Oxidation chemistry of uranium(III) complexes of Tpa: synthesis and structural studies of oxo,hydroxo, and alkoxo complexes of uranium(IV)

The crystal structure of the complex U(tpa)(2)]I(3), 1 (tpa = tris(2-pyridyl)methyl]amine), has been elucidated. The complex exists as only one enantiomer in the crystal leading to the chiral space group P2(1)2(1)2(1). The coordination geometry of the metal can be described as a distorted cube. Accidental oxidation of U(tpa)(2)]I(3) led to the isolation of the unusual mononuclear bishydroxo complex of uranium(IV) U(tpa)(2)(OH)(2)]I(2).3CH(3)CN, 2, which was structurally characterized. The controlled reaction of U(tpa)(2)]I(3) with water resulted in the oxidation of the metal center and led to the formation of protonated tpa and of the trinuclear U(IV) oxo complex (U(tpa)(mu-O)I](3)(mu(3)-I))I(2), 3. The solid state and solution structures of this trimer are reported. The pathway suggested for the formation of this complex is the oxidation of the U(tpa)(2)]I(3) complex by H(2)O to form a U(IV) hydroxo complex which then decomposes, eliminating mono-protonated tpa. The comparison with the reported reaction with water of cyclopentadienyl derivatives points to a higher reactivity toward water reduction of the bis(tpa) complex with respect to the cyclopentadienyl derivatives. The reaction of U(III) with methanol in the presence of the supporting ligand tpa leads to formation of alkoxo complexes similarly to what is found for amide or cyclopentadienyl derivatives. The monomethoxide complex U(tpa)I(3)(OMe)], 4, has been prepared in good yield by alcoholysis of the U(III) mono(tpa) complex. The crystal structure of this complex has been determined. The reaction of U(tpa)(2)]I(3) with 2 equiv of methanol in acetonitrile allows the isolation of the bismethoxo complex of U(IV) U(tpa)I(2)(OMe)(2)], 5, in 35-47% yield, which has been fully characterized. To account for the oxidation of U(III) to U(IV) the suggested mechanism assumes that hydrogen is evolved in both reactions.