IP Library › Granted Patent US 12,501,829
Granted Patent B2
US 12,501,829 · App. 17/515,850 · Granted Dec 16, 2025

Compound for organic optoelectronic device, composition for organic optoelectronic device, organic optoelectronic device, and display device

Inventors: Hanill Lee (Suwon-si, KR); Wook Kim (Suwon-si, KR); Hyung Sun Kim (Suwon-si, KR); Eunhye An (Suwon-si, KR); Jiah Yoon (Suwon-si, KR); Sung-Hyun Jung (Suwon-si, KR); Jongwoo Choi (Suwon-si, KR)
Assignee: SAMSUNG SDI CO., LTD.
H10K85/6572C07D209/86C07D487/04C09K11/06H10K85/654H10K85/6574C09K2211/1018H10K50/11H10K2101/10
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,501,829
App. No.
17/515,850
Granted
Dec 16, 2025
Kind
B2
Abstract

A compound for an organic optoelectronic device, a composition for an organic optoelectronic device including the same, an organic optoelectronic device, and a display device, the compound being represented by a combination of Chemical Formula 1 and Chemical Formula 2,

Claims (34)

1 . An organic optoelectronic device, comprising:

an anode and a cathode facing each other, and

at least one organic layer between the anode and the cathode,

wherein:

the at least one organic layer includes a composition including a first compound and a second compound,

the first compound is represented by a combination of Chemical Formula 1 and Chemical Formula 2-1-i or Chemical Formula 2-1-ii,

in Chemical Formulae 1, 2-1-i, and 2-1-ii,

Ar is a substituted or unsubstituted C12 to C30 aryl group,

a1* and a2* are linking carbons, linked at * of Chemical Formula 2-1-i or at * of Chemical Formula 2-1-ii,

a3* and a4* are each independently C—R a ,

R a and R 1 to R 13 are each independently hydrogen, deuterium, a cyano group, a halogen, a substituted or unsubstituted C1 to C20 alkyl group, or a substituted or unsubstituted C6 to C20 aryl group,

R 14 is a substituted or unsubstituted C6 to C20 aryl group, and

the second compound is represented by Chemical Formula 3,

in Chemical Formula 3,

Y 1 and Y 2 are each independently a substituted or unsubstituted C6 to C20 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,

L 1 and L 2 are each independently a single bond or a substituted or unsubstituted C6 to C20 arylene group,

R b and R 15 to R 24 are each independently hydrogen, deuterium, a cyano group, a halogen, a substituted or unsubstituted amino group, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heterocyclic group, and

m is an integer of 0 to 2,

and a ratio of the first compound to the second compound is 3:7 to 6:4.

2 . The organic optoelectronic device as claimed in claim 1 , wherein Ar is a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, a substituted or unsubstituted phenanthrenyl group, or a substituted or unsubstituted triphenylene group.

3 . The organic optoelectronic device as claimed in claim 1 , wherein:

Ar is a group of Group I:

in Group I, * is a linking point.

4 . The organic optoelectronic device as claimed in claim 1 , wherein R 14 is a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, or a substituted or unsubstituted naphthyl group.

5 . The organic optoelectronic device as claimed in claim 1 , wherein R 9 to R 13 are each independently hydrogen, deuterium, a substituted or unsubstituted phenyl group, or a substituted or unsubstituted biphenyl group.

6 . The organic optoelectronic device as claimed in claim 1 , wherein the compound is a compound of Group 1:

7 . The organic optoelectronic device as claimed in claim 1 , wherein:

Chemical Formula 3 is represented by Chemical Formula 3-8;

in Chemical Formula 3-8,

R 15 to R 24 are each independently hydrogen or a substituted or unsubstituted C6 to C12 aryl group, and

moieties *-L 1 -Y 1 and *-L 2 -Y 2 are each independently a moiety of Group II,

in Group II, * is a linking point.

8 . A display device comprising the organic optoelectronic device as claimed in claim 1 .

