Spiro dihydroacridine derivatives and the use thereof as materials for organic electroluminescence devices
The present invention relates to compounds of formulae (1), (2) or (3) that are suitable for use in electronic devices, and to electronic device, in particular organic electroluminescence devices, containing these compounds.
1. A compound of the formula (1), (2) or (3)
where the following applies to the symbols and indices used:
Y is O;
X is on each occurrence, identically or differently, CR 2
Ar is on each occurrence, identically or differently, an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which is optionally substituted by one or more radicals R 3 ; the group Ar and the adjacent group X, which in this case stands for C, may also be bridged to one another here by a single bond or a divalent group selected from C(R 3 ) 2 , NR 3 , O or S;
L is on each occurrence, identically or differently, a single bond or a divalent group;
R 2 , R 3 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 4 ) 2 , C(═O)Ar 1 , C(═O)R 4 , 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 is optionally substituted by one or more radicals R 4 , 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═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 heteroaromatic 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 , where two or more adjacent substituents R 1 or R 3 may optionally form a monocyclic or polycyclic, aliphatic ring system or R 2 may form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which is optionally substituted by one or more radicals R 4 ;
wherein at least one of the radicals R 2 is selected from aromatic ring systems having 6 to 24 aromatic ring atoms and said aromatic ring systems do not contain any heteroatoms;
R 4 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 5 ) 2 , C(═O)Ar 1 , C(═O)R 5 , 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 is optionally substituted by one or more radicals R 5 , where one or more non-adjacent CH 2 groups is optionally replaced by R 5 C═CR 5 , C≡C, Si(R 5 ) 2 , C═O, C═S, C═NR 5 , P(═O)(R 5 ), SO, SO 2 , NR 5 , O, S or CONR 5 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 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R 5 , an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 5 , or a combination of these systems, where two or more adjacent substituents R 4 may optionally form a monocyclic or polycyclic, aliphatic ring system, which is optionally substituted by one or more radicals R 5 ;
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 5 ; two radicals Ar 1 which are bonded to the same N atom or P atom may also be bridged to one another here by a single bond or a bridge selected from N(R 5 ), C(R 5 ) 2 , O or S;
R 5 is selected on each occurrence, identically or differently, 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 or CN, where two or more adjacent substituents R 3 may form a mono- or polycyclic, aliphatic ring system with one another;
m is on each occurrence, identically or differently, 0 or 1;
n is 0;
p is 0 or 1.
2. The compound according to claim 1 , wherein
R 2 , R 3 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 4 ) 2 , C(═O)Ar 1 , C(═O)R 4 , 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 is optionally substituted by one or more radicals R 4 , where one or more non-adjacent CH 2 groups is optionally replaced by R 4 C═CR 4 , C≡C, Si(R 4 ) 2 , C═O, C═S, 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 heteroaromatic 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 ;
R 4 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 5 ) 2 , C(═O)Ar 1 , C(═O)R 5 , 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 is optionally substituted by one or more radicals R 5 , where one or more non-adjacent CH 2 groups is optionally replaced by R 5 C═CR 5 , C≡C, Si(R 5 ) 2 , C═O, C═S, C═NR 5 , P(═O)(R 5 ), SO, SO 2 , NR 5 , O, S or CONR 5 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 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R 5 , an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 5 ;
R 5 is selected on each occurrence, identically or differently, 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 or CN.
3. The compound according to claim 1 , wherein L stands, identically or differently on each occurrence, for a straight-chain alkylene, alkylidene, alkyleneoxy or thioalkyleneoxy group having 1 to 10 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, which is optionally substituted by in each case one or more radicals R 4 , where one or more non-adjacent CH 2 groups is optionally replaced by —R 4 C═CR 4 —, —C≡C—, Si(R 4 ) 2 , C═O, C═NR 4 , P(═O)R 4 , S═O, SO 2 , —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 , or P(R 4 ), P(═O)(R 4 ), N(Ar 1 ); or L is a single bond.
4. The compound according to claim 1 , selected from the compounds of the formulae (6) to (12),
where the symbols and indices used have the meanings given in claim 1 .
5. The compound according to claim 1 , selected from the compounds of the formulae (6a) to (12a),
where the symbols and indices used have the meanings given in claim 1 .
6. The compound according to claim 5 , wherein Ar is selected from the group consisting of benzene, ortho-, meta- or para-biphenyl, ortho-, meta-, para- or branched terphenyl, ortho-, meta- para- or branched quaterphenyl, 1- or 2-naphthyl, pyrrole, furan, thiophene, indole, benzothiophene, benzofuran, carbazole, dibenzofuran, dibenzothiophene, pyridine, pyrimidine, pyrazine, pyridazine, triazine, anthracene, phenanthrene, pyrene, benzanthracene or combinations of two or three of these groups, each of which is optionally substituted by one or more radicals R 3 .
7. The compound according to claim 1 , wherein Ar is selected from the group consisting of aromatic or heteroaromatic ring systems having 5 to 24 aromatic ring atoms, which may in each case be substituted by one or more radicals R 3 .
8. The compound according to claim 1 , wherein Ar is selected from the group consisting of benzene, ortho-, meta- or para-biphenyl, ortho-, meta-, para- or branched terphenyl, ortho-, meta- para- or branched quaterphenyl, 1- or 2-naphthyl, pyrrole, furan, thiophene, indole, benzothiophene, benzofuran, carbazole, dibenzofuran, dibenzothiophene, pyridine, pyrimidine, pyrazine, pyridazine, triazine, anthracene, phenanthrene, pyrene, benzanthracene or combinations of two or three of these groups, each of which is optionally substituted by one or more radicals R 3 .
