| Literature DB >> 34200677 |
Federico Bonaldo1, Fulvio Mattivi2, Daniele Catorci1, Panagiotis Arapitsas3, Graziano Guella1.
Abstract
Several classes of flavonoids, such as anthocyanins, flavonols, flavanols, and flavones, undergo a slow H/D exchange on aromatic ring A, leading to full deuteration at positions C(6) and C(8). Within the flavanol class, H-C(6) and H-C(8) of catechin and epicatechin are slowly exchanged in D2O to the corresponding deuterated analogues. Even quercetin, a relevant flavonol representative, shows the same behaviour in a D2O/DMSOd6 1:1 solution. Detailed kinetic measurements of these H/D exchange processes are here reported by exploiting the time-dependent changes of their peak areas in the 1H-NMR spectra taken at different temperatures. A unifying reaction mechanism is also proposed based on our detailed kinetic observations, even taking into account pH and solvent effects. Molecular modelling and QM calculations were also carried out to shed more light on several molecular details of the proposed mechanism.Entities:
Keywords: H/D isotopic exchange; NMR spectroscopy; flavonoids; kinetics; reaction mechanism
Year: 2021 PMID: 34200677 DOI: 10.3390/molecules26123544
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411