5-methyl-1H-tetrazole cobalt (II) complex magnetic material, and preparation method and application thereof
A technology of tetrazolium and complexes, applied in the field of 5-methyl-1H-tetrazolium cobalt (II) complex magnetic materials and its preparation and application, can solve the problems of limited research on transition metal magnetic complexes, Achieve high yield, high thermal stability and good reproducibility
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Embodiment 1
[0029] Synthesis of 5-methyl-1H-tetrazolium and 1,2,3-trimesic acid mixed ligand cobalt(II) complex A:
[0030] 5-Methyl-1H-tetrazolium (0.2 mmol, 16.8 mg), 1,2,3-trimesic acid (0.2 mmol, 42.0 mg) and cobalt nitrate hexahydrate (0.2 mmol, 58.2 mg) Dissolve in twice-distilled water (10.0 mL), adjust the pH to 3 with triethylamine, stir for several minutes, and seal it into a hydrothermal kettle. at 170 o After incubation at C for 4 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
[0032] Synthesis of 5-methyl-1H-tetrazolium and 1,2,3-trimesic acid mixed ligand cobalt(II) complex B:
[0033] 5-Methyl-1H-tetrazolium (0.2 mmol, 16.8 mg), 1,2,3-trimesic acid (0.2 mmol, 42.0 mg) and cobalt nitrate hexahydrate (0.3 mmol, 87.2 mg) Dissolve in twice-distilled water (10.0 mL), adjust the pH to 3 with triethylamine, stir for several minutes, and seal it into a hydrothermal kettle. at 180 o After incubation at C for 4 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. See figure 1 crystal structure diagram.
Embodiment 3
[0035] Synthesis of 5-methyl-1H-tetrazolium and 1,2,3-trimesic acid mixed ligand cobalt(II) complex C:
[0036] 5-Methyl-1H-tetrazolium (0.2 mmol, 16.8 mg), 1,2,3-trimesic acid (0.2 mmol, 42.0 mg) and cobalt nitrate hexahydrate (0.2 mmol, 58.2 mg) Dissolve in twice-distilled water (10.0 mL), adjust the pH to 3 with triethylamine, stir for several minutes, and seal it into a hydrothermal kettle. at 185 o After incubation at C for 4 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. See figure 1 crystal structure diagram.
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