吉林大学学报(理学版)

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eROP结合ROMP合成嵌段聚合物PCL-b-PB-b-PCL

姜伟1, 安妮1, 刘葵2, 相世栋1, 汤钧1   

  1. 1. 吉林大学 化学学院, 长春 130012; 2. 辽宁大学出版社, 沈阳 110036
  • 收稿日期:2015-01-21 出版日期:2015-11-26 发布日期:2015-11-23
  • 通讯作者: 汤钧 E-mail:chemjtang@jlu.edu.cn

Synthesis of Block Polymers PCL-b-PB-b-PCL by Tandem eROP and ROMP

JIANG Wei1, AN Ni1, LIU Kui2, XIANG Shidong1, TANG Jun1   

  1. 1. College of Chemistry, Jilin University, Changchun 130012, China;2. Liaoning University Press, Shenyang 110036, China
  • Received:2015-01-21 Online:2015-11-26 Published:2015-11-23
  • Contact: TANG Jun E-mail:chemjtang@jlu.edu.cn

摘要:

采用新型化学酶法--开环易位聚合反应(ROMP)与酶促开环聚合反应(eROP)联用合成嵌段聚合物PCL-b-PB-b-PCL, 用核磁共振氢谱
( 1H NMR)、 凝胶渗透色谱(GPC)和差示扫描量热法(DSC)表征产物的结构并进行性能测试. 结果表明: GPC数据向高分子量移动, 即成功合成了嵌段聚合物; 嵌段聚合物可完全水解, 且GPC数据向低分子量移动, 表明该方法可行、 有效.

关键词: 开环易位聚合反应, 酶促开环聚合反应, 化学酶法, 嵌段聚合物

Abstract:

Copolymer PCL\|b\|PB\|b\|PCL was successfully prepared by a novel chemoenzymatic strategy coupled with  enzymatic ringopening polymerization
 (eROP)  and ringopening metathesis polymerization (ROMP). The chemical structures of the products were characterized by 1H NMR, GPC and DSC. A complete shift of the GPC trace to higher molecular weights  illustrates that the copolymer was successfully prepared.  1H NMR data clearly show  block in the copolymer is hydrolyzed completely, and a clear shift of the GPC trace to lower molecular weights  illustrates that the synthetic strategy is reliability.

Key words: ring-opening metathesis polymerization (ROMP), enzymatic ring-opening polymerization(eROP), chemoenzymatic, block polymer

中图分类号: 

  • O641.2