Abstract

Semiochemicals are often produced in infinitesimally small quantities, so their isolation requires large amounts of starting material, not only requiring significant effort in sample preparation, but also resulting in a complex mixture of compounds from which the bioactive compound needs to be purified and identified. Often, compounds cannot be unambiguously identified by their mass spectra alone, and NMR analysis is required for absolute chemical identification, further exacerbating the situation because NMR is relatively insensitive and requires large amounts of pure analyte, generally more than several micrograms. We developed an integrated approach for purification and NMR analysis of <1 µg of material. Collections from high performance preparative gas-chromatography are directly eluted with minimal NMR solvent into capillary NMR tubes. With this technique, 1H-NMR spectra were obtained on 50 ng of geranyl acetate, which served as a model compound, and reasonable H-H COSY NMR spectra were obtained from 250 ng of geranyl acetate. This simple off-line integration of preparative GC and NMR will facilitate the purification and chemical identification of novel volatile compounds, such as insect pheromones and other semiochemicals, which occur in minute (sub-nanogram), and often limited, quantities.

Highlights

  • NMR spectrometry is a powerful tool to identify the chemical structures of novel compounds

  • We describe here a simple off-line integration of the preparative GC technique and capillary NMR analysis to facilitate the identification of minute amounts of small volatile compounds

  • In order to specify those signals, first, fresh benzene-d6 was loaded into an NMR tube with a GC syringe, and the tube was subjected to 1H-NMR analysis as a blank sample

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Summary

Introduction

NMR spectrometry is a powerful tool to identify the chemical structures of novel compounds. The requirement for large amounts of pure material comes from the inherent relatively low sensitivity of NMR and the lack of a compound separation system in NMR analysis. This severely limits the usefulness of NMR when the source or amount of biological material is limited. To overcome these drawbacks of NMR analysis, special probes and instruments have recently been developed [1,2,3,4,5,6], and these techniques have pushed the lower boundary of NMR analysis into the microgram sample scale in some cases. In order to specify those signals, first, fresh benzene-d6 was loaded into an NMR tube with a GC syringe, and the tube was subjected to 1H-NMR analysis as a blank sample

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