Crystallography Open Database
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Searching journal of publication like 'Chemical communications (Cambridge, England)' volume of publication is 52
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7119037 | CIF | C240 H240 F39 Mn8 N84 P6.5 | P n -3 n :2 | 26.6801; 26.6801; 26.6801 90; 90; 90 | 18991.6 | Jing Yang; Xiao-Yong Chang; Kiu-Chor Sham; Shek-Man Yiu; Hoi-Lun Kwong; Chi-Ming Che M8L12 cubic cages with all facial delta or facial lamda configuration: effects of surface anions on the occupancy of the cage and anion exchange Chem.Commun., 2016, 52, 5981 |
| 7119038 | CIF | C20 H35 N3 O6 | P 21 21 21 | 9.1953; 15.9688; 16.377 90; 90; 90 | 2404.8 | Mihye Lee; Jihyun Shim; Philjae Kang; Moon-Gun Choi; Soo Hyuk Choi Stabilization of 11/9-helical alpha/beta-peptide foldamers in protic solvents Chem.Commun., 2016, 52, 5950 |
| 7119039 | CIF | C29 H49 N5 O8 | P 21 21 21 | 9.7107; 17.8054; 18.6925 90; 90; 90 | 3232 | Mihye Lee; Jihyun Shim; Philjae Kang; Moon-Gun Choi; Soo Hyuk Choi Stabilization of 11/9-helical alpha/beta-peptide foldamers in protic solvents Chem.Commun., 2016, 52, 5950 |
| 7119040 | CIF | C31 H52 Cl3 N5 O8 | P 21 21 21 | 9.5052; 17.583; 23.471 90; 90; 90 | 3922.7 | Mihye Lee; Jihyun Shim; Philjae Kang; Moon-Gun Choi; Soo Hyuk Choi Stabilization of 11/9-helical alpha/beta-peptide foldamers in protic solvents Chem.Commun., 2016, 52, 5950 |
| 7119041 | CIF | C26 H25 N O S | P -1 | 8.28; 11.804; 12.324 64.811; 88.065; 80.753 | 1075 | Jia-Jia Zhao; Man Tang; Hong-Hao Zhang; Meng-Meng Xu; Feng Shi Bronsted acid-catalyzed chemodivergent reactions of ortho-mercaptobenzyl alcohols with 3-alkyl-2-vinylindoles and styrenes: [5+2] cyclization versus hydroxysulfenylation Chem.Commun., 2016, 52, 5953 |
| 7119042 | CIF | C35 H42 O4 S3 | C 1 c 1 | 8.5603; 22.813; 17.3998 90; 94.2688; 90 | 3388.5 | Jia-Jia Zhao; Man Tang; Hong-Hao Zhang; Meng-Meng Xu; Feng Shi Bronsted acid-catalyzed chemodivergent reactions of ortho-mercaptobenzyl alcohols with 3-alkyl-2-vinylindoles and styrenes: [5+2] cyclization versus hydroxysulfenylation Chem.Commun., 2016, 52, 5953 |
| 7119043 | CIF | C20 H14 F4 N2 O2 | P -1 | 11.228; 12.46; 12.943 77.35; 89.67; 86.39 | 1763.2 | Yingle Liu; Ke Zhang; Yangen Huang; Shen Pan; Xiao-Qiang Liu; Yi Yang; Yan Jiang; Xiu-Hua Xu Synthesis of 3-fluoroalkenyl-3-trifluoromethyl-2-oxindoles by the reaction of indoline-2,3-diones with difluoromethylene phosphabetaine Chem.Commun., 2016, 52, 5969 |
| 7119044 | CIF | C14 H8 Fe N6 O2 Pt | C 1 2/c 1 | 15.667; 15.136; 7.3104 90; 110.57; 90 | 1623 | Tomoyuki Haraguchi; Kazuya Otsubo; Osami Sakata; Shogo Kawaguchi; Akihiko Fujiwara; Hiroshi Kitagawa A three-dimensional accordion-like metal∓organic framework: synthesis and unconventional oriented growth on a surface Chem.Commun., 2016, 52, 6017 |
| 7119045 | CIF | C23 H17 N O4 S | P 1 21 1 | 8.33; 12.431; 9.528 90; 93.09; 90 | 985.2 | Zhuang Song; Yizhou Wu; Tao Xin; Chao Jin; Xiaoan Wen; Hongbin Sun; Qing-Long Xu The Rh(II)-catalyzed formal N-S bond insertion reaction of aryldiazoacetates into N-phenyl-sulfenyl phthalimide Chem.Commun., 2016, 52, 6079 |
| 7119046 | CIF | C467 Ag120 B4 Cl4 F64 N10 O45 S24 Si8 | C 1 2/m 1 | 43.889; 31.033; 26.186 90; 123.512; 90 | 29737 | Zi-Yi Chen; Dennis Y. S. Tam; Thomas C. W. Mak Ethynide-stabilized high-nuclearity silver(I) sulfido molecular clusters assembled using organic sulfide precursors Chem.Commun., 2016, 52, 6119 |
| 7119047 | CIF | C198 Ag46 B2 F8 N2 O14 S6 | P 1 21/n 1 | 19.8433; 28.203; 23.1207 90; 97.808; 90 | 12819.3 | Zi-Yi Chen; Dennis Y. S. Tam; Thomas C. W. Mak Ethynide-stabilized high-nuclearity silver(I) sulfido molecular clusters assembled using organic sulfide precursors Chem.Commun., 2016, 52, 6119 |
| 7119048 | CIF | C62.5 H75 Cl3 F5 N5 O W | P 1 21/c 1 | 11.2444; 26.1267; 20.6154 90; 94.991; 90 | 6033.4 | Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes Chem.Commun., 2016, 52, 6099 |
| 7119049 | CIF | C40.5 H58 Cl F6 N5 O6 S2 W | P -1 | 11.7112; 20.3641; 21.9201 103.305; 97.459; 100.855 | 4913.7 | Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes Chem.Commun., 2016, 52, 6099 |
| 7119050 | CIF | C55 H76 Cl2 N4 W | P -1 | 10.5591; 13.627; 21.2326 86.879; 81.476; 88.576 | 3016.47 | Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes Chem.Commun., 2016, 52, 6099 |
| 7119051 | CIF | C58.5 H79 Cl8 N5 W | P 1 21/c 1 | 21.6865; 18.8737; 16.1005 90; 106.667; 90 | 6313.1 | Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes Chem.Commun., 2016, 52, 6099 |
| 7119052 | CIF | C124 H90 F40 N12 | P -1 | 16.634; 18.391; 18.849 88.309; 76.986; 82.645 | 5571.9 | Won-Young Cha; Takanori Soya; Takayuki Tanaka; Hirotaka Mori; Yongseok Hong; Sangsu Lee; Kyu Hyung Park; Atsuhiro Osuka; Dongho Kim Multifaceted [36]octaphyrin(1.1.1.1.1.1.1.1): deprotonation-induced switching among nonaromatic, Mobius aromatic, and Huckel antiaromatic species Chem.Commun., 2016, 52, 6076 |
| 7119053 | CIF | C182 H256 N2 O16 P8 Ru4 | P 1 21/c 1 | 16.1117; 26.6027; 21.6003 90; 100.029; 90 | 9116.7 | Daniel Fink; Bernhard Weibert; Rainer F. Winter Redox-active tetraruthenium metallacycles: reversible release of up to eight electrons resulting in strong electrochromism Chem.Commun., 2016, 52, 6103 |
| 7119054 | CIF | C148 H234 Cl16 N2 O16 P8 Ru4 | P -1 | 11.6168; 16.816; 23.594 94.41; 99.289; 107.587 | 4297.1 | Daniel Fink; Bernhard Weibert; Rainer F. Winter Redox-active tetraruthenium metallacycles: reversible release of up to eight electrons resulting in strong electrochromism Chem.Commun., 2016, 52, 6103 |
| 7119055 | CIF | C72 H64 Cl4 N2 P2 Ru2 | P 1 | 10.3736; 13.2432; 13.7718 99.178; 107.636; 97.263 | 1748.99 | Demyan E. Prokopchuk; Alan J. Lough; Rafael E. Rodriguez-Lugo; Robert H. Morris; Hansjorg Grutzmacher Insights into metal-ligand hydrogen transfer: a square-planar ruthenate complex supported by a tetradentate amino-amido-diolefin ligand Chem.Commun., 2016, 52, 6138 |
| 7119056 | CIF | C40 H42 N2 O Ru | P 1 21/c 1 | 9.121; 15.475; 21.72 90; 92.615; 90 | 3062.5 | Demyan E. Prokopchuk; Alan J. Lough; Rafael E. Rodriguez-Lugo; Robert H. Morris; Hansjorg Grutzmacher Insights into metal-ligand hydrogen transfer: a square-planar ruthenate complex supported by a tetradentate amino-amido-diolefin ligand Chem.Commun., 2016, 52, 6138 |
