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Increased stability of NO and NS heterocyclic carbenes?

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dc.contributor.authorGraham, David Carlen
dc.contributor.authorYates, Brian F.en
dc.contributor.schoolSchool of Chemistry and Physicsen
dc.date.issued2004en
dc.description.abstractDensity functional theory has been used to investigate the effects of alkylation and oxidation on the stability of NO and NS heterocyclic carbenes. While O- and S-alkylation leads to a dramatic increase in stability with respect to dimerization, oxidation of the NS heterocyclic carbene to form the sulphoxide appears to have the opposite effect.en
dc.description.statementofresponsibilityDavid C. Graham and Brian F. Yatesen
dc.identifier.citationAustralian Journal of Chemistry, 2004; 57(4):359-364en
dc.identifier.doi10.1071/CH03248en
dc.identifier.issn0004-9425en
dc.identifier.urihttp://hdl.handle.net/2440/34872
dc.language.isoenen
dc.publisherCSIRO Publishingen
dc.rights© CSIRO 2004en
dc.subjectcomputational chemistry; density functional theory; heterocyclic carbenesen
dc.titleIncreased stability of NO and NS heterocyclic carbenes?en
dc.typeJournal articleen

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