Transformation of a benzocorrole isomer into pyrrole-containing polycyclic molecules <i>via</i> copper-mediated cleavage and annulation
Copper-facilitated oxidative ring cleavage, followed by ring fusion of a corrole isomer, produced a pyrrole-embedded polycyclic molecule. This molecule demonstrates near-infrared absorption and possesses p-type semiconducting properties.
Authors
- Shigeki Mori (ORCID: https://orcid.org/0000-0001-6731-2357)
- Hiroyuki Furuta (ORCID: https://orcid.org/0000-0002-3881-8807)
- Biju Basumatary (ORCID: https://orcid.org/0000-0003-1866-1686)
- Tatsuya Mori (ORCID: https://orcid.org/0009-0001-2208-6955)
- Masatoshi Ishida (ORCID: https://orcid.org/0000-0002-1117-2188)
- Daisuke Kawaguchi (ORCID: https://orcid.org/0000-0001-8930-039X)
- Takuma Yasuda (ORCID: https://orcid.org/0000-0003-1586-4701)
- Tatsuki Abe (ORCID: https://orcid.org/0000-0001-9923-8032)
- Shiro Oka
- S. Yada
Institutions
- Kyushu University (JP)
- Ehime University (JP)
- Tokyo Metropolitan University (JP)
Publication Details
- Journal
- Organic Chemistry Frontiers
- Published
- 2024-12-11
- DOI
- https://doi.org/10.1039/d4qo02145b
- Citations
- 1
- Primary Topic
- Porphyrin and Phthalocyanine Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.12