Crystallography Open Database

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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
1557396 CIFC30 H26 B BrP 1 21/c 116.2062; 8.1904; 17.137
90; 91.218; 90
2274.2Yuan, 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 CIFC36 H36 B BrP -18.4803; 9.1672; 19.9099
80.254; 85.195; 68.593
1419.82Yuan, 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 CIFC22 H26 B Br O2P 1 21/n 16.4265; 15.8695; 20.617
90; 97.511; 90
2084.6Yuan, 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 CIFC62 H78 B2 Br2P -19.4752; 9.8107; 15.1088
93.579; 100.145; 90.47
1379.57Yuan, 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 CIFC22 H26 B Br O2P c a 2120.7096; 6.4384; 15.5735
90; 90; 90
2076.52Yuan, 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 CIFC14 H10 B Br3P 1 21/n 113.2781; 5.936; 18.4485
90; 100.58; 90
1429.37Yuan, 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 CIFC44 H42 B2 Br2 O2P c c n42.071; 29.3977; 6.6541
90; 90; 90
8229.7Yuan, 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 CIFC28 H22 B Br OP 1 21/c 116.0697; 19.1015; 7.184
90; 99.697; 90
2173.7Yuan, 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 CIFC100 H108 B4 Br4P -18.0182; 16.5443; 17.4491
64.933; 86.117; 77.027
2042.2Yuan, 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 CIFC62 H56 B2 Br2P -19.836; 10.894; 14.514
82.02; 73.02; 71.06
1405.2Yuan, 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 CIFC64 H68 B2 Br2P -113.45; 14.624; 15.214
91.36; 92.15; 116.43
2675.1Yuan, 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 CIFC33 H27 N2 O2 PP -110.6898; 11.775; 11.9913
71.708; 65.4407; 89.239
1291.4Zhuang, 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 CIFC33 H27 N2 O2 PP -19.1957; 10.841; 13.3381
100.85; 100.343; 93.057
1279.46Zhuang, 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 CIFC228 H104 B4 Cl4 F96 N12 O2 Pd2C 1 2/c 140.6116; 14.3027; 43.1791
90; 108.163; 90
23831.1Martí-Centelles, Vicente; Spicer, Rebecca L.; Lusby, Paul J.
Non-covalent allosteric regulation of capsule catalysis
Chemical Science, 2020, 11, 3236-3240
1557435 CIFC20 H19 B N2 O5P 1 21/c 19.8085; 8.9262; 21.7277
90; 99.222; 90
1877.73Williams, 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 CIFC172 H168 Ca F21 N24 O30 Rh6 S7P 6323.302; 23.302; 21.347
90; 90; 120
10038Dang, 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 CIFC333 H250 F35 K2 N99 O100 Rh12 S7P -122.5096; 25.221; 39.36
72.977; 89.886; 76.76
20747Dang, 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 CIFC170 H185 F24 N24 O34.5 Rh6 S8 SrP 6322.673; 22.673; 20.482
90; 90; 120
9118Dang, 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 CIFC173 H189 F24 N24 O37.5 Rh6 S8 SrP 6322.564; 22.564; 20.375
90; 90; 120
8984Dang, 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 CIFC190 H252 Ba2 F30 N24 O60 Rh6 S14C 1 2/c 172.911; 20.9282; 33.246
90; 106.419; 90
48661Dang, 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 CIFC16 H20 N2 Ni O2P 1 21/n 114.557; 10.2366; 8.2137
90; 141.27; 90
765.8Fisher, 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 CIFC20 H28 N2 Ni O6P 1 21/n 18.3939; 14.9329; 8.7611
90; 108.791; 90
1039.63Fisher, 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 CIFC31 H35 F6 N5 Ni O2 PI 1 2/a 122.4997; 8.4913; 17.7726
90; 111.646; 90
3156Fisher, 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 CIFC14 H8 S2P -15.8903; 7.8065; 11.6922
90.458; 101.223; 93.037
526.52Wang, 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 CIFC20 H14 S4P 1 21/c 17.45474; 16.2651; 6.76866
90; 90.98; 90
820.59Wang, 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 CIFC16 H12 S4P 1 21/c 17.6311; 17.4783; 5.2771
90; 91.18; 90
703.7Wang, 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 CIFC26 H26P 1 21 19.423; 10.032; 11.391
90; 104.61; 90
1042Lei, Guangyue; Zhang, Hanwen; Chen, Bin; Xu, Meichen; Zhang, Guozhu
Copper-catalyzed enantioselective arylalkynylation of alkenes.
