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 | Bibliography |
---|---|---|---|---|---|---|
7116659 | CIF | C15 H22 B F N2 | P -1 | 7.486; 9.564; 10.597 75.8; 76.99; 75.35 | 700.8 | Masahito Murai; Tetsuya Omura; Yoichiro Kuninobu; Kazuhiko Takai Rhenium-catalysed dehydrogenative borylation of primary and secondary C(sp^3^)-H bonds adjacent to a nitrogen atom Chem.Commun., 2015, 51, 4583 |
7116660 | CIF | C46 H79 Fe9 N2 O50 | P 32 2 1 | 18.927; 18.927; 24.693 90; 90; 120 | 7661 | Jiong-Peng Zhao; Song-De Han; Xue Jiang; Jian Xu; Ze Chang; Xian-He Bu A three dimensional magnetically frustrated metal-organic framework via the vertices augmentation of underlying net Chem.Commun., 2015, 51, 4627 |
7116661 | CIF | C H N O | P 21 21 21 | 10.5611; 15.5632; 22.4083 90; 90; 90 | 3683.1 | Pei-Qiang Huang; Su-Yu Huang; Long-Hui Gao; Zhong-Yi Mao; Zong Chang; Ai-E Wang Enantioselective total synthesis of (+)-methoxystemofoline and (+)-isomethoxystemofoline Chem.Commun., 2015, 51, 4576 |
7116662 | CIF | C70 H110 Li2 O2 Pb2 Si4 | P -1 | 12.2658; 16.7325; 20.375 99.254; 107.15; 107.882 | 3654.6 | Masaichi Saito; Marisa Nakada; Takuya Kuwabara; Mao Minoura A reversible two-electron redox system involving a divalent lead species Chem.Commun., 2015, 51, 4674 |
7116663 | CIF | C36 H56 Li2 O2 Pb Si2 | P -1 | 12.4117; 12.4449; 13.7628 82.874; 67.352; 75.447 | 1898.1 | Masaichi Saito; Marisa Nakada; Takuya Kuwabara; Mao Minoura A reversible two-electron redox system involving a divalent lead species Chem.Commun., 2015, 51, 4674 |
7116664 | CIF | C16 H17 N O2 S | P 1 21/n 1 | 14.3451; 5.6024; 19.171 90; 110.01; 90 | 1447.7 | Xiang-Wei Liu; Jiang-Ling Shi; Jiang-Bo Wei; Chao Yang; Jia-Xuan Yan; Kun Peng; Le Dai; Chen-Guang Li; Bi-Qin Wang; Zhang-Jie Shi Diversified syntheses of multifunctionalized thiazole derivatives via regioselective and programmed C-H activation Chem.Commun., 2015, 51, 4599 |
7116665 | CIF | Fe1.172 H Li0.828 O S | P 4/n m m :1 | 3.7038; 3.7038; 8.8852 90; 90; 90 | 121.888 | U. Pachmayr; D. Johrendt [(Li0.8Fe0.2)OH]FeS and the ferromagnetic superconductors [(Li0.8Fe0.2)OH]Fe(S1-xSex) (0 < x ? 1) Chem.Commun., 2015, 51, 4689 |
7116666 | CIF | C148 H96 Mn6 N20 O18 | P 1 21/c 1 | 27.159; 13.925; 41.043 90; 112.375; 90 | 14353 | L. A. Barrios; J. Salinas-Uber; O. Roubeau; S. J. Teat; G. Aromi Molecular self-recognition: a chiral [Mn(II)6] wheel via donor-acceptor pi^...^pi contacts and H-bonds Chem.Commun., 2015, 51, 4631 |
7116667 | CIF | C49 H62 N6 O3 | P 1 21/n 1 | 14.623; 16.641; 18.326 90; 101.777; 90 | 4365.6 | L. A. Barrios; J. Salinas-Uber; O. Roubeau; S. J. Teat; G. Aromi Molecular self-recognition: a chiral [Mn(II)6] wheel via donor-acceptor pi^...^pi contacts and H-bonds Chem.Commun., 2015, 51, 4631 |
