EP1866978A1

EP1866978A1 - Use of compounds containing aromatic or heteroaromatic rings linked via carbonyl group-containing groups, for use as matrix materials in organic light-emitting diodes

Info

Publication number: EP1866978A1
Application number: EP06725284A
Authority: EP
Inventors: Klaus Kahle; Christian Dr. Lennartz; Oliver Dr. Molt; Simon Dr. Nord; Martina Dr. Egen; Wolfgang Prof. Dr. Kowalsky; Christian Schildknecht; Hans-Herrmann Dr. Johannes
Original assignee: BASF SE
Current assignee: BASF SE
Priority date: 2005-03-24
Filing date: 2006-03-23
Publication date: 2007-12-19
Also published as: CN101171697A; DE102005014284A1; WO2006100298A1; KR20070118656A; JP2008538858A

Abstract

The invention relates to the use of compounds that contain aromatic or heteroaromatic rings that are linked via carbonyl group-containing groups as matrix materials in organic light-emitting diodes. The invention also relates to a light-emitting layer that comprises at least one such compound as the matrix material and at least one additional substance distributed therein as the emitter or that consists of at least one such compound as the matrix material and at least one additional substance distributed therein as the emitter. Finally, the invention relates to an organic light-emitting diode comprising such a light-emitting layer and to a device comprising such an organic light-emitting diode.

Description

Use of compounds containing aromatic or heteroaromatic rings containing groups via carbonyl groups as matrix materials in organic light-emitting diodes

description

The present invention relates to the use of compounds containing aromatic or heteroaromatic rings connected via carbonyl groups containing groups, as matrix materials in organic light-emitting diodes. Furthermore, the present invention relates to a light-emitting layer which contains at least one such compound as a matrix material and at least one further substance distributed therein as an emitter or which consists of at least one such compounds as matrix material and at least one further substance distributed therein as an emitter, an organic light-emitting diode containing such a light-emitting layer, and a device containing such an organic light-emitting diode.

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 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.

Numerous substances have been proposed which emit light upon excitation by electric current. These can act as a light emitter per se or they consist of a matrix material which contains the actual light emitter in distributed form.

For example, US 2004/0209115 A1 discloses as matrix materials compounds of the general formula XAr ¹ Ar ² Ar ³ Ar ⁴ in which X represents carbon, silicon, germanium, tin, lead, titanium, zirconium or hafnium and the variables Ar ¹ to Ar ⁴ denote optionally substituted and optionally linked together phenyl or mononuclear heteroaryl radicals.

In the publication WO 00/70655 A2 4,4'-N, N'-dicarbazole-biphenyl ("CBP") is proposed as the matrix material.

M. Nomura et al. describe in the publication Synthetic Metals, 132 (2002),

9-13, the preparation of 1,1,1-tris (4- (4- (N-phenyl-1-naphthylamino) benzoyloxy) -phenyl) ethane and its use as hole transport material in organic light emitting barren. The suitability of this substance as a matrix material is not apparent from this work.

The object of the present application was therefore to provide further matrix materials for use in OLEDs, in particular for the light-emitting layers of the OLEDs, which are easily accessible and, in combination with the actual emitter (s), bring about good luminances and quantum yields in OLEDs.

This object is achieved by the use of compounds of general formula I.

as matrix materials in organic light-emitting diodes, the variables having the following meanings:

Ar ^{1 is} an aromatic or heteroaromatic five- or six-membered ring which is monosubstituted or disubstituted benzanelated with one or more halogen, NO ₂ , NO, CN, CHO, R ¹ , X ¹ -CO-R ¹ , X ¹ -SO ₂ - R ¹ , X ¹ -R ^{1 '} , CO-X ¹ -R ^1' or SO ₂ -X ¹ -R ¹ 'may be substituted,

Ar ^{2 is} an n-valent organic radical containing one or more aromatic and / or heteroaromatic five- or six-membered rings containing one or more halogen, NO ₂ , NO, CN, CHO, R ² , CO-R ² , X ² -SO ₂ -R ² , X ² -R ² 'or SO ₂ -X ² -R ^2' may be substituted,

E is -CO-O-, -O-CO-, -CO-S-, -S-CO-, -CO-NR ^'-, ^-NR' -CO-, -0-CO-O- or

the latter grouping over the two marked with asterisks

Positions at two adjacent carbon atoms of Ar ¹ or Ar ² and via the nitrogen atom to Ar ² or Ar ^1, respectively,

R ^{1 is} Ci-C ₂₀ -AlkVl, C ₂ -C ₂₀ alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -Cio-aryl-CrC _2O- alkyl, C ₆ -C _1o- aryl-C ₂ -C ₂ o-alkenyl, heteroaryl-C _r C ₂ o-alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the C ₁ -C ₂₀ - or C ₂ -C ₂₀ -carboxylic one or more non-adjacent CH ₂ groups can be replaced by oxygen atoms, -N (C ₁ -C ₂₀ alkyl) - and / or carbonyl groups and both the C ₆ -C ₁₀ -aryl and the heteroaryl with one or more Halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, XR ^' , CO-XR ^' or SO ₂ -XR ^' may be substituted,

R ² -C ₂₀ alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having from 2 to 12 carbon atoms, Ce-C ^ -aryl-CrCao-alkyl, C ₆ -C _{1 o} aryl C ₂ -C ₂ o-alkenyl, heteroaryl-C, -C ₂₀ alkyl, or heteroaryl-C ₂ -C ₂₀ alkenyl, each having 2 to 12 carbon atoms in the heteroaryl radical, wherein the Ci-C ₂₀ - or C ₂ -C ₂₀ -carbon chain one or more non-adjacent CH ₂ groups may be replaced by oxygen atoms, -N (C _r C ₂₀ alkyl) - and / or carbonyl groups and both the C ₆ -C _1o -aryl and the heteroaryl may also be substituted by one or more halogen, NO ₂ , NO, CN ₁ CHO, R, CO-R, X-SO ₂ -R, XR ^' or SO ₂ -XR ^' ,

R ¹ ', R ² ' are independently of one another hydrogen or independently of R ¹ or R ² the same meaning as R ¹ or R ² ,

R Ci-C ₂ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having from 2 to 12 carbon atoms, C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl, heteroarylCrC ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, has the same meaning as R,

X ¹ , X ² , X independently of one another oxygen, sulfur or NR ^{1 '} or NR ^2' or NR ^' , where in the event that X ¹ -R ^1' or X ² -R ^{2 '} or XR ^' corresponds to an N (R ^{1 '} ) ₂ - or N (R ^2' ) ₂ - or N (R ^' ) ₂ group, the two radicals R ^1' and R ² 'or R ^' together a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or

C ₄ - or C ₅ -alkadienylene bridge in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadienylenbrücke the interconnected by the double bond (s) carbon atoms part of a six-membered optionally benzanellierten aromatic or heteroaromatic ring,

and

n values of 1, 2, 3, 4, 5 or 6, with the proviso that the total number of aromatic and / or heteroaromatic five- or six-membered rings contained in Ar ^{2 is} at most six.

If E in formula I is -CO-O-, -O-CO-, -CO-S-, -S-CO-, -CO-NR ^' - or -NR'-CO-, its attachment to Ar ^{2 takes place} both via the carbonyl group and via the heteroatom. Furthermore, it is possible that in one and the same molecule of the formula I, a part of the n above-mentioned linking groups E via the carbonyl group, another part is attached via the heteroatoms.

Preferably, all n groups E are attached to Ar ² in the same way, ie either via the carbonyl group or via the heteroatom.

In general, the π groups E in formula I can be different from one another.

Preferably, the n groups E in formula I are the same and, if different bonds to Ar ^{2 are} possible, bound in the same way.

In general, the n radicals Ar ¹ in formula I can be different from one another.

Preferably, the n radicals Ar ¹ in formula I are the same.

In general, the n groupings Ar ¹ -E in formula I can be different from one another. In particular, here on the one hand, the linking groups E differ both in their chemical nature and, in the given case, in their nature of binding to Ar ² from each other, on the other hand, the radicals Ar ^{1 may} differ from each other in their chemical nature.

Preferably, the n groupings Ar ¹ -E in formula I are the same. This means that each of the same radicals Ar ^{1 are} attached to Ar ² in the same way via the linking groups E, provided that there are different possibilities of attachment in the latter groups.

For the variables R ¹ and R ² and R ^{1 '} and R ^2' are:

as C ₁ -C _2O -alkyl, in which C _r C ₂ o-carbon chain one or more non-adjacent CH ₂ groups may be replaced by oxygen atoms, for example methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, 2-methylpentyl, heptyl, hept-3-yl, octyl, 2-ethylhexyl, isooctyl, nonyl, isononyl, decyl, isodecyl, undecyl, dodecyl, tridecyl, 3,5,5,7-tetramethylnonyl, isotridecyl (the above designations isooctyl, isononyl, isodecyl and isotridecyl are trivial terms and are derived from the alcohols obtained by the oxo process - cf. Ullmanns Encyklopadie der technischen Chemie, 4th Edition, Volume 7, pages 215 to 217, and Volume 11, pages 435 and 436), tetradecyl, pentadecyl, hexadecyl, hepta- decyl, octadecyl, nonadecyl, eicosyl, methoxymethyl, 2-ethylhexoxymethyl, 2-methoxyethyl, 2-ethoxyethyl, 2-propoxyethyl, 2-isopropoxyethyl, 2-butoxyethyl, 2- or 3-methoxypropyl, 2- or 3-ethoxypropyl, 2- or 3-propoxypropyl, 2- or 3-butoxy propyl, 2- or 4-methoxybutyl, 2- or 4-ethoxybutyl, 2- or 4-propoxybutyl, 2- or 4-butoxybutyl, 3,6-dioxaheptyl, 3,6-dioxaoctyl, 4,8-dioxanonyl, 3, 7-dioxaoctyl, 3,7-dioanonone, 4,7-dioxaoctyl, 4,7-dioxanonyl, 4,8-dioxadecyl, 3,6,8-trioxadecyl, 3,6,9-trioza-undecyl, 3, 6,9,12-tetraoxatridecyl or 3,6,9,12-tetraoxatetradecyl; Corresponding radicals in which non-adjacent CH ₂ groups have been replaced by -N (C ₁ -C ₂ O-AIKyI) or carbonyl groups can be formally derived from the oxygen-containing radicals listed above by replacing the oxygen atoms with N (C ₁ -C ₂₀ -AikyI) - or carbonyl derived.

as C ₂ -C ₂₀ alkenyl in whose C ₂ -C ₂₀ carbon chain one or more non-adjacent CH ₂ groups may be replaced by oxygen atoms, N (C _r C ₂₀ alkyl) and / or carbonyl groups, in particular C ₂ -C ₂₀ -Alk-1-enyl radicals. These can be derived from suitable previously exemplified radicals by formal replacement of two hydrogen atoms, which are located on adjacent carbon atoms, by another carbon-carbon bond.

as C ₆ -C ₀ -A ^ lC ₁ -C ₂₀ alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ alkenyl, heteroaryl-C ₁ -C ₂₀ alkyl and heteroaryl-C ₂ -C ₂₀ alkenyl each having 2 to 12 carbon atoms in the heteroaryl radical, in which C ₁ -C ₂₀ - or C ₂ -C _2o carbon chain, one or more non-adjacent CH ₂ groups are replaced by oxygen atoms, N (C _r C ₂₀ alkyl) - and / or carbonyl groups may be replaced, in particular those radicals which can be derived from the previously exemplified radicals by formal replacement of a terminal hydrogen atom by C ₆ -C ₁₀ -aryl or heteroaryl having 2 to 12 carbon atoms;

as C ₆ -C ₁₀ -aryl, in particular phenyl and naphthyl;

as heteroaryl having 2 to 12 carbon atoms, such radicals which are derived, for example, from pyrrole, furan, thiophene, pyrazole, isoxazole, isothiazole, imidazole, 1H-1, 2,3-triazole, 1H-1, 2,4-triazole, Pyridine, pyrazine, pyridazine, 1H-azepine, 2H-azepine, oxazole, thiazole, 1, 2,3-, 1, 2,4- or 1, 3,4-oxadiazole, 1, 2,3-, 1, 2 , 4- or 1, 3,4-thiadiazole and optionally the benzo or dibenzoanellierten rings, such as quinoline, isoquinoline, indole, benzo [b] furan (coumarone), benzo [b] thiophene (thionaphthene), carbazole, Dibenzofuran, dibenzothiophene, 1H-indazole, indoxazole, benzo [d] isothiazole, anthranil, benzimidazole, benzoxazole, benzothiazole, cinnoline, phthalazine, quinazoline, quinoxaline or phenazine. In the case of the variables R ¹ and R ¹ 'and R ^2' , the C ₆ -C ₁₀ -aryl or heteroaryl having 2 to 12 carbon atoms with one or more substituents halogen, NO ₂ , NO, CN, CHO, R, X -CO-R, X-SO ₂ -R, XR ^' , CO-XR ^' or SO ₂ -XR ^' .

In the case of the variables R ² and R ^{2 '} , the C ₆ -C ₁₀ -aryl or heteroaryl having 2 to 12 carbon atoms with one or more substituents halogen, NO ₂ , NO, CN, CHO, R, CO-R, X -SO ₂ -R, XR ^' or SO ₂ -XR ^{' be} substituted.

Halogen in this case in each case denotes fluorine, chlorine, bromine or iodine, in particular fluorine or chlorine.

For the variables R and R ^' as C _r C ₂₀ alkyl, C ₂ -C ₂₀ alkylene I ₁ C ₆ -C _1o- aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C _{1 o} -aryl-C ₂ -C ₂₀ -alkenyl, heteroaryl-C _r C ₂₀ -alkyl and heteroaryl-C ₂ -C ₂₀ -alkenyl with in each case 2 to 12 carbon atoms in the heteroaryl radical such radicals in question , which have already been listed as examples.

