Wta. Harrison et al., HYDROTHERMAL SYNTHESES AND CRYSTAL-STRUCTURES OF NEW LAYERED TUNGSTEN(VI) METHYLPHOSPHONATES, M(2)(WO3)(3)PO3CH3 (M=NH4, RB, CS), Journal of materials chemistry, 6(1), 1996, pp. 81-87
The hydrothermal syntheses of Cs-2(WO3)(3)PO3CH3, Rb-2(WO3)(3)PO3CH3 a
nd (NH4)(2)(WO3)(3)PO3CH3, three new noncentrosymmetric, layered tungs
ten(VI)-containing phases, are described. The crystal structures of Cs
-2(WO3)(3)PO3CH3 and (NH4)(2)(WO3)(3)PO3CH3 were refined by using Riet
veld analysis of powder diffraction data. These phases are built up fr
om hexagonal tungsten-oxide-libe layers of vertex-sharing WO6 groups,
capped by P-CH3 entities (as methylphosphonate groups) on one side of
the tungsten/oxide layer. Caesium, rubidium or ammonium cations provid
e interlayer charge compensation for the anionic layers. IR, Raman and
thermogravimetry (TG) data for these phases are also presented. Cryst
al data: Cs-2(WO3)(3)PO3CH3, M(r) = 1055.36, trigonal, space group R3
(no. 146), a = 7.25791(9) Angstrom, c = 20.2762(4) Angstrom, V = 925.0
0(4) Angstrom(3), Z = 3, R(p) = 2.37%, R(wp) = 3.12% (2943 neutron pow
der data). (NH4)(2)(WO3)(3)PO3CH3, M(r) = 825.63, trigonal, R3 (no. 14
6), a = 7.22851(7) Angstrom,c = 19.3471(3) Angstrom, V = 875.48(3) Ang
strom(3), Z = 3, R(p) = 8.14%, R(wp) = 10.12% (2665 X-ray powder data)
.