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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 10 (1977), S. 1307-1315 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 2441-2451 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several dyes have been discovered which sensitize the photolysis of diaryliodonium salts at visible wavelengths. By using the combination of a dye and a diaryliodonium salt, visible light can be used to photoinitiate cationic polymerization. In this article, the dye-sensitized photopolymerizations of cyclohexene oxide, epichlorohydrin, and 2-chloroethyl vinyl ether are described.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3845-3858 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photosensitive polyimidothioethers were prepared by the base-catalyzed condensation of bisthiols with 4,4′-(N-maleimido)diphenyliodonium chloride. Copolymers with other bismaleimide monomers were also prepared. The ultraviolet-induced degradation of two of the copolymers was studied and the effects of light intensity on the rate of photolysis determined. It was also demonstrated that the range of spectral sensitivity of these polymers can be extended into the visible region through the use of dye sensitizers.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    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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  • 5
    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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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1047-1057 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Triarylselenonium salts with complex metal halide anions such as BF4-, AsF6-, and SbF6- have been prepared and have been shown to be efficient photoinitiators of cationic polymerization. The photolysis rates of these compounds were studied and their quantum yields of photolysis were reported. Use of specific triarylselenonium salts in the polymerizations of cyclohexene oxide, epichlorohydrin, and 2-chloroethyl vinyl ether are described.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 2877-2892 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dialkylphenacylsulfonium salts in which the anions are of the general type BF4-, AsF6-, PF6-, and SbF6- are a new class of useful photoinitiators for cationic polymerization. On irradiation these salts underwent reversible ylid formation with the simultaneous generation of strong Brφnsted acids. The photoinitiated cationic polymerization of a number of monomers with dialkylphenacylsulfonium salts demonstrated the utility of these new photoinitiators.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 977-999 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Triarylsulfonium salts Ar3S+MXn- with complex metal halide anions such as BF4-, AsF6-, PF6-, and SbF6- are a new class of highly efficient photoinitiators for cationic polymerization. In this article we describe several synthetic routes to the preparation of these compounds along with their physical and spectroscopic properties. Mechanistic studies have shown that when these compounds are irradiated at wavelengths of 190-365 nm carbon-sulfur bond cleavage occurs to form radical fragments. At the same time the strong Br∅nsted acid HMXn, which is the active initiator of cationic polymerization that takes place in subsequent “dark” steps, is also produced. A study of the parameters that affect the photolysis of triarylsulfonium salts is reported with a measurement of the absolute quantum yields. The cationic polymerizations of four typical monomers - styrene oxide, cyclohexene oxide, tetrahydrofuran, and 2-chloroethyl vinyl ether - with triarylsulfonium salt photoinitiators are described.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1059-1065 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Perylene has been found to photosensitize the photolysis of triarylsulfonium salts at wavelengths from 390 to 475 nm. Using perylene in combination with various triarylsulfonium salt photoinitiators, the photoinduced cationic polymerizations of cyclohexene oxide and 2-chloroethyl vinyl ether have been demonstrated using light of these wavelengths.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    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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