The variables X ¹ , X ² and X are independently oxygen, sulfur or NR ¹ 'or NR ^2' or NR '. If X ¹ -R ^{1 '} or X ² -R ^2' or XR ^' corresponds to an N (R ¹ V or N (R ² ') ₂ - or N (R ^' ) ₂ group, the two R ^{1 '} or R ^2' or R ^' together form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge one or two non-adjacent CH ₂ groups may be replaced by carbonyl groups. Furthermore, in the case of the alkenylene and Alkadienylenbrücke the interconnected by the double bond (s) of carbon atoms be part of a six-membered, optionally benzo-fused aromatic or heteroaromatic ring.

For example, here as N (R ^{1 '} ) ₂ - or N (R ^2' ) ₂ - or N (R ^' ) ₂ groups, in which the two radicals R ^1' and R ^{2 '} or R ^' together form corresponding bridges

In a preferred embodiment, the present invention relates to the use of compounds of the formula I ₁ in which the variables have the following meanings: Ar ^{1 is} an aromatic or heteroaromatic five- or six-membered ring which is simply benzanellated and substituted with one or more halo, CN, R ¹ , X ¹ -CO-R ^1, -R ^{1 '} or CO-X ¹ -R ^1' can be,

Ar ^{2 is} an n-valent organic radical which contains one or more aromatic and / or heteroaromatic five- or six-membered rings which are substituted by one or more halogen, CN, R ² , CO-R ² or X ² -R ^{2 '} can,

E -CO-O-, -O-CO-, -CO-S-, -S-CO- or

wherein the latter group is attached to two adjacent carbon atoms of Ar ¹ and Ar ² via the two positions marked by asterisk and to Ar ² or Ar ¹ via the nitrogen atom,

R ^{1 is} C ₁ -C ₁₀ -alkyl, C ₂ -C ₁₀ -alkenyl, phenyl, heteroaryl of 3 to 5 carbon atoms, phenyl-C ₁ -C 4 -alkyl, phenyl-C ₂ -C ₁₀ -alkenyl, heteroaryl-C ₁ -C 4 -alkyl or heteroaryl-C ₂ -C ₁₀ alkenyl teroarylrest each having 3 to 5 carbon atoms in He, wherein in the C ₁ -C ₀ - or C ₂ -C _1o carbon chain, one or more non-adjacent CH ₂ groups are replaced by oxygen atoms , -N (C ₁ _{-C 10} -alkyl) and / or carbonyl groups and both the phenyl and the heteroaryl having one or more halogen, CN, R, X-CO-R, XR ^' or CO-XR ^' can be substituted,

R ² CrC-io-alkyl, C ₂ -C ₁₀ alkenyl, phenyl, heteroaryl having from 3 to 5 carbon atoms, phenyl-C _r C _1o alkyl, phenyl-C ₂ -C ₁₀ alkenyl, heteroaryl-C _r C ₁₀ -alkyl or heteroaryl-C ₂ -Cio-alkenyl teroarylrest each having 3 to 5 carbon atoms in He, wherein in the C ₁ -C ₁₀ - or C ₂ -C ₀ carbon chain, one or more non-adjacent CH ₂ groups are replaced by Oxygen atoms, -N (C ₁ -

C _1o alkyl) and / or carbonyl groups may be replaced and both the phenyl and the heteroaryl may be substituted by one or more halogen, CN, R, CO-R or XR ^' ,

R ^{1 '} , R ^{2' are} independently of one another hydrogen or independently of R ¹ or R ² the same meaning as R ¹ or R ² , R is C ₁ -C ₁₀ -alkyl, C ₂ -C ₁₀ alkenyl, phenyl, heteroaryl, alkyl having 3 to 5 carbon atoms, phenyl-CrC _10, phenyl-C ₂ -C ₁₀ alkenyl, heteroaryl-C _r C ₁₀ alkyl or heteroaryl-C ₂ -C ₁₀ -alkenyl having in each case 3 to 5 carbon atoms in the heteroaryl radical,

R 'is hydrogen or, independently of R, has the same meaning as R,

X ^{1 is} oxygen or NR ^{1 '} , where in the event that X ¹ -R ^1' corresponds to an N (R ^{1 '} ) ₂ group, the two radicals R ^1' together form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ alkenylene or C ₄ - or C ₅ -Alkadienylenbrücke in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny- lenbrücke by the double bond (e) interconnected carbon atoms may be part of a six-membered aromatic or heteroaromatic ring,

X ² , X are independently of one another oxygen or NR ^{2 '} or NR ^' , where in the event that X ² -R ^{2 '} or XR ^{' is} an N (R ^{2 '} ) ₂ - or N (R ^' ) ₂ - Group corresponds, the two radicals R ² 'and R ^' together may form a C ₄ - or C ₅ -alkylene or C ₄ - or C ₅ -alkenylene bridge, in which optionally one or two non-adjacent CH ₂ groups by carbonyl groups and in the case of the alkenylene bridge, the carbon atoms joined together by the double bond may be part of a six-membered aromatic or heteroaromatic ring,

and

n values of 1, 2, 3 or 4,

with the proviso that the total number of aromatic and / or heteroaromatic five- or six-membered rings contained in Ar ^{2 is} a maximum of four.

In a particularly preferred embodiment, the present invention relates to the use of compounds of the formula I in which the variables have the following meanings:

Ar ^{1 is} an aromatic or heteroaromatic five- or six-membered ring which may be substituted by one or more halogen, CN, R ¹ , X ¹ -CO-R ¹ , X ¹ -R ¹ 'or CO-X ¹ -R ^1' .

Ar ^{2 is} an n-valent organic radical containing one or more aromatic and / or heteroaromatic five- or six-membered rings, which with one or more halogen, CN, R ² , CO-R ² or X ² -R ^{2 '} may be substituted,

E -CO-O- or -O-CO-,

R ¹ , R ² independently of one another are C ₁ -C ₈ -alkyl, phenyl, heteroaryl having 3 to 5 carbon atoms, phenylCrCβ-alkyl, phenylC ₂ -C ₈ -alkenyl, heteroarylC _r C ₈ -alkyl or heteroaryl C ₂ -C ₈ -alkenyl having in each case 3 to 5 carbon atoms in the heteroaryl radical, where both the phenyl and the heteroaryl may be substituted by one or more halogen, CN, R or XR ^' ,

RC ₁ -C ₈ -alkyl or phenyl,

R 'is hydrogen or, independently of R, has the same meaning as R,

X ¹ oxygen or NR ^{1 '} , wherein in the event that X ¹ -R ^1' corresponds to an N (R ^{1 '} ) ₂ group, the two radicals R ¹ ' together a C ₄ - or C ₅ alkylene or

C ₄ - or C ₅ alkenylene bridge can form, in which optionally one or two non-adjacent CH ₂ groups may be replaced by carbonyl groups,

X ² , X are independently oxygen or NR ^{2 '} or NR ^' ,

and

n values of 1, 2, 3 or 4,

With respect to the total number of aromatic and / or heteroaromatic rings, the proviso is that the total number of aromatic and / or heteroaromatic five- or six-membered rings contained in Ar ^{2 is} at most six, or preferably or particularly preferably four, meaning that, for example, in Ar ² contained naphthyl, benzofuran, benzimidazole, benzoxazole or benzothiazole radicals as two rings, anthracene, carbazole or Dibenzofuranreste as three rings and triphenylene as four rings to be considered. This proviso is also to be understood as meaning that in the total number of aromatic and / or heteroaromatic rings, those rings are also to be taken into account which in the substituents R ² , CO-R ² , X ² -SO ₂ -R ² , X ² - R ^{2 '} and SO ₂ -X ² -R ^{2' of} the aromatic and / or heteroaromatic rings of the organic radical Ar ² can appear. For example, this is the case when R ² and R ² 'themselves C ₆ -C ₁₀ -ArVl, heteroaryl having 2 to 12 carbon atoms, C6-C ₁₀ aryl-C ₂ -C ₂₀ alkenyl, heteroaryl-C _r C ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ correspond alkenyl each having 2 to 12 carbon atoms in the heteroaryl. Furthermore, this is also the case when R ² and R ^{2 '} in the groupings CO-R ² , X ² -SO ₂ -R ² and X ² - R ^2' itself contain no aromatic or heteroaromatic rings, but these in the linking group X ² when the latter is NR ² (or NR ^{2 '} ) and R ² (or R ² ') C ₆ -C ₁₀ aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C _1o- aryl-CrC ₂ o-alkyl, C ₆ -C _1o -aryl-C ₂ -C ₂ o-alkenyl, heteroaryl-CrC ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl, each having 2 to 12 Carbon atoms in the heteroaryl corresponds.

Furthermore, possible substituents of the one or more aromatic and / or heteroaromatic five- or six-membered rings in the n-valent organic radical Ar ² are to be understood as meaning only radicals which are not part of two or more corresponding rings.

This is exemplified by the following compound to be used according to the invention

explained.

The fragment

For the purposes of the present invention, it corresponds to a divalent organic radical Ar ² (n = 2) which contains two six-membered aromatic rings. The latter are each substituted by two methyl radicals (corresponding to two substituents R ² in the meaning of a C ₁ -C _2O -AIKyI); the cyclopentylidene bridge between the two rings is not understood as a further substituent of the rings but as part of the organic radical Ar ² . For the purposes of the present invention, the two benzyloxy groups attached to the divalent radical Ar ² correspond to aryl groups Ar ¹ -E in which both Ar ¹ each have the meaning of a six-membered aromatic ring and both E have the meaning of a carbonyloxy group, which is attached via the carbonyl group to Ar ¹ and via the heteroatom oxygen to the organic radical Ar ² .

For the purposes of the present invention, of course, the attachment of one group Ar ¹ -E via oxygen and the other group Ar ¹ -E via the carbonyl group, or the connection of both aryl groups Ar ¹ -E via the carbonyl group the organic radical Ar ² possible.

In these cases, the compounds shown below are obtained

respectively

In addition, among possible substituents of the one or more aromatic and / or heteroaromatic five- or six-membered rings in the n-valent organic radical Ar ² are to be understood only those radicals which are attached only to a position of the corresponding ring. By way of example, this is the case of the compound shown below which is to be used according to the invention

executed. For the purposes of the present invention, the fragment corresponds

a divalent organic radical Ar ² which contains a six-membered aromatic ring and is not further substituted. The 1, 1, 4,4-tetramethyltetra- methylene bridge, which bridges the carbon atoms in the 2- and 3-position of the same ring, is understood as part of the organic radical Ar ² .

Exemplary are in the compound listed below

even both of the above aspects are reproduced.

This is how the fragment corresponds in the context of the present invention, a divalent organic radical Ar ² which contains two six-membered aromatic rings which are each substituted by two methyl radicals.

The previous statements as well as exemplary explanations are to be applied correspondingly to all compounds included in the present application.

In particular, according to the invention, those compounds and their preferred embodiments are used which have a molecular weight of 200 to 2000 g / mol.

The compounds of the formula I used according to the invention can be prepared by processes known to the person skilled in the art and are outstandingly suitable for use as matrix materials in organic light-emitting diodes (OLEDs).

In the following, various groups of compounds to be used according to the invention are described, in which the organic radicals Ar ² are defined in more detail.

Since the introduction of different variables for each of the groups described would lead to an unmanageable variety of variable names, these are used repeatedly in the following. However, since the variables are defined locally for a group of connections, there is no danger of confusion.

A suitable group of compounds having divalent organic radicals Ar ² corresponds to the general formula 1

wherein the rings A ¹ and A ² independently of one another additionally by one or two C _r C ₄ alkyl or CiC ₄ -alkoxy and denote variables:

Y single chemical bond, C ₂ -C ₁₀ alkylene, oxygen, sulfur, SO, SO ₂ ,

NZ ¹ , -C (Z ² ) = C (Z ³ ) - or CZ ² Z ³ ,

Y ^' single chemical bond, oxygen or sulfur,

p is a value 0 or 1,

Z ^1, Z ^2, Z ³ are independently hydrogen, C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ - aryl, heteroaryl having from 2 to 12 carbon atoms, C ₆ -C ₀ -aryl -C ₁ -C ₂ Q-alkyl, C ₆ -C _1o aryl-C ₂ -C ₂₀ alkenyl, heteroaryl-Ci-C ₂₀ alkyl or heteroaryl-C ₂ -C ₂₀ - alkenyl each having 2 to 12 carbon atoms in the heteroaryl radical, where in the C ₁ -C ₂₀ or C ₂ -C ₂₀ -carbon chain one or more non-adjacent CH ₂ groups may be replaced by oxygen atoms, NCCrC ^ -alkyl) and / or carbonyl groups and both the C ₆ -C ₁₀ -aryl and the heteroaryl be substituted by one or more halogen, NO ₂ , NO, CN, CHO, Z, CO-Z, W-SO ₂ -Z, WZ 'or SO ₂ -WZ ^' can, being in the

Group -C (Z ² ) = C (Z ³ ) - or CZ ² Z ³ the two radicals Z ² and Z ³ together a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ or C ₅ -alkadienylene bridge in which optionally one or two non-adjacent CH ₂ groups are replaced by oxygen atoms and / or carbonyl groups and in the case of the alkenylene and alkadienylene bridges which are linked together by the double bond (s) Carbon atoms may be part of a six-membered optionally benzo-fused aromatic or heteroaromatic ring,

Z is C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having from 2 to 12 carbon atoms, C ₆ -C ₁₀ aryl-CrC ₂₀ alkyl, C ₆ -C _1o - Aryl-C ₂ -C ₂₀ -alkenyl, heteroarylCrC ^ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

Z ^'is hydrogen or, independently of Z, has the same meaning as Z,

W oxygen, sulfur or NZ ^' , where in the event that WZ' of an N (Z ^' ) ₂ -

Group corresponds, the two radicals Z ^' together can form a C ₄ - or C ₅ -alkenyl, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -Alkadienylenbrücke in which optionally one or two not adjacent

CH ₂ groups may be replaced by carbonyl groups, and in the case of alkenylene and Alkadienylenbrücke the comparable with each other by the double bond (s) bonded carbon atoms may be part of a six-membered, optionally benzo-fused aromatic or heteroaromatic ring,

Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which is benzanellated once or twice and is substituted by one or more halogen, NO ₂ , NO, CN, CHO, R ¹ , X ¹ -CO-R ¹ , X ¹ -SO ₂ -R ¹ , X ¹ -R ^{1 '} , CO-X ¹ -R ^1' or SO ₂ -X ¹ -R ^{1 '} may be substituted,

E independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO-, -CO-NR ^' -, -

NR ^'is -CO-, -O-CO-O- or

R ^{1 is} C ₁ -C ₂₀ -alkyl C ₁ ₂ -C ₂₀ alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having from 2 to 12 carbon atoms, C ₆ -C _1o aryl-CrC ₂ O-alkyl, C ₆ - C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl, heteroaryl-C ₁ -C 4 -alkyl or heteroaryl C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the C ₁ -C ₂₀ - or C ₂ -C ₂₀ -carbon chain one or more non-adjacent CH ₂ groups may be replaced by oxygen atoms, N (C ₁ -C ₂₀ -alkyl) and / or carbonyl groups and both the C ₆ -C ₁₀ - Aryl and the heteroaryl be substituted with one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, XR ^' , CO-XR' or SO ₂ -XR ^' can

R ^{1 'is} hydrogen or, independently of R ^1, the same meaning as R ¹ ,

, Atoms RC _r C ₂₀ alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having from 2 to 12 carbon, C6-C ₁₀ aryl-CrC ₂₀ alkyl, C ₆ -C ₁₀ - Aryl-C ₂ -C ₂₀ -alkenyl, heteroarylC _r C ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, the same meaning as R

and X ¹ , X independently of one another oxygen, sulfur or NR ^{1 '} or NR ^' , where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups are replaced by carbonyl groups and in the case of the alkenylene and alkadienylene bridges the carbon atoms joined together by the double bond (s) may be part of a six-membered, optionally benzanellated, aromatic or heteroaromatic ring,

with the proviso that in the radicals Z ¹ , Z ² and Z ³ carbon-bonded hydrogen atoms may be partially or completely replaced by fluorine atoms.