| 7119057 | CIF | C56 H73 K N2 O8 Ru | P 1 21/c 1 | 11.8733; 24.8708; 17.2324 90; 95.965; 90 | 5061.1 | Demyan E. Prokopchuk; Alan J. Lough; Rafael E. Rodriguez-Lugo; Robert H. Morris; Hansjorg Grutzmacher Insights into metal-ligand hydrogen transfer: a square-planar ruthenate complex supported by a tetradentate amino-amido-diolefin ligand Chem.Commun., 2016, 52, 6138 |
| 7119058 | CIF | C35 H39 Br N2 O9 | P 21 21 21 | 12.919; 15.875; 17.332 90; 90; 90 | 3554.6 | Bo-Liang Zhao; Da-Ming Du Organocatalytic cascade Michael/Michael reaction for the asymmetric synthesis of spirooxindoles containing five contiguous stereocenters Chem.Commun., 2016, 52, 6162 |
| 7119059 | CIF | C30 H27.5 F6 N2.5 O6 S2 | P 1 21 1 | 11.6454; 12.5993; 21.7275 90; 104.608; 90 | 3084.9 | Jaroslav Sebestik; Filip Teply; Ivana Cisarova; Jan Vavra; Dusan Koval; Petr Bour Intense chirality induction in nitrile solvents by a helquat dye monitored by near resonance Raman scattering Chem.Commun., 2016, 52, 6257 |
| 7119060 | CIF | C28 H29 I2 N3 O2 | P 21 21 21 | 7.9386; 17.6476; 19.6814 90; 90; 90 | 2757.31 | Jaroslav Sebestik; Filip Teply; Ivana Cisarova; Jan Vavra; Dusan Koval; Petr Bour Intense chirality induction in nitrile solvents by a helquat dye monitored by near resonance Raman scattering Chem.Commun., 2016, 52, 6257 |
| 7119061 | CIF | C41 H38 Dy F9 N14 O9 S3 | P b c a | 20.8179; 19.5864; 24.4923 90; 90; 90 | 9986.7 | Zhong-Xia Jiang; Jun-Liang Liu; Yan-Cong Chen; Jiang Liu; Jian-Hua Jia; Ming-Liang Tong Lanthanoid single-ion magnets with the LnN10 coordination geometry Chem.Commun., 2016, 52, 6261 |
| 7119062 | CIF | C41 H38 Er F9 N14 O9 S3 | P b c a | 20.69; 19.5456; 24.427 90; 90; 90 | 9878.2 | Zhong-Xia Jiang; Jun-Liang Liu; Yan-Cong Chen; Jiang Liu; Jian-Hua Jia; Ming-Liang Tong Lanthanoid single-ion magnets with the LnN10 coordination geometry Chem.Commun., 2016, 52, 6261 |
| 7119064 | CIF | C40 H40 Cl4 Cu4 N2 P2 | P 1 21/c 1 | 11.1272; 13.525; 13.4866 90; 104.147; 90 | 1968.11 | Xu-Lin Chen; Rongmin Yu; Xiao-Yuan Wu; Dong Liang; Ji-Hui Jia; Can-Zhong Lu A strongly greenish-blue-emitting Cu4Cl4 cluster with an efficient spin-orbit coupling (SOC): fast phosphorescence versus thermally activated delayed fluorescence Chem.Commun., 2016, 52, 6288 |
| 7119065 | CIF | C22 H18 N2 O3 S | P 1 21/n 1 | 9.4353; 17.316; 11.6428 90; 92.321; 90 | 1900.7 | Ming Chen; Ning Sun; Haoyi Chen; Yuanhong Liu Dioxazoles, a new mild nitrene transfer reagent in gold catalysis: highly efficient synthesis of functionalized oxazoles Chem.Commun., 2016, 52, 6324 |
| 7119066 | CIF | C23 H18 N2 O3 S2 | P 1 21/c 1 | 18.929; 12.43; 8.472 90; 91.235; 90 | 1992.9 | Ming Chen; Ning Sun; Haoyi Chen; Yuanhong Liu Dioxazoles, a new mild nitrene transfer reagent in gold catalysis: highly efficient synthesis of functionalized oxazoles Chem.Commun., 2016, 52, 6324 |
| 7119067 | CIF | C29 H36 Au F6 N3 O4 S2 | P 32 2 1 | 11.4418; 11.4418; 23.88 90; 90; 120 | 2707.4 | Ming Chen; Ning Sun; Haoyi Chen; Yuanhong Liu Dioxazoles, a new mild nitrene transfer reagent in gold catalysis: highly efficient synthesis of functionalized oxazoles Chem.Commun., 2016, 52, 6324 |
| 7119068 | CIF | C94.45 H106.45 N6 P2 | P -1 | 12.2213; 16.2437; 22.0973 97.7; 93.029; 106.714 | 4144.2 | Alexander Hinz; Axel Schulz; Alexander Villinger On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases Chem.Commun., 2016, 52, 6328 |
| 7119069 | CIF | C56.95 H58.95 Au Cl N2 P2 | P -1 | 10.94; 11.9932; 21.421 87.907; 76.158; 65.57 | 2478.4 | Alexander Hinz; Axel Schulz; Alexander Villinger On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases Chem.Commun., 2016, 52, 6328 |
| 7119070 | CIF | C51 H53 Au1.33 Cl1.33 N2 P2 | P -1 | 11.168; 12.029; 18.686 94.538; 94.411; 114.833 | 2254.1 | Alexander Hinz; Axel Schulz; Alexander Villinger On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases Chem.Commun., 2016, 52, 6328 |
| 7119071 | CIF | C51 H53 Au1.44 Cl1.44 N2 P2 | P -1 | 11.243; 12.0524; 18.7795 94.113; 94.288; 114.879 | 2287.1 | Alexander Hinz; Axel Schulz; Alexander Villinger On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases Chem.Commun., 2016, 52, 6328 |
| 7119072 | CIF | C25 H14 F N O4 | P 1 21/c 1 | 9.7639; 19.413; 10.4751 90; 105.633; 90 | 1912.1 | Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold Chem.Commun., 2016, 52, 6280 |
| 7119073 | CIF | C26 H17 N O5 | P 21 21 21 | 11.2312; 16.239; 22.524 90; 90; 90 | 4108 | Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold Chem.Commun., 2016, 52, 6280 |
| 7119074 | CIF | C25 H13 F2 N O4 | P 1 21/c 1 | 10.033; 19.091; 10.544 90; 107.453; 90 | 1926.6 | Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold Chem.Commun., 2016, 52, 6280 |
| 7119075 | CIF | C25 H13 Cl F N O4 | P -1 | 9.9815; 10.7217; 10.8522 66.536; 86.529; 76.874 | 1036.9 | Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold Chem.Commun., 2016, 52, 6280 |
| 7119076 | CIF | C20 H12 F N O5 | P -1 | 11.727; 12.81; 12.935 103.837; 115.433; 91.903 | 1683.3 | Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold Chem.Commun., 2016, 52, 6280 |
| 7119077 | CIF | C21 H14 Cl N O5 | C 1 2/c 1 | 22.142; 15.2704; 12.2599 90; 115.973; 90 | 3726.6 | Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold Chem.Commun., 2016, 52, 6280 |
| 7119078 | CIF | C30 H21 N3 O5 | P 1 21/c 1 | 12.8577; 14.7678; 16.2529 90; 112.154; 90 | 2858.3 | Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold Chem.Commun., 2016, 52, 6280 |
| 7119079 | CIF | C25 H17 Cl N2 O5 | P 1 21/n 1 | 11.783; 13.245; 15.8627 90; 94.265; 90 | 2468.8 | Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold Chem.Commun., 2016, 52, 6280 |
| 7119080 | CIF | C27 H39 Cl Cu N | P 1 21/c 1 | 15.9209; 19.4144; 16.2447 90; 103.631; 90 | 4879.72 | Alexander S. Romanov; Dawei Di; Le Yang; Julio Fernandez-Cestau; Ciaran R. Becker; Charlotte E. James; Bonan Zhu; Mikko Linnolahti; Dan Credgington; Manfred Bochmann Highly photoluminescent copper carbene complexes based on prompt rather than delayed fluorescence Chem.Commun., 2016, 52, 6379 |
| 7119081 | CIF | C27.5 H40 Cl Cu I N | P -1 | 11.1918; 11.9685; 20.7901 101.52; 94.798; 94.419 | 2706.59 | Alexander S. Romanov; Dawei Di; Le Yang; Julio Fernandez-Cestau; Ciaran R. Becker; Charlotte E. James; Bonan Zhu; Mikko Linnolahti; Dan Credgington; Manfred Bochmann Highly photoluminescent copper carbene complexes based on prompt rather than delayed fluorescence Chem.Commun., 2016, 52, 6379 |
| 7119082 | CIF | C27 H39 Br Cu N | P 1 21/c 1 | 16.0878; 19.4137; 16.2912 90; 103.54; 90 | 4946.71 | Alexander S. Romanov; Dawei Di; Le Yang; Julio Fernandez-Cestau; Ciaran R. Becker; Charlotte E. James; Bonan Zhu; Mikko Linnolahti; Dan Credgington; Manfred Bochmann Highly photoluminescent copper carbene complexes based on prompt rather than delayed fluorescence Chem.Commun., 2016, 52, 6379 |
