3d-4f heteronuclear metal magnetic complex and preparing method and application thereof
A 3d-4f, metal complex technology, applied in the recording/reproducing, magnetic recording, instruments and other directions by optical methods, can solve the problems of weak magnetic anisotropy, difficult to improve the energy barrier of single-molecule magnets, etc., to achieve reproduction The effect of good performance, high yield, high thermal stability and phase purity
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Embodiment 1
[0030] 3 with slow relaxation behavior d -4 f Synthesis of heteronuclear metal magnetic complex A:
[0031] m-Toluic acid (0.25 mmol, 34.0 mg), o-phenanthroline (0.1 mmol, 19.8 mg) and dysprosium acetate hexahydrate (0.2 mmol, 82.3 mg) and nickel nitrate hexahydrate (0.1 mmol, 29.1 mg) was dissolved in double-distilled water (6.0 mL) and methanol (4.0 mL), and the pH of the solution was adjusted to 5 with solid sodium hydroxide, stirred for several minutes, and sealed in a hydrothermal kettle. After being incubated at 140°C for three days, at 3.0°C·h –1 The rate program cooled down to room temperature to obtain green blocky crystals, which were then washed with twice distilled water and dried in air.
Embodiment 2
[0033] 3 with slow relaxation behavior d -4 f Synthesis of heteronuclear metal magnetic complex B:
[0034] m-Toluic acid (0.2 mmol, 27.2 mg), o-phenanthroline (0.1 mmol, 19.8 mg) and dysprosium acetate hexahydrate (0.2 mmol, 82.3 mg) and ferrous sulfate heptahydrate (0.1 mmol , 27.8 mg) was dissolved in twice distilled water (6.0 mL) and methanol (4.0 mL), and the pH of the solution was adjusted to 5 with solid sodium hydroxide, and sealed in a hydrothermal kettle after stirring for several minutes. After being incubated at 160°C for three days, at 3.0°C·h –1 The rate program cooled down to room temperature to obtain red blocky crystals, which were then washed with twice distilled water and dried in air.
Embodiment 3
[0036] 3 with slow relaxation behavior d -4 f Synthesis of heteronuclear metal magnetic complex C:
[0037] m-Toluic acid (0.2 mmol, 27.2 mg), o-phenanthroline (0.1 mmol, 19.8 mg) and dysprosium acetate hexahydrate (0.25 mmol, 102.9 mg) and copper nitrate trihydrate (0.1 mmol, 24.1 mg) was dissolved in double-distilled water (4.0 mL) and methanol (6.0 mL), and the pH of the solution was adjusted to 4 with solid sodium hydroxide, stirred for several minutes, and then sealed in a hydrothermal kettle. After being incubated at 120°C for three days, at 3.0°C·h –1 The rate program cooled down to room temperature to obtain blue blocky crystals, which were then washed with twice distilled water and dried in air.
[0038] (Example 1-3, A-C) prepared by the present invention has slow relaxation behavior 3 d -4 f The structural characterization of the heteronuclear metal magnetic complex is as follows:
[0039] (1) Crystal structure determination ( figure 1 )
[0040] Select a s...
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