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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 6091-6091 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    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. 6590-6605 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A self-consistent time-dependent unrestricted Hartree–Fock (TDUHF) theory of linear and nonlinear optical properties is presented. Expressions are derived to calculate the elements of the linear polarizability tensor α, the first-hyperpolarizability tensor β, and the second-hyperpolarizability tensor γ, in terms of spin-adapted perturbed density matrices. For the hyperpolarizability tensors, β and γ, expressions are also derived from the lower-order solutions to the TDUHF equations. A novel feature of the present formulation is that it automatically allows for the separation of the contributions to (hyper)polarizability tensors from individual spin. Results obtained from the calculations of α(ωσ;αa) for H, C, N, O, F, Si, P, S, Cl, O2, NO, and OH and of β(−ωσ;ωa,ωb) corresponding to various second-order nonlinear optical processes for NO and OH radicals are presented. The present results for α show excellent agreement with the literature data. The calculated result for β(parallel) in the case of the NO radical is too small and has a different sign in comparison to the published experimental data. For both NO and OH, the β tensor for different second-order nonlinear optical processes show the order: β(−2ω;ω,ω)(approximately-greater-than)β(−ω;0,ω) ≡β(0;ω,−ω)(approximately-greater-than)β(0;0,0). © 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〉 99 (1995), S. 9045-9050 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 70 (1998), S. 771-778 
    ISSN: 0020-7608
    Keywords: electric field effects ; hyperfine interactions ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A recently published theory of electric field effects on electron spin resonance hyperfine couplings [Phys. Ref. Lett. 79, 379, (1997)] is extended to nuclear quadrupole coupling. With the use of the ab initio coupled Hartree-Fock approach and augmented Sadlej basis set, results are obtained for the first-order corrections to the isotropic and anisotropic parts of hyperfine coupling tensor and the electronic part of the electric field gradient tensor for 17O and 2H nuclei in OH radical. The first-order coefficients exhibit a number of interesting features. The calculated results, in general, appear to be insensitive to the bond-centered polarization functions used in the calculation.   © 1998 John Wiley & Sons, Inc. Int J Quant Chem 70: 771-778, 1998
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
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