2019
DOI: 10.1134/s1061934819060078
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Separation of 2-Bromobutane, 2-Chlorobutane, 2-Chloropentane, and 2-Butanol Enantiomers Using a Stationary Phase Based on a Supramolecular Uracil Structure

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Cited by 5 publications
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“…This layer can be used for the separation of 2-butanol, 2-bromobutane, and other substances by GC, in which the cyclization selectivity is the result of the removal of the central molecule of the supramolecular structure at 200 °C. Similarly, in 2019, Nafikova et al [ 75 ] investigated a uracil structure as a stationary phase and successfully separated the enantiomers of several substances. In the temperature range studied, the enantiomers of 2-bromobutane and 2-chlorobutane were completely separated at 45 °C in 210 and 180 s, and the enantiomers of 2-chlorobutane were separated at 60 °C in 160 s. Guskov et al [ 74 ] used indirect methods of static adsorption with polarization control and GC to differentially adsorb enantiomers on modified adsorbents, demonstrating the usefulness of chiral recognition scaffolds ( Figure 4 c).…”
Section: Chromatographic Separationmentioning
confidence: 99%
“…This layer can be used for the separation of 2-butanol, 2-bromobutane, and other substances by GC, in which the cyclization selectivity is the result of the removal of the central molecule of the supramolecular structure at 200 °C. Similarly, in 2019, Nafikova et al [ 75 ] investigated a uracil structure as a stationary phase and successfully separated the enantiomers of several substances. In the temperature range studied, the enantiomers of 2-bromobutane and 2-chlorobutane were completely separated at 45 °C in 210 and 180 s, and the enantiomers of 2-chlorobutane were separated at 60 °C in 160 s. Guskov et al [ 74 ] used indirect methods of static adsorption with polarization control and GC to differentially adsorb enantiomers on modified adsorbents, demonstrating the usefulness of chiral recognition scaffolds ( Figure 4 c).…”
Section: Chromatographic Separationmentioning
confidence: 99%