IP Library Granted Patent US 7,233,019
Granted Patent B2
US 7,233,019 · App. 10/831,845 · Granted Jun 19, 2007

Electroluminescent silylated pyrenes, and devices made with such compounds

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 7,233,019
App. No.
10/831,845
Granted
Jun 19, 2007
Kind
B2
Abstract

This invention relates to electroluminescent silylated pyrene compounds. It also relates to electronic devices in which the active layer includes an electroluminescent silylated pyrene compound.

Claims (16)

1. An organic electronic device comprising at least one active layer between two electrical contact layers, wherein the at least one active layer comprises a compound represented by Formula I

wherein:

R 1 –R 4 =H or an Si(R 5 ) 3 -substituted aryl group, wherein said Si(R 5 ) 3 -substituted aryl group is a substituted aryl group having at least one Si(R 5 ) 3 group as a substituent, provided any substituents other than Si(R 5 ) 3 groups are alkyl or aryl groups;

R 5 is C 1 –C 6 alkyl or silyl-substituted C 1 –C 6 alkyl, C 3 –C 6 cycloalkyl or silyl-substituted C 3 –C 6 cycloalkyl, or C 6 –C 10 aryl or silyl-substituted C 6 –C 10 aryl; and wherein at least one of R 1 –R 4 is an Si(R 5 ) 3 -substituted aryl group.

2. The organic electronic device of claim 1 , wherein the active layer is a light-emitting layer.

3. The organic electronic device of claim 1 , wherein the active layer is a charge transport layer.

4. The device of claim 1 , wherein each of R 1 –R 4 is an Si(R 5 ) 3 -substituted aryl group, and R 1 =R 2 =R 3 =R 4 .

5. The device of claim 4 , wherein the Si(R 5 ) 3 -substituted aryl group is a trimethylsilylphenyl group.

6. The device of claim 1 , wherein the at least one active layer further comprises a diluent selected from the group consisting of poly(N-vinyl carbazole), polysilane, 4,4′-N,N′-dicarbazole biphenyl, and tertiary amines.

7. The device of claim 1 , further comprising a hole transport layer comprising a hole transport material selected from the group consisting of: N,N′-diphenyl-N,N′-bis(3-methylphenyl)-[1,1′-biphenyl]-4,4′-diamine (TPD), 1,1-bis[(di-4-tolylamino)phenyl]cyclohexane (TAPC), N,N′-bis(4-methylpheny)-N,N′-bis(4-ethylphenyl)-[1,1′-(3,3′-dimethyl)biphenyl]-4,4′-diamine (ETPD), tetrakis-(3-methylphenyl)-N,N,N′,N′-2,5-phenylenediamine (PDA), α-phenyl-4-N,N-diphenylaminostyrene (TPS), p-(diethylamino)benzaldehyde diphenylhydrazone (DEH), triphenylamine (TPA), bis[4-(N,N-diethylamino)-2-methylphenyl](4-methylphenyl)methane (MPMP), 1-phenyl-3-[p-(diethylamino)styryl]-5-[p-(diethylamino)phenyl]pyrazoline (PPR or DEASP), 1,2-trans-bis(9H-carbazol-9-yl)cyclobutane (DCZB), N,N,N′,N′-tetrakis(4-methylphenyl)-(1,1′-biphenyl)-4,4′-diamine (TTB), 4,4′-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (NPB or NPD), carbazole biphenyl (CBP), polymeric polypyrroles and polythiophenes, porphyrinic compounds, and combinations thereof.

8. The device of claim 1 , further comprising an electron transport layer comprising an electron transport material selected from the group consisting of tris(8-hydroxyquinolato)aluminum (Alq3); 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (DDPA); 4,7-diphenyl-1,10-phenanthroline (DPA); 2-(4-biphenylyl)-5-(4-t-butylphenyl)-1,3,4-oxadiazole (PBD); 3-(4-biphenylyl)-4-phenyl-5-(4-t-butylphenyl)-1,2,4-triazole (TAZ) and combinations thereof.

9. A compound represented by Formula I

wherein:

R 1 –R 4 =H or an Si(R 5 ) 3 -substituted aryl group, wherein said Si(R 5 ) 3 -substituted aryl group is a substituted aryl group having at least one Si(R 5 ) 3 group as a substituent, provided any substituents other than Si(R 5 ) 3 groups are alkyl or aryl groups;

R 5 is C 1 –C 6 alkyl or silyl-substituted C 1 –C 6 alkyl, C 3 –C 6 cycloalkyl or silyl-substituted C 3 –C 6 cycloalkyl, or C 6 –C 10 aryl or silyl-substituted C 6 –C 10 aryl; and wherein at least one of R 1 –R 4 is an Si(R 5 ) 3 -substituted aryl group.

10. The compound of claim 9 , wherein R 1 =R 2 =R 3 =R 4 =Si(R 5 ) 3 -substituted aryl group; R 5 is selected from the group of C 1 –C 6 alkyl and C 3 –C 6 cycloalkyl groups, and the compound is represented by Formula II or Formula III:

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2019
From: E. I. DU PONT DE NEMOURS AND COMPANY
To: LG CHEM, LTD.
Reel/Frame 050150/0482 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 4, 2004
From: IONKIN, ALEX SERGEY; WANG, YING
To: E. I. DU PONT DE NEMOURS AND COMPANY
Reel/Frame 014942/0249 →