首页> 外文期刊>Chemistry central journal >Induced in-source fragmentation pattern of certain novel (1Z,2E)-N-(aryl)propanehydrazonoyl chlorides by electrospray mass spectrometry (ESI-MS/MS)
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Induced in-source fragmentation pattern of certain novel (1Z,2E)-N-(aryl)propanehydrazonoyl chlorides by electrospray mass spectrometry (ESI-MS/MS)

机译:电喷雾质谱法(ESI-MS / MS)诱导某些新型(1Z,2E)-N-(芳基)丙烷肼基甲酰氯的源内裂解模式

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Background Collision induced dissociation (CID) in the triple quadrupole mass spectrometer system (QQQ) typically yields more abundant fragment ions than those produced with resonance excitation in the presence of helium gas in the ion trap mass spectrometer system (IT). Detailed product ion spectra can be obtained from one stage MS2 scan using the QQQ. In contrast, generating the same number of fragment ions in the ion trap requires multiple stages of fragmentation (MSn) using CID via in-trap resonance excitation with the associated time penalties and drop in sensitivity. Results The use of in-source fragmentation with electrospray ionization (ESI) followed by product ion scan (MS2) in a triple quadrupole mass spectrometer system, was demonstrated. This process enhances the qualitative power of tandem mass spectrometry to simulate the MS3 of ion trap for a comprehensive study of fragmentation mechanisms. A five pharmacologically significant (1Z, 2E)-N-arylpropanehydrazonoyl chlorides (3a-e) were chosen as model compounds for this study. In this work, detailed fragmentation pathways were elucidated by further dissociation of each fragment ion in the ion spectrum, essentially, by incorporating fragmentor voltage induced dissociation (in-source fragmentation) and isolation of fragments in a quadrupole cell Q1. Subsequently, CID occurs in cell, Q2, and fragment ions are analyzed in Q3 operated in product ion mode this process can be referred to as pseudo-MS3 scan mode. Conclusions This approach allowed unambiguous assignment of all fragment ions using tandem mass spectrometer and provided adequate sensitivity and selectivity. It is beneficial for structure determination of unknown trace components. The data presented in this paper provide useful information on the effect of different substituents on the ionization/fragmentation processes and can be used in the characterization of this important class of compounds.
机译:背景技术在离子阱质谱仪系统(IT)中存在氦气的情况下,三重四极杆质谱仪系统(QQQ)中的碰撞诱导解离(CID)通常产生比共振激发产生的碎片离子更丰富的碎片离子。可以使用QQQ从一级MS2扫描获得详细的产物离子光谱。相反,在离子阱中产生相同数量的碎片离子需要使用CID并通过带内共振激发的CID进行多级碎片化(MSn),并伴有时间损失和灵敏度下降。结果证明了在三重四极杆质谱系统中使用电喷雾电离(ESI)进行源内裂解,然后进行产物离子扫描(MS2)。此过程增强了串联质谱的定性能力,可以模拟离子阱的MS3,从而对碎片机理进行全面研究。选择了五种具有药理学意义的(1Z,2E)-N-芳基丙烷肼基酰氯(3a-e)作为本研究的模型化合物。在这项工作中,通过进一步离解离子谱中的每个碎片离子来阐明详细的碎裂途径,本质上是通过在四极杆电池Q1中引入碎裂器电压诱导的解离(源内碎裂)和碎片分离。随后,在单元Q2中发生CID,并在以产物离子模式运行的Q3中分析碎片离子,此过程可称为伪MS3扫描模式。结论该方法允许使用串联质谱仪明确分配所有碎片离子,并提供足够的灵敏度和选择性。这对于确定未知痕量组分的结构是有益的。本文中提供的数据提供了有关不同取代基对电离/碎片化过程影响的有用信息,可用于表征这一重要类别的化合物。

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