Rare earth (III)-transition (II) mixed metal fluorescence complex and preparing method and application thereof
A transition metal ion, mixed metal technology, applied in fluorescence/phosphorescence, organic chemistry methods, chemical instruments and methods, etc., can solve problems to be further studied, and achieve high yield, high fluorescence emission intensity, selectivity and sensitivity high effect
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Embodiment 1
[0027] 8-hydroxyquinoline as ligand {Dy 2 co 2} Synthesis of fluorescent complex A:
[0028] 8-Hydroxyquinoline (0.3 mmol, 43.5 mg), cobalt nitrate hexahydrate (0.2 mmol, 58.2 mg), and dysprosium nitrate hexahydrate (0.2 mmol, 91.3 mg) were dissolved in anhydrous methanol (15.0 mL) , with NaHCO 3 The pH of the reaction mixture was adjusted to 5 by the solid, and it was sealed in a hydrothermal kettle after stirring for several minutes. Water heating kettle at 120 o After three days of incubation at C, at 4.0°C·h –1 The temperature was lowered to room temperature by the rate program, and the red blocky crystals were obtained, which were then washed with anhydrous methanol and dried in air.
Embodiment 2
[0030] {Dy based on 8-hydroxyquinoline as a ligand 2 Ni 2} Synthesis of fluorescent complex B:
[0031] 8-Hydroxyquinoline (0.3 mmol, 43.5 mg), nickel nitrate hexahydrate (0.2 mmol, 58.2 mg), and dysprosium nitrate hexahydrate (0.2 mmol, 91.3 mg) were dissolved in anhydrous methanol (15.0 mL) , with NaHCO 3 The pH of the reaction mixture was adjusted to 5 by the solid, and after stirring for several minutes, it was sealed in a hydrothermal kettle. Water heating kettle at 140 o After 3 days of incubation at C, at 3.2°C·h –1 The rate program cooled down to room temperature to obtain green blocky crystals, which were then washed with anhydrous methanol and dried in air.
Embodiment 3
[0033] {Tb based on 8-hydroxyquinoline ligand 2 co 2} Synthesis of fluorescent complex C:
[0034] 8-Hydroxyquinoline (0.3 mmol, 43.5 mg), cobalt nitrate hexahydrate (0.2 mmol, 58.2 mg) and terbium nitrate hexahydrate (0.2 mmol, 90.6 mg) were dissolved in anhydrous methanol (15.0 mL), with NaHCO 3 The pH of the reaction mixture was adjusted to 6 by the solid, and it was sealed in a hydrothermal kettle after stirring for several minutes. Water heating kettle at 120 o After three days of incubation at C, at 4.0°C·h –1 The rate program cooled down to room temperature to obtain red blocky crystals, which were then washed with anhydrous methanol and dried in air.
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