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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 74 (1987), S. 342-343 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 75 (1988), S. 140-141 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 559 (1988), S. 208-208 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 573 (1989), S. 107-118 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: „LaTa5O14“, a Derivative of the Tetragonal Tungsten Bronzes. Preparation and Structure„LaTa5O14“ single crystals were synthesized for the first time by heating mixtures La2O3/Ta2O5 (1:5) at temperatures of T = 1 685°C in air. „LaTa5O14“ crystallizes in the orthorhombic space group Cmmm with a = 16.977(1) Å, b = 17.594(1) Å and c = 3.8480(4) Å. The structure was refined to give R = 6.36% and Rw = 3.27%. The Ta atoms are partly surrounded by O octahedrally, partly pentagonal-bipyramidal. The unit cell is built up by layers of composition [Ta22O62]14- connected along the [001] direction with holes filled up totally or partly with La. The relationship to the tetragonal tungsten bronzes will be discussed.
    Notes: Im System La2O3/Ta2O5 gelang erstmals die Darstellung von gelben „LaTa5O14“-Einkristallen durch Tempern der Gemenge La2O3/Ta2O5 (1:5) bei T = 1 685°C an Luft. „LaTa5O14“ kristallisiert orthorhombisch in der Raumgruppe Cmmm mit den Gitterkonstanten a = 16,977(1) Å, b = 17,594(1) Å und c = 3,8480(4) Å. Die Struktur wurde bis R = 6,36% bzw. Rw = 3,27% verfeinert. Ta(1), Ta(3) und Ta(4) sind oktaedrisch, Ta(2) ist pentagonal-bipyramidal von O umgeben. Schichten aus diesen Polyedern sind über O-Teilchen entlang [001] miteinander eckenverknüpft. Vom Ta-O-Netzwerk der Zusammensetzung [Ta22O62]14- gebildete Lücken sind ganz oder teilweise mit La-Teilchen gefüllt; die Verbindung besitzt deshalb nur annähernd die Zusammensetzung LaTa5O14. Eine Verwandtschaft zu den tetragonalen Wolframbronzen ist erkennbar.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 587 (1990), S. 208-208 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 588 (1990), S. 43-54 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chemical Transport Reactions of Compounds LnTa7O19 (Ln = La—Nd) and Structure Refinement of NdTa7O19Crystals of compounds LnTa7O19 (Ln = Na—Nd) could be obtained by chemical transport reactions (T2 → T1; T2 = 1100°C, T1 = 1000°C) using chlorine (p(Cl2; 298 K) = 1 atm) as transport agent. An increase of transport rate and an improvement of crystal growth was observed if small amounts of vanadium metal were added. Solid state reactions with mixtures of Ln2O3/Ta2O5 (1:7) in air (T ≈ 1400-1500°C), however, were not succesful because the resulting samples contained LnTa7O19 with other ternary phases as by-products. NdTa7O19 crystallizes in the well-known LaTa7O19-type structure with cell dimensions of a = 6.2229(3) Å, c = 19.939(2) Å and Z = 2. The crystal structure was refined in space groups P6c2 (R = 3.35%, RW = 2.67%) and P63/mcm (R = 4.75%, RW = 3.88%). Taking aspects of structural chemistry, x-ray results and MAPLE calculations into account, however, the spacegroup P6c2 should be preferred.
    Notes: Durch chemischen Transport (T2 → T1; T2 = 1100°C, T1 = 1000°C) mit dem Transportmittel Chlor (p(Cl2; 298 K) = 1 atm) wurden Kristalle der Verbindungen LnTa7O19 (Ln = La—Nd) in der Senke bei T1 erhalten. Durch geringe Zusätze von metallischem Vanadium konnte die Transportrate erhöht sowie das Kristallwachstum wesentlich verbessert werden. Umsetzungen von Gemengen Ln2O3/Ta2O5 (1:7) an Luft (T ≈ 1400-1500°C) ergaben nur unvollständig umgesetzte Präparate mit einem Anteil von LnTa7O19 (Ln = La—Nd). NdTa7O19 kristallisiert hexagonal im bekannten LaTa7O19-Typ mit den Gitterkonstanten a = 6,2229(3) Å, c = 19,939(2) Å und Z = 2. Die Struktur wurde in den Raumgruppen P6c2 (R = 3,35%, RW = 2,67%) und P63/mcm (R = 4,75%, RW = 3,88%) verfeinert. Die sich hierbei ergebenden Strukturmodelle werden miteinander verglichen, wobei aufgrund röntgenographischer und kristallchemischer Aspekte sowie aufgrund eines Vergleichs der MAPLE-Werte das Modell in P6c2 vorgezogen wird.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Thermal Behaviour of Ln2CeTaO6Cl3 (Ln=La—Nd) and Ce3TaO5(OH)Cl3; Structure and Phase-Width of the Decomposition Product “La2Cex3+Ce1-x4+TaO6Cl3-x”The new mixed-valenced phases of composition Ln2Cex3+Ce1-x4+TaO6Cl3-x (Ln = La, Ce) were obtained by heating samples of oxochlorotantalates Ln2CeTaO6Cl3 (Ln = La, Ce; hex.) in evacuated silica tubes (T ≈ 1050°C). The observed thermal decomposition of Ln2CeTaO6Cl3 (Ln = La, Ce) lead to the formation of chlorine according to redox-reactions. Chemical transport experiments (T2 → T1; T2 = 1100°C, T1 = 1000°C) with chlorine as transport agent were used to prepare needle-like single crystals of the above-mentioned phases.Ln2Cex3+Ce1-x4+TaO6Cl3-x (Ln = La, Ce) crystallizes in the monoclinic space group Cm with cell-dimensions a = 35.283(6), b = 5.429(1), c = 9.517(2) Å and β = 98.92(2)° (Z = 8). The structure was refined to give R = 6.07% (Rw = 5.95%).Building units are especially chains of face-sharing Cl6-octahedra connected along [010] as well as TaO6-polyhedra with slightly distorted trigonally prismatic environment for Ta. Thus, main structures features related to the starting material La2CeTaO6Cl3 were preserved, so that the thermal decomposition can be regarded as a topotactic reaction.The model of a phase-width concerning the Cl- as well as the LaCl3-content will be discussed based on crystal structure investigations.Furthermore, the new hexagonal phase Ce3TaO5(OH)Cl3 which crystallizes in the well-known La3TaO5Cl3-type structure could be prepared by hydrogen reduction of mixed-valenced Ce3TaO6Cl3 in closed silica ampoules. The thermal behavior in air was investigated utilizing a high-temperature Guinier focusing camera. The cell-dimensions of compounds Ln3TaO5(OH)Cl3 and Ln2CeTaO6Cl3 (Ln = La—Nd) were refined and discussed.
