Uranyl peroxide capsules are a fascinating
class of polyoxometalates
(POMs), discovered only in the 21st century. Understanding the reactivity
between peroxide, alkali cations, and uranyl in alkaline solutions
is important in nuclear science disciplines including mineralogy,
nuclear energy, and legacy nuclear wastes. Here, we have developed
a general procedure to isolate different fragments of the uranyl-peroxide
POM capsules, using organic solvents to partially remove K+ salts from crude solids of the monomer building block UO2(O2)3
4– (K–U1
), leading to stabilization of these reactive fragments.
Higher polarity organic solvents remove more K+ salts from
the crude solid, owed to higher solubility, resulting in more extensive
linking of uranyl peroxide building units. By this strategy we have
isolated and structurally characterized a dimer K6[(UO2)2(O2)4(OH)2]·7H2O (K–U2
) and a hexamer face
frequently observed in the capsules, K12[(UO2)6(O2)9(OH)6]·xH2O (K–U6
). Comparing
experimental and computed Raman spectra shows that these intermediates
crystallize by a solid-to-solid transformation, via polymerization
of the monomer building block. By small-angle X-ray scattering (SAXS),
we track the conversion of the fragments to POM capsules; the reaction
rate increases from K–U1
(days) < K–U2
(hours) < K–U6
(instantaneous). This study provides a general synthetic
procedure to isolate metastable uranyl peroxide oligomers and control
the oligomerization, which will be later applied to systems with the
heavier alkalis that are even less stable.