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  • American Institute of Physics (AIP)  (4)
  • 1990-1994  (4)
Publikationsart
Erscheinungszeitraum
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 3973-3980 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Multireference configuration interaction calculations (MRD-CI) were carried out in order to obtain the bending and stretching potential energy curves of several low-lying electronic states of the fluoroformyl radical FCO. The study of interactions between valence and Rydberg states as well as that of the dissociative behavior is included in the investigation.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 3347-3360 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The Cs(7P)+H2→CsH(X 1Σ+)(v‘=0,J‘)+H harpooning reaction has been studied in a crossed-beam experiment, with electronic excitation of Cs atoms and laser-induced fluorescence detection of CsH products performed in a coherent saturation regime. Measurements of reactive cross sections have been achieved as a function of two parameters: The collision energy Ec (0.015≤Ec≤0.15 eV) and the rotational quantum number J‘ of CsH products (0≤J‘≤16, in v‘=0). For Ec=0.09 eV, the total reactive cross sections corresponding to the two 7P fine structure levels of Cs are σ(Cs(7P1/2)+H2)=4.2×10−16 cm2 and σ(Cs(7P3/2)+H2)=10−16 cm2. These cross sections are much smaller than expected for a harpooning reaction. This is interpreted from ab initio potential energy and quantal dynamics calculations which show that the efficiency of the photochemical reaction (Cs atoms in the 7P state) is limited by the quenching processes associated with the underlying potential energy surfaces connected with Cs atoms in the 6S, 6P, 5D, and 7S states. From the present measurements, one deduces that the rate of these quenching processes is larger than 90%. The rotational distributions of products in v‘=0 measured at two collision energies (Ec=0.045 and 0.09 eV) are close to "prior'' statistical distributions, with the same "surprisal.'' The energy dependence of rotationally resolved cross sections (J‘ fixed, Ec variable) confirms the reaction thresholds and shows that there is no potential barrier higher than 0.015 eV on the entrance valley and the exit valley of the reactive system; it is in agreement with the dependence predicted by hemiquantal dynamical calculations performed in the frame of a harpooning model. The uncertainty on the measurement of absolute cross sections is larger than 70%, but of the order of 20% for relative cross sections.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 434-444 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The Cs(7P)+H2→CsH (X 1Σ+) (v‘=0,J‘)+H reaction has been studied in a crossed-beam experiment, with electronic excitation of Cs atoms and laser-induced fluorescence detection of CsH products. The Doppler technique has been applied to determine the center of mass angular scattering probability of CsH products, for all rotational levels between 1 and 14 (in v‘=0) and for various values of the collision energy between 0.03 and 0.13 eV. We have used two complementary arrangements of the analysis laser beam: With a "parallel'' arrangement (the laser beam is along the collision axis), the shape analysis of fluorescence profiles leads directly to the angular scattering probability but experimental constraints limit the range of measurements; with a "perpendicular'' arrangement (the laser beam is perpendicular to the collision plane), fluorescence profiles are symmetrical and "forward'' contributions cannot be separated from "backward'' ones. However, extensive shape analyses have been performed with this perpendicular arrangement, since the direction of scattering was determined earlier by recording several profiles with the parallel arrangement. For the title reaction, it is shown unambiguously that, in the center of mass, CsH products scatter preferentially at small angle, in the forward direction with respect to the Cs initial velocity. The angular scattering probability varies with the collision energy but is independent of the rotational level of the product molecule (thus of its recoil velocity). These results are compatible with the harpooning mechanism which was suggested for the reaction.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 3981-3988 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Results of an ab initio study of the vibrational structure of several electronic spectral systems of FCO are presented. An interpretation of hitherto recorded spectra, as well as a prediction of features of yet unobserved electronic transitions is given. The absorption spectra observed in the uv spectral region are ascribed to the transitions involving the first excited states of 2A' and 2A‘ character. The emission spectrum obtained by Toby and Toby [J. Phys. Chem. 85, 4071 (1981)] is assigned to the transition X 2A'←2 2A‘. Reassignment of some observed vibrational bands is proposed.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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