WO2019238471A1

WO2019238471A1 - Organic molecules for optoelectronic devices

Info

Publication number: WO2019238471A1
Application number: PCT/EP2019/064498
Authority: WO
Inventors: Sebastian DÜCK; Anna RUF; Damien JOLY
Original assignee: Cynora GmbH
Current assignee: Cynora GmbH
Priority date: 2018-06-14
Filing date: 2019-06-04
Publication date: 2019-12-19
Anticipated expiration: 2020-12-14
Also published as: DE102018114290B3; CN112334447A

Abstract

The invention relates to an organic molecule for the use in optoelectronic devices. According to the invention, the organic compound has - a first chemical moiety with a structure of formula (I) and - three second chemical moieties, each independently from another with a structure of formula (II), wherein the first chemical moiety is linked to each of the three second chemical moieties via a single bond; T, V, X, Y is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R1; W is CN; Rv, Rw, RY is Rl; Rx is CN; RT is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties; wherein exactly two substituents selected from the group consisting of T, V, X and Y represent the binding site of a single bond linking the first chemical moiety and one of the three second chemical moieties.

Description

ORGANIC MOLECULES

FOR OPTOELECTRONIC DEVICES

The invention relates to organic molecules and their use in organic light-emitting diodes (OLEDs) and in other optoelectronic devices.

Description

An object of the present invention is to provide molecules which are suitable for use in optoelectronic devices.

This object is achieved by the invention which provides a new class of organic molecules.

The organic molecules of the invention are preferably purely organic molecules, i.e. they do not contain any metal ions, which is in contrast to metal complexes known for use in optoelectronic devices. Therefore, according to the present invention, it is preferred that the organic molecules are free of metal atoms or metal ions. The pure organic molecules may, however, in concordance with modern era definitions include metalloids, in particular, B and Si or exceptionally Sn, Se and Ge.

According to the present invention, the organic molecules exhibit emission maxima in the blue, sky-blue or green spectral range. The organic molecules exhibit, in particular, emission maxima between 420 nm and 520 nm, between 440 nm and 495 nm, or between 450 nm and 470 nm. The photoluminescence quantum yields of the organic molecules according to the invention are, in particular, 20 % or more. The molecules according to the invention show, in particular, thermally activated delayed fluorescence (TADF). The use of the molecules according to the invention in an optoelectronic device, for example, in an organic light-emitting diode (OLED), leads to higher efficiencies of the device. Corresponding OLEDs have a higher stability than OLEDs with known emitter materials and comparable color.

The organic light-emitting molecules of the invention comprise or consist of a first chemical moiety comprising or consisting of a structure of formula I,

Formula I and

- three second chemical moieties, each independently from another comprising or consisting of a structure of formula II,

Formula II wherein the first chemical moiety is linked to each of the three second chemical moieties via a single bond.

T is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹.

V is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹.

W is CN.

X is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹.

Y is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹.

R^T is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties.

R^v is R'.

R^w is R'.

R^x is CN.

R^Y is R'. # represents the binding site of a single bond linking the second chemical moieties to the first chemical moiety;

Z is at each occurrence independently from another selected from the group consisting of a direct bond, CR³R⁴, C=CR³R⁴, C=0, C=NR³, NR³, O, SiR³R⁴, S, S(O) and S(0)₂;

R¹ is at each occurrence independently from another selected from the group consisting of: hydrogen,

deuterium,

Ci-C₅-alkyl,

wherein one or more hydrogen atoms are optionally substituted by deuterium;

C₂-C₈-alkenyl,

wherein one or more hydrogen atoms are optionally substituted by deuterium;

C₂-C₈-alkynyl,

wherein one or more hydrogen atoms are optionally substituted by deuterium; and Ce-Cis-aryl,

which is optionally substituted with one or more substituents R⁶.

R' is at each occurrence independently from another selected from the group consisting of: hydrogen,

deuterium,

Ci-C₅-alkyl,

wherein one or more hydrogen atoms are optionally substituted by deuterium;

C₂-Cs-alkenyl,

wherein one or more hydrogen atoms are optionally substituted by deuterium;

C₂-Cs-alkynyl,

which is optionally substituted with one or more substituents R⁶.

