| Abstract: | Polyamidoamine (PAMAM) is one of the most interesting types of hyperbranched polymers that carry a large number of amino groups on its surface. PAMAM has gained significant attention from synthetic organic chemists due to its structural characteristics, controllable structure, inner porosity, and ability to trap a wide range of ions and molecules. So, in this work, the PAMAM dendrimer was synthesized, grafted onto the surface of magnetite nanoparticles, and the resulting hybrid nanoparticles were then employed as suitable host for immobilizing cobalt nanoparticles. The newly developed catalyst was well characterized by Fourier transform‐infrared, X‐ray diffraction, thermogravimetric analysis, field emission‐scanning electron microscopy, transmission electron microscopy, atomic absorption spectroscopy, element mapping and energy‐dispersive X‐ray analysis. The efficiency of the as‐prepared nanocatalyst was evaluated for the Mizoroki–Heck cross‐coupling reactions. The MNP@PAMAM‐Co represented perfect catalytic efficiency and high selectivity for the Mizoroki–Heck cross‐coupling reaction compared with previously reported catalysts. The catalyst separation from the reaction mixture was easily achieved with the assistance of an external magnetic field, and its recycling was also investigated for five consecutive runs. Hot filtration confirmed no leaching of the active metal during the Heck coupling. |
