Crystallography Open Database

Result: there are 688 entries in the selection

Switch to the old layout of the page

Download 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

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 7 | Next 100 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1557098 CIFC42 H102 K N3 O12 Si6 TbP 1 21/n 111.1324; 27.081; 21.775
90; 103.924; 90
6371.8Ryan, 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 CIFC78 H190 Gd2 K2 N6 O21 Si12C 1 2/c 125.507; 18.806; 25.726
90; 103.21; 90
12014Ryan, 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 CIFC42 H102 K N3 O12 Si6 YP 1 21/n 111.0774; 27.0905; 21.7959
90; 104; 90
6346.5Ryan, 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 CIFC78 H190 Ho2 K2 N6 O21 Si12C 1 2/c 125.514; 18.8; 25.712
90; 103.167; 90
12009Ryan, 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 CIFC104 H96 B4 F16 N8 O4 Pd2I 1 2/a 128.36; 12.35285; 27.666
90; 94.6541; 90
9660.2Lewis, 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 CIFC123 H119 B4 F16 N17 O9 Pd2C 1 2/c 123.2193; 15.8896; 38.7298
90; 112.281; 90
13222.3Lewis, 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 CIFC16 H19 I N2P 1 21/c 16.29025; 7.62301; 32.0065
90; 90.1584; 90
1534.73Guo, 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 CIFC64 H87 I3 N5 O2P -114.6729; 15.6807; 16.4518
85.945; 73.88; 62.636
3222.3Guo, 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 CIFC17 H18 I N2P 21 21 216.9063; 7.9318; 30.157
90; 90; 90
1651.98Guo, 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 CIFC73 H92 N5 O2 UP -113.2857; 13.9411; 20.5686
103.573; 95.666; 116.252
3230.4Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557111 CIFC75 H88 N8 UP -113.1219; 13.5561; 20.3099
78.109; 76.264; 68.201
3230.5Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557112 CIFC76 H99 N6 O P UP 1 21/c 125.884; 13.889; 21.315
90; 110.09; 90
7197Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557113 CIFC75 H96 N6 UP 1 21/n 114.7113; 12.979; 36.748
90; 94.521; 90
6994.8Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557114 CIFC82 H101 N7 O UP -113.1812; 15.8571; 19.6743
110.71; 90.48; 105.002
3692.6Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557115 CIFC33 H26 O2P 21 21 2111.3659; 11.9259; 17.9314
90; 90; 90
2430.58Liu, 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 CIFC64 H88P -114.635; 18.1373; 22.0161
79.631; 75.201; 74.12
5396.2Storey, 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 CIFC61 H39 B F24 N7 RhP -112.9083; 14.2464; 20.148
74.898; 79.351; 89.459
3512.7Storey, 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 CIFC67 H62 B F24 N5 RhP -111.7452; 16.7896; 18.5777
84.062; 73.668; 70.038
3304.3Storey, 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 CIFC32 H16 F8P -110.7497; 11.175; 11.5688
96.962; 96.945; 116.711
1207.93Storey, 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 CIFC60 H51 B Cl2 F24 N5 RhC 1 c 119.4406; 17.1714; 19.516
90; 103.079; 90
6345.86Storey, 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 CIFC54 H37 B F24 N5 RhC 1 2/c 116.95902; 18.45666; 34.7576
90; 98.7133; 90
10753.8Storey, 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 CIFC68 H45 B F25 N5 O RhP -113.01044; 20.05043; 26.99316
90.7652; 97.9088; 106.636
6672.31Storey, 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 CIFC21 H20 O6P 21 21 218.6977; 9.9164; 20.6241
90; 90; 90
1778.83Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557124 CIFC37 H32 Br2 O9P 1 21/c 115.4799; 12.7561; 17.7032
90; 110.471; 90
3275Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557125 CIFC20 H20 O6P 1 21/c 111.1979; 12.5205; 24.904
90; 93.401; 90
3485.5Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557126 CIFC18 H16 O5P 1 21 111.2987; 10.6941; 11.9582
90; 90.723; 90
1444.79Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557127 CIFC18 H18 O7P 1 21/n 113.6526; 9.772; 24.8831
90; 101.015; 90
3258.6Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557128 CIFC27 H29 N O8P 1 21 110.1038; 12.0566; 10.4153
90; 97.827; 90
1256.95Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557129 CIFC17 H20 O6P 1 21 17.091; 16.2621; 13.2704
90; 92.494; 90
1528.82Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557130 CIFC27 H29 N O8C 1 2 126.9187; 7.6682; 12.9814
90; 108.271; 90
2544.5Cole, Charles J. F.; Fuentes, Lilia; Snyder, Scott A.
