precatalyst for cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 407-410
7125643 CIFC60 H34 O8C 1 2/m 135.192; 32.9021; 3.782
90; 92.815; 90		4373.9Wang, Bin; Lv, Xiu-Liang; Lv, Jie; Ma, Li; Lin, Rui-Biao; Cui, Hui; Zhang, Jian; Zhang, Zhangjing; Xiang, Shengchang; Chen, Banglin
A novel mesoporous hydrogen-bonded organic framework with high porosity and stability.
Chemical communications (Cambridge, England), 2019, 56, 66-69
7125644 CIFC36 H48 N6 O5P 1 21/c 110.423; 20.3482; 17.1498
90; 106.795; 90		3482.1Cho, Jihee; Verwilst, Peter; Kang, Minjung; Pan, Jia-Lin; Sharma, Amit; Hong, Chang Seop; Kim, Jong Seung; Kim, Sanghee
Crown ether-appended calix[2]triazolium[2]arene as a macrocyclic receptor for the recognition of the H<sub>2</sub>PO<sub>4</sub><sup>-</sup> anion.
Chemical communications (Cambridge, England), 2020, 56, 1038-1041
7125645 CIFC38 H52 N6 O6P 1 21/n 110.4036; 19.888; 18.5228
90; 103.284; 90		3729.95Cho, Jihee; Verwilst, Peter; Kang, Minjung; Pan, Jia-Lin; Sharma, Amit; Hong, Chang Seop; Kim, Jong Seung; Kim, Sanghee
Crown ether-appended calix[2]triazolium[2]arene as a macrocyclic receptor for the recognition of the H<sub>2</sub>PO<sub>4</sub><sup>-</sup> anion.
Chemical communications (Cambridge, England), 2020, 56, 1038-1041
7125646 CIFC40 H54 N6 O8P 1 21/c 19.699; 19.243; 21.345
90; 94.14; 90		3973.4Cho, Jihee; Verwilst, Peter; Kang, Minjung; Pan, Jia-Lin; Sharma, Amit; Hong, Chang Seop; Kim, Jong Seung; Kim, Sanghee
Crown ether-appended calix[2]triazolium[2]arene as a macrocyclic receptor for the recognition of the H<sub>2</sub>PO<sub>4</sub><sup>-</sup> anion.
Chemical communications (Cambridge, England), 2020, 56, 1038-1041
7125647 CIFC42 H48 B1.5 F6 N6 O9P 1 21/n 112.961; 19.32; 20.237
90; 93.98; 90		5055.3Cho, Jihee; Verwilst, Peter; Kang, Minjung; Pan, Jia-Lin; Sharma, Amit; Hong, Chang Seop; Kim, Jong Seung; Kim, Sanghee
Crown ether-appended calix[2]triazolium[2]arene as a macrocyclic receptor for the recognition of the H<sub>2</sub>PO<sub>4</sub><sup>-</sup> anion.
Chemical communications (Cambridge, England), 2020, 56, 1038-1041
7125648 CIFC21 H29 Cl N2 O6P -110.3139; 11.338; 12.384
63.811; 72.144; 69.542		1197.4Lei, Jian; Gao, Huaxin; Huang, Miaoling; Liu, Xiao; Mao, Yangfan; Xie, Xiaolan
Copper-catalyzed stereoselective alkylhydrazination of alkynes.
Chemical communications (Cambridge, England), 2020, 56, 920-923
7125649 CIFC44 H31 N5P 1 21/c 114.7683; 9.6009; 12.4544
90; 114.209; 90		1610.6Bousfiha, Asmae; Dimé, Abdou K D; Mankou-Makaya, Amelle; Echaubard, Julie; Berthelot, Mathieu; Cattey, Hélène; Romieu, Anthony; Roger, Julien; Devillers, Charles H.
Regioselective C-H amination of free base porphyrins via electrogenerated pyridinium-porphyrins and stabilization of easily oxidized amino-porphyrins by protonation.
Chemical communications (Cambridge, England), 2020, 56, 884-887
7125650 CIFC43 H55.26 B Cl4 F4 N5 O1.63 ZnP 1 21/n 111.0207; 15.2513; 27.7168
90; 99.255; 90		4598Bousfiha, Asmae; Dimé, Abdou K D; Mankou-Makaya, Amelle; Echaubard, Julie; Berthelot, Mathieu; Cattey, Hélène; Romieu, Anthony; Roger, Julien; Devillers, Charles H.
Regioselective C-H amination of free base porphyrins via electrogenerated pyridinium-porphyrins and stabilization of easily oxidized amino-porphyrins by protonation.
Chemical communications (Cambridge, England), 2020, 56, 884-887
7125651 CIFI O7 P Pb2P 1 21/n 17.374; 6.8144; 13.6077
90; 104.973; 90		660.56Zhang, Xiao-Han; Yang, Bing-Ping; Chen, Jin; Hu, Chun-Li; Fang, Zhi; Wang, Zujian; Mao, Jiang-Gao
A new iodate-phosphate Pb<sub>2</sub>(IO<sub>3</sub>)(PO<sub>4</sub>) achieving great improvement in birefringence activated by (IO<sub>3</sub>)<sup>-</sup> groups.
Chemical communications (Cambridge, England), 2020, 56, 635-638
7125652 CIFC192 H312 O21 P12 Ru6 S3P -123.3486; 24.9671; 25.2132
63.089; 83.896; 71.942		12450.7Fink, Daniel; Orth, Nicole; Linseis, Michael; Ivanović-Burmazović, Ivana; Winter, Rainer F.
Ring size matters: supramolecular isomerism in self-assembled redox-active tetra- and hexaruthenium macrocycles.
Chemical communications (Cambridge, England), 2020, 56, 1062-1065
7125653 CIFC134 H214 O14 P8 Ru4 S2P -111.9389; 17.383; 18.623
102.732; 98.198; 101.465		3623.7Fink, Daniel; Orth, Nicole; Linseis, Michael; Ivanović-Burmazović, Ivana; Winter, Rainer F.
Ring size matters: supramolecular isomerism in self-assembled redox-active tetra- and hexaruthenium macrocycles.
Chemical communications (Cambridge, England), 2020, 56, 1062-1065
7125654 CIFC92 H128 F6 N O12 PP 1 21/n 115.7124; 35.8329; 16.5563
90; 90.796; 90		9320.6Lu, Song-Bo; Chai, Hongxin; Ward, Jas S.; Quan, Mao; Zhang, Jin; Rissanen, Kari; Luo, Ray; Yang, Liu-Pan; Jiang, Wei
A 2,3-dialkoxynaphthalene-based naphthocage.
Chemical communications (Cambridge, England), 2020, 56, 888-891
7125655 CIFC207 H58 Cl6 F80 N20 O16 Re4P 1 21/c 119.63; 15.653; 32.561
90; 91.963; 90		9999Yadav, Pinky; Fridman, Natalia; Mizrahi, Amir; Gross, Zeev
Rhenium(i) sapphyrins: remarkable difference between the C<sub>6</sub>F<sub>5</sub> and CF<sub>3</sub>-substituted derivatives.
Chemical communications (Cambridge, England), 2020, 56, 980-983
7125656 CIFC31 H12 F12 N5 O3 ReP 1 21/n 111.9191; 13.1221; 19.0424
90; 101.594; 90		2917.5Yadav, Pinky; Fridman, Natalia; Mizrahi, Amir; Gross, Zeev
Rhenium(i) sapphyrins: remarkable difference between the C<sub>6</sub>F<sub>5</sub> and CF<sub>3</sub>-substituted derivatives.
Chemical communications (Cambridge, England), 2020, 56, 980-983
7125657 CIFK10 Mo18 O94 P2 Ti2P -112.375; 13.5901; 16.7251
103.174; 110.846; 94.834		2516.86Xu, Ming; Wang, Ting; Li, Fengyan; Xu, Wenjuan; Zheng, Yue; Xu, Lin
Water-soluble titanium-polyoxomolybdate with external μ<sub>3</sub> bridging oxygen coordination on a lacunary Keggin structure.
Chemical communications (Cambridge, England), 2020, 56, 1097-1100
7125658 CIFC4 H14 Na Ni O19 Ru2P c c n18.251; 9.2828; 10.1645
90; 90; 90		1722.1Li, Jing-Yu; Tian, Yu-Chen; Feng, Li-Na; Zhou, Zi-Qin; Wang, Lin-Lin; Yang, Jian-Hui; Liu, Bin
Enhancing magnetic hardness by sonication assisted synthesis of heterometallic carbonato spin-glass Na[Ni(H<sub>2</sub>O)<sub>4</sub>Ru<sub>2</sub>(CO<sub>3</sub>)<sub>4</sub>]·3H<sub>2</sub>O.
Chemical communications (Cambridge, England), 2020, 56, 1369-1372
7125659 CIFC24 H14 F N O2I 41/a :222.6155; 22.6155; 13.8933
90; 90; 90		7105.9Yang, Wan-Wan; Chen, Lu-Lu; Chen, Pei; Ye, Ya-Fang; Wang, Yan-Bo; Zhang, Xiao
Solvent-controlled divergent annulation of ynones and (iso)quinoline N-oxides: of 3-((iso)quinolin-1-yl)-4H-chromen-4-ones and 13H-isoquinolino[2,1-a]quinolin-13-ones.
Chemical communications (Cambridge, England), 2020, 56, 1183-1186
7125660 CIFC25 H15 Cl3 F N O2P -18.1531; 11.9242; 12.194
103.108; 101.744; 104.188		1076.41Yang, Wan-Wan; Chen, Lu-Lu; Chen, Pei; Ye, Ya-Fang; Wang, Yan-Bo; Zhang, Xiao
Solvent-controlled divergent annulation of ynones and (iso)quinoline N-oxides: of 3-((iso)quinolin-1-yl)-4H-chromen-4-ones and 13H-isoquinolino[2,1-a]quinolin-13-ones.
Chemical communications (Cambridge, England), 2020, 56, 1183-1186
7125661 CIFC25 H18 Br N O2P -17.411; 12.752; 21.926
77.759; 88.648; 85.507		2018.7Yang, Wan-Wan; Chen, Lu-Lu; Chen, Pei; Ye, Ya-Fang; Wang, Yan-Bo; Zhang, Xiao
Solvent-controlled divergent annulation of ynones and (iso)quinoline N-oxides: of 3-((iso)quinolin-1-yl)-4H-chromen-4-ones and 13H-isoquinolino[2,1-a]quinolin-13-ones.
Chemical communications (Cambridge, England), 2020, 56, 1183-1186
7125662 CIFC17 H20 O4P 1 21/c 18.2804; 8.1597; 23.4123
90; 90.403; 90		1581.83Yi, Xiangyan; Feng, Jiajun; Huang, Fei; Baell, Jonathan Bayldon
Metal-free C-C, C-O, C-S and C-N bond formation enabled by SBA-15 supported TFMSA.
Chemical communications (Cambridge, England), 2020, 56, 1243-1246
7125663 CIFC25 H22 O4P -110.7065; 12.0739; 17.4608
78.288; 83.301; 70.195		2076.61Yi, Xiangyan; Feng, Jiajun; Huang, Fei; Baell, Jonathan Bayldon
Metal-free C-C, C-O, C-S and C-N bond formation enabled by SBA-15 supported TFMSA.
Chemical communications (Cambridge, England), 2020, 56, 1243-1246
7125664 CIFC50 H76 K2 N6 O14 Te3C 1 2/c 124.4967; 14.9469; 32.9263
90; 95.346; 90		12003.5Puskarevsky, Nikolay A.; Smolentsev, Anton I.; Dmitriev, Alexey A.; Vargas-Baca, Ignacio; Gritsan, Nina P.; Beckmann, Jens; Zibarev, Andrey V.
Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by TeN chalcogen bonding.
Chemical communications (Cambridge, England), 2020, 56, 1113-1116
7125665 CIFC33 H25 N3 O4 SP 1 21/n 19.24; 12.733; 22.312
90; 96.38; 90		2608.8Kahar, Nilesh; Jadhav, Pankaj; Reddy, R. V. Ramana; Dawande, Sudam
A rhodium(ii) catalysed domino synthesis of azepino fused diindoles from isatin tethered N-sulfonyl-1,2,3-triazoles and indoles.
Chemical communications (Cambridge, England), 2020, 56, 1207-1210
7125666 CIFC29 H23 N3 O4 SP -110.8543; 11.773; 11.9282
106.799; 100.94; 116.237		1216.1Kahar, Nilesh; Jadhav, Pankaj; Reddy, R. V. Ramana; Dawande, Sudam
A rhodium(ii) catalysed domino synthesis of azepino fused diindoles from isatin tethered N-sulfonyl-1,2,3-triazoles and indoles.
Chemical communications (Cambridge, England), 2020, 56, 1207-1210
7125667 CIFC96 H86 N2 O4P -112.8892; 14.4794; 21.3927
100.456; 103.983; 94.972		3774.03Phukon, Jyotshna; Gogoi, Sanjib
Palladium(ii)-catalyzed vinylic geminal double C-H activation and alkyne annulation reaction: synthesis of pentafulvenes.
Chemical communications (Cambridge, England), 2020, 56, 1133-1136
7125668 CIFC85.01 H62.56 Cl0.94 N6 O24.27 S0.27P 1 21/m 113.0085; 24.5621; 16.7777
90; 92.839; 90		5354.2Wang, Weikun; Finnegan, Tyler J.; Lei, Zhiquan; Zhu, Xingrong; Moore, Curtis E.; Shi, Kejia; Badjić, Jovica D
Tuning the allosteric sequestration of anticancer drugs for developing cooperative nano-antidotes.
Chemical communications (Cambridge, England), 2020, 56, 1271-1274
7125669 CIFC18 H42 Na4 O22 S8C 1 2/c 135.431; 5.4941; 20.15
90; 108.517; 90		3719Gerken, James B.; Stamoulis, Alexios; Suh, Sung-Eun; Fischer, Nicholas D.; Kim, Yeon Jung; Guzei, Ilia A.; Stahl, Shannon S.
Efficient electrochemical synthesis of robust, densely functionalized water soluble quinones.
Chemical communications (Cambridge, England), 2020, 56, 1199-1202
7125670 CIFC14 H22 Na4 O17 S8C 1 2/c 119.151; 5.113; 29.21
90; 96.888; 90		2839.6Gerken, James B.; Stamoulis, Alexios; Suh, Sung-Eun; Fischer, Nicholas D.; Kim, Yeon Jung; Guzei, Ilia A.; Stahl, Shannon S.
Efficient electrochemical synthesis of robust, densely functionalized water soluble quinones.
Chemical communications (Cambridge, England), 2020, 56, 1199-1202
7125671 CIFC28 H23 Br I N O3 SP b c n14.8474; 30.043; 26.3798
90; 90; 90		11767Qiu, Yi-Feng; Niu, Yue-Jie; Song, Xian-Rong; Wei, Xi; Chen, Hui; Li, Shun-Xi; Wang, Xi-Cun; Huo, Congde; Quan, Zheng-Jun; Liang, Yong-Min
Iodine promoted cascade cycloisomerization of 1-en-6,11-diynes.
Chemical communications (Cambridge, England), 2020, 56, 1421-1424
7125672 CIFC29 H23 I N2 O3 SP n a 2125.67; 10.522; 9.8072
90; 90; 90		2648.9Qiu, Yi-Feng; Niu, Yue-Jie; Song, Xian-Rong; Wei, Xi; Chen, Hui; Li, Shun-Xi; Wang, Xi-Cun; Huo, Congde; Quan, Zheng-Jun; Liang, Yong-Min
Iodine promoted cascade cycloisomerization of 1-en-6,11-diynes.
Chemical communications (Cambridge, England), 2020, 56, 1421-1424
7125673 CIFC23 H15 N3P 1 21/n 19.549; 21.299; 9.583
90; 111.2; 90		1817.1Biswas, Aniruddha; Bera, Satabdi; Poddar, Puja; Dhara, Dibakar; Samanta, Rajarshi
Rh(iii)-Catalyzed tandem indole C4-arylamination/annulation with anthranils: access to indoloquinolines and their application in photophysical studies.
Chemical communications (Cambridge, England), 2020, 56, 1440-1443
7125674 CIFC56 H41 B F20 N O PP b a 235.439; 35.468; 7.9392
90; 90; 90		9979.2Livshits-Kritsman, Yulia; Tumanskii, Boris; Ménard, Gabriel; Dobrovetsky, Roman
Isolable cyclic (alkyl)(amino)carbene-phosphonyl radical adducts.
Chemical communications (Cambridge, England), 2020, 56, 1341-1344
7125675 CIFC26 H45 N O3 PP -19.5438; 9.7293; 15.436
90.316; 93.438; 110.986		1335.26Livshits-Kritsman, Yulia; Tumanskii, Boris; Ménard, Gabriel; Dobrovetsky, Roman
Isolable cyclic (alkyl)(amino)carbene-phosphonyl radical adducts.
Chemical communications (Cambridge, England), 2020, 56, 1341-1344
7125676 CIFC32 H41 N O PP 1 21/n 110.5072; 14.0611; 18.7738
90; 103.585; 90		2696.09Livshits-Kritsman, Yulia; Tumanskii, Boris; Ménard, Gabriel; Dobrovetsky, Roman
Isolable cyclic (alkyl)(amino)carbene-phosphonyl radical adducts.
Chemical communications (Cambridge, England), 2020, 56, 1341-1344
7125677 CIFC52 H82 N2 O6 P2P 1 21/c 118.3588; 15.6255; 17.7751
90; 95.085; 90		5079Livshits-Kritsman, Yulia; Tumanskii, Boris; Ménard, Gabriel; Dobrovetsky, Roman
Isolable cyclic (alkyl)(amino)carbene-phosphonyl radical adducts.
Chemical communications (Cambridge, England), 2020, 56, 1341-1344
7125678 CIFC21 H20 O7I 41/a :212.1107; 12.1107; 52.4973
90; 90; 90		7699.7Peng, Haiyun; Wan, Yinbo; Zhang, Yu; Deng, Guisheng
Synthesis of 2-alkenylfurans via a Ag(i)-catalyzed tandem cyclization/cross-coupling reaction of enynones with iodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 1417-1420
7125679 CIFC38 H46 Mg N3 O3.5 SiP 19.7605; 10.6398; 17.7151
94.6517; 98.1677; 90.4055		1814.73Vasilenko, Vladislav; Blasius, Clemens K.; Wadepohl, Hubert; Gade, Lutz H.
Borohydride intermediates pave the way for magnesium-catalysed enantioselective ketone reduction.
Chemical communications (Cambridge, England), 2020, 56, 1203-1206
7125680 CIFC38 H44 B Mg N3 O5P 21 21 2110.60635; 16.6805; 19.3703
90; 90; 90		3426.98Vasilenko, Vladislav; Blasius, Clemens K.; Wadepohl, Hubert; Gade, Lutz H.
Borohydride intermediates pave the way for magnesium-catalysed enantioselective ketone reduction.
Chemical communications (Cambridge, England), 2020, 56, 1203-1206
7125681 CIFC44 H46 F Mg N3 O5P 19.5675; 9.7347; 11.497
65.663; 88.065; 84.019		970.28Vasilenko, Vladislav; Blasius, Clemens K.; Wadepohl, Hubert; Gade, Lutz H.
Borohydride intermediates pave the way for magnesium-catalysed enantioselective ketone reduction.
Chemical communications (Cambridge, England), 2020, 56, 1203-1206
7125682 CIFC27 H24 O2P 1 21/n 19.9833; 11.7354; 34.8372
90; 97.4542; 90		4046.96Shoji, Taku; Sugiyama, Shuhei; Kobayashi, Yoshiaki; Yamazaki, Akari; Ariga, Yukino; Katoh, Ryuzi; Wakui, Hiroki; Yasunami, Masafumi; Ito, Shunji
Direct synthesis of 2-arylazulenes by [8+2] cycloaddition of 2H-cyclohepta[b]furan-2-ones with silyl enol ethers.
Chemical communications (Cambridge, England), 2020, 56, 1485-1488
7125683 CIFC13 H9 N SP 1 21/n 110.6375; 16.3123; 12.1927
90; 102.832; 90		2062.86Shoji, Taku; Sugiyama, Shuhei; Kobayashi, Yoshiaki; Yamazaki, Akari; Ariga, Yukino; Katoh, Ryuzi; Wakui, Hiroki; Yasunami, Masafumi; Ito, Shunji
Direct synthesis of 2-arylazulenes by [8+2] cycloaddition of 2H-cyclohepta[b]furan-2-ones with silyl enol ethers.
Chemical communications (Cambridge, England), 2020, 56, 1485-1488
7125684 CIFC15 H13 NP 1 21/c 18.9324; 5.7383; 21.1175
90; 98.605; 90		1070.23Shoji, Taku; Sugiyama, Shuhei; Kobayashi, Yoshiaki; Yamazaki, Akari; Ariga, Yukino; Katoh, Ryuzi; Wakui, Hiroki; Yasunami, Masafumi; Ito, Shunji
Direct synthesis of 2-arylazulenes by [8+2] cycloaddition of 2H-cyclohepta[b]furan-2-ones with silyl enol ethers.
Chemical communications (Cambridge, England), 2020, 56, 1485-1488
7125685 CIFC22 H22 O2C 1 c 112.8804; 9.8767; 13.8827
90; 101.424; 90		1731.11Shoji, Taku; Sugiyama, Shuhei; Kobayashi, Yoshiaki; Yamazaki, Akari; Ariga, Yukino; Katoh, Ryuzi; Wakui, Hiroki; Yasunami, Masafumi; Ito, Shunji
Direct synthesis of 2-arylazulenes by [8+2] cycloaddition of 2H-cyclohepta[b]furan-2-ones with silyl enol ethers.
Chemical communications (Cambridge, England), 2020, 56, 1485-1488
7125686 CIFC152 H254 As16 N16 Na6 O72 Sn14C 1 2/c 128.003; 38.235; 26.324
90; 99.404; 90		27806Zhu, Yu; Zhang, Jian; Zhang, Lei
A core-shell type alkyl-Sn-oxo cluster of {Sn<sub>14</sub>As<sub>16</sub>} bridged by 4-aminophenylarsonate ligands and incorporated with a {Na<sub>6</sub>} cluster.
Chemical communications (Cambridge, England), 2020, 56, 1433-1435
7125687 CIFC6 H5 N O2 SeP n a 218.3732; 13.5112; 5.8925
90; 90; 90		666.63He, Shichao; Allemond, Laynee L.; Dunning, Samuel G.; Reynolds, Joseph E.; Lynch, Vincent M.; Humphrey, Simon M.
In situ formation and solid-state oxidation of a triselenane NSeN-pincer MOF.
Chemical communications (Cambridge, England), 2020, 56, 1286-1289
7125688 CIFC12 H6 N2 Ni O5 Se3P 42/n c m :217.2294; 17.2294; 14.773
90; 90; 90		4385.4He, Shichao; Allemond, Laynee L.; Dunning, Samuel G.; Reynolds, Joseph E.; Lynch, Vincent M.; Humphrey, Simon M.
In situ formation and solid-state oxidation of a triselenane NSeN-pincer MOF.
Chemical communications (Cambridge, England), 2020, 56, 1286-1289
7125689 CIFC12 H16 N2 Ni O12 Se2P -16.7387; 7.6141; 9.7024
104.872; 91.645; 109.701		449.33He, Shichao; Allemond, Laynee L.; Dunning, Samuel G.; Reynolds, Joseph E.; Lynch, Vincent M.; Humphrey, Simon M.
In situ formation and solid-state oxidation of a triselenane NSeN-pincer MOF.
Chemical communications (Cambridge, England), 2020, 56, 1286-1289
7125690 CIFC28 H24 N3 O2 PP 1 21/c 19.7656; 22.5128; 11.5704
90; 110.736; 90		2378.98Mei, Ruhuai; Fang, Xinyue; He, Liang; Sun, Junmei; Zou, Liang; Ma, Wenbo; Ackermann, Lutz
Cobaltaelectro-catalyzed oxidative allene annulation by electro-removable hydrazides.
Chemical communications (Cambridge, England), 2020, 56, 1393-1396
7125691 CIFC16 H19 N OP -19.6378; 11.2515; 24.9151
87.202; 83.8; 78.211		2628.33Mei, Ruhuai; Fang, Xinyue; He, Liang; Sun, Junmei; Zou, Liang; Ma, Wenbo; Ackermann, Lutz
Cobaltaelectro-catalyzed oxidative allene annulation by electro-removable hydrazides.
Chemical communications (Cambridge, England), 2020, 56, 1393-1396
7125692 CIFC14 H24 N2 O5 S2P 1 21 17.25874; 6.61591; 18.72215
90; 91.4852; 90		898.795Escolano, Marcos; Guerola, Marta; Torres, Javier; Gaviña, Daniel; Alzuet-Piña, Gloria; Sánchez-Rosello, María; Del Pozo, Carlos
Organocatalytic enantioselective synthesis of 2,5,5-trisubstituted piperidines bearing a quaternary stereocenter. Vinyl sulfonamide as a new amine protecting group.
Chemical communications (Cambridge, England), 2020, 56, 1425-1428
7125693 CIFC89 H125 Cl3 N8 O12P 1 21/n 116.3019; 56.2981; 19.6862
90; 98.299; 90		17878.1Ye, Zecong; Wang, Jian; Kothapalli, Sudarshana Santhosh Kumar; Yang, Zhiyao; Chen, Lixi; Xu, Weitao; Cai, Yimin; Zhang, Tinghui; Xiao, Xin; Deng, Pengchi; Feng, Wen; Yuan, Lihua
Controlling the selective synthesis of [2]- and [3]rotaxanes by intermolecular steric hindrance between the macrocyclic hosts.
Chemical communications (Cambridge, England), 2020, 56, 1066-1069
7125694 CIFC137 H197 F12 N10 O20 P2P -114.0229; 16.6854; 17.42
100.477; 97.247; 114.357		3558Ye, Zecong; Wang, Jian; Kothapalli, Sudarshana Santhosh Kumar; Yang, Zhiyao; Chen, Lixi; Xu, Weitao; Cai, Yimin; Zhang, Tinghui; Xiao, Xin; Deng, Pengchi; Feng, Wen; Yuan, Lihua
Controlling the selective synthesis of [2]- and [3]rotaxanes by intermolecular steric hindrance between the macrocyclic hosts.
Chemical communications (Cambridge, England), 2020, 56, 1066-1069
7125695 CIFC74 H92 N6 S TiP 1 21/n 119.184; 16.616; 23.789
90; 110.8; 90		7089Gómez-Torres, Alejandra; Aguilar-Calderón, J Rolando; Saucedo, Carlos; Jordan, Aldo; Metta-Magaña, Alejandro; Pinter, Balazs; Fortier, Skye
Reversible oxidative-addition and reductive-elimination of thiophene from a titanium complex and its thermally-induced hydrodesulphurization chemistry.
Chemical communications (Cambridge, England), 2020, 56, 1545-1548
7125696 CIFC39 H58 Dy N5 O1.5 S4P 1 21/c 116.426; 14.4027; 20.5958
90; 111.107; 90		4545.6Canaj, Angelos B.; Dey, Sourav; Céspedes, Oscar; Wilson, Claire; Rajaraman, Gopalan; Murrie, Mark
There is nothing wrong with being soft: using sulfur ligands to increase axiality in a Dy(iii) single-ion magnet.
Chemical communications (Cambridge, England), 2020, 56, 1533-1536
7125697 CIFC36 H38 Cl6 Ga2 N6P -110.884; 16.71; 22.133
76.662; 86.906; 86.074		3904.6Robin, Perrine; Singh, Kuldip; Suntharalingam, Kogularamanan
Gallium(iii)-polypyridyl complexes as anti-osteosarcoma stem cell agents.
Chemical communications (Cambridge, England), 2020, 56, 1509-1512
7125698 CIFC15 H22 O3P 1 21 116.7954; 10.6132; 16.8783
90; 119.057; 90		2629.93Ruan, Qing-Feng; Jiang, Shi-Qin; Zheng, Xiao-Yun; Tang, Yu-Qian; Yang, Bao; Yi, Tao; Jin, Jing; Cui, Hui; Zhao, Zhongxiang
Pseudoguaianelactones A-C: three unusual sesquiterpenoids from Lindera glauca with anti-inflammatory activities by inhibiting the LPS-induced expression of iNOS and COX-2.
Chemical communications (Cambridge, England), 2020, 56, 1517-1520
7125699 CIFC15 H22 O3P 41 21 29.72709; 9.72709; 28.60837
90; 90; 90		2706.82Ruan, Qing-Feng; Jiang, Shi-Qin; Zheng, Xiao-Yun; Tang, Yu-Qian; Yang, Bao; Yi, Tao; Jin, Jing; Cui, Hui; Zhao, Zhongxiang
Pseudoguaianelactones A-C: three unusual sesquiterpenoids from Lindera glauca with anti-inflammatory activities by inhibiting the LPS-induced expression of iNOS and COX-2.
Chemical communications (Cambridge, England), 2020, 56, 1517-1520
7125700 CIFC32 H79 B3 Na O8 Si4 UP 1 21/n 117.3922; 14.5028; 20.3353
90; 108.868; 90		4853.67Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Uranium(iv) cyclobutadienyl sandwich compounds: synthesis, structure and chemical bonding.
Chemical communications (Cambridge, England), 2020, 56, 944-947
7125701 CIFC24 H64 B3 K O2 Si4 UP 1 21/c 115.5143; 15.8092; 16.0534
90; 97.572; 90		3903.1Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Uranium(iv) cyclobutadienyl sandwich compounds: synthesis, structure and chemical bonding.
Chemical communications (Cambridge, England), 2020, 56, 944-947
7125702 CIFC52 H123.7 B Na O4 Si8 UP 1 21/c 113.20381; 26.1179; 20.8685
90; 97.5838; 90		7133.67Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Uranium(iv) cyclobutadienyl sandwich compounds: synthesis, structure and chemical bonding.
Chemical communications (Cambridge, England), 2020, 56, 944-947
7125703 CIFC22 H22 N2 O4P 1 21/n 113.7113; 9.7397; 14.7226
90; 102.505; 90		1919.5Fu, Wei; Wang, Lianhui; Yang, Zi; Shen, Jiang-Shan; Tang, Fei; Zhang, Jiayi; Cui, Xiuling
Facile access to versatile aza-macrolides through iridium-catalysed cascade allyl-amination/macrolactonization.
Chemical communications (Cambridge, England), 2020, 56, 960-963
7125704 CIFC24 H20 F6 N2 O4P 1 21/c 110.163; 10.7505; 10.3964
90; 91.94; 90		1135.23Fu, Wei; Wang, Lianhui; Yang, Zi; Shen, Jiang-Shan; Tang, Fei; Zhang, Jiayi; Cui, Xiuling
Facile access to versatile aza-macrolides through iridium-catalysed cascade allyl-amination/macrolactonization.
Chemical communications (Cambridge, England), 2020, 56, 960-963
7125705 CIFC22 H20 F2 N2 O4P 1 21/c 116.6617; 9.8335; 12.61
90; 105.347; 90		1992.4Fu, Wei; Wang, Lianhui; Yang, Zi; Shen, Jiang-Shan; Tang, Fei; Zhang, Jiayi; Cui, Xiuling
Facile access to versatile aza-macrolides through iridium-catalysed cascade allyl-amination/macrolactonization.
Chemical communications (Cambridge, England), 2020, 56, 960-963
7125706 CIFC24 H26 N2 O6P b c a11.5668; 17.1785; 23.0513
90; 90; 90		4580.3Fu, Wei; Wang, Lianhui; Yang, Zi; Shen, Jiang-Shan; Tang, Fei; Zhang, Jiayi; Cui, Xiuling
Facile access to versatile aza-macrolides through iridium-catalysed cascade allyl-amination/macrolactonization.
Chemical communications (Cambridge, England), 2020, 56, 960-963
7125707 CIFC22 H22 N2 O4P 1 21/n 114.5996; 8.1161; 16.4481
90; 99.915; 90		1919.9Fu, Wei; Wang, Lianhui; Yang, Zi; Shen, Jiang-Shan; Tang, Fei; Zhang, Jiayi; Cui, Xiuling
Facile access to versatile aza-macrolides through iridium-catalysed cascade allyl-amination/macrolactonization.
Chemical communications (Cambridge, England), 2020, 56, 960-963
7125708 CIFC55 H82 N6 O2 UP -113.3531; 13.9911; 16.8717
103.238; 108.535; 108.528		2635.8Maria, Leonor; Bandeira, Nuno A. G.; Marçalo, Joaquim; Santos, Isabel C.; Gibson, John K.
CO<sub>2</sub> conversion to phenyl isocyanates by uranium(vi) bis(imido) complexes.
Chemical communications (Cambridge, England), 2020, 56, 431-434
7125709 CIFC48 H75 N5 O3 UP 1 21/n 115.5464; 13.2994; 23.2853
90; 103.112; 90		4688.9Maria, Leonor; Bandeira, Nuno A. G.; Marçalo, Joaquim; Santos, Isabel C.; Gibson, John K.
CO<sub>2</sub> conversion to phenyl isocyanates by uranium(vi) bis(imido) complexes.
Chemical communications (Cambridge, England), 2020, 56, 431-434
7125710 CIFK6 Mo18 O88 P2 Ti2P -112.375; 13.5901; 16.7251
103.174; 110.846; 94.834		2516.86Xu, Ming; Wang, Ting; Li, Fengyan; Xu, Wenjuan; Zheng, Yue; Xu, Lin
Water-soluble titanium-polyoxomolybdate with external μ<sub>3</sub> bridging oxygen coordination on a lacunary Keggin structure.
Chemical communications (Cambridge, England), 2020, 56, 1097-1100
7125711 CIFC77 H93 N3 O6P 1 21/n 122.357; 10.054; 28.899
90; 91.602; 90		6493.3Blanke, Meik; Balszuweit, Jan; Saccone, Marco; Wölper, Christoph; Doblas Jiménez, David; Mezger, Markus; Voskuhl, Jens; Giese, Michael
Photo-switching and -cyclisation of hydrogen bonded liquid crystals based on resveratrol.
Chemical communications (Cambridge, England), 2020, 56, 1105-1108
7125712 CIFC56 H66 N2 O5P -19.8815; 13.0611; 19.081
80.647; 83.99; 79.057		2378.8Blanke, Meik; Balszuweit, Jan; Saccone, Marco; Wölper, Christoph; Doblas Jiménez, David; Mezger, Markus; Voskuhl, Jens; Giese, Michael
Photo-switching and -cyclisation of hydrogen bonded liquid crystals based on resveratrol.
Chemical communications (Cambridge, England), 2020, 56, 1105-1108
7125713 CIFC37 H38 O3 SP 21 21 219.43565; 16.9768; 19.2055
90; 90; 90		3076.47You, Yong; Li, Ting-Ting; Yuan, Shu-Pei; Xie, Ke-Xin; Wang, Zhen-Hua; Zhao, Jian-Qiang; Zhou, Ming-Qiang; Yuan, Wei-Cheng
Catalytic asymmetric [4+2] cycloaddition of 1-((2-aryl)vinyl)naphthalen-2-ols with in situ generated ortho-quinone methides for the synthesis of polysubstituted chromanes.
Chemical communications (Cambridge, England), 2020, 56, 439-442
7125714 CIFC41 H42 Cl N O3P 1 21 111.8441; 10.6009; 15.1947
90; 103.393; 90		1855.9You, Yong; Li, Ting-Ting; Yuan, Shu-Pei; Xie, Ke-Xin; Wang, Zhen-Hua; Zhao, Jian-Qiang; Zhou, Ming-Qiang; Yuan, Wei-Cheng
Catalytic asymmetric [4+2] cycloaddition of 1-((2-aryl)vinyl)naphthalen-2-ols with in situ generated ortho-quinone methides for the synthesis of polysubstituted chromanes.
Chemical communications (Cambridge, England), 2020, 56, 439-442
7125715 CIFC22 H28 N2 O2P 1 21/c 118.3781; 9.6218; 11.0075
90; 101.862; 90		1904.9Viveki, Amol B.; Garad, Dnyaneshwar N.; Gonnade, Rajesh G.; Mhaske, Santosh B.
para-Selective copper-catalyzed C(sp<sup>2</sup>)-H amidation/dimerization of anilides via a radical pathway.
Chemical communications (Cambridge, England), 2020, 56, 1565-1568
7125716 CIFC26 H20 N2 O2P 1 21/c 112.6898; 8.3673; 19.2488
90; 106.184; 90		1962.8Viveki, Amol B.; Garad, Dnyaneshwar N.; Gonnade, Rajesh G.; Mhaske, Santosh B.
para-Selective copper-catalyzed C(sp<sup>2</sup>)-H amidation/dimerization of anilides via a radical pathway.
Chemical communications (Cambridge, England), 2020, 56, 1565-1568
7125717 CIFC43 H40 B F2 N3 O SC 1 2/c 132.32; 16.5482; 16.796
90; 118.803; 90		7871.8Hou, Yuqi; Liu, Qingyun; Zhao, Jianzhang
An exceptionally long-lived triplet state of red light-absorbing compact phenothiazine-styrylBodipy electron donor/acceptor dyads: a better alternative to the heavy atom-effect?
Chemical communications (Cambridge, England), 2020, 56, 1721-1724
7125718 CIFC45 H42 B F2 N3 O2 SP -18.3719; 11.6265; 21.171
91.635; 97.842; 102.352		1990.6Hou, Yuqi; Liu, Qingyun; Zhao, Jianzhang
An exceptionally long-lived triplet state of red light-absorbing compact phenothiazine-styrylBodipy electron donor/acceptor dyads: a better alternative to the heavy atom-effect?
Chemical communications (Cambridge, England), 2020, 56, 1721-1724
7125719 CIFC18 H38 Ag4 I6 N4P b c a14.9129; 14.9759; 15.1499
90; 90; 90		3383.5Zhang, Jin; Yao, Wan-Wan; Sang, Lei; Pan, Xue-Wei; Wang, Xiao-Zu; Liu, Wen-Long; Wang, Lifeng; Ren, Xiao-Ming
Multi-step structural phase transitions with novel symmetry breaking and inverse symmetry breaking characteristics in a [Ag<sub>4</sub>I<sub>6</sub>]<sup>2-</sup> cluster hybrid crystal.
Chemical communications (Cambridge, England), 2020, 56, 462-465
7125720 CIFC18 H38 Ag4 I6 N4P 1 21/c 115.0205; 15.0458; 15.0407
90; 90.269; 90		3399.1Zhang, Jin; Yao, Wan-Wan; Sang, Lei; Pan, Xue-Wei; Wang, Xiao-Zu; Liu, Wen-Long; Wang, Lifeng; Ren, Xiao-Ming
Multi-step structural phase transitions with novel symmetry breaking and inverse symmetry breaking characteristics in a [Ag<sub>4</sub>I<sub>6</sub>]<sup>2-</sup> cluster hybrid crystal.
Chemical communications (Cambridge, England), 2020, 56, 462-465
7125721 CIFC18 H38 Ag4 I6 N4P a -315.141; 15.141; 15.141
90; 90; 90		3471.1Zhang, Jin; Yao, Wan-Wan; Sang, Lei; Pan, Xue-Wei; Wang, Xiao-Zu; Liu, Wen-Long; Wang, Lifeng; Ren, Xiao-Ming
Multi-step structural phase transitions with novel symmetry breaking and inverse symmetry breaking characteristics in a [Ag<sub>4</sub>I<sub>6</sub>]<sup>2-</sup> cluster hybrid crystal.
Chemical communications (Cambridge, England), 2020, 56, 462-465
7125722 CIFC4 H2 Cl2 N4 O2P 1 21/c 116.0864; 12.7175; 7.1186
90; 99.45; 90		1436.55Chen, Sitong; Liu, Yuji; Feng, Yongan; Yang, Xianjin; Zhang, Qinghua
5,6-Fused bicyclic tetrazolo-pyridazine energetic materials.
Chemical communications (Cambridge, England), 2020, 56, 1493-1496
7125723 CIFC8 H10 N16 O5C 1 2/c 112.2036; 4.6757; 25.698
90; 93.484; 90		1463.6Chen, Sitong; Liu, Yuji; Feng, Yongan; Yang, Xianjin; Zhang, Qinghua
5,6-Fused bicyclic tetrazolo-pyridazine energetic materials.
Chemical communications (Cambridge, England), 2020, 56, 1493-1496
7125724 CIFC4 H4 N8 O5C 1 2/c 123.411; 5.0229; 15.2453
90; 101.545; 90		1756.4Chen, Sitong; Liu, Yuji; Feng, Yongan; Yang, Xianjin; Zhang, Qinghua
5,6-Fused bicyclic tetrazolo-pyridazine energetic materials.
Chemical communications (Cambridge, England), 2020, 56, 1493-1496
7125725 CIFC4 H2 N8 O4P 1 21/c 111.6487; 9.887; 14.4221
90; 106.486; 90		1592.72Chen, Sitong; Liu, Yuji; Feng, Yongan; Yang, Xianjin; Zhang, Qinghua
5,6-Fused bicyclic tetrazolo-pyridazine energetic materials.
Chemical communications (Cambridge, England), 2020, 56, 1493-1496
7125726 CIFC14 H14 Br F3 N2 O2P 1 21/n 19.2263; 15.7424; 11.8768
90; 108.325; 90		1637.56Du, Mengyuan; Yu, Longhui; Du, Ting; Li, Zhaokun; Luo, Yueyang; Meng, Xiangyu; Tian, Zhengtao; Zheng, Changwu; Cao, Weiguo; Zhao, Gang
N-Protecting group tuning of the enantioselectivity in Strecker reactions of trifluoromethyl ketimines to synthesize quaternary α-trifluoromethyl amino nitriles by ion pair catalysis.
Chemical communications (Cambridge, England), 2020, 56, 1581-1584
7125727 CIFC85 H68 F12 N6 O16 S4F d d d :220.677; 21.726; 36.877
90; 90; 90		16566Zhang, Wei; Wang, Linqin; Guo, Yu; Zhang, Biaobiao; Leandri, Valentina; Xu, Bo; Li, Zhuofeng; Gardner, James M.; Sun, Licheng; Kloo, Lars
Single crystal structure and opto-electronic properties of oxidized Spiro-OMeTAD.
Chemical communications (Cambridge, England), 2020, 56, 1589-1592
7125728 CIFC4 H12 Cd Cl N O6 S2P -18.0898; 8.7429; 9.3861
113.63; 100.423; 106.839		547.71Zhang, Guiyang; Yin, Jinlin; Song, Xueling; Fei, Honghan
A moisture-stable organosulfonate-based metal-organic framework with intrinsic self-trapped white-light emission.
Chemical communications (Cambridge, England), 2020, 56, 1325-1328
7125729 CIFC24 H20 N2 O4P 1 21/c 116.2065; 8.0264; 17.9481
90; 116.108; 90		2096.5Shi, Yuesen; Xing, Huimin; Huang, Tianle; Liu, Xuexin; Chen, Jian; Guo, Xiaoyu; Li, Guo-Bo; Wu, Yong
Divergent C-H activation synthesis of chalcones, quinolones and indoles.
Chemical communications (Cambridge, England), 2020, 56, 1585-1588
7125730 CIFC17 H21 Cl F N2 O RhP 1 21/n 18.543; 14.111; 14.684
90; 92.284; 90		1768.8Shi, Yuesen; Xing, Huimin; Huang, Tianle; Liu, Xuexin; Chen, Jian; Guo, Xiaoyu; Li, Guo-Bo; Wu, Yong
Divergent C-H activation synthesis of chalcones, quinolones and indoles.
Chemical communications (Cambridge, England), 2020, 56, 1585-1588
7125731 CIFC21 H20 I N O5P c a 2115.6909; 8.2225; 30.5829
90; 90; 90		3945.76Yu, Sifan; Chen, Jinzhou; Liu, Gengxin; Lei, Jinping; Hu, Wenhao; Qiu, Huang
A gold(i)-catalysed chemoselective three-component reaction between phenols, α-diazocarbonyl compounds and allenamides.
Chemical communications (Cambridge, England), 2020, 56, 1649-1652
7125732 CIFC22 H17 F12 N O8 S4P -110.7413; 11.0944; 13.5068
86.34; 69.593; 76.912		1469.2Martín-Mejías, Irene; Aragoncillo, Cristina; Yanai, Hikaru; Hoshikawa, Shoki; Fujimoto, Yuuki; Matsumoto, Takashi; Almendros, Pedro
A catalyst-free bis(triflyl)ethylation/benzannulation reaction: rapid access to carbazole-based superacidic carbon acids from alkynols.
Chemical communications (Cambridge, England), 2020, 56, 1795-1798
7125769 CIFC17 H11 Cl F3 N O4 SP 21 21 217.5867; 14.1693; 16.4025
90; 90; 90		1763.24Zhang, Zhen-Zhen; Zhang, Yongna; Duan, Hui-Xin; Deng, Zhuo-Fei; Wang, You-Qing
Enantioselective (3+2) cycloaddition via N-heterocyclic carbene-catalyzed addition of homoenolates to cyclic N-sulfonyl trifluoromethylated ketimines: synthesis of fused N-heterocycle γ-lactams.
Chemical communications (Cambridge, England), 2020, 56, 1553-1556
7125770 CIFC31 H22 F3 Fe N OP 21 21 2110.501; 12.436; 19.235
90; 90; 90		2511.9Jia, Lixiang; Liu, Xiaobing; Zhang, An-An; Wang, Tao; Hua, Yuanzhao; Li, Heng; Liu, Lantao
Synthesis of planar chiral ferrocenes via a Pd(0)-catalyzed syn-carbopalladation/asymmetric C-H alkenylation process.
