Details
| Original language | English |
|---|---|
| Pages (from-to) | 4460-4464 |
| Number of pages | 5 |
| Journal | Physical Chemistry Chemical Physics |
| Volume | 9 |
| Issue number | 32 |
| Publication status | Published - 2007 |
Abstract
The rotational spectra of normal and O-d species of the two most stable conformers of chiral 1-phenyl-1-propanol, obtained by free jet millimetre-wave absorption spectroscopy reveal that both conformers are stabilized by a O-H⋯π interaction, and have the Cα-Cβ-bond oriented nearly perpendicular to the plane of the benzene ring. The methyl group is trans with respect to the phenyl group for the most stable conformer (T), while it is gauche with respect to the phenyl group and entgegen with respect to the hydroxyl group for the second most stable conformer (GE). The energy difference (EGE - ET) was estimated to be 50(50) cm-1 from relative intensity measurements.
ASJC Scopus subject areas
- Physics and Astronomy(all)
- General Physics and Astronomy
- Chemistry(all)
- Physical and Theoretical Chemistry
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In: Physical Chemistry Chemical Physics, Vol. 9, No. 32, 2007, p. 4460-4464.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Conformational preferences of chiral molecules
T2 - Free jet rotational spectrum of 1-phenyl-1-propanol
AU - Giuliano, Barbara M.
AU - Ottaviani, Paolo
AU - Favero, Laura B.
AU - Caminati, Walther
AU - Grabow, Jens Uwe
AU - Giardini, Anna
AU - Satta, Mauro
PY - 2007
Y1 - 2007
N2 - The rotational spectra of normal and O-d species of the two most stable conformers of chiral 1-phenyl-1-propanol, obtained by free jet millimetre-wave absorption spectroscopy reveal that both conformers are stabilized by a O-H⋯π interaction, and have the Cα-Cβ-bond oriented nearly perpendicular to the plane of the benzene ring. The methyl group is trans with respect to the phenyl group for the most stable conformer (T), while it is gauche with respect to the phenyl group and entgegen with respect to the hydroxyl group for the second most stable conformer (GE). The energy difference (EGE - ET) was estimated to be 50(50) cm-1 from relative intensity measurements.
AB - The rotational spectra of normal and O-d species of the two most stable conformers of chiral 1-phenyl-1-propanol, obtained by free jet millimetre-wave absorption spectroscopy reveal that both conformers are stabilized by a O-H⋯π interaction, and have the Cα-Cβ-bond oriented nearly perpendicular to the plane of the benzene ring. The methyl group is trans with respect to the phenyl group for the most stable conformer (T), while it is gauche with respect to the phenyl group and entgegen with respect to the hydroxyl group for the second most stable conformer (GE). The energy difference (EGE - ET) was estimated to be 50(50) cm-1 from relative intensity measurements.
UR - http://www.scopus.com/inward/record.url?scp=34547923168&partnerID=8YFLogxK
U2 - 10.1039/b705114j
DO - 10.1039/b705114j
M3 - Article
AN - SCOPUS:34547923168
VL - 9
SP - 4460
EP - 4464
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
SN - 1463-9076
IS - 32
ER -