The development of ligands with high selectivity and affinity for uranium is critical in the extraction of uranium from human body, radioactive waste, and seawater. A scientific challenge is the improvement of the selectivity of chelators for uranium over other heavy metals, including iron and vanadium. Flat ligands with hard donor atoms that satisfy the geometric and electronic requirements of the (UO22+)-O-VI exhibit high selectivity for the uranyl moiety. The bis(hydroxylamino) (triazine) land, 2,6-bis[hydroxy(methypamino]-4-morpholino-1,3,5-triazine (H(2)bihyat), a strong binder for hard metal ions (Fe-II,Ti-V,V-V,V- and Mo-VI), reacted with [(UO2)-O-VI(NO3)(2)(H2O)center dot 4H(2)O in aqueous solution and resulted in the isolation of the complexes [(UO2)-O-VI(bihyat)(H2O)], [(UO2)-O-VI(bihyat)(2)](2-), and {[(UO2)-O-VI(bihyat)(mu-OH)]}(2)(2-). These three species are in equilibrium in aqueous solution, and their abundance varies with the concentration of H(2)bihyat and the pH. Reaction of H(2)bihyat with [(UO2)-O-VI(NO3)(2)(H2O)(2)]center dot 4H(2)O in CH3CN gave the trinuclear complex [(U3O6)-O-VI(bihyat)(2)(mu-bihyat)(2)](2-), which is the major species in organic solvents. The dynamics between the (UO22+)-O-VI and the free ligand H(2)bihyat in aqueous and dimethyl sulfoxide solutions; the metal binding ability of the H(2)bihyat over pyridine-2,6-dicarboxylic acid (H(2)dipic) or glutarimidedioxime for (UO22+)-O-VI, and the selectivity of the H(2)bihyat to bind (UO22+)-O-VI in comparison to (VO43-)-O-V and Fe-III in either (UO22+)-O-VI/(VO43-)-O-V or (UO22+/FeIII)-O-VI solutions were examined by NMR and UV vis spectroscopies. The results revealed that H(2)bihyat is a superior ligand for (UO22+)-O-VI with high selectivity compared to Fe-III and (VO43-)-O-v, which increases at higher pHs. Thus, this type of ligand might find applications in the extraction of uranium from the sea and its removal from the environment and the human body.