NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS AND ORGANIC ELECTROLUMINESCENCE DEVICES CONTAINING THEM

Abstract

The present invention relates to compounds of the general formula (11), to a material for an organic electroluminescence device comprising of least one of these compounds, to an organic electroluminescence device comprising at least one of these compounds, and to the use of a compound according to general formula (11) in an organic electroluminescence device as a host material or an electron transporting material.

Description

TECHNICAL FIELD

The present invention relates to compounds of general formulae (I) and (11), to an electronic device comprising at least one of these compounds, to an emitting layer, preferably present in an electronic device, comprising at least one compound of general formula (I) or (11) and to the use of a compound according to general formula (I) or (11) in an electronic device as a host material, a charge transporting material, a charge and/or exciton blocking material, preferably as a host material or an electron transporting material.

Background Art

Quinazolines, carbazoles, and their use in electronic devices are known from the related art.

KR 20150111106 A discloses compounds according to the following formulae:

and their use as electroluminescent device materials.

Carlos M. Martinez et al., J. Heterocyclic Chem., 44, 1035 (2007), disclose Quinalozin-derivatives according to the following formula:

wherein X may be O or H₂ and R₁, R₂, R₃ and R₄ may be hydrogen, R₁ and R₂ may form a six membered ring or R₃ and R₄ may be an additional bond, and a process for their preparation. This document further discloses that the mentioned compounds show activities in a number of pharmaceutical applications based on their sedative, CNS-depressant, neuroleptic, hypnotic, analgesic, diuretic, anthelminthic, antimicrobial, antitubercular, antibiotic antihypertensive, antiinflammatory and antitumoral properties.

US 2015/0255726 A1 discloses compounds according to the following formulae:

etc., wherein X₂ and X₃ may be nitrogen, each of R₁ to R₄, R₇ to R₁₆, R₁₈ to R₂₀, R₂₂ to R₂₅ may be alkyl, aryl, or heteroaryl, and L₁ may be direct bond or arylene. Only the compounds having the following structure:

wherein R₁ to R₄ and R₇ to R₁₆ are all hydrogen, are actually described as exemplified compounds. This document further discloses their use as electroluminescent device materials.

Kimio Hirano, et al., J. Org. Chem. 2011, 76, 9068-9080 discloses compounds according to the following formulae:

wherein R is hydrogen or tosyl. This document teaches nothing about their use.

CITATION LIST

Patent Literature

• KR 20150111106 A
• US 2015/0255726 A1

Non Patent Literature

• Carlos M. Martinez et al., J. Heterocyclic Chem., 44, 1035 (2007)
• Kimio Hirano, et al., J. Org. Chem. 2011, 76, 9068-9080

SUMMARY OF INVENTION

Technical Problem

There remains a need for electronic devices comprising new materials, especially as a host material, a charge transporting material, a charge and/or exciton blocking material to provide improved property, such as efficiency and/or driving voltage of electronic devices.

Accordingly, it is an object of the present invention, with respect to the aforementioned related art, to provide materials suitable for use in electronic devices, preferably OLEDs, and further applications in organic electronics. More particularly, it should be possible to provide electronic devices comprising new compounds as electron transport materials, as hole transport materials or as host materials. The materials should be suitable especially for OLEDs which comprise at least one emitter, which is preferably a phosphorescence emitter, for example at least one red phosphorescent emitter, especially as a host material. The materials should also be suitable especially for OLEDs which comprise at least one emitter, which is preferably a fluorescence emitter, for example at least one blue fluorescent emitter, especially as an electron transporting material.

Furthermore, the materials should be suitable for providing electronic devices, preferably OLEDs, which ensure good efficiencies and a low use and operating voltage of the OLEDs.

Solution to Problem

Said object is solved by the compound of general formula (I):

whereinX¹ is CR¹ or N,X² is CR² or N,X³ is CR³ or N,X⁴ is CR⁴ or N,X⁵ is CR⁵ or N,X⁶ is CR⁶ or N,X⁷ is CR⁷ or N,X⁸ is CR⁸ or N,X⁹ is CR⁹ or N,X¹⁰ is CR¹⁰ or N,wherein X¹ and X³ are not CR¹ and CR³ at the same time,Y is selected from NR¹¹, O or S,R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and R¹¹ are independently of each other selected from H, E, a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, a C₁-C₂₅alkyl group, which is unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E,orat least two of R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ or R¹⁰, if present at adjacent carbon atoms, together form at least one C₆-C₁₈aryl or C₁-C₁₈heteroaryl ring or ring system,o is independently of each other 0 or 1, p is independently of each other 0 or 1, q is independently of each other 0 or 1 and r is independently of each other 0 or 1,

L¹, L², L³ and L⁴ are independently of each other selected from a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E, C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E,

R¹⁴ is independently of each other selected from H, E, a C₆-C₂₄aryl group which is unsubstituted or substituted by at least one group E, C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, a C₁-C₂₅alkyl group which unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E,D is independently of each other —CO—, —COO—, —S—, —SO—, —SO₂—, —O—, —CR¹⁵═CR¹⁶—, —NR¹⁷—, —SiR²²R²³—, —POR²⁵—, —C≡C—,E is independently of each other —OR²¹, —SR²¹, —NR¹⁷R¹⁸, —COR²⁰, —COOR¹⁹, —CONR¹⁷R¹⁸, —CN, —SiR²²R²³R²⁴, halogen, a C₆-C₆₀aryl group which is unsubstituted or is substituted by at least one —F, —CF₃, —CF₂CF₃, —CF₂CF₂CF₃, —CF(CF₃)₂, —(CF₂)₃CF₃ or —C(CF₃)₃, a C₁-C₁₈ alkyl or a C₁-C₁₈alkyl group which is interrupted by at least one O, a C₁-C₆₀heteroaryl group which is unsubstituted or substituted by at least one —F, —CF₃, —CF₂CF₃, —CF₂CF₂CF₃, —CF(CF₃)₂, —(CF₂)₃CF₃ or —C(CF₃)₃,R¹⁵ and R¹⁶ are independently of each other H, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈alkyl group or a C₁-C₁₈alkyl group which is interrupted by at least one O,R¹⁷ and R¹⁸ are independently of each other H, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈alkyl group or a C₁-C₁₈alkyl group, which is interrupted by at least one O, orR¹⁷ and R¹⁸ together form a five or six membered aliphatic, aromatic or heteroaromatic ring,R¹⁹ is H, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈alkyl group or a C₁-C₁₈alkyl group, which is interrupted by at least one O,R²⁰ is H or a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈ alkyl group or a C₁-C₁₈alkyl group, which is interrupted by at least one O,R²¹ is independently of each other H, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈alkyl group or a C₁-C₁₈alkyl group, which is interrupted by at least one O,R²², R²³ and R²⁴ are independently of each other H, a C₁-C₁₈alkyl group, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group, andR²⁵ is H, a C₁-C₁₈alkyl group, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E.

The object of the present invention is also solved by the compound of general formula (11):

• • wherein
  • L¹⁰⁰ is selected from a direct bond, an arylene group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G, or a heteroarylene group having 5 to 30 ring atoms which is unsubstituted or substituted by at least one group G;
  • n¹⁰⁰ is an integer selected from 1 to 4;
  • R¹⁰⁰ is selected from a hydrogen atom, an aryl group having 6 to 30 carbon atoms which is unsubstituted or substituted by at least one group G, a heterocyclic group having 3 to 30 ring atoms which is unsubstituted or substituted by at least one group G, or an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G;
  • R¹⁰¹, R¹⁰², R¹⁰³, R¹⁰⁴, R¹⁰⁵, R¹⁰⁶, R¹⁰⁷, R¹⁰⁸, R¹⁰⁹, R¹¹⁰, R¹¹¹, R¹¹², R¹¹³, R¹¹⁴, R¹¹⁵, and R¹¹⁶ are independently of each other and selected from a hydrogen atom, a halogen atom, a cyano group, an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G, an alkenyl group having 2 to 25 carbon atoms which is unsubstituted or substituted by at least one group G, an alkynyl group having 2 to 25 carbon atoms which is unsubstituted or substituted by at least one group G, a cycloalkyl group having 3 to 25 carbon atoms which is unsubstituted or substituted by at least one group G, an alkoxy group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G, an aryl group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G, a heterocyclic group having 3 to 30 ring atoms which is unsubstituted or substituted by at least one group G, an aryloxy group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G, an alkylthio group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G, an arylthio group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G, a mono-, di-, or tri-substituted silyl group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G and an aryl group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G, a mono- or di-substituted amino group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G and an aryl group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G, a substituted carbonyl group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G and an aryl group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G, and —P(═O)R¹²⁰R¹²¹, wherein R¹²⁰ and R¹²¹ are independently of each other selected from an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G, an aryl group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G, and a heterocyclic group having 3 to 30 ring atoms which is unsubstituted or substituted by at least one group G;
  • G is independently of each other and selected from a halogen atom, a cyano group, an alkyl group having 1 to 25 carbon atoms, an alkenyl group having 2 to 25 carbon atoms, an alkynyl group having 2 to 25 carbon atoms, a cycloalkyl group having 3 to 25 carbon atoms, an alkoxy group having 1 to 25 carbon atoms, an aryl group having 6 to 30 ring carbon atoms, a heterocyclic group having 3 to 30 ring atoms, an aryloxy group having 6 to 30 ring carbon atoms, an alkylthio group having 1 to 25 carbon atoms, an arylthio group having 6 to 30 ring carbon atoms, a mono-, di-, or tri-substituted silyl group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms and an aryl group having 6 to 30 ring carbon atoms, a mono- or di-substituted amino group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms and an aryl group having 6 to 30 ring carbon atoms, a substituted carbonyl group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms and an aryl group having 6 to 30 ring carbon atoms, and —P(═O)R¹²⁰R¹²¹, wherein R¹²⁰ and R¹²¹ are independently of each other and selected from an alkyl group having 1 to 25 carbon atoms, an aryl group having 6 to 30 ring carbon atoms, and a heterocyclic group having 3 to 30 ring atoms;
  • two selected from R¹⁰⁵ to R¹¹⁶ do not form a ring structure; and
  • two selected from R¹⁰¹ to R¹⁰⁴, which are present at adjacent two ring carbon atoms, may together form a ring structure.

DESCRIPTION OF EMBODIMENTS

The compounds according to the present invention, the electronic device according to the present invention and the use of the compounds are explained in detail in the following.

According to the present invention the terms halogen, alkyl, aryl, aryloxy and heteroaryl generally have the following meaning, if said groups are not further specified in specific embodiments mentioned below.

Halogen is fluorine, chlorine, bromine and iodine.

C₁-C₂₅alkyl, preferably C₁-C₁₈alkyl, 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-hexamethylhexyl, n-heptyl, isoheptyl, 1,1,3,3-tetramethylbutyl, 1-methylheptyl, 3-methylheptyl, n-octyl, 1,1,3,3-tetramethylbutyl and 2-ethylhexyl, n-nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, or octadecyl. C₁-C₈alkyl is typically methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.-butyl, isobutyl, tert.-butyl, n-pentyl, 2-pentyl, 3-pentyl, 2,2-dimethyl-propyl, n-hexyl, n-heptyl, n-octyl, 1,1,3,3-tetramethylbutyl and 2-ethylhexyl. C₁-C₄alkyl is typically methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.-butyl, isobutyl, tert.-butyl.

C₁-C₂₅alkoxy groups, preferably C₁-C₁₈alkoxy 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 C₁-C₈alkoxy 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, preferably C₁-C₄alkoxy such as typically methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec.-butoxy, isobutoxy, tert.-butoxy.

C₆-C₆₀aryl, preferably C₆-C₂₄aryl, particularly preferably C₆-C₁₈aryl, which optionally can be substituted, is typically phenyl, 4-methylphenyl, 4-methoxyphenyl, naphthyl, especially 1-naphthyl, or 2-naphthyl, biphenylyl, terphenylyl, pyrenyl, 2- or 9-fluorenyl, phenanthryl, or anthryl, which may be unsubstituted or substituted. Phenyl, 1-naphthyl and 2-naphthyl are examples of a C₆-C₁₀aryl group.

C₆-C₂₄aryloxy, which optionally can be substituted, is typically C₆-C₁₀aryloxy, which optionally can be substituted by one, or more C₁-C₈alkyl and/or C₁-C₈alkoxy groups, such as, for example, phenoxy, 1-naphthoxy, or 2-naphthoxy.

C₁-C₆₀heteroaryl, preferably C₂-C₃₀heteroaryl, particularly preferably C₂-C₁₃heteroaryl, represents a ring with five to seven ring atoms or a condensed ring system, wherein nitrogen, oxygen or sulfur are the possible hetero atoms, and is typically a heterocyclic group with 5 to 40 atoms having at least six conjugated π-electrons such as thienyl, benzothiophenyl, dibenzothiophenyl, thianthrenyl, furyl, furfuryl, 2H-pyranyl, benzofuranyl, isobenzofuranyl, dibenzofuranyl, phenoxythienyl, pyrrolyl, imidazolyl, pyrazolyl, pyridyl, bipyridyl, triazinyl, pyrimidinyl, pyrazinyl, pyridazinyl, indolizinyl, isoindolyl, indolyl, indazolyl, purinyl, quinolizinyl, chinolyl, isochinolyl, phthalazinyl, naphthyridinyl, chinoxalinyl, chinazolinyl, cinnolinyl, pteridinyl, carbazolyl, carbolinyl, benzotriazolyl, benzoxazolyl, phenanthridinyl, acridinyl, pyrimidinyl, phenanthrolinyl, phenazinyl, isothiazolyl, phenothiazinyl, isoxazolyl, furazanyl, 4-imidazo[1,2-a]benzimidazoyl, 5-benzimidazo[1,2-a]benzimidazoyl, benzimidazolo[2,1-b][1,3]benzothiazolyl, carbazolyl, or phenoxazinyl, which can be unsubstituted or substituted. Benzimidazo[1,2-a]benzimidazo-5-yl, benzimidazo[1,2-a]benzimidazo-2-yl, carbazolyl and dibenzofuranyl are examples of a C₂-C₁₄heteroaryl group.

C₇-C₂₅aralkyl is for example benzyl, 2-benzyl-2-propyl, β-phenyl-ethyl, α,α-dimethylbenzyl, ω-phenyl-butyl, ω,ω-dimethyl-ω-phenyl-butyl, ω-phenyl-dodecyl, ω-phenyl-octadecyl, ω-phenyl-eicosyl or ω-phenyl-docosyl, preferably C₇-C₁₈aralkyl such as benzyl, 2-benzyl-2-propyl, β-phenyl-ethyl, α,α-dimethylbenzyl, ω-phenyl-butyl, ω,ω-dimethyl-ω-phenyl-butyl, ω-phenyl-dodecyl or ω-phenyl-octadecyl, and particularly preferred C₇-C₁₂aralkyl such as benzyl, 2-benzyl-2-propyl, β-phenyl-ethyl, α,α-dimethylbenzyl, ω-phenyl-butyl, or ω,ω-dimethyl-ω-phenylbutyl, in which both the aliphatic hydrocarbon group and aromatic hydrocarbon group may be unsubstituted or substituted. Preferred examples are benzyl, 2-phenylethyl, 3-phenylpropyl, naphthylethyl, naphthylmethyl, and cumyl.

C₅-C₁₂cycloalkyl is for example cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, cycloundecyl, cyclododecyl, preferably cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl, which may be unsubstituted or substituted.

Possible preferred substituents of the above-mentioned groups are C₁-C₈alkyl, a hydroxyl group, a mercapto group, C₁-C₈alkoxy, C₁-C₈alkylthio, halogen, halo-C₁-C₈alkyl, or a cyano group.

In an aspect, the present invention relates to a compound of general formula (I):

wherein X¹, X², X³, X⁴, X⁵, X⁸, X⁷, X⁸, X⁹, X¹⁰ and Y have the meanings as mentioned above.

Preferred embodiments are explained in the following.

In general X¹ is CR¹ or N and X³ is CR³ or N, wherein the meanings of R¹ and R³ are explained above. According to the present invention, in general formula (I) X¹ and X³ are not CR¹ and CR³ at the same time, meaning that at least one of X¹ and X³ is N, whereas the other one is CR¹ or CR³, or both of X¹ and X³ are N.

According to a preferred embodiment, the present invention relates to the compound according to the present invention, wherein X¹ and X³ are N. Compounds of this preferred type correspond to the following formula (II):

wherein X², X⁴, X⁵, X⁶, X⁷, X⁸, X⁹, X¹⁰ and Y have the same meanings as mentioned above.

According to a further preferred embodiment the present invention relates to the compound according to the present invention, wherein X¹ is CR¹ and X³ is N or X, is N and X³ is CR³, wherein R¹ and R³ have independently of each other the meanings as mentioned above. Compounds of these preferred types correspond to the following formulae (III) and (IV):

wherein X², X⁴, X⁵, X⁶, X⁸, X⁹, X¹⁰, Y, R¹ and R³ have the same meanings as mentioned above.

According to a particularly preferred embodiment, the present invention relates to the compound according to the present invention, wherein X¹ is N and X³ is CR³, wherein R³ has the meanings as mentioned above.

In general formula (I) and in particular in general formulae (II), (III) and (IV), Y may be selected from NR¹¹, O or S, wherein R¹¹ has the meanings as mentioned above.

Therefore the present invention preferably relates to compounds according to the following general formulae (IIa), (IIb) and (IIc):

wherein independently of each other X², X⁴, X⁵, X⁶, X⁷, X⁸, X⁹, X¹⁰ and R¹¹ have the same meanings as mentioned above.

Further preferred, the present invention relates to compounds according to the following general formulae (IIIa), (IIIb) and (IIIc):

wherein independently of each other X², X⁴, X⁵, X⁶, X⁷, X⁸, X⁹, X¹⁰, R¹ and R¹¹ have the same meanings as mentioned above.

Further preferred, the present invention relates to compounds according to the following general formulae (IVa), (IVb) and (IVc):

wherein independently of each other X², X⁴, X⁵, X⁶, X⁷, X⁸, X⁹, X¹⁰, R³ and R¹¹ have the same meanings as mentioned above.

In general, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and R¹¹, if present, are independently of each other selected from H, E, a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, a C₁-C₂₅alkyl group, which is unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E,

orat least two of R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ or R¹⁰, if present at adjacent carbon atoms, together form at least one C₆-C₁₈aryl or C₁-C₁₈heteroaryl ring or ring system,o is independently of each other 0 or 1, p is independently of each other 0 or 1, q is independently of each other 0 or 1 and r is independently of each other 0 or 1,L¹, L², L³ and L⁴ are independently of each other selected from a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E, C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E,R¹⁴ is independently of each other selected from H, E, a C₆-C₂₄aryl group which is unsubstituted or substituted by at least one group E, C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, a C₁-C₂₅alkyl group which unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E,D is independently of each other —CO—, —COO—, —S—, —SO—, —SO₂—, —O—, —CR¹⁵═CR¹⁶—, —NR¹⁷—, —SiR²²R²³—, —POR²⁵—, —C≡C—, preferably —O—, —NR¹⁷—, —SiR²²R²³—,

E is independently of each other —OR²¹, —SR²¹, —NR¹⁷R¹⁸, —COR²⁰, —COOR¹⁹, —CONR¹⁷R¹⁸, —CN, —SiR²²R²³R²⁴, —POR²⁵R²⁷, halogen, a C₆-C₆₀aryl group which is unsubstituted or is substituted by at least one —F, —CF₃, —CF₂CF₃, —CF₂CF₂CF₃, —CF(CF₃)₂, —(CF₂)₃CF₃ or —C(CF₃)₃, a C₁-C₁₈ alkyl or a C₁-C₁₈alkyl group which is interrupted by at least one O, a C₁-C₆₀heteroaryl group which is unsubstituted or substituted by at least one —F, —CF₃, —CF₂CF₃, —CF₂CF₂CF₃, —CF(CF₃)₂, —(CF₂)₃CF₃ or —C(CF₃)₃, preferably E is independently of each other selected from —NR¹⁷R¹⁸, —CN, —SiR²²R²³R²⁴ or —POR²⁵R²⁶,

R¹⁵ and R¹⁶ are independently of each other H, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈alkyl group or a C₁-C₁₈alkyl group which is interrupted by at least one O, preferably H,R¹⁷ and R¹⁸ are independently of each other H, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈alkyl group or a C₁-C₁₈alkyl group, which is interrupted by at least one O, preferably H, C₁-C₁₈ alkyl group,R¹⁷ and R¹⁸ together form a five or six membered aliphatic, aromatic or heteroaromatic ring, preferably five or six membered aliphatic ring,R¹⁹ is H, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈alkyl group or a C₁-C₁₈alkyl group, which is interrupted by at least one O, preferably H, a C₆-C₁₈aryl group which is unsubstituted or a C₁-C₁₈alkyl group,R²⁰ is H or a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈ alkyl group or a C₁-C₁₈alkyl group, which is interrupted by at least one O, preferably H, a C₆-C₁₈aryl group which is unsubstituted or a C₁-C₁₈alkyl group,R²¹ is independently of each other H, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈alkyl group or a C₁-C₁₈alkyl group, which is interrupted by at least one O, preferably H, a C₆-C₁₈aryl group which is unsubstituted or a C₁-C₁₈alkyl group,R²², R²³ and R²⁴ are independently of each other H, a C₁-C₁₈alkyl group, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group, preferably H, a C₆-C₁₈aryl group which is unsubstituted or a C₁-C₁₈alkyl group, andR²⁵ and R²⁷ are independently of each other H, a C₁-C₁₈alkyl group, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E, preferably H, a C₆-C₁₈aryl group which is unsubstituted or a C₁-C₁₈alkyl group.

According to the present invention, in general, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and R¹¹, if present, are independently of each other selected from a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_rR¹⁴, a C₁-C₂₅alkyl group, which is unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, wherein o is independently of each other 0 or 1, p is independently of each other 0 or 1, q is independently of each other 0 or 1 and r is independently of each other 0 or 1, and L¹, L², L³ and L⁴ are independently of each other selected from a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E, C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, wherein R¹⁴ has the meanings as mentioned above.

Preferably, in formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴ o is independently of each other 1, p is independently of each other 1, q is independently of each other 1 and r is independently of each other 1. This preferred embodiment means that L¹ is present, followed by L², followed by L³, followed by L⁴, followed by R¹⁴.

According to a further preferred embodiment, o is independently of each other 1, p is independently of each other 1, q is independently of each other 1 and r is independently of each other 0. This preferred embodiment means that L¹ is present, followed by L², followed by L³, followed by R¹⁴, wherein L⁴ is not present.

According to a further preferred embodiment, o is independently of each other 1, p is independently of each other 1, q is independently of each other 0 and r is independently of each other 0. This preferred embodiment means that L¹ is present, followed by L², followed by R¹⁴, wherein L³ and L⁴ are not present.

According to a further preferred embodiment, o is independently of each other 1, p is independently of each other 0, q is independently of each other 0 and r is independently of each other 0. This preferred embodiment means that L¹ is present, followed by R¹⁴, wherein L⁴, L³ and L² are not present.

According to a further preferred embodiment, o is independently of each other 0, p is independently of each other 0, q is independently of each other 0 and r is independently of each other 0. This preferred embodiment means that the compounds are substituted by R¹⁴, wherein L⁴, L³, L² and L¹ are not present.

Preferably L¹, L², L³ and L⁴ are independently of each other, if present, selected from a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E or from a C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E. According to a further preferred embodiment, L¹. L², L³ and L⁴ are independently of each other, if present, selected from a C₆-C₄₀aryl group which is unsubstituted or from a C₁-C₂₄heteroaryl group which is unsubstituted.

According to a preferred embodiment, wherein o is independently of each other 1, p is independently of each other 0, q is independently of each other 0 and r is independently of each other 0, L¹ is selected from a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E, preferably unsubstituted, or from a C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, preferably unsubstituted.

According to a further preferred embodiment, wherein o is independently of each other 1, p is independently of each other 1, q is independently of each other 0 and r is independently of each other 0, L¹ is selected from a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E and L² is selected from a C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E.

According to a further preferred embodiment, wherein o is independently of each other 1, p is independently of each other 1, q is independently of each other 1 and r is independently of each other 0, L¹ is selected from a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E, preferably unsubstituted, L² is selected from a C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, preferably unsubstituted, and L³ is selected from a C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, preferably unsubstituted.

