High Revolution Raman UV Optical Resonance Spectra and the State-to-State Rotational Energy Transfer Rates Study of C2H2(\widetildeX1Σg+,v2"=1)
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Abstract
Using high resolution Raman UV optical resonance spectra of C2H2(\widetildeX1Σg+,v″2=1), the rotation-vibration Raman shifts in the Q(3) and Q(5) branchs of the v″2 band have been achieved for the first time. They are (1974.252±0.019)cm-1 for Q(3), (1974.127±0.008)cm-1 for Q(5). Under C2H2/C2H2 lower collision number Z experimental condition, the R-R deactivation rate constants for (v″2=1, J″=3、5、9、11、13) and the multiquanta R-R energy transfer activation rate constants from the initial pumped levels to other different rotational states (v″2=1, J″=1、3、5……15) have been extracted. The computer simulation of the experimental data has been achieved by rate constant matrix model and the simulation is in good accord with the experimental result.
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