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采用选择离子流管质谱法分析酮类物质。

Analysis of ketones by selected ion flow tube mass spectrometry.

作者信息

Smith David, Wang Tianshu, Spanĕl Patrik

机构信息

Centre for Science and Technology in Medicine, School of Medicine, Keele University, Thornburrow Drive, Hartshill, Stoke-on-Trent ST4 7QB, UK.

出版信息

Rapid Commun Mass Spectrom. 2003;17(23):2655-60. doi: 10.1002/rcm.1244.

Abstract

A selected ion flow tube mass spectrometry (SIFT-MS) study of the reactions of H3O+, NO+ and O2+* ions with the ketones (M) 2-heptanone, 2-octanone, 2-nonanone, 2-undecanone and 2-aminoacetophenone has been conducted in preparation for studies of volatile emissions from bacteria. The H3O+ reactions all proceed rapidly via exothermic proton transfer, producing only MH+ ions that form their monohydrates when water vapour is present in the helium carrier gas. The O2+* reactions proceed rapidly via dissociative charge transfer producing parent cations M+* and some fragment ions. The NO+ reactions form the NO+M adduct ions at rates which are dependent on the pressure of the helium carrier gas. Combining the present NO+ kinetic data with those available from previous SIFT studies, the phenomenon of charge transfer complexing is clearly demonstrated. This results in adduct formation in these NO+/ketone reactions at or near the collisional rate. SIFT-MS spectra are presented to illustrate the simplicity of SIFT-MS analysis of ketones using both H3O+ and NO+ precursor ions.

摘要

为了开展对细菌挥发性排放物的研究,已经进行了一项选择离子流管质谱法(SIFT-MS)研究,研究对象是H3O+、NO+和O2+*离子与酮类物质(M)(2-庚酮、2-辛酮、2-壬酮、2-十一烷酮和2-氨基苯乙酮)之间的反应。H3O+反应均通过放热质子转移迅速发生,仅产生MH+离子,当氦载气中存在水蒸气时,这些离子会形成它们的一水合物。O2+*反应通过离解电荷转移迅速进行,产生母体阳离子M+*和一些碎片离子。NO+反应以取决于氦载气压力的速率形成NO+M加合离子。将当前的NO+动力学数据与先前SIFT研究中可得的数据相结合,电荷转移络合现象得到了清晰的证明。这导致在这些NO+/酮反应中以碰撞速率或接近碰撞速率形成加合物。给出了SIFT-MS光谱,以说明使用H3O+和NO+前体离子对酮进行SIFT-MS分析的简便性。

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