In general R¹⁴ can be selected from the group as mentioned above. Preferably, R¹⁴ is hydrogen.

According to a particularly preferred embodiment, the present invention relates to the compounds according to the present invention, wherein R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ and R¹⁰ are independently of each other selected from H, a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, wherein L¹, L², L³ and L⁴ are independently of each other selected from a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E or C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, and R¹⁴ is independently of each other selected from H or a C₁-C₂₅alkyl group which unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, wherein o, p, q, r, E and D have the meanings and preferred meanings as mentioned above.

Further preferred, the present invention relates to compounds according to the present invention, wherein R¹, R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ and R¹⁰, if present, are independently of each other selected from H, a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E or a C₁-C₂₄ N-comprising heteroaryl group which is unsubstituted or substituted by at least one group E,

andR² is selected from a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, wherein L¹, L², L³ and L⁴ are independently of each other selected from a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E or C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, and R¹⁴ is independently of each other selected from H or a C₁-C₂₅alkyl group which unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, wherein L¹, L², L³, L⁴, o, p, q, r, E and D have the meanings and preferred meanings as mentioned above.

Particularly preferred, the present invention relates to compounds according to the present invention, wherein R¹, R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ and R¹⁰, if present, are H

andR² is selected from a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, wherein L¹, L², L³ and L⁴ are independently of each other selected from a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E or C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, and R¹⁴ is independently of each other selected from H or a C₁-C₂₅alkyl group which unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, wherein L¹, L², L³, L⁴, o, p, q, r, E and D have the meanings and preferred meanings as mentioned above.

According to another preferred embodiment of the present invention in the compound according to general formula (I) at least two of R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ or R¹⁰, if present at adjacent carbon atoms, together form at least one C₆-C₁₈aryl or C₁-C₁₈heteroaryl ring or ring system.

According to this embodiment, two of R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ or R¹⁰, if present at adjacent carbon atoms, together form one C₆-C₁₈aryl or C₁-C₁₈heteroaryl ring or ring system. At the same time further two of R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ or R¹⁰, if present at adjacent carbon atoms, may together form at least one further C₆-C₁₈aryl or C₁-C₁₈heteroaryl ring or ring system. According to the present invention two of R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ or R¹⁰ in each case, if present at adjacent carbon atoms, can together form at least one, two, three or four C₆-C₁₈aryl or C₁-C₁₈heteroaryl rings or ring systems.

Preferred C₆-C₁₈aryl or C₁-C₁₈heteroaryl rings or ring systems are for example fused phenylene or naphthylene rings, five or six membered fused C₁-C₁₈heteroarylene rings or ringsystems.

Further preferred, the present invention relates to compounds according to the present invention, wherein R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ and R¹⁰, if present, are independently of each other selected from H or a N-heteroaryl group according to general formula (XII):

whereinn is an integer of 0 to 8,m is an integer of 0 to 4,M is a C₆-C₄₀ arylene group which is unsubstituted or substituted by at least one group E, a C₁-C₂₄heteroarylene group which is unsubstituted or substituted by at least one group E or a C₁-C₂₅ alkylene group which unsubstituted or substituted by at least one group E and/or interrupted by at least one group D,R²⁶ is independently of each other selected from E, a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, a C₁-C₂₅alkyl group, which is unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, wherein o, p, q, r, L¹, L², L³, L⁴, R¹⁴, E and D have the meanings as mentioned above,orat least two of R²⁶, if present at adjacent carbon atoms, may form at least one five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring or ring system, to which at least one further aromatic and/or heteroaromatic ring or ringsystem may be fused.

According to this preferred embodiment of the present invention the N-heteroaryl group according to general formula (XII) is a very specific embodiment of the group of formula -(L¹)_o-(L²)_p(L³)_q-(L⁴)_r-R¹⁴ as defined above.

In particular, the N-heteroaryl group according to general formula (XII) is defined as follows.

In general, n is an integer of 0 to 8, wherein n describes the number of substituents R²⁶ present. If n is 0, no substituent R²⁶ is present, but all eight positions at the fused phenyl rings carry a hydrogen. In case that at least one substituent R²⁶ is present at least one hydrogen at the fused phenyl rings is replaced by this at least one substituent R²⁶.

According to a further embodiment of the present invention at least two of R²⁶, if present at adjacent carbon atoms, may form at least one five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring or ring system, to which at least one further aromatic or heteroaromatic ring or ringsystem may be fused to Preferably, the at least at least one further aromatic ring or ringsystem may comprise 5 to 40 carbon atoms, and the at least at least one further heteroaromatic ring or ringsystem may comprise 1 to 40 carbon atoms and heteroatoms like N, O, P or S.

According to this embodiment, at least two of R²⁶, if present at adjacent carbon atoms, may form at least one five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring or ring system, in combination with further substituents R²⁶ selected from E, a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, a C₁-C₂₅alkyl group, which is unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, wherein o, p, q, r, L¹, L², L³, L⁴, R¹⁴, E and D have the meanings as mentioned above,

orat least two of R²⁶, if present at adjacent carbon atoms, may form at least one five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring or ring system, to which at least one further aromatic and/or heteroaromatic ring or ringsystem may be fused, without further substituents R²⁶.

According to this embodiment at least two substituents R²⁶, if present at adjacent carbon atoms, may form at least one five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring or ring system, i.e. that two substituents that are present at adjacent carbon atoms, may form a five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring or ring system, and that further substituents R²⁶, that are present at further two adjacent carbon atoms, may form a further five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring or ring system. Therefore, one, two, three or four, preferably one or two, five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring(s) or ring system(s) may be present at the N-heteroaryl group according to general formula (XII).

According to a further preferred embodiment of the present invention at least two substituents R²⁶, if present at adjacent carbon atoms, may form a structure according to general formula (XVII):

wherein R⁵³, R⁵⁴, R⁵⁵ and R⁵⁶ are independently of each other selected from H, E, a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, a C₁-C₂₅alkyl group, which is unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, wherein o, p, q, r, L¹, L², L³, L⁴, R¹⁴, E and D have the meanings as mentioned above, preferably H,orat least two of R⁵³, R⁵⁴, R⁵⁵ or R⁵⁶, if present at adjacent carbon atoms, may form at least one five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring or ring system, to which further aromatic and/or heteroaromatic rings or ring systems may be fused.

Particularly preferred, two of R²⁶, if present at adjacent carbon atoms, form a fused phenyl ring, a fused naphthyl ring, a fused phenanthryl ring, a fused carbazole ring, a fused dibenzofuran ring, a fused dibenzothiophene ring, a fused fluorene ring, and a fused fluoranthene ring, wherein, if a fused fluoranthene ring is present it is built up by three of R²⁶.

In formula (XVII), the dashed bindings are bond to the compound of general formula (XII).

Examples of substituents according to general formula (XII), in which at least two of R²⁶ form at least one five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring or ring system, to which at least one further aromatic and/or heteroaromatic ring or ring system may be fused, are shown in the following:

According to a preferred embodiment of the present invention the N-heteroaryl group according to general formula (XII) corresponds to the heteroaryl group according to the following formula (XIII):

wherein M, m and R²⁶ have the meanings as mentioned above, n is 0 to 4,R²⁸, R²⁹, R³⁰, R³¹, R³⁷ and R³⁸ are independently of each other selected from H, E, a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, a C₁-C₂₅alkyl group, which is unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E, preferably H, phenyl, biphenyl,orat least two of R²⁸, R²⁹, R³⁰, R³¹, R³⁷ or R³⁸, if present at adjacent carbon atoms, together form at least one C₆-C₁₈aryl or C₁-C₁₈heteroaryl ring or ring system, andQ and T are independently of each other selected from direct bond, S, O, SiR³²R³³, CR³⁴R³⁵ or NR³⁶,wherein R³² and R³³ are independently of each other H, a C₁-C₁₈alkyl group, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group, preferably H, a C₆-C₁₈aryl group which is unsubstituted or a C₁-C₁₈alkyl group, preferably H, methyl, ethyl, or phenyl,R³⁴ and R³⁵ are independently of each other H, E, a C₆-C₂₄aryl group which is unsubstituted or substituted by at least one group E, C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, a C₁-C₂₅alkyl group which unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E, or spiro group, wherein R³⁴ and R³⁵ together form a five or six membered, substituted or unsubstituted, aliphatic ring, preferably H, methyl, ethyl, phenyl, or spiro group, wherein R³⁴ and R³⁵ together form a five or six membered, substituted or unsubstituted, aliphatic ring,R³⁶ is H, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈alkyl group or a C₁-C₁₈alkyl group, which is interrupted by at least one O, preferably H, a C₆-C₁₈aryl group which is unsubstituted or a C₁-C₁₈alkyl group,wherein D and E have the same meanings as mentioned above.

According to a particularly preferred embodiment of the present invention, in the compound of formula (XIII), Q is direct bond, T is NR³⁶, R³⁶ is phenyl, R³⁷ and R³⁸ are H, m is 0, n is 0 and R²⁸, R²⁹, R³⁰ and R³¹ are H.

According to a further preferred embodiment, the heteroaryl group according to general formula (XIII) corresponds to general formula (XIV):

wherein R²⁶, R²⁸, R²⁹, R³⁰, R³¹, M, Q, T, n and m have the same meanings as mentioned above andR³⁹, R⁴⁰, R⁴¹, R⁴² are independently of each other selected from H, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈alkyl group or a C₁-C₁₈alkyl group, which is interrupted by at least one O, preferably H, a C₆-C₁₈aryl group which is unsubstituted or a C₁-C₁₈alkyl group, preferably R³⁹, R⁴⁰, R⁴¹ and R⁴² are H.

According to a particularly preferred embodiment of the present invention, in the compound of formula (XIV), Q is direct bond, T is S, R³⁹, R⁴⁰, R⁴¹ and R⁴² are H, m is 0 or 1, n is 0 and R²⁸, R²⁹, R³⁰ and R³¹ are H.

According to a further particularly preferred embodiment of the present invention, in the compound of formula (XIV), Q is direct bond, T is NR³⁶, R³⁶ is phenyl, R³⁹, R⁴⁰, R⁴¹ and R⁴² are H, m is 0, n is 0 and R²⁸, R²⁹, R³⁰ and R³¹ are H.

According to a particularly preferred embodiment of the present invention, in the compound of formula (XIV), Q is direct bond, T is CR³⁴R³⁵, R³⁴ and R³⁵ are methyl, R³⁹, R⁴⁰, R⁴¹ and R⁴² are H, m is 0, n is 0 and R²⁸, R²⁹, R³⁰ and R³¹ are H.

According to a further particularly preferred embodiment of the present invention, in the compound of formula (XIV), Q is S, T is direct bond, R³⁹, R⁴⁰, R⁴¹ and R⁴² are H, m is 0, n is 0 and R²⁸, R²⁹, R³⁰ and R³¹ are H.

According to a further particularly preferred embodiment of the present invention, in the compound of formula (XIV), Q is NR³⁶, T is direct bond, R³⁶ is phenyl, R³⁹, R⁴⁰, R⁴¹ and R⁴² are H, m is 0, n is 0 and R²⁸, R²⁹, R³⁰ and R³¹ are H.

According to a further preferred embodiment of the present invention the N-heteroaryl group according to general formula (XII) corresponds to the heteroaryl group according to the following formula (XV):

wherein M, m and R²⁶ have the meanings as mentioned above, n is 0 to 4,R²⁸, R²⁹, R³⁰, R³¹, R⁴³ and R⁴⁴ are independently of each other selected from H, E, a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, a C₁-C₂₅alkyl group, which is unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E, preferably H,orat least two of R²⁸, R²⁹, R³⁰ or R³¹, if present at adjacent carbon atoms, together form at least one C₆-C₁₈aryl or C₁-C₁₈heteroaryl ring or ring system, andQ and T are independently of each other selected from direct bond, S, O, SiR³²R³³, CR³⁴R³⁵ or NR³⁶,wherein R³² and R³³ are independently of each other H, a C₁-C₁₈alkyl group, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group, preferably H, a C₆-C₁₈aryl group which is unsubstituted or a C₁-C₁₈alkyl group, preferably H, methyl, ethyl or phenyl,R³⁴ and R³⁵ are independently of each other H, E, a C₆-C₂₄aryl group which is unsubstituted or substituted by at least one group E, C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, a C₁-C₂₅alkyl group which unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E, or spiro group, wherein R³⁴ and R³⁵ together form a five or six membered, substituted or unsubstituted, aliphatic ring, preferably H, ethyl, ethyl, phenyl, and spiro group, wherein R³⁴ and R³⁵ together form a five or six membered, substituted or unsubstituted, aliphatic ring,R³⁶ is H, a C₆-C₁₈aryl group which is unsubstituted or substituted by at least one C₁-C₁₈alkyl group or at least one C₁-C₁₈alkoxy group, a C₁-C₁₈alkyl group or a C₁-C₁₈alkyl group, which is interrupted by at least one O, preferably H, a C₆-C₁₈aryl group which is unsubstituted or a C₁-C₁₈alkyl group, for example phenyl,wherein D and E have the same meanings as mentioned above.

According to a particular preferred embodiment of the present invention in substituent according to general formula (XV), m is 0, n is 0, R²⁸, R²⁹, R³⁰, R³¹, R⁴³ and R⁴⁴ are H, Q is a direct bond, T is CR³⁴R³⁵, R³⁴ and R³⁵ are methyl.

According to a further particular preferred embodiment of the present invention in substituent according to general formula (XV), m is 0, n is 2, R²⁸, R²⁹, R³⁰, R³¹, R⁴³ and R⁴⁴ are H, two R²⁶ that are present at adjacent carbon atoms together form a fused phenyl ring, which is preferably present in position of R³⁰ and R³¹, Q is a direct bond, T is CR³⁴R³⁵, R³⁴ and R³⁵ are methyl.

According to a further preferred embodiment of the present invention, in substituent according to general formulae (XII), (XIII), (XIV) or (XV) R²⁶ may correspond to the following formula (XVI):

wherein R⁴⁵, R⁴⁶, R⁴⁷, R⁴⁸, R⁴⁹, R⁵⁰, R⁵¹ and R⁵² are independently of each other H, E, a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, a C₁-C₂₅alkyl group, which is unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E,orat least two of R⁴⁶, R⁴⁷, R⁴⁹, R⁵⁰, R⁵¹ or R⁵², if present at adjacent carbon atoms, together form at least one C₆-C₁₈aryl or C₁-C₁₈heteroaryl ring or ring system,wherein E, D, L¹, L², L³, L⁴, o, p, q and r have the same meanings as mentioned above.

Particularly preferred R⁴⁵, R⁴⁶, R⁴⁷, R⁴⁹, R⁵⁰, R⁵¹ and R⁵² are independently of each other H, E, a unsubstituted C₆-C₁₈aryl group or a C₆-C₁₈aryl group substituted with at least one group E, or a C₁-C₂₅alkyl group, which is unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, preferably H, phenyl, biphenyl, naphthyl, phenanthryl or dimethylfluorenyl.

R⁴⁸ is particularly preferred H, a unsubstituted C₆-C₁₈aryl group or a C₆-C₁₈aryl group substituted with at least one group E, preferably phenyl, biphenyl or naphthyl.

Further preferred at least two of R⁴⁶, R⁴⁷, R⁴⁹, R⁵⁰, R⁵¹ or R⁵², most preferably R⁵¹ and R⁵² if present at adjacent carbon atoms, together form at least one C₆-C₁₈aryl or C₁-C₁₈heteroaryl ring or ring system, most preferably a fused phenyl ring.

According to a particularly preferred embodiment, in general formula (XVI) R⁴⁵, R⁴⁶, R⁴⁷, R⁴⁹, R⁵⁰, R⁵¹ and R⁵² are H and R⁴⁸ is phenyl.

According to a further particularly preferred embodiment, in general formula (XVI) R⁴⁵, R⁴⁶, R⁴⁷, R⁴⁹ and R⁵⁰ are H, R⁵¹ and R⁵² form a fused phenyl ring and R⁴⁸ is phenyl.

In general, m is an integer of 0 to 4, wherein m describes the number of groups M present. If m is 0, no group M is present, but the N-heteroaryl group according to general formula (XII) is directly attached to carbon atom within the skeleton of the compound of general formula (I). Preferably, m is 0, 1, 2 or 3, more preferably, m is 0 or 1.

Preferably, M is a C₆-C₄₀ arylene group which is unsubstituted, a C₁-C₂₄heteroarylene group which is unsubstituted or a C₁-C₂₅ alkylene group which unsubstituted. Particularly preferred, M is a C₆-C₁₈ arylene group which is unsubstituted, most preferably a phenylene group.

Preferably, R²⁶ is independently of each other selected from a group of formula -(L¹)_o-(L²)_p-(L³)_q(L⁴)_r-R¹⁴, wherein o, p, q, r, L¹, L², L³, L⁴ and R¹⁴ have the meanings and preferred meanings as mentioned above.

According to a very preferred embodiment of the present invention, m is 0, and at least two of R²⁶, if present at adjacent carbon atoms, form at least one five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring or ring system, without further substituents R²⁶.

According to a further very preferred embodiment of the present invention, m is 1, M is M is a C₆-C₄₀arylene group which is unsubstituted or substituted by at least one group E, preferably phenylene, and at least two of R²⁶, if present at adjacent carbon atoms, form a five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring or ring system, without further substituents R²⁶.

The present invention therefore preferably relates the compound according to the present invention, wherein m is 1, M is a C₆-C₄₀arylene group which is unsubstituted or substituted by at least one group E, preferably phenylene, and at least two of R²⁶, if present at adjacent carbon atoms, form a five or six membered, substituted or unsubstituted, saturated, unsaturated, aromatic or heteroaromatic ring, wherein E has the meanings as mentioned above.

The present invention further preferably relates to the compound according to the present invention, wherein R² is a N-heteroaryl group according to general formula (XII) as defined above.

The present invention further preferably relates to the compound according to the present invention, wherein R¹, R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ and R¹⁰ are H and R² is a N-heteroaryl group according to general formula (XII) as defined above.

R¹¹, if present, are independently of each other selected from H, E, a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, a C₁-C₂₅alkyl group, which is unsubstituted or substituted by at least one group E and/or interrupted by at least one group D, a C₇-C₂₅aralkyl which is unsubstituted or substituted by at least one group E, a C₅-C₁₂cycloalkyl group which is unsubstituted or substituted by at least one group E. Preferably, R¹¹ is a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, wherein general and preferred embodiments of this group are mentioned above. Particularly preferred, R¹¹ is a group of formula -(L¹)_o-(L²)_p-(L³)_q-(L⁴)_r-R¹⁴, wherein o is 1, p, q and r are 0 and L¹ is independently of each other selected from a C₆-C₄₀aryl group which is unsubstituted or substituted by at least one group E or C₁-C₂₄heteroaryl group which is unsubstituted or substituted by at least one group E, and R¹⁴ is H. Most preferably, R¹¹ is phenyl.

According to the present invention, in compounds according to general formula (I), in particular in compounds according to general formulae (II), (III) or (IV), more preferred in compounds according to general formula (IIa), (IIb), (IIc), (IIIa), (IIIb), (IIIc), (IVa), (IVb) or (IVc), X⁴, X⁵, X⁶, X⁷, X⁸, X⁹ and X¹⁰ can independently of each other be N, CR⁴, CR⁵, CR⁶, CR⁷, CR⁸, CR⁹ or CR¹⁰, wherein R⁴ to R¹⁰ have the same meanings as mentioned above. But, according to a preferred embodiment of the present invention non of X⁴, X⁵, X⁶, X⁷, X⁸, X⁹ and X¹⁰ is N. i.e. beside X¹ and/or X³, optionally Y, and optionally N present in any substituent at X¹, X³ or Y, no further N atoms are present in the molecule.

The present invention preferably relates to compounds according to the present invention, wherein X² is CR², X⁴ is CR⁴, X⁵ is CR⁵, X⁶ is CR⁶, X⁷ is CR⁷, X⁸ is CR⁸, X⁹ is CR⁹ and X¹⁰ is CR¹⁰, wherein R², R⁴, R⁵, R⁶, R⁷, R⁸, R⁹ and R¹⁰ have the meanings as mentioned above.

The present invention therefore preferably relates to compounds according to the following formulae (IId), (IIe) and (IIf):

wherein independently of each other R², R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and R¹¹ have the same meanings as mentioned above. Most preferably, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and R¹¹ are H and R² has the meanings as mentioned above.

Further preferred, the present invention preferably relates to compounds according to the following general formulae (IIId), (IIIe) and (IIIf):

wherein independently of each other R¹, R², R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and R¹¹ have the same meanings as mentioned above. Most preferably, R¹, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and R¹¹ are H and R² has the meanings as mentioned above.

Further preferred, the present invention preferably relates to compounds according to the following general formulae (IVd), (IVe) and (IVf):

wherein independently of each other R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and R¹¹ have the same meanings as mentioned above. Most preferably, R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁹ and R¹¹ are H and R² has the meanings as mentioned above.

In another aspect, the present invention relates to a compound of general formula (11):

R¹⁰¹, R¹⁰², R¹⁰³, R¹⁰⁴, R¹⁰⁵, R¹⁰⁶, R¹⁰⁷, R¹⁰⁸, R¹⁰⁹, R¹¹⁰, R¹¹¹, R¹¹², R¹¹³, R¹¹⁴, R¹¹⁵, and R¹¹⁶ are independently of each other and selected froma hydrogen atom,a halogen atom,a cyano group,an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G,an alkenyl group having 2 to 25 carbon atoms which is unsubstituted or substituted by at least one group G,an alkynyl group having 2 to 25 carbon atoms which is unsubstituted or substituted by at least one group G,a cycloalkyl group having 3 to 25 carbon atoms which is unsubstituted or substituted by at least one group G,an alkoxy group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G,an aryl group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G,a heterocyclic group having 3 to 30 ring atoms which is unsubstituted or substituted by at least one group G,an aryloxy group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G,an alkylthio group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G,an arylthio group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G,a mono-, di-, or tri-substituted silyl group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G and an aryl group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G,a mono- or di-substituted amino group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G and an aryl group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G,a substituted carbonyl group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G and an aryl group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G, anda group represented by —P(═O)R¹²⁰R¹²¹, wherein R¹²⁰ and R¹²¹ are independently of each other selected from an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G, an aryl group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G, and a heterocyclic group having 3 to 30 ring atoms which is unsubstituted or substituted by at least one group G.

According to the present invention, halogen, alkyl group, alkenyl group, alkynyl group, cycloalkyl group, alkoxy group, aryl group, heterocyclic group, aryloxy group, alkylthio group, arylthio group, mono-, di-, or tri-substituted silyl group, mono- or di-substituted amino group, substituted carbonyl group, and —P(═O)R¹²⁰R¹²¹ generally have the following meanings, if said groups are not further specified in specific embodiments mentioned below.

Halogen is fluorine, chlorine, bromine and iodine, preferably fluorine.

Alkyl group having 1 to 25, preferably 1 to 18, more preferably 1 to 8 carbon atoms is linear or branched. Examples are a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a s-butyl group, a t-butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, an undecyl group, a dodecyl group, a tridecyl group, a tetradecyl group, an octadecyl group, and a tetracosanyl group. Preferred exas are a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a s-butyl group, a t-butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, an undecyl group, a dodecyl group, a tridecyl group, a tetradecyl group, and an octadecyl group, and more preferred examples are a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a s-butyl group, a t-butyl group, a pentyl group, a hexyl group, a heptyl group, and an octyl group.

Alkenyl group having 2 to 25, preferably 2 to 18, more preferably 2 to 8 carbon atoms is linear or branched. Examples are a vinyl group, a 2-propenyl group, an isopropenyl group, an allyl group, a butenyl group, a hexenyl group, and a decenyl group, preferably a vinyl group, a 2-propenyl group, an isopropenyl group and an allyl group, and more preferably a vinyl group and a 2-propenyl group.

Alkynyl group having 2 to 25, preferably 2 to 18, more preferably 2 to 8 carbon atoms is linear or branched. Examples are an ethynyl group, a propargyl group, and a 3-pentynyl group.

Cycloalkyl group having 3 to 25, preferably 3 to 10, more preferably 3 to 8 carbon atoms is, for example, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, and an adamantyl group, with a cyclopentyl group and a cyclohexyl group being preferred.

