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左旋还是右旋胆甾相液晶?这是一个关于螺旋手性和卷曲度的问题。

Left or right cholesterics? A matter of helix handedness and curliness.

作者信息

Frezza Elisa, Ferrarini Alberta, Kolli Hima Bindu, Giacometti Achille, Cinacchi Giorgio

机构信息

Dipartimento di Scienze Chimiche, Università di Padova, via F. Marzolo 1, 35131 Padova, Italy.

出版信息

Phys Chem Chem Phys. 2014 Aug 14;16(30):16225-32. doi: 10.1039/c4cp01816h.

Abstract

Using an Onsager-like theory, we have investigated the relationship between the morphology of hard helical particles and the features (pitch and handedness) of the cholesteric phase that they form. We show that right-handed helices can assemble into right- (R) and left-handed (L) cholesterics, depending on their curliness, and that the cholesteric pitch is a non-monotonic function of the intrinsic pitch of particles. The theory leads to the definition of a hierarchy of pseudoscalars, which quantify the difference in the average excluded volume between pair configurations of helices having (R) and (L)-skewed axes. The predictions of the Onsager-like theory are supported by Monte Carlo simulations of the isotropic phase of hard helices, showing how the cholesteric organization, which develops on scales longer than hundreds of molecular sizes, is encoded in the short-range chiral correlations between the helical axes.

摘要

利用一种类昂萨格理论,我们研究了硬螺旋粒子的形态与它们所形成的胆甾相的特征(螺距和手性)之间的关系。我们表明,右手螺旋可以根据其卷曲程度组装成右手(R)和左手(L)胆甾相,并且胆甾相螺距是粒子固有螺距的非单调函数。该理论引出了一系列赝标量的定义,这些赝标量量化了具有(R)和(L)倾斜轴的螺旋对构型之间平均排除体积的差异。类昂萨格理论的预测得到了硬螺旋各向同性相的蒙特卡罗模拟的支持,显示了在比数百个分子尺寸更长的尺度上形成的胆甾相组织是如何编码在螺旋轴之间的短程手性相关性中的。

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