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J Chem Phys ; 141(3): 034304, 2014 Jul 21.
Article in English | MEDLINE | ID: mdl-25053317

ABSTRACT

The rotational spectra of the monoterpenoids thymol and carvacrol are reported in the frequency range 2-8.5 GHz, obtained with broadband Fourier-transform microwave spectroscopy. For carvacrol four different conformations were identified in the cold conditions of the molecular jet, whereas only three conformations were observed for thymol. The rotational constants and other molecular parameters are reported and compared with quantum chemical calculations. For both molecules, line splittings due to methyl group internal rotation were observed and the resulting barrier heights could be determined. The experimental barrier heights, 4.0863(25) kJ/mol for trans-carvacrol-A, 4.4024(16) kJ/mol for trans-carvacrol-B, and 0.3699(11) kJ/mol for trans-thymol-A, are compared with similar molecules.


Subject(s)
Microwaves , Molecular Conformation , Monoterpenes/chemistry , Spectrum Analysis , Thymol/chemistry , Cymenes , Hydrogen Bonding , Models, Molecular , Quantum Theory , Rotation , Stereoisomerism
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