Abstract

The carbon–carbon cross coupling reactions through transition-metal-catalyzed processes has been significantly developed for their important synthetic applications. A novel and fantastic nickel-based catalyst supported on bis (propyl malononitrile) (NiFe2O4@SiO2-BPMN-Ni) was easily prepared and evaluated as heterogeneous nanocatalyst in Suzuki cross coupling reaction of various aryl halides and phenylboronic acid. The catalyst prepared and characterized by using fourier transform infrared (FT-IR), powder X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), thermo gravimetric analysis (TGA) and vibrating sample magnetometer (VSM) techniques. Compare to the previous works, this procedure have advantages such as easy workup, high yields of products, environmentally benign and short reaction times. The catalyst can be separated by external magnet and reused six times without any significant loss of activity which is an additional sustainable characteristic of this method. The products have been confirmed by spectroscopic and physical data such as; IR, 1H NMR, and melting point.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.