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  • 1985-1989  (138)
  • 1985  (138)
  • Atomic, Molecular and Optical Physics  (138)
  • 101
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 28 (1985), S. 691-701 
    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 multiconfigurational variation of moments (MCM) is presented to determine correlated orbital energies. Appropriate multiconfigurational one-particle operators are introduced starting for closed-shell systems from the restricted Hartree-Fock (RHF) scheme and for open-shell system from the unrestricted Hartree-Fock (UHF) scheme. The advantage of these operators is the linear form of the correlation energy in the configuration interaction (CI) coefficients. They obey HF analogous pseudoeigenvalue equations and are therefore a generalization of the HF operator. In principle, the scheme can be extended to a multiconfiguration self-consistent field (MCSCF) procedure for moments. In contrast to the SCF formalism they allow an orbital description of degeneracy and quasidegeneracy of the highest occupied (HOMO) and lowest unoccupied (LUMO) molecular orbital. With these operators, funnels of thermally forbidden Woodward-Hoffman reactions, as well as dissociations, can be described in a physically meaningful fashion by orbitalcorrelation diagrams.
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  • 102
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 28 (1985), S. 233-237 
    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 electron density at the pyridine nitrogen atom and the π-electron density of the pyridine ring were calculated by the CNDO/2-MO method assuming standard bond lengths and angles. The indices were found to correlate with the pKa values of pyridine derivatives and with the electronic substituent constants of the Hammett type. The correlations were best for four-substituted pyridines, making the routine CNDO/2-MO calculations useful for studies of quantitative relations between structure and biological activity of the compounds.
    Additional Material: 1 Tab.
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  • 103
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 28 (1985), S. 269-286 
    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
    Description / Table of Contents: We adapt the use of the Lie algebra su (n) we proposed in former papers to a system made up of two subsystems (respectively, nA and nB states). We show how reduced density operators, correlation problems, and overall and reduced evolution equations, may be made precise with this formalism.
    Notes: L'usage de l'algèbre de Lie su (n), proposé dans les articles précédents, est adapté a l'étude d'un système formé de deux sous-systèmes, respectivement à nA et nB états. On montre comment diverses notions (opérateurs-densités réduits, problèmes de corrélation, équations d'évolution globales et réduites) peuvent être précisées grâce au formalisme introduit.
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  • 104
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 28 (1985), S. 703-713 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A formalism was developed in the multiconfigurational variation of moments (MCM) framework, which yields physically meaningful orbital energies for occupied and virtual orbitals starting from self-consistent field (SCF) calculations. This is possible through a skillful distribution of the correlation energy on the orbital energies. The application of this method is demonstrated by SINDO1 calculations on the dissociation of H2 and the following symmetry-forbidden reactions: (1) torsion of ethylene; (2) ring opening of (a) cyclobutene, and (b) cyclopropyl cation; (3) cycloreversion of 1, 1-dicyano-2-methoxycyclobutane. The allowed reactions corresponding to 2a and 2b are investigated in the SCF scheme. The energy hypersurfaces are calculated for all reactions and the MO correlation diagrams are presented and discussed.
    Additional Material: 11 Ill.
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  • 105
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 28 (1985), S. 421-428 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have analyzed the dependence of the serotonin receptor binding affinity on the electronic and steric reactivity indexes for a group of 5-substituted tryptamines. The approaches employed are a new nonempirical Quantitative Structure - Activity relationship approach and multiple regression analyses. The results suggest that the variation of the receptor binding affinity in 5-substituted tryptamines is related to the variation of the net charge of two atoms and to the steric bulk of the N-substituent. A receptor model is proposed.
    Additional Material: 4 Ill.
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  • 106
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    International Journal of Quantum Chemistry 28 (1985), S. 757-771 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the 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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  • 107
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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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  • 108
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    International Journal of Quantum Chemistry 27 (1985), S. 135-144 
    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: PCILO computations have been carried out on the conformation of p-dimethylaminobenzylidene-p-nitroaniline [I(m)], p-nitrobenzylidene-p-dimethylaminoaniline [I(n)] and the corresponding stilbene [II(a)] and azobenzene [II(b)] derivatives. The aniline rings in Im and In are found to be twisted out of the plane containing the central atoms by 60° and 30°, respectively. The two phenyl rings in case of II(a) are twisted out of plane in opposite directions by 30° each. II(b) was found to be planar. The results have been compared with the earlier experimental findings and used as a possible explanation for the visible absorption spectra of the four molecules.
    Additional Material: 5 Ill.
