
Thermo‐responsive topological metamorphosis in covalent‐and‐supramolecular polymer architectures
Author(s) -
Wang Yongming,
Zhang Hao,
Zhang Zhaoming,
Zhao Jun,
Bai Ruixue,
Liu Yuhang,
Zhang Xinhai,
Yan Xuzhou
Publication year - 2022
Publication title -
aggregate
Language(s) - English
Resource type - Journals
ISSN - 2692-4560
DOI - 10.1002/agt2.206
Subject(s) - supramolecular chemistry , supramolecular polymers , polymer , covalent bond , materials science , macromolecule , nanotechnology , self healing hydrogels , maleimide , topology (electrical circuits) , chemistry , polymer chemistry , molecule , organic chemistry , composite material , biochemistry , mathematics , combinatorics
Topological metamorphosis represents a powerful approach to modulate the properties of polymers. However, it still remains a major challenge to achieve the tunability of bulk mechanical properties via topological transformation in supramolecular polymer systems. Herein, we couple the covalent polymer and supramolecular polymer in a single system—referred to as covalent‐and‐supramolecular polymer (CSP)—to realize a thermo‐responsive macromolecular metamorphosis. The CSP is able to topologically switch from grafted polymer to cross‐linked network by taking advantage of synergistic dynamic covalent interactions and host–guest interactions. Benefiting from the topologically structural transformation, brittleness intrinsically evolves into toughness in our CSP architectures with minimum change of their molecular compositions from furan–maleimide to anthracene–maleimide linkers. Our work demonstrates that supramolecular polymers are a promising platform to design smart materials not only due to their inherent stimuli‐responsive properties but also because of their abilities in determining bulk mechanical properties of polymers with alterable topological structures.