Chemical communications (Cambridge, England), 2020, 56, 1737-1740
7125771 CIFC23 H18 Cl N O2 SP 1 21/n 112.324; 10.527; 15.383
90; 103.1; 90		1943.8Li, Qiuyun; Yuan, Xin; Li, Bin; Wang, Baiquan
The regioselective annulation of alkylidenecyclopropanes by Rh(iii)-catalyzed C-H/C-C activation to access spirocyclic benzosultams.
Chemical communications (Cambridge, England), 2020, 56, 1835-1838
7125772 CIFC27 H29 N O3 S2P -18.1485; 9.0966; 16.9811
103.951; 91.35; 100.482		1198.19Li, Qiuyun; Yuan, Xin; Li, Bin; Wang, Baiquan
The regioselective annulation of alkylidenecyclopropanes by Rh(iii)-catalyzed C-H/C-C activation to access spirocyclic benzosultams.
Chemical communications (Cambridge, England), 2020, 56, 1835-1838
7125773 CIFC15 H10 O2 SeP 1 21/c 114.7843; 6.4537; 13.8723
90; 108.104; 90		1258.08Song, Zengqiang; Ding, Chaochao; Wang, Shaoli; Dai, Qian; Sheng, Yaoguang; Zheng, Zhilong; Liang, Guang
Metal-free regioselective C-H chalcogenylation of coumarins/(hetero)arenes at ambient temperature.
Chemical communications (Cambridge, England), 2020, 56, 1847-1850
7125774 CIFC24 H19 Br N2 O3P -19.1003; 9.9785; 12.9831
74.611; 76.063; 64.264		1013.17Lei, Jie; Song, Gui-Ting; He, Liu-Jun; Luo, Ya-Fei; Tang, Dian-Yong; Lin, Hui-Kuan; Frett, Brendan; Li, Hong-Yu; Chen, Zhong-Zhu; Xu, Zhi-Gang
One-pot construction of functionalized aziridines and maleimides via a novel pseudo-Knoevenagel cascade reaction.
Chemical communications (Cambridge, England), 2020, 56, 2194-2197
7125775 CIFC25 H23 Br N2 O3P b c a10.532; 9.624; 43.85
90; 90; 90		4445Lei, Jie; Song, Gui-Ting; He, Liu-Jun; Luo, Ya-Fei; Tang, Dian-Yong; Lin, Hui-Kuan; Frett, Brendan; Li, Hong-Yu; Chen, Zhong-Zhu; Xu, Zhi-Gang
One-pot construction of functionalized aziridines and maleimides via a novel pseudo-Knoevenagel cascade reaction.
Chemical communications (Cambridge, England), 2020, 56, 2194-2197
7125776 CIFC24 H19 Br N2 O3P 21 21 2111.4032; 16.0552; 21.7377
90; 90; 90		3979.8Lei, Jie; Song, Gui-Ting; He, Liu-Jun; Luo, Ya-Fei; Tang, Dian-Yong; Lin, Hui-Kuan; Frett, Brendan; Li, Hong-Yu; Chen, Zhong-Zhu; Xu, Zhi-Gang
One-pot construction of functionalized aziridines and maleimides via a novel pseudo-Knoevenagel cascade reaction.
Chemical communications (Cambridge, England), 2020, 56, 2194-2197
7125777 CIFC30 H56 N6 P2 Se2P -19.2393; 13.1195; 16.0254
74.256; 75.947; 74.656		1772.13Naz, Nabila Rauf; Schnakenburg, Gregor; Mikeházi, Antal; Kelemen, Zsolt; Nyulászi, László; Boeré, René T; Streubel, Rainer
Janus bis(NHCs) tuned by heteroatom-bridge oxidation states.
Chemical communications (Cambridge, England), 2020, 56, 2646-2649
7125778 CIFC36 H78 Cl2 N6 O6 P2P -110.0162; 10.5594; 12.65
75.8224; 80.3081; 64.359		1166.45Naz, Nabila Rauf; Schnakenburg, Gregor; Mikeházi, Antal; Kelemen, Zsolt; Nyulászi, László; Boeré, René T; Streubel, Rainer
Janus bis(NHCs) tuned by heteroatom-bridge oxidation states.
Chemical communications (Cambridge, England), 2020, 56, 2646-2649
7125779 CIFC30 H57 Au2 Cl4 N6 O2 P2P -110.102; 10.857; 11.856
103.05; 97.19; 116.1		1099Naz, Nabila Rauf; Schnakenburg, Gregor; Mikeházi, Antal; Kelemen, Zsolt; Nyulászi, László; Boeré, René T; Streubel, Rainer
Janus bis(NHCs) tuned by heteroatom-bridge oxidation states.
Chemical communications (Cambridge, England), 2020, 56, 2646-2649
7125780 CIFC30 H56 N6 O2 P2P 1 21/c 18.688; 20.2501; 9.9593
90; 104.166; 90		1698.89Naz, Nabila Rauf; Schnakenburg, Gregor; Mikeházi, Antal; Kelemen, Zsolt; Nyulászi, László; Boeré, René T; Streubel, Rainer
Janus bis(NHCs) tuned by heteroatom-bridge oxidation states.
Chemical communications (Cambridge, England), 2020, 56, 2646-2649
7125781 CIFC25 H29 B Cl2 N7 O4 Re WP 1 21/c 18.0943; 21.8669; 17.322
90; 95.221; 90		3053.2Hill, Anthony F.; Watson, Lachlan J.
A heterobimetallic cumulenic μ-carbido complex.
Chemical communications (Cambridge, England), 2020, 56, 2356-2359
7125782 CIFC14 H10 O4 Re2 SeP -17.4306; 7.9327; 13.4641
103.629; 95.575; 104.678		735.66Hill, Anthony F.; Watson, Lachlan J.
A heterobimetallic cumulenic μ-carbido complex.
Chemical communications (Cambridge, England), 2020, 56, 2356-2359
7125783 CIFC34 H26 N2 O4 ZnP -19.2972; 10.943; 14.517
97.63; 104.8; 98.88		1387.7Li, Ni-Ya; Chen, Jing-Min; Tang, Xiao-Yan; Zhang, Guo-Ping; Liu, Dong
Reversible single-crystal-to-single-crystal conversion of a photoreactive coordination network for rewritable optical memory storage.
Chemical communications (Cambridge, England), 2020, 56, 1984-1987
7125784 CIFC34 H26 N2 O4 ZnP -19.3272; 11.065; 14.204
94.76; 106.97; 98.35		1375Li, Ni-Ya; Chen, Jing-Min; Tang, Xiao-Yan; Zhang, Guo-Ping; Liu, Dong
Reversible single-crystal-to-single-crystal conversion of a photoreactive coordination network for rewritable optical memory storage.
Chemical communications (Cambridge, England), 2020, 56, 1984-1987
7125785 CIFC34 H26 N2 O4 ZnP -19.1552; 10.954; 14.582
97.65; 104.66; 98.55		1376.6Li, Ni-Ya; Chen, Jing-Min; Tang, Xiao-Yan; Zhang, Guo-Ping; Liu, Dong
Reversible single-crystal-to-single-crystal conversion of a photoreactive coordination network for rewritable optical memory storage.
Chemical communications (Cambridge, England), 2020, 56, 1984-1987
7125786 CIFC48 H60 O10 Si2P 21 21 2110.316; 14.614; 31.37
90; 90; 90		4729.3Zhao, Yachen; Wang, Shengyang; Yu, Biao
Dimerization of aldosuloses and aldonolactones into branched higher carbon sugars.
Chemical communications (Cambridge, England), 2020, 56, 2020-2022
7125787 CIFC48 H59 O10 Si2P 1 21 110.622; 29.251; 15.2076
90; 91.972; 90		4722.3Zhao, Yachen; Wang, Shengyang; Yu, Biao
Dimerization of aldosuloses and aldonolactones into branched higher carbon sugars.
Chemical communications (Cambridge, England), 2020, 56, 2020-2022
7125788 CIFC27 H44 O12 SiP 18.5482; 9.8574; 10.674
82.65; 67.265; 68.386		771.1Zhao, Yachen; Wang, Shengyang; Yu, Biao
Dimerization of aldosuloses and aldonolactones into branched higher carbon sugars.
Chemical communications (Cambridge, England), 2020, 56, 2020-2022
7125789 CIFC18 H24 O10P 1 21 111.2418; 6.7238; 12.8125
90; 102.473; 90		945.61Zhao, Yachen; Wang, Shengyang; Yu, Biao
Dimerization of aldosuloses and aldonolactones into branched higher carbon sugars.
Chemical communications (Cambridge, England), 2020, 56, 2020-2022
7125790 CIFC17 H28 O8 SiP 1 21 19.696; 21.8766; 10.7943
90; 114.535; 90		2082.9Zhao, Yachen; Wang, Shengyang; Yu, Biao
Dimerization of aldosuloses and aldonolactones into branched higher carbon sugars.
Chemical communications (Cambridge, England), 2020, 56, 2020-2022
7125791 CIFC20 H16 N2 O4P 21 21 219.9589; 10.3374; 17.3428
90; 90; 90		1785.43Ruan, Sai; Zhong, Xia; Chen, Quangang; Feng, Xiaoming; Liu, Xiaohua
An asymmetric hydrocyanation/Michael reaction of α-diazoacetates via Cu(i)/chiral guanidine catalysis.
Chemical communications (Cambridge, England), 2020, 56, 2155-2158
7125792 CIFC54 H74 As2 Ge2 N4P 1 21/c 121.3357; 15.3136; 16.1347
90; 93.71; 90		5260.6Cui, Haiyan; Xiao, Dengmengfei; Zhang, Li; Ruan, Huapeng; Fang, Yong; Zhao, Yue; Tan, Gengwen; Zhao, Lili; Frenking, Gernot; Driess, Matthias; Wang, Xinping
Isolable cyclic radical cations of heavy main-group elements.
Chemical communications (Cambridge, England), 2020, 56, 2167-2170
7125793 CIFC70 H74 Al F36 Ge2 N4 O4 P2C 1 2/c 129.5048; 16.5238; 19.4551
90; 118.25; 90		8355.2Cui, Haiyan; Xiao, Dengmengfei; Zhang, Li; Ruan, Huapeng; Fang, Yong; Zhao, Yue; Tan, Gengwen; Zhao, Lili; Frenking, Gernot; Driess, Matthias; Wang, Xinping
Isolable cyclic radical cations of heavy main-group elements.
Chemical communications (Cambridge, England), 2020, 56, 2167-2170
7125794 CIFC76 H79 Al As2 F37 Ge2 N4 O4C m c 2119.7185; 19.794; 22.651
90; 90; 90		8840.9Cui, Haiyan; Xiao, Dengmengfei; Zhang, Li; Ruan, Huapeng; Fang, Yong; Zhao, Yue; Tan, Gengwen; Zhao, Lili; Frenking, Gernot; Driess, Matthias; Wang, Xinping
Isolable cyclic radical cations of heavy main-group elements.
Chemical communications (Cambridge, England), 2020, 56, 2167-2170
7125795 CIFC19 H21 B Br F2 N3 OP 21 21 217.6521; 11.7979; 20.7618
90; 90; 90		1874.35Ren, Xiaojie; Zhang, Fan; Luo, Hongchen; Liao, Lide; Song, Xiangzhi; Chen, Wenqiang
Red-emitting boron difluoride complexes with a mega-large Stokes shift and unexpectedly high fluorescence quantum yield.
Chemical communications (Cambridge, England), 2020, 56, 2159-2162
7125796 CIFC34 H25 Mn O3 P2P 1 21/c 117.9568; 9.8598; 20.8696
90; 90.927; 90		3694.5Kireev, Nikolay V.; Filippov, Oleg A.; Gulyaeva, Ekaterina S.; Shubina, Elena S.; Vendier, Laure; Canac, Yves; Sortais, Jean-Baptiste; Lugan, Noël; Valyaev, Dmitry A.
Bis[diphenylphosphino]methane and its bridge-substituted analogues as chemically non-innocent ligands for H<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 2139-2142
7125797 CIFC34 H27 Mn O3 P2P 1 21/n 112.7697; 16.2687; 13.7964
90; 97.868; 90		2839.2Kireev, Nikolay V.; Filippov, Oleg A.; Gulyaeva, Ekaterina S.; Shubina, Elena S.; Vendier, Laure; Canac, Yves; Sortais, Jean-Baptiste; Lugan, Noël; Valyaev, Dmitry A.
Bis[diphenylphosphino]methane and its bridge-substituted analogues as chemically non-innocent ligands for H<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 2139-2142
7125798 CIFC36 H24 Ag3 Cl3 F9 N O6 P2P 1 21/n 112.3904; 26.0236; 13.0998
90; 94.131; 90		4212.96Yang, Jin-Sen; Zhang, Miao-Miao; Han, Zhen; Li, Hai-Yang; Li, Lin-Ke; Dong, Xi-Yan; Zang, Shuang-Quan; Mak, Thomas C. W.
A new silver cluster that emits bright-blue phosphorescence.
Chemical communications (Cambridge, England), 2020, 56, 2451-2454
7125799 CIFC42 H64 Br2 P2P 1 21/c 115.4258; 10.0015; 26.8115
90; 93.829; 90		4127.3Ohtsuki, Kazuaki; Walsgrove, Henry T. G.; Hayashi, Yoshihiro; Kawauchi, Susumu; Patrick, Brian O.; Gates, Derek P.; Ito, Shigekazu
Diels-Alder reactions of 1-phosphabutadienes: a highly selective route to P[double bond, length as m-dash]C-substituted phosphacyclohexenes.
Chemical communications (Cambridge, England), 2020, 56, 774-777
7125800 CIFC46 H74 Cl6 P2 PdP 1 21/n 19.4889; 22.8642; 23.9461
90; 101.002; 90		5099.8Ohtsuki, Kazuaki; Walsgrove, Henry T. G.; Hayashi, Yoshihiro; Kawauchi, Susumu; Patrick, Brian O.; Gates, Derek P.; Ito, Shigekazu
Diels-Alder reactions of 1-phosphabutadienes: a highly selective route to P[double bond, length as m-dash]C-substituted phosphacyclohexenes.
Chemical communications (Cambridge, England), 2020, 56, 774-777
7125801 CIFC44 H70 P2P 1 21/n 120.2458; 10.192; 39.8543
90; 95.509; 90		8185.8Ohtsuki, Kazuaki; Walsgrove, Henry T. G.; Hayashi, Yoshihiro; Kawauchi, Susumu; Patrick, Brian O.; Gates, Derek P.; Ito, Shigekazu
Diels-Alder reactions of 1-phosphabutadienes: a highly selective route to P[double bond, length as m-dash]C-substituted phosphacyclohexenes.
Chemical communications (Cambridge, England), 2020, 56, 774-777
7125802 CIFC20 H20 N4 S4I b a m13.634; 23.059; 6.8383
90; 90; 90		2149.9Makarov, Alexander Yu; Volkova, Yulia M.; Shundrin, Leonid A.; Dmitriev, Alexey A.; Irtegova, Irina G.; Bagryanskaya, Irina Yu; Shundrina, Inna K.; Gritsan, Nina P.; Beckmann, Jens; Zibarev, Andrey V.
Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states.
Chemical communications (Cambridge, England), 2020, 56, 727-730
7125803 CIFC14 H20 Cl8 Ga2 N2 O S4P 1 21/c 112.8899; 21.9751; 10.8024
90; 98.673; 90		3024.86Makarov, Alexander Yu; Volkova, Yulia M.; Shundrin, Leonid A.; Dmitriev, Alexey A.; Irtegova, Irina G.; Bagryanskaya, Irina Yu; Shundrina, Inna K.; Gritsan, Nina P.; Beckmann, Jens; Zibarev, Andrey V.
Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states.
Chemical communications (Cambridge, England), 2020, 56, 727-730
7125804 CIFC13 H13 F3 N3 O3 S3P -17.7987; 11.1508; 11.7044
68.737; 82.028; 70.79		895.51Makarov, Alexander Yu; Volkova, Yulia M.; Shundrin, Leonid A.; Dmitriev, Alexey A.; Irtegova, Irina G.; Bagryanskaya, Irina Yu; Shundrina, Inna K.; Gritsan, Nina P.; Beckmann, Jens; Zibarev, Andrey V.
Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states.
Chemical communications (Cambridge, England), 2020, 56, 727-730
7125805 CIFC24 H26 Cl8 Ga2 N6 S4P b c a17.0008; 12.4285; 18.4315
90; 90; 90		3894.5Makarov, Alexander Yu; Volkova, Yulia M.; Shundrin, Leonid A.; Dmitriev, Alexey A.; Irtegova, Irina G.; Bagryanskaya, Irina Yu; Shundrina, Inna K.; Gritsan, Nina P.; Beckmann, Jens; Zibarev, Andrey V.
Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states.
Chemical communications (Cambridge, England), 2020, 56, 727-730
7125806 CIFC20 H18 Cl4 Ga N4 S4I 1 2/m 115.6419; 6.7683; 25.762
90; 100.258; 90		2683.8Makarov, Alexander Yu; Volkova, Yulia M.; Shundrin, Leonid A.; Dmitriev, Alexey A.; Irtegova, Irina G.; Bagryanskaya, Irina Yu; Shundrina, Inna K.; Gritsan, Nina P.; Beckmann, Jens; Zibarev, Andrey V.
Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states.
Chemical communications (Cambridge, England), 2020, 56, 727-730
7125807 CIFC20 H20 N4 S5C 1 2/m 126.008; 7.0295; 14.98
90; 120.32; 90		2364.1Makarov, Alexander Yu; Volkova, Yulia M.; Shundrin, Leonid A.; Dmitriev, Alexey A.; Irtegova, Irina G.; Bagryanskaya, Irina Yu; Shundrina, Inna K.; Gritsan, Nina P.; Beckmann, Jens; Zibarev, Andrey V.
Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states.
Chemical communications (Cambridge, England), 2020, 56, 727-730
7125808 CIFC12 H10 F6 N2 O6 S6P -17.9057; 11.8661; 13.7217
110.248; 104.718; 97.976		1131Makarov, Alexander Yu; Volkova, Yulia M.; Shundrin, Leonid A.; Dmitriev, Alexey A.; Irtegova, Irina G.; Bagryanskaya, Irina Yu; Shundrina, Inna K.; Gritsan, Nina P.; Beckmann, Jens; Zibarev, Andrey V.
Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states.
Chemical communications (Cambridge, England), 2020, 56, 727-730
7125809 CIFC32 H20 Cl8 Ga2 N4 S4P -17.196; 10.589; 15.296
100.19; 99.014; 98.771		1113.3Makarov, Alexander Yu; Volkova, Yulia M.; Shundrin, Leonid A.; Dmitriev, Alexey A.; Irtegova, Irina G.; Bagryanskaya, Irina Yu; Shundrina, Inna K.; Gritsan, Nina P.; Beckmann, Jens; Zibarev, Andrey V.
Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states.
Chemical communications (Cambridge, England), 2020, 56, 727-730
7125810 CIFC34 H56 B10 N4 O2 Si2P -114.0023; 18.12; 19.4694
97.894; 110.964; 98.644		4461.6Xiong, Yun; Yao, Shenglai; Szilvási, Tibor; Ruzicka, Ales; Driess, Matthias
Homocoupling of CO and isocyanide mediated by a C,C'-bis(silylenyl)-substituted ortho-carborane.
Chemical communications (Cambridge, England), 2020, 56, 747-750
7125811 CIFC50 H74 B10 N6 Si2P 1 21/n 116.3688; 16.3773; 20.0064
90; 96.451; 90		5329.29Xiong, Yun; Yao, Shenglai; Szilvási, Tibor; Ruzicka, Ales; Driess, Matthias
Homocoupling of CO and isocyanide mediated by a C,C'-bis(silylenyl)-substituted ortho-carborane.
Chemical communications (Cambridge, England), 2020, 56, 747-750
7125812 CIFC67 H18 F15 N6 O4 Rh2P 1 21/n 110.5064; 13.7489; 36.4349
90; 97.87; 90		5213.5Samala, Srinivas; Dutta, Ranjan; He, Qing; Park, Yeonju; Chandra, Brijesh; Lynch, Vincent M.; Jung, Young Mee; Sessler, Jonathan L.; Lee, Chang-Hee
A robust bis-rhodium(i) complex of π-extended planar, anti-aromatic hexaphyrin[1.0.1.0.1.0].
Chemical communications (Cambridge, England), 2020, 56, 758-761
7125813 CIFC23 H20 Cl N5 O2 SP 1 21/c 15.093; 18.689; 24.05
90; 93.684; 90		2284Zhao, Xiaolei; Zheng, Wei; Zhang, Yi; Huang, Wei
cis alkenes stabilized by intramolecular sulphurπ interactions.
Chemical communications (Cambridge, England), 2020, 56, 814-817
7125814 CIFC23 H20 Cl N5 O2 SP 1 21/n 110.9364; 10.8589; 38.833
90; 91.052; 90		4610.9Zhao, Xiaolei; Zheng, Wei; Zhang, Yi; Huang, Wei
cis alkenes stabilized by intramolecular sulphurπ interactions.
Chemical communications (Cambridge, England), 2020, 56, 814-817
7125815 CIFC23 H21 Cl N4 SP 1 21/c 114.7727; 7.6261; 19.442
90; 95.253; 90		2181.1Zhao, Xiaolei; Zheng, Wei; Zhang, Yi; Huang, Wei
cis alkenes stabilized by intramolecular sulphurπ interactions.
Chemical communications (Cambridge, England), 2020, 56, 814-817
7125816 CIFC24 H23 Cl N4 SP -17.9024; 9.4958; 15.018
78.986; 87.8; 85.372		1102.3Zhao, Xiaolei; Zheng, Wei; Zhang, Yi; Huang, Wei
cis alkenes stabilized by intramolecular sulphurπ interactions.
Chemical communications (Cambridge, England), 2020, 56, 814-817
7125817 CIFC23 H21 Cl N4 SP -112.225; 12.945; 15.227
114.539; 95.09; 93.604		2170.2Zhao, Xiaolei; Zheng, Wei; Zhang, Yi; Huang, Wei
cis alkenes stabilized by intramolecular sulphurπ interactions.
Chemical communications (Cambridge, England), 2020, 56, 814-817
7125818 CIFC31 H29 N13 OP 1 21/c 116.6866; 6.5849; 34.8753
90; 94.826; 90		3818.5Wang, Yijie; Liu, Di; Yin, Jianbo; Shang, Yanxue; Du, Juan; Kang, Zixi; Wang, Rongming; Chen, Yanli; Sun, Daofeng; Jiang, Jianzhuang
An ultrafast responsive NO<sub>2</sub> gas sensor based on a hydrogen-bonded organic framework material.
Chemical communications (Cambridge, England), 2020, 56, 703-706
7125819 CIFC34 H37 N14 O3P 1 21/c 116.2396; 6.5461; 33.4443
90; 90.79; 90		3555Wang, Yijie; Liu, Di; Yin, Jianbo; Shang, Yanxue; Du, Juan; Kang, Zixi; Wang, Rongming; Chen, Yanli; Sun, Daofeng; Jiang, Jianzhuang
An ultrafast responsive NO<sub>2</sub> gas sensor based on a hydrogen-bonded organic framework material.
Chemical communications (Cambridge, England), 2020, 56, 703-706
7125820 CIFCs12 K3 Mn O292 Si6 Ta18 W54P -121.631; 23.063; 31.541
80.614; 81.403; 70.344		14544Wu, Hai-Yang; Hu, Hai; Qin, Chao; Huang, Peng; Wang, Xin-Long; Su, Zhong-Min
Self-assembly and lithium storage performance of a nanoscale polyoxometalate based on the {MnTa<sub>18</sub>} cluster.
Chemical communications (Cambridge, England), 2020, 56, 2403-2406
7125821 CIFC108 H59 B2 Cl5 F40 Zr3P n a 2120.8992; 15.4821; 30.637
90; 90; 90		9913Budzelaar, Peter H. M.; Hughes, David L.; Bochmann, Manfred; Macchioni, Alceo; Rocchigiani, Luca
H<sub>2</sub> activation by zirconaziridinium ions: σ-bond metathesis versus frustrated Lewis pair reactivity.
Chemical communications (Cambridge, England), 2020, 56, 2542-2545
7125822 CIFC16 H13 Cl N2C 1 2/c 119.4385; 9.3554; 17.415
90; 123.697; 90		2634.9Liu, Jidan; Xu, Erjie; Jiang, Jinyuan; Huang, Zeng; Zheng, Liyao; Liu, Zhao-Qing
Copper-mediated tandem ring-opening/cyclization reactions of cyclopropanols with aryldiazonium salts: synthesis of N-arylpyrazoles.
Chemical communications (Cambridge, England), 2020, 56, 2202-2205
7125823 CIFC23 H17 N O3P 1 21/c 113.0762; 6.6583; 21.175
90; 106.715; 90		1765.7Xie, Ya-Sa; Huang, Run-Feng; Li, Ran; Zhang, Chuan-Bao; Fu, Ji-Ya; Zhao, Li-Li; Yuan, Jin-Fang
Metal-free [3+3] benzannulation of 1-indanylidene-malononitrile with Morita-Baylis-Hillman carbonates: direct access to functionalized fluorene and fluorenone derivatives.
Chemical communications (Cambridge, England), 2020, 56, 1948-1951
7125824 CIFC37 H26 N2 OP 1 n 17.9242; 9.1825; 18.631
90; 93; 90		1353.81Li, Xiaobin; Zhang, Chengxi; Wang, Chenchen; Ye, Wenqiang; Zhang, Qian; Zhang, Zhiyun; Su, Jianhua; Chen, Yifeng; Tian, He
Modular synthesis of (C-10 to C-13)-substituted-9,14-diaryl-9,14-dihydrodibenzo[a,c]phenazines via a subsequent Buchwald-Hartwig amination and C-H amination strategy.
Chemical communications (Cambridge, England), 2020, 56, 2260-2263
7125825 CIFC27 H22 N2 O2C 1 2/c 144.109; 10.1725; 9.6069
90; 90.827; 90		4310.2Yu, Qing; Zhang, Xiaodong; Wu, Shou-Ting; Chen, Huaiyu; Zhang, Qi-Long; Xu, Hong; Huang, Ya-Li; Zhu, Bi-Xue; Ni, Xin-Long
Twisted Schiff-base macrocycle showing excited-state intramolecular proton-transfer (ESIPT): assembly and sensing properties.
Chemical communications (Cambridge, England), 2020, 56, 2304-2307
7125826 CIFC24 H26 Br N O2P -18.8862; 9.2731; 14.1317
90.728; 101.126; 116.691		1014.27Zhao, Quan-Sheng; Xu, Guo-Qiang; Xu, Ji-Tao; Wang, Zhu-Yin; Xu, Peng-Fei
A lutidine-promoted photoredox catalytic atom-transfer radical cyclization reaction for the synthesis of 4-bromo-3,3-dialkyl-octahydro-indol-2-ones.
Chemical communications (Cambridge, England), 2020, 56, 2206-2209
7125827 CIFC24 H26 Cl N O2P -18.7322; 9.3453; 13.9189
90.64; 99.884; 116.102		1000.03Zhao, Quan-Sheng; Xu, Guo-Qiang; Xu, Ji-Tao; Wang, Zhu-Yin; Xu, Peng-Fei
A lutidine-promoted photoredox catalytic atom-transfer radical cyclization reaction for the synthesis of 4-bromo-3,3-dialkyl-octahydro-indol-2-ones.
Chemical communications (Cambridge, England), 2020, 56, 2206-2209
7125828 CIFC18 H16 F2 N2 O4P 21 21 219.0527; 10.5367; 17.9083
90; 90; 90		1708.19Kong, Wei-Xin; Xie, Shi-Jing; Cao, Chen-Yao-Zi; Zhang, Chao-Wei; Wang, Chuanyong; Duan, Wei-Liang
Asymmetric construction of quaternary α-nitro amides by palladium-catalyzed C(sp<sup>3</sup>)-H arylation.
Chemical communications (Cambridge, England), 2020, 56, 2292-2295
7125829 CIFC86 H142 Al2 K2 N6 O2 Si4P 1 2/n 113.00568; 19.41913; 19.00129
90; 105.701; 90		4619.87Anker, Mathew D.; Schwamm, Ryan J.; Coles, Martyn P.
Synthesis and reactivity of a terminal aluminium-imide bond.
Chemical communications (Cambridge, England), 2020, 56, 2288-2291
7125830 CIFC76 H114 Al2 K2 N6 O6 Si4P 1 21/n 110.22272; 26.48398; 15.22743
90; 93.9074; 90		4113.07Anker, Mathew D.; Schwamm, Ryan J.; Coles, Martyn P.
Synthesis and reactivity of a terminal aluminium-imide bond.
Chemical communications (Cambridge, England), 2020, 56, 2288-2291
7125831 CIFC22 H18 N2 O2C 1 2/c 124.857; 8.2443; 17.849
90; 104.733; 90		3537.5He, Shiyu; Yan, Xufei; Lei, Yanxi; Xiang, Haifeng; Zhou, Xiangge
Rhodium-catalyzed annulative coupling of N-aryl-2-aminopyridine and propargylic amine via selective C-C and C-H bond activation.
Chemical communications (Cambridge, England), 2020, 56, 2284-2287
7125832 CIFC20 H20 F3 N OP b c a6.3469; 21.271; 25.867
90; 90; 90		3492.2Liang, Xiaoyu; Guo, Pan; Yang, Wenjie; Li, Meng; Jiang, Chengzhou; Sun, Wangbin; Loh, Teck-Peng; Jiang, Yaojia
Stereoselective synthesis of trifluoromethyl-substituted 2H-furan-amines from enaminones.
Chemical communications (Cambridge, England), 2020, 56, 2043-2046
7125833 CIFC38 H98 Fe K N3 O8 Si6P 1 21/n 115.4864; 17.4686; 21.7327
90; 92.335; 90		5874.4Werncke, Christian Gunnar; Müller, Igor
The ambiguous behaviour of diphosphines towards the quasilinear iron(i) complex [Fe(N(SiMe<sub>3</sub>)<sub>2</sub>)<sub>2</sub>]<sup>-</sup> - between inertness, P-C bond cleavage and C-C double bond isomerisation.
Chemical communications (Cambridge, England), 2020, 56, 2268-2271
7125834 CIFC50 H82 Fe K N2 O6 P2 Si4P -111.66; 13.061; 20.875
73.368; 74.116; 75.985		2883.1Werncke, Christian Gunnar; Müller, Igor
The ambiguous behaviour of diphosphines towards the quasilinear iron(i) complex [Fe(N(SiMe<sub>3</sub>)<sub>2</sub>)<sub>2</sub>]<sup>-</sup> - between inertness, P-C bond cleavage and C-C double bond isomerisation.
Chemical communications (Cambridge, England), 2020, 56, 2268-2271
7125835 CIFC56 H82.48 Fe K N O8 P2 Si2P -113.1704; 15.3361; 15.4398
97.045; 103.248; 95.214		2989.7Werncke, Christian Gunnar; Müller, Igor
The ambiguous behaviour of diphosphines towards the quasilinear iron(i) complex [Fe(N(SiMe<sub>3</sub>)<sub>2</sub>)<sub>2</sub>]<sup>-</sup> - between inertness, P-C bond cleavage and C-C double bond isomerisation.
Chemical communications (Cambridge, England), 2020, 56, 2268-2271
7125836 CIFC58 H98 Fe K N2 O8 P2 Si4P 1 21/c 112.5633; 35.5283; 15.3551
90; 99.326; 90		6763.2Werncke, Christian Gunnar; Müller, Igor
The ambiguous behaviour of diphosphines towards the quasilinear iron(i) complex [Fe(N(SiMe<sub>3</sub>)<sub>2</sub>)<sub>2</sub>]<sup>-</sup> - between inertness, P-C bond cleavage and C-C double bond isomerisation.
Chemical communications (Cambridge, England), 2020, 56, 2268-2271
7125837 CIFC21 H25 N O3P 1 21/c 18.746; 10.239; 21.43
90; 97.29; 90		1904Wang, Bo; He, Dan; Ren, Beige; Yao, Tuanli
Synthesis of imides via palladium-catalyzed three-component coupling of aryl halides, isocyanides and carboxylic acids.
Chemical communications (Cambridge, England), 2020, 56, 900-903
7125838 CIFC34 H31 N O2P -18.7448; 12.2039; 13.7109
71.125; 73.114; 76.737		1309.9Vrána, Jan; Samsonov, Maksim A.; Němec, Vlastimil; RůŽička, Aleš
Access to the most sterically crowded anilines via non-catalysed C-C coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 2487-2490
7125839 CIFC35 H30.5 N O2.5P 1 21/c 116.515; 6.8442; 24.238
90; 105.844; 90		2635.6Vrána, Jan; Samsonov, Maksim A.; Němec, Vlastimil; RůŽička, Aleš
Access to the most sterically crowded anilines via non-catalysed C-C coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 2487-2490
7125840 CIFC43 H49 Cl2 N O2P 1 21/m 18.0461; 25.3743; 9.3223
90; 98.68; 90		1881.48Vrána, Jan; Samsonov, Maksim A.; Němec, Vlastimil; RůŽička, Aleš
Access to the most sterically crowded anilines via non-catalysed C-C coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 2487-2490
7125841 CIFC34 H31 NP -110.694; 14.5078; 16.6117
96.571; 104.496; 90.146		2477.5Vrána, Jan; Samsonov, Maksim A.; Němec, Vlastimil; RůŽička, Aleš
Access to the most sterically crowded anilines via non-catalysed C-C coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 2487-2490
7125842 CIFC56 H59 NA e a 215.828; 16.995; 16.819
90; 90; 90		4524Vrána, Jan; Samsonov, Maksim A.; Němec, Vlastimil; RůŽička, Aleš
Access to the most sterically crowded anilines via non-catalysed C-C coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 2487-2490
7125843 CIFC42 H47 NP -16.3152; 10.7638; 24.7246
85.9667; 87.0612; 88.1823		1673.63Vrána, Jan; Samsonov, Maksim A.; Němec, Vlastimil; RůŽička, Aleš
Access to the most sterically crowded anilines via non-catalysed C-C coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 2487-2490
7125844 CIFC45 H37 Cl2 NP 1 21/m 18.755; 20.6545; 9.7582
90; 106.074; 90		1695.59Vrána, Jan; Samsonov, Maksim A.; Němec, Vlastimil; RůŽička, Aleš
Access to the most sterically crowded anilines via non-catalysed C-C coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 2487-2490
7125845 CIFC68 H83 NC 1 2/c 119.1224; 13.9671; 20.7356
90; 93.252; 90		5529.2Vrána, Jan; Samsonov, Maksim A.; Němec, Vlastimil; RůŽička, Aleš
Access to the most sterically crowded anilines via non-catalysed C-C coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 2487-2490
7125846 CIFC40 H43 N O2P -110.3051; 12.5154; 13.8322
73.95; 68.779; 80.981		1594.98Vrána, Jan; Samsonov, Maksim A.; Němec, Vlastimil; RůŽička, Aleš
Access to the most sterically crowded anilines via non-catalysed C-C coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 2487-2490
7125847 CIFC40 H44 F4 N12 O21 S5P -112.8294; 12.9628; 17.3033
81.9569; 83.7579; 84.127		2821.31Lavaud, Lucien; Azarias, Cloé; Canard, Gabriel; Pascal, Simon; Galiana, Joachim; Giorgi, Michel; Chen, Zhongrui; Jacquemin, Denis; Siri, Olivier
Fused bis-azacalixphyrin that reaches NIR-II absorptions.
Chemical communications (Cambridge, England), 2020, 56, 896-899
7125848 CIFC37 H47 N10 O8P -110.993; 12.9694; 14.3295
94.206; 106.083; 103.833		1884.65Lavaud, Lucien; Azarias, Cloé; Canard, Gabriel; Pascal, Simon; Galiana, Joachim; Giorgi, Michel; Chen, Zhongrui; Jacquemin, Denis; Siri, Olivier
Fused bis-azacalixphyrin that reaches NIR-II absorptions.
Chemical communications (Cambridge, England), 2020, 56, 896-899
7125849 CIFC27 H38 B Cl N6 NiP 1 21/n 19.6383; 17.821; 16.177
90; 91.925; 90		2777.1Hill, Ethan A.; Zhao, Norman; Filatov, Alexander S.; Anderson, John S.
Nickel(ii)-methyl complexes adopting unusual seesaw geometries.
Chemical communications (Cambridge, England), 2020, 56, 7861-7864
7125850 CIFC46 H59 B N6 NiI 41/a :234.481; 34.481; 13.9826
90; 90; 90		16624Hill, Ethan A.; Zhao, Norman; Filatov, Alexander S.; Anderson, John S.
Nickel(ii)-methyl complexes adopting unusual seesaw geometries.
Chemical communications (Cambridge, England), 2020, 56, 7861-7864
7125851 CIFC154 H396 N72 Na2 Ni37.99 O280 P6 S6 W58.01C 1 2/m 123.311; 39.04; 27.663
90; 106.026; 90		24197Wang, Sa-Sa; Yang, Wen-Bin; Yang, Mingxue; Wu, Xiao-Yuan; Wu, Weiming; Wang, Song-Xia; Lin, Lang; Lu, Can-Zhong
A bi-polyoxometallate-based host-guest metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 2503-2506
7125852 CIFC23 H57 N11 Ni7 O43 P W9P 21 21 2113.4978; 14.1387; 35.9568
90; 90; 90		6862Wang, Sa-Sa; Yang, Wen-Bin; Yang, Mingxue; Wu, Xiao-Yuan; Wu, Weiming; Wang, Song-Xia; Lin, Lang; Lu, Can-Zhong
A bi-polyoxometallate-based host-guest metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 2503-2506
7125853 CIFC23 H58 N10 Ni7 O43 P W9P 21 21 2113.4578; 14.1507; 36.0116
90; 90; 90		6858Wang, Sa-Sa; Yang, Wen-Bin; Yang, Mingxue; Wu, Xiao-Yuan; Wu, Weiming; Wang, Song-Xia; Lin, Lang; Lu, Can-Zhong
A bi-polyoxometallate-based host-guest metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 2503-2506
7125854 CIFC23 H60 N10 Ni7 O45 P W9P 21 21 2113.5091; 14.2789; 36.111
90; 90; 90		6965.63Wang, Sa-Sa; Yang, Wen-Bin; Yang, Mingxue; Wu, Xiao-Yuan; Wu, Weiming; Wang, Song-Xia; Lin, Lang; Lu, Can-Zhong
A bi-polyoxometallate-based host-guest metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 2503-2506
7125855 CIFC16 H17 F5 Si2P -17.7407; 9.4632; 13.1078
74.013; 80.178; 67.671		851.47Linnemannstöns, Marvin; Schwabedissen, Jan; Schultz, Aaron A.; Neumann, Beate; Stammler, Hans-Georg; Berger, Raphael J. F.; Mitzel, Norbert W.
London dispersion-driven hetero-aryl-aryl interactions in 1,2-diaryldisilanes.
Chemical communications (Cambridge, England), 2020, 56, 2252-2255
7125856 CIFC16 H12 Cl5 F5 Si2P -17.4433; 15.7582; 18.0844
89.433; 81.593; 80.33		2068.3Linnemannstöns, Marvin; Schwabedissen, Jan; Schultz, Aaron A.; Neumann, Beate; Stammler, Hans-Georg; Berger, Raphael J. F.; Mitzel, Norbert W.
London dispersion-driven hetero-aryl-aryl interactions in 1,2-diaryldisilanes.
Chemical communications (Cambridge, England), 2020, 56, 2252-2255
7125857 CIFC16 H17 Cl5 Si2P -19.0639; 9.3355; 13.4071
94.436; 104.175; 113.509		988.88Linnemannstöns, Marvin; Schwabedissen, Jan; Schultz, Aaron A.; Neumann, Beate; Stammler, Hans-Georg; Berger, Raphael J. F.; Mitzel, Norbert W.
London dispersion-driven hetero-aryl-aryl interactions in 1,2-diaryldisilanes.
Chemical communications (Cambridge, England), 2020, 56, 2252-2255
7125858 CIFC16 H12 Cl5 F5 Si2P 1 21/n 17.5524; 14.9892; 18.806
90; 101.387; 90		2087.02Linnemannstöns, Marvin; Schwabedissen, Jan; Schultz, Aaron A.; Neumann, Beate; Stammler, Hans-Georg; Berger, Raphael J. F.; Mitzel, Norbert W.
London dispersion-driven hetero-aryl-aryl interactions in 1,2-diaryldisilanes.
Chemical communications (Cambridge, England), 2020, 56, 2252-2255
7125859 CIFC16 H12 Cl5 F5 Si2P 1 21/n 17.461; 19.0631; 14.6867
90; 91.567; 90		2088.11Linnemannstöns, Marvin; Schwabedissen, Jan; Schultz, Aaron A.; Neumann, Beate; Stammler, Hans-Georg; Berger, Raphael J. F.; Mitzel, Norbert W.
London dispersion-driven hetero-aryl-aryl interactions in 1,2-diaryldisilanes.
Chemical communications (Cambridge, England), 2020, 56, 2252-2255
7125860 CIFC87 H39 N3 Ni3 O39 Tb3R -3 m :H47.989; 47.989; 13.297
90; 90; 120		26520Chen, Hongtai; Zhuang, Gui-Lin; Fan, Liming; Zhang, Xiutang; Gao, Lin-Na; Sun, Di
A highly robust heterometallic Tb<sup>III</sup>/Ni<sup>II</sup>-organic framework for C<sub>2</sub> hydrocarbon separation and capture.
Chemical communications (Cambridge, England), 2020, 56, 2047-2050
7125861 CIFC6 N15 O3C 1 2/c 116.6224; 11.4096; 12.9021
90; 97.1063; 90		2428.15Foroughi, Leila M.; Wiscons, Ren A.; Du Bois, Derek R.; Matzger, Adam J.
Improving stability of the metal-free primary energetic cyanuric triazide (CTA) through cocrystallization.
Chemical communications (Cambridge, England), 2020, 56, 2111-2114
7125862 CIFC6 N15 O3C 1 2/c 117.0625; 11.4704; 13.02
90; 97.727; 90		2525.1Foroughi, Leila M.; Wiscons, Ren A.; Du Bois, Derek R.; Matzger, Adam J.
Improving stability of the metal-free primary energetic cyanuric triazide (CTA) through cocrystallization.
Chemical communications (Cambridge, England), 2020, 56, 2111-2114
7125863 CIFC20 H21 N O2C 1 2 114.3043; 9.7587; 12.3878
90; 105.846; 90		1663.5Deng, Xiong-Fei; Wang, Ying-Wei; Zhang, Shi-Qi; Li, Ling; Li, Guang-Xun; Zhao, Gang; Tang, Zhuo
An organocatalytic asymmetric Friedel-Crafts reaction of 2-substituted indoles with aldehydes: enantioselective synthesis of α-hydroxyl ketones by low loading of chiral phosphoric acid.
Chemical communications (Cambridge, England), 2020, 56, 2499-2502
7125864 CIFC42 H38 N6 O4 Zn2C 1 2 120.4932; 25.8736; 9.652
90; 99.109; 90		5053.3Ma, Xue; Zhang, Yanhao; Gao, Yu; Li, Xinglin; Wang, Cuijie; Yuan, Hang; Yu, Ajuan; Zhang, Shusheng; Cui, Yuanyuan
Revelation of the chiral recognition of alanine and leucine in an l-phenylalanine-based metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 1034-1037
7125865 CIFC15 H16 N2 O3P 1 21/c 112.777; 5.986; 17.896
90; 93.909; 90		1365.6Satyam, Killari; Harish, Battu; Nanubolu, Jagadeesh Babu; Suresh, Surisetti
N-Heterocyclic carbene (NHC)-catalyzed tandem imine umpolung-aza-Michael addition-oxidation of β-carboline cyclic imines.
Chemical communications (Cambridge, England), 2020, 56, 2803-2806
7125866 CIFC26 H18 Cl2 O5P 1 21/c 110.613; 23.82; 19.202
90; 105.61; 90		4675Feng, Shumin; Gong, Shengyi; Feng, Guoqiang
Aggregation-induced emission and solid fluorescence of fluorescein derivatives.
Chemical communications (Cambridge, England), 2020, 56, 2511-2513
7125867 CIFC22 H16 O5P n a 218.5365; 10.915; 18.183
90; 90; 90		1694.2Feng, Shumin; Gong, Shengyi; Feng, Guoqiang
Aggregation-induced emission and solid fluorescence of fluorescein derivatives.
Chemical communications (Cambridge, England), 2020, 56, 2511-2513
7125868 CIFC18 H12 N2 S8P 1 21/c 113.6086; 12.8562; 11.7791
90; 97.382; 90		2043.73Bechu, Damien; Xie, Lilia S.; Le Breton, Nolwenn; Choua, Sylvie; Dincă, Mircea; Hosseini, Mir Wais; Baudron, Stéphane A
Interdigitated conducting tetrathiafulvalene-based coordination networks.
Chemical communications (Cambridge, England), 2020, 56, 2407-2410
7125869 CIFC41 H27 Cl9 Fe N6 S18C 1 2/c 136.701; 9.6026; 20.217
90; 121.187; 90		6095.3Bechu, Damien; Xie, Lilia S.; Le Breton, Nolwenn; Choua, Sylvie; Dincă, Mircea; Hosseini, Mir Wais; Baudron, Stéphane A
Interdigitated conducting tetrathiafulvalene-based coordination networks.
