Red phosphorescence iridium complexes, preparing method thereof and organic electroluminescence device
A technology of iridium metal complex and red phosphorescence, applied in red phosphorescence iridium metal complex, its preparation, the field of organic electroluminescence devices, can solve the problems of low efficiency, difficult to obtain satisfactory luminescence performance and the like
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[0035] see figure 1 , the preparation method of the red phosphorescent iridium metal complex of an embodiment, comprises the steps:
[0036]Step S110: In the first inert gas atmosphere, dissolve 1-R-4-bromophthalazine and acenaphthylene-5-boronic acid in the first solvent with a molar ratio of 4:4.8~5, and add catalyst and carbonate solution , carry out Suzuki coupling reaction for 8 to 12 hours, and obtain ring metal main ligand 1-R-4-(acenaphthyl-5-yl)phthalazine after separation and purification.
[0037] Among them, -R in 1-R-4-bromophthalazine is the general formula -C n h 2n+1 Alkyl, the general formula is -OC n h 2n+1 alkoxy, phenyl or phenoxy, n is an integer of 1-20.
[0038] The general formula is -C n h 2n+1 The alkyl group is straight-chain or branched-chain. The general formula is -OC n h 2n+1 The alkoxy group is a straight chain alkoxy group or a branched chain alkoxy group.
[0039] The first inert gas is argon, helium or neon.
[0040] The first sol...
Embodiment 1
[0073] Red phosphorescent tris[1-methyl-4-(acenaphth-5-yl)phthalazine-N,C 2' ] Synthesis of iridium complexes.
[0074] Red phosphorescent tris[1-methyl-4-(acenaphth-5-yl)phthalazine-N,C 2' ] The structural formula of the iridium complex is as follows:
[0075]
[0076] (1) Synthesis of 1-methyl-4-(acenaphthyl-5-yl)phthalazine
[0077] In an argon atmosphere, 0.89 g (4 mmol) of 1-methyl-4-bromophthalazine, 0.95 g (4.8 mmol) of acenaphthylene-5-boronic acid and 0.23 g (0.20 mmol) of tetrakistriphenylphosphine palladium were dissolved in 30 mL 10 mL of an aqueous solution containing 0.85 g (8 mmol) of sodium carbonate was then added dropwise to the reaction system. Heated and stirred under reflux for 10h. After the reaction is complete, the reaction solution is naturally cooled to room temperature, extracted several times with an appropriate amount of water and ethyl acetate, the organic phase is dried with anhydrous magnesium sulfate, filtered, and the solvent in the fil...
Embodiment 2
[0109] Red phosphorescent tris[1-methoxy-4-(acenaphthyl-5-yl)phthalazine-N,C 2' ] Synthesis of iridium complexes.
[0110] Red phosphorescent tris[1-methoxy-4-(acenaphthyl-5-yl)phthalazine-N,C 2' ] The structural formula of the iridium complex is as follows:
[0111]
[0112] (1) Synthesis of 1-methoxy-4-(acenaphthyl-5-yl)phthalazine
[0113] In a neon atmosphere, dissolve 0.96g (4mmol) of 1-methoxy-4-bromophthalazine, 0.99g (5mmol) of acenaphthene-5-boronic acid and 0.28g (0.24mmol) of palladium tetrakistriphenylphosphine in 25mL In THF, 10 mL of an aqueous solution containing 1.38 g (10 mmol) of potassium carbonate was then added dropwise to the reaction system. Heated and stirred under reflux for 12h. After the reaction is complete, the reaction solution is naturally cooled to room temperature, extracted several times with an appropriate amount of water and ethyl acetate, the organic phase is dried with anhydrous magnesium sulfate, filtered, and the solvent in the fi...
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