With regard to the definition of the variables Z ¹ , Z ² and Z ³ or Z and Z ^' or W, it is analogous to those already mentioned above for the variables R ^1' and R ^{2 '} or R and R ^' or X ¹ , X ² and X are given given definitions and radicals listed by way of example; With regard to the remaining variables Ar ¹ , R ¹ , R ^{1 '} , R, R ^' , X ¹ and X and their preferences, reference is likewise made to the definitions given above and the radicals listed by way of example.

A particularly useful group of compounds corresponding to the general formula 1, wherein rings A ¹ and A ² in addition with one or two Ci-C ₄ alkyl or C ₁ -C ₄ -alkoxy may be substituted independently of one another have in each case and denote the variables

Y is a single chemical bond, C ₂ -C ₄ -alkylene, SO ₂ or CZ ² Z ³ ,

Y ^' single chemical bond or oxygen,

p is a value 0 or 1,

Z ² , Z ³ independently of one another C ₁ -C ₁₀ -alkyl or C ₆ -C ₁₀ -aryl, where the

C ₆ -C ₁₀ -ArVl with one or more halogen, in particular fluorine, Z, CO-Z or OZ ^' may be substituted and in the group CZ ² Z ^3, the two radicals Z ² and Z ³ together a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenyl- or C ₄ - or C ₅ -Alkadienylenbrücke can form in which one or two non-adjacent CH ₂ groups replaced by oxygen atoms and / or carbonyl groups and in the case of Alkenylene and alkadienylene bridges, the carbon atoms interconnected by the double bond (s) may be part of a six-membered, optionally benzo-fused, aromatic or heteroaromatic ring, ZC ₁ -C ₁₀ -alkyl or C ₆ -C ₁₀ -aryl,

Z 'is hydrogen or, independently of Z, has the same meaning as Z,

Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring substituted with one or more halogen, in particular fluorine, R ¹ , X ¹ -CO-R \ X ¹ -R ^{1 '} or CO-X ¹ -R ^1' substituted can be,

E is independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-,

R ^{1 is} independently C ₁ -C ₀ -alkyl, C ₂ -C ₁₀ alkenyl, C ₆ -C _1o aryl, C ₆ -C ₁₀ -

Aryl-Ci-Ci _θ -alkyl or C ₆ -C ₁₀ -aryl-C ₂ -C ₁₀ -alkenyl _l wherein in the C ₁ -C ₁₀ - or C ₂ -C _1o carbon chain one or more non-adjacent CH ₂ groups are replaced by oxygen atoms, N (C _r C _1o alkyl) - and / or carbonyl groups can be replaced and the C ₆ -C ₁₀ aryl with one or more halogen, R,

X-CO-R, XR 'or CO-XR ^' may be substituted,

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

RC ₁ -C ₁₀ alkyl or C ₆ -C ₁₀ aryl,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen or NR ^{1 '} or NR ^' , where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ - Group corresponds, the two radicals R ¹ 'and R ^' together can form a C ₄ - or C ₅ -alkylene, C ₄ - o of the C ₅ alkenylene or C ₄ - or C ₅ -Alkadienylenbrücke, in which optionally one or two non-adjacent CH ₂ groups are replaced by carbonyl groups and in the case of the alkenylene and alkadienylene bridges the carbon atoms joined together by the double bond (s) may be part of a six-membered, optionally benzanellated, aromatic or heteroaromatic ring,

In the above-mentioned particularly suitable group of compounds of formula 1 are those of interest, wherein the rings A ¹ and A ² are each independently additionally substituted with one or two C _r C ₄ alkyl or C ₁ -C ₄ alkoxy can and do mean the variables OTT

a value 0,

^■ 2 ₇ 3

Z ^8, Z independently of one another C ₁ -C ₀ -alkyl or C ₆ -C ₁₀ aryl, wherein said C ₁ -C ₁₀ - alkyl having one or more fluorine and the C ₆ -C ₀ aryl with one or more fluorine , C ₁ -C ₀ -alkyl or C ₁ -C ₁₀ -alkoxy may be substituted and in the group Z ² CZ ^3, the two radicals Z ² and Z ³ together form a C ₄ - or C ₅ alkylene, C ₄ - or C ₅ alkenylene or C ₄ - or C ₅ alkadienylene bridge in which one or two non-adjacent CH ₂ groups replaced by oxygen atoms and / or carbonyl groups and in the case of alkenylene and Alkadienylenbrücke by the double bond (s ) carbon atoms connected to each other may form part of a six-membered, optionally benzanellated, aromatic or heteroaromatic ring,

and the remaining variables have the meaning given in the above-mentioned particularly suitable group of compounds of formula 1.

Examples of such compounds are:

22

In the above-mentioned particularly suitable group of compounds of formula 1 are further of interest in which the rings A ¹ and A ² are each independently additionally substituted in each case with one or two C 1 -C ₄ -alkyl or C 1 -C ₄ -alkoxy can and do mean the variables

Y ^'is a single chemical bond or oxygen,

P is a value 1,

Z ² , Z ³ independently of one another C _r C ₁₀ alkyl or C ₆ -C ₁₀ -ArVl, wherein the C ₁ -C ₁₀ - alkyl having one or more fluorine and the C ₆ -C _1o -aryl having one or more fluorine , Ci-Ci _θ- alkyl or C ₁ -C ₁₀ -alkoxy may be substituted and in the group CZ ² Z ^3, the two radicals Z ² and Z ³ together a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ alkenylene or C ₄ - or C ₅ alkadienylene bridge in which one or two non-adjacent CH ₂ groups replaced by oxygen atoms and / or carbonyl groups and in the case of alkenylene and Alkadienylenbrücke by the double bond (s) carbon atoms joined together may be part of a six-membered, optionally benzo-fused aromatic or heteroaromatic ring,

Examples of such compounds are

In the above-mentioned particularly suitable group of compounds of formula 1 are further of interest in which the rings A ¹ and A ² independently of one another additionally each with one or two C ₁ -C ₄ -AlkVl or C _r C ₄ alkoxy substituted can be and the variables mean

Y is a single chemical bond, C ₂ -C ₄ -alkylene, in particular ethylene, or SO ₂

Examples of such compounds are

Another suitable group of compounds having divalent organic radicals Ar ² corresponds to the general formula 2

(2)

wherein the rings A ¹ and A ² in addition may be substituted with one or two C _r C ₄ alkyl or C ₁ -C ₄ -alkoxy in each case independently of each other yet and denote variables:

Y divalent C ₆ -C ₀ aryl or divalent heteroaryl having 2 to 12 carbon atoms, wherein each of the C ₆ -C ₁₀ aryl and the heteroaryl having one or more halogen, NO _2, NO, CN, CHO, Z, CO -Z, W-SO ₂ -Z, WZ 'or SO ₂ -WZ ^' may be substituted,

C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, Ce-C ₁ -C aryl-C ₁ -C 4 -alkyl, C ₆ -C ₁₀ -aryl -C ₂ -C ₂₀ alkenyl, hetero aryl-C _r C ₂ o-alkyl or heteroaryl C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

Z ^'is hydrogen or, independently of Z, has the same meaning as Z,

W oxygen, sulfur or NZ ^' , where in the event that WZ ^{' of} an N (Z ^' ) ₂ -

Group corresponds, the two radicals Z 'together can form a C ₄ - or C ₅ -alkenyl, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -Alkadienylenbrücke in which optionally one or two not replacing adjacent CH ₂ groups by carbonyl groups and, in the case of the alkenylene and alkadienylene bridges, the carbon atoms interconnected by the double bond (s) may be part of a six-membered, if appropriate benzanelated, aromatic or heteroaromatic ring,

E independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO-, -CO-NR ^' -, -

NR'-CO-, -O-CO-O- or

R ^{1 is} C ₁ -C ₂₀ alkyl, C ₂ -C ₂₀ alkenyl, C ₆ -C _1o aryl, heteroaryl of 2 to 12 carbon atoms, C ₆ -C ₁₀ arylCyc ₂₀ alkyl, C ₆ -C _1o aryl-C ₂ -C _2O alkenyl, heteroaryl-Ci-C ₂₀ alkyl or heteroaryl-C ₂ -C ₂₀ alkenyl each having 2 to 12 carbon atoms in the heteroaryl, wherein the C ₁ -C ₂₀ - or C ₂ -C ₂₀ -carbon chain one or more non-adjacent CH ₂ groups may be replaced by oxygen atoms, N (C ₁ -C ₂₀ -alkyl) and / or carbonyl groups and both the C ₆ -C ₁₀ - Aryl and the heteroaryl having one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, X-R ', CO-XR ^' or SO ₂ - XR ^' may be substituted, R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

R is C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ aryl, heteroaryl atoms with 2 to 12 carbon, C ₆ -C _{1 o} aryl-C _r C ₂ o alkyl, C ₆ -C _{1 o} aryl-C ₂ -C _2O -aIkenyl, heteroaryl CrCao-alkyl or heteroaryl-C ₂ -C ₂₀ -aIkenyl each having 2 to 12 carbon atoms in the heteroaryl radical,

R 'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ^{1 '} or NR ^' , where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

With regard to the definition of the variables Z and Z ^' or W, reference is made mutatis mutandis to the definitions given above for the variables R and R ^' or X ¹ , X ² and X and examples listed by way of example; With regard to the remaining variables Ar ¹ , R ¹ , R ^{1 '} , R, R ^' , X ¹ and X and their preferences, reference is likewise made to the definitions already given above and the examples listed by way of example.

A particularly useful group of compounds represented by the general formula 2 wherein the rings A ¹ and A ² in addition with one or two -C ₄ alkyl or C ₁ -C ₄ -alkoxy may be substituted independently of one another have in each case and denote the variables

Y is bivalent phenyl or divalent heteroaryl having 2 to 5 carbon atoms, in which the phenyl may be substituted by one or more fluorine, CN, Z, -CO-Z or WZ ^' ,

Z is C 1 -C 4 -alkyl or phenyl,

Z ^'is hydrogen or, independently of Z, has the same meaning as Z,

W oxygen, sulfur or NZ ^' , where in the event that WZ ^{' of} an N (Z ') ₂ -

Group corresponds, the two radicals Z ^' together a C ₄ - or C ₅ - Alkylene, C ₄ - or C ₅ alkenylene or C ₄ - or C ₅ -Alkadienylenbrücke can form, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadienylenbrücke by the Double bond (s) may be part of a six-membered, optionally benzo-fused aromatic or heteroaromatic ring,

Ar ¹ independently of one another an aromatic or heteroaromatic five- or six-membered ring, which with one or more fluorine, R ¹ , X ¹ -CO-

R ¹ , X ¹ -R ¹ 'or CO-X ¹ -R ^1' may be substituted,

E is independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-,

R ¹ is C _r C ₁₀ -alkyl or phenyl, where the phenyl may be substituted with one or more fluorine, R, X-CO-R, XR ^'or ^CO-XR'

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

R is C 1 -C 4 -alkyl or phenyl,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ^{1 '} or NR ^' , where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R') ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups substituted by carbonyl groups and in the case of alkenylene and Alkadienylenbrücke the interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellierten aromatic or heteroaromatic ring.

As a divalent C ₆ -C ₀ aryl is 1,4-phenylene and 2,6-naphthyl, in particular 1, 4-phenylene in question.

Suitable divalent heteroaryl having 2 to 12 carbon atoms are radicals which are derived, for example, from pyrrole, furan, thiophene, pyrazole, isoxazole, isothiazole, imidazole, 1H-1, 2,3-triazole, 1H-1, 2, 4-triazole, pyridine, pyrazine, pyridazine, 1 H-azepine, 2H-azepine, oxazole, thiazole, 1, 2,3-, 1, 2,4- or 1, 3,4-oxadiazole, 1, 2,3 -, 1, 2,4 - or 1, 3,4-thiadiazole and optionally the benzo or dibenzoanellierten rings, such as quinoline, isoquinoline, indole, benzo [b] furan (coumarone), benzo [b] thiophene (thiomonaphthene), carbazole, dibenzofuran, dibenzothiophene, 1 H-indazole, indoxazole, benzo [d] isothiazole, anthranil, benzimidazole, benzoxazole, benzothiazole, cinnoline, phthalazine, quinazoline, quinoxaline or phenazine.

