Abstract
An improved synthetic method of palladium(II) dinuclear macrocyclic complexes have been described. Each of the two isomers of the complexes [Pd 2LBr 2] has a macrocyclic ligand L in which two 2,6-bis(diaminomethyl)phenyl units coordinate to the Pd(II) centers with N, C, N donor atoms. Substitution of the bromo ligands of one of the isomer of the complexes with acetonitrile ligands affords a new dinuclear complex. Catalytic activities of these complexes were studied for the Mizoroki–Heck type reactions of iodobenzene and styrene. High turnover number up to 30,000 was achieved using one of the isomer of the complexes.
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