Radical scavenging reactions of chlorogenic acid: A pulse radiolysis study

Radical scavenging reactions of chlorogenic acid: A pulse radiolysis study At near neutral pH (approx. 5.5), the OH-adduct of chlorogenic acid (CGA), formed on pulse radiolysis of N2O-saturated aqueous CGA solutions (λ max = 400 and 450 nm) with k = 9 × 109 dm3 mol−1 s−1, rapidly eliminates water (k = 1 × 103 s−1) to give a resonance-stabilized phenoxyl type of radical. Oxygen rapidly adds to the OH-adduct of CGA (pH 5.5) to form a peroxyl type of radical (k = 6 × 107 dm3 mol−1 s−1). At pH 10.5, where both the hydroxyl groups of CGA are deprotonated, the rate of reaction of · OH radicals with CGA was essentially the same as at pH 5.5, although there was a marked shift in the absorption maximum to approx. 500 nm. The CGA phenoxyl radical formed with more specific one-electron oxidants, viz., Br 2 ·− and N 3 · radicals show an absorption maximum at 385 and 500 nm, k ranging from 1–5.5 × 109 dm3 mol−1 s−1. Reactions of other one-electron oxidants, viz., NO 2 · , NO· and CCl3OO· radicals, are also discussed. Repair rates of thymidine, cytidine and guanosine radicals generated pulse radiolytically at pH 9.5 by CGA are in the range of (0.7–3) × 109 dm3 mol−1 s−1. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Research on Chemical Intermediates Springer Journals

Radical scavenging reactions of chlorogenic acid: A pulse radiolysis study

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Publisher
Springer Journals
Copyright
Copyright © 2006 by VSP
Subject
Chemistry; Inorganic Chemistry; Physical Chemistry; Catalysis
ISSN
0922-6168
eISSN
1568-5675
D.O.I.
10.1163/156856706778400343
Publisher site
See Article on Publisher Site

Abstract

At near neutral pH (approx. 5.5), the OH-adduct of chlorogenic acid (CGA), formed on pulse radiolysis of N2O-saturated aqueous CGA solutions (λ max = 400 and 450 nm) with k = 9 × 109 dm3 mol−1 s−1, rapidly eliminates water (k = 1 × 103 s−1) to give a resonance-stabilized phenoxyl type of radical. Oxygen rapidly adds to the OH-adduct of CGA (pH 5.5) to form a peroxyl type of radical (k = 6 × 107 dm3 mol−1 s−1). At pH 10.5, where both the hydroxyl groups of CGA are deprotonated, the rate of reaction of · OH radicals with CGA was essentially the same as at pH 5.5, although there was a marked shift in the absorption maximum to approx. 500 nm. The CGA phenoxyl radical formed with more specific one-electron oxidants, viz., Br 2 ·− and N 3 · radicals show an absorption maximum at 385 and 500 nm, k ranging from 1–5.5 × 109 dm3 mol−1 s−1. Reactions of other one-electron oxidants, viz., NO 2 · , NO· and CCl3OO· radicals, are also discussed. Repair rates of thymidine, cytidine and guanosine radicals generated pulse radiolytically at pH 9.5 by CGA are in the range of (0.7–3) × 109 dm3 mol−1 s−1.

Journal

Research on Chemical IntermediatesSpringer Journals

Published: Jan 1, 2006

References

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