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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 3121-3132 
    ISSN: 0887-624X
    Keywords: hydrosilation ; epoxy monomers ; trialkoxysilanes ; cationic photopolymerization ; ambifunctional monomers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using rhodium and platinum catalyzed regioselective hydrosilation, a series of α-hydrogen-ω-epoxy silane and siloxane compounds have been prepared in good yields. These intermediates have been further condensed with vinyltrimethoxysilane in subsequent hydrosilation reactions to prepare an interesting new class of ambifunctional monomers containing both epoxy and trimethoxysilane groups. It was further shown that these same compounds could be synthesized by a simplified “one-pot” two-step procedure. An investigation of the simultaneous cationic ring-opening polymerization of the epoxy groups and the acid-catalyzed condensation of the trimethoxysilyl groups was carried out. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2729-2737 
    ISSN: 0887-624X
    Keywords: hydrosilation ; Wilkinson's catalyst ; regioselective hydrosilation ; Si—H functional epoxides ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The discovery that the rhodium-catalyzed hydrosilation of unsaturated epoxides with compounds containing two Si—H functional groups proceeds in a discrete, stepwise fashion, has made possible the synthesis of a series of interesting compounds containing both Si—H and epoxy groups in the same molecule. These compounds can be used both as an interesting new class of epoxy monomers as well as intermediates for the preparation of a wide variety of novel monomers which incorporate epoxide as well as other types of polymerizable functional groups © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 3109-3119 
    ISSN: 0887-624X
    Keywords: hydrosilation ; epoxy monomers ; silicon-epoxy monomers ; ambifunctional epoxy monomers ; photoinitiated cationic polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Silicon-containing epoxide compounds bearing Si — H groups can be readily prepared in high yields by the regioselective rhodium-catalyzed monohydrosilation of α,ω-dihydrogen functional siloxanes and silanes with vinyl epoxides. The remaining Si — H groups in these compounds can be further selectively hydrosilated with unsaturated epoxides to give a series of unique ambifunctional monomers containing two different epoxide groups in the same molecule. The photopolymerization of these monomers has been studied using analytical techniques including real time infrared spectroscopy and differential scanning photocalorimetry. On photopolymerization, the new monomers yield interesting networks. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 683-697 
    ISSN: 0887-624X
    Keywords: hydrosilation ; epoxy monomers ; epoxy functional oligomers ; cationic photopolymerization ; regioselective hydrosilation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several series of multifunctional silicon-containing epoxide monomers and oligomers have been prepared using rhodium catalyzed hydrosilation reactions. Dialkyl and diarylsilanes can be condensed with vinyl epoxides to give high yields of the desired diepoxides while the hydrosilation of alkyl and aryl silanes yields a mixture of di and tri epoxy substituted products. The condensation of αω,—Si—H difunctional compounds with vinyl epoxides can be carried out regioselectively to give α-hydrogen-ω-epoxy intermediates, which can be further reacted with di and tri olefins bearing terminal double bonds to give a series of well characterized epoxy functional oligomers. An investigation of the photoinitiated cationic polymerization of the monomers and oligomers, which were prepared during the course of these studies, was carried out. © 1994 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2563-2572 
    ISSN: 0887-624X
    Keywords: hydrosilation ; Wilkinson's catalyst ; regioselective hydrosilation ; siliconeepoxides ; α,ω-dihydrogen-functional oligopolydimethylsiloxanes ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hydrosilation of α,ω-dihydrogen functional oligopolydimethylsiloxanes with epoxy compounds containing vinyl groups has been found to take place regioselectively in such a manner that compounds can be isolated in high yields in which only one Si—H group has been reacted. Three different α,ω-dihydrogen functional oligopolydimethysiloxanes with different chain lengths were monohydrosilated and the resulting epoxide monomers characterized. The rate of hydrosilation at the first Si—H functional group has been shown to be considerably faster than at the second site and from these kinetic studies, activation energies for each hydrosilation step were calculated. Mechanisms are considered which offer an explantion for these observations. © 1993 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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