Synthesis and Postfunctionalization of Well-Defined Star Polymers via "Double" Click Chemistry

被引:23
作者
Boyer, Cyrille [1 ]
Whittaker, Michael [1 ]
Davis, Thomas P. [1 ]
机构
[1] Univ New S Wales, Sch Chem Engn, CAMD, Sydney, NSW 2052, Australia
基金
澳大利亚研究理事会;
关键词
activated ester; click chemistry; functionalization of polymers; radical polymerization; reversible addition fragmentation chain transfer polymerization (RAFT); star polymer; thiol-ene; TRANSFER RADICAL POLYMERIZATION; RAFT POLYMERIZATION; POLY(ETHYLENE OXIDE); FUNCTIONAL POLYMERS; DRUG-DELIVERY; CORE; WATER; RHEOLOGY; DESIGN; ATRP;
D O I
10.1002/pola.25001
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this article, the synthesis and the functionalization of well-defined, narrow polydispersity (polydispersity index < 1.2) star polymers via reversible addition-fragmentation chain transfer polymerization is detailed. In this arm first approach, the initial synthesis of a poly(pentafluorophenyl acrylate) polymer, and subsequent, cross-linking using bis-acrylamide to prepare star polymers, has been achieved by reversible addition fragmentation chain transfer polymerization. These star polymers were functionalized using a variety of amino functional groups via nucleophilic substitution of pentafluorophenyl activated ester to yield star polymers with predesigned chemical functionality. This approach has allowed the synthesis of star glycopolymer using a very simple approach. Finally, the core of the stars was modified via thiolene click chemistry reaction using fluorescein-o-acrylate and DyLigh 633 Maleimide. (C) 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 49: 5245-5256, 2011
引用
收藏
页码:5245 / 5256
页数:12
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