Intermolecular potential energy surfaces and spectra of Ne-HCN complex from ab initio calculations

Ab initio calculations of five two-dimensional intermolecular potential ene rgy surfaces of the Ne-HCN dimer have been performed using the symmetry-ada pted perturbation theory and the supermolecular method at different levels of electron correlation. A basis set of spdf-symmetry orbitals (including m idbond functions) was used. HCN was assumed linear with interatomic distanc es fixed at their vibrationally averaged <r(-2)> (-1/2) values. Fits to all calculated potential energy surfaces were obtained in the form of angular expansions incorporating the ab initio asymptotic coefficients. It has been found that high-order correlation effects are very important for Ne-HCN an d contribute about 20% to the well depth. All of the five surfaces feature a global minimum at the linear Ne-HCN geometry and a narrow and relatively flat valley surrounding HCN. Rovibrational calculations on the surfaces yie lded rotational spectra and a rotational constant whose relative difference s from their experimental counterparts range from 2% to 12% depending on th e method used to obtain the surface. This large sensitivity of spectral qua ntities to relatively modest differences between the potentials is related to the unusual shape of the potential well. (C) 2001 American Institute of Physics.