自愈水凝胶
大分子单体
超分子化学
材料科学
高分子化学
高分子科学
共聚物
化学
纳米技术
化学工程
有机化学
聚合物
复合材料
分子
工程类
作者
Lei Zou,Yingying Zhang,Yingying Zhang,Fangdong Ning,Xinxin Fu,Matthew J. Webber,Yongjun Zhang,Yongjun Zhang
出处
期刊:Macromolecules
[American Chemical Society]
日期:2025-06-23
卷期号:58 (13): 6935-6942
被引量:5
标识
DOI:10.1021/acs.macromol.5c01298
摘要
The macroscopic properties of polymer hydrogels are fundamentally governed by the network composition, structural topology, and cross-linking mechanisms. In this study, we prepared dynamic-covalent hydrogels from multiarm polyethylene glycol (PEG) analogs, using movable supramolecular cores to prepare 4-arm PEG mimics. This new architecture was achieved by using cucurbit[8]uril (CB[8]) host–guest complexes as functional cores for acylhydrazine-modified telechelic guests, followed by cross-linking with linear bis-aldehyde functionalized PEG chains via dynamic-covalent acylhydrazone bond formation. Rapid dynamics of the CB[8]–guest complexes comprising the movable core led to highly dynamic viscoelastic properties. Hydrogels with slow dynamic CB[8]–guest complexes as the movable core exhibited exceptional mechanical properties with deformation rate-dependent characteristics. This material showed extreme stretchability, elongating up to 70 times its original length before breaking. Comparative analysis with conventional hydrogels containing tetravalent macromonomers with static cores revealed that association–dissociation kinetics of the host–guest complexes play a key role in mediating the observed rate-dependent mechanical properties. This work offers the first successful design and fabrication of hydrogels prepared from 4-arm PEG analogs incorporating movable and dynamic CB[8] host–guest cores, thereby establishing a new paradigm in hydrogel engineering.
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