Crystallography Open Database

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Searching journal of publication like 'Chemical communications (Cambridge, England)' volume of publication is 54

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7125325 CIFC32 H37 B N PP 1 21/c 118.893; 15.0154; 20.461
90; 114.845; 90
5267.3Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125326 CIFC40 H57 B Br3 Fe N2 PP 1 21/n 113.5457; 16.1351; 18.6839
90; 95.303; 90
4066.1Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125327 CIFC70 H93 B2 Br Co N8 P2C m c e25.9634; 17.706; 29.773
90; 90; 90
13686.9Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125328 CIFC144 H168 B4 Br4 Co3 N6 O6 P4P 1 21/c 122.776; 11.6346; 27.261
90; 113.332; 90
6633.2Drover, Marcus W.; Nagata, Koichi; Peters, Jonas C.
Fusing triphenylphosphine with tetraphenylborate: introducing the 9-phosphatriptycene-10-phenylborate (PTB) anion.
Chemical communications (Cambridge, England), 2018, 54, 7916-7919
7125329 CIFC16 H12 N2 O2P -17.0483; 12.691; 14.4533
103.668; 90.921; 102.65
1222.6Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125330 CIFC19 H21 F N2 O2P -16.3592; 9.7262; 15.058
92.739; 99.147; 106.484
877.5Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125331 CIFC20 H20 N2 O3P 1 21/n 19.8482; 12.1953; 15.5327
90; 106.98; 90
1784.18Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125332 CIFC20 H23 F N2 O2P 1 21/c 111.9347; 13.0246; 12.4263
90; 112.805; 90
1780.61Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125333 CIFC32 H30 N4 O3P -110.711; 11.136; 13.512
100.641; 104.19; 113.52
1358.4Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125334 CIFC16 H16 N2 OP -111.1136; 11.2993; 12.7113
105.175; 101.292; 114.625
1313.2Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125335 CIFC17 H14 N2 O2 SP 1 21/c 17.1819; 12.909; 16.108
90; 99.316; 90
1473.7Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125336 CIFC21 H22 N2 O3I 1 2/a 113.1564; 14.1743; 20.5373
90; 93.892; 90
3821Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125337 CIFC19 H18 N2 O3P 1 21/n 19.0284; 12.6694; 14.298
90; 96.266; 90
1625.7Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125338 CIFC20 H14 N2P 1 21/c 17.0181; 7.9004; 25.5706
90; 92.661; 90
1416.25Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125339 CIFC16 H14 N2 OP 21 21 215.729; 14.295; 15.456
90; 90; 90
1265.8Mai, Shaoyu; Luo, Yixin; Huang, Xianyun; Shu, Zhenghao; Li, Bingnan; Lan, Yu; Song, Qiuling
Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 10240-10243
7125340 CIFC121 H200 N6 O4 Si4 Y2P 1 2/c 123.3487; 12.1983; 21.8684
90; 92.992; 90
6219.9Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125341 CIFC99 H176 N6 O4 Si4 Yb2P -110.9326; 12.067; 21.041
105.472; 96.265; 94.586
2641.9Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125342 CIFC107 H182 N6 O4 Si4 Yb2P 1 2/c 121.5295; 12.1512; 23.1374
90; 93.7523; 90
6040Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125343 CIFC44 H60 N2 O2I 1 2/c 113.5259; 9.785; 29.268
90; 95.506; 90
3855.8Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125344 CIFC44 H72 N2 O2P -19.6188; 9.9837; 12.2473
101.903; 98.362; 113.312
1022.59Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125345 CIFC50 H76 N3 O2 Si2 YP 1 21/c 115.3478; 16.3591; 20.5634
90; 94.045; 90
5150.1Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125346 CIFC46 H84 N3 O2 Si2 YP -110.8751; 12.0478; 20.872
105.371; 96.234; 94.373
2605.5Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125347 CIFC50 H76 N3 O2 Si2 YbP 1 21/c 115.212; 16.174; 20.7742
90; 95.218; 90
5090.1Zhuo, Zhixing; Zhang, Chen; Luo, Yunjie; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Cui, Dongmei
Stereo-selectivity switchable ROP of rac-β-butyrolactone initiated by salan-ligated rare-earth metal amide complexes: the key role of the substituents on ligand frameworks.
Chemical communications (Cambridge, England), 2018, 54, 11998-12001
7125348 CIFC14 H19 Cd Cl N9 PP 21 21 2110.7129; 12.186; 16.3333
90; 90; 90
2132.27Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125349 CIFC14 H18 Cd F N9 PC 1 2/c 118.909; 10.618; 10.507
90; 111.75; 90
1959.4Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125350 CIFC14 H19 Cd Cl N9 PP b c n16.65; 16.667; 15.809
90; 90; 90
4387Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125351 CIFC14 H18 Cd F N9 PC m c e16.172; 15.6943; 16.8867
90; 90; 90
4286Zhao, Meng-Meng; Zhou, Lin; Shi, Ping-Ping; Zheng, Xuan; Chen, Xiao-Gang; Gao, Ji-Xing; Geng, Fu-Juan; Ye, Qiong; Fu, Da-Wei
Halogen substitution effects on optical and electrical properties in 3D molecular perovskites.
Chemical communications (Cambridge, England), 2018, 54, 13275-13278
7125352 CIFC24 H20 S4P 1 21/n 17.1311; 8.3942; 17.2693
90; 95.931; 90
1028.2Phan, Ngoc-Minh; Zakharov, Lev N.; Johnson, Darren W.
Copper(ii) serves as an efficient additive for metal-directed self-assembly of over 20 thiacyclophanes.
Chemical communications (Cambridge, England), 2018, 54, 13419-13422
7125353 CIFC24 H20 S4A e a 210.8663; 8.5571; 22.5617
90; 90; 90
2097.88Phan, Ngoc-Minh; Zakharov, Lev N.; Johnson, Darren W.
Copper(ii) serves as an efficient additive for metal-directed self-assembly of over 20 thiacyclophanes.
Chemical communications (Cambridge, England), 2018, 54, 13419-13422
7125456 CIFC24 H18 Cl N O2P 1 21/n 110.9587; 7.7456; 22.4121
90; 100.151; 90
1872.6Trofimov, B. A.; Belyaeva, K. V.; Nikitina, L. P.; Mal'kina, A. G.; Afonin, A. V.; Ushakov, I. A.; Vashchenko, A. V.
Transition metal-free one-pot double C-H functionalization of quinolines with disubstituted electron-deficient acetylenes.
Chemical communications (Cambridge, England), 2018, 54, 5863-5866
7125457 CIFC21 H15 N O2 SP n a 2110.0386; 16.6863; 10.3764
90; 90; 90
1738.1Trofimov, B. A.; Belyaeva, K. V.; Nikitina, L. P.; Mal'kina, A. G.; Afonin, A. V.; Ushakov, I. A.; Vashchenko, A. V.
Transition metal-free one-pot double C-H functionalization of quinolines with disubstituted electron-deficient acetylenes.
Chemical communications (Cambridge, England), 2018, 54, 5863-5866
7125458 CIFC20 H13 N O2P 1 21/c 112.115; 16.3598; 7.7826
90; 108.183; 90
1465.5Trofimov, B. A.; Belyaeva, K. V.; Nikitina, L. P.; Mal'kina, A. G.; Afonin, A. V.; Ushakov, I. A.; Vashchenko, A. V.
Transition metal-free one-pot double C-H functionalization of quinolines with disubstituted electron-deficient acetylenes.
Chemical communications (Cambridge, England), 2018, 54, 5863-5866

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