Tough supramolecular hydrogels of poly(N,N-dimethylacrylamide)-grafted poly(methacrylic acid) with cooperative hydrogen bonds as physical crosslinks†

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL Soft Matter Pub Date : 2024-08-30 DOI:10.1039/D4SM00882K
Cuihong Ma, Cong Du, Qing Bo Tong, Xin Ning Zhang, Miao Du, Qiang Zheng and Zi Liang Wu
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Abstract

Incorporating associative interactions as the energy dissipation units has been recognized as an effective strategy to develop tough hydrogels. For hydrogen-bond associations, however, it is highly challenging to stabilize them under aqueous conditions. Although affording cooperativity can enhance and stabilize the hydrogen bonds, it usually requires stepwise polymerization to form these cooperative associations between different polymers and networks. Here, we report a series of tough supramolecular hydrogels with robust hydrogen-bond associations between grafted polymers that are synthesized by polymerization of a macromonomer of poly(N,N-dimethylacrylamide) (PDMAA) and a small monomer of methacrylic acid. The grafted chains of PDMAA form cooperative hydrogen bonds with the main chain of poly(methacrylic acid) (PMAAc), forming supramolecular hydrogels with high toughness and good stability. The tough and stiff hydrogels are in a glassy state, exhibit forced elastic deformation at room temperature, and remain stable over a wide pH range. In contrast, hydrogels prepared by the copolymerization of DMAA and MAAc are swollen and weak in water due to the lack of successive hydrogen donor/acceptor units and the absence of cooperative hydrogen bonds. In addition, these tough hydrogels exhibit good recyclability and shape memory properties, owing to the supramolecular nature of the network and the temperature-dependent mechanical properties. The influence of polymer structure on the associative interactions and macroscopic properties of the hydrogels should be informative for the design of tough soft materials with versatile applications.

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以合作氢键作为物理交联的聚(N,N-二甲基丙烯酰胺)接枝聚(甲基丙烯酸)韧性超分子水凝胶
将结合相互作用作为能量消耗单元已被公认为是开发韧性水凝胶的有效策略。然而,要在水性条件下稳定氢键结合却极具挑战性。虽然提供合作性可以增强和稳定氢键,但通常需要逐步聚合才能在不同聚合物和网络之间形成这些合作性结合。在此,我们报告了一系列坚韧的超分子水凝胶,这些水凝胶是通过聚(N,N-二甲基丙烯酰胺)(PDMAA)大单体和甲基丙烯酸小单体的聚合反应合成的,接枝聚合物之间具有牢固的氢键结合。接枝的 PDMAA 链与聚甲基丙烯酸主链(PMAAc)形成协同氢键,从而形成具有高韧性和良好稳定性的超分子水凝胶。韧性和硬度高的水凝胶呈玻璃态,在室温下表现出受迫弹性形变,并在较宽的 pH 值范围内保持稳定。相比之下,由 DMAA 和 MAAc 共聚制备的水凝胶由于缺乏连续的氢供体/受体单元和合作氢键,在水中会膨胀和变软。此外,由于网络的超分子性质和随温度变化的机械特性,这些坚韧的水凝胶具有良好的可回收性和形状记忆特性。聚合物结构对水凝胶的关联相互作用和宏观特性的影响,对设计具有多种应用的韧性软材料具有参考价值。
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来源期刊
Soft Matter
Soft Matter 工程技术-材料科学:综合
CiteScore
6.00
自引率
5.90%
发文量
891
审稿时长
1.9 months
期刊介绍: Where physics meets chemistry meets biology for fundamental soft matter research.
期刊最新文献
Back cover Chemo-mechanical model of cell polarization initiated by structural polarity. Controlling wall-particle interactions with activity. Viologen-based supramolecular crystal gels: gelation kinetics and sensitivity to temperature. Back cover
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