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dc.contributor.authorCrespo, Olga-
dc.contributor.authorDíez-Gil, César-
dc.contributor.authorGimeno, M. Concepción-
dc.contributor.authorLaguna, Antonio-
dc.contributor.authorMonge, Miguel-
dc.contributor.authorOspino, Isaura-
dc.date.accessioned2013-01-22T13:48:24Z-
dc.date.available2013-01-22T13:48:24Z-
dc.date.issued2011-
dc.identifierdoi: 10.1039/c1dt10890e-
dc.identifierissn: 1477-9226-
dc.identifiere-issn: 1477-9234-
dc.identifier.citationDalton Transactions 40(39): 10038-10046 (2011)-
dc.identifier.urihttp://hdl.handle.net/10261/64721-
dc.description.abstractReaction of the yellow-green emitters [Au{(PPh2) 2C2B9H10}(PR3)] with [Au(C6F5)(tht)] affords orange-red emissive gold complexes [Au2{ο-(PPh2)2C2B 9H10}(C6F5)(PR3)] which contain different neutral (PR3) and anionic (C6F 5) auxiliary ligands and an anionic diphosphine. The resulting complexes are among the few reported in which an ortho-carborane diphosphine acts in a bridging mode, and are unique in containing not a closo- (neutral), but a nido-carborane (anionic) cluster. DFT and TDDFT calculations led to the prediction of the origin of the two first singlet-triplet transitions, which is consistent with the experimental results. Although the blue emissive nido-diphosphine plays a key role in the transitions of the three-coordinate precursors and the final dinuclear complexes, it is the environment around the gold centre that controls the emission energy. © The Royal Society of Chemistry 2011.-
dc.description.sponsorshipWe thank the Ministerio de Ciencia e Innovación D.G.I. (CTQ2010-20500-C02-01).-
dc.language.isoeng-
dc.publisherRoyal Society of Chemistry (UK)-
dc.rightsclosedAccess-
dc.titleHighly emissive dinuclear complexes [Au2{μ-(PPh2)2C2B9H10}(C6F5)(PR3)] with different gold fragments coordinated to an anionic diphosphine-
dc.typeartículo-
dc.identifier.doi10.1039/c1dt10890e-
dc.date.updated2013-01-22T13:48:24Z-
dc.description.versionPeer Reviewed-
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