Electrochemical synthesis of polyaniline in the presence of poly (amidosulfonic acid)s with different rigidity of polymer backbone and characterization of the films obtained

被引:35
|
作者
Nekrasov, A. A. [1 ]
Gribkova, O. L. [1 ]
Eremina, T. V. [2 ]
Isakovaa, A. A. [1 ]
Ivanov, V. F. [1 ]
Tverskoj, V. A. [2 ]
Vannikov, A. V. [1 ]
机构
[1] Russian Acad Sci, AN Frumkin Inst Phys Chem & Electrochem, Moscow 119991, Russia
[2] MV Lomonosov State Acad Fine Chem Technol, Moscow 117571, Russia
关键词
polyaniline; spectroelectrochemistry; matrix synthesis; conducting polymers;
D O I
10.1016/j.electacta.2007.08.060
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We have studied electrochemical matrix polymerization of aniline in the presence of poly(amidosulfonic acid)s of different nature: poly(2-acrylamido-2-methyl-1-propanosulfonic acid) (PAMPSA, flexible backbone); poly (p,p'-(2,2'-disulfoacid)-diphenylene-iso-phthalamid) (i-PASA, semi-rigid backbone); poly(p,p'-(2,2'-disulfoacid)-diphelylene-tore-phthalamid) (t-PASA, rigid backbone). Also, we have investigated spectral and electrochemical properties of the films obtained, as well as their surface morphology. The matrix polymerization results in the formation of interpolymer complexes of polyaniline (PANT) and the above-cited polyacids. The acceleration of aniline electropolymerization in the presence of poly(amidosulfonic acid)s was observed due to association of aniline molecules to sulfonic groups of the polyacid and higher local concentration of protons near the polyacid backbone. The rigid-chain polyacids interfere with the normal course of the electropolymerization, which manifests itself in the changes of the shape of time dependences of absorbance and charge. Cyclic voltammetry and spectroelectrochemical experiments showed that the formation of interpolymer complex with rigid-chain polyacids distorts spectroelectrochemical characteristics of PANI. This evidently results from steric hindrances in the formation of quinoid units. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3789 / 3797
页数:9
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