Materials for organic electroluminescent devices
The present invention relates to a compound of the formula (1), to the use of the compound in an electronic device, and to an electronic device comprising a compound of the formula (1). The present invention furthermore relates to a formulation comprising one or more compounds of the formula (1).
1 . Compound of the formula (1),
where the following applies to the symbols and indices used:
X stands on each occurrence, identically or differently, for CR X or N;
Y 1 stands for B(R 0 ), Si(R 0 ) 2 , C═O, C═NR N , C═C(R 0 ) 2 , O, S, S═O, SO 2 , N(R N ), P(R 0 ) or P(═O)R 0 ;
Y 2 , Y 3 and Y 4 stand on each occurrence, identically or differently for B(R 0 ), C(R 0 ) 2 , Si(R 0 ) 2 , C═O, C═NR N , C═C(R 0 ) 2 , O, S, S═O, SO 2 , N(R N ), P(R 0 ) or P(═O)R 0 ;
R X , R 0 , R N stand on each occurrence, identically or differently, for H, D, F, Cl, Br, I, CHO, CN, C(═O)Ar, P(═O)(Ar) 2 , S(═O)Ar, S(═O) 2 Ar, N(R) 2 , N(Ar) 2 , NO 2 , Si(R) 3 , B(OR) 2 , OSO 2 R, a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 40 C atoms or a branched or a cyclic alkyl, alkoxy or thioalkyl group having 3 to 40 C atoms, each of which may be substituted by one or more radicals R, where in each case one or more non-adjacent CH 2 groups may be replaced by RC═CR, C≡C, Si(R) 2 , Ge(R) 2 , Sn(R) 2 , C═O, C═S, C═Se, P(═O)(R), SO, SO 2 , O, S or CONR and where one or more H atoms may be 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 may in each case be substituted by one or more radicals R, an aralkyl or heteroaralkyl group which has 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R, or an aryloxy group having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R; where two adjacent radicals R X may form an aliphatic, aromatic or heteroaromatic ring system together, which may be substituted by one or more radicals R; and where two adjacent radicals R 0 may form an aliphatic, aromatic or heteroaromatic ring system together, which may be substituted by one or more radicals R;
R stands on each occurrence, identically or differently, for H, D, F, Cl, Br, I, CHO, CN, C(═O)Ar, P(═O)(Ar) 2 , S(═O)Ar, S(═O) 2 Ar, N(R′) 2 , N(Ar) 2 , NO 2 , Si(R′) 3 , B(OR′) 2 , OSO 2 R′, a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 40 C atoms or a branched or a cyclic alkyl, alkoxy or thioalkyl group having 3 to 40 C atoms, each of which may be substituted by one or more radicals R′, where in each case one or more non-adjacent CH 2 groups may be replaced by R′C═CR′, C≡C, Si(R′) 2 , Ge(R′) 2 , Sn(R′) 2 , C═O, C═S, C═Se, P(═O)(R′), SO, SO 2 , O, S or CONR and where one or more H atoms may be 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 may in each case be substituted by one or more radicals R′; where two adjacent substituents R may form an aliphatic or aromatic ring system together, which may be substituted by one or more radicals R′;
Ar is, on each occurrence, identically or differently, an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may in each case also be substituted by one or more radicals R′;
R′ stands on each occurrence, identically or differently, for H, D, F, Cl, Br, I, CN, 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, where in each case one or more non-adjacent CH 2 groups may be replaced by SO, SO 2 , O, S and where one or more H atoms may be replaced by D, F, Cl, Br or I, or an aromatic or heteroaromatic ring system having 5 to 24 aromatic ring atoms;
n, m, p are on each occurrence, identically or differently, 0 or 1, whereas when n, m or p is 0, then the corresponding group Y 2 , Y 3 or Y 4 is absent and the bonds to Y 2 , Y 3 and Y 4 are replaced by groups X, and wherein at least one of the index n, m or p is equal to 1.
2 . Compound according to claim 1 , characterized in that m+p is equal to 1 or 2.
3 . Compound according to claim 1 , characterized in that Y 1 stands for B(R 0 ), O, S or N(R N ).
4 . Compound according to claim 1 , characterized in that Y 1 stands for N(R N ).
5 . Compound according to claim 1 , characterized Y 2 , Y 3 and Y 4 stand on each occurrence, identically or differently for B(R 0 ), C(R 0 ) 2 , Si(R 0 ) 2 , C═O, O, S or N(R N ).
6 . Compound according to claim 1 , characterized at least one group Y 2 , Y 3 or Y 4 is present, which stands for N(R N ).
