Electrochemical properties and Fourier transform-infrared spectroscopic investigations of the redox behaviour of poly(indole-5-carboxylic acid) in LiClO4-acetonitrile solutions
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作者:
Billaud, D
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机构:Univ Nancy 1, LCSM, UMR 7555, F-54506 Vandoeuvre Les Nancy, France
Billaud, D
Humbert, B
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机构:Univ Nancy 1, LCSM, UMR 7555, F-54506 Vandoeuvre Les Nancy, France
Humbert, B
Thevenot, L
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机构:Univ Nancy 1, LCSM, UMR 7555, F-54506 Vandoeuvre Les Nancy, France
Thevenot, L
Thomas, P
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机构:Univ Nancy 1, LCSM, UMR 7555, F-54506 Vandoeuvre Les Nancy, France
Thomas, P
Talbi, H
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机构:Univ Nancy 1, LCSM, UMR 7555, F-54506 Vandoeuvre Les Nancy, France
Talbi, H
机构:
[1] Univ Nancy 1, LCSM, UMR 7555, F-54506 Vandoeuvre Les Nancy, France
[2] LCPE, CNRS UHP, F-54600 Villers Les Nancy, France
Electropolymerisation of indole-5-carboxylic-acid leads to the formation of electroactive polymer films. Potentiostatic deposition of the related polymer, poly(indole-5-carboxylic-acid), was carried out at a constant potential at 1.35 V versus SCE. The cyclic voltammogram of the resulting polymer in LiClO4 (0.15 mol dm(-3))/acetonitrile solution is characterized by two poorly resolved anodic and cathodic set peaks. FTIR spectroscopy was used to characterize both reduced and oxidized forms of poly(indole-5-carboxylic-acid). Assignments of the vibrational modes were proposed by comparison of the vibrational spectra of polyindole and polycyanoindole. The polymerization sites correspond to the 2 and 3 carbon positions of the pyrrole cycle. In the oxidized form of the polymer, the NH group is deprotonated while the quinoid form is present between the pyrrole rings. (C) 2002 Elsevier Science B.V. All rights reserved.