Composition for organic electronic device

文档序号：1471720 发布日期：2020-02-21 浏览：10次中文

阅读说明：本技术 用于有机电子器件的组合物 (Composition for organic electronic device ) 是由阿米尔·帕勒姆乔纳斯·克罗巴托比亚斯·格罗斯曼安雅·雅提斯奇克里斯蒂安·艾克霍夫于 2018-07-02 设计创作，主要内容包括：本发明涉及一种包含电子传输主体和空穴传输主体的组合物,其在电子器件中的用途以及包含所述组合物的电子器件。所述电子传输主体最优选地选自内酰胺类别。所述空穴传输主体优选地选自双咔唑类别。(The present invention relates to a composition comprising an electron transporting host and a hole transporting host, its use in an electronic device and an electronic device comprising said composition. The electron transport host is most preferably selected from the lactam class. The hole transporting host is preferably selected from the biscarbazole class.)

1. A composition comprising at least one compound of formula (1) and at least one compound of formula (2),

wherein the following applies to the symbols and labels used:

x, the same or different at each occurrence, is CR or N;

v is a bond, C (R)⁰)₂O or S;

v is 0 or 1;

X₂at each occurrence, identically or differently, CR¹Or N;

z is C (R)⁰)₂、NR¹O or S;

n is 0 or 1;

Ar₁and Ar₂In each case independently of one another, is an aromatic ring system having 6 to 40 aromatic ring atoms or a heteroaromatic ring system having 10 to 40 aromatic ring atoms, which may be interrupted by one or more radicals R³Substitution;

R⁰in each case identically or differently, straight-chain or branched alkyl having 1 to 4C atoms, or two R⁰Form a mono-or polycyclic aliphatic, aromatic or heteroaromatic ring system, which may be interrupted by one or more radicals R²Substitution;

r is selected, identically or differently on each occurrence, from H, D, F, Cl, Br, I, CN, NO₂，N(Ar)₂，N(R²)₂，C(＝O)Ar，C(＝O)R²，P(＝O)(Ar)₂，P(Ar)₂，B(Ar)₂，Si(Ar)₃，Si(R²)₃Straight-chain alkyl, alkoxy or thioalkyl having 1 to 20C atoms or branched or cyclic alkyl, alkoxy or thioalkyl having 3 to 20C atoms or alkenyl having 2 to 20C atoms, which radicals may in each case be substituted by one or more radicals R²Substitution of one or more non-adjacent CH₂The group can be represented by R²C＝CR²、Si(R²)₂、C＝O、C＝S、C＝NR²、P(＝O)(R²)、SO、SO₂、NR²O, S or CONR²And wherein one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂Instead, aromatic or heteroaromatic ring systems having from 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R²Substituted, or aryloxy or heteroaryloxy having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substituted or aralkyl or heteroaralkyl having 5 to 40 aromatic ring atoms, which aralkyl or heteroaralkyl may be substituted by one or more radicals R²Substitution; two substituents R bound to the same carbon atom or to adjacent carbon atoms may optionally form a mono-or polycyclic aliphatic, aromatic or heteroaromatic ringThe ring system may be substituted by one or more radicals R²Substitution;

R¹at each occurrence, identically or differently, selected from H, D, F, Cl, Br, I, CN, NO₂，N(Ar)₂，N(R²)₂，C(＝O)Ar，C(＝O)R²，P(＝O)(Ar)₂，P(Ar)₂，B(Ar)₂，Si(Ar)₃，Si(R²)₃Straight-chain alkyl, alkoxy or thioalkyl having 1 to 20C atoms or branched or cyclic alkyl, alkoxy or thioalkyl having 3 to 20C atoms or alkenyl having 2 to 20C atoms, which radicals may in each case be substituted by one or more radicals R²Substitution of one or more non-adjacent CH₂The group can be represented by R²C＝CR²、Si(R²)₂、C＝O、C＝S、C＝NR²、P(＝O)(R²)、SO、SO₂、NR²O, S or CONR²And wherein one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂Instead, aromatic or heteroaromatic ring systems having from 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R²Substituted, or aryloxy or heteroaryloxy having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substituted or aralkyl or heteroaralkyl having 5 to 40 aromatic ring atoms, which aralkyl or heteroaralkyl may be substituted by one or more radicals R²Substitution;

R²at each occurrence, identically or differently, selected from H, D, F, Cl, Br, I, CN, NO₂，N(Ar)₂，NH₂，N(R³)₂，C(＝O)Ar，C(＝O)H，C(＝O)R³，P(＝O)(Ar)₂Straight-chain alkyl, alkoxy or thioalkyl having 1 to 40C atoms or branched or cyclic alkyl, alkoxy or thioalkyl having 3 to 40C atoms or alkenyl or alkynyl having 2 to 40C atoms, which radicals may in each case be substituted by one or more radicals R³Substitution of one or more of them withAdjacent CH₂The radicals may be substituted by HC ═ CH, R³C＝CR³、C≡C、Si(R³)₂、Ge(R³)₂、Sn(R³)₂、C＝O、C＝S、C＝Se、C＝NR³、P(＝O)(R³)、SO、SO₂、NH、NR³O, S, CONH or CONR³And wherein one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂Instead, aromatic or heteroaromatic ring systems having from 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R³Substituted, or aryloxy or heteroaryloxy having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R³Substituted, or combinations of these systems, wherein two or more adjacent substituents R²May optionally form a mono-or polycyclic aliphatic, aromatic or heteroaromatic ring system which may be interrupted by one or more radicals R³Substitution;

R³selected, identically or differently on each occurrence, from H, D, F, CN, aliphatic hydrocarbon radicals having 1 to 20C atoms or aromatic ring systems having 6 to 30 ring atoms or heteroaromatic ring systems having 10 to 30 ring atoms, where one or more H atoms may be replaced by D, F, Cl, Br, I or CN and the ring systems may be substituted by one or more alkyl radicals each having 1 to 4 carbon atoms; two or more adjacent substituents R³Aliphatic ring systems which may form a single ring or multiple rings with one another;

ar is, identically or differently on each occurrence, an aromatic or heteroaromatic ring system having from 5 to 30 aromatic ring atoms, which may be substituted by one or more nonaromatic radicals R³Substitution; the two groups Ar bound to the same N, P or B atom may also be bound by a single bond or be chosen from N (R)³)、C(R³)₂The bridging groups of O or S are bridged to each other.

2. Composition according to claim 1, characterized in that the compound of formula (1) corresponds to formula (1a),

wherein the symbols and signs used have the same meaning as in claim 1.

3. Composition according to claim 1 or 2, characterized in that the compound of formula (2) corresponds to formula (2a),

where the symbols and indices used have the same meaning as in claim 1, q and t in each case independently of one another denote 0, 1,2,3 or 4, and r and s in each case independently of one another denote 0, 1,2 or 3.

4. Composition according to one or more of claims 1 to 3, characterized in that the substituent Ar is₁And Ar₂One of them represents an aromatic ring system having 6 to 40 aromatic ring atoms or a heteroaromatic ring system having 10 to 40 aromatic ring atoms, which may be interrupted by one or more radicals R³Substituted and the other substituent represents an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³And (4) substitution.

5. Composition according to one or more of claims 1 to 4, characterized in that the substituent Ar is₁And Ar₂In each case independently of one another denotes an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³And (4) substitution.

6. Composition according to one or more of claims 1 to 5, characterized in that it comprises at least one further compound chosen from: hole injection materials, hole transport materials, hole blocking materials, wide band gap materials, fluorescent emitters, phosphorescent emitters, host materials, electron blocking materials, electron transport materials, and electron injection materials, n-type dopants, and p-type dopants.

7. A formulation comprising a composition according to one or more of claims 1 to 6 and at least one solvent.

8. Use of a composition according to one or more of claims 1 to 6 in an organic electronic device.

9. Use according to claim 8, characterized in that the organic electronic device is selected from Organic Integrated Circuits (OIC), Organic Field Effect Transistors (OFET), Organic Thin Film Transistors (OTFT), organic electroluminescent devices, Organic Solar Cells (OSC), organic optical detectors and organic photoreceptors.

10. An organic electronic device comprising at least one composition according to one or more of claims 1 to 6.

11. The device according to claim 10, wherein the device is selected from the group consisting of Organic Integrated Circuits (OIC), Organic Field Effect Transistors (OFET), Organic Thin Film Transistors (OTFT), organic electroluminescent devices, Organic Solar Cells (OSC), organic optical detectors, and organic photoreceptors.

12. Device according to claim 10 or 11, characterized in that the device is an electroluminescent device selected from the group consisting of Organic Light Emitting Transistors (OLET), Organic Field Quenching Devices (OFQDs), organic light emitting electrochemical cells (OLEC, LEC, LEEC), organic laser diodes (O-laser) and Organic Light Emitting Diodes (OLED).

13. Device according to one or more of claims 10 to 12, characterized in that it comprises a composition according to one or more of claims 1 to 7 in the emitting layer (EML), in the Electron Transport Layer (ETL), in the Electron Injection Layer (EIL) and/or in the Hole Blocking Layer (HBL).

14. Device according to one or more of claims 10 to 13, characterized in that it comprises a composition according to one or more of claims 1 to 7 and a phosphorescent emitter in the light-emitting layer.

15. Method for manufacturing a device according to one or more of claims 10 to 14, characterized in that at least one organic layer comprising a composition according to one or more of claims 1 to 6 is applied by vapor deposition or from a solution.

16. Method according to claim 15, characterized in that at least one compound of formula (1) and at least one compound of formula (2) according to one of claims 1 to 6 are deposited from the gas phase, optionally together with other materials, from at least two material sources sequentially or simultaneously and form the organic layer.

17. The method according to claim 15, characterized in that a composition according to one or more of claims 1 to 6 is used as a material source for vapor deposition and the organic layer is formed.

18. The method according to claim 15, characterized in that the formulation according to claim 7 is used for applying the organic layer.

Technical Field

The present invention relates to a composition comprising an electron transporting host and a hole transporting host, its use in an electronic device and an electronic device comprising said composition. The electron transport host is particularly preferably selected from the lactam class. The hole transporting host is preferably selected from the biscarbazole class.

Background

The structure of organic electroluminescent devices (e.g. OLED-organic light emitting diodes or OLEC-organic light emitting electrochemical cells) in which organic semiconductors are employed as functional materials is described, for example, in US 4539507, US 5151629, EP 0676461 and WO 98/27136. In addition to fluorescent emitters, the light-emitting materials used here are increasingly organometallic complexes which exhibit phosphorescence instead of fluorescence (m.a. baldo et al, appl.phys.lett.1999, 75, 4-6). For quantum mechanical reasons, energy and power efficiency can be increased up to four times using organometallic compounds as phosphorescent emitters. However, in general, in the case of OLEDs, in particular in the case of OLEDs which exhibit triplet emission (phosphorescence), improvements are still required, for example in terms of efficiency, operating voltage and lifetime.

The properties of the organic electroluminescent device depend not only on the luminophor employed. Of particular importance here are also the other materials used, such as host and matrix materials, hole-blocking materials, electron-transporting materials, hole-transporting materials and electron-or exciton-blocking materials, in particular host or matrix materials thereof. Improvements in these materials can lead to significant improvements in electroluminescent devices.

