Crystallography Open Database
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Result: there are 1859 entries in the selection
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Searching journal of publication like 'Chem. Commun.' volume of publication is 50
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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7116032 | CIF | C37 H10 N O4 Rh S2 | P n m a | 15.7899; 19.3598; 15.892 90; 90; 90 | 4858 | Amineh Aghabali; Marilyn M. Olmstead; Alan L. Balch Zipping up fullerenes into polymers using rhodium(II) acetate dimer and N(CH2CH2)2NC60 as building blocks Chem.Commun., 2014, 50, 15152 |
7116033 | CIF | C143 H20 N2 O8 Rh2 S2 | P m m a | 19.6991; 15.8057; 12.8041 90; 90; 90 | 3986.7 | Amineh Aghabali; Marilyn M. Olmstead; Alan L. Balch Zipping up fullerenes into polymers using rhodium(II) acetate dimer and N(CH2CH2)2NC60 as building blocks Chem.Commun., 2014, 50, 15152 |
7116034 | CIF | C20 H24 I N2 Rh | P 1 21/c 1 | 14.1979; 8.3992; 16.4769 90; 102.84; 90 | 1915.8 | Debasish Ghorai; Joyanta Choudhury Exploring a unique reactivity of N-heterocyclic carbenes (NHC) in rhodium(III)-catalyzed intermolecular C-H activation/annulation Chem.Commun., 2014, 50, 15159 |
7116035 | CIF | C25 H19 F3 N2 O3 S | C 1 2/c 1 | 16.032; 8.837; 31.193 90; 103.528; 90 | 4297 | Debasish Ghorai; Joyanta Choudhury Exploring a unique reactivity of N-heterocyclic carbenes (NHC) in rhodium(III)-catalyzed intermolecular C-H activation/annulation Chem.Commun., 2014, 50, 15159 |
7116036 | CIF | C24 H19 F6 N2 P | P b c a | 9.6965; 14.8468; 30.235 90; 90; 90 | 4352.7 | Debasish Ghorai; Joyanta Choudhury Exploring a unique reactivity of N-heterocyclic carbenes (NHC) in rhodium(III)-catalyzed intermolecular C-H activation/annulation Chem.Commun., 2014, 50, 15159 |
7116037 | CIF | C29 H21 F3 N2 O3 S | P -1 | 8.7315; 9.0652; 16.3291 83.644; 88.973; 71.5 | 1217.97 | Debasish Ghorai; Joyanta Choudhury Exploring a unique reactivity of N-heterocyclic carbenes (NHC) in rhodium(III)-catalyzed intermolecular C-H activation/annulation Chem.Commun., 2014, 50, 15159 |
7116038 | CIF | C25 H21 F3 N2 O3 S | P b c a | 18.9839; 10.2711; 22.667 90; 90; 90 | 4419.7 | Debasish Ghorai; Joyanta Choudhury Exploring a unique reactivity of N-heterocyclic carbenes (NHC) in rhodium(III)-catalyzed intermolecular C-H activation/annulation Chem.Commun., 2014, 50, 15159 |
7116039 | CIF | C27 H19 F3 N2 O3 S | P 1 21/c 1 | 14.0991; 7.9225; 21.8819 90; 100.609; 90 | 2402.4 | Debasish Ghorai; Joyanta Choudhury Exploring a unique reactivity of N-heterocyclic carbenes (NHC) in rhodium(III)-catalyzed intermolecular C-H activation/annulation Chem.Commun., 2014, 50, 15159 |
7116040 | CIF | C16 H20 N4 Ni2 O4 | P 1 21/c 1 | 11.0898; 12.8028; 14.4904 90; 120.131; 90 | 1779.36 | Hassib Audi; Zhongrui Chen; Azzam Charaf-Eddin; Anthony D'Aleo; Gabriel Canard; Denis Jacquemin; Olivier Siri Extendable nickel complex tapes that reach NIR absorptions Chem.Commun., 2014, 50, 15140 |
7116041 | CIF | C36 H24 Cu6 I6 In3 N6 O16 | P 6/m c c | 21.9173; 21.9173; 28.2685 90; 90; 120 | 11760 | Jinjie Qian; Feilong Jiang; Kongzhao Su; Jie Pan; Zhenzhen Xue; Linfeng Liang; Partha Pratim Bag; Maochun Hong Heterometallic cluster-based indium-organic frameworks Chem.Commun., 2014, 50, 15224 |
