Silyl-benzimidazolo[1 ,2-a]benzimidazole as host for Organic Light Emitting Diodes

Description The present invention relates to compounds of formula I and their use in electronic devices, especially electroluminescent devices. When used as hole transport material in electroluminescent devices, the compounds of formula I may provide improved efficiency, stability, manufacturability, or spectral characteristics of electroluminescent devices.

DE102012000064 describes compounds of formula (1 ) and their use in organic light emitting devices (OLEDs). Among others X can be C. If X is C, n i: 1.

WO2012139692 relates to electronic devices which comprise an anode, a cathode and at least one organic layer, where the organic layer comprises one or more substituted ben-

zene com ounds of formula (I), or

(II). Y can be S and n can be 0 or 1 , Z is CR ¹ or N. R ¹ can be an aromatic or hetero aromatic ring system. WO2011/160757 relates to an electronic device comprising an anode, cathode and at least organic layer which contains a compound of formulae

(II), (III), (IV), wherein X may be a single bond and L may be a divalent group. The following 4H-lmidazo[1 ,2-a]imidazole

relates to 4H-lmidazo[1 ,2-a]imidazoles, , such

(A-16), a process for their production and their use in electronic devices, especially electroluminescent devices.

WO2013/050401 describes 4H-imidazo[1 ,2-a]imidazoles of formula

; a process for their production and their use in electronic devices, especially electroluminescent devices.

WO2014/009317 relates to compounds of formula (I), such

as, for example, (B-1 ), a process for their production and their use in electronic devices, especially electroluminescent devices. The 2,5- disubstituted benzimidazo[1 ,2-a]benzimidazole derivatives are suitable hole transporting materials, or host materials for phosphorescent emitters.

WO2014/044722 relates to compounds of formula (I), which are characterized in that they substituted by benzimidazo[1 ,2-a]benzimidazo-5-yl and/or benzimidazo[1 ,2-a]benzimidazo-2,5-ylene groups and in that at least one of the substitu- ents B ¹ , B ² , B ³ , B ⁴ , B ⁵ , B ⁶ , B ⁷ and B ⁸ represents N, a process for their production and their use in electronic devices, especially electroluminescent devices. The compounds of WO2014/044722 may be used host material for phosphorescent emitters in electroluminescent devices.

PCT/EP2014/073038 relates to compounds of formula (I), which are characterized in that they are substituted by benzimidazo[1 ,2-a]benzimidazo-5-yl and/or benzimidazo[1 ,2-a]benzimidazo-2,5-ylene groups and in that at least one of the substitu- ents B ¹ , B ² , B ³ , B ⁴ , B ⁵ , B ⁶ , B ⁷ and B ⁸ represents N ; a process for their production and their use in electronic devices, especially electroluminescent devices.

Notwithstanding these developments, there remains a need for organic light emitting devic- es comprising new hole transport materials to provide improved efficiency, stability, manu- facturability, and/or spectral characteristics of electroluminescent devices.

Accordingly, it is an object of the present invention, with respect to the aforementioned prior art, to provide further materials suitable for use in OLEDs and further applications in organ- ic electronics. More particularly, it should be possible to provide hole transport materials, electron/exciton blocker materials and matrix materials for use in OLEDs. The materials should be suitable especially for OLEDs which comprise at least one phosphorescence emitter, especially at least one green emitter or at least one blue emitter. Furthermore, the materials should be suitable for providing OLEDs which ensure good efficiencies, good operative lifetimes and a high stability to thermal stress, and a low use and operating voltage of the OLEDs.

Said object has been solved by compounds of the formula

(I), wherein

R ¹ , R ² , R ⁴ , R ⁵ , R ⁶ and R ⁷ are independently of each other H, a Ci-C25alkyl group, which can optionally be substituted by E and or interupted by D; or a C2-C6heteroaryl group, which can optionally be su

X ¹ is H, a group of formula

X ² and X ³ are independently of each other H, or a group of formula , or R ²¹ and R ^21' are independently of each other H, a Ci-Cisalkoxy group; a Ci-Cisalkyl group; o roup which is interrupted by -0-, or a group of formula

R ²² , R ² 5, R ²⁶ , R ²⁷ , R ²⁸ , R ² 5', R ² 6', RZT R2ff 25" _i R26", R27", R28", R29, R2ff R29", R40, R43 _anc | R ⁴⁴ and R ⁴⁰ are indepndently of each other H, a Ci-Cisalkoxy group; a Ci-Cisalkyl group; or a Ci-Ci ₈ alkyl group which is interrupted by -0-; D is -CO-, -COO-, -S-, -SO-, -SO2-, -0-, - N R65-, -SiR ⁷⁰ R ⁷¹ -, -POR ⁷² -, -CR ⁶³ =CR ⁶⁴ -, or -C≡C-,

E is -OR ⁶⁹ , -SR ⁶⁹ , -N R65R66, -COR ⁶⁸ , -COOR ⁶⁷ , -CONR ⁶⁵ R ⁶⁶ , -CN, or halogen,

G is E, or a d-dsalkyl group, a phenyl group, a phenyl group, which is substituted by F, Ci-Cisalkyl, or C-i-C-isalkyl which is interrupted by O; a C2-C6heteroaryl group, or a C2- Ceheteroaryl group, which is substituted by F, Ci-Cisalkyl, or C-i-C-isalkyl which is interrupted by O;

R ⁶³ and R ⁶⁴ are independently of each other H, phenyl; phenyl which is substituted by Ci- Ciealkyl, or Ci-Cisalkoxy; C-i-C-isalkyl; or Ci-Cisalkyl which is interrupted by -0-;

R ⁶⁵ and R ⁶⁶ are independently of each other a phenyl group; a phenyl group which is substituted by Ci-Cisalkyl, or C-i-C-isalkoxy; a Ci-Cisalkyl group; or a C-i-C-isalkyl group, which is interrupted by -0-; or

R ⁶⁵ and R ⁶⁶ together form a five or six membered ring,

R ⁶⁷ is a phenyl group; a phenyl group, which is substituted by Ci-Cisalkyl, or C-i-C-isalkoxy; a Ci-Cisalkyl group; or a C-i-C-isalkyl group, which is interrupted by -0-,

R ⁶⁸ is H; a phenyl group; a phenyl group, which is substituted by C-i-C-isalkyl, or Ci- Ciealkoxy; a C-i-C-isalkyl group; or a C-i-C-isalkyl group, which is interrupted by -0-,

R ⁶⁹ is a phenyl group; a C6-Cisaryl group, which is substituted by C-i-C-isalkyl, or C-i- C-isalkoxy; a Ci-Cisalkyl group; or a C-i-C-isalkyl group, which is interrupted by -O-,

R ⁷⁰ and R ⁷¹ are independently of each other a C-i-C-isalkyl group, a phenyl group, or a phenyl group, which is substituted by C-i-C-isalkyl, and

R ⁷² is a Ci-Cisalkyl group, a phenyl group, or a phenyl group, which is substituted by C-i- the proviso that at least one of X ³ is a group of formula

, or comprises a group of formula Certain compounds of the present invention have a HOMO level of 6.0 - 5.7 eV and show, when used as host in combination with phosphorescent emitters, excellent power efficiencies, in particular, electroluminescent (EL) devices comprising the compounds of the present invention exhibit reduced drive voltage while maintaining excellent luminance proper- ties.

The compounds of the present invention have triplet energies of greater than 3.0 eV and, hence, are especially suitable as host for deep blue phosphorescent emitters and in display

applications. Whereas the compound (A-1) of the present i nergy (Ti) of 3.3 eV, the compound of formula

described in US 20070173657 has a Ti of 3.05 eV.

The compounds of the present invention may be used for electrophotographic photoreceptors, photoelectric converters, organic solar cells (organic photovoltaics), switching elements, such as organic transistors, for example, organic FETs and organic TFTs, organic light emitting field effect transistors (OLEFETs), image sensors, dye lasers and electroluminescent devices, such as, for example, organic light-emitting diodes (OLEDs).

Accordingly, a further subject of the present invention is directed to an electronic device, comprising a compound according to the present invention. The electronic device is preferably an electroluminescent device.

The compounds of formula I can in principal be used in any layer of an EL device, but are preferably used as host, hole transport and electron blocking material. Particularly, the compounds of formula I are used as host material for blue light emitting phosphorescent emitters.

Hence, a further subject of the present invention is directed to an hole transport layer, comprising a compound of formula I according to the present invention. A further subject of the present invention is directed to an emitting layer, comprising a compound of formula I according to the present invention. In said embodiment a compound of formula I is preferably used as host material in combination with a phosphorescent emitter. The compounds of formula I have preferably a molecular weight below 1500 g/mol.

A further subject of the present invention is directed to an electron blocking layer, comprising a compound of formula I according to the present invention. The compound of formula (I) is preferably a compound of formula

(la), wherein R ²¹ , R ²² , X ¹ , X ² and X ³ are as defined above.

R ²¹ and R ²² are independently of each other H, a Ci-Cisalkoxy group, a Ci-Cisalkyl group, or a Ci-Cisalkyl group, which is interrupted by -O-.

Compounds of formula (I), especially of formula (la) are preferred, wherein

X ¹ is H, a group of formula , or

X ² and X ³ are independently of each other H, or a group of formula

' are independently of each other H, or a group of formula a group of formula

R ²² is H;

R¾ R26, R27, 28 _i R2ff R26 ¹ . RZT R28 ¹ . R25", R26", R27", R28", R29, R2ff R29", R40, R43 _{a nc} | R44 are independently of each other H, or a Ci-Cisalkyl group, with the proviso that at least one

and X ³ is group of formula and/or

In said embodiment compounds are more referred, Wherein R ² 5, R ² 6, R27, R28, R2ff R26 ¹ . R2T R28 ¹ . R25", R26", R27", R28", R29, R2ff R29 ", R40, R43 _anC | R44 _are H _.

In addition, compounds of formula (I), especially of formula (la) are preferred, wherein

X ¹ is a group of formula , wherein R ²⁵ , R ²⁶ , R27

R28, R25', R26'_ R27'_ R28'_ R29 _anc | R4o _are independently of each other H , or a Ci-Ci ₈ alkyl group, and X ² , X3, R2i , R22 _anc | χ3 _ARE H.

R25, R26, R27, R28, R25 ¹ . R26 ¹ . R2T R2ff R29 _anc | R40 _are preferably H .

