Crystallography Open Database
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Searching journal of publication like 'Chemical science' volume of publication is 13
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1565013 | CIF | C15 H20 Cl N O S | P 21 21 21 | 7.2165; 12.5371; 16.4763 90; 90; 90 | 1490.68 | Kremsmair, Alexander; Wilke, Henrik R.; Simon, Matthias M.; Schmidt, Quirin; Karaghiosoff, Konstantin; Knochel, Paul General stereoretentive preparation of chiral secondary mixed alkylmagnesium reagents and their use for enantioselective electrophilic aminations. Chemical science, 2021, 13, 44-49 |
| 1565226 | CIF | C10 H15 N O2 S | P 1 21 1 | 7.72; 7.7534; 9.0532 90; 94.725; 90 | 540.05 | Li, Peng-Fei; Ai, Yong; Zeng, Yu-Ling; Liu, Jun-Chao; Xu, Zhe-Kun; Wang, Zhong-Xia Highest-Tc single-component homochiral organic ferroelectrics Chemical Science, 2022, 13, 657-664 |
| 1565227 | CIF | C10 H15 N O2 S | P 1 21 1 | 7.7253; 7.7557; 9.0549 90; 94.727; 90 | 540.68 | Li, Peng-Fei; Ai, Yong; Zeng, Yu-Ling; Liu, Jun-Chao; Xu, Zhe-Kun; Wang, Zhong-Xia Highest-Tc single-component homochiral organic ferroelectrics Chemical Science, 2022, 13, 657-664 |
| 1565228 | CIF | C10 H15 N O2 S | P 1 21 1 | 7.748; 7.6312; 8.9986 90; 95.11; 90 | 529.941 | Li, Peng-Fei; Ai, Yong; Zeng, Yu-Ling; Liu, Jun-Chao; Xu, Zhe-Kun; Wang, Zhong-Xia Highest-Tc single-component homochiral organic ferroelectrics Chemical Science, 2022, 13, 657-664 |
| 1565229 | CIF | C10 H15 N O2 S | P 1 21/m 1 | 7.699; 7.6119; 8.9599 90; 94.873; 90 | 523.188 | Li, Peng-Fei; Ai, Yong; Zeng, Yu-Ling; Liu, Jun-Chao; Xu, Zhe-Kun; Wang, Zhong-Xia Highest-Tc single-component homochiral organic ferroelectrics Chemical Science, 2022, 13, 657-664 |
| 1565230 | CIF | C10 H15 N O2 S | P 1 21 1 | 7.7527; 7.6368; 8.9989 90; 95.097; 90 | 530.68 | Li, Peng-Fei; Ai, Yong; Zeng, Yu-Ling; Liu, Jun-Chao; Xu, Zhe-Kun; Wang, Zhong-Xia Highest-Tc single-component homochiral organic ferroelectrics Chemical Science, 2022, 13, 657-664 |
| 1565368 | CIF | C15 H9.97 Cl4.03 N2 S | P -1 | 7.3043; 9.0923; 12.6109 80.349; 86.679; 72.338 | 786.73 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565369 | CIF | C14 H8 Cl4 N2 O S | P -1 | 7.10603; 7.22142; 15.6955 83.2406; 78.4301; 71.106 | 745.33 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565370 | CIF | C15 H10 Cl4 N2 S | P 1 21/n 1 | 9.1703; 13.7683; 12.5807 90; 96.799; 90 | 1577.26 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565371 | CIF | C13 H6 Cl4 N2 S | P 1 21/n 1 | 14.4699; 13.6411; 16.045 90; 115.564; 90 | 2857 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565372 | CIF | C15 H10 Cl3 N2 S | P 1 21/n 1 | 11.5111; 7.7055; 16.9368 90; 104.127; 90 | 1456.8 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565373 | CIF | C14 H8 Cl4 N2 S | P -1 | 8.9856; 9.2182; 9.374 103.868; 94.53; 95.061 | 746.85 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565374 | CIF | C16 H12 Cl4 N2 O S | P -1 | 7.4264; 11.9574; 11.966 115.075; 91.228; 95.201 | 956.37 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565375 | CIF | C15 H9.88 Cl4.12 N2 S | P 1 21/n 1 | 7.8074; 15.8724; 13.5003 90; 105.795; 90 | 1609.82 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565376 | CIF | C15 H10 Cl4 N2 S | P 1 21/c 1 | 7.3899; 10.5325; 20.5855 90; 96.598; 90 | 1591.64 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565377 | CIF | C15 H10 Cl3 N2 S | P -1 | 9.9369; 12.2664; 13.3652 91.036; 107.068; 109.355 | 1457.25 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565378 | CIF | C16 H10.42 Cl5.58 N2 O S | P 1 21/n 1 | 6.5698; 16.562; 16.941 90; 93.51; 90 | 1839.9 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565379 | CIF | C13 H6 Cl7 Ga N2 S | P 1 21/c 1 | 9.5753; 9.8718; 20.099 90; 94.444; 90 | 1894.16 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565380 | CIF | C14 H8 Cl4 N2 O S | P -1 | 7.0073; 9.6628; 12.0172 95.257; 106.738; 