Electron-, proton-, and photon-induced spectroscopic changes in chromophore-quencher tricarbonyl(2,2′-Bipyridine)rhenium(I) complexes with 4,4′-azobis(pyridine)

We report in this work the synthesis and characterization of new mono- and dinuclear complexes of formulas: [Re(bpy)(CO)3(4,4′-azpy)] (CF3SO3), 1 (bpy = 2,2′-bipyridine, 4,4′-azpy = 4,4′-azobis(pyridine)); [(bpy)(CO)3Re(4,4′-azpy) Ru(NH3)5](PF6)3.CH 3CN•6H2O, 2 and the heterodinuclear species [(bpy)...

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Detalhes bibliográficos
Autores: Pourrieux, Gaston, Fagalde, Florencia, Romero, María Isabel, Fontrodona, Xaxier, Parella, Teodor, Katz, Néstor Eduardo
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2010
País:Argentina
Recursos:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/52927
Acesso em linha:http://hdl.handle.net/11336/52927
Access Level:acceso abierto
Palavra-chave:Rhenium(I) Complexes
4,4'-Azobis(Pyridine)
Photo-Induced
Trans-Cis Photoisomerization
https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
Descrição
Resumo:We report in this work the synthesis and characterization of new mono- and dinuclear complexes of formulas: [Re(bpy)(CO)3(4,4′-azpy)] (CF3SO3), 1 (bpy = 2,2′-bipyridine, 4,4′-azpy = 4,4′-azobis(pyridine)); [(bpy)(CO)3Re(4,4′-azpy) Ru(NH3)5](PF6)3.CH 3CN•6H2O, 2 and the heterodinuclear species [(bpy)(CO)3Re(4,4′-azpy)Ru(NH3)5] 4+, 3 (obtained in situ by electrochemical oxidation of 2). The molecular structure of 1 has been determined by X-ray diffraction. We also report the effect of controlled potential electrolysis, protonation, and light excitation on the absorption and emission properties of these complexes. In particular, complex 1, which is almost non-emissive at room temperature, recovers luminescence either by reduction of coordinated 4,4′-azpy or by trans- to cis-photoisomerization. The detected emission of 1 at 77 K is due to decay from a Re→ bpy metal-to-ligand charge transfer excited state. Time dependent density functional theory calculations support the interpretation of the photophysical changes induced by external stimuli.