Crystal structures of two decavanadates(V) with pentaaquamanganese(II) pendant groups: (NMe4)2[V10O28{Mn(H2O)5}2]·5H2O and [NH3C(CH2OH)3]2[V10O28{Mn(H2O)5}2]·2H2O
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چکیده
Two heterometallic deca-vanadate(V) compounds, bis-(tetra-methyl-ammonium) deca-aquadi-μ4-oxido-tetra-μ3-oxido-hexa-deca-μ2-oxido-hexa-oxidodimang-anese(II)-deca-vanadate(V) penta-hydrate, (Me4N)2[V10O28{Mn(H2O)5}2]·5H2O, A, and bis-{[tris-(hy-droxy-meth-yl)meth-yl]ammonium} deca-aquadi-μ4-oxido-tetra-μ3-oxido-hexa-deca-μ2-oxido-hexa-oxidodimanganese(II)deca-vanadate(V) dihydrate, [NH3C(CH2OH)3]2[V10O28{Mn(H2O)5}2]·2H2O, B, have been synthesized under mild reaction conditions in an aqueous medium. Both polyanions present two [Mn(OH2)5](2+) complex units bound to the deca-vanadate cluster through oxide bridges. In A, the deca-vanadate unit has 2/m symmetry, whereas in B it has twofold symmetry. Apart from this, the main differences between A and B rest on the organic cations, tetra-methyl-ammonium and [tris-(hy-droxy-meth-yl)meth-yl]ammonium, respectively, and on the number and arrangement of the water mol-ecules of crystallization. In both compounds, the H atoms from the coordinating water mol-ecules participate in extensive three-dimensional hydrogen-bonding networks, which link the cluster units both directly and through solvent mol-ecules and, in B, through the 'tris-' cation hydroxyl groups. The cation in B also participates in N-H⋯O hydrogen bonds. A number of C-H⋯O inter-actions are also observed in both structures.
منابع مشابه
Synthesis and characterization of materials containing arrays of decavanadate clusters.
The synthesis and characterization by single crystal x-ray structure analysis, manganometric titration, valence sum calculations, thermogravimetric analysis, and IR spectroscopic studies of (HN(CH2CH2)3NH)2(Na(H2O)2)(HV10O28)*2H2O (1) and (H3N-4-C5H4N)2(NH4)4(V10O28)*xH2O (2) has been described. The structure of 1 consists of alternating layers composed of two-dimensional arrays of decavanadate...
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