Crystallography Open Database

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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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