Remarks on the use of approximate wavefunctions for the second-order perturbation energy.
Approximate ground state wave functions used in calculation of interaction energies by second- order perturbation theory
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Approximate ground state wave functions used in calculation of interaction energies by second- order perturbation theory
Study applies the nonequilibrium collision theory of reaction rates to the estimation of rate constants for simple reactions. The complications in the quantum mechanical description of chemical reactions and the care needed in approximating the exact wave function for the collision are shown.
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Recursion relations for Coulomb matrix elements, with psi and psi prime wave functions describing bound state
Partitioning technique to resolve total wave function of impure molecular crystal into two components
Ambiguities in perturbation equations solution for wave function proved to produce no corresponding ambiguities in energy
Remainder theorem of Rayleigh-Schroedinger perturbation theory for calculating wave functions to higher order
H molecule photoionization, using one center wave function with polarized orbital approximation to obtain oscillator strengths in 700 to 300 angstrom range
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