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  • Atomic, Molecular and Optical Physics  (2)
  • Organic Chemistry  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 5 (1992), S. 109-118 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A molecular mechanics study on some organophosphorus podands, with both rigid and flexible terminal groups, and on their complexes with Li+ and Na+ was carried out. Na+ causes smaller deformations of the ligands than Li+, but its complexes are less stable, as the interaction energy with the podands is weaker. The ligands with rigid terminal groups are, in general, more pre-organized for complex formation. The cation-ligand interaction energies, including also the changes in steric energies, are always higher in complexes of flexible molecules than in those containing rigid ligands. The lower entropy losses which accompany the formation of complexes of rigid molecules with alkali metal cations probably account for the observed higher stabilities of the complexes.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 6 (1993), S. 113-121 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A molecular mechanics study of cyclophosphazenic polypodands and of glymes, of their complexes with ion pairs (IPs) M+ I- (M+ = Li+, Na+, K+, Rb+) and IP aggregates (M+ I-)n was carried out to investigate the catalytic activity of these ligands in solid-liquid phase-transfer reaction. This activity is explained by their ability to bind IP aggregates effectively and to activate the anion by increasing the interionic distance in the single IP.
    Additional Material: 5 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 50 (1994), S. 401-410 
    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 problems connected with the simulation by the diffusion quantum Monte Carlo method of atomic and molecular systems in the two-dimensional (2D) space have been investigated on the 1 2S and 2 2S states of the hydrogen atom and on the 1 1S and 1 3S states of the helium atom, assuming r-1 Coulomb interactions between the particles. The potential surface of the 1Σg+ state of the 2D hydrogen molecule has been calculated in the range 0.1-1.5 bohr: A dissociation energy of 1.2703 Hartrees is found at the equilibrium distance of 0.3639 bohr. © 1994 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 57 (1996), S. 321-325 
    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 sampling of the exact solution of the Schrödinger equation by quantum Monte Carlo methods allows one to solve the problem of the optimization of linear and nonlinear parameters of a trial wave function by minimization of the distance to the exact wave function in Hilbert space even for those systems whose exact wave function is unknown. The overlap integrals between the basis functions and the exact wave function can be easily estimated within the quantum Monte Carlo formalism. Several observables of the helium atom ground state, computed both within the orbital approximation and by an explicitly correlated basis set, evidence the overall goodness of the wave function optimized according to this criterion. © 1996 John Wiley & Sons, Inc.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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