7-Hydroxyflavone Revisited: Spectral, Acid–Base Properties, and Interplay of the Protolytic Forms in the Ground and Excited States
Author:
Affiliation:
1. Institute of Chemistry, Kharkiv V.N. Karazin National University, Svoboda 4, 61077 Kharkiv, Ukraine
2. Faculty of Chemistry, University of Gdańsk, Wita Stwosza 63, 80-952 Gdańsk, Poland
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp412334x
Reference42 articles.
1. Valant-Vetschera, K. M.; Wollenweber, E.InFlavonoids: Chemistry, Biochemistry, and Applications;Andersen, Ø.M., Markham, K. R., Eds.Taylor & Francis Group:Boca Raton, FL, 2006; pp617–748.
2. Ultraviolet absorption of flavonoids II. Ionization constants of 7- and 4?-hydroxy derivatives of flavone and flavonol
3. Ultraviolet absorption of flavonoids VIII. Ionization constants of kaempferol and quercetin
4. Absorption and Fluorescence Spectra, pKa Values, and Fluorescence Lifetimes of Monohydroxyflavones and Monomethoxyflavones
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