IP Library Granted Patent US 8,946,984
Granted Patent B2
US 8,946,984 · App. 14/252,870 · Granted Feb 3, 2015

Electroluminescent device

Inventors: Junichi Tanabe (Takarazuka, JP); Hidetaka Oka (Takarazuka, JP); Hiroshi Yamamoto (Takarazuka, JP)
Assignee: BASF SE
H01L51/0052C07D307/91C07D405/14C07D409/14C09K11/06H01L51/0058H01L51/0072H01L51/0073H05B33/14H01L51/006H01L51/0061C09K2211/1022C09K2211/1088H01L51/0054Y02E10/549Y10S428/917
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Quick Facts
Patent No.
US 8,946,984
App. No.
14/252,870
Granted
Feb 3, 2015
Kind
B2
Abstract

Disclosed are electroluminescent devices that comprise organic layers that contain dibenzofuran compounds. The compounds are suitable components of, for example, blue-emitting, durable, organo-electroluminescent layers. The electroluminescent devices may be employed for full color display panels in, for example, mobile phones, televisions and personal computer screens.

Claims (36)

1. An electroluminescent device, comprising in the light emitting layer a compound of the formula

and a phosphorescent metal complex of Ir, Pt, Eu, Ru, Rh, Pd, Ag, Re, Os and Au as dopant, wherein R 81 and R 88 are independently of each other H, —OR 201 , —SR 202 and/or —NR 203 R 204 , C 1 -C 24 alkyl; C 1 -C 24 alkyl, which is substituted by E and/or interrupted by D; C 2 -C 18 alkenyl, C 2 -C 18 alkenyl, which is substituted by E, C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl, which is substituted by G, aryl, aryl, which is substituted by G, heteroaryl, or heteroaryl, which is substituted by G, silyl, SiR 62 R 63 R 64 , —CN, cyclic ether, —B(OR 65 ) 2 and/or halogen, wherein

R 201 is hydrogen, C 1 -C 24 alkyl, C 1 -C 24 alkyl, which is substituted by E and/or interrupted by D; C 2 -C 12 alkenyl, C 3 -C 6 alkenoyl, C 3 -C 8 cycloalkyl, or benzoyl, each of which may optionally be substituted by one or more groups C 1 -C 6 alkyl, halogen, —OH and/or C 1 -C 4 alkoxy; phenyl, naphthyl, phenanthryl, anthranyl, or pyrenyl, each of which may optionally be substituted by halogen, —OH, C 1 -C 12 alkyl, C 1 -C 12 alkoxy, phenoxy, C 1 -C 12 alkylsulfanyl, phenylsulfanyl, —N(C 1 -C 12 alkyl) 2 and/or diphenylamino;

R 202 is C 1 -C 24 alkyl, C 1 -C 24 alkyl, which is substituted by E and/or interrupted by D; C 2 -C 12 alkenyl, C 1 -C 8 alkanoyl, C 2 -C 12 alkenyl, C 3 -C 6 alkenoyl; C 3 -C 8 cycloalkyl, or benzoyl, each of which may optionally be substituted by one or more groups C 1 -C 6 alkyl, halogen, —OH, C 1 -C 4 alkoxy or C 1 -C 4 alkylsulfanyl; phenyl, naphthyl, phenanthryl, anthranyl, or pyrenyl, each of which may optionally be substituted by halogen, C 1 -C 12 alkyl, C 1 -C 12 alkoxy, phenyl-C 1 -C 3 alkyloxy, phenoxy, C 1 -C 12 alkylsulfanyl, phenylsulfanyl, —N(C 1 -C 12 alkyl) 2 , diphenylamino, —(CO)O(C 1 -C 8 alkyl), —(CO)—C 1 -C 8 alkyl, or (CO)N(C 1 -C 8 alkyl) 2 ;

