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The Antioxidant Activity of Quercetin in Water Solution

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Date 2019 May 21
PMID 31105172
Citations 22
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Abstract

Despite its importance, little is known about the absolute performance and the mechanism for quercetin's antioxidant activity in water solution. We have investigated this aspect by combining differential oxygen-uptake kinetic measurements and B3LYP/6311+g (d,p) calculations. At pH = 2.1 (30 °C), quercetin had modest activity ( = 4.0 × 10 M s), superimposable to catechol. On raising the pH to 7.4, reactivity was boosted 40-fold, trapping two peroxyl radicals in the chromen-4-one core and two in the catechol with of 1.6 × 10 and 7.0 × 10 M s. Reaction occurs from the equilibrating mono-anions in positions 4' and 7 and involves firstly the OH in position 3, having bond dissociation enthalpies of 75.0 and 78.7 kcal/mol, respectively, for the two anions. Reaction proceeds by a combination of proton-coupled electron-transfer mechanisms: electron⁻proton transfer (EPT) and sequential proton loss electron transfer (SPLET). Our results help rationalize quercetin's reactivity with peroxyl radicals and its importance under biomimetic settings, to act as a nutritional antioxidant.

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References
1.
Valgimigli L, Amorati R, Petrucci S, Pedulli G, Hu D, Hanthorn J . Unexpected acid catalysis in reactions of peroxyl radicals with phenols. Angew Chem Int Ed Engl. 2009; 48(44):8348-51. DOI: 10.1002/anie.200903360. View

2.
Guerra M, Amorati R, Pedulli G . Water effect on the o-h dissociation enthalpy of para-substituted phenols: a DFT study. J Org Chem. 2004; 69(16):5460-7. DOI: 10.1021/jo0495236. View

3.
Wu M, Cao Z, Zhao Y, Zeng R, Tu M, Zhao J . Novel self-assembled pH-responsive biomimetic nanocarriers for drug delivery. Mater Sci Eng C Mater Biol Appl. 2016; 64:346-353. DOI: 10.1016/j.msec.2016.03.099. View

4.
Lalevee J, Allonas X, Fouassier J, Ingold K . Absolute rate constants for some intermolecular reactions of alpha-aminoalkylperoxyl radicals. Comparison with alkylperoxyls. J Org Chem. 2008; 73(17):6489-96. DOI: 10.1021/jo800925g. View

5.
Matera R, Gabbanini S, Berretti S, Amorati R, De Nicola G, Iori R . Acylated anthocyanins from sprouts of Raphanus sativus cv. Sango: isolation, structure elucidation and antioxidant activity. Food Chem. 2014; 166:397-406. DOI: 10.1016/j.foodchem.2014.06.056. View