Crystallography Open Database
Search results
Result: there are 1796 entries in the selection
Switch to the old layout of the pageDownload 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 'Chem.Commun.' volume of publication is 51
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
7116559 | CIF | C27 H21 Fe N9 Ni O2 | C 1 2/c 1 | 17.3572; 15.1852; 10.1318 90; 91.117; 90 | 2669.96 | Arun Kumar Bar; Celine Pichon; Nayanmoni Gogoi; Carine Duhayon; S. Ramasesha; Jean-Pascal Sutter Single-ion magnet behaviour of heptacoordinated Fe(II) complexes: on the importance of supramolecular organization Chem.Commun., 2015, 51, 3616 |
7116560 | CIF | C23 H21 Cl2 Fe N5 O2 | P 1 21/c 1 | 8.6132; 13.1321; 22.5986 90; 108.557; 90 | 2423.22 | Arun Kumar Bar; Celine Pichon; Nayanmoni Gogoi; Carine Duhayon; S. Ramasesha; Jean-Pascal Sutter Single-ion magnet behaviour of heptacoordinated Fe(II) complexes: on the importance of supramolecular organization Chem.Commun., 2015, 51, 3616 |
7116561 | CIF | C26 H31 N O5 | P b c n | 29.508; 8.3721; 19.678 90; 90; 90 | 4861.3 | Qiao-Hui Deng; Jia-Rong Chen; Qiang Wei; Quan-Qing Zhao; Liang-Qiu Lu; Wen-Jing Xiao Visible-light-induced photocatalytic oxytrifluoromethylation of N-allylamides for the synthesis of CF3-containing oxazolines and benzoxazines Chem.Commun., 2015, 51, 3537 |
7116570 | CIF | C67 H74 N2 O8 S2 | P -1 | 15.302; 15.3895; 15.4431 71.988; 60.74; 87.419 | 2992.4 | Erik Gabrielsson; Haining Tian; Susanna K. Eriksson; Jiajia Gao; Hong Chen; Fusheng Li; Johan Oscarsson; Junliang Sun; Hakan Rensmo; Lars Kloo; Anders Hagfeldt; Licheng Sun Dipicolinic acid: a strong anchoring group with tunable redox and spectral behavior for stable dye-sensitized solar cells Chem.Commun., 2015, 51, 3858 |
7116572 | CIF | C16 H14.5 Cl2 Co N5.5 O | P -1 | 9.611; 13.18; 15.861 75.031; 76.859; 89.895 | 1886.7 | Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes Chem.Commun., 2015, 51, 3739 |
7116573 | CIF | C16 H14.5 Br2 Co N5.5 O | P -1 | 9.832; 13.304; 15.925 105.24; 103.61; 90.386 | 1948.1 | Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes Chem.Commun., 2015, 51, 3739 |
7116574 | CIF | C15 H13 Cl2 Co N5 S | P -1 | 8.479; 9.071; 13.536 77.03; 80.74; 67.56 | 934.4 | Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes Chem.Commun., 2015, 51, 3739 |
7116575 | CIF | C15 H13 Br2 Co N5 S | P -1 | 8.441; 9.015; 13.725 77.19; 80.64; 68.94 | 946.4 | Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes Chem.Commun., 2015, 51, 3739 |
7116576 | CIF | C26 H34 B4 Mo2 O6 Ru2 | C 1 2/c 1 | 17.5892; 15.9899; 11.2183 90; 102.022; 90 | 3085.94 | Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster Chem.Commun., 2015, 51, 3828 |
7116577 | CIF | C22 H36 B4 Mo2 O2 | P 43 21 2 | 9.0041; 9.0041; 31.3056 90; 90; 90 | 2538.06 | Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster Chem.Commun., 2015, 51, 3828 |
7116578 | CIF | C25 H34 B3 Cl Mo2 O5 W | P 1 21/n 1 | 9.0059; 18.5886; 17.7675 90; 99.389; 90 | 2934.6 | Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster Chem.Commun., 2015, 51, 3828 |
7116579 | CIF | C30 H31 B Mo2 O10 Ru2 | P c c n | 17.2668; 30.7845; 12.5659 90; 90; 90 | 6679.4 | Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster Chem.Commun., 2015, 51, 3828 |
7116580 | CIF | C12 H36 Be N2 Si4 | P 1 21/n 1 | 9.8756; 16.6972; 14.5875 90; 109.492; 90 | 2267.55 | D. Naglav; A. Neumann; D. Blaser; C. Wolper; R. Haack; G. Jansen; S. Schulz Bonding situation in Be[N(SiMe3)2]2 - an experimental and computational study Chem.Commun., 2015, 51, 3889 |
7116581 | CIF | C83 H31 Cl2.5 F6 N6 | P -1 | 10.3923; 18.707; 18.841 61.769; 75.03; 74.372 | 3070.6 | Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly Chem.Commun., 2015, 51, 3801 |
7116582 | CIF | C86 H36 Cl12 F6 N6 O6 | C 1 2/c 1 | 37.189; 25.4108; 19.26 90; 107.552; 90 | 17353.4 | Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly Chem.Commun., 2015, 51, 3801 |
7116583 | CIF | C162 H48 S4 | P -1 | 16.8833; 18.4991; 23.1447 100.718; 96.6104; 91.6599 | 7046 | Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly Chem.Commun., 2015, 51, 3801 |
7116584 | CIF | C74 H35 Cl N6 | P -1 | 10.6327; 14.0819; 19.8579 109.255; 90.5719; 109.406 | 2623.52 | Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly Chem.Commun., 2015, 51, 3801 |
7116585 | CIF | C70 H132 As4 Ge8 K3 N8 O18 V | P -1 | 11.9985; 16.7415; 25.3291 80.709; 88.755; 69.258 | 4692.3 | Stefan Mitzinger; Lies Broeckaert; Werner Massa; Florian Weigend; Stefanie Dehnen [V@Ge8As4]^3-^ and [Nb@Ge8As6]^3-^: encapsulation of electron-poor transition metal atoms Chem.Commun., 2015, 51, 3866 |
7116586 | CIF | C63 H124 As6 Ge8 K3 N8 Nb O18 | P -1 | 16.1475; 16.7769; 18.0373 89.184; 80.452; 79.42 | 4736.1 | Stefan Mitzinger; Lies Broeckaert; Werner Massa; Florian Weigend; Stefanie Dehnen [V@Ge8As4]^3-^ and [Nb@Ge8As6]^3-^: encapsulation of electron-poor transition metal atoms Chem.Commun., 2015, 51, 3866 |
7116587 | CIF | C28 H39 N2 O6 P W | P 1 21/c 1 | 10.9216; 23.5529; 14.5767 90; 126.717; 90 | 3005.7 | Jose Manuel Villalba Franco; Takahiro Sasamori; Gregor Schnakenburg; Arturo Espinosa Ferao; Rainer Streubel Going for strain: synthesis of the first 3-imino-azaphosphiridine complexes and their conversion into oxaphosphirane complex valence isomers Chem.Commun., 2015, 51, 3878 |
7116588 | CIF | C22 H29 N2 O5 P W | P -1 | 10.9909; 11.0605; 12.874 108.084; 95.194; 118.186 | 1257.68 | Jose Manuel Villalba Franco; Takahiro Sasamori; Gregor Schnakenburg; Arturo Espinosa Ferao; Rainer Streubel Going for strain: synthesis of the first 3-imino-azaphosphiridine complexes and their conversion into oxaphosphirane complex valence isomers Chem.Commun., 2015, 51, 3878 |
7116589 | CIF | C22 H31 N2 O6 P W | P 1 21/c 1 | 9.5748; 27.7242; 10.5851 90; 115.34; 90 | 2539.5 | Jose Manuel Villalba Franco; Takahiro Sasamori; Gregor Schnakenburg; Arturo Espinosa Ferao; Rainer Streubel Going for strain: synthesis of the first 3-imino-azaphosphiridine complexes and their conversion into oxaphosphirane complex valence isomers Chem.Commun., 2015, 51, 3878 |
7116590 | CIF | C31 H24 Br N O6 | P 1 21 1 | 9.4993; 18.9341; 15.0393 90; 97.203; 90 | 2683.63 | Haipeng Hu; Yangbin Liu; Jing Guo; Lili Lin; Yali Xu; Xiaohua Liu; Xiaoming Feng Enantioselective synthesis of dihydrocoumarin derivatives by chiral scandium(III)-complex catalyzed inverse-electron-demand hetero-Diels-Alder reaction Chem.Commun., 2015, 51, 3835 |