In addition, compounds of formula (I), especially of formula (la) are preferred, wherein

X ² is a group of formula , wherein R ²⁵ , R ²⁶ , R ²⁷ ,

R ²⁸ , R ^25' , R ^26' , R ^27' , R ^28' , R ²⁹ and R ⁴⁰ are independently of each other H, or a Ci-Ci ₈ alkyl group, and X ¹ , X ³ , R ²¹ , R ²² and X ³ are H .

R ² 5, R ² 6, R ²⁷ , R ²⁸ , R ² 5', R ² 6', R ^27' , R ^28' , R ²⁹ and R ⁴⁰ are preferably H .

In more preferred embodiments the present invention is directed to compounds of formula 

compounds of formula (lb), or (Ic), wherein

or compounds of formula (lb), or (Ic), wherein

Compounds of formula (lb), or (Ic) are even more preferred, wherein one of the groups X ¹ ,

X ² , or X ³ is a group of formula and the other two groups represent H.

In addition, compounds of formula (lb), or (Ic) are even more preferred, wherein two of the

groups X ¹ , X ² , or X ³ are a group of formula and the other group represent H.

In addition, compounds of formula (lb), or (Ic) are even more preferred, wherein one of the

groups X ¹ , X ² , or X ³ is a group of formula

other two groups represent H.

(A-2), 



Ci-C25alkyl (Ci-Cisalkyl) is typically linear or branched, where possible. Examples are methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert.-butyl, n-pentyl, 2-pentyl, 3- pentyl, 2,2-dimethylpropyl, 1 ,1 ,3,3-tetramethylpentyl, n-hexyl, 1-methylhexyl, 1 ,1 ,3,3,5,5- hexa methyl hexyl, n-heptyl, isoheptyl, 1 ,1 ,3,3-tetramethylbutyl, 1-methylheptyl, 3-methyl- heptyl, n-octyl, 1 ,1 ,3,3-tetramethylbutyl and 2-ethylhexyl, n-nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, or octadecyl. Ci-Ci8alkoxy groups are straight-chain or branched alkoxy groups, e.g. methoxy, ethoxy, n- propoxy, isopropoxy, n-butoxy, sec-butoxy, tert-butoxy, amyloxy, isoamyloxy or tert- amyloxy, heptyloxy, octyloxy, isooctyloxy, nonyloxy, decyloxy, undecyloxy, dodecyloxy, tetradecyloxy, pentadecyloxy, hexadecyloxy, heptadecyloxy and octadecyloxy. Examples of d-Csalkoxy are methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy, tert.-butoxy, n-pentyloxy, 2-pentyloxy, 3-pentyloxy, 2,2-dimethylpropoxy, n-hexyloxy, n- heptyloxy, n-octyloxy, 1 ,1 ,3,3-tetramethylbutoxy and 2-ethylhexyloxy.

Examples of a "C2-C6heteroaryl" group are a imidazoyi group, a 4-(1 ,2,4-triazoyl) group and a 1-(1 ,2,4-triazolyl) group.

G is as defined above and is especially Ci-Cisalkyl, very especially d-Csalkyl, such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, isobutyl, tert-butyl, sec-butyl, hexyl, octyl, or 2- ethyl-hexyl. The wording "substituted by G" means that one, or more, especially one to three substitu- ents G might be present. If a substituent occurs more than one time in a group, it can be different in each occurrence.

As described above, the aforementioned groups may be interrupted by D. Interruptions are of course possible only in the case of groups containing at least 2 carbon atoms connected to one another by single bonds. Ci-Cisalkyl interrupted by one or more units D is, for example, (CH2CH ₂ 0)i-9-R ^x , where R ^x is H or Ci-Cioalkyl or C2-Cioalkanoyl (e.g. CO- CH(C2H ₅ )C ₄ H9), CH ₂ -CH(ORy')-CH ₂ -0-Ry, where Ry is Ci-Ci ₈ alkyl, C ₅ -Ci ₂ cycloalkyl, phenyl, C7-Ci5phenylalkyl, and Ry' embraces the same definitions as Ry or is H;

Ci-C ₈ alkylene-COO-R ^z , e.g. CH ₂ COOR _z , CH(CH ₃ )COOR ^z , C(CH ₃ ) ₂ COOR ^z , where R ^z is H, Ci-Cisalkyl, (CH2CH20)i-9-R ^x , and R ^x embraces the definitions indicated above;

CH ₂ CH ₂ -0-CO-CH=CH ₂ ; CH ₂ CH(OH)CH2-0-CO-C(CH ₃ )=CH2.

The synthesis of is described, for example, in Achour, Reddouane;

Zniber, Rachid, Bulletin des Societes Chimiques Beiges 96 (1987) 787-92.

For the nucleophilic substitution, diiodobenzoles may be used. The introduction of the

group is performed in the presence of a base. Suitable bases are known to those skilled in the art and are preferably selected from the group consisting of alkali metal and alkaline earth metal hydroxides such as NaOH, KOH, Ca(OH)2, alkali metal hydrides such as NaH, KH, alkali metal amides such as NaNh , alkali metal or alkaline earth metal carbonates such as K2CO3 or CS2CO3, and alkali metal alkoxides such as Na- OMe, NaOEt. In addition, mixtures of the aforementioned bases are suitable. Particular preference is given to NaOH, KOH, NaH or K2CO3. Heteroarylation can be effected, for

example, by copper-catalyzed coupling of to a halogenated compound

of the formula (Ullmann reaction).

The N-arylation was, for example, disclosed in H. Gilman and D. A. Shirley, J. Am. Chem. Soc. 66 (1944) 888; D. Li et al., Dyes and Pigments 49 (2001) 181 - 186 and Eur. J. Org. Chem. (2007) 2147-2151. The reaction can be performed in solvent or in a melt. Suitable solvents are, for example, (polar) aprotic solvents such as dimethyl sulfoxide, dimethylfor- mamide, NMP, tridecane or alcohols. The bromination of 5-phenylbenzimidazolo[1 ,2-a]benzimidazole can be carried out in analogy to the bromination of carbazole, which is, for example, described in J. Mater. Chem. 18 (

Other bromination methods are, for example, described in Helvetica Chimica Acta 89 (2006) 1123 and SYNLETT 17 (2006) 2841-2845. 10.206 The iodination of 5-phenylbenzimidazolo[1 ,2-a]benzimidazole can be done as described in

The halogen/metal exchange is done with nBuLi/THF at -78°C, or tBuLi/THF at -78°C. Reference is made to WO2010/079051 , WO201 1073149, Chemical Communications 2013, 49(64), 7108-71 10, J. Org. Chem.; 1962, 27, 1418-1422; J. Org. Chem.; 1961 , 26, 2013- 2014.

A possible synthetic route for compound (A-1) is shown in the reaction scheme below:

The synthesis of (4-diphenylsilylphenyl)-diphenyl-silane is described in J. Polymer Science: part A, 1964, 2, 15-19.

(4-Diphenylsilylphenyl)-diphenyl-silane can be prepated in in analogy to (4- diphenylsilylphenyl)-diphenyl-silane starting from 1 ,3-dibromobenzene and chlo- ro(diphenyl)silane.

[3-(Benzimidazolo[1 ,2-a]benzimidazol-5-yl)phenyl]-[4-[[3-(benzimidazolo[1 ,2- a]benzimidazol-5-yl)phenyl]-diphenyl-silyl]phenyl]-diphenyl- silane (B-1) can be prepared as described in the following scheme.

[4-[Diphenyl-(5-phenylbenzimidazolo[1 ,2-a]b^

phenylbenzimidazolo[1 ,2-a]benzimidazol-2-yl)silane (C-2) can be prepared as described in t

It has been found that the compounds of the formula I are particularly suitable for use in applications in which charge carrier conductivity is required, especially for use in organic electronics applications, for example selected from switching elements such as organic transistors, e.g. organic FETs and organic TFTs, organic solar cells and organic light- emitting diodes (OLEDs), the compounds of the formula I being particularly suitable in OLEDs for use as host material in a light-emitting layer and/or as electron and/or exciton blocker material and/or as hole transport material, especially in combination with a phosphorescence emitter, very especially blue, or green emitting phosphorescence emitters. In the case of use of the inventive compounds of the formula I in OLEDs, OLEDs which have good efficiencies and a long lifetime and which can be operated especially at a low use and operating voltage are obtained. Furthermore, the compounds of the formula I can be used as conductor/complementary materials in organic electronics applications selected from switching elements and organic solar cells.

In the emission layer or one of the emission layers of an OLED, it is also possible to combine an emitter material with a matrix material of the compound of the formula I and a further matrix material which has, for example, a good elctron transport property. This achieves a high quantum efficiency of this emission layer.

Suitable structures of organic electronic devices are known to those skilled in the art and are specified below.

The organic transistor generally includes a semiconductor layer formed from an organic layer with hole transport capacity and/or electron transport capacity; a gate electrode formed from a conductive layer; and an insulating layer introduced between the semiconductor layer and the conductive layer. A source electrode and a drain electrode are mounted on this arrangement in order thus to produce the transistor element. In addition, further layers known to those skilled in the art may be present in the organic transistor.

The organic solar cell (photoelectric conversion element) generally comprises an organic layer present between two plate-type electrodes arranged in parallel. The organic layer may be configured on a comb-type electrode. There is no particular restriction regarding the site of the organic layer and there is no particular restriction regarding the material of the electrodes. When, however, plate-type electrodes arranged in parallel are used, at least one electrode is preferably formed from a transparent electrode, for example an ITO electrode or a fluorine-doped tin oxide electrode. The organic layer is formed from two sublayers, i.e. a layer with p-type semiconductor properties or hole transport capacity, and a layer formed with n-type semiconductor properties or electron transport capacity. In addition, it is possible for further layers known to those skilled in the art to be present in the organic solar cell. The layer with hole transport capacity may comprise the compounds of formula I.

Structure of the inventive OLED

The inventive organic light-emitting diode (OLED) generally has the following structure: an anode (a) and a cathode (i) and a light-emitting layer (e) arranged between the anode (a) and the cathode (i).

