Transition metal catalysts for controlled radical polymerization

被引:516
作者
di Lena, Fabio [1 ,2 ]
Matyjaszewski, Krzysztof [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
[2] ASTAR, Inst Chem & Engn Sci, Jurong Isl 627833, Singapore
基金
瑞士国家科学基金会;
关键词
Metal catalysis; Controlled radical polymerization; Organometallic mediated radical polymerization; Atom transfer radical polymerization; Degenerative transfer radical polymerization; Reaction mechanism; ACTIVATION RATE CONSTANTS; RING-OPENING-METATHESIS; N-BUTYL METHACRYLATE; SCHIFF-BASE LIGANDS; CP2TICL-CATALYZED SET REDUCTION; RUTHENIUM-ALKYLIDENE CATALYSTS; ATOM-TRANSFER POLYMERIZATION; NEUTRAL PALLADIUM COMPLEXES; TRIDENTATE NITROGEN DONOR; POLYETHYLENE CHAIN GROWTH;
D O I
10.1016/j.progpolymsci.2010.05.001
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
The discovery, in the mid 1990s, that certain cobalt, ruthenium and copper complexes could effectively control the radical polymerization of a number of polar olefins, allowing for the facile synthesis of complex macromolecular architectures, fostered an intense search for increasingly better performing catalysts. As a consequence, several metal complexes were designed and tested. This article presents an organized and detailed overview of the most significant developments in the use of transition metal compounds to initiate, mediate and control radical polymerization, i.e., atom transfer radical polymerization or organometallic mediated radical polymerization. The catalysts have been classified according to the group of the periodic table to which the relative metal centers belong. Their catalytic performance, the mechanism with which they are supposed to operate, the structure-reactivity correlations as well as the type of monomers and experimental conditions employed are described. The use and the role of non-transition metal complexes in controlled radical polymerization are also discussed. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:959 / 1021
页数:63
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