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  • Articles: DFG German National Licenses  (14)
Source
  • Articles: DFG German National Licenses  (14)
Material
Years
  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2697-2714 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complex triarylsulfonium salts bearing the thiophenoxy chromophore have been synthesized. The effects of the position of attachment of the thiophenoxy group on the rate of photolysis and in the photoinitiated cationic polymerization of various monomers have been investigated. Other salts in which the thiophenoxy group has been oxidized to the sulfoxide and the sulfone also were prepared to examine the effects of the oxidation state of the sulfur-bearing chromophore on the efficiencies in photoinitiated cationic polymerization. All complex salts having extended conjugation not impeded through positional isomerization or blocked through oxidation of the thiophenoxy chromophore are more reactive than the corresponding triphenylsulfonium salts in cationic polymerization.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2677-2695 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dilphenyl-4-thiophenoxyphenylsulfonium salts have been found to be more efficient cationic photoinitiators than the highly photoactive triphenylsulfonium salts. The former compounds were identified as by-products produced in the preparation of triphenylsulfonium chloride from benzene, chlorine, sulfur monochloride, and aluminum chloride. Confirmation of the structure was made by NMR and UV spectroscopy as well as by independent synthesis. The photoinitiated cationic polymerization of cyclohexene oxide and other epoxy monomers was carried out to demonstrate the higher efficiency of diphenyl-4-thiophenoxysulfonium hexafluoroarsenate as compared to the corresponding triphenylsulfonium salt.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 539-548 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Strong Brønsted acids are produced on reduction of diaryliodonium salts containing anions of the type BF4-, AsF6-, PF6-, SbF6- by ascorbic acid and its derivatives in the presence of catalytic amounts of copper salts. The cationic polymerizations of cyclohexene oxide, tetrahydrofuran, and s-trioxane were studied using the diaryliodonium salt/ascorbate redox couple.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1021-1034 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On irradiation with ultraviolet light, dialkyl-4-hydroxyphenylsulfonium salts undergo reversible photodissociation and in the process generate ylids and Brønsted acids. When the anions are nonnucleophilic in character, as, for example, BF4-, AsF6-, PF6-, and SbF6-, the strong acid which is produced is capable of initiating cationic polymerization. The polymerization of several monomers was carried out to demonstrate the general applicability of these new photoinitiators.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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