Alkoxy group having 1 to 25, preferably 1 to 18, more preferably 1 to 8 carbon atoms is linear or branched. Examples are a methoxy, an ethoxy group, a n-propoxy group, an isopropoxy group, an n-butoxy group, a s-butoxy group, a tert-butoxy group, an amyloxy group, an isoamyloxy group, a t-amyloxy group, a heptyloxy group, an octyloxy group, an isooctyloxy group, a nonyloxy group, a decyloxy group, an undecyloxy group, a dodecyloxy group, a tetradecyloxy group, a pentadecyloxy group, a hexadecyloxy group, a heptadecyloxy group and an octadecyloxy group. Preferred examples are a methoxy, an ethoxy group, a n-propoxy group, an isopropoxy group, an n-butoxy group, a s-butoxy group, and a tert-butoxy group.

Aryl group having 6 to 30, preferably 6 to 25, more preferably 6 to 18 ring carbon atoms is a single ring group, a ring assembly group, or a fused ring group (fused aryl group) having 10 to 30, preferably 10 to 25, more preferably 10 to 18 ring carbon atoms. Examples are a phenyl group, a naphthyl group, a biphenylyl group, a terphenylyl group, a quarterphenylyl group, an acenaphthylenyl group, an anthryl group, a benzanthryl group, an aceanthryl group, a phenanthryl group, a benzophenanthryl group, a phenalenyl group, a fluorenyl group, a 9,9′-spirobifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a benzonaphthofluorenyl group, a picenyl group, a pentaphenyl group, a pentacenyl group, a pyrenyl group, a chrysenyl group, a benzochrysenyl group, a s-indacenyl group, an as-indacenyl group, a fluoranthenyl group, a benzofluoranthenyl group, a tetracenyl group, a triphenylenyl group, a benzotriphenylenyl group, a perylenyl group, a coronyl group, a dibenzanthryl group, a 9,9-dimethylfluorenyl group, and a 9,9-diphenylfluorenyl group. Preferred example are a phenyl group, a naphthyl group, a biphenylyl group, a phenanthryl group, a fluoranthenyl group, a triphenylenyl group, a benzotriphenylenyl group, a 9,9-dimethylfluorenyl group, and a 9,9-diphenylfluorenyl group.

Heterocyclic group having 3 to 30, preferably 3 to 24, more preferably 3 to 20 ring atoms includes at least one, preferably 1 to 5, more preferably 1 to 3, and still more preferably 1 or 2 hetero atoms which may be the same or different, for example, a nitrogen atom, a sulfur atom, and an oxygen atom. The heterocyclic group may be a non-aromatic heterocyclic group having 3 to 30, preferably 3 to 24, more preferably 3 to 20 ring atoms or an aromatic heterocyclic group (heteroaryl group) having 5 to 30, preferably 5 to 24, more preferably 5 to 20 ring atoms, each being a single ring group, a ring assembly group, or a fused ring group.

Examples of the non-aromatic heterocyclic group are an aziridinyl, an oxiranyl group, a thiiranyl group, an imidazolidinyl group, an imidazolinyl group, an indolinyl group, an oxazolidinyl group, an oxazolinyl group, an oxetanyl group, an azetidinyl group, a thietanyl group, a dioxanyl group, a dioxolanyl group, a thiazolinyl group, a piperazinyl group, a piperidinyl group, a tetrahydropyranyl group, a tetrahydrothiopyranyl group, a pyrazolidinyl group, a pyrazolinyl group, a pyrrolidinyl group, a tetrahydrofuranyl group, a tetrahydothienyl group, and a pyrrolinyl group.

Examples of the heteroaryl group are a pyrrolyl group, a furyl group, a thienyl group, a pyridyl group, a pyridazinyl group, a pyrimidinyl group, a pyrazinyl group, a triazinyl group, an imidazolyl group, an oxazolyl group, a thiazolyl group, a pyrazolyl group, an isoxazolyl group, an isothiazolyl group, an oxadiazolyl group, a thiadiazolyl group, a triazolyl group, a tetrazolyl group, an indolyl group, an isoindolyl group, an isobenzothiophenyl group, an indolizinyl group, a quinolizinyl group, a quinolyl group, an isoquinolyl group, a cinnolyl group, a phthalazinyl group, a quinazolinyl group, a quinoxalinyl group, a benzimidazolyl group, a benzoxazolyl group, a benzothiazolyl group, an indazolyl group, a benzisoxazolyl group, a benzisothiazolyl group, a benzofuranyl group, a dibenzofuranyl group, an azadibenzofuranyl group, a benzothiophenyl group, a dibenzothiophenyl group, an azadibenzothiophenyl group, a carbazolyl group, a biscarbazolyl group, an azacarbazolyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a phenothiazinyl group, a phenoxazinyl group, an azatriphenylenyl group, a diazatriphenylenyl group, a xanthenyl group, a (benzo)naphtofuranyl group, a (benzo)naphthothiopenyl group, a benzocarbazolyl group, an indolocarbazolyl group, a (benzofurano)carbazolyl group, a (benzothieno)carbazolyl group, a (benzothieno)pyrimidinyl group, a (benzofurano)pyrimidinyl group, an indenopyrimidinyl group, a benzo(benzofurano)pyridyl group, and a benzo(benzothieno)pyridyl group.

Aryloxy group having 6 to 30, preferably 6 to 25, more preferably 6 to 18 ring carbon atoms includes the aryl portion which is selected from the aryl group mentioned above or its preferred examples, and preferably a phenoxy group, 1-naphthoxy group, or a 2-naphthoxy group.

Alkylthio group having 1 to 25, preferably 1 to 18, more preferably 1 to 8 carbon atoms include the alkyl portion which is selected from the alkyl group mentioned above, its preferred examples, or its more preferred examples, and preferably a methylthio group, an ethylthio group, a n-propylthio group, an isopropylthio group, a n-butylthio group, an isobutylthio group, a s-butylthio group, a t-butylthio group, a pentylthio group, a hexylthio group, a heptylthio group, and an octylthio group.

Arylthio group having 6 to 30, preferably 6 to 25, more preferably 6 to 18 ring carbon atoms includes the aryl portion which is selected from the aryl group mentioned above or its preferred examples, and preferably a phenylthio group, 1-naphthylthio group, or a 2-naphthylthio group.

Mono-, di-, or tri-substituted silyl group has one to three substituents which are independently selected from the alkyl group mentioned and the aryl group mentioned above, for example, a monoalkylsilyl group, a dialkylsilyl group, a trialkylsilyl group, a monoarylsilyl group, a diarylsilyl group, a triarylsilyl group, an alkyldiarylsilyl group, and a dialkylarylsilyl group, with a monoalkylsilyl group, a dialkylsilyl group, a trialkylsilyl group, a monoarylsilyl group, a diarylsilyl group, and a triarylsilyl group being preferred and a trialkylsilyl group and a triarylsilyl group being more preferred. Examples are a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a propyldimethylsilyl group, an isopropyldimethylsilyl group, a triphenylsilyl group, a phenyldimethylsilyl group, a t-butyldiphenylsilyl group, and a tritolylsilyl group. Preferred are a trimethylsilyl group, a triethylsilyl group, a triphenylsilyl group, and a phenyldimethylsilyl group, with a trimethylsilyl group and a triphenylsilyl group being more preferred.

Mono- or di-substituted amino group has one or two substituents which are independently selected from the alkyl group mentioned above and the aryl group mentioned above, for example, a monoalkyl amino group, a monoarylamino group, a dialkylamino group, a diarylamino group, and a alkylarylamino group, preferably a methylamino group, an ethylamino group, a phenylamino group, a dimethylamino group, a diethylamino group, a methylethylamino group, a diphenylamino group, a dinaphthylamino group, and a phenylnaphthyl group.

Substituted carbonyl group has a substituent which is selected from the alkyl group mentioned above and the aryl group mentioned above, preferably a methylcarbonyl group, an ethylcarbonyl group, and a phenylcarbonyl group.

R¹²⁰ and R¹²¹ of a group represented by —P(═O)R¹²⁰R¹²¹ are independently of each other and selected from the alkyl group mentioned above, the aryl group mentioned above, and the heterocyclic group mentioned above, preferably —P(═O)(methyl)₂, —P(═O)(ethyl)₂, —P(═O)(phenyl)₂.

Two selected from R¹⁰¹, R¹⁰², R¹⁰³, and R¹⁰⁴, which are present at adjacent two ring carbon atoms, may together form a ring structure, preferably a five or six membered, aromatic or non-aromatic hydrocarbon ring or a five or six membered, aromatic or non-aromatic heterocyclic ring, which is unsubstituted or substituted by at least one group G, and to which a five or six membered, aromatic or non-aromatic hydrocarbon ring and/or a five or six membered, aromatic or non-aromatic heterocyclic ring may be fused.

According to an embodiment of the invention, two selected from R¹⁰¹, R¹⁰², R¹⁰³, and R¹⁰⁴, which are present at adjacent two ring carbon atoms, do not form a ring structure.

Any of two selected from R¹⁰⁵, R¹⁰⁶, R¹⁰⁷, R¹⁰⁸, R¹⁰⁹, R¹¹⁰, R¹¹¹, R¹¹², R¹¹³, R¹¹⁴, R¹¹⁵, and R¹¹⁶ do not form a ring structure.

According to an embodiment of the invention, R¹⁰¹, R¹⁰², R¹⁰³, R¹⁰⁴, R¹⁰⁵, R¹⁰⁶, R¹⁰⁷, R¹⁰⁸, R¹⁰⁹, R¹¹⁰, R¹¹¹, R¹¹², R¹¹³, R¹¹⁴, R¹¹⁵, and R¹¹⁶, preferably one of R¹⁰², R¹⁰³, and R¹¹¹ is selected from the aryl group mentioned above and the heterocyclic group mentioned above, and preferably selected from a phenyl group, a fluoranthenyl group, and the heteroaryl group according to any of general formulae (24) to (33) mentioned below.

According to an embodiment of the invention, R¹⁰¹, R¹⁰², R¹⁰³, R¹⁰⁴, R¹⁰⁵, R¹⁰⁶, R¹⁰⁷, R¹⁰⁸, R¹⁰⁹, R¹¹⁰, R¹¹¹, R¹¹², R¹¹³, R¹¹⁴, R¹¹⁵, and R¹¹⁶ are preferably all hydrogen atoms.

G is independently of each other and selected from a halogen atom, a cyano group, an alkyl group having 1 to 25 carbon atoms, an alkenyl group having 2 to 25 carbon atoms, an alkynyl group having 2 to 25 carbon atoms, a cycloalkyl group having 3 to 25 carbon atoms, an alkoxy group having 1 to 25 carbon atoms, an aryl group having 6 to 30 ring carbon atoms, a heterocyclic group having 3 to 30 ring atoms, an aryloxy group having 6 to 30 ring carbon atoms, an alkylthio group having 1 to 25 carbon atoms, an arylthio group having 6 to 30 ring carbon atoms, a mono-, di-, or tri-substituted silyl group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms and an aryl group having 6 to 30 ring carbon atoms, a mono- or di-substituted amino group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms and an aryl group having 6 to 30 ring carbon atoms, a substituted carbonyl group, wherein the substituent is selected from an alkyl group having 1 to 25 carbon atoms and an aryl group having 6 to 30 ring carbon atoms, and a group represented by —P(═O)R¹²⁰R¹²¹, wherein R¹²⁰ and R¹²¹ are independently of each other selected from an alkyl group having 1 to 25 carbon atoms, an aryl group having 6 to 30 ring carbon atoms, and a heterocyclic group having 3 to 30 ring atoms. The above groups have the meanings mentioned above with respect to R¹⁰¹ to R¹¹⁶. Each group G may be unsubstituted or substituted by at least one of the groups mentioned above.

L¹⁰⁰ of formula (11) is selected from a direct bond, an arylene group having 6 to 30, preferably 6 to 25, more preferably 6 to 18 ring carbon atoms which is unsubstituted or substituted by at least one group G, or a heteroarylene group having 5 to 30, preferably 5 to 25, more preferably 5 to 18 ring atoms which is unsubstituted or substituted by at least one group G.

The arylene group is a group formed when one hydrogen atom is removed from the aryl group mentioned above with respect to R¹⁰¹ to R¹¹⁶, for example, a phenylene group, a naphthylene group, and a biphenylene group, preferably a p-phenylene group, a m-phenylene group, a naphthalene-2,7-diyl group, a naphthalene-1,4-diylgroup, and a biphenyl-4,4′-diyl group.

The heteroarylene group is a group formed when one hydrogen atom is removed from the heteroaryl group mentioned above with respect to R¹⁰¹ to R¹¹⁶, for example, an imidazolediyl group, a pyridinediyl group, a pyridazinediyl group, a pyradinediyl group, a pyrimidinediyl group, a trizainediyl group, a pyrrolediyl group, a frandiyl group, a thiophenediyl group, and a quinazolinediyl group.

According to a preferred embodiment, L¹⁰⁰ is selected from a direct bond and the arylene group mentioned above.

n¹⁰⁰ is an integer of 1 to 4, preferably 1 to 3, more preferably 1 or 2, and still more preferably 1.

According to a preferred embodiment, n¹⁰⁰ is 1 and L¹⁰⁰ is the arylene group mentioned above.

According to another preferred embodiment, n¹⁰⁰ is 1 and L¹⁰⁰ is a direct bond.

R¹⁰⁰ is selected from a hydrogen atom, an aryl group having 6 to 30 carbon atoms which is unsubstituted or substituted by at least one group G, a heterocyclic group having 3 to 30 ring atoms which is unsubstituted or substituted by at least one group G, or an alkyl group having 1 to 25 carbon atoms which is unsubstituted or substituted by at least one group G, wherein said groups and G have the meanings mentioned above with respect to R¹⁰¹ to R¹¹⁶.

According to a preferred embodiment, R¹⁰⁰ is selected from the aryl group mentioned above and the heteroaryl group mentioned above.

According to another preferred embodiment, the aryl group for R¹⁰⁰ is selected from a phenyl group, a biphenylyl group, a terphenylyl group, or a fused aryl group having 10 to 30, preferably 10 to 25, more preferably 10 to 18 ring carbon atoms which is unsubstituted or substituted by at least one group G. Examples of the fused aryl group are a naphthyl group, an acenaphthylenyl group, an anthryl group, a benzanthryl group, an aceanthryl group, a phenanthryl group, a benzophenanthryl group, a phenalenyl group, a fluorenyl group, a 9,9′-spirobifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a benzonaphthofluorenyl group, a picenyl group, a pentaphenyl group, a pentacenyl group, a pyrenyl group, a chrysenyl group, a benzochrysenyl group, a s-indacenyl group, an as-indacenyl group, a fluoranthenyl group, a benzofluoranthenyl group, a tetracenyl group, a triphenylenyl group, a perylenyl group, a coronyl group, a dibenzanthryl group, a 9,9-dimethylfluorenyl group, and a 9,9-diphenylfluorenyl group. Preferred are a naphthyl group, a phenanthryl group, a fluoranthenyl group, a triphenylenyl group, a benzochrysenyl group, and a fluorenyl group. More preferred are a naphthyl group, a fluoranthenyl group, a triphenylenyl group, a phenanthryl group, and a fluorenyl group.

According to a preferred embodiment, the aryl group for R¹⁰⁰ is selected from a phenyl, a biphenylyl group, and a fused aryl group having 10 to 30, for example, a naphthyl group, a phenanthrenyl group, a fluoranthenyl group, a triphenylenyl group, and a benzotriphenylenyl group.

According to a preferred embodiment, the heteroaryl group for R¹⁰⁰ is selected from the heteroaryl group mentioned above.

According to another preferred embodiment, the heteroaryl group for R¹⁰⁰ is selected from a heteroaryl group comprising a nitrogen-comprising six membered ring, a dibenzofuranyl group, a dibenzothiophenyl group, and a carbazolyl group, to each of which at least one selected from a six membered, aromatic hydrocarbon ring, a five or six membered, non-aromatic hydrocarbon ring, a five or six membered, aromatic heterocyclic ring, and a five or six membered, non-aromatic heterocyclic ring may be fused to form, for example, a (benzo)naphtofuranyl group, a (benzo)naphthothiopenyl group, a benzocarbazolyl group, an indolocarbazolyl group, a (benzofurano)carbazolyl group, and a (benzothieno)carbazolyl group. These groups may be unsubstituted or substituted by at least one group G.

The heteroaryl group comprising a nitrogen-comprising six membered ring is selected from a pyridyl group, a pyridazinyl group, a pyrimidinyl group, a pyrazinyl group, a triazinyl group, an indolizinyl group, a quinolizinyl group, a quinolyl group, an isoquinolyl group, a cinnolyl group, a phthalazinyl group, a quinazolinyl group, a quinoxalinyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a phenothiazinyl group, a phenoxazinyl group, an azatriphenylenyl group, and a diazatriphenylenyl group, each of which is unsubstituted or substituted by at least one group G. If the heteroaryl group is a fused heteroaryl group, a free bond may present on any of the fused rings, for example, a quinazolinyl group may be a 2-, 4-, 5-, 6-, 7- or 8-quinazolinyl group which is unsubstituted or substituted by at least one group G.

According to a preferred embodiment, the heteroaryl group comprising a nitrogen-comprising six membered ring is of general formula (12):

whereinX⁶¹ is CR⁶¹ or a nitrogen atom,X⁶³ is CR⁶³ or a nitrogen atom,X⁶⁵ is CR⁶⁵ or a nitrogen atom,wherein at least one of X⁶¹, X⁶³, and X⁶⁵ is a nitrogen atom;one of R⁶¹, R⁶², R⁶³, R⁶⁴, R⁶⁵, and R⁶⁶ is a direct bond to L¹⁰⁰, and the others are independently of each other and selected from a hydrogen atom and G, preferably selected from a hydrogen atom and the aryl group mentioned above, more preferably selected from a hydrogen atom, a phenyl group, a biphenylyl group, a naphthyl group, and a phenanthryl group;wherein(a) two of R⁶¹, R⁶², R⁶³, R⁶⁴, R⁶⁵, and R⁶⁶, which are present at adjacent two ring carbon atoms, may together form a ring structure of formula (13) or (14), and further two of R⁶¹, R⁶², R⁶³, R⁶⁴, R⁶⁵, and R⁶⁶, which are present at adjacent two ring carbon atoms, may together form a ring structure of formula (13) or (14):

wherein*a bonds to one of the adjacent two ring carbon atoms, and *b bonds to the other of the adjacent two ring carbon atoms;X⁶⁶ is selected from an oxygen atom, a sulfur atom, NR⁶⁹, or CR⁷⁰R⁷¹;R⁶⁹ is selected from an aryl group having 6 to 30 carbon atoms, a heteroaryl group having 5 to 30 ring atom, and an alkyl group having 1 to 25 carbon atoms, each of which has the meaning mentioned above, preferably selected from the aryl group mentioned above, and more preferably a phenyl group;R⁷⁰ and R⁷¹ are independently of each other and selected from an aryl group having 6 to 30 carbon atoms, a heteroaryl group having 5 to 30 ring atom, and an alkyl group having 1 to 25 carbon atoms, each of which has the meaning mentioned above, preferably selected from the aryl group mentioned above and the alkyl group mentioned above, and more preferably a phenyl group and a methyl group; andR⁶⁷ and R⁶⁸ are independently of each other and selected from a hydrogen atom and G, preferably a hydrogen atom;orR⁶⁷ and R⁶⁸ may together form a five or six membered, aromatic or non-aromatic hydrocarbon ring which is unsubstituted or substituted by at least one group G or a five or six membered, aromatic or non-aromatic heterocyclic ring which is unsubstituted or substituted by at least one group G, to each of which a five or six membered, aromatic or non-aromatic hydrocarbon ring and/or a five or six membered, aromatic or non-aromatic heterocyclic ring may be fused;

wherein*c bonds to one of the adjacent two ring carbon atoms, and *d bonds to the other of the adjacent two ring carbon atoms;R⁷², R⁷³, R⁷⁴, and R⁷⁵ are independently of each other and selected from a hydrogen atom and G; andtwo of R⁷², R⁷³, R⁷⁴, and R⁷⁵, which are present at adjacent two ring carbon atoms, may together form a five or six membered, aromatic or non-aromatic hydrocarbon ring which is unsubstituted or substituted by at least one group G or a five or six membered, aromatic or non-aromatic heterocyclic ring which is unsubstituted or substituted by at least one group G, to each of which a five or six membered, aromatic or non-aromatic hydrocarbon ring and/or a five or six membered, aromatic or non-aromatic heterocyclic ring may be fused;or(b) three of R⁶¹, R⁶², R⁶³, R⁶⁴, R⁶⁵, and R⁶⁶, which are present at consecutive three ring carbon atoms, may together form a fused ring structure which comprises three fused rings each selected from a six membered, aromatic hydrocarbon ring which is unsubstituted or substituted by at least one group G, a five or six membered, non-aromatic hydrocarbon ring which is unsubstituted or substituted by at least one group G, a five or six membered, aromatic heterocyclic ring which is unsubstituted or substituted by at least one group G, and a five or six membered, non-aromatic heterocyclic ring which is unsubstituted or substituted by at least one group G.

According to a preferred embodiment, the heteroaryl group comprising a nitrogen-comprising six membered ring is of general formula (12) is a pyridinyl group, a pyrimidinyl group or a triazinyl group, each of which is unsubstituted or substituted by at least one group G.

The heteroaryl group comprising a nitrogen-comprising six membered ring of general formula (12), wherein two of R⁶¹, R⁶², R⁶³, R⁶⁴, R⁶⁵, and R⁶⁶ together forms a ring structure of formula (14), corresponds to general formula (15):

wherein X⁶¹, X⁶³, R⁶², R⁶⁶, R⁷², R⁷³, R⁷⁴, and R⁷⁵ have the meanings mentioned above.

R⁶², R⁶³, and R⁶⁶ are preferably selected from a hydrogen atom and the aryl group mentioned above, more preferably selected from a hydrogen atom, a phenyl group, a biphenylyl group, a naphthyl group, a phenanthryl group; and R⁷², R⁷³, R⁷⁴, and R⁷⁵ are preferably all hydrogen atoms.

According to a preferred embodiment, formula (15) corresponds to formula (15a) or (15b), preferably (15a):

wherein R⁶², R⁶⁶, R⁷², R⁷³, R⁷⁴, and R⁷⁵ have the meanings mentioned above.

R⁶² and R⁶⁶ are preferably selected from a hydrogen atom and the aryl group mentioned above, more preferably selected from a hydrogen atom, a phenyl group, a biphenylyl group, a naphthyl group, a phenanthryl group; and R⁷², R⁷³, R⁷⁴, and R⁷⁵ are preferably all hydrogen atoms.

According to a preferred embodiment, formula (15) also corresponds to general formulae (15c), (15d), (15e), (15f), (15g) and (15h):

wherein X⁶¹, X⁶³, R⁶², R⁶⁶, R⁷², R⁷³, R⁷⁴, and R⁷⁵ have the meanings mentioned above, and R⁷²a, R⁷²b, R⁷²c, and R^72d are independent of each other and selected from a hydrogen atom and G, preferably a hydrogen atom.

The heteroaryl group comprising a nitrogen-comprising six membered ring of general formula (12), wherein two of R⁶¹, R⁶², R⁶³, R⁶⁴, R⁶⁵, and R⁶⁶ together forms a ring structure of formula (13), wherein R⁶⁷ and R⁶⁸ together forms a five or six membered, aromatic or non-aromatic hydrocarbon ring, corresponds to general formula (16) or (17):

wherein X⁶¹, X⁶³, X⁶⁶, R⁶², and R⁶⁶ have the meanings mentioned above, and R⁷⁶, R⁷⁷, R⁷⁸, and R⁷⁹ are independent of each other and selected from a hydrogen atom and G, preferably a hydrogen atom.

According to a preferred embodiment, formulae (16) and (17) correspond to general formulae (16a) and (16b):

wherein X⁶¹, X⁶³, X⁶⁶, and R⁶⁶ have the meanings mentioned above, and R⁷⁶, R⁷⁷, R⁷⁸, and R⁷⁹ are independent of each other and selected from a hydrogen atom and G, preferably a hydrogen atom. R⁶⁶ is preferably selected from the aryl group mentioned above, more preferably a phenyl group.

