EP2206175A1

EP2206175A1 - Use of diphenylamino-bis(phenoxy)- and bis(diphenylamino)-phenoxytriazine compounds

Info

Publication number: EP2206175A1
Application number: EP08842691A
Authority: EP
Inventors: Evelyn Fuchs; Nicolle Langer; Christian Lennartz; Peter Strohriegl; Michael Rothmann
Original assignee: BASF SE
Current assignee: BASF SE
Priority date: 2007-10-24
Filing date: 2008-10-21
Publication date: 2010-07-14
Also published as: JP2011502189A; KR20100092451A; WO2009053346A1; CN101884122B; US20100258790A1; CN101884122A

Abstract

The present invention relates to an organic light-emitting diode comprising at least one diphenylamino-bis(phenoxy)- or at least one bis(diphenylamino)- phenoxytriazine compound, a light-emitting layer comprising at least one diphenylamino-bis(phenoxy)- or at least one bis(diphenylamino)-phenoxytriazine compound, to the use of the above-mentioned compounds as matrix material, hole/exciton blocker material, electron/exciton blocker material, hole injection material, electron injection material, hole conductor material, and/or electron conductor material, and to a device selected from the group consisting of stationary display screens, mobile display screens, and lighting units containing at least one organic light-emitting diode according to the invention.

Description

Use of diphenylamino bis (phenoxy) and bis (diphenylamino) phenoxytriazine compounds

description

The present invention relates to an organic light-emitting diode containing at least one diphenylamino-bis (phenoxy) - or at least one bis (diphenylamino) - phenoxytriazine compound, a light-emitting layer containing at least one diphenylamino-bis (phenoxy) - or at least one bis (diphenylamino) - phenoxotriazine compound, the use of the abovementioned compounds as matrix material, hole / exciton blocker material, electron / exciton blocker material, hole injection material, electron injection material, hole conductor material and / or electron conductor material and a device selected from the group consisting of stationary screens, Mobile screens and lighting units contain at least one organic light-emitting diode according to the invention.

In organic light emitting diodes (OLEDs), the property of materials is used to emit light when excited by electric current. OLEDs are of particular interest as an alternative to cathode ray tubes and to liquid crystal displays for the production of flat panel displays. Due to the very compact design and the intrinsically low power consumption, devices containing OLEDs are particularly suitable for mobile applications, for example for applications in mobile phones, laptops, etc., as well as for lighting.

The basic principles of the functioning of OLEDs and suitable structures (layers) of OLEDs are known to the person skilled in the art and are mentioned, for example, in WO 2005/113704 and the literature cited therein. As light-emitting materials (emitters), phosphorescent materials (phosphorescence emitters) can be used in addition to fluorescent materials (fluorescence emitters). The phosphorescence emitters are usually organometallic complexes which, in contrast to the fluorescence emitters which exhibit singlet emission, exhibit triplet emission (triplet emitters) (MA Baldow et al., Appl. Phys. Lett. 1999, 75, 4 to 6). For quantum mechanical reasons, when using the triplet emitter (phosphorescence emitter) up to fourfold quantum, energy and power efficiency is possible. In order to put into practice the advantages of using the organometallic triplet emitters (phosphorescent emitters), it is necessary to provide device compositions which have a long operating life, good efficiency, high stability against thermal stress, and low use and low energy consumption Operating voltage have. Such device compositions may contain, for example, special matrix materials in which the actual light emitter is present in distributed form. Furthermore, the compositions may contain blocker materials, wherein hole, excitation and / or electron blockers may be present in the device compositions. Alternatively or alternatively, the device compositions may further comprise hole injection materials and / or electron injection materials and / or hole conductor materials and / or electron conductor materials. The selection of the above-mentioned materials, which are used in combination with the actual light emitter, has a significant influence, inter alia, on the efficiency and the lifetime of the OLEDs.

Many different materials for use in OLEDs are proposed in the prior art. Among the suggested materials are also those which have diphenylamino-bis (phenoxy) - or bis (diphenylamino) phenoxytriazine compound.

JP-A 2002-193952 relates to amino-substituted triazine derivatives which are useful as light-emitting materials. According to JP-A 2002-193952, the compounds exhibit blue fluorescence with high intensity and are suitable for use in light-emitting elements. The amino group is linked in the compounds according to JP-A 2002-193952 via a linker with the triazine skeleton. Furthermore, the triazine skeleton may have other non-amino substituents. Diphenylamino-bis (phenoxy) - or bis (diphenylamino) -phenoxytriazine compounds are not mentioned in JP-A 2002-193952.

US Pat. No. 5,716,722 discloses OLEDs which, as hole transport material, have a compound with a triazine ring with at least one directly bound diphenylamino group. According to US 5,716,722 hole transport materials are to be provided, which are difficult to crystallize, since the crystallization in the hole transport layer can lead to short circuits, so that no light emission takes place in the crystallized areas. Diphenylamino-bis (phenoxy) - or bis (diphenylamino) - phenoxytriazine compounds are not mentioned in US 5,716,722.

US 2006/0051616 A1 relates to organic compounds which simultaneously fluoresce and phosphoresce. The organic compounds may be triazine derivatives. The specification in US 2006/0051616 A1 discloses carbazolyl-substituted triazine derivatives which, in addition to two carbazolyl substituents, may carry a halogen-substituted phenoxy radical. According to US 2006/0051616 A1, the organic compounds can be used as emitter materials in organic light-emitting diodes. Other uses of the method described in US 2006/0051616 A1 th organic compounds, for example as a matrix material, blocking material or injection material are not mentioned in US 2006/0051616 A1.

The object of the present invention is to provide materials which are suitable for use in OLEDs, in particular for use as matrix material, in particular as matrix material in the light-emitting layer, hole / exciton blocker material, electron / exciton blocker material, hole injection material, Electron injection material, hole conductor material and / or Elektronenleiterma- material which have improved amorphous properties compared to the materials mentioned in the prior art, that is, have a reduced tendency to crystallize, as well as the provision of OLEDs with an improved property profile, resulting in improved performance , eg a prolonged life, good luminance, high quantum yields, etc., shows.

This object is achieved by an organic light-emitting diode containing at least one diphenylamino-bis (phenoxy) and / or bis (diphenylamino) -phenoxytriazine derivative of the general formula (I)

in which mean:

CR, N or P, or - if n = 0 - additionally O or S;

D is CR, N or P or, if n = 0, additionally O or S;

E is CR, N or P or, if n = 0, additionally O or S;

G is CR ¹⁴ , N or P or, if n = 0, additionally O or S; L is CR ¹⁵ , N or P, or - if n = 0 - additionally O or S; Dr \ ^8, Dr \ ^9, Dr \ ¹⁰ are independently hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O- aryl, O-heteroaryl, SH, S-alkyl, S-aryl, halogen, pseudo-halogen, amino or further substituents with donor or acceptor action;

R ¹¹ , R ¹² , R ¹³ , R ¹⁴ , R ¹⁵ independently of one another are hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, pseudohalogen, Amino, further substituents with donor or acceptor action or a radical of the formula (i), (ii) or (iii)

wherein the radicals and groups X ', R ^1' , R ^{2 '} , R ^3' , R ^{4 '} , R ^5' , R ^{6 '} , R ^7' , R ^{8 '} , R ^9' and R ^{10 '} in the rest of formula (i), which radicals and groups X ^'a, R ^{1 a,} R ^{2 a,} R ^{3 a,} R ^{4' a,} R ^{5 a,} R ^{6 a,} R ^{7 a,} R ^{8 a,} R ^{9 a} and R ^{10 is O} in the radical of formula (ii) and the radicals and groups X ' ^b , R ^rb , R ^2'b , R ^3'b , R ^4'b , R ^5'b , R ^6'b , R ^7'b , R ^8'b , R ^{9 b} and R ^{10 b} in the radical of the formula (iii) independently of one another with regard to the radicals and groups X, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ and R ^{10 have} mentioned meanings, and

the radicals R ³⁴ , R ³⁵ , R ³⁶ , R ³⁷ , R ³⁸ , R ³⁹ , R ⁴⁰ , R ^{34 '} , R ^35' , R ^{36 '} , R ³⁷ and R ^{38' are} independently hydrogen, alkyl, aryl, Heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, halogen, pseudohalogen, amino or other substituents with donor or acceptor action;

X

m

M is CR ²⁶ , N or P or, if m = 0, additionally O or S; R is CR ²⁷ , N or P or, if m = 0, additionally O or S; T is CR, N or P or, if m = 0, additionally O or S;

U is CR, N or P or, if m = 0, additionally O or S;

V is CR, N or P or, if m = 0, additionally O or S;

_D 16 D "I8 _D 19 _D 21 _D 23 _D 24 _D 25 are independently hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O- aryl, O-heteroaryl, SH, S-alkyl, S-aryl, Halogen, pseudohalogen, amino or other donor or acceptor substituents; independently of one another are hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, pseudohalogen, amino, others

Substituents with donor or acceptor effect; or a radical of the formulas (iv), (v) or (vi)

(Iv)

wherein the radicals and groups X ", R ¹ , Fr, FT, R ⁴ , R ^ö , R ^b , R ', R ^ö , R ^a and R j10" in the radical of formula (iv), the radicals and groups X " ^a , R ^{1" a} , R ^{2 "a} , R ^{3" a} , R ^{4 "a} , R ^{5" a} , R ^{6 "a} , R ^{7" a} , R ^{8 "a} , R ^{9" a} and R ^{10 "a} in the radical of formula (v) and the radicals and groups X" ^b , R ^{1 "b} , R ^{2" b} , R ^{3 "b} , R ^{4" b} , R ^{5 "b} , R ^{6" b} , R ^{7 "b} , R ^8b , R ^{9" b} and R ^{10 "b} in the radical of the formula (vi) independently of one another denote the radicals and groups X, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ and R ^{10 have} mentioned meanings, and

the radicals R ^{34 "} , R ^35" , R ^{36 "} , R ^37" , R ^{38 "} , R ^{39 '} R ^40' R ^34"' R ^{35 "'} R ^36"' R ^{37 "} and R ^38" are each independently Hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, halogen, pseudohalogen, amino or other substituents with donor or acceptor action; n, m are independently 0 or 1, preferably 1. The expression "further substituents with donor or acceptor action" is understood to mean the abovementioned substituents with donor or acceptor action which are not expressly mentioned in the definition of the radicals R ¹ to R ³⁰ .

The present invention thus relates to specifically substituted tris (diphenylamino) triazine compounds having at least one aryloxy group. It has been found that these compounds are distinguished by a particularly low crystallization tendency and are particularly suitable for use in OLEDs.

Depending on their substitution pattern, the compounds of the formula (I) can be used either as a matrix, in particular as a matrix in the light-emitting layer, as a hole / exciton blocker, as electron / exciton blocker, as hole injection materials, as electron injection materials, as Hole conductor and / or used as an electron conductor. Corresponding layers of OLEDs are known to the person skilled in the art and are mentioned, for example, in WO 2005/113704 or WO 2005/019373.

Alkyl is to be understood as meaning substituted or unsubstituted C ₁ -C 20 -alkyl radicals. Preference is given to C 1 to C 10 -alkyl radicals, particularly preferably C 1 to C 6 -alkyl radicals. The alkyl radicals can be both straight-chain and branched. Furthermore, the alkyl radicals may be substituted with one or more substituents selected from the group consisting of CrC ₂ o-alkoxy, halogen, preferably F, and C ₆ -C ₃ o-aryl, which in turn may be substituted or unsubstituted substituted. Suitable aryl substituents as well as suitable alkoxy and halogen substituents are mentioned below. Examples of suitable alkyl groups are methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl and octyl, as well as C ₆ -C ₃ o-aryl, Ci-C _2O -AIkOXy- and / or halogen, especially F, substituted derivatives of the mentioned alkyl groups, for example CF ₃ . Both the n-isomers of the radicals mentioned and branched isomers such as isopropyl, isobutyl, isopentyl, sec-butyl, tert-butyl, neopentyl, 3,3-dimethylbutyl, 3-ethylhexyl, etc. are included. Preferred alkyl groups are methyl, ethyl, tert-butyl and CF ₃ .

