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Differentiation of Regioisomeric Aromatic Ketocarboxylic Acids by Positive Mode Atmospheric Pressure Chemical Ionization Collision-Activated Dissociation Tandem Mass Spectrometry in a Linear Quadrupole Ion Trap Mass Spectrometer
Authors:Lucas M. Amundson  Benjamin C. Owen  Vanessa A. Gallardo  Steven C. Habicht  Mingkun Fu  Ryan C. Shea  Allen B. Mossman  Hilkka I. Kenttämaa
Affiliation:(1) Department of Chemistry, Purdue University, BRWN Building, 560 Oval Dr., West Lafayette, IN 47907, USA;(2) British Petroleum (BP), Naperville, IL 60563, USA;(3) Present address: Center for Naval Analysis, 4825 Mark Center Drive, Alexandria, VA 22311, USA;(4) Present address:  , Millennium, 40 Landsdowne Street, Cambridge, MA 02139, USA;
Abstract:Positive-mode atmospheric pressure chemical ionization tandem mass spectrometry (APCI-MS n ) was tested for the differentiation of regioisomeric aromatic ketocarboxylic acids. Each analyte forms exclusively an abundant protonated molecule upon ionization via positive-mode APCI in a commercial linear quadrupole ion trap (LQIT) mass spectrometer. Energy-resolved collision-activated dissociation (CAD) experiments carried out on the protonated analytes revealed fragmentation patterns that varied based on the location of the functional groups. Unambiguous differentiation between the regioisomers was achieved in each case by observing different fragmentation patterns, different relative abundances of ion-molecule reaction products, or different relative abundances of fragment ions formed at different collision energies. The mechanisms of some of the reactions were examined by H/D exchange reactions and molecular orbital calculations.
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