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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 108 (1998), S. 6884-6891 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The photochemistry of ozone trapped in solid nitrogen and mixed matrices has been reinvestigated using irradiation at 266 nm and infrared spectroscopy between 10 and 25 K. In this temperature range the most probable reaction channel appears to be the formation of metastable excited nitrous oxide molecules that fragment mostly into an oxygen atom and nitrogen. Recombination of O+O2 is negligible, suggesting that the atomic oxygen that is formed from the deactivation of excited N2O is bound to the nitrogen molecule, preventing the reformation of O3 and leading to a fast first-order photodecomposition of ozone in highly diluted samples. The experimental value of the photokinetic constant suggests that the photodissociation cross section of ozone in matrices at 266 nm is weaker than that measured in the gas phase. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 8636-8642 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The photodissociation of ozone trapped at high dilution in solid argon has been reinvestigated at different temperatures and various photon flux, combining irradiation at 266 nm and infrared spectroscopy. In argon, recombination of O+O2 is a major pathway and the weak decrease of ozone is due to cage exit of oxygen atoms which is dependent of the temperature and of the initial photon flux. Kinetic curves are well fitted by a double exponential expression and a model based upon two different cage exit pathways is proposed. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 4045-4052 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Infrared spectroscopy has been coupled with the matrix isolation technique. First, to identify the ozone dimer isolated in solid argon, and second, to investigate the mechanism of its photodissociation at 11 K using the 266 nm laser line. Identification of dimers, which are trapped in two different sites, was performed through the observation of the ν3 asymmetric stretching modes. By absorption of one photon, dimers are photodissociated with a high photolysis rate when compared with that of ozone monomers, suggesting the absence of cage recombination of the photofragments. Experimental observations suggest that the major pathway after photolysis is the formation of an excited transient species O4*, which fragments into O+O3. A two-step mechanism, involving the subsequent reaction of O(1D) with O3 formed in a first step appears unlikely. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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