Electrochemical Characterization of Sulfide Tagging via Its Reaction with Benzoquinone Derivatives
Debora Giovanelli, Nathan S. Lawrence, Li Jiang, Timothy G. J. Jones, Richard G. Compton
Abstract
Debora Giovanelli, Nathan S. Lawrence, Li Jiang, Timothy G. J. Jones, Richard G. Compton
Abstract
The voltammetric response of a range of structurally diverse substituted benzoquinones species (p-benzoquinone, 2,3-dimethoxy- 5-methyl-p-benzoquinone, 2,6-dimethoxy-p-benzoquinone, and 3,5-ditert-butyl-o-benzoquinone) to increasing additions of sulfide has been examined using square wave voltammetry. In all cases the response shows that the quinone undergoes a reaction with sulfide to form a new redox active species. It is shown that by judicious choice of the pH of the solution analytical signals can be obtained for each species; the corresponding analytical parameters are detailed and the results critically appraised.
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The voltammetric response of a range of structurally diverse substituted benzoquinones species (p-benzoquinone, 2,3-dimethoxy- 5-methyl-p-benzoquinone, 2,6-dimethoxy-p-benzoquinone, and 3,5-ditert-butyl-o-benzoquinone) to increasing additions of sulfide has been examined using square wave voltammetry. In all cases the response shows that the quinone undergoes a reaction with sulfide to form a new redox active species. It is shown that by judicious choice of the pH of the solution analytical signals can be obtained for each species; the corresponding analytical parameters are detailed and the results critically appraised.
Key concepts: Chemistry, Benzoquinone, Quinone, Sulfide, Redox, Electrochemistry, 1,4-Benzoquinone, Cyclic voltammetry