Overview of cobalt-mediated radical polymerization: Roots, state of the art and future prospects

被引:314
作者
Debuigne, Antoine [1 ]
Poli, Rinaldo [2 ,3 ,4 ]
Jerome, Christine [1 ]
Jerome, Robert [1 ]
Detrembleur, Christophe [1 ]
机构
[1] Univ Liege, Ctr Educ & Res Macromol, B-4000 Liege, Belgium
[2] Univ Toulouse 3, Chim Coordinat Lab, CNRS, UPR Liee Convent 8241, F-31077 Toulouse, France
[3] Inst Natl Polytech Toulouse, F-31077 Toulouse, France
[4] Inst Univ France, F-75005 Paris, France
关键词
Controlled radical polymerization; Cobalt-mediated radical polymerization; Copolymers; Macromolecular engineering; CO-C BOND; ORGANOCOBALT PORPHYRIN COMPLEXES; FRAGMENTATION CHAIN TRANSFER; VINYL-ACETATE; DISSOCIATION ENERGIES; DEGENERATIVE TRANSFER; METHYL-METHACRYLATE; POLY(VINYL ACETATE); ORGANIC-SYNTHESIS; BLOCK-COPOLYMERS;
D O I
10.1016/j.progpolymsci.2008.11.003
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Controlled radical polymerization (CRP) techniques offer the opportunity to properly design polymer chains and adjust their chemical and physical properties. Among these techniques, cobalt-mediated radical polymerization (CMRP) distinguished itself by the high level of control imparted to the polymerization of acrylic and vinyl ester monomers, even for high molar masses. This article summarizes for the first time the advances in understanding and synthetic scope of CMRP since its discovery. Notably, the cobalt-carbon bond formation by dual contribution of reversible termination and degenerative chain transfer is discussed, as well as the impact of additives able to coordinate the metal. The potential of computational chemistry in the field of CMRP as a rationalization and predicting tool is also presented. These mechanistic considerations and achievements in macromolecular engineering will be discussed along with challenges and future prospects in order to assess the CMRP system as a whole. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:211 / 239
页数:29
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