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从螺旋到晶体:双螺旋结构中手性的多尺度表征

From Helices to Crystals: Multiscale Representation of Chirality in Double-Helix Structures.

作者信息

Li Chong-Yang, Xu Han, Cheng Pei-Ming, Du Ming-Hao, Long La-Sheng, Zheng Lan-Sun, Kong Xiang-Jian

机构信息

Collaborative Innovation Center of Chemistry for Energy Materials, State Key Laboratory of Physical Chemistry of Solid Surfaces, and Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.

出版信息

J Am Chem Soc. 2023 Oct 11;145(40):22176-22183. doi: 10.1021/jacs.3c08257. Epub 2023 Oct 1.

Abstract

Single crystals with chiral shapes aroused the interest of chemists due to their fascinating polarization rotation properties. Although the formation of large-scale spiral structures is considered to be a potential factor in chiral crystals, the precise mechanism behind their formation remains elusive. Herein, we present a rare phenomenon involving the multitransfer and expression of chirality at micro-, meso-, and macroscopic levels, starting from chiral carbon atoms and extending to the double-helical secondary structure, ultimately resulting in the chiral geometry of crystals. The assembly of the chiral double helices is facilitated by the dual characteristics of amide groups derived from amino acids, which serve as both hydrogen bond donors and receptors, similar to the assembly pattern observed in DNA. Crystal face analysis and theoretical morphology reveal two critical factors for the mechanism of the chiral crystal: inherent intrinsically symmetrical distribution of crystal faces and their acquired growth. Importantly, the magnetic circular dichroism (MCD) study reveals the strong magneto-optical response of the hypersensitive ff transition in the UV-vis-NIR region, which is much stronger than previously observed signals. Remarkably, an external magnetic field can reverse the CD signal. This research highlights the potential of lanthanide-based chiral helical structures as promising magneto-optical materials.

摘要

具有手性形状的单晶因其迷人的偏振旋转特性引起了化学家的兴趣。尽管大规模螺旋结构的形成被认为是手性晶体形成的一个潜在因素,但其形成背后的确切机制仍然难以捉摸。在此,我们展示了一种罕见的现象,涉及从手性碳原子开始,延伸到双螺旋二级结构,最终导致晶体手性几何形状的微观、介观和宏观层面的手性多转移和表达。手性双螺旋的组装得益于氨基酸衍生的酰胺基团的双重特性,这些基团既作为氢键供体又作为受体,类似于在DNA中观察到的组装模式。晶面分析和理论形态学揭示了手性晶体形成机制的两个关键因素:晶面固有的内在对称分布及其获得的生长。重要的是,磁圆二色性(MCD)研究揭示了紫外-可见-近红外区域中超灵敏的ff跃迁的强磁光响应,这比以前观察到的信号要强得多。值得注意的是,外部磁场可以反转CD信号。这项研究突出了基于镧系元素的手性螺旋结构作为有前途的磁光材料的潜力。

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