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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/527
DC FieldValueLanguage
dc.contributor.authorNakarada, Đuraen_US
dc.contributor.authorPejin, Borisen_US
dc.contributor.authorDimić, Dušanen_US
dc.contributor.authorIvanović-Šašić, Anaen_US
dc.contributor.authorMojović, Zoricaen_US
dc.contributor.authorMojović, Milošen_US
dc.date.accessioned2022-12-15T16:09:25Z-
dc.date.available2022-12-15T16:09:25Z-
dc.date.issued2019-06-15-
dc.identifier.issn1878-5190en
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/527-
dc.description.abstractThe electrochemistry of catecholamine neurotransmitters and their precursor l-dopa has been widely studied due to their relevance as biologically important compounds. The detection of these compounds from aqueous solution is hindered by the coexistence of quinone or hydroquinone. However, it was suggested that quinones adsorbed on the electrode surface can enhance catechol detection. In order to estimate the degree of interaction between quinones and l-dopa, cyclic voltammetry and UV–Vis spectroscopic study was performed. A sesquiterpenoid hydroquinone, isolated from the marine sponge Dysidea avara (avarol), has been used in this study. The change of apparent heterogeneous rate constant with different avarol/l-dopa ratio indicated that charge transfer could be enhanced at some extent. In addition to this, the obtained results for avarol and hydroquinone (its structural element) were compared. UV–Vis spectroscopic analysis confirmed interaction between l-dopa and avarol or hydroquinone. Taken all together, the interaction of l-dopa was stronger with hydroquinone than with avarol, presumably reflecting the conformational restrains of avarol caused by its terpenoid moiety.en
dc.relation.ispartofReaction Kinetics, Mechanisms and Catalysisen
dc.subjectAvarolen
dc.subjectCyclic voltammetryen
dc.subjectHydroquinoneen
dc.subjectl-dopaen
dc.subjectUV–Visen
dc.titleElectrochemical and spectroscopic study of l-dopa interaction with avarolen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s11144-019-01575-z-
dc.identifier.scopus2-s2.0-85064334278-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85064334278-
dc.relation.firstpage219en
dc.relation.lastpage229en
dc.relation.issue1en
dc.relation.volume127en
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.grantfulltextnone-
crisitem.author.orcid0000-0002-0154-6430-
crisitem.author.orcid0000-0001-8127-5396-
crisitem.author.orcid0000-0002-1868-9913-
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University of Belgrade
Faculty of Physical Chemistry
Studentski trg 12-16
11158 Belgrade 118
PAC 105305
SERBIA
University of Belgrade Faculty of Physical Chemistry