Synthesis and characterization of tri-titanium(iv)-1,2,3-substituted α-Keggin polyoxotungstates with heteroatoms P and Si. Crystal structure of the dimeric, Ti–O–Ti bridged anhydride form K10H2[α,α-P2W18Ti6O77]·17H2O and confirmation of dimeric forms in aqueous solution by ultracentrifugation molecular weight measurements†

Kenji Nomiya, Mizuto Takahashi, Katsunori Ohsawa, Jason A. Widegren

Journal of the Chemical Society Dalton Transactions · 2001 · 54 citations · 27 references

Concepts

Abstract

The preparation and characterization of the α-Keggin-type, novel tri-TiIV-1,2,3-substituted polyoxotungstates with heteroatoms P and Si are described. The molecular structure of K10H2[α,α-P2W18Ti6O77]·17H2O 1, obtained as a main product (30.4% yield) from the 1 ∶ 3 molar ratio reaction of tri-lacunary precursor Na9[A-PW9O34]·19H2O with Ti(SO4)2·4H2O in aqueous solution, was determined by X-ray structure analysis. It had the dimeric, anhydride structure formed by three Ti–O–Ti bonds linking two Keggin [α-1,2,3-PW9Ti3O40]9− units. From the filtrate after 1 was filtered off, a different compound 2 was obtained as a minor product. A related α-Keggin tri-TiIV-1,2,3-substituted polyoxotungstate with heteroatom Si, the dimeric anhydride form K10H4[α,α-Si2W18Ti6O77]·15H2O 3, was obtained as a main product (31.1% yield) from a 1 ∶ 3 molar ratio reaction of Na10[A-α-SiW9O34]·15H2O with Ti(SO4)2. Ultracentrifugation molecular weight measurements under less acidic conditions revealed that 1 and 3 were present as dimers in aqueous solution. Characterization of 1 and 3 was also accomplished by complete elemental analyses, TG/DTA, FTIR and solution (31P and 183W) NMR spectroscopies.

References

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