Schorr Pascal, Volmer Dietrich A
Bioanalytical Chemistry, Humboldt-Universität zu Berlin, Brook-Taylor-Str. 2, 12489, Berlin, Germany.
Anal Bioanal Chem. 2019 Sep;411(24):6247-6253. doi: 10.1007/s00216-019-01789-z. Epub 2019 Apr 10.
Gas phase ion/molecule reactions are often used in analytical applications to support the analysis of isomers or to identify specific functional groups of organic molecules. Until now, deliberate chemical reactions have not been performed in differential ion mobility spectrometry (DMS) devices except for hydrogen exchange and cluster formation. The present work extends that of Colorado and Brodbelt (Anal Chem 66:2330-5, 1994) on ion/molecule reactions in an ion trap mass spectrometer. In this study, class-specific chemical reactions of 4-quinolone antibiotics with various chemical reagents were used to demonstrate the analytical utility of ion/molecule reactions in a DMS drift cell. For these reactions, dehydrated reactive precursor ions were initially formed and made to undergo annulation reactions with selected reagents within the timescale of the DMS separation. Careful study of the energies required for dissociation of the adducts confirmed the covalent nature of the newly formed bond; thus demonstrating the analytical utility of this approach. Graphical abstract.
气相离子/分子反应常用于分析应用中,以辅助异构体分析或识别有机分子的特定官能团。到目前为止,除了氢交换和簇形成外,尚未在差分离子迁移谱(DMS)设备中进行过有意的化学反应。目前的工作扩展了科罗拉多大学和布罗德贝尔特(《分析化学》66:2330 - 2335,1994年)在离子阱质谱仪中关于离子/分子反应的研究。在本研究中,使用4 - 喹诺酮类抗生素与各种化学试剂的类别特异性化学反应,来证明离子/分子反应在DMS漂移管中的分析效用。对于这些反应,最初形成脱水的反应性前体离子,并使其在DMS分离的时间尺度内与选定的试剂发生环化反应。对加合物解离所需能量的仔细研究证实了新形成键的共价性质;从而证明了该方法的分析效用。图形摘要。