Phenazine derivatives and their use in organic electroluminescent device
A technology of electroluminescent devices and derivatives, applied in the direction of electric solid devices, electrical components, organic chemistry, etc., can solve the problems of reducing OLED costs, disadvantages, and increasing the complexity of device manufacturing processes, so as to improve luminous efficiency and reduce work Effect of voltage, good ability to accept electrons
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Embodiment 1
[0049] The synthesis of embodiment 1 dibromophenazine
[0050]
[0051] Add 3.91 grams of 4-bromo-o-phenylenediamine (molecular weight 186, 0.021 mol), 3.91 grams of 4-bromo-o-benzoquinone (molecular weight 186, 0.021 mol), ethanol (40 ml) into a 250 ml three-necked flask, and stir for 3 minutes Add 0.2 gram of concentrated sulfuric acid (concentration 98%) dropwise, and react at 65°C for 4 hours. After the reaction, cool to room temperature, filter, wash with water, dry, separate by column chromatography, and rinse with ethyl acetate / petroleum ether to obtain Almost equal amounts of 2,7-dibromophenazine and 2,8-dibromophenazine totaled 5.82 g (molecular weight: 336), and the total yield was 82.4%.
Embodiment 2
[0053] Synthesis of compound shown in formula (4)
[0054]
[0055] 1000 ml three-necked flask equipped with magnetic stirring and nitrogen protection, add 6.72 g of 2,8-dibromophenazine (molecular weight 336, 0.02 mol), 7.4 g of naphthalene-2-boronic acid (molecular weight 172, 0.043 mol), tetrakis(triphenyl 2.3 g of palladium (molecular weight: 1154, 0.002 mol), 100 ml of 2M sodium carbonate aqueous solution, 100 ml of toluene, and 100 ml of ethanol. After argon replacement, the reaction was refluxed, and the reaction was monitored by thin-layer chromatography (TLC). After 3.5 hours, TLC found that the raw material bromide was completely reacted, and only the product point was present. The temperature was lowered, the organic layer was separated, evaporated to dryness, separated by column chromatography, and washed with ethyl acetate / petroleum ether to obtain 8.1 g of the compound represented by formula (4), with a molecular weight of 432 and a yield of 93.8%.
[0056] P...
Embodiment 3
[0058] Synthesis of compound shown in formula (5)
[0059] The synthesis steps are the same as in Example 2, except that naphthalene-2-boronic acid is changed to naphthalene-1-boronic acid, and other reagents remain unchanged to obtain the compound shown in formula (5).
[0060] Product MS (m / e): 432, elemental analysis (C 32 h 20 N 2 ): theoretical value C: 88.86%, H: 4.66%, N: 6.48%; measured value C: 88.88%, H: 4.67%, N: 6.45%.
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