高等学校化学学报 ›› 2001, Vol. 22 ›› Issue (S1): 232.

• 研究论文 • 上一篇    下一篇

原子转移自由基活性聚合合成PS-PMA-PS嵌段聚合物

高立超1,2, 史林启1, 张望清1, 高俊刚2, 何炳林1   

  1. 1. 南开大学吸附分离功能高分子材料国家重点实验室, 南开大学高分子化学研究所, 天津 300071;
    2. 河北大学化学与环境科学学院, 保定 071002
  • 收稿日期:2001-07-17 出版日期:2001-12-31 发布日期:2001-12-31
  • 通讯作者: 史林启(1963年出生),男,博士,教授,博士生导师.从事高分子纳米结构功能材料和生物医用高分子的研究.
  • 基金资助:

    国家自然科学基金(批准号:59873012)和教育部高等学校骨干教师资助计划项目资助.

Controlled Sequential Polymerization of PS-PMA-PS by ATRP

GAO Li-Chao1,2, SHI Lin-Qi1, ZHANG Wang-Qing1, GAO Jun-Gang2, HE Bing-Lin1   

  1. 1. State Key Laboratory of Functional Polymer Materials for Adsorption and Separation Institute of Polymer Chemistry, Nankai University, Tianjin 300071;
    2. Department of Chemistry, Hebei University, Baoding 071002, China
  • Received:2001-07-17 Online:2001-12-31 Published:2001-12-31

摘要:

本文采用氯化亚铜/α,α'-联吡啶配位化合物作催化剂.首先在130℃时用1-苯基氯乙烷在引发苯乙烯(St)进行原子转移自由基聚合,再以其产物PS-Cl作为大分子引发剂引发丙烯酸甲酯(MA)在反应温度为120℃时进行聚合,得到两嵌段聚合物PS-PMA-Cl.此两嵌段共聚物在特殊混合溶剂——丙酮/正丙醇(体积比7:3)中仍然可以作大分子引发剂引发苯乙烯进行原子转移自由基聚合,由于聚合体系接近于均相.所以表现出了较高的反应活性,并且合成的聚苯乙烯一聚丙烯酸甲酯一聚苯乙烯(PS-PMA-PS)三嵌段聚合物的分子量与设计值接近、分子量分布比较窄,反应的条件温和,可控性好.最后通过NMR技术对三元嵌段共聚物的结构迸行了表征.

关键词: 原子转移自由基聚合, 三嵌段聚合物, 水解

Abstract:

Polystrene-Polymethyl acrylate-Polystyrene tri-block copolymer (PS-PMA-PS) was synthesized by modified atom transfer radical polymerization. Using CuCl/α,α'-Bipyridyl complex as catalyst, initiated by 1-PECl,styrene was first polymerized at 130℃. Then using the product as macroinitiator, the di-block (PS-PMA) copolymer were obtained. Meanwhile the tri-block copolymer has also been prepared after adding styrene and actone/l-propanol into the reaction system. PS-PMA-PS was characterized by 1H-NMR and GPC techniques. The results show that the molecular weight distribution of the tri-block copolymer is narrow (MwMn=1.19) as the conversion of monomer is around 70-85%. The molecular weight of the block is in good agreement with designed value. The NMR testified the structure of PS-PAA-PS which was obtained by hydrolyzing PS-PMA-PS.

Key words: Atom transfer radical polymerization, tri-block copolymer, hydrolysis

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