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.
S. Tang, W. Caminati (2010). Free jet rotational spectrum of the most stable conformer of 1-(2-fluorophenyl)-1-ethanol. JOURNAL OF MOLECULAR SPECTROSCOPY, 260, 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:
Eventuali allegati, non sono esposti
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
