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The reactions of H3O+, NO+ and O2+ with several flavourant esters studied using selected ion flow tube mass spectrometry
被引:17
|作者:
Iachetta, Liana
[2
]
Malek, Lada
[2
]
Ross, Brian M.
[1
,2
,3
]
机构:
[1] Lakehead Univ, Div Med Sci, No Ontario Sch Med, Thunder Bay, ON P7B 5E1, Canada
[2] Lakehead Univ, Dept Biol, Thunder Bay, ON P7B 5E1, Canada
[3] Lakehead Univ, Dept Chem, Thunder Bay, ON P7B 5E1, Canada
关键词:
VOLATILE COMPOUNDS;
ROYAL-GALA;
SIFT-MS;
FLAVOR;
GAS;
QUANTIFICATION;
DISCRIMINATION;
HEADSPACE;
BREATH;
MODELS;
D O I:
10.1002/rcm.4439
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
The reactions of H3O+, NO+, and O-2(+) with nineteen ester compounds occurring naturally in plants, and having important flavourant properties, were examined using selected ion flow tube mass spectrometry (SIFT-MS). The H3O+ reactions primarily generate [R1COOR2 center dot H](+), and may also produce [R-2](+) fragment ions and/or fragmentation within the ester linkage. Collisional association/adduct ions, [R1COOR2 center dot NO](+), are the main products formed in the NO reactions, although the carboxyl fragment ion is also detected frequently. The identification of the parent compound may be made more easily in the H3O+ and NO+ reactions. The inclusion of O-2(+) reactions in the analysis provides additional information, which may be applied when the identity of a parent compound cannot be determined solely from the H3O+ and NO+ analysis. Consideration of the product ions generated with the three precursors suggests that SIFT-MS can differentiate between many of the esters investigated, including isomers, although the product ions generated in the reactions with some esters are too similar to allow independent quantification. Our data therefore suggest that SIFT-MS may be a useful tool to rapidly analyse and quantify flavourant esters in complex gas mixtures. Copyright (C) 2010 John Wiley & Sons, Ltd.
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页码:815 / 822
页数:8
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