Literature DB >> 28764012

Antioxidative mechanisms in chlorogenic acid.

Jelena Tošović1, Svetlana Marković2, Jasmina M Dimitrić Marković3, Miloš Mojović3, Dejan Milenković4.   

Abstract

Although chlorogenic acid (5CQA) is an important ingredient of various foods and beverages, mechanisms of its antioxidative action have not been fully clarified. Besides electron spin resonance experiment, this study includes thermodynamic and mechanistic investigations of the hydrogen atom transfer (HAT), radical adduct formation (RAF), sequential proton loss electron transfer (SPLET), and single electron transfer - proton transfer (SET-PT) mechanisms of 5CQA in benzene, ethanol, and water solutions. The calculations were performed using the M06-2X/6-311++G(d,p) level of theory and CPCM solvation model. It was found that SET-PT is not a plausible antioxidative mechanism of 5CQA. RAF pathways are faster, but HAT yields thermodynamically more stable radical products, indicating that in acidic and neutral media 5CQA can take either HAT or RAF pathways. In basic environment (e.g. at physiological pH) SPLET is the likely antioxidative mechanism of 5CQA with extremely high rate.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  5-O-caffeoylquinic acid (PubChem CID: 1794427); DFT calculations; ESR experiment; Kinetic approach; Thermodynamic approach

Mesh:

Substances:

Year:  2017        PMID: 28764012     DOI: 10.1016/j.foodchem.2017.05.080

Source DB:  PubMed          Journal:  Food Chem        ISSN: 0308-8146            Impact factor:   7.514


  17 in total

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