Answers are grounded in this paper and cite their sources.
A simple and practical synthesis of soluble hexa-peri-hexabenzocoronene (HBC) from readily available hexaphenylbenzene (HPB) is described. In this simple procedure, the substitution of the free para positions of the propeller-shaped HPB with tert-butyl groups and the oxidative cyclodehydrogenation to planar HBC is achieved in a one-pot reaction using ferric chloride both as a Lewis acid catalyst and as an oxidant in excellent yields. The ready availability of HBC allows the isolation of its pure cation-radical salt using a variety of chemical oxidants such as antimony pentachloride and triethyloxonium and nitrosonium hexachloroantimonate salts.
No takes yet. Share an insight, caveat, or question.
Rathore et al. (2003) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: