Crystallography Open Database
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Searching journal of publication like 'Chemical Communications' volume of publication is 52
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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7118218 | CIF | C36 H26 Br2 O4 | P 21 21 21 | 5.6288; 12.578; 41.669 90; 90; 90 | 2950.1 | Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation. Chemical communications (Cambridge, England), 2015, 52, 788-791 |
7118219 | CIF | C36 H28 O4 | P 21 21 21 | 9.263; 12.8186; 22.369 90; 90; 90 | 2656.1 | Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation. Chemical communications (Cambridge, England), 2015, 52, 788-791 |
7118220 | CIF | C36 H26 Br2 O4 | P 21 21 21 | 5.5911; 13.004; 40.623 90; 90; 90 | 2953.6 | Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation. Chemical communications (Cambridge, England), 2015, 52, 788-791 |
7118221 | CIF | C13 H11 F N2 | P -1 | 10.0641; 11.0425; 12.1824 114.924; 95.055; 111.476 | 1094.39 | Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak 'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks. Chemical communications (Cambridge, England), 2016, 52, 2141-2144 |
7118222 | CIF | C13 H10 F2 N2 | P 1 21/c 1 | 12.7028; 8.3775; 11.5509 90; 117.017; 90 | 1095.1 | Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak 'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks. Chemical communications (Cambridge, England), 2016, 52, 2141-2144 |
7118223 | CIF | C41 H33 N3 O6 | P 1 21/c 1 | 11.1829; 11.5006; 26.2259 90; 92.219; 90 | 3370.4 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
7118224 | CIF | C41 H33 Cd Cl0 I2 N3 O6 | R -3 :H | 54.6374; 54.6374; 8.9458 90; 90; 120 | 23127.6 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
7118225 | CIF | C42.17 H36 Br Cd I2 N3 O6.33 | R -3 :H | 54.5811; 54.5811; 8.9081 90; 90; 120 | 22982.7 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
7118226 | CIF | C42 H35 Cd I4 N3 O6 | R -3 :H | 54.772; 54.772; 8.8733 90; 90; 120 | 23053.3 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
7118227 | CIF | C41 H33 Cd I2 N3 O6 | R -3 :H | 54.8819; 54.8819; 8.8759 90; 90; 120 | 23152.7 | Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation. Chemical communications (Cambridge, England), 2016, 52, 2545-2548 |
7118230 | CIF | C26 H18 Br Cl4 N2 O4 | P 1 21 1 | 13.0622; 8.2259; 13.1485 90; 106.33; 90 | 1355.79 | Cao, Zhong-Yan; Zhao, Yu-Lei; Zhou, Jian Sequential Au(i)/chiral tertiary amine catalysis: a tandem C-H functionalization of anisoles or a thiophene/asymmetric Michael addition sequence to quaternary oxindoles. Chemical communications (Cambridge, England), 2016, 52, 2537-2540 |
7118231 | CIF | C27 H21 Br Cl2 N2 O5 | P 21 21 21 | 12.315; 13.9146; 15.2049 90; 90; 90 | 2605.49 | Cao, Zhong-Yan; Zhao, Yu-Lei; Zhou, Jian Sequential Au(i)/chiral tertiary amine catalysis: a tandem C-H functionalization of anisoles or a thiophene/asymmetric Michael addition sequence to quaternary oxindoles. Chemical communications (Cambridge, England), 2016, 52, 2537-2540 |
7118232 | CIF | C31 H30 Br N3 O5 | I 1 2 1 | 14.6406; 9.57209; 19.5953 90; 97.003; 90 | 2725.62 | Zhao, Kun; Zhi, Ying; Li, Xinyi; Puttreddy, Rakesh; Rissanen, Kari; Enders, Dieter Asymmetric synthesis of 3,3'-pyrrolidinyl-dispirooxindoles via a one-pot organocatalytic Mannich/deprotection/aza-Michael sequence. Chemical communications (Cambridge, England), 2016, 52, 2249-2252 |