By cycloalkyl are meant substituted or unsubstituted C ₃ -C ₂ O-AI ky I radicals. Preference is given to C ₃ - to Cio-alkyl radicals, more preferably C ₃ - to C ₈ -alkyl radicals. The cycloalkyl radicals may carry one or more of the substituents mentioned with respect to the alkyl radicals. Examples of suitable cyclic alkyl groups (cycloalkyl radicals) which may likewise be unsubstituted or substituted by the radicals mentioned above with respect to the alkyl groups are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl and cyclodecyl. If appropriate, these may also be polycyclic ring systems, such as decalinyl, norbornyl, bornanyl or adamantyl. Suitable O-alkyl and S-alkyl groups are Ci-C ₂ o-alkoxy and C ₁ -C ₂₀ - alkylthio, and derive respectively from the above-mentioned C ₁ -C ₂₀ - alkyl radicals from. For example, OCH ₃ , OC ₂ H ₅ , OC ₃ H ₇ , OC ₄ H ₉ and OC ₈ H ₁₇ and SCH ₃ , SC ₂ H ₅ , SC ₃ H ₇ , SC ₄ H ₉ and SC ₈ H _{17 may be mentioned here} , C ₃ H ₇ , C ₄ H ₉ and C ₈ H ₁₇ include both the n-isomers and branched isomers such as isopropyl, isobutyl, sec-butyl, tert-butyl and 2-ethylhexyl. Particularly preferred alkoxy or alkylthio groups are methoxy, ethoxy, n-octyloxy, 2-ethylhexyloxy and SCH ₃ .

Suitable halogen radicals or halogen substituents for the purposes of the present application are fluorine, chlorine, bromine and iodine, preferably fluorine, chlorine and bromine, particularly preferably fluorine and chlorine, very particularly preferably fluorine.

Suitable pseudohalogen radicals in the context of the present application are CN, SCN, OCN, N ₃ and SeCN, CN and SCN being preferred. Most preferred is CN.

Suitable aryl radicals are C ₆ -C ₃₀ -aryl radicals which are derived from monocyclic, bicyclic or tricyclic aromatics which contain no ring heteroatoms. Unless they are monocyclic systems, the term aryl for the second ring also means the saturated form (perhydroform) or the partially unsaturated form (for example the dihydroform or tetrahyroform), provided the respective forms are known and stable. That is, in the present invention, the term aryl includes, for example, bicyclic or tricyclic radicals in which both both and all three radicals are aromatic, as well as bicyclic or tricyclic radicals in which only one ring is aromatic, and tricyclic radicals wherein two rings are aromatic. Examples of aryl are: phenyl, naphthyl, indanyl, 1, 2-dihydronaphthenyl, 1, 4-dihydronaphthenyl, indenyl, anthracenyl, phenanthrenyl or 1, 2,3,4-tetrahydronaphthyl. Particularly preferred are C ₆ -C ₁₀ -aryl radicals, for example phenyl or naphthyl, very particularly preferably C ₆ -aryl radicals, for example phenyl.

The aryl radicals may be unsubstituted or substituted by one or more further radicals. Suitable further radicals are selected from the group consisting of C ₁ -C ₂₀ -alkyl, C ₆ -C ₃₀ -aryl or substituents with donor or acceptor action, suitable substituents with donor or acceptor action being mentioned below. The C ₆ -C ₃ are preferably unsubstituted o-aryl or substituted with one or more C ₂₀ alkoxy groups, CN, CF _3, F or amino groups. Further preferred substitutions of the C ₆ -C ₃₀ aryl radicals are dependent on the intended use of the compounds of the general formula (I) and are mentioned below. Suitable O-aryl and S-aryl groups are C ₆ -C ₃₀ aryloxy, C ₆ -C ₃ o-alkylthio groups and are derived respectively from the aforementioned C ₆ -C ₃₀ aryl residues from. Particularly preferred are phenoxy and phenylthio.

Heteroaryl is to be understood as meaning unsubstituted or substituted heteroaryl radicals having 5 to 30 ring atoms, which may be monocyclic, bicyclic or tricyclic, some of which can be derived from the abovementioned aryl, in which at least one carbon atom in the aryl skeleton is replaced by a heteroatom , Preferred heteroatoms are N, O and S. Particularly preferably, the heteroaryl radicals have 5 to 13 ring atoms. Especially preferred is the backbone of the heteroaryl radicals selected from systems such as pyridine and five-membered heteroaromatics such as thiophene, pyrrole, imidazole or furan. These backbones may optionally be fused with one or two six-membered aromatic radicals. Suitable anellated heteroaromatics are carbazolyl, benzimidazolyl, benzofuryl, dibenzofuryl or dibenzothiophenyl. The backbone may be substituted at one, several or all substitutable positions, suitable substituents being the same as those already mentioned under the definition of C ₆ -C ₃₀ -aryl. Preferably, however, the heteroaryl radicals are unsubstituted. Suitable heteroaryl radicals are, for example, pyridin-2-yl, pyridin-3-yl, pyridin-4-yl, thiophen-2-yl, thiophen-3-yl, pyrrol-2-yl, pyrrol-3-yl, furan-2 - yl, furan-3-yl and imidazol-2-yl and the corresponding benzanellierten radicals, in particular carbazolyl, benzimidazolyl, benzofuryl, dibenzofuryl or dibenzothiophenyl.

Amino groups are radicals of the general formula -NR ³¹ R ³² , suitable radicals R ³¹ and R ^{32 being mentioned} below. Examples of suitable amino groups are diarylamino groups such as diphenylamino and dialkylamino groups such as dimethylamino, diethylamino and arylalkylamino groups such as phenylmethylamino.

For the purposes of the present application, groups / substituents with donor or acceptor action are understood to mean the following groups:

C ₁ -C ₂₀ -alkoxy, C ₆ -C ₃₀ -aryloxy, C ₁ -C ₂₀ -alkylthio, C ₆ -C ₃₀ -arylthio, SiR ³¹ R ³² R ³³ , halogen radicals, halogenated C ₁ -C ₂₀ -alkyl radicals, carbonyl (- CO (R ³¹ )), carbonylthio (- C = O (SR ³¹ )), carbonyloxy (- C = O (OR ³¹ )), oxycarbonyl (- OC = O (R ³¹ )), thiocarbonyl (- SC = 0 ( R ³¹ )), amino (-NR ³¹ R ³² ), OH, pseudohalogeno radicals, amido (- C = O (NR ³¹ )), - NR ³¹ C = O (R ³² ), phosphonate (- P (O) (OR ³¹ ) ₂ , phosphate (-OP (O) (OR ³¹ ) ₂ ), phosphine (- PR ³¹ R ³² ), phosphine oxide (-P (O) R ³¹ ₂ ), sulfate (-OS (O) ₂ OR ³¹ ) , Sulfoxide (-S (O) R ³¹ ), sulfonate (-S (O) ₂ OR ³¹ ), sulfonyl (-S (O) ₂ R ³¹ ), sulfonamide (-S (O) ₂ NR ³¹ R ³² ), NO ₂ , boronic acid esters (-OB (OR ³¹ ) ₂ ), imino (-C = NR ³¹ R ³² ), borane radicals, stannane radicals, hydrazine radicals, hydrazone radicals, oxime radicals, nitroso groups, diazo groups, vinyl groups, (= Sulfonate) and boronic acid groups, sulfoximines, alanes, germanes, boroximes and borazines.

Preferred substituents with donor or acceptor action are selected from the group consisting of:

C ₁ to C ₂ o-alkoxy, preferably C ₁ -C 6 -alkoxy, particularly preferably ethoxy or methoxy; C6-C ₃ o-aryloxy, preferably C ₆ -Cio-aryloxy, most preferably phenyloxy; SiR ³¹ R ³² R ³³ , wherein R ³¹ , R ³² and R ^{33 are} preferably each independently substituted or unsubstituted alkyl or substituted or unsubstituted phenyl; at least one of the radicals R ³¹ , R ³² or R ³³ is particularly preferably substituted or unsubstituted phenyl, very particularly preferably at least one of the radicals R ³¹ , R ³² and R ^{33 is} substituted phenyl, suitable substituents being mentioned above; Halogen radicals, preferably F, Cl, Br, particularly preferably F or Cl, very particularly preferably F, halogenated dC ₂ o-alkyl radicals, preferably halogenated C ₁ -C ₆ -alkyl radicals, very particularly preferably fluorinated C ₁ -C ₆ -alkyl radicals, eg. CF ₃ , CH ₂ F, CHF ₂ or C ₂ F ₅ ; Amino, preferably dimethylamino, diethylamino or diphenylamino; OH, pseudohalogen radicals, preferably CN, SCN or OCN, more preferably CN, -C (O) OC _r C ₄ alkyl, preferably -C (O) OMe, P (O) R ₂ , preferably P (O) Ph ₂ or SO ₂ R ₂ , preferably SO ₂ Ph.

Very particularly preferred substituents having donor or acceptor selected from the group consisting of methoxy, phenyloxy, halogenated CrC ₄ - alkyl, preferably CF _3, CH ₂ F, CHF _2, C ₂ F _5, halogen, preferably F, CN, SiR ³¹ R ³² R ³³ , where suitable radicals R ³¹ , R ³² and R ^{33 are} already mentioned, diphenylamino, -C (O) -O-C ₄ -alkyl, preferably -C (O) OMe, P (O) Ph ₂ , SO ₂ Ph.

By the abovementioned groups with donor or acceptor action, it should not be ruled out that further of the abovementioned radicals and groups may also have a donor or acceptor action. For example, the above-mentioned heteroaryl radicals are also donor or acceptor groups and the dC ₂ o-alkyl radicals are donor-donating groups.

The radicals R ³¹ , R ³² and R ³³ mentioned in the abovementioned groups with donor or acceptor action have the meanings already mentioned above, ie R ³¹ , R ³² , R ³³ independently of one another:

Substituted or unsubstituted Ci-C ₂₀ alkyl or substituted or unsubstituted C6-C ₃ o-aryl, where suitable and preferred alkyl and aryl radicals are above overall Nannt. Particularly preferably, the radicals R ³¹ , R ³² and R ^{33 are} C 1 -C ₆ -alkyl, z. For example, methyl, ethyl or i-propyl, phenyl. In a preferred embodiment - in the case Ie of SiR ³¹ R ³² R ³³ - R ³¹ , R ³² and R ^{33 are} preferably each independently substituted or unsubstituted C ₁ -C 20 -alkyl or substituted or unsubstituted phenyl; more preferably at least one of R ³¹ , R ³² or R ^{33 is} substituted or unsubstituted phenyl, most preferably at least one of R ³¹ , R ³² and R ^{33 is} substituted phenyl, suitable substituents being mentioned above.

The compounds of the formula (I) are preferably compounds which have 1 or 2 triazine groups, ie the compounds of the formula (I) preferably have one or no radical selected from the formulas (i), (ii) , (iii), (iv), (v) and (vi).

In a preferred embodiment, the present invention relates to compounds of the formula (I) in which at least one of the radicals R ¹ to R ^{30 is} not hydrogen. Preference is given to compounds of the formula (I) in which at least one of the radicals R ² , R ³ , R ⁴ , R ⁷ , R ⁸ , R ⁹ , R ¹² , R ¹³ , R ¹⁴ , and / or at least one of the radicals R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²² , R ²³ , R ²⁴ or R ²⁷ , R ²⁸ , R ^{29 is} not hydrogen.

