Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/160247
Title: Oxidation of capsaicin in acetonitrile in dry and wet conditions
Authors: Chan, Kwok Kiong
Muhammad Shafique Hamid
Webster, Richard David
Keywords: Science::Chemistry
Issue Date: 2021
Source: Chan, K. K., Muhammad Shafique Hamid & Webster, R. D. (2021). Oxidation of capsaicin in acetonitrile in dry and wet conditions. Journal of Electroanalytical Chemistry, 903, 115838-. https://dx.doi.org/10.1016/j.jelechem.2021.115838
Project: RG3/19 
Journal: Journal of Electroanalytical Chemistry 
Abstract: An electrochemical study of the phenol capsaicin (CAPH), the active ingredient in chilli pepper, was performed in dried and wet acetonitrile on a glassy carbon electrode. Under dried conditions, two oxidation peaks at ca. 0.7 vs. (Fc/Fc+)/V (labelled E1) and 1.0 vs. (Fc/Fc+)/V (labelled E2) and two reduction peaks at ca. 0.1 and −0.5 vs. (Fc/Fc+)/V when the scan direction was reversed were observed. Rotating disk electrode experiments indicated that the two oxidation processes occur by same number of electrons and it is proposed they occur in two one-electron steps. As water was added to the acetonitrile, hydrogen bonding interactions between the water and the phenolic groups led to the E1 and E2 potentials shifting progressively more negatively. The shift in E2 as water was added was greater than the shift in E1, so that after the addition of approximately 0.2 M H2O, only one voltammetric wave was observed (labelled as E1′) corresponding to a two-electron oxidation, that continued to shift more negatively as more water was added. Under very wet conditions ([H2O] > 1 M), only one chemically irreversible oxidation peak was observed (E1′) at ca. > 0.5 vs. (Fc/Fc+)/V with one reduction peak at ca. −0.1 vs. (Fc/Fc+)/V upon reversal of the scan direction. Controlled-potential electrolysis under wet conditions indicated a total of two-electrons per molecule were transferred with the overall mechanism interpreted as a −2e–/−H+ oxidation, followed by a hydrolysis reaction and loss of a methoxy group to form a 1,2-benzoquinone moiety.
URI: https://hdl.handle.net/10356/160247
ISSN: 1572-6657
DOI: 10.1016/j.jelechem.2021.115838
Schools: School of Physical and Mathematical Sciences 
Rights: © 2021 Elsevier B.V. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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