7116599 | CIF | C24 H20 Cl N4 O8 Ru | P 1 21 1 | 10.0833; 9.8576; 12.7262 90; 95.327; 90 | 1259.48 | Javier J. Concepcion; Diane K. Zhong; David J. Szalda; James T. Muckerman; Etsuko Fujita Mechanism of water oxidation by [Ru(bda)(L)2]: the return of the 'blue dimer' Chem.Commun., 2015, 51, 4105 |
7116600 | CIF | C30 H20 Cl N4 O8 Ru | P 21 21 21 | 7.6696; 11.321; 32.206 90; 90; 90 | 2796.4 | Javier J. Concepcion; Diane K. Zhong; David J. Szalda; James T. Muckerman; Etsuko Fujita Mechanism of water oxidation by [Ru(bda)(L)2]: the return of the 'blue dimer' Chem.Commun., 2015, 51, 4105 |
7116601 | CIF | C36 H50 Eu2 N8 O34 Zn | C 1 2/c 1 | 17.0712; 16.981; 20.3832 90; 108.073; 90 | 5617.3 | Peng-Fei Shi; Huan-Cheng Hu; Zhan-Yun Zhang; Gang Xiong; Bin Zhao Heterometal-organic frameworks as highly sensitive and highly selective luminescent probes to detect I^-^ ions in aqueous solutions Chem.Commun., 2015, 51, 3985 |
7116602 | CIF | C36 H50 N8 O34 Tb2 Zn | C 1 2/c 1 | 17.0778; 16.9284; 20.3385 90; 108.115; 90 | 5588.4 | Peng-Fei Shi; Huan-Cheng Hu; Zhan-Yun Zhang; Gang Xiong; Bin Zhao Heterometal-organic frameworks as highly sensitive and highly selective luminescent probes to detect I^-^ ions in aqueous solutions Chem.Commun., 2015, 51, 3985 |
7116603 | CIF | C36 H34 I2 N6 O21 Tb2 Zn | C 1 2/c 1 | 17.2316; 16.7585; 21.2567 90; 106.996; 90 | 5870.3 | Peng-Fei Shi; Huan-Cheng Hu; Zhan-Yun Zhang; Gang Xiong; Bin Zhao Heterometal-organic frameworks as highly sensitive and highly selective luminescent probes to detect I^-^ ions in aqueous solutions Chem.Commun., 2015, 51, 3985 |
7116604 | CIF | C21 H21 As O3 S2 | P 1 21/n 1 | 11.687; 14.366; 12.127 90; 106.254; 90 | 1954.7 | Nikhil Lalwani; Yu-Su Chen; Gemma Brooke; Neil A. Cross; David W. Allen; Alan Reynolds; Jesus Ojeda; Graham J. Tizzard; Simon J. Coles; Neil Bricklebank Triphenylarsonium-functionalised gold nanoparticles: potential nanocarriers for intracellular therapeutics Chem.Commun., 2015, 51, 4109 |
7116605 | CIF | C23 H24 As Br O S | P 1 21/n 1 | 11.17; 13.6075; 14.4757 90; 91.738; 90 | 2199.23 | Nikhil Lalwani; Yu-Su Chen; Gemma Brooke; Neil A. Cross; David W. Allen; Alan Reynolds; Jesus Ojeda; Graham J. Tizzard; Simon J. Coles; Neil Bricklebank Triphenylarsonium-functionalised gold nanoparticles: potential nanocarriers for intracellular therapeutics Chem.Commun., 2015, 51, 4109 |
7116606 | CIF | C116 Cl4 Fe N7 O72 Si2 W18 | C 1 2/c 1 | 35.5945; 14.4862; 38.2599 90; 113.9; 90 | 18036.3 | Rinta Sato; Kosuke Suzuki; Takuo Minato; Masahiro Shinoe; Kazuya Yamaguchi; Noritaka Mizuno Field-induced slow magnetic relaxation of octahedrally coordinated mononuclear Fe(III)-, Co(II)-, and Mn(III)-containing polyoxometalates Chem.Commun., 2015, 51, 4081 |
7116607 | CIF | C124 Cl12 Co N7 O70 Si2 W18 | P -1 | 14.6616; 18.7039; 19.0694 106.86; 92.59; 98.25 | 4931.97 | Rinta Sato; Kosuke Suzuki; Takuo Minato; Masahiro Shinoe; Kazuya Yamaguchi; Noritaka Mizuno Field-induced slow magnetic relaxation of octahedrally coordinated mononuclear Fe(III)-, Co(II)-, and Mn(III)-containing polyoxometalates Chem.Commun., 2015, 51, 4081 |
7116608 | CIF | C114 Mn N7 O74 Si2 W18 | C 1 2/c 1 | 35.6567; 14.4553; 38.3421 90; 113.89; 90 | 18069.4 | Rinta Sato; Kosuke Suzuki; Takuo Minato; Masahiro Shinoe; Kazuya Yamaguchi; Noritaka Mizuno Field-induced slow magnetic relaxation of octahedrally coordinated mononuclear Fe(III)-, Co(II)-, and Mn(III)-containing polyoxometalates Chem.Commun., 2015, 51, 4081 |
7116609 | CIF | C42 H36 N6 O7 Zn4 | P -3 c 1 | 14.5525; 14.5525; 24.7573 90; 90; 120 | 4540.56 | D. Prochowicz; K. Sokolowski; I. Justyniak; A. Kornowicz; D. Fairen-Jimenez; T. Friscic; J. Lewinski A mechanochemical strategy for IRMOF assembly based on pre-designed oxo-zinc precursors Chem.Commun., 2015, 51, 4032 |
7116610 | CIF | C14 H22 F N2 O5 P | P 1 21 1 | 7.71; 12.999; 17.692 90; 92.506; 90 | 1771.4 | Inmaculada Serrano; David Monge; Eleuterio Alvarez; Rosario Fernandez; Jose M. Lassaletta Asymmetric organocatalytic synthesis of quaternary alpha-hydroxy phosphonates: en route to alpha-aryl phosphaisoserines Chem.Commun., 2015, 51, 4077 |
7116614 | CIF | C34 H25 B Te | P -1 | 11.3756; 12.5651; 19.3584 82.926; 75.15; 77.945 | 2608.5 | Fu An Tsao; Alan. J. Lough; Douglas W. Stephan Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether Chem.Commun., 2015, 51, 4287 |
7116615 | CIF | C34 H10 B F15 Te | P -1 | 12.4545; 13.2182; 20.2994 74.416; 73.514; 81.701 | 3078.2 | Fu An Tsao; Alan. J. Lough; Douglas W. Stephan Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether Chem.Commun., 2015, 51, 4287 |
7116616 | CIF | C34 H15 B F10 Te | P -1 | 11.3615; 11.5042; 13.1803 77.723; 66.878; 69.212 | 1475.82 | Fu An Tsao; Alan. J. Lough; Douglas W. Stephan Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether Chem.Commun., 2015, 51, 4287 |
7116617 | CIF | C68 H30 B2 F20 Te2 | C 1 2/c 1 | 39.238; 21.195; 20.08 90; 108.82; 90 | 15807 | Fu An Tsao; Alan. J. Lough; Douglas W. Stephan Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether Chem.Commun., 2015, 51, 4287 |
7116618 | CIF | C17 H20 Cl Li N2 O3 | P 21 21 21 | 7.7015; 12.0371; 18.2095 90; 90; 90 | 1688.09 | Krzysztof Ziach; Janusz Jurczak Mirror symmetry breaking upon spontaneous crystallization from a dynamic combinatorial library of macrocyclic imines Chem.Commun., 2015, 51, 4306 |
7116619 | CIF | C37 H40 Cl2 Li2 N4 O14 | P 1 n 1 | 7.6122; 18.1368; 14.751 90; 96.894; 90 | 2021.81 | Krzysztof Ziach; Janusz Jurczak Mirror symmetry breaking upon spontaneous crystallization from a dynamic combinatorial library of macrocyclic imines Chem.Commun., 2015, 51, 4306 |
7116620 | CIF | C39 H52 Cl3 O3 | P -1 | 9.807; 13.8699; 16.6745 109.657; 95.088; 107.141 | 1996.1 | Shafali Arora; Shivali Sharma; Venus S. Mithu; Chang Hee-Lee; Kamaljit Singh Selective functionalization of methylene bridges of calix[6]arenes. Isolation and identification of stable conformers of methyl ether of p-tert-butylcalix[6]arene Chem.Commun., 2015, 51, 4227 |
7116621 | CIF | C78 H92 O6 | P -1 | 13.323; 16.3491; 17.448 72.532; 84.273; 89.557 | 3606.2 | Shafali Arora; Shivali Sharma; Venus S. Mithu; Chang Hee-Lee; Kamaljit Singh Selective functionalization of methylene bridges of calix[6]arenes. Isolation and identification of stable conformers of methyl ether of p-tert-butylcalix[6]arene Chem.Commun., 2015, 51, 4227 |