7 . Compound according to claim 1 , characterized in that it is selected from compounds of formulae (2) to (6),
8 . Compound according to claim 1 , characterized in that it is selected from compound (2-1) to (6-1),
9 . Compound according to claim 1 , characterized in that it is selected from compounds (2-1-1) to (6-1-2),
10 . Compound according to claim 1 , characterized in that it comprises at least one group R X , R N or R 0 , which is selected:
from branched or cyclic alkyl groups represented by the general following formula (RS-a)
wherein
R 22 , R 23 , R 24 are at each occurrence, identically or differently, selected from H, a straight-chain alkyl group having 1 to 10 carbon atoms, or a branched or cyclic alkyl group having 3 to 10 carbon atoms, where the above-mentioned groups may each be substituted by one or more radicals R 25 , and where two of radicals R 22 , R 23 , R 24 or all radicals R 22 , R 23 , R 24 may be joined to form a (poly)cyclic alkyl group, which may be substituted by one or more radicals R 25 ;
R 25 is at each occurrence, identically or differently, selected from a straight-chain alkyl group having 1 to 10 carbon atoms, or a branched or cyclic alkyl group having 3 to 10 carbon atoms;
with the proviso that at each occurrence at least one of radicals R 22 , R 23 and R 24 is other than H, with the proviso that at each occurrence all of radicals R 22 , R 23 and R 24 together have at least 4 carbon atoms and with the proviso that at each occurrence, if two of radicals R 22 , R 23 , R 24 are H, the remaining radical is not a straight-chain;
from branched or cyclic alkoxy groups represented by the general following formula (RS-b)
wherein
R 26 , R 27 , R 28 are at each occurrence, identically or differently, selected from H, a straight-chain alkyl group having 1 to 10 carbon atoms, or a branched or cyclic alkyl group having 3 to 10 carbon atoms, where the above-mentioned groups may each be substituted by one or more radicals R 25 as defined above, and where two of radicals R 26 , R 27 , R 28 or all radicals R 26 , R 27 , R 28 may be joined to form a (poly)cyclic alkyl group, which may be substituted by one or more radicals R 25 as defined above;
with the proviso that at each occurrence only one of radicals R 26 , R 27 and R 28 may be H;
from aralkyl groups represented by the general following formula (RS-c)
wherein
R 29 , R 30 , R 31 are at each occurrence, identically or differently, selected from H, a straight-chain alkyl group having 1 to 10 carbon atoms, or a branched or cyclic alkyl group having 3 to 10 carbon atoms, where the above-mentioned groups may each be substituted by one or more radicals R 32 , 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 32 , and where two or all of radicals R 29 , R 30 , R 31 may be joined to form a (poly)cyclic alkyl group or an aromatic ring system, each of which may be substituted by one or more radicals R 32 ;
R 32 is at each occurrence, identically or differently, selected from a straight-chain alkyl group having 1 to 10 carbon atoms, or a branched or cyclic alkyl group having 3 to 10 carbon atoms, or an aromatic ring system having 6 to 24 aromatic ring atoms;
with the proviso that at each occurrence at least one of radicals R 29 , R 30 and R 31 is other than H and that at each occurrence at least one of radicals R 29 , R 30 and R 31 is or contains an aromatic ring system having at least 6 aromatic ring atoms; or
from aromatic ring systems represented by the general following formula (RS-d)
wherein
R 40 to R 44 is at each occurrence, identically or differently, selected from H, a straight-chain alkyl group having 1 to 10 carbon atoms, or a branched or cyclic alkyl group having 3 to 10 carbon atoms, where the above-mentioned groups may each be substituted by one or more radicals R 32 , 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 32 , and where two or more of radicals R 40 to R 44 may be joined to form a (poly)cyclic alkyl group or an aromatic ring system, each of which may be substituted by one or more radicals R 32 as defined above;
where the dashed bonds indicate the bonding of the corresponding group R X , R N or R 0 to the rest of the structure.
11 . Compound according to claim 1 , characterized in that it comprises at least one group R X , R N or R 0 , which is selected from a group of formula (ArL-1),
where the dashed bond in formula (ArL-1) indicates the bonding of the corresponding group R X , R N or R 0 to the rest of the structure, where Ar 2 , Ar 3 stand on each occurrence, identically or differently, for 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; and where m is an integer selected from 1 to 10.
12 . Polymer, oligomer or dendrimer containing one or more compounds according to claim 1 , where the bond(s) to the polymer, oligomer or dendrimer may be localised at any positions in formula (1) which is substituted by R X , R 0 , R N or R.
13 . Formulation comprising at least one compound according to claim 1 or at least one polymer, oligomer or dendrimer and at least one solvent.
14 . Electronic device comprising at least one compound according to claim 1 or at least one polymer, oligomer or dendrimer, 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.
15 . Organic electroluminescent device comprising at least one compound according to claim 1 characterised in that the compound dendrimer is employed as an emitter in an emitting layer.
16 . Organic electroluminescent device according to claim 15 , characterized in that the compound is employed as a fluorescent emitter in an emitting layer, wherein the emitting layer comprises at least one further component selected from matrix materials.
17 . Organic electroluminescent device according to claim 15 , characterized in that the compound is employed as an emitter showing Thermally Activated Delayed Fluorescence in an emitting layer, wherein the emitting layer comprises at least one further component selected from matrix materials.
18 . Organic electroluminescent device according to claim 15 , characterized in that the compound is employed as a fluorescent emitter in an emitting layer, wherein the emitting layer comprises at least one sensitizer selected from phosphorescent compounds and thermally activated delayed fluorescence compounds.
19 . Organic electroluminescent device according to claim 18 , characterized in that the emitting layer further comprises at least one organic functional material selected from matrix materials.