Asymmetric pyrone Diels‒Alder reactions enabled by dienamine catalysis
Chemical Science, 2020, 11, 2175-2180
1557131 CIFC6 H5 D N2P b c a6.0431; 13.3857; 14.3592
90; 90; 90
1161.53Yang, 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 CIFIn8 Ir1.5 S5.25P 3 1 m13.9378; 13.9378; 8.2316
90; 90; 120
1384.9Khoury, 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 CIFC18 H20 Cl N3 O PdP -17.5074; 11.2005; 11.2581
70.42; 78.131; 84.462
872.46Czyz, 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 CIFC100 H102 Au4 P2 Ru2 S8P 1 21/c 113.9904; 14.295; 48.384
90; 94.664; 90
9644.4Sun, 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 CIFC22 H12 F6 N2 O3P 1 21/n 110.7749; 15.2475; 12.314
90; 108.515; 90
1918.4Malla, 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 CIFC58 H62 N6 O13 Zn2P 1 21/c 115.21; 16.731; 23.716
90; 104.529; 90
5842Fu, 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 CIFC20 H30 N2 O2P 1 21/c 111.012; 16.138; 11.225
90; 96.899; 90
1980Chen, 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 CIFC19 H29 N3 O2I 1 2/a 117.03; 10.58; 22.26
90; 103.23; 90
3904Chen, 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 CIFC101 H48 F40 N12 Ni O7P n a 2127.571; 19.7599; 19.1951
90; 90; 90
10457.5Li, 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 CIFC89.5 H19 Cl Cu F40 N8 Ni O3C 1 2/c 147.886; 13.8742; 28.061
90; 119.602; 90
16210Li, 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 CIFC89 H22 F40 N8 O3P -111.6188; 14.403; 26.7956
82.937; 77.65; 70.954
4133.7Li, 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 CIFC97 H32 F40 N12 Ni O3P -114.057; 14.08; 24.646
92.257; 101.581; 108.23
4511.4Li, 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 CIFC89 H18 Cu F40 N8 Ni O3P -114.0363; 14.1385; 24.8547
91.904; 101.174; 107.743
4586.3Li, 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 CIFC61 H90 Au2 Cl2 F12 N2 P2 Sb2P 1 21/n 110.4398; 18.5854; 16.9617
90; 94.354; 90
3281.5Navarro, 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 CIFC34 H50 Au Cl2 F6 N O P SbP 1 21/c 110.9121; 17.7644; 19.509
90; 104.904; 90
3654.5Navarro, 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 CIFC33 H48 Au Cl2 F6 N O2 P SbP 1 21 114.8546; 12.2517; 20.5946
90; 99.848; 90
3692.9Navarro, 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 CIFC21 H20 N4 O5P 1 21/c 115.4212; 13.4652; 9.4134
90; 102.515; 90
1908.2Navarro, 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 CIFC29 H36 Au B10 Cl2 F6 P2 SbP 1 n 110.0221; 13.3021; 14.7578
90; 95.633; 90
1957.94Navarro, 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 CIFC38 H47 Au F6 N2 O2 P SbP 1 21/c 110.7728; 11.143; 30.591
90; 98.974; 90
3627.2Navarro, 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 CIFC54 H99 Am Br3 O3 P3P c a 2128.768; 11.456; 18.185
90; 90; 90
5993Windorff, 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 CIFC54 H99 Br3 Nd O3 P3P c a 2128.7058; 11.4228; 18.1359
90; 90; 90
5946.8Windorff, 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 CIFC54 H99 Br3 Ce O3 P3P c a 2128.92; 11.434; 18.209
90; 90; 90
6021.2Windorff, 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 CIFC54 H99 Br3 La O3 P3P c a 2128.879; 11.4223; 18.2083
90; 90; 90
