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  • Inorganic Chemistry  (2)
  • 1965-1969  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 363 (1968), S. 305-311 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: New silylamine esters (m. p.' s 〈 150°C) have been prepared by condensation of excess diorganodichlorosilanes with diphenols in the presence of amine catalysts, followed by interacting the terminal chloro groups with ammonia and primary amines, respectively. Si-phenylsilazane esters with free terminal amino groups are formed as silylamines, whereas silazane esters with alkyl-substituted silicon react to yield polysilazane-polysilicic acid esters.
    Notes: Neue veresterte Silylamine mit Fließpunkten unter 150°C wurden hergestellt durch Kondensation von überschüssigen Diorganodichlorsilanen mit Diphenolen in Gegenwart von Aminkatalysatoren. Die Chlorendgruppen werden anschließend mit Ammoniak bzw. primären Aminen umgesetzt. Es wurde gefunden, daß Si-phenylsilazanester mit freien Aminoendgruppen als Silylamine anfallen, dagegen bilden Silazanester mit alkyl-substituiertem Silicium Polysilazanpolykieselsäureester.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 371 (1969), S. 23-31 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: New tert.-butoxy-(halogenphenoxy)-silanes, being stable towards hydrolysis in ln HCl, have been prepared by reaction of N, N-dimethylaminosilanes with halogenphenols. Some of these new compounds have been investigated by means of DTA techniques.
    Notes: Es wurden neue, in 1n HCl hydrolysebeständige Tertiärbutoxy-(halogenphenoxy)-silane durch Reaktion von entsprechenden N, N-Dimethylaminosilanverbindungen mit halogenierten Phenolen hergestellt. Einige dieser Verbindungen wurden mittels DTA auf ihre thermische Stabilität untersucht.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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