Crystallography Open Database

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1513727 CIFC42 H34C 1 2/c 114.515; 15.214; 13.3114
90; 99.134; 90
2902.3Miyoshi, Hirokazu; Nobusue, Shunpei; Shimizu, Akihiro; Hisaki, Ichiro; Miyata, Mikiji; Tobe, Yoshito
Benz[c]indeno[2,1-a]fluorene: a 2,3-naphthoquinodimethane incorporated into an indenofluorene frame
Chemical Science, 2014, 5, 163
1513728 CIFC50 H34 Cl2 N2 O2P 1 21/c 19.251; 18.592; 22.277
90; 94.409; 90
3820Miyoshi, Hirokazu; Nobusue, Shunpei; Shimizu, Akihiro; Hisaki, Ichiro; Miyata, Mikiji; Tobe, Yoshito
Benz[c]indeno[2,1-a]fluorene: a 2,3-naphthoquinodimethane incorporated into an indenofluorene frame
Chemical Science, 2014, 5, 163
1513729 CIFC45 H40 O3P 1 21/c 18.266; 18.71; 21.637
90; 90.739; 90
3346Miyoshi, Hirokazu; Nobusue, Shunpei; Shimizu, Akihiro; Hisaki, Ichiro; Miyata, Mikiji; Tobe, Yoshito
Benz[c]indeno[2,1-a]fluorene: a 2,3-naphthoquinodimethane incorporated into an indenofluorene frame
Chemical Science, 2014, 5, 163
1513730 CIFC90 H73 ClP -18.5044; 19.248; 20.4545
82.0704; 78.1032; 82.3308
3225.9Miyoshi, Hirokazu; Nobusue, Shunpei; Shimizu, Akihiro; Hisaki, Ichiro; Miyata, Mikiji; Tobe, Yoshito
Benz[c]indeno[2,1-a]fluorene: a 2,3-naphthoquinodimethane incorporated into an indenofluorene frame
Chemical Science, 2014, 5, 163
1513731 CIFC36 H33 B F6 N11 O6.5 Pd S2P b c a17.177; 19.182; 24.723
90; 90; 90
8146Brandt, Jochen R.; Lee, Eunsung; Boursalian, Gregory B.; Ritter, Tobias
Mechanism of Electrophilic Fluorination with Pd(IV): Fluoride Capture and Subsequent Oxidative Fluoride Transfer(.)
Chemical science (Royal Society of Chemistry : 2010), 2014, 5, 169
1513732 CIFC24 H27 N3 O5P -18.9819; 10.28; 13.008
86.49; 73.036; 79.688
1130.21Zhang, Yan; Wu, Qifan; Cui, Sunliang
Rh(iii)-catalyzed C–H activation–desymmetrization of diazabicycles with arenes: facile synthesis of functionalized cyclopentenes
Chemical Science, 2014, 5, 297
1513762 CIFC34 H33 Cl3 N2 PdP 1 n 111.7926; 9.4147; 14.555
90; 101.906; 90
1581.19Huo, Ping; Liu, Wanyun; He, Xiaohui; Wei, Zhenhong; Chen, Yiwang
Substituent effects and activation mechanism of norbornene polymerization catalyzed by three-dimensional geometry α-diimine palladium complexes
Polymer Chemistry, 2014, 5, 1210
1513763 CIFC35 H35 Cl N2 PdP 1 21/n 112.0765; 19.5745; 12.7667
90; 90.899; 90
3017.6Huo, Ping; Liu, Wanyun; He, Xiaohui; Wei, Zhenhong; Chen, Yiwang
Substituent effects and activation mechanism of norbornene polymerization catalyzed by three-dimensional geometry α-diimine palladium complexes
Polymer Chemistry, 2014, 5, 1210
1513764 CIFC119 H90 Cl18 N8 Pd4P -19.4659; 18.1651; 18.9183
68.501; 75.588; 84.629
2931.4Huo, Ping; Liu, Wanyun; He, Xiaohui; Wei, Zhenhong; Chen, Yiwang
Substituent effects and activation mechanism of norbornene polymerization catalyzed by three-dimensional geometry α-diimine palladium complexes
Polymer Chemistry, 2014, 5, 1210
1513765 CIFC32 H30 Fe2 Ru Si2P -114.3465; 14.4684; 14.5968
66.44; 68.64; 86.12
2575.74Erhard, Maximilian; Lam, Kevin; Haddow, Mairi; Whittell, George R.; Geiger, William E.; Manners, Ian
