Composite material including selenium, method of fabricating the same, lithium ion and lithium selenium secondary batteries including the same, and lithium ion capacitor including the same
US-2020343540-A1 · Oct 29, 2020 · US
US12207547B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12207547-B2 |
| Application number | US-201816757844-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 9, 2018 |
| Priority date | Nov 10, 2017 |
| Publication date | Jan 21, 2025 |
| Grant date | Jan 21, 2025 |
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The present disclosure relates to an organic electroluminescent compound, an organic electroluminescent material, and an organic electroluminescent device comprising the same. The organic electroluminescent compound of the present disclosure can provide an organic electroluminescent device having improved lifespan properties compared to the organic electroluminescent device comprising a conventional organic electroluminescent compound.
Opening claim text (preview).
The invention claimed is: 1. An organic electroluminescent compound represented by formula 2, 3, 4, 5 or 7: wherein, X 1 to X 3 each independently represent CR 12 or N; at least one of X 1 to X 3 represents N; Ar 1 to Ar 3 each independently represent a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl; R 1 to R 3 , and R 12 each independently represent hydrogen, deuterium, halogen, cyano, carboxyl, nitro, hydroxyl, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C3-C30)cycloalkenyl, a substituted or unsubstituted (3- to 7-membered)heterocycloalkyl, a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl; or R 1 and R 3 may be linked to an adjacent substituent to form a substituted or unsubstituted (C3-C30) mono- or polycyclic, alicyclic or aromatic ring or a combination thereof; a and b each independently represent an integer from 0 to 4; c represents an integer from 0 to 2; when a or b is an integer of 2 or more or c is 2, each of R 1 , each of R 2 , or each of R 3 may be the same or different; L 1 is represented by the following formula R-1: wherein, R 4 represents hydrogen, deuterium, halogen, cyano, carboxyl, nitro, hydroxyl, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C3-C30)cycloalkenyl, a substituted or unsubstituted (3- to 7-membered)heterocycloalkyl, a substituted or unsubstituted (C6-C30)aryl or a substituted or unsubstituted (3- to 30-membered)heteroaryl; d represents an integer from 0 to 6, when d is an integer of 2 or more, each of R 4 may be the same or different; * represents a linkage position with an adjacent ring in formula 1. 2. The organic electroluminescent compound according to claim 1 , wherein the substituents of the substituted (C1-C30)alkyl, the substituted (C3-C30)cycloalkyl, the substituted (C3-C30)cycloalkenyl, the substituted (3- to 7-b membered)heterocycloalkyl, the substituted (C6-C30)aryl, the substituted (3- to 30-membered)heteroaryl, and the substituted (C3-C30) mono- or polycyclic, alicyclic, or aromatic ring, or a combination thereof in Ar 1 to Ar 3 , R 1 to R 4 , and R 12 , each independently, are at least one selected from the group consisting of deuterium, halogen, cyano, carboxyl, nitro, hydroxyl, (C1-C30)alkyl, halo(C1-C30)alkyl, (C2-C30)alkenyl, (C2-C30)alkynyl, (C1-C30)alkoxy, (C1-C30)alkylthio, (C3-C30)cycloalkyl, (C3-C30)cycloalkenyl, (3- to 7-membered)heterocycloalkyl, (C6-C30)aryloxy, (C6-C30)arylthio, unsubstituted (5- to 30-membered)heteroaryl, (5- to 30-membered)heteroaryl substituted with (C6-C30)aryl, unsubstituted (C6-C30)aryl, (C6-C30)aryl substituted with (5- to 30-membered)heteroaryl, tri(C1-C30)alkylsilyl, tri(C6-C30)arylsilyl, di(C1-C30)alkyl(C6-C30)arylsilyl, (C1-C30)alkyldi(C6-C30)arylsilyl, amino, mono- or di-(C1-C30)alkylamino, unsubstituted mono- or di-(C6-C30)arylamino, mono- or di-(C6-C30)arylamino substituted with (C1-C30)alkyl, (C1-C30)alkyl(C6-C30)arylamino, (C1-C30)alkylcarbonyl, (C1-C30)alkoxycarbonyl, (C6-C30)arylcarbonyl, di(C6-C30)arylboronyl, di(C1-C30)alkylboronyl, (C1-C30)alkyl(C6-C30)arylboronyl, (C6-C30)aryl(C1-C30)alkyl, and (C1-C30)alkyl(C6-C30)aryl. 3. The organic electroluminescent compound according to claim 1 , wherein at least two of X 1 to X 3 represent N; Ar 1 to Ar 3 each independently represent a substituted or unsubstituted (C6-C25)aryl; R 1 to R 4 , and R 12 each independently represent hydrogen or deuterium. 4. The organic electroluminescent compound according to claim 1 , wherein the compound represented by formula 2 to 5 or 7 is selected from the following compounds: 5. An organic electroluminescent material comprising the organic electroluminescent compound according to claim 1 . 6. An organic electroluminescent device comprising the organic electroluminescent compound according to claim 1 .
Triplet emission · CPC title
characterised by the electroluminescent [EL] layers · CPC title
comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole · CPC title
Heterocyclic compounds · CPC title
Condensed systems · CPC title
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