Radiomitigating pharmaceutical formulations
US-9783515-B2 · Oct 10, 2017 · US
US11718583B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11718583-B2 |
| Application number | US-202117789557-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 8, 2021 |
| Priority date | Apr 30, 2020 |
| Publication date | Aug 8, 2023 |
| Grant date | Aug 8, 2023 |
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The present disclosure belongs to the field of organic electroluminescent materials, and specifically relates to a nitrogen-containing compound, an electronic component using the nitrogen-containing compound and an electronic device using the nitrogen-containing compound. The nitrogen-containing compound has a structure as shown in Formula 1. When the nitrogen-containing compound of the present disclosure is used in an organic electroluminescent device, properties of the device can be effectively improved.
Opening claim text (preview).
What is claimed is: 1. A nitrogen-containing compound, having a structure represented by Formula 1: wherein X is selected from O, S, N(R 4 ), or C(R 5 R 6 ), R 4 is selected from an aryl with 6 to 12 carbon atoms, or a heteroaryl with 3 to 12 carbon atoms; R 5 to R 6 are each independently selected from an alkyl with 1 to 4 carbon atoms, or an aryl with 6 to 12 carbon atoms; Ar is selected from a substituted or unsubstituted aryl with 6 to 26 carbon atoms, or a substituted or unsubstituted heteroaryl with 3 to 24 carbon atoms; L is selected from single bond, or a substituted or unsubstituted arylene with 6 to 20 carbon atoms; A has a structure represented by the following Formula 1-1 or Formula 1-2: the substituents in L and Ar are the same or different, and are each independently selected from deuterium, fluorine, cyano, an alkyl with 1 to 4 carbon atoms, an alkoxy with 1 to 4 carbon atoms, an alkylthio with 1 to 4 carbon atoms, a haloalkyl with 1 to 4 carbon atoms, a cycloalkyl with 5 to 10 carbon atoms, an aryl with 6 to 15 carbon atoms, a heteroaryl with 5 to 12 carbon atoms, a trialkylsilyl with 3 to 7 carbon atoms, or triphenylsilyl; in L and Ar, optionally, any two adjacent substituents form a ring; R 1 to R 3 are the same or different, and are each independently selected from deuterium, fluorine, cyano, an alkyl with 1 to 4 carbon atoms, an alkoxy with 1 to 4 carbon atoms, an alkylthio with 1 to 4 carbon atoms, a fluoroalkyl with 1 to 4 carbon atoms, a cycloalkyl with 5 to 10 carbon atoms, a trialkylsilyl with 3 to 7 carbon atoms, or an aryl with 6 to 12 carbon atoms; and n 1 , n 2 and n 3 respectively represent the number of R 1 , R 2 and R 3 ; R 1 to R 3 are represented by R j , and n 1 to n 3 are represented by n j , wherein j is a variable representing an integer of 1 to 3; and when j is 1, n j is selected from 0, 1, 2, 3, or 4; when j is 2, n j is selected from 0, 1, 2, or 3; when j is 3, n j is 0, 1, 2, 3, 4, 5, 6, or 7; optionally, any two adjacent R j form a ring. 2. The nitrogen-containing compound of claim 1 , wherein R 1 and R 2 are each independently selected from deuterium, fluorine, cyano, methyl, ethyl, n-propyl, isopropyl, tert-butyl, methoxy, trifluoromethyl, cyclopentyl, cyclohexyl, trimethylsilyl, phenyl, per or naphthyl. 3. The nitrogen-containing compound of claim 1 , wherein Ar is a substituted or unsubstituted group V 1 , the unsubstituted group V 1 is selected from the following groups: the substituted group V 1 has one or two or more substituents, the substituents in the substituted group V 1 are independently selected from deuterium, fluorine, cyano, an alkyl with 1 to 4 carbon atoms, an alkoxy with 1 to 4 carbon atoms, an alkylthio with 1 to 4 carbon atoms, a fluoroalkyl with 1 to 4 carbon atoms, a cycloalkyl with 5 to 10 carbon atoms, a trialkylsilyl with 3 to 7 carbon atoms, or pyridyl. 4. The nitrogen-containing compound of claim 1 , wherein L is selected from single bond, or a substituted or unsubstituted group V 2 , the unsubstituted group V 2 is selected from the following groups: the substituted group V 2 has one or two or more substituents, and the substituents in the substituted group V 2 are independently selected from deuterium, fluorine, cyano, an alkyl with 1 to 4 carbon atoms, an alkoxy with 1 to 4 carbon atoms, an alkylthio with 1 to 4 carbon atoms, a fluoroalkyl with 1 to 4 carbon atoms, a cycloalkyl with 5 to 10 carbon atoms, a trialkylsilyl with 3 to 7 carbon atoms, an aryl with 6 to 12 carbon atoms, or triphenylsilyl. 5. The nitrogen-containing compound of claim 1 , wherein X is selected from O, S, N(Ph), or C(CH 3 ) 2 , and n 3 is selected from 0 or 1; R 3 is selected from methyl, tert-butyl, fluorine, cyano, or trimethylsilyl; and Ar is selected from dibenzofuryl, dibenzothiophenyl, 9,9-dimethylfluorenyl, or N-phenylcarbazolyl. 6. The nitrogen-containing compound of claim 1 , wherein the nitrogen-containing compound is selected from the following compounds:
Sulfur atoms · CPC title
the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being further bound to other hetero atoms · CPC title
Carbazoles; Hydrogenated carbazoles · CPC title
having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom · CPC title
Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals · CPC title
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