7116622 | CIF | C55 H55 Cl3 N8 | P -1 | 10.6574; 14.7322; 17.013 66.539; 80.163; 80.329 | 2399.5 | Koushik Acharyya; Partha Sarathi Mukherjee Shape and size directed self-selection in organic cage formation Chem.Commun., 2015, 51, 4241 |
7116623 | CIF | C48 H42 N4 O6 | P -3 c 1 | 13.5006; 13.5006; 29.691 90; 90; 120 | 4686.6 | Koushik Acharyya; Partha Sarathi Mukherjee Shape and size directed self-selection in organic cage formation Chem.Commun., 2015, 51, 4241 |
7116624 | CIF | C56 H56 Cl6 N8 O3 | P 1 21/c 1 | 17.6515; 27.369; 11.1516 90; 102.653; 90 | 5256.5 | Koushik Acharyya; Partha Sarathi Mukherjee Shape and size directed self-selection in organic cage formation Chem.Commun., 2015, 51, 4241 |
7116625 | CIF | C33 H36 N4 O6 | P 1 21/n 1 | 7.2035; 18.776; 21.734 90; 91.764; 90 | 2938.2 | Koushik Acharyya; Partha Sarathi Mukherjee Shape and size directed self-selection in organic cage formation Chem.Commun., 2015, 51, 4241 |
7116626 | CIF | C30 H46 Ge2 N4 Se3 | P 1 21/c 1 | 16.736; 11.336; 18.978 90; 106.354; 90 | 3454.8 | Surendar Karwasara; Dhirendra Yadav; Chandan Kumar Jha; Gopalan Rajaraman; Selvarajan Nagendran Single-step conversion of silathiogermylene to germaacid anhydrides: unusual reactivity Chem.Commun., 2015, 51, 4310 |
7116627 | CIF | C30 H46 Ge2 N4 S3 | P 1 21/c 1 | 16.4; 11.364; 18.733 90; 106.005; 90 | 3355.9 | Surendar Karwasara; Dhirendra Yadav; Chandan Kumar Jha; Gopalan Rajaraman; Selvarajan Nagendran Single-step conversion of silathiogermylene to germaacid anhydrides: unusual reactivity Chem.Commun., 2015, 51, 4310 |
7116628 | CIF | C26 H27 Cl2 Cu N5 O3 | P -1 | 10.671; 11.025; 11.868 89.45; 77.812; 79.52 | 1341.4 | Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch Chem.Commun., 2015, 51, 4267 |
7116629 | CIF | C20 H13 Cl Cu F3 N3 O4 S | P 1 21/c 1 | 7.59; 20.098; 13.487 90; 94.218; 90 | 2051.8 | Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch Chem.Commun., 2015, 51, 4267 |
7116630 | CIF | C28 H29 Cl2 Cu N5 O2 | P -1 | 10.758; 10.951; 12.045 87.424; 78.339; 79.489 | 1366.4 | Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch Chem.Commun., 2015, 51, 4267 |
7116631 | CIF | C26 H27 Cl2 Cu N5 O2 S | P -1 | 10.634; 10.982; 11.926 89.311; 77.918; 79.929 | 1340.5 | Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch Chem.Commun., 2015, 51, 4267 |
7116632 | CIF | C16 H8 N4 | P 1 21/c 1 | 4.6304; 14.479; 8.886 90; 90.402; 90 | 595.7 | Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines Chem.Commun., 2015, 51, 4275 |
7116633 | CIF | C16 H7 Cl N4 | P 1 21/n 1 | 3.8176; 18.9603; 8.7979 90; 95.327; 90 | 634.07 | Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines Chem.Commun., 2015, 51, 4275 |
7116634 | CIF | C16 H6 Cl2 N4 | P 1 21/n 1 | 3.8194; 19.4986; 8.9236 90; 99.974; 90 | 654.52 | Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines Chem.Commun., 2015, 51, 4275 |
7116635 | CIF | C16 H4 Cl2 N4 | P -1 | 4.7573; 7.941; 8.892 92.898; 100.56; 94.347 | 328.6 | Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines Chem.Commun., 2015, 51, 4275 |
7116636 | CIF | C16 H4 Cl4 N4 | P -1 | 5.8383; 6.0989; 10.5832 82.636; 76.077; 82.498 | 360.8 | Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines Chem.Commun., 2015, 51, 4275 |
7116637 | CIF | C46 H50 Cl6 Ir2 N4 | P -1 | 7.991; 9.776; 15.449 100.26; 102.15; 103.55 | 1113.7 | Nem Singh; Jae-Ho Jo; Young Ho Song; Hyunuk Kim; Dongwook Kim; Myoung Soo Lah; Ki-Whan Chi Coordination-driven self-assembly of an iridium-cornered prismatic cage and encapsulation of three heteroguests in its large cavity Chem.Commun., 2015, 51, 4492 |
7116638 | CIF | C254 H220 F18 Ir6 N24 O21 S6 | P 1 21/n 1 | 27.189; 30.491; 29.069 90; 100.26; 90 | 23713 | Nem Singh; Jae-Ho Jo; Young Ho Song; Hyunuk Kim; Dongwook Kim; Myoung Soo Lah; Ki-Whan Chi Coordination-driven self-assembly of an iridium-cornered prismatic cage and encapsulation of three heteroguests in its large cavity Chem.Commun., 2015, 51, 4492 |
7116639 | CIF | C256 H208 Ir6 N26 O4 | I -4 2 d | 46.154; 46.154; 49.592 90; 90; 90 | 105640 | Nem Singh; Jae-Ho Jo; Young Ho Song; Hyunuk Kim; Dongwook Kim; Myoung Soo Lah; Ki-Whan Chi Coordination-driven self-assembly of an iridium-cornered prismatic cage and encapsulation of three heteroguests in its large cavity Chem.Commun., 2015, 51, 4492 |
7116640 | CIF | C17 H14 O4 | P 1 21/n 1 | 7.761; 9.02; 21.077 90; 97.965; 90 | 1461.2 | Juan Du; Xiuli Zhang; Xi Sun; Lei Wang Copper-catalyzed direct alpha-ketoesterification of propiophenones with acetophenones via C(sp^3^)-H oxidative cross-coupling Chem.Commun., 2015, 51, 4372 |
7116641 | CIF | C32 H22 N2 | P 1 21/n 1 | 14.6334; 8.9414; 17.7375 90; 105.381; 90 | 2237.7 | Wei Huang; Lu Sun; Zhiwen Zheng; Jianhua Su; He Tian Colour-tunable fluorescence of single molecules based on the vibration induced emission of phenazine Chem.Commun., 2015, 51, 4462 |
7116642 | CIF | C16 H23 B F4 Fe N6 | P 1 21/n 1 | 13.0808; 10.6982; 14.0524 90; 96.336; 90 | 1954.5 | Dong Shao; Shao-Liang Zhang; Xin-Hua Zhao; Xin-Yi Wang Spin canting, metamagnetism, and single-chain magnetic behaviour in a cyano-bridged homospin iron(II) compound Chem.Commun., 2015, 51, 4360 |
7116643 | CIF | C42 H36 B3 N3 O6 | P 1 | 7.3418; 15.788; 31.0079 83.135; 87.475; 89.797 | 3564.96 | Xiao-Ye Wang; Fang-Dong Zhuang; Xin-Chang Wang; Xiao-Yu Cao; Jie-Yu Wang; Jian Pei Synthesis, structure and properties of C3-symmetric heterosuperbenzene with three BN units Chem.Commun., 2015, 51, 4368 |
7116644 | CIF | C232.5 H188 F52.5 N20.5 O P16.75 Pd4 Ru2 | P -1 | 23.8865; 25.4288; 31.7818 96.15; 107.106; 113.591 | 16341.8 | Jiajia Yang; Mohan Bhadbhade; William A. Donald; Hasti Iranmanesh; Evan G. Moore; Hong Yan; Jonathon E. Beves Self-assembled supramolecular cages containing ruthenium(II) polypyridyl complexes Chem.Commun., 2015, 51, 4465 |
7116645 | CIF | C63 H45 F7.5 N11 O2 P1.25 Ru | C 1 2/c 1 | 31.584; 16.937; 26.449 90; 105.27; 90 | 13649 | Jiajia Yang; Mohan Bhadbhade; William A. Donald; Hasti Iranmanesh; Evan G. Moore; Hong Yan; Jonathon E. Beves Self-assembled supramolecular cages containing ruthenium(II) polypyridyl complexes Chem.Commun., 2015, 51, 4465 |
7116646 | CIF | C15 H18 I N O2 | P 1 21/n 1 | 9.3649; 15.0028; 11.1821 90; 92.996; 90 | 1568.93 | H.Q. Nimal Gunaratne; Peter Nockemann; Kenneth R. Seddon Pro-fragrant ionic liquids with stable hemiacetal motifs: water-triggered release of fragrances Chem.Commun., 2015, 51, 4455 |
