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Electrocatalytic chirality on magneto-electropolymerized polyaniline electrodes

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Abstract

Chiral polyaniline electrodes were prepared by the magneto-electropolymerization (MEP) method. Cyclic voltammograms (CVs) of l-ascorbic acid (L-AA), d-isoascorbic acid (D-AA), and l-3-(3,4-dihydroxyphenyl)alanine were measured on the MEP polyaniline electrodes and their electrode reactions were electrocatalytic. The CV peak currents varied depending on the chirality of the polyaniline and the optically active species, while the peak potentials were independent of the chirality. The CVs of L-AA and D-AA were also measured on a Pt electrode in a (−)-camphor-10-sulfonic acid supporting electrolyte solution, and the chiral behavior was observed in the peak potentials. It is considered that the electrocatalytic process is responsible for the chiral electrochemical behavior on the polyaniline electrodes.

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Acknowledgement

The MEP experiments with a cryocooled superconducting magnet were performed in the High Field Laboratory for Superconducting Materials, Institute for Materials Research Tohoku University. This work was partly supported by a Grant-In-Aid of Scientific Research for Priority Area (area 767) from the Ministry of Education, Culture, Sports, Science and Technology of Japan.

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Correspondence to Iwao Mogi.

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Contribution to special issue on “Magnetic field effects in Electrochemistry”.

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Mogi, I., Watanabe, K. Electrocatalytic chirality on magneto-electropolymerized polyaniline electrodes. J Solid State Electrochem 11, 751–756 (2007). https://doi.org/10.1007/s10008-006-0191-2

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  • DOI: https://doi.org/10.1007/s10008-006-0191-2

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