Crystallography Open Database
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Searching journal of publication like 'Chemical science' volume of publication is 11
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1556719 | CIF | C21 H19 N O S | P -1 | 7.2702; 8.7819; 13.6782 98.564; 100.026; 104.633 | 814.84 | Ho, Hon Eong; Pagano, Angela; Rossi-Ashton, James A.; Donald, James R.; Epton, Ryan G.; Churchill, Jonathan C.; James, Michael J.; O'Brien, Peter; Taylor, Richard J. K.; Unsworth, William P. Visible-light-induced intramolecular charge transfer in the radical spirocyclisation of indole-tethered ynones Chemical Science, 2020, 11, 1353-1360 |
| 1556720 | CIF | C18 H13 N O | P 1 21/c 1 | 11.42288; 8.41061; 28.0872 90; 100.454; 90 | 2653.64 | Ho, Hon Eong; Pagano, Angela; Rossi-Ashton, James A.; Donald, James R.; Epton, Ryan G.; Churchill, Jonathan C.; James, Michael J.; O'Brien, Peter; Taylor, Richard J. K.; Unsworth, William P. Visible-light-induced intramolecular charge transfer in the radical spirocyclisation of indole-tethered ynones Chemical Science, 2020, 11, 1353-1360 |
| 1556721 | CIF | C24 H19 N O S | P 21 21 21 | 5.81156; 17.547; 18.1227 90; 90; 90 | 1848.07 | Ho, Hon Eong; Pagano, Angela; Rossi-Ashton, James A.; Donald, James R.; Epton, Ryan G.; Churchill, Jonathan C.; James, Michael J.; O'Brien, Peter; Taylor, Richard J. K.; Unsworth, William P. Visible-light-induced intramolecular charge transfer in the radical spirocyclisation of indole-tethered ynones Chemical Science, 2020, 11, 1353-1360 |
| 1556722 | CIF | C19 H15 N O | P 21 21 21 | 7.4225; 9.90594; 19.5109 90; 90; 90 | 1434.57 | Ho, Hon Eong; Pagano, Angela; Rossi-Ashton, James A.; Donald, James R.; Epton, Ryan G.; Churchill, Jonathan C.; James, Michael J.; O'Brien, Peter; Taylor, Richard J. K.; Unsworth, William P. Visible-light-induced intramolecular charge transfer in the radical spirocyclisation of indole-tethered ynones Chemical Science, 2020, 11, 1353-1360 |
| 1556723 | CIF | C25 H21 N O S | P -1 | 8.7543; 9.971; 11.6327 81.846; 74.281; 81.076 | 960.27 | Ho, Hon Eong; Pagano, Angela; Rossi-Ashton, James A.; Donald, James R.; Epton, Ryan G.; Churchill, Jonathan C.; James, Michael J.; O'Brien, Peter; Taylor, Richard J. K.; Unsworth, William P. Visible-light-induced intramolecular charge transfer in the radical spirocyclisation of indole-tethered ynones Chemical Science, 2020, 11, 1353-1360 |
| 1556844 | CIF | C45 H57 B N2 O2 | P -1 | 9.6381; 11.485; 19.0369 85.238; 75.946; 75.838 | 1981.44 | Bhunia, Mrinal; Sahoo, Sumeet Ranjan; Das, Arpan; Ahmed, Jasimuddin; P., Sreejyothi; Mandal, Swadhin K. Transition metal-free catalytic reduction of primary amides using an abnormal NHC based potassium complex: integrating nucleophilicity with Lewis acidic activation Chemical Science, 2020, 11, 1848-1854 |
| 1556845 | CIF | C244 H327 Ag31 Cl5 F24 O2 P6 Pt S16 Sb4 | P -1 | 21.515; 24.1156; 35.321 81.037; 78.006; 68.595 | 16625 | Kang, Xi; Jin, Shan; Xiong, Lin; Wei, Xiao; Zhou, Manman; Qin, Chenwanli; Pei, Yong; Wang, Shuxin; Zhu, Manzhou Nanocluster growth <i>via</i> "graft-onto": effects on geometric structures and optical properties. Chemical science, 2020, 11, 1691-1697 |
| 1556846 | CIF | C11 H13 F9 O2 | P 21 21 21 | 5.6044; 9.5819; 26.472 90; 90; 90 | 1421.57 | Sperandio, Céline; Rodriguez, Jean; Quintard, Adrien Development of copper-catalyzed enantioselective decarboxylative aldolization for the preparation of perfluorinated 1,3,5-triols featuring supramolecular recognition properties. Chemical science, 2020, 11, 1629-1635 |
