Self-assembly of "patchy" nanoparticles: a versatile approach to functional hierarchical materials

被引:113
|
作者
Lunn, David J. [1 ]
Finnegan, John R. [1 ]
Manners, Ian [1 ]
机构
[1] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
基金
英国工程与自然科学研究理事会;
关键词
CRYSTALLINE-CORE MICELLES; BLOCK-COPOLYMER MICELLES; CYLINDRICAL MICELLES; SUPRAMOLECULAR POLYMERIZATION; COLLOIDAL POLYMERIZATION; ANIONIC-POLYMERIZATION; ARCHITECTURES; GROWTH; NANOSTRUCTURES; POLYMERS;
D O I
10.1039/c5sc01141h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The solution-phase self-assembly or "polymerization" of discrete colloidal building blocks, such as "patchy" nanoparticles and multicompartment micelles, is attracting growing attention with respect to the creation of complex hierarchical materials. This approach represents a versatile method with which to transfer functionality at the molecular level to the nano- and microscale, and is often accompanied by the emergence of new material properties. In this perspective we highlight selected recent examples of the self-assembly of anisotropic nanoparticles which exploit directional interactions introduced through their shape or surface chemistry to afford a variety of hierarchical materials. We focus in particular on the solution self-assembly of block copolymers as a means to prepare multicompartment or "patchy" micelles. Due to their potential for synthetic modification, these constructs represent highly tuneable building blocks for the fabrication of a wide variety of functional assemblies.
引用
收藏
页码:3663 / 3673
页数:11
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