Electrochemical Oxidation of Quercetin

Detalhes bibliográficos
Autor(a) principal: Brett, Ana Maria Oliveira
Data de Publicação: 2003
Outros Autores: Ghica, Mariana-Emilia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/8295
https://doi.org/10.1002/elan.200302800
Resumo: The mechanism of electrochemical oxidation of quercetin on a glassy carbon electrode has been studied using cyclic, differential pulse and square-wave voltammetry at different pH. It proceeds in a cascade mechanism, related with the two catechol hydroxyl groups and the other three hydroxyl groups which all present electroactivity, and the oxidation is pH dependent. Quercetin also adsorbs strongly on the electrode surface; and the final oxidation product is not electroactive and blocks the electrode surface. The oxidation of the catechol 3prime,4prime-dihydroxyl electron-donating groups, occurs first, at very low positive potentials, and is a two electron two proton reversible reaction. The hydroxyl group oxidized next was shown to undergo an irreversible oxidation reaction, and this hydroxyl group can form a intermolecular hydrogen bond with the neighboring oxygen. The other two hydroxyl groups also have an electron donating effect and their oxidation is reversible.
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spelling Electrochemical Oxidation of QuercetinThe mechanism of electrochemical oxidation of quercetin on a glassy carbon electrode has been studied using cyclic, differential pulse and square-wave voltammetry at different pH. It proceeds in a cascade mechanism, related with the two catechol hydroxyl groups and the other three hydroxyl groups which all present electroactivity, and the oxidation is pH dependent. Quercetin also adsorbs strongly on the electrode surface; and the final oxidation product is not electroactive and blocks the electrode surface. The oxidation of the catechol 3prime,4prime-dihydroxyl electron-donating groups, occurs first, at very low positive potentials, and is a two electron two proton reversible reaction. The hydroxyl group oxidized next was shown to undergo an irreversible oxidation reaction, and this hydroxyl group can form a intermolecular hydrogen bond with the neighboring oxygen. The other two hydroxyl groups also have an electron donating effect and their oxidation is reversible.2003info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/8295http://hdl.handle.net/10316/8295https://doi.org/10.1002/elan.200302800engElectroanalysis. 15:22 (2003) 1745-1750Brett, Ana Maria OliveiraGhica, Mariana-Emiliainfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-09-01T09:18:12Zoai:estudogeral.uc.pt:10316/8295Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:42.353722Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Electrochemical Oxidation of Quercetin
title Electrochemical Oxidation of Quercetin
spellingShingle Electrochemical Oxidation of Quercetin
Brett, Ana Maria Oliveira
title_short Electrochemical Oxidation of Quercetin
title_full Electrochemical Oxidation of Quercetin
title_fullStr Electrochemical Oxidation of Quercetin
title_full_unstemmed Electrochemical Oxidation of Quercetin
title_sort Electrochemical Oxidation of Quercetin
author Brett, Ana Maria Oliveira
author_facet Brett, Ana Maria Oliveira
Ghica, Mariana-Emilia
author_role author
author2 Ghica, Mariana-Emilia
author2_role author
dc.contributor.author.fl_str_mv Brett, Ana Maria Oliveira
Ghica, Mariana-Emilia
description The mechanism of electrochemical oxidation of quercetin on a glassy carbon electrode has been studied using cyclic, differential pulse and square-wave voltammetry at different pH. It proceeds in a cascade mechanism, related with the two catechol hydroxyl groups and the other three hydroxyl groups which all present electroactivity, and the oxidation is pH dependent. Quercetin also adsorbs strongly on the electrode surface; and the final oxidation product is not electroactive and blocks the electrode surface. The oxidation of the catechol 3prime,4prime-dihydroxyl electron-donating groups, occurs first, at very low positive potentials, and is a two electron two proton reversible reaction. The hydroxyl group oxidized next was shown to undergo an irreversible oxidation reaction, and this hydroxyl group can form a intermolecular hydrogen bond with the neighboring oxygen. The other two hydroxyl groups also have an electron donating effect and their oxidation is reversible.
publishDate 2003
dc.date.none.fl_str_mv 2003
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/8295
http://hdl.handle.net/10316/8295
https://doi.org/10.1002/elan.200302800
url http://hdl.handle.net/10316/8295
https://doi.org/10.1002/elan.200302800
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Electroanalysis. 15:22 (2003) 1745-1750
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