Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4677
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dc.contributor.authorBruce, M.-
dc.contributor.authorHall, B.-
dc.contributor.authorZaitseva, N.-
dc.contributor.authorSkelton, B.-
dc.contributor.authorWhite, A.-
dc.date.issued1998-
dc.identifier.citationJournal- Chemical Society Dalton Transactions, 1998; (11):1793-1803-
dc.identifier.issn0300-9246-
dc.identifier.issn1364-5447-
dc.identifier.urihttp://hdl.handle.net/2440/4677-
dc.description.abstractA synthesis of neutral vinylideneruthenium complexes [RuCl(CCHR)(PPh3)(-C5Me5)] (R = Ph, But or SiMe3) from [RuCl(PPh3)2(-C5Me5)] and 1-alkynes has been developed. This takes advantage of the presence of two bulky ligands (PPh3 and C5Me5), which results in displacement of one PPh3 ligand (rather than chloride) and concomitant isomerisation of the 1-alkyne to vinylidene ligands. The vinylidene complexes undergo facile loss of HCl on treatment with NaOMe in the presence of a 2e donor ligand (L) to give the neutral acetylide complexes [Ru(CCR)L(PPh3)(-C5Me5)] [R = Ph, L = PPh3, CO, O2 or dppm-P; R = But, L = PPh3, CO, C2H4, dppe-P, C2(PPh2)2-P, S2, P(OMe)3 or AsPh3]; the complexes [Ru(CCBut)(L2)(-C5Me5)] [L2 = dppm or PPh2CH CHPPh2] and [Ru(S2CCCBut)(PPh3)(-C5Me5)] were also obtained. Crystal structure determinations were carried out on eleven of the complexes.-
dc.description.statementofresponsibilityMichael I. Bruce, Ben C. Hall, Natasha N. Zaitseva, Brian W. Skelton and Allan H. White-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry (RSC)-
dc.source.urihttp://dx.doi.org/10.1039/a800871j-
dc.titlePreparation and reactions of some neutral pentamethylcyclopentadienylruthenium vinylidene complexes-
dc.typeJournal article-
dc.identifier.doi10.1039/a800871j-
pubs.publication-statusPublished-
dc.identifier.orcidBruce, M. [0000-0002-8377-7186]-
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