2008
DOI: 10.1016/j.chroma.2007.11.023
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Characteristic fragmentation patterns of the trimethylsilyl and trimethylsilyl–oxime derivatives of various saccharides as obtained by gas chromatography coupled to ion-trap mass spectrometry

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Cited by 42 publications
(25 citation statements)
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“…In the analysis of free metabolites, the fragment m/z 361 of the Suc trimethylsilyl derivative was monitored. This abundant ion results from fragmentation at the glycosidic linkage, leading to m/z 361 (C 15 H 33 O 4 Si 3 ) representing all six carbons of the glucosyl moiety of the Suc molecule (Fuzfai et al, 2008). Mass spectral data were extracted using the ChemStation Program (MSD ChemStation; Agilent Technologies).…”
Section: Gc-ms Analysis Of Labeling Profilesmentioning
confidence: 99%
“…In the analysis of free metabolites, the fragment m/z 361 of the Suc trimethylsilyl derivative was monitored. This abundant ion results from fragmentation at the glycosidic linkage, leading to m/z 361 (C 15 H 33 O 4 Si 3 ) representing all six carbons of the glucosyl moiety of the Suc molecule (Fuzfai et al, 2008). Mass spectral data were extracted using the ChemStation Program (MSD ChemStation; Agilent Technologies).…”
Section: Gc-ms Analysis Of Labeling Profilesmentioning
confidence: 99%
“…GC-MS is the most widely applied technique for the characterization of organic aerosols since it yields excellent results in terms of separation, sensitivity and number of species analyzed in the identification and quantification of many compounds [1,[3][4][5]10,12,13,17,19,[23][24][25][26][27][28][29][30][31]. Indeed, multi-residue analytical methodologies, that achieve simultaneous analysis of several compounds, are useful for reducing the complexity and time required for sample preparation and analysis in order to provide a large amount of reliable data on molecular tracers in atmospheric PM samples [1,[3][4][5]12].…”
Section: Introductionmentioning
confidence: 99%
“…The data for the representative target analytes are reported in bold XLOD (5th column) computed as XLOD = 6 b /b1, where b1 is the slope of the calibration line, XLOD*, (6th column) computed as the concentration corresponding to three times the standard deviation of the peak areas generated by blank filters. (N,O-bis(trimethylsilyl)-trifluoroacetamide) as silylation reagent has been widely used to analyze polyacids and sugars/sugar alcohols in PM samples, since it provides the low detection limits (≤2 ng m −3 ) and high reproducibility required by environmental monitoring [1,3,4,12,18,23,[25][26][27][28][29][30][31]. The silylation conditions reported by various authors widely differ, and at times are even contradictory, because these procedures usually focus on analysis of a particular class of compounds, i.e., carboxylic acids or sugars [1][2][3][4][15][16][17][18][19]23,24].…”
Section: Introductionmentioning
confidence: 99%
“…Given that our intention was not to identify individual simple sugar components, the analysis is further done by selecting specific abundant fragment ions of simple sugars. By selecting ions 204 and 217m/z, characteristics of TMS derivatives of monosaccharides (pyranose and furanose ring, respectively) (Karady and Pines 1970;Ačanski and Vujić 2014), and 361m/z, characteristic abundant fragment ion of TMS derivatives of di-and trisaccharides (Füzfai et al 2008), the selected ion monitoring (SIM) chromatograms were obtained from complex TIC chromatograms, which simplified the detection procedure of simple sugar derivative peaks in the chromatograms.…”
Section: Resultsmentioning
confidence: 99%