Structural and Electronic Properties of Old and New A2[M(pinF)2] Complexes

Seven new homoleptic complexes of the form A(2)[M(pin(F))(2)] have been synthesized with the dodecafluoropinacolate (pin(F))(2-) ligand, namely (Me4N)(2)[Fe(pin(F))(2)], 1; (Me4N)(2)[Co(pin(F))(2)], 2; ((Bu4N)-Bu-n)(2)[Co(pin(F))(2)], 3; {K-(DME)(2)}(2)[Ni(pin(F))(2)], 4; (Me4N)(2)[Ni(pin(F))(2)], 5; {K-(DME)(2)}(2)[Cu(pin(F))(2)], 7; and (Me4N)(2)[Cu(pin(F))(2)], 8. In addition, the previously reported complexes K-2[Cu(pin(F))(2)], 6, and K-2[Zn(pin(F))(2)], 9, are characterized in much greater detail in this work. These nine compounds have been characterized by UV-vis spectroscopy, cyclic voltammetry, elemental analysis, and for paramagnetic compounds, Evans method magnetic susceptibility. Single-crystal X-ray crystallographic data were obtained for all complexes except S. The crystallographic data show a square-planar geometry about the metal center in all Fe (1), Ni (4), and Cu (6, 7, 8) complexes independent of countercation. The Co species exhibit square-planar (3) or distorted square-planar geometries (2), and the Zn species (9) is tetrahedral. No evidence for solvent binding to any Cu or Zn complex was observed. Solvent binding in Ni can be tuned by the countercation, whereas in Co only strongly donating Lewis solvents bind independent of the countercation. Indirect evidence (diffuse reflectance spectra and conductivity data) suggest that 5 is not a square-planar compound, unlike 4 or the literature K-2[Ni(pin(F))(2)]. Cyclic voltammetry studies reveal reversible redox couples for Ni(III)/Ni(II) in-5 and for Cu(III)/Cu(II) in 8 but quasi-reversible couples for the Fe(III)/Fe(II) couple in 1 and the Co(III)/Co(II) couple in 2. Perfluorination of the pinacolate ligand results in an increase in the central C-C bond length due to steric clashes between CF3 groups, relative to perhydropinacolate complexes. Both types of pinacolate complexes exhibit O-C-C-O torsion angles around 40 degrees. Together, these data demonstrate that perfluorination of the pinacolate ligand makes possible highly unusual and coordinatively unsaturated high-spin metal centers with ready thermodynamic access to rare oxidation states such as Ni(III) and Cu(III).