7116668 | CIF | C72 H96 O Si4 | P 21 21 21 | 13.7114; 19.2562; 25.0769 90; 90; 90 | 6621 | Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene Chem.Commun., 2015, 51, 4607 |
7116669 | CIF | C72 H98 O2 Si4 | P 1 21/c 1 | 13.426; 18.425; 28.086 90; 94.327; 90 | 6928 | Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene Chem.Commun., 2015, 51, 4607 |
7116670 | CIF | C67.2 H91.2 N1.6 O2.4 Si3.2 | P 1 21/c 1 | 13.31; 29.8304; 19.4965 90; 93.59; 90 | 7725.8 | Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene Chem.Commun., 2015, 51, 4607 |
7116671 | CIF | C72 H96 O Si4 | P 1 21/c 1 | 19.768; 21.986; 16.67 90; 111.807; 90 | 6727 | Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene Chem.Commun., 2015, 51, 4607 |
7116672 | CIF | C72 H98 O2 Si4 | P -1 | 13.171; 14.918; 17.544 85.743; 79.779; 84.496 | 3371 | Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene Chem.Commun., 2015, 51, 4607 |
7116688 | CIF | C29 H28 Cl2 N P Ru S | P 1 21/n 1 | 12.6476; 11.7959; 18.6459 90; 102.933; 90 | 2711.21 | Zhang, Hui-Jun; Lin, Weidong; Wu, Zhengjian; Ruan, Wenqing; Wen, Ting-Bin Silver-mediated direct phosphorylation of benzothiazoles and thiazoles with diarylphosphine oxides. Chemical communications (Cambridge, England), 2015, 51, 3450-3453 |
7116689 | CIF | C15 H12 N O P S | C 1 2/c 1 | 10.4363; 13.1058; 20.7087 90; 96.816; 90 | 2812.44 | Zhang, Hui-Jun; Lin, Weidong; Wu, Zhengjian; Ruan, Wenqing; Wen, Ting-Bin Silver-mediated direct phosphorylation of benzothiazoles and thiazoles with diarylphosphine oxides. Chemical communications (Cambridge, England), 2015, 51, 3450-3453 |
7116702 | CIF | C27 H22 N4 O8 Zn | P 1 21/c 1 | 11.361; 15.532; 16.269 90; 94.661; 90 | 2861.3 | Bappaditya Gole; Udishnu Sanyal; Partha Sarathi Mukherjee A smart approach to achieve an exceptionally high loading of metal nanoparticles supported by functionalized extended frameworks for efficient catalysis Chem.Commun., 2015, 51, 4872 |
7116703 | CIF | C23 H14 N2 O5 Zn | C 1 2/c 1 | 29.971; 16.271; 15.804 90; 115.749; 90 | 6942 | Bappaditya Gole; Udishnu Sanyal; Partha Sarathi Mukherjee A smart approach to achieve an exceptionally high loading of metal nanoparticles supported by functionalized extended frameworks for efficient catalysis Chem.Commun., 2015, 51, 4872 |
7116706 | CIF | C25 H24 N2 O | P -1 | 9.491; 9.5574; 10.9648 91.766; 93.926; 97.631 | 982.69 | Subban Kathiravan; Shishir Ghosh; Graeme Hogarth; Ian A. Nicholls Copper catalysed amidation of aryl halides through chelation assistance Chem.Commun., 2015, 51, 4834 |
7116707 | CIF | C19 H20 N2 O S | P 1 21/c 1 | 16.8737; 9.68667; 10.28958 90; 96.9165; 90 | 1669.59 | Subban Kathiravan; Shishir Ghosh; Graeme Hogarth; Ian A. Nicholls Copper catalysed amidation of aryl halides through chelation assistance Chem.Commun., 2015, 51, 4834 |
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