101.231 | 754.78 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565381 | CIF | C14 H11 Cl6 N3 S | P -1 | 8.1354; 9.2414; 12.9459 90.608; 101.838; 105.699 | 914.81 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565382 | CIF | C12 H5.84 Cl2.16 N3 S | P 1 21/c 1 | 7.4291; 18.6148; 9.0438 90; 107.796; 90 | 1190.83 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565383 | CIF | C13.5 H7 Cl4 N2 S | P b c n | 16.7712; 13.1359; 13.0495 90; 90; 90 | 2874.87 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565384 | CIF | C14 H8 Cl4 N2 S | P 1 21 1 | 9.0246; 13.7857; 12.0756 90; 98.513; 90 | 1485.78 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565385 | CIF | C16 H12 Cl4 N2 S | P b c a | 14.2979; 14.0607; 16.3174 90; 90; 90 | 3280.43 | Borys, Andryj M.; Clark, Ewan R.; Saines, Paul J.; Alberola, Antonio; Rawson, Jeremy M. A short, versatile route towards benzothiadiazinyl radicals. Chemical science, 2021, 13, 149-158 |
| 1565407 | CIF | C20 H21 N | P n a 21 | 23.603; 6.0263; 10.4104 90; 90; 90 | 1480.8 | Chen, Jiahua; Lim, Jun Wei; Ong, Derek Yiren; Chiba, Shunsuke Iterative addition of carbon nucleophiles to <i>N</i>,<i>N</i>-dialkyl carboxamides for synthesis of α-tertiary amines. Chemical science, 2021, 13, 99-104 |
| 1565565 | CIF | C22 H17 F3 N2 O | P 1 21 1 | 9.4035; 10.6249; 9.5173 90; 95.379; 90 | 946.698 | Zhu, Wen-Run; Su, Qiong; Deng, Xiao-Yi; Liu, Jia-Sheng; Zhong, Tao; Meng, Shan-Shui; Yi, Ji-Tao; Weng, Jiang; Lu, Gui Organocatalytic enantioselective S<sub>N</sub>1-type dehydrative nucleophilic substitution: access to bis(indolyl)methanes bearing quaternary carbon stereocenters. Chemical science, 2021, 13, 170-177 |
| 1565566 | CIF | C27 H18 Br F3 N2 | P 21 21 21 | 10.1505; 19.0261; 11.5778 90; 90; 90 | 2235.96 | Zhu, Wen-Run; Su, Qiong; Deng, Xiao-Yi; Liu, Jia-Sheng; Zhong, Tao; Meng, Shan-Shui; Yi, Ji-Tao; Weng, Jiang; Lu, Gui Organocatalytic enantioselective S<sub>N</sub>1-type dehydrative nucleophilic substitution: access to bis(indolyl)methanes bearing quaternary carbon stereocenters. Chemical science, 2021, 13, 170-177 |
| 1565567 | CIF | C25 H22 F4 N2 O | P 21 21 21 | 10.311; 12.3464; 34.9989 90; 90; 90 | 4455.49 | Zhu, Wen-Run; Su, Qiong; Deng, Xiao-Yi; Liu, Jia-Sheng; Zhong, Tao; Meng, Shan-Shui; Yi, Ji-Tao; Weng, Jiang; Lu, Gui Organocatalytic enantioselective S<sub>N</sub>1-type dehydrative nucleophilic substitution: access to bis(indolyl)methanes bearing quaternary carbon stereocenters. Chemical science, 2021, 13, 170-177 |
| 1565568 | CIF | F4 I3 K3 O12 V2 | C m c 21 | 11.6074; 8.5215; 15.0981 90; 90; 90 | 1493.4 | Chen, Jin; Hu, Chun-Li; Lin, Yi-Lin; Chen, Yan; Chen, Qian-Qian; Mao, Jiang-Gao K3V2O3F4(IO3)3: a high-performance SHG crystal containing both five and six-coordinated V5+ cations Chemical Science, 2022, 13, 454-460 |
| 1565569 | CIF | C24 H36 B Cl3 N6 O2 W | P -1 | 10.2936; 11.0038; 13.3415 98.452; 102.852; 96.092 | 1442.14 | Timmermann, Christopher; Thiem, Paula; Wanitschke, Dominik; Hüttenschmidt, Mareike; Romischke, Johanna; Villinger, Alexander; Seidel, Wolfram W. Migratory insertion of isocyanide into a ketenyl-tungsten bond as key step in cyclization reactions. Chemical science, 2021, 13, 123-132 |
| 1565570 | CIF | C32.5 H43 B Cl3 N7 O4 W | P -1 | 9.9415; 11.0539; 17.5643 98.146; 97.68; 105.73 | 1808.92 | Timmermann, Christopher; Thiem, Paula; Wanitschke, Dominik; Hüttenschmidt, Mareike; Romischke, Johanna; Villinger, Alexander; Seidel, Wolfram W. Migratory insertion of isocyanide into a ketenyl-tungsten bond as key step in cyclization reactions. Chemical science, 2021, 13, 123-132 |
| 1565571 | CIF | C32.84 H43.68 B Cl1.68 N7 O4 W | P -1 | 10.2497; 11.3925; 16.0476 105.219; 96.074; 93.672 | 1789.8 | Timmermann, Christopher; Thiem, Paula; Wanitschke, Dominik; Hüttenschmidt, Mareike; Romischke, Johanna; Villinger, Alexander; Seidel, Wolfram W. Migratory insertion of isocyanide into a ketenyl-tungsten bond as key step in cyclization reactions. Chemical science, 2021, 13, 123-132 |
