Crystallography Open Database
Search results
Result: there are 688 entries in the selection
Switch to the old layout of the pageDownload all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)
Searching journal of publication like 'Chemical science' volume of publication is 11
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
1557098 | CIF | C42 H102 K N3 O12 Si6 Tb | P 1 21/n 1 | 11.1324; 27.081; 21.775 90; 103.924; 90 | 6371.8 | 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 |
1557099 | CIF | C78 H190 Gd2 K2 N6 O21 Si12 | C 1 2/c 1 | 25.507; 18.806; 25.726 90; 103.21; 90 | 12014 | 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 |
1557100 | CIF | C42 H102 K N3 O12 Si6 Y | P 1 21/n 1 | 11.0774; 27.0905; 21.7959 90; 104; 90 | 6346.5 | 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 |
1557101 | CIF | C78 H190 Ho2 K2 N6 O21 Si12 | C 1 2/c 1 | 25.514; 18.8; 25.712 90; 103.167; 90 | 12009 | 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 |
1557105 | CIF | C104 H96 B4 F16 N8 O4 Pd2 | I 1 2/a 1 | 28.36; 12.35285; 27.666 90; 94.6541; 90 | 9660.2 | Lewis, James E. M.; Tarzia, Andrew; White, Andrew J. P.; Jelfs, Kim E. Conformational control of Pd2L4 assemblies with unsymmetrical ligands Chemical Science, 2020, 11, 677-683 |
1557106 | CIF | C123 H119 B4 F16 N17 O9 Pd2 | C 1 2/c 1 | 23.2193; 15.8896; 38.7298 90; 112.281; 90 | 13222.3 | Lewis, James E. M.; Tarzia, Andrew; White, Andrew J. P.; Jelfs, Kim E. Conformational control of Pd2L4 assemblies with unsymmetrical ligands Chemical Science, 2020, 11, 677-683 |
1557107 | CIF | C16 H19 I N2 | P 1 21/c 1 | 6.29025; 7.62301; 32.0065 90; 90.1584; 90 | 1534.73 | Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells Chemical Science, 2020, 11, 661-670 |
1557108 | CIF | C64 H87 I3 N5 O2 | P -1 | 14.6729; 15.6807; 16.4518 85.945; 73.88; 62.636 | 3222.3 | Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells Chemical Science, 2020, 11, 661-670 |
1557109 | CIF | C17 H18 I N2 | P 21 21 21 | 6.9063; 7.9318; 30.157 90; 90; 90 | 1651.98 | Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells Chemical Science, 2020, 11, 661-670 |
1557110 | CIF | C73 H92 N5 O2 U | P -1 | 13.2857; 13.9411; 20.5686 103.573; 95.666; 116.252 | 3230.4 | Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye Intra- and intermolecular interception of a photochemically generated terminal uranium nitride Chemical Science, 2020, 11, 2381-2387 |
1557111 | CIF | C75 H88 N8 U | P -1 | 13.1219; 13.5561; 20.3099 78.109; 76.264; 68.201 | 3230.5 | Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye Intra- and intermolecular interception of a photochemically generated terminal uranium nitride Chemical Science, 2020, 11, 2381-2387 |
1557112 | CIF | C76 H99 N6 O P U | P 1 21/c 1 | 25.884; 13.889; 21.315 90; 110.09; 90 | 7197 | Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye Intra- and intermolecular interception of a photochemically generated terminal uranium nitride Chemical Science, 2020, 11, 2381-2387 |
1557113 | CIF | C75 H96 N6 U | P 1 21/n 1 | 14.7113; 12.979; 36.748 90; 94.521; 90 | 6994.8 | Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye Intra- and intermolecular interception of a photochemically generated terminal uranium nitride Chemical Science, 2020, 11, 2381-2387 |
1557114 | CIF | C82 H101 N7 O U | P -1 | 13.1812; 15.8571; 19.6743 110.71; 90.48; 105.002 | 3692.6 | Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye Intra- and intermolecular interception of a photochemically generated terminal uranium nitride Chemical Science, 2020, 11, 2381-2387 |
1557115 | CIF | C33 H26 O2 | P 21 21 21 | 11.3659; 11.9259; 17.9314 90; 90; 90 | 2430.58 | Liu, Xihong; Zhang, Jingying; Bai, Lutao; Wang, Linqing; Yang, Dongxu; Wang, Rui Catalytic asymmetric multiple dearomatizations of phenols enabled by a cascade 1,8-addition and Diels‒Alder reaction Chemical Science, 2020, 11, 671-676 |
1557116 | CIF | C64 H88 | P -1 | 14.635; 18.1373; 22.0161 79.631; 75.201; 74.12 | 5396.2 | Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B. A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes. Chemical science, 2020, 11, 2051-2057 |
1557117 | CIF | C61 H39 B F24 N7 Rh | P -1 | 12.9083; 14.2464; 20.148 74.898; 79.351; 89.459 | 3512.7 | Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B. A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes. Chemical science, 2020, 11, 2051-2057 |
1557118 | CIF | C67 H62 B F24 N5 Rh | P -1 | 11.7452; 16.7896; 18.5777 84.062; 73.668; 70.038 | 3304.3 | Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B. A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes. Chemical science, 2020, 11, 2051-2057 |
1557119 | CIF | C32 H16 F8 | P -1 | 10.7497; 11.175; 11.5688 96.962; 96.945; 116.711 | 1207.93 | Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B. A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes. Chemical science, 2020, 11, 2051-2057 |
1557120 | CIF | C60 H51 B Cl2 F24 N5 Rh | C 1 c 1 | 19.4406; 17.1714; 19.516 90; 103.079; 90 | 6345.86 | Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B. A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes. Chemical science, 2020, 11, 2051-2057 |
1557121 | CIF | C54 H37 B F24 N5 Rh | C 1 2/c 1 | 16.95902; 18.45666; 34.7576 90; 98.7133; 90 | 10753.8 | Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B. A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes. Chemical science, 2020, 11, 2051-2057 |
1557122 | CIF | C68 H45 B F25 N5 O Rh | P -1 | 13.01044; 20.05043; 26.99316 90.7652; 97.9088; 106.636 | 6672.31 | Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B. A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes. Chemical science, 2020, 11, 2051-2057 |
1557123 | CIF | C21 H20 O6 | P 21 21 21 | 8.6977; 9.9164; 20.6241 90; 90; 90 | 1778.83 | Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A. Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis Chemical Science, 2020, 11, 2175-2180 |
1557124 | CIF | C37 H32 Br2 O9 | P 1 21/c 1 | 15.4799; 12.7561; 17.7032 90; 110.471; 90 | 3275 | Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A. Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis Chemical Science, 2020, 11, 2175-2180 |
1557125 | CIF | C20 H20 O6 | P 1 21/c 1 | 11.1979; 12.5205; 24.904 90; 93.401; 90 | 3485.5 | Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A. Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis Chemical Science, 2020, 11, 2175-2180 |
1557126 | CIF | C18 H16 O5 | P 1 21 1 | 11.2987; 10.6941; 11.9582 90; 90.723; 90 | 1444.79 | Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A. Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis Chemical Science, 2020, 11, 2175-2180 |
