Organic light emitting compound and organic electroluminescent device using same
A compound and chemical formula technology, applied in the field of organic electroluminescent elements, can solve the problems of low glass transition temperature, low triplet energy, poor thermal stability, etc., and achieve the effect of excellent luminescence ability and improved efficiency
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Synthetic example 1
[0197] [Synthesis Example 1] Synthesis of Compound 1
[0198]
[0199] Mix PPY-1 3.0g with (9,9-dimethyl-9H-fluoren-2-yl) boronic acid 4.3g and K 2 CO 3 3.3 g was mixed, and after adding 60 ml of toluene, 12 ml of ethanol and 12 ml of water, 500 mg of tetrakistriphenylphosphine palladium (0) was added, followed by heating and stirring for 4 hours. After the reaction, the temperature was lowered to normal temperature, and then filtered. Pour the filtrate into water, extract with chloroform, use MgSO 4 The organic layer was dried. After concentration under reduced pressure, column chromatography was performed at MC:Hex=2:1 to obtain 2.8 g of compound 1 as a white solid (55% yield).
[0200] Quality: [(M+H) + ]:502
Synthetic example 2
[0201] [Synthesis Example 2] Synthesis of Compound 2
[0202]
[0203] Mix 3.0g of PPY-1 with 5.1g of 9,9'-spirobis[fluorene]-2-ylboronic acid and K 2 CO 3 3.3 g was mixed, and after adding 60 ml of toluene, 12 ml of ethanol and 12 ml of water, 500 mg of tetrakistriphenylphosphine palladium (0) was added, followed by heating and stirring for 4 hours. After the reaction, the temperature was lowered to normal temperature, and then filtered. Pour the filtrate into water, extract with chloroform, use MgSO 4 The organic layer was dried. After concentration under reduced pressure, column chromatography was performed at MC:Hex=2:1 to obtain 3.2 g of compound 2 as a white solid (58% yield).
[0204] Quality: [(M+H) + ]:624
Synthetic example 3
[0205] [Synthesis Example 3] Synthesis of Compound 4
[0206]
[0207] Mix PPY-1 3.1g with (7,7-dimethyl-7H-benzo[c]fluoren-9-yl)boronic acid 4.8g and K 2 CO 3 3.3 g was mixed, and after adding 60 ml of toluene, 12 ml of ethanol and 12 ml of water, 500 mg of tetrakistriphenylphosphine palladium (0) was added, followed by heating and stirring for 4 hours. After the reaction, the temperature was lowered to normal temperature, and then filtered. Pour the filtrate into water, extract with chloroform, use MgSO 4 The organic layer was dried. After concentration under reduced pressure, column chromatography was performed at MC:Hex=2:1 to obtain 3.5 g of compound 4 as a white solid (yield 56%).
[0208] Quality: [(M+H) + ]:551
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