The design and synthesis of acylhydrazone ligands and their corresponding metal complexes have received considerable attention 1 , as a result of which not only play important roles in the development of coordination chemistry related to magnetism 2 , enzymatic reactions 3 and pharmacological applications 4 , but also exhibit variety of biological activities 5. Schiff base ligands formed by reaction between the ovanillin group and benzoylhydrazine (3-methoxysalicylaldehyde benzoylhydrazide, hereafter abbreviated as H2L) is good candidates to construct metal clusters. The H2L has Oor N-donors and these donors with suitable relative positions in the ligand can coordinate to metal centers 6,7. Furthermore, the vanillin group displays a variety of bonding geometries, such as chelating, monodentate bridging, bidentate bridging and chelating bridging, although the coordination ability of the vanillin group is not strong in some cases 8,9. N-donor heterocycles can react with coordinatively unsaturated copper(II) complexes to give varieties of complexes where the heterocycles molecule is coordinated to the Cu(II) via the N-donor 10,11. Interestingly, the self-assembly patterns of the complexes having the general formula [Cu(L)(hc)] with other monodentate N-donor heterocycles (L = acylhy-drazone ligand, hc = pyrazole, imidazole or pyridine) are different 12,13. Herein, we reported two Cu(II) complexes, [Cu(HL)-(imidazole)]•ClO4 (1) and [Cu(HL)(pyrazol)]•ClO4 (2), using