感应效应辅助的链增长聚凝. 从具有低多分散性的甲基替代性芳香聚胺转为甲基替代性芳香聚胺的合成发展
Ryuji Sugi1, Akihiro Yokoyama, Taniyuki Furuyama
1Department of Applied Chemistry, Kanagawa University, Rokkakubashi, Kanagawa-ku, Yokohama 221-8686, Japan.
Journal of the American Chemical Society
|July 21, 2005
概括
研究人员开发了一种用于元替代单体的新链增长聚凝方法,使得精确定义的聚合物和具有狭窄分子量分布的块共聚合物的受控合成成为可能.
科学领域:
- 聚合物化学 聚合物化学
- 有机合成 有机合成
背景情况:
- 开发对元置换单体的受控聚合方法是具有挑战性的.
- 现有的方法往往导致不必要的自我凝结.
研究的目的:
- 扩展精确定义的凝结聚合物合成从帕-到元替代的单体.
- 为了研究m-(octylamino) 酸的链增长聚凝.
主要方法:
- 研究了m-(octylamino) 酸 Ester的多重凝结,使用强基,如六甲基二甲基化 (LiHMDS).
- 使用了诸如基酸盐和4-甲基酸盐之类的启动剂.
- 在区块共聚合物合成中采用单体添加法.
主要成果:
- 乙烯单体 (1b) 聚合是通过链式聚合而没有自我凝结进行的.
- 聚合物分子重量 (Mn) 与单体与启动器的比率线性增加.
- 获得了狭窄的分子量分布 (Mw/Mn).
- 成功合成了N-化聚胺和聚胺的块共聚合物.
结论:
- 实现了对甲基替代胺聚合物的受控链增长聚凝.
- 证明了明确定义的聚合物和块共聚合物的合成.
- 开发的方法为创建先进的聚合物架构提供了一条途径.
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