Functional polymers by atom transfer radical polymerization

被引:1175
作者
Coessens, V [1 ]
Pintauer, T [1 ]
Matyjaszewski, K [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
基金
美国安德鲁·梅隆基金会; 美国国家科学基金会;
关键词
functional polymers; atom transfer radical polymerization; review;
D O I
10.1016/S0079-6700(01)00003-X
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Atom transfer radical polymerization (ATRP) is one of the most successful methods to polymerize styrenes, (meth)acrylates and a variety of other monomers in a controlled fashion, yielding polymers with molecular weights predetermined by the ratio of the concentrations of consumed monomer to introduced initiator and with low polydispersities. Because of its radical nature, ATRP is tolerant to many functionalities in monomers leading to polymers with functionalities along the chains. Moreover, the initiator used determines the end groups of the polymers. By using a functional initiator, functionalities such as vinyl, hydroxyl, epoxide, cyano and other groups have been incorporated at one chain end, while the other chain end remains an alkyl halide. The polymer can be dehalogenated in a one-pot process or the halogen end groups can be transformed to other functionalities using nucleophilic substitution reactions or electrophilic addition reactions. Moreover, utilizing the ability of the halogen chain end to be reactivated, radical addition reactions can be used to incorporate allyl end groups, insert one less reactive monomer unit at the chain end, or to end-cap the polymer chain. With ATRP, functionality and architecture can be combined resulting in multifunctional polymers of different compositions and shapes such as block copolymers, multiarmed stars or hyperbranched polymers. (C) 2001 Elsevier Science Ltd. All rights reserved.
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页码:337 / 377
页数:41
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