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

Spiro ring organic photoelectric material, preparation method and applications thereof

A technology of organic photoelectric materials and spiro rings, which is applied in the preparation of organic compounds, luminescent materials, and hydrocarbon production from halogen-containing organic compounds, etc., can solve different problems and achieve avoidance of compact accumulation, high thermal stability, and high glass transition The effect of temperature

Active Publication Date: 2017-04-26
VALIANT CO LTD
View PDF4 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In addition, for OLEDs with different structures, the photoelectric functional materials used have strong selectivity, and the performance of the same material in OLEDs with different structures may be completely different.

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
  • Spiro ring organic photoelectric material, preparation method and applications thereof
  • Spiro ring organic photoelectric material, preparation method and applications thereof
  • Spiro ring organic photoelectric material, preparation method and applications thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0104] Embodiment 1. Preparation of organic optoelectronic materials

Embodiment 1

[0105] Example 1 Preparation of aforementioned compound 1

[0106] (1) Preparation of compound 1-a:

[0107]

[0108] At -15°C and under the protection of nitrogen, 23.1g of 2-bromo-4-hydroxybenzoic acid methyl ester (100.0mmol) and 121.4g (120mmol) of triethylamine were dispersed in 200g of dichloroethane, then drop Add 31.0 g of trifluoromethanesulfonic anhydride (110 mmol), after the dropwise addition, keep warm for 2.0 hours, then slowly warm up the reaction system to room temperature, then pour the above system into 200 g of water, stir and react for 30 min, the system is layered, and water is used to carry out the reaction. After washing, the organic phase was finally desolvated under reduced pressure until there was no fraction, and 36.1 g of compound 1-a was obtained without further purification.

[0109] (2) Preparation of compound 1-b:

[0110]

[0111] Get the 36.1g compound 1-a (100.0mmol), 20.7g potassium carbonate (150mmol), 80g water, 11.0g phenylboron...

Embodiment 2

[0133] Example 2 Preparation of aforementioned compound 8

[0134] (1) Preparation of compound 8-a:

[0135]

[0136] Take the 36.1g compound 1-a (100.0mmol), 20.7g potassium carbonate (150mmol), 80g water, 22.3g phenylboronic acid (90mmol) and 300g toluene obtained in step (1), under the protection of nitrogen, add catalyst 0.9 g Pd(PPh 3 ) 4 (0.75mmol), then heated to reflux, while adopting thin-layer chromatography (TLC) to track the reaction process, after about 6.0 hours of reaction, after being down to room temperature, the system was layered, and then after washing with water, the organic phase was decompressed and decompressed. Solvent until there is no fraction, and then use petroleum ether ethyl acetate mixture to carry out column chromatography purification to the residue, wherein the volume ratio of petroleum ether and ethyl acetate is petroleum ether:ethyl acetate=25:1, to obtain 22.5g of compound 8- a, The yield is 59.84%.

[0137] (2) Preparation of com...

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 present invention relates to a spiro ring organic photoelectric material and a preparation method thereof, and an organic electroluminescent device containing the spiro ring organic photoelectric material. According to the present invention, the provided organic electroluminescent device contains the spiro ring organic photoelectric material, such that the quantum efficiency, the current efficiency, the power efficiency and the brightness of the organic electroluminescent device can be substantially improved while the driving voltage is substantially reduced so as to significantly improve the service life of the organic electroluminescent device.

Description

technical field [0001] The invention relates to the field of optoelectronic technology, in particular to a spiro-ring organic optoelectronic material, its preparation method and its application. Background technique [0002] The origin of organic light emitting diode (OLED) can be traced back to the 1960s. Pope et al. used an anthracene single crystal to apply DC voltage to make it emit light, but due to the high driving voltage (100V) Moreover, the luminous brightness and efficiency are relatively low, which has not attracted too much attention. With the continuous improvement of technology. In 1987, C.W.Tang et al. of Kodak Company used 8-hydroxyquinoline aluminum (Alq3) as the luminescent material, and used the method of vacuum evaporation to make an OLED with a double-layer sandwich structure. The voltage is only a few volts, and the brightness can reach up to 1000cd / m 2 , thus marking an important step toward practical use of OLEDs, thus becoming an important mileston...

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): C07C1/26C07C13/72C07C17/263C07C25/22C07C253/30C07C255/52C07D307/91C07D307/77C07D409/10C07D209/86C07D213/127C07D213/16C07D333/76C09K11/06H01L51/50H01L51/54
CPCC09K11/06C07C13/72C07C25/22C07C255/52C07D209/86C07D213/127C07D213/16C07D307/77C07D307/91C07D333/76C07D409/10C09K2211/1092C09K2211/1088C09K2211/1011C09K2211/1029H10K85/624H10K85/626H10K85/6576H10K85/6574H10K85/6572H10K50/11
Inventor 张善国葛立权耿崴林存生付文岗胡葆华
Owner VALIANT 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