POLYMERIZATION OF DIPHENYL DISULFIDE BY THE S-S BOND-CLEAVAGE WITH A LEWIS ACID - A NOVEL PREPARATION ROUTE TO POLY(PARA-PHENYLENE SULFIDE)

被引:53
作者
TSUCHIDA, E
YAMAMOTO, K
NISHIDE, H
YOSHIDA, S
JIKEI, M
机构
[1] Department of Polymer Chemistry, Waseda University
关键词
D O I
10.1021/ma00210a001
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(p-phenylene sulfide) (PPS) is efficiently and conveniently produced by a cationic and oxidative polymerization. Diphenyl disulfide is allowed to react with a Lewis acid such as antimony pentachloride at room temperature and is polymerized to PPS. The polymer is isolated as a white powder, whose 1,4 structure is confirmed by IR. Phenylbis(phenylthio)sulfonium ion acts as an active species, which is formed by oxidation of the S-S bond of diphenyl disulfide with the Lewis acid, and is electrophilically substituted on the phenyl ring. The polymerization mechanism is discussed and compared to a model reaction using dimethyl disulfide. © 1990, American Chemical Society. All rights reserved.
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页码:2101 / 2106
页数:6
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