Rydberg-valence interactions of CO, and spectroscopic evidence characterizing the C′1Σ+ valence state

Rotationally cold absorption and two-photon ionization spectra of CO in the 90-100 nm region have been recorded at a resolution of 0.3-1.0 cm-1. The analyses of up to four isotopomers seek to clarify the observations in regions where the Rydberg levels built on the ground state X (2)Sigma(+) of the ion interact with valence states of (1)Sigma(+) and (1)Pi symmetry. Previous observations of the 3ssigma, B (1)Sigma(+) Rydberg state, reviewed by Tchang-Brillet [J. Chem. Phys. 96, 6735 (1992)], have been extended to energies above its avoided crossing with the repulsive part of the D-' (1)Sigma(+) valence state where resonances of varying intensities and widths have been attributed to the fully coupled 3ssigma or 4ssigma and D-' potentials, and where the B state approaches a second avoided crossing with the C-' (1)Sigma(+) valence state [Cooper and Kirby, J. Chem. Phys. 87, 424 (1987); 90, 4895 (1989); Chem. Phys. Lett. 152, 393 (1988)]. Fragments of a progression of weak and mostly diffuse bands, observed for all four isotopomers, have been assigned to the C-'<--X transition. The least-squares modeling of the 4p and 5p complexes reveals the 3ppi, E (1)Pi Rydberg state to be one of the perturbers, violating the Deltav=0 selection rule for Rydberg-Rydberg interactions on account of its rapid transition with increasing v from Rydberg to valence state. A second (1)Pi perturber, very loosely bound and clearly of valence type, contributes to the confusion in the published literature surrounding the 5p, v=0 complex. (C) 2004 American Institute of Physics.