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Inactivation of Pathogens via Visible-Light Photolysis of Riboflavin-5′-Phosphate
Published on: April 6, 2022
Deactivation of the first excited singlet state of thiophenols
Yasser M Riyad1, Sergej Naumov, Ralf Hermann
1University of Leipzig, Interdisciplinary Group Time-Resolved Spectroscopy, Permoserstr. 15, D-4303, Leipzig, Germany.
Abstract:
On the bases of picosecond and nanosecond laser flash photolysis with detection by emission and absorption spectroscopy, a quantitative description is given of all deactivation channels of the first excited singlet state of thiophenols ArSH(S(1)) such as fluorescence, intersystem crossing (ISC), chemical dissociation into radicals, and radiation-less internal conversion (IC). For this purpose, the photolysis of thiophenol and its methyl-, methoxy-, and chloro-substituted derivatives was studied in solvents of increasing polarity: 1-chlorobutane, ethanol, and acetonitrile. The fluorescence lifetime of the thiophenols was found to range from some hundreds of picoseconds up to a few nanoseconds, correlating with fluorescence quantum yields between 0.001-0.040, at room temperature. Depending on the substitution pattern of the aromatic ring, the quantum yield of the S-H bond dissociation was found to be between 0.3-0.5, irrespective of the solvent polarity. In laser photolysis, no triplet formation of the investigated compounds could be observed neither by the direct way nor by subsequent sensitization with beta-carotene. As a difference to the total, the radiation-less internal conversion (Phi(IC)>or= 0.5) was found to be the dominating process.
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