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  • Atomic, Molecular and Optical Physics
  • 1995-1999  (370)
  • 1985-1989  (138)
  • 1980-1984
  • 1975-1979  (99)
  • 1940-1944
  • 1995  (370)
  • 1985  (138)
  • 1975  (99)
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  • 1995-1999  (370)
  • 1985-1989  (138)
  • 1980-1984
  • 1975-1979  (99)
  • 1940-1944
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975), S. 1-8 
    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 this paper a calculation of the static quadrupole polarizabilities and the shielding factors of the atoms and ions of the 2p open shell systems is presented. A fully coupled Hartree-Fock method using the Roothaan formalism is adopted. Calculations have been done for the ground as well as for some valence excited states. An antishielding effect is observed for all the atoms and ions under study.
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  • 2
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975), S. 67-74 
    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 new integral transform function: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm exp }\left({{\rm - }\zeta {\rm r}} \right)\int_0^\infty {s(n)r^n dn} $$\end{document} where s(n) is a positive definite shape function, is proposed and investigated. A test on H2+ shows that it does not suffer from the inadequacies of earlier integral transform functions, of the form: \documentclass{article}\pagestyle{empty}\begin{document}$$ r^n \int_0^\infty {c(\zeta ){\rm exp}({{-}\xi r})d\zeta } $$\end{document} where c(ζ) is a positive definite shape function.
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  • 3
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975), S. 103-117 
    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: Weyl's eigenvalue theory for ordinary second-order differential equations is discussed for the case of a continuous spectrum. It is demonstrated that the spectral density function obtained from a suitably averaged Green's function, equal to the Weinstein function, can be directly related to the Weyl-Titchmarsh m-function. The explicit connections with scattering theory are derived and it is found that the Weyl and Jost solutions are proportional; the proportionality factor being the reciprocal value of the latter at the origin. The physical interpretation of the complex poles of the spectral density is discussed in relation to Gamow's exponentially growing functions. The advantage of using a formulation that allows for a “perturbation” of boundary conditions is pointed out.
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  • 4
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975), S. 149-156 
    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: Combined CI-HY method techniques have been employed in obtaining a 57-term CI-HY wave function with an energy of -14.66632 a.u. A method due to Brown has been adopted for obtaining this wave function and various shorter expansions. A 44-term expansion with an energy of -14.66606 a.u. is analyzed in terms of various pair effects, and qualitative arguments are presented for understanding these effects.
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  • 5
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975), S. 229-236 
    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: Mø-Plesset theory, in which electron correlation energy is calculated by perturbation techniques, is used in second order to calculate energies of the ground states of atoms up to neon. The unrestricted Hartree-Fock (UHF) Hamiltonian is used as the unperturbed system and the technique is then described as unrestricted Mø-Plesset to second order (UMP2). Use of large Gaussian basis sets suggests that the limiting UMP2 energies with a complete basis of s, p, and d functions account for 75-84% of the correlation energy. Preliminary estimates of the contributions of basis functions with higher angular quantum numbers indicate that full UMP2 limits give even more accurate total energies.
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  • 6
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975), S. 789-795 
    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 smooth interpolation method for the calculation of Fourier transforms of numerical atomic orbitals is presented and the method is used to calculate two-center overlap integrals. Examples applying various definitions of smoothness are given.
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  • 7
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    International Journal of Quantum Chemistry 9 (1975), S. 825-834 
    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 general variational principle for transition and density matrices is proposed. The principle is closely related to Rowe's variational treatment of the equations-of-motion method. It permits the simultaneous construction of coupled approximations for two eigenstates, and it is a straightforward extension of the usual variational method.
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  • 8
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975), S. 887-900 
    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 this paper we discuss an extension of the standard multiple scattered wave method for molecular electronic structure calculations to the case of arbitrarily shaped molecules. A general theory is presented where the difficulties arising from the matching problem across an arbitrary boundary are avoided. The secular equation to determine the energy spectrum is obtained and the wave functions are calculated in all regions.
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  • 9
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975) 
    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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  • 10
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975), S. 969-973 
    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: Reformulation, generalization, and application of Löwdin's symmetric orthonormalization, of orthogonalization of two sets of vectors, and of McWeeny's variational method of a density matrix, etc., by means of an operator for forming ket vectors on which are imposed some conditions, are presented.
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  • 11
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    International Journal of Quantum Chemistry 9 (1975), S. 1055-1067 
    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: Analytical formulas are derived for integrals of the orbit-orbit operator in the Breit-Pauli Hamiltonian. The present method differs from an earlier one in the introduction of a new auxiliary function Gn(a) which is an integral of Shavitt's Fm(t) function. A method for its evaluation is discussed and some numerical examples are given.
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  • 12
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    International Journal of Quantum Chemistry 9 (1975), S. 1109-1112 
    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 new method is presented for obtaining the spin eigenfunctions of 2n electron systems in the spin state S and MS = 0. Using a modified Young operator the function for the state S, MS ( = S) of the system is first projected out. The projected function is then symmetrized over the last n particles and the weight lowering operator Š-S is then applied to it, resulting in a projection of the state S, 0. To within a multiplicative factor, the resulting function is identical with the one resulting from the vector coupling methods.
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  • 13
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    International Journal of Quantum Chemistry 9 (1975), S. 379-381 
    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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  • 14
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    International Journal of Quantum Chemistry 9 (1975), S. 385-392 
    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 this communication we discuss a method of incorporating corrections to the coupled Hartree-Fock (CHF) formalism by introducing the so-called “rearrangement effect.” In this we take account of the relaxation of the core orbitals when excitations from a starting Hartree-Fock wave function occur. The magnitude of this correction numerically is found to be quite significant for the polarizabilities of two-electron atomic systems, results for which are reported.
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  • 15
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    International Journal of Quantum Chemistry 9 (1975), S. 431-443 
    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
    Notes: A perturbation approach based on resolvent technique and Padé approximants is proposed. The eigenvalue of interest is part of a solution of two nonlinear algebraic equations. The nonlinear equations are arrived at by considering two different expression of the expectation value of the resolvent of an outer projection of the Hamiltonian. The first expression is based on the spectral resolution of the resolvent, and the second one is obtained by a power series expansion analogous to that applied in the derivation of the energy expression in the Brillouin-Wigner perturbation theory. The truncated power series is extrapolated by Padé approximants of type II. The method is tested on a CI calculation of the energy of the lowest 1Σ state of the B2 molecule.
