Key Laboratory of Synthetic and Natural Functional Molecule of Ministry of Education, Institue of Modern Separation Science, Key Lab of Modern Separation Science in Shaanxi Province, College of Chemstry & Materials Science, Northwest University, Xi'an 710127, China.
Key Laboratory of Synthetic and Natural Functional Molecule of Ministry of Education, Institue of Modern Separation Science, Key Lab of Modern Separation Science in Shaanxi Province, College of Chemstry & Materials Science, Northwest University, Xi'an 710127, China.
J Chromatogr A. 2024 Aug 2;1728:464998. doi: 10.1016/j.chroma.2024.464998. Epub 2024 May 21.
Covalent organic frameworks (COFs) show promise as a stationary phase in high performance liquid chromatography (HPLC). However, there are only a few COFs-based stationary phases developed for HPLC separation so far. Therefore, it is crucial to not only develop more varieties of COFs-type stationary phases for HPLC separation, but also to explore the retention mechanism of solutes on these stationary phases. In this paper, a new in-situ growth method was developed to prepare β-ketoenamine COF-TpPa-1@SiO composite microspheres, using spherical silica as the core material and COF-TpPa-1 fabricated by covalent conjugation of 1,3,5-triformylphloroglucinol (Tp) and p-phenylenediamine (Pa-1) as the COF shells. The resulting microspheres exhibit uniform morphology, good monodispersity, large specific surface area, narrow size distribution, and high stability. Due to diverse functional groups in the structure of COF-TpPa-1, the microspheres can offer multiple interactions, such as hydrophobic, π-π stacking and electron-donor-acceptor (EDA) between COFs and analytes. As a result, the COF-TpPa-1@SiO composite microspheres can be used as a mixed-mode stationary phase for HPLC separation. The chromatographic performance and retention mechanism of the COF-TpPa-1@SiO packed column were investigated by separating polar and non-polar solutes, as well as isomers, in various HPLC modes, including reversed-phase liquid chromatography (RPLC), hydrophilic interaction chromatography (HILIC), and RPLC/HILIC mixed-mode chromatography. The results showed successful separation of non-polar alkylbenzene homologues, polycyclic aromatic hydrocarbons (PAHs), and polar amines and phenols in RPLC mode. The "U-shaped" curves of retention factor with the ACN concentration in mobile phase for four nucleobases indicated that the solute retention on the column followed a mixed mode mechanism of RPLC/HILIC. Compared to a traditional C18 column, the COF-TpPa-1@SiO column exhibited superior separation efficiency, stability, repeatability and reproducibility in the separation of analytes with different polarities. The column enhanced the aromatic, shape and planar selectivity for PAHs and isomers through π-π interaction and improved the separation efficiency for electron-deficient compounds due to EDA effect. At last, the column was successfully used to separate and detect the residues of 5 phenylurea herbicides (PUHs) in soil. All these results indicate the potential of COFs for chromatography applications.
共价有机骨架(COFs)作为高效液相色谱(HPLC)中的固定相具有很大的发展潜力。然而,到目前为止,开发的 COFs 基固定相用于 HPLC 分离的种类还很少。因此,不仅要开发更多种类的 COFs 型固定相用于 HPLC 分离,而且要探索溶质在这些固定相上的保留机制。本文采用原位生长法,以球形二氧化硅为核材料,通过 1,3,5-均苯三甲酰基间苯二胺(Tp)和对苯二胺(Pa-1)的共价偶联制备 COF-TpPa-1@SiO 复合微球,制备了β-酮亚胺 COF-TpPa-1@SiO 复合微球。所得微球具有形貌均匀、单分散性好、比表面积大、粒径分布窄、稳定性好等特点。由于 COF-TpPa-1 结构中含有多种功能基团,微球可以提供多种相互作用,如 COFs 与分析物之间的疏水、π-π堆积和电子供体-受体(EDA)相互作用。因此,COF-TpPa-1@SiO 复合微球可用作 HPLC 分离的混合模式固定相。通过在各种 HPLC 模式下(包括反相液相色谱(RPLC)、亲水作用色谱(HILIC)和 RPLC/HILIC 混合模式色谱)分离极性和非极性溶质以及异构体,研究了 COF-TpPa-1@SiO 填充柱的色谱性能和保留机理。结果表明,在 RPLC 模式下成功分离了非极性烷基苯同系物、多环芳烃(PAHs)和极性胺类和酚类。四种碱基在流动相中 ACN 浓度的保留因子“U”形曲线表明,溶质在柱上的保留遵循 RPLC/HILIC 混合模式机制。与传统的 C18 柱相比,COF-TpPa-1@SiO 柱在分离不同极性的分析物时具有更高的分离效率、稳定性、重复性和重现性。该柱通过π-π相互作用增强了对 PAHs 和异构体的芳香性、形状和平面选择性,并由于 EDA 效应提高了对缺电子化合物的分离效率。最后,该柱成功用于分离和检测土壤中 5 种苯脲类除草剂(PUHs)的残留。所有这些结果表明 COFs 在色谱应用中的潜力。