z-logo
open-access-imgOpen Access
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+.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom