# Search results of SQL query from the Crystallography Open Database # Date and time performed: 2024-12-01T00:36:16+01:00 # Query: # SELECT data.* # FROM # data JOIN jaltnames # ON altname = journal # WHERE # (status is null or status != 'retracted') and # (journal_id IN (SELECT DISTINCT(journal_id) FROM jaltnames WHERE altname LIKE 'Catal. Sci. Technol.') AND volume = 2 AND duplicateof IS NULL AND (status is NULL OR status != 'errors') AND (method is NULL OR method != 'theoretical')) # ORDER BY file asc file,a,siga,b,sigb,c,sigc,alpha,sigalpha,beta,sigbeta,gamma,siggamma,vol,sigvol,celltemp,sigcelltemp,diffrtemp,sigdiffrtemp,cellpressure,sigcellpressure,diffrpressure,sigdiffrpressure,thermalhist,pressurehist,compoundsource,nel,sg,sgHall,sgNumber,commonname,chemname,mineral,formula,calcformula,cellformula,Z,Zprime,acce_code,authors,title,journal,year,volume,issue,firstpage,lastpage,doi,method,radiation,wavelength,radType,radSymbol,Rall,Robs,Rref,wRall,wRobs,wRref,RFsqd,RI,gofall,gofobs,gofgt,gofref,duplicateof,optimal,status,flags,svnrevision,date,time,onhold "1556286","11.5434","0.0011","14.8956","0.0015","15.1659","0.0015","62.313","0.001","86.134","0.001","78.115","0.001","2258.4","0.4","173","2","173","2","","","","","","","","6","P -1","-P 1","2","","","","- C54.2 H48.4 Cl0.4 N2 O P2 -","- C54.2 H48.4 Cl0.4 N2 O P2 -","- C108.4 H96.8 Cl0.8 N4 O2 P4 -","2","1","","Wheaton, Craig A.; Hayes, Paul G.","Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes","Catal. Sci. Technol.","2012","2","1","125","","10.1039/C1CY00306B","","","0.71073","MoKα","","0.1432","0.0646","","","0.1472","0.1827","","","","","","1.11","","","","has coordinates","244148","2020-10-21","18:00:00","" "1556287","18.0198","0.0009","14.0045","0.0007","16.7584","0.0009","90","","109.646","0.001","90","","3982.9","0.4","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C50 H40 N2 O P2 -","- C50 H40 N2 O P2 -","- C200 H160 N8 O4 P8 -","4","1","","Wheaton, Craig A.; Hayes, Paul G.","Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes","Catal. Sci. Technol.","2012","2","1","125","","10.1039/C1CY00306B","","","0.71073","MoKα","","0.0465","0.0394","","","0.1041","0.1079","","","","","","1.081","","","","has coordinates","244148","2020-10-21","18:00:00","" "1556288","9.373","0.011","13.769","0.017","17.95","0.02","104.285","0.015","90.99","0.014","92.535","0.015","2242","5","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C51 H39 N2 O P2 -","- C51 H39 N2 O P2 -","- C102 H78 N4 O2 P4 -","2","1","","Wheaton, Craig A.; Hayes, Paul G.","Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes","Catal. Sci. Technol.","2012","2","1","125","","10.1039/C1CY00306B","","","0.71073","MoKα","","0.178","0.0794","","","0.1825","0.2141","","","","","","0.915","","","","has coordinates","244148","2020-10-21","18:00:00","" "1556289","14.3702","0.0007","15.2542","0.0007","17.2588","0.0008","81.451","0.001","66.469","0.001","76.867","0.001","3370.8","0.3","173","2","173","2","","","","","","","","7","P -1","-P 1","2","","","","- C85 H77 B N2 O P2 Zn -","- C85 H77 B N2 O P2 Zn -","- C170 H154 B2 N4 O2 P4 Zn2 -","2","1","","Wheaton, Craig A.; Hayes, Paul G.","Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes","Catal. Sci. Technol.","2012","2","1","125","","10.1039/C1CY00306B","","","0.71073","MoKα","","0.037","0.0302","","","0.0785","0.0825","","","","","","1.016","","","","has coordinates","244148","2020-10-21","18:00:00","" "1556290","9.9214","0.0008","17.1175","0.0013","18.4747","0.0014","86.754","0.001","78.725","0.001","80.859","0.001","3036.9","0.4","173","2","173","2","","","","","","","","7","P -1","-P 1","2","","","","- C76.18 