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Electronic spectrum of the protonated diacetylene cation (H2C4H(+)).

Identifieur interne : 000D36 ( Main/Exploration ); précédent : 000D35; suivant : 000D37

Electronic spectrum of the protonated diacetylene cation (H2C4H(+)).

Auteurs : Katherine J. Catani [Australie] ; Giel Muller [Australie] ; Pavol Jusko [Allemagne] ; Patrice Theulé [France] ; Evan J. Bieske [Australie] ; Christophe Jouvet [France]

Source :

RBID : pubmed:28863531

Abstract

The B̃(1)A1←X̃(1)A1 electronic band system of the protonated diacetylene cation (H2C4H(+)) is measured over the 230-295 nm range by photodissociating H2C4H(+) ions stored in a cryogenic ion trap and by photodissociating H2C4H(+) tagged with Ar and N2 in a tandem mass spectrometer. The B̃(1)A1←X̃(1)A1 band system has an origin at 34 941 cm(-1) for H2C4H(+), 34 934 cm(-1) for H2C4H(+)-Ar, and 34 920 cm(-1) for H2C4H(+)-N2. The spectra of H2C4H(+), H2C4H(+)-Ar, and H2C4H(+)-N2 display similar vibronic structure, which is assigned using ab initio calculations to progressions in two symmetric a1 C-C stretch vibrational modes (ν6 and ν4), with band spacings of 860 and 1481 cm(-1), respectively.

DOI: 10.1063/1.4990572
PubMed: 28863531


Affiliations:


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<div type="abstract" xml:lang="en">The B̃(1)A1←X̃(1)A1 electronic band system of the protonated diacetylene cation (H2C4H(+)) is measured over the 230-295 nm range by photodissociating H2C4H(+) ions stored in a cryogenic ion trap and by photodissociating H2C4H(+) tagged with Ar and N2 in a tandem mass spectrometer. The B̃(1)A1←X̃(1)A1 band system has an origin at 34 941 cm(-1) for H2C4H(+), 34 934 cm(-1) for H2C4H(+)-Ar, and 34 920 cm(-1) for H2C4H(+)-N2. The spectra of H2C4H(+), H2C4H(+)-Ar, and H2C4H(+)-N2 display similar vibronic structure, which is assigned using ab initio calculations to progressions in two symmetric a1 C-C stretch vibrational modes (ν6 and ν4), with band spacings of 860 and 1481 cm(-1), respectively.</div>
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