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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 5751-5752 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Negative ion formation during collisions between Cs (ns,nd) Rydberg atoms and CS2 molecules has been studied for intermediate values of the effective principal quantum number (n*=10–26). Rate constants for CS−2 formation are found to be different for the two isotopes C32S34S and C32S32S for a narrow range of n* near n*=17, with the rate constant for 12C32S34S− production being up to 4.5 times larger than that for 12C32S32S−.
    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 104 (1996), S. 1225-1231 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Using recently measured accurate relative partial ionization cross section functions for production of the C60 fragment ions C+58 through C+44 by electron impact ionization, we have determined the respective binding energies BE(C+n–C2), with n=58,...,44, using a novel self-consistent procedure. Appearance energies were determined from ionization efficiency curves. Binding energies were calculated from the corresponding appearance energies with the help of the finite heat bath theory. Then using these binding energies we calculated with transition state theory (TST), the corresponding breakdown curves, and compared these calculated ones with the ones derived from the measured cross sections. The good agreement between these breakdown curves proves the consistency of this multistep calculation scheme. As the only free parameter in this procedure is the binding energy C+58–C2, we studied the influence of different transition states chosen in the determination of this binding energy via TST theory and iterative comparison with breakdown curve measurements. Based on this study we can conclude that extremely loose transition states can be confidently excluded, and that somewhat looser transition states than those used earlier result in an upward change of the binding energy of less than 10% yielding an upper limit for the binding energy C+58–C2 of approximately 7.6 eV. © 1996 American Institute of 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〉 67 (1963), S. 1615-1617 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 97 (1993), S. 2500-2504 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 97 (1975), S. 2921-2922 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 21 (1991), S. 335-342 
    ISSN: 1434-6079
    Keywords: 36.40.+d ; 34.30.+h
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Two methods are described for obtaining activation energies for evaporation from isolated clusters. They involve measurements of (1) kinetic energy distributions during evaporation and (2) metastable decay probabilities. The two methods supplement each other and can be applied to data garnered in the same apparatus. The methods are illustrated with applications to data in the literature on copper and carbon clusters. An even/odd alternation in evaporation energies from the copper clusters is consistent with a similar alternation in electron affinities, but not with elementary theory. Thermodynamic properties of carbon clusters are also deduced and discussed.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 5 (1987), S. 83-89 
    ISSN: 1434-6079
    Keywords: 36.40+d ; 34.30+h
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract This work is concerned with evaporation from an ill-defined miscellany of isolated aggregates. The evaporative ensemble is accordingly defined and its time-dependent properties developed. Initially this is done using phenomenologically-derived expressions for rates of evaporation. They assume implicitly that the thermodynamic properties of aggregates are continuous functions of their size. Several general properties of unimolecular rate constants are then used to show how local irregularities in these properties will manifest themselves within the ensemble. In particular the Carnot-Kelvin factor is seen to be capable of magnifying the effect of small deviations to discernible magnitudes. This magnification must nevertheless be a decreasing function of time. A concomitant de-evolution of magic-number effects follows inescapably. The manifestation of local deviations in metastable abundances is also investigated, and is illustrated by reference to evaporation from ionic copper clusters.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 20 (1991), S. 105-109 
    ISSN: 1434-6079
    Keywords: 36.40 + d ; 34.30 + h
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Beginning with rather basic principles, general relations are obtained for evaporative rate constants. These are established both as a function of energy and of temperature. In parallel with this, expressions are developed for the kinetic energy distribution of the separating species. Explicit evaluation of the rate constants in the case of “chemical” evaporation from an entity containingn monomeric units yields as a typical result $$k(T)(s^{ - 1} ) = 3 \cdot 10^{13} n^{{2 \mathord{\left/ {\vphantom {2 3}} \right. \kern-\nulldelimiterspace} 3}} \exp [6/n^{{1 \mathord{\left/ {\vphantom {1 3}} \right. \kern-\nulldelimiterspace} 3}} ]\exp ( - \Delta E_a (n)/k_B T)$$ Experimental evidence in support of this relation is cited. Applications to thermionic emission are also noted.
    Type of Medium: Electronic Resource
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