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dc.creatorTerencio, T.es
dc.creatorBastardis, R.es
dc.creatorSuaud, N.es
dc.creatorMaynau, Danieles
dc.creatorBonvoisin, J.es
dc.creatorMalrieu, J. P.es
dc.creatorJiménez Calzado, Carmenes
dc.creatorGuihéry, Nathaliees
dc.date.accessioned2023-07-04T15:10:04Z
dc.date.available2023-07-04T15:10:04Z
dc.date.issued2011
dc.identifier.citationTerencio, T., Bastardis, R., Suaud, N., Maynau, D., Bonvoisin, J., Malrieu, J.P.,...,Guihéry, N. (2011). Physical analysis of the through-ligand long-distance magnetic coupling: Spin-polarization versus Anderson mechanism. Physical Chemistry Chemical Physics, 13 (26), 12314-12320. https://doi.org/10.1039/c1cp20179d.
dc.identifier.issn1463-9076es
dc.identifier.issn1463-9084es
dc.identifier.urihttps://hdl.handle.net/11441/147699
dc.description.abstractThe physical factors governing the magnetic coupling between two magnetic sites are analyzed and quantified as functions of the length of the bridging conjugated ligand. Using wave-function-theory based ab initio calculations, it has been possible to separate and calculate the various contributions to the magnetic coupling, i.e. the direct exchange, the spin polarization and the kinetic exchange. It is shown in model systems that while the Anderson mechanism brings the leading contribution for short-length ligands, the spin polarization dominates the through-long-ligand couplings. Since the spin polarization decreases more slowly than the kinetic exchange, highly spin polarizable bridging ligands would generate a good magneto-communication between interacting magnetic units.es
dc.formatapplication/pdfes
dc.format.extent19 p.es
dc.language.isoenges
dc.publisherRoyal Society of Chemistryes
dc.relation.ispartofPhysical Chemistry Chemical Physics, 13 (26), 12314-12320.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titlePhysical analysis of the through-ligand long-distance magnetic coupling: Spin-polarization versus Anderson mechanismes
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/acceptedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Química Físicaes
dc.relation.publisherversionhttps://doi.org/10.1039/c1cp20179des
dc.identifier.doi10.1039/c1cp20179des
dc.journaltitlePhysical Chemistry Chemical Physicses
dc.publication.volumen13es
dc.publication.issue26es
dc.publication.initialPage12314es
dc.publication.endPage12320es

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