The complex oxide Sr 11 Re 4 O 24 has been synthesized and its crystal structure was determined by a combination of X-ray powder analysis (space group I4 1 /a; aβ«Ψβ¬ 11.6779(1) A s , c β«Ψβ¬ 16.1488(2) A s ; Z β«Ψβ¬ 4) and electron di4raction. Re5nement of the crystal structure was carried out using neut
Preparation, Crystal Structure, and Magnetic Studies of a New Sr7Re4O19 Double Oxide and Its Relation to the Structure of Ba7Ir6O19
β Scribed by K.G. Bramnik; H. Ehrenberg; H. Fuess
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 390 KB
- Volume
- 160
- Category
- Article
- ISSN
- 0022-4596
No coin nor oath required. For personal study only.
β¦ Synopsis
The complex oxide Sr 7 Re 4 O 19 has been synthesized and its crystal structure was determined by X-ray di4raction powder data analysis (space group C2/m; a β«Ψβ¬ 13.6379(3) A > , b β«Ψβ¬ 5.6035(2) A > , c β«Ψβ¬ 10.3700(3) A > ;
β«Ψβ¬ 98.348(2)3, Z β«Ψβ¬ 2, R I β«Ψβ¬ 0.018, R P β«Ψβ¬ 0.050). The compound crystallizes in a new structure type, which can be derived from the Ba 7 Ir 6 O 19 structure by removing the Ir atoms from the middle octahedron of three face-sharing IrO 6 octahedra units. This change results in the in5nite cis-bridged chains of the ReO 6 octahedra linked together by common corners. Each chain is connected with another one by the corner-sharing of each second ReO 6 octahedron. The 10-and 12-coordinated Sr atoms are situated between these in5nite structure fragments. Magnetic properties of the Sr 7 Re 4 O 19 compound were studied by SQUID measurements.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Ba 2 CoBO 6 (B = Mo, W) perovskites have been prepared in polycrystalline form by thermal treatment, in air, of previously decomposed citrate precursors. These materials have been characterized by X-ray (XRD) and neutron powder diffraction (NPD) data and magnetization measurements. At room temperatu
## Abstract For Abstract see ChemInform Abstract in Full Text.