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  • 1995-1999
  • 1980-1984  (1,365)
  • 1982  (1,365)
  • General Chemistry  (1,159)
  • Atomic, Molecular and Optical Physics  (206)
  • Nuclear reactions
Material
Years
  • 1995-1999
  • 1980-1984  (1,365)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 147-151 
    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: We estimate radii of convergence of the Rayleigh-Schrödinger perturbation expansions for various energy levels of the π-electron model of the benzene molecule, described by the Hubbard Hamiltonian in both weakly and strongly correlated limits. They are determined using a “generalized” Cauchy criterion applied to the numerically determined coefficients of the pertinent expansions.
    Additional Material: 1 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 1-2 
    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
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 27-68 
    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 paper is introduced by a description of the role of divergent series in mathematics and their particular use in quantum mechanics. It is emphasized that there is a formal similarity between divergent series in nonrelativistic quantum mechanics and those series occurring in quantum field theory. It is indicated that studies of divergent series in nonrelativistic quantum mechanics can be helpful in the verification of suminability techniques in quantum field theory. The general problems of the application of perturbation theory to the study of the hydrogen atom in external fields are discussed. It is shown how the problem of the continuous spectrum can be bypassed. Further it is shown that algebraic techniques are very useful for a transparent formulation of perturbation theory. The theory is applied to the study of the hydrogen atom in a magnetic field and in an electric field and also to the study of the hydrogen molecule ion. The results for the hydrogen atom in a magnetic field and the hydrogen molecule ion are discussed in detail and the large order behavior of perturbation terms is compared with analytic formulas. Finally the questions of the summability for the series corresponding to the quartic anharmonic oscillator and the hydrogen atom in a magnetic field are discussed. It is seen that large order perturbation theory can be built into a continued fraction representation of a divergent perturbation series. Numerical results are presented for the two perturbation series mentioned above.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 133-146 
    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: The problem of direct Padé summation of Rayleigh-Schrödinger perturbation coefficients for the H atom Stark effect is discussed in light of the location of the Padé representation of the expected Bender-Wu branch cuts in the complex F (field) plane. The resulting conclusion that such direct summation of the divergent perturbation expansion [for the real part of E(F)] might give suggestive, but certainly not convergent, results is documented. The relationship between the Padé problem of representation of cuts and corresponding problems in L2-discretized scattering theory is pointed out. An alternative Padé expansion with newly placed cuts is proposed which is expected to, and indeed does, have excellent convergence properties for real F. The real and imaginary parts of the Stark broadened and shifted hydrogenic ground state are thus obtained directly from the (real) Rayleigh-Schrödinger perturbation coefficients for a large range of fields indicating the power and simplicity of the method.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 179-190 
    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: We present summary results of a bound-state perturbation theory for a one-space and one-time dimension nonrelativistic spinless (Schrödinger) particle, a relativistic spinless (Klein-Gordon) particle, and a relativistic spin-half (Dirac) particle in central fields due to scalar or fourth-component vector-type interactions for an arbitrary bound state. This is accomplished by the reduction of the wave equations to Ricatti form. This enables a decoupling between the pair of coupled first order differential equations on the large and small component Dirac wave functions or a decoupling of the second order differential equation in the Schrödinger or Klein-Gordon equations. All corrections to the energies and wave functions, including corrections to the positions of the nodes in excited states, are expressed in quadratures in a hierarchial scheme, without the use of either the Green's function or the sum over intermediate states. For the ground states of a Schrödinger particle, it is possible to extend this technique to multidimension in the case where the perturbation is due to noncentral fields, for example, in the problem of a nonrelativistic hydrogen atom in a linear combination of multiple fields.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 209-211 
    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
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 239-250 
    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 molecular theory of phase transitions in fatty acid monolayers at the air/water interface is proposed based on rotational ordering of molecules about their longitudinal axes. The first order statistical mechanical lattice model of Bell, Mingins, and Taylor (BMT) which is an equilibrium diluted Ising model is used to describe the monolayer behavior of some simple aliphatic carboxylic acids. The interaction energy parameters in the BMT model are adjusted to give reasonable agreement with the experimentally observed chain length dependence, and the energies thus obtained are compared with those calculated for interacting aliphatic carboxylic acid dimers by the technique of perturbative configuration interaction using localized orbitals (PCILO). It is concluded that intermolecular rotational ordering due to the anisotropy of the intermolecular potential plays a significant role in simple fatty acid monolayer phase behavior. A possible experimental test of the model is briefly described.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982) 
    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
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 369-398 
    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 superoperator formalism for matrix propagators is reviewed, with special attention to the validity of superoperator resolution of the identity. The equation of motion for the particle-hole propagator is discussed. Decoupling procedures based on inner projections and partitioning are examined showing the desirability of self-consistent approximations. The conditions under which a state can be a vacuum for a given linear manifold of operators are analyzed.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 475-485 
    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 total (elastic and inelastic) intensity of electrons scattered by CO2 was measured in the s range of 1 to 12 Å-1 and compared with the theoretical intensity calculated from the Hartree-Fock molecular wave function and those calculated for the independent-atom-model (IAM) molecule. In the range of s ≲ 4 Å-1 the electron correlation effect on the total scattered intensity was found to be represented by that for the IAM molecule.
    Additional Material: 4 Ill.
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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 557-563 
    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 electronic structures of TTF, TTF1+, and TTF2+ are described by means of an ab initio Hartree-Fock-Slater procedure with a double-zeta STO basis. Electronic and photoemission spectra, bonding, and charge distributions are discussed and compared to experiments and previous calculations.
    Additional Material: 3 Tab.
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 885-897 
    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 reduced local energy EL of Rothstein and co-workers is discussed as a criterion for the local accuracy of approximate wave functions. The behavior of EL for different approximation levels is discussed. It is shown that, for particular classes of wave functions, fluctuations of EL reflect local inaccuracies of the wave function as compared to certain convergence limits. The applicability of this criterion is illustrated with approximate Hartree-Fock wave functions for water and methane.
