Poly[diammonium [diaqua(μ7-benzene-1,2,3,4,5,6-hexacarboxylato)tetraoxidodiuranium(VI)]]

• Main Authors: Paula M. Cantos, Christopher L. Cahill
• Format: Article
• Language: English
• Published: International Union of Crystallography 2014-04-01
• Series: Acta Crystallographica Section E
• Online Access: http://scripts.iucr.org/cgi-bin/paper?S1600536814006047

Uranyl-carboxylate hybrid materials dominate the catalog of uranyl compounds owing in part to the affinity between COO− functional groups and UO22+. Polycarboxylate organic ligands may present a degree of steric hindrance and could thus influence the resulting uranyl topology. Single crystals of the title compound, {(NH4)2[(UO2)2(C12O12)(H2O)2]}n, were synthesized hydrothermally as a result of reacting uranyl nitrate with benzene-1,2,3,4,5,6-hexacarboxylic acid (mellitic acid). The structure is comprised of a single unique monomeric uranyl cation adopting a pentagonal bipyramidal geometry. The uranyl coordination sphere is composed of four O atoms originating from one half of a fully deprotonated mellitic acid ligand and a single water molecule. The observed axial U—O bonds display an average distance of 1.765 (8) Å, whereas equatorial O atoms are found at an average distance of 2.40 (5) Å. All uranium–oxygen bond lengths are in good agreement with literature values. Furthermore, the coordination between the uranyl pentagonal bipyramids and the mellitic acid anion constructs a three-dimensional anionic framework which is charge-balanced with ammonium cations. Additional stabilization of the structure is provided by O—H...O and N—H...O hydrogen bonding interactions between the components.