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  • 16
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    International Journal of Quantum Chemistry 9 (1975), S. 479-487 
    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: Complementary variational functionals are derived which impose upper and lower bounds on transition probabilities. These functionals are used to yield bounds in terms of sets of sum rules, and illustrative calculations are presented for hydrogen, helium and krypton atoms.
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  • 17
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    International Journal of Quantum Chemistry 9 (1975), S. 505-516 
    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: Dynamical screening in π-electron systems is studied by the equations of motion method. By using a partitioning technique on the equations of motion we can obtain simple expressions for the effect of dynamical screening directly on the transition energies and transition moments in π-electron systems. These results are used to study the effect of such screening in the N → V transition in ethylene. This procedure can be used to extend the equations-of-motion method to larger π-electron systems.
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  • 18
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    International Journal of Quantum Chemistry 9 (1975), S. 557-557 
    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
    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 report an attempt of ab initio computation for the ground-state wave-function of a few organic semiconductors (namely TCNQ salts and the PDC charge transfer complex) for which we show that electrical conduction appears to look strongly like that of a band-gap semiconductor.
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  • 20
    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: Some applications of an optimization technique due to Levenberg in theoretical submolecular biology are described. This technique has proved a very useful tool for the generation of three-dimensional structures of molecules having cyclic components or other constrained regions. The generated molecular structures provide the starting point for quantum chemical calculations of great value in solving problems of biological interest. The mechanism of transport of alkali metal cations by valinomycin is one such example and this paper describes briefly how various conformations of valinomycin were obtained using the optimization technique. A variant of the same method has been suggested as a new technique for the detection of topographical similarities between apparently dissimilar molecules which are substrates for the same enzyme or receptor site. The technique is illustrated with a comparison of a tricyclic antidepressant with norepinephrine both of which have been postulated to compete for a common receptor site in the “amine pump” of peripheral adrenergic nerve cell membranes. Another area in which the optimization technique has proved useful is in developing an optimum separable localized bond function method designed for rigorous calculations on large saturated molecules. This method is briefly described.
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  • 21
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    International Journal of Quantum Chemistry 9 (1975), S. 459-471 
    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 SCF-LCAO-MO calculations have been performed for TCNQ and its positive and negative ions in various electronic states. A basis set consisting of 412 primitive Gaussian type orbitals contracted to 180 was used in the investigation. The electron density distribution in TCNQ and the negative ions, and the redistribution upon ionization has been illustrated by plotting difference density contour maps. The quinone structure of the neutral TCNQ system undergoes a transformation to a benzenoid structure when electrons are added. Electronic transitions, ionization potentials and electron affinities have also been calculated.
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  • 22
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    International Journal of Quantum Chemistry 9 (1975), S. 517-526 
    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 extended Hartree-Fock equations of the spin-projected scheme are derived in a form suitable for the construction of a surely convergent method of solution using successive optimization of the individual orbitals. The derivation is based on a specific form of the generalized Brillouin theorem.
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  • 23
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    International Journal of Quantum Chemistry 9 (1975), S. 1113-1129 
    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: Valence-bond type wavefunctions based on contracted Gaussian atomic orbitals afford an adequate description of the potential of the ground 1Σg+ state of H2 for a wide range of internuclear separations. Semiempirical techniques for scaling the potential curve are evaluated. An efficient method for optimizing non-linear variables in the wavefunctions is explored.
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  • 24
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    International Journal of Quantum Chemistry 27 (1985), S. 97-101 
    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 provide an alternative to the biquadratic analytic scheme BIQ published earlier. This form, AMPLIN, is similar to the older linear analytic scheme, LIN. This scheme is much faster than BIQ.
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  • 25
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    International Journal of Quantum Chemistry 27 (1985), S. 105-105 
    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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  • 26
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    International Journal of Quantum Chemistry 27 (1985), S. 45-58 
    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 relations between isoscalar factors for corepresentations of antiunitary magnetic point groups are discussed in the case of associated corepresentations. The tables of the isoscalar factors for the single- and double-valued corepresentations of all tetragonal, orthorhombic, monoclinic, and triclinic Shubnikov point groups are given. Some peculiarities of the calculation method of the isoscalar factors for corepresentations are considered.
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  • 27
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    International Journal of Quantum Chemistry 27 (1985), S. 89-96 
    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 method of Dupuis and King for generating matrix elements of a totally symmetric one-electron operator in terms of symmetry-distinct integrals only is generalized to the case of nontotally symmetric operators. For operators constructed from two-electron integrals, explicit reduction of integral processing to permutationally inequivalent symmetry-distinct integrals only is described, while for one-electron operators further reductions are derived using double coset decompositions. Finally, some computational consequences of this approach are briefly discussed.
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  • 28
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    International Journal of Quantum Chemistry 27 (1985) 
    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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  • 29
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    International Journal of Quantum Chemistry 27 (1985), S. 145-157 
    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 orthogonalized direct diagonalization (ODD) method is used to predict the valence-shell ionization spectra for the series of hydrocarbons ethane (C2H6), ethylene (C2H4), and acetylene (C2H2) within an EOM/propagator formalism. Both (a) third-order and (b) higher-order (with h5 terms in the excitation operator manifold) calculations are presented in order to illustrate the effect of the extended operator manifold on the predicted valence-shell spectra. It is shown that the major effect of the h5 manifold is concentrated in its “occupied” part. Along with a general shifting of the main lines for outer valence ionizations to lower values (together with a slight reduction in pole strength), it is found that the effect of the h5 manifold in the inner valence region is dependent on the system being studied.
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  • 30
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    International Journal of Quantum Chemistry 27 (1985), S. 181-194 
    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 SCF MO calculations at the STO-3G level have been carried out on CH2OHOPO3-H and CH2OHOPO32-, which have been considered as model systems for the Cl-phosphate moiety of sugars. The results predict higher anomeric energy for the phosphate moiety at Cl atom of pyranosides. Also a trans arrangement of the exocyclic O - P bond is preferred rather than a gauche arrangement, thus exhibiting a reverse exo-anomeric effect. A complete potential energy map has been constructed for CH3OPO3-H, a model system for C6-phosphate moiety. It is seen that the bond angle optimization brings down the relative energies of various conformations. The effect of the phosphate group on the preferred conformation of phosphate containing polysaccharides is also discussed.
