An Electron-Deficient Azacoronene Obtained by Radial pi Extension

摘要

A hexapyrrolohexaazacoronene derivative containing 37 fused rings, the largest such system to date, was obtained from a naphthalenomonoimide-pyrrole hybrid in a concise and efficient synthesis. This large heterocycle is electron-deficient and shows extended redox activity, spanning at least 13 oxidation levels, but is otherwise chemically stable. Radial expansion of the pi system creates a chromophore characterized by strong fluorescence and solvatochromism in the neutral state, and strong near-infrared absorption in the charged states. Additionally, the enlarged and ruffled aromatic surface supports a unique self-assembly mode in the crystal, leading to the formation of highly solvated organic clathrates.