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等离子体-纳米液滴反应条件下的电荷反转排除了不饱和脂肪酸的费歇尔酯化反应:一种用于II型等压重叠的化学方法。

Charge inversion under plasma-nanodroplet reaction conditions excludes Fischer esterification for unsaturated fatty acids: a chemical approach for type II isobaric overlap.

作者信息

Kulyk Dmytro S, Baryshnikov Glib V, Damale Purva S, Maher Simon, Badu-Tawiah Abraham K

机构信息

Department of Chemistry and Biochemistry, The Ohio State University 100 West 18th Ave. Columbus OH 43210 USA

Laboratory of Organic Electronics, Department of Science and Technology, Linköping University SE-60174 Norrköping Sweden.

出版信息

Chem Sci. 2023 Dec 12;15(3):914-922. doi: 10.1039/d3sc05369e. eCollection 2024 Jan 17.

Abstract

Direct infusion ionization methods provide the highest throughput strategy for mass spectrometry (MS) analysis of low-volume samples. But the trade-off includes matrix effects, which can significantly reduce analytical performance. Herein, we present a novel chemical approach to tackle a special type of matrix effect, namely type II isobaric overlap. We focus on detailed investigation of a nanodroplet-based esterification chemistry for differentiating isotopologue [M + 2] signal due to unsaturated fatty acid (FA) from the monoisotopic signal from a saturated FA. The method developed involves the online fusion of nonthermal plasma with charged nanodroplets, enabling selective esterification of saturated FAs. We discovered that unsaturated FAs undergo spontaneous intramolecular reaction a novel mechanism based on a carbocation intermediate to afford a protonated lactone moiety (resonance stabilized cyclic carbonium ion), whose mass is the same as the original protonated unsaturated FA. Therefore, the monoisotopic signal from any saturated FA can be selectively shifted away from the mass-to-charge position where the isobaric interference occurs to enable effective characterization by MS. The mechanism governing the spontaneous intramolecular reactions for unsaturated FAs was validated with DFT calculations, experimentation with standards, and isotope labeling. This novel insight achieved the ultrafast plasma-nanodroplet reaction environment provides a potentially useful synthetic pathway to achieve catalyst-free lactone preparation. Analytically, we believe the performance of direct infusion MS can be greatly enhanced by combining our approach with prior sample enrichment steps for applications in biomedicine and food safety. Also, combination with portable mass spectrometers can improve the efficiency of field studies since front-end separation is not possible under such conditions.

摘要

直接注入电离方法为低体积样品的质谱(MS)分析提供了最高通量的策略。但权衡之处在于基质效应,它会显著降低分析性能。在此,我们提出一种新颖的化学方法来解决一种特殊类型的基质效应,即II型等压重叠。我们专注于详细研究基于纳米滴的酯化化学,以区分不饱和脂肪酸(FA)产生的同位素异构体[M + 2]信号与饱和FA的单同位素信号。所开发的方法涉及非热等离子体与带电纳米滴的在线融合,从而实现饱和FA的选择性酯化。我们发现不饱和FA会发生自发的分子内反应——一种基于碳正离子中间体的新机制,生成质子化的内酯部分(共振稳定的环状碳鎓离子),其质量与原始质子化不饱和FA相同。因此,任何饱和FA的单同位素信号都可以选择性地从等压干扰发生的质荷位置偏移开,以便通过MS进行有效表征。通过密度泛函理论计算、标准品实验和同位素标记验证了不饱和FA自发分子内反应的机制。这一新颖的见解实现了——超快的等离子体 - 纳米滴反应环境为实现无催化剂内酯制备提供了一条潜在有用的合成途径。在分析方面,我们认为将我们的方法与先前的样品富集步骤相结合,可大大提高直接注入MS在生物医学和食品安全应用中的性能。此外,与便携式质谱仪结合可以提高现场研究的效率,因为在这种情况下无法进行前端分离。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/967e/10793210/3c9a04a57f5b/d3sc05369e-s1.jpg

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