Metal-ligand distances for hexacoordinate complexes show a mutual inte
rrelation manifested in the fact that with increasing axial distances
the equatorial ones decrease and vice versa. These R(a) vs R(e) depend
ences have been registered for certain chromophores and also for hexaf
luoro, hexachloro, hexanitro and hexaaqua complexes. Based on the anha
rmonic shape of the adiabatic potential surface, a theoretical analysi
s yields the form of the R(a) vs R(e) dependence which, in the most si
mple form, is a hyperbolic function.