Issue 8, 2017

Photophysics of 7-mercapto-4-methylcoumarin and derivatives: complementary fluorescence behaviour to 7-hydroxycoumarins

Abstract

The photophysical behaviour of 7-mercapto-4-methylcoumarin (C-SH) and derivatives has been studied in different solvents. In contrast to 7-hydroxy-4-methylcoumarin, C-SH shows poor emission, but high fluorescence when the thiol is alkylated. The origin and character of the lowest singlet states are discussed, specifically proposing that the thione-like C[double bond, length as m-dash]S resonance form plays a key role in excited state deactivation in C-SH.

Graphical abstract: Photophysics of 7-mercapto-4-methylcoumarin and derivatives: complementary fluorescence behaviour to 7-hydroxycoumarins

Supplementary files

Article information

Article type
Paper
Submitted
01 Apr 2017
Accepted
15 Jun 2017
First published
15 Jun 2017

Photochem. Photobiol. Sci., 2017,16, 1284-1289

Photophysics of 7-mercapto-4-methylcoumarin and derivatives: complementary fluorescence behaviour to 7-hydroxycoumarins

A. E. Lanterna, M. González-Béjar, M. Frenette and J. C. Scaiano, Photochem. Photobiol. Sci., 2017, 16, 1284 DOI: 10.1039/C7PP00121E

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