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Tautomerism and dual fluorescence in 9-substituted n-propyl- and methoxyethyl-porphycenes

Producción científica: Artículo en revista indizadaArtículorevisión exhaustiva

13 Citas (Web of Science)

Resumen

Dual fluorescence is described and characterized for several 9-substituted porphycenes. Using both spectroscopic and computational studies, the phenomenon is related to the differential stabilization of the two trans tautomers in the excited state. The electronic nature of the 9-substituents affects both the energy and the lifetime of the two tautomers as well as their interconversion. The results are consistent with a two-step model for excited-state tautomerization that involves the population of an upper excited state, tentatively assigned to a cis species, which in turn provides an efficient non-radiative pathway to the ground state.

Idioma originalInglés
Páginas (desde-hasta)633-640
Número de páginas8
PublicaciónJournal of Porphyrins and Phthalocyanines
Volumen16
N.º5-6
DOI
EstadoPublicada - 2012

Huella

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