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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 589 (1990), S. 129-138 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal Structure of K4[SiO4]Colourless crystals of K4[SiO4] which are isotypic with Cs4[SnO4] resulted by heating of well ground mixtures of KO0,55 and SiO2 [K:Si = 4.4: 1.0; 700°C; 7 d] in tightly closed Ni-tubes. The crystal structure was solved by fourcycle-diffractometer data [Siemens AED2, 1814 I0(h kl), space group P21/c with a = 1037.0(3) pm, b = 639.2(1) pm, c = 1036.6(3) pm, β = 112.83(2)°, Z = 4, R = 8.0%, Rw = 4.5%]. The Madelung Part of Lattice Energy, MAPLE, and Effective Coordination Numbers, ECoN, calculated via Mean Fictive Ionic Radii, MEFIR, are given. The isotypism of the compounds mentioned above is compared graphically.
    Notes: Farblose, mit Cs4[SnO4] isotype Kristalle von K4[SiO4], entstehen beim Tempern inniger Gemenge von KO0,55 und SiO2 [K:Si = 4,4:1,0; 700°C 7 d] in fest verschlossenen Ni-Bömbchen. Die Kristallstruktur wurde über Vierkreisdiffraktometerdaten [Siemens AED2, 1814 I0(hkl), Raumgruppe P21/c mit a = 1037,0(3) pm, b = 639,2(1) pm, c = 1036,6(3) pm, β = 112,83(2)°, Z = 4, R = 8,0%, RW = 4,5%] aufgeklärt. Der Madelunganteil der Gitterenergie, MAPLE, sowie Effektive Koordinationszahlen, ECoN, diese über Mittlere Fiktive Ionenradien, MEFIR, berechnet, werden angegeben. Ein Isotypievergleich der beiden oben genannten Verbindungen erfolgt graphisch.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 587 (1990), S. 145-156 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: An Oxostannate of a New Structure Type: Cs4[SnO4]In order to prepare Cs3LiSnO4 by heating of a well ground mixture of the binary oxides [CsO0.67, Li2O, SnO2; Cs:Li:Sn = 3.3:1.0:1.0; 450°C; 28 d; Ni-tube] colourless, monoclinic single crystals of Cs4[SnO4] have been yielded for the first time: space group P21/c with a = 1180.8 pm. b = 728.2 pm, c = 1166,7 pm, β = 111.79°, Z = 4. The crystal structure was solved by fourcycle-diffractometer data [Siemens AED2, 2299 from 2708 I0(hkl), R = 7.0%, Rw = 5.6%], parameters see text. Characteristic for the complicated structure are “isolated” [SnO4]4- tetrahedra. Mean Fictive Ionic Radii, MEFIR, Effective Coordination Numbers, ECoN and the Madelung Part of Lattice Energy, MAPLE, have been calculated.
