Add time:08/15/2019         Source:sciencedirect.com

Recent progress in carbon–carbon cross-coupling reactions has resulted in the discovery of highly active catalysts for carrying out such transformations. However, due to the wide array of applications of the products from cross-coupling reactions, there is the need to design suitable catalysts that permit the practical and economical synthesis of the cross-coupled products. Palladium complexes with bulky and electron-donating ligands have served as excellent (pre)catalysts for the Mizoroki–Heck cross-coupling reaction. By using bulky pyrazole-based ligands, we have prepared palladium(II) complexes with controlled steric and electronic properties of the metal center. We have used these bulky bis(pyrazolyl)palladium(II) complexes as (pre)catalysts for the Mizoroki–Heck cross-coupling reaction. The (pre)catalysts displayed high activity and selectivity, giving high catalytic conversions at a low (pre)catalyst loading and short reaction times. A mercury poisoning test confirmed that the (pre)catalysts promoted the Mizoroki–Heck cross-coupling homogenously and do not decompose into palladium black during the reactions. The catalytic systems were also tolerant to the presence of functional groups, such as 4-CF3, 4-CH3, 4-CO2Me and 4-CO2Et, on the alkene substrates.

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