A plurality of host materials and organic electroluminescent device comprising the same
A main material and unreplaced technology, which is applied in the direction of luminescent materials, organic chemistry, organic semiconductor devices, etc., can solve the problems such as the use of organic electroluminescent devices that have not been specifically disclosed, and achieve the effect of improving life characteristics and high luminous efficiency
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example 1
[0124] Example 1: Preparation of Compound H2-1
[0125]
[0126] In a flask, mix 2-chloro-5-phenylpyrimidine (2.7g, 14.2mmol) and 5-phenyl-5,7-dihydroindolo[2,3-b]carbazole (3.5g, 10.9 mmol) into palladium (II) acetate (Pd(OAc) 2 ) (0.11g, 0.5mmol), ligand (2-dicyclohexylphosphine-2',6'-dimethoxybiphenyl) (0.45g, 1.1mmol), NaOt-bu (2.8g, 27.3mmol) , and toluene (200 mL), and the mixture was refluxed at 140° C. for 4 hours. After the reaction was completed, distilled water was added to the reaction mixture, and the organic layer was extracted with dichloromethane. The remaining moisture of the organic layer was removed using magnesium sulfate, and the residue was dried. The residue was separated by column chromatography to obtain 3.2 g of Compound H2-1 (yield: 60.3%) (melting point: 231° C.).
[0127] Device Example 1: Production of OLEDs Comprising Multiple Host Materials According to the Disclosure
[0128] OLEDs according to the present disclosure were produced. ...
example 2
[0130] Device Example 2: Production of OLEDs Comprising Multiple Host Materials According to the Disclosure
[0131] OLEDs were produced in the same manner as in Device Example 1, except that Compound H1-33 and Compound H2-1 were used as the first and second hosts, respectively.
example 3
[0132] Device Example 3: Production of OLEDs Comprising Multiple Host Materials According to the Disclosure
[0133] OLEDs were produced in the same manner as in Device Example 1, except that Compound H1-3 and Compound H2-1 were used as the first and second hosts, respectively.
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