Crystallography Open Database

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Searching journal of publication like 'Chemical communications (Cambridge, England)' volume of publication is 46

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7113049 CIFC19 H13 Br Fe O2P 1 21/a 17.5434; 14.7364; 13.8726
90; 99.146; 90
1522.5Monserrat, Jean-Philippe; Chabot, Guy G.; Hamon, Louis; Quentin, Lionel; Scherman, Daniel; Jaouen, Gérard; Hillard, Elizabeth A.
Synthesis of cytotoxic ferrocenyl flavones via a ferricenium-mediated 1,6-oxidative cyclization.
Chemical communications (Cambridge, England), 2010, 46, 5145-5147
7113050 CIFC26 H34P 1 21/n 17.8785; 17.1725; 8.2929
90; 117.057; 90
999.18Williams, Kyle A.; Bielawski, Christopher W.
Cerberus-type N-heterocyclic carbenes: synthesis and study of the first tritopic carbenes with D(3h)-symmetry.
Chemical communications (Cambridge, England), 2010, 46, 5166-5168
7113051 CIFC32 H38C 1 2/c 169.417; 8.3391; 33.478
90; 117.24; 90
17230Williams, Kyle A.; Bielawski, Christopher W.
Cerberus-type N-heterocyclic carbenes: synthesis and study of the first tritopic carbenes with D(3h)-symmetry.
Chemical communications (Cambridge, England), 2010, 46, 5166-5168
7113052 CIFC107 H134 N6P n m a27.7357; 20.3898; 16.5894
90; 90; 90
9381.7Williams, Kyle A.; Bielawski, Christopher W.
Cerberus-type N-heterocyclic carbenes: synthesis and study of the first tritopic carbenes with D(3h)-symmetry.
Chemical communications (Cambridge, England), 2010, 46, 5166-5168
7113053 CIFC71 H98 N6 S3P n m a23.074; 19.486; 14.463
90; 90; 90
6502.9Williams, Kyle A.; Bielawski, Christopher W.
Cerberus-type N-heterocyclic carbenes: synthesis and study of the first tritopic carbenes with D(3h)-symmetry.
Chemical communications (Cambridge, England), 2010, 46, 5166-5168
7113054 CIFC15 H17 N O2P 1 21/c 14.9255; 19.517; 13.661
90; 93.474; 90
1310.8Zhao, Yu-Long; Yang, Shao-Chun; Di, Chong-Hui; Han, Xiao-Dan; Liu, Qun
Highly efficient synthesis of 3-amino-/alkylthio-cyclobut-2-en-1-ones based on the cyclization of acyl ketene dithioacetals.
Chemical communications (Cambridge, England), 2010, 46, 7614-7616
7113055 CIFC33 H30 Cl N O7 S2P -19.6853; 10.361; 16.908
98.959; 94.333; 117.259
1468.9Chua, Pei Juan; Tan, Bin; Yang, Limin; Zeng, Xiaofei; Zhu, Di; Zhong, Guofu
Highly stereoselective synthesis of indanes with four stereogenic centers via sequential Michael reaction and [3+2] cycloaddition.
Chemical communications (Cambridge, England), 2010, 46, 7611-7613
7113056 CIFC28 H29 Cl N6 O2 RuP -19.1223; 10.4936; 14.8426
79.785; 86.546; 72.825
1335.9Leung, Chi-Fai; Yiu, Shek-Man; Xiang, Jing; Lau, Tai-Chu
Addition of [CH(CN)2]- and [TCNE]˙- to Ru(VI)≡N bearing 8-quinolinolato ligands.
Chemical communications (Cambridge, England), 2010, 46, 7575-7577
7113057 CIFC22.5 H19.75 N5 O3.88 RuI -431.568; 31.568; 11.1516
90; 90; 90
11113Leung, Chi-Fai; Yiu, Shek-Man; Xiang, Jing; Lau, Tai-Chu
Addition of [CH(CN)2]- and [TCNE]˙- to Ru(VI)≡N bearing 8-quinolinolato ligands.
Chemical communications (Cambridge, England), 2010, 46, 7575-7577
7113058 CIFC25 H23.75 N4 O5.88 RuP 1 21/n 115.2068; 18.9057; 17.7568
90; 104.068; 90
4951.89Leung, Chi-Fai; Yiu, Shek-Man; Xiang, Jing; Lau, Tai-Chu
Addition of [CH(CN)2]- and [TCNE]˙- to Ru(VI)≡N bearing 8-quinolinolato ligands.
