Reaction of A-alpha-PW(9)O(34)(9)(-) with YCl(3) in an aqueous Na(2)CO(3) solution produces a dianion-encapsulated A-type sandwich polyoxometalate, (YOH(2))(3)(CO(3))(A-alpha-PW(9)O(34))(2)(11)(-). The X-ray structure of this complex reveals that three Y(III) ions are sandwiched between two A-alpha-PW(9)O(34)(9)(-) moieties and that a carbonate dianion is encapsulated in the same plane as the three Y(III) atoms. The oxygen atoms of the CO(3)(2)(-) are sitting at the midpoints of the sides of the triangle formed by the three Y(III) ions. (31)P and (13)C NMR studies confirm that this complex is significantly more stable than the analogous A-type sandwich polyoxometalates containing divalent metals.
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http://dx.doi.org/10.1021/ic0350842 | DOI Listing |
Inorg Chem
November 2024
School of Chemistry and Chemical Engineering, Jiangxi Provincial Key Laboratory of Functional Crystalline Materials Chemistry, Jiangxi University of Science and Technology, Ganzhou, Jiangxi Province 341000, P. R. China.
Three mononuclear Dy compounds [DyL(PhSiO)][BPh]·MeCN·2HO (), [DyL(PhSiO)][BPh]·CHOH·HO (), and [DyL(PhSiO)(OAc)][BPh]·CHOH·3HO () and their corresponding Y diluted analogues [DyYL(PhSiO)][BPh]·MeCN·2HO (), [DyYL(PhSiO)][BPh]·CHOH·HO (), and [DyYL(PhSiO)(OAc)][BPh]·CHOH·3HO () were synthesized with hexaazamacrocyclic Schiff base ligands as an equatorial ligand. The substituents in the equatorial hexaazamacrocyclic Schiff base ligand show a significant effect on the replacement of the axial ligands. Compounds , , and are typical zero dc field single-molecule magnets with effective energy barriers () of 1092(6), 946.
View Article and Find Full Text PDFInorg Chem
September 2024
Department of Inorganic and Analytical Chemistry, University of Geneva, 30 quai E. Ansermet, CH-1211 Geneva 4, Switzerland.
Pseudo-octahedral CrN chromophores hold a unique appeal for low-energy sensitization of NIR lanthanide luminescence due to their exceptionally long-lived spin-flip excited states. This allure persists despite the obstacles and complexities involved in integrating both elements into a metallosupramolecular assembly. In this work, we have designed a structurally optimized heteroleptic Cr building block capable of binding rare earths.
View Article and Find Full Text PDFAnal Methods
February 2024
School of Resources and Environmental Engineering, Jiangxi University of Science and Technology, Kejia Road 156, Ganzhou 341000, Jiangxi, China.
In the aqueous phase, ion-imprinted materials exhibit excellent selective adsorption properties for specific ions, but their complicated preparation process and large amount of crosslinker consumption limit their application. In this study, ion-imprinted chitosan (IIP-CS) was prepared by a simple one-step hydrothermal method without a cross-linking agent for the efficient adsorption of trace amounts of Al(III) from a rare earth solution. The structures and morphology of IIP-CS were analyzed by FT-IR, SEM, and XRD.
View Article and Find Full Text PDFYttrium is an important rare earth element and is widely used in fields such as special glass preparation, metallurgy, and materials science. However, it is difficult to recover yttrium ion waste from dilute solutions with traditional processes, resulting in a significant waste of rare earth resources. The simple, effective, and easy-to-operate adsorption method is the most promising method for recovering yttrium, which is of great significance for sustainable development of the rare earth industry.
View Article and Find Full Text PDFInorg Chem
August 2023
Department of Chemistry, Tsinghua University, Beijing 100084, P.R. China.
Multifunctional single-molecule magnets (SMMs) have sparked great interest, but chiral SMMs obtained via spontaneous resolution are rarely reported. We synthesized a series of chiral trinuclear hepta-coordinate lanthanide complexes [ZnLn] ( for Dy, for Tb, for Gd, and for DyY) using the achiral flexible ligand HL (2,2'-[1,2-ethanediylbis[(ethylimino)methylene]]bis[3,5-dimethylphenol]). The complexes crystallize in the chiral 6 group space, and two enantiomers of different chirality are spontaneously resolved.
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