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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 1610-1623 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Combining the versatility of a guided ion beam (GIB) apparatus with a tunable dye laser system, we have studied in detail the ion–molecule reaction Ar++O2→O+2+Ar at collision energies ranging from 0.04 to 3 eV center of mass (c.m.). The results include integral cross sections and product angular distributions. The extracted kinetic energy distributions provide medium resolution information about the energy partitioning, and are indicative of a significant change of the reaction mechanism between 0.05 and 0.5 eV collision energy. Nascent rovibrational state distributions of metastable O+2(a 4Π) products are obtained from 0.5 to 1.4 eV by photofragmentation. In contrast to what is generally expected from charge transfer processes, a preference for excitation of high rotational states at the expense of vibrational states has been observed. The results are discussed qualitatively on the basis of a diatomics-in-molecules (DIM) surface.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 87 (1987), S. 350-359 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Integral cross sections for the reaction of C+ with hydrogen have been determined as a function of translational and rotational energy. Measurements were made with a guided beam apparatus, using a temperature variable scattering cell or alternatively a nozzle beam and different ortho–para mixtures of H2. The detailed results are in good agreement with statistical phase space calculations provided that the nuclear spins are assumed to be completely decoupled (frozen spin approximation). One consequence of fundamental interest is that H2( j=1) is less reactive than H2( j=0) in the threshold region. Further, the theory predicts an oscillatory structure for the kinetic energy dependence of the reaction cross section which has been observed for the first time. The calculated cross sections are used to predict reliable rate coefficients for H2 in selected rotational ( j=0–7) states. An analytical approximation of these results allows a simple calculation of rate coefficients for nonequilibrium rotational populations as can be found, e.g., in interstellar space.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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