Answers are grounded in this paper and cite their sources.
With the help of a microwave Fourier transform spectrometer in the range from 18 GHz to 26 GHz, the coefficients ß for the linear pressure depedence of collisional dephasing rates 1/T2 have been determined by the transient emission technique for fourteen pure rotational transitions of SO2 with 5 ≦ J' ≦ 66 in the ground vibrational state, twelve transitions with 8 ≦ J' ≦ 62 in the first excited bending vibrational state, and twelve transitions of methanol with 2 ≦ J' ≦ 11, where J' is the rotational quantum number of the upper level of a transition. The T2-parameter ß for the transition J(K-, K+) - 49(4, 46 ) - 48(5, 43) of SO2 in the ground state shows an anomalous behaviour, whereas the values for all other transitions show a J-dependence in accordance with previous results. No significant variation of T2-parameters with J has been found for the rotational transitions of CH3OH.
No takes yet. Share an insight, caveat, or question.
Mehrotra et al. (1985) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: