1979•Analytical LettersRequires access

Voltammetric and Coulometric Studies on Eugenol and Related Compounds

Masanobu Iguchi, Atsuko Nishiyama, Y. Terada, S. YAMAMURA

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Abstract

Anodic processes were studied for eugenol, isoeugenol and 2,6-dimethoxy-4-allylphenol by cyclic voltammetry at a glassy carbon electrode in methanol. Preparative electrolyses were also applied coulometrically to these phenols, followed by the separation and the determination of the structures of -e, -2e and -4e products. It was indicated that both radical and cationic reactions were controlled by the applied potentials, the solvent media and the substituents on the aromatic rings.

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Anodic processes were studied for eugenol, isoeugenol and 2,6-dimethoxy-4-allylphenol by cyclic voltammetry at a glassy carbon electrode in methanol. Preparative electrolyses were also applied coulometrically to these phenols, followed by the separation and the determination of the structures of -e, -2e and -4e products. It was indicated that both radical and cationic reactions were controlled by the applied potentials, the solvent media and the substituents on the aromatic rings.

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Available abstract

Anodic processes were studied for eugenol, isoeugenol and 2,6-dimethoxy-4-allylphenol by cyclic voltammetry at a glassy carbon electrode in methanol. Preparative electrolyses were also applied coulometrically to these phenols, followed by the separation and the determination of the structures of -e, -2e and -4e products. It was indicated that both radical and cationic reactions were controlled by the applied potentials, the solvent media and the substituents on the aromatic rings.

Key concepts: Chemistry, Isoeugenol, Eugenol, Coulometry, Phenols, Cyclic voltammetry, Acetonitrile, Organic chemistry

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