Crystallography Open Database
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Result: there are 165 entries in the selection
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Searching journal of publication like 'Chemical communications (Cambridge, England)' volume of publication is 58
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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7129722 | CIF | C20 H21 Cu N O6 | P -1 | 9.8246; 13.603; 14.5457 83.192; 85.269; 88.081 | 1923.11 | Reichle, Alexander; Sterzel, Hannes; Kreitmeier, Peter; Fayad, Remi; Castellano, Felix N.; Rehbein, Julia; Reiser, Oliver Copper(II)-photocatalyzed decarboxylative oxygenation of carboxylic acids. Chemical communications (Cambridge, England), 2022, 58, 4456-4459 |
7129741 | CIF | C24 H28 Au B Cl P | P 1 21/c 1 | 17.1732; 13.6458; 19.7945 90; 95.133; 90 | 4620.1 | Krämer, Felix; Radius, Michael; Berberich, Helga; Fernández, Israel; Breher, Frank A neutral, acyclic, borataalkene-like ligand for group 11 metals: L- and Z-type ligands side by side. Chemical communications (Cambridge, England), 2022, 58, 3905-3908 |
7129743 | CIF | C28 H26 Cu2 I2 N5 | C m c m | 13.439; 28.091; 9.4068 90; 90; 90 | 3551.2 | Zhong, Bingwen; Huang, Huilin; Jing, Xu; Duan, Chunying Binuclear copper iodine cluster-based coordination sheets as photocatalysts for decarboxylative cyanation. Chemical communications (Cambridge, England), 2022, 58, 3961-3964 |
7129744 | CIF | C98 H87 Cu6 I6 N13 O2 | P -1 | 13.3961; 15.0316; 33.541 91.323; 97.137; 114.728 | 6066 | Zhong, Bingwen; Huang, Huilin; Jing, Xu; Duan, Chunying Binuclear copper iodine cluster-based coordination sheets as photocatalysts for decarboxylative cyanation. Chemical communications (Cambridge, England), 2022, 58, 3961-3964 |
7129755 | CIF | C22 H27 B F2 N2 O6 P2 | P 1 21/c 1 | 14.4985; 15.0627; 11.9448 90; 107.78; 90 | 2483.99 | Lv, Fan; Li, Heng; Wu, Qinghua; Guo, Xing; Zhang, Hongtao; Yu, Changjiang; Jiao, Lijuan; Hao, Erhong Silver-mediated, direct phosphorylation of BODIPY dyes at the 3- or 3,5-positions with H-phosphonates. Chemical communications (Cambridge, England), 2022, 58, 3937-3940 |
7129758 | CIF | C40 H38 N2 O | P -1 | 11.3021; 11.3449; 15.1031 89.431; 68.393; 64.454 | 1598.7 | Yu, Bangkui; Huang, Renbin; Li, Renren; Zhang, Haocheng; Huang, Hanmin Silver-catalyzed chemodivergent assembly of aminomethylated isochromenes and naphthols. Chemical communications (Cambridge, England), 2022, 58, 3969-3972 |
7129759 | CIF | C40 H38 N2 O | P -1 | 12.1191; 12.6465; 12.9053 96.455; 115.408; 109.434 | 1607.44 | Yu, Bangkui; Huang, Renbin; Li, Renren; Zhang, Haocheng; Huang, Hanmin Silver-catalyzed chemodivergent assembly of aminomethylated isochromenes and naphthols. Chemical communications (Cambridge, England), 2022, 58, 3969-3972 |
7129760 | CIF | C44 H40 N2 O | P 1 21/n 1 | 9.8246; 16.0677; 21.9664 90; 91.832; 90 | 3465.82 | Yu, Bangkui; Huang, Renbin; Li, Renren; Zhang, Haocheng; Huang, Hanmin Silver-catalyzed chemodivergent assembly of aminomethylated isochromenes and naphthols. Chemical communications (Cambridge, England), 2022, 58, 3969-3972 |
7129781 | CIF | C22 H17 F O4 S | P 1 21 1 | 8.3425; 24.9386; 9.474 90; 99.117; 90 | 1946.17 | Zhu, Zhou-Hao; Ding, Yi-Xuan; Zhou, Yong-Gui Transfer-catalyst-free biomimetic asymmetric reduction of 3-sulfonyl coumarins with a regenerable NAD(P)H model. Chemical communications (Cambridge, England), 2022, 58, 3973-3976 |
7129785 | CIF | C13 H23 B Cl N Si | P 1 21/c 1 | 8.256; 11.579; 16.616 90; 103.076; 90 | 1547.2 | Maier, Matthias; Klopf, Jonas; Glasmacher, Clemens; Fantuzzi, Felipe; Bachmann, Jonas; Ayhan, Ozan; Koner, Abhishek; Engels, Bernd; Helten, Holger Electrophilic activation of difunctional aminoboranes: B-N coupling <i>versus</i> intramolecular Cl/Me exchange. Chemical communications (Cambridge, England), 2022, 58, 4464-4467 |
