Organic compound and organic electroluminescent device comprising same
A technology of compounds and chemical formulas, applied in the field of organic electroluminescent elements, can solve the problems of unsatisfactory lifespan of light-emitting elements, poor thermal stability, low glass transition temperature, etc.
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Synthetic example 1
[0311] [Synthesis Example 1] Synthesis of R1
[0312]
[0313] Under nitrogen flow, 6.8 g (17.1 mmol) of A1, 8.7 g (18.8 mmol) of 2-(3'-bromobiphenyl-3-yl)-4,6-diphenyl-1,3,5 - Triazine, 1.0g (5mol%) of Pd (PPh 3 ) 4 , and 7.1g (51.2mmol) of potassium carbonate and 80ml / 40ml / 40ml of toluene / H 2 O / ethanol, stirred at 110°C for 3 hours.
[0314] After the reaction, the organic layer was separated using dichloromethane, and MgSO 4 The water is removed. After removing the solvent of the organic layer, the target compound R1 (8.4 g, 12.8 mmol, yield 75%) was obtained by column chromatography purification.
[0315] GC-Mass (theoretical value: 653.8g / mol, measured value: 653g / mol)
Synthetic example 2R8
[0316] [Synthesis Example 2] Synthesis of R8
[0317]
[0318] Under a stream of nitrogen, 6.8 g (17.1 mmol) of A1, 9.2 g (18.8 mmol) of 2-bromo-4,6-bis(dibenzo[b,d]furan-4-yl)-1,3 , 5-triazine, 1.0g (5mol%) of Pd (PPh 3 ) 4 And 7.1g (51.2mmol) of potassium carbonate and 80ml / 40ml / 40ml of toluene / H 2 O / ethanol, stirred at 110°C for 3 hours.
[0319] After the reaction, the organic layer was separated using dichloromethane, and MgSO 4 The water is removed. After removing the solvent of the organic layer, it purified by column chromatography to obtain the target compound R8 (9.0 g, 13.1 mmol, yield 77%).
[0320] GC-Mass (theoretical value: 681.8g / mol, measured value: 682g / mol)
Synthetic example 3R21
[0321] [Synthesis Example 3] Synthesis of R21
[0322]
[0323] Under a nitrogen stream, 6.8 g (17.1 mmol) of A2, 8.7 g (18.8 mmol) of 2-(3'-bromobiphenyl-3-yl)-4,6-diphenyl-1,3,5 - Triazine, 1.0g (5mol%) of Pd (PPh 3 ) 4 , and 7.1g (51.2mmol) of potassium carbonate and 80ml / 40ml / 40ml of toluene / H 2 O / ethanol, stirred at 110°C for 3 hours.
[0324] After the reaction, the organic layer was separated using dichloromethane, and MgSO 4 The water is removed. After removing the solvent of the organic layer, the target compound R21 (7.8 g, 11.9 mmol, yield 70%) was obtained by column chromatography purification.
[0325] GC-Mass (theoretical value: 654.8g / mol, measured value: 655g / mol)
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