1557127 | CIF | C18 H18 O7 | P 1 21/n 1 | 13.6526; 9.772; 24.8831 90; 101.015; 90 | 3258.6 | Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A. Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis Chemical Science, 2020, 11, 2175-2180 |
1557128 | CIF | C27 H29 N O8 | P 1 21 1 | 10.1038; 12.0566; 10.4153 90; 97.827; 90 | 1256.95 | Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A. Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis Chemical Science, 2020, 11, 2175-2180 |
1557129 | CIF | C17 H20 O6 | P 1 21 1 | 7.091; 16.2621; 13.2704 90; 92.494; 90 | 1528.82 | Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A. Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis Chemical Science, 2020, 11, 2175-2180 |
1557130 | CIF | C27 H29 N O8 | C 1 2 1 | 26.9187; 7.6682; 12.9814 90; 108.271; 90 | 2544.5 | Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A. Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis Chemical Science, 2020, 11, 2175-2180 |
1557131 | CIF | C6 H5 D N2 | P b c a | 6.0431; 13.3857; 14.3592 90; 90; 90 | 1161.53 | Yang, Huan; Zhang, Li; Zhou, Fei-Yu; Jiao, Lei An umpolung approach to the hydroboration of pyridines: a novel and efficient synthesis of N-H 1,4-dihydropyridines Chemical Science, 2020, 11, 742-747 |
1557132 | CIF | In8 Ir1.5 S5.25 | P 3 1 m | 13.9378; 13.9378; 8.2316 90; 90; 120 | 1384.9 | Khoury, Jason F.; He, Jiangang; Pfluger, Jonathan E.; Hadar, Ido; Balasubramanian, Mahalingam; Stoumpos, Constantinos C.; Zu, Rui; Gopalan, Venkatraman; Wolverton, Chris; Kanatzidis, Mercouri G. Ir6In32S21, a polar, metal-rich semiconducting subchalcogenide Chemical Science, 2020, 11, 870-878 |
1557142 | CIF | C18 H20 Cl N3 O Pd | P -1 | 7.5074; 11.2005; 11.2581 70.42; 78.131; 84.462 | 872.46 | Czyz, Milena L.; Weragoda, Geethika K.; Horngren, Tyra H.; Connell, Timothy U.; Gomez, Daniel; O'Hair, Richard A. J.; Polyzos, Anastasios Photoexcited Pd(ii) auxiliaries enable light-induced control in C(sp3)‒H bond functionalisation Chemical Science, 2020, 11, 2455-2463 |
1557165 | CIF | C100 H102 Au4 P2 Ru2 S8 | P 1 21/c 1 | 13.9904; 14.295; 48.384 90; 94.664; 90 | 9644.4 | Sun, Yongnan; Pei, Wei; Xie, Mingcai; Xu, Shun; Zhou, Si; Zhao, Jijun; Xiao, Kang; Zhu, Yan Excitonic Au4Ru2(PPh3)2(SC2H4Ph)8 cluster for light-driven dinitrogen fixation Chemical Science, 2020, 11, 2440-2447 |
1557189 | CIF | C22 H12 F6 N2 O3 | P 1 21/n 1 | 10.7749; 15.2475; 12.314 90; 108.515; 90 | 1918.4 | Malla, Javid Ahmad; Umesh, Rintu M.; Vijay, Amal; Mukherjee, Arnab; Lahiri, Mayurika; Talukdar, Pinaki Apoptosis-inducing activity of a fluorescent barrel-rosette M+/Cl− channel Chemical Science, 2020, 11, 2420-2428 |
1557197 | CIF | C58 H62 N6 O13 Zn2 | P 1 21/c 1 | 15.21; 16.731; 23.716 90; 104.529; 90 | 5842 | Fu, Guorui; He, Yani; Li, Wentao; Miao, Tiezheng; Lü, Xingqiang; He, Hongshan; Liu, Li; Wong, Wai-Yeung Efficient white polymer light-emitting diodes (WPLEDs) based on covalent-grafting of [Zn2(MP)3(OAc)] into PVK Chemical Science, 2020, 11, 2640-2646 |
1557206 | CIF | C20 H30 N2 O2 | P 1 21/c 1 | 11.012; 16.138; 11.225 90; 96.899; 90 | 1980 | Chen, Hang; Ye, Hebo; Hai, Yu; Zhang, Ling; You, Lei n →π* interactions as a versatile tool for controlling dynamic imine chemistry in both organic and aqueous media Chemical Science, 2020, 11, 2707-2715 |
1557207 | CIF | C19 H29 N3 O2 | I 1 2/a 1 | 17.03; 10.58; 22.26 90; 103.23; 90 | 3904 | Chen, Hang; Ye, Hebo; Hai, Yu; Zhang, Ling; You, Lei n →π* interactions as a versatile tool for controlling dynamic imine chemistry in both organic and aqueous media Chemical Science, 2020, 11, 2707-2715 |
1557228 | CIF | C101 H48 F40 N12 Ni O7 | P n a 21 | 27.571; 19.7599; 19.1951 90; 90; 90 | 10457.5 | Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion Chemical Science, 2020, 11, 2790-2795 |
1557229 | CIF | C89.5 H19 Cl Cu F40 N8 Ni O3 | C 1 2/c 1 | 47.886; 13.8742; 28.061 90; 119.602; 90 | 16210 | Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion Chemical Science, 2020, 11, 2790-2795 |
1557230 | CIF | C89 H22 F40 N8 O3 | P -1 | 11.6188; 14.403; 26.7956 82.937; 77.65; 70.954 | 4133.7 | Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion Chemical Science, 2020, 11, 2790-2795 |
1557231 | CIF | C97 H32 F40 N12 Ni O3 | P -1 | 14.057; 14.08; 24.646 92.257; 101.581; 108.23 | 4511.4 | Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion Chemical Science, 2020, 11, 2790-2795 |
1557232 | CIF | C89 H18 Cu F40 N8 Ni O3 | P -1 | 14.0363; 14.1385; 24.8547 91.904; 101.174; 107.743 | 4586.3 | Li, Chengjie; Zhang, Kai; Ishida, Masatoshi; Li, Qizhao; Shimomura, Keito; Baryshnikov, Glib; Li, Xin; Savage, Mathew; Wu, Xin-Yan; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu Tripyrrin-armed isosmaragdyrins: synthesis, heterodinuclear coordination, and protonation-triggered helical inversion Chemical Science, 2020, 11, 2790-2795 |
1557234 | CIF | C61 H90 Au2 Cl2 F12 N2 P2 Sb2 | P 1 21/n 1 | 10.4398; 18.5854; 16.9617 90; 94.354; 90 | 3281.5 | Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes Chemical Science, 2020, 11, 2750-2758 |
1557235 | CIF | C34 H50 Au Cl2 F6 N O P Sb | P 1 21/c 1 | 10.9121; 17.7644; 19.509 90; 104.904; 90 | 3654.5 | Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes Chemical Science, 2020, 11, 2750-2758 |
1557236 | CIF | C33 H48 Au Cl2 F6 N O2 P Sb | P 1 21 1 | 14.8546; 12.2517; 20.5946 90; 99.848; 90 | 3692.9 | Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes Chemical Science, 2020, 11, 2750-2758 |
1557237 | CIF | C21 H20 N4 O5 | P 1 21/c 1 | 15.4212; 13.4652; 9.4134 90; 102.515; 90 | 1908.2 | Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes Chemical Science, 2020, 11, 2750-2758 |
1557238 | CIF | C29 H36 Au B10 Cl2 F6 P2 Sb | P 1 n 1 | 10.0221; 13.3021; 14.7578 90; 95.633; 90 | 1957.94 | Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes Chemical Science, 2020, 11, 2750-2758 |
1557239 | CIF | C38 H47 Au F6 N2 O2 P Sb | P 1 21/c 1 | 10.7728; 11.143; 30.591 90; 98.974; 90 | 3627.2 | Navarro, Miquel; Toledo, Alberto; Mallet-Ladeira, Sonia; Sosa Carrizo, E. Daiann; Miqueu, Karinne; Bourissou, Didier Versatility and adaptative behaviour of the P^N chelating ligand MeDalphos within gold(i) π complexes Chemical Science, 2020, 11, 2750-2758 |
1557253 | CIF | C54 H99 Am Br3 O3 P3 | P c a 21 | 28.768; 11.456; 18.185 90; 90; 90 | 5993 | Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E. Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes Chemical Science, 2020, 11, 2770-2782 |
1557254 | CIF | C54 H99 Br3 Nd O3 P3 | P c a 21 | 28.7058; 11.4228; 18.1359 90; 90; 90 | 5946.8 | Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E. Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes Chemical Science, 2020, 11, 2770-2782 |
