IP Library › Granted Patent US 12,495,718
Granted Patent B2
US 12,495,718 · App. 17/293,896 · Granted Dec 9, 2025

Compound and organic light emitting device comprising same

Inventors: Minjun Kim (Daejeon, KR); Dong Hoon Lee (Daejeon, KR); Hyoung Seok Kim (Daejeon, KR); Sangwoo Lee (Daejeon, KR); Sang Duk Suh (Daejeon, KR); Donghee Kim (Daejeon, KR); Sunmin Kim (Daejeon, KR); Da Jung Lee (Daejeon, KR)
Assignee: LG CHEM, LTD.
H10K85/6572C07D403/14C07D405/14C07D409/14C09K11/06H10K85/615H10K85/6574H10K85/6576C09K2211/1018H10K50/11H10K2101/10
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Quick Facts
Patent No.
US 12,495,718
App. No.
17/293,896
Granted
Dec 9, 2025
Kind
B2
Abstract

A compound of Chemical Formula 1: where at least one of R7 to R10 is Chemical Formula A, and the remaining R7 to R10 are hydrogen: wherein in Chemical Formula A, means a bond with R7 to R10; R15 is hydrogen, a nitrile group, a halogen group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heteroaryl group, or adjacent groups bond to each other to form a substituted or unsubstituted ring; and the other substituents are as defined in the specification, and an organic light emitting device including the same.

Claims (18)

1 . A compound of Chemical Formula 1:

wherein, in Chemical Formula 1:

L is a direct bond;

a is CR and b is N;

R is an aryl group selected from among a phenyl group, a naphthyl group, a biphenyl group, a terphenyl group, an anthracene group, a phenanthrene group, a fluorene group, a triphenylene group or a pyrene group, and the phenyl group, the naphthyl group, the biphenyl group, the terphenyl group, the anthracene group, the phenanthrene group, the fluorene group, the triphenylene group or the pyrene group is unsubstituted or substituted with any one or more selected from among a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a tert-butyl group, a phenyl group, a biphenyl group, a naphthyl group, an anthracene group, a phenanthrene group, a terphenyl group, and a triphenyl group, or a heteroaryl group selected from among a pyridine group, a pyrimidine group, a triazine group, a dibenzofuran group, a dibenzothiophene group or a carbazole group, and the pyridine group, the pyrimidine group, the triazine group, the dibenzofuran group, the dibenzothiophene group or the carbazole group is unsubstituted or substituted with a phenyl group, a biphenyl group, a terphenyl group, an anthracene group, a phenanthrene group, or a naphthyl group;

R1 to R6 and R11 to R14 are hydrogen; and

at least one of R7 to R10 is Chemical Formula A, and the remaining R7 to R10 are hydrogen:

wherein in Chemical Formula A:

means a bond with R7 to R10;

R15 is hydrogen, or adjacent groups bond to each other to form a benzene ring, provided that Chemical Formula A is not a dibenzocarbazole group; and

r15 is an integer of 0 to 8.

2 . The compound of claim 1 , wherein the compound of Chemical Formula 1 is any one compound selected from among the following compounds:

3 . An organic light emitting device comprising:

a first electrode;

a second electrode; and

one or more organic material layers provided between the first electrode and the second electrode,

wherein at least one of the one or more organic material layers is a red light emitting layer, and the red light emitting layer includes the compound of Chemical Formula 1 of claim 1 .

4 . The compound of claim 1 , wherein R is a phenyl group; a phenyl group substituted with a naphthyl group; a naphthyl group; a naphthyl group substituted a phenyl group; a biphenyl group; a terphenyl group; a phenanthrene group; a fluorene group substituted with a methyl group; a dibenzofuran group; a dibenzothiophene group; or a carbazole group that is unsubstituted or substituted with a phenyl group.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2021
From: KIM, MINJUN; LEE, DONG HOON; KIM, HYOUNG SEOK; LEE, SANGWOO; SUH, SANG DUK; KIM, DONGHEE; KIM, SUNMIN; LEE, DA JUNG
To: LG CHEM, LTD.
Reel/Frame 056236/0640 →
Priority Claims (1)
KR 10-2019-0024135 · Feb 28, 2019 · national
Continuity (1)
Related Publication 20220029107A1 · Jan 27, 2022
References Cited (33)
US 9190618B2 · Bae et al. · 2015 [cited by applicant]
US 9698358B2 · Hong · 2017 [cited by examiner]
US 9768393B2 · Shin et al. · 2017 [cited by applicant]
US 9947878B2 · Chun · 2018 [cited by examiner]
US 10186669B2 · Kang et al. · 2019 [cited by applicant]
US 20140100367A1 · Yoon et al. · 2014 [cited by applicant]
US 20150060833A1 · Kwon et al. · 2015 [cited by applicant]
US 20150159084A1 · Cho et al. · 2015 [cited by applicant]
US 20160336518A1 · Chun et al. · 2016 [cited by applicant]
US 20170117485A1 · Cho et al. · 2017 [cited by applicant]
US 20170148998A1 · Kang · 2017 [cited by examiner]
US 20210013411A1 · Mo et al. · 2021 [cited by applicant]
US 20210328155A1 · Cho et al. · 2021 [cited by applicant]
JP 2014522401A · 2014 [cited by applicant]
JP 2015530732A · 2015 [cited by applicant]
JP 2017510071A · 2017 [cited by applicant]
JP 2017518974A · 2017 [cited by applicant]
JP 2021521145A · 2021 [cited by applicant]
KR 1020100023783A · 2010 [cited by applicant]
KR 1020120021203A · 2012 [cited by applicant]
KR 1020150027937A · 2015 [cited by applicant]
KR 1020150108330A · 2015 [cited by applicant]
KR 1020150135109A · 2015 [cited by applicant]
KR 1020160022764A · 2016 [cited by applicant]
KR 1020180053121A · 2018 [cited by applicant]
KR 1020180125369A · 2018 [cited by applicant]
WO 2012165844A1 · 2012 [cited by applicant]
WO WO2015093878A1 · 2015 [cited by examiner]
WO 2019203550A1 · 2019 [cited by applicant]
WO WO2020175948A1 · 2020 [cited by examiner]
WO WO2020185059A1 · 2020 [cited by examiner]
WO-2020175948-A1 machine translation (Year: 2020). [cited by examiner]
WO 2020185059 A1 machine translation (Year: 2020). [cited by examiner]