P. Zanello et al., REDOX BEHAVIOR OF FERROCENE DERIVATIVES .8. 1,1'-BIS(DIPHENYLPHOSPHINO) FERROCENES, Journal of organometallic chemistry, 506(1-2), 1996, pp. 61-65
A study has been made of the possibility of increasing the stability o
f the 1,1'-bis(diphenylphosphino)ferrocenium monocation by introductio
n of appropriate substituents into the cyclopentadienyl ligands. The e
lectrochemical behaviour of a series of 1,1-bis(diphenylphosphino)ferr
ocenes bearing substituents with a range of electronic properties has
been examined. The results reveal that, the higher the electron-donati
ng ability of the substituents, the longer is the lifetime of the corr
esponding 1,1'-bis(diphenylphosphino)ferrocenium monocation. However,
no stable ferrocenium cation has been obtained; mass spectrometry show
s that mixtures of mono- and di-bis(diphenylphosphine)oxides are ultim
ately formed as products resulting from decomposition of the initially
electrogenerated 1,1'-bis(diphenylphosphino)ferrocenium species.