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    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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