According to a more preferred embodiment, formulae (16a) and (17b) correspond to general formulae (16b), (16c), (16d), (17b), (17c), and (17d):

wherein R⁶⁶ has the meaning mentioned above, preferably selected from the aryl group mentioned above, more preferably a phenyl group; and R⁷⁰, R⁷¹, R⁷⁶, R⁷⁷, R⁷⁸, and R⁷⁹ are independent of each other and selected from a hydrogen atom and G, preferably a hydrogen atom.

The heteroaryl group comprising a nitrogen-comprising six membered ring of general formula (12), wherein two of R⁶¹, R⁶², R⁶³, R⁶⁴, R⁶⁵, and R⁶⁶ together forms a ring structure of formula (13) or (14), and further two of R⁶¹, R⁶², R⁶³, R⁶⁴, R⁶⁵, and R⁶⁶ together forms another ring structure of formula (13) or (14), corresponds to any of general formulae (18) to (23):

wherein X⁶⁶, R⁷², R⁷³, R⁷⁴, and R⁷⁵ have the meanings mentioned above, and R⁷⁶, R⁷⁷, R⁷⁸, and R⁷⁹ are independent of each other and selected from a hydrogen atom and G.

According to a preferred embodiment, X⁶⁶ of formulae (18) to (23) is an oxygen atom, a sulfur atom, or a C(CH₃)₂, and R⁷², R⁷³, R⁷⁴, R⁷⁵, R⁷⁶, R⁷⁷, and R⁷⁸ of formulae (18) to (23) are all hydrogen atoms.

Three of R⁶¹, R⁶², R⁶³, R⁶⁴, R⁶⁵, and R⁶⁶ of the heteroaryl group comprising a nitrogen-comprising six membered ring of general formula (12) may together form a fused ring structure which comprises three fused rings each selected from a six membered, aromatic hydrocarbon ring which is unsubstituted or substituted by at least one group G, a five or six membered, non-aromatic hydrocarbon ring which is unsubstituted or substituted by at least one group G, a five or six membered, aromatic heterocyclic ring which is unsubstituted or substituted by at least one group G, and a five or six membered, non-aromatic heterocyclic ring which is unsubstituted or substituted by at least one group G.

The heteroaryl group comprising a nitrogen-comprising six membered ring of general formula (12), wherein three of R⁶¹, R⁶², R⁶³, R⁶⁴, R⁶⁵, and R⁶⁶ together form a fused ring structure which comprises three fused rings, corresponds to formula (24):

wherein X⁶¹ and X⁶⁵ have the meanings mentioned above, and F1, F2, and F3 are independent of each other and selected from a six membered, aromatic hydrocarbon ring which is unsubstituted or substituted by at least one group G, a five or six membered, non-aromatic hydrocarbon ring which is unsubstituted or substituted by at least one group G, a five or six membered, aromatic heterocyclic ring which is unsubstituted or substituted by at least one group G, and a five or six membered, non-aromatic heterocyclic ring which is unsubstituted or substituted by at least one group G.

According to one embodiment, the six membered, aromatic hydrocarbon ring is a benzene ring; the five or six membered, non-aromatic hydrocarbon ring is a cyclopentane ring or a cyclohexane ring; the five or six membered, aromatic heterocyclic ring is selected from the corresponding rings of the heteroaryl group mentioned above; and the five or six membered, non-aromatic hydrocarbon ring is selected from the corresponding rings of the non-aromatic heterocyclic group mentioned above.

According to a preferred embodiment, formula (24) corresponds to formula (25):

whereinX⁶¹ and X⁶⁵ have the meanings mentioned above,Y is selected from an oxygen atom, a sulfur atom, NR⁸⁷, and CR⁸⁸R⁸⁹;R⁸⁷ is selected from an aryl group having 6 to 30 carbon atoms, a heteroaryl group having 5 to 30 ring atom, and an alkyl group having 1 to 25 carbon atoms, each of which has the meaning mentioned above, preferably selected from the aryl group mentioned above, and more preferably a phenyl group;R⁸⁸ and R⁸⁹ are independently of each other and selected from an aryl group having 6 to 30 carbon atoms, a heteroaryl group having 5 to 30 ring atom, or an alkyl group having 1 to 25 carbon atoms, each of which has the meaning mentioned above, preferably selected from the aryl group mentioned above and the alkyl group mentioned above, and more preferably selected from a phenyl group and a methyl group;X⁸⁰ is CR⁸⁰ or a nitrogen atom,X⁸¹ is CR⁸¹ or a nitrogen atom,X⁸² is CR⁸² or a nitrogen atom,X⁸³ is CR⁸³ or a nitrogen atom,X⁸⁴ is CR⁸⁴ or a nitrogen atom,X⁸⁵ is CR⁸⁵ or a nitrogen atom,X⁸⁶ is CR⁸⁶ or a nitrogen atom, andR⁸⁰, R⁸¹, R⁸², R⁸³, R⁸⁴, R⁸⁵, and R⁸⁶ are independently of each other and selected from a hydrogen atom and G,preferablyX⁸⁰ is CR⁸⁰, X⁸¹ is CR⁸¹, X⁸² is CR⁸², X⁸³ is CR⁸³, X⁸⁴ is CR⁸⁴, X⁸⁵ is CR⁸⁵, X⁸⁶ is CR⁸⁶, and R⁸⁰, R⁸¹, R⁸², R⁸³, R⁸⁴, R⁸⁵, and R⁸⁶ are each hydrogen atom.

According to a more preferred embodiment, formulae (24) and (25) correspond to any of formulae (26) to (29):

wherein X⁶¹, X⁶⁵, R⁸⁷, R⁸⁸, and R⁸⁹ have the meanings mentioned above.

According to a still more preferred embodiment, formulae (24) to (29) correspond to any of formulae (30) to (33):

wherein R⁸⁷, R⁸⁸, and R⁸⁹ have the meanings mentioned above.

Preferred compounds according to general formula (11) according to the present invention are shown in the following.

The compound of formula (11) can be synthesized according to the methods described in the synthesis examples below or modified methods thereof.

Compounds According to the Present Invention in Organic Electronics Applications

In the following the use of the compounds according to the present invention in organic electronic applications will be explained. This use will be explained in respect of the compound according to general formulae (I) and (11) according to the present invention. A person having ordinary skill in the art understands that these explanations also and in particular relate to the preferred compounds according to general formulae (ii), (III) or (IV), more preferred in compounds according to general formula (IIa), (IIb), (IIc), (IIIa), (IIIb), (IIIc), (IVa), (IVb) or (IVc), in particular (IId), (IIe), (IIf), (IIId), (IIIe), (IIIf), (IVd), (IVe) or (IVf), the preferred compounds of general formula (11), their preferred embodiments and to the specifically defined molecules that are mentioned in this application.

It has been found that the compounds according to general formulae (I) and (11) 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 present invention therefore also relates to an electronic device comprising at least one compound according to the present invention.

The organic transistor generally includes a semiconductor layer formed from an organic layer with charge 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 layers with charge transport capacity may comprise the compounds according to general formulae (I) and (11) according to the present invention.

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 charge 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 layers with charge transport capacity may comprise a compound according to general formulae (I) and (11) according to the present invention.

The compounds according to general formulae (I) and (11) being particularly suitable in OLEDs for use as a host (=matrix) material, preferably in a light-emitting layer, and/or a charge transport material, for example as a hole transport material and/or as an electron transporting material, charge and/or exciton blocking material, particularly preferably as a host material or as an electron transporting material.

The present invention therefore preferably relates to the electronic device according to the present invention, preferably an organic electroluminescence device, more preferably an organic light emitting diode (OLED), comprising a cathode, an anode, and a plurality of organic layers provided between the cathode and the anode, the organic layers comprising an emitting layer comprising the at least one compound of general formulae (I) and (11), preferably as a host material, a charge transporting material, charge and/or exciton blocking material, particularly preferably as a host material or as an electron transporting material.

The compounds according to general formulae (I) and (11) are preferably suitable in OLEDs as host material, preferably in combination with a red phosphorescence emitter. Further preferred, the compounds according to general formulae (I) and (11) are particularly suitable in OLEDs as an electron transporting material, preferably in a light-emitting layer, especially in combination with preferably a blue fluorescence emitter, and preferably in an electron transport layer.

The present invention therefore preferably relates to the use of a compound according to general formulae (I) and (11) as defined above in an electronic device, preferably in an electroluminescence device, particularly preferably in an organic light emitting diode (OLED), preferably in an emitting layer, as a host material, a charge transporting material, for example as a hole transport material or an electron transport material, preferably as an electron transporting material, as a charge and/or exciton blocking material, preferably as a host material or an electron transporting material.

In the case of use of the inventive compounds according to general formulae (I) and (11) 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. The inventive compounds according to general formulae (I) and (11) are suitable especially for use as matrix and/or charge transport and/or charge blocking materials for green, red and yellow, preferably green and red, more preferably red emitters. The inventive compounds according to general formulae (I) and (11) are further suitable especially for use as electron transporting material for blue emitters. Furthermore, the compounds according to general formulae (I) and (11) can be used as conductor/complementary materials in organic electronics applications selected from switching elements and organic solar cells. According to the present application, the terms matrix and host are used interchangeable.

In the emission layer or one of the emission layers of an OLED, it is also possible to combine an emitter material with at least one matrix material of the compound according to general formulae (I) and (11) and one or more, preferably one, further matrix materials (co-host). This may achieve a high quantum efficiency, low driving voltage and/or long lifetime of these devices.

According to one preferred embodiment of the present invention the compounds according to general formulae (I) and (11) are used as host materials, preferably in emitting layers comprising red light-emitting compounds. According to this embodiment, preferably no further host material is present in the light-emitting layer.

According to another preferred embodiment of the present invention the compounds according to general formulae (I) and (11) are used as host materials, preferably in emitting layers comprising green light-emitting compounds. According to this embodiment, the compounds according to the present invention are preferably used in the presence of at least one further host material, i.e. as a co-host. Further host materials are mentioned in the following.

It is likewise possible that the compounds according to general formulae (I) and (11) are present in two or three of the following layers: in the light-emitting layer (preferably as host material) and/or in the transport layer (as electron transport material).

When a compound according to general formulae (I) and (11) is used as matrix (host) material in an emission layer and additionally as electron transport material, owing to the chemical identity or similarity of the materials, an improved interface between the emission layer and the adjacent material, which can lead to a decrease in the voltage with equal luminance and to an extension of the lifetime of the OLED. Moreover, the use of the same material as electron transport material and/or as matrix of an emission layer allows the production process of an OLED to be simplified, since the same source can be used for the vapor deposition process of the material of one of the compounds of the formula the compound according to general formulae (I) and (11).

Suitable structures of organic electronic devices, especially organic light-emitting diodes (OLED), are known to those skilled in the art and are specified below.

For example, the electronic device, preferably an organic electroluminescence device, more preferably an organic light emitting diode (OLED), according to the present invention comprises a cathode, an anode, and a plurality of organic layers provided between the cathode and the anode, the organic layers comprising an emitting layer comprising the at least one compound of general formula (I) or (11), preferably as a host material, a charge transporting material, for example as a hole transport material or an electron transport material, preferably as an electron transporting material, and/or exciton blocking material, particularly preferably as a host material or as an electron transporting material.

The present invention therefore preferably relates to the electronic device, preferably an organic electroluminescence device, more preferably an organic light emitting diode (OLED), according to the present invention, comprising a cathode, an anode, and a plurality of organic layers provided between the cathode and the anode, the organic layers comprising an emitting layer comprising the at least one compound of general formula (I) or (11), preferably as a host material, a charge transporting material, for example as a hole transport material or an electron transport material, preferably as an electron transporting material, and/or exciton blocking material, particularly preferably as a host material or as an electron transporting material.

More preferably, the present invention provides an organic light-emitting diode (OLED) comprising an anode and a cathode and a light-emitting layer arranged between the anode and the cathode, and if appropriate at least one further layer selected from the group consisting of at least one blocking layer for holes/excitons, at least one blocking layer for electrons/excitons, at least one hole injection layer, at least one hole transport layer, at least one electron injection layer and at least one electron transport layer, wherein the at least one compound according to general formula (I) or (11) is present in the light-emitting layer and/or in at least one of the further layers. The at least one compound according to general formula (I) or (11) is preferably present in the light-emitting layer and/or hole/exciton blocking layer and/or the charge blocking layer, i.e. the electron or hole transport layer.

In a preferred embodiment of the present invention, at least one compound according to general formulae (I) and (11) is used as electron transport material. Examples of preferred compounds according to general formulae (I) and (11) are shown above.

In another preferred embodiment of the present invention, at least one compound of general formulae (I) and (11) is used as charge/exciton blocker material. Examples of preferred compounds according to general formulae (I) and (11) are shown above.

The present application further relates to a light-emitting layer, preferably present in an electronic device, more preferably in an electroluminescence device, particularly preferably in an organic light emitting diode (OLED), comprising at least one compound of general formula (I) or (11) as defined above, preferably as host material or co-host material. Examples of preferred compounds according to general formulae (I) and (11) are shown above.

Most preferably, the electronic device according to the present invention is an organic light emitting diode (OLED).

Structure of the Inventive OLED

The inventive organic light-emitting diode (OLED) thus 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 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 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 embodiments.

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 (Jun. 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 or MTDATA. 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.

An example for a suitable hole injection material is:

(see also hole-transporting molecules)

Hole Transport Layer (c):

According to a preferred embodiment the OLED according to the present invention comprises at least one compound according to general formulae (I) and (11) or their preferred embodiments as a charge transporting material, preferably as a hole transporting layer. In addition to the compounds according to general formulae (I) and (11) or without these compounds 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, US2011/0163302 (triarylamines with (di)benzothiophen/(di)benzofuran; Nan-Xing Hu et al. Synth. Met. 111 (2000) 421 (indolocarbazoles), 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 made, for example, to WO2013/022419, wherein

(HTL1-1) and

(HTL2-1) constitute the hole transport layer.

Customarily used hole-transporting molecules are selected from the group consisting of

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

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

(4-phenyl-N-[4-(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-tolyl)-9,9′-spirobi[fluorene]-2,2′,7,7′-tetramine), 4,4′-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (α-NPD), N,N′-diphenyl-N,N′-bis(3-methylphenyl)-[1,1′-biphenyl]-4,4′-diamine (TPD), 1,1-bis[(di-4-tolylamino)phenyl]cyclohexane (TAPC), N,N′-bis(4-methylphenyl)-N,N′-bis(4-ethylphenyl)[1,1′-(3,3′-dimethyl)biphenyl]-4,4′-diamine (ETPD), tetrakis(3-methylphenyl)-N,N,N′,N′-2,5-phenylenediamine (PDA), α-phenyl-4-N,N-diphenylaminostyrene (TPS), p-(diethylamino)benzaldehyde diphenylhydrazone (DEH), triphenylamine (TPA), bis[4-(N,N-diethylamino)-2-methylphenyl](4-methylphenyl)methane (MPMP), 1-phenyl-3-[p-(diethylamino)styryl]-5[p-(diethylamino)phenyl]pyrazoline (PPR or DEASP), 1,2-trans-bis(9H-carbazol-9-yl)-cyclobutane (DCZB), N,N,N′,N′-tetrakis(4-methylphenyl)-(1,1′-biphenyl)-4,4′-diamine (TTB), fluorine compounds such as 2,2′,7,7′-tetra(N,N-di-tolyl)amino-9,9-spirobifluorene (spiro-TTB), N,N′-bis(naphthalen-1-yl)-N,N′-bis(phenyl)9,9-spirobifluorene (spiro-NPB) and 9,9-bis(4-(N,N-bis-biphenyl-4-yl-amino)phenyl-9H-fluorene, benzidine compounds such as N,N′-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 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 hexacyanohexaazatriphenylene (HAT).

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 MoO₂, MoO₃, WOE, ReO₃ and/or V₂O₅, preferably MoO₃ and/or ReO₃, more preferably MoO₃, 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, 11,11,12,12-tetracyanonaphtho-2,6-quinodimethane, 2-fluoro-7,7,8,8-tetracyanoquino-dimethane, 2,5-difluoro-7,7,8,8-tetracyanoquinodimethane, dicyanomethylene-1,3,4,5,7,8-hexafluoro-6H-naphthalen-2-ylidene)malononitrile (F₆-TNAP), 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.

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 complexes 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 PCT/EP2014/055520. 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.

According to a preferred embodiment of the present invention, at least one compound of general formulae (I) and (11) is present in the exciton blocking layer of the OLED according to the present invention.

Emitting Layer (e)

The light emitting layer is an organic layer having a light emitting function and is formed from one or more layers, wherein one of the layers comprises a host material (first host material), optionally a second host material, and the light emitting material as described below.

When the light emitting layer is composed of two or more layers, the light emitting layer or layers other than that mentioned above contains or contain a host material and a dopant material when a doping system is employed. The major function of the host material is to promote the recombination of electrons and holes and confine excitons in the light emitting layer. The dopant material causes the excitons generated by recombination to emit light efficiently.

In case of a phosphorescent device, the major function of the host material is to confine the excitons generated on the dopant in the light emitting layer.

The light emitting layer may be made into a double dopant layer, in which two or more kinds of dopant materials having high quantum yield are used in combination and each dopant material emits light with its own color. For example, to obtain a yellow emission, a light emitting layer formed by co-depositing a host, a red-emitting dopant and a green-emitting dopant is used.

In a laminate of two or more light emitting layers, electrons and holes are accumulated in the interface between the light emitting layers, and therefore, the recombination region is localized in the interface between the light emitting layers, to improve the quantum efficiency.

The light emitting layer may be different in the hole injection ability and the electron injection ability, and also in the hole transporting ability and the electron transporting ability each being expressed by mobility.

The light emitting layer is formed, for example, by a known method, such as a vapor deposition method, a spin coating method, and LB method. Alternatively, the light emitting layer may be formed by making a solution of a binder, such as resin, and the material for the light emitting layer in a solvent into a thin film by a method such as spin coating.

The light emitting layer is preferably a molecular deposit film. The molecular deposit film is a thin film formed by depositing a vaporized material or a film formed by solidifying a material in the state of solution or liquid. The molecular deposit film can be distinguished from a thin film formed by LB method (molecular build-up film) by the differences in the assembly structures and higher order structures and the functional difference due to the structural differences.

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 emission wavelength of the phosphorescent dopant used in the light emitting layer is not particularly limited. In a preferred embodiment, at least one of the phosphorescent dopants used in the light emitting layer has the peak of emission wavelength of in general 430 nm or longer and 780 nm or shorter, preferably 490 nm or longer and 700 nm or shorter and more preferably 490 nm or longer and 650 nm or shorter. Most preferred are green emitter materials (490 to 570 nm). In another preferred embodiment, red emitter materials (570 to 680 nm) are preferred.

The phosphorescent dopant (phosphorescent emitter material) is a compound which emits light by releasing the energy of excited triplet state and preferably a organometallic complex comprising at least one metal selected from Ir, Pt, Pd, Os, Au, Cu, Re, Rh and Ru and a ligand, although not particularly limited thereto as long as emitting light by releasing the energy of excited triplet state. A ligand having an ortho metal bond is preferred. In view of obtaining a high phosphorescent quantum yield and further improving the external quantum efficiency of electroluminescence device, a metal complex comprising a metal selected from Ir, Os, and Pt is preferred, with iridium complex, osmium complex, and platinum, particularly an ortho metallated complex thereof being more preferred, iridium complex and platinum complex being still more preferred, and an ortho metallated iridium complex being particularly preferred.

According to a particularly preferred embodiment of the present invention, the compounds according to general formulae (I) and (11) can be used as the matrix (=host material) in the light-emitting layer.

Suitable metal complexes for use in the inventive OLEDs, preferably as emitter material, 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 1 211 257 A2, US 2002/0094453 A1, WO 02/02714 A2, WO 00/70655 A2, WO 01/41512 A1, WO 02/15645 A1, WO 2005/019373 A2, WO 2005/113704 A2, WO 2006/115301 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, US2011/0233528, WO2012/048266 and WO2012/172482.

Further suitable metal complexes are the commercially available metal complexes tris(2-phenylpyridine)iridium(III), iridium(III) tris(2-(4-tolyl)pyridinato-N,C^2′), bis(2-phenylpyridine)(acetylacetonato)iridium(III), iridium(III) tris(1-phenylisoquinoline), iridium(III) bis(2,2′-benzothienyl)pyridinato-N,C^3′)(acetylacetonate), tris(2-phenylquinoline)iridium(III), iridium(III) bis(2-(4,6-difluorophenyl)pyridinato-N,C²)picolinate, iridium(III) bis(1-phenylisoquinoline)(acetylacetonate), bis(2-phenylquinoline)(acetylacetonato)iridium(III), iridium(III) bis(di-benzo[th]quinoxaline)(acetylacetonate), iridium(III) bis(2-methyldibenzo[th]quinoxaline)(acetylacetonate) and tris(3-methyl-1-phenyl-4-trimethylacetyl-5-pyrazolino)terbium(III), bis[1-(9,9-dimethyl-9H-fluoren-2-yl)isoquinoline](acetylacetonato)iridium(III), bis(2-phenylbenzothiazolato)(acetylacetonato)iridium(III), bis(2-(9,9-dihexylfluorenyl)-1-pyridine)(acetylacetonato)iridium(III), bis(2-benzo[b]thiophen-2-ylpyridine)(acetylacetonato)iridium(III).

In addition, the following commercially available materials are suitable: tris(dibenzoylacetonato)mono(phenanthroline)europium(III), tris(dibenzoylmethane)mono(phenanthroline)europium(III), tris(dibenzoylmethane)mono(5-aminophenanthroline)europium(III), tris(di-2-naphthoylmethane)mono(phenanthroline)europium(III), tris(4-bromobenzoylmethane)mono(phenanthroline)europium(III), tris(di(biphenyl)methane)mono(phenanthroline)europium(III), tris(dibenzoylmethane)mono(4,7-diphenylphenanthroline)europium(III), tris(dibenzoylmethane)mono(4,7-di-methylphenanthroline)europium(III), tris(dibenzoylmethane)mono(4,7-dimethylphenanthrolinedisulfonic acid)europium(III) disodium salt, tris[di(4-(2-(2-ethoxyethoxy)ethoxy)benzoylmethane)]mono(phenanthroline)europium(III) and tris[di[4-(2-(2-ethoxyethoxy)ethoxy)benzoylmethane)]mono(5-aminophenanthroline)europium(III), osmium(II) bis(3-(trifluoromethyl)-5-(4-tert-butylpyridyl)-1,2,4-triazolato)diphenylmethylphosphine, osmium(II) bis(3-(trifluoromethyl)-5-(2-pyridyl)-1,2,4-triazole)dimethylphenylphosphine, osmium(II) bis(3-(trifluoromethyl)-5-(4-tert-butylpyridyl)-1,2,4-triazolato)dimethylphenylphosphine, osmium(II) bis(3-(trifluoromethyl)-5-(2-pyridyl)pyrazolato)dimethylphenylphosphine, tris[4,4′-di-tert-butyl(2,2′)-bipyridine]ruthenium(III), osmium(II) bis(2-(9,9-dibutylfluorenyl)-1-isoquinoline(acetylacetonate).

Particularly suitable metal complexes are described in US2014048784, US2012223295, US2014367667, US2013234119, US2014001446, US2014231794, US2014008633, WO2012108388 and WO2012108389. The emitters mentioned in US2013234119, paragraph [0222], are exemplified. Selected emitters, especially red emitters, of said emitters mentioned in US2013234119, paragraph [0222], are:

Further suitable Emitters are mentioned in: Mrs Bulletin, 2007, 32, 694:

Further suitable Emitters are mentioned in: WO2009100991:

Further suitable Emitters are mentioned in: WO2008101842:

Further suitable Emitters are mentioned in: US 20140048784, especially in paragraph [0159]:

Further suitable red emitters are shown in WO 2008/109824. Preferred red emitters according to this document are the following compounds:

Further suitable emitters are shown below.

Still further suitable emitter are shown below.

Still further suitable emitter are shown below.

The emitter materials (dopants), preferably the phosphorescent emitter materials, may be used alone or in combination of two or more.

