No abstract

Static electric properties, from the dipole moment to the second-hyperpolarizability tensor γ, of the 3membered, isoelectronic ring molecules, fluorene (FL), carbazole (CR), and dibenzofuran (DBF), have been calculated at various levels of approximation. The electron correlation effects have been included at the coupled-cluster (CC) level, using CCSD and CC2 versions of the method. DFT calculations with the CAM-B3LYP functional have also been performed, and the results are compared to the CC values. The electric property-tailored Pol basis set and its more compact Z3Pol version have been employed in all static calculations. Differences between dipole polarizability values computed at the Pol and Z3Pol bases have been found to be almost negligible. Therefore, all components of the frequency-dependent dipole polarizability tensor α(−ω;ω) have been determined at the CAM-B3LYP/Z3Pol level. Divergence occurring at electronic resonances has been eliminated using the complex polarization propagator (CPP) formalism, explicitly introducing an imaginary iΓ parameter to account approximately for the finite lifetime of the excited state. The imaginary part of the dipole polarizability Im α(−ω;ω) has been calculated for a wide range of external radiation energies up to 10 eV, and its maxima have been compared to the calculated vertical electronic excitation energies.