| 1556847 | CIF | C7 H10 F6 O3 | P 1 21 1 | 4.9029; 9.8824; 10.7838 90; 100.543; 90 | 513.68 | Sperandio, Céline; Rodriguez, Jean; Quintard, Adrien Development of copper-catalyzed enantioselective decarboxylative aldolization for the preparation of perfluorinated 1,3,5-triols featuring supramolecular recognition properties. Chemical science, 2020, 11, 1629-1635 |
| 1556860 | CIF | C45 H44 Cl F5 N4 Ni | P 1 21/c 1 | 19.2423; 10.9261; 21.5899 90; 106.046; 90 | 4362.3 | Dong, Yuyang; Lukens, James T.; Clarke, Ryan M.; Zheng, Shao-Liang; Lancaster, Kyle M.; Betley, Theodore A. Synthesis, characterization and C‒H amination reactivity of nickel iminyl complexes Chemical Science, 2020, 11, 1260-1268 |
| 1556861 | CIF | C45 H50 F5 N3 Ni | P 1 21/c 1 | 12.0799; 14.6404; 24.1769 90; 91.408; 90 | 4274.5 | Dong, Yuyang; Lukens, James T.; Clarke, Ryan M.; Zheng, Shao-Liang; Lancaster, Kyle M.; Betley, Theodore A. Synthesis, characterization and C‒H amination reactivity of nickel iminyl complexes Chemical Science, 2020, 11, 1260-1268 |
| 1556862 | CIF | C44 H45 F5 N3 Ni | P -1 | 9.5949; 11.8426; 18.3253 92.953; 104.293; 100.626 | 1972.9 | Dong, Yuyang; Lukens, James T.; Clarke, Ryan M.; Zheng, Shao-Liang; Lancaster, Kyle M.; Betley, Theodore A. Synthesis, characterization and C‒H amination reactivity of nickel iminyl complexes Chemical Science, 2020, 11, 1260-1268 |
| 1556863 | CIF | C45 H49 F5 N3 Ni | P n a 21 | 14.1294; 16.6197; 15.8282 90; 90; 90 | 3716.9 | Dong, Yuyang; Lukens, James T.; Clarke, Ryan M.; Zheng, Shao-Liang; Lancaster, Kyle M.; Betley, Theodore A. Synthesis, characterization and C‒H amination reactivity of nickel iminyl complexes Chemical Science, 2020, 11, 1260-1268 |
| 1556864 | CIF | C40 H39 F5 N3 Ni | P 1 21/c 1 | 17.7017; 15.1269; 13.141 90; 109.571; 90 | 3315.5 | Dong, Yuyang; Lukens, James T.; Clarke, Ryan M.; Zheng, Shao-Liang; Lancaster, Kyle M.; Betley, Theodore A. Synthesis, characterization and C‒H amination reactivity of nickel iminyl complexes Chemical Science, 2020, 11, 1260-1268 |
| 1556865 | CIF | C12 H8 I2 N2 O7 | P n a 21 | 8.2007; 7.7793; 24.6164 90; 90; 90 | 1570.42 | Zhang, Guangtao; Wang, Yuanxun; Xu, Jun; Sun, Jiyun; Sun, Fengxia; Zhang, Yilin; Zhang, Chenglin; Du, Yunfei A new hypervalent iodine(iii/v) oxidant and its application to the synthesis of 2H-azirines Chemical Science, 2020, 11, 947-953 |
| 1556866 | CIF | C36 H50 B2 | P -1 | 9.035; 12.0924; 14.7514 92.899; 103.022; 103.134 | 1520.32 | Su, Xiaojun; Baker, J. J.; Martin, Caleb D. Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis. Chemical science, 2020, 11, 126-131 |
| 1556867 | CIF | C32 H35 B O | P 1 21/c 1 | 10.6036; 17.5824; 17.446 90; 125.621; 90 | 2643.98 | Su, Xiaojun; Baker, J. J.; Martin, Caleb D. Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis. Chemical science, 2020, 11, 126-131 |
| 1556868 | CIF | C34 H31 B O | P b c a | 10.0358; 12.1076; 43.226 90; 90; 90 | 5252.4 | Su, Xiaojun; Baker, J. J.; Martin, Caleb D. Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis. Chemical science, 2020, 11, 126-131 |
| 1556869 | CIF | C61 H60 Cl2 N4 O2 Ru | P 1 21/c 1 | 11.5545; 17.3432; 25.028 90; 95.757; 90 | 4990.1 | Wang, Hai-Xu; Wan, Qingyun; Low, Kam-Hung; Zhou, Cong-Ying; Huang, Jie-Sheng; Zhang, Jun-Long; Che, Chi-Ming Stable group 8 metal porphyrin mono- and bis(dialkylcarbene) complexes: synthesis, characterization, and catalytic activity. Chemical science, 2020, 11, 2243-2259 |
| 1556870 | CIF | C64 H52 F4 N4 Os | P -1 | 11.0536; 11.1353; 11.8926 97.46; 108.927; 107.647 | 1276.53 | Wang, Hai-Xu; Wan, Qingyun; Low, Kam-Hung; Zhou, Cong-Ying; Huang, Jie-Sheng; Zhang, Jun-Long; Che, Chi-Ming Stable group 8 metal porphyrin mono- and bis(dialkylcarbene) complexes: synthesis, characterization, and catalytic activity. Chemical science, 2020, 11, 2243-2259 |