7118241 | CIF | C40 H24 In N2 O8 | C 1 2/c 1 | 28.286; 20.9422; 27.5862 90; 120.798; 90 | 14037 | Li, Xingjun; Chen, Xueyuan; Jiang, Feilong; Chen, Lian; Lu, Shan; Chen, Qihui; Wu, Mingyan; Yuan, Daqiang; Hong, Maochun The dynamic response of a flexible indium based metal-organic framework to gas sorption. Chemical communications (Cambridge, England), 2016, 52, 2277-2280 |
7118242 | CIF | C40 H24 In N2 O8 | I 1 2/c 1 | 26.9793; 21.3293; 26.4721 90; 97.001; 90 | 15119.8 | Li, Xingjun; Chen, Xueyuan; Jiang, Feilong; Chen, Lian; Lu, Shan; Chen, Qihui; Wu, Mingyan; Yuan, Daqiang; Hong, Maochun The dynamic response of a flexible indium based metal-organic framework to gas sorption. Chemical communications (Cambridge, England), 2016, 52, 2277-2280 |
7118243 | CIF | C25 H32 B F6 I2 N8 O P W | P 1 21/n 1 | 8.352; 22.5729; 18.2914 90; 100.772; 90 | 3387.69 | Helmdach, Kai; Rüger, Julia; Villinger, Alexander; Seidel, Wolfram W. Dual nucleophilic substitution at a W(ii) η(2)-coordinated diiodo acetylene leading to an amidinium carbyne complex. Chemical communications (Cambridge, England), 2016, 52, 2616-2619 |
7118244 | CIF | C33 H38 B F6 N8 O2 P W | P 1 21/n 1 | 25.7178; 11.6201; 25.7435 90; 97.686; 90 | 7624.2 | Helmdach, Kai; Rüger, Julia; Villinger, Alexander; Seidel, Wolfram W. Dual nucleophilic substitution at a W(ii) η(2)-coordinated diiodo acetylene leading to an amidinium carbyne complex. Chemical communications (Cambridge, England), 2016, 52, 2616-2619 |
7118245 | CIF | C20 H21 Br O5 | P 1 21/c 1 | 12.3928; 8.3243; 18.5364 90; 95.888; 90 | 1902.15 | Yu, Zhunzhun; Qiu, Haile; Liu, Lu; Zhang, Junliang Gold-catalyzed construction of two adjacent quaternary stereocenters via sequential C-H functionalization and aldol annulation. Chemical communications (Cambridge, England), 2016, 52, 2257-2260 |
7118246 | CIF | C21 H23 Br O5 | P 1 21/c 1 | 9.2166; 9.0685; 23.2491 90; 99.08; 90 | 1918.83 | Yu, Zhunzhun; Qiu, Haile; Liu, Lu; Zhang, Junliang Gold-catalyzed construction of two adjacent quaternary stereocenters via sequential C-H functionalization and aldol annulation. Chemical communications (Cambridge, England), 2016, 52, 2257-2260 |
7118247 | CIF | C27 H24 N2 O3 | P -1 | 10.9476; 11.03; 11.0714 86.1003; 64.8281; 60.6087 | 1037.28 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118249 | CIF | C31 H24 N2 O2 | P -1 | 9.365; 11.4265; 11.9971 74.104; 80.112; 71.016 | 1162.72 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118250 | CIF | C25 H20 N3 O | P 1 21/c 1 | 18.817; 10.53; 9.5207 90; 96.996; 90 | 1872.4 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118251 | CIF | C28 H28 Cl N O3 | P -1 | 9.469; 10.0316; 13.1967 83.975; 70.468; 85.668 | 1173.8 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118252 | CIF | C19 H15 N O4 | P 1 21/c 1 | 8.3566; 17.7311; 10.5304 90; 101.637; 90 | 1528.24 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118253 | CIF | C27 H26 N2 O3 | P -1 | 8.2128; 12.0722; 12.1473 80.826; 73.356; 74.316 | 1106.54 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118254 | CIF | C18 H19 N O3 | P n m a | 15.9415; 14.8517; 6.2573 90; 90; 90 | 1481.5 | Zhu, Xu; Chiba, Shunsuke Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides. Chemical communications (Cambridge, England), 2016, 52, 2473-2476 |
