The complexation of phosphate ion by beta-amino-cyclodextrin (host 1)
was detected by voltammetric methods through the competitive displacem
ent of water-soluble ferrocene derivatives from their complexes with h
ost 1 in neutral aqueous media. The half-wave potential and the anodic
peak current for oxidation of the ferrocene derivative were found to
be sensitive to the phosphate concentration throughout a range which i
s determined, among other factors, by the concentration of host 1 and
the binding constant between the selected ferrocene derivative and the
beta-amino-cyclodextrin host.