Synthesis, properties, and crystal structure of Cu3Mo8O23X2 (X = Cl, Br, I)

Citation
U. Steiner et al., Synthesis, properties, and crystal structure of Cu3Mo8O23X2 (X = Cl, Br, I), Z ANORG A C, 625(1), 1999, pp. 160-166
Citations number
18
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
ISSN journal
00442313 → ACNP
Volume
625
Issue
1
Year of publication
1999
Pages
160 - 166
Database
ISI
SICI code
0044-2313(199901)625:1<160:SPACSO>2.0.ZU;2-S
Abstract
Single crystals of the Cu3Mo8O23X2 compounds were grown by chemical transpo rt reactions at the lower temperature of a gradient 873-823 K without extra transport agent (auto transport). As DTA/TG measurements indicate, the gas eous compounds, necessary for chemical transport reactions, are formed by p artial decomposition of Cu3Mo8O23X2 at 873 K. Cu3Mo8O23Br2 crystallizes wit h the orthorombic space group Pbcm (a = 4.021(1), b = 22.978(2), c = 21.673 (2) Angstrom, Z = 4). The crystal structure consists of pentagonal columns (1)(infinity)[Mo6O7O20/2] linked by additional MoO6/2 octahedra. All the po lyhedra(pentagonal bipyramide, octahedra) are distorted. Infinite chains (1 )(infinity)[Cu3Br2] along [100] are arranged in tunnels with s-like square shape, left open by the pentagonal columns. Cu3Mo8O23Cl2 (a=4.010(1), b= 22 .942(2), c = 21.639(2) Angstrom) and Cu3Mo8O23I2 (a = 4.052(1), b = 23.075( 2), c = 21.719(2) Angstrom) are isotypic.