Xd. Wang et al., CRYSTAL-STRUCTURE AND RAMAN-SPECTROSCOPY OF FEVMOO7 AND CRVMOO7 WITH MO=0 DOUBLE-BONDS, Inorganic chemistry, 37(13), 1998, pp. 3252-3256
Single crystals of FeVMoO7 and CrVMoO7 were grown by a flux method fro
m Fe2O3-V2O5-MoO3 and Cr2O3-V2O5-MoO3 melts, respectively. Single-crys
tal X-ray diffraction revealed that FeVMoO7 and CrVMoO7 are isostructu
ral, in which V5+ and Mo6+ ions in the [VMoO7](3-) units are crystallo
graphically distinct, and one type of oxygen is bonded only to molybde
num, forming a Mo=O double bond. These rare structural features were a
lso studied by infrared and Raman spectroscopy. Raman Mo=O stretching
frequencies are consistent with the assignments made in previous surfa
ce studies of molybdate catalysts. Crystal data for FeVMoO7: triclinic
, space group P (1) over bar (No. 2), with a = 5.564(1) Angstrom, b =
6.669(1) Angstrom, c = 7.909(1) Angstrom, alpha = 97.65(1)degrees, bet
a = 90.33(1)degrees, gamma = 101.32(2)degrees and Z = 2. Crystal data
for CrVMoO7: triclinic, space group P (1) over bar (No. 2), with a = 5
.5273(9) Angstrom, b = 6.582(1) Angstrom, c = 7.8650(9) Angstrom, alph
a = 96.19(1)degrees, beta = 89.87(1)degrees, gamma = 102.01(1)degrees,
and Z = 2.