Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1333422 | Journal of Solid State Chemistry | 2007 | 6 Pages |
The vanadium–molybdenum mixed oxide bronzes of composition K0.23(V5.35Mo0.65)O15 and K0.32(V5.48Mo0.52)O15 have a monoclinic structure with s.g. C2/m, Z=2, and unit-cell dimensions a=15.436(2), b=3.6527(5), c=10.150(1) Å, β=108.604(3)° and a=15.452(2), b=3.6502(5), c=10.142(1) Å, β=109.168(3)°, respectively, as determined by single-crystal X-ray diffraction. These compounds show the β-NaxV6O15 tunnel structure, which is isostructural with bannermanite, natural sodium–potassium vanadate. Structure refinements from diffracted intensities collected in the 2–38°θ range converged to final R=5.58% and 7.48% for the two crystals, respectively. The V atoms are distributed on three different crystallographic sites. Partial substitution of V with Mo occurs in only one of these positions. Oxygen atoms involved in vanadyl groups point toward the tunnels. The K ions in the tunnels are coordinated by seven oxygen atoms. The alkali metal content in these crystals is much lower than the solubility limit found for the analogous Na containing compound.
Graphical abstractPerspective view of the crystal structure of KxV6-yMoyO15 along [010].This vanadium–molybdenum mixed bronze assumes the β-NaxV6O15 (bannermanite-type) structure, in which Mo(VI) substitutes for V only in the V2 position. The alkali metal content in the studied crystals is much lower than the solubility limit found for the analogous Na containing compounds.Figure optionsDownload full-size imageDownload as PowerPoint slide