Electroluminescent material of high efficiency rare-earth organic ligand and its preparing method
An electroluminescent material and rare earth technology, applied in luminescent materials, electroluminescent light sources, electric light sources, etc., can solve the problems of unsatisfactory device stability, cost reduction, few and other problems, and achieve excellent brightness and luminous spectrum stability. Effect
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Embodiment 1
[0025] Example 1 (DBM) 3 Preparation of Eu(bpyO):
[0026]
[0027] Dissolve DBM (dibenzoylacetone) (336.8mg, 1.5mmol) in ethanol (15ml), add 2M NaOH (0.75ml, 1.5mmol) and react at 50-60°C for 1 hour, then add EuCl 3 The aqueous solution (0.25mol / L, 2ml) was reacted at 50-60°C for 1 hour, and the obtained precipitate was filtered and washed with water and dissolved in tetrahydrofuran (15ml). mmol) was dissolved in tetrahydrofuran (3ml) and added to the above solution, and refluxed at 50-60°C for 4 hours. The solution was evaporated to dryness and washed with ethanol to obtain a powder product.
Embodiment 2
[0028] Example 2 (TTA) 3 Preparation of Eu(bpyO):
[0029]
[0030] Dissolve TTA (trifluoroacetylthiophene acetone) (333.3mg, 1.5mmol) in ethanol (15ml), add 2M NaOH (0.75ml, 1.5mmol) and react at 60-75°C for 1 hour, then add EuCl 3 Aqueous solution (0.25mol / L, 2ml), reacted at 60-75°C for 1 hour, dissolved monooxy-2,2'-bipyridine (86.1mg, 0.5mmol) in ethanol (3ml) and added to the reaction system After refluxing at 50-75°C for 30 minutes, a precipitate was obtained. The precipitate was washed with water and ethanol, and then recrystallized to obtain a single crystal.
Embodiment 3
[0031] Example 3 (DBM) 3 Preparation of Er(bpy0):
[0032]
[0033] Dissolve DBM (336.8mg, 1.5mmol) in ethanol (15ml), add 2M NaOH (0.75ml, 1.5mmol) and react at 50-65°C for 1 hour, then add ErCl 3 The aqueous solution (0.25mol / L, 2mol) was reacted at 55-65°C for 1 hour, and the obtained precipitate was filtered and washed with water. In tetrahydrofuran, monooxygenated-2,2'-bipyridine (86.1mg, 0.5mmol) was dissolved in Tetrahydrofuran was then added to the above solution and refluxed at 50-65°C for 4 hours. The solution was evaporated to dryness and washed with ethanol to obtain a powdery product.
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