Two organically templated vanadium arsenate phases have been synthesiz
ed and characterized by single X-ray diffraction and thermogravimetric
analyses. Both are comprised of clusters of vanadium arsenate anions
that are held together by hydrogen bonding with the included species.
The V4As6O30H6 . 2 N2C6H14 . 4 H2O [VAs-Dab] (M(r) = 1439.76) crystal
is monoclinic, space group P2(1)/c (No. 14), with a = 9.247(3) angstro
m, b = 13.932(3) angstrom, c = 16.105(8) angstrom, beta = 106.31(4)-de
grees, V = 1991.26 angstrom3 and Z = 2. Final residuals of R = 3.71% a
nd R(w) = 4.17% were obtained for 3044 observed reflections with I > 3
sigma(I). The crystalline compounds is comprised of clusters H-bonded
to the organic and water molecules. The V4As6O30H8 . 2 N(CH3)4 . 5.33
H2O [VAsTMA] (M(r) = 346.43) crystal is orthorhombic, space group Cmca
(No. 64), with a = 18.742(5) angstrom, b = 12.208(3) angstrom, c = 17
.689(6) angstrom, V = 4047.24 angstrom3 and Z = 16. Final residuals of
R = 3.89% and R(w) = 4.13% were obtained for 1756 observed reflection
s with I > 3sigma(I). The crystalline compound contains one dimensiona
l channels, surrounded by the H-bonded clusters, containing the water
molecules and tetramethyl ammonium cations.