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dc.contributor.authorGarcía-Monforte, M. Ángeles-
dc.contributor.authorAra, Irene-
dc.contributor.authorMartín, Antonio-
dc.contributor.authorMenjón, Babil-
dc.contributor.authorTomás, Milagros-
dc.contributor.authorAlonso, Pablo J.-
dc.contributor.authorArauzo, Ana B.-
dc.contributor.authorMartínez, Jesús I.-
dc.contributor.authorRillo, Conrado-
dc.date.accessioned2015-03-04T09:18:00Z-
dc.date.available2015-03-04T09:18:00Z-
dc.date.issued2014-
dc.identifierdoi: 10.1021/ic501719y-
dc.identifierissn: 0020-1669-
dc.identifiere-issn: 1520-510X-
dc.identifier.citationInorganic Chemistry 53(23): 12384-12395 (2014)-
dc.identifier.urihttp://hdl.handle.net/10261/111750-
dc.description.abstractHomoleptic organocobalt(III) compounds with formula [NBu4][CoIII(C6X5)4] [X = F (3), Cl (4)] were obtained in reasonable yields by chemical oxidation of the corresponding divalent species [NBu4]2[CoII(C6X5)4] [X = F (1), Cl (2)]. The [CoIII(C6X5)4]-/[CoII(C6X5)4]2- couples are electrochemically related by quasi-reversible, one-electron exchange processes at moderate potential: E1/2 = -0.29 (X = F) and -0.36 V (X = Cl) versus saturated calomel electrode. The [CoIII(C6X5)4]- anions in salts 3 and 4 show an unusual square-planar geometry as established by single-crystal X-ray diffraction methods. According to their stereochemistry, these CoIII derivatives (d6) are paramagnetic non-Kramers systems with a large zero-field splitting contribution and no observable electron paramagnetic resonance (EPR) spectrum. The thermal dependence of their magnetic susceptibilities can be explained in terms of a spin-Hamiltonian formalism with S = 1 ground state (intermediate spin) and substantial spin-orbit contribution. The magnetic properties of the square-planar d7 parent species [NBu4]2[CoII(C6X5)4] were also thoroughly studied both at microscopic (EPR) and macroscopic levels (alternating current and direct current magnetization measurements). They behave as S = 1/2 (low spin) systems with mainly (dz2 )1 electron configuration and a certain degree of s-orbital admixture that has been quantified. The electronic structures of all four open-shell [Co(C6X5)4]q- compounds (q = 1, 2) accounting for their respective magnetic properties are based on a common orbital energy-level diagram.-
dc.description.sponsorshipThis work was supported by the Spanish MICINN (DGPTC)/FEDER (Project No. CTQ2008-06669-C02-01/BQU), MINECO/FEDER (Project Nos. CTQ2012-35251, MAT2011-23861, and MAT2011-27233-C02-1) and the Gobierno de Aragoń (Grupo Consolidado E21: Quımíca Inorgánica y de los Compuestos Organometálicos).-
dc.publisherAmerican Chemical Society-
dc.rightsclosedAccess-
dc.titleHomoleptic organocobalt(III) compounds with intermediate spin-
dc.typeArtículo-
dc.identifier.doi10.1021/ic501719y-
dc.date.updated2015-03-04T09:18:00Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.contributor.funderMinisterio de Ciencia e Innovación (España)-
dc.contributor.funderMinisterio de Economía y Competitividad (España)-
dc.contributor.funderEuropean Commission-
dc.contributor.funderGobierno de Aragón-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004837es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
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