The inventive OLED may, for example - in a preferred embodiment - be formed from the following layers:

1. Anode (a)

2. Hole transport layer (c)

3. Light-emitting layer (e)

4. Blocking layer for holes/excitons (f)

5. Electron transport layer (g)

6. Cathode (i) Layer sequences different than the aforementioned structure are also possible, and are known to those skilled in the art. For example, it is possible that the OLED does not have all of the layers mentioned; for example, an OLED with layers (a) (anode), (e) (light-emitting layer) and (i) (cathode) is likewise suitable, in which case the functions of the layers (c) (hole transport layer) and (f) (blocking layer for holes/excitons) and (g) (electron transport layer) are assumed by the adjacent layers. OLEDs which have layers (a), (c), (e) and (i), or layers (a), (e), (f), (g) and (i), are likewise suitable. In addition, the OLEDs may have a blocking layer for electrons/excitons (d) between the hole transport layer (c) and the Light- emitting layer (e). It is additionally possible that a plurality of the aforementioned functions (electron/exciton blocker, hole/exciton blocker, hole injection, hole conduction, electron injection, electron conduction) are combined in one layer and are assumed, for example, by a single material present in this layer. For example, a material used in the hole transport layer, in one embodiment, may simultaneously block excitons and/or electrons. Furthermore, the individual layers of the OLED among those specified above may in turn be formed from two or more layers. For example, the hole transport layer may be formed from a layer into which holes are injected from the electrode, and a layer which transports the holes away from the hole-injecting layer into the light-emitting layer. The electron transport layer may likewise consist of a plurality of layers, for example a layer in which electrons are injected by the electrode, and a layer which receives electrons from the electron injection layer and transports them into the light-emitting layer. These layers mentioned are each selected according to factors such as energy level, thermal resistance and charge carrier mobility, and also energy difference of the layers specified with the organic layers or the metal electrodes. The person skilled in the art is capable of selecting the structure of the OLEDs such that it is matched optimally to the organic compounds used in accordance with the invention.

In a preferred embodiment the OLED according to the present invention comprises in this order:

(a) an anode,

(b) optionally a hole injection layer,

(c) optionally a hole transport layer,

(d) optionally an electron/exciton blocking layer

(e) an emitting layer,

(f) optionally a hole/ exciton blocking layer

(g) optionally an electron transport layer,

(h) optionally an electron injection layer, and

(i) a cathode.

In a particularly preferred embodiment the OLED according to the present invention comprises in this order:

(a) an anode,

(b) optionally a hole injection layer,

(c) a hole transport layer,

(d) an electron/exciton blocking layer

(e) an emitting layer,

(f) a hole/ exciton blocking layer

(g) an electron transport layer, and

(h) optionally an electron injection layer, and

(i) a cathode.

The properties and functions of these various layers, as well as example materials are known from the prior art and are described in more detail below on basis of preferred em- bodiments.

Anode (a):

The anode is an electrode which provides positive charge carriers. It may be composed, for example, of materials which comprise a metal, a mixture of different metals, a metal alloy, a metal oxide or a mixture of different metal oxides. Alternatively, the anode may be a conductive polymer. Suitable metals comprise the metals of groups 11 , 4, 5 and 6 of the Periodic Table of the Elements, and also the transition metals of groups 8 to 10. When the anode is to be transparent, mixed metal oxides of groups 12, 13 and 14 of the Periodic Table of the Elements are generally used, for example indium tin oxide (ITO). It is likewise possible that the anode (a) comprises an organic material, for example polyaniline, as described, for example, in Nature, Vol. 357, pages 477 to 479 (June 11 , 1992). Preferred anode materials include conductive metal oxides, such as indium tin oxide (ITO) and indium zinc oxide (IZO), aluminum zinc oxide (AlZnO), and metals. Anode (and substrate) may be sufficiently transparent to create a bottom-emitting device. A preferred transparent substrate and anode combination is commercially available ITO (anode) deposited on glass or plastic (substrate). A reflective anode may be preferred for some top-emitting devices, to increase the amount of light emitted from the top of the device. At least either the anode or the cathode should be at least partly transparent in order to be able to emit the light formed. Other anode materials and structures may be used.

Hole injection layer (b):

Generally, injection layers are comprised of a material that may improve the injection of charge carriers from one layer, such as an electrode or a charge generating layer, into an adjacent organic layer. Injection layers may also perform a charge transport function. The hole injection layer may be any layer that improves the injection of holes from anode into an adjacent organic layer. A hole injection layer may comprise a solution deposited material, such as a spin-coated polymer, or it may be a vapor deposited small molecule material, such as, for example, CuPc, MTDATA, , or dipyrazino[2,3-f:2',3'-h]quinoxaline- 2,3,6,7,10,11-hexacarbonitrile (HAT-CN). Polymeric hole-injection materials can be used such as poly(N-vinylcarbazole) (PVK), polythiophenes, polypyrrole, polyaniline, self-doping polymers, such as, for example, sulfonated poly(thiophene-3-[2[(2-methoxyethoxy)ethoxy]- 2,5-diyl) (Plexcore ^® OC Conducting Inks commercially available from Plextronics), and copolymers such as poly(3,4-ethylenedioxythiophene)/poly(4-styrenesulfonate) also called PEDOT/PSS. Preferred examples of a material of the hole injecting layer are a porphyrin compound, an aromatic tertiary amine compound, or a styrylamine compound. Particularly preferable examples include an aromatic tertiary amine compound such as hexacyanohex- aazatriphenylene (HAT).

Hole transport layer (c):

Either hole-transporting molecules or polymers may be used as the hole transport material. Suitable hole transport materials for layer (c) of the inventive OLED are disclosed, for example, in Kirk-Othmer Encyclopedia of Chemical Technology, 4th Edition, Vol. 18, pages 837 to 860, 1996, US20070278938, US2008/0106190, US201 1/0163302 (triarylamines with (di)benzothiophen/(di)benzofuran; Nan-Xing Hu et al. Synth. Met. 11 1 (2000) 421 (in- dolocarbazoles), WO2010002850 (substituted phenylamine compounds) and

WO2012/16601 (in particular the hole transport materials mentioned on pages 16 and 17 of WO2012/16601). Combination of different hole transport material may be used. Reference

is m

and (HTL2-1) constitute the hole transport layer.

sisting of

(4-phenyl-N-(4-p -[4-(4-phenyl-

phenyl)phenyl]anilino)phenyl]phenyl]aniline), (4-phenyl-N-(4- (4-phenyl-N-(4-phenylphenyl)anilino)phenyl]phenyl]aniline),

(9-phenylcarbazol-3-yl)phenyl]-N-(4-

phenylphenyl)aniline), (1 ,1',3,3'-tetraphenylspiro[1 ,3,2-benzodiazasilole- 2,2'-3a,7a-dihydro-1 ,3,2-benzodiazasilole]),

(N2,N2,N2',N2',N7,N7,N7',N7'-octakis(p^ 4,4'- bis[N-(1-naphthyl)-N-phenylamino]biphenyl (a-NPD), N,N'-diphenyl-N,N'-bis(3- methylphenyl)-[1 ,1 '-biphenyl]-4,4'-diamine (TPD), 1 ,1-bis[(di-4-tolylamino)phenyl]- cyclohexane (TAPC), N,N'-bis(4-methylphenyl)-N,N'-bis(4-ethylphenyl)-[1 ,1 '-(3,3'-dimethyl)- biphenyl]-4,4'-diamine (ETPD), tetrakis(3-methylphenyl)-N,N,N',N'-2,5-phenylenediamine (PDA), a-phenyl-4-N,N-diphenylaminostyrene (TPS), p-(diethylamino)benzaldehyde diphe- nylhydrazone (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-carbazol9-yl)- cyclobutane (DCZB), N,N,N',N'-tetrakis(4-methylphenyl)-(1 ,1 '-biphenyl)-4,4'-diamine (TTB), fluorine compounds such as 2,2',7,7'-tetra(N,N-di-tolyl)amino9,9-spirobifluorene (spiro- TTB), N,N'-bis(naphthalen-1-yl)-N,N'-bis(phenyl)9,9-spirobifluoren e (spiro-NPB) and 9,9- bis(4-(N,N-bis-biphenyl-4-yl-amino)phenyl-9Hfluorene, benzidine compounds such as Ν,Ν'- bis(naphthalen-1-yl)-N,N'-bis(phenyl)benzidine and porphyrin compounds such as copper phthalocyanines. In addition, polymeric hole-injection materials can be used such as poly(N-vinylcarbazole) (PVK), polythiophenes, polypyrrole, polyaniline, self-doping polymers, such as, for example, sulfonated poly(thiophene-3-[2[(2-methoxyethoxy)ethoxy]-2,5- diyl) (Plexcore® OC Conducting Inks commercially available from Plextronics), and copol- ymers such as poly(3,4-ethylenedioxythiophene)/poly(4-styrenesulfonate) also called PE- DOT/PSS. In addition, dibenz nds mentioned as host

below, such as, for example, (SH-1), may be used as hole transport material and exciton blocker material.

In a preferred embodiment it is possible to use metal carbene complexes as hole transport materials. Suitable carbene complexes are, for example, carbene complexes as described in WO2005/019373A2, WO2006/056418 A2, WO2005/113704, WO2007/1 15970,

WO2007/115981 , WO2008/000727 and WO2014147134. One example of a suitable car-

bene complex is lr(DPBIC)3 with the formula: ³ (HTM-1). Another ex- am rbene complex is lr(ABIC)3 with

la: ³ (HTM-2). In another preferred embodiment compounds of formula (I), especially (la), (lb) and (lc), very especially compounds (A-1 ) to (A-12), (B-1 ), (B-2), (C-1) and (C-2) are used as hole transport material.