H63.47 B N2 O P2 Zn -","- C76.2 H63.48 B N2 O P2 Zn -","- C152.4 H126.96 B2 N4 O2 P4 Zn2 -","2","1","","Wheaton, Craig A.; Hayes, Paul G.","Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes","Catal. Sci. Technol.","2012","2","1","125","","10.1039/C1CY00306B","","","0.71073","MoKα","","0.0878","0.0445","","","0.0849","0.0987","","","","","","1.012","","","","has coordinates,has disorder","244148","2020-10-21","18:00:00","" "1556291","9.9023","0.0005","16.867","0.0009","20.7112","0.0011","101.974","0.001","91.114","0.001","95.296","0.001","3366.9","0.3","173","2","173","2","","","","","","","","7","P -1","-P 1","2","","","","- C80.65 H63.86 B N2 O P2 Zn -","- C80.65 H63.86 B N2 O P2 Zn -","- C161.3 H127.72 B2 N4 O2 P4 Zn2 -","2","1","","Wheaton, Craig A.; Hayes, Paul G.","Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes","Catal. Sci. Technol.","2012","2","1","125","","10.1039/C1CY00306B","","","0.71073","MoKα","","0.0465","0.0387","","","0.1026","0.1073","","","","","","1.069","","","","has coordinates,has disorder","244148","2020-10-21","18:00:00","" "1556292","11.4655","0.0017","19.564","0.003","19.662","0.003","99.64","0.002","103.416","0.002","92.916","0.002","4210.9","1.1","173","2","173","2","","","","","","","","9","P -1","-P 1","2","","","","- C86.83 H60.66 B Cl1.66 F24 N2 O4 P2 Zn -","- C86.83 H60.66 B Cl1.66 F24 N2 O4 P2 Zn -","- C173.66 H121.32 B2 Cl3.32 F48 N4 O8 P4 Zn2 -","2","1","","Wheaton, Craig A.; Hayes, Paul G.","Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes","Catal. Sci. Technol.","2012","2","1","125","","10.1039/C1CY00306B","","","0.71073","MoKα","","0.1704","0.0785","","","0.1742","0.2148","","","","","","1.02","","","","has coordinates,has disorder","244148","2020-10-21","18:00:00","" "1556293","18.781","0.0011","27.1179","0.0016","18.6506","0.0011","90","","116.785","0.001","90","","8479.6","0.9","173","2","173","2","","","","","","","","9","P 1 21/c 1","-P 2ybc","14","","","","- C90 H60 B Br0.38 F24 N2 O4 P2 Zn -","- C90 H60 B Br0.38 F24 N2 O4 P2 Zn -","- C360 H240 B4 Br1.52 F96 N8 O16 P8 Zn4 -","4","1","","Wheaton, Craig A.; Hayes, Paul G.","Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes","Catal. Sci. Technol.","2012","2","1","125","","10.1039/C1CY00306B","","","0.71073","MoKα","","0.0797","0.0613","","","0.1516","0.1617","","","","","","1.117","","","","has coordinates,has disorder","244148","2020-10-21","18:00:00","" "1556294","10.378","0.002","16.008","0.003","31.765","0.006","90","","95.61","0.03","90","","5251.9","1.7","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C57 H50 Br2 N2 Ni -","- C57 H50 Br2 N2 Ni -","- C228 H200 Br8 N8 Ni4 -","4","1","","Liu, Hao; Zhao, Weizhen; Yu, Jiangang; Yang, Wenhong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua","Synthesis, characterization and ethylenepolymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands","Catal. Sci. Technol.","2012","2","2","415","","10.1039/C1CY00319D","","","0.71073","MoKα","","0.0886","0.0696","","","0.1778","0.1894","","","","","","1.175","","","","has coordinates","244149","2020-10-21","18:00:00","" "1556295","15.352","0.003","22.551","0.005","15.38","0.003","90","","106.96","0.03","90","","5093","2","173","2","173","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C56 H48 Br2 N2 Ni -","- C56 H48 Br2 N2 Ni -","- C224 H192 Br8 N8 Ni4 -","4","1","","Liu, Hao; Zhao, Weizhen; Yu, Jiangang; Yang, Wenhong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua","Synthesis, characterization and ethylenepolymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands","Catal. Sci. Technol.","2012","2","2","415","","10.1039/C1CY00319D","","","0.71073","MoKα","","0.0937","0.0683","","","0.1528","0.1664","","","","","","1.105","","","","has