R^a, R³ and R⁴ is at each occurrence independently from another selected from the group consisting of hydrogen, deuterium, N(R⁵)₂, OR⁵, Si(R⁵)₃, B(OR⁵)₂, OSO₂R⁵, CF₃, CN, F, Br, I, Ci-C₄o-alkyl,

which is optionally substituted with one or more substituents R⁵ and

wherein one or more non-adjacent CFh-groups are optionally substituted by R⁵C=CR⁵, CºC, Si(R⁵)₂, Ge(R⁵)₂, Sn(R⁵)₂, C=0, C=S, C=Se, C=NR⁵, P(=0)(R⁵), SO, S0₂, NR⁵, O, S or CONR⁵;

Ci-C₄o-alkoxy, which is optionally substituted with one or more substituents R⁵ and

wherein one or more non-adjacent CH₂-groups are optionally substituted by R⁵C=CR⁵, CºC, Si(R⁵)₂, Ge(R⁵)₂, Sn(R⁵)₂, C=0, C=S, C=Se, C=NR⁵, P(=0)(R⁵), SO, S0₂, NR⁵, O, S or CONR⁵;

Ci-C₄o-thioalkoxy,

which is optionally substituted with one or more substituents R⁵ and

C₂-C₄o-alkenyl,

which is optionally substituted with one or more substituents R⁵ and

C₂-C₄o-alkynyl,

which is optionally substituted with one or more substituents R⁵ and

Ce-Ceo-aryl,

which is optionally substituted with one or more substituents R⁵; and

C3-C57-heteroaryl,

which is optionally substituted with one or more substituents R⁵.

R⁵ is at each occurrence independently from another selected from the group consisting of: hydrogen, deuterium, N(R⁶)₂, OR⁶, Si(R⁶)₃, B(OR⁶)₂, 0S0₂R⁶, CF₃, CN, F, Br, I,

Ci-C₄o-alkyl,

which is optionally substituted with one or more substituents R⁶ and

wherein one or more non-adjacent CH₂-groups are optionally substituted by R⁶C=CR⁶, CºC, Si(R⁶)₂, Ge(R⁶)₂, Sn(R⁶)₂, C=0, C=S, C=Se, C=NR⁶, P(=0)(R⁶), SO, S0₂, NR⁶, O, S or CONR⁶;

Ci-C₄o-alkoxy,

which is optionally substituted with one or more substituents R⁶ and

Ci-C₄o-thioalkoxy,

which is optionally substituted with one or more substituents R⁶ and wherein one or more non-adjacent CFh-groups are optionally substituted by R⁶C=CR⁶, CºC, Si(R⁶)₂, Ge(R⁶)₂, Sn(R⁶)₂, C=0, C=S, C=Se, C=NR⁶, P(=0)(R⁶), SO, S0₂, NR⁶, O, S or CONR⁶;

C2-C₄o-alkenyl,

which is optionally substituted with one or more substituents R⁶ and

wherein one or more non-adjacent CFh-groups are optionally substituted by R⁶C=CR⁶, CºC, Si(R⁶)₂, Ge(R⁶)₂, Sn(R⁶)₂, C=0, C=S, C=Se, C=NR⁶, P(=0)(R⁶), SO, S0₂, NR⁶, O, S or CONR⁶;

C2-C₄o-alkynyl,

which is optionally substituted with one or more substituents R⁶ and

Ce-Ceo-aryl,

which is optionally substituted with one or more substituents R⁶; and

C3-C57-heteroaryl,

which is optionally substituted with one or more substituents R⁶.

R⁶ is at each occurrence independently from another selected from the group consisting of: hydrogen, deuterium, OPh (Ph = phenyl), CF3, CN, F,

Ci-C5-alkyl,

wherein optionally one or more hydrogen atoms are independently from each other substituted by deuterium, CN, CF3, or F;

Ci-Cs-alkoxy,

Ci-Cs-thioalkoxy,

C2-C5-alkenyl,

C2-C5-alkynyl,

Ce-Cis-aryl,

which is optionally substituted with one or more C-i-Cs-alkyl substituents; C₃-Ci₇-heteroaryl,

which is optionally substituted with one or more C-i-Cs-alkyl substituents;

N(C6-Ci8-aryl)2,

N(C3-Ci7-heteroaryl)2; and

N(C₃-Ci₇-heteroaryl)(C₆-Ci₈-aryl).

The substituents R^a, R³, R⁴ or R⁵ independently from each other can optionally form a mono- or polycyclic, aliphatic, aromatic and/or benzo-fused ring system with one or more substituents R^a, R³, R⁴ or R⁵.

According to the invention exactly two substituents selected from the group consisting of T, V, X and Y represent the binding site of a single bond linking the first chemical moiety and one of the three second chemical moieties.

