A highly sensitive and selective method is described for a rapid and easy d
etermination of iron(III). This procedure is based on fluorimetric detectio
n combined with the attractive properties of siderophores and biomimetic li
gands, which are strong and selective ferric chelators, Azotobactin delta,
a bacterial fluorescent siderophore, three fluorescent derivatives of desfe
rriferrioxamine B with a linear structure (NBD-, MA-, NCP-desferriferrioxam
ine B) and one tripodal biomimetic ligand of desferriferrichrome carrying a
n anthracenyl fluorescent probe were examined. A very efficient static quen
ching mechanism by iron was observed for all the ligands considered in this
work. Our results identify azotobactin delta as the most promising chemose
nsor of ferric traces in water, more sensitive than the NBD-desferriferriox
amine B fluorescent ligand. Under more lipophilic conditions, the anthryl-d
esferriferrichrome biomimetic analogue showed similar analytical potential
and was found to be more sensitive than the lipophilic MA- and NCP-desferri
ferrioxamine B. Their detection limits were respectively 0.5 ng mL(-1) for
azotobactin delta and 0.6 ng mL(-1) for the anthryl tripodal chelator. The
calibration curves were linear over the range 0-95 ng mL(-1) and 0-180 ng m
L(-1). Various foreign cations have been examined and only copper(II) and a
luminium(III) were shown to interfere when present in similar concentration
s as iron(III). The developed procedure using fluorescent siderophores or b
iomimetic ligands of iron(III) may be applied (1) to monitor iron(III)-depe
ndent biological systems and (2) to determine iron(III) quantitatively in n
atural waters and in biological systems.