| 7119083 | CIF | C18 H14 Fe | P 1 21/c 1 | 13.4447; 19.4178; 9.8391 90; 91.496; 90 | 2567.8 | Antonio Urbano; Gloria Hernandez-Torres; Ana M. del Hoyo; Alicia Martinez-Carrion; M. Carmen Carreno Mild access to planar-chiral ortho-condensed aromatic ferrocenes via gold(I)-catalyzed cycloisomerization of ortho-alkynylaryl ferrocenes Chem.Commun., 2016, 52, 6419 |
| 7119084 | CIF | C19 H16 Fe O | P 41 21 2 | 7.8273; 7.8273; 47.227 90; 90; 90 | 2893.4 | Antonio Urbano; Gloria Hernandez-Torres; Ana M. del Hoyo; Alicia Martinez-Carrion; M. Carmen Carreno Mild access to planar-chiral ortho-condensed aromatic ferrocenes via gold(I)-catalyzed cycloisomerization of ortho-alkynylaryl ferrocenes Chem.Commun., 2016, 52, 6419 |
| 7119085 | CIF | C122 H74 B2 F48 Pd4 | P -1 | 13.2706; 15.2693; 16.3133 101.437; 110.526; 102.271 | 2887.5 | Kohei Masai; Katsunori Shirato; Koji Yamamoto; Yuki Kurashige; Tetsuro Murahashi A mechanistic insight into metal-cluster pi-envelopment: a dual binding mode involving bent and planar ligand-conformers Chem.Commun., 2016, 52, 6427 |
| 7119086 | CIF | C128 H78 B2 Cl2 F48 Pd4 | P -1 | 14.2381; 15.6226; 28.2509 81.3277; 79.8346; 77.6849 | 6001.1 | Kohei Masai; Katsunori Shirato; Koji Yamamoto; Yuki Kurashige; Tetsuro Murahashi A mechanistic insight into metal-cluster pi-envelopment: a dual binding mode involving bent and planar ligand-conformers Chem.Commun., 2016, 52, 6427 |
| 7119087 | CIF | C153 H106 B2 Cl2 F48 Pd4 | P 1 21 1 | 18.5114; 21.0181; 19.5326 90; 111.452; 90 | 7073.2 | Kohei Masai; Katsunori Shirato; Koji Yamamoto; Yuki Kurashige; Tetsuro Murahashi A mechanistic insight into metal-cluster pi-envelopment: a dual binding mode involving bent and planar ligand-conformers Chem.Commun., 2016, 52, 6427 |
| 7119088 | CIF | C27 H21 Au B Cl F4 N P | P 1 21/c 1 | 10.394; 16.6422; 15.389 90; 108.771; 90 | 2520.39 | Long Huang; Frank Rominger; Matthias Rudolph; A. Stephen K. Hashmi A general access to organogold(III) complexes by oxidative addition of diazonium salts Chem.Commun., 2016, 52, 6435 |
| 7119089 | CIF | C27 H20 Au B Cl2 F4 N P | P -1 | 9.3558; 11.4552; 13.9422 86.4666; 70.5144; 67.9291 | 1301.94 | Long Huang; Frank Rominger; Matthias Rudolph; A. Stephen K. Hashmi A general access to organogold(III) complexes by oxidative addition of diazonium salts Chem.Commun., 2016, 52, 6435 |
| 7119090 | CIF | C26.5 H38.5 Au Cl6.5 F3 P | P 1 21/c 1 | 12.1272; 14.5748; 18.6371 90; 96.632; 90 | 3272.09 | Long Huang; Frank Rominger; Matthias Rudolph; A. Stephen K. Hashmi A general access to organogold(III) complexes by oxidative addition of diazonium salts Chem.Commun., 2016, 52, 6435 |
| 7119091 | CIF | C12 H28.5 B10 Br N2.5 | P 1 21/c 1 | 7.6257; 25.7293; 10.2076 90; 92.279; 90 | 2001.19 | Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium Chem.Commun., 2016, 52, 6443 |
| 7119092 | CIF | C11 H27 B9 N2 | P 1 21/c 1 | 15.6541; 13.7503; 18.375 90; 115.101; 90 | 3581.7 | Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium Chem.Commun., 2016, 52, 6443 |
| 7119093 | CIF | C31 H55 B9 N4 Rh2 | P b c a | 11.9249; 23.7834; 25.2349 90; 90; 90 | 7157 | Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium Chem.Commun., 2016, 52, 6443 |
| 7119094 | CIF | C32 H58 B9 N3 O Rh2 | P -1 | 11.1781; 12.5631; 14.8258 111.322; 92.917; 105.326 | 1845.32 | Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium Chem.Commun., 2016, 52, 6443 |
| 7119095 | CIF | C29 H54 B9 N2 O0.5 Rh2 | P -1 | 10.7898; 11.4212; 14.8764 71.73; 83.274; 69.415 | 1629.6 | Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium Chem.Commun., 2016, 52, 6443 |
| 7119096 | CIF | C19 H38 B10 Cl N2 Rh | P 1 21/c 1 | 12.3894; 15.3629; 13.6908 90; 93.441; 90 | 2601.17 | Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium Chem.Commun., 2016, 52, 6443 |
| 7119097 | CIF | C19 H37 B10 N2 Rh | P 1 21/c 1 | 17.2832; 10.5283; 14.1775 90; 113.02; 90 | 2374.34 | Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium Chem.Commun., 2016, 52, 6443 |
| 7119098 | CIF | C27 H38 O3 | P 1 21 1 | 5.8458; 12.3784; 16.7657 90; 98.058; 90 | 1201.22 | Qiqiao Lin; Yuanzhen Li; Deb Kumar Das; Guoxiang Zhang; Zhifei Zhao; Shuang Yang; Xinqiang Fang N-Heterocyclic carbene-catalyzed desymmetrization of functionalized 1,4-dienes via Stetter Reaction Chem.Commun., 2016, 52, 6459 |
| 7119099 | CIF | C384 H288 Cu4.8 N288 Zn43.2 | I a -3 d | 34.4885; 34.4885; 34.4885 90; 90; 90 | 41022.6 | Xiao-Wei Zhu; Xiao-Ping Zhou; Dan Li Exceptionally water stable heterometallic gyroidal MOFs: tuning the porosity and hydrophobicity by doping metal ions Chem.Commun., 2016, 52, 6513 |
| 7119102 | CIF | C47 H82 O5 Si4 | P -1 | 11.8267; 13.4665; 18.3608 106.876; 92.299; 109.501 | 2607.2 | Jian Zhang; Hong Kang; Jacob Martin; Shouhai Zhang; Sylvie Thomas; Tim C. Merkel; Jianyong Jin The enhancement of chain rigidity and gas transport performance of polymers of intrinsic microporosity via intramolecular locking of the spiro-carbon Chem.Commun., 2016, 52, 6553 |
| 7119103 | CIF | C16 H28 O3 | P 21 21 21 | 6.67202; 12.80551; 18.3291 90; 90; 90 | 1566.01 | Yajun Ren; Marc Presset; Jeremy Godemert; Nicolas Vanthuyne; Jean-Valere Naubron; Michel Giorgi; Jean Rodriguez; Yoann Coquerel A switchable dual organocatalytic system and the enantioselective total synthesis of the quadrane sesquiterpene suberosanone Chem.Commun., 2016, 52, 6565 |
| 7119114 | CIF | C17 H16 F3 N O4 S | P -1 | 9.3925; 9.5682; 10.9216 73.528; 66.26; 85.458 | 860.9 | Zhi-Wei Yang; Qi Zhang; Yuan-Ye Jiang; Lei Li; Bin Xiao; Yao Fu Palladium-catalyzed directing group-assisted C8-triflation of naphthalenes Chem.Commun., 2016, 52, 6709 |
| 7119115 | CIF | C45 H68 O3 S Sm2 | P 1 21/c 1 | 10.7989; 23.324; 18.592 90; 106.381; 90 | 4492.7 | Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky Samarocene oxide: from an undesired decomposition product to a new reagent Chem.Commun., 2016, 52, 6654 |
| 7119116 | CIF | C45 H68 O2 S2 Sm2 | P 1 21/n 1 | 18.588; 23.602; 21.654 90; 107.26; 90 | 9072 | Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky Samarocene oxide: from an undesired decomposition product to a new reagent Chem.Commun., 2016, 52, 6654 |
| 7119117 | CIF | C44 H68 O4 S Sm2 | P 1 21/c 1 | 17.824; 16.299; 16.056 90; 108.56; 90 | 4421.9 | Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky Samarocene oxide: from an undesired decomposition product to a new reagent Chem.Commun., 2016, 52, 6654 |
