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

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 elusi...

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Veröffentlicht in:Journal of the American Chemical Society 2023-10, Vol.145 (40), p.22176-22183
Hauptverfasser: Li, Chong-Yang, Xu, Han, Cheng, Pei-Ming, Du, Ming-Hao, Long, La-Sheng, Zheng, Lan-Sun, Kong, Xiang-Jian
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container_end_page 22183
container_issue 40
container_start_page 22176
container_title Journal of the American Chemical Society
container_volume 145
creator Li, Chong-Yang
Xu, Han
Cheng, Pei-Ming
Du, Ming-Hao
Long, La-Sheng
Zheng, Lan-Sun
Kong, Xiang-Jian
description 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 f–f 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.
doi_str_mv 10.1021/jacs.3c08257
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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 f–f 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. 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