According to a further embodiment of the OLED according to the present invention, the light emitting layer may comprise at least one fluorescent, preferably blue, emitter. Examples of preferred blue dopants that may be present in the light emitting layer of the OLED according to the present invention are polycyclic amine derivatives as mentioned in EP 2924029. Particularly preferred aromatic amine derivatives are selected from compounds according to the following formula (20):

In the formula (20), Y is a substituted or unsubstituted fused aromatic hydrocarbon group including 10 to 50 ring carbon atoms.

Ar₁₀₁, and Ar₁₀₂ are independently a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms or a substituted or unsubstituted heterocyclic ring group including 5 to 50 ring atoms.

Specific examples of Y include the above-mentioned fused aryl group. Y is preferably a substituted or unsubstituted anthryl group, a substituted or unsubstituted pyrenyl group or a substituted or unsubstituted chrysenyl group.

n is an integer of 1 to 4. It is preferred that n be an integer of 1 to 2.

The above-mentioned formula (20) is preferably one represented by the following formulas (21) to (24).

In the formulas (21) to (24), R_e, R_f and R_g are independently a substituted or unsubstituted alkyl group including 1 to 20 carbon atoms, a substituted or unsubstituted alkenyl group including 2 to 50 carbon atoms, a substituted or unsubstituted alkynyl group including 2 to 50 carbon atoms, a substituted or unsubstituted aralykyl group including 1 to 20 carbon atoms, a substituted or unsubstituted cycloalkyl group including 3 to 20 ring carbon atoms, a substituted or unsubstituted alkoxy group including 1 to 20 carbon atoms, a substituted or unsubstituted aryloxy group including 6 to 20 ring carbon atoms, a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms, a substituted or unsubstituted silyl group, a substituted or unsubstituted alkyl germanium group including 1 to 50 carbon atoms or a substituted or unsubstituted aryl germanium group including 6 to 50 ring carbon atoms. R_e, R_f and R_g may independently be bonded to any of the bonding positions of the benzene rings that constitutes the fused polycyclic skeleton.

As preferable examples of R_e, R_f and R_g, a substituted or unsubstituted aryl group including 6 to 50 ring carbon atoms can be given. More preferably, R_e, R_f and R_g are a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, or the like.

t is an integer of 0 to 10. u is an integer of 0 to 8. m is an integer of 0 to 10. Ar₂₀₁ to Ar₂₁₈ are independently an aryl group including 6 to 50 ring carbon atoms or a substituted or unsubstituted heterocyclic group including 5 to 50 ring atoms.

Preferred examples of Ar₂₀₁ to Ar₂₁₈ include a substituted or unsubstituted phenyl group, a substituted or unsubstituted dibenzofuranyl group or the like. As preferable examples of the substituent of Ar₂₀₁ to Ar₂₁₈, an alkyl group, a cyano group and a substituted or unsubstituted silyl group can be given.

In the formulas (21) to (24), as examples of the alkyl group, the alkoxy group, the aryl group, the aryloxy group and the heterocyclic group, those exemplified above can be given.

As the alkenyl group including 2 to 50, preferably 2 to 30, more preferably 2 to 20, and particularly preferably 2 to 10, carbon atoms, a vinyl group, an allyl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group, a 1,3-butanedienyl group, a 1-methylvinyl group, a styryl group, a 2,2-diphenylvinyl group, a 1,2-diphenylvinyl group, a 1-methylallyl group, a 1,1-dimethylallyl group, a 2-methylallyl group, a 1-phenylallyl group, a 2-phenylallyl group, a 3-phenylallyl group, a 3,3-diphenylallyl group, a 1,2-dimethylallyl group, a 1-phenyl-1-butenyl group, a 3-phenyl-1-butenyl group or the like can be given. Preferred are a styryl group, a 2,2-diphenylvinyl group, a 1,2-diphenylvinyl group or the like.

As the alkynyl group including 2 to 50 (preferably 2 to 30, more preferably 2 to 20, particularly preferably 2 to 10) carbon atoms, a propargyl group, a 3-pentynyl group or the like can be given.

As the alkyl germanium group, a methylhydrogermyl group, a trimethylgermyl group, a triethylgermyl group, a tripropylgermyl group, a dimethyl-t-butylgermyl group or the like can be given.

As the aryl germanium group, a phenyldihydrogermyl group, a diphenylhydrogermyl group, a triphenylgermyl group, a tritolylgermyl group, a trinaphthylgermyl group or the like can be given.

As the styrylamine compound and the styryldiamine compound, those represented by the following formulas (17) and (18) are preferable.

In the formula (17), Ar₃₀₁ is a k-valent group; a k-valent group corresponding to a phenyl group, a naphthyl group, a biphenyl group, a terphenyl group, a stilbene group, a styrylaryl group and a distyrylaryl group. Ar₃₀₂ and Ar₃₀₃ are independently an aryl group including 6 to 20 ring carbon atoms, and Ar₃₀₁, Ar₃₀₂ and Ar₃₀₃ may be substituted.

k is an integer of 1 to 4, with an integer of 1 and 2 being preferable. Any one of Ar₃₀₁ to Ar₃₀₃ is a group including a styryl group. It is further preferred that at least one of Ar₃₀₂ and Ar₃₀₃ be substituted by a styryl group.

As for the aryl group including 6 to 20 ring carbon atoms, the above-mentioned aryl group can be specifically given. Preferable examples include a phenyl group, a naphthyl group, an anthranyl group, a phenanthryl group, a terphenyl group or the like.

In the formula (18), Ar₃₀₄ to Ar₃₀₆ are a v-valent substituted or unsubstituted aryl group including 6 to 40 ring carbon atoms. v is an integer of 1 to 4, with an integer of 1 and 2 being preferable.

Here, as the aryl group including 6 to 40 ring carbon atoms in the formula (18), the abovementioned aryl group can be specifically given. A naphthyl group, an anthranyl group, a chrysenyl group, a pyrenyl group or an aryl group represented by the formula (20) is preferable.

As preferable substituents that substitute on the aryl group, an alkyl group including 1 to 6 carbon atoms, an alkoxy group including 1 to 6 carbon atoms, an aryl group including 6 to 40 ring carbon atoms, an amino group substituted by an aryl group including 6 to 40 ring carbon atoms, an ester group including an aryl group that includes 5 to 40 ring carbon atoms, an ester group including an alkyl group that includes 1 to 6 carbon atoms, a cyano group, a nitro group, a halogen atom or the like can be given.

The content of the emitter materials (dopants), preferably the phosphorescent emitter materials, in the light emitting layer is not particularly limited and selected according to the use of the device, and preferably 0.1 to 70% by mass, and more preferably 1 to 30% by mass. If being 0.1% by mass or more, the amount of light emission is sufficient. If being 70% by mass or less, the concentration quenching can be avoided. The further component in the emitting layer is usually one or more host material, which is preferably present in an amount of 30 to 99.9% by mass, more preferably 70 to 99% by mass, wherein the sum of the emitter material(s) and the host material(s) is 100% by mass.

Further possible fluorescent blue emitters that may be present in the emitting layer of the OLED according to the present invention are mentioned in US2012112169.

Host (Matrix) Materials

The light-emitting layer may comprise further components in addition to the emitter material. For example, a fluorescent 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 the case that one or more phosphorescent emitter materials are used in the light emitting layer, one or more phosphorescent hosts are employed as host material. The phosphorescent host is a compound which confines the triplet energy of the phosphorescent dopant efficiently in the light emitting layer to cause the phosphorescent dopant to emit light efficiently.

In a preferred embodiment, the light-emitting layer is formed of at least one emitter material and of at least one of the matrix materials mentioned in this application. According to a preferred embodiment, the electronic device according to the present invention, preferably the OLED according to the present invention, comprises at least one compound according to general formula (I) or (11) as matrix (host) material.

According to one embodiment, the light-emitting layer comprises at least one emitter material and at least two matrix materials, wherein one of the matrix materials is a compound according to general formula (I) or (11) and the other matrix material(s) is/are used as co-host(s). Suitable other host materials than the compounds of general formulae (I) and (11) (co-hosts) are mentioned below. This embodiment is preferably realized with emitter materials that emit red light.

According to another embodiment, the light-emitting layer comprises at least one emitter material and a compound according to general formula (I) or (11) as a single matrix material. Examples of preferred compounds of general formulae (I) and (11) useful as single host material are shown above. This embodiment is preferably realized with emitter materials that emit red light.

The compounds according to general formulae (I) and (11) are suitable as single host material as well as host material, together with one or more further host materials (co-host). Suitable further host materials are mentioned below. “Further host materials” means in the sense of the present application, host materials different from the compounds of general formulae (I) and (11). However, it is also possible to use two or more different compounds of general formula (I) or (11) as host material in the light-emitting layer in an OLED of the present application.

In a more preferred embodiment, the light-emitting layer is formed from 0.1 to 70% by weight, preferably 1 to 30% by weight, of at least one of the aforementioned emitter materials and 30 to 99.9% by weight, preferably 70 to 99% by weight, of at least one of the matrix materials mentioned in the specification—in one embodiment at least one compound according to general formulae (I) and (11)—where the sum total of the emitter material and of the matrix material adds up to 100% by weight.

In a further more preferred embodiment, the light-emitting layer comprises a compound of general formula (I) or (11) as matrix material, at least one further matrix material (co-host) and at least one emitter material. In said embodiment, the light-emitting layer is formed from 0.1 to 70% by weight, preferably 1 to 30% by weight, of the at least one emitter material and 30 to 99.9% by weight, preferably 70 to 99% by weight, of a compound according to general formula (I) or (11) and the further matrix material, where the sum total of the at least one emitter material, the further matrix material and of the compound of general formula (I) or (11) adds up to 100% by weight.

The content ratio of the compound according to general formula (I) or (11) as first host material and the second matrix material as co-host in the light emitting layer is not particularly limited and may be selected accordingly, and the ratio of first host material:second host material is preferably 1:99 to 99:1, more preferably 10:90 to 90:10, each based on mass.

In the following host materials are mentioned that may be used in the electronic device according to the present invention as single host materials, if the compounds according to the present invention are used as charge transporting material, i.e. as electron transporting material or hole transporting material. The host materials that are mentioned in the following can also be used as second host materials, if the compounds according to general formula (I) or (11) are used as first host material and vice versa.

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, WO2008140114 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, JP2010114180 the compounds PH-1 to PH-36, US2009284138 the compounds 1 to 111 and H1 to H71, WO2008072596 the compounds 1 to 45, JP2010021336 the compounds H-1 to H38, 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, JP2009114369 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, WO2007119816 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 and European patent applications EP12175635.7, EP12185230.5 and EP12191408.9 (in particular page 25 to 29 of EP12191408.9).

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

Further suitable host materials, are described in WO2011137072 (for example,

best results are achieved if said compounds are combined with

WO2012048266 (for example,

The host materials mentioned above may be used in the OLED of the present invention alone or in combination with the compound of general formula (I) or (11) as host material. In this case, the compound of general formula (I) or (11) is the host and the host materials mentioned above are the co-hosts.

Further examples of the compounds which are suitable as phosphorescent host, alone or in combination with the compound of general formula (I) or (11) as host material, include a carbazole derivative, a triazole derivative, a oxazole derivative, an oxadiazole derivative, an imidazole derivative, a polyarylalkane derivative, a pyrazoline derivative, a pyrazolone derivative, a phenylenediamine derivative, an arylamine derivative, an amino-substituted chalcone derivative, a styrylanthracene derivative, a fluorenone derivative, a hydrazone derivative, a stilbene derivative, a silazane derivative, an aromatic tertiary amine compound, a styrylamine compound, an aromatic methylidene compound, a porphyrin compound, an anthraquinodimethane derivative, an anthrone derivative, a diphenylquinone derivative, a thiopyran dioxide derivative, a carbodiimide derivative, a fluorenylidenemethane derivative, a distyrylpyrazine derivative, a tetracarboxylic anhydride of fused ring such as naphthalene and perylene, a phthalocyanine derivative, a metal complex of 8-quinolinol derivative, metal phthalocyanine, metal complexes having a ligand such as benzoxazole and benzothiazole, an electroconductive oligomer, such as a polysilane compound, a poly(N-vinylcarbazole) derivative, an aniline copolymer, thiophene oligomer, and a polythiophene, and a polymer such as a polythiophene derivative, a polyphenylene derivative, a polyphenylenevinylene derivative, and a polyfluorene derivative. These phosphorescent hosts may be used alone or in combination of two or more. Specific examples thereof are shown below:

Further suitable hosts, which are especially useful as co-host together with at least one compound of formulae (I), (II) or (III) are the hosts described in US2014048784, US2012223295, US2014367667, US2013234119, US2014001446, US2014231794, US2014008633, WO2012108388, WO2014009317 and WO2012108389, as well as the compounds of formula (1) described in the EP application EP 15187954, filed on Oct. 1, 2015.

Especially preferred are the first and second host materials mentioned in US2013234119, the host materials mentioned in US2014048784 and the compounds of formula (1) described in the EP application EP 15187954, filed on Oct. 1, 2015.

The first host material mentioned in US2013234119 which is preferably used as co-host together with at least one compound of general formula (I) or (11) in the light emitting layer of an OLED according to the present invention is represented by formula (A). The lifetime of an OLED is increased by using as a first host material at least one compound of general formula (I) or (11) and as co-host the host material represented by formula (A) in the light emitting layer:

whereineach of A^1A and A^2A independently represents an aryl group having 6 to 30 ring carbon atoms, which may be unsubstituted or substituted; or a heterocyclic group having 5 to 30 ring atoms, which may be unsubstituted or substituted;A³A represents a divalent aryl group having 6 to 30 ring carbon atoms, which may be unsubstituted or substituted; or a divalent heterocyclic group having 5 to 30 ring atoms, which may be unsubstituted or substituted;mA represents an integer of 0 to 3;each of X^1A to X^8A and Y^1A to Y^8A independently represents N or CR^a;each of R^a independently represents a hydrogen atom, an aryl group having 6 to 30 ring carbon atoms, which may be unsubstituted or substituted; a heterocyclic group having 5 to 30 ring atoms, which may be unsubstituted or substituted; an alkyl group having 1 to 30 carbon atoms, which may be unsubstituted or substituted for example by E; a silyl group, which may be unsubstituted or substituted; a halogen atom, or a cyano group, provided that when two or more R^a groups exist, the R^a groups may be the same or different and one of X^5A to X^8A and one of Y^1A to Y^4A are bonded to each other via A³A; andthe formula (A) satisfies at least one of the flowing requirements (i) to (v);(i) at least one of A^1A and A^2A represents a cyano-substituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms or a cyano-substituted heterocyclic group having 5 to 30 ring atoms;(ii) at least one of X^1A to X^4A and Y^5A to Y^8A represents CR^a, and at least one of R^a in X^1A to X^4A and Y^5A to Y^8A represents a cyano-substituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms or a cyano-substituted heterocyclic group having 5 to 30 ring atoms;(iii) mA represents an integer of 1 to 3 and at least one of A³ represents a cyano-substituted divalent aromatic hydrocarbon group having 6 to 30 ring carbon atoms or a cyano-substituted divalent heterocyclic group having 5 to 30 ring atoms;(iv) at least one of X^5A to X^8A and Y^1A to Y^4A represents CR^a, and at least one of R^a in X^5A to X^8A and Y^1A to Y^4A represents a cyano-substituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms or a cyano-substituted heterocyclic group having 5 to 30 ring atoms; and(v) at least one of x^1A to X^8A and Y^1A to Y^8A represents C—CN.

The cyano-substituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms and the cyano-substituted heterocyclic group having 5 to 30 ring atoms may be further substituted by a group other than the cyano group.

The subscript mA is preferably 0 to 2 and more preferably 0 or 1. When mA is 0, one of X^5A to X^8A and one of Y^1A to Y^4A are bonded to each other via a single bond.

In formula (A), the groups mentioned above have the following meanings:

The aromatic hydrocarbon group having 6 to 30 ring carbon atoms represented by A^1A, A^2A and R^a may be a non-condensed aromatic hydrocarbon group or a condensed aromatic hydrocarbon group. Specific examples thereof include phenyl group, naphthyl group, phenanthryl group, biphenyl group, terphenyl group, quaterphenyl group, fluoranthenyl group, triphenylenyl group, phenanthrenyl group, fluorenyl group, spirofluorenyl group, 9,9-diphenylfluorenyl group, 9,9′-spirobi[9H-fluorene]-2-yl group, 9,9-dimethylfluorenyl group, benzo[c]phenanthrenyl group, benzo[a]triphenylenyl group, naphtho[1,2-c]phenanthrenyl group, naphtho[1,2-a]triphenylenyl group, dibenzo[a,c]triphenylenyl group, and benzo[b]fluoranthenyl group, with phenyl group, naphthyl group, biphenyl group, terphenyl group, phenanthryl group, triphenylenyl group, fluorenyl group, spirobifluorenyl group, and fluoranthenyl group being preferred, and phenyl group, 1-naphthyl group, 2-naphthyl group, biphenyl-2-yl group, biphenyl-3-yl group, biphenyl-4-yl group, phenanthrene-9-yl group, phenanthrene-3-yl group, phenanthrene-2-yl group, triphenylene-2-yl group, 9,9-dimethylfluorene-2-yl group, fluoranthene-3-yl group being more preferred.

Examples of the divalent aromatic hydrocarbon group having 6 to 30 ring carbon atoms represented by A^3A include divalent residues of the above aromatic hydrocarbon groups having 6 to 30 ring carbon atoms.

The heterocyclic group having 5 to 30 ring atoms represented by A^1A, A^2A and R^a may be a non-condensed heterocyclic group or a condensed heterocyclic group. Specific examples thereof include the residues of pyrrole ring, isoindole ring, benzofuran ring, isobenzofuran ring, dibenzothiophene ring, isoquinoline ring, quinoxaline ring, phenanthridine ring, phenanthroline ring, pyridine ring, pyrazine ring, pyrimidine ring, pyridazine ring, triazine ring, indole ring, quinoline ring, acridine ring, pyrrolidine ring, dioxane ring, piperidine ring, morpholine ring, piperazine ring, carbazole ring, furan ring, thiophene ring, oxazole ring, oxadiazole ring, benzoxazole ring, thiazole ring, thiadiazole ring, benzothiazole ring, triazole ring, imidazole ring, benzimidazole ring, pyran ring, dibenzofuran ring, and benzo[c]dibenzofuran ring, and the residues of derivatives of these rings, with the residues of dibenzofuran ring, carbazole ring, dibenzothiophene ring, and derivatives of these rings being preferred, and the residues of dibenzofuran-2-yl group, dibenzofuran-4-yl group, 9-phenylcarbazole-3-yl group, 9-phenylcarbazole-2-yl group, dibenzothiophene-2-yl group, and dibenzothiophene-4-yl group being more preferred.

Examples of the divalent heterocyclic group having 5 to 30 ring atoms represented by A³A include divalent residues of the above heterocyclic group having 5 to 30 ring atoms.

Examples of the alkyl group having 1 to 30 carbon atoms represented by R^a include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, n-nonyl group, n-decyl group, n-undecyl group, n-dodecyl group, n-tridecyl group, n-tetradecyl group, n-pentadecyl group, n-hexadecyl group, n-heptadecyl group, n-octadecyl group, neopentyl group, 1-methylpentyl group, cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cyclooctyl group, and adamantyl group, with methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, cyclopentyl group, and cyclohexyl group being preferred.

Examples of the silyl group, which may be unsubstituted or substituted; represented by R^a include trimethylsilyl group, triethylsilyl group, tributylsilyl group, dimethylethylsilyl group, t-butyldimethylsilyl group, vinyldimethylsilyl group, propyldimethylsilyl group, dimethylisopropylsilyl group, dimethylpropylsilyl group, dimethylbutylsilyl group, dimethyltertiarybutylsilyl group, diethylisopropylsilyl group, phenyldimethylsilyl group, diphenylmethylsilyl group, diphenyltertiarybutylsilyl group, and triphenylsilyl group, with trimethylsilyl group, triethylsilyl group, t-butyldimethylsilyl group, vinyldimethylsilyl group, and propyldimethylsilyl group being preferred.

Examples of the halogen atom represented by R^a include fluorine, chlorine, bromine, and iodine, with fluorine being preferred.

Also preferred as R^a is a hydrogen atom or an aryl group having 6 to 30 ring carbon atoms, which may be unsubstituted or substituted.

Examples of the optional substituent indicated by “substituted or unsubstituted” and “may be substituted” referred to above or hereinafter include a halogen atom (fluorine, chlorine, bromine, iodine), a cyano group, an alkyl group having 1 to 20, preferably 1 to 6 carbon atoms, a cycloalkyl group having 3 to 20, preferably 5 to 12 carbon atoms, an alkoxyl group having 1 to 20, preferably 1 to 5 carbon atoms, a haloalkyl group having 1 to 20, preferably 1 to 5 carbon atoms, a haloalkoxyl group having 1 to 20, preferably 1 to 5 carbon atoms, an alkylsilyl group having 1 to 10, preferably 1 to 5 carbon atoms, an aromatic hydrocarbon group having 6 to 30, preferably 6 to 18 ring carbon atoms, an aryloxy group having 6 to 30, preferably 6 to 18 ring carbon atoms, an arylsilyl group having 6 to 30, preferably 6 to 18 carbon atoms, an aralkyl group having 7 to 30, preferably 7 to 20 carbon atoms, and a heteroaryl group having 5 to 30, preferably 5 to 18 ring atoms.

The optional substituent mentioned above may be further substituted by the optional group mentioned above.

Examples of the optional alkyl group having 1 to 20 carbon atoms include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, n-nonyl group, n-decyl group, n-undecyl group, n-dodecyl group, n-tridecyl group, n-tetradecyl group, n-pentadecyl group, n-hexadecyl group, n-heptadecyl group, n-octadecyl group, neopentyl group, and 1-methylpentyl group.

Examples of the optional cycloalkyl group having 3 to 20 carbon atoms include cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cyclooctyl group, and adamantyl group.

Examples of the optional alkoxyl group having 1 to 20 carbon atoms include those having an alkyl portion selected from the alkyl groups mentioned above.

Examples of the optional haloalkyl group having 1 to 20 carbon atoms include the alkyl groups mentioned above wherein the hydrogen atoms thereof are partly or entirely substituted by halogen atoms.

Examples of the optional haloalkoxyl group having 1 to 20 carbon atoms include the alkoxyl group mentioned above wherein the hydrogen atoms thereof are partly or entirely substituted by halogen atoms.

Examples of the optional alkylsilyl group having 1 to 10 carbon atoms include trimethylsilyl group, triethylsilyl group, tributylsilyl group, dimethylethylsilyl group, t-butyldimethylsilyl group, vinyldimethylsilyl group, propyldimethylsilyl group, dimethylisopropylsilyl group, dimethylpropylsilyl group, dimethylbutylsilyl group, dimethyltertiarybutylsilyl group, and diethylisopropylsilyl group.

Examples of the optional aryl group having 6 to 30 ring carbon atoms include those selected from the aryl groups mentioned above with respect to A^1A, A^2A and R^a.

Examples of the optional aryloxy group having 6 to 30 ring carbon atoms include those having an aryl portion selected from the aromatic hydrocarbon groups mentioned above.

Examples of the optional arylsilyl group having 6 to 30 carbon atoms include phenyldimethylsilyl group, diphenylmethylsilyl group, diphenyltertiarybutylsilyl group, and triphenylsilyl group.

Examples of the optional aralkyl group having 7 to 30 carbon atoms include benzyl group, 2-phenylpropane-2-yl group, 1-phenylethyl group, 2-phenylethyl group, 1-phenylisopropyl group, 2-phenylisopropyl group, phenyl-t-butyl group, α-naphthylmethyl group, 1-α-naphthylethyl group, 2-α-naphthylethyl group, 1-α-naphthylisopropyl group, 2-α-naphthylisopropyl group, β-naphthylmethyl group, 1-β-naphthylethyl group, 2-β-naphthylethyl group, 1-β-naphthyl isopropyl group, 2-β-naphthylisopropyl group, 1-pyrrolylmethyl group, 2-(1-pyrrolyl)ethyl group, p-methylbenzyl group, m-methylbenzyl group, o-methylbenzyl group, p-chlorobenzyl group, m-chlorobenzyl group, o-chlorobenzyl group, p-bromobenzyl group, m-bromobenzyl group, o-bromobenzyl group, p-iodobenzyl group, m-iodobenzyl group, o-iodobenzyl group, p-hydroxybenzyl group, m-hydroxybenzyl group, o-hydroxybenzyl group, p-aminobenzyl group, m-aminobenzyl group, o-aminobenzyl group, p-nitrobenzyl group, m-nitrobenzyl group, o-nitrobenzyl group, p-cyanobenzyl group, m-cyanobenzyl group, o-cyanobenzyl group, 1-hydroxy-2-phenylisopropyl group, and 1-chloro-2-phenyl isopropyl group.

