11 research outputs found

    Tuning the Structure and Magnetism of Heterometallic Sodium(1+)–Cobalt(2+) Formate Coordination Polymers by Varying the Metal Ratio and Solvents

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    Three new heterometallic formate coordination polymers formulated as [Na<sub>2</sub>Co­(HCOO)<sub>4</sub>]<sub>∞</sub> (<b>1</b>), [NaCo­(HCOO)<sub>3</sub>]<sub>∞</sub> (<b>2</b>), and [Na<sub>2</sub>Co<sub>7</sub>(HCOO)<sub>16</sub>]<sub>∞</sub> (<b>3</b>) were obtained by adjusting the solvent and ratio of the reactants. In <b>1</b>, a (4,4) cobalt formate layer is formed and the sodium ions connect the layers to form a three-dimensional (3D) framework. In <b>2</b>, each formate ligand binds two Co<sup>2+</sup> and two Na<sup>+</sup> ions with a syn,syn,anti,anti coordination mode to form a chrial network with 4,6-connected topology. <b>3</b> is a Na<sup>+</sup>-ion-linked 3D framework based on the cobalt formate layer, which has a 10-membered metal ring. Magnetic studies indicate the existence of ferromagnetic interactions between adjacent Co<sup>2+</sup> ions in <b>1</b>, while dominating antiferromagnetic couplings in <b>2</b> and <b>3</b>

    Two Cobalt-diphosphonates Templated by Long-Chain Flexible Amines: Synthesis, Structures, Proton Conductivity, and Magnetic Properties

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    Two new cobalt-diphosphonates templated by protonated 1,2-bis­(3-aminopropylamino)­ethane (BAPEN), (C<sub>8</sub>N<sub>4</sub>H<sub>26</sub>)<sub>0.5</sub>·[Co­(HEDP)]·H<sub>2</sub>O (<b>1</b>) and (C<sub>8</sub>N<sub>4</sub>H<sub>26</sub>)·[Co<sub>2</sub>(HEDP)<sub>2</sub>(H<sub>2</sub>O)<sub>2</sub>]·5H<sub>2</sub>O (<b>2</b>), were hydrothermally prepared (HEDP = CH<sub>3</sub>C­(OH)­(PO<sub>3</sub>)<sub>2</sub>, 1-hydroxyethylidenediphosphonate). Compounds <b>1</b> and <b>2</b> exhibit anionic 1D Co-HEDP chain and 2D Co-HEDP layer structure, respectively. The structure diversities from 1D chain to 2D layer was realized by adjusting the synthetic parameters. Their magnetism and proton conduction have been studied. Magnetic measurements indicated that the title compounds exhibit weak magnetic interactions. Compounds <b>1</b> and <b>2</b> feature a proton conductivity of 3.57 × 10<sup>–4</sup> and 9.43 × 10<sup>–5</sup> S cm<sup>–1</sup> at 100% relative humidity and 65 °C, respectively

    3D Gd<sup>III</sup> Complex Containing Gd<sub>16</sub> Macrocycles Exhibiting Large Magnetocaloric Effect

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    Hydrothermal synthesis of Gd<sub>2</sub>O<sub>3</sub> and iminodiacetic acid (H<sub>2</sub>IDA) yields a three-dimensional (3D) complex {[Gd<sub>2</sub>(IDA)<sub>3</sub>]·2H<sub>2</sub>O}<sub><i>n</i></sub> (<b>1</b>) including Gd<sub>16</sub> macrocycles. Magnetic investigation indicates the presence of weak antiferromagnetic interaction between Gd<sup>III</sup> ions and a large magnetocaloric effect with −Δ<i>S</i><sub>m</sub><sup>max</sup> = 40.6 J kg<sup>–1</sup> K<sup>–1</sup>

    3D Inorganic Cuprous Iodide Open-Framework Templated by In Situ <i>N</i>‑Methylated 2,4,6-Tri(4-pyridyl)-1,3,5-triazine

