Mixed valence copper (I/II) complex containing a mixed ligand as well as preparation method and application thereof
A technology for mixing ligands and complexes, applied in the field of metals and metals, can solve the problems of limited research and few paramagnetic compounds, and achieve the effects of good reproducibility, high thermal stability and high yield
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Embodiment 1
[0026] Synthesis of 1,2,4-triazole and 5-nitroisophthalic acid mixed ligand mixed-valent copper complex A:
[0027] 1,2,4-Triazole (0.3 mmol, 21.0 mg), 5-nitroisophthalic acid (0.1 mmol, 21.0 mg) and copper nitrate trihydrate (0.1 mmol, 24.0 mg) were dissolved in di In sub-distilled water (10.0 mL), adjust the pH to 4 with triethylamine, stir for several minutes, and seal it into a hydrothermal kettle. at 160 o After incubation at C for 3 days, the temperature was programmed to cool down to room temperature to obtain a blue bulky single crystal, which was then washed with ethanol and dried in air. See figure 1 crystal structure diagram.
Embodiment 2
[0029] Synthesis of 1,2,4-triazole and 5-nitroisophthalic acid mixed ligand mixed-valent copper complex B:
[0030] 1,2,4-Triazole (0.3 mmol, 21.0 mg), 5-nitroisophthalic acid (0.1 mmol, 21.0 mg) and copper nitrate trihydrate (0.15 mmol, 36.0 mg) were dissolved in di In sub-distilled water (10.0 mL), adjust the pH to 4 with triethylamine, stir for several minutes, and seal it into a hydrothermal kettle. at 160 oC After 3 days of incubation, the temperature was lowered to room temperature to obtain a blue blocky single crystal, which was then washed with ethanol and dried. See figure 1 crystal structure diagram.
Embodiment 3
[0032] Synthesis of 1,2,4-triazole and 5-nitroisophthalic acid mixed ligand mixed-valent copper complex C:
[0033] 1,2,4-Triazole (0.3 mmol, 21.0 mg), 5-nitroisophthalic acid (0.1 mmol, 21.0 mg) and copper nitrate trihydrate (0.1 mmol, 24.0 mg) were dissolved in di In sub-distilled water (10.0 mL), adjust the pH to 4 with triethylamine, stir for several minutes, and seal it into a hydrothermal kettle. at 165 oC After 3 days of incubation, the temperature was lowered to room temperature to obtain a blue blocky single crystal, which was then washed with ethanol and dried. See figure 1 crystal structure diagram.
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