| 1556871 | CIF | C59 H27 F20 Fe N5 | P 1 | 10.5317; 14.347; 17.434 76.71; 80.147; 84.826 | 2522.3 | Wang, Hai-Xu; Wan, Qingyun; Low, Kam-Hung; Zhou, Cong-Ying; Huang, Jie-Sheng; Zhang, Jun-Long; Che, Chi-Ming Stable group 8 metal porphyrin mono- and bis(dialkylcarbene) complexes: synthesis, characterization, and catalytic activity. Chemical science, 2020, 11, 2243-2259 |
| 1556872 | CIF | C59 H50 Cl3 D Fe N4 | P -1 | 11.3588; 13.5043; 16.5422 85.786; 84.24; 70.986 | 2384.6 | Wang, Hai-Xu; Wan, Qingyun; Low, Kam-Hung; Zhou, Cong-Ying; Huang, Jie-Sheng; Zhang, Jun-Long; Che, Chi-Ming Stable group 8 metal porphyrin mono- and bis(dialkylcarbene) complexes: synthesis, characterization, and catalytic activity. Chemical science, 2020, 11, 2243-2259 |
| 1556873 | CIF | C65.5 H39.5 F20 N8 Ru | C 1 2/c 1 | 24.815; 20.891; 24.043 90; 100.174; 90 | 12268 | Wang, Hai-Xu; Wan, Qingyun; Low, Kam-Hung; Zhou, Cong-Ying; Huang, Jie-Sheng; Zhang, Jun-Long; Che, Chi-Ming Stable group 8 metal porphyrin mono- and bis(dialkylcarbene) complexes: synthesis, characterization, and catalytic activity. Chemical science, 2020, 11, 2243-2259 |
| 1556874 | CIF | C48 H54 Cu F12 N6 O2 P2 | P 1 21/n 1 | 21.313; 9.951; 24.687 90; 107.778; 90 | 4986 | Ryan, Michael C.; Kim, Yeon Jung; Gerken, James B.; Wang, Fei; Aristov, Michael M.; Martinelli, Joseph R.; Stahl, Shannon S. Mechanistic insights into copper-catalyzed aerobic oxidative coupling of N‒N bonds Chemical Science, 2020, 11, 1170-1175 |
| 1556875 | CIF | C311.2 H387.9 B90.2 F18 Fe4 N55.5 O36 S6 | C 1 c 1 | 33.357; 32.3478; 45.8124 90; 102.32; 90 | 48294.4 | Lu, Zhenpin; Ronson, Tanya K.; Nitschke, Jonathan R. Reversible reduction drives anion ejection and C60 binding within an FeII4L6 cage Chemical Science, 2020, 11, 1097-1101 |
| 1556876 | CIF | C26 H42 N2 S8 Sn2 | P -1 | 7.7711; 10.3961; 12.6341 113.062; 96.284; 98.114 | 914.39 | Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S. Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds Chemical Science, 2020, 11, 1066-1078 |
| 1556877 | CIF | C120 H88 B2 F48 Fe2 O2 S8 Sn2 | P 1 21/c 1 | 12.734; 31.568; 18.543 90; 107.358; 90 | 7115 | Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S. Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds Chemical Science, 2020, 11, 1066-1078 |
| 1556878 | CIF | C57 H53.5 B F24 N0.5 O0.5 S8 Sn2 | P 1 21/c 1 | 9.5804; 23.505; 30.294 90; 97.92; 90 | 6756.8 | Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S. Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds Chemical Science, 2020, 11, 1066-1078 |
| 1556879 | CIF | C122 H72 B2 F48 Ni2 P4 S8 | C 1 2/c 1 | 40.752; 18.985; 17.7197 90; 107.903; 90 | 13045.5 | Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S. Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds Chemical Science, 2020, 11, 1066-1078 |
| 1556880 | CIF | C90 H60 B F24 Ni2 P4 S8 | P -1 | 14.1624; 18.3974; 20.189 94.073; 103.397; 106.515 | 4852.9 | Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S. Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds Chemical Science, 2020, 11, 1066-1078 |
| 1556881 | CIF | C102 H92 B2 F48 O4 S8 Sn2 | P -1 | 12.9111; 15.863; 16.368 88.537; 88.979; 69.195 | 3132.6 | Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S. Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds Chemical Science, 2020, 11, 1066-1078 |
| 1556882 | CIF | C106 H68 B F24 Fe2 P4 Pd2 S8 | P -1 | 13.503; 19.054; 28.239 105.082; 91.975; 90.73 | 7009 | Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S. Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds Chemical Science, 2020, 11, 1066-1078 |