The hole-transporting layer may also be electronically doped in order to improve the transport properties of the materials used, in order firstly to make the layer thicknesses more generous (avoidance of pinholes/short circuits) and in order secondly to minimize the operating voltage of the device. Electronic doping is known to those skilled in the art and is disclosed, for example, in W. Gao, A. Kahn, J. Appl. Phys., Vol. 94, 2003, 359 (p-doped organic layers); A. G. Werner, F. Li, K. Harada, M. Pfeiffer, T. Fritz, K. Leo, Appl. Phys. Lett., Vol. 82, No. 25, 2003, 4495 and Pfeiffer et al., Organic Electronics 2003, 4, 89 - 103 and K. Walzer, B. Maennig, M. Pfeiffer, K. Leo, Chem. Soc. Rev. 2007, 107, 1233. For example it is possible to use mixtures in the hole-transporting layer, in particular mixtures which lead to electrical p-doping of the hole-transporting layer. p-Doping is achieved by the addition of oxidizing materials. These mixtures may, for example, be the following mixtures: mixtures of the abovementioned hole transport materials with at least one metal oxide, for example M0O2, M0O3, WO _x , ReCb and/or V2O5, preferably M0O3 and/or ReCb, or mixtures comprising the aforementioned hole transport materials and one or more compounds selected from 7,7,8,8-tetracyanoquinodimethane (TCNQ), 2,3,5,6-tetrafluoro-7,7,8,8- tetracyanoquinodimethane (F4-TCNQ), 2,5-bis(2-hydroxyethoxy)-7,7,8,8- tetracyanoquinodimethane, bis(tetra-n-butylammonium)tetracyanodiphenoquinodimethane, 2,5-dimethyl-7,7,8,8-tetracyanoquinodimethane, tetracyanoethylene, 1 1 ,11 ,12,12- tetracyanonaphtho2,6-quinodimethane, 2-fluoro-7,7,8,8-tetracyanoquino-dimethane, 2,5- difluoro-7,7,8,8etracyanoquinodimethane, dicyanomethylene-1 ,3,4,5,7,8-hexafluoro-6H- naphthalen-2-ylidene)malononitrile (Fe-ΤΝΑΡ), Mo(tfd)3 (from Kahn et al., J. Am. Chem. Soc. 2009, 131 (35), 12530-12531 ), compounds as described in EP1988587,

US2008265216, EP2180029, US20100102709, WO2010132236, EP2180029 and quinone compounds as mentioned in EP2401254. Preferred mixtures comprise the aforementioned carbene complexes, such as, for example, the carbene complexes HTM-1 and HTM-2, and M0O3 and/or ReCb. In a particularly preferred embodiment the hole transport layer comprises from 0.1 to 10 wt % of M0O3 and 90 to 99.9 wt % carbene complex, especially of a carbene complex HTM-1 and HTM-2, wherein the total amount of the M0O3 and the carbene complex is 100 wt %. In another particularly preferred embodiment the hole transport layer comprises from 0.1 to 10 wt % of M0O3 and 90 to 99.9 wt % dibenzofurane compound, especially compound (SH-1), wherein the total amount of the M0O3 and the carbene complex is 100 wt %.

Exciton blocking layer (d):

Blocking layers may be used to reduce the number of charge carriers (electrons or holes) and/or excitons that leave the emissive layer. An electron/exciton blocking layer (d) may be disposed between the first emitting layer (e) and the hole transport layer (c), to block electrons from emitting layer (e) in the direction of hole transport layer (c). Blocking layers may also be used to block excitons from diffusing out of the emissive layer. Suitable metal com- plexes for use as electron/exciton blocker material are, for example, carbene complexes as described in WO2005/019373A2, WO2006/056418A2, WO2005/113704, WO2007/115970, WO2007/115981 , WO2008/000727 and WO2014147134. Explicit reference is made here to the disclosure of the WO applications cited, and these disclosures shall be considered to be incorporated into the content of the present application. One example of a suitable car- bene complex is compound HTM-1. Another example of a suitable carbene complex is compound HTM-2. In addition, all hole transport materials having sufficient high triplet energy are suitable exciton blocking materials. Additional examples of hole transporting materials having sufficient high triplet energy are (SH-1) and (SH-11). In another preferred embodiment compounds of formula (I), especially (la), (lb) and (lc), very especially compounds (A-1 ) to (A-12), (B-1 ), (B-2), (C-1) and (C-2) are used as electron/exciton blocking material.

Emitting layer (e)

The light-emitting layer (e) comprises at least one emitter material. In principle, it may be a fluorescence or phosphorescence emitter, suitable emitter materials being known to those skilled in the art. The at least one emitter material is preferably a phosphorescence emitter. The phosphorescence emitter compounds used with preference are based on metal complexes, and especially the complexes of the metals Ru, Rh, Ir, Pd and Pt, in particular the complexes of Ir, have gained significance. The compounds of the formula I can be used as the matrix in the light-emitting layer.

Suitable metal complexes for use in the inventive OLEDs are described, for example, in documents WO 02/60910 A1 , US 2001/0015432 A1 , US 2001/0019782 A1 ,

US 2002/0055014 A1 , US 2002/0024293 A1 , US 2002/0048689 A1 , EP 1 191 612 A2, EP 1 191 613 A2, EP 1 21 1 257 A2, US 2002/0094453 A1 , WO 02/02714 A2,

WO 00/70655 A2, WO 01/41512 A1 , WO 02/15645 A1 , WO 2005/019373 A2,

WO 2005/113704 A2, WO 2006/1 15301 A1 , WO 2006/067074 A1 , WO 2006/056418, WO 2006121811 A1 , WO 2007095118 A2, WO 2007/115970, WO 2007/115981 ,

WO 2008/000727, WO2010129323, WO2010056669, WO10086089, US2011/0057559, WO2011/106344, US201 1/0233528, WO2012/048266, WO2012/172482, WO2015000955 and PCT/EP2014/066272.

Further suitable metal complexes are the commercially available metal complexes tris(2- phenylpyridine)iridium(lll), iridium(lll) tris(2-(4-tolyl)pyridinato-N,C ² '), bis(2- phenylpyridine)(acetylacetonato)iridium(lll), iridium(lll) tris(l-phenylisoquinoline), iridium(lll) bis(2,2'-benzothienyl)pyridinato-N,C ³ ')(acetylacetonate), tris(2-phenylquinoline)iridium(lll), iridium(lll) bis(2-(4,6-difluorophenyl)pyridinato-N,C ² )picolinate, iridium(lll) bis(1- phenylisoquinoline)(acetylacetonate), bis(2-phenylquinoline)(acetylacetonato)iridium(lll), iridium(lll) bis(di-benzo[f,h]quinoxaline)(acetylacetonate), iridium(lll) bis(2-methyldi- benzo[f,h]quinoxaline)(acetylacetonate) and tris(3-methyl-1-phenyl-4-trimethylacetyl-5- pyrazolino)terbium(lll), bis[1-(9,9-dimethyl-9H-fluoren-2-yl)isoquinoline](acetyl- acetonato)iridium(lll), bis(2-phenylbenzothiazolato)(acetylacetonato)iridium(lll), bis(2-(9,9- dihexylfluorenyl)-1-pyridine)(acetylacetonato)iridium(lll), bis(2-benzo[b]thiophen-2-yl- pyridine)(acetylacetonato)iridium(lll).

In addition, the following commercially available materials are suitable:

tris(dibenzoylacetonato)mono(phenanthroline)europium(lll) , tris(dibenzoylmethane)- mono(phenanthroline)europium(lll), tris(dibenzoylmethane)mono(5-aminophenanthroline)- europium(lll), tris(di-2-naphthoylmethane)mono(phenanthroline)europium(lll) , tris(4- bromobenzoylmethane)mono(phenanthroline)europium(lll), tris(di(biphenyl)methane)- mono(phenanthroline)europium(lll), tris(dibenzoylmethane)mono(4,7-diphenyl- phenanthroline)europium(lll), tris(dibenzoylmethane)mono(4,7-di-methyl- phenanthroline)europium(lll), tris(dibenzoylmethane)mono(4,7-dimethylphenan- throlinedisulfonic acid)europium(lll) disodium salt, tris[di(4-(2-(2-ethoxyethoxy)ethoxy)- benzoylmethane)]mono(phenanthroline)europium(lll) and tris[di[4-(2-(2-ethoxy- ethoxy)ethoxy)benzoylmethane)]mono(5-aminophenanthroline)eur opium(lll), osmium(ll) bis(3-(trifluoromethyl)-5-(4-tert-butylpyridyl)-1 ,2,4-triazolato)diphenylmethylphosphine, os- mium(ll) bis(3-(trifluoromethyl)-5-(2-pyridyl)-1 ,2,4-triazole)dimethylphenylphosphine, osmi- um(ll) bis(3-(trifluoromethyl)-5-(4-tert-butylpyridyl)-1 ,2,4- triazolato)dimethylphenylphosphine, osmium(ll) bis(3-(trifluoromethyl)-5-(2-pyridyl)- pyrazolato)dimethylphenylphosphine, tris[4,4'-di-tert-butyl(2,2')-bipyridine]ruthenium(lll), osmium(ll) bis(2-(9,9-dibutylfluorenyl)-1-isoquinoline(acetylacetonate) . Preferred phosphorescence emitters are carbine complexes. Suitable phosphorescent blue emitters are specified in the following publications: WO2006/056418A2, WO2005/113704, WO2007/115970, WO2007/115981 , WO2008/000727, WO2009050281 , WO2009050290, WO2011051404, US201 1/057559 WO2011/073149, WO2012/121936A2,

US2012/0305894A1 , WO2012/170571 , WO2012/170461 , WO2012/170463,

WO2006/12181 1 , WO2007/095118, WO2008/156879, WO2008/156879, WO2010/068876, US201 1/0057559, WO2011/106344, US2011/0233528, WO2012/048266,

WO2012/172482, WO2015000955 and PCT/EP2014/066272.

Preferably, the light emitting layer (e) comprises at least one carbine complex as phosphorescence emitter. Suitable carbine complexes are, for example, compounds of the formula (IX), which are described in WO 2005/019373 A2, wherein the symbols have the following meanings:

M is a metal atom selected from the group consisting of Co, Rh, Ir, Nb, Pd, Pt, Fe, Ru, Os, Cr, Mo, W, Mn, Tc, Re, Cu, Ag and Au in any oxidation state possible for the respective metal atom;

Carbene is a carbene ligand which may be uncharged or monoanionic and monodentate, bidentate or tridentate, with the carbene ligand also being able to be a biscarbene or triscarbene ligand;

L is a monoanionic or dianionic ligand, which may be monodentate or bidentate;

K is an uncharged monodentate or bidentate ligand selected from the group consisting of phosphines; phosphonates and derivatives thereof, arsenates and derivatives thereof; phosphites; CO; pyridines; nitriles and conjugated dienes which form a π complex with M ¹ ; n1 is the number of carbene ligands, where n1 is at least 1 and when n1 > 1 the carbene ligands in the complex of the formula I can be identical or different;

ml is the number of ligands L, where ml can be 0 or≥ 1 and when ml > 1 the ligands L can be identical or different;

o is the number of ligands K, where o can be 0 or≥ 1 and when o > 1 the ligands K can be identical or different;

where the sum n1 + ml + o is dependent on the oxidation state and coordination number of the metal atom and on the denticity of the ligands carbene, L and K and also on the charge on the ligands, carbene and L, with the proviso that n1 is at least 1. lexes of the general formula

IXa), which are described in WO2011/073149, where M, n1 , Y, A ² ', A3', A A^, Rsi , R52, RSS, R54, RSS, Rse, RS?, RSS, R59, κ, L, ml and o1 are each defined as follows:

