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Flavonols and Crown-Flavonols as Metal Cation Chelators. The Different Nature of Ba2+and Mg2+Complexes
Author(s) -
Alexander D. Roshal,
A. V. Grigorovich,
А. О. Дорошенко,
Vasyl G. Pivovarenko,
Alexander P. Demchenko
Publication year - 1998
Publication title -
the journal of physical chemistry a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 235
eISSN - 1520-5215
pISSN - 1089-5639
DOI - 10.1021/jp972519w
Subject(s) - flavonols , chemistry , crown (dentistry) , metal , nuclear chemistry , organic chemistry , quercetin , materials science , antioxidant , composite material
The derivatives of 3-hydroxyflavone exhibit excited-state intramolecular proton transfer (ESIPT) reaction with significant (60−80 nm) shifts of fluorescence spectra between normal and phototautomer forms. This fact makes these compounds attractive as fluorescence probes in analytical chemistry, biophysics, and molecular biology. Different flavonol derivatives, including 4‘-(monoaza-15-crown-5)flavonol, were synthesized, and their absorption and fluorescent spectra were studied in acetonitrile in the presence of different concentrations of Mg2+ and Ba2+ ions. It was shown that the general feature of flavonols is the ability to form two types of complexes with alkaline-earth cations:  the low-stability “external” and high-stability chelating complexes. On the formation of the complexes, parent flavonols and their 4‘-dialkylamino derivatives undergo different perturbations of their electronic structures. 4‘-(Monoaza-15-crown-5)flavonol forms two types of complexes with both Mg2+ and Ba2+ ions; the sequence o...

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