    Notes: Bei dem Versuch, Cs3LiSnO4 darzustellen, erhielten wir farblose, monokline Einkristalle von Cs4[SnO4] aus innigen Gemengen von CsO0,67, Li2O und SnO2 [Cs:Li:Sn = 3,3:1,0:1,0; 450°C; 28 d; Ni-Bombe]: Raumgruppe P21/c mit a = 1180,8 pm, b = 728,2 pm, c = 1166,7 pm, β = 111,79°, Z = 4.Die Kristallstruktur wurde mittels Vierkreisdiffraktometerdaten [Siemens AED2, 2299 von 2708 I0(hkl), R = 7,0%, Rw = 5,6%] bestimmt, Parameter siehe Text. Charakteristisch, für den im Ganzen komplizierten Aufbau sind „isolierte“ tetraedrische Gruppen [SnO4]4-. Mittlere Fiktive Ionenradien, MEFIR, Effektive Koordinationszahlen, ECoN, sowie der Madelunganteil der Gitterenergie, MAPLE, wurden berechnet.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 593 (1991), S. 17-34 
    ISSN: 0044-2313
    Keywords: Cesium Lithium Orthotitanate, Silicate ; Crystal Structure ; Schlegel Diagrams ; MAPLE Calculations ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Isotypism of Titanates and Silicates: About Cs2Li2[SiO4] and Cs2Li2[TiO4]For the first time colourless single crystals of Cs2Li2[SiO4] have been prepared by heating of a well ground mixture of the binary oxides CsO0.67, LiO0.5 and SiO2[Cs:Li:Si = 2.2:2.0:1.0; 450°C; 21 d] in tightly closed Ni tubes. The new oxosilicate crystallizes triclinic (space group P1 with a = 959.6(3), b = 577.4(2), c = 558.1(2) pm, α = 92.52(3)°, β = 110.93(3)°, γ = 94.45(3)°, Guinier-Simon powder data). The crystal structure was determined by four-circle diffractometer data [Siemens AED 2, 1612 I°(hkl), Z = 2, R = 7.2%, Rw = 6,5%], parameters see text.Cs2Li2[TiO4] has also been prepared as colourless single crystalls from CsO0.56, LiO0.5 und TiO2 (Cs:Li:Ti = 2.3:2.2:1.0; 650°C; 68 d, Ni tube) and investigated by x-ray [four-circle diffractometer data, Philips PW 1100, 2193 from 2383 I°(hkl). Z = 2, R = 7.6%, Rw = 6.1%, space group P1 with a = 951.0(1), b = 594.5(1), c = 582.6(1) pm, α = 93.11(1)°, β = 110.37(1), γ = 95.04(1)°, Guinier-Simon powder data]. The Madelung Part of Lattice Energy, MAPLE, and Effective Coordination Numbers, ECoN, these via Mean Fictive Ionic Radii, MEFIR, have been calculated. A detailed comparison of the structures is carried out.
    Notes: Erstmals wurden farblose Einkristalle von Cs2Li2[SiO4] durch Tempern inniger Gemenge der binären Oxide CsO0,67, LiO0,5 und SiO2 [Cs:Li:Si = 2,2:2,0:1,0; 450°C; 21 d] in fest verschlossenen Ni-Bömbchen erhalten. Es liegt Isotypie mit Rb2Li2[MO4] (M = Si, Ge, Ti) vor: triklin (Raumgruppe P1) mit a = 959,6(3) pm, b = 577,4(2) pm, c = 558,1(2) pm, α = 92,52(3)°, β = 110,93(3)°, γ = 94,45(3)°, (Guinier-Simon-Daten). Die Kristallstruktur wurde mittels Vierkreisdiffraktometerdaten aufgeklärt [Siemens AED 2, 1612 I°(hkl), Z = 2, R = 7,2%, Rw = 6,5%], Parameter siehe Text.Ebenfalls neu wurde Cs2Li2[TiO4] in Form farbloser Einkristalle durch Tempern inniger Gemenge von CsO0,56, LiO0,5 und TiO2 [Cs:Li:Ti = 2,3:2,2:1,0; 650°C; 68 d, Ag-Bömbchen] dargestellt und röntgenographisch untersucht. Die Strukturverfeinerung [Vierkreisdiffraktometerdaten, Philips PW 1100, 2193 von 2383 I°(hkl), Z = 2, R = 7,6%, Rw = 6,1%, Raumgruppe P1 mit a = 951,0(1) b = 594,5(1), c = 582,6(1) pm, α = 93,11°(1), β = 110,37(1)°, γ = 95,04(1)° Guinier-Simon-Daten] bestätigt auch hier Isotypie mit Rb2Li2[SiO4]. Der Madelunganteil der Gitterenergie, MAPLE, sowie Effektive Koordinationszahlen, ECoN, diese über Mittlere Fiktive Ionenradien, MEFIR, wurden berechnet. Für die nun bekannten Vertreter dieses Typs wurde ein Isotypievergleich vorgenommen.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 571 (1989), S. 101-112 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The First Quaternary Oxostannate with Isolated Anion Structure: RbNa3[SnO4]For the first time colourless single crystals of RbNa3SnO4 which are isotypic with NaLi3SiO4 and NaLi3GeO4 [2] have been prepared by heating e.g. a well ground mixture of RbSn and Na2O2 [Rb : Na = 1 : 4.0; 750°C; 21 d; Ni-tube]. The crystal structure was solved by four-cycle-diffractometer data [Siemens AED2; 1801 I0(hkl); space group I41/a; Z = 16; a = 1279.57, c = 1510.85 pm; R = 5.7%; Rw = 4.4%]. Mean Fictive Ionic Radii, MEFIR, Effective Coordination Numbers, ECoN, and the Madelung Part of Lattice Energy, MAPLE, are calculated. The isotypism of the compounds mentioned above is compared graphically.