Examples of the optional heteroaryl group having 5 to 30 ring atoms include those selected from the heterocyclic groups mentioned above with respect to A^1A, A^2A and R^a.

The “carbon number of a to b” in the expression of “substituted or unsubstituted X group having carbon number of a to b” is the carbon number of the unsubstituted X group and does not include the carbon atom of the optional substituent.

The hydrogen atom referred to herein includes isotopes different from neutron numbers, i.e., light hydrogen (protium), heavy hydrogen (deuterium) and tritium.

In the host material represented by formula (A), the groups represented by formulae (a) and (b) are bonded to each other via -(A³)_mA- at one of X^5A to X^8A and one of Y^1A to Y^4A. Specific examples of the bonding manner between formulae (a) and (b) are represented by X^6A-(A^3A)_mA-Y^3A, X^6A-(A^3A)_mA-Y^2A, X^6A-(A^3A)_mA-Y^4A, X^6A-(A^3A)_mA-Y^1A, X^7A-(A^3A)_mA-Y^3A, X^5A-(A^3A)_mA-Y^3A, X^8A-(A^3A)_mA-Y^3A, X^7A-(A^3A)_mA-Y^2A, X^7A-(A^3A)_mA-Y^4A, X^7A-(A^3A)_mA-Y^1A, X^5A-(A^3A)_mA-Y^2A, X^8A-(A^3A)_mA-Y^2A, X^8A-(A^3A)_mA-Y^4A, X^8A-(A^3A)_mA-Y^1A, X^5A-(A^3A)_mA-Y^1A, and X^5A-(A^3A)_mA-Y^4A.

In preferred embodiments of the host material represented by formula (A), the bonding manner between formulae (a) and (b) are represented by X^6A-(A^3A)_mA-Y^3A, X^6A-(A^3A)_mA-Y^2A, or X^7A-(A^3A)_mA-Y^3A, namely the material for organic electroluminescence device is preferably represented by formula (XXII), (XXIII), or (XXIV):

wherein X^1A to X^8A, Y^1A to Y^8A, A^1A to A^3A, and mA are the same as X^1A to X^8A, Y^1A to Y^8A, A^1A to A^3A, mA in formula (A), and each of formulae (XXII), (XXIII), and (XXIV) satisfies at least one of the requirements (i) to (v) as specified in the definition of formula (A).

The host material represented by formula (A) satisfies at least one of the requirements (i) to (v), namely, the host material is a cyano group-introduced biscarbazole derivative having a group represented by formula (a) and a group represented by formula (b) which are linked to each other.

A³A of formula (A) preferably represents a single bond, a substituted or unsubstituted divalent monocyclic hydrocarbon group having 6 or less ring carbon atoms, or a substituted or unsubstituted divalent monocyclic heterocyclic group having 6 or less ring atoms.

Examples of the monocyclic hydrocarbon group having 6 or less ring carbon atoms represented by A^3A include phenylene group, cyclopentenylene group, cyclopentadienylene group, cyclohexylene group, and cyclopentylene group, with phenylene group being preferred.

Examples of the monocyclic heterocyclic group having 6 or less ring atoms represented by A^3A include pyrrolylene group, pyrazinylene group, pyridinylene group, furylene group, and thiophenylene group.

In a preferred embodiment of formulae (A), (XXII), (XXIII), and (XXIV), mA is 0 and one of X^5A to X^8A and one of Y^1A to Y^4A are bonded to each other via a single bond; or A³A represents the substituted or unsubstituted monocyclic hydrocarbon group having 6 or less ring carbon atoms or the substituted or unsubstituted monocyclic heterocyclic group having 6 or less ring atoms.

In more preferred embodiment, mA is 0 and one of X^5A to X^8A and one of Y^1A to Y^4A are bonded to each other via a single bond; or A³A represents a substituted or unsubstituted phenylene group.

The host material of formula (A) satisfies preferably at least one of the requirements (i) and (ii);

(i) at least one of A^1A and A^2A represents a cyano-substituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms or a cyano-substituted heterocyclic group having 5 to 30 ring atoms; and(ii) at least one of X^1A to X^4A and Y^5A to Y^8A represents CR^a, and at least one of R^a in X^1A to X^4A and Y^5A to Y^8A represents a cyano-substituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms or a cyano-substituted heterocyclic group having 5 to 30 ring atoms.

Namely, the host material of formula (A) is preferably any one of the compounds;

(1) satisfying the requirement (i), but not satisfying the requirements (ii) to (v);(2) satisfying the requirement (ii), but not satisfying the requirements (i) and (iii) to (v); and(3) satisfying both the requirements (i) and (ii), but not satisfying the requirements (iii) to (v).

The host material of formula (A) satisfying the requirement (i) and/or (ii) has a structure wherein the cyano group-containing aromatic hydrocarbon group or the cyano group-containing heterocyclic group is introduced to the terminal end of the central skeleton comprising the groups represented by formulae (a) and (b).

When the host material of formula (A) satisfies the requirement (i), at least one of A^1A and A^2A is preferably a cyano-substituted phenyl group, a cyano-substituted naphthyl group, a cyano-substituted phenanthryl group, a cyano-substituted dibenzofuranyl group, a cyano-substituted dibenzothiophenyl group, a cyano-substituted biphenyl group, a cyano-substituted terphenyl group, a cyano-substituted 9,9-diphenylfluorenyl group, a cyano-substituted 9,9′-spirobi[9H-fluorene]-2-yl group, a cyano-substituted 9,9′-dimethylfluorenyl group, or a cyano-substituted triphenylenyl group, and more preferably 3′-cyanobiphenyl-2-yl group, 3′-cyanobiphenyl-3-yl group, 3′-cyanobiphenyl-4-yl group, 4′-cyanobiphenyl-3-yl group, 4′-cyanobiphenyl-4-yl group, 4′-cyanobiphenyl-2-yl group, 6-cyanonaphthalene-2-yl group, 4-cyanonaphthalene-1-yl group, 7-cyanonaphthalene-2-yl group, 8-cyanodibenzofuran-2-yl group, 6-cyanodibenzofuran-4-yl group, 8-cyanodibenzothiophene-2-yl group, 6-cyanodibenzothiophene-4-yl group, 7-cyano-9-phenylcarbazole-2-yl group, 6-cyano-9-phenylcarbazole-3-yl group, 7-cyano-9,9-di methylfluorene-2-yl group, or 7-cyanotriphenylene-2-yl group.

The host material of formula (A) wherein A^1A is substituted by a cyano group and A^2A is not substituted by a cyano group is preferred. In this case, the first host material which does not satisfy the requirement (ii) is more preferred.

When the host material of formula (A) satisfies the requirement (ii), at least one of X^1A to X^4A and Y^5A to Y^8A is preferably CR^a, and one of R^a in X^1A to X^4A and Y^5A to Y^8A is preferably a cyano-substituted phenyl group, a cyano-substituted naphthyl group, a cyano-substituted phenanthryl group, a cyano-substituted dibenzofuranyl group, a cyano-substituted dibenzothiophenyl group, a cyano-substituted biphenyl group, a cyano-substituted terphenyl group, a cyano-substituted 9,9-diphenylfluorenyl group, a cyano-substituted 9,9′-spirobi[9H-fluorene]-2-yl group, a cyano-substituted 9,9′-dimethylfluorenyl group, or a cyano-substituted triphenylenyl group, and more preferably 3′-cyanobiphenyl-2-yl group, 3′-cyanobiphenyl-3-yl group, 3′-cyanobiphenyl-4-yl group, 4′-cyanobiphenyl-3-yl group, 4′-cyanobiphenyl-4-yl group, 4′-cyanobiphenyl-2-yl group, 6-cyanonaphthalene-2-yl group, 4-cyanonaphthalene-1-yl group, 7-cyanonaphthalene-2-yl group, 8-cyanodibenzofuran-2-yl group, 6-cyanodibenzofuran-4-yl group, 8-cyanodibenzothiophene-2-yl group, 6-cyanodibenzothiophene-4-yl group, 7-cyano-9-phenylcarbazole-2-yl group, 6-cyano-9-phenylcarbazole-3-yl group, 7-cyano-9,9-di methylfluorene-2-yl group, or 7-cyanotriphenylene-2-yl group.

It is preferred for the host material of formula (A) to satisfy the requirement (ii), but not satisfy the requirement (i).

In formulae (A) and (XXII) to (XXIV), A^1A and A^2A are preferably different from each other, and more preferably, A^1A is substituted by a cyano group but A^2A is not substituted by a cyano group. Namely, the host material of formula (A) is preferably structurally asymmetric.

The production method of the first host material is not particularly limited and it is produced according to a known method, for example, by a coupling reaction of a carbazole derivative and an aromatic halogenated compound in the presence of a copper catalyst described in Tetrahedron 40 (1984) 1435 to 1456 or a palladium catalyst described in Journal of American Chemical Society 123 (2001) 7727 to 7729.

Examples of the host material of formula (A) are mentioned in [0145] in US2013234119.

Examples for preferred host materials that are preferably used as co-hosts in the electronic device according to the present invention are mentioned in US2013234119, WO2012108388 and WO2014009317 are:

According to the present invention, the compounds according to general formulae (I) and (11) can also be used in combination with host materials that are called “second host materials” in US20130234119, see in particular paragraphs 0146 to 0195 of US20130234119. In addition these compounds according to paragraphs 0146 to 1095 of US20130234119 can also be used as single host material in the electronic device according to the present invention, for example for red emitter material or green emitter material, preferably for red emitter material. The use of compounds according to general formulae (I) and (11) according to the present invention in combination with host materials according to paragraphs 0146 to 0195 of US20130234119 as host material for green light emitting materials is preferred.

In particular, compounds according to the formula (1 a) can be used as host materials in the electronic device according to the present invention:

whereinZ¹ represents a ring structure fused to the side a and represented by formula (1-1) or (1-2), and Z² represents a ring structure fused to the side b and represented by formula (1-1) or (1-2), provided that at least one of Z¹, and Z² is represented by formula (1-1);M¹ represents a substituted or unsubstituted nitrogen-containing aromatic heteroring having 5 to 30 ring atoms;L¹ represents a single bond, a substituted or unsubstituted divalent aromatic hydrocarbon group having 6 to 30 ring carbon atoms, a substituted or unsubstituted divalent heterocyclic group having 5 to 30 ring atoms, a cycloalkylene group having 5 to 30 ring atoms, or a group in which the preceding groups are directly linked to each other; andk represents 1 or 2.

In formula (1-1), a side c is fused to the side a orb of formula (1). In formula (1-2), any one of sides d, e and f is fused to the side a orb of formula (1). In formulae (1-1) and (1-2), X¹¹ represents a sulfur atom, an oxygen atom, N—R¹⁹, or C(R²⁰)(R²¹); and each of R¹¹ to R²¹ independently represents a hydrogen atom, a heavy hydrogen atom, a halogen atom, a cyano group, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3 to 30 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted aryloxy group having 6 to 30 ring carbon atoms, provided that adjacent groups of R<11> to R<21> may be bonded to each other to form a ring.

The nitrogen-containing aromatic heteroring represented by M¹ of formula (1) includes an azine rings

Examples of the nitrogen-containing aromatic heteroring include pyridine, pyrimidine, pyrazine, triazine, aziridine, azaindolizine, indolizine, imidazole, indole, isoindole, indazole, purine, pteridine, β-carboline, naphthyridine, quinoxaline, terpyridine, bipyridine, acridine, phenanthroline, phenazine, and imidazopyridine, with pyridine, pyrimidine, and triazine being particularly preferred. The formula (1) is preferably represented by formula (2):

Z¹ represents a ring structure fused to the side a and represented by formula (1-1) or (1-2), and Z² represents a ring structure fused to the side b and represented by formula (1-1) or (1-2), provided that at least one of Z¹ and Z² is represented by formula (1-1);L¹ is as defined in formula (1);each of X¹² to X¹⁴ independently represents a nitrogen atom, CH, or a carbon atom bonded to R³¹ or L¹, provided that at least one of X¹² to X¹⁴ represents a nitrogen atom;each of Y¹¹ to Y¹³ independently represents CH or a carbon atom bonded to R³¹ or L¹;each of R³¹ independently represents a halogen atom, a cyano group, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3 to 30 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted aryloxy group having 6 to 30 ring carbon atoms;when two or more R³¹ groups exist, the R³¹ groups may be the same or different and adjacent R³¹ groups may be bonded to each other to form a ring;k represents 1 or 2, and n represents an integer of 0 to 4;the side c of formula (1-1) is fused to the side a orb of formula (2); and any one of sides d, e and f of formula (1-2) is fused to the side a or b of formula (2).

Examples of the compound wherein the ring represented by formula (1-1) or (1-2) is fused to the side a or b of formula (2) are shown below.

The compound represented by formula (1) or (2) is more preferably represented by formula (3) and particularly preferably represented by formula (4).

In formula (3), L¹ is as defined in formula (1);

each of X¹² to X¹⁴ independently represents a nitrogen atom, CH, or a carbon atom bonded to R³¹ or L¹, provided that at least one of X¹² to X¹⁴ represents a nitrogen atom;each of Y¹¹ to Y¹³ independently represents CH or a carbon atom bonded to R³¹ or L¹;each of R³¹ independently represents a halogen atom, a cyano group, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3 to 30 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted aryloxy group having 6 to 30 ring carbon atoms;when two or more R³¹ groups exist, the R³¹ groups may be the same or different and adjacent R³¹ groups may be bonded to each other to form a ring;n represents an integer of 0 to 4;each of R⁴¹ to R⁴⁸ independently represents a hydrogen atom, a heavy hydrogen atom, a halogen atom, a cyano group, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3 to 30 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted aryloxy group having 6 to 30 ring carbon atoms; andadjacent groups of R⁴¹ to R⁴⁸ may be bonded to each other to form a ring.

In formula (4), L¹ is as defined in formula (1);

each of X¹² to X¹⁴ independently represents a nitrogen atom, CH, or a carbon atom bonded to R³¹ or L¹, provided that at least one of X¹² to X¹⁴ represents a nitrogen atom;each of Y¹¹ to Y¹³ independently represents CH or a carbon atom bonded to R³¹ or L¹;each of R³¹ independently represents a halogen atom, a cyano group, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3 to 30 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted aryloxy group having 6 to 30 ring carbon atoms;adjacent R³¹ groups may be bonded to each other to form a ring;n represents an integer of 0 to 4;each of L² and L³ independently represents a single bond, a substituted or unsubstituted divalent aromatic hydrocarbon group having 6 to 30 ring carbon atoms, a substituted or unsubstituted divalent heterocyclic group having 5 to 30 ring atoms, a cycloalkylene group having 5 to 30 ring atoms, or a group in which the preceding groups are directly linked to each other;each of R⁵¹ to R⁵⁴ independently represents a halogen atom, a cyano group, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkylsilyl group having 3 to 30 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted aryloxy group having 6 to 30 ring carbon atoms;when two or more R⁵¹ groups exist, the R⁵¹ groups may be the same or different and adjacent R⁵¹ groups may be bonded to each other to form a ring;when two or more R⁵² groups exist, the R⁵² groups may be the same or different and adjacent R⁵² groups may be bonded to each other to form a ring;when two or more R⁵³ groups exist, the R⁵³ groups may be the same or different and adjacent R⁵³ groups may be bonded to each other to form a ring;when two or more R⁵⁴ groups exist, the R⁵⁴ groups may be the same or different and adjacent R⁵⁴ groups may be bonded to each other to form a ring;M² represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms or a substituted or unsubstituted heterocyclic group having 5 to 30 ring atoms; andeach of p and s independently represents an integer of 0 to 4, and each of q and r independently represents an integer of 0 to 3.

In formulae (1) to (4), (1-1), and (1-2), the groups represented by R¹¹ to R²¹, R³¹, R⁴¹ to R⁴⁸, and R⁵¹ to R⁵⁴ are as defined above with respect to formula (A).

Examples of the divalent aromatic hydrocarbon group having 6 to 30 ring carbon atoms and the divalent heterocyclic group having 5 to 30 ring atoms represented by L¹ to L³ of formulae (1) to (4) includes divalent residues of the corresponding groups described above with respect to formula (A).

According to a further preferred embodiment of the present invention, host materials according to US20140048784, in particular according to paragraphs 0098 to 0154 can be used in the electronic device according to the present invention, in particular, if red light emitting materials are used. The host materials according to US20140048784 can be used as single host materials, which can is preferred, or can be used in combination with compounds (I), (II) or (Ill) according to the present invention as host material and co-host:

The host material according to US2014048784 is a biscarbazole derivative, having two carbazole structures in a molecule thereof.

The biscarbazole derivative has, at a specific position, a substituted or unsubstituted fluoranthenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted benzophenanthrenyl group, a substituted or unsubstituted benzotriphenylenyl group, a substituted or unsubstituted dibenzotriphenylenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted benzochrysenyl group, a substituted or unsubstituted picenyl group, a substituted or unsubstituted benzo[b]fluoranthenyl group, a substituted or unsubstituted benzofuranyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted benzothiophenyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted binaphthyl group, a substituted or unsubstituted benzonaphthofuranyl group, a substituted or unsubstituted benzonaphthothiophenyl group, a substituted or unsubstituted dibenzophenanthrenyl group, a substituted or unsubstituted naphthotriphenylenyl group, a substituted or unsubstituted benzofluoranthenyl group, a substituted or unsubstituted benzofluorenyl group, or a substituted or unsubstituted phenyl group. Examples thereof include compounds represented by any of formulae (1) to (4), (1′), (1a), and (10).

wherein;each of A1 and A2 independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms;each of Y1 to Y16 independently represents C(R) or a nitrogen atom, and each of R groups independently represents a hydrogen atom, a substituent, or a valence bonded to a carbazole skeleton; andeach of L1 and L2 independently represents a single bond, a substituted or unsubstituted, divalent aromatic hydrocarbon group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted, divalent aromatic heterocyclic group having 2 to 30 ring carbon atoms, provided that;at least one of A1, A2 and R represents a substituted or unsubstituted fluoranthenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted benzophenanthrenyl group, a substituted or unsubstituted benzotriphenylenyl group, a substituted or unsubstituted dibenzotriphenylenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted benzochrysenyl group, a substituted or unsubstituted picenyl group, a substituted or unsubstituted benzo[b]fluoranthenyl group, a substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted binaphthyl group, a substituted or unsubstituted dibenzophenanthrenyl group, a substituted or unsubstituted naphthotriphenylenyl group, a substituted or unsubstituted benzofluorenyl group, or a naphthyl group;when Y1 to Y16 all represent C(R) wherein R is a hydrogen atom, Y6 and Y11 are bonded to each other via a single bond, each of L1 and L2 represents a single bond, and A1 represents a phenanthrenyl group, A2 represents a phenyl group, a biphenylyl group, or a naphthyl group; andwhen Y1 to Y16 all represent C(R) wherein R is a hydrogen atom, Y6 and Y11 are bonded to each other via a single bond, each of L1 and L2 represents a single bond, and A1 represents a naphthyl group, A1 and A2 are different from each other.

In formulae (1) and (1′), at least one of Y1 to Y4 represents C(R), at least one of Y5 to Y8 represents C(R), at least one of Y9 to Y12 represents C(R), and at least one of Y13 to Y16 represent C(R).

In addition, at least one of Y5 to Y8 represents C(R) and at least one of Y9 to Y12 represents C(R), wherein two R groups represent valences which are bonded to each other.

The R groups in formulae (1) and (1′) may be the same or different.

In formula (1a), at least one of Y1a to Y4a represents C(R), at least one of Y5a to Y8a represents C(R), at least one of Y9a Y12a represents C(R), and at least one of Y13a to Y16a represents C(R).

In addition, at least one of Y5a to Y8a represents C(R) and at least one of Y9a to Y12a represents C(R), wherein two R groups represent valences which are bonded to each other.

The R groups in formula (1a) may be the same or different.

In formula (10), at least one of Y1′ to Y4′ represents C(R′), at least one of Y5′ to Y8′ represents C(R′), at least one of Y9′ to Y12′ represents C(R′), and at least one of Y13′ to Y16′ represents C(R′).

In addition, at least one of Y5′ to Y8′ represents C(R′) and at least one of Y9′ to Y12′ represents C(R′), wherein two R′ groups represent valences which are bonded to each other.

The R′ groups in formula (10) may be the same or different.

wherein each of A1, A2, Y1 to Y16, L1, and L2 in formulae (2) to (4) is as defined in formula (1).

wherein:each of A1 and A2 independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms or a substituted or unsubstituted aromatic heterocyclic group having 2 to 30 ring carbon atoms;each of Y1 to Y16 independently represents C(R) or a nitrogen atom, and each of R groups independently represents a hydrogen atom, a substituent, or a valence bonded to a carbazole skeleton; andeach of L1 and L2 independently represents a single bond, a substituted or unsubstituted, divalent aromatic hydrocarbon group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted, divalent aromatic heterocyclic group having 2 to 30 ring carbon atoms, provided that:at least one of A1, A2 and R represents a substituted or unsubstituted fluoranthenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted benzophenanthrenyl group, a substituted or unsubstituted benzotriphenylenyl group, a substituted or unsubstituted dibenzotriphenylenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted benzochrysenyl group, a substituted or unsubstituted picenyl group, a substituted or unsubstituted benzo[b]fluoranthenyl group, a substituted or unsubstituted benzofuranyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted benzothiophenyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted binaphthyl group, a substituted or unsubstituted benzonaphthofuranyl group, a substituted or unsubstituted benzonaphthothiophenyl group, a substituted or unsubstituted dibenzophenanthrenyl group, a substituted or unsubstituted naphthotriphenylenyl group, a substituted or unsubstituted benzofluorenyl group, or a substituted or unsubstituted phenyl group;when Y1 to Y16 all represent C(R) wherein R is a hydrogen atom, Y6 and Y11 are bonded to each other via a single bond, each of L1 and L2 represents a single bond, and A1 represents a phenanthrenyl group, A2 does not represent a phenanthrenyl group;when Y1 to Y16 all represent C(R), Y6 and Y11 are bonded to each other via a single bond, and each of L1 and L2 represents a single bond, each of R groups does not represent a fluorenyl group; andwhen A1 represents a fluorenyl group, A2 does not represent a phenyl group, a naphthyl group, or a fluorenyl group.

wherein:one of A1a and A2a represents a group represented by formula (a) and the other represents a substituted or unsubstituted fluoranthenyl group, a substituted or unsubstituted benzophenanthrenyl group, a substituted or unsubstituted picenyl group, a substituted or unsubstituted benzo[b]fluoranthenyl group, a substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted binaphthyl group, a substituted or unsubstituted dibenzophenanthrenyl group, a substituted or unsubstituted naphthotriphenylenyl group, or a substituted or unsubstituted benzofluorenyl group;each of Y1a to Y16a independently represents C(R) or a nitrogen atom, and each of R groups independently represents a hydrogen atom, a substituent, or a valence bonded to a carbazole skeleton;each of L1a and L2a independently represents a single bond, a substituted or unsubstituted, divalent aromatic hydrocarbon group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted, divalent aromatic heterocyclic group having 2 to 30 ring carbon atoms:

wherein each of Y21 and Y25 independently represents C(R^a) or a nitrogen atom, and each of R^a groups independently represents a hydrogen atom or a substituent.

The details of A1a, A2a, Y1a to Y16a, L1a, L2a, and R^a in formulae (1a) and (a) are the same as those of A1, A2, Y1 to Y16, L1, L2, and R in formula (1).