1557255 | CIF | C54 H99 Br3 Ce O3 P3 | P c a 21 | 28.92; 11.434; 18.209 90; 90; 90 | 6021.2 | Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E. Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes Chemical Science, 2020, 11, 2770-2782 |
1557256 | CIF | C54 H99 Br3 La O3 P3 | P c a 21 | 28.879; 11.4223; 18.2083 90; 90; 90 | 6006.3 | Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E. Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes Chemical Science, 2020, 11, 2770-2782 |
1557257 | CIF | C54 H99 Br3 O3 P3 Pr | P c a 21 | 28.7155; 11.4126; 18.1299 90; 90; 90 | 5941.5 | Windorff, Cory J.; Celis-Barros, Cristian; Sperling, Joseph M.; McKinnon, Noah C.; Albrecht-Schmitt, Thomas E. Probing a variation of the inverse-trans-influence in americium and lanthanide tribromide tris(tricyclohexylphosphine oxide) complexes Chemical Science, 2020, 11, 2770-2782 |
1557262 | CIF | C21 H21 F O2 | P 1 21 1 | 6.512; 15.336; 8.7541 90; 111.502; 90 | 813.41 | Groves, Alistair; Sun, Jinwei; Parke, Hal R. I.; Callingham, Michael; Argent, Stephen P.; Taylor, Laurence J.; Lam, Hon Wai Catalytic enantioselective arylative cyclizations of alkynyl 1,3-diketones by 1,4-rhodium(i) migration Chemical Science, 2020, 11, 2759-2764 |
1557263 | CIF | C22 H22 O2 | P 21 21 21 | 9.5439; 10.5734; 17.3218 90; 90; 90 | 1747.97 | Groves, Alistair; Sun, Jinwei; Parke, Hal R. I.; Callingham, Michael; Argent, Stephen P.; Taylor, Laurence J.; Lam, Hon Wai Catalytic enantioselective arylative cyclizations of alkynyl 1,3-diketones by 1,4-rhodium(i) migration Chemical Science, 2020, 11, 2759-2764 |
1557283 | CIF | C25 H30 N4 O3 | P -1 | 6.6601; 7.4588; 23.5097 94.931; 90.774; 105.499 | 1120.43 | Shi, Xiujuan; Yan, Neng; Niu, Guangle; Sung, Simon H. P.; Liu, Zhiyang; Liu, Junkai; Kwok, Ryan T. K.; Lam, Jacky W. Y.; Wang, Wen-Xiong; Sung, Herman H.-Y.; Williams, Ian D.; Tang, Ben Zhong In vivo monitoring of tissue regeneration using a ratiometric lysosomal AIE probe Chemical Science, 2020, 11, 3152-3163 |
1557284 | CIF | C60 H44 Mn4 N12 O52 Si W12 | C 1 2/c 1 | 24.8686; 23.1581; 17.7369 90; 98.907; 90 | 10091.7 | Du, Jing; Lang, Zhong-Ling; Ma, Yuan-Yuan; Tan, Hua-Qiao; Liu, Bai-Ling; Wang, Yong-Hui; Kang, Zhen-Hui; Li, Yang-Guang Polyoxometalate-based electron transfer modulation for efficient electrocatalytic carbon dioxide reduction Chemical Science, 2020, 11, 3007-3015 |
1557285 | CIF | C49 H39 Mn3 Mo12 N11 O49 P | P -1 | 13.034; 15.6737; 20.2719 79.875; 88.908; 87.011 | 4071.1 | Du, Jing; Lang, Zhong-Ling; Ma, Yuan-Yuan; Tan, Hua-Qiao; Liu, Bai-Ling; Wang, Yong-Hui; Kang, Zhen-Hui; Li, Yang-Guang Polyoxometalate-based electron transfer modulation for efficient electrocatalytic carbon dioxide reduction Chemical Science, 2020, 11, 3007-3015 |
1557286 | CIF | C49 H39 Mn3 N11 O49 P W12 | P -1 | 13.0328; 15.6142; 20.1424 79.88; 89.029; 86.775 | 4028.6 | Du, Jing; Lang, Zhong-Ling; Ma, Yuan-Yuan; Tan, Hua-Qiao; Liu, Bai-Ling; Wang, Yong-Hui; Kang, Zhen-Hui; Li, Yang-Guang Polyoxometalate-based electron transfer modulation for efficient electrocatalytic carbon dioxide reduction Chemical Science, 2020, 11, 3007-3015 |
1557287 | CIF | C25 H22 N2 O3 | P 1 21 1 | 9.0919; 9.9836; 11.7719 90; 95.822; 90 | 1063.02 | Zhang, Xiang; Li, Xiang; Li, Jun-Long; Wang, Qi-Wei; Zou, Wen-Lin; Liu, Yan-Qing; Jia, Zhi-Qiang; Peng, Fu; Han, Bo Regiodivergent construction of medium-sized heterocycles from vinylethylene carbonates and allylidenemalononitriles Chemical Science, 2020, 11, 2888-2894 |
1557288 | CIF | C25 H22 N2 O3 | P 1 21/n 1 | 9.6576; 13.2796; 17.3578 90; 99.745; 90 | 2194 | Zhang, Xiang; Li, Xiang; Li, Jun-Long; Wang, Qi-Wei; Zou, Wen-Lin; Liu, Yan-Qing; Jia, Zhi-Qiang; Peng, Fu; Han, Bo Regiodivergent construction of medium-sized heterocycles from vinylethylene carbonates and allylidenemalononitriles Chemical Science, 2020, 11, 2888-2894 |
1557289 | CIF | C25 H22 N2 O3 | P -1 | 7.8691; 9.8641; 13.184 87.285; 85.531; 74.852 | 984.41 | Zhang, Xiang; Li, Xiang; Li, Jun-Long; Wang, Qi-Wei; Zou, Wen-Lin; Liu, Yan-Qing; Jia, Zhi-Qiang; Peng, Fu; Han, Bo Regiodivergent construction of medium-sized heterocycles from vinylethylene carbonates and allylidenemalononitriles Chemical Science, 2020, 11, 2888-2894 |
1557290 | CIF | C2 H Cl N4 | P b c a | 11.2724; 6.279; 12.5272 90; 90; 90 | 886.67 | Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl 3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines Chemical Science, 2020, 11, 3042-3047 |
1557291 | CIF | C8 H6 N4 O | P 1 21/c 1 | 10.7358; 5.14454; 14.9437 90; 105.056; 90 | 797.02 | Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl 3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines Chemical Science, 2020, 11, 3042-3047 |
1557292 | CIF | C10 H7 N5 | F d d 2 | 38.7645; 11.93147; 7.70847 90; 90; 90 | 3565.3 | Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl 3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines Chemical Science, 2020, 11, 3042-3047 |
1557293 | CIF | C9 H9 N7 O2 S2 | C 1 2/c 1 | 17.7417; 6.22991; 23.2377 90; 93.9389; 90 | 2562.38 | Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl 3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines Chemical Science, 2020, 11, 3042-3047 |
1557294 | CIF | C2 H Br N4 | P b c a | 12.7468; 5.60166; 12.9507 90; 90; 90 | 924.72 | Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl 3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines Chemical Science, 2020, 11, 3042-3047 |
1557295 | CIF | C17 H21 N5 O5 | C 1 2 1 | 32.663; 5.161; 11.0162 90; 94.704; 90 | 1850.79 | Schnell, Simon D.; Hoff, Lukas V.; Panchagnula, Advaita; Wurzenberger, Maximilian H. H.; Klapötke, Thomas M.; Sieber, Simon; Linden, Anthony; Gademann, Karl 3-Bromotetrazine: labelling of macromolecules via monosubstituted bifunctional s-tetrazines Chemical Science, 2020, 11, 3042-3047 |
1557296 | CIF | C22 H39 Al Ge Si2 | P 1 21/n 1 | 9.6414; 13.3432; 19.6279 90; 95.4683; 90 | 2513.6 | Albers, Lena; Tholen, Patrik; Schmidtmann, Marc; Müller, Thomas A germaaluminocene Chemical Science, 2020, 11, 2982-2986 |
1557298 | CIF | C6 H12 O6 | P 21 21 21 | 7.7012; 7.7746; 12.6751 90; 90; 90 | 758.91 | Zhou, Qing; Yang, Tianjia; Zhong, Zihao; Kausar, Fahmeeda; Wang, Ziyi; Zhang, Yongming; Yuan, Wang Zhang A clustering-triggered emission strategy for tunable multicolor persistent phosphorescence Chemical Science, 2020, 11, 2926-2933 |
