Abstract
Crystal and molecular structures of adducts of uranyl pivaloyltrifluoroacetonate with hexamethylphosphoramide [UO2(PTFA)2(HMPA)] (I) and of uranyl trifluoroacetylacetonate with trimethyl phosphate [UO2(TFA)2(TMP)] (II) were determined. Compound I crystallizes in the monoclinic system, space group P21/n; a = 16.9384(3), b = 9.1090(2), c = 20.9844(4) Å, β = 101.5337(10)°, V = 3172.34(11) Å3 (at 100 K); Z = 4. Compound II crystallizes in the rhombic system, space group Pbca; a = 17.8214(4), b = 7.7786(2), c = 30.9176(7) Å, V = 4285.97(18) Å3 (at 100 K); Z = 8. In both cases, the cis isomer in which the neutral ligand is located between the trifluoromethyl groups is realized. Compound I differing from II by the stronger branching of ligand periphery is characterized by stronger structural deformations in the crystal.
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Original Russian Text © G.V. Sidorenko, M.S. Grigor’ev, V.V. Gurzhiy, S.V. Krivovichev, D.N. Suglobov, 2009, published in Radiokhimiya, 2009, Vol. 51, No. 6, pp. 495–502.
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Sidorenko, G.V., Grigor’ev, M.S., Gurzhiy, V.V. et al. Crystal and molecular structure of adducts of uranyl pivaloyltrifluoroacetonate with hexamethylphosphoramide and of uranyl trifluoroacetylacetonate with trimethyl phosphate. Radiochemistry 51, 567–575 (2009). https://doi.org/10.1134/S1066362209060034
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DOI: https://doi.org/10.1134/S1066362209060034