Self-Assembly of Multiblock Copolymers

被引:34
|
作者
Qiang, Xiaolian [1 ,2 ]
Chakroun, Ramzi [1 ,2 ]
Janoszka, Nicole [1 ,2 ]
Groeschel, Andre H. [1 ,2 ]
机构
[1] Univ Duisburg Essen, Phys Chem, D-47057 Duisburg, Germany
[2] Univ Duisburg Essen, Ctr Nanointegrat CENIDE, D-47057 Duisburg, Germany
关键词
Block copolymers; colloids; morphologies; Janus nanoparticles; nanostructures; self-assembly; ABC TRIBLOCK COPOLYMERS; BLOCK-COPOLYMERS; JANUS PARTICLES; MULTICOMPARTMENT MICELLES; DIBLOCK COPOLYMERS; VERSATILE APPROACH; FACILE SYNTHESIS; POLYMER BLENDS; PHASE-BEHAVIOR; SHAPE;
D O I
10.1002/ijch.201900044
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Block copolymers (BCPs) are a subclass of soft matter extensively used in materials science and nanomedicine. They consist of two or more incompatible segments and are prone to self-assemble into nanostructures with a characteristic size of 10-100 nm. BCPs thus naturally address the structural dimension between molecular and colloidal scales. This review gives a brief overview of recent developments in BCP self-assembly under various conditions. Special emphasis is put on linear BCPs with three or more sequentially linked blocks, i. e. ABC triblock terpolymers, ABAC tetrablock terpolymers, and so on. We discuss their microphase separation in bulk, in the confinement of nanoemulsion droplets, and their hierarchical self-assembly to multicompartment nanostructures in selective solvents. Regarding applications, block copolymers are widely used in templating and drug delivery, but their inherent asymmetry is also particularly useful for the synthesis of Janus nanoparticles.
引用
收藏
页码:945 / 958
页数:14
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