In one embodiment of the invention, first chemical moiety comprises or consists of a structure of formula la:

Formula la wherein R' and R¹ are defined as above,

T^m is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹,

\J^m is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹,

X^m is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹,

R^T is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties, wherein exactly two substituent selected from the group consisting of X", V^m and ^M represent the binding site of a single bond linking the first chemical moiety and one of the three second chemical moieties.

In one embodiment of the invention, first chemical moiety comprises or consists of a structure of formula laa:

Formula laa

wherein R¹ and R¹ are defined as above,

T^# is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties,

V^# is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties,

In one embodiment of the invention, first chemical moiety comprises or consists of a structure of formula laaa:

Formula laaa wherein R' and R¹ are defined as above, X^# is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties,

In one embodiment, R¹ and R' is at each occurrence independently from another selected from the group consisting of hydrogen (H), methyl, mesityl, tolyl and phenyl (Ph). The term tolyl refers to 2-tolyl, 3-tolyl, and 4-tolyl.

In one embodiment, R¹ and R' is at each occurrence independently from another selected from the group consisting of hydrogen (H) and phenyl.

In one embodiment, R¹ and R' is at each occurrence hydrogen (H).

In one embodiment, T, V and R^T is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties.

In one embodiment, V, X and R^T is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties.

In a further embodiment of the invention, each of the three second chemical moieties at each occurrence independently from another comprise or consist of a structure of formula I la:

Formula lla wherein # and R^a are defined as above.

In a further embodiment of the invention, R^a is at each occurrence independently from another selected from the group consisting of: H,

Me,

iPr, ^lBu,

CN,

CFs,

Ph, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph,

pyridinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph,

pyrimidinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph, carbazolyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph, triazinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph,

and N(Ph)₂.

Me,

'Pr,

lBu,

CN,

CF₃,

pyrimidinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph, and triazinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph.

Me,

lBu,

Ph, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph, triazinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph.

In a further embodiment of the invention, R^a is H at each occurrence.

In a further embodiment of the invention, the three second chemical moieties each at each occurrence independently from another comprise or consist of a structure of formula lib, a structure of formula I lb-2, a structure of formula llb-3 or a structure of formula llb-4:

Formula lib Formula llb-2 Formula llb-3 Formula llb-4 wherein

R^b is at each occurrence independently from another selected from the group consisting of:

H,

deuterium,

N(R⁵)₂,

OR⁵,

Si(R⁵)₃,

B(OR⁵)₂,

OSO₂R⁵,

CFs,

CN,

F,

Br,

I,

Ci-C₄o-alkyl,

which is optionally substituted with one or more substituents R⁵ and

Ci-C₄o-alkoxy,

which is optionally substituted with one or more substituents R⁵ and wherein one or more non-adjacent CH₂-groups are optionally substituted by R⁵C=CR⁵, CºC, Si(R⁵)₂, Ge(R⁵)₂, Sn(R⁵)₂, C=0, C=S, C=Se, C=NR⁵, P(=0)(R⁵), SO, S0₂, NR⁵, O, S or CONR⁵;

Ci-C40-thioalkoxy,

which is optionally substituted with one or more substituents R⁵ and

C₂-C₄o-alkenyl,

which is optionally substituted with one or more substituents R⁵ and

C₂-C₄o-alkynyl,

which is optionally substituted with one or more substituents R⁵ and

Ce-Ceo-aryl,

which is optionally substituted with one or more substituents R⁵; and

C3-C57-heteroaryl,

which is optionally substituted with one or more substituents R⁵.

Apart from that, the aforementioned definitions apply.

In one additional embodiment of the invention, the three second chemical moieties each at each occurrence independently from another comprise or consist of a structure of formula lie, a structure of formula llc-2, a structure of formula llc-3, or a structure of formula llc-4:

Formula lie Formula llc-2 Formula llc-3 Formula llc-4 wherein the aforementioned definitions apply.

In a further embodiment of the invention, R^b is at each occurrence independently from another selected from the group consisting of:

H, Me,

Vr,

lBu,

CN,

CFs,

Ph, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph;

pyridinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph;

carbazolyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph;

triazinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph;

and N(Ph)₂.

H,

Me,

'Pr,

lBu,

CN,

CF₃,

pyrimidinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph; and triazinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph.

H,

Me,

lBu, Ph, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph;

triazinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph.