7116042 | CIF | C21 H18 O3 | P 1 21/c 1 | 9.8452; 16.351; 10.564 90; 103.618; 90 | 1652.8 | Mieko Arisawa; Saori Tanii; Masahiko Yamaguchi A palladium-catalyzed addition reaction of aroyl/heteroaroyl acid anhydrides to norbornenes Chem.Commun., 2014, 50, 15267 |
7116043 | CIF | C30 H46 N4 O6 | P b c a | 9.4439; 11.2685; 28.3698 90; 90; 90 | 3019.1 | Can Xue; Chunling Fu; Shengming Ma Highly regio- and stereoselective nitro-oxoamination of mono-substituted allenes Chem.Commun., 2014, 50, 15333 |
7116044 | CIF | C18 H25 Br N2 O3 | P b c n | 18.9268; 8.3654; 23.4009 90; 90; 90 | 3705.1 | Can Xue; Chunling Fu; Shengming Ma Highly regio- and stereoselective nitro-oxoamination of mono-substituted allenes Chem.Commun., 2014, 50, 15333 |
7116045 | CIF | Al6 H10 Na2 O30 P6 | P c a 21 | 17.495; 10.321; 13.577 90; 90; 90 | 2451.5 | Yanyan Wang; Yanjun Sun; Ying Mu; Chuanqi Zhang; Jiyang Li; Jihong Yu Organotemplate-free hydrothermal synthesis of an aluminophosphate molecular sieve with AEN zeotype topology and properties of its derivatives Chem.Commun., 2014, 50, 15400 |
7116046 | CIF | C15 H16 N2 O3 S | P c c n | 18.8609; 9.2843; 16.5808 90; 90; 90 | 2903.5 | Qian Zhang; Xu Liu; Xiaoqing Xin; Rui Zhang; Yongjiu Liang; Dewen Dong Formal [4+2] annulation of enaminones and cyanomethyl sulfur ylide: one:pot access to polysubstituted pyridin-2(1H)-ones Chem.Commun., 2014, 50, 15378 |
7116047 | CIF | C15 H13 Cl2 N3 Pd | P 1 21/m 1 | 10.122; 6.909; 10.959 90; 103.632; 90 | 744.8 | Arturo Juzgado; M. Mercedes Lorenzo-Garcia; Myriam Barrejon; Ana M. Rodriguez; Julian Rodriguez-Lopez; Sonia Merino; Juan Tejeda Chelation assistance as a tool for the selective preparation of an imidazole-based mesoionic palladium carbene complex Chem.Commun., 2014, 50, 15313 |
7116048 | CIF | C16 H16 Ag N3 O3 S | C 1 2/c 1 | 20.793; 11.193; 14.632 90; 92.944; 90 | 3400.9 | Arturo Juzgado; M. Mercedes Lorenzo-Garcia; Myriam Barrejon; Ana M. Rodriguez; Julian Rodriguez-Lopez; Sonia Merino; Juan Tejeda Chelation assistance as a tool for the selective preparation of an imidazole-based mesoionic palladium carbene complex Chem.Commun., 2014, 50, 15313 |
7116049 | CIF | C27 H24 Br N O3 | P 21 21 21 | 10.518; 10.893; 19.602 90; 90; 90 | 2245.9 | Min Wang; Zi-Qiang Rong; Yu Zhao Stereoselective synthesis of epsilon-lactones or spiro-heterocycles through NHC-catalyzed annulation: divergent reactivity by catalyst control Chem.Commun., 2014, 50, 15309 |
7116050 | CIF | C27 H29 Cl O3 | P b c a | 8.31; 8.664; 65.12 90; 90; 90 | 4688 | Veejendra K. Yadav; Ashish K. Verma; Piyush Kumar; Vijaykumar Hulikal 2-Arylcyclopropylmethanol as a substitute for homoallyl aryl alcohol in the construction of cis-2,6-disubstituted tetrahydropyran: synthesis of (+/-)-centrolobine Chem.Commun., 2014, 50, 15457 |
7116051 | CIF | C10 H24 Ge N2 Si | P 1 21/n 1 | 11.4041; 6.2297; 20.3921 90; 102.231; 90 | 1415.85 | P. Steiniger; G. Bendt; D. Blaser; C. Wolper; S. Schulz Germane vs. digermane formation Chem.Commun., 2014, 50, 15461 |
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