Clickable amphiphilic triblock copolymers

被引:24
|
作者
Isaacman, Michael J. [1 ,2 ]
Barron, Kathryn A. [1 ]
Theogarajan, Luke S. [1 ,3 ]
机构
[1] Univ Calif Santa Barbara, Calif NanoSyst Inst UC Santa Barbara, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Elect & Comp Engn, Santa Barbara, CA 93106 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
click chemistry; self-assembly; triblock copolymers; POLYMERS; POLY(2-OXAZOLINE)S; CHEMISTRY; DRUG; POLYSILOXANE; COMPLEXES; BLOCK;
D O I
10.1002/pola.25989
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Amphiphilic polymers have recently garnered much attention due to their potential use in drug delivery and other biomedical applications. A modular synthesis of these polymers is extremely desirable, because it offers precise individual block characterization and increased yields. We present here for the first time a modular synthesis of poly(oxazoline)poly(siloxane)poly(oxazoline) block copolymers that have been clicked together using the copper-catalyzed azidealkyne cycloaddition reaction. Various click methodologies for the synthesis of these polymers have been carefully evaluated and optimized. The approach using copper nanoparticles was found to be the most optimal among the methods evaluated. Furthermore, these results were extended to allow for a reactive Si?H group-based siloxane middle block to be successfully clicked. This enables the design of more complex amphiphilic block copolymers that have additional functionality, such as stimuli responsiveness, to be synthesized via a simple hydrosilylation reaction. (c) 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012
引用
收藏
页码:2319 / 2329
页数:11
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