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Self-Assembled Chiral Superstructures Composed of Rigid Achiral Molecules and Molecular Scale Chiral Induction by Dopants

机译:刚性非手性分子的自组装手性上层结构和掺杂剂的分子尺度手性诱导

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摘要

We explore the phase behavior of a rigid achiral bent-core model system. Nematic and smectic phases form at higher densities, whereas micelles and columns composed of chiral clusters of these molecules self-assemble at lower densities. No nucleation mechanism requiring transient chirality is possible in the formation of these chiral superstructures due to the rigid achiral nature of the substituents. We show the chiral micelles are minima of the potential energy surface using energy minimization and parallel tempering simulations. Chiral dopants were found to induce the system to adopt a consistent chiral twist direction, the first molecular scale computer simulation of this effect.
机译:我们探索刚性非手性弯曲核心模型系统的相行为。向列相和近晶相以较高的密度形成,而由这些分子的手性簇组成的胶束和柱以较低的密度自组装。由于取代基的刚性非手性,在这些手性超结构的形成中,要求瞬态手性的成核机理是不可能的。我们使用能量最小化和平行回火模拟显示手性胶束是势能面的最小值。发现手性掺杂剂可以诱导系统采用一致的手性扭曲方向,这是该效应的首个分子计算机模拟。

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