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  • 1985-1989  (25)
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 2917-2922 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 3606-3612 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 92 (1988), S. 3252-3260 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 1813-1823 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A study is made of the vibrational energy levels and the corresponding oscillation dynamics of the clusters Xe4He2, Xe3He2, and I24He. XeHe2 is a representative of the "three ball'' clusters, while I2He is a prototype of the "stick and ball'' systems. The treatment is based on the vibrational self-consistent field (SCF) method, which introduces an approximate separation of the modes involved. Success of the method depends on an adequate choice of the coordinates that are being mutually separated. We use physical arguments, based on mass ratios and potential function considerations, as well as comparative SCF calculations in different coordinate systems, to determine the appropriate modes for each system. Numerically exact results are also obtained by configuration interaction (CI) calculations using a basis of SCF states. The SCF and CI calculations include all modes and employ realistic potentials. Several states that are both rotationally and vibrationally excited are also calculated. The main conclusions are: (1) Hyperspherical coordinates are the best modes for XeHe2; ellipsoidal coordinates are best for I2He. In each case, the "good modes'' SCF gives energies in remarkable agreement with the exact (CI) ones. (2) XeHe2 resembles a quantum liquid drop: Even in the ground state, it is delocalized over and between the (two) classical equilibrium structures. (3) Structural distributions, rather than rigid geometry, are essential for the description of such floppy clusters. The single-mode SCF wave functions offer a highly accurate description of the structural distributions. (4) There is a sequence of bound, excited rotational states of I2He in which the He precesses around the I2 axis. The amplitude of the I2He bending vibrations are very large (θA〈20°), but none of the bound states involves a full rotational motion around the I2 stick (with angular momentum normal to the axis). The SCF method with the "good coordinates'' proposed here is expected to yield results of similar high accuracy for any cluster of the "three balls'' or "stick and ball'' types.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 6557-6557 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 1611-1617 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The photodissociation of isolated Cl2 impurities in a Xe crystal was investigated by molecular dynamics simulations. The calculations were carried out for a photodissociation energy of 3.775 eV, and for several temperatures in the range from 10 to 150 K (the melting point is 162 K). The focus was on the physical mechanisms whereby the product atoms exit from the cage, on the properties of the final sites occupied by the Cl atom, and on the temperature dependence of the processs. The main findings were: (1) exit of a Cl atom from the original reagent cage, when it occurs, is always direct upon photodissociation, and does not involve multiple collisions with the surrounding cage walls. This is in qualitative contrast with the dynamics of cage exit in the case of HI photodissociation in Xe at very low temperatures, found in a previous study. (2) The occurrence of product exit from the cage depends entirely on whether the reagent molecule has been oriented at the direction of a transition state for the exit at the instant of photodissociation. (3) The temperature threshold of Cl exit from the cage is 95 K, and essentially coincides with onset of free rotation for the reagent molecules in the host crystal. (4) The temperature dependence of the probability for cage exit is strongly nonmonotonic: The probability increases as T increases from 95 to 110 K, falls off to 0 around 125 K, then increases again as T approaches melting. (5) At the photodissociation energy used, the only site that the Cl atoms occupy in the new cage is the octahedral interstitial site. Various aspects of reaction dynamics in crystalline solids are discussed in the light of the above results and by their comparison with findings of a previous study on photodissociation of HI in Xe.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 3925-3926 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Exact quantum mechanical and quasiclassical trajectory results for rotationally inelastic N2 -corrugated surface collisions are compared over the energy range 0.01–0.04 eV. It is found that the degeneracy averaged, diffraction summed, rotationally inelastic transition probabilities display quantum oscillations.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 174-183 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The photodissociation of HI impurities in a crystalline Xe host is studied by molecular dynamics simulations. From the calculated trajectories, analyses are given for: The behavior of the HI molecule before dissociation, the motions of the fragments following photon absorption, and the sites and vibration dynamics of the H fragments long after dissociation. The main findings include: (i) The photodissociation yield as a function of temperature is not monotonic (0 at 0 K, 0.2 at 17 K, 0.1 at 35 K). (ii) The nascent H atoms, at early time (∼0.5 ps), exhibit well defined, high frequency (∼900 cm−1) vibrations in the cage. The H trajectories acquire increasingly a random walk character with the progress of time. (iii) H exit from the cage is virtually never direct. (iv) After relaxation to equilibrium, the product H atoms occupy dilated interstitial sites (nearest-neighbor xenons displace by 0.3 and 0.6 A(ring) at the octahedral and tetrahedral interstitial sites, respectively). (v) The H atom dynamically distorts the octahedral site and exhibits three well-separated local vibrational frequencies, corresponding to motions along well-defined axes of the site. (vi) The reagent HI molecular rotations are strongly hindered at low temperatures, and are more aptly described as large amplitude bendings associated with the complex Xe⋅⋅⋅HI. The experimental implications of the above findings and the possible consequences of quantum effects are discussed.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 20-30 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 4483-4491 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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