A series of novel ferrocene macrocyclic dioxopolyamines (1-4) hearing an im
inodiacetamide fragment in their framework were designed and synthesized, a
nd two such new ligands (2 and 4) and some of their complexes are reported.
The coordination behavior and electrochemical properties of these compound
s were systematically examined by cyclic voltammetry (CV) and electronic ab
sorption spectroscopy. Host-guest complexation stoichiometries (1:1) have b
een confirmed by fast atom bombardment mass spectroscopy (FAB MS) and UV-vi
s titration of cobalt ion and ligands 3 and 4. Additionally the stability c
onstants for the equilibrium of cobalt ion and ligands 3 and 4 have been ev
aluated. The coordination of the ligands with transition metal ions (Cu2+,
Ni2+ and Co2+) causes anodic shifts of the ferrocene redox couple to variou
s extents. The uncommon oxidation state of nickel(III) and copper(III) can
be selectively stabilized by tetra-azamacrocycle I and penta-azamacrocycles
, 3 and 4, respectively. (C) 2000 Elsevier Science S.A. All rights reserved
.