Self-assembly of amphiphilic block pendant polymers as microphase separation materials and folded flower micelles

被引:34
|
作者
Matsumoto, Mayuko [1 ]
Takenaka, Mikihito [2 ,3 ]
Sawamoto, Mitsuo [1 ,4 ]
Terashima, Takaya [1 ]
机构
[1] Kyoto Univ, Dept Polymer Chem, Grad Sch Engn, Nishikyo Ku, Kyoto 6158510, Japan
[2] Kyoto Univ, Inst Chem Res, Uji, Kyoto 6110011, Japan
[3] RIKEN SPring 8 Ctr, Sayo, Hyogo 6795118, Japan
[4] Chubu Univ, Inst Sci & Technol Res, 1200 Matsumoto Cho, Kasugai, Aichi 4878501, Japan
基金
日本学术振兴会;
关键词
RANDOM COPOLYMERS; CRYSTALLIZATION;
D O I
10.1039/c9py01078e
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Herein, we created amphiphilic polymers bearing hydrophilic/hydrophobic block pendants as a new class of self-assembled materials for microphase separation in the solid state and forming folded flower micelles in water. For this, we designed amphiphilic block methacrylates comprising hydrophilic poly(ethylene glycol) (PEG) and a hydrophobic dodecyl group: DPEG10MA and DPEG23MA. The DPEG10MA and DPEG23MA homopolymers induced microphase separation of the block pendants. For example, the DPEG23MA homopolymer formed lamellar structures; the hydrophilic and crystallized PEG and hydrophobic dodecyl units are alternately layered with about 14 nm domain spacing. In water, random copolymers of PEG methyl ether methacrylate and DPEG10MA folded into flower micelles with both looped and linear PEG shells, where the dodecyl groups of the incorporated DPEG10MA assembled to form hydrophobic cores. The micelles further showed thermoresponsive solubility in water. The size, aggregation number, and cloud point of the micelles were controlled by their composition and chain length.
引用
收藏
页码:4954 / 4961
页数:8
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