Iridium complex taking dithiolyl ring/aromatic heterocyclic phosphate compound as auxiliary ligand

A technology of iridium complexes and aromatic heterocycles is applied in the fields of electroluminescent devices and organic electroluminescent devices, and can solve problems such as carrier imbalance, lowering device efficiency, etc., achieving simple preparation method, improving electron mobility, high yield effect

Active Publication Date: 2018-09-04
马鞍山南京大学高新技术研究院 +1
View PDF2 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] As we all know, the hole mobility of the hole layer is much greater than the electron mobility of the electron layer, which will lead to the imbalance of carriers and reduce the device efficiency.

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
  • Iridium complex taking dithiolyl ring/aromatic heterocyclic phosphate compound as auxiliary ligand
  • Iridium complex taking dithiolyl ring/aromatic heterocyclic phosphate compound as auxiliary ligand
  • Iridium complex taking dithiolyl ring/aromatic heterocyclic phosphate compound as auxiliary ligand

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] Embodiment 1 Preparation of auxiliary ligand bisthiodiphenyl phosphate sodium aqueous solution

[0034] Reflux bromobenzene and phosphorus trichloride (2:1) in toluene under anaerobic conditions for two hours, separate by column chromatography after cooling to obtain diphenylphosphorus chloride, and then dissolve them with sulfur powder in toluene and anaerobic conditions. Reflux for two hours under conditions, then stir in sodium hydrogensulfide aqueous solution for two hours to obtain dithiodiphenylsodium phosphate aqueous solution The yield reached 100%.

[0035] The above method can be used to prepare other bisthio aromatic ring / heteroaryl ring phosphoric acid compound sodium salt aqueous solution:

Embodiment 2

[0036] The preparation of embodiment 2 iridium complexes of the present invention

[0037] The main ligand 2-phenylpyridine and IrCl 3 Reflux 10 hours in ethoxyethanol solution with the ratio of 2:1, the chlorine bridge complex of iridium obtained by cooling filtration; Refluxed in ethoxyethanol for two hours to obtain the crude product of the iridium complex, and column chromatography yielded 13.80 g of pure SSdpp 1 (yield: 92%). and further placed 5 g of SSdpp 1 in a quartz tube at 10 -5 Heating and sublimation purification under Pa vacuum conditions obtained 4.7 g of luminescent materials (sublimation rate 94%) that met the requirements for device preparation. The response looks like this:

[0038]

[0039] Gained iridium complex SSdpp 1 is analyzed as follows by proton nuclear magnetic resonance spectrum and high-resolution mass spectrometry:

[0040] 1 H NMR (400MHz, CDCl 3 )δ8.56(d,2H),8.16(t,J=7.4Hz,2H),7.82(d,J=4.3Hz,2H),7.52-7.45(m,10H),7.42–7.15(m,14H ), 6....

Embodiment 3

[0046] Preparation of Example 3 Iridium Complex SSdpp 1 Organic Electroluminescent Device

[0047] The preparation of the organic electroluminescent device of the present invention will be described below by taking SSdpp 1 as the luminescent center of the luminescent layer to prepare an organic electroluminescent device as an example. The structure of OLEDs device includes: substrate, anode, hole injection material, hole transport layer, organic light-emitting layer, electron transport layer, electron injection material and cathode. The substrate is glass, the anode is indium tin oxide, and the hole injection layer is 2,3,6,7,10,11-hexacyano-1,4,5,8,9,12-hexaazabenzene Phenanthrene HAT-CN (5nm), the evaporation rate is 0.05nm / s; the hole layer is made of 4,4'-cyclohexylbis[N,N-bis(4-methylphenyl)aniline TAPC material (50nm) , the evaporation rate is 0.05nm / s; the electron transport layer adopts 1,3,5-tris[(3-pyridyl)-3-phenyl]benzene TmPyPb (50nm), the evaporation rate is 0.0...

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
luminanceaaaaaaaaaa
current efficiencyaaaaaaaaaa
Login to view more

Abstract

The invention relates to a novel iridium complex taking heterocyclic nitrogen as a main ligand and taking a dithiolyl ring/aromatic heterocyclic phosphate compound as an auxiliary ligand. The heterocyclic nitrogen and phosphorus-sulfur groups in iridium complex molecules are helpful for increasing the electron mobility of a material and regulating the luminescence color, injection and transmissionof cavity and electrons can be balanced, a composite area of a carrier is widened, the equipment efficiency is increased, and the efficiency roll-off is reduced. The iridium complex has the advantages of simple synthesis, stable chemical properties, easy sublimation purification, and excellent equipment performance, and provides convenience for acquiring a high-efficiency organic electroluminescent device and an application of the high-efficiency organic electroluminescent device in the fields of illumination and display.

Description

technical field [0001] The invention relates to the technical field of organic electroluminescent devices, in particular to a kind of iridium complex luminescent material with dithioaromatic / aromatic heterocyclic phosphoric acid compounds as auxiliary ligands and an electroluminescent device using the material. Background technique [0002] Against the background of increasing global energy demand and worrying ecological environment, governments of various countries have vigorously developed sustainable energy-saving technologies and industries based on high technology. Organic Light-emitting Diode (OLED for short), also known as organic light-emitting diode, is a device in which voltage is applied to convert electrical energy into light energy. Since 1987, Dr. Qingyun Deng of Kodak Company of the United States published OLED with low-voltage start-up, high-efficiency and high-brightness small-molecule organic thin-film double-layer structure, the research on electroluminesc...

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): C07F15/00C09K11/06H01L51/54
CPCC09K11/06C07F15/0033C09K2211/1029C09K2211/1014C09K2211/1044C09K2211/185C09K2211/1088C09K2211/1092C09K2211/1074H10K85/342
Inventor 郑佑轩王毅潘毅左景林苏宁
Owner 马鞍山南京大学高新技术研究院
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
Try Eureka
PatSnap group products