    Additional Material: 4 Ill.
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 927-935 
    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: Starting from the Hohenberg-Kohn functional we show that when the energy density is given as a function of ρ and ∇ρ, i.e., ξ = ξ(ρ, ∇ρ), the condition ∇ρ · n = 0 (which was found by Bader et al. to define virial fragments), appears as a natural boundary condition for the variation of this functional. We also show that when the energy density includes second order derivatives (∇2ρ) this condition is necessary but not sufficient to guarantee the vanishing of the variation. The implications of these results are discussed in the context of a density functional theory for virial fragments.
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  • 14
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982) 
    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
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 967-991 
    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 method for calculating ab initio electronic excitation energies of molecular crystals, based on a many-electron tight-binding approximation, is described. The method follows Frenkel's model for excitons and allows a many-electron treatment of the band-structure problem of molecular crystals. The case of hole bands is studied in detail and various versions of the method are considered. A computational scheme is proposed, in which approximate correlation corrections to the HFR matrix equations of the one-electron LCMO method are calculated. The main effects contributing to these corrections are the effect of relaxation of a molecular ion, the effect of intramolecular electronic-correlation change, and the effect of polarization of the remaining molecules in a crystal. The method developed in the present paper is applied to calculation of the hole bands of the HCP helium crystal.
    Additional Material: 1 Ill.
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  • 16
    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: An ab initio method for calculating the energies of excess-electron bands in a molecular crystal is developed. These energies represent the electron affinities of a crystal. The present method employs a tight-binding approximation to describe the molecules in a crystal and a set of local functions to describe the excess electron. One- and many-electron formulations of the method are given, the latter takes into account the effect of polarization of all the molecules in the crystal by the excess electron. A scheme for approximate determination of the electronic-correlation corrections to the one-electron bands is developed and applied to calculation of the excess-electron bands in the HCP helium crystal.
    Additional Material: 1 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 1041-1050 
    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 theory by which a wave function may be factorized into conditional and marginal amplitudes is extended to the domain of approximate wave functions. The approximate conditional and marginal factors are well defined, and the marginal factor satisfies a variation principle that is equivalent to a reduced Schrödinger equation having the same form as that derived in the case of exact wave functions. Of the two ways of calculating the effective potential in the reduced Schrödinger equation (which are equivalent in the case of exact wave functions), the integral method is demonstrated to be intrinsically more accurate than the differential method. The variation principle for the marginal amplitude leads to a technique for improving approximate wave functions within a subspace of the whole configuration space. These concepts are illustrated by calculations on the ground state of the helium atom.
    Additional Material: 2 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 1123-1125 
    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
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 217-217 
    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
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 253-263 
    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: On the basis of the Heisenberg equation of motion and the Linderberg-Seamans approximations, useful formulas for, β-resonance integrals in the all-valence NDO-like semiempirical methods have been derived. The case of s, p, d basis sets of atomic orbitals has been considered.
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  • 21
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 293-298 
    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 calculations of long-range interaction energy are often based on multipole expansion. The truncated multipole expansion and interaction energy calculated with it are noninvariant with respect to an arbitrary choice of local coordinate systems. In this paper we show that truncated multipole expansion of form Σk = 1n CkR-k is “numerically” independent on a choice of local coordinate systems, if convergence conditions are satisfied.
    Additional Material: 2 Ill.
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  • 22
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 31-36 
    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 model of vibronic coupling of crude Born-Oppenheimer (CBO) potentials within the scope of the linear variational procedure is presented. First numerical results testing the model are discussed.
    Additional Material: 1 Ill.
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  • 23
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 183-190 
    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: Operator Ω and reaction operator T of Löwdin are studied with a slightly different approach, which leads to a clearer understanding of their nature and brings out the relevance of the conditions for the invertibility of K studied in the preceding work in this series.
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  • 24
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 385-395 
    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 method is formulated for enumerating and constructing isomerization reactions of molecules exhibiting large amplitude nonrigid motions. This method not only enumerates the isomers of nonrigid molecules and the corresponding rigid molecules but also the symmetry species spanned by the equivalent structures whose representative is an isomer. Consequently, using the method of correlating the symmetry species of a group to the symmetry species of its subgroup the splitting patterns of isomers of nonrigid molecule to those of rigid molecule are obtained. This provides an elegant method for both enumerating and constructing reaction graphs. The method is illustrated with examples.
    Additional Material: 3 Ill.
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  • 25
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 429-431 
    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
    Additional Material: 1 Tab.
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  • 26
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 443-443 
    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
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  • 27
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 537-545 
    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: Enzymes are large aperiodic structures and this hinders both ab initio molecular orbital and Bloch-type band theory of calculations. A frontier orbital perturbation theory of catalysis is applied to enzymes. Reasons are given for proposing that the induced-fit conformational changes, essential to enzymatic catalysis, leads to an increase in the electronic eigenvalue density at the active site, enhancing the necessary catalytic orbital perturbation.
    Additional Material: 2 Ill.
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  • 28
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    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 199-215 
    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 procedure is given to derive an explicit charge-transfer contribution from the Murrell-Randic-Williams formula, and to implement it in the framework of an additive procedure for the computation of intermolecular interaction energies, as a sum of electrostatic, repulsion, polarization, dispersion, and charge-transfer terms. Comparisons are performed between the radial and angular dependence of this term in model hydrogen-bonded systems, and that of the charge-transfer term resulting from SCF supermolecule computations. The evolution of the derived term can be matched very satisfactorily to that of an SCF counterpart when the counterpoise correction is taken into account. The underlying features governing the radial and angular evolution of the counterpoise and charge transfer terms are underlined.
    Additional Material: 4 Ill.
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  • 29
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 435-440 
    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
    Additional Material: 2 Ill.