| 1556883 | CIF | C540 H360 B6 F144 P24 Pd12 S48 | P -1 | 29.421; 31.324; 35.123 92.011; 91.984; 99.304 | 31897 | Xie, Jiaze; Boyn, Jan-Niklas; Filatov, Alexander S.; McNeece, Andrew J.; Mazziotti, David A.; Anderson, John S. Redox, transmetalation, and stacking properties of tetrathiafulvalene-2,3,6,7-tetrathiolate bridged tin, nickel, and palladium compounds Chemical Science, 2020, 11, 1066-1078 |
| 1556884 | CIF | C40 H36 F6 N3 O3 P | P 1 21 1 | 8.20579; 29.4208; 16.5731 90; 93.223; 90 | 3994.76 | Duwald, Romain; Bosson, Johann; Pascal, Simon; Grass, Stéphane; Zinna, Francesco; Besnard, Céline; Di Bari, Lorenzo; Jacquemin, Denis; Lacour, Jérôme Merging polyacenes and cationic helicenes: from weak to intense chiroptical properties in the far red region Chemical Science, 2020, 11, 1165-1169 |
| 1556885 | CIF | C61 H46 F6 N5 O2 P | C 1 2/c 1 | 27.6234; 16.7146; 21.7661 90; 106.545; 90 | 9633.6 | Duwald, Romain; Bosson, Johann; Pascal, Simon; Grass, Stéphane; Zinna, Francesco; Besnard, Céline; Di Bari, Lorenzo; Jacquemin, Denis; Lacour, Jérôme Merging polyacenes and cationic helicenes: from weak to intense chiroptical properties in the far red region Chemical Science, 2020, 11, 1165-1169 |
| 1556886 | CIF | C95 H78 Cl6 F12 N6 O2 P2 | P 1 21/c 1 | 11.678; 12.9347; 27.785 90; 90.912; 90 | 4196.4 | Duwald, Romain; Bosson, Johann; Pascal, Simon; Grass, Stéphane; Zinna, Francesco; Besnard, Céline; Di Bari, Lorenzo; Jacquemin, Denis; Lacour, Jérôme Merging polyacenes and cationic helicenes: from weak to intense chiroptical properties in the far red region Chemical Science, 2020, 11, 1165-1169 |
| 1556900 | CIF | C62 H79 Cl2 N5 O6 Pt S | I 1 2/a 1 | 26.7934; 12.4321; 39.1414 90; 106.494; 90 | 12501.4 | Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M. Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour Chemical Science, 2020, 11, 1839-1847 |
| 1556901 | CIF | C67 H79 B2 F8 N7 O6 Pt | P -1 | 10.1982; 18.2063; 19.7708 105.665; 99.693; 96.105 | 3439.2 | Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M. Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour Chemical Science, 2020, 11, 1839-1847 |
| 1556902 | CIF | C65 H76 F6 N6 O6 Pt Sb | P -1 | 11.78747; 15.5279; 22.4447 101.252; 102.144; 103.723 | 3769.49 | Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M. Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour Chemical Science, 2020, 11, 1839-1847 |
| 1556903 | CIF | C66 H77 B F4 N8 O5 Pt | P 1 21/n 1 | 21.738; 14.9289; 21.8888 90; 107.531; 90 | 6773.5 | Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M. Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour Chemical Science, 2020, 11, 1839-1847 |
| 1556904 | CIF | C69 H85 Ag F12 N6 O6 Pt Sb2 | P 1 21/n 1 | 18.7462; 15.4022; 27.6759 90; 104.791; 90 | 7726.1 | Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M. Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour Chemical Science, 2020, 11, 1839-1847 |
| 1556905 | CIF | C60 H72 B F4 N5 O5 Pt | P -1 | 12.2375; 14.6363; 18.2789 81.118; 76.017; 74.098 | 3041.7 | Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M. Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour Chemical Science, 2020, 11, 1839-1847 |
| 1556906 | CIF | C67 H77 Ag F15 N7 O5 Pt Sb2.5 | P -1 | 13.0371; 18.3984; 18.4639 88.81; 89.789; 83.438 | 4398.8 | Zhang, Zhihui; Tizzard, Graham J.; Williams, J. A. Gareth; Goldup, Stephen M. Rotaxane PtII-complexes: mechanical bonding for chemically robust luminophores and stimuli responsive behaviour Chemical Science, 2020, 11, 1839-1847 |
