Synthesis, spectra and redox properties of mononuclear five-co-ordinate copper(II) complexes with non-communicable pyrazole pyridyl containing ligands - X-ray structure of [2,6-bis(3,5-dimethyl-pyrazol-1-ylmethyl)pyridine][2-(3,5-dimethylpyrazol-1-ylmethyl)pyridine]copper(II) diperchlorate

Synthesis and characterization of a series of five-co-ordinate mononuclear copper(II) compounds (1-8) have been achieved using tridentate/bidentate he terocyclic nitrogen donor ligands with mixed hard-soft donor sets [L-1 =2,6 -bis(pyrazol-1-ylmethyl)pyridine; L-2 =2,6-bis(3,5-dimethylpyrazol-1-ylmeth yl)pyridine; L-3=2-(pyrazol-1-ylmethyl)pyridine; L-4=2-(3,5-dimethylpyrazol -1-ylmethyl)pyridine]. Two types of complexes have been synthesized: (i) th e anion bound complexes [Cu(L-1/L-2)X-2] (X=Cl- land 2; N-3(-) 3 and 4; SCN - 5 and 6) and (ii) mixed-ligand complexes [Cu(L-1/L-2)(L-3/L-4)](ClO4)(2) 7 and 8. Complexes 1-8 belong to only a handful of copper(II) complexes wit h this class of non-planar ligands where pyrazole and pyridine rings are se parated by methylene spacer(s). A representative complex [Cu(L-2)(L-4)](ClO 4)(2) 8, having CuN5 co-ordination sphere, has been structurally characteri zed, to reveal square pyramidal stereochemistry at the copper(II) centre. C onductivity measurements revealed that one of the co-ordinated anions in 3, 5 and 6 is dissociated in solution, with the vacant site occupied by solve nt molecule. Absorption and EPR spectral features of 1-8 represent that the se copper(II) complexes adopt essentially a square pyramidal geometry. Howe ver, for 1 both in the solid state as well as in solution and for 2 in solu tion we propose that the copper(II) centre could be six-co-ordinate. Cyclic voltammetric measurements reveal the following trends in their E-1/2 value s (Cu-II-Cu-I redox process): (i) relative stabilization of Cu-II state by anionic ligands (N-3(-), Cl- or NCS-) and a strongly co-ordinating solvent like DMF and (ii) predominance of steric over electronic effect (L-1 vs. L- 2). (C) 1999 Elsevier Science Ltd. All rights reserved.