Mixed ligand cobalt (ii) complex and its preparation method and application
A technology of mixing ligands and complexes, applied in the direction of cobalt organic compounds, the size/direction of the magnetic field, etc., can solve problems such as limited, and achieve the effects of good solubility, high thermal stability and high yield
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Embodiment 1
[0036] Synthesis of 1,2,4-triazole and 5-sulfoisophthalic acid mixed ligand cobalt(II) complex A:
[0037] 1,2,4-triazole (0.2 mmol, 14.0 mg), m-benzene two Formic acid-5-sodium sulfonate (0.1 mmol, 27.0 mg) and cobalt nitrate hexahydrate (0.1 mmol, 29.0 mg) were dissolved in a mixed solution of twice distilled water (6.0 mL) and methanol (4.0 mL), and washed with three Ethylamine was used to adjust the pH to 6, and after stirring for a few minutes, it was sealed in a hydrothermal kettle. After incubating at 170° C. for 3 days, the temperature was programmed to cool down to room temperature to obtain a purple-red bulk single crystal, which was then washed with ethanol and dried in air. See figure 1 3D structure diagram.
Embodiment 2
[0039] Synthesis of 1,2,4-triazole and 5-sulfoisophthalic acid mixed ligand cobalt(II) complex B:
[0040] 1,2,4-Triazole (0.2 mmol, 14.0 mg), sodium 5-sulfoisophthalate (0.1 mmol, 27.0 mg) and cobalt nitrate hexahydrate (0.15 mmol, 44.0 mg) were dissolved In a mixed solution of double-distilled water (5.0 mL) and methanol (5.0 mL), adjust the pH to 7 with triethylamine, stir for several minutes, and seal it into a hydrothermal kettle. After being incubated at 165°C for 3 days, the temperature was programmed to cool down to room temperature to obtain a pink blocky single crystal, which was then washed with ethanol and dried, see figure 1 3D structure diagram.
Embodiment 3
[0042] Synthesis of 1,2,4-triazole and 5-sulfoisophthalic acid mixed ligand cobalt(II) complex C:
[0043] 1,2,4-triazole (0.2 mmol, 14.0 mg), m-benzene two Formic acid-5-sodium sulfonate (0.1 mmol, 27.0 mg) and cobalt nitrate hexahydrate (0.15 mmol, 44.0 mg) were dissolved in a mixed solution of twice distilled water (6.0 mL) and ethanol (4.0 mL), and washed with three Ethylamine was used to adjust the pH to 7, and after stirring for a few minutes, it was sealed in a hydrothermal kettle. After incubating at 160° C. for 3 days, the temperature was programmed to cool down to room temperature to obtain a pink bulk single crystal, which was then washed with ethanol and dried. See figure 1 3D structure diagram.
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