Crystallography Open Database

Result: there are 11338 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format

We are unable to provide that many records as a single archive.
You can instead download the entire COD archive as a single .zip, .tgz or .txz archive.

Searching year of publication is 2022

Blue left arrow Blue left arrow First | Blue left arrow Previous 300 | of 38 | Next 300 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1567478 CIFC31 H25 F7 N3 Ni O3P 21 21 2111.0205; 13.9185; 19.0776
90; 90; 90
2926.29Delamare, Aline; Naulet, Guillaume; Kauffmann, Brice; Guichard, Gilles; Compain, Guillaume
Hexafluoroisobutylation of enolates through a tandem elimination/allylic shift/hydrofluorination reaction
Chemical Science, 2022, 13, 9507-9514
1567479 CIFC7 H4 F6 N2P 1 21/c 113.7855; 5.6753; 11.6678
90; 103.923; 90
886.03Delamare, Aline; Naulet, Guillaume; Kauffmann, Brice; Guichard, Gilles; Compain, Guillaume
Hexafluoroisobutylation of enolates through a tandem elimination/allylic shift/hydrofluorination reaction
Chemical Science, 2022, 13, 9507-9514
1567480 CIFC48 H38 N6 OC 1 2/c 118.1467; 14.4007; 32.924
90; 95.169; 90
8568.9Qu, Jiamin; Zhang, Yahui; Cai, Zhengxu; Tong, Bin; Xie, Hai-Yan; Dong, Yuping; Shi, Jianbing
An Acceptor-Shielding Strategy of Photosensitizer for Enhancing the Generation Efficiency of Type I Reactive Oxygen Species and the Related Photodynamic Immunotherapy
Nanoscale, 2022
1567481 CIFC48 H30 B N3P 1 21/c 114.234; 19.457; 12.568
90; 100.195; 90
3425.8He, Shuang; Liu, Junjie; Yang, Ge; Bin, Zhengyang; You, Jingsong
Dipole moment engineering enables universal B-N-embedded bipolar hosts for OLEDs: an old dog learns a new trick.
Materials horizons, 2022, 9, 2818-2823
1567482 CIFC54 H42 B N3C 1 2/c 127.5838; 9.1201; 19.3361
90; 124.586; 90
4004.7He, Shuang; Liu, Junjie; Yang, Ge; Bin, Zhengyang; You, Jingsong
Dipole moment engineering enables universal B-N-embedded bipolar hosts for OLEDs: an old dog learns a new trick.
Materials horizons, 2022, 9, 2818-2823
1567483 CIFC21 H18 N2 O2P -18.0404; 9.2472; 11.6115
85.805; 74.493; 77.63
812.47Sun, Xi-Shang; Diao, Xin-Yu; Dong, Xiu-Qin; Wang, Chun-Jiang
Base-Promoted Cascade β-F-Elimination/Electrocyclization/Diels-Alder/Retro-Diels-Alder Reaction: Efficient Access to δ-Carboline Derivatives
Chemical Science, 2022
1567484 CIFC20 H16 F2 N2 O3P -110.4381; 17.2549; 20.9737
108.139; 90.02; 107.606
3403Sun, Xi-Shang; Diao, Xin-Yu; Dong, Xiu-Qin; Wang, Chun-Jiang
Base-Promoted Cascade β-F-Elimination/Electrocyclization/Diels-Alder/Retro-Diels-Alder Reaction: Efficient Access to δ-Carboline Derivatives
Chemical Science, 2022
1567485 CIFC143 H198 Dy6 N43 O75P 1 21/n 125.48; 23.024; 39.629
90; 90.666; 90
23247Li, Xiao-Lei; Zhao, Lang; Wu, Jianfeng; Shi, Wei; Struch, Niklas; Lützen, Arne; Powell, Annie K.; Cheng, Peng; Tang, Jinkui
Subcomponent self-assembly of circular helical Dy6(L)6 and bipyramid Dy12(L)8 architectures directed via second-order template effects
Chemical Science, 2022
1567486 CIFC224 H222 Dy12 N50 Na4 O94I 41/a c d :232.0539; 32.0539; 56.6487
90; 90; 90
58204Li, Xiao-Lei; Zhao, Lang; Wu, Jianfeng; Shi, Wei; Struch, Niklas; Lützen, Arne; Powell, Annie K.; Cheng, Peng; Tang, Jinkui
Subcomponent self-assembly of circular helical Dy6(L)6 and bipyramid Dy12(L)8 architectures directed via second-order template effects
Chemical Science, 2022
1567487 CIFC16 H17 N O2 S2P 21 21 216.2635; 11.4411; 20.8675
90; 90; 90
1495.4Lai, Junshan; Reid, Jolene P.
Interrogating the thionium hydrogen bond as a noncovalent stereocontrolling interaction in chiral phosphate catalysis
Chemical Science, 2022, 13, 11065-11073
1567491 CIFC22 H20 Cl2 N2 O2 SP 1 21/c 123.213; 6.0771; 30.525
90; 151.09; 90
2082Gurung, Bikram; Pradhan, Sajan; Sharma, Debesh; Bhujel, Deshaj; Basel, Siddhant; Chettri, Shivanand; Rasaily, Sagarmani; Pariyar, Anand; Tamang, Sudarsan
CsPbBr3 perovskite quantum dots as a visible light photocatalyst for cyclisation of diamines and amino alcohols: an efficient approach to synthesize imidazolidines, fused-imidazolidines and oxazolidines
Catalysis Science & Technology, 2022, 12, 5891-5898
1567492 CIFC33 H27 B F5 N3 OP 1 21/c 18.5951; 13.507; 25.5281
90; 99.612; 90
2922.1Chen, Chaohuang; Daniliuc, Constantin Gabriel; Klabunde, Sina; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Generation of Boryl-nitroxide Radicals from a Boraalkene via the Nitroso Ene Reaction
Chemical Science, 2022
1567493 CIFC39 H38 B F5 N3 OP 1 21/n 114.1129; 16.9245; 15.4437
90; 111.527; 90
3431.47Chen, Chaohuang; Daniliuc, Constantin Gabriel; Klabunde, Sina; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Generation of Boryl-nitroxide Radicals from a Boraalkene via the Nitroso Ene Reaction
Chemical Science, 2022
1567494 CIFC39 H38 B F5 N3 OI 41/a :223.5399; 23.5399; 24.957
90; 90; 90
13829.3Chen, Chaohuang; Daniliuc, Constantin Gabriel; Klabunde, Sina; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Generation of Boryl-nitroxide Radicals from a Boraalkene via the Nitroso Ene Reaction
Chemical Science, 2022
1567495 CIFC39 H39 B F5 N3 OP 1 21/c 116.5547; 10.2914; 20.8535
90; 110.198; 90
3334.4Chen, Chaohuang; Daniliuc, Constantin Gabriel; Klabunde, Sina; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Generation of Boryl-nitroxide Radicals from a Boraalkene via the Nitroso Ene Reaction
Chemical Science, 2022
1567496 CIFC33 H33 B F6 N2P 1 21/n 110.2547; 17.4775; 16.6351
90; 98.497; 90
2948.73Chen, Chaohuang; Daniliuc, Constantin Gabriel; Klabunde, Sina; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Generation of Boryl-nitroxide Radicals from a Boraalkene via the Nitroso Ene Reaction
Chemical Science, 2022
1567497 CIFC39 H39 B F5 N3 OP 1 21/c 19.5222; 18.1892; 19.3469
90; 94.624; 90
3340Chen, Chaohuang; Daniliuc, Constantin Gabriel; Klabunde, Sina; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Generation of Boryl-nitroxide Radicals from a Boraalkene via the Nitroso Ene Reaction
Chemical Science, 2022
1567498 CIFC45 H46 Cl2 N2 O2P -18.6461; 14.5796; 15.3848
99.024; 95.585; 104.779
1832.74Bartkowski, Krzysztof; Zimmermann Crocomo, Paola; Kochman, Michał Andrzej; Kumar, Dharmandra; Kubas, Adam; Data, Przemysław; Lindner, Marcin
Tandem rigidification and π-extension as a key tool for the development of a narrow linewidth yellow hyperfluorescent OLED system
Chemical Science, 2022
1567499 CIFC63.4 H61 N3 O2P b c n11.8808; 10.3821; 42.031
90; 90; 90
5184.4Bartkowski, Krzysztof; Zimmermann Crocomo, Paola; Kochman, Michał Andrzej; Kumar, Dharmandra; Kubas, Adam; Data, Przemysław; Lindner, Marcin
Tandem rigidification and π-extension as a key tool for the development of a narrow linewidth yellow hyperfluorescent OLED system
Chemical Science, 2022
1567500 CIFC44 H46 N2 O2P 1 21/c 117.2674; 9.762; 22.2538
90; 108.27; 90
3562.1Bartkowski, Krzysztof; Zimmermann Crocomo, Paola; Kochman, Michał Andrzej; Kumar, Dharmandra; Kubas, Adam; Data, Przemysław; Lindner, Marcin
Tandem rigidification and π-extension as a key tool for the development of a narrow linewidth yellow hyperfluorescent OLED system
Chemical Science, 2022
1567501 CIF
HKL
Paper
C24 H27 I N2 O SP -18.478; 10.5773; 14.5191
95.81; 105.762; 110.651
1144.1Shank, Nathaniel; Stadler, Andrea L.; Barrett, Sean P.; Padgett, Clifford W.
1-(Hex-5-en-1-yl)-4-{[3-methyl-2,3-dihydro-1,3-benzothiazol-2-ylidene]methyl}quinolin-1-ium iodide monohydrate
IUCrData, 2022, 7, x220797
1567502 CIFC32 H22 N6 O4P 1 21/c 111.0961; 9.9627; 22.3275
90; 94.43; 90
2460.87Hamsath, Akil; Lederberg, Oren L.; Cui, Qi; Shieh, Meg; Lam, Yannie; Brummett, Brock J.; Xu, Shi; Robinson, Jerome R.; Xian, Ming
Intramolecular tetrazine-acryloyl cycloaddition: chemistry and applications
Chemical Science, 2022
1567503 CIFC26 H22 Cl2 N8 O8 RuP b c n8.1943; 21.1329; 16.5436
90; 90; 90
2864.8Pokhrel, Indira; Reddy, Guda Dinneswara; Kwon, Taejin; Choi, Eungyeong; Chun, Yu Sung; Lee, Sang Tak; Sung, Bong June; Lee, Duck Hyung; Bin Oh, Han; Yoon, Kyung Byung
Insights into the directions to increase turnover frequency and turnover number during photochemical water oxidation with molecular Ru catalysts
Energy & Environmental Science, 2022, 15, 4259-4288
1567504 CIFC24 H24 Cl2 N10 O8 RuC 1 2/c 117.8962; 10.2796; 15.9597
90; 90.899; 90
2935.68Pokhrel, Indira; Reddy, Guda Dinneswara; Kwon, Taejin; Choi, Eungyeong; Chun, Yu Sung; Lee, Sang Tak; Sung, Bong June; Lee, Duck Hyung; Bin Oh, Han; Yoon, Kyung Byung
Insights into the directions to increase turnover frequency and turnover number during photochemical water oxidation with molecular Ru catalysts
Energy & Environmental Science, 2022, 15, 4259-4288
1567505 CIFC30 H29 F12 N9 P2 RuP -18.2606; 10.798; 20.5518
77.5866; 84.0528; 84.8406
1776.36Pokhrel, Indira; Reddy, Guda Dinneswara; Kwon, Taejin; Choi, Eungyeong; Chun, Yu Sung; Lee, Sang Tak; Sung, Bong June; Lee, Duck Hyung; Bin Oh, Han; Yoon, Kyung Byung
Insights into the directions to increase turnover frequency and turnover number during photochemical water oxidation with molecular Ru catalysts
Energy & Environmental Science, 2022, 15, 4259-4288
1567506 CIF
HKL
B Fe O3R -3 c :H4.251; 4.251; 11.772
90; 90; 120
184.23Dong, Weiwei; Glazyrin, Konstantin; Khandarkhaeva, Saiana; Fedotenko, Timofey; Bednarčík, Jozef; Greenberg, Eran; Dubrovinsky, Leonid; Dubrovinskaia, Natalia; Liermann, Hanns-Peter
Fe~0.79~Si~0.07~B~0.14~ metallic glass gaskets for high-pressure research beyond 1Mbar
Journal of Synchrotron Radiation, 2022, 29, 1167-1179
1567507 CIFC70 H50 Cl2 Ir N3P -113.85396; 14.21567; 14.60645
100.275; 100.655; 105.286
2647.62Yu. Gitlina, Anastasia; Fadaei-Tirani, Farzaneh; Ruggi, Albert; Plaice, Carolina; Severin, Kay
Acid-base-induced fac → mer isomerization of luminescent iridium(iii) complexes
Chemical Science, 2022
1567508 CIFC23 H17 NP 1 21/c 117.7468; 5.5397; 7.8676
90; 95.986; 90
769.26Yu. Gitlina, Anastasia; Fadaei-Tirani, Farzaneh; Ruggi, Albert; Plaice, Carolina; Severin, Kay
Acid-base-induced fac → mer isomerization of luminescent iridium(iii) complexes
Chemical Science, 2022
1567509 CIFC34 H22 F4 Ir N3C 1 2/c 133.9701; 8.77822; 18.031
90; 98.898; 90
5312.08Yu. Gitlina, Anastasia; Fadaei-Tirani, Farzaneh; Ruggi, Albert; Plaice, Carolina; Severin, Kay
Acid-base-induced fac → mer isomerization of luminescent iridium(iii) complexes
Chemical Science, 2022
1567510 CIFC35.5 H26 Cl F6 Ir N4 O4 S2P 1 21/c 127.8756; 12.7084; 20.40752
90; 104.608; 90
6995.75Yu. Gitlina, Anastasia; Fadaei-Tirani, Farzaneh; Ruggi, Albert; Plaice, Carolina; Severin, Kay
Acid-base-induced fac → mer isomerization of luminescent iridium(iii) complexes
Chemical Science, 2022
1567511 CIFC69 H48 Ir N3P -118.08; 18.3585; 19.0127
68.335; 85.431; 64.368
5263.6Yu. Gitlina, Anastasia; Fadaei-Tirani, Farzaneh; Ruggi, Albert; Plaice, Carolina; Severin, Kay
Acid-base-induced fac → mer isomerization of luminescent iridium(iii) complexes
Chemical Science, 2022
1567512 CIFC33 H24 Ir N3P 41 21 29.72023; 9.72023; 30.5949
90; 90; 90
2890.69Yu. Gitlina, Anastasia; Fadaei-Tirani, Farzaneh; Ruggi, Albert; Plaice, Carolina; Severin, Kay
Acid-base-induced fac → mer isomerization of luminescent iridium(iii) complexes
Chemical Science, 2022
1567513 CIFC13 H11C 1 2/c 117.661; 5.8999; 17.598
90; 91.211; 90
1833.3Kurosawa, Miki B.; Kato, Kenta; Muto, Kei; Yamaguchi, Junichiro
Unified Synthesis of Multiply Arylated Alkanes by Catalytic Deoxygenative Transformation of Diarylketones
Chemical Science, 2022
1567514 CIFC30 H26P -19.9103; 10.3946; 10.4347
98.955; 91.413; 103.689
1029.5Kurosawa, Miki B.; Kato, Kenta; Muto, Kei; Yamaguchi, Junichiro
Unified Synthesis of Multiply Arylated Alkanes by Catalytic Deoxygenative Transformation of Diarylketones
Chemical Science, 2022
1567515 CIFC27 H20 OP 1 21 17.3391; 10.8689; 11.7668
90; 96.085; 90
933.33Kurosawa, Miki B.; Kato, Kenta; Muto, Kei; Yamaguchi, Junichiro
Unified Synthesis of Multiply Arylated Alkanes by Catalytic Deoxygenative Transformation of Diarylketones
Chemical Science, 2022
1567516 CIFC26 H36 O6P 21 21 219.7178; 15.2909; 15.5463
90; 90; 90
2310.09Tang, Jia; Matsuda, Yudai
Discovery of branching meroterpenoid biosynthetic pathways in Aspergillus insuetus: involvement of two terpene cyclases with distinct cyclization modes
Chemical Science, 2022
1567517 CIFC26 H34 O5P 21 21 218.3273; 13.7746; 19.8852
90; 90; 90
2280.94Tang, Jia; Matsuda, Yudai
Discovery of branching meroterpenoid biosynthetic pathways in Aspergillus insuetus: involvement of two terpene cyclases with distinct cyclization modes
Chemical Science, 2022
1567518 CIFC26 H36 O5P 21 21 218.253; 12.0228; 23.2817
90; 90; 90
2310.11Tang, Jia; Matsuda, Yudai
Discovery of branching meroterpenoid biosynthetic pathways in Aspergillus insuetus: involvement of two terpene cyclases with distinct cyclization modes
Chemical Science, 2022
1567519 CIFC26 H40 O5P 21 21 217.5943; 14.3966; 21.25
90; 90; 90
2323.31Tang, Jia; Matsuda, Yudai
Discovery of branching meroterpenoid biosynthetic pathways in Aspergillus insuetus: involvement of two terpene cyclases with distinct cyclization modes
Chemical Science, 2022
1567520 CIFC26 H38 O7P 1 21 18.2802; 11.1074; 13.0738
90; 90.752; 90
1202.31Tang, Jia; Matsuda, Yudai
Discovery of branching meroterpenoid biosynthetic pathways in Aspergillus insuetus: involvement of two terpene cyclases with distinct cyclization modes
Chemical Science, 2022
1567521 CIFC26.75 H41 O6.75P 110.086; 15.2512; 17.1263
91.211; 99.494; 98.375
2567.88Tang, Jia; Matsuda, Yudai
Discovery of branching meroterpenoid biosynthetic pathways in Aspergillus insuetus: involvement of two terpene cyclases with distinct cyclization modes
Chemical Science, 2022
1567522 CIFC34 H36 Cl P2 RhP 110.3091; 12.7665; 13.3424
107.864; 101.093; 112.099
1451.17Som, Salina; Choi, Jongwook; Katsoulis, Dimitris; Lee, Kangsang L.
