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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Theoretical chemistry accounts 73 (1988), S. 81-103 
    ISSN: 1432-2234
    Schlagwort(e): Many-electron correlation problem ; Spin-adaption ; Unitary group approach ; Coupled-pair approach ; Configuration interaction
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract An essential role of Clifford algebras for quantum-chemical finite-dimensional orbital models of many-electron systems is pointed out. The relationship between Clifford algebra matric units, the generators of the unitary group approach (UGA) and the higher order replacement or excitation operators, as well as between their first and second quantized realizations, is elucidated. The usefulness of higher order replacement operators in the spin-adaptation of various many-body theories is briefly outlined and illustrated on the orthogonally spin-adapted coupled-pair approach. A natural connection with the Clifford algebra UGA is explored and new possibilities for its exploitation in large scale configuration interaction calculations are suggested.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 56 (1995), S. 129-155 
    ISSN: 0020-7608
    Schlagwort(e): Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: We show that the irreducible tensor operators of the unitary group provide a natural operator basis for the exponential Ansatz which preserves the spin symmetry of the reference state, requires a minimal number of independent cluster amplitudes for each substitution order, and guarantees the invariance of the correlation energy under unitary transformations of core, open-shell, and virtual orbitals. When acting on the closed-shell reference state with nc doubly occupied and nv unoccupied (virtual) orbitals, the irreducible tensor operators of the group U(nc) ⊗ U(nV) generate all Gelfand-Tsetlin (GT) states corresponding to appropriate irreducible representation of U(nc + nv). The tensor operators generating the M-tuply excited states are easily constructed by symmetrizing products of M unitary group generators with the Wigner operators of the symmetric group SM. This provides an alternative to the Nagel-Moshinsky construction of the GT basis. Since the corresponding cluster amplitudes, which are also U(nc) ⊗ U(ns) tensors, can be shown to be connected, the irreducible tensor operators of U(nc) ⊗ U(nv) represent a convenient basis for a spin-adapted full coupled cluster calculation for closed-shell systems. For a high-spin reference determinant with n, singly occupied open-shell orbitals, the corresponding representation of U(n), n=nc + nv + ns is not simply reducible under the group U(nc) ⊗ U(ns) ⊗ U(nv). The multiplicity problem is resolved using the group chain U(n) ⊃ U(nc + nv) ⊗ U(ns) ⊃ U(nc) ⊗U(ns)⊗ U(nv) ⊗ U(nv). The labeling of the resulting configuration-state functions (which, in general, are not GT states when nc 〉 1) by the irreducible representations of the intermediate group U(nc + nv) ⊗U(ns) turns out to be equivalent to the classification based on the order of interaction with the reference state. The irreducible tensor operators defined by the above chain and corresponding to single, double, and triple substitutions from the first-, second-, and third-order interacting spaces are explicitly constructed from the U(n) generators. The connectedness of the corresponding cluster amplitudes and, consequently, the size extensivity of the resulting spin-adapted open-shell coupled cluster theory are proved using group theoretical arguments. The perturbation expansion of the resulting coupled cluster equations leads to an explicitly connected form of the spin-restricted open-shell many-body perturbation theory. Approximation schemes leading to manageable computational procedures are proposed and their relation to perturbation theory is discussed. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 7 Tab.
    Materialart: Digitale Medien
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  • 3
    ISSN: 0020-7608
    Schlagwort(e): Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The orthogonally spin-adapted (OSA) coupled-pair (CCD) methods with an approximate account of triply and quadruply excited clusters are considered. We focus on the CCD + ST(CCD) perturbative estimate of the singly and triply excited clusters due to Raghavachari [J. Chem. Phys. 82, 4607 (1985)] and its ACPQ + ST(ACPQ) analog proposed by Paldus and Piecuch [Int. J. Quantum Chem. 42, 135 (1992)]. The latter approach combines the perturbative treatment of singles and triples with an approximate CCD theory corrected for connected quadruply excited clusters (ACPQ). We also consider the OSA version of the CCSD + T(CCSD) method (coupled-cluster [CC] approach with singly and doubly excited clusters and noniterative perturbative account of triply excited clusters) introduced by Urban et al. {J. Chem. Phys. 83, 4041 (1985)}. The explicit OSA expressions for the previously neglected {P. Piecuch and J. Paldus, Theor. Chim. Acta 78, 65 (1990)} S(CCD) and S(ACPQ) terms are derived using diagrammatic methods of many-body perturbation theory and graphical methods of spin algebras. The CCD + ST(CCD), CCSD + T(CCSD), and ACPQ + ST(ACPQ) formalisms have been implemented and the general purpose ab initio programs have been written using a newly developed procedure for improving the convergence of the reduced linear equation method {P. Piecuch and L. Adamowicz, J. Chem. Phys. 100, 5857 (1994)}. Results of the pilot calculations for few nondegenerate and quasi-degenerate systems are presented and compared with the full configuration interaction data. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 5 Tab.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 60 (1996), S. 513-527 
    ISSN: 0020-7608
