IP Library Granted Patent US 9,859,507
Granted Patent B2
US 9,859,507 · App. 15/306,123 · Granted Jan 2, 2018

Organic electroluminescent compound and organic electroluminescent device comprising the same

Inventors: Hee-Ryong Kang (Seoul, KR); Hyun-Ju Kang (Gwangmyeong, KR); Young-Mook Lim (Cheonan, KR); Mi-Ja Lee (Cheonan, KR); Nam-Kyun Kim (Yongin, KR); Bitnari Kim (Cheonan, KR); Jin-Ri Hong (Cheonan, KR); Doo-Hyeon Moon (Hwaseong, KR); Su-Hyun Lee (Suwon, KR)
Assignee: ROHM AND HAAS ELECTRONIC MATERIALS KOREA LTD.
H01L51/0072C07D471/16C07D487/16C07D519/00C09K11/025C09K11/06C09K2211/1007C09K2211/1029C09K2211/1033C09K2211/1037C09K2211/1044C09K2211/1059C09K2211/1088C09K2211/1092H01L51/5016
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Quick Facts
Patent No.
US 9,859,507
App. No.
15/306,123
Granted
Jan 2, 2018
Kind
B2
Abstract

The present disclosure relates to an organic electroluminescent compound of Formula 1 (variables R1-R10 defined herein), and an organic electroluminescent device comprising the same. By using the organic electroluminescent compound according to the present disclosure, it is possible to produce an organic electroluminescent device which can be operated at a lowered driving voltage, shows excellence in luminous efficiency such as current efficiency and power efficiency, and has high color purity and improved lifespan.

Claims (21)

1. An organic electroluminescent compound represented by the following formula 1:

wherein

X and Y, each independently, represent —CR 12 — or —N—, with the proviso that X and Y are not be simultaneously —CR 12 —, and

R 1 to R 12 , each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted 3- to 30-memberedheteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, a substituted or unsubstituted mono- or di-(C1-C30)alkylamino, a substituted or unsubstituted mono- or di-(C6-C30)arylamino, or a substituted or unsubstituted (C1-C30)alkyl(C6-C30)arylamino; or may be linked to an adjacent substituent(s) to form a substituted or unsubstituted benzene ring or a substituted or unsubstituted naphthalene ring,

wherein the heteroaryl of the substituted or unsubstituted 3- to 30-memberedheteroaryl contains one or more hetero atoms selected from the group consisting of N, O and S.

2. The organic electroluminescent compound according to claim 1 , wherein the substituents of the substituted alkyl, the substituted aryl, the substituted heteroaryl, the substituted cycloalkyl, the substituted alkoxy, the substituted trialkylsilyl, the substituted dialkylarylsilyl, the substituted alkyldiarylsilyl, the substituted triarylsilyl, the substituted mono- or di-alkylamino, the substituted mono- or di-arylamino, the substituted alkylarylamino, and the substituted benzene ring or naphthalene ring in R 1 to R 12 , each independently, are at least one selected from the group consisting of deuterium, a halogen, a cyano, a carboxy, a nitro, a hydroxy, a (C1-C30)alkyl, a halo(C1-C30)alkyl, a (C1-C30)alkoxy, a (C1-C30)alkylthio, a (C3-C30)cycloalkyl, a 3- to 7-membered heterocycloalkyl, a (C6-C30)aryloxy, a (C6-C30)arylthio, a 3- to 30-membered heteroaryl unsubstituted or substituted with a (C6-C30)aryl or a di(C6-C30)arylamino, a (C6-C30)aryl unsubstituted or substituted with a 3- to 30-membered heteroaryl or a di(C6-C30)arylamino, atri(C1-C30)alkylsilyl, a tri(C6-C30)arylsilyl, a di(C1-C30)alkyl(C6-C30)arylsilyl, a (C1-C30)alkyldi(C6-C30)arylsilyl, an amino, a mono- or di-(C1-C30)alkylamino, a mono- or di-(C6-C30)arylamino, a (C1-C30)alkyl(C6-C30)arylamino, a (C1-C30)alkylcarbonyl, a (C1-C30)alkoxycarbonyl, a (C6-C30)arylcarbonyl, a di(C6-C30)arylboronyl, a di(C1-C30)alkylboronyl, a (C1-C30)alkyl(C6-C30)arylboronyl, a (C6-C30)aryl(C1-C30)alkyl, and a (C1-C30)alkyl(C6-C30)aryl.

