Photophysical and redox properties of dinuclear Ru and Os polypyridyl complexes with incorporated photostable spiropyran bridge
Articolo
Data di Pubblicazione:
2009
Citazione:
Photophysical and redox properties of dinuclear Ru and Os polypyridyl complexes with incorporated photostable spiropyran bridge / R.T.F. Jukes, B. Bozic, P. Belser, L. De Cola, F. Hartl. - In: INORGANIC CHEMISTRY. - ISSN 0020-1669. - 48:4(2009), pp. 1711-1721. [10.1021/ic800963u]
Abstract:
Aimed at creating a true photoswitchable energy transfer system, four dinuclear complexes containing ruthenium(ll) and osmium(ll) metal centers bridged by spiropyran-type linkers were designed and investigated. The bridge in its closed spiropyran form was shown to be a good insulator for energy transfer between the Ru-bpy donor and the Os-bpy acceptor (bpy = 2,2′-bipyridine). On the basis of properties of previously reported photochromic nitrospiropyrans substituted with a single polypyridine metal center, conversion of the bridge to the open merocyanine form was envisaged to result in efficient electronic energy transfer by a sequential ("hopping") mechanism. In contrast to the expectations, however, the studied closed-form dinuclear complexes remained stable independently of their photochemical or electrochemical activation. This difference in reactivity is attributed to the replacement of the nitro group by a second polypyridine metal center. We assume that these changes have fundamentally altered the excited-state and redox properties of the complexes, making the ring-opening pathways unavailable.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
electronic-energy transfer; luminescence properties; metal-complexes; ruthenium(II) complexes; intercomponent energy; exited-state; potentials; absorption; RU(II)/OS(II); lifetimes
Elenco autori:
R.T.F. Jukes, B. Bozic, P. Belser, L. De Cola, F. Hartl
Link alla scheda completa: