
%0 Journal Article
%A Baker, AT 
%A Goodwin, HA 
%A Rae, AD 
%T Nickel(II) and iron(II) complexes of 4-(Pyridin-2-yl)thiazole: Spectral, magnetic and structural studies
%J Australian Journal of Chemistry
%D 1984/12/01
%V 37
%N 12
%P 2431-2440
%K 
%R https://doi.org/10.1071/CH9842431
%U https://www.publish.csiro.au/paper/CH9842431 
%X Iron(II) and nickel(II) complexes of 4-(pyridin-2-yl)thiazole (L) have been prepared. The electronic spectrum of [NiL3] [ClO2,]2 is similar to that of the corresponding complex of 2,2'-bipyridine (bpy) but indicates that the thiazole provides the weaker field, the actual value of Dq(Ni2+) being within the range which suggests the likely appearance of a spin transition in iron(III). The iron(II) complexes [FeL3] X2 (X = ClO4, BF4) are, however, low-spin both in the solid state and in solution. The structure of [NiL3] [ClO4]2.3H2O has been determined, and this reveals a close similarity in the coordination environment to that in [Ni(bpy),] SO4.7.5H2O. The compound is monoclinic, space group P21/c, with four molecules in a unit cell of dimensions a 9.404(4), b 29.169(8), c 17.900(8)Åº, &#946; 137.76(1)º. The disordered structure was refined to a residual R 0.087 for 2307 observed reflections. The pseudo-symmetric ligands are orientationally disordered and one anion was also disordered. Restrained refinement with 194 parameters for 85 atomic positions produced a reliable geometry. The ligands function as bidentates, giving the cation a distorted octahedral structure. 
