Crystallography Open Database

Result: there are 1859 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)

Searching journal of publication like 'Chemical Communications' volume of publication is 50

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 19 | Next 100 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
7114593 CIFC32 H42 N2 NiP 1 21/n 112.4764; 36.2568; 12.7163
90; 90.223; 90
5752.2Stefan Pelties; Dirk Herrmann; Bas de Bruin; Frantisek Hartl; Robert Wolf
Selective P4 activation by an organometallic nickel(I) radical: formation of a dinuclear nickel(II) tetraphosphide and related di- and trichalcogenides
Chem.Commun., 2014, 50, 7014
7114594 CIFC26 H29 N2 NiP n m a22.8909; 11.1074; 9.0371
90; 90; 90
2297.76Stefan Pelties; Dirk Herrmann; Bas de Bruin; Frantisek Hartl; Robert Wolf
Selective P4 activation by an organometallic nickel(I) radical: formation of a dinuclear nickel(II) tetraphosphide and related di- and trichalcogenides
Chem.Commun., 2014, 50, 7014
7114595 CIFC37 H51 N2 NiP 1 21/n 19.2397; 18.6957; 21.5074
90; 93.779; 90
3707.17Stefan Pelties; Dirk Herrmann; Bas de Bruin; Frantisek Hartl; Robert Wolf
Selective P4 activation by an organometallic nickel(I) radical: formation of a dinuclear nickel(II) tetraphosphide and related di- and trichalcogenides
Chem.Commun., 2014, 50, 7014
7114596 CIFC36 H49 F6 N2 Ni O PC 1 c 112.7889; 16.8666; 16.4852
90; 94.486; 90
3545.05Stefan Pelties; Dirk Herrmann; Bas de Bruin; Frantisek Hartl; Robert Wolf
Selective P4 activation by an organometallic nickel(I) radical: formation of a dinuclear nickel(II) tetraphosphide and related di- and trichalcogenides
Chem.Commun., 2014, 50, 7014
7114597 CIFC15 H21 B F4 N2P n m a17.4172; 7.0912; 13.2491
90; 90; 90
1636.38Travis Lundrigan; T. Stanley Cameron; Alison Thompson
Activation and deprotection of F-BODIPYs using boron trihalides
Chem.Commun., 2014, 50, 7028
7114598 CIFC28 H25 N O5P 1 21/n 111.3483; 13.1679; 14.9704
90; 103.528; 90
2175.01Asif Noor; Warrick K. C. Lo; Stephen C. Moratti; James D. Crowley
CuAAC 'click' active-template synthesis of functionalised [2]rotaxanes using small exo-substituted macrocycles: how small is too small?
Chem.Commun., 2014, 50, 7044
7114599 CIFC30 H29 N O5P -110.9095; 11.1519; 11.665
76.633; 88.947; 63.197
1226.35Asif Noor; Warrick K. C. Lo; Stephen C. Moratti; James D. Crowley
CuAAC 'click' active-template synthesis of functionalised [2]rotaxanes using small exo-substituted macrocycles: how small is too small?
Chem.Commun., 2014, 50, 7044
7114600 CIFC57 H50 Ag F3 N2 O13 SP 1 n 111.0416; 21.5483; 21.3436
90; 91.7631; 90
5075.83Asif Noor; Warrick K. C. Lo; Stephen C. Moratti; James D. Crowley
CuAAC 'click' active-template synthesis of functionalised [2]rotaxanes using small exo-substituted macrocycles: how small is too small?
Chem.Commun., 2014, 50, 7044
7114601 CIFC61 H58 Ag F3 N2 O13 SP -112.3931; 12.749; 19.1316
106.432; 90.948; 108.504
2730.58Asif Noor; Warrick K. C. Lo; Stephen C. Moratti; James D. Crowley
CuAAC 'click' active-template synthesis of functionalised [2]rotaxanes using small exo-substituted macrocycles: how small is too small?
Chem.Commun., 2014, 50, 7044
7114602 CIFC124 H116 Ag2 F6 N8 O18 S2P -111.7502; 15.4683; 17.5738
108.091; 101.907; 98.189
2896.75Asif Noor; Warrick K. C. Lo; Stephen C. Moratti; James D. Crowley
CuAAC 'click' active-template synthesis of functionalised [2]rotaxanes using small exo-substituted macrocycles: how small is too small?