Particular preference is given to compounds of the formula (I) which have 1 to 10, preferably 1, 2, 3, 4, 5 or 6, radicals R ¹ to R ³⁰ which are not hydrogen. The radicals which are not hydrogen are preferably selected from the abovementioned radicals R ² , R ³ , R ⁴ , R ⁷ , R ⁸ , R ⁹ , R ¹² , R ¹³ , R ¹⁴ , R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²² , R ²³ , R ²⁴ , R ²⁷ , R ²⁸ and R ^{29 are} selected radicals. Particularly preferably, all other radicals R ¹ to R ^{30 are} hydrogen. Thus, compounds of formula (I) are particularly preferred wherein the o-positions of the phenyl radicals attached to the nitrogen atom or oxygen atom attached to the triazine skeleton carry hydrogen atoms. The p and m positions are independently substituted with the aforementioned radicals (which may also be hydrogen atoms). Another object of the present invention are therefore the organic light emitting diodes according to the invention, wherein the radicals R ¹ , R ⁵ , R ⁶ , R ¹⁰ , R ¹¹ , R ¹⁵ , R ¹⁶ , R ²⁰ , R ²¹ , R ²⁵ , R ²⁶ and R ^{30 is} hydrogen.

In the compounds of the formula (I), the groups A, D, E, G, L and M, R, T, U and V are preferably, independently of one another,

A is CR ¹¹ , N or P or, if n = 0, additionally O or S; preferably CR ¹¹ ;

D is CR ¹² , N or P or, if n = 0, additionally O or S; preferably CR ¹² ; E is CR ¹³ , N or P or, if n = 0, additionally O or S; preferably CR ¹³ ;

G is CR ¹⁴ , N or P or, if n = 0, additionally O or S; preferably CR ¹⁴ ;

L is CR ¹⁵ , N or P, or - if n = 0 - additionally O or S; preferably CR ¹⁵ ;

M is CR ²⁶ , N or P or, if m = 0, additionally O or S; preferably CR ²⁶ ;

R is CR ²⁷ , N or P or, if m = 0, additionally O or S; prefers

CR ²⁷ ;

T is CR ²⁸ , N or P or, if m = 0, additionally O or S; prefers

CR ²⁸ ;

U CR ²⁹ , N or P, or - if m = 0 - additionally O or S; preferably CR ²⁹ ;

V CR ³⁰ , N or P, or - if m = 0 - additionally O or S; preferably CR ³⁰ .

Preferably, 0, 1, 2 or 3 of the groups A, D, E, G, L or M, R, T, U and V denote nitrogen and the remaining groups mean one of the carbon-containing group mentioned above in the definitions.

The radicals R ¹¹ , R ¹² , R ¹³ , R ¹⁴ , R ^{15 are} independently hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl , Pseudohalogen, amino, another substituent with donor or acceptor action or a radical selected from the formulas (i), (ii) and (iii)

wherein the radicals and groups X ', R ^1' , R ^{2 '} , R ^3' , R ^{4 '} , R ^5' , R ^{6 '} , R ^7' , R ^{8 '} , R ^9' and R ^{10 '} in the rest of formula (i), which radicals and groups X ^'a, R ^{1 a,} R ^{2 a,} R ^{3 a,} R ^{4 a,} R ^{5 a,} R ^{6 a,} R ^{7 a,} R ^{8 a,} R ^{9 a} and R ^{1O A} in the radical of formula (ii) and the radicals and groups X ^'b, R ^rb, R ^2'b, ^3'b R, R ^4'b, R ^{5 b,} R ^{6 b,} R ^{7 b,} R ^{8 b} , R ^{9 b} and R ^{10 b} in the radical of the formula (iii) independently of one another with regard to the radicals and groups X, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ and R ^{10 have} the meanings mentioned, and the radicals R ³⁴ , R ³⁵ , R ³⁶ , R ³⁷ , R ³⁸ , R ³⁹ , R ⁴⁰ , R ^{34 '} , R ^35' , R ^{36 '} , R ³⁷ and R ³⁸ independently of one another denote hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, halogen, pseudo-halogen, amino or further substituents with donor or acceptor action;

preferably hydrogen, alkyl, O-alkyl, O-aryl, pseudohalogen or a radical selected from the formulas (i), (ii) and (iii); particularly preferably hydrogen, C ₁ - to C ₆ -alkyl, C 2 - to C ₆ -alkyl, OC ₆ -aryl or a radical selected from the formulas (i), (ii) and (iii); most preferably methyl, O-methyl or a radical selected from the formulas (i), (ii) and (iii). In a preferred embodiment, the compounds of formula (I) have one or no group selected from the formulas (i), (ii) and (iii), wherein - when a group selected from the formulas (i), (ii) and (iii) - one of the radicals R ¹² , R ¹³ or R ¹⁴ , preferably R ¹² or R ^{14 is} a radical selected from the formulas (i), (ii) and (iii).

Particularly preferred formulas (ii) and (iii) are the following formulas (iia) and (iiia):

wherein the radicals and groups have the meanings given above. Preferably, R ³⁹ and R ⁴⁰ and R ³⁷ independently of one another denote hydrogen, CH ₃ or CF ₃ and R ³⁴ and R ³⁶ independently of one another denote hydrogen or CH ₃ .

The radicals R ²⁶ , R ²⁷ , R ²⁸ , R ²⁹ , R ³⁰ independently of one another are hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl , Pseudohalogen, amino, another substituent with donor or acceptor action or a radical of the formulas (iv), (v) or (vi)

(Iv)

wherein the radicals and groups X ", R ¹ , R, FT, R ⁴ , R ^ö , R ^b , R ', R ^ö , R ^a and R ^ηu in the radical of the formula (iv), the radicals and groups X" ^a , R ^{1 "a} , R ^{2" a} , R ^{3 "a} , R ^{4" a} , R ^{5 "a} , R ^{6" a} , R ^{7 "a} , R ^{8" a} , R ^{9 "a} and R ^{10" a} in the radical of the formula (v) and the radicals and groups X " ^b , R ^{1" b} , R ^{2 "b} , R ^{3" b} , R ^{4 "b} , R ^{5" b} , R ^{6 "b} , R ^{7 "b} , R ^{8 b} , R ^{9" b} and R ^{10 "b} in the radical of the formula (vi) independently of one another with respect to the radicals and groups X, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ and R ^{10 have} mentioned meanings, and

the radicals R ^{34 "} , R ^35" , R ^{36 "} , R ^37" , R ^{38 "} , R ^{39 '} , R ^40' , R ^34" , R ^{35 "} , R ^36" , R ^{37 "} and R ^38" independently of one another hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, halogen, pseudohalogen, amino or other substituents with donor or acceptor action; preferably hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, pseudohalogen, amino or another substituent with donor or acceptor action; particularly preferably hydrogen, alkyl, O-alkyl, O-aryl or pseudohalogen; very particularly preferably hydrogen, d- to C ₆ alkyl, OC ₁ - to C ₆ - alkyl or O-Cβ-aryl; most preferably methyl, O-methyl.

The radicals R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ , R ¹⁰ and the radicals R ¹⁶ , R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²⁰ , R ²¹ , R ²² , R ²³ , R ²⁴ , R ²⁵ and the radicals R ³⁴ , R ³⁵ , R ³⁶ , R ³⁷ , R ³⁸ , R ³⁹ , R ⁴⁰ , R ^{34 '} , R ^35' , R ^{36 '} , R ³⁷ and R ^{38 '} and the radicals R ^{34 "} , R ^35" , R ^{36 "} , R ^37" , R ^{38 "} , R ^39' , R ^{40 '} , R ^34" , R ^{35 "} , R ^36" , R ^{37 "} and R ³⁸ independently represent hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, halogen, pseudohalogen, amino or another substituent with donor preferably hydrogen, alkyl, halogen-substituted alkyl, O-alkyl, O-aryl or pseudohalogen, particularly preferably hydrogen, C ₁ - to C ₆ -alkyl, substituted by one or more F atoms d- to C substituted _6- alkyl, C 2 - to C ₆ -alkyl or OC ₆ -aryl, very particularly preferably methyl, CF ₃ or O-methyl.

In a very particularly preferred embodiment, the radicals R ¹ to R ^{40 are} independently hydrogen, alkyl, halogen-substituted alkyl, pseudo-halogen, O-alkyl or O-aryl, preferably hydrogen, Cr to Cβ-alkyl, with one or more F atoms substituted C ₁ to C ₆ alkyl, C 2 - to C ₆ alkyl or OC ₆ aryl, particularly preferably methyl, CF ₃ or O-methyl.

The compounds of the formula (I) used according to the invention in one embodiment are diphenylamino-bis (phenoxy) triazine compounds, i. the group X means

m

The groups M, R, T, U and V have the meanings given above.

In a further embodiment, the compounds of the formula (I) are bis (diphenylamino) -phenoxytriazine compounds, ie the group X is

The radicals R ¹⁶ , R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²⁰ , R ²¹ , R ²² , R ²³ , R ²⁴ and R ²⁵ have the meanings given above.

In one embodiment, the compounds of the formula I have the following formulas (Ia), (Ib), (Ic), Id), (Ie) or (If):

wherein the radicals R ² , R ³ , R ⁴ , R ⁷ , R ⁸ , R ⁹ , R ¹¹ , R ¹² , R ¹³ , R ¹⁴ , R ¹⁵ , R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²² , R ²³ .

R 24 _D 27 _D 28 _D 29 _D 34 _D 36 _D 39 _D 40 _D 2 ' _D 3' _D 4 ' _D 7' _D 8 ' _D 9' _D 17 ' _D 18' _D 19 'p22' _D 23 ', FA _J rA _J rA ₁ FA _J rV _J rX _J rA _J rV _J rV _J rX _J rA _J rA _J rA _J rA, rv, R ^{24 ',} R ^34', R ^{36 ',} R ^2a, R ^3a, R ^4a, R ^7a , R ^8a , R ^9a , R ^2b , R ^3b , R ^4b , R ^7b , R ^8b and R ^9b independently of one another have the abovementioned meanings. Preferably mean

R 2 _D 3 _D 4 _D 7 _D 8 _D 9 _D 11 _D 12 D ¹³ D ¹⁴ D ¹⁵ D ¹⁷ D ¹⁸ D ¹⁹ D ²² D ²³ D ²⁴ D ²⁷ D ²⁸ D ²⁹ , rA, rv, rv, rv, rv , rv, rv, rv, rv, r \, r \, rv, rv, rv, rv, rv,

_D 34 _D 36 _D 39 _D 40 _D 2 _D 3 _D 4 _D ⁷ D ⁸ D ⁹ D ¹⁷ D ¹⁸ D ¹⁹ D ²² D ²³ D ²⁴ D ³⁴ D ³⁶ D D ² ' ^a rv, rv, rv,

R ^3a , R ^4a , R ^7a , R ^8a , R ^9a , R ^2b , R ^3b , R ^4b , R ^7b , R ^8b and R ^9b independently of one another are hydrogen, alkyl, halogen-substituted alkyl, pseudohalogen, O-alkyl or O. - Aryl, preferably hydrogen, C ₁ - to C ₆ -alkyl, with one or more F atoms substituted C _r to C ₆ alkyl, Od to C _δ alkyl or OC ₆ -aryl, more preferably methyl, CF ₃ or O-methyl.

Examples of suitable structures of the above formulas are:

The preparation of the diphenylamino-bis (phenoxy) and bis (diphenylamino) -phenoxytriazine compounds of the general formula (I) according to the invention is carried out according to methods known to the person skilled in the art, e.g. by nucleophilic substitution of 2,4,6-trichloro-1, 3,5-triazine with suitable Li-diarylamides, e.g. according to the method mentioned in H. Inomata et al., Chemistry of Materials 2004, 16, 1285 or with suitable phenates, e.g. according to the method mentioned in F.C. Schaefer et al., Journal of the American Chemical Society, 1951, 73, 2990.

