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Electrochemistry and Stability of 1,1′-Ferrocene-Bisphosphonates

[Image: see text] Here, we investigate the electrochemical properties and stability of 1,1′-ferrocene-bisphosphonates in aqueous solutions. (31)P NMR spectroscopy enables to track decomposition at extreme pH conditions revealing partial disintegration of the ferrocene core in air and under an argon...

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Detalles Bibliográficos
Autores principales: Egger, Melissa, Koehne, Ingo, Wickenhauser, Dominik, Schlemmer, Werner, Spirk, Stefan, Pietschnig, Rudolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061590/
https://www.ncbi.nlm.nih.gov/pubmed/37008129
http://dx.doi.org/10.1021/acsomega.2c07234
Descripción
Sumario:[Image: see text] Here, we investigate the electrochemical properties and stability of 1,1′-ferrocene-bisphosphonates in aqueous solutions. (31)P NMR spectroscopy enables to track decomposition at extreme pH conditions revealing partial disintegration of the ferrocene core in air and under an argon atmosphere. ESI-MS indicates the decomposition pathways to be different in aqueous H(3)PO(4), phosphate buffer, or NaOH solutions. Cyclovoltammetry exhibits completely reversible redox chemistry of the evaluated bisphosphonates, sodium 1,1′-ferrocene-bis(phosphonate) (3) and sodium 1,1′-ferrocene-bis(methylphosphonate) (8), from pH 1.2 to pH 13. Both the compounds feature freely diffusing species as determined using the Randles-Sevcik analysis. The activation barriers determined by rotating disk electrode measurements revealed asymmetry for oxidation and reduction. The compounds are tested in a hybrid flow battery using anthraquinone-2-sulfonate as the counterside, yielding only moderate performance.