Isomer-Specific Two-Color Double-Resonance IR2MS3 Ion Spectroscopy Using a Single Laser: Application in the Identification of Novel Psychoactive Substances
Author(s) -
Fred A. M. G. van Geenen,
Ruben F. Kranenburg,
Arian C. van Asten,
Jonathan Martens,
Jos Oomens,
Giel Berden
Publication year - 2021
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/acs.analchem.0c05042
Subject(s) - chemistry , ion , mass spectrometry , laser , analytical chemistry (journal) , mass spectrum , spectroscopy , ion trap , context (archaeology) , population , resonance (particle physics) , atomic physics , spectral line , infrared spectroscopy , optics , physics , paleontology , demography , organic chemistry , chromatography , quantum mechanics , astronomy , sociology , biology
The capability of an ion trap mass spectrometer to store ions for an arbitrary amount of time allows the use of a single infrared (IR) laser to perform two-color double resonance IR-IR spectroscopic experiments on mass-to-charge ( m / z ) selected ions. In this single-laser IR 2 MS 3 scheme, one IR laser frequency is used to remove a selected set of isomers from the total trapped ion population and the second IR laser frequency, from the same laser, is used to record the IR spectrum of the remaining precursor ions. This yields isomer-specific vibrational spectra of the m / z -selected ions, which can reveal the structure and identity of the initially co-isolated isomeric species. The use of a single laser greatly reduces the experimental complexity of two-color IR 2 MS 3 and enhances its application in fields employing analytical MS. In this work, we demonstrate the methodology by acquiring single-laser IR 2 MS 3 spectra in a forensic context, identifying two previously unidentified isomeric novel psychoactive substances (NPS) from a sample that was confiscated by the Amsterdam Police.
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