In the following Scheme 1, a general reaction scheme is shown by the example of the preparation of a bis (diphenylamino) phenoxytriazine compound of the formula I:

In the following Scheme 2, a general reaction scheme is shown using the example of the preparation of a diphenylamino-bis (phenoxy) triazine compound of the formula I:

General Reaction Scheme 2:

The compounds of the formula (I) are outstandingly suitable for use as matrix materials in organic light-emitting diodes. In particular, they are suitable as matrix materials in the light-emitting layer of the OLEDs, wherein the light-emitting layer preferably contains one or more triplet emitters as emitter compounds.

Furthermore, the compounds of the formula (I) are suitable as hole / exciton blocker material, electron / exciton blocker material, hole injection material, electron injection material, hole conductor material and / or electron conductor material, wherein they preferably together with at least one triplet emitter in the OLED invention are used.

The function of the compounds of the formula (I) as matrix material, preferably in the light-emitting layer, as hole / exciton blocker material, as electron / Excitonenblockermaterial, as a hole injection material, as an electron injection material, as a hole conductor material or as an electron conductor material is inter alia dependent on the electronic properties of the compounds of formula (I), ie the substitution pattern of the compounds of formula (I), as well as the Other of the electronic properties (relative positions of the HOMOs and LUMOs) of the respective layers used in the inventive OLED. Thus, by suitable substitution of the compounds of the formula (I), it is possible to adapt the HOMO and LUMO orbital layers to the further layers used in the OLED according to the invention and thus to achieve a high stability of the OLED and thus a long operating life and good efficiencies to reach.

The principles relating to the relative locations of HOMO and LUMO in the individual layers of an OLED are known to those skilled in the art. The following are the principles by way of example with respect to the properties of the block layer for electrons and the block layer for holes in relation to the light-emitting layer:

The LUMO of the block layer for electrons is higher in energy than the LUMO of the materials used in the light-emitting layer (both of the emitter material and optionally used matrix materials). The greater the energy difference of the LUMOs of the block layer for electrons and the materials in the light emitting layer, the better the electron and / or exciton blocking properties of the block layer for electrons. Suitable substitution patterns of the compounds of the formula (I) which are suitable as electron and / or exciton blocker materials are thus dependent inter alia on the electronic properties (in particular the position of the LUMO) of the materials used in the light-emitting layer.

The HOMO of the block layer for holes is lower in energy than the HOMOs of the materials present in the light-emitting layer (both of the emitter materials and of the optionally present matrix materials). The greater the energy difference of the HOMOs of the block layer for holes and the materials present in the light emitting layer, the better the hole and / or exciton blocking properties of the block layer are for holes. Suitable substitution patterns of the compounds of the formula (I) which are suitable as hole and / or exciton blocker materials are thus dependent inter alia on the electronic properties (in particular the position of the HOMOs) of the materials present in the light-emitting layer.

Comparable considerations concerning the relative position of the HOMOs and LUMOs of the different layers used in the OLED according to the invention apply to the further layers optionally used in the OLED and are known to the person skilled in the art. The energies of the HOMOs and LUMOs of the materials used in the OLED according to the invention can be determined by different methods, for example by solution electrochemistry, eg cyclic voltammetry. In addition, the position of the LUMO of a given material can be calculated from the HOMO determined by ultraviolet photon electron spectroscopy (UPS) and the band gap determined optically by absorption spectroscopy.

Another object of the present invention is thus the use of tris (diphenylamino) -triazine compounds of the formula (I) as a matrix material, preferably as a matrix material in a light-emitting layer of the organic light emitting diode, and / or as a hole / Excitonenblockermaterial, electron / Excitonenblockermaterial, hole injection material, electron injection material, hole conductor material and / or E- lektronenleitermaterial, wherein the compounds of formula (I) are preferably used together with at least one triplet emitter in the organic light emitting diode.

In one embodiment, the compound of the formula (I) is preferably used as the matrix material, with the matrix material particularly preferably being used together with a triplet emitter.

Furthermore, the compounds of the formula (I) can be used in OLEDs both as matrix material and as hole / exciton blocker material, electron / exciton blocker material, hole injection material, electron injection material, hole conductor material and / or electron conductor material. In this case, the matrix material, the hole / exciton blocker material, the electron / exciton blocker material, the hole injection material, the electron injection material, the hole conductor material and / or the electron conductor material may be the same or different compounds of the formula (I).

Another object of the present invention is a light-emitting layer containing at least one compound of formula (I) and at least one emitter compound, wherein the emitter compound is preferably a triplet emitter.

The use of the compounds of the formula (I) as matrix materials in the light-emitting layer of an OLED is likewise a further subject of the present invention.

The use of the compounds of the formula (I) as matrix materials and / or as hole / exciton blocker material, electron / exciton blocker material, hole Injection material, electron injection material, hole conductor material and / or electrical conductor material should not preclude the fact that these compounds themselves also emit light. The matrix materials used according to the invention and / or hole / exciton blocker materials, electron / exciton blocker materials, hole injection materials, electron injection materials, hole conductor materials and / or electron conductor materials of the formula (I) have a tendency to crystallize which is lower than that of conventional materials. Using the compounds of the formula (I), it is possible to provide OLEDs having an improved property profile which manifests itself in improved performance, for example an extended service life, good luminance, high quantum yields, etc.

The organic light-emitting diodes (OLEDs) according to the invention are basically composed of several layers, for example: 1. anode 2. hole conductor layer

3. light-emitting layer

4. Blocking layer for holes / excitons

5. Electron conductor layer

6. cathode

It is also possible from the above-mentioned structure different layer sequences, which are known in the art. For example, it is possible that the OLED does not have all of the mentioned layers, for example an OLED with the layers (1) (anode), (3) (light-emitting layer) and (6) (cathode) is also suitable in which the functions of the layers (2) (hole conductor layer) and (4) (hole / exciton layer layer) and (5) (electron conductor layer) are taken over by the adjacent layers. OLEDs comprising layers (1), (2), (3) and (6) or layers (1), (3), (4), (5) and (6) are also suitable. Furthermore, the OLEDs between the anode (1) and the hole conductor layer (2) can have a block layer for electrons / excitons.

The compounds of formula I can be used as charge-transporting or -blocking materials. However, they are preferably used as matrix materials in the light-emitting layer. The compounds of the formula I can be present as the sole matrix material-without further additives-in the light-emitting layer. However, it is likewise possible that, in addition to the compounds of the formula I used according to the invention, further compounds are present in the light-emitting layer. For example, a fluorescent dye may be present to alter the emission color of the emitter molecule present. Furthermore, a diluent material can be used. This diluent material may be a polymer, for example, poly (N-) vinylcarbazole) or polysilane. However, the diluent material may also be a small molecule, for example 4,4'-N, N'-dicarbazolebiphenyl (CBP = CDP) or tertiary aromatic amines. If a diluent material is used, the proportion of the compounds of the formula I used according to the invention in the light-emitting layer is generally still at least 40% by weight, preferably 50 to 100% by weight, based on the total weight of the compounds of the formula I. and diluents.

If at least one compound of the formula (I) is used together with an emitter compound, preferably together with a triplet emitter, in the light-emitting layer of an OLED, which is particularly preferred, the proportion of the at least one compound of the formula (I) in The light-emitting layer generally 10 to 99 wt .-%, preferably 50 to 99 wt .-%, particularly preferably 70 to 97 wt .-%. The proportion of the emitter compound in the light-emitting layer is generally 1 to 90 wt .-%, preferablyl to 50 wt .-%, particularly preferably 3 to 30 wt .-%, wherein the proportions of the at least one compound of Formula (I) and the at least one emitter compound generally give 100 wt .-%. However, it is also possible for the light-emitting layer to contain, in addition to the at least one compound of the formula (I) and the at least one emitter compound, further substances, for example further diluent material, suitable diluent material being mentioned above.

The individual of the abovementioned layers of the OLED can in turn be composed of 2 or more layers. For example, the hole-transporting layer may be composed of a layer into which holes are injected from the electrode and a layer that transports the holes away from the hole-injecting layer into the light-emitting layer. The electron-transporting layer may also consist of several layers, for example a layer in which electrons are injected through the electrode and a layer which receives electrons from the electron-injecting layer and transports them into the light-emitting layer. These mentioned layers are each selected according to factors such as energy level, temperature resistance and charge carrier mobility, as well as the energy difference of said layers with the organic layers or the metal electrodes. The person skilled in the art is able to choose the structure of the OLEDs in such a way that it is optimally adapted to the organic compounds used according to the invention as emitter substances.

In order to obtain particularly efficient OLEDs, the HOMO (highest occupied molecular orbital) of the hole-transporting layer should be aligned with the working function of the anode and the LUMO (lowest unoccupied molecular orbital) of the electrode. NEN-transporting layer should be aligned with the work function of the cathode.

The anode (1) is an electrode that provides positive charge carriers. For example, it may be constructed of materials including a metal, a mixture of various metals, a metal alloy, a metal oxide, or a mixture of various metal oxides. Alternatively, the anode may be a conductive polymer. Suitable metals include the metals of groups Ib, IVa, Va and VIa of the Periodic Table of the Elements and the transition metals of the group Villa. When the anode is to be transparent, mixed metal oxides of groups IIb, INb and IVb of the Periodic Table of the Elements (old ILJPAC version), for example indium tin oxide (ITO), are generally used. It is also possible that the anode (1) contains an organic material, for example polyaniline, as described for example in Nature, Vol. 357, pages 477 to 479 (June 11, 1992). At least either the anode or the cathode should be at least partially transparent in order to be able to decouple the light formed. The material used for the anode (1) is preferably ITO.

Suitable hole conductor materials for the layer (2) of the OLEDs according to the invention are disclosed, for example, in Kirk-Othmer Encyclopedia of Chemical Technology, 4th Edition, Vol. 18, pages 837 to 860, 1996. Both hole transporting molecules and polymers can be used as hole transport material. Commonly used hole transporting molecules are selected from the group consisting of tris- [N- (1-naphthyl) -N- (phenylamino)] triphenylamine (1-naphDATA), 4,4'-bis [N- (1-naphthyl) -N-phenyl-amino] biphenyl (α-NPD), N, N'-diphenyl-N, N'-bis (3-methylphenyl) - [1, 1'-biphenyl] -4,4'-diamine (TPD ), 1, 1-bis [(di-4-tolylamino) phenyl] cyclohexane (TAPC), N, N'-bis (4-methylphenyl) -N, N'-bis (4-ethylphenyl) - [1, 1 '- (3,3'-dimethyl) biphenyl] -4,4'-diamine (ETPD), tetrakis- (3-methylphenyl) -N, N, N', N'-2,5-phenylenediamine (PDA) , α-phenyl-4-N, N-diphenylaminostyrene (TPS), p- (diethylamino) benzaldehyde diphenylhydrazone (DEH), triphenylamine (TPA), bis [4- (N, N-diethylamino) -2-methylphenyl] (4 -methylphenyl) methane (MPMP), 1-phenyl-3- [p- (diethylamino) styryl] - 5- [p- (diethylamino) phenyl] pyrazoline (PPR or DEASP), 1,2-trans-bis ( 9H-carbazol-9-yl) cyclobutane (DCZB), N, N, N ', N'-tetrakis (4-methylphenyl) - (1, 1'-biphenyl) -4,4'-diamine (TTB), 4 , 4 ', 4 "-tris (N, N-diphenylamino) triphenylamine (TDTA), porphyrin ver compounds and phthalocyanines such as copper phthalocyanines. Usually used hole transporting polymers are selected from the group consisting of polyvinyl carbazoles, (phenylmethyl) polysilanes and polyanilines. It is also possible to obtain hole transporting polymers by doping hole transporting molecules into polymers such as polystyrene and polycarbonate. Suitable hole-transporting molecules are the molecules already mentioned above. Furthermore, in one embodiment, carbene complexes can be used as hole conductor materials, wherein the band gap of the at least one hole conductor material is generally greater than the band gap of the emitter material used. In the context of the present application, band gap is to be understood as the triplet energy. Suitable carbene complexes are, for example, carbene complexes, as described in WO 2005/019373 A2, WO 2006/056418 A2 and WO 2005/1 13704 and in the older European applications EP 06 1 12 228.9 and EP 06 1 12 198.4, which are not prepublished are.

