IP Library › Granted Patent US 11,629,126
Granted Patent B2
US 11,629,126 · App. 16/336,720 · Granted Apr 18, 2023

Materials for organic electroluminescent devices

Inventors: Katja Maria Scheible (Darmstadt, DE); Fabrice Eckes (Saint Louis, FR); Holger Heil (Frankfurt am Main, DE); Beate Burkhart (Darmstadt, DE); Dominik Joosten (Frankfurt am Main, DE); Elvira Montenegro (Weinheim, DE)
Assignee: MERCK PATENT GMBH
C07D209/82C07C211/61C07C305/06C07D307/91C07D333/76C07F7/0816H01L51/006H01L51/0058H01L51/0061H01L51/0072H01L51/0073H01L51/0074H01L51/0094C07C2602/06C07C2603/18C07C2603/26H01L51/0067H01L51/0085H01L51/50H01L51/506H01L51/5056Y02E10/549
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Quick Facts
Patent No.
US 11,629,126
App. No.
16/336,720
Granted
Apr 18, 2023
Kind
B2
Abstract

The present invention relates to compounds of formula (1). The compounds are suitable for use in electronic devices, in particular organic electroluminescent devices, comprising these compounds. In some embodiments, the compounds are used as matrix materials for phosphorescent or fluorescent emitters as well as a hole-blocking or electron-transport materials.

Claims (43)

1. A crosslinked compound obtained by crosslinking groups Q of a compound of the formula (2) or (3),

where

Ar 3 , Ar 4 , Ar 5 are selected on each occurrence, identically or differently, from the group consisting of an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R;

Q is on each occurrence, identically or differently, a crosslinkable group bonded to the adjacent phenyl group via a single bond, or Q is a crosslinkable mono- or polycyclic group condensed on the adjacent phenyl group;

R is on each occurrence, identically or differently, H, D, F, Cl, Br, I, CHO, N(Ar) 2 , C(═O)Ar, P(═O)(Ar) 2 , S(═O)Ar, S(═O) 2 Ar, (R)C═C(R)Ar, CN, NO 2 , Si(R 1 )3, B(OR 1 ) 2 , B(R 1 ) 2 , B(N(R 1 ) 2 ) 2 , OSO 2 R 1 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 C atoms or a straight-chain alkenyl or alkynyl group having 2 to 40 C atoms or a branched or cyclic alkyl, alkenyl, alkynyl, alkoxy or thioalkoxy group having 3 to 40 C atoms, each of which may be substituted by one or more radicals R 1 , where one or more, non-adjacent CH 2 groups may be replaced by (R 1 )C═C(R 1 ), C≡C, Si(R 1 ) 2 , Ge(R 1 ) 2 , Sn(R 1 ) 2 , C═O, C═S, C═Se, P(═O)(R 1 ), SO, SO 2 , N(R 1 ), O, S or CON(R 1 ) and where one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R 1 , or an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R 1 , where optionally two adjacent substituents R can form a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring system with one another;

Ar is an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R 1 ;

R 1 is on each occurrence, identically or differently, H, D, F, Cl, Br, I, CHO, N(R 2 ) 2 , C(═O)R 2 , P(═O)(R 2 ) 2 , S(═O)R 2 , S(═O) 2 R 2 , (R 2 )C═C(R 2 ) 2 , CN, NO 2 , Si(R 2 ) 3 , B(OR 2 ) 2 , B(R 2 ) 2 , B(N(R 2 ) 2 ) 2 , OSO 2 R 2 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 C atoms or a straight-chain alkenyl or alkynyl group having 2 to 40 C atoms or a branched or cyclic alkyl, alkenyl, alkynyl, alkoxy or thioalkoxy group having 3 to 40 C atoms, each of which may be substituted by one or more radicals R 2 , where one or more, non-adjacent CH 2 groups may be replaced by (R 2 )C═C(R 2 ), C≡C, Si(R 2 ) 2 , Ge(R 2 ) 2 , Sn(R 2 ) 2 , C═O, C═S, C═Se, P(═O)(R 2 ), SO, SO 2 , N(R 2 ), O, S or CON(R 2 ) and where one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R 2 , or an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R 2 , where optionally two adjacent substituents R 1 can form a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring system with one another;

