Ion‐molecule reactions of mass‐selected ions

Abstract

Gas‐phase reactions of mass‐selected ions with neutrals covers a very broad area of fundamental and applied mass spectrometry (MS). Oftentimes, ion‐molecule reactions (IMR) can serve as a viable alternative to collision‐induced dissociation and other ion dissociation techniques when using tandem MS. This review focuses on the literature pertaining applications of IMR since 2013. During the past decade considerable efforts have been made in analytical applications of IMR, including advances in one of the major techniques for characterization of unsaturated fatty acids and lipids, ozone‐induced dissociation, and the development of a new technique for sequencing of large ions, hydrogen atom attachment/abstraction dissociation. Many advances have also been made in identifying gas‐phase chemistry specific to a functional group in organic and biological compounds, which are useful in structure elucidation of analytes and differentiation of isomers/isobars. With “soft” ionization techniques like electrospray ionization having become mainstream for quite some time now, the efforts in the area of metal ion catalysis have firmly moved into exploring chemistry of ligated metal complexes in their “natural” oxidation states allowing to model individual steps of mechanisms in homogeneous catalysis, especially in combination with high‐level DFT calculations. Finally, IMR continue to contribute to the body of knowledge in the area of chemistry of interstellar processes.

Probing Intermediates of Ion/Molecule Reactions by their Independent Gas‐Phase Synthesis and Fragmentation – The Thiomethoxymethyl Complexes [(bipy)M(CH2SCH3)]+ (M=Pt, Pd, Ni)

“…[6,7,[83][84][85][86] In this respect, gas phase experiments can serve as a fruitful source of serendipitous findings. [87] For example, it has previously been found that "rollover"-cyclometalated [88][89][90][91][92] [(bipyÀ H)Pt] + (1, bipy = 2,2'-bipyridine) is able to activate a variety of small molecules such as methane, [93] chloromethanes, [94] ethers, [95] and thioethers, [96,97] and all these reactions are unprecedented in solution. Particularly, in the ion/molecule reaction of [(bipyÀ H)Pt] + (1) with (CH 3 ) 2 S, [97] the elimination of C 2 H 4 (i. e. CÀ C-bond coupling of the two methyl groups of the neutral substrate) was quite unexpected (Figure 2).…”

Intramolecular Ring–Chain Equilibrium Elimination Strategy for Pinpointing C═C Positional and Geometric Isomers of N-Alkylpyridinium Unsaturated Fatty Acid Derivatives via Ion Mobility-Mass Spectrometry

“…Despite the continuous progress of chemical derivatization for UFA, there are few studies on the separation of UFA based on ion mobility-mass spectrometry (IM-MS), due to the weak separation ability and poor substrate generalization. − More methods have been developed for coupling with high-performance liquid chromatography-mass spectrometry (HPLC-MS) or gas chromatography-mass spectrometry (GC–MS). − Unlike the chromatographic-based and fragmentation-based methods, − IM-MS is expected to realize the high-throughput analysis of UFA isomers under gas-phase conditions because the conformation of the CC in UFA can significantly affect the overall molecular shape and collision cross section. Groessl et al achieved a better separation and identification of cis / trans phosphatidylcholine isomers using high-resolution, low-field multiplexed drift-tube IM-MS .…”