Bipolar blue light phosphorescent host material, preparation method and organic electroluminescent device thereof

A phosphorescent main body and bipolar technology, which is applied in the manufacture of electric solid-state devices, semiconductor devices, semiconductor/solid-state devices, etc., can solve problems such as shortages, achieve reduced manufacturing costs, cheap and easy-to-obtain raw materials, and good thermal stability Effect

Inactive Publication Date: 2014-12-03
OCEANS KING LIGHTING SCI&TECH CO LTD +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patented BPBNP (bimodal yellow pigments) emits strong greenish colored lights when excited with ultraviolet rays or near infrared radiation. It also allows for efficient transferring of three different types of charges: positive charge carriers like oxygen atoms, negative ones such as sulfur dioxide molecules, into an organic matrix called quantum dots. These charged particles help balance up any excessive electric fields inside them while allowing more excitation levels from outside sources. By adjusting these parameters, this technology makes it possible to create high-quality displays without adding extra layers on top.

Problems solved by technology

This patents discusses different ways for improving the emission properties of organic EL displays by adding certain substances that help them perform better with electrons from their ground states during operation. These improvements include improved electron injection capabilities or increased triplets levels at other layers within an active layer.

Method used

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  • Bipolar blue light phosphorescent host material, preparation method and organic electroluminescent device thereof
  • Bipolar blue light phosphorescent host material, preparation method and organic electroluminescent device thereof
  • Bipolar blue light phosphorescent host material, preparation method and organic electroluminescent device thereof

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Experimental program
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Effect test

Embodiment 1

[0037] The bipolar blue phosphorescent host material of this embodiment has the structure: 9-(4-(3,5-diphenyl-4H-1,2,4-triazol-4-yl)benzene)-9H- Carbazole, the structural formula is as follows:

[0038]

[0039] The preparation process of the compound is as follows:

[0040]

[0041] Under the protection of nitrogen, 3,5-diphenyl-4H-1,2,4-triazole (17.7g, 80mmol) was dissolved in 200mL of N,N-dimethylformamide (DMF) solution, and then 9 -(4-Bromophenyl)-9H-carbazole (25.7g, 80mmol), potassium carbonate (22.1g, 160mmol), cuprous iodide (1.52g, 8mmol). The mixture was stirred and reacted at 120°C for 3 hours. The reaction was stopped, cooled to room temperature, filtered, and the solid was washed three times with distilled water. The crude product was separated by a silica gel chromatography column using eluent n-hexane, and then dried under vacuum at 50°C for 24 hours to obtain an off-white solid bipolar blue phosphorescent host material. The yield was 81%.

[0042] Mass spectrum: m

Embodiment 2

[0045] The bipolar blue phosphorescent host material of this embodiment is: 9-(4-(3,5-diphenyl-4H-1,2,4-triazol-4-yl)benzene)-9H-carbazole , The structural formula is as follows:

[0046]

[0047] The preparation process of the compound is as follows:

[0048]

[0049] Under the protection of nitrogen, 3,5-diphenyl-4H-1,2,4-triazole (17.7g, 80mmol) was dissolved in 200mL of toluene (Tol) solution, and then 9-(4-bromophenyl) was added )-9H-carbazole (28.2g, 88mmol), cesium carbonate (57.2g, 176mmol), copper powder (0.768g, 12mmol). The mixture was stirred and reacted at 110°C for 6 hours. The reaction was stopped, cooled to room temperature, filtered, and the solid was washed three times with distilled water. The crude product was separated by a silica gel chromatography column using eluent n-hexane, and then dried under vacuum at 50°C for 24 hours to obtain an off-white solid bipolar blue phosphorescent host material. The yield was 78%.

Embodiment 3

[0051] The bipolar blue phosphorescent host material of this embodiment is: 9-(4-(3,5-diphenyl-4H-1,2,4-triazol-4-yl)benzene)-9H-carbazole , The structural formula is as follows:

[0052]

[0053] The preparation process of the compound is as follows:

[0054]

[0055] Under the protection of nitrogen, 3,5-diphenyl-4H-1,2,4-triazole (17.7g, 80mmol) was dissolved in 200mL of acetonitrile (MeCN) solution, and then 9-(4-bromophenyl) )-9H-carbazole (30.8g, 96mmol), potassium phosphate (39g, 184mmol), cuprous oxide (2.3g, 16mmol). The mixture was stirred and reacted at 90°C for 8 hours. The reaction was stopped, cooled to room temperature, filtered, and the solid was washed three times with distilled water. The crude product was separated by a silica gel chromatography column using eluent n-hexane, and then dried under vacuum at 50°C for 24 hours to obtain an off-white solid bipolar blue phosphorescent host material. The yield was 74%.

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Abstract

The invention belongs to the field of organic semiconductor materials, and discloses a bipolar blue light phosphorescent host material, a preparation method and an organic electroluminescent device thereof. The host material has a structural formula shown as the specification. The bipolar blue light phosphorescent host material provided by the invention has hole transport properties and electron transport properties at the same time, and enables balance transport of holes and electrons in a luminescent layer. With a high triplet state energy level, the host material can effectively prevent back transmission of energy to the host material in a luminescence process, thus greatly improving the luminescence efficiency.

Description

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Claims

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Application Information

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Owner OCEANS KING LIGHTING SCI&TECH CO LTD
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