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  • 1
    ISSN: 1572-8870
    Schlagwort(e): Poly[bis(4-isopropylphenoxy)0.8 (4-benzoylphenoxy)1.2 phosphazene] ; photochemical behavior ; solution ; solid state ; photo-cross-linking
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The synthesis and photochemical behavior both in solution and in the solid state of poly[bis(4-isopropylphenoxy)0.8 (4-benzoylphenoxy)1.2 phosphazene] is described. The main reaction of this material under illumination with light of a wavelength longer than 340 nm is the intramolecular abstraction of an hydrogen atom by the excited benzophenone substituent from the 4-isopropylphenoxy moiety geminally substituted on the same phosphorus of the phosphazene chain. In this way highly reactive radical species are produced which induce very efficient photo-cross-linking of the phosphazene copolymer and insolubilization. The efficiency of this process in the solid state is examined in view of the potential application of this material as a polyphosphazene-based negative photoresist.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1572-8870
    Schlagwort(e): Poly(organophosphazenes) ; photochemical behavior ; light-induced cross-linking ; poly[bis(methoxyethoxyethoxy)phoshazene] ; benezophenone
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The synthesis of a new, highly photosensitive, phosphazene copolymer containing an almost-equimolecular quantity of benzophenone and methoxyethoxyethoxy substituents is reported in this paper, together with the photochemical behavior of this material when irradiated in film both in oxygen and in an argon atmosphere. It has been detected that the photoreactivity of the phosphazene material strongly depends on the light absorption process by the benzophenone moieties, whose selective excitation predominantly brings about an intramolecular hydrogen abstraction reaction from the ethylene oxide units, thus producing highly reactive phosphazene macroradicals. The coupling reactions of these species results in the complete cross-linking of the polyphosphazene substrate and in its total insolubilization. Moreover, the influence of molecular oxygen on the overall photochemical process of the benzophenone/ethyleneoxide-substituted phosphazene copolymer is investigated. The implications of the light-induced reticulation process in the controlled insolubilization of poly[ bis (methoxyethoxyethoxy)phosphazene] are also discussed.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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