R 2 is on each occurrence, identically or differently, H, D, F, Cl, Br, I, CHO, CN, NO 2 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 20 C atoms or a straightchain alkenyl or alkynyl group having 2 to 20 C atoms or a branched or cyclic alkyl, alkenyl, alkynyl, alkoxy or thioalkoxy group having 3 to 20 C atoms, or an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms or an aryloxy or heteroaryloxy group having 5 to 30 aromatic ring atoms; where optionally two adjacent substituents R 2 can form a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring system with one another;

m is on each occurrence, identically or differently, 1 or 2;

n is on each occurrence, identically or differently, 0 or 1;

with the proviso that m+n=2 in the amino moiety comprising a group Ar 3 and an aromatic or heteroaromatic ring system containing Y, and m+n=2 in the amino moiety comprising a group Ar 5 and an aromatic or heteroaromatic ring system containing Y;

p is 1;

s is on each occurrence, identically or differently, 0, 1, 2, 3 or 4; and

t is on each occurrence, identically or differently, 0, 1, 2 or 3.

2. The compound according to claim 1 ,

with the proviso that s≤3 and t≤2 when the corresponding phenyl ring is substituted by a group Q which corresponds to a mono- or polycyclic group condensed on this phenyl ring.

3. The compound according to claim 1 , characterized in that Q is on each occurrence, identically or differently, a crosslinkable group selected from terminal or cyclic alkenyl groups, terminal dienyl groups, terminal alkynyl groups, alkenyloxy groups, dienyloxy groups, alkynyloxy groups, acrylic acid derivatives, oxetane groups, oxirane groups, silanes groups and cyclobutane groups.

4. The compound according to claim 1 , characterized in that Q is selected from groups of the following formulae Q1 to Q24,

where the dashed bond in the formulae Q1 to Q11, Q13 to Q24 and the dashed bonds in the formula Q12 represent the linking of the crosslinkable group to; the adjacent phenyl group of the formula (2) or (3);

and where

R 11 , R 12 and R 13 are on each occurrence, identically or differently, H, a straight-chain or branched alkyl group having 1 to 6 C atoms;

Ar 10 is on each occurrence, in each case identically or differently, a mono- or polycyclic, aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R, where R is as defined in claim 1 ;

u is an integer from 0 to 8; and

v is an integer from 1 to 8.

5. The compound according to claim 1 , where Ar 3 , Ar 4 and Ar 5 are selected on each occurrence, identically or differently, from the group consisting of an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms, which may be substituted by one or more radicals R.

6. The compound according to claim 1 , where Ar 3 , Ar 4 and Ar 5 are selected on each occurrence, identically or differently, from the group consisting of benzene, naphthalene, anthracene, biphenyl, terphenyl, quaterphenyl, fluorene, dibenzofuran, dibenzothiophene, carbazole, indolocarbazole, indenocarbazole, pyridine, quinoline, isoquinoline, pyridazine, benzopyridazine, pyrimidine, benzopyrimidine, quinoxaline, pyrazine, azacarbazole, benzocarboline, 1,3,5-triazine, 1,2,4-triazine, 1,2,3-triazine, each of which may be substituted by one or more radicals R.

7. The compound according to claim 1 , where m is equal to 1 and n is equal to 1.

8. The compound according to claim 1 , where m is equal to 1.

9. A formulation comprising at least one compound according to claim 1 and at least one solvent.

10. An electronic device comprising at least one compound according to claim 1 selected from the group consisting of organic electroluminescent devices, organic integrated circuits, organic field-effect transistors, organic thin-film transistors, organic light-emitting transistors, organic solar cells, dye-sensitised organic solar cells, organic optical detectors, organic photoreceptors, organic field-quench devices, light-emitting electrochemical cells, organic laser diodes and organic plasmon emitting devices.

11. An organic electroluminescent device comprising a compound according to claim 1 wherein the compound is used in a hole-transport layer or in a hole-injection layer, where this layer may also be doped.

12. The compound according to claim 1 , where Ar 3 and Ar 5 are selected on each occurrence, identically or differently, from the groups of the following formulae (A-1) to (A-51),

where the dashed bond indicates the bond to the nitrogen atom,

where the groups of formulae (A-1) to (A-51) may further be substituted at each free position by a group R as defined in claim 1 , and where

R 0 , in formulae (A-18), (A-34) to (A-37), (A-44), (A-45) and (A-47), is selected on each occurrence, identically or differently, from the group consisting of H, D, F, CN, Si(R 3 ) 3 , a straight-chain alkyl group having 1 to 20 C atoms or a branched or cyclic alkyl group having 3 to 20 C atoms, each of which may be substituted by one or more radicals R 1 , an aromatic or heteroaromatic ring system having 5 to 18 aromatic ring atoms, which may in each case be substituted by one or more radicals R 1 , where two adjacent substituents R 0 may optionally form a mono- or polycyclic, aliphatic ring system or aromatic ring system, which may be substituted by one or more radicals R 1 .

