Crystallography Open Database
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Searching journal of publication like 'Chem.Commun.'
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7133796 | CIF | C81 H38 Al2 F30 N4 P2 | P -1 | 11.2784; 17.5791; 20.1614 94.334; 99.002; 100.389 | 3861.1 | Tang, Beili; Ju, Shaoying; Yan, Weili; Chen, Ting; Stephan, Douglas W.; Wu, Yile Reactivity of <i>N</i>-(isocyanoimino)triphenylphosphorane toward group 13 Lewis acids. Chemical communications (Cambridge, England), 2024, 60, 12932-12935 |
| 7133797 | CIF | C62 H50 Cl3 F4 In N4 P2 | C 1 c 1 | 24.0532; 20.9341; 11.6059 90; 102.431; 90 | 5706.94 | Tang, Beili; Ju, Shaoying; Yan, Weili; Chen, Ting; Stephan, Douglas W.; Wu, Yile Reactivity of <i>N</i>-(isocyanoimino)triphenylphosphorane toward group 13 Lewis acids. Chemical communications (Cambridge, England), 2024, 60, 12932-12935 |
| 7133798 | CIF | C82 H65 Cl12 F Ga4 N8 P4 | P -1 | 17.4641; 17.7994; 17.8166 79.202; 62.982; 61.288 | 4323.8 | Tang, Beili; Ju, Shaoying; Yan, Weili; Chen, Ting; Stephan, Douglas W.; Wu, Yile Reactivity of <i>N</i>-(isocyanoimino)triphenylphosphorane toward group 13 Lewis acids. Chemical communications (Cambridge, England), 2024, 60, 12932-12935 |
| 7133799 | CIF | C50 H25 B2 F20 N2 P | P -1 | 11.9853; 12.0437; 18.347 93.329; 104.396; 115.728 | 2268.7 | Tang, Beili; Ju, Shaoying; Yan, Weili; Chen, Ting; Stephan, Douglas W.; Wu, Yile Reactivity of <i>N</i>-(isocyanoimino)triphenylphosphorane toward group 13 Lewis acids. Chemical communications (Cambridge, England), 2024, 60, 12932-12935 |
| 7133800 | CIF | C81.3 H50.2 Al2 Cl2 F21 N4 P2 | P 1 21/c 1 | 15.3044; 25.9421; 19.9557 90; 109.49; 90 | 7469 | Tang, Beili; Ju, Shaoying; Yan, Weili; Chen, Ting; Stephan, Douglas W.; Wu, Yile Reactivity of <i>N</i>-(isocyanoimino)triphenylphosphorane toward group 13 Lewis acids. Chemical communications (Cambridge, England), 2024, 60, 12932-12935 |
| 7133801 | CIF | Ba2 F2 Ge Se3 | P n m a | 12.8823; 19.118; 6.4566 90; 90; 90 | 1590.2 | Li, Kaixuan; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng Ba<sub>2</sub>GeF<sub>2</sub>Q<sub>3</sub> (Q = S, Se) and Ba<sub>3</sub>GeF<sub>2</sub>Se<sub>4</sub>: new F-based chalcohalides with enhanced birefringence. Chemical communications (Cambridge, England), 2024, 60, 12734-12737 |
| 7133802 | CIF | Ba3 F2 Ge Se4 | P 1 21/n 1 | 9.3777; 9.4571; 12.3301 90; 91.668; 90 | 1093.04 | Li, Kaixuan; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng Ba<sub>2</sub>GeF<sub>2</sub>Q<sub>3</sub> (Q = S, Se) and Ba<sub>3</sub>GeF<sub>2</sub>Se<sub>4</sub>: new F-based chalcohalides with enhanced birefringence. Chemical communications (Cambridge, England), 2024, 60, 12734-12737 |
| 7133803 | CIF | Ba2 F2 Ge S3 | P n m a | 12.626; 18.669; 6.316 90; 90; 90 | 1489 | Li, Kaixuan; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng Ba<sub>2</sub>GeF<sub>2</sub>Q<sub>3</sub> (Q = S, Se) and Ba<sub>3</sub>GeF<sub>2</sub>Se<sub>4</sub>: new F-based chalcohalides with enhanced birefringence. Chemical communications (Cambridge, England), 2024, 60, 12734-12737 |
| 7133804 | CIF | C26 H25 Cl N4 O | P 1 21/n 1 | 7.6248; 10.9476; 26.8702 90; 90.753; 90 | 2242.75 | Qiu, Xujun; Cai, Qianyu; Pohl, Eric; Jung, André; Su, Haopu; Fuhr, Olaf; Schepers, Ute; Bräse, Stefan A simple method to modulate the selectivity of aryl azide photolysis using cucurbit[8]uril. Chemical communications (Cambridge, England), 2024, 60, 12852-12855 |
| 7133805 | CIF | C30 H24 F6 N2 O4 | P 1 21/c 1 | 10.4972; 20.641; 12.7749 90; 106.847; 90 | 2649.18 | Qiu, Xujun; Cai, Qianyu; Pohl, Eric; Jung, André; Su, Haopu; Fuhr, Olaf; Schepers, Ute; Bräse, Stefan A simple method to modulate the selectivity of aryl azide photolysis using cucurbit[8]uril. Chemical communications (Cambridge, England), 2024, 60, 12852-12855 |
