Analogs of anthocyanins with a 3’,4’-dihydroxy substitution: Synthesis and investigation of their acid-base hydration metal binding and hydrogen-donating properties in aqueous solution.

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Mora-Soumille, Nathalie | Al Bittar, Sheiraz | Rosa, Maxence | Dangles, Olivier

Edité par CCSD ; Elsevier -

International audience. Analogs of anthocyanins with a 3 0 ,4 0-dihydroxy substitution: Synthesis and investigation of their acidebase, hydration, metal binding and hydrogen-donating properties in aqueous solution a b s t r a c t Glycosides of hydroxylated flavylium ions are proposed as pertinent analogs of anthocyanins, a major class of polyphenolic plant pigments. Anthocyanins with a 3 0 ,4 0-dihydroxy substitution on the Bring (catechol nucleus) are especially important for their metal chelating and electron-donating (antioxidant) capacities. In this work, an efficient chemical synthesis of 3 0 ,4 0-dihydroxy-7-O-b-D-glucopyranosyloxy-flavylium chloride and its aglycone is reported. Then, the ability of the two pigments to undergo proton transfer (formation of colored quinonoid bases) and add water (formation of a colorless chalcone) is investigated: at equilibrium the colored quinonoid bases (kinetic products) are present in very minor concentrations (<10% of the total pigment concentration) compared to the colorless chalcone (ther-modynamic product). The glucopyranosyloxyflavylium ion appears significantly less acidic than the aglycone. The thermodynamics of the overall sequence of flavylium e chalcone conversion is not affected by the b-D-glucosyl moiety while the kinetics appears slower by a factor ca. 8. Although the glucopyr-anosyloxyflavylium ion and its aglycone display similar affinities for Al 3þ , the Al 3þ-glucoside complex is more stable than the Al 3þ-aglycone complex due to the higher sensitivity of the latter to water addition and conversion into the corresponding chalcone. Finally, the glucopyranosyloxyflavylium ion and its aglycone are compared for their ability to reduce the 1,1-diphenyl-2-picrylhydrazyl radical in a mildly acidic water/MeOH (1:1) mixture as a first evaluation of their antioxidant activity. Glycosidation at C 7-OH results in a lower rate constant of first electron transfer to DPPH and a lower stoichiometry (total number of 1,1-diphenyl-2-picrylhydrazyl radicals reduced per pigment molecule). Anthocyanins are difficult to extract from plants in substantial amount. However, the analogs investigated in this work are of easy access by chemical synthesis and express the physico-chemical properties typical of anthocyanins. They can thus be regarded as valuable models for investigating the coloring, metal-binding and antioxidant properties of these important natural pigments.

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