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 crystal
Preparation, Structure, and Magnetic Studies of a New Sr11Re4O24 Double Oxide
β Scribed by K.G. Bramnik; G. Miehe; H. Ehrenberg; H. Fuess; A.M. Abakumov; R.V. Shpanchenko; V.Yu. Pomjakushin; A.M. Balagurov
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 300 KB
- Volume
- 149
- Category
- Article
- ISSN
- 0022-4596
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β¦ Synopsis
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 neutron powder diffraction data ( 2 β«Ψβ¬ 1.85). The compound has a cation-de5cient perovskite-related structure where cation vacancies are located at the A-sublattice. Re and Sr atoms occupy B-positions in an ordered 99rock-salt:: manner. The perovskite framework is strongly distorted due to rotation of ReO 6 octahedra, leading to a formation of the eightfold coordination for Sr atoms in Bpositions. An ordered arrangement of Re Ψ6 and Re Ψ7 cations is proposed on the basis of di4erent average Re+O distances. The Sr 11 Re 4 O 24 structure could be considered as a Ca 11 Re 4 O 24 type of perovskite structure distortion. A magnetic order of Sr 11 Re 4 O 24 (ferro-or ferrimagnetic) is observed from SQUID measurements (T C β«Ψβ¬ 12.0 K). A moment of β«Ψβ¬ 0.80 B is derived from the paramagnetic region (30+200 K) for Re 6Ψ
π SIMILAR VOLUMES
Single crystals of a new reduced calcium niobium oxide, CaNb 2 O 4 , were prepared in an evacuated quartz tube at 11003C. The calcium niobium oxide crystallizes in the orthorhombic space group Pbcm with a β«Ψβ¬ 5.054(1), b β«Ψβ¬ 11.904(1), and c β«Ψβ¬ 5.839(1) A s , Z β«Ψβ¬ 4, and the 5nal R factors are R β«
new title compound are obtained from a mixture of La2O3, B2O3, and LaF3 in the molar ratio 5:6:2 (Walker-type multianvil apparatus, 6 GPa, 1300 Β°C, 10 min). La4B4O11F2 crystallizes in the monoclinic space group P21/c with Z = 8. The crystal structure contains BO3 groups connected by BO4 tetrahedra v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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