| 1565572 | CIF | C33.62 H45.25 B Cl1.25 N7 O4 W | P 1 21/c 1 | 9.8806; 22.4324; 17.6641 90; 105.658; 90 | 3769.9 | Timmermann, Christopher; Thiem, Paula; Wanitschke, Dominik; Hüttenschmidt, Mareike; Romischke, Johanna; Villinger, Alexander; Seidel, Wolfram W. Migratory insertion of isocyanide into a ketenyl-tungsten bond as key step in cyclization reactions. Chemical science, 2021, 13, 123-132 |
| 1565573 | CIF | C19 H23 B N6 O3 W | P -1 | 9.7834; 11.173; 11.3156 64.197; 72.129; 88.96 | 1050.19 | Timmermann, Christopher; Thiem, Paula; Wanitschke, Dominik; Hüttenschmidt, Mareike; Romischke, Johanna; Villinger, Alexander; Seidel, Wolfram W. Migratory insertion of isocyanide into a ketenyl-tungsten bond as key step in cyclization reactions. Chemical science, 2021, 13, 123-132 |
| 1565574 | CIF | C23 H32 B2 F4 N6 O3 W | P -1 | 10.3289; 11.4973; 13.0257 98.414; 113.051; 92.169 | 1400.32 | Timmermann, Christopher; Thiem, Paula; Wanitschke, Dominik; Hüttenschmidt, Mareike; Romischke, Johanna; Villinger, Alexander; Seidel, Wolfram W. Migratory insertion of isocyanide into a ketenyl-tungsten bond as key step in cyclization reactions. Chemical science, 2021, 13, 123-132 |
| 1565575 | CIF | C37 H53 B N8 O3 W | P 1 21/n 1 | 11.4957; 22.605; 14.7243 90; 99.238; 90 | 3776.6 | Timmermann, Christopher; Thiem, Paula; Wanitschke, Dominik; Hüttenschmidt, Mareike; Romischke, Johanna; Villinger, Alexander; Seidel, Wolfram W. Migratory insertion of isocyanide into a ketenyl-tungsten bond as key step in cyclization reactions. Chemical science, 2021, 13, 123-132 |
| 1565576 | CIF | C65 H84 B2 Cl6 N14 O7 W2 | P -1 | 15.3547; 15.392; 17.9913 82.881; 89.831; 62.331 | 3729.6 | Timmermann, Christopher; Thiem, Paula; Wanitschke, Dominik; Hüttenschmidt, Mareike; Romischke, Johanna; Villinger, Alexander; Seidel, Wolfram W. Migratory insertion of isocyanide into a ketenyl-tungsten bond as key step in cyclization reactions. Chemical science, 2021, 13, 123-132 |
| 1565577 | CIF | C30 H21 N3 O3 | P -1 | 9.6587; 11.5335; 12.4216 114.357; 102.222; 94.593 | 1210.05 | Lin, Wei; Zhao, Qun; Li, Yao; Pan, Ming; Yang, Chen; Yang, Guo-Hui; Li, Xin Asymmetric synthesis of N-N axially chiral compounds <i>via</i> organocatalytic atroposelective <i>N</i>-acylation. Chemical science, 2021, 13, 141-148 |
| 1565578 | CIF | C27 H20 N3 O P | P 1 21/c 1 | 8.7349; 18.3308; 14.1743 90; 94.763; 90 | 2261.72 | Duan, Chunbo; Xin, Ying; Wang, Zicheng; Zhang, Jing; Han, Chunmiao; Xu, Hui High-efficiency hyperfluorescent white light-emitting diodes based on high-concentration-doped TADF sensitizer matrices <i>via</i> spatial and energy gap effects. Chemical science, 2021, 13, 159-169 |
| 1565579 | CIF | C40 H28 Cl2 N5 O P | P 1 21/c 1 | 18.7793; 8.0735; 26.4549 90; 122.492; 90 | 3383.1 | Duan, Chunbo; Xin, Ying; Wang, Zicheng; Zhang, Jing; Han, Chunmiao; Xu, Hui High-efficiency hyperfluorescent white light-emitting diodes based on high-concentration-doped TADF sensitizer matrices <i>via</i> spatial and energy gap effects. Chemical science, 2021, 13, 159-169 |
| 1565580 | CIF | C33 H23 N4 O P | P b c a | 8.265; 23.677; 26.571 90; 90; 90 | 5200 | Duan, Chunbo; Xin, Ying; Wang, Zicheng; Zhang, Jing; Han, Chunmiao; Xu, Hui High-efficiency hyperfluorescent white light-emitting diodes based on high-concentration-doped TADF sensitizer matrices <i>via</i> spatial and energy gap effects. Chemical science, 2021, 13, 159-169 |
| 1565590 | CIF | C18 H15 Br Cl F2 N O2 | P 1 21 1 | 11.04668; 5.51936; 14.34857 90; 101.385; 90 | 857.627 | Xu, Xiao; Bao, Longzhu; Ran, Lu; Yang, Zhenyan; Yan, Dingce; Wang, Chun-Jiang; Teng, Huailong Synthesis of bioactive fluoropyrrolidines via copper(i)-catalysed asymmetric 1,3-dipolar cycloaddition of azomethine ylides Chemical Science, 2022, 13, 1398-1407 |
