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      Isomer-Specific Two-Color Double-Resonance IR 2MS 3 Ion Spectroscopy Using a Single Laser: Application in the Identification of Novel Psychoactive Substances

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          Abstract

          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 2MS 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 2MS 3 and enhances its application in fields employing analytical MS. In this work, we demonstrate the methodology by acquiring single-laser IR 2MS 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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          Protomers of benzocaine: solvent and permittivity dependence.

          The immediate environment of a molecule can have a profound influence on its properties. Benzocaine, the ethyl ester of para-aminobenzoic acid that finds an application as a local anesthetic, is found to adopt in its protonated form at least two populations of distinct structures in the gas phase, and their relative intensities strongly depend on the properties of the solvent used in the electrospray ionization process. Here, we combine IR-vibrational spectroscopy with ion mobility-mass spectrometry to yield gas-phase IR spectra of simultaneously m/z and drift-time-resolved species of benzocaine. The results allow for an unambiguous identification of two protomeric species: the N- and O-protonated forms. Density functional theory calculations link these structures to the most stable solution and gas-phase structures, respectively, with the electric properties of the surrounding medium being the main determinant for the preferred protonation site. The fact that the N-protonated form of benzocaine can be found in the gas phase is owed to kinetic trapping of the solution-phase structure during transfer into the experimental setup. These observations confirm earlier studies on similar molecules where N- and O-protonation have been suggested.
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            The Free-Electron-Laser user facility FELIX

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              Infrared ion spectroscopy in a modified quadrupole ion trap mass spectrometer at the FELIX free electron laser laboratory.

              We report on modifications made to a Paul-type quadrupole ion trap mass spectrometer and discuss its application in infrared ion spectroscopy experiments. Main modifications involve optical access to the trapped ions and hardware and software coupling to a variety of infrared laser sources at the FELIX infrared free electron laser laboratory. In comparison to previously described infrared ion spectroscopy experiments at the FELIX laboratory, we find significant improvements in efficiency and sensitivity. Effects of the trapping conditions of the ions on the IR multiple photon dissociation spectra are explored. Enhanced photo-dissociation is found at lower pressures in the ion trap. Spectra obtained under reduced pressure conditions are found to more closely mimic those obtained in the high-vacuum conditions of an Fourier transform ion cyclotron resonance mass spectrometer. A gas-mixing system is described enabling the controlled addition of a secondary gas into helium buffer gas flowing into the trap and allows for ion/molecule reactions in the trap. The electron transfer dissociation (ETD) option of the mass spectrometer allows for IR structure characterization of ETD-generated peptide dissociation products.
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                Author and article information

                Journal
                Anal Chem
                Anal Chem
                ac
                ancham
                Analytical Chemistry
                American Chemical Society
                0003-2700
                1520-6882
                20 January 2021
                02 February 2021
                : 93
                : 4
                : 2687-2693
                Affiliations
                []FELIX Laboratory, Institute for Molecules and Materials, Radboud University , Toernooiveld 7, 6525 ED Nijmegen, The Netherlands
                []Forensic Laboratory, Unit Amsterdam, Dutch National Police , Kabelweg 25, 1014 BA Amsterdam, The Netherlands
                [§ ]Van’t Hoff Institute for Molecular Sciences, University of Amsterdam , P.O. Box 94157, 1090 GD Amsterdam, The Netherlands
                []Co van Ledden Hulsebosch Center (CLHC), Amsterdam Center for Forensic Science and Medicine , P.O. Box 94157, 1090 GD Amsterdam, The Netherlands
                Author notes
                [* ]Email: g.berden@ 123456science.ru.nl . Phone: +31 243653951.
                Article
                10.1021/acs.analchem.0c05042
                7859929
                33470107
                1fa52698-376e-4408-9fbb-9f6025cd1946
                © 2021 The Authors. Published by American Chemical Society

                This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License, which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.

                History
                : 01 December 2020
                : 12 January 2021
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                ac0c05042
                ac0c05042

                Analytical chemistry
                Analytical chemistry

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