Premium
Determination of dissociation constants of flavonoids by capillary electrophoresis
Author(s) -
HerreroMartínez José M.,
Sanmartin Meritxell,
Rosés Martí,
Bosch Elisabeth,
Ràfols Clara
Publication year - 2005
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/elps.200410258
Subject(s) - flavonols , deprotonation , morin , chemistry , capillary electrophoresis , dissociation constant , catechin , quercetin , fisetin , dissociation (chemistry) , ring (chemistry) , chromatography , analytical chemistry (journal) , computational chemistry , polyphenol , organic chemistry , biochemistry , ion , medicine , receptor , pathology , antioxidant
Ionization constants of some flavanols (catechin and epicatechin) and flavonols (kaempherol, fisetin, morin, and quercetin) are determined by capillary zone electrophoresis (CZE). This technique allows the determination of p K a values until about 12. The p K a values obtained are compared with those calculated by the SPARC computational program. This program predicts the microscopic and macroscopic p K a values and the order of deprotonation of the different −OH groups. While for catechin and epicatechin the first ionizable OH group occurs in ring 1 and the second ionizable group in ring 2, in flavonols the first deprotonation occurs in ring 2 and the second in ring 1.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom