par Lauzin, Clément 
;Didriche, Keevin ;Macko, Peter ;Demaison, Jean F.;Liévin, Jacques ;Herman, Michel
Référence The Journal of Physical Chemistry. A, 113, 11, page (2359-2365)
Publication Publié, 2009
;Didriche, Keevin ;Macko, Peter ;Demaison, Jean F.;Liévin, Jacques ;Herman, Michel Référence The Journal of Physical Chemistry. A, 113, 11, page (2359-2365)
Publication Publié, 2009
Article révisé par les pairs
| Résumé : | New theoretical and experimental results on the acetylene-Ar van der Waals complex are presented and the literature is reviewed. New ab initio calculations at the MP2 level were performed using large basis sets with diffuse functions and taking into account the basis set superposition error. It was found that the structure of acetylene is not significantly altered by the complexation and that its vibrational frequencies are only slightly lowered. Finally, it was observed that the calculated properties of the complex (structure, vibrational spectrum, bond dissociation energy) are not sensitive to the structure imposed on acetylene. Experimentally, acetylene-Ar was produced in a supersonic expansion under experimental conditions corresponding to 9 K rotational temperature. Thanks to the performances of CW-CRDS detection, the Ka = 0 ← 1, 1 ← 0, and 2 ← 1 sub- bands of the v1 + v3 band could be recorded and resolved and most of their lines assigned. Upper-state rotational constants were fitted, however not including the upper Ka = 2 state, which shows K-doubling the opposite of the expected. The Lorentzian width of most line profiles sets the mean lifetime to some 7.5 ns. Local perturbations affecting line positions and/or line widths are demonstrated. Additional series of lines tentatively attributed to acetylene-Ar are discussed.© 2009 American Chemical Society. |
