INQUIMAE   12526
INSTITUTO DE QUIMICA, FISICA DE LOS MATERIALES, MEDIOAMBIENTE Y ENERGIA
Unidad Ejecutora - UE
artículos
Título:
Photosubstitution of Monodentate Ligands from Ru(II)-dicarboxybipyridine complexes
Autor/es:
BARALDO, LUIS M.; CARABALLO, ROLANDO M.; ROSI, PABLO; HODAK, JOSÉ H.
Revista:
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Editorial:
WILEY-V C H VERLAG GMBH
Referencias:
Lugar: Weinheim; Año: 2017 p. 3612 - 3612
ISSN:
1434-1948
Resumen:
In this work, we report the photophysical and photochemical properties of Ru(II) polypyridine complexes [Ru(bpy)(dcbpy)py2)]2+ (1)2+ and [Ru(dcbpy)2py2)]2+ (2)2+ (bpy= 2,2´-bipyridine, dcbpy= 4,4´-dicarboxy-2,2´-bipyridine, py= pyridine). These complexes combine a monodentate ligand with a chelate bipyridine substituted with carboxylate groups. At low pH both complexes present metal-to-ligand charge transfer (MLCT) absorption bands in the visible region and room temperature photoluminescence (PL) with long excited state lifetimes (τ > 200 ns). At physiological pH their absorption and emission maxima are displaced to higher energies with a significant reduction of their emission lifetime. These species show photosubstitution of the monodentate pyridine upon irradiation at 450 nm. At low pH the quantum yield for this process is very low, but at physiological pH they are very active, with a φPS,450 of 0.14 for (1)2+ and 0.17 for (2)2+. The products of photosubstitution were identified as the monoaquo complexes. Both, the reactants and the products of the photosubstitution show photoluminescence, but with very different lifetimes making it possible to follow the reaction by the time constant of their decay. The ability of complexes (1)2+ and (2)2+ to photorelease monodentate ligands at physiological pH makes them attractive candidates for the delivery of biomolecules linked to more complex structures through the carboxylate functional group.