| 1565601 | CIF | C27 H29 N3 O4 | P 1 21/c 1 | 11.3563; 16.7472; 12.6545 90; 101.483; 90 | 2358.54 | Kuhn, Ariel J.; Ehlke, Beatriz; Johnstone, Timothy C.; Oliver, Scott R. J.; Raskatov, Jevgenij A. A crystal-structural study of Pauling–Corey rippled sheets Chemical Science, 2022, 13, 671-680 |
| 1565602 | CIF | C40 H52 O2 S2 Si2 | P -1 | 14.2639; 14.5005; 20.4969 105.307; 109.588; 90.479 | 3830.5 | Gao, Yunpeng; Feng, Chi; Seo, Tamae; Kubota, Koji; Ito, Hajime Efficient access to materials-oriented aromatic alkynes via the mechanochemical Sonogashira coupling of solid aryl halides with large polycyclic conjugated systems Chemical Science, 2022, 13, 430-438 |
| 1565603 | CIF | C42 H52 S5 Si2 | C 1 2/c 1 | 39.5034; 9.2352; 23.1512 90; 96.916; 90 | 8384.61 | Gao, Yunpeng; Feng, Chi; Seo, Tamae; Kubota, Koji; Ito, Hajime Efficient access to materials-oriented aromatic alkynes via the mechanochemical Sonogashira coupling of solid aryl halides with large polycyclic conjugated systems Chemical Science, 2022, 13, 430-438 |
| 1565604 | CIF | C18 H14 Br N O2 | P 1 21/c 1 | 8.8605; 21.1565; 7.8415 90; 93.025; 90 | 1467.9 | Yuan, Da-Fu; Wang, Zi-Chen; Geng, Rui-Sen; Ren, Guang-Yi; Wright, James S.; Ni, Shao-Fei; Li, Ming; Wen, Li-Rong; Zhang, Lin-Bao Hypervalent iodine promoted the synthesis of cycloheptatrienes and cyclopropanes Chemical Science, 2022, 13, 478-485 |
| 1565605 | CIF | C20 H16 Br N O2 | P 1 21/c 1 | 7.9559; 6.808; 30.863 90; 91.251; 90 | 1671.26 | Yuan, Da-Fu; Wang, Zi-Chen; Geng, Rui-Sen; Ren, Guang-Yi; Wright, James S.; Ni, Shao-Fei; Li, Ming; Wen, Li-Rong; Zhang, Lin-Bao Hypervalent iodine promoted the synthesis of cycloheptatrienes and cyclopropanes Chemical Science, 2022, 13, 478-485 |
| 1565606 | CIF | C19 H16 F3 N O2 | P -1 | 9.4212; 10.7629; 18.7421 94.939; 96.779; 110.576 | 1750.05 | Yuan, Da-Fu; Wang, Zi-Chen; Geng, Rui-Sen; Ren, Guang-Yi; Wright, James S.; Ni, Shao-Fei; Li, Ming; Wen, Li-Rong; Zhang, Lin-Bao Hypervalent iodine promoted the synthesis of cycloheptatrienes and cyclopropanes Chemical Science, 2022, 13, 478-485 |
| 1565661 | CIF | C13 H14 O4 S | P 1 21 1 | 8.6416; 6.2775; 10.9475 90; 96.634; 90 | 589.9 | Goetzke, F. Wieland; Sidera, Mireia; Fletcher, Stephen P. Catalytic asymmetric hydrometallation of cyclobutenes with salicylaldehydes. Chemical science, 2021, 13, 236-240 |
| 1565662 | CIF | C34 H68 B Ce O2 Si2 | P 1 21/c 1 | 7.4686; 26.405; 19.52 90; 97.925; 90 | 3812.7 | Münzfeld, Luca; Sun, Xiaofei; Schlittenhardt, Sören; Schoo, Christoph; Hauser, Adrian; Gillhuber, Sebastian; Weigend, Florian; Ruben, Mario; Roesky, Peter W. Introduction of plumbole to f-element chemistry Chemical Science, 2022, 13, 945-954 |
| 1565663 | CIF | C30 H60 B Er O Si2 | P n m a | 15.8956; 24.908; 8.4943 90; 90; 90 | 3363.1 | Münzfeld, Luca; Sun, Xiaofei; Schlittenhardt, Sören; Schoo, Christoph; Hauser, Adrian; Gillhuber, Sebastian; Weigend, Florian; Ruben, Mario; Roesky, Peter W. Introduction of plumbole to f-element chemistry Chemical Science, 2022, 13, 945-954 |
| 1565664 | CIF | C34 H68 B O2 Si2 Sm | P 1 21/c 1 | 7.5051; 26.3267; 19.4417 90; 98.004; 90 | 3804 | Münzfeld, Luca; Sun, Xiaofei; Schlittenhardt, Sören; Schoo, Christoph; Hauser, Adrian; Gillhuber, Sebastian; Weigend, Florian; Ruben, Mario; Roesky, Peter W. Introduction of plumbole to f-element chemistry Chemical Science, 2022, 13, 945-954 |
| 1565665 | CIF | C58 H96 Er Li O Pb Si4 | P 1 21 1 | 13.3164; 13.319; 16.7792 90; 97.425; 90 | 2951.02 | Münzfeld, Luca; Sun, Xiaofei; Schlittenhardt, Sören; Schoo, Christoph; Hauser, Adrian; Gillhuber, Sebastian; Weigend, Florian; Ruben, Mario; Roesky, Peter W. Introduction of plumbole to f-element chemistry Chemical Science, 2022, 13, 945-954 |
| 1565666 | CIF | C65 H104 Li O Pb Si4 Sm | P 1 21/n 1 | 13.5678; 13.7727; 35.796 90; 93.725; 90 | 6674.9 | Münzfeld, Luca; Sun, Xiaofei; Schlittenhardt, Sören; Schoo, Christoph; Hauser, Adrian; Gillhuber, Sebastian; Weigend, Florian; Ruben, Mario; Roesky, Peter W. Introduction of plumbole to f-element chemistry Chemical Science, 2022, 13, 945-954 |
