Abstract
Quinones constitute a big family of organic redox active compounds that are overwhelmingly involved in important physiological processes. The most important members in the class of quinones are, indeed, the plastoquinones and the coenzyme Q (CoQ) derivatives. Voltammetry of coenzyme Q family members attracts significant attention since 50 years ago. In this work, we refer to some of the most important voltammetric features of coenzyme Qs studied in aprotic and in aqueous media. While the redox chemistry of coenzyme Q members in non-aqueous aprotic organic solvents can be described by two consecutive one-electron transfer steps, more complex situation exists in the voltammetry of coenzyme Qs performed in aqueous media. Although it has been claimed for a while that the voltammetric processes of coenzyme Qs in aqueous solutions proceed via formation of semiquinone radical intermediate species, it has been recently proven that this can be not completely true. Intensive voltammetric and spectroscopic studies of coenzyme Q systems in buffered and non-buffered aqueous media revealed that hydrogen bonding between electrochemically created CoQ species and the water molecules plays an important role in stabilizing electrochemically generated species of these systems. We also pay attention to the amazing redox chemistry of coenzyme Qs in strong alkaline media, while we refer to the chemical features of novel coenzyme Q derivatives obtained under such conditions. Hints are presented about the antioxidant capacity of some of the novel hydroxylated coenzyme Q systems. Also, the possibility of these systems to bind and transfer earth-alkaline cations across biomimetic membranes is shortly elaborated. In the end, we refer to some relevant theoretical works that describe closely the voltammetric behavior of various coenzyme Q systems. We believe that this short review will contribute towards better understanding of the amazing chemistry of coenzyme Q derivatives.
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Acknowledgments
Rubin Gulaboski thanks the Goce Delcev University in Stip, Macedonia, for the financial support via the project: Metal-complexing and antioxidative properties of some new derivatives of Coenzyme Q-0 (2013–2016).
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Dedicated to the 65th birthday of our great friends and collaborators Dr. Milivoj Lovric and Dr. Sebojka Komorsky Lovric
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Gulaboski, R., Markovski, V. & Jihe, Z. Redox chemistry of coenzyme Q—a short overview of the voltammetric features. J Solid State Electrochem 20, 3229–3238 (2016). https://doi.org/10.1007/s10008-016-3230-7
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DOI: https://doi.org/10.1007/s10008-016-3230-7