The syntheses of three ferrocenoyl peptides (Fc-GG-OEt (2), Fc-AA-OBzl (3),
Fc-LF-OMe (4)) including their full spectroscopic characterization is repo
rted. Titration of peptide solution with 3-aminopyrazole (APzl) in CDCl3 wa
s followed by H-1-NMR spectroscopy and evaluated using Job's method and by
non-linear regression. It was found that 4 showed the strongest interaction
with APzl, followed by 3. The highly flexible 2 showed only a weak interac
tion. Association constants, derived from NMR measurements, are in the rang
e of 9.4 +/- 1.0 to 21.4 +/- 0.5 M-1. Cyclic voltammetry shows that the red
ox potentials are sensitive to complex formation. The largest changes were
observed for 4 (30 mV), followed by 3 (13 mV) and there was no observable c
hange for 2. This sequence coincides with the ability of 3-APzl to form a c
omplex with the Fc-peptide. (C) 1999 Elsevier Science S.A. All rights reser
ved.