Crystallography Open Database
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Result: there are 831 entries in the selection
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Searching journal of publication like 'Chem. Sci.' volume of publication is 6
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1520452 | CIF | C24 H17 N4 O | P 1 21/n 1 | 3.9114; 20.5945; 22.458 90; 91.758; 90 | 1808.2 | Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido Profluorescent verdazyl radicals ‒ synthesis and characterization Chem. Sci., 2015, 6, 4712 |
| 1520453 | CIF | C28 H19 N4 O | P 1 21 1 | 11.7763; 5.828; 16.1543 90; 104.773; 90 | 1072.06 | Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido Profluorescent verdazyl radicals ‒ synthesis and characterization Chem. Sci., 2015, 6, 4712 |
| 1520454 | CIF | C32 H26 N4 O | P 1 21/c 1 | 7.474; 9.2641; 35.865 90; 91.227; 90 | 2482.7 | Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido Profluorescent verdazyl radicals ‒ synthesis and characterization Chem. Sci., 2015, 6, 4712 |
| 1520455 | CIF | C36 H28 N4 O | P 1 21/c 1 | 11.2158; 10.0647; 24.8459 90; 97.414; 90 | 2781.25 | Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido Profluorescent verdazyl radicals ‒ synthesis and characterization Chem. Sci., 2015, 6, 4712 |
| 1520456 | CIF | C21 H17 Br F3 N O2 | P 21 21 21 | 9.1964; 13.4028; 15.611 90; 90; 90 | 1924.2 | Zhang, Xiao; Liu, Wen-Bo; Tu, Hang-Fei; You, Shu-Li Ligand-enabled Ir-catalyzed intermolecular diastereoselective and enantioselective allylic alkylation of 3-substituted indoles Chem. Sci., 2015, 6, 4525 |
| 1520493 | CIF | C30 H26 Co F6 N6 O7 S2 | P -1 | 11.0341; 12.5779; 13.0044 82.865; 88.796; 66.687 | 1643.85 | Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J. Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water Chem. Sci., 2015, 6, 4954 |
| 1520494 | CIF | C29 H35 F6 N7 O12 S2 Zn | P 1 21/n 1 | 13.0156; 12.7488; 22.3963 90; 92.294; 90 | 3713.3 | Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J. Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water Chem. Sci., 2015, 6, 4954 |
| 1520495 | CIF | C36 H42 Co F6 N6 O11 S2 | P 1 21/n 1 | 12.4657; 15.6171; 21.316 90; 91.047; 90 | 4149.1 | Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J. Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water Chem. Sci., 2015, 6, 4954 |
| 1520496 | CIF | C30 H30 F6 N6 O11 S2 Zn | P -1 | 14.707; 21.388; 25.657 67.683; 75.282; 89.683 | 7184 | Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J. Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water Chem. Sci., 2015, 6, 4954 |
| 1520497 | CIF | C30 H32.5 F6 N6 O10 S2 Zn | P -1 | 11.0677; 13.3087; 13.5558 71.591; 78.668; 67.235 | 1740.65 | Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J. Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water Chem. Sci., 2015, 6, 4954 |
| 1520498 | CIF | C29 H27.5 Co F6 N7 O9.25 S2 | P -1 | 13.2461; 20.9848; 26.9609 111.361; 96.713; 94.455 | 6872.7 | Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J. Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water Chem. Sci., 2015, 6, 4954 |
| 1520524 | CIF | C53 H69 N6 O25 P2 Ru | P n n a | 21.3561; 19.4016; 14.9635 90; 90; 90 | 6200.01 | Fielden, John; Sumliner, Jordan M.; Han, Nannan; Geletii, Yurii V.; Xiang, Xu; Musaev, Djamaladdin G.; Lian, Tianquan; Hill, Craig L. Water splitting with polyoxometalate-treated photoanodes: enhancing performance through sensitizer design Chem. Sci., 2015, 6, 5531 |
| 1520525 | CIF | C34 H20 Co2 N2 O8 | P -1 | 12.956; 13.122; 13.752 84.973; 67.595; 83.245 | 2144.1 | Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J. Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework Chem. Sci., 2015, 6, 4986 |
| 1520526 | CIF | C17 H10 Co N O4 | P -1 | 7.7116; 10.2889; 11.0085 71.43; 86.282; 82.265 | 820.22 | Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J. Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework Chem. Sci., 2015, 6, 4986 |
| 1520527 | CIF | C34 H20 Co2 N2 O8 | P -1 | 12.9698; 13.1304; 13.7579 85.041; 68.014; 83.544 | 2156.3 | Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J. Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework Chem. Sci., 2015, 6, 4986 |
| 1520528 | CIF | C17 H10 Co N O4 | P -1 | 7.6397; 10.4311; 10.9968 71.121; 87.061; 83.361 | 823.5 | Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J. Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework Chem. Sci., 2015, 6, 4986 |
| 1520529 | CIF | C51 H30 Co3 N3 O12 | C 1 2 1 | 17.173; 19.784; 13.887 90; 95.771; 90 | 4694 | Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J. Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework Chem. Sci., 2015, 6, 4986 |
| 1520530 | CIF | C51 H30 Co3 N3 O12 | C 1 2 1 | 17.0391; 20.0278; 13.8334 90; 96.243; 90 | 4692.7 | Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J. Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework Chem. Sci., 2015, 6, 4986 |
| 1520535 | CIF | C41 H46 N4 S2 | C 1 2/c 1 | 24.1082; 18.137; 16.7624 90; 106.002; 90 | 7045.4 | Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L. Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation Chem. Sci., 2015, 6, 5144 |
| 1520536 | CIF | C65 H64 B2 N4 S2 | I 41/a :2 | 41.594; 41.594; 13.1413 90; 90; 90 | 22735.2 | Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L. Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation Chem. Sci., 2015, 6, 5144 |
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