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  • American Institute of Physics (AIP)  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 8262-8263 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: ClO radicals are detected by a laser-induced fluorescence technique, using the C 2Σ–X 2Π transition with a tunable vacuum ultraviolet laser system. Predissociation in the C 2Σ state is discussed in terms of the fluorescence lifetime and excitation spectra. The vibrational distribution of ClO produced by the reaction between O(1D) and HCl is measured.
    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 103 (1995), S. 4490-4495 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Nascent state-resolved ClO(X 2Π) radicals produced in reactions of O(1D) with HCl, CCl4, CFCl3, CF2Cl2, and CF3Cl have been measured, using vacuum-ultraviolet laser-induced fluorescence of the ClO(C 2Σ−–X 2Π) transition. Rotational temperatures of ClO (X 2Π3/2, v=0 and 1) are 900–1000 K for chlorofluoromethanes and 2050±60 K (v=0) and 1770±180 K (v=1) for HCl. The rotational distribution for the O(1D)+HCl system is interpreted by the orbital-to-rotational angular momentum transfer mechanism. Vibrational level populations of the ClO(v=0–3) products are inverted for CCl4 and chlorofluoromethanes, but not for HCl. Vibrational excitations in the v=0–3 levels are higher for the reactions with the larger available energies. © 1995 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 101 (1994), S. 9610-9618 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Speed and angular relaxation processes induced by collisions with He, Ar, Ne, Xe, N2, and O2 for the velocity of superthermal O(1D) photofragments have been studied by measuring the Doppler profiles of O(1D) as a function of the time delay between photolysis and probe laser pulses. The nascent O(1D) atoms, generated in the photodissociation of O2 by linearly polarized light at 157 nm, have a narrow kinetic energy distribution, centered at 9.8 kcal/mol and a large angular anisotropy. The O(1D) atoms are probed with a tunable vacuum-ultraviolet laser at approximately 115.2 nm. The time evolution of the speed distribution is extracted from the Doppler profiles for each bath gas. The anisotropy parameter distribution as a function of the speed at each time delay is also obtained. The distributions obtained indicate that (a) a collision with He reduces the speed of the O(1D) atom efficiently but only changes slightly the direction of its velocity and (b) a collision with Ne or Ar reduces its speed efficiently and almost randomizes the direction of the O(1D) atom velocity. © 1994 American Institute of Physics.
    Type of Medium: Electronic Resource
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