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Crystallization of helical oligomers with chirality selection.I.A molecular dynamics simulation for bare helix

机译:具有手性选择的螺旋低聚物的结晶I.裸螺旋的分子动力学模拟

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Helical polymers often exhibit pronounced chirality recognition during crystallization.By molecular dynamics simulation,we have already shown that the helical polymers crystallize with or without marked chirality selection depending on structural details of the polymer molecules.We have there classified the helical polymers into two categories:the bare helices made of only backbone atoms which show rather tolerant chirality selection,and the general helices with large side groups showing strict chirality recognition.Polymer crystallization is in general largely hampered and retarded by slow dynamics of the entangled chains,and therefore short helical oligomers are very suitable models for studying the chiral crystallization.We here report on molecular simulations of crystallization in the bare helical oligomer molecules by the use of Monte Carlo and molecular dynamics simulations.First we confirm the low temperature chiral crystal phase and the reversible order-disorder transition.We also observe frequent inversions of the helical sense,and the helix reversal defects propagating along the chains.Then we investigate crystallization from the melt into the chiral crystal phase.We find that the crystallization rate depends very sensitively on the degree of undercooling.The crystallization is found to be the first order transition that conforms well to the traditional picture of crystal growth in small molecules.Even when the crystallization directly into the chiral crystal phase is conducted,marked chirality selections are not observed at the early stage of crystallization;the chains adhere to the crystal surfaces selecting their helical senses rather at random resulting in racemic crystallites.The isothermal crystallization for a sufficiently long time,however,yields lamellar crystals composed of well-developed chiral domains,the growth of which seems to be accomplished through the transition back into the ordered chiral crystal phase.
机译:螺旋聚合物在结晶过程中通常表现出明显的手性识​​别。通过分子动力学模拟,我们已经显示了根据聚合物分子的结构细节,无论是否选择明显的手性,都会结晶的聚合物。我们将螺旋聚合物分为两类:仅由主链原子构成的裸螺旋显示出相当宽容的手性选择,而带有大侧基的普通螺旋则显示出严格的手性识别。聚合物的结晶通常在很大程度上受缠结链的缓慢动力学的阻碍和阻滞,因此,短螺旋低聚物是研究手性结晶的非常合适的模型。本文通过蒙特卡罗方法和分子动力学模拟报告了裸螺旋低聚物分子的结晶分子模拟。首先,我们确认了低温手性结晶相和可逆有序无序过渡我们还观察到了螺旋方向的频繁反转,并且螺旋反转缺陷沿着链传播。然后,我们研究了从熔体到手性晶相的结晶过程。我们发现结晶速度非常敏感地取决于过冷度。被发现是与小分子晶体生长的传统图景非常吻合的一阶跃迁。即使直接进行手性结晶相的结晶,在结晶的早期阶段也没有观察到明显的手性选择;链附着等温结晶足够长的时间,但会产生由发达的手性域组成的层状晶体,其生长似乎是通过向后过渡而完成的进入有序的手性晶体相。

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