Thioxanthone aromatic amine compound and organic light emitting device using the same
US-2016351831-A1 · Dec 1, 2016 · US
US10208013B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10208013-B2 |
| Application number | US-201615122417-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 17, 2016 |
| Priority date | Jul 20, 2016 |
| Publication date | Feb 19, 2019 |
| Grant date | Feb 19, 2019 |
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The present invention provides a light emitting material, a manufacture method thereof and an organic light emitting diode using the light emitting material. 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 manufacture method of the light emitting material according to the present invention, m-bromothiophenol and 4-Bromo-2-fluorobenzonitrile are employed to be starting materials, and the 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 the steps are simple and the production is high.
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What is claimed is: 1. A manufacture method of a light emitting material, comprising steps of: step 1, manufacturing an intermediate step 2, obtaining light emitting material with Ullmann reaction or Suzuki reaction of the intermediate and an aromatic amine compound, in which a constitutional formula of the light emitting material is wherein 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), formula (7); wherein the step 1 comprises: step 11, obtaining with a reaction of m-bromothiophenol and 4-Bromo-2-fluorobenzonitrile; step 12, hydrolyzing in an alkaline condition, and acidizing the same to obtain step 13, generating dehydration condensation reaction to to obtain and step 14, obtaining the intermediate with a reaction of and hydrogen peroxide. 2. The manufacture method of the light emitting material according to claim 1 , wherein Ar 1 and Ar 2 are the same. 3. The manufacture method of the light emitting material according to claim 2 , wherein the light emitting material comprises one or more of following compounds:
containing three or more hetero rings · CPC title
Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 · CPC title
with sulfur · CPC title
containing sulfur as the only heteroatom · CPC title
Electricity · mapped topic
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