Heterocyclic compound, organic light-emitting element comprising same, and composition for organic material layer
US-2024298525-A1 · Sep 5, 2024 · US
US10961447B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10961447-B2 |
| Application number | US-202016737913-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 9, 2020 |
| Priority date | Jul 20, 2016 |
| Publication date | Mar 30, 2021 |
| Grant date | Mar 30, 2021 |
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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.
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What is claimed is: 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 Ar 1 and Ar 2 are the same; wherein the light emitting material is selected from the following compound: 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.
containing one nitrogen atom as the heteroatom · CPC title
containing three or more hetero rings · CPC title
containing three or more hetero rings · CPC title
containing organic luminescent materials · CPC title
Oxygen atoms, e.g. thioxanthones · CPC title
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