Kinetics and mechanisms of the electron-transfer reactions between uranium(III) and some ruthenium(III) ammine complexes

The rates of reduction of ) 7Ru(NH3)6{3+ and 7RuX(NH3)5{3+ (n = 2 or 3: X = H2O,OH-, Cl-,Br-, and 1-) by U3+ have been measured with a stopped-flow spectrophotometer. The reductions of 7Ru(NH3)6{3+ and 7Ru(NH3)(OH2){3+ proceed by an outer-sphere mechanism. The mechanism for 7Ru(NH3)5(OH){2+ is less certain, but is probably also outer sphere. The penta-amminehalogeno-complexes have a reactivity order I > Br> Cl, probably by an inner-sphere mechanism. The rates of reduction and reactivity patterns of equivalent cobalt(III) and ruthenium(III) complexes with a common reducing ion are compared. From the results, it is concluded that differences in the kinetic reactivity of the two metal complexes are due to the basic difference in the electronic structure of Cosup(III) and Rusup(III). These differences are manifested as influences of intrinsic factors on the rates and reactivity, and affect not only the rates of the reactions but also the type of mechanism often preferred. On the other hand, a comparison of rates of oxidation of U3+ with those of other aqua-ions employing Marcus theory leads to the conclusion that the very low reduction potential of U3+ is responsible for its very high redox reactivity. (author). )]