Organic compound and organic electroluminescent element comprising same
A compound and bonding technology, which is applied in the field of organic electroluminescent elements, can solve the problems of color purity and efficiency reduction of organic electric elements, charge imbalance of light-emitting layer, low HOMO value, etc., and achieve improved luminous efficiency and life characteristics, long-term Excellent life characteristics and low driving voltage
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Synthetic example 1-1
[0212]
[0213] 1-A) Synthesis of Intermediate 1-A
[0214]
[0215] 1-(4'-Bromo-[1,1'-biphenyl]-4-yl)adamantane (1-(4'-bromo-[1,1'-biphenyl ]-4-yl)adamantane, 100.0g, 272.2mmol), [1,1'-biphenyl]-4-amine ([1,1'-biphenyl]-4-amine, 50.68g, 299.5mmol), Pd 2 (dba) 3 (4.99g, 5.44mmol), t-BuONa (52.33g, 544.5mmol), 50% t-Bu 3 P solution (5.12mL, 21.78mmol) and toluene (1500mL) were stirred at 100°C to react. After the reaction was completed, methanol was added to precipitate, and the resulting solid was filtered, and then purified by silicagel column chromatography and recrystallization to prepare 100.5 g of compound 1-A (yield: 81%).
[0216] 1-B) Synthesis of compound 337
[0217]
[0218] Under nitrogen stream, add compound 1-A (10g, 21.95mmol), 3-bromodibenzofuran (3-bromodibenzofuran) (5.97g, 24.14mmol), Pd 2 (dba) 3 (0.40g, 0.44mmol), t-BuONa (4.22g, 43.89mmol), 50% t-Bu 3 P solution (0.41mL, 1.76mmol) and toluene (150mL) were stirred at 100°C to react. After t...
Synthetic example 1-2
[0219]
[0220]
[0221] Except that 2-bromodibenzofuran (2-bromodibenzofuran) (5.97g, 24.14mmol) was used instead of 3-bromodibenzofuran, the same method as that of compound 337 was used to synthesize and purify, and 8.46 g of compound 340 (yield: 62%).
Synthetic example 1-3
[0222]
[0223]
[0224] Except that 3-bromodibenzothiophene (3-bromodibenzothiophene, 6.35g, 24.14mmol) was used instead of 3-bromodibenzofuran, the synthesis and purification were carried out in the same way as that of compound 337, and 9.24g Compound 974 (yield: 66%).
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