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Real-time monitoring of chemical transformations by ultrafast 2D NMR spectroscopy

机译:通过超快2D NMR光谱实时监测化学转化

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An approach enabling the acquisition of 2D nuclear magnetic resonance (NMR) spectra within a single scan has been recently proposed. A promising application opened up by this "ultrafast" data acquisition format concerns the monitoring of chemical transformations as they happen, in real time. The present paper illustrates some of this potential with two examples: (i) following an H/D exchange process that occurs upon dissolving a protonated protein in D2O, and (ii) real-time in situ tracking of a transient Meisenheimer complex that forms upon rapidly mixing two organic reactants inside the NMR observation tube. The first of these measurements involved acquiring a train of 2D H-1-N-15 HSQC NMR spectra separated by ca. 4 s; following an initial dead time, this allowed us to monitor the kinetics of hydrogen exchange in ubiquitin at a site-resolved level. The second approach enabled us to observe, within ca. 2 s after the triggering of the reaction, a competition between thermodynamic and kinetic controls via changes in a series of 2D TOCSY patterns. The real-time dynamic experiments hereby introduced thus add to an increasing family of fast characterization techniques based on 2D NMR; their potential and limitations are briefly discussed.
机译:最近已经提出了一种能够在单次扫描内采集2D核磁共振(NMR)光谱的方法。这种“超快速”的数据采集格式开辟的有前途的应用涉及实时监测化学转化的发生。本文通过两个例子说明了这种潜力中的一些:(i)在将质子化的蛋白质溶解在D2O中后发生的H / D交换过程,以及(ii)实时原位追踪形成于在NMR观察管内快速混合两种有机反应物。这些测量中的第一个涉及获取由2d分开的2D H-1-N-15 HSQC NMR谱图。 4秒在初始死区时间之后,这使我们能够以位点分辨的水平监测遍在蛋白中氢交换的动力学。第二种方法使我们能够在大约触发反应后2秒钟,通过一系列2D TOCSY模式的变化,热力学和动力学控制之间发生竞争。因此,本文介绍的实时动态实验增加了基于2D NMR的快速表征技术家族;简要讨论了它们的潜力和局限性。

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