Effect of counterions and central cores of tripodal imidazolium salts on palladium-catalyzed Suzuki–Miyaura cross-coupling reactions

Abstract Seven tripodal imidazolium salts were synthesized and used as catalyst precursors in cross-coupling reactions of aryl halides with arylboronic acids. Effect of counterions and central cores of seven tripodal imidazolium salts was investigated. The tripodal imidazolium salt anchored to benzene with anion PF 6 − was found most effective with Pd(OAc) 2 for the cross-coupling of aryl bromides with arylboronic acids.