Compounds for electronic devices

1. A compound of a formula (1-A-1) or formula (1-A-2)

where the following applies to the symbols and indices occurring:

Ar* is on each occurrence, identically or differently, an aromatic ring system having 6 to 24 aromatic ring atoms selected from the formulae (A-1) to (A-20)

wherein R 2 in formulae (A-17) to (A-20), is identically or differently H, alkyl groups having 1 to 20 C atoms, or phenyl; or an electron-rich heteroaryl group having 5 to 18 aromatic ring atoms, each of which is optionally substituted by one or more radicals R 2′ ;

L is on each occurrence a single bond;

R 1 is on each occurrence, identically or differently, H, D, F, Cl, Br, I, C(═O)R 3 , CN, Si(R 3 ) 3 , NO 2 , P(═O)(R 3 ) 2 , S(═O)R 3 , S(═O) 2 R 3 , a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl or alkynyl group having 2 to 20 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 3 and where one or more CH 2 groups in the above-mentioned groups is optionally replaced by —R 3 C═CR 3 —, —C≡C—, Si(R 3 ) 2 , C═O, C═S, C═NR 3 , —C(═O)O—, —C(═O)NR 3 —, NR 3 , P(═O)(R 3 ), —O—, —S—, SO or SO 2 and where one or more H atoms in the above-mentioned groups is optionally replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic ring system having 6 to 30 aromatic ring atoms, which may in each case be substituted by one or more radicals R 3 , where two or more non-aromatic radicals R 1 is optionally linked to one another and may form a ring;

R 2′ is on each occurrence H;

R 3 is on each occurrence, identically or differently, H, D, F, Cl, Br, I, C(═O)R 4 , CN, Si(R 4 ) 3 , NO 2 , P(═O)(R 4 ) 2 , S(═O)R 4 , S(═O) 2 R 4 , a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl or alkynyl group having 2 to 20 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 4 and where one or more CH 2 groups in the above-mentioned groups is optionally replaced by —R 4 C═CR 4 —, —C≡C—, Si(R 4 ) 2 , C═O, C═S, C═NR 4 , —C(═O)O—, —C(═O)NR 4 —, NR 4 , P(═O)(R 4 ), —O—, —S—, SO or SO 2 and where one or more H atoms in the above-mentioned groups is optionally replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms, which may in each case be substituted by one or more radicals R 4 , or an aryloxy or heteroaryloxy group having 5 to 30 aromatic ring atoms, which is optionally substituted by one or more radicals R 4 , where two or more radicals R 3 is optionally linked to one another and optionally forms a ring;

R 4 is on each occurrence, identically or differently, H, D, F or an aliphatic, aromatic or heteroaromatic organic radical having 1 to 20 C atoms, in which, in addition, one or more H atoms is optionally replaced by D or F; two or more substituents R 4 here is optionally linked to one another and may form a ring;

where the compound does not contain a carbazole group; and

where at least one group Ar* which represents an electron-rich heteroaryl group having 5 to 18 aromatic ring atoms or an aromatic ring system having 12 to 24 aromatic ring atoms must be present in the compound.

2. The compound according to claim 1 , wherein

a) the group Ar* conforms to the following formula (H)

where

Y is NR 2 , PR 2 , O or S; and

p is on each occurrence equal to 0 or 1, where, for p=0, radicals R 2 are bonded at the relevant positions, and where, for Y═NR 2 , the two indices p cannot both be equal to 1;

the group is substituted by radicals R 2 at all free positions, and

the group R 2 is as defined in claim 1 , and

the group is optionally connected to the group L at any position, where the bonding may also occur at the site of the bond NR 2 or PR 2 ; or

b) the group Ar* is selected from the formulae (A-1) to (A-20)

wherein R 2 in formulae (A-17) to (A-20), is identically or differently H, alkyl groups having 1 to 20 C atoms, or phenyl.

3. The compound according to claim 2 , wherein

the group Ar* conforms to the following formula (H) and

Y is O or S;

p is 1; and

the group Ar* is connected to the group L at any position.

4. The compound according to claim 3 , wherein

R 1 is identically or differently, H, D, a straight-chain alkyl or alkoxy group having 1 to 10 C atoms or a branched or cyclic alkyl or alkoxy group having 3 to 10 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 3 , or an aromatic ring system having 6 to 12 aromatic ring atoms, which may in each case be substituted by one or more radicals R 3 , and

R 3 is on each occurrence, identically or differently, H, D, F, CN, Si(R 4 ) 3 or a straight-chain alkyl or alkoxy group having 1 to 10 C atoms or a branched or cyclic alkyl or alkoxy group having 3 to 10 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 4 , or 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 4 ,

R 4 is on each occurrence, identically or differently, H, D, F or an aliphatic, aromatic or heteroaromatic organic radical having 1 to 20 C atoms, in which, in addition, one or more H atoms may be replaced by D or F.

5. The compound according to claim 1 , wherein the bonding position of the group L-Ar* to the aromatic six-membered ring of the basic structure of the formula (1-A-1) or formula (1-A-2) is in the para- or meta-position to the nitrogen atom.

6. The compound according to claim 1 , wherein the groups R 1 of the group C(R 1 ) 2 , do not represent an aromatic ring system and do not represent an aryl group.

7. The compound according to claim 1 , wherein the compound contains no electron-deficient heteroaryl group and no keto group, no phosphorus oxide group and no sulfur oxide group.

8. A process for the preparation of the compound according to claim 1 , which comprises one or more transition metal-catalysed, coupling reactions by means of which aryl or heteroaryl groups are introduced as substituents are carried out starting from a dihydroacridine derivative.

9. An oligomer, polymer or dendrimer containing one or more compounds according to claim 1 , where the bond(s) to the polymer, oligomer or dendrimer is optionally localised at any position in formula (1-A-1) or formula (1-A-2) that are substituted by R 1 or R 2 .

10. A formulation comprising at least one polymer, oligomer or dendrimer according to claim 9 and at least one solvent.

11. An electronic device comprising at least one polymer, oligomer or dendrimer according to claim 9 .

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

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

14. The electronic device according to claim 13 , wherein the device is 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 optical detector, an organic photoreceptor, an organic field-quench device, a light-emitting electrochemical cell, an organic laser diode or an organic electroluminescent device.

15. An organic electroluminescent device which comprises the compound according to claim 1 is employed in one or more of the following functions:

as hole-transport material in a hole-transport or hole-injection layer,

as matrix material in an emitting layer,

as electron-blocking material or

as exciton-blocking material.

16. The compound according to claim 1 , wherein at least one group Ar* which represents an aromatic ring system having 12 to 24 aromatic ring atoms must be present in the compound.

17. The compound according to claim 16 , wherein

R 1 is identically or differently, H, D, a straight-chain alkyl or alkoxy group having 1 to 10 C atoms or a branched or cyclic alkyl or alkoxy group having 3 to 10 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 3 , or an aromatic ring system having 6 to 12 aromatic ring atoms, which may in each case be substituted by one or more radicals R 3 , and

R 3 is on each occurrence, identically or differently, H, D, F, CN, Si(R 4 ) 3 or a straight-chain alkyl or alkoxy group having 1 to 10 C atoms or a branched or cyclic alkyl or alkoxy group having 3 to 10 C atoms, where the above-mentioned groups may each be substituted by one or more radicals R 4 , or 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 4 ,

R 4 is on each occurrence, identically or differently, H, D, F or an aliphatic, aromatic or heteroaromatic organic radical having 1 to 20 C atoms, in which, in addition, one or more H atoms may be replaced by D or F.