3. The organic electroluminescent compound according to claim 1 , wherein the compound of formula 1 is represented by any one of the following formulae 2 to 4:

wherein R 1 to R 12 are as defined in claim 1 .

4. The organic electroluminescent compound according to claim 1 , wherein R 1 to R 12 , each independently, represent hydrogen, a substituted or unsubstituted (C1-C20)alkyl, a substituted or unsubstituted (C6-C20)aryl, a substituted or unsubstituted 5- to 30-membered heteroaryl, or a substituted or unsubstituted di(C6-C20)arylamino, or may be linked to an adjacent substituent(s) to form a substituted or unsubstituted benzenering or a substituted or unsubstituted naphthalene ring.

5. The organic electroluminescent compound according to claim 4 , wherein R 1 to R 12 , each independently, represent hydrogen, a substituted or unsubstituted (C1-C20)alkyl, or any one of the following formulae 5-1 to 5-9, or may be linked to an adjacent substituent(s) to form a substituted or unsubstituted benzene ring or a substituted or unsubstituted naphthalene ring:

wherein

L a , L b , L c , and L d , each independently, represent a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted 3- to 30-membered heteroarylene;

Z represents —S—, —O—, —NR 13 —, or —CR 14 R 15 —;

R 13 to R 15 , each independently, represent hydrogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted 3- to 30-membered heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, or a substituted or unsubstituted 3- to 7-membered heterocycloalkyl;

R 31 to R 37 , each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C3-C30)cycloalkenyl, a substituted or unsubstituted 3- to 7-membered heterocycloalkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted 3- to 30-membered heteroaryl, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a mono- or di-(C1-C30)alkylamino, a mono- or di-(C6-C30)arylamino, or a (C1-C30)alkyl(C6-C30)arylamino; or may be linked to an adjacent substituent(s) to form a substituted or unsubstituted, 3- to 30-membered, mono- or polycyclic, alicyclic or aromatic ring, whose carbon atom(s) may be replaced with at least one hetero atom selected from the group consisting of nitrogen, oxygen and sulfur;

a represents an integer of 1 to 3; b to d and f, each independently, represent an integer of 1 to 4; e represents an integer of 1 to 5; where a, b, c, d, e, or f is an integer of 2 or more, each of R 31 , R 32 , R 33 , R 34 , R 35 , or R 36 may be the same or different; and

* represents a bonding site;

wherein the heteroaryl(ene) and heterocycloalkyl, each independently, contain at least one hetero atom(s) selected from the group consisting of N, O and S.

6. The organic electroluminescent compound according to claim 5 , wherein at least one of R 1 to R 7 represents any one of formulae 5-6 to 5-8, and Z of formula 5-6 represents —NR 13 —.

7. The organic electroluminescent compound according to claim 1 , wherein the compound is selected from the group consisting of:

8. An organic electroluminescent device comprising the organic electroluminescent compound according to claim 1 .

Assignments (2)
CHANGE OF NAME Recorded Oct 17, 2024
From: ROHM & HAAS ELECTRONIC MATERIALS KOREA LTD
To: DUPONT SPECIALTY MATERIALS KOREA LTD
Reel/Frame 069185/0438 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 16, 2017
From: KANG, HEE-RYONG; KANG, HYUN-JU; LIM, YOUNG-MOOK; KIM, MI-JA; KIM, NAM-KYUN; KIM, BIT-NA-RI; HONG, JIN RI; MOON, DOO-HYEON; LEE, SU-HYUN
To: ROHM AND HAAS ELECTRONIC MATERIALS KOREA LTD.
Reel/Frame 044150/0447 →
Priority Claims (3)
KR 10-2014-0053261 · May 2, 2014 · national
KR 10-2014-0117823 · Sep 4, 2014 · national
KR 10-2015-0057081 · Apr 23, 2015 · national
Continuity (1)
Related Publication 20170047528A1 · Feb 16, 2017