Host materials for use in organic electronic devices are well known to those skilled in the art. The term matrix material is often also used in the prior art to denote the host material of the phosphorescent emitter. This use of the term is also applicable to the present invention. Meanwhile, various host materials for fluorescent and phosphorous optoelectronic devices have been developed.

According to the prior art, ketones (for example according to WO 2004/093207 or WO 2010/006680) or phosphine oxides (for example according to WO 2005/003253) are used in particular as matrix materials for phosphorescent emitters. Other matrix materials according to the prior art are triazines (e.g. WO2008/056746, EP 0906947, EP 0908787, EP 0906948) and lactams (e.g. WO 2011/137951). Furthermore, carbazole derivatives (for example according to WO 2005/039246, US2005/0069729 or WO 2014/015931), indolocarbazole derivatives (for example according to WO 2007/063754 or WO2008/056746) or indenocarbazole derivatives (for example according to WO 2010/136109 or WO 2011/000455), in particular those substituted by electron-deficient heteroaromatic groups (for example triazines), are used in particular according to the prior art as matrix materials for phosphorescent emitters. WO 2011/057706 discloses carbazole derivatives substituted by two triphenyltriazine groups. WO 2011/046182 discloses carbazole-arylidene-triazine derivatives substituted on triazines with fluorenyl groups. WO 2009/069442 discloses tricyclic compounds as host materials, such as carbazoles, dibenzofurans or dibenzothiophenes, which are highly substituted by electron-deficient heteroaromatic groups, such as pyridine, pyrimidine or triazine. WO 2011/057706 and WO 2015/169412 disclose other host materials including, inter alia, triazine-dibenzofuran-carbazole derivatives and triazine-dibenzothiophene-carbazole derivatives.

Another possibility for improving the performance data of electronic devices, in particular organic electroluminescent devices, is the use of a combination of two or more materials, in particular host materials or host materials.

US 6,392,250B 1 discloses the use of a mixture consisting of an electron transporting material, a hole transporting material and a fluorescent emitter in the light-emitting layer of an OLED. By means of such a mixture, the lifetime of the OLED can be improved compared to the prior art.

US 6,803,720B 1 discloses the use of a mixture comprising a phosphorescent emitter and a hole transporting material and an electron transporting material in the light emitting layer of an OLED. Both hole transport materials and electron transport materials are small organic molecules.

According to WO2011/137951, lactams can be used, for example, in admixture with triazine derivatives.

According to WO2013/064206, lactams can be used in admixture with, for example, biscarbazoles of the formula:

according to WO 2014/094964, lactams can be used in combination with biscarbazoles of the formula:

however, there is still a need for improvement in the use of these materials or in the use of mixtures of materials, in particular in terms of the lifetime of organic electronic devices.

It is therefore an object of the present invention to provide a material which is suitable for use in organic electronic devices, in particular organic electroluminescent devices, in particular fluorescent or phosphorescent OLEDs, and which leads to good device properties, in particular with regard to improved lifetime, and to provide corresponding electronic devices.

It has now been found that compositions comprising a compound of formula (1) and a hole transporting host of formula (2), preferably biscarbazole, achieve this object and overcome the disadvantages of the prior art, in particular the disadvantages of the prior art WO2013/064206 and WO 2014/094964. Compositions of this type lead to very good properties of organic electronic devices, in particular organic electroluminescent devices, in particular with respect to lifetime, and in particular also in the case of concentrations of the light-emitting components present in the light-emitting layer of from 2 to 15% by weight.

Disclosure of Invention

The invention therefore relates firstly to a composition comprising at least one compound of the formula (1) and at least one compound of the formula (2),

wherein the following applies to the symbols and labels used:

x, the same or different at each occurrence, is CR or N;

v is a bond, C (R)⁰)₂O or S;

v is 0 or 1;

X₂at each occurrence, identically or differently, CR¹Or N;

z is C (R)⁰)₂、NR¹O or S;

n is 0 or 1;

Ar₁and Ar₂In each case independently of one another, is an aromatic ring system having 6 to 40 aromatic ring atoms or a heteroaromatic ring system having 10 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³Substitution;

R⁰in each case identically or differently, a straight-chain or branched alkyl radical having 1 to 4C atoms or two R⁰Form a mono-or polycyclic aliphatic, aromatic or heteroaromatic ring system, which may be substituted by one or more radicals R²Substitution;

r is selected, identically or differently on each occurrence, from H, D, F, Cl, Br, I, CN, NO₂，N(Ar)₂，N(R²)₂，C(＝O)Ar，C(＝O)R²，P(＝O)(Ar)₂，P(Ar)₂，B(Ar)₂，Si(Ar)₃，Si(R²)₃Straight-chain alkyl, alkoxy or thioalkyl having 1 to 20C atoms or branched or cyclic alkyl, alkoxy or thioalkyl having 3 to 20C atoms or alkenyl having 2 to 20C atoms, which may in each case be substituted by one or more radicals R²Substitution of one or more non-adjacent CH₂The group can be represented by R²C＝CR²、Si(R²)₂、C＝O、C＝S、C＝NR²、P(＝O)(R²)、SO、SO₂、NR²O, S or CONR²And wherein one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂Instead, aromatic or heteroaromatic having 5 to 40 aromatic ring atomsA ring system which may be substituted in each case by one or more radicals R²Substituted, or aryloxy or heteroaryloxy having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substituted, or aralkyl or heteroaralkyl having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substitution; two substituents R which are bonded to the same carbon atom or to adjacent carbon atoms may optionally form a mono-or polycyclic aliphatic, aromatic or heteroaromatic ring system which may be interrupted by one or more radicals R²Substitution;

R¹at each occurrence, identically or differently, selected from H, D, F, Cl, Br, I, CN, NO₂，N(Ar)₂，N(R²)₂，C(＝O)Ar，C(＝O)R²，P(＝O)(Ar)₂，P(Ar)₂，B(Ar)₂，Si(Ar)₃，Si(R²)₃Straight-chain alkyl, alkoxy or thioalkyl having 1 to 20C atoms or branched or cyclic alkyl, alkoxy or thioalkyl having 3 to 20C atoms or alkenyl having 2 to 20C atoms, which may in each case be substituted by one or more radicals R²Substitution of one or more non-adjacent CH₂The group can be represented by R²C＝CR²、Si(R²)₂、C＝O、C＝S、C＝NR²、P(＝O)(R²)、SO、SO₂、NR²O, S or CONR²And wherein one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂Instead, aromatic or heteroaromatic ring systems having from 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R²Substituted, or aryloxy or heteroaryloxy having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substituted, or aralkyl or heteroaralkyl having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substitution;

R²at each occurrence, identically or differently, selected from H, D, F, Cl, Br, I, CN, NO₂，N(Ar)₂，NH₂，N(R³)₂，C(＝O)Ar，C(＝O)H，C(＝O)R³，P(＝O)(Ar)₂Straight-chain alkyl, alkoxy or thioalkyl having 1 to 40C atoms or branched or cyclic alkyl, alkoxy or thioalkyl having 3 to 40C atoms or alkenyl or alkynyl having 2 to 40C atoms, which may in each case be substituted by one or more radicals R³Substitution of one or more non-adjacent CH₂The radicals may be substituted by HC ═ CH, R³C＝CR³、C≡C、Si(R³)₂、Ge(R³)₂、Sn(R³)₂、C＝O、C＝S、C＝Se、C＝NR³、P(＝O)(R³)、SO、SO₂、NH、NR³O, S, CONH or CONR³And wherein one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂Instead, aromatic or heteroaromatic ring systems having from 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R³Substituted, or aryloxy or heteroaryloxy having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R³Substituted, or combinations of these systems, wherein two or more adjacent substituents R²May optionally form a mono-or polycyclic aliphatic, aromatic or heteroaromatic ring system, which may be substituted by one or more radicals R³Substitution;

R³selected, identically or differently on each occurrence, from H, D, F, CN, aliphatic hydrocarbon radicals having 1 to 20C atoms or aromatic ring systems having 6 to 30 ring atoms or heteroaromatic ring systems having 10 to 30 ring atoms, where one or more H atoms may be replaced by D, F, Cl, Br, I or CN and which may be substituted by one or more alkyl radicals each having 1 to 4 carbon atoms; two or more adjacent substituents R³Aliphatic ring systems which may form a single ring or multiple rings with one another;

The invention also relates to formulations comprising compositions of this type, to the use of these compositions in organic electronic devices, to organic electronic devices, preferably electroluminescent devices, comprising a composition of this type and preferably comprising the composition in one layer, and to a method of manufacturing a device of this type. The invention likewise relates to the corresponding preferred embodiments described below. By a specific selection of the known materials, in particular with regard to the selection of the hole transport material of formula (2), surprising and advantageous effects can be achieved.

As described above or preferably below, the layer comprising the composition comprising at least one compound of formula (1) and at least one compound of formula (2) is in particular an emitting layer (EML), an Electron Transport Layer (ETL), an Electron Injection Layer (EIL) and/or a Hole Blocking Layer (HBL).

In the case of the light-emitting layer, this is preferably a phosphorescent layer, characterized in that it comprises a phosphorescent emitter in addition to the compositions comprising the matrix materials of the formulae (1) and (2) as described above.

For the purposes of the present invention, adjacent carbon atoms are carbon atoms which are directly linked to one another.

For the purposes of the present description, the expression that two or more groups may form a ring with one another means in particular that the two groups are linked to one another by a chemical bond, with formal elimination of the two hydrogen atoms. This is illustrated by the following scheme:

however, in addition, the above expression also means that in the case where one of the two groups represents hydrogen, the second group is bonded at the position where the hydrogen atom is bonded, thereby forming a ring. This is illustrated by the following scheme:

for the purposes of the present invention, aryl contains 6 to 40 aromatic ring atoms, preferably C atoms. For the purposes of the present invention, heteroaryl groups contain 5 to 40 aromatic ring atoms, wherein the ring atoms contain a C atom and at least one heteroatom, with the proviso that the total number of C atoms and heteroatoms is at least 5. The heteroatoms are preferably selected from N, O and/or S. Aryl or heteroaryl is here a simple aromatic ring derived from benzene, i.e. phenyl, or a simple heteroaromatic ring, for example derived from pyridine, pyrimidine or thiophene, or a fused aryl or heteroaryl group, for example naphthalene, anthracene, phenanthrene, quinoline or isoquinoline.

For the purposes of the present invention, the aromatic ring system contains 6 to 40C atoms in the ring system and may be substituted by one or more radicals R³Is substituted in which R³Has the following meanings. The aromatic ring system also contains an aryl group as described above.

For the purposes of the present invention, heteroaromatic ring systems comprise 5 to 40 ring atoms and at least one heteroatom and may be substituted by one or more radicals R³Is substituted in which R³Has the following meanings. Preferred heteroaromatic ring systems have 10 to 40 ring atoms and at least one heteroatom and may be substituted by one or more radicals R³Is substituted in which R³Has the following meanings. The heteroaromatic ring system also comprises a heteroaryl group as described above. The heteroatoms in the heteroaromatic ring system are preferably selected from N, O and/or S.