| 1556907 | CIF | C23 H24 N2 O5 S | P 21 21 2 | 30.4605; 11.6596; 6.1159 90; 90; 90 | 2172.11 | Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality. Chemical science, 2020, 11, 1636-1642 |
| 1556908 | CIF | C20 H23 N3 O3 | P 21 21 21 | 7.191; 13.5045; 18.6644 90; 90; 90 | 1812.52 | Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality. Chemical science, 2020, 11, 1636-1642 |
| 1556909 | CIF | C20 H25 N3 O2 | P 1 21/n 1 | 6.8118; 17.5495; 15.1113 90; 91.427; 90 | 1805.9 | Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality. Chemical science, 2020, 11, 1636-1642 |
| 1556910 | CIF | C22 H21.25 N3 O2.125 | P 1 21 1 | 10.18405; 9.71457; 18.82762 90; 93.0169; 90 | 1860.1 | Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality. Chemical science, 2020, 11, 1636-1642 |
| 1556911 | CIF | C24 H21 F3 N2 O4 S | P 21 21 21 | 32.8358; 11.60538; 5.85758 90; 90; 90 | 2232.16 | Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality. Chemical science, 2020, 11, 1636-1642 |
| 1556912 | CIF | C22 H25 N3 O2 | P 1 21 1 | 12.4713; 9.02632; 17.84198 90; 92.8702; 90 | 2005.95 | Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality. Chemical science, 2020, 11, 1636-1642 |
| 1556913 | CIF | C20 H19 N3 O | P 1 21 1 | 10.10659; 5.94958; 13.62038 90; 99.5974; 90 | 807.53 | Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality. Chemical science, 2020, 11, 1636-1642 |
| 1556914 | CIF | C28 H30 N2 O2 | P 21 21 21 | 8.33247; 15.71709; 17.93381 90; 90; 90 | 2348.65 | Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality. Chemical science, 2020, 11, 1636-1642 |
| 1556915 | CIF | C24 H24 N2 O4 S | P 21 21 21 | 6.0985; 11.5023; 30.8387 90; 90; 90 | 2163.2 | Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality. Chemical science, 2020, 11, 1636-1642 |
| 1556992 | CIF | C18 H16 O4 | P b c n | 9.7263; 11.8883; 24.935 90; 90; 90 | 2883.2 | Liang, Kangjiang; Li, Tao; Li, Na; Zhang, Yang; Shen, Lei; Ma, Zhixian; Xia, Chengfeng Redox-neutral photochemical Heck-type arylation of vinylphenols activated by visible light Chemical Science, 2020, 11, 2130-2135 |
| 1556993 | CIF | C26 H24 N2 O2 S | P -1 | 10.6565; 11.1408; 12.3 69.374; 76.912; 65.303 | 1236.26 | Lee, Jiyoun; Ko, Donguk; Park, Hyunju; Yoo, Eun Jeong Direct cyclopropanation of activated N-heteroarenes <i>via</i> site- and stereoselective dearomative reactions. Chemical science, 2020, 11, 1672-1676 |
| 1556994 | CIF | C28 H26 N2 | P 21 21 21 | 9.072; 9.846; 23.918 90; 90; 90 | 2136.4 | Lee, Jiyoun; Ko, Donguk; Park, Hyunju; Yoo, Eun Jeong Direct cyclopropanation of activated N-heteroarenes <i>via</i> site- and stereoselective dearomative reactions. Chemical science, 2020, 11, 1672-1676 |
| 1556995 | CIF | C54 H31.2 F0.8 O8 Zn2 | C 1 2/c 1 | 37.1066; 31.0733; 11.8903 90; 99.208; 90 | 13533.1 | Lustig, William P.; Shen, Zeqing; Teat, Simon J.; Javed, Nasir; Velasco, Ever; O'Carroll, Deirdre M.; Li, Jing Rational design of a high-efficiency, multivariate metal‒organic framework phosphor for white LED bulbs Chemical Science, 2020, 11, 1814-1824 |
| 1557024 | CIF | C38 H34 S4 | C 1 2/c 1 | 41.708; 5.7563; 12.67 90; 98.46; 90 | 3008.8 | Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents Chemical Science, 2020, 11, 1825-1831 |
| 1557025 | CIF | C42 H42 S4 | P 1 21/c 1 | 23.82; 5.837; 12.5 90; 104.133; 90 | 1685 | Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents Chemical Science, 2020, 11, 1825-1831 |
| 1557026 | CIF | C42 H42 S4 | P 1 21/c 1 | 22.15; 5.7413; 13.1188 90; 95.85; 90 | 1659.6 | Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents Chemical Science, 2020, 11, 1825-1831 |
