Abstract
Palladium nanoparticles supported on cross-linked polyaniline with bulky phosphorus ligands were developed. These catalysts showed high efficiency in the Suzuki-Miyaura reaction of aryl chlorides and bromides with phenylboronic acids. Aryl chlorides and bromides with functional groups, such as CN, MeO, CHO, MeCO and NO2, were converted to the corresponding biphenyls in high yields with catalyst loading. Additionally, the catalysts combined high activity with good reusability; they could be used at least five times for the Suzuki-Miyaura coupling reaction.
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