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使用台式核磁共振光谱法对化学反应进行在线监测。

On-line monitoring of chemical reactions by using bench-top nuclear magnetic resonance spectroscopy.

作者信息

Danieli E, Perlo J, Duchateau A L L, Verzijl G K M, Litvinov V M, Blümich B, Casanova F

机构信息

Institut für Technische Chemie und Makromolekulare Chemie, RWTH Aachen University, Worringerweg 1, 52074 Aachen (Germany).

出版信息

Chemphyschem. 2014 Oct 6;15(14):3060-6. doi: 10.1002/cphc.201402049. Epub 2014 Aug 8.

Abstract

Real-time nuclear magnetic resonance (NMR) spectroscopy measurements carried out with a bench-top system installed next to the reactor inside the fume hood of the chemistry laboratory are presented. To test the system for on-line monitoring, a transfer hydrogenation reaction was studied by continuously pumping the reaction mixture from the reactor to the magnet and back in a closed loop. In addition to improving the time resolution provided by standard sampling methods, the use of such a flow setup eliminates the need for sample preparation. Owing to the progress in terms of field homogeneity and sensitivity now available with compact NMR spectrometers, small molecules dissolved at concentrations on the order of 1 mmol L(-1) can be characterized in single-scan measurements with 1 Hz resolution. Owing to the reduced field strength of compact low-field systems compared to that of conventional high-field magnets, the overlap in the spectrum of different NMR signals is a typical situation. The data processing required to obtain concentrations in the presence of signal overlap are discussed in detail, methods such as plain integration and line-fitting approaches are compared, and the accuracy of each method is determined. The kinetic rates measured for different catalytic concentrations show good agreement with those obtained with gas chromatography as a reference analytical method. Finally, as the measurements are performed under continuous flow conditions, the experimental setup and the flow parameters are optimized to maximize time resolution and signal-to-noise ratio.

摘要

介绍了在化学实验室通风橱内反应器旁安装的台式系统进行的实时核磁共振(NMR)光谱测量。为了测试该系统的在线监测能力,通过在闭环中连续将反应混合物从反应器泵送到磁体并返回,研究了转移氢化反应。除了提高标准采样方法提供的时间分辨率外,这种流动设置的使用还消除了样品制备的需要。由于紧凑型NMR光谱仪目前在磁场均匀性和灵敏度方面取得的进展,浓度约为1 mmol·L⁻¹的溶解小分子可以在1 Hz分辨率的单扫描测量中进行表征。由于紧凑型低场系统的场强与传统高场磁体相比有所降低,不同NMR信号光谱的重叠是一种典型情况。详细讨论了在存在信号重叠的情况下获得浓度所需的数据处理,比较了诸如简单积分和线性拟合方法等方法,并确定了每种方法的准确性。在不同催化浓度下测得的动力学速率与作为参考分析方法的气相色谱法获得的结果显示出良好的一致性。最后,由于测量是在连续流动条件下进行的,因此对实验装置和流动参数进行了优化,以最大限度地提高时间分辨率和信噪比。

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