Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/19521
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dc.contributor.authorPattanayak, Poulamipt
dc.contributor.authorPratihar, Jahar Lalpt
dc.contributor.authorPatra, Debprasadpt
dc.contributor.authorBrandao, Paulapt
dc.contributor.authorFelix, Vitorpt
dc.contributor.authorChattopadhyay, Surajitpt
dc.date.accessioned2017-12-07T19:15:34Z-
dc.date.issued2014pt
dc.identifier.issn0277-5387pt
dc.identifier.urihttp://hdl.handle.net/10773/19521-
dc.description.abstractThe reaction of the multidentate ligand N-(2-(aryldiazenyl)phenyl)picolinamide, HL (3a, 3b and 3c) [HL is ArN = NC6H4NHC(O)Py, where Ar is C6H5 for HL1 (3a), p-MeC6H4 for HL2 (3b) or p-ClC6H4 for HL3 (3c), and Py stands for pyridyl], with Cu(CH3COO)(2)center dot H2O and Na2PdCl4 separately afforded the complexes [(L)(2)Cu] (4a, 4b and 4c) and [(L)PdCl] (5a, 5b and 5c) respectively, where the deprotonated ligand L- binds copper(II) and palladium(II) in a tridentate (N,N,N) fashion. X-ray structures of [(L-3)(2)Cu] (4c) and [(L-1)PdCl] (5a) were determined to confirm the molecular structures. The newly synthesized complex 4a exhibits catalytic activity toward the oxidation of alcohols to the corresponding carbonyl compounds and oxidation of organic thioethers to sulfoxide and sulfone, whereas the complex 5a is an active catalyst for Suzuki and Heck reactions. (C) 2014 Elsevier Ltd. All rights reserved.pt
dc.language.isoengpt
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDpt
dc.relationinfo:eu-repo/grantAgreement/FCT/COMPETE/132936/PTpt
dc.rightsrestrictedAccesspor
dc.subjectCROSS-COUPLING REACTIONSpt
dc.subjectLIQUID-PHASE OXIDATIONpt
dc.subjectTERMINAL ALKYNESpt
dc.subjectARYL BROMIDESpt
dc.subjectDIAZOKETIMINATO COMPLEXESpt
dc.subjectSONOGASHIRA REACTIONpt
dc.subjectCATALYZED OXIDATIONpt
dc.subjectBENZYLIC ALCOHOLSpt
dc.subjectHYDROGEN-PEROXIDEpt
dc.subjectAEROBIC OXIDATIONpt
dc.titleSynthesis, characterization, structure and properties of copper and palladium complexes incorporating azo-amide ligandspt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage43pt
degois.publication.lastPage51pt
degois.publication.titlePOLYHEDRONpt
degois.publication.volume79pt
dc.date.embargo10000-01-01-
dc.relation.publisherversion10.1016/j.poly.2014.03.053pt
dc.identifier.doi10.1016/j.poly.2014.03.053pt
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