Analysis of carbonyl compounds via headspace solid-phase microextraction with on-fiber derivatization and gas chromatographic–ion trap tandem mass spectrometric determination of their O-(2,3,4,5,6-pentafluorobenzyl)oxime derivatives

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• 作者：Hans-Georg Schmarr ; Theodoros Potouridis ; Sebastian Ganß ; Wei Sang ; Benedikt Kö ; pp ; Ursula Bokuz ; Ulrich Fischer
• 关键词：Carbonyls ; Aldehydes ; O-(2 ; 3 ; 4 ; 5 ; 6-Pentafluorobenzyl)hydroxylamine hydrochloride ; Oximes ; HS-SPME-GC-MS-MS ; Ion trap mass spectrometry ; Retention indices ; Electron ionization mass spectra
• 刊名：Analytica Chimica Acta
• 出版年：2008
• 期刊代码：2_00032670
• 类别：ch
• 出版时间：9 June 2008
• 卷：617
• 期：1-2
• 页码：119-131
• 文件大小：677 K

摘要

An improved method for the analysis of carbonyls is described utilizing a headspace solid-phase microextraction (HS-SPME) step and on-fiber derivatization with O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine (PFBHA) hydrochloride. Thermal desorption of the oxime derivatives formed on the fiber is followed by gas chromatographic separation coupled to an ion trap tandem mass spectrometer (GC–ITMS). Selecting specific fragment ions within the electron ionization (EI⁺) mass spectra of these oxime derivatives as precursor ions for MS–MS fragmentation provides a suitable method for the target analysis of individual carbonyl classes, such as alkanals, (E)-2-alkenals, (E,E)-2,4-alkadienals, and others. Retention indices on polar as well as on apolar stationary phases along with EI⁺ mass spectra patterns are presented for a large set of oxime derivatives, giving valuable information needed for unambiguous assignment of substances in complex sample matrices. The fast sample preparation and derivatization step via HS-SPME can be automated and is applicable to a variety of biological samples and foodstuffs, allowing rapid and sensitive screening analyses of important aldehydic biomarkers and aroma active compounds.