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  • 30
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 441-441 
    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
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  • 31
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 459-484 
    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 generalization of the Hartree-Fock molecular orbital (MO) theory for treating diradical intermediates was explained pictorially by drawing molecular orbitals of diradical species such as ring-opened trimethylene. The generalized MO theory applied to elucidate electronic mechanisms of concerted, ionic, radical, and ion-radical reactions of organic reactants in the ground state. Generalized MO computations revealed the most essential characteristics of these reactions and mutal relationships between the worlds of Woodward-Hoffmann and Hughes-Ingold. Generalized MO studies supported our orbital symmetry, stability and pairing rules for concerted, ionic and radical reactions in the ground state, respectively. An extension of MO treatments to excited states reactions was briefly pointed out in relation to the density and spin correlation functions by the multireference CI wave functions.
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  • 32
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 547-556 
    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 nonplanarity of a peptide unit has been studied by the ab initio method (GAUSSIAN 76) considering both the pyramidal structure of nitrogen and the variation of the ω angle for the N-methyl-acetamide and N-ethyl-acetamide in their cis and trans conformations. Several semiempirical methods have also been used for the sake of completeness of this work. All methods except CNDO and PCILO support a nonpyramidal structure for the nitrogen. The distortions of the planarity of the peptide unit show for both cis and trans conformations of the model compounds a significant asymmetric shift of the minimum on the energy curve for the ω rotation.
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  • 33
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 595-630 
    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: Seventeen different computer experiments are presented and analyzed. In each experiment a three-turn B-DNA double helix fragment interacts with a variable number of water molecules (from 60 to 1200), with a variable number of sodium ions (from 30 to 63), at one or more temperatures (280, 300, 320 K). The experiments are performed with the Monte Carlo method using quantum-mechanically derived potentials. In the analysis of the experiments we partition the water molecules (and the corresponding interactions) as being either bound or in the first solvation shell or in the groove regions relative to DNA; for the former two cases, the number of water molecules and the water interaction energy are reported for selected atoms or groups of atoms. The entire study is condensed into eight tables. The use of these tables is exemplified by considering, in detail, some of the trends emerging from these experiments. The analyses are complemented by graphical representations presented either to elucidate the very complex pattern of hydrogen bonded water molecules, or to show the statistical distributions of the oxygen and hydrogen atoms of the water molecules.
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  • 34
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 1059-1082 
    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 theory is outlined of the nature and origin of drug-induced visual hallucination patterns. It is shown that such patterns correspond to blobs or stripes of visual neo-cortical activity. A neuronal circuit is described that generates such patterns whenever its homogeneous resting state becomes unstable. Such a process is shown to be an example of spontaneous symmetry-breaking, similar to that occurring in electro-weak interactions, and in fluid convection. It is suggested that the neuronal instability is produced by the action of hallucinogens on monoamine secreting brain-stem neurons.
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  • 35
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 1085-1152 
    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: Techniques of diagrammatic spin algebra are employed to derive segment factorization formulas for spin-adapted matrix elements of one- and two-electron excitation operators. The spin-adapted basis is formed by the Yamanouchi-;Kotani geneological coupling method, and therefore constitutes an irreducible basis of the unitary group U(N), as prescribed by Gel'fand and Tsetlin. Several features distinguish this paper from similar work that has recently been published. First, intermediate steps in the derivation of each segment factor are fully documented. Comprehensive tables list the spin diagrams and phases that contribute to the possible segment factors. Second, a special effort has been made to distinguish between those parts of a segment factor that can be ascribed to a spin diagram and those parts which arise from the orbitals. The results of this paper should thus be useful for those who wish to extend diagrammatic spin algebra to evaluation of matrix elements for states built from nonorthogonal orbitals. Third, a novel graphical method has been introduced to keep track of phase changes that are induced by line up permutations of creation and annihilation operators. This technique may be useful for extension of our analysis to higher excitations. The necessary concepts of second quantization and diagrammatic spin algebra are developed in situ, so the present derivation should be accessible to those who have little prior knowledge of such methods.
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  • 36
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    International Journal of Quantum Chemistry 22 (1982), S. 1221-1247 
    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 correlation of the K-region carcinogenicity indices of Pullman and of Mainster and Memory with bay-region carbocation delocalization energy (BCDE) is displayed and shown to be maintained at the perturbational molecular orbital (PMO) level. PMO algebraic relations are examined to reveal the underlying relationships. Some correlation between BCDE and K-region indices exists simply because carbocation formation occurs preferentially on carbons which are bonded to positions α (adjacent) to ring fusion centers. Sampling a K region is synonymous with sampling such α carbons. However PMO analysis shows that a very strong correlation exists between BCDE and indices for a certain type of K region (called “primitive”). It is further shown that high BCDE is favored by a straight-line chain of benzene rings as one moves away from the bay region. Kinks in the chain will lower the BCDE, and the closer the kink is to the bay region, the greater is its effect. Effects of methylation upon BCDE are shown to correlate with K-region indices if the methylation occurs at a carbon which is in the opposite class as the carbon to which the bay-region carbocation is attached.
    Additional Material: 19 Ill.
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  • 37
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    International Journal of Quantum Chemistry 21 (1982), S. 69-92 
    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: Instead of the Schródinger equation HΨ = EΨ subject to the boundary condition 〈ϕ|Ψ〉 = 1, where ϕ is a normalized reference function in the Hilbert space, one studies the inhomogeneous equation (H - E)ΨE = aϕ, where E is a complex variable, with the same boundary condition, which gives a = 〈ϕ|H|ΨE〉 - E = E1 - E. Introducing the projector P = 1 - |ϕ〉〈ϕ| for the complement to O = |ϕ〉〈ϕ|, one finds easily the explicit solution ΨE = (1 - PH/E)-1ϕ = (1 + TEH)ϕ, where TE = (E - PH)-1P = P(E - PHP)-1P is the reduced resolvent associated with the auxiliary Hamiltonian H̄ = PHP. The existence of these operators is discussed. It is shown that, if the parameter E is real in the “discrete part” of the spectrum to H, then E and E1 = 〈ϕ|H|ΨE〉 = 〈ϕ|H + HTEH|Φ〉 ≡f(E) bracket a true eigenvalue E satisfying the relation E = f(E). The Newton-Raphson solution to the equation F(E) = E - f(E) = 0 is related to the variation principle. Putting H = H0 + V and expanding the inverse (E - PH0 - PV)-1 in terms of powers of V or (V - α), one gets various expansions relating to finite-order perturbation theory. Exact expressions for the ordinary wave and reaction operators are obtained. If A is an arbitrary nonsingular operator and h = {h1,h2,…,hn} is a linearly independent set, the inner projection Án = |h〉 〈h|A-1|h〉-1〈h| is a “rational approximation” to the operator A which converges toward A when n→∞ and the set h becomes complete. If A is positive (or has a finite negative part) the convergence is from below. Applying this principle to the partitioning technique, one gets rational perturbation approximations instead of the standard power series, similar to the Padé approximants but derived in a different way with the remainder term under control. The method has been used to calculate lower bounds to eigenvalues.
