Abstract
We synthesized seven different polymethacrylate monolithic capillary columns using N,N-dimethyl-N-metacryloxyethyl-N-(3-sulfopropyl) ammonium betaine functional monomer (MEDSA) and various cross-linking monomers differing in the polarity and size. The efficiency of monolithic columns for polar low-molecular compounds in the aqueous normal-phase (HILIC) mode depends rather on the polarity, than on the size of the cross-linker molecules. Cross-linking molecules, which exhibit high polarity can produce poly(methacrylate) monoliths with an increase in pore sizes below 50nm. Columns prepared with pentaerythritol triacrylate or bisphenol A dimethacrylate cross-linkers show large inner pore (mesopore) porosity, and provide poor efficiency, whereas columns with trioxyethylene dimethacrylate (TriEDMA) and tetraoxyethylene dimethacrylate (TeEDMA) cross-linkers showed poor permeability. Columns prepared using dioxyethylene dimethacrylate (DiEDMA), and especially glycerolate dimethacrylate (BIGDMA) cross-linkers, showed best efficiency, with more 60,000–70,000 theoretical plates/m, almost twice in comparison to (poly)methylene dimethacrylate (HEDMA) in the HILIC mode. All columns show dual retention mechanism and can be used for separations of low-molcular compounds such as phenolic acids in the HILIC mode in acetonitrile-rich mobile phases and in the reversed-phase mode in mobile phases with higher concentrations of water. Some columns show broad pore distribution and can be used for size-exclusion chromatography of non-polar polymers in tetrahydrofuran.
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