Observing the Completion of the First Solvation Shell of Carbon Dioxide in Argon from Rotationally Resolved Spectra

ABSTRACT: Widespread interest in weakly bound molecular clusters of medium size (5-50 molecules) is motivated by their complicated energy landscapes, which lead to hundreds or thousands of distinct isomers. But most studies are theoretical in nature, and there are no experimental results which provide definitive structural information on completion of the first solvation shell. Here we assign rotationally resolved mid-infrared spectra to argon clusters containing a single carbon dioxide molecule, CO2-Ar15 and CO2-Ar17. These mark the completion of the first solvation shell for CO2 in argon. The assignments are confirmed by nuclear spin intensity alternation in the spectra, a marker of highly symmetric structures for these clusters. Precise values are determined for rotational parameters and for shifts of the CO2 vibrational frequency induced by the argon atoms. The spectra indicate possible lowfrequency (similar to 2 cm-1) vibrational modes in these clusters, posing a challenge for future cluster theory.

Automated summary

This study provides experimental evidence for the structural information of the first solvation shell of carbon dioxide in argon clusters, and discovers possible low-frequency vibrational modes, posing a challenge for cluster theory.