For the purposes of the present invention, aromatic or heteroaromatic ring systems are understood to be those which do not necessarily comprise only aryl or heteroaryl groups, but in which a further plurality of aryl or heteroaryl groups may be interrupted by non-aromatic units (preferably less than 10% of non-H atoms), for example C, N or O atoms or carbonyl groups. Thus, for example, systems such as 9,9' -spirobifluorene, 9-diarylfluorene, triarylamine, diaryl ether, stilbene and the like should be considered as aromatic or heteroaromatic ring systems in the sense of the present invention, as well as systems in which two or more aryl groups are interrupted by, for example, linear or cyclic alkyl groups or silyl groups. Furthermore, the definition of aromatic or heteroaromatic ring system likewise covers systems in which two or more aryl or heteroaryl groups are bonded directly to one another, for example biphenyl, terphenyl, quaterphenyl or bipyridine.

In each case also by the radicals R³Aromatic or heteroaromatic ring systems having 5 to 40 aromatic ring atoms which are substituted and can be attached to the aromatic or heteroaromatic ring system via any desired position refer, for example, to groups derived from: benzene, naphthalene, anthracene, benzanthracene, phenanthrene, triphenylene, pyrene, chicory, perylene, fluoranthene, benzofluoranthene, tetracene, pentacene, benzopyrene, biphenyl, dibenzylidene, terphenyl, bistyryl, fluorene, spirobifluorene, dihydrophenanthrene, dihydropyrene, tetrahydropyrene, cis-or trans-indenofluorene, cis-or trans-monobenzindenofluorene, cis-or trans-dibenzindenofluorene, truxene, isotridecylindene, spirotricondene, spiroisotridecylindene, furan, benzofuran, isobenzofuran, dibenzofuran, thiophene, benzothiophene, isobenzothiophene, dibenzothiophene, pyrrole, indole, isoindole, carbazole, indolocarbazole, indenocarbazole, pyridine, quinoline, isoquinoline, acridine, phenanthridine, benzo-5, 6-quinoline, benzo-6, 7-quinoline, benzo-7, 8-quinoline, phenothiazine, benzene.

Oxazines, pyrazoles, indazoles, imidazoles, benzimidazoles, naphthoimidazoles, phenanthroimidazoles, pyridoimidazoles, pyrazinoimidazoles, quinoxaloimidazoles,

Azole, benzo

Azoles, naphtho

Azoles, anthracenes

Azole, phenanthro

Oxazole, iso

Oxazole, 1, 2-thiazole, 1, 3-thiazole, benzothiazole, pyridOxazines, benzopyridazines, pyrimidines, benzopyrimidines, quinoxalines, 1, 5-diaza-anthracenes, 2, 7-diaza-pyrenes, 2, 3-diaza-pyrenes, 1, 6-diaza-pyrenes, 1, 8-diaza-pyrenes, 4,5,9, 10-tetraazaperylene, pyrazines, phenazines, thiophenes

Oxazines, phenothiazines, fluoranthenes, naphthyridines, azacarbazoles, benzocarbazoles, phenanthrolines, 1,2, 3-triazoles, 1,2, 4-triazoles, benzotriazoles, 1,2,3-

Oxadiazole, 1,2,4-

Oxadiazole, 1,2,5-

Oxadiazole, 1,3,4-

Oxadiazoles, 1,2, 3-thiadiazoles, 1,2, 4-thiadiazoles, 1,2, 5-thiadiazoles, 1,3, 4-thiadiazoles, 1,3, 5-triazines, 1,2, 4-triazines, 1,2, 3-triazines, tetrazoles, 1,2,4, 5-tetrazines, 1,2,3, 4-tetrazines, 1,2,3, 5-tetrazines, purines, pteridines, indolizines and benzothiadiazoles.

The abbreviation Ar is, identically or differently on each occurrence, an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms, which may be substituted by one or more nonaromatic radicals R³Substitution; two groups Ar bound to the same N, P or B atom may also be bound by a single bond or be selected from N (R)³)、C(R³)₂The bridging groups of O or S are bridged to each other. Substituent R³Has been described above or preferably below.

For the purposes of the present invention, cyclic alkyl, alkoxy or thioalkoxy are understood to mean monocyclic, bicyclic or polycyclic radicals.

For the purposes of the present invention, in addition to individual H atoms or CH₂C whose groups may be substituted by the above-mentioned groups₁To C₂₀Alkyl isRefers to, for example, the following groups: methyl, ethyl, n-propyl, isopropyl, cyclopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, cyclobutyl, 2-methylbutyl, n-pentyl, sec-pentyl, tert-pentyl, 2-pentyl, neopentyl, cyclopentyl, n-hexyl, sec-hexyl, tert-hexyl, 2-hexyl, 3-hexyl, neohexyl, cyclohexyl, 1-methylcyclopentyl, 2-methylpentyl, n-heptyl, 2-heptyl, 3-heptyl, 4-heptyl, cycloheptyl, 1-methylcyclohexyl, n-octyl, 2-ethylhexyl, cyclooctyl, 1-bicyclo [ 2.2.2.2 ] n-bicyclo]Octyl, 2-bicyclo [2.2.2]Octyl, 2- (2, 6-dimethyl) octyl, 3- (3, 7-dimethyl) octyl, adamantyl, trifluoromethyl, pentafluoroethyl, 2,2, 2-trifluoroethyl, 1-dimethyl-n-hexyl-1-yl, 1-dimethyl-n-hept-1-yl, 1-dimethyl-n-oct-1-yl, 1-dimethyl-n-decan-1-yl, 1-dimethyl-n-dodecane-yl, 1-dimethyl-n-tetradec-1-yl, 1-dimethyl-n-hexadecan-1-yl, 1-dimethyl-n-octadecan-1-yl, 1, 1-diethyl-n-hexyl-1-yl, 1-diethyl-n-hept-1-yl, 1-diethyl-n-oct-1-yl, 1-diethyl-n-decan-1-yl, 1-diethyl-n-dodec-1-yl, 1-diethyl-n-tetradec-1-yl, 1-diethyl-n-hexadecan-1-yl, 1-diethyl-n-octadecan-1-yl, 1- (n-propyl) cyclohex-1-yl, 1- (n-butyl) cyclohex-1-yl, 1- (n-hexyl) cyclohex-1-yl, 1- (n-octyl) cyclohex-1-yl and 1- (n-decyl) cyclohex-1-yl .

Alkenyl means, for example, ethenyl, propenyl, butenyl, pentenyl, cyclopentenyl, hexenyl, cyclohexenyl, heptenyl, cycloheptenyl, octenyl, cyclooctenyl or cyclooctadienyl.

Alkynyl means, for example, ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl or octynyl.

C₁To C₂₀Alkoxy means, for example, methoxy, trifluoromethoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy, tert-butoxy or 2-methylbutoxy.

C₁To C₂₀Thioalkyl means, for example, S-alkyl, such as thiomethyl, 1-thioethyl, 1-thio-isopropyl, 1-thio-n-propyl1-thio-isobutyl, 1-thio-n-butyl or 1-thio-tert-butyl.

Aryloxy or heteroaryloxy having 5 to 40 aromatic ring atoms denotes O-aryl or O-heteroaryl and refers to aryl or heteroaryl, respectively, bonded via an oxygen atom.

Aralkyl or heteroaralkyl having 5 to 40 aromatic ring atoms means that the alkyl group is substituted with an aryl or heteroaryl group as described above.

For the present invention, a phosphorescent emitter is a compound that exhibits light emission from an excited state having relatively high spin multiplicities (i.e., spin state >1), particularly from an excited triplet state. For the purposes of the present application, all luminescent complexes comprising transition metals or lanthanides are considered phosphorescent emitters. A more precise definition is given below.

If a composition comprising at least one compound of formula (1) as described above or preferably as described below and at least one compound of formula (2) as described above or as described below is used as matrix material for a phosphorescent emitter, its triplet energy is preferably not significantly less than the triplet energy of the phosphorescent emitter. The following preferably applies to the triplet energy level: t is₁(luminophores) -T₁(substrate) 0.2eV or less, particularly preferably 0.15eV or less, very particularly preferably 0.1eV or less. Here T₁(host) is the triplet energy level of the host material in the light-emitting layer, this condition applies to each of the two host materials, and T₁(emitter) is the triplet energy level of a phosphorescent emitter. If the light-emitting layer comprises more than two host materials, the above relationship preferably also applies to each further host material.

In a preferred embodiment of the invention, compounds of the following formula (1) are selected in which up to 4 variables X, preferably up to 3 variables X, particularly preferably 2 variables X, very particularly preferably 1 variable X, represents N and the remaining variables X represent CR.

In a preferred embodiment of the invention, compounds of the following formula (1) are selected in which all variables X denote CR, where R in each case, i.e. independently at each occurrence, has the abovementioned meaning. These compounds are described by the formula (1a),

wherein R, V and v have the meanings specified above or preferably the meanings specified below.

The invention therefore also relates to a composition as described above, in which the compound of formula (1) corresponds to the compound of formula (1a),

wherein R, V and v have the meanings specified above or preferably the meanings specified below.

R is selected, identically or differently on each occurrence, from H, D, F, Cl, Br, I, CN, NO₂，N(Ar)₂，N(R²)₂，C(＝O)Ar，C(＝O)R²，P(＝O)(Ar)₂，P(Ar)₂，B(Ar)₂，Si(Ar)₃，Si(R²)₃Straight-chain alkyl, alkoxy or thioalkyl having 1 to 20C atoms or branched or cyclic alkyl, alkoxy or thioalkyl having 3 to 20C atoms or alkenyl having 2 to 20C atoms, which may in each case be substituted by one or more radicals R²Substitution of one or more non-adjacent CH₂The group can be represented by R²C＝CR²、Si(R²)₂、C＝O、C＝S、C＝NR²、P(＝O)(R²)、SO、SO₂、NR²O, S or CONR²And wherein one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂Instead, aromatic or heteroaromatic ring systems having from 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R²Substituted, or aryloxy or heteroaryloxy having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substituted, or aralkyl or heteroaralkyl having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substitution; two radicals bound to the same carbon atom or to adjacent carbon atomsThe substituents R may optionally form mono-or polycyclic aliphatic, aromatic or heteroaromatic ring systems which may be interrupted by one or more radicals R²And (4) substitution.

In one embodiment of the present invention, preference is given to selecting compounds of the following formula (1) or (1a), in which V and V have the meanings given above and 1,2,3 or 4 substituents R, preferably 1,2 or 3 substituents R, particularly preferably 2,3 or 4 substituents R, very particularly preferably 2 substituents R, are not H but have the meanings described below as preferred.

Preferred substituents R of the compounds of the formula (1) or of the formula (1a) in the abovementioned number, which are not H, preferably denote straight-chain alkyl, alkoxy or thioalkyl having 1 to 20C atoms or branched or cyclic alkyl, alkoxy or thioalkyl having 3 to 20C atoms, alkenyl having 2 to 20C atoms, which may in each case be substituted by one or more radicals R²Substituted, aromatic or heteroaromatic ring systems having 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R²Substituted, or aryloxy or heteroaryloxy having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substituted, or aralkyl or heteroaralkyl having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substitution; two substituents R which are bonded to the same carbon atom or to adjacent carbon atoms may form a mono-or polycyclic aliphatic, aromatic or heteroaromatic ring system which may be interrupted by one or more radicals R²And (4) substitution.

