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Unusual Structures of Interpolyelectrolyte Complexes: Vesicles and Perforated Vesicles

机译:聚电解质复合物的异常结构:囊泡和穿孔的囊泡。

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摘要

By means of computer simulation and analytical theory, we first demonstrated that the interpolyelectrolyte complexes in dilute solution can spontaneously form hollow spherical particles with thin continuous shells (vesicles) or with porous shells (perforated vesicles) if the polyions forming the complex differ in their affinity for the solvent. The solvent was considered good for the nonionic groups of one macroion and its quality was varied for the nonionic groups of the other macroion. It was found that if the electrostatic interactions are weak compared to the attraction induced by the hydrophobicity of the monomer units, the complex in poor solvent tends to form “dense core–loose shell” structures of different shapes. The strong electrostatic interactions favor the formation of the layered, the hollow, and the filled structured morphologies with the strongly segregated macroions. Vesicles with perforated walls were distinguished as the intermediate between the vesicular and the structured solid morphologies. The order parameter based on the spherical harmonics expansion was introduced to calculate the pore distribution in the perforated vesicles depending on the solvent quality. The conditions of the core–shell and hollow vesicular-like morphologies formation were determined theoretically via the calculations of their free energy. The results of the simulation and theoretical approaches are in good agreement.
机译:通过计算机模拟和分析理论,我们首先证明了稀溶液中的聚电解质间复合物可以自发​​形成具有薄连续壳(囊泡)或多孔壳(穿孔囊泡)的空心球形颗粒(如果形成复合物的聚离子的亲和力不同)用作溶剂。该溶剂被认为对于一个大分子离子的非离子基团是好的,而对于另一种大分子离子的非离子基团,其质量是变化的。已经发现,如果与单体单元的疏水性所引起的吸引力相比,如果静电相互作用较弱,则在不良溶剂中的络合物往往会形成不同形状的“致密核-松散壳”结构。强烈的静电相互作用有利于形成层状,中空和填充的结构形态以及强分离的大分子。具有穿孔壁的囊泡被区分为囊泡和结构化固体形态之间的中间。引入了基于球谐展开的有序参数,以根据溶剂质量计算多孔小泡中的孔分布。通过计算其自由能,理论上确定了核-壳和中空囊状形态形成的条件。仿真结果与理论方法吻合良好。

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