Beyond the flask: Reactions on the fly in ambient mass spectrometry

•We review chemical reactions associated with ambient ionization mass spectrometry.•Ambient ionization reactions improve analytical sensitivity.•Ambient ionization reactions elucidate mechanisms of reactions.•Ambient ionization reactions may be used to perform rapid preparative chemistry.•Ambient io...

Full description

Saved in:
Bibliographic Details
Published inTrAC, Trends in analytical chemistry (Regular ed.) Vol. 57; pp. 135 - 146
Main Authors Espy, Ryan D., Wleklinski, Michael, Yan, Xin, Cooks, R. Graham
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.05.2014
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:•We review chemical reactions associated with ambient ionization mass spectrometry.•Ambient ionization reactions improve analytical sensitivity.•Ambient ionization reactions elucidate mechanisms of reactions.•Ambient ionization reactions may be used to perform rapid preparative chemistry.•Ambient ionization enables in situ reactions rapidly, directly on native samples. Ionic reactions in bulk solution generally occur relatively slowly, and the course of reaction can be followed by on-line monitoring using, for example, electrospray ionization mass spectrometry (MS). In another approach, ionic reactions occurring in confined volumes can be studied with a focus on increasing reaction rates upon reduction in solution volume (e.g., by solvent evaporation from small droplets). Such a situation is encountered in ambient ionization MS, which involves the ionization of samples in their native state without significant sample preparation. Reagents can be included in the spray solvents used in ambient ionization and rapid derivatization reactions can accompany ionization. These latter experiments form the topic of this review. Emphasis is on their value in chemical analysis, but the products of these reactions can also be collected easily and form the basis for small-scale synthesis.
ISSN:0165-9936
1879-3142
DOI:10.1016/j.trac.2014.02.008