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Structure and Solution Speciation of UIV Linked Phosphomolybdate (MoV) Clusters
Author(s) -
Tapash Deb,
Lev N. Zakharov,
Clément Falaise,
May Nyman
Publication year - 2015
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.5b02229
Subject(s) - chemistry , aqueous solution , uranyl , polyoxometalate , inorganic chemistry , crystallography , dissolution , molybdate , sodium phosphates , uranium , actinide , sodium , ion , biochemistry , materials science , organic chemistry , metallurgy , catalysis
Crystals of [NaU(Mo6P4O31H7)2]·5Na·(H2O)n (NaUMo6) have been synthesized by slow evaporation of an aqueous mixture containing uranyl nitrate, sodium molybdate, phosphoric acid, and sodium dithionate. Single crystal diffraction of NaUMo6 reveals the assembly of {Mo6P4} clusters linked into one-dimensional chains with alternating Na(+) and U(4+) cations. To our knowledge, NaUMo6 is a unique example of Mo(5+) based polyoxometalate associated with actinides. With the use of similar synthesis conditions but without uranium in the aqueous solution, [Na(Mo6P4O31H10)2]·5Na·(H2PO4)·(H2O)n (NaMo6) is obtained. NaMo6 is a sandwich type cluster which is built on the assemblage of two {Mo6P4} units linked by one sodium cation. Using small-angle X-ray scattering techniques and aqueous electrolyte based dissolution strategies, we can accurately observe chains of [UNa(Mo6P4O31H7)2]n(5n), where n = 7 is the dominant soluble specie. Likewise, the dimeric form of [Na(Mo6P4O31H10)2](5-) dominates the aqueous solution, revealing the structural units observed in the crystal structure are also stable in solution, under appropriate dissolution conditions.

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