Chemical science, 2020, 11, 1623-1628
1557449 CIFC55 H72 Cl F3 N3 O3 P SP -111.0592; 12.9006; 18.7834
98.063; 91.131; 103.315
2578.25Sharma, 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 CIFC59 H80 Cl15 Ga3 N3 PP 1 21/c 119.16275; 13.46701; 28.2924
90; 94.584; 90
7277.92Sharma, 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 CIFC57 H76 N3 PP 1 21/c 118.56527; 11.96597; 22.85445
90; 101.614; 90
4973.19Sharma, 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 CIFC54 H72 Cl8 Ga2 N3 PP b c a24.13916; 18.9021; 26.08922
90; 90; 90
11904Sharma, 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 CIFC54 H72 Cl4 Ga N3 PP 1 21/c 111.5123; 12.8811; 37.2397
90; 97.724; 90
5472.21Sharma, 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 CIFC54 H72 N3 PP 1 21/n 112.5627; 15.9337; 23.6169
90; 93.554; 90
4718.31Sharma, 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 CIFC115 H154 Cl10 Ga2 N6 P2C 1 2/c 140.7612; 12.3237; 23.4798
90; 101.398; 90
11562Sharma, 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 CIFC46 H88 Ag2 Li4 N6 O2P -18.3861; 11.5994; 14.05
86.881; 79.282; 83.876
1334.35Tezuka, 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 CIFC36 H72 Ag2 Li2 N4C 1 2/c 122.1326; 8.3936; 22.8868
90; 109.561; 90
4006.34Tezuka, 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 CIFC42 H56 Ag Li N2 O3P 1 21/n 112.4986; 14.8962; 21.7554
90; 93.742; 90
4041.82Tezuka, 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 CIFC56 H84 Ag2 Li2 N4 O2P 1 21/c 113.3743; 18.2477; 22.9463
90; 103.316; 90
5449.49Tezuka, 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 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.7583; 20.7341; 12.2345
90; 101.16; 90
2677.47Chen, 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 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.866; 21.1945; 12.2707
90; 101.413; 90
2770.1Chen, 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 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.874; 20.9284; 12.2372
90; 101.859; 90
2725.4Chen, 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 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.9375; 21.278; 12.2835
90; 100.818; 90
2807.9Chen, 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 CIFC140 H104 Cu4 N8 O20P -114.987; 16.858; 17.478
116.53; 107.31; 93.21
3679Bloch, 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 CIFC218 H138 Cu8 N6 O48P -113.914; 20.891; 21.446
71.94; 87.87; 81.2
5857Bloch, 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 CIFC116 H84 Cu4 N4 O24P 1 21/c 114.0177; 28.7314; 17.0738
90; 110.611; 90
6436.3Bloch, 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 CIFC53 H31 Cu2 N O12I 1 2/m 125.8186; 22.6806; 27.2079
90; 109.69; 90
15000.9Bloch, 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 CIFC106 H60 Cu4 O24C 1 2/m 119.687; 28.163; 10.475
90; 97.91; 90
5753Bloch, 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 CIFC108 H72 Cu4 O24 S4C 1 2/c 114.151; 32.563; 26.766
90; 102.26; 90
12052Bloch, 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 CIFC168 H124 Cu4 N12 O20P 1 21/n 120.979; 21.168; 23.76
90; 108.37; 90
10014Bloch, 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 CIFC16 H21 N2 O0.1 PP n m a8.613; 17.7; 9.511
90; 90; 90
1450Zhang, 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 CIFC21 Al F36 N O10 WP 4/n :213.699; 13.699; 9.5293
90; 90; 90
