π-Extended 9b-Boraphenalenes: Synthesis, Structure, and Physical Properties.

Boraphenalenes, compounds in which one carbon atom in the phenalenyl skeleton is replaced with a boron atom, have attracted attention for their solid-state and electronic structures; however, the construction of boraphenalene skeletons remains challenging because of the lack of suitable methods. Through this study, we showed that the tandem borylative cyclization of C 3 -symmetric dehydrobenzo[12]annulenes produces a new class of fully fused boron-atom-embedded polycyclic hydrocarbons possessing a 9b-boraphenalene skeleton. The obtained compounds exhibited high electron-accepting characteristics, and their two-step redox process was reversible in the reductive region, involving interconversion of 9b-boraphenalene between Hückel aromaticity and antiaromaticity. Notably, the benzo[ b ]fluorene-fused derivative exhibited a stepwise single-crystal-to-single-crystal (SCSC) phase transition triggered by thermal annealing. Intermolecular electron coupling calculation of the crystal structures suggested a significant improvement of charge transporting ability associated with the SCSC phase transition. Moreover, adequate photoconductivity was observed for the single crystals before and after the SCSC phase transition through flash photolysis-time-resolved microwave conductivity.