A thermally activated delayed fluorescent material and an organic electroluminescent device
A technology of thermally activated delayed and fluorescent materials, applied in luminescent materials, electro-solid devices, organic chemistry, etc., can solve the problem of low efficiency of the luminescent layer, and achieve the effects of high radiation transition rate, good stability and short lifespan
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Embodiment 1
[0068] Synthetic method of the structural compound 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 tBu3P·HBF4 (0.8mmol) were put into 100mL toluene and stirred at 105°C overnight. 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 and then purified by column chromatography to obtain the product with the structure shown in formula (1-1). The product was dried in vacuum, yield: 80%.
[0069] The molecular weight obtained by mass spectrometry: 542.58.
[0070] 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
[0072] Synthetic method of the structural compound shown in formula (1-2): the reactant phenoxazine is replaced by phenothiazine, through the same synthetic method as in Example 1, the structural compound shown in formula (1-2) is obtained, and the yield is 91% .
[0073] The molecular weight obtained by mass spectrometry: 574.71.
[0074] 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
[0076] Synthesis method of the compound with the structure shown in formula (1-3): the reactant phenoxazine is replaced by 9,9-dimethylacridine, and the structure shown in formula (1-3) is obtained through the same synthesis method as in Example 1 Compound, yield 87%.
[0077] The molecular weight obtained by mass spectrometry: 594.74.
[0078] 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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