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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 1796-1812 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A theoretical study of the relationship between interatomic distances and the spectral positions of valence- and K-shell σ* photoionization resonances is reported for a selected series of molecules. Three-dimensional graphical representations of the occupied and virtual-valence σ-symmetry orbitals of these compounds reveal their striking similarity to the wave functions of a particle in a cylindrical well, substantiating qualitative notions long employed in free-electron molecular orbital (FEMO) approximations. Accordingly, the molecular potential along the symmetry axis in these compounds is modeled after a finite square well, with a depth approximately equal to the energy of the lowest σ-symmetry valence molecular orbital and a width determined from analogies to FEMO theory. Calculated minimal-basis-set molecular-orbital energies for both occupied and virtual states are seen to correlate accurately with the simple square-well energy level formula (π2 /2)(n2/l 2 ) when measured in Hartree atomic units from the bottom of the well. The calculated σ* orbital energies are furthermore in excellent agreement with experimentally and theoretically determined valence-shell photoionization resonance positions, the latter consequently also satisfying the square-well correlation formula. A similar situation obtains for experimentally and theoretically determined K-shell resonance positions, although energy shifts from minimal-basis values are evident in these cases. These circumstances are clarified quantitatively on basis of Feshbach–Fano considerations, in which minimal-basis-set virtual-valence σ* orbitals play the roles of zeroth-order states subject to modification by interactions with nonresonant background continua. Concluding remarks contrast and compare molecular-orbital and square-well approaches to photoionization resonances with those based on multiple-scattering and barrier models. The present results appear to clarify the origins of recently reported empirical correlations of bond lengths with resonance positions, and help to determine their range of applicability.
    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 95 (1991), S. 3107-3118 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An explicit Hilbert-space formulation of Feshbach–Fano theory is described which is particularly well suited for treating the problem of shape resonances in molecular photoionization. The prepared states of Fano and Cooper are employed to resolve the irreducibly infinite degeneracy of molecular electronic continua that arises from the noncentral nature of molecular (body-frame) potentials. Previously defined L2 Stieltjes states generated employing appropriate test functions are shown to converge to these prepared states, avoiding prior construction of the associated degenerate channel functions. A novel choice of zeroth-order state particularly suitable for applications of the L2 Feshbach–Fano method to molecular shape resonances is introduced and shown to avoid many of the difficulties associated with more conventional treatments employing resonance scattering theory. Specifically, the energy of this zeroth-order state is seen to be a weighted average over the correct photoionization cross section, the associated background cross section is shown to vanish for all energies, and calculations of the associated ρ(E) and q(E) parameters are avoided entirely. Computational applications in the static-exchange approximation to selected valence-shell channels in N2, O2, and N2O illustrate the attributes of the method and provide accurate cross sections in each case. The L2 Feshbach–Fano formalism is seen to provide improved results from precisely the same information—pseudostate energies and oscillator strengths—as is required in the conventional L2 Stieltjes development, with no significant increase in computational effort required.
    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 87 (1987), S. 3299-3303 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Polarized fluorescence from the A 2Πu and b 4Σ−g states of O+2 following photoionization of O2(X 3Σ−g) in the 17–21 eV region has been employed to determine population alignment in the O+2 photoion. The measured A-channel polarization exhibits pronounced structure which correlates well with the known positions of (autoionizing) Rydberg states, whereas polarization signal in the b channel has broad and less prominent features. The measured b-channel polarization values (ranging from −0.02 to −0.05) are consistent with single-channel calculations, while the A-channel polarization measurements (which range from 0 to 0.09) are of opposite sign to the previously reported single-channel calculations. The results of more involved calculations show that this sign reversal in the A channel can be attributed to the presence of intravalent 3Σ−u states which autoionize into the A channel in the near-threshold region.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Computational studies are reported of Stieltjes orbitals for Hilbert-space descriptions of discrete and continuum molecular electronic eigenstates. Particular attention is focused on the identification of N → V π(π → π*) and N → Vσ(σ → σ*) intravalence contributions to photoexcitation and ionization spectra in CO and H2CO molecules. Three-dimensional graphical representations of appropriate Stielties orbitals serve to identify the σ → σ* transitions of Mulliken as photoionization resonances above threshold in these compounds, whereas the corresponding π → π* contributions are spectrally localized as familiar discrete excited states. The development illustrates the nature and properties of Stieltjes orbitals, and demonstrates their utility in studies of both discrete and continuum excitation spectra on a common basis.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 23 (1983), S. 135-146 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methods are reported for construction of closed-form optical potentials that provide useful L2-basis-set approximations to the discrete and continuum Schrödinger states of self-adjoint Hamiltonian operators. The potentials are obtained employing information from a finite (Lanczos) reference space only, but nevertheless correspond to explicit summation over an infinite-dimensional remainder space. Connections are indicated between the Stieltjes-Tchebycheff orbital solutions of the resulting optical-potential Schrödinger problem and previously described corresponding moment-theory approximations to spectral densities and distributions. Use of a Lanczos basis insures that the orbital eigenvalues are generalized Gaussian or Radau quadrature points of the spectral density, and that their (reciprocal) norms provide the associated quadrature weights. Convergence of the orbitals in the limit of high order is obtained to Schrödinger eigenstates of finite norm in the discrete spectral region, and to scattering states of improper (infinite) norm in the essential portion of the spectrum. In finite orders the spatial characteristics of the Stieltjes-Tchebycheff orbitals correspond to spectral averages in the neighborhoods of the quadrature points over the correct Schrödinger states. Explicit closed-form expressions are obtained for the spectral content of individual orbitals in terms of orthogonal polynomials without reference to the correct Schrödinger states. A computational application to regular Coulomb l waves illustrates the nature and convergence of the development.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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