One-electron redox reactions of troxerutin in aqueous solutions

One-electron redox reactions of troxerutin in aqueous solutions The oxidation of flavonoids is of great interest because of their action as antioxidants with the ability to scavenge radicals by means of electron-transfer processes. The redox reactions of the flavonoid derivative troxerutin, (2-[3,4-bis-(2-hydroxyethoxy) phenyl]-3[[6-deoxy-α-L-manno-pyranosyl)-β-(D-glucopyranosyl]-oxy]-5-hydroxy-7-(2-hydroxyethoxy)-4H-1-benzo-pyran-4-one), were investigated over a wide range of conditions, using pulse radiolysis and cyclic voltammetry. The oxidation mechanism proceeds in sequential steps. One-electron redox potentials for troxerutin were found to be +1.196, +0.846 and −0.634 V vs. NHE. Research on Chemical Intermediates Springer Journals

One-electron redox reactions of troxerutin in aqueous solutions

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Brill Academic Publishers
Copyright © 2005 by VSP
Chemistry; Inorganic Chemistry; Physical Chemistry; Catalysis
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