Novel Self-Assembling Amino Acid-Derived Block Copolymer with Changeable Polymer Backbone Structure

被引:7
|
作者
Koga, Tomoyuki [1 ]
Aso, Eri [1 ]
Higashi, Nobuyuki [1 ]
机构
[1] Doshisha Univ, Fac Sci & Engn, Dept Mol Chem & Biochem, Kyoto 6100321, Japan
基金
日本学术振兴会;
关键词
DIBLOCK COPOLYMERS; SUPRAMOLECULAR MATERIALS; RADICAL POLYMERIZATION; ACYL MIGRATION; PEPTIDE; WATER; HYDROGELS; VESICLES; DESIGN; PH;
D O I
10.1021/acs.langmuir.6b01617
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Block copolymers have attracted much attention as potentially interesting building blocks for the development of novel nanostructured materials in recent years. Herein, we report a new type of self-assembling block copolymer with changeable polymer backbone structure, poly(Fmoc-Ser)(ester)-b-PSt, which was synthesized by combining the polycondensation of 9-fluorenylmethoxycarbonylserine (Fmoc-Ser) with the reversible addition-fragmentation chain transfer (RAFT) polymerization of styrene (St). This block copolymer showed the direct conversion of the backbone structure from polyester to polypeptide through a multi O,N-aryl migration triggered by base-induced deprotection of Fmoc groups in organic solvent. Such polymer-to-polymer conversion was found to occur quantitatively without decrease in degree of polymerization and to cause a drastic change in self-assembling property of the block copolymer. On the basis of several morphological analyses using FTIR spectroscopy, atomic force, and transmission and scanning electron microscopies, the resulting peptide block copolymer was found to self-assemble into a vesicle-like hollow nanosphere with relatively uniform diameter of ca. 300 nm in toluene. In this case, the peptide block generated from polyester formed beta-sheet structure, indicating the self-assembly via peptide-guided route. We believe the findings presented in this study offer a new concept for the development of self-assembling block copolymer system.
引用
收藏
页码:12378 / 12386
页数:9
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