4.7 Article

Negative-ion field desorption revitalized by using liquid injection field desorption/ionization-mass spectrometry on recent instrumentation

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 413, Issue 27, Pages 6845-6855

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03641-9

Keywords

Field ionization; Field desorption; Liquid injection field desorption; ionization; Field emitter; Negative ions; Ionization process; Anions; Ionic liquids; Cluster ions; Soft ionization; Desorption ionization; Anionic surfactants

Funding

  1. Projekt DEAL

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Field ionization, field desorption, and liquid injection field desorption/ionization offer soft positive ionization for analytes in gaseous or condensed phase, while negative-ion mode remains rare but promising, particularly in the case of LIFDI. This study demonstrates the potential of negative-ion mode in modern mass spectrometry, showcasing successful application on a variety of compounds including ionic liquids, polymers, and anionic surfactants.
Field ionization (FI), field desorption (FD), and liquid injection field desorption/ionization (LIFDI) provide soft positive ionization of gaseous (FI) or condensed phase analytes (FD and LIFDI). In contrast to the well-established positive-ion mode, negative-ion FI or FD have remained rare exceptions. LIFDI provides sample deposition under inert conditions, i.e., the exclusion of atmospheric oxygen and water. Thus, negative-ion LIFDI could potentially be applied to highly sensitive anionic compounds like catalytically active transition metal complexes. This work explores the potential of negative-ion mode using modern mass spectrometers in combination with an LIFDI source and presents first results of the application of negative-ion LIFDI-MS. Experiments were performed on two orthogonal-acceleration time-of-flight (oaTOF) instruments, a JEOL AccuTOF GCx and a Waters Micromass Q-TOF Premier equipped with LIFDI sources from Linden CMS. The examples presented include four ionic liquids (ILs), i.e., N-butyl-3-methylpyridinium dicyanamide, 1-butyl-3-methylimidazolium tricyanomethide, 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide, and trihexyl(tetradecyl)phosphonium tris(pentafluoroethyl)trifluorophosphate), 3-(trifluoromethyl)-phenol, dichloromethane, iodine, polyethylene glycol diacid, perfluorononanoic acid, anionic surfactants, a tetraphosphazene silanol-silanolate, and two bis(catecholato)silanes. Volatile samples were delivered as vapors via the sample transfer capillary of the LIFDI probe or via a reservoir inlet. Condensed phase samples were applied to the emitter as dilute solutions via the sample transfer capillary. The compounds either yielded ions corresponding to their intact anions, A(-), or the [M-H](-) species formed upon deprotonation. This study describes the instrumental setups and the operational parameters for robust operation along with a discussion of the negative-ion LIFDI spectra of a variety of compounds.

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