Reconfigurable liquids enabled by dynamic covalent chemistry

Aggregate Pub Date : 2024-07-12 DOI:10.1002/agt2.621
Kaijuan Li, Yuzheng Luo, Yunhui Wen, Wenrui Shan, Shaowei Shi
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Abstract

Nanoparticle surfactants (NPSs) that form via the reversible non‐covalent interactions between nanoparticles (NPs) and polymer ligands at the oil‐water interface have received great attention in constructing structured liquids with unique stimuli‐responsiveness. Introducing dynamic covalent interactions to generate NPSs is expected to achieve a balance between high mechanical strength and dynamic responsiveness of the interfacial assemblies. Here, we present the formation, assembly, and jamming of a new type of NPS by the co‐assembly between polydopamine NPs (PDA NPs) and poly(styrene‐co‐methacrylamidophenylboronic acid) at the oil‐water interface. Dynamic covalent boronate ester bonds form in situ at the interface and show multiple responsiveness when applying stimuli such as pH, H2O2, and temperature, allowing the controlled assembly/jamming of NPSs and reconfiguration of liquid constructs. Due to the photothermal property of PDA NPs, the temperature responsiveness of boronate ester bonds can also be triggered by irradiating the biphasic system with near‐infrared (NIR) light. Moreover, when bringing two droplets encapsulated with NPSs into contact and irradiating the contact area by NIR, thermal welding of droplets can be realized, offering a straightforward to construct droplet networks and modular liquid devices.

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通过动态共价化学实现可重构液体
纳米粒子表面活性剂(NPSs)是通过纳米粒子(NPs)与聚合物配体在油水界面上的可逆非共价相互作用形成的,在构建具有独特刺激响应性的结构液体方面受到了极大关注。引入动态共价相互作用生成 NPS,有望在高机械强度和界面组装的动态响应性之间实现平衡。在此,我们介绍了聚多巴胺 NPs(PDA NPs)与聚(苯乙烯-共甲基丙烯酰胺苯基硼酸)在油水界面上共同组装形成、组装和干扰新型 NPS 的情况。动态共价硼酸酯键在界面上原位形成,并在 pH 值、H2O2 和温度等刺激下显示出多种响应性,从而实现了 NPS 的可控组装/干扰和液体结构的重新配置。由于 PDA NPs 具有光热特性,用近红外光照射双相体系也能触发硼酸酯键的温度响应。此外,当两个用 NPSs 封装的液滴接触并用近红外光照射接触区域时,液滴的热焊接就可以实现,这为构建液滴网络和模块化液体装置提供了直接的途径。
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