The most stable conformer of chiral 1-(2-fluorophenyl)-1-ethanol is stabilized by a O-H 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.
Free jet rotational spectrum of the most stable conformer of 1-(2-fluorophenyl)-1-ethanol / S. Tang; W. Caminati. - In: JOURNAL OF MOLECULAR SPECTROSCOPY. - ISSN 0022-2852. - STAMPA. - 260:(2010), pp. 120-123. [10.1016/j.jms.2010.01.007]
Free jet rotational spectrum of the most stable conformer of 1-(2-fluorophenyl)-1-ethanol
CAMINATI, WALTHER
2010
Abstract
The most stable conformer of chiral 1-(2-fluorophenyl)-1-ethanol is stabilized by a O-H 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.File in questo prodotto:
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