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  • 1
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation of organosilicon compounds. 47. The crystal land molecular structure of 1,3,5,7-tetramethyl-tetrasila-adamantan1,3,5,7- Tetramethyl-tetrasila-adamantan, Si4C10H24, is a pyrolysis product of Si(CH3)4. It crystallizes in the monoclinic space group P21/c with a = 8.859 Å, b = 9.844 Å, c = 18.316 Å, β = 91.04°, Z = 4. The molecule exhibits Td-symmetry within the experimental error. The mean bond lengths Si—C are 1.889 Å and 1.866 Å for the Si—CH3 and Si—CH2 bonds respectively.
    Notes: Das bei der Pyrolyse von Si(CH3)4 gebildete 1,3,5,7- Tetramethyltetrasila-adamantan Si4C10H24 Kristallisiert monoklin in der Raumgruppe P21/c mit a = 8,859 Å, b = 9,844 Å, c = 18,316 Å, β = 91,04°, Z = 4. Das Molekül besitzt innerhalb der Fehlergrenzen Td-Symmetrie. Die mittleren Bindungslängen Si—C betragen 1,889 Å bzw. 1,866 Å für Bindungen Si—CH3 bzw. Si—CH2.
    Additional Material: 2 Ill.
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  • 2
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation of Organosilicon Compounds. LXI. Crystal and Molecular Structure of 1.1.3.3.5.5.7.7-Octamethyl-1.3.5.7-tetrasila-cyclooctane Si4C12H32Octamethyl-tetrasila-cyclooctan Si4C12H32 crystallizes in the monoclinic space group C2 with a = 17.807, b = 6.121, c = 10.856 Å, β = 126.09° und 2 molecules in the unit cell. The molecule has a C2-conformation which deviates slightly from C2v symmetry. The mean Si—C bond length is 1.879 ± 0.011 Å. The mean Si—CH2 bond length is greater than the Si—CH3 bond length (1.897(15) Å and 1.861(10) Å respectively).
    Notes: Octamethyl-tetrasila-cyclooctan Si4C12H32 kristallisiert monoklin in der Raumgruppe C2 mit a = 17,807, b = 6,121, c = 10,856 Å, β = 126,09° und Z = 2. Die Molekel liegt in einer C2-Konformation vor, die von der Symmetrie C2v nur wenig abweicht. Die mitteleren Si-C-Bindungsabstände betragen 1,879 ± 0,011 Å. Die mitteleren Si-CH2 Abstände sind mit 1,897 (15) Å größer als die Si-CH3-Abstände (1,861(10) Å). Die Bindungswinkel im Ringsystem zeigen signifikante Abweichungen von Tetraederwinkeln.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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