13. The compound according to claim 12 , where Ar 4 is on each occurrence, identically or differently, selected from the groups of the following formulae (B-1) to (B-24),

where the dashed bonds in (B-1) to (B-24) indicate the bonds to the nitrogen atoms of the arylamino groups depicted in formula (2) or (3);

where the groups of formulae (B-1) to (B-24) may further be substituted at each free position by a group R, wherein

R is on each occurrence, identically or differently, H, D, F, Cl, Br, I, CHO, N(Ar) 2 , C(═O)Ar, P(═O)(Ar) 2 , S(═O)Ar, S(═O) 2 Ar, (R)C═C(R)Ar, CN, NO 2 , Si(R 1 ) 3 , B(OR 1 ) 2 , B(R 1 ) 2 , B(N(R 1 ) 2 ) 2 , OSO 2 R 1 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 C atoms or a straight-chain alkenyl or alkynyl group having 2 to 40 C atoms or a branched or cyclic alkyl, alkenyl, alkynyl, alkoxy or thioalkoxy group having 3 to 40 C atoms, each of which may be substituted by one or more radicals R 1 , where one or more, non-adjacent CH 2 groups may be replaced by (R 1 )C═C(R 1 ), C≡C, Si(R 1 ) 2 , Ge(R 1 ) 2 , Sn(R 1 ) 2 , C═O, C═S, C═Se, P(═O)(R 1 ), SO, SO 2 , N(R 1 ), O, S or CON(R 1 ) and where one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R 1 , or an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R 1 , where optionally two adjacent substituents R can form a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring system with one another;

Ar is an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R 1 ;

R 1 is on each occurrence, identically or differently, H, D, F, Cl, Br, I, CHO, N(R 2 ) 2 , C(═O)R 2 , P(═O)(R 2 ) 2 , S(═O)R 2 , S(═O) 2 R 2 , (R 2 )C═C(R 2 ) 2 , CN, NO 2 , Si(R 2 ) 3 , B(OR 2 ) 2 , B(R 2 ) 2 , B(N(R 2 ) 2 ) 2 , OSO 2 R 2 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 C atoms or a straight-chain alkenyl or alkynyl group having 2 to 40 C atoms or a branched or cyclic alkyl, alkenyl, alkynyl, alkoxy or thioalkoxy group having 3 to 40 C atoms, each of which may be substituted by one or more radicals R 2 , where one or more, non-adjacent CH 2 groups may be replaced by (R 2 )C═C(R 2 ), C≡C, Si(R 2 ) 2 , Ge(R 2 ) 2 , Sn(R 2 ) 2 , C═O, C═S, C═Se, P(═O)(R 2 ), SO, SO 2 , N(R 2 ), O, S or CON(R 2 ) and where one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R 2 , or an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R 2 , where optionally two adjacent substituents R 1 can form a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring system with one another;

R 2 is on each occurrence, identically or differently, H, D, F, Cl, Br, I, CHO, CN, NO 2 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 20 C atoms or a straight-chain alkenyl or alkynyl group having 2 to 20 C atoms or a branched or cyclic alkyl, alkenyl, alkynyl, alkoxy or thioalkoxy group having 3 to 20 C atoms, or an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms or an aryloxy or heteroaryloxy group having 5 to 30 aromatic ring atoms; where optionally two adjacent substituents R 2 can form a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring system with one another;

and where R 0 has the same meaning as in claim 12 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 26, 2019
From: ECKES, FABRICE; MONTENEGRO, ELVIRA; HEIL, HOLGER; JOOSTEN, DOMINIK; BURKHART, BEATE; SCHEIBLE, KATJA MARIA
To: MERCK PATENT GMBH
Reel/Frame 048703/0404 →
Priority Claims (1)
EP 16192507 · Oct 6, 2016 · regional
Continuity (1)
Related Publication 20190225581A1 · Jul 25, 2019