A Triply Negatively Curved Graphenic Macrocycle

Abstract Negatively curved nanographenes have attracted extensive research interest due to their unique topological characteristics. Although various saddle-shaped negatively curved nanographenes have been successfully synthesized, macrocycles with multiple negative curvatures remain rarely investigated. Herein, we present the synthesis and physical properties of a novel triply negatively curved graphenic macrocycle (TNM), which contains three negative curvature regions within its cyclic framework. Single-crystal X-ray diffraction unambiguously confirmed the triangular cyclic topology incorporating 12 heptagonal rings. Theoretical calculations of aromaticity reveal that the heptagonal rings exhibit nonaromatic character, while the TNM macrocycle possesses localized aromaticity. Furthermore, the electron-rich cavity of TNM enables stable host–guest interactions with C60 and C70, affording significantly stronger binding affinities than those of the parent negatively curved nanographene monomer. The present TNM macrocycle exhibits a distinctive topological architecture defined by multiple negative curvature regions, serving as a well-defined conjugated segment of carbon nanotori.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-09-11
DOI
https://doi.org/10.1021/jacs.6c11599
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
0.00

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article

A Triply Negatively Curved Graphenic Macrocycle

Wei Kang, Pingwu Du, Zheng Zhou, Xiaoyu Zhang et al.
Journal of the American Chemical Society
Synthesis and Properties of Aromatic Compounds
article

A Triply Negatively Curved Graphenic Macrocycle

Wei Kang, Pingwu Du, Zheng Zhou, Xiaoyu Zhang, Mingxin He, Xinyu Zhang, Heng Zhang, Jinyi Wang, Yong Ni
article en

Abstract

Abstract Negatively curved nanographenes have attracted extensive research interest due to their unique topological characteristics. Although various saddle-shaped negatively curved nanographenes have been successfully synthesized, macrocycles with multiple negative curvatures remain rarely investigated. Herein, we present the synthesis and physical properties of a novel triply negatively curved graphenic macrocycle (TNM), which contains three negative curvature regions within its cyclic framework. Single-crystal X-ray diffraction unambiguously confirmed the triangular cyclic topology incorporating 12 heptagonal rings. Theoretical calculations of aromaticity reveal that the heptagonal rings exhibit nonaromatic character, while the TNM macrocycle possesses localized aromaticity. Furthermore, the electron-rich cavity of TNM enables stable host–guest interactions with C60 and C70, affording significantly stronger binding affinities than those of the parent negatively curved nanographene monomer. The present TNM macrocycle exhibits a distinctive topological architecture defined by multiple negative curvature regions, serving as a well-defined conjugated segment of carbon nanotori.

Journal of the American Chemical Society
Tongji University (CN), Southern University of Science and Technology (CN), Jinzhong University (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, China Postdoctoral Science Foundation, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 21%
Synthesis and Properties of Aromatic Compounds
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