Details

Autor(en) / Beteiligte

• Xie, Fan
• Seifert, Nathan A
• Heger, Matthias
• Thomas, Javix
• Jäger, Wolfgang
• Xu, Yunjie

Titel

The rich conformational landscape of perillyl alcohol revealed by broadband rotational spectroscopy and theoretical modelling

Ist Teil von

• Physical chemistry chemical physics : PCCP, 2019-07, Vol.21 (28), p.1548-15416

Ort / Verlag

England: Royal Society of Chemistry

Erscheinungsjahr

2019

Link zum Volltext

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• The rotational spectrum of perillyl alcohol, a naturally occurring, chiral, dietary monoterpene, was investigated using a chirped pulse Fourier transform microwave spectrometer and a cavity-based Fourier transform microwave spectrometer. To aid the assignment of the dense chirped pulse spectrum obtained, extensive theoretical conformational searches were carried out. In one approach, several one and two-dimensional scans along three dihedral angles associated with the rotational motions of the -OH, -CH 2 OH, and -C(CH 2 )CH 3 groups were performed. These scans, combined with the equatorial and axial positions of the -C(CH 2 )CH 3 group, resulted in 54 conformers. The same conformers were identified in the second approach where a semi-classical conformational search code was used. The relative stabilities of the conformers and the interconversion barriers among them were explored extensively at the DFT B3LYP-D3(BJ)/def2-TZVP and B3LYP-D3(BJ)/6-311++G(2d,p), as well as local MP2/aug-cc-pVQZ levels of theory, and 12 conformers were ultimately identified as possibly observable candidates in a molecular jet expansion. Rotational spectra of eight out of the 12 candidates were observed experimentally and analyzed. The non-observation of the remaining four conformers may be attributed to their low abundances. The study points out the importance of identifying all conformers of relevant abundance, even those which could not be detected experimentally, in order to properly benchmark the theoretical relative stabilities with the experimental ones. A comprehensive study of the conformational distribution of perillyl alcohol contributes to our understanding of its structural properties which may influence its functions. We explore the conformational landscape of perillyl alcohol in order to properly account for the sources of the conformers observed.