| 1557027 | CIF | C66 H30 Al3 Ba F89 O9 | P 1 c 1 | 28.173; 16.4313; 20.453 90; 90.107; 90 | 9468.1 | Schorpp, Marcel; Krossing, Ingo Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation. Chemical science, 2020, 11, 2068-2076 |
| 1557028 | CIF | C52 H26 Al2 Ca F68 O7 | P 1 21 1 | 17.765; 20.654; 20.031 90; 93.018; 90 | 7340 | Schorpp, Marcel; Krossing, Ingo Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation. Chemical science, 2020, 11, 2068-2076 |
| 1557029 | CIF | C36 H18 Al2 F55 In O6 | P -1 | 10.6319; 22.3961; 24.4869 79.144; 79.696; 77.759 | 5537.2 | Schorpp, Marcel; Krossing, Ingo Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation. Chemical science, 2020, 11, 2068-2076 |
| 1557030 | CIF | C50 H22 Al2 F74 Mg N6 O8 | P 1 | 14.3953; 18.2606; 25.8315 73.784; 74.37; 66.821 | 5895.1 | Schorpp, Marcel; Krossing, Ingo Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation. Chemical science, 2020, 11, 2068-2076 |
| 1557031 | CIF | C84 H34 Al4 F118 O12 Sr | P -1 | 13.8661; 20.2883; 23.0336 80.031; 85.985; 79.942 | 6278.6 | Schorpp, Marcel; Krossing, Ingo Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation. Chemical science, 2020, 11, 2068-2076 |
| 1557032 | CIF | C84 H34 Al4 Ca F118 O12 | P -1 | 13.9542; 20.3286; 22.9128 80.085; 84.743; 80.239 | 6296.8 | Schorpp, Marcel; Krossing, Ingo Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation. Chemical science, 2020, 11, 2068-2076 |
| 1557033 | CIF | C60 H26 Al3 Ca F87 O9 | P 1 21/c 1 | 23.429; 18.9075; 22.4874 90; 118.27; 90 | 8773.4 | Schorpp, Marcel; Krossing, Ingo Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation. Chemical science, 2020, 11, 2068-2076 |
| 1557034 | CIF | C66 H30 Al3 F89 O9 Sr | P -1 | 13.5412; 25.3825; 27.3385 90.017; 90.111; 92.474 | 9387.7 | Schorpp, Marcel; Krossing, Ingo Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation. Chemical science, 2020, 11, 2068-2076 |
| 1557045 | CIF | C17 H14 Cl N O2 | P 21 21 21 | 5.3182; 10.94; 23.9705 90; 90; 90 | 1394.63 | Burg, Finn; Breitenlechner, Stefan; Jandl, Christian; Bach, Thorsten Enantioselective oxygenation of exocyclic methylene groups by a manganese porphyrin catalyst with a chiral recognition site Chemical Science, 2020, 11, 2121-2129 |
| 1557052 | CIF | C22 H28 N | P -1 | 5.899; 7.547; 20.535 83.465; 84.681; 82.512 | 897.7 | Mongin, Cédric; Ardoy, Alejandro Mendez; Méreau, Raphaël; Bassani, Dario M.; Bibal, Brigitte Singlet oxygen stimulus for switchable functional organic cages Chemical Science, 2020, 11, 1478-1484 |
| 1557053 | CIF | C28 H18 O2 | P 1 21/c 1 | 13.0175; 9.329; 8.3512 90; 106.37; 90 | 973.06 | Mongin, Cédric; Ardoy, Alejandro Mendez; Méreau, Raphaël; Bassani, Dario M.; Bibal, Brigitte Singlet oxygen stimulus for switchable functional organic cages Chemical Science, 2020, 11, 1478-1484 |
| 1557060 | CIF | C18 H19 N S Si | P -1 | 8.52831; 10.39109; 11.21545 117.584; 92.3119; 95.1854 | 873.5 | Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B. From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes Chemical Science, 2020, 11, 1912-1917 |
| 1557061 | CIF | C17 H13 N O S | C 1 2/c 1 | 20.6204; 9.4103; 16.7239 90; 120.205; 90 | 2804.6 | Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B. From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes Chemical Science, 2020, 11, 1912-1917 |
| 1557062 | CIF | C18 H15 N O S | P b c a | 13.1964; 13.3812; 16.7048 90; 90; 90 | 2949.79 | Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B. From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes Chemical Science, 2020, 11, 1912-1917 |