1557299 | CIF | C5 H12 O4 | I -4 | 6.0826; 6.0826; 8.792 90; 90; 90 | 325.29 | Zhou, Qing; Yang, Tianjia; Zhong, Zihao; Kausar, Fahmeeda; Wang, Ziyi; Zhang, Yongming; Yuan, Wang Zhang A clustering-triggered emission strategy for tunable multicolor persistent phosphorescence Chemical Science, 2020, 11, 2926-2933 |
1557300 | CIF | C5 H10 O5 | P 21 21 21 | 5.6107; 9.1858; 12.5998 90; 90; 90 | 649.38 | Zhou, Qing; Yang, Tianjia; Zhong, Zihao; Kausar, Fahmeeda; Wang, Ziyi; Zhang, Yongming; Yuan, Wang Zhang A clustering-triggered emission strategy for tunable multicolor persistent phosphorescence Chemical Science, 2020, 11, 2926-2933 |
1557301 | CIF | C6 H12 O6 | P 21 21 21 | 8.091; 9.212; 10.056 90; 90; 90 | 749.5 | Zhou, Qing; Yang, Tianjia; Zhong, Zihao; Kausar, Fahmeeda; Wang, Ziyi; Zhang, Yongming; Yuan, Wang Zhang A clustering-triggered emission strategy for tunable multicolor persistent phosphorescence Chemical Science, 2020, 11, 2926-2933 |
1557331 | CIF | C203.82 H244.63 Cl7.63 N0 O40 | P -1 | 11.5721; 16.6408; 26.1539 84.725; 81.758; 89.936 | 4962.9 | Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P. Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes. Chemical science, 2020, 11, 2614-2620 |
1557332 | CIF | C112.95 H130.95 Cl15.56 O28 | P 1 | 14.334; 15.534; 16.891 69.752; 70.947; 76.995 | 3308.6 | Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P. Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes. Chemical science, 2020, 11, 2614-2620 |
1557333 | CIF | C106 H124 Cl6 O20 | P 1 21/n 1 | 19.6983; 20.2034; 26.3162 90; 97.77; 90 | 10377 | Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P. Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes. Chemical science, 2020, 11, 2614-2620 |
1557334 | CIF | C108.36 H122.64 Cl2.26 O20 | P 1 21/c 1 | 21.532; 19.643; 25.299 90; 90.699; 90 | 10699 | Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P. Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes. Chemical science, 2020, 11, 2614-2620 |
1557335 | CIF | C116.82 H140.82 Cl8.45 O28 | P -1 | 14.4911; 17.0462; 27.359 72.867; 86.978; 77.872 | 6313.8 | Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P. Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes. Chemical science, 2020, 11, 2614-2620 |
1557336 | CIF | C76 H74 O11 | P -1 | 13.0381; 16.6752; 17.4483 61.711; 79.037; 74.295 | 3207.14 | Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P. Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes. Chemical science, 2020, 11, 2614-2620 |
1557337 | CIF | C226.36 H257.54 O43.98 | P 1 21/c 1 | 21.154; 19.669; 25.429 90; 90.27; 90 | 10580 | Payne, Daniel T.; Webre, Whitney A.; Gobeze, Habtom B.; Seetharaman, Sairaman; Matsushita, Yoshitaka; Karr, Paul A.; Chahal, Mandeep K.; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S.; Ariga, Katsuhiko; D'Souza, Francis; Hill, Jonathan P. Nanomolecular singlet oxygen photosensitizers based on hemiquinonoid-resorcinarenes, the fuchsonarenes. Chemical science, 2020, 11, 2614-2620 |
1557338 | CIF | C31 H53 B Eu N5 O17 | P 1 21/n 1 | 13.2696; 15.8873; 18.2435 90; 93.3; 90 | 3839.7 | Breen, Colum; Pal, Robert; Elsegood, Mark R. J.; Teat, Simon J.; Iza, Felipe; Wende, Kristian; Buckley, Benjamin R.; Butler, Stephen J. Time-resolved luminescence detection of peroxynitrite using a reactivity-based lanthanide probe Chemical Science, 2020, 11, 3164-3170 |
1557341 | CIF | C15 H21 Cl0 N O2 | P 21 21 21 | 8.5161; 10.575; 15.9557 90; 90; 90 | 1436.93 | Lin, Qianchi; Hu, Bowen; Xu, Xi; Dong, Shunxi; Liu, Xiaohua; Feng, Xiaoming Chiral N,N′-dioxide/Mg(OTf)2 complex-catalyzed asymmetric [2,3]-rearrangement of in situ generated ammonium salts Chemical Science, 2020, 11, 3068-3073 |
1557360 | CIF | C8 H14 N2 O4 | P 1 21/c 1 | 5.6483; 9.0345; 9.1851 90; 103.599; 90 | 455.57 | Blake, Timothy R.; Ho, Wilson C.; Turlington, Christopher R.; Zang, Xiaoyu; Huttner, Melanie A.; Wender, Paul A.; Waymouth, Robert M. Synthesis and mechanistic investigations of pH-responsive cationic poly(aminoester)s Chemical Science, 2020, 11, 2951-2966 |
1557371 | CIF | C27 H19 N O3 | P 1 | 7.1378; 9.8466; 14.7942 88.9786; 79.0044; 74.6213 | 983.56 | Sasaki, Yui; Kojima, Soya; Hamedpour, Vahid; Kubota, Riku; Takizawa, Shin-ya; Yoshikawa, Isao; Houjou, Hirohiko; Kubo, Yuji; Minami, Tsuyoshi Accurate chiral pattern recognition for amines from just a single chemosensor Chemical Science, 2020, 11, 3790-3796 |
1557372 | CIF | C20 H12 S | P b c n | 21.4461; 8.4399; 7.3436 90; 90; 90 | 1329.21 | Xu, Niansheng; Zheng, Aibin; Wei, Yuefang; Yuan, Yi; Zhang, Jing; Lei, Ming; Wang, Peng D‒π‒D molecular semiconductors for perovskite solar cells: the superior role of helical versus planar π-linkers Chemical Science, 2020, 11, 3418-3426 |
1557373 | CIF | C48 H36 N2 O4 S | P -1 | 9.2973; 11.5371; 17.8524 99.629; 101.049; 97.562 | 1826.25 | Xu, Niansheng; Zheng, Aibin; Wei, Yuefang; Yuan, Yi; Zhang, Jing; Lei, Ming; Wang, Peng D‒π‒D molecular semiconductors for perovskite solar cells: the superior role of helical versus planar π-linkers Chemical Science, 2020, 11, 3418-3426 |
1557374 | CIF | C97 H78 Cl2 N4 O8 S2 | P -1 | 10.5796; 13.7266; 14.368 85.956; 83.941; 82.064 | 2051.7 | Xu, Niansheng; Zheng, Aibin; Wei, Yuefang; Yuan, Yi; Zhang, Jing; Lei, Ming; Wang, Peng D‒π‒D molecular semiconductors for perovskite solar cells: the superior role of helical versus planar π-linkers Chemical Science, 2020, 11, 3418-3426 |
1557376 | CIF | C22 H14 Au2 Fe N6 | P 1 21/c 1 | 10.8116; 14.4381; 14.9803 90; 96.596; 90 | 2322.93 | Chen, Yan-Cong; Meng, Yan; Dong, Yan-Jie; Song, Xiao-Wei; Huang, Guo-Zhang; Zhang, Chuan-Lei; Ni, Zhao-Ping; Navařík, Jakub; Malina, Ondřej; Zbořil, Radek; Tong, Ming-Liang Light- and temperature-assisted spin state annealing: accessing the hidden multistability Chemical Science, 2020, 11, 3281-3289 |
1557377 | CIF | C22 H14 Au2 Fe N6 | P 1 21/c 1 | 10.7397; 14.1109; 14.679 90; 95.98; 90 | 2212.5 | Chen, Yan-Cong; Meng, Yan; Dong, Yan-Jie; Song, Xiao-Wei; Huang, Guo-Zhang; Zhang, Chuan-Lei; Ni, Zhao-Ping; Navařík, Jakub; Malina, Ondřej; Zbořil, Radek; Tong, Ming-Liang Light- and temperature-assisted spin state annealing: accessing the hidden multistability Chemical Science, 2020, 11, 3281-3289 |
1557378 | CIF | C22 H14 Au2 Fe N6 | P 1 21/c 1 | 10.7739; 13.9861; 14.5762 90; 95.77; 90 | 2185.28 | Chen, Yan-Cong; Meng, Yan; Dong, Yan-Jie; Song, Xiao-Wei; Huang, Guo-Zhang; Zhang, Chuan-Lei; Ni, Zhao-Ping; Navařík, Jakub; Malina, Ondřej; Zbořil, Radek; Tong, Ming-Liang Light- and temperature-assisted spin state annealing: accessing the hidden multistability Chemical Science, 2020, 11, 3281-3289 |