| 7119118 | CIF | C50 H70 N2 O4 S Sm2 | P 1 21/n 1 | 16.952; 13.879; 20.819 90; 90.81; 90 | 4897.7 | Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky Samarocene oxide: from an undesired decomposition product to a new reagent Chem.Commun., 2016, 52, 6654 |
| 7119119 | CIF | C68 H86 O4 Sm2 | P -1 | 10.561; 10.7; 15.035 110.25; 97.77; 98.73 | 1542.9 | Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky Samarocene oxide: from an undesired decomposition product to a new reagent Chem.Commun., 2016, 52, 6654 |
| 7119120 | CIF | C44 H66 N2 O8 Re2 Sm2 | P b c a | 16.207; 14; 21.465 90; 90; 90 | 4870.4 | Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky Samarocene oxide: from an undesired decomposition product to a new reagent Chem.Commun., 2016, 52, 6654 |
| 7119121 | CIF | C34 H25 B O | P -1 | 9.7747; 11.2285; 12.079 86.4386; 70.8147; 85.0255 | 1246.59 | Sam Yruegas; Dayna C. Patterson; Caleb D. Martin Oxygen insertion into boroles as a route to 1,2-oxaborines Chem.Commun., 2016, 52, 6658 |
| 7119122 | CIF | C40 H29 B O | P -1 | 10.5923; 11.7946; 12.5909 91.8608; 94.7506; 113.478 | 1434.13 | Sam Yruegas; Dayna C. Patterson; Caleb D. Martin Oxygen insertion into boroles as a route to 1,2-oxaborines Chem.Commun., 2016, 52, 6658 |
| 7119123 | CIF | C12 H11 Cl N2 O5 S | P -1 | 9.5347; 10.4694; 15.6057 92.938; 107.085; 116.622 | 1300.34 | Cory M. Widdifield; Harry Robson; Paul Hodgkinson Furosemide's one little hydrogen atom: NMR crystallography structure verification of powdered molecular organics Chem.Commun., 2016, 52, 6685 |
| 7119124 | CIF | C31 H20 N2 O | P 1 21/n 1 | 15.6295; 11.7772; 23.646 90; 100.375; 90 | 4281.4 | Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes Chem.Commun., 2016, 52, 6797 |
| 7119125 | CIF | C35 H22 N2 O | P 1 21 1 | 10.417; 7.846; 15.614 90; 109.024; 90 | 1206.5 | Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes Chem.Commun., 2016, 52, 6797 |
| 7119126 | CIF | C31 H20 N2 O3 | P 1 21/n 1 | 10.4123; 10.6141; 22.372 90; 101.14; 90 | 2425.9 | Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes Chem.Commun., 2016, 52, 6797 |
| 7119127 | CIF | C31 H19.46 Cl0.08 N2 O | P 1 21/n 1 | 15.6018; 11.8059; 23.666 90; 100.492; 90 | 4286.2 | Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes Chem.Commun., 2016, 52, 6797 |
| 7119128 | CIF | C24 H21 N O4 S | P 1 21/c 1 | 10.284; 26.1213; 15.8601 90; 102.69; 90 | 4156.4 | Hongxu Liu; Yanyan Yang; Jie Wu; Xiao-Na Wang; Junbiao Chang Regioselective synthesis of 3,4-disubstituted isocoumarins through the Pd-catalyzed annulation of 2-iodoaromatic acids with ynamides Chem.Commun., 2016, 52, 6801 |
| 7119129 | CIF | C30 H25 N O4 S | P -1 | 12.2963; 13.8393; 16.8203 71.704; 82.18; 66.12 | 2484.87 | Hongxu Liu; Yanyan Yang; Jie Wu; Xiao-Na Wang; Junbiao Chang Regioselective synthesis of 3,4-disubstituted isocoumarins through the Pd-catalyzed annulation of 2-iodoaromatic acids with ynamides Chem.Commun., 2016, 52, 6801 |
| 7119130 | CIF | C40 H32 Cl4 P2 Pd | P 1 21/c 1 | 9.8924; 19.0871; 19.8273 90; 100.618; 90 | 3679.63 | Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis Chem.Commun., 2016, 52, 6785 |
| 7119131 | CIF | C41 H32 Cl8 P2 Pt | P 1 21 1 | 9.9582; 21.3845; 10.1108 90; 103.135; 90 | 2096.78 | Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis Chem.Commun., 2016, 52, 6785 |
| 7119132 | CIF | C82 H68 Au2 Cl4 O P4 | P -1 | 12.7889; 16.392; 19.0982 93.515; 96.512; 112.335 | 3655.6 | Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis Chem.Commun., 2016, 52, 6785 |
| 7119133 | CIF | C40 H32 Au2 Cl4 P2 | P 1 21/n 1 | 12.6409; 16.973; 18.0808 90; 104.661; 90 | 3753 | Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis Chem.Commun., 2016, 52, 6785 |
| 7119134 | CIF | C39.5 H31 Au2 Cl3 P2 | C 1 2 1 | 34.8; 9.8414; 10.8355 90; 96.507; 90 | 3687 | Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis Chem.Commun., 2016, 52, 6785 |
| 7119135 | CIF | C39.5 H31 Au2 Cl3 P2 | C 1 2 1 | 34.8079; 9.8397; 10.8227 90; 96.441; 90 | 3683.4 | Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis Chem.Commun., 2016, 52, 6785 |
| 7119136 | CIF | C38 H62 Li4 N2 O4 | P -1 | 8.7871; 9.5833; 13.1959 104.353; 93.696; 116.282 | 945.63 | Quentin Dufrois; Laure Vendier; Michel Etienne alpha-CC agostic structures and aggregation diversity in cyclopropyllithium derivatives Chem.Commun., 2016, 52, 6781 |
| 7119137 | CIF | C33 H49 Li2 O3 | P -1 | 8.5802; 9.438; 20.2265 80.998; 82.494; 70.198 | 1516.79 | Quentin Dufrois; Laure Vendier; Michel Etienne alpha-CC agostic structures and aggregation diversity in cyclopropyllithium derivatives Chem.Commun., 2016, 52, 6781 |
| 7119138 | CIF | C39 H32 B2 F12 N2 S2 | P 1 2/c 1 | 17.8505; 8.3333; 13.1813 90; 104.671; 90 | 1896.84 | Kazuki Takase; Kengo Hyodo; Masakazu Morimoto; Yuko Kojima; Hiroyuki Mayama; Satoshi Yokojima; Shinichiro Nakamura; Kingo Uchida Photoinduced reversible formation of a superhydrophilic surface by crystal growth of diarylethene Chem.Commun., 2016, 52, 6885 |
| 7119139 | CIF | C39 H34 B2 F12 N2 O S2 | P 1 21/c 1 | 9.7143; 32.9243; 11.9342 90; 96.4166; 90 | 3793.08 | Kazuki Takase; Kengo Hyodo; Masakazu Morimoto; Yuko Kojima; Hiroyuki Mayama; Satoshi Yokojima; Shinichiro Nakamura; Kingo Uchida Photoinduced reversible formation of a superhydrophilic surface by crystal growth of diarylethene Chem.Commun., 2016, 52, 6885 |
| 7119140 | CIF | C20 H23 N O3 | P 21 21 21 | 8.6053; 11.6403; 17.468 90; 90; 90 | 1749.7 | Yuan-Ming Sun; Peng Gu; Yu-Ning Gao; Qin Xu; Min Shi Gold(I) catalyzed tandem cyclization of propargylic esters to 4-acyloxy-1,2-dihydroquinolines Chem.Commun., 2016, 52, 6942 |
| 7119141 | CIF | C21 H29 F6 Ir N O P | P 21 21 21 | 7.0929; 15.6774; 20.8647 90; 90; 90 | 2320.12 | Ross A. Arthurs; Peter N. Horton; Simon J. Coles; Christopher J. Richards Metallocene to metallocene conversion. Synthesis of an oxazoline-substituted pentamethyliridocenium cation from a ferrocenyloxazoline Chem.Commun., 2016, 52, 7024 |
| 7119142 | CIF | C14 H8 F2 N4 | P 1 21/c 1 | 4.375; 20.1126; 13.1678 90; 98.317; 90 | 1146.48 | Erchang Shang; Junzhi Zhang; Jinyi Bai; Zhan Wang; Xiang Li; Bing Zhu; Xiaoguang Lei Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation Chem.Commun., 2016, 52, 7028 |
| 7119143 | CIF | C14 H9 N3 O | P c a 21 | 21.401; 4.7059; 10.6453 90; 90; 90 | 1072.1 | Erchang Shang; Junzhi Zhang; Jinyi Bai; Zhan Wang; Xiang Li; Bing Zhu; Xiaoguang Lei Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation Chem.Commun., 2016, 52, 7028 |
