Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/11713
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dc.contributor.authorIvanovic, Nenad-
dc.contributor.authorJovanović, Ljiljana-
dc.contributor.authorMarković, Zoran-
dc.contributor.authorMarković, Violeta-
dc.contributor.authorJoksović, Milan-
dc.contributor.authorMilenkovic, Dejan-
dc.contributor.authorDjurdjevic, Predrag-
dc.contributor.authorCiric, Andrija-
dc.contributor.authorJoksović, Ljubinka-
dc.date.accessioned2021-04-20T19:02:48Z-
dc.date.available2021-04-20T19:02:48Z-
dc.date.issued2016-08-16-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/11713-
dc.description.abstract© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Nine 1,2,4-triazole-3-thiones containing phenolic acid moiety have been synthesized and examined by scavenging of stable DPPH (2,2-diphenyl-1-picrylhydrazyl) radical, measurement of reducing capacity, cyclic voltammetry experiments and density functional theory (DFT). The differences in DPPH-radical scavenging activity of the compounds 4 a-i are affected by the stability of the corresponding radicals or radical cations and possibility of delocalization of unpaired electron through benzene and triazole ring. Significantly, lower proton affinity (PA) values than bond dissociation enthalpy (BDE) indicate SPLET (sequential proton loss electron transfer) mechanism under these experimental conditions.-
dc.relation.ispartofChemistrySelect-
dc.titlePotent 1,2,4-Triazole-3-thione Radical Scavengers Derived from Phenolic Acids: Synthesis, Electrochemistry, and Theoretical Study-
dc.typejournal article-
dc.identifier.doi10.1002/slct.201600738-
dc.identifier.scopus85010327021-
Appears in Collections:Faculty of Science, Kragujevac
Institute for Information Technologies, Kragujevac

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