Direct Method to Access Various Functional Arylalkoxysilanes by Rh-catalysed Intermolecular C–H Silylation of Alkoxysilane
Chemical Science, 2022
1567523 CIFC68 H72 P4 Rh2P 21 21 2113.1998; 18.0969; 24.5076
90; 90; 90
5854.3Som, Salina; Choi, Jongwook; Katsoulis, Dimitris; Lee, Kangsang L.
Direct Method to Access Various Functional Arylalkoxysilanes by Rh-catalysed Intermolecular C–H Silylation of Alkoxysilane
Chemical Science, 2022
1567524 CIFC34 H36.5 Cl0.5 P2 RhP 21 21 2110.8094; 22.1084; 24.464
90; 90; 90
5846.4Som, Salina; Choi, Jongwook; Katsoulis, Dimitris; Lee, Kangsang L.
Direct Method to Access Various Functional Arylalkoxysilanes by Rh-catalysed Intermolecular C–H Silylation of Alkoxysilane
Chemical Science, 2022
1567525 CIFC29 H45 N O8 SP 1 21 19.8124; 10.5313; 27.852
90; 90.936; 90
2877.8Kukor, Andrew J.; Depner, Noah; Cai, Isabelle; Tucker, John; Culhane, Jeffrey C.; Hein, Jason E.
Enantioselective Synthesis of (-)-Tetrabenazine Via Continuous Crystallization-Induced Diastereomer Transformation
Chemical Science, 2022
1567526 CIFC28 H36 N2P -16.2887; 9.7101; 10.801
73.723; 77.522; 79.838
613.42Gonzálvez, Miguel A.; Su, Chuyi; Williams, Craig M.; Bernhardt, Paul V.
Organocopper(ii) complexes: new catalysts for carbon–carbon bond formation via electrochemical atom transfer radical addition (eATRA)
Chemical Science, 2022
1567527 CIFC14 H12 Br NP n a 2111.5971; 17.179; 5.9922
90; 90; 90
1193.81Gonzálvez, Miguel A.; Su, Chuyi; Williams, Craig M.; Bernhardt, Paul V.
Organocopper(ii) complexes: new catalysts for carbon–carbon bond formation via electrochemical atom transfer radical addition (eATRA)
Chemical Science, 2022
1567528 CIFC10 H9 Br2 NP 1 21/c 16.3061; 13.0601; 13.0615
90; 99.138; 90
1062.07Gonzálvez, Miguel A.; Su, Chuyi; Williams, Craig M.; Bernhardt, Paul V.
Organocopper(ii) complexes: new catalysts for carbon–carbon bond formation via electrochemical atom transfer radical addition (eATRA)
Chemical Science, 2022
1567529 CIFC22 H18 F6 N2P 1 21/c 110.666; 12.0851; 8.0892
90; 108.741; 90
987.41Gonzálvez, Miguel A.; Su, Chuyi; Williams, Craig M.; Bernhardt, Paul V.
Organocopper(ii) complexes: new catalysts for carbon–carbon bond formation via electrochemical atom transfer radical addition (eATRA)
Chemical Science, 2022
1567530 CIFC14 H12 Cl NP n a 2111.6527; 16.617; 5.9865
90; 90; 90
1159.18Gonzálvez, Miguel A.; Su, Chuyi; Williams, Craig M.; Bernhardt, Paul V.
Organocopper(ii) complexes: new catalysts for carbon–carbon bond formation via electrochemical atom transfer radical addition (eATRA)
Chemical Science, 2022
1567531 CIFC20 H18 Cl2 N2P 1 21/c 110.5854; 11.8999; 7.675
90; 110.688; 90
904.44Gonzálvez, Miguel A.; Su, Chuyi; Williams, Craig M.; Bernhardt, Paul V.
Organocopper(ii) complexes: new catalysts for carbon–carbon bond formation via electrochemical atom transfer radical addition (eATRA)
Chemical Science, 2022
1567532 CIF
HKL
Paper
C34 H24 F10 Ir N4 O2 PP b c n41.574; 8.6065; 18.2384
90; 90; 90
6525.8Shevlin, Madelyn R.; Stumbo, Emily E.; McMillen, Colin D.; Pienkos, Jared A.
Bis[3,5-difluoro-2-(pyridin-2-yl)phenyl](4,4'-dimethoxy-2,2'-bipyridine)iridium(III) hexafluoridophosphate
IUCrData, 2022, 7, x220830
1567533 CIF
HKL
Paper
C14 H10 Cl4 Fe2 Ga2 O4P 1 21/c 18.3567; 7.0331; 16.5792
90; 91.218; 90
974.2Harakas, George N.; Demmin, Mary Elizabeth
Tetracarbonyldi-μ-chlorido-dichloridobis(η^5^-cyclopentadienyl)diirondigallium(2 <i>Fe{—</i>Ga})
IUCrData, 2022, 7, x220832
1567534 CIF
Paper
C41 H50 N2 O4P -16.0155; 16.5935; 19.2093
101.541; 97.341; 92.928
1857.47Prapakaran, Tulasi; Murugavel, Ramaswamy
4,4'-Methylenebis[<i>N</i>-(2-hydroxy-3-methoxybenzylidene)-2,6-diisopropylaniline]
IUCrData, 2022, 7, x220793
1567535 CIFC28 H26 N4 O2 ZnP 1 2/c 19.7337; 6.0539; 21.73
90; 101.532; 90
1254.6D'Aniello, Sara; Laviéville, Sidonie; Santulli, Federica; Simon, Malaury; Sellitto, Michele; Tedesco, Consiglia; Thomas, Christophe M.; Mazzeo, Mina
Homoleptic phenoxy-imine pyridine zinc complexes: efficient catalysts for solvent free synthesis and chemical degradation of polyesters
Catalysis Science & Technology, 2022, 12, 6142-6154
1567536 CIFC36 H36 N4 O2 ZnP 1 2/n 19.911; 6.0729; 27.229
90; 93.877; 90
1635.1D'Aniello, Sara; Laviéville, Sidonie; Santulli, Federica; Simon, Malaury; Sellitto, Michele; Tedesco, Consiglia; Thomas, Christophe M.; Mazzeo, Mina
Homoleptic phenoxy-imine pyridine zinc complexes: efficient catalysts for solvent free synthesis and chemical degradation of polyesters
Catalysis Science & Technology, 2022, 12, 6142-6154
1567537 CIFC30 H30 N4 O4 ZnC 1 2/c 127.956; 5.988; 19.792
90; 123.7; 90
2756.4D'Aniello, Sara; Laviéville, Sidonie; Santulli, Federica; Simon, Malaury; Sellitto, Michele; Tedesco, Consiglia; Thomas, Christophe M.; Mazzeo, Mina
Homoleptic phenoxy-imine pyridine zinc complexes: efficient catalysts for solvent free synthesis and chemical degradation of polyesters
Catalysis Science & Technology, 2022, 12, 6142-6154
1567538 CIFC33 H39 N O4P 1 21 19.28; 17.0143; 10.0461
90; 115.351; 90
1433.5Balanna, Kuruva; Barik, Soumen; Shee, Sayan; Gonnade, Rajesh G.; Biju, Akkattu T.
Dynamic kinetic resolution of γ,γ-disubstituted indole 2-carboxaldehydes <i>via</i> NHC-Lewis acid cooperative catalysis for the synthesis of tetracyclic ε-lactones.
