High-resolution double resonance action spectroscopy in ion traps: vibrational and rotational fingerprints of CH2NH2+
Author(s) -
Charles R. Markus,
Sven Thorwirth,
Oskar Asvany,
Stephan Śchlemmer
Publication year - 2019
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/c9cp05487a
Subject(s) - ion , spectroscopy , resonance (particle physics) , resolution (logic) , atomic physics , chemistry , analytical chemistry (journal) , physics , organic chemistry , quantum mechanics , chromatography , artificial intelligence , computer science
By applying various action spectroscopic techniques in a 4 K cryogenic ion trap instrument, protonated methanimine, CH2NH2+, has been investigated by high-resolution rovibrational and pure rotational spectroscopy for the first time. In total, 39 rovibrational transitions within the fundamental band of the ν2 symmetric C-H stretch were measured around 3026 cm-1, which were used to predict pure rotational transition frequencies of CH2NH2+ in the ground vibrational state. Based on these predictions, nine rotational transitions were observed between 109 and 283 GHz using a novel double resonance method, which significantly improved the sensitivity of the rotational measurements. This double resonance method consists of rotational excitation followed by vibrational excitation, which is finally detected as a dip in the number of CH2NH2+-He complexes formed in the 4 K He bath of the trap. The new measurements and the derived predictions of pure rotational transitions will enable the first radio-astronomical search for CH2NH2+.
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