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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 3779-3789 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A formulation for calculating frequency-dependent hyperpolarizabilities in the Møller–Plesset perturbation theory is presented as the correlation correction to the TDHF approximation. Our quasienergy derivative (QED) method is applied, and the difference between the QED method and the pseudoenergy derivative (PED) method by Rice and Handy is discussed. The Lagrangian technique is utilized to obtain simple and practical expressions for response properties in which the TDHF orbital rotation parameters satisfy the 2n+1 rule and the Lagrange multipliers satisfy the 2n+2 rule. Explicit expressions for response properties up to third order [μ, α(−ω1;ω1), β(−ωσ;ω1,ω2)] are derived in the second-order Møller-Plesset perturbation theory.
    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 99 (1993), S. 3738-3778 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The higher-order response theory to derive frequency-dependent polarizabilities and hyperpolarizabilities is examined by means of the differentiation of the "quasienergy'' with respect to the strengths of the time-dependent external field, which is referred to as the quasienergy derivative (QED) method. This method is the extension of the energy derivative method to obtain static polarizabilities and hyperpolarizabilities to a time-dependent perturbation problem. The form of the quasienergy W = 〈Φ||Hˆ − i(∂/∂t)||Φ〉 is determined from the time-dependent Hellmann–Feynman theorem. The QED method is accomplished when the total sum of the signed frequencies of the associated field strengths, with respect to which the quasienergy is differentiated, is equated to 0. The QED method is applied to the single exponential-transformation (SET) ansatz (up to the fifth-order QEDs) and the double exponential-transformation (DET) ansatz (up to the fourth-order QEDs), where the time-dependent variational principle (TDVP) is employed to optimize the time development of the system. The SET ansatz covers the full configuration interaction (CI) response and the Hartree–Fock response (i.e., the TDHF approximation), while the DET ansatz covers the multiconfiguration self-consistent field (MCSCF) response (i.e., the TDMCSCF approximation) and the limited CI response with relaxed orbitals. Since the external field treated in this paper is always "polychromatic,'' the response properties explicitly presented for both the SET and DET ansätze are μA, αAB(−ω;ω), βABC(−ωσ;ω1,ω2), and γABCD(−ωσ;ω1,ω2,ω3), in addition δABCDE(−ωσ;ω1,ω2,ω3,ω4) is presented for the SET ansatz. All variational formulas for these response properties derived in this study automatically satisfy the (2n+1) rule with respect to the variational parameters.
    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 111 (1999), S. 2878-2888 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A time-dependent density-functional theory for systems in periodic external potentials in time is formulated on the assumption of the existence of the Floquet states from the quasienergy viewpoint. Coupling strength integration, which connects a noninteracting system with an interacting system, is introduced by using the time-dependent Hellmann–Feynman theorem. Coupled perturbed time-dependent Kohn–Sham equations are derived from the variational condition to the quasienergy functional with respect to parameters. Explicit expressions for frequency-dependent polarizability and first hyperpolarizability are given by the quasienergy derivative method. Excitation energies and transition moments are defined from poles and residues of frequency-dependent polarizabilities, respectively. In contrast to the previous theory, our formulation has the following three advantages: (1) The time-dependent exchange-correlation potential is defined by the functional derivative of the exchange-correlation quasienergy. (2) The formal expression for frequency-dependent polarizability, which corresponds to the exact sumover-states expression, can be obtained. (3) Explicit expressions for response properties which satisfy the 2n+1 rule can be automatically obtained. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We replied to the comment by Banerjee and Harbola on our previous paper [J. Chem. Phys. 111, 2878 (1999)]. As their comment, the basic direction of our previous paper is similar to theirs [Phys. Lett. A 236, 525 (1997) and Eur. Phys. J. D 5, 201 (1999)]. However, there exist the significant differences between them concerning (1) the description of the exchange-correlation quasienergy functional, (2) the universality of the expression of hyperpolarizabilities, (3) the derivation of the expression for the excitation energies and transition moments, and (4) the orbital quasienergy matrix in the coupled-perturbed Kohn–Sham equation. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 51 (1994), S. 87-97 
    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: A formulation for calculating frequency-dependent hyperpolarizabilities in the coupled-cluster (CC) theory with the Brueckner orbitals is presented. Our quasi-energy derivative (QED) method is applied, and explicit expressions for response properties up to third order [μ, α(-ω1;ω1), β(-ωσ;ω1, ω2)] are derived. The position of the resonances is determined from the RPA-like equation. It is found that the pole structures are not compatible with ones of the exact response functions. An extension of the coupled Brillouin-Brueckner CEPA-0 by Kutzelnigg to the time-dependent case is also discussed. © 1994 John Wiley & Sons, Inc.
    Type of Medium: Electronic Resource
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