Chemical science, 2022, 13, 11513-11518
1567539 CIFC52 H84 Ag14 F24 N6 O22 S6C 1 2/c 121.4916; 18.1316; 23.7184
90; 91.945; 90
9237.2Luo, Xi-Ming; Huang, Shuo; Luo, Peng; Ma, Kai; Wang, Zhao-Yang; Dong, Xi-Yan; Zang, Shuang-Quan
Snapshots of key intermediates unveiling the growth from silver ions to Ag70 nanoclusters
Chemical Science, 2022, 13, 11110-11118
1567540 CIFC68 H112 Ag24 F30 N8 O28 S9P -114.2139; 15.6549; 17.3498
94.12; 110.998; 104.208
3439.1Luo, Xi-Ming; Huang, Shuo; Luo, Peng; Ma, Kai; Wang, Zhao-Yang; Dong, Xi-Yan; Zang, Shuang-Quan
Snapshots of key intermediates unveiling the growth from silver ions to Ag70 nanoclusters
Chemical Science, 2022, 13, 11110-11118
1567541 CIFC62 H77 Ag24 F50 N5 O25 S9P -114.9116; 16.3962; 18.2438
97.091; 112.841; 104.162
3864.89Luo, Xi-Ming; Huang, Shuo; Luo, Peng; Ma, Kai; Wang, Zhao-Yang; Dong, Xi-Yan; Zang, Shuang-Quan
Snapshots of key intermediates unveiling the growth from silver ions to Ag70 nanoclusters
Chemical Science, 2022, 13, 11110-11118
1567542 CIFC25 H37 YP 1 21/n 110.1312; 21.6836; 10.1764
90; 99.1673; 90
2207.01Korzyński, Maciej Damian; Bernhardt, Moritz; Romankov, Vladyslav; Dreiser, Jan; Matmon, Guy; Pointillart, Fabrice; Le Guennic, Boris; Cador, Olivier; Copéret, Christophe
Cyclooctatetraenide-based single-ion magnets featuring bulky cyclopentadienyl ligand
Chemical Science, 2022
1567543 CIFC25 H37 NdP 1 21/n 110.1901; 21.8865; 10.2204
90; 98.782; 90
2252.7Korzyński, Maciej Damian; Bernhardt, Moritz; Romankov, Vladyslav; Dreiser, Jan; Matmon, Guy; Pointillart, Fabrice; Le Guennic, Boris; Cador, Olivier; Copéret, Christophe
Cyclooctatetraenide-based single-ion magnets featuring bulky cyclopentadienyl ligand
Chemical Science, 2022
1567544 CIFC25 H37 ErP 1 21/n 110.1016; 21.6348; 10.1842
90; 99.328; 90
2196.3Korzyński, Maciej Damian; Bernhardt, Moritz; Romankov, Vladyslav; Dreiser, Jan; Matmon, Guy; Pointillart, Fabrice; Le Guennic, Boris; Cador, Olivier; Copéret, Christophe
Cyclooctatetraenide-based single-ion magnets featuring bulky cyclopentadienyl ligand
Chemical Science, 2022
1567545 CIFC25 H37 DyP 1 21/n 110.1186; 21.6751; 10.1771
90; 99.224; 90
2203.2Korzyński, Maciej Damian; Bernhardt, Moritz; Romankov, Vladyslav; Dreiser, Jan; Matmon, Guy; Pointillart, Fabrice; Le Guennic, Boris; Cador, Olivier; Copéret, Christophe
Cyclooctatetraenide-based single-ion magnets featuring bulky cyclopentadienyl ligand
Chemical Science, 2022
1567546 CIFC102 H124 F6 K2 Nd4 O6 S2P 1 21/n 121.4669; 18.3458; 25.0418
90; 100.717; 90
9690.1Korzyński, Maciej Damian; Bernhardt, Moritz; Romankov, Vladyslav; Dreiser, Jan; Matmon, Guy; Pointillart, Fabrice; Le Guennic, Boris; Cador, Olivier; Copéret, Christophe
Cyclooctatetraenide-based single-ion magnets featuring bulky cyclopentadienyl ligand
Chemical Science, 2022
1567547 CIFC29 H45 Nd OP b c a18.304; 15.4886; 18.7216
90; 90; 90
5307.64Korzyński, Maciej Damian; Bernhardt, Moritz; Romankov, Vladyslav; Dreiser, Jan; Matmon, Guy; Pointillart, Fabrice; Le Guennic, Boris; Cador, Olivier; Copéret, Christophe
Cyclooctatetraenide-based single-ion magnets featuring bulky cyclopentadienyl ligand
Chemical Science, 2022
1567548 CIFC22 H17 N OP -17.4998; 11.4895; 18.504
98.672; 96.018; 90.007
1567.3Muraoka, Masanobu; Goto, Masahide; Minami, Masaki; Zhou, Dayang; Suzuki, Takeyuki; Yajima, Tatsuo; Hayashi, Jun'ichi; Sogawa, Hiromitsu; Sanda, Fumio
Ethynylene-linked multifunctional benzoxazines: the effect of the ethynylene group and packing on thermal behavior
Polymer Chemistry, 2022, 13, 5590-5596
1567549 CIFC8 H7 N O2F d d 211.8514; 30.185; 7.533
90; 90; 90
2694.8Wang, Bin; Ren, Hongyuan; Cao, Hou-Ji; Lu, Changsheng; Yan, Hong
A switchable redox annulation of 2-nitroarylethanols affording N-heterocycles: photoexcited nitro as a multifunctional handle
Chemical Science, 2022, 13, 11074-11082
1567550 CIFC16 H11 N OR -3 :H35.383; 35.383; 5.235
90; 90; 120
5675.9Wang, Bin; Ren, Hongyuan; Cao, Hou-Ji; Lu, Changsheng; Yan, Hong
A switchable redox annulation of 2-nitroarylethanols affording N-heterocycles: photoexcited nitro as a multifunctional handle
Chemical Science, 2022, 13, 11074-11082
1567551 CIFC34 H25 NP 1 21/n 19.928; 9.4716; 52.455
90; 90.791; 90
4932.1Wang, Bin; Ren, Hongyuan; Cao, Hou-Ji; Lu, Changsheng; Yan, Hong
A switchable redox annulation of 2-nitroarylethanols affording N-heterocycles: photoexcited nitro as a multifunctional handle
Chemical Science, 2022, 13, 11074-11082
1567552 CIFC21 H19 N O3C 1 c 114.0103; 35.603; 11.376
90; 117.174; 90
5048.1Wang, Bin; Ren, Hongyuan; Cao, Hou-Ji; Lu, Changsheng; Yan, Hong
A switchable redox annulation of 2-nitroarylethanols affording N-heterocycles: photoexcited nitro as a multifunctional handle
Chemical Science, 2022, 13, 11074-11082
1567553 CIFC44 H114 N10 Si12 U2I 1 2/a 124.4164; 11.4199; 29.7959
90; 106.683; 90
7958.4Modder, dieuwertje; Batov, Mikhail; Rajeshkumar, Thayalan; Scopelliti, Rosario; Zivkovic, Ivica; Sienkiewicz, Andrzej; Maron, Laurent; Mazzanti, Marinella
Assembling Diuranium Complexes in Different States of Charge with a Bridging Redox-Active Ligand
Chemical Science, 2022
1567554 CIFC34 H48 K N10 O6C 1 2/c 115.3683; 20.526; 14.691
90; 116.777; 90
4137.3Modder, dieuwertje; Batov, Mikhail; Rajeshkumar, Thayalan; Scopelliti, Rosario; Zivkovic, Ivica; Sienkiewicz, Andrzej; Maron, Laurent; Mazzanti, Marinella
Assembling Diuranium Complexes in Different States of Charge with a Bridging Redox-Active Ligand
Chemical Science, 2022
1567555 CIFC62 H150 K N12 O6 Si12 U2I 1 2/a 129.9688; 11.6805; 32.306
90; 115.332; 90
10221.3Modder, dieuwertje; Batov, Mikhail; Rajeshkumar, Thayalan; Scopelliti, Rosario; Zivkovic, Ivica; Sienkiewicz, Andrzej; Maron, Laurent; Mazzanti, Marinella
Assembling Diuranium Complexes in Different States of Charge with a Bridging Redox-Active Ligand
Chemical Science, 2022
1567556 CIFC96 H226 K2 N14 O16 Si12 U2P -113.7816; 16.73893; 17.0063
63.8536; 84.3138; 74.6504
3395.39Modder, dieuwertje; Batov, Mikhail; Rajeshkumar, Thayalan; Scopelliti, Rosario; Zivkovic, Ivica; Sienkiewicz, Andrzej; Maron, Laurent; Mazzanti, Marinella
Assembling Diuranium Complexes in Different States of Charge with a Bridging Redox-Active Ligand
Chemical Science, 2022
1567557 CIFC71 H141 B N10 Si12 U2P -115.1222; 15.2178; 23.8147
98.8987; 91.1267; 92.6498
5406.64Modder, dieuwertje; Batov, Mikhail; Rajeshkumar, Thayalan; Scopelliti, Rosario; Zivkovic, Ivica; Sienkiewicz, Andrzej; Maron, Laurent; Mazzanti, Marinella
Assembling Diuranium Complexes in Different States of Charge with a Bridging Redox-Active Ligand
Chemical Science, 2022
1567558 CIFC60 H78 N8 O24 Zn7P -3 c 114.068; 14.068; 23.3614
90; 90; 120
4004Li, Tian; Wang, Yi-Fan; Yin, Zheng; Li, Jian; Peng, Xu; Zeng, Ming-Hua
The sequential structural transformation of a heptanuclear zinc cluster towards hierarchical porous carbon for supercapacitor applications
Chemical Science, 2022
1567559 CIFC18 H11 F3 N2P 1 21/n 111.3732; 7.0194; 17.8991
90; 100.777; 90
1403.74Huang, Mengjun; Ma, Jiawei; Zou, Zhenlei; Li, Heyin; Liu, Jiyang; Kong, Lingyu; Pan, Yi; Zhang, Weigang; Liang, Yong; Wang, Yi
A photoinduced transient activating strategy for late-stage chemoselective C(sp3)–H trifluoromethylation of azines
Chemical Science, 2022
1567560 CIFC8 H5 F3 N2 O2 SP 1 21/c 110.81; 5.693; 16.013
90; 93.45; 90
983.7Huang, Mengjun; Ma, Jiawei; Zou, Zhenlei; Li, Heyin; Liu, Jiyang; Kong, Lingyu; Pan, Yi; Zhang, Weigang; Liang, Yong; Wang, Yi
A photoinduced transient activating strategy for late-stage chemoselective C(sp3)–H trifluoromethylation of azines
Chemical Science, 2022
1567561 CIFC21 H19 F3 N2 OP 1 21/n 18.832; 11.476; 17.721
90; 91.06; 90
1795.8Huang, Mengjun; Ma, Jiawei; Zou, Zhenlei; Li, Heyin; Liu, Jiyang; Kong, Lingyu; Pan, Yi; Zhang, Weigang; Liang, Yong; Wang, Yi
A photoinduced transient activating strategy for late-stage chemoselective C(sp3)–H trifluoromethylation of azines
Chemical Science, 2022
1567562 CIFC49 H46 B2 F8 N4 O P2 RuP 1 21/c 110.0485; 17.8373; 26.9426
90; 98.285; 90
4778.7Gong, Huihua; Cui, Tianhua; Liu, Zheyuan; Zheng, Yanling; Zheng, Xueli; Fu, Haiyan; Yuan, Maolin; Chen, Hua; Xu, Jiaqi; Li, Ruixiang
Nitrogen–nitrogen-functionalized N-heterocyclic carbene ruthenium(ii) complexes realized efficient CO2 hydrogenation to formate
Catalysis Science & Technology, 2022, 12, 6213-6218
1567563 CIFC32 H34 B F4 N4 O P RuP 1 21/n 117.8555; 10.37049; 18.2838
90; 110.261; 90
3176.13Gong, Huihua; Cui, Tianhua; Liu, Zheyuan; Zheng, Yanling; Zheng, Xueli; Fu, Haiyan; Yuan, Maolin; Chen, Hua; Xu, Jiaqi; Li, Ruixiang
Nitrogen–nitrogen-functionalized N-heterocyclic carbene ruthenium(ii) complexes realized efficient CO2 hydrogenation to formate
Catalysis Science & Technology, 2022, 12, 6213-6218
1567564 CIFC31 H32 Cl N4 O P RuP -117.5755; 19.7613; 21.9822
106.12; 103.92; 103.786
6727.3Gong, Huihua; Cui, Tianhua; Liu, Zheyuan; Zheng, Yanling; Zheng, Xueli; Fu, Haiyan; Yuan, Maolin; Chen, Hua; Xu, Jiaqi; Li, Ruixiang
Nitrogen–nitrogen-functionalized N-heterocyclic carbene ruthenium(ii) complexes realized efficient CO2 hydrogenation to formate
Catalysis Science & Technology, 2022, 12, 6213-6218
1567565 CIFC62 H101 Cl N4 O5 UP 21 21 2115.083; 17.018; 24.513
90; 90; 90
6292Löffler, Sascha T.; Hümmer, Julian; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Unprecedented pairs of uranium (iv/v) hydroxido and (iv/v/vi) oxido complexes supported by a seven-coordinate cyclen-anchored tris-aryloxide ligand
Chemical Science, 2022
1567566 CIFC62 H105 F N4 O5 UP 1 21/c 117.1229; 13.5864; 27.4309
90; 100.063; 90
6283.3Löffler, Sascha T.; Hümmer, Julian; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Unprecedented pairs of uranium (iv/v) hydroxido and (iv/v/vi) oxido complexes supported by a seven-coordinate cyclen-anchored tris-aryloxide ligand
Chemical Science, 2022
1567567 CIFC62 H105 F1.79 N4 O5 UP 1 21/n 113.5741; 15.3727; 30.4035
90; 102.168; 90
6201.8Löffler, Sascha T.; Hümmer, Julian; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Unprecedented pairs of uranium (iv/v) hydroxido and (iv/v/vi) oxido complexes supported by a seven-coordinate cyclen-anchored tris-aryloxide ligand
Chemical Science, 2022
1567568 CIFC62 H102 N4 O6 UP 1 21/n 110.7445; 16.3263; 37.618
90; 90.093; 90
6598.9Löffler, Sascha T.; Hümmer, Julian; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Unprecedented pairs of uranium (iv/v) hydroxido and (iv/v/vi) oxido complexes supported by a seven-coordinate cyclen-anchored tris-aryloxide ligand
Chemical Science, 2022
1567569 CIFC75 H107 F6 N4 O4 Sb UP 1 2/c 123.6848; 12.0981; 27.9247
90; 113.046; 90
7363Löffler, Sascha T.; Hümmer, Julian; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Unprecedented pairs of uranium (iv/v) hydroxido and (iv/v/vi) oxido complexes supported by a seven-coordinate cyclen-anchored tris-aryloxide ligand
Chemical Science, 2022
1567570 CIFC60 H97 N4 O5.5 UC 1 2/c 130.404; 10.566; 37.842
90; 106.97; 90
11627Löffler, Sascha T.; Hümmer, Julian; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Unprecedented pairs of uranium (iv/v) hydroxido and (iv/v/vi) oxido complexes supported by a seven-coordinate cyclen-anchored tris-aryloxide ligand
Chemical Science, 2022
1567571 CIFC75 H106 F6 N4 O4 Sb UP 1 2/c 123.6833; 12.0691; 27.9262
90; 113.169; 90
7338.5Löffler, Sascha T.; Hümmer, Julian; Scheurer, Andreas; Heinemann, Frank W.; Meyer, Karsten
Unprecedented pairs of uranium (iv/v) hydroxido and (iv/v/vi) oxido complexes supported by a seven-coordinate cyclen-anchored tris-aryloxide ligand
Chemical Science, 2022
1567572 CIFC44 H40 Br4 Co2 N4 O6P -19.4017; 10.5681; 12.696
66.4289; 77.1738; 84.9305
1127.35Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567573 CIFC31 H44 Co N3 O2P 1 21/c 111.59303; 11.77994; 21.25835
90; 91.1883; 90
2902.53Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567574 CIFC68 H68 Co2 N4 O6P b c a10.9817; 17.1391; 31.4588
90; 90; 90
5921.1Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567575 CIFC84 H100 Co2 N4 O6P -111.1838; 12.1674; 15.6011
72.164; 70.4512; 89.2308
1895.03Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567576 CIFC52 H60 Co2 N4 O6P -111.1341; 13.1609; 17.4589
81.674; 71.6133; 84.1723
2397.89Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567577 CIFC57 H72 Co2 N4 O10P 1 21/c 114.3182; 12.0109; 15.9104
90; 97.507; 90
2712.73Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567578 CIFC60 H80 Co2 N8 O6P -113.2692; 15.2605; 16.5352
77.6834; 76.0242; 66.204
2947.53Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567579 CIFC54 H58 Co2 N4 O6P 1 21/c 113.5589; 35.2233; 16.1183
90; 105.07; 90
7433.2Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567580 CIFC53 H76 N2 OP -114.2247; 18.7107; 19.0753
109.83; 93.98; 103.16
4590.5Théry, Valentin; Molton, Florian; Sirach, Selim; Tillet, Neven; Pécaut, Jacques; Tomás-Mendivil, Eder; Martin, David
The curious case of a sterically crowded Stenhouse salt
