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  • Articles: DFG German National Licenses  (5)
  • 1995-1999  (5)
  • Douglas-Kroll approximation  (3)
  • Cd  (2)
  • 1
    ISSN: 1432-2234
    Keywords: Key words: Polarized basis sets ; Relativistic effects ; Douglas-Kroll approximation ; Ionization potentials of group Ia and IIa metals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract. The technique previously developed for the generation of the so-called first-order polarized basis sets for accurate non-relativistic calculations of molecular electric properties is used to obtain similar basis sets suitable for calculations in the Douglas-Kroll no-pair approximation. The corresponding (relativistic) basis sets are constructed for atoms of groups Ia and IIa of the Periodic Table and tested in calculations of atomic and ionic polarizabilities. Also the first ionization potential of the group Ia and the first and second ionization potential of the group IIa metals have been evaluated to provide additional qualification of the generated basis sets. The present results are compared with earlier non-relativistic and quasirelativistic data and the role of the relativistic effect is discussed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0040-5744
    Keywords: Key words: Polarized basis sets ; Electric dipole polarizabilities of Zn ; Cd ; Hg ; and their positive ions ; Electron correlation effects on atomic properties ; Relativistic effects on atomic properties
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary. The first-order polarized basis sets are generated for Zn, Cd, and Hg and their performance is tested in high-level-correlated calculations of electric dipole polarizabilities of these atoms. The present results calculated at the level of the non-relativistic CCSD(T) approximation with 12 explicitly correlated electrons are: 40.4 a.u. for Zn, 56.3 a.u. for Cd, and 58.0 a.u. for Hg. Upon including the relativistic and electron correlation–relativistic corrections within the quasirelativistic scheme based on the mass–velocity and Darwin terms these values are reduced to 37.9 a.u., 47.6 and 31.8 a.u., respectively. The derived polarized basis sets have been also used for the evaluation of the dipole polarizability of singly and doubly positive ions of the group IIb elements and are recommended for calculations of interaction energies and interaction-induced electric properties in both neutral and charged systems.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0040-5744
    Keywords: Key words: Polarized basis sets ; Relativistic effects ; Douglas ; Kroll no-pair approximation ; Dipole polarizabilities of Zn ; Cd ; Hg ; Dipole moments of CuH ; AgH ; and AuH ; Polarizabilities of atomic ions: Cu+ ; Ag+ ; Zn2+ ; Cd2+ ; Hg2+
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary.  The technique developed earlier for the generation of the so-called first-order polarized basis sets for accurate non-relativistic calculations of molecular electric properties is used to obtain similar basis sets suitable for calculations in the Douglas–Kroll no-pair approximation. The corresponding (relativistic) basis sets are devised for atoms of the Groups Ib and IIb of the periodic table and tested in calculations of atomic polarizabilities and dipole moments of the coinage metal hydrides. Excellent performance of these basis sets has been found in the case of molecular calculations.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 68 (1998), S. 159-174 
    ISSN: 0020-7608
    Keywords: relativistic quantum chemistry ; relativistic connections to expectation valves ; two/one-component methods in relativity ; perturbation methods in relativity ; Douglas-Kroll approximation ; mass-velocity+Darwin approximation ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of the so-called picture change on expectation values of one-electron operators in approximate two(one)-component relativistic theories is discussed. This effect is expected to be particularly large for operators which assume large values in the vicinity of heavy nuclei. The numerical results illustrating the picture change effect on electric field gradients at nuclei have been obtained in the spin-free Pauli and Douglas-Kroll approximations. It has been found that the picture change effect lowers the electric field gradient at I in HI by about 1 a.u. Very large picture change effect (-8 a.u.) has been calculated for HAt. It is concluded that in accurate calculations of expectation values of operators involving high inverse powers of the electron-nucleus distance the picture change, which accompanies the transformation of the Dirac (Dirac-Coulomb) equation to approximate two(one)-component relativistic Hamiltonians, must be taken into account.   © 1998 John Wiley & Sons, Inc. Int J Quant Chem 68: 159-174, 1998
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0020-7608
    Keywords: relativistic Hamiltonians ; two-component methods in relativity ; perturbation methods in relativity ; Douglas-Kroll approximation ; regular approximations in relativity ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of nonsingular two-component relativistic Hamiltonians is derived from the Dirac Hamiltonian by first performing the free-particle Foldy-Wouthuysen transformation and then a block-diagonalizing transformation. The latter is defined in terms of operators which can be determined iteratively through arbitrary order in α, leading to transformed Hamiltonians with the two-component block accurate through α2k, k=1, 2, 3,… . These Hamiltonians give relativistic energies which differ from Dirac's energies only in terms higher than α2k. Their relation to other nonsingular methods of relativistic quantum chemistry (the Douglas-Kroll method, the regular Hamiltonian schemes) is discussed. By removing the spin-dependent operators, the derived Hamiltonians can be written in spin-free one-component form. The computational effort involved is essentially the same as in the case of the Douglas-Kroll scheme and amounts to relatively easy modification of the core Hamiltonian.   © 1997 John Wiley & Sons, Inc. Int J Quant Chem 65: 225-239, 1997
    Type of Medium: Electronic Resource
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