9. The compound according to claim 1 , wherein at least one substituent R 2 and/or R 3 or a monovalent group Ar is selected from structures of the formulae (13) to (16) for R 1 to R 3 or the formulae (13), (15) or (16) for Ar,
and/or at least one divalent or trivalent group Ar is selected from the groups of the formulae (17) to (19),
where R 3 , R 4 and m have the meaning given in claim 1 , * indicates the position of the bonding of the group of the formula (13) to (19) and furthermore:
A is on each occurrence, identically or differently, CR 4 or N, with the proviso that one group A, two groups A or three groups A stand for N;
Ar 2 is, identically or differently on each occurrence, a divalent aromatic or heteroaromatic ring system having 5 to 16 C atoms, which is optionally substituted by one or more radicals R 4 ;
and/or in that at least one of the radicals R 1 , R 2 , R 3 or Ar is selected from the groups of the formulae (20) to (26), and/or at least one of the radicals Ar is selected from groups of the formulae (27) to (34),
where the symbols and indices used have the meanings given in claim 1 and above;
and/or in that at least one of the radicals R 1 , R 2 , R 3 or Ar is selected from the groups of the formulae (35) to (49),
where the symbols used have the meanings given in claim 1 and furthermore:
E is selected from the group consisting of C(R 4 ) 2 , NR 4 , O or S;
G is selected from the group consisting of NR 4 , O or S;
where R 4 is to be replaced by R 3 if the groups of the formulae (13), (15), (16), (20) to (26) and (35) to (49) stand for Ar and in the cases of the formulae (17) to (19) and (27) to (34).
10. A process for the preparation of the compound according to claim 1 , comprising the reaction steps:
a) building-up the halogenated skeleton; and
b) introducing substituents via a transition-metal-catalysed coupling reaction.
11. An oligomer, polymer or dendrimer containing one or more compounds according to claim 1 , where one or more bonds are present from the compound to the polymer, oligomer or dendrimer.
12. An electronic device which comprises the compound according to claim 1 .
13. The electronic device as claimed in claim 12 , wherein the device is 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.
14. An organic electroluminescent device in which the compound according to claim 1 is employed as matrix material for fluorescent or phosphorescent emitters and/or as fluorescent emitter and/or in an electron-blocking or exciton-blocking layer and/or in a hole-transport layer and/or in a hole-blocking layer and/or in an electron-transport layer and/or in an optical coupling-out layer.
15. A compound of the formula (2) or (3)
where the following applies to the symbols and indices used:
Y is on each occurrence, identically or differently, O or S;
X is on each occurrence, identically or differently, CR 2 or N; or two adjacent X stand for S, O or NR 2 , so that a five-membered ring arises; or two adjacent X stand for a group of the following formula (4) or (5),
where ^ indicates the corresponding adjacent groups X in the formula (1), (2) or (3);
X here stands for C if a group Ar or L is bonded to this group X in formula (2) or (3);
V is on each occurrence, identically or differently, C(R 2 ) 2 , NR 2 , O or S;
Z is on each occurrence, identically or differently, CR 2 or N;
Ar is on each occurrence, identically or differently, an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which is optionally substituted by one or more radicals R 3 ; the group Ar and the adjacent group X, which in this case stands for C, may also be bridged to one another here by a single bond or a divalent group selected from C(R 3 ) 2 , NR 3 , O or S;
L is on each occurrence, identically or differently, a single bond or a divalent group;
R 2 , R 3 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 4 ) 2 , C(═O)Ar 1 , C(═O)R 4 , 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 is optionally substituted by one or more radicals R 4 , where one or more non-adjacent CH 2 groups is optionally replaced by R 4 C═CR 4 , C≡C, Si(R 4 ) 2 , C═O, C═S, 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 heteroaromatic 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 , where two or more adjacent substituents R 1 or R 3 may optionally form a monocyclic or polycyclic, aliphatic ring system or R 2 may form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which is optionally substituted by one or more radicals R 4 ;
wherein at least one of the radicals R 2 is selected from aromatic ring systems having 6 to 24 aromatic ring atoms and said aromatic ring systems do not contain any heteroatoms;
R 4 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 5 ) 2 , C(═O)Ar 1 , C(═O)R 5 , 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 is optionally substituted by one or more radicals R 5 , where one or more non-adjacent CH 2 groups is optionally replaced by R 5 C═CR 5 , Si(R 5 ) 2 , C═O, C═S, C═NR 5 , P(═O)(R 5 ), SO, SO 2 , NR 5 , O, S or CONR 5 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 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R 5 , an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 5 , or a combination of these systems, where two or more adjacent substituents R 4 may optionally form a monocyclic or polycyclic, aliphatic ring system, which is optionally substituted by one or more radicals R 5 ;
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 5 ; two radicals Ar 1 which are bonded to the same N atom or P atom may also be bridged to one another here by a single bond or a bridge selected from N(R 5 ), C(R 5 ) 2 , O or S;
R 5 is selected on each occurrence, identically or differently, 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 or CN, where two or more adjacent substituents R 3 may form a mono- or polycyclic, aliphatic ring system with one another;
m is on each occurrence, identically or differently, 0 or 1;
n is 0, 1, 2, 3, 4 or 5;
p is 0 or 1.
16. The compound according to claim 15 , wherein Y is O.
17. The compound according to claim 15 , wherein all groups Y are selected identically.
18. The compound according to claim 15 , wherein X, identically or differently on each occurrence, stands for CR 2 or N, where a maximum of one group X per ring stands for N; or two adjacent groups X stand for a group of the formula (4) or (5), where Z stands, identically or differently on each occurrence, for CR 2 and V stands, identically or differently on each occurrence, for NR 2 or C(R 2 ) 2 .