M is Ir, or Pt,

n1 is an integer selected from 1 , 2 and 3,

Y is NR ⁵ⁱ , 0, S or C(R2 ⁵ ) ₂ ,

A ^2' , A ^3' , A ^4' , and A ^5' are each independently N or C, where 2 A' = nitrogen atoms and at least one carbon atom is present between two nitrogen atoms in the ring,

R ⁵¹ is a linear or branched alkyl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 1 to 20 carbon atoms, cycloalkyi radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 3 to 20 carbon atoms, substituted or unsubstituted aryl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 6 to 30 carbon atoms, substituted or unsubstituted heteroaryl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having a total of 5 to 18 carbon atoms and/or heteroatoms,

R ⁵² , R ⁵³ , R ⁵⁴ and R ⁵⁵ are each, if A ^2' , A ^3' , A ^4' and/or A ^5' is N, a free electron pair, or, if A ^2' , A ^3' , A ^4' and/or A ^5' is C, each independently hydrogen, linear or branched alkyl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 1 to 20 carbon atoms, cycloalkyl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 3 to 20 carbon atoms, substituted or unsubstituted aryl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 6 to 30 carbon atoms, substituted or unsubstituted heteroaryl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having a total of 5 to 18 carbon atoms and/or heteroatoms, group with donor or acceptor action, or

R ⁵³ and R ⁵⁴ together with A ^3' and A ^4' form an optionally substituted, unsaturated ring optionally interrupted by at least one further heteroatom and having a total of 5 to 18 carbon atoms and/or heteroatoms,

R ⁵⁶ , R ⁵⁷ , R ⁵⁸ and R ⁵⁹ are each independently hydrogen, linear or branched alkyl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 1 to 20 carbon atoms, cycloalkyl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 3 to 20 carbon atoms, cycloheteroalkyl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 3 to 20 carbon atoms, substituted or unsubstituted aryl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 6 to 30 carbon atoms, substituted or unsubstituted heteroaryl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having a total of 5 to 18 carbon atoms and/or heteroatoms, group with donor or acceptor action, or

R ⁵⁶ and R ⁵⁷ , R ⁵⁷ and R ⁵⁸ or R ⁵⁸ and R ⁵⁹ , together with the carbon atoms to which they are bonded, form a saturated, unsaturated or aromatic, optionally substituted ring optionally interrupted by at least one heteroatom and having a total of 5 to 18 carbon atoms and/or heteroatoms, and/or

if A ^5' is C, R ⁵⁵ and R ⁵⁶ together form a saturated or unsaturated, linear or branched bridge optionally comprising heteroatoms, an aromatic unit, heteroaromatic unit and/or functional groups and having a total of 1 to 30 carbon atoms and/or heteroatoms, to which is optionally fused a substituted or unsubstituted, five- to eight-membered ring comprising carbon atoms and/or heteroatoms,

R ²⁵ is independently a linear or branched alkyl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 1 to 20 carbon at- oms, cycloalkyl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 3 to 20 carbon atoms, substituted or unsubstituted aryl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having 6 to 30 carbon atoms, substituted or unsubstituted heteroaryl radical optionally interrupted by at least one heteroatom, optionally bearing at least one functional group and having a total of 5 to 18 carbon atoms and/or heteroatoms, K is an uncharged mono- or bidentate ligand,

L is a mono- or dianionic ligand, preferably monoanionic ligand, which may be mono- bidentate,

ml is 0, 1 or 2, where, when ml is 2, the K ligands may be the same or different, o1 is 0, 1 or 2, where, when o1 is 2, the L ligands may be the same or different.

(BE-9), (BE-10), 32

33





(BE-81), (BE-82),

(BE-107), (BE-108), 40

41

The compound of formula IX is more preferably a compound (BE-1 ), (BE-2), (BE-7), (BE- 12), (BE-16), (BE-64), or (BE-70). The most preferred phosphorescent blue emitters are compounds (BE-1 ) and (BE-12).

The homoleptic metal-carbene complexes may be present in the form of facial or meridional isomers, preference being given to the facial isomers.

Suitable carbene complexes of formula (IX) and their preparation process are, for example, described in WO201 1/073149.

The compounds of the present invention can also be used as host for phosphorescent green emitters. Suitable phosphorescent green emitters are, for example, specified in the following publications: WO2006014599, WO20080220265, WO2009073245, WO2010027583, WO2010028151 , US20110227049, WO201 1090535, WO2012/08881 , WO20100056669, WO20100118029, WO20100244004, WO201 1109042, WO2012166608, US20120292600, EP2551933A1 ; US6687266, US20070190359, US20070190359, US20060008670; WO2006098460, US20110210316, WO 2012053627; US6921915, US20090039776; JP2007123392 and European patent application no. 14180422.9.

Examples of suitable phosphorescent green emitters are shown below: 43

44

(GE-36) (GE-37),

Host (matrix) materials

The light-emitting layer may comprise further components in addition to the emitter material. For example, a fluroescent dye may be present in the light-emitting layer in order to alter the emission color of the emitter material. In addition - in a preferred embodiment - a matrix material can be used. This matrix material may be a polymer, for example poly(N- vinylcarbazole) or polysilane. The matrix material may, however, be a small molecule, for example 4,4'-N,N'-dicarbazolebiphenyl (CDP=CBP) or tertiary aromatic amines, for example TCTA.

In a preferred embodiment compounds of formula (I), especially (la), (lb) and (lc), very especially compounds (A-1 ) to (A-12), (B-1 ), (B-2), (C-1 ) and (C-2) are used as host.

In a preferred embodiment, the light-emitting layer is formed from 2 to 40% by weight, preferably 5 to 35% by weight, of at least one of the aforementioned emitter materials and 60 to 98% by weight, preferably 75 to 95% by weight, of at least one of the aforementioned, or belowmentioned matrix materials - in one embodiment at least one compound of the formula I - where the sum total of the emitter material and of the matrix material adds up to 100% by weight.

Suitable metal complexes for use together with the compounds of the formula I as matrix material in OLEDs are, for example, also carbene complexes as described in

WO 2005/019373 A2, WO 2006/056418 A2, WO 2005/1 13704, WO 2007/115970,

WO 2007/115981 and WO 2008/000727.

Further suitable host materials, which may be small molecules or (co)polymers of the small molecules mentioned, are specified in the following publications: WO2007108459 (H-1 to H-37), preferably H-20 to H-22 and H-32 to H-37, most preferably H-20, H-32, H-36, H-37, WO2008035571 A1 (Host 1 to Host 6), JP2010135467 (compounds 1 to 46 and Host-1 to Host-39 and Host-43), WO2009008100 compounds No.1 to No.67, preferably No.3, No.4, No.7 to No. 12, No.55, No.59, No. 63 to No.67, more preferably No. 4, No. 8 to No. 12, No. 55, No. 59, No.64, No.65, and No. 67, WO2009008099 compounds No. 1 to No. 110, WO20081401 14 compounds 1-1 to 1-50, WO2008090912 compounds OC-7 to OC-36 and the polymers of Mo-42 to Mo-51 , JP2008084913 H-1 to H-70, WO2007077810 compounds 1 to 44, preferably 1 , 2, 4-6, 8, 19-22, 26, 28-30, 32, 36, 39-44, WO201001830 the polymers of monomers 1-1 to 1-9, preferably of 1-3, 1-7, and 1-9, WO2008029729 the (polymers of) compounds 1-1 to 1-36, WO20100443342 HS-1 to HS-101 and BH-1 to BH-17, preferably BH-1 to BH-17, JP2009182298 the (co)polymers based on the monomers 1 to 75, JP2009170764, JP2009135183 the (co)polymers based on the monomers 1-14, WO2009063757 preferably the (co)polymers based on the monomers 1-1 to 1-26, WO2008146838 the compounds a-1 to a-43 and 1-1 to 1-46, JP2008207520 the

(co)polymers based on the monomers 1-1 to 1-26, JP2008066569 the (co)polymers based on the monomers 1-1 to 1-16, WO2008029652 the (co)polymers based on the monomers 1-1 to 1-52, WO2007114244 the (co)polymers based on the monomers 1-1 to 1-18, JP2010040830 the compounds HA-1 to HA-20, HB-1 to HB-16, HC-1 to HC-23 and the (co)polymers based on the monomers HD-1 to HD-12, JP2009021336, WO2010090077 the compounds 1 to 55, WO2010079678 the compounds H1 to H42, WO2010067746,

WO2010044342 the compounds HS-1 to HS-101 and Poly-1 to Poly-4, JP20101 14180 the compounds PH-1 to PH-36, US2009284138 the compounds 1 to 11 1 and H1 to H71 , WO2008072596 the compounds 1 to 45, JP2010021336 the compounds H-1 to H-38, preferably H-1 , WO2010004877 the compounds H-1 to H-60, JP2009267255 the compounds 1-1 to 1-105, WO2009104488 the compounds 1-1 to 1-38, WO2009086028,

US2009153034, US2009134784, WO2009084413 the compounds 2-1 to 2-56,

JP20091 14369 the compounds 2-1 to 2-40, JP2009114370 the compounds 1 to 67, WO2009060742 the compounds 2-1 to 2-56, WO2009060757 the compounds 1-1 to 1-76, WO2009060780 the compounds 1-1 to 1-70, WO2009060779 the compounds 1-1 to 1-42, WO2008156105 the compounds 1 to 54, JP2009059767 the compounds 1 to 20,

JP2008074939 the compounds 1 to 256, JP2008021687 the compounds 1 to 50,

WO20071 19816 the compounds 1 to 37, WO2010087222 the compounds H-1 to H-31 , WO2010095564 the compounds HOST-1 to HOST-61 , WO2007108362, WO2009003898, WO2009003919, WO2010040777, US2007224446, WO06128800, WO2012014621 , WO2012105310, WO2012/130709, WO2014/009317 (in particular compound A-24), PCT/EP2013/069403 and PCT/EP2013/073120 (in particular page 25 to 29 of

PCT/EP2013/073120).

