Regulating the Dynamic Properties of Knoevenagel Condensation Cross-Linked Hydrogels via Thia-Michael Addition Reaction.

IF 4.1 3区 化学 Q2 POLYMER SCIENCE
Yu Yan, Ruizhu Yang, Mingming Zhao, Yuqian Ji, Zhiqiang Sun, Xiaonong Zhang, Chunsheng Xiao
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引用次数: 0

Abstract

The strategies for regulating dynamic mechanical properties of dynamic hydrogels have attracted significant attention. Herein, we developed a new strategy to regulate the dynamic properties of Knoevenagel condensation (KC) reaction cross-linked hydrogels through reversible thia-Michael addition reaction. In this system, the dynamic C═C bonds formed by the reversible KC reaction could react with thiols via the reversible Michael addition reaction, leading to the structural changes from C═C to C─C bonds and thereby enabling effective modulation of the hydrogel's viscoelastic behaviors. Furthermore, decreasing the pH reduced the reverse reaction rates of both the KC reaction and the thia-Michael addition reaction, reinforcing the stability of the C═C bonds and thia-Michael adducts. To implement this dual regulation, N-acetylcysteine, a small molecule containing both thiol and carboxyl groups, was introduced, which allowed synergistic modulation through thiol-C═C reversible addition and pH responsiveness. This cooperative regulation enables fine-tuned control of hydrogel dynamics, extending stress relaxation time from 20 to 1900 s, enhancing the storage modulus from 2205 to 4705 Pa, and improving the structural stability. Overall, this reversible thia-Michael addition-mediated mechanism paves a new way for regulating the dynamic properties of the KC reaction cross-linked hydrogels.

通过Thia-Michael加成反应调节Knoevenagel缩合交联水凝胶的动力学性质。
动态水凝胶动态力学性能的调控策略引起了人们的广泛关注。本文提出了一种新的策略,通过可逆的thia-Michael加成反应来调节Knoevenagel缩合反应交联水凝胶的动力学性质。在该体系中,由可逆KC反应形成的动态C = C键可以通过可逆Michael加成反应与硫醇反应,导致从C = C到C─C键的结构变化,从而能够有效地调节水凝胶的粘弹性行为。此外,降低pH降低了KC反应和thia-Michael加成反应的逆反应速率,增强了C = C键和thia-Michael加合物的稳定性。为了实现这种双重调节,引入了n -乙酰半胱氨酸,一种同时含有巯基和羧基的小分子,它允许通过巯基C = C可逆加成和pH响应性进行协同调节。这种协同调节可以实现水凝胶动力学的微调控制,将应力松弛时间从20 s延长到1900 s,将存储模量从2205提高到4705 Pa,并提高结构稳定性。总的来说,这种可逆的thia-Michael加成介导机制为调节KC反应交联水凝胶的动力学性质开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Macromolecular Rapid Communications
Macromolecular Rapid Communications 工程技术-高分子科学
CiteScore
7.70
自引率
6.50%
发文量
477
审稿时长
1.4 months
期刊介绍: Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.
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