Ring-Expanding Rearrangement of Benzo-Fused Tris-Cycloheptenylenes towards Nonplanar Polycyclic Aromatic Hydrocarbons.

A strongly twisted benzo-fused tris-cycloheptenylene, containing three dibenzosuberenone units fused to a common benzene ring, was subjected to Ramirez olefination and subsequent palladium-catalyzed Suzuki-Miyaura cross-coupling with 4-substituted phenylboronic acids. The high steric demand within the overcrowded, benzene-rich benzo-fused tris-cycloheptenylenes enforced an unprecedented 1,2-rearrangement upon π-extension during the Suzuki coupling reaction. According to crystal structure analysis, the resulting negatively curved polycyclic aromatic hydrocarbons consist of two heptagons and one octagon surrounding a central benzene ring as a result of strain release. In the solid state, the materials exhibit a blue to blue-green fluorescence with increased quantum yields and a hypsochromic shift of the emission maxima compared to their respective solutions.