7116647 | CIF | C24 H23 Cl O8 | P -1 | 9.2814; 11.711; 12.1339 113.081; 96.35; 102.204 | 1158.1 | Hong Lu; Jin-Yu Liu; Chen-Guang Li; Jun-Bing Lin; Yong-Min Liang; Peng-Fei Xu A new chiral C1-symmetric NHC-catalyzed addition to alpha-aryl substituted alpha,beta-disubstituted enals: enantioselective synthesis of fully functionalized dihydropyranones Chem.Commun., 2015, 51, 4473 |
7116648 | CIF | C14 H14 Br2 N2 | C 2 2 21 | 7.3088; 31.966; 12.46 90; 90; 90 | 2911.1 | Yusuke Kita; Kosuke Higashida; Kenta Yamaji; Atsuhiro Iimuro; Kazushi Mashima Asymmetric hydrogenation of quinazolinium salts catalysed by halide-bridged dinuclear iridium complexes bearing chiral diphosphine ligands Chem.Commun., 2015, 51, 4380 |
7116649 | CIF | C72 H76 Br2 Ir2 N4 | P 1 21 1 | 14.4388; 14.3302; 14.9599 90; 94.1029; 90 | 3087.43 | Yusuke Kita; Kosuke Higashida; Kenta Yamaji; Atsuhiro Iimuro; Kazushi Mashima Asymmetric hydrogenation of quinazolinium salts catalysed by halide-bridged dinuclear iridium complexes bearing chiral diphosphine ligands Chem.Commun., 2015, 51, 4380 |
7116650 | CIF | C30 H23 Br N2 O3 S | P 1 21/c 1 | 15.2526; 8.7689; 19.1451 90; 90.857; 90 | 2560.3 | Yuanhao Wang; Xiaoqiang Lei; Yefeng Tang Rh(II)-catalyzed cycloadditions of 1-tosyl 1,2,3-triazoles with 2H-azirines: switchable reactivity of Rh-azavinylcarbene as [2C]- or aza-[3C]-synthon Chem.Commun., 2015, 51, 4507 |
7116651 | CIF | C29 H24 N2 O2 S | P 1 21/c 1 | 13.7344; 11.3573; 15.3726 90; 95.591; 90 | 2386.5 | Yuanhao Wang; Xiaoqiang Lei; Yefeng Tang Rh(II)-catalyzed cycloadditions of 1-tosyl 1,2,3-triazoles with 2H-azirines: switchable reactivity of Rh-azavinylcarbene as [2C]- or aza-[3C]-synthon Chem.Commun., 2015, 51, 4507 |
7116652 | CIF | C20 H23 N O6 S2 | P 1 21 1 | 9.1418; 9.388; 12.6939 90; 110.69; 90 | 1019.17 | Chao Song; Wen Yang; Nannan Zhou; Rui Qian; Yajun Zhang; Kaiyan Lou; Rui Wang; Wei Wang Fluorescent theranostic agents for Hg2+ detection and detoxification treatment Chem.Commun., 2015, 51, 4443 |
7116653 | CIF | C98 H126 O6 | P -1 | 10.3348; 19.1818; 22.503 80.708; 78.639; 78.993 | 4257.4 | Liang Han; Yuewei Zhang; Weiping Chen; Xiao Cheng; Kaiqing Ye; Jingying Zhang; Yue Wang Assembly of twisted luminescent architectures based on acenaphtho[1,2-k]fluoranthene derivatives Chem.Commun., 2015, 51, 4477 |
7116654 | CIF | C74 H66 B F27 Ir N6 O6 | P -1 | 14.2926; 17.57617; 30.9787 96.4495; 91.4551; 106.009 | 7420.04 | Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes Chem.Commun., 2015, 51, 4425 |
7116655 | CIF | C71 H58 B Cl2 F26 Ir N6 O4 | P 1 21/n 1 | 19.5682; 18.7483; 20.39 90; 104.772; 90 | 7233.2 | Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes Chem.Commun., 2015, 51, 4425 |
7116656 | CIF | C77 H70 B F26 Ir N6 O6 | P 1 21/c 1 | 20.7249; 22.1162; 18.7709 90; 116.331; 90 | 7711.1 | Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes Chem.Commun., 2015, 51, 4425 |
7116657 | CIF | C71 H63 B F27 Ir N6 O6 | P -1 | 14.3353; 17.5209; 30.9758 95.9306; 91.1596; 106.158 | 7423 | Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes Chem.Commun., 2015, 51, 4425 |
7116658 | CIF | C67 H63 B F24 Ir N7 O6 | P 1 21/c 1 | 13.782; 20.0926; 25.2535 90; 91.1355; 90 | 6991.73 | Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes Chem.Commun., 2015, 51, 4425 |
7116659 | CIF | C15 H22 B F N2 | P -1 | 7.486; 9.564; 10.597 75.8; 76.99; 75.35 | 700.8 | Masahito Murai; Tetsuya Omura; Yoichiro Kuninobu; Kazuhiko Takai Rhenium-catalysed dehydrogenative borylation of primary and secondary C(sp^3^)-H bonds adjacent to a nitrogen atom Chem.Commun., 2015, 51, 4583 |
7116660 | CIF | C46 H79 Fe9 N2 O50 | P 32 2 1 | 18.927; 18.927; 24.693 90; 90; 120 | 7661 | Jiong-Peng Zhao; Song-De Han; Xue Jiang; Jian Xu; Ze Chang; Xian-He Bu A three dimensional magnetically frustrated metal-organic framework via the vertices augmentation of underlying net Chem.Commun., 2015, 51, 4627 |
7116661 | CIF | C H N O | P 21 21 21 | 10.5611; 15.5632; 22.4083 90; 90; 90 | 3683.1 | Pei-Qiang Huang; Su-Yu Huang; Long-Hui Gao; Zhong-Yi Mao; Zong Chang; Ai-E Wang Enantioselective total synthesis of (+)-methoxystemofoline and (+)-isomethoxystemofoline Chem.Commun., 2015, 51, 4576 |
7116662 | CIF | C70 H110 Li2 O2 Pb2 Si4 | P -1 | 12.2658; 16.7325; 20.375 99.254; 107.15; 107.882 | 3654.6 | Masaichi Saito; Marisa Nakada; Takuya Kuwabara; Mao Minoura A reversible two-electron redox system involving a divalent lead species Chem.Commun., 2015, 51, 4674 |
7116663 | CIF | C36 H56 Li2 O2 Pb Si2 | P -1 | 12.4117; 12.4449; 13.7628 82.874; 67.352; 75.447 | 1898.1 | Masaichi Saito; Marisa Nakada; Takuya Kuwabara; Mao Minoura A reversible two-electron redox system involving a divalent lead species Chem.Commun., 2015, 51, 4674 |
7116664 | CIF | C16 H17 N O2 S | P 1 21/n 1 | 14.3451; 5.6024; 19.171 90; 110.01; 90 | 1447.7 | Xiang-Wei Liu; Jiang-Ling Shi; Jiang-Bo Wei; Chao Yang; Jia-Xuan Yan; Kun Peng; Le Dai; Chen-Guang Li; Bi-Qin Wang; Zhang-Jie Shi Diversified syntheses of multifunctionalized thiazole derivatives via regioselective and programmed C-H activation Chem.Commun., 2015, 51, 4599 |
7116665 | CIF | Fe1.172 H Li0.828 O S | P 4/n m m :1 | 3.7038; 3.7038; 8.8852 90; 90; 90 | 121.888 | U. Pachmayr; D. Johrendt [(Li0.8Fe0.2)OH]FeS and the ferromagnetic superconductors [(Li0.8Fe0.2)OH]Fe(S1-xSex) (0 < x ? 1) Chem.Commun., 2015, 51, 4689 |
7116666 | CIF | C148 H96 Mn6 N20 O18 | P 1 21/c 1 | 27.159; 13.925; 41.043 90; 112.375; 90 | 14353 | L. A. Barrios; J. Salinas-Uber; O. Roubeau; S. J. Teat; G. Aromi Molecular self-recognition: a chiral [Mn(II)6] wheel via donor-acceptor pi^...^pi contacts and H-bonds Chem.Commun., 2015, 51, 4631 |
7116667 | CIF | C49 H62 N6 O3 | P 1 21/n 1 | 14.623; 16.641; 18.326 90; 101.777; 90 | 4365.6 | L. A. Barrios; J. Salinas-Uber; O. Roubeau; S. J. Teat; G. Aromi Molecular self-recognition: a chiral [Mn(II)6] wheel via donor-acceptor pi^...^pi contacts and H-bonds Chem.Commun., 2015, 51, 4631 |
7116668 | CIF | C72 H96 O Si4 | P 21 21 21 | 13.7114; 19.2562; 25.0769 90; 90; 90 | 6621 | Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene Chem.Commun., 2015, 51, 4607 |
7116669 | CIF | C72 H98 O2 Si4 | P 1 21/c 1 | 13.426; 18.425; 28.086 90; 94.327; 90 | 6928 | Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene Chem.Commun., 2015, 51, 4607 |
7116670 | CIF | C67.2 H91.2 N1.6 O2.4 Si3.2 | P 1 21/c 1 | 13.31; 29.8304; 19.4965 90; 93.59; 90 | 7725.8 | Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene Chem.Commun., 2015, 51, 4607 |
