STRUCTURAL ANALYSIS AND ENVIRONMENTAL STABILITY OF POLYFLUORINATED GROUP SUBSTITUTED POLYTHIOPHENES*
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STRUCTURAL ANALYSIS AND ENVIRONMENTAL STABILITY OF POLYFLUORINATED GROUP SUBSTITUTED POLYTHIOPHENES*
Vol. 14, Issue 4, Pages: 330-337(1996)
Affiliations:
1. Shanghai Institute of Organic Chemistry
2. Chinese Academy of Sciences
3. Shanghai 200232
Author bio:
Funds:
DOI:
CLC:TQ316.3
Published:20 December 1996
Accepted:
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[1]张旭庆,沈学明,杨士勇,陆伟,张景云.STRUCTURAL ANALYSIS AND ENVIRONMENTAL STABILITY OF POLYFLUORINATED GROUP SUBSTITUTED POLYTHIOPHENES[J].Chinese Journal of Polymer Science,1996,{4}(04):330-337.
ZHANG Xuqing, SHEN Xueming, YANG Shiyong, et al. STRUCTURAL ANALYSIS AND ENVIRONMENTAL STABILITY OF POLYFLUORINATED GROUP SUBSTITUTED POLYTHIOPHENES*[J]. 1996, 14(4): 330-337.
[1]张旭庆,沈学明,杨士勇,陆伟,张景云.STRUCTURAL ANALYSIS AND ENVIRONMENTAL STABILITY OF POLYFLUORINATED GROUP SUBSTITUTED POLYTHIOPHENES[J].Chinese Journal of Polymer Science,1996,{4}(04):330-337.DOI:
ZHANG Xuqing, SHEN Xueming, YANG Shiyong, et al. STRUCTURAL ANALYSIS AND ENVIRONMENTAL STABILITY OF POLYFLUORINATED GROUP SUBSTITUTED POLYTHIOPHENES*[J]. 1996, 14(4): 330-337.DOI:
STRUCTURAL ANALYSIS AND ENVIRONMENTAL STABILITY OF POLYFLUORINATED GROUP SUBSTITUTED POLYTHIOPHENES*
<正> Electrochemical polymerization of 3-fluoroalkoxy and 3-fluoroether thiophenes givespolymers with relatively high molecular weights and good processibility. Investigationof these polymers by means of GPC indicates that an increase in the number of fluorineatoms in the fluorinated group results in a decrease in degree of polymerization of thepolymers in the same polythiophene series. As shown by NMR and FTIR
the polyfluo-rinated group substituted polythiophenes have regular 2
5-coupling in their main chains.The SEM micrographs of the polymer films exhibit that polymer (1)-poly [3-2
2
3
3-tetrafluoro-propoxy) thiophene] possesses more regular structure than the other polymersdo. Substitution of polythiophenes by fluorinated groups leads to the polymers with highelectric
electrochemical and thermal stability.
Abstract
Electrochemical polymerization of 3-fluoroalkoxy and 3-fluoroether thiophenes givespolymers with relatively high molecular weights and good processibility. Investigationof these polymers by means of GPC indicates that an increase in the number of fluorineatoms in the fluorinated group results in a decrease in degree of polymerization of thepolymers in the same polythiophene series. As shown by NMR and FTIR
the polyfluo-rinated group substituted polythiophenes have regular 2
5-coupling in their main chains.The SEM micrographs of the polymer films exhibit that polymer (1)-poly [3-2
2
3
3-tetrafluoro-propoxy) thiophene] possesses more regular structure than the other polymersdo. Substitution of polythiophenes by fluorinated groups leads to the polymers with highelectric
electrochemical and thermal stability.
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