The solvation and electrochemical behavior of copper acetylacetonate complexes in ionic liquids

Abstract The behavior of copper(II) complexes of pentane-2,4-dione and 1,1,1,5,5,5-hexafluoro-2,4-pentanedione, [Cu(acac) 2 ] ( 1 ) and [Cu(HFacac) 2 (H 2 O)] ( 2 ), in ionic liquids and molecular organic solvents, was studied by spectroscopic and electrochemical techniques. The electron paramagnetic resonance characterization (EPR) showed well-resolved spectra in most solvents. In general the EPR spectra of [Cu(acac) 2 ] show higher g z values and lower hyperfine coupling constants, A z , in ionic liquids than in organic solvents, in agreement with longer Cu O bond lengths and higher electron charge in the copper ion in the ionic liquids, suggesting coordination of the ionic liquid anions. For [Cu(HFacac) 2 (H 2 O)] the opposite was observed suggesting that in ionic liquids there is no coordination of the anions and that the complex is tetrahedrically distorted. The redox properties of the Cu(II) complexes were investigated by cyclic voltammetry (CV) at a Pt electrode ( d  = 1 mm), in bmimBF 4 and bmimNTf 2 ionic liquids and, for comparative purposes, in neat organic solvents. The neutral copper(II) complexes undergo irreversible reductions to Cu(I) and Cu(0) species in both ILs and common organic solvents (CH 2 Cl 2 or acetonitrile), but, in ILs, they are usually more easier to reduce (less cathodic reduction potential) than in the organic solvents. Moreover, 1 and 2 are easier to reduce in bmimNTf 2 than in bmimBF 4 ionic liquid.