Monitoring of intermediates of clioquinol electro-oxidation by thin-layer spectral and electrophoretic electrochemistry

• A combination of thin-layer spectral and electrophoretic electrochemistry.
• Four products including two intermediates were separated by electrophoresis.
• Disproportionation was followed by double-wavelength cyclic voltabsorptometry.
• A complex EC mechanism is proposed for oxidation of clioquinol.

Monitoring of unstable intermediates is very important for clarifying complex electrochemical reaction pathways. A combination of thin-layer spectral and electrophoretic electrochemistry, both based on fast thin-layer electrolysis, has been developed to monitor the intermediates of electro-oxidation of clioquinol in acidic, physiological and alkaline buffer media. Two thin-layer electrochemical cells were fabricated and coupled with a UV-vis spectrometer and an electrophoresis apparatus, respectively. Double-potential thin-layer UV–vis spectroelectrochemistry, double-wavelength thin-layer cyclic voltabsorptometry and thin-layer electrophoretic electrochemistry provided mutually-supporting information on the redox pathway of clioquinol. Two intermediates, a disproportionatable semiquinone anion radical and a labile quinone derivative, were detected. The chemical activity of the semiquinone anion radical is highly pH-dependent. The final soluble products of clioquinol are pH-dependent but irrelevant to whether the oxidation reaction is electrochemical or chemical in nature. A complex reaction pathway is proposed for the oxidation of clioquinol, which may help to better understand the metabolism mechanism and chemical toxicity of this anti-neurodegeneration drug.

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