Blue light organic electroluminescent material, preparation method and applications thereof

A luminescent and electromechanical technology, applied in luminescent materials, organic chemistry, chemical instruments and methods, etc., to achieve high fluorescence quantum yield, good thermal stability, and high device luminous efficiency

Inactive Publication Date: 2015-05-20
OCEANS KING LIGHTING SCI&TECH CO LTD +2
View PDF0 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although many blue light materials have been reported, there are still few materials with high efficiency and stable emission performance.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Blue light organic electroluminescent material, preparation method and applications thereof
  • Blue light organic electroluminescent material, preparation method and applications thereof
  • Blue light organic electroluminescent material, preparation method and applications thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] Example 1: The blue-light organic electroluminescent material of this example, that is, 10,10'-(benzo[k]fluoranthene-7,12-diyl)bis(N,N-diphenylanthracene-9- Amine), the preparation steps are as follows:

[0037]

[0038] Under the protection of argon, 7,12-dibromobenzo[k]fluoranthene (82mg, 0.2mmol), 10-(diphenylamine) anthracene-9-boronic acid (156mg, 0.4mmol) were added to a 10ml toluene In the flask of the solvent, after fully dissolving, potassium carbonate (2mL, 2mol / L) solution was added into the flask, vacuumed to remove oxygen and filled with argon, then added bistriphenylphosphine palladium dichloride (5.6mg, 0.008 mmol); the flask was heated to 120°C for Suzuki coupling reaction for 24h. The reaction was stopped and cooled to room temperature, the reaction solution was extracted with dichloromethane several times and the organic phase was combined. After the organic phase was dried over anhydrous magnesium sulfate and spin-dried, the crude product was obta...

Embodiment 2

[0040] Example 2: The blue-light organic electroluminescent material of this example has a structure of 10,10'-(benzo[k]fluoranthene-7,12-diyl)bis(N,N-diphenylanthracene- 9-amine), the preparation steps are as follows:

[0041]

[0042]Under the protection of mixed gas of nitrogen and argon, 7,12-dibromobenzo[k]fluoranthene (123mg, 0.3mmol), 10-(diphenylamine)anthracene-9-boronic acid (257mg, 0.66mmol) and Add 15mL tetrahydrofuran into a 50mL two-neck bottle, fully dissolve it, and then pass in a mixture of nitrogen and argon to exhaust the air for about 20 minutes, then add tetrakistriphenylphosphine palladium (4mg, 0.003mmol) into it, and then add it after fully dissolving Sodium bicarbonate (3mL, 2mol / L) solution. Then, the mixed gas of nitrogen and argon was exhausted for about 10 minutes, and the two-neck flask was added to 70°C for Suzuki coupling reaction for 48 hours. The reaction was stopped and cooled to room temperature, the reaction solution was extracted with...

Embodiment 3

[0043] Example 3: The blue-light organic electroluminescent material of this example has a structure of 10,10'-(benzo[k]fluoranthene-7,12-diyl)bis(N,N-diphenylanthracene- 9-amine), the preparation steps are as follows:

[0044]

[0045] Under nitrogen protection, 7,12-dibromobenzo[k]fluoranthene (123mg, 0.3mmol), 10-(diphenylamine)anthracene-9-boronic acid (280mg, 0.72mmol), palladium acetate (3.5mg ,0.015mmol) and tri(o-methylphenyl)phosphine (21mg, 0.06mmol) were added to a flask filled with 12mL of N,N-dimethylformamide, and potassium carbonate (3mL, 2mol / L) solution, followed by passing nitrogen into the flask to exhaust the air for about 30 minutes; heating the flask to 130° C. for Suzuki coupling reaction for 12 hours. The reaction was stopped and cooled to room temperature, the reaction solution was extracted with dichloromethane several times and the organic phase was combined. After the organic phase was dried over anhydrous magnesium sulfate and spin-dried, the ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
glass transition temperatureaaaaaaaaaa
Login to view more

Abstract

The invention belongs to the field of organic electroluminescent materials, and discloses a blue light organic electroluminescent material, a preparation method and applications thereof, wherein the structure formula of the material is defined in the instruction. According to the blue light organic electroluminescent material of the present invention, the luminescence is at the blue light region, the material has the high fluorescence quantum yield, and the luminous efficiency of the organic electroluminescent device adopting the material as the luminous layer material is high.

Description

technical field [0001] The invention relates to the field of organic electroluminescent materials, in particular to a blue-light organic electroluminescent material and its preparation method and application. Background technique [0002] Since the first report of organic light-emitting diodes (OLEDs) by C.W. Tang et al., both small-molecule and polymer-based LEDs, great progress has been made. Its potential applications are full-color flat-panel displays and solid-state white lighting. Among the three primary colors, red and green diodes are close to the requirements of practical applications, but blue materials have larger carrier injection due to their wider band gap and lower highest occupied orbital (HOMO) energy level. At the same time, due to the high emission energy, instability, and easy energy transfer, the emission color is impure, so the development is relatively slow. It is still a difficult problem to develop blue light emitting materials with high efficiency...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C09K11/06C07C211/61C07C209/68H01L51/54
Inventor 周明杰张振华王平钟铁涛
Owner OCEANS KING LIGHTING SCI&TECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap