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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inorganic and organometallic polymers and materials 4 (1994), S. 95-142 
    ISSN: 1572-8870
    Keywords: Poly(organophosphazenes) ; bimolecular reactions ; photochemistry ; photophysics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract In the second part of this review we highlight the bimolecular reactions (hydrogen abstraction, and energy or electron transfer) that take place in the photochemistry of poly(organophosphazenes). Both inter-molecular interactions (i.e. between excited free chromophores and ground state groups attached to the phosphazenes, or between excited phosphazene substituents and external quenchers) and intra-molecular processes (i.e. between excited and ground state groups geminally attached to the same phosphorus or supported to different phosphorus along the polyphosphazene skeleton) are exploited. Suggestions are given on the possible practical application of these reactions in different photochemical domains, e.g. heterogeneous-phase photosensitization, photocrosslinking, photoconductivity, microelectronics, light-induced radical polymerization of vinyl monomers, etc.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inorganic and organometallic polymers and materials 4 (1994), S. 1-29 
    ISSN: 1572-8870
    Keywords: Poly(organophosphazenes) ; monomolecular processes ; photochemistry ; photophysics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract In this review we report an outline of the synthesis, UV-Vis spectral characterization, and light-induced reactivity in monomolecular processes of poly(organophosphazenes). The photoreactivity of phosphazene polymers, both in solution and in solid state, strongly depends on the nature of the chromophore attached to the phosphorus atoms of the inorganic −P=N − backbone. In fact, polyphosphazenes not bearing mobile hydrogen atoms in the side moieties undergo, in the first excited singlet state, homolytic eleavage of the bonds connecting the substituents to the inorganic backbone: free radicals of the substituents and phosphazene macroradicals are formed. Moreover, for polyphosphazenes containing labile hydrogens in the side groups, C–H bond scission takes place with the formation of free hydrogens and radicals located in the phosphazene substituents. From these species degradation or crosslinking of the macromolecules will follow according to the experimental conditions.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inorganic and organometallic polymers and materials 4 (1994), S. 205-236 
    ISSN: 1572-8870
    Keywords: Poly(organophosphazenes) ; photochemistry ; photophysics ; photochromism ; azobenzene ; spiropyran ; light-induced grafting ; photo-stabilizers ; photoinitiators
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract In the third part of this review we report some applicative aspects of poly(organophosphazenes) in photochemical fields. In particular, the possible application of phosphazene polymers that contain azobenzene or spiropyran residues as photochromic macromolecules is outlined; the light-induced grafting of organic, carbon-backboned polymers onto polyphosphazene matrices, as a method of modifying both surface and bulk properties of these materials, is highlighted; and the potential application of cyclophosphazenes as photo-stabilizers for commercial organic polymers or as photoinitiators for radical polymerization of vinyl monomers is described.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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