An 17O NMR Study of Hydrolyzed NbV in Weakly Acidic and Basic Aqueous Solutions

Time-dependent 17O NMR spectra of basified decaniobate (Nb10O286-) solutions displayed intense resonances assigned to the well-known protonated hexaniobate anion (Nb6O198-) and two other species identified as heptaniobate (Nb7O229-) and protonated tetracosaniobate (Nb24O7224-) anions. The decaniobate ion showed no sign of protonation from pH 6 - 10, in contrast with the hexaniobate ion which was protonated at doubly-bridging oxygen sites at pH 10-13. Most (> 90%) of the heptaniobate formed 1 h after basification was transformed into other species after 3 weeks. Tetracosaniobate was formed reversibly from decaniobate, but only when KOH, NaOH and (CH3)4NOH were employed; none was observed after basification with (n-C4H9)4NOH. Moreover, far more tetracosaniobate was formed from KOH than from (CH3)4NOH. This effect was attributed to a tetracosaniobate cation binding site that binds K+ more readily than (CH3)4N+ but is too small to accommodate (n-C4H9)4N+.