Abstract
Vibrational predissociation linewidths for the CO2 dimer and trimer and the Ne–CO2 and Ar–CO2 complexes have been resolved using a bolometer-detected (optothermal) molecular-beam color-center laser spectrometer. Observations were made on the pair of vibrations near 3715 and 3613 cm−1 corresponding to the ν1+ν3/2ν02+ν3 Fermi diad of CO2. Homogeneous linewidths of from ∼0.5 to ∼22 MHz (FWHM) were measured for these related complexes, with Ne–CO2 exhibiting both the broadest and the sharpest lines for the upper and lower bands, respectively. Ar–CO2 and (CO2)2 showed mode-independent intermediate predissociation rates while only the lower band of (CO2)3 could be found. The results indicate that V→V energy transfer processes are the dominant predissociation channels with symmetry selection or propensity rules and specific resonances playing a role.
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