The abovementioned number of particularly preferred substituents R other than H of the compounds of the formula (1) or of the formula (1a) preferably denotes aromatic or heteroaromatic ring systems having from 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R²Substitution; two substituents R which are bonded to the same carbon atom or to adjacent carbon atoms may form a mono-or polycyclic aliphatic, aromatic or heteroaromatic ring system which may be interrupted by one or more radicals R²And (4) substitution.

Two substituents which are adjacent in each case on the same ring of the lactam skeleton or on different rings of the lactam skeleton in the compounds of the formula (1) or (1a)R particularly preferably forms the following radicals (S1) to (S12), where # and # denote and form a radical which may be substituted by one or more radicals R²The corresponding attachment site for the C atom of a substituted mono-or polycyclic aliphatic, aromatic or heteroaromatic ring system:

r in the (S1) to (S12) moieties²Preferably H or an aromatic or heteroaromatic ring system having 5 to 40 ring atoms which may be substituted by R³Substitution, preferably is H or phenyl.

Very particularly preferred substituents R of the compounds of the formula (1) or of the formula (1a) in the abovementioned number of radicals other than H denote aromatic or heteroaromatic ring systems having from 5 to 40 ring atoms which may be substituted by one or more radicals R³Substituted, or preferably selected from the ring systems Ar-1 to Ar-22,

wherein Y is³O, NR being represented identically or differently at each occurrence^#S or C (R)^#)₂Wherein the group R is bonded to N^#Is not equal to H, and R³Have the above meanings or the following preferred meanings, and the dotted bond represents a bond with the C atom bearing the corresponding substituent R.

Radical R^#At each occurrence, identically or differently, selected from H, D, F, Cl, Br, I, CN, NO₂，N(Ar)₂，N(R²)₂，C(＝O)Ar，C(＝O)R²，P(＝O)(Ar)₂，P(Ar)₂，B(Ar)₂，Si(Ar)₃，Si(R²)₃Straight-chain alkyl, alkoxy or thioalkyl having 1 to 20C atoms or branched or cyclic alkyl, alkoxy or thioalkyl having 3 to 20C atoms or alkenyl having 2 to 20C atoms, which may in each case be substituted by one or more radicals R²Substitution of one or more non-adjacent CH₂The group can be represented by R²C＝CR²、Si(R²)₂、C＝O、C＝S、C＝NR²、P(＝O)(R²)、SO、SO₂、NR²O, S or CONR²And wherein one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂Instead, aromatic or heteroaromatic ring systems having from 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R²Substituted, or aryloxy or heteroaryloxy having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substituted, or aralkyl or heteroaralkyl having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²Substitution; two substituents R bound to the same carbon atom or to adjacent carbon atoms^#May optionally form a mono-or polycyclic aliphatic, aromatic or heteroaromatic ring system which may be substituted by one or more radicals R²And (4) substitution.

Y³Preferably O, S or C (CH)₃)₂。Y³O is particularly preferred.

Substituent R in structures Ar-1 through Ar-22³Selected, identically or differently on each occurrence, from H, D, F, CN, aliphatic hydrocarbon radicals having 1 to 20C atoms or aromatic or heteroaromatic ring systems having 6 to 30 aromatic ring atoms, where one or more H atoms may be replaced by D, F, Cl, Br, I or CN and which may be substituted by one or more alkyl radicals each having 1 to 4 carbon atoms; two or more adjacent substituents R³May form a monocyclic or polycyclic aliphatic ring system with each other. Substituent R in structures Ar-1 through Ar-22³Preferably the same or different at each occurrenceSelected from H, F, CN, aliphatic hydrocarbon radicals having 1 to 10C atoms or aromatic or heteroaromatic ring systems having 5 to 30 aromatic ring atoms. Substituent R in structures Ar-1 through Ar-22³Preferably selected, identically or differently at each occurrence, from H or an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms as described above, but preferably dibenzofuran, dibenzothiophene, 9-phenylcarbazole or spirobifluorene.

Particular preference is given to 1,2 or 3 substituents R, very particular preference to 2 substituents R, meaning Ar-1 to Ar-7, where R³The meanings given above or preferred.

In the compounds of the formula (1) or (1a) or the compounds of the formula (1) or (1a) described as preferred, v is preferably 0, which corresponds to the formula (1b),

wherein R independently at each occurrence has the meaning specified or designated as preferred above.

In the compounds of the formula (1) or (1a) or the preferably described compounds of the formula (1) or (1a), V is preferably 1 and V represents a single bond, which corresponds to the formula (1c),

wherein R independently at each occurrence has the meaning specified or designated as preferred above.

In the compounds of formula (1) or (1a) or the compounds of formula (1) or (1a) preferably described, V is preferably 1, V represents a single bond, and the two substituents R represent a moiety of formula (S1), which corresponds to formula (1d),

wherein R and R²Independently at each occurrence has the meaning specified above or preferred.

In the compounds of the formula (1) or (1a) or the compounds of the formula (1) or (1a) described as preferred, vYisIs selected as 1, and V represents C (R)⁰)₂O or S, which corresponds to formula (1e),

wherein R independently at each occurrence has the meaning specified or designated as preferred above. V is particularly preferably C (R)⁰)₂Wherein R is⁰In each case independently of one another, have the meanings given above.

Particularly preferred compounds of formula (1b) are compounds of formula (1f),

wherein R independently at each occurrence has the meaning specified or designated as preferred above.

Particularly preferred compounds of formula (1c) are compounds of formula (1g),

wherein R independently at each occurrence has the meaning specified or designated as preferred above.

Very particular preference is given to selecting, for the compositions according to the invention, the compounds of formulae (1c) and (1g) as described above, or compounds having the preferred substituents R as described above.

Particularly preferred compounds of formula (1d) are compounds of formula (1h),

wherein R independently at each occurrence has the meaning specified or designated as preferred above.

Particularly preferred compounds of formula (1e) are compounds of formula (1i),

wherein R independently at each occurrence has the meaning specified or designated as preferred above.

Examples of suitable compounds of formula (1), (1a), (1b), (1c), (1d), (1e), (1f), (1g), (1h) or (1i) selected according to the invention are the structures given in table 1 below.

Table 1:

particularly suitable compounds of the formula (1), (1a), (1b), (1c), (1d), (1e), (1f), (1g), (1h) or (1i) selected according to the invention are the compounds L1 to L34, very particularly preferably the compounds L1 to L16, in table 2.

TABLE 2

The preparation of compounds of formula (1) or preferably of compounds of formulae (1a) to (1i) and compounds L1 to L34 is known to the person skilled in the art. The compounds can be prepared by synthetic procedures known to those skilled in the art, such as halogenation, preferably bromination, and subsequent organometallic coupling reactions, such as Suzuki coupling, Heck coupling or Hartwig-Buchwald coupling. The preparation of the compounds of the formula (1) or preferably of the compounds of the formulae (1a) to (1i) and of the compounds L1 to L34 is known, in particular, from the synthesis examples on pages 42 to 46 and 48 to 64 of WO2011/137951, from the synthesis examples on pages 44 to 67 of WO2013/064206 or from pages 54 to 67 of WO 2014/094964.

In one embodiment of the invention, the compound of formula (2) as described above is selected for use in a composition with the compounds of formulae (1), (1a), (1b), (1c), (1d), (1e), (1f), (1g), (1h) and (1i) described or preferably described above, or with compounds L1 to L34.

Symbol X in the Compound of formula (2)²Preferably twice, particularly preferably once, N, the remainder of the groups X²Represents CR¹Wherein R is¹In each case independently of one another, have the meaning specified above or preferably below.

X in the Compound of formula (2)²Very particularly preferably CR¹Wherein R is¹Independently at each occurrence has the meaning specified above or below.

Wherein X²Representing CR identically or differently at each occurrence¹The compound of formula (2) is represented by formula (2a),

wherein R is¹、Ar₁And Ar₂Have the meanings given above or the preferred meanings described below, and q and t in each case independently of one another denote 0, 1,2,3 or 4, r and s in each case independently of one another denote 0, 1,2 or 3.

In the compounds of formula (2a), the substituent R¹Does not include H. This exclusion term applies accordingly to all formulae below where q, t, s and r appear.

The present invention therefore also relates to a composition as described above, in which the compound of formula (2) corresponds to the compound of formula (2 a).

In a preferred embodiment of the compounds of the formula (2) or (2a), two carbazoles are in each case attached to one another at position 3. This embodiment is represented by the compound of formula (2b),

wherein R is¹、Ar₁And Ar₂Have the meanings given above or the preferred meanings described below, and q and t are as defined inIn each case independently of one another denotes 0, 1,2,3 or 4, and r and s in each case independently of one another denote 0, 1,2 or 3.

The present invention therefore also relates to a composition as described above, in which the compound of formula (2) corresponds to the compound of formula (2 b).

Z is preferably C (R)⁰)₂O or S. R in Z⁰Methyl, ethyl or n-butyl is preferred, and methyl is particularly preferred.

In the compounds of the formula (2), (2a) or (2b), Z is particularly preferably C (R)⁰)₂。

In the compounds of formula (2), (2a) or (2b) as described or preferred above, n is preferably 0. This embodiment is represented by the compound of formula (2c),

In the compounds of formula (2), (2a), (2b) or (2c), q is preferably 0, 1 or 2, wherein R¹Have the meaning specified above or the meaning specified below. q is particularly preferably 0 or 1. q is very particularly preferably 0.

If in the compounds of the formula (2), (2a), (2b) or (2c) q is greater than 0, then the substituent R¹Preferably selected, identically or differently on each occurrence, from D, F, alkyl having 1 to 40C atoms or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²And (4) substitution. This R¹The aromatic or heteroaromatic ring systems having from 5 to 40 aromatic ring atoms in (A) are preferably derived from benzene, dibenzofuran, dibenzothiophene, 9-phenylcarbazole, biphenyl or terphenyl, which may be substituted by one or more radicals R²And (4) substitution. Substituent group [ R¹]_qIs 1,2,3 or 4 bits or a group of 1 and 4 bitsAnd combinations of 1 and 3 positions, particularly preferably 1 and 3, 2 or 3, very particularly preferably 3, where R is¹Has one of the preferred meanings specified above, and q is greater than 0. [ R ]¹]_qParticularly preferred substituents R in¹Are phenyl and biphenyl.

In the compounds of formula (2), (2a), (2b) or (2c), R is preferably 0, 1 or 2, wherein R is¹Have the meaning specified above or the meaning specified below. r is particularly preferably 0 or 1, very particularly preferably 0.

If R is greater than 0 in the compounds of the formula (2), (2a), (2b) or (2c), the substituent R¹Preferably selected, identically or differently at each occurrence, from D, F, alkyl having 1 to 40C atoms or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²And (4) substitution. This R¹The aromatic or heteroaromatic ring systems having from 5 to 40 aromatic ring atoms in (A) are preferably derived from benzene, dibenzofuran, dibenzothiophene, 9-phenylcarbazole, biphenyl and terphenyl, which may be substituted by one or more radicals R²And (4) substitution. Substituent group [ R¹]_rIs the 1-or 2-position, particularly preferably the 1-position, where R is¹Has one of the preferred meanings mentioned above, and r is greater than 0. [ R ]¹]_rParticularly preferred substituents R in¹Are phenyl, 9-phenylcarbazole and 9H-carbazol-9-yl.