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  • 31
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    International Journal of Quantum Chemistry 27 (1985), S. 235-244 
    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: Internal rotation energy levels for phenol, fluoracetaldehyde, and difluoracetaldehyde are estimated with two methods: first, by means of the reduced inertia moment formula introduced by Pitzer; second, with use of an internal axis system and by taking into account the influence of the overall rotation through the inertia factor. Two methods have been used to estimate potential barriers (CNDO/2 and PCILO). Results are related to the asymmetry of the tops. Theoretical far IR spectra for the three molecules are calculated. In the case of phenol, good agreement is found with experimental data.
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  • 32
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    International Journal of Quantum Chemistry 27 (1985), S. 281-292 
    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 Hartree-Fock calculations are performed on hydrates of the F- and Cl- ions using 6-31G, 6-31G**, and 6-21G basis sets. Geometries and binding energies are obtained. An estimate of the correlation energy is provided by an MP2/6-31G (Møller-Plesset second-order perturbation) calculation. Comparisons are made between the Cl-(SO2) and the Cl-(H2O) complexes.
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  • 33
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    International Journal of Quantum Chemistry 27 (1985), S. 375-379 
    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 two-dimensional (2D) energy of the hydrogen molecule is carried out by the Heitler-London method. The 2D integrals (which are more localized compared to 3D ones) are performed in the light of the 3D Slater integrals. A discussion of such 2D systems is briefly outlined for doped semiconductors.
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  • 34
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    International Journal of Quantum Chemistry 27 (1985), S. 407-416 
    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 energy band of the molecular crystal NMP-TCNQ is calculated by means of the EHMO/LCAO-MO-CO method. In the calculation, both NMP and TCNQ are treated as quasi-one-dimensional columns, respectively. The results demonstrate that (i) the positions of the electronic energy bands of a molecular crystal are determined by that of the corresponding molecular orbitals of the respective isolated molecules; (ii) the widths of energy bands are determined by the interaction between the molecular orbitals of adjacent molecules in the crystal. These facts support the conclusion which we have given in the previous articles. The relationship between the structure of energy bands of the crystal NMP-TCNQ and its electrical conductivity at room temperature is discussed and compared with the crystal TTF-TCNQ. The differences of electrical conductivities of both crystals can be explained by the formula given by Fröhlich and Sewell.
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  • 35
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    International Journal of Quantum Chemistry 27 (1985), 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: The electronic structures of the π-π type complexes of pyridine with boron trihalides have been studied by means of IEHMO calculation. The results indicate that BX3(X = F, Cl, Br, I) tends to react with C5H5N in a planar configurations against the plane of C5H5N. The most stable configurations of complexes are at 60° of orientation angle ϕ for X = Cl, Br, I, but at 0° for X = F. A linear relationship between In Eb, the logarithm of rotation potential barriers, and the radii of halogen atoms r0 has been observed, and has been deduced from Morse potential function. In the complex, the donating properties of BX3 have an increase from X = F to I, and BF3 functions as an acceptor, but the others as donors. It has been shown that every energy level of the complex is corresponding to that of the donor or the acceptor, which we have discussed by the perturbation theory. The bonds between D and A appear essentially as π-π type but not pure.
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  • 36
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    International Journal of Quantum Chemistry 27 (1985), S. 547-557 
    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 redundancy-free internal valence compliance constants of open-chain water dimer and formic acid cyclic dimer have been determined by the combined use of the CNDO/Force method and the compliance constant formalism. The final compliant fields of these dimers have been refined with the help of experimental frequency data.
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  • 37
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    International Journal of Quantum Chemistry 27 (1985), S. 613-623 
    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 new method of evaluation of energy matrix elements has been derived for bonded functions of Boys and a spinless Hamiltonian. In configuration-driven CI algorithm the new approach is two to four times faster than the original Reeves' one, the relative speed depending on the case. In integral-driven CI the new approach is about 10 to 12 times faster than the equivalent approach based on the Reeves' scheme.
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  • 38
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    International Journal of Quantum Chemistry 27 (1985), S. 641-651 
    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 by means of the superposition of correlated configurations method (Hylleraas-CI), that is, the combination of configuration interaction with the Hylleraas-type correlation factors, needs the effective evaluation of some nontrivial integrals. This series of papers gives the formulas for all types of integrals needed for molecular calculations when Gaussian lobe functions are used as a basis set. The formulas for two-electron integrals are given in the present paper. The preliminary results for two-electron systems are presented.
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  • 39
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    International Journal of Quantum Chemistry 27 (1985), S. 699-707 
    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: An extended pairing scheme is presented which ensures the fulfillment of pairing conditions not only between the sets of occupied orbitals for spin α and for spin β, but also between their orthogonal complements, i.e., the sets of virtual orbitals for spin α and spin β, as well as between occupied orbitals for spin α and virtual orbitals for spin β and between virtual orbitals for spin α and occupied orbitals for spin β. It is shown that the extended pairing properties are suggested by some aspects of the construction of alternant molecular orbitals. The algorithm for singular value decomposition of rectangular matrices is proposed for use in practical implementations of the (extended) pairing scheme.
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  • 40
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    International Journal of Quantum Chemistry 27 (1985), S. 691-697 
    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 conventional partition functions of models with quadratically dependent energy spectra (e.g., translation in a box or free internal rotation), which are widely used in literature, exhibit an incorrect limit behavior in the region of low temperatures and/or small values of the characterizing molecular parameter. In particular, this leads to the absurd value  - ∞ for the contribution of these motions to the entropy term at these limit conditions. This incorrect behavior appears to be due to the replacement of rigorous summation by integration in conventional derivation of these partition functions. The derived improved practical formulas with the correct limit behavior indicate that it will be necessary to carry out quite substantial numerical corrections in the case of many reactivity characteristics reported in the literature. Particularly, the improved formulas should be applied with (small) molecular complexes at the typical temperatures of their observation, e.g., van der Waals molecules with free internal rotation. Simultaneously discussed is the possibility of application of the functional relation valid for a rigorous partition function of the considered type of energy spectrum. The reasoning in the case of the translational partition function indicates that, in principle, it can depend on the vessel shape. Possible consequences for thermodynamics of the ideal gas are analyzed.
