Cyclic azine compound, material for organic light emitting diode, electron transport material for organic light emitting diode, and organic light emitting diode
US-2022274952-A1 · Sep 1, 2022 · US
US11889754B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11889754-B2 |
| Application number | US-202016985079-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 4, 2020 |
| Priority date | Aug 14, 2019 |
| Publication date | Jan 30, 2024 |
| Grant date | Jan 30, 2024 |
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The present disclosure provides an organic compound of the following formula and an organic light emitting diode and an OLED device including the same.
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What is claimed is: 1. An organic compound represented by the following Formula 1: wherein: each of X 1 , X 2 and X 3 is independently selected from carbon (C) and nitrogen (N), provided that at least one of X 1 to X 3 is N, and each of Z 1 , Z 2 and Z 3 is independently selected from a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C5 to C30 heteroaryl group, a substituted or unsubstituted C1 to C12 alkyl group, a substituted or unsubstituted C1 to C12 alkoxy group, a substituted or unsubstituted C1 to C12 ether group, halogen, cyano (CN), trimethylsilyl, Formula 2, Formula 3 and Formula 4, provided that at least one of Z 1 to Z 3 is represented by one of the following Formulas 2 to 4, wherein in Formula 2, each of X 11 and X 12 is independently selected from C and N, provided that at least one of X 11 and X 12 is N, each of X 13 to X 16 is independently selected from C and N, R 1 is selected from a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C5 to C30 heteroaryl group, a substituted or unsubstituted C1 to C12 alkyl group, a substituted or unsubstituted C1 to C12 alkoxy group, cyano, halogen and trifluoromethyl, and m1 is an integer of 0 to 4, wherein in Formula 3, each of X 21 and X 22 is independently selected from C and N, provided that at least one of X 21 and X 22 is N, R 2 is selected from cyano and phenyl, R 3 is selected from a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C5 to C30 heteroaryl group, a substituted or unsubstituted C1 to C12 alkyl group, a substituted or unsubstituted C1 to C12 alkoxy group, cyano, halogen and trifluoromethyl, and m2 is an integer of 0 to 3, wherein in Formula 4, each of X 31 and X 32 is independently selected from N and oxygen (O), provided that when one of X 31 and X 32 is N, then the other one of X 31 and X 32 is O, each of X 33 to X 36 is independently selected from C and N, R 4 is selected from a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C5 to C30 heteroaryl group, a substituted or unsubstituted C1 to C12 alkyl group, a substituted or unsubstituted C1 to C12 alkoxy group, cyano, halogen and trifluoromethyl, and m3 is an integer of 0 to 4. 2. The organic compound of claim 1 , wherein at least one of X 13 to X 16 is C, and R 1 is selected from methyl, trifluoromethyl, trifluoromethoxy, cyano and fluorine (F). 3. The organic compound of to claim 1 , wherein R 2 is phenyl substituted by at least one of F and CN, and R 3 is CN. 4. The organic compound of claim 1 , wherein at least one of X 33 to X 36 is C, and R 4 is selected from F, CN and trifluoromethyl. 5. The organic compound of claim 1 , wherein the organic compound has one of the following structures:
Electron injection layers · CPC title
Carrier injection layers · CPC title
comprising only nitrogen as heteroatom (H10K85/652 takes precedence) · CPC title
containing three or more hetero rings · CPC title
linked by a carbon chain containing aromatic rings · CPC title
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