Use of the CNDO Method in Spectroscopy. I. Benzene, Pyridine, and the Diazines

Abstract

The CNDO method has been modified by substitution of semiempirical Coulomb integrals similar to those used in the Pariser‐Parr‐Pople method, and by the introduction of a new empirical parameter $\kappa$ to differentiate resonance integrals between $\sigma$ orbitals from those between $\pi$ orbitals. The CNDO method with this change in parameterization is extended to the calculation of electronic spectra and applied to the isoelectronic compounds benzene, pyridine, pyridazine, pyrimidine, and pyrazine. The results obtained were refined by a limited CI calculation and compared with the best available experimental data. It was found that the agreement was quite satisfactory for both $\mathrm{n\to \pi *}$ and $\mathrm{\pi \to \pi *}$ singlet‐singlet transitions. The relative energies of the pi and lone‐pair orbitals in pyridine and the diazines are compared and an explanation proposed for the observed orders. Also, the nature of the “lone pairs” in these compounds is discussed.