Cross‐linked polysiloxane‐coated stable bond O‐9‐(2,6‐diisopropylphenylcarbamoyl)quinine and quinidine chiral stationary phases as well as application in enantioselective cryo‐HPLC

Abstract

AbstractIn this work, brush‐type chiral stationary phases (CSPs) with O‐9‐(2,6‐diisopropylphenylcarbamoyl)‐modified quinidine (DIPPCQD‐brush/‐SH) and O‐9‐(2,6‐diisopropylphenylcarbamoyl)‐modified quinine (DIPPCQN‐brush/‐SH) were prepared as benchmarks for comparison with new corresponding polymeric CSPs with more stable bonding chemistry. These polymeric CSPs were prepared by coating a thin poly(3‐mercaptopropyl)‐methylsiloxane film together with the chiral selector onto vinyl‐modified silica. In a second step, immobilization of the quinine/quinidine derivatives as well as cross‐linking of the polysiloxane film to the vinyl‐silica is achieved by a double thiol‐ene click reaction. The polymeric CSPs exhibited similar enantioselectivity as the corresponding brush phases, but showed lower chromatographic efficiencies. Chiral acidic substances were separated into enantiomers (e.g., N‐protected amino acids, herbicides like dichlorprop) in accordance with an enantioselective anion‐exchange process. Oxidation of residual thiol groups of the polymer DIPPCQN‐CSP introduced sulfonic acid co‐ligands on the silica surface, which resulted in greatly reduced retention times. Acting as immobilized counterions, they allowed to reduce the concentration of counterions in the mobile phase, which is favorable for liquid chromatography (LC)–electrospray ionization–mass spectrometry application. Ibuprofen showed a single peak under ambient column temperature. However, application of cryogenic cooling of the column enabled to achieve baseline separation at –20°C column temperature. It can be explained by an enthalpically dominated separation, which leads to an increase in separation factors when the temperature is reduced. While it is quite uncommon to work at subzero degree column temperature, this work illustrates the potential to exploit such temperature regime for optimization of LC enantiomer separations.