Multilevel chirality transfer and second harmonic generation in mesoscopic double helical supramolecular self-assemblies of fullerene enantiomers

Inducing chirality in the highly symmetric fullerene C<sub>60</sub> is an effective approach that leads to chiroptical responses over a wide range. However, the optically active expression of C<sub>60</sub> is a challenging research topic and multiscale modulation of fullerene chirality is still in its infancy. Herein, we synthesized a pair of fulleropyrrolidine enantiomers named R/S-MBA-C<sub>60</sub> with a monoclinic <i>P</i>2<sub>1</sub> chiral space group in the solid-state. Rare mesoscopic double helical supramolecular self-assemblies with distinctly opposite chirality have been obtained. Substantial π-π stacking and non-covalent interactions realize the chirality transfer and amplification across different scales, from the chiral carbon atom to the mesoscopic helix. Such fullerene-based double helical structures exhibit intense CD responses over an extremely wide range, from the UV-visible region and even up to the NIR region, and a SHG effect due the non-centrosymmetric molecular structure. This research develops an efficient approach to precisely modulate fullerene chirality and highlights the potential of chirality-based applications in fullerene science.

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Publication Details

Journal
Chemical Science
Published
2025-01-01
DOI
https://doi.org/10.1039/d5sc05354d
Citations
1
Primary Topic
Molecular Spectroscopy and Structure
Type
article
Field-Weighted Citation Impact
0.76

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article

Multilevel chirality transfer and second harmonic generation in mesoscopic double helical supramolecular self-assemblies of fullerene enantiomers

Yunlong Tao, Jingcheng Hao, Kaipeng Zhuang, Hongguang Li et al.
1 citations
Chemical Science
Molecular Spectroscopy and Structure
0.76
article

Multilevel chirality transfer and second harmonic generation in mesoscopic double helical supramolecular self-assemblies of fullerene enantiomers

Yunlong Tao, Jingcheng Hao, Kaipeng Zhuang, Hongguang Li, Qingfeng Zhang, Jingrui Li
article en
1 citations

Abstract

Inducing chirality in the highly symmetric fullerene C<sub>60</sub> is an effective approach that leads to chiroptical responses over a wide range. However, the optically active expression of C<sub>60</sub> is a challenging research topic and multiscale modulation of fullerene chirality is still in its infancy. Herein, we synthesized a pair of fulleropyrrolidine enantiomers named R/S-MBA-C<sub>60</sub> with a monoclinic <i>P</i>2<sub>1</sub> chiral space group in the solid-state. Rare mesoscopic double helical supramolecular self-assemblies with distinctly opposite chirality have been obtained. Substantial π-π stacking and non-covalent interactions realize the chirality transfer and amplification across different scales, from the chiral carbon atom to the mesoscopic helix. Such fullerene-based double helical structures exhibit intense CD responses over an extremely wide range, from the UV-visible region and even up to the NIR region, and a SHG effect due the non-centrosymmetric molecular structure. This research develops an efficient approach to precisely modulate fullerene chirality and highlights the potential of chirality-based applications in fullerene science.

Chemical ScienceVol. 16(42)
Shandong University (CN), Wuhan University (CN)
Shandong University, National Natural Science Foundation of China
Openalex Percentile: Top 25%
Molecular Spectroscopy and Structure
0.76
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Multilevel chirality transfer and second harmonic generation in mesoscopic double helical supramolecular self-assemblies of fullerene enantiomers — Yunlong Tao, Jingcheng Hao, et al. · Chemical Science (2025) | TGRS Research Map | TGRS