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  • 1
    ISSN: 1011-1344
    Keywords: Candida phototoxicity test. ; DNA reactions ; Pyrrolocoumarins ; laser flash photolysis ; photohaemolysis ; photosensitizers ; phototoxicity
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 1939-1948 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The benzophenone-sensitized solution-phase photocycloaddition polymerization of N,N′-polymethylenebisdichloromaleimides has been investigated. It is shown that a polymer can be obtained by repeated 2π + 2π photocycloaddition process. The intrinsic viscosity of the products varies from 0.1 to 0.6 when the link between the two maleimide moieties contains more than six and simultaneously an uneven number of methylene units. The polymeric materials form transparent, flexible, noninflammable films and decompose at 310°C.
    Additional Material: 2 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 13 (1975), S. 201-213 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The solid-state photoreactivity of a series of maleimides and bismaleimides is studied Various crystalline maleimides are found to dimerize on irradiation by ultraviolet light Based on this discovery, the photopolymerizability of the related bismaleimides in the crystalline state is examined. As a result it is found that some N,N,-alkylenebismaleimides polymerize into highly crystalline polymers. The polymers do not melt below their decomposition temperature (〉300°C) and are practically insoluble in all solvents. The obtained irradiation products are different from the reaction products of the solution-phase photochemistry. Closely related bismaleimides, such as members of a homologous series, show substantial differences in their solid-state photochemical behavior; on excitation they either lead to polymers or are not reactive. This indicates that the solid-state photoreactivity of maleimides and bismaleimides is controlled by the geometry of their crystal structure.
    Additional Material: 3 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 13 (1975), S. 215-225 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the photoreduction of benzophenone and the reductive photopolymerization of diaryl ketones are closely interrelated. The photoreductive polyrecombination presents the characteristics of a polycondensation, namely, an increase in molecular weight with reaction time. In the absence of side reactions, benzophenone and diketone Ia show identical behavior toward hydrogen abstraction, as is reflected in the di-bis rate constants of hydrogen abstraction.
    Additional Material: 6 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 13 (1975), S. 227-252 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The irradiation of nonconjugated bichromophoric systems, diaryl ketones, with ultraviolet light in the presence of hydrogen donors, such as isopropanol or bisbenzhydrol, yields high polymers. Two series of arylketones were investigated, namely bisbenzophenones and bisketotriazoles. The cage reaction, which arises from the cross combination between the acetone ketyl and bisbenzophenone ketyl radicals, was estimated to be very small but may constitute a chain termination reaction in the photopolymerization in isopropanol. The photopolymerization of bisdiketone-dihydrol systems was found to yield polymers with much higher molecular weights than those obtained from the photopolymerization of bisdiketone-isopropanol systems. The photolysis of some binary mixtures of aromatic diketones in the presence of isopropanol yielded statistical copolypinacols. In some favorable cases, the NMR spectrum of the copolymer obtained showed three distinct linkages and from the infrared spectrum intensities the copolymers composition and the number average length of the sequences may be determined.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 1687-1699 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The term, “photopolymerization,” is defined as a polymerization process in which every chain-propagating step involves a photo-chemical reaction. This type of polymerization is exemplified by the unsensitized solution photocyclopolymerization of several N,N ′-alkylenebismaleimides, substituted at the double bond. N,N ′-Alkylenebismaleimides substituted with a bromine atom or two methyl groups at their double bond produce high polymeric products upon ultraviolet irradiation in solution. A general reaction scheme for the photopolymerization is proposed. Kinetic measurements show that the solution photopolymerization of substituted bismaleimides is a multistep reaction.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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