生物催化环开放的多聚化morpholinones:功能化聚的新策略
Timothy R Blake1, Robert M Waymouth
1Department of Chemistry, Stanford University , Stanford, California 94306, United States.
Journal of the American Chemical Society
|June 20, 2014
概括
研究人员开发了一种新方法来合成N替代的-2-,从而通过有机催化环开放聚合制造功能化的多氨基. 聚合的成功取决于原子的杂交,在去除保护后产生阴离子聚合物.
科学领域:
- 有机化学 有机化学
- 聚合物化学 聚合物化学
- 催化剂是一种催化剂.
背景情况:
- 替代N的Morpholin-2-ones是异环乳,在聚合物合成中具有潜在的应用.
- 乳的环开聚合 (ROP) 是生产聚合物的关键方法.
- 了解影响ROP热力学因素对于设计新型聚合物至关重要.
研究的目的:
- 开发一种合成途径,以获得N替代的-2-.
- 为了研究这些morpholin-2-ones的有机催化环开放聚合.
- 为了探索形态素-2-one的结构及其聚合行为之间的关系.
主要方法:
- 使用催化剂氧化N替代的乙醇胺的乳化.
- 有机催化环开放聚合N-乙形态-2-的聚合.
- 实验和理论研究分析聚合热力学和原子金字塔化.
主要成果:
- 通过催化氧化乳化合成N替代的-2-.
- N-乙烯型甲-2-容易经历环开放聚合,形成多氨基.
- 聚合是对原子的杂交敏感的,N-或N-衍生物没有显示聚合.
- 通过去除聚N-Boc-morpholin-2-one的保护,可以获得水溶性,阴离子型的多形态.
结论:
- 这项研究提出了一种新的合成N替代形态素-2-及其随后的聚合.
- 内循环原子的杂交是指环开放聚合物的热力学的一个关键因素.
- 这项工作为制造功能化的聚氨和阴离子聚合物开辟了道路.
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