7116671 | CIF | C72 H96 O Si4 | P 1 21/c 1 | 19.768; 21.986; 16.67 90; 111.807; 90 | 6727 | Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene Chem.Commun., 2015, 51, 4607 |
7116672 | CIF | C72 H98 O2 Si4 | P -1 | 13.171; 14.918; 17.544 85.743; 79.779; 84.496 | 3371 | Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene Chem.Commun., 2015, 51, 4607 |
7116688 | CIF | C29 H28 Cl2 N P Ru S | P 1 21/n 1 | 12.6476; 11.7959; 18.6459 90; 102.933; 90 | 2711.21 | Zhang, Hui-Jun; Lin, Weidong; Wu, Zhengjian; Ruan, Wenqing; Wen, Ting-Bin Silver-mediated direct phosphorylation of benzothiazoles and thiazoles with diarylphosphine oxides. Chemical communications (Cambridge, England), 2015, 51, 3450-3453 |
7116689 | CIF | C15 H12 N O P S | C 1 2/c 1 | 10.4363; 13.1058; 20.7087 90; 96.816; 90 | 2812.44 | Zhang, Hui-Jun; Lin, Weidong; Wu, Zhengjian; Ruan, Wenqing; Wen, Ting-Bin Silver-mediated direct phosphorylation of benzothiazoles and thiazoles with diarylphosphine oxides. Chemical communications (Cambridge, England), 2015, 51, 3450-3453 |
7116702 | CIF | C27 H22 N4 O8 Zn | P 1 21/c 1 | 11.361; 15.532; 16.269 90; 94.661; 90 | 2861.3 | Bappaditya Gole; Udishnu Sanyal; Partha Sarathi Mukherjee A smart approach to achieve an exceptionally high loading of metal nanoparticles supported by functionalized extended frameworks for efficient catalysis Chem.Commun., 2015, 51, 4872 |
7116703 | CIF | C23 H14 N2 O5 Zn | C 1 2/c 1 | 29.971; 16.271; 15.804 90; 115.749; 90 | 6942 | Bappaditya Gole; Udishnu Sanyal; Partha Sarathi Mukherjee A smart approach to achieve an exceptionally high loading of metal nanoparticles supported by functionalized extended frameworks for efficient catalysis Chem.Commun., 2015, 51, 4872 |
7116706 | CIF | C25 H24 N2 O | P -1 | 9.491; 9.5574; 10.9648 91.766; 93.926; 97.631 | 982.69 | Subban Kathiravan; Shishir Ghosh; Graeme Hogarth; Ian A. Nicholls Copper catalysed amidation of aryl halides through chelation assistance Chem.Commun., 2015, 51, 4834 |
7116707 | CIF | C19 H20 N2 O S | P 1 21/c 1 | 16.8737; 9.68667; 10.28958 90; 96.9165; 90 | 1669.59 | Subban Kathiravan; Shishir Ghosh; Graeme Hogarth; Ian A. Nicholls Copper catalysed amidation of aryl halides through chelation assistance Chem.Commun., 2015, 51, 4834 |
7116708 | CIF | C23 H40 Cl Ir N2 | P 1 21/n 1 | 11.8497; 12.2144; 16.718 90; 91.591; 90 | 2418.8 | Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin A simple access to transition metal cyclopropenylidene complexes Chem.Commun., 2015, 51, 4778 |
7116709 | CIF | C15 H28 Cl Cu N2 | P 1 21/c 1 | 6.043; 18.944; 15.635 90; 100.45; 90 | 1760.2 | Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin A simple access to transition metal cyclopropenylidene complexes Chem.Commun., 2015, 51, 4778 |
7116710 | CIF | C30.5 H57 Cl5 N4 Pd2 | P -1 | 8.6743; 15.139; 15.947 86.794; 85.946; 80.765 | 2059.7 | Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin A simple access to transition metal cyclopropenylidene complexes Chem.Commun., 2015, 51, 4778 |
7116711 | CIF | C15 H28 Au Cl N2 | P 1 21/n 1 | 11.3202; 12.8913; 12.5373 90; 90.2151; 90 | 1829.6 | Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin A simple access to transition metal cyclopropenylidene complexes Chem.Commun., 2015, 51, 4778 |
7116712 | CIF | C31 H56 Au F3 N4 O3 S | P 1 21/c 1 | 13.2941; 9.5096; 14.5324 90; 93.61; 90 | 1833.56 | Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin A simple access to transition metal cyclopropenylidene complexes Chem.Commun., 2015, 51, 4778 |
7116713 | CIF | C6 H6 Fe Na3 O17 | C 1 2/c 1 | 17.4212; 12.5545; 14.9217 90; 101.047; 90 | 3203.1 | Qingchun Ge; Tai-Shung Chung Oxalic acid complexes: promising draw solutes for forward osmosis (FO) in protein enrichment Chem.Commun., 2015, 51, 4854 |
7116714 | CIF | C6 H10 Cr Na3 O17 | C 1 2/c 1 | 17.2551; 12.4639; 15.1228 90; 100.454; 90 | 3198.4 | Qingchun Ge; Tai-Shung Chung Oxalic acid complexes: promising draw solutes for forward osmosis (FO) in protein enrichment Chem.Commun., 2015, 51, 4854 |
7116715 | CIF | C24 H18 | P n a 21 | 7.4869; 19.718; 11.2222 90; 90; 90 | 1656.7 | Lingzhi Li; Ming Chen; Haoke Zhang; Han Nie; Jing Zhi Sun; Anjun Qin; Ben Zhong Tang Influence of the number and substitution position of phenyl groups on the aggregation-enhanced emission of benzene-cored luminogens Chem.Commun., 2015, 51, 4830 |
7116716 | CIF | C20 H25 N | P 21 21 21 | 10.529; 11.655; 12.596 90; 90; 90 | 1545.7 | Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters Chem.Commun., 2015, 51, 4793 |
7116717 | CIF | C26 H29 N S | P 1 21/c 1 | 7.535; 14.973; 18.844 90; 95.77; 90 | 2115.2 | Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters Chem.Commun., 2015, 51, 4793 |
7116718 | CIF | C20 H25 N S | P 1 21/n 1 | 8.104; 8.358; 24.688 90; 96.2; 90 | 1662.4 | Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters Chem.Commun., 2015, 51, 4793 |
7116719 | CIF | C20 H25 N S | P 1 21/n 1 | 7.812; 11.736; 18.668 90; 96.49; 90 | 1700.5 | Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters Chem.Commun., 2015, 51, 4793 |
7116720 | CIF | C32 H28 O4 | P 1 21/n 1 | 10.2761; 15.204; 15.2549 90; 96.857; 90 | 2366.34 | Murat Cakici; Zhi-Gang Gu; Martin Nieger; Jochen Burck; Lars Heinke; Stefan Brase Planar-chiral building blocks for metal-organic frameworks Chem.Commun., 2015, 51, 4796 |
7116729 | CIF | C48.93 H35.72 Cu2 N2 O8.93 | P -1 | 10.7482; 12.23; 16.366 95.11; 96.968; 102.936 | 2066.2 | Yuichi Takasaki; Satoshi Takamizawa Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption Chem.Commun., 2015, 51, 5024 |
7116730 | CIF | C48 H32 Cu2 N2 O8 | P -1 | 10.4745; 11.6064; 17.037 97.583; 104.918; 90.081 | 1982.5 | Yuichi Takasaki; Satoshi Takamizawa Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption Chem.Commun., 2015, 51, 5024 |
7116731 | CIF | C48 H32 Cu2 N2 O8 | P -1 | 10.6065; 11.6485; 17.4513 80.612; 75.215; 89.821 | 2055.1 | Yuichi Takasaki; Satoshi Takamizawa Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption Chem.Commun., 2015, 51, 5024 |
7116732 | CIF | C36 H24 Co3 N13 Na O15.25 | P 63 | 13.1191; 13.1191; 16.014 90; 90; 120 | 2386.92 | Ru-Xin Yao; Xin Cui; Jun Wang; Xian-Ming Zhang A homochiral magnet based on D3 symmetric [(NaO3)Co3] clusters: from spontaneous resolution to absolute chiral induction Chem.Commun., 2015, 51, 5108 |