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    A novel 3D inorganic cuprous iodide framework templated by in situ <i>N</i>-methylated 2,4,6-tri­(4-pyridyl)-1,3,5-triazine (TPT) was solvothermally prepared and structurally characterized. The title compound bearing chiral cuprous iodide chains as building units is the first 3D extended framework with the TPT-derivatives as template. The UV–vis diffuse-reflectance measurement reveals that <b>1</b> possesses semiconductor behavior with band gaps of 1.35 eV. The photoluminescent property of <b>1</b> has also been studied

    3D Gd<sup>III</sup> Complex Containing Gd<sub>16</sub> Macrocycles Exhibiting Large Magnetocaloric Effect

    No full text
    Hydrothermal synthesis of Gd<sub>2</sub>O<sub>3</sub> and iminodiacetic acid (H<sub>2</sub>IDA) yields a three-dimensional (3D) complex {[Gd<sub>2</sub>(IDA)<sub>3</sub>]·2H<sub>2</sub>O}<sub><i>n</i></sub> (<b>1</b>) including Gd<sub>16</sub> macrocycles. Magnetic investigation indicates the presence of weak antiferromagnetic interaction between Gd<sup>III</sup> ions and a large magnetocaloric effect with −Δ<i>S</i><sub>m</sub><sup>max</sup> = 40.6 J kg<sup>–1</sup> K<sup>–1</sup>

    Synthesis and Magnetic Properties of a Series of Octanuclear [Fe<sub>6</sub>Ln<sub>2</sub>] Nanoclusters

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    The reaction of polydentate ligand Bis-tris propane {(CH<sub>2</sub>OH)<sub>3</sub>CNH­(CH<sub>2</sub>)<sub>3</sub>NHC­(CH<sub>2</sub>OH)<sub>3</sub>} with Ln­(NO<sub>3</sub>)<sub>3</sub>·6H<sub>2</sub>O and Fe<sub>3</sub>O precursor resulted in the formation of a series of Fe<sub>6</sub>Ln<sub>2</sub> nanoclusters. Magnetic measurements indicate that the Fe<sub>6</sub> core exhibits ferrimagnetic behavior, and slow magnetic relaxation was observed in Fe<sub>6</sub>Dy<sub>2</sub> and Fe<sub>6</sub>Tb<sub>2</sub>

    Large Heterometallic Dy<sub>12</sub>Na<sub>6</sub> Cage-like Cluster Supported by in Situ Generated Ligand

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    A novel heterometallic cluster, Dy<sub>12</sub>Na<sub>6</sub>, has been prepared and characterized. It represents an unprecedented high-nuclearity alkali-metal-Ln cluster with a cage-like shape. In situ generated ligands participated in the formation of the heterometallic cluster. Magnetic measurements suggest that Dy<sub>12</sub>Na<sub>6</sub> shows slow magnetic relaxation at low temperature

    A Spin-Canted Polynuclear Manganese Complex Comprised of Alternating Linkage of Cyclic Tetra-and Mononuclear Fragments

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    A polynuclear manganese complex composed of alternating cyclic tetramer and monomer has been solvothermally prepared and magnetically characterized. Magnetic analyses indicate that the title compound shows spin-canting behavior

    A Spin-Canted Polynuclear Manganese Complex Comprised of Alternating Linkage of Cyclic Tetra-and Mononuclear Fragments

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    A polynuclear manganese complex composed of alternating cyclic tetramer and monomer has been solvothermally prepared and magnetically characterized. Magnetic analyses indicate that the title compound shows spin-canting behavior

    An Unprecedented Decanuclear Gd<sup>III</sup> Cluster for Magnetic Refrigeration

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    An unprecedented decanuclear Gd<sup>III</sup> cluster composed of the [Gd<sub>10</sub>(μ<sub>3</sub>-OH)<sub>8</sub>]<sup>22+</sup> core has been hydrothermally synthesized. Magnetic analyses indicate that this complex shows weak antiferromagnetic behavior with a relatively large magnetocaloric effect (−Δ<i>S</i><sub>m</sub><sup>max</sup> = 31.22 J kg<sup>–1</sup> K<sup>–1</sup>)
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