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Authordc.contributor.authorDiaz, Eloisa 
Admission datedc.date.accessioned2018-12-20T15:04:44Z
Available datedc.date.available2018-12-20T15:04:44Z
Publication datedc.date.issued1999
Cita de ítemdc.identifier.citationBoletin de la Sociedad Chilena de Quimica, Volumen 44, Issue 3, 2018, Pages 315-320
Identifierdc.identifier.issn03661644
Identifierdc.identifier.other10.4067/S0366-16441999000300008
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/157615
Abstractdc.description.abstractThe EPR spectra of a series of mononuclear complexes [CpFe(dppe)SR]PF6 R = C6H5 (1), C3H7 (2), p-C6H4Br (3) and the binuclear [CpFe(dppe)-S-CH2CH2-S-CpFe(dppe)](PF6) 2 (4) were measured. All the paramagnetic complexes exhibit intense signals in both solid state as well as in CH2Cl2 solution. Analysis of the spectra indicates a pseudooctahedral structure for the complexes except for complex (2) for which a tetragonal distortion in solid state was observed. Some degree of delocalization of the unpaired electron for (3) and (4) was suggested. The stabilization of the radicals by the thiolate ligands is discussed.
Lenguagedc.language.isoen
Publisherdc.publisherSociedad Chilena de Quimica
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceBoletin de la Sociedad Chilena de Quimica
Keywordsdc.subjectEPR
Keywordsdc.subjectIron-sulfur complexes
Keywordsdc.subjectOrganometallic radical
Keywordsdc.subjectThiolate compounds
Títulodc.titleObservation of stable 17 e iron(III) cyclopentadienyl radical complexes
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile