Dibenzo[ <i>a,o</i> ]picene: A Semiconducting Nonplanar Heptacene Isomer
We report a concise two-step synthesis of the elusive heptacene isomer dibenzo[<i>a,o</i>]picene via regioselective Mallory photocyclization of a bis(stilbenyl)phenanthrene precursor. DFT calculations rationalize the observed regioselectivity and confirm the aromatic, highly stable framework. Dibenzo[<i>a,o</i>]picene exhibits a 2.98 eV optical band gap, reversible oxidation, and a low-lying HOMO. Single-crystal X-ray analysis reveals one-dimensional π-stacking (3.31 Å). Single-crystal OFETs display p-type hole mobilities of 3.2 × 10<sup>-3</sup> cm<sup>2</sup> V<sup>-1</sup> s<sup>-1</sup>, establishing this long-sought isomer as a promising air-stable semiconductor.
Authors
- Zekang Ma
- Y. Chen (ORCID: https://orcid.org/0009-0004-0540-7931)
- Yao Ze-Fan
- Jian Pei
- Yi Wang (ORCID: https://orcid.org/0000-0002-8235-2952)
- Huijie Wei
- Zexin Jin
Institutions
- Peking University (CN)
- Westlake University (CN)
- Beijing National Laboratory for Molecular Sciences (CN)
- Institute for the Future (US)
- Zhejiang University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-01-08
- DOI
- https://doi.org/10.1021/acs.orglett.5c04940
- Primary Topic
- Synthesis and Properties of Aromatic Compounds
- Type
- article
- Field-Weighted Citation Impact
- 0.00