Synthesis of the Unknown Indeno[1,2‐a]fluorene Regioisomer: Crystallographic Characterization of Its Dianion

Of the five possible indenofluorene regioisomers, examples of a fully conjugated indeno[1,2-a]fluorene scaffold have so far remained elusive. This work reports the preparation and characterization of 7,12-dimesitylindeno[1,2-a]fluorene as a highly reactive species. Experimental and computational data support the notion of a molecule with pronounced diradical character that exists in a triplet ground state. As such, both NICS and ACID calculations suggest that the indeno[1,2-a]fluorene scaffold is weakly Baird aromatic. Reduction of the unstable red solid with Cs metal produces the dianion of the title compound, from which single crystals could be obtained and X-ray data acquired, thus fully corroborating the proposed indeno[1,2-a]fluorene hydrocarbon core.