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This study reports on two multicomponent hybrid supramolecular assemblies by integrating polyoxometalates (POMs) and cyclodextrins (CDs) through noncovalent interactions, namely, (NH)KH[{FeMo(OH)O}(γ-CD)]·26HO (denoted as {FeMo}(γ-CD), ) and (NH)KH[{FeMo(OH)O}{MoO}(γ-CD)]·29HO (denoted as {Mo}{FeMo}(γ-CD), ). represents a two-component open framework built from Anderson-type {FeMo} units by interacting with the external surface of γ-CD while could be viewed as a three-component hybrid when inner cavities of (γ-CD) species in are filled by the formed Lindqvist-type {MoO} anions driven by a chaotropic effect. This pair of hybrid supramolecular assemblies provides a molecular-level platform for exploring the structure-property relationships related to proton conductivity. As expected, the proton conductivity of remains a 3-fold enhancement compared to that of , which may be arisen from the increasing numbers of "proton-carrier" molecules due to the introduction of {MoO} guest within the macrocyclic host matrix. This work paves the way for engineering multifunctional POM-CD-based supramolecular frameworks featuring tailor-made properties controlled by inorganic POM entities through a chaotropic effect.
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http://dx.doi.org/10.1021/acs.inorgchem.5c01892 | DOI Listing |
J Phys Chem C Nanomater Interfaces
September 2025
Institute of Inorganic Chemistry of the Czech Academy of Sciences, Husinec-Řež 1001, 250 68 Řež, Czech Republic.
Coordination polymers (CPs) are versatile materials formed by metal ions and organic ligands, offering a broad range of structural and functional possibilities. Phosphonates and phosphinates are particularly attractive ligands for CPs due to their multiple binding sites, varied coordination geometries, and ability to form robust network structures. Phosphonates, considered harder ligands, form strong bonds with hard metals such as Fe, while phosphinates offer additional versatility due to the varied pendant groups on phosphorus.
View Article and Find Full Text PDFNatl Sci Rev
September 2025
Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials, Department of Chemistry, University of Science and Technology Beijing, Beijing 100083, China.
Covalent organic frameworks (COFs) have great potential as versatile platforms for proton conduction. However, the commonly applied 2D COFs that are easy to design and synthesize have only 1D channels for proton conduction, limiting the formation of continuous hydrogen bonds due to the anisotropy between their crystalline grains. Herein, we report a strategy to construct 3D channels in 2D COFs by using rotaxane structures and eliminate the strong interlayer π-π interactions, facilitating the formation of smooth 3D proton-transfer pathways during guest doping.
View Article and Find Full Text PDFOrg Biomol Chem
September 2025
Glycosystems Laboratory, Instituto de Investigaciones Químicas (IIQ), Centro de Investigaciones Científicas Isla de La Cartuja, CSIC and Universidad de Sevilla, 41092 Sevilla, Spain.
In this paper, we present the NMR analysis of multivalent compounds displaying chondroitin sulfate E (CS-E) disaccharide ligands and their interaction with langerin. The disaccharides correspond to the two alternative sequences of CS-E: GlcA-GalNAc and GalNAc-GlcA. Firstly, we studied the conformation of the two corresponding series of glycodendrimers free in solution and in the presence of langerin.
View Article and Find Full Text PDFInt J Pharm Pract
September 2025
Department of Pharmaceutical Care, Faculty of Pharmacy, Chiang Mai University, Suthep Road, Suthep, Mueang, Chiang Mai 50200, Thailand.
Objectives: Proton pump inhibitors (PPIs) are commonly used among these patients to prevent upper gastrointestinal bleeding (UGIB) in anticoagulated patients. However, their clinical benefits among patients receiving OACs with a history of UGIB remain inconclusive. This study aimed to summarize the clinical benefits of PPIs for the secondary prevention of recurrent UGIB among patients using OACs.
View Article and Find Full Text PDFChem Asian J
September 2025
School of Chemistry and Chemical Engineering, Hainan University, Haikou, 570228, China.
Molecules that exhibit excited-state intramolecular proton transfer (ESIPT) have demonstrated great promise in fluorescent probes. The electronic effect of substituents has an important influence on the ESIPT process. In this study, we investigated the effects of substituents on the ESIPT mechanism and the photophysical behavior of single-benzene fluorophore (SBF) derivatives with computational chemistry methods.
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