15min:

SEAN A. PEEBLES, REBECCA A. PEEBLES, (Present address: Department of Chemistry, Eastern Illinois University, Charleston, IL 61920), Department of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055; ROBERT L. KUCZKOWSKI AND FAITH C. BOMAN, Department of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055; MARIA EUGENIA SANZ, SONIA ANTOLÍNEZ, JOSÉL. ALONSO AND JUAN C. LÓPEZ, Departamento de Química Física, Facultad de Ciencias, Universidad de Valladolid, 47005, Valladolid, Spain; ELFI KRAKA AND DIETER CREMER, Department of Theoretical Chemistry, Göteborg University, S-41320 Göteborg, Reutersgatan 2, Sweden.

The structure of the fluorobenzene-HCl complex has been studied by Fourier-transform microwave spectroscopy and ab initio calculations. Rotational constants for three isotopomers (C₆H₅F-H³⁵Cl, C₆H₅F-H³⁷Cl and C₆D₅F-H³⁵Cl) are consistent with a -hydrogen bonded structure with the HCl located above the fluorobenzene ring, near the ring center, and the H atom of HCl pointing towards the -cloud of the ring. Two structures are consistent with the inertial data, one with the HCl almost perpendicular to the ring and the other with the H pointing toward the fluorine end of the ring. Ab initio calculations at the MP2/6-311++G(2df,2pd) level (+ BSSE corrections) were carried out to obtain difference electron density plots and indicate that the HCl is tilted by about 14^\circ from perpendicular, with the H atom toward the para carbon atom (where the -density is significantly higher). An internal semi-circular libration of the H atom is possible, leading to an average inclination angle of about 0.7^\circ, in reasonable agreement with the first of the two possible experimental structures. The calculations indicate that the bonding in the fluorobenzene-HCl complex is primarily electrostatic in nature with about 5.5 melectron transferred from the benzene ring to the HCl. Calculation of the complex binding energy at the CCSD(T)/6-311++G(2df,2pd) + CP(BSSE) level gives a value of 2.8 kcal/mole.