Solid State Electrochemical Oxidation Mechanisms Of Morin in Aqueous Media

Detalhes bibliográficos
Autor(a) principal: Janeiro, Patricia
Data de Publicação: 2005
Outros Autores: Brett, Ana Maria Oliveira
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/8284
https://doi.org/10.1002/elan.200403155
Resumo: The mechanism of electrochemical oxidation of morin has been studied using cyclic, differential pulse and square-wave voltammetry techniques in aqueous electrolyte with solid, insoluble morin hydrate mechanically transferred to a glassy carbon electrode surface, over a wide pH range. The oxidation mechanism proceeds in sequential steps, related with the hydroxyl groups in the three aromatic rings and the oxidation is pH dependent over part of the pH range the oxidation potentials are shifted to lower values with increasing pH. Oxidation of the 2prime,4primedihydroxy moiety at the B ring of morin occurs first, at very low positive potentials, and is a one electron one proton reversible reaction. The hydroxyl groups oxidized at more positive potentials were shown to undergo an irreversible oxidation reaction.
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spelling Solid State Electrochemical Oxidation Mechanisms Of Morin in Aqueous MediaThe mechanism of electrochemical oxidation of morin has been studied using cyclic, differential pulse and square-wave voltammetry techniques in aqueous electrolyte with solid, insoluble morin hydrate mechanically transferred to a glassy carbon electrode surface, over a wide pH range. The oxidation mechanism proceeds in sequential steps, related with the hydroxyl groups in the three aromatic rings and the oxidation is pH dependent over part of the pH range the oxidation potentials are shifted to lower values with increasing pH. Oxidation of the 2prime,4primedihydroxy moiety at the B ring of morin occurs first, at very low positive potentials, and is a one electron one proton reversible reaction. The hydroxyl groups oxidized at more positive potentials were shown to undergo an irreversible oxidation reaction.2005info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/8284http://hdl.handle.net/10316/8284https://doi.org/10.1002/elan.200403155engElectroanalysis. 17:9 (2005) 733-738Janeiro, PatriciaBrett, Ana Maria Oliveirainfo: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:RCAAP2020-05-25T13:16:07Zoai:estudogeral.uc.pt:10316/8284Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:42.958814Repositório 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 Solid State Electrochemical Oxidation Mechanisms Of Morin in Aqueous Media
title Solid State Electrochemical Oxidation Mechanisms Of Morin in Aqueous Media
spellingShingle Solid State Electrochemical Oxidation Mechanisms Of Morin in Aqueous Media
Janeiro, Patricia
title_short Solid State Electrochemical Oxidation Mechanisms Of Morin in Aqueous Media
title_full Solid State Electrochemical Oxidation Mechanisms Of Morin in Aqueous Media
title_fullStr Solid State Electrochemical Oxidation Mechanisms Of Morin in Aqueous Media
title_full_unstemmed Solid State Electrochemical Oxidation Mechanisms Of Morin in Aqueous Media
title_sort Solid State Electrochemical Oxidation Mechanisms Of Morin in Aqueous Media
author Janeiro, Patricia
author_facet Janeiro, Patricia
Brett, Ana Maria Oliveira
author_role author
author2 Brett, Ana Maria Oliveira
author2_role author
dc.contributor.author.fl_str_mv Janeiro, Patricia
Brett, Ana Maria Oliveira
description The mechanism of electrochemical oxidation of morin has been studied using cyclic, differential pulse and square-wave voltammetry techniques in aqueous electrolyte with solid, insoluble morin hydrate mechanically transferred to a glassy carbon electrode surface, over a wide pH range. The oxidation mechanism proceeds in sequential steps, related with the hydroxyl groups in the three aromatic rings and the oxidation is pH dependent over part of the pH range the oxidation potentials are shifted to lower values with increasing pH. Oxidation of the 2prime,4primedihydroxy moiety at the B ring of morin occurs first, at very low positive potentials, and is a one electron one proton reversible reaction. The hydroxyl groups oxidized at more positive potentials were shown to undergo an irreversible oxidation reaction.
publishDate 2005
dc.date.none.fl_str_mv 2005
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/8284
http://hdl.handle.net/10316/8284
https://doi.org/10.1002/elan.200403155
url http://hdl.handle.net/10316/8284
https://doi.org/10.1002/elan.200403155
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Electroanalysis. 17:9 (2005) 733-738
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