7129804 | CIF | C66 H66 N7 O19 Zn3 | P 1 21/c 1 | 25.909; 17.361; 17.014 90; 93.9; 90 | 7635 | Thoonen, Shannon; Tay, Hui Min; Hua, Carol A chiral binaphthyl-based coordination polymer as an enantioselective fluorescence sensor. Chemical communications (Cambridge, England), 2022, 58, 4512-4515 |
7129807 | CIF | C72 H135 Mo N Na O12 P2 Si3 U | P -1 | 13.6525; 16.4788; 19.2469 81.3024; 79.5672; 82.5868 | 4186.48 | Barluzzi, Luciano; Jori, Nadir; He, Tianyi; Rajeshkumar, Thayalan; Scopelliti, Rosario; Maron, Laurent; Oyala, Paul; Agapie, Theodor; Mazzanti, Marinella Heterometallic uranium/molybdenum nitride synthesis <i>via</i> partial N-atom transfer. Chemical communications (Cambridge, England), 2022, 58, 4655-4658 |
7129824 | CIF | C12 H10 Cd1.493 Cl O2 S2 | P 1 21/c 1 | 16.5869; 11.9546; 14.0741 90; 109.534; 90 | 2630.1 | Pan, Yu; Wang, Chengpeng; Fu, Zhihua; Wang, Guang-E; Xu, Gang Fluorescence sensing of nitrophenol explosives using a two-dimensional organic-metal chalcogenide fully covered with functional groups. Chemical communications (Cambridge, England), 2022, 58, 4615-4618 |
7129828 | CIF | C16 H21 Cl2 Mn N3 O10 | P -1 | 8.906; 9.306; 14.498 89.499; 76.65; 65.347 | 1057.3 | Jeon, Hyeri; Kim, Jisoo; Kim, Jin; Cho, Kyung-Bin; Hong, Seungwoo An end-on bis(μ-hydroxido) dimanganese(II,III) azide complex for C-H bond and O-H bond activation reactions. Chemical communications (Cambridge, England), 2022, 58, 4623-4626 |
7129829 | CIF | C32 H42 Mn2 N18 O4 | P 1 21/c 1 | 10.8912; 10.4204; 16.9841 90; 99.8018; 90 | 1899.4 | Jeon, Hyeri; Kim, Jisoo; Kim, Jin; Cho, Kyung-Bin; Hong, Seungwoo An end-on bis(μ-hydroxido) dimanganese(II,III) azide complex for C-H bond and O-H bond activation reactions. Chemical communications (Cambridge, England), 2022, 58, 4623-4626 |
7129830 | CIF | C29 H27 N2 O8 Tb | P -1 | 9.397; 10.471; 15.004 73.416; 78.485; 66.927 | 1295.3 | Wang, Xiaomei; Liu, Cheng; Wang, Ming; Zhou, Xinhui; You, Yujian; Xiao, Hongping A selective fluorescence turn-on sensing coordination polymer for antibiotic aztreonam. Chemical communications (Cambridge, England), 2022, 58, 4667-4670 |
7129831 | CIF | C29 H28 Cl N O4 | P -1 | 10.0582; 11.3137; 11.3744 85.422; 89.974; 77.443 | 1259.17 | Yao, Tuanli; Zhao, Shuaijing; Liu, Tao; Wu, Yuting; Ma, Yanhui; Li, Tao; Qin, Xiangyang Transition-metal-free approaches to 2,3-diarylated indenones from 2-alkynylbenzaldehydes and phenols with tunable selectivity. Chemical communications (Cambridge, England), 2022, 58, 4592-4595 |
7129832 | CIF | C30 H28 F3 N O4 | C 1 2/c 1 | 25.52; 11.215; 20.049 90; 112.806; 90 | 5290 | Yao, Tuanli; Zhao, Shuaijing; Liu, Tao; Wu, Yuting; Ma, Yanhui; Li, Tao; Qin, Xiangyang Transition-metal-free approaches to 2,3-diarylated indenones from 2-alkynylbenzaldehydes and phenols with tunable selectivity. Chemical communications (Cambridge, England), 2022, 58, 4592-4595 |
7129833 | CIF | C32 H33 F O4 | P -1 | 10.7537; 11.4253; 11.8372 83.875; 77.861; 68.433 | 1321.6 | Yao, Tuanli; Zhao, Shuaijing; Liu, Tao; Wu, Yuting; Ma, Yanhui; Li, Tao; Qin, Xiangyang Transition-metal-free approaches to 2,3-diarylated indenones from 2-alkynylbenzaldehydes and phenols with tunable selectivity. Chemical communications (Cambridge, England), 2022, 58, 4592-4595 |
7129834 | CIF | C32 H33 Cl O4 | P -1 | 9.1084; 11.8341; 13.8157 94.809; 107.322; 91.397 | 1414.74 | Yao, Tuanli; Zhao, Shuaijing; Liu, Tao; Wu, Yuting; Ma, Yanhui; Li, Tao; Qin, Xiangyang Transition-metal-free approaches to 2,3-diarylated indenones from 2-alkynylbenzaldehydes and phenols with tunable selectivity. Chemical communications (Cambridge, England), 2022, 58, 4592-4595 |
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