合理设计
聚合物
分子间力
单体
相(物质)
纳米技术
化学
材料科学
化学物理
分子动力学
工作流程
非共价相互作用
计算机科学
材料设计
组合化学
分子
计算化学
设计要素和原则
相变
表面力仪
作者
Timo N. Schneider,Suiying Ye,Nicola Carrara,Umberto Capasso Palmiero,Matteo Salvalaglio,Paolo Arosio
出处
期刊:Macromolecules
[American Chemical Society]
日期:2025-10-08
卷期号:58 (20): 11192-11199
标识
DOI:10.1021/acs.macromol.5c01394
摘要
Zwitterionic polymers are emerging as promising candidates for forming fluid-like coacervates with desirable characteristics, including antifouling capabilities, stimulus responsiveness, and biocompatibility. These attributes make them particularly appealing for applications in the biomedical field, including bioseparation, biochemical analysis, and diagnostics. However, there are currently no clear guiding principles for predicting the phase separation behavior of zwitterionic polymers and informing the design of novel phase-separating polymers. In this study, we develop a workflow that combines molecular dynamics simulations, theory, and experiments to predict the phase separation propensity of zwitterionic polymers, as well as the material properties of the resulting coacervates. We validate our simulation-based workflow as a predictive tool by synthesizing new zwitterionic polymers that undergo no phase separation, liquid-liquid phase separation, or liquid-gel phase separation. Beyond their predictive power, we show that molecular simulations provide insights into the attractive homotypic intermolecular interactions mediated by distinct functional groups, rationalizing the large differences observed between zwitterionic monomers that exhibit minimal structural variations. Our approach provides valuable insights into the molecular principles governing the phase separation of distinct zwitterionic polymers, with important implications for the design of their materials.
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