1557379 | CIF | C22 H14 Au2 Fe N6 | P -1 | 10.7701; 14.1621; 14.7425 90.082; 96.077; 90.471 | 2235.9 | Chen, Yan-Cong; Meng, Yan; Dong, Yan-Jie; Song, Xiao-Wei; Huang, Guo-Zhang; Zhang, Chuan-Lei; Ni, Zhao-Ping; Navařík, Jakub; Malina, Ondřej; Zbořil, Radek; Tong, Ming-Liang Light- and temperature-assisted spin state annealing: accessing the hidden multistability Chemical Science, 2020, 11, 3281-3289 |
1557380 | CIF | C60 H56 B2 F8 N2 O8 | P 1 n 1 | 12.5252; 16.8071; 12.9207 90; 90.786; 90 | 2719.7 | Kim, Inwon; Im, Honggu; Lee, Hyeonyeong; Hong, Sungwoo N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts Chemical Science, 2020, 11, 3192-3197 |
1557381 | CIF | C23 H23 N O2 | P 1 21/c 1 | 9.3351; 20.6304; 9.7275 90; 105.289; 90 | 1807.1 | Kim, Inwon; Im, Honggu; Lee, Hyeonyeong; Hong, Sungwoo N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts Chemical Science, 2020, 11, 3192-3197 |
1557382 | CIF | C33 H28 B F4 N O2 | P 1 21/n 1 | 11.0604; 16.678; 15.1704 90; 100.639; 90 | 2750.3 | Kim, Inwon; Im, Honggu; Lee, Hyeonyeong; Hong, Sungwoo N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts Chemical Science, 2020, 11, 3192-3197 |
1557383 | CIF | C20 H21 N O4 | P 1 21/c 1 | 9.2314; 19.6394; 19.9121 90; 93.605; 90 | 3602.9 | Kim, Inwon; Im, Honggu; Lee, Hyeonyeong; Hong, Sungwoo N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts Chemical Science, 2020, 11, 3192-3197 |
1557384 | CIF | C17 H18 F2 O2 S | P 1 21/c 1 | 8.497; 13.357; 13.775 90; 85.689; 90 | 1559 | Huang, Xin; Zhang, Yage; Liang, Weijian; Zhang, Qifeng; Zhan, Yaling; Kong, Lichun; Peng, Bo Dearomatization of aryl sulfoxides: a switch between mono- and dual-difluoroalkylation Chemical Science, 2020, 11, 3048-3053 |
1557385 | CIF | C33 H29 Cl F4 O4 S2 | P -1 | 10.2309; 13.2445; 13.5012 66.799; 70.33; 75.627 | 1569.19 | Huang, Xin; Zhang, Yage; Liang, Weijian; Zhang, Qifeng; Zhan, Yaling; Kong, Lichun; Peng, Bo Dearomatization of aryl sulfoxides: a switch between mono- and dual-difluoroalkylation Chemical Science, 2020, 11, 3048-3053 |
1557394 | CIF | C16 H14 O2 | P 1 21 1 | 6.2309; 7.4169; 13.0054 90; 90.1686; 90 | 601.03 | Liu, Lei; Lee, Wes; Yuan, Mingbin; Acha, Chris; Geherty, Michael B.; Williams, Brandon; Gutierrez, Osvaldo Intra- and intermolecular Fe-catalyzed dicarbofunctionalization of vinyl cyclopropanes Chemical Science, 2020, 11, 3146-3151 |
1557395 | CIF | C102 H68 N18 O27 Zn8 | R -3 :H | 22.979; 22.979; 15.496 90; 90; 120 | 7086 | Chen, Sheng-Chun; Zhang, Fei-Hang; Huang, Kun-Lin; Tian, Feng; Zhang, Zhi-Hui; Zhou, Renxian; Feng, Xue-Jun; Zhou, Xiaoying; He, Ming-Yang; Gu, Jiande; Chen, Qun; Wu, Chuan-De The crucial roles of guest water in a biocompatible coordination network in the catalytic ring-opening polymerization of cyclic esters: a new mechanistic perspective Chemical Science, 2020, 11, 3345-3354 |
1557396 | CIF | C30 H26 B Br | P 1 21/c 1 | 16.2062; 8.1904; 17.137 90; 91.218; 90 | 2274.2 | Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J. The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies Chemical Science, 2020, 11, 3258-3267 |
1557397 | CIF | C36 H36 B Br | P -1 | 8.4803; 9.1672; 19.9099 80.254; 85.195; 68.593 | 1419.82 | Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J. The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies Chemical Science, 2020, 11, 3258-3267 |
1557398 | CIF | C22 H26 B Br O2 | P 1 21/n 1 | 6.4265; 15.8695; 20.617 90; 97.511; 90 | 2084.6 | Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J. The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies Chemical Science, 2020, 11, 3258-3267 |
1557399 | CIF | C62 H78 B2 Br2 | P -1 | 9.4752; 9.8107; 15.1088 93.579; 100.145; 90.47 | 1379.57 | Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J. The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies Chemical Science, 2020, 11, 3258-3267 |
1557400 | CIF | C22 H26 B Br O2 | P c a 21 | 20.7096; 6.4384; 15.5735 90; 90; 90 | 2076.52 | Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J. The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies Chemical Science, 2020, 11, 3258-3267 |
1557401 | CIF | C14 H10 B Br3 | P 1 21/n 1 | 13.2781; 5.936; 18.4485 90; 100.58; 90 | 1429.37 | Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J. The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies Chemical Science, 2020, 11, 3258-3267 |
1557402 | CIF | C44 H42 B2 Br2 O2 | P c c n | 42.071; 29.3977; 6.6541 90; 90; 90 | 8229.7 | Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J. The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies Chemical Science, 2020, 11, 3258-3267 |
1557403 | CIF | C28 H22 B Br O | P 1 21/c 1 | 16.0697; 19.1015; 7.184 90; 99.697; 90 | 2173.7 | Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J. The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies Chemical Science, 2020, 11, 3258-3267 |
1557404 | CIF | C100 H108 B4 Br4 | P -1 | 8.0182; 16.5443; 17.4491 64.933; 86.117; 77.027 | 2042.2 | Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J. The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies Chemical Science, 2020, 11, 3258-3267 |
1557405 | CIF | C62 H56 B2 Br2 | P -1 | 9.836; 10.894; 14.514 82.02; 73.02; 71.06 | 1405.2 | Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J. The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies Chemical Science, 2020, 11, 3258-3267 |
1557406 | CIF | C64 H68 B2 Br2 | P -1 | 13.45; 14.624; 15.214 91.36; 92.15; 116.43 | 2675.1 | Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J. The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies Chemical Science, 2020, 11, 3258-3267 |
1557428 | CIF | C33 H27 N2 O2 P | P -1 | 10.6898; 11.775; 11.9913 71.708; 65.4407; 89.239 | 1291.4 | Zhuang, Zeyan; Dai, Jun; Yu, Maoxing; Li, Jianqing; Shen, Pingchuan; Hu, Rong; Lou, Xiaoding; Zhao, Zujin; Tang, Ben Zhong Type I photosensitizers based on phosphindole oxide for photodynamic therapy: apoptosis and autophagy induced by endoplasmic reticulum stress Chemical Science, 2020, 11, 3405-3417 |
1557429 | CIF | C33 H27 N2 O2 P | P -1 | 9.1957; 10.841; 13.3381 100.85; 100.343; 93.057 | 1279.46 | Zhuang, Zeyan; Dai, Jun; Yu, Maoxing; Li, Jianqing; Shen, Pingchuan; Hu, Rong; Lou, Xiaoding; Zhao, Zujin; Tang, Ben Zhong Type I photosensitizers based on phosphindole oxide for photodynamic therapy: apoptosis and autophagy induced by endoplasmic reticulum stress Chemical Science, 2020, 11, 3405-3417 |
1557430 | CIF | C228 H104 B4 Cl4 F96 N12 O2 Pd2 | C 1 2/c 1 | 40.6116; 14.3027; 43.1791 90; 108.163; 90 | 23831.1 | Martí-Centelles, Vicente; Spicer, Rebecca L.; Lusby, Paul J. Non-covalent allosteric regulation of capsule catalysis Chemical Science, 2020, 11, 3236-3240 |