| 1557063 | CIF | C11 H9 N O S | P 1 21/c 1 | 10.9143; 7.26579; 12.4737 90; 104.425; 90 | 957.99 | Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B. From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes Chemical Science, 2020, 11, 1912-1917 |
| 1557064 | CIF | C16 H21 N S Se Si | P 1 21/c 1 | 10.6588; 8.0663; 20.1272 90; 95.886; 90 | 1721.35 | Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B. From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes Chemical Science, 2020, 11, 1912-1917 |
| 1557065 | CIF | C22 H23 N S | P 1 21/c 1 | 13.9373; 7.7203; 17.0136 90; 105.984; 90 | 1759.89 | Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B. From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes Chemical Science, 2020, 11, 1912-1917 |
| 1557066 | CIF | C21 H20 S | P 1 21/n 1 | 7.5133; 25.6215; 8.2645 90; 100.591; 90 | 1563.83 | Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B. From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes Chemical Science, 2020, 11, 1912-1917 |
| 1557067 | CIF | C10 H7 N S | P -1 | 6.9027; 7.3743; 9.3503 68.861; 73.292; 84.246 | 425.18 | Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B. From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes Chemical Science, 2020, 11, 1912-1917 |
| 1557068 | CIF | C16 H11 N O S | P b c a | 12.2557; 9.5626; 21.5616 90; 90; 90 | 2526.94 | Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B. From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes Chemical Science, 2020, 11, 1912-1917 |
| 1557069 | CIF | C17 H17 N S | P 1 21/c 1 | 11.1885; 11.263; 12.1884 90; 116.756; 90 | 1371.48 | Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B. From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes Chemical Science, 2020, 11, 1912-1917 |
| 1557075 | CIF | C55 H67 N3 O6 P2 Ru | P 1 21/n 1 | 17.5623; 13.934; 20.8795 90; 92.113; 90 | 5106 | Artús Suàrez, Lluís; Jayarathne, Upul; Balcells, David; Bernskoetter, Wesley H.; Hazari, Nilay; Jaraiz, Martín; Nova, Ainara Rational selection of co-catalysts for the deaminative hydrogenation of amides. Chemical science, 2020, 11, 2225-2230 |
| 1557079 | CIF | C25 H23 N O3 | P 1 21 1 | 12.77764; 5.95718; 12.86001 90; 100.546; 90 | 962.352 | Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones Chemical Science, 2020, 11, 2401-2406 |
| 1557080 | CIF | C23 H29 N O2 | P 21 21 21 | 10.3193; 10.5258; 18.2046 90; 90; 90 | 1977.36 | Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones Chemical Science, 2020, 11, 2401-2406 |
| 1557081 | CIF | C25 H25 N O3 S | P 21 21 21 | 5.909; 12.8175; 27.4929 90; 90; 90 | 2082.27 | Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones Chemical Science, 2020, 11, 2401-2406 |
| 1557082 | CIF | C24 H18 O3 | C 1 2/c 1 | 21.613; 12.1859; 13.5922 90; 104.043; 90 | 3472.8 | He, Zhen; Perry, Gregory J. P.; Procter, David J. Sulfoxide-mediated oxidative cross-coupling of phenols Chemical Science, 2020, 11, 2001-2005 |
| 1557083 | CIF | C26 H24 O6 | P 1 21/c 1 | 14.145; 7.441; 24.56 90; 96.17; 90 | 2570 | He, Zhen; Perry, Gregory J. P.; Procter, David J. Sulfoxide-mediated oxidative cross-coupling of phenols Chemical Science, 2020, 11, 2001-2005 |
| 1557084 | CIF | C22 H15 Cl O3 | P 1 21/n 1 | 16.2589; 6.7715; 16.4568 90; 106.511; 90 | 1737.14 | He, Zhen; Perry, Gregory J. P.; Procter, David J. Sulfoxide-mediated oxidative cross-coupling of phenols Chemical Science, 2020, 11, 2001-2005 |
| 1557085 | CIF | C25 H24 O7 | P 1 21/n 1 | 12.5579; 5.2167; 35.021 90; 94.917; 90 | 2285.8 | He, Zhen; Perry, Gregory J. P.; Procter, David J. Sulfoxide-mediated oxidative cross-coupling of phenols Chemical Science, 2020, 11, 2001-2005 |
