Crystallography Open Database

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Searching journal of publication like 'Chemical science' volume of publication is 11

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1552456 CIFC31 H23 F3 N2 O5P 21 21 218.97942; 10.9358; 27.051
90; 90; 90		2656.33Shu, Chang; Liu, Honglei; Slawin, Alexandra M. Z.; Carpenter-Warren, Cameron; Smith, Andrew D.
Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters
Chemical Science, 2020, 11, 241-247
1552457 CIFC28 H26 F3 N3 O2P 1 21/c 119.7387; 13.4237; 9.3356
90; 93.107; 90		2469.98Shu, Chang; Liu, Honglei; Slawin, Alexandra M. Z.; Carpenter-Warren, Cameron; Smith, Andrew D.
Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters
Chemical Science, 2020, 11, 241-247
1552458 CIFC28 H26 F3 N3 O2P 1 21 113.5575; 23.9425; 19.8418
90; 93.584; 90		6428.06Shu, Chang; Liu, Honglei; Slawin, Alexandra M. Z.; Carpenter-Warren, Cameron; Smith, Andrew D.
Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters
Chemical Science, 2020, 11, 241-247
1552504 CIFC20 H22 B NF d d 239.763; 37.788; 8.9491
90; 90; 90		13446.6Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1552505 CIFC17 H17 B Cr O3 SP 1 21/c 111.605; 9.0305; 15.7985
90; 102.127; 90		1618.72Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1552506 CIFC28 H27 B OP -18.7781; 10.9283; 12.3004
70.809; 87.538; 79.597		1095.91Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1552507 CIFC27 H27 B OC 1 c 113.441; 13.1854; 24.0772
90; 94.762; 90		4252.4Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1552508 CIFC28 H29 B OP 1 21/n 114.454; 7.2349; 21.474
90; 100.708; 90		2206.5Su, Xiaojun; Baker, J. J.; Martin, Caleb D.
Dimeric boroles: effective sources of monomeric boroles for heterocycle synthesis.
Chemical science, 2020, 11, 126-131
1552533 CIFC88 H76 F24 N14 P4 Ru2P -113.885; 17.841; 22.499
83.99; 73.932; 85.868		5320.9Smitten, Kirsty L.; Fairbanks, Simon D.; Robertson, Craig C.; Bernardino de la Serna, Jorge; Foster, Simon J.; Thomas, Jim A.
Ruthenium based antimicrobial theranostics - using nanoscopy to identify therapeutic targets and resistance mechanisms in <i>Staphylococcus aureus</i>.
Chemical science, 2020, 11, 70-79
1552713 CIFC44 H42 F18 N6 P3 S2P b a m14.8195; 20.8662; 9.5394
90; 90; 90		2949.8Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552714 CIFC78 H73 F30 N11 P5C m c 2119.886; 20.698; 20.515
90; 90; 90		8444Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552715 CIFC48 H46 F18 N6 P3P b a m14.1423; 21.9108; 9.5937
90; 90; 90		2972.79Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552716 CIFC36 H32 F24 N4 P4P 1 21/c 17.4563; 20.125; 13.948
90; 91.831; 90		2091.9Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552717 CIFC32 H28 F12 N4 P2 S2P b a m10.3821; 21.5348; 9.6558
90; 90; 90		2158.81Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552718 CIFC35 H31 F24 N5 P4P -111.2904; 16.9439; 24.966
75.157; 86.061; 86.58		4601.4Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552719 CIFC34 H30 F12 N4 P2 SP b a m10.266; 21.7433; 9.8244
90; 90; 90		2193Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552720 CIFC44 H42 F18 N6 P3 SP b a m14.8597; 21.003; 9.5902
90; 90; 90		2993.1Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552721 CIFC18 H16.5 F12 N2.5 P2 S0.5P -113.603; 13.8062; 16.0216
101.314; 111.832; 107.987		2486.3Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552722 CIFC47 H45 F18 N7 P3P b a m14.1183; 21.8905; 9.5412
90; 90; 90		2948.8Cai, Kang; Shi, Yi; Cao, Changsu; Vemuri, Suneal; Cui, Binbin; Shen, Dengke; Wu, Huang; Zhang, Long; Qiu, Yunyan; Chen, Hongliang; Jiao, Yang; Stern, Charlotte L.; Alsubaie, Fehaid M.; Xiao, Hai; Li, Jun; Stoddart, J. Fraser
Tuning radical interactions in trisradical tricationic complexes by varying host-cavity sizes.
Chemical science, 2020, 11, 107-112
1552754 CIFAl B3 Cs F O6P n a 218.064; 11.97; 7.036
90; 90; 90		679.2Liu, Hongkun; Wang, Ying; Zhang, Bingbing; Yang, Zhihua; Pan, Shilie
CsAlB3O6F: a beryllium-free deep-ultraviolet nonlinear optical material with enhanced thermal stability
Chemical Science, 2020, 11, 694-698

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