ELECTROCHEMICAL POLYMERIZATION OF 3-OCTYLPYRROLE

被引:30
作者
MASUDA, H
TANAKA, S
KAERIYAMA, K
机构
[1] RES INST POLYMERS & TEXT,1-1-4 TSUKUBA CITY,TSUKUBA,IBARAKI 305,JAPAN
[2] IND RES INST,KANAZAWA KU,YOKOHAMA 236,JAPAN
关键词
D O I
10.1002/pola.1990.080280715
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Electrochemical polymerization of 3‐octylpyrrole (OCPY) yielded a film on the anode. Its conductivity was 5 S/cm. Infrared spectra of OCPY and poly(3‐octylpyrrole) (POCPY) were compared with those of related monomers and polymers, and as a result, the pyrrole rings appeared quite likely linked at 2‐ and 5‐positions. Cyclic voltammograms of a PF–6‐doped POCPY film had an anodic peak at 0.16 V vs. Ag and a cathodic peak at 0.12 V. Doped POCPY was stable and soluble in such polar solvents as tetrahydrofuran, N‐methylpyrrolidinone and pyridine. Although the absorption spectrum of the film had three peaks at 1.0, 2.5 and 3.6 eV, as also in the case of poly(3‐methylpyrrole), the spectra in pyridine and THF solutions indicated two peaks at 1.9 and 3.2 eV. Scanning electron microscopy (SEM) showed the POCPY films to have a unique morphology, depending on the electrolytes used for electrochemical polymerization. The introduction of an octyl group made polypyrrole soluble in organic solvents, but effective conjugation length became shorter and the texture of films rougher. Copyright © 1990 John Wiley & Sons, Inc.
引用
收藏
页码:1831 / 1840
页数:10
相关论文
共 18 条
[1]   FORCE-FIELD OF THE PYRROLE MOLECULE CALCULATED BY AN ITERATIVE AUTO-COHERENT METHOD [J].
ACEVEDOGONZALEZ, CA ;
CAMPOSVALLETTE, M ;
CLAVIJOCAMPOS, RE .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 1986, 42 (08) :919-925
[2]   HIGHLY CONDUCTING POLYPARAPHENYLENE, POLYPYRROLE, AND POLYTHIOPHENE CHAINS - AN ABINITIO STUDY OF THE GEOMETRY AND ELECTRONIC-STRUCTURE MODIFICATIONS UPON DOPING [J].
BREDAS, JL ;
THEMANS, B ;
FRIPIAT, JG ;
ANDRE, JM ;
CHANCE, RR .
PHYSICAL REVIEW B, 1984, 29 (12) :6761-6773
[3]   SOLUBLE, CONDUCTING POLYMERS FROM 3-SUBSTITUTED THIOPHENES AND PYRROLES [J].
BRYCE, MR ;
CHISSEL, A ;
KATHIRGAMANATHAN, P ;
PARKER, D ;
SMITH, NRM .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1987, (06) :466-467
[4]   SELF-DOPED WATER-SOLUBLE CONDUCTING POLYMERS [J].
HAVINGA, EE ;
VANHORSSEN, LW ;
TENHOEVE, W ;
WYNBERG, H ;
MEIJER, EW .
POLYMER BULLETIN, 1987, 18 (03) :277-281
[5]  
KAERIYAMA K, 1989, MAKROMOL CHEM-RAPID, V10, P171
[6]  
KAERIYAMA K, 1989, SYNTHETIC MET, V28, pC611, DOI 10.1016/0379-6779(89)90581-X
[7]   SOLUBLE CONDUCTING POLYPYRROLE - POLY(3-OCTYLPYRROLE) [J].
MASUDA, H ;
TANAKA, S ;
KAERIYAMA, K .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1989, (11) :725-726
[8]  
MASUDA H, IN PRESS SYNTH MET
[9]  
MASUDA H, IN PRESS
[10]  
MASUDA H, 1989, SYNTHETIC MET, V32, P29