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  • 41
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    International Journal of Quantum Chemistry 27 (1985), S. 709-730 
    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: N-representability conditions for a two-particle density operator implied by positive-semidefiniteness of the projection operator PN+1(φ1 Λ ΨN) are derived and discussed. The operator PN+1(φ1 Λ ΨN) projects onto an (N + 1)-particle antisymmetric function φ1 Λ ΨN, the Grassmann product of a one-particle factor φ1 and an N-particle factor ΨN. The polar subcone P2N(g, q) to the set of N-representable two-particle density operators P2N which corresponds to these conditions is found. It is shown that its extreme rays belong to two orbits for the action of the unitary group of transformations in one-particle Hilbert space. The facial structure of the convex set P2N exposed by elements of P2N(g, q) is analyzed. An example of the operator that changes the structure of its bottom eigenspace when the number of fermions N surpasses a certain value is noted. A new approach to the diagonal conditions for N-representability is found. It consists of the decomposition of the N-particle antisymmetric identity operator onto the mutually orthogonal projection operators.
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  • 42
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    International Journal of Quantum Chemistry 27 (1985), S. 781-786 
    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: Systematic ab initio LCAO MO calculations with basis sets of increasing size have been performed to analyze the changes in relative stabilization energies of the two cyclic (D3h and C3h symmetry) and the noncyclic HF trimers. The results form the basis for a discussion of cyclic H-transfer reactions.
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  • 43
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    International Journal of Quantum Chemistry 28 (1985), S. 1-16 
    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: The problem of ordering of chemical structures and subsequent comparison of their relative properties is initiated here by an approach which uses chemical points of view as well as graph theoretical considerations. Briefly, a collection of structurally related compounds (such as isomers, but even more broadly, compounds of similar chemical architecture even if involving different atoms) is examined pairwise and the degree of structural similarity is deduced from a comparison matching of their skeletons. Depending on the nature of the similarity found, some compounds qualify as related and are depicted as vertices of a graph with the corresponding connection. The derived “comparison graph” represents the framework for subsequent comparison of selected molecular properties. “Comparison graph” can also be viewed as depicting a hierarchy of dominance for the compounds and can be drawn with arcs (directed edges), or alternatively as a poset (partially ordered set). Usefulness of such viewing on a collection of structures is illustrated on hexane and heptane isomers and their properties. The results are discussed, particularly with respect to alternative ordering schemes. It was found that the present approach complements and does not duplicate other results, thus offering some novel structural insights.
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    International Journal of Quantum Chemistry 28 (1985), S. 311-314 
    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 maximum entropy procedure (MEP) of Jaynes has been extended to the case involving constraints in complementary spaces. It has been rigorously shown that the sum of information entropies in position and momentum spaces is invariant to uniform scaling of the electron coordinates. A new MEP procedure requires that this sum of entropies must be maximized subject to the known constraints in both spaces. A specific application of this maximization procedure for synthesizing atomic-electron densities in coordinate and momentum spaces has been outlined.
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    International Journal of Quantum Chemistry 28 (1985), S. 315-334 
    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 molecular orbital (CNDO/2) calculations on the key fragments of different dihydrofolate reductase inhibitors. Distance geometry analysis, physicochemical parameter dependent QSAR, and molecular shape analysis raised some questions regarding the basicity of the ring nitrogen (N1) in these inhibitors and the effect of the various substituents on the basicity. We show that the ring nitrogen N1 of methotrexate has a considerably higher tendency to be protonated compared to that of folic acid. However, not all 2,4-diamino inhibitors are equally basic. Even 2-amino-4-hydroxyquinazoline is sufficiently basic to be protonated, but not the 2,4-diamino-5-sulfonyl derivatives. The pyrimidinium ion seems to be highly solvated, since in spite of its high protonation energy it is strongly basic. Triazines were found to be the most basic of all the classes studied.
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    International Journal of Quantum Chemistry 28 (1985), S. 419-419 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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  • 47
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    International Journal of Quantum Chemistry 28 (1985), S. 399-409 
    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 studied the stability of guanine-cytosine and non-Watson-Crick pairs in the presence of H-bond interactions with various amino acid side chains, by using ab initio MO method. The external H-bond interactions stabilize or destabilize the base pairs, depending on the type of interacting residues and the site of the interaction. The pattern of the H-bond effect on the base-pair stability is quite different than in the case of adenine-uracil pair previously reported. From the present results, together with the previous results on adenine-uracil pair, we obtain a general rule for the effect of external H-bond interactions on the stability of base pairs. The site-specific effect of the H-bond interactions can be consistently explained by the cooperative interaction between external and base-pair H bonds. We discuss the application of the present results in the following biological processes: One is the protein-induced specific melting of double-stranded DNA, which is involved in transcription process. The present results suggest that H-bond interactions of protein residues at specific site of base pairs can weaken base-pair H bonding, which would assist the opening of double-stranded DNA. The other is the control of mutation in replication process. We suggest that proteins can discriminate non-Watson-Crick pairs against Watson-Crick pairs by H-bond interactions and can either induce or suppress mutation during DNA replication.
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    International Journal of Quantum Chemistry 28 (1985), S. 459-479 
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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 role of electron correlation effects on the bond-length alternation in linear metalliclike systems, as modeled by cyclic polyenes CNHN, N = 2n = 4v + 2, v = 1,2,…, is examined using the coupled cluster approach in the localized Wannier basis formalism. A recently developed approximate coupled pair approach which accounts for connected quadruply excited clusters is employed together with various truncation schemes for the localized doubly-excited cluster components. It is found that for the physical value of the coupling constant, the electron correlation has only a very slight effect on the potential energy curves, yielding almost the same values for both the magnitude of the bond-length alternation and for the stabilization energy relative to the symmetric equidistant structures as the restricted Hartree-Fock theory. This is in contrast to a strongly correlated region where the correlation effects stabilize the undistorted non-alternating structures. Different mechanisms of the bond-length alternation or Peierl's distortion as implied by a simple Hückel Hamiltonian and by the Pariser-Parr-Pople Hamiltonian models are also pointed out.
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    International Journal of Quantum Chemistry 28 (1985) 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    International Journal of Quantum Chemistry 28 (1985), S. 565-571 
    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/2 version of the average hole potential (AHP) model is analyzed. The model is applied to study the geometric features, molecular inversion barriers, singlet-triplet splittings, etc., of a few small carbonyl molecules (H2CO, HFCO, F2CO) in the 1,3nπ* states with partial as well as complete optimization of all geometric parameters in the excited states. The results are compared with those obtained by a simple hole-potential (HP) model.
