Three hexafluoridoiridates(IV), Ca[IrF<sub>6</sub>]·2H<sub>2</sub>O, Sr[IrF<sub>6</sub>]·2H<sub>2</sub>O and Ba[IrF<sub>6</sub>]
作者:Anton I. Smolentsev、Alexander I. Gubanov、Andrey M. Danilenko
DOI:10.1107/s0108270107044046
日期:2007.11.15
The structures of the hexafluoridoiridates(IV) of calcium, Ca[IrF6]center dot 2H(2)O [calcium hexafluoridoiridate(IV) dihydrate], strontium, Sr[IrF6]center dot 2H(2)O [strontium hexafluoridoiridate( IV) dihydrate], and barium, Ba[IrF6] [barium hexafluoridoiridate(IV)], have been determined by single-crystal X-ray analysis. The first two compounds are isomorphous. Their metal cations are eight-coordinated in a distorted square-antiprismatic coordination environment, and their anions are represented by an almost ideal octahedron. These two structures can be described as frameworks in which all atoms occupy general positions. Sr[RhF6] and Ba[ RhF6] have a different space group (R (3) over barm, from powder diffraction data) but similar cell dimensions. The structures are very close to that of Ba[IrF6]. The cation is in a cuboctahedral coordination. The metal atoms are located on special positions of (3) over bar symmetry, while the F atoms are in general positions.