    Notes: Erstmals wurde das mit NaLi3SiO4 und NaLi3GeO4 [2] isotype Oxostannat RbNa3SnO4 in Form farbloser Einkristalle, z. B. aus Gemengen von RbSn und Na2O2 [Rb : Na = 1 : 4,0; 750°C; 21 d; Ni-Bombe], dargestellt. Die Kristallstruktur wurde über Vierkreisdiffraktometerdaten [Siemens AED2; 1801 I0(hkl); Raumgruppe I41/a; Z = 16; a = 1279,57, c = 1510,85 pm; R = 5,7%; Rw = 4,4%] aufgeklärt. Mittlere Fiktive Ionenradien, MEFIR, Effektive Koordinationszahlen, ECoN, sowie der Madelunganteil der Gitterenergie, MAPLE, wurden berechnet. Ein Isotypievergleich der drei oben genannten Verbindungen erfolgt graphisch.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 592 (1991), S. 93-105 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: A “Lithosilicate” with Columnar Units: RbLi5{Li[SiO4]}2In order to prepare RbLi3[SiO4] single crystals of RbLi5{Li[SiO4]}2 have been obtained for the first time by heating of a well ground mixture of the binary oxides RbO0.68, LiO0.5 and SiO2 [Rb:Li:Si = 1.1:3.0:1.0; 600°C; 21 d] in tightly closed Ni tubes. The new “lithosilicate” crystallizes monoclinic (space group C2/m with a = 1563.1(2) pm, b = 635.4(1) pm, c = 776.3(1) pm, β = 90.53(1)°, Guinier-Simon powder data). The crystal structure was determined by four-cycle diffractometer data [Philips PW 1100, 1237 from 1609 Io(hkl), Z = 4, R = 9.2%, Rw = 8.3%], parameters see text. The Madelung Part of Lattice Energy, MAPLE, and Effective Coordination Numbers, ECoN, these via Mean Fictive Ionic Radii, MEFIR, have been calculated.
    Notes: Bei dem Versuch, RbLi3[SiO4] darzustellen, entstanden erstmals Einkristalle von RbLi5{Li[SiO4]}2 durch Tempern inniger Gemenge der binären Oxide RbO0,68, LiO0,5 und SiO2 [Rb:Li:Si = 1,1:3,0:1,0; 600°C; 21 d] in fest verschlossenen Ni-Bömbchen. Das neue „Lithosilicat“ kristallisiert monoklin (Raumgruppe C2/m mit a = 1563,1(2) pm, b = 635,4(1) pm, c = 776,3(1) pm, β = 90,53(1)°, Guinier-Simon-Daten). Die Kristallstruktur wurde mittels Vierkreisdiffraktometerdaten aufgeklärt [Philips PW 1100, 1237 von 1609 Io(hkl), Z = 4, R = 9,2%, Rw = 8,3%], Parameter siehe Text. Der Madelunganteil der Gitterenergie, MAPLE, sowie Effektive Koordinationszahlen, ECoN, diese über Mittlere Fiktive Ionenradien, MEFIR, wurden berechnet.
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  • 6
    Publication Date: 1989-01-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
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  • 7
    Publication Date: 1990-08-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
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  • 8
    Publication Date: 1990-10-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
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  • 9
    Publication Date: 1991-02-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
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  • 10
    Publication Date: 1991-01-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
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