In the following, examples of the second chemical moiety are shown:

wherein for #, Z, R^a, R³, R⁴ and R⁵, the aforementioned definitions apply.

In one embodiment, R^a and R⁵ is at each occurrence independently from another selected from the group consisting of hydrogen (H), methyl (Me), i-propyl (CH(CH₃)₂) ('Pr), t-butyl fBu), phenyl (Ph), CN, CF₃, and diphenylamine (NPfi₂).

In a further embodiment of the invention, the three second chemical moieties are identical at each occurrence.

In a further embodiment of the invention, at least two of the three second chemical moieties are identical.

In one embodiment of the invention, the organic molecules comprise or consist of a structure of formula III:

wherein the aforementioned definitions apply.

In a further embodiment of the invention, the organic molecules comprise or consist of a structure of formula Ilia:

Formula Ilia

wherein

R^c is at each occurrence independently from another selected from the group consisting of: H,

Me,

iPr,

lBu,

Ph, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph; pyridinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph;

pyrimidinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃, and Ph;

and N(Ph)₂.

In a further embodiment of the invention, the organic molecules comprise or consist of a structure formula lllb:

Formula lllb

wherein the aforementioned definitions apply.

In one embodiment of the invention, the organic molecules comprise or consist of a structure of formula IV:

Formula IV

wherein the aforementioned definitions apply.

In a further embodiment of the invention, the organic molecules comprise or consist of a structure of formula IVa

Formula IVa

wherein the aforementioned definitions apply.

In a further embodiment of the invention, the organic molecules comprise or consist of a structure selected from the group of formula IVb:

Formula IVb

wherein the aforementioned definitions apply.

In one embodiment of the invention, R^c is at each occurrence independently from another selected from the group consisting of:

H,

Me,

iPr,

lBu,

Ph, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃ and Ph; and

triazinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃ and Ph.

As used throughout the present application, the terms "aryl" and "aromatic" may be understood in the broadest sense as any mono-, bi- or polycyclic aromatic moieties. Accordingly, an aryl group contains 6 to 60 aromatic ring atoms, and a heteroaryl group contains 5 to 60 aromatic ring atoms, of which at least one is a heteroatom. Notwithstanding, throughout the application the number of aromatic ring atoms may be given as subscripted number in the definition of certain substituents. In particular, the heteroaromatic ring includes one to three heteroatoms. Again, the terms“heteroaryl" and“heteroaromatic” may be understood in the broadest sense as any mono-, bi- or polycyclic hetero-aromatic moieties that include at least one heteroatom. The heteroatoms may at each occurrence be the same or different and be individually selected from the group consisting of N, O and S. Accordingly, the term "arylene" refers to a divalent substituent that bears two binding sites to other molecular structures and thereby serving as a linker structure. In case, a group in the exemplary embodiments is defined differently from the definitions given here, for example, the number of aromatic ring atoms or number of heteroatoms differs from the given definition, the definition in the exemplary embodiments is to be applied. According to the invention, a condensed (annulated) aromatic or heteroaromatic polycycle is built of two or more single aromatic or heteroaromatic cycles, which formed the polycycle via a condensation reaction.

In particular, as used throughout the present application, the term“aryl group” or“heteroaryl group” comprises groups which can be bound via any position of the aromatic or heteroaromatic group, derived from benzene, naphthaline, anthracene, phenanthrene, pyrene, dihydropyrene, chrysene, perylene, fluoranthene, benzanthracene, benzphenanthrene, tetracene, pentacene, benzpyrene, furan, benzofuran, isobenzofuran, dibenzofuran, thiophene, benzothiophene, isobenzothiophene, dibenzothiophene; pyrrole, indole, isoindole, carbazole, pyridine, quinoline, isoquinoline, acridine, phenanthridine, benzo-5, 6-quinoline, benzo-6, 7-quinoline, benzo-7, 8-quinoline, phenothiazine, phenoxazine, pyrazole, indazole, imidazole, benzimidazole, naphthoimidazole, phenanthroimidazole, pyridoimidazole, pyrazinoimidazole, quinoxalinoimidazole, oxazole, benzoxazole, napthooxazole, anthroxazol, phenanthroxazol, isoxazole, 1 ,2-thiazole, 1 ,3-thiazole, benzothiazole, pyridazine, benzopyridazine, pyrimidine, benzopyrimidine, 1 ,3,5-triazine, quinoxaline, pyrazine, phenazine, naphthyridine, carboline, benzocarboline, phenanthroline, 1 ,2,3-triazole, 1 ,2,4- triazole, benzotriazole, 1 ,2,3-oxadiazole, 1 ,2,4-oxadiazole, 1 ,2,5-oxadiazole, 1 ,2,3,4-tetrazine, purine, pteridine, indolizine and benzothiadiazole or combinations of the abovementioned groups.

