| Title | Quantitatively resolving mixtures of isobaric compounds using chemical ionization mass spectrometry by modulating the reactant ion composition. | | Author(s) | Fortner EC, Knighton WB | | Institution | Department of Chemistry and Biochemistry, Montana State University - Bozeman, Bozeman, MT 59717, USA. | | Source | Rapid Commun Mass Spectrom 2008 Jul 22; 22(16):2597-2601. | | Abstract | Acrolein (C(3)H(4)O) and 1-butene (C(4)H(8)) can both be individually detected by proton transfer chemical ionization mass spectrometry (CI-MS). However, because these compounds are isobaric, mixtures of these two compounds cannot be resolved since both compounds react with H(3)O(+) via a proton-transfer reaction to form a protonated molecule that is detected at a nominal mass-to-charge ratio of 57 (m/z 57). While both compounds react with H(3)O(+) only acrolein reacts to any significant extent with H(3)O(+)(H(2)O). Recognizing that the electrical potential applied to a drift tube reaction mass spectrometer provides a simple and effective means for varying the relative intensity of the H(3)O(+) and H(3)O(+)(H(2)O) reactant ions we have developed a method whereby we make use of this reactivity difference to resolve mixtures of these two compounds. We demonstrate a technique where the individual contributions of acrolein and 1-butene within a mixture can be quantitatively resolved by systematically changing the reagent ion from H(3)O(+) to H(3)O(+)(H(2)O) through control of the electric potential applied to the drift tube reaction region of a proton transfer reaction mass spectrometer. Copyright (c) 2008 John Wiley & Sons, Ltd. | | Language | ENG | | Pub Type(s) | JOURNAL ARTICLE
| | PubMed ID | 18649292 |
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