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Quinolone derivatives and application thereof in organic light-emitting devices (OLEDs)

A technology of organic groups and compounds, applied in the field of organic electroluminescent materials, can solve the problem of low fluorescence quantum efficiency and so on

Inactive Publication Date: 2011-05-25
TECHNICAL INST OF PHYSICS & CHEMISTRY - CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to the fact that the emission peak position of quinolone derivatives is biased towards the ultraviolet and the fluorescence quantum efficiency is not high, there has been no relevant report on using them as OLED host materials.

Method used

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  • Quinolone derivatives and application thereof in organic light-emitting devices (OLEDs)
  • Quinolone derivatives and application thereof in organic light-emitting devices (OLEDs)
  • Quinolone derivatives and application thereof in organic light-emitting devices (OLEDs)

Examples

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Effect test

Embodiment 1

[0075] Embodiment 1,1-methyl-3, the preparation of 4-diphenylquinolin-2 (1H)-ketone (Q1)

[0076]

[0077] The first step: take 1-methyl-4-phenylquinolin-2(1H)-one with a molar ratio of 1:1, and N-bromosuccinimide as raw materials, and dissolve the above-mentioned raw materials in N, N-dimethylformamide was reacted with stirring at room temperature for 10 hours, and a large amount of solid was precipitated by adding water, which was washed and dried to obtain the corresponding bromide with a yield of 80%.

[0078] The second step: under the protection of nitrogen, the bromide obtained in the first step and phenylboronic acid (molar ratio is 1: 1) are dropped into two-necked flasks, and a catalytic amount of tetrakis (triphenyl) phosphine palladium) and mixed solvent ( Sodium carbonate solution (2mol / L):toluene:ethanol=1:4:4), keep the temperature at 90-100°C, stir for 24 hours, extract with ether, and the product is subjected to column chromatography (eluent is petroleum et...

Embodiment 2

[0090] Embodiment 2, the preparation of 1-methyl-3-(2-naphthyl)-4-phenylquinolin-2(1H)-one (Q2)

[0091]

[0092] The first step: take 1-ethyl-4-phenylquinolin-2(1H)-one with a molar ratio of 1:1, and N-bromosuccinimide as raw materials, dissolve the above raw materials in N, N-dimethylformamide was stirred at room temperature for 10 hours, and a large amount of solid was precipitated by adding water. The solid was washed and dried to obtain the corresponding bromide with a yield of 80%.

[0093] The second step: under the protection of nitrogen, put the product obtained in the first step and 2-naphthylboronic acid (the molar ratio is 1:1) into a two-neck flask, add a catalytic amount of tetrakis (triphenyl) phosphine palladium) and a mixed solvent (sodium carbonate solution (2mol / L):toluene:ethanol=1:4:4), keep the temperature at 90-100°C, stir for 24 hours, extract with ether, and the product is subjected to column chromatography (eluent is petroleum ether / ethyl acetate ...

Embodiment 3

[0103] Embodiment 3, the preparation of 1-methyl-3-(4-(9-carbazolyl)phenyl)-4-phenylquinolin-2(1H)-one (Q3)

[0104]

[0105] The first step: take 1-methyl-4-phenylquinolin-2(1H)-one with a molar ratio of 1:1, and N-bromosuccinimide as raw materials, and dissolve the above-mentioned raw materials in N, N-dimethylformamide was stirred at room temperature for 10 hours, and a large amount of solid was precipitated by adding water. The solid was washed and dried to obtain the corresponding bromide with a yield of 80%.

[0106] The second step: under the protection of nitrogen, put the product obtained in the first step and 4-(9-carbazolyl)phenylboronic acid (1:1 in molar ratio) into a two-necked bottle, and add a catalytic amount of tetrakis(triphenyl) ) phosphine palladium) and mixed solvent (sodium carbonate solution: toluene: ethanol = 1: 4: 4), keep the temperature at 90-100 ° C, stir for 24 hours, extract with ether, and the product is subjected to column chromatography (e...

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Abstract

The invention discloses quinolone derivatives and preparation method and application thereof. The structural formula of the compounds is shown in the formula I in the specification. As organic light-emitting materials, the compounds can be used for preparing organic light-emitting devices (OLEDs). The OLEDs comprise light-emitting layers, wherein the light-emitting layers contain at least a quinolone derivative to serve as the main material and contain quinolone derivatives or a light-emitting layer formed by the quinolone derivatives, quinolone derivatives or an electron transport layer formed by the quinolone derivatives and quinolone derivatives or a hole blocking layer formed by the quinolone derivatives. The invention further relates to equipment comprising the OLEDs. The quinolone derivatives provided by the invention have appropriate triplet energy levels and obviously improve energy utilization, and when the quinolone derivatives are used for preparing the OLEDs, the prepared devices have satisfactory brightness, current density and efficiency under high current density. The formula I is shown in the specification.

Description

technical field [0001] The invention belongs to the field of organic electroluminescent materials, and in particular relates to quinolone derivatives and a preparation method thereof, as well as the use of the compounds in preparing organic electroluminescent devices. Background technique [0002] In recent years, the research on white light organic electroluminescent materials and devices has received great attention from international academic circles, governments and industries. Countries and regions such as the United States, Europe, Japan, etc. have launched major research programs (NextGeneration Lighting Initiative in the United States, OLLA in the European Union). , Japan 21Century Lighting Program) to strengthen research in this field, the reasons are: First, white organic electroluminescent technology (WOLED), together with inorganic LED technology, may be one of the most important solid-state light source technologies in the new generation. According to statistics...

Claims

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Application Information

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IPC IPC(8): C07D215/227C07D401/10C07D401/14C07D215/38C09K11/06H01L51/50H01L51/54
Inventor 张晓宏黄达郑才俊欧雪梅
Owner TECHNICAL INST OF PHYSICS & CHEMISTRY - CHINESE ACAD OF SCI
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