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  • Computational Chemistry and Molecular Modeling  (11)
  • Wiley-Blackwell  (11)
  • American Association for the Advancement of Science (AAAS)
  • American Geophysical Union
  • PANGAEA
  • 1990-1994  (11)
  • 1993  (11)
Collection
Publisher
  • Wiley-Blackwell  (11)
  • American Association for the Advancement of Science (AAAS)
  • American Geophysical Union
  • PANGAEA
Years
  • 1990-1994  (11)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 47 (1993), S. 437-448 
    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 a symmetrical and adiabatic reaction path for hydrogen transfer from methane by methyl by an ab initio method using the 6-31G** basis set with the MP2 corrections for UHF/6-31G** optimized geometries. The theoretical barrier is fitted with the symmetric Eckart function. We, then, take thermal averages of the rate constant (k) considering the discrete nature of the C-H oscillators and the continuous character of the various low-frequency modes of the composite system. Finally, we present a linear relation between log k and temperature. It is shown that this relation gives a good description of the kinetic results of both thermal and photochemical H-transfer reactions in the region of low temperatures. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 45 (1993), S. 363-383 
    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 derived the necessary conditions to which the vector coupling coefficients (VCC) amn and bmn, describing atomic L, S-multiplets of pMdN and dNs1 configurations (1 ≤ N ≤ 9, 1 ≤ M ≤ 5), should satisfy. It is shown that for two-open-shell systems under consideration the unknown VCC should satisfy not only usual restrictions resulting from the spheric symmetry, but also some additional equation introduced in the present paper in the form of a postulate. VCC obtained were used for the ab initio calculations (by the general SCF coupling operator method) of several transitionmetal atoms and ions with electronic configurations 3d14p1, 3p43d3, and 3p53d3. To check the presented theory, we carried out a detailed comparison between these results and analogous data, obtained by the atomic Roothaan-Hartree-Fock method [2]. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 45 (1993), S. 71-85 
    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 variational principle for the transition matrix is considered. Conception of the MC SCF (in particular, CASSCF) approach for the transition matrix is proposed as a solution of the variational problem on the optimal evolution of a packet of two stationary states with some additional conditions. An ordinary MC SCF method for a single state is a special case of the proposed approach. Some aspects of the solving of the equations for the optimal transition matrix are treated. The method can be used in atomic and molecular calculations of transition energies, oscillator strengths, and other properties. © 1993 John Wiley & Sons, Inc.
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  • 4
    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 carbon dioxide (CO2) to methylamine (CH3NH2) addition reaction is investigated using an ab initio MO method with the aim of obtaining an insight into the relation between transition-state structure and reactivity. The complete potential energy hypersurface was explored and the stationary points representing reactants, transition state, and product were localized. To establish the relevance of different basis sets, calculations were carried out at different levels of theory: STO-3G, 3-21G, 4-21G, 4-31G, 6-31G, 6-311G, 6-31G*, and MP2/6-31G*//HF/6-31G*. A reaction analysis done by correlation of bond-order indices using the More O'Ferrall-Jencks diagram reveals the reaction mechanism as an asynchronous process. The transition state can be described as a four-membered ring. The lone nitrogen electron pair of the amine appears as the driving force of the reaction, where a positive hydrogen rather than a radical is more likely to be transferred. © 1993 John Wiley & Sons, Inc.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 46 (1993), S. 55-71 
    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 SCF analysis has been carried for ensembles that simulate the CuO2 conduction layer in the tetragonal layer crystal T′ - Nd2CuO4 (Fig. 1). In this work, the CuO2 layer is described by a planar macromolecule, (CuO2)n, subject to the crystal field produced by the point charges in the ionic layers of D4h symmetry The computations were carried out using the KGNMOL, HONDO, and KGNGRAF codes in MOTECC -91. The computations were carried out with different oxygen and copper basis sets and energy convergence to less than 10-8 Hartrees. The purpose of the SCF computation was to estimate the cohesive energy of the ensembles, the electron density for the individual molecular orbitals, and the excess correlation energy, to ascertain the nature of the Cu—O bond in the conduction layer. The results indicate the following: (1) The cohesive energy of the ensembles (measured by the SCF energy plus the correlation energy, above the atomic values): ΔUc ≡ ΔESCF + ΔEC = -4.35 to -4.17 Hartrees per CuO bond as n increases from 4 to 9. Further insight was obtained by considering the electrostatic energy contributions to ΔUc; Eelectrostatic (ensemble) → EModeling (infinite lattice) were evaluated by replacing the oxygen and copper atoms by point charges determined by a Mullion population analysis. The larger oxygen basis set (13, 8/5,3) gave consistent results for the different ensembles of ΔEcovalent ≡ ΔUc - Eelectrostatic = -1.1 Hartrees per CuO bond. (ii) The electron density indicates that covalent bonds are formed and that the oxygen atoms play an important role in the structure stability. The covalent bonds formed indicate that nominal ionic valences do not apply. Mulliken population analyses gave valences of the order of one at the copper and oxygen atoms. The CuO bond orders are 0.47 between neighboring atoms and 0.048 for those separated by two atoms. (iv) The covalent nature of the CuO bonds in (CuO2)n was compared to that for the H2 molecule using as a measure the electron density and the excess correlation energy. The excess correlation energy per CuO bond above the atomic values is one order of magnitude lower that that for the H2 molecule and that for the C=C bond in alternant hydrocarbons. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 46 (1993), S. 295-317 
