Probing colossal carbon rings

Samuel J. P. Marlton, Jack T. Buntine, Patrick Watkins, Chang Liu, Ugo Jacovella, Eduardo Carrascosa, James N. Bull, Evan J. Bieske

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5 Citations (Scopus)
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Abstract

Carbon aggregates containing between 10 and 30 atoms preferentially arrange themselves as planar rings. To learn more about this exotic allotrope of carbon, electronic spectra are measured for even cyclo[n]carbon radical cations (C14+
–C36+) using two-color photodissociation action spectroscopy. To eliminate spectral contributions from other isomers, the target cyclo[n]carbon radical cations are isomer-selected using a drift tube ion mobility spectrometer prior to spectroscopic interrogation. The electronic spectra exhibit sharp transitions spanning the visible and near-infrared spectral regions with the main absorption band shifting progressively to longer wavelength by ≈100 nm for every additional two carbon atoms. This behavior is rationalized with a Hückel theory model describing the energies of the in-plane and out-of-plane π orbitals. Photoexcitation of smaller carbon rings leads preferentially to neutral C3 and C5 loss, whereas rings larger than C24+ tend to also decompose into two smaller rings, which, when possible, have aromatic stability. Generally, the observed charged photofragments correspond to low energy fragment pairs, as predicted by density functional theory calculations (CAM-B3LYP-D3(BJ)/cc-pVDZ). Using action spectroscopy it is confirmed that C14+ and C18+ photofragments from C28+ rings have cyclic structures.
Original languageEnglish
Pages (from-to)1168-1178
Number of pages11
JournalThe Journal of Physical Chemistry A
Volume127
Issue number5
Early online date26 Jan 2023
DOIs
Publication statusPublished - 9 Feb 2023

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