Organic electroluminescence material and application thereof

An organic compound and selected technology, applied in the fields of luminescent materials, organic chemistry, circuits, etc., can solve the problems of lower product cost, expensive materials, and efficiency roll-off, etc., and achieve device life improvement, reduce energy quenching, and efficiency roll-off. reduced effect

Inactive Publication Date: 2020-02-07
BEIJING ETERNAL MATERIAL TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the T1 lifetime of phosphorescent materials is generally above 1 μs, which is much higher than the lifetime of fluorescent materials of tens of nanoseconds, so the efficie

Method used

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  • Organic electroluminescence material and application thereof
  • Organic electroluminescence material and application thereof
  • Organic electroluminescence material and application thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0054] Preparation of intermediate M1:

[0055] Under the protection of nitrogen, add 400ml pivalic acid to a 1000ml single-necked flask and heat it to 50℃. Add bis(4-isopropyl)aniline (40g, 0.158mol), palladium acetate (35.6g, 0.158mol), carbonic acid at 50℃. Potassium (21.8g, 0.158mol), warm up to 100 degrees Celsius and react overnight. After the reaction is complete, extract with dichloromethane. Add 1000ml of saturated potassium carbonate to dichloromethane and stir well for 3 hours. After separation, filter with suction and reuse the organic phase. Wash once with 2000ml of saturated brine, spin dry, pass the silica gel through the column, spin dry the eluent, boil and wash with a small amount of petroleum ether to obtain 16g, the product, the yield is 40%, the purity is 99.9%, and it is off-white solid.

[0056] Preparation of compound C1:

[0057] Under the protection of nitrogen, add 3.1 g of sodium hydride to a 1000 ml three-necked flask, dissolve it in 50 ml of DMF, add 24...

Embodiment 1z

[0081] The obtained compounds are all prepared by sublimation purification process before device preparation, and the purification equipment is the company's EMT-50-X grade purification equipment. The specific operation process is as follows:

[0082] Take 1g of compound C7 and place it in a quartz boat, place the quartz boat in the purification equipment, and apply a vacuum to the equipment. When the vacuum degree is stable between 10-2~10-3Pa, set three temperature zones at 100℃ to turn on heating;

[0083] Gradually increase the temperature control, maintain an appropriate temperature difference between the high temperature zone, the medium temperature zone and the low temperature zone, observe the sublimation phenomenon, stop heating when a small amount of film is produced, and keep the temperature until the material sublimation is completed;

[0084] Open the furnace cover and wait for the temperature to drop to room temperature, turn off the pump, turn on the nitrogen, balance ...

Embodiment 1

[0114] The preparation process of organic electroluminescent device is as follows:

[0115] The glass plate coated with the transparent conductive layer of ITO is ultrasonically treated in a commercial cleaning agent, rinsed in deionized water, degreasing ultrasonically in a mixed solvent of acetone and ethanol, and baked in a clean environment until the water is completely removed. Light and ozone cleaning, and bombard the surface with low-energy cation beams;

[0116] Put the above-mentioned glass substrate with anode in the vacuum chamber and evacuate to 1×10 -5 ~9×10 -3 Pa, HI-2 was vacuum-evaporated on the above-mentioned anode layer film as a hole injection layer, the evaporation rate was 0.1 nm / s, and the evaporation film thickness was 10 nm;

[0117] Vacuum evaporate HT-2 on the hole injection layer as the hole transport layer of the device, the evaporation rate is 0.1nm / s, and the total evaporation film thickness is 40nm;

[0118] Vacuum evaporate HT-28 on the hole transport ...

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Abstract

The invention discloses an organic compound which has a structural formula as shown in a formula (1). In the formula (1), R1 is selected from CN, CF3 and NO2; m is an integer from 0 to 2, and n is aninteger from 2 to (5-m); Ar1 is selected from hydrogen, halogen, C1-C8 alkyl, C5-C10 cycloalkyl, C1-C8 alkoxy, C6-C14 aryl and C3-C12 heteroaryl, and multiple Ar1s can be the same or different; Ar2 has a structural formula as shown in a formula (2), and multiple Ar2s can be the same or different; in the formula (2), X is selected from single bonds, O, S, NR8 and CR9R10; * denotes the position of connection between the Ar2 and a benzene ring in the formula (1); each of R2-R7 is independently selected from hydrogen or C1-C14 electron donating group, and at least one is C3-C12 non-tertiary-carbonbranched alkyl; any two of the R2-R7 can form a ring; and each of R8-R10 is independently selected from hydrogen, halogen, carbonyl, C1-C8 alkyl, C5-C10 cycloalkyl, C1-C8 alkoxy, C6-C14 aryl and C3-C12 heteroaryl or a combination thereof.

Description

Technical field [0001] The present invention relates to an organic compound, which can be used as a light-emitting material of an organic electroluminescent device; the present invention also relates to the application of the compound in an organic electroluminescent device. Background technique [0002] Under electro-excitation conditions, organic electroluminescent materials will produce 25% singlet states and 75% triplet states. Traditional fluorescent materials can only use singlet excitons due to spin forbidden. In order to use triplet excitons, researchers have proposed many methods, the most notable of which is the use of phosphorescent materials. However, phosphorescent materials generally have a T1 lifetime of more than 1μs, which is much higher than the lifetime of fluorescent materials of tens of nanoseconds. Therefore, the efficiency roll-off is serious at high current densities, and the materials are more expensive due to the use of rare heavy metals, which is not co...

Claims

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Application Information

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IPC IPC(8): C07D209/86C07D265/38C07D279/22C07D219/02C07D401/14C07D241/46C09K11/06H01L51/50H01L51/54
CPCC07D209/86C07D265/38C07D279/22C07D219/02C07D401/14C07D241/46C09K11/06C09K2211/1007C09K2211/1029C09K2211/1033C09K2211/1037C09K2211/1044H10K85/654H10K85/657H10K85/6572H10K50/11H10K50/00
Inventor 高文正魏金贝邵爽
Owner BEIJING ETERNAL MATERIAL TECH
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