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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 64 (1997), S. 481-494 
    ISSN: 0020-7608
    Keywords: Polyethylene ; energy bands ; dispersion relation ; Hamiltonian matrix eigenfunctions ; non-one-dimensionality ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The alternative way of solving secular problems for the Hamiltonian matrices of regular quasi-one-dimensional systems developed previously [V. Gineityte, Int. J. Quant. Chem. 60(3), 717 (1996)] has been applied to polyethylene. An implicit form of the dispersion relation has been obtained in terms of three local-structure-determined energy-dependent functions δ(ε), τ(ε), and η(ε), describing the effective interactions inside a separate CH2 group and those between first- and second-neighboring CH2 groups, respectively. The actual shapes of dispersion curves proved to be determined by relative mean values of the functions τ(ε) and η(ε) within the ε region under interest. The unusual minimum within the low-energy branch of dispersion curves situated at a low-symmetry point of the first Brillouin zone (k≈0.6π/a) has been established to appear owing to considerable values of effective interactions between the second-neighboring CH2 groups within the respective energy interval. Just the latter type of interactions has been concluded to be responsible also for non-one-dimensionality of the polyethylene chain. The Hamiltonian matrix eigenfunctions of this chain have been expressed as the Bloch sums of eigenvalue-dependent local-structure-determined basis orbitals.   © 1997 John Wiley & Sons, Inc. Int J Quant Chem 64: 481-494, 1997
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 68 (1998), S. 119-127 
    ISSN: 0020-7608
    Keywords: Brillouin theorem ; noncanonical MOs ; Rayleigh-Schrödinger perturbation theory ; saturated organic molecules ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The block diagonalization problem for a Fockian or a Huckel-type model Hamiltonian matrix (H) of molecule originating from the Brillouin theorem and determining the noncanonical molecular orbitals (NCMOs) has been studied. An alternative form of the problem, viz. the so-called eigenblock equation for the matrix H, has been suggested, which formally resembles the usual secular equation for certain two-dimensional matrix. The operator analog of the eigenblock equation also has been derived, and it acquired the form of the usual secular problem for an operator. However, the multidimensional eigenblocks of the matrix H, playing the role of eigenvalues in this new equation, do not commute with the respective multidimensional eigenfunctions. A noncommutative Rayleigh-Schrödinger perturbation theory (PT) has been developed for the solution of operator problems of the above-mentioned type. It has been shown that the PT used previously when obtaining the NCMOs of saturated organic molecules on the basis of the Brillouin theorem [V. Gineityte, J. Mol. Struct. (Theochem) 343, 183 (1995)] actually corresponds to the case of two eigenfunctions (eigenvalues) of the noncommutative Rayleigh-Schrödinger PT. On the whole, search for NCMOs of molecules is shown to be related to a nontrivial generalization of a two-level problem, where multidimensional (noncommutative) characteristics stand for the usual ones.   © 1998 John Wiley & Sons, Inc. Int J Quant Chem 68: 119-127, 1998
    Type of Medium: Electronic Resource
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