Weak hydrogen bond topology in 1,1-difluoroethane dimer: A rotational study

• Published in: The Journal of chemical physics 2017-09, Vol.147 (9), p.094301-094301
• Main Authors: Chen, Junhua, Zheng, Yang, Wang, Juan, Feng, Gang, Xia, Zhining, Gou, Qian
• Format: Article
• Language: English
• Subjects: Bonding strength; Difluoroethane; Dimers; Energy gap; Fourier transforms; Hydrogen bonds; Isomers; Physics; Rotational spectra
• ISSN: 0021-9606; 1089-7690
• DOI: 10.1063/1.4994865

The rotational spectrum of the 1,1-difluoroethane dimer has been investigated by pulsed-jet Fourier transform microwave spectroscopy. Two most stable isomers have been detected, which are both stabilized by a network of three C—H⋯F—C weak hydrogen bonds: in the most stable isomer, two difluoromethyl C—H groups and one methyl C—H group act as the weak proton donors whilst in the second isomer, two methyl C—H groups and one difluoromethyl C—H group act as the weak proton donors. For the global minimum, the measurements have also been extended to its four 13C isotopologues in natural abundance, allowing a precise, although partial, structural determination. Relative intensity measurements on a set of μ a-type transitions allowed estimating the relative population ratio of the two isomers as N I/N II ∼ 6/1 in the pulsed jet, indicating a much larger energy gap between these two isomers than that expected from ab initio calculation, consistent with the result from pseudo-diatomic dissociation energies estimation.