9 . A display device comprising the organic optoelectronic device as claimed in claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2021
From: LEE, HANILL; KIM, WOOK; KIM, HYUNG SUN; AN, EUNHYE; YOON, JIAH; JUNG, SUNG-HYUN; CHOI, JONGWOO
To: SAMSUNG SDI CO., LTD.
Reel/Frame 057982/0337 →
Priority Claims (2)
KR 10-2020-0146197 · Nov 4, 2020 · national
KR 10-2021-0148039 · Nov 1, 2021 · national
Continuity (1)
Related Publication 20220140257A1 · May 5, 2022
References Cited (76)
US 5061569A · Vanslyke et al. · 1991 [cited by applicant]
US 5837166A · Kawamura et al. · 1998 [cited by applicant]
US 10897016B2 · Ma et al. · 2021 [cited by applicant]
US 20150041785A1 · Sannomiya et al. · 2015 [cited by applicant]
US 20150115240A1 · Fukumatsu et al. · 2015 [cited by applicant]
US 20150171340A1 · Lee · 2015 [cited by examiner]
US 20170069849A1 · Lee · 2017 [cited by examiner]
US 20170237017A1 · Parham · 2017 [cited by examiner]
US 20170305854A1 · Lee et al. · 2017 [cited by applicant]
US 20190214571A1 · Huh et al. · 2019 [cited by applicant]
US 20200176688A1 · Cho · 2020 [cited by examiner]
US 20200203631A1 · Gao et al. · 2020 [cited by applicant]
US 20210104698A1 · Kim et al. · 2021 [cited by applicant]
US 20210122765A1 · Wolohan et al. · 2021 [cited by applicant]
US 20220006022A1 · Suh · 2022 [cited by examiner]
US 20220310936A1 · Suh · 2022 [cited by examiner]
US 20220416177A1 · Hayashi · 2022 [cited by examiner]
US 20230019297A1 · Kim et al. · 2023 [cited by applicant]
US 20230131577A1 · Hayashi · 2023 [cited by examiner]
US 20230172065A1 · Park et al. · 2023 [cited by applicant]
US 20230247902A1 · No et al. · 2023 [cited by applicant]
US 20230263054A1 · Hwang · 2023 [cited by examiner]
CN 110746409A · 2020 [cited by applicant]
CN 110785863A · 2020 [cited by applicant]
CN 112996793A · 2021 [cited by applicant]
CN 113004287A · 2021 [cited by applicant]
CN 113004289A · 2021 [cited by applicant]
CN 114105992A · 2022 [cited by applicant]
CN 114163424A · 2022 [cited by applicant]
CN 114456172A · 2022 [cited by applicant]
CN 115669281A · 2023 [cited by applicant]
EP 2947071A1 · 2015 [cited by applicant]
EP 3034581A1 · 2016 [cited by applicant]
EP 4254528A1 · 2023 [cited by applicant]
EP 4349812A1 · 2024 [cited by applicant]
JP 1993009471A · 1993 [cited by applicant]
JP 1995126615A · 1995 [cited by applicant]
JP 1998095973A · 1998 [cited by applicant]
JP 6091428B2 · 2017 [cited by applicant]
JP 2022189759A · 2022 [cited by applicant]
JP 2023534166A · 2023 [cited by applicant]
JP 2023537660A · 2023 [cited by applicant]
KR 1020140143397A · 2014 [cited by applicant]
KR 1020170107919A · 2017 [cited by applicant]
KR 101818579B1 · 2018 [cited by applicant]
KR 1020180124766A · 2018 [cited by applicant]
KR 1020180137772A · 2018 [cited by applicant]
KR 1020190000597A · 2019 [cited by applicant]
KR 1020190001357A · 2019 [cited by applicant]
KR 1020190002206A · 2019 [cited by applicant]
KR 101959821B1 · 2019 [cited by applicant]
KR 1020190090204A · 2019 [cited by applicant]
KR 102031300B1 · 2019 [cited by applicant]
KR 102045766B1 · 2019 [cited by applicant]
KR 102054806B1 · 2019 [cited by applicant]
KR 102069310B1 · 2020 [cited by applicant]
KR 1020200018760A · 2020 [cited by applicant]
KR 1020200046750A · 2020 [cited by applicant]
KR 102193015B1 · 2020 [cited by applicant]
KR 1020210041166A · 2021 [cited by applicant]
KR 1020220017374A · 2022 [cited by applicant]
WO WO1995009147A1 · 1995 [cited by applicant]
WO WO2013088973A1 · 2013 [cited by applicant]
WO WO2013133219A1 · 2013 [cited by applicant]
WO WO2013133223A1 · 2013 [cited by applicant]
WO WO2016064227A1 · 2016 [cited by applicant]
WO WO2016194604A1 · 2016 [cited by applicant]
WO WO2018095391A1 · 2018 [cited by applicant]
WO WO2018182259A1 · 2018 [cited by applicant]
WO WO2018236092A1 · 2018 [cited by examiner]
Chinese Office Action and Search Report dated May 18, 2023. [cited by applicant]
Korean Notice of Allowance dated Feb. 27, 2024. [cited by applicant]
International Search Report dated Oct. 18, 2022 received in co-pending related application, U.S. Appl. No. 18/561,095. [cited by applicant]
Japanese Office action dated Oct. 22, 2024. [cited by applicant]
Korean Office action dated Aug. 28, 2024, received in co-pending related application, U.S. Appl. No. 18/561,095. [cited by applicant]
European Search Report dated May 19, 2025. [cited by applicant]