Magnetic coupling in trinuclear partial cubane copper (II) complexes with a hydroxo bridging core and peripheral phenoxo bridges from NNO donor Schiff base ligands

Abstract

Three new trinuclear copper (II) complexes, [(CuL¹)₃(μ₃-OH)](ClO₄)₂•3.75H₂O (1), [(CuL₂)₃(μ ₃-OH)](ClO₄)₂ (2) and [(CuL³)₃(μ ₃-OH)](BF₄)₂•0.5CH₃CN (3) have been synthesized from three tridentate Schiff bases HL¹, HL² and HL³ (HL¹ = 2-[(2-amino-ethylimino)-methyl]-phenol, HL² = 2-[(2-methylamino-ethylimino)-methyl]-phenol and HL³ = 2-[1-(2-dimethylamino-ethylimino)-ethyl]-phenol). The complexes are characterized by single-crystal X-ray diffraction analyses, IR, UV–vis and EPR spectroscopy, and variable-temperature magnetic measurements. All the compounds contain a partial cubane [Cu₃O₄] core consisting of the trinuclear unit [(CuL) ₃(μ ₃-OH)]²⁺ together with perchlorate or fluoroborate anions. In each of the complexes, the three copper atoms are five-coordinated with a distorted square-pyramidal geometry except in complex 1, in which one of the Cu^II ions of the trinuclear unit is six-coordinate being in addition weakly coordinated to one of the perchlorate anions. Variable-temperature magnetic measurements and EPR spectra indicate an antiferromagnetic exchange coupling between the Cu^II ions of complexes 1 and 2, while this turned out to be ferromagnetic for complex 3. Experimental values have been fitted according to an isotropic exchange Hamiltonian. Calculations based on Density Functional Theory have also been performed in order to estimate the exchange coupling constants in these three complexes. Both sets of values indicate similar trends and specially calculated J values establish a magneto-structural correlation between them and the Cu–O–Cu bond angle, in that the coupling is more ferromagnetic for smaller bond angle values.