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Dy(III)
Results in Chemistry · 2023 · IF 2.3

Gd(III)/Dy(III)-based coordination polymers for luminescent and magnetic properties

Beibei Zheng,Chufei Miao,Han Xu,Jiaqi Lai,Meng Li,Jumei Tian

Two isostructural lanthanide-based coordination polymers, namely, {[Gd 2 (H 2 dhtp) 3 (DMF) 2 (H 2 O) 4 ]·2DMF·H 2 On ( 1 ) and {[Dy 2 (H 2 dhtp) 3 (DMF) 2 (H 2 O) 4 ]·2DMF·H 2 O}n ( 2 ) (H 4 dhtp = 2,5-dihydroxyterephthalic acid, DMF = N, N-dimethylformamide) were synthesized and structurally characterized by single-crystal X-ray diffraction, IR, powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA), and elemental analysis. Compounds 1 and 2 exhibited 3D networks and isostructures, except for the distinction of the metal ion. Magnetic measurements indicated that complex 1 exhibited the dominating contribution at low temperature of zero-field splitting for Gd(III) materials, and the complex 2 shown the depopulation of the excited excited state for Dy(III) material. The solid luminescent properties of H 4 dhtp, 1 , and 2 displayed a blue emission band, while the solution state luminescent properties all demonstrated a green emission band. The combination of luminescence sensing and magnetism in single-phase coordination polymers may offer great potential applications in smart multitasking devices.

CAS / MDL: 19598-90-4
研究领域: 材料科学 · 化学
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2023 · IF 4.2

Solvent Extraction of Dy(III) and Nd(III) with an Unsymmetrical Pentanediamide Extractant

Zhenfeng Xiong,Ying Huang,Nan Li,Chaozhi Zhang,Yonghua Li,Zhuo Yang,Weidong Zhou,Kemei Zhou,Rong Zha,Changdong Sheng

Recovery of rare-earth elements (REEs), especially those of Dy and Nd, from Nd–Fe–B permanent magnets is crucial for sustainable development. Herein, an unsymmetrical pentanediamide extractant, N,N′-dimethyl-N,N′-didecyl-3-oxapentanediamide (DMDDOPDA), was synthesized and characterized for the effective extraction of Dy(III) and Nd(III). DMDDOPDA can form coordination bonds with metal ions because of the strong electron-donating abilities of the N and O atoms. The coordination sites might be inclined toward one side during the extraction. DMDDOPDA exhibited superior extraction performance in the HNO3 system than it did in the HCl system. The highest extraction efficiencies of Dy(III) and Nd(III) under optimal conditions were 99.9% and 99.5%, respectively, while their optimum stripping efficiencies were 100% and 85.3%, respectively. DMDDOPDA extraction of Dy(III) and Nd(III) in the four investigated diluents involved the formation of a neutral coordination complex. This study provides new insights into REE extraction using pentanediamide extractants.

CAS / MDL: 7757-82-6 108-88-3
研究领域: 化学工程 · 材料科学
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Nanomaterials · 2018 ·Vol. 8 ·期 9 ·697 · IF 3.504

Dy(III) Doped BiOCl Powder with Superior Highly Visible-Light-Driven Photocatalytic Activity for Rhodamine B Photodegradation

Jun Yang,Taiping Xie,Chenglun Liu,Longjun Xu

Dy-doped BiOCl powder photocatalyst was synthesized A one–step coprecipitation method. The incorporation of Dy3+replaced partial Bi3+in BiOCl crystal lattice system. For Rhodamine B (RhB) under visible light irradiation, 2% Dy doped BiOCl possessed highly efficient photocatalytic activity and photodegradation efficiency. The photodegradation ratio of RhB could reach 97.3% after only 30 min of photocatalytic reaction; this was more than relative investigations have reported in the last two years. The main reason was that the 4f electron shell of Dy in the BiOCl crystal lattice system can generate a special electronic shell structure that facilitated the transfer of electron from valance band to conduction band and separation of the photoinduced charge carrier. Apart from material preparation, this research is expected to provide important references for RhB photodegradation in practical applications.Keywords:Dy3+;BiOCl;photocatalyst;RhB photodegradation;doping modification

研究领域: 材料科学 · 环境科学
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CELLULOSE · 2021 ·Vol. 29 ·期 1 ·469-481 · IF 5.044

Graphene oxide and polyethyleneimine cooperative construct ionic imprinted cellulose nanocrystal aerogel for selective adsorption of Dy(III)

Zheng Xudong,Sun Wen,Li Ang,Wang Bin,Jiang Rong,Song Zhiqiang,Zhang Yuzhe,Li Zhongyu

Because of dysprosium’s unique physical and chemical properties and limited supply, the price of rare earth dysprosium has been high in recent years. Therefore, the study of the method of high efficiency selective separation of dysprosium has the double value of scientific research and practical economy. In this paper, we used periodic cellulose nanocrystals as the basic structure, polyethylenimine and graphene oxide were introduced, combined with imprinting technology, to construct a porous imprinted aerogel and use it for selective adsorption of Dy(III). The physical and chemical properties were characterized by SEM, FT-IR and TGA. It was proved that both polyethylenimine and graphene oxide were crosslinked effectively with cellulose nanocrystals. Adsorption experiments showed that the composite imprinted aerogel could selectively adsorb dysprosium effectively, and the maximum adsorption capacity for Dy(III) was 36.495 mg g −1 . The reproducibility experiment showed that aerogel had good regeneration ability. In conclusion, cellulose nanocrystal aerogel, which is environmentally friendly, efficient and repeatable, is expected to provide a new direction for the recovery of rare earth elements.