7118255 | CIF | C14 H15 N O5 | P 1 21/c 1 | 9.5866; 19.5978; 7.6285 90; 111.316; 90 | 1335.17 | Baumann, A. N.; Music, A.; Karaghiosoff, K.; Didier, D. Highly diastereoselective approach to methylenecyclopropanes via boron-homologation/allylboration sequences. Chemical communications (Cambridge, England), 2016, 52, 2529-2532 |
7118256 | CIF | C45 H37 Cl N5 O P Ru | P 1 21/n 1 | 13.9666; 12.6444; 21.018 90; 95.457; 90 | 3694.9 | Tseng, Kuei-Nin T; Lin, Steve; Kampf, Jeff W.; Szymczak, Nathaniel K. Upgrading ethanol to 1-butanol with a homogeneous air-stable ruthenium catalyst. Chemical communications (Cambridge, England), 2016, 52, 2901-2904 |
7118257 | CIF | C39 H31 Cl N5 O3 P Ru | P 1 21/c 1 | 16.1333; 12.495; 16.9891 90; 98.709; 90 | 3385.27 | Tseng, Kuei-Nin T; Lin, Steve; Kampf, Jeff W.; Szymczak, Nathaniel K. Upgrading ethanol to 1-butanol with a homogeneous air-stable ruthenium catalyst. Chemical communications (Cambridge, England), 2016, 52, 2901-2904 |
7118258 | CIF | C38 H42 Cl6 Cu2 N6 | P -1 | 8.2153; 11.1662; 11.5343 85.272; 84.43; 77.543 | 1026.24 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118259 | CIF | C38 H42 Cl6 Cu2 N6 | P -1 | 8.1887; 10.9691; 11.3579 85.0163; 85.1738; 77.5551 | 990.21 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118260 | CIF | C40 H46 Cl6 Cu2 N6 | P -1 | 8.3056; 11.1055; 11.873 86.315; 89.284; 77.72 | 1067.9 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118261 | CIF | C40 H46 Cl6 Cu2 N6 | P -1 | 8.3293; 10.9929; 11.7343 86.079; 89.732; 77.869 | 1047.9 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118262 | CIF | C38 H40 Cl8 Cu2 N6 | P -1 | 8.253; 10.948; 11.802 85.792; 89.721; 78.477 | 1042 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118263 | CIF | C40 H46 Cl6 Cu2 N6 O2 | P -1 | 8.292; 10.995; 12.277 84.743; 86.68; 78.394 | 1090.9 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118264 | CIF | C18 H18 Cl Cu N4 O2 | P 21 21 21 | 9.0636; 9.6375; 20.925 90; 90; 90 | 1827.8 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118265 | CIF | C21 H25 Cl Cu N3 | P 1 21/c 1 | 9.5545; 8.8034; 23.9329 90; 96.6239; 90 | 1999.61 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118266 | CIF | C36 H38 Cl2 Cu2 N6 | P 1 21/n 1 | 10.0169; 15.969; 10.7209 90; 95.056; 90 | 1708.24 | Nitsch, Jörn; Lacemon, Frederick; Lorbach, Andreas; Eichhorn, Antonius; Cisnetti, Federico; Steffen, Andreas Cuprophilic interactions in highly luminescent dicopper(i)-NHC-picolyl complexes - fast phosphorescence or TADF? Chemical communications (Cambridge, England), 2016, 52, 2932-2935 |
7118267 | CIF | C43.5 H37 Al Au Cl F36 N2 O4 P4 | P 1 21/n 1 | 10.7137; 38.3822; 14.7478 90; 90.909; 90 | 6063.8 | Borger, Jaap E.; Bakker, Martijn S.; Ehlers, Andreas W.; Lutz, Martin; Chris Slootweg, J.; Lammertsma, Koop Functionalization of P4 in the coordination sphere of coinage metal cations. Chemical communications (Cambridge, England), 2016, 52, 3284-3287 |
7118268 | CIF | C94 H97 Al Au2 F36 N4 O4 P4 | C 1 2/c 1 | 39.9091; 25.1072; 22.5843 90; 100.38; 90 | 22259.3 | Borger, Jaap E.; Bakker, Martijn S.; Ehlers, Andreas W.; Lutz, Martin; Chris Slootweg, J.; Lammertsma, Koop Functionalization of P4 in the coordination sphere of coinage metal cations. Chemical communications (Cambridge, England), 2016, 52, 3284-3287 |
