Compound and organic electroluminescent device

A compound and organic layer technology, applied in the field of organic heterocyclic compounds, can solve problems such as unfavorable energy saving, increased device operating voltage, and reduced device luminous efficiency, and achieve excellent device performance.

Active Publication Date: 2020-02-21
TSINGHUA UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Generally speaking, electron-transporting materials are compounds with electron-deficient nitrogen-containing heterocyclic groups. Most of them have high electron affinity, so they have a strong ability to accept electrons. , common electron transport materials such as AlQ 3 The electron mobility of (octahydroxyquinoline aluminum) is much lower than the hole mobility of the hole transport material, so in the OLED device, on the one hand, i

Method used

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  • Compound and organic electroluminescent device
  • Compound and organic electroluminescent device
  • Compound and organic electroluminescent device

Examples

Experimental program
Comparison scheme
Effect test

Embodiment

[0094] The specific preparation method of the above-mentioned novel compound of the present invention will be described in detail below by taking several examples as examples, but the preparation method of the present invention is not limited to these examples.

[0095] Various chemicals used in the present invention such as petroleum ether, ethyl acetate, sodium sulfate, toluene, tetrahydrofuran, dichloromethane, acetic acid, potassium phosphate, sodium tert-butoxide and other basic chemical raw materials are all purchased from common chemical products on the market Providers, including but not limited to Shanghai Titan Technology Co., Ltd. and Xilong Chemical Co., Ltd. The mass spectrometer used to determine the following compounds was a ZAB-HS mass spectrometer (manufactured by Micromass, UK). In the present invention, the nuclear magnetic resonance is measured by a BRUKER 500MHZ nuclear magnetic resonance instrument (manufactured by BRUKER, Germany).

[0096] Synthetic e...

Embodiment 1

[0155] Using the compound C1 of the present invention as an electron transport material, an organic electroluminescent device was prepared according to the above-mentioned preparation process of the organic electroluminescent device, and the device performance was tested according to the above-mentioned organic electroluminescent device testing method.

Embodiment 2

[0157] An organic electroluminescence device was prepared by the same method as in Example 1, except that the compound C1 was replaced by C3.

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Abstract

The invention provides a novel organic electroluminescent material for an organic electroluminescent device, and the organic electroluminescent device using the novel organic electroluminescent material. The novel organic electroluminescent material provided by the present invention is represented by a formula (I) as described in the description.

Description

technical field [0001] The invention relates to a new organic heterocyclic compound which can be used as an organic electroluminescent material, in particular to a compound containing anthracene structure and its application in organic electroluminescent devices. Background technique [0002] At present, with the continuous advancement of OLED technology in the two major fields of display and lighting, people pay more attention to the research of its core materials. As core materials, common functional organic materials include: hole injection materials, hole transport materials, hole blocking materials, electron injection materials, electron transport materials, electron blocking materials, and luminescent host materials and luminescent objects (dye). [0003] Various types of electron transport materials with strong transport capacity and high stability have been reported in previous articles and patents. Generally speaking, electron-transporting materials are compounds w...

Claims

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Application Information

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IPC IPC(8): C07D401/10C07D403/10C07D401/14C07D409/14C07D405/14H01L51/50H01L51/54
CPCC07D401/10C07D403/10C07D401/14C07D409/14C07D405/14C09K11/06H10K85/626H10K85/615H10K85/6576H10K85/6574H10K85/6572H10K50/18H10K50/16
Inventor 段炼高文正邵爽
Owner TSINGHUA UNIV
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