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  • 1
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 8825-8831 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Recurrence relations are derived for constructing rotation matrices between complex spherical harmonics directly as polynomials of the elements of the generating 3×3 rotation matrix, bypassing the intermediary of any parameters such as Euler angles. The connection to the rotation matrices for real spherical harmonics is made explicit. The recurrence formulas furnish a simple, efficient, and numerically stable evaluation procedure for the real and complex representations of the rotation group. The advantages over the Wigner formulas are documented. The results are relevant for directing atomic orbitals as well as multipoles. © 1999 American Institute of Physics.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 2910-2920 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Transformations among molecular orbitals are often expedient or illuminating, and sometimes essential in quantum chemical contexts. In order to express the many-electron wavefunction in terms of the corresponding transformed configurations, full CI calculations used to be repeated in the transformed orbital basis. The configurational transformations can however be obtained directly, as shown by Malmqvist, by a factorization into single orbital transformations. In the present paper, a direct transformation method is presented that is based on the factorization of orbital transformations in terms of Jacobi rotations. Compared to the repetition of a CI calculation, both direct re-expansion methods drastically reduce the computational effort and increase the numerical accuracy. They are, moreover, applicable to wavefunctions whose original construction is not accessible. © 1999 American Institute of Physics.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 4208-4212 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: A global understanding of the geometric phase theorem associated with conical intersections is gained in terms of local properties of the Hamiltonian along the path actually traversed by means of a resolution of adiabatic states in terms of diabatic states. The analysis also answers certain questions that are left open by formulations in terms of intersection seams. It moreover leads to a method for determining the location of the adiabatic intersections. © 1999 American Institute of Physics.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 107 (1997), S. 4307-4317 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The ground and next excited 1A1 potential energy surfaces of the valence-isoelectronic molecules O3, S3, SO2, and S2O have been studied using full-valence-space-multiconfiguration self-consistent-field calculations. An open and a ring minimum were found for all species. In each case, interconversion between the C2v open and closed isomers proceeds via a C2v transition state which lies on a very sharp ridge separating the basins surrounding the minima. In the immediate vicinity of these transition states, the upper state for each species is found to have a minimum, also in C2v. Furthermore, not far away on the C2v ridges, the 1 1A1 and 2 1A1 surfaces intersect conically for all molecules. © 1997 American Institute of Physics.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 6101-6101 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: It is shown that the quadratic steepest descent procedure developed in three previous papers goes smoothly and naturally into a limiting form, presenting no computational problems, when the Hessian becomes singular. This is in contrast to quasi-Newton algorithms which, in the case of singular or near-singular Hessians, yield unrealistic search directions and are kept from breaking down only by introducing arbitrary additional assumptions. The reason is that quasi-Newton algorithms give inadequate weight to the first order variation of the energy, i.e., its gradient.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 2157-2167 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: An analysis is given of the so-called "image function'' approach to finding transition states. It is demonstrated that, in fact, such functions do not exist for general potential energy surfaces so that a plain minimum search is inappropriate. Nonconservative image gradient fields do exist, however, and their field lines, defined by Euler's equation, can lead to transition states as exemplified by quantitative integrations of these equations for the Müller–Brown surface. As do gradient fields, image gradient fields contain streambeds and ridges, but their global structure is considerably more complex than that of gradient fields. In particular, they contain certain singular points where the image gradients change sign without passing through zero. They are the points where the two lowest eigenvalues of the Hessian are degenerate. Some of them can act as singular attractors for the image gradient descent and any algorithm must contain safeguards for avoiding them. (Such regions are equally troublesome for quasi-Newton-type transition-state searches.) Image gradient fields appear to have considerably larger catchment basins around transition states than do quasi-Newton-type or gradient-norm-type transition-state searches. A quantitative quadratic image-gradient-following algorithm is formulated and, through applications to the Müller–Brown surface, shown to be effective in finding transition states.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 1779-1779 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Inorganic chemistry 3 (1964), S. 784-784 
    ISSN: 1520-510X
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 3790-3798 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Using the quantum chemical construction of diabatic states from adiabatic states formulated in the subsequent paper, the lowest two 1A1 states of ozone are expressed in terms of its diabatic components and the interaction matrix Hij between them is determined. An analysis of the electronic structure of the diabatic states leads to an understanding of the reasons for the sign changes in ΔH and H12 and, hence, for the conical intersection between these two low-lying closed-shell adiabatic states of like symmetry.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 5257-5268 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: A novel second-order algorithm is formulated for determining steepest-descent lines on potential energy surfaces. The reaction path is deduced from successive exact steepest-descent lines of local quadratic approximations to the surface. At each step, a distinction is made between three points: the center for the local quadratic Taylor expansion of the surface, the junction of the two adjacent local steepest-descent line approximations, and the predicted approximation to the true steepest-descent line. This flexibility returns a more efficient yield from the calculated information and increases the accuracy of the local quadratic approximations by almost an order of magnitude. In addition, the step size is varied with the curvature and, if desired, can be readjusted by a trust region assessment. Applications to the Gonzalez–Schlegel and the Müller–Brown surfaces show the method to compare favorably with existing methods. Several measures are given for assessing the accuracy achieved without knowledge of the exact steepest-descent line. The optimal evaluation of the predicted gradient and curvature for dynamical applications is discussed.
    Materialart: Digitale Medien
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