6006.3Windorff, 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 CIFC54 H99 Br3 O3 P3 PrP c a 2128.7155; 11.4126; 18.1299
90; 90; 90
5941.5Windorff, 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 CIFC21 H21 F O2P 1 21 16.512; 15.336; 8.7541
90; 111.502; 90
813.41Groves, 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 CIFC22 H22 O2P 21 21 219.5439; 10.5734; 17.3218
90; 90; 90
1747.97Groves, 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 CIFC25 H30 N4 O3P -16.6601; 7.4588; 23.5097
94.931; 90.774; 105.499
1120.43Shi, 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 CIFC60 H44 Mn4 N12 O52 Si W12C 1 2/c 124.8686; 23.1581; 17.7369
90; 98.907; 90
10091.7Du, 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 CIFC49 H39 Mn3 Mo12 N11 O49 PP -113.034; 15.6737; 20.2719
79.875; 88.908; 87.011
4071.1Du, 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 CIFC49 H39 Mn3 N11 O49 P W12P -113.0328; 15.6142; 20.1424
79.88; 89.029; 86.775
4028.6Du, 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 CIFC25 H22 N2 O3P 1 21 19.0919; 9.9836; 11.7719
90; 95.822; 90
1063.02Zhang, 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 CIFC25 H22 N2 O3P 1 21/n 19.6576; 13.2796; 17.3578
90; 99.745; 90
2194Zhang, 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 CIFC25 H22 N2 O3P -17.8691; 9.8641; 13.184
87.285; 85.531; 74.852
984.41Zhang, 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 CIFC2 H Cl N4P b c a11.2724; 6.279; 12.5272
90; 90; 90
886.67Schnell, 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 CIFC8 H6 N4 OP 1 21/c 110.7358; 5.14454; 14.9437
90; 105.056; 90
797.02Schnell, 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 CIFC10 H7 N5F d d 238.7645; 11.93147; 7.70847
90; 90; 90
3565.3Schnell, 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 CIFC9 H9 N7 O2 S2C 1 2/c 117.7417; 6.22991; 23.2377
90; 93.9389; 90
2562.38Schnell, 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 CIFC2 H Br N4P b c a12.7468; 5.60166; 12.9507
90; 90; 90
924.72Schnell, 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 CIFC17 H21 N5 O5C 1 2 132.663; 5.161; 11.0162
90; 94.704; 90
1850.79Schnell, 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 CIFC22 H39 Al Ge Si2P 1 21/n 19.6414; 13.3432; 19.6279
90; 95.4683; 90
2513.6Albers, Lena; Tholen, Patrik; Schmidtmann, Marc; Müller, Thomas
A germaaluminocene
Chemical Science, 2020, 11, 2982-2986
1557298 CIFC6 H12 O6P 21 21 217.7012; 7.7746; 12.6751
90; 90; 90
758.91Zhou, 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 CIFC5 H12 O4I -46.0826; 6.0826; 8.792
90; 90; 90
325.29Zhou, 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 CIFC5 H10 O5P 21 21 215.6107; 9.1858; 12.5998
90; 90; 90
649.38Zhou, 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 CIFC6 H12 O6P 21 21 218.091; 9.212; 10.056
90; 90; 90
749.5Zhou, 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 CIFC203.82 H244.63 Cl7.63 N0 O40P -111.5721; 16.6408; 26.1539
84.725; 81.758; 89.936
4962.9Payne, 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 CIFC112.95 H130.95 Cl15.56 O28P 114.334; 15.534; 16.891
69.752; 70.947; 76.995
3308.6Payne, 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 CIFC106 H124 Cl6 O20P 1 21/n 119.6983; 20.2034; 26.3162
90; 97.77; 90
