A bimetallic acetate-bridged (bis-2-pyridylidene)Pd(II) complex was synthesized and its oxidation behavior was investigated by cyclic voltammetry. The density functional theory calculation indicated that bis-2-pyridylidene is a potentially useful ligand to stabilize bimetallic Pd(III) species owing to its strong electron donation ability and high planarity. The di-tert-butylphenyl-substituted (bis-2-pyridylidene) Pd(II) carbonate complex was synthesized via sequential C-H borylation and Suzuki-Miyaura cross-coupling reactions, and the carbonate complex was successfully converted into an acetate-bridged bimetallic complex. The structural parameters and oxidation potentials of the acetate-bridged (bis-2-pyridylidene) Pd(II) complex indicated the strong electron donation ability of the bis-2-pyridylidene ligand compared with neutral bidentate ligands. Despite several attempts, (bis-2-pyridylidene) Pd(III) complexes could not be isolated because of their instability.