Chem.Commun., 2014, 50, 7044
7114603 CIFC68.1 H66.6 Mn N8 O4.2 Os P2P -113.2901; 15.2869; 18.7961
93.05; 110.232; 114.384
3176.5Eugenia V. Peresypkina; Anna M. Majcher; Michal Rams; Kira E. Vostrikova
A single chain magnet involving hexacyanoosmate
Chem.Commun., 2014, 50, 7150
7114604 CIFC22 H24 N2 SP b c a14.5278; 14.5993; 17.0361
90; 90; 90
3613.3Bin-Miao Yang; Kai Xiang; Yong-Qiang Tu; Shi-Heng Zhang; Deng-Tao Yang; Shao-Hua Wang; Fu-Ming Zhang
Spiro-fused six-membered N-heterocyclic carbene: a new scaffold toward unique properties and activities
Chem.Commun., 2014, 50, 7163
7114605 CIFC22 H25 B F4 N2P 1 21/n 19.802; 19; 11.112
90; 91.156; 90
2069Bin-Miao Yang; Kai Xiang; Yong-Qiang Tu; Shi-Heng Zhang; Deng-Tao Yang; Shao-Hua Wang; Fu-Ming Zhang
Spiro-fused six-membered N-heterocyclic carbene: a new scaffold toward unique properties and activities
Chem.Commun., 2014, 50, 7163
7114606 CIFC22 H24 Au Cl N2P 1 21/n 119.6622; 10.8065; 19.9969
90; 105.351; 90
4097.3Bin-Miao Yang; Kai Xiang; Yong-Qiang Tu; Shi-Heng Zhang; Deng-Tao Yang; Shao-Hua Wang; Fu-Ming Zhang
Spiro-fused six-membered N-heterocyclic carbene: a new scaffold toward unique properties and activities
Chem.Commun., 2014, 50, 7163
7114607 CIFC22 H24 B F3 N2P 1 21/n 18.8224; 14.8677; 14.68
90; 96.474; 90
1913.28Bin-Miao Yang; Kai Xiang; Yong-Qiang Tu; Shi-Heng Zhang; Deng-Tao Yang; Shao-Hua Wang; Fu-Ming Zhang
Spiro-fused six-membered N-heterocyclic carbene: a new scaffold toward unique properties and activities
Chem.Commun., 2014, 50, 7163
7114608 CIFC48 H56 Cl2 Cu2 N4 OP n a 2122.4845; 15.3897; 12.7631
90; 90; 90
4416.4Bin-Miao Yang; Kai Xiang; Yong-Qiang Tu; Shi-Heng Zhang; Deng-Tao Yang; Shao-Hua Wang; Fu-Ming Zhang
Spiro-fused six-membered N-heterocyclic carbene: a new scaffold toward unique properties and activities
Chem.Commun., 2014, 50, 7163
7114609 CIFC22 H24 N2P b c a12.4457; 9.7837; 28.322
90; 90; 90
3448.6Bin-Miao Yang; Kai Xiang; Yong-Qiang Tu; Shi-Heng Zhang; Deng-Tao Yang; Shao-Hua Wang; Fu-Ming Zhang
Spiro-fused six-membered N-heterocyclic carbene: a new scaffold toward unique properties and activities
Chem.Commun., 2014, 50, 7163
7114610 CIFC30 H36 Cl N2 RhP 1 21/n 111.1034; 19.4323; 13.1451
90; 112.161; 90
2626.73Bin-Miao Yang; Kai Xiang; Yong-Qiang Tu; Shi-Heng Zhang; Deng-Tao Yang; Shao-Hua Wang; Fu-Ming Zhang
Spiro-fused six-membered N-heterocyclic carbene: a new scaffold toward unique properties and activities
Chem.Commun., 2014, 50, 7163
7114611 CIFC49 H54 B Cu N4P 1 21/n 111.4316; 20.5365; 18.732
90; 105.371; 90
4240.3Valentina A. Krylova; Peter I. Djurovich; Brian L. Conley; Ralf Haiges; Matthew T. Whited; Travis J. Williams; Mark E. Thompson
Control of emission colour with N-heterocyclic carbene (NHC) ligands in phosphorescent three-coordinate Cu(I) complexes
Chem.Commun., 2014, 50, 7176
7114612 CIFC35 H36 B Cu N4P -111.595; 11.6113; 24.245
95.896; 102.601; 102.694
3068.5Valentina A. Krylova; Peter I. Djurovich; Brian L. Conley; Ralf Haiges; Matthew T. Whited; Travis J. Williams; Mark E. Thompson
Control of emission colour with N-heterocyclic carbene (NHC) ligands in phosphorescent three-coordinate Cu(I) complexes
Chem.Commun., 2014, 50, 7176
7114613 CIFC33 H34 B Cu N6P 1 21/n 119.1311; 8.4051; 19.2334
90; 107.483; 90
2949.8Valentina A. Krylova; Peter I. Djurovich; Brian L. Conley; Ralf Haiges; Matthew T. Whited; Travis J. Williams; Mark E. Thompson
Control of emission colour with N-heterocyclic carbene (NHC) ligands in phosphorescent three-coordinate Cu(I) complexes
Chem.Commun., 2014, 50, 7176
7114614 CIFC39 H50 B Cu N4P n m a16.535; 20.3273; 11.0518
90; 90; 90
3714.6Valentina A. Krylova; Peter I. Djurovich; Brian L. Conley; Ralf Haiges; Matthew T. Whited; Travis J. Williams; Mark E. Thompson
Control of emission colour with N-heterocyclic carbene (NHC) ligands in phosphorescent three-coordinate Cu(I) complexes
