Photophysics of thionine in AOT and BHDC reverse micelles. Quenching of the triplet state by aliphatic amines studied by transient absorption spectroscopy

The photophysics of thionine (3,7-diamino-5-phenothiazinium) (Th+) was investigated in reverse micelles (RMs) of sodium bis(2-ethylhexyl)sulfosuccinate (AOT) and benzyldimethylhexadecylammonium chloride (BHDC) with special emphasis on the triplet state processes. In RMs both the absorption and emission spectra of the dye present a red shift with respect to pure water. The absorption maximum wavelength and Stokes shift show a tendency towards the values in water, although do not reach them even with the higher water content examined. The photophysical parameters are more affected by the water content in BHDC than in AOT. The triplet state of Th+ was investigated by the technique of laser flash photolysis. The T-T absorption spectrum presents a strong absorption band in the region between 770 and 800 nm, corresponding to the monoprotonated triplet form of the dye. This spectrum is red shifted with respect to water in the RMs. The triplet quenching by aliphatic amines was investigated. The triplet decay is well fitted by a bi-exponential function in the presence of the hydro-soluble triethanolamine (TEOA) in both RMs. This behavior is interpreted as the result of a very fast intramicellar quenching, followed by slow process that may be ascribed to an intermicellar exchange of amine molecules between RMs. The kinetic analysis showed that intermicellar exchange rate constant is two orders of magnitude more effective in BHDC than in AOT. Meanwhile, in the quenching by the hydrophobic tributylamine (TBA) the decay is mono-exponential. The amine is located preferentially in the bulk organic phase and the quenching mechanism involves the interaction of the amine with the monoprotonated triplet of dye reaching in the micellar interface. It is interesting to note that the apparent quenching rate constant by TBA is one order of magnitude lower than the exchange rate constant by TEOA.Fil: Porcal, Gabriela Valeria. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; ArgentinaFil: Arbeloa, Ernesto Maximiliano. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; ArgentinaFil: Bertolotti, Sonia Graciela. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; ArgentinaFil: Previtali, Carlos Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentin