The macrocyclic ligand of 3,6,9,16,19,22-hexaazatricyclo[22.2.2.2 1 1 , 1 4 ]-triaconta-1(26),11(12),13 ,24,27,29-hexaene(L, BP) was synthesized by [2+2] condensation of p-phthaldehyde and diethylenetriamine. This ligand was used to synthesize dicopper(II) complex [BPCu 2 (II)](ClO 4 ) 4 (1) and the bis-μ-X bridged tetracopper(II) complexes [BP 2 Cu 4 (II)(μ-X) 2 ] (X=Ph COO - (2), CO 3 2 - (3) and CH 3 O - (4)). Complex 3 crystallizes in the triclinic space group P1, with cell constants a=9.9965(10), b=13.5887(14), c=14.0262(7) Å, α=90.317(2), β=96.902(2), γ=92.691(2) o , V=1889.3(3) Å 3 and Z=2. Complexes 3 and 4 proved to be effective homogeneous catalysts for oxidative coupling of 2,6-dimethylphenol (DMP) to polyphenylene ether (PPE) by dioxygen. These complexes transform DMP to PPE under mild conditions of atmospheric pressure of O 2 and 298 K. The effectiveness of the catalytic reaction depends upon the type of the μ-X ligand and the concentration of the auxiliary NaOEt. Crystallographic and mechanistic investigation indicated that the catalytic center is the 'dimer-to-dimer' tetranuclear structure, and a novel mechanism for this polymerization reaction was proposed.