As used throughout the present application, the term“cyclic group” may be understood in the broadest sense as any mono-, bi- or polycyclic moieties.

As used throughout the present application, the term biphenyl as a substituent may be understood in the broadest sense as ortho-biphenyl, meta-biphenyl, or para-biphenyl, wherein ortho, meta and para is defined in regard to the binding site to another chemical moiety.

As used throughout the present application, the term“alkyl group” may be understood in the broadest sense as any linear, branched, or cyclic alkyl substituent. In particular, the term alkyl comprises the substituents methyl (Me), ethyl (Et), n-propyl (ⁿPr), i-propyl ('Pr), cyclopropyl, n- butyl (ⁿBu), i-butyl ('Bu), s-butyl (^sBu), t-butyl fBu), cyclobutyl, 2-methylbutyl, n-pentyl, s-pentyl, t-pentyl, 2-pentyl, neo-pentyl, cyclopentyl, n-hexyl, s-hexyl, t-hexyl, 2-hexyl, 3-hexyl, neo-hexyl, cyclohexyl, 1 -methylcyclopentyl, 2-methylpentyl, n-heptyl, 2-heptyl, 3-heptyl, 4-heptyl, cycloheptyl, 1 -methylcyclohexyl, n-octyl, 2-ethylhexyl, cyclooctyl, 1 -bicyclo[2,2,2]octyl, 2- bicyclo[2,2,2]-octyl, 2-(2,6-dimethyl)octyl, 3-(3,7-dimethyl)octyl, adamantyl, 2,2,2-trifluorethyl, 1 , 1 -dimethyl-n-hex-1 -yl, 1 ,1 -dimethyl-n-hept-1 -yl, 1 ,1 -dimethyl-n-oct-1 -yl, 1 ,1 -dimethyl-n-dec- 1 -yl, 1 ,1 -dimethyl-n-dodec-1 -yl, 1 ,1 -dimethyl-n-tetradec-1 -yl, 1 ,1 -dimethyl-n-hexadec-1 -yl, 1 , 1 -dimethyl-n-octadec-1 -yl, 1 ,1 -diethyl-n-hex-1 -yl, 1 ,1 -diethyl-n-hept-1 -yl, 1 ,1 -diethyl-n-oct-1 - yl, 1 , 1 -diethyl-n-dec-1 -yl, 1 , 1 -diethyl-n-dodec-1 -yl, 1 , 1 -d iethyl-n-tetradec-1 -yl , 1 ,1 -diethyln-n- hexadec-1 -yl, 1 ,1 -diethyl-n-octadec-1 -yl, 1 -(n-propyl)-cyclohex-l -yl, 1 -(n-butyl)-cyclohex-l -yl, 1 -(n-hexyl)-cyclohex-1 -yl, 1 -(n-octyl)-cyclohex-1 -yl and 1 -(n-decyl)-cyclohex-1 -yl.

As used throughout the present application, the term“alkenyl” comprises linear, branched, and cyclic alkenyl substituents. The term alkenyl group exemplarily comprises the substituents ethenyl, propenyl, butenyl, pentenyl, cyclopentenyl, hexenyl, cyclohexenyl, heptenyl, cycloheptenyl, octenyl, cyclooctenyl or cyclooctadienyl.

As used throughout the present application, the term“alkynyl” comprises linear, branched, and cyclic alkynyl substituents. The term“alkynyl group” exemplarily comprises ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl or octynyl.

As used throughout the present application, the term“alkoxy” comprises linear, branched, and cyclic alkoxy substituents. The term“alkoxy group” exemplarily comprises methoxy, ethoxy, n- propoxy, i-propoxy, n-butoxy, i-butoxy, s-butoxy, t-butoxy and 2-methylbutoxy.

As used throughout the present application, the term“thioalkoxy” comprises linear, branched, and cyclic thioalkoxy substituents, in which the O of the exemplarily alkoxy groups is replaced by S.

As used throughout the present application, the terms“halogen” and“halo” may be understood in the broadest sense as being preferably fluorine, chlorine, bromine or iodine.

Whenever hydrogen (H) is mentioned herein, it could also be replaced by deuterium at each occurrence.

