Mechanically linked supramolecular polymer architectures derived from macromolecular [2]rotaxanes: Synthesis and topology transformation

被引:29
作者
Aoki, Daisuke [1 ]
Takata, Toshikazu [1 ,2 ]
机构
[1] Tokyo Inst Technol, Dept Chem Sci & Engn, Meguro Ku, Tokyo 1528552, Japan
[2] JST CREST, Meguro Ku, Tokyo 1528552, Japan
关键词
MOVABLE CROSS-LINKER; SLIDE-RING GELS; POLYROTAXANE NETWORK; BLOCK-COPOLYMERS; CROWN-ETHERS; RADICAL POLYMERIZATION; MACROCYCLIC POLYMERS; TEMPLATED SYNTHESIS; SIZE-COMPLEMENTARY; ROTAXANE SYNTHESIS;
D O I
10.1016/j.polymer.2017.08.020
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This review article deals with the construction and function of dynamic macromolecular systems having mechanically linked polymer chains which can undertake a topology transformation to induce structure and property changes. Synthesis of a macromolecular [2] rotaxane (M2R) possessing a macromolecular switch function is first described, which is a structure-definite ideal polyrotaxane consisting of one polymer axle and one macrocycle wheel. Its application to the synthesis of rotaxane cross-linked polymers (RCP) and topology-transformable polymers is discussed along with their properties, where the rotaxane-linking of polymer chains plays a crucial role. The M2R-based cross-linker is prepared and applied to the synthesis of RCPs by adding it into radical polymerization systems of vinyl monomers. RCPs have high stretchability and toughness. Rotaxane-linked block copolymers and cyclic polymers synthesized by introducing polymer chains onto the wheel and axle components of M2R are subjected to the topology transformation using the switch function of M2R to cause remarkable structure and property changes. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:276 / 296
页数:21
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