1557435 | CIF | C20 H19 B N2 O5 | P 1 21/c 1 | 9.8085; 8.9262; 21.7277 90; 99.222; 90 | 1877.73 | Williams, Alexander F.; White, Andrew J. P.; Spivey, Alan C.; Cordier, Christopher J. meta-Selective C‒H functionalisation of aryl boronic acids directed by a MIDA-derived boronate ester Chemical Science, 2020, 11, 3301-3306 |
1557437 | CIF | C172 H168 Ca F21 N24 O30 Rh6 S7 | P 63 | 23.302; 23.302; 21.347 90; 90; 120 | 10038 | Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin s-Block metal ions induce structural transformations between figure-eight and double trefoil knots Chemical Science, 2020, 11, 1226-1232 |
1557438 | CIF | C333 H250 F35 K2 N99 O100 Rh12 S7 | P -1 | 22.5096; 25.221; 39.36 72.977; 89.886; 76.76 | 20747 | Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin s-Block metal ions induce structural transformations between figure-eight and double trefoil knots Chemical Science, 2020, 11, 1226-1232 |
1557439 | CIF | C170 H185 F24 N24 O34.5 Rh6 S8 Sr | P 63 | 22.673; 22.673; 20.482 90; 90; 120 | 9118 | Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin s-Block metal ions induce structural transformations between figure-eight and double trefoil knots Chemical Science, 2020, 11, 1226-1232 |
1557440 | CIF | C173 H189 F24 N24 O37.5 Rh6 S8 Sr | P 63 | 22.564; 22.564; 20.375 90; 90; 120 | 8984 | Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin s-Block metal ions induce structural transformations between figure-eight and double trefoil knots Chemical Science, 2020, 11, 1226-1232 |
1557441 | CIF | C190 H252 Ba2 F30 N24 O60 Rh6 S14 | C 1 2/c 1 | 72.911; 20.9282; 33.246 90; 106.419; 90 | 48661 | Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin s-Block metal ions induce structural transformations between figure-eight and double trefoil knots Chemical Science, 2020, 11, 1226-1232 |
1557442 | CIF | C16 H20 N2 Ni O2 | P 1 21/n 1 | 14.557; 10.2366; 8.2137 90; 141.27; 90 | 765.8 | Fisher, Katherine J.; Feuer, Margalit L.; Lant, Hannah M. C.; Mercado, Brandon Q.; Crabtree, Robert H.; Brudvig, Gary W. Concerted proton-electron transfer oxidation of phenols and hydrocarbons by a high-valent nickel complex. Chemical science, 2020, 11, 1683-1690 |
1557443 | CIF | C20 H28 N2 Ni O6 | P 1 21/n 1 | 8.3939; 14.9329; 8.7611 90; 108.791; 90 | 1039.63 | Fisher, Katherine J.; Feuer, Margalit L.; Lant, Hannah M. C.; Mercado, Brandon Q.; Crabtree, Robert H.; Brudvig, Gary W. Concerted proton-electron transfer oxidation of phenols and hydrocarbons by a high-valent nickel complex. Chemical science, 2020, 11, 1683-1690 |
1557444 | CIF | C31 H35 F6 N5 Ni O2 P | I 1 2/a 1 | 22.4997; 8.4913; 17.7726 90; 111.646; 90 | 3156 | Fisher, Katherine J.; Feuer, Margalit L.; Lant, Hannah M. C.; Mercado, Brandon Q.; Crabtree, Robert H.; Brudvig, Gary W. Concerted proton-electron transfer oxidation of phenols and hydrocarbons by a high-valent nickel complex. Chemical science, 2020, 11, 1683-1690 |
1557445 | CIF | C14 H8 S2 | P -1 | 5.8903; 7.8065; 11.6922 90.458; 101.223; 93.037 | 526.52 | Wang, Chengyuan; Hashizume, Daisuke; Nakano, Masahiro; Ogaki, Takuya; Takenaka, Hiroyuki; Kawabata, Kohsuke; Takimiya, Kazuo “Disrupt and induce” intermolecular interactions to rationally design organic semiconductor crystals: from herringbone to rubrene-like pitched π-stacking Chemical Science, 2020, 11, 1573-1580 |
1557446 | CIF | C20 H14 S4 | P 1 21/c 1 | 7.45474; 16.2651; 6.76866 90; 90.98; 90 | 820.59 | Wang, Chengyuan; Hashizume, Daisuke; Nakano, Masahiro; Ogaki, Takuya; Takenaka, Hiroyuki; Kawabata, Kohsuke; Takimiya, Kazuo “Disrupt and induce” intermolecular interactions to rationally design organic semiconductor crystals: from herringbone to rubrene-like pitched π-stacking Chemical Science, 2020, 11, 1573-1580 |
1557447 | CIF | C16 H12 S4 | P 1 21/c 1 | 7.6311; 17.4783; 5.2771 90; 91.18; 90 | 703.7 | Wang, Chengyuan; Hashizume, Daisuke; Nakano, Masahiro; Ogaki, Takuya; Takenaka, Hiroyuki; Kawabata, Kohsuke; Takimiya, Kazuo “Disrupt and induce” intermolecular interactions to rationally design organic semiconductor crystals: from herringbone to rubrene-like pitched π-stacking Chemical Science, 2020, 11, 1573-1580 |
1557448 | CIF | C26 H26 | P 1 21 1 | 9.423; 10.032; 11.391 90; 104.61; 90 | 1042 | Lei, Guangyue; Zhang, Hanwen; Chen, Bin; Xu, Meichen; Zhang, Guozhu Copper-catalyzed enantioselective arylalkynylation of alkenes. Chemical science, 2020, 11, 1623-1628 |
1557449 | CIF | C55 H72 Cl F3 N3 O3 P S | P -1 | 11.0592; 12.9006; 18.7834 98.063; 91.131; 103.315 | 2578.25 | Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S. Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications Chemical Science, 2020, 11, 1975-1984 |
1557450 | CIF | C59 H80 Cl15 Ga3 N3 P | P 1 21/c 1 | 19.16275; 13.46701; 28.2924 90; 94.584; 90 | 7277.92 | Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S. Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications Chemical Science, 2020, 11, 1975-1984 |
1557451 | CIF | C57 H76 N3 P | P 1 21/c 1 | 18.56527; 11.96597; 22.85445 90; 101.614; 90 | 4973.19 | Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S. Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications Chemical Science, 2020, 11, 1975-1984 |
1557452 | CIF | C54 H72 Cl8 Ga2 N3 P | P b c a | 24.13916; 18.9021; 26.08922 90; 90; 90 | 11904 | Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S. Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications Chemical Science, 2020, 11, 1975-1984 |
1557453 | CIF | C54 H72 Cl4 Ga N3 P | P 1 21/c 1 | 11.5123; 12.8811; 37.2397 90; 97.724; 90 | 5472.21 | Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S. Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications Chemical Science, 2020, 11, 1975-1984 |
1557454 | CIF | C54 H72 N3 P | P 1 21/n 1 | 12.5627; 15.9337; 23.6169 90; 93.554; 90 | 4718.31 | Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S. Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications Chemical Science, 2020, 11, 1975-1984 |
1557455 | CIF | C115 H154 Cl10 Ga2 N6 P2 | C 1 2/c 1 | 40.7612; 12.3237; 23.4798 90; 101.398; 90 | 11562 | Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S. Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications Chemical Science, 2020, 11, 1975-1984 |
1557456 | CIF | C46 H88 Ag2 Li4 N6 O2 | P -1 | 8.3861; 11.5994; 14.05 86.881; 79.282; 83.876 | 1334.35 | Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu Lipshutz-type bis(amido)argentates for directed ortho argentation Chemical Science, 2020, 11, 1855-1861 |
1557457 | CIF | C36 H72 Ag2 Li2 N4 | C 1 2/c 1 | 22.1326; 8.3936; 22.8868 90; 109.561; 90 | 4006.34 | Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu Lipshutz-type bis(amido)argentates for directed ortho argentation Chemical Science, 2020, 11, 1855-1861 |
