| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5415290 | Journal of Molecular Spectroscopy | 2010 | 4 Pages |
Abstract
The most stable conformer of chiral 1-(2-fluorophenyl)-1-ethanol is stabilized by a O-Hâ¯Ï interaction and it is at least 1 kcal/mol more stable than the remaining conformers. This is the result of a free jet millimeter-wave absorption spectroscopy investigation of the rotational spectra of the most abundant and O-d isotopic species.
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Authors
Shouyuan Tang, Walther Caminati,