
TY  - JOUR
A1  - Baker, AT 
A1  - Goodwin, HA 
A1  - Rae, AD 
T1  - Nickel(II) and iron(II) complexes of 4-(Pyridin-2-yl)thiazole: Spectral, magnetic and structural studies
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1984
VL  - 37
IS  - 12
SP  - 2431
EP  - 2440
KW  - 
UR  - https://doi.org/10.1071/CH9842431 
N2  - 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. 
ER  -