coordinates","244149","2020-10-21","18:00:00","" "1556296","15.33","0.003","22.285","0.005","14.954","0.003","90","","106.33","0.03","90","","4902.6","1.9","173","2","173","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C54 H44 Cl2 N2 Ni O0 -","- C54 H44 Cl2 N2 Ni -","- C216 H176 Cl8 N8 Ni4 -","4","1","","Liu, Hao; Zhao, Weizhen; Yu, Jiangang; Yang, Wenhong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua","Synthesis, characterization and ethylenepolymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands","Catal. Sci. Technol.","2012","2","2","415","","10.1039/C1CY00319D","","","0.71073","MoKα","","0.1619","0.1173","","","0.278","0.3059","","","","","","1.155","","","","has coordinates","244149","2020-10-21","18:00:00","" "1556297","15.492","0.008","17.191","0.01","25.784","0.01","90","","90","","90","","6867","6","293","2","293","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C28 H33 Cl4 Co N3 O2 -","- C28 H33 Cl4 Co N3 O2 -","- C224 H264 Cl32 Co8 N24 O16 -","8","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","1.54178","CuKα","","0.3039","0.0972","","","0.201","0.2764","","","","","","0.85","","","","has coordinates,has disorder","244205","2020-10-21","18:00:00","" "1556298","23.2849","0.0008","16.2809","0.0004","17.6654","0.0005","90","","106.957","0.003","90","","6405.8","0.3","293","","293","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C28 H33 Cl4 Fe N3 S2 -","- C28 H33 Cl4 Fe N3 S2 -","- C224 H264 Cl32 Fe8 N24 S16 -","8","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","1.54178","CuKα","","0.0892","0.0539","","0.1494","","0.1265","","","1.027","","","1.103","","","","has coordinates,has disorder","244205","2020-10-21","18:00:00","" "1556299","16.114","0.002","8.9394","0.0007","27.383","0.004","90","","99.828","0.014","90","","3886.6","0.8","293","","293","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C41 H43 Cl2 Fe N3 O3 -","- C41 H43 Cl2 Fe N3 O3 -","- C164 H172 Cl8 Fe4 N12 O12 -","4","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","1.54178","CuKα","","0.1164","0.0586","","0.1604","","0.1274","","","1.041","","","1.146","","","","has coordinates","244205","2020-10-21","18:00:00","" "1556300","17.148","0.004","20.564","0.004","22.319","0.004","90","","90","","90","","7870","3","293","","293","","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C38 H37 Cl4 Fe N3 S2 -","- C38 H37 Cl4 Fe N3 S2 -","- C304 H296 Cl32 Fe8 N24 S16 -","8","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","0.71073","MoKα","","0.1875","0.075","","","0.1522","0.1874","","","","","","0.926","","","","has coordinates,has disorder","244205","2020-10-21","18:00:00","" "1556301","12.3896","0.0016","19.617","0.002","16.797","0.002","90","","95.449","0.016","90","","4064","0.8","203","","203","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C38.5 H38 Cl6 N3 S2 V -","- C38.5 H38 Cl6 N3 S2 V -","- C154 H152 Cl24 N12 S8 V4 -","4","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","0.71073","MoKα","","0.0976","0.0545","","","0.1164","0.1297","","","","","","0.987","","","","has coordinates,has disorder","244205","2020-10-21","18:00:00","" "1556302","12.3561","0.0014","19.623","0.002","16.75","0.002","90","","95.756","0.015","90","","4040.8","0.8","203","","203","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C38.5 H38 Cl6 Cr N3 S2 -","- C38.5 H38 Cl6 Cr N3 S2 -","- C154 H152 Cl24 Cr4 N12 S8 -","4","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","0.71073","MoKα","","0.0648","0.0416","","","0.0966","0.1051","","","","","","1.02","","","","has