10377Payne, 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 CIFC108.36 H122.64 Cl2.26 O20P 1 21/c 121.532; 19.643; 25.299
90; 90.699; 90
10699Payne, 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 CIFC116.82 H140.82 Cl8.45 O28P -114.4911; 17.0462; 27.359
72.867; 86.978; 77.872
6313.8Payne, 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 CIFC76 H74 O11P -113.0381; 16.6752; 17.4483
61.711; 79.037; 74.295
3207.14Payne, 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 CIFC226.36 H257.54 O43.98P 1 21/c 121.154; 19.669; 25.429
90; 90.27; 90
10580Payne, 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 CIFC31 H53 B Eu N5 O17P 1 21/n 113.2696; 15.8873; 18.2435
90; 93.3; 90
3839.7Breen, 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 CIFC15 H21 Cl0 N O2P 21 21 218.5161; 10.575; 15.9557
90; 90; 90
1436.93Lin, 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 CIFC8 H14 N2 O4P 1 21/c 15.6483; 9.0345; 9.1851
90; 103.599; 90
455.57Blake, 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 CIFC27 H19 N O3P 17.1378; 9.8466; 14.7942
88.9786; 79.0044; 74.6213
983.56Sasaki, 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 CIFC20 H12 SP b c n21.4461; 8.4399; 7.3436
90; 90; 90
1329.21Xu, 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 CIFC48 H36 N2 O4 SP -19.2973; 11.5371; 17.8524
99.629; 101.049; 97.562
1826.25Xu, 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 CIFC97 H78 Cl2 N4 O8 S2P -110.5796; 13.7266; 14.368
85.956; 83.941; 82.064
2051.7Xu, 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 CIFC22 H14 Au2 Fe N6P 1 21/c 110.8116; 14.4381; 14.9803
90; 96.596; 90
2322.93Chen, 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 CIFC22 H14 Au2 Fe N6P 1 21/c 110.7397; 14.1109; 14.679
90; 95.98; 90
2212.5Chen, 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 CIFC22 H14 Au2 Fe N6P 1 21/c 110.7739; 13.9861; 14.5762
90; 95.77; 90
2185.28Chen, 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 CIFC22 H14 Au2 Fe N6P -110.7701; 14.1621; 14.7425
90.082; 96.077; 90.471
2235.9Chen, 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 CIFC60 H56 B2 F8 N2 O8P 1 n 112.5252; 16.8071; 12.9207
90; 90.786; 90
2719.7Kim, 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 CIFC23 H23 N O2P 1 21/c 19.3351; 20.6304; 9.7275
90; 105.289; 90
1807.1Kim, 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 CIFC33 H28 B F4 N O2P 1 21/n 111.0604; 16.678; 15.1704
90; 100.639; 90
2750.3Kim, 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 CIFC20 H21 N O4P 1 21/c 19.2314; 19.6394; 19.9121
90; 93.605; 90
3602.9Kim, 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 CIFC17 H18 F2 O2 SP 1 21/c 18.497; 13.357; 13.775
90; 85.689; 90
1559Huang, 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 CIFC33 H29 Cl F4 O4 S2P -110.2309; 13.2445; 13.5012
66.799; 70.33; 75.627
1569.19Huang, 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 CIFC16 H14 O2P 1 21 16.2309; 7.4169; 13.0054
90; 90.1686; 90
601.03Liu, 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 CIFC102 H68 N18 O27 Zn8R -3 :H22.979; 22.979; 15.496
90; 90; 120
7086Chen, 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

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 7 | Next 100 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!