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Crystals of the title compound, 2,5-di­methyl­piperazinediium β-octamolybdate, were grown under mild hydro­thermal conditions. The anion and cations lie on inversion centers. A network of N—H...O bonds helps to stabilize the crystal packing.

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The title compound, poly[N,N,N′,N′-tetra­methyl­propane-1,3-diaminium [aqua­tetra­oxotri-μ3-sulfatodiuranate(VI)]], (C7H20N2)[(UO2)2(SO4)3(H2O)]n, contains two-dimensional [(UO2)2(SO4)3(H2O)]2− layers that are unprecedented in uranium chemistry. The layers in this compound are separated by C7H20N22+ cations, forming the basis of an extensive hydrogen-bonding network. An independent intra­layer hydrogen-bonding network is also observed, involving water mol­ecules bound directly to a uranium centre.

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The title compound, bis­(propane-1,2-diaminium) tetra­aquadi-μ2-sulfato-disulfatotetra­oxodiuranate(VI) dihydrate, (C3H12N2)2[U2O4(SO4)4(H2O)4]·2H2O, contains discrete centrosymmetric anionic {[UO2(H2O)2(SO4)2]2}4− dimers with C3H12N22+ cations balancing the charge. The dimers form hydrogen-bonded layers. The cations and occluded water mol­ecules participate in an extensive hydrogen-bonding network. Each UVI centre is seven-coordinate with a penta­gonal–bipyramidal geometry. Both pendent and bridging sulfate tetra­hedra are observed, as well as bound and occluded water mol­ecules.

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Crystals of the title compound, 2-(dimethyl­ammonio)­ethanaminium hexa­cosa­oxaocta­molybdate(VI) dihydrate, containing extended chains constructed from centrosymmetric octa­molybdate anions, were grown under mild hydro­thermal conditions in the presence of N,N-dimethyl­ethylenediamine. An extensive hydrogen-bonding network helps stabilize the crystal structure.
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