弹性体
聚氨酯
氢键
对偶(语法数字)
债券
高分子化学
高分子科学
网络结构
材料科学
化学
复合材料
计算机科学
有机化学
业务
分子
哲学
语言学
财务
机器学习
作者
Aofei Zhang,Xiaoyu Du,Jianglong Li,Jianlong Wen,Lang Shuai,Yongqiang Ming,Yijing Nie
出处
期刊:Macromolecules
[American Chemical Society]
日期:2025-07-18
卷期号:58 (15): 8032-8043
被引量:12
标识
DOI:10.1021/acs.macromol.5c00565
摘要
How to effectively improve the strength and toughness of polymer elastomers is important for the expansion of their application fields. Construction of two distinct types of dynamic reversible bonds within elastomers represents an effective strategy for enhancing their mechanical properties. However, the interplay mechanisms between different dynamic reversible bonds have not been fully studied. Herein, we constructed both a hydrogen bond network and a metal coordination network in polyurethane (PU) elastomers. The introduction of both weak hydrogen bonds and strong metal coordination bonds can endow the elastomers with high tensile strength without the sacrifice of stretchability. This special phenomenon can be attributed to the dynamic synergistic mechanisms between the hydrogen bond network and coordination bond network. In short, the presence of strong coordination bonds can promote the orientation of local segments, while the recombination of weak hydrogen bonds can cause the relaxation of locally oriented segments.
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