| 1557086 | CIF | C25 H28 O8 | C 1 2/c 1 | 29.9022; 11.0935; 13.4816 90; 99.73; 90 | 4407.8 | He, Zhen; Perry, Gregory J. P.; Procter, David J. Sulfoxide-mediated oxidative cross-coupling of phenols Chemical Science, 2020, 11, 2001-2005 |
| 1557087 | CIF | C39 H34 F6 N3 O P | P 1 21/c 1 | 9.3923; 29.4208; 11.9664 90; 102.511; 90 | 3228.14 | Zheng, Zheng; Liu, Haixiang; Zhai, Shaodong; Zhang, Haoke; Shan, Guogang; Kwok, Ryan T. K.; Ma, Chao; Sung, Herman H. Y.; Williams, Ian D.; Lam, Jacky W. Y.; Wong, Kam Sing; Hu, Xianglong; Tang, Ben Zhong Highly efficient singlet oxygen generation, two-photon photodynamic therapy and melanoma ablation by rationally designed mitochondria-specific near-infrared AIEgens Chemical Science, 2020, 11, 2494-2503 |
| 1557088 | CIF | C27 H22 N2 O | P 1 21/n 1 | 9.53897; 23.141; 9.5721 90; 107.33; 90 | 2017.04 | Zheng, Zheng; Liu, Haixiang; Zhai, Shaodong; Zhang, Haoke; Shan, Guogang; Kwok, Ryan T. K.; Ma, Chao; Sung, Herman H. Y.; Williams, Ian D.; Lam, Jacky W. Y.; Wong, Kam Sing; Hu, Xianglong; Tang, Ben Zhong Highly efficient singlet oxygen generation, two-photon photodynamic therapy and melanoma ablation by rationally designed mitochondria-specific near-infrared AIEgens Chemical Science, 2020, 11, 2494-2503 |
| 1557089 | CIF | C78 H190 Dy2 K2 N6 O21 Si12 | C 1 2/c 1 | 25.4899; 18.8304; 25.7453 90; 103.128; 90 | 12034.4 | Ryan, Austin J.; Ziller, Joseph W.; Evans, William J. The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions Chemical Science, 2020, 11, 2006-2014 |
| 1557090 | CIF | C42 H102 Dy K N3 O12 Si6 | P 1 21/n 1 | 11.0616; 27.199; 21.7721 90; 103.885; 90 | 6359 | Ryan, Austin J.; Ziller, Joseph W.; Evans, William J. The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions Chemical Science, 2020, 11, 2006-2014 |
| 1557091 | CIF | C78 H190 K2 N6 O21 Si12 Tm2 | C 1 2/c 1 | 25.453; 18.757; 25.744 90; 103.142; 90 | 11969 | Ryan, Austin J.; Ziller, Joseph W.; Evans, William J. The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions Chemical Science, 2020, 11, 2006-2014 |
| 1557092 | CIF | C42 H102 K N3 O12 Si6 Tm | P 21 21 21 | 21.956; 22.554; 25.737 90; 90; 90 | 12745 | Ryan, Austin J.; Ziller, Joseph W.; Evans, William J. The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions Chemical Science, 2020, 11, 2006-2014 |
| 1557093 | CIF | C52 H124 Gd2 K2 N4 O16 Si8 | P -1 | 12.6614; 15.5498; 21.205 94.4758; 94.0831; 105.746 | 3987.4 | Ryan, Austin J.; Ziller, Joseph W.; Evans, William J. The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions Chemical Science, 2020, 11, 2006-2014 |
| 1557094 | CIF | C36 H90 Gd K N5 O6 Si6 | R 3 2 :H | 18.564; 18.564; 18.05 90; 90; 120 | 5387 | Ryan, Austin J.; Ziller, Joseph W.; Evans, William J. The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions Chemical Science, 2020, 11, 2006-2014 |
| 1557095 | CIF | C42 H102 Er K N3 O12 Si6 | P 1 21/n 1 | 11.064; 27.08; 21.797 90; 103.991; 90 | 6337 | Ryan, Austin J.; Ziller, Joseph W.; Evans, William J. The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions Chemical Science, 2020, 11, 2006-2014 |
| 1557096 | CIF | C42 H102 Ho K N3 O12 Si6 | P 1 21/n 1 | 11.0476; 27.157; 21.797 90; 103.905; 90 | 6347.9 | Ryan, Austin J.; Ziller, Joseph W.; Evans, William J. The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions Chemical Science, 2020, 11, 2006-2014 |
| 1557097 | CIF | C42 H102 Gd K N3 O12 Si6 | P 1 21/n 1 | 11.1493; 27.059; 21.755 90; 104.007; 90 | 6368.1 | Ryan, Austin J.; Ziller, Joseph W.; Evans, William J. The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions Chemical Science, 2020, 11, 2006-2014 |
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