Non-covalent synthesis of supermicelles with complex architectures using spatially confined hydrogen-bonding interactions

被引:94
|
作者
Li, Xiaoyu [1 ]
Gao, Yang [1 ]
Boott, Charlotte E. [1 ]
Winnik, Mitchell A. [2 ]
Manners, Ian [1 ]
机构
[1] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
[2] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
基金
加拿大自然科学与工程研究理事会; 英国工程与自然科学研究理事会;
关键词
BLOCK-COPOLYMER MICELLES; CYLINDRICAL MICELLES; BUILDING-BLOCKS; JANUS PARTICLES; CO-MICELLES; LENGTH; POLYMERS; DNA; NANOSTRUCTURES; MORPHOLOGIES;
D O I
10.1038/ncomms9127
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nature uses orthogonal interactions over different length scales to construct structures with hierarchical levels of order and provides an important source of inspiration for the creation of synthetic functional materials. Here, we report the programmed assembly of monodisperse cylindrical block comicelle building blocks with crystalline cores to create supermicelles using spatially confined hydrogen-bonding interactions. We also demonstrate that it is possible to further program the self-assembly of these synthetic building blocks into structures of increased complexity by combining hydrogen-bonding interactions with segment solvophobicity. The overall approach offers an efficient, non-covalent synthesis method for the solution-phase fabrication of a range of complex and potentially functional supermicelle architectures in which the crystallization, hydrogen-bonding and solvophobic interactions are combined in an orthogonal manner.
引用
收藏
页数:8
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