Suitable divalent heteroaryl having 2 to 5 carbon atoms are, in particular, radicals which are present, for example. Derive pyrrole, furan, thiophene, pyrazole, isoxazole, isothiazole, imidazole, 1H-1,2,3-triazole, 1H-1,2,4-triazole, pyridine, pyrazine, pyridazine, 1H-azepine, 2H-azepine, Oxazole, thiazole, 1, 2,3-, 1, 2,4- or 1, 3,4-oxadiazole, 1, 2,3-, 1, 2,4- or 1,3,4-thiadiazole.

Examples of such compounds are

Another suitable group of compounds having divalent organic radicals Ar ² corresponds to the general formula 3

(3)

wherein the rings A ¹ and A ² independently of one another have in each case with one or two C _r C ₄ alkyl or C ₁ -C ₄ -alkoxy may be substituted additionally,

each independently of one another represents a C ₂ -C ₃ -alkylene or C ₂ -C ₃ -alkenylene bridge which is optionally substituted by one or two C ₁ -C ₄ -alkyl groups and in which in the case of C ₂ -C ₃ -alkylene or C ₂ -C ₃ -alkylene; ₃ alkenylene bridge optionally a CH ₂ group replaced by oxygen or a carbonyl group and / or in the case of C ₂ -C ₃ -Alkeny- lenbrücke the carbon atoms interconnected by the double bond may be part of a six-membered optionally benzanellierten aromatic or heteroaromatic ring and the other variables mean:

independently of one another -CO-O-, -O-C0-, -CO-S-, -S-CO-, -CO-NR ^' -, -NR ^' -CO-, -O-CO-O- or wherein the latter group is attached to two adjacent carbon atoms of Ar ¹ and Ar ² via the two positions marked by asterisk and to Ar ² or Ar ¹ via the nitrogen atom,

R ^{1 is} C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ -aryl-C ₁ -C ₂ 0-alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl, heteroaryl-C ₁ -C ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the C ₂₀ - or C ₂ -C ₂₀ -Kohlen- chain one or more non-adjacent CH ₂ groups may be replaced by oxygen atoms, N (C _r C ₂₀ alkyl) and / or carbonyl groups and both the C ₆ -Ci ₀ -aryl and the heteroaryl having one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, XR ^' , CO-XR ^' or SO ₂ -XR ^' may be substituted

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

R is C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl, heteroaryl-C ₁ -C ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ^{1 '} or NR ^' , where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring. With regard to the definition of the variables Ar ¹ , R ¹ , R ^{1 '} , R, R ^' , X ¹ and X and their preferences, reference is made to the definitions given above and the radicals listed by way of example.

A particularly useful group of compounds represented by the general formula 3, wherein rings A ¹ and A ² independently of one another additionally by one or two Ci-C ₄ alkyl or C ₁ -C ₄ -alkoxy may be substituted in each case,

for the same optionally substituted with one or two C _r C ₄ -alkyl-substituted C ₂ -C ₃ -Al- kylen- or C ₂ -C ₃ -Alkenylenbrücken stand, in which optionally one

CH ₂ group replaced by oxygen or a carbonyl group and / or in the case of C ₂ -C ₃ alkenylene bridges, the carbon atoms connected by the double bond may be part of a six-membered aromatic or heteroaromatic ring and the other variables mean:

Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which may be substituted by one or more fluoro, R ¹ , X ¹ -CO-R ¹ , X ¹ -R ^{1 '} or CO-X ¹ -R ^1' .

E is independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-,

R ^{1 is} C ¹ -C 6 -alkyl or phenyl, where the phenyl may be substituted by one or more fluorine, R, X-CO-R, XR ^' or CO-XR ^' ,

R ^{1 'is} hydrogen or, independently of R ^1, the same meaning as R ¹ ,

R is cyanoalkyl or phenyl,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR', where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ group corresponds to the two radicals R ^{1 '} or R ^' together a C ₄ - or C ₅ -alkylene,

C ₄ - or C ₅ alkenylene or C ₄ - or C ₅ -Alkadienylenbrücke in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny- lenbrücke by the double bond (a) interconnected coal may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

Examples of such compounds are

A suitable group of compounds having trivalent organic radicals Ar ² corresponds to the general formula 4

(4)

wherein the rings A ^1, A ² and A ³ independently of one another may be substituted with one or two Ci-C ₄ alkyl or C ₁ -C ₄ -alkoxy and additionally each represent the remaining variables:

Z ^{1 is} hydrogen, C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ -aryl-C ₂ -C ₂ o-alkenyl, Heteroaryl-CrC ₂ o-alkyl or heteroaryl-C ₂ -C ₂ o-alkenyl each having 2 to 12 carbon atoms in the heteroaryl radical, wherein in the C ₁ -C ₂ O or C ₂ -C ₂₀ - carbon chain one or more not adjacent CH ₂ groups may be replaced by oxygen atoms, N (C ₁ -C ₂₀ -AIRyI) and / or carbonyl groups, and both the C ₆ -C ₁₀ -aryl and the heteroaryl may be replaced by one or more halogen, NO ₂ , NO , CN, CHO, Z, CO-Z, W-SO ₂ -Z, WZ ^' or SO ₂ -WZ ^' may be substituted,

ZC ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ -aryl-C ₁ -C ₂₀ -alkyl, C ₆ C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl, heteroaryl-C ₁ -C 6 -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

Z ^'is hydrogen or, independently of Z, has the same meaning as Z,

W oxygen, sulfur or NZ ', where in the event that WZ' of an N (Z ^' ) ₂ -

Group corresponds, the two radicals Z ^' together can form a C ₄ - or C ₅ -alkenyl, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -Alkadienylenbrücke in which optionally one or two not replacing adjacent CH ₂ groups by carbonyl groups and, in the case of the alkenylene and alkadienylene bridges, the carbon atoms interconnected by the double bond (s) may be part of a six-membered, if appropriate benzanelated, aromatic or heteroaromatic ring,

E independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO-, -CO-NR ^' -, -

NR ^'is -CO-, -O-CO-O- or

wherein the latter group is attached via the two starred positions to two adjacent carbon atoms of Ar ¹ or Ar ² and via the nitrogen atom to Ar ² or Ar ¹ , R ¹ C _r C ₂ o-alkyl, C ₂ -C ₂ o-alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁ o-aryl-C ₁ -C ₂ o- alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl, heteroaryl-CrC ₂ o-alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the C _One or more non-adjacent CH ₂ groups can be replaced by oxygen atoms, N (C ₁ -C ₂₀ -alkyl) and / or carbonyl groups and both the C ₁ -C ₂₀ - or C ₂ -C ₂₀ -carbon chain ₆ -C ₁₀ -aryl and the heteroaryl having one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, XR ^' , CO-XR ^' or SO ₂ -XR ^' may be substituted,

R ^{1 'is} hydrogen or, independently of R ^1, the same meaning as R ¹ ,

RC _r C ₂₀ alkyl, C ₂ -C ₂₀ alkenyl, C ₆ -C ₁₀ -alkyl, heteroaryl having 2 to 12 carbon atoms, Ce-C 1 -C aryl-C ₁ -C ₄ -alkyl, C ₆ -C ₁₀ -aryl C ₂ -C ₂₀ -alkenyl, heteroarylC _r C ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR', where in the event that X ¹ -R ¹ 'or XR' of an N (R ¹ ') ₂ - or N (R') ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

With regard to the definition of the variables Ar ¹ , R ¹ , R ^{1 '} , R, R ^' , X ¹ and X and their preferences, reference is made to the definitions given above and the radicals listed by way of example.

A particularly useful group of compounds represented by the general formula 4, wherein the rings A ^1, A ² and A ³ independently of one another additionally by one or two CiC ₄ alkyl or C ₁ -C ₄ -alkoxy may be substituted in each case and the other Variables mean: Z ¹ is hydrogen or Ci-C ₁₀ alkyl, wherein the Ci-Cio carbon chain, one or more non-adjacent CH ₂ groups are replaced by oxygen atoms, N (C ₁ -C ₀ -alkyl) - / or carbonyl groups and may be replaced,

Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which is benzanellated once or twice and which contains one or more halogen, CN, R ¹ , X ¹ -CO-R ¹ , X ¹ -R ^{1 '} or CO-X ¹ R ^{1 '} may be substituted,

E is independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-,

R ^{1 is} C ₁ -C _{1 (r is} alkyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 5 carbon atoms,

Ce-C 1-4 -aryl-C ₁ -C ₁₂ -alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₁₀ -alkenyl, heteroarylC _r C ₁₀ -alkyl or heteroaryl-C ₂ -C 10 -alkenyl, each having 2 to 5 carbon atoms teroarylrest in He, wherein in the C ₁ -C ₁₀ - or C ₂ -C ₀ carbon chain, one or more non-adjacent CH ₂ groups are replaced by oxygen atoms, N (CrCio-alkyl) - and / or carbonyl groups can be replaced and both the C ₆ -C ₀ aryl and the heteroaryl may be substituted with one or more halogen, CN, R, X-CO-R, XR ^'or ^CO-XR'

R ^{1 'is} hydrogen or, independently of R ^1, the same meaning as R ¹ ,

RC ₁ -C ₁₀ -AlkVl, C ₆ -C ₁₀ aryl, heteroaryl having 2 to 5 carbon atoms,

Ce-Cu-aryl-CrC ^ alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₁₀ alkenyl, heteroaryl-CrC ₁₀ alkyl or HeIeTOaIyI-C ₂ -C ₁₀ alkenyl each having 2 to 5 carbon atoms in the Hertoaryl rest,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ^{1 '} or NR', where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring. Examples of such compounds are

Another suitable group of compounds having trivalent organic radicals Ar ² corresponds to the general formula 5

(5)

in which the ring A ^{1 may} additionally be substituted by one to three C ₁ -C ₄ -alkyl or C ₁ -C ₄ -alkoxy and the other variables mean:

E independently of one another -CO-O-, -O-C0-, -CO-S-, -S-CO-, -CO-NR ^' -, -

NR ^'is -CO-, -O-CO-O- or

R ^{1 is} C ₁ -C ₂₀ -alkyl, C ₂ -C ₂ o-alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ -aryl-C ₁ -C ₂ 0-alkyl , C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl, heteroaryl-dC ^ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the CrC ₂₀ - or C ₂ -C ₂₀ carbon chain -Kohlen- one or more non-adjacent CH ₂ groups are replaced by oxygen atoms, N ₍₂₀ -alkyl) - and / or carbonyl groups can be replaced, and both the C ₆ -C ₁₀ aryl as well as the heteroaryl with one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, XR ^' , CO-XR ^' or SO ₂ -XR 'may be substituted .

R ^{1 'is} hydrogen or, independently of R ^1, the same meaning as R ¹ ,

RC _r C ₂₀ alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having from 2 to 12 carbon atoms, C ₆ -C ₀ aryl-Ci-C ₂₀ alkyl, C ₆ -C ₁₀ -Aryl-C ₂ -C ₂₀ -alkenyl, heteroarylC _r C ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, the same meaning as R

and

With regard to the definition of the variables Ar ¹ , R ¹ , R ^{1 '} , R, R', X ¹ and X and their preferences, reference is made to the definitions given above and the radicals listed by way of example.

In the event that the grouping via the two positions marked with asteris attached to two adjacent carbon atoms of Ar ² and via the nitrogen atom to Ar ¹ , there are no further substituents on the aromatic ring A ¹ apart from the three corresponding groupings Ar ¹ -E.

A particularly suitable group of compounds corresponds to the general formula 5, wherein the ring A ^{1 is} not further substituted except with the three aryl groups Ar ¹ -E and the other variables mean:

E is independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-,

R ^{1 is} C ₁ -C ₁₀ -alkyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 5 carbon atoms, C ₆ -C ₁ o-aryl-C ₂ -C ₁ o-alkenyl, heteroaryl-C ₁ -C ₁₀ -alkyl or heteroaryl-C ₂ -C ₁₀ -alkenyl having in each case 2 to 5 carbon atoms in the heteroaryl radical, where in the C ₁ -C ₁₀ - or C ₂ -Ci ₀ carbon chain one or more non-adjacent CH ₂ groups may be replaced by oxygen atoms, N (C ₁ -C ₁₀ alkyl) - and / or carbonyl groups and both the C ₆ -C _1o- aryl as well as the heteroaryl _{may be} substituted by one or more halogen, CN, R, X-CO-R, XR ^' or CO-XR ^' ,

R ^{1 'is} hydrogen or, independently of R ^1, the same meaning as R ¹ ,

R is C ₁ -C ₁₀ -alkyl, C ₆ -C ₁₀ aryl, heteroaryl having from 2 to 5 carbon atoms, C6-C ₁₀ aryl-C _r C ₁₀ alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₀ -alkenyl, heteroaryl-C _r C ₁₀ -alkyl or heteroaryl-C ₂ -C ₁₀ -alkenyl having in each case 2 to 5 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, the same meaning as R

and X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR', where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ¹ ') ₂ - or N (R') ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

Examples of such compounds are

A suitable group of compounds having tetravalent organic radicals Ar ² corresponds to the general formula 6

(6)

wherein the rings A ¹ and A ² additionally by one or two C ₁ -C ₄ or C -AIRyI independently | -C ₄ -alkoxy and denote variables:

Y single chemical bond, C ₂ -C ₁₀ -alkylene, oxygen, sulfur, SO, SO ₂ , NZ ¹ , -C (Z ² ) = C (Z ³ ) - or CZ ² Z ³ ,

