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dc.contributor.authorPicazo, O.-
dc.contributor.authorAlkorta, Ibon-
dc.contributor.authorElguero, José-
dc.contributor.authorSundberg, M. R.-
dc.contributor.authorValo, J.-
dc.contributor.authorZborowski, K. K.-
dc.date.accessioned2013-02-01T12:25:47Z-
dc.date.available2013-02-01T12:25:47Z-
dc.date.issued2009-
dc.identifierdoi: 10.1007/s11224-009-9463-7-
dc.identifierissn: 1040-0400-
dc.identifiere-issn: 1572-9001-
dc.identifier.citationStructural Chemistry 20: 557- 563 (2009)-
dc.identifier.urihttp://hdl.handle.net/10261/65652-
dc.description.abstractA computational study of square planar organometallic complexes formed by the ligand 2,2′-bipyridine and all its possible difluoro derivatives in analogous position of the aromatic rings (n,n′-difluoro-2,2′-bipyridine, where n = n′ = 3, 4, 5, and 6) and two M-X2 (M = Pd and Pt and X = F, Cl, Br, and I) fragments has been carried out amounting to a total of 80 complexes. Relationships have been found between the chiral distinction energy and the different chemical moieties present. Using the statistical Free-Wilson method, the relative energies between the diastereomeric complexes have been correlated with the position of the substituent, the counter anion, and the central metal cation. © Springer Science+Business Media, LLC 2009.-
dc.language.isoeng-
dc.publisherKluwer Academic Publishers-
dc.rightsclosedAccess-
dc.titleChiral distinction in square planar Pt and Pd complexes of 2,2′-bipyridine derivatives-
dc.typeartículo-
dc.identifier.doi10.1007/s11224-009-9463-7-
dc.relation.publisherversionhttp://dx.doi.org/10.1007/s11224-009-9463-7-
dc.date.updated2013-02-01T12:25:47Z-
dc.description.versionPeer Reviewed-
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