Chemical communications (Cambridge, England), 2020, 56, 2407-2410
7125870 CIFC41 H27 Cl9 Co N6 S18C 1 2/c 136.6636; 9.568; 20.1665
90; 121.372; 90		6040.1Bechu, Damien; Xie, Lilia S.; Le Breton, Nolwenn; Choua, Sylvie; Dincă, Mircea; Hosseini, Mir Wais; Baudron, Stéphane A
Interdigitated conducting tetrathiafulvalene-based coordination networks.
Chemical communications (Cambridge, England), 2020, 56, 2407-2410
7125871 CIFC18 H17 N O2 SP 1 21/n 114.5594; 12.0737; 18.6579
90; 103.921; 90		3183.5Qian, Lei-Lei; Min, Xiang-Ting; Hu, Yan-Cheng; Shen, Bing-Xue; Yang, Sa-Na; Wan, Boshun; Chen, Qing-An
Ruthenium(ii)-catalyzed intermolecular annulation of alkenyl sulfonamides with alkynes: access to bicyclic sultams.
Chemical communications (Cambridge, England), 2020, 56, 2614-2617
7125872 CIFC22 H38 Cl2 N6 O7 PtP -112.7146; 15.4589; 16.874
90.091; 111.105; 99.087		3049.2Shu, Liwei; Ren, Lulu; Wang, Yuchen; Fang, Tao; Ye, Zhijian; Han, Weidong; Chen, Chao; Wang, Hangxiang
Niacin-ligated platinum(iv)-ruthenium(ii) chimeric complexes synergistically suppress tumor metastasis and growth with potentially reduced toxicity in vivo.
Chemical communications (Cambridge, England), 2020, 56, 3069-3072
7125873 CIFC34 H34 Dy3 O22C 1 2/c 124.294; 18.1452; 22.5707
90; 105.538; 90		9585.98Zhong, Li; Chen, Wen-Bin; OuYang, Zhi-Jian; Yang, Meng; Zhang, Yi-Quan; Gao, Song; Schulze, Michael; Wernsdorfer, Wolfgang; Dong, Wen
Unprecedented one-dimensional chain and two-dimensional network dysprosium(iii) single-molecule toroics with white-light emission.
Chemical communications (Cambridge, England), 2020, 56, 2590-2593
7125874 CIFC48 H56 Dy6 O36P -115.0529; 16.5502; 19.5506
66.985; 74.839; 78.055		4296.7Zhong, Li; Chen, Wen-Bin; OuYang, Zhi-Jian; Yang, Meng; Zhang, Yi-Quan; Gao, Song; Schulze, Michael; Wernsdorfer, Wolfgang; Dong, Wen
Unprecedented one-dimensional chain and two-dimensional network dysprosium(iii) single-molecule toroics with white-light emission.
Chemical communications (Cambridge, England), 2020, 56, 2590-2593
7125875 CIFC47 H81 N5 O6P 1 21/n 114.0335; 19.5712; 18.2778
90; 100.406; 90		4937.5Turner, Nicholas A.; Freeman, Matthew B.; Pratt, Harry D.; Crockett, Austin E.; Jones, Daniel S.; Anstey, Mitchell R.; Anderson, Travis M.; Bejger, Christopher M.
Desymmetrized hexasubstituted [3]radialene anions as aqueous organic catholytes for redox flow batteries.
Chemical communications (Cambridge, England), 2020, 56, 2739-2742
7125876 CIFC46 H78 N6 O4P 1 21/n 119.7559; 12.4952; 38.3843
90; 93.145; 90		9461Turner, Nicholas A.; Freeman, Matthew B.; Pratt, Harry D.; Crockett, Austin E.; Jones, Daniel S.; Anstey, Mitchell R.; Anderson, Travis M.; Bejger, Christopher M.
Desymmetrized hexasubstituted [3]radialene anions as aqueous organic catholytes for redox flow batteries.
Chemical communications (Cambridge, England), 2020, 56, 2739-2742
7125877 CIFC21 H16 Cl N3 O4P 1 21 19.314; 21.8053; 9.5831
90; 94.306; 90		1940.78Ge, Zhen-Zhen; Yang, Lei; You, Yong; Wang, Zhen-Hua; Xie, Ke-Xin; Zhou, Ming-Qiang; Zhao, Jian-Qiang; Yuan, Wei-Cheng
Asymmetric dearomatization of 2-nitrobenzofurans by organocatalyzed one-step Michael addition to access 3,3'-disubstituted oxindoles.
Chemical communications (Cambridge, England), 2020, 56, 2586-2589
7125878 CIFC349.68 H478.7 Ag18 O29.68 P8 S17P 4/n c c :226.6947; 26.6947; 50.0946
90; 90; 90		35697.8Tian, Fan; Chen, Rong
Ag<sub>18</sub>(μ<sub>8</sub>-S)(p-TBBT)<sub>16</sub>(PPh<sub>3</sub>)<sub>8</sub>: symmetry breaking induced by the core to generate chirality.
Chemical communications (Cambridge, England), 2020, 56, 2719-2722
7125879 CIFC21 H22 N3 O2P -16.5347; 11.4519; 14.2937
112.503; 95.468; 100.753		954.35Zhuang, Jiabao; Yang, Hanxiao; Li, Yue; Wang, Bing; Li, Nan; Zhao, Na
Efficient photosensitizers with aggregation-induced emission characteristics for lysosome- and Gram-positive bacteria-targeted photodynamic therapy.
Chemical communications (Cambridge, England), 2020, 56, 2630-2633
7125880 CIFC206 H299 N33 O21 P2C 1 2 140.8647; 28.7021; 26.5738
90; 129.6; 90		24015.7Fu, Jin; Zheng, Bo; Zhang, Huizheng; Zhao, Yanxia; Zhang, Dan; Zhang, Wenyao; Yang, Xiao-Juan; Wu, Biao
Chirality transcription in the anion-coordination-driven assembly of tetrahedral cages.
Chemical communications (Cambridge, England), 2020, 56, 2475-2478
7125881 CIFC204 H294 N32 O20 P2C 1 2 140.912; 28.685; 26.497
90; 129.742; 90		23911Fu, Jin; Zheng, Bo; Zhang, Huizheng; Zhao, Yanxia; Zhang, Dan; Zhang, Wenyao; Yang, Xiao-Juan; Wu, Biao
Chirality transcription in the anion-coordination-driven assembly of tetrahedral cages.
Chemical communications (Cambridge, England), 2020, 56, 2475-2478
7125882 CIFC87 H117 N16 O10 PP -4 2 c25.958; 25.958; 28.548
90; 90; 90		19236Fu, Jin; Zheng, Bo; Zhang, Huizheng; Zhao, Yanxia; Zhang, Dan; Zhang, Wenyao; Yang, Xiao-Juan; Wu, Biao
Chirality transcription in the anion-coordination-driven assembly of tetrahedral cages.
Chemical communications (Cambridge, England), 2020, 56, 2475-2478
7125883 CIFC33 H25 N3P 1 21/c 110.712; 26.2639; 9.6385
90; 114.352; 90		2470.4Liang, Taoyuan; Gong, Lingzhen; Zhao, He; Jiang, Huanfeng; Zhang, Min
Straightforward access to novel indolo[2,3-b]indoles via aerobic copper-catalyzed [3+2] annulation of diarylamines and indoles.
Chemical communications (Cambridge, England), 2020, 56, 2807-2810
7125884 CIFC70 H111 F3 N10 O24P 1 21 19.529; 23.743; 18.276
90; 96.35; 90		4109.5Cringoli, Maria Cristina; Romano, Chiara; Parisi, Evelina; Waddington, Lynne J.; Melchionna, Michele; Semeraro, Sabrina; De Zorzi, Rita; Grönholm, Mikaela; Marchesan, Silvia
Bioadhesive supramolecular hydrogel from unprotected, short d,l-peptides with Phe-Phe and Leu-Asp-Val motifs.
Chemical communications (Cambridge, England), 2020, 56, 3015-3018
7125885 CIFC120 H175 Eu2 F18 N21 O36 Pt2 S6C 1 2/c 120.9232; 22.2447; 36.0709
90; 104.29; 90		16269Zhu, Qiang-Yu; Zhou, Li-Peng; Cai, Li-Xuan; Li, Xiao-Zhen; Zhou, Jin; Sun, Qing-Fu
Chiral auxiliary and induced chiroptical sensing with 5d/4f lanthanide-organic macrocycles.
Chemical communications (Cambridge, England), 2020, 56, 2861-2864
7125886 CIFC174 H213 Eu2 F18 N29 O35 Pt2 S6P -113.8397; 16.9264; 21.3207
68.595; 81.719; 77.817		4532.9Zhu, Qiang-Yu; Zhou, Li-Peng; Cai, Li-Xuan; Li, Xiao-Zhen; Zhou, Jin; Sun, Qing-Fu
Chiral auxiliary and induced chiroptical sensing with 5d/4f lanthanide-organic macrocycles.
Chemical communications (Cambridge, England), 2020, 56, 2861-2864
7125887 CIFC922 H1222 N150 O268 Zn24R -3 :H51.495; 51.495; 48.469
90; 90; 120		111308Pei, Wen-Yuan; Yang, Jin; Wu, Hui; Zhou, Wei; Yang, Ying-Wei; Ma, Jian-Fang
A calix[4]resorcinarene-based giant coordination cage: controlled assembly and iodine uptake.
Chemical communications (Cambridge, England), 2020, 56, 2491-2494
7125888 CIFC30 H30 Al2 F10 N2P -18.4228; 9.8609; 10.1038
65.09; 72.958; 85.464		726.74Kysliak, Oleksandr; Görls, Helmar; Kretschmer, Robert
C-F bond activation by pentamethylcyclopentadienyl-aluminium(i): a combined experimental/computational exercise.
Chemical communications (Cambridge, England), 2020, 56, 7865-7868
7125889 CIFC32 H32 Al2 F10P 1 21/n 19.1602; 21.937; 14.8657
90; 97.288; 90		2963.09Kysliak, Oleksandr; Görls, Helmar; Kretschmer, Robert
C-F bond activation by pentamethylcyclopentadienyl-aluminium(i): a combined experimental/computational exercise.
Chemical communications (Cambridge, England), 2020, 56, 7865-7868
7125890 CIFC32 H34 Al2 F8P 1 21/n 19.1825; 10.793; 14.8825
90; 99.315; 90		1455.51Kysliak, Oleksandr; Görls, Helmar; Kretschmer, Robert
C-F bond activation by pentamethylcyclopentadienyl-aluminium(i): a combined experimental/computational exercise.
Chemical communications (Cambridge, England), 2020, 56, 7865-7868
7125891 CIFC32 H30 Al2 F12C 1 2/c 117.0235; 10.2649; 17.33
90; 94.82; 90		3017.61Kysliak, Oleksandr; Görls, Helmar; Kretschmer, Robert
C-F bond activation by pentamethylcyclopentadienyl-aluminium(i): a combined experimental/computational exercise.
Chemical communications (Cambridge, England), 2020, 56, 7865-7868
7125892 CIFC34 H30 Al2 F16P -18.4379; 9.9671; 11.3803
115.809; 98.981; 92.895		843.48Kysliak, Oleksandr; Görls, Helmar; Kretschmer, Robert
C-F bond activation by pentamethylcyclopentadienyl-aluminium(i): a combined experimental/computational exercise.
Chemical communications (Cambridge, England), 2020, 56, 7865-7868
7125893 CIFC22 H14 N4 O9 Pb2P -110.489; 11.331; 11.564
90.053; 107.913; 103.473		1267.9Liu, Jiao; Yang, Guo-Ping; Jin, Jing; Wu, Dan; Ma, Lu-Fang; Wang, Yao-Yu
A first new porous d-p HMOF material with multiple active sites for excellent CO<sub>2</sub> capture and catalysis.
Chemical communications (Cambridge, England), 2020, 56, 2395-2398
7125894 CIFC22 H14 N4 O9 Pb ZnP -110.1986; 12.074; 13.1106
112.525; 91.216; 95.011		1482.93Liu, Jiao; Yang, Guo-Ping; Jin, Jing; Wu, Dan; Ma, Lu-Fang; Wang, Yao-Yu
A first new porous d-p HMOF material with multiple active sites for excellent CO<sub>2</sub> capture and catalysis.
Chemical communications (Cambridge, England), 2020, 56, 2395-2398
7125895 CIFC20 H34 Br N O2P -14.73398; 5.65377; 38.3824
85.1193; 85.3321; 83.3811		1014.09Marczenko, Katherine M.; Chitnis, Saurabh S.
Bismuthanylstibanes.
Chemical communications (Cambridge, England), 2020, 56, 8015-8018
7125896 CIFC47 H75 Bi N4 Sb Si4P 1 21/n 111.7148; 24.8374; 17.6977
90; 98.486; 90		5093Marczenko, Katherine M.; Chitnis, Saurabh S.
Bismuthanylstibanes.
Chemical communications (Cambridge, England), 2020, 56, 8015-8018
7125897 CIFC38 H60 Bi N4 Sb Si4C 1 2/c 120.7764; 9.9748; 42.2992
90; 100.049; 90		8631.6Marczenko, Katherine M.; Chitnis, Saurabh S.
Bismuthanylstibanes.
Chemical communications (Cambridge, England), 2020, 56, 8015-8018
7125898 CIFC38 H60 Bi N4 S Sb Si4P 1 21/c 116.594; 12.7708; 21.9816
90; 108.214; 90		4424.9Marczenko, Katherine M.; Chitnis, Saurabh S.
Bismuthanylstibanes.
Chemical communications (Cambridge, England), 2020, 56, 8015-8018
7125899 CIFC44 H72 Bi N4 Sb Si4P 1 21/c 110.5482; 12.2644; 19.2011
90; 101.656; 90		2432.77Marczenko, Katherine M.; Chitnis, Saurabh S.
Bismuthanylstibanes.
Chemical communications (Cambridge, England), 2020, 56, 8015-8018
7125900 CIFC15 H15 F3 O4P 21 21 217.3643; 8.6863; 22.636
90; 90; 90		1448Terashima, Kyu; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Construction of trifluoromethylated quaternary stereocenters via p-quinone methides.
Chemical communications (Cambridge, England), 2020, 56, 3031-3034
7125901 CIFC23 H25 F3 O7P -18.6848; 9.8256; 13.1255
84.786; 88.888; 89.989		1115.2Terashima, Kyu; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Construction of trifluoromethylated quaternary stereocenters via p-quinone methides.
Chemical communications (Cambridge, England), 2020, 56, 3031-3034
7125902 CIFC28 H27 N O6 SP 21 21 219.34005; 9.81274; 26.8301
90; 90; 90		2459.02Kondo, Masaru; Wathsala, H. D. P.; Sako, Makoto; Hanatani, Yutaro; Ishikawa, Kazunori; Hara, Satoshi; Takaai, Takayuki; Washio, Takashi; Takizawa, Shinobu; Sasai, Hiroaki
Exploration of flow reaction conditions using machine-learning for enantioselective organocatalyzed Rauhut-Currier and [3+2] annulation sequence.
Chemical communications (Cambridge, England), 2020, 56, 1259-1262
7125903 CIFC36 H44 Br N O5P 110.1681; 11.5222; 15.4679
105.32; 90.967; 100.049		1717.2Eitzinger, Andreas; Winter, Michael; Schörgenhumer, Johannes; Waser, Mario
Quaternary β<sup>2,2</sup>-amino acid derivatives by asymmetric addition of isoxazolidin-5-ones to para-quinone methides.
Chemical communications (Cambridge, England), 2020, 56, 579-582
7125904 CIFC42 H49 N O5P 19.1974; 10.5189; 11.2152
66.716; 71.426; 78.998		942.12Eitzinger, Andreas; Winter, Michael; Schörgenhumer, Johannes; Waser, Mario
Quaternary β<sup>2,2</sup>-amino acid derivatives by asymmetric addition of isoxazolidin-5-ones to para-quinone methides.
Chemical communications (Cambridge, England), 2020, 56, 579-582
7125905 CIFC19 H26 O3C 1 2 117.2464; 7.0762; 28.17
90; 103.591; 90		3341.57Shi, Linlin; He, Yingdong; Gong, Jianxian; Yang, Zhen
Concise gram-scale synthesis of Euphorikanin A skeleton through a domino ring-closing metathesis strategy.
Chemical communications (Cambridge, England), 2020, 56, 531-534
7125906 CIFC60 H57 N3 O6P 21 21 219.94998; 15.8783; 31.7019
90; 90; 90		5008.54Lu, Fo-Yun; Chen, Yu-Jue; Chen, Yuan; Ding, Xuan; Guan, Zhi; He, Yan-Hong
Highly enantioselective electrosynthesis of C2-quaternary indolin-3-ones.
Chemical communications (Cambridge, England), 2020, 56, 623-626
7125907 CIFC20 H17.27 Cl N O2P 21 21 2110.0005; 15.089; 23.6172
90; 90; 90		3563.78Lu, Fo-Yun; Chen, Yu-Jue; Chen, Yuan; Ding, Xuan; Guan, Zhi; He, Yan-Hong
Highly enantioselective electrosynthesis of C2-quaternary indolin-3-ones.
Chemical communications (Cambridge, England), 2020, 56, 623-626
7125908 CIFC65.96 H95.17 Br0.76 Mg2 O12C 1 2/c 120.51; 12.667; 26.498
90; 108.671; 90		6522Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125909 CIFC186 H228 O33C 1 2/c 140.636; 12.2639; 36.165
90; 113.845; 90		16485Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125910 CIFC67.57 H98.78 Br0.36 Mg2 O12P 1 21 113.565; 12.45; 20.554
90; 107.915; 90		3302.9Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125911 CIFC72.34 H107.54 Br0.14 Mg2 O12P -111.959; 13.536; 22.775
75.943; 88.27; 73.195		3420Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125912 CIFC251.55 H351.03 Br0.06 Mg4 O44P -114.01; 17.806; 25.7096
95.703; 103.75; 102.801		5996.2Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125913 CIFC69 H101 Mg2 O12P 1 21/c 113.392; 21.18; 23.936
90; 96.985; 90		6739Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125914 CIFC122 H165 Br2 Mg2 O24P 1 21/c 111.973; 26.293; 39.008
90; 97.456; 90		12176Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125915 CIFC39 H0 Ce N11 O0 S7P m -3 m11.3981; 11.3981; 11.3981
90; 90; 90		1480.8Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125916 CIFC39 H0 Lu N11 O0 S7I 4/m m m11.3929; 11.3929; 22.386
90; 90; 90		2905.7Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125917 CIFC39 H0 Gd N11 O S7I 4/m m m11.418; 11.418; 22.504
90; 90; 90		2933.9Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125918 CIFC39 H0 N11 O0 Pr S7P m -3 m11.4242; 11.4242; 11.4242
90; 90; 90		1491Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125919 CIFC39 H0 N11 O0 S7 TbI 4/m m m11.3933; 11.3933; 22.4759
90; 90; 90		2917.5Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125920 CIFC39 H0 Eu N11 S7I 4/m m m11.3876; 11.3876; 22.5539
90; 90; 90		2924.7Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125921 CIFC39 H0 La N11 O0 S7P m -3 m11.4263; 11.4263; 11.4263
90; 90; 90		1491.82Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125922 CIFC39 Am N11 S7P m -3 m11.3641; 11.3641; 11.3641
90; 90; 90		1467.6Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125923 CIFC39 H0 N11 Nd O0 S7P m -3 m11.3976; 11.3976; 11.3976
90; 90; 90		1480.61Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125924 CIFC39 H0 Ho N11 O0 S7I 4/m m m11.4039; 11.4039; 22.5714
90; 90; 90		2935.39Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125925 CIFC39 H0 N11 O0 S7 TmI 4/m m m11.3875; 11.3875; 22.478
90; 90; 90		2914.8Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125926 CIFC39 H0 Dy N11 O0 S7I 4/m m m11.4134; 11.4134; 22.6144
90; 90; 90		2945.9Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125927 CIFC39 H0 Er N11 O0 S7I 4/m m m11.4093; 11.4093; 22.577
90; 90; 90		2938.9Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125928 CIFC39 H0 N11 O0 S7 SmP m -3 m11.3772; 11.3772; 11.3772
90; 90; 90		1472.67Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125929 CIFC39 H0 N11 O0 S7 YbI 4/m m m11.3736; 11.3736; 22.495
90; 90; 90		2909.93Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125930 CIFC39 H0 Cm N11 O3 S7P m -3 m11.3752; 11.3752; 11.3752
90; 90; 90		1471.9Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125931 CIFC60 H80 B2 F4 I4 N4 O23 V6P 1 21 110.02302; 22.8571; 15.9505
90; 91.5838; 90		3652.82Gu, Yaqi; Li, Qi; Huang, Yichao; Zhu, Yingting; Wei, Yongge; Ruhlmann, Laurent
Polyoxovanadate-iodobodipy supramolecular assemblies: new agents for high efficiency cancer photochemotherapy.
Chemical communications (Cambridge, England), 2020, 56, 2869-2872
7125932 CIFC38 H26 O5 S2C 1 2/c 118.6651; 9.1102; 18.3035
90; 108.224; 90		2956.26Zeng, Linwei; Chen, Renjie; Zhang, Chen; Xie, Hujun; Cui, Sunliang
Iridium(i)-catalyzed hydration/esterification of 2-alkynylphenols and carboxylic acids.
Chemical communications (Cambridge, England), 2020, 56, 3093-3096
7125933 CIFC21 H14 N2 O7P -16.914; 10.6; 13.029
99.77; 96.31; 92.38		933.6Zeng, Linwei; Chen, Renjie; Zhang, Chen; Xie, Hujun; Cui, Sunliang
Iridium(i)-catalyzed hydration/esterification of 2-alkynylphenols and carboxylic acids.
Chemical communications (Cambridge, England), 2020, 56, 3093-3096
7125934 CIFC21 H15 N O5P -111.02; 11.052; 16.364
106.83; 104.08; 100.237		1783Zeng, Linwei; Chen, Renjie; Zhang, Chen; Xie, Hujun; Cui, Sunliang
Iridium(i)-catalyzed hydration/esterification of 2-alkynylphenols and carboxylic acids.
Chemical communications (Cambridge, England), 2020, 56, 3093-3096
7125935 CIFC16 H16 N2C 1 2/c 120.126; 7.6043; 19.1043
90; 114.182; 90		2667.2Roy, Subhra Kanti; Purkait, Anisha; Aziz, Sk Md Tarik; Jana, Chandan K.
Acid mediated coupling of aliphatic amines and nitrosoarenes to indoles.
Chemical communications (Cambridge, England), 2020, 56, 3167-3170
7125936 CIFC15 H14 N2P c c n20.3252; 17.4919; 7.6118
90; 90; 90		2706.2Roy, Subhra Kanti; Purkait, Anisha; Aziz, Sk Md Tarik; Jana, Chandan K.
Acid mediated coupling of aliphatic amines and nitrosoarenes to indoles.
Chemical communications (Cambridge, England), 2020, 56, 3167-3170
7125937 CIFC30 H42 O3P 21 21 217.6085; 18.276; 18.693
90; 90; 90		2599.3Wang, Wen-Li; Liu, Xiao-Qin; Zhang, Mei-Hui; Lin, Bin; Zhu, Dong-Rong; Li, Ling-Nan; Chen, Chen; Han, Chao; Luo, Jian-Guang; Kong, Ling-Yi
Taxodisones A and B: bioactive C<sub>30</sub>-terpenes with new skeletons from Taxodium distichum and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 3329-3332
7125938 CIFC30 H42 O3P 1 21 110.264; 12.5469; 20.5284
90; 101.807; 90		2587.74Wang, Wen-Li; Liu, Xiao-Qin; Zhang, Mei-Hui; Lin, Bin; Zhu, Dong-Rong; Li, Ling-Nan; Chen, Chen; Han, Chao; Luo, Jian-Guang; Kong, Ling-Yi
Taxodisones A and B: bioactive C<sub>30</sub>-terpenes with new skeletons from Taxodium distichum and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 3329-3332
7125939 CIFC76 H74 Cl2 Cr2 F10 N4P -115.8112; 18.2465; 23.607
78.927; 87.544; 81.311		6606.4Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125940 CIFC44 H50 Cr F8 N2 O5 SP -111.3653; 17.4031; 21.1322
93.966; 102.004; 96.269		4045.7Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125941 CIFC54 H67 Cr F5 N3 OP -111.4314; 13.7772; 15.3492
104.593; 91.816; 93.766		2331.44Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125942 CIFC59 H70 Cr F5 N4P b c a15.3902; 22.0785; 29.9364
90; 90; 90		10172.2Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125943 CIFC44 H45 Cl Cr F5 N3P 1 21/c 118.229; 20.427; 10.3857
90; 105.421; 90		3728Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125944 CIFC49 H53 Cr F8 N3 O4 SP 1 21 117.0256; 17.8637; 17.9461
90; 112.061; 90		5058.5Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125945 CIFC360 H312 N58 O90 Pd6 S12P -126.739; 26.793; 29.537
64.09; 77.3; 86.34		18556Lee, Haeri; Kim, Dongwon; Oh, Hyejin; Jung, Ok-Sang
Molecular balloon, Pd<sub>6</sub>L<sub>8</sub> cages: recognition of alkyl sulfate surfactants.
Chemical communications (Cambridge, England), 2020, 56, 2841-2844
7125946 CIFC396 H378 N48 O78 Pd6 S12R -3 :H29.802; 29.802; 68.496
90; 90; 120		52685Lee, Haeri; Kim, Dongwon; Oh, Hyejin; Jung, Ok-Sang
Molecular balloon, Pd<sub>6</sub>L<sub>8</sub> cages: recognition of alkyl sulfate surfactants.
Chemical communications (Cambridge, England), 2020, 56, 2841-2844
7125947 CIFC336 H240 N48 O48 Pd6I 4/m35.325; 35.325; 49.962
90; 90; 90		62345Lee, Haeri; Kim, Dongwon; Oh, Hyejin; Jung, Ok-Sang
Molecular balloon, Pd<sub>6</sub>L<sub>8</sub> cages: recognition of alkyl sulfate surfactants.
Chemical communications (Cambridge, England), 2020, 56, 2841-2844
7125948 CIFC420 H426 N48 O78 Pd6 S12R -3 :H29.879; 29.879; 68.309
90; 90; 120		52813Lee, Haeri; Kim, Dongwon; Oh, Hyejin; Jung, Ok-Sang
Molecular balloon, Pd<sub>6</sub>L<sub>8</sub> cages: recognition of alkyl sulfate surfactants.
Chemical communications (Cambridge, England), 2020, 56, 2841-2844
7125949 CIFC8 H9 N OP -16.5511; 6.9192; 8.0265
93.73; 102.78; 91.769		353.68Zhai, Shengxian; Zhang, Xinping; Cheng, Bin; Li, Hui; Li, Yuntong; He, Yixuan; Li, Yun; Wang, Taimin; Zhai, Hongbin
Synthesis of tetrasubstituted thiophenes via a [3+2] cascade cyclization reaction of pyridinium 1,4-zwitterionic thiolates and activated allenes.
Chemical communications (Cambridge, England), 2020, 56, 3085-3088
7125950 CIFC22 H16 O5 SP 1 21/c 118.903; 7.1434; 14.656
90; 100.898; 90		1943.3Zhai, Shengxian; Zhang, Xinping; Cheng, Bin; Li, Hui; Li, Yuntong; He, Yixuan; Li, Yun; Wang, Taimin; Zhai, Hongbin
Synthesis of tetrasubstituted thiophenes via a [3+2] cascade cyclization reaction of pyridinium 1,4-zwitterionic thiolates and activated allenes.
Chemical communications (Cambridge, England), 2020, 56, 3085-3088
7125951 CIFC25 H28 B Br Cl2 N6 O2 WP 1 21/c 116.371; 10.3034; 17.1373
90; 94.539; 90		2881.6Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125952 CIFC50 H52 B2 N12 O4 W2P 1 21/c 113.8341; 10.1106; 20.5773
90; 106.771; 90		2755.75Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125953 CIFC72 H108 B2 N12 O4 W2P 1 21/c 113.2449; 18.7892; 16.1898
90; 107.336; 90		3846Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125954 CIFC34 H34 B N7 O2 WP 1 21/n 110.2667; 23.1598; 13.5771
90; 92.406; 90		3225.4Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125955 CIFC32.5 H32 B Cl N6 O2 WI 1 2/a 137.593; 10.4555; 32.1962
90; 96.483; 90		12573.9Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125956 CIFC28 H29 B N6 O2 WP 1 21/c 17.9501; 17.9153; 19.455
90; 100.437; 90		2725.1Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125957 CIFC28 H29 B N6 O2 WP 1 21/n 17.9431; 17.7548; 19.9617
90; 99.821; 90		2773.9Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125958 CIFC106 H130 B4 N24 O8 W4I 1 2/m 123.8078; 25.26; 25.4589
90; 114.84; 90		13894.1Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125959 CIFC60 H69 B3 N18 O6 W3P 1 21/n 114.1626; 36.3631; 14.8716
90; 90.019; 90		7658.8Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125960 CIFC26 H32 N4P b c n14.844; 9.534; 16.867
90; 90; 90		2387Wang, Wenqing; Tan, Gengwen; Feng, Rui; Fang, Yong; Chen, Chao; Ruan, Huapeng; Zhao, Yue; Wang, Xinping
Stable, yet "naked", azo radical anion ArNNAr<sup>-</sup> and dianion ArNNAr<sup>2-</sup> (Ar = 4-CN-2,6-<sup>i</sup>Pr<sub>2</sub>-C<sub>6</sub>H<sub>2</sub>) with selective CO<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 3285-3288
7125961 CIFC42 H64 N4 Na O4C 1 2/c 118.399; 14.6911; 15.7048
90; 103.277; 90		4131.6Wang, Wenqing; Tan, Gengwen; Feng, Rui; Fang, Yong; Chen, Chao; Ruan, Huapeng; Zhao, Yue; Wang, Xinping
Stable, yet "naked", azo radical anion ArNNAr<sup>-</sup> and dianion ArNNAr<sup>2-</sup> (Ar = 4-CN-2,6-<sup>i</sup>Pr<sub>2</sub>-C<sub>6</sub>H<sub>2</sub>) with selective CO<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 3285-3288
7125962 CIFC42 H64 K N4 O4C 1 2/c 118.731; 15.129; 15.467
90; 104.882; 90		4236Wang, Wenqing; Tan, Gengwen; Feng, Rui; Fang, Yong; Chen, Chao; Ruan, Huapeng; Zhao, Yue; Wang, Xinping
Stable, yet "naked", azo radical anion ArNNAr<sup>-</sup> and dianion ArNNAr<sup>2-</sup> (Ar = 4-CN-2,6-<sup>i</sup>Pr<sub>2</sub>-C<sub>6</sub>H<sub>2</sub>) with selective CO<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 3285-3288
7125963 CIFC112 H184 K4 N8 O27P -113.5116; 14.2386; 17.4578
84.41; 68.71; 86.045		3112.5Wang, Wenqing; Tan, Gengwen; Feng, Rui; Fang, Yong; Chen, Chao; Ruan, Huapeng; Zhao, Yue; Wang, Xinping
Stable, yet "naked", azo radical anion ArNNAr<sup>-</sup> and dianion ArNNAr<sup>2-</sup> (Ar = 4-CN-2,6-<sup>i</sup>Pr<sub>2</sub>-C<sub>6</sub>H<sub>2</sub>) with selective CO<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 3285-3288
7125964 CIFC64 H104 K2 N4 O19P 1 21/n 112.996; 26.8623; 22.322
90; 101.922; 90		7624.6Wang, Wenqing; Tan, Gengwen; Feng, Rui; Fang, Yong; Chen, Chao; Ruan, Huapeng; Zhao, Yue; Wang, Xinping
Stable, yet "naked", azo radical anion ArNNAr<sup>-</sup> and dianion ArNNAr<sup>2-</sup> (Ar = 4-CN-2,6-<sup>i</sup>Pr<sub>2</sub>-C<sub>6</sub>H<sub>2</sub>) with selective CO<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 3285-3288
7125965 CIFC79 H191.2 N24 O74.1 P6C 1 2/c 149.267; 14.9082; 39.726
90; 100.616; 90		28679Pramanik, Subhamay; Day, Victor W.; Bowman-James, Kristin
Supramolecular traps for highly phosphorylated inositol sources of phosphorus.
Chemical communications (Cambridge, England), 2020, 56, 3269-3272
7125966 CIFC82 H171.4 N26 O59.6 P6R -3 :H18.3819; 18.3819; 35.5789
90; 90; 120		10411.3Pramanik, Subhamay; Day, Victor W.; Bowman-James, Kristin
Supramolecular traps for highly phosphorylated inositol sources of phosphorus.
Chemical communications (Cambridge, England), 2020, 56, 3269-3272
7125967 CIFC36 H56 N12 O10P -110.6732; 12.999; 16.3255
75.5241; 85.8338; 71.3608		2078Pramanik, Subhamay; Day, Victor W.; Bowman-James, Kristin
Supramolecular traps for highly phosphorylated inositol sources of phosphorus.
Chemical communications (Cambridge, England), 2020, 56, 3269-3272
7125968 CIFC100 H50 Cu10 N20P -110.3306; 12.1908; 16.1323
92.418; 107.283; 91.169		1937.06Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125969 CIFC110 H50 Cu10 N20P -110.8822; 12.4297; 16.2388
96.008; 108.765; 90.917		2065.44Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125970 CIFC100 H50 Cu10 N20C 1 2/m 110.3986; 30.8174; 12.2534
90; 91.742; 90		3924.88Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125971 CIFC110 H50 Cu10 N20P -110.8776; 12.4524; 16.2822
95.7; 108.748; 91.392		2074.41Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125972 CIFC100 H50 Cu10 N20P -110.3877; 12.2263; 16.1951
90.741; 107.985; 91.592		1955.07Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125973 CIFC110 H50 Cu10 N20P -116.3006; 16.5127; 16.5388
98.05; 98.473; 108.223		4099.39Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125974 CIFC100 H50 Cu10 N20C 1 2/m 110.4531; 30.8052; 12.2818
90; 91.966; 90		3952.53Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125975 CIFC110 H50 Cu10 N20P -116.2846; 16.3744; 16.5641
98.035; 98.566; 108.306		4063.83Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125976 CIFC90 H82 F24 N18 P4P 42 21 219.429; 19.429; 12.057
90; 90; 90		4551.3Nian, Hao; Li, Aisen; Li, Yawen; Cheng, Lin; Wang, Ling; Xu, Weiqing; Cao, Liping
Tetraphenylethene-based tetracationic dicyclophanes: synthesis, mechanochromic luminescence, and photochemical reactions.
Chemical communications (Cambridge, England), 2020, 56, 3195-3198
7125977 CIFC61.5 H74 Cl4 N8 O7.5P -111.8059; 14.764; 19.268
78.553; 73.274; 75		3078.7Nian, Hao; Li, Aisen; Li, Yawen; Cheng, Lin; Wang, Ling; Xu, Weiqing; Cao, Liping
Tetraphenylethene-based tetracationic dicyclophanes: synthesis, mechanochromic luminescence, and photochemical reactions.
Chemical communications (Cambridge, England), 2020, 56, 3195-3198
7125978 CIFC61 H92 F6 Fe N4 O12 S2P 42 21 228.876; 28.876; 11.5084
90; 90; 90		9596Wang, Fang; Feng, Lili; Dong, Shunxi; Liu, Xiaohua; Feng, Xiaoming
Chiral N,N'-dioxide-iron(iii)-catalyzed asymmetric sulfoxidation with hydrogen peroxide.
Chemical communications (Cambridge, England), 2020, 56, 3233-3236
7125979 CIFC27.5 H44.5 Br Cr N4 O14.25P -19.8426; 12.5393; 16.1571
75.374; 79.253; 72.06		1822.8Ruan, Wenqing; Mao, Jiatao; Yang, Shida; Shi, Chuan; Jia, Guochen; Chen, Qing
Designing Cr complexes for a neutral Fe-Cr redox flow battery.
Chemical communications (Cambridge, England), 2020, 56, 3171-3174
7125980 CIFB4 Ba F6 H4 O6C 1 2/m 16.803; 7.008; 9.588
90; 92.96; 90		456.5Gai, Minqiang; Wang, Ying; Tong, Tinghao; Wang, Liying; Yang, Zhihua; Zhou, Xin; Pan, Shilie
Ba(B<sub>2</sub>OF<sub>3</sub>(OH)<sub>2</sub>)<sub>2</sub> with well-ordered OH/F anions and a unique B<sub>2</sub>OF<sub>3</sub>(OH)<sub>2</sub> dimer.
Chemical communications (Cambridge, England), 2020, 56, 3301-3304
7125981 CIFC30 H23 N3 O2 SP 21 21 2110.313; 14.7947; 15.8422
90; 90; 90		2417.17Ni, Qijian; Wang, Xuyang; Xu, Fangfang; Chen, Xiaoyun; Song, Xiaoxiao
Organocatalytic asymmetric [4+2] cyclization of 2-benzothiazolimines with azlactones: access to chiral benzothiazolopyrimidine derivatives.
Chemical communications (Cambridge, England), 2020, 56, 3155-3158
7125982 CIFC21 H23 Cl F3 N5 OP 1 21/n 111.0699; 23.359; 16.6594
90; 96.992; 90		4275.8Carreira-Barral, Israel; Mielczarek, Marcin; Alonso-Carrillo, Daniel; Capurro, Valeria; Soto-Cerrato, Vanessa; Pérez Tomás, Ricardo; Caci, Emanuela; García-Valverde, María; Quesada, Roberto
Click-tambjamines as efficient and tunable bioactive anion transporters.
Chemical communications (Cambridge, England), 2020, 56, 3218-3221
7125983 CIFC24 H35 Cl2 N5 O3P -17.9219; 9.5881; 19.0533
99.49; 91.0584; 110.626		1331.31Carreira-Barral, Israel; Mielczarek, Marcin; Alonso-Carrillo, Daniel; Capurro, Valeria; Soto-Cerrato, Vanessa; Pérez Tomás, Ricardo; Caci, Emanuela; García-Valverde, María; Quesada, Roberto
Click-tambjamines as efficient and tunable bioactive anion transporters.
Chemical communications (Cambridge, England), 2020, 56, 3218-3221
7125984 CIFC17 H17 Cl2 N5 OP 1 21/c 15.7035; 20.182; 15.891
90; 96.478; 90		1817.5Carreira-Barral, Israel; Mielczarek, Marcin; Alonso-Carrillo, Daniel; Capurro, Valeria; Soto-Cerrato, Vanessa; Pérez Tomás, Ricardo; Caci, Emanuela; García-Valverde, María; Quesada, Roberto
Click-tambjamines as efficient and tunable bioactive anion transporters.
Chemical communications (Cambridge, England), 2020, 56, 3218-3221
7125985 CIFC14 H19 N0 O2P b c a9.026; 11.173; 23.919
90; 90; 90		2412.2Zhai, Shengxian; Qiu, Shuxian; Chen, Lunjian; Niu, Yongsheng; Yu, Youzhu; Yang, Bo; Zhang, Beining; Han, Chuchu; Yang, Liguo; Zhai, Hongbin
Synthesis of cyclobutane-fused oxygen-containing tricyclic framework via thermally promoted intramolecular cycloaddition of cyclohexadienone-tethered allenes.
Chemical communications (Cambridge, England), 2020, 56, 3405-3408
7125986 CIFC27 H29 N3 SeP 1 21/c 115.3492; 13.4033; 11.3497
90; 92.454; 90		2332.8Zhu, Li-Li; Tian, Lifang; Cai, Bin; Liu, Guanglu; Zhang, Hui; Wang, Yahui
Diamine-mediated N<sup>2</sup>-selective β-selenoalkylation of triazoles with alkenes.
Chemical communications (Cambridge, England), 2020, 56, 2979-2982
7125987 CIFC20 H23 N3 SeP 1 21 111.6605; 5.8592; 13.2196
90; 92.925; 90		902Zhu, Li-Li; Tian, Lifang; Cai, Bin; Liu, Guanglu; Zhang, Hui; Wang, Yahui
Diamine-mediated N<sup>2</sup>-selective β-selenoalkylation of triazoles with alkenes.
Chemical communications (Cambridge, England), 2020, 56, 2979-2982
7125988 CIFC29 H42 F6 N4 O6 S2P b c a14.61721; 17.96113; 27.42571
90; 90; 90		7200.39Barthes, Cécile; Duhayon, Carine; Canac, Yves; César, Vincent
N-Cyclopropenio-imidazol-2-ylidene: An N-heterocyclic carbene bearing an N-cationic substituent.
Chemical communications (Cambridge, England), 2020, 56, 3305-3308
7125989 CIFC31.5 H47 Cl2 F3 N4 O3 Pd SP -18.9948; 12.5902; 17.7787
78.6427; 82.2769; 88.4754		1956.04Barthes, Cécile; Duhayon, Carine; Canac, Yves; César, Vincent
N-Cyclopropenio-imidazol-2-ylidene: An N-heterocyclic carbene bearing an N-cationic substituent.
Chemical communications (Cambridge, England), 2020, 56, 3305-3308
7125990 CIFC28 H41 Au Cl F3 N4 O3 SP 1 21/n 115.1363; 8.9448; 26.1314
90; 103.763; 90		3436.4Barthes, Cécile; Duhayon, Carine; Canac, Yves; César, Vincent
N-Cyclopropenio-imidazol-2-ylidene: An N-heterocyclic carbene bearing an N-cationic substituent.
Chemical communications (Cambridge, England), 2020, 56, 3305-3308
7125991 CIFC30 H28 Cl2 N6 Ni O8 S2C 1 c 121.948; 8.33062; 20.7006
90; 115.404; 90		3418.9Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125992 CIFC24 H16 Cl2 N4 Ni S2P -18.9125; 12.1348; 12.2295
67.774; 69.928; 87.213		1144.97Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125993 CIFC29 H22 F6 N4 Ni O S2P -110.3997; 12.7078; 13.3086
114.49; 111.726; 92.4482		1446.31Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125994 CIFC26 H24 Cl2 N4 Ni O8 S2P 21 21 218.5516; 10.2011; 33.0145
90; 90; 90		2880.04Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125995 CIFC27 H25 N5 Ni O S2P 1 21/c 111.3962; 18.9231; 12.9723
90; 114.313; 90		2549.38Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125996 CIFC46 H50 Cl6 Co N4 Ni S2P -110.1761; 12.4123; 19.1814
96.674; 91.868; 96.713		2387.24Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125997 CIFC46 H52 Cl4 Co N4 Ni S2P 1 21/n 112.3345; 22.2711; 18.1248
90; 109.54; 90		4692.2Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125998 CIFC17 H16 Br N O2P 1 21/c 115.7754; 8.5582; 11.6197
90; 107.162; 90		1498.91Li, Xingjun; Wang, Jiang; Xie, Xiong; Dai, Wenhao; Han, Xu; Chen, Kaixian; Liu, Hong
Ir(iii)-Catalyzed direct C-H functionalization of N-phenylacetamide with α-diazo quinones: a novel strategy for producing 2-hydroxy-2'-amino-1,2'-biaryl scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 3441-3444
7125999 CIFC20 H14 Br N O3P 21 21 214.2743; 15.4368; 24.939
90; 90; 90		1645.5Li, Xingjun; Wang, Jiang; Xie, Xiong; Dai, Wenhao; Han, Xu; Chen, Kaixian; Liu, Hong
Ir(iii)-Catalyzed direct C-H functionalization of N-phenylacetamide with α-diazo quinones: a novel strategy for producing 2-hydroxy-2'-amino-1,2'-biaryl scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 3441-3444
7126000 CIFC18 H18 Br N O2P c a 2111.5591; 7.965; 17.2106
90; 90; 90		1584.55Li, Xingjun; Wang, Jiang; Xie, Xiong; Dai, Wenhao; Han, Xu; Chen, Kaixian; Liu, Hong
Ir(iii)-Catalyzed direct C-H functionalization of N-phenylacetamide with α-diazo quinones: a novel strategy for producing 2-hydroxy-2'-amino-1,2'-biaryl scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 3441-3444
7126001 CIFC18 H14 Br N O2P b c a8.3242; 12.6129; 28.2407
90; 90; 90		2965.06Li, Xingjun; Wang, Jiang; Xie, Xiong; Dai, Wenhao; Han, Xu; Chen, Kaixian; Liu, Hong
Ir(iii)-Catalyzed direct C-H functionalization of N-phenylacetamide with α-diazo quinones: a novel strategy for producing 2-hydroxy-2'-amino-1,2'-biaryl scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 3441-3444
7126002 CIFC18 H18 F3 N O2P 1 21 111.25978; 5.81649; 12.31963
90; 94.0216; 90		804.855Sun, Xi-Shang; Ou-Yang, Qiu; Xu, Shi-Ming; Wang, Xing-Heng; Tao, Hai-Yan; Chung, Lung Wa; Wang, Chun-Jiang
Asymmetric synthesis of quaternary α-trifluoromethyl α-amino acids by Ir-catalyzed allylation followed by kinetic resolution.
Chemical communications (Cambridge, England), 2020, 56, 3333-3336
7126003 CIFC18 H18 F3 N O2P 21 21 215.7902; 8.6739; 32.4787
90; 90; 90		1631.2Sun, Xi-Shang; Ou-Yang, Qiu; Xu, Shi-Ming; Wang, Xing-Heng; Tao, Hai-Yan; Chung, Lung Wa; Wang, Chun-Jiang
Asymmetric synthesis of quaternary α-trifluoromethyl α-amino acids by Ir-catalyzed allylation followed by kinetic resolution.
