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Probing Electrospray Ionization Dynamics Using Differential Mobility Spectrometry: The Curious Case of 4-Aminobenzoic Acid

机译:使用差动迁移谱法探测电喷雾电离动力学:4-氨基苯甲酸的奇怪案例

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Here, we present the separation of two ions that differ only by the site of protonation of the analyte molecule using differential mobility spectrometry (DMS). Protonated 4-aminobenzoic acid molecules (4-ABA) generated by positive-mode electrospray ionization [ESI(+)] can exist with the proton residing on either the amine nitrogen (N-protonated) or the carboxylic acid oxygen (O-protonated), and the protonation site can differ on the basis of the solvent system used. In this study, we demonstrate the identification and separation of N- and O-protonated 4-ABA using DMS, with structural assignments verified by: (1) the presence of distinct peaks in the DMS ionogram, (2) the observed effects resulting from altering the ESI(+) solvent system, (3) the observed ~(13)C NMR chemical shifts arising from altering the solvent system, (4) the observation of distinct MS/MS fragmentation patterns for the two DMS-separated ions, (5) the unique hydrogen-deuterium exchange behavior for these ions, and (6) the fundamental behavior of these two ions within the DMS cell, linked back to the structural differences between the two protonated forms.
机译:在这里,我们介绍了使用差分迁移谱(DMS)分离仅因分析物分子的质子化位置而不同的两个离子的分离方法。通过正模式电喷雾电离[ESI(+)]生成的质子化的4-氨基苯甲酸分子(4-ABA)可以与质子位于胺氮(N质子化)或羧酸氧(O质子化)上一起存在,并且质子化位置可能会因所使用的溶剂系统而异。在这项研究中,我们证明了使用DMS鉴定和分离N-和O-质子化的4-ABA,并通过以下方法验证了结构分配:(1)DMS离子图中存在明显的峰,(2)观察到的由改变ESI(+)溶剂系统,(3)观察到由于改变溶剂系统而产生的〜(13)C NMR化学位移,(4)观察到两个DMS分离的离子的独特MS / MS碎片图谱,( 5)这些离子独特的氢-氘交换行为,以及(6)DMS电池内这两个离子的基本行为,与两种质子化形式之间的结构差异有关。

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