Researchers from the Shanghai Institute of Organic Chemistry of the Chinese Academy of Sciences recently developed a new platform for rapid chiral analysis, producing chromatogram-like output without the need for separation. The study was published in Cell Reports Physical Science.
Molecules not superimposable on their mirror images are chiral and play essential roles in the pharmaceutical industry, material sciences, and the origin of life. Distinguishing between mirror-image molecules is in great demand, but existing approaches usually achieve this goal with compromise in accuracy or efficiency.
Specifically, chromatographic methods resolve chiral molecules through easily interpretable chromatogram peaks, but require time-consuming separation. Chiroptical responsive systems allow in-situ chiral analysis, but are often plagued by sample interference issues.
In this study, the researchers developed a series of 19F-labeled chiral aluminum complexes that reversibly bind to various Lewis basic analytes.
The inclusion of chiral analytes to the confined binding pocket produced chromatogram-like 19F NMR signals, allowing rapid and unambiguous chiral analysis.
The method is operationally simple and effectively resolved a wide range of chiral molecules, including alcohols, ethers, amides, carbamates, oxazolidinones, sulfoxides, and sulfoximines.
The study shows that simultaneous analysis of three different classes of chiral compounds can be achieved in the absence of separation.
According to the researchers, the new method may also be used to determine the enantiopurity of crude reaction products and the assignment of absolute configurations. When used in conjunction with an autosampling NMR spectrometer, greater than 1,000 chiral analyses can be performed in a day.
"Such a method has the potential to simultaneously identify multiple analytes and existing interferences, which may eventually lead to real-time chiral analysis in complex biologically relevant systems," said ZHAO Yanchun, corresponding author of the study.
Separation-free Enantiodifferentiation with Chromatogram-like Output. Yipeng Li et al. Cell Reports Physical Science, 1 July 2020, 100100, https://doi.org/10.1016/j.xcrp.2020.100100.
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