Chemical Science, 2022, 13, 9755-9760
1567581 CIFC53 H79 Cl N2 O2P 1 21/c 113.0058; 18.6532; 20.2559
90; 107.607; 90
4683.9Théry, Valentin; Molton, Florian; Sirach, Selim; Tillet, Neven; Pécaut, Jacques; Tomás-Mendivil, Eder; Martin, David
The curious case of a sterically crowded Stenhouse salt
Chemical Science, 2022, 13, 9755-9760
1567582 CIFC57 H84 F3 N2 O4.5 SI 1 2/a 117.3378; 16.0403; 38.924
90; 95.096; 90
10782.1Théry, Valentin; Molton, Florian; Sirach, Selim; Tillet, Neven; Pécaut, Jacques; Tomás-Mendivil, Eder; Martin, David
The curious case of a sterically crowded Stenhouse salt
Chemical Science, 2022, 13, 9755-9760
1567583 CIFC54 H78 Cl2 F12 N2 O P2P 1 21/n 112.152; 31.9515; 14.2567
90; 97.129; 90
5492.7Théry, Valentin; Molton, Florian; Sirach, Selim; Tillet, Neven; Pécaut, Jacques; Tomás-Mendivil, Eder; Martin, David
The curious case of a sterically crowded Stenhouse salt
Chemical Science, 2022, 13, 9755-9760
1567584 CIFC69 H63 F18 N8 P3P n a 2120.9197; 14.8105; 21.4828
90; 90; 90
6656.04La Cognata, Sonia; Armentano, Donatella; Marchesi, Nicoletta; Grisoli, Pietro; Pascale, Alessia; Kieffer, Marion; Taglietti, Angelo; Davis, Anthony P.; Amendola, Valeria
A Benzimidazolium-Based Organic Cage with Antimicrobial Activity
Chemistry, 2022, 4, 855-864
1567585 CIFC68 H48 Co N10 S2P 1 21/c 18.7148; 18.4121; 18.2547
90; 101.524; 90
2870.06Rocco, Dalila; Nikoletić, Anamarija; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
To Be or Not to Be a (4,4) Net: Reactions of 4′-{4-(N,N-Diethylaminophenyl)}- and 4′-{4-(N,N-Diphenylaminophenyl)}-3,2′:6′,3″- and 4,2′:6′,4″-Terpyridines with Cobalt(II) Thiocyanate
Crystals, 2022, 12, 1136
1567586 CIFC54 H50 Cl6 Co N10 S2P 1 21/n 18.3422; 16.5164; 19.9774
90; 100.072; 90
2710.13Rocco, Dalila; Nikoletić, Anamarija; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
To Be or Not to Be a (4,4) Net: Reactions of 4′-{4-(N,N-Diethylaminophenyl)}- and 4′-{4-(N,N-Diphenylaminophenyl)}-3,2′:6′,3″- and 4,2′:6′,4″-Terpyridines with Cobalt(II) Thiocyanate
Crystals, 2022, 12, 1136
1567587 CIFC73 H59 Cl9 Co N10 O2 S2P 1 21/c 114.7142; 9.842; 25.64
90; 94.944; 90
3699.3Rocco, Dalila; Nikoletić, Anamarija; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
To Be or Not to Be a (4,4) Net: Reactions of 4′-{4-(N,N-Diethylaminophenyl)}- and 4′-{4-(N,N-Diphenylaminophenyl)}-3,2′:6′,3″- and 4,2′:6′,4″-Terpyridines with Cobalt(II) Thiocyanate
Crystals, 2022, 12, 1136
1567588 CIFC52.8 H48.8 Cl2.4 Co N10 S2P 1 21/n 113.3183; 12.5045; 15.2418
90; 96.533; 90
2521.87Rocco, Dalila; Nikoletić, Anamarija; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
To Be or Not to Be a (4,4) Net: Reactions of 4′-{4-(N,N-Diethylaminophenyl)}- and 4′-{4-(N,N-Diphenylaminophenyl)}-3,2′:6′,3″- and 4,2′:6′,4″-Terpyridines with Cobalt(II) Thiocyanate
Crystals, 2022, 12, 1136
1567589 CIFC33 H24 N4C 1 2/c 134.855; 8.6116; 30.178
90; 146.585; 90
4988.3Rocco, Dalila; Nikoletić, Anamarija; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
To Be or Not to Be a (4,4) Net: Reactions of 4′-{4-(N,N-Diethylaminophenyl)}- and 4′-{4-(N,N-Diphenylaminophenyl)}-3,2′:6′,3″- and 4,2′:6′,4″-Terpyridines with Cobalt(II) Thiocyanate
Crystals, 2022, 12, 1136
1567590 CIFC30 H20 Cl6 O PP -110.0941; 10.4249; 15.3161
73.955; 87.469; 73.633
1485.17Xu, Shibo; Nishimura, Kazutoshi; Saito, Kosuke; Hirano, Koji; Miura, Masahiro
Palladium-catalysed C–H arylation of benzophospholes with aryl halides
Chemical Science, 2022
1567591 CIFC22 H19 O PP 1 21/c 112.5743; 11.368; 11.7601
90; 93.369; 90
1678.14Xu, Shibo; Nishimura, Kazutoshi; Saito, Kosuke; Hirano, Koji; Miura, Masahiro
Palladium-catalysed C–H arylation of benzophospholes with aryl halides
Chemical Science, 2022
1567592 CIFC68 H114 Ag20 F24 N4 O18 S11P 1 21/n 116.3357; 16.1055; 23.5813
90; 94.397; 90
6185.9Mandal, Sukhendu; Biswas, Sourav; Das, Anish Kumar; Manna, Surya Sekhar; Pathak, Biswarup
Template-Assisted Alloying of Atom-Precise Silver Nanocluster: A New Approach to Generate Cluster Functionality
Chemical Science, 2022
1567593 CIFC162 H288 Ag40 Cu2 F48 N12 O48 S23P 1 21/n 115.9453; 18.304; 24.394
90; 105.548; 90
6859.2Mandal, Sukhendu; Biswas, Sourav; Das, Anish Kumar; Manna, Surya Sekhar; Pathak, Biswarup
Template-Assisted Alloying of Atom-Precise Silver Nanocluster: A New Approach to Generate Cluster Functionality
Chemical Science, 2022
1567594 CIFC69 H118 Ag20 Cu0 F24 N4 O24 S10P 1 21/c 115.4136; 30.794; 28.051
90; 103.798; 90
12930Mandal, Sukhendu; Biswas, Sourav; Das, Anish Kumar; Manna, Surya Sekhar; Pathak, Biswarup
Template-Assisted Alloying of Atom-Precise Silver Nanocluster: A New Approach to Generate Cluster Functionality
Chemical Science, 2022
1567595 CIFC79 H77 Ni3 O P6 SnP -115.7957; 15.853; 15.9408
88.234; 74.099; 85.076
3824.7Torquato, Nicole A.; Mrse, Anthony A.; Gembicky, Milan; Chan, Thomas; Brunner, Felix M.; Kubiak, Clifford P.; Bertrand, Quentin C.; Palasz, Joseph M.
Synthesis, Structure and Reactivity of µ3-SnH Capped Trinuclear Nickel Cluster
Chemical Science, 2022
1567596 CIFC81 H80 Br Ni3 O P6 SnP -112.692; 13.093; 24.4579
90.583; 102.885; 112.374
3643.3Torquato, Nicole A.; Mrse, Anthony A.; Gembicky, Milan; Chan, Thomas; Brunner, Felix M.; Kubiak, Clifford P.; Bertrand, Quentin C.; Palasz, Joseph M.
Synthesis, Structure and Reactivity of µ3-SnH Capped Trinuclear Nickel Cluster
Chemical Science, 2022
1567597 CIFC81 H78 Ni3 P6 SnP -111.9779; 13.7494; 23.0279
91.234; 101.72; 107.029
3537.25Torquato, Nicole A.; Mrse, Anthony A.; Gembicky, Milan; Chan, Thomas; Brunner, Felix M.; Kubiak, Clifford P.; Bertrand, Quentin C.; Palasz, Joseph M.
Synthesis, Structure and Reactivity of µ3-SnH Capped Trinuclear Nickel Cluster
Chemical Science, 2022
1567598 CIFC83 H77 I Ni3 P6 SnP 1 21/c 116.0909; 22.5824; 20.2582
90; 103.455; 90
7159.2Torquato, Nicole A.; Mrse, Anthony A.; Gembicky, Milan; Chan, Thomas; Brunner, Felix M.; Kubiak, Clifford P.; Bertrand, Quentin C.; Palasz, Joseph M.
Synthesis, Structure and Reactivity of µ3-SnH Capped Trinuclear Nickel Cluster
Chemical Science, 2022
1567599 CIFC16 H20 Cl N3 SP 1 21/c 111.6247; 17.1959; 8.2511
90; 109.867; 90
1551.21Pivovarova, Ekaterina; Climova, Alina; Świątkowski, Marcin; Staszewski, Marek; Walczyński, Krzysztof; Dzięgielewski, Marek; Bauer, Marta; Kamysz, Wojciech; Krześlak, Anna; Jóźwiak, Paweł; Czylkowska, Agnieszka
Synthesis and Biological Evaluation of Thiazole-Based Derivatives with Potential against Breast Cancer and Antimicrobial Agents
International Journal of Molecular Sciences, 2022, 23, 9844
1567600 CIFC42 H52 B2 O2P 1 21 111.49; 7.2911; 20.791
90; 93.2; 90
1739Sirin-Sariaslan, Ayla; Naumann, Stefan
Chiral diboranes as catalysts for the stereoselective organopolymerization of epoxides
Chemical Science, 2022
1567601 CIFC60 H68 Ga N4 PP 1 21/n 111.5827; 15.4151; 27.061
90; 90.708; 90
4831.3Sigmund, Lukas M.; Engels, Eliane; Richert, Nick; Greb, Lutz
Calix[4]pyrrolato gallate: square planar-coordinated gallium(iii) and its metal–ligand cooperative reactivity with CO2 and alcohols
Chemical Science, 2022, 13, 11215-11220
1567602 CIFC52.5 H53 Cl Ga N4 PP 1 21/c 125.411; 16.6359; 23.7139
90; 107.797; 90
9545Sigmund, Lukas M.; Engels, Eliane; Richert, Nick; Greb, Lutz
Calix[4]pyrrolato gallate: square planar-coordinated gallium(iii) and its metal–ligand cooperative reactivity with CO2 and alcohols
Chemical Science, 2022, 13, 11215-11220
1567603 CIFC56 H60 Ga N4 O PP 1 21/c 113.0677; 21.406; 17.1423
90; 108.63; 90
4543.9Sigmund, Lukas M.; Engels, Eliane; Richert, Nick; Greb, Lutz
Calix[4]pyrrolato gallate: square planar-coordinated gallium(iii) and its metal–ligand cooperative reactivity with CO2 and alcohols
Chemical Science, 2022, 13, 11215-11220
1567604 CIFC59.33333 H43.33333 Cl4 FeP 1 21/c 113.9204; 26.8345; 18.8544
90; 97.032; 90
6990Kwon, Hyejin; Newell, Brian S.; Bruns, Carson J.
Redox-Switchable Host-Guest Complexes of Metallocenes and [8]Cycloparaphenylene
Nanoscale, 2022
1567605 CIFC58 H42 Co F12 P2C 1 2/c 138.1212; 13.7764; 24.9606
90; 129.152; 90
10165.4Kwon, Hyejin; Newell, Brian S.; Bruns, Carson J.
Redox-Switchable Host-Guest Complexes of Metallocenes and [8]Cycloparaphenylene
Nanoscale, 2022
1567606 CIF
HKL
Paper
C25 H20 F7 N3 O2P 1 21/n 112.1592; 18.926; 20.3097
90; 91.474; 90
4672.2Shimazaki, Runa; Sadakiyo, Masaaki
Ethidium heptafluorobutyrate
IUCrData, 2022, 7, x220884
1567607 CIF
HKL
Paper
C4 H6 Cl N3 O2P 1 21/c 16.3498; 9.8991; 11.5969
90; 105.817; 90
701.35Bellia, Sophia; Anderson, Grace; Zeller, Matthias; Mirjafari, Arsalan; Hillesheim, Patrick C.
1-Methyl-5-nitroimidazolium chloride
IUCrData, 2022, 7, x220878
1567608 CIFC23 H29 NP 1 21 110.9102; 6.1038; 14.7452
90; 99.5; 90
968.47Sun, Yue; Ma, Chun; Li, Zhiming; Zhang, Junliang
Palladium/GF-Phos-catalyzed asymmetric carbenylative amination to access chiral pyrrolidines and piperidines
Chemical Science, 2022, 13, 11150-11155
1567609 CIFC23 H16 I3 NP b c n21.1343; 13.7339; 7.328
90; 90; 90
2127Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567610 CIFC22 H14 I3 NP -18.0838; 11.8898; 12.2871
64.355; 77.901; 77.39
1030.02Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567611 CIFC23 H14 F3 I2 N O3 SP -18.5783; 11.1636; 13.3063
74.307; 71.324; 79.269
1155.23Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567612 CIFC22 H15 I3 N2P b c n21.0883; 13.773; 7.3022
90; 90; 90
2120.9Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567613 CIFC22 H14 I3 NP b c n21.0383; 13.782; 7.3031
90; 90; 90
2117.5Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567614 CIFC24 H16 F3 I2 N O3 SP -17.2077; 12.3954; 14.0967
98.565; 101.823; 91.413
1216.98Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567615 CIFC23 H14 F3 I2 N O3 SP -17.1362; 12.3559; 14.2656
98.46; 103.067; 94.936
1202.63Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567616 CIFC23 H15 F3 I2 N2 O3 SP -4 21 c22.544; 22.544; 9.5927
90; 90; 90
4875.3Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567617 CIFC59 H51 F6 N5 O6 S2C 1 2/c 122.116; 17.029; 16.379
90; 124.27; 90
5098Karak, Pirudhan; Choudhury, Joyanta
Conformationally flexible heterohelicenes as stimuli-controlled soft molecular springs
Chemical Science, 2022, 13, 11163-11173
1567618 CIFC51 H45 N5P 1 21/n 18.4766; 15.6816; 28.099
90; 95.655; 90
3716.9Karak, Pirudhan; Choudhury, Joyanta
Conformationally flexible heterohelicenes as stimuli-controlled soft molecular springs
Chemical Science, 2022, 13, 11163-11173
1567619 CIFC57 H49 Cl4 N5P 1 21/n 117.0926; 16.467; 17.5046
90; 113.674; 90
4512.3Karak, Pirudhan; Choudhury, Joyanta
Conformationally flexible heterohelicenes as stimuli-controlled soft molecular springs
Chemical Science, 2022, 13, 11163-11173
1567620 CIFC59 H55 Cl6 I2 N5 Rh2C 1 2/c 115.6999; 18.4945; 20.4988
90; 91.779; 90
5949.2Karak, Pirudhan; Choudhury, Joyanta
Conformationally flexible heterohelicenes as stimuli-controlled soft molecular springs
Chemical Science, 2022, 13, 11163-11173
1567621 CIFC57 H55 Cl2 F6 N5 O6 S2P 1 21/c 116.175; 18.4493; 18.016
90; 102.497; 90
5248.9Karak, Pirudhan; Choudhury, Joyanta
Conformationally flexible heterohelicenes as stimuli-controlled soft molecular springs
Chemical Science, 2022, 13, 11163-11173
1567622 CIFC18 H21 N O6P -18.1602; 10.1021; 11.5212
88.2151; 69.4794; 72.0806
843.2Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567623 CIFC16 H17 N O6P 1 21/c 112.998; 7.7936; 15.3862
90; 106.506; 90
1494.41Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567624 CIFC18 H21 N O6C 1 c 15.03; 20.5537; 16.8829
90; 97.379; 90
1730.99Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567625 CIFC18 H21 N O6P 1 21/c 117.15; 9.733; 10.702
90; 106.541; 90
1712.5Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567626 CIFC16 H17 N O6P 1 21/c 18.1387; 24.2934; 8.5069
90; 117.414; 90
1493.08Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567627 CIFC16 H17 N O6P 1 21/n 17.8712; 16.4752; 11.757
90; 91.5968; 90
1524.05Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567628 CIFC64 H66 Si2P 1 21/n 118.2848; 7.9227; 19.28
90; 117.08; 90
2486.81Zong, Chaoyang; Yang, Shuyuan; Sun, Yajing; Zhang, Lifeng; Hu, Jinlian; Hu, Wenping; Li, Rongjin; Sun, Zhe
Isomeric Dibenzooctazethrene Diradicals for High-Performance Air-Stable Organic Field-Effect Transistors
Chemical Science, 2022
1567629 CIFC64 H66 Si2P -17.9997; 8.8382; 17.8954
94.227; 96.681; 94.149
1249.06Zong, Chaoyang; Yang, Shuyuan; Sun, Yajing; Zhang, Lifeng; Hu, Jinlian; Hu, Wenping; Li, Rongjin; Sun, Zhe
Isomeric Dibenzooctazethrene Diradicals for High-Performance Air-Stable Organic Field-Effect Transistors
Chemical Science, 2022
1567630 CIFC22 H13 F2 N OC 1 2/c 124.1916; 9.9649; 14.5436
90; 112.784; 90
3232.4Wang, Gang; Li, Wenqi; Liu, Tianxiang; Zhang, Yonghong; Wang, Bin; Xue, Fei; Jin, Weiwei; Ma, Caiyan; Xia, Yu; Liu, Chenjiang
Palladium-catalyzed intramolecular Heck dearomative <i>gem</i>-difluorovinylation of indoles.
Chemical science, 2022, 13, 11594-11599
1567631 CIFC17 H11 F2 N OP 1 21/n 113.16; 7.282; 14.2
90; 99.631; 90
1341.6Wang, Gang; Li, Wenqi; Liu, Tianxiang; Zhang, Yonghong; Wang, Bin; Xue, Fei; Jin, Weiwei; Ma, Caiyan; Xia, Yu; Liu, Chenjiang
Palladium-catalyzed intramolecular Heck dearomative <i>gem</i>-difluorovinylation of indoles.
Chemical science, 2022, 13, 11594-11599
1567632 CIFC25 H30 N2 O2P -4 21 c20.192; 20.192; 11.043
90; 90; 90
4502.4Wang, Gang; Li, Wenqi; Liu, Tianxiang; Zhang, Yonghong; Wang, Bin; Xue, Fei; Jin, Weiwei; Ma, Caiyan; Xia, Yu; Liu, Chenjiang
Palladium-catalyzed intramolecular Heck dearomative <i>gem</i>-difluorovinylation of indoles.
Chemical science, 2022, 13, 11594-11599
1567633 CIFC96 H85 N3 O4 S2P 1 21/c 120.891; 8.271; 44.433
90; 102.813; 90
7486Zhu, Jiangyu; Li, Wenhao; Zhang, Ning; An, Dongyue; Zhao, Yan; Lu, Xuefeng; Liu, Yunqi
Size-dependent properties and unusual reactivity of novel nonplanar heterocycloarenes
Chemical Science, 2022, 13, 11174-11182
1567634 CIFC80 H48 Cl6 N2 O8 S2P -112.745; 14.782; 19.522
82.434; 83.954; 80.211
3579.8Zhu, Jiangyu; Li, Wenhao; Zhang, Ning; An, Dongyue; Zhao, Yan; Lu, Xuefeng; Liu, Yunqi
Size-dependent properties and unusual reactivity of novel nonplanar heterocycloarenes
Chemical Science, 2022, 13, 11174-11182
1567635 CIFC24.24 H31.47 N3.18 O7.38 Zn2P 31 2 121.5982; 21.5982; 6.9071
90; 90; 120
2790.4Siegelman, Rebecca L.; Thompson, Joshua A.; Mason, Jarad; McDonald, Thomas M.; Long, Jeffrey R.
A cooperative adsorbent for the switch-like capture of carbon dioxide from crude natural gas
Chemical Science, 2022
1567636 CIFC17 H19 N O SP 1 21 18.8663; 8.793; 10.1594
90; 108.871; 90
749.5Zhang, Jian-Xin; Yang, Peng-Fei; Shu, Wei
Access to Dialkylated Allylic Stereogenic Centers by Ni-Catalysed Enantioselective Hydrovinylation of Unactivated Alkenes
Chemical Science, 2022
1567637 CIFC20 H27 N O2P 1 21/c 16.3182; 39.6141; 7.7124
90; 111.769; 90
1792.68Cooper, Phillippa; Dalling, Andrew G.; Farrar, Elliot H. E.; Aldhous, Timothy P.; Grélaud, Simon; Lester, Eleanor; Feron, Lyman J.; Kemmitt, Paul D.; Grayson, Matthew N.; Bower, John F.
Atom and step economical synthesis of acyclic quaternary centers via iridium-catalyzed hydroarylative cross-coupling of 1,1-disubstituted alkenes
Chemical Science, 2022, 13, 11183-11189
1567638 CIF
HKL
Paper
C21 H18 O4P -18.3312; 9.6506; 11.797
94.261; 107.335; 112.326
818.4Sung, Jiha
3-(2,3-Dimethoxyphenyl)-2,3-dihydro-1<i>H</i>-benzo[<i>f</i>]chromen-1-one
IUCrData, 2022, 7, x220885
1567639 CIF
HKL
Paper
C20 H14 I2 N2 O2P b c a7.4776; 19.104; 26.0919
90; 90; 90
3727.28Blackwelder, Lauren A.; Kelley, Andrea R.; Balaich, Gary J.; Jefferies, Latisha R.
2,2'-{(1<i>E</i>,1'<i>E</i>)-[Ethane-1,2-diylbis(azanylylidene)]bis(methanylylidene)}bis(4-iodophenol)
IUCrData, 2022, 7, x220895
1567640 CIFC160 H204 N84 O72 Pd6P -3 c 127.653; 27.653; 44.488
90; 90; 120
29462Chakraborty, Debsena; Saha, Rupak; Clegg, Jack Kay; Mukherjee, Partha Sarathi
Selective separation of planar and non-planar hydrocarbons using an aqueous Pd6 interlocked cage
Chemical Science, 2022
1567641 CIFC21 H29 Br O4P -16.36017; 7.8529; 20.1551
91.523; 91.016; 93.88
1003.81Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567642 CIFC21 H29 Br O4P b c a10.6941; 8.218; 46.3766
90; 90; 90
4075.8Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567643 CIFC21 H29 Br O4P -16.41587; 12.0405; 13.3039
94.139; 91.6023; 101.288
1004.29Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567644 CIFC14 H26 O3P 1 21/n 15.8614; 15.5412; 14.8746
90; 90.764; 90
1354.85Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567645 CIFC21 H29 Br O4P 1 21/c 114.0432; 7.0309; 21.1186
90; 100.447; 90
2050.61Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567646 CIFC35 H38 O4P -16.28197; 12.2599; 19.1503
89.562; 87.114; 78.209
1441.93Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567647 CIFC21 H29 Br O4P -17.44418; 11.53654; 12.84945
69.1422; 81.678; 84.3027
1018.98Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567648 CIFC25 H25 N O3P 1 21 110.5777; 41.8595; 10.6059
90; 115.198; 90
4249.18Guo, Wengang; Jiang, Feng; Li, Shijia; Sun, Jianwei
Organocatalytic asymmetric azidation of sulfoxonium ylides: mild synthesis of enantioenriched α-azido ketones bearing a labile tertiary stereocenter.
Chemical science, 2022, 13, 11648-11655
1567649 CIFC24 H48 Cl2 Cr2 Si4P 1 21/c 113.2426; 7.9314; 15.6465
90; 101.402; 90
1610.96Trummer, David; Nobile, Anna Giorgia; Payard, Pierre-Adrien; Ashuiev, Anton; Kakiuchi, Yuya; Klose, Daniel; Jeschke, Gunnar; Copéret, Christophe
Union carbide polymerization catalysts: from uncovering active site structures to designing molecularly-defined analogs
Chemical Science, 2022, 13, 11091-11098
1567650 CIFC26 H36 CrP 1 21/n 19.3657; 16.7589; 14.5402
90; 105.649; 90
2197.6Trummer, David; Nobile, Anna Giorgia; Payard, Pierre-Adrien; Ashuiev, Anton; Kakiuchi, Yuya; Klose, Daniel; Jeschke, Gunnar; Copéret, Christophe
Union carbide polymerization catalysts: from uncovering active site structures to designing molecularly-defined analogs
Chemical Science, 2022, 13, 11091-11098
1567651 CIF
HKL
Paper
C10 H13 N O2P -18.405; 11.029; 11.52
89.1; 77.06; 87.17
1039.5Priyanka, Prabhakar; Jayanna, Bidarur K.; Kiran Kumar, Haruvegowda; Yathirajan, Hemmige S.; Divakara, Thayamma R.; Foro, Sabine; Butcher, Ray J.
Isopropyl 4-aminobenzoate
IUCrData, 2022, 7, x220904
1567652 CIFC29.5 H31 Cl N2I 1 2/a 122.0567; 7.5133; 32.5379
90; 109.612; 90
5079.32Cui, Xian-Chao; Zhang, Hu; Wang, Yi-Ping; Qu, Jian-Ping; Kang, Yan-Biao
Synthesis of carbinoxamine via α-C(sp3)–H 2-pyridylation of O, S or N-containing compounds enabled by non-D–A-type super organoreductants and sulfoxide- or sulfide HAT reagents
Chemical Science, 2022, 13, 11246-11251
1567653 CIFC27 H26 N2 OP -17.8864; 9.9577; 15.3148
75.304; 85.678; 67.535
1074.74Cui, Xian-Chao; Zhang, Hu; Wang, Yi-Ping; Qu, Jian-Ping; Kang, Yan-Biao
Synthesis of carbinoxamine via α-C(sp3)–H 2-pyridylation of O, S or N-containing compounds enabled by non-D–A-type super organoreductants and sulfoxide- or sulfide HAT reagents
Chemical Science, 2022, 13, 11246-11251
1567654 CIFC21 H16 Cl NP 1 21/n 110.7317; 5.511; 27.4878
90; 99.361; 90
1604.05Li, Quanzhe; Gu, Xintao; Wei, Yin; Shi, Min
Visible-light-induced indole synthesis <i>via</i> intramolecular C-N bond formation: desulfonylative C(sp<sup>2</sup>)-H functionalization.
Chemical science, 2022, 13, 11623-11632
1567655 CIFC24 H28 Br4 N4 O4I 1 2/a 120.6359; 5.1809; 27.7349
90; 104.528; 90
2870.4Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567656 CIFC18 H14 I4 N2 O4P 1 21/c 114.0017; 8.2362; 19.1456
90; 104.636; 90
2136.24Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567657 CIFC14 H8 I4 N8P -111.9316; 12.2715; 15.2444
73.159; 73.857; 79.026
2037.41Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567658 CIFC26 H34 N2 O4 S4P -17.2152; 8.0923; 12.5451
87.957; 82.964; 66.841
668.32Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567659 CIFC24 H30 F2 N4 O4P -110.1072; 11.4012; 11.5402
94.868; 95.841; 112.726
1208.99Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567660 CIFC16 H18 N2 Se4P 1 2/n 115.5783; 7.9499; 29.5587
90; 90.3204; 90
3660.67Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567661 CIFC22 H26 N2 O4 Se4P b c n16.0349; 15.8463; 19.0464
90; 90; 90
4839.57Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567662 CIFC16 H18 N2 S4P 1 2/n 115.105; 7.8801; 28.9196
90; 90.6804; 90
3442.03Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567663 CIFC14 H12 F2 N2 Te2P 1 21/n 16.4567; 8.6728; 13.3795
90; 92.32; 90
748.61Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567664 CIFC16 H18 N2 Te4P 1 21 110.7335; 10.5743; 18.0208
90; 95.2723; 90
2036.69Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567665 CIFC34 H44 Br0 N4 O4P -14.7183; 12.508; 13.014
78.569; 86.876; 82.105
745.4Bansal, Deepak; Kundu, Arup; Singh, Vijay Pal; Pal, Arun K.; Datta, Ayan; Dasgupta, Jyotishman; Mukhopadhyay, Pritam
A highly contorted push-pull naphthalenediimide dimer and evidence of intramolecular singlet exciton fission.
Chemical science, 2022, 13, 11506-11512
1567666 CIFC56 H64 N8 O8P 43 21 214.7104; 14.7104; 23.995
90; 90; 90
5192.4Bansal, Deepak; Kundu, Arup; Singh, Vijay Pal; Pal, Arun K.; Datta, Ayan; Dasgupta, Jyotishman; Mukhopadhyay, Pritam
A highly contorted push-pull naphthalenediimide dimer and evidence of intramolecular singlet exciton fission.
