Crystallography Open Database
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Result: there are 1796 entries in the selection
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Searching journal of publication like 'Chem.Commun.' volume of publication is 51
COD ID ![]() |
Links | Formula ![]() |
Space group ![]() |
Cell parameters | Cell volume ![]() |
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7118105 | CIF | C22 H20 Br2 N2 S2 | C 1 2/c 1 | 21.883; 5.8646; 17.6 90; 109.12; 90 | 2134.1 | Yu Jiang; Run Sun; Qiang Wang; Xiang-Ying Tang; Min Shi Cyclization of sulfide, ether or tertiary amine-tethered N-sulfonyl-1,2,3-triazoles: a facile synthetic protocol for 3-substituted isoquinolines or dihydroisoquinolines Chem.Commun., 2015, 51, 16968 |
7118106 | CIF | C12 H13 N S | P 1 21 1 | 5.9732; 7.2898; 11.9181 90; 100.646; 90 | 510.02 | Yu Jiang; Run Sun; Qiang Wang; Xiang-Ying Tang; Min Shi Cyclization of sulfide, ether or tertiary amine-tethered N-sulfonyl-1,2,3-triazoles: a facile synthetic protocol for 3-substituted isoquinolines or dihydroisoquinolines Chem.Commun., 2015, 51, 16968 |
7118107 | CIF | C23 H21 N O2 S2 | C 1 2/c 1 | 32.732; 9.3213; 12.9047 90; 92.347; 90 | 3934 | Yu Jiang; Run Sun; Qiang Wang; Xiang-Ying Tang; Min Shi Cyclization of sulfide, ether or tertiary amine-tethered N-sulfonyl-1,2,3-triazoles: a facile synthetic protocol for 3-substituted isoquinolines or dihydroisoquinolines Chem.Commun., 2015, 51, 16968 |
7118108 | CIF | C29 H26 N2 O2 S | P 1 21/c 1 | 13.134; 15.776; 12.1965 90; 106.946; 90 | 2417.4 | Yu Jiang; Run Sun; Qiang Wang; Xiang-Ying Tang; Min Shi Cyclization of sulfide, ether or tertiary amine-tethered N-sulfonyl-1,2,3-triazoles: a facile synthetic protocol for 3-substituted isoquinolines or dihydroisoquinolines Chem.Commun., 2015, 51, 16968 |
7118109 | CIF | C27 H20 N2 | P 1 21 1 | 9.9297; 9.6354; 10.6037 90; 90.08; 90 | 1014.53 | Sayani Mukherjee; P. S. Salini; A. Srinivasan; S Peruncheralathan AIEE phenomenon: tetraaryl vs. triaryl pyrazoles Chem.Commun., 2015, 51, 17148 |
7118110 | CIF | C26 H19 N3 | P 1 21 1 | 9.7331; 9.7771; 10.5392 90; 90.204; 90 | 1002.92 | Sayani Mukherjee; P. S. Salini; A. Srinivasan; S Peruncheralathan AIEE phenomenon: tetraaryl vs. triaryl pyrazoles Chem.Commun., 2015, 51, 17148 |
7118111 | CIF | C21 H16 N2 | F d d 2 | 29.627; 36.79; 5.865 90; 90; 90 | 6393 | Sayani Mukherjee; P. S. Salini; A. Srinivasan; S Peruncheralathan AIEE phenomenon: tetraaryl vs. triaryl pyrazoles Chem.Commun., 2015, 51, 17148 |
7118112 | CIF | C23 H17 F7 O2 | P -1 | 13.635; 13.766; 14.405 108.215; 105.015; 110.595 | 2187.4 | Can Xue; Xin Huang; Shangze Wu; Jing Zhou; Jianxin Dai; Chunling Fu; Shengming Ma TfOH-catalyzed domino cycloisomerization/hydrolytic defluorination of 2,3-allenyl perfluoroalkyl ketones Chem.Commun., 2015, 51, 17112 |
7118113 | CIF | C48 H32 Br8 Cu10 N4 O9 | F d d d :2 | 7.9878; 33.9352; 39.1992 90; 90; 90 | 10625.6 | Wei-Hui Fang; Lei Zhang; Jian Zhang; Guo-Yu Yang A highly stable face-extended diamondoid cluster-organic framework incorporating infinite inorganic guests Chem.Commun., 2015, 51, 17174 |
