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Mn 3 O 4 nanoparticles were synthesized via an ionic liquid (IL) assisted process at room temperature, which is rather difficult to achieve by other techniques. The synthesized product was characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, thermal gravimetry (TG), and vibrating sample magnetometry (VSM). The prepared material showed a high purity, while crystallite size and particle size agree well with each other, 17 ± 2 and 19 ± 3 nm, respectively, revealing nearly single crystalline character of nanoparticles. The product contains 4 wt% of adsorbed water and ionic liquid. This method provides a facile, one-step, and low-cost route for the synthesis of nanostructures of metal oxides. In addition, [BMIM]BF 4 could be collected and reused for subsequent reactions.

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In this present study, a facile synthetic route was developed to prepare super-paramagnetic Fe 3 O 4 MNPs directly via a one-pot approach. In this synthesis, only one iron containing compound and instead of high-boiling-point solvents, water-soluble tetraethylene glycol (TEG) was used as both the solvent and surfactant to control the particle growth and to prevent the aggregation of particles. Crystallite, particle, and magnetic core size are in good agreement with each other. The VSM measurement shows the superparamagnetic property of the product. The existence of TEG layer on the surface of the Fe 3 O 4 nanoparticles was confirmed by Fourier transform infrared spectroscopy and thermal gravimetric analysis. The monodisperse morphology of the product was presented via TEM analysis. Due to the monodisperse morphology, superparamagnetic property, and small particle size, the product may have a potential application in biomedical research field.