Chemical science, 2022, 13, 11506-11512
1567667 CIFCd S4 Si SrA m a 210.2821; 10.1551; 6.3699
90; 90; 90
665.12Yang, He-Di; Ran, Mao-Yin; Zhou, Sheng-Hua; Wu, Xin-Tao; Lin, Hua; Zhu, Qi-Long
Rational design via dual-site aliovalent substitution leads to an outstanding IR nonlinear optical material with well-balanced comprehensive properties
Chemical Science, 2022, 13, 10725-10733
1567668 CIFGa2 S4 SrF d d d :212.2216; 20.5008; 20.8426
90; 90; 90
5222.2Yang, He-Di; Ran, Mao-Yin; Zhou, Sheng-Hua; Wu, Xin-Tao; Lin, Hua; Zhu, Qi-Long
Rational design via dual-site aliovalent substitution leads to an outstanding IR nonlinear optical material with well-balanced comprehensive properties
Chemical Science, 2022, 13, 10725-10733
1567669 CIFC74 H44 F4 N8 O3 S5C 1 2/c 123.7933; 57.27; 13.4957
90; 109.688; 90
17314.8Luo, Zhenghui; Gao, Yuan; Lai, Hanjian; Li, Yuxiang; Wu, Ziang; Chen, Zhanxiang; Sun, Rui; Ren, Jiaqi; Zhang, Cai’e; He, Feng; Woo, HanYoung; Min, Jie; Yang, Chuluo
Asymmetric side-chain substitution enables a 3D network acceptor with hydrogen bond assisted crystal packing and enhanced electronic coupling for efficient organic solar cells
Energy & Environmental Science, 2022, 15, 4601-4611
1567670 CIFC58 H44 F0.5 N16 O4.5 S5P -113.457; 23.14; 30.127
70.475; 86.756; 80.476
8720Luo, Zhenghui; Gao, Yuan; Lai, Hanjian; Li, Yuxiang; Wu, Ziang; Chen, Zhanxiang; Sun, Rui; Ren, Jiaqi; Zhang, Cai’e; He, Feng; Woo, HanYoung; Min, Jie; Yang, Chuluo
Asymmetric side-chain substitution enables a 3D network acceptor with hydrogen bond assisted crystal packing and enhanced electronic coupling for efficient organic solar cells
Energy & Environmental Science, 2022, 15, 4601-4611
1567671 CIFC19 H17 N O3P 1 21/n 18.9115; 18.9555; 9.6086
90; 104.43; 90
1571.9Tavernier, Romain; Granado, Lérys; Tillard, Monique; Van Renterghem, Louis; Métro, Thomas-Xavier; Lamaty, Frédéric; Bonnaud, Leïla; Raquez, Jean-Marie; David, Ghislain; Caillol, Sylvain
Solvent-free synthesis of a formaldehyde-free benzoxazine monomer: study of its curing acceleration effect for commercial benzoxazine
Polymer Chemistry, 2022, 13, 5745-5756
1567672 CIFC37 H40 Cl N2 PdP 1 2/n 122.26; 14.479; 22.541
90; 106.1; 90
6980Zhou, Tongliang; Gao, Pengcheng; Bisz, Elwira; Dziuk, Błażej; Lalancette, Roger; Szostak, Roman; Szostak, Michal
Well-defined, air- and moisture-stable palladium–imidazo[1,5-a]pyridin-3-ylidene complexes: a versatile catalyst platform for cross-coupling reactions by L-shaped NHC ligands
Catalysis Science & Technology, 2022, 12, 6581-6589
1567673 CIFC31 H37 Cl N2 PdP b c a15.8974; 16.5103; 21.77
90; 90; 90
5714Zhou, Tongliang; Gao, Pengcheng; Bisz, Elwira; Dziuk, Błażej; Lalancette, Roger; Szostak, Roman; Szostak, Michal
Well-defined, air- and moisture-stable palladium–imidazo[1,5-a]pyridin-3-ylidene complexes: a versatile catalyst platform for cross-coupling reactions by L-shaped NHC ligands
Catalysis Science & Technology, 2022, 12, 6581-6589
1567674 CIFC41 H47 Cl N2 PdP b c a19.238; 17.9782; 21.2489
90; 90; 90
7349.2Zhou, Tongliang; Gao, Pengcheng; Bisz, Elwira; Dziuk, Błażej; Lalancette, Roger; Szostak, Roman; Szostak, Michal
Well-defined, air- and moisture-stable palladium–imidazo[1,5-a]pyridin-3-ylidene complexes: a versatile catalyst platform for cross-coupling reactions by L-shaped NHC ligands
Catalysis Science & Technology, 2022, 12, 6581-6589
1567675 CIFC40 H47 Cl N2 PdP b c a14.159; 17.0852; 29.6394
90; 90; 90
7170Zhou, Tongliang; Gao, Pengcheng; Bisz, Elwira; Dziuk, Błażej; Lalancette, Roger; Szostak, Roman; Szostak, Michal
Well-defined, air- and moisture-stable palladium–imidazo[1,5-a]pyridin-3-ylidene complexes: a versatile catalyst platform for cross-coupling reactions by L-shaped NHC ligands
Catalysis Science & Technology, 2022, 12, 6581-6589
1567676 CIFC39 H36 Ge N2P 1 21/c 115.0811; 11.4764; 18.5521
90; 90.197; 90
3210.9Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567677 CIFC39 H36 Ge N2 SP 1 21/n 17.9949; 21.1802; 19.6152
90; 99.409; 90
3276.8Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567678 CIFC39 H49 Ge N3 Si2P 1 21/n 113.302; 9.7758; 28.456
90; 93.909; 90
3691.7Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567679 CIFC78 H98 Cu2 Ge2 I2 N6 Se2 Si4P 1 21/c 113.7954; 12.2314; 23.9124
90; 90.032; 90
4034.9Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567680 CIFC39 H36 Ge N2 SeP 1 21/n 18.0415; 21.217; 19.7259
90; 99.617; 90
3318.3Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567681 CIFC39 H49 Ge N3 Se Si2P -18.9661; 11.2946; 19.9064
86.969; 77.252; 73.433
1884.5Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567682 CIFC42 H55 Ge N3 S Si2P -18.7695; 11.3819; 21.887
76.889; 86.438; 72.957
2034.2Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567683 CIFC39 H49 Cl Cu Ge N3 S Si2P -110.915; 12.0113; 17.7694
83.36; 76.387; 69.278
2116.37Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567684 CIFC35 H36 Ge N2 O SP 1 21/n 114.9611; 14.0451; 15.5244
90; 107.287; 90
3114.79Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567685 CIFC84 H112 Br2 Cu2 Ge2 N6 S2 Si4P -112.3707; 12.4183; 16.7015
89.009; 74.715; 61.241
2151.41Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567686 CIFC78 H98 Cu2 Ge2 I2 N6 S2 Si4P 1 21/c 113.947; 12.306; 23.936
90; 90.327; 90
4108.1Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567687 CIFC13 H8 Cu N2 O4 SP 1 21/n 16.17103; 31.0014; 6.95964
90; 93.726; 90
1328.64Xu, Heng; Zhang, Le-Xi; Xing, Yue; Yin, Yanyan; Tang, Bo; Bie, Lijian
Self-assembled mononuclear complexes: open metal sites and inverse dimension-dependent catalytic activity for Knoevenagel condensation and CO2 cycloaddition
Nanoscale, 2022
1567688 CIFC19 H18 Cu N2 O7 SP 1 21/n 14.9913; 26.3098; 14.5516
90; 95.274; 90
1902.83Xu, Heng; Zhang, Le-Xi; Xing, Yue; Yin, Yanyan; Tang, Bo; Bie, Lijian
Self-assembled mononuclear complexes: open metal sites and inverse dimension-dependent catalytic activity for Knoevenagel condensation and CO2 cycloaddition
Nanoscale, 2022
1567689 CIFC17 H18 N2 O7 S ZnP b c a16.0233; 14.6001; 16.6104
90; 90; 90
3885.87Xu, Heng; Zhang, Le-Xi; Xing, Yue; Yin, Yanyan; Tang, Bo; Bie, Lijian
Self-assembled mononuclear complexes: open metal sites and inverse dimension-dependent catalytic activity for Knoevenagel condensation and CO2 cycloaddition
Nanoscale, 2022
1567690 CIFC17 H18 Cu N2 O7 SP b c a16.10966; 14.61582; 16.4897
90; 90; 90
3882.6Xu, Heng; Zhang, Le-Xi; Xing, Yue; Yin, Yanyan; Tang, Bo; Bie, Lijian
Self-assembled mononuclear complexes: open metal sites and inverse dimension-dependent catalytic activity for Knoevenagel condensation and CO2 cycloaddition
Nanoscale, 2022
1567691 CIF
Paper
C20 H16 N2 O6P 1 21/c 119.0804; 4.6758; 10.1189
90; 101.169; 90
885.67Martínez-de la Luz, Isabel; López-Velázquez, Delia; Bernès, Sylvain; Varela Caselis, Jenaro L.
Bis(4-hydroxyphenyl) 1,4-phenylenebiscarbamate
IUCrData, 2022, 7, x220919
1567692 CIF
Paper
C18 H16 N2 O2P 1 21/c 18.2745; 7.9167; 23.0663
90; 93.225; 90
1508.61Archana, Sreeramapura D.; Nagma Banu, Holalagudu A.; Kalluraya, Balakrishna; Yathirajan, Hemmige S.; Balerao, Rishik; Butcher, Ray J.
3-Methyl-5-(4-methylphenoxy)-1-phenyl-1<i>H</i>-pyrazole-4-carbaldehyde
IUCrData, 2022, 7, x220924
1567693 CIF
Paper
C20 H12 N2 O2 SP -18.1891; 8.2417; 12.813
81.632; 81.394; 66.649
781.5Okuno, Tsunehisa; Doi, Ikue
10-[(4-Nitrophenyl)ethynyl]-10<i>H</i>-phenothiazine
IUCrData, 2022, 7, x220942
1567694 CIF
Paper
C21 H18 O4C 1 2/c 115.8594; 5.0437; 40.6908
90; 90.507; 90
3254.7Koh, Dongsoo
(<i>E</i>)-1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-(naphthalen-1-yl)prop-2-en-1-one
IUCrData, 2022, 7, x220932
1567695 CIFC32 H30 O2P 1 21 19.5099; 9.8152; 13.7004
90; 105.846; 90
1230.22Arkhypchuk, Anna I.; D'Imperio, Nicolas; Wells, Jordann A. L.; Ott, Sascha
[2 + 2] Cycloaddition of phosphaalkenes as a key step for the reductive coupling of diaryl ketones to tetraaryl olefins
Chemical Science, 2022, 13, 12239-12244
1567696 CIFC34 H26 O2P 1 21 19.2899; 10.6993; 13.1402
90; 107.074; 90
1248.51Arkhypchuk, Anna I.; D'Imperio, Nicolas; Wells, Jordann A. L.; Ott, Sascha
[2 + 2] Cycloaddition of phosphaalkenes as a key step for the reductive coupling of diaryl ketones to tetraaryl olefins
Chemical Science, 2022, 13, 12239-12244
1567697 CIFC36 H36 F2 O2P 1 21/c 110.356; 31.286; 9.517
90; 108.01; 90
2932.4Arkhypchuk, Anna I.; D'Imperio, Nicolas; Wells, Jordann A. L.; Ott, Sascha
[2 + 2] Cycloaddition of phosphaalkenes as a key step for the reductive coupling of diaryl ketones to tetraaryl olefins
Chemical Science, 2022, 13, 12239-12244
1567698 CIFC33 H29 Cl3 F2 O2P 1 21/n 113.893; 9.559; 23.43
90; 98.908; 90
3074Arkhypchuk, Anna I.; D'Imperio, Nicolas; Wells, Jordann A. L.; Ott, Sascha
[2 + 2] Cycloaddition of phosphaalkenes as a key step for the reductive coupling of diaryl ketones to tetraaryl olefins
Chemical Science, 2022, 13, 12239-12244
1567699 CIFC48 H57 P3 Si3C 1 2/c 126.6644; 42.3661; 9.7021
90; 104.927; 90
10590.3Arkhypchuk, Anna I.; D'Imperio, Nicolas; Wells, Jordann A. L.; Ott, Sascha
[2 + 2] Cycloaddition of phosphaalkenes as a key step for the reductive coupling of diaryl ketones to tetraaryl olefins
Chemical Science, 2022, 13, 12239-12244
1567700 CIFC16 H18 O4 SP 1 21/n 19.1786; 18.5224; 9.2041
90; 107.616; 90
1491.41Zhang, Chun; Yang, Man; Qiu, Yanjie; Song, Meijun; Wang, Hongyan; Yang, Min; Xie, Wenlin; Wu, Jie; Ye, Shengqing
Alkoxysulfonyl Radical Species: Acquisition and Transformation towards Sulfonate Esters through Electrochemistry
Chemical Science, 2022
1567701 CIFC14 H20 O4 SP 1 21/c 111.5469; 8.3647; 15.835
90; 105.211; 90
1475.9Zhang, Chun; Yang, Man; Qiu, Yanjie; Song, Meijun; Wang, Hongyan; Yang, Min; Xie, Wenlin; Wu, Jie; Ye, Shengqing
Alkoxysulfonyl Radical Species: Acquisition and Transformation towards Sulfonate Esters through Electrochemistry
Chemical Science, 2022
1567702 CIFC24 H23 N O3P 21 21 217.9494; 10.2838; 24.4594
90; 90; 90
1999.56Li, Wendeng; Zhang, He; Chen, Kai; Jiang, Huanfeng; Sun, Jianwei; Zhu, Shifa
Palladium-catalyzed intramolecular enantioselective C(sp3)–H insertion of donor/donor carbenes
Chemical Science, 2022, 13, 12396-12402
1567703 CIFC28 H25 N O2 SP 3110.2503; 10.2503; 18.6428
90; 90; 120
1696.35Li, Wendeng; Zhang, He; Chen, Kai; Jiang, Huanfeng; Sun, Jianwei; Zhu, Shifa
Palladium-catalyzed intramolecular enantioselective C(sp3)–H insertion of donor/donor carbenes
Chemical Science, 2022, 13, 12396-12402
1567704 CIFC27 H23 N O2 SP 1 21 19.4589; 9.3504; 12.948
90; 110.298; 90
1074.06Li, Wendeng; Zhang, He; Chen, Kai; Jiang, Huanfeng; Sun, Jianwei; Zhu, Shifa
Palladium-catalyzed intramolecular enantioselective C(sp3)–H insertion of donor/donor carbenes
Chemical Science, 2022, 13, 12396-12402
1567705 CIFC17 H18 O2P 21 21 216.444; 8.3645; 24.703
90; 90; 90
1331.5Stegbauer, Simone; Jandl, Christian; Bach, Thorsten
Chiral Lewis acid catalysis in a visible light-triggered cycloaddition/rearrangement cascade
Chemical Science, 2022
1567706 CIFC17 H17 Cl O2P 1 21 16.0803; 8.5188; 13.8407
90; 90.32; 90
716.89Stegbauer, Simone; Jandl, Christian; Bach, Thorsten
Chiral Lewis acid catalysis in a visible light-triggered cycloaddition/rearrangement cascade
Chemical Science, 2022
1567707 CIFC19 H20 O2 SP 21 21 216.4656; 13.7036; 17.0877
90; 90; 90
1514Stegbauer, Simone; Jandl, Christian; Bach, Thorsten
Chiral Lewis acid catalysis in a visible light-triggered cycloaddition/rearrangement cascade
Chemical Science, 2022
1567708 CIFC16 H14 N2 O2P 1 21/c 126.505; 5.5966; 9.4104
90; 98.519; 90
1380.5Dasgupta, Ayan; Guerzoni, Michael G.; Alotaibi, Nusaybah; van Ingen, Yara; Farshadfar, Kaveh; Richards, Emma; Ariafard, Alireza; Melen, Rebecca L.
Chemo- and regio-selective amidation of indoles with isocyanates using borane Lewis acids
Catalysis Science & Technology, 2022, 12, 5982-5990
1567709 CIFC15 H12 N2 OP 1 21/c 15.5956; 23.7388; 9.2195
90; 99.725; 90
1207.05Dasgupta, Ayan; Guerzoni, Michael G.; Alotaibi, Nusaybah; van Ingen, Yara; Farshadfar, Kaveh; Richards, Emma; Ariafard, Alireza; Melen, Rebecca L.
Chemo- and regio-selective amidation of indoles with isocyanates using borane Lewis acids
Catalysis Science & Technology, 2022, 12, 5982-5990
1567710 CIFC34 H13 B Cl F15 N2 OP -18.0666; 12.7868; 15.6641
77.581; 87.401; 78.419
1545.76Dasgupta, Ayan; Guerzoni, Michael G.; Alotaibi, Nusaybah; van Ingen, Yara; Farshadfar, Kaveh; Richards, Emma; Ariafard, Alireza; Melen, Rebecca L.
Chemo- and regio-selective amidation of indoles with isocyanates using borane Lewis acids
Catalysis Science & Technology, 2022, 12, 5982-5990
1567711 CIFC34 H14 B F15 N2 OP -17.9694; 12.4723; 15.5816
78.311; 86.618; 79.065
1488.76Dasgupta, Ayan; Guerzoni, Michael G.; Alotaibi, Nusaybah; van Ingen, Yara; Farshadfar, Kaveh; Richards, Emma; Ariafard, Alireza; Melen, Rebecca L.
Chemo- and regio-selective amidation of indoles with isocyanates using borane Lewis acids
Catalysis Science & Technology, 2022, 12, 5982-5990
1567712 CIFC8 H7 B Cl3 NC 1 2/m 115.121; 6.9264; 9.8879
90; 109.906; 90
973.7Dasgupta, Ayan; Guerzoni, Michael G.; Alotaibi, Nusaybah; van Ingen, Yara; Farshadfar, Kaveh; Richards, Emma; Ariafard, Alireza; Melen, Rebecca L.
Chemo- and regio-selective amidation of indoles with isocyanates using borane Lewis acids
Catalysis Science & Technology, 2022, 12, 5982-5990
1567713 CIFC36 H17 B Br Cl4 F10 N3 O2P -112.7275; 16.2624; 19.5564
69.141; 77.001; 87.734
3681.9Dasgupta, Ayan; Guerzoni, Michael G.; Alotaibi, Nusaybah; van Ingen, Yara; Farshadfar, Kaveh; Richards, Emma; Ariafard, Alireza; Melen, Rebecca L.
Chemo- and regio-selective amidation of indoles with isocyanates using borane Lewis acids
Catalysis Science & Technology, 2022, 12, 5982-5990
1567714 CIFC25 H25 Cl N2 O SiP -110.0506; 12.4111; 19.1784
99.504; 93.559; 90.568
2354.4Dasgupta, Ayan; Guerzoni, Michael G.; Alotaibi, Nusaybah; van Ingen, Yara; Farshadfar, Kaveh; Richards, Emma; Ariafard, Alireza; Melen, Rebecca L.
Chemo- and regio-selective amidation of indoles with isocyanates using borane Lewis acids
Catalysis Science & Technology, 2022, 12, 5982-5990
1567715 CIFC13 H26 N2 OC 1 2/c 116.5207; 9.9632; 34.818
90; 91.771; 90
5728.3Dasgupta, Ayan; Guerzoni, Michael G.; Alotaibi, Nusaybah; van Ingen, Yara; Farshadfar, Kaveh; Richards, Emma; Ariafard, Alireza; Melen, Rebecca L.
Chemo- and regio-selective amidation of indoles with isocyanates using borane Lewis acids
Catalysis Science & Technology, 2022, 12, 5982-5990
1567716 CIFC16 H14 N2 OP 1 21/c 122.5646; 13.0075; 8.9569
90; 95.53; 90
2616.7Dasgupta, Ayan; Guerzoni, Michael G.; Alotaibi, Nusaybah; van Ingen, Yara; Farshadfar, Kaveh; Richards, Emma; Ariafard, Alireza; Melen, Rebecca L.
Chemo- and regio-selective amidation of indoles with isocyanates using borane Lewis acids
Catalysis Science & Technology, 2022, 12, 5982-5990
1567717 CIFC13 H5 Cl F5 N OP 1 21/n 15.6086; 9.3087; 23.8205
90; 90.95; 90
1243.47Dasgupta, Ayan; Guerzoni, Michael G.; Alotaibi, Nusaybah; van Ingen, Yara; Farshadfar, Kaveh; Richards, Emma; Ariafard, Alireza; Melen, Rebecca L.
Chemo- and regio-selective amidation of indoles with isocyanates using borane Lewis acids
Catalysis Science & Technology, 2022, 12, 5982-5990
1567718 CIFC23 H18 Cl N3 O2P 21 21 215.7822; 12.3852; 27.1093
90; 90; 90
1941.4Dasgupta, Ayan; Guerzoni, Michael G.; Alotaibi, Nusaybah; van Ingen, Yara; Farshadfar, Kaveh; Richards, Emma; Ariafard, Alireza; Melen, Rebecca L.
Chemo- and regio-selective amidation of indoles with isocyanates using borane Lewis acids
Catalysis Science & Technology, 2022, 12, 5982-5990
1567719 CIFC14 H11 N O SP 1 21/c 19.6609; 6.3361; 19.6298
90; 96.172; 90
1194.62Dhara, Samiran; Saha, Moumita; Das, Asish R.
Ligand-free access to benzisothiazolones and benzisoselenazolones through NiFe <sub>2</sub> O <sub>4</sub> catalyzed concomitant annulation of 2-halobenzanilides with chalcogens and their late-stage transformations
New Journal of Chemistry, 2022, 46, 19501-19513
1567720 CIF
Paper
C18 H13 N O4P -17.6534; 8.6079; 11.369
94.433; 97.953; 97.019
732.8Vinaya; Basavaraju, Yeriyur B.; Nagma Banu, Holalagudu A.; Kalluraya, Balakrishna; Yathirajan, Hemmige S.; Balerao, Rishik; Butcher, Ray J.
3-(3-Nitrophenyl)-1-[4-(prop-2-ynyloxy)phenyl]prop-2-en-1-one
IUCrData, 2022, 7, x220957
1567721 CIFC148 H108 Au8 O10 P6 S2P 21 21 2118.8119; 27.697; 31.3398
90; 90; 90
16329.1Si, Wei-Dan; Sheng, Kai; Zhang, Chengkai; Wang, Zhi; Zhang, Shan-Shan; Dou, Jian-Min; Feng, Lei; Gao, Zhi-Yong; Tung, Chen-Ho; Sun, Di
Bicarbonate insertion triggered self-assembly of chiral octa-gold nanoclusters into helical superstructures in the crystalline state
Chemical Science, 2022, 13, 10523-10531
1567722 CIFC146 H104 Au8 O4 P6 S2P 21 21 2120.5564; 25.7288; 26.0976
90; 90; 90
13802.8Si, Wei-Dan; Sheng, Kai; Zhang, Chengkai; Wang, Zhi; Zhang, Shan-Shan; Dou, Jian-Min; Feng, Lei; Gao, Zhi-Yong; Tung, Chen-Ho; Sun, Di
Bicarbonate insertion triggered self-assembly of chiral octa-gold nanoclusters into helical superstructures in the crystalline state
Chemical Science, 2022, 13, 10523-10531
1567723 CIFC148 H108 Au8 O10 P6 S2P 21 21 2118.4744; 27.7085; 31.2344
90; 90; 90
15988.8Si, Wei-Dan; Sheng, Kai; Zhang, Chengkai; Wang, Zhi; Zhang, Shan-Shan; Dou, Jian-Min; Feng, Lei; Gao, Zhi-Yong; Tung, Chen-Ho; Sun, Di
Bicarbonate insertion triggered self-assembly of chiral octa-gold nanoclusters into helical superstructures in the crystalline state
Chemical Science, 2022, 13, 10523-10531
1567724 CIFC146 H104 Au8 O4 P6 S2P 21 21 2120.333; 25.812; 26.048
90; 90; 90
13671Si, Wei-Dan; Sheng, Kai; Zhang, Chengkai; Wang, Zhi; Zhang, Shan-Shan; Dou, Jian-Min; Feng, Lei; Gao, Zhi-Yong; Tung, Chen-Ho; Sun, Di
Bicarbonate insertion triggered self-assembly of chiral octa-gold nanoclusters into helical superstructures in the crystalline state
Chemical Science, 2022, 13, 10523-10531
1567725 CIFC26 H26 F N2 OP 1 21/c 111.1117; 20.386; 9.6205
90; 107.152; 90
2082.34Rai, Pramod; Maji, Kakoli; Jana, Sayan K.; Maji, Biplab
Intermolecular dearomative [4 + 2] cycloaddition of naphthalenes via visible-light energy-transfer-catalysis
Chemical Science, 2022, 13, 12503-12510
1567726 CIFC20 H17 F OF d d 238.8063; 15.6732; 9.8717
90; 90; 90
6004.15Rai, Pramod; Maji, Kakoli; Jana, Sayan K.; Maji, Biplab
Intermolecular dearomative [4 + 2] cycloaddition of naphthalenes via visible-light energy-transfer-catalysis
Chemical Science, 2022, 13, 12503-12510
1567727 CIFC23 H19 F N2 OP 1 21/c 112.6548; 7.2987; 20.6049
90; 98.643; 90
1881.53Rai, Pramod; Maji, Kakoli; Jana, Sayan K.; Maji, Biplab
Intermolecular dearomative [4 + 2] cycloaddition of naphthalenes via visible-light energy-transfer-catalysis
Chemical Science, 2022, 13, 12503-12510
1567728 CIFC20 H17 Cl OP 1 21/c 19.4028; 19.5701; 9.3681
90; 115.798; 90
1552.05Rai, Pramod; Maji, Kakoli; Jana, Sayan K.; Maji, Biplab
Intermolecular dearomative [4 + 2] cycloaddition of naphthalenes via visible-light energy-transfer-catalysis
Chemical Science, 2022, 13, 12503-12510
1567729 CIFC22 H19 F O3P 1 21/c 113.8641; 10.5226; 12.1171
90; 103.029; 90
1722.21Rai, Pramod; Maji, Kakoli; Jana, Sayan K.; Maji, Biplab
Intermolecular dearomative [4 + 2] cycloaddition of naphthalenes via visible-light energy-transfer-catalysis
Chemical Science, 2022, 13, 12503-12510
1567730 CIFC27 H57 N O6 SP 1 21/c 130.686; 7.524; 41.837
90; 97.104; 90
9585.2Ravindar, Chinapaka; Reddy, S. Thirupathi; Sivaramakrishna, Dokku; Damera, Deepthi Priyanka; Swamy, Musti J.
Base-triggerable lauryl sarcosinate-dodecyl sulfate catanionic liposomes: structure, biophysical characterization, and drug entrapment/release studies.
Soft matter, 2022, 18, 7814-7826
1567731 CIFC904 H1758 Cl24 N48 O230 Pd12 S200C m m a54.9549; 61.3516; 56.7355
90; 90; 90
191288Li, Ru-Jin; Tarzia, Andrew; Posligua, Victor; Jelfs, Kim E.; Sanchez, Nicolas; Marcus, Adam; Baksi, Ananya; Clever, Guido H.; Fadaei-Tirani, Farzaneh; Severin, Kay
Orientational self-sorting in cuboctahedral Pd cages
Chemical Science, 2022
1567732 CIFC27 H28 N2 O4 S2P 1 21/n 19.4288; 10.4362; 26.2815
90; 96.065; 90
2571.65Chen, Zhi; Li, Yu-Fan; Tan, Shun-Zhong; Ouyang, Qin; Chen, Zhi-Chao; Du, Wei; Chen, Ying-Chun
Formal nucleophilic pyrrolylmethylation via palladium-based auto-tandem catalysis: switchable regiodivergent synthesis and remote chirality transfer
Chemical Science, 2022, 13, 12433-12439
1567733 CIFC31 H30 N2 O4 S3C 1 2/c 129.5374; 9.77; 24.882
90; 122.932; 90
6026.7Chen, Zhi; Li, Yu-Fan; Tan, Shun-Zhong; Ouyang, Qin; Chen, Zhi-Chao; Du, Wei; Chen, Ying-Chun
Formal nucleophilic pyrrolylmethylation via palladium-based auto-tandem catalysis: switchable regiodivergent synthesis and remote chirality transfer
Chemical Science, 2022, 13, 12433-12439
1567734 CIFC26 H39 F6 N O4 SiP -17.2552; 13.8552; 15.7314
105.333; 99.3403; 101.607
1454.49Sungnoi, Wanna; Harmata, Michael
Oxidative bridgehead functionalization of (4 + 3) cycloadducts obtained from oxidopyridinium ions
RSC Advances, 2022, 12, 28572-28575
1567735 CIFC2 H5 N O2P 316.9848; 6.9848; 5.4744
90; 90; 120
231.3Balashova, Elena; Levin, Aleksandr A.; Davydov, Valery; Smirnov, Alexander; Starukhin, Anatoly; Pavlov, Sergey; Krichevtsov, Boris; Zolotarev, Andrey; Zhang, Hongjun; Li, Fangzhe; Ke, Hua
Croconic Acid Doped Glycine Single Crystals: Growth, Crystal Structure, UV-Vis, FTIR, Raman and Photoluminescence Spectroscopy
Crystals, 2022, 12, 1342
1567736 CIFC2 H5 N O2P 1 21/n 15.1004; 11.9664; 5.457
90; 111.714; 90
309.43Balashova, Elena; Levin, Aleksandr A.; Davydov, Valery; Smirnov, Alexander; Starukhin, Anatoly; Pavlov, Sergey; Krichevtsov, Boris; Zolotarev, Andrey; Zhang, Hongjun; Li, Fangzhe; Ke, Hua
Croconic Acid Doped Glycine Single Crystals: Growth, Crystal Structure, UV-Vis, FTIR, Raman and Photoluminescence Spectroscopy
Crystals, 2022, 12, 1342
1567737 CIFC24 H24 In N3 S6P -114.6017; 14.9653; 15.3953
62.209; 76.315; 72.31
2817.4Ferjani, Hela; Onwudiwe, Damian C.
Synthesis, Structural, Thermal, and Hirshfeld Surface Analysis of In(III) Tris (N-Methyl-N-Phenyl Dithiocarbamate)
Inorganics, 2022, 10, 146
1567738 CIFC44 H45 B8 Cl O P2 Ru2P -110.56; 20.205; 22.352
114.814; 101.57; 90.753
4215.4Loginov, Dmitry A.; Dolgushin, Fedor M.; Konoplev, Vitalii E.; Tachaev, Maxim V.
New Aspects of Ruthenium-Mediated Polyhedral Contraction of Monocarbollides
Inorganics, 2022, 10, 158
1567739 CIFC46 H49 B8 Cl5 O P2 RuP 1 21/c 118.467; 15.515; 18.611
90; 100.17; 90
5249Loginov, Dmitry A.; Dolgushin, Fedor M.; Konoplev, Vitalii E.; Tachaev, Maxim V.
