Dioxouranium(VI) complexes with 2,6-acetylpyridinebenzoylhydrazones and -semicarbazones

Abstract

Benzoylhydrazones and semicarbazones derived from 2,6-diacetylpyridine react with common dioxouranium(VI) compounds such as uranyl nitrate or [NBu 4] 2[UO 2Cl 4] to form air-stable complexes. 2,6-Diacetylpyridinebis(benzoylhydrazone) (H 2L 1), 2,6-diacetylpyridinebis(N4-phenylsemicarbazone) (H 2L 2) and the asymmetric proligand 2,6-diacetylpyridine(benzoylhydrazone)(N4-phenylsemicarbazone) (H 2L 3) give yellow products of the composition [UO 2(L)]. The neutral compounds contain doubly deprotonated ligands and possess uranium atoms with distorted pentagonal-bipyramidal coordination spheres. The equatorial coordination spheres of the metal atoms can be extended by the addition of a monodentate ligand such as pyridine or DMSO. The uranium atoms in the resulting complexes have hexagonal-bipyramidal coordination environments with the oxo ligands in axial positions. X-ray diffraction studies on [UO 2(L 1)(DMSO)], [UO 2(L 2)], [UO 2(L 2)(DMSO)] and [UO 2(L 3)] show relatively short U–O bonds to the benzoylic oxygen atoms between 2.273(6) and 2.368(5) Å. This suggests a preference of these donor sites of the ligands over their imino and amine functionalities (U–N bond lengths: 2.502(7)–2.671(7) Å). The addition of a sixth ligand to the equatorial coordination sphere results in a lengthening of the metal–pyridine bonds.