Synthesis of poly(vinyl acetate) and poly(vinyl alcohol) containing block copolymers by combination of cobalt-mediated radical polymerization and ATRP

被引:90
作者
Debuigne, A
Caille, JR
Willet, N
Jérôme, R
机构
[1] Univ Liege, Ctr Educ & Res Macromol, B-4000 Liege, Belgium
[2] Solvay Res & Technol, B-1120 Brussels, Belgium
关键词
D O I
10.1021/ma051246x
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(vinyl acetate) (PVAc) chains of a low polydispersity (M-w/M-n similar to 1.1-1.2) have been prepared by cobalt-mediated radical polymerization of vinyl acetate (VAc). They have been end-capped by an activated bromide by addition of an alpha-bromoester or an alpha-bromoketone containing nitroxide and converted into effective macroinitiators for the atom transfer radical polymerization of styrene (Sty), ethyl acrylate, and methyl methacrylate. Because each block is formed by a controlled process, well-defined PVAc containing diblock copolymers are easily prepared. The PVAc-b-PS copolymers synthesized from alpha-bromoketone end-capped PVAc can be converted into well-defined poly(vinyl alcohol)-b-polystyrene amphiphiles by methanolysis of the poly(vinyl acetate) block. Self-association of an amphiphilic poly(vinyl alcohol)(3500)-b-polystyrene(16 600) in a (4/1) water/tetrahydrofuran mixture results in the formation of vesicles as observed by transmission electron microscopy.
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收藏
页码:9488 / 9496
页数:9
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