Photophysics of Ru(II) Dyads Derived from Pyrenyl-Substitued Imidazo[4,5-f][1,10]phenanthroline Ligands.
Abstrakt
The photophysics of a series of Ru(II) dyads based on the 2-(1-pyrenyl)-1H-imidazo[4,5-f][1,10]-phenanthroline ligand was investigated. The ability of these metal complexes to intercalate DNA and induce cell death upon photoactivation makes them attractive photosensitizers for a range of photobiological applications, including photodynamic therapy. In the present study, time-resolved transient absorption and emission spectroscopy were used to interrogate the photoinduced processes that follow metal-to-ligand charge transfer excitation of the complexes in solution. It was found that energy transfer to pyrene-localized intraligand triplet states, facilitated by torsional motion of the pyrene moiety relative to the imidazo[4,5-f][1,10]phenanthroline ligand, was an important relaxation pathway governing the photophysical dynamics in this class of compounds. Biphasic decay kinetics were assigned to spontaneous (pre-equilibrium) and delayed emission, arising from an equilibrium established between (3)MLCT and (3)IL states. TDDFT calculations supported these interpretations.
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Informacje szczegółowe
- Kategoria:
- Publikacja w czasopiśmie
- Typ:
- artykuł w czasopiśmie wyróżnionym w JCR
- Opublikowano w:
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JOURNAL OF PHYSICAL CHEMISTRY A
nr 119,
strony 3986 - 3994,
ISSN: 1089-5639 - Język:
- angielski
- Rok wydania:
- 2015
- Opis bibliograficzny:
- Reichardt C., Pinto M., Wachtler M., Stephenson M., Kupfer S., Sainuddin T., Guthmuller J., Mcfarland S., Dietzek B.: Photophysics of Ru(II) Dyads Derived from Pyrenyl-Substitued Imidazo[4,5-f][1,10]phenanthroline Ligands.// JOURNAL OF PHYSICAL CHEMISTRY A. -Vol. 119, (2015), s.3986-3994
- DOI:
- Cyfrowy identyfikator dokumentu elektronicznego (otwiera się w nowej karcie) 10.1021/acs.jpca.5b01737
- Weryfikacja:
- Politechnika Gdańska
wyświetlono 132 razy
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