7118269 | CIF | C27 H24 Br N O3 | P 21 21 21 | 8.8669; 14.7074; 17.9059 90; 90; 90 | 2335.1 | Li, Mingfeng; Guo, Xin; Jin, Weifeng; Zheng, Qing; Liu, Shunying; Hu, Wenhao An enantioselective three-component reaction of diazoacetates with indoles and enals by iridium/iminium co-catalysis. Chemical communications (Cambridge, England), 2016, 52, 2736-2739 |
7118270 | CIF | C18 H32 O3 Si | C 1 2/c 1 | 29.017; 11.4978; 12.6967 90; 111.472; 90 | 3942 | Stepherson, Jacob R.; Fronczek, Frank R.; Kartika, Rendy An expedient synthesis of functionalized 1,4-diketone-derived compounds via silyloxyallyl cation intermediates. Chemical communications (Cambridge, England), 2016, 52, 2300-2303 |
7118271 | CIF | C52 H44 N2 O20 Zn3 | P -1 | 9.4533; 18.614; 19.976 68.27; 82.61; 82.18 | 3223.2 | Chakraborty, Anindita; Bhattacharyya, Sohini; Hazra, Arpan; Ghosh, Ashta Chandra; Maji, Tapas Kumar Post-synthetic metalation in an anionic MOF for efficient catalytic activity and removal of heavy metal ions from aqueous solution. Chemical communications (Cambridge, England), 2016, 52, 2831-2834 |
7118272 | CIF | C15 H26 Cl N W | P n a 21 | 13.1669; 12.7572; 20.0394 90; 90; 90 | 3366.07 | Wright, Christopher M. R.; Turner, Zoë R; Buffet, Jean-Charles; O'Hare, Dermot Tungsten imido catalysts for selective ethylene dimerisation. Chemical communications (Cambridge, England), 2016, 52, 2850-2853 |
7118273 | CIF | C16 H25 Cl4 N O W | P -1 | 8.5941; 14.1186; 17.4478 95.806; 98.562; 97.484 | 2059.88 | Wright, Christopher M. R.; Turner, Zoë R; Buffet, Jean-Charles; O'Hare, Dermot Tungsten imido catalysts for selective ethylene dimerisation. Chemical communications (Cambridge, England), 2016, 52, 2850-2853 |
7118274 | CIF | C22 H21 N O4 | P -1 | 11.0068; 18.8343; 19.829 72.08; 89.811; 77.711 | 3813.1 | Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine. Chemical communications (Cambridge, England), 2016, 52, 2177-2180 |
7118275 | CIF | C22 H21 N O4 | P -1 | 9.035; 13.258; 16.686 90.402; 103.495; 105.139 | 1871.2 | Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine. Chemical communications (Cambridge, England), 2016, 52, 2177-2180 |
7118276 | CIF | C24 H27 N O3 | C 1 2/c 1 | 44.225; 11.0988; 15.9916 90; 99.538; 90 | 7740.9 | Xiao, Jun-An; Xia, Peng-Ju; Zhang, Xing-Yu; Chen, Xiao-Qing; Ou, Guang-Chuan; Yang, Hua Amide-assisted intramolecular [3+2] annulation of cyclopropane ring-opening: a facile and diastereoselective access to the tricyclic core of (±)-scandine. Chemical communications (Cambridge, England), 2016, 52, 2177-2180 |
7118277 | CIF | C90 H187 O100 | P 1 21 1 | 15.517; 9.825; 21.953 90; 90.05; 90 | 3346.8 | Rutenberg, R.; Leitus, G.; Fallik, E.; Poverenov, E. Discovery of a non classic host guest complexation mode in a β-cyclodextrin/propionic acid model. Chemical communications (Cambridge, England), 2016, 52, 2565-2568 |
7118278 | CIF | C30 H25 F N2 O3 S | P 1 21 1 | 5.552; 17.133; 13.413 90; 93.446; 90 | 1273.6 | Sun, Xiao-Xue; Zhang, Hong-Hao; Li, Guo-Hao; Meng, Li; Shi, Feng Diastereo- and enantioselective construction of an indole-based 2,3-dihydrobenzofuran scaffold via catalytic asymmetric [3+2] cyclizations of quinone monoimides with 3-vinylindoles. Chemical communications (Cambridge, England), 2016, 52, 2968-2971 |
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