Thermal isomerization of cis-poly(phenylacetylene). Scission of polymer main-chain and formation of 1,3,5-triphenylbenzene as a pyrolysis product

被引:18
作者
Matsunami, S
Watanabe, T
Kamimura, H
Kakuchi, T
Ishii, F
Tsuda, K
机构
[1] HOKKAIDO UNIV,GRAD SCH ENVIRONM EARTH SCI,SAPPORO,HOKKAIDO 060,JAPAN
[2] HOKKAIDO UNIV,FAC ENGN,SAPPORO,HOKKAIDO 060,JAPAN
[3] ASAHIKAWA NATL COLL TECHNOL,DEPT IND CHEM,ASAHIKAWA,HOKKAIDO 071,JAPAN
关键词
poly(phenylacetylene); cis-trans isomerization; rhodium complex catalyst;
D O I
10.1016/S0032-3861(96)00383-7
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
After cis-poly(phenylacetylene)s (cis-PPAs) were heated at 180 degrees C for 1 h, the M(n)s decreased from 5000-53 000 to 2000-2600, 1,3,5-TPB corresponding to the cyclic trimer of phenylacetylene was formed, and the yields of the annealed PPA and 1,3,5-triphenylbenzene (1,3,5-TPB) did not significantly vary. A peak at 280 nm due to the phenyl ring and broad band up to 600 nn due to the pi-pi* transition of the main-chain were observed in the u.v./vis. spectrum of cis-PPA. On the other hand, the absorption due to the conjugated main-chain disappeared for annealed PPA, though the phenyl group absorption was detected. The disappearance of the main-chain absorption can be explained by deflection of the main-chain. Copyright (C) 1996 Elsevier Science Ltd.
引用
收藏
页码:4853 / 4855
页数:3
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