7116733 | CIF | C36 H27 Co3 N13 Na O15 | P 63 | 13.1177; 13.1177; 16.005 90; 90; 120 | 2385.07 | Ru-Xin Yao; Xin Cui; Jun Wang; Xian-Ming Zhang A homochiral magnet based on D3 symmetric [(NaO3)Co3] clusters: from spontaneous resolution to absolute chiral induction Chem.Commun., 2015, 51, 5108 |
7116734 | CIF | C6 H5 B K N3 | P -1 | 9.5267; 9.9704; 10.1727 81.041; 68.165; 83.636 | 884.51 | Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile Chem.Commun., 2015, 51, 4989 |
7116735 | CIF | C28 H36 B4 K4 N12 O2 | P 1 21/c 1 | 7.5693; 25.062; 22.116 90; 94.3; 90 | 4183.6 | Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile Chem.Commun., 2015, 51, 4989 |
7116736 | CIF | C9 B F5 K N3 | P 1 21/c 1 | 11.894; 12.782; 7.5458 90; 103.98; 90 | 1113.2 | Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile Chem.Commun., 2015, 51, 4989 |
7116737 | CIF | C6 H5 B K N3 | P -1 | 9.5044; 9.976; 10.1345 81.033; 68.217; 83.514 | 879.8 | Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile Chem.Commun., 2015, 51, 4989 |
7116738 | CIF | C9 H8 B2 K2 N6 O | P 1 21/n 1 | 9.8586; 13.1307; 12.1811 90; 93.991; 90 | 1573.02 | Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile Chem.Commun., 2015, 51, 4989 |
7116739 | CIF | C26.5 H36.5 Br2 Fe N3.5 O1.5 | P 1 21 1 | 15.777; 10.03; 17.685 90; 100.09; 90 | 2755.3 | Ziqing Zuo; Lei Zhang; Xuebing Leng; Zheng Huang Iron-catalyzed asymmetric hydrosilylation of ketones Chem.Commun., 2015, 51, 5073 |
7116740 | CIF | C47 H45 Br2 Fe N3 O | P 4 | 33.2315; 33.2315; 18.2906 90; 90; 90 | 20198.9 | Ziqing Zuo; Lei Zhang; Xuebing Leng; Zheng Huang Iron-catalyzed asymmetric hydrosilylation of ketones Chem.Commun., 2015, 51, 5073 |
7116741 | CIF | C2 H10 B10 N2 Na2 O17 | C 1 2/c 1 | 21.9507; 6.4172; 11.0598 90; 103.407; 90 | 1515.45 | Jun-Hua Wang; Qi Wei; Jian-Wen Cheng; Huan He; Bai-Feng Yang; Guo-Yu Yang Na2B10O17^.^H2en: a three-dimensional open-framework layered borate co-templated by inorganic cations and organic amines Chem.Commun., 2015, 51, 5066 |
7116742 | CIF | C32 H33 Fe N4 O9.5 | P 1 21 1 | 8.4996; 14.4218; 26.0595 90; 97.616; 90 | 3166.2 | R. Gautam; E. A. Akam; A. V. Astashkin; J. J. Loughrey; E. Tomat Sirtuin inhibitor sirtinol is an intracellular iron chelator Chem.Commun., 2015, 51, 5104 |
7116743 | CIF | C69 H118 N12 Na7 | I -4 2 d | 32.759; 32.759; 29.376 90; 90; 90 | 31525 | Andreas Stascha A pyrazolate-stabilized sodium hydride complex Chem.Commun., 2015, 51, 5056 |
7116744 | CIF | C12.17 H20.33 N2 Na | P 1 21/c 1 | 15.184; 19.831; 26.107 90; 100.11; 90 | 7739 | Andreas Stascha A pyrazolate-stabilized sodium hydride complex Chem.Commun., 2015, 51, 5056 |
7116745 | CIF | C56 H38 Cu2 N3 O11 | P -1 | 16.1748; 17.1245; 17.3765 61.699; 79.187; 79.168 | 4135.1 | Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman Multi-responsive metal-organic lantern cages in solution Chem.Commun., 2015, 51, 5077 |
7116746 | CIF | C150.55 H187.34 Cu4 N5.82 O34.04 | P 1 21/c 1 | 18.2648; 27.0741; 16.6959 90; 110.078; 90 | 7754.4 | Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman Multi-responsive metal-organic lantern cages in solution Chem.Commun., 2015, 51, 5077 |
7116747 | CIF | C136.45 H149.05 Cu4 N16.15 O34.15 | C 1 2/c 1 | 22.7256; 27.998; 23.4326 90; 91.88; 90 | 14901.5 | Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman Multi-responsive metal-organic lantern cages in solution Chem.Commun., 2015, 51, 5077 |
7116748 | CIF | C108 H84 Cu4 N4 O24.61 S4 | P -1 | 14.935; 16.106; 16.995 105.989; 109.453; 104.285 | 3437 | Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman Multi-responsive metal-organic lantern cages in solution Chem.Commun., 2015, 51, 5077 |
7116749 | CIF | C21 H44 Li N5 | P b c a | 10.5102; 18.8729; 23.8796 90; 90; 90 | 4736.7 | Stuart D. Robertson; Alan R. Kennedy; John J. Liggat; Robert E. Mulvey Facile synthesis of a genuinely alkane-soluble but isolable lithium hydride transfer reagent Chem.Commun., 2015, 51, 5452 |
7116750 | CIF | C30 H31 B O2 Zr | P b c a | 10.3097; 15.5055; 32.3133 90; 90; 90 | 5165.51 | Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions Chem.Commun., 2015, 51, 5444 |
7116751 | CIF | C20 H21 B O2 Te | P b c a | 8.2167; 20.788; 22.069 90; 90; 90 | 3769.6 | Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions Chem.Commun., 2015, 51, 5444 |
7116752 | CIF | C20 H14 Te | P -1 | 5.7439; 11.1587; 12.0325 80.1921; 87.5978; 79.981 | 748.3 | Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions Chem.Commun., 2015, 51, 5444 |
7116753 | CIF | C28 H34 B2 O4 Te | P 1 21/n 1 | 10.6313; 21.4729; 13.1595 90; 113.042; 90 | 2764.4 | Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions Chem.Commun., 2015, 51, 5444 |
7116754 | CIF | C28 H34 B2 O4 Te | P -1 | 7.0792; 12.1454; 16.953 75.2698; 82.0304; 80.2126 | 1382.2 | Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions Chem.Commun., 2015, 51, 5444 |
7116755 | CIF | C18 H18 B Cu F5 N4 O3 | I 1 2/a 1 | 15.4006; 9.5362; 28.09 90; 90.988; 90 | 4124.8 | Cameron M. Moore; Nathaniel K. Szymczak Redox-induced fluoride ligand dissociation stabilized by intramolecular hydrogen bonding Chem.Commun., 2015, 51, 5490 |
7116756 | CIF | C18 H18 Cu F N4 O3 | P 1 21/n 1 | 8.793; 14.8014; 13.3814 90; 93.525; 90 | 1738.28 | Cameron M. Moore; Nathaniel K. Szymczak Redox-induced fluoride ligand dissociation stabilized by intramolecular hydrogen bonding Chem.Commun., 2015, 51, 5490 |
7116757 | CIF | C15 H11 N O3 | P b c a | 9.89; 7.3; 32.941 90; 90; 90 | 2378.2 | Soumitra Agasti; Upendra Sharma; Togati Naveen; Debabrata Maiti Orthogonal selectivity with cinnamic acids in 3-substituted benzofuran synthesis through C-H olefination of phenols Chem.Commun., 2015, 51, 5375 |
7116758 | CIF | C34 H36 B2 F15 Li O6 | P 1 21/n 1 | 12.4374; 19.273; 15.5445 90; 93.373; 90 | 3719.7 | Junhao Zheng; Yuwen Wang; Zhen Hua Li; Huadong Wang Application of a nucleophilic boryl complex in the frustrated Lewis pair: activation of H-H, B-H and C[double bond, length as m-dash]C bonds with B(C6F5)3 and boryl-borate lithium Chem.Commun., 2015, 51, 5505 |
7116759 | CIF | C23 H23 N3 O7 | P 1 21 1 | 8.223; 20.352; 14.3 90; 105.02; 90 | 2311.4 | Audrey Dumoulin; Claudia Lalli; Pascal Retailleau; Geraldine Masson Catalytic, highly enantioselective, direct amination of enecarbamates Chem.Commun., 2015, 51, 5383 |
