Investigation on the preparation and chromatographic behavior of a new para-tert-butylcalix[4]arene-1,2-crown-4 stationary phase for high performance liquid chromatography

• Published in: Talanta (Oxford) 2011-07, Vol.85 (1), p.317-324
• Main Authors: Hu, Kai, Zhao, Wenjie, Wen, Fuyong, Liu, Junwei, Zhao, Xiaolan, Xu, Zhanhui, Niu, Bailin, Ye, Baoxian, Wu, Yangjie, Zhang, Shusheng
• Format: Article
• Language: English
• Subjects: Analytical chemistry; Aromatic amines; Benzoic acid; Calixarenes; Calixarenes - chemical synthesis; Calixarenes - chemistry; Chemistry; Chromatographic methods and physical methods associated with chromatography; Chromatography; Chromatography, High Pressure Liquid - methods; Crown Ethers - chemical synthesis; Crown Ethers - chemistry; Exact sciences and technology; Hydrogen Bonding; Hydrophobic and Hydrophilic Interactions; Inclusions; Indicators and Reagents; Methyl alcohol; Other chromatographic methods; Para-tert-Butylcalixarene stationary phase; Polycyclic aromatic hydrocarbons; Quantum chemistry; Quantum chemistry calculation; Selectivity; Separation mechanism; Thermodynamics
• ISSN: 0039-9140; 1873-3573
• DOI: 10.1016/j.talanta.2011.03.068

In the present work, a new para-tert-butylcalix[4]arene-1,2-crown-4 bonded silica stationary phase (CBS4-4) was synthesized, structurally characterized, and employed to separate polycyclic aromatic hydrocarbons (PAHs), phenols, aromatic amines, benzoic acid and its derivatives. The chromatographic behaviors of the prepared stationary phase were investigated and compared with ODS. The effects of methanol concentrations on the retention index show that CBS4-4 exhibits high selectivity for the above analytes. The separation mechanisms based on the different interactions between calixarene and the analytes were discussed. With the assistance of quantum chemistry calculation, the interaction Gibbs free energy change ΔGsolv (in the mobile phase) of p, m and o-phenylenediamine positional isomers and para-tert-butylcalix[4]arene-1,2-crown-4 were obtained. The ΔGsolv values were consistent with the retention behavior of p, m and o-phenylenediamine on the CBS4-4. According to the chromatographic data, it can be concluded that the selectivity of CBS4-4 for analytes is mainly ascribed to hydrophobic interaction, accompanied by other effects such as hydrogen bonding interaction, π–π and inclusion interaction. The CBS4-4 column has been successfully employed for the analysis of benzoic acid in Sprite drink.