7118114 | CIF | C26 H32 O6 | P 21 21 21 | 7.7711; 11.0137; 12.6885 90; 90; 90 | 1085.99 | Gaoyuan Zhao; Min He; Huilin Li; Shuangshuang Duan; Ziyun Yuan; Xingang Xie; Xuegong She Domino intramolecular Diels-Alder reactions to construct a 6/6/5/5 fused tetracyclic framework Chem.Commun., 2015, 51, 17321 |
7118115 | CIF | C14 H20 O3 | P 1 21 1 | 15.8905; 6.1745; 19.186 90; 104.581; 90 | 1821.8 | Gaoyuan Zhao; Min He; Huilin Li; Shuangshuang Duan; Ziyun Yuan; Xingang Xie; Xuegong She Domino intramolecular Diels-Alder reactions to construct a 6/6/5/5 fused tetracyclic framework Chem.Commun., 2015, 51, 17321 |
7118116 | CIF | C22 H18 Co N4 O4 | P -1 | 8.665; 8.683; 9.769 80.53; 76.38; 76.01 | 688.6 | Yukun Zhao; Junqi Lin; Yongdong Liu; Baochun Ma; Yong Ding; Mindong Chen Efficient light-driven water oxidation catalyzed by a mononuclear cobalt(III) complex Chem.Commun., 2015, 51, 17309 |
7118117 | CIF | C40 H46 N2 S2 | P -1 | 9.4905; 13.4085; 15.1433 77.19; 87.743; 74.954 | 1814.32 | Daisuke Sakamaki; Daisuke Kumano; Eiji Yashim; Shu Seki A double hetero[4]helicene composed of two phenothiazines: synthesis, structural properties, and cationic states Chem.Commun., 2015, 51, 17237 |
7118118 | CIF | C41 H48 Cl8 N2 S2 Sb | P 1 21/c 1 | 11.982; 15.925; 24.598 90; 90.15; 90 | 4694 | Daisuke Sakamaki; Daisuke Kumano; Eiji Yashim; Shu Seki A double hetero[4]helicene composed of two phenothiazines: synthesis, structural properties, and cationic states Chem.Commun., 2015, 51, 17237 |
7118119 | CIF | C41 H52 N2 O S2 | C 1 2/c 1 | 23.0126; 29.0068; 22.0641 90; 104.716; 90 | 14245.1 | Daisuke Sakamaki; Daisuke Kumano; Eiji Yashim; Shu Seki A double hetero[4]helicene composed of two phenothiazines: synthesis, structural properties, and cationic states Chem.Commun., 2015, 51, 17237 |
7118120 | CIF | C46 H62 Cl12 N2 S2 Sb2 | P -1 | 16.337; 20.1317; 20.3767 103.182; 91.496; 112.226 | 5993.2 | Daisuke Sakamaki; Daisuke Kumano; Eiji Yashim; Shu Seki A double hetero[4]helicene composed of two phenothiazines: synthesis, structural properties, and cationic states Chem.Commun., 2015, 51, 17237 |
7118121 | CIF | C84 H132 Cl12 Cu4 Dy4 N28 O48 | P m m n | 19.3834; 27.657; 15.3958 90; 90; 90 | 8253.5 | Jianfeng Wu; Lang Zhao; Mei Guo; Jinkui Tang Constructing supramolecular grids: from 4f square to 3d-4f grid Chem.Commun., 2015, 51, 17317 |
7118122 | CIF | C80 H76 Dy4 F12 N28 O44 S4 | I 41/a m d | 21.384; 21.384; 38.507 90; 90; 90 | 17608 | Jianfeng Wu; Lang Zhao; Mei Guo; Jinkui Tang Constructing supramolecular grids: from 4f square to 3d-4f grid Chem.Commun., 2015, 51, 17317 |
7118123 | CIF | C76 H76 Cl12 Dy4 N28 O16 | P 42/n | 21.9388; 21.9388; 16.335 90; 90; 90 | 7862.2 | Jianfeng Wu; Lang Zhao; Mei Guo; Jinkui Tang Constructing supramolecular grids: from 4f square to 3d-4f grid Chem.Commun., 2015, 51, 17317 |
7118124 | CIF | C14 H4 N O9 Zn2 | I -4 3 m | 28.122; 28.122; 28.122 90; 90; 90 | 22240 | Jia, Yan-Yuan; Zhang, Ying-Hui; Xu, Jian; Feng, Rui; Zhang, Ming-Shi; Bu, Xian-He A high-performance "sweeper" for toxic cationic herbicides: an anionic metal-organic framework with a tetrapodal cage. Chemical communications (Cambridge, England), 2015, 51, 17439-17442 |
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