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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 107 (1997), S. 4919-4926 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Fragment ions energetically emitted following the perpendicular (ΔΛ=+1) transitions of C 1s→π* of CS2, OCS, and CO2 are observed not only in the perpendicular (90°) direction but also in the parallel (0°) to the linear polarization; that is, ions have a momentum orthogonal to the linear molecule. This arises in the Renner–Teller (RT) vibronic coupling of bending vibrations in the C 1s→ in-plane π* excited state with a bent equilibrium geometry, though the RT splitting between the C 1s→ out-of-plane π* state with a linear geometry and the C 1s→ in-plane π* state is not visible directly due to the lifetime broadening. The 0° ion yield is relatively small in CS2 but is comparable to the 90° yield in CO2; in the latter the peak maximum at 0° is 0.06 eV lower than at 90° and the anisotropy parameter β is heavily dependent on the photon energy. In CO2 a great number of unresolved bending vibrations are coupled. The half-width at half-maximum on the lower energy side of the π* peak is much more sensitive to the RT splitting; 0.08, 0.11, and 0.29 eV for CS2, OCS, and CO2, compared with the full-width at half-maximum, 0.17, 0.39, and 0.64 eV. In CS2 the π* peak and β value are sharp and symmetric, indicating that the zero-point vibrational levels are only involved. In OCS three fine structures observed with separations of 0.21 eV are assigned to the ν3 mode, which is comparable to the stretching mode in CO. © 1997 American Institute of Physics.
    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 102 (1995), S. 7369-7376 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have measured high-resolution angle-resolved ion-yield spectra of the O and N 1s excited N2O molecules (Nt–Nc–O) and investigated them with the help of ab initio quantum chemical calculations. The peak width of the Nc 1s→π* transition is larger than that of the Nt 1s→π* one. This mainly arises from different populations of bending vibrations excited through the Renner–Teller effect, which breaks the degeneracy of the 1s→π* excited states by bending the linear molecule. The angular distribution of fragment ions emitted after the Auger decay is also affected by the Renner–Teller effect. That is, fragment ions significantly lose the information of the Π symmetry of the linear molecule. For the 1s→Rydberg excitations no Renner–Teller effect is observed and the angular distribution is directly related to the Σ and Π symmetries. Furthermore, it is found that the peak intensities of the O and Nt 1s→nsσ Rydberg transitions are unusually large. The N2O molecule has two σ* orbitals, σs*(8σ) and σp*(9σ), below and above the ionization threshold and the 1s→σs* excited states are mixed with the O and Nt 1s–nsσ Rydberg excited states; on the other hand, the Nc 1s→σs* transition is almost dipole-forbidden because of the orbital symmetry. © 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 97 (1992), S. 8842-8849 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: High-resolution electron-yield and "symmetry-resolved'' ion-yield spectra have been measured at the N and O K edges of a 2Π open-shell molecule, NO. Several Rydberg transitions converging to the 3Π and 1Π ionization thresholds are found. The core-to-valence and core-to-Rydberg transitions are interpreted with the help of ab initio self-consistent-field configuration-interaction and frozen-core calculations for the core-excited states with three open shells. It is found that the equivalent-core model (N*O=O2) breaks down in discussing the state ordering of the three N 1s–2pπ* excited states, 2Δ, 2Σ−, and 2Σ+. It is important to consider explicitly the core hole and the exchange repulsion between the core and π* electrons.
    Type of Medium: Electronic Resource
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