In the compounds of formula (2), (2a), (2b) or (2c), s is preferably 0, 1 or 2, wherein R¹Have the meaning specified above or the meaning specified below. s is particularly preferably 0 or 1, very particularly preferably 0.

If s is greater than 0 in the compounds of the formula (2), (2a), (2b) or (2c), the substituent R¹Preferably selected, identically or differently at each occurrence, from D, F, alkyl having 1 to 40C atoms or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²And (4) substitution. This R¹The aromatic or heteroaromatic ring systems having from 5 to 40 aromatic ring atoms in (A) are preferably derived from benzene, dibenzofuran, dibenzothiophene, 9-phenylcarbazole, biphenyl or trisBiphenyl, which may be substituted by one or more radicals R²And (4) substitution. Substituent group [ R¹]_sIs the 1-or 2-position, particularly preferably the 1-position, where R is¹Has one of the preferred meanings specified above, and s is greater than 0. [ R ]¹]_rParticularly preferred substituents R in¹Are phenyl, 9-phenylcarbazole and 9H-carbazol-9-yl.

In the compounds of formula (2), (2a), (2b) or (2c), t is preferably 0, 1 or 2, wherein R¹Have the meaning specified above or the meaning specified below. t is particularly preferably 0 or 1. t is very particularly preferably 0.

If t is greater than 0 in the compound of formula (2), (2a), (2b) or (2c), the substituent R¹Preferably selected, identically or differently at each occurrence, from D, F, alkyl having 1 to 40C atoms or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²And (4) substitution. This R¹The aromatic or heteroaromatic ring systems having from 5 to 40 aromatic ring atoms in (A) are preferably derived from benzene, dibenzofuran, dibenzothiophene, 9-phenylcarbazole, biphenyl or terphenyl, which may be substituted by one or more radicals R²And (4) substitution. Substituent group [ R¹]_qAre preferably 1,2,3 or 4 or a combination of 1 and 4, 1 and 3, 1 and 2 and 3 and 4, particularly preferably 1 and 3, 2 or 3, very particularly preferably 2 or 3, where R is¹Has one of the preferred meanings mentioned above, and t is greater than 0. [ R ]¹]_tParticularly preferred substituents R in¹Phenyl, biphenyl and terphenyl.

Substituent R²Preferably identically or differently selected in each occurrence from D, F, Cl, Br, I, CN, NO₂，N(Ar)₂，NH₂，N(R³)₂，C(＝O)Ar，C(＝O)H，C(＝O)R³，P(＝O)(Ar)₂Straight-chain alkyl, alkoxy or thioalkyl having 1 to 40C atoms or branched or cyclic alkyl, alkoxy or thioalkyl having 3 to 40C atoms or alkenyl or alkynyl having 2 to 40C atoms, which may in each case be substituted by one or moreRadical R³Substituted or aromatic or heteroaromatic ring systems having from 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R³Substituted or aryloxy or heteroaryloxy having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R³And (4) substitution. Substituent R²Particular preference is given in the case of aromatic or heteroaromatic ring systems as described above, preferably selected from carbazole, 9-phenylcarbazole, dibenzofuran, dibenzothiophene, fluorene, terphenyl or spirobifluorene, very particularly preferably derived from dibenzofuran.

At one substituent R as described above²By a substituent R³In the case of substitution, R as described above or as described in preference applies³The meaning of (a).

In the compounds of formula (2), (2a), (2b) or (2c) as described above, Ar₁And Ar₂In each case independently of one another, is an aromatic ring system having 6 to 40 aromatic ring atoms or a heteroaromatic ring system having 10 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³And (4) substitution. Due to the para-group R¹And R³The composition according to the invention differs from the composition of the light-emitting layer in the examples of WO2013/064206 and WO 2014/094964 by the specified definition.

In the presence of one or more substituents R³In the case of substituted heteroaromatic ring systems having 10 to 40C atoms, particular preference is given to electron-rich ring systems in which R is optionally substituted³The substituted ring systems preferably contain only one N atom in total, or are optionally substituted by R³The substituted ring systems contain in total one or more O and/or S atoms.

In the compounds of the formula (2), (2a), (2b) or (2c) or the compounds of the formulae (2), (2a), (2b) or (2c) described as preferred, Ar₁And Ar₂Preferably selected from the aromatic or heteroaromatic ring systems Ar-1 to Ar-22 as described above, in which in respect of the radical R^#、Y³And R³The remarks made above also apply, preferably to the case where R is optionally substituted as represented by Ar-12, Ar-13, Ar-14, Ar-15, Ar-20 and Ar-21³Substituted heteroaromatic ring systems contain only one N atom in total.

In a preferred embodiment of the invention, compounds of formula (2), (2a), (2b) or (2c) are selected in which the substituent Ar₁And Ar₂One of them denotes an aromatic ring system having 6 to 40 aromatic ring atoms or a heteroaromatic ring system having 10 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³Substituted, the other substituent denotes an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³And (4) substitution.

The invention therefore also relates to a composition as described or preferred above, in which the substituents Ar in the compounds of the formulae (2) or (2a) or (2b) or (2c)₁And Ar₂One of them denotes an aromatic ring system having 6 to 40 aromatic ring atoms or a heteroaromatic ring system having 10 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³Substituted, the other substituent denotes an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³And (4) substitution.

In this embodiment, preferably, one substituent Ar is as described above or as preferred₁Or Ar₂Corresponding to one of the structures Ar-1 to Ar-22 and the other substituent corresponding to one of the structures Ar-1 to Ar-11 or Ar-16 to Ar-19 or Ar-22, preferably in the presence of a substituent represented by Ar-12, Ar-13, Ar-14, Ar-15, Ar-20 and Ar-21 optionally substituted by R³Substituted heteroaromatic ring systems contain only one N atom in total.

In a particularly preferred embodiment of the invention, compounds of the formula (2), (2a), (2b) or (2c) are selected in which the substituent Ar₁Or Ar₂In each case independently of one another denotes an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³And (4) substitution.

When present in this embodiment, the substituent R³Preferably aromatic, and if Ar₁And Ar₂Denotes an aromatic ring system having 6 to 40 ring atoms, then R³Containing no heteroatoms.

The invention therefore also relates to a composition as described or preferably described aboveWherein Ar represents a substituent in the compound of formula (2) or (2a) or (2b) or (2c)₁And Ar₂In each case independently of one another denotes an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³And (4) substitution.

In this embodiment, it is preferred that the substituent Ar is as described above or as described as preferred₁And Ar₂In each case independently of one another correspond to one of the structures Ar-1 to Ar-11 or Ar-16 to Ar-19 or Ar-22, preferably optionally substituted by R³Substituents R in substituted aromatic ring systems³Under conditions selected such that they do not contain heteroatoms.

Examples of suitable compounds of formula (2), (2a), (2b) or (2c) selected according to the present invention are the structures shown in table 3 below.

Table 3:

particularly suitable examples of compounds of formula (2), (2a), (2B) or (2c) selected according to the invention are compounds B1 to B14 as described above.

The preparation of compounds of formula (2) or of the preferred compounds of formulae (2a), (2b) and (2c) and of the compounds of Table 3 is known to the person skilled in the art from the literature. The compounds can be prepared by synthetic procedures known to those skilled in the art, such as halogenation, preferably bromination, and subsequent organometallic coupling reactions, such as Suzuki coupling, Heck coupling or Hartwig-Buchwald coupling. Certain biscarbazoles of formula (2) are commercially available.

The compounds of formula (2) or preferred compounds of formulae (2a), (2b) and (2c) wherein n represents 0 may be prepared, for example, according to scheme 1 or scheme 2.

Scheme 1 for the preparation of asymmetric biscarbazoles of formula (2), (2a), (2b) or (2c), wherein n represents 0:

scheme 2 for the preparation of symmetrical biscarbazoles (Ar) of formula (2), (2a), (2b) or (2c)₁And Ar₂Identical and abbreviated in the schemes as Ar₁) Wherein n represents 0:

scheme 3 for the preparation of biscarbazoles of formula (2), (2a), (2b) or (2c), wherein n represents 1:

more detailed information on the synthesis and more literature citations are described in the experimental part.

The host materials of the above formulae (1) and (1a) to (1i) and the preferably described embodiments thereof or the compounds of tables 1 and 2 can be combined according to the invention as desired with the host materials of the formulae (2), (2a), (2b) and (2c) and the preferably described embodiments thereof or the compounds of table 3.

For the compositions of the present invention, particularly preferred mixtures of host materials of formula (1) with host materials of formula (2) are obtained by combining compounds L1 to L34 of table 2 with compounds of table 3.

A very particularly preferred mixture of host materials of formula (1) and of formula (2) is obtained by combining each of the compounds L1 to L34 of table 2 with the compounds B1 to B14 of table 3.

Very particularly preferred mixtures M1 to M224 of host materials of formula (1) and of host materials of formula (2) are obtained by combining compounds L1 to L16 of table 2 with compounds B1 to B14 of table 3, as shown in table 4 below.

Table 4:

in the composition according to the invention, the concentration of electron transport hosts of formula (1) as described or preferred above is in the range of from 5 to 90 wt. -%, preferably in the range of from 10 to 85 wt. -%, more preferably in the range of from 20 to 85 wt. -%, even more preferably in the range of from 30 to 80 wt. -%, very particularly preferably in the range of from 20 to 60 wt. -%, most preferably in the range of from 30 to 50 wt. -%, based on the total composition.

The concentration of the hole-transporting host of formula (2) as described or preferred above in the composition is in the range of 10 to 95 wt.%, preferably in the range of 15 to 90 wt.%, more preferably in the range of 15 to 80 wt.%, even more preferably in the range of 20 to 70 wt.%, very particularly preferably in the range of 40 to 80 wt.%, most preferably in the range of 50 to 70 wt.%, based on the total composition.

In another preferred embodiment, the composition according to the invention may comprise further compounds, in particular organic functional materials, in addition to at least one compound of formula (1) as described or preferred above as electron-transporting host or electron-transporting matrix material and at least one compound of formula (2) as described or preferred above as hole-transporting host or hole-transporting matrix material. The composition of this embodiment preferably forms an organic layer in an electronic device, as described below.

The present invention therefore also relates to a composition comprising, in addition to the above-mentioned materials, at least one further compound chosen from: hole injection materials, hole transport materials, hole blocking materials, wide band gap materials, fluorescent emitters, phosphorescent emitters, host materials, electron blocking materials, electron transport materials, and electron injection materials, n-type dopants, and p-type dopants. The person skilled in the art has no difficulty at all in selecting these materials from the numerous materials known.

The n-type dopant herein refers to a reducing agent, i.e., an electron donor. Preferred examples of the n-type dopant are W (hpp)₄And other electron-rich metal complexes according to WO 2005/086251 a2, P ═ N compounds (e.g. WO 2012/175535 a1, WO 2012/175219 a1), naphthalene carbodiimides (e.g. WO 2012/168358 a1), fluorenes (e.g. WO 2012/031735a1), free and diradicals (e.g. EP 1837926 a1, WO 2007/107306 a1), pyridines (e.g. EP 2452946a1, EP 2463927 a1), N-heterocyclic compounds (e.g. WO 2009/000237 a1) and acridines and phenazines (e.g. US2007/145355 a 1).

A p-type dopant herein refers to an oxidizing agent, i.e., an electron acceptor. A preferred example of a p-type dopant is F₄-TCNQ、F₆TNAP, NDP-2(Novaled), NDP-9(Novaled), quinones (e.g. EP 1538684 a1, WO 2006/081780 a1, WO 2009/003455 a1, WO 2010/097433 a1), axines (e.g. EP 1988587 a1, US 2010/102709a1, EP 2180029 a1, WO 2011/131185 a1, WO 2011134458 a1, US 2012/223296 a1), S-containing transition metal complexes (e.g. WO 2007/134873 a1, WO 2008/061517 a2, WO 2008/061518 a2, DE102008051737 a1, WO 2009/089821 a1, US 2010/096600 a1), bisimidazoles (e.g. WO 2008/138580 a1), phthalocyanines (e.g. WO 2008/058525 a2), boratetracazapentanes (e.g. WO 2007/115540 a1), fullerenes (e.g. DE 102010046040 a1) and main group halides (e.g. WO 2008/128519 a 2).

A wide bandgap material in the sense of the disclosure of US 7,294,849 is herein meant a material which is characterized by a bandgap of at least 3.5eV, where bandgap refers to the separation between the HOMO and LUMO energies of the material.

The composition according to the invention comprising a ambipolar host and an electron transporting host preferably additionally comprises at least one luminescent compound or emitter, wherein phosphorescent emitters are particularly preferred.

The term phosphorescent emitter generally includes compounds in which light is emitted by spin-forbidden transitions from an excited state with a relatively high spin-multiplicities (i.e. spin state >1), for example by transitions from a triplet state or a state with an even higher spin quantum number (e.g. a quintet state). This preferably means a transition from the triplet state.

Suitable phosphorescent emitters (═ triplet emitters) are in particular compounds which emit light under suitable excitation, preferably in the visible region, and which also comprise at least one atom having an atomic number of greater than 20, preferably greater than 38 and less than 84, particularly preferably greater than 56 and less than 80, in particular metals having this atomic number. The phosphorescent emitters used are preferably compounds containing copper, molybdenum, tungsten, rhenium, ruthenium, osmium, rhodium, iridium, palladium, platinum, silver, gold or europium, in particular compounds containing iridium or platinum. For the purposes of the present invention, all luminescent compounds comprising the above-mentioned metals are considered phosphorescent emitters.

In general, suitable phosphorescent complexes are all those which are used in accordance with the prior art for phosphorescent OLEDs and are known to the person skilled in the art of organic electroluminescent devices.

The following applications disclose examples of the described luminaries: WO 2016/015815, WO 00/70655, WO2001/41512, WO 2002/02714, WO 2002/15645, EP 1191613, EP 1191612, EP 1191614, WO05/033244, WO 05/019373, US 2005/0258742, WO 2009/146770, WO 2010/015307, WO 2010/031485, WO 2010/054731, WO 2010/054728, WO 2010/086089, WO 2010/099852, WO 2010/102709, WO 2011/032626, WO 2011/066898, WO 2011/157339, WO 2012/007086, WO 2014/008982, WO 2014/023377, WO 2014/094961, WO 2014/094960, WO 2015/036074, WO 2015/104045, WO 2015/117718, WO 2016/015815, WO 2016/124304, WO 2017/032439, WO 2015/036074, WO 2015/117718 and WO 2016/015815.

Preferred examples of phosphorescent emitters are shown in table 5 below.

Table 5:

preferred examples of phosphorescent polypod emitters are shown in table 6 below.

Table 6:

in the compositions according to the invention, the respective mixtures M1, M, M121, M122, M123, M124, M125, M126, M127, M128, M129, M130, M131, M132, M133, M134, M135, M136, M137, M138, M139, M140, M141, M142, M143, M144, M145, M146, M147, M148, M149, M150, M151, M152, M153, M154, M155, M156, M157, M158, M159, M160, M161, M162, M163, M164, M165, M166, M167, M168, M169, M170, M171, M172, M173, M174, M175, M176, M177, M178, M179, M180, M181, M182, M183, M185, M187, M188, M189, M190, M191, M192, M193, M194, M198, M220, M213, M220, M213, M185, M213.

The compositions according to the invention comprising at least one phosphorescent emitter preferably form an infrared, yellow, orange, red, green, blue or ultraviolet-emitting layer, particularly preferably a yellow or green-emitting layer and very particularly preferably a green-emitting layer.

The yellow light-emitting layer herein refers to a layer having a photoluminescence peak in the range of 540nm to 570 nm. The orange light emitting layer refers to a layer having a photoluminescence peak in the range of 570nm to 600 nm. The red light-emitting layer refers to a layer having a photoluminescence peak in the range of 600nm to 750 nm. The green light-emitting layer refers to a layer having a photoluminescence peak in the range of 490nm to 540 nm. The blue light emitting layer refers to a layer having a photoluminescence peak in the range of 440nm to 490 nm. The photoluminescence of the layer is determined here by measuring the photoluminescence spectrum of a layer having a layer thickness of 50nm at room temperature, wherein said layer comprises a composition according to the invention, i.e. comprising a luminophore and a matrix.

For example, the photoluminescence spectrum of the layer was recorded using a commercially available photoluminescence spectrometer.

Is generally at 10^-5Measuring photoluminescence spectra of selected luminophores in an oxygen-free solution at molar concentrations, wherein the measurements are carried out at room temperatureAny solvent in which the selected luminophore is dissolved at the concentration is suitable. Particularly suitable solvents are usually toluene or 2-methyl-THF, and also dichloromethane. Measurements were performed using a commercially available photoluminescence spectrometer. Triplet energy T₁Determined (in eV) from the photoluminescence spectrum of the luminophore. First, the maximum peak value Plmax (in nm) of the photoluminescence spectrum is determined. The maximum peak value Plmax (in nm) was then converted to eV according to E (T1(eV)) ═ 1240/E (T1(nm)) ═ 1240/Plmax (nm)).

Thus, preferred phosphorescent emitters are infrared emitters, preferably from table 5 or table 6, which have triplet energies T₁Preferably from about 1.9eV to about 1.0 eV.

Thus, preferred phosphorescent emitters are red emitters, preferably from table 5 or table 6, whose triplet energies T₁Preferably from about 2.1eV to about 1.9 eV.

Preferred phosphorescent emitters are therefore yellow emitters, preferably from Table 5 or 6, whose triplet energy T is₁Preferably from about 2.3eV to about 2.1 eV.

Thus, preferred phosphorescent emitters are green emitters, preferably from table 5 or table 6, with triplet energies T₁Preferably from about 2.5eV to about 2.3 eV.

Thus, preferred phosphorescent emitters are blue emitters, preferably from table 5 or table 6, which have triplet energies T₁Preferably from about 3.1eV to about 2.5 eV.

Preferred phosphorescent emitters are therefore UV emitters, preferably from Table 5 or 6, whose triplet energy T is₁Preferably from about 4.0eV to about 3.1 eV.

Thus, particularly preferred phosphorescent emitters are green or yellow emitters as described above, preferably from table 5 or 6.

Very particularly preferred phosphorescent emitters are therefore green emitters, preferably from Table 5 or 6, whose triplet energy T is₁Preferably from about 2.5eV to about 2.3 eV.

As mentioned above, the green emitters preferably from table 5 or 6 are very particularly preferably selected for the composition according to the invention or the light-emitting layer according to the invention.

Preferred fluorescent emitters are selected from the class of arylamines. For the purposes of the present invention, arylamine or aromatic amine means a compound comprising three substituted or unsubstituted aromatic or heteroaromatic ring systems bonded directly to nitrogen. At least one of these aromatic or heteroaromatic ring systems is preferably a fused ring system, particularly preferably having at least 14 aromatic ring atoms. Preferred examples thereof are aromatic anthracenediamines, aromatic pyreneamines, aromatic pyrenediamines, aromatic chicory amines or aromatic chicory diamines. Aromatic anthracenamines are understood to mean compounds in which one diarylamino group is bonded directly to the anthracenyl group, preferably in the 9-position. Aromatic anthracenediamines are understood to mean compounds in which two diarylamino groups are bonded directly to the anthracene group, preferably in the 9, 10-position. Aromatic pyrene amines, aromatic pyrene diamines, aromatic chicory amines or aromatic chicory diamines are defined analogously thereto, wherein the diarylamino groups are preferably bonded to pyrene in the 1-position or in the 1, 6-position. Also preferred fluorescent emitters are indenofluoreneamines or indenofluorenylamines, e.g. according to WO 2006/108497 or WO 2006/122630, benzindenofluoreneamines or benzindenofluorenyldiamines, e.g. according to WO 2008/006449, and dibenzoindenofluorenylamines or dibenzoindenofluorenyldiamines, e.g. according to WO 2007/140847, and indenofluorene derivatives containing fused aryl groups, as disclosed in WO 2010/012328.

In another preferred embodiment of the present invention, the composition according to the invention is used as a component of a mixed matrix system. The mixed matrix system preferably comprises three or four different matrix materials, particularly preferably three different matrix materials (i.e. other matrix components than the composition according to the invention). Particularly suitable matrix materials which can be used as matrix component of the mixed matrix system in combination with the composition according to the invention are selected from wide band gap materials, Electron Transport Materials (ETM) and Hole Transport Materials (HTM).

The mixed matrix system is preferably used in phosphorescent organic electroluminescent devices. More precise details on mixed matrix systems are given in particular in application WO 2010/108579. Particularly suitable matrix materials which can be used in combination with the compositions according to the invention as matrix components of mixed matrix systems in phosphorescent or fluorescent organic electroluminescent devices are selected from the following preferred matrix materials indicated for phosphorescent emitters or preferred matrix materials indicated for fluorescent emitters, depending on the type of emitter used. The mixed matrix system is preferably optimized for the luminophores in table 5 or 6.

In addition to the compositions according to the invention as described above, suitable further host materials, preferably for fluorescent emitters, particularly preferably mixtures comprising materials from the group of M1 to M224, are substances of various classes. Preferred additional host materials are selected from the following classes: oligomeric aromatic subunits (e.g. 2,2',7,7' -tetraphenylspirobifluorene according to EP676461, or dinaphthylanthracene), in particular oligomeric aromatic subunits containing fused aromatic groups, oligomeric aromatic subunits vinylidenes (e.g. DPVBi or spiro-DPVBi according to EP 676461), polypentametal complexes (e.g. according to WO 2004/081017), hole-conducting compounds (e.g. according to WO 2004/058911), electron-conducting compounds, in particular ketones, phosphine oxides, sulfoxides and the like (e.g. according to WO2005/084081 and WO 2005/084082), atropisomers (e.g. according to WO 2006/048268), boronic acid derivatives (e.g. according to WO 2006/117052) or benzanthracenes (e.g. according to WO 2008/145239). Particularly preferred matrix materials are selected from the following classes: oligomeric aromatic subunits including naphthalene, anthracene, benzanthracene and/or pyrene, or atropisomers of these compounds, oligomeric aromatic subunits vinyl, ketones, phosphine oxides and sulfoxides. Very particularly preferred matrix materials are selected from the class of oligomeric aromatic subunits, including anthracenes, benzanthracenes, triphenylenes and/or pyrenes, or atropisomers of these compounds. For the purposes of the present invention, oligomeric arylidene is understood to mean a compound in which at least three aryl or arylidene groups are bonded to one another.

