Organic electroluminescent device

Patent metadata

Field	Value
Publication number	US-10249828-B2
Application number	US-201414782722-A
Country	US
Kind code	B2
Filing date	Mar 18, 2014
Priority date	Apr 8, 2013
Publication date	Apr 2, 2019
Grant date	Apr 2, 2019

Abstract

The present invention relates to organic electroluminescent devices which comprise mixtures of at least one matrix material of the formula (1) and an emitting material which has a small singlet-triplet separation.

First claim

The invention claimed is:

1. An organic electroluminescent device comprising cathode, anode and emitting layer, which consists of the following compounds:
(A) at least one luminescent organic compound which has a separation between the lowest triplet state T 1 and the first excited singlet state S 1 of ≤0.15 eV (TADF compound);
wherein the at least one TADF compound is a luminescent organic compound which is an aromatic compound which contains both donor and acceptor substituents, where the donor substituents are selected from the group consisting of diarylamino groups, heteroarylamino groups, carbazole groups and carbazole derivatives, which may in each case also be substituted, and where the acceptor substituents are selected from the group consisting of cyano groups and electron-deficient heteroaryl groups, which are optionally substituted, and which has a separation between the lowest triplet state T 1 and the first excited singlet state S 1 of <0.15 eV; and

(B) at least one compound of the formula (1),

where the following applies to the symbols used:
X is on each occurrence, identically or differently, CR or N, or a group X-X stands for a group of the following formula (2), with the proviso that at least one group X-X stands for a group of the formula (2) and that a maximum of one group X-X per ring stands for a group of the formula (2),

where the C atoms with the dashed bonds indicate the bonding of the group;

Y 1 , Y 2 are selected on each occurrence, identically or differently, from the group consisting of CR 2 , NR, O, S, SiR 2 , BR, PR and P(═O)R;
E is selected on each occurrence, identically or differently, from the group consisting of a single bond, CR 2 , NR, O, S, SiR 2 , BR, PR and P(═O)R;
W is on each occurrence, identically or differently, CR or N;
R is selected on each occurrence, identically or differently, from the group consisting of H, D, F, Cl, Br, I, CN, NO 2 , N(Ar) 2 , N(R 1 ) 2 , C(═O)Ar, C(═O)R 1 , 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 1 , where one or more non-adjacent CH 2 groups is optionally replaced by R 1 C═CR 1 , C≡C, Si(R 1 ) 2 , C═O, C═S, C═NR 1 , P(═O)(R 1 ), SO, SO 2 , NR 1 , O, S or CONR 1 and where one or more H atoms is optionally replaced by D, F, CI, Br, I, CN or NO 2 , an aromatic or heteroaromatic ring system having 5 to 80, which may in each case be substituted by one or more radicals R′, an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 1 , or an aralkyl or heteroaralkyl group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 1 , where two or more adjacent substituents R may optionally form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which is optionally substituted by one or more radicals R 1 ;
R 1 is selected on each occurrence, identically or differently, 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 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 2 , where one or more non-adjacent CH 2 groups is optionally replaced by R 2 C═CR 2 , C≡C, Si(R 2 ) 2 , C═O, C═S, C═NR 2 , P(═O)(R 2 ), SO, SO 2 , NR 2 , O, S or CONR 2 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 2 , an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which is optionally substituted by one or more radicals R 2 , or an aralkyl or heteroaralkyl group having 5 to 60 aromatic ring atoms, where two or more adjacent substituents R 1 may optionally form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which is optionally substituted by one or more radicals R 2 ;
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 2 ; two radicals Ar which are bonded to the same N atom or P atom here may also be bridged to one another by a single bond or a bridge selected from N(R 2 ), C(R 2 ) 2 , O or S; and
R 2 is selected 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 2 may form a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring system with one another.

2. The organic electroluminescent device according to claim 1 , wherein the TADF compound in a layer in a mixture with the compound of the formula (1) has a luminescence quantum efficiency of at least 40%.

3. The organic electroluminescent device according to claim 1 , wherein the separation between S 1 and T 1 of the TADF compound is ≤0.10 eV.

4. The organic electroluminescent device according to claim 1 , wherein the following applies to the LUMO of the TADF compound LUMO(TADF) and the HOMO of the compound of the formula (1) HOMO(matrix):
LUMO(TADF)−HOMO(matrix)>S 1 (TADF)−0.4eV,

where S 1 (TADF) is the first excited singlet state S 1 of the TADF compound.

5. The organic electroluminescent device according to claim 1 , wherein the lowest triplet energy of the compound of the formula (1) is a maximum of 0.1 eV lower than the triplet energy of the TADF compound.

6. The organic electroluminescent device according to claim 1 , wherein E is selected on each occurrence, identically or differently, from the group consisting of a single bond, CR 2 , NR, O and S.

7. The organic electroluminescent device according to claim 1 , wherein the compound of the formula (1) is selected from the compounds of the formulae (3) to (9),

wherein W, Y 1 , Y 2 , R, R l and R 2 have the meanings given in claim 1 and furthermore:
X is on each occurrence, identically or differently, CR or N.

8. The organic electroluminescent device according to claim 1 , wherein a maximum of one symbol X per ring stands for N and in that a maximum of one symbol W per ring stands for N.

9. The organic electroluminescent device according to claim 1 , wherein the compound of the formula (1) is selected from the compounds of the formulae (3a) to (9a),

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

10. The organic electroluminescent device according to

Assignees

• Merck Patent Gmbh

Inventors

• Stoessel Philipp
• Parham Amir Hossain
• Pflumm Christof
• Jatsch Anja
• Kaiser Joachim

Classifications

• C09K2211/1007

  Non-condensed systems · CPC title

• C09K2211/1033

  with oxygen · CPC title

• C09K2211/1029

  containing one nitrogen atom as the heteroatom · CPC title

• C09K2211/1014

  bridged by heteroatoms, e.g. N, P, Si or B · CPC title

• C09K2211/1059

  containing three nitrogen atoms as heteroatoms · CPC title