Method for preparing anti-hardening granulous ceramic iron-carbon micro-electrolysis filler by using industrial waste
US-9428407-B2 · Aug 30, 2016 · US
US9705086B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9705086-B2 |
| Application number | US-201314108664-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 17, 2013 |
| Priority date | Dec 27, 2012 |
| Publication date | Jul 11, 2017 |
| Grant date | Jul 11, 2017 |
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A blue fluorescent compound is disclosed. The blue fluorescent compound represented by the following Chemical Formula 1, where R1 and R2 are each independently selected from the group consisting of C0-C18 saturated hydrocarbon carbons, branched saturated hydrocarbons, and saturated ring hydrocarbons, and Ar1 and Ar2 are each independently selected from the group consisting of C1-C20 aromatic compounds, heteroaromatic compounds, C1-C18 saturated hydrocarbons, C1-C18 branched saturated hydrocarbons, and C1-C18 saturated ring hydrocarbons.
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What is claimed is: 1. A blue fluorescent compound represented by the following Chemical Formula 1: where R 1 and R 2 are each selected from the group consisting of H, C 1 -C 18 saturated hydrocarbon carbons, branched saturated hydrocarbons, and saturated ring hydrocarbons, and Ar 1 is selected from the group consisting of C 1 -C 20 aromatic compounds, heteroaromatic compounds, C 1 -C 18 saturated hydrocarbons, C 1 -C 18 branched saturated hydrocarbons, and C 1 -C 18 saturated ring hydrocarbons; and Ar 2 is a heteroaromatic compound selected from the group consisting of: wherein R is H, methyl, ethyl, isopropyl, tertiary-butyl, n-butyl, 1,3,5-trimethylhexyl, or aryl. 2. The blue fluorescent compound of claim 1 , wherein R 1 and R 2 are each selected from: H, methyl, ethyl, isospropyl, tertiary-butyl, n-butyl, and 1,3,5-trimethylhexyl. 3. The blue fluorescent compound of claim 1 , wherein Ar 1 is selected from the group consisting of: wherein R is wherein R is H, methyl, ethyl, isopropyl, tertiary-butyl, n-butyl, 1,3,5-trimethylhexyl, or aryl. 4. The blue fluorescent compound of claim 1 , wherein the blue fluorescent compound is any one selected from the compounds represented below: 5. An organic light emitting diode device comprising an organic film formed between an anode and a cathode, the organic film comprising the blue fluorescent compound of claim 1 . 6. The organic light emitting diode device of claim 5 , wherein the organic film is an emission layer. 7. The organic light emitting diode device of claim 5 , wherein the compound is used as the host of the emission layer. 8. The organic light emitting diode device of claim 5 , further comprising one or more selected from the group consisting of a hole injection layer, a hole transport layer, an electron transport layer, and an electron injection layer between the anode and the cathode. 9. The blue fluorescent compound of claim 1 , wherein Ar 2 is selected from: 10. The blue fluorescent compound of claim 9 , wherein the R substituent on Ar 2 is H or aryl.
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