Chem.Commun., 2014, 50, 7176
7114615 CIFC48 H42 Cl2 Fe N8 O6P -111.666; 11.764; 18.282
78.585; 88.896; 63.247
2189Jesse V. Gavette; Christina M. Klug; Lev N. Zakharov; Matthew P. Shores; Michael M. Haley; Darren W. Johnson
Intramolecular N-HCl hydrogen bonds in the outer coordination sphere of a bipyridyl bisurea-based ligand stabilize a tetrahedral FeLCl2 complex
Chem.Commun., 2014, 50, 7173
7114616 CIFC15 H19 F6 Fe N5 O2.5 PP 1 21/c 114.361; 8.1428; 18.0294
90; 91.916; 90
2107.2Alan Kay Liang Teo; Wai Yip Fan
A novel iron complex for highly efficient catalytic hydrogen generation from the hydrolysis of organosilanes
Chem.Commun., 2014, 50, 7191
7114617 CIFC54 H73 B Cu2 F4 N4 OP 1 21/n 110.5133; 27.0087; 18.8062
90; 93.125; 90
5332.1Houssein Ibrahim; Regis Guillot; Federico Cisnetti; Arnaud Gautier
[{Cu(IPr)}2(mu-OH)][BF4]: synthesis and halide-free CuAAC catalysis
Chem.Commun., 2014, 50, 7154
7114618 CIFC21 H23 N O4P 21 21 218.8244; 10.0482; 20.7767
90; 90; 90
1842.3I. A. O'Neil; M. McConville; K. Zhou; C. Brooke; C. M. Robertson; N. G. Berry
The synthesis and structure of chiral enamine N-oxides
Chem.Commun., 2014, 50, 7336
7114619 CIFC25 H29 N O6P 21 21 2110.252; 10.869; 40.512
90; 90; 90
4514.2I. A. O'Neil; M. McConville; K. Zhou; C. Brooke; C. M. Robertson; N. G. Berry
The synthesis and structure of chiral enamine N-oxides
Chem.Commun., 2014, 50, 7336
7114620 CIFC33 H23 N O SP 1 21/c 123.642; 5.7597; 19.018
90; 105.496; 90
2495.6Chunping Ma; Bingjia Xu; Gaoyi Xie; Jiajun He; Xie Zhou; Bangyin Peng; Long Jiang; Bin Xu; Wenjing Tian; Zhenguo Chi; Siwei Liu; Yi Zhang; Jiarui Xu
An AIE-active luminophore with tunable and remarkable fluorescence switching based on the piezo and protonation-deprotonation control
Chem.Commun., 2014, 50, 7374
7114621 CIFC41 H40 Cl N O3 SP 1 21/c 125.4332; 13.2344; 10.6949
90; 96.568; 90
3576.2Chunping Ma; Bingjia Xu; Gaoyi Xie; Jiajun He; Xie Zhou; Bangyin Peng; Long Jiang; Bin Xu; Wenjing Tian; Zhenguo Chi; Siwei Liu; Yi Zhang; Jiarui Xu
An AIE-active luminophore with tunable and remarkable fluorescence switching based on the piezo and protonation-deprotonation control
Chem.Commun., 2014, 50, 7374
7114622 CIFC33 H24 Cl N O SP 1 21/c 121.1014; 9.2666; 13.5115
90; 100.062; 90
2601.4Chunping Ma; Bingjia Xu; Gaoyi Xie; Jiajun He; Xie Zhou; Bangyin Peng; Long Jiang; Bin Xu; Wenjing Tian; Zhenguo Chi; Siwei Liu; Yi Zhang; Jiarui Xu
An AIE-active luminophore with tunable and remarkable fluorescence switching based on the piezo and protonation-deprotonation control
Chem.Commun., 2014, 50, 7374
7114623 CIFC30 H12 B F15 O2P -110.6886; 11.3024; 12.794
67.05; 74.863; 83.714
1373.83Max M. Hansmann; Rebecca L. Melen; Frank Rominger; A. Stephen K. Hashmi; Douglas W. Stephan
B(C6F5)3 promoted cyclisation of internal propargyl esters: structural characterisation of 1,3-dioxolium compounds
Chem.Commun., 2014, 50, 7243
7114624 CIFC32.5 H17 B Cl F15 O2P 1 21/c 111.732; 20.805; 13.426
90; 107.896; 90
3118.5Max M. Hansmann; Rebecca L. Melen; Frank Rominger; A. Stephen K. Hashmi; Douglas W. Stephan
B(C6F5)3 promoted cyclisation of internal propargyl esters: structural characterisation of 1,3-dioxolium compounds
Chem.Commun., 2014, 50, 7243
7114625 CIFC13 H15 N O2R 3 c :H25.053; 25.053; 9.645
90; 90; 120
5242.7Xue Zhang; Yifei Li; Hui Shi; Lunan Zhang; Shanshan Zhang; Xianxiu Xu; Qun Liu
Rhodium(III)-catalyzed intramolecular amidoarylation and hydroarylation of alkyne via C-H activation: switchable synthesis of 3,4-fused tricyclic indoles and chromans
Chem.Commun., 2014, 50, 7306
7114626 CIFC34 H34 N4 O4 ZnF d d 221.494; 36.481; 7.28
90; 90; 90
5708.4Jie Zhang; Jianming Geng; Guiming Zheng; Jingcao Dai; Zhiyong Fu
Highly stable photoresponsive complex framework formation involves unusual selective hydrogenation of a pyridine derivative
