Abstract
A b initio complete active space (CAS) SCF and contracted CI calculations have been carried out for all valence and the lower Rydberg states of the benzene molecule. The CASSCF active space comprised 12 π-type molecular orbitals and the basis set included both polarization functions and diffuse functions in order to describe properly both valence and Rydberg type orbitals. Resulting excitation energies for the Rydberg states are in close agreement with experiment. CASSCF results for the valence states give errors ranging from 0.0 for the covalent states up to more than 1.0 eV for the most ionic states. Inclusion of σ–π correlation effects reduces the errors in the ionic states to less than 0.6 eV. The 1E1u state is computed to lie 7.4 eV above the ground state with a transition moment of 1.70 a.u., experimental values are 7.0 eV and 1.61 a.u., respectively.
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