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  • 38
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    International Journal of Quantum Chemistry 21 (1982), S. 125-131 
    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 wave function for hydrogen in the Stark effect (or for the negatively anharmonic oscillator) with an outgoing-wave boundary condition, constructed in Langer-Cherry fJWKB form, is continued back to the origin. The asymptotic expansions for ReE and ImE are determined by the requirement that the wave function be regular at the origin to zeroth and first order in the exponentially small parameter that characterizes ImE. One fJWKB function turns out to be the Rayleigh-Schrödinger perturbation theory wave function.
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  • 39
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    International Journal of Quantum Chemistry 21 (1982), S. 173-177 
    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: It is shown that the renormalization group imposes severe restrictions on analytic continuation in coupling constant in the case of field theories in four dimensions.
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  • 40
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    International Journal of Quantum Chemistry 21 (1982), S. 215-215 
    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
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  • 41
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    International Journal of Quantum Chemistry 21 (1982), S. 251-258 
    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 practical scheme for the calculation of excited states of the same symmetry as a given reference state is outlined in the context of the Hartree-Fock method. In order to prevent the excited state from “collapsing” into a lower-lying state, the prediagonalized Fock matrix is diagonalized in a restricted subspace, deleting the component associated with the orbital which participates in the excitation. Computationally, the deletion is accomplished by means of a “big shift” of the associated diagonal element of the prediagonalized Fock matrix. The resulting wave function will not be fully relaxed, but can be shown to be orthogonal to the reference state. The method has been implemented in a molecular UHF program. Applications to the 4σg-1 hole state of CO and to an excited state of the CuCl42- ion are reported.
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  • 42
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    International Journal of Quantum Chemistry 21 (1982), S. 357-357 
    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
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  • 43
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    International Journal of Quantum Chemistry 21 (1982), S. 399-410 
    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: Using the variational principle, equations have been obtained for density matrix of molecules with the external perturbation of the common type present. The perturbed wave function was taken as a superposition of the ground and single-excited configurations made of the Hartree-Fock molecular spin orbitals. On the basis of these equations a series of variants of static perturbation theory have been worked out for the ground and excited states of closed-shell molecules.
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  • 44
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    International Journal of Quantum Chemistry 21 (1982), S. 465-473 
    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: CI calculations were performed on the energies and relative intensities of the outer and inner valence levels of the CS molecule. Breakdown of the one-particle model is discussed in terms of CI, and the results are compared with the analogous investigations using the Green's function technique.
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  • 45
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    International Journal of Quantum Chemistry 21 (1982), S. 565-579 
    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: We have employed an effective potential and a single-zeta basis in SCF-MO computations to estimate the relative stability of linear disilyne HSiSiH and five isomeric structures defined in earlier all-electron ab initio SCF-MO computations. The effect of electron correlation has been estimated by generalized valence-bond (GVB) computations for the five valence electron pairs of these structures. All our computations indicate that linear disilyne is the least stable structure and that H2SiSi, the silicon analog of vinylidene carbene, is the most stable structure. In these structures silicon occurs in divalent and tetravalent states. The nature of silicon bonding in these valence states is illustrated by contour diagrams of the GVB orbital pairs.
    Additional Material: 6 Ill.
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  • 46
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    International Journal of Quantum Chemistry 21 (1982), S. 581-590 
    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 method is developed for obtaining the spectra of trees of NMR and chemical interests. The characteristic polynomials of branched trees can be obtained in terms of the characteristic polynomials of unbranched trees and branches by pruning the tree at the joints. The unbranched trees can also be broken down further till we obtain a tree containing just two vertices. This effectively reduces the order of the secular determinant of the tree we started with to determinants of orders atmost equal to the number of vertices in the branch containing the largest number of vertices. An illustrative example of a NMR graph is given for which the 22 × 22 secular determinant is reduced to determinants of orders atmost 4 × 4 in just the second step of the algorithm. The tree pruning algorithm can be applied even to trees with no symmetry elements and such a factoring can be achieved. Methods developed here can be elegantly used to find if two trees are cospectral and to construct cospectral trees.
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  • 47
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    International Journal of Quantum Chemistry 21 (1982), S. 633-645 
    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: An effective Hamiltonian for open-shell molecular systems is constructed. The unrestricted Hartree-Fock orbitals are applied as a basis set of one-particle functions. This effective Hamiltonian is determined as a simple product of the original total Hamiltonian and the spin annihilator. The second-quantization formalism and the Feynman-Goldstone diagrammatic technique are used. The resulting effective hamiltonian is composed of zero- to four-particle terms. A possibility of applying the nondegenerate diagrammatic perturbation theory constructed over this effective Hamiltonian is discussed.
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  • 48
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    International Journal of Quantum Chemistry 21 (1982), S. 673-676 
    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 energy of a linearly perturbed enclosed system is calculated by way of the hypervirial methodology in the semiclassical limit. Solutions of this equation are compared with the exact as well as with WKB approximate results for the harmonic oscillator model.
