Accessing Boron-Doped Pentaphene Analogues from 12-Boradibenzofluorene

Borole-doped polycyclic aromatic hydrocarbons (PAHs) have garnered attention in recent years due to their attractive photophysical properties and potential utility in electronic devices. In this work, a borole-doped PAH, 12-boradibenzofluorene, is synthesized and formal intermolecular nitrene and oxygen atom insertion reactions were employed to access 1,2-azaborine- and 1,2-oxaborine-containing analogues of the carbonaceous PAH pentaphene. Iodosobenzene is established as a versatile reagent for oxygen atom insertion reactions into a variety of borole species to access 1,2-oxaborine systems.

Automated summary

Borole-doped polycyclic aromatic hydrocarbons (PAHs) have been synthesized and studied in this work. Intermolecular nitrene and oxygen atom insertion reactions were used to access 1,2-azaborine- and 1,2-oxaborine-containing analogues. Iodosobenzene was established as a versatile reagent for oxygen atom insertion reactions into various borole species to access 1,2-oxaborine systems.