Organic Electroluminescent Materials and Devices
An organic layer and electrode technology, applied in the application of organic electroluminescent devices, in the field of compounds containing quinazolinotriazole, an electron-deficient group structure, can solve the problem of reducing the recombination probability of holes and electrons, reducing The luminous efficiency of the device, the increase of the operating voltage of the device, etc., achieve the effects of good electron injection and transmission performance, improved device efficiency, and low driving voltage
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[0058] Preparation of compound 1-1
[0059] After 2,4-dichloroquinazoline (500g, 2.5mol) was dissolved in 10L ethanol in a flask, hydrazine hydrate (470g, 7.5mol, 80% aqueous solution) was added dropwise at 5°C under stirring, and the dropwise addition process kept the temperature low at 10°C. After the dropwise addition, the mixture was naturally raised to room temperature for 1 hour, and the precipitated solid was filtered with suction, washed with water and ethanol, and dried in the air to obtain compound 1-1 (415 g, 86%) as an off-white solid.
[0060] Preparation of compound 1-2
[0061] Compound 1-1 (200 g, 1.03 mol) was added to a flask containing 2 L of ethanol, and p-chlorobenzaldehyde (158 g, 1.13 mol) was added dropwise with stirring at room temperature. Stirring was continued for 30 minutes after the addition was complete, and TLC showed that the reaction was complete. Under stirring at room temperature, 1 L of ethanol solution in which iodobenzene acetate (364 g...
Embodiment 1
[0136] Using the compound C7 of the present invention as the electron transport material, an organic electroluminescent device was prepared according to the above-mentioned preparation process of the organic electroluminescent device, and the device performance was tested according to the above-mentioned organic electroluminescent device testing method.
Embodiment 2
[0138] An organic electroluminescent device was prepared by the same method as in Example 1, except that the compound C7 was replaced by C15.
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