| DOI | Trouver le DOI : https://doi.org/10.1021/acs.jpclett.2c01520 |
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| Auteur | Rechercher : Barclay, A. J.; Rechercher : McKellar, A. R. W.1; Rechercher : Moazzen-Ahmadi, N.Identifiant ORCID : https://orcid.org/0000-0001-8307-3480 |
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| Affiliation | - Conseil national de recherches du Canada. Technologies de sécurité et de rupture
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| Bailleur de fonds | Rechercher : Natural Sciences and Engineering Research Council of Canada |
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| Format | Texte, Article |
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| Sujet | cluster chemistry; cluster structure; energy levels; group theory; molecular structureshow |
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| Résumé | 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 low-frequency (∼2 cm⁻¹) vibrational modes in these clusters, posing a challenge for future cluster theory. |
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| Date de publication | 2022-07-06 |
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| Maison d’édition | American Chemical Society |
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| Dans | |
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| Langue | anglais |
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| Publications évaluées par des pairs | Oui |
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| Exporter la notice | Exporter en format RIS |
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| Signaler une correction | Signaler une correction (s'ouvre dans un nouvel onglet) |
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| Identificateur de l’enregistrement | 0caf2183-5bc5-433e-934f-59f3d928c13e |
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| Enregistrement créé | 2024-01-29 |
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| Enregistrement modifié | 2024-01-29 |
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