| 7119144 | CIF | C16 H14 N4 | P 1 21/n 1 | 5.9753; 15.9285; 13.447 90; 90.062; 90 | 1279.9 | Erchang Shang; Junzhi Zhang; Jinyi Bai; Zhan Wang; Xiang Li; Bing Zhu; Xiaoguang Lei Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation Chem.Commun., 2016, 52, 7028 |
| 7119145 | CIF | C38 H42 F10 P2 Pt Zn | P 1 21/n 1 | 10.9506; 19.9969; 17.6775 90; 96.054; 90 | 3849.4 | Allegra L. Liberman-Martin; Daniel S. Levine; Micah S. Ziegler; Robert G. Bergman; T. Don Tilley Lewis acid-base interactions between platinum(II) diaryl complexes and bis(perfluorophenyl)zinc: strongly accelerated reductive elimination induced by a Z-type ligand Chem.Commun., 2016, 52, 7039 |
| 7119146 | CIF | C51 H42 F10 N2 Pt Zn | P 1 21/c 1 | 12.995; 16.7483; 21.185 90; 106.136; 90 | 4429.1 | Allegra L. Liberman-Martin; Daniel S. Levine; Micah S. Ziegler; Robert G. Bergman; T. Don Tilley Lewis acid-base interactions between platinum(II) diaryl complexes and bis(perfluorophenyl)zinc: strongly accelerated reductive elimination induced by a Z-type ligand Chem.Commun., 2016, 52, 7039 |
| 7119147 | CIF | C56 H40 B | P 1 21/c 1 | 14.436; 9.801; 28.668 90; 100.42; 90 | 3989 | Holger Braunschweig; Ivo Krummenacher; Lisa Mailander; Leanne Pentecost; Alfredo Vargas Formation of a stable radical by oxidation of a tetraorganoborate Chem.Commun., 2016, 52, 7005 |
| 7119148 | CIF | C40.17 H62.43 Na2 O28 | P 1 21 1 | 6.6058; 24.886; 14.6272 90; 102.224; 90 | 2350.08 | Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita A saccharide-based crystalline sponge for hydrophilic guests Chem.Commun., 2016, 52, 7013 |
| 7119149 | CIF | C21 H34 Na O13.5 | P 1 21 1 | 6.6503; 24.44; 14.717 90; 101.39; 90 | 2344.9 | Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita A saccharide-based crystalline sponge for hydrophilic guests Chem.Commun., 2016, 52, 7013 |
| 7119150 | CIF | C20.45 H30.90 Na O14.46 | P 1 21 1 | 6.6481; 24.625; 14.756 90; 102.798; 90 | 2355.7 | Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita A saccharide-based crystalline sponge for hydrophilic guests Chem.Commun., 2016, 52, 7013 |
| 7119151 | CIF | C20.29 H30.59 Na O14 | P 1 21 1 | 6.6239; 24.772; 14.6783 90; 102.43; 90 | 2352.1 | Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita A saccharide-based crystalline sponge for hydrophilic guests Chem.Commun., 2016, 52, 7013 |
| 7119152 | CIF | C2 H6 Cd | P 42/m n m | 7.195; 7.195; 4.118 90; 90; 90 | 213.2 | Hanke, Felix; Hindley, Sarah; Jones, Anthony C.; Steiner, Alexander The solid state structures of the high and low temperature phases of dimethylcadmium Chemical Communications, 2016, 52, 10144 |
| 7119153 | CIF | C2 H6 Cd | P 1 21/n 1 | 7.483; 7.711; 7.734 90; 115.85; 90 | 401.6 | Hanke, Felix; Hindley, Sarah; Jones, Anthony C.; Steiner, Alexander The solid state structures of the high and low temperature phases of dimethylcadmium Chemical Communications, 2016, 52, 10144 |
| 7119160 | CIF | C13 H16 N2 O7 | P 1 21/c 1 | 12.554; 8.8499; 12.6253 90; 103.988; 90 | 1361.1 | Lynne H. Thomas; Craig Wales; Chick C. Wilson Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes Chem.Commun., 2016, 52, 7372 |
| 7119161 | CIF | C7 H8 O6 | P 1 21/n 1 | 3.6803; 27.724; 9.3579 90; 94.397; 90 | 952 | Lynne H. Thomas; Craig Wales; Chick C. Wilson Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes Chem.Commun., 2016, 52, 7372 |
| 7119162 | CIF | C15 H13 N3 O4 S | P -1 | 7.8557; 10.1043; 10.4713 80.602; 68.952; 69.742 | 727.01 | Lynne H. Thomas; Craig Wales; Chick C. Wilson Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes Chem.Commun., 2016, 52, 7372 |
| 7119163 | CIF | C15 H13 N3 O4 S | P -1 | 12.6899; 14.6928; 20.5097 84.866; 74.669; 84.683 | 3663.7 | Lynne H. Thomas; Craig Wales; Chick C. Wilson Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes Chem.Commun., 2016, 52, 7372 |
| 7119164 | CIF | C46 H43 N9 O13 S3 | P -1 | 7.0374; 12.917; 25.467 84.077; 89.174; 83.327 | 2287 | Lynne H. Thomas; Craig Wales; Chick C. Wilson Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes Chem.Commun., 2016, 52, 7372 |
| 7119165 | CIF | C16 H15 N O | P b c a | 9.0171; 11.0071; 23.9483 90; 90; 90 | 2376.9 | Vijay K. Srirambhatla; Rui Guo; Sarah L. Price; Alastair J. Florence Isomorphous template induced crystallisation: a robust method for the targeted crystallisation of computationally predicted metastable polymorphs Chem.Commun., 2016, 52, 7384 |
| 7119166 | CIF | C26 H16 S2 | P 1 21/n 1 | 15.113; 7.708; 16.178 90; 94; 90 | 1880 | Haichao Liu; Liang Yao; Bao Li; Xiankai Chen; Yu Gao; Shitong Zhang; Weijun Li; Ping Lu; Bing Yang; Yuguang Ma Excimer-induced high-efficiency fluorescence due to pairwise anthracene stacking in a crystal with long lifetime Chem.Commun., 2016, 52, 7356 |
| 7119167 | CIF | C26 H16 S2 | C 1 2/c 1 | 17.08; 11.919; 19.8 90; 104.04; 90 | 3910.4 | Haichao Liu; Liang Yao; Bao Li; Xiankai Chen; Yu Gao; Shitong Zhang; Weijun Li; Ping Lu; Bing Yang; Yuguang Ma Excimer-induced high-efficiency fluorescence due to pairwise anthracene stacking in a crystal with long lifetime Chem.Commun., 2016, 52, 7356 |
| 7119168 | CIF | C22 H23 N3 O4 | P 1 21/n 1 | 10.9129; 7.8194; 22.428 90; 97.304; 90 | 1898.3 | Haiyan Yu; Wang Ren; Hongguang Lu; Yanan Liang; Qiusheng Wang Synthesis and piezochromic luminescence study of a coumarin hydrozone compound Chem.Commun., 2016, 52, 7387 |
| 7119169 | CIF | C21 H11 F26 N O2 | P -1 | 12.37; 12.834; 18.49 98.783; 91.487; 104.872 | 2797.3 | Yohei Haketa; Ryota Takasago; Hiromitsu Maeda beta-Perfluoroalkyl-substituted pyrrole as an anion-responsive pi-electronic system through a single NH moiety Chem.Commun., 2016, 52, 7364 |
| 7119170 | CIF | C132 H108 Cd4 N20 O12 | C 1 2/c 1 | 31.093; 34.507; 24.271 90; 128.646; 90 | 20339 | Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi Post-synthetic modifications of cadmium-based knots and links Chem.Commun., 2016, 52, 7398 |
| 7119171 | CIF | C70 H56 B Cd2 F4 N10 O8 | I b a m | 12.5188; 15.3848; 42.5644 90; 90; 90 | 8197.9 | Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi Post-synthetic modifications of cadmium-based knots and links Chem.Commun., 2016, 52, 7398 |
| 7119172 | CIF | C105 H69 Cd3 F9 N15 O24 Re3 | R 3 c :H | 18.6042; 18.6042; 51.5285 90; 90; 120 | 15445.4 | Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi Post-synthetic modifications of cadmium-based knots and links Chem.Commun., 2016, 52, 7398 |