1557458 | CIF | C42 H56 Ag Li N2 O3 | P 1 21/n 1 | 12.4986; 14.8962; 21.7554 90; 93.742; 90 | 4041.82 | Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu Lipshutz-type bis(amido)argentates for directed ortho argentation Chemical Science, 2020, 11, 1855-1861 |
1557459 | CIF | C56 H84 Ag2 Li2 N4 O2 | P 1 21/c 1 | 13.3743; 18.2477; 22.9463 90; 103.316; 90 | 5449.49 | Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu Lipshutz-type bis(amido)argentates for directed ortho argentation Chemical Science, 2020, 11, 1855-1861 |
1557502 | CIF | C42 H56 Cl6 Fe2 N2 O12 | P 1 21/n 1 | 10.7583; 20.7341; 12.2345 90; 101.16; 90 | 2677.47 | Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules Chemical Science, 2020, 11, 3610-3618 |
1557503 | CIF | C42 H56 Cl6 Fe2 N2 O12 | P 1 21/n 1 | 10.866; 21.1945; 12.2707 90; 101.413; 90 | 2770.1 | Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules Chemical Science, 2020, 11, 3610-3618 |
1557504 | CIF | C42 H56 Cl6 Fe2 N2 O12 | P 1 21/n 1 | 10.874; 20.9284; 12.2372 90; 101.859; 90 | 2725.4 | Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules Chemical Science, 2020, 11, 3610-3618 |
1557505 | CIF | C42 H56 Cl6 Fe2 N2 O12 | P 1 21/n 1 | 10.9375; 21.278; 12.2835 90; 100.818; 90 | 2807.9 | Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules Chemical Science, 2020, 11, 3610-3618 |
1557506 | CIF | C140 H104 Cu4 N8 O20 | P -1 | 14.987; 16.858; 17.478 116.53; 107.31; 93.21 | 3679 | Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L. On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra Chemical Science, 2020, 11, 3664-3671 |
1557507 | CIF | C218 H138 Cu8 N6 O48 | P -1 | 13.914; 20.891; 21.446 71.94; 87.87; 81.2 | 5857 | Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L. On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra Chemical Science, 2020, 11, 3664-3671 |
1557508 | CIF | C116 H84 Cu4 N4 O24 | P 1 21/c 1 | 14.0177; 28.7314; 17.0738 90; 110.611; 90 | 6436.3 | Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L. On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra Chemical Science, 2020, 11, 3664-3671 |
1557509 | CIF | C53 H31 Cu2 N O12 | I 1 2/m 1 | 25.8186; 22.6806; 27.2079 90; 109.69; 90 | 15000.9 | Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L. On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra Chemical Science, 2020, 11, 3664-3671 |
1557510 | CIF | C106 H60 Cu4 O24 | C 1 2/m 1 | 19.687; 28.163; 10.475 90; 97.91; 90 | 5753 | Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L. On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra Chemical Science, 2020, 11, 3664-3671 |
1557511 | CIF | C108 H72 Cu4 O24 S4 | C 1 2/c 1 | 14.151; 32.563; 26.766 90; 102.26; 90 | 12052 | Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L. On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra Chemical Science, 2020, 11, 3664-3671 |
1557512 | CIF | C168 H124 Cu4 N12 O20 | P 1 21/n 1 | 20.979; 21.168; 23.76 90; 108.37; 90 | 10014 | Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L. On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra Chemical Science, 2020, 11, 3664-3671 |
1557513 | CIF | C16 H21 N2 O0.1 P | P n m a | 8.613; 17.7; 9.511 90; 90; 90 | 1450 | Zhang, Jingjing; Yang, Jin-Dong; Cheng, Jin-Pei Diazaphosphinanes as hydride, hydrogen atom, proton or electron donors under transition-metal-free conditions: thermodynamics, kinetics, and synthetic applications Chemical Science, 2020, 11, 3672-3679 |
1557531 | CIF | C21 Al F36 N O10 W | P 4/n :2 | 13.699; 13.699; 9.5293 90; 90; 90 | 1788.29 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557532 | CIF | C30 Al2 F55 Mo O12 | P a -3 | 17.285; 17.285; 17.285 90; 90; 90 | 5164.3 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557533 | CIF | C22 Al F36 Mo O10 | P 4/n :2 | 13.759; 13.759; 9.5821 90; 90; 90 | 1813.99 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557534 | CIF | C30 Al2 F55 O12 W | P a -3 | 17.3168; 17.3168; 17.3168 90; 90; 90 | 5192.82 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557535 | CIF | C21 Al F36 Mo N O10 | P 4/n :2 | 13.7152; 13.7152; 9.5418 90; 90; 90 | 1794.88 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557536 | CIF | C36 Al2 F73 O12 W | P -1 | 11.5888; 11.5986; 12.7755 82.965; 67.136; 87.863 | 1570.27 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557537 | CIF | C32 Al2 Cl3 F55 O14 W2 | P -1 | 11.3269; 12.2795; 23.4349 76.883; 86.161; 66.485 | 2909.8 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557538 | CIF | C46 Al2 F72 I3 Mo3 O22 | P 1 21/n 1 | 13.9703; 28.8124; 20.6169 90; 90.443; 90 | 8298.4 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557539 | CIF | C30 Al2 F55 I O12 W | P -1 | 10.5119; 12.5617; 21.1226 85.595; 76.545; 78.485 | 2656.7 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557540 | CIF | C68 Al4 F128 O26 W2 | P -1 | 15.848; 17.229; 22.395 94.072; 102.24; 101.653 | 5811.1 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557541 | CIF | C22 Al F36 I O10 W | P 1 21/c 1 | 16.438; 28.3511; 17.5878 90; 110.764; 90 | 7664.2 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557542 | CIF | C96 Al6 F165 I6 Mo6 O42 | P -1 | 13.385; 21.4285; 31.305 85.822; 81.782; 83.84 | 8820.3 | Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals Chemical Science, 2020, 11, 3592-3603 |
1557543 | CIF | C57 H88 N2 O | P 1 21/n 1 | 16.2198; 10.77; 28.9971 90; 96.1; 90 | 5036.7 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
1557544 | CIF | C71 H94 Mg2 N8 | P 1 21/c 1 | 12.8246; 21.5786; 24.2161 90; 103.493; 90 | 6516.52 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
1557545 | CIF | C49 H60 Mg2 N6 | P 1 21/c 1 | 12.4858; 12.0704; 31.1338 90; 92.762; 90 | 4686.68 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
1557546 | CIF | C137.5 H189.63 I0.04 Mg2 N4 O0.13 | P 1 21/n 1 | 18.2067; 26.3297; 25.8355 90; 105.806; 90 | 11916.7 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
1557547 | CIF | C117 H144 Mg4 N12 O4 | P -1 | 15.1058; 19.0783; 20.0582 85.762; 88.909; 66.998 | 5306.17 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
1557548 | CIF | C70 H86 Mg2 N8 | C 1 2/c 1 | 18.7699; 15.7829; 22.8274 90; 109.172; 90 | 6387.4 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
1557549 | CIF | C57 H76 Mg2 N6 | P 1 21/c 1 | 18.7194; 11.3129; 26.0645 90; 103.791; 90 | 5360.57 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
1557550 | CIF | C57 H87 I Mg N2 O | P -1 | 10.437; 14.8235; 18.7188 84.547; 75.886; 71.426 | 2661.85 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