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  • 49
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    International Journal of Quantum Chemistry 21 (1982), S. 717-726 
    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: How the monotonic trend on which the periodicity of the periodic system is superposed is well described by Thomas-Fermi theory is explained. The mathematical structure of the periodicity is elucidated and explained. Algebraic formulas for the key atomic numbers are derived, e.g., the atomic number at which l electrons first appear is given by Zf(l) = 4 (∑n=0l n2)+1.
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  • 50
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    International Journal of Quantum Chemistry 21 (1982), S. 753-765 
    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: We derive basic integrals needed for calculation of matrix elements of the Fourier transformed Coulomb operator and the Fourier transformed square of the Coulomb operator between 1s Slater functions. These integrals arise, for example, in the momentum space (k space) susceptibility formulation of van der Waals forces. The advantages of integration in k space (rather than r space) are that in k space there is a drastic reduction in the number of integration variables, and contour integration can be used. The derivation is completely analytic and the auxiliary integrals are all obtained in closed form.
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  • 51
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    International Journal of Quantum Chemistry 21 (1982), S. 799-811 
    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: Uniform quality basis sets (UQ-NG; N=3, 4, 5), with s = p and s ≠ p, and a 6-31 G* basis set have been optimized for the sulfur atom. These uniform quality basis sets in their uncontracted and contracted forms were used, together with other basis sets reported in the literature (a total of 40 basis sets), to study their accuracy in predicting the bond length and bond angle of H2S.
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  • 52
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    International Journal of Quantum Chemistry 21 (1982), S. 845-849 
    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: Relaxed orbital binding energies of electrons in zinc and cadmium are calculated using a relativistic local density functional theory. The discrepancy between our calculated binding energies and those from gas phase experimental data are attributed to inhomogeniety and many body effects.
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  • 53
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    International Journal of Quantum Chemistry 21 (1982), S. 861-874 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An analysis of the electronic correlation structures by means of the charge and spin correlation functions is carried out for full CI wave functions of four, five, and six membered conjugated π systems described by the Pariser-Parr-Pople Hamiltonian. The low-lying states of these systems are classified as covalent (CV) and ionic (IN) states depending on whether the probability of finding two electrons simultaneously at the same position is small or large. It is found that many of excited CV states, the typical ones of which are the 21Ag state of linear π systems, have stronger CV character than the ground CV state, and their spin coupling structures are different from each other as well as from that of the ground CV state. The spin coupling structure in the ground CV state has an “antiferromagnetic” spin arrangement in favor of antiparallel coupling between nearest neighbor spins while in excited CV states the extent of the antiparallel spin coupling between nearest neighbor sites is decreased. IN states, which are less common for low-lying states than CV ones, are also found to have characteristic modulations in the charge correlation. In particular, the charge correlations in the lowest singlet IN states, 11Bu of linear π systems, 11B2g of cyclobutadiene and 11B1U of benzene, are alternating.
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  • 54
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    International Journal of Quantum Chemistry 21 (1982), S. 875-884 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New formal results regarding the hypervirial analysis of enclosed systems are given. Novel applications are presented and several previous equations are reformulated in a more appropriate form.
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  • 55
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    International Journal of Quantum Chemistry 21 (1982), S. 917-926 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown how the cluster CPA can be used to obtain the local density of states p(E) in a half-infinite or infinite random polymer chain. Calculations were performed for p(E) in a system composed of two coupled random chains with nearest neighbors interaction.
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  • 56
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    International Journal of Quantum Chemistry 21 (1982), S. 941-941 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 57
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    International Journal of Quantum Chemistry 21 (1982), S. 939-940 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 58
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    International Journal of Quantum Chemistry 21 (1982), S. 1003-1017 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A systematic permutation-group approach for both the classification and description of the Feynman-Goldstone diagrams is presented. It allows us to “algebraize” the topological concepts and notions of many-body diagrammatic techniques, for example, the connectivity and disconnectivity of diagrams, the automorphism of a diagram, etc.
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  • 59
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    International Journal of Quantum Chemistry 21 (1982), S. 1029-1040 
    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: In the active site of lactate dehydrogenase important roles are given to aminoacids His195 and Arg171. The coenzyme nicotinamide adenine dinucleotide (NAD) is required in oxidized form (NAD+) for the enzymatic oxidation of the substrate L-lactate. Molecular orbital methods CNDO/2, INDO, and EHT were applied to the study of the model of active center of lactate dehydrogenase. An energetically preferred arrangement of the models of His195, Arg171, NAD+, and lactate was found. Possible biochemical aspects of these arrangements are discussed.
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    International Journal of Quantum Chemistry 21 (1982), S. 1061-1078 
    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 system of time-dependent Hartree-Fock equations allowing the calculation the of nth harmonic generation is established by using the same method used in a former paper in the same conditions. These equations are still subjected to orthonormalization conditions. Then by using a recurrence method, we express these equations in matrix form, as well as the orthonormalization conditions; and, as in the former paper, we then replace the solution of the matrix equation subjected to a constraint by that of a free equation. Finally the elimination of the spin variables allows a further simplification. So we obtain an equation allowing the calculation of the nth harmonic generation.
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  • 61
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    International Journal of Quantum Chemistry 21 (1982), S. 1105-1115 
    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 INDO-SCF method is used to provide electronic indices which are used as independent variables. These attempt to account for the variation in the antitumor activity and toxicity observed within a series of analogs of cis-diamino dichloro platinum(II).
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  • 62
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The formalism for a configuration interaction approach is presented, in which explicit introduction of interelectronic coordinates into individual configurations is accomplished through the use of spherical Gaussian correlation factors. Formulas for all required matrix elements over these configurations are derived, and a computationally convenient algorithm to evaluate the matrix elements is presented. In addition, analysis of the form of the correlation factor shows that both angular and radial correlation can be obtained using spherical Gaussian correlation factors.
