Weakly-bound clusters of atmospheric molecules: infrared spectra and structural calculations of (CO2_2)n_n-(CO)m_m-(N2_2)p_p, (n,m,p)(n, m, p) = (2, 1, 0), (2, 0, 1), (1, 2, 0), (1, 0, 2), (1, 1, 1), (1, 3, 0), (1, 0, 3), (1, 2, 1), (1, 1, 2)

preprint2022arXivOpen access

Abstract

Structural calculations and high-resolution infrared spectra are reported for trimers and tetramers containing CO2_2 together with CO and/or N2_2. Among the 9 clusters studied here, only (CO2_2)2_2-CO was previously observed by high-resolution spectroscopy. The spectra, which occur in the region of the ν3ν_3 fundamental of CO2_2 (~2350 cm−1^{-1}), were recorded using a tunable optical parametric oscillator source to probe a pulsed supersonic slit jet expansion. The trimers (CO2_2)2_2-CO and (CO2_2)2_2-N2_2 have structures in which the CO or N2_2 is aligned along the symmetry axis of a staggered side-by-side CO2_2 dimer unit. The observation of two fundamental bands for (CO2_2)2_2-CO and (CO2_2)2_2-N2_2 shows that this CO2_2 dimer unit is non-planar, unlike (CO2_2)2_2 itself. For the trimers CO2_2-(CO)2_2 and CO2_2-(N2_2)2_2, the CO or N2_2 monomers occupy equivalent positions in the 'equatorial plane' of the CO2_2, pointing toward its C atom. To form the tetramers CO2_2-(CO)3_3 and CO2_2-(N2_2)3_3, a third CO or N2_2 monomer is then added off to the 'side' of the first two. In the mixed tetramers CO2_2-(CO)2_2-N2_2 and CO2_2-CO-(N2_2)2_2, this 'side' position is taken by N2 and not CO. In addition to the fundamental bands, combination bands are also observed for (CO2_2)2_2-CO, CO2_2-(CO)2_2, and CO2_2-(N2_2)2_2, yielding some information about their low-frequency intermolecular vibrations.

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