    Notes: Durch thermischen Abbau (T ≈ 1050°C) von Oxochlorotantalaten Ln2CeTaO6Cl3 (Ln = La, Ce; hex.) entstanden unter Abspaltung von Chlor die neuen Phasen Ln2Cex3+Ce1-x4+TaO6Cl3-x (Ln = La, Ce). Einkristalle aller genannten Verbindungen wurden durch chemischen Transport (T2 → T1; T2 = 1100°C, T1 = 1000°C; Transportmittel Chlor) zugänglich. Nach der Strukturbestimmung kristallisiert La2Cex3+Ce1-x4+TaO6Cl3-x monoklin in der Raumgruppe Cm mit a = 35,283(6), b = 5,429(1), c = 9,517(2) Å, β = 98,92(2)°, Z = 8 mit R = 6,07% (Rw = 5,95%). Neben Strängen aus miteinander über Flächen verknüpften Cl6-Oktaedern enthält die Struktur TaO6-Baugruppen mit trigonal-prismatischer Koordination. Damit bleiben wesentliche Merkmale der hexagonalen Ausgangsstruktur von La2CeTaO6Cl3 erhalten, so daß der thermische Abbau zu Ln2Cex3+Ce1-x4+TaO6Cl3-x (Ln = La, Ce) auch als topotaktische Reaktion angesehen werden kann.Das Modell einer Phasenbreite bezüglich des Cl- sowie des LaCl3-Gehaltes wird auf der Grundlage detaillierter Strukturinformationen diskutiert.Ce3TaO5(OH)Cl3, eine neue, zu La3TaO5(OH)Cl3 (hex.) isostrukturelle, thermisch weniger beständige Cer3+-Verbindung konnte unter reduzierenden Bedingungen dargestellt werden. An der Luft tritt Oxydation zu Ce3TaO6Cl3 bereits bei T = 210°C ein. Die Zellparameter von Ce3TaO5(OH)Cl3 und weiteren Vertretern der Strukturfamilien Ln3TaO5(OH)Cl3 und Ln2CeTaO6Cl3 (Ln = La—Nd) werden verglichen und diskutiert.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 591 (1990), S. 107-117 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Crystal Structure of Ln3TiO4Cl5 (Ln = La-Nd) - the First Oxochlortitanates of Rare EarthThe compounds Ln3TiO4Cl5 have been prepared by reaction of LnCl3/LnOCl/TiO2 (1:2:1) (Ln = La-Nd) in evacuated silica ampoules. Single crystals of La3TiO4Cl5 were obtained by chemical transport reaction (T2 → T1; T2 = 1050°C, T1 = 950°C) using chlorine (p(Cl2; 298 K) = 1 atm) and sulfur as transport agents with La2TiO5 as starting material.La3TiO4Cl5 crystallizes in the orthorhombic space group Pnma (No. 62) with cell-dimensions a = 16.760(2) Å, b = 4.0991(6) Å, c = 14.634(2) Å, Z = 4. The structure was refined to give R = 4.76%, Rw = 2.47%. Main building units are TiO5 trigonal bipyramides and threefold capped trigonal prisms around La. The relationship to La2TaO4Cl3 will be discussed.
    Notes: Die neuen Verbindungen Ln3TiO4Cl5 wurden durch Umsetzung von Gemengen LnCl3/LnOCl/TiO2 (1:2:1) (Ln = La-Nd) in evakuierten Quarzglasampullen dargestellt (8d; 800°C). Einkristalle (mit Ln = La) wurden durch chemischen Transport (T2 → T1;T2 = 1050°C; T1 = 950°C) mit La2TiO5 als Startbodenkörper bei T2 sowie mit einer halogenierenden Transportmittelkombination aus Chlor (p)Cl2, 298K = 1 atm) und Schwefel (0,04 mmol Schwefel auf 1,36 mmol La2TiO5) erhalten.La3TiO4Cl5 kristallisiert orthorhombisch: RG Pnma (No. 62) mit den Gitterkonstanten a = 16,760(2) Å, b = 4,0991(6) Å, c = 14,634(2) Å, Z = 4. Die Struktur wurde bis zu R = 4,76%, Rw = 2,47% verfeinert. Die Koordination der Metallteilchen läßt sich durch trigonale Bipyramiden (TiO5 und dreifach bekappte trigonale Prismen (LaO2Cl4Cl3) beschreiben. Man erkennt ferner trigonale Baugruppen [La3Tio4]5+, die in eine Matrix aus Cl-Teilchen „eingebettet“ sind und somit eine Strukturverwandtschaft mit La2TaO4Cl3 zeigen.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 561 (1988), S. 192-192 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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