Abstract
Pure rotational spectroscopy of the FeCl radical (X 6Δi) has been carried out using millimeter/sub-millimeter direct absorption techniques. The species was created by the reaction of chlorine with iron vapor. All six spin - orbit components were observed in the majority of the twenty-one rotational transitions recorded. Chlorine hyperfine structure was resolved in the Ω = 9/2 and 7/2 components, and lambda-type doubling observed in the Ω = 3/2, 1/2, and - 1/2 ladders. The data were analyzed with a 6Δ Hamiltonian, and rotational, fine structure, lambda-doubling, and hyperfine parameters determined. The hyperfine and lambda-doubling interactions in FeCl appear to be different from those in the FeF radical.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 517-526 |
| Number of pages | 10 |
| Journal | Chemical Physics Letters |
| Volume | 270 |
| Issue number | 5-6 |
| DOIs | |
| State | Published - May 30 1997 |
ASJC Scopus subject areas
- General Physics and Astronomy
- Physical and Theoretical Chemistry
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