Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Azaxanthone compound and applications of azaxanthone compound in OLED light emitting devices

A technology of xanthone and compound, applied in the direction of electric solid device, semiconductor device, chemical instrument and method, can solve the problems of limited application, lower triplet energy level, etc., achieve good optoelectronic performance, increase orbital overlap, Avoid the effect of agglomeration

Active Publication Date: 2017-10-13
JIANGSU SUNERA TECH CO LTD
View PDF8 Cites 23 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At the same time, there is a strong intramolecular charge transfer between the donor and the acceptor of the host material, which leads to the lowering of the triplet energy level of the material itself, which limits its application in industrial production.

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
  • Azaxanthone compound and applications of azaxanthone compound in OLED light emitting devices
  • Azaxanthone compound and applications of azaxanthone compound in OLED light emitting devices
  • Azaxanthone compound and applications of azaxanthone compound in OLED light emitting devices

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0050] Embodiment 1: the synthesis of R structure (shown in general formula 3)

[0051]

[0052] The preparation method of R structure (shown in general formula 3):

[0053] Weigh raw material I o-bromonitro compound, raw material II boric acid, and dissolve it in a mixed solvent of toluene and ethanol with a volume ratio of 2:1, and add potassium carbonate aqueous solution, Pd(PPh 3 ) 4 , reacted at 95-110°C for 10-24 hours, cooled to and filtered the reaction solution, the filtrate was rotary evaporated, and passed through a silica gel column to obtain the target product; the molar ratio of o-bromonitro compound to boric acid was 1:1.0~3.0; o-bromo The molar ratio of nitro compound to potassium carbonate is 1:1.0~3.0; o-bromonitro compound and Pd(PPh 3 ) 4 The molar ratio is 1:0.006~0.02;

[0054] Weigh the product from the previous step, dissolve it with o-dichlorobenzene, and then add PPh 3 , under an inert atmosphere, react the mixed solution of the above reactant...

Embodiment 2

[0061] Embodiment 2: the synthesis of R structure (shown in general formula 2)

[0062]

[0063] The preparation method of Reaction Formula 3-1 is: Weigh the corresponding raw material 1-o-aminophenol, raw material 2-o-nitrophenol, and iodine, stir and dissolve them with diethylene glycol as a solvent, and heat to 250-270°C under an inert atmosphere to react 12 -24 hours, take a sample point plate, after the reaction is over, naturally cool to room temperature, there is solid precipitation, filter, take the filter cake and pass through the neutral silica gel column to obtain the intermediate En; the mole of the o-nitrophenol and o-aminophenol The ratio is 1:0.8~2.0; the molar ratio of the o-nitrophenol and iodine is 1:0.05~0.1;

[0064] The preparation method of reaction formula 3-2 is: weigh the corresponding bromide and arylamine with methyl formate, then add Pd 2 (dba) 3 , tri-tert-butylphosphine, sodium tert-butoxide; under an inert atmosphere, react the mixed solutio...

Embodiment 3

[0075] Embodiment 3: the synthesis of compound 1

[0076]

[0077] In a 250ml four-necked flask, add 0.01mol 3-bromo-6-iodo-9-oxa-1-aza-anthracene-10-one, 0.030mol carbazole, 0.03mol tert-butyl Sodium alkoxide, 1 x 10 -4 mol Pd 2 (dba) 3 , 1×10 -4 mol of tri-tert-butylphosphine, 150ml of toluene, heated to reflux for 24 hours, sampling plate, reaction complete, natural cooling, filtration, filtrate rotary evaporation, silica gel column to obtain the target product with a purity of 99.12% and a yield of 63.80%. HRMS(m / z): [M+H] + , the theoretical value is 528.1712, and the measured value is 528.1703.

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
thicknessaaaaaaaaaa
thicknessaaaaaaaaaa
thicknessaaaaaaaaaa
Login to View More

Abstract

The invention discloses an azaxanthone compound and applications of the azaxanthone compound in organic electroluminescent devices. According to the present invention, the azaxanthone compound uses azaxanthone as the core, the molecules are not easily crystallized and are not easily aggregated, and the azaxanthone compound has good film forming property; and with the application of the azaxanthone compound as the light emitting layer main material of the OLED light emitting device, the current efficiency, the power efficiency and the external quantum efficiency of the device are greatly improved, and the service life of the device can be remarkably improved.

Description

technical field [0001] The invention relates to the technical field of semiconductors, in particular to an azaxanthone compound and its application as a host material of a light-emitting layer in an organic light-emitting diode. Background technique [0002] Organic electroluminescent (OLED: Organic Light Emission Diodes) device technology can be used to manufacture new display products and also can be used to make new lighting products, which is expected to replace the existing liquid crystal display and fluorescent lighting, and has a wide application prospect. [0003] The OLED light-emitting device is like a sandwich structure, including electrode material film layers, and organic functional materials sandwiched between different electrode film layers. Various functional materials are superimposed on each other according to the application to form an OLED light-emitting device. As a current device, when a voltage is applied to the electrodes at both ends of the OLED ligh...

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): C07D491/052C07D519/00C09K11/06H01L51/50H01L51/54
CPCC09K11/06C07D491/052C07D519/00C09K2211/1033C09K2211/1011C09K2211/1007C09K2211/1014C09K2211/1029H10K85/636H10K85/633H10K85/654H10K85/6572H10K50/11
Inventor 徐凯李崇张小庆张兆超
Owner JIANGSU SUNERA TECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products