Ultrathin nanosheets of luminescent metal-organic frameworks or coordination polymers have been widely used for sensing ions, solvents and biomolecules but, as far as we are aware, not yet used for temperature sensing. Herein we report two luminescent uranyl phosphonates based on 2-(phosphonomethyl)benzoic acid (2-pmbH), namely (UO)(2-pmbH) (1) and (HO)[(UO)(2-pmb)(2-pmbH)] (2). The former has a supramolecular layer structure, composed of chains of corner-sharing {UO} octahedra and {POC} tetrahedra which are connected by hydrogen bonds between phosphonate and carboxylic groups. Compound 2 possesses a unique 2D anionic framework structure, where the inorganic uranyl phosphonate chains made up of {UO} and {POC} polyhedra are cross-linked by 2-pmb ligands. The carboxylic groups of 2-pmbH ligands are pendant on the two sides of the layers and form hydrogen bonds between the layers. Both compounds can be exfoliated in acetone a top-down freeze-thaw method, resulting in nanosheets of two-layer thickness. Interestingly, the photoluminescence (PL) of 1 and 2 is highly temperature sensitive. Variable temperature PL studies revealed that compounds 1 and 2 can be used as thermometers in the temperature ranges 120-300 K and 100-280 K, respectively. By doping the nanosheets into polymer matrix, 1-ns@PMMA and 2-ns@PMMA were prepared. The PL intensity of 1-ns@PMMA is insensitive to temperature, unlike that of the bulk sample. While 2-ns@PMMA exhibits similar temperature-dependent luminescence behaviour to its bulk counterpart, thereby enabling its potential application as a thermometer in the temperature range 100-280 K.
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http://dx.doi.org/10.1039/d1dt02977k | DOI Listing |
Acc Chem Res
October 2024
State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Collaborative Innovation Centre of Advanced Microstructures, Nanjing University, Nanjing 210023, China.
ConspectusPorous metal phosphonate frameworks (PMPFs) as a subclass of metal-organic frameworks (MOFs) have promising applications in the fields of gas adsorption and separation, ion exchange and storage, catalysis, sensing, etc. Compared to the typical carboxylate-based MOFs, PMPFs exhibit higher thermal and water stability due to the strong coordination ability of the phosphonate ligands. Despite their robust frameworks, PMPFs account for less than 0.
View Article and Find Full Text PDFNanomaterials (Basel)
May 2024
State Key Laboratory of Nuclear Resources and Environment, East China University of Technology, Nanchang 330013, China.
A novel biomass-based magnetic nanoparticle (FeO-P-CMC/PAMAM) was synthesized by crosslinking carboxymethyl chitosan (CMC) and poly(amidoamine) (PAMAM), followed by phosphorylation with the incorporation of magnetic ferric oxide nanoparticles. The characterization results verified the successful functionalization and structural integrity of the adsorbents with a surface area of . 43 m/g.
View Article and Find Full Text PDFInorg Chem
May 2024
Department of Chemistry, College of Science, Qassim University, Buraydah Al-Mulida, P.O. Box: 6644, Buraydah 51452, Saudi Arabia.
Ionic liquids (ILs) have significant potential for eco-friendly extraction of uranium from aqueous solutions, which is critical for nuclear technology, fuel cycle management, and environmental protection. This study examines the impact of the adjustable hydrophobic/hydrophilic properties of ILs on the removal of uranium(VI) (UO) from aqueous solutions utilizing both a novel hydrophilic IL (1-butoxyethyl-1-methylmorpholinium butoxyethylphosphite - Mor-BOEP) and 1-heptyl-1-methylmorpholinium heptylphosphite (Mor-HP) as an example of a hydrophobic IL with a similar structure. The transfer mechanism of uranyl ions from water to organic or solid phases closely depends on the physicochemical properties of ILs, especially their hydrophobicity.
View Article and Find Full Text PDFJ Comput Chem
January 2024
Indira Gandhi Centre for Atomic Research, Kalpakkam, India.
The conventional argument that extraction efficiency depends on the "basicity of the phosphoryl oxygen" is thoroughly examined in this study. The analysis involves studying the electronic structures of various ligands, such as phosphate, phosphonate, phosphinate, and phosphine oxide, as well as variations in their alkyl chain length, and their corresponding uranium complexes. The studies revealed a significant amount of destabilizing strain and steric repulsion for ligands having longer alkyl chains upon complexation.
View Article and Find Full Text PDFInorg Chem
July 2023
Institute of Nuclear Physics and Chemistry (INPC), China Academy of Engineering Physics (CAEP), Mianyang, 621900 Sichuan, China.
Metal phosphonate frameworks (MPFs) consisting of tetravalent metal ions and aryl-phosphonate ligands feature a large affinity for actinides and excellent stabilities in harsh aqueous environments. However, it remains elusive how the crystallinity of MPFs influences their performance in actinide separation. To this end, we prepared a new category of porous, ultrastable MPF with different crystallinities for uranyl and transuranium separation.
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