Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/17791
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dc.contributor.authorBruce, M.-
dc.contributor.authorEllis, B.-
dc.contributor.authorSkelton, B.-
dc.contributor.authorWhite, A.-
dc.date.issued2005-
dc.identifier.citationJournal of Organometallic Chemistry, 2005; 690(7):1772-1783-
dc.identifier.issn0022-328X-
dc.identifier.urihttp://hdl.handle.net/2440/17791-
dc.descriptionCopyright © 2005 Elsevier B.V. All rights reserved.-
dc.description.abstractSeveral complexes have been obtained from reactions carried out in early attempts to prepare the diynyl complexes Ru(C≡CC≡CR)(dppe)Cp* (R = H, SiMe3). These have been identified crystallographically as the acyl complex Ru{C≡CC(O)Me}(dppe)Cp* (3), the cationic imido complex [Ru{C≡CC(=NH2)Me}(dppe)Cp*]PF6 (4), the binuclear butenynylallenylidene [{Ru(dppe)Cp*}2{μ- C≡CC(OMe)=CHCMe=C=C=}]PF6 (5), and the bis(ethynyl) cyclobutenylidene [{Ru(dppe)Cp*}2{μ-C≡CC 4H2(SiMe3)C≡C}]PF6 (6). NMR studies of 5 have revealed the existence of two isomers. Plausible routes for their formation from the putative butatrienylidene intermediate [Ru(=C=C=C=CH2)(dppe)Cp*]+ (A) are discussed. © 2005 Elsevier B.V. All rights reserved.-
dc.description.statementofresponsibilityMichael I. Bruce, Benjamin G. Ellis, Brian W. Skelton and Allan H. White-
dc.description.urihttp://www.elsevier.com/wps/find/journaldescription.cws_home/504090/description#description-
dc.language.isoen-
dc.publisherElsevier Science Sa-
dc.source.urihttp://dx.doi.org/10.1016/j.jorganchem.2005.01.035-
dc.titleFurther chemistry of ruthenium butatrienylidene complexes-
dc.typeJournal article-
dc.identifier.doi10.1016/j.jorganchem.2005.01.035-
pubs.publication-statusPublished-
dc.identifier.orcidBruce, M. [0000-0002-8377-7186]-
Appears in Collections:Aurora harvest 2
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