It is understood that when a molecular fragment is described as being a substituent or otherwise attached to another moiety, its name may be written as if it were a fragment (e.g. naphtyl, dibenzofuryl) or as if it were the whole molecule (e.g. naphthalene, dibenzofuran). As used herein, these different ways of designating a substituent or attached fragment are considered to be equivalent. In one embodiment, the organic molecules according to the invention have an excited state lifetime of not more than 150 ps, of not more than 100 ps, in particular of not more than 50 ps, more preferably of not more than 10 ps or not more than 7 ps in a film of poly(methyl methacrylate) (PMMA) with 10 % by weight of organic molecule at room temperature.

In one embodiment of the invention, the organic molecules according to the invention represent thermally-activated delayed fluorescence (TADF) emitters, which exhibit a AEST value, which corresponds to the energy difference between the first excited singlet state (S1 ) and the first excited triplet state (T1 ), of less than 5000 cm ¹, preferably less than 3000 cm ¹, more preferably less than 1500 cm ¹, even more preferably less than 1000 cm ¹ or even less than 500 cm ¹.

In a further embodiment of the invention, the organic molecules according to the invention have an emission peak in the visible or nearest ultraviolet range, i.e., in the range of a wavelength of from 380 to 800 nm, with a full width at half maximum of less than 0.50 eV, preferably less than 0.48 eV, more preferably less than 0.45 eV, even more preferably less than 0.43 eV or even less than 0.40 eV in a film of poly(methyl methacrylate) (PMMA) with 10 % by weight of organic molecule at room temperature.

In a further embodiment of the invention, the organic molecules according to the invention have a“blue material index” (BMI), calculated by dividing the photoluminescence quantum yield (PLQY) in % by the CIEy color coordinate of the emitted light, of more than 150, in particular more than 200, preferably more than 250, more preferably of more than 300 or even more than 500.

In a further embodiment of the invention, the organic molecules according to the invention have a PLQY in % of more than 60%, in particular more than 64%, preferably more than 75%, more preferably of more than 80% or even more than 83%.

In a further embodiment of the invention, the organic molecules according to the invention have a PLQY in % of more than 80% or even more than 83%.

Orbital and excited state energies can be determined either by means of experimental methods or by calculations employing quantum-chemical methods, in particular, density functional theory calculations. The energy of the highest occupied molecular orbital E^HOMO is determined by methods known to the person skilled in the art from cyclic voltammetry measurements with an accuracy of 0.1 eV. The energy of the lowest unoccupied molecular orbital E^LUMO is calculated as E^HOMO + E^gap, wherein E^gap is determined as follows: For host compounds, the onset of the emission spectrum of a film with 10 % by weight of host in poly(methyl methacrylate) (PMMA) is used as E^gap, unless stated otherwise. For emitter molecules, E^gap is determined as the energy at which the excitation and emission spectra of a film with 10 % by weight of emitter in PMMA cross.

The energy of the first excited triplet state T 1 is determined from the onset of the emission spectrum at low temperature, typically at 77 K. For host compounds, where the first excited singlet state and the lowest triplet state are energetically separated by > 0.4 eV, the phosphorescence is usually visible in a steady-state spectrum in 2-Me-THF. The triplet energy can thus be determined as the onset of the phosphorescence spectrum. For TADF emitter molecules, the energy of the first excited triplet state T1 is determined from the onset of the delayed emission spectrum at 77 K, if not otherwise stated measured in a film of PMMA with 10 % by weight of emitter. Both for host and emitter compounds, the energy of the first excited singlet state S1 is determined from the onset of the emission spectrum, if not otherwise stated measured in a film of PMMA with 10 % by weight of host or emitter compound.

The onset of an emission spectrum is determined by computing the intersection of the tangent to the emission spectrum with the x-axis. The tangent to the emission spectrum is set at the high-energy side of the emission band and at the point at half maximum of the maximum intensity of the emission spectrum.

A further aspect of the invention relates to a process for preparing organic molecules (with an optional subsequent reaction) according to the invention, wherein a tri-R'-substituted 3-bromo- 4-fluoro-benzonitrile is used as a reactant:

For the reaction of a nitrogen heterocycle in a nucleophilic aromatic substitution with an aryl halide, preferably an aryl fluoride, typical conditions include the use of a base, such as tribasic potassium phosphate or sodium hydride, for example, in an aprotic polar solvent, such as dimethyl sulfoxide (DMSO) or N,N-dimethylformamide (DMF), for example.

