Synthesis of nitroxide-containing block copolymers for the formation of organic cathodes

被引:54
|
作者
Hauffman, Guillaume [1 ]
Rolland, Julien [1 ]
Bourgeois, Jean-Pierre [1 ]
Vlad, Alexandru [2 ]
Gohy, Jean-Francois [1 ]
机构
[1] Catholic Univ Louvain, Inst Condensed Matter & Nanosci IMCN, Bio & Soft Matter BSMA, B-1348 Louvain, Belgium
[2] Catholic Univ Louvain, ICTEAM, B-1348 Louvain, Belgium
关键词
atom transfer radical polymerization (ATRP); block copolymers; copolymerization; electrochemistry; functionalization of polymers; organic radical battery; redox polymers; secondary amine; TEMPO polymer; TRANSFER RADICAL POLYMERIZATION; ELECTRODE; POLYMERS; BATTERY; PTMA; COMPOSITE; BRUSHES; CARBON; ATRP;
D O I
10.1002/pola.26279
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This contribution describes the polymerization of 2,2,6,6-tetramethylpiperidin-4-yl methacrylate by atom transfer radical polymerization (ATRP). Different catalytic systems are compared. The CuCl/4,4'-dinonyl-2,2'-dipyridyl catalytic system allows a good control over the polymerization and provides polymers with a polydispersity index below 1.2. The successful polymerization of styrene from PTMPM-Cl macroinitiators by ATRP is then demonstrated. Successful quantitative oxidation of PTMPM-b-PS block copolymers leads to poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl-methacrylate)-b-poly(styrene) (PTMA-b-PS). The cyclic voltammogram of PTMA-b-PS indicates a reversible redox reaction at 3.6 V (vs. Li+/Li). Such block copolymers open new opportunities for the formation of functional organic cathode materials. (C) 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013
引用
收藏
页码:101 / 108
页数:8
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