Blue light organic electroluminescent material, and preparation method and application thereof

A luminescent and electromechanical technology, applied in luminescent materials, organic chemistry, chemical instruments and methods, etc., can solve the problems of poor blue light color purity, achieve good blue light luminescence performance, simple and easy preparation method, and good film-forming performance Effect

Inactive Publication Date: 2014-12-03
OCEANS KING LIGHTING SCI&TECH CO LTD +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Bis[2-(4',6'-difluorophenyl)pyridine-N,C2'](2-pyridinecarbonyl)iridium (FIrpic, whose structural formula is shown below) disclosed by Holmes R J, Forrest S R et al. (App.Phys.Lett.,2003,82(15):2422-2424) is currently the most reported blue light organic electrophosphoresc...

Method used

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  • Blue light organic electroluminescent material, and preparation method and application thereof
  • Blue light organic electroluminescent material, and preparation method and application thereof
  • Blue light organic electroluminescent material, and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0071] This example provides a bis(2-(2',6'-bis(trifluoromethyl)pyridin-3'-yl)-5-methoxypyrimidine-N,C4')(2,4- Bis(trifluoromethyl)-5-(pyridine-2'-yl)pyrrole) iridium complex, its chemical structure is shown in P1:

[0072]

[0073] The preparation steps of the above P1 are as follows:

[0074] S10. Synthesis of compound C1 (2-(2',6'-bis(trifluoromethyl)pyridin-3'-yl)-5-methoxypyrimidine)

[0075] Compound A1 (2-bromo-5-methoxypyrimidine) and compound B (2,6-bis(trifluoromethyl)pyridine-3-boronic acid) represented by the following structural formulas are provided:

[0076]

[0077] Under nitrogen protection, compound A1 (1.89g, 10mmol), compound B (3.11g, 12mmol) and Pd(PPh 3 ) 4 (0.58mg, 0.5mmol) was dissolved in 35mL of toluene, and then 15mL of an aqueous solution containing potassium carbonate (2.76g, 20mmol) was added, and the reaction was stirred at 90°C for 10 hours; extraction, liquid separation, and then washed to neutrality, then dried with anhydrous magnes...

Embodiment 2

[0102] This example provides a bis(2-(2',6'-bis(trifluoromethyl)pyridin-3'-yl)-4-hexyloxypyrimidine-N,C4')(2,4- Bis(trifluoromethyl)-5-(pyridine-2'-yl)pyrrole) iridium complex, its chemical structure is as shown in P2:

[0103]

[0104] The preparation steps of above-mentioned P2 are as follows:

[0105] S10, Synthesis of Compound C2 (2-(2',6'-bis(trifluoromethyl)pyridin-3'-yl)-5-hexyloxypyrimidine)

[0106] Compound A2 (2-bromo-5-hexyloxypyrimidine) and compound B (2,6-bis(trifluoromethyl)pyridine-3-boronic acid) represented by the following structural formulas are provided:

[0107]

[0108] Under nitrogen protection, compound A2 (1.30g, 5mmol), compound B (1.29g, 5mmol) and Pd(PPh 3 ) 2 Cl 2 (0.14mg, 0.2mmol) was dissolved in 35mL of DMF, and then 15mL of an aqueous solution containing potassium carbonate (2.07g, 15mmol) was added, and stirred at 80°C for 12 hours; after the reaction solution was cooled to room temperature, it was extracted with dichloromethane ,...

Embodiment 3

[0131] This example provides a bis(2-(2',6'-bis(trifluoromethyl)pyridin-3'-yl)-5-eicosyloxypyrimidine-N,C 4' )(2,4-bis(trifluoromethyl)-5-(pyridine-2'-yl)pyrrole) iridium complex, its chemical structure is as shown in P3:

[0132]

[0133] The preparation steps of above-mentioned P3 are as follows:

[0134] S10. Synthesis of compound C3 (2-(2',6'-bis(trifluoromethyl)pyridin-3'-yl)-5-eicosyloxypyrimidine)

[0135] Compound A3 (2-bromo-5-eicosyloxypyrimidine) and compound B (2,6-bis(trifluoromethyl)pyridine-3-boronic acid) represented by the following structural formula are provided:

[0136]

[0137] Under nitrogen protection, compound A3 (0.91g, 2mmol), compound B (0.78g, 3mmol) and Pd(PPh 3 ) 4 (0.07mg, 0.06mmol) was dissolved in 20mL of toluene, then 10mL of an aqueous solution containing sodium carbonate (0.21g, 2mmol) was added, and stirred at 90°C for 15 hours; after the reaction solution was cooled to room temperature, it was extracted with dichloromethane , li...

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Abstract

The invention belongs to the field of photoelectric materials, and specifically relates to a blue light organic electroluminescent material. A structural formula (P) is shown in the description. In the formula, R represents alkoxy of C1-C20. The blue light organic electroluminescent material has a relatively high LUMO energy level and relatively low HOMO energy level, is beneficial to blue shift of luminescent wavelengths of the material. The blue light organic electroluminescent material also has relatively high fluorescence quantum efficiency, relatively good solubility and processability. The invention also provides a preparation method of the blue light organic electroluminescent material, and an application of the blue light organic electroluminescent material in an organic electroluminescent device.

Description

technical field [0001] The invention relates to the field of optoelectronic materials, in particular to a blue-light organic electroluminescent material and its preparation method and application. 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. Due to the limitation of spin statistics theory, the theoretical internal quantum efficiency limit of fluorescent materials is only 25%. How to make full use of the remaining 75% of phosphorescence to achieve higher luminous efficiency has become a hot research direction in this field since then. The complexes of iridium, ruthenium, platinum, etc. can obtain high emission energy from their own triplet state, and the metal iridium (III) compound, due to its good stability, has mild reaction conditions during the synthesis process and has a high electron emission. The lumin...

Claims

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Application Information

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IPC IPC(8): C07F15/00C09K11/06H01L51/54
Inventor 周明杰王平张娟娟陈吉星
Owner OCEANS KING LIGHTING SCI&TECH CO LTD
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