Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Red organic electroluminescent material and its preparation method and application

An electroluminescence, electromechanical technology, applied in luminescent materials, organic chemistry, chemical instruments and methods, etc., can solve the problems of backwardness and rarely achieve the color purity of dark red and dark green light, to reduce the direct effect, Improve electroluminescence performance and balance the effect of charge transport

Inactive Publication Date: 2014-08-06
OCEANS KING LIGHTING SCI&TECH CO LTD +2
View PDF6 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Generally speaking, the development of blue phosphorescent materials always lags behind red light and green light. In terms of color purity alone, blue phosphorescent materials have rarely been able to achieve the same level as deep red light and deep green light. color purity

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
  • Red organic electroluminescent material and its preparation method and application
  • Red organic electroluminescent material and its preparation method and application
  • Red organic electroluminescent material and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0038] The preparation method of the above-mentioned red light organic electroluminescent material comprises the following steps:

[0039] S1. Under the protection of inert gas (at least one of nitrogen and argon, the same below), the structural formula is Compound A (2,5-dibromopyridine) and the structural formula is Compound B (9,9-dimethyl-2-fluoreneboronic acid) was dissolved in tetrakis(triphenylphosphine) palladium (Pd(PPh 3 )4 ) or dichlorobis(triphenylphosphine) palladium (Pd(PPh 3 ) 2 Cl 2 ) in an organic solvent of catalyst and alkali, and then reflux the Suzuki coupling reaction at 63~120°C for 8~10h. After the reaction stops, the reaction solution is separated and purified to obtain the structural formula: Compound C (2-(9',9'-dimethylfluoren-2'yl)-5-bromopyridine); wherein, the molar ratio of compound A to compound B is 1:1.2; the molar ratio of catalyst to compound A Ratio is 0.05:1; The molar ratio of alkali and compound A is 10:3; Reaction formula is as...

Embodiment 1

[0065] Example 1: Complex bis[2-(9',9'-dimethylfluoren-2'-yl)-5-benzoylpyridine-N,C 2 Synthesis of '](acetylacetonate) iridium

[0066] (1) Synthesis of 2-(9',9'-dimethylfluoren-2'yl)-5-bromopyridine

[0067]

[0068] 0.71g (3.0mmol) 2,5-dibromopyridine, 0.86g (3.6mmol) 9,9-dimethyl-2-fluoreneboronic acid, 0.17g (0.15mmol) tetrakis (triphenylphosphine) palladium, 25mL toluene , 12.5mL of ethanol and 5mL of 2M sodium carbonate (10.0mmol) aqueous solution were refluxed at 120°C for 8h. After the reaction was cooled to room temperature, it was poured into an appropriate amount of distilled water and extracted with ethyl acetate. The organic phase was dried over anhydrous magnesium sulfate. Filter and evaporate the solvent to obtain the crude product. The crude product was purified by silica gel column chromatography using a mixture of ethyl acetate and n-hexane with a volume ratio of 1:3 as the eluent to obtain 0.68 g of a white solid with a yield of 64.7%.

[0069] Struc...

Embodiment 2

[0098] Example 2: Complex bis[2-(9',9'-dimethylfluoren-2'-yl)-5-(naphthalene-1'-formyl)pyridine-N,C 2 '](acetylacetonate) iridium synthesis

[0099] (1) The synthesis steps of 2-(9',9'-dimethylfluoren-2'-yl)-5-bromopyridine were the same as in Example 1, except that the Suzuki coupling reaction was refluxed at 80°C for 9 hours;

[0100] (2) Synthesis of 2-(9',9'-dimethylfluoren-2'-yl)-5-(naphthalene-1'-formyl)pyridine

[0101]

[0102] Under the protection of argon, 1.40g (4.0mmol) of 2-(9',9'-dimethylfluoren-2'-yl)-5-bromopyridine was dissolved in 20mL of freshly distilled ether, and the temperature of the reaction system was lowered under stirring. down to -78°C. 4 mL of 1.6 M n-butyllithium (6.4 mmol) n-hexane solution was added dropwise with a syringe, the addition was completed within 10 min, and stirring was continued at -78°C for 35 min. 1.20g (6.0mmol) of N,N-dimethyl-naphthalen-1'-ylformamide was dissolved in 20mL of freshly distilled ether, and added dropwise t...

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

No PUM Login to View More

Abstract

The invention belongs to the organic electroluminescent material, and discloses a red organic electroluminescent material and a preparation method and application thereof. The material has a general structural formula as follows, wherein R represents phenyl, naphthyl-1-yl or naphthyl-2-yl. The red organic electroluminescent phosphorescent material provided by the invention uses 2-(9',9'-dimethyl fluorene-2'-yl)-5-aryl formyl pyridine as a main structure of a ring metal ligand, and the introduction of phenyl, naphthyl-1-yl and naphthyl -2-yl formyl realizes acquisition of satisfactory red emission wavelength; the presence of large groups such as triphenylamine, phenyl or naphthyl can produce a certain space steric effect, thereby reducing the direct interaction between metal atoms, and reducing self quenching phenomenon of triplet exciton; at the same time, aromatic groups can effectively control the energy levels of highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of the material, and facilitate the balance of charge transfer in a device, so as to improve the luminescent properties of the device.

Description

technical field [0001] The invention relates to an organic electroluminescent material, in particular to a red light organic electroluminescent material and a preparation method and application thereof. Background technique [0002] Organic electroluminescence refers to a luminescence phenomenon in which organic materials directly convert electrical energy into light energy under the action of an electric field. In the early days, the research on organic electroluminescence was stagnant because of the high driving voltage and low luminous efficiency of organic electroluminescent devices. Until 1987, people such as Tang of American Kodak Company invented 8-hydroxyquinoline aluminum (Alq 3 ) is a light-emitting material, and a uniform and dense high-quality thin film is made with aromatic diamines, and an organic electroluminescent device with low operating voltage, high brightness, and high efficiency is prepared, which opens a new prelude to the research on organic electrol...

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): C09K11/06C07F15/00H01L51/54
Inventor 周明杰王平张娟娟张振华
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
Eureka Blog
Learn More
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com