Chemical communications (Cambridge, England), 2020, 56, 3333-3336
7126004 CIFC22 H19 Cl N2 O2 SP 1 21/c 16.7878; 22.1588; 13.8692
90; 96.581; 90		2072.31Zhang, Jun; Yang, Min; Liu, Jin-Biao; He, Fu-Sheng; Wu, Jie
A copper-catalyzed insertion of sulfur dioxide via radical coupling.
Chemical communications (Cambridge, England), 2020, 56, 3225-3228
7126005 CIFC14 H17 N3 O5P 1 21/c 17.1763; 28.9373; 7.067
90; 92.186; 90		1466.48Fellowes, Thomas; Harris, Benjamin L.; White, Jonathan M.
Experimental evidence of chalcogen bonding at oxygen.
Chemical communications (Cambridge, England), 2020, 56, 3313-3316
7126006 CIFC9 H9 N3 O5P 21 21 215.4911; 10.5173; 18.2619
90; 90; 90		1054.65Fellowes, Thomas; Harris, Benjamin L.; White, Jonathan M.
Experimental evidence of chalcogen bonding at oxygen.
Chemical communications (Cambridge, England), 2020, 56, 3313-3316
7126007 CIFC12 H13 N3 O5P 1 21 16.6674; 16.3925; 11.6108
90; 101.031; 90		1245.56Fellowes, Thomas; Harris, Benjamin L.; White, Jonathan M.
Experimental evidence of chalcogen bonding at oxygen.
Chemical communications (Cambridge, England), 2020, 56, 3313-3316
7126008 CIFC33 H16 B F9 O2P -19.717; 10.2493; 15.4586
85.283; 75.672; 66.463		1367.33Gazis, Theodore A.; Mohajeri Thaker, Bayan A. J.; Willcox, Darren; Ould, Darren M. C.; Wenz, Jan; Rawson, Jeremy M.; Hill, Michael S.; Wirth, Thomas; Melen, Rebecca L.
1,3-Carboboration of iodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 3345-3348
7126009 CIFC23 H12 B F9 O4P -17.8452; 10.557; 15.699
71.33; 75.721; 84.401		1193.5Gazis, Theodore A.; Mohajeri Thaker, Bayan A. J.; Willcox, Darren; Ould, Darren M. C.; Wenz, Jan; Rawson, Jeremy M.; Hill, Michael S.; Wirth, Thomas; Melen, Rebecca L.
1,3-Carboboration of iodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 3345-3348
7126010 CIFC23 H6 B F15 O4P 1 21/n 113.314; 10.1081; 18.044
90; 111.202; 90		2264Gazis, Theodore A.; Mohajeri Thaker, Bayan A. J.; Willcox, Darren; Ould, Darren M. C.; Wenz, Jan; Rawson, Jeremy M.; Hill, Michael S.; Wirth, Thomas; Melen, Rebecca L.
1,3-Carboboration of iodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 3345-3348
7126011 CIFC24 H14 B F9 O3P 1 21/c 19.0378; 17.4814; 14.4485
90; 96.721; 90		2267.1Gazis, Theodore A.; Mohajeri Thaker, Bayan A. J.; Willcox, Darren; Ould, Darren M. C.; Wenz, Jan; Rawson, Jeremy M.; Hill, Michael S.; Wirth, Thomas; Melen, Rebecca L.
1,3-Carboboration of iodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 3345-3348
7126012 CIFC32 H15 B F15 I O2P 1 21/n 116.1557; 37.6672; 16.7091
90; 104.564; 90		9841.4Gazis, Theodore A.; Mohajeri Thaker, Bayan A. J.; Willcox, Darren; Ould, Darren M. C.; Wenz, Jan; Rawson, Jeremy M.; Hill, Michael S.; Wirth, Thomas; Melen, Rebecca L.
1,3-Carboboration of iodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 3345-3348
7126013 CIFC34 H36 N4 O8C 1 2/c 118.896; 15.0948; 22.5368
90; 103.389; 90		6253.5Johnson, Stuart; Kovács, Ervin; Greaney, Michael F.
Arylation and alkenylation of activated alkyl halides using sulfonamides.
Chemical communications (Cambridge, England), 2020, 56, 3222-3224
7126014 CIFC22 H29 N3P 1 21/n 116.2354; 5.8866; 20.5287
90; 93.513; 90		1958.3Sarkar, Tanumay; Talukdar, Kangkan; Roy, Subhasish; Punniyamurthy, Tharmalingam
Expedient iron-catalyzed stereospecific synthesis of triazines via cycloaddition of aziridines with diaziridines.
Chemical communications (Cambridge, England), 2020, 56, 3381-3384
7126015 CIFC28 H33 N3 O2P -16.1688; 10.0037; 20.56
103.548; 91.18; 95.599		1226.3Sarkar, Tanumay; Talukdar, Kangkan; Roy, Subhasish; Punniyamurthy, Tharmalingam
Expedient iron-catalyzed stereospecific synthesis of triazines via cycloaddition of aziridines with diaziridines.
Chemical communications (Cambridge, England), 2020, 56, 3381-3384
7126016 CIFC18 H16 N5 O2C 1 2/c 128.46; 4.932; 24.318
90; 112.81; 90		3146.4Borilovic, Ivana; Alonso, Pablo J.; Roubeau, Olivier; Aromí, Guillem
A bis-vanadyl coordination complex as a 2-qubit quantum gate.
Chemical communications (Cambridge, England), 2020, 56, 3139-3142
7126017 CIFC68 H94 N10 O6 Ti2P 1 21/n 112.3192; 17.5994; 14.9947
90; 96.71; 90		3228.7Borilovic, Ivana; Alonso, Pablo J.; Roubeau, Olivier; Aromí, Guillem
A bis-vanadyl coordination complex as a 2-qubit quantum gate.
Chemical communications (Cambridge, England), 2020, 56, 3139-3142
7126018 CIFC68 H94 N10 O6 Ti2P -19.9438; 12.8964; 13.5489
86.435; 79.518; 74.129		1643.23Borilovic, Ivana; Alonso, Pablo J.; Roubeau, Olivier; Aromí, Guillem
A bis-vanadyl coordination complex as a 2-qubit quantum gate.
Chemical communications (Cambridge, England), 2020, 56, 3139-3142
7126019 CIFC88 H114 N14 O6 Ti2P -112.7936; 18.121; 19.6033
98.602; 108.452; 101.429		4113.9Borilovic, Ivana; Alonso, Pablo J.; Roubeau, Olivier; Aromí, Guillem
A bis-vanadyl coordination complex as a 2-qubit quantum gate.
Chemical communications (Cambridge, England), 2020, 56, 3139-3142
7126020 CIFC90.5 H116.5 N14.5 O6 V2P -112.807; 18.384; 20.411
73.022; 72.779; 70.673		4230Borilovic, Ivana; Alonso, Pablo J.; Roubeau, Olivier; Aromí, Guillem
A bis-vanadyl coordination complex as a 2-qubit quantum gate.
Chemical communications (Cambridge, England), 2020, 56, 3139-3142
7126021 CIFC12 H48 In6 N6 S12P 1 21/n 19.742; 14.4225; 28.1311
90; 93.409; 90		3945.54Wang, Kai-Yao; Sun, Meng; Ding, Dong; Liu, Hua-Wei; Cheng, Lin; Wang, Cheng
Di-lacunary [In<sub>6</sub>S<sub>15</sub>]<sup>12-</sup> cluster: the building block of a highly negatively charged framework for superior Sr<sup>2+</sup> adsorption capacities.
Chemical communications (Cambridge, England), 2020, 56, 3409-3412
7126022 CIFC2 H5 Na OP -4 21 m4.41084; 4.41084; 9.06779
90; 90; 90		176.418Beske, Maurice; Tapmeyer, Lukas; Schmidt, Martin U.
Crystal structure of sodium ethoxide (C<sub>2</sub>H<sub>5</sub>ONa), unravelled after 180 years.
Chemical communications (Cambridge, England), 2020, 56, 3520-3523
7126023 CIFC6 H17 Na O3P 1 21/n 111.622; 5.1926; 17.682
90; 104.08; 90		1035Beske, Maurice; Tapmeyer, Lukas; Schmidt, Martin U.
Crystal structure of sodium ethoxide (C<sub>2</sub>H<sub>5</sub>ONa), unravelled after 180 years.
Chemical communications (Cambridge, England), 2020, 56, 3520-3523
7126024 CIFC10 H17 Au Cl3 N3 OP 1 21/c 17.0041; 15.654; 16.326
90; 115.405; 90		1616.9Terrón, Angel; Buils, Jordi; Mooibroek, Tiddo J.; Barceló-Oliver, Miquel; García-Raso, Angel; Fiol, Juan J.; Frontera, Antonio
Synthesis, X-ray characterization and regium bonding interactions of a trichlorido(1-hexylcytosine)gold(iii) complex.
Chemical communications (Cambridge, England), 2020, 56, 3524-3527
7126025 CIFC42 H40 Cu2 N8C 1 2/c 125.3657; 9.9388; 29.1779
90; 92.788; 90		7347.2Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126026 CIFC42 H40 Cu2 N8 Ne3.5C 1 2/c 124.115; 9.2099; 26.461
90; 83.888; 90		5843.5Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126027 CIFC42 H40 Cu2 N8C 1 2/c 124.808; 9.6971; 27.648
90; 92.073; 90		6646.8Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126028 CIFC42 H40 Cu2 N8 Ne3.5C 1 2/c 124.215; 9.2391; 26.599
90; 84.042; 90		5919Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126029 CIFC42 H40 Cu2 N8C 1 2/c 125.1863; 9.9249; 28.57
90; 91.745; 90		7138.4Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126030 CIFC42 H40 Cu2 N8 Ne3.5C 1 2/c 124.259; 9.2882; 26.841
90; 84.039; 90		6015Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126031 CIFC42 H40 Cu2 N8 Ne3.5C 1 2/c 123.997; 9.1398; 26.116
90; 83.75; 90		5693.9Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126032 CIFC42 H40 Cu2 N8 Ne3.5C 1 2/c 123.811; 9.0709; 25.766
90; 83.532; 90		5530Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126033 CIFC42 H40 Cu2 N8C 1 2/c 124.281; 9.4519; 26.2355
90; 91.553; 90		6018.9Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126034 CIFC18 H26 Eu F4 N5 O9 S4P 4/n :212.782; 12.782; 8.4363
90; 90; 90		1378.32Zeng, Qi; Wang, Lei; Huang, Yitao; Zheng, Sai-Li; He, Yonghe; He, Jun; Liao, Wei-Ming; Xu, Gang; Zeller, Matthias; Xu, Zhengtao
An air-stable anionic two-dimensional semiconducting metal-thiolate network and its exfoliation into ultrathin few-layer nanosheets.
Chemical communications (Cambridge, England), 2020, 56, 3645-3648
7126035 CIFC12 H36 Ag Bi I12 N4P -18.6582; 9.3734; 12.1489
90.286; 95.226; 90.478		981.82Yao, Yunpeng; Kou, Bo; Peng, Yu; Wu, Zhenyue; Li, Lina; Wang, Sasa; Zhang, Xinyuan; Liu, Xitao; Luo, Junhua
(C<sub>3</sub>H<sub>9</sub>NI)<sub>4</sub>AgBiI<sub>8</sub>: a direct-bandgap layered double perovskite based on a short-chain spacer cation for light absorption.
Chemical communications (Cambridge, England), 2020, 56, 3206-3209
7126036 CIFC52 H38 F5 N3P -112.1765; 13.0482; 15.231
111.513; 112.548; 93.946		2016.53Das, Mainak; Chitranshi, Sangya; Murugavel, M.; Adinarayana, B.; Suresh, Cherumuttathu H.; Srinivasan, A.
Isosmaragdyrin with an N<sub>3</sub>C<sub>2</sub> core: stabilization of Rh(i) and organo-Pt(ii) complexes.
Chemical communications (Cambridge, England), 2020, 56, 3551-3554
7126037 CIFC400 H344 Cl F72 N80 Pt8C 1 2/c 131.6392; 8.7956; 37.084
90; 93.548; 90		10300.2Das, Mainak; Chitranshi, Sangya; Murugavel, M.; Adinarayana, B.; Suresh, Cherumuttathu H.; Srinivasan, A.
Isosmaragdyrin with an N<sub>3</sub>C<sub>2</sub> core: stabilization of Rh(i) and organo-Pt(ii) complexes.
Chemical communications (Cambridge, England), 2020, 56, 3551-3554
7126038 CIFC54 H39 F5 N3 O2 RhC 2 2 2112.7471; 24.2024; 35.7587
90; 90; 90		11031.9Das, Mainak; Chitranshi, Sangya; Murugavel, M.; Adinarayana, B.; Suresh, Cherumuttathu H.; Srinivasan, A.
Isosmaragdyrin with an N<sub>3</sub>C<sub>2</sub> core: stabilization of Rh(i) and organo-Pt(ii) complexes.
Chemical communications (Cambridge, England), 2020, 56, 3551-3554
7126039 CIFC36 H21 N5 O2 SI 1 2/a 117.1162; 7.7907; 42.35
90; 90.551; 90		5647Bui, Anh Thy; Philippe, Clotilde; Beau, Maxime; Richy, Nicolas; Cordier, Marie; Roisnel, Thierry; Lemiègre, Loïc; Mongin, Olivier; Paul, Frédéric; Trolez, Yann
Synthesis, characterization and unusual near-infrared luminescence of 1,1,4,4-tetracyanobutadiene derivatives.
Chemical communications (Cambridge, England), 2020, 56, 3571-3574
7126040 CIFC32 H19 N5 O2 SP 1 21/n 18.766; 26.272; 11.5682
90; 109.987; 90		2503.7Bui, Anh Thy; Philippe, Clotilde; Beau, Maxime; Richy, Nicolas; Cordier, Marie; Roisnel, Thierry; Lemiègre, Loïc; Mongin, Olivier; Paul, Frédéric; Trolez, Yann
Synthesis, characterization and unusual near-infrared luminescence of 1,1,4,4-tetracyanobutadiene derivatives.
Chemical communications (Cambridge, England), 2020, 56, 3571-3574
7126045 CIFC54 H72 As N3P 1 21/n 112.59029; 15.93625; 23.78509
90; 93.231; 90		4764.7Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126046 CIFC54 H72 As Cl4 Ga N3P -111.4502; 19.3524; 25.1018
76.229; 89.254; 88.856		5401.1Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126047 CIFC57 H76 As N3P 1 21/c 118.8381; 11.9051; 22.8999
90; 101.668; 90		5029.6Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126048 CIFC57 H76 As Cl8 Ga2 N3P -113.7117; 24.2939; 24.861
100.452; 98.045; 98.408		7937.7Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126049 CIFC57 H76 As Cl4 Ga N3P 1 21/n 112.6066; 23.8366; 18.7085
90; 98.41; 90		5561.4Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126050 CIFC54 H72 As Cl8 Ga2 N3P b c a18.8893; 26.1136; 24.2536
90; 90; 90		11963.5Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126051 CIFBa3 Cl3 F6 InP 63/m10.131; 10.131; 5.9315
90; 90; 120		527.23Jiang, Xiaoqing; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng
In[Ba<sub>3</sub>Cl<sub>3</sub>F<sub>6</sub>]: a novel infrared-transparent molecular sieve constructed by halides.
Chemical communications (Cambridge, England), 2020, 56, 3297-3300
7126052 CIFC16 H15 N3 O3P 1 21/c 17.053; 18.102; 11.924
90; 106.894; 90		1456.7Pal, Pranesh; Mainkar, Prathama S.; Nayani, Kiranmai; Chandrasekhar, Srivari
Mn-catalyzed radical initiated domino transformation of alkynylated cyclohexadienones with TMSN<sub>3</sub> and O<sub>2</sub> to bicyclic azido alcohols.
Chemical communications (Cambridge, England), 2020, 56, 3453-3456
7126053 CIFC90 H100 Ag12 F36 N12 O26 S6P b c a20.9281; 22.1548; 28.9986
90; 90; 90		13445.4Chen, Xu-Ran; Yang, Ling; Tan, Yu-Ling; Yu, Hong; Ni, Chun-Yan; Niu, Zheng; Lang, Jian-Ping
The solvent-induced isomerization of silver thiolate clusters with symmetry transformation.
Chemical communications (Cambridge, England), 2020, 56, 3649-3652
7126054 CIFC84 H92 Ag12 F36 N8 O26 S6C 1 2/c 130.2957; 20.8495; 22.4448
90; 114.615; 90		12888.9Chen, Xu-Ran; Yang, Ling; Tan, Yu-Ling; Yu, Hong; Ni, Chun-Yan; Niu, Zheng; Lang, Jian-Ping
The solvent-induced isomerization of silver thiolate clusters with symmetry transformation.
Chemical communications (Cambridge, England), 2020, 56, 3649-3652
7126055 CIFC82 H84 Ag12 F36 N8 O24 S6P 1 21/c 113.8315; 29.7018; 16.2995
90; 94.93; 90		6671.4Chen, Xu-Ran; Yang, Ling; Tan, Yu-Ling; Yu, Hong; Ni, Chun-Yan; Niu, Zheng; Lang, Jian-Ping
The solvent-induced isomerization of silver thiolate clusters with symmetry transformation.
Chemical communications (Cambridge, England), 2020, 56, 3649-3652
7126056 CIFC41 H54 Ag F6 N4 PI 49.6472; 9.6472; 21.411
90; 90; 90		1992.7Lee, Eunji; Hosoi, Yasuhiro; Temma, Honoka; Ju, Huiyeong; Ikeda, Mari; Kuwahara, Shunsuke; Habata, Yoichi
Silver ion-induced chiral enhancement by argentivorous molecules.
Chemical communications (Cambridge, England), 2020, 56, 3373-3376
7126057 CIFC37 H46 Ag B F4 N4C 1 2 113.8399; 13.5554; 18.233
90; 100.627; 90		3361.9Lee, Eunji; Hosoi, Yasuhiro; Temma, Honoka; Ju, Huiyeong; Ikeda, Mari; Kuwahara, Shunsuke; Habata, Yoichi
Silver ion-induced chiral enhancement by argentivorous molecules.
Chemical communications (Cambridge, England), 2020, 56, 3373-3376
7126058 CIFC41 H54 Ag F6 N4 PI 49.614; 9.614; 21.337
90; 90; 90		1972.2Lee, Eunji; Hosoi, Yasuhiro; Temma, Honoka; Ju, Huiyeong; Ikeda, Mari; Kuwahara, Shunsuke; Habata, Yoichi
Silver ion-induced chiral enhancement by argentivorous molecules.
Chemical communications (Cambridge, England), 2020, 56, 3373-3376
7126059 CIFC43 H62 N6 O8 ZnP 1 21 18.7797; 19.0092; 12.9597
90; 90.5449; 90		2162.8Lee, Eunji; Hosoi, Yasuhiro; Temma, Honoka; Ju, Huiyeong; Ikeda, Mari; Kuwahara, Shunsuke; Habata, Yoichi
Silver ion-induced chiral enhancement by argentivorous molecules.
Chemical communications (Cambridge, England), 2020, 56, 3373-3376
7126060 CIFC37 H42 Ag F10 N4 PC 2 2 2113.8896; 14.0055; 37.666
90; 90; 90		7327.2Lee, Eunji; Hosoi, Yasuhiro; Temma, Honoka; Ju, Huiyeong; Ikeda, Mari; Kuwahara, Shunsuke; Habata, Yoichi
Silver ion-induced chiral enhancement by argentivorous molecules.
Chemical communications (Cambridge, England), 2020, 56, 3373-3376
7126061 CIFC16 H12 B NP 1 21/c 19.493; 8.9361; 13.533
90; 96.47; 90		1140.7Abengózar, Alberto; Valencia, Isabel; Otárola, Guillermo G; Sucunza, David; García-García, Patricia; Pérez-Redondo, Adrián; Mendicuti, Francisco; Vaquero, Juan J.
Expanding the BN-embedded PAH family: 4a-aza-12a-borachrysene.
Chemical communications (Cambridge, England), 2020, 56, 3669-3672
7126062 CIFC154 H122 Cl6 O16P -111.895; 13.566; 21.429
89.762; 74.368; 73.348		3180Shimoyama, Daisuke; Sekiya, Ryo; Haino, Takeharu
Upper-rim functionalization and supramolecular polymerization of a feet-to-feet-connected biscavitand.
Chemical communications (Cambridge, England), 2020, 56, 3733-3736
7126063 CIFC50 H128 N25 Nd O88 Si2 W22P -113.4923; 19.9659; 24.448
102.869; 97.74; 94.707		6319.1Nie, Yan-Mei; Li, Sang-Hao; Lin, Ming-Yuan; Yan, Jun
A micro-environment tuning approach for enhancing the catalytic capabilities of lanthanide containing polyoxometalate in the cyanosilylation of ketones.
Chemical communications (Cambridge, England), 2020, 56, 3809-3812
7126064 CIFC94 H46 Ag13 F36 N12P -115.3728; 15.4794; 15.4872
61.894; 68.689; 61.905		2819.87Peng, Su-Kao; Lu, Zhou; Xie, Mo; Huang, Yong-Liang; Luo, Dong; Wang, Jia-Nan; Zhu, Xiao-Wei; Li, Xue; Zhou, Xiao-Ping; Li, Dan
Unexpected structural transformation into noria-like Ag<sub>13</sub> metal clusters and a copper-doping induced boost in photoluminescence.
Chemical communications (Cambridge, England), 2020, 56, 4789-4792
7126065 CIFC94 H46 Ag11.5 Cu1.5 F36 N12P -115.4952; 15.5896; 15.5997
61.283; 67.64; 61.42		2846.14Peng, Su-Kao; Lu, Zhou; Xie, Mo; Huang, Yong-Liang; Luo, Dong; Wang, Jia-Nan; Zhu, Xiao-Wei; Li, Xue; Zhou, Xiao-Ping; Li, Dan
Unexpected structural transformation into noria-like Ag<sub>13</sub> metal clusters and a copper-doping induced boost in photoluminescence.
Chemical communications (Cambridge, England), 2020, 56, 4789-4792
7126066 CIFC94 H46 Ag11.96 Cu F36 N12P -115.5019; 15.7093; 15.9495
60.608; 65.701; 61.289		2888.52Peng, Su-Kao; Lu, Zhou; Xie, Mo; Huang, Yong-Liang; Luo, Dong; Wang, Jia-Nan; Zhu, Xiao-Wei; Li, Xue; Zhou, Xiao-Ping; Li, Dan
Unexpected structural transformation into noria-like Ag<sub>13</sub> metal clusters and a copper-doping induced boost in photoluminescence.
Chemical communications (Cambridge, England), 2020, 56, 4789-4792
7126067 CIFC14 H10 Cl N SP 1 21/n 17.994; 5.8548; 25.946
90; 92.333; 90		1213.4Reddy, Mandapati Bhargava; Anandhan, Ramasamy
Visible light initiated amino group ortho-directed copper(i)-catalysed aerobic oxidative C(sp)-S coupling reaction: synthesis of substituted 2-phenylbenzothiazoles via thia-Wolff rearrangement.
Chemical communications (Cambridge, England), 2020, 56, 3781-3784
7126068 CIFC37 H36 F3 N O6P 1 21/n 16.4039; 49.826; 9.4014
90; 90.163; 90		2999.8Matsuhashi, Chihiro; Ueno, Takuya; Uekusa, Hidehiro; Sato-Tomita, Ayana; Ichiyanagi, Kouhei; Maki, Shojiro; Hirano, Takashi
Isomeric difference in the crystalline-state chemiluminescence property of an adamantylideneadamantane 1,2-dioxetane with a phthalimide chromophore.
Chemical communications (Cambridge, England), 2020, 56, 3369-3372
7126069 CIFC37 H36 F3 N O6P -16.847; 9.989; 23.661
81.861; 81.721; 71.02		1506.6Matsuhashi, Chihiro; Ueno, Takuya; Uekusa, Hidehiro; Sato-Tomita, Ayana; Ichiyanagi, Kouhei; Maki, Shojiro; Hirano, Takashi
Isomeric difference in the crystalline-state chemiluminescence property of an adamantylideneadamantane 1,2-dioxetane with a phthalimide chromophore.
Chemical communications (Cambridge, England), 2020, 56, 3369-3372
7126070 CIFC47 H40 Cl2 Co2 N10 O16C 1 2/c 116.718; 13.417; 22.998
90; 101.935; 90		5047.1Chai, Xiaomin; Huang, Hai-Hua; Liu, Huiping; Ke, Zhuofeng; Yong, Wen-Wen; Zhang, Ming-Tian; Cheng, Yuan-Sheng; Wei, Xian-Wen; Zhang, Liyan; Yuan, Guozan
Highly efficient and selective photocatalytic CO<sub>2</sub> to CO conversion in aqueous solution.
Chemical communications (Cambridge, England), 2020, 56, 3851-3854
7126071 CIFC46 H40 Cl2 Fe2 N10 O12C 1 2/c 115.885; 13.472; 23.262
90; 100.741; 90		4891Chai, Xiaomin; Huang, Hai-Hua; Liu, Huiping; Ke, Zhuofeng; Yong, Wen-Wen; Zhang, Ming-Tian; Cheng, Yuan-Sheng; Wei, Xian-Wen; Zhang, Liyan; Yuan, Guozan
Highly efficient and selective photocatalytic CO<sub>2</sub> to CO conversion in aqueous solution.
Chemical communications (Cambridge, England), 2020, 56, 3851-3854
7126072 CIFC24 H23 Cl Mn N5 O6P 21 21 219.033; 11.082; 24.474
90; 90; 90		2449.9Chai, Xiaomin; Huang, Hai-Hua; Liu, Huiping; Ke, Zhuofeng; Yong, Wen-Wen; Zhang, Ming-Tian; Cheng, Yuan-Sheng; Wei, Xian-Wen; Zhang, Liyan; Yuan, Guozan
Highly efficient and selective photocatalytic CO<sub>2</sub> to CO conversion in aqueous solution.
Chemical communications (Cambridge, England), 2020, 56, 3851-3854
7126073 CIFC24 H20 Cl Cu N5 O6P -113.82; 14.61; 14.99
62.12; 76.15; 71.48		2522Chai, Xiaomin; Huang, Hai-Hua; Liu, Huiping; Ke, Zhuofeng; Yong, Wen-Wen; Zhang, Ming-Tian; Cheng, Yuan-Sheng; Wei, Xian-Wen; Zhang, Liyan; Yuan, Guozan
Highly efficient and selective photocatalytic CO<sub>2</sub> to CO conversion in aqueous solution.
Chemical communications (Cambridge, England), 2020, 56, 3851-3854
7126074 CIFC23 H20 Cl N5 Ni O6P 1 21/n 112.15; 13.633; 14.455
90; 107.636; 90		2282Chai, Xiaomin; Huang, Hai-Hua; Liu, Huiping; Ke, Zhuofeng; Yong, Wen-Wen; Zhang, Ming-Tian; Cheng, Yuan-Sheng; Wei, Xian-Wen; Zhang, Liyan; Yuan, Guozan
Highly efficient and selective photocatalytic CO<sub>2</sub> to CO conversion in aqueous solution.
Chemical communications (Cambridge, England), 2020, 56, 3851-3854
7126075 CIFC84 H138 Cl16 Dy6 K4 O6P -113.9788; 16.4794; 37.2813
85.933; 84.334; 70.868		8067.4Wu, Jianfeng; Demeshko, Serhiy; Dechert, Sebastian; Meyer, Franc
Hexanuclear [Cp*Dy]<sub>6</sub> single-molecule magnet.
Chemical communications (Cambridge, England), 2020, 56, 3887-3890
7126076 CIFC112 H80 Cl2P 1 21/c 125.9806; 24.253; 26.5964
90; 97.253; 90		16624.5Yu, Jie; Tang, Chunlin; Gu, Xinggui; Zheng, Xiaoyan; Yu, Zhen-Qiang; He, Zikai; Li, Xin-Gui; Tang, Ben Zhong
Highly emissive phenylene-expanded [5]radialene.
Chemical communications (Cambridge, England), 2020, 56, 3911-3914
7126077 CIFC129 H56 N4 Ni Sc1.75 U0.88C 1 2/c 125.2486; 15.0232; 39.512
90; 95.365; 90		14921.8Li, Xiaomeng; Yao, Yang-Rong; Yang, Wei; Zhuang, Jiaxin; Echegoyen, Luis; Chen, Ning
Crystallographic and spectroscopic characterization of a mixed actinide-lanthanide carbide cluster stabilized inside an I<sub>h</sub>(7)-C<sub>80</sub> fullerene cage.
Chemical communications (Cambridge, England), 2020, 56, 3867-3870
7126078 CIFC11 H10 F3 N3 O2P -16.1114; 8.7281; 20.9657
80.025; 89.183; 88.02		1100.73Wagner, Shana; Sudhamalla, Babu; Mannes, Philip; Sappa, Sushma; Kavoosi, Sam; Dey, Debasis; Wang, Sinan; Islam, Kabirul
Engineering bromodomains with a photoactive amino acid by engaging 'Privileged' tRNA synthetases.
Chemical communications (Cambridge, England), 2020, 56, 3641-3644
7126079 CIFC23 H19 F3 N2 Ni O2 SP 1 21/n 16.9629; 27.163; 11.1046
90; 96.72; 90		2085.8Berkefeld, Andreas; Fröhlich, Markus; Kordan, Mike; Hörner, Gerald; Schubert, Hartmut
Selective metalation of phenol-type proligands for preparative organometallic chemistry.
Chemical communications (Cambridge, England), 2020, 56, 3987-3990
7126080 CIFC30 H30 F N2 Ni O2P 1 2/c 114.4635; 6.9797; 25.786
90; 100.159; 90		2562.3Berkefeld, Andreas; Fröhlich, Markus; Kordan, Mike; Hörner, Gerald; Schubert, Hartmut
Selective metalation of phenol-type proligands for preparative organometallic chemistry.
Chemical communications (Cambridge, England), 2020, 56, 3987-3990
7126081 CIFC28 H37 N3 Ni O Si2P 1 21/c 111.9534; 13.7247; 17.1253
90; 93.572; 90		2804.1Berkefeld, Andreas; Fröhlich, Markus; Kordan, Mike; Hörner, Gerald; Schubert, Hartmut
Selective metalation of phenol-type proligands for preparative organometallic chemistry.
Chemical communications (Cambridge, England), 2020, 56, 3987-3990
7126082 CIFC42 H55.5 N4.5 Ni1.5 Si3P 1 21/c 123.5957; 13.6797; 26.9113
90; 101.433; 90		8514.1Berkefeld, Andreas; Fröhlich, Markus; Kordan, Mike; Hörner, Gerald; Schubert, Hartmut
Selective metalation of phenol-type proligands for preparative organometallic chemistry.
Chemical communications (Cambridge, England), 2020, 56, 3987-3990
7126083 CIFC62 H70 F6 N4 Ni2 O11 S2P -112.8801; 14.0913; 17.4958
81.586; 77.019; 84.657		3055Berkefeld, Andreas; Fröhlich, Markus; Kordan, Mike; Hörner, Gerald; Schubert, Hartmut
Selective metalation of phenol-type proligands for preparative organometallic chemistry.
Chemical communications (Cambridge, England), 2020, 56, 3987-3990
7126084 CIFC55 H63 B N5 O2 Si2 YP 1 21/c 112.054; 22.253; 20.28
90; 93.554; 90		5429Ma, Yan; Zhai, Yuan-Qi; Ding, You-Song; Han, Tian; Zheng, Yan-Zhen
Understanding a pentagonal-bipyramidal holmium(iii) complex with a record energy barrier for magnetisation reversal.
Chemical communications (Cambridge, England), 2020, 56, 3979-3982
7126085 CIFC70 H68 B Ho N6 O2P 21 21 221.104; 25.522; 11.123
90; 90; 90		5991Ma, Yan; Zhai, Yuan-Qi; Ding, You-Song; Han, Tian; Zheng, Yan-Zhen
Understanding a pentagonal-bipyramidal holmium(iii) complex with a record energy barrier for magnetisation reversal.
Chemical communications (Cambridge, England), 2020, 56, 3979-3982
7126086 CIFC67 H75 B Ho N8 O2 Si2P -113.665; 14.335; 17.329
95.521; 108.465; 90.85		3201.2Ma, Yan; Zhai, Yuan-Qi; Ding, You-Song; Han, Tian; Zheng, Yan-Zhen
Understanding a pentagonal-bipyramidal holmium(iii) complex with a record energy barrier for magnetisation reversal.
Chemical communications (Cambridge, England), 2020, 56, 3979-3982
7126087 CIFC75 H73.5 B Ho N7 O2P -115.645; 15.651; 28.55
101.047; 93.207; 90.009		6850Ma, Yan; Zhai, Yuan-Qi; Ding, You-Song; Han, Tian; Zheng, Yan-Zhen
Understanding a pentagonal-bipyramidal holmium(iii) complex with a record energy barrier for magnetisation reversal.
Chemical communications (Cambridge, England), 2020, 56, 3979-3982
7126088 CIFC24 H14 Br N O2P -16.7672; 9.2017; 15.1089
81.431; 82.868; 80.818		913.54Liu, Jing; Ba, Dan; Chen, Yanhui; Wen, Si; Cheng, Guolin
Synthesis of 3-(2-quinolyl) chromones from ynones and quinoline N-oxides via tandem reactions under transition metal- and additive-free conditions.
Chemical communications (Cambridge, England), 2020, 56, 4078-4081
7126089 CIFC22 H16 N2 O2P 1 21/c 19.3098; 10.3197; 18.503
90; 91.529; 90		1777Zhang, Cong-Hai; Huang, Rong; Qing, Xia; Lin, Jun; Yan, Sheng-Jiao
Cascade reaction of isatins with nitro-substituted enamines: highly selective synthesis of functionalized (Z)-3-(1-(arylamino)-2-oxoarylidene)indolin-2-ones.
Chemical communications (Cambridge, England), 2020, 56, 3488-3491
7126090 CIFC72 H94 Mn2 N6P 1 21/n 112.3092; 12.735; 20.557
90; 92.955; 90		3218.2Nguyen, Thao T.; Kim, Jun-Hyeong; Kim, Suyeon; Oh, Changjin; Flores, Marco; Groy, Thomas L.; Baik, Mu-Hyun; Trovitch, Ryan J.
Scope and mechanism of nitrile dihydroboration mediated by a β-diketiminate manganese hydride catalyst.
Chemical communications (Cambridge, England), 2020, 56, 3959-3962
7126091 CIFC40 H30 N2P 1 21/n 113.1968; 17.0333; 19.6066
90; 101.946; 90		4311.82Zhang, Chi; Jiao, Tianyu; Tong, Lu; Wang, Hongye; Pan, Yuanjiang; Li, Hao
High yielding self-assembly favored by preorganization.
Chemical communications (Cambridge, England), 2020, 56, 3903-3906
7126092 CIFC62 H53 Cl6 N3P -113.119; 15.227; 15.449
106.247; 109.671; 101.252		2643.3Zhang, Chi; Jiao, Tianyu; Tong, Lu; Wang, Hongye; Pan, Yuanjiang; Li, Hao
High yielding self-assembly favored by preorganization.
Chemical communications (Cambridge, England), 2020, 56, 3903-3906
7126093 CIFC63 H54 Cl9 N3P -111.337; 20.266; 26.705
71.662; 84.799; 86.827		5798Zhang, Chi; Jiao, Tianyu; Tong, Lu; Wang, Hongye; Pan, Yuanjiang; Li, Hao
High yielding self-assembly favored by preorganization.
Chemical communications (Cambridge, England), 2020, 56, 3903-3906
7126094 CIFC26 H48 Co8 K N8 O12 S2R -3 :H13.4577; 13.4577; 20.3224
90; 90; 120		3187.48Yu, You-Zhu; Guo, Yu-Hua; Zhang, Yan-Ru; Tian, Xiu-Juan; Zhang, Xian-Ming
Tetrahedral μ<sub>4</sub>-chloride and in situ generated octahedral μ<sub>6</sub>-sulfide templating Co<sub>8</sub> complexes with different distortions of the cube.
Chemical communications (Cambridge, England), 2020, 56, 4236-4239
7126095 CIFC26 H51 Cl4 Co8 N5 O12R 3 m :H14.8782; 14.8782; 16.9496
90; 90; 120		3249.3Yu, You-Zhu; Guo, Yu-Hua; Zhang, Yan-Ru; Tian, Xiu-Juan; Zhang, Xian-Ming
Tetrahedral μ<sub>4</sub>-chloride and in situ generated octahedral μ<sub>6</sub>-sulfide templating Co<sub>8</sub> complexes with different distortions of the cube.
Chemical communications (Cambridge, England), 2020, 56, 4236-4239
7126096 CIFC58 H71 Ce F12 K N6 O8P 1 21/c 125.0707; 15.4308; 16.9537
90; 105.921; 90		6307.1Lapsheva, Ekaterina N.; Cheisson, Thibault; Álvarez Lamsfus, Carlos; Carroll, Patrick J.; Gau, Michael R.; Maron, Laurent; Schelter, Eric J.
Reactivity of Ce(iv) imido compounds with heteroallenes.
Chemical communications (Cambridge, England), 2020, 56, 4781-4784
7126097 CIFC109 H124.5 Ce2 Cs2 F12 N14.5 O10P -111.233; 14.495; 20.522
70.871; 75.802; 72.404		2969.3Lapsheva, Ekaterina N.; Cheisson, Thibault; Álvarez Lamsfus, Carlos; Carroll, Patrick J.; Gau, Michael R.; Maron, Laurent; Schelter, Eric J.
Reactivity of Ce(iv) imido compounds with heteroallenes.
Chemical communications (Cambridge, England), 2020, 56, 4781-4784
7126098 CIFC118 H160 Ce2 F12 N12 O10 Rb2P b c n32.651; 17.14; 23.603
90; 90; 90		13209Lapsheva, Ekaterina N.; Cheisson, Thibault; Álvarez Lamsfus, Carlos; Carroll, Patrick J.; Gau, Michael R.; Maron, Laurent; Schelter, Eric J.
Reactivity of Ce(iv) imido compounds with heteroallenes.
Chemical communications (Cambridge, England), 2020, 56, 4781-4784
7126099 CIFC35 H47 N2 O ReP 1 21/n 110.1864; 25.6639; 12.2342
90; 106.406; 90		3068.08Lohrey, Trevor D.; Fostvedt, Jade I.; Bergman, Robert G.; Arnold, John
Electron acceptors promote proton-hydride tautomerism in low valent rhenium β-diketiminates.
Chemical communications (Cambridge, England), 2020, 56, 3761-3764
7126100 CIFC34 H47 N4 ReP 1 21/n 113.0017; 17.4412; 13.855
90; 98.992; 90		3103.22Lohrey, Trevor D.; Fostvedt, Jade I.; Bergman, Robert G.; Arnold, John
Electron acceptors promote proton-hydride tautomerism in low valent rhenium β-diketiminates.
Chemical communications (Cambridge, England), 2020, 56, 3761-3764
7126101 CIFC43 H56 N3 ReP 1 21/m 19.4458; 19.0455; 10.9694
90; 106.664; 90		1890.52Lohrey, Trevor D.; Fostvedt, Jade I.; Bergman, Robert G.; Arnold, John
Electron acceptors promote proton-hydride tautomerism in low valent rhenium β-diketiminates.
Chemical communications (Cambridge, England), 2020, 56, 3761-3764
7126102 CIFC78 H76 Cu F6 N4 O6 S2P -110.1269; 13.1476; 29.1917
97.319; 96.976; 111.49		3527.03Kałuża, Adrianna M; Mukherjee, Soumya; Wang, Shi-Qiang; O'Hearn, Daniel J; Zaworotko, Michael J.
[Cu(4-phenylpyridine)<sub>4</sub>(trifluoromethanesulfonate)<sub>2</sub>], a Werner complex that exhibits high selectivity for o-xylene.
Chemical communications (Cambridge, England), 2020, 56, 1940-1943
7126103 CIFC78 H76 Cu F6 N4 O6 S2P -110.249; 13.097; 15.188
72.156; 73.95; 68.985		1779.4Kałuża, Adrianna M; Mukherjee, Soumya; Wang, Shi-Qiang; O'Hearn, Daniel J; Zaworotko, Michael J.
[Cu(4-phenylpyridine)<sub>4</sub>(trifluoromethanesulfonate)<sub>2</sub>], a Werner complex that exhibits high selectivity for o-xylene.
Chemical communications (Cambridge, England), 2020, 56, 1940-1943
7126104 CIFC46 H36 Cu F6 N4 O6 S2P 111.743; 13.021; 15.225
72.071; 85.436; 89.509		2207.6Kałuża, Adrianna M; Mukherjee, Soumya; Wang, Shi-Qiang; O'Hearn, Daniel J; Zaworotko, Michael J.
[Cu(4-phenylpyridine)<sub>4</sub>(trifluoromethanesulfonate)<sub>2</sub>], a Werner complex that exhibits high selectivity for o-xylene.
Chemical communications (Cambridge, England), 2020, 56, 1940-1943
7126105 CIFC78 H76 Cu F6 N4 O6 S2P -110.166; 13.051; 15.236
72.382; 74.26; 69.168		1770.1Kałuża, Adrianna M; Mukherjee, Soumya; Wang, Shi-Qiang; O'Hearn, Daniel J; Zaworotko, Michael J.
[Cu(4-phenylpyridine)<sub>4</sub>(trifluoromethanesulfonate)<sub>2</sub>], a Werner complex that exhibits high selectivity for o-xylene.
Chemical communications (Cambridge, England), 2020, 56, 1940-1943
7126106 CIFC78 H76 Cu F6 N4 O6 S2P -110.2443; 13.0741; 15.129
72.449; 73.851; 69.024		1770.7Kałuża, Adrianna M; Mukherjee, Soumya; Wang, Shi-Qiang; O'Hearn, Daniel J; Zaworotko, Michael J.
[Cu(4-phenylpyridine)<sub>4</sub>(trifluoromethanesulfonate)<sub>2</sub>], a Werner complex that exhibits high selectivity for o-xylene.
Chemical communications (Cambridge, England), 2020, 56, 1940-1943
7126107 CIFC12 H18 Ag3 F2 O2 S2I 21 21 2111.3195; 22.5808; 23.2576
90; 90; 90		5944.7Wang, Jia-Yin; Li, Wen-Hua; Wei, Zhong; Zhang, Chong; Li, Ya-Hui; Dong, Xi-Yan; Xu, Gang; Zang, Shuang-Quan
A hydrophobic semiconducting metal-organic framework assembled from silver chalcogenide wires.
Chemical communications (Cambridge, England), 2020, 56, 2091-2094
7126108 CIFC46 H38 N4P 1 21/c 122.5463; 7.4089; 22.2178
90; 109.269; 90		3503.4Chai, Danyang; Zeng, Xuan; Su, Xiaoxuan; Zhou, Changjiang; Zou, Yang; Zhong, Cheng; Gong, Shaolong; Yang, Chuluo
A simple and effective strategy to lock the quasi-equatorial conformation of acridine by H-H repulsion for highly efficient thermally activated delayed fluorescence emitters.
Chemical communications (Cambridge, England), 2020, 56, 2308-2311
7126109 CIFC45 H37 N5P -16.0216; 15.6695; 18.6718
99.624; 90.21; 95.366		1729Chai, Danyang; Zeng, Xuan; Su, Xiaoxuan; Zhou, Changjiang; Zou, Yang; Zhong, Cheng; Gong, Shaolong; Yang, Chuluo
A simple and effective strategy to lock the quasi-equatorial conformation of acridine by H-H repulsion for highly efficient thermally activated delayed fluorescence emitters.
Chemical communications (Cambridge, England), 2020, 56, 2308-2311
7126110 CIFC26 H25 Br N2 O6 S2P 1 21 18.6142; 15.2562; 10.0113
90; 93.761; 90		1312.9Wu, Ju; Abou-Hamdan, Hussein; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Electrochemical synthesis of 3a-bromofuranoindolines and 3a-bromopyrroloindolines mediated by MgBr<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 1713-1716
7126111 CIFC6 H21 Bi Cl9 N3P -18.181; 11.7216; 11.8724
104.188; 93.217; 108.402		1036.24Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126112 CIFC6 H21 Bi Br6 Cl3 N3P -18.3218; 12.1968; 12.2353
104.697; 108.11; 93.253		1129.25Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126113 CIFC6 H24 Bi Cl6 N3C 1 2/m 121.162; 7.9735; 11.8046
90; 104.186; 90		1931.1Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126114 CIFC6 H21 Bi Cl9 N3C 1 2/m 122.52; 8.2945; 12.1353
90; 106.123; 90		2177.6Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126115 CIFC6 H24 Bi Br6 N3P 1 2/c 111.773; 8.0673; 22.7281
90; 103.72; 90		2097.04Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126116 CIFC6 H24 Bi Br6 N3C 1 2/m 122.444; 8.1886; 11.9852
90; 104.248; 90		2134.9Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126117 CIFC6 H24 Bi I6 N3P 1 21/c 18.952; 29.5398; 11.8481
90; 93.269; 90		3128.02Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126118 CIFC6 Bi Cl3 I6 N3C 1 2/m 126.2181; 8.6303; 13.2652
90; 110.247; 90		2816.1Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126119 CIFC6 Bi Cl3 I6 N3P -18.5701; 12.4903; 12.9228
103.943; 108.815; 93.035		1257.88Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126120 CIFC6 H24 Bi Cl6 N3P 1 2/c 111.5267; 7.8653; 21.5333
90; 103.831; 90		1895.62Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126121 CIFC6 H21 Bi Br6 Cl3 N3C 1 2/m 124.29; 8.274; 12.4821
90; 108.894; 90		2373.4Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126122 CIFC25 H24 Cl N SiP -18.346; 9.916; 13.969
86.705; 77.173; 71.341		1067.8Zeng, Ya-Li; Chen, Bo; Wang, Ya-Ting; He, Cheng-Yu; Mu, Zi-Yuan; Du, Ji-Yuan; He, Long; Chu, Wen-Dao; Liu, Quan-Zhong
Copper-catalyzed asymmetric silyl addition to alkenyl-substituted N-heteroarenes.
