Abstract

The structure of a new type of polyoxo cluster complex that contains thirteen uranium atoms, {U13}, is reported. The complex crystallized from methanol containing tetra-valent uranium (UIV) with a basic organic ligand, and was characterized as di-chloridoocta-cosa-μ2-methano-lato-octa-kis-(methano-lato)octa-μ4-oxido-trideca-uranium, [U13(CH3O)35.7Cl2.3O8] or [U13(μ4-Ooxo)8Cl x (MeO)38-x ] (x = 2.3, MeO = methoxide) (I), by single-crystal X-ray diffraction. The characterized {U13} polyoxo cluster complex (I) possesses a single cubic uranium polyhedron at the centre of the cluster core. To the best of our knowledge, this is the very first example of a polyoxo actinide complex that bears a single cubic polyhedron in its structure. The cubic polyhedron in I is well comparable in shape with those in bulk UO2. The U-O bonds in the cubic polyhedron of I are, however, significantly shorter than those not only in bulk UO2 but also in another analogue in the {U38} cluster. This shortening of U-O bonds, together with BVS calculations and the overall negative charge (2-) of I, suggests that the central uranium atom in I, which forms the single cubic coordination polyhedron, is presumably oxidized to the penta-valent state (UV) from the original tetra-valent state (UIV). Complex I is, hence, the first example of a polyoxo cluster possessing a single cubic coordination polyhedron of UV.

Highlights

  • The structure of a new type of polyoxo cluster complex that contains thirteen uranium atoms, {U13}, is reported

  • The complex crystallized from methanol containing tetravalent uranium (UIV) with a basic organic ligand, and was characterized as dichloridooctacosa-2-methanolato-octakis(methanolato)octa-4-oxido-tridecauranium, [U13(CH3O)35.7Cl2.3O8] or [U13(4-Ooxo)8Clx(MeO)38–x] (x = 2.3, MeO = methoxide) (I), by single-crystal X-ray diffraction

  • The cubic polyhedron in I is well comparable in shape with those in bulk UO2

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Summary

Chemical context

Hydrolysis is one of the most fundamental reactions in aqueous chemistry. The strong hydrolysis of highly charged metal cations (M+n) induces olation (to form hydroxobridging: M–OH–M) and oxolation (to form oxo-bridging: M–O–M), which eventually results in the formation of hydroxo/oxo-bridged oligomer and cluster complexes in an aqueous solution (Henry et al, 1992). The Ce—O distances (average: 2.35 A ) in the central cubic polyhedron of the {Ce13} cluster are well comparable with those in bulk CeO2 (2.34 A ) (Wyckoff, 1963) Given these facts, it is reasonable to consider that the oxidation state of the uranium ion in the single cubic polyhedron (i.e. U6) is higher than the original tetravalent state of UIV, strengthening (and thereby shortening) the U—O bonds. It is reasonable to consider that the oxidation state of the uranium ion in the single cubic polyhedron (i.e. U6) is higher than the original tetravalent state of UIV, strengthening (and thereby shortening) the U—O bonds This supports the BVS results suggesting a pentavalent state for uranium centre U6 (UV). Despite having the same nuclearity of thirteen, {Al13} and {U13} are not well comparable in terms of structure and coordination chemistry

Supramolecular features
Synthesis and crystallization
Refinement
Full Text
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