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
US2024284697A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2024284697-A1 |
| Application number | US-202318482327-A |
| Country | US |
| Kind code | A1 |
| Filing date | Oct 6, 2023 |
| Priority date | Feb 2, 2023 |
| Publication date | Aug 22, 2024 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A light-emitting device including an anode, a cathode, a first emission layer arranged on the anode and including a first phosphorescent emitter, and a second emission layer arranged on the first emission layer and including a first fluorescent emitter and a second phosphorescent emitter.
Opening claim text (preview).
What is claimed is: 1 . A light-emitting device comprising: an anode; a cathode facing the anode; a first emission layer arranged on the anode and comprising a first phosphorescent emitter; and a second emission layer arranged on the first emission layer and comprising a first fluorescent emitter and a second phosphorescent emitter, wherein a decay time T decay (1) of the first emission layer is shorter than a decay time T decay (2) of the second emission layer. 2 . The light-emitting device of claim 1 , wherein the first emission layer and the second emission layer each independently comprise at least one of a first host or a second host. 3 . The light-emitting device of claim 2 , wherein the first host is a hole-transporting host, and the second host is an electron-transporting host. 4 . The light-emitting device of claim 2 , wherein the first host comprises at least one carbazole moiety, and the second host comprises at least one azine moiety. 5 . The light-emitting device of claim 2 , wherein the first host comprises a compound represented by Formula 1: wherein, in Formulae 1 and 1A, CY 11 to CY 14 are each independently an unsubstituted or substituted C 5 -C 30 carbocyclic group or an unsubstituted or substituted C 1 -C 30 heterocyclic group, E 1 is a group represented by Formula 1A, k 1 is an integer from 0 to 5, n11 is an integer from 0 to 3, n12 is an integer from 0 to 3, R 11 to R 17 are each independently deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C 1 -C 60 alkyl group, a substituted or unsubstituted C 2 -C 60 alkenyl group, a substituted or unsubstituted C 2 -C 60 alkynyl group, a substituted or unsubstituted C 1 -C 60 alkoxy group, a substituted or unsubstituted C 3 -C 10 cycloalkyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkyl group, a substituted or unsubstituted C 3 -C 10 cycloalkenyl group, a substituted or unsubstituted C 2 -C 10 heterocycloalkenyl group, a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 6 -C 60 aryloxy group, a substituted or unsubstituted C 6 -C 60 arylthio group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, a substituted or unsubstituted C 1 -C 60 heteroaryloxy group, a substituted or unsubstituted C 1 -C 60 heteroarylthio group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —Si(Q 1 )(Q 2 )(Q 3 ), —Ge(Q 1 )(Q 2 )(Q 3 ), —N(Q 4 )(Q 5 ), —B(Q 6 )(Q 7 ), or —P(═O)(Q 8 )(Q 9 ), b15 and b16 are each independently an integer from 0 to 4, b17 is an integer from 0 to 5, b11 to b14 are each independently an integer from 0 to 10, * indicates a binding site to a neighboring atom, wherein Q 1 to Q 9 , are each independently hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C 1 -C 30 alkyl group, a substituted or unsubstituted C 2 -C 30 alkenyl group, a substituted or unsubstituted C 2 -C 30 alkynyl group, a substituted or unsubstituted C 1 -C 30 alkoxy group, a substituted or unsubstituted C 3 -C 10 cycloalkyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkyl group, a substituted or unsubstituted C 3 -C 10 cycloalkenyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkenyl group, a substituted or unsubstituted C 6 -C 30 aryl group, a substituted or unsubstituted C 6 -C 30 aryloxy group, a substituted or unsubstituted C 6 -C 30 arylthio group, a substituted or unsubstituted C 1 -C 30 heteroaryl group, a substituted or unsubstituted C 1 -C 30 heteroaryloxy group, a substituted or unsubstituted C 1 -C 30 heteroarylthio group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, or a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group. 6 . The light-emitting device of claim 2 , wherein the second host comprises a compound represented by Formula 2: wherein, in Formula 2, CY 23 and CY 24 are each independently a C 5 -C 30 carbocyclic group or a C 1 -C 30 heterocyclic group, X 21 is N or C(R 21a ), X 22 is N or C(R 22a ), X 23 is N or C(R 23a ), and at least one of X 21 to X 23 is N, L 21 and L 22 are each independently a single bond, a substituted or unsubstituted C 3 -C 60 carbocyclic group, or a substituted or unsubstituted C 1 -C 60 heterocyclic group, n21 and n22 are each independently an integer from 1 to 5, R 21 to R 24 , R 21a , R 22a , and R 23a are each independently deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C 1 -C 60 alkyl group, a substituted or unsubstituted C 2 -C 60 alkenyl group, a substituted or unsubstituted C 2 -C 60 alkynyl group, a substituted or unsubstituted C 1 -C 60 alkoxy group, a substituted or unsubstituted C 3 -C 10 cycloalkyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkyl group, a substituted or unsubstituted C 3 -C 10 cycloalkenyl group, a substituted or unsubstituted C 2 -C 10 heterocycloalkenyl group, a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 6 -C 60 aryloxy group, a substituted or unsubstituted C 6 -C 60 arylthio group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, a substituted or unsubstituted C 1 -C 60 heteroaryloxy group, a substituted or unsubstituted C 1 -C 60 heteroarylthio group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —Si(Q 1 )(Q 2 )(Q 3 ), —Ge(Q 1 )(Q 2 )(Q 3 ), —N(Q 4 )(Q 5 ), —B(Q 6 )(Q 7 ), or —P(═O)(Q 8 )(Q 9 ), b21 to b24 are each independently an integer from 1 to 10, wherein Q 1 to Q 9 , are each independently hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C 1 -C 30 alkyl group, a substituted or unsubstituted C 2 -C 30 alkenyl group, a substituted or unsubstituted C 2 -C 30 alkynyl group, a substituted or unsubstituted C 1 -C 30 alkoxy group, a substituted or unsubstituted C 3 -C 10 cycloalkyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkyl group, a substituted or unsubstituted C 3 -C 10 cycloalkenyl group, a substituted or unsubstituted C 1 -C 10 heterocycloalkenyl group, a substituted or unsubstituted C 6 -C 30 aryl group, a substituted or unsubstituted C 6 -C 30 aryloxy group, a substituted or unsubstituted C 6 -C 30 arylthi
Metal complexes comprising a group IB metal element, e.g. comprising copper, gold or silver · CPC title
Transition metal complexes, e.g. Ru(II)polypyridine complexes (H10K85/331 takes precedence) · CPC title
comprising platinum · CPC title
Coordination compounds · CPC title
comprising dopants · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.