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  • Theoretical, Physical and Computational Chemistry  (2)
  • Electron correlation and CI calculations  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Il nuovo cimento della Società Italiana di Fisica 17 (1995), S. 289-294 
    ISSN: 0392-6737
    Keywords: Electron correlation and CI calculations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Summary Valence Full Configuration Interaction (FCI) calculations are reported for the N2 molecule with a 4s3p triple-zeta basis set at different distances. The size of the FCI space is more than 225 000 000 symmetry-adapted Slater determinants. The computation requires about 1400 s of c.p.u. time per iteration on a CRAY C90, and is one of the largest FCI calculations ever converged. Our results, as is in general the case for FCI computations, can be used to test the performance of approximated methods used to study electronic correlation in molecules.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 63 (1997), S. 719-728 
    ISSN: 0020-7608
    Keywords: Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A direct full configuration interaction approach, previously used for studying individual low-lying eigenvalues, is combined with iterative Lanczos calculations, in order to obtain global properties of large Hermitean Hamiltonian matrices. To this effect systematic generation of random start vectors is used to compute statistical approximations to the density of states (DOS). Applications for cyclic polyenes in order to illustrate the viability of the scheme modeled by correlated, high-binding Pariser-Parr-Pople (PPP) Hamiltonians of increasing complexity are presented. The degree of correlation in the solutions is controlled by the parameter β. Convergence properties of the DOS for N = 10 and N = 14 are studied varying the extent of correlation. © 1997 John Wiley & Sons, Inc. Int J Quant Chem 63: 719-728, 1997
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 66 (1998), S. 397-407 
    ISSN: 0020-7608
    Keywords: cyclic polyenes ; exchange energy ; asymptotic behavior ; finite size correction ; Pariser-Parr-Pople ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The large N expansion of the restricted Hartree-Fock (RHF) exchange energy per atom E(N) of the Pariser-Parr-Pople (PPP) model of cyclic polyenes (annulenes) CNHN is derived in detail. We explicitly derive the coefficients E0 and E1 of the asymptotic expansion: E(N)=E0+E1 ln N/N2+O(N-2), N→∞, in the very simple case of half-filling and no bond alternation. The exchange energy per atom in the infinite chain can be written as Eex=(2/π2)∑∞j=1{[γ∞(2j-1)]/[(2j-1)2]}, where γ∞ is the two-electron repulsion integral in the infinite chain. On the other hand, the second coefficient E1 giving a finite-size correction is found to be 1/2b, where b is the bond length. This value of E1 differs slightly from that of a linear chain with periodic boundary conditions because the distance between sites depends upon the radius of the ring, i.e., upon N.   © 1998 John Wiley & Sons, Inc. Int J Quant Chem 66: 397-407, 1998
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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