Silica modification with 9-methylacridine and 9-undecylacridine as mixed-mode stationary phases in HPLC.

In this research, 9-methylacridine and 9-undecylacridine were synthesized through Bernthsen's reaction and well characterized using gas chromatography-mass spectrometry (GC-MS) and nuclear magnetic resonance (NMR). Two mixed-mode stationary phases were developed by functionalizing silica with 9-methylacridine and 9-undecylacridine. Then, two modified silicas were characterized by elemental analysis, thermogravimetric analysis (TGA), and fourier transform-infrared spectroscopy (FT-IR). Due to the extent of conjugative rings, the hydrophobic hydrocarbon chain, and anion exchange sites of 9-methylacridinium and 9-undecylacridinium group on the silica gel of columns, mixed-mode stationary phases were designed with multiple interactions including π-π stacking interaction, reverse phase, hydrophilic interaction, and anion exchange. According to the type of acridine, different interactions may be formed in the target column. Polycyclic aromatic hydrocarbons (PAHs), alkylbenzenes, pyridines and parabens were chromatographed on π-π stacking modes and RPLC, where anion exchange sites can be applied for the separation of inorganic anions on AEC mode. Considering the structure of the stationary phases, these columns were used to separate organic compounds with higher polarity on the HILIC retention. The performance of the columns was investigated by the chromatographic parameters in terms of column efficiency (N/m), asymmetry factor (A), retention factor (k), and resolution (Rs). The mixed-mode stationary phases can be successfully employed to conduct chromatographic separation on a wide range of samples with a single column.