超分子化学
聚合物
高分子
超分子聚合物
共价键
材料科学
拓扑(电路)
纳米技术
网络拓扑
网络共价键合
聚合物网络
分子
高分子科学
计算机科学
化学
有机化学
复合材料
生物化学
数学
组合数学
操作系统
作者
Yuchen Guo,Yuhang Liu,Xinyang Zhao,Jun Zhao,Yongming Wang,Xinhai Zhang,Zhewen Guo,Xuzhou Yan
标识
DOI:10.1021/acsami.2c10404
摘要
Network topologies, especially some high-order topologies, are able to furnish cross-linked polymer materials with enhanced properties without altering their chemical composition. However, the fabrication of such topologically intriguing architectures at the macromolecular level and in-depth insights into their structure-property relationship remain a significant challenge. Herein, we relied on synergistic covalent-and-supramolecular polymers (CSPs) as a platform to prepare a range of polymer networks with an interwoven topology. Specifically, through the sequential supramolecular self-assemblies, the covalent polymers (CPs) and metallosupramolecular polymers (MSPs) could be interwoven in our CSPs by [2]pseudorotaxane cross-links. As a result, the obtained CSPs possessed a topological network that could not only promote the synergistic effect between CPs and MSPs to afford mechanically robust yet dynamic materials but also vest polymers with some functions, as manifested by force-induced hierarchical dissociations of supramolecular interactions and superior thermomechanical stability compared to our previously reported CSP systems. Furthermore, our CSPs exhibited tunable mechanical performance toward multiple stimuli including K+ and PPh3, demonstrating abundant stimuli-responsive properties. We hope that these findings could provide novel opportunities toward achieving topological structures at the macromolecular level and also motivate further explorations of polymeric materials via the way of controlling their topological structures.
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