The above-mentioned small molecules are more preferred than the above-mentioned (co)polymers of the small molecules. xample,

; best results are

achieved if said compounds are combined with );

In a particularly preferred embodiment, one or more compounds of the general formula (X) specified hereina

X is NR, S, O or PR;

R is aryl, heteroaryl, alkyl, cycloalkyi, or heterocycloalkyi;

A200 j _s .N R206R207, _p(O)R208R209 _pR210 211 _ -S(0) ₂ R ²¹² , -S(0)R ²¹³ , -SR214 ₀ ΐ -OR215;

R221 R222 _anc | R223 _are independently of each other aryl, heteroaryl, alkyl, cycloalkyi, or heterocycloalkyi, wherein at least on of the groups R ²²¹ , R ²²² , or R ²²³ is aryl, or heteroaryl; R ²²⁴ and R ²²⁵ are independently of each other alkyl, cycloalkyl, heterocycloalkyi, aryl, heteroaryl, a group A ²⁰⁰ , or a group having donor, or acceptor characteristics;

n2 and m2 are independently of each other 0, 1 , 2, or 3;

R ²⁰⁶ and R ²⁰⁷ form together with the nitrogen atom a cyclic residue having 3 to 10 ring at- oms, which can be unsubstituted, or which can be substituted with one, or more substitu- ents selected from alkyl, cycloalkyl, heterocycloalkyi, aryl, heteroaryl and a group having donor, or acceptor characteristics; and/or which can be annulated with one, or more further cyclic residues having 3 to 10 ring atoms, wherein the annulated residues can be unsubstituted, or can be substituted with one, or more substituents selected from alkyl, cycloalkyl, heterocycloalkyi, aryl, heteroaryl and a group having donor, or acceptor characteristics; and R208 _i R209 _i R2io_ 2i i _ 212_ 213_ R214 _{u nc} | R215 _are independently of each other aryl, het, for exam-

(SH-5), or

(SH-6), are described in WO2010079051 (in particular pages on 19 to 26 and in tables on pages 27 to 34, pages 35 to 37 and pages 42 to 43).

Additional host materials on basis of dibenzofurane are, for example, described in

US2009066226, EP1885818B1 , EP1970976, EP1998388 and EP2034538. Examples of particularly preferred host materials are shown below:

50

51

In the above-mentioned compounds T is O, or S, preferably O. If T occurs more than one time in a molecule, all groups T have the same meaning. Compounds (SH-1),

most preferred. Hole/exciton blocking layer (f):

Blocking layers may be used to reduce the number of charge carriers (electrons or holes) and/or excitons that leave the emissive layer. The hole blocking layer may be disposed between the emitting layer (e) and electron transport layer (g), to block holes from leaving layer (e) in the direction of electron transport layer (g). Blocking layers may also be used to block excitons from diffusing out of the emissive layer.

Hole blocker materials typically used in OLEDs are 2,6-bis(N-carbazolyl)pyridine (mCPy), 2,9-dimethyl-4,7-diphenyl-1 ,10-phenanthroline (bathocuproin, (BCP)), bis(2-methyl-8- quinolinato)-4-phenylphenylato)aluminum(lll) (BAIq), phenothiazine S,S-dioxide derivates and 1 ,3,5-tris(N-phenyl-2-benzylimidazolyl)benzene) (TPBI), TPBI also being suitable as electron-transport material. Further suitable hole blockers and/or electron conductor materials are 2,2',2"-(1 ,3,5-benzenetriyl)tris(1-phenyl-1-H-benzimidazole), 2-(4-biphenylyl)-5-(4- tert-butylphenyl)-1 ,3,4-oxadiazole, 8-hydroxyquinolinolatolithium, 4-(naphthalen-1-yl)-3,5- diphenyl-4H-1 ,2,4-triazole, 1 ,3-bis[2-(2,2'-bipyridin-6-yl)-1 ,3,4-oxadiazo-5-yl]benzene, 4,7- diphenyl-1 , 10-phenanthroline, 3-(4-biphenylyl)-4-phenyl-5-tert-butylphenyl-1 ,2,4-triazole, 6,6'-bis[5-(biphenyl-4-yl)-1 ,3,4-oxadiazo-2-yl]-2,2'-bipyridyl, 2-phenyl-9,10-di(naphthalene- 2-yl)anthracene, 2,7-bis[2-(2,2'-bipyridin-6-yl)-1 ,3,4-oxadiazo-5-yl]-9,9-dimethylfluorene, 1 ,3-bis[2-(4-tert-butylphenyl)-1 ,3,4-oxadiazo-5-yl]benzene, 2-(naphthalene-2-yl)-4,7- diphenyl-1 , 10-phenanthroline, tris(2,4,6-trimethyl-3-(pyridin-3-yl)phenyl)borane, 2,9- bis(naphthalene-2-yl)-4,7-diphenyl-1 , 10-phenanthroline, 1-methyl-2-(4-(naphthalene-2- yl)phenyl)-1 H-imidazo[4,5-f][1 ,10]phenanthroline. In a further embodiment, it is possible to use compounds which comprise aromatic or heteroaromatic rings joined via groups comprising carbonyl groups, as disclosed in WO2006/100298, disilyl compounds selected from the group consisting of disilylcarbazoles, disilylbenzofurans, disilylbenzothiophenes, dis- ilylbenzophospholes, disilylbenzothiophene S-oxides and disilylbenzothiophene S,S- dioxides, as specified, for example, in PCT applications WO2009/003919 and

WO2009003898 and disilyl compounds as disclosed in WO2008/034758, as a blocking layer for holes/excitons (f). In another preferred embodiment compounds (SH-1 ), (SH-2), (SH-3), (SH-4), (SH-5), (SH- 6), (SH-7), (SH-8), (SH-9), (SH-10) and (SH-11 ) may be used as hole/exciton blocking materials. Electron transport layer (g):

Electron transport layer may include a material capable of transporting electrons. Electron transport layer may be intrinsic (undoped), or doped. Doping may be used to enhance conductivity. Suitable electron-transporting materials for layer (g) of the inventive OLEDs comprise metals chelated with oxinoid compounds, such as tris(8- hydroxyquinolato)aluminum (Alq3), compounds based on phenanthroline such as 2,9- dimethyl-4,7-diphenyl-1 ,10-phenanthroline (DDPA = BCP), 4,7-diphenyl-1 ,10- phenanthroline (Bphen), 2,4,7,9-tetraphenyl-1 ,10-phenanthroline, 4,7-diphenyl-1 ,10- phenanthroline (DPA) or phenanthroline derivatives disclosed in EP1786050, in

EP1970371 , or in EP1097981 , and azole compounds such as 2-(4-biphenylyl)-5-(4-t- butylphenyl)-1 ,3,4-oxadiazole (PBD) and 3-(4-biphenylyl)-4phenyl-5-(4-t-butylphenyl)-1 ,2,4- triazole (TAZ).

It is likewise possible to use mixtures of at least two materials in the electron-transporting layer, in which case at least one material is electron-conducting. Preferably, in such mixed electron-transport layers, at least one phenanthroline compound is used, preferably BCP, or at least one pyridine compound according to the formula (VIII) below, preferably a compound of the formula (Vlllaa) below. More preferably, in mixed electron-transport layers, in addition to at least one phenanthroline compound, alkaline earth metal or alkali metal hy- droxyquinolate complexes, for example Liq, are used. Suitable alkaline earth metal or alkali metal hydroxyquinolate complexes are specified below (formula VII). Reference is made to WO2011/157779.

The electron-transport layer may also be electronically doped in order to improve the transport properties of the materials used, in order firstly to make the layer thicknesses more generous (avoidance of pinholes/short circuits) and in order secondly to minimize the operating voltage of the device. Electronic doping is known to those skilled in the art and is disclosed, for example, in W. Gao, A. Kahn, J. Appl. Phys., Vol. 94, No. 1 , 1 July 2003 (p- doped organic layers); A. G. 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 and K. Walzer, B. Maennig, M. Pfeiffer, K. Leo, Chem. Soc. Rev. 2007, 107, 1233. For example, it is possible to use mixtures which lead to electrical n-doping of the electron- transport layer. n-Doping is achieved by the addition of reducing materials. These mixtures may, for example, be mixtures of the abovementioned electron transport materials with alkali/alkaline earth metals or alkali/alkaline earth metal salts, for example Li, Cs, Ca, Sr, CS2CO3, with alkali metal complexes and with Y, Ce, Sm, Gd, Tb, Er, Tm, Yb, L13N ,

Rb2C03, dipotassium phthalate, W(hpp)4 from EP1786050, or with compounds described in EP1837926B1 , EP1837927, EP2246862 and WO2010132236.

In a preferred embodiment, the electron-transport layer comprises at least one compound of the general formula (VII) , in which

R ³² and R ³³ are each independently F, d-Cs-alkyl, or C6-Ci ₄ -aryl, which is optionally substituted by one or more d-Cs-alkyl groups, or

two R ³² and/or R ³³ substituents together form a fused benzene ring which is optionally substituted by one or more d-Cs-alkyl groups;

a and b are each independently 0, or 1 , 2 or 3,

M ¹ is an alkaline metal atom or alkaline earth metal atom,

p is 1 when M ¹ is an alkali metal atom, p is 2 when M ¹ is an earth alkali metal atom.

A very particularly preferred compound of the formula (VII) is (Liq), which may be present as a single species, or in other forms such as Li _g Q _g in which g is an integer, for example LkQe- Q is an 8-hydroxyquinolate ligand or an 8-hydroxyquinolate derivative.

In a further preferred embodiment, the electron-transport layer comprises at least one compound of the formul

(VIII), in which

R ³⁴ , R ³⁵ , R ³⁶ , R ³⁷ , R ^34' , R ³ 5', RS6' and R ^37' are each independently H , Ci-Cie-alkyl, Ci-Cie- alkyl which is substituted by E and/or interrupted by D, C6-C2 ₄ -aryl, C6-C2 ₄ -aryl which is substituted by G, C2-C2o-heteroaryl or C2-C2o-heteroaryl which is substituted by G, Q is an arylene or heteroarylene group, each of which is optionally substituted by G;

D is -CO-; -COO-; -S-; -SO-; -SO2-; -0-; -N R140-; -SiR ⁴⁵ R ¹⁴⁶ -; -POR ⁴⁷ -; -CR ³⁸ =CR ³⁹ -; or - C≡C-; E is -OR ¹⁴⁴ ; -SR ⁴⁴ ; -N RuoR ; -COR ¹⁴³ ; -COOR ¹⁴² ; -CON Ri ⁴ 0Ri ⁴ i ; -CN; or F; G is E, Ci-Cie-alkyl, Ci-Cie-alkyl which is interrupted by D, Ci-Ci8-perfluoroalkyl, C1-C18- alkoxy, or Ci-Cis-alkoxy which is substituted by E and/or interrupted by D, in which R ³⁸ and R ³⁹ are each independently H , C6-Cie-aryl; C6-Cis-aryl which is substituted by Ci-Cie-alkyl or Ci-Cis-alkoxy; Ci-Cie-alkyl; or Ci-Cie-alkyl which is interrupted by -0-; R ¹⁴⁰ and R ¹⁴¹ are each independently C6-Cie-aryl; C6-Cis-aryl which is substituted by Ci-Cie-alkyl or Ci-Cis-alkoxy; Ci-Cie-alkyl; or Ci-Cie-alkyl which is interrupted by -0-; or R ¹⁴⁰ and R ¹⁴¹ together form a 6-membered ring;

R ¹⁴² and R ¹⁴³ are each independently C6-Cie-aryl; C6-Cis-aryl which is substituted by Ci-Cie-alkyl or Ci-Cis-alkoxy; Ci-Cie-alkyl; or Ci-Cie-alkyl which is interrupted by -0-, R ¹⁴⁴ is C6-Ci8-aryl; C6-Cis-aryl which is substituted by Ci-Cis-alkyl or Ci-Cis-alkoxy; d-C-ιε alkyl; or Ci-Cis-alkyl which is interrupted by -0-,

R ¹⁴⁵ and R ¹⁴⁶ are each independently Ci-Cis-alkyl, C6-Cis-aryl or C6-Cis-aryl which is substituted by Ci-Cis-alkyl,

R ¹⁴⁷ is Ci-Cis-alkyl, C6-Cis-aryl or C6-Cis-aryl which is substituted by Ci-Cis-alkyl.