The light-emitting layer (3) contains at least one emitter material. In principle, it may be a fluorescence or phosphorescence emitter, suitable emitter materials being known to the person skilled in the art. Preferably, the at least one emitter material is a phosphorescence emitter. The preferably used Phosphoreszenzmitter compounds are based on metal complexes, in particular the complexes of the metals Ru, Rh, Ir, Os, Pd and Pt, especially the complexes of Ir have gained importance. The compounds of the formula I used according to the invention are particularly suitable for use together with such metal complexes. In one preferred embodiment, the compounds of the formula (I) are used as matrix materials and / or hole / exciton and / or electron / exciton blocker materials. In particular, they are suitable for use as matrix materials and / or hole / exciton and / or electron / exciton blocker materials together with complexes of Ru, Rh, Ir, Os, Pd and Pt, particularly preferred for use with complexes of the present invention Ir suitable.

Suitable metal complexes for use in the inventive OLEDs are e.g. in the documents WO 02/60910 A1, US 2001/0015432 A1, US 2001/0019782 A1, US 2002/0055014 A1, US 2002/0024293 A1, US 2002/0048689 A1, EP 1 191 612 A2, EP 1 191 613 A2 , EP 1 211 257 A2, US 2002/0094453 A1, WO 02/02714 A2, WO 00/70655 A2, WO 01/41512 A1, WO 02/15645 A1, WO 2005/019373 A2, WO 2005/1 13704 A2, WO 2006/1 15301 A1, WO 2006/067074 A1 and WO 2006/056418.

Further suitable metal complexes are the commercially available metal complexes tris (2-phenylpyridine) iridium (III), iridium (III) tris (2- (4-tolyl) pyridinato-N, C ² '), iridium (III) tris (1 phenylisoquinoline), iridium (III) to (2-2'-benzothienyl) pyridinato

N, C ³ ') (acetylacetonate), iridium (III) bis (2- (4,6-difluorophenyl) pyridinato-N, C ² ) picolinate, iridium (III) bis (1-phenylisoquinoline) (acetylacetonate), iridium ( III) bis (di-benzo [f, h] quinoxaline) (acetylacetonate), iridium (III) bis (2-methyldi-benzo [f, h] quinoxaline) - (acetylacetonate) and tris (3-methyl-1-phenyl -4-trimethyl-acetyl-5-pyrazoline) terbium (III). The following commercially available materials are also suitable: tris (dibenzoylacetonato) mono (phenanthroline) europium (III), tris (dibenzoylmethane) mono (phenanthroline) europium (III), tris (dibenzoylmethane) mono (5-aminophenan) throline) europium (III), tris (di-2-naphthoylmethane) -mono (phenanthroline) -europium (III), tris (4-bromobenzoylmethane) -mono (phenanthroline) -europium (III), tris (di-biphenylmethane ) mono (phenanthroline) europium (III), tris (dibenzoylmethane) mono (4,7-diphenylphenanthroline) europium (III), tris (dibenzoylmethane) mono (4,7-dimethylphenanthroline) europium (III), tris (dibenzoylmethane) mono (4,7-dimethyl-phenanthroline-disulfonic acid) europium (III) disodium salt, tris [di (4- (2- (2-ethoxyethoxy) ethoxy) benzoylmethane)] mono (phenanthroline) europium (III) and tris [di [4- (2- (2-ethoxyethoxy) ethoxy) benzoylmethane]] mono- (5-aminophenanthroline) europium (III).

Particularly preferred triplet emitters are carbene complexes. In a preferred embodiment of the present invention, the compounds of the formula (I) are used in the light-emitting layer as matrix material together with carbene complexes as triplet emitters. Suitable carbene complexes are known to the person skilled in the art and are mentioned in some of the aforementioned applications and below. In a further preferred embodiment, the compounds of the formula (I) are used as hole / exciton blocker material together with carbene complexes as triplet emitters. The compounds of the formula (I) can furthermore be used both as matrix materials and as hole / exciton blocker materials together with carbene complexes as triplet emitters.

Suitable metal complexes for use together with the compounds of formula I as matrix materials and / or hole / exciton and / or electron / exciton blocker materials in OLEDs are thus e.g. also carbene complexes, as described in WO 2005/019373 A2, WO 2006/056418 A2 and WO 2005/1 13704 and in the earlier unpublished PCT applications WO 2007/1 15970 and WO

2007/1 15981 are described. The disclosure of said WO and EP applications is hereby explicitly incorporated by reference and these disclosures are to be considered incorporated into the content of the present application.

The block layer for holes / excitons (4) can typically comprise hole blocker materials used in OLEDs, such as 2,9-dimethyl-4,7-diphenyl-1, 10-phenanthroline (bathocuproine, (BCP)), bis (2-methyl-8 -quinolinato) -4-phenyl-phenylato) -aluminium (III) (BAIq), phenothiazine-S, S-dioxide derivatives and 1,3,5-tris (N-phenyl-2-benzylimidazole) -benzene) (TPBI), wherein TPBI and BAIq are also suitable as electron-conducting materials. In a further embodiment, compounds containing aromatic or heteroaromatic groups containing groups via carbonyl groups, as disclosed in WO2006 / 100298, can be used as a blocking layer for solvents. cher / excitons (4) or as matrix materials in the light-emitting layer (3) are used.

In a preferred embodiment, the present invention relates to an OLED according to the invention comprising the layers (1) anode, (2) hole conductor layer, (3) light-emitting layer, (4) block layer for holes / excitons, (5) electron conductor layer and (6) cathode, and optionally further layers, wherein the block layer for holes / excitons contains at least one compound of formula (I).

In a further preferred embodiment, the present invention relates to an OLED according to the invention comprising the layers (1) anode, (2) hole conductor layer, (3) light-emitting layer, (4) block layer for holes / excitons, (5) electron layer and 6) cathode, and optionally further layers, wherein the light-emitting layer (3) contains at least one compound of formula (I) and the block layer for holes / excitons at least one compound of formula (I).

In a further embodiment, the present invention relates to an OLED according to the invention comprising the layers (1) anode, (2) hole conductor layer and / or (2 ') blocking layer for electrons / excitons (the OLED can comprise both the layers (2) and (2') and either the layer (2) or the layer (2 ')), (3) light-emitting layer, (4) block layer for holes / excitons, (5) electron conductor layer and (6) cathode, and optionally further layers, wherein the the block layer for electrons / excitons and / or the hole conductor layer and optionally the light-emitting layer (3) contains at least one compound of the formula (I).

Suitable electron conductor materials for the layer (5) of the O-LEDs according to the invention comprise chelated metals with oxinoid compounds, such as tris (8-quinolinolato) aluminum (Alqβ), bis (2-methyl-8-quinolinato) -4-phenyl-phenylato ) - aluminum (III) (BAIq), phenanthroline-based compounds such as 2,9-dimethyl-4,7-diphenyl-1, 10-phenanthroline (DDPA = BCP) or 4,7-diphenyl-1,10-phenanthroline (DPA and azole compounds such as 2- (4-biphenylyl) -5- (4-t-butylphenyl) -1, 3,4-oxadiazole (PBD) and 3- (4-biphenylyl) -4-phenyl-5- (4- t-butylphenyl) -1,2,4-triazole (TAZ) and 2,2 ', 2 "- (1,3,5-phenylene) tris [1-phenyl-1H-benzimidazole] (TPBI) For example, layer (5) may serve to facilitate electron transport as well as a buffer layer or barrier layer to avoid quenching of the exciton at the interfaces of the layers of the OLED Preferably layer (5) improves the mobility of the electrons and reduces quenching Excitons Conductor materials are TPBI and BAIq.

Of the materials mentioned above as hole conductor materials and electron conductor materials, some may fulfill several functions. For example, some are the electron-conducting materials at the same time hole-blocking materials, if they have a low-lying HOMO. These can be z. In the block layer for holes / excitons (4). However, it is also possible that the function as a hole / exciton blocker of the layer (5) is taken over, so that the layer (4) may be omitted.

The charge transport layers can also be electronically doped in order to improve the transport properties of the materials used, on the one hand to make the layer thicknesses more generous (avoidance of pinholes / short circuits) and on the other hand to minimize the operating voltage of the device. For example, the hole conductor materials can be doped with electron acceptors, for example phthalocyanines or arylamines such as TPD or TDTA can be doped with tetrafluorotetracyanchinodimethane (F4-TCNQ). The electron conductor materials can be doped, for example, with alkali metals, for example Alq ₃ with lithium. The electronic doping is known to the person skilled in the art and described, for example, in W. Gao, A. Kahn, J. Appl. Phys., Vol. 94, no. 1, 1 July 2003 (p-doped organic layers); AG Werner, F. Li, K. Harada, M. Pfeiffer, T. Fritz, K. Leo. Appl. Phys. Lett., Vol. 82, no. 25, 23 June 2003 and Pfeiffer et al., Organic Electronics 2003, 4, 89-103.

The cathode (6) is an electrode which serves to introduce electrons or negative charge carriers. Suitable materials for the cathode are selected from the group consisting of alkali metals of group Ia, for example Li, Cs, alkaline earth metals of group IIa, for example calcium, barium or magnesium, metals of group IIb of the Periodic Table of the Elements (old ILJPAC version) comprising the lanthanides and actinides, for example samarium. Furthermore, metals such as aluminum or indium, as well as combinations of all the metals mentioned can be used. Furthermore, lithium-containing organometallic compounds or LiF can be applied between the organic layer and the cathode to reduce the operating voltage.

The OLED according to the present invention may additionally contain further layers which are known to the person skilled in the art. For example, a layer can be applied between the layer (2) and the light-emitting layer (3), which facilitates the transport of the positive charge and / or adapts the band gap of the layers to one another. Alternatively, this further layer can serve as a protective layer. In an analogous manner, additional layers may be present between the light-emitting layer (3) and the layer (4) to facilitate the transport of the negative charge and / or to match the band gap between the layers. Alternatively, this layer can serve as a protective layer. In a preferred embodiment, in addition to the layers (1) to (6), the OLED according to the invention contains at least one of the further layers mentioned below:

^~ A hole injection layer between the anode (1) and the hole-transporting layer (2); a block layer for electrons between the hole-transporting layer (2) and the light-emitting layer (3); an electron injection layer between the electron-transporting layer (5) and the cathode (6).

The person skilled in the art knows how to select suitable materials (for example based on electrochemical investigations). Suitable materials for the individual layers are known to those skilled in the art and e.g. in WO 00/70655.

Furthermore, it is possible that some or all of the layers used in the O-LED according to the invention are surface-treated in order to increase the efficiency of the charge carrier transport. The selection of materials for each of said layers is preferably determined by obtaining an OLED having a high efficiency and lifetime.

The preparation of the OLEDs according to the invention can be carried out by methods known to the person skilled in the art. In general, the OLED according to the invention is produced by successive vapor deposition of the individual layers onto a suitable substrate. Suitable substrates are for example glass, inorganic semiconductors or polymer films. For vapor deposition, conventional techniques can be used such as thermal evaporation, chemical vapor deposition (CVD), physical vapor deposition (PVD) and others. In an alternative method, the organic layers of the OLED can be applied from solutions or dispersions in suitable solvents, using coating techniques known to those skilled in the art.

