通过快速和选择性的二次插入,通过催化烯酸盐聚合物化中抑制链转移
Zhongbao Jian1, Moritz C Baier, Stefan Mecking
1Chair of Chemical Materials Science, Department of Chemistry, University of Konstanz , Universitätsstrasse 10, 78457 Konstanz, Germany.
Journal of the American Chemical Society
|February 13, 2015
概括
在共聚合过程中,链转移是通过快速连续插入烯酸无水化物来解决的. 这种方法通过形成循环单元和初级基团来增强共聚物分子重量,改善链的生长.
科学领域:
- 聚合物化学 聚合物化学
- 有机合成 有机合成
- 材料科学 材料科学 材料科学
背景情况:
- 催化共聚化通常在结合极性乙烯基单体后遭受不必要的链转移.
- 这种链接转移限制了可实现的分子量和对聚合物架构的控制.
研究的目的:
- 提出一种新的方法来克服催化共聚合过程中的链转移.
- 通过使用特定的单体战略来增强共聚合物分子重量.
主要方法:
- 在催化共聚合中使用烯酸化物作为单体.
- 使用快速,连续的分子内插入机制.
主要成果:
- 烯酸无水化物经历快速的分子内插入,形成一个循环重复单元 (>96%).
- 这一过程产生了一个主要的基组,有利于连锁链的持续生长.
- 与使用单功能烯酸单体相比,实现了显著增强的共聚物分子重量.
结论:
- 快速连续插入的烯酸无水化物有效地抑制了不必要的链转移.
- 这一策略为具有受控结构的高分子量共聚合物提供了一条可行的途径.
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