Chemical communications (Cambridge, England), 2020, 56, 1693-1696
7126123 CIFIn3 La3 O3 S6P m c n3.985; 20.546; 14.8477
90; 90; 90		1215.67Kabbour, Houria; Sayede, Adlane; Saitzek, Sébastien; Lefèvre, Gauthier; Cario, Laurent; Trentesaux, Martine; Roussel, Pascal
Structure of the water-splitting photocatalyst oxysulfide α-LaOInS<sub>2</sub> and ab initio prediction of new polymorphs.
Chemical communications (Cambridge, England), 2020, 56, 1645-1648
7126124 CIFC18 H13 NF d d 238.272; 12.8163; 10.858
90; 90; 90		5325.9Liu, Xiaobing; Sheng, Heyun; Zhou, Yao; Song, Qiuling
Palladium-catalyzed C-H bond activation for the assembly of N-aryl carbazoles with aromatic amines as nitrogen sources.
Chemical communications (Cambridge, England), 2020, 56, 1665-1668
7126125 CIFC30 H20 N2P 21 21 219.0542; 12.4973; 18.9834
90; 90; 90		2148.03Liu, Xiaobing; Sheng, Heyun; Zhou, Yao; Song, Qiuling
Palladium-catalyzed C-H bond activation for the assembly of N-aryl carbazoles with aromatic amines as nitrogen sources.
Chemical communications (Cambridge, England), 2020, 56, 1665-1668
7126126 CIFC42 H36 O2I 1 2/a 112.3667; 16.1708; 15.3924
90; 108.863; 90		2912.85Lin, Wei-Bin; He, Dong-Qiang; Lu, Hai-Yan; Hu, Zhi-Qiang; Chen, Chuan-Feng
Sign inversions of circularly polarized luminescence for helical compounds by chemically fine-tuning operations.
Chemical communications (Cambridge, England), 2020, 56, 1863-1866
7126127 CIFC40 H30 Cl2 O2I 1 2/a 112.4619; 16.5737; 15.2124
90; 103.676; 90		3052.89Lin, Wei-Bin; He, Dong-Qiang; Lu, Hai-Yan; Hu, Zhi-Qiang; Chen, Chuan-Feng
Sign inversions of circularly polarized luminescence for helical compounds by chemically fine-tuning operations.
Chemical communications (Cambridge, England), 2020, 56, 1863-1866
7126128 CIFC108 H68 N4 O40 Zr6C m m m20.7974; 34.3196; 24.2844
90; 90; 90		17333.2Mallick, Arijit; Liang, Hanfeng; Shekhah, Osama; Jia, Jiangtao; Mouchaham, Georges; Shkurenko, Aleksander; Belmabkhout, Youssef; Alshareef, Husam N.; Eddaoudi, Mohamed
Made-to-order porous electrodes for supercapacitors: MOFs embedded with redox-active centers as a case study.
Chemical communications (Cambridge, England), 2020, 56, 1883-1886
7126129 CIFC49 H65 Cl9 N14 O2P -112.9113; 13.8869; 16.5533
102.178; 91.521; 97.504		2871.85Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126130 CIFC56 H54 F6 N12 O2P -110.8092; 14.1679; 17.2034
78.408; 86.646; 86.284		2572.64Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126131 CIFC44 H54 Cl2 N12 O2P -110.7643; 14.0058; 15.9242
89.704; 78.054; 67.659		2165.3Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126132 CIFC25 H30 Cl4 N6 OP -110.3164; 15.7661; 18.2979
68.115; 89.376; 87.542		2759.08Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126133 CIFC22 H31 N7 OP b c a9.8856; 10.418; 42.5525
90; 90; 90		4382.4Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126134 CIFC34 H36 N6 OP -111.2953; 11.412; 13.0664
70.404; 73.213; 70.603		1466.5Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126135 CIFC33 H33 Cl N6 OP -19.1544; 10.8644; 15.5035
72.725; 84.894; 83.984		1461.55Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126136 CIFC32 H35 N7 OP 1 21 16.7885; 7.9643; 26.039
90; 94.113; 90		1404.19Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126137 CIFC32 H37 N7 OP -16.3741; 9.3723; 24.838
83.121; 85.819; 79.949		1448.5Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126138 CIFC33 H33 Cl N6 OP 1 21/n 19.0985; 10.3538; 30.3383
90; 97.525; 90		2833.38Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126139 CIFC30 H32 Cl N7 OP 1 21/n 19.8002; 15.121; 19.4804
90; 90.374; 90		2886.72Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126140 CIFC42 H58 N4P -16.449; 10.347; 13.623
85.979; 84.125; 82.722		895.5Guo, Jing; Cheong, Odelia; Bamford, Karlee L.; Zhou, Jiliang; Stephan, Douglas W.
Frustrated Lewis pair-catalyzed double hydroarylation of alkynes with N-substituted pyrroles.
Chemical communications (Cambridge, England), 2020, 56, 1855-1858
7126141 CIFC48 H62 Br2 N4P 1 21/n 110.782; 13.431; 15.604
90; 97.24; 90		2241.6Guo, Jing; Cheong, Odelia; Bamford, Karlee L.; Zhou, Jiliang; Stephan, Douglas W.
Frustrated Lewis pair-catalyzed double hydroarylation of alkynes with N-substituted pyrroles.
Chemical communications (Cambridge, England), 2020, 56, 1855-1858
7126142 CIFC23 H23 I N2P 1 21/c 19.759; 14.912; 14.143
90; 104.115; 90		1996Elhussin, Imad Elddin Haj; Zhang, Sijing; Liu, Jiejie; Li, Dandan; Zhang, Qiong; Li, Shengli; Tian, Xiaohe; Wu, Jieying; Tian, Yupeng
A novel water-soluble quinoline-indole derivative as a three-photon fluorescent probe for identifying nucleolus RNA and mitochondrial DNA.
Chemical communications (Cambridge, England), 2020, 56, 1859-1862
7126143 CIFC23 H24 N2 O4 SP 1 21/c 110.532; 13.748; 14.154
90; 92.091; 90		2048Elhussin, Imad Elddin Haj; Zhang, Sijing; Liu, Jiejie; Li, Dandan; Zhang, Qiong; Li, Shengli; Tian, Xiaohe; Wu, Jieying; Tian, Yupeng
A novel water-soluble quinoline-indole derivative as a three-photon fluorescent probe for identifying nucleolus RNA and mitochondrial DNA.
Chemical communications (Cambridge, England), 2020, 56, 1859-1862
7126144 CIFC14 H8 Cl N OP b c a14.7356; 5.75805; 24.963
90; 90; 90		2118.07Shan, Xiang-Huan; Yang, Bo; Qu, Jian-Ping; Kang, Yan-Biao
CuSO<sub>4</sub>-Catalyzed dual annulation to synthesize O, S or N-containing tetracyclic heteroacenes.
Chemical communications (Cambridge, England), 2020, 56, 4063-4066
7126145 CIFC14 H8 Br N OP c a 218.28779; 5.59996; 24.2843
90; 90; 90		1127.07Shan, Xiang-Huan; Yang, Bo; Qu, Jian-Ping; Kang, Yan-Biao
CuSO<sub>4</sub>-Catalyzed dual annulation to synthesize O, S or N-containing tetracyclic heteroacenes.
Chemical communications (Cambridge, England), 2020, 56, 4063-4066
7126146 CIFC28 H29 N2 O2 PP 21 21 219.1724; 11.6412; 22.267
90; 90; 90		2377.62Lundrigan, Travis; Tien, Chieh-Hung; Robertson, Katherine N.; Speed, Alexander W. H.
Air and water stable secondary phosphine oxides as diazaphospholene precatalysts.
Chemical communications (Cambridge, England), 2020, 56, 8027-8030
7126147 CIFC H N OP 1 21 114.2375; 4.3802; 15.0293
90; 104.466; 90		907.56Hossain, Munshi Sahid; Rahaman, Sk Atiur; Hatai, Joydev; Saha, Monochura; Bandyopadhyay, Subhajit
Switching the recognition ability of a photoswitchable receptor towards phosphorylated anions.
Chemical communications (Cambridge, England), 2020, 56, 4172-4175
7126148 CIFC2.933 H3.067 Cl0.133 N0.4 O0.867P -111.7556; 13.9168; 14.9786
97.472; 106.582; 110.609		2124.5Hossain, Munshi Sahid; Rahaman, Sk Atiur; Hatai, Joydev; Saha, Monochura; Bandyopadhyay, Subhajit
Switching the recognition ability of a photoswitchable receptor towards phosphorylated anions.
Chemical communications (Cambridge, England), 2020, 56, 4172-4175
7126149 CIFC18 H14 N2 O4P 21 21 218.8208; 11.9769; 14.7126
90; 90; 90		1554.3Zhao, Sihan; Cheng, Shaobing; Liu, Hui; Zhang, Jiayan; Liu, Min; Yuan, Weicheng; Zhang, Xiaomei
Synthesis of chiral [2,3]-fused indolines through enantioselective dearomatization inverse-electron-demand Diels-Alder reaction/oxidation of indoles with 2-(2-nitrovinyl)-1,4-benzoquinone.
Chemical communications (Cambridge, England), 2020, 56, 4200-4203
7126150 CIFC18 H14 N2 O4P 21 21 218.8208; 11.9769; 14.7126
90; 90; 90		1554.3Zhao, Sihan; Cheng, Shaobing; Liu, Hui; Zhang, Jiayan; Liu, Min; Yuan, Weicheng; Zhang, Xiaomei
Synthesis of chiral [2,3]-fused indolines through enantioselective dearomatization inverse-electron-demand Diels-Alder reaction/oxidation of indoles with 2-(2-nitrovinyl)-1,4-benzoquinone.
Chemical communications (Cambridge, England), 2020, 56, 4200-4203
7126151 CIFC19 H33 F6 N2 O9 PP c c n17.7788; 19.721; 15.0786
90; 90; 90		5286.79Huang, Rui-Kang; Chen, Xiao-Xian; Xiao, Zhi-Feng; Liu, De-Xuan; Zhang, Wei-Xiong; Chen, Xiao-Ming
Enhancing switchable dielectric property for crystalline supramolecular rotor compounds by adding polar components.
Chemical communications (Cambridge, England), 2020, 56, 4114-4117
7126152 CIFC19 H33 F6 N2 O9 PP c c n16.774; 20; 15.122
90; 90; 90		5073.1Huang, Rui-Kang; Chen, Xiao-Xian; Xiao, Zhi-Feng; Liu, De-Xuan; Zhang, Wei-Xiong; Chen, Xiao-Ming
Enhancing switchable dielectric property for crystalline supramolecular rotor compounds by adding polar components.
Chemical communications (Cambridge, England), 2020, 56, 4114-4117
7126153 CIFC20 H33 F3 N2 O12 SP 1 21/c 110.0129; 18.4433; 14.9448
90; 98.44; 90		2729.98Huang, Rui-Kang; Chen, Xiao-Xian; Xiao, Zhi-Feng; Liu, De-Xuan; Zhang, Wei-Xiong; Chen, Xiao-Ming
Enhancing switchable dielectric property for crystalline supramolecular rotor compounds by adding polar components.
Chemical communications (Cambridge, England), 2020, 56, 4114-4117
7126154 CIFC20 H33 F3 N2 O12 SP 1 21/c 120.31807; 17.85897; 14.6402
90; 96.2561; 90		5280.7Huang, Rui-Kang; Chen, Xiao-Xian; Xiao, Zhi-Feng; Liu, De-Xuan; Zhang, Wei-Xiong; Chen, Xiao-Ming
Enhancing switchable dielectric property for crystalline supramolecular rotor compounds by adding polar components.
Chemical communications (Cambridge, England), 2020, 56, 4114-4117
7126155 CIFBi Cu O Se2 SrP 1 21/m 17.6529; 4.0559; 9.1405
90; 113.758; 90		259.67Luo, Mengjia; Bu, Kejun; Zhang, Xian; Huang, Jian; Wang, Ruiqi; Huang, Fuqiang
Intrinsically low thermal conductivity in a p-type semiconductor SrOCuBiSe<sub>2</sub> with a [SrO]-intercalated CuBiSe<sub>2</sub> structure.
Chemical communications (Cambridge, England), 2020, 56, 4356-4359
7126156 CIFC29 H27 Cl Mn N5 O3P b c a13.4901; 13.2578; 30.134
90; 90; 90		5389.4Liu, Yi; Guo, Jin-Han; Dao, Xiao-Yao; Zhang, Xiu-Du; Zhao, Yue; Sun, Wei-Yin
Coordination polymers with a pyridyl-salen ligand for photocatalytic carbon dioxide reduction.
Chemical communications (Cambridge, England), 2020, 56, 4110-4113
7126157 CIFC29 H27 Cl Fe N5 O3P b c a13.4819; 13.3393; 30.1323
90; 90; 90		5419Liu, Yi; Guo, Jin-Han; Dao, Xiao-Yao; Zhang, Xiu-Du; Zhao, Yue; Sun, Wei-Yin
Coordination polymers with a pyridyl-salen ligand for photocatalytic carbon dioxide reduction.
Chemical communications (Cambridge, England), 2020, 56, 4110-4113
7126158 CIFC14 H26 Cl O6 P Si3 WP 1 21/c 19.3757; 10.4164; 25.134
90; 93.912; 90		2448.9Kunzmann, Robert; Omatsu, Yamato; Schnakenburg, Gregor; Espinosa Ferao, Arturo; Yanagisawa, Tatsuya; Tokitoh, Norihiro; Streubel, Rainer
A synthetic equivalent for unknown 1,3-zwitterions? - A K/OR phosphinidenoid complex with an additional Si-Cl function.
Chemical communications (Cambridge, England), 2020, 56, 3899-3902
7126159 CIFC17 H34 N O6 P Si4 WP 1 21/c 115.8672; 16.5104; 22.0806
90; 91.193; 90		5783.3Kunzmann, Robert; Omatsu, Yamato; Schnakenburg, Gregor; Espinosa Ferao, Arturo; Yanagisawa, Tatsuya; Tokitoh, Norihiro; Streubel, Rainer
A synthetic equivalent for unknown 1,3-zwitterions? - A K/OR phosphinidenoid complex with an additional Si-Cl function.
Chemical communications (Cambridge, England), 2020, 56, 3899-3902
7126160 CIFC19 H34 N O7 P Si3 WP 21 21 219.9978; 13.3597; 21.3413
90; 90; 90		2850.5Kunzmann, Robert; Omatsu, Yamato; Schnakenburg, Gregor; Espinosa Ferao, Arturo; Yanagisawa, Tatsuya; Tokitoh, Norihiro; Streubel, Rainer
A synthetic equivalent for unknown 1,3-zwitterions? - A K/OR phosphinidenoid complex with an additional Si-Cl function.
Chemical communications (Cambridge, England), 2020, 56, 3899-3902
7126161 CIFC25 H17 Cd N2 O6P -19.7751; 11.1664; 11.1677
109.183; 114.745; 90.306		1030.98Yang, Xiao-Dong; Ma, Mei-Jing; Pang, Xin-Zhu; Chen, Yun-Rui; Rooney, David; Zhang, Jie
Synergism of photocycloaddition and photoinduced electron transfer for multi-state responsive materials with high-stability and reversibility.
Chemical communications (Cambridge, England), 2020, 56, 4126-4129
7126162 CIFC25 H17 Cd N2 O6P -19.7751; 11.1664; 11.1677
109.183; 114.745; 90.306		1030.98Levine, Andrew M.; Bu, Guanhong; Biswas, Sankarsan; Tsai, Esther H. R.; Braunschweig, Adam B.; Nannenga, Brent L.
Crystal structure and orientation of organic semiconductor thin films by microcrystal electron diffraction and grazing-incidence wide-angle X-ray scattering.
Chemical communications (Cambridge, England), 2020, 56, 4204-4207
7126163 CIFC55 H82 Au B2 K O8 P2P 1 21/c 119.9307; 14.7178; 20.3785
90; 110.812; 90		5587.7Taylor, Jordan W.; Harman, W. Hill
C[double bond, length as m-dash]O scission and reductive coupling of organic carbonyls by a redox-active diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 4480-4483
7126164 CIFC61 H88 Au B2 K O7 P2P -111.3469; 13.0442; 21.464
103.942; 95.7811; 101.004		2990.5Taylor, Jordan W.; Harman, W. Hill
C[double bond, length as m-dash]O scission and reductive coupling of organic carbonyls by a redox-active diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 4480-4483
7126165 CIFC79.12 H112.34 Au B2 K O11.15 P2P 1 21/c 114.6392; 45.535; 23.842
90; 96.0286; 90		15805Taylor, Jordan W.; Harman, W. Hill
C[double bond, length as m-dash]O scission and reductive coupling of organic carbonyls by a redox-active diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 4480-4483
7126166 CIFC50 H72 Au B2 K O8 P2P -110.0837; 14.1067; 18.4824
81.7553; 84.4017; 73.8383		2494.48Taylor, Jordan W.; Harman, W. Hill
C[double bond, length as m-dash]O scission and reductive coupling of organic carbonyls by a redox-active diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 4480-4483
7126167 CIFC6 H6 Co3 O12P 1 21/n 111.269; 9.848; 14.466
90; 91.16; 90		1605.1Song, Yoodae; Khudozhitkov, Alexander E.; Lee, Jihyun; Kang, Hyosik; Kolokolov, Daniil I.; Stepanov, Alexander G.; Yoon, Minyoung
Transformation of a proton insulator to a conductor via reversible amorphous to crystalline structure transformation of MOFs.
Chemical communications (Cambridge, England), 2020, 56, 4468-4471
7126168 CIFC6 H6 Mg3 O12P 1 21/n 111.35; 9.864; 14.566
90; 91.4; 90		1630.3Song, Yoodae; Khudozhitkov, Alexander E.; Lee, Jihyun; Kang, Hyosik; Kolokolov, Daniil I.; Stepanov, Alexander G.; Yoon, Minyoung
Transformation of a proton insulator to a conductor via reversible amorphous to crystalline structure transformation of MOFs.
Chemical communications (Cambridge, England), 2020, 56, 4468-4471
7126169 CIFC28 H19 PP 1 21/c 19.0803; 21.343; 21.376
90; 99.849; 90		4081.6Xing, Chang; Liu, Jianxun; Chen, Fang; Li, Yuanyuan; Lv, Changjian; Peng, Qiuchen; Hou, Hongwei; Li, Kai
Diphenyl-1-pyrenylphosphine: photo-triggered AIE/ACQ transition with remarkable third-order nonlinear optical signal change.
Chemical communications (Cambridge, England), 2020, 56, 4220-4223
7126170 CIFC28 H19 O PP 1 21/c 19.042; 21.62; 21.34
90; 100.14; 90		4107Xing, Chang; Liu, Jianxun; Chen, Fang; Li, Yuanyuan; Lv, Changjian; Peng, Qiuchen; Hou, Hongwei; Li, Kai
Diphenyl-1-pyrenylphosphine: photo-triggered AIE/ACQ transition with remarkable third-order nonlinear optical signal change.
Chemical communications (Cambridge, England), 2020, 56, 4220-4223
7126171 CIFC60 H41 F8 N5 O RuP 21 21 2110.8463; 20.3999; 21.4989
90; 90; 90		4756.92Shing, Ka-Pan; Wan, Qingyun; Chang, Xiao-Yong; Che, Chi-Ming
The first crystallographically characterised ruthenium(vi) alkylimido porphyrin competent for aerobic epoxidation and hydrogen atom abstraction.
Chemical communications (Cambridge, England), 2020, 56, 4428-4431
7126172 CIFC64 H54 F8 N6 RuC 1 2/c 128.865; 12.4422; 18.7711
90; 128.307; 90		5290.1Shing, Ka-Pan; Wan, Qingyun; Chang, Xiao-Yong; Che, Chi-Ming
The first crystallographically characterised ruthenium(vi) alkylimido porphyrin competent for aerobic epoxidation and hydrogen atom abstraction.
Chemical communications (Cambridge, England), 2020, 56, 4428-4431
7126173 CIFC66 H44 F8 N6 RuP n n m12.6211; 12.9645; 17.2046
90; 90; 90		2815.12Shing, Ka-Pan; Wan, Qingyun; Chang, Xiao-Yong; Che, Chi-Ming
The first crystallographically characterised ruthenium(vi) alkylimido porphyrin competent for aerobic epoxidation and hydrogen atom abstraction.
Chemical communications (Cambridge, England), 2020, 56, 4428-4431
7126174 CIFC648 H540 Cl0 Eu8 N96 O48P 4/n :238.2; 38.2; 46.77
90; 90; 90		68249Li, Xiao-Zhen; Zhou, Li-Peng; Hu, Shao-Jun; Cai, Li-Xuan; Guo, Xiao-Qing; Wang, Zhuo; Sun, Qing-Fu
Metal ion adaptive self-assembly of photoactive lanthanide-based supramolecular hosts.
Chemical communications (Cambridge, England), 2020, 56, 4416-4419
7126175 CIFC18 H14 F6 N2 O2C 2 2 2110.8529; 12.6448; 13.8015
90; 90; 90		1894Breising, Valentina M.; Kayser, Jacob M.; Kehl, Anton; Schollmeyer, Dieter; Liermann, Johannes C.; Waldvogel, Siegfried R.
Electrochemical formation of N,N'-diarylhydrazines by dehydrogenative N-N homocoupling reaction.
Chemical communications (Cambridge, England), 2020, 56, 4348-4351
7126176 CIFC51 H39 N6 O16 Tb2P n a 2112.071; 33.798; 11.609
90; 90; 90		4736.2Yue, Dan; Wang, Yanyan; Chen, Dong; Wang, Zhenling
Solvent triggering structural changes for two terbium-based metal-organic frameworks and their photoluminescence sensing.
Chemical communications (Cambridge, England), 2020, 56, 4320-4323
7126177 CIFC18 H11 N2 O6 TbP 1 21/c 117.4278; 12.1359; 7.4214
90; 92.644; 90		1567.97Yue, Dan; Wang, Yanyan; Chen, Dong; Wang, Zhenling
Solvent triggering structural changes for two terbium-based metal-organic frameworks and their photoluminescence sensing.
Chemical communications (Cambridge, England), 2020, 56, 4320-4323
7126178 CIFC30 H16 N6I -4 2 d22.3365; 22.3365; 9.9167
90; 90; 90		4947.63Otani, Takashi; Sasayama, Takuma; Iwashimizu, Chisaki; Kanyiva, Kyalo Stephen; Kawai, Hidetoshi; Shibata, Takanori
Short-step synthesis and chiroptical properties of polyaza[5]-[9]helicenes with blue to green-colour emission.
Chemical communications (Cambridge, England), 2020, 56, 4484-4487
7126179 CIFC16 H10 N4P 1 n 111.6524; 4; 14.3571
90; 92.273; 90		668.65Otani, Takashi; Sasayama, Takuma; Iwashimizu, Chisaki; Kanyiva, Kyalo Stephen; Kawai, Hidetoshi; Shibata, Takanori
Short-step synthesis and chiroptical properties of polyaza[5]-[9]helicenes with blue to green-colour emission.
Chemical communications (Cambridge, England), 2020, 56, 4484-4487
7126180 CIFC25 H15 Cl3 N4P 21 21 2111.21; 17.1917; 19.618
90; 90; 90		3780.76Otani, Takashi; Sasayama, Takuma; Iwashimizu, Chisaki; Kanyiva, Kyalo Stephen; Kawai, Hidetoshi; Shibata, Takanori
Short-step synthesis and chiroptical properties of polyaza[5]-[9]helicenes with blue to green-colour emission.
Chemical communications (Cambridge, England), 2020, 56, 4484-4487
7126181 CIFC44 H28 N4 S8P -111.4592; 12.9511; 16.7818
67.616; 88.901; 64.349		2044Anderson, Christopher L.; Liang, Jiatao; Teat, Simon J.; Garzón-Ruiz, Andrés; Nenon, David P.; Navarro, Amparo; Liu, Yi
A highly substituted pyrazinophane generated from a quinoidal system via a cascade reaction.
Chemical communications (Cambridge, England), 2020, 56, 4472-4475
7126182 CIFC22 H16 N2 S4P 1 21/n 15.4963; 10.4093; 17.0568
90; 98.615; 90		964.85Anderson, Christopher L.; Liang, Jiatao; Teat, Simon J.; Garzón-Ruiz, Andrés; Nenon, David P.; Navarro, Amparo; Liu, Yi
A highly substituted pyrazinophane generated from a quinoidal system via a cascade reaction.
Chemical communications (Cambridge, England), 2020, 56, 4472-4475
7126183 CIFC39 H25 Cl2 N3 O2P -19.4415; 11.5767; 15.2148
91.73; 103.575; 110.232		1505.45Zhang, Liang; Li, Meng; Gao, Qing-Yu; Chen, Chuan-Feng
An ultralong room-temperature phosphorescent material based on the combination of small singlet-triplet splitting energy and H-aggregation.
Chemical communications (Cambridge, England), 2020, 56, 4296-4299
7126184 CIFC38 H23 N3 O2P 4115.82204; 15.82204; 44.7484
90; 90; 90		11202.2Zhang, Liang; Li, Meng; Gao, Qing-Yu; Chen, Chuan-Feng
An ultralong room-temperature phosphorescent material based on the combination of small singlet-triplet splitting energy and H-aggregation.
Chemical communications (Cambridge, England), 2020, 56, 4296-4299
7126185 CIFC59.56 H40 B12 I0.44 N11.57 P2P 1 21/n 114.8599; 14.7377; 15.2073
90; 109.961; 90		3130.3Mayer, Martin; Rohdenburg, Markus; van Lessen, Valentin; Nierstenhöfer, Marc C; Aprà, Edoardo; Grabowsky, Simon; Asmis, Knut R.; Jenne, Carsten; Warneke, Jonas
First steps towards a stable neon compound: observation and bonding analysis of [B<sub>12</sub>(CN)<sub>11</sub>Ne]<sup/>.
Chemical communications (Cambridge, England), 2020, 56, 4591-4594
7126186 CIFC17 H22 B F I N O6P 1 21/c 117.3516; 11.231; 10.6444
90; 106.111; 90		1992.86Zeng, Yao-Fu; Liu, Xu-Ge; Tan, Dong-Hang; Fan, Wen-Xin; Li, Yi-Na; Guo, Yu; Wang, Honggen
Halohydroxylation of alkenyl MIDA boronates: switchable stereoselectivity induced by B(MIDA) substituent.
Chemical communications (Cambridge, England), 2020, 56, 4332-4335
7126187 CIFC14 H17 B Br N O5C 1 2/c 121.4754; 6.47129; 24.0236
90; 114.374; 90		3041.07Zeng, Yao-Fu; Liu, Xu-Ge; Tan, Dong-Hang; Fan, Wen-Xin; Li, Yi-Na; Guo, Yu; Wang, Honggen
Halohydroxylation of alkenyl MIDA boronates: switchable stereoselectivity induced by B(MIDA) substituent.
Chemical communications (Cambridge, England), 2020, 56, 4332-4335
7126188 CIFC150 H130 Cl4 Co3 N24 O24A e a 213.2673; 66.3212; 19.2434
90; 90; 90		16932.3Wang, Hao; Sayed, Sayed Youssef; Zhou, Yuqiao; Olsen, Brian C.; Luber, Erik J.; Buriak, Jillian M.
Water-soluble pH-switchable cobalt complexes for aqueous symmetric redox flow batteries.
Chemical communications (Cambridge, England), 2020, 56, 3605-3608
7126189 CIFC28 H19 N3P 1 21/c 15.182; 16.682; 22.341
90; 95.945; 90		1920.9Ishi-I, Tsutomu; Tanaka, Honoka; Park, In Seob; Yasuda, Takuma; Kato, Shin-Ichiro; Ito, Mitsunori; Hiyoshi, Hidetaka; Matsumoto, Taisuke
White-light emission from a pyrimidine-carbazole conjugate with tunable phosphorescence-fluorescence dual emission and multicolor emission switching.
Chemical communications (Cambridge, England), 2020, 56, 4051-4054
7126190 CIFC28 H17 Cl2 N3P 1 21/n 15.421; 15.895; 24.997
90; 94.464; 90		2147Ishi-I, Tsutomu; Tanaka, Honoka; Park, In Seob; Yasuda, Takuma; Kato, Shin-Ichiro; Ito, Mitsunori; Hiyoshi, Hidetaka; Matsumoto, Taisuke
White-light emission from a pyrimidine-carbazole conjugate with tunable phosphorescence-fluorescence dual emission and multicolor emission switching.
Chemical communications (Cambridge, England), 2020, 56, 4051-4054
7126191 CIFC28 H17 Br2 N3I 1 2/a 17.5013; 12.4477; 23.8886
90; 95.423; 90		2220.6Ishi-I, Tsutomu; Tanaka, Honoka; Park, In Seob; Yasuda, Takuma; Kato, Shin-Ichiro; Ito, Mitsunori; Hiyoshi, Hidetaka; Matsumoto, Taisuke
White-light emission from a pyrimidine-carbazole conjugate with tunable phosphorescence-fluorescence dual emission and multicolor emission switching.
Chemical communications (Cambridge, England), 2020, 56, 4051-4054
7126192 CIFC28 H17 Br2 N3P 1 21/n 15.3634; 15.7657; 25.1499
90; 94.964; 90		2118.64Ishi-I, Tsutomu; Tanaka, Honoka; Park, In Seob; Yasuda, Takuma; Kato, Shin-Ichiro; Ito, Mitsunori; Hiyoshi, Hidetaka; Matsumoto, Taisuke
White-light emission from a pyrimidine-carbazole conjugate with tunable phosphorescence-fluorescence dual emission and multicolor emission switching.
Chemical communications (Cambridge, England), 2020, 56, 4051-4054
7126193 CIFC29.75 H19 Br2 N3P 1 21/n 119.6547; 5.3445; 43.593
90; 97.224; 90		4542.9Ishi-I, Tsutomu; Tanaka, Honoka; Park, In Seob; Yasuda, Takuma; Kato, Shin-Ichiro; Ito, Mitsunori; Hiyoshi, Hidetaka; Matsumoto, Taisuke
White-light emission from a pyrimidine-carbazole conjugate with tunable phosphorescence-fluorescence dual emission and multicolor emission switching.
Chemical communications (Cambridge, England), 2020, 56, 4051-4054
7126194 CIFC12 H22 N10 O18 ThP b c n9.8581; 18.755; 14.3424
90; 90; 90		2651.75Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126195 CIFC8 H12 N6 O8 UP -17.5785; 7.5951; 7.6538
117.032; 102.909; 92.179		377.53Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126196 CIFC6 H8 N6 O8 UP 1 21/n 19.1942; 5.8616; 12.1915
90; 91.678; 90		656.75Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126197 CIFC16 H25 N13 O15 ThC 1 2/c 115.7287; 12.981; 14.2585
90; 98.8468; 90		2876.6Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126198 CIFC6 H11 N5 O11 UP 1 21/c 18.5201; 9.1476; 20.323
90; 97.003; 90		1572.1Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126199 CIFC12 H22 N10 O18 ThP c c n9.7722; 11.8036; 23.0503
90; 90; 90		2658.79Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126200 CIFC21 H23 N10 O19 U2P -111.52; 12.224; 12.375
88.974; 72.739; 85.516		1659.1Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126201 CIFC16 H13 Br Fe N4 O3P -18.045; 8.9535; 12.195
96.322; 91.386; 92.148		872.11Wright, Mark A.; Wooldridge, Tyler; O'Connell, Maria A; Wright, Joseph A.
Ferracyclic carbonyl complexes as anti-inflammatory agents.
Chemical communications (Cambridge, England), 2020, 56, 4300-4303
7126202 CIFC39 H51 Fe2 N4 O20.5 S2C 1 2 123.8608; 13.3771; 15.4092
90; 101.705; 90		4816.2Wright, Mark A.; Wooldridge, Tyler; O'Connell, Maria A; Wright, Joseph A.
Ferracyclic carbonyl complexes as anti-inflammatory agents.
Chemical communications (Cambridge, England), 2020, 56, 4300-4303
7126203 CIFC39 H24 Cl4 N2 OI b a 238.6912; 13.8512; 12.528
90; 90; 90		6714Wu, Shaonan; Wang, Zhuo; Bao, Yinwei; Chen, Chen; Liu, Kun; Zhu, Bolin
A novel approach for rhodium(iii)-catalyzed C-H functionalization of 2,2'-bipyridine derivatives with alkynes: a significant substituent effect.
Chemical communications (Cambridge, England), 2020, 56, 4408-4411
7126204 CIFC20 H26 Br Cl2 N2 O2 RhP b c n29.056; 9.526; 33.069
90; 90; 90		9153Wu, Shaonan; Wang, Zhuo; Bao, Yinwei; Chen, Chen; Liu, Kun; Zhu, Bolin
A novel approach for rhodium(iii)-catalyzed C-H functionalization of 2,2'-bipyridine derivatives with alkynes: a significant substituent effect.
Chemical communications (Cambridge, England), 2020, 56, 4408-4411
7126205 CIFC38 H25 Br N2P b c a21.018; 10.048; 27.166
90; 90; 90		5737Wu, Shaonan; Wang, Zhuo; Bao, Yinwei; Chen, Chen; Liu, Kun; Zhu, Bolin
A novel approach for rhodium(iii)-catalyzed C-H functionalization of 2,2'-bipyridine derivatives with alkynes: a significant substituent effect.
Chemical communications (Cambridge, England), 2020, 56, 4408-4411
7126206 CIFC20 H21 Br Cl N2 RhP -18.968; 11.141; 11.249
65.119; 83.659; 80.437		1004.4Wu, Shaonan; Wang, Zhuo; Bao, Yinwei; Chen, Chen; Liu, Kun; Zhu, Bolin
A novel approach for rhodium(iii)-catalyzed C-H functionalization of 2,2'-bipyridine derivatives with alkynes: a significant substituent effect.
Chemical communications (Cambridge, England), 2020, 56, 4408-4411
7126207 CIFC34 H31 Br Cl N2 RhP 1 21/c 111.4817; 20.8558; 14.978
90; 111.615; 90		3334.4Wu, Shaonan; Wang, Zhuo; Bao, Yinwei; Chen, Chen; Liu, Kun; Zhu, Bolin
A novel approach for rhodium(iii)-catalyzed C-H functionalization of 2,2'-bipyridine derivatives with alkynes: a significant substituent effect.
Chemical communications (Cambridge, England), 2020, 56, 4408-4411
7126208 CIFC3 H10 N4 O3P 1 21/c 19.1606; 9.7305; 7.8691
90; 102.839; 90		683.89Guan, Ruifang; Dong, Baoli; Xu, Cui; Zhang, Hao; Cao, Duxia; Lin, Weiying
A strategy to construct fluorescent non-aromatic small-molecules: hydrogen bonds contributing to the unexpected fluorescence.
Chemical communications (Cambridge, England), 2020, 56, 4424-4427
7126209 CIFC14 H16 O2P 21 21 218.4235; 10.6627; 12.6898
90; 90; 90		1139.76Zhou, Pan; Xu, Tao
Nickel-catalyzed intramolecular desymmetrization addition of aryl halides to 1,3-diketones.
Chemical communications (Cambridge, England), 2020, 56, 8194-8197
7126210 CIFC44 H46 Fe N2 O2P 1 21/c 117.7; 10.2249; 20.534
90; 101.099; 90		3646.7Kephart, Jonathan A.; Hecht, Zachary; Livesay, Brooke N.; Bhowmick, Indrani; Shores, Matthew P.; Popescu, V. Codrina; Arulsamy, Navamoney; Hulley, Elliott B.
Self-assembly of an organometallic Fe<sub>9</sub>O<sub>6</sub> cluster from aerobic oxidation of (tmeda)Fe(CH<sub>2</sub><sup>t</sup>Bu)<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 4994-4997
7126211 CIFC53 H126 Fe9 N6 O6R 3 2 :H16.9429; 16.9429; 23.233
90; 90; 120		5775.8Kephart, Jonathan A.; Hecht, Zachary; Livesay, Brooke N.; Bhowmick, Indrani; Shores, Matthew P.; Popescu, V. Codrina; Arulsamy, Navamoney; Hulley, Elliott B.
Self-assembly of an organometallic Fe<sub>9</sub>O<sub>6</sub> cluster from aerobic oxidation of (tmeda)Fe(CH<sub>2</sub><sup>t</sup>Bu)<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 4994-4997
7126212 CIFC24 H19 Br F3 N O2P -18.262; 11.3867; 22.2514
91.776; 94.224; 94.328		2080.3Huang, Jie; Li, Feng; Cui, Lei; Su, Shikuan; Jia, Xueshun; Li, Jian
Palladium-catalyzed cascade reactions of enynones and isocyanides: access towards functionalized ketenimine and its application.
Chemical communications (Cambridge, England), 2020, 56, 4555-4558
7126213 CIFC34 H27 Br3 N2 O5P 1 21/n 110.8209; 13.1614; 23.1775
90; 103.056; 90		3215.6Huang, Jie; Li, Feng; Cui, Lei; Su, Shikuan; Jia, Xueshun; Li, Jian
Palladium-catalyzed cascade reactions of enynones and isocyanides: access towards functionalized ketenimine and its application.
Chemical communications (Cambridge, England), 2020, 56, 4555-4558
7126214 CIFC7 H25 I8 N11 Sn2P -19.353; 12.8318; 15.0588
111.452; 102.192; 91.234		1634.4McNulty, Jason A.; Lightfoot, Philip
Unprecedented tin iodide perovskite-like structures featuring ordering of organic moieties.
Chemical communications (Cambridge, England), 2020, 56, 4543-4546
7126215 CIFC3 H10 I6 N6 Sn2P 43 21 29.0746; 9.0746; 25.3561
90; 90; 90		2088McNulty, Jason A.; Lightfoot, Philip
Unprecedented tin iodide perovskite-like structures featuring ordering of organic moieties.
Chemical communications (Cambridge, England), 2020, 56, 4543-4546
7126216 CIFC47 H50 Al F36 N5 O4 SiP 1 21/m 110.8558; 19.5631; 14.1328
90; 97.318; 90		2976.98Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126217 CIFC48 H49 Al Cl2 F36 N4 O4 SiP 1 21 110.8096; 36.2399; 15.9889
90; 92.324; 90		6258.32Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126218 CIFC57 H72 Al F36 N5 O4 SnP 1 21 111.0279; 19.9344; 17.9479
90; 107.293; 90		3767.22Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126219 CIFC47 H47 Al F36 N4 O4 SiP 1 21/c 113.993; 19.5525; 21.6682
90; 98.012; 90		5870.51Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126220 CIFC51 H58 Al F36 Ge N5 O4P -111.2303; 14.7524; 20.0867
80.757; 87.515; 86.337		3276.07Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126221 CIFC47 H47 Al F36 Ge N4 O4P 1 21/c 113.9314; 19.6837; 21.7403
90; 98.072; 90		5902.59Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126222 CIFC51 H58 Al F36 N5 O4 SiP -111.1801; 14.7647; 20.0683
82.558; 87.937; 85.473		3273.4Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126223 CIFC47 H47 Al F36 N4 O4 SnP 1 21/n 116.261; 19.8055; 18.8111
90; 103.171; 90		5898.88Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126224 CIFC34 H22 F10 I2 N2 O S2P n a 2117.2715; 27.171; 7.9406
90; 90; 90		3726.4Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126225 CIFC31 H18 F10 I2 N2 O S2P n a 2117.564; 25.64; 7.07
90; 90; 90		3184Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126226 CIFC31 H16 F10 I2 N2 S2P n a 2117.723; 26.15; 7
90; 90; 90		3244Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126227 CIFC31 H16 F10 I2 N2 S2P n a 2117.556; 26.464; 7.633
90; 90; 90		3546Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126228 CIFC33.85 H24 F10 I2 N2 O2 S2P n a 2117.2451; 27.2415; 7.9554
90; 90; 90		3737.3Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126229 CIFC31 H16 F10 I2 N2 S2P n a 2117.449; 26.511; 7.536
90; 90; 90		3486Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126230 CIFC31 H18 F10 I2 N2 O S2P n a 2117.606; 25.58; 6.944
90; 90; 90		3127Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126231 CIFC31 H16 F10 I2 N2 S2P n a 2117.559; 26.315; 7.259
90; 90; 90		3354Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126232 CIFC24 H24 Cl3 F N O2 PP 1 21/c 113.7106; 10.0817; 19.9799
90; 91.438; 90		2760.88Gou, Xue-Ya; Zhang, Bo-Sheng; Wang, Xin-Gang; Shi, Wei-Yu; Liu, Hong-Chao; An, Yang; Zhang, Zhe; Liang, Yong-Min
Visible-light-induced ligand-free RuCl<sub>3</sub> catalyzed C-H phosphorylation in water.
Chemical communications (Cambridge, England), 2020, 56, 4704-4707
7126233 CIFC66 H88 Li2 N2 O5P 1 21 112.845; 16.759; 14.762
90; 107.779; 90		3026Schmidlin, Nadja M. C.; Scherer, Harald; Hoffmann, Anke; Böttcher, Tobias
Isolation and characterization of a lithiated pyridine - aggregation in the solid state and in solution.
Chemical communications (Cambridge, England), 2020, 56, 4160-4163
7126234 CIFC16 H16 O6P 1 21/n 18.17188; 12.40101; 13.7935
90; 91.4883; 90		1397.36Chen, Guo-Dong; Hu, Dan; Huang, Mei-Juan; Tang, Jia; Wang, Xiao-Xia; Zou, Jian; Xie, Jun; Zhang, Wei-Guang; Guo, Liang-Dong; Yao, Xin-Sheng; Abe, Ikuro; Gao, Hao
Sporormielones A-E, bioactive novel C-C coupled orsellinic acid derivative dimers, and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 4607-4610
7126235 CIFC16 H16 O6P 21 21 219.1094; 10.3354; 14.8756
90; 90; 90		1400.53Chen, Guo-Dong; Hu, Dan; Huang, Mei-Juan; Tang, Jia; Wang, Xiao-Xia; Zou, Jian; Xie, Jun; Zhang, Wei-Guang; Guo, Liang-Dong; Yao, Xin-Sheng; Abe, Ikuro; Gao, Hao
Sporormielones A-E, bioactive novel C-C coupled orsellinic acid derivative dimers, and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 4607-4610
7126236 CIFC16 H18 O7P 1 21/c 113.4502; 7.6047; 15.7124
90; 110.641; 90		1504Chen, Guo-Dong; Hu, Dan; Huang, Mei-Juan; Tang, Jia; Wang, Xiao-Xia; Zou, Jian; Xie, Jun; Zhang, Wei-Guang; Guo, Liang-Dong; Yao, Xin-Sheng; Abe, Ikuro; Gao, Hao
Sporormielones A-E, bioactive novel C-C coupled orsellinic acid derivative dimers, and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 4607-4610
7126237 CIFC16 H16 O6P 1 21/n 18.519; 16.0695; 10.3653
90; 102.495; 90		1385.4Chen, Guo-Dong; Hu, Dan; Huang, Mei-Juan; Tang, Jia; Wang, Xiao-Xia; Zou, Jian; Xie, Jun; Zhang, Wei-Guang; Guo, Liang-Dong; Yao, Xin-Sheng; Abe, Ikuro; Gao, Hao
Sporormielones A-E, bioactive novel C-C coupled orsellinic acid derivative dimers, and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 4607-4610
7126238 CIFC16 H16 O6P 1 21/n 19.17259; 11.667; 12.81692
90; 98.1439; 90		1357.79Chen, Guo-Dong; Hu, Dan; Huang, Mei-Juan; Tang, Jia; Wang, Xiao-Xia; Zou, Jian; Xie, Jun; Zhang, Wei-Guang; Guo, Liang-Dong; Yao, Xin-Sheng; Abe, Ikuro; Gao, Hao
Sporormielones A-E, bioactive novel C-C coupled orsellinic acid derivative dimers, and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 4607-4610
7126239 CIFC65 H72 B F24 P2 RhP 1 21/n 119.0415; 17.9747; 19.5602
90; 91.7586; 90		6691.62Bukvic, Alexander J.; Crivoi, Dana Georgiana; Garwood, Hollie G.; McKay, Alasdair I.; Chen, Thomas T. D.; Martínez-Martínez, Antonio J; Weller, Andrew S.
Tolerant to air σ-alkane complexes by surface modification of single crystalline solid-state molecular organometallics using vapour-phase cationic polymerisation: SMOM@polymer.
Chemical communications (Cambridge, England), 2020, 56, 4328-4331
7126240 CIFC61 H66 B F24 P2 RhP -112.8015; 12.9012; 19.8814
91.347; 90.717; 96.597		3260.5Bukvic, Alexander J.; Crivoi, Dana Georgiana; Garwood, Hollie G.; McKay, Alasdair I.; Chen, Thomas T. D.; Martínez-Martínez, Antonio J; Weller, Andrew S.
