Synthesis, crystal structure and DFT analysis of a new trinuclear complex of copper

Abstract

The new trinuclear complex [Cu 2(μ-L) 2CuCl 2] has been synthesized and characterized by elemental analysis, IR, UV–Vis and X-ray spectroscopy, where L is a dianionic tetradentate Schiff base ligand with N 2O 2 donor atoms. The molecular structure of [Cu 2(μ-L) 2CuCl 2] was determined by X-ray crystallography. In the complex, the most remarkable aspect of the trinuclear complex is that it adopts a bent structure for the three copper atoms, with a Cu1 Cu3 Cu2 intramolecular angle of approximately 90.62(2)°. All three copper atoms are five coordinate, with a slightly distorted square pyramidal geometry. In the two terminals moieties, the basal plane of the square pyramidal is formed by two oxygen atoms and two nitrogen atoms of the Schiff base ligand, and the apical position at the Cu atom is occupied by the bridging Cl1 anion. The Cu1 Cl1 Cu2 angle is 110.51(5)°. The central copper atom also has a five-coordinate, slightly distorted square pyramidal geometry, with four phenolato oxygens belonging to the Schiff base ligands from Cu(salpn) units describing the square planar base and the Cl anions being apical. The optimized structure of the complex has been studied using the B3LYP/6-31G(d)/LanL2TZf level of theory. The calculation shows that all the copper atoms are five coordinate with distorted square pyramidal structures, which is consistent with experimental data.