Heterocyclic compound, organic light-emitting device including the same, and electronic apparatus including the organic light-emitting device
US-2024373662-A1 · Nov 7, 2024 · US
US10069077B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10069077-B2 |
| Application number | US-201514644158-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 10, 2015 |
| Priority date | Sep 12, 2014 |
| Publication date | Sep 4, 2018 |
| Grant date | Sep 4, 2018 |
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A compound for an organic light-emitting device, the compound represented by Chemical Formula 1 and satisfying Mathematical Formula 1: E S1 <2E T1 <E T2 , Mathematical Formula 1 wherein, in Mathematical Formula 1, E S1 is a first singlet energy of the compound; E T1 is a first triplet energy of the compound; and E T2 is a second triplet energy of the compound.
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What is claimed is: 1. A compound for an organic light-emitting device, the compound satisfying Mathematical Formula 1 and being represented by one selected from the group consisting of Chemical Formulae 1A-1 to 1A-6: wherein, in Chemical Formulae 1A-1 and 1A-2, R 12 , R 13 , R 15 , R 17 , R 18 and R 20 are each independently selected from the group consisting of —F, a methyl group, an ethyl group, an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, —Si(CH 3 ) 3 , and compounds represented by Chemical Formulae 3-1 and 3-2, and in Chemical Formulae 1A-3 to 1A-6, R 12 , R 13 , R 15 , R 17 , R 18 and R 20 are each independently selected from the group consisting of a hydrogen atom, —F, a methyl group, an ethyl group, an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, —Si(CH 3 ) 3 , and compounds represented by Chemical Formulae 3-1 and 3-2: wherein, in Chemical Formulae 3-1 and 3-2, * is a binding site to an adjacent atom; E S1 <2E T1 <E T2 , Mathematical Formula 1 wherein, in Mathematical Formula 1, E S1 is a first singlet energy of the compound, E S1 being in a range of about 3.1 eV to about 3.3 eV; E T1 is a first triplet energy of the compound; and E T2 is a second triplet energy of the compound. 2. The compound of claim 1 , wherein Chemical Formulae 1A-1 to 1A-6 satisfy Chemical Formula 1, wherein a first triplet energy (E AT1 ) of A and a first triplet energy (E BT1 ) of B satisfy Mathematical Formula 2: E AT1 <E BT1 . Mathematical Formula 2 3. The compound of claim 2 , wherein a second triplet energy (E AT2 ) of A and a first triplet energy (E BT1 ) of B satisfy Mathematical Formula 3: E AT2 <E BT1 . Mathematical Formula 3 4. The compound of claim 1 , wherein the compound is selected from Compounds 1 to 10: 5. An organic light-emitting device comprising: a first electrode; a second electrode; and an organic layer between the first electrode and the second electrode, the organic layer comprising an emission layer, wherein the emission layer comprises the compound of claim 1 . 6. The organic light-emitting device of claim 5 , wherein the emission layer comprises a dopant and the compound as a host. 7. The organic light-emitting device of claim 5 , wherein the emission layer comprises a host and the compound as a dopant. 8. The compound of claim 1 , wherein E T1 is in a range of about 1.3 eV to about 1.7 eV, and E T2 is in a range of about 2.8 eV to about 3.5 eV.
Condensed systems · CPC title
Nitrogen atoms · CPC title
bridged by heteroatoms, e.g. N, P, Si or B · CPC title
containing two nitrogen atoms as heteroatoms · CPC title
containing one nitrogen atom as the heteroatom · CPC title
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