In general, the various layers have the following thicknesses: anode (1) 50 to 500 nm, preferably 100 to 200 nm; Hole-conductive layer (2) 5 to 100 nm, preferably 20 to 80 nm, light-emitting layer (3) 1 to 100 nm, preferably 10 to 80 nm, block layer for holes / excitons (4) 2 to 100 nm , preferably 5 to 50 nm, electron-conducting layer (5) 5 to 100 nm, preferably 20 to 80 nm, cathode (6) 20 to 1000 nm, preferably 30 to 500 nm. The relative position of the recombination zone of holes and electrons in The OLED according to the invention with respect to the cathode and thus the emission spectrum of the OLED can be influenced inter alia by the relative thickness of each layer. This means the thickness of the electron transport layer should preferably be chosen so that the position of the recombination zone is tuned to the optical resonator property of the diode and thus to the emission wavelength of the emitter. The ratio of the layer thicknesses of the individual layers in the OLED depends on the materials used. The layer thicknesses of any additional layers used are known to the person skilled in the art. It is possible that the electron-conducting layer and / or the hole-conducting layer have larger thicknesses than the specified layer thicknesses when they are electrically doped.

According to the invention, the light-emitting layer and / or at least one of the further layers optionally present in the OLED according to the invention contains at least one compound of the general formula (I). While the at least one compound of the general formula (I) is present in the light-emitting layer as the matrix material, the at least one compound of the general formula (I) in the at least one further layer of the inventive OLED can each alone or together with at least one of the others for the corresponding layers suitable materials mentioned above are used. It is also possible for the light-emitting layer to contain, in addition to the compound of the formula (I), one or more further matrix materials.

The efficiency of the OLEDs of the invention may be e.g. be improved by optimizing the individual layers. For example, highly efficient cathodes such as Ca or Ba, optionally in combination with an intermediate layer of LiF, can be used. Shaped substrates and new hole-transporting materials, which cause a reduction in the operating voltage or an increase in the quantum efficiency, can also be used in the inventive OLEDs. Furthermore, additional layers may be present in the OLEDs to adjust the energy levels of the various layers and to facilitate electroluminescence. The OLEDs according to the invention can be used in all devices in which electroluminescence is useful. Suitable devices are preferably selected from stationary and mobile screens and lighting units. Stationary screens are e.g. Screens of computers, televisions, screens in printers, kitchen appliances and billboards, lights and signboards. Mobile screens are e.g. Screens in cell phones, laptops, digital cameras, vehicles, and destination displays on buses and trains.

Furthermore, the compounds of formula I can be used in OLEDs with inverse structure. The compounds of the formula I used according to the invention in these inverse OLEDs are preferably used in turn as matrix materials in the light-emitting layer. The construction of inverse OLEDs and the materials usually used therein are known to the person skilled in the art. The following examples further illustrate the invention.

Examples

1.) Syntheses

Example a): Triply substitution of 2,4,6-trichloro-1,3,5-triazine (cyanuric chloride) to give 2,4,6-tris (diphenylamino) -1,3,5-triazine (1) (Comparison )

AIIg. Method A: 5.92 g (35 mmol) of diphenylamine are dissolved in a 250 ml 2-neck flask equipped with nitrogen inlet and septum in 100 ml of THF dried over potassium under a nitrogen atmosphere. The solution is then treated at room temperature over a period of 10 minutes with 21.8 ml (35 mmol) of n-butyllithium (1.6M in hexane) and stirred for a further 10 minutes. In a 500 ml 3-necked flask, equipped with nitrogen inlet, reflux condenser and septum, 1.84 g (10 mmol) of cyanuric chloride in 100 ml of potassium-dried THF under nitrogen atmosphere, dissolved. The lithium-diphenylamine solution is added dropwise to the cyanuric chloride solution by means of a transfer cannula. The reaction mixture is then refluxed for 6 hours. After cooling to room temperature, the solvent is evaporated and the residue is stirred for 10 minutes in 200 ml of water. The white solid obtained by filtration is washed with diethyl ether, slurried in hot ethanol and filtered while hot. For further purification, the product is recrystallized in chlorobenzene and dried under high vacuum to obtain 3.55 g (61%) of 2,4,6-tris (diphenylamino) -1, 3,5-triazine (1) as a white solid. 1H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 7.09-7.16 (m, 24H), 7.02-7.06 (m, 6H). EI-MS: m / z = 582 (M ⁺ ) Example b): Triply Substituted 2,4,6-trichloro-1,3,5-triazine to give 2, 4, 6-tris (3-methyldiphenylamino) -1,3,5-triazine (2) (comparative)

6.41 g (35 mmol) of 3-methyldiphenylamine are reacted with 1.84 g (10 mmol) of cyanuric chloride according to procedure A and purified, giving 3.81 g (64%) of 2,4,6-tris (3-methyldiphenylamino) -1,3 , 5-triazine (2) can be obtained as a white solid. 1H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 7.08-7.15 (m, 9H), 6.82-7.05 (m, 18H), 2.17 (s, 9H). EI-MS: m / z = 624 (M ⁺ ).

Example c): Twofold substitution of 2,4,6-trichloro-1,3,5-triazine (cyanuric chloride) to give 2,4-bis (diphenylamino) -6-chloro-1,3,5-triazine

AIIg. Method A: 3.38 g (20 mmol) of diphenylamine are dissolved in a 250 ml 2-necked flask equipped with nitrogen inlet and septum in 100 ml of potassium-dried THF under a nitrogen atmosphere. Subsequently, the solution is treated at room temperature over a period of 10 minutes with 12.5 ml (20 mmol) of n-butyllithium (1.6M in hexane) and stirred for a further 10 minutes. In a 500 ml 3-necked flask, equipped with nitrogen inlet, reflux condenser and septum, 1.84 g (10 mmol) of cyanuric chloride in 100 ml of potassium-dried THF under a nitrogen atmosphere, dissolved. The lithium diphenylamine solution is separated by means of a transfer cannula added drop by drop to the cyanuric chloride solution. The reaction mixture is then refluxed for 6 hours. After cooling to room temperature, the solvent is evaporated and the residue is stirred for 10 minutes in 200 ml of water. The white solid obtained by filtration is washed with diethyl ether, slurried in hot ethanol and filtered while hot. The product is then purified by column chromatography with a hexane / THF eluant mixture (3/1, v / v) to give 3.48 g (77%) of 2,4-bis (diphenylamino) -6-chloro-1,3,5-triazine as a white solid.

¹ H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 7.22-7.33 (m, 8H), 7.05-7.21 (m, 12H). EI-MS: m / z = 448 (M ⁺ ).

Substituting 2,4-bis (diphenylamino) -6-chloro-1,3,5-triazine to give 2,4-bis (diphenylamino) -6- (3,5-dimethylphenoxy) -1,3,5 triazine (3) (according to the invention)

2.25 g (5 mmol) of 2,4-bis (diphenylamino) -6-chloro-1, 3,5-triazine are reacted with 0.79 g (6.5 mmol) of 3,5-dimethylphenol according to procedure B and purified, where 2.15 g (80%) of 2,4-bis (diphenylamino) -6- (3,5-dimethylphenoxy) -1, 3,5-triazine (3) is obtained as a white solid.

¹ H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 7.15-7.24 (m, 12H), 7.07-7.15 (m, 8H), 2.21 (s, 6H). EI-MS: m / z = 534 (M ⁺ ).

Example d):

Two-fold substitution of 2,4,6-trichloro-1,3,5-triazine (cyanuric chloride) to give 2,4-bis (phenoxy) -6-chloro-1,3,5-triazine

3.76 g (20 mmol) of cyanuric chloride are in a 500 ml 2-necked flask fitted with dropping funnel and thermometer, dissolved in 100 ml of acetone and cooled to 10 ⁰ C. In a 250 ml flask, 3.76 g (40 mmol) of phenol are dissolved in 150 ml of acetone / water mixture (1/4, v / v), treated with 1.60 g (40 mmol) of sodium hydroxide and stirred for 15 minutes at room temperature. Subsequently, the sodium phenolate solution of the cyanuric chloride solution is added dropwise over a period of 30 minutes, the solution temperature must not exceed 10 ⁰ C. The reaction solution is then stirred for 1 hour at 10 ⁰ C and then warmed to room temperature over a period of 2 hours. The resulting white solid is filtered off and washed twice with 50 ml of water. For further purification, the product is recrystallized in a hexane / THF mixture (1/1, v / v) and dried in vacuo, giving 4.78 g (80%) of 2,4-bis (phenoxy) -6-chloro-1, 3 , 5-triazine can be obtained as a white solid. 1 H NMR (250 MHz, CDCl ₃ ) δ (ppm): 7.33-7.44 (m, 4H), 7.21-7.30 (m, 2H), 7.09-7.16 (d, 4H). EI-MS: m / z = 298 (M ⁺ ).

Substituting 2,4-bis (phenoxy) -6-chloro-1,3,5-triazine to give 2,4-bis (phenoxy) -6- (3-methyldiphenylamino) -1,3,5-triazine ( 4) (according to the invention)

1.34 g (7.3 mmol) of 3-methyldiphenylamine are mixed with 1.79 g (6 mmol) of 2,4-bis (phenoxy) -6-chloro-1,3,5-triazine according to AIIg. Regulation A reacted. The product is purified by column chromatography with a hexane / THF eluent. onsmittelgemisch (10/1, V / V), whereby 1.35 g (51%) of 2,4-bis (phenoxy) -6- (3-methyldiphenylamino) -1, 3,5-triazine (4) are obtained as a white solid , 1H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 7.12-7.24 (m, 10H), 7.03-7.12 (m, 6H), 6.93-7.01 (m, 3H), 2.24 (s, 3H). EI-MS: m / z = 446 (M ⁺ ).

Example e): Substitution of 2,4-bis (diphenylamino) -6-chloro-1,3,5-triazine to give 2,4-bis (diphenylamino) -6-phenoxy-1,3,5-triazine ( 5) (according to the invention)

AIIg. Protocol B: 2.25 g (5 mmol) of 2,4-bis (diphenylamino) -6-chloro-1,3,5-triazine are dissolved in 70 ml of acetone in a 250 ml 2-necked flask equipped with reflux condenser and dropping funnel. 0.61 g (6.5 mmol) of phenol are dissolved in 50 ml of acetone / water mixture (1/1, v / v) in a 100 ml flask, mixed with 0.23 g (5.75 mmol) of sodium hydroxide and stirred for 15 minutes at room temperature. Subsequently, the sodium phenolate solution is added dropwise to the 2,4-bis (diphenylamino) -6-chloro-1,3,5-triazine solution over a period of 15 minutes. The reaction solution is then boiled under reflux for 8 hours. After cooling to room temperature, 50 ml of water are added to the solution. The white solid is filtered off and washed twice with 30 ml of water. The resulting product is purified by column chromatography with a hexane / ethyl acetate eluant mixture (7/1, v / v) to give 1.65 g (65%) of 2,4-bis (diphenylamino) -6-phenoxy-1,3,5 triazine (5) can be obtained as a white solid. ¹ H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 7.10-7.23 (m, 20H), 6.99-7.08 (m, 5H). EI-MS: m / z = 506 (M ⁺ ).

Example f):

Two-fold substitution of 2,4,6-trichloro-1, 3,5-triazine to give 2,4-bis (3-methyldiphenylamino) -6-chloro-1,3,5-triazine

3.66 g (20 mmol) of 3-methyldiphenylamine are reacted with 1.84 g (10 mmol) of cyanuric chloride in accordance with procedure A. The product is purified by column chromatography with a hexane / THF eluent mixture (7/1, V / V), giving 3.72 g (78%) of 2,4-bis (3-methyldiphenylamino) -6-chloro-1, 3.5 Triazine be obtained as a white solid.