1557551 | CIF | C151 H208 Mg4 N12 O6 | P -1 | 17.919; 19.6004; 20.9467 79.292; 75.685; 86.86 | 7004 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
1557552 | CIF | C134 H184 Mg4 N12 O12 | P 1 21/c 1 | 15.48; 15.114; 27.505 90; 103.08; 90 | 6268 | Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation Chemical Science, 2020, 11, 3516-3522 |
1557570 | CIF | C20 H18 N2 O5 | P -1 | 8.27; 9.1848; 12.4194 71.619; 82.065; 79.191 | 876.19 | Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R. Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction Chemical Science, 2020, 11, 3569-3573 |
1557571 | CIF | C44 H44 N4 O11 | P 21 21 21 | 10.9162; 11.3807; 31.809 90; 90; 90 | 3951.8 | Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R. Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction Chemical Science, 2020, 11, 3569-3573 |
1557572 | CIF | C8 H8 O5 | P 1 21 1 | 9.2321; 18.768; 18.876 90; 93.72; 90 | 3263.7 | Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R. Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction Chemical Science, 2020, 11, 3569-3573 |
1557580 | CIF | C15 H12 N4 O3 S | P 21 21 21 | 6.4901; 13.5853; 17.2054 90; 90; 90 | 1517 | Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins Chemical Science, 2020, 11, 3852-3861 |
1557581 | CIF | C25 H21 Cl N2 O3 | P 21 21 21 | 6.2023; 15.1707; 23.3424 90; 90; 90 | 2196.36 | Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins Chemical Science, 2020, 11, 3852-3861 |
1557582 | CIF | C18 H14 Br2 N4 O3 | P 1 21 1 | 7.6364; 11.6851; 11.5473 90; 104.259; 90 | 998.65 | Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins Chemical Science, 2020, 11, 3852-3861 |
1557583 | CIF | C19 H15 F N4 O3 | P 21 21 21 | 10.3148; 11.9114; 14.6673 90; 90; 90 | 1802.08 | Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins Chemical Science, 2020, 11, 3852-3861 |
1557584 | CIF | C25 H21 Cl N2 O3 | P 21 21 21 | 6.6447; 14.3101; 22.5008 90; 90; 90 | 2139.5 | Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins Chemical Science, 2020, 11, 3852-3861 |
1557585 | CIF | C37 H61 Eu N8 O15 | F d d d :2 | 18.1194; 20.3557; 43.9834 90; 90; 90 | 16222.5 | Hewitt, Sarah H.; Macey, Georgina; Mailhot, Romain; Elsegood, Mark R. J.; Duarte, Fernanda; Kenwright, Alan M.; Butler, Stephen J. Tuning the anion binding properties of lanthanide receptors to discriminate nucleoside phosphates in a sensing array Chemical Science, 2020, 11, 3619-3628 |
1557586 | CIF | C22 H18 Br Cl0 N O2 | P 21 21 21 | 5.8675; 12.4208; 24.4967 90; 90; 90 | 1785.3 | Shen, Bin; He, Qianwen; Dong, Shunxi; Liu, Xiaohua; Feng, Xiaoming A chiral cobalt(ii) complex catalyzed enantioselective aza-Piancatelli rearrangement/Diels‒Alder cascade reaction Chemical Science, 2020, 11, 3862-3867 |
1557587 | CIF | C11 H10 Br N O | P -1 | 6.732; 7.228; 12.0162 80.831; 86.517; 62.902 | 513.81 | Ikeda, Hideaki; Nishi, Kohei; Tsurugi, Hayato; Mashima, Kazushi Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine Chemical Science, 2020, 11, 3604-3609 |
1557598 | CIF | C18 H18 F3 N O4 | P 21 21 21 | 10.186; 11.3558; 15.5296 90; 90; 90 | 1796.31 | Zhang, Shuyue; Greenhalgh, Mark D.; Slawin, Alexandra M. Z.; Smith, Andrew D. Tandem sequential catalytic enantioselective synthesis of highly-functionalised tetrahydroindolizine derivatives Chemical Science, 2020, 11, 3885-3892 |
1557603 | CIF | C21 H18 N2 O2 S | C 1 2/c 1 | 17.4822; 9.78677; 20.9912 90; 103.576; 90 | 3491.13 | Li, Guofeng; Zhao, Man; Xie, Junqiu; Yao, Ying; Mou, Lingyun; Zhang, Xiaowei; Guo, Xiaomin; Sun, Wangsheng; Wang, Zheng; Xu, Jiecheng; Xue, Jianzhong; Hu, Tao; Zhang, Ming; Li, Min; Hong, Liang Efficient synthesis of cyclic amidine-based fluorophores via 6π-electrocyclic ring closure Chemical Science, 2020, 11, 3586-3591 |
1557604 | CIF | C20 H44 Cl2 N2 O2 P2 U | P 1 21/c 1 | 12.7105; 28.115; 8.1727 90; 105.391; 90 | 2815.8 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
1557605 | CIF | C18 H40 Cl2 N2 O2 P2 U | P 1 21/c 1 | 14.48; 14.59; 12.5668 90; 102.29; 90 | 2594.1 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
1557606 | CIF | C40 H88 Cl4 N4 O4 P4 Pd2 U2 | P c c n | 16.3226; 22.813; 14.7718 90; 90; 90 | 5500.5 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
1557607 | CIF | C44 H96 Cl4 N4 O6 P4 Pt3 U2 | C 1 2/c 1 | 12.663; 21.4809; 23.0838 90; 99.354; 90 | 6195.6 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
1557608 | CIF | C22 H48 Cl2 N2 Ni O3 P2 U | P 1 21/n 1 | 11.3508; 12.914; 20.597 90; 95.165; 90 | 3006.9 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
1557609 | CIF | C44 H96 Cl4 N4 Ni2 O5 P4 U2 | P 1 21/n 1 | 14.5223; 15.8953; 27.339 90; 103.728; 90 | 6130.6 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
1557610 | CIF | C40 H63 Cl2 N2 O3 P3 Pd U | P -1 | 12.208; 12.209; 17.048 108.557; 90.701; 108.839 | 2261 | Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands Chemical Science, 2020, 11, 7585-7592 |
1557613 | CIF | C22 H28 O5 S | P -1 | 7.3975; 10.7485; 13.1441 92.571; 96.25; 97.449 | 1028.29 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
1557614 | CIF | C15 H22 O3 | P 1 21/n 1 | 7.6688; 22.4305; 15.4747 90; 101.329; 90 | 2610.02 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro–Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
1557615 | CIF | C12 H20 O2 | P 1 21/c 1 | 7.1285; 11.9273; 13.4833 90; 104.629; 90 | 1109.24 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
1557616 | CIF | C15 H20 O3 | P -1 | 7.2165; 8.3504; 11.317 82.649; 76.258; 68.964 | 617.61 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
1557617 | CIF | C23 H28 N2 O3 S | P 1 21/c 1 | 10.3539; 19.9619; 11.8443 90; 113.384; 90 | 2246.95 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
1557618 | CIF | C22 H30 N2 O4 S | P 1 21/n 1 | 9.961; 17.5295; 13.2899 90; 101.667; 90 | 2272.62 | Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence Chemical Science, 2020, 11, 3878-3884 |
1557625 | CIF | C48 H55 Au F6 N4 O11 S2 | P 21 21 21 | 9.1199; 23.4191; 23.6083 90; 90; 90 | 5042.3 | Reid, Jolene P.; Hu, Mingyou; Ito, Susumu; Huang, Banruo; Hong, Cynthia M.; Xiang, Hengye; Sigman, Matthew S.; Toste, F. Dean Strategies for remote enantiocontrol in chiral gold(iii) complexes applied to catalytic enantioselective γ,δ-Diels‒Alder reactions Chemical Science, 2020, 11, 6450-6456 |
1557626 | CIF | C21 H9 N3 O6 Ti | P a -3 | 20.9953; 20.9953; 20.9953 90; 90; 90 | 9254.8 | Cao, Jing; Ma, Wenjie; Lyu, Kangjie; Zhuang, Lin; Cong, Hengjiang; Deng, Hexiang Twist and sliding dynamics between interpenetrated frames in Ti-MOF revealing high proton conductivity Chemical Science, 2020, 11, 3978-3985 |
Back to the search form
Your own data is not in the COD? Deposit it, thanks!