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, which can solve the problems of backwardness and rarely achieve the color purity of dark red and dark green light, and achieve high luminous efficiency and good energy transmission efficiency , The effect that the preparation process is easy to control
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Embodiment 1
[0067] Example 1: A red-light organic electrophosphorescent material iridium metal complex tris[3-(4',6'-dimethylphenyl)-4-phenylcinnoline-N,C 2 '] Iridium, as shown in the following structural formula:
[0068]
[0069] The preparation method of the above-mentioned red light organic electrophosphorescent material iridium metal complex comprises the following steps:
[0070] (1) Provide compound A and Grignard reagent B1 represented by the following structural formula respectively:
[0071]
[0072] (2) Synthesis of 1-phenyl-1-(2'-aminophenyl)-2-(2',4'-dimethylphenyl)ethanol
[0073]
[0074] Under nitrogen protection, 1.97g (10mmol) 2-aminobenzophenone (compound A) was dissolved in 60mL of anhydrous ether, and 1.10g (45.8mmol) magnesium particles, 6.73g (43.5mmol) 2 , Grignard reagent B1 solution prepared by 4-dimethylbenzyl chloride (compound D) and 30 mL of anhydrous ether; after the dropwise addition, reflux for 45 min, add excess methanol and ammonium nitrate t...
Embodiment 2
[0104] Example 2: A red-light organic electrophosphorescent material iridium metal complex tris[3-(5',6'-dimethylphenyl)-4-phenylcinnoline-N,C 2 '] Iridium, as shown in the following structural formula:
[0105]
[0106] The preparation method of the above-mentioned red light organic electrophosphorescent material iridium metal complex comprises the following steps:
[0107] (1) Provide compound A and Grignard reagent B2 represented by the following structural formula respectively:
[0108]
[0109] (2) Synthesis of 1-phenyl-1-(2'-aminophenyl)-2-(2',3'-dimethylphenyl)ethanol
[0110]
[0111] Under nitrogen protection, 1.97g (10mmol) 2-aminobenzophenone was dissolved in 60mL of anhydrous ether, and 1.06g (43.5mmol) magnesium particles, 6.73g (43.5mmol) 2,3-bis Grignard reagent B2 solution prepared by methylbenzyl chloride and 30mL anhydrous ether; reflux for 40min after the dropwise addition, add excess methanol and ammonium nitrate to quench the reaction, wash with...
Embodiment 3
[0140] Example 3: A red-light organic electrophosphorescent material iridium metal complex tris[3-(3',6'-dimethylphenyl)-4-phenylcinnoline-N,C 2 '] Iridium, as shown in the following structural formula:
[0141]
[0142] The preparation method of the above-mentioned red light organic electrophosphorescent material iridium metal complex comprises the following steps:
[0143] (1) Provide compound A and Grignard reagent B3 represented by the following structural formula respectively:
[0144]
[0145] (2) Synthesis of 1-phenyl-1-(2'-aminophenyl)-2-(2',5'-dimethylphenyl)ethanol
[0146]
[0147] Under nitrogen protection, 1.97g (10mmol) of 2-aminobenzophenone was dissolved in 60mL 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 methylbenzyl chloride and 30mL anhydrous ether; reflux for 50min after the dropwise addition, add excess methanol and ammonium nitrate to quench the reaction, ...
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