Preferred compounds of the formula (VIII) are compounds of the formula (Villa)

in which Q is:

R ⁴⁸ is H or Ci-Cis-alkyl and

R ⁴⁸ ' is H , Ci-Cis-alkyl or or

In a further, very particularly preferred embodiment, the electron-transport layer comprises a compound Liq and a compound ETM-2.

In a preferred embodiment, the electron-transport layer comprises the compound of the formula (VII) in an amount of 99 to 1 % by weight, preferably 75 to 25% by weight, more preferably about 50% by weight, where the amount of the compounds of the formulae (VII) and the amount of the compounds of the formulae (VIII) adds up to a total of 100% by weight. The preparation of the compounds of the formula (VIII) is described in J. Kido et al., Chem. Commun. (2008) 5821-5823, J. Kido et al., Chem. Mater. 20 (2008) 5951-5953 and JP2008/127326, or the compounds can be prepared analogously to the processes disclosed in the aforementioned documents. It is likewise possible to use mixtures of alkali metal hydroxyquinolate complexes, preferably Liq, and dibenzofuran compounds in the electron-transport layer. Reference is made to WO2011/157790. Dibenzofuran compounds A-1 to A-36 and B-1 to B-22 described in WO2011/157790 are preferred, wherein dibenzofuran compound

(A-10; = ETM-1) is most preferred.

In a preferred embodiment, the electron-transport layer comprises Liq in an amount of 99 to 1 % by weight, preferably 75 to 25% by weight, more preferably about 50% by weight, where the amount of Liq and the amount of the dibenzofuran compound(s), especially ETM-1 , adds up to a total of 100% by weight.

In a preferred embodiment, the electron-transport layer comprises at least one phenanthro- line derivative and/or pyridine derivative.

In a further preferred embodiment, the electron-transport layer comprises at least one phe- nanthroline derivative and/or pyridine derivative and at least one alkali metal hydroxyquinolate complex.

In a further preferred embodiment, the electron-transport layer comprises at least one of the dibenzofuran compounds A-1 to A-36 and B-1 to B-22 described in WO2011/157790, especially ETM-1.

In a further preferred embodiment, the electron-transport layer comprises a compound described in WO2012/11 1462, WO2012/147397, WO2012014621 , such as, for example, a

compound of formula (ETM-3), US2012/0261654, such as, for example, a compound of

Electron injection layer (h):

The electron injection layer may be any layer that improves the injection of electrons into an adjacent organic layer. Lithium-comprising organometallic compounds such as 8- hydroxyquinolatolithium (Liq), CsF, NaF, KF, CS2CO3 or LiF may be applied between the electron transport layer (g) and the cathode (i) as an electron injection layer (h) in order to reduce the operating voltage.

Cathode (i):

The cathode (i) is an electrode which serves to introduce electrons or negative charge carriers. The cathode may be any metal or nonmetal which has a lower work function than the anode. Suitable materials for the cathode are selected from the group consisting of alkali metals of group 1 , for example Li, Cs, alkaline earth metals of group 2, metals of group 12 of the Periodic Table of the Elements, comprising the rare earth metals and the lanthanides and actinides. In addition, metals such as aluminum, indium, calcium, barium, samarium and magnesium, and combinations thereof, may be used.

In general, the different layers, if present, have the following thicknesses:

anode (a): 500 to 5000 A (angstrom), preferably 1000 to 2000 A;

hole injection layer (b): 50 to 1000 A, preferably 200 to 800 A,

hole-transport layer (c): 50 to 1000 A, preferably 100 to 800 A,

electron/exciton blocking layer (d): 10 to 500 A, preferably 50 to 100 A,

light-emitting layer (e): 10 to 1000 A, preferably 50 to 600 A,

hole/ exciton blocking layer (f): 10 to 500 A, preferably 50 to 100 A,

electron-transport layer (g): 50 to 1000 A, preferably 200 to 800 A,

electron injection layer (h): 10 to 500 A, preferably 20 to 100 A,

cathode (i): 200 to 10 000 A, preferably 300 to 5000 A. The person skilled in the art is aware (for example on the basis of electrochemical studies) of how suitable materials have to be selected. Suitable materials for the individual layers are known to those skilled in the art and are disclosed, for example, in WO 00/70655.

In addition, it is possible that some of the layers used in the inventive OLED have been surface-treated in order to increase the efficiency of charge carrier transport. The selection of the materials for each of the layers mentioned is preferably determined by obtaining an OLED with a high efficiency and lifetime.

The inventive OLED can be produced by methods known to those skilled in the art. In general, the inventive OLED is produced by successive vapor deposition of the individual layers onto a suitable substrate. Suitable substrates are, for example, glass, inorganic semiconductors or polymer films. For vapor deposition, it is possible to use customary tech- niques, such as thermal evaporation, chemical vapor deposition (CVD), physical vapor deposition (PVD) and others. In an alternative process, the organic layers of the OLED can be applied from solutions or dispersions in suitable solvents, employing coating techniques known to those skilled in the art. Use of the compounds of the formula I in at least one layer of the OLED, preferably in the light-emitting layer (preferably as a matrix material), charge transport layer and/or in the charge/exciton blocking layer makes it possible to obtain OLEDs with high efficiency and with low use and operating voltage. Frequently, the OLEDs obtained by the use of the compounds of the formula I additionally have high lifetimes. The efficiency of the OLEDs can additionally be improved by optimizing the other layers of the OLEDs. For example, high-efficiency cathodes such as Ca or Ba, if appropriate in combination with an intermediate layer of LiF, can be used. Moreover, additional layers may be present in the OLEDs in order to adjust the energy level of the different layers and to facilitate electroluminescence. The OLEDs may further comprise at least one second light-emitting layer. The overall emission of the OLEDs may be composed of the emission of the at least two light-emitting layers and may also comprise white light.

The OLEDs can be used in all apparatus in which electroluminescence is useful. Suitable devices are preferably selected from stationary and mobile visual display units and illumination units. Stationary visual display units are, for example, visual display units of computers, televisions, visual display units in printers, kitchen appliances and advertising panels, illuminations and information panels. Mobile visual display units are, for example, visual display units in cellphones, tablet PCs, laptops, digital cameras, MP3 players, vehicles and destination displays on buses and trains. Further devices in which the inventive OLEDs can be used are, for example, keyboards; items of clothing; furniture; wallpaper. In addition, the present invention relates to a device selected from the group consisting of stationary visual display units such as visual display units of computers, televisions, visual display units in printers, kitchen appliances and advertising panels, illuminations, information panels, and mobile visual display units such as visual display units in cellphones, tablet PCs, laptops, digital cameras, MP3 players, vehicles and destination displays on buses and trains; illumination units; keyboards; items of clothing; furniture; wallpaper, comprising at least one inventive organic light-emitting diode or at least one inventive light-emitting layer. The following examples are included for illustrative purposes only and do not limit the scope of the claims. Unless otherwise stated, all parts and percentages are by weight.

Examples

a) 1.00 g (3.53 mmol) 5-phenylbenzimidazolo[1 ,2-a]benzimidazole (example 2a) and 850 mg (2.65 mmol) diacetoxy-iodobenzene in 10 ml acetic acid and 10 ml acetic acid anhydride are heated to 60 °C and then cooled to 25 °C. 340 mg (1.34 mmol) iodine are added. 10 drops of sulfuric acid are added and the reaction mixture is stireed under nitrogen at 25 °C for 18 h. The product is filtered off and is washed with acetic acid, ethanol, water and again ethanol. The product is decocted with methyl ethyl ketone (yield: 560 mg (40 %)). 1 H NMR (400 MHz, THF-d8): δ = 8.39 (d, J= 1.6 Hz, 1 H), 8.1 1-8.14 (m, 1 H), 7.97-8.00 (m, 2H), 7.61-7.71 (m, 4H), 7.37-7.48 (m, 4H). MS (APCI(pos), m/z): 444 (M ⁺ i), 442 (M ⁺ i), 441 (

b) To 5.00 g (12.2 mmol) 2-iodo-5-phenyl-benzimidazolo[1 ,2-a]benzimidazole, 4.77 g (18.3 mmol) triphenylsilane, 5.19 g (24.4 mmol) potassium phosphate in 150 ml dimethylforma- mide is degassed with argon. 160 mg (0.37 mmol) Rhodium(ll)-acetate is added and the reaction mixture is degassed with argon. The reaction mixture is stirred at 60 °C for 5 h under argon. Reaction mixture is poured in water and the water phase is extracted with dichloromethane. The organic phase is washed with 1 % KCN solution in water. The organic phase is dried with magnesium sulfate. The organic phase is filtered on Hyflo. The solvent is distilled off. Product is filtered off and is washed with ethanol. The product is decocted with methyl ethyl ketone. Yield 5.55 g (84 %)

H NMR (400 MHz, DMSO-d6): δ = 8.18 (s, 1 H), 7.91-7.93 (m, 2H), 7.85-7.87 (m, 1 H), 7.67-7.72 (m, 3H), 7.58-7.64 (m, 7H), 7.45-7.54 (m, 10 H), 7.37-7.41 (m, 3H)

Example 2

a) 31.7 g (96.1 mmol) diiodobenzene, 14.9 g (72.1 mmol) 6H-benzimidazolo[1 ,2- a]benzimidazole, 23.5 g (72.1 mmol) cesium carbonate, 1.83 g (9.61 mmol) cupper (I) iodide, 2.21 g (19.3 mmol) L-proline in 400 ml DMSO was stirred under nitrogen at 100 °C for 3 h. The reaction mixture was poured in 600 ml water and the product was filtered off. The product is washed with water and ethanol. 100 ml diethyl ether is added and the mixture is stirred for 3 h. Product is filtered off and is washed with ether. To the product 200 ml dichloromethane is added and the mixture is refluxed for 2 h. The mixture is filtered and washed with dichloromethane. The solvent of the filtrate is distilled off. Colum chromatog- raphy on silica gel with toluene/ethyl acetate 19/1 gave the product 6.47 g (22 %).

