Materials for organic electroluminescent devices

1. A compound of the formula (1) or formula (2),

where the following applies to the symbols used:

pym is a pyrimidine, which is optionally substituted by one or more radicals R;

Cb is a carbazole derivative which contains at least 2 bridges, in which, in addition, one or more C atoms is optionally replaced by N and which is optionally substituted by one or more radicals R 2 ;

R, R 1 and R 2 are selected on each occurrence, identically or differently, and are H, D, F, Cl, Br, I, CN, NO 2 , N(Ar) 2 , N(R 3 ) 2 , C(═O)Ar, C(═O)R 3 , P(═O)(Ar) 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 is optionally substituted by one or more radicals R 3 , where one or more non-adjacent CH 2 groups is optionally replaced by R 3 C═CR 3 , C≡C Si(R 3 ) 2 , C═O, C═S, C═NR 3 , P(═O)(R 3 ), SO, SO 2 , NR 3 , O, S or CONR 3 and where one or more H atoms is optionally replaced by D, F, Cl, Br, I, CN or NO 2 , an aromatic or heteroaromatic ring system having 5 to 80 aromatic ring atoms, which may in each case be substituted by one or more radicals R 3 , an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 3 , or an aralkyl or heteroaralkyl group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 3 , where two or more adjacent substituents R 2 may optionally form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which is optionally substituted by one or more radicals R 3 ;

R 3 is on each occurrence, identically or differently, H, D, F, Cl, Br, I, CN, NO 2 , N(Ar) 2 , N(R 4 ) 2 , C(═O)Ar, C(═O)R 4 , P(═O)(Ar) 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 is optionally substituted by one or more radicals R 3 , where one or more non-adjacent CH 2 groups is optionally replaced by R 4 C═CR 4 , Si(R 4 ) 2 , C═O, C═S,C═Se, C═NR 4 , P(═O)(R 4 ), SO, SO 2 , NR 4 , O, S or CONR 4 and where one or more H atoms is optionally replaced by D, F, Cl, Br, I, CN or NO 2 , an aromatic or hetero-aromatic ring system having 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R 4 , an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 4 , or an aralkyl or heteroaralkyl group having 5 to 60 aromatic ring atoms, where two or more adjacent substituents R 3 may optionally form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which is optionally substituted by one or more radicals R 4 ;

Ar 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 4 ; two radicals Ar 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 4 ), C(R 4 ) 2 , O or S;

R 4 is 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 or CN, where two or more adjacent substituents R 4 may form a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring system with one another;

the following compounds are excluded from the invention:

2. The compound according to claim 1 , wherein the compounds of the formula (1) are selected from the compounds of the formulae (1 a), (1 b) or (1 c) and in that the compounds of the formula (2) are compounds of the formula (2a),

where the symbols used have the meanings given in claim 1 .

3. The compound according to claim 1 , wherein R 1 represents H or an aromatic or heteroaromatic ring system having 5 to 24 aromatic ring atoms, which is optionally substituted by one or more radicals R 3 .

4. The compound according to claim 1 , wherein the group pym is selected from the groups of the formulae (3), (4) or (5),

Where the symbols used have the meanings given in claim 1 and the dashed bond indicates the bond to the phenyl group in formula (1) or (2).

5. The compound according to claim 4 , wherein the group pym is selected from the formulae (3a), (4a) and (5a),

Where the symbols used have the meanings given in claim 1 and the dashed bond represents the bond from the pyrimidine to the phenyl group of the formula (1) or (2).

6. The compound according to claim 1 , wherein R stands, identically or differently on each occurrence, for H, an alkyl group having 1 to 10 C atoms or for an aromatic or heteroaromatic ring system having 5 to 24 aromatic ring atoms, which is optionally substituted by one or more radicals R 3 .

7. The compound according to claim 1 , wherein the group Cb is selected from the groups of the formulae (6) to (22),

where the symbols used have the meanings given in claim 1 , the dashed bond represents the bond from the carbazole derivative to the phenyl group of the formula (1) or (2) and

X is on each occurrence, identically or differently, CR 2 or N, where a maximum of 2 symbols X per ring stand for N;

Y is on each occurrence, identically or differently, C(R 2 ) 2 , NR 2 , O or S;

n is 0 or 1, where n equals 0 means that no group Y is bonded at this position and instead radicals R 2 are bonded to the corresponding carbon atoms.

8. The compound according to claim 7 , wherein the symbol X stands, identically or differently on each occurrence, for CR 2 .

9. The compound according to claim 7 , wherein the symbol X stands, identically or differently on each occurrence, CH.

10. The compound according to claim 1 , wherein the substituent R 2 , which is bonded directly to a nitrogen atom in the bridge of a carbazole derivative, stands for an aromatic or heteroaromatic ring system having 5 to 24 aromatic ring atoms, which may also be substituted by one or more radicals R 3 .

11. The compound according to claim 1 , wherein the group Cb is selected from the groups of the formulae (7), (8), (10), (11), (13), (14), (16) to (19), (21) and (22),

where the symbols used have the meanings given in claim 1 , the dashed bond represents the bond from the carbazole derivative to the phenyl group of the formula (1) or (2) and

X is on each occurrence, identically or differently, CR 2 or N, where a maximum of 2 symbols X per ring stand for N;

Y is on each occurrence, identically or differently, C(R 2 ) 2 , NR 2 , 0 or S;

n is 0 or 1, where n equals 0 means that no group Y is bonded at this position and instead radicals R 2 are bonded to the corresponding carbon atoms.

12. A mixture comprising at least one compound according to claim 11 and at least one further compound.

13. A mixture comprising at least one compound according to claim 11 and at least one further compound, wherein the one further compound is a fluores-cent or phosphorescent dopant.

14. A formulation comprising at least one compound or according to claim 11 and one or more solvents.

15. An electronic device which comprises the compound according to claim 11 .

16. An organic electroluminescent device which comprises the compound according to claim 11 .

17. The electronic device according to claim 15 , wherein the electronic device is an organic electroluminescent device, an organic integrated circuit, an organic field-effect transistor, an organic thin-film transistor, an organic light-emitting transistor, an organic solar cell, an organic dye-sensitised solar cell, an organic optical detector, an organic photoreceptor, an organic field-quench device, a light-emitting electrochemical cell, an organic laser diode or an organic plasmon emitting device.

18. An organic electroluminescent device which comprises the compound according to claim 11 is present as matrix material for fluorescent or phosphorescent emitters and/or in a hole-blocking layer and/or in an electron-transport layer.

19. A process for the preparation of the compound according to claim 1 , comprising the reaction steps:

a) synthesis of an optionally substituted phenylpyrimidine derivative which contains a reactive leaving groups on the phenyl group in the meta-position or in the ortho-position to the pyrimidine; and

b) coupling of this phenylpyrimidine derivative to a carbazole derivative.