Sequestering uranium from seawater: binding strength and modes of uranyl complexes with glutarimidedioxime

Glutarimidedioxime (H(2)A), a cyclic imide dioxime ligand that has implications in sequestering uranium from seawater, forms strong tridentate complexes with UO(2)(2+). The stability constants and the enthalpies of complexation for five U(vi) complexes were measured by potentiometry and microcalorimetry. The crystal structure of the 1?:?2 metal-ligand complex, UO(2)(HA)(2)·H(2)O, was determined. The re-arrangement of the protons of the oxime groups (-CHdouble bond, length as m-dash]N-OH) and the deprotonation of the imide group (-CH-NH-CH-) results in a conjugated system with delocalized electron density on the ligand (-O-N-C-N-C-N-O-) that coordinates to UO(2)(2+)via its equatorial plane.