Abstract

Doppler-free two-photon absorption spectra of the A1Au←X1Ag(π*−n) transition of trans-glyoxal have been measured by means of two-photon absorption spectroscopy with counter-propagating light beams of identical photons within an external cavity. The relative energies of transition lines are measured with accuracy better than 0.0001 cm−1. Rotational lines are fully resolved, and 1809 lines of the A1Au(v7=1)←X1Ag(v=0) transition are assigned for J=0−75,K=0−17. Rotational constants of the A1Au(v7=1) and X1Ag(v=0) states are determined by a least-squares fitting of eigenvalues of the A-reduced rotational Hamiltonian to energies of the assigned lines. Energy shifts, intensity anomalies, and line splittings are observed for several lines. When an external magnetic field is applied, remarkable changes are observed for these lines. They are identified as originating from perturbations between the A1Au and a3Au states, which become appreciable when perturbing levels are close in energy. Splittings into three lines are observed for strongly perturbed levels of I=1, and these splittings are identified as the hyperfine splitting caused by mixing of the a3Au state.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call