In addition to the compositions according to the invention as described above, suitable further matrix materials, preferably for phosphorescent emitters, particularly preferably mixtures comprising materials from the group of M1 to M224, are substances of various classes. Preferred other matrix materials are selected from the following classes: aromatic amines, in particular triarylamines (for example according to U.S. Pat. No. 5, 2005/0069729), carbazole derivatives (for example CBP, N, N-biscarbazolylbiphenyl) or compounds according to WO 2005/039246, U.S. Pat. No. 3, 2005/0069729, JP 2004/288381, EP 1205527 or WO 2008/086851, bridged carbazole derivatives (for example according to WO 2011/088877 and WO 2011/128017), indenocarbazole derivatives (for example according to WO 2010/136109 and WO 2011/000455), azacarbazole derivatives (for example according to EP 1617710, EP 1617711, EP 1731584, JP 2005/347160), indolocarbazole derivatives (for example according to WO 2007/063754 or WO2008/056746), ketones (for example according to WO 2004/093207 or WO 2010/006680), phosphine oxides, sulfoxides and sulfones (for example according to WO 2005/003253), oligophenylenes, bipolar matrix materials (e.g. according to WO 2007/137725), silanes (e.g. according to WO 2005/111172), borazahydes or borates (e.g. according to WO 2006/117052), triazine derivatives (e.g. according to WO 2010/015306, WO 2007/063754 or WO2008/056746), zinc complexes (e.g. according to EP 652273 or WO 2009/062578), aluminum complexes (e.g. BAlq), sildiazacyclorac and siltetraazazerac derivatives (e.g. according to WO 2010/054729), phosphodiazacyclorac derivatives (e.g. according to WO 2010/054730), and aluminum complexes (e.g. BAlq).

According to an alternative embodiment of the present invention, the composition does not comprise other components, i.e. functional materials, than the components of the electron transporting host and the hole transporting host.

The invention therefore also relates to a composition consisting of a compound of formulae (1), (1a) to (1i) or a compound selected from L1 to L34 and a compound of formulae (2) or (2a) to (2c) or a compound selected from B1 to B14.

The compositions according to the invention as described or preferably described above are suitable for use in organic electronic devices. An organic electronic device here means a device comprising at least one layer comprising at least one organic compound. However, the device may also comprise an inorganic material or a layer consisting entirely of an inorganic material.

The present invention therefore also relates to the use of a composition as described or preferably described above, in particular a mixture selected from M1 to M224, in an organic electronic device.

The components or ingredients of the composition may be processed by vapor deposition or from solution. If the composition is to be administered from a solution, the formulation of the composition according to the invention must comprise at least one further solvent. These formulations may be, for example, solutions, dispersions or emulsions. For this reason, a mixture of two or more solvents may be preferably used.

The invention therefore also relates to a formulation comprising a composition according to the invention and at least one solvent.

Suitable and preferred solvents are, for example, toluene, anisole, o-, m-or p-xylene, methyl benzoate, mesitylene, tetrahydronaphthalene, veratrole, THF, methyl-THF, THP, chlorobenzene, dioxane

Alkanes, phenoxytoluene (especially 3-phenoxytoluene), (-) -methanone, 1,2,3, 5-tetramethylbenzene, 1,2,4, 5-tetramethylbenzene, 1-methylnaphthalene, 2-methylbenzothiazole, 2-phenoxyethanol, 2-pyrrolidone, 3-methylanisole, 4-methylanisole, 3, 4-dimethylanisole, 3, 5-dimethylanisole, acetophenone, α -terpineol, benzothiazole, butyl benzoate, cumene, cyclohexanol, cyclohexanone, cyclohexylbenzene, decalin, dodecylbenzene, ethyl benzoate, indane, methyl benzoate, NMP, p-cymene, ethoxybenzene, 1, 4-diisopropylbenzene, dibenzyl ether, diethylene glycol butyl methyl ether, triethylene glycol butyl methyl ether, diethylene glycol dibutyl ether, triethylene glycol dimethyl ether, diethylene glycol monobutyl ether, tripropylene glycol dimethyl ether, tetraethylene glycol dimethyl ether, 2-isopropylnaphthalene, pentylbenzene, hexylbenzene, heptylbenzene, octylbenzene, 1, 1-bis (3, 4-dimethylphenyl) ethane or mixtures of these solvents.

The formulations can also comprise at least one further organic or inorganic compound, in particular a luminescent compound, in particular a phosphorescent emitter, and/or a further matrix material, which are also used in organic electronic devices. Suitable luminescent compounds and other host materials have already been mentioned above.

The invention also relates to the use of the composition according to the invention in an organic electronic device, preferably in an electron transporting and/or light emitting layer.

The organic electronic device is preferably selected from the group consisting of Organic Integrated Circuits (OIC), Organic Field Effect Transistors (OFET), Organic Thin Film Transistors (OTFT), organic electroluminescent devices, Organic Solar Cells (OSC), organic optical detectors and organic photoreceptors, with organic electroluminescent devices being particularly preferred.

Very particularly preferred organic electroluminescent devices using the compositions according to the invention are Organic Light Emitting Transistors (OLETs), Organic Field Quenching Devices (OFQDs), organic light emitting electrochemical cells (OLECs, LECs, LEECs), organic laser diodes (O-lasers) and Organic Light Emitting Diodes (OLEDs), particularly preferably OLECs and OLEDs, most preferably OLEDs.

The composition according to the present invention as described or preferably described above is preferably used in a layer having an electron transporting function in an electronic device. The layers are preferably Electron Injection Layers (EIL), Electron Transport Layers (ETL), Hole Blocking Layers (HBL) and/or light emitting layers (EML), particularly preferably ETL, EIL and/or EML. The compositions according to the invention are particularly preferably used in particular as matrix materials in EML.

The invention therefore also relates to an organic electronic device, in particular selected from one of the above electronic devices, and preferably comprising the inventive content as described or preferably described above in the following layers: the light-emitting layer (EML), the electron-transporting layer (ETL), the electron-injecting layer (EIL) and/or the hole-blocking layer (HBL) are very preferably in the EML, the EIL and/or the ETL and very particularly preferably in the EML.

In the case of the light-emitting layer, this is particularly preferably a phosphorescent layer, characterized in that, in addition to the composition as described or preferably described above, it also comprises phosphorescent emitters, in particular the emitters of table 5 or 6 or the preferred emitters as described above.

In a particularly preferred embodiment of the present invention, the electronic device is therefore an organic electroluminescent device, very particularly preferably an organic light-emitting diode (OLED), which comprises in the light-emitting layer (EML) the composition according to the invention as described or preferred above together with a phosphorescent emitter.

The composition according to the invention and the luminescent compound according to a preferred embodiment preferably comprise from 99.9 to 1% by volume, further preferably from 99 to 10% by volume, particularly preferably from 98 to 60% by volume, very particularly preferably from 97 to 80% by volume, based on the entire mixture comprising the luminophore and the matrix material, of a matrix material comprising at least one compound of the formula (1) and at least one compound of the formula (2) according to a preferred embodiment. Accordingly, the composition preferably comprises from 0.1 to 99% by volume, more preferably from 1 to 90% by volume, particularly preferably from 2 to 40% by volume, very particularly preferably from 3 to 20% by volume, of luminophore, based on the entire mixture comprising luminophore and matrix material. If the compounds are processed from solution, the corresponding amounts in% by weight are preferably used instead of the above-mentioned amounts in% by volume.

In addition to the cathode, the anode and the layer comprising the composition according to the invention, the electronic device may comprise further layers. These layers are selected, for example, from in each case one or more hole-injection layers, hole-transport layers, hole-blocking layers, light-emitting layers, electron-transport layers, electron-injection layers, electron-blocking layers, exciton-blocking layers, interlayers, charge-generation layers (IDMC 2003, taiwan; 21 st OLED conference (5), t.matsumoto, t.nakada, j.endo, k.mori, n.kawamura, a.yokoi, j.kido, multiphoton organic EL devices with charge-generation layers) and/or organic or inorganic p/n junctions. However, it should be noted that each of these layers need not be present.

The layer sequence in the organic electroluminescent device is preferably as follows:

anode/hole injection layer/hole transport layer/light emitting layer/electron transport layer/electron injection layer/cathode.

This layer order is the preferred order.

It should again be noted here that not all of the layers described are necessarily present, and/or that further layers may be present in addition.

According to the present invention, the organic electroluminescent device comprising the composition according to the present invention may comprise a plurality of light-emitting layers. In this case, the light-emitting layers particularly preferably have a plurality of emission peaks in total between 380nm and 750nm, so that white light is emitted overall, i.e. a plurality of light-emitting compounds which are capable of fluorescence or phosphorescence and emit blue or yellow or orange or red light are used in the light-emitting layer. Particularly preferred are three-layer systems, i.e. systems having three light-emitting layers, three of which exhibit blue, green and orange or red light emission (see, for example, WO 2005/011013 for basic structures). It should be noted that, in order to produce white light, it may also be appropriate to use one kind of emitter compound emitting light over a wide wavelength range alone instead of a plurality of emitter compounds emitting colored light.

Suitable charge transport materials which can be used in the hole injection layer or hole transport layer or electron blocking layer or electron transport layer of the organic electroluminescent device according to the invention are, for example, the compounds disclosed in y.shirota et al, chem.rev.2007, 107(4), 953-1010 or other materials used in these layers according to the prior art.

Materials which can be used for the electron transport layer are all materials which are used as electron transport materials in electron transport layers according to the prior art. Particularly suitable are aluminum complexes (e.g. Alq)₃) Zirconium complexes (e.g. Zrq)₄) Benzimidazole derivatives, triazine derivatives, pyrimidine derivatives, pyridine derivatives, pyrazine derivatives, quinoxaline derivatives, quinoline derivatives, and triazine derivatives,Oxadiazole derivatives, aromatic ketones, lactams, boranes, phosphorus diazacyclo-slow derivatives and phosphine oxide derivatives. Other suitable materials are derivatives of the above-mentioned compounds disclosed in JP2000/053957, WO 2003/060956, WO 2004/028217, WO 2004/080975 and WO 2010/072300.

Preferred hole-transporting materials are in particular materials which can be used in hole-transporting, hole-injecting or electron-blocking layers, for example indenofluorenamine derivatives (e.g. according to WO 06/122630 or WO 06/100896), amine derivatives as disclosed in EP 1661888, hexaazaterphenyl derivatives (e.g. according to WO 01/049806), amine derivatives containing fused aromatic rings (e.g. according to US 5,061,569), amine derivatives as disclosed in WO 95/09147, monobenzoindenofluorenamines (e.g. according to WO08/006449), dibenzoindenofluorenamines (e.g. according to WO 07/140847), spirobifluorinamines (e.g. according to WO 2012/034627 or EP 12000929.5 not yet disclosed), fluorenamines (e.g. according to WO 2014/015937, WO 2014/015938 and WO 2014/015935), spirodibenzopyranamines (e.g. according to WO 2013/083216) and acridine derivatives (e.g. according to WO 2012/150001).

