An Orthogonal Dynamic Covalent Polymer Network with Distinctive Topology Transformations for Shape- and Molecular Architecture Reconfiguration

被引:28
|
作者
Miao, Wusha [1 ]
Yang, Bo [1 ]
Jin, Binjie [1 ]
Ni, Chujun [1 ]
Feng, Haijun [1 ]
Xue, Yaoting [3 ]
Zheng, Ning [1 ]
Zhao, Qian [1 ,2 ]
Shen, Youqing [1 ]
Xie, Tao [1 ,2 ]
机构
[1] Zhejiang Univ, Coll Chem & Biol Engn, State Key Lab Chem Engn, Hangzhou 310027, Peoples R China
[2] ZJU Hangzhou Global Sci & Technol Innovat Ctr, Hangzhou 311215, Peoples R China
[3] Zhejiang Univ, Dept Engn Mech, Inst Appl Mech, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Bottlebrush Polymer; Orthogonal Dynamic Covalent Bonds; Topological Transformation; SOLVENT-FREE; ELASTOMERS; SUPERSOFT; BEHAVIOR; DENSITY;
D O I
10.1002/anie.202109941
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bond exchange in a typical dynamic covalent polymer network allows access to macroscopic shape reconfigurability, but the network architecture is not altered. An alternative possibility is that the network architecture can be designed to switch to various topological states corresponding to different material properties. Achieving both in one network can expand the material scope, but their intrinsically conflicting mechanisms make it challenging. We design a dynamic covalent network that can undergo two orthogonal topological transformations, namely transesterification on the branched chains and olefin metathesis on the mainframe. This allows independent control of the macroscopic shape and molecular architecture. With this design, we illustrate a bottlebrush network with programmable shape and spatially definable mechanical properties. Our strategy paves a way to on-demand regulation of network polymers.
引用
收藏
页数:6
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