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dc.contributor.authorAlabau, Roberto G.es_ES
dc.contributor.authorEsteruelas, Miguel A.es_ES
dc.contributor.authorOliván, Montserrates_ES
dc.contributor.authorOñate, Enriquees_ES
dc.contributor.authorPalacios, Adriánes_ES
dc.contributor.authorTsai, Jui-Yies_ES
dc.contributor.authorXia, Chuanjunes_ES
dc.date.accessioned2016-12-12T10:45:45Z-
dc.date.available2016-12-12T10:45:45Z-
dc.date.issued2016-11-
dc.identifier.citationOrganometallics 35(23): 3981-3995 (2016)es_ES
dc.identifier.issn0276-7333-
dc.identifier.urihttp://hdl.handle.net/10261/141299-
dc.description.abstractThe preparation of osmium(II) complexes containing a CC6H4,CBzIm,CBzIm,CC6H4-tetradentate ligand with a −CH2CH2– link between the benzimidazolidene (BzIm) groups is described, and the influence of the link on their structures and emissive properties is analyzed. The hexahydride complex OsH6(PiPr3)2 (1) reacts with 1,1′-diphenyl-3,3′-ethylenedibenzimidazolium bromide in dimethylformamide to afford OsBr{κ3-C,C,C-(C6H4-BzIm-CH2CH2-BzIm-Ph)}(CO)(PiPr3)2 (2), as a result of the direct metalation of both benzimidazolium moieties of the salt, the o-CH bond activation of a phenyl substituent, and the carbonylation of the metal center by action of the solvent. Treatment of 2 with Na[BH4] leads to the hydride derivative OsH{κ3-C,C,C-(C6H4-BzIm-CH2CH2-BzIm-Ph)}(CO)(PiPr3)2 (3), which evolves into Os{κ4-C,C,C,C-(C6H4-BzIm-CH2CH2-BzIm-C6H4)}(CO)(PiPr3)2 (4) as a consequence of the assisted C–H bond activation of the second phenyl substituent. The use of dimethyl sulfoxide instead of dimethylformamide allows the generation of the tetradentate ligand in one pot. Stirring of dimethyl sulfoxide solutions of 1 leads to Os{κ4-C,C,C,C-(C6H4-BzIm-CH2CH2-BzIm-C6H4)}(DMSO)2 (5). The solvent molecules of 5 can be displaced by 1,2-bis(diphenylphosphino)ethylene (bdppe), 1,2-bis(diphenylphosphino)benzene (dppbz), and tetrafluorobenzobarrelene (TFB) to yield the [4 + 2] derivatives Os{κ4-C,C,C,C-(C6H4-BzIm-CH2CH2-BzIm-C6H4)}L2 (L2 = bdppe (6), dppbz (7), TFB (8)). The X-ray structures of 4, 6, and 7 reveal that, in these compounds, the tetradentate ligand adopts a mer three-planar disposition of a phenyl and two benzimidazolidene groups with the other phenyl group situated in a perpendicular direction disposed trans to L. The reason for this preference is electronic. Thus, the stereochemistry of 7 is the same as that found in the related complexes Os{κ2-C,C-(MeBzIm-C6H4)}2(dppbz) (13) and Os{κ2-C,C-(MeBzIm*-C6H4)}2(dppbz) (14) containing two free ortho-metalated N-phenylbenzimidazolidene ligands. Complexes 7, 13, and 14 are phosphorescent. The first of them shows emissions narrower and bluer than those of 13 and 14.es_ES
dc.description.sponsorshipFinancial support from the MINECO of Spain (Projects CTQ2014-52799-P and CTQ2014-51912-REDC), the Diputación General de Aragón (E-35), FEDER, and the European Social Fund is acknowledged.es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.relationMINECO/ICTI2013-2016/CTQ2014-51912-REDCes_ES
dc.relationMINECO/ICTI2013-2016/CTQ2014-52799-Pes_ES
dc.relation.isversionofPostprintes_ES
dc.rightsopenAccessen_EN
dc.titleOsmium(II) complexes containing a dianionic CCCC-donor tetradentate ligandes_ES
dc.typeartículoes_ES
dc.identifier.doihttp://dx.doi.org/10.1021/acs.organomet.6b00776-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1021/acs.organomet.6b00776es_ES
dc.identifier.e-issn1520-6041-
dc.embargo.terms2017-11-30es_ES
dc.contributor.funderDiputación General de Aragónes_ES
dc.contributor.funderMinisterio de Economía y Competitividad (España)es_ES
dc.contributor.funderEuropean Commissiones_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
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