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具有交织拓扑结构的协同共价和超分子聚合物。

Synergistic Covalent-and-Supramolecular Polymers with an Interwoven Topology.

机构信息

School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory of Electrical Insulation and Thermal Aging, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2023 May 31;15(21):25161-25172. doi: 10.1021/acsami.2c10404. Epub 2022 Jul 27.

Abstract

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 PPh, 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.

摘要

网络拓扑结构,尤其是一些高阶拓扑结构,可以在不改变其化学成分的情况下,为交联聚合物材料提供增强的性能。然而,在高分子水平上制造这种拓扑结构引人入胜的结构,并深入了解其结构-性能关系仍然是一个重大挑战。在这里,我们依赖协同共价和超分子聚合物(CSP)作为平台,制备了一系列具有交织拓扑结构的聚合物网络。具体来说,通过顺序的超分子自组装,共价聚合物(CPs)和金属超分子聚合物(MSPs)可以通过[2]伪轮烷交联在我们的 CSP 中交织。结果,所得到的 CSP 具有拓扑网络,不仅可以促进 CPs 和 MSPs 之间的协同效应,从而提供机械坚固但动态的材料,而且还可以赋予聚合物一些功能,如表现出超分子相互作用的力诱导分级解离和优于我们之前报道的 CSP 系统的热机械稳定性。此外,我们的 CSP 对包括 K 和 PPh 在内的多种刺激表现出可调的机械性能,表现出丰富的刺激响应特性。我们希望这些发现可以为在高分子水平上实现拓扑结构提供新的机会,并激励通过控制拓扑结构来进一步探索聚合物材料。

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