Polyferrocenylsilane homopolymers and diblock copolymers with pendant ruthenocenyl groups by photocontrolled ring-opening polymerisation
Polymer Chemistry, 2014, 5, 1264
1513766 CIFC21 H20 Fe Ru SiP 1 21/c 112.4947; 8.9461; 31.2176
90; 100.039; 90
3436.04Erhard, Maximilian; Lam, Kevin; Haddow, Mairi; Whittell, George R.; Geiger, William E.; Manners, Ian
Polyferrocenylsilane homopolymers and diblock copolymers with pendant ruthenocenyl groups by photocontrolled ring-opening polymerisation
Polymer Chemistry, 2014, 5, 1264
1513767 CIFC10 H9 Br RuP 1 21/m 17.1295; 8.9916; 7.2907
90; 109.503; 90
440.56Erhard, Maximilian; Lam, Kevin; Haddow, Mairi; Whittell, George R.; Geiger, William E.; Manners, Ian
Polyferrocenylsilane homopolymers and diblock copolymers with pendant ruthenocenyl groups by photocontrolled ring-opening polymerisation
Polymer Chemistry, 2014, 5, 1264
1513791 CIFC70 H66 Cl6 O4 Os P3 SP 1 21/c 123.9712; 10.7966; 25.4621
90; 95.78; 90
6556.3Zhu, Congqing; Luo, Ming; Zhu, Qin; Zhu, Jun; Schleyer, Paul V. R.; Wu, Judy I-Chia; Lu, Xin; Xia, Haiping
Planar Möbius aromatic pentalenes incorporating 16 and 18 valence electron osmiums.
Nature communications, 2014, 5, 3265
1513792 CIFC64.5 H57 Al2 Cl12 O3 Os P3P 1 21/n 118.4337; 19.2879; 20.2958
90; 97.813; 90
7149.1Zhu, Congqing; Luo, Ming; Zhu, Qin; Zhu, Jun; Schleyer, Paul V. R.; Wu, Judy I-Chia; Lu, Xin; Xia, Haiping
Planar Möbius aromatic pentalenes incorporating 16 and 18 valence electron osmiums.
Nature communications, 2014, 5, 3265
1513793 CIFC66 H58 Cl3 O5 Os P3P 1 21/c 112.6439; 21.0196; 21.9093
90; 96.0021; 90
5790.91Zhu, Congqing; Luo, Ming; Zhu, Qin; Zhu, Jun; Schleyer, Paul V. R.; Wu, Judy I-Chia; Lu, Xin; Xia, Haiping
Planar Möbius aromatic pentalenes incorporating 16 and 18 valence electron osmiums.
Nature communications, 2014, 5, 3265
1513794 CIFC21 H29 F5 Si3P b c a11.6307; 12.5277; 33.4761
90; 90; 90
4877.7Inagaki, Yusuke; Nakamoto, Masaaki; Sekiguchi, Akira
A Diels-Alder super diene breaking benzene into C2H2 and C4H4 units.
Nature communications, 2014, 5, 3018
1513795 CIFC21 H31 F5 Si3P b c a11.6585; 12.5084; 33.328
90; 90; 90
4860.2Inagaki, Yusuke; Nakamoto, Masaaki; Sekiguchi, Akira
A Diels-Alder super diene breaking benzene into C2H2 and C4H4 units.
Nature communications, 2014, 5, 3018
1513796 CIFC21 H29 F5 Si3P c a 2119.1914; 10.6017; 23.3513
90; 90; 90
4751.1Inagaki, Yusuke; Nakamoto, Masaaki; Sekiguchi, Akira
A Diels-Alder super diene breaking benzene into C2H2 and C4H4 units.
Nature communications, 2014, 5, 3018
1513797 CIFC25 H33 F5 Si3P -19.6564; 11.3871; 12.9349
72.1; 81.25; 79.77
1324.69Inagaki, Yusuke; Nakamoto, Masaaki; Sekiguchi, Akira
A Diels-Alder super diene breaking benzene into C2H2 and C4H4 units.
Nature communications, 2014, 5, 3018
1513798 CIFC11 H15 N5 O7P 1 21 15.6548; 27.587; 8.526
90; 95.291; 90
1324.4Zhao, Hang; Guo, Xiurong; He, Shiliang; Zeng, Xin; Zhou, Xinglong; Zhang, Chaoliang; Hu, Jing; Wu, Xiaohua; Xing, Zhihua; Chu, Liangyin; He, Yang; Chen, Qianming
Complex self-assembly of pyrimido[4,5-d]pyrimidine nucleoside supramolecular structures.
Nature communications, 2014, 5, 3108

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