There is a wide number of different synthetic methods to obtain magnetite (Fe3O4) superparamagnetic nanoparticles (SPNPs). However, only a few are able to produce very small and well defined SPNPs with narrow size distribution. We report a modification of the metal-complex decomposition in organic media method in which we replace iron(iii) acetylacetonate (Fe(Acac)3) with an iron–urea complex (Fe-Urea) as metal source for the synthesis. With this modification we were able to obtain small particle sizes with a good control in size distribution. The Fe-Urea complex is easy to prepare with excellent yields. Core–shell nanoparticles are then prepared using palladium(ii) acetylacetonate as a Pd source, to obtain a Pd0 shell stabilised by oleylamine. The core–shell superparamagnetic nanoparticles of Fe3O4@Pd-OA are extensively characterized by FT-IR, powder X-ray diffraction, transmission electron microscopy, UV-vis, thermogravimetric analysis/differential scanning calorimetry, and magnetic susceptibility measurements, and tested in a palladium-catalyzed cross-coupling Suzuki–Miyaura reaction with promising results.
The conductive properties of ink coating based on Ni–Ag core–shell nanoparticles with the bimodal size distribution
