Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Red light organic electrophosphorescence material metal iridium coordination compound and preparation method thereof, and organic electroluminescent device

A phosphorescent material, metal iridium technology, applied in luminescent materials, electro-solid devices, organic chemistry and other directions, can solve the problem of rarely achieving the color purity of dark red and dark green light, reduce the probability of self-quenching, prepare The effect of easy process control and broad commercial development prospects

Inactive Publication Date: 2014-08-06
OCEANS KING LIGHTING SCI&TECH CO LTD +2
View PDF2 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In order to realize full-color display based on OLED devices, it is generally necessary to obtain red, green and blue materials with excellent performance at the same time. Generally speaking, the development of blue phosphorescent materials always lags behind red and green phosphorescent materials. In terms of this indicator, the luminescence of blue phosphorescent materials has so far rarely achieved the color purity of deep red and deep green light.

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
  • Red light organic electrophosphorescence material metal iridium coordination compound and preparation method thereof, and organic electroluminescent device
  • Red light organic electrophosphorescence material metal iridium coordination compound and preparation method thereof, and organic electroluminescent device
  • Red light organic electrophosphorescence material metal iridium coordination compound and preparation method thereof, and organic electroluminescent device

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0059] A red-light organic electrophosphorescent material metal iridium complex bis[1-methyl-4-phenylphthalazine-N,C 2 '] (acetylacetonate) iridium, as shown in the following structural formula:

[0060]

[0061] The preparation method of the metal iridium complex of the above-mentioned red light organic electrophosphorescent material comprises the following steps:

[0062] (1) Synthesis of cyclometallic main ligand 1-methyl-4-phenylphthalazine, the reaction formula is:

[0063]

[0064] The specific operation is:

[0065] Compound A represented by the following structural formula, i.e. 1-methyl-4-chlorophthalazine, and compound B1, i.e. phenylboronic acid are provided respectively:

[0066]

[0067] Under the protection of nitrogen, 0.72g (4.0mmol) of compound A, 0.59g (4.8mmol) of compound B1 and 0.23g (0.20mmol) of tetrakis (triphenylphosphine) palladium were mixed and dissolved in 15mL of DMF, and the concentration of 1mol was added dropwise to 15mL / L of potas...

Embodiment 2

[0098] A red-light organic electrophosphorescent material metal iridium complex bis[1-methyl-4-(6'-methylphenyl)phthalazine-N,C 2 '] (acetylacetonate) iridium, as shown in the following structural formula:

[0099]

[0100] The preparation method of the metal iridium complex of the above-mentioned red light organic electrophosphorescent material comprises the following steps:

[0101] (1) Synthesis of cyclometallic main ligand 1-methyl-4-(2'-methylphenyl)phthalazine, the reaction formula is:

[0102]

[0103] The specific operation is:

[0104] Compound A represented by the following structural formula, i.e. 1-methyl-4-chlorophthalazine, and compound B2, i.e. 2-methylphenylboronic acid are provided respectively:

[0105]

[0106] Under nitrogen protection, 0.72g (4.0mmol) of compound A, 0.68g (5mmol) of compound B2 and 0.11g (0.16mmol) of dichlorobis(triphenylphosphine)palladium were mixed and dissolved in 15mL of toluene, and the concentration of 10mL was added dro...

Embodiment 3

[0127] A red-light organic electrophosphorescent material metal iridium complex bis[1-methyl-4-(5'-methylphenyl)phthalazine-N,C 2 '] (acetylacetonate) iridium, as shown in the following structural formula:

[0128]

[0129] The preparation method of the metal iridium complex of the above-mentioned red light organic electrophosphorescent material comprises the following steps:

[0130] (1) Synthesis of cyclometallic main ligand 1-methyl-4-(3'-methylphenyl)phthalazine, the reaction formula is:

[0131]

[0132] The specific operation is:

[0133] Compound A represented by the following structural formula, i.e. 1-methyl-4-chlorophthalazine, and compound B3, i.e. 3-methylphenylboronic acid are provided respectively:

[0134]

[0135] Under the protection of nitrogen, mix 0.72g (4.0mmol) compound A, 0.65g (4.8mmol) compound B3 and 0.08g (0.12mmol) dichlorobis(triphenylphosphine)palladium in 20mL DMF, and add dropwise 8mL concentration 1 mol / L potassium carbonate aqueous...

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
Maximum luminescence wavelengthaaaaaaaaaa
Maximum luminescence wavelengthaaaaaaaaaa
Maximum luminescence wavelengthaaaaaaaaaa
Login to View More

Abstract

The present invention provides a red light organic electrophosphorescence material metal iridium coordination compound, which adopts 1-methyl-4-phenyl phthalazine or a derivative as a ring metal main ligand, adopts acetylacetone as an auxiliary ligand, and has a structural formula represented by a formula (1), wherein R is hydrogen or methyl. The preparation method comprises that: a Suzuki coupling reaction is performed to prepare a ring metal main ligand, the ring metal main ligand and IrCl3.3H2O are subjected to polymerization in a 2-ethoxyethanol and water mixed solvent to obtain a chloro-bridge dimer, and the chloro-bridge dimer and acetylacetone are subjected to a ligand exchange reaction to obtain the red light organic electrophosphorescence material metal iridium coordination compound. According to the present invention, 1-methyl-4-phenyl phthalazine or a derivative thereof is adopted as the ring metal main ligand, acetylacetone is adopted as the auxiliary ligand, and the emission wavelength can be adjusted so as to obtain the red light near the standard red color; and the organic electroluminescent device prepared from the material can emit high purity red light, the luminescence efficiency is high, and the preparation method is simple and is suitable for industrial production.

Description

technical field [0001] The invention belongs to the field of organic electroluminescence, and specifically relates to a metal iridium complex of a red light organic electroluminescence material, a preparation method thereof, and an organic electroluminescence device. Background technique [0002] Organic electroluminescence refers to a light-emitting phenomenon in which organic materials directly convert electrical energy into light energy under the action of an electric field. Organic electroluminescent devices (OLEDs) use this type of organic material as a light-emitting material to convert electrical energy into light energy. energy conversion device. Early organic electroluminescent devices had defects such as high driving voltage and low luminous efficiency, which made the research stagnant. To 1987, people such as Tang of American Kodak Company invented 8-hydroxyquinoline aluminum (Alq 3 ) is a luminescent material, and a uniform and dense high-quality thin film is m...

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
IPC IPC(8): C09K11/06C07F15/00H01L51/54
Inventor 周明杰王平张娟娟梁禄生
Owner OCEANS KING LIGHTING SCI&TECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products