15min:

J. DEMAISON, F. WILLAERT, Laboratoire PhLAM, CNRS, Université de Lille I, Bat. P5, 59655 Villeneuve d'Ascq Cedex, France; H. MOLLENDAL, Department of Chemistry, University of Oslo, P.O. Box 1033, Blindern, NO-0315 Oslo, Norway; A. PERRIN, J. ORPHAL, Laboratoire Inter Universitaire des Systemes Atmosphériques, CNRS, Université Paris 12, 61 Av du General de Gaulle, 94010 Créteil Cedex France; H. D. RUDOLPH, Department of Chemistry, University of Ulm, 89069 Ulm, Germany.

The quadratic, cubic and semi-diagonal quartic force field of vinyl chloride has been calculated at the MP2 level of theory employing a basis set of triple-zeta quality. The spectroscopic constants derived from this force field are compared to the experimental values. To make this comparison more complete, the rotational constants of the lowest excited state, v₉= 1 have been determined by microwave spectroscopy and the ₁₂ band has been investigated by high-resolution infrared Fourier transform spectroscopy. The equilibrium structure has been derived from experimental ground state rotational constants and ab initio rovibrational interaction parameters. This semi experimental structure is in excellent agreement with the ab initio structure calculated at the CCSD(T) level of theory using a basis set of quintuple-zeta quality and a core correlation correction. The experimental mass-dependent rm structures are also determined and their accuracy is discussed.