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  • 109
    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 present numerical calculations of close-coupling equations to study vibrational predissociation of the T-shaped He…I2(B) van der Waals molecule. In the region of high vibrational excitation of the I2 subunit, the vibrational predissociation rates are related to the widths of the resulting resonances for the He-I2(B) collision. We apply a reasonable approximation to calculate the necessary background S matrix, i.e., the S matrix in absence of resonances. The rates of perpendicular vibrational predissociation, as a function of the initial I2 vibrational quantum number v1, show a maximum at v1 = 58 almost in agreement with the experimental data. However, an oscillatory and very interesting behavior of the rates in the region 60 ≤ v1 ≤ 65 is found.
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  • 110
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    International Journal of Quantum Chemistry 27 (1985), S. 231-232 
    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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  • 111
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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.
    Additional Material: 3 Ill.
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  • 112
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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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  • 113
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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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  • 114
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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.
    Additional Material: 4 Ill.
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  • 115
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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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  • 116
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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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  • 117
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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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  • 118
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    International Journal of Quantum Chemistry 27 (1985), S. 501-525 
    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 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.
    Additional Material: 9 Tab.
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  • 119
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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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  • 120
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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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  • 121
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    International Journal of Quantum Chemistry 27 (1985), S. 803-804 
    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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  • 122
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    International Journal of Quantum Chemistry 28 (1985), S. 27-37 
    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: 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.
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  • 123
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    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.
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  • 124
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    International Journal of Quantum Chemistry 28 (1985), S. 163-180 
    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: Extensive ab initio molecular-orbital calculations were carried out on trifluoromethylamine (TFM) to elucidate changes in geometry and electronic structure upon fluorination. The calculations show that the decomposition of CF3NH2 is slightly endoenergetic, and the heats of atomization of CF3NH2 and CH3NH2 show decreased stability of the species upon fluorination. Characteristic of CF3NH2 is a highly polar, strong, short CN bond. More limited calculations were carried out on CF3OH and CH3OH, and the electronic structure of CF3OH is found to be generally similar to that of CF3NH2. The reduced basicity of the fluorinated amine cannot be ascribed to the inductive effect; the enhanced acidity of the fluorinated alcohol reflects the weakening of the OH bond. No evidence leads to a confirmation of the existence of nitrogen-fluorine hyperconjugation in the fluorinated amine.
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  • 125
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    International Journal of Quantum Chemistry 28 (1985), S. 213-232 
    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 formalism developed in the first two papers of this series is applied to the investigation of a new weak-field model. This crystal-field model lies on the use of a symmetry-adapted weak-field basis and an effective Hamiltonian involving in a symmetrical way both spin- and orbit-dependent contributions. Some general properties of this Hamiltonian are studied and complete calculation of its matrix elements is conducted in a symmetry-adapted weak-field basis in the case of an arbitrary configuration nlN in any symmetry. The case of a configuration ndN in octahedral symmetry is fully explored. In this case, the proposed weak-field model is restricted to a 12-parameter model which accounts for isotropic and anisotropic Coulomb interactions, isotropic and anisotropic spin-orbit interactions, and crystal-field interactions. A comparison between this 12-parameter weak-field model and the 14-parameter strong-field model is established. Equivalence between the latter two models requires two constraint relations to be satisfied for some strong-field parameters. These two relations are examined with various viewpoints.
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  • 126
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    International Journal of Quantum Chemistry 28 (1985), S. 287-295 
    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 potential energy of a homonuclear X4 molecule is an invariant of the atom permutation group S4 acting on the internal coordinates of X4. It is shown by means of invariant theory that six algebraically independent invariants and five additional invariants are required to express the general invariant function for this group. Explicit expressions for these 11 invariants are given.
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  • 127
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    International Journal of Quantum Chemistry 28 (1985), S. 349-373 
    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: General formulas have been derived for molecular integrals arising in the use of the identity derived by Harriman for describing the Fermi-contact interaction in a molecule. Computational aspects are discussed and numerical examples are shown for several sets of the usual Cartesian Gaussian-type orbitals.
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  • 128
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    International Journal of Quantum Chemistry 28 (1985), S. 335-348 
    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 unitary group reformulation of electron propagator theory is used to derive the second-order and 2p - h Tamm-Dancoff self-energy approximations for open-shell applications. A highest weight representation of the reference state is chosen in order to facilitate matrix element evaluation, but two special cases precluded by this choice are also discussed. Detailed numerical calculations are described for the lithium atom, oxygen molecule, and the amidogen radical.
