Spectrum–structure correlation for visible absorption spectra of copper(II) complexes showing axial co-ordination in aqueous solution

We attempted to draw some general considerations regarding the ability of the visible absorption spectra to provide information on axial co-ordination around copper(II) ion in aqueous solution. A series of visible spectra was recorded on the copper(II)–2,2′-bipyridine and copper(II)–l-aspartic acid systems. 2,2′-Bipyridine is known for its ability to co-ordinate copper(II) in axial position(s) as well, while l-aspartic acid is a potential tridentate ligand whose ability to chelate in axial position has been here investigated.Combined pH-metric and visible absorption spectrophotometric measurements were performed: visible absorption spectra were recorded during alkalimetric titrations as a function of pH. Further computer-assisted treatment allowed obtaining absorption spectra of single complexes. A series of axially co-ordinated copper(II) complexes found in the literature was also considered. Structural assignment of planar complexes is based on an empirical equation previously published by our research group, which allows an estimation of the ligand field strength of the equatorial donor groups involved. This equation can now help to strengthen the discussion and to assess a criterion to establish the axial co-ordination mode of copper(II) ion. The location of a donor group along the z-axis of the copper(II) distorted octahedron causes a red shift in the absorption spectrum. A quantitative estimation of the red shift per donor group was performed and ranges of red shifts for single donor groups were identified: we calculated a mean value of 36 nm, while extreme values are 19 and 58 nm.

Structure proposed for the complexes: (a) Cu(bipy); (b) Cu(bipy)2; and (c) Cu(bipy)3. The ligand is schematised for sake of simplicity.Figure optionsDownload as PowerPoint slide