1 H NMR (400 MHz, DMSO-d6): δ = 8.32 (t, J =1.8 Hz, 1 H), 8.19-8.24 (m, 2H), 7.93-7.96 (m, 1 -7.88 (m, 1 H), 7.63-7.68 (m 2H), 7.38-7.49 (m, 3H), 7.28-7.36 (m, 2H).

b) 5.00 g (12.2 mmol) 5-(3-iodophenyl)benzimidazolo[1 ,2-a]benzimidazole, 4.77 g (18.3 mmol) triphenylsilane, 3.53 g (16.5 mmol) potassium phosphate in 100 ml dimethylformamide is degassed with argon. 160 mg (0.37 mmol) Rhodium(ll)-acetate is added and the reaction mixture is degassed with argon. The reaction mixture is stirred at 60 °C for 5 h under argon. Reaction mixture is poured in water and the water phase is extracted with dichloromethane. The organic phase is washed with 1 % KCN solution in wa- ter. The organic phase is dried with magnesium sulfate. The organic phase is filtered on silica gel and Hyflo with dichloromethane. The solvent is distilled off. 50 ml diethyl ether is added and the crystalized product is filtered of. The product is soxhlet extracted with methyl ethyl ketone.

Yield 3.31 g (50 %)

H NMR (400 MHz, DMSO-d6): δ = 8.18 (t, J = 8.2 Hz, 2H), 8.09-8.12 (m, 1 H), 7.97-7.98 (m, 1 H), 7.74-7.79 (m, 1 H), 7.58-7.64 (m, 8H), 7.25-7.54 (m, 14 H). MS (APCI(pos), m/z): 542 (M ⁺ i).

Example 3

The synthesis of (4-diphenylsilylphenyl)-diphenyl-silane is described in J. Polymer Science: part A, 1964, 2, 15-19.

a) 5.67 g (25.9 mmol) chloro(diphenyl)silane and 540 mg (22.3 mmol) magnesium are placed under argon in 3 ml water free THF. To this mixture 2.50 g (10.6 mmol) 1 ,4- dibromobenzene are added in a way that the reaction mixture keeps boiling. After adding the 1 ,4-dibromobenzene the reaction mixture is refluxed for 1.5 h.

The reaction mixture is poured into ice water and the water phase is extracted with diethyl ether. The organic phase is dried with magnesium sulfate and the solvent is distilled off. The product is decocted in ethanol and is than crystalized from diethyl ether (yield 3.83 g (82 %)).

b) 970 mg (23.7 mmol) 5-(3-iodophenyl)benzimidazolo[1 ,2-a]benzimidazole (example 2 A) 500 mg (1 .13 mmol) (4-diphenylsilylphenyl)-diphenyl-silane (example 3a)), 480 mg g (2.26 mmol) potassium phosphate tribasic in 25 ml dimethylformamide are degassed with argon. 15 mg (0.03 mmol) Rhodium(ll)-acetate is added, the reaction mixture is degassed with argon, stirred at 60 °C for 5 h under argon and poured into water. The water phase is extracted with dichloromethane. The organic phase is washed with 1 % KCN solution in water. The organic phase is dried with magnesium sulfate. The organic phase is filtered on silica gel and Hyflo with dichloromethane. The solvent is distilled off. The crystalized product is washed with ethanol. The product is crystalized from methyl ethyl ketone (yield 460 mg (40 %)). MS (APCI(pos), m/z): 1005 (M ⁺ⁱ ).

Application Example 1

Determination of triplet energy

The triplet energies of the materials are directly determined from the onsets of the ured phosphorescence spectra of the thin films of neat materials.

imL dichloromethane and second doctor-blading the solutions onto cleaned quartz-slides with a thin film applicator of 30 μιτι slot width (Erichsen, Model 360 02082). For measurement the resulting thin film samples are inserted into a liquid-helium cryostat Optistat CF (Oxford Instruments) and cooled to a temperature of 4-5K. The phosphorescence spectra are measured with a fluorescence/phosphorescence spectrometer FLS- 920P (Edinburgh Instruments). The samples are excited with an electrically pulsed LED model UVTOP 315-HL-T039 (Fa. Roithner, Vienna) with center wavelength 320 nm and pulse widths 5 \is). The emission spectra are detected via time-gated spectroscopy with a delay-time of 26

For compound (A-8), the compound is deposited by vapor deposition to the quartz substrates at a rate of approx. 0.5-5 nm/min at about 10- ⁶ mbar until approx. 60 nm thick film is formed. The results are shown in Table 1 below.

Onset of the neat film gated emission spectrum at 4 K

Compounds (A-8) and (A-1 ) of the present invention have larger triplet energy than the reference compound (SH-1 ).

Comparative Example 1

The ITO substrate used as the anode is first cleaned with isopropanol mixture in an ultrasonic bath. To eliminate any possible organic residues, the substrate is exposed to a continuous ozone flow in an ozone oven for further 25 minutes. This treatment also improves the hole injection properties of the ITO. Then Plexcore ^® OC AJ20-1000 (commercially available from Plextronics Inc.) is spin-coated and dried to form a hole injection layer (-40 nm). Thereafter, the organic materials specified below are applied by vapor deposition to the Plexcore ^® coated substrate at a rate of approx. 0.5-5 nm/min at about 10- ⁷ -10- ⁹ mbar. As a hole transport, compound (SH-1 ) is applied by vapor deposition in a thickness of 10 nm doped with MoO _x (-10%) to improve the conductivity.

As exciton and electron blocker, (HTM-1 ; for preparation, see Ir complex

(7) in the application WO2005/019373), is applied to the substrate with a thickness of

10 nm. Subsequently, a mixture of 10% by weight of emitter compound,

(BE-1), 5% by weight of compound (HTM-1) and 85% by weight of compound (SH-1 ) are applied by vapor deposition in a thickness of 40 nm. Subsequently, material (SH-1) is applied by vapour deposition with a thickness of 5 nm as blocker. Thereafter, a 20 nm thick e is deposited consisting of 50% by weight of

(ETM-1), and of 50% of (Liq). Finally a 2 nm

KF layer serves as an electron injection layer and a 100 nm-thick Al electrode completes the device.

All fabricated parts are sealed with a glass lid and a getter in an inert nitrogen atmosph

Application Examples 1 and 2

Comparative Application Example 1 is repeated except that the exciton blocker, (HTM-1), and the host (SH-1 ) are replaced by compounds (A-8) and (A-1), respectively.

OLED characterization

To characterize the OLED, electroluminescence spectra are recorded at various currents and voltages. In addition, the current-voltage characteristic is measured in combination with the light output emitted. The light output is converted to photometric parameters by calibra- tion with a photometer. The results are shown in Table 2. Data are given at luminance (L) = 1000 Cd/m ² except otherwise stated.

Table 2

¹⁾ External quantum efficiency (EQE) is # of generated photons escaped from a substance or a device / # of electrons flowing through it.

It is evident that the CIEy is reduced by replacing EBL/host (HTM-1 )/(SH-1) by (A-8)/(A-8) and (A-1)/(A-1 ), respectively. Reducing the CIEy color coordinate corresponds directly to a deeper blue color. Comparative Application Example 2

The device is fabricated and characterized as described in Comparative Application Example 1 except for the following:

As a hole transport and exciton/electron blocker, (HTM-1), is applied to the substrate with a thickness of 20 nm, wherein the first 10 nm are doped with MoO _x (-10%) to improve the conductivity. Subsequently, a mixture of 10% by weight of emitter compound, (BE-1 ), 5% by weight of compound (HTM-1) and 85% by weight of compound (SH-1) is applied by vapor deposition in a thickness of 40 nm. Subsequently, material (SH-1) is applied by vapour deposition with a thickness of 5 nm as blocker. The ETL is evaporated according to application example 2.

Application Examples 3 and 4

Comparative Application Examples 2 is repeated except that except that the host (SH-1 ) and the hole blocking layer are fully replaced by compound (A-8) and (A-1 ), respectively. The device results are shown in Table 3. Data are given at luminance (L) = 1000 Cd/m ² except otherwise stated.

Table 3

The results shown in Table 3 demonstrate that the CIEy is blue shifted significantly when using compounds (A-8) and (A-1 ) as host instead of reference compound (SH-1). Although the new materials are ultra high bandgap hosts the voltage for these devices is comparable or only slightly larger than for the reference device, which is not an ultrahigh bandgap material.

Application Example 5 - Determination of triplet energy

The triplet energies of the materials are directly determined from the onsets of the measured phosphorescence spectra of the thin films of neat materials. Thin pristine films are prepared by first dissolving 2.5 mg of the material in 0.25 ml di- chloromethane respectively, and second doctor-blading the solutions onto pre-cleaned quartz-slides with a thin film applicator of 30 μιη slot width (Erichsen, Model 360 02082).

The 2% in PMMA films are prepared by dissolving 1 mg of the respective material in 370 μΙ of a dichloromethane solution containing 10 wt% PMMA. A thin film applicator of 60 μιη slot width (Erichsen, Model 360 02082) is used for doctor-blading.

For measurement the resulting thin film samples are inserted into a liquid-helium cryostat Optistat CF (Oxford Instruments) and cooled to a temperature of 4-5K. The phosphores- cence spectra are measured with a fluorescence/phosphorescence spectrometer FLS- 920P (Edinburgh Instruments). The samples are excited with an electrically pulsed LED model UVTOP 315-HL-T039 (Fa. Roithner, Vienna) with a center wavelength of 320 nm and a pulse width of 5 s. The emission spectra are detected via time-gated spectroscopy with a delay-time of 260 \is. The triplet energies (Ti) are determined from the onset of the phosphorescence spectra, the results are shown in the table below.

Compo ention has larger triplet energy than the reference

pound (V-1 ; correspondes to compound B-1 of

WO2014009317).