When one of A1a and A2a represents a group represented by formula (a) and the other represents a group including a large molecular weight fused ring, such as a triphenylenyl group and a chrysenyl group, the compound represented by formula (1a) has an excessively large molecular weight, increasing the vapor deposition temperature and therefore likely to increase the amount of thermally decomposed components. Therefore, when one of A1a and A2a represents a group represented by formula (a), the other preferably represents a substituted or unsubstituted fluoranthenyl group or a substituted or unsubstituted phenanthrenyl group.

wherein:one of A1′ and A2′ represents a substituted or unsubstituted naphthyl group or a substituted or unsubstituted fluorenyl group and the other represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms;each of Y1′ to Y16′ independently represents C(R′) or a nitrogen atom, and each of R′ groups independently represents a hydrogen atom, a substituent, or a valence bonded to a carbazole skeleton; andeach of L1′ and L2′ independently represents a single bond, a substituted or unsubstituted, divalent aromatic hydrocarbon group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted, divalent aromatic heterocyclic group having 2 to 30 ring carbon atoms.

The details of A1′, A2′, L1′, L2′, Y1′ to Y16′, and R′ in formula (10) are the same as those of A1, A2, L1, L2, Y1 to Y16, and R in formula (1).

In formulae (1) to (4) and (1′), at least one of A1, A2 and R preferably represents a substituted or unsubstituted fluoranthenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted benzophenanthrenyl group, a substituted or unsubstituted benzotriphenylenyl group, a substituted or unsubstituted dibenzotriphenylenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted benzochrysenyl group, a substituted or unsubstituted picenyl group, a substituted or unsubstituted benzo[b]fluoranthenyl group, a substituted or unsubstituted benzofuranyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted benzothiophenyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted fluorenyl group, or a substituted or unsubstituted binaphthyl group, because these groups are moderately bulky. More preferably, at least one of A1 and A2 represents a substituted or unsubstituted fluoranthenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted benzophenanthrenyl group, a substituted or unsubstituted benzotriphenylenyl group, a substituted or unsubstituted dibenzotriphenylenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted benzochrysenyl group, a substituted or unsubstituted picenyl group, a substituted or unsubstituted benzo[b]fluoranthenyl group, a substituted or unsubstituted benzofuranyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted benzothiophenyl group, a substituted or unsubstituted dibenzothiophenyl group, or a substituted or unsubstituted binaphthyl group.

Also preferably, each of A1 and A2 in formulae (1) to (4) and (1′) independently represents a substituted or unsubstituted fluoranthenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted benzotriphenylenyl group, a substituted or unsubstituted benzophenanthrenyl group, a substituted or unsubstituted dibenzofuranyl group, or a substituted or unsubstituted dibenzothiophenyl group.

In addition, -L1-A1 and -L2-A2 in formulae (1) to (4) and (1′) are preferably different from each other.

The substituted or unsubstituted phenyl group for any of A1, A2 and R is preferably a phenyl group substituted by an aromatic hydrocarbon group having 10 to 30 ring carbon atoms and particularly preferably a naphthylphenyl group.

When at least one of A1 and A2 in formulae (1) to (4) and (1′) represents a group represented by formula (a), the biscarbazole derivative is particularly preferred as a host material to be used in combination with a green emitting dopant.

In formula (a), Y21 and/or Y25 preferably represents a nitrogen atom, and each of Y22 and Y24 more preferably represents C(R^a).

Specific examples of the substituent which A1 and A2 in formulae (1) to (4) and (1′) may have and the substituents represented by R and R^a include a fluorine atom; a cyano group; a substituted or unsubstituted, linear, branched, or cyclic alkyl group having 1 to 20 carbon atoms; a linear, branched, or cyclic alkylene group having 1 to 20 carbon atoms; a linear, branched, or cyclic, divalent, unsaturated hydrocarbon group having 1 to 20 carbon atoms; a substituted or unsubstituted, linear, branched, or cyclic alkoxy group having 1 to 20 carbon atoms; a substituted or unsubstituted, linear, branched, or cyclic haloalkyl group having 1 to 20 carbon atoms; a substituted or unsubstituted, linear, branched, or cyclic haloalkoxy group having 1 to 20 carbon atoms; a substituted or unsubstituted, linear, branched, or cyclic alkylsilyl group having 1 to 10 carbon atoms; a substituted or unsubstituted arylsilyl group having 6 to 30 carbon atoms; a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 ring carbon atoms; and a substituted or unsubstituted aromatic heterocyclic group having 2 to 30 ring carbon atoms. In addition, a plurality of substituents of any such kind may exist, and when the plurality of substituents exist, the substituents may be the same or different from each other.

The R groups on adjacent ring carbon atoms may be bonded to each other to form a ring structure together with the ring carbon atoms.

Examples of the linear, branched, or cyclic alkyl group having 1 to 20 carbon atoms include a methyl group, an ethyl group, a propyl group, an isopropyl group, a n-butyl group, a s-butyl group, an isobutyl group, a t-butyl group, a n-pentyl group, a n-hexyl group, a n-heptyl group, a n-octyl group, a n-nonyl group, a n-decyl group, a n-undecyl group, a n-dodecyl group, a n-tridecyl group, a n-tetradecyl group, a n-pentadecyl group, a n-hexadecyl group, a n-heptadecyl group, a n-octadecyl group, a neopentyl group, a 1-methylpentyl group, a 2-methylpentyl group, a 1-pentylhexyl group, a 1-butylpentyl group, a 1-heptyloctyl group, a 3-methylpentyl group, a cyclopentyl group, a cyclohexyl group, a cyclooctyl group, a 3,5-tetramethylcyclohexyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, and a 1,1,1,3,3,3-hexafluoro-2-propyl group.

Examples of the linear, branched, or cyclic alkylene group having 1 to 20 carbon atoms include an ethylene group, a propylene group, and a butylene group.

Examples of the linear, branched, or cyclic, divalent unsaturated hydrocarbon group having 1 to 20 carbon atoms include a 1,3-butadiene-1,4-diylgroup.

Examples of the linear, branched, or cyclic alkylsilyl group having 1 to 10 carbon atoms include a trimethylsilyl group, a triethylsilyl group, a tributylsilyl group, a dimethylethylsilyl group, a dimethylisopropylsilyl group, a dimethylpropylsilyl group, a dimethylbutylsilyl group, a dimethyl-t-butylsilyl group, and a diethylisopropylsilyl group.

Examples of the arylsilyl group having 6 to 30 carbon atoms include a phenyldimethylsilyl group, a diphenylmethylsilyl group, a diphenyl-t-butylsilyl group, and a triphenylsilyl group.

Examples of the halogen atom include a fluorine atom.

Examples of the aromatic heterocyclic group having 2 to 30 ring carbon atoms include non-fused aromatic heterocyclic and fused aromatic heterocyclic groups, more specifically, a pyrrolyl group, a pyrazinyl group, a pyridinyl group, an indolyl group, an isoindolyl group, a furyl group, a benzofuranyl group, an isobenzofuranyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a quinolyl group, an isoquinolyl group, a quinoxalinyl group, a carbazolyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a thienyl group, and residues of a pyridine ring, a pyrazine ring, a pyrimidine ring, a pyridazine ring, a triazine ring, an indole ring, a quinoline ring, an acridine ring, a pyrrolidine ring, a dioxane ring, a piperidine ring, a morpholine ring, a piperazine ring, a carbazole ring, a furan ring, a thiophene ring, an oxazole ring, an oxadiazole ring, a benzoxazole ring, a thiazole ring, a thiadiazole ring, a benzothiazole ring, a triazole ring, an imidazole ring, a benzimidazole ring, a pyran ring, a dibenzofuran ring, and a benzo[c]dibenzofuran ring.

Examples of the aromatic hydrocarbon group having 6 to 30 ring carbon atoms include non-fused aromatic hydrocarbon groups and fused aromatic hydrocarbon groups, more specifically, a phenyl group, a naphthyl group, a phenanthryl group, a biphenyl group, a terphenyl group, a quaterphenyl group, a fluoranthenyl group, a triphenylenyl group, a phenanthrenyl group, a 9,9-dimethylfluorenyl group, a benzo[c]phenanthrenyl group, a benzo[a]triphenylenyl group, a naphtho[1,2-c]phenanthrenyl group, a naphtho[1,2-a]triphenylenyl group, a dibenzo[a,c]triphenylenyl group, and a benzo[b]fluoranthenyl group.

Examples of the divalent linking group represented by L1 and L2 in formulae (1) to (4) and (1′) include a substituted or unsubstituted, divalent aromatic hydrocarbon group having 6 to 30 ring carbon atoms and a substituted or unsubstituted, divalent aromatic heterocyclic group having 2 to 30 ring carbon atoms.

Examples of the divalent aromatic hydrocarbon group having 6 to 30 ring carbon atoms include groups obtained by making the examples of the aromatic hydrocarbon group having 6 to 30 ring carbon atoms mentioned above into divalent groups.

In addition, specific examples of the divalent aromatic heterocyclic group having 2 to 30 ring carbon atoms include groups obtained by making the examples of the aromatic heterocyclic group having 2 to 30 ring carbon atoms mentioned above into divalent groups.

In each of formulae (1) to (4) and (1′), Y1 to Y16 all preferably represent C(R).

In each of formulae (1) to (4) and (1′), the number of substituents represented by R in Y1 to Y8 or in Y9 to Y16 is preferably 0 to 2, more preferably 0 or 1.

Specific examples of the biscarbazole derivative represented by any one of formulae (1) to (4), (1′), and (10) include the following compounds. In the following structural formulae, D represents a heavy hydrogen (deuterium).

According to the present invention, the compounds according to general formulae (I) and (11) are preferably be used as host material in the light emitting layer of the electronic device, preferably in a OLED, according to the present invention. The compounds according to general formulae (I) and (11) can be used (a) as single host materials or can be used (b) in combination with any compounds suitable as host materials as mentioned above. Embodiment (a) is preferred; if a red light emitting material is present in the light emitting layer. Embodiment (b) is preferred; if a green light emitting material is present in the light emitting layer.

Preferred host materials, which may be used, if blue dopants are present in the light emitting layer, are mentioned in US 2012/112169. Preferably, the anthracene derivative represented by the formula (5) is used as host material for blue dopants:

In the formula (5), Ar¹¹ and Ar¹² are independently a substituted or unsubstituted monocyclic group having 5 to 50 ring atoms, a substituted or unsubstituted fused ring group having 8 to 50 ring atoms, or a group formed by combination of a monocyclic group and a fused ring group and R¹⁰¹ to R¹⁰⁸ are independently a group selected from a hydrogen atom, a substituted or unsubstituted monocyclic group having 5 to 50 ring atoms, a substituted or unsubstituted fused ring group having 8 to 50 ring atoms, a group formed by combination of a monocyclic group and a fused ring group, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 50 carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 50 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 50 ring carbon atoms, a substituted or unsubstituted silyl group, a halogen atom and a cyano group.

The monocyclic group in the formula (5) means a group which is composed only of ring structures having no fused structure.

As specific examples of the monocyclic group having 5 to 50 (preferably 5 to 30, more preferably 5 to 20) ring atoms, aromatic groups such as a phenyl group, biphenyl group, terphenyl group and quaterphenyl group, and heterocyclic groups such as a pyridyl group, pyradyl group, pyrimidyl group, triadinyl group, furyl group and thienyl group, can be given preferably.

Among these, a phenyl group, biphenyl group or terphenyl group is preferable.

The fused ring group in the formula (5) means a group formed by fusion of 2 or more ring structures.

As specific examples of the fused ring group having 8 to 50 (preferably 8 to 30, more preferably 8 to 20) ring atoms, fused aromatic ring groups such as a naphthyl group, phenanthryl group, anthryl group, chrysenyl group, benzanthryl group, benzophenanthryl group, triphenylenyl group, benzochrysenyl group, indenyl group, fluorenyl group, 9,9-dimethylfluorenyl group, benzofluorenyl group, dibenzofluorenyl group, fluoranthenyl group and benzofluoranthenyl group, and fused heterocyclic groups such as a benzofuranyl group, benzothiophenyl group, indolyl group, dibenzofuranyl group, dibenzothiophenyl group, carbazolyl group, quinolyl group and phenanthrolinyl group, can be given preferably.

Among these, a naphthyl group, phenanthryl group, anthryl group, 9,9-dimethylfluorenyl group, fluoranthenyl group, benzanthryl group, dibenzothiophenyl group, dibenzofuranyl group or carbazolyl group is preferable.

As preferable substituents of “substituted or unsubstituted . . . ” in Ar¹¹, Ar¹², and R¹⁰¹ to R¹⁰⁸, a monocyclic group, fused ring group, alkyl group, cycloalkyl group, silyl group, alkoxy group, cyano group and halogen atom (in particular, fluorine) can be given. A monocyclic group and fused ring group are particularly preferable.

It is preferred that the anthracene derivative represented by the formula (5) be any of the following anthracene derivatives (A), (B) and (C), which is selected depending on the constitution or demanded properties of an organic EL device to which it is applied.

(Anthracene Derivative (A))

This anthracene derivative is derivatives of the formula (5) wherein Ar¹¹ and Ar¹² are independently a substituted or unsubstituted fused ring group having 8 to 50 ring atoms. This anthracene derivative can be classified into the case that Ar¹¹ and Ar¹² are the same substituted or unsubstituted fused ring group and the case that Ar¹¹ and Ar¹² are different substituted or unsubstituted fused ring groups.

Particularly preferred is the anthracene derivative of the formula (5) wherein Ar¹¹ and Ar¹² are different (including difference in substituted positions) substituted or unsubstituted fused ring groups. Preferable specific examples of the fused ring are the same as those described above. Among those, a naphthyl group, phenanthryl group, benzanthryl group, 9,9-dimethylfluorenyl group and dibenzofuranyl group are preferable.

(Anthracene Derivative (B))

This anthracene derivative is derivatives of the formula (5) wherein one of Ar¹¹ and Ar¹² is a substituted or unsubstituted monocyclic group having 5 to 50 ring atoms, and the other is a substituted or unsubstituted fused ring group having 8 to 50 ring atoms.

As a preferred embodiment, Ar¹² is a naphthyl group, phenanthryl group, benzanthryl group, 9,9-dimethylfluorenyl group or dibenzofuranyl group, and Ar¹¹ is a phenyl group substituted by a monocyclic group or fused ring group.

As another preferred embodiment, Ar¹² is a fused ring group, and A¹¹ is an unsubstituted phenyl group. In this case, as the fused ring group, a phenanthryl group, 9,9-dimethylfluorenyl group, dibenzofuranyl group and benzoanthryl group are particularly preferable.

(Anthracene Derivative (C))

This anthracene derivative is derivatives of formula (5) wherein Ar¹¹ and Ar¹² are independently a substituted or unsubstituted monocyclic group having 5 to 50 ring atoms.

As a preferred embodiment, both Ar¹¹ and Ar¹² are a substituted or unsubstituted phenyl group.

As a further preferred embodiment, Ar¹¹ is an unsubstituted phenyl group, and Ar¹² is a phenyl group having a monocyclic group or a fused ring group as a substituent, and Ar¹¹ and Ar¹² are independently a phenyl group having a monocyclic group or a fused ring group as a substituent.

The preferable specific examples of the monocyclic group and fused ring group as a substituent are the same as those described above. As the monocyclic group as a substituent, a phenyl group and biphenyl group are further preferable. As the fused ring group as a substituent, a naphthyl group, phenanthryl group, 9,9-dimethylfluorenyl group, dibenzofuranyl group and benzanthryl group are further preferable.

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.

According to one embodiment of the present invention, at least one compound according to general formulae (I) and (11) is present in the hole/exciton blocking layer.

Additional 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(III) (BAlq), 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)-1H-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, disilylbenzophospholes, 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.

The compound according to general formula (I) or (11) according to the present invention is suitable as electron transport material, either alone or in combination with one or more of the electron transport materials mentioned below. The compound according to general formula (I) or (11) according to the present invention is preferably suitable as electron transport material, if a blue fluorescent emitter is present in the emitting layer.

Further suitable electron-transporting materials for layer (g) of the inventive OLEDs, which may be used in combination with the compound of general formula (I) or (11) according to the present invention or in absence of the compound of general formula (I) or (11) according to the present invention as electron transport material, 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).

Further suitable electron transport materials, which may be used in combination with the compound of general formula (I) or (11) according to the present invention or in absence of the compound of general formula (I) or (11) according to the present invention as electron transport material, are mentioned in Abhishek P. Kulkarni, Christopher J. Tonzola, Amit Babel, and Samson A. Jenekhe, Chem. Mater. 2004, 16, 4556-4573; G. Hughes, M. R. Bryce, J. Mater. Chem. 2005, 15, 94-107 and Yasuhiko Shirota and Hiroshi Kageyama, Chem. Rev. 2007, 107, 953-1010 (ETM, HTM).

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 (XVI) below, preferably a compound of the formula (XVIa) below. More preferably, in mixed electron-transport layers, in addition to at least one phenanthroline compound, alkaline earth metal or alkali metal hydroxyquinolate complexes, for example Liq, are used. Suitable alkaline earth metal or alkali metal hydroxyquinolate complexes are specified below (formula XVII). 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 Jul. 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 Jun. 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, for example 8-hydroxyquinolatolithium (Liq), and with Y, Ce, Sm, Gd, Tb, Er, Tm, Yb, Li₃N, Rb₂CO₃, 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 (XVII)

in whichR^32′ and R^33′ are each independently F, C₁-C₈-alkyl, or C₆-C₁₄-aryl, which is optionally substituted by one or more C₁-C₈-alkyl groups, ortwo R^32′ and/or R^33′ substituents together form a fused benzene ring which is optionally substituted by one or more C₁-C₈-alkyl groups;a and b are each independently 0, or 1, 2 or 3,M¹ is an alkaline metal atom or alkaline earth metal atom,p is 1 when M¹ is an alkali metal atom, p is 2 when M¹ is an earth alkali metal atom.

A very particularly preferred compound of the formula (XVII) is

(Liq), which may be present as a single species, or in other forms such as Li_gQ_g in which g is an integer, for example Li₆Q₆. 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 formula (XVI),

in which R^34″, R^35″, R^36″, R^37″, R^34′, R^35′, R^36′ and R^37′ are each independently H, C₁-C₁₈-alkyl, C₁-C₁₈-alkyl which is substituted by E′ and/or interrupted by D′, C₆-C₂₄-aryl, C₆-C₂₄-aryl which is substituted by G′, C₂-C₂₀-heteroaryl or C₂-C₂₀-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—; —O—; —NR^40′—; —SiR^45′R^46′—; —POR^47′—; —CR^38′═CR^39′—; or —C≡C—;E′ is —OR^44′; —SR^44′; —NR^40′R^41′; —COR^43′; —COOR^42′; —CONR^40′R^41′; —CN; or F;G′ is E′, C₁-C₁₈-alkyl, C₁-C₁₈-alkyl which is interrupted by D′, C₁-C₁₈-perfluoroalkyl, C₁-C₁₈-alkoxy, or C₁-C₁₈-alkoxy which is substituted by E′ and/or interrupted by D′, in whichR^38′ and R^39′ are each independently H, C₆-C₁₈-aryl; C₆-C₁₈-aryl which is substituted by C₁-C₁₈-alkyl or C₁-C₁₈-alkoxy; C₁-C₁₈-alkyl; or C₁-C₁₈-alkyl which is interrupted by —O—;R^40′ and R^41′ are each independently C₆-C₁₈-aryl; C₆-C₁₈-aryl which is substituted by C₁-C₁₈-alkyl or C₁-C₁₈-alkoxy; C₁-C₁₈-alkyl; or C₁-C₁₈-alkyl which is interrupted by —O—; orR^40′ and R^41′ together form a 6-membered ring;R^42′ and R^43′ are each independently C₆-C₁₈-aryl; C₆-C₁₈-aryl which is substituted by C₁-C₁₈-alkyl or C₁-C₁₈-alkoxy; C₁-C₁₈-alkyl; or C₁-C₁₈-alkyl which is interrupted by —O—,R^44′ is C₆-C₁₈-aryl; C₆-C₁₈-aryl which is substituted by C₁-C₁₈-alkyl or C₁-C₁₈-alkoxy; C₁-C₁₈-alkyl; or C₁-C₁₈-alkyl which is interrupted by —O—,R^45′ and R^46′ are each independently C₁-C₁₈-alkyl, C₆-C₁₈-aryl or C₆-C₁₈-aryl which is substituted by C₁-C₁₈-alkyl,R^47′ is C₁-C₁₈-alkyl, C₆-C₁₈-aryl or C₆-C₁₈-aryl which is substituted by C₁-C₁₈-alkyl.

Preferred compounds of the formula (XVI) are compounds of the formula (XVIa)

in which Q is:

R^48′ is H or C₁-C₁₈-alkyl andR⁴⁸″ is H, C₁-C₁₈-alkyl or

Particular preference is given to a compound of the formula

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 at least one compound of the formula (XVII) in an amount of 99 to 1% by weight, preferably 75 to 25% by weight, more preferably about 50% by weight, and at least one compound of the formula (XVI) in an amount of 1 to 99% by weight, preferably 25 to 75% by weight, more preferably about 50% by weight, where the amount of the compounds of the formulae (XVII) and the amount of the compounds of the formulae (XVI) adds up to a total of 100% by weight.

The preparation of the compounds of the formula (XVI) is described in J. Kido et al., Chem. Commun. (2008) 5821-5823, J. Kido et al., Chem. Mater. 20 (2008) 5951-5953 and J P2008/127326, 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, and at least one dibenzofuran compound in an amount of 1 to 99% by weight, preferably 25 to 75% 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 phenanthroline derivative and/or pyridine derivative.

In a further preferred embodiment, the electron-transport layer comprises at least one phenanthroline 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 WO2012/111462, WO2012/147397, WO2012014621, such as, for example, a compound of formula

US2012/0261654, such as, for example, a compound of formula

and WO2012/115034, such as for example, such as, for example, a compound of formula

Further preferred embodiments of the electron injection layer of the OLED according to the present invention are mentioned in US 2013306955.

For example, the electron transporting material that may be present in the electron transporting layer of the OLED according to the present invention is an electron transporting material represented by formula (1):

A1(L1-L2-L3-L4-Ar1)m  (1)

wherein:each of L1, L2, L3, and L4 independently represents a single bond, a substituted or unsubstituted alkylene group having 1 to 50 carbon atoms, a substituted or unsubstituted alkenylene group having 1 to 50 carbon atoms, a substituted or unsubstituted alkynylene group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkylene group having 3 to 50 ring carbon atoms, a substituted or unsubstituted arylene group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted heteroarylene group having 5 to 30 ring atoms;Ar1 represents a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms;A1 represents an m-valent residue of a ring-containing compound represented by formula (2); andm represents an integer of 1 or more:

wherein:ring X is a substituted or unsubstituted, saturated or unsaturated 5- to 8-membered ring having a ring nitrogen atom and a ring carbon atom;the ring X may be fused to one or more rings Y; andthe ring Y represents a substituted or unsubstituted hydrocarbon ring or a substituted or unsubstituted heteroring.

The ring Y preferably represents a substituted or unsubstituted non-fused aromatic hydrocarbon ring having 6 to 30 ring carbon atoms, a substituted or unsubstituted fused aromatic hydrocarbon ring having 10 to 30 ring carbon atoms, a substituted or unsubstituted non-fused heteroring having 5 to 30 ring atoms, or a substituted or unsubstituted fused heteroring having 10 to 30 ring atoms.

The electron transporting material of the invention is preferably represented by formula (1-1) or (1-2):

A11(-L11-L21-L31-L41Ar11)p  (1-1)

wherein:each of L11, L21, L31, and L41 independently represents a single bond, a substituted or unsubstituted alkylene group having 1 to 50 carbon atoms, a substituted or unsubstituted alkenylene group having 1 to 50 carbon atoms, a substituted or unsubstituted alkynylene group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkylene group having 3 to 50 ring carbon atoms, a substituted or unsubstituted arylene group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted heteroarylene group having 5 to 30 ring atoms;

Ar11 represents a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, or a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms;

A11 represents a p-valent residue of a ring-containing compound represented by formula (2-1); and

p represents an integer of 1 or more:

wherein;each of R¹ to R⁴ independently represents a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 50 carbon atoms, a substituted or unsubstituted alkoxycarbonyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms, a substituted or unsubstituted alkylsilyl group having 1 to 50 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted haloalkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkenyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkynyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkylamino group having 1 to 50 carbon atoms, a substituted or unsubstituted arylamino group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heteroarylamino group having 5 to 30 ring atoms, a substituted or unsubstituted acylamino group having 2 to 50 carbon atoms, a substituted or unsubstituted heteroaryloxy group having 5 to 30 ring atoms, a substituted or unsubstituted acyl group having 2 to 50 carbon atoms, a substituted or unsubstituted aryloxycarbonyl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted alkylcarbonyl group having 1 to 50 carbon atoms, a mercapto group, a substituted or unsubstituted alkylthio group having 1 to 50 carbon atoms, a substituted or unsubstituted arylthio group having 6 to 30 ring carbon atoms, a sulfonyl group, a boryl group, a phosphino group, an amino group, a halogen atom, a cyano group, a nitro group, a hydroxyl group, a carboxyl group, or a valence bonded to L11; or a pair of R¹ and R², R² and R³, or R³ and R⁴ are bonded to each other to form a ring Y represented by a substituted or unsubstituted hydrocarbon ring or a substituted or unsubstituted heteroring.

