A series of layered lanthanide phosphonates α-Ln(2-qpH)(SO4)(H2O)2 (α-Ln; Ln = Gd, Tb, Ho, Er) and β-Ln(2-qpH)(SO4)(H2O)2 (β-Ln; Ln = Gd, Tb, Ho, Er, Yb) (2-qpH2 = 2-quinolinephosphonic acid) have been synthesized and characterized. Compounds α-Ln crystallize in monoclinic space group P21/c, while compounds β-Ln crystallize in triclinic space group P1̅. Magnetic studies reveal that dominant ferromagnetic interactions are propagated between the magnetic centers in all cases. Field-induced magnetic relaxation is observed in compounds β-Er and β-Yb.
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http://dx.doi.org/10.1021/acs.inorgchem.6b00280 | DOI Listing |
Angew Chem Int Ed Engl
November 2024
Univ Brest, UMR CNRS 6521-, Laboratoire CEMCA, F 29200, Brest, France.
Ligands combining two lateral bis-pyridyl-phosphonated-pyclens were synthesized, using a flexible linear pegylated linker (L2) or a bulkier K22 crown-ether (L3). A functionalized pyridyl-phosphonated-pyclen (L1) was also prepared as a mononuclear analogue. Coordination behavior of lanthanide cations was studied via NMR titration with Lu for L1, and UV/Vis and luminescence spectroscopy with Yb for L2/L3.
View Article and Find Full Text PDFCryst Growth Des
October 2024
Departamento de Química Inorgánica, Universidad de Málaga, Campus Teatinos s/n, Málaga 29071, Spain.
Metal phosphonate-carboxylate compounds represent a promising class of materials for proton conduction applications. This study investigates the structural, thermal, and proton conduction properties of three groups of lanthanide-based compounds derived from 5-(dihydroxyphosphoryl)isophthalic acid (PiPhtA). The crystal structures, solved from X-ray powder diffraction data, reveal that groups , Ln[OP-CH(COO)(COOH)(HO)] (Ln = La, Pr), and , Ln{[OP-CH(COO)(COOH)](HO)}·2HO (Ln = La, Pr, Eu), exhibit three-dimensional frameworks, while group , Ln[OP-CH(COO)(COOH)(HO)] (Ln = Yb), adopts a layered structure with unbonded carboxylic groups oriented toward the interlayer region.
View Article and Find Full Text PDFAcc 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 PDFACS Appl Mater Interfaces
September 2024
Geochemistry Department, Sandia National Laboratories, 1515 Eubank SE Mailstop 0754, Albuquerque, New Mexico 87185-0754, United States.
Separating individual lanthanide (Ln) elements in aqueous mixtures is challenging. Ion-selective capture by porous materials, such as metal-organic frameworks (MOFs), is a promising approach. To design ion-selective MOFs, molecular details of the Ln adsorption complexes within the MOFs must be understood.
View Article and Find Full Text PDFInorg Chem
September 2024
Shandong Provincial Key Laboratory of Chemical Energy Storage and Novel Cell Technology, School of Chemistry and Chemical Engineering, Liaocheng University, Liaocheng 252059, P. R. China.
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