Chem.Commun., 2014, 50, 7326
7114627 CIFC34 H34 N4 O4 ZnF d d 221.497; 36.708; 7.2655
90; 90; 90
5733.3Jie Zhang; Jianming Geng; Guiming Zheng; Jingcao Dai; Zhiyong Fu
Highly stable photoresponsive complex framework formation involves unusual selective hydrogenation of a pyridine derivative
Chem.Commun., 2014, 50, 7326
7114628 CIFC19 H19 N OP 1 21/c 112.0655; 7.4251; 18.788
90; 111.551; 90
1565.5Virendra Kumar Tiwari; Govind Goroba Pawar; Himanshu Sekhar Jena; Manmohan Kapur
Palladium catalyzed, heteroatom-guided C-H functionalization in the synthesis of substituted isoquinolines and dihydroisoquinolines
Chem.Commun., 2014, 50, 7322
7114629 CIFC21 H23 N OP 1 21/n 110.0609; 7.6268; 22.661
90; 102.027; 90
1700.7Virendra Kumar Tiwari; Govind Goroba Pawar; Himanshu Sekhar Jena; Manmohan Kapur
Palladium catalyzed, heteroatom-guided C-H functionalization in the synthesis of substituted isoquinolines and dihydroisoquinolines
Chem.Commun., 2014, 50, 7322
7114630 CIFC40.5 H48 Au Cl F3 N5 O3 SP -111.9536; 17.4706; 23.2795
78.685; 89.654; 71.448
4511.1Rong Cai; Dawei Wang; Yunfeng Chen; Wuming Yan; Natalie R. Geise; Sripadh Sharma; Huiyuan Li; Jeffrey L. Petersen; Minyong Li; Xiaodong Shi
Facile synthesis of fluorescent active triazapentalenes through gold-catalyzed triazole-alkyne cyclization
Chem.Commun., 2014, 50, 7303
7114631 CIFC19 H15 N3 OP b c a7.8543; 18.5471; 21.14
90; 90; 90
3079.6Rong Cai; Dawei Wang; Yunfeng Chen; Wuming Yan; Natalie R. Geise; Sripadh Sharma; Huiyuan Li; Jeffrey L. Petersen; Minyong Li; Xiaodong Shi
Facile synthesis of fluorescent active triazapentalenes through gold-catalyzed triazole-alkyne cyclization
Chem.Commun., 2014, 50, 7303
7114632 CIFC21 H17 N3 O4P 1 21/c 18.057; 22.7381; 10.3968
90; 107.446; 90
1817.1Rong Cai; Dawei Wang; Yunfeng Chen; Wuming Yan; Natalie R. Geise; Sripadh Sharma; Huiyuan Li; Jeffrey L. Petersen; Minyong Li; Xiaodong Shi
Facile synthesis of fluorescent active triazapentalenes through gold-catalyzed triazole-alkyne cyclization
Chem.Commun., 2014, 50, 7303
7114633 CIFC20 H17 Br N2 O5P -18.9971; 10.0949; 11.5631
70.132; 68.095; 80.935
915.83Victor Ceban; Piotr Putaj; Marta Meazza; Mateusz B. Pitak; Simon J. Coles; Jan Vesely; Ramon Rios
Synergistic catalysis: highly diastereoselective benzoxazole addition to Morita-Baylis-Hillman carbonates
Chem.Commun., 2014, 50, 7447
7114634 CIFC33 H41 Cl2 Fe N8 O9P 1 21/c 112.1581; 23.2662; 13.242
90; 100.424; 90
3683.98Yutaka Hitomi; Kengo Arakawa; Masahito Kodera
Synthesis, stability and reactivity of the first mononuclear nonheme oxoiron(IV) species with monoamido ligation: a putative reactive species generated from iron-bleomycin
Chem.Commun., 2014, 50, 7485
7114636 CIFC23 H17 F3 N2P 4110.77844; 10.77844; 16.0189
90; 90; 90
1860.99Xuejian Li; Di Chen; Haorui Gu; Xufeng Lin
Enantioselective synthesis of benzazepinoindoles bearing trifluoromethylated quaternary stereocenters catalyzed by chiral spirocyclic phosphoric acids
Chem.Commun., 2014, 50, 7538
7114637 CIFC67.5 H73 Cl N2 O12P 1 21 112.0918; 21.3853; 26.0509
90; 92.817; 90
6728.3Nathan L. Strutt; Huacheng Zhang; J. Fraser Stoddart
Enantiopure pillar[5]arene active domains within a homochiral metal-organic framework
Chem.Commun., 2014, 50, 7455
7114638 CIFC67 H72 N2 O12P 1 21 112.9346; 11.7299; 21.685
90; 97.077; 90
3265Nathan L. Strutt; Huacheng Zhang; J. Fraser Stoddart
Enantiopure pillar[5]arene active domains within a homochiral metal-organic framework
Chem.Commun., 2014, 50, 7455
7114639 CIFC62 H40 N4 O2P -110.8574; 14.598; 15.654
90.116; 105.115; 110.614
2229.8Takahiro Iwasaki; Tetsuya Kato; Yoichi Kobayashi; Jiro Abe
A chiral BINOL-bridged imidazole dimer possessing sub-millisecond fast photochromism
Chem.Commun., 2014, 50, 7481
7114640 CIFC20 H19 N O5P 1 21 17.4062; 7.4146; 16.172
