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Phys Chem Chem Phys. 2017 May 17;19(19):12221-12228. doi: 10.1039/c7cp01666b.

Tunnelling and barrier-less motions in the 2-fluoroethanol-water complex: a rotational spectroscopic and ab initio study.

Author information

1
Department of Chemistry, University of Alberta, 11227 Saskatchewan Drive, Edmonton, Alberta T6G 2G2, Canada. Yunjie.xu@ualberta.ca.

Abstract

The pure rotational spectrum of the 2-fluoroethanol (2-FE)water complex was measured using a chirped pulse Fourier-transform microwave spectrometer and a cavity-based Fourier-transform microwave spectrometer. In the detected 2-FEwater conformer, 2-FE serves as a proton donor, in contrast to its role in the observed ethanolwater conformer, while water acts simultaneously as a hydrogen bond donor and acceptor, forming a hydrogen-bonded ring with an OHO and an OHF hydrogen bond. Comparison to the calculated dipole moment components suggests that the observed structure sits between the two most stable minima identified theoretically. This conclusion is supported by extensive deuterium isotopic data. Further analysis shows that these two minima are connected by a barrier-less wagging motion of the non-bonded hydrogen of the water subunit. The observed narrow splitting with a characteristic 3 : 1 intensity ratio is attributed to an exchange of the bonded and non-bonded hydrogen atoms of water. The tunneling barrier of a proposed tunneling path is calculated to be as low as 5.10 kJ mol-1. A non-covalent interaction analysis indicates that the water rotation motion along the tunneling path has a surprisingly small effect on the interaction energy between water and 2-FE.

PMID:
28451670
DOI:
10.1039/c7cp01666b

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