Issue 9, 1995

Aminoxyl functionalized polythiophene: synthesis and electrochemical applications

Abstract

2,2,6,6-Tetramethyl-4-[4-(3-thienyl)butoxycarbonyl]piperidin-1-yloxyl and the corresponding N-hydroxytosylate salt have been prepared and polymerized in good yields by chemical and electrochemical methods. The chemically prepared tetramethylpiperidin-1-yloxyl (TEMPO)-substituted polythiophenes had electronic conductivities, when doped with iodine, of ca. 10–3 S cm–1 and were paramagnetic. Electrochemically deposited polymers showed reversible waves at 0.59 V vs. Ag/AgCl in their cyclic voltammograms. Preparative-scale experiments with a platinum electrode coated with electrodeposited polymer showed that efficient oxidation of 4-methoxybenzyl alcohol to 4-methoxybenzaldehyde could be achieved by a much lower potential to that required without mediation.

Article information

Article type
Paper

J. Mater. Chem., 1995,5, 1291-1295

Aminoxyl functionalized polythiophene: synthesis and electrochemical applications

A. Iragi, J. A. Crayston, J. C. Walton and A. Harrison, J. Mater. Chem., 1995, 5, 1291 DOI: 10.1039/JM9950501291

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