Differentiating Isomeric Urea Derivatives by Cyclic Ion Mobility-Mass Spectrometry, Host-Guest Chemistry, and Tandem Mass Spectrometry.

IF 3.1 2区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Sudam S Mane, Cole D Warner, David V Dearden, Kenneth W Lee
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引用次数: 0

Abstract

Alkyl pyridyl ureas are crucial precursors in medicinal and agricultural chemistry. Their isomeric forms, which are distinguished by the position of pyridyl nitrogen relative to the urea functionality, pose challenges in mass spectrometric identification due to their isobaric molecular ions. This study presents orthogonal methods to differentiate 1-phenyl-3-(2-pyridyl) urea (ortho), 1-phenyl-3-(3-pyridyl) urea (meta), and 1-phenyl-3-(4-pyridyl) urea (para). Cyclic ion mobility separation of protonated molecules and their complexes with β-cyclodextrin was employed. While the protonated ortho and para isomers were baseline resolved after six passes, the meta and para isomers were not separated after 40 passes. After complexation with β-cyclodextrin, we observed two peaks for each isomer. The peak that arrived first (peak A) is a doubly protonated dimer of the host-guest complex, while the later arriving peak (peak B) corresponds to the singly protonated host-guest complex. Peak B for the β-cyclodextrin complex of the meta and para compounds was resolved after three passes. Thus, the differentiation of meta and para isomers was achieved after complexation with β-cyclodextrin. Overall, the two methods (ion mobility of protonated molecules and ion mobility of host-guest complexes) led to orthogonal results. Collision-induced dissociation of protonated molecules revealed identical fragment ions at m/z 95 and 121, but their relative intensities varied among isomers, enabling their clear differentiation. Additionally, collision-induced dissociation of host-guest complexes at 20 eV shows that the meta isomer forms the most stable complex with β-cyclodextrin and the para isomer forms the least stable complex, which provides additional orthogonal information to differentiate the three isomers. These findings provide a basis for cyclic traveling wave ion mobility and tandem mass spectrometry-based identification and characterization of other isomeric phenyl pyridyl ureas.

用循环离子迁移-质谱法、主-客体化学和串联质谱法鉴别同分异构体尿素衍生物。
烷基吡啶脲是医药和农业化学的重要前体。它们的异构体形式是由吡啶基氮相对于尿素官能团的位置来区分的,由于它们的分子离子等压,在质谱鉴定中提出了挑战。本研究采用正交法对1-苯基-3-(2-吡啶基)尿素(邻位)、1-苯基-3-(3-吡啶基)尿素(间位)和1-苯基-3-(4-吡啶基)尿素(对位)进行了区分。采用环离子迁移率分离质子化分子及其与β-环糊精配合物。虽然质子化的邻位异构体和对异构体在6次后被基线分离,但在40次后未分离间位异构体和对异构体。在与β-环糊精络合后,我们观察到每个异构体有两个峰。最先到达的峰(峰A)是主-客复合物的双质子二聚体,而较晚到达的峰(峰B)对应于单质子的主-客复合物。中间和对位化合物的β-环糊精配合物的B峰在三次通过后被分解。因此,与β-环糊精络合后实现了间位异构体和对位异构体的分化。总的来说,两种方法(质子化分子的离子迁移率和主客体配合物的离子迁移率)的结果是正交的。质子化分子的碰撞诱导解离在m/z 95和121处显示出相同的片段离子,但它们的相对强度在不同的异构体中不同,使它们能够明显区分。此外,在20 eV的碰撞诱导下,主客体配合物的解离表明,中间异构体与β-环糊精形成最稳定的配合物,而对异构体形成最不稳定的配合物,这为区分三种异构体提供了额外的正交信息。这些发现为基于循环行波离子迁移率和串联质谱的其他异构体苯基吡啶脲的鉴定和表征提供了基础。
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来源期刊
CiteScore
5.50
自引率
9.40%
发文量
257
审稿时长
1 months
期刊介绍: The Journal of the American Society for Mass Spectrometry presents research papers covering all aspects of mass spectrometry, incorporating coverage of fields of scientific inquiry in which mass spectrometry can play a role. Comprehensive in scope, the journal publishes papers on both fundamentals and applications of mass spectrometry. Fundamental subjects include instrumentation principles, design, and demonstration, structures and chemical properties of gas-phase ions, studies of thermodynamic properties, ion spectroscopy, chemical kinetics, mechanisms of ionization, theories of ion fragmentation, cluster ions, and potential energy surfaces. In addition to full papers, the journal offers Communications, Application Notes, and Accounts and Perspectives
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