Direct synthesis of anhydrous alkali-metal tetrafluorodioxouranates(VI), A2[UO2F4], and the first synthesis of alkali-metal diaquatetrafluorodioxouranate(VI) monohydrates, A2[UO2F4(H2O)2]·H2O (A = Na, K or NH4)

Bhattacharjee, Manish ; Chaudhuri, Mihir. K. ; Mandal, Gagan C. ; Srinivas, Pendyala (1994) Direct synthesis of anhydrous alkali-metal tetrafluorodioxouranates(VI), A2[UO2F4], and the first synthesis of alkali-metal diaquatetrafluorodioxouranate(VI) monohydrates, A2[UO2F4(H2O)2]·H2O (A = Na, K or NH4) J. Chem. Soc., Dalton Trans. (18). pp. 2693-2695. ISSN 0300-9246

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Official URL: http://doi.org/10.1039/DT9940002693

Related URL: http://dx.doi.org/10.1039/DT9940002693

Abstract

Anhydrous alkali-metal tetrafluorodioxouranates(VI), A2[UO2F4](A = Na, K or NH4), have been synthesised directly from the reaction of [UO2(O2)]·2H2O with aqueous HF and alkali-metal fluorides AF (A = Na, K or NH4). The yellow product obtained by addition of an alkali to an aqueous solution of [UO2(NO3)2]·6H2O yielded, with aqueous HF and alkali-metal carbonates, the alkali-metal diaquatetrafluorodioxouranate(VI) monohydrates, A2[UO2F4(H2O)2]·H2O (A = Na, K or NH4). The compounds are crystalline. Infrared and laser Raman spectroscopic investigations provided the basis of their structural assessment. The solution electrical conductance (ca. 242 Ω–1 cm2 mol–1) attests to their 2 : 1 ionic nature and stability in aqueous solution. Pyrolysis of [NH4]2[UO2F4(H2O)2]·H2O at 120 °C followed by deuteriation and IR spectroscopy of the product provided evidence for the occurrence of a molecule of lattice water and two aqua ligands.

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