Abstract
1,2-Di(6-azulenyl)tetraphenylbenzenes and (6-azulenyl)pentaphenylbenzenes were synthesized by Diels–Alder reaction of di(6-azulenyl)acetylenes and 6-(phenylethynyl)azulenes with tetraphenylcyclopentadienone. Mono(6-azulenyl)benzenes exhibited a reduction wave upon cyclic voltammetry (CV). In contrast to the benzene derivatives, di(6-azulenyl)benzenes showed a two-step reduction wave at similar potential region upon CV, which revealed the formation of dianions stabilized by 6-azulenyl substituents under electrochemical reduction conditions.
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