7116760 | CIF | C25 H48 B11 Li N2 O3 | P n m a | 15.1947; 12.6157; 16.666 90; 90; 90 | 3194.74 | Matthew J. Asay; Steven P. Fisher; Sarah E. Lee; Fook S. Tham; Dan Borchardt; Vincent Lavallo Synthesis of unsymmetrical N-carboranyl NHCs: directing effect of the carborane anion Chem.Commun., 2015, 51, 5359 |
7116761 | CIF | C34.93 H66.85 B11 Li2 N2 O5.48 | P n n 2 | 15.9089; 26.7369; 10.561 90; 90; 90 | 4492.2 | Matthew J. Asay; Steven P. Fisher; Sarah E. Lee; Fook S. Tham; Dan Borchardt; Vincent Lavallo Synthesis of unsymmetrical N-carboranyl NHCs: directing effect of the carborane anion Chem.Commun., 2015, 51, 5359 |
7116762 | CIF | C13 H19 N O3 S | P 21 21 21 | 11.3743; 14.0235; 18.6496 90; 90; 90 | 2974.75 | Pablo Barrio; Elsa Rodriguez; Kodai Saito; Santos Fustero; Takahiko Akiyama Gamma-Silylboronates in the chiral Bronsted acid-catalysed allylboration of aldehydes Chem.Commun., 2015, 51, 5246 |
7116763 | CIF | C37 H51 F3 Mn N7 O4 S | P -1 | 13.1912; 13.5415; 23.494 93.278; 103.037; 104.963 | 3920.1 | Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo Chem.Commun., 2015, 51, 5310 |
7116764 | CIF | C48 H74 K Mn N7 O4 | P 1 21/c 1 | 23.141; 9.7932; 22.661 90; 105.914; 90 | 4938.7 | Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo Chem.Commun., 2015, 51, 5310 |
7116765 | CIF | C40 H59 Mn N7 O2 | P 1 21/c 1 | 9.7762; 9.2337; 42.2828 90; 90.193; 90 | 3816.9 | Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo Chem.Commun., 2015, 51, 5310 |
7116766 | CIF | C42 H59 F6 Mn N7 O7 S2 | P 21 21 21 | 10.6932; 16.2784; 27.67 90; 90; 90 | 4816.5 | Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo Chem.Commun., 2015, 51, 5310 |
7116767 | CIF | C8 H26 Fe3 N6 Se4 | C 2 2 21 | 9.1399; 18.122; 11.5436 90; 90; 90 | 1912 | Joshua T. Greenfield; Chongin Pak; Saeed Kamali; Kathleen Lee; Kirill Kovnir Control over connectivity and magnetism of tetrahedral FeSe2 chains through coordination Fe-amine complexes Chem.Commun., 2015, 51, 5355 |
7116768 | CIF | C6 H18 Fe3 N4 Se4 | P 1 21/c 1 | 9.0393; 10.6303; 16.641 90; 102.652; 90 | 1560.2 | Joshua T. Greenfield; Chongin Pak; Saeed Kamali; Kathleen Lee; Kirill Kovnir Control over connectivity and magnetism of tetrahedral FeSe2 chains through coordination Fe-amine complexes Chem.Commun., 2015, 51, 5355 |
7116769 | CIF | C21 H21 I N O3 | P -1 | 11.5839; 15.7615; 32.762 91.604; 91.02; 101.055 | 5866.7 | K. Ackermann; A. Giannoulis; D. B. Cordes; A. M. Z. Slawin; B. E. Bode Assessing dimerisation degree and cooperativity in a biomimetic small-molecule model by pulsed EPR Chem.Commun., 2015, 51, 5257 |
7116770 | CIF | C44.5 H36 Cl N4 O3 | P 42/n :2 | 36.726; 36.726; 5.6924 90; 90; 90 | 7678 | K. Ackermann; A. Giannoulis; D. B. Cordes; A. M. Z. Slawin; B. E. Bode Assessing dimerisation degree and cooperativity in a biomimetic small-molecule model by pulsed EPR Chem.Commun., 2015, 51, 5257 |
7116771 | CIF | C14 H30 N2 O23 U2 | P -1 | 6.2109; 9.997; 11.3778 97.9088; 93.7875; 104.294 | 674.38 | M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions Chem.Commun., 2015, 51, 5306 |
7116772 | CIF | C16 H34 N2 O24 U2 | P -1 | 6.3074; 10.0063; 11.992 94.6846; 98.8324; 104.503 | 718.32 | M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions Chem.Commun., 2015, 51, 5306 |
7116773 | CIF | C22 H30 N2 O22 U2 | P -1 | 6.7978; 9.8815; 11.7825 100.662; 99.5051; 91.0417 | 766.15 | M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions Chem.Commun., 2015, 51, 5306 |
7116774 | CIF | C60 H96 N12 Na4 O94 U6 | P -1 | 19.987; 20.5879; 21.1208 68.467; 64.419; 67.96 | 7044.4 | M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions Chem.Commun., 2015, 51, 5306 |
7116775 | CIF | C36 H27 Mg3 Na5 O81 U9 | P 63/m | 17.4123; 17.4123; 17.8443 90; 90; 120 | 4685.4 | M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions Chem.Commun., 2015, 51, 5306 |
7116776 | CIF | C66 H55 N2 Np O7 P5 | P 1 21/n 1 | 13.61157; 16.5891; 26.4952 90; 91.6657; 90 | 5980.19 | Sean D. Woodall; Adam N. Swinburne; Nidhu lal Banik; Andrew Kerridge; Poppy Di Pietro; Christian Adam; Peter Kaden; Louise S. Natrajan Neptunyl(VI) centred visible LMCT emission directly observable in the presence of uranyl(VI) Chem.Commun., 2015, 51, 5402 |
7116777 | CIF | C67 H57 Cl2 N2 O7 P5 U | P 1 21/n 1 | 9.7808; 23.697; 26.1815 90; 95.334; 90 | 6042 | Sean D. Woodall; Adam N. Swinburne; Nidhu lal Banik; Andrew Kerridge; Poppy Di Pietro; Christian Adam; Peter Kaden; Louise S. Natrajan Neptunyl(VI) centred visible LMCT emission directly observable in the presence of uranyl(VI) Chem.Commun., 2015, 51, 5402 |
7116778 | CIF | C23 H47 B Fe O2 P2 | P n m a | 13.8799; 16.5053; 11.7284 90; 90; 90 | 2686.9 | Thomas J. Mazzacano; Neal P. Mankad Thermal C-H borylation using a CO-free iron boryl complex Chem.Commun., 2015, 51, 5379 |
7116779 | CIF | C17 H35 B Fe O8 P2 | P 1 21/c 1 | 10.5518; 14.372; 16.31 90; 108.637; 90 | 2343.7 | Thomas J. Mazzacano; Neal P. Mankad Thermal C-H borylation using a CO-free iron boryl complex Chem.Commun., 2015, 51, 5379 |
7116780 | CIF | C23 H24 B F18 Fe O8 P3 | P 1 21/n 1 | 10.7235; 18.0733; 18.7761 90; 100.2; 90 | 3581.5 | Thomas J. Mazzacano; Neal P. Mankad Thermal C-H borylation using a CO-free iron boryl complex Chem.Commun., 2015, 51, 5379 |
7116781 | CIF | C24 H36 N5 O Re S4 | P -1 | 11.5743; 11.7501; 12.5007 86.489; 86.743; 60.987 | 1483.23 | Yan, Yong; Mague, Joel T.; Donahue, James P.; Sproules, Stephen Unprecedented Spin Localisation in a Paramagnetic Dirhenium Complex with Multiple Metal Bonds Chem.Commun., 2015, 51, 5482 |
7116782 | CIF | C17 H20 O4 | P 1 21/n 1 | 8.3539; 11.145; 16.1987 90; 101.731; 90 | 1476.67 | M. Presset; B. Michelet; R. Guillot; C. Bour; S. Bezzenine-Lafollee; V. Gandon Gallium(III)- and calcium(II)-catalyzed Meyer-Schuster rearrangements followed by intramolecular aldol condensation or endo-Michael addition Chem.Commun., 2015, 51, 5318 |
7116783 | CIF | C26 H29 F12 N7 O2 P2 Pd | P 1 21/c 1 | 17.4973; 9.579; 20.1652 90; 98.859; 90 | 3339.5 | Michael R. Chapman; Christopher M. Pask; Alireza Ariafard; Charlotte E. Willans sigma-Alkenyl endo-palladacycle formation via regiospecific functionalisation of an unreactive NHC-tethered C(sp2)-H bond Chem.Commun., 2015, 51, 5513 |
7116784 | CIF | C14 H15 F6 N4 O P Pd | P 1 21/m 1 | 12.097; 6.8619; 21.461 90; 91.882; 90 | 1780.5 | Michael R. Chapman; Christopher M. Pask; Alireza Ariafard; Charlotte E. Willans sigma-Alkenyl endo-palladacycle formation via regiospecific functionalisation of an unreactive NHC-tethered C(sp2)-H bond Chem.Commun., 2015, 51, 5513 |
