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dc.contributor.authorGimeno, M. Concepción-
dc.contributor.authorLaguna, Antonio-
dc.contributor.authorVisbal, Renso-
dc.date.accessioned2013-01-23T12:41:42Z-
dc.date.available2013-01-23T12:41:42Z-
dc.date.issued2012-
dc.identifierdoi: 10.1021/om300571m-
dc.identifierissn: 0276-7333-
dc.identifiere-issn: 1520-6041-
dc.identifier.citationOrganometallics 31(20): 7146-7157 (2012)-
dc.identifier.urihttp://hdl.handle.net/10261/64862-
dc.description.abstractThe reaction of N-methyl (Me) or N-benzyl (Bn) imidazole with 9-chloroacridine (9-ClAcr) gives the corresponding imidazolium salts, [(RimAcr)H]Cl (R = Me, Bn), which can further react with AgBF 4 or [Au(C 6F 5)(tht)], affording the new salts [(RimAcr)H]BF 4 or [(RimAcr)H][Au(C 6F 5)Cl]. Silver(I) carbene complexes of the form [AgCl(RimAcr)] or [Ag(RimAcr) 2]BF 4 are synthesized by reaction of the corresponding imidazolium salts with Ag 2O or Ag 2O and NaOH. Transmetalation reactions allow the synthesis of the gold and copper derivatives [MCl(RimAcr)] (M = Au, Cu) and [Au(RimAcr) 2]BF 4. Treatment of [(RimAcr)H][Au(C 6F 5)Cl] with NaH affords the synthesis of the carbene complexes [Au(C 6F 5)(RimAcr)]. The crystal structures of these complexes show interesting π·· ·π stacking interactions between the acridine and/or the pentafluorophenyl groups. The imidazolium salts and the gold and silver complexes are intense blue-green emitters. © 2012 American Chemical Society.-
dc.description.sponsorshipAuthors thank the Ministerio de Economía y Competitividad (MEC/FEDER CTQ2010-20500-C02-01) for financial support. -
dc.language.isoeng-
dc.publisherAmerican Chemical Society-
dc.rightsclosedAccess-
dc.titleN-heterocyclic carbene coinage metal complexes as intense blue-green emitters-
dc.typeartículo-
dc.identifier.doi10.1021/om300571m-
dc.date.updated2013-01-23T12:41:42Z-
dc.description.versionPeer Reviewed-
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