From iron coordination compounds to metal oxide nanoparticles

Various types, shapes and sizes of iron oxide nanoparticles were obtained depending on the nature of the precursor, preparation method and reaction conditions. The mixed valence trinuclear iron acetate, [Fe2 (FeO)-Fe-III-O-II(CH3COO)(6)(H2O)(3)]center dot 2H(2)O (FeAc1), mu(3)-oxo trinuclear iron(III) acetate, [Fe3O(CH3COO)(6)(H2O)3]NO3 center dot 4H(2)O (FeAc2), iron furoate, [Fe3O(C4H3OCOO)(6)(CH3OH)(3)]NO3 center dot 2CH(3)OH (FeF), iron chromium furoate, FeCr2O(C4H3OCOO)(6)(CH3OH)(3)] NO3 center dot 2CH(3)OH (FeCrF), and an iron complex with an original macromolecular ligand (FePAZ) were used as precursors for the corresponding oxide nanoparticles. Five series of nano-particle samples were prepared employing either a classical thermal pathway (i.e., thermal decomposition in solution, solvothermal method, dry thermal decomposition/calcination) or using a nonconventional energy source (i.e., microwave or ultrasonic treatment) to convert precursors into iron oxides. The resulting materials were structurally characterized by wide-angle X-ray diffraction and Fourier transform infrared, Raman, energy-dispersive X-ray, and X-ray fluorescence spectroscopies, as well as thermogravimetric analysis. The morphology was characterized by transmission electron microscopy, atomic force microscopy and dynamic light scattering. The parameters were varied within each route to fine tune the size and shape of the formed nanoparticles.