7116785 | CIF | C14 H15 F6 N4 O Pd Sb | P 1 21 1 | 13.0668; 6.8152; 21.0073 90; 90.568; 90 | 1870.7 | Michael R. Chapman; Christopher M. Pask; Alireza Ariafard; Charlotte E. Willans sigma-Alkenyl endo-palladacycle formation via regiospecific functionalisation of an unreactive NHC-tethered C(sp2)-H bond Chem.Commun., 2015, 51, 5513 |
7116786 | CIF | C13 H13 N O | P 21 21 21 | 5.018; 11.717; 18.072 90; 90; 90 | 1062.6 | Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation Chem.Commun., 2015, 51, 5314 |
7116787 | CIF | C13 H13 N O | P 1 21/c 1 | 9.4905; 4.937; 21.8359 90; 95.103; 90 | 1019.06 | Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation Chem.Commun., 2015, 51, 5314 |
7116788 | CIF | C13 H13 N O | P 1 21/n 1 | 10.5236; 7.17; 13.5856 90; 93.912; 90 | 1022.7 | Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation Chem.Commun., 2015, 51, 5314 |
7116789 | CIF | C13 H13 N O | P 1 21/c 1 | 4.918; 17.5881; 11.975 90; 97.432; 90 | 1027.12 | Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation Chem.Commun., 2015, 51, 5314 |
7116790 | CIF | C13 H13 N O | P 1 21/n 1 | 9.3763; 6.5586; 16.7932 90; 102.558; 90 | 1008 | Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation Chem.Commun., 2015, 51, 5314 |
7116791 | CIF | C13 H13 N O | P 1 21/n 1 | 12.7256; 5.4479; 14.793 90; 103.039; 90 | 999.12 | Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation Chem.Commun., 2015, 51, 5314 |
7116792 | CIF | C13 H13 N O | P b c a | 14.6822; 6.6231; 20.97 90; 90; 90 | 2039.2 | Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation Chem.Commun., 2015, 51, 5314 |
7116793 | CIF | C50 H61 Cu N4 O2 | P 1 21/c 1 | 19.5203; 11.1949; 20.5166 90; 99.303; 90 | 4424.5 | Vincent Cesar; Valentina Mallardo; Adela Nano; Georges Dahm; Noel Lugan; Guy Lavigne; Stephane Bellemin-Laponnaz IMes-acac: hybrid combination of diaminocarbene and acetylacetonato sub-units into a new anionic ambidentate NHC ligand Chem.Commun., 2015, 51, 5271 |
7116794 | CIF | C50 H62 B Cu F4 N4 O2 | P -1 | 10.373; 18.414; 26.739 96.931; 91.874; 102.56 | 4940 | Vincent Cesar; Valentina Mallardo; Adela Nano; Georges Dahm; Noel Lugan; Guy Lavigne; Stephane Bellemin-Laponnaz IMes-acac: hybrid combination of diaminocarbene and acetylacetonato sub-units into a new anionic ambidentate NHC ligand Chem.Commun., 2015, 51, 5271 |
7116795 | CIF | C13 H31 Cl Cu N4 O6 | P n a 21 | 17.0837; 12.5402; 9.2795 90; 90; 90 | 1988 | Athina Anastasaki; Vasiliki Nikolaou; Francesca Brandford-Adams; Gabit Nurumbetov; Qiang Zhang; Guy J. Clarkson; David J. Fox; Paul Wilson; Kristian Kempe; David M. Haddleton Photo-induced living radical polymerization of acrylates utilizing a discrete copper(II)-formate complex Chem.Commun., 2015, 51, 5626 |
7116796 | CIF | C18 H14 Cu2 N0 O10 | I m m a | 18.8261; 22.1934; 10.0062 90; 90; 90 | 4180.7 | Hui-Min Wen; Bin Li; Hailong Wang; Chuande Wu; Khalid Alfooty; Rajamani Krishna; Banglin Chen A microporous metal-organic framework with rare lvt topology for highly selective C2H2/C2H4 separation at room temperature Chem.Commun., 2015, 51, 5610 |
7116797 | CIF | C35 H41 Cu5 N40 O0 | F d d d | 16.18; 43.077; 45.485 90; 90; 90 | 31702 | B. X. Dong; S. Y. Zhang; W. L. Liu; Y. C. Wu; J. Ge; L. Song; Y. L. Teng Gas storage and separation in a water-stable [Cu^I^5BTT3]^4-^ anion framework comprising a giant multi-prismatic nanoscale cage Chem.Commun., 2015, 51, 5691 |
7116798 | CIF | C36 H51 N O2 Zr | P 1 21 1 | 10.82; 11.235; 15.074 90; 110.637; 90 | 1714.9 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116799 | CIF | C42 H57 N O2 Zr | P 32 | 25.473; 25.473; 15.017 90; 90; 120 | 8439 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116800 | CIF | C50 H57 N O2 Si Zr | P 21 21 21 | 10.4723; 20.7272; 21.2971 90; 90; 90 | 4622.8 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116801 | CIF | C51 H57 N O2 Zr | P 21 21 21 | 9.9279; 20.7319; 20.8378 90; 90; 90 | 4288.9 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116802 | CIF | C53 H61 N O2 Zr | P 1 21 1 | 10.0708; 16.4364; 29.62 90; 91.34; 90 | 4901.6 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116803 | CIF | C56 H59 N O2 Zr | P 1 21 1 | 12.3987; 10.2035; 35.906 90; 91.315; 90 | 4541.3 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116804 | CIF | C50 H55 N O2 Zr | P 1 21 1 | 9.9153; 39.191; 10.9485 90; 93.596; 90 | 4246.1 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116805 | CIF | C49 H51 N O2 Zr | P 1 21 1 | 10.249; 10.086; 20.139 90; 102.78; 90 | 2030.2 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116806 | CIF | C51 H55 N O2 Zr | P 21 21 21 | 10.4071; 20.0669; 20.1804 90; 90; 90 | 4214.4 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116807 | CIF | C53 H59 N O2 Zr | P 21 21 21 | 10.5049; 20.1449; 20.7934 90; 90; 90 | 4400.3 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116808 | CIF | C61 H59 N O2 Zr | P 21 21 21 | 9.9859; 10.2631; 46.379 90; 90; 90 | 4753.2 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116809 | CIF | C44 H43 N O2 Zr | C 1 2/c 1 | 29.258; 24.694; 23.148 90; 117.297; 90 | 14862 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116810 | CIF | C72 H87 N5 O4 Zr2 | P -1 | 12.0652; 13.096; 23.377 100.831; 93.008; 111.473 | 3346.2 | Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism Chem.Commun., 2015, 51, 5751 |
7116811 | CIF | C42 H34 O12 Zn3 | P 32 2 1 | 18.1019; 18.1019; 24.668 90; 90; 120 | 7000.2 | Hongmin Su; Fuxing Sun; Jiangtao Jia; Hongming He; Aifei Wang; Guangshan Zhu A highly porous medical metal-organic framework constructed from bioactive curcumin Chem.Commun., 2015, 51, 5774 |
7116812 | CIF | C13 H14 N2 O7 | P 21 21 21 | 5.0946; 14.4569; 18.2887 90; 90; 90 | 1347 | E.-K. Kim; R. Krishnamurthy Synthesis of orotidine by intramolecular nucleosidation Chem.Commun., 2015, 51, 5618 |
7116813 | CIF | C16 H29 N O7 | P 21 21 21 | 6.1806; 14.641; 20.36 90; 90; 90 | 1842.4 | Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid Chem.Commun., 2015, 51, 5664 |
7116814 | CIF | C17 H31 N O7 | P 21 21 21 | 6.3376; 15.4586; 20.0153 90; 90; 90 | 1960.9 | Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid Chem.Commun., 2015, 51, 5664 |
7116815 | CIF | C24 H31 N O7 | P 21 21 21 | 7.6206; 11.4755; 26.5274 90; 90; 90 | 2319.8 | Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid Chem.Commun., 2015, 51, 5664 |
Back to the search form
Your own data is not in the COD? Deposit it, thanks!