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    International Journal of Quantum Chemistry 28 (1985), S. 603-607 
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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 generalization of a perturbation theory without wave function is developed which applies to a hydrogen atom perturbed by magnetic and electric fields. A double perturbation expansion for the Stark-Zeeman effect for parallel fields is considered and results for the states obeying |m| = l = n - 1 in the zero field limit are presented. Other problems that can be treated this way are discussed.
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    International Journal of Quantum Chemistry 28 (1985), S. 573-579 
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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 effects of four factors (different side chains, side-chain disorder, conformational change, and ions and water) on the energy band structures of proteins have been investigated with the aid of the CNDO/2 crystal orbital method. The results indicate that these factors are very important. The consequences of these effects on the semiconductive properties of proteins are discussed.
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    International Journal of Quantum Chemistry 28 (1985) 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    International Journal of Quantum Chemistry 28 (1985), S. 687-690 
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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 quality test for the SCF wave function based on separate examination of the one- and two-electron contributions to the total energy is proposed. The test is applied to 12 different STO basis sets for the ground state of the Ni atom and its predictions compared with those deduced for the minimization of the total energy. The new test allows for a reduction in the cancellation of errors detected in some applications of the standard SCF procedure. Some relations between the quality of the basis set and its size and structure are discussed.
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    International Journal of Quantum Chemistry 28 (1985), S. 723-729 
    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: Explicit expressions for integrals of the form 〈pu|∂/∂ν|s〉 occurring in expression of covalence reduction factors, introduced by Stevens and Tinkham, have been derived for various types of atomic functions. Numerical values of the integral for some common ligands are given. Misconceptions regarding the sign and the magnitude of this integral existing in the literature have been clarified.
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    International Journal of Quantum Chemistry 28 (1985), S. 757-771 
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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: In the framework of the additive SIBFA 2 procedure, the intermolecular interaction energy is computed as a sum of five terms: ΔE = EMTP + Erep + Epol + ECT + Edisp. In order to assess the accuracy of the procedure to compute cation-ligand interactions, the interaction of alkali (Na+, K+) and alkaline-earth (Mg2+, Ca2+) cations with two representative ligands H2O and HCOO- has been studied and the results compared with those of ab initio SCF extended basis set computations. The additive procedure reproduces very satisfactorily the results of ab initio computations as concerns the numerical values of the interaction energies and the equilibrium cation-ligand distances, as well as the evolution of the energy components. A detailed study of these components at different distances helps, in particular, to delineate the relative weights of the charge-transfer and polarization contributions within the second-order energy.
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    International Journal of Quantum Chemistry 9 (1975), S. 325-377 
    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 theoretical study is made of the states of nonrigid molecules, extending earlier work to apply Longuet-Higgins' symmetry group of feasible permutation/inversions in two previously untreated cases. The first involves nonrigid molecule processes between different stereoisomers, that is between molecular equilibrium configurations of different geometrical shapes. The second takes into account nonrigid molecule processes in linear molecules. The theory is applied to the specific case of nonrigid molecule effects in the butyl ion C4H9+ (case i), and the form of the nonrigid molecule energy levels and spectra are determined. The theory is also applied to determine the nonrigid molecule energy levels in linear H2F2 (case ii).
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    International Journal of Quantum Chemistry 9 (1975), S. 495-504 
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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: In this paper we include the rearrangement correction (discussed in the preceding paper) in a coupled Hartree-Fock (CHF) calculation of atomic hyperpolarizabilities and other related properties. We have studied the effect of these corrections on properties like electric dipole hyperpolarizabilities, uniform electric field quadrupole polarizabilities and shielding factors in two-electron ions and have noticed significant changes in the computed values over the CHF results.
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    International Journal of Quantum Chemistry 9 (1975), S. 555-555 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
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    International Journal of Quantum Chemistry 9 (1975), S. 545-554 
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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: We introduce here a new partitioning of the Hamiltonian in calculating pair-correlation energies using many-body perturbation theory, by which we are able to eliminate the off-diagonal particle-hole (p-h) ladders exactly to all orders in the perturbation expansion. In this formulation, the particle states turn out to be different for each distinct pair of hole states in the correlation energy calculation. We have also included the contributions of the diagonal particle-particle (p-p) and hole-hole ladders exactly to all orders. The effect of the off-diagonal p-p ladders has been estimated for each pair by computing the third-, foruth- and fifth-order energies. For highly symmetric systems the present partitioning yields in general symmetry-broken orbitals. Here one may use an average kind of partitioning for all the partners of the degenerate sets, which restores the symmetry and at the same time ensures cancellation of the p-h ladders exactly at the lowest order and approximately at the higher orders. Results are presented for a selection of 6π-electron conjugated systems. The correlation energy for each pair is in excellent agreement with that obtained from a partial CI calculation involving all double excitations from this pair. The advantages of implementing the present scheme in larger systems has been discussed.
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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 self-correlated field method is based on the insertion in the group product wave function of pair functions built upon a set of correlated “local” functions and of “nonlocal” functions. This work is an application to three-electron systems. The effects of the outer electron on the inner pair are studied. The total electronic energy and some intermediary results such as pair energies, Coulomb and exchange “correlated” integrals, are given. The results are always better than those given by conventional SCF computations and reach the same level of accuracy as those given by more laborious methods used in correlation studies.
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    International Journal of Quantum Chemistry 9 (1975), S. 669-681 
    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 modification of the concept of “seniority” for the classification of the permitted terms and the effective operators in complexes and molecules is presented. Tables of the states of complexes of impurity orbital nondegenerate ions (N = 3, 4) with spin S (\documentclass{article}\pagestyle{empty}\begin{document}$ S = \frac{1}{2} - \frac{7}{2} $\end{document}) and the corresponding tensorial operators are given.
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    International Journal of Quantum Chemistry 9 (1975), S. 711-719 
    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 few terms of the perturbation expansions for the function and the energy shift of a degenerate state of an arbitrary quantum mechanical system are obtained using the adiabatic formula. It is shown how the expansion for the secular operator may be obtained from the expansion for the function. The results are used to calculate energies of the ground and some excited states and multiplet splittings of some beryllium-like ions.
