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.
Authors
- Yunlong Tao
- Jingcheng Hao (ORCID: https://orcid.org/0000-0002-9760-9677)
- Kaipeng Zhuang
- Hongguang Li (ORCID: https://orcid.org/0000-0002-5773-5003)
- Qingfeng Zhang (ORCID: https://orcid.org/0000-0002-7004-9040)
- Jingrui Li (ORCID: https://orcid.org/0000-0003-0348-068X)
Institutions
- Shandong University (CN)
- Wuhan University (CN)
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
Funders
- Shandong University
- National Natural Science Foundation of China