coordinates,has disorder","244205","2020-10-21","18:00:00","" "1556303","17.056","0.003","20.693","0.007","22.231","0.004","90","","90","","90","","7846","3","203","","203","","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C38 H37 Cl4 Mn N3 S2 -","- C38 H37 Cl4 Mn N3 S2 -","- C304 H296 Cl32 Mn8 N24 S16 -","8","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","0.71073","MoKα","","0.1762","0.0746","","","0.1239","0.1495","","","","","","0.925","","","","has coordinates,has disorder","244205","2020-10-21","18:00:00","" "1556304","17.54","0.003","20.405","0.004","22.23","0.004","90","","90","","90","","7956","3","203","","203","","","","","","","","","7","P b c a","-P 2ac 2ab","61","","","","- C41 H43 Br2 N3 Ni O S2 -","- C41 H43 Br2 N3 Ni O S2 -","- C328 H344 Br16 N24 Ni8 O8 S16 -","8","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","0.71073","MoKα","","0.1832","0.0786","","","0.1878","0.2168","","","","","","1.049","","","","has coordinates","244205","2020-10-21","18:00:00","" "1556305","9.2178","0.0011","29.17","0.002","16.7749","0.0011","90","","92.674","0.007","90","","4505.6","0.7","183","","183","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C44.5 H50 Cl5 Fe N3 O2 -","- C44.5 H50 Cl5 Fe N3 O2 -","- C178 H200 Cl20 Fe4 N12 O8 -","4","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","1.54178","CuKα","","0.0899","0.0562","","0.1567","0.1323","","","","1.029","","","1.085","","","","has coordinates,has disorder","244205","2020-10-21","18:00:00","" "1556306","12.8687","0.0006","19.6515","0.0016","18.0924","0.0009","90","","90.931","0.004","90","","4574.8","0.5","183","","183","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C44.25 H49.5 Cl4.5 Co N3 O2 -","- C44.25 H49.5 Cl4.5 Co N3 O2 -","- C177 H198 Cl18 Co4 N12 O8 -","4","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","1.54178","CuKα","","0.106","0.0615","","","0.1421","0.1587","","","","","","1.008","","","","has coordinates,has disorder","244205","2020-10-21","18:00:00","" "1556307","34.005","0.003","10.0092","0.0011","27.105","0.003","90","","94.482","0.007","90","","9197.3","1.7","183","","183","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C44.5 H50 Cl5 Fe N3 S2 -","- C44.5 H50 Cl5 Fe N3 S2 -","- C356 H400 Cl40 Fe8 N24 S16 -","8","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","1.54178","CuKα","","0.1005","0.0594","","","0.1282","0.1417","","","","","","1.029","","","","has coordinates,has disorder","244205","2020-10-21","18:00:00","" "1556308","34.234","0.006","10.0665","0.001","27.315","0.004","90","","93.888","0.012","90","","9392","2","293","","293","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C44.5 H50 Cl5 Co N3 S2 -","- C44.5 H50 Cl5 Co N3 S2 -","- C356 H400 Cl40 Co8 N24 S16 -","8","1","","Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J.","The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series","Catalysis Science & Technology","2012","2","3","643","","10.1039/c2cy00448h","","","0.71073","MoKα","","0.0878","0.0494","","","0.1171","0.1321","","","","","","1.005","","","","has coordinates,has disorder","244205","2020-10-21","18:00:00","" "1556309","7.8175","0.0016","16.296","0.003","16.654","0.003","100.4","0.03","100.58","0.03","102.97","0.03","1977.2","0.8","93","2","93","2","","","","","","","","6","P -1","-P 1","2","","","","- C19 H26 Cl O3 P Pd -","- C19 H26 Cl O3 P Pd -","- C76 H104 Cl4 O12 P4 Pd4 -","4","2","","Fuentes, José A.; Slawin, Alexandra M. Z.; Clarke, Matthew L.","Application of palladium (trioxo-adamantyl cage phosphine)chloride complexes as catalysts for the alkoxycarbonylation of styrene; Pd catalysed tert-butoxycarbonylation of