Z, Z ¹ , Z independently of one another are hydrogen, C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ alkenyl, heteroaryl-Ci-C ₂₀ alkyl or heteroaryl-C ₂ -C ₂₀ alkenyl each having 2 to 12 carbon atoms in the Heteroaryl radical, wherein in the C ₁ -C ₂ O or C ₂ -C ₂ o carbon chain one or more non-adjacent CH ₂ groups replaced by oxygen atoms, N (C ₁ -C ₂₀ alkyl) - and / or carbonyl groups and both the C ₆ -C ₁₀ -aryl and the heteroaryl with one or more halogen, NO ₂ , NO, CN, CHO, Z, CO-Z, W-SO ₂ -Z, WZ ^' or SO ₂ - WZ ^' may be substituted, where in the group -C (Z ² ) = C (Z ³ ) - or CZ ² Z ^3, the two radicals Z ² and Z ³ together a C ₄ - or C ₅ alkylene, C ₄ or C ₅ -alkenylene or C ₄ - or C ₅ -alkadiene-nylene bridge in which optionally one or two non-adjacent CH ₂ groups are replaced by oxygen atoms and / or carbonyl groups and in the case of alkenylene and

Alkadienylene bridge, the carbon atoms interconnected by the double bond (s) may be part of a six-membered, optionally benzo-fused, aromatic or heteroaromatic ring,

ZC ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ -alkyl-C ₁ -C ₂₀ -alkyl, C ₆ - C ₁₀ -aryl-C ₂ -C ₂₀ alkenyl, heteroaryl-Ci-C ₂₀ alkyl or heteroaryl-C ₂ -C ₂₀ alkenyl each having 2 to 12 carbon atoms in the heteroaryl radical,

Z ^'is hydrogen or, independently of Z, has the same meaning as Z,

Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which is benzanellated once or twice and is substituted by one or more halogen, NO ₂ , NO, CN, CHO, R ¹ , X ¹ -CO-R ¹ , X ¹ -SO ₂ -

R ¹ , X ¹ -R ^{1 '} , CO-X ¹ -R ^1' or SO ₂ -X ¹ -R ^{1 '} may be substituted,

E independently of one another -CO-O-, -O-C0-, -CO-S-, -S-CO-, -CO-NR ^' -, -

NR ^'is -CO- or -O-CO-O-,

R ^{1 is} C ₁ -C ₂ O-AlKyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, Ce-Cu-aryl-C-rCj-o-alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl, heteroaryl or heteroaryl-C ₂ -C ₂ o-alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the Ci-C ₂₀ - or C ₂ -C ₂₀ -Kohlen- chain one or more non-adjacent CH ₂ groups by oxygen atoms , N (C ₁ -C ₂₀ -alkyl) and / or carbonyl groups may be replaced and both the C ₆ -C ₁₀ -aryl and the heteroaryl with one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, XR ^' , CO-XR ^' or SO ₂ -XR ^' may be substituted,

R ^{1 'is} hydrogen or, independently of R ^1, the same meaning as R ¹ ,

RC ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ -aryl-C ₁ -C ₂₀ -alkyl, C ₆ -C ₁₀ - aryl-C ₂ -C ₂₀ -alkenyI, heteroaryl-C _r C ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ alkenyl each having 2 to 12 carbon atoms in the heteroaryl radical,

R 'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ^{1 '} or NR ^' , where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups are replaced by carbonyl groups and in the case of the alkenylene and alkadienylene bridges the carbon atoms joined together by the double bond (s) may be part of a six-membered, optionally benzanellated, aromatic or heteroaromatic ring,

With regard to the definition of the variables Z ¹ , Z ² and Z ³ or Z and Z ^' or W is analogously to those already above for the variables R ^1' and R ^{2 '} or R and R ^' or X ¹ , X ² and X given definitions and examples listed radicals; With regard to the remaining variables Ar ¹ , R ¹ , R ^{1 '} , R, R ^' , X ¹ and X and their preferences, reference may likewise be made to the radicals already mentioned by way of example.

A particularly suitable group of compounds corresponds to the general formula 6 in which the rings A ¹ and A ² can each independently be substituted by one or two C ₁ -C ₄ -alkyl or C ₁ -C ₄ -alkoxy and the variables mean Y is a single chemical bond, C ₂ -C ₄ -alkylene, SO ₂ or CZ ² Z ³ ,

Z ^2, Z ³ are independently C ₁ -C ₀ -alkyl or C ₆ -C ₁₀ aryl, wherein said C ₆ -C ₁₀ - aryl ^'substituted with one or more halogen, especially fluorine, Z, CO-Z or OZ and in the group CZ ² Z ³ the two radicals Z ² and Z ³ together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge in which one or two non-adjacent CH ₂ groups are replaced by oxygen atoms and / or carbonyl groups and, in the case of the alkenylene and alkadienylene bridges, the carbon atoms linked together by the double bond (s)

May be part of a six-membered optionally benzo-fused aromatic or heteroaromatic ring,

ZC _{r is} C _1o -alkyl or C ₆ -C ₁₀ -aryl,

Z 'is hydrogen or, independently of Z, has the same meaning as Z,

Ar ^{1 is} independently an aromatic or heteroaromatic five or six membered ring containing one or more halogens, in particular fluorine, R ¹ , X ¹ -CO-R \ X ¹ -R ^{1 '} or CO-X ¹ -R ^{1 '} can be substituted,

E is independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-,

R ^{1 is} independently C ₁ -C ₁₀ -alkyl, C ₂ -C _1o alkenyl, C ₆ -C ₁₀ -AryI, C ₆ -C ₀ - aryl-CrC ^ alkyl, or C ₆ -C _1o aryl-C ₂ -C _1o -alkenyl, where in the C ₁ -C ₁₀ - or

C ₂ -C ₁₀ carbon chain one or more non-adjacent CH ₂ groups may be replaced by oxygen atoms, N (C ₁ -C ₁₀ alkyl) - and / or carbonyl groups and the C ₆ -C ₁₀ aryl with one or more Halogen, R, X-CO-R, XR ^' or CO-XR ^' may be substituted,

R ^{1 'is} hydrogen or, independently of R ^1, the same meaning as R ¹ ,

RC _r C _1o -alkyl or C ₆ -C ₁₀ -alkyl,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen or NR ¹ 'or NR', where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ - Group corresponds, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ alkylene, C ₄ - or C ₅ alkenylene or C ₄ - or C ₅ -Alkadienylenbrücke, in which optionally replaces one or two non-adjacent CH ₂ groups with carbonyl groups and, in the case of the alkenylene and alkadienylene bridges, the carbon atoms interconnected by the double bond (s) may form part of a six-membered, optionally benzanellated, aromatic or heteroaromatic ring,

In the above-mentioned particularly suitable group of compounds of formula 6 are those of interest, wherein the rings A ¹ and A ² independently of one another in each case additionally substituted by one or two C ₁ -C ₄ -AlkVl or C ₁ -C ₄ -Akoxy can be and the variables mean

Y CZ ^ Z ^J

Z ^2, Z ³ independently of one another C ₁ -C ₁₀ -alkyl or C ₆ -C ₁₀ aryl, wherein said C ₁ -C ₁₀ - alkyl having one or more fluorine and the C ₆ -C ₁₀ aryl with one or more Fluorine, C ₁ -C ₁₀ -alkyl or C ₁ -C ₁₀ -alkoxy may be substituted and in the group CZ ² Z ^3, the two radicals Z ² and Z ³ together form a C ₄ - or C ₅ -alkylene-, C ₄ or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge in which one or two non-adjacent CH ₂ groups are replaced by oxygen atoms and / or carbonyl groups and in the case of the alkenylene and alkadienylene bridges by the double bond ( en) interconnected carbon atoms may be part of a six-membered optionally benzo-fused aromatic or heteroaromatic ring,

and the remaining variables have the meaning given in the above-mentioned particularly suitable group of compounds of formula 6.

Examples of such compounds are:

In the above-mentioned particularly suitable group of compounds of formula 6 are further of interest in which the rings A ¹ and A ² are each independently additionally substituted in each case with one or two C ₁ -C ₄ -AlkYl or Ci-C ₄ -Akoxy can be and the variables mean

and the remaining variables have the meaning given in the above-mentioned particularly suitable group of compounds of formula 6. Examples of such compounds are

Another suitable group of compounds having tetravalent organic radicals Ar ² corresponds to the general formula 7

(7)

each independently of one another is a C ₂ -C ₃ -alkylene or C ₂ -C ₃ -alkenylene bridge which is optionally substituted by one or two C ₁ -C ₄ -alkyl groups and in which optionally a CH ₂ group is replaced by oxygen or a C ₂ -C ₃ -alkenylene bridge Replaced carbonyl group and / or in the case of the C ₂ -C ₃ alkenylene bridge, the carbon atoms interconnected by the double bond may be part of a six-membered optionally benzanellierten aromatic or heteroaromatic ring and the other variables mean: Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which is benzanellated once or twice and is substituted by one or more halogen, NO ₂ , NO, CN, CHO, R ¹ , X ¹ -CO-R ¹ , X ¹ -SO ₂ -R ¹ , X ¹ -R ¹ ', CO-X ¹ -R ¹ ' or SO ₂ -X ¹ -R ^{1 '} may be substituted,

E independently of one another -CO-O-, -O-C0-, -CO-S-, -S-CO-, -CO-NR ^' -, -

NR'-CO- or -O-CO-O-,

R ^{1 is} C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, Ce-C ₁ -C aryl-C ₁ -C -alkyl, C C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl, heteroarylCrC ^ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the C ₁ -C ₂₀ one or more non-adjacent CH ₂ groups can be replaced by oxygen atoms, N (C ₁ -C ₂₀ -alkyl) and / or carbonyl groups and both the C ₆ - or C ₂ -C ₂₀ -carbon chain. C ₁₀ aryl and the heteroaryl having one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, XR ^' , CO-XR ^' or SO ₂ -XR 'can be substituted,

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

R is C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₀ aryl-C ₂ -C ₂₀ alkenyl, heteroaryl-CrC ^ alkyl, or heteroaryl-C ₂ -C ₂₀ -alkenyI each having 2 to 12 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR', where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ¹ ') ₂ - or N (R') ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ alkylene, C ₄ - or C ₅ alkenylene or C ₄ - or C ₅ -Alkadienylenbrücke, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

With regard to the definition of the variables Ar ¹ , R ¹ , R ¹ ', R, R', X ¹ and X and their preferences, reference is made to the definitions given above and the radicals listed by way of example. A particularly useful group of compounds represented by the general formula 7, further ₄ -alkoxy may be substituted wherein the rings A ¹ and A ² independently of one another have in each case with one or two C ₁ -C ₄ -AIRyI or C,

C ₂ -C ₃ -alkylene or C ₂ -C ₃ -alkenylene bridges which are optionally substituted by one or two C ₁ -C ₄ -alkyl groups and in which optionally a CH ₂ group is replaced by oxygen or a carbonyl group and / or in the case of C ₂ -C ₃ alkenylene bridges, the carbon atoms which are joined together by the double bond can be part of a six-membered aromatic or heteroaromatic ring and the other variables mean:

Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which may be substituted by one or more fluoro, R ¹ , X ¹ -CO-R ¹ , X ¹ -R ¹ 'or CO-X ¹ -R ¹ ' .

E is independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-,

R ^{1 is} C ¹ -C ₁₀ -alkyl, phenyl or phenyl-C ¹ -C 4 -alkyl, where the phenyl may be substituted by one or more fluorine, R, X-CO-R, XR 'or CO-XR',

R ^{1 'is} hydrogen or, independently of R ^1, the same meaning as R ¹ ,

RC ₁ -C ₁₀ alkyl or phenyl,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR', where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ¹ ') ₂ - or N (R') ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring. Examples of such compounds are



Another suitable group of compounds having tetravalent organic radicals Ar ² corresponds to the general formula 8

(8th)

wherein the rings A ³ and A ⁴ are each independently additionally each with one or two C ₁ -C ₄ -AlkYl or C ₁ -C ₄ -alkoxy and the rings A ¹ , A ^{1 '} , A ² and A ² ' in addition to the Groupings Ar ¹ -E independently still each with one or two

C ₁ -C ₄ -alkyl or C ₁ -C ₄ -alkoxy may be substituted, and the other variables mean:

independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO-, -CO-NR'-, - NR ^'CO- or -0-CO-O-, R ^{1 is} C ₁ -C ₆ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₁ -C 4 -arylCr-C ₆ -alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl, hetero- or heteroaryl-C ₂ -C ₂ o-alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the C ₁ -C _2O- or C ₂ -C ₂₀ -carbon chain one or more non-adjacent CH ₂ groups Oxygen atoms, N (C ₁ -C ₂₀ -alkyl) and / or carbonyl groups may be replaced and both the C ₆ -C ₁₀ -aryl and the heteroaryl with one or more halogen, NO ₂ , NO, CN, CHO, R, X- CO-R, X-SO ₂ -R, XR ^' , CO-XR ^' or SO ₂ -XR 'may be substituted,

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

R is C ₁ -C 4 -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C _1o aryl-C ₂ -C ₂ o-alkenyl, heteroaryl-CrC ^ alkyl, or heteroaryl-C ₂ -C ₂₀ alkenyl each having 2 to 12 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR', where in the event that X ¹ -R ^{1 '} or XR' of an N (R ^{1 '} ) ₂ - or N (R') ₂ group, the two radicals R ¹ 'and R' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

A particularly suitable group of compounds corresponds to the general formula 8, wherein the rings A ³ , A ⁴ , A ¹ , A ^{1 '} , A ² and A ² ' are each independently additionally each with one or two C ₁ -C ₄ -Alk ^ or C ₁ -C ₄ -alkoxy may be substituted, and the other variables mean: Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which may be substituted by one or more fluoro, R ¹ , X ¹ -CO-R ¹ , X ¹ -R ¹ 'or CO-X ¹ -R ¹ ' .