R 203 and R 204 are independently of each other hydrogen, C 1 -C 24 alkyl, C 1 -C 24 alkyl, which is substituted by E and/or interrupted by D; C 2 -C 2 alkenyl, C 3 -C 8 cycloalkyl, or benzoyl, each of which may optionally be substituted by one or more groups C 1 -C 6 alkyl, halogen, —OH, or C 1 -C 4 alkoxy; phenyl-C 1 -C 3 alkyl, C 1 -C 8 alkanoyl, C 3 -C 12 alkenoyl; phenyl naphthyl, phenanthryl, anthranyl, or pyrenyl, each of which is optionally substituted by C 1 -C 12 alkyl, benzoyl or C 1 -C 12 alkoxy; or R 203 and R 204 together are C 2 -C 8 alkylene, or branched C 2 -C 8 alkylene optionally interrupted by —O—, —S—, or —NR 205 — and/or optionally substituted by hydroxyl, C 1 -C 4 alkoxy, C 2 -C 4 alkanoyloxy, or benzoyloxy, wherein the ring formed by R 203 and R 204 can optionally be condensed one or two times by phenyl which can be substituted one to three times with C 1 -C 8 -alkyl, C 1 -C 8 -alkoxy, halogen, or cyano;

R 205 is hydrogen, C 1 -C 24 alkyl, C 1 -C 24 alkyl, which is substituted by E and/or interrupted by D; C 2 -C 5 alkenyl, C 3 -C 8 cycloalkyl, phenyl-C 1 -C 3 alkyl, C 1 -C 8 alkanoyl, C 3 -C 12 alkenoyl; benzoyl; phenyl, naphthyl, phenanthryl, anthranyl, or pyrenyl, each of which is optionally substituted by C 1 -C 12 alkyl, benzoyl, or C 1 -C 12 alkoxy;

D is —CO—, —COO—, —OCOO—, —S—, —SO—, —SO 2 —, —O—, —NR 5 —, —SiR 61 R 62 —, —POR 5 —, —CR 63 ═CR 64 —, or —C≡—;

E is halogen, C 6 -C 14 aryl, which may be substituted by —OR 5 , —SR 5 , —NR 5 R 6 , SiR 62′ R 63′ R 64′ , wherein R 62′ , R 63′ and R 64′ are independently of each other a C 1 -C 8 alkyl group, a C 6 -C 24 aryl group or a C 7 -C 12 aralkyl group, —CN, cyclic ether and/or —B(OR 65 ) 2 , wherein R 65 is hydrogen, C 1 -C 24 alkyl, C 3 -C 8 cycloalkyl, C 7 -C 24 aralkyl, C 2 -C 18 alkenyl, C 2 -C 24 alkynyl, hydroxy, mercapto, C 1 -C 24 alkoxy, C 1 -C 24 alkylthio, C 6 -C 30 aryl, C 2 -C 30 heteroaryl, halogen, haloalkane, silyl, siloxanyl, and an alicyclic ring formed with adjacent substituents R 65 ; —OR 5 , —SR 5 , —NR 5 R 6 , —COR 8 , —COOR 7 , —CONR 5 R 6 , —CN, halogen, silyl, C 1 -C 18 alkyl, or heteroaryl,

G is E, or C 1 -C 18 alkyl, wherein R 5 and R 6 are independently of each other H, C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by C 1 -C 18 alkyl, C 1 -C 18 alkoxy, or silyl; C 1 -C 18 alkyl or C 1 -C 18 alkyl which is interrupted by —O—; or

R 5 and R 6 together form a five or six membered ring,

R 7 is H, C 6 -C 18 aryl, C 7 -C 12 alkylaryl, which are optionally substituted by C 1 -C 18 alkyl, or C 1 -C 18 alkoxy; C 1 -C 18 alkyl; or C 1 -C 18 alkyl which is interrupted by —O—;

R 8 is C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by C 1 -C 18 alkyl, or C 1 -C 18 alkoxy; C 1 -C 18 alkyl, C 7 -C 12 alkylaryl, or C 1 -C 18 alkyl which is interrupted by —O—;

R 61 and R 62 are independently of each other C 6 -C 18 aryl; C 6-18 aryl which is substituted by C 1 -C 18 alkyl, C 1 -C 18 alkoxy; or C 1 -C 18 alkyl which is interrupted by —O—,

