Red organic electrophosphorescent material iridium metal complex, preparation method thereof, and organic electroluminescent device
A technology of iridium metal complexes and phosphorescent materials, applied in the field of organic electroluminescence, can solve the problems of rarely achieving deep red and dark green color purity, backwardness, etc., and achieve good energy transmission efficiency and high luminous efficiency , The effect of low processing cost
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Embodiment 1
[0071] Example 1: A red-light organic electrophosphorescent material iridium metal complex bis[3-(4',6'-dimethylphenyl)-4-phenylcinnoline-N,C 2 '](2,2,6,6-tetramethyl-3,5-heptanedione) iridium, as shown in the following structural formula:
[0072]
[0073] The preparation method of the above-mentioned red light organic electrophosphorescent material iridium metal complex comprises the following steps:
[0074] (1) Provide compound A and Grignard reagent B1 represented by the following structural formula respectively:
[0075]
[0076] (2) Synthesis of 1-phenyl-1-(2'-aminophenyl)-2-(2',4'-dimethylphenyl)ethanol
[0077]
[0078] Under the protection of nitrogen, 1.97g (10mmol) 2-aminobenzophenone (compound A) was dissolved in 60mL of anhydrous ether, and 1.06g (43.5mmol) magnesium particles, 6.73g (43.5mmol) 2 , Grignard reagent B1 solution prepared by 4-dimethylbenzyl chloride (compound D1) and 30 mL of anhydrous ether; after the dropwise addition, reflux for 40 mi...
Embodiment 2
[0108] Example 2: A red-light organic electrophosphorescent material iridium metal complex bis[3-(5',6'-dimethylphenyl)-4-phenylcinnoline-N,C 2 '](2,2,6,6-tetramethyl-3,5-heptanedione) iridium, as shown in the following structural formula:
[0109]
[0110] The preparation method of the above-mentioned red light organic electrophosphorescent material iridium metal complex comprises the following steps:
[0111] (1) Provide compound A and Grignard reagent B2 represented by the following structural formula respectively:
[0112]
[0113] (2) Synthesis of 1-phenyl-1-(2'-aminophenyl)-2-(2',3'-dimethylphenyl)ethanol
[0114]
[0115] Under nitrogen protection, 1.97g (10mmol) of 2-aminobenzophenone was dissolved in 50mL of anhydrous ether, and 1.16g (47.85mmol) of magnesium particles, 6.73g (43.5mmol) of 2,3-bis Grignard reagent B2 solution prepared by methylbenzyl chloride and 30mL anhydrous ether; reflux for 45min after the dropwise addition, add excess methanol and amm...
Embodiment 3
[0144] Example 3: A red-light organic electrophosphorescent material iridium metal complex bis[3-(3',6'-dimethylphenyl)-4-phenylcinnoline-N,C 2 '](2,2,6,6-tetramethyl-3,5-heptanedione) iridium, as shown in the following structural formula:
[0145]
[0146] The preparation method of the above-mentioned red light organic electrophosphorescent material iridium metal complex comprises the following steps:
[0147] (1) Provide compound A and Grignard reagent B3 represented by the following structural formula respectively:
[0148]
[0149] (2) Synthesis of 1-phenyl-1-(2'-aminophenyl)-2-(2',5'-dimethylphenyl)ethanol
[0150]
[0151] Under nitrogen protection, 1.97g (10mmol) of 2-aminobenzophenone was dissolved in 40mL of anhydrous ether, and 1.10g (45.8mmol) of magnesium particles, 6.73g (43.5mmol) of 2,5-bis Grignard reagent B3 solution prepared by methyl benzyl chloride and 30 mL of anhydrous ether; reflux for 45 minutes after the dropwise addition, add excess methano...
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