Materials for organic electroluminescent devices

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

wherein

X is, identically or differently on each occurrence, N, P, or P═O;

Y1 is, identically or differently on each occurrence, C(R 1 ) 2 or NR 1 ;

Y 2 , Y 3 is, identically or differently on each occurrence, a single bond or C(R 1 ) 2 , NR 1 , O, S, C═O, C═NR 1 , C═C(R 1 ) 2 , Si(R 1 ) 2 , BR 1 , PR 1 , P(═O)R 1 , SO, or SO 2 ; with the proviso that if any one of Y 1 , Y 2 or Y 3 is NR 1 , then R 1 of NR 1 is an aromatic or heteroaromatic ring system, which is optionally substituted by one or more radicals R 2 ;

Ar 1 is, identically or differently on each occurrence, a group of the following formula (3), formula (4), or formula (5),

wherein the group is bonded to X and to Y 1 via the two positions denoted by * and wherein the group is optionally bonded to Y 3 via a further adjacent position and wherein

W is, identically or differently on each occurrence, C or N;

V for W═C, is, identically or differently on each occurrence, CR, N, NR, S, or O, with the proviso that precisely one symbol V stands for NR, S, or O; or, for W═N is, identically or differently on each occurrence, CR or N;

Q is on each occurrence, identically or differently; CR or N;

wherein V or Q stands for C if a group Y 3 is bonded to this group V or Q;

Ar 2 , Ar 3 is, identically or differently on each occurrence, an aryl or heteroaryl group having 5 to 18 aromatic ring atoms, optionally substituted by one or more radicals R;

L is a di-, tri-, tetra-, penta- or hexavalent straight-chain alkylene, alkylidene, alkyleneoxy, or thioalkyleneoxy group having 1 to 40 C atoms, or a branched or cyclic alkylene, alkylidene, alkyleneoxy, or thioalkyleneoxy group having 3 to 40 C atoms, or an alkenylene or alkynylene group having 2 to 40 C atoms, optionally substituted by in each case one or more radicals R 2 , wherein one or more non-adjacent CH 2 groups are optionally replaced by —R 2 C═CR 2 —, —C≡C—, Si(R 2 ) 2 , C═O, C═NR 2 , P(═O)R 2 , S═O, SO 2 , —O—, —S—, or —CONR 2 —, and wherein one or more H atoms are optionally replaced by D, F, Cl, Br, I, CN, or NO 2 , or a di-, tri-, tetra-, penta- or hexavalent aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, optionally substituted by one or more radicals R 2 , or P(R 2 ) 3-p , P(═O)(R 2 ) 3-p , C(R 2 ) 4-p , Si(R 2 ) 4-p , N(Ar) 3-p , or a combination of two, three, four, or five of these systems; or L is a chemical bond; L is bonded to any desired position of Ar 1 , Ar 2 , Ar 3 , Y 1 , Y 2 or Y 3 instead of a radical R or R 1 ;

R, R 1 is, identically or differently on each occurrence, selected from the group consisting of H, D, F, Cl, Br, I, CN, NO 2 , N(Ar) 2 , N(R 2 ) 2 , C(═O)Ar, C(═O)R 2 , P(═O)(Ar) 2 , a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 40 C atoms, a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 40 C atoms, and an alkenyl or alkynyl group having 2 to 40 C atoms, each of which is optionally substituted by one or more radicals R 2 , wherein one or more non-adjacent CH 2 groups are optionally replaced by R 2 C═CR 2 , C≡C, Si(R 2 ) 2 , Ge(R 2 ) 2 , Sn(R 2 ) 2 , C═O, C═S, C═Se, C═NR 2 , P(═O)(R 2 ), SO, SO 2 , NR 2 , O, S, or CONR 2 , and wherein one or more H atoms are optionally replaced by D, F, Cl, Br, I, CN, NO 2 , an aromatic or heteroaromatic ring system having 5 to 80, aromatic ring atoms, optionally substituted by one or more radicals R 2 , an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, optionally substituted by one or more radicals R 2 , or an aralkyl or heteroaralkyl group having 5 to 60 aromatic ring atoms, optionally substituted by one or more radicals R 2 , wherein two or more adjacent substituents R or two substituents R 1 which are bonded in the same group Y optionally define a mono- or polycyclic, aliphatic, aromatic, or heteroaromatic ring system, optionally substituted by one or more radicals R 2 ;

