B. Engelen et H. Muller, NEW POLYMORPHIC AND PSEUDOSYMMETRICAL COBALT SELENITE MONOHYDRATES, COSEO3-CENTER-DOT-H2O-II AND COSEO3-CENTER-DOT-H2O-III, Zeitschrift fur Kristallographie, 213(5), 1998, pp. 275-281
The crystal structures of two polymorphic, hydrothermally synthesized
cobalt selenite monohydrates, CoSeO3 . H2O II (a = 568.1(1) pm, b = 47
6.7(1) pm, c = 1348.0(2) pm, beta = 101.37(1)degrees) and CoSeO3 . H2O
III (a=477.2(1)pm, b = 1320.9(3)pm, c=568.6(1)pm, beta = 90.54(1)degr
ees), both mP32, P2(1)/n, Z = 4, have been determined by single crysta
l X-ray diffraction. Both structures are built up from buckled trans l
ayers (2)(infinity)[CoSeO3 . H2O] consisting of strongly distorted CoO
5(H2O) octahedra and trigonal pyramidal SeO32- ions. The structures di
ffer with respect to the stacking of the layers, which originates in t
heir pseudosymmetry and in the stereochemical requirements of the sele
nite lone electron pair. Only intra-layer H bond schemes are built, i.
e., the layers are held together by van der Waals interactions.