| 7133806 | CIF | C27 H26.5 Cl N2.5 O | P 1 21/c 1 | 10.0721; 19.0557; 23.2446 90; 94.802; 90 | 4445.7 | Qiu, Xujun; Cai, Qianyu; Pohl, Eric; Jung, André; Su, Haopu; Fuhr, Olaf; Schepers, Ute; Bräse, Stefan A simple method to modulate the selectivity of aryl azide photolysis using cucurbit[8]uril. Chemical communications (Cambridge, England), 2024, 60, 12852-12855 |
| 7133807 | CIF | C24 H26 Eu N3 O14 | P b c a | 14.0075; 18.751; 20.4381 90; 90; 90 | 5368.2 | Wang, Hao; Sun, Xiao-Han; Wang, Tian-Tian; Li, Yu-Xin; Xu, Ying-Ming; Sun, Wen-Bin Two-dimensional viologen-based lanthanide coordination polymers as multi-stimuli responsive materials to light and amines with a fluorescence response. Chemical communications (Cambridge, England), 2024, 60, 12413-12416 |
| 7133808 | CIF | C24 H26 N3 O14 Tb | P b c a | 14.6366; 18.5358; 19.7866 90; 90; 90 | 5368.13 | Wang, Hao; Sun, Xiao-Han; Wang, Tian-Tian; Li, Yu-Xin; Xu, Ying-Ming; Sun, Wen-Bin Two-dimensional viologen-based lanthanide coordination polymers as multi-stimuli responsive materials to light and amines with a fluorescence response. Chemical communications (Cambridge, England), 2024, 60, 12413-12416 |
| 7133809 | CIF | C3.5 H2.83 Cl0.17 N0 O0.5 S0.33 | P -1 | 8.2512; 11.5639; 11.6055 117.324; 97.055; 94.082 | 966.08 | Barik, Dinabandhu; Chakraborty, Nikita; Sahoo, Ashish K.; Dhara, Hirendra Nath; Patel, Bhisma K. Electron-donor-acceptor (EDA) complex-driven regioselective vicinal and oxidative geminal functionalization of alkynes. Chemical communications (Cambridge, England), 2024, 60, 12577-12580 |
| 7133810 | CIF | C3.33 H2.83 N0.17 O0.33 S0.33 | P n a 21 | 11.753; 8.71; 17.811 90; 90; 90 | 1823.3 | Barik, Dinabandhu; Chakraborty, Nikita; Sahoo, Ashish K.; Dhara, Hirendra Nath; Patel, Bhisma K. Electron-donor-acceptor (EDA) complex-driven regioselective vicinal and oxidative geminal functionalization of alkynes. Chemical communications (Cambridge, England), 2024, 60, 12577-12580 |
| 7133811 | CIF | C24 H22 Cl N5 O2 | P 1 21/c 1 | 16.3613; 6.8967; 19.5442 90; 103.785; 90 | 2141.83 | Qiu, Xujun; Pohl, Eric; Jung, André; Cai, Qianyu; Su, Haopu; Fuhr, Olaf; Schepers, Ute; Bräse, Stefan Modulating the photolysis of aryl azides in a supramolecular host to develop photoactivatable fluorophores. Chemical communications (Cambridge, England), 2024, 60, 12856-12859 |
| 7133812 | CIF | C24 H25 Cl N5 O2.5 | P -1 | 9.5693; 10.1473; 24.8566 101.497; 93.876; 103.476 | 2283.56 | Qiu, Xujun; Pohl, Eric; Jung, André; Cai, Qianyu; Su, Haopu; Fuhr, Olaf; Schepers, Ute; Bräse, Stefan Modulating the photolysis of aryl azides in a supramolecular host to develop photoactivatable fluorophores. Chemical communications (Cambridge, England), 2024, 60, 12856-12859 |
| 7133813 | CIF | C21 H22 Cl Cu N2 S | P 21 21 21 | 8.5644; 9.6993; 23.7155 90; 90; 90 | 1970.02 | Saha, Ratnakar; Maharana, Suraj Kumar; Jana, Narayan Ch; Bagh, Bidraha Copper-catalyzed C(sp<sup>3</sup>)-H alkylation of fluorene with primary and secondary alcohols using a borrowing hydrogen method. Chemical communications (Cambridge, England), 2024, 60, 10144-10147 |
| 7133814 | CIF | C325 H504 Cr14 Cu4 F16 N6 Ni2 O86 S2 | P -1 | 16.506; 34.2036; 35.1533 80.444; 88.909; 85.438 | 19508.6 | Lockyer, Selena J.; Whitehead, George F. S.; Timco, Grigore A.; McInnes, Eric J. L.; Winpenny, Richard E. P. One-, two- and three-dimensional interlocked polymers based on hybrid inorganic-organic rotaxanes. Chemical communications (Cambridge, England), 2024, 60, 10124-10127 |
| 7133815 | CIF | C170.2 H290.65 Cr7 Cu4 F8 N5 Ni O61.2 | P 1 21/n 1 | 26.8191; 19.6641; 43.9326 90; 104.391; 90 | 22441.9 | Lockyer, Selena J.; Whitehead, George F. S.; Timco, Grigore A.; McInnes, Eric J. L.; Winpenny, Richard E. P. One-, two- and three-dimensional interlocked polymers based on hybrid inorganic-organic rotaxanes. Chemical communications (Cambridge, England), 2024, 60, 10124-10127 |
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