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  • 1
    ISSN: 1434-4475
    Keywords: Disiloxanes ; Organylaminosilanes ; Alkanolysis ; Mass spectra interpretation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Reaction of hexachlorodisiloxane with primary and secondary amines leads — in dependence of stoichiometry — to numerous partially and totally organylamino substituted disiloxanes. Partially aminosubstituted chlorodisiloxanes are very sensitive to moisture and can be converted into disiloxanes with different organylamino groups. Exhaustive alkanolysis substitutes amino as well as chloro groups giving hexaalkoxydisiloxanes, but partial alkanolysis may substitute amino in preference to chloro groups. Mass spectra can be interpreted by abstraction ofRR′N·,RR′N+,RR′NH and (RR′N minus H) units. Most of the compounds are colourless liquids but hexakis(piperidino)-disiloxane melts at 270 °C.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 336 (1994), S. 218-224 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetic Investigation of the Platinum-catalysed Hydrosilylation of Vinylsiloxanes with HydrogensiloxanesA kinetic investigation of the platinum-catalysed hydrosilylation of monofunctional oligomeric vinylsiloxanes by monofunctional oligomeric hydrogensiloxanes was performed under stoichiometric conditions with use of quantitative 1H-NMR spectrometry. The reaction rate up to 50% conversion can be expressed by v=k [Pt]. During further hydrosilylation the kinetic changed to second order. No induction period was observed. A hydrogensiloxane with a dimethylsilyl end group gives much higher rates than a siloxane with a methylsiloxy group. The main reactions of all hydrosilylations, determined by GC-MS and 29Si-NMR, are β-additions. Less then 5% α-products are obtained.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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