Premium
SPECIAL FEATURE: TUTORIAL Slow Heating Methods in Tandem Mass Spectrometry
Author(s) -
McLuckey Scott A.,
Goeringer Douglas E.
Publication year - 1997
Publication title -
journal of mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 1076-5174
DOI - 10.1002/(sici)1096-9888(199705)32:5<461::aid-jms515>3.0.co;2-h
Subject(s) - chemistry , mass spectrometry , dissociation (chemistry) , ion , infrared multiphoton dissociation , quadrupole ion trap , ion trap , ion trapping , tandem mass spectrometry , kinetic energy , analytical chemistry (journal) , atomic physics , chromatography , physics , organic chemistry , quantum mechanics
Several approaches to ion activation in tandem mass spectrometry have been developed in recent years for use in ion trapping instruments that allow for conditions to be reached wherein rates of ion activation and deactivation are comparable. These approaches are defined as slow heating methods and include continuous‐wave laser infrared multiphoton dissociation, dissociation driven by blackbody radiation, quadrupole ion trap collisional activation and sustained off‐resonance irradiation in ion cyclotron resonance mass spectrometry. In the limiting case in which ion activation and deactivation rates are equal, a steady‐state parent ion internal energy distribution is achieved and the kinetics of dissociation can be interpreted in analogy with thermal dissociation. This discussion describes the thermal analogy and the limiting conditions of rapid energy exchange and slow energy exchange along with the possible ramifications for dissociation rates and product ion spectra. The figures of merit that the various slow heating methods share as a class of activation methods are also discussed. The purpose of this perspective is to provide a frame‐of‐reference from which slow heating methods can be considered. Such methods are seeing increasing use as the number of ion trapping instruments grows and have shown remarkable success with dissociation of high‐mass ions. © 1997 by John Wiley & Sons, Ltd.