Disentangling electronic spectra of linear and cyclic hydrogenated carbon cluster cations, C2n+1H+ (n = 3–10)

Marlton, Samuel J. P., Buntine, Jack T., Liu, Chang, Watkins, Patrick, Jacovella, Ugo, Carrascosa, Eduardo, Bull, James N. ORCID: https://orcid.org/0000-0003-0953-1716 and Bieske, Evan J. (2022) Disentangling electronic spectra of linear and cyclic hydrogenated carbon cluster cations, C2n+1H+ (n = 3–10). The Journal of Physical Chemistry A, 126 (38). 6678–6685. ISSN 1089-5639

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Abstract

Electronic spectra are measured for protonated carbon clusters (C2n+1H+) containing between 7 and 21 carbon atoms. Linear and cyclic C2n+1H+ isomers are separated and selected using a drift tube ion mobility stage before being mass selected and introduced into a cryogenically cooled ion trap. Spectra are measured using a two-color resonance-enhanced photodissociation strategy, monitoring C2n+1+ photofragments (H atom loss channel) as a function of excitation wavelength. The linear C7H+, C9H+, C11H+, C13H+, C15H+, and C17H+ clusters, which are predicted to have polyynic structures, possess sharp 11Σ+ ← X̃1Σ+ transitions with well-resolved vibronic progressions in C–C stretch vibrational modes. The vibronic features are reproduced by spectral simulations based on vibrational frequencies and geometries calculated with time-dependent density functional theory (ωB97X-D/cc-pVDZ level). The cyclic C15H+, C17H+, C19H+, and C21H+ clusters exhibit weak, broad transitions at a shorter wavelength compared to their linear counterparts. Wavelengths for the origin transitions of both linear and cyclic isomers shift linearly with the number of constituent carbon atoms, indicating that in both cases, the clusters possess a common structural motif.

Item Type: Article
Faculty \ School: Faculty of Science > School of Chemistry
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Depositing User: LivePure Connector
Date Deposited: 04 Oct 2022 09:30
Last Modified: 20 Oct 2022 16:30
URI: https://ueaeprints.uea.ac.uk/id/eprint/88831
DOI: 10.1021/acs.jpca.2c05051

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