styrene","Catalysis Science & Technology","2012","2","4","715","","10.1039/c2cy00521b","","","0.71073","MoKα","","0.0798","0.0594","","","0.1431","0.1561","","","","","","1.164","","","","has coordinates","244206","2020-10-21","18:00:00","" "1556310","9.552","0.003","15.094","0.004","16.038","0.004","90","","100.126","0.007","90","","2276.3","1.1","93","2","93","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C22 H32 Cl O4 P Pd -","- C22 H32 Cl O4 P Pd -","- C88 H128 Cl4 O16 P4 Pd4 -","4","1","","Fuentes, José A.; Slawin, Alexandra M. Z.; Clarke, Matthew L.","Application of palladium (trioxo-adamantyl cage phosphine)chloride complexes as catalysts for the alkoxycarbonylation of styrene; Pd catalysed tert-butoxycarbonylation of styrene","Catalysis Science & Technology","2012","2","4","715","","10.1039/c2cy00521b","","","0.71073","MoKα","","0.0455","0.0411","","","0.0954","0.0981","","","","","","1.1","","","","has coordinates","244206","2020-10-21","18:00:00","" "1556311","8.301","0.003","10.979","0.004","11.71","0.003","80.225","0.012","85.04","0.03","89.69","0.02","1047.7","0.6","173","2","173","2","","","","","","","","5","P -1","-P 1","2","","","","- C18 H18 F12 N2 O2 -","- C18 H18 F12 N2 O2 -","- C36 H36 F24 N4 O4 -","2","1","","Legros, Julien; Bonnet-Delpon, Danièle; Crousse, Benoit; Slawin, Alexandra M. Z.","Self-assembly between 1,4-diazabicyclo[2.2.2]octane and bis(hexafluoroalcohols): solid/liquid phase switching for catalyst recycling","Catalysis Science & Technology","2012","2","5","934","","10.1039/c2cy00528j","","","1.54178","CuKα","","0.07","0.059","","","0.1634","0.177","","","","","","1.088","","","","has coordinates","244207","2020-10-21","18:00:00","" "1556312","25.06","0.02","6.782","0.005","13.057","0.015","90","","110.81","0.03","90","","2074","3","173","2","173","2","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C18 H18 F12 N2 O2 -","- C18 H18 F12 N2 O2 -","- C72 H72 F48 N8 O8 -","4","1","","Legros, Julien; Bonnet-Delpon, Danièle; Crousse, Benoit; Slawin, Alexandra M. Z.","Self-assembly between 1,4-diazabicyclo[2.2.2]octane and bis(hexafluoroalcohols): solid/liquid phase switching for catalyst recycling","Catalysis Science & Technology","2012","2","5","934","","10.1039/c2cy00528j","","","1.54178","CuKα","","0.1404","0.1324","","","0.3253","0.3567","","","","","","1.33","","","","has coordinates","244207","2020-10-21","18:00:00","" "1556313","7.724","0.005","13.385","0.005","14","0.005","68.935","0.005","83.939","0.005","89.447","0.005","1342.5","1.1","294","2","294","2","","","","","","","","7","P -1","-P 1","2","","","","- C25 H24 Br N3 O5 Pd S -","- C23 H20 Br N3 O3 Pd S -","- C46 H40 Br2 N6 O6 Pd2 S2 -","2","1","","Srinivas, Keesara; Srinivas, Pottabathula; Prathima, Parvathaneni Sai; Balaswamy, Kodicherla; Sridhar, Balsubramanian; Rao, Mandapati Mohan","Thiopseudourea ligated palladium complexes: synthesis, characterization and application as catalysts for Suzuki‒Miyaura, Sonogashira, Heck and Hiyama reactions","Catalysis Science & Technology","2012","2","6","1180","","10.1039/c2cy00542e","","x-ray","0.71073","MoKα","","0.0298","0.0278","","","0.0767","0.0784","","","","","","1.077","","","","has coordinates","244208","2020-10-21","18:00:00","" "1556314","10.515","0.002","13.887","0.003","15.272","0.003","80.61","0.03","71.05","0.03","70.1","0.03","1979.8","0.8","173","2","173","2","","","","","","","","6","P -1","-P 1","2","","","","- C90 H84 Br0 N2 Ni O2 -","- C90 H84 N2 Ni O2 -","- C90 H84 N2 Ni O2 -","1","0.5","","Zhou, Zihong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua","Nickel bis{4,6-dibenzhydryl-2-[(arylimino)methyl]phenoxylate} complexes: Synthesis, structures, and catalytic behaviour towards ethylene and norbornene","Catalysis Science & Technology","2012","2","7","1340","","10.1039/c2cy20028g","","","0.71073","MoKα","","","0.0787","","","0.2086","0.2206","","","","","","1.144","","","","has coordinates","244209","2020-10-21","18:00:00","" "1556315","47.225","0.009","16.333","0.003","17.278","0.004","90","","110.26","0.03","90","","12502","5","173","2","173","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C78 H56 F4 N2 Ni O2 -","- C78 H56 F4 N2 Ni O2 -","- C624 H448 F32 N16 Ni8 O16 -","8","1","","Zhou, Zihong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua","Nickel bis{4,6-dibenzhydryl-2-[(arylimino)methyl]phenoxylate} complexes: Synthesis, structures, and catalytic behaviour towards ethylene and norbornene","Catalysis Science & Technology","2012","2","7","1340","","10.1039/c2cy20028g","","","0.71073","MoKα","","","0.0974","","","0.2313","0.2436","","","","","","1.175","","","","has coordinates","244209","2020-10-21","18:00:00","" "1556316","8.8191","0.0006","17.5507","0.0011","20.7531","0.0013","90","","90","","90","","3212.2","0.4","293","2","293","2","","","","","","","","4","P c a b","-P 2bc 2ac","61","","","","- C17 H17 N O5 -","- C17 H17 N O5 -","- C136 H136 N8 O40 -","8","1","","Ananthakrishnan, Rajakumar; Gazi, Sarifuddin","[Ru(bpy)3]2+ aided photocatalytic synthesis of 2-arylpyridines via Hantzsch reaction under visible irradiation and oxygen atmosphere","Catalysis Science & Technology","2012","2","7","1463","","10.1039/c2cy20050c","","","0.71073","MoKα","","0.0788","0.052","","","0.1416","0.1682","","","","","","1.053","","","","has coordinates","244210","2020-10-21","18:00:00","" "1556317","10.9698","0.0005","12.9718","0.0006","13.3427","0.0007","91.834","0.003","104.278","0.003","92.66","0.003","1836.16","0.16","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C40 H54 N2 O3 Zn -","- C40 H54 N2 O3 Zn -","- C80 H108 N4 O6 Zn2 -","2","1","","Taherimehr, Masoumeh; Decortes, Antonello; Al-Amsyar, Syed M.; Lueangchaichaweng, Warunee; Whiteoak, Christopher J.; Escudero-Adán, Eduardo C.; Kleij, Arjan W.; Pescarmona, Paolo P.","A highly active Zn(salphen) catalyst for production of organic carbonates in a green CO2 medium","Catalysis Science & Technology","2012","2","11","2231","","10.1039/c2cy20171b","","","0.71073","MoKα","","0.0597","0.0431","","","0.1182","0.1279","","","","","","1.043","","","","has coordinates,has disorder","244211","2020-10-21","18:00:00","" "1556318","42.19","","9.719","","31.932","","90","","110.08","","90","","12297.6","","100","2","100","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C68.5 H85 N4 O9 Zn2 -","- C68.5 H85 N4 O9 Zn2 -","- C548 H680 N32 O72 Zn16 -","8","1","","Taherimehr, Masoumeh; Decortes, Antonello; Al-Amsyar, Syed M.; Lueangchaichaweng, Warunee; Whiteoak, Christopher J.; Escudero-Adán, Eduardo C.; Kleij, Arjan W.; Pescarmona, Paolo P.","A highly active Zn(salphen) catalyst for production of organic carbonates in a green CO2 medium","Catalysis Science & Technology","2012","2","11","2231","","10.1039/c2cy20171b","","","0.71073","MoKα","","0.063","0.0393","","","0.0984","0.112","","","","","","1.024","","","","has coordinates,has disorder","244211","2020-10-21","18:00:00","" "1556319","17.529","0.004","18.752","0.004","25.656","0.005","90","","90","","90","","8433","3","173","2","173","2","","","","","","","","6","P b c a","-P 2ac 2ab","61","","","","- C48 H38 Cl2 N2 O Ti -","- C48 H38 Cl2 N2 O Ti -","- C384 H304 Cl16 N16 O8 Ti8 -","8","1","","Huang, Wei; Zhang, Wenjuan; Sun, Wen-Hua; Wang, Lin; Redshaw, Carl","Synthesis, characterization, and the ethylene (co-)polymerization behaviour of half-titanocene dichloride 2-aryliminoquinolin-8-olates","Catalysis Science & Technology","2012","2","10","2090","","10.1039/c2cy20240a","","","0.71073","MoKα","","0.1428","0.1065","","","0.2577","0.2817","","","","","","1.153","","","","has coordinates","244212","2020-10-21","18:00:00","" "1556320","53.675","0.011","10.021","0.002","24.886","0.005","90","","100.29","0.03","90","","13170","5","173","2","173","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C37 H32 Cl2 N2 O Ti -","- C37 H32 Cl2 N2 O Ti -","- C592 H512 Cl32 N32 O16 Ti16 -","16","2","","Huang, Wei; Zhang, Wenjuan; Sun, Wen-Hua; Wang, Lin; Redshaw, Carl","Synthesis, characterization, and the ethylene (co-)polymerization behaviour of half-titanocene dichloride 2-aryliminoquinolin-8-olates","Catalysis Science & Technology","2012","2","10","2090","","10.1039/c2cy20240a","","","0.71073","MoKα","","","0.0932","","","0.2446","0.2632","","","","","","1.069","","","","has coordinates","244212","2020-10-21","18:00:00","" "1556321","18.108","0.001","9.5124","0.0005","18.3546","0.0012","90","","113.59","0.008","90","","2897.4","0.3","100","2","100.15","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C12 H12 Au Cl3 N2 -","- C12 H12 Au Cl3 N2 -","- C96 H96 Au8 Cl24 N16 -","8","2","","O'Neill, James A. T.; Rosair, Georgina M.; Lee, Ai-Lan","Gold(iii)–oxo complexes as catalysts in intramolecular hydroamination","Catalysis Science & Technology","2012","2","9","1818","","10.1039/c2cy20255g","","","0.710747","Molybdenum","","0.0199","0.0175","","","0.0437","0.0447","","","","","","1.044","","","","has coordinates","275434","2022-05-16","05:31:58","" "1556322","22.1175","0.001","14.791","0.0007","9.5257","0.0004","90","","99.676","0.002","90","","3071.9","0.2","100","2","100","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C12 H13 Au Cl4 N2 -","- C12 H13 Au Cl4 N2 -","- C96 H104 Au8 Cl32 N16 -","8","1","","O'Neill, James A. T.; Rosair, Georgina M.; Lee, Ai-Lan","Gold(iii)‒oxo complexes as catalysts in intramolecular hydroamination","Catalysis Science & Technology","2012","2","9","1818","","10.1039/c2cy20255g","","","0.71073","MoKα","","0.0356","0.0275","","","0.0615","0.0649","","","","","","1.016","","","","has coordinates","244213","2020-10-21","18:00:00","" "1556323","7.6032","0.0006","9.2289","0.0008","9.96","0.0009","82.321","0.005","85.907","0.005","88.085","0.005","690.65","0.1","200","2","200.15","","","","","","","","","6","P -1","-P 1","2","","","","- C12 H12 Au Cl N2 O5 -","- C12 H12 Au Cl N2 O5 -","- C24 H24 Au2 Cl2 N4 O10 -","2","1","","O'Neill, James A. T.; Rosair, Georgina M.; Lee, Ai-Lan","Gold(iii)‒oxo complexes as catalysts in intramolecular hydroamination","Catalysis Science & Technology","2012","2","9","1818","","10.1039/c2cy20255g","","","0.71073","MoKα","","0.0821","0.0724","","","0.1982","0.2089","","","","","","1.063","","","","has coordinates","244213","2020-10-21","18:00:00","" "1556324","20.5265","0.0009","13.4139","0.0009","29.7267","0.0015","90","","91.812","0.002","90","","8180.9","0.8","116","2","100","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C40 H54 Cl4 N2 O3 Ru -","- C40 H54 Cl4 N2 O3 Ru -","- C320 H432 Cl32 N16 O24 Ru8 -","8","2","","Leitgeb, Anita; Abbas, Mudassar; Fischer, Roland C.; Poater, Albert; Cavallo, Luigi; Slugovc, Christian","A latent ruthenium based olefin metathesis catalyst with a sterically demanding NHC ligand","Catalysis Science & Technology","2012","2","8","1640","","10.1039/c2cy20311a","","x-ray","0.71073","MoKα","","0.0468","0.0284","","","0.0608","0.0706","","","","","","1.029","","","","has coordinates","244214","2020-10-21","18:00:00",""