IP Library Granted Patent US 10,577,537
Granted Patent B2
US 10,577,537 · App. 16/279,933 · Granted Mar 3, 2020

Light emitting material, manufacture method thereof and organic light emitting diode using the light emitting material

Inventors: Xianjie Li (Shenzhen, CN); Yuanchun Wu (Shenzhen, CN); Shijian Su (Shenzhen, CN); Yunchuan Li (Shenzhen, CN)
Assignee: TCL CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD.
C09K11/06C07D335/16C07D339/08C07D409/14C07D417/14H01L51/0061H01L51/0072H01L51/0074C09K2211/1037H01L51/5012H01L51/5056H01L51/5072H01L51/5092H01L51/5206H01L51/5221H01L51/56
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Quick Facts
Patent No.
US 10,577,537
App. No.
16/279,933
Granted
Mar 3, 2020
Kind
B2
Abstract

A method for manufacturing a light emitting material of the constitutional formula is provided. The structure is unitary, and the formula weight is determined, and the better solubility and film formation are provided, and the thin film status is stable; it possesses a very high decomposition temperature and a lower sublimation temperature, and is easy to sublime to be light emitting material of high purity, and can be applied for small molecule organic light emitting diode. In the method for manufacturing the light emitting material, p-bromothiophenol and 4-Bromo-2-fluorobenzonitrile are employed to be starting materials, and an intermediate of the light emitting material is obtained with a series of simple reactions, and finally, the light emitting material is obtained with Ullmann reaction or Suzuki reaction, and these steps are simple and the production is high.

Claims (18)

1. A method for manufacturing a light emitting material, comprising the following steps:

Step 1, manufacturing an intermediate

Step 2, obtaining a light emitting material with an Ullmann reaction or Suzuki reaction of the intermediate

and an aromatic amine compound, wherein the light emitting material is of the following constitutional formula:

where Ar 1 and Ar 2 are respectively selected from aromatic amine groups shown in formula (1), formula (2), formula (3), formula (4), formula (5), formula (6), and formula (7):

wherein Step 1 comprises:

Step 11, obtaining

with a reaction of p-bromothiophenol and 4-Bromo-2-fluorobenzonitrile,

Step 12, hydrolyzing

in an alkaline condition, and acidizing the same to obtain

Step 13, subjecting

to a dehydration condensation reaction to obtain

and

Step 14, obtaining the intermediate

with a reaction of

and hydrogen peroxide.

2. The method according to claim 1 , wherein Ar 1 and Ar 2 are the same.

3. The method according to claim 2 , wherein the light emitting material is selected from following compound:

Assignments (2)
CHANGE OF NAME Recorded Dec 1, 2019
From: SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD.
To: TCL CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD.
Reel/Frame 051146/0862 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 19, 2019
From: LI, XIANJIE; WU, YUANCHUN; SU, SHIJIAN; LI, YUNCHUAN
To: SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD.
Reel/Frame 048377/0462 →
Priority Claims (1)
CN 2016 1 0579646 · Jul 20, 2016 · national
Continuity (2)
Division 15122410 · Aug 30, 2016
Related Publication 20190177611A1 · Jun 13, 2019