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  • 63
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Theoretical computations are performed with the stacking interactions of the 2-naphthylnitrenium ion, the ultimate metabolite of 2-naphthylamine and N-hydroxy-2-naphthylamine, with guanine and adenine. The most stable stacked complex of guanine with this compound is found to be distinctly more stable than that of adenine. The optimized stacking interaction of guanine with 1-naphthylnitrenium ion yields an energy close to that with 2-naphthylnitrenium. By contrast, the dinucleoside monophosphate cytidyl-(3′-5′)-guanosine held in two preselected intercalated conformations is seen to favor 2-naphthylnitrenium over 1-naphthylnitrenium by a significant amount of energy. The possible relevance of this finding to explain the difference in adduct formation with guanine in DNA by the isomeric naphthylnitrenium ions is discussed.
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  • 64
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    International Journal of Quantum Chemistry 22 (1982), S. 101-114 
    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: Electronic energy level set topologies in the abstract nuclear charge space Z of molecular systems are defined and analyzed. Two theorems, one on the general convexity of level sets in Z, another on homotopies of boundaries of level sets, induced by nuclear geometry variations in the nuclear configuration space R, are proven. The applications of the two theorems are illustrated by examples of various molecules and ions.
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    International Journal of Quantum Chemistry 22 (1982), S. 149-168 
    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 general extended geminal model is reviewed and two new approximate models EXGEM2 and EXGEM3 are introduced. In a test calculation on water using a double-zeta basis set, the approximate models recover 93.4% of the full CI correlation energy defined within the same basis set. A test calculation on the neon atom demonstrates that the performance of the models in comparison with the full CI, will improve as the basis set is increased. It is suggested that for basis sets of moderate and large size, and which include polarization functions, the extended geminal models are likely to recover 95%-97% of the correlation energy obtainable by the full CI.
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    International Journal of Quantum Chemistry 22 (1982), S. 219-219 
    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
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  • 67
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    International Journal of Quantum Chemistry 22 (1982), S. 223-239 
    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 complete list of expressions is given covering all possible types of nontrivial two-body operator matrix elements in the unitary group approach. The matrix elements are expressed in terms of factors which depend on the unique spin coupling chain indicated by each Weyl tableau. The method applies equally to pure and mixed orbital configurations. The results extend and clarify previous general treatments of Drake and Schlesinger and Paldus and Boyle. We worked out two examples of 3(ƒ4) matrix elements of V4. V4 interaction and of 4(ƒ5)→4([2(ƒ3)]d2) matrix elements of V1 · V1 interaction.
    Additional Material: 3 Ill.
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  • 68
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    International Journal of Quantum Chemistry 22 (1982), S. 275-288 
    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: We present the first application of the coordinate rotation method, within the time-dependent Hartree-Fock framework, to calculation of positions and widths of metastable excited states. The method is briefly outlined and results of its application to 1P excited states of Li- are given. Comparison of our results to those obtained using electron scattering methods by other workers is also made.
    Additional Material: 3 Ill.
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  • 69
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    International Journal of Quantum Chemistry 22 (1982), S. 331-350 
    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 complete permutational analysis of the XeF6 dynamics is presented. The Longuet-Higgins group for each mode of rearrangement is obtained. On the basis of the splitting scheme of rigid molecule levels and statistical weights and selection rules for the non rigid molecule levels, it appears that transverse digonal twists and turnstile mechanisms have the same spectroscopic effects as the BPR-6 mechanisms. Hence, the previous interpretation of IR and Raman spectra is consistent with tunneling through transverse digonal twists and turnstile mechanisms as well as through BPR-6.
    Additional Material: 6 Ill.
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  • 70
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    International Journal of Quantum Chemistry 22 (1982), S. 397-414 
    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: We show that spin projected unrestricted-Hartree-Fock (PUHF) wave functions are able to well approximate some low-lying covalent states of ring π systems. The UHF wave functions belong to either the axial or torsional spin density wave class. Their spin structures are found to be approximations for the spin correlation structures of the corresponding exact wave functions. The PUHF wave functions become close to exact eigenstates with homopolar valence bond characters in the strong correlation limit.
    Additional Material: 2 Ill.
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  • 71
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    International Journal of Quantum Chemistry 22 (1982), S. 433-434 
    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
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  • 72
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    International Journal of Quantum Chemistry 22 (1982) 
    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
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  • 73
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    International Journal of Quantum Chemistry 22 (1982), S. 485-496 
    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 detailed consideration of the kinetic aspect of the bridge process has allowed us to correctly write a kinetic equation beginning with knowledge of system microparameters. The solution of the equations makes it possible to elucidate the character of the relaxation process and to determine its typical constants as functions of those microparameters. Particular attention was given to kinetics in the presence of polaron effects. In this case the standard perturbation theory applied to derive the kinetic equations is not valid. The solutions obtained for this case are different both in the form of correlation functions and in the character of the interaction taken into account.
    Additional Material: 1 Ill.
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  • 74
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    International Journal of Quantum Chemistry 22 (1982), S. 557-573 
    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: Addition and subtraction operators defined on some subspaces of the full CI space are introduced. It is shown that the effect of these operators on Löwdin many-electron wave functions consists in adding or removing an electron without destroying spin symmetry. Upward and downward recurrence relations for the Sanibel-type coefficients are presented. A strategy for employing the Löwdin functions for the matrix element evaluation and some special decomposition of the fermion creation-annihilation operators are discussed.
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  • 75
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    International Journal of Quantum Chemistry 22 (1982), S. 631-637 
    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: Several configurations of the C2H4 · HF molecular complex were studied using the 4-31G basis set. The most stable configuration was found to be the π hydrogen bonded complex. For this structure the interaction energy was computed employing a double-zeta basis plus polarization functions. The changes in electronic properties of the components C2H4 and HF due to complex formation were discussed.
    Additional Material: 3 Ill.
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  • 76
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    International Journal of Quantum Chemistry 22 (1982), S. 639-647 
    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: Ab initio molecular orbital calculations with an STO-3G basis have been performed to investigate the energetics and electronic properties of some 5-substituted uracils and their 4-OH tautomer forms with R including F, CH3, and OMe. In all cases, the diketo form is more stable. An excellent linear correlation between the calculated and experimental ionization potentials was found.
