A red phosphorescent organic electroluminescent device
A red phosphorescence and luminescence technology, which is applied in the direction of electric solid-state devices, electrical components, semiconductor devices, etc., can solve the problem of low oxidation stability of the host material, improve the utilization rate of excitons, improve the efficiency and life, and reduce the triplet state -Effect of triplet annihilation
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Embodiment 1
[0066] Synthesis of compounds of structure shown in formula (1-1): under nitrogen range, 3,6-dibromo-9-fluorenone (5mmol), phenoxazine (18mmol), Pd 2 (dba) 3 (0.8mmol), NaOtBu (30mmol) and tBu 3 P·HBF 4 (0.8 mmol) was put into 100 mL of toluene and stirred overnight at a temperature of 105°C. The reaction was quenched by adding 10 mL of cold water to the mixture. After the mixture was cooled to room temperature, it was vacuum filtered, followed by purification by column chromatography to obtain the product with the structure shown in formula (1-1), and the product was dried in vacuum. Yield: 80%.
[0067] The molecular weight obtained by mass spectrometry: 542.58.
[0068] The relative molecular mass percentages of each element obtained by elemental analysis: C: 81.90%; H: 4.09%; N: 5.16%; O: 8.85%.
Embodiment 2
[0070] Synthetic compound of structure shown in formula (1-2): reactant phenoxazine is replaced by phenothiazine, through the same synthetic method as Synthetic Example 1, the compound of structure shown in formula (1-2) is obtained, productive rate 91% .
[0071] The molecular weight obtained by mass spectrometry: 574.71.
[0072] The relative molecular mass percentages of each element obtained by elemental analysis: C: 77.32%; H: 3.86%; N: 4.87%; O: 2.78%; S, 11.16%.
Embodiment 3
[0074] Synthetic compound of structure shown in formula (1-3): the reactant phenoxazine is replaced by 9,9-dimethylacridine, through the same synthetic method as in Synthesis Example 1, the structure shown in formula (1-3) is obtained Compound, yield 87%.
[0075] The molecular weight obtained by mass spectrometry: 594.74.
[0076] The relative molecular mass percentages of each element obtained by elemental analysis: C: 86.84%; H: 5.76%; N: 4.71%; O: 2.69%.
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