¹ H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 7.07-7.16 (m, 6H), 6.81-7.05 (m, 12H), 2.17 (s, 6H).

EI-MS: m / z = 477 (M ⁺ ).

Substituting 2,4-bis (3-methyldiphenylamino) -6-chloro-1,3,5-triazine to give 2,4-bis (3-methyldiphenylamino) -6- (3,5-dimethylphenoxy) -1, 3, 5-triazine (6) (according to the invention)

2.39 g (5 mmol) of 2,4-bis (3-methyldiphenylamino) -6-chloro-1,3,5-triazine are reacted with 0.79 g (6.5 mmol) of 3,5-dimethylphenol according to procedure B and purified, to give 2.03 g (72%) of 2,4-bis (3-methyldiphenylamino) -6- (3,5-dimethylphenoxy) -1,3,5-triazine as a white solid (6). 1H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 7.04-7.19 (m, 12H), 6.88-7.01 (m, 6H), 6.64-6.72 (m, 3H), 2.21 (s, 6H), 2.19 (s, 6H). EI-MS: m / z = 562 (M ⁺ ).

Example g):

Two-fold substitution of 2,4,6-trichloro-1,3,5-triazine to give 2,4-bis (4,4'-dimethyldiphenylamino) -6-chloro-1,3,5-triazine

3.95 g (20 mmol) of 4,4'-dimethyldiphenylamine are reacted with 1.84 g (10 mmol) of cyanuric chloride in accordance with Procedure A. The product is purified by column chromatography with a hexane / THF eluent mixture (4/1, V / V), giving 2.56 g (51%) of 2,4-bis (4,4'-dimethyldiphenylamino) -6-chloro-1, 3,5-triazine can be obtained as a white solid.

¹ H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 6.88-7.05 (m, 16H), 2.22 (s, 12H). EI-MS: m / z = 505 (M ⁺ ).

Substitution of 2,4-bis (4,4'-dimethyldiphenylamino) -6-chloro-1,3,5-triazine to give 2,4-bis (4,4'-dimethyldiphenylamino) -6- (3,5 -dimethylphenoxy) -1, 3, 5-triazine (7) (according to the invention)

2.53 g (5 mmol) of 2,4-bis (4,4'-dimethyldiphenylamino) -6-chloro-1,3,5-triazine are reacted with 0.79 g (6.5 mmol) of 3,5-dimethylphenol according to procedure B and purified by sublimation to give 2.66 g (90%) of 2,4-bis (4,4'-dimethyldiphenylamino) -6- (3,5-dimethylphenoxy) -1, 3,5-triazine as a white solid.

¹ H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 6.92-7.08 (m, 16H), 6.65-6.71 (m, 3H), 2.28 (s, 12H), 2.20 (s, 6H). EI-MS: m / z = 590 (M ⁺ ).

Example h):

Goldberg reaction for the preparation of 9- (4-methoxyphenyl) carbazole

CuI, DACy, dioxane

3.35 g (20 mmol) of carbazole, 5.15 g (22 mmol) of 4-iodoanisole, 0.38 g (2 mmol) of copper iodide and 4.24 g (20 mmol) of potassium phosphate in a 250 ml 2-necked flask equipped with nitrogen inlet and reflux condenser, in 70 ml of dry dioxane under nitrogen atmosphere, dissolved. 0.23 g (2 mmol) of trans-1, 2-diaminocyclohexane (DACy) are added before the reaction solution is stirred for 24 hours at 1 10 ⁰ C under reflux. After cooling to room temperature, the inorganic salts are separated on an Alox N column. The resulting filtrate is concentrated and the product purified by column chromatography with a cyclohexane / THF eluent mixture (20/1, v / v). 3.12 g (58%) of 9- (4-methoxyphenyl) carbazole are obtained as a white solid.

¹ H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 8.15 (d, 2H), 7.48-7.26 (m, 8H); 7.12 (m, 2H); 3.93 (s, 3H).

EI-MS: m / z = 273 (100, M ⁺ ).

Ether cleavage to prepare 9- (4-hydroxyphenyl) carbazole

2.00 g (7.33 mmol) of 9- (4-methoxyphenyl) -carbazole are dissolved in a 100 ml 2-necked flask equipped with nitrogen inlet and septum in 40 ml of dry dichloromethane under a nitrogen atmosphere and cooled to -78 ° C. While stirring, 8 ml (8 mmol) of boron tribromide solution (1 M in CH ₂ Cl ₂ ) are slowly added dropwise. The reaction solution is warmed to room temperature over a period of 12 hours. After the addition of 20 ml of water, the organic phase is separated, washed twice with water and concentrated. The product is purified by column chromatography with a cyclohexane / THF eluent mixture (10/1, v / v). 1.75 g (93%) of 9- (4-hydroxyphenyl) carbazole are obtained as a white solid.

¹ H-NMR (250 MHz): δ (ppm) 8.04 (d, 2H); 7.34-7.14 (m, 8H), 6.96-6.92 (m, 2H); 4.97 (s, 1H).

EI-MS: m / z = 259 (100, M ⁺ ).

Substituting 2,4-bis (4,4'-dimethyldiphenylamino) -6-chloro-1,3,5-triazine to give 2,4-bis (4,4'-dimethyldiphenylamino) -6- (4- (4-bis) carbazol-9-yl) -phenoxy) -1,3,5-triazine (8) (according to the invention)

1.01 g (2 mmol) of 2,4-bis (4,4'-dimethyldiphenylamino) -6-chloro-1,3,5-triazine are treated with 0.63 g (2.4 mmol) of 9- (4-hydroxyphenyl) carbazole according to instructions B and purified by column chromatography with a hexane / THF eluant mixture (10/1, v / v) to give 1.10 g (76%) of 2,4-bis (4,4'-dimethyldiphenylamino) -6- (4-10 g). (carbazol-9-yl) -phenoxy) -1, 3,5-triazine (8) can be obtained as a white solid. ¹ H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 8.14 (d, 2H), 7.34-7.45 (m, 4H), 7.25-7.31 (m, 6H), 6.93-7.10 (m, 16H), 2.24 (s, 12H).

Example h):

Goldberg reaction for the preparation of 9- (4-methoxyphenyl) carbazole

CuI, DACy, dioxane

EI-MS: m / z = 273 (100, M ⁺ ).

Ether cleavage to prepare 9- (4-hydroxyphenyl) carbazole

2.00 g (7.33 mmol) of 9- (4-methoxyphenyl) -carbazole are dissolved in a 100 ml 2-necked flask equipped with nitrogen inlet and septum in 40 ml of dry dichloromethane under a nitrogen atmosphere and cooled to -78 ° C. While stirring, 8 ml (8 mmol) of boron tribromide solution (1 M in CH ₂ Cl ₂ ) are slowly added dropwise. The reaction solution is warmed to room temperature over a period of 12 hours. After the addition of 20 ml of water, the organic phase is separated, washed twice with water and concentrated. The product is purified by column chromatography a cyclohexane / THF eluant mixture (10/1, v / v). 1.75 g (93%) of 9- (4-hydroxyphenyl) carbazole are obtained as a white solid.

¹ H-NMR (250 MHz): δ (ppm) 8.04 (d, 2H); 7.34-7.14 (m, 8H), 6.96-6.92 (m, 2H); 4.97 (s, 1H). EI-MS: m / z = 259 (100, M ⁺ ).

1.01 g (2 mmol) of 2,4-bis (4,4'-dimethyldiphenylamino) -6-chloro-1,3,5-triazine are treated with 0.63 g (2.4 mmol) of 9- (4-hydroxyphenyl) carbazole according to instructions B was reacted and purified by column chromatography with a hexane / THF eluent mixture (10/1, v / v), giving 1.10 g (76%) of 2,4-bis (4,4'-dimethyldiphenylamino) -6- ( 4- (carbazol-9-yl) -phenoxy) -1, 3,5-triazine (8) can be obtained as a white solid. ¹ H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 8.14 (d, 2H), 7.34-7.45 (m, 4H), 7.25-7.31 (m, 6H), 6.93-7.10 (m, 16H), 2.24 (s, 12H).

Example (i):

Goldberg reaction for the preparation of 3, 6-dimethyl-9- (4-methoxyphenyl) carbazole

\ CuI, DACy, dioxane 3.91 g (20 mmol) of 3,6-dimethylcarbazole, 5.15 g (22 mmol) of 4-iodoanisole, 0.38 g (2 mmol) of copper iodide and 4.24 g (20 mmol) of potassium phosphate are placed in a 250 ml 2-necked flask equipped with nitrogen inlet and Reflux condenser, in 70 ml of dry dioxane under a nitrogen atmosphere. 0.23 g (2 mmol) of trans-1, 2-diaminocyclohexane (DACy) are added before the reaction solution is stirred for 24 hours at 1 10 ⁰ C under reflux. After cooling to room temperature, the inorganic salts are separated on an Alox N column. The resulting filtrate is concentrated and the product is purified by column chromatography with a cyclohexane / THF eluent mixture (20/1, v / v). 4.45 g (74%) of 3,6-dimethyl-9- (4-methoxyphenyl) carbazole are obtained as a white solid.

¹ H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 7.89 (s, 2H), 7.46-7.40 (m, 2H), 7.22-7.18 (m, 4H), 7.12-7.06 (m, 2H), 3.91 (s, 3H), 2.54 (s, 6H).

EI-MS: m / z = 301 (100, M ⁺ ).

Ether cleavage to give 3,6-dimethyl-9- (4-hydroxyphenyl) carbazole

1.52 g (5.0 mmol) of 3,6-dimethyl-9- (4-methoxyphenyl) -carbazole are dissolved in 40 ml of 2-neck flask equipped with nitrogen inlet and septum in 40 ml of dry dichloromethane under a nitrogen atmosphere and Cooled to 78 ° C. While stirring, 5.5 ml (5.5 mmol) of boron tribromide solution (1 M in CH ₂ Cl ₂ ) are slowly added dropwise. The reaction solution is warmed to room temperature over a period of 12 hours. After the addition of 20 ml of water, the organic phase is separated, washed twice with water and concentrated. The product is purified by column chromatography with a cyclohexane / THF eluent mixture (10/1, v / v). 1.43 g (99%) of 3,6-dimethyl-9- (4-hydroxyphenyl) carbazole are obtained as a white solid.

¹ H-NMR (250 MHz): δ (ppm) 7.89 (s, 2H), 7.40-7.35 (m, 2H), 7.22-7.18 (m, 4H), 7.04-6.98 (m, 2H), 5.07 (s , 1H), 2.54 (s, 6H).

EI-MS: m / z = 273 (100, M ⁺ ).

Substituting 2,4-bis (diphenylamino) -6-chloro-1,3,5-triazine to give 2,4-bis (diphenylamino) -6- (4- (3,6-dimethyl-carbazole-9- yl) phenoxy) -1, 3, 5-triazine (9)

2.07 g (4.6 mmol) of 2,4-bis (diphenylamino) -6-chloro-1,3,5-triazine are reacted with 1.38 g (4.8 mmol) of 3,6-dimethyl-9- (4-hydroxyphenyl) carbazole Rule B and purified by column chromatography with a hexane / THF eluent mixture (10/1, v / v) to give 2.61 g (81%) of 2,4-bis (diphenylamino) -6- (4- (3,6-dimethyl-carbazol-9-yl) -phenoxy) -1, 3,5-triazine (9) can be obtained as a white solid. ¹ H-NMR (250 MHz, CDCl ₃ ) δ (ppm): 7.90 (s, 2H), 7.34-7.30 (m, 2H), 7.25-7.18 (m, 20H), 7.17-7.12 (m, 6H), 2.56 (s, 6H).

2.) Thermal properties

All the thermal data listed in the table below were measured by means of differential scanning calorimetry (DSC) on a Perkin-Elmer DSC-7 calorimeter with a heating or cooling rate of 10 K / min under inert gas.

The chemical structural formulas of the individual triazine derivatives are listed below.

Thermal properties of diphenylamino bis (phenoxy) - and bis (diphenylamino) phenoxytriazine compounds of the general formula

(I)

crystallization

Ex. Connection T _m [° C] ¹⁾ T _C [° C] ²⁾ τ _rec [° c] ³⁾ Tg [ ⁰ Cf of films h) 1 (comparison) 309 265 208 - Immediately i) 2 (comparison) 175 102 119 - 1 day k) 3 (according to the invention) 183 - 116 54> 90 days

I) 4 (according to the invention) 143-40> 90 days 1) melting point

2) crystallization temperature

3) recrystallization temperature 4) glass transition temperature lamino) -1, 3,5-triazine (1)

ldiphenylamino) -1, 3,5-triazine

) -6- (3,5-dimethyl- (3) (according to the invention)

2,4-bis (phenoxy) -6- (3-methyldiphenylamino) -1,3,5-triazine (4) (according to the invention) M = 446 g / mol 3.) diodes

Example m):

Preparation of an OLED containing 2,4-bis (diphenylamino) -6- (3,5-dimethylphenoxy) -1,3,5-triazine (3) as matrix material (according to the invention)

The ITO substrate used as anode is first cleaned in an acetone / isopropanol mixture in an ultrasonic bath. To remove any organic residues, the substrate is cleaned for a further 10 minutes in the O ₂ plasma.

Thereafter, the below-mentioned organic materials at a rate of about 0.5-5 nm / min at 10 ^"6 mbar are vapor-deposited on the cleaned substrate. The hole conductor and exciton is N, N'-di (naphth-1-yl) -N , N'-diphenyl-benzidine (α-NPD) (V1) is applied to the substrate at a thickness of 30 nm.

α-NPD (V1)

Subsequently, a mixture of 10 wt .-% of the compound iridium (III) -bis [(4,6-difluorophenyl) -pyridinato-N, C2 '] picolinate (Flrpic) (V2) and 90 wt .-% of the compound. 2 , 4-bis (diphenylamino) -6- (3,5-dimethylphenoxy) -1, 3,5-triazine (3) evaporated to a thickness of 30 nm, the former compound acts as an emitter, the latter as a matrix material.

Flrpic (V2)

Next, the electron transporter and exciton / hole blocker bis (2-methyl-8-quinolinolato) -4- (phenylphenolato) aluminum (III) (BAIq) (V3) in a thickness of 30 nm, followed by a 1 nm thick lithium fluoride Layer and finally vapor deposited a 200 nm thick aluminum electrode.

BAIq (V3)

N, N'-di (naphth-1-yl) -N _! N'-diphenyl-benzidine (α-NPD) (V1), iridium (III) -bis [(4,6-difluorophenyl) -pyridinato-N, C2 '] picolinate (Flrpic) (V2) and bis (2-methyl -8-quinolinolato) -4- (phenylphenolato) aluminum (III) (BAIq) (V3) are commercially available.

To characterize the OLED, electroluminescence spectra are recorded at different currents or voltages. Furthermore, the current-voltage characteristic in combination with the emitted light quantity is measured with a luminance meter.

For the described OLED, the following electro-optical data result:

Example n):

Preparation of an OLED containing 2,4-bis (phenoxy) -6- (3-methyldiphenylamino) -1,3,5-triazine (4) as matrix material (according to the invention)

Thereafter, the below-mentioned organic materials at a rate of about 0.5-5 nm / min at about 10 ^"6 mbar are vapor-deposited on the cleaned substrate as a hole conductor and exciton is N, N'-di (naphth-1-yl). - N, N'-diphenyl-benzidine (α-NPD) (V1) was applied to the substrate at a thickness of 30 nm.

Subsequently, a mixture of 10 wt .-% of the compound iridium (III) -bis [(4,6-difluorophenyl) -pyridinato-N, C2 '] picolinate (Flrpic) (V2) and 90 wt .-% of the compound. 2 , 4-bis (phenoxy) -6- (3-methyldiphenylamino) -1, 3,5-triazine (4) evaporated to a thickness of 30 nm, the former compound acts as an emitter, the latter as a matrix material.

For the described OLED, the following electro-optical data result:

Claims

claims

1. Organic light-emitting diode containing at least one diphenylamino-bis (phenoxy) and / or bis (diphenylamino) -phenoxytriazine compound of the general formula (I)

in which mean:

CR, N or P, or - if n = 0 - additionally O or S;

D is CR, N or P or, if n = 0, additionally O or S;

CR, N or P, or - if n = 0 - additionally O or S;

G is CR, N or P or, if n = 0, additionally O or S;

L is CR ¹⁵ , N or P, or - if n = 0 - additionally O or S;

RI _D Z _D 3 _D 4 _D b _D b _D / nu n 9S _D [D10 are independently hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S -Aryl, halogen, pseudohalogen, amino or other donor or acceptor substituents;

R ¹¹ , R ¹² , R ¹³ , R ¹⁴ , R ¹⁵ independently of one another are hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, pseudohalogen, Amino, more Substituents with donor or acceptor action or a radical of the formula (i), (ii) or (iii) wherein the radicals and groups X ', R ^1' , R ^{2 '} , R ^3' , R ^{4 '} , R ^5' , R ^{6 '} , R ^7' , R ^{8 '} , R ^9' and R ^{10 '} in the rest of formula (i), which radicals and groups X ^'a, R ^1a, R ^2a, R ^3a, R ^4a, R ^5a, R ^6a, R ^7a, R ^8a, R ^9a and R ^1oa (in the radical of formula II ) and the radicals and groups X ' ^b , R ^rb , R ^2b , R ^3b , R ^4'b , R ^5b , R ^6b , R ^7b , R ^8b , R ^9b and R ^1Ob in the radical of the formula (iii) independently from each other with respect to the radicals and groups X, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ and R ^{10 have} mentioned meanings, and

the radicals R ³⁴ , R ³⁵ , R ³⁶ , R ³⁷ , R ³⁸ , R ³⁹ , R ⁴⁰ , R ^{34 '} R ^35' , R ^{36 '} R ³⁷ and R ^{38' are} independently hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, halogen, pseudohalogen, amino or other substituents with donor or acceptor action;

X

m

M is CR, N or P or, if m = 0, additionally O or S;

CR, N or P, or - if m = 0 - additionally O or S;

T is CR, N or P or, if m = 0, additionally O or S;

U is CR, N or P or, if m = 0, additionally O or S;

V is CR, N or P or, if m = 0, additionally O or S;

_D 16 _D 17 _D 18 _D 19 _D 20 _D 21 _D 22 _D 23 _D 24 _D 25 Ix, ΓΛ, ΓΛ, ΓΛ, ΓΛ, ΓΛ, ΓΛ, ΓΛ, ΓΛ, ΓΛ independently of one another hydrogen, alkyl, aryl, heteroaryl, OH , O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, halogen, pseudohalogen, amino or other substituents with donor or acceptor action; independently of one another are hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, pseudohalogen, amino, further substituents with donor or acceptor action; or a radical of the formulas (iv), (v) or (vi)

wherein the radicals and groups X ", R ^1" , R ^{2 "} , R ^3" , R ^{4 "} , R ^5" , R ^{6 "} , R ^7" , R ^{8 "} , R ^9" and R ¹⁰ in the rest of Formula (iv), radicals and groups X " ^a , R ^{1 a} , R ^{2" a} , R ^{3 "a} , R ^{4" a} , R ^{5 "a} , R ^{6" a} , R ^{7 "a} , R ^{8" a} , R ^{9 "a} and R ^{10" a} in the radical of the formula (V) and the radicals and groups X " ^b , R ^rb , R ^{2" b} , R ^{3 "b} , R ^{4" b} , R ^{5 "b} , R ^{6 "b} , R ^{7" b} , R ^{8 b} , R ^{9 b} and R ^{10 b} in the radical of formula (vi) independently of one another with respect to the radicals and groups X, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ and R ^{10 have} mentioned meanings, and

the radicals R ^{34 "} , R ^35" , R ^{36 "} , R ^37" , R ^{38 "} , R ^{39 '} R ^40' R ^34" , R ^{35 "'} R ^36"' R ^{37 "} and R ^{38" are} independently Hydrogen, alkyl, aryl, heteroaryl, OH, O-alkyl, O-aryl, O-heteroaryl, SH, S-alkyl, S-aryl, halogen, pseudohalogen, amino or other substituents with donor or acceptor action;

n, m are independently 0 or 1, preferably 1.

Organic light-emitting diode according to claim 1, characterized in that at least one of the radicals R ² , R ³ , R ⁴ , R ⁷ , R ⁸ , R ⁹ , R ¹² , R ¹³ , R ¹⁴ , and / or at least one of R ¹⁷ , R ¹⁸ , R ¹⁹ , R ²² , R ²³ , R ²⁴ or R ²⁷ , R ²⁸ , R ^{29 is} not hydrogen.

Organic light emitting diode according to claim 1 or 2, characterized in that the compound of formula (I) 1 to 10, preferably 1,

2,

3, 4, 5 or 6 radicals R ¹ to R ³⁰ , which are not hydrogen and all other radicals R ¹ to R ^{30 are} hydrogen.

4. Organic light-emitting diode according to one of claims 1 to 3, characterized in that the radicals R ¹ , R ⁵ , R ⁶ , R ¹⁰ , R ¹¹ , R ¹⁵ , R ¹⁶ , R ²⁰ , R ²¹ , R ²⁵ , R ²⁶ and R ^{30 is} hydrogen.

5. Organic light-emitting diode according to one of claims 1 to 4, characterized in that the radicals R ¹ to R ^{40 are} independently hydrogen, halogen-substituted alkyl, pseudohalogen, O-alkyl or O-aryl, preferably hydrogen, Cr to Cβ-alkyl , C ₁ -C ₆ -alkyl which is substituted by one or more F atoms, C 1 - to C ₆ -alkyl or OC ₆ -aryl, particularly preferably methyl, CF ₃ or O-methyl.

6. Organic light-emitting diode according to one of claims 1 to 5, characterized in that the compounds of formula (I) as matrix material and / or hole / Excitonenblockermaterial and / or electron / Excitonenblockermaterial and / or hole injection material and / or electron Injection material and / or hole conductor material and / or electron conductor material can be used.

7. Organic light-emitting diode according to claim 6, characterized in that the compounds of formula (I) are used as matrix materials in the light-emitting layer.

8. Organic light-emitting diode according to one of claims 1 to 7, characterized in that the compounds of formula (I) are used together with at least one triplet emitter in the organic light emitting diode.

9. Use of compounds of the formula (I) according to one of claims 1 to 5 in organic light-emitting diodes.

10. Light-emitting layer comprising at least one compound of the formula (I) according to one of claims 1 to 5, preferably together with at least one triplet emitter.

1. Blocking layer for electrons, block layer for holes, hole injection layer, electron-injection layer, hole conductor layer and / or electron conductor layer containing at least one compound of the formula (I) according to one of claims 1 to 5.

12. Organic light-emitting diode comprising at least one light-emitting layer according to claim 10 and / or at least one block layer for electrons, block layer for holes, hole-injection layer, electron-injection layer,

Hole conductor layer and / or electron conductor layer according to claim 11.

13. Device selected from the group consisting of stationary screens such as screens of computers, televisions, screens in printers, kitchen appliances and billboards, lighting, signboards and mobile screens such as screens in cell phones, laptops, digital cameras, vehicles and destination displays on buses and trains and lighting units containing at least one organic light-emitting diode according to one of claims 1 to 8 or 12.