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dc.contributor.authorLorusso, Patrizia
dc.contributor.authorEastham, Graham
dc.contributor.authorCole-Hamilton, David J.
dc.date.accessioned2019-06-14T23:40:39Z
dc.date.available2019-06-14T23:40:39Z
dc.date.issued2018-06-15
dc.identifier253403071
dc.identifier1e562491-8047-4762-a05c-e0f9df6fe023
dc.identifier85050187453
dc.identifier000444187700024
dc.identifier.citationLorusso , P , Eastham , G & Cole-Hamilton , D J 2018 , ' Insight into the mechanism of decarbonylation of methanol by ruthenium complexes; a deuterium labelling study ' , Dalton Transactions , vol. In press . https://doi.org/10.1039/C8DT01733Fen
dc.identifier.issn1477-9226
dc.identifier.urihttps://hdl.handle.net/10023/17902
dc.descriptionThe authors thank Lucite international for funding.en
dc.description.abstractIn the reaction of [RuHClP3] (P = PPh3) with NaOMe in methanol, the product is [RuH2(CO)P3]. Short reaction times show that the final product is formed through [RuH4P3] as the major intermediate. Using NaOCD3 in CD3OD, the first formed product is [RuH4P'3] (P' is PPh3 partially deuterated in the ortho positions of the aromatic rings). Further reaction leads to a mixture of [RuHnD2-n(CO)P3] (n = 0, 22 %; n = 1, 2 isomers each 28 %; n = 2, 22 %). Mechanistic aspects of both steps of the reaction are explored and, together with previously published calculations, they provide definitive mechanisms for both dehydrogenation and decarbonylation in these interesting systems.
dc.format.extent1275003
dc.language.isoeng
dc.relation.ispartofDalton Transactionsen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subject.lccQDen
dc.titleInsight into the mechanism of decarbonylation of methanol by ruthenium complexes; a deuterium labelling studyen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doi10.1039/C8DT01733F
dc.description.statusPeer revieweden
dc.date.embargoedUntil2019-06-15
dc.identifier.urlhttp://www.rsc.org/suppdata/c8/dt/c8dt01733f/c8dt01733f1.pdfen


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