| 1565667 | CIF | C70 H126.8 Er Li O4 Pb Si4 | P 1 21/n 1 | 22.0069; 16.3287; 22.8084 90; 113.88; 90 | 7494.4 | Münzfeld, Luca; Sun, Xiaofei; Schlittenhardt, Sören; Schoo, Christoph; Hauser, Adrian; Gillhuber, Sebastian; Weigend, Florian; Ruben, Mario; Roesky, Peter W. Introduction of plumbole to f-element chemistry Chemical Science, 2022, 13, 945-954 |
| 1565668 | CIF | C58 H96 Ce Li O Pb Si4 | P 1 21 1 | 13.4211; 13.6559; 16.7671 90; 97.576; 90 | 3046.2 | Münzfeld, Luca; Sun, Xiaofei; Schlittenhardt, Sören; Schoo, Christoph; Hauser, Adrian; Gillhuber, Sebastian; Weigend, Florian; Ruben, Mario; Roesky, Peter W. Introduction of plumbole to f-element chemistry Chemical Science, 2022, 13, 945-954 |
| 1565669 | CIF | C73.5 H124 Er Li O8 Pb Si4 | P -1 | 13.1318; 13.3996; 24.0543 90.114; 99.276; 109.783 | 3923.4 | Münzfeld, Luca; Sun, Xiaofei; Schlittenhardt, Sören; Schoo, Christoph; Hauser, Adrian; Gillhuber, Sebastian; Weigend, Florian; Ruben, Mario; Roesky, Peter W. Introduction of plumbole to f-element chemistry Chemical Science, 2022, 13, 945-954 |
| 1565670 | CIF | C58 H97 La Li O Pb Si4 | P 1 21 1 | 13.4752; 13.6204; 16.909 90; 99.42; 90 | 3061.59 | Münzfeld, Luca; Sun, Xiaofei; Schlittenhardt, Sören; Schoo, Christoph; Hauser, Adrian; Gillhuber, Sebastian; Weigend, Florian; Ruben, Mario; Roesky, Peter W. Introduction of plumbole to f-element chemistry Chemical Science, 2022, 13, 945-954 |
| 1565671 | CIF | C16 H25 Cl2 Fe N3 O12 | P 1 21 1 | 14.194; 10.712; 15.769 90; 102.51; 90 | 2340.7 | Lee, Yool; Oh, Chaeun; Kim, Jin; Park, Myong-Suk; Bae, Woo Kyun; Yoo, Kyung Hyun; Hong, Seungwoo Bioinspired nonheme iron complex that triggers mitochondrial apoptotic signalling pathway specifically for colorectal cancer cells Chemical Science, 2022, 13, 737-747 |
| 1565672 | CIF | C32 H46 Cl4 Fe2 N6 O23 | C 1 2/c 1 | 15.9079; 17.3412; 16.1343 90; 90.724; 90 | 4450.5 | Lee, Yool; Oh, Chaeun; Kim, Jin; Park, Myong-Suk; Bae, Woo Kyun; Yoo, Kyung Hyun; Hong, Seungwoo Bioinspired nonheme iron complex that triggers mitochondrial apoptotic signalling pathway specifically for colorectal cancer cells Chemical Science, 2022, 13, 737-747 |
| 1565673 | CIF | C16 H21 Cl2 Mn N3 O2 | P n a 21 | 14.289; 8.933; 28.022 90; 90; 90 | 3576.8 | Lee, Yool; Oh, Chaeun; Kim, Jin; Park, Myong-Suk; Bae, Woo Kyun; Yoo, Kyung Hyun; Hong, Seungwoo Bioinspired nonheme iron complex that triggers mitochondrial apoptotic signalling pathway specifically for colorectal cancer cells Chemical Science, 2022, 13, 737-747 |
| 1565674 | CIF | C20 H16 O3 | P 1 21/n 1 | 7.5343; 17.2112; 11.5465 90; 95.379; 90 | 1490.69 | Tian, Ya-Ming; Wang, Huaiju; Ritu, ?; König, Burkhard Photocatalytic synthesis of tetra-substituted furans promoted by carbon dioxide. Chemical science, 2021, 13, 241-246 |
| 1565715 | CIF | C31 H20 N2 | P 1 21/c 1 | 18.4424; 17.3145; 7.318 90; 93.009; 90 | 2333.6 | Shang, Qian; Tang, Haifang; Liu, Yongping; Yin, MingMing; Su, Lebin; Xie, Shimin; Liu, Lixin; Yang, Wen; Chen, Yi; Dong, Jianyu; Zhou, Yongbo; Yin, Shuang-Feng Cu(i) catalysis for selective condensation/bicycloaromatization of two different arylalkynes: direct and general construction of functionalized C-N axial biaryl compounds. Chemical science, 2021, 13, 263-273 |
| 1565762 | CIF | C18 H15 Al F28 O3 Si | P 1 21/n 1 | 9.757; 17.585; 17.518 90; 90.187; 90 | 3006 | Barthélemy, Antoine; Glootz, Kim; Scherer, Harald; Hanske, Annaleah; Krossing, Ingo Ga±catalyzed hydrosilylation? About the surprising system Ga+/HSiR3/olefin, proof of oxidation with subvalent Ga+ and silylium catalysis with perfluoroalkoxyaluminate anions Chemical Science, 2022, 13, 439-453 |