R 2 is, identically or differently on each occurrence, selected from the group consisting of 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, 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, optionally substituted by one or more radicals R 3 , wherein one or more non-adjacent CH 2 groups are optionally replaced by R 3 C═CR 3 , C≡C, Si(R 3 ) 2 , Ge(R 3 ) 2 , Sn(R 3 ) 2 , C═O, C═S, C═Se, C═NR 3 , P(O)(R 3 ), SO, SO 2 , NR 3 , O, S, or CONR 3 , and wherein one or more H atoms are optionally replaced by D, F, Cl, Br, I, CN, NO 2 , an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, optionally substituted by one or more radicals R 3 , an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, optionally substituted by one or more radicals R 3 , or an aralkyl or heteroaralkyl group having 5 to 60 aromatic ring atoms, wherein two or more adjacent substituents R 2 optionally define a monocyclic or polycyclic, aliphatic, aromatic, or heteroaromatic ring system, optionally substituted by one or more radicals R 3 ;

Ar is, identically or differently on each occurrence, an aromatic or heteroaromatic ring system having 5-30 aromatic ring atoms, optionally substituted by one or more non-aromatic radicals R 3 ; two radicals Ar which are bonded to the same N atom or P atom are optionally bridged to one another by a single bond or a bridge selected from N(R 3 ), C(R 3 ) 2 , O, or S;

R 3 is selected from the group consisting of H, D, F, CN, an aliphatic hydrocarbon radical having 1 to 20 C atoms, and an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms, in which one or more H atoms are optionally replaced by D, F, Cl, Br, I, or CN, wherein two or more adjacent substituents R 3 optionally define a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring system;

m, n are, identically or differently on each occurrence, 0 or 1, wherein m=0 or n=0 means that no group Y is present;

p is 2, 3, 4, 5, or 6, with the proviso that p is not greater than the maximum valence of L;

wherein the following compounds are excluded from the invention:

2. The compound of claim 1 , wherein Ar 2 and Ar 3 are, identically or differently on each occurrence, an aryl or heteroaryl group having 5 to 10 aromatic ring atoms, optionally substituted by one or more radicals R.

3. The compound of claim 1 , wherein the compound is selected from the compounds of formulae (5) to (11):

wherein

A is, identically or differently on each occurrence, CR or N; or two adjacent groups A together stand for NR, O or S, so that a five-membered ring arises; A is C if a group Y 2 or Y 3 is bonded to this A;

or selected from two or more compounds of the formulae (5) to (11), identical or different on each occurrence, connected to one another via L.

4. The compound of claim 1 , wherein the compound is selected from the compounds of formulae (5a) to (11a),

wherein

A is, identically or differently on each occurrence, CR or N; or two adjacent groups A together stand for NR, O or S, so that a five-membered ring arises; A is C if a group Y 2 or Y 3 is bonded to this A;

or selected from two or more compounds of the formulae (5a) to (11a), identical or different on each occurrence, connected to one another via L.

5. The compound of claim 1 , wherein the compound is selected from the compounds of formulae (5b) to (11b),

or selected from two or more compounds of the formulae (5b) to (11b), identical or different on each occurrence, connected to one another via L.

6. The compound of claim 1 , selected from the o the compounds of the formulae (5c) to (11c),

wherein

Ar 3a is a six-membered aryl ring group or a six-membered heteroaryl ring group, optionally substituted by one or more radicals R;

or selected from two or more compounds of the formulae (5c) to (11c), identical or different on each occurrence, connected to one another via L.

7. The compound of claim 1 , wherein X is nitrogen.

8. The compound of claim 1 , wherein Y 2 and Y 3 are, identically or differently on each occurrence, a single bond, C(R 1 ) 2 , or N(R 1 ).