90; 91.997; 90
887.5Weiwei Luo; Jiannan Zhao; Chengkai Yin; Xiaohua Liu; Lili Lin; Xiaoming Feng
Catalytic hetero-ene reactions of 5-methyleneoxazolines: highly enantioselective synthesis of 2,5-disubstituted oxazole derivatives
Chem.Commun., 2014, 50, 7524
7114641 CIFC18 H14 Br N O3P 1 21 111.3897; 5.3882; 13.3371
90; 106.961; 90
782.9Weiwei Luo; Jiannan Zhao; Chengkai Yin; Xiaohua Liu; Lili Lin; Xiaoming Feng
Catalytic hetero-ene reactions of 5-methyleneoxazolines: highly enantioselective synthesis of 2,5-disubstituted oxazole derivatives
Chem.Commun., 2014, 50, 7524
7114642 CIFC19 H19 Br OP 21 21 219.8879; 12.4088; 13.0415
90; 90; 90
1600.15Claudia Lalli; Pierre van de Weghe
Enantioselective Prins cyclization: BINOL-derived phosphoric acid and CuCl synergistic catalysis
Chem.Commun., 2014, 50, 7495
7114643 CIFC14 H26 K2 Ni O13 S4P -17.3428; 13.2262; 13.8832
89.836; 83.498; 77.413
1307.1Tae Hwan Noh; Jaeseong Jang; Woosik Hong; Haeri Lee; Ok-Sang Jung
Truncated trigonal prismatic tubular crystals consisting of a zeolite L-mimic metal-organic framework
Chem.Commun., 2014, 50, 7451
7114644 CIFC36 H48 Ag8 Ni2 O31 S12P -315.8928; 15.8928; 7.9116
90; 90; 120
1730.6Tae Hwan Noh; Jaeseong Jang; Woosik Hong; Haeri Lee; Ok-Sang Jung
Truncated trigonal prismatic tubular crystals consisting of a zeolite L-mimic metal-organic framework
Chem.Commun., 2014, 50, 7451
7114645 CIFC20 H17 B F2 N4P 1 21/c 110.416; 18.8213; 9.2633
90; 101.539; 90
1779.3M.C. Chang; E. Otten
Synthesis and ligand-based reduction chemistry of boron difluoride complexes with redox-active formazanate ligands
Chem.Commun., 2014, 50, 7431
7114646 CIFC33.25 H33.47 B Co F2 N4 O0.81P 1 21/n 112.2031; 17.4363; 14.4788
90; 97.446; 90
3054.8M.C. Chang; E. Otten
Synthesis and ligand-based reduction chemistry of boron difluoride complexes with redox-active formazanate ligands
Chem.Commun., 2014, 50, 7431
7114647 CIFC44 H32 B2 F16 N8 ZnP 1 21/c 128.1225; 20.6482; 15.3728
90; 93.868; 90
8906.3M.C. Chang; E. Otten
Synthesis and ligand-based reduction chemistry of boron difluoride complexes with redox-active formazanate ligands
Chem.Commun., 2014, 50, 7431
7114648 CIFC14 H22 O6P 1 21 19.8616; 8.0284; 9.9965
90; 118.639; 90
694.62Zachary A. Kasun; Laina M. Geary; Michael J. Krische
Ring expansion of cyclic 1,2-diols to form medium sized rings via ruthenium catalyzed transfer hydrogenative [4+2] cycloaddition
Chem.Commun., 2014, 50, 7545
7114649 CIFC14 H18 O4P -18.326; 10.119; 14.59
90.631; 106.543; 91.53
1177.7Zachary A. Kasun; Laina M. Geary; Michael J. Krische
Ring expansion of cyclic 1,2-diols to form medium sized rings via ruthenium catalyzed transfer hydrogenative [4+2] cycloaddition
Chem.Commun., 2014, 50, 7545
7114650 CIFC24 H23 N O3P -17.7752; 8.7771; 14.9802
102.869; 96.841; 92.197
987.31Jie Zhou; Ping Chen; Xu Wang; Yan Wang; Yi Wang; Feng Li; Minghui Yang; Yan Huang; Junsheng Yu; Zhiyun Lu
Charge-transfer-featured materials-promising hosts for fabrication of efficient OLEDs through triplet harvesting via triplet fusion
Chem.Commun., 2014, 50, 7586
7114651 CIFC30 H33 Dy N6 O12P n a 2115.081; 16.728; 13.061
90; 90; 90
3295Qing-Yuan Yang; Kai Wu; Ji-Jun Jiang; Chien-Wei Hsu; Mei Pan; Jean-Marie Lehn; Cheng-Yong Su
Pure white-light and yellow-to-blue emission tuning in single crystals of Dy(III) metal-organic frameworks
Chem.Commun., 2014, 50, 7702
7114652 CIFC9 H30 Cl Er N3 O17 P3P -19.0898; 9.1926; 15.1167
88.3976; 75.9926; 75.87
1187.84Min Ren; Song-Song Bao; Rute A. S. Ferreira; Li-Min Zheng; Luis D. Carlos
A layered erbium phosphonate in pseudo-D5h symmetry exhibiting field-tunable magnetic relaxation and optical correlation
Chem.Commun., 2014, 50, 7621
7114653 CIFC9 H30 Cl N3 O17 P3 YP -19.133; 9.226; 15.198
88.281; 76.324; 75.787
1205.7Min Ren; Song-Song Bao; Rute A. S. Ferreira; Li-Min Zheng; Luis D. Carlos