    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 brute-force numerical investigation has been carried out on the hopping of excitons in a three-dimensional molecular aggregate. Possibilities of vibronic decay, rapid chemical reactions of saturated species, radiative decay of overpopulated molecules, and cooperative chemical reactions involving saturated exciton populations on traps of two different types have been considered. Investigation have been performed with two types of initial distribution of excitons - facial and random - and for 10,000 or, sometimes, for 20,000 time steps each of duration 1ps. Several interesting observations have been made from this computer experiment: (1) The total number of occurrences of fast reactions depends upon the initial distribution of excitons. (2) It decreases if other exciton depleting processes are at work. (3) It also depends on the pattern of placement of traps. (4) The location of impurities also affects the rate of occurrence of these reactions. Thus, more reactions occur when the excitons are initially concentrated on one face and traps are suitably located on the path of flow of these excitons. A random initial distribution tends to equilibrate the excitons quickly over all the lattice points, thus giving rise to fewer reactions. (5) The number of reactions need not necessarily increase with the number of reaction centers; in fact, it decreases as more centers are added when the supply of excitons is severely limited. (6) A Complicated dynamics results when different types of additional processes, viz., enhanced fluorescence, radiative emissions, and cooperative chemical reactions are simultaneously allowed. The cooperative process has been clearly found to dominate. A first-order rate constant of about 108 s-1 has been calculated for the occurrence of the cooperative process. This rate is affected when other nonconserving processes are switched on. Observations (1), (4), and (5) are the most important conclusions of our work. They lie outside the scope of traditional models such as the random walk model, the diffusion model, and the lattice model for the migration of excitons in a molecular aggregate. © 1993 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 48 (1993), S. 407-418 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the Dyson equation, the self-energy describes all relaxation and correlation corrections to Koopmans's theorem. Energy-independent contributions to the self-energy depend on the one-electron reduced density matrix of the reference state. Three formalisms for calculating these terms are considered: perturbation theory, coupled-cluster theory, and contour integral theory. In one method, combinations of coupled-cluster singles and doubles amplitudes are substituted for first-order double excitation coefficients and for second-order single excitation coefficients. Another approach generates a description of reference state correlation through the evaluation of approximate contour integral expressions. Calculations on electron binding energies of closed-shell molecules and anions reveal that the coupled-cluster results for the energy-independent self-energy terms are closer to the perturbative results than to the contour integral values. © 1993 John Wiley & Sons, Inc.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 46 (1993), S. 577-582 
    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 Hubbard model of the polyallyl chain with a strong repulsive potential and one hole in the half-filled band is reduced to the effective spin Hamiltonian. In the case of infinite repulsion, the exact spectrum of the model with cyclic boundary conditions is obtained.© 1993 John Wiley & Sons, Inc.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 48 (1993), S. 687-698 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple model Hamiltonian is used to calculate the limit of zero-voltage resistance in a one-dimensional chain of one-state sites. The end atoms in the chain are considered to be chemisorbed to the surface of the metal electrodes and their interaction with the continuum of metal states (jellium model) is treated as in the Anderson-Newns chemisorption theory [1,2].For this model, an exact solution can be obtained for the zero-voltage resistance within the formalism developed by Doyen and co-workers [3] for the calculation of the current in Scanning Tunneling Microscopy (STM). Applications of the results described in this article to the problem of molecular imaging in STM are presented elsewhere [4,5]. © 1993 John Wiley & Sons, Inc.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 48 (1993), S. 699-711 
    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 calculated the first-, second-, and third-order contribution to the refractive index of a dilute aqueous solution of three-level molecules irradiated by an intense one-frequency external field. Each solute molecule is described by two coupled harmonic curves of electronic energies with the same force constant and with minima displaced in energy and nuclear coordinate. We assume that the intramolecular coupling mixes only the states corresponding to two near degenerate of the three levels considered. Important linear and nonlinear contributions of the solute molecules to the refractive index have been found, mostly in the so-called weak and intermediate coupling regions. © 1993 John Wiley & Sons, Inc.
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