Abstract
A novel silica functionalized N-heterocyclic carbene palladium complex was found to be a very efficient and reusable catalyst in the Suzuki and Sonogashira coupling reactions. The synthesized catalyst was characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), N2 adsorption analysis (BET), thermal gravimetric analysis (TGA) and inductively coupled plasma/atomic emission spectroscopy (ICP/AES). The catalysts showed excellent performance in these two reactions including various aryl halide derivatives (except aryl chloride derivatives) with phenylboronic acid and phenylacetylene under green conditions (H2O). Moreover, the catalyst was recycled for several runs without any significant loss of catalytic activity.
Sign-in/Register to access full text options 
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 callDisclaimer: 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.
