Hydrophobic (water-immiscible) ionic liquids (ILs) are frequently used as organic phase in solvent extraction studies. These biphasic IL/water extraction systems often also contain metal salts or mineral acids, which can significantly affect the IL trough (un)wanted anion exchange and changes in the solubility of IL in the aqueous phase. In the case of thermomorphic systems, variations in the cloud point temperature are also observed. All these effects have important repercussions on the choice of IL, suitable for a certain extraction system. In this paper, a complete overview of the implications of metal salts on biphasic IL/water systems is given. Using the Hofmeister series as a starting point, a range of intuitive prediction models are introduced, supported by experimental evidence for several hydrophobic ILs, relevant to solvent extraction. Particular emphasis is placed on the IL betainium bis(trifluoromethylsulfonyl)imide [Hbet][Tf2N]. The aim of this work is to provide a comprehensive interpretation of the observed effects of metal salts, so that it can be used to predict the effect on any given biphasic IL/water system instead of relying on case-by-case reports. These prediction tools for the impact of metal salts can be useful to optimize IL synthesis procedures, extraction systems and thermomorphic properties. Some new insights are also provided for the rational design of ILs with UCST or LCST behavior based on the choice of IL anion.
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Carbohydr Polym
March 2025
Key Laboratory of Thorium Energy, Shanghai Institute of Applied Physics, Chinese Academy of Science, No. 2019 Jialuo Road, Shanghai 201800, China.
Ionic conductive hydrogels have attracted great attention due to their good flexibility and conductivity in flexible electronic devices. However, because of the icing and water loss problems, the compatibility issue between the mechanical properties and conductivity of hydrogel electrolytes over a wide temperature range remains extremely challenging to achieve. Although, antifreezing/water-retaining additives could alleviate these problems, the reduced performance and complex preparation methods seriously limit their development.
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Science, Faculty of Science, Yamagata University, 1-4-12 Kojirakawa, Yamagata 990-8560, Japan.
Two 3D/2D anionic metal-organic frameworks (MOFs), [Cu(HL)] () and [Mn(L)(DMF)] ( (DMF = ,-dimethylformamide), were synthesized by the solvothermal reaction of metal salts and 5'-(4-carboxyphenyl)-2',4',6'-triethyl-[1,1':3',1″-terphenyl]-4,4″-dicarboxylic acid (HL). Single-crystal X-ray diffraction analyses revealed that complex shows three-dimensional (3D) frameworks with a (3,6)-connected 3-fold interpenetrated topology with the Schläfli symbols of {4.6}{4.
View Article and Find Full Text PDFJ Chem Phys
January 2025
School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, Singapore 637551, Singapore.
Eukaryotic DNA is packaged in the cell nucleus into chromatin, composed of arrays of DNA-histone protein octamer complexes, the nucleosomes. Over the past decade, it has become clear that chromatin structure in vivo is not a hierarchy of well-organized folded nucleosome fibers but displays considerable conformational variability and heterogeneity. In vitro and in vivo studies, as well as computational modeling, have revealed that attractive nucleosome-nucleosome interaction with an essential role of nucleosome stacking defines chromatin compaction.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
College of Pharmaceutical Sciences, Ritsumeikan University, Kusatsu 525-8577, Shiga, Japan.
We have developed transition-metal-free synthetic methodologies for dibenzoxazepinones utilizing salicylamides as starting materials and employing two distinct types of successive hypervalent iodine-mediated arylocyclizations. This synthetic protocol encompasses selective phenol -arylation of salicylamides with diaryliodonium salts, followed by electrophilic aromatic amination utilizing chemically or electronically generated hypervalent iodine reagents in the second stage of the process.
View Article and Find Full Text PDFInorg Chem
January 2025
College of Environment and Materials Engineering, Yantai University, Yantai 264005, China.
As an attractive optical/heat dynamic management technology, reversible metal electrodeposition/dissolution electrochromism (RME-EC) shows many advantages, including high optical modulation amplitude, wide modulation band, and color neutrality, but also suffers from performance degradation because of uneven dendritic metal deposition as well as the formation/accumulation of isolated metal debris. In this paper, a facile RME-EC system is established in a green and affordable aqueous electrolyte, by making good use of the nondendritic Ni-Cu codeposition. Furthermore, an in situ self-healing strategy is further established by activating the Br/Br couple of the Br-containing electrolyte to improve the EC performance.
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