9. The compound of claim 1 , wherein the compound is selected from the compounds of formulae (5d) to (11d),

or selected from two or more compounds of the formulae (5d) to (11d), identical or different on each occurrence, connected to one another via L.

10. The compound of claim 9 , wherein at least one radical R is selected from structures of the formulae (12) to (15),

and/or wherein at least one group L stands for a group selected from formulae (16) to (18),

wherein

* indicates the position of the bond of the group of the formula (12) to (18);

Z is, identically or differently on each occurrence, CR 2 or N, with the proviso that one group Z, two groups Z, or three groups Z, stand for N;

Ar 4 is, identically or differently on each occurrence, a divalent aryl or heteroaryl group having 5 to 18 C atoms, optionally substituted by one or more radicals R 2 ;

q is on each occurrence, identically or differently, 0, 1, 2, or 3;

and/or wherein at least one substituent R is selected from the group consisting of —NAr 2 , a triarylamine derivative, a carbazole derivative, an indenocarbazole derivative, an indolocarbazole derivative, an azacarbazole derivative, an indole derivative, a furan derivative, a benzofuran derivative, a dibenzofuran derivative, a thiophene derivative, a benzothiophene derivative, and a dibenzothiophene derivative, each of which is optionally substituted by one or more radicals R 2 .

11. The compound of claim 1 , wherein at least one radical R is selected from structures of the formulae (12) to (15),

and/or wherein at least one group L stands for a group selected from formulae (16) to (18),

wherein

* indicates the position of the bond of the group of the formula (12) to (18);

Z is, identically or differently on each occurrence, CR 2 or N, with the proviso that one group Z, two groups Z, or three groups Z, stand for N;

Ar 4 is, identically or differently on each occurrence, a divalent aryl or heteroaryl group having 5 to 18 C atoms, optionally substituted by one or more radicals R 2 ;

q is on each occurrence, identically or differently, 0, 1, 2, or 3;

and/or wherein at least one substituent R is selected from the group consisting of —NAr 2 , a triarylamine derivative, a carbazole derivative, an indenocarbazole derivative, an indolocarbazole derivative, an azacarbazole derivative, an indole derivative, a furan derivative, a benzofuran derivative, a dibenzofuran derivative, a thiophene derivative, a benzothiophene derivative, and a dibenzothiophene derivative, each of which is optionally substituted by one or more radicals R 2 .

12. A process for the preparation of the compound of claim 1 , said process comprising:

a) synthesizing a skeleton which carries a reactive leaving group instead of a group R; and

b) introducing the group R by a coupling reaction.

13. A formulation comprising at least one compound of claim 1 and one or more solvents.

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

15. An organic electroluminescent device comprising the compound of claim 1 as matrix material for fluorescent or phosphorescent emitters in an emitting layer and/or as hole-blocking material in a hole-blocking layer and/or as electron-transport material in an electron-transport layer and/or as electron-blocking or exciton-blocking material in an electron-blocking or exciton-blocking layer and/or as hole-transport material in a hole-transport layer or in a hole-injection layer.

16. The compound of claim 1 , wherein Ar 2 and Ar 3 are, identically or differently on each occurrence, selected from benzene, thiophene, pyrrole, furan, pyridine, pyrimidine, triazine, benzothiophene, indole, benzofuran, or naphthalene.

17. A mixture comprising at least one compound of claim 1 and at least one further compound.

18. A formulation comprising the mixture of claim 17 and one or more solvents.

19. An electronic device comprising the mixture of claim 17 .

20. An organic electroluminescent device comprising the mixture of claim 17 as matrix material for fluorescent or phosphorescent emitters in an emitting layer and/or as hole-blocking material in a hole-blocking layer and/or as electron-transport material in an electron-transport layer and/or as electron-blocking or exciton-blocking material in an electron-blocking or exciton-blocking layer and/or as hole-transport material in a hole-transport layer or in a hole-injection layer.