Tolerant to air σ-alkane complexes by surface modification of single crystalline solid-state molecular organometallics using vapour-phase cationic polymerisation: SMOM@polymer.
Chemical communications (Cambridge, England), 2020, 56, 4328-4331
7126241 CIFC62 H70 B F24 O P2 RhP -112.877; 13.5514; 19.2488
91.699; 95.671; 98.347		3303.8Bukvic, Alexander J.; Crivoi, Dana Georgiana; Garwood, Hollie G.; McKay, Alasdair I.; Chen, Thomas T. D.; Martínez-Martínez, Antonio J; Weller, Andrew S.
Tolerant to air σ-alkane complexes by surface modification of single crystalline solid-state molecular organometallics using vapour-phase cationic polymerisation: SMOM@polymer.
Chemical communications (Cambridge, England), 2020, 56, 4328-4331
7126242 CIFC40 H104 B4 Na2 O2 Si8 Y2P -110.929; 16.497; 17.2819
90.747; 90.198; 92		3113.7Durrant, James P.; Tang, Jinkui; Mansikkamäki, Akseli; Layfield, Richard A.
Enhanced single-molecule magnetism in dysprosium complexes of a pristine cyclobutadienyl ligand.
Chemical communications (Cambridge, England), 2020, 56, 4708-4711
7126243 CIFC40 H104 B4 Dy2 Na2 O2 Si8P -110.9592; 16.5329; 17.2892
90.676; 90.257; 92.791		3128.6Durrant, James P.; Tang, Jinkui; Mansikkamäki, Akseli; Layfield, Richard A.
Enhanced single-molecule magnetism in dysprosium complexes of a pristine cyclobutadienyl ligand.
Chemical communications (Cambridge, England), 2020, 56, 4708-4711
7126244 CIFC20 H52 B2 Dy K O Si4P 1 21/n 110.846; 17.5547; 16.9092
90; 91.916; 90		3217.68Durrant, James P.; Tang, Jinkui; Mansikkamäki, Akseli; Layfield, Richard A.
Enhanced single-molecule magnetism in dysprosium complexes of a pristine cyclobutadienyl ligand.
Chemical communications (Cambridge, England), 2020, 56, 4708-4711
7126245 CIFC20 H52 B2 K O Si4 YP 1 21/n 110.7817; 17.5986; 16.9013
90; 91.955; 90		3205.03Durrant, James P.; Tang, Jinkui; Mansikkamäki, Akseli; Layfield, Richard A.
Enhanced single-molecule magnetism in dysprosium complexes of a pristine cyclobutadienyl ligand.
Chemical communications (Cambridge, England), 2020, 56, 4708-4711
7126246 CIFC30 H19 B F20 Ge O2P b c a14.3032; 17.5925; 24.968
90; 90; 90		6282.7Talavera, Maria; Meißner, Gisa; Rachor, Simon G.; Braun, Thomas
C-F activation reactions at germylium ions: dehydrofluorination of fluoralkanes.
Chemical communications (Cambridge, England), 2020, 56, 4452-4455
7126247 CIFC14 H13 N O4 SP 1 21 17.7349; 9.6402; 9.3298
90; 101.782; 90		681Liu, Gongyi; Zhang, Xianghe; Wang, Heng; Cong, Hengjiang; Zhang, Xumu; Dong, Xiu-Qin
Synthesis of chiral α-substituted α-amino acid and amine derivatives through Ni-catalyzed asymmetric hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 4934-4937
7126248 CIFC9 H11 N O5 SP 31 2 17.1576; 7.1576; 37.3509
90; 90; 120		1657.17Liu, Gongyi; Zhang, Xianghe; Wang, Heng; Cong, Hengjiang; Zhang, Xumu; Dong, Xiu-Qin
Synthesis of chiral α-substituted α-amino acid and amine derivatives through Ni-catalyzed asymmetric hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 4934-4937
7126249 CIFC22 H14 N2 O5P 1 21/n 112.7979; 5.74316; 22.89076
90; 92.3207; 90		1681.1Aizawa, Takumi; Aratsu, Keisuke; Datta, Sougata; Mashimo, Takaki; Seki, Tomohiro; Kajitani, Takashi; Silly, Fabien; Yagai, Shiki
Hydrogen bond-directed supramolecular polymorphism leading to soft and hard molecular ordering.
Chemical communications (Cambridge, England), 2020, 56, 4280-4283
7126250 CIFC4 H12 Cl2 Ga NP -4 21 m9.2755; 9.2755; 5.8368
90; 90; 90		502.17Wu, Qi; Liu, Xian; Du, Yeshuang; Teng, Chunlin; Liang, Fei
Nonlinear organic-inorganic halide hybrids containing unprecedented linear [MIX<sub>2</sub>]<sup>-</sup> coordination units and quasi-two-dimensional lone pairs.
Chemical communications (Cambridge, England), 2020, 56, 4894-4897
7126251 CIFC4 H12 Cl2 In NP -4 21 m9.2807; 9.2807; 5.8414
90; 90; 90		503.128Wu, Qi; Liu, Xian; Du, Yeshuang; Teng, Chunlin; Liang, Fei
Nonlinear organic-inorganic halide hybrids containing unprecedented linear [MIX<sub>2</sub>]<sup>-</sup> coordination units and quasi-two-dimensional lone pairs.
Chemical communications (Cambridge, England), 2020, 56, 4894-4897
7126252 CIFC14 H10 Cl N O SP 1 21/c 19.0173; 9.8035; 14.1588
90; 95.552; 90		1245.8Pradhan, Suman; Patel, Sandeep; Chatterjee, Indranil
Nitrosoarene-catalyzed regioselective aromatic C-H sulfinylation with thiols under aerobic conditions.
Chemical communications (Cambridge, England), 2020, 56, 5054-5057
7126253 CIFC14 H15 N O SP 1 21/c 114.275; 7.6981; 11.6398
90; 101.25; 90		1254.5Pradhan, Suman; Patel, Sandeep; Chatterjee, Indranil
Nitrosoarene-catalyzed regioselective aromatic C-H sulfinylation with thiols under aerobic conditions.
Chemical communications (Cambridge, England), 2020, 56, 5054-5057
7126254 CIFC141 H244 N12 U4P 42 21 220.7855; 20.7855; 35.3744
90; 90; 90		15283.1Boreen, Michael A.; Rao, Guodong; Villarreal, David G.; Watt, Fabian A.; Britt, R. David; Hohloch, Stephan; Arnold, John
Lewis acid capping of a uranium(v) nitride via a uranium(iii) azide molecular square.
Chemical communications (Cambridge, England), 2020, 56, 4535-4538
7126255 CIFC55.5 H62 B F15 N UP -112.5562; 13.4735; 18.1929
100.421; 97.392; 116.686		2626.3Boreen, Michael A.; Rao, Guodong; Villarreal, David G.; Watt, Fabian A.; Britt, R. David; Hohloch, Stephan; Arnold, John
Lewis acid capping of a uranium(v) nitride via a uranium(iii) azide molecular square.
Chemical communications (Cambridge, England), 2020, 56, 4535-4538
7126256 CIFC52 H40 B2 F30 N6 Na2 O4P -111.1153; 11.7453; 12.4529
70.938; 81.452; 72.255		1461.32Boreen, Michael A.; Rao, Guodong; Villarreal, David G.; Watt, Fabian A.; Britt, R. David; Hohloch, Stephan; Arnold, John
Lewis acid capping of a uranium(v) nitride via a uranium(iii) azide molecular square.
Chemical communications (Cambridge, England), 2020, 56, 4535-4538
7126257 CIFC60 H61 N5 O8P -18.9154; 9.9908; 14.3287
98.926; 91.79; 92.209		1259Ren, Demin; Koniarz, Sebastian; Li, Xiaofang; Chmielewski, Piotr J.
First imidazole-fused carbaporphyrinoid and its conversion to a N-heterocyclic carbene precursor.
Chemical communications (Cambridge, England), 2020, 56, 4836-4839
7126258 CIFC48.5 H33 Ag Au Cl4 N5P -19.9193; 13.7034; 15.7321
75.013; 84.724; 78.55		2022.72Ren, Demin; Koniarz, Sebastian; Li, Xiaofang; Chmielewski, Piotr J.
First imidazole-fused carbaporphyrinoid and its conversion to a N-heterocyclic carbene precursor.
Chemical communications (Cambridge, England), 2020, 56, 4836-4839
7126259 CIFC18 H11 Cr F9 N3 O9 S3P -113.3872; 13.4166; 15.684
81.472; 68.974; 85.355		2599.2Ma, Xiaozhou; Suturina, Elizaveta A.; Rouzières, Mathieu; Wilhelm, Fabrice; Rogalev, Andrei; Clérac, Rodolphe; Dechambenoit, Pierre
A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange.
Chemical communications (Cambridge, England), 2020, 56, 4906-4909
7126260 CIFC43 H26 Cr F6 N10 O6 S2P -19.863; 12.837; 16.567
98.505; 100.19; 98.845		2006.6Ma, Xiaozhou; Suturina, Elizaveta A.; Rouzières, Mathieu; Wilhelm, Fabrice; Rogalev, Andrei; Clérac, Rodolphe; Dechambenoit, Pierre
A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange.
Chemical communications (Cambridge, England), 2020, 56, 4906-4909
7126261 CIFC94 H75 Cr2 F6 N21 O8 S2P -110.8374; 13.4385; 15.1456
81.115; 87.233; 76.72		2120.85Ma, Xiaozhou; Suturina, Elizaveta A.; Rouzières, Mathieu; Wilhelm, Fabrice; Rogalev, Andrei; Clérac, Rodolphe; Dechambenoit, Pierre
A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange.
Chemical communications (Cambridge, England), 2020, 56, 4906-4909
7126262 CIFC46 H33 Cr F9 N9 O10 S3P -110.6856; 13.1212; 18.0622
72.344; 83.075; 86.981		2395.2Ma, Xiaozhou; Suturina, Elizaveta A.; Rouzières, Mathieu; Wilhelm, Fabrice; Rogalev, Andrei; Clérac, Rodolphe; Dechambenoit, Pierre
A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange.
Chemical communications (Cambridge, England), 2020, 56, 4906-4909
7126263 CIFC42 H50 O4 SP 1 21/c 117.0878; 10.7963; 21.0437
90; 109.074; 90		3669.1Ghotekar, Ganesh S.; Shirsath, Sachin R.; Shaikh, Aslam C.; Muthukrishnan, M.
1,6-Conjugate addition initiated formal [4+2] annulation of p-quinone methides with sulfonyl allenols: a unique access to spiro[5.5]undeca-1,4-dien-3-one scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 5022-5025
7126264 CIFC32 H31 F N2 O4 S2P 1 21/n 111.5515; 15.2491; 15.9658
90; 91.512; 90		2811.4Wang, Hao-Ran; Huang, En-He; Luo, Chen; Luo, Wen-Feng; Xu, Yin; Qian, Peng-Cheng; Zhou, Jin-Mei; Ye, Long-Wu
Copper-catalyzed tandem cis-carbometallation/cyclization of imine-ynamides with arylboronic acids.
Chemical communications (Cambridge, England), 2020, 56, 4832-4835
7126265 CIFC28 H23 N O3 SP 1 21/c 112.7799; 10.1536; 18.2019
90; 108.934; 90		2234.12Wang, Hao-Ran; Huang, En-He; Luo, Chen; Luo, Wen-Feng; Xu, Yin; Qian, Peng-Cheng; Zhou, Jin-Mei; Ye, Long-Wu
Copper-catalyzed tandem cis-carbometallation/cyclization of imine-ynamides with arylboronic acids.
Chemical communications (Cambridge, England), 2020, 56, 4832-4835
7126266 CIFC22 H16 F6 N2 O2P b c n28.1272; 9.04947; 14.7304
90; 90; 90		3749.42Lamb, Katie J.; Dowsett, Mark R.; North, Michael; Parker, Rachel R.; Whitwood, Adrian C.
Unprecedented reductive cyclisation of salophen ligands to tetrahydroquinoxalines during metal complex formation.
Chemical communications (Cambridge, England), 2020, 56, 4844-4847
7126267 CIFC20 H18 N2 O2P 1 21/n 17.16584; 10.4417; 21.8016
90; 96.8756; 90		1619.54Lamb, Katie J.; Dowsett, Mark R.; North, Michael; Parker, Rachel R.; Whitwood, Adrian C.
Unprecedented reductive cyclisation of salophen ligands to tetrahydroquinoxalines during metal complex formation.
Chemical communications (Cambridge, England), 2020, 56, 4844-4847
7126268 CIFC10 H12.67 N0.67 O1.33C 1 2/c 117.8343; 12.4405; 13.0921
90; 107.301; 90		2773.29Lamb, Katie J.; Dowsett, Mark R.; North, Michael; Parker, Rachel R.; Whitwood, Adrian C.
Unprecedented reductive cyclisation of salophen ligands to tetrahydroquinoxalines during metal complex formation.
Chemical communications (Cambridge, England), 2020, 56, 4844-4847
7126269 CIFC22 H22 N2 O4P -17.3701; 10.2836; 12.5573
97.383; 104.649; 99.61		893.22Lamb, Katie J.; Dowsett, Mark R.; North, Michael; Parker, Rachel R.; Whitwood, Adrian C.
Unprecedented reductive cyclisation of salophen ligands to tetrahydroquinoxalines during metal complex formation.
Chemical communications (Cambridge, England), 2020, 56, 4844-4847
7126270 CIFC28 H34 N2 O2P 1 21/c 116.29085; 20.8151; 23.2057
90; 105.286; 90		7590.55Lamb, Katie J.; Dowsett, Mark R.; North, Michael; Parker, Rachel R.; Whitwood, Adrian C.
Unprecedented reductive cyclisation of salophen ligands to tetrahydroquinoxalines during metal complex formation.
Chemical communications (Cambridge, England), 2020, 56, 4844-4847
7126271 CIFC120 H174 B2 Ca2 N12 O2P 1 2/c 115.552; 15.578; 45.215
90; 90.58; 90		10954Shi, Xianghui; Hou, Cuiping; Zhao, Lanxiao; Deng, Peng; Cheng, Jianhua
Mononuclear calcium complex as effective catalyst for alkenes hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 5162-5165
7126272 CIFC62 H83 B Ca N6P -111.9771; 14.8686; 16.6034
99.757; 99.777; 104.406		2751.9Shi, Xianghui; Hou, Cuiping; Zhao, Lanxiao; Deng, Peng; Cheng, Jianhua
Mononuclear calcium complex as effective catalyst for alkenes hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 5162-5165
7126273 CIFC62 H83 B Ca N6P -111.7488; 15.0579; 15.7679
96.695; 94.947; 101.734		2695.2Shi, Xianghui; Hou, Cuiping; Zhao, Lanxiao; Deng, Peng; Cheng, Jianhua
Mononuclear calcium complex as effective catalyst for alkenes hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 5162-5165
7126274 CIFC63 H93 B Ca N6 OP -114.5913; 14.6823; 15.1498
61.123; 82.567; 88.425		2815.9Shi, Xianghui; Hou, Cuiping; Zhao, Lanxiao; Deng, Peng; Cheng, Jianhua
Mononuclear calcium complex as effective catalyst for alkenes hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 5162-5165
7126275 CIFC74 H50 Cd N4 O8C 1 2/c 124.4932; 13.5736; 18.0604
90; 97.554; 90		5952.3Yang, Yongsheng; Fang, Xiaoyu; Zhao, Si-Si; Bai, Fengyang; Zhao, Zhen; Wang, Ke-Zhi; Yan, Dongpeng
One-dimensional co-crystallized coordination polymers showing reversible mechanochromic luminescence: cation-anion interaction directed rapid self-recovery.
Chemical communications (Cambridge, England), 2020, 56, 5267-5270
7126276 CIFC30 H22 Cd O6P n c a7.5033; 16.7674; 19.8262
90; 90; 90		2494.35Yang, Yongsheng; Fang, Xiaoyu; Zhao, Si-Si; Bai, Fengyang; Zhao, Zhen; Wang, Ke-Zhi; Yan, Dongpeng
One-dimensional co-crystallized coordination polymers showing reversible mechanochromic luminescence: cation-anion interaction directed rapid self-recovery.
Chemical communications (Cambridge, England), 2020, 56, 5267-5270
7126277 CIFC44 H43 N2 O12 S2P -19.2048; 15.0598; 16.5389
116.533; 90.512; 99.24		2016.11Tian, Tian; Qian, Tingjuan; Jiang, Tingting; Deng, Yakui; Li, Xiaopei; Yuan, Wei; Chen, Yulan; Wang, Yi-Xuan; Hu, Wenping
A donor-acceptor type macrocycle: toward photolyzable self-assembly.
Chemical communications (Cambridge, England), 2020, 56, 3939-3942
7126278 CIFC31 H32 Cl2 Co F6 N12 O2 PP 1 21/n 111.2862; 20.4254; 21.7177
90; 124.766; 90		4112.8Fleming, Connor; Chung, Dorothy; Ponce, Servando; Brook, David J. R.; DaRos, Jeffrey; Das, Raja; Ozarowski, Andrew; Stoian, Sebastian A.
Valence tautomerism in a cobalt-verdazyl coordination compound.
Chemical communications (Cambridge, England), 2020, 56, 4400-4403
7126279 CIFC30 H30 Co F12 N12 O2 P2P -4 21 c15.7805; 15.7805; 15.4465
90; 90; 90		3846.6Fleming, Connor; Chung, Dorothy; Ponce, Servando; Brook, David J. R.; DaRos, Jeffrey; Das, Raja; Ozarowski, Andrew; Stoian, Sebastian A.
Valence tautomerism in a cobalt-verdazyl coordination compound.
Chemical communications (Cambridge, England), 2020, 56, 4400-4403
7126280 CIFC12 H37 Ca N2 O17 P4C 1 2/c 131.0593; 5.1776; 21.8198
90; 130.591; 90		2664.6Vassaki, Maria; Papathanasiou, Konstantinos E.; Hadjicharalambous, Chrystalleni; Chandrinou, Daphne; Turhanen, Petri; Choquesillo-Lazarte, Duane; Demadis, Konstantinos D.
Self-sacrificial MOFs for ultra-long controlled release of bisphosphonate anti-osteoporotic drugs.
Chemical communications (Cambridge, England), 2020, 56, 5166-5169
7126281 CIFC12 H40 Mg N2 O18 P4P 1 21/c 114.681; 13.1202; 13.8859
90; 101.214; 90		2623.6Vassaki, Maria; Papathanasiou, Konstantinos E.; Hadjicharalambous, Chrystalleni; Chandrinou, Daphne; Turhanen, Petri; Choquesillo-Lazarte, Duane; Demadis, Konstantinos D.
Self-sacrificial MOFs for ultra-long controlled release of bisphosphonate anti-osteoporotic drugs.
Chemical communications (Cambridge, England), 2020, 56, 5166-5169
7126282 CIFC8 H28 Mg N2 O16 P4P 1 21/c 112.5897; 13.5306; 12.4892
90; 109.919; 90		2000.21Vassaki, Maria; Papathanasiou, Konstantinos E.; Hadjicharalambous, Chrystalleni; Chandrinou, Daphne; Turhanen, Petri; Choquesillo-Lazarte, Duane; Demadis, Konstantinos D.
Self-sacrificial MOFs for ultra-long controlled release of bisphosphonate anti-osteoporotic drugs.
Chemical communications (Cambridge, England), 2020, 56, 5166-5169
7126283 CIFC106 H62 F20 N8 O6 Sb2P 1 21/c 114.7806; 19.611; 32.18
90; 100.277; 90		9178.1Lemon, Christopher M.; Maher, Andrew G.; Mazzotti, Anthony R.; Powers, David C.; Gonzalez, Miguel I.; Nocera, Daniel G.
Multielectron C-H photoactivation with an Sb(v) oxo corrole.
Chemical communications (Cambridge, England), 2020, 56, 5247-5250
7126284 CIFC16 H22 Al1.33 Cl4 N2 O2C 1 2/c 122.483; 12.582; 24.213
90; 93.89; 90		6834Kore, Rajkumar; Kelley, Steven P.; Sawant, Anand D.; Mishra, Manish Kumar; Rogers, Robin D.
Are ionic liquids and liquid coordination complexes really different? - Synthesis, characterization, and catalytic activity of AlCl<sub>3</sub>/base catalysts.
Chemical communications (Cambridge, England), 2020, 56, 5362-5365
7126285 CIFC8 H12 Al2 Cl6 N4P 1 21/n 18.4788; 11.2242; 9.6038
90; 91.3763; 90		913.71Kore, Rajkumar; Kelley, Steven P.; Sawant, Anand D.; Mishra, Manish Kumar; Rogers, Robin D.
Are ionic liquids and liquid coordination complexes really different? - Synthesis, characterization, and catalytic activity of AlCl<sub>3</sub>/base catalysts.
Chemical communications (Cambridge, England), 2020, 56, 5362-5365
7126286 CIFC18 H19 N O3 SP -15.4468; 9.8135; 15.2598
103.033; 93.291; 97.938		783.72Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126287 CIFC13 H16 N O3.5 SC 1 2/c 131.768; 5.5762; 15.75
90; 108.619; 90		2644Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126288 CIFC17 H17 N O3 SP 1 21/c 116.352; 10.823; 9.736
90; 105.376; 90		1661Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126289 CIFC21 H19 N O3 SP 1 21/c 118.261; 7.799; 12.919
90; 107.2; 90		1758Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126290 CIFC17 H17 N O3 SP -15.432; 9.545; 15.32
96.31; 93.878; 97.64		779.8Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126291 CIFC18 H19 N O3 SP -15.8765; 7.649; 18.388
92.938; 94.963; 93.182		820.9Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126292 CIFC112 H98 B F4 Ir2 O4 P4P 21 21 2115.3077; 17.0493; 35.2582
90; 90; 90		9201.9Sofue, Yuki; Nomura, Kotohiro; Inagaki, Akiko
On-demand hydrogen production from formic acid by light-active dinuclear iridium catalysts.
Chemical communications (Cambridge, England), 2020, 56, 4519-4522
7126293 CIFC7 H8 Fe K N7 OP 21 21 219.8433; 8.532; 14.8241
90; 90; 90		1244.97Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126294 CIFC7 H8 Fe K N7 OP 21 21 2110.2018; 8.5037; 14.948
90; 90; 90		1296.78Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126295 CIFC7 H8 Fe K N7 OP 21 21 219.9126; 8.5286; 14.8615
90; 90; 90		1256.4Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126296 CIFC7 H8 Fe K N7 OP 21 21 2110.0838; 8.515; 14.9235
90; 90; 90		1281.38Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126297 CIFC7 H8 Fe K N7 OP n m a10.3494; 8.4866; 14.9745
90; 90; 90		1315.23Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126298 CIFC7 H8 Fe K N7 OP n m a10.4242; 8.5078; 15.0275
90; 90; 90		1332.7Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126299 CIFC7 H8 Fe K N7 OP n m a10.3262; 8.4855; 14.9627
90; 90; 90		1311.08Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126300 CIFC7 H8 Fe K N7 OP 21 21 219.9983; 8.5234; 14.8981
90; 90; 90		1269.61Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126301 CIFC7 H8 Fe K N7 OP 21 21 2110.135; 8.5134; 14.9364
90; 90; 90		1288.76Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126302 CIFC7 H8 Fe K N7 OP n m a10.3809; 8.4936; 14.9835
90; 90; 90		1321.11Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126303 CIFC7 H8 Fe K N7 OP 21 21 2110.0402; 8.5197; 14.913
90; 90; 90		1275.65Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126304 CIFC7 H8 Fe K N7 OP n m a10.3982; 8.5036; 15.0131
90; 90; 90		1327.49Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126305 CIFC11 H16 N2 O4P -16.8265; 7.2475; 13.022
87.473; 79.192; 79.227		621.65Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126306 CIFC10 H12 N2 O2P n a 218.872; 12.3858; 9.6316
90; 90; 90		1058.39Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126307 CIFC12 H10 N3 O2P n m a9.9477; 7.5082; 16.9603
90; 90; 90		1266.75Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126308 CIFC10 H13 N3 O5P -16.7495; 7.182; 14.8256
76.262; 80.534; 62.981		620.58Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126309 CIFC11 H14 N2 O2P n a 218.7406; 13.897; 9.5194
90; 90; 90		1156.3Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126310 CIFC11 H13 F3 N2 O3P 1 21/n 114.405; 6.5909; 14.669
90; 105.691; 90		1340.8Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126311 CIFC11 H11 N3 O2P 1 21/c 19.8467; 11.576; 9.697
90; 90.927; 90		1105.17Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126312 CIFC22 H16 N6P 1 21/n 17.9437; 10.9876; 10.2274
90; 90.435; 90		892.64Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126313 CIFC26 H16 Cl4 N4 O2 Zn2C 1 2/c 119.5229; 18.0694; 8.8084
90; 102.32; 90		3035.76Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126314 CIFC12 H12 Cl2 Co N4P 1 21/c 110.6519; 8.1804; 15.5453
90; 97.892; 90		1341.7Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126315 CIFC11 H8 Cl2 N2 O ZnP -18.2052; 8.6043; 9.7408
98.959; 97.49; 115.238		599.38Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126316 CIFC68 H76 Cl8 N16 S6 Sn4 Zn4P 42 21 223.7332; 23.7332; 11.4025
90; 90; 90		6422.6Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126317 CIFC68 H77 N16 O S6 Sn4P 1 2/c 115.6802; 20.3433; 12.4505
90; 109.194; 90		3750.77Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126318 CIFC35 H44 Cl4 N8 O2 Ru2 S2P -18.2648; 10.0946; 12.9476
104.143; 101.316; 100.545		996.4Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126319 CIFC79.5 H83 Cl7 N16 S6 Sn4P n a 2125.9881; 22.3278; 15.5336
90; 90; 90		9013.5Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126320 CIFC93 H95 B F24 N4 O3P 1 21/c 118.9774; 14.0644; 34.0542
90; 91.842; 90		9084.6Hsueh, Fang-Che; Tsai, Chi-You; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien
Interlocking increases the persistence of N-heterocyclic carbenes in solution.
Chemical communications (Cambridge, England), 2020, 56, 4773-4776
7126321 CIFC94.5 H99 B Cl2 F24 N4 O3.5P 1 21/n 116.4668; 21.1135; 27.6864
90; 103.746; 90		9350.1Hsueh, Fang-Che; Tsai, Chi-You; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien
Interlocking increases the persistence of N-heterocyclic carbenes in solution.
Chemical communications (Cambridge, England), 2020, 56, 4773-4776
7126322 CIFC66 H100 N4P 1 21/c 118.6997; 17.6316; 20.1905
90; 117.532; 90		5903Hsueh, Fang-Che; Tsai, Chi-You; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien
Interlocking increases the persistence of N-heterocyclic carbenes in solution.
Chemical communications (Cambridge, England), 2020, 56, 4773-4776
7126323 CIFC61 H82 N4 O3P 1 21 122.6094; 17.959; 29.4427
90; 111.156; 90		11149.2Hsueh, Fang-Che; Tsai, Chi-You; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien
Interlocking increases the persistence of N-heterocyclic carbenes in solution.
Chemical communications (Cambridge, England), 2020, 56, 4773-4776
7126324 CIFC21 H30 PtP 21 21 215.5867; 10.71; 28.421
90; 90; 90		1700.5Ernst, Lukas D.; Koessler, Konstantin; Peter, Andreas; Kratzert, Daniel; Scherer, Harald; Butschke, Burkhard
A heterodinuclear, formal Au<sup>+I</sup>Pt<sup>0</sup> complex with weakly bound alkene ligands.
Chemical communications (Cambridge, England), 2020, 56, 5350-5353
7126325 CIFC74 H63 Au B Cl6 F24 P PtP 112.7747; 12.7853; 13.1193
82.101; 88.764; 64.259		1910.06Ernst, Lukas D.; Koessler, Konstantin; Peter, Andreas; Kratzert, Daniel; Scherer, Harald; Butschke, Burkhard
A heterodinuclear, formal Au<sup>+I</sup>Pt<sup>0</sup> complex with weakly bound alkene ligands.
Chemical communications (Cambridge, England), 2020, 56, 5350-5353
7126326 CIFC71 H57 Au B F24 P PtP -112.3657; 15.5627; 19.1346
95.961; 108.064; 101.326		3378.6Ernst, Lukas D.; Koessler, Konstantin; Peter, Andreas; Kratzert, Daniel; Scherer, Harald; Butschke, Burkhard
A heterodinuclear, formal Au<sup>+I</sup>Pt<sup>0</sup> complex with weakly bound alkene ligands.
Chemical communications (Cambridge, England), 2020, 56, 5350-5353
7126327 CIFC17 H9 Cl O3P -18.2844; 8.6986; 10.7524
68.114; 78.9; 68.561		667.83Han, Xi; Kong, Lingheng; Feng, Jiami; Li, Xingwei
Rhodium(iii)-catalyzed synthesis of spirocyclic isoindole N-oxides and isobenzofuranones via C-H activation and spiroannulation.
Chemical communications (Cambridge, England), 2020, 56, 5528-5531
7126328 CIFC H N O SP 114.2587; 18.3783; 25.4318
70.965; 78.342; 79.57		6122.15Wang, Danbo; Kan, Xiaonan; Wu, Chenyu; Gong, Yuzhen; Guo, Guangming; Liang, Tongling; Wang, Lan; Li, Zhibo; Zhao, Yingjie
Charge transfer co-crystals based on donor-acceptor interactions for near-infrared photothermal conversion.
Chemical communications (Cambridge, England), 2020, 56, 5223-5226
7126329 CIFC21 H24 N2 O2 SP -16.9644; 11.4537; 11.8747
97.514; 97.294; 93.446		928.65Molina, Alba; Díaz-Tendero, Sergio; Adrio, Javier; Carretero, Juan C.
Catalytic asymmetric synthesis of diazabicyclo[3.1.0]hexanes by 1,3-dipolar cycloaddition of azomethine ylides with azirines.
Chemical communications (Cambridge, England), 2020, 56, 5050-5053
7126330 CIFC36 H30 N2 O2P -18.9247; 9.9994; 17.016
90.709; 96.541; 116.439		1347.46Molina, Alba; Díaz-Tendero, Sergio; Adrio, Javier; Carretero, Juan C.
Catalytic asymmetric synthesis of diazabicyclo[3.1.0]hexanes by 1,3-dipolar cycloaddition of azomethine ylides with azirines.
Chemical communications (Cambridge, England), 2020, 56, 5050-5053
7126331 CIFC88 H78 N4 P4 Pt2 Si2P -112.9341; 15.4591; 20.0358
70.853; 79.029; 88.937		3711.2Frogley, Benjamin J.; Hill, Anthony F.; Sharma, Manab; Sinha, Arup; Ward, Jas S.
Semi-bridging σ-silyls as Z-type ligands.
Chemical communications (Cambridge, England), 2020, 56, 3532-3535
7126332 CIFC85 H75 N4 Ni2 P4 Si2P -112.6509; 16.9249; 17.6665
81.189; 77.4286; 73.2272		3518.3Frogley, Benjamin J.; Hill, Anthony F.; Sharma, Manab; Sinha, Arup; Ward, Jas S.
Semi-bridging σ-silyls as Z-type ligands.
Chemical communications (Cambridge, England), 2020, 56, 3532-3535
7126333 CIFC88 H78 N4 P4 Pd2 Si2P -113.545; 17.6245; 17.7005
99.727; 103.685; 109.549		3724.1Frogley, Benjamin J.; Hill, Anthony F.; Sharma, Manab; Sinha, Arup; Ward, Jas S.
Semi-bridging σ-silyls as Z-type ligands.
Chemical communications (Cambridge, England), 2020, 56, 3532-3535
7126334 CIFC134 H136 Cu4 N8 O30P 1 2/n 115.2966; 17.7385; 24.6648
90; 95.051; 90		6666.5Craig, Gavin A.; Larpent, Patrick; Urabe, Hinano; Legrand, Alexandre; Bonneau, Mickaele; Kusaka, Shinpei; Furukawa, Shuhei
Hysteresis in the gas sorption isotherms of metal-organic cages accompanied by subtle changes in molecular packing.
Chemical communications (Cambridge, England), 2020, 56, 3689-3692
7126335 CIFC128.5 H124 Cu4 N7 O29P 1 21/n 114.2345; 29.3603; 16.598
90; 111.254; 90		6465Craig, Gavin A.; Larpent, Patrick; Urabe, Hinano; Legrand, Alexandre; Bonneau, Mickaele; Kusaka, Shinpei; Furukawa, Shuhei
Hysteresis in the gas sorption isotherms of metal-organic cages accompanied by subtle changes in molecular packing.
Chemical communications (Cambridge, England), 2020, 56, 3689-3692
7126336 CIFC51 H60 Cl2 N8P 1 21/c 121.9296; 9.847; 22.4505
90; 109.159; 90		4579.5Zhang, Li-Peng; Li, Xianqiang; Liu, Tianlong; Kang, Lin; Huang, Xing; Zhao, Yuxia
A water-soluble pyrazino[2,3-g]quinoxaline photosensitizer for high-efficiency one- and two-photon excited bioimaging and photodynamic therapy.
Chemical communications (Cambridge, England), 2020, 56, 5544-5547
7126337 CIFC20 H22 N2 O2P 1 21/c 118.7868; 9.84896; 19.3586
90; 108.143; 90		3403.85An, Yang; Zhang, Bo-Sheng; Zhang, Zhe; Liu, Ce; Gou, Xue-Ya; Ding, Ya-Nan; Liang, Yong-Min
A carboxylate-assisted amination/unactivated C(sp<sup>2</sup>)-H arylation reaction via a palladium/norbornene cooperative catalysis.
Chemical communications (Cambridge, England), 2020, 56, 5933-5936
7126338 CIFC19 H19 Cl N2 O3P 1 21/n 19.3251; 18.1174; 10.1704
90; 98.755; 90		1698.23An, Yang; Zhang, Bo-Sheng; Zhang, Zhe; Liu, Ce; Gou, Xue-Ya; Ding, Ya-Nan; Liang, Yong-Min
A carboxylate-assisted amination/unactivated C(sp<sup>2</sup>)-H arylation reaction via a palladium/norbornene cooperative catalysis.
Chemical communications (Cambridge, England), 2020, 56, 5933-5936
7126339 CIFC20 H22 N2 O3P -19.411; 9.7287; 9.9501
87.849; 85.541; 72.201		864.68An, Yang; Zhang, Bo-Sheng; Zhang, Zhe; Liu, Ce; Gou, Xue-Ya; Ding, Ya-Nan; Liang, Yong-Min
A carboxylate-assisted amination/unactivated C(sp<sup>2</sup>)-H arylation reaction via a palladium/norbornene cooperative catalysis.
Chemical communications (Cambridge, England), 2020, 56, 5933-5936
7126340 CIFC17 H16 F N O2P 1 21/n 117.1703; 9.1104; 19.1959
90; 115.406; 90		2712.38An, Yang; Zhang, Bo-Sheng; Zhang, Zhe; Liu, Ce; Gou, Xue-Ya; Ding, Ya-Nan; Liang, Yong-Min
A carboxylate-assisted amination/unactivated C(sp<sup>2</sup>)-H arylation reaction via a palladium/norbornene cooperative catalysis.
Chemical communications (Cambridge, England), 2020, 56, 5933-5936
7126341 CIFC17 H16 N2 OP 1 21/n 111.9106; 6.1532; 37.0164
90; 97.119; 90		2692An, Yang; Zhang, Bo-Sheng; Zhang, Zhe; Liu, Ce; Gou, Xue-Ya; Ding, Ya-Nan; Liang, Yong-Min
A carboxylate-assisted amination/unactivated C(sp<sup>2</sup>)-H arylation reaction via a palladium/norbornene cooperative catalysis.
Chemical communications (Cambridge, England), 2020, 56, 5933-5936
7126342 CIFC19 H17 Cu F6 N5 O4P 1 21/n 110.8947; 17.8622; 11.5657
90; 106.714; 90		2155.6Fukatsu, Arisa; Morimoto, Yuma; Sugimoto, Hideki; Itoh, Shinobu
Modelling a 'histidine brace' motif in mononuclear copper monooxygenases.
Chemical communications (Cambridge, England), 2020, 56, 5123-5126
7126343 CIFC25 H36.5 Br4 Fe2 N10.5 O0.5P 1 21/m 113.0724; 19.3867; 13.9064
90; 95.742; 90		3506.6Chen, Bai-Ling; Zhang, Yuan; Lei, Ya-Ru; Wang, Hui-Ming; Chen, Zili
An allenylidene Au(i) catalyst derived from triazole units and its initial application.
Chemical communications (Cambridge, England), 2020, 56, 5787-5790
7126344 CIFC29 H23 Au Cl2 N3 PP 1 21/n 111.3683; 9.5614; 24.806
90; 93.908; 90		2690.1Chen, Bai-Ling; Zhang, Yuan; Lei, Ya-Ru; Wang, Hui-Ming; Chen, Zili
An allenylidene Au(i) catalyst derived from triazole units and its initial application.
Chemical communications (Cambridge, England), 2020, 56, 5787-5790
7126345 CIFC12 H11 Au Cl N3P 1 21/n 113.575; 7.1746; 13.838
90; 106.575; 90		1291.8Chen, Bai-Ling; Zhang, Yuan; Lei, Ya-Ru; Wang, Hui-Ming; Chen, Zili
An allenylidene Au(i) catalyst derived from triazole units and its initial application.
Chemical communications (Cambridge, England), 2020, 56, 5787-5790
7126346 CIFC2.095 H1.905 B0.19 F0.762 N0.571C 1 2/c 127.272; 6.921; 14.9043
90; 116.111; 90		2526.1Chen, Bai-Ling; Zhang, Yuan; Lei, Ya-Ru; Wang, Hui-Ming; Chen, Zili
An allenylidene Au(i) catalyst derived from triazole units and its initial application.
Chemical communications (Cambridge, England), 2020, 56, 5787-5790
7126347 CIFC88 H94 B6 F6 O12C 1 2/c 118.066; 19.955; 24.133
90; 108.477; 90		8251.6Takata, Hisatsugu; Ono, Kosuke; Iwasawa, Nobuharu
Controlled release of the guest molecule via borate formation of a fluorinated boronic ester cage.
Chemical communications (Cambridge, England), 2020, 56, 5613-5616
7126348 CIFC20 H23 N3P 1 21/c 120.236; 9.7971; 17.139
90; 93.473; 90		3391.6Sathish Kumar, B.; Pati, Narendra N.; Jose, K. V. Jovan; Panda, Pradeepta K.
Synthetic access to calix[3]pyrroles via meso-expansion: hosts with diverse guest chemistry.
Chemical communications (Cambridge, England), 2020, 56, 5637-5640
7126349 CIFC24 H25 N3P 1 21/n 111.3125; 9.7429; 17.745
90; 95.103; 90		1948Sathish Kumar, B.; Pati, Narendra N.; Jose, K. V. Jovan; Panda, Pradeepta K.
Synthetic access to calix[3]pyrroles via meso-expansion: hosts with diverse guest chemistry.
Chemical communications (Cambridge, England), 2020, 56, 5637-5640
7126350 CIFC20 H27 N3 OP 1 21/n 118.2435; 11.4952; 18.5875
90; 110.086; 90		3660.9Sathish Kumar, B.; Pati, Narendra N.; Jose, K. V. Jovan; Panda, Pradeepta K.
Synthetic access to calix[3]pyrroles via meso-expansion: hosts with diverse guest chemistry.
Chemical communications (Cambridge, England), 2020, 56, 5637-5640
7126351 CIFC21 H14 Br2 N2C 1 2/c 128.82; 13.989; 18.95
90; 103.355; 90		7433Zhu, Zhongzhi; Lin, Hanze; Liang, Baihui; Huang, Junjie; Liang, Wanyi; Chen, Lu; Huang, Yubing; Chen, Xiuwen; Li, Yibiao
Copper-catalyzed [2+3]-annulation of N-H imines with vinyl azides: access to polyaryl 2H-imidazoles.
Chemical communications (Cambridge, England), 2020, 56, 5621-5624
7126352 CIFC48 H65 N O2P 1 21/n 112.1364; 17.5731; 22.0778
90; 92.7639; 90		4703.15Xue, Guodong; Hu, Xiaoguang; Chen, Hanjiao; Ge, Lingbing; Wang, Wenxiang; Xiong, Jingyuan; Miao, Fang; Zheng, Yonghao
Understanding the nature of quinoidal and zwitterionic states in carbazole-based diradicals.
Chemical communications (Cambridge, England), 2020, 56, 5143-5146
7126353 CIFC21 H13 Cl N3 SP b c a15.1373; 14.4119; 16.4702
90; 90; 90		3593.1Guo, Tao; Wei, Xu-Ning; Zhang, Miao; Liu, Yu; Zhu, Li-Min; Zhao, Yun-Hui
Catalyst and additive-free oxidative dual C-H sulfenylation of imidazoheterocycles with elemental sulfur using DMSO as a solvent and an oxidant.
Chemical communications (Cambridge, England), 2020, 56, 5751-5754
7126354 CIFC20 H17 N3 SP 21 21 218.0283; 10.563; 19.1653
90; 90; 90		1625.27Guo, Tao; Wei, Xu-Ning; Zhang, Miao; Liu, Yu; Zhu, Li-Min; Zhao, Yun-Hui
Catalyst and additive-free oxidative dual C-H sulfenylation of imidazoheterocycles with elemental sulfur using DMSO as a solvent and an oxidant.
Chemical communications (Cambridge, England), 2020, 56, 5751-5754
7126355 CIFC27 H30 N2 O3 S2P 1 21/c 113.557; 15.9431; 12.6454
90; 101.401; 90		2679.3Reddy, Angula Chandra Shekar; Ramachandran, Kuppan; Reddy, Palagulla Maheswar; Anbarasan, Pazhamalai
Rhodium-catalyzed Sommelet-Hauser type rearrangement of α-diazoimines: synthesis of functionalized enamides.
Chemical communications (Cambridge, England), 2020, 56, 5649-5652
7126356 CIFC12 H8 N2 S2P b c a6.0865; 17.576; 20.351
90; 90; 90		2177.1Huang, Guoling; Li, Jian; Ji, Xiaoliang; Chen, Lu; Liu, Qiang; Chen, Xiuwen; Huang, Yubing; Li, Yibiao
Access to 4-substituted isothiazoles through three-component cascade annulation and their application in C-H activation.
Chemical communications (Cambridge, England), 2020, 56, 5763-5766
7126357 CIFC18 H12 N2 S2I 1 2 17.8212; 5.9264; 16.1736
90; 91.155; 90		749.52Huang, Guoling; Li, Jian; Ji, Xiaoliang; Chen, Lu; Liu, Qiang; Chen, Xiuwen; Huang, Yubing; Li, Yibiao
Access to 4-substituted isothiazoles through three-component cascade annulation and their application in C-H activation.
Chemical communications (Cambridge, England), 2020, 56, 5763-5766
7126358 CIFC10 H7 N O2 SP 1 21/c 16.9853; 8.3741; 14.638
90; 99.28; 90		845.1Huang, Guoling; Li, Jian; Ji, Xiaoliang; Chen, Lu; Liu, Qiang; Chen, Xiuwen; Huang, Yubing; Li, Yibiao
Access to 4-substituted isothiazoles through three-component cascade annulation and their application in C-H activation.
Chemical communications (Cambridge, England), 2020, 56, 5763-5766
7126359 CIFC12 H12 B2 F4 N4 OP 1 21 110.2475; 4.8212; 15.131
90; 109.221; 90		705.88Pookkandam Parambil, Shandev; de Jong, Flip; Veys, Koen; Huang, Jianjun; Veettil, Santhini Pulikkal; Verhaeghe, Davy; Van Meervelt, Luc; Escudero, Daniel; Van der Auweraer, Mark; Dehaen, Wim
BOPAHY: a doubly chelated highly fluorescent pyrrole-acyl hydrazone -BF<sub>2</sub> chromophore.
Chemical communications (Cambridge, England), 2020, 56, 5791-5794
7126360 CIFC12 H11 B2 F4 N3 O2P n a 2123.933; 12.5943; 4.744
90; 90; 90		1429.93Pookkandam Parambil, Shandev; de Jong, Flip; Veys, Koen; Huang, Jianjun; Veettil, Santhini Pulikkal; Verhaeghe, Davy; Van Meervelt, Luc; Escudero, Daniel; Van der Auweraer, Mark; Dehaen, Wim
BOPAHY: a doubly chelated highly fluorescent pyrrole-acyl hydrazone -BF<sub>2</sub> chromophore.
Chemical communications (Cambridge, England), 2020, 56, 5791-5794
7126361 CIFC9 H11 B2 F4 N3 OP 1 21/c 112.9329; 4.8706; 19.777
90; 103.631; 90		1210.68Pookkandam Parambil, Shandev; de Jong, Flip; Veys, Koen; Huang, Jianjun; Veettil, Santhini Pulikkal; Verhaeghe, Davy; Van Meervelt, Luc; Escudero, Daniel; Van der Auweraer, Mark; Dehaen, Wim
BOPAHY: a doubly chelated highly fluorescent pyrrole-acyl hydrazone -BF<sub>2</sub> chromophore.
Chemical communications (Cambridge, England), 2020, 56, 5791-5794
7126362 CIFC14 H16 B2 F4 N4 OP -18.1042; 9.7049; 10.4691
80.218; 86.082; 87.104		808.9Pookkandam Parambil, Shandev; de Jong, Flip; Veys, Koen; Huang, Jianjun; Veettil, Santhini Pulikkal; Verhaeghe, Davy; Van Meervelt, Luc; Escudero, Daniel; Van der Auweraer, Mark; Dehaen, Wim
BOPAHY: a doubly chelated highly fluorescent pyrrole-acyl hydrazone -BF<sub>2</sub> chromophore.
