Carbene-derived α-acyl formamidinium cations: organic molecules with readily tunable multiple redox processes

Abstract

A series of α-acyl formamidinium ions and their corresponding 1-electron reduced neutral radicals were synthesized, and their electrochemical properties were evaluated. These cations exhibit multi-electron redox processes that are highly electrochemically reversible at rapid scan rates (100 mV s⁻¹), and the redox potentials were readily tailored by up to ∼1.0 V, making them ideal candidates for organic radical-based charge storage materials.