Two different reaction mechanisms of cinnamate side groups attached to the various polymer backbones

被引:39
作者
Sung, SJ
Cho, KY
Hah, H
Lee, J
Shim, HK
Park, JK
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Taejon, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Chem, Taejon, South Korea
[3] Korea Adv Inst Sci & Technol, Sch Mol Sci BK21, Taejon, South Korea
关键词
cinnamate; polymer flexibility; thermal crosslinking;
D O I
10.1016/j.polymer.2006.02.003
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Cinnamate polymers are well known photoreactive polymers due to [2 + 2] cycloaddition reaction of cinnamate side group. In this work, we have found that the cinnamate side groups could be also reacted by thermal energy, and this reaction is presumed to attribute to the radical reaction of carbon double bond in the cinnamate groups. Contrary to the photocycloaddition reaction of the cinnamate side groups, the thermal reaction of cinnamate side group was closely related to the flexibility of polymer backbone. The difference of the mechanism between the photocycloaddition reaction and thermal crosslinking reaction was confirmed by H-1 NMR and C-13 NMR analysis of the model compound. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2314 / 2321
页数:8
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