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dc.contributor.authorMcGee, Karen
dc.contributor.authorTravers, Guy
dc.contributor.authorSkelton, B.
dc.contributor.authorMassi, Massimiliano
dc.contributor.authorPayne, A.
dc.contributor.authorBrown, David
dc.date.accessioned2017-01-30T13:31:21Z
dc.date.available2017-01-30T13:31:21Z
dc.date.created2012-08-07T20:00:21Z
dc.date.issued2012
dc.identifier.citationMcGee, Karen D.M. and Travers, Guy and Skelton, Brian W. and Massi, Massimiliano and Payne, Alan D. and Brown, David H. 2012. Synthesis, Solid-state Structures, Solution Behaviour and Catalysis Studies of Nickel Complexes of Bis(benzimidazolin-2-ylidene)pyridine Pincer Ligands. Australian Journal of Chemistry. 65 (7): pp. 823-833.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/32525
dc.identifier.doi10.1071/CH12044
dc.description.abstract

N-Heterocyclic carbene–nickel complexes with five- and four-coordinate geometries [(CNC)NiBr2] and [(CNC)NiBr]X (X = PF6 or BPh4) have been prepared with the pincer ligands 2,6-bis(N-octylbenzimidazolin-2-ylidene)pyridine and 2,6-bis(N-butyl-5,6-dimethoxybenzimidazolin-2-ylidene)pyridine. The addition of the n-octyl substituent significantly extends the solubility of the complexes and has allowed UV-vis solution studies of the complexes in dichloromethane and methanol. The four- and five-coordinate species exist in equilibrium in solution and this equilibrium has been explored by UV-vis studies. The complexes have also been characterized by NMR studies, and single crystal X-ray diffraction studies have been performed on [(CNC)NiBr2] (where CNC = 2,6-bis(N-octylbenzimidazolin-2-ylidene)pyridine) and [(CNC)NiBr]BPh4 (where CNC = 2,6-bis(N-butyl-5,6-dimethoxybenzimidazolin-2-ylidene)pyridine).

dc.publisherCSIRO Publishing
dc.titleSynthesis, Solid-state Structures, Solution Behaviour and Catalysis Studies of Nickel Complexes of Bis(benzimidazolin-2-ylidene)pyridine Pincer Ligands
dc.typeJournal Article
dcterms.source.volume65
dcterms.source.startPage823
dcterms.source.endPage833
dcterms.source.issn00049425
dcterms.source.titleAustralian Journal of Chemistry
curtin.note

Copyright © 2012 CSIRO

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curtin.accessStatusOpen access


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