Synthesis and self-assembly of helical polypeptide-random coil amphiphilic diblock copolymer

被引:63
|
作者
Kuo, Shiao-Wei [1 ]
Lee, Hsin-Fang [2 ]
Huang, Chih-Feng [2 ]
Huang, Cheng-Jynn [2 ]
Chang, Feng-Chih [2 ]
机构
[1] Natl Sun Yat Sen Univ, Ctr Nanosci & Nanotechnol, Dept Mat Sci & Optoelect Engn, Kaohsiung 80424, Taiwan
[2] Natl Chiao Tung Univ, Inst Appl Chem, Hsinchu 30050, Taiwan
关键词
block copolymer; hydrogen bonding; polypeptide; self-assembly; self-organization;
D O I
10.1002/pola.22632
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Three amphiphilic rod-coil diblock copolymers, poly(2-ethyl-2-oxazoline-b-/-benzyl-L-glutamate) (PEOz-b-PBLG),G), incorporating the same-length PEOz block length and various lengths of their PBLG blocks, were synthesized through a combining of living cationic and N-carboxyanhydride (NCA) ring-opening polymerizations. In the bulk, these block copolymers display thermotropic liquid crystalline behavior. The self-assembled aggregates that formed from these diblock copolymers in aqueous solution exhibited morphologies that differed from those obtained in alpha-helicogenic solvents, that is, solvents in which the PBLG blocks adopt rigid alpha-helix conformations. In aqueous solution, the block copolymers self-assembled into spherical micelles and vesicular aggregates because of their amphiphilic structures. In helicogenic solvents (in this case, toluene and benzyl alcohol), the PEOz-b-PBLG copolymers exhibited rod-coil chain properties, which result in a diverse array of aggregate morphologies (spheres, vesicles, ribbons, and tube nanostructures) and thermoreversible gelation behavior. (C) 2008 Wiley Periodicals, Inc.
引用
收藏
页码:3108 / 3119
页数:12
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