A11 of formula (1-1) preferably represents a p-valent residue of a compound represented by formula (2-1-1), (2-1-2), or (2-1-3):

wherein:each of R¹ to R⁴ independently represents a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 50 carbon atoms, a substituted or unsubstituted alkoxycarbonyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 50 ring carbon atoms, a substituted or unsubstituted arylthio group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms, a substituted or unsubstituted alkylsilyl group having 1 to 50 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 50 ring carbon atoms, an amino group substituted by a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted haloalkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkenyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkynyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkylamino group having 1 to 50 carbon atoms, a substituted or unsubstituted arylamino group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heteroarylamino group having 5 to 30 ring atoms, a substituted or unsubstituted acylamino group having 2 to 50 carbon atoms, a substituted or unsubstituted heteroaryloxy group having 5 to 30 ring atoms, a substituted or unsubstituted acyl group having 2 to 50 carbon atoms, a substituted or unsubstituted aryloxycarbonyl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted alkylcarbonyl group having 1 to 50 carbon atoms, mercapto group, a substituted or unsubstituted alkylthio group having 1 to 50 carbon atoms, a substituted or unsubstituted arylthio group having 6 to 30 ring carbon atoms, a sulfonyl group, an boryl group, a phosphino group, an amino group, a halogen atom, a cyano group, a nitro group, a hydroxyl group, a carboxyl group, or a valence bonded to L11; andY represents the ring Y.

Further, A11 preferably represents a p-valent residue of a compound represented by formula (2-1-2-1):

wherein:each of X¹ to X⁴ independently represents CR5 or N;each of R¹, R⁴, and R⁵ independently represents a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 50 carbon atoms, a substituted or unsubstituted alkoxycarbonyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms, a substituted or unsubstituted alkylsilyl group having 1 to 50 carbon atoms, a substituted or unsubstituted arylsilyl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted haloalkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkenyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkynyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkylamino group having 1 to 50 carbon atoms, a substituted or unsubstituted arylamino group having 6 to 30 ring carbon atoms, a substituted or unsubstituted heteroarylamino group having 5 to 30 ring atoms, a substituted or unsubstituted acylamino group having 2 to 50 carbon atoms, a substituted or unsubstituted heteroaryloxy group having 5 to 30 ring atoms, a substituted or unsubstituted acyl group having 2 to 50 carbon atoms, a substituted or unsubstituted aryloxycarbonyl group having 6 to 30 ring carbon atoms, a substituted or unsubstituted alkylcarbonyl group having 1 to 50 carbon atoms, a mercapto group, a substituted or unsubstituted alkylthio group having 1 to 50 carbon atoms, a substituted or unsubstituted arylthio group having 6 to 30 ring carbon atoms, a sulfonyl group, an boryl group, a phosphino group, an amino group, a halogen atom, a cyano group, a nitro group, a hydroxyl group, a carboxyl group, or a valence bonded to L11; or R¹, R⁴, and R⁵ are each bonded to each other to form a ring which forms a part of the ring Y.

In particular, the electron transporting layer of the OLED according to the present invention, between the light emitting layer and the cathode, preferably comprises at least one compound of the general formula (I) or (11).

In a preferred embodiment, the electron transporting layer comprising at least one compound of the general formula (I) or (11) further comprises a reducing dopant.

Examples of the reducing dopant include a donating metal, a donating metal compound, and a donating metal complex. The reducing dopant may be used alone or in combination of two or more.

The reducing dopant referred to herein is an electron-donating material. The electron-donating material is a material which generates radical anions by the interaction with a coexisting organic material in the electron transporting layer or an organic material in a layer adjacent to the electron transporting layer, or a material having an electron-donating radical.

The donating metal is a metal having a work function of 3.8 eV or less, preferably an alkali metal, an alkaline earth metal, or a rare earth metal, and more preferably Cs, Li, Na, Sr, K, Mg, Ca, Ba, Yb, Eu, or Ce.

The donating metal compound is a compound comprising the above donating metal, preferably a compound comprising an alkali metal, an alkaline earth metal, or a rare earth metal, and more preferably a halide, an oxide, a carbonate, or a borate of these metals, for example, a compound represented by MO_x (M: donating metal, x: 0.5 to 1.5), MF_x (x: 1 to 3), or M(CO₃)_x (x: 0.5 to 1.5).

The donating metal complex is a complex comprising the above donating metal, preferably an organic metal complex of an alkali metal, an alkaline earth metal or a rare earth metal, and more preferably an organic metal complex represented by formula (I):

MQ_n  (I)

wherein M is a donating metal, Q is a ligand, preferably a carboxylic acid derivative, a diketone derivative, or a quinoline derivative, and n is an integer of 1 to 4.

Examples of the donating metal complex include watermill-shaped tungsten compounds described in JP 2005-72012A and phthalocyanine compounds having an alkali metal or an alkaline earth metal as the central metal, which are described in JP 11-345687A.

The reducing dopant is preferably at least one selected from the group consisting of an alkali metal, an alkaline earth metal, a rare earth metal, an alkali metal oxide, an alkali metal halide, an alkaline earth metal oxide, an alkaline earth metal halide, a rare earth metal oxide, a rare earth metal halide, an organic complex having an alkali metal, an organic complex having an alkaline earth metal, and an organic complex having a rare earth metal, and more preferably a 8-quinolinol complex of an alkali metal.

Examples of the alkali metal includes:

Li (lithium, work function: 2.93 eV),Na (sodium, work function: 2.36 eV),K (potassium, work function: 2.3 eV),Rb (rubidium, work function: 2.16 eV), andCs (cesium, work function: 1.95 eV).

The values of work functions are based on Handbook of Chemistry (Pure Chemistry II, 1984, p. 493, edited by The Chemical Society of Japan). The same applies hereafter.

Preferred examples of the alkaline earth metals are:

Ca (calcium, work function: 2.9 eV),Mg (magnesium, work function: 3.66 eV),Ba (barium, work function: 2.52 eV), andSr (strontium, work function: 2.0 to 2.5 eV).

The work function of strontium is based of Physics of Semiconductor Device (N.Y., Wiley, 1969, p. 366).

Preferred examples of the rare earth metal are:

Yb (ytterbium, work function: 2.6 eV),Eu (europium, work function: 2.5 eV),Gd (gadolinium, work function: 3.1 eV), andEr (erbium, work function: 2.5 eV).

Examples of the alkali metal oxide include Li₂O, LiO, and NaO. The alkaline earth metal oxide is preferably CaO, BaO, SrO, BeO, or MgO.

Examples of the alkali metal halide include a fluoride, for example, LiF, NaF, CsF, and KF and a chloride, for example, LiCl, KCl, and NaCl.

The alkaline earth metal halide is preferably a fluoride, such as CaF₂, BaF₂, SrF₂, MgF₂, and BeF₂ and a halide other than fluoride.

An OLED wherein at least one compound according to general formula (I) or (11) is used in the electron transporting layer is particularly preferred because the driving voltage is reduced while increasing the efficiency.

The content of the at least one compound according to general formula (I) or (11) in the electron transporting layer is preferably 50% by mass or more and more preferably 60% by mass or more.

The electron transport layer facilitates the injection of electrons into the light emitting layer and transports the electrons to the light emitting zone, and has a large electron mobility and an electron affinity generally as large as 2.5 eV or more. The electron transporting layer is preferably formed from a material capable of transporting electrons to the light emitting layer at a lower strength of electric field, preferably having an electron mobility of, for example, at least 10⁻⁶ cm²/V·s under an electric field of 10⁴ to 10⁶ V/cm.

When at least one compound according to general formula (I) or (11) is used in the electron transporting layer, the electron transporting layer may be formed from the at least one compound according to general formula (I) or (11) alone or in combination with another material.

The material for forming the electron injecting/transporting layer in combination with the at least one compound according to general formula (I) or (11) is not particularly limited as long as having the preferred properties mentioned above and may be selected from those commonly used as the electron transporting material in the field of photoconductive materials and those known as the materials for the electron injecting/transporting layer of organic EL devices.

In the present invention, an electron injecting layer including an insulating material or a semiconductor may be disposed between the cathode and the organic layer. By such an electron injecting layer, the leak of electric current is effectively prevented to improve the electron injecting ability. Preferred examples of the insulating material include at least one metal compound selected from the group consisting of an alkali metal chalcogenide, an alkaline earth metal chalcogenide, an alkali metal halide, and an alkaline earth metal halide. An electron injecting layer including the above alkali metal chalcogenide is preferred because the electron injecting property is further improved. Preferred alkali metal chalcogenides include Li₂O, K₂O, Na₂S, Na₂Se, and Na₂O; preferred alkaline earth metal chalcogenides include CaO, BaO, SrO, BeO, BaS, and CaSe; preferred alkali metal halides include LiF, NaF, KF, LiCl, KCl, and NaCl; and preferred alkaline earth metal halides include fluoride such as CaF₂, BaF₂, SrF₂, MgF₂, and BeF₂ and halides other than fluoride.

Examples of the semiconductor for the electron transporting layer include an oxide, a nitride and an oxynitride of at least one element selected from Ba, Ca, Sr, Yb, Al, Ga, In, Li, Na, Cd, Mg, Si, Ta, Sb, and Zn, which are used singly or in combination of two or more. It is preferred that the inorganic compound constituting the electron transporting layer forms a microcrystalline or amorphous insulating thin film. When constituted of the insulating thin film described above, the electron injecting layer is made more uniform to reduce the pixel defect such as dark spots. Examples of such a inorganic compound include the alkali metal chalcogenide, the alkaline earth metal chalcogenide, the alkali metal halide and the alkaline earth metal halide which are described above.

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 Å (angstrom), preferably 1000 to 2000 Å;hole injection layer (b): 50 to 1000 Å, preferably 200 to 800 Å,hole-transport layer (c): 50 to 1000 Å, preferably 100 to 800 Å,exciton blocking layer (d): 10 to 500 Å, preferably 50 to 100 Å,light-emitting layer (e): 10 to 1000 Å, preferably 50 to 600 Å,hole/exciton blocking layer (f): 10 to 500 Å, preferably 50 to 100 Å,electron-transport layer (g): 50 to 1000 Å, preferably 200 to 800 Å,electron injection layer (h): 10 to 500 Å, preferably 20 to 100 Å,cathode (i): 200 to 10 000 Å, preferably 300 to 5000 Å.

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 techniques, 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 according to general formula (I) or (11) in at least one layer of the OLED, preferably in the light-emitting layer, preferably as a host material, a charge transporting material, particularly preferably as a host material and hole or electron transporting material, 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 according to general formula (I) or (11) 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

Synthesis Example 1

Intermediate A-1

10-Bromo-benzo[g]chrysene (3.00 g, 8.40 mmol), which prepared according to the protocol mentioned in a patent application (WO2011086941), 2-chloroaniline (1.07 g, 8.40 mmol), and sodium tert-butoxide (1.61 g, 16.80 mmol) were added to 20 mL of toluene. The reaction mixture was evacuated and purged with argon gas three times. Then, tBu₃P-HBF₄ (244 mg, 0.84 mmol) and Pd₂(dba)₃ (384 mg, 0.42 mmol) were added to the mixture, and the reaction mixture was refluxed overnight. The reaction mixture was cooled to room temperature, and diluted with chloroform. The solid was removed by filtration, and the crude product was chromatographed by eluting with a mixed solvent of heptane and dichloromethane to yield 2.47 g (80%) of A-1 as a beige powder.

LC-MS (m/z): 369 [M+1]

Compound 1

A-1 (600 mg, 1.63 mmol) was combined with 2-(4-bromophenyl)-4-phenylquinazolie (708 mg, 1.96 mmol), which prepared according to the protocol mentioned in a patent application (WO2006049013), Pd₂(dba)₃ (75 mg, 0.082 mmol), ^tBu₃P-HBF₄ (95 mg, 0.326 mmol), and Cs₂CO₃ (1.06 g, 3.26 mmol) in Xylene (16 ml), and then the mixture was degassed under N2 for 5 minutes. The resulting mixture was heated at 130° C. for 48 hours. The reaction mixture was cooled to room temperature and was then filtered through a pad of celite washing out with THF. The filtrate was evaporated to give a crude product. The crude product was purified by flash chromatography with a mixed solvent of heptane and THF as an eluent and was then washed with MeOH to yield 481 mg (46%) of Compound 1 as a yellow solid.

LC-MS (m/z): 648 [M+1]

Synthesis Example 2

Compound 2

A-1 (1.00 g, 2.72 mmol) was combined with 3-(3-bromophenyl)fluoranthene (1.17 g, 3.26 mmol), which prepared according to the protocol mentioned in a patent application (WO2011086935), Pd₂(dba)₃ (0.120 g, 0.136 mmol), ^tBu₃P-HBF₄ (0.158 g, 0.544 mmol), and Cs₂CO₃ (1.77 g, 5.44 mmol) in Xylene (27 ml), and then the mixture was degassed under N2 for 5 minutes. The resulting mixture was heated at 130° C. for 24 hours. The reaction mixture was cooled to room temperature and was then filtered through a pad of celite washing out with THF. The filtrate was evaporated to give a crude product. The crude product was purified by flash chromatography with a mixed solvent of heptane and THF as an eluent and was then washed with MeOH to yield 1.60 g (90%) of Compound 2 as a yellow solid.

LC-MS (m/z): 644 [M+1].

Synthesis Example 3

Compound 3

A-1 (0.95 g, 2.59 mmol), 8-chlorofluoranthene (0.61 g, 2.59 mmol), and sodium tert-butoxide (538 mg, 5.60 mmol) were added to 27 mL of toluene. The reaction mixture was evacuated and purged with argon gas three times. Then, di-t-butyl(2,2-diphenyl-1-methyl-1-cyclopropyl)phosphine (73 mg, 0.21 mmol) and Pd₂(dba)₃ (47 mg, 0.05 mmol) were added to the mixture, and the reaction mixture was stirred at 110° C. overnight. The reaction mixture was cooled to room temperature. Then a solid was collected by filtration, and washed with toluene, water, and ethanol. The crude product was recrystallized with chloroform and ethanol to yield 1.16 g (79%) of Compound 3 as a yellow powder.

LC-MS (m/z): 587

Synthesis Example 4

Intermediate B-1

2-Amino-6-fluorobenzoic acid (35 g, 225.6 mmol) was dissolved in 885 ml of water and 26 mL of acetic acid. The mixture was stirred at 35° C. for 15 min. After that, sodium cyanate (36.67 g, 564 mmol) dissolved in 442 mL of water was added dropwise to the suspension, and the mixture was stirred at 35° C. for 30 min. Then, sodium hydroxide (180.49 g/4.51 mol) was slowly added to the reaction mixture, the mixture was cooled at room temperature. After 374 mL of hydrogen chloride was added there, the precipitate was collected by filtration and washed with water. The solid was dried in a vacuum oven to yield 37.19 (91.5%) of B-1 as white solid. LC-MS (m/z): 180

Intermediate B-2

B-1 (2.6 g, 14.43 mmol) was suspended in 29 mL of toluene and heated to 50° C. Phosphoryl chloride (9.88 mL, 108.25 mmol) was added dropwise, and then DBU (4.31 mL, 28.87 mmol) was added dropwise. The mixture was stirred vigorously at 120° C. for overnight. After the reaction mixture was cooled at room temperature, it was added dropwise to ice-water. The aqueous layer was extracted with ethyl acetate. After it was washed with brine and dried with Na₂SO₄, it was concentrated to give a solid. The crude product was purified by column chromatography on silica gel eluting with toluene to yield 3.41 g (80.8%) of B-2 as a white powder.

It was used for next reaction without purification.

Intermediate B-3

B-2 (2.17 g, 10.0 mmol) and 2-hydroxybenzene boronic acid (1.38 g, 10.0 mmol) were dissolved in 10 mL of THF. To the solution was added potassium fluoride (1.74 g, 30.0 mmol) dissolved in 5 mL of water, and the mixture was evacuated and purged with Argon gas. Then, tBu₃P-HBF₄ (290 mg, 1.00 mmol) and Pd(OAc)₂ (225 mg, 1.00 mmol) were added to the mixture, and the mixture was stirred at room temperature for 1.5 h. The reaction mixture was dried with MgSO₄, filtrated over Celite and washed with ethyl acetate. The crude was purified by column chromatography on silica gel eluting with a mixed solvent of heptane and ethyl acetate (3:1) to yield 2.27 g (96%) of B-3 as a slightly yellow solid.

It was used for next reaction without purification.

Intermediate B-4

B-3 (3.02 g, 11 mmol) was dissolved in 55 mL of DMF and potassium carbonate (1.67 g, 12.1 mmol) was added. The mixture was stirred at room temperature for 5 min. The reaction mixture was diluted with 100 mL of water, and the solid was collected by filtration and washed with water. It was dried in vacuum oven to yield 2.60 g of B-4 as a yellow powder.

LC-MS (m/z): 255, 257

Compound 4

A-1 (1.47 g, 4.00 mmol), B-4 (1.22 g, 4.80 mmol), and sodium tert-butoxide (538 mg, 5.60 mmol) were added to 27 mL of toluene. The reaction mixture was evacuated and purged with argon gas three times. Then, 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene (93 mg, 0.16 mmol) and Pd₂(dba)₃ (73 mg, 0.07 mmol) were added to the mixture, and the reaction mixture was stirred at 80° C. overnight. The reaction mixture was cooled to room temperature. Then a solid was collected by filtration, and washed with toluene, water, and ethanol. The crude product was recrystallized with chloroform and ethanol to yield 2.33 g (99%) of Compound 4 as a yellow powder.

LC-MS (m/z): 586 [M+1]

APPLICATION EXAMPLES

Application Example 1

A glass substrate with 120 nm-thick indium-tin-oxide (ITO) transparent electrode (manufactured by Geomatec Co., Ltd.) used as an anode was first cleaned with isopropanol in an ultrasonic bath for 10 min. To eliminate any possible organic residues, the substrate was exposed to an ultraviolet light and ozone for further 30 min. This treatment also improved the hole injection properties of the ITO. The cleaned substrate was mounted on a substrate holder and loaded into a vacuum chamber.

Thereafter, the organic materials specified below were applied by vapor deposition to the ITO substrate at a rate of approx. 0.2-1 Å/sec at about 10⁻⁶-10⁻⁸ mbar. As the first layer, 5 nm-thick of electron accepting compound A was vapor-deposited. Then 220 nm-thick of aromatic amine compound B was applied as a hole transporting layer. Then, a mixture of 2% by weight of an emitter compound (Compound D), 98% by weight of a host (compound 1) were applied to form a 40 nm-thick phosphorescent-emitting layer. On the emitting layer, 50% by weight of an electron transporting compound, Compound C, 50% by weight of Liq (8-Hydroxyquinolate lithium) was applied to form 25 nm-thick electron transport layer. Finally, 1 nm-thick LiF was deposited as an electron injection layer and 80 nm-thick Al was then deposited as a cathode to complete the device. The device was sealed with a glass lid and a getter in an inert nitrogen atmosphere with less than 1 ppm of water and oxygen.

Application Examples 2 and 3

Application Example 1 were repeated except that the host (Compound 1) is replaced by Compound 2 (Application Example 2) and Comparative 1 (Application Example 3).

OLED Characterization

To characterize the OLED, electroluminescence spectra were recorded at various currents and voltages. In addition, the current-voltage characteristic was measured in combination with the luminance to determine external quantum efficiency (EQE). Driving voltage U and EQE were given at 10 mA/cm². The results are shown in Table 1.

	TABLE 1
	Appl. Ex.	Host	U (V)	EQE (%)
	Appl. Ex. 1	Compound 1	4.91	14.03
	Appl. Ex. 2	Compound 2	4.80	14.27
	Appl. Ex. 3	Comparative 1	5.12	13.08

The results of Table 1 demonstrate that the compounds 1 and 2 can be used as a phosphorescent hosts, and they show lower driving voltage and higher efficiency than Comparative 1.

Claims

1. A compound of formula (11):

2. The compound according to claim 1, wherein R100 is an aryl group having 6 to 30 carbon atoms which is unsubstituted or substituted by at least one group G or a heteroaryl group having 5 to 30 ring atoms which is unsubstituted or substituted by at least one group G.

3. The compound according to claim 1, wherein the aryl group for R100 is a phenyl group or a fused aryl group having 10 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G.

4. The compound according to claim 3, wherein the fused aryl group is selected from the group consisting of a naphthyl group, a fluoranthenyl group, a triphenylenyl group, a benzotriphenylenyl group, a phenanthryl group, and a fluorenyl group.

5. The compound according to claim 1, wherein the heteroaryl group for R100 is selected from the group consisting of a heteroaryl group comprising a nitrogen-comprising six membered ring, a dibenzofuranyl group, a dibenzothiophenyl group, and a carbazolyl group, to each of which at least one selected from the group consisting of a six membered, aromatic hydrocarbon ring, a five or six membered, non-aromatic hydrocarbon ring, a five or six membered, aromatic heterocyclic ring, and a five or six membered, non-aromatic heterocyclic ring is optionally fused.

6. The compound according to claim 5, wherein the heteroaryl group comprising a nitrogen-comprising six membered ring is of formula (12):

7. The compound according to claim 6, wherein the heteroaryl group of the formula (12) corresponds to a pyridinyl group, a pyrimidinyl group or a triazinyl group, each of which is unsubstituted or substituted by at least one group G.

8. The compound according to claim 6, wherein the heteroaryl group of the formula (12) corresponds to formula (15):

9. The compound according to claim 6, wherein the heteroaryl group of the formula (12) corresponds to formula (16) or (17):

10. The compound according to claim 6, wherein the heteroaryl group of the formulae (12) corresponds to any of formulae (18) to (23):

11. The compound according to claim 6, wherein the heteroaryl group of the formula (12) corresponds to formula (24):

12. The compound according to claim 11, wherein the heteroaryl group of the formula (24) corresponds to formula (25):

13. The compound according to claim 12, wherein the heteroaryl group of the formula (25) corresponds to any of formulae (26) to (29):

14. The compound according to claim 12, wherein the heteroaryl group of the formula (25) corresponds to any of formulae (30) to (33):

15. The compound according to claim 1, wherein n100 is 1 andL100 is an arylene group having 6 to 30 ring carbon atoms which is unsubstituted or substituted by at least one group G.

16. The compound according to claim 1, wherein n100 is 1 andL100 is a direct bond.

17. The compound according to claim 1, wherein R101 to R116 are all hydrogen atoms.

18. A material for an organic electroluminescence device comprising the compound of claim 1.

19. An organic electroluminescence device, comprising the compound of claim 1.

20. The organic electroluminescence device according to claim 19, comprising: a cathode,an anode, anda plurality of organic layers provided between the cathode and the anode,wherein at least one of the plurality of the organic layers comprises the compound.

21. The organic electroluminescence device according to claim 20, wherein the organic layers comprise an emitting layer comprising the compound as a host material.

22. The organic electroluminescence device according to claim 21, wherein the host material is a phosphorescent host material.

23. The organic electroluminescence device according to claim 20, wherein the organic layers comprise an electron transporting layer comprising the compound.

24. The organic electroluminescence device according to claim 23, wherein the electron transporting layer comprises:at least one selected from the group consisting of an alkali metal, an alkaline earth metal, a rare earth metal, a compound comprising an alkali metal, an alkaline earth metal, and a rare earth metal, anda complex comprising an alkali metal, an alkaline earth metal, or a rare earth metal.

25. (canceled)