Abstract

Time- and frequency-selective excitation spectroscopy has been demonstrated on electronic transitions from the A, B, C, and D states of the NO molecule and has been used for separating overlapping electronic systems. Using a tunable, narrow-band, coherent VUV source, laser-induced fluorescence from individual rotational vibrational levels of the NO molecule has been measured and is shown to be in good agreement with theory.

© 1985 Optical Society of America

Fluorescence-detected Raman-optical double-resonance spectroscopy of glyoxal vapor

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Two-step vacuum-ultraviolet visible excitation spectroscopy on the CO molecule

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Modulated-gain spectrometer

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