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...
| Autores: | , |
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| 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 |
| 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. |
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