The cathode of the electronic device preferably comprises a metal having a low work function, a metal alloy comprising a plurality of metals such as alkaline earth metals, alkali metals, main group metals or lanthanides (e.g. Ca, Ba, Mg, Al, In, Mg, Yb, Sm, etc.) or a multilayer structure. Also suitable are alloys comprising an alkali or alkaline earth metal and silver, for example alloys comprising magnesium and silver. In the case of a multilayer structure, in addition to the metals mentioned, it is also possible to use other metals having a higher work function, for example Ag or Al, in which case metal combinations, for example Ca/Ag, Mg/Ag or Ba/Ag, are generally used. It is also preferred to introduce a thin intermediate layer of a material having a high dielectric constant between the metal cathode and the organic semiconductor. Suitable for this purpose are, for example, alkali metal fluorides or alkaline earth metal fluorides, and also the corresponding oxides or carbonates (e.g. LiF, Li)₂O、BaF₂、MgO、NaF、CsF、Cs₂CO₃Etc.). Furthermore, lithium quinolate (LiQ) can be used for this purpose. The layer thickness of this layer is preferably between 0.5 and 5 nm.

The anode preferably comprises a material having a high work function. The anode preferably has a work function greater than 4.5eV relative to vacuum. On the one hand, metals with a high redox potential, such as Ag, Pt or Au, are suitable for this purpose. On the other hand, metal/metal oxide electrodes (e.g., Al/Ni/NiOx, Al/PtOx) may also be preferred. For certain applications, at least one of the electrodes must be transparent or partially transparent in order to facilitate irradiation of the organic material (organic solar cells) or coupling-out of light (OLEDs, O-lasers). Preferred anode materials herein are conductive mixed metal oxides. Indium Tin Oxide (ITO) or Indium Zinc Oxide (IZO) is particularly preferable. Also preferred are conductively doped organic materials, especially conductively doped polymers. Furthermore, the anode may also consist of multiple layers, for example an inner layer of ITO and an outer layer of a metal oxide, preferably tungsten oxide, molybdenum oxide or vanadium oxide.

During production, the organic electronic device is thus suitably (depending on the application) structured, provided with contact points and finally sealed, since the lifetime of the device according to the invention in the presence of water and/or air is shortened.

In another preferred embodiment, the organic electronic device comprising the composition according to the invention is characterized in that the one or more organic layers comprising the composition according to the invention are applied by a sublimation process, wherein the thickness in the vacuum sublimation unit is less than 10^-5Mbar, preferably less than 10^-6The material is applied by vapour deposition at an initial pressure of mbar. However, the initial pressure here may also be even lower, for example less than 10^-7Millibar.

Preference is likewise given to organic electroluminescent devices which are characterized in that one or more layers are applied by means of the OVPD (organic vapor deposition) method or by means of carrier gas sublimation, where 10 is the value^-5The material is applied at a pressure between mbar and 1 bar. One special case of such a method is the OVJP (organic vapor jet printing) method, in which the material is applied directly through a nozzle and is thus structured (for example MS Arnold et al, appl. phys. lett.2008, 92, 053301).

Furthermore, preference is given to organic electroluminescent devices which are characterized in that one or more layers are produced from solution, for example by spin coating, or by any desired printing method, for example screen printing, flexographic printing, nozzle printing or offset printing, but particularly preferably LITI (photo induced thermal imaging, thermal transfer printing) or inkjet printing. For this purpose, soluble compounds of the components of the composition according to the invention are necessary. High solubility can be achieved by appropriate substitution of the corresponding compounds. The advantage of processing from solution is that the layer comprising the composition according to the invention can be applied very simply and inexpensively. This technique is particularly suitable for mass production of organic electronic devices.

Hybrid methods are also possible, in which one or more layers are applied, for example from solution, and one or more other layers are applied by vapor deposition.

These methods are generally known to those skilled in the art and can be applied to organic electroluminescent devices.

The invention therefore also relates to a method for producing an organic electronic component comprising a composition according to the invention as described above or preferably described, characterized in that at least one organic layer comprising a composition according to the invention is applied by vapor deposition, in particular by a sublimation process and/or by an OVPD (organic vapor deposition) process, and/or by sublimation with a carrier gas, or from a solution, in particular by spin coating or by a printing process.

In the case of the manufacture of organic electronic devices by vapor deposition, there are basically two possibilities as to how to apply or vapor deposit onto any desired substrate an organic layer which is intended to comprise a composition according to the invention and which may comprise a plurality of different constituents. In one aspect, the materials used may each be present in one material source and eventually evaporated from multiple material sources ("co-evaporation"). Alternatively, multiple materials may be premixed, and the mixture may be contained in a single material source and then ultimately vaporized from the material source ("premixed vaporization"). This enables the vapour deposition of layers with uniformly distributed components to be achieved in a simple and fast manner without the need for precise control of a plurality of material sources.

The invention therefore also relates to a process which is characterized in that at least one compound of the formula (1) as described or preferred above and at least one compound of the formula (2) as described or preferred above, optionally together with further materials as described or preferred above, are deposited from the gas phase, either sequentially or simultaneously, from at least two material sources, and an organic layer is formed.

In a preferred embodiment of the invention, the at least one organic layer is applied by vapor deposition, wherein the ingredients of the composition are premixed and evaporated from a single material source.

The invention therefore also relates to a process which is characterized in that a composition according to the invention as described above or preferably described is used as a source of material for vapor deposition, optionally together with other materials, and forms an organic layer.

Furthermore, the present invention relates to a method for producing an organic electronic component comprising a composition according to the invention as described above or preferably described, characterized in that a formulation according to the invention as described above is used for applying an organic layer.

The composition according to the invention or the device according to the invention is characterized by the following surprising advantages compared to the prior art:

the use of the compositions according to the invention in organic electronic devices, in particular in organic electroluminescent devices, in particular in OLEDs or OLECs, leads to a significant increase in the lifetime of the devices.

As can be seen from example 1 shown below, the use of two electron transporting hosts (e.g. lactam derivatives and triazine-carbazole derivatives) with a green emitter concentration of 10% in the EML can result in good voltage and moderate efficiency. However, the lifetime of the assembly is very short (V1 and V2). It is known to the person skilled in the art that the lifetime of an OLED generally decreases with decreasing concentration of the emitter.

By a specific combination of the compound of formula (1) represented by compound L2 with the compound of formula (2) represented by compound B14(BisCbz1) (see example E1 of the present invention), or with compound B3(BisCbz2) (in example E3 of the present invention), an excellent improvement in lifetime is achieved at a luminophore concentration of green luminophores of 12% in EML, with the same module efficiency and module voltage. Even at the lower luminophore concentrations of only 7% in the EML (examples E2 and E4), the lifetime is still significantly improved compared to the prior art.

An improvement of more than 4 times the lifetime at comparable module voltages and comparable or improved module efficiencies can preferably be achieved by a combination of a compound of formula (1) according to the invention as described above, wherein n is 1 and Z has the meaning specified above or preferably specified, with a compound of formula (2) as described above, wherein the emitter concentration in the light-emitting layer is from 2 to 15% by weight.

In example E1, this advantage is demonstrated by representative compounds of the formula (1) at a luminophore concentration of 12% by using compound L2 with biscarbazole B14 (abbreviated BisCbz 1).

Even with a lower emitter concentration of only 7% in the EML (the lifetime of the OLED is usually reduced), the lifetime achieved by the combination according to the invention is still significantly improved compared to the prior art. In example E2, this is demonstrated by representative compounds of the formula (1) at a luminophore concentration of 7% using compound L2 and biscarbazole B14 (abbreviated BisCbz 1).

Comparative examples V1 and V2 differ in that the substituent Ar in the biscarbazole of formula (2)₁Or Ar₂Or a substituent R¹With an extremely electron-rich heteroaromatic ring system having 6 aromatic ring atoms and 3 nitrogen atoms. The person skilled in the art cannot foresee that the lower electron density of the biscarbazole of formula (2) selected according to the invention leads to improved vapor deposition properties and thus to an improvement of the lifetime of the electronic device, in particular of the OLED, of more than a factor of 4.

Compared to the lactam and biscarbazole-containing composition of WO2013/064206,

the composition has a higher thermal stability and is less sensitive to crystallization.

The compositions according to the invention are very suitable for use in light-emitting layers and show improved performance data, in particular in terms of lifetime, compared with the compounds from the prior art as described above.

The composition according to the invention can be easily processed and is therefore very suitable for mass production for commercial use.

The compositions of the invention can be premixed and vapor deposited from a single material source, so that organic layers having a uniform distribution of the components used can be produced in a simple and rapid manner.

These above-mentioned advantages are not accompanied by a deterioration of other electronic properties of the electronic device.

It should be noted that variations of the embodiments described in the present invention fall within the scope of the invention. Each feature disclosed in this specification may be replaced by an alternative feature serving the same, equivalent, or similar purpose, unless expressly excluded. Thus, unless expressly stated otherwise, each feature disclosed in this specification is to be considered as an example of a generic series of features or as equivalent or similar features.

All features of the invention may be combined with each other in any manner, unless some features and/or steps are mutually exclusive. This applies in particular to the preferred features of the invention. Also, features that are not necessarily combined may be used separately (rather than in combination).

The teachings related to the technical actions disclosed in the present invention can be extracted and combined with other embodiments.

The invention is explained in more detail by the following examples, without wishing to restrict the invention thereby.

The general method comprises the following steps:

determination of orbital energy and electronic states

For this purpose, we use "Gaussian 09, revision d.01" software package (Gaussian company) in the present application for the calculation of metal-free organic substances (denoted by the "org." method), first of all the semi-empirical method AM1(Gaussian input line "# AM1 opt") is used for geometric optimization with a charge of 0 and a multiplicity of 1, then the energy calculations (single points) are carried out on the electron ground and triplet energy levels according to the optimized geometry, here TDDFT (time-varying density functional theory) method B3PW91 ") and 6-31g (d) basis set (Gaussian input line" # B3 91/6-31g (d) td (50-50, wattles 4) ") (charge # 0, multiplicity 1) are used for organometallic compounds (denoted by" org-m "method) and the energy calculation (assumed by" bold type p-x-t-31 g "(r) is used for geometric calculation with a charge of # 0, multiplicity of 1) and the energy calculation (assumed intrinsic energy calculation (r-x-t) set (r-x-t:

HOMO(eV)＝(HEh*27.212)*0.8308-1.118；

LUMO(eV)＝(LEh*27.212)*1.0658-0.5049。

the triplet state T1 of the material is defined as the relative excitation energy (in eV) of the triplet state with the lowest energy calculated from quantum chemical energy.

The singlet state energy level S1 is defined as the relative excitation energy (in eV) of the singlet state with the second lowest energy calculated from quantum chemical energy.

The lowest energy singlet state is referred to as S0.

The methods described herein are independent of the software package used and give the same results throughout. Examples of programs often used for this purpose are "Gaussian 09" (Gaussian) and Q-Chem 4.1 (Q-Chem). In this application, the "Gaussian 09, revision D.01" software package is used to calculate energy.

Example 1: fabrication of OLEDs

The use of the material combinations according to the invention in OLEDs is given in the following examples E1, E2, E3 and E4 (see table 7).

129页详细技术资料下载

上一篇：一种医用注射器针头装配设备

下一篇：发光陶瓷和波长转换装置

Composition for organic electronic device

相关技术

网友询问留言