Polyisobutylene-b-Poly(N,N-diethylacrylamide) Well-Defined Amphiphilic Diblock Copolymer: Synthesis and Thermo-Responsive Phase Behavior

被引:7
|
作者
Ren, Chunhong [1 ]
Liu, Xunwei [2 ]
Jiang, Xue [1 ]
Sun, Gang [2 ]
Huang, Xiaoyu [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Synthet & Self Assembly Chem Organ Funct, Shanghai 200032, Peoples R China
[2] Jinan Mil Gen Hosp, Dept Med Imaging, Jinan 250031, Peoples R China
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
block copolymer; poly(N; N-diethylacrylamide); RAFT; synthesis; thermo-responsive; TRANSFER RADICAL POLYMERIZATION; LIVING CARBOCATIONIC POLYMERIZATION; BLOCK-COPOLYMERS; RAFT POLYMERIZATION; TRIBLOCK COPOLYMERS; AQUEOUS-SOLUTIONS; MULTIPLE MORPHOLOGIES; ATRP; POLY(N; N-DIETHYLACRYLAMIDE); ACID);
D O I
10.1002/pola.27545
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polyisobutylene-b-poly(N,N-diethylacrylamide) (PIB-b-PDEAAm) well-defined amphiphilic diblock copolymers were synthesized by sequential living carbocationic polymerization and reversible addition-fragmentation chain transfer (RAFT) polymerization. The hydrophobic polyisobutylene segment was first built by living carbocationic polymerization of isobutylene at -70 degrees C followed by multistep transformations to give a well-defined (M-w/M-n=1.22) macromolecular chain transfer agent, PIB-CTA. The hydrophilic poly(N,N-diethylacrylamide) block was constructed by PIB-CTA mediated RAFT polymerization of N,N-diethylacrylamide at 60 degrees C to afford the desired well-defined PIB-b-PDEAAm diblock copolymers with narrow molecular weight distributions (M-w/M-n 1.26). Fluorescence spectroscopy, transmission electron microscope, and dynamic light scattering (DLS) were employed to investigate the self-assembly behavior of PIB-b-PDEAAm amphiphilic diblock copolymers in aqueous media. These diblock copolymers also exhibited thermo-responsive phase behavior, which was confirmed by UV-Vis and DLS measurements. (c) 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 1143-1150
引用
收藏
页码:1143 / 1150
页数:8
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