ISSN:
1089-7690
Source:
AIP Digital Archive
Topics:
Physics
,
Chemistry and Pharmacology
Notes:
The two-dimensional interaction potential of the N+2(X 2Σ+g) –He(X 1S) system has been calculated using highly correlated ab initio MCSCF-CI wave functions for a fixed value of the N+2 bond length (2.110 a0). It is found to have a minimum about 140 cm−1 below the N+2 +He dissociation limit, significantly deeper than the minimum in the neutral system N2–He. This well depth is enough to give rise to a cluster-like, bound structure with a considerable number of vibration–rotation levels in the electronic ground state. The well depth is almost independent of the N2–He angle, which leads to large amplitude bending motions. Rovibrational calculations have been performed on the surface for J=0, 1, and 2. Values for the rotational constant B, the fundamental stretching frequency νs, and its first and second overtones, and the rotational constant Cn in each nνs manifold, have been obtained from the energy levels computed. It is found that B=1.879 cm−1, 1νs =55.231 cm−1, 2νs =83.404 cm−1, 3νs =92.491 cm−1, C0=0.477 cm−1, C1=0.370 cm−1, and C2=0.254 cm−1. Estimates of the accuracy of these parameters are made.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1063/1.455062
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