聚电解质
凝聚
不对称
序列(生物学)
静电学
相(物质)
电荷(物理)
化学
化学物理
生物分子
材料科学
纳米技术
色谱法
物理
聚合物
有机化学
物理化学
生物化学
量子力学
作者
Xu Chen,Er‐Qiang Chen,Shuang Yang
出处
期刊:Macromolecules
[American Chemical Society]
日期:2022-12-20
卷期号:56 (1): 3-14
被引量:13
标识
DOI:10.1021/acs.macromol.2c01205
摘要
The complex coacervation of oppositely charged polyelectrolytes is an important issue, which is relevant to many biological and industrial applications. While various biomolecules have been observed to form hierarchical multiphase structures in cells, its mechanism is still not fully understood. Here, we theoretically study the complex coacervation between the polyanion C and polycations A and B in solution and focus on the influence of charge sequence along the polyions on the multiphase coacervation. The electrostatic free energy is calculated with random phase approximation, and the phase diagrams are constructed by using the convex hull algorithm. It is revealed that the large asymmetry of charge patterns between A and B chains may induce the multiphase separation, driving the formation of two condensed phases, AC coacervate and BC coacervate, coexisting with a dilute phase. On the basis of our result, we propose a good criterion to determine if multiphase separation occurs or not. Furthermore, we analyze the effect of charge sequence of polyanion C as well as the addition of salt on the multiphase coacervation. This work provides insights into the underlying physics of sequence-dependent electrostatic interactions and the design of complex coacervates of polyelectrolyte mixtures.
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