| 1565790 | CIF | C80 H76 K Nd O6 Si4 | P 1 21/c 1 | 15.07667; 18.20509; 36.5229 90; 94.8279; 90 | 9988.95 | Willauer, Aurélien R.; Douair, Iskander; Chauvin, Anne-Sophie; Fadaei-Tirani, Farzaneh; Bünzli, Jean-Claude G.; Maron, Laurent; Mazzanti, Marinella Structure, reactivity and luminescence studies of triphenylsiloxide complexes of tetravalent lanthanides Chemical Science, 2022, 13, 681-691 |
| 1565791 | CIF | C84 H84 O7 Si4 Tb | C 1 2/c 1 | 16.445; 23.0841; 21.7459 90; 95.923; 90 | 8211.1 | Willauer, Aurélien R.; Douair, Iskander; Chauvin, Anne-Sophie; Fadaei-Tirani, Farzaneh; Bünzli, Jean-Claude G.; Maron, Laurent; Mazzanti, Marinella Structure, reactivity and luminescence studies of triphenylsiloxide complexes of tetravalent lanthanides Chemical Science, 2022, 13, 681-691 |
| 1565792 | CIF | C92 H78 N O5 P Pr Si4 | P 1 21/c 1 | 14.39059; 21.1314; 28.0674 90; 91.3627; 90 | 8532.69 | Willauer, Aurélien R.; Douair, Iskander; Chauvin, Anne-Sophie; Fadaei-Tirani, Farzaneh; Bünzli, Jean-Claude G.; Maron, Laurent; Mazzanti, Marinella Structure, reactivity and luminescence studies of triphenylsiloxide complexes of tetravalent lanthanides Chemical Science, 2022, 13, 681-691 |
| 1565793 | CIF | C84 H84 Ce O7 Si4 | C 1 2/c 1 | 16.5246; 23.1693; 21.7608 90; 95.951; 90 | 8286.5 | Willauer, Aurélien R.; Douair, Iskander; Chauvin, Anne-Sophie; Fadaei-Tirani, Farzaneh; Bünzli, Jean-Claude G.; Maron, Laurent; Mazzanti, Marinella Structure, reactivity and luminescence studies of triphenylsiloxide complexes of tetravalent lanthanides Chemical Science, 2022, 13, 681-691 |
| 1565794 | CIF | C94 H92 Ce K O6 Si4 | P b c a | 15.5527; 26.7995; 38.849 90; 90; 90 | 16192.4 | Willauer, Aurélien R.; Douair, Iskander; Chauvin, Anne-Sophie; Fadaei-Tirani, Farzaneh; Bünzli, Jean-Claude G.; Maron, Laurent; Mazzanti, Marinella Structure, reactivity and luminescence studies of triphenylsiloxide complexes of tetravalent lanthanides Chemical Science, 2022, 13, 681-691 |
| 1565795 | CIF | C84 H84 Gd K O7 Si4 | P 1 21/n 1 | 13.4724; 28.4527; 22.4563 90; 100.959; 90 | 8451.1 | Willauer, Aurélien R.; Douair, Iskander; Chauvin, Anne-Sophie; Fadaei-Tirani, Farzaneh; Bünzli, Jean-Claude G.; Maron, Laurent; Mazzanti, Marinella Structure, reactivity and luminescence studies of triphenylsiloxide complexes of tetravalent lanthanides Chemical Science, 2022, 13, 681-691 |
| 1565796 | CIF | C111 H99 K2 Nd O5 Si5 | P 1 21/n 1 | 19.0352; 23.9418; 22.3713 90; 92.2121; 90 | 10187.8 | Willauer, Aurélien R.; Douair, Iskander; Chauvin, Anne-Sophie; Fadaei-Tirani, Farzaneh; Bünzli, Jean-Claude G.; Maron, Laurent; Mazzanti, Marinella Structure, reactivity and luminescence studies of triphenylsiloxide complexes of tetravalent lanthanides Chemical Science, 2022, 13, 681-691 |
| 1565814 | CIF | C77 H81.33 Cl4.17 Co2 N8 O1.67 | P -3 | 31.1312; 31.1312; 15.5307 90; 90; 120 | 13035.1 | Zhou, Weinan; Sarma, Tridib; Su, Yonghuan; Lei, Chuanhu; Sessler, Jonathan L. Kinetic trapping of a cobalt(ii) metallocage using a carbazole-containing expanded carbaporphyrinoid ligand Chemical Science, 2022, 13, 692-697 |
| 1565815 | CIF | C81 H92 Cl8 N8 O3 Zn2 | P 1 21/c 1 | 28.535; 13.861; 20.682 90; 101.36; 90 | 8020 | Zhou, Weinan; Sarma, Tridib; Su, Yonghuan; Lei, Chuanhu; Sessler, Jonathan L. Kinetic trapping of a cobalt(ii) metallocage using a carbazole-containing expanded carbaporphyrinoid ligand Chemical Science, 2022, 13, 692-697 |
| 1565816 | CIF | C77 H80 Cl4 Co2 N8 | P 1 21/c 1 | 28.3373; 14.5574; 20.3283 90; 100.895; 90 | 8234.6 | Zhou, Weinan; Sarma, Tridib; Su, Yonghuan; Lei, Chuanhu; Sessler, Jonathan L. Kinetic trapping of a cobalt(ii) metallocage using a carbazole-containing expanded carbaporphyrinoid ligand Chemical Science, 2022, 13, 692-697 |
| 1565817 | CIF | C152 H152 N16 Pd4 | P -1 | 11.694; 20.7153; 27.718 68.59; 89.019; 82.809 | 6199 | Zhou, Weinan; Sarma, Tridib; Su, Yonghuan; Lei, Chuanhu; Sessler, Jonathan L. Kinetic trapping of a cobalt(ii) metallocage using a carbazole-containing expanded carbaporphyrinoid ligand Chemical Science, 2022, 13, 692-697 |