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    International Journal of Quantum Chemistry 9 (1975) 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    International Journal of Quantum Chemistry 9 (1975), S. 583-604 
    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: Recent advances in the statistical exchange approximation to the one-electron potential and in the use of general potentials in multiple scattering are studied numerically and combined in a cellular multiple scattering calculation of the electronic structure of molecules. The particular examples of these calculations are SF6, H2+, and H2, the results being compared with those of previous approximations and other techniques. It is first seen that the Xαβ approximation or a similar one based on the use of a universal parametrization of the statistical exchange (and some effects of correlation) part of the potential will provide the maximum of freedom in the partition of the real space of the molecules into cells. This avoids arbitrariness in the assumed value of the parameters to be used in every cell. The usefulness of the Xαβ approximation in a muffin-tin and in a cellular calculation is discussed. It is also found that the usual limitation to muffin-tin-like potentials, while simpler as a first approximation, can be removed without unduly increasing the computing effort. However, an accurate evaluation of the real self-consistent potential in each cell (or even in a muffin-tin) will increase the length of the program, the storage necessities and the computing time by a factor estimated to be between three and ten according to the geometry considered. It is concluded that the cellular multiple scattering method offers the best possibilities for a systematic use of multiple scattering techniques in molecular calculations.
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    International Journal of Quantum Chemistry 9 (1975), S. 605-625 
    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 structure and collective excitations of long molecules with conjugated bonds in the main chain (linear polyene, cyclic polyene, polyphenylacetylene (PPA)) are considered. The electronic structure of these polymers is investigated by the generalized Hartree-Fock method. The first triplet collective excitations are derived using the compact technique of the Green's functions. This approach is shown to be equivalent to the random phase approximation. The problem of the triplet collective excitations in long cyclic polyenes is solved analytically and good agreement with the exact results is found. The effects of the free ends in a linear polyene are considered. The approach developed for PPA and polyene may be applied to an investigation of any polymer molecule with equivalent unit cells.
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    International Journal of Quantum Chemistry 9 (1975), S. 657-668 
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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 concept of a “multi-centered plethysm” for multinuclear problems is defined and studied. Schemes of links of atoms in molecules or complexes and corresponding schemes of the group reductions are considered.
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    International Journal of Quantum Chemistry 9 (1975), S. 701-710 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: Three different forms of perturbation theories, variational perturbation, finite perturbation and second-order, are evaluated regarding their value for calculation of electronic polarizabilities of small and intermediate size molecules. It is concluded that with the practical constraint of a small basis set the variational perturbation method is the most promising alternative for calculation of polarizabilities. For several small molecules, our calculated polarizabilities indicate that both IEHT and ab initio wave functions give values in close agreement with each other. Variational perturbation calculations of polarizabilities with IEHT wave functions also include the DNA bases.
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    International Journal of Quantum Chemistry 9 (1975), S. 755-757 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    International Journal of Quantum Chemistry 9 (1975), S. 761-773 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: All the second-order density matrix spin components for the spin-projected Slater determinant are presented as expansions in direct products of powers of unprojected spin- and residual electron density matrices. Spin components of the second-order transition density matrices between spin-projected Slater determinants built of orthogonal orbitals are also obtained.
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    International Journal of Quantum Chemistry 9 (1975), S. 287-299 
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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: In order to test the effect of a removal of an “equivalence” restriction, some excited states of B, C+ and C arising from the configuration 1s22s2pn (n = 2, 3) are calculated by the use of a one-diffuse-electron model with the optimal spin coupling (DO), in which the freedom of the spin coupling is fully used. The configuration employed is 1s22s2pn-12p′ (n = 2, 3).The DO method gives a good agreement with the term energies especially for boron (4P → 2P) and carbon (5S° → 3S°). A diffuse 3p natural orbital with a large occupation number is found for boron 2P and carbon 3S° by DO. This result is confirmed by configuration interaction calculations.Using the same configuration as above, we also examine a one-diffuse-electron model with a fixed spin coupling for boron. This method almost reproduces the results of restricted Hartree-Fock and the effect of a removal of an “equivalence” restriction is not found.The importance of utilizing the freedom of the spin coupling in a one-diffuse-electron model is strongly indicated in this article.
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    International Journal of Quantum Chemistry 9 (1975), S. 855-870 
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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 comprehensive review of the attempts to rephrase molecular quantum mechanics in terms of the particle density operator and the current density or phase density operator is given. All pertinent investigations which have come to our attention suffer from severe mathematical inconsistencies and are not adequate to the few-body problem of quantum chemistry. The origin of the failure of these attempts is investigated and it is shown that a realization of a local quantum field theory of molecular matter in terms of observables would presuppose the solution of many highly nontrivial mathematical problems.
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    International Journal of Quantum Chemistry 9 (1975), S. 901-916 
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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: We present a method for calculating the one-particle Green's function for molecules. The scheme is essentially that proposed by Schneider and Taylor [1]. The Green's function is obtained through the Dyson equation. Closed expressions result by using the functional derivation technique to truncate an infinite set of coupled equations. A physical interpretation of the approximation is given and a connection with the equations-of-motion method is pointed out. In a numerical application the ionization potentials are obtained for the molecules N2, H2O, NH3 and CH4.
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    International Journal of Quantum Chemistry 9 (1975), S. 923-940 
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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
    Notes: Results of semiempirical calculations (CNDO/2-FK and MINDO/2 methods) for the σ-π complex problem on protonated benzene are given and compared with previous ones. The semiempirical methods were chosen according to the agreement of their results with new theoretical energy data (EHF + Ekorrel) concerning the classical-nonclassical problem of protonated ethylene. By these methods the corresponding part of the energy surface of the benzene/H+ system is simulated. The stationary points of this surface are found by a gradient method with complete optimization of the geometry. On the basis of this method we determined the energy profile of a reaction coordinate between the classical (σ-complex) and nonclassical (π-complex) cation. The so called strong π-complex is a saddle point between two σ-complex minima and can be interpreted as transition state of 1,2-proton shifts. Hypotheses for possible minimum energy paths of electrophilic attacks in the given region of the surface are discussed.
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    International Journal of Quantum Chemistry 9 (1975), S. 975-980 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: The convergence behavior of an iterative procedure proposed by Frost, Kellogg, and Curtis for solution of variance minimization equations is discussed. Use of particular sets of initial parameters in the iterative procedure is shown to yield rapid convergence.