1788.29Bohnenberger, 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 CIFC30 Al2 F55 Mo O12P a -317.285; 17.285; 17.285
90; 90; 90
5164.3Bohnenberger, 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 CIFC22 Al F36 Mo O10P 4/n :213.759; 13.759; 9.5821
90; 90; 90
1813.99Bohnenberger, 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 CIFC30 Al2 F55 O12 WP a -317.3168; 17.3168; 17.3168
90; 90; 90
5192.82Bohnenberger, 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 CIFC21 Al F36 Mo N O10P 4/n :213.7152; 13.7152; 9.5418
90; 90; 90
1794.88Bohnenberger, 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 CIFC36 Al2 F73 O12 WP -111.5888; 11.5986; 12.7755
82.965; 67.136; 87.863
1570.27Bohnenberger, 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 CIFC32 Al2 Cl3 F55 O14 W2P -111.3269; 12.2795; 23.4349
76.883; 86.161; 66.485
2909.8Bohnenberger, 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 CIFC46 Al2 F72 I3 Mo3 O22P 1 21/n 113.9703; 28.8124; 20.6169
90; 90.443; 90
8298.4Bohnenberger, 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 CIFC30 Al2 F55 I O12 WP -110.5119; 12.5617; 21.1226
85.595; 76.545; 78.485
2656.7Bohnenberger, 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 CIFC68 Al4 F128 O26 W2P -115.848; 17.229; 22.395
94.072; 102.24; 101.653
5811.1Bohnenberger, 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 CIFC22 Al F36 I O10 WP 1 21/c 116.438; 28.3511; 17.5878
90; 110.764; 90
7664.2Bohnenberger, 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 CIFC96 Al6 F165 I6 Mo6 O42P -113.385; 21.4285; 31.305
85.822; 81.782; 83.84
8820.3Bohnenberger, 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 CIFC57 H88 N2 OP 1 21/n 116.2198; 10.77; 28.9971
90; 96.1; 90
5036.7Yuvaraj, 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 CIFC71 H94 Mg2 N8P 1 21/c 112.8246; 21.5786; 24.2161
90; 103.493; 90
6516.52Yuvaraj, 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 CIFC49 H60 Mg2 N6P 1 21/c 112.4858; 12.0704; 31.1338
90; 92.762; 90
4686.68Yuvaraj, 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 CIFC137.5 H189.63 I0.04 Mg2 N4 O0.13P 1 21/n 118.2067; 26.3297; 25.8355
90; 105.806; 90
11916.7Yuvaraj, 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 CIFC117 H144 Mg4 N12 O4P -115.1058; 19.0783; 20.0582
85.762; 88.909; 66.998
5306.17Yuvaraj, 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 CIFC70 H86 Mg2 N8C 1 2/c 118.7699; 15.7829; 22.8274
90; 109.172; 90
6387.4Yuvaraj, 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 CIFC57 H76 Mg2 N6P 1 21/c 118.7194; 11.3129; 26.0645
90; 103.791; 90
5360.57Yuvaraj, 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 CIFC57 H87 I Mg N2 OP -110.437; 14.8235; 18.7188
84.547; 75.886; 71.426
2661.85Yuvaraj, 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 CIFC151 H208 Mg4 N12 O6P -117.919; 19.6004; 20.9467
79.292; 75.685; 86.86
7004Yuvaraj, 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 CIFC134 H184 Mg4 N12 O12P 1 21/c 115.48; 15.114; 27.505
90; 103.08; 90
6268Yuvaraj, 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 CIFC20 H18 N2 O5P -18.27; 9.1848; 12.4194
71.619; 82.065; 79.191
876.19Yelgaonkar, 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 CIFC44 H44 N4 O11P 21 21 2110.9162; 11.3807; 31.809
90; 90; 90
3951.8Yelgaonkar, 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 CIFC8 H8 O5P 1 21 19.2321; 18.768; 18.876
90; 93.72; 90
3263.7Yelgaonkar, 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 CIFC15 H12 N4 O3 SP 21 21 216.4901; 13.5853; 17.2054
