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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 6451-6459 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present the results of quasiclassical trajectory (QCT) and quantum centrifugal sudden hyperspherical (CSH) scattering calculations for the Cl+HCl→ClH+Cl reaction using a semiempirical potential energy surface. In particular, we report state-to-state integral and differential cross sections in the vicinity of a transition state resonance that occurs at a total energy E of 0.642 eV. This resonance, which is labeled by the transition state quantum numbers (0,0,2), strongly perturbs the cross sections for the initial rovibrational state HCl(v=1, j=5), which was therefore considered in all our calculations. For E≥0.680 eV, which is well removed from the resonance energy, the QCT and CSH results are in good agreement, but for E near the resonance energy, important quantum effects are found in the integral cross sections, product state distributions, and differential cross sections. The CSH integral cross sections show smooth steplike increases for E≈0.642 eV, which are not seen in the QCT results. Associated with these steps are increased branching to the v'=0 product HCl vibrational state, and a strong propensity for the production of rotational states with j'=15 and 16 for v'=0. These features of the product energy partitioning are not present in the QCT results, although the correct rotational distributions are approximately recovered if the final vibrational action is constrained to match its quantum value. The CSH differential cross sections show a sudden shift from backward to sideward scattering between 0.642 and 0.660 eV, while the QCT cross sections remain backward peaked. An analysis of the "number of atom–diatom encounters,'' during the course of a reactive collision, shows that there are chattering trajectories. These are associated with sideward scattering, but their probability is low and as a result they do not produce distinct features in the angular distributions. However, if the classical deflection function is weighted by the quantum reaction probability, angular distributions are obtained that are in reasonable agreement with the CSH angular distributions (including resonance features).
    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 94 (1991), S. 4311-4319 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An accurate quantum scattering calculation for the Cl+HCl→ClH+Cl reaction has been performed. In particular, we study the influence of the lowest transition state resonance on the energy dependence of the state-to-state integral cross sections and product rovibrational distributions. The calculations use a recently developed centrifugal sudden hyperspherical (CSH) coordinate reactive scattering code. The Bondi–Connor–Manz–Römelt semiempirical potential energy surface is employed. All 161 partial waves needed for the convergence of the cross sections are included in the calculations. We find that the resonance perturbs certain reagent and product rotational levels of the vibrational ground state (v=0, j=14–16), as well as all open rotational levels (j=0–8) of the first vibrationally excited state (v=1). Transitions from the ground reagent to the ground product vibrational state, such as v=0, j=15→v'=0, j '=15, show almost no resonance structure in the integral cross sections; rather direct scattering dominates the partial wave sum. On the other hand, transitions between perturbed v=0 rotational states and any v'=1 rotational state, or between any v=1 state and perturbed v'=0 states, or between any v=1 and any v'=1 state, show a novel resonance feature in the integral cross sections. This novel feature is a sudden smooth "step'' in the integral cross section, centered at the resonance energy for the partial wave with zero total angular momentum quantum number (J=0). The step has a width equal to the J=0 resonance width. Sometimes this step is superimposed on a slowly varying background which arises from direct scattering. A quantitative description of these resonant steps in the integral cross sections is developed using a J-shift approximation. Because the resonance influences all rotational states for v=v'=1 in a similar way, there is no significant effect on the product rotational distributions due to the resonance. However, the resonance does produce detectable stepping behavior in the product vibrational distribution.
    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 103 (1995), S. 5979-5998 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Resonance effects in the differential cross sections of the Cl+HCl(v,j)→ClH(v′,j′)+Cl reaction are analyzed using Regge pole and complex angular momentum (CAM) techniques. This is the first detailed application of CAM theory to reactive molecular scattering. The rovibrational transitions studied are v=1, j=5→v′=0, j′=15, and v=1, j=5→v′=1, j′=5 at total energies E=0.66, 0.68, 0.70 eV. The CAM theory expresses the scattering amplitude as a background subamplitude plus a pole subamplitude. The uniform (and nonuniform) semiclassical evaluation of the background subamplitude is discussed. It is necessary to include explicitly the resonance Regge pole in the semiclassical theory because it has a small imaginary part. We derive a new generic semiclassical formula, involving the complementary error function for the resonance angular scattering. The position and residue of the resonance Regge pole at each E are extracted numerically from scattering matrix elements calculated by the centrifugal sudden hyperspherical (CSH) quantum scattering method. There is good agreement between the semiclassical CAM and CSH angular distributions. However, the latter involve summing a partial wave (PW) series with a large number of numerically significant terms—as a result the PW computations provide no physical insight. We also show that a simple semiclassical optical model becomes inaccurate when the rotational period of the ClHCl complex is comparable to the resonance lifetime. We derive a new "sticky'' optical model which allows for rotation of the complex. All our calculations use the Bondi–Connor–Manz–Römelt semiempirical potential energy surface. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Solid State Communications 89 (1994), S. 475-481 
    ISSN: 0038-1098
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Chemical Physics Letters 206 (1993), S. 119-122 
    ISSN: 0009-2614
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physics Letters A 132 (1988), S. 381-386 
    ISSN: 0375-9601
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Power technology and engineering 3 (1969), S. 847-849 
    ISSN: 1570-1468
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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