Abstract
The Sonogashira cross coupling reaction is an applied method for preparation of diarylethyne compounds from readily available aryl halide derivatives and phenyl acetylene. The coupling reaction using nickel complex of N,N′-Bis(2-hydroxyethyl)ethylenediamine onto core shell graphene oxide (GO@SiO2-BHED-Ni) as a catalyst was studied in this research. This heterogonous catalyst showed good thermal stability, highly efficiency and recyclability in the reaction. Moreover, the catalyst is simply separated and can be reused several times without significant loss of catalytic activity. A wide range of aryl halides was coupled successfully under palladium and phosphine free conditions. The use of this catalyst led to the formation of substituted aromatic alkynes in excellent yields and short reaction times.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.