The rotational spectrum and hyperfine structure of the methylene radical CH2 studied by far-infrared laser magnetic resonance spectroscopy

Trevor J. Sears, P. R. Bunker, A. R. W. McKellar, K. M. Evenson, D. A. Jennings, John M. Brown

The Journal of Chemical Physics · 1982 · 135 citations · 42 references

Concepts

Abstract

Thirteen pure rotational transitions of CH2 in its X̃ 3B1 ground vibronic state have been measured and assigned using the technique of far-infrared laser magnetic resonance (LMR) spectroscopy. The energy levels thus determined led to the prediction and subsequent detection by microwave spectroscopy of a further rotational transition 404–313, at lower frequency (∼70 GHz). The analysis of these observations yields precise rotational constants as well as spin–spin, spin-rotation, and hyperfine interaction parameters for gas phase CH2. Its rotational spectrum may enable interstellar CH2 to be detected by radio astronomy. Two rotaional transitions within the v1=1 excited vibrational state have also been identified in the LMR spectrum. Future observations of vibrationally excited CH2 may afford a means of determining the singlet–triplet splitting in methylene, and studies of CD2 and CHD will result in improved structural determinations.

References

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