Chemical communications (Cambridge, England), 2020, 56, 5791-5794
7126363 CIFC60.63 H55.12 B2 N5P -116.155; 17.629; 18.2
76.749; 76.424; 74.29		4773.6Prieschl, Dominic; Arrowsmith, Merle; Dietz, Maximilian; Rempel, Anna; Müller, Marcel; Braunschweig, Holger
Synthesis of polyheterocyclic 1,1-diboryltriazenes by γ-nitrogen insertion of azides into activated B-B single bonds.
Chemical communications (Cambridge, England), 2020, 56, 5681-5684
7126364 CIFC45 H53 B2 N5P -110.776; 12.867; 15.077
99.007; 108.967; 90.735		1948.1Prieschl, Dominic; Arrowsmith, Merle; Dietz, Maximilian; Rempel, Anna; Müller, Marcel; Braunschweig, Holger
Synthesis of polyheterocyclic 1,1-diboryltriazenes by γ-nitrogen insertion of azides into activated B-B single bonds.
Chemical communications (Cambridge, England), 2020, 56, 5681-5684
7126365 CIFC52 H58 B2 F3 N4.87P -110.5695; 15.3466; 16.2221
65.195; 87.805; 72.0887		2260.22Prieschl, Dominic; Arrowsmith, Merle; Dietz, Maximilian; Rempel, Anna; Müller, Marcel; Braunschweig, Holger
Synthesis of polyheterocyclic 1,1-diboryltriazenes by γ-nitrogen insertion of azides into activated B-B single bonds.
Chemical communications (Cambridge, England), 2020, 56, 5681-5684
7126366 CIFC53 H64 B2 N6P -113.097; 14.799; 14.975
63.842; 85.29; 64.034		2320Prieschl, Dominic; Arrowsmith, Merle; Dietz, Maximilian; Rempel, Anna; Müller, Marcel; Braunschweig, Holger
Synthesis of polyheterocyclic 1,1-diboryltriazenes by γ-nitrogen insertion of azides into activated B-B single bonds.
Chemical communications (Cambridge, England), 2020, 56, 5681-5684
7126367 CIFC47 H58 B2 N4P -18.538; 11.12; 21.468
98.92; 91.29; 96.808		1997.6Prieschl, Dominic; Arrowsmith, Merle; Dietz, Maximilian; Rempel, Anna; Müller, Marcel; Braunschweig, Holger
Synthesis of polyheterocyclic 1,1-diboryltriazenes by γ-nitrogen insertion of azides into activated B-B single bonds.
Chemical communications (Cambridge, England), 2020, 56, 5681-5684
7126368 CIFC50 H60 Au6 F12 N8 O2 P2 S4F d d d :212.36; 29.522; 35.0152
90; 90; 90		12777Salorinne, Kirsi; Man, Renee W. Y.; Lummis, Paul A.; Hazer, Maryam Sabooni Asre; Malola, Sami; Yim, Jacky C.-H.; Veinot, Alex J.; Zhou, Wenxia; Häkkinen, Hannu; Nambo, Masakazu; Crudden, Cathleen M.
Synthesis and properties of an Au<sub>6</sub> cluster supported by a mixed N-heterocyclic carbene-thiolate ligand.
Chemical communications (Cambridge, England), 2020, 56, 6102-6105
7126369 CIFC14 H18 Au Br N2 O SP -19.2685; 9.2937; 10.4915
66.938; 78.837; 79.362		809.82Salorinne, Kirsi; Man, Renee W. Y.; Lummis, Paul A.; Hazer, Maryam Sabooni Asre; Malola, Sami; Yim, Jacky C.-H.; Veinot, Alex J.; Zhou, Wenxia; Häkkinen, Hannu; Nambo, Masakazu; Crudden, Cathleen M.
Synthesis and properties of an Au<sub>6</sub> cluster supported by a mixed N-heterocyclic carbene-thiolate ligand.
Chemical communications (Cambridge, England), 2020, 56, 6102-6105
7126370 CIFC20 H23 B O2C 1 2/c 125.557; 5.612; 25.398
90; 113.817; 90		3333Maza, Ricardo J.; Royes, Jordi; Carbó, Jorge J; Fernández, Elena
Consecutive borylcupration/C-C coupling of γ-alkenyl aldehydes towards diastereoselective 2-(borylmethyl)cycloalkanols.
Chemical communications (Cambridge, England), 2020, 56, 5973-5976
7126371 CIFC26 H35 B O3P 1 21/c 117.9052; 6.4987; 19.8249
90; 100.138; 90		2270.8Maza, Ricardo J.; Royes, Jordi; Carbó, Jorge J; Fernández, Elena
Consecutive borylcupration/C-C coupling of γ-alkenyl aldehydes towards diastereoselective 2-(borylmethyl)cycloalkanols.
Chemical communications (Cambridge, England), 2020, 56, 5973-5976
7126372 CIFC169 H128 Ce20 Cl16 N3 O62P 1 21 120.314; 24.463; 28.508
90; 91.975; 90		14158Russell-Webster, Bradley; Abboud, Khalil A.; Christou, George
Molecular nanoparticles of cerium dioxide: structure-directing effect of halide ions.
Chemical communications (Cambridge, England), 2020, 56, 5382-5385
7126373 CIFC48 H38 Ce3 F0.5 N1.5 O15.5P -114.683; 14.726; 14.909
60.518; 65.035; 62.487		2408Russell-Webster, Bradley; Abboud, Khalil A.; Christou, George
Molecular nanoparticles of cerium dioxide: structure-directing effect of halide ions.
Chemical communications (Cambridge, England), 2020, 56, 5382-5385
7126374 CIFC21 H23 N3 O5P -16.9699; 10.2021; 14.9823
72.265; 77.347; 82.211		987.37Bashir, Muhammad Adnan; Zuo, Honghua; Lu, Xunbo; Wu, Yuzhou; Zhong, Fangrui
Harnessing structurally unbiased ortho-benzoquinone monoimine for biomimetic oxidative [4+2] cycloaddition with enamines.
Chemical communications (Cambridge, England), 2020, 56, 5965-5968
7126375 CIFC89 H70 Cl8 F6 N8 Ni4 O6 PP -114.2332; 16.4798; 19.285
112.704; 92.701; 103.281		4014.6Jacob, Samuel I.; Douair, Iskander; Wu, Guang; Maron, Laurent; Ménard, Gabriel
A tetranuclear nickel cluster isolated in multiple high-valent states.
Chemical communications (Cambridge, England), 2020, 56, 8182-8185
7126376 CIFC41 H30 N4 Ni2 O3P -113.084; 15.98; 22.737
107.838; 105.17; 95.623		4285Jacob, Samuel I.; Douair, Iskander; Wu, Guang; Maron, Laurent; Ménard, Gabriel
A tetranuclear nickel cluster isolated in multiple high-valent states.
Chemical communications (Cambridge, England), 2020, 56, 8182-8185
7126377 CIFC71.5 H30 B Cl3 F20 N4 Ni2 O3P -117.673; 19; 19.53
87.662; 78.355; 89.016		6417Jacob, Samuel I.; Douair, Iskander; Wu, Guang; Maron, Laurent; Ménard, Gabriel
A tetranuclear nickel cluster isolated in multiple high-valent states.
Chemical communications (Cambridge, England), 2020, 56, 8182-8185
7126378 CIFC184 H72 B4 Cl12 F80 N8 Ni4 O6P 1 2/n 117.902; 28.102; 19.0679
90; 90.382; 90		9592.5Jacob, Samuel I.; Douair, Iskander; Wu, Guang; Maron, Laurent; Ménard, Gabriel
A tetranuclear nickel cluster isolated in multiple high-valent states.
Chemical communications (Cambridge, England), 2020, 56, 8182-8185
7126379 CIFC20 H18 N2 O5P -110.0493; 12.6674; 14.606
79.358; 80.034; 89.938		1798.9O'Malley, Ciarán; Erxleben, Andrea; Kellehan, Seamus; McArdle, Patrick
Unprecedented morphology control of gas phase cocrystal growth using multi zone heating and tailor made additives.
Chemical communications (Cambridge, England), 2020, 56, 5657-5660
7126380 CIFC64 H44 F8 N4 O14P 1 21/c 127.197; 3.7093; 26.924
90; 94.626; 90		2707.3O'Malley, Ciarán; Erxleben, Andrea; Kellehan, Seamus; McArdle, Patrick
Unprecedented morphology control of gas phase cocrystal growth using multi zone heating and tailor made additives.
Chemical communications (Cambridge, England), 2020, 56, 5657-5660
7126381 CIFC19 H13 F2 N O3P 1 21/c 13.8999; 34.7661; 11.4896
90; 94.404; 90		1553.21O'Malley, Ciarán; Erxleben, Andrea; Kellehan, Seamus; McArdle, Patrick
Unprecedented morphology control of gas phase cocrystal growth using multi zone heating and tailor made additives.
Chemical communications (Cambridge, England), 2020, 56, 5657-5660
7126382 CIFC36 H24 F4 N2 O6P 1 21/n 13.7762; 29.2094; 13.5261
90; 96.309; 90		1482.9O'Malley, Ciarán; Erxleben, Andrea; Kellehan, Seamus; McArdle, Patrick
Unprecedented morphology control of gas phase cocrystal growth using multi zone heating and tailor made additives.
Chemical communications (Cambridge, England), 2020, 56, 5657-5660
7126383 CIFC108 H123 Al4 Cl3 Dy2 F72 N2 O8P 1 21/c 113.8684; 30.4814; 16.1283
90; 97.72; 90		6756.1Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126384 CIFC26 H44 Li O YP 1 21/n 19.253; 15.4572; 18.3771
90; 94.016; 90		2621.9Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126385 CIFC108 H123 Al4 Cl3 Dy0.2 F72 N2 O8 Y1.8P 1 21/c 114.14639; 30.4739; 16.04187
90; 98.2178; 90		6844.57Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126386 CIFC108 H123 Al4 Cl3 F72 N2 O8 Y2P 1 21/c 114.1215; 30.3026; 16.0232
90; 98.421; 90		6782.7Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126387 CIFC76 H116 Al2 Y2P -111.2354; 12.454; 14.8193
103.894; 100.299; 111.86		1783.5Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126388 CIFC76 H116 Al2 Dy2P -111.1938; 12.4457; 14.8073
104.043; 100.205; 111.785		1774.66Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126389 CIFC101 H104 Al B Dy2 F36 O4P 1 21/c 115.5064; 21.8874; 31.229
90; 101.817; 90		10374.3Errulat, Dylan; Gabidullin, Bulat; Mansikkamäki, Akseli; Murugesu, Muralee
Two heads are better than one: improving magnetic relaxation in the dysprosium metallocene upon dimerization by use of an exceptionally weakly-coordinating anion.
Chemical communications (Cambridge, England), 2020, 56, 5937-5940
7126390 CIFC27.5 H31 B Cl F8 N2 P S2P 1 21/c 115.04; 13.437; 16.768
90; 111.168; 90		3160Adachi, Yohei; Arai, Fuka; Jäkle, Frieder
Extended conjugated borenium dimers via late stage functionalization of air-stable borepinium ions.
Chemical communications (Cambridge, England), 2020, 56, 5119-5122
7126391 CIFC20 H20 N2 O3C 1 2/c 111.906; 21.361; 13.77
90; 105.875; 90		3368Babu, Kaki Raveendra; Han, Wendan; Chen, Jian-Bo; Li, Yang; Tang, Yuhai; Zhang, Wenquan; Xu, Wenbo; Xu, Silong
A three-component reaction of phosphorus ylides with isocyanates: facile synthesis of 2-amino-3-carboxylate-4-quinolones.
Chemical communications (Cambridge, England), 2020, 56, 5909-5912
7126392 CIFC20 H20 N2 O3P -18.842; 13.473; 14.699
83.102; 79.47; 89.425		1709Babu, Kaki Raveendra; Han, Wendan; Chen, Jian-Bo; Li, Yang; Tang, Yuhai; Zhang, Wenquan; Xu, Wenbo; Xu, Silong
A three-component reaction of phosphorus ylides with isocyanates: facile synthesis of 2-amino-3-carboxylate-4-quinolones.
Chemical communications (Cambridge, England), 2020, 56, 5909-5912
7126393 CIFC63 H60 N2 O8 P2C 1 2/c 133.89; 9.68; 18.339
90; 115.521; 90		5429Babu, Kaki Raveendra; Han, Wendan; Chen, Jian-Bo; Li, Yang; Tang, Yuhai; Zhang, Wenquan; Xu, Wenbo; Xu, Silong
A three-component reaction of phosphorus ylides with isocyanates: facile synthesis of 2-amino-3-carboxylate-4-quinolones.
Chemical communications (Cambridge, England), 2020, 56, 5909-5912
7126394 CIFC13 H15 N O2 SP 1 21/c 115.037; 5.654; 16.695
90; 116.037; 90		1275.3Babu, Kaki Raveendra; Han, Wendan; Chen, Jian-Bo; Li, Yang; Tang, Yuhai; Zhang, Wenquan; Xu, Wenbo; Xu, Silong
A three-component reaction of phosphorus ylides with isocyanates: facile synthesis of 2-amino-3-carboxylate-4-quinolones.
Chemical communications (Cambridge, England), 2020, 56, 5909-5912
7126395 CIFC66 H82 B Br Mo N6 O5 P2 PtP 1 21/n 122.4595; 12.1952; 24.7641
90; 102.513; 90		6621.73Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126396 CIFC76 H82 B2 Br2 Cl8 Mo2 N12 O4 P2 Pd2P 1 21/n 111.3977; 30.1539; 13.2985
90; 109.428; 90		4310.25Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126397 CIFC54 H52 B Br N6 O2 P2 Pt WP 1 21/n 19.5923; 22.6404; 23.4154
90; 98.636; 90		5027.55Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126398 CIFC44 H46 B Br Mo N6 O2 P2 PdC 1 2/c 142.971; 10.446; 20.5602
90; 94.607; 90		9199.1Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126399 CIFC82 H92 B2 Br2 Mo2 N12 O7 P2 Pd2P 1 21/n 127.0575; 11.7128; 29.6534
90; 104.965; 90		9079Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126400 CIFC82 H99 B2 Br2 Mo2 N12 O6.5 P2 Pt2P 1 21/n 126.9732; 11.6694; 29.657
90; 105.134; 90		9011.1Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126401 CIFC39 H40 B Br Cl9 N6 O2 P Pd WP -111.41; 13.4275; 17.2454
85.274; 87.055; 70.772		2485.43Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126402 CIFC52 H52 B Br N6 O2 P2 Pd WP 1 21/n 121.7995; 12.8236; 22.874
90; 111.409; 90		5953.2Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126403 CIFC48 H58 Au N3P 1 21/n 110.797; 16.6498; 24.697
90; 95.768; 90		4417.2Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126404 CIFC34 H34 Cl2 I NP n a 2118.2744; 10.4465; 17.007
90; 90; 90		3246.7Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126405 CIFC41 H45 Cl3 N2 PdP 1 21/n 18.822; 20.173; 21.011
90; 93.993; 90		3730.2Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126406 CIFC63 H78 Au B2 F8 N5 PdP 1 21/m 115.3922; 14.4465; 16.7191
90; 115.716; 90		3349.5Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126407 CIFC46 H42 Au F3 N O3 P SP 1 21/c 114.4529; 13.4595; 21.5529
90; 93.956; 90		4182.67Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126408 CIFC59 H70 Au Cl2 F3 N O5 P3 Pd SP -113.9859; 14.735; 15.1208
84.537; 82.442; 89.562		3074.99Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126409 CIFC12 H28 Br12 Cu6 N4 PbR -3 :H11.453; 11.453; 22.637
90; 90; 120		2571.5Jing, Chang-Qing; Wu, Jia-Hang; Cao, Yao-Yao; Che, Hang-Xin; Zhao, Xian-Mei; Yue, Meng; Liao, Yuan-Yuan; Yue, Cheng-Yang; Lei, Xiao-Wu
A three-dimensional cuprous lead bromide framework with highly efficient and stable thermochromic luminescence properties.
Chemical communications (Cambridge, England), 2020, 56, 5925-5928
7126410 CIFC13 H14 N2 O2I 1 2/a 116.722; 7.3514; 20.934
90; 102.85; 90		2509Wang, Ya; Zhou, Yao; Song, Qiuling
[3+1+1] type cyclization of ClCF<sub>2</sub>COONa for the assembly of imidazoles and tetrazoles via in situ generated isocyanides.
Chemical communications (Cambridge, England), 2020, 56, 6106-6109
7126411 CIFC8 H8 N4P 1 21/n 19.7747; 5.6834; 14.3307
90; 96.261; 90		791.37Wang, Ya; Zhou, Yao; Song, Qiuling
[3+1+1] type cyclization of ClCF<sub>2</sub>COONa for the assembly of imidazoles and tetrazoles via in situ generated isocyanides.
Chemical communications (Cambridge, England), 2020, 56, 6106-6109
7126412 CIFC14 H16 N2 O2P 1 21/n 18.1279; 8.6652; 18.746
90; 96.939; 90		1310.6Wang, Ya; Zhou, Yao; Song, Qiuling
[3+1+1] type cyclization of ClCF<sub>2</sub>COONa for the assembly of imidazoles and tetrazoles via in situ generated isocyanides.
Chemical communications (Cambridge, England), 2020, 56, 6106-6109
7126413 CIFC53 H46 N4P -111.7669; 12.1939; 15.1362
102.506; 97.611; 102.676		2031.3Li, Kuofei; Zhu, Yunhui; Yao, Bing; Chen, Yuannan; Deng, Hao; Zhang, Qisheng; Zhan, Hongmei; Xie, Zhiyuan; Cheng, Yanxiang
Rotation-restricted thermally activated delayed fluorescence compounds for efficient solution-processed OLEDs with EQEs of up to 24.3% and small roll-off.
Chemical communications (Cambridge, England), 2020, 56, 5957-5960
7126414 CIFC77 H64 N6P 1 21/n 118.369; 16.572; 20.32
90; 99.726; 90		6096.7Li, Kuofei; Zhu, Yunhui; Yao, Bing; Chen, Yuannan; Deng, Hao; Zhang, Qisheng; Zhan, Hongmei; Xie, Zhiyuan; Cheng, Yanxiang
Rotation-restricted thermally activated delayed fluorescence compounds for efficient solution-processed OLEDs with EQEs of up to 24.3% and small roll-off.
Chemical communications (Cambridge, England), 2020, 56, 5957-5960
7126415 CIFC93 H96 N6P -112.351; 18.25; 19.587
101.343; 93.315; 108.024		4082.9Li, Kuofei; Zhu, Yunhui; Yao, Bing; Chen, Yuannan; Deng, Hao; Zhang, Qisheng; Zhan, Hongmei; Xie, Zhiyuan; Cheng, Yanxiang
Rotation-restricted thermally activated delayed fluorescence compounds for efficient solution-processed OLEDs with EQEs of up to 24.3% and small roll-off.
Chemical communications (Cambridge, England), 2020, 56, 5957-5960
7126416 CIFC94 H58 N8 O24 Zn3P 1 21 112.652; 18.915; 21.672
90; 105.25; 90		5004Li, Peng; Sui, Qi; Guo, Meng-Yue; Yang, Shuai-Liang; Bu, Ran; Gao, En-Qing
Selective chemochromic and chemically-induced photochromic response of a metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 5929-5932
7126417 CIFC18 H20 N2 O4P 21 21 2111.5787; 16.5844; 17.9315
90; 90; 90		3443.3Velázquez, Marta; Alberca, Saúl; Iglesias-Sigüenza, Javier; Fernández, Rosario; Lassaletta, José M; Monge, David
Catalytic enantioselective synthesis of α-aryl α-hydrazino esters and amides.
Chemical communications (Cambridge, England), 2020, 56, 5823-5826
7126418 CIFC28 H38 Cl6 N2 PdP 1 21/n 112.8037; 17.1488; 15.3764
90; 104.478; 90		3268.95Guillet, Sébastien G; Voloshkin, Vladislav A.; Saab, Marina; Beliš, Marek; Van Hecke, Kristof; Nahra, Fady; Nolan, Steven P.
Understanding existing and designing novel synthetic routes to Pd-PEPPSI-NHC and Pd-PEPPSI-PR<sub>3</sub> pre-catalysts.
Chemical communications (Cambridge, England), 2020, 56, 5953-5956
7126419 CIFC23 H20 Cl2 N P PdP 1 21/c 18.8655; 10.7674; 22.2732
90; 93.155; 90		2122.94Guillet, Sébastien G; Voloshkin, Vladislav A.; Saab, Marina; Beliš, Marek; Van Hecke, Kristof; Nahra, Fady; Nolan, Steven P.
Understanding existing and designing novel synthetic routes to Pd-PEPPSI-NHC and Pd-PEPPSI-PR<sub>3</sub> pre-catalysts.
Chemical communications (Cambridge, England), 2020, 56, 5953-5956
7126420 CIFC20.5 H29.5 Cl3.5 N3 PdP c c 226.6806; 15.682; 11.6312
90; 90; 90		4866.55Guillet, Sébastien G; Voloshkin, Vladislav A.; Saab, Marina; Beliš, Marek; Van Hecke, Kristof; Nahra, Fady; Nolan, Steven P.
Understanding existing and designing novel synthetic routes to Pd-PEPPSI-NHC and Pd-PEPPSI-PR<sub>3</sub> pre-catalysts.
Chemical communications (Cambridge, England), 2020, 56, 5953-5956
7126421 CIFC14 H13 N O4P -17.1411; 7.8726; 10.6572
102.1; 92.658; 101.463		571.71Fueyo-González, Francisco; Garcia-Fernandez, Emilio; Martínez, David; Infantes, Lourdes; Orte, Angel; González-Vera, Juan A; Herranz, Rosario
Smart lanthanide antennas for sensing water.
Chemical communications (Cambridge, England), 2020, 56, 5484-5487
7126422 CIFC16 H20 N O5 PP 1 21/c 113.804; 13.802; 16.169
90; 90.79; 90		3080.3Fueyo-González, Francisco; Garcia-Fernandez, Emilio; Martínez, David; Infantes, Lourdes; Orte, Angel; González-Vera, Juan A; Herranz, Rosario
Smart lanthanide antennas for sensing water.
Chemical communications (Cambridge, England), 2020, 56, 5484-5487
7126423 CIFC32 H31 Cl3 Eu F9 N2 O21 S3C 1 2/c 127.777; 14.271; 26.502
90; 115.444; 90		9487Fueyo-González, Francisco; Garcia-Fernandez, Emilio; Martínez, David; Infantes, Lourdes; Orte, Angel; González-Vera, Juan A; Herranz, Rosario
Smart lanthanide antennas for sensing water.
Chemical communications (Cambridge, England), 2020, 56, 5484-5487
7126424 CIFC35 H50 Eu F9 N2 O24 P2 S3P 1 21/n 115.919; 13.486; 24.95
90; 105.115; 90		5171Fueyo-González, Francisco; Garcia-Fernandez, Emilio; Martínez, David; Infantes, Lourdes; Orte, Angel; González-Vera, Juan A; Herranz, Rosario
Smart lanthanide antennas for sensing water.
Chemical communications (Cambridge, England), 2020, 56, 5484-5487
7126425 CIFC39 H38 B F2 N3 O5P -111.152; 12.967; 13.78
113.934; 105.531; 98.396		1679.9Ou, Changjin; Zhang, Yewei; Ge, Wei; Zhong, Liping; Huang, Yong; Si, Weili; Wang, Wenjun; Zhao, Yongxiang; Dong, Xiaochen
A three-dimensional BODIPY-iron(iii) compound with improved H<sub>2</sub>O<sub>2</sub>-response for NIR-II photoacoustic imaging guided chemodynamic/photothermal therapy.
Chemical communications (Cambridge, England), 2020, 56, 6281-6284
7126426 CIFC64 H54 Fe3 N12 O2P 1 21/n 111.719; 22.281; 20.337
90; 91.485; 90		5308Hyun, Sung-Min; Upadhyay, Apoorva; Das, Anuvab; Burns, Corey P.; Sung, Siyoung; Beaty, Jeremy D.; Bhuvanesh, Nattamai; Nippe, Michael; Powers, David C.
Kinetic versus thermodynamic metalation enables synthesis of isostructural homo- and heterometallic trinuclear clusters.
Chemical communications (Cambridge, England), 2020, 56, 5893-5896
7126427 CIFC64 H54.36 N12 O2.18 Zn3P 1 21/n 111.5922; 22.523; 20.5743
90; 92.1491; 90		5368Hyun, Sung-Min; Upadhyay, Apoorva; Das, Anuvab; Burns, Corey P.; Sung, Siyoung; Beaty, Jeremy D.; Bhuvanesh, Nattamai; Nippe, Michael; Powers, David C.
Kinetic versus thermodynamic metalation enables synthesis of isostructural homo- and heterometallic trinuclear clusters.
Chemical communications (Cambridge, England), 2020, 56, 5893-5896
7126428 CIFC64 H54 Fe2 N12 O2 ZnP 1 21/n 111.664; 22.4568; 20.4213
90; 91.781; 90		5346.5Hyun, Sung-Min; Upadhyay, Apoorva; Das, Anuvab; Burns, Corey P.; Sung, Siyoung; Beaty, Jeremy D.; Bhuvanesh, Nattamai; Nippe, Michael; Powers, David C.
Kinetic versus thermodynamic metalation enables synthesis of isostructural homo- and heterometallic trinuclear clusters.
Chemical communications (Cambridge, England), 2020, 56, 5893-5896
7126429 CIFC19.99 H28.37 K1.15 Mn3.25 Na O15.73C 1 2/c 124.928; 24.515; 25.527
90; 112.915; 90		14369Liu, Shuai; Deng, Youmei; Xu, Feng
An inorganic-organic hybrid Mn<sup>III</sup>{Mn}<sub>2</sub> cluster consisting of rare Lindqvist-like Mn<sub>6</sub> subunits with high proton conductivity.
Chemical communications (Cambridge, England), 2020, 56, 6066-6069
7126430 CIFC44 H34 OP 1 21/n 18.0514; 29.7733; 12.8449
90; 92.127; 90		3077.02Mori, Sakura; Akita, Motoko; Suzuki, Shuichi; Asano, Motoko S.; Murata, Michihisa; Akiyama, Tsuyoshi; Matsumoto, Taisuke; Kitamura, Chitoshi; Kato, Shin-Ichiro
Open-shell singlet diradicaloid difluoreno[4,3-b:3',4'-d]furan and its radical cation and dianion.
Chemical communications (Cambridge, England), 2020, 56, 5881-5884
7126431 CIFB Ba6 Cl9 O3P 1 21/n 18.229; 12.2589; 19.08
90; 90.203; 90		1924.7Li, Wei; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng
Ba<sub>6</sub>BO<sub>3</sub>Cl<sub>9</sub> and Pb<sub>6</sub>BO<sub>4</sub>Cl<sub>7</sub>: structural insights into ortho-borates with uncondensed BO<sub>4</sub> tetrahedra.
Chemical communications (Cambridge, England), 2020, 56, 6086-6089
7126432 CIFB Cl7 O4 Pb6P -18.001; 8.054; 13.116
89.522; 89.663; 69.942		793.9Li, Wei; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng
Ba<sub>6</sub>BO<sub>3</sub>Cl<sub>9</sub> and Pb<sub>6</sub>BO<sub>4</sub>Cl<sub>7</sub>: structural insights into ortho-borates with uncondensed BO<sub>4</sub> tetrahedra.
Chemical communications (Cambridge, England), 2020, 56, 6086-6089
7126433 CIFC24 H29 B F2 O3P -110.1095; 14.6951; 16.0516
70.598; 79.739; 77.184		2178.99Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126434 CIFC24 H29 B F2 O3P -18.4132; 9.9177; 15.6851
74.475; 86.897; 66.845		1157.49Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126435 CIFC24 H29 B F2 O3P -18.5049; 9.9575; 15.6872
74.405; 86.917; 66.543		1171.72Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126436 CIFC24 H29 B F2 O3P -110.1447; 15.1024; 16.1256
70.107; 78.921; 78.57		2256.1Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126437 CIFC17 H15 B F2 O3P 1 21/c 17.6754; 19.1327; 10.149
90; 102.782; 90		1453.46Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126438 CIFC24 H29 B F2 O3P -110.1293; 14.9169; 16.0997
70.326; 79.384; 77.847		2222.2Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126439 CIFC24 H29 B F2 O3P -110.1217; 14.766; 16.0705
70.555; 79.713; 77.319		2195.03Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126440 CIFC24 H29 B F2 O3P -110.1611; 15.2065; 16.1543
70.258; 78.911; 79.039		2284.2Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126441 CIFC20 H21 B F2 O3P b c a7.1609; 10.0337; 48.7164
90; 90; 90		3500.29Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126442 CIFC17 H15 B F2 O3P 1 21/c 17.9445; 19.2382; 10.3606
90; 104.183; 90		1535.2Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126443 CIFC17 H15 B F2 O3P 1 21/c 17.8494; 19.191; 10.3146
90; 103.76; 90		1509.18Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126444 CIFC17 H15 B F2 O3P 1 21/c 17.7481; 19.1442; 10.2334
90; 103.133; 90		1478.23Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126445 CIFC20 H21 B F2 O3P b c a7.1936; 10.205; 50.76
90; 90; 90		3726Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126446 CIFC20 H21 B F2 O3P b c a7.2099; 10.1738; 49.415
90; 90; 90		3624.7Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126447 CIFC20 H21 B F2 O3P b c a7.175; 10.0917; 49.0041
90; 90; 90		3548.29Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126448 CIFC31 H38 N4 O5P 21 21 2110.1246; 16.0039; 18.3736
90; 90; 90		2977.13Wang, Donglei; Jiang, Qianwen; Yang, Xiaoyu
Atroposelective synthesis of configurationally stable nonbiaryl N-C atropisomers through direct asymmetric aminations of 1,3-benzenediamines.
Chemical communications (Cambridge, England), 2020, 56, 6201-6204
7126449 CIFC8 H12 Cl2 Cu N5 O0.5P -17.7357; 12.816; 13.522
110.78; 103.66; 96.17		1190.6Schäfer, Dominic; Fink, Fabian; Kleinschmidt, Denise; Keisers, Kristina; Thomas, Fabian; Hoffmann, Alexander; Pich, Andrij; Herres-Pawlis, Sonja
Enhanced catalytic activity of copper complexes in microgels for aerobic oxidation of benzyl alcohols.
Chemical communications (Cambridge, England), 2020, 56, 5601-5604
7126450 CIFC23 H16 B F10 N SP 1 21 110.5637; 7.3903; 13.8954
90; 98.8924; 90		1071.76Fischer, Malte; Schmidtmann, Marc
B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>- and HB(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>-mediated transformations of isothiocyanates.
Chemical communications (Cambridge, England), 2020, 56, 6205-6208
7126451 CIFC16 H20 O8 Zn2P n a 2117.8332; 9.0061; 13.2032
90; 90; 90		2120.53Zhang, Jiajia; Cui, Fang; Li, Li; Liu, Yang; Zhang, Xiao; Cui, Tieyu
From coordination polymers to nanocrystals: general and facile synthesis of ultra-small metal oxide nanocrystals.
Chemical communications (Cambridge, England), 2020, 56, 6145-6148
7126452 CIFC14 H5 N3 O5P 1 21/c 15.0814; 6.9825; 17.0804
90; 93.994; 90		604.56Niazi, Muhammad Rizwan; Hamzehpoor, Ehsan; Ghamari, Pegah; Perepichka, Igor F.; Perepichka, Dmitrii F.
Nitroaromatics as n-type organic semiconductors for field effect transistors.
Chemical communications (Cambridge, England), 2020, 56, 6432-6435
7126453 CIFC14 H10 Cu N2 O3P 1 21/n 16.4066; 18.6435; 9.8389
90; 96.696; 90		1167.16Khanra, Somnath; Ta, Sabyasachi; Paladhi, Ankush; Ghosh, Milan; Ghosh, Subhasis; Hira, Sumit Kumar; Manna, Partha Partim; Brandão, Paula; Félix, Vítor; Das, Debasis
A polynuclear Cu(ii) complex for real time monitoring of mitochondrial cytochrome C release during cellular apoptosis.
Chemical communications (Cambridge, England), 2020, 56, 6563-6566
7126454 CIFC52 H48 B F24 N2 Na O7P 1 21/c 112.7633; 18.502; 24.5224
90; 96.5057; 90		5753.6Iniesta, Ester; Vidal-Ferran, Anton
Supramolecularly regulated copper-bisoxazoline catalysts for the efficient insertion of carbenoid species into hydroxyl bonds.
Chemical communications (Cambridge, England), 2020, 56, 6364-6367
7126455 CIFC44 H82 Cl0 Cu2 F24 N4 Na2 O15 P4P 1 21/n 110.5906; 25.0689; 12.4435
90; 92.9669; 90		3299.3Iniesta, Ester; Vidal-Ferran, Anton
Supramolecularly regulated copper-bisoxazoline catalysts for the efficient insertion of carbenoid species into hydroxyl bonds.
Chemical communications (Cambridge, England), 2020, 56, 6364-6367
7126456 CIFC24 H44 Cu F12 N2 Na O9 P2P -111.243; 12.5262; 14.6345
64.708; 87.283; 73.184		1776.8Iniesta, Ester; Vidal-Ferran, Anton
Supramolecularly regulated copper-bisoxazoline catalysts for the efficient insertion of carbenoid species into hydroxyl bonds.
Chemical communications (Cambridge, England), 2020, 56, 6364-6367
7126457 CIFC15 H14 F3 N O2 SC 1 2/c 125.516; 5.6738; 21.937
90; 110.176; 90		2981Zeng, Hao; Zhu, Chuanle; Liu, Chi; Cai, Yingying; Chen, Fulin; Jiang, Huanfeng
Three component hydroxyletherification and hydroxylazidation of (trifluoromethyl)alkenes: access to α-trifluoromethyl β-heteroatom substituted tertiary alcohols.
Chemical communications (Cambridge, England), 2020, 56, 6241-6244
7126458 CIFC6 H11 F O4P 1 21 18.1522; 4.739; 9.7711
90; 99.908; 90		371.86Valverde, Pablo; Vendeville, Jean-Baptiste; Hollingsworth, Kristian; Mattey, Ashley P.; Keenan, Tessa; Chidwick, Harriet; Ledru, Helene; Huonnic, Kler; Huang, Kun; Light, Mark E.; Turner, Nicholas; Jiménez-Barbero, Jesús; Galan, M. Carmen; Fascione, Martin A.; Flitsch, Sabine; Turnbull, W. Bruce; Linclau, Bruno
Chemoenzymatic synthesis of 3-deoxy-3-fluoro-l-fucose and its enzymatic incorporation into glycoconjugates.
Chemical communications (Cambridge, England), 2020, 56, 6408-6411
7126459 CIFC77 H118 Al2 N6 O2C 1 2/c 123.926; 13.52; 47.134
90; 98.006; 90		15098Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126460 CIFC70 H108 Al2 N8P -111.946; 14.183; 21.699
71.614; 88.934; 76.753		3390.2Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126461 CIFC85.5 H128 Al2 N8P -112.9012; 15.4561; 22.3126
100.431; 95.38; 110.218		4046.7Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126462 CIFC215 H318 Al4 N16 Na2 O4P -113.092; 17.852; 21.332
90.53; 90.05; 96.922		4949Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126463 CIFC37 H59 Al N4P 4112.7376; 12.7376; 22.3806
90; 90; 90		3631.2Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126464 CIFC53 H75 Al N4P c a 2120.25; 12.5817; 18.94
90; 90; 90		4825.5Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126465 CIFC17 H13 I O4P -19.5534; 9.6302; 10.2451
74.922; 85.722; 61.931		801.8Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126466 CIFC18 H14 F I O4P 21 21 218.7643; 9.1745; 20.1935
90; 90; 90		1623.72Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126467 CIFC19 H15 I O4P 1 21/n 18.0931; 13.1306; 15.5266
90; 95.488; 90		1642.41Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126468 CIFC19 H17 I O5P -19.8357; 10.4353; 10.4634
111.642; 106.312; 106.245		865.1Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126469 CIFC19 H14 F3 I O4C 1 c 19.2645; 22.2327; 18.2492
90; 101.504; 90		3683.36Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126470 CIFC19 H17 I O4P 1 21/n 110.5655; 14.926; 11.4963
90; 107.437; 90		1729.66Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126471 CIFC24 H40 Cl2 Cu2 N2 O3 P2P n a 2117.8896; 11.8315; 14.1427
90; 90; 90		2993.46Scheerder, Arthur R.; Lutz, Martin; Broere, Daniël L J
Unexpected reactivity of a PONNOP 'expanded pincer' ligand.
Chemical communications (Cambridge, England), 2020, 56, 8198-8201
7126472 CIFC16 H38 Cl2 Ni O2 P2P -17.8506; 8.205; 9.6512
111.818; 100.304; 97.698		554Scheerder, Arthur R.; Lutz, Martin; Broere, Daniël L J
Unexpected reactivity of a PONNOP 'expanded pincer' ligand.
Chemical communications (Cambridge, England), 2020, 56, 8198-8201
7126473 CIFC26 H44 Br2 N2 Ni O3.5 P2P -18.2836; 11.8373; 16.2323
93.988; 96.686; 93.178		1573.77Scheerder, Arthur R.; Lutz, Martin; Broere, Daniël L J
Unexpected reactivity of a PONNOP 'expanded pincer' ligand.
Chemical communications (Cambridge, England), 2020, 56, 8198-8201
7126474 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.8059; 5.8059; 13.905
90; 90; 90		468.72Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126475 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.6443; 5.6443; 13.507
90; 90; 90		430.31Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126476 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.7051; 5.7051; 13.6603
90; 90; 90		444.62Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126477 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.6753; 5.6753; 13.593
90; 90; 90		437.82Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126478 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.5997; 5.5997; 13.351
90; 90; 90		418.64Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126479 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.758; 5.758; 13.794
90; 90; 90		457.33Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126480 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.7382; 5.7382; 13.747
90; 90; 90		452.65Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126481 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.5308; 5.5308; 13.126
90; 90; 90		401.5Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126482 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.5604; 5.5604; 13.245
90; 90; 90		409.51Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126483 CIFC78 H54 Cd3 N4 O14P -116.32; 16.974; 19.292
88.171; 70.164; 62.671		4417Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126484 CIFC89 H73 Cd3 Cl3 N6 O14P -116.4; 16.98; 20.488
92.38; 111.486; 116.958		4581.4Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126485 CIFC81.1 H58.4 Cd3 Cl3 N4.5 O13.7P -116.36; 17.031; 19.943
89.551; 69.596; 62.889		4559Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126486 CIFC69 H49 Cd3 N3 O14P -116.754; 16.894; 18.001
66.663; 77.37; 62.283		4137.7Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126487 CIFC83.5 H62.1 Cd3 N5.1 O13.5P -116.377; 17.024; 20.123
90.241; 110.656; 117.102		4580.7Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126488 CIFC94 H83 Cd3 Cl3 N7 O15P -116.459; 17.028; 20.704
92.164; 111.745; 117.015		4650Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126489 CIFC69.75 H50.75 Cd3 N3.25 O14.25P -116.713; 16.927; 17.944
65.931; 77.105; 62.489		4107.1Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126490 CIFC6 H36 Cl6 Cu12 N6 S6P m -3 m12.3881; 12.3881; 12.3881
90; 90; 90		1901.14Hu, Lanxia; Zheng, Aiping; Kang, Yao; Wen, Tian; Zhang, Jian
A supersalt-type copper(i)-thiolate cluster with applications for mechano/thermochromism and the oxygen evolution reaction.
Chemical communications (Cambridge, England), 2020, 56, 3967-3970
7126491 CIFC128 H96 N16 O16C 1 c 122.05; 10.76; 9.34
90; 101.29; 90		2173.1Levine, Andrew M.; Bu, Guanhong; Biswas, Sankarsan; Tsai, Esther H. R.; Braunschweig, Adam B.; Nannenga, Brent L.
Crystal structure and orientation of organic semiconductor thin films by microcrystal electron diffraction and grazing-incidence wide-angle X-ray scattering.
Chemical communications (Cambridge, England), 2020, 56, 4204-4207
7126492 CIFC32 H8 N8 O8 S0P 1 21/c 18.09; 6.39; 11.63
90; 104.71; 90		581.5Levine, Andrew M.; Bu, Guanhong; Biswas, Sankarsan; Tsai, Esther H. R.; Braunschweig, Adam B.; Nannenga, Brent L.
Crystal structure and orientation of organic semiconductor thin films by microcrystal electron diffraction and grazing-incidence wide-angle X-ray scattering.
Chemical communications (Cambridge, England), 2020, 56, 4204-4207
7126493 CIFC432 H560 N64 O60 S16P 1 21/n 115.09; 19.55; 34.77
90; 94.63; 90		10224Levine, Andrew M.; Bu, Guanhong; Biswas, Sankarsan; Tsai, Esther H. R.; Braunschweig, Adam B.; Nannenga, Brent L.
Crystal structure and orientation of organic semiconductor thin films by microcrystal electron diffraction and grazing-incidence wide-angle X-ray scattering.
Chemical communications (Cambridge, England), 2020, 56, 4204-4207
7126494 CIFC19 H24.04 F3 O6 SP -19.3575; 10.2713; 11.5278
94.471; 104.322; 108.484		1003.31Cheng, Ruixiang; Xiong, Wenfang; Qi, Chaorong; Wang, Lu; Ren, Yanwei; Jiang, Huanfeng
Macrocyclization of 3-triflyloxybenzynes with tetrahydrofuran via an anionic thia-Fries rearrangement.
Chemical communications (Cambridge, England), 2020, 56, 6495-6498
7126495 CIFC4 H2 F3 N3 O4 SP 1 21/c 112.0715; 5.7257; 12.5111
90; 101.199; 90		848.27Zhang, Wei; Lin, Jin-Hong; Zhang, Pengfei; Xiao, Ji-Chang
A convenient reagent for the conversion of aldoximes into nitriles and isonitriles.
Chemical communications (Cambridge, England), 2020, 56, 6221-6224
7126496 CIFC14 H30 Cl4 Fe N4 O4P c a 2112.504; 12.83; 13.185
90; 90; 90		2115.2Hay, Moya A.; Sarkar, Arup; Craig, Gavin A.; Marriott, Katie E. R.; Wilson, Claire; Rajaraman, Gopalan; Murrie, Mark
A large axial magnetic anisotropy in trigonal bipyramidal Fe(ii).
Chemical communications (Cambridge, England), 2020, 56, 6826-6829
7126497 CIFC63 H47 N5 O22P -113.7033; 14.2585; 15.6635
104.701; 100.957; 99.729		2829.3Yelgaonkar, Shweta P.; Kiani, Daniyal; Baltrusaitis, Jonas; MacGillivray, Leonard R.
Superstructural diversity in salt-cocrystals: higher-order hydrogen-bonded assemblies formed using U-shaped dications and with assistance of π<sup>-</sup>-π stacking.
Chemical communications (Cambridge, England), 2020, 56, 6708-6710
7126498 CIFC64 H38 N2 O16P -18.8579; 15.7231; 20.017
110.471; 93.635; 106.238		2467Yelgaonkar, Shweta P.; Kiani, Daniyal; Baltrusaitis, Jonas; MacGillivray, Leonard R.
Superstructural diversity in salt-cocrystals: higher-order hydrogen-bonded assemblies formed using U-shaped dications and with assistance of π<sup>-</sup>-π stacking.
Chemical communications (Cambridge, England), 2020, 56, 6708-6710
7126499 CIFC64 H42 N2 O16P 1 21/c 18.4167; 28.6453; 20.8697
90; 100.155; 90		4952.8Yelgaonkar, Shweta P.; Kiani, Daniyal; Baltrusaitis, Jonas; MacGillivray, Leonard R.
Superstructural diversity in salt-cocrystals: higher-order hydrogen-bonded assemblies formed using U-shaped dications and with assistance of π<sup>-</sup>-π stacking.
Chemical communications (Cambridge, England), 2020, 56, 6708-6710
7126500 CIFC9.6 H7.2 F0.8 N1.6 O2.4P n a 2113.7895; 20.62; 3.8818
90; 90; 90		1103.7Sasmal, Sheuli; Sinha, Soumya Kumar; Lahiri, Goutam Kumar; Maiti, Debabrata
A directing group-assisted ruthenium-catalyzed approach to access meta-nitrated phenols.
Chemical communications (Cambridge, England), 2020, 56, 7100-7103
7126501 CIFC5.33 H4.44 N0.89 O1.78P 1 21/c 18.531; 11.1285; 12.0481
90; 110.333; 90		1072.54Sasmal, Sheuli; Sinha, Soumya Kumar; Lahiri, Goutam Kumar; Maiti, Debabrata
A directing group-assisted ruthenium-catalyzed approach to access meta-nitrated phenols.
Chemical communications (Cambridge, England), 2020, 56, 7100-7103
7126502 CIFC84 H48 N12 O38 Th6F m -3 m30.4822; 30.4822; 30.4822
90; 90; 90		28323Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126503 CIFC60 H36 O38 Th6F m -3 m25.052; 25.052; 25.052
90; 90; 90		15722.7Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126504 CIFC42 H24 O19 Th3F m -3 m27.9387; 27.9387; 27.9387
90; 90; 90		21808.1Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126505 CIFC24 H12 O19 Th3F m -3 m21.9026; 21.9026; 21.9026
90; 90; 90		10507.2Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126506 CIFC144 H96 O76 Th12F m -3 m28.2063; 28.2063; 28.2063
90; 90; 90		22440.8Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126507 CIFC399.36 H249.6 O155.84 Th24F m -3 m30.976; 30.976; 30.976
90; 90; 90		29722Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126508 CIFC48 H24 O94 Th12F m -3 m19.0604; 19.0604; 19.0604
90; 90; 90		6924.6Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126509 CIFC26 H32 La1.11 N4.67 O14.17R 3 2 :H16.2731; 16.2731; 66.968
90; 90; 120		15358.1Wang, Shanshan; Li, Shuning; Xiong, Junyu; Lin, Zhengguo; Wei, Wei; Xu, Yanqing
Near-infrared photothermal conversion of stable radicals photoinduced from a viologen-based coordination polymer.
Chemical communications (Cambridge, England), 2020, 56, 7399-7402
7126510 CIFC25 H22 Cl F3 N4P 1 21 15.6933; 12.7845; 15.7666
90; 99.16; 90		1132.95Stewart, Hannah L.; Hanby, Abigail R.; King, Thomas A.; Bond, Andrew D.; Moss, Thomas A.; Sore, Hannah F.; Spring, David R.
An efficient, stereocontrolled and versatile synthetic route to bicyclic partially saturated privileged scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 6818-6821
7126511 CIFC32 H22 As2 N4 O2P -18.366; 8.971; 9.981
70.613; 73.295; 74.157		663.6Fujii, Toshiki; Tanaka, Susumu; Hayashi, Shotaro; Imoto, Hiroaki; Naka, Kensuke
Dipyridinoarsole: a new class of stable and modifiable heteroatom-bridged bipyridines.
Chemical communications (Cambridge, England), 2020, 56, 6035-6038
7126512 CIFC16 H11 N2 PP 1 21/c 113.597; 11.204; 8.645
90; 103.655; 90		1279.8Fujii, Toshiki; Tanaka, Susumu; Hayashi, Shotaro; Imoto, Hiroaki; Naka, Kensuke
Dipyridinoarsole: a new class of stable and modifiable heteroatom-bridged bipyridines.
Chemical communications (Cambridge, England), 2020, 56, 6035-6038
7126513 CIFC16 H11 As N2P 1 21/c 113.672; 11.334; 8.756
90; 104.051; 90		1316.2Fujii, Toshiki; Tanaka, Susumu; Hayashi, Shotaro; Imoto, Hiroaki; Naka, Kensuke
Dipyridinoarsole: a new class of stable and modifiable heteroatom-bridged bipyridines.
Chemical communications (Cambridge, England), 2020, 56, 6035-6038
7126514 CIFC16 H11 N2 O PP -17.692; 9.588; 10.081
88.33; 72.47; 67.903		653.9Fujii, Toshiki; Tanaka, Susumu; Hayashi, Shotaro; Imoto, Hiroaki; Naka, Kensuke
Dipyridinoarsole: a new class of stable and modifiable heteroatom-bridged bipyridines.
Chemical communications (Cambridge, England), 2020, 56, 6035-6038
7126515 CIFC17 H13 As Au Cl3 N2F d d 216.402; 47.39; 9.844
90; 90; 90		7652Fujii, Toshiki; Tanaka, Susumu; Hayashi, Shotaro; Imoto, Hiroaki; Naka, Kensuke
Dipyridinoarsole: a new class of stable and modifiable heteroatom-bridged bipyridines.
Chemical communications (Cambridge, England), 2020, 56, 6035-6038
7126516 CIFC99 H186 Cu2 Ge18 K4 N11 O27P -115.32218; 19.01622; 25.9169
100.068; 101.739; 105.504		6911Wang, Zi-Chuan; Tkachenko, Nikolay V.; Qiao, Lei; Matito, Eduard; Muñoz-Castro, Alvaro; Boldyrev, Alexander I.; Sun, Zhong-Ming
All-metal σ-antiaromaticity in dimeric cluster anion {[CuGe<sub>9</sub>Mes]<sub>2</sub>}<sup>4</sup>.
Chemical communications (Cambridge, England), 2020, 56, 6583-6586
7126517 CIFC28 H22 Cl N3 O0.5 SnP 1 21/c 124.7397; 11.8214; 17.2848
90; 105.783; 90		4864.5Chang, Wei-Chieh; Raj, Ankit; Hiramatsu, Hirotsugu; Li, Han-Jung; Ziegler, Micah S.; Lin, Yichen; Huang, Shengcih; Liu, Hsueh-Ju
Linear, mixed-valent homocatenated tri-tin complexes featuring Sn-Sn bonds.
Chemical communications (Cambridge, England), 2020, 56, 6786-6789
7126518 CIFC52 H36 N6 SnC 1 2/c 139.999; 13.8693; 18.718
90; 113.174; 90		9546.1Chang, Wei-Chieh; Raj, Ankit; Hiramatsu, Hirotsugu; Li, Han-Jung; Ziegler, Micah S.; Lin, Yichen; Huang, Shengcih; Liu, Hsueh-Ju
Linear, mixed-valent homocatenated tri-tin complexes featuring Sn-Sn bonds.
Chemical communications (Cambridge, England), 2020, 56, 6786-6789
7126519 CIFC78 H54 Cl N9 Sn3P -114.4606; 15.1842; 19.5168
94.697; 98.687; 92.921		4213.2Chang, Wei-Chieh; Raj, Ankit; Hiramatsu, Hirotsugu; Li, Han-Jung; Ziegler, Micah S.; Lin, Yichen; Huang, Shengcih; Liu, Hsueh-Ju
Linear, mixed-valent homocatenated tri-tin complexes featuring Sn-Sn bonds.
Chemical communications (Cambridge, England), 2020, 56, 6786-6789
7126520 CIFC87 H70 F3 N9 O5 S Sn3P 1 21/c 122.9751; 20.5456; 17.8253
90; 109.175; 90		7947.4Chang, Wei-Chieh; Raj, Ankit; Hiramatsu, Hirotsugu; Li, Han-Jung; Ziegler, Micah S.; Lin, Yichen; Huang, Shengcih; Liu, Hsueh-Ju
Linear, mixed-valent homocatenated tri-tin complexes featuring Sn-Sn bonds.
Chemical communications (Cambridge, England), 2020, 56, 6786-6789
7126521 CIFC62 H36 N6 O10 Sn2 W2P -111.0407; 13.7762; 20.4412
95.079; 98.842; 111.909		2813.9Chang, Wei-Chieh; Raj, Ankit; Hiramatsu, Hirotsugu; Li, Han-Jung; Ziegler, Micah S.; Lin, Yichen; Huang, Shengcih; Liu, Hsueh-Ju
Linear, mixed-valent homocatenated tri-tin complexes featuring Sn-Sn bonds.
Chemical communications (Cambridge, England), 2020, 56, 6786-6789
7126522 CIFC82 H64 F6 N9 O P Sn3P 1 21/c 122.9606; 20.1323; 17.3947
90; 109.571; 90		7576.2Chang, Wei-Chieh; Raj, Ankit; Hiramatsu, Hirotsugu; Li, Han-Jung; Ziegler, Micah S.; Lin, Yichen; Huang, Shengcih; Liu, Hsueh-Ju
Linear, mixed-valent homocatenated tri-tin complexes featuring Sn-Sn bonds.
Chemical communications (Cambridge, England), 2020, 56, 6786-6789
7126523 CIFC48 H70 B Br Li N2 O6P 21 21 2112.9156; 19.1434; 19.379
90; 90; 90		4791.4Cui, Yunshu; Xiang, Libo; Wang, Junyi; Li, Chunlei; Hao, Wei; Ye, Qing
Storage and release of two electrons from an electron-rich carbon-carbon bond: boron mediated reversible coupling of DMAP and 9-azajulolidine.
Chemical communications (Cambridge, England), 2020, 56, 6794-6797
7126524 CIFC86 H100 B2 N8P 1 21/n 117.282; 30.185; 18.933
90; 111.157; 90		9210.8Cui, Yunshu; Xiang, Libo; Wang, Junyi; Li, Chunlei; Hao, Wei; Ye, Qing
Storage and release of two electrons from an electron-rich carbon-carbon bond: boron mediated reversible coupling of DMAP and 9-azajulolidine.
Chemical communications (Cambridge, England), 2020, 56, 6794-6797
7126525 CIFC46 H56 B Br Cl6 N4P -111.7554; 13.4782; 16.2117
80.556; 77.491; 79.442		2444.4Cui, Yunshu; Xiang, Libo; Wang, Junyi; Li, Chunlei; Hao, Wei; Ye, Qing
Storage and release of two electrons from an electron-rich carbon-carbon bond: boron mediated reversible coupling of DMAP and 9-azajulolidine.
Chemical communications (Cambridge, England), 2020, 56, 6794-6797
7126526 CIFC94 H108 B2 N8P -116.5767; 22.881; 24.197
78.233; 71.81; 85.539		8534.9Cui, Yunshu; Xiang, Libo; Wang, Junyi; Li, Chunlei; Hao, Wei; Ye, Qing
Storage and release of two electrons from an electron-rich carbon-carbon bond: boron mediated reversible coupling of DMAP and 9-azajulolidine.
Chemical communications (Cambridge, England), 2020, 56, 6794-6797
7126527 CIFC51 H62 B Br Cl8 N4P 1 21/c 118.7601; 13.8832; 22.628
90; 112.512; 90		5444.4Cui, Yunshu; Xiang, Libo; Wang, Junyi; Li, Chunlei; Hao, Wei; Ye, Qing
Storage and release of two electrons from an electron-rich carbon-carbon bond: boron mediated reversible coupling of DMAP and 9-azajulolidine.
Chemical communications (Cambridge, England), 2020, 56, 6794-6797
7126528 CIFC40 H32 Cl8 N4 NiP 1 21/c 117.4782; 12.6007; 17.9057
90; 98.164; 90		3903.54Liu, Si-Yu; Kawashima, Hiroyuki; Fukui, Norihito; Shinokubo, Hiroshi
A 2-to-2' 18-to-18' doubly linked Ni(ii) norcorrole dimer: an effectively conjugated antiaromatic dyad.
Chemical communications (Cambridge, England), 2020, 56, 6846-6849
7126529 CIFC76 H66 Cl4 N8 Ni2P -112.0197; 15.476; 18.5471
72.164; 77.709; 86.387		3209Liu, Si-Yu; Kawashima, Hiroyuki; Fukui, Norihito; Shinokubo, Hiroshi
A 2-to-2' 18-to-18' doubly linked Ni(ii) norcorrole dimer: an effectively conjugated antiaromatic dyad.
Chemical communications (Cambridge, England), 2020, 56, 6846-6849
7126530 CIFC38 H31 Cl6 N4 NiC 1 2/c 135.3376; 11.9482; 17.8205
90; 102.422; 90		7348Liu, Si-Yu; Kawashima, Hiroyuki; Fukui, Norihito; Shinokubo, Hiroshi
A 2-to-2' 18-to-18' doubly linked Ni(ii) norcorrole dimer: an effectively conjugated antiaromatic dyad.
Chemical communications (Cambridge, England), 2020, 56, 6846-6849
7126531 CIFC31 H23 N O3P 1 21/n 114.9496; 9.5237; 17.43
90; 111.831; 90		2303.64Gao, Yu-Qi; Hou, Yi; Zhu, Liming; Chen, Junhan; Li, Ruoxin; Zhang, Sheng-Yong; He, Yu-Peng; Xie, Weiqing
Visible-light driven synthesis of polycyclic benzo[d][1,3]oxazocine from 2-aminochalcone.
Chemical communications (Cambridge, England), 2020, 56, 6739-6742
7126532 CIFC28 H23 N O2P 1 21/n 110.1842; 20.0153; 10.5231
90; 95.242; 90		2136.1Gao, Yu-Qi; Hou, Yi; Zhu, Liming; Chen, Junhan; Li, Ruoxin; Zhang, Sheng-Yong; He, Yu-Peng; Xie, Weiqing
Visible-light driven synthesis of polycyclic benzo[d][1,3]oxazocine from 2-aminochalcone.
Chemical communications (Cambridge, England), 2020, 56, 6739-6742
7126533 CIFC58 H42 B2 N2 O4P 1 21/c 117.8827; 7.8947; 15.7916
90; 96.353; 90		2215.7Ohtani, Shunsuke; Nakamura, Masashi; Gon, Masayuki; Tanaka, Kazuo; Chujo, Yoshiki
Synthesis of fully-fused bisboron azomethine complexes and their conjugated polymers with solid-state near-infrared emission.
Chemical communications (Cambridge, England), 2020, 56, 6575-6578
7126534 CIFC27 H28 N2 O5P 1 2/c 15.1905; 9.3677; 23.713
90; 94.729; 90		1149.1He, Hui-Zi; Li, Kun; Yu, Kang-Kang; Lu, Pei-Long; Feng, Mei-Lin; Chen, Shan-Yong; Yu, Xiao-Qi
Additive- and column-free synthesis of rigid bis-coumarins as fluorescent dyes for G-quadruplex sensing via disaggregation-induced emission.
Chemical communications (Cambridge, England), 2020, 56, 6870-6873
7126535 CIFC20 H26 O4 SP 21 21 216.4331; 15.335; 19.485
90; 90; 90		1922.2Mando, Morgane; Grellepois, Fabienne; Riguet, Emmanuel
Organocatalytic enantioselective allylic alkylation of α-aryl γ-lactones: an approach to densely functionalized quaternary stereocentres.
Chemical communications (Cambridge, England), 2020, 56, 6640-6643
7126536 CIFC18 H18 N2 OP 21 21 217.5891; 10.7774; 17.9836
90; 90; 90		1470.89Ganesan, Balaji; Govindan, Karthick; Senadi, Gopal Chandru; Kandasamy, Mohanraj; Lin, Wei-Yu
Copper-catalyzed synthesis of aminoquinolines from β-(2-aminophenyl)-α,β-ynones using DMF as dual synthon.
Chemical communications (Cambridge, England), 2020, 56, 6488-6491
7126537 CIFC14 H21 B10 NP 1 21/c 118.8752; 7.25; 13.1539
90; 96.9162; 90		1786.95Chen, Yu; Quan, Yangjian; Xie, Zuowei
Ir-catalyzed selective dehydrogenative cross-coupling of aryls with o-carboranes via a mixed directing-group strategy.
Chemical communications (Cambridge, England), 2020, 56, 7001-7004
7126538 CIFC12 H20 B10 N2P 1 21/c 119.063; 6.8433; 13.5027
90; 92.491; 90		1759.8Chen, Yu; Quan, Yangjian; Xie, Zuowei
Ir-catalyzed selective dehydrogenative cross-coupling of aryls with o-carboranes via a mixed directing-group strategy.
Chemical communications (Cambridge, England), 2020, 56, 7001-7004
7126539 CIFC18 H34 B20 N2P -111.1641; 11.5247; 12.2762
85.6539; 71.2257; 82.6628		1482.2Chen, Yu; Quan, Yangjian; Xie, Zuowei
Ir-catalyzed selective dehydrogenative cross-coupling of aryls with o-carboranes via a mixed directing-group strategy.
Chemical communications (Cambridge, England), 2020, 56, 7001-7004
7126540 CIFC13 H29 B20 NP 1 21/c 112.1083; 15.2069; 13.3711
90; 92.9866; 90		2458.67Chen, Yu; Quan, Yangjian; Xie, Zuowei
Ir-catalyzed selective dehydrogenative cross-coupling of aryls with o-carboranes via a mixed directing-group strategy.
Chemical communications (Cambridge, England), 2020, 56, 7001-7004
7126541 CIFC13 H20 B10 N2P 21 21 2111.3782; 11.4876; 13.5646
90; 90; 90		1773Chen, Yu; Quan, Yangjian; Xie, Zuowei
Ir-catalyzed selective dehydrogenative cross-coupling of aryls with o-carboranes via a mixed directing-group strategy.
Chemical communications (Cambridge, England), 2020, 56, 7001-7004
7126542 CIFC17 H23.25 B10 NP n m a10.6954; 10.2783; 18.0417
90; 90; 90		1983.33Chen, Yu; Quan, Yangjian; Xie, Zuowei
Ir-catalyzed selective dehydrogenative cross-coupling of aryls with o-carboranes via a mixed directing-group strategy.
Chemical communications (Cambridge, England), 2020, 56, 7001-7004
7126543 CIFC26 H35 B10 F3 Ir N O2P -111.8847; 12.265; 12.2774
90.795; 114.061; 106.385		1550.7Chen, Yu; Quan, Yangjian; Xie, Zuowei
Ir-catalyzed selective dehydrogenative cross-coupling of aryls with o-carboranes via a mixed directing-group strategy.
Chemical communications (Cambridge, England), 2020, 56, 7001-7004
7126544 CIFC28 H44 Br2 O2 S2 Si2C 1 2/c 112.1566; 9.5772; 28.031
90; 92.526; 90		3260.4Tani, Yosuke; Komura, Mao; Ogawa, Takuji
Mechanoresponsive turn-on phosphorescence by a desymmetrization approach.
Chemical communications (Cambridge, England), 2020, 56, 6810-6813
7126545 CIFC28 H44 Br2 O2 S2 Si2C 1 2/c 112.2294; 9.613; 28.292
90; 93.195; 90		3320.9Tani, Yosuke; Komura, Mao; Ogawa, Takuji
Mechanoresponsive turn-on phosphorescence by a desymmetrization approach.
Chemical communications (Cambridge, England), 2020, 56, 6810-6813
7126546 CIFC28 H45 Br O2 S2 Si2C 1 c 112.2344; 9.4516; 27.594
90; 91.677; 90		3189.5Tani, Yosuke; Komura, Mao; Ogawa, Takuji
Mechanoresponsive turn-on phosphorescence by a desymmetrization approach.
Chemical communications (Cambridge, England), 2020, 56, 6810-6813
7126547 CIFC28 H44 Br2 O2 S2 Si2C 1 2/c 112.257; 9.6358; 28.442
90; 93.474; 90		3353Tani, Yosuke; Komura, Mao; Ogawa, Takuji
Mechanoresponsive turn-on phosphorescence by a desymmetrization approach.
Chemical communications (Cambridge, England), 2020, 56, 6810-6813
7126548 CIFC28 H44 Br2 O2 S2 Si2C 1 2/c 112.2; 9.5964; 28.151
90; 92.89; 90		3291.6Tani, Yosuke; Komura, Mao; Ogawa, Takuji
Mechanoresponsive turn-on phosphorescence by a desymmetrization approach.
Chemical communications (Cambridge, England), 2020, 56, 6810-6813
7126549 CIFC28 H45 Br O2 S2 Si2C 1 c 112.2742; 9.4757; 27.688
90; 92.029; 90		3218.3Tani, Yosuke; Komura, Mao; Ogawa, Takuji
Mechanoresponsive turn-on phosphorescence by a desymmetrization approach.
Chemical communications (Cambridge, England), 2020, 56, 6810-6813
7126550 CIFC28 H45 Br O2 S2 Si2C 1 c 112.339; 9.5268; 27.927
90; 92.563; 90		3279.6Tani, Yosuke; Komura, Mao; Ogawa, Takuji
Mechanoresponsive turn-on phosphorescence by a desymmetrization approach.
Chemical communications (Cambridge, England), 2020, 56, 6810-6813
7126551 CIFC28 H45 Br O2 S2 Si2C 1 c 112.362; 9.5472; 28.028
90; 92.689; 90		3304.3Tani, Yosuke; Komura, Mao; Ogawa, Takuji
Mechanoresponsive turn-on phosphorescence by a desymmetrization approach.
Chemical communications (Cambridge, England), 2020, 56, 6810-6813
7126552 CIFC28 H44 Br2 O2 S2 Si2C 1 2/c 112.2729; 9.6494; 28.534
90; 93.614; 90		3372.5Tani, Yosuke; Komura, Mao; Ogawa, Takuji
Mechanoresponsive turn-on phosphorescence by a desymmetrization approach.
Chemical communications (Cambridge, England), 2020, 56, 6810-6813
7126553 CIFC28 H45 Br O2 S2 Si2C 1 c 112.3126; 9.505; 27.815
90; 92.26; 90		3252.7Tani, Yosuke; Komura, Mao; Ogawa, Takuji
Mechanoresponsive turn-on phosphorescence by a desymmetrization approach.
Chemical communications (Cambridge, England), 2020, 56, 6810-6813
7126554 CIFC65 H74 Br N2 O3 ReP 1 21/c 120.709; 10.9734; 25.4961
90; 95.441; 90		5767.8Salsi, Federico; Neville, Michael; Drance, Myles; Hagenbach, Adelheid; Chan, Chinglin; Figueroa, Joshua S.; Abram, Ulrich
A closed-shell monomeric rhenium(1-) anion provided by m-terphenyl isocyanide ligation.
Chemical communications (Cambridge, England), 2020, 56, 7009-7012
7126555 CIFC65 H74 K N2 O3 ReP -110.5021; 12.1274; 25.1217
84.635; 87.156; 66.182		2914Salsi, Federico; Neville, Michael; Drance, Myles; Hagenbach, Adelheid; Chan, Chinglin; Figueroa, Joshua S.; Abram, Ulrich
A closed-shell monomeric rhenium(1-) anion provided by m-terphenyl isocyanide ligation.
Chemical communications (Cambridge, England), 2020, 56, 7009-7012
7126556 CIFC65 H74 Br N2 O3 ReC 1 2/c 124.0967; 24.0107; 21.223
90; 108.41; 90		11651Salsi, Federico; Neville, Michael; Drance, Myles; Hagenbach, Adelheid; Chan, Chinglin; Figueroa, Joshua S.; Abram, Ulrich
A closed-shell monomeric rhenium(1-) anion provided by m-terphenyl isocyanide ligation.
Chemical communications (Cambridge, England), 2020, 56, 7009-7012
7126557 CIFC6 H13 F I NP 1 21 15.9613; 7.6228; 10.163
90; 105.627; 90		444.75Ai, Yong; Wu, Dong-Ji; Yang, Meng-Juan; Wang, Pan; He, Wen-Hui; Liao, Wei-Qiang
Highest-T<sub>c</sub> organic enantiomeric ferroelectrics obtained by F/H substitution.
Chemical communications (Cambridge, England), 2020, 56, 7033-7036
7126558 CIFC6 H14 I NP 1 21/n 17.2325; 11.9157; 10.4951
90; 94.932; 90		901.12Ai, Yong; Wu, Dong-Ji; Yang, Meng-Juan; Wang, Pan; He, Wen-Hui; Liao, Wei-Qiang
Highest-T<sub>c</sub> organic enantiomeric ferroelectrics obtained by F/H substitution.
Chemical communications (Cambridge, England), 2020, 56, 7033-7036
7126559 CIFC6 H13 F I NP 1 21/c 17.2723; 10.4559; 11.9429
90; 97.868; 90		899.57Ai, Yong; Wu, Dong-Ji; Yang, Meng-Juan; Wang, Pan; He, Wen-Hui; Liao, Wei-Qiang
Highest-T<sub>c</sub> organic enantiomeric ferroelectrics obtained by F/H substitution.
Chemical communications (Cambridge, England), 2020, 56, 7033-7036
7126560 CIFC6 H13 F I NP 1 21 15.9585; 7.6205; 10.1558
90; 105.571; 90		444.22Ai, Yong; Wu, Dong-Ji; Yang, Meng-Juan; Wang, Pan; He, Wen-Hui; Liao, Wei-Qiang
Highest-T<sub>c</sub> organic enantiomeric ferroelectrics obtained by F/H substitution.
Chemical communications (Cambridge, England), 2020, 56, 7033-7036
7126561 CIFC10 H17 N5 O7 SC 1 2 123.123; 9.7734; 6.3397
90; 91.2914; 90		1432.3Xiao, Songjun; Lee, Wes; Chen, Fu; Zavalij, Peter Y.; Gutierrez, Osvaldo; Davis, Jeffery T.
Oxidation of 8-thioguanosine gives redox-responsive hydrogels and reveals intermediates in a desulfurization pathway.
Chemical communications (Cambridge, England), 2020, 56, 6981-6984
7126562 CIFC221 H195 Au20 Cl10 F18 O P12 Sb3P -122.0586; 23.0723; 26.8383
105.276; 92.8279; 108.247		12383.7Yuan, Shang-Fu; Li, Jiao-Jiao; Guan, Zong-Jie; Lei, Zhen; Wang, Quan-Ming
Ultrastable hydrido gold nanoclusters with the protection of phosphines.
Chemical communications (Cambridge, England), 2020, 56, 7037-7040
7126563 CIFC456 H418 Au40 F36 O16 P30 S2P 1 21/n 121.5346; 43.3916; 27.32
90; 90.8269; 90		25525.7Yuan, Shang-Fu; Li, Jiao-Jiao; Guan, Zong-Jie; Lei, Zhen; Wang, Quan-Ming
Ultrastable hydrido gold nanoclusters with the protection of phosphines.
Chemical communications (Cambridge, England), 2020, 56, 7037-7040
7126564 CIFO4 Pb Si SrP 21 21 215.7628; 7.2333; 9.7316
90; 90; 90		405.65Jiang, Shutong; Zhou, Jinjie; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng
PbSrSiO<sub>4</sub>: a new ultraviolet nonlinear optical material with a strong second harmonic generation response and moderate birefringence.
Chemical communications (Cambridge, England), 2020, 56, 7104-7107
7126565 CIFC28 H28 Br N3 OP 1 21 111.3631; 20.5225; 11.963
90; 117.897; 90		2465.6Gao, Zeng; Qian, Jinlong; Yang, Huameng; Hang, Xiao-Chun; Zhang, Jinlong; Jiang, Gaoxi
Chiral Brønsted acid-catalyzed dynamic kinetic resolution of atropisomeric ortho-formyl naphthamides.
Chemical communications (Cambridge, England), 2020, 56, 7265-7268
7126566 CIFC28 H29 N3 OP 1 21 112.0096; 13.3196; 16.1216
90; 109.131; 90		2436.4Gao, Zeng; Qian, Jinlong; Yang, Huameng; Hang, Xiao-Chun; Zhang, Jinlong; Jiang, Gaoxi
Chiral Brønsted acid-catalyzed dynamic kinetic resolution of atropisomeric ortho-formyl naphthamides.
Chemical communications (Cambridge, England), 2020, 56, 7265-7268
7126567 CIFC21 H16 O3P 1 21/n 19.2055; 17.4289; 10.2408
90; 92.039; 90		1642.01Li, Yongfeng; Tang, Zhiqiong; Zhang, Junliang; Liu, Lu
Gold-catalyzed intermolecular [4+1] spiroannulation via site-selective aromatic C(sp<sup>2</sup>)-H functionalization and dearomatization of phenol derivatives.
Chemical communications (Cambridge, England), 2020, 56, 8202-8205
7126568 CIFC21 H16 O3P 1 21/n 18.1264; 13.3342; 14.6256
90; 93.275; 90		1582.23Li, Yongfeng; Tang, Zhiqiong; Zhang, Junliang; Liu, Lu
Gold-catalyzed intermolecular [4+1] spiroannulation via site-selective aromatic C(sp<sup>2</sup>)-H functionalization and dearomatization of phenol derivatives.
Chemical communications (Cambridge, England), 2020, 56, 8202-8205
7126569 CIFC42 H32 O6P -110.5466; 10.572; 14.2364
88.049; 84.217; 86.299		1575.36Li, Yongfeng; Tang, Zhiqiong; Zhang, Junliang; Liu, Lu
Gold-catalyzed intermolecular [4+1] spiroannulation via site-selective aromatic C(sp<sup>2</sup>)-H functionalization and dearomatization of phenol derivatives.
Chemical communications (Cambridge, England), 2020, 56, 8202-8205
7126570 CIFC72 H84 O4 P2 PtP -19.7763; 10.5375; 15.1911
90.931; 90.634; 93.521		1561.7Mullin, William J.; Qin, Huan; Mani, Tomoyasu; Müller, Peter; Panzer, Matthew J.; Thomas, Samuel W.
Turning on solid-state phosphorescence of platinum acetylides with aromatic stacking.
Chemical communications (Cambridge, England), 2020, 56, 6854-6857
7126571 CIFC66 H88 O4 P2 PtP -19.068; 10.8256; 15.2471
94.454; 91.432; 92.084		1490.7Mullin, William J.; Qin, Huan; Mani, Tomoyasu; Müller, Peter; Panzer, Matthew J.; Thomas, Samuel W.
Turning on solid-state phosphorescence of platinum acetylides with aromatic stacking.
Chemical communications (Cambridge, England), 2020, 56, 6854-6857
7126572 CIFC72 H74 F10 O4 P2 PtP 1 21/m 114.8762; 14.6209; 14.9832
90; 90.35; 90		3258.8Mullin, William J.; Qin, Huan; Mani, Tomoyasu; Müller, Peter; Panzer, Matthew J.; Thomas, Samuel W.
Turning on solid-state phosphorescence of platinum acetylides with aromatic stacking.
Chemical communications (Cambridge, England), 2020, 56, 6854-6857
7126573 CIFC72 H74 F10 O4 P2 PtP -117.9125; 21.095; 21.0976
60.1816; 89.8948; 76.3364		6657.3Mullin, William J.; Qin, Huan; Mani, Tomoyasu; Müller, Peter; Panzer, Matthew J.; Thomas, Samuel W.
Turning on solid-state phosphorescence of platinum acetylides with aromatic stacking.
Chemical communications (Cambridge, England), 2020, 56, 6854-6857
7126574 CIFC12 H5 F3.33 N0.33 O0.67P -110.3014; 11.5202; 12.2962
96.803; 97.658; 98.459		1416.24Casali, Emanuele; Kalra, Prakriti; Brochetta, Massimo; Borsari, Tania; Gandini, Andrea; Patra, Tuhin; Zanoni, Giuseppe; Maiti, Debabrata
Overriding ortho selectivity by template assisted meta-C-H activation of benzophenones.
Chemical communications (Cambridge, England), 2020, 56, 7281-7284
7126575 CIFC11 H13 N2 S SeP n a 217.3132; 15.406; 10.7773
90; 90; 90		1214.25Karri, Ramesh; Das, Ranajit; Rai, Rakesh Kumar; Gopalakrishnan, Anaswara; Roy, Gouriprasanna
Hg-C bond protonolysis by a functional model of bacterial enzyme organomercurial lyase MerB.
Chemical communications (Cambridge, England), 2020, 56, 9280-9283
7126576 CIFC13 H16 N2 S SeC 1 2 119.541; 7.511; 20.264
90; 113.102; 90		2735.7Karri, Ramesh; Das, Ranajit; Rai, Rakesh Kumar; Gopalakrishnan, Anaswara; Roy, Gouriprasanna
Hg-C bond protonolysis by a functional model of bacterial enzyme organomercurial lyase MerB.
Chemical communications (Cambridge, England), 2020, 56, 9280-9283
7126577 CIFC14 H24 N4 O2 S2 Se2P b c n34.65; 4.9196; 12.0074
90; 90; 90		2046.8Karri, Ramesh; Das, Ranajit; Rai, Rakesh Kumar; Gopalakrishnan, Anaswara; Roy, Gouriprasanna
Hg-C bond protonolysis by a functional model of bacterial enzyme organomercurial lyase MerB.
Chemical communications (Cambridge, England), 2020, 56, 9280-9283
7126578 CIFC32 H50 Hg N8 O11 Se4C 1 c 123.3194; 14.8183; 16.3857
90; 129.828; 90		4348.4Karri, Ramesh; Das, Ranajit; Rai, Rakesh Kumar; Gopalakrishnan, Anaswara; Roy, Gouriprasanna
Hg-C bond protonolysis by a functional model of bacterial enzyme organomercurial lyase MerB.
Chemical communications (Cambridge, England), 2020, 56, 9280-9283
7126579 CIFC10 H13 Hg I N2 SeP 1 21/c 18.4028; 18.7925; 8.9951
90; 104.092; 90		1377.67Karri, Ramesh; Das, Ranajit; Rai, Rakesh Kumar; Gopalakrishnan, Anaswara; Roy, Gouriprasanna
Hg-C bond protonolysis by a functional model of bacterial enzyme organomercurial lyase MerB.
Chemical communications (Cambridge, England), 2020, 56, 9280-9283
7126580 CIFC6 H11 Hg I N2 SeP 1 21/n 18.9682; 10.5369; 11.8452
90; 91.293; 90		1119.05Karri, Ramesh; Das, Ranajit; Rai, Rakesh Kumar; Gopalakrishnan, Anaswara; Roy, Gouriprasanna
Hg-C bond protonolysis by a functional model of bacterial enzyme organomercurial lyase MerB.
Chemical communications (Cambridge, England), 2020, 56, 9280-9283
7126581 CIFC22 H26 N4 S2 Se2P -110.3331; 11.4023; 12.0379
64.466; 79.758; 68.943		1193.89Karri, Ramesh; Das, Ranajit; Rai, Rakesh Kumar; Gopalakrishnan, Anaswara; Roy, Gouriprasanna
Hg-C bond protonolysis by a functional model of bacterial enzyme organomercurial lyase MerB.
Chemical communications (Cambridge, England), 2020, 56, 9280-9283
7126582 CIFC14 H22 B N O2P b c a17.0129; 12.3612; 27.5884
90; 90; 90		5801.8Ilin, Egor A.; Smirnov, Vladimir O.; Volodin, Alexander D.; Korlyukov, Alexander A.; Dilman, Alexander D.
ortho-Dialkylamino arylboranes as efficient reagents for difluorocarbene trapping.
Chemical communications (Cambridge, England), 2020, 56, 7140-7142
7126583 CIFC17 H24 B F2 N O3P 1 21/c 19.0809; 11.786; 15.8425
90; 95.264; 90		1688.43Ilin, Egor A.; Smirnov, Vladimir O.; Volodin, Alexander D.; Korlyukov, Alexander A.; Dilman, Alexander D.
ortho-Dialkylamino arylboranes as efficient reagents for difluorocarbene trapping.
Chemical communications (Cambridge, England), 2020, 56, 7140-7142
7126584 CIFC15 H22 B F2 N O2P b c a10.6561; 15.0608; 19.6214
90; 90; 90		3149Ilin, Egor A.; Smirnov, Vladimir O.; Volodin, Alexander D.; Korlyukov, Alexander A.; Dilman, Alexander D.
ortho-Dialkylamino arylboranes as efficient reagents for difluorocarbene trapping.
Chemical communications (Cambridge, England), 2020, 56, 7140-7142
7126585 CIFC16 H30 B N Si2 WP -19.1544; 13.25; 17.443
99.524; 102.213; 106.236		1927.7Liu, Siyuan; Légaré, Marc-André; Hofmann, Alexander; Dellermann, Theresa; Braunschweig, Holger
Transition-metal-carbene-like intermolecular insertion of a borylene into C-H bonds.
Chemical communications (Cambridge, England), 2020, 56, 7277-7280
7126586 CIFC49 H108 B4 N4 Si8 W2P 1 21/n 112.0424; 8.8836; 31.436
90; 90.468; 90		3362.9Liu, Siyuan; Légaré, Marc-André; Hofmann, Alexander; Dellermann, Theresa; Braunschweig, Holger
Transition-metal-carbene-like intermolecular insertion of a borylene into C-H bonds.
Chemical communications (Cambridge, England), 2020, 56, 7277-7280
7126587 CIFC33 H27 N O4 SR 3 :H27.6807; 27.6807; 9.6164
90; 90; 120		6381.1Jiang, Bo; Du, Wei; Chen, Ying-Chun
Modified cinchona alkaloid-catalysed enantioselective [4+4] annulations of cyclobutenones and 1-azadienes.
Chemical communications (Cambridge, England), 2020, 56, 7257-7260
7126588 CIFC11 H9 N5C 1 2/c 111.6141; 12.7038; 13.4922
90; 99.08; 90		1965.74Schrage, Briana R.; Nemykin, Victor N.; Ziegler, Christopher J.
Biliazine: a ring open phthalocyanine analog with a meso hydrogen bond.
Chemical communications (Cambridge, England), 2020, 56, 6628-6631
7126589 CIFC24 H21 N9 O2 ZnP 1 21/c 16.8862; 23.1744; 14.2313
90; 102.434; 90		2217.8Schrage, Briana R.; Nemykin, Victor N.; Ziegler, Christopher J.
Biliazine: a ring open phthalocyanine analog with a meso hydrogen bond.
Chemical communications (Cambridge, England), 2020, 56, 6628-6631
7126590 CIFC22 H15 N9P 1 21/n 14.579; 17.112; 23.46
90; 93.02; 90		1836Schrage, Briana R.; Nemykin, Victor N.; Ziegler, Christopher J.
Biliazine: a ring open phthalocyanine analog with a meso hydrogen bond.
Chemical communications (Cambridge, England), 2020, 56, 6628-6631
7126591 CIFC24 H21 Co N9 O2P 1 21/c 16.8635; 23.0498; 14.1576
90; 102.251; 90		2188.8Schrage, Briana R.; Nemykin, Victor N.; Ziegler, Christopher J.
Biliazine: a ring open phthalocyanine analog with a meso hydrogen bond.
Chemical communications (Cambridge, England), 2020, 56, 6628-6631
7126592 CIFC22 H13 Cu N9P 1 21/n 14.6467; 16.7271; 23.289
90; 92.885; 90		1807.9Schrage, Briana R.; Nemykin, Victor N.; Ziegler, Christopher J.
Biliazine: a ring open phthalocyanine analog with a meso hydrogen bond.
Chemical communications (Cambridge, England), 2020, 56, 6628-6631
7126593 CIFC22 H24 O5 PP 1 21 110.2137; 9.2639; 11.792
90; 110.27; 90		1046.6Verma, Ram Subhawan; Khatana, Anil Kumar; Mishra, Monika; Kumar, Shailesh; Tiwari, Bhoopendra
Access to enantioenriched 4-phosphorylated δ-lactones from β-phosphorylenones and enals via carbene organocatalysis.
Chemical communications (Cambridge, England), 2020, 56, 7155-7158
7126594 CIFC22 H20 B F2 N3 OP -17.9478; 8.3539; 14.6488
74.878; 76.982; 83.501		913.27Chen, Yimin; Yuan, Chang; Xie, Tianxin; Li, Yuying; Dai, Bin; Zhou, Kaixiang; Liang, Yi; Dai, Jiapei; Tan, Hongwei; Cui, Mengchao
N,O-Benzamide difluoroboron complexes as near-infrared probes for the detection of β-amyloid and tau fibrils.
Chemical communications (Cambridge, England), 2020, 56, 7269-7272
7126595 CIFC16 H16 N2 O9P 1 21 110.3667; 6.84234; 12.9093
90; 110.345; 90		858.56Ghouilem, Juba; Franco, Rémi; Retailleau, Pascal; Alami, Mouad; Gandon, Vincent; Messaoudi, Samir
Regio- and diastereoselective Pd-catalyzed synthesis of C2-aryl glycosides.
Chemical communications (Cambridge, England), 2020, 56, 7175-7178
7126596 CIFC36 H38 Co2 N30 O44 Si W12C 1 2/c 122.301; 20.14; 17.499
90; 107.336; 90		7503Li, Bonan; Yu, Xiaojing; Pang, Haijun; Shen, Qingbo; Hou, Yan; Ma, Huiyuan; Xin, Jianjiao
Rational regulation of transition metals in polyoxometalate hybrids without noble metal assistance for efficient light-driven H<sub>2</sub> production.
Chemical communications (Cambridge, England), 2020, 56, 7199-7202
7126597 CIFC36 H38 Cd2 N30 O44 Si W12C 1 2/c 122.237; 20.176; 17.67
90; 106.768; 90		7591Li, Bonan; Yu, Xiaojing; Pang, Haijun; Shen, Qingbo; Hou, Yan; Ma, Huiyuan; Xin, Jianjiao
Rational regulation of transition metals in polyoxometalate hybrids without noble metal assistance for efficient light-driven H<sub>2</sub> production.
Chemical communications (Cambridge, England), 2020, 56, 7199-7202
7126598 CIFC36 H38 N30 O44 Si W12 Zn2C 1 2/c 122.386; 19.981; 17.554
90; 107.121; 90		7504Li, Bonan; Yu, Xiaojing; Pang, Haijun; Shen, Qingbo; Hou, Yan; Ma, Huiyuan; Xin, Jianjiao
Rational regulation of transition metals in polyoxometalate hybrids without noble metal assistance for efficient light-driven H<sub>2</sub> production.
Chemical communications (Cambridge, England), 2020, 56, 7199-7202
7126599 CIFC36 H38 Fe2 N30 O44 Si W12C 1 2/c 122.277; 20.082; 17.409
90; 107.033; 90		7447Li, Bonan; Yu, Xiaojing; Pang, Haijun; Shen, Qingbo; Hou, Yan; Ma, Huiyuan; Xin, Jianjiao
Rational regulation of transition metals in polyoxometalate hybrids without noble metal assistance for efficient light-driven H<sub>2</sub> production.
Chemical communications (Cambridge, England), 2020, 56, 7199-7202
7126600 CIFC32 H49 Al N2 O2P -19.6309; 11.5396; 15.2779
103.549; 102.775; 98.081		1576.3Payne, Jack; McKeown, Paul; Kociok-Köhn, Gabriele; Jones, Matthew D.
Novel hybrid aluminium(iii)-catalen complexes as highly active catalysts for lactide polymerisation: towards industrial relevance.
Chemical communications (Cambridge, England), 2020, 56, 7163-7166
7126601 CIFC88.25 H120 Al2 N4 O6P -110.1019; 14.8501; 15.5646
111.216; 103.321; 97.899		2054.4Payne, Jack; McKeown, Paul; Kociok-Köhn, Gabriele; Jones, Matthew D.
Novel hybrid aluminium(iii)-catalen complexes as highly active catalysts for lactide polymerisation: towards industrial relevance.
Chemical communications (Cambridge, England), 2020, 56, 7163-7166
7126602 CIFC81 H94 Al2 Cl4 N4 O6P 1 21/n 19.8297; 29.388; 25.847
90; 94.656; 90		7442Payne, Jack; McKeown, Paul; Kociok-Köhn, Gabriele; Jones, Matthew D.
Novel hybrid aluminium(iii)-catalen complexes as highly active catalysts for lactide polymerisation: towards industrial relevance.
Chemical communications (Cambridge, England), 2020, 56, 7163-7166
7126603 CIFC32 H49 Al N2 O3P 1 21/c 112.4849; 14.4299; 18.0897
90; 91.719; 90		3257.5Payne, Jack; McKeown, Paul; Kociok-Köhn, Gabriele; Jones, Matthew D.
Novel hybrid aluminium(iii)-catalen complexes as highly active catalysts for lactide polymerisation: towards industrial relevance.
Chemical communications (Cambridge, England), 2020, 56, 7163-7166
7126604 CIFC81 H94 Al2 Br4 N4 O6P 1 21/n 19.8437; 29.3; 26.1541
90; 94.073; 90		7524.3Payne, Jack; McKeown, Paul; Kociok-Köhn, Gabriele; Jones, Matthew D.
Novel hybrid aluminium(iii)-catalen complexes as highly active catalysts for lactide polymerisation: towards industrial relevance.
Chemical communications (Cambridge, England), 2020, 56, 7163-7166
7126605 CIFC26 H19 P SP 1 21/c 113.967; 8.892; 17.201
90; 110.46; 90		2001.5Schillmöller, Timo; Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Three colour solid-state luminescence from positional isomers of facilely modified thiophosphoranyl anthracenes.
Chemical communications (Cambridge, England), 2020, 56, 7479-7482
7126606 CIFC26 H19 P SP 1 21/n 19.649; 16.139; 13.295
90; 109.43; 90		1952.5Schillmöller, Timo; Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Three colour solid-state luminescence from positional isomers of facilely modified thiophosphoranyl anthracenes.
Chemical communications (Cambridge, England), 2020, 56, 7479-7482
7126607 CIFC66 H75 Cl4 Cu4 N12 O29.5 S2P b c n18.0508; 17.7526; 24.8923
90; 90; 90		7976.7Khullar, Sadhika; Mandal, Sanjay K.
Modulation of hydrophilicity inside the cavity of molecular rectangles self-assembled under ambient conditions.
Chemical communications (Cambridge, England), 2020, 56, 7913-7916
7126608 CIFC68 H80 Cl4 Cu4 N12 O30 S2P -115.352; 15.546; 19.838
73.309; 78.299; 63.132		4031Khullar, Sadhika; Mandal, Sanjay K.
Modulation of hydrophilicity inside the cavity of molecular rectangles self-assembled under ambient conditions.
Chemical communications (Cambridge, England), 2020, 56, 7913-7916
7126609 CIFC70 H86 Cl4 Cu4 N12 O31 S2P 1 c 120.1897; 13.6168; 16.2901
90; 108.38; 90		4250Khullar, Sadhika; Mandal, Sanjay K.
Modulation of hydrophilicity inside the cavity of molecular rectangles self-assembled under ambient conditions.
Chemical communications (Cambridge, England), 2020, 56, 7913-7916
7126610 CIFC22 H42 I2 Mo N P2P b c a18.6834; 18.4365; 16.0574
90; 90; 90		5531.1Tanabe, Yoshiaki; Sekiguchi, Yoshiya; Tanaka, Hiromasa; Konomi, Asuka; Yoshizawa, Kazunari; Kuriyama, Shogo; Nishibayashi, Yoshiaki
Preparation and reactivity of molybdenum complexes bearing pyrrole-based PNP-type pincer ligand.
Chemical communications (Cambridge, England), 2020, 56, 6933-6936

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