Analysis of high excited "hot" bands of the SO2 molecule

The main goal of the present study is to analyse rotational structures of highly excited "hot" vibrational bands, v1+2v2-v2 and 2v2+v3-v2, v2+3v3-v2 and 2v1+v2+v3-v2, and v2+2v3-v2. All of these bands are located in the region of considerably stronger bands, v1 + v2 and v2 + v3, 3v3 and 2v1+v3, and 2v3, respectively . On that reason, as the first step of analysis, we made assignments of transitions belonging to these strong bands. As the result of analysis, we were able to assign three times more transitions to the bands v1 + v2 , v2 + v3, and 3v3 (3360 transitions with Jmax. = 78 and Kmax.a = 27 to the band v1 + v2, and 2380 transitions with Jmax. = 69 and Kmax.a = 24 to the band v2 + v3, …

On the "expanded local mode" approach applied to the methane molecule

Methane (CH4 ) is one of the main prototypical hydrocarbons and is of great importance in a variety of applications ranging from our understanding of the chemical bonding, structure and quantum dynamics, reaction kinetics to geology, astrophysics, atmospheric and environmental science. On that reason, during more than five last decades both the vibrational and ro-vibrational spectra of methane were a subject of numerous studies (see, for example, M.Hippler and M.Quack, J. Chem. Phys. 116 (2002) 6045. and H.M.Niederer, S.Albert, S.Bauerecker, V.Boudon, J.P.Champion and M.Quack, Chimia 62 (2008) 273 where extensive references to spectroscopic and theoretical works can be found, the complete, …

Fermi-type interaction in molecular and atomic Hamiltonians. Application to molecular systems and Bose-Einstein condensates.

International audience; We present a simple prescription to build phenomenological Hamiltonians describing Fermi-type interactions and apply the developed formalism to two distinct physical systems. First, in a very simple way, we derive equations describing time dynamics of two coherently coupled Bose-Einstein condensates. Further, for bent XY2 molecules, we reproduce all the experimental data with an excellent precision.

On the SPGF approach in asymmetric top molecules: application to the hydrogen sulfide.