IP Library › Granted Patent US 12,453,284
Granted Patent B2
US 12,453,284 · App. 17/607,120 · Granted Oct 21, 2025

Anthracene compound and organic light-emitting device comprising same

Inventors: Hoon Jun Kim (Daejeon, KR); Ji Young Choi (Daejeon, KR); Wanpyo Hong (Daejeon, KR); Woochul Lee (Daejeon, KR); Joo Ho Kim (Daejeon, KR)
Assignee: LG CHEM, LTD.
H10K85/6574C07D307/91H10K50/11H10K2101/10
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Quick Facts
Patent No.
US 12,453,284
App. No.
17/607,120
Granted
Oct 21, 2025
Kind
B2
Abstract

Provided is an anthracene compound of Chemical Formula 1: wherein, in Chemical Formula 1: D is deuterium; n1 is 8; n2 is 7; and L is a direct bond or a substituted or unsubstituted arylene group, and an organic light emitting device including the same. Including a compound of Chemical Formula 1 in an organic light emitting device can lower the driving voltage and enhance light efficiency. In addition, lifetime properties of the device can be enhanced by thermal stability of the compound. The compound of Chemical Formula 1 has an advantage in terms of production costs since the amount of deuterium source used in the preparation is reduced.

Claims (24)

1. An anthracene compound of Chemical Formula 1:

wherein, in Chemical Formula 1:

D is deuterium;

n1 is 8;

n2 is 7; and

L is a direct bond or any one selected from among the following structures:

wherein the structures can be unsubstituted or substituted with a substituent selected from the group consisting of deuterium, an alkyl group, an aryl group, and a heteroaryl group, or a substituent in which two or more of these substituents are linked together.

2. The anthracene compound of claim 1 , wherein Chemical Formula 1 is any one of the following Chemical Formulae 101 to 104:

wherein in Chemical Formulae 101 to 104:

D, n1, n2 and L have the same definitions as in Chemical Formula 1.

3. The anthracene compound of claim 1 , wherein Chemical Formula 1 is Chemical Formula 201 or 202:

wherein in Chemical Formula 201 or 202:

D, n1, n2 and L have the same definitions as in Chemical Formula 1.

4. The anthracene compound of claim 2 , wherein Chemical Formula 1 is Chemical Formula 101 or 102.

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

6. An organic light emitting device comprising:

a first electrode;

a second electrode provided opposite to the first electrode; and

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

wherein one or more layers of the organic material layers include the anthracene compound of claim 1 .

7. The organic light emitting device of claim 6 , wherein the organic material layer includes a light emitting layer, and the light emitting layer includes the anthracene compound as a host.

8. The organic light emitting device of claim 7 , wherein the light emitting layer further includes an arylamine-based compound.

9. The organic light emitting device of claim 7 , wherein the light emitting layer further includes a boron compound.

10. The organic light emitting device of claim 7 , wherein the light emitting layer further includes an arylamine-based compound comprising deuterium.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 28, 2021
From: KIM, HOON JUN; CHOI, JI YOUNG; HONG, WANPYO; LEE, WOOCHUL; KIM, JOO HO
To: LG CHEM, LTD.
Reel/Frame 057947/0860 →
Priority Claims (1)
KR 10-2019-0136733 · Oct 30, 2019 · national
Continuity (1)
Related Publication 20220165966A1 · May 26, 2022
References Cited (35)
US 8759818B2 · LeCloux et al. · 2014 [cited by applicant]
US 20020076576A1 · Li · 2002 [cited by examiner]
US 20080315754A1 · Kawamura · 2008 [cited by examiner]
US 20100045170A1 · Lee et al. · 2010 [cited by applicant]
US 20110121269A1 · Lecloux · 2011 [cited by examiner]
US 20150041773A1 · Park et al. · 2015 [cited by applicant]
US 20150144898A1 · Dai et al. · 2015 [cited by applicant]
US 20170018723A1 · Cha et al. · 2017 [cited by applicant]
US 20170025608A1 · Herron et al. · 2017 [cited by applicant]
US 20180013071A1 · Cha et al. · 2018 [cited by applicant]
US 20180182971A1 · Park et al. · 2018 [cited by applicant]
US 20190305227A1 · Yoon et al. · 2019 [cited by applicant]
US 20200013957A1 · Suh et al. · 2020 [cited by applicant]
US 20220384733A1 · Choi · 2022 [cited by examiner]
US 20230084250A1 · Lee · 2023 [cited by examiner]
EP 3524661A1 · 2019 [cited by applicant]
JP 2007077094A · 2007 [cited by examiner]
KR 100910150 · 2009 [cited by applicant]
KR 1020130022071 · 2013 [cited by applicant]
KR 1020150011347 · 2015 [cited by applicant]
KR 1020150018229 · 2015 [cited by applicant]
KR 1020160095827 · 2016 [cited by applicant]
KR 1020160112111 · 2016 [cited by applicant]
KR 1020170008673 · 2017 [cited by applicant]
KR 1020170009714 · 2017 [cited by applicant]
KR 1020170010724 · 2017 [cited by applicant]
KR 1020170039020 · 2017 [cited by applicant]
KR 1020180037717 · 2018 [cited by applicant]
KR 1020180068861 · 2018 [cited by applicant]
KR 1020190113498 · 2019 [cited by applicant]
WO 2018164511 · 2018 [cited by applicant]
Czerwieniec et al., “Blue-Light Emission of Cu(I) Complexes and Singlet Harvesting”, Inorganic Chemistry (2011) vol. 50, pp. 8293-8301. (Year: 2011). [cited by examiner]
Hirata et al., “Relationship between room temperature phosphorescence and deuteration position in a purely aromatic compound”, Chemical Physics Letters, 591 (2014) pp. 119-125. (Year: 2013). [cited by examiner]
Totani et al., machine translation of JP-2007077094-A (2007) pp. 1-38. (Year: 2007). [cited by examiner]
Tsuji et al., “The hydrogen/deuterium isotope effect of the host material on the lifetime of organic light-emitting diodes,” Chem. Commun. 50:14870-14872 (2014). [cited by applicant]