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dc.creatorHENRIQUEZ,CAROLA
dc.creatorALIAGA,CAROLINA
dc.creatorLISSI,EDUARDO
dc.date2004-03-01
dc.date.accessioned2020-02-17T15:32:12Z
dc.date.available2020-02-17T15:32:12Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0717-97072004000100011
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/130071
dc.descriptionThe kinetic profile associated to the reaction of phenols with 2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) derived radicals is extremely dependent of the characteristics of the substrate. In particular, polyphenols present complex profiles that can be associated to successive reactions of different reactive centers present in the target molecule. Also, changes in the secondary reactions of the produced radicals can lead to a partial recovery of the ABTS radical concentration at intermediate reaction times, as observed employing 1,4-dihydroxybenzene. Although the kinetic profiles of monophenols are considerably simpler, the stoichiometry of the process is unexpected. For example, the data obtained imply that four radicals are consumed by each p-tertbutylphenol molecule introduced into the system. This large stoichiometric coefficient is not compatible with a simple, phenol promoted, back reduction of the ABTS radical. These results, as well as the overshoot observed employing 1,4-dihydroxybencene, cast doubts on the use of ABTS based methodologies to quantitatively measure the capacity of a given compound to trap free radicals or the amount of free radical scavengers present in complex mixtures
dc.formattext/html
dc.languageen
dc.publisherSociedad Chilena de Química
dc.relation10.4067/S0717-97072004000100011
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceJournal of the Chilean Chemical Society v.49 n.1 2004
dc.subjectABTS
dc.subjectphenols
dc.subjectantioxidant capacities
dc.subjectfree radical scavenging
dc.titleKINETICS PROFILES IN THE REACTION OF ABTS DERIVED RADICALS WITH SIMPLE PHENOLS AND POLYPHENOLS


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