A layered erbium phosphonate in pseudo-D5h symmetry exhibiting field-tunable magnetic relaxation and optical correlation
Chem.Commun., 2014, 50, 7621
7114654 CIFC21 H24 B2 F8 Fe N12 O3P 3 1 c12.6729; 12.6729; 10.9338
90; 90; 120
1520.74Jonathan J. Loughrey; Tim P. Comyn; David C. Apperley; Marc A. Little; Malcolm A. Halcrow
Complex thermal expansion properties in a molecular honeycomb lattice
Chem.Commun., 2014, 50, 7601
7114655 CIFC21 H24 B2 F8 Fe N12 O3P 3 1 c12.6653; 12.6653; 11.0258
90; 90; 120
1531.7Jonathan J. Loughrey; Tim P. Comyn; David C. Apperley; Marc A. Little; Malcolm A. Halcrow
Complex thermal expansion properties in a molecular honeycomb lattice
Chem.Commun., 2014, 50, 7601
7114656 CIFC21 H24 B2 F8 Fe N12 O3P 3 1 c12.6778; 12.6778; 10.9308
90; 90; 120
1521.49Jonathan J. Loughrey; Tim P. Comyn; David C. Apperley; Marc A. Little; Malcolm A. Halcrow
Complex thermal expansion properties in a molecular honeycomb lattice
Chem.Commun., 2014, 50, 7601
7114657 CIFC21 H24 B2 F8 Fe N12 O3P 3 1 c12.66; 12.66; 10.9359
90; 90; 120
1517.9Jonathan J. Loughrey; Tim P. Comyn; David C. Apperley; Marc A. Little; Malcolm A. Halcrow
Complex thermal expansion properties in a molecular honeycomb lattice
Chem.Commun., 2014, 50, 7601
7114658 CIFC53 H34 F12 Fe O7 P2 Ru3 SP 21 21 2110.9799; 14.7027; 35.1126
90; 90; 90
5668.4Ahmed F. Abdel-Magied; Amrendra K. Singh; Matti Haukka; Michael G. Richmond; Ebbe Nordlander
Diastereomeric control of enantioselectivity: evidence for metal cluster catalysis
Chem.Commun., 2014, 50, 7705
7114659 CIFC53 H34 F12 Fe O7 P2 Ru3 SP 21 21 2111.9655; 20.1151; 49.045
90; 90; 90
11804.5Ahmed F. Abdel-Magied; Amrendra K. Singh; Matti Haukka; Michael G. Richmond; Ebbe Nordlander
Diastereomeric control of enantioselectivity: evidence for metal cluster catalysis
Chem.Commun., 2014, 50, 7705
7114660 CIFC28 H30 B2 N4 O2P 1 21/c 111.8021; 11.1964; 10.108
90; 115.025; 90
1210.29Aneliia Shchyrba; Susanne C. Martens; Christian Wackerlin; Manfred Matena; Toni Ivas; Hubert Wadepohl; Meike Stohr; Thomas A. Jung; Lutz H. Gade
Covalent assembly of a two-dimensional molecular 'sponge' on a Cu(111) surface: confined electronic surface states in open and closed pores
Chem.Commun., 2014, 50, 7628
7114661 CIFC26 H62 O5 P2 Si3 SrP b c a14.051; 16.095; 33.152
90; 90; 90
7497Kirsten Reuter; Carsten von Hanisch
Stepwise synthesis of a stable diphosphasilirane and its unexpected dimerization
Chem.Commun., 2014, 50, 7709
7114662 CIFC34 H82 Ba O9 P2 Si3P 21 21 2112.266; 16.57; 23.821
90; 90; 90
4841.6Kirsten Reuter; Carsten von Hanisch
Stepwise synthesis of a stable diphosphasilirane and its unexpected dimerization
Chem.Commun., 2014, 50, 7709
7114663 CIFC36 H84 O2 P4 Si6P 1 21/n 113.6209; 25.4353; 14.457
90; 101.199; 90
4913.3Kirsten Reuter; Carsten von Hanisch
Stepwise synthesis of a stable diphosphasilirane and its unexpected dimerization
Chem.Commun., 2014, 50, 7709
7114665 CIFC90 H103 F12 N3 O16 P2P 1 21/n 112.115; 34.605; 20.873
90; 100.404; 90
8607Fei Zeng; Zheng Meng; Ying Han; Chuan-Feng Chen
Formation of a 'pseudosuitane'-type complex between a triptycene-derived bis(crown ether) host and 1,1'-(anthracene-9,10-diyl)bis(N-benzylmethanaminium): a new method for the synthesis of linear polyrotaxanes
Chem.Commun., 2014, 50, 7611
7115262 CIFC84 H144 Eu4 Mn8 N12 O116P 1 21/n 18.98163; 24.4814; 17.3224
90; 99.3878; 90
3757.89Zheng Niu; Sheng Fang; Jian-Gong Ma; Xiao-Ping Zhang; Peng Cheng
Enhancement of adsorption selectivity for MOFs under mild activation and regeneration conditions
Chem.Commun., 2014, 50, 7797
7115263 CIFC86.67 H104 Eu4 Mn8 N12 O93.33P 1 21/n 19.019; 24.563; 17.339
90; 99.422; 90
3789.4Zheng Niu; Sheng Fang; Jian-Gong Ma; Xiao-Ping Zhang; Peng Cheng
Enhancement of adsorption selectivity for MOFs under mild activation and regeneration conditions