An alternative synthesis route comprises the introduction of a nitrogen heterocycle via copper- or palladium-catalyzed coupling to an aryl halide or aryl pseudohalide, preferably an aryl bromide, an aryl iodide, aryl triflate or an aryl tosylate.

A further aspect of the invention relates to the use of an organic molecule according to the invention as a luminescent emitter or as an absorber, and/or as host material and/or as electron transport material, and/or as hole injection material, and/or as hole blocking material in an optoelectronic device.

The optoelectronic device, also referred to as organic optoelectronic device, may be understood in the broadest sense as any device based on organic materials that is suitable for emitting light in the visible or nearest ultraviolet (UV) range, i.e., in the range of a wavelength of from 380 nm to 800 nm. More preferably, the optoelectronic device may be able to emit light in the visible range, i.e., of from 400 nm to 800 nm.

In the context of such use, the optoelectronic device is more particularly selected from the group consisting of:

• organic light-emitting diodes (OLEDs),

• light-emitting electrochemical cells,

• OLED sensors, especially in gas and vapour sensors not hermetically externally shielded,

• organic diodes,

• organic solar cells,

• organic transistors,

• organic field-effect transistors,

• organic lasers, and

• down-conversion elements.

In a preferred embodiment in the context of such use, the optoelectronic device is a device selected from the group consisting of an organic light emitting diode (OLED), a light emitting electrochemical cell (LEC), and a light-emitting transistor.

In the case of the use, the fraction of the organic molecule according to the invention in the emission layer in an optoelectronic device, more particularly in OLEDs, is 1 % to 99 % by weight, more particularly 5 % to 80 % by weight. In an alternative embodiment, the proportion of the organic molecule in the emission layer is 100 % by weight.

In one embodiment, the light-emitting layer comprises not only the organic molecules according to the invention but also a host material whose triplet (T1 ) and singlet (S1 ) energy levels are energetically higher than the triplet (T 1 ) and singlet (S1 ) energy levels of the organic molecule.

A further aspect of the invention relates to a composition comprising or consisting of:

(a) at least one organic molecule according to the invention, in particular in the form of an emitter and/or a host, and

(b) one or more emitter and/or host materials, which differ from the organic molecule according to the invention, and

(c) optionally, one or more dyes and/or one or more solvents. In one embodiment, the light-emitting layer comprises (or essentially consists of) a composition comprising or consisting of:

(b) one or more emitter and/or host materials, which differ from the organic molecule according to the invention and

(c) optional one or more dyes and/or one or more solvents.

Particularly preferably the light-emitting layer EML comprises (or essentially consists of) a composition comprising or consisting of:

(i) 1 -50 % by weight, preferably 5-40 % by weight, in particular 10-30 % by weight, of one or more organic molecules according to the invention E;

(ii) 5-99 % by weight, preferably 30-94.9 % by weight, in particular 40-89% by weight, of at least one host compound H; and

(iii) optionally 0-94 % by weight, preferably 0.1 -65 % by weight, in particular 1 -50 % by weight, of at least one further host compound D with a structure differing from the structure of the molecules according to the invention; and

(iv) optionally 0-94 % by weight, preferably 0-65 % by weight, in particular 0-50 % by weight, of a solvent; and

(v) optionally, 0-30 % by weight, in particular 0-20 % by weight, preferably 0-5 % by weight, of at least one further emitter molecule F with a structure differing from the structure of the molecules according to the invention.

Preferably, energy can be transferred from the host compound H to the one or more organic molecules according to the invention (E), in particular transferred from the first excited triplet state T1 (H) of the host compound H to the first excited triplet state T1 (E) of the one or more organic molecules according to the invention E and / orfrom the first excited singlet state S1 (H) of the host compound H to the first excited singlet state S1 (E) of the one or more organic molecules according to the invention E.

In a further embodiment, the light-emitting layer EML comprises (or (essentially) consists of) a composition comprising or consisting of:

(i) 1 -50 % by weight, preferably 5-40 % by weight, in particular 10-30 % by weight, of one organic molecule according to the invention E;

(ii) 5-99 % by weight, preferably 30-94.9 % by weight, in particular 40-89% by weight, of one host compound H; and (iii) optionally, 0-94 % by weight, preferably 0.1 -65 % by weight, in particular 1 -50 % by weight, of at least one further host compound D with a structure differing from the structure of the molecules according to the invention; and

(iv) optionally, 0-94 % by weight, preferably 0-65 % by weight, in particular 0-50 % by weight, of a solvent; and

In one embodiment, the host compound H has a highest occupied molecular orbital HOMO(H) having an energy E^HOMO(H) in the range of from -5 to -6.5 eV and the at least one further host compound D has a highest occupied molecular orbital HOMO(D) having an energy E^HOMO(D), wherein E^HOMO(H) > E^HOMO(D).

