The Solution Chemistry of Cu2+–tren Complexes Revisited: Exploring the Role of Species That Are Not Trigonal Bipyramidal

Authors

  • Carmen E. Castillo,

    1. Departamento de Ciencia de los Materiales e Ingeniería Metalúrgica y Química Inorgánica, Facultad de Ciencias, Universidad de Cádiz, Polígono Universitario Río San Pedro, Puerto Real, 11510 Cádiz, Spain
    2. Université Joseph Fourier Grenoble 1/CNRS, Département de Chimie Moléculaire, UMR-5250, Institut de Chimie Moleculaire de Grenoble FR-CNRS-2607, Laboratoire de Chimie Inorganique Redox, BP 53, 38041 Grenoble Cedex 9, France
    Search for more papers by this author
  • Andrés G. Algarra,

    1. Departamento de Ciencia de los Materiales e Ingeniería Metalúrgica y Química Inorgánica, Facultad de Ciencias, Universidad de Cádiz, Polígono Universitario Río San Pedro, Puerto Real, 11510 Cádiz, Spain
    Search for more papers by this author
  • M. Ángeles Máñez,

    1. Departamento de Ciencia de los Materiales e Ingeniería Metalúrgica y Química Inorgánica, Facultad de Ciencias, Universidad de Cádiz, Polígono Universitario Río San Pedro, Puerto Real, 11510 Cádiz, Spain
    Search for more papers by this author
  • Carole Duboc,

    1. Université Joseph Fourier Grenoble 1/CNRS, Département de Chimie Moléculaire, UMR-5250, Institut de Chimie Moleculaire de Grenoble FR-CNRS-2607, Laboratoire de Chimie Inorganique Redox, BP 53, 38041 Grenoble Cedex 9, France
    Search for more papers by this author
  • Manuel G. Basallote

    1. Departamento de Ciencia de los Materiales e Ingeniería Metalúrgica y Química Inorgánica, Facultad de Ciencias, Universidad de Cádiz, Polígono Universitario Río San Pedro, Puerto Real, 11510 Cádiz, Spain
    Search for more papers by this author

Abstract

Potentiometric and spectrophotometric titrations indicate that aqueous solutions that contain equimolar amounts of Cu2+ and tren contain the HCuL3+, CuL2+ and CuL(OH)+ species and that their relative concentrations depend on the pH of the solution. The stability constants and the UV/Vis and EPR spectra of the three species have been determined. The position of the absorption maximum clearly corresponds to a trigonal bipyramidal (tbp) geometry for CuL2+, whereas for HCuL3+ and CuL(OH)+ there are also bands that could correspond to square pyramidal (sp) complexes, but the EPR spectra indicate that only HCuL3+ can be considered to be sp. When any of these species is mixed with an excess of acid, an intermediate is formed within the mixing time of the stopped-flow technique. This intermediate undergoes complete decomposition in a second slower step. Interestingly, the spectrum of this intermediate is typical of sp geometry. Kinetic studies on complex formation in general indicate that complexation occurs in a single step, although under certain conditions an additional step has been observed that probably corresponds to the conversion of CuL2+ to HCuL3+, and the spectral changes indicate that the process involves structural reorganization from tbp to sp geometry. DFT and TD-DFT calculations have been carried out for the three stable species, as well as for species in a higher protonation state. The results indicate that CuL2+ exists as a species with tetradentate tren and tbp geometry, although a wide range of distortions between the ideal tbp geometry and a geometry closer to sp is possible with a very modest energy cost. The energy change associated with hydrolysis of one of the Cu–N bonds to give a species with tridentate tren was found to be slightly higher than that previously found for a related ligand, which contains a substituent at one of the terminal amino groups. For CuL(OH)+, the calculations suggest that an equilibrium exists between species with essentially the same energy but different geometries, each one of the species is closer to one of the ideal tbp and sp limits. For HCuL3+, the relevance of the sp geometry was confirmed by the calculations.

Ancillary