Chem.Commun., 2014, 50, 7797
7115264 CIFC95 H126.65 Eu4 Mn8 N12 O97.33P 1 21/n 18.9103; 24.1109; 17.3062
90; 98.343; 90
3678.6Zheng Niu; Sheng Fang; Jian-Gong Ma; Xiao-Ping Zhang; Peng Cheng
Enhancement of adsorption selectivity for MOFs under mild activation and regeneration conditions
Chem.Commun., 2014, 50, 7797
7115265 CIFC44 H49 F6 N5 O SP 1 21 115.683; 16.311; 17.436
90; 110.279; 90
4183.8Matea Vlatkovic; Luca Bernardi; Edwin Otten; Ben L. Feringa
Dual stereocontrol over the Henry reaction using a light- and heat-triggered organocatalyst
Chem.Commun., 2014, 50, 7773
7115266 CIFC46 H34 Cd2 N12 O11P -110.2812; 13.6284; 16.875
85.265; 75.138; 81.491
2257.75Biswajit Bhattacharya; Animesh Layek; Md. Mehboob Alam; Dilip Kumar Maity; Swapan Chakrabarti; Partha Pratim Ray; Debajyoti Ghoshal
Cd(II) based metal-organic framework behaving as a Schottky barrier diode
Chem.Commun., 2014, 50, 7858
7115267 CIFC24 H16 B2 N2 OP 21 21 215.2893; 15.6927; 20.2458
90; 90; 90
1680.47Matthias Muller; Stefan Behnle; Cacilia Maichle-Mossmer; Holger F. Bettinger
Boron-nitrogen substituted perylene obtained through photocyclisation
Chem.Commun., 2014, 50, 7821
7115268 CIFC30 H40 Br2 Cl Fe N2 O2P 21 21 219.9311; 14.3912; 22.008
90; 90; 90
3145.4Xin Gu; Yan Zhang; Zhen-Jiang Xu; Chi-Ming Che
Iron(III)-salan complexes catalysed highly enantioselective fluorination and hydroxylation of beta-keto esters and N-Boc oxindoles
Chem.Commun., 2014, 50, 7870
7115269 CIFC16 H12 Br NP 21 21 214.08853; 11.1945; 27.8189
90; 90; 90
1273.24Masashi Shibata; Kazunari Nakajima; Yoshiaki Nishibayashi
Enantioselective intramolecular propargylic amination using chiral copper-pybox complexes as catalysts
Chem.Commun., 2014, 50, 7874
7115270 CIFC11 H10 Br2 O3P b c a10.6547; 14.1169; 16.878
90; 90; 90
2538.6Tian-Yang Yu; Yao Wang; Xiu-Qin Hu; Peng-Fei Xu
Triphenylphosphine oxide-catalyzed stereoselective poly- and dibromination of unsaturated compounds
Chem.Commun., 2014, 50, 7817
7115271 CIFC73 H69 Mn4 N13P 1 21/c 113.6312; 18.1096; 27.002
90; 93.5179; 90
6653Michael R. Gau; Clifton R. Hamilton; Michael J. Zdilla
Preparation of a 'twisted basket'Mn4N8 cluster: a two-hydrogen-atom reduced analogue of the Mn4N8 pinned butterfly
Chem.Commun., 2014, 50, 7780
7115272 CIFC72 H72 Cl8 Mn4 N12I 41/a c d18.311; 18.311; 47.15
90; 90; 90
15809Michael R. Gau; Clifton R. Hamilton; Michael J. Zdilla
Preparation of a 'twisted basket'Mn4N8 cluster: a two-hydrogen-atom reduced analogue of the Mn4N8 pinned butterfly
Chem.Commun., 2014, 50, 7780
7115273 CIFC88 H84 Mn4 N16F d d 218.1979; 22.599; 40.496
90; 90; 90
16654Michael R. Gau; Clifton R. Hamilton; Michael J. Zdilla
Preparation of a 'twisted basket'Mn4N8 cluster: a two-hydrogen-atom reduced analogue of the Mn4N8 pinned butterfly
Chem.Commun., 2014, 50, 7780
7115274 CIFC14 H14 Fe I N O4P -16.997; 7.231; 15.311
93.523; 97.073; 101.321
750.9Midori Akiyama; Kengo Akagawa; Hidetake Seino; Kazuaki Kudo
Peptide-catalyzed kinetic resolution of planar-chiral metallocenes
Chem.Commun., 2014, 50, 7893
7115275 CIFC28 H24 O4C 1 2/c 117.9087; 13.6467; 17.9157
90; 94.4847; 90
4365.1Stuart Aiken; Kathryn Booth; Christopher D. Gabbutt; B. Mark Heron; Craig R. Rice; Azzam Charaf-Eddin; Denis Jacquemin
The first structural and spectroscopic characterisation of a ring-opened form of a 2H-naphtho[1,2-b]pyran: a novel photomerocyanine
Chem.Commun., 2014, 50, 7900
7115276 CIFC39.5 H70 B N3C 1 2/c 127.415; 18.243; 17.305
90; 114.471; 90
7877David A. Ruiz; Mohand Melaimi; Guy Bertrand
An efficient synthetic route to stable bis(carbene)borylenes [(L1)(L2)BH]
Chem.Commun., 2014, 50, 7837
7115277 CIFC35 H54 B N3P 1 21/n 116.2182; 9.3515; 21.6436
90; 104.492; 90
3178.1David A. Ruiz; Mohand Melaimi; Guy Bertrand
An efficient synthetic route to stable bis(carbene)borylenes [(L1)(L2)BH]
