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Conference Paper: Structures and suzuki-coupling of N-heterocyclic carbene complexes of PdII with coordinated solvent and PPh3

TitleStructures and suzuki-coupling of N-heterocyclic carbene complexes of PdII with coordinated solvent and PPh3
Authors
Issue Date2009
Citation
Australian Journal of Chemistry, 2009, v. 62, n. 9, p. 1047-1053 How to Cite?
AbstractA series of mononuclear N,N-heterocyclic carbene (NNHC) complexes of PdII with mixed ligands of 1,3-dibenzylbenzimidazoly-2-ylidene and solvate (dimethyl sulfoxide, CH3CN, N,N-dimethylformamide, and pyridine) or PPh3 were prepared and characterized by X-ray single-crystal diffraction analysis. They are more active in the SuzukiMiyaura coupling of selected aryl bromides than their N,S-heterocyclic carbene (NSHC) analogues. © CSIRO 2009.
Persistent Identifierhttp://hdl.handle.net/10722/219605
ISSN
2015 Impact Factor: 1.427
2015 SCImago Journal Rankings: 0.548

 

DC FieldValueLanguage
dc.contributor.authorYen, Swee Kuan-
dc.contributor.authorKoh, Lip Lin-
dc.contributor.authorHuynh, Han Vinh-
dc.contributor.authorHor, T. S Andy-
dc.date.accessioned2015-09-23T02:57:30Z-
dc.date.available2015-09-23T02:57:30Z-
dc.date.issued2009-
dc.identifier.citationAustralian Journal of Chemistry, 2009, v. 62, n. 9, p. 1047-1053-
dc.identifier.issn0004-9425-
dc.identifier.urihttp://hdl.handle.net/10722/219605-
dc.description.abstractA series of mononuclear N,N-heterocyclic carbene (NNHC) complexes of PdII with mixed ligands of 1,3-dibenzylbenzimidazoly-2-ylidene and solvate (dimethyl sulfoxide, CH3CN, N,N-dimethylformamide, and pyridine) or PPh3 were prepared and characterized by X-ray single-crystal diffraction analysis. They are more active in the SuzukiMiyaura coupling of selected aryl bromides than their N,S-heterocyclic carbene (NSHC) analogues. © CSIRO 2009.-
dc.languageeng-
dc.relation.ispartofAustralian Journal of Chemistry-
dc.titleStructures and suzuki-coupling of N-heterocyclic carbene complexes of PdII with coordinated solvent and PPh3-
dc.typeConference_Paper-
dc.description.natureLink_to_subscribed_fulltext-
dc.identifier.doi10.1071/CH09196-
dc.identifier.scopuseid_2-s2.0-70349334157-
dc.identifier.volume62-
dc.identifier.issue9-
dc.identifier.spage1047-
dc.identifier.epage1053-

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