研究领域: 材料科学 · 环境科学
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TALANTA · 2018 · IF 4.244

Dy(III)-induced aggregation emission quenching effect of single-layered graphene quantum dots for selective detection of phosphate in the artificial wetlands

Shui Qin Chai,Jia Hui He,Lei Zhan,Yuan Fang Li,Chun Mei Li,Cheng Zhi Huang

Carbon quantum dots (CQDs), prepared by one-step hydrothermal treatment of perylene-3,4,9,10-tetracarboxylic dianhydride (PTCDA) and triethylamine (TEA), could be exfoliated or delaminated into single-layered graphene quantum dots (s-GQDs) with methanol for the first time, with fluorescence (FL) emission at 500 nm when excited at 417 nm. The s-GQDs, with more sufficient carboxyl groups on the surface than CQDs, could be induced to be aggregated by metal ion dysprosium (Dy 3+ ), resulting in aggregation-induced emission quenching effect subsequently. However, the presence of phosphate (PO 4 3- ) destroys the Dy 3+ -induced aggregates of s-GQDs owing to the strong coordination between Dy 3+ and PO 4 3- , inducing the FL emission recovery of the s-GQDs and providing selective detection method of PO 4 3- in the artificial wetlands with the linear range of 0.2–30 μM and determination limit of 0.1 μM (3σ).

研究领域: 分析化学 · 环境科学
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Analytical Methods · 2022 ·Vol. 14 ·期 41 ·4077-4084 · IF 3.532

Dy(III)-coordination imprinted self-assembly microspheres based on a silica core for highly sensitive and selective detection of two carbamate pesticides

Zerong Long,Shilin Shen,Hui Yuan

Carbamate (CB) pesticides possess potential carcinogenic and mutagenic activities towards humans even at very low dosages. Thus, broad-specificity probes with high sensitivity and speed are needed for multiple CB determination. This study is the first to focus on Dy3+ ions-coordinated self-assembly on a silica core using a surface imprinting procedure, for the simultaneous fluorometric detection of residues of metolcarb (MC) and pirimicarb (PC) insecticides. A simple and mild solvothermal method was applied for the preparation of fluorescent imprinted microspheres starting from 1,10-phenanthroline (Phen)-ligated Dy3+ ions to guide imprinted self-assembly of chitosan (CTS), glutaraldehyde (GA), and two carbamate pesticides (MC and PC) on the silica surface by means of coordinate bonds and hydrogen bonds. The as-prepared microspheres displayed strong fluorescence emissions via the antenna effect derived from the Phen ligand and the Schiff base oligomers for sensitizing the Dy3+ ions. An expanded in-depth mechanism study was performed on the fluorescence enhancement involving Förster resonance energy transfer (FRET) from the pesticides (donor) to the acceptor. A linear increase in fluorescence at 483 nm for MC and 574 nm for PC upon the imprinted microspheres was observed under the same 350 nm excitation wavelength. Moreover, the quantitative recognition process could be carried out simultaneously and tolerate strong distractions both from five other similar carbamate insecticides and from complicated matrices (e.g., an extract of Chrysanthemum morifolium Ramat). The detection limit was 4 ng mL−1 with a range of 10–60 ng mL−1 for MC and 0.4 ng mL−1 with a range of 1–30 ng mL−1 for PC. Further characterization of the material, including TEM, SEM, XPS, and FTIR, Raman, and fluorescence spectra, verified that the Dy3+ ions play a decisive role in promoting imprinted self-assembly around the silica core. Hence, a novel polynuclear Ln–organic imprinted probe having high selectivity, stability, and sensitivity for the detection of two carbamate insecticides is presented in this study.

研究领域: 分析化学 · 环境科学 · 食品科学
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INORGANIC CHEMISTRY · 2023 · IF 4.6

A Combined Synthetic, Magnetic, and Theoretical Study on Enhancing Ligand-Field Axiality for Dy(III) Single-Molecule Magnets Supported by Ferrocene Diamide Ligands

Kexin Yang,Rong Sun,Jingliang Zhao,Chong Deng,Bingwu Wang,Song Gao,Wenliang Huang

Molecular design is crucial for improving the performance of single-molecule magnets (SMMs). For dysprosium(III) SMMs, enhancing ligand-field axiality is a well-suited strategy to achieve high-performance SMMs. We synthesized a series of dysprosium(III) complexes, (NNTIPS)DyBr(THF)2 (1, NNTIPS = fc(NSiiPr3)2; fc = 1,1′-ferrocenediyl, THF = tetrahydrofuran), [(NNTIPS)Dy(THF)3][BPh4] (2), (NNTIPS)DyI(THF)2 (3), and [(NNTBS)Dy(THF)3][BPh4] (4, NNTBS = fc(NSitBuMe2)2), supported by ferrocene diamide ligands. X-ray crystallography shows that the rigid ferrocene backbone enforces a nearly axial ligand field with weakly coordinating equatorial ligands. Dysprosium(III) complexes 1–4 all exhibit slow magnetic relaxation under zero fields and possess high effective barriers (Ueff) around 1000 K, comparable to previously reported (NNTBS)DyI(THF)2 (5). We probed the influences of structural variations on SMM behaviors by theoretical calculations and found that the distribution of negative charges defined by rq, i.e., the ratio of the charges on the axial ligands to the charges on the equatorial ligands, plays a decisive role. Moreover, theoretical calculations on a series of model complexes 1′–5′ without equatorial ligands unveil that the axial crystal-field parameters B20 are directly proportional to the N–Dy–N angles and support the hypothesis that enhancing the ligand-field axiality could improve SMM performance.

研究领域: 无机化学 · 配位化学 · 分子磁性 · 材料科学 · 理论化学
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