共聚物
高分子化学
胶束
乙二醇
两亲性
原子转移自由基聚合
材料科学
甲基丙烯酸酯
木筏
链式转移
自由基聚合
化学
有机化学
聚合物
水溶液
复合材料
作者
Tian‐Lu Cheng,Hao‐Jie Zhu,E. T. Kang,K. G. Neoh
出处
期刊:Langmuir
[American Chemical Society]
日期:2005-07-09
卷期号:21 (16): 7180-7185
被引量:84
摘要
Two brush-type amphiphilic diblock copolymers, poly(poly(ethylene glycol)methyl ether methacrylate-block-polystyrene) (P(PEGMA)-b-PS) and poly(glycidyl methacrylate)-block-poly(poly(ethylene glycol)methyl ether methacrylate) (P(GMA)-b-P(PEGMA)) were synthesized, respectively, via consecutive atom-transfer radical polymerizations (ATRPs) and reversible addition-fragmentation chain-transfer (RAFT) polymerizations. The diblock copolymers were characterized by gel permeation chromatography (GPC), (1)H nuclear magnetic resonance (NMR) spectroscopy, and FT-IR spectroscopy. The aggregation behavior of the two amphiphilic diblock copolymers in water was also studied. Scanning electron and transmission electron microscopic images revealed that spherical micelles (40-80 nm in diameter) from self-assembly of the P(PEGMA)-b-PS copolymers and wormlike micelles (60-120 nm in length and 20-30 nm in diameter) from self-assembly of the P(GMA)-b-P(PEGMA) copolymers were prevalent. The spherical P(PEGMA)-b-PS micelles could self-assemble gradually into giant aggregates of several micrometers in diameter.
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