Materials for organic electroluminescent devices

Patent metadata

Field	Value
Publication number	US-9741942-B2
Application number	US-201314434460-A
Country	US
Kind code	B2
Filing date	Sep 13, 2013
Priority date	Oct 11, 2012
Publication date	Aug 22, 2017
Grant date	Aug 22, 2017

Abstract

The present invention relates to compounds according to formula (1), a method for producing these compounds and electronic devices, in particular organic electroluminescent devices containing said compounds.

First claim

The invention claimed is:

1. A compound of formula (1),

wherein:
X is on each occurrence, identically or differently, CR or N; or two adjacent groups X together stand for a group selected from NR, O or S, resulting in the formation of a five-membered ring;
Y is on each occurrence, identically or differently, Z═Z, O, S or NR, where R is not H;
Z is on each occurrence, identically or differently, CR or N or the adjacent groups Z═Z together stand for a group of formula (2),

where X has the meanings given above and the dashed bonds indicate the linking of this group;

L is not present for n=1 and is a single bond or a divalent group for n=2 and a trivalent group for n=3 and a tetravalent group for n=4 and a pentavalent group for n=5 and a hexavalent group for n=6; L here is bonded at any desired point of the basic structure instead of a group R;
R is selected on each occurrence, identically or differently, from the group consisting of H, D, F, Cl, Br, I, CN, NO 2 , N(Ar 1 ) 2 , N(R 1 ) 2 , C(═O)Ar 1 , C(═O)R 1 , P(═O)(Ar 1 ) 2 , a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 40 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 40 C atoms or an alkenyl or alkynyl group having 2 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═CR 1 , Si(R 1 ) 2 , C═O, C═S, C═NR 1 , P(═O)(R 1 ), SO, SO 2 , NR 1 , O, S or CONR 1 and where one or more H atoms optionally is replaced by D, F, Cl, Br, I, CN or NO 2 , an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which is optionally in each case substituted by one or more radicals R 1 , an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 1 , an aralkyl or heteroaralkyl group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 1 , or a combination of these systems, where two or more adjacent substituents R may optionally form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which is optionally substituted by one or more radicals R 1 ;
Ar 1 is on each occurrence, identically or differently, an aromatic or heteroaromatic ring system having 5-30 aromatic ring atoms, which is optionally substituted by one or more non-aromatic radicals R 1 ; two radicals Ar 1 here which are bonded to the same N atom or P atom may also be bridged to one another by a single bond or a bridge selected from N(R 1 ), C(R 1 ) 2 or O;
R 1 is selected from the group consisting of H, D, F, CN, an aliphatic hydrocarbon radical having 1 to 20 C atoms, an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms, in which one or more H atoms is optionally replaced by D, F, Cl, Br, I, CN or an alkyl group having 1 to 10 C atoms or an alkenyl group having 2 to 10 C atoms, where two or more adjacent substituents R 1 may form a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring system with one another;
n is 1, 2, 3, 4, 5 or 6;
where the following compound is excluded from the invention:

2. The compound according to claim 1 , selected from the compounds of formula (5) and formula (9),

where the radical R on the nitrogen in formula (9) is not equal to H.

3. The compound according to claim 1 , selected from compounds of formula (6),

where n=2 or 3.

4. The compound according to claim 1 , selected from compounds of formulae (7), (8), (10) and (11),

where n stands for 2 or 3, a maximum of one group X per ring stands for N and the other groups X stand for CR and the radical R on the nitrogen in formula (10) and (11) is not equal to H.

5. The compound according to claim 1 , selected from compounds of formulae (7a), (8a), (10a) and (11a),

where n stands for 2 or 3, and the radical Ron the nitrogen in formula (10a) and (11a) is not equal to H.

6. The compound according to claim 1 , selected from compounds of formulae (7c), (8c), (10c) and (11c),

where n stands for 2 or 3, and the radical R on the nitrogen in formula (10c) and (11c) is not equal to H.

7. The compound according to claim 1 , selected from compounds of formula (12),

8. The compound according to claim 1 , characterised in that L, for n=2, is selected from a single bond, CR 2 , O, NR or C(═O) or, for n=3, stands for N or, for n>2, is selected from an aromatic or heteroaromatic ring system having 5 to 24 aromatic ring atoms, which is optionally substituted by one or more radicals R.

9. The compound according to claim 1 , characterised in that at least one radical R is selected from the group consisting of an aromatic or heteroaromatic ring system having 5 to 24 aromatic ring atoms, which is optionally substituted by one or more radicals R 1 , and/or in that at least one radical R is selected from —C(═O)Ar 1 or —P(═O)(Ar 1 ) 2 and/or in that at least one radical R is selected from triaryl- or heteroarylamine derivatives and/or at least one substituent R stands for —N(Ar 1 ) 2 .

10. The compound according to claim 1 , characterised in that at least one group R is selected from the group consisting of benzene, biphenyl, terphenyl, quaterphenyl, fluorene, spirobifluorene, naphthalene, pyrrole, furan, thiophene, indole, benzofuran, benzothiophene, carbazole, dibenzothiophene, dibenzofuran, 1,3,5-triazine, pyridine, pyrimidine, pyrazine, pyridazine, indenocarbazole, bridged carbazole, indolocarbazole, anthracene, phenanthrene, pyrene, triphenylene, benzanthracene, quinoline, isoquinoline, phenanthridine, phenanthroline, azacarbazole, imidazole, pyrazole, thiazole, oxazole, oxadiazole, triazole, benzimidazole and combinations of two, three or four of these groups, where the groups are each optionally substituted by one or more radicals R 1 .

11. A formulation comprising at least one compound according to claim 1 and at least one further compound.

12. The formulation according to claim 11 , wherein the at least one further compound is an organic solvent.

13. A method comprising incorporating the compound according to claim 1 in an electronic device.

14. An electronic device comprising at least one compound according to claim 1 .

15. The electronic device according to claim 14 , wherein the electronic device is an organic electroluminescent device, characterised in that the at least one compound is employed as matrix material for a fluorescent or phosphorescent emitter and/or in a hole-blocking layer and/or in an electron-transport layer.

16. The electronic

Assignees

• Merck Patent Gmbh

Inventors

• Stoessel Philipp
• Parham Amir Hossain
• Pflumm Christof
• Jatsch Anja
• Eberle Thomas
• Kroeber Jonas Valentin

Classifications

• C09K11/02

  Use of particular materials as binders, particle coatings or suspension media therefor · CPC title

• C09K2211/1092

  containing sulfur as the only heteroatom · CPC title

• H01L2251/308

  Electricity · mapped topic

• H01L51/0058

  Electricity · mapped topic

• H01L51/5221

  Electricity · mapped topic