New dinuclear asymmetric complexes of ruthenium and rhenium

New dinuclear asymmetric complexes of ruthenium and rhenium, of formula [(bpy)(CO)3 ReI(4,4′bpy)RunII/III (NH3)5]3+/4+ have been prepared and characterized by spectroscopic and electrochemical techniques. In the mixed-valent species [ReI, RuIII], the back electron transfer reaction RunII → ReII, tha...

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Detalles Bibliográficos
Autores: Fagalde, Florencia, Katz, Néstor Eduardo
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2001
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/53262
Acceso en línea:http://hdl.handle.net/11336/53262
Access Level:acceso abierto
Palabra clave:Asymmetric Complexes
Electron Transfer
Mixed-Valence
https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
Descripción
Sumario:New dinuclear asymmetric complexes of ruthenium and rhenium, of formula [(bpy)(CO)3 ReI(4,4′bpy)RunII/III (NH3)5]3+/4+ have been prepared and characterized by spectroscopic and electrochemical techniques. In the mixed-valent species [ReI, RuIII], the back electron transfer reaction RunII → ReII, that occurs after light excitation, is predicted to be in the Marcus inverted region. This fact is consistent with the observed quenching of the luminiscence of the Re chromophore in [(bpy)(CO)3ReI(4,4′-bpy)RuIII (NH3)5]4+, when compared to the parent complex [(bpy)(CO)3ReI(4,4′-bpy)]+. A theoretical treatment due to Creutz, Newton and Sutin has been successfully applied to predict the electronic coupling element in the mixed-valent complex.