Extreme ultraviolet laser spectroscopy on CO in the 91–100 nm range

15 November 1992

journal article
research article
Published by AIP Publishing in The Journal of Chemical Physics

Vol. 97 (10) , 7160-7166
https://doi.org/10.1063/1.463540

Abstract

Transitions from the ground state X1SIGMA+ v = 0 to eleven highly-excited states of CO were investigated using extreme ultraviolet laser spectroscopy. Excited states were detected using a two-photon ionization scheme. Improved values of band origins could be deduced from an absolute calibration of the extreme ultraviolet laser radiation against the I2 standard in the visible wavelength region. Accurate predissociation rates followed from linewidth analyses of individual rotational lines.

This publication has 15 references indexed in Scilit:

A model of the B 1Σ+–D ′ 1Σ+ Rydberg–valence predissociating interaction in the CO molecule
The Journal of Chemical Physics, 1992
XUV-laser spectroscopy on CO: isotope-selective predissociation rates
Journal de Physique II, 1992
High Rydberg states of carbon monoxide (n .gtoreq. 8) as studied by triple-resonant multiphoton ionization
The Journal of Physical Chemistry, 1991
High-resolution absorption cross sections of carbon monoxide bands at 295 K between 91.7 and 100.4 nanometers
The Astrophysical Journal, 1991
2+1 resonantly enhanced multiphoton ionization of CO via the E 1Π–X 1Σ+ transition: From measured ion signals to quantitative population distributions
The Journal of Chemical Physics, 1990
Optogalvanic observation of the CO W 1Π–B 1∑+ transition
The Journal of Chemical Physics, 1989
The photodissociation and chemistry of interstellar CO
The Astrophysical Journal, 1988
Optogalvanic spectrum of CO. II. The rotational structure of the L 1Π state
The Journal of Chemical Physics, 1988
Photoabsorption and photodissociation cross sections of CO between 88.5 and 115 nm
Chemical Physics, 1987
Two-step vacuum-ultraviolet visible excitation spectroscopy on the CO molecule
Journal of the Optical Society of America B, 1985