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dc.contributor.authorBaya, Miguel-
dc.contributor.authorBuil, María L.-
dc.contributor.authorEsteruelas, Miguel A.-
dc.contributor.authorOñate, Enrique-
dc.date.accessioned2013-01-28T13:07:29Z-
dc.date.available2013-01-28T13:07:29Z-
dc.date.issued2005-
dc.identifierdoi: 10.1021/om050487q-
dc.identifierissn: 0276-7333-
dc.identifiere-issn: 1520-6041-
dc.identifier.citationOrganometallics 24(21): 5180-5183 (2005)-
dc.identifier.urihttp://hdl.handle.net/10261/65283-
dc.description.abstractComplex Os(η5-C5H5)(C≡CPh) {[η2-CH2=C-(CH3)]PiPr 2} (1) reacts with HBF4·OEt2 to give the π-alkyne derivative [Os(η5-C5H5) (η2-HC≡CPh){η2-CH2=C(CH 3)]PiPr2}]BF4 (2), which is transformed to [Os(η5-C5H5)(1,2-dihydro-2- methylnaphth-2-yldiisopropylphosphine)]BF4 (3) as a result of the coupling of the alkyne with the isopropenyl substituent of the starting phosphine. The tridentate coordination mode of the dihydronaphthylphosphine in 3 is proved by X-ray diffraction analysis. © 2005 American Chemical Society.-
dc.description.sponsorshipFinancial support from the MCYT of Spain (Project BQU2002-00606, PPQ2000-0488-P4-02) is acknowledged. M.L.B. thanks the Spanish MCYT/Universidad de Zaragoza for funding through the “Ramón y Cajal” program. -
dc.language.isoeng-
dc.publisherAmerican Chemical Society-
dc.rightsclosedAccess-
dc.titleThe cyclopentadienyl-osmium moiety as template for the formation of a dihydronaphthylphosphine by coupling between phenylacetylene and an α-alkenylphosphine-
dc.typeartículo-
dc.identifier.doi10.1021/om050487q-
dc.date.updated2013-01-28T13:07:29Z-
dc.description.versionPeer Reviewed-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
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