Abstract
A novel design of electroactive components of rechargeable organic batteries based on stable verdazyl radicals bearing various substituents is proposed. 3-Positioned aromatic substituents at the verdazyl moiety affect the reduction potentials and almost do not affect the oxidation potential, while 1-positioned aromatic substituents affect contrariwise the oxidation potential of this radical without any influence on the reduction potential. The acquired electrochemical data allowed us to reveal the structure—potential relationship for the cathodic and anodic processes, which provided the design of triarylverdazyl radicals possessing record-breaking parameters of the “electrochemical gap”.
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Based on the materials of the XXI Mendeleev Congress on General and Applied Chemistry (September 9–13, 2019, St. Petersburg, Russia).
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1321–1328, July, 2020.
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Kostryukov, S.G., Chernyaeva, O.Y., Tanaseichuk, B.S. et al. Triarylverdazyl radicals as promising redox-active components of rechargeable organic batteries. Russ Chem Bull 69, 1321–1328 (2020). https://doi.org/10.1007/s11172-020-2905-5
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DOI: https://doi.org/10.1007/s11172-020-2905-5