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高丝氨酸内酯作为合成多功能聚合物的结构关键要素。

Homoserine Lactone as a Structural Key Element for the Synthesis of Multifunctional Polymers.

作者信息

Marquardt Fabian, Mommer Stefan, Lange Justin, Jeschenko Pascal M, Keul Helmut, Möller Martin

机构信息

Institute of Technical and Macromolecular Chemistry, RWTH Aachen University and DWI-Leibniz-Institute for Interactive Materials, Forckenbeckstr. 50, D-52056 Aachen, Germany.

出版信息

Polymers (Basel). 2017 Apr 5;9(4):130. doi: 10.3390/polym9040130.

Abstract

The use of bio-based building blocks for polymer synthesis represents a milestone on the way to "green" materials. In this work, two synthetic strategies for the preparation of multifunctional polymers are presented in which the key element is the functionality of homoserine lactone. First, the synthesis of a bis cyclic coupler based on a thiolactone and homoserine lactone is displayed. This coupler was evaluated regarding its regioselectivity upon reaction with amines and used in the preparation of multifunctional polymeric building blocks by reaction with diamines. Furthermore, a linear polyglycidol was functionalized with homoserine lactone. The resulting polyethers with lactone groups in the side chain were converted to cationic polymers by reaction with 3-(dimethylamino)-1-propylamine followed by quaternization with methyl iodide.

摘要

使用生物基构建块进行聚合物合成是迈向“绿色”材料道路上的一个里程碑。在这项工作中,提出了两种制备多功能聚合物的合成策略,其中关键要素是高丝氨酸内酯的官能团。首先,展示了基于硫内酯和高丝氨酸内酯的双环偶联剂的合成。对该偶联剂与胺反应时的区域选择性进行了评估,并用于通过与二胺反应制备多功能聚合物构建块。此外,用高丝氨酸内酯对线性聚缩水甘油进行官能化。所得侧链带有内酯基团的聚醚通过与3-(二甲基氨基)-1-丙胺反应,然后用碘甲烷季铵化,转化为阳离子聚合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/539b/6432242/e584eb4aaf59/polymers-09-00130-sch001.jpg

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