E is independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-,

R ^{1 is} C ₁ -C ₁₀ -alkyl, phenyl or phenyl-C ₁ -C 4 -alkyl, where the phenyl may be substituted by one or more fluorine, R, X-CO-R, XR 'or CO-XR',

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

RC ₁ -C ₁₀ alkyl or phenyl,

R 'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR', where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

Examples of such compounds are

Another suitable group of compounds having tetravalent organic radicals Ar ² corresponds to the general formula 9

(9)

in which the rings A ¹ and A ^{2 may} be additionally substituted, in each case additionally, in each case with a C ₁ -C ₄ -alkyl or C ₁ -C ₄ -alkoxy, and the other variables mean:

Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which is benzanellated once or twice and is substituted by one or more halogen, NO ₂ , NO, CN ₁ CHO, R ¹ , X ¹ -CO-R ¹ , X ¹ -SO ₂ -

R ¹ , X ¹ -R ^{1 '} , CO-X ¹ -R ¹ ' or SO ₂ -X ¹ -R ^{1 '} may be substituted, E independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO-, -CO-NR ^' -,

-NR ^' -CO- or -O-CO-O-,

R ^{1 is} C ₁ -C ₂₀ -alkyl, C ₂ -C ₂ o-alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, Ce-C ₁ -C aryl-C ₁ -C 4 -alkyl, C ₆ C _1o -aryl-C ₂ -C ₂ o-alkenyl, heteroaryl-dC ^ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the C ₁ -C ₂₀ or C ₂ -C ₂₀ -carbon chain one or more non-adjacent CH ₂ groups can be replaced by oxygen atoms, N (C ₁ -C ₂₀ -Alkyl) - and / or carbonyl groups and both the C ₆ -C ₁₀ -Aryl and the heteroaryl having one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, XR ^' , CO-XR' or SO ₂ -XR ' may be substituted

R ^{1 'is} hydrogen or, independently of R ^1, the same meaning as R ¹ ,

RC _r C ₂₀ alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having from 2 to 12 carbon atoms, C ₆ -C ₀ aryl-Ci-C ₂₀ alkyl, C ₆ -C ₁₀ -Aryl-C ₂ -C ₂₀ -alkenyl, heteroarylCrC ^ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

R 'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR', where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ¹ ') ₂ - or N (R') ₂ group, the two radicals R ^{1 '} and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

A particularly suitable group of compounds corresponds to the general formula 9, in which the rings A ¹ and A ² bear no further substituents apart from the groupings Ar ¹ -E and the other variables mean: Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which may be substituted by one or more fluoro, R ¹ , X ¹ -CO-R ¹ , X ¹ -R ¹ 'or CO-X ¹ -R ^1' .

E is independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-,

R ^{1 is} C ₁ -C ₁₀ -alkyl, phenyl or phenyl-C ₁ -C 4 -alkyl, where the phenyl may be substituted by one or more fluorine, R, X-CO-R, XR ^' or CO-XR ^' ,

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

RC ₁ -C ₁₀ alkyl or phenyl,

R 'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR', where in the event that X ¹ -R ^{1 '} or XR' of an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ group, the two radicals R ^{1 '} and R ^' together can form a C ₄ - or C ₅ -alkyiene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

Examples of such compounds are

A suitable group of compounds having hexavalent organic radicals Ar ² corresponds to the general formula 10

in which the rings A ¹ and A ² can additionally be additionally substituted in each case with a C ₁ -C ₄ -alkyl or C ₁ -C ₄ -alkoxy,

each independently of one another represents a C ₂ -C ₃ -alkylene or C ₂ -C ₃ -alkenylene bridge which is optionally substituted by one or two C ₁ -C ₄ -alkyl groups and in which optionally a CH ₂ group is replaced by oxygen or a C ₁ -C ₄ -alkyl group Replaced carbonyl group and / or in the case of the C ₂ -C ₃ alkenylene bridge, the carbon atoms interconnected by the double bond may be part of a six-membered optionally benzene fused aromatic or heteroaromatic ring and the remaining variables mean:

independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO-, -CO-NR'-, - NR ^'is -CO- or -O-CO-O-,

R ^{1 is} C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₀ aryl, heteroaryl having from 2 to 12 carbon atoms, C6-C _1o -aryl-C ₂ -C ₂ o-alkenyl, heteroarylCrC ^ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the C ₁ -C One or more non-adjacent CH ₂ groups can be replaced by oxygen atoms, N (C ₁ -C ₂₀ -alkyl) and / or carbonyl groups and both the C ₆ -C ₂₀ - or C ₂ -C ₂₀ -Kohlen- ₁₀ -aryl and the heteroaryl having one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, X-R ', CO-XR' or SO ₂ - XR ^' may be substituted,

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ , RC _r C ₂ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having from 2 to 12 carbon atoms, C ₆ -C _O _{aryl-Ci-C2o-alkyl,} C ₆ - C ₁ -C aryl-C ₂ -C ₂ o-alkenyl, heteroaryl-C ₁ -C 4 -alkyl or heteroaryl C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

R 'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR', where in the event that X ¹ -R ¹ 'or XR ^{' of} an N (R ¹ ') ₂ - or N (R') ₂ group, the two radicals R ¹ 'and R' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of Aikenylen- and Alkadieny len bridge the interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

With regard to the definition of the variables Ar ¹ , R ¹ , R ¹ ', R, R', X ¹ and X and their preferences, reference is made to the definitions given above and the radicals listed by way of example.

A particularly suitable group of compounds corresponds to the general formula 10, in which the rings A ¹ and A ^{2, in} addition to the arylations Ar ¹ -E independently of one another, additionally each having a C ₁ -C ₄ -alkyl or C ₁ -C ₄ - Alkoxy can be substituted,

C ₂ -C ₃ -alkylene or C ₂ -C ₃ -alkenylene bridges which are optionally substituted by one or two C ₁ -C ₄ -alkyl groups and in which optionally a CH ₂ group is replaced by oxygen or a carbonyl group and / or in the case of C ₂ -C ₃ alkenylene bridges, the carbon atoms connected by the double bond may be part of a six-membered aromatic or heteroaromatic ring and the remaining variables mean:

E is independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-, R ^{1 is} C ₁ -C ₁₀ alkyl, phenyl or where the phenyl may be substituted by one or more fluoro, R, X-CO-R, XR 'or CO-XR ^' ,

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

R is _CrC 1o -alkyl or phenyl,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ^{1 '} or NR', where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ¹ ') ₂ - or N (R') ₂ group, the two radicals R ¹ 'and R ^' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

Examples of such compounds are

Another suitable group of compounds having hexavalent organic radicals Ar ² corresponds to the general formula II

(11)

wherein the rings A ¹ , A ^{1 '} , A ² , A ^2' , A ³ and A ^{3 '} independently of one another in each case additionally with one or two C ₁ -C ₄ -AIKyI or C ₁ -C ₄ -alkoxy may be substituted and the remaining variables mean:

Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which is benzanellated once or twice and is substituted by one or more halogen, NO ₂ , NO, CN, CHO, R ¹ , X ¹ -CO-R ¹ , X ¹ -SO ₂ -R ¹ , X ¹ -R ^{1 '} , CO-X ¹ -R ^1' or SO ₂ -X ¹ -R ^{1 '} may be substituted, E independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO-, -CO-NR ^' -,

-NR ^' -CO- or -O-CO-O-,

E 'independently of each other a single chemical bond, oxygen, sulfur, NR' or C ₁ -C ₂₀ -AIKyI, wherein in the Ci-C ₂₀ carbon chain one or more non-adjacent CH ₂ groups by oxygen atoms, N (C ₁ -C _20- alkyl) and / or carbonyl groups may be replaced,

R ^{1 is} C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having 2 to 12 atoms of carbon, C ₆ -C _1o _{aryl-Ci-C2o-alkyl} , C ₆ -C _1o -aryl-C ₂ -C ₂ o-alkenyl, heteroaryl-CrCj-o-alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the C _One or more non-adjacent CH ₂ groups can be replaced by oxygen atoms, N (C ₁ -C ₂₀ -alkyl) and / or carbonyl groups and both the C ₁ -C ₂₀ - or C ₂ -C ₂₀ -carbon chain ₆ -C _1o -aryl and the heteroaryl having one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, XR ^' , CO-XR ^' or SO ₂ -XR 'may be substituted,

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

RC ₁ -C ₂₀ -AlkYl, C ₂ -C ₂₀ alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ aryl-Ci-C ₂₀ alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl, heteroaryl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

R 'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR ^' , where in the event that X ¹ -R ^{1 '} or XR' of an N (R ^{1 '} ) ₂ - or N (R') ₂ group, the two radicals R ^{1 '} and R' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring.

With regard to the definition of the variables Ar ¹ , R ¹ , R ¹ ', R, R', X ¹ and X and their preferences, reference is made to the definitions given above and the radicals listed by way of example. A particularly suitable group of compounds corresponds to the general formula 11, wherein the rings A ¹ , A ^{1 '} , A ² , A ² ', A ³ and A ^{3 '} are each independently additionally each with one or two C ₁ -C ₄ - AIKyI or C ₁ -C ₄ -alkoxy can be substituted and the other variables mean:

E is independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-,

E 'is independently a chemical single bond, oxygen or CrC-io-alkyl, wherein the Ci-C ₁₀ carbon chain, one or more non-adjacent CH ₂ groups are replaced by oxygen atoms, N (C ₁ -C ₁₀ -alkyl) - and / or carbonyl groups can be replaced,

R ^{1 is} C ₁ -C ₁₀ alkyl, C ₆ -C ₁₀ aryl, heteroaryl of 2 to 5 carbon atoms, C ₁ -C ₄ arylCrC-m-alkyl, C ₆ -C ₁₀ aryl-C ₂ -C ₁₀ -alkenyl, heteroaryl-C _r C _{1 o} -alkyl or heteroaryl-C ₂ -C ₁₀ -alkenyl having in each case 2 to 5 carbon atoms in the heteroaryl radical, where in the C ₁ -C ₁₀ - or C ₂ -C ₀ - Carbon chain one or more non-adjacent CH ₂ groups can be replaced by oxygen atoms, N (C ₁ -C _1o alkyl) and / or carbonyl groups and both the C ₆ -C ₁₀ aryl and the heteroaryl with one or more halogen .

CN, R, X-CO-R, X-R 'or CO-X-R' may be substituted,

R ^{1 'is} hydrogen or, independently of R ^1, the same meaning as R ¹ ,

R is C ₁ -C ₁₀ -alkyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 5 carbon atoms,

Ce-C-io-arylCrC-io-alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₁₀ -alkenyl, heteroaryl-C ₁ -C 4 -alkyl or heteroaryl-C ₂ -C ₁₀ -alkenyl, each having 2 to 5 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR', where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ group, the two radicals R ^{1 '} or R ^' together can form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups are replaced by carbonyl groups and, in the case of the alkenylene and alkadienylene bridges, the carbon atoms interconnected by the double bond (s) may form part of a six-membered, optionally benzanellated, aromatic or heteroaromatic ring.

An example of such connections is

Another suitable group of compounds having hexavalent organic radicals Ar ² corresponds to the general formula 12

₂

(E-ArI) ₂

(12) wherein the rings A ^1, A ² and A ³ independently of one another may additionally be substituted by one or two C _r C ₄ alkyl or Ci-C ₄ -alkoxy or respectively mean and the remaining variables:

Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which is benzanellated once or twice and is substituted by one or more halogen, NO ₂ , NO, CN, CHO, R ¹ , X ¹ -CO-R ¹ , X ¹ -SO ₂ -R ¹ , X ¹ -R ¹ ', CO-X ¹ -R ¹ ' or SO ₂ -X ¹ -R ¹ 'may be substituted,

E independently of one another -CO-O-, -O-C0-, -CO-S-, -S-CO-, -CO-NR'-, -

NR'-CO- or -O-CO-O-,

R ¹ is C _r C ₂ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ aryl, heteroaryl having from 2 to 12 carbon atoms, C ₆ -C _1o aryl-C ₁ -C ₂ o alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₂ o-alkenyl, heteroarylC _r C ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, where in the CrC ₂₀ - or C ₂ -C ₂₀ carbon chain -Kohlen- one or more non-adjacent CH ₂ groups are replaced by oxygen atoms, N (Ci-C ₂₀ alkyl) - and / or carbonyl groups can be replaced, and both the C ₆ -C ₁₀ -Aryl and the heteroaryl having one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, XR ^' , CO-XR' or SO ₂ -XR 'can be substituted,

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

R is C ₁ -C 4 -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ -arylC _r C ₂₀ -alkyl, C ₆ -C ₁₀ - Aryl-C ₂ -C ₂₀ -alkenyl, heteroarylC _r C ₂ o-alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical,

R 'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR ^' , where in the event that X ¹ -R ¹ 'or XR ^{' of} an N (R ^{1 '} ) ₂ - or N (R ^' ) ₂ group, the two radicals R ¹ 'and R' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny len bridge interconnected by the double bond (s) carbon atoms may be part of a six-membered optionally benzanellier- th aromatic or heteroaromatic ring. With regard to the definition of the variables Ar ¹ , R ¹ , R ¹ ', R, R', X ¹ and X and their preferences, reference is made to the definitions given above and the radicals listed by way of example.

A particularly suitable group of compounds corresponds to the general formula 12, wherein the rings A ¹ , A ² and A ^{3 may be} independently of one another in each case additionally substituted by one or two C _r C ₄ alkyl or C ₁ -C ₄ -alkoxy and the remaining variables mean:

Ar ^{1 is} independently an aromatic or heteroaromatic five- or six-membered ring which is benzanellated once or twice and which contains one or more halogen, CN, R ¹ , X ¹ -CO-R ¹ , X ¹ -R ¹ 'or CO-X ¹ R ¹ 'may be substituted,

E independently of one another -CO-O-, -O-CO-, -CO-S-, -S-CO- or -O-CO-O-,

R ^{1 is} C ₁ -C ₁₀ -alkyl, C ₆ -C ₁₀ -ArVl, heteroaryl having 2 to 5 carbon atoms,

Ce-C _t o-aryl-CrC ^ alkyl, C ₆ -C _1o aryl-C ₂ -Cio-alkenyl, heteroaryl-CRCI _θ -alkyl or heteroaryl-C ₂ -C ₀ alkenyl each having 2 to 5 carbon atoms, in heteroaryl radical, one or more non-adjacent CH ₂ groups in the C ₁ -Ci ₀ or C ₂ -Ci ₀ carbon chain being substituted by oxygen atoms, N (C ₁ -C ₁₀ -alkyl) and / or carbonyl groups and both the C ₆ -C ₁₀ -aryl and the heteroaryl may be substituted by one or more halogen, CN, R, X-CO-R, XR ^' or CO-XR ^' ,

R ¹ 'is hydrogen or, independently of R ^1, the same meaning as R ¹ ,

R Ci-C ₁₀ alkyl, C ₆ -C ₀ aryl, heteroaryl having from 2 to 5 carbon atoms,

C ₆ -Cio-aryl-Ci-Ci _o alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₀ alkenyl, heteroaryl-C _r C _1o alkyl, or heteroaryl-C ₂ -C ₀ alkenyl having in each case 2 to 5 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, the same meaning as R

and

X ¹ , X independently of one another oxygen, sulfur or NR ¹ 'or NR ^' , where in the event that X ¹ -R ^{1 '} or XR ^{' of} an N (R ¹ ') ₂ - or N (R') ₂ group, the two radicals R ¹ 'and R' together may form a C ₄ - or C ₅ -alkylene, C ₄ - or C ₅ -alkenylene or C ₄ - or C ₅ -alkadienylene bridge, in which optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of alkenylene and Alkadieny- The carbon atoms connected by the double bond (s) may be part of a six-membered, optionally benzanellated, aromatic or heteroaromatic ring.

