Spectroscopy and photophysics of 4- and 7-hydroxycoumarins and their thione analogs

Acid-base equilibria were studied for 4-hydroxycoumarin, 7-hydroxy-4-methylcoumarin and their thione derivatives in different media for their ground and lowest energy singlet and triplet excited states. The ethoxylated and/or methoxylated derivatives were also investigated. Characterization involves...

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Detalhes bibliográficos
Autor principal: Seixas de Melo, J. (author)
Outros Autores: Fernandes, P. F. (author)
Formato: article
Idioma:eng
Publicado em: 2001
Assuntos:
Texto completo:http://hdl.handle.net/10316/5212
País:Portugal
Oai:oai:estudogeral.sib.uc.pt:10316/5212
Descrição
Resumo:Acid-base equilibria were studied for 4-hydroxycoumarin, 7-hydroxy-4-methylcoumarin and their thione derivatives in different media for their ground and lowest energy singlet and triplet excited states. The ethoxylated and/or methoxylated derivatives were also investigated. Characterization involves fluorescence spectra, quantum yields, lifetimes, phosphorescence spectra, lifetimes, and triplet-triplet absorption spectra. From their pKa values it was found that 4 and 7-hydroxycoumarins are more acidic in their lowest excited singlet states than in S0. The origin and character of the lowest singlet and triplet excited states is discussed.