| 7119173 | CIF | C64 H60 F3 N12 O52 P W12 Zn2 | P 4/n :2 | 19.5965; 19.5965; 16.078 90; 90; 90 | 6174.32 | Jian-Zhen Liao; Chen Wu; Xiao-Yuan Wu; Shui-Quan Deng; Can-Zhong Lu Exceptional photosensitivity of a polyoxometalate-based charge-transfer hybrid material Chem.Commun., 2016, 52, 7394 |
| 7119174 | CIF | C18 H16 O4 | P 1 21/c 1 | 11.891; 16.2219; 15.2941 90; 93.262; 90 | 2945.4 | Rajkumar Lalji Sahani; Rai-Shung Liu Gold-catalyzed [4+3] and [4+4]-annulation reactions of t-butyl propiolate derivatives with epoxides and oxetanes for the construction of 1,4-dioxepane and 1,5-dioxocane cores Chem.Commun., 2016, 52, 7482 |
| 7119175 | CIF | C19 H18 O4 | P 1 21/n 1 | 5.7294; 16.4971; 16.9275 90; 96.391; 90 | 1590 | Rajkumar Lalji Sahani; Rai-Shung Liu Gold-catalyzed [4+3] and [4+4]-annulation reactions of t-butyl propiolate derivatives with epoxides and oxetanes for the construction of 1,4-dioxepane and 1,5-dioxocane cores Chem.Commun., 2016, 52, 7482 |
| 7119176 | CIF | Mn1.5 N O13 V4 | P 1 2/m 1 | 8.2011; 3.5207; 9.9129 90; 110.987; 90 | 267.234 | Martin K. Dufficy; Lan Luo; Peter S. Fedkiw; Paul A. Maggard Vacancy-induced manganese vanadates and their potential application to Li-ion batteries Chem.Commun., 2016, 52, 7509 |
| 7119177 | CIF | C12 H8 Co3 K O20 | I -4 2 d | 13.0691; 13.0691; 30.157 90; 90; 90 | 5150.9 | Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons A non-topological mechanism for negative linear compressibility Chem.Commun., 2016, 52, 7486 |
| 7119178 | CIF | C12 H8 Co3 K O18 | I -4 2 d | 13.0005; 13.0005; 30.2002 90; 90; 90 | 5104.2 | Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons A non-topological mechanism for negative linear compressibility Chem.Commun., 2016, 52, 7486 |
| 7119179 | CIF | C12 H8 Co3 K O18 | I -4 2 d | 12.8201; 12.8201; 30.2685 90; 90; 90 | 4974.8 | Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons A non-topological mechanism for negative linear compressibility Chem.Commun., 2016, 52, 7486 |
| 7119180 | CIF | C12 H8 Co3 K O18 | I -4 2 d | 12.6111; 12.6111; 30.2999 90; 90; 90 | 4818.9 | Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons A non-topological mechanism for negative linear compressibility Chem.Commun., 2016, 52, 7486 |
| 7119181 | CIF | C21 H20 O4 | P 21 21 21 | 5.9638; 7.4011; 40.7678 90; 90; 90 | 1799.44 | Wei Zhou; Peng Chen; Mengna Tao; Xiao Su; Qingjie Zhao; Junliang Zhang Enantioselective intermolecular cross Rauhut-Currier reactions of activated alkenes with acrolein Chem.Commun., 2016, 52, 7612 |
| 7119182 | CIF | C39 H38 N O P S | P 21 21 21 | 8.966; 10.6824; 34.6972 90; 90; 90 | 3323.2 | Wei Zhou; Peng Chen; Mengna Tao; Xiao Su; Qingjie Zhao; Junliang Zhang Enantioselective intermolecular cross Rauhut-Currier reactions of activated alkenes with acrolein Chem.Commun., 2016, 52, 7612 |
| 7119183 | CIF | C16 H21 B Fe O2 | P 1 21/n 1 | 12.7414; 7.5452; 15.8499 90; 104.524; 90 | 1475.06 | Anis Tlili; Arnaud Voituriez; Angela Marinetti; Pierre Thuery; Thibault Cantat Synergistic effects in ambiphilic phosphino-borane catalysts for the hydroboration of CO2 Chem.Commun., 2016, 52, 7553 |
| 7119350 | CIF | C6 Cl8 N10 O8 | P 1 21/c 1 | 6.1067; 13.7465; 12.4167 90; 96.024; 90 | 1036.57 | Srinivas, Dharavath; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M. From FOX-7 to H-FOX to insensitive energetic materials with hypergolic properties Chemical Communications, 2016, 52, 7668-7671 |
| 7119351 | CIF | C4 H2 Cl2 N10 O8 | P 1 21/c 1 | 10.3037; 9.6323; 14.3934 90; 107.927; 90 | 1359.17 | Srinivas, Dharavath; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M. From FOX-7 to H-FOX to insensitive energetic materials with hypergolic properties Chemical Communications, 2016, 52, 7668-7671 |
| 7119352 | CIF | C47 H43 Ag3 F6 N12 O7 S2 | P -1 | 12.88; 13.13; 15.88 99.38; 90.29; 101.76 | 2592 | Hui; Guo; Xin; He; Chong-Qing; Wan; Liang; Zhao A stepwise bulk-to-cluster-to-particle transformation toward the efficient synthesis of alkynyl-protected silver nanoclusters Chem.Commun., 2016, 52, 7723 |
| 7119353 | CIF | C24 H27 Br O5 | P 1 21 1 | 11.882; 6.1817; 15.84 90; 108.485; 90 | 1103.4 | Liangliang; Song; Lei; Gong; Eric; Meggers Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex Chem.Commun., 2016, 52, 7699 |
| 7119354 | CIF | C43 H44 N3 O5 Rh | P 21 21 21 | 12.6831; 13.3648; 25.5629 90; 90; 90 | 4333.1 | Liangliang; Song; Lei; Gong; Eric; Meggers Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex Chem.Commun., 2016, 52, 7699 |
| 7119355 | CIF | C24 H27 Br O5 | P 21 21 21 | 6.202; 12.159; 30.276 90; 90; 90 | 2283.12 | Liangliang; Song; Lei; Gong; Eric; Meggers Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex Chem.Commun., 2016, 52, 7699 |
| 7119356 | CIF | C12 H8 I2 N O3 | C 1 2/c 1 | 17.6; 4.372; 34.3 90; 97.444; 90 | 2617 | Subhankar; Saha; Gautam; R.; Desiraju Using structural modularity in cocrystals to engineer properties: elasticity Chem.Commun., 2016, 52, 7676 |
| 7119357 | CIF | C24 H16 Cl4 N2 O6 | P -1 | 3.795; 14.7; 21.4 80.7; 89.35; 89.09 | 1178 | Subhankar; Saha; Gautam; R.; Desiraju Using structural modularity in cocrystals to engineer properties: elasticity Chem.Commun., 2016, 52, 7676 |
| 7119358 | CIF | C11 H8 Br2 N O | P -1 | 4.183; 8.769; 15.366 94.1; 95.78; 99.68 | 550.5 | Subhankar; Saha; Gautam; R.; Desiraju Using structural modularity in cocrystals to engineer properties: elasticity Chem.Commun., 2016, 52, 7676 |
| 7119359 | CIF | C9 H6 Cl2 N O3 | P -1 | 3.777; 10.382; 13.45 68.43; 85.15; 80.26 | 483.3 | Subhankar; Saha; Gautam; R.; Desiraju Using structural modularity in cocrystals to engineer properties: elasticity Chem.Commun., 2016, 52, 7676 |
| 7119360 | CIF | C9 H6 I2 N O3 | C 1 2/c 1 | 27.78; 4.706; 17.566 90; 96.051; 90 | 2284 | Subhankar; Saha; Gautam; R.; Desiraju Using structural modularity in cocrystals to engineer properties: elasticity Chem.Commun., 2016, 52, 7676 |
| 7119361 | CIF | C91.75 H99.7 Cl12.48 N14.43 O4.45 Pd6 S0.48 | P 1 21/c 1 | 19.6264; 52.3974; 14.3627 90; 90.6803; 90 | 14769.2 | Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions Chem.Commun., 2016, 52, 7657 |
| 7119362 | CIF | C43 H52 Cl8 N6 O4 Pd3 | P 1 21/c 1 | 19.5796; 52.142; 14.2469 90; 91.162; 90 | 14541.9 | Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions Chem.Commun., 2016, 52, 7657 |
| 7119363 | CIF | C94.65 H105.36 Cl12 N16.29 O3.82 Pd6 S0.41 | P 1 21/c 1 | 19.5493; 51.784; 14.2759 90; 90.7569; 90 | 14450.8 | Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions Chem.Commun., 2016, 52, 7657 |
