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Organic light emitting compound material and application thereof

A compound and organic technology, applied in silicon organic compounds, luminescent materials, organic chemistry, etc., can solve the problems of lack of efficient and stable main materials, difficulty in achieving full-color RGB, insufficient efficiency, and insufficient lifespan, and achieve good industrialization prospects. Good singlet energy level, color purity improvement effect

Inactive Publication Date: 2017-02-22
JIANGSU SUNERA TECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In addition, for the collocation of OLED devices with different structures, the photoelectric functional materials used have strong selectivity, and the performance of the same material in devices with different structures may be completely different.
[0008] At present, the research of fluorescent materials has made great progress and can meet the needs of industrialization; however, there are still deficiencies in its efficiency and lifespan, and it is difficult to meet the requirements of full-color RGB
The main reason is the lack of efficient and stable host materials; especially for improving device life, the stability of host materials is particularly important

Method used

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  • Organic light emitting compound material and application thereof
  • Organic light emitting compound material and application thereof
  • Organic light emitting compound material and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0053] Example 1 (compound 05)

[0054] The concrete synthetic route of this compound is provided now:

[0055]

[0056] In a 250ml four-neck flask, under nitrogen protection, add 0.01mol compound 1, 0.0105mol o-hydroxyphenylboronic acid, 50ml each of toluene, ethanol, and water, and 0.05g pd (pph 3 ) 4 (Tetraphenyltriphenylphosphine palladium), 0.025mol sodium carbonate, heated to reflux for 12 hours, the reaction was complete; naturally cooled, filtered, the filtrate was rotary evaporated, passed through a silica gel column, and mixed solvent with toluene:ethanol=1:2 (volume ratio) After beating and recrystallization, white intermediate A was obtained.

[0057] In a 250ml four-neck flask, under nitrogen protection, add 0.01mol of intermediate A, 0.025mol of potassium carbonate, 150ml of NMP, and stir for 12 hours at 150°C. After the reaction was complete, it was naturally cooled to room temperature. The reaction solution was added to a separatory funnel, 400ml of wate...

Embodiment 2

[0060] Example 2 (compound 14)

[0061] The concrete synthetic route of this compound is provided now:

[0062]

[0063] In a 250ml four-neck flask, under nitrogen protection, add 0.01mol compound 2, 0.012mol (2-fluorophenyl) phenylamine, 0.03mol sodium tert-butoxide, 1×10 -4 mol Pd 2 (dba) 3 , 1×10 -4 mol tri-tert-butylphosphine, 150ml toluene, heated to reflux for 20 hours, the reaction was complete; naturally cooled, filtered, the filtrate was rotary evaporated, passed through a silica gel column, beaten with a mixed solvent of toluene:ethanol=3:1 (volume ratio), and recrystallized White Intermediate B.

[0064] In a 250ml four-neck flask, under nitrogen protection, add 0.01mol of intermediate B, 0.025mol of potassium carbonate, 150ml of NMP, and stir for 15 hours at 150°C. After the reaction was complete, it was naturally cooled to room temperature. The reaction solution was added to a separatory funnel, 400ml of water was added, extracted three times with ethyl a...

Embodiment 3

[0067] Example 3 (compound 40)

[0068] The concrete synthetic route of this compound is provided now:

[0069]

[0070] 250ml four-necked bottle, under nitrogen protection, add 0.01mol intermediate C, 0.025mol 1-naphthylboronic acid, 0.05g pd (pph 3 ) 4 (tetraphenyltriphenylphosphine palladium), 0.025mol sodium carbonate, each 60ml of toluene, ethanol, water, heated to reflux for 15 hours, the reaction was complete; naturally cooled, filtered, and the filtrate was rotary evaporated, crossed a silica gel column, and used toluene:ethanol=1 : 2 (volume ratio) mixed solvent beating, obtain white solid after recrystallization, purity (HPLC) is 98.5%, yield 62.7%.

[0071] Elemental analysis structure (molecular formula C 53 h 37 N): theoretical value C, 92.54; H, 5.42; N, 2.04;

[0072] Test values: C, 92.61; H, 5.50; N, 1.89.

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Abstract

The invention discloses an organic light emitting compound material and application of the organic light emitting compound material. The structural formula of the compound material is as shown in the general formula (1). The material can form an amorphous thin film easily, is high in heat stability and high in singlet state energy level, and is therefore can be used as a main material of a light emitting layer in an organic light-emitting device.

Description

technical field [0001] The invention relates to the technical field of semiconductors, in particular to the synthesis of a fluorescent compound and its application in an organic light-emitting diode as a host material of a light-emitting layer. 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] Currently, OLED display technology has been applied in smart phones, tablet computers and other fields, and will further expand to large-size applications such as TVs. However, compared with the actual product application requirements, the luminous efficiency and service life of OLED devices need to be further improved. [0004] The OLED light-emitting device is like a sandwich structure, i...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D307/77C07D333/80C07D307/93C07D209/80C07D213/16C07D217/02C07F7/08C07D333/08C07D403/04C07D409/04C07D405/04C07D333/72C07D405/14C07D251/14C07F9/53C07F9/655C07D471/04C07D209/86C07D219/02C07D265/38C07D417/04C07D241/46C07D319/24C07D311/78C07D319/14C07D279/14C07D335/04C07D327/06C07D409/14C07C13/62C09K11/06H01L51/54H01L51/50
CPCC09K11/06C07C13/62C07D209/80C07D209/86C07D213/16C07D217/02C07D219/02C07D241/46C07D251/14C07D265/38C07D279/14C07D307/77C07D307/93C07D311/78C07D319/14C07D319/24C07D327/06C07D333/08C07D333/72C07D333/80C07D335/04C07D403/04C07D405/04C07D405/14C07D409/04C07D409/14C07D417/04C07D471/04C07F7/08C07F9/53C07F9/655C09K2211/1033C09K2211/1037C09K2211/1044C09K2211/1088C09K2211/1092C09K2211/1096C09K2211/1007C09K2211/1011C09K2211/1029H10K85/6576H10K85/657H10K85/6574H10K85/6572H10K50/11
Inventor 叶中华李崇张兆超徐凯张小庆
Owner JIANGSU SUNERA TECH CO LTD
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