Thermoresponsive self-healable and recyclable polymer networks based on a dynamic quinone methide-thiol chemistry

被引:15
作者
Xiang, Lue [1 ,2 ]
Liu, Xianfeng [1 ,2 ]
Zhang, Huan [1 ]
Zhao, Ning [1 ,2 ]
Zhang, Ke [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Lab Polymer Phys & Chem, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
美国国家科学基金会;
关键词
TEMPERATURE; EXCHANGE; STIFF; BOND; TRANSESTERIFICATION; POLYURETHANE; VITRIMERS; DESIGN; ACCESS; AIR;
D O I
10.1039/d0py01008a
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A novel thermoresponsive dynamic covalent chemistry was developed based on 1,6-conjugate addition between a stablepara-quinone methide, namely 2,6-di-t-butyl-7-phenyl-p-quinone methide (pQM), and thiol nucleophiles. When applying it in the formation of polymer networks, covalently cross-linked polymer bulk materials were developed with thermoresponsive dynamic properties. This new type of dynamic covalent polymer network possesses wonderful structure stability at room temperature but demonstrates excellent self-healable and recyclable properties at high temperatures above 100 degrees C. The new thermoresponsivepQM-thiol dynamic covalent chemistry expanded the scope of dynamic covalent polymer network materials.
引用
收藏
页码:6157 / 6162
页数:6
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