Examples of such compounds are

A further subject of the present invention is a light-emitting layer which comprises at least one of the compounds of the formula I or a preferred guide form as a matrix material and at least one further substance distributed therein as an emitter.

In particular, the light-emitting layer according to the invention contains at least one of the compounds from the abovementioned groups of compounds of the formulas 1 to 12 or a preferred embodiment as matrix material and at least one further substance distributed therein as emitter.

Another object of the present invention is a light-emitting layer which consists of at least one of the compounds of formula I or a preferred embodiment as a matrix material and at least one further substance distributed therein as an emitter.

In particular, the light-emitting layer according to the invention consists of at least one of the compounds from the abovementioned groups of compounds of the formulas 1 to 12 or a preferred embodiment as matrix material and at least one further substance distributed therein as emitter.

Of course, the matrix material according to the present invention can also be used in combination with other matrix materials known to the person skilled in the art. The use of the compounds of the formula I as matrix materials is not intended to preclude these compounds themselves also emitting light. However, the matrix materials used according to the invention have the effect that, in the case of compounds which are used as emitters in OLEDs, an increase in the luminance and quantum yield compared with otherwise conventional matrix materials is normally achieved if they are embedded in the former.

Many of these emitter compounds are based on metal complexes, and in particular the complexes of the metals Ru, Rh, Ir, 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 as matrix materials for emitters based on such metal complexes. In particular, they are suitable for use as matrix materials together with complexes of Ru, Rh, Ir, Pd and Pt, more preferably for use with complexes of Ir.

Suitable metal complexes for use together with the compounds of the formula I as matrix materials in OLEDs are described, for example, in the publications WO 02/60910 A1, WO 02/68453 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 and WO 02/15645 A1. Suitable metal complexes for use together with the compounds of the formula I as matrix materials in OLEDs are, for example, also carbene complexes, as described in WO 05/019373 A2. The disclosure of this publication is hereby explicitly referred to and the disclosure of which is to be considered incorporated into the content of the present application. In particular, suitable metal complexes for use together with the compounds of the formula I as matrix materials in OLEDs contain carbene ligands of the following structures disclosed in the document WO 05/019373 A2 (the designation of the variables was taken from the document WO 05/019373 A2; the more precise definition of the variables is explicitly referred to this publication):

in which mean:

the attachment sites of the ligand to the metal center;

z, z are the same or different, CH or N;

R ₁ R is the same or different, an alkyl, aryl, heteroaryl or alkenyl radical, preferably an alkyl or aryl radical or in each case 2 radicals R ¹² or R ^{12 '} form Together, a fused ring which may optionally contain at least one heteroatom, preferably N, preferably in each case 2 radicals R ¹² and R ¹² together form a fused aromatic C ₆ ring, wherein to this, preferably six-membered, aromatic ring optionally or several other aromatic rings may be fused, with any conceivable annulation being possible, and the fused radicals may in turn be substituted; or R ¹² or R ¹² is a radical with donor or acceptor action, preferably selected from the group consisting of halogen radicals, preferably F, Cl, Br, particularly preferably F; Alkoxy, aryloxy, carbonyl, ester, amino, amide, CHF ₂ , CH ₂ F, CF ₃ , CN,

Thio groups and SCN;

t and t 'are identical or different, preferably equal to 0 to 3, where, when t or t'> 1, the radicals R ¹² and R ^{12 may be} identical or different, preferably t or f is 0 or 1 the radical R ¹² or R ^{12 '} is, when t or f is 1, in the ortho, meta or para position to the point of attachment to the nitrogen atom adjacent to the carbene carbon atom;

R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ and R ^{11 are} hydrogen, alkyl, aryl, heteroaryl, alkenyl or a substituent with donor or acceptor action, preferably selected from halogen radicals, preferably F, Cl, Br, especially preferred are F, alkoxy radicals, aryloxy radicals, carbonyl radicals, ester radicals, amine radicals, amide radicals, CH ₂ F groups, CHF ₂ groups, CF ₃ groups, CN groups, thio groups and SCN groups

Hydrogen, alkyl, heteroaryl or aryl,

R ^{10 is} alkyl, aryl, heteroaryl or alkenyl, preferably alkyl, heteroaryl or aryl, or in each case 2 radicals R ¹⁰ together form a fused ring which may optionally contain at least one heteroatom, preferably nitrogen, preferably form in each case 2 radicals R ¹⁰ together, a fused aromatic C ₆ ring, which may be fused to this, preferably six-membered, aromatic ring optionally one or more further aromatic rings, with any conceivable annulation is possible, and the fused radicals may in turn be substituted; or R ¹⁰ is a radical having a donor or acceptor effect, preferably selected from the group consisting of halogen radicals, preferably F, Cl, Br, particularly preferably F; Alkoxy, aryloxy, carbonyl, ester, amino, amide, CHF ₂ , CH ₂ F, CF ₃ , CN, thio groups and SCN v is 0 to 4, preferably 0, 1 or 2, most preferably 0, wherein when v

0, the four carbon atoms of the aryl group in formula c, optionally substituted with R ¹⁰ , carry hydrogen atoms.

In particular, suitable metal complexes for use together with the compounds of the formula I as matrix materials in OLEDs contain Ir carbene complexes of the following structures disclosed in the document WO 05/019373 A2:

where the variables have the meanings already mentioned above.

Further suitable metal complexes for use together with the compounds of the formula I as matrix materials in OLEDs are in particular also:

88



where M is Ru (III), Rh (III), Ir (III), Pd (II) or Pt (II), n is Ru (III), Rh (III) and Ir (III) is 3, for Pd (II) and Pt (II) assumes the value 2 and Y ² and Y ³ signify hydrogen, methyl, ethyl, n-propyl, isopropyl or tert-butyl. Preferably, M is Ir (III) with n equal to 3. Y ³ is preferably methyl, ethyl, n-propyl, iso-propyl or tert-butyl.

X = O ₁ S

where M is Ru (III), Rh (III), Ir (III), Pd (II) or Pt (II), n is Ru (III) ₁ Rh (III) and Ir (III) is 3, for Pd (II) and Pt (II) is 2 and Y ^{3 is} hydrogen, methyl, ethyl, n-propyl, iso-propyl or tert-butyl. Preferably, M is Ir (III) with n equal to 3. Y ³ is preferably methyl, ethyl, n-propyl, iso-propyl or tert-butyl.

wherein M is Ru (III), Rh (III) and especially Ir (III), Pd (II) or Pt (II), n is Ru (III), Rh (III) and Ir (III) is 3 and for Pd (II) and Pt (II) assumes the value 2.

where M is Ru (II), Rh (III) and especially Ir (III), Pd (II) or Pt (II), n is Ru (III), Rh (III) and Ir (III) are 3 and for Pd (II) and Pt (II) assumes the value 2.

Furthermore, complexes with different carbene ligands and / or with ligands L come into question, the latter being mono- or dianionic and may be both mono- and bidentate.

The following table gives schematically complexes ML '(L ") ₂ with trivalent metal centers and two different carbene ligands L' and L" where M is, for example, Ru (III), Rh (III) or Ir (III), in particular Ir (III), and L ^' and L "are, for example, ligands selected from the group of ligands L ¹ to L ⁷

Y ^{2 is} hydrogen, methyl, ethyl, n-propyl, iso-propyl or tert-butyl and Y ^{3 is} methyl, ethyl, n-propyl, iso-propyl or tert-butyl. designated. A representative of these complexes with different carbene ligands (L '= L ⁴ with Y ² = hydrogen and Y ³ = methyl, L ^" = L ² with Y ² = hydrogen and Y ³ = methyl) is, for example:

Of course, in the complexes of trivalent metal centers (for example in the case of Ru (III), Rh (III) or Ir (III)) used as emitter in the matrix materials of the formula I, all three carbene ligands may also be different from one another.

Examples of complexes of trivalent metal centers M with ligands L (here monoanionic, bidentate ligand) as "spectator ligands" are LML ^' L ", LM (L') ₂ and L ₂ ML ', where M is approximately Ru (III), Rh (III) or Ir (III), in particular Ir (III), and L ^' and L "have the meaning given above. For the combination of L 'and L "in the complexes LML'L" this yields:

Suitable ligands L are, in particular, the acetylacetonate and its derivatives, the picolinate, Schiff's bases, amino acids and the bidentate monoanionic ligands mentioned in WO 02/15645; In particular, the acetylacetonate and pico linat of interest. In the case of complexes L ₂ ML ', the ligands L may be the same or different.

A representative of these complexes with different carbene ligands (L '= L ⁴ with Y ² = hydrogen and Y ³ = methyl, L ^" = L ² with Y ² = hydrogen and Y ³ = methyl) is, for example:

wherein z ¹ and z ² in the symbol

stand for the two teeth of the ligand L. Y ³ denotes hydrogen, methyl, ethyl, n-propyl, isopropyl or tert-butyl, in particular methyl, ethyl, n-propyl or isopropyl. Organic light emitting diodes (OLEDs) are basically made up of several layers, eg:

1. anode 2. hole-transporting layer

3. Light-emitting layer

4. Electron-transporting layer

5th 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 said layers, for example, an OLED having the layers (1) (anode), (3) (light emitting layer), and (5) (cathode) is also suitable the layers (2) (hole-transprotective layer) and (4) (electron-transprotective layer) are taken over by the adjacent layers. OLEDs comprising layers (1), (2), (3) and (5) or layers (1), (3), (4) and (5) are also suitable.

With suitable substitution, the compounds of the formula I _{1 can be used} in particular as such compounds of the groups of compounds of the formulas 1 to 12 described above as charge-transporting materials, but are preferably used as matrix materials in the light-emitting layer.

The compounds of the formula I used according to the invention, in particular those compounds of the above-described groups of compounds of the formulas 1 to 12, can be present as the sole matrix material in the light-emitting layer without further additives. 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 can be a polymer, for example poly (N-vinylcarbazole) or polysilane. However, the diluent material can 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 in the light-emitting layer according to the invention is generally still at least 40% by weight, preferably 50 to 100% by weight, based on the total weight of the compound of the formula I and diluent ,

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 constructed of a layer into which holes 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 adapted to the working function of the anode and the LUMO (lowest unoccupied molecular orbital) of the electron-transporting layer to the work function of the cathode.

Furthermore claimed are organic light-emitting diodes which contain such light-emitting layers according to the invention.

Another object of the present application are OLEDs containing a light-emitting layer which at least one compound of formula I or its preferred embodiments, in particular those compounds of the above-described groups of compounds of formulas 1 to 12, as a matrix material and at least one further therein contains distributed substance as an emitter, or which consists of one or more compounds of formula I or its preferred embodiments, in particular those compounds of the above-described groups of compounds of formulas 1 to 12, as a matrix material and at least one further substance distributed therein as an emitter.

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, IIIb and IVb of the Periodic Table of the Elements (old IUPAC 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.

Suitable hole transport materials for the layer (2) of the OLED 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 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 ₁ 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 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.

Suitable electron transport materials for the layer (4) of the OLEDs according to the invention comprise chelated metals with oxinoid compounds, such as tris (8-quinolinolato) aluminum (Alq ₃ ), 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). In this case, the layer (4) can serve both to facilitate the electron transport and as a buffer layer or as a barrier layer in order to avoid quenching of the exciton at the interfaces of the layers of the OLED. Preferably, the layer (4) improves the mobility of the electrons and reduces quenching of the exciton.

Of the materials mentioned above as hole transport materials and electron transport materials, some may serve several functions. For example, some of the electron-conducting materials are simultaneously hole-blocking materials if they have a deep HOMO. 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 transport materials can be doped with electron acceptors, for example phthalocyanines or arylamines such as TPD or TDTA can be doped with tetrafluorotetracyanchinodimethane (F4-TCNQ). For example, the electron transport materials may be doped 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 (5) 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 bandgap between the layers. Alternatively, this layer can serve as a protective layer.

In a preferred embodiment, in addition to the layers (1) to (5), 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); a block layer for holes between the light-emitting layer (3) and the

Electron-transporting layer (4); an electron injection layer between the electron-transporting

Layer (4) and the cathode (5).

However, it is also possible that the OLED does not have all of the layers (1) to (5) mentioned, for example an OLED with the layers (1) (anode), (3) (non-emissive layer) and (5 ) (Cathode), wherein the functions of the layers (2) (hole-transporting layer) and (4) (electron-transporting layer) are taken over by the adjacent layers. OLEDs comprising layers (1), (2), (3) and (5) or layers (1), (3), (4) and (5) are also suitable.