    Additional Material: 2 Ill.
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  • 77
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    International Journal of Quantum Chemistry 22 (1982), S. 663-663 
    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
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  • 78
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    International Journal of Quantum Chemistry 22 (1982), S. 709-716 
    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: In an attempt to account for the preferential binding to nonactin of K+ relative to Na+, theoretical computations are performed using the intermolecular interaction energies of the ionophore with the two cations. Both K+ and Na+ liganding conformations are considered, and an evaluation is made of the intramolecular energy expenditure caused by the reduction of the size of the cavity. The energy balance for the complexation of the two cations computed by taking into account the cation-ionophore interactions, the interactions between the liganding groups, as well as the desolvation enthalpies of the cations in methanol, favors K+ over Na+ by 4 to 5 kcal/mol, in fair agreement with the difference in the measured enthalpies of binding. The binding of NH4+ to nonactin is also investigated.
    Additional Material: 3 Ill.
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  • 79
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    International Journal of Quantum Chemistry 22 (1982), S. 691-707 
    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: Maps of electrostatic potential around a number of halocarbon anethetics have been obtained through Gaussian ab initio calculations. Information is obtained on the mode of association of these compounds with possible receptors. The positive potential found along the extension of the C—H bonds substantiates the role of the “acidic hydrogen.” The presence of fluorines on the carbon atom to which it is bound restricts the access to this positive site through the repulsive action of the fluorine lone pairs, an observation that explains the very different behavior of chloroform and fluoroform, for example, with respect to their anesthetic potencies and hydrogen bonding abilities. In the absence of an acidic hydrogen the chlorine atoms can serve as associative sites.
    Additional Material: 5 Ill.
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  • 80
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    International Journal of Quantum Chemistry 22 (1982), S. 739-752 
    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 adsorption of one or many silver atoms on a (111) silicon face (reduced to 61 dangling atomic orbitals) is investigated by means of a self-consistent Hartree-Fock method parametrized from atomic and thermodynamical data. The valley sites (above three Si atoms) are favored over the top sites (above one Si atom). The extrapolation of the results obtained for several structures corresponding to the adsorption of n = 1, 2, 3, 4, 6, and 7 Ag atoms allows us to conclude that the most stable structures correspond: for \documentclass{article}\pagestyle{empty}\begin{document}$ \theta = \frac{1}{3} $\end{document} to linear Ag chains (3 × 1 phase), for \documentclass{article}\pagestyle{empty}\begin{document}$ \theta = \frac{2}{3} $\end{document} to an honeycomb lattice (\documentclass{article}\pagestyle{empty}\begin{document}$ \sqrt 3 \times \sqrt 3 $\end{document} phase), and for θ = 1 to a centred hexagonal lattice (\documentclass{article}\pagestyle{empty}\begin{document}$ \sqrt 3 \times \sqrt 3 $\end{document} phase), the Ag atoms located at the centers of the hexagons being beneath the plan of the hexagons. The adsorption energies corresponding to the various θ are practically equal (ca. 3 eV/Ag). The net charges of Ag atoms are equal to 0.35.
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  • 81
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    International Journal of Quantum Chemistry 22 (1982), S. 837-849 
    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 energies of the five lowest 4S and 4P0 states for three-electron ions for 3≤Z≤10 have been calculated by the Hylleraas method. The largest basis set used contained 97 terms with odd as well as even powers of rij. The change of scale r′ = Zr was applied to the Hamiltonian so that the same basis sets could be used for all the three-electron ions leading to great savings in computing time.
    Additional Material: 4 Ill.
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  • 82
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    International Journal of Quantum Chemistry 22 (1982), S. 889-902 
    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: Formulas are presented for the evaluation of the second-order reduced density matrix for correlated wave functions, including wave functions constructed from pairwise nonorthogonal orbitals. Numerical results are provided for the correlation holes and conditional nuclear spin densities for the water molecule.
    Additional Material: 4 Ill.
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  • 83
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When a multilevel system excited by a laser pulse absorbs a cascade of photons, a second pulse of same frequency, equal duration but dephased by π takes it back to its initial state. This property can be inferred by studying the laser field system interaction matrix, using the rotating wave approximation.
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  • 84
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    International Journal of Quantum Chemistry 22 (1982), S. 1033-1036 
    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 simple and straightforward derivation of (in)stability conditions for projected Hartree-Fock solutions is carried out and compared to the existing approaches to the problem.
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  • 85
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    International Journal of Quantum Chemistry 22 (1982) 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 86
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    International Journal of Quantum Chemistry 22 (1982), S. 1083-1084 
    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
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  • 87
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    International Journal of Quantum Chemistry 22 (1982), S. 1189-1207 
    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 formalism has been developed to treat hydrogen-bonded A - H…B systems within the CNDO/2 and the MINDO/3 methodologies. In this formalism the interactions are divided into three distinct classes; those between (a) two hydrogen-bonded atoms, (b) one hydrogen-bonded and non-hydrogen-bonded atom, and (c) two non-hydrogen-bonded atoms. The last class of interactions is treated solely by the existing CNDO/2 or MINDO/3 method. For A -H…B systems, the core resonance integrals are individually parametrized depending upon the class of the interaction. Three types of A - H…B systems have been thus far parametrized. Nine hydrogen-bonded dimers have been studied using the new formalism and the current CNDO/2 and the MINDO/3 methods. MINDO/3 predicts very large interatomic (A -B) distances for the equilibrium geometry, and relatively small stabilization values for the hydrogen-bond energies. CNDO/2 predicts the reverse. The new formalism for both CNDO/2 and MINDO/3 predicts accurate geometries as well as energies for all nine dimers. The new formalisms are called CNDO/2H and MINDO/3H. A general discussion of the nature of hydrogen bonding as exhibited by CNDO/2H and MINDO/3H is presented.
    Additional Material: 12 Ill.
