Ligand field stabilization energies complexes

Table 17.4 Ligand field stabilization energies for Mn304, Fe304 and Co304. Values for high-spin complexes in all cases except for octahedral Co ...

The graph shows what has become known as the "double-humped" appearance that reflects the fact that the ligand field stabilization energy for the aqua complexes begins at 0, increases to 12 Dq, then drops to 0 on going from d° to d5 and repeats the trend on going from d6 to d10 (see Table 17.4). 

Determine the ligand field stabilization energy for d°-d10 ions in tetrahedral complexes. Although there are no low-spin tetrahedral complexes, assume that there are. 

It has already been stated that chromium complexes of tridentate metallizable azo compounds occupy their position as the single most important class of metal complex dyestuffs because of their high stability. It should be noted, however, that in this context the term stability is not used in the thermodynamic sense but relates to the kinetic inertness of the complexes.25 Octahedral chromium(III) complexes have a tP electronic configuration and the ligand field stabilization energy associated with this is high.26 Ligand replacement reactions involve either a dissociative... 

Another manifestation of ligand field stabilization energy can be seen from the heats of hydration of the transition metal ions. For example, the hydration of a gaseous ion results in the formation of an aqua complex as represented by the equation... 

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