New Aspects of Ruthenium-Mediated Polyhedral Contraction of Monocarbollides
Inorganics, 2022, 10, 158
1567740 CIFC92 H90 Al8 F72 Ga2 O8P 1 21/c 144.352; 18.147; 30.839
90; 102.49; 90
24234Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567741 CIFC55 H66 Al4 F36 Ga N3 O4P -117.181; 21.399; 21.691
117.464; 90.245; 90.863
7075Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567742 CIFC56.88 H67.67 Al4 F36.06 Ga N3 O3.97P -110.927; 17.637; 19.087
94.601; 97.945; 98.66
3582Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567743 CIFC55 H66 Al5 F36 N3 O4P 1 21/c 121.369; 17.024; 21.581
90; 116.118; 90
7049Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567744 CIFC52.45 H49.31 Al4 F38.14 Ga O4P -116.445; 16.685; 28.346
80.473; 83.826; 60.715
6687Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567745 CIFC48.13 H46.42 Al4 F36.71 O4 TlP -122.345; 26.95; 29.77
88.88; 70.81; 70.94
15925Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567746 CIFC48.1 H46.39 Al4 F36.73 In O4P -122.327; 26.903; 29.692
88.983; 70.929; 70.884
15847Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567747 CIFC40 Ca21 O278 U24P -4 n 224.6098; 24.6098; 24.6246
90; 90; 90
14913.7Tyumentseva, Olga S.; Kornyakov, Ilya V.; Kasatkin, Anatoly V.; Plášil, Jakub; Krzhizhanovskaya, Maria G.; Krivovichev, Sergey V.; Burns, Peter C.; Gurzhiy, Vladislav V.
One of Nature’s Puzzles Is Assembled: Analog of the Earth’s Most Complex Mineral, Ewingite, Synthesized in a Laboratory
Materials, 2022, 15, 6643
1567748 CIFC3 H6 N2 OF d d d :29.97; 11.8236; 13.3559
90; 90; 90
1574.41Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567749 CIFC3 H10 F6 N3 O PP -15.25069; 7.8976; 11.4023
82.781; 79.266; 84.108
459.35Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567750 CIFC2 H12 N8 O6P 1 21/n 114.6572; 3.71857; 20.3958
90; 108.778; 90
1052.48Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567751 CIFC3 H10 N6 O5C 1 2/c 124.756; 4.29; 17.8827
90; 107.988; 90
1806.37Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567752 CIFC2 H12 N8 O6P 1 21/n 114.7309; 3.59237; 20.2453
90; 108.791; 90
1014.25Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567753 CIFC2 H6 F6 N2 O PP 1 21/c 111.4292; 5.5925; 11.1451
90; 92.547; 90
711.67Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567754 CIFC H8 F6 N3 O PP b c a7.67243; 8.07957; 24.2351
90; 90; 90
1502.33Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567755 CIFC312 H362 Ag30 B3 Cl5 N4 P8 Pt S14P -121.6373; 23.8035; 34.2827
96.657; 100.949; 100.389
16844Wang, Silan; Li, Qinzhen; Yang, Sha; Yu, Haizhu; Chai, Jinsong; Zhu, Manzhou
H-bond-induced luminescence enhancement in Pt1Ag30 nanocluster and its application in methanol detection
Nanoscale, 2022
1567756 CIFC66.95 H108.34 N0.52 O21.95 V6P b c m14.4807; 27.8595; 18.7836
90; 90; 90
7577.77Cooney, Shannon E.; Fertig, Alex A.; Buisch, Madeleine R.; Brennessel, William W.; Matson, Ellen M.
Coordination-induced bond weakening of water at the surface of an oxygen-deficient polyoxovanadate cluster.
Chemical science, 2022, 13, 12726-12737
1567757 CIFC21 H23 F O4P 1 21 18.092; 5.9484; 19.5057
90; 98.051; 90
929.64Liao, Ling; Zhang, Ying; Wu, Zhong-Wei; Ye, Zhong-Tian; Zhang, Xue-Xin; Chen, Guangying; Yu, Jin-Sheng
Nickel-catalyzed regio- and enantio-selective Markovnikov hydromonofluoroalkylation of 1,3-dienes
Chemical Science, 2022, 13, 12519-12526
1567758 CIFC23 H21 F O4 S2P 21 21 217.5543; 10.058; 28.1125
90; 90; 90
2136.02Liao, Ling; Zhang, Ying; Wu, Zhong-Wei; Ye, Zhong-Tian; Zhang, Xue-Xin; Chen, Guangying; Yu, Jin-Sheng
Nickel-catalyzed regio- and enantio-selective Markovnikov hydromonofluoroalkylation of 1,3-dienes
Chemical Science, 2022, 13, 12519-12526
1567759 CIFC13 H20.2 N2 O2.1P -15.7302; 9.9783; 11.5048
83.662; 89.167; 86.054
652.23Tien, Chieh-Hung; Lough, Alan J.; Yudin, Andrei K.
Iminologous epoxide ring-closure
Chemical Science, 2022, 13, 12175-12179
1567760 CIFC13 H19 N O5P 1 21/c 111.2115; 11.5329; 11.145
90; 104.981; 90
1392.08Tien, Chieh-Hung; Lough, Alan J.; Yudin, Andrei K.
Iminologous epoxide ring-closure
Chemical Science, 2022, 13, 12175-12179
1567761 CIFC13 H20 B F3 N2 O3C 1 2/c 131.0762; 9.4685; 12.1756
90; 91.156; 90
3581.9Tien, Chieh-Hung; Lough, Alan J.; Yudin, Andrei K.
Iminologous epoxide ring-closure
Chemical Science, 2022, 13, 12175-12179
1567762 CIFC22 H34 N2 O5 SP b c a16.617; 11.8972; 22.9385
90; 90; 90
4534.8Tien, Chieh-Hung; Lough, Alan J.; Yudin, Andrei K.
Iminologous epoxide ring-closure
Chemical Science, 2022, 13, 12175-12179
1567763 CIFC12 H10 Br F N2 SP 14.5926; 5.6626; 12.165
86.311; 88.909; 81.003
311.81Zhao, Ruyan; Zhu, Tong; Wang, Sasa; Jarrett-Wilkins, Charlie; Najjarian, Amin Morteza; Lough, Alan J.; Hoogland, Sjoerd; Sargent, Edward H.; Seferos, Dwight S.
Engineering hydrogen bonding to align molecular dipoles in organic solids for efficient second harmonic generation
Chemical Science, 2022, 13, 12144-12148
1567764 CIFC12 H11 Br2 F N2 SP -14.5711; 12.769; 13.073
69.971; 89.227; 85.826
714.9Zhao, Ruyan; Zhu, Tong; Wang, Sasa; Jarrett-Wilkins, Charlie; Najjarian, Amin Morteza; Lough, Alan J.; Hoogland, Sjoerd; Sargent, Edward H.; Seferos, Dwight S.
Engineering hydrogen bonding to align molecular dipoles in organic solids for efficient second harmonic generation
Chemical Science, 2022, 13, 12144-12148
1567765 CIF
Paper
C49 H46 B N5P -113.5215; 13.5537; 13.6079
92.202; 113.379; 117.604
1951.3Shimazaki, Runa; Sadakiyo, Masaaki
Ethidium tetraphenylborate acetonitrile disolvate
IUCrData, 2022, 7, x220951
1567766 CIF
Paper
C35 H57.5 N O3.25P 111.8289; 16.7287; 17.7234
116.207; 91.0059; 100.454
3075.4Campos Fernandez, Cristian; Procupez-Schtirbu, R.; Soto-Tellini, V. H.; Salazar, J. C.; Jancik, Vojtech
(1<i>S</i>,3<i>R</i>)-<i>N</i>-{(3<i>S</i>,10<i>S</i>,12<i>S</i>,13<i>R</i>,17<i>R</i>)-12-Hydroxy-17-[(<i>R</i>)-5-hydroxypentan-2-yl]-10,13-dimethylhexadecahydro-1<i>H</i>-cyclopenta[<i>a</i>]phenanthren-3-yl}adamantane-1-carboxamide 0.25-hydrate
IUCrData, 2022, 7, x220947
1567767 CIFC58 H82 Cl2 Ga2 N4 P2P 1 21/n 113.701; 13.8715; 15.7041
90; 105.336; 90
2878.3Sharma, Mahendra K.; Chabbra, Sonia; Wölper, Christoph; Weinert, Hanns Micha; Reijerse, Edward; Schnegg, Alexander; Schulz, Stephan
Modulating the Frontier Orbitals of L(X)Ga-Substituted Diphosphenes [L(X)GaP]2 (X = Cl, Br) and their Facile Oxidation to Radical Cations
Chemical Science, 2022
1567768 CIFC96 H102 B Cl2 F20 Ga2 N6 P2P -112.6151; 16.6393; 23.1348
77.844; 77.731; 86.897
4638.6Sharma, Mahendra K.; Chabbra, Sonia; Wölper, Christoph; Weinert, Hanns Micha; Reijerse, Edward; Schnegg, Alexander; Schulz, Stephan
Modulating the Frontier Orbitals of L(X)Ga-Substituted Diphosphenes [L(X)GaP]2 (X = Cl, Br) and their Facile Oxidation to Radical Cations
Chemical Science, 2022
1567769 CIFC89 H95 B Cl2 F20 Ga2 N6 P2P -112.5203; 16.6728; 23.1865
78.0634; 77.1747; 87.3124
4617.3Sharma, Mahendra K.; Chabbra, Sonia; Wölper, Christoph; Weinert, Hanns Micha; Reijerse, Edward; Schnegg, Alexander; Schulz, Stephan
Modulating the Frontier Orbitals of L(X)Ga-Substituted Diphosphenes [L(X)GaP]2 (X = Cl, Br) and their Facile Oxidation to Radical Cations
Chemical Science, 2022
1567770 CIFC68 H101 Br2 Ga2 N6 P2P 1 21/n 114.7131; 25.5509; 18.5397
90; 99.6843; 90
6870.4Sharma, Mahendra K.; Chabbra, Sonia; Wölper, Christoph; Weinert, Hanns Micha; Reijerse, Edward; Schnegg, Alexander; Schulz, Stephan
Modulating the Frontier Orbitals of L(X)Ga-Substituted Diphosphenes [L(X)GaP]2 (X = Cl, Br) and their Facile Oxidation to Radical Cations
Chemical Science, 2022
1567771 CIFC58 H82 Br2 Ga2 N4 P2P 1 21/n 113.6417; 13.9614; 15.7579
90; 105.102; 90
2897.6Sharma, Mahendra K.; Chabbra, Sonia; Wölper, Christoph; Weinert, Hanns Micha; Reijerse, Edward; Schnegg, Alexander; Schulz, Stephan
Modulating the Frontier Orbitals of L(X)Ga-Substituted Diphosphenes [L(X)GaP]2 (X = Cl, Br) and their Facile Oxidation to Radical Cations
Chemical Science, 2022
1567772 CIFC65 H94 Cl2 Ga2 N6 P2P -114.863; 20.33; 25.712
83.603; 75.258; 72.565
7163Sharma, Mahendra K.; Chabbra, Sonia; Wölper, Christoph; Weinert, Hanns Micha; Reijerse, Edward; Schnegg, Alexander; Schulz, Stephan
Modulating the Frontier Orbitals of L(X)Ga-Substituted Diphosphenes [L(X)GaP]2 (X = Cl, Br) and their Facile Oxidation to Radical Cations
Chemical Science, 2022
1567773 CIFC89 H95 B Br2 F20 Ga2 N6 P2P -112.5498; 16.689; 23.2672
77.921; 77.403; 87.595
4650.5Sharma, Mahendra K.; Chabbra, Sonia; Wölper, Christoph; Weinert, Hanns Micha; Reijerse, Edward; Schnegg, Alexander; Schulz, Stephan
Modulating the Frontier Orbitals of L(X)Ga-Substituted Diphosphenes [L(X)GaP]2 (X = Cl, Br) and their Facile Oxidation to Radical Cations
Chemical Science, 2022
1567774 CIFC89 H94 B Br2 F20 Ga2 N6 P2P 1 21/c 121.557; 20.432; 20.684
90; 99.72; 90
8979.5Sharma, Mahendra K.; Chabbra, Sonia; Wölper, Christoph; Weinert, Hanns Micha; Reijerse, Edward; Schnegg, Alexander; Schulz, Stephan
Modulating the Frontier Orbitals of L(X)Ga-Substituted Diphosphenes [L(X)GaP]2 (X = Cl, Br) and their Facile Oxidation to Radical Cations
Chemical Science, 2022
1567775 CIFC15 H14 O3P 21 21 217.7082; 12.0888; 12.3892
90; 90; 90
1154.46Guan, Fujun; Zhou, Rong; Ren, Xiaoyu; Guo, Zhen; Wang, Chengming; Zhou, Cong-Ying
Asymmetric dearomative cyclopropanation of naphthalenes to construct polycyclic compounds.
Chemical science, 2022, 13, 13015-13019
1567776 CIFC15 H13 Br O2P 21 21 217.0572; 10.6743; 15.6753
90; 90; 90
1180.83Guan, Fujun; Zhou, Rong; Ren, Xiaoyu; Guo, Zhen; Wang, Chengming; Zhou, Cong-Ying
Asymmetric dearomative cyclopropanation of naphthalenes to construct polycyclic compounds.
Chemical science, 2022, 13, 13015-13019
1567777 CIFC24 H27 Cl2 N2 P ZnP -19.6677; 11.6496; 12.2679
109.146; 112.87; 91.797
1182.45Cao, Furong; Wang, Yun; Wang, Xing; Zhang, Wenjuan; Solan, Gregory A.; Wang, Rui; Ma, Yanping; Hao, Xiang; Sun, Wen-Hua
Zinc 8-aminotrihydroquinolines appended with pendant N-diphenylphosphinoethyl arms as exceptionally active catalysts for the ROP of ε-CL
Catalysis Science & Technology, 2022, 12, 6687-6703
1567778 CIFC29 H29 Cl2 N2 P ZnP 1 21/n 114.5983; 11.3593; 16.4355
90; 101.497; 90
2670.76Cao, Furong; Wang, Yun; Wang, Xing; Zhang, Wenjuan; Solan, Gregory A.; Wang, Rui; Ma, Yanping; Hao, Xiang; Sun, Wen-Hua
Zinc 8-aminotrihydroquinolines appended with pendant N-diphenylphosphinoethyl arms as exceptionally active catalysts for the ROP of ε-CL
Catalysis Science & Technology, 2022, 12, 6687-6703
1567779 CIFC11 H14 Cl Fe O2 PP b c a12.2903; 13.3012; 15.6001
90; 90; 90
2550.24Xin, Tiansi; Geeson, Michael B.; Zhu, Hui; Qu, Zheng-Wang; Grimme, Stefan; Cummins, Christopher C.
Synthesis of phosphiranes <i>via</i> organoiron-catalyzed phosphinidene transfer to electron-deficient olefins.
Chemical science, 2022, 13, 12696-12702
1567780 CIFC15 H20 Cl Fe O4 PP 1 21/c 18.0716; 22.6406; 9.6109
90; 107.934; 90
1671.01Xin, Tiansi; Geeson, Michael B.; Zhu, Hui; Qu, Zheng-Wang; Grimme, Stefan; Cummins, Christopher C.
Synthesis of phosphiranes <i>via</i> organoiron-catalyzed phosphinidene transfer to electron-deficient olefins.
Chemical science, 2022, 13, 12696-12702

Blue left arrow Blue left arrow First | Blue left arrow Previous 300 | of 38 | Next 300 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!