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  • Articles: DFG German National Licenses  (2)
  • 1990-1994  (2)
  • 1925-1929
  • 1830-1839
  • 1993  (2)
  • Dibromides  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 619 (1993), S. 1374-1378 
    ISSN: 0044-2313
    Keywords: Metallothermic Reduction ; Dibromides ; Diiodides ; Ternary Halides ; Dysprosium ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metallothermic Reduction of the Tribromide and -iodide of Dysprosium with Alkali MetalsMetallothermic reduction (900-1000°C, 2-3 d, tantalum capsules) of DyX3 (X = Br, I) with alkali metals (A = Li—Cs) results in the case of lithium and sodium (except for the system DyBr3/Li) in the formation of the dihalides DyX2 (DyI2 with the CdCl2-type, DyBr2 with the SrI2-type of structure). The reduction of DyI3 with potassium leads to K1.71DyI4 which crystallizes hexagonally with a = 1 446.7(2) pm and c = 473.3(1) pm, space group P62m (Z = 3). In K1.71DyI4, [DyI6]-octahedra are edge-connected forming chains along [001] that are linked via K+. With A = K, Rb, Cs, variants of the perovskite-type of structure with the composition ADyX3 are obtained. They crystallize with the tetragonal NaNbO3-II-type (CsDyBr3) or with the orthorhombic GdFeO3-type of structure (KDyBr3, RbDyX3, CsDyI3).
    Notes: Bei der metallothermischen Reduktion (Tantalampulle, 900-1 000°C, 2-3 d) von DyX3 (X = Br, I) mit den Alkalimetallen (A = Li—Cs) erhält wird im Falle von Lithium und Natrium (außer im System DyBr3/Li) die Dihalogenide DyX2 (DyI2 im CdCl2-Typ, γyBr2 im SrI2-Typ). Die Reduktion von DyI3 mit Kalium führt zu K1,71DyI4, das hexagonal mit a = 1 446,7(2) pm, c = 473,3(1) pm, Z = 3 in der Raumgruppe P62m kristallisiert: [DyI6]-Oktaeder werden über Kanten längs [001] zu Ketten verknüpft, die durch K+-Ionen verbunden werden. Die Reduktion von DyBr3 mit Kalium, Rubidium und Caesium bzw. DyI3 mit Rubidium und Caesium führen zu Perowskitvarianten ADyX3, die bis auf CsDyBr3 (tetragonaler NaNbO3-II-Typ), im orthorhombischen GdFeO3-Typ kristallisieren.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 619 (1993), S. 1379-1383 
    ISSN: 0044-2313
    Keywords: Metallothermic Reductions ; Dibromides ; Diiodides ; Ternary Halides ; Neodymium ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metallothermic Reduction of the Tribromide and -iodide of Neodymium with Alkali MetalsMetallothermic reduction (700-800°C, 2-3d, tantalum capsules) of NdX3 (X = Br, I) with an equimolar amount of alkali metal (A = Li—Rb) results in the case of lithium and sodium (except for the system Li/NdBr3) in the formation of the dihalides NdX2 (NdBr2 with the PbCl2-type, NdI2 with the SrBr2-type of structure). With A = K and Rb, KNd2Br5, RbNd2Br5, RbNd2I5 and “K8Nd7I25” are obtained. The first three crystallize with the monoclinic TlPb2Cl5-type (space group P21/c), the latter with the orthorhombic K2PrCl5-type of structure (space group Pnma) containing both Nd3+ and Nd2+.
    Notes: Die metallothermische Reduktion (700-800°C, 2-3d, Tantalampulle) von NdX3 (X = Br, I) mit äquimolaren Mengen an Alkalimetall (A = Li—Rb) führt im Falle von Lithium und Natrium (mit Ausnahme von NdBr3/Li) zu den Dihalogeniden NdX2 (NdBr2 im PbCl2-Typ, NdI2 im SrBr2-Typ). Bei der Umsetzung mit Kalium und Rubidium erhält man KNd2Br5, RbNd2Br5 bzw. RbNd2I5, die im monoklinen TlPb2Cl5-Typ (Raumgruppe P21/c) kristallisieren, sowie das isostrukturelle “K8Nd7I25”, das neben Nd2+ auch Nd3+ enthält und zum K2PrCl5-Typ gehört (orthorhombisch, Raumgruppe Pnma).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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