R 63 and R 64 are independently of each other H, C 6 -C 18 aryl; C 6-18 aryl which is substituted by C 1 -C 18 alkyl, C 1 -C 18 alkoxy; or C 1 -C 18 alkyl which is interrupted by —O—,

wherein

R 82 , R 83 , R 86 and R 87 are independently of each other a group of the formula —(W 1 ) a —(W 2 ) b —W 3 ,

a and b are 0, or 1,

W 1 and W 2 are independently of each other a group of formula

and

R 11 , R 11′ , R 12 , R 12′ , R 13 , R 13′ , R 15 , R 15′ , R 16 , R 16′ , R 17 and R 17′ are independently of each other H, E, tri(C 1 -C 8 alkyl)silyl, C 6 -C 18 aryl; C 6 -C 18 aryl which is substituted by G; C 1 -C 18 alkyl; C 1 -C 18 alkyl which is substituted by E and/or interrupted by D; C 1 -C 18 alkoxy; or C 1 -C 18 alkoxy which is substituted by E and/or interrupted by D; C 7 -C 18 aralkyl; or C 7 -C 18 aralkyl which is substituted by G;

R 18 and R 19 are independently of each other C 1 -C 18 alkyl; C 1 -C 18 alkoxy, C 6 -C 18 aryl; C 7 -C 18 aralkyl; or R 18 and R 19 together form a ring, which can optionally be substituted by C 1 -C 8 alkyl,

W 3 is a group of formula —NR 70 R 71 , wherein R 70 and R 71 are independently of each other a group of formula

wherein R 72 , R 73 and R 74 are independently of each other hydrogen, C 1 -C 8 alkyl, a hydroxyl group, a mercapto group, C 1 -C 8 alkoxy, C 1 -C 8 alkylthio, halogen, halo-C 1 -C 8 alkyl, a cyano group, an aldehyde group, a ketone group, a carboxyl group, an ester group, a carbamoyl group, an amino group, a nitro group, a silyl group or a siloxanyl group, or R 70 and R 71 together with the nitrogen atom to which they are bonded form a five or six membered heterocyclic ring, which can be condensed by one or two optionally substituted phenyl groups; with the proviso that b is 1, if R 70 and R 71 are independently of each other a group of formula

2. The electroluminescent device according to claim 1 , wherein the light emitting layer comprises a compound of formula

wherein R 81 , R 83 , R 86 and R 88 are as defined in claim 1 .

3. The electroluminescent device according to claim 1 , wherein the light emitting layer comprises a compound of formula

wherein

R 81 and R 83 are independently of each other H, or NR 203 R 204 ,

R 203 and R 204 together form a five membered ring, wherein the ring formed by R 203 and R 204 can optionally be condensed one or two times by phenyl;

R 86 and R 88 are independently of each other a group of the formula —(W 1 ) a —(W 2 ) b —W 3 ,

a and b are 0, or 1,

W 1 and W 2 are independently of each other a group of formula

R 11 , R 11′ , R 12 and R 12′ R are H; and

W 3 is a group of formula —NR 70 R 71 , wherein R 70 and R 71 together with the nitrogen atom to which they are bonded form a five or six membered heterocyclic ring, which can be condensed by one or two optionally substituted phenyl groups.

4. The electroluminescent device according to claim 1 , wherein the compound of formula (Ia) is a compound of formula

5. A method of forming a light emitting layer of an electroluminescent device by incorporating the compounds of formula (Ia), (Ib), or (Ic) according to claim 1 with phosphorescent metal complexes of Ir, Pt, Eu, Ru, Rh, Pd, Ag, Re, Os and Au as a dopant therein.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT APPL. NO. 14/901,736 PREVIOUSLY RECORDED AT REEL: 039460 FRAME: 0615. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 8, 2017
From: BASF SE
To: UDC IRELAND LIMITED
Reel/Frame 042740/0222 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 25, 2016
From: BASF SE
To: UDC IRELAND LIMITED
Reel/Frame 039460/0615 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 20, 2014
From: TANABE, JUNICHI; OKA, HIDETAKA; YAMAMOTO, HIROSHI
To: BASF SE
Reel/Frame 032927/0675 →
Priority Claims (2)
EP 05104599 · May 30, 2005 · regional
EP 05107908 · Aug 30, 2005 · regional
Continuity (3)
Division 13164016 · Jun 20, 2011
Division 11921050
Related Publication 20140217335A1 · Aug 7, 2014