Electrochemical Investigation of Symmetric Aminoquinones

Quinones have a wide range of valuable properties and potential applications in medicinal chemistry, materials science,
optoelectronic devices, and batteries. Molecular redesign using different functional groups, like amines, can optimize their
properties and prevent undesired side reactions. However, the synthesis of aminoquinones can be particularly challenging at times,
and there is a need for simple and efficient routes to access these compounds without metal catalysts or halogenated starting
materials. Here, we demonstrate the synthesis and electrochemical characterization of a series of aminoquinones derived from
renewable sources, namely vanillin or 2-methoxyhydroquinone. We employ a series of primary and secondary amines, varying in
their electronic situation as well as steric demand. Depending on the type of starting material, either the desired aminoquinone or
the related Schiff-base adduct was obtained. The aminoquinones were further explored towards their stability at different pH
values. At extreme pH values, the deeply colored aminoquinones decompose, accompanied by decolorization of the solutions
within a few minutes (pH 14) or hours (pH 1). At intermediate pH values (3–8) the aminoquinones are stable upon storage in
solution, where they feature a quasi-reversible redox chemistry and fast, diffusion limited kinetics.