Chemical communications (Cambridge, England), 2010, 46, 7575-7577
7113059 CIFC24 H23 Br N2 O6P 1 21/c 113.396; 6.8114; 24.048
90; 90.825; 90
2194Lu, Yimin; Geib, Steven J.; Damodaran, Krishnan; Sui, Bin; Zhang, Zijuan; Curran, Dennis P.; Zhang, Wei
Fluorous diastereomeric mixture synthesis (FDMS) of hydantoin-fused hexahydrochromeno[4,3-b]pyrroles.
Chemical communications (Cambridge, England), 2010, 46, 7578-7580
7113060 CIFC12 H48 B4 N5 Sc Si2P 1 21/c 18.3019; 28.6721; 11.4062
90; 108.784; 90
2570.45Hill, Michael S.; Kociok-Köhn, Gabriele; Robinson, Thomas P.
Group 3-centred dehydrocoupling of Me2NH·BH3.
Chemical communications (Cambridge, England), 2010, 46, 7587-7589
7113061 CIFC33 H38 Au Cl N2P 1 21 112.074; 11.168; 22.31
90; 93.82; 90
3002Hirsch-Weil, Dimitri; Abboud, Khalil A.; Hong, Sukwon
Isoquinoline-based chiral monodentate N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2010, 46, 7525-7527
7113062 CIFC27 H32 Au Cl N2P 21 21 219.4129; 16.729; 17.6201
90; 90; 90
2774.6Hirsch-Weil, Dimitri; Abboud, Khalil A.; Hong, Sukwon
Isoquinoline-based chiral monodentate N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2010, 46, 7525-7527
7113063 CIFC9 H6 N O4 ZnP 1 21/a 113.3226; 11.3815; 13.9942
90; 105.746; 90
2042.3Fujii, Kotaro; Lazuen Garay, Ana; Hill, Janeen; Sbircea, Elena; Pan, Zhigang; Xu, Mingcan; Apperley, David C.; James, Stuart L.; Harris, Kenneth D. M.
Direct structure elucidation by powder X-ray diffraction of a metal-organic framework material prepared by solvent-free grinding.
Chemical communications (Cambridge, England), 2010, 46, 7572-7574
7113064 CIFC39 H47 Mo N16 Ni2 S7P 1 21 110.3601; 23.0402; 10.9979
90; 108.947; 90
2482.95Mousavi, Maliheh; Béreau, Virgine; Desplanches, Cédric; Duhayon, Carine; Sutter, Jean-Pascal
Substantial exchange coupling for {Mo-NCS-M} combination: illustration for 1-D [{Mo(NCS)6}{NiL}2(NCS)]n.
Chemical communications (Cambridge, England), 2010, 46, 7519-7521
7113065 CIFC82 H66 Mo N8 P3 S6P 112.9236; 13.2332; 25.9506
88.192; 79.845; 62.372
3864Mousavi, Maliheh; Béreau, Virgine; Desplanches, Cédric; Duhayon, Carine; Sutter, Jean-Pascal
Substantial exchange coupling for {Mo-NCS-M} combination: illustration for 1-D [{Mo(NCS)6}{NiL}2(NCS)]n.
Chemical communications (Cambridge, England), 2010, 46, 7519-7521
7113066 CIFC39 H47 Cr N16 Ni2 S7P 1 21 110.3765; 23.1054; 11.1193
90; 109.15; 90
2518.4Mousavi, Maliheh; Béreau, Virgine; Desplanches, Cédric; Duhayon, Carine; Sutter, Jean-Pascal
Substantial exchange coupling for {Mo-NCS-M} combination: illustration for 1-D [{Mo(NCS)6}{NiL}2(NCS)]n.
Chemical communications (Cambridge, England), 2010, 46, 7519-7521
7113067 CIFC82 H23 Cl2 N O2P 1 21 110.136; 13.5421; 17.233
90; 98.169; 90
2341.4Lincker, Frédéric; Bourgun, Philippe; Stoeckli-Evans, Helen; Saez, Isabel M.; Goodby, John W.; Deschenaux, Robert
Optically active liquid-crystalline fullerodendrimers from enantiomerically pure fulleropyrrolidines.
Chemical communications (Cambridge, England), 2010, 46, 7522-7524
7113068 CIFC10 H5 Cu O5R -3 m :H18.2386; 18.2386; 42.049
90; 90; 120
12113.5Zhao, Dan; Yuan, Daqiang; Yakovenko, Andrey; Zhou, Hong-Cai
A NbO-type metal-organic framework derived from a polyyne-coupled di-isophthalate linker formed in situ.
Chemical communications (Cambridge, England), 2010, 46, 4196-4198

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