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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 67 (1985), S. 63-89 
    ISSN: 1432-2234
    Keywords: Topological-effect-on-molecular-orbitals (TEMO) theorem ; non-empirical HF SCF calculations ; perturbational-variational Rayleigh-Ritz (PV-RR) analysis ; topological molecular models
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Three models for constructing topologically related pairs of molecular isomers are discussed at length. The topological-effect-on-molecular-orbitals (TEMO) theorem is presented in detail and illustrated with experimental data; this theorem demonstrates that molecular topology imposes constraints in the form of general interlacing rules on the MO energy patterns of topologically related molecules. Further, non-empirical SCF MO calculations have been performed for topologically related o- and p-divinylbenzenes, difluorobenzenes, benzoquinones, and benzoquinodimethanes in standard and optimized geometries using various basis sets. In most cases, the SCF π-MO eigenvalue patterns of topological related isomers are in complete agreement with the TEMO theorem, thus demonstrating the dominant influence of topology on the π-MO energies. A modified version of the generalized perturbationalvariational Rayleigh-Ritz (PV-RR) procedure is described which is used to study the occasional observed deviations from the TEMO predictions; this procedure had been combined with the concept of critical λ (i.e. the threshold value of the perturbation parameter λ at which the TEMO order of a pair of MO eigenvalues starts to invert), thus enabling us to analyze in quantitative detail the physical factors which compete with molecular topology in conditioning the ab initio MO energy patterns.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 18 (1980), S. 867-890 
    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 large family of interlocking perturbational inequalities is derived by variational considerations for the stationary states of all systems described by a Hamiltonian linear in a real perturbing parameter λ. These inequalities constrain in many different ways the perturbation expansions of both exact and variational eigenvalues for these systems; analogous inequalities are derived for the components of the eigenvalues. A special feature of the analysis consists of obtaining inequalities applicable to the separate sums of even- and odd-order perturbation energies. For lowest states of each symmetry and for positive definite perturbing operator, the interlocking effect of the inequalities becomes extremely restrictive. The inequalities are illustrated with several numerical calculations for different systems and states of the helium isoelectronic sequence. The direction of the inequalities is found to be unaffected by low-order truncation, thus rendering them applicable to low-order perturbation expansions. The inequalities are used to study the efficacy of low-order perturbation theory for two- to ten-electron atomic isoelectronic sequences, and to determine the functional dependence upon λ of the eigenvalues and their components for arbitrary atomic isoelectronic sequences.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 25 (1984), S. 915-928 
    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: The generalized Hellmann-Feynman and curvature theorems are derived for the generalized Sturm-Liouville-type eigenvalue equation which is widely encountered in many branches of physics. In classical mechanics, the Sturm-Liouville eigenvalue equation primarily arises from applying the theory of small oscillations to vibration problems while, in quantum mechanics, the most important example is the time-independent Schrödinger equation. The generalized theorems, respectively, provide simple useful expressions for the first and second λ derivatives of the eigenvalue where λ is an arbitrary real parameter appearing in the eigenvalue equation. These results, which apply to both classical and quantal systems, include as special cases the well-known quantum mechanical Hellmann-Feynman and curvature theorems for the time-independent Schrödinger equation, thus unifying the formalism. This connection between classical and quantum mechanics is of interest per se, and also because classical eigenvalue equations find application in the treatment of some quantum chemical problems. Two derivations of both generalizations are presented, the first proof applying to exact and Rayleigh-Ritz (linear variational) solutions of the eigenvalue problem, and the second, more general one, to arbitrary optimal variational as well as exact solutions. Necessary and sufficient conditions for the validity of the results are discussed. To demonstrate the insight they afford, several applications of the theorems in conjunction with perturbation theory are described.
    Type of Medium: Electronic Resource
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