Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/20137
Title: Phenol And Para-Substituted Phenols Electrochemical Oxidation Pathways
Authors: Enache, Teodor Adrian 
Brett, Ana Maria Oliveira 
Keywords: Phenol; Para-substituted phenols; Voltammetry; Oxidation; Glassy carbon
Issue Date: 2011
Publisher: Elsevier
Citation: ENACHE, Adrian Enache; OLIVEIRA-BRETT, Ana Maria - Phenol and para-substituted phenols electrochemical oxidation pathways. "Journal of Electroanalytical Chemistry". ISSN 1572-6657. 655:1 (2011) 9-16
Serial title, monograph or event: Journal of Electroanalytical Chemistry
Volume: 655
Issue: 1
Abstract: The electrochemical behaviour of phenol, catechol, hydroquinone, resorcinol, dopamine, and para-substituted phenolic compounds, 4-ethylphenol, tyrosine, and tyramine, was studied over a wide pH range using a glassy carbon electrode. The oxidation of phenol is pH dependent and irreversible, occurring in one step, and followed by hydrolyse in ortho- and para- positions, leading to two oxidation products, catechol and hydroquinone. The oxidation of phenol oxidation products, ortho-phenol and para-phenol, is reversible and pH dependent. The oxidation potential of parasubstituted phenols varies slightly due to their substituent group in position C4, and occurs in one oxidation step corresponding to the oxidation of phenol. The oxidation products of this group of para-substituted phenols are reversibly oxidised and adsorb on the electrode surface.
URI: http://hdl.handle.net/10316/20137
ISSN: 1572-6657
DOI: 10.1016/j.jelechem.2011.02.022
Rights: openAccess
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais

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