Isolation of a Halogen-Bonded Complex Formed between Methane and Chlorine Monofluoride and Characterisation by Rotational Spectroscopy and Ab Initio Calculations

A halogen-bonded complex formed between methane and chlorine monofluoride has been isolated in the gas phase before the reaction between the components and has been characterised through its rotational spectrum, which is of the symmetric-top type but only exhibits K = 0 type transitions at the low effective temperature of the pulsed-jet experiment. Spectroscopic constants for two low-lying states that result from internal rotation of the CH(4) subunit were detected for each of the two isotopic varieties H(4)C···(35)ClF and H(4)C···(37)ClF and were analysed to show that ClF lies on the symmetry axis with Cl located closer than F to the C atom, at the distance r(0)(C···Cl) [Formula: see text] Å and with an intermolecular stretching force constant k(σ) [Formula: see text] 4 N m(−1). Ab initio calculations at the explicitly correlated level CCSD(T)(F12c)/cc-pVTZ-F12 show that in the equilibrium geometry, the ClF molecule lies along a C(3) axis of CH(4) and Cl is involved in a halogen bond. The Cl atom points at the nucleophilic region identified on the C(3) axis, opposite the unique C–H bond and somewhere near the C atom and the tetrahedron face centre, with r(e)(C···Cl) = 3.191 Å. Atoms-in-molecules (AIM) theory shows a bond critical point between Cl and C, confirming the presence of a halogen bond. The energy that is required to dissociate the complex from the equilibrium conformation into its CH(4) and ClF components is only D(e) [Formula: see text] 5 kJ mol(−1). A likely path for the internal rotation of the CH(4) subunit is identified by calculations at the same level of theory, which also provide the variation of the energy of the system as a function of the motion along that path. The barrier to the motion along the path is only [Formula: see text] 20 cm(−1).