Fully conjugated azacorannulene dimer as large diaza[80]fullerene fragment

A fully conjugated azacorannulene dimer with a large pi-surface (76 pi system) was successfully synthesized from a fully conjugated bifunctional polycyclic aromatic azomethine ylide. This molecule represents an example of diaza[80]fullerene (C78N2) fragment molecule bearing two internal nitrogen atoms. X-ray crystallography analysis shows its boat-shaped structure with two terminal azacorannulenes bent in the same direction. The molecular shape leads to unique selective association with a dumbbell-shaped C-60 dimer (C-120) over C-60 through shape recognition. Owing to its large pi-surface and a narrow HOMO-LUMO gap, the azacorannulene dimer exhibits red fluorescence with a quantum yield of up to 31%. The utilization of the fully conjugated bifunctional azomethine ylide is a powerful method for the bottom-up synthesis of large multiazafullerene fragments, providing a step towards the selective total synthesis of multiazafullerenes.

Automated summary

A fully conjugated azacorannulene dimer with a large pi-surface has been successfully synthesized, which exhibits unique selective association with a dumbbell-shaped C-60 dimer and shows high quantum yield of red fluorescence. The utilization of a fully conjugated bifunctional azomethine ylide for the synthesis of large multiazafullerene fragments is a powerful method and has significant implications for the selective total synthesis of multiazafullerenes.