TY - JOUR
T1 - Electrochemistry and Stability of 1,1′-Ferrocene-Bisphosphonates
AU - Egger, Melissa
AU - Koehne, Ingo
AU - Wickenhauser, Dominik
AU - Schlemmer, Werner
AU - Spirk, Stefan
AU - Pietschnig, Rudolf
N1 - Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society.
PY - 2023/3/28
Y1 - 2023/3/28
N2 - Here, we investigate the electrochemical properties and stability of 1,1′-ferrocene-bisphosphonates in aqueous solutions. 31P 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 H3PO4, 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.
AB - Here, we investigate the electrochemical properties and stability of 1,1′-ferrocene-bisphosphonates in aqueous solutions. 31P 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 H3PO4, 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.
UR - http://www.scopus.com/inward/record.url?scp=85149863036&partnerID=8YFLogxK
U2 - 10.1021/acsomega.2c07234
DO - 10.1021/acsomega.2c07234
M3 - Article
AN - SCOPUS:85149863036
SN - 2470-1343
VL - 8
SP - 10899
EP - 10905
JO - ACS Omega
JF - ACS Omega
IS - 12
ER -