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      Bare magnetic nanoparticles: sustainable synthesis and applications in catalytic organic transformations

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          Abstract

          Naked magnetic nanoparticles are successfully used as magnetically recoverable catalysts for organic transformations; this review highlights recent progress in this rapidly growing field.

          Magnetic nanoparticles have become increasingly attractive in the field of catalysis over the last decade as they combine interesting reactivity with an easy, economical and environmentally benign mode of recovery. Early strategies focused on the use of such nanoparticles as a vehicle for supporting other catalytic nanomaterials or molecules to facilitate recovery. More recently, research has shown that bare magnetic nanoparticles may serve the dual role of a catalyst and a magnetically recoverable entity. At the same time, emerging sustainability concepts emphasize the utility of earth abundant and less toxic resources, especially iron. Herein, we review the recent progress made in the assembly of such systems and their direct application in catalysis. Examples of such bare nanoparticles include iron oxide (Fe 2O 3 and Fe 3O 4), metal ferrites (MFe 2O 4, M = Cu, Co and Ni), Fe(0), Co(0), Ni(0), and multi-component nanoparticles. Features such as reactivity, recoverability and leaching are discussed in a critical fashion.

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          Nanoparticles as recyclable catalysts: the frontier between homogeneous and heterogeneous catalysis.

          Interest in catalysis by metal nanoparticles (NPs) is increasing dramatically, as reflected by the large number of publications in the last five years. This field, "semi-heterogeneous catalysis", is at the frontier between homogeneous and heterogeneous catalysis, and progress has been made in the efficiency and selectivity of reactions and recovery and recyclability of the catalytic materials. Usually NP catalysts are prepared from a metal salt, a reducing agent, and a stabilizer and are supported on an oxide, charcoal, or a zeolite. Besides the polymers and oxides that used to be employed as standard, innovative stabilizers, media, and supports have appeared, such as dendrimers, specific ligands, ionic liquids, surfactants, membranes, carbon nanotubes, and a variety of oxides. Ligand-free procedures have provided remarkable results with extremely low metal loading. The Review presents the recent developments and the use of NP catalysis in organic synthesis, for example, in hydrogenation and C--C coupling reactions, and the heterogeneous oxidation of CO on gold NPs.
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            Magnetically recoverable nanocatalysts.

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              Synthesis of highly crystalline and monodisperse maghemite nanocrystallites without a size-selection process.

              The synthesis of highly crystalline and monodisperse gamma-Fe(2)O(3) nanocrystallites is reported. High-temperature (300 degrees C) aging of iron-oleic acid metal complex, which was prepared by the thermal decomposition of iron pentacarbonyl in the presence of oleic acid at 100 degrees C, was found to generate monodisperse iron nanoparticles. The resulting iron nanoparticles were transformed to monodisperse gamma-Fe(2)O(3) nanocrystallites by controlled oxidation by using trimethylamine oxide as a mild oxidant. Particle size can be varied from 4 to 16 nm by controlling the experimental parameters. Transmission electron microscopic images of the particles showed 2-dimensional and 3-dimensional assembly of particles, demonstrating the uniformity of these nanoparticles. Electron diffraction, X-ray diffraction, and high-resolution transmission electron microscopic (TEM) images of the nanoparticles showed the highly crystalline nature of the gamma-Fe(2)O(3) structures. Monodisperse gamma-Fe(2)O(3) nanocrystallites with a particle size of 13 nm also can be generated from the direct oxidation of iron pentacarbonyl in the presence of oleic acid with trimethylamine oxide as an oxidant.
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                Author and article information

                Journal
                GRCHFJ
                Green Chem.
                Green Chem.
                Royal Society of Chemistry (RSC)
                1463-9262
                1463-9270
                2014
                2014
                : 16
                : 10
                : 4493-4505
                Article
                10.1039/C4GC00418C
                a976609f-ef6e-4784-bc28-10256508f083
                © 2014
                History

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