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    International Journal of Quantum Chemistry 9 (1975), S. 1021-1031 
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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 computational technique within the Extended Hückel frame-work for the calculation of the hydrogen-molecule interaction energy is described. The procedure is ten times faster than the usual diagonalization procedure.The algorithm consists of transforming the generalized secular equation to give a bordered-diagonal matrix secular equation, which is solved by means of an efficient bisection technique.As an example, two problems are discussed: (i) glycine intra-molecular proton transfer process; (ii) interaction of the molecular fragments CH and OH.An atomic SCF Gaussian basis set was used instead of the usual Slater type basis set.
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    International Journal of Quantum Chemistry 9 (1975), S. 1069-1085 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: Using the variational method advanced by McCavert and Rudge, we obtain the independent particle model variational principle for loge localized discontinuous wave functions. The transformation of the variational expressions into matrix form when the loge localized discontinuous orbitals are expanded in finite basis sets is discussed. The simplifications brought about by this new method in the evaluation of molecular integrals are indicated.
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    International Journal of Quantum Chemistry 27 (1985), S. 233-234 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    International Journal of Quantum Chemistry 27 (1985), S. 245-257 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: Aiming at developing an approximate method to get good quality valence bond functions for any closed-shell delocalized system, we analyze their SCF functions in terms of weighted bonding schemes, and investigate the general rules relating the weights of ionic structures to those of covalent ones. The butadiene case is treated in details, and the results are generalized to all closed shell singlet conjugated molecules. It is demonstrated that, contrary to what an intuitive generalization of the two-electron-two-center model would predict, each bond is not described as a half-covalent, half-ionic entity, but that the ionic component is significantly preponderant. Some consequences on the behavior of conjugated systems under the influence of an electric field are discussed.
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    International Journal of Quantum Chemistry 27 (1985), S. 293-301 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: The introduction of local dielectric effects within the SCF theory of continuum solvent effects representation is examined at a semiempirical level. The formalism is developed in the frame of the reaction field theory within the effective charge approximation. The solvation free energies of Li+, Na+, F-, and Cl- ions in water were calculated in order to illustrate the reliability of the proposed model. The extension to molecules and molecular ions was performed including a desolvation corrective term related to the specific neighborhood of each atomic center. The results show a qualitative agreement with experimental data. A comment on the solvatonlike models for incorporating the solvent effect into the Hamiltonian is also given.
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    International Journal of Quantum Chemistry 27 (1985), S. 381-391 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: We establish a theorem which gives a necessary and sufficient condition for a set of matrix irreps of a finite group to admit real coupling (Clebsch-Gordan) coefficients. The proof is based on the method used by Feit to prove that a full set of coupling coefficients for a finite group determines the group up to isomorphism. A consequence of the theorem is that a finite group with real coupling coefficients is necessarily quasiambivalent. The theorem is used to demonstrate that real coupling coefficients do not exist for the point-group hierarchies T ⊃ D2 and I ⊃ T or for the double-group hierarchies I* ⊃ D3*, I* ⊃ D5*, and O* ⊃ D3*.
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    International Journal of Quantum Chemistry 27 (1985), S. 417-425 
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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 density operator of an n level quantum system is known to be a positive semidefinite, hermitian operator of trace one. In a previous article we have established, through su(n) algebras, a formalism where density operators are built from coherence vectors in a n2 - 1 dimension, real, Euclidean space. The last two conditions are then automatically satisfied. Being positive semidefinite means a restriction to the domain of coherence vectors. In this article we clarify this domain and obtain several equivalent tests to know if a given vector is part of it.
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    International Journal of Quantum Chemistry 27 (1985), S. 461-464 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: The rotational invariance of the Fock equations is investigated. It is demonstrated that the inclusion of d functions requires additional hybrid integrals which do not occur in the original version of INDDO. Calculations are performed with SINDO1 on binding energies, ionization potentials, and dipole moments to show the differences between the various levels of approximation.
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    International Journal of Quantum Chemistry 27 (1985), S. 501-525 
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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 new set of generators of the operator algebra over the electronic Fock space is introduced. It is shown that with this set of generators the “basis” Lie algebra can be associated and that the operator algebra of the Fock space is the homomorphic image of the corresponding universal enveloping algebra. The algebraic structure revealed is used for deriving the reduction formulas for the elements of the simplest spin tensor operators between the Gelfand states.
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    International Journal of Quantum Chemistry 27 (1985), S. 567-583 
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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: Here we present a detailed study of the theoretical approach to the tautomerization processes considering 2- and 4-oxo-pyrimidine and several of their derivatives. We look into molecular relaxation, suitability of semiempirical methods, and the effect of basis sets size in pseudopotential ab initio calculations. We found that no semiempirical method is suited for studying the relative stability of the tautomers, even ab initio calculations with minimal basis sets. On the other hand MNDO appears to be very useful for molecular relaxation and can be used, as well as Ab initio calculations, for reasonable estimates of relative tautomerization. We also considered the quality of prediction of other parameters, in particular the ionization potentials. We considered the correlation of experimental and theoretical values as a means to adjust the theoretical results to obtain more reliable predictions.
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    International Journal of Quantum Chemistry 27 (1985), S. 585-594 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: Recent Xα calculations of bond energies and other related properties of first-row diatomic molecules show very encouraging agreement with experiment. In the worst cases, however, the Xα dissociation energies overestimate the experimental values by almost 2 eV. Therefore, we have examined several refinements of the Xα theory and their effects on molecular bond lengths, bond energies, and vibrational frequencies. Among them, gradient corrections to the Xα exchange energy and also some variations of the local spin-density correlation energy approximation are considered. We find that a local exchange-correlation functional with gradient corrections gives dissociation energies in significantly better agreement with experiment than the Xα approximation.
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    International Journal of Quantum Chemistry 27 (1985), S. 637-637 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    International Journal of Quantum Chemistry 27 (1985), S. 625-635 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: A comparison of Roothaan-Hartree-Fock methods (both restricted and unrestricted) with density functional ones (LCAO-Xα and cellular MS-Xαβ) is made using as test case the He22 + molecular ion. It is shown the analogy that exists between RHF and symmetry-adapted LCAO-Xα potential energy curves, as well as between UHF and symmetry-unconstrained LCAO-Xα ones. The influence of symmetry adaptation on the overall behavior of the potential energy curve is also discussed. Finally, the difference in the behavior of the LCAO-Xα and cellular MS-Xαβ calculations is explained as an artifact of the space partitioning in the latter technique. It is concluded that LCAO-Xα method is superior to cellular MS-Xαβ because it requires less effort to reach the same results and that the general behavior is similar to UHF, although the former affords a better equilibrium bond distance and a worse energy barrier than the latter.
