Issue 16, 2019

Gas chromatography–Fourier transform infrared spectroscopy reveals dynamic molecular interconversion of oximes

Abstract

This study reports gas chromatography (GC) combined with Fourier transform infrared (FTIR) spectroscopy to investigate the elution profiles of individual oxime isomers undergoing characteristic interconversion (dynamic chromatography) in GC. The use of a light-pipe FTIR interface enables on-line acquisition of FTIR spectra, which in turn render unambiguous identification of the individual molecules. Here, acetaldehyde oxime and propionaldehyde oxime were chosen for comparison of elution behaviour under varying temperature and carrier flow velocities. The choice of selective responses (wavenumber selectivity), which were relatively stronger for each isomer, enabled display and retracing of the individual isomer over the chromatographic time scale and thus provided characteristic single isomer profiles. Chemometric data analysis using the multivariate curve resolution technique further confirmed this isomer elution profile. Simulation of the spectrum for each isomer allowed comparison with instrument-generated FTIR spectra to confirm the elution order of E and Z isomers. The effect of changing chromatographic parameters (temperature, flow) on interconversion rates and/or extents were studied and the corresponding change in FTIR spectrum intensity was noted. The GC–FID data acquired concurrently with GC–FTIR analyses ratified isomerisation chromatographic profiles.

Graphical abstract: Gas chromatography–Fourier transform infrared spectroscopy reveals dynamic molecular interconversion of oximes

Supplementary files

Article information

Article type
Paper
Submitted
30 May 2019
Accepted
30 Jun 2019
First published
01 Jul 2019

Analyst, 2019,144, 4803-4812

Gas chromatography–Fourier transform infrared spectroscopy reveals dynamic molecular interconversion of oximes

J. S. Zavahir, Y. Nolvachai, B. R. Wood and P. J. Marriott, Analyst, 2019, 144, 4803 DOI: 10.1039/C9AN00990F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements