Composition for organic optoelectric device and organic optoelectric device and display device

Patent metadata

Field	Value
Publication number	US-10600971-B2
Application number	US-201715644939-A
Country	US
Kind code	B2
Filing date	Jul 10, 2017
Priority date	Aug 11, 2016
Publication date	Mar 24, 2020
Grant date	Mar 24, 2020

Abstract

Disclosed are a composition for an organic optoelectric device including at least one of a first host compound represented by a combination of Chemical Formula 1 and Chemical Formula 2, and at least one of a second host compound represented by Chemical Formula 3, and an organic optoelectric device including the same, and a display device. Details of Chemical Formulae 1 to 3 are the same as described in the detailed description.

First claim

What is claimed is:

1. A composition for an organic optoelectric device, comprising:
at least one of a first host compound represented by a combination of Chemical Formula 1 and Chemical Formula 2, and
at least one of a second host compound represented by Chemical Formula 3:

wherein, in Chemical Formulae 1 to 3,
two adjacent *'s of Chemical Formula 1 are bound to two adjacent *'s of Chemical Formula 2 and the remainder *'s of Chemical Formula 1 not being bound to *'s of Chemical Formula 2 are CR a ,
R a and R 1 to R 6 are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C20 aryl group, or a combination thereof,
the substituent A is a substituted or unsubstituted carbazolyl group,
X is O or S,
Z 1 to Z 4 are independently N or C-L a -R b ,
at least two of Z 1 to Z 4 are N,
R b is a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted quaterphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted pyrimidinyl group, a substituted or unsubstituted triazinyl group, a substituted or unsubstituted pyrazinyl group, a substituted or unsubstituted pyridazinyl group, a substituted or unsubstituted quinolinyl group, a substituted or unsubstituted isoquinolinyl group, a substituted or unsubstituted quinazolinyl group, a substituted or unsubstituted benzofuran pyrimidinyl group, or a substituted or unsubstituted benzothiophene pyrimidinyl group,
Y is a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, a substituted or unsubstituted C6 to C20 arylamine group, or a combination thereof,
L a , L 1 , and L 2 are independently a single bond or a substituted or unsubstituted C6 to C30 arylene group, and
the “substituted” refers to replacement of at least one hydrogen by deuterium, a C1 to C4 alkyl group, a C6 to C20 arylamine group, a C6 to C12 aryl group, or a C2 to C20 heteroaryl group.

2. The composition for an organic optoelectric device as claimed in claim 1 , wherein Chemical Formula 1 is represented by Chemical Formula 1-I or Chemical Formula 1-II:

wherein, in Chemical Formula 1-I and Chemical Formula 1-II,
two adjacent *'s are bound to two adjacent *'s of Chemical Formula 2 and the remainder *'s not being bound to *'s of Chemical Formula 2 are CR a ,
L 1 is a single bond or a substituted or unsubstituted C6 to C30 arylene group,
Ar is a substituted or unsubstituted C6 to C30 aryl group, and
R a and R 7 to R 12 are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C20 aryl group, or a combination thereof.

3. The composition for an organic optoelectric device as claimed in claim 1 , wherein the first host compound is represented by one of Chemical Formula A, Chemical Formula B, Chemical Formula C, Chemical Formula D, Chemical Formula E, and Chemical Formula F:

wherein, in Chemical Formula A to Chemical Formula F,
the substituent A is a substituted or unsubstituted carbazolyl group,
Y is a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heterocyclic group,
L 1 and L 2 are independently a single bond or a substituted or unsubstituted C6 to C30 arylene group, and
R a1 to R a4 and R 1 to R 4 are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C20 aryl group, or a combination thereof.

4. The composition for an organic optoelectric device as claimed in claim 1 , wherein the first host compound is represented by one of Chemical Formula B1 to Chemical Formula B4, Chemical Formula C1 to Chemical Formula C4, Chemical Formula E1 to Chemical Formula E4, and Chemical Formula F1 to Chemical Formula F4:

wherein, in Chemical Formula B1 to Chemical Formula B4, Chemical Formula C1 to Chemical Formula C4, Chemical Formula E1 to Chemical Formula E4, and Chemical Formula F1 to Chemical Formula F4,
Ar is a substituted or unsubstituted C6 to C20 aryl group,
Y is a substituted or unsubstituted C6 to C20 aryl group, or a substituted or unsubstituted C2 to C20 heterocyclic group,
L 1 and L 2 are independently a single bond, or a substituted or unsubstituted C6 to C20 arylene group, and
R 1 to R 4 and R 7 to R 12 are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C20 aryl group, or a combination thereof.

5. The composition for an organic optoelectric device as claimed in claim 1 , wherein the L 1 is a single bond or selected from linking groups of Group I:

wherein, Group I, * is a linking point with an adjacent atom.

6. The composition for an organic optoelectric device as claimed in claim 1 , wherein the L 2 is a single bond or a substituted or unsubstituted phenylene group, and
the Y is a substituted or unsubstituted phenyl group, 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, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted diphenylamine group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, or a substituted or unsubstituted dibenzothiophenyl group.

7. The composition for an organic optoelectric device as claimed in claim 1 , wherein the L 1 and L 2 are independently a single bond, a substituted or unsubstituted phenylene group, or a substituted or unsubstituted biphenylene group,
the Y is a substituted or unsubstituted phenyl group, 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, a substituted or unsubstituted triphenylene group, or a substituted or unsubstituted fluorenyl group, and
the “sub

Assignees

• Samsung Sdi Co Ltd

Inventors

• Jang Chunkeun
• Yu Eun Sun
• Lee Sangshin
• Jung Sung-Hyun
• Jung Ho Kuk
• Kim Byungku
• Kim Changwoo
• Han Sujin

Classifications

• C09K2211/185

  of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd · CPC title

• C09K11/06 Primary

  containing organic luminescent materials · CPC title

• C07D487/04 Primary

  Ortho-condensed systems · CPC title

• C09K11/025

  non-luminescent particle coatings or suspension media · CPC title

• C09K2211/1007

  Non-condensed systems · CPC title