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    International Journal of Quantum Chemistry 27 (1985), S. 677-689 
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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 energies of the ground states of the mononuclear atomic systems, until now determined merely by approximate methods, turn out to exhibit some almost exact interdependencies. A simple statistical functional of the electronic structure (the “γ representation”) turns out to be decisive for the system energy. In this paper that interdependence is further traced for the N-electron systems in isoelectronic series (with constant N and varying Z). The resulting “combinatorial formula” reproduces the experimental data with the errors at least ten times smaller than those of the conventional Hartree-Fock approximation. The reason why there is such an exact formula for the ground-state energy remains to be clarified. The limiting behavior of our energy formula for large Z exhibits consistency with the Thomas-Fermi and the Z-1perturbation expansion models.
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    International Journal of Quantum Chemistry 27 (1985), S. 731-741 
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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 constant-denominator perturbation formalism is developed employing a basis of circulant orbitals and a projected Møller-Plesset partitioning of the Hamiltonian operator. A formal justification for the classical Unsöld approximation is thereby provided. A calculation of correlation energy in the beryllium atom is carried out, and the results are compared with results obtained by the full configuration interaction method and conventional Møller-Plesset perturbation theory.
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    International Journal of Quantum Chemistry 27 (1985), S. 787-801 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    International Journal of Quantum Chemistry 28 (1985), S. 17-26 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: An expression for electron transfer rate has been obtained through the solution of a time wave equation by the variational method by defining the wave function as a linear combination of functions corresponding to electron localization on the donor and on the acceptor. A dependence of electron transfer on temperature, on the electronic and vibrational characteristics of the system has been derived. An activation energy temperature-variation effect has been obtained. It has been proved that many-electron transfers are impossible.
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    International Journal of Quantum Chemistry 28 (1985), S. 61-84 
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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 propagator approximation scheme is presented in the context of an abstract*-algebra approach. The representation theory of such algebras is shown to play a crucial role in the definition of consistent approximations, i.e., approximate propagators based on model time evolutions and states. This procedure places superoperator methods of approximation on a sound Hilbert space footing. A generalization of the Fock vacuum property is introduced which leads to a simplification in the form of the model propagators. Finally a concrete example is considered that fulfills the conditions developed in this article showing that a consistent approximation to the electron propagator results in the Hartree-Fock-Boguliubov equations.
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    International Journal of Quantum Chemistry 28 (1985), S. 135-159 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: The widely cited definition of quantization in terms of square-integrable wave functions does not apply to continuum wave functions, to such phenomena as metastable states, or many-body resonances. A better philosophical foundation for quantum mechanics separates the probabilistic aspects based on square integrable Hilbert space functions from the dynamical aspects based upon the solutions of Shroedinger's (or Dirac's) equation. A Hilbert space may have a non-Hilbert space basis, which may be described by Stieltjes integrals and a spectrum measure. This viewpoint is expounded by reference to a very detailed analysis of a simple model, through which a precise definition of a Bohr-Feshbach resonance can be given. We propose a definition of a “metastable state,” showing that it is consistent with accepted usage, and that it overcomes a series of objections which have been catalogued by Simon. Its rate of decay is given by the Fourier-Stieltjes transform of the spectral density function; it is moreover the longest-lived initially localized state which can be formed from a small span of energy eigenfunctions near its mean energy.
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    International Journal of Quantum Chemistry 28 (1985), S. 203-211 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: N molecular orbitals are transformed to K(≦N) molecular orbitals, which are appropriate for an orbital optimization by two-by-two orthogonal rotations among themselves. This transformation is determined by using the second-order structure of the variational energy surface. The optimum K/2 rotation angles are exactly determined. This helps to ensure the reliability of convergence. K/2 two-by-two rotations are repeated among these K transformed orbitals. Then, two-electron molecular integrals are calculated by transformations among only 16 elements and by a permutation among K4/8 elements. Calculational time is considerably reduced compared with that of more usual transformations. Test calculations have been carried out on the ground state of CO. It shows that this procedure brings the calculation to the local region rapidly and reliably.
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    International Journal of Quantum Chemistry 28 (1985), S. 245-267 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    Topics: Chemistry and Pharmacology
    Notes: A method which is well suited for calculating numerically the energies of the bent vibrating and rotating polyatomic molecule is given. By an analytical method using ladder operators the work of calculating the matrix elements of the Watson Hamiltonian is reduced to mere bookkeeping. This results in fast computation and good control of the errors introduced. To demonstrate the practical usefulness of the method, three test calculations on H2O and SO2 are reported and compared with results from the literature. It is intended to distribute the computer program developed to interested workers in the field.
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    International Journal of Quantum Chemistry 28 (1985) 
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    International Journal of Quantum Chemistry 27 (1985), S. 803-804 
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    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
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    International Journal of Quantum Chemistry 28 (1985), S. 27-37 
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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: Ground-state energies of He, Be, and Ne isoelectronic series have been calculated. The Dirac-Hartree-Fock energy values have been corrected by adding Breit, vacuum polarization, self-energy, nuclear mass, and electron correlation corrections. The resulting energies are compared with the experimental values. As a result, an estimate of the correlation-relativistic cross-term energy is obtained. The effect, for large-Z atoms, proves to be quite substantial.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 100
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 28 (1985), S. 103-108 
    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: Wilson, Jankowski, and Paldus have recently applied nondegenerate many-body perturbation theory (MBPT) to simple models, in which the degree of quasidegeneracy could be varied continuously, and concluded that the nondegenerate theory was applicable even near degeneracy. The error in their results changes, however, considerably with geometry, leading to an incorrect potential surface. An extension of their calculations shows convergence even at exact degeneracy (square planar H4). It is shown here that the apparently good convergence is due to the suppression of the large (infinite at exact degeneracy) component of the perturbation energy in low order by the way the Hamiltonian is partitioned. This component will, however, resurface at higher orders, leading to slow convergence or even divergence. The low-order sum of the perturbation series is not very meaningful, depends strongly on details of the zero-order Hamiltonian, and yields, in general, incorrect potential surfaces. Multireference MBPT eliminates these problems.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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