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, each of the mentioned layers of the OLED according to the invention can be developed from two or more layers. Furthermore, it is possible that some or all of the layers (1), (2), (3), (4), and (5) are surface treated to increase the efficiency of 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 or polymer films. For vapor deposition, conventional techniques can be used such as thermal evaporation, chemical vapor deposition and others. In an alternative method, the organic layers may be coated 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) 500 to 5000 A, preferably 1000 to 2000 A; Hole-transporting layer (2) 50 to 1000 A, preferably 200 to 800 A, light-emitting layer (3) 10 to 1000 A, preferably 100 to 800 A, electron-transporting layer (4) 50 to 1000 A _1, preferably 200 to 800 A, cathode (5) 200 to 10,000 A, preferably 300 to 5000 A. The position of the recombination zone of holes and electrons in the inventive OLED and thus the emission spectrum of the OLED can be affected by the relative thickness of each layer. That is, the thickness of the electron transport layer should preferably be selected so that the electron / holes recombination zone is in the light emitting layer. The ratio of the layer thicknesses of the individual layers in the OLED depends on the materials used. The layer thicknesses of optionally used additional layers are known to the person skilled in the art.

By using the compounds of the formula I used as matrix materials in the light-emitting layer of the OLEDs according to the invention, OLEDs can be obtained with high efficiency. The efficiency of the OLEDs according to the invention can be further improved by optimizing the other 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. 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 the formula I used according to the invention 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

The preparation of two different OLEDs was carried out using a compound of the formula

(for preparation, see Ir complex (7) in document WO 05/010379 A2)

as a hole conductor and exciton / electron blocker,

a matrix material of the formula used according to the invention

and an emitter compound of the formula

The ITO substrate used as the anode was first cleaned with commercial cleaning agents for LCD production (Deconex 20NS ^® and neutralizing agent 25ORGAN- ACID ^®), and then in an acetone / isopropanol mixture in an ultrasonic bath cleaned. To remove possible organic residues, the substrate was subjected to a continuous ozone flow in an ozone furnace for a further 25 minutes. This treatment also improved hole injection of the ITO.

The vapor deposition rate was about 2 nm / min for all substances, the pressure about 10 ^"7 mbar.

To prepare both OLEDs, the hole conductor and exciton / electron blocker (235 ° C. crucible temperature) were first vapor-deposited onto the cleaned substrate to a thickness of 28 nm. Then, the deposition of a 20 nm thick layer of a micro research was carried out from 67 wt .-% of matrix material (120 ⁰ C pot temperature) and 33 wt .-% emitter connection (240 ⁰ C pot temperature).

In the case of OLED I, a BCP layer was subsequently applied as electron conductor and hole blocker in a thickness of 60 nm (120 ° C. crucible temperature) (BCP = 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline). ,

In the case of OLED II, a layer of the compound of the formula

(For the preparation, see in the earlier German patent application 10 2004 057073.6 Example 5b)) in a thickness of 5 nm (260 ° C crucible temperature) and a further layer of the compound of formula

in a thickness of 40 nm (17O ⁰ C crucible temperature) applied. In the case of both OLEDs then a 0.75 nm thick lithium fluoride layer and finally a 110 nm thick Al electrode was evaporated.

To characterize the OLED, electroluminescence spectra were recorded at different currents or voltages. Furthermore, the current-voltage characteristic was measured in combination with the radiated light output. The light output can be converted by calibration with a luminance meter into photometric quantities.

For the two OLEDs, the following electro-optical data results:

Claims

claims

1. Use of compounds of general formula I.

(Ar ⁱ -E-) _n -Ar ² (I)

Ar ^{1 is} an aromatic or heteroaromatic five- or six-membered

A ring which is benzanellated once or twice and which contains one or more halogen, NO ₂ , NO, CN, CHO, R ¹ , X ¹ -CO-R ¹ , X ¹ -SO ₂ -R ¹ , X ¹ -R ¹ ', CO-X ¹ -R ¹ 'or SO ₂ -X ¹ -R ^1' may be substituted,

Ar ^{2 is} an n-valent organic radical containing one or more aromatic and / or heteroaromatic five- or six-membered rings containing one or more halogen, NO ₂ , NO, CN, CHO, R ² , CO-R ² , X ² -SO ₂ -R ² , X ² -R ² 'or SO ₂ -X ² -R ² ' may be substituted,

E is -CO-O-, -O-C0-, -CO-S-, -S-CO-, -CO-NR ^' -, -NR'-CO-, -O-CO-O- or

R ^{1 is} C ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ -aryl-C ₂ -C ₂₀ -alkenyl,

Heteroaryl-CrC ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, wherein in the C ₁ -C ₂₀ - or C ₂ -C ₂₀ carbon chain one or more non-adjacent CH ₂ Groups can be replaced by oxygen atoms, N (C ₁ -C ₂₀ -alkyl) and / or carbonyl groups and both the C ₆ -C ₁₀ -aryl and the heteroaryl with one or more halogen, NO ₂ , NO, CN, CHO, R, X-CO-R, X-SO ₂ -R, XR ^' , CO-XR ^' or SO ₂ -XR ^' may be substituted,

R ² Ci-C ₂₀ alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₀ aryl, heteroaryl lenstoffatomen having 2 to 12 coal, C ₆ -C ₁ o-aryl-C ₁ -C ₂ o alkyl, C ₆ -C ₁₀ -aryl-C ₂ -C ₂ o-alkenyl,

Heteroaryl-C ₁ -C ₂₀ -alkyl or heteroaryl-C ₂ -C ₂₀ -alkenyl having in each case 2 to 12 carbon atoms in the heteroaryl radical, one or more nonadjacent ones in the C ₁ -C ₂₀ or C ₂ -C ₂₀ -carbon chain CH ₂ groups can be replaced by oxygen atoms, N (C ₁ -C ₂₀ -alkyl) and / or carbonyl groups and both the C ₆ -C ₁₀ -aryl and the heteroaryl with one or more halogen, NO ₂ , NO, CN, CHO, R, CO-R, X-SO ₂ -R, XR ^' or SO ₂ -XR ^' may be substituted,

R ^{1 '} , R ^{2' are} independently hydrogen or independently of R ¹ or

R ^{2 has} the same meaning as R ¹ or R ² ,

RC ₁ -C ₂₀ -alkyl, C ₂ -C ₂₀ -alkenyl, C ₆ -C ₁₀ -aryl, heteroaryl having 2 to 12 carbon atoms, C ₆ -C ₁₀ -alkyl-C ₁ -C ₂ o -alkyl, C ₆ - C _{1 o} aryl-C ₂ -C ₂₀ alkenyl, heteroaryl-CrC _ü o-alkyl or heteroaryl-C ₂ -C ₂₀ alkenyl each having 2 to 12 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, has the same meaning as R,

X ¹ , X ² , X independently of one another oxygen, sulfur or NR ^{1 '} or NR ^2' or NR ^' , where in the event that X ¹ -R ^1' or X ² -R ^{2 '} or XR ^' an N (R ¹ V or N (R ² V or N (R ^' ) ₂ group corresponds, the two radicals R ^1' and R ^{2 '} or R ^' together a C ₄ - or C ₅ alkylene - form, C ₄ - or C ₅ alkenylene or C ₄ - or C ₅ -Alkadienylenbrücke nen, in which optionally one or two non-adjacent

CH ₂ groups may be replaced by carbonyl groups and nylen- in the case of alkenyl and Alkadienylenbrücke which may be a six-membered, optionally benzo-fused aromatic or hetero- aromatic ring through the double bond (s) interconnected carbon atoms ingredient

and

2. Use of compounds of the formula I according to claim 1, wherein the variables have the following meanings

Ar ^{1 is} an aromatic or heteroaromatic five- or six-membered

Ring which may be benzo-benzylated and substituted by one or more halo, CN, R ¹ , X ¹ -CO-R ¹ , X ¹ -R ^{1 '} or CO-X ¹ -R ^1' ,

E -CO-O-, -O-CO-, -CO-S-, -S-CO- or

the latter grouping via the two positions marked with asterisks on two adjacent carbon atoms of Ar ¹ or

Ar ² and via the nitrogen atom to Ar ² or Ar ^{1 is} attached,

R ^{1 is} C ₁ -C ₁₀ -alkyl, C ₂ -C ₁₀ alkenyl, phenyl, heteroaryl having from 3 to 5 carbon atoms, phenyl-Ci-C ₁₀ alkyl, phenyl-C ₂ -C ₁₀ -aIkenyl, heteroaryl C ^ do-alkyl or heteroaryl-C ₂ -C ₀ alkenyl each having 3 to 5 carbon atoms in the heteroaryl, wherein the C ₁ -C ₀ - or C ₂ -C ₁₀ carbon chain, one or more non-adjacent CH ₂ groups are replaced by oxygen atoms, -N (C ₁ -C ₀ -alkyl) - and / or carbonyl groups can be replaced, and both the phenyl and the heteroaryl having one or more halogen,

CN, R, X-CO-R, XR ^' or CO-XR ^' may be substituted,

R ^{2 is} C ₁ -C ₁₀ -alkyl, C ₂ -C ₀ alkenyl, phenyl, heteroaryl, alkyl having 3 to 5 carbon atoms, phenyl-CrC _10, phenyl-C ₂ -C ₀ alkenyl, heteroaryl Ci-CIO Alkyl or heteroaryl-C ₂ -C ₁₀ alkenyl having in each case 3 to 5 carbon atoms in the heteroaryl radical, wherein in the C ₁ -C ₁₀ - or C ₂ -C ₁₀ carbon chain one or more non-adjacent CH ₂ groups can be replaced by oxygen atoms, -N (C ₁ -C ₁₀ -alkyl) and / or carbonyl groups and both the phenyl and the heteroaryl with one or more halogen, CN, R, CO-R or XR ^' may be substituted

R ¹ ', R ^{2' are} independently of one another hydrogen or independently of R ¹ or R ² the same meaning as R ¹ or R ² ,

R is C ₁ -C ₁₀ -alkyl, C ₂ -C ₁₀ alkenyl, phenyl, heteroaryl atoms having 3 to 5 carbon, phenyl-Ci-C ₁₀ alkyl, phenyl-C ₂ -C ₀ alkenyl, heteroaryl

C ₁ -C ₁₀ -alkyl or heteroaryl C ₂ -C ₁₀ -alkenyl having in each case 3 to 5 carbon atoms in the heteroaryl radical,

R ^'is hydrogen or, independently of R, has the same meaning as R,

X ^{1 is} oxygen or NR ¹ ', where in the event that X ¹ -R ^{1' is} an N (R ^{1 '} ) ₂ -

Group corresponds, the two radicals R ^{1 '} together may form a C ₄ - or C ₅ - alkylene, C ₄ - or C ₅ alkenylene or C ₄ - or C ₅ -Alkadienylenbrücke in which optionally one or two not be - adjacent CH ₂ groups replaced by carbonyl groups and in the case of the alkenylene and Alkadienylenbrücke interconnected by the double bonds carbon atoms may be part of a six-membered aromatic or heteroaromatic ring,

X ² , X are independently of one another oxygen or NR ^{2 '} or NR', where in the event that X ² -R ^{2 '} or XR ^{' is} an N (R ^{2 '} ) ₂ - or N (R ^' ) ₂ - Group corresponds, the two radicals R ² 'and R' together may form a C ₄ - or C ₅ -alkylene or C ₄ - or C ₅ -alkenylene bridge, in which more optionally one or two non-adjacent CH ₂ groups replaced by carbonyl groups and in the case of the alkenylene bridge, the carbon atoms joined together by the double bond may be part of a six-membered aromatic or heteroaromatic ring,

and

n values of 1, 2, 3 or 4,

with the proviso that the total number of aromatic and / or heteroaromatic five- or six-membered rings contained in Ar ^{2 is} a maximum of four. 3. Use of compounds of the formula I according to claim 1, wherein the variables have the following meanings

Ar ^{1 is} an aromatic or heteroaromatic five- or six-membered

Ring substituted with one or more halogen, CN, R ^1, X ¹ -CO-R \ X ¹ - may be substituted R ¹ ', or CO-X ¹ -R ^1',

Ar ^{2 is} an n-valent organic radical which contains one or more aromatic and / or heteroaromatic five- or six-membered rings which are reacted with one or more halogen, CN, R ² , CO-R ² or X ² -R ^{2 '} can be substituted

E -CO-O- or -O-CO-,

R ^1, R ² independently of one another C ₁ -C ₈ -alkyl ₁ is phenyl, heteroaryl having from 3 to 5 carbon atoms, phenyl CRCS alkyl, phenyl-C ₂ -C ₈ alkenyl, heteroaryl-Ci-C ₈ alkyl or heteroaryl-C ₂ -C ₈ -alkenyl each having 3 to 5 carbon atoms in the heteroaryl radical, wherein both the phenyl and the heteroaryl with one or more halogen, CN, R or

X-R 'may be substituted,

R ^{1 '} , R ^{2' are} independently hydrogen or independently of R ¹ or

R ^{2 has} the same meaning as R ¹ or R ² ,

R is C 1 -C 6 -alkyl or phenyl,

R ^'is hydrogen or, independently of R, has the same meaning as R,

X ^{1 is} oxygen or NR ^{1 '} , where in the event that X ¹ -R ¹ ' is an N (R ¹ ') ₂ -

Group corresponds, the two radicals R ¹ 'together may form a C ₄ - or C ₅ - alkylene or C ₄ - or C ₅ alkenylene bridge in which optionally one or two non-adjacent CH ₂ groups may be replaced by carbonyl groups,

X ² , X are independently oxygen or NR ^{2 '} or NR ^' ,

and

n values of 1, 2,

3 or 4, with the proviso that the total number of aromatic and / or heteroaromatic five- or six-membered rings contained in Ar ^{2 is} a maximum of four.

4. Use of compounds of the formula I according to one or more of claims 1 to 3 having a molecular weight of 200 to 2,000 g / mol.

5. Light-emitting layer containing at least one of the compounds of the formula I according to one or more of claims 1 to 4 as a matrix material and at least one further substance distributed therein as an emitter.

6. Light-emitting layer consisting of at least one of the compounds of the formula I according to one or more of claims 1 to 4 as a matrix material and at least one further substance distributed therein as an emitter.

7. Organic light-emitting diode containing a light-emitting layer according to claim 5 or 6.

8. Device selected from the group consisting of stationary screens such as screens of computers, televisions, screens in printers, kitchen appliances and billboards, lighting, signage and mobile screens such as screens in cell phones, laptops, digital cameras, vehicles and destination displays on buses and trains containing one Organic light emitting diode according to claim 7.