A series of Tris-(hydroxamate)-tri-aqua complexes of iron (Ill) with benzohydroxamic and nuclear substituted benzohydroxamic acid derivatives as ligands were investigated by Mtissbauer spectroscopy. The substitutions changed the electron density on the donor atoms of the legend moiety by their electrphelic and \ or nucleophelic nature and changed the symmetry of the complexes by their differential space requirements. Both the effects are reflected in the isomer shifts as well as the quadrupole splitting values.