Synthesis and electro-spectroelectrochemistry of ferrocenyl naphthaquinones

Abstract

Abstract A practical approach to ferrocenyl naphthaquinone derivatives involving thermal rearrangement of variously substituted 4-aryl-4-hydroxycyclobutenones was described. The reaction of 3-ferrocenyl-4-isopropoxy-3-cyclobutene-1,2-dione with different aryl lithiums gave the corresponding 4-aryl-4-hydroxycyclobutenones, which were heated in p -xylene at reflux open to the air to yield ferrocenyl naphthaquinones. The redox chemistry of the ferrocenyl naphthaquinones was studied by electrochemical and in situ spectroelectrochemical techniques in CH 2 Cl 2 solution and in CH 3 CN solution with water, weak and strong acidic additives. Ferrocenyl naphthaquinones displayed reversible two reduction processes involving semiquinone radical anion (Fc–snq − ), dianion (Fc–nq 2− ) species and a one-electron oxidation process based on the ferrocenium/ferrocene (Fc + –nq/Fc–nq) couple in CH 2 Cl 2 . The redox reaction mechanism of the ferrocenyl naphthaquinones in the presence of the additives proceeded via hydrogen bonding or proton-coupled electron transfer. Effects of the substituents on the reduction potentials and intramolecular charge-transfer bands of ferrocenyl naphthaquinones were also discussed.