Carbene Zipper Reaction for Cascade π-Extension

The unique electronic, thermal, and mechanical properties of nanographenes structured with polycyclic aromatic hydrocarbons (PAHs) can be finely tuned via modulation of the π-length, π-width, π-shape, π-edge, and π-curvature topology. However, the programmable construction of such architectures remains a formidable challenge, drastically hindering the systematic exploration of structure-property relationships in graphene-based materials. In this study, a cascade π-extension strategy has been established for the precise synthesis of PAHs through a copper-catalyzed domino carbene transfer process, enabling determinate structural control with tunable lengths, facilitating the construction of versatile twisted π-systems with local aromaticity variations.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-10-13
DOI
https://doi.org/10.1021/jacs.5c14209
Citations
1
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
0.94
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article

Carbene Zipper Reaction for Cascade π-Extension

Leiyang Bai, Xuefeng Jiang, Hongxu Lv
1 citations
Journal of the American Chemical Society
Synthesis and Properties of Aromatic Compounds
0.94
article

Carbene Zipper Reaction for Cascade π-Extension

Leiyang Bai, Xuefeng Jiang, Hongxu Lv
article en
1 citations

Abstract

The unique electronic, thermal, and mechanical properties of nanographenes structured with polycyclic aromatic hydrocarbons (PAHs) can be finely tuned via modulation of the π-length, π-width, π-shape, π-edge, and π-curvature topology. However, the programmable construction of such architectures remains a formidable challenge, drastically hindering the systematic exploration of structure-property relationships in graphene-based materials. In this study, a cascade π-extension strategy has been established for the precise synthesis of PAHs through a copper-catalyzed domino carbene transfer process, enabling determinate structural control with tunable lengths, facilitating the construction of versatile twisted π-systems with local aromaticity variations.

Journal of the American Chemical SocietyVol. 147(42)
Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN), East China Normal University (CN), Henan Normal University (CN)
Openalex Percentile: Top 21%
Synthesis and Properties of Aromatic Compounds
0.94
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