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  • 88
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    International Journal of Quantum Chemistry 22 (1982), S. 1249-1262 
    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 virial theorem has played an important role in applying quantum mechanics to chemical problems. It has served as one criterion of a satisfactory wave function and its consequences on chemical bonding, molecular structure, and substituent effects have been analyzed extensively. A common method of gaining compliance with the virial theorem is to introduce a “scale” factor which adjusts all distances by a factor η. Optimizing the scale factor through the variational principle produces a wave function satisfying the virial theorem. In the present paper it is shown that when this “scaling” procedure is applied to self-consistent wave functions, the virial theorem can be satisfied, but self-consistency is lost. Scaling generally has a small effect on the total energy, but the effects on the energy components (T, Vne, Vee, Vnn) can be two to three orders of magnitude larger and in the range of tens to hundreds of kcal. Consequently, for applications where the energy components are useful, it is highly desirable to obtain wave functions which satisfy the virial theorem and are self-consistent. In the present paper, a simple, inexpensive extrapolation technique is reported which requires one integral evaluation and two SCF cycles to achieve convergence. Applications to atoms and small molecules are reported.
    Additional Material: 4 Tab.
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  • 89
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    International Journal of Quantum Chemistry 22 (1982), S. 1281-1305 
    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 first two members of the cyclic polyene homologous series are studied over a wide range of the coupling constant using the Hubbard and Pariser-Parr-Pople model Hamiltonians. The full and various limited configuration interaction (CI) correlation energies and wave functions are calculated exploiting the unitary group approach. The formalism for the cluster analysis of the exact wave function expressed through the unitary group formalism electronic Gelfand states is developed and applied to the full CI wave functions of the cyclic polyene models studied. It is shown that the connected tetraexcited clusters become essential in the fully correlated limit and that their contribution also significantly increases with electron number even for the coupling constant corresponding to the spectroscopic parametrization of the model Hamiltonians used.
    Additional Material: 11 Ill.
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  • 90
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    International Journal of Quantum Chemistry 21 (1982), S. 199-207 
    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: Several tunneling phenomena are surveyed. A unified, rigorous treatment of them can be based on a simple technique of integration by parts coupled with growth estimates of eigenfunctions, using, for example, WKB approximations. In particular, the analysis of Harrell and Simon of the resonance widths in the hydrogen Stark effect can be simplified.
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  • 91
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    International Journal of Quantum Chemistry 21 (1982), S. 195-197 
    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: It is proved that the Borel sum of the Rayleigh-Schrödinger perturbation expansion eigenvalue of the triple well anharmonic oscillators p2 + x2 - 2g2nx2n+2 + g4nx4n+2, g 〉 0, n = 2.3,… is a complex eigenvalue of a different problem. Its relation with the eigenvalues of the original Hamiltonian is discussed.
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  • 92
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    International Journal of Quantum Chemistry 21 (1982), S. 217-229 
    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
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  • 93
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    International Journal of Quantum Chemistry 21 (1982), S. 259-267 
    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 size consistency error formula, correcting for the erratic dependence on the number of particles in a doubly substituted (or otherwise restricted) configurational interaction (CI) treatment, is derived. The formula is expressed in terms of the particle pair eneriges ∊k and the normalization integrals Δk of the corrections to the unperturbed normalized wave function. The theory as well as the results for the 1A1 ground state of H2O and the 2B1 state of H2O+ show close agreement with the coupled electron pair approach (CEPA).
    Additional Material: 1 Tab.
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  • 94
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 95
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    International Journal of Quantum Chemistry 21 (1982), S. 411-418 
    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 symmetry groups of all trees are shown to be expressible as generalized wreath products by a tree pruning algorithm. The symmetry groups of certain cyclic graphs which can be expresssed as generalized compositions are also shown to be generalized wreath products. The symmetry groups of complete multipartite graphs can be obtained in a similar manner. Character tables of symmetry groups of certain chemical graphs are also obtained.
    Additional Material: 6 Ill.
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  • 96
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    International Journal of Quantum Chemistry 21 (1982), S. 813-822 
    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: CNDO/2 calculations have been performed on the clusters X4H9 and X4Y9 modeling the [111] diamond and silicon surfaces. The X is either carbon or silicon atom and the Y is a pseudoatom containing one sp3 hybrid orbital. It is shown that in the CNDO/2 approximation in the foregoing pseudoatom models, the charge distribution of the cluster is better than the hydrogen atom, because the electronegativity of the hydrogen differs significantly from the electronegativity of the sp2 orbital of the silicon atom. Using the CNDO/2 parametrization, the electronegativity of the hydrogen is very near to the electronegativity of the sp3 orbital of the carbon atom, thus the hydrogen can be used for the saturation of the carbon clusters.
    Additional Material: 1 Ill.
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  • 97
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    International Journal of Quantum Chemistry 21 (1982), S. 851-855 
    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 comparative analysis is carried out on the strengths of binding of a series of transition metal ions to a water molecule using CNDO type MO theory developed earlier. Comparative features of the energetics of metal-ligand bonds in aquo and amine complexes are also analyzed.
    Additional Material: 1 Tab.
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  • 98
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    International Journal of Quantum Chemistry 21 (1982), S. 591-610 
    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 bivariational scheme based on the general linear group of spin orbital space is presented, with the aim of obtaining approximations to the spectra of complex rotated Hamiltonians.
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  • 99
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    International Journal of Quantum Chemistry 21 (1982), S. 647-663 
    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: Using a canonical numbering of vertices for the graph corresponding to a particular rearrangement of tetragonal-pyramidal complexes, all 120 permutations defining the symmetry for the rearrangement are derived. An examination of the permutations points to the symmetric group S5, which has previously been found for isomerizations of trigonal-bipyramidal complexes and in the rearrangement of homotetrahedryl cations.
    Additional Material: 7 Ill.
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  • 100
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    International Journal of Quantum Chemistry 21 (1982) 
    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
    Type of Medium: Electronic Resource
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