90; 90; 90
1517Ding, 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 CIFC25 H21 Cl N2 O3P 21 21 216.2023; 15.1707; 23.3424
90; 90; 90
2196.36Ding, 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 CIFC18 H14 Br2 N4 O3P 1 21 17.6364; 11.6851; 11.5473
90; 104.259; 90
998.65Ding, 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 CIFC19 H15 F N4 O3P 21 21 2110.3148; 11.9114; 14.6673
90; 90; 90
1802.08Ding, 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 CIFC25 H21 Cl N2 O3P 21 21 216.6447; 14.3101; 22.5008
90; 90; 90
2139.5Ding, 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 CIFC37 H61 Eu N8 O15F d d d :218.1194; 20.3557; 43.9834
90; 90; 90
16222.5Hewitt, 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 CIFC22 H18 Br Cl0 N O2P 21 21 215.8675; 12.4208; 24.4967
90; 90; 90
1785.3Shen, 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 CIFC11 H10 Br N OP -16.732; 7.228; 12.0162
80.831; 86.517; 62.902
513.81Ikeda, 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 CIFC18 H18 F3 N O4P 21 21 2110.186; 11.3558; 15.5296
90; 90; 90
1796.31Zhang, 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 CIFC21 H18 N2 O2 SC 1 2/c 117.4822; 9.78677; 20.9912
90; 103.576; 90
3491.13Li, 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 CIFC20 H44 Cl2 N2 O2 P2 UP 1 21/c 112.7105; 28.115; 8.1727
90; 105.391; 90
2815.8Feng, 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 CIFC18 H40 Cl2 N2 O2 P2 UP 1 21/c 114.48; 14.59; 12.5668
90; 102.29; 90
2594.1Feng, 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 CIFC40 H88 Cl4 N4 O4 P4 Pd2 U2P c c n16.3226; 22.813; 14.7718
90; 90; 90
5500.5Feng, 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 CIFC44 H96 Cl4 N4 O6 P4 Pt3 U2C 1 2/c 112.663; 21.4809; 23.0838
90; 99.354; 90
6195.6Feng, 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 CIFC22 H48 Cl2 N2 Ni O3 P2 UP 1 21/n 111.3508; 12.914; 20.597
90; 95.165; 90
3006.9Feng, 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 CIFC44 H96 Cl4 N4 Ni2 O5 P4 U2P 1 21/n 114.5223; 15.8953; 27.339
90; 103.728; 90
6130.6Feng, 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 CIFC40 H63 Cl2 N2 O3 P3 Pd UP -112.208; 12.209; 17.048
108.557; 90.701; 108.839
2261Feng, 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 CIFC22 H28 O5 SP -17.3975; 10.7485; 13.1441
92.571; 96.25; 97.449
1028.29Zhang, 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 CIFC15 H22 O3P 1 21/n 17.6688; 22.4305; 15.4747
90; 101.329; 90
2610.02Zhang, 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 CIFC12 H20 O2P 1 21/c 17.1285; 11.9273; 13.4833
90; 104.629; 90
1109.24Zhang, 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 CIFC15 H20 O3P -17.2165; 8.3504; 11.317
82.649; 76.258; 68.964
617.61Zhang, 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 CIFC23 H28 N2 O3 SP 1 21/c 110.3539; 19.9619; 11.8443
90; 113.384; 90
2246.95Zhang, 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 CIFC22 H30 N2 O4 SP 1 21/n 19.961; 17.5295; 13.2899
90; 101.667; 90
2272.62Zhang, 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 CIFC48 H55 Au F6 N4 O11 S2P 21 21 219.1199; 23.4191; 23.6083
90; 90; 90
5042.3Reid, 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 CIFC21 H9 N3 O6 TiP a -320.9953; 20.9953; 20.9953
90; 90; 90
9254.8Cao, 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

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