    Schlagwort(e): Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The problem of bond length alternation in linear extended φ-electron systems with conjugated double bonds is examined using the valence bond theory applied to a simple model of cyclic polyenes CNHN with N = 4v and N = 4v + 2 sites as described by the Pariser-Parr-Pople Hamiltonian. Overlap enhanced atomic orbitals are employed in order to achieve the optimal treatment with only two Kekulé structures. The predicted bond length alternation and its magnitude are in good agreement with earlier molecular orbital based calculations and with experiment. Special attention is given to the discussion of the origin of bond length alternation in long polyenic chains and to the role of the resonance energy leading to stabilization of undistorted, symmetric structures for small aromatic (N = 4v + 2) cycles. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 40 (1991), S. 9-34 
    ISSN: 0020-7608
    Schlagwort(e): Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: It is shown that the exact pair-cluster coefficients corresponding to the fully correlated limit of cyclic polyene model satisfy the equations of the approximate coupled-pair theory with quadruples (ACPQ) approach, but do not represent any solution of the standard coupled-cluster method with doubles (CCD) equations. Implications of this result for the performance of various coupled-cluster (CC) approaches, when applied to cyclic polyene model, are discussed.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 41 (1992), S. 117-146 
    ISSN: 0020-7608
    Schlagwort(e): Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A detailed algorithm is described that enables an implementation of a general valence bond (VB) method using the Clifford algebra unitary group approach (CAUGA). In particular, a convenient scheme for the generation and labeling of classical Rumer-Weyl basis (up to a phase) is formulated, and simple rules are given for the evaluation of matrix elements of unitary group generators, and thus of any spin-independent operator, in this basis. The case of both orthogonal and nonrothogonal atomic orbital bases is considered, so that the proposed algorithm can also be exploited in molecular orbital configuration interaction calculations, if desired, enabling a greater flexibility for N-electron basis-set truncation than is possible with the standard Gel'fand-Tsetlin basis. Finally, an exploitation of this formalism for the VB method, based on semiempirical Pariser-Parr-Pople (PPP)-type Hamiltonian and nonorthogonal overlap-enhanced atomic orbital basis, and its computer implementation, enabling us to carry out arbitrarily truncated or full VB calculations, is described in detail.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 42 (1992), S. 165-191 
    ISSN: 0020-7608
    Schlagwort(e): Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Perturbation expansion for the ground-state energy in the strongly correlated limit of cyclic polyenes, as described by the Pariser-Parr-Pople (PPP) and Hubbard Hamiltonians, is examined. Focus is placed on the first- and second-order contributions in terms of the resonance integral, and the performance of the approximate coupled pair theory corrected for the connected quadruple excitations (ACPQ), as well as ACPTQ and ACPQ + T(ACPQ) methods, which are two different versions of ACPQ approximately accounting for the triexcited clusters, is studied. The second-order contribution obtained with the ACPQ, ACPTQ, and ACPQ + T(ACPQ) approaches is then compared with the exact result for the fully correlated limit as provided by the diagonalization of the nearest-neighbor Heisenberg Hamiltonian. It is shown that all three coupled pair theories yield vanishing first-order contribution, in agreement with the exact result. The best result for the second-order contribution for the cyclic polyenes considered in this article is provided by the ACPQ + T(ACPQ) method. In this respect, all three coupled pair theories seem to deteriorate as the polyene size approaches infinity, in spite of yielding excellent energies. Comparison is also made with the results of alternant molecular orbital method.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 21 (1982), S. 147-151 
    ISSN: 0020-7608
    Schlagwort(e): Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: We estimate radii of convergence of the Rayleigh-Schrödinger perturbation expansions for various energy levels of the π-electron model of the benzene molecule, described by the Hubbard Hamiltonian in both weakly and strongly correlated limits. They are determined using a “generalized” Cauchy criterion applied to the numerically determined coefficients of the pertinent expansions.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 34 (1988), S. 407-415 
    ISSN: 0020-7608
    Schlagwort(e): Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The ground state energies of finite Hubbard molecules are calculated by numerically solving the Lieb-Wu equations for a complex Hubbard repulsion parameter U. From the positions of the singular points located in the complex plane, the radii of convergence of the perturbation expansions for the ground state energies are determined.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 36 (1989), S. 127-140 
    ISSN: 0020-7608
    Schlagwort(e): Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A explicit expression for the unitary group Clebsch-Gordan coefficients, which couple two fully antisymmetric single-column states into the two-column Gel'fand-Tsetlin states, is given in terms of isoscalar factors for the canonical subgroup chain U(n) ⊃ U(n - 1) ⊃ … ⊃ U(1). The isoscalar factors are expressed through the step numbers labeling canonical basis states and enable a straightforward construction of Gel'fand-Tsetlin states in the Clifford algebra unitary group approach, without the use of the tables for the symmetric group outer-product reduction coefficients.
    Materialart: Digitale Medien
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