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On the Knowledge of RbTaO3 – a New Type of a Layer Structure RbTaO3 crystallizes monoclinic with a = 9.589, b = 8.505, c = 8.135 Å, β = 94.87°, Z = 8, space group C2/m. The crystal structure (Fourcircle-diffractometer data, 4° ≤ Θ ≤ 33°, 1014 hkl, MoKα, R = 9,9%) shows sheets [TaO3] connected by Rb; one half of Ta is surrounded by O octahedrally, the other part tetragonal-pyramidal. Effective Coordination Numbers, ECoN, and the Madelung Part of Lattice Energy, MAPLE, have been calculated and are discussed.  相似文献   

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LiDy2Cl5, an Intermediate of the Metallothermic Reduction of DyCl3 with Lithium LiDy2Cl5 has been obtained via 2 Li + 2 DyCl3 = LiDy2Cl5 + LiCl as black single crystals (700°C, 1 week, sealed tantalum container) and crystallizes monoclinic with a = 1545.6(7), b = 659.2(2), c = 728.7(3) pm, β = 95.79(3)°, Z = 4, C2/c. Octahedra [LiCl6] are connected via common corners to rings [Li4Cl20], these parallel (100) to layers [LiCl4]. Bicapped trigonal prisms [DyCl8] are connected to a three-dimensional network [(DyCl13/3Cl23/3Cl32/4)] ? [Dy2Cl5].  相似文献   

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Cycloaddition of Dithiocyanogen and Trithiocyanogen with Hexafluoroacetone and Products of the Cleavage of the Sulfur-Sulfur Bond in Dithiocyan-Hexafluoroacetone Adduct by Elemental Chlorine The reaction of dithiocyanogen and trithiocyanogen with hexafluoroacetone (HFA) leads to the cycloaddition products (SCN)2 · 4 HFA 1 and S(SCN)2 · 4 HFA 2 . These are the first reactions of (SCN)2 and S(SCN)2 without cleavage of the S—S bonds. Elemental chlorine cleaves in 1 the S? S bond and 3 is formed. In 3 the chlorine atom can be replaced by the rests —CN 4 , (C6H11)2N— 5 , and n-C4H9– 6. 6 eliminates one molecule of HFA by warming up and the four-membered ring 7 is formed. The compounds were characterized on the basis of mass and nmr spectra.  相似文献   

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