Tetrazolyl cobalt (II) complex magnetic material and preparation method and application thereof
A technology of coordination polymers and tetrazolium, which is applied in the fields of magnetism of organic materials/organic magnetic materials, cobalt organic compounds, magnetic recording, etc., can solve problems such as limited research, achieve good reproducibility, high yield, The effect of high thermal stability
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Embodiment 1
[0027] Synthesis of 5-methyl-1H-tetrazolium and isophthalic acid mixed ligand cobalt(II) coordination polymer A:
[0028] Dissolve 5-methyl-1H-tetrazole (0.3 mmol, 25.2 mg), isophthalic acid (0.2 mmol, 33.2 mg) and cobalt nitrate hexahydrate (0.3 mmol, 87.3 mg) in double distilled water (7.0 mL) and ethanol (3.0 mL), adjust the pH to 4 with triethylamine, stir for several minutes, and seal it into a hydrothermal kettle. After being incubated at 180° C. for three days, the temperature was programmed to cool down to room temperature to obtain a red bulky single crystal, which was then washed with ethanol and dried in air. See figure 1 crystal structure diagram.
Embodiment 2
[0030] Synthesis of 5-methyl-1H-tetrazolium and isophthalic acid mixed ligand cobalt(II) coordination polymer B:
[0031] Dissolve 5-methyl-1H-tetrazolium (0.3 mmol, 25.2 mg), isophthalic acid (0.2 mmol, 33.2 mg) and cobalt nitrate hexahydrate (0.3 mmol, 87.3 mg) in double distilled water (7.0 mL) and ethanol (3.0 mL), adjust the pH to 4 with triethylamine, stir for a few minutes and seal it into a hydrothermal kettle. After being incubated at 190° C. for three days, the temperature was programmed to cool down to room temperature to obtain a red blocky single crystal, which was then washed with ethanol and dried in air. See figure 1 crystal structure diagram.
Embodiment 3
[0033] Synthesis of 5-methyl-1H-tetrazolium and isophthalic acid mixed ligand cobalt(II) coordination polymer C:
[0034] Dissolve 5-methyl-1H-tetrazole (0.3 mmol, 25.2 mg), isophthalic acid (0.2 mmol, 33.2 mg) and cobalt nitrate hexahydrate (0.35 mmol, 101.9 mg) in double distilled water (7.0 mL) and ethanol (3.0 mL), adjust the pH to 5 with triethylamine, stir for several minutes, and seal it into a hydrothermal kettle. After being incubated at 180° C. for three days, the temperature was programmed to cool down to room temperature to obtain a red bulky single crystal, which was then washed with ethanol and dried in air. See figure 1 crystal structure diagram.
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