Abstract
A novel highly efficient monodentate imine palladium catalyst system has been tested for Suzuki cross-coupling reaction. Under the standard conditions, a series of aryl halides, including phenyl iodide, aryl bromides and phenyl chloride, were coupled with phenylboronic or 1-naphthylboronic acid, producing the corresponding biaryls in good to excellent yields. High-resolution transmission electron microscopy (HR-TEM) study of the recycled catalyst showed the formation of palladium nano particles in the catalytic system.
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