Synthesis, structure and π-expansion of tris(4,5-dehydro-2,3:6,7-dibenzotropone)

Beilstein J Org Chem. 2025 Jan 2:21:1-7. doi: 10.3762/bjoc.21.1. eCollection 2025.

Abstract

The polycyclic skeleton of tris(4,5-dehydro-2,3:6,7-dibenzotropone) is a key structural fragment in carbon schwarzites, a theoretical form of negatively curved carbon allotrope. This report presents a new synthesis of this compound using a Ni-mediated Yamamoto coupling reaction and structural analysis of it with X-ray crystallography. Interestingly, it is observed that tris(4,5-dehydro-2,3:6,7-dibenzotropone) crystallized from its solution in hexane resulting in colorless and yellow crystal polymorphs, where it adopts conformations of approximate C s and C 2 symmetry, respectively. Furthermore, expanding its π-skeleton through the Barton-Kellogg and Scholl reactions led to the successful synthesis of a curved polycyclic arene containing three heptagons and two pentagons.

Keywords: Scholl reaction; Yamamoto coupling; carbon schwarzites; polycyclic arenes; seven-membered carbocycle.

Grants and funding

We acknowledge the financial support provided by the Research Grants Council of Hong Kong (GRF 14300323) and the State Key Laboratory of Synthetic Chemistry.