| 7119373 | CIF | C13 H17 N3 O3 S2 | P b c a | 10.4816; 12.7531; 22.3603 90; 90; 90 | 2989 | Celia; Ruiz-Palomero; Stuart; R.; Kennedy; M.; Laura; Soriano; Christopher; D.; Jones; Miguel; Valcarcel; Jonathan; W.; Steed Pharmaceutical crystallization with nanocellulose organogels Chem.Commun., 2016, 52, 7782 |
| 7119374 | CIF | C32 H62 N4 O5 S3 | P -1 | 5.7565; 10.7037; 31.057 87.126; 85.544; 86.192 | 1901.7 | Celia; Ruiz-Palomero; Stuart; R.; Kennedy; M.; Laura; Soriano; Christopher; D.; Jones; Miguel; Valcarcel; Jonathan; W.; Steed Pharmaceutical crystallization with nanocellulose organogels Chem.Commun., 2016, 52, 7782 |
| 7119375 | CIF | C20 H15 N O3 | P 21 21 21 | 5.5517; 11.006; 24.121 90; 90; 90 | 1473.8 | Chun-Wei; Kuo; Ashok; Konala; Lyu; Lin; Ting-Ta; Chiang; Chia-Yu; Huang; Tang-Hao; Yang; Veerababurao; Kavala; Ching-Fa; Yao Synthesis of benzo[a]carbazole derivatives from 3-ethylindoles by exploiting the dual character of benzoquinone as an oxidizing agent and dienophile Chem.Commun., 2016, 52, 7870 |
| 7119376 | CIF | C25 H19 N O2 | C 1 2/c 1 | 37.27; 7.992; 12.774 90; 91.797; 90 | 3803 | Chun-Wei; Kuo; Ashok; Konala; Lyu; Lin; Ting-Ta; Chiang; Chia-Yu; Huang; Tang-Hao; Yang; Veerababurao; Kavala; Ching-Fa; Yao Synthesis of benzo[a]carbazole derivatives from 3-ethylindoles by exploiting the dual character of benzoquinone as an oxidizing agent and dienophile Chem.Commun., 2016, 52, 7870 |
| 7119377 | CIF | C20 H15 Cl N2 O2 | P 21 21 21 | 7.174; 14.3271; 17.4194 90; 90; 90 | 1790.4 | Zhu, Gongming; Yang, Junxian; Bao, Guangjun; Zhang, Ming; Li, Jing; Li, Yiping; Sun, Wangsheng; Hong, Liang; Wang, Rui Catalyst-controlled switch of regioselectivity in the asymmetric allylic alkylation of oxazolones with MBHCs Chemical Communications, 2016, 52, 7882-7885 |
| 7119378 | CIF | C21 H18 Cl N O4 | P 21 21 21 | 7.1668; 12.4455; 21.2096 90; 90; 90 | 1891.78 | Zhu, Gongming; Yang, Junxian; Bao, Guangjun; Zhang, Ming; Li, Jing; Li, Yiping; Sun, Wangsheng; Hong, Liang; Wang, Rui Catalyst-controlled switch of regioselectivity in the asymmetric allylic alkylation of oxazolones with MBHCs Chemical Communications, 2016, 52, 7882-7885 |
| 7119379 | CIF | C62 H58 Gd2 N8 O20 Zn2 | P 1 21/c 1 | 13.8176; 14.3073; 16.9982 90; 95.502; 90 | 3344.9 | Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E. Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation Chemical Communications, 2016, 52, 7866-7869 |
| 7119380 | CIF | C62 H58 Dy2 N8 O20 Zn2 | P 1 21/c 1 | 13.75033; 14.3147; 16.9418 90; 95.2801; 90 | 3320.54 | Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E. Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation Chemical Communications, 2016, 52, 7866-7869 |
| 7119381 | CIF | C62 H58 N8 O20 Y2 Zn2 | P 1 21/c 1 | 13.7448; 14.3133; 16.9268 90; 95.068; 90 | 3317 | Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E. Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation Chemical Communications, 2016, 52, 7866-7869 |
| 7119382 | CIF | C62 H58 Eu2 N8 O20 Zn2 | P 1 21/c 1 | 13.8125; 14.3087; 16.9783 90; 95.498; 90 | 3340.14 | Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E. Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation Chemical Communications, 2016, 52, 7866-7869 |
| 7119383 | CIF | C23 H18 N2 | P 1 21/c 1 | 10.0681; 9.7551; 17.5082 90; 94.291; 90 | 1714.8 | Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E. Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation Chemical Communications, 2016, 52, 7866-7869 |
| 7119384 | CIF | C29 H24 N2 O2 | P -1 | 9.9468; 10.285; 11.5735 75.327; 82.383; 81.347 | 1126.82 | Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E. Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation Chemical Communications, 2016, 52, 7866-7869 |
| 7119385 | CIF | C23 H20 N2 O3 | P 1 21/n 1 | 8.8491; 10.6531; 20.9154 90; 96.794; 90 | 1957.9 | Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E. Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation Chemical Communications, 2016, 52, 7866-7869 |
| 7119386 | CIF | C25 H22 N2 | I 1 2/a 1 | 18.3322; 10.0821; 20.0451 90; 90.573; 90 | 3704.7 | Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E. Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation Chemical Communications, 2016, 52, 7866-7869 |
| 7119387 | CIF | C96 H92 N12 O32 Zr6 | F m -3 m | 29.983; 29.983; 29.983 90; 90; 90 | 26954 | Naeem, Ayesha; Ting, Valeska P.; Hintermair, Ulrich; Tian, Mi; Telford, Richard; Halim, Saaiba; Nowell, Harriott; Hołyńska, Małgorzata; Teat, Simon J.; Scowen, Ian J.; Nayak, Sanjit Mixed-linker approach in designing porous zirconium-based metal‒organic frameworks with high hydrogen storage capacity Chemical Communications, 2016, 52, 7826-7829 |
| 7119388 | CIF | C96 H80 O32 Zr6 | F m -3 m | 29.941; 29.941; 29.941 90; 90; 90 | 26841 | Naeem, Ayesha; Ting, Valeska P.; Hintermair, Ulrich; Tian, Mi; Telford, Richard; Halim, Saaiba; Nowell, Harriott; Hołyńska, Małgorzata; Teat, Simon J.; Scowen, Ian J.; Nayak, Sanjit Mixed-linker approach in designing porous zirconium-based metal‒organic frameworks with high hydrogen storage capacity Chemical Communications, 2016, 52, 7826-7829 |
| 7119389 | CIF | C36 H36 Cl6 Ge3 N4 | P 1 21/c 1 | 9.4771; 16.9192; 25.2949 90; 92.298; 90 | 4052.6 | Swamy, V. S. V. S. N.; Yadav, Sandeep; Pal, Shiv; Das, Tamal; Vanka, Kumar; Sen, Sakya S. Facile access to a Ge(II) dication stabilized by isocyanides Chemical Communications, 2016, 52, 7890-7892 |
| 7119440 | CIF | C29 H36 Br F3 N O3 P | P 1 21/n 1 | 9.477; 15.308; 21.114 90; 102.525; 90 | 2990 | Ryosuke; Saijo; Hidemitsu; Uno; Shigeki; Mori; Masami; Kawase Synthesis and structures of stable phosphorus zwitterions derived from mesoionic 4_trifluoroacetyl-1,3-oxazolium-5-olates Chem.Commun., 2016, 52, 8006 |
| 7119441 | CIF | C39 H31 N O3 S | P 4/n c c | 25.9455; 25.9455; 24.2457 90; 90; 90 | 16321.5 | Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes Chem.Commun., 2016, 52, 7928 |
| 7119442 | CIF | C60 H45 N O3 S | P 4/n c c | 26.7747; 26.7747; 24.0725 90; 90; 90 | 17257.2 | Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes Chem.Commun., 2016, 52, 7928 |
| 7119443 | CIF | C62.5 H45 N O3 S | P 4/n c c | 27.3864; 27.3864; 24.2386 90; 90; 90 | 18179.3 | Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes Chem.Commun., 2016, 52, 7928 |
| 7119446 | CIF | C26 H28 F12 N6 P2 Ru | C 1 2/c 1 | 20.6432; 12.1018; 12.8802 90; 110.019; 90 | 3023.3 | Yanay; Popowski; Israel; Goldberg; Moshe; Kol The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II) Chem.Commun., 2016, 52, 7932 |
| 7119447 | CIF | C30 H32 F12 N6 P2 Ru | C 1 2 1 | 25.132; 9.8199; 17.2577 90; 131.012; 90 | 3213.8 | Yanay; Popowski; Israel; Goldberg; Moshe; Kol The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II) Chem.Commun., 2016, 52, 7932 |
| 7119448 | CIF | C24 H32 F12 N6 P2 Ru | P 31 2 1 | 10.2422; 10.2422; 24.9887 90; 90; 120 | 2270.18 | Yanay; Popowski; Israel; Goldberg; Moshe; Kol The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II) Chem.Commun., 2016, 52, 7932 |
| 7119449 | CIF | C25 H29 Cl F12 Fe N5 P2 | P 1 21 1 | 10.1753; 16.8389; 9.2498 90; 112.218; 90 | 1467.2 | Yanay; Popowski; Israel; Goldberg; Moshe; Kol The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II) Chem.Commun., 2016, 52, 7932 |
| 7119450 | CIF | C60 H74 B2 F8 N10 O20 Ru3 | P 1 21/n 1 | 14.515; 14.999; 15.692 90; 96.15; 90 | 3397 | Yuta; Tsubonouchi; Shu; Lin; Alexander; R.; Parent; Gary; W.; Brudvig; Ken; Sakai Light-induced water oxidation catalyzed by an oxido-bridged triruthenium complex with a Ru-O-Ru-O-Ru motif Chem.Commun., 2016, 52, 8018 |
| 7119451 | CIF | C60 H82 B F4 N10 O32 Ru3 S2 | P -1 | 15.229; 17.001; 17.204 65.62; 84.91; 71.63 | 3845.9 | Yuta; Tsubonouchi; Shu; Lin; Alexander; R.; Parent; Gary; W.; Brudvig; Ken; Sakai Light-induced water oxidation catalyzed by an oxido-bridged triruthenium complex with a Ru-O-Ru-O-Ru motif Chem.Commun., 2016, 52, 8018 |
| 7119454 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.5436; 14.5436; 29.1864 90; 90; 90 | 6173.4 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119455 | CIF | C36 H25 Cd N2 O4 | P 43 21 2 | 14.573; 14.573; 28.941 90; 90; 90 | 6146 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119456 | CIF | C36 H26 Cd N2 O4 | P 43 21 2 | 14.523; 14.523; 29.1177 90; 90; 90 | 6141.4 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119457 | CIF | C36 H24 Cd N2 O4 | P 43 21 2 | 14.3555; 14.3555; 29.4087 90; 90; 90 | 6060.6 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119458 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.5029; 14.5029; 29.2053 90; 90; 90 | 6142.9 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119459 | CIF | C36 H24 Cd N2 O4 | P 41 21 2 | 14.3664; 14.3664; 29.399 90; 90; 90 | 6067.8 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119460 | CIF | C36 H26 Cd N2 O4 | P 43 21 2 | 14.5318; 14.5318; 29.1429 90; 90; 90 | 6154.2 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119461 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.5128; 14.5128; 29.194 90; 90; 90 | 6148.9 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119462 | CIF | C36 H26 Cd N2 O4 | P 43 21 2 | 14.4791; 14.4791; 29.069 90; 90; 90 | 6094.2 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119463 | CIF | C36 H26 Cd N2 O4 | P 43 21 2 | 14.4739; 14.4739; 29.0695 90; 90; 90 | 6089.9 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119464 | CIF | C36 H26 Cd N2 O4 | P 43 21 2 | 14.4958; 14.4958; 29.0361 90; 90; 90 | 6101.3 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119465 | CIF | C36 H26 Cd N2 O4 | P 43 21 2 | 14.5294; 14.5294; 29.1842 90; 90; 90 | 6160.9 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119466 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.4838; 14.4838; 29.2182 90; 90; 90 | 6129.4 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119467 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.4458; 14.4458; 29.3447 90; 90; 90 | 6123.7 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119468 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.4171; 14.4171; 29.1929 90; 90; 90 | 6067.8 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119469 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.5097; 14.5097; 28.8452 90; 90; 90 | 6072.8 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119470 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.5222; 14.5222; 29.245 90; 90; 90 | 6167.6 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119471 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.5387; 14.5387; 29.246 90; 90; 90 | 6181.8 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119472 | CIF | C36 H26 Cd N2 O4 | P 43 21 2 | 14.5486; 14.5486; 29.1966 90; 90; 90 | 6179.8 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119473 | CIF | C36 H26 Cd N2 O4 | P 43 21 2 | 14.486; 14.486; 28.911 90; 90; 90 | 6066.8 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119474 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.4896; 14.4896; 29.1167 90; 90; 90 | 6113 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119475 | CIF | C36 H26 Cd N2 O4 | P 43 21 2 | 14.4789; 14.4789; 29.007 90; 90; 90 | 6081 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119476 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.5067; 14.5067; 28.888 90; 90; 90 | 6079.3 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119477 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.4975; 14.4975; 29.1189 90; 90; 90 | 6120.1 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119478 | CIF | C36 H26 Cd N2 O4 | P 43 21 2 | 14.5803; 14.5803; 29.181 90; 90; 90 | 6203.4 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119479 | CIF | C36 H26 Cd N2 O4 | P 41 21 2 | 14.5474; 14.5474; 29.2215 90; 90; 90 | 6184.1 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119480 | CIF | C36 H26 Cd N2 O4 | P 43 21 2 | 14.5616; 14.5616; 29.153 90; 90; 90 | 6181.6 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119481 | CIF | C36 H25 Cd N2 O4 | P 41 21 2 | 14.4906; 14.4906; 29.1148 90; 90; 90 | 6113.5 | Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E. Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation Chemical Communications, 2016, 52, 7990-7993 |
| 7119482 | CIF | C72 H40 In2 O16 | R -3 :H | 44.874; 44.874; 42.074 90; 90; 120 | 73373 | Panpan; Yu; Qipeng; Li; Yue; Hu; Nannan; Liu; Lijie; Zhang; Kongzhao; Su; Jinjie; Qian; Shaoming; Huang; Maochun; Hong Cuboctahedron-based indium-organic frameworks for gas sorption and selective cation exchange Chem.Commun., 2016, 52, 7978 |
| 7119483 | CIF | C25 H16 O3 | C 1 2/c 1 | 25.507; 8.1552; 16.661 90; 92.869; 90 | 3461.4 | Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation Chem.Commun., 2016, 52, 7974 |
| 7119484 | CIF | C27 H22 O4 | P -1 | 9.173; 10.382; 12.748 104.062; 94.66; 116.023 | 1033.4 | Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation Chem.Commun., 2016, 52, 7974 |
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