Chem.Commun., 2014, 50, 7837
7115278 CIFC62 H84 B2 F3 N3 O3 SP 1 21/c 122.26; 13.788; 19.769
90; 106.57; 90
5816David A. Ruiz; Mohand Melaimi; Guy Bertrand
An efficient synthetic route to stable bis(carbene)borylenes [(L1)(L2)BH]
Chem.Commun., 2014, 50, 7837
7115279 CIFC60 H74 B2 F3 N3 O3 SP 1 21/c 114.2524; 13.4771; 28.1965
90; 91.722; 90
5413.6David A. Ruiz; Mohand Melaimi; Guy Bertrand
An efficient synthetic route to stable bis(carbene)borylenes [(L1)(L2)BH]
Chem.Commun., 2014, 50, 7837
7115280 CIFC23 H37 B F3 N O3 SP 1 21/n 111.1389; 13.5546; 16.2662
90; 95.456; 90
2444.8David A. Ruiz; Mohand Melaimi; Guy Bertrand
An efficient synthetic route to stable bis(carbene)borylenes [(L1)(L2)BH]
Chem.Commun., 2014, 50, 7837
7115281 CIFC50 H111 Co N3 O14 V4P 1 21 111.853; 21.6446; 12.5652
90; 93.647; 90
3217.1Andrey Seliverstov; Johannes Forster; Magdalena Heiland; Johannes Unfried; Carsten Streb
The anion-binding polyanion: a molecular cobalt vanadium oxide with anion-sensitive visual response
Chem.Commun., 2014, 50, 7840
7115282 CIFC55 H113 Co N3 O14 V4C 1 c 124.15; 23.6855; 23.9678
90; 93.9267; 90
13677.5Andrey Seliverstov; Johannes Forster; Magdalena Heiland; Johannes Unfried; Carsten Streb
The anion-binding polyanion: a molecular cobalt vanadium oxide with anion-sensitive visual response
Chem.Commun., 2014, 50, 7840
7115284 CIFC37 H45 Na O3P -110.364; 18.028; 33.59
90.01; 90.01; 93.4
6265Jan Klett
Monometalated tribenzotriquinacene: exo and endo coordination of sodium and potassium with a rigid bowl-shaped hydrocarbon anion
Chem.Commun., 2014, 50, 7929
7115285 CIFC37 H45 K O3C 1 c 116.783; 12.416; 15.368
90; 102.75; 90
3123.4Jan Klett
Monometalated tribenzotriquinacene: exo and endo coordination of sodium and potassium with a rigid bowl-shaped hydrocarbon anion
Chem.Commun., 2014, 50, 7929
7115288 CIFC20 H30 Cl4 F6 N4 O6 S2 SiP -18.1122; 11.4867; 18.796
95.057; 98.939; 108.631
1621.66Alasdair P. M. Robertson; Jordan N. Friedmann; Hilary A. Jenkins; Neil Burford
Exploring structural trends for complexes of Me2E(OSO2CF3)2 (E = Si, Ge, Sn) with pyridine derivatives
Chem.Commun., 2014, 50, 7979
7115289 CIFC14 H14 F6 N2 O6 S2 SiC 1 c 114.1596; 22.794; 7.3679
90; 118.801; 90
2083.9Alasdair P. M. Robertson; Jordan N. Friedmann; Hilary A. Jenkins; Neil Burford
Exploring structural trends for complexes of Me2E(OSO2CF3)2 (E = Si, Ge, Sn) with pyridine derivatives
Chem.Commun., 2014, 50, 7979
7115290 CIFC20 H26 F6 Ge N5 O6 S2P 1 21/c 110.6701; 11.5348; 23.336
90; 93.922; 90
2865.4Alasdair P. M. Robertson; Jordan N. Friedmann; Hilary A. Jenkins; Neil Burford
Exploring structural trends for complexes of Me2E(OSO2CF3)2 (E = Si, Ge, Sn) with pyridine derivatives
Chem.Commun., 2014, 50, 7979
7115291 CIFC14 H14 F6 Ge N2 O6 S2P -17.7487; 11.1678; 12.422
110.419; 95.688; 95.436
992.76Alasdair P. M. Robertson; Jordan N. Friedmann; Hilary A. Jenkins; Neil Burford
Exploring structural trends for complexes of Me2E(OSO2CF3)2 (E = Si, Ge, Sn) with pyridine derivatives
Chem.Commun., 2014, 50, 7979
7115292 CIFC18 H26 F6 N4 O6 S2 SnC 1 2/c 19.4758; 13.6913; 21.1332
90; 100.452; 90
2696.2Alasdair P. M. Robertson; Jordan N. Friedmann; Hilary A. Jenkins; Neil Burford
Exploring structural trends for complexes of Me2E(OSO2CF3)2 (E = Si, Ge, Sn) with pyridine derivatives
Chem.Commun., 2014, 50, 7979
7115293 CIFC14 H14 F6 N2 O6 S2 SnP 1 21/c 110.623; 15.281; 13.418
90; 113.235; 90
2001.5Alasdair P. M. Robertson; Jordan N. Friedmann; Hilary A. Jenkins; Neil Burford
Exploring structural trends for complexes of Me2E(OSO2CF3)2 (E = Si, Ge, Sn) with pyridine derivatives
Chem.Commun., 2014, 50, 7979

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 19 | Next 100 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

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