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  • 129
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    International Journal of Quantum Chemistry 28 (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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  • 130
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    International Journal of Quantum Chemistry 28 (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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  • 131
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    International Journal of Quantum Chemistry 28 (1985), S. 181-202 
    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 well known one-to-one correspondence between the eigenstates of the total spin for a system of spin-½ particles and irreducible representations of the symmetric group with up to two rows in the Young shape is the basis of interesting formal developments in quantum chemistry and in the theory of magnetism. As an explicit manifestation of this correspondence the class operators of the symmetric group are demonstrated to be expressible in terms of the total spin operator. This correspondence does not hold for higher elementary spins. The extension to arbitrary spin is investigated using Schrödinger's generalization of the Dirac identity, which expresses the transpositions in terms of two-particle spin operators. It is shown that additional operators, which for σ = ½ reduce to the total spin operator, are needed for a complete classification. Some aspects of the formalism are developed in detail for σ = 1. In this case a classification identical with that provided by the irreducible representations of the symmetric group is obtained in terms of the eigenstates of two commuting operators, one of which is the total spin operator.
    Additional Material: 2 Ill.
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  • 132
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    International Journal of Quantum Chemistry 28 (1985), S. 239-244 
    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: Based on the literature values, the pK1 and pK2 for pyrazine and its six methyl derivatives, the correlation with electron density on the nitrogen atoms N1 and N4 was found. The effect of methyl group was proved to be additive. The total electron density, π-electron density, and dipole moments for compounds under study were determined by the CNDO/2-MO method.
    Additional Material: 2 Ill.
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  • 133
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    International Journal of Quantum Chemistry 28 (1985), S. 297-309 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An ab initio investigation of the potential energy hypersurfaces of the Na+/H2 system is presented. The calculations have been performed on SCF level and with the inclusion of correlation effects by means of the CEPA-PNO, IEPA-PNO, and PNO-CI methods. The basis set consists of gaussian lobes (12s, 8p, d) on Na and (8s, p) on H. The distance of the Na nucleus to the midpoint of H2 was varied between 0.0 and 10 bohrs, whereas the region of H—H distances considered was 0.5 to 10 bohrs. The angular dependence of the hypersurface was investigated as well. The system Na+/H2 has an absolute energy minimum for C2v geometry at R equal approximately 5.0 bohrs and rHH = 1.40 bohrs.
    Additional Material: 4 Ill.
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  • 134
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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.
    Additional Material: 1 Tab.
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  • 135
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 28 (1985), S. 641-648 
    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 hybrid orbitals of tetrahedral oxy-ions containing some d character have been calculated by maximum overlap method. The d characters of hybrid orbitals increase in the order of SiO44-, PO43-, SO42-, ClO4-, and decrease in order of GeO44-, AsO43-, SeO42-, BrO4-. The bond strengths are also obtained for these ions. The hybrid Orbital of VO43-, CrO42-, and MnO4- are of the type d3s as the result of calculation.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 136
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    International Journal of Quantum Chemistry 28 (1985), S. 663-663 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 137
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 28 (1985), S. 665-686 
    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: This paper serves a twofold purpose. First, Löwdin's inner projection in both nonperturbative and perturbative forms is applied to the quartic anharmonic oscillator. Inner projection with perturbation theory yields rational approximations to Brillouin-Wigner-type perturbation expansions. These lower bounds are compared with [N - 1, N] Padé approximants to the Rayleigh-Schrödinger perturbation series for this problem. These Padés are also expressible as the even convergents, w2N, of a Stieltjes-type continued fraction. The latter representation has certain advantages with respect to its Padé counterpart. Inner projection without perturbation theory provides significantly better results than the perturbative version. The application of inner projection techniques to a perturbed hydrogen atom is not straightforward. The usual problems associated with the continuum spectrum of hydrogen are present. By means of a nonunitary “tilting” transformation associated with the Lie group SO(4, 2), these problems may be bypassed. In the SO(4, 2)-reformulated eigenvalue problem, a reinterpretation of the basic variables, as developed by Silverstone and Moats, yields a new Hamiltonian that permits direct use of the inner projection method. This method has been applied to the ground state of the hydrogen atom in a magnetic field, using both four- and eight-dimensional basis manifolds. This represents the first application of inner projection to this problem.
    Additional Material: 7 Ill.
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  • 138
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    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 28 (1985), S. 741-756 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A comparative study of quasirelativistic equations used in atomic structure calculations has been performed. A uniform derivation of all the equations is presented, and some of their specific features are discussed in detail. Electron density distributions, orbital energies, and expectation values of rn obtained with different methods are compared with the ones resulting from the Schrödinger and Dirac equations. The most accurate are found to be the equations of Wood and Boring and of Barthelat, Pelissier, and Durand. (They reproduce almost exactly the Dirac electron densities and expectation values.) The simplest, though least accurate, equation is proposed by us. It gives the relativistic energy corrections with about 6% accuracy and retains exactly the form of the nonrelativistic Schródinger equation. Consequently, its application in analytical SCF-CI calculations does not require any additional integral calculation.
    Additional Material: 4 Ill.
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