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

被引:43
作者
Murdachaew, G [1 ]
Misquitta, AJ [1 ]
Bukowski, R [1 ]
Szalewicz, K [1 ]
机构
[1] Univ Delaware, Dept Phys & Astron, Newark, DE 19716 USA
关键词
D O I
10.1063/1.1331101
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ab initio calculations of five two-dimensional intermolecular potential energy surfaces of the Ne-HCN dimer have been performed using the symmetry-adapted perturbation theory and the supermolecular method at different levels of electron correlation. A basis set of spdf-symmetry orbitals (including midbond functions) was used. HCN was assumed linear with interatomic distances 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 and 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 yielded rotational spectra and a rotational constant whose relative differences from their experimental counterparts range from 2% to 12% depending on the method used to obtain the surface. This large sensitivity of spectral quantities to relatively modest differences between the potentials is related to the unusual shape of the potential well. (C) 2001 American Institute of Physics.
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页码:764 / 779
页数:16
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