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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 1380-1384 
    ISSN: 0044-2313
    Keywords: silicon nitrides ; nitrido-silicates ; strontium ; barium ; synthesis ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Nitrido-Silicates. II. High Temperature Syntheses and Crystal Structures of Sr2Si5N8 and Ba2Si5N8Pure Sr2Si5N8 and Ba2Si5N8 were obtained by reaction of silicon diimide with metallic strontium and barium, respectively. The reactions have been carried out under nitrogen atmosphere in a specially developed high-frequency furnace at temperatures between 1 550 and 1 650°C. Sr2Si5N8 (Pmn21, a = 571.0(2), b = 682.2(2), c = 934.1(2) pm, Z = 2, R = 0.037, wR = 0.021) and Ba2Si5N8 (Pmn21, a = 578.3(2), b = 695.9(2), c = 939.1(2) pm, Z = 2, R = 0.022, wR = 0.018) are isotypic and contain M2+ ions as well as a three-dimensional covalent network structure of corner-sharing SiN4 tetrahedra. Two sorts of N occur with molar ratio 1 : 1 which are bonded to two and three Si, respectively. Predominantly, the N which are bonded to two Si belong to the coordination spheres of the M2+ ions.
    Notes: Sr2Si5N8 und Ba2Si5N8 werden phasenrein durch Umsetzung von Siliciumdiimid mit den jeweiligen Metallen Strontium bzw. Barium unter Stickstoffatmosphäre in einem speziellen Hochfrequenzofen bei 1 550 bis 1 650°C synthetisiert. Sr2Si5N8 (Pmn21, a = 571,0(2), b = 682,2(2), c = 934,1(2) pm, Z = 2, R = 0,037, wR = 0,021) und Ba2Si5N8 (Pmn21, a = 578,3(2), b = 695,9(2), c = 939,1(2) pm, Z = 2, R = 0,022, wR = 0,018) kristallisieren isotyp und sind aus M2+-Ionen (M = Sr bzw. Ba) sowie einer kovalenten dreidimensionalen Raumnetzstruktur eckenverknüpfter SiN4-Tetraeder aufgebaut. Je 4 N sind an zwei bzw. drei Si gebunden. Die an je zwei Si gebundenen N leisten den dominierenden koordinativen Beitrag für die M2+-Ionen.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 1037-1041 
    ISSN: 0044-2313
    Keywords: Silicon nitrides ; nitrido silicates ; synthesis ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Nitrido Silicates. I. High Temperature Synthesis and Crystal Structure of Ca2Si5N8Ca2Si5N8 is obtained by reaction of silicon diimide with metallic calcium under nitrogen atmosphere performed in a specially developed high-frequency furnace at temperatures between 1 500 and 1 600°C. Ca2Si5N8 (Cc, a = 1 435.2(3), b = 561.0(1), c = 968.9(2) pm, β = 112.06(3)°, Z = 4, R = 0.023, wR = 0.018) contains Ca2+ ions as well as a three-dimensional covalent network structure of corner-sharing SiN4 tetrahedra. Two sorts of N occur with molar ratio 1:1 which are bonded to two and three Si, respectively.
    Notes: Ca2Si5N8 wurde durch Umsetzung von Siliciumdiimid mit Calciummetall unter Stickstoffatmosphäre in einem speziell entwickelten Hochfrequenzofen bei 1 500 bis 1 600°C synthetisiert. Ca2Si5N8 (Cc, a = 1 435,2(3), b = 561,0(1), c = 968,9(2) pm, β = 112,06(3)°, Z = 4, R = 0,023, wR = 0,018) ist aus Ca2+-Ionen sowie einer kovalenten dreidimensionalen Raumnetzstruktur eckenverknüpfter SiN4-Tetraeder aufgebaut. Je 4 N sind zweifach bzw. dreifach an Si gebunden.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 1535-1538 
    ISSN: 0044-2313
    Keywords: Silicon nitrides ; nitrido-silicates ; cerium ; crystal structure ; magnetic susceptibility ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Nitrido-silicates. III [1] High-Temperature Synthesis, Crystal Structure, and Magnetic Properties of Ce3[Si6N11]Pure Ce3[Si6N11] was obtained as transparent yellow crystals by reaction of metallic cerium with silicon diimide (Ce:Si = 1:2) under nitrogen atmosphere in a specially developed high-frequency furnace at 1660°C. Ce3[Si6N11] (P4bm, a = 1013.7(3), c = 483.9(5) pm, Z = 2, R = 0.034, wR = 0.024) contains Ce3+ ions as well as a three-dimensional covalent anionic network structure of corner-sharing SiN4 tetrahedra. Measurements of the magnetic susceptibility gave no indications for magnetic ordering phenomena in the temperature range between 2 and 300 K. Above 100 K pure Curie-Weiss behaviour (μeff = 2,10 μB, determined at room temperature) was observed.
    Notes: Transparent gelbe Kristalle von Ce3[Si6N11] wurden phasenrein durch Umsetzung von metallischem Cer mit Siliciumdiimid (Ce:Si = 1:2) unter Stickstoffatmosphäre in einem speziellen Hochfrequenzofen bei 1660°C synthetisiert. Ce3[Si6N11] (P4bm, a = 1013,7(3), c = 483,9(5) pm, Z = 2, R = 0,034, wR = 0,024) besteht im Festkörper aus Ce3+-Ionen sowie einer kovalenten, dreidimensional vernetzten Anionenteilstruktur eckenverknüpfter SiN4-Tetraeder. Messungen der magnetischen Suszeptibilität ergaben keine Hinweise auf magnetische Ordnungsphänomene im Temperaturbereich von 2 bis 300 K. Oberhalb 100 K wurde reines Curie-Weiss-Verhalten (μeff = 2,10 μB, ermittelt bei Raumtemperatur) beobachtet.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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