| 1565818 | CIF | C16 H24 B F4 N | I b a 2 | 26.2135; 48.489; 7.7284 90; 90; 90 | 9823.3 | Liu, Ming-Shang; Du, Hai-Wu; Shu, Wei Metal-free allylic C–H nitrogenation, oxygenation, and carbonation of alkenes by thianthrenation Chemical Science, 2022, 13, 1003-1008 |
| 1565819 | CIF | C24 H24 O3 | P 1 21 1 | 6.0869; 17.6346; 17.8806 90; 92.23; 90 | 1917.85 | Liu, Ming-Shang; Du, Hai-Wu; Shu, Wei Metal-free allylic C–H nitrogenation, oxygenation, and carbonation of alkenes by thianthrenation Chemical Science, 2022, 13, 1003-1008 |
| 1565820 | CIF | C24 H20 F6 O6 S4 | P 1 21/n 1 | 9.1824; 17.1893; 16.2826 90; 99.542; 90 | 2534.5 | Liu, Ming-Shang; Du, Hai-Wu; Shu, Wei Metal-free allylic C–H nitrogenation, oxygenation, and carbonation of alkenes by thianthrenation Chemical Science, 2022, 13, 1003-1008 |
| 1565821 | CIF | C23 H20 I N O2 | P b c a | 14.3788; 7.5241; 35.493 90; 90; 90 | 3839.9 | Dishman, Sarah N.; Laconsay, Croix J.; Fettinger, James C.; Tantillo, Dean J.; Shaw, Jared T. Divergent stereochemical outcomes in the insertion of donor/donor carbenes into the C–H bonds of stereogenic centers Chemical Science, 2022, 13, 1030-1036 |
| 1565822 | CIF | C23 H20 I N O2 | P 1 | 8.7754; 8.8984; 12.8772 99.2233; 96.0361; 91.197 | 986.31 | Dishman, Sarah N.; Laconsay, Croix J.; Fettinger, James C.; Tantillo, Dean J.; Shaw, Jared T. Divergent stereochemical outcomes in the insertion of donor/donor carbenes into the C–H bonds of stereogenic centers Chemical Science, 2022, 13, 1030-1036 |
| 1565823 | CIF | C33 H27 N O3 | P 1 | 6.3151; 11.198; 17.7567 85.4422; 85.449; 86.8128 | 1246.24 | Dishman, Sarah N.; Laconsay, Croix J.; Fettinger, James C.; Tantillo, Dean J.; Shaw, Jared T. Divergent stereochemical outcomes in the insertion of donor/donor carbenes into the C–H bonds of stereogenic centers Chemical Science, 2022, 13, 1030-1036 |
| 1565833 | CIF | C10 H14 O4 | P 1 21 1 | 6.29835; 10.64131; 7.53892 90; 103.504; 90 | 491.31 | Ai, Yong; Li, Peng-Fei; Yang, Meng-Juan; Xu, Yu-Qiu; Li, Meng-Zhen; Xiong, Ren-Gen An organic plastic ferroelectric with high Curie point Chemical Science, 2022, 13, 748-753 |
| 1565834 | CIF | C10 H14 O4 | P 1 21 1 | 6.3879; 10.8484; 7.6137 90; 103.203; 90 | 513.67 | Ai, Yong; Li, Peng-Fei; Yang, Meng-Juan; Xu, Yu-Qiu; Li, Meng-Zhen; Xiong, Ren-Gen An organic plastic ferroelectric with high Curie point Chemical Science, 2022, 13, 748-753 |
| 1565835 | CIF | C10 H11 Fe N4 | I -4 3 m | 17.1728; 17.1728; 17.1728 90; 90; 90 | 5064.3 | López-Cabrelles, Javier; Miguel-Casañ, Eugenia; Esteve-Rochina, María; Andres-Garcia, Eduardo; Vitórica-Yrezábal, Iñigo J.; Calbo, Joaquín; Mínguez Espallargas, Guillermo Multivariate sodalite zeolitic imidazolate frameworks: a direct solvent-free synthesis Chemical Science, 2022, 13, 842-847 |
| 1565836 | CIF | C12 H14 Fe N4 | I -4 3 m | 17.317; 17.317; 17.317 90; 90; 90 | 5193 | López-Cabrelles, Javier; Miguel-Casañ, Eugenia; Esteve-Rochina, María; Andres-Garcia, Eduardo; Vitórica-Yrezábal, Iñigo J.; Calbo, Joaquín; Mínguez Espallargas, Guillermo Multivariate sodalite zeolitic imidazolate frameworks: a direct solvent-free synthesis Chemical Science, 2022, 13, 842-847 |
| 1565837 | CIF | C25 H20 O4 | P 61 | 17.6742; 17.6742; 11.6231 90; 90; 120 | 3144.36 | Lang, Jiawen; Wang, Siyuan; He, Changli; Liu, Xiaohua; Feng, Xiaoming Asymmetric synthesis of isochromanone derivatives via trapping carboxylic oxonium ylides and aldol cascade Chemical Science, 2022, 13, 1163-1168 |
| 1565838 | CIF | C25 H22 O4 | P 21 21 21 | 6.5263; 13.9032; 21.5712 90; 90; 90 | 1957.29 | Lang, Jiawen; Wang, Siyuan; He, Changli; Liu, Xiaohua; Feng, Xiaoming Asymmetric synthesis of isochromanone derivatives via trapping carboxylic oxonium ylides and aldol cascade Chemical Science, 2022, 13, 1163-1168 |
