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September 5, 2025Australian Journal of Chemistry0 citations

One-electron oxidation and protonation of diferrocenylphenylphosphine

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CSCorina StoianSDSerhiy DemeshkoMFMalte Fischer

Key Points

  • The one-electron oxidation of diferrocenylphenylphosphine produces two stable cationic phosphorus species.
  • Spectroscopic techniques like UV-Vis, 31P NMR, and 57Fe Mößbauer spectroscopy reveal differences in the cations.
  • The structural similarity of the cations contrasts with their distinct electronic properties observed in various spectral analyses.
  • Bathochromic shifts in UV-Vis spectra indicate electronic changes associated with the radical cation.

Abstract

The one-electron oxidation and protonation of diferrocenylphenylphosphine (Fc2PhP) leads to the formation of two distinct, stable cationic phosphorus species, namely the radical cation Fc2PhPB(C6F5)4 and the phosphonium ion Fc2PhPHB(C6F5)4. Although their solid-state structures are remarkably similar, the bathochromic shift in the UV-Vis absorption spectrum of the radical cation, signals with distinct multiplicities in the 31P NMR spectra, as well as contrasting quadrupole splitting values in the 57Fe Mößbauer spectra, elucidated the differences between the two cations.

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Cite This Study

Stoian et al. (2025) studied this question.

synapsesocial.com/papers/68bb4df56d6d5674bcd0211ehttps://doi.org/10.1071/ch25087
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