Rotational and fine-structure transitions between the lower rotational levels of the CH radical in its X 2 Π state have been observed in absorption in the laboratory with a tunable far-infrared (TuFIR) spectrometer. The molecules were generated in an electric discharge through a mixture of methane and carbon monoxide in helium. The experimental line widths were limited by Doppler broadening and the measurements have a 1 σ experimental uncertainty of 100 kHz. The frequencies have been used together with all previous measurements of CH in the v = 0 level of the X 2 Π electronic state to determine its molecular parameters and to predict an accurate set of rotational transition frequencies.
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Davidson et al. (2001) studied this question.
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