乙二醇
侧链
高分子化学
嫁接
甲基丙烯酸酯
聚合物
壳聚糖
乙烯
化学工程
材料科学
共聚物
化学
有机化学
催化作用
工程类
作者
Ming Lei,Haiyan Zhu,Zhixiang Cai,Zhehui Jin,Jiangen Xu,Hui Mao,Yanjun He
出处
期刊:Macromolecules
[American Chemical Society]
日期:2025-08-28
卷期号:58 (17): 8990-9009
标识
DOI:10.1021/acs.macromol.5c00188
摘要
Chitosan-based thermoresponsive graft polymers serve as promising functional materials for sustainable and intelligent applications, while their temperature-induced phase transition mechanism associated with the two components of the backbone and side chain remains elusive. Here, we perform molecular dynamics simulations from 300 to 390 K to explore the lower critical solution temperature (LCST) behavior of a graft polymer (CMCS-g-OEGMA) with carboxymethyl chitosan (CMCS) as the backbone and oligo(ethylene glycol) methyl ether methacrylate (OEGMA) as the side chain. The simulations show that a high grafting density (>0.5, especially when all structural units are fully occupied) is essential for LCST transition, at which a structural change of single-chain extended-to-collapsed and multichain dispersed-to-aggregated, a conformational transition from syn to anti, and a solvation structure disruption in cage-like first and second shells happen above LCST. The driving effect for this transition comes from the hydrophobic interaction of OEGMA brushes, energetically diminishing the original stabilizing interactions of the exo-anomeric effect, intramolecular hydrogen-bond networks, and steric solvation shells along the backbone, consequently enabling the phase transition stabilized by reformed intramolecular interactions in the rearranged collapsed chain structure.
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