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Background: Self-crosslinked poly(ionic liquid)s (CPIs), a subset of ionic liquids, are emerging functional polymeric materials with broad applications in catalysis and sensor technology. However, there are scant reports on the use of CPIs as high-performance liquid chromatography (HPLC) stationary phases. Fluorinated materials, noted for their unique physicochemical properties, have recently drawn interest in purification and separation fields.
Results: In this work, self-crosslinked poly(ionic liquid)s were first employed to prepare a stationary phase (Sil-CPIs) for HPLC, and fluorine functionalization (Sil-CPIs-F) was achieved with 1H,1H,2H,2H-heptadecafluorodecyl acrylate (PFOEA).The impact of chromatographic conditions on retention demonstrated that both Sil-CPIs and Sil-CPIs-F could operate in a multimodal manner, with various analytes (including nucleobases, organic acids, and sulfonamide drugs) being effectively separated under different modes. Outstanding repeatability (RSD ≤0.67 %) and column efficiency (127,010 plates/m) were attained. Fluorine functionalization enhanced the separation performance of the poly(ionic liquid)s stationary phase, endowing it with superior selectivity and separation efficiency towards phenolic isomers and complex samples. Thermodynamic investigations revealed the differences in the retention mechanisms of Sil-CPIs and Sil-CPIs-F, while the linear solvation energy relationship (LSER) more specifically indicated that fluorine modification intensified dipole-dipole interaction and hydrophobic effect of Sil-CPIs. The column with better performance was used to detect chlorpheniramine maleate in pediatric cold medicine and dehydroacetic acid in 6 food samples (including bread, dessert, pastry, instant noodle seasoning packet, fruit and vegetable juice, and pickled turnip), with recovery rate ranging from 99.4 % to 104.67 %, meeting the detection requirements for actual samples.
Significance: This study confirms the modifiability of self-crosslinked poly(ionic liquid)s stationary phase with 3D reticulated structures, and demonstrates that the introduction of fluorinated monomer can enhance the comprehensive separation capabilities of Sil-CPIs. The potential application value of Sil-CPIs-F in the analysis of multi-component samples and actual detection has been highlighted.
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http://dx.doi.org/10.1016/j.aca.2025.344146 | DOI Listing |
Soft Matter
September 2025
Transport phenomena, Chemical engineering Department, Faculty of applied sciences, Delft University of Technology, Van der Maasweg 9, 2629HZ Delft, The Netherlands.
Polymer membranes are prime candidates for separation and purification processes, with their functionality enhanced by nanoparticle incorporation and diverse polymer structures. Poly(ionic liquids) (PILs), highly charged electrolyte-like polymers, are gaining interest as membrane polymer matrices. Embedding photocatalytic nanoparticles enables water purification through filtration and degradation reactions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Key Laboratory of High-Performance Plastics, Ministry of Education, National & Local Joint Engineering Laboratory for Synthesis Technology of High-Performance Polymers, College of Chemistry, Jilin University, Changchun, 130012, China.
Thanks to the unique rigid conformation and designable side-chain structure, helical polymers are starting to be more widely considered as ideal electrode materials in secondary batteries. In this study, a series of helical poly(isocyanide anthraquinones) (PIC-AQs), including PIC-1AQ and PIC-2AQ, were designed and synthesized via living polymerization using a palladium catalyst (Pd-II). The polymers feature a helical polyisocyanide main chain and anthraquinone (AQ) pendants, offer high yields (approximately 90%), controlled number-average molecular weight (M), and a low polymer dispersity index (PDI).
View Article and Find Full Text PDFPolymers (Basel)
August 2025
Department of Chemistry, School of Sciences and Humanities, Nazarbayev University, Astana 010000, Kazakhstan.
Over the past few decades, lithium-ion batteries (LIBs) have gained significant attention due to their inherent potential for environmental sustainability and unparalleled energy storage efficiency. Meanwhile, polymer electrolytes have gained popularity in several fields due to their ability to adapt to various battery geometries, enhanced safety features, greater thermal stability, and effectiveness in reducing dendrite growth on the anode. However, their relatively low ionic conductivity compared to liquid electrolytes has limited their application in high-performance devices.
View Article and Find Full Text PDFNat Commun
August 2025
School of Materials Science and Engineering, Nanyang Technological University, Singapore, Singapore.
Dielectric elastomer actuators (DEAs) exhibit large actuation strains, lightweight, and fast response, making them a promising candidate for soft robotics and soft grippers. Ionogels have been used as the electrodes in DEAs to offer thermostability and self-healability, however, typically the elastic modulus of the self-healing ionogel electrodes is of several tens of kPa (or higher), limiting the actuation strain performance and self-healing speed of the DEA. In this work, a poly(ionic liquid) (PIL) electrode with an ultralow elastic modulus of 3.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2025
Laboratoire Charles Coulomb (L2C), Université de Montpellier, CNRS, 34095 Montpellier, France.
Understanding the molecular structure of mesoporous solid ionic systems is essential for optimizing their macroscopic properties, such as enhanced ionic transport for energy applications and improved mechanical flexibility. These systems can be synthesized efficiently using "one-pot" conditions, where mesopores form via the microphase separation of a templating ionic liquid. Furthermore, incorporating poly(ionic liquid)s can improve structural connectivity and tailor the mechanical strength of the material.
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