Mechanistic insight on the reversible binding of NO to Fe-II chelate complexes as potential catalysts for the removal of NO from effluent gas streams has been obtained from the temperature and pressure parameters for the "on" and "off" reactions determined using a combination of flash photolysis and stopped-flow techniques. These parameters are correlated with those for water exchange reactions on the corresponding Fe-II and Fe-III chelate complexes, from which mechanistic conclusions are drawn. Small and positive DeltaAdouble dagger values are found for NO binding to and release from all the selected complexes, consistent with a dissociative interchange (I-d) mechanism. The only exception in the series of studied complexes is the binding of NO to [Fe-II(nta)(H2O)(2)](-). The negative volume of activation observed for this reaction supports the operation of an I-a ligand substitution mechanism. The apparent mechanistic differences can be accounted for in terms of the electronic and structural features of the studied complexes. The results indicate that the aminocarboxylate chelates affect the rate and overall equilibrium constants, as well as the nature of the substitution mechanism by which NO coordinates to the selected complexes. There is, however, no simple correlation between the rate and activation parameters and the selected donor groups or overall charge on the iron(II) complexes.