| 1565840 | CIF | C22 H19 Cl5 N2 Zn | P 1 21/c 1 | 23.376; 10.6352; 20.2506 90; 106.848; 90 | 4818.4 | Frye, Connor W.; Egger, Dominic T.; Kounalis, Errikos; Pearce, Adam J.; Cheng, Yukun; Tonks, Ian A. α-Diimine synthesis via titanium-mediated multicomponent diimination of alkynes with C-nitrosos Chemical Science, 2022, 13, 1469-1477 |
| 1565906 | CIF | C24 H29 N O3 | C 1 2/c 1 | 32.9756; 9.2126; 13.7861 90; 101.232; 90 | 4107.88 | Zhang, Bei-Bei; Peng, Shuo; Wang, Feiyi; Lu, Cuifen; Nie, Junqi; Chen, Zuxing; Yang, Guichun; Ma, Chao Borane-catalyzed cascade Friedel–Crafts alkylation/[1,5]-hydride transfer/Mannich cyclization to afford tetrahydroquinolines Chemical Science, 2022, 13, 775-780 |
| 1565907 | CIF | C27 H27 N O3 | C 1 c 1 | 5.7626; 21.7654; 36.032 90; 91.845; 90 | 4516.98 | Zhang, Bei-Bei; Peng, Shuo; Wang, Feiyi; Lu, Cuifen; Nie, Junqi; Chen, Zuxing; Yang, Guichun; Ma, Chao Borane-catalyzed cascade Friedel–Crafts alkylation/[1,5]-hydride transfer/Mannich cyclization to afford tetrahydroquinolines Chemical Science, 2022, 13, 775-780 |
| 1565908 | CIF | C23 H26 N2 O3 | P 1 21 1 | 9.4239; 10.0699; 11.235 90; 103.712; 90 | 1035.79 | Liang, Hui; Ji, Dong-Sheng; Xu, Guo-Qiang; Luo, Yong-Chun; Zheng, Haixue; Xu, Peng-Fei Metal-free, visible-light induced enantioselective three-component dicarbofunctionalization and oxytrifluoromethylation of enamines via chiral phosphoric acid catalysis Chemical Science, 2022, 13, 1088-1094 |
| 1565909 | CIF | C12 H9 Br F N3 O | P 1 21 1 | 8.0916; 6.0738; 12.9097 90; 105.671; 90 | 610.89 | Komatsuda, Masaaki; Suto, Ayane; Kondo, Hiroki; Takada, Hiroyuki; Kato, Kenta; Saito, Bunnai; Yamaguchi, Junichiro Ring-opening fluorination of bicyclic azaarenes Chemical Science, 2022, 13, 665-670 |
| 1565910 | CIF | C16 H13 N O3 | P 1 21/c 1 | 8.8242; 7.5306; 19.3128 90; 96.98; 90 | 1273.85 | Li, Long-Hai; Wei, Hao-Zhao; Wei, Yin; Shi, Min The Morita–Baylis–Hillman reaction for non-electron-deficient olefins enabled by photoredox catalysis Chemical Science, 2022, 13, 1478-1483 |
| 1565911 | CIF | C13 H15 N O4 | P 1 21/c 1 | 6.8237; 21.9249; 8.5663 90; 96.654; 90 | 1272.96 | Li, Long-Hai; Wei, Hao-Zhao; Wei, Yin; Shi, Min The Morita–Baylis–Hillman reaction for non-electron-deficient olefins enabled by photoredox catalysis Chemical Science, 2022, 13, 1478-1483 |
| 1565912 | CIF | C22 H23 N O2 | P 1 21/c 1 | 11.917; 7.3388; 20.1019 90; 92.932; 90 | 1755.74 | Li, Long-Hai; Wei, Hao-Zhao; Wei, Yin; Shi, Min The Morita–Baylis–Hillman reaction for non-electron-deficient olefins enabled by photoredox catalysis Chemical Science, 2022, 13, 1478-1483 |
| 1565913 | CIF | C20 H21 N O2 | P -1 | 6.9435; 11.9044; 21.0418 74.164; 85.968; 83.016 | 1659.59 | Li, Long-Hai; Wei, Hao-Zhao; Wei, Yin; Shi, Min The Morita–Baylis–Hillman reaction for non-electron-deficient olefins enabled by photoredox catalysis Chemical Science, 2022, 13, 1478-1483 |
| 1565914 | CIF | C108 H128 Cl4 N12 O26 | P 1 21/c 1 | 13.6939; 19.0018; 50.945 90; 90.412; 90 | 13256 | Chen, Qiong; Lei, Ye; Wu, Guangcheng; Li, Qing; Pan, Yuanjiang; Li, Hao Ultramacrocyclization in water via external templation Chemical Science, 2022, 13, 798-803 |
| 1565915 | CIF | C49 H57 Cl2 N6 O11.5 | P -1 | 10.312; 20.687; 26.395 74.272; 81.268; 78.693 | 5285.6 | Chen, Qiong; Lei, Ye; Wu, Guangcheng; Li, Qing; Pan, Yuanjiang; Li, Hao Ultramacrocyclization in water via external templation Chemical Science, 2022, 13, 798-803 |
| 1565916 | CIF | C50 H52 F12 N6 O7 P2 | P -1 | 9.22; 19.51; 20.82 62.99; 86.96; 78.01 | 3260 | Chen, Qiong; Lei, Ye; Wu, Guangcheng; Li, Qing; Pan, Yuanjiang; Li, Hao Ultramacrocyclization in water via external templation Chemical Science, 2022, 13, 798-803 |
| 1565917 | CIF | C102 H102 Cl2 N38 O25 | P -1 | 14.5032; 23.2785; 23.8851 107.441; 93.266; 104.627 | 7366.6 | Chen, Qiong; Lei, Ye; Wu, Guangcheng; Li, Qing; Pan, Yuanjiang; Li, Hao Ultramacrocyclization in water via external templation Chemical Science, 2022, 13, 798-803 |
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