Electronic and vibrational spectroscopy of benzonitrile cation for astrochemical consideration

The electronic and vibrational spectra of benzonitrile cation, C6H5CN+ (BZN+), in the gas phase at low temperatures are reported. Measurements were carried out using a cryogenic ion trapping apparatus. The mid-infrared spectrum shows a strong CN stretch at 2130 ± 1 cm-1 (4.694 ± 0.002 µm). The electronic spectrum is reported in the range 5040-5750 Å. This covers the forbidden B2B2 ← X2B1 and allowed C2B1 ← X2B1 transitions. The spectrum is dominated by a broad absorption feature at wavelengths shorter than 5250 Å, with the strongest absorption located at 5140 Å. Experimental data are complemented with quantum chemical calculations carried out at the density functional theory and extended multi-configurational quasi-degenerate perturbation theory level. The spectroscopic results are discussed in the context of astronomical observations in the infrared and visible.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2024-08-15
DOI
https://doi.org/10.1063/5.0223270
Citations
7
Primary Topic
Molecular Spectroscopy and Structure
Type
article
Field-Weighted Citation Impact
1.69

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article

Electronic and vibrational spectroscopy of benzonitrile cation for astrochemical consideration

E. K. Campbell, Cate S. Anstöter, Julianna Palotás, Francis C. Daly et al.
7 citations
The Journal of Chemical Physics
Molecular Spectroscopy and Structure
1.69
article

Electronic and vibrational spectroscopy of benzonitrile cation for astrochemical consideration

E. K. Campbell, Cate S. Anstöter, Julianna Palotás, Francis C. Daly, Thomas E. Douglas-Walker, A. Zheng
article en
7 citations

Abstract

The electronic and vibrational spectra of benzonitrile cation, C6H5CN+ (BZN+), in the gas phase at low temperatures are reported. Measurements were carried out using a cryogenic ion trapping apparatus. The mid-infrared spectrum shows a strong CN stretch at 2130 ± 1 cm-1 (4.694 ± 0.002 µm). The electronic spectrum is reported in the range 5040-5750 Å. This covers the forbidden B2B2 ← X2B1 and allowed C2B1 ← X2B1 transitions. The spectrum is dominated by a broad absorption feature at wavelengths shorter than 5250 Å, with the strongest absorption located at 5140 Å. Experimental data are complemented with quantum chemical calculations carried out at the density functional theory and extended multi-configurational quasi-degenerate perturbation theory level. The spectroscopic results are discussed in the context of astronomical observations in the infrared and visible.

The Journal of Chemical PhysicsVol. 161(7)
University of Edinburgh (GB)
Royal Society, University of Edinburgh, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 17%
Molecular Spectroscopy and Structure
1.69
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