In a further embodiment, the host compound H has a lowest unoccupied molecular orbital LUMO(H) having an energy E^LUMO(H) and the at least one further host compound D has a lowest unoccupied molecular orbital LUMO(D) having an energy E^LUMO(D), wherein E^LUMO(H)

> _ELUMO )_

In one embodiment, the host compound H has a highest occupied molecular orbital HOMO(H) having an energy E^HOMO(H) and a lowest unoccupied molecular orbital LUMO(H) having an energy E^LUMO(H), and

the at least one further host compound D has a highest occupied molecular orbital HOMO(D) having an energy E^HOMO(D) and a lowest unoccupied molecular orbital LUMO(D) having an energy E^LUMO(D),

the organic molecule according to the invention (E) has a highest occupied molecular orbital HOMO(E) having an energy E^HOMO(E) and a lowest unoccupied molecular orbital LUMO(E) having an energy E^LUMO(E),

wherein

_EH^OM^O^|_| > _EH^OM^O Q) and the difference between the energy level of the highest occupied molecular orbital HOMO(E) of the organic molecule according to the invention E (E^HOMO(E)) and the energy level of the highest occupied molecular orbital HOMO(H) of the host compound H (E^HOMO(H)) is between -0.5 eV and 0.5 eV, more preferably between -0.3 eV and 0.3 eV, even more preferably between -0.2 eV and 0.2 eV or even between -0.1 eV and 0.1 eV; and _EL^UM^O |_| > _EL^UM^O Q) and the difference between the energy level of the lowest unoccupied molecular orbital LUMO(E) of the organic molecule according to the invention E (E^LUMO(E)) and the lowest unoccupied molecular orbital LUMO(D) of the at least one further host compound D (EL^UM^O(D)) is between -0.5 eV and 0.5 eV, more preferably between -0.3 eV and 0.3 eV, even more preferably between -0.2 eV and 0.2 eV or even between -0.1 eV and 0.1 eV.

In a further aspect, the invention relates to an optoelectronic device comprising an organic molecule or a composition of the type described here, more particularly in the form of a device selected from the group consisting of organic light-emitting diode (OLED), light-emitting electrochemical cell, OLED sensor, more particularly gas and vapour sensors not hermetically externally shielded, organic diode, organic solar cell, organic transistor, organic field-effect transistor, organic laser and down-conversion element.

In a preferred embodiment, the optoelectronic device is a device selected from the group consisting of an organic light emitting diode (OLED), a light emitting electrochemical cell (LEC), and a light-emitting transistor.

In one embodiment of the optoelectronic device of the invention, the organic molecule according to the invention E is used as emission material in a light-emitting layer EML.

In one embodiment of the optoelectronic device of the invention the light-emitting layer EML consists of the composition according to the invention described here.

Exemplarily, when the optoelectronic device is an OLED, it may exhibit the following layer structure:

1 . substrate

2. anode layer A

3. hole injection layer, HIL

4. hole transport layer, HTL

5. electron blocking layer, EBL

6. emitting layer, EML

7. hole blocking layer, HBL

8. electron transport layer, ETL

9. electron injection layer, EIL

10. cathode layer, wherein the OLED comprises each layer only optionally, different layers may be merged and the OLED may comprise more than one layer of each layer type defined above. Furthermore, the optoelectronic device may optionally comprise one or more protective layers protecting the device from damaging exposure to harmful species in the environment including, exemplarily moisture, vapor and/or gases.

In one embodiment of the invention, the optoelectronic device is an OLED, which exhibits the following inverted layer structure:

1 . substrate

2. cathode layer

3. electron injection layer, EIL

4. electron transport layer, ETL

5. hole blocking layer, HBL

6. emitting layer, B

7. electron blocking layer, EBL

8. hole transport layer, HTL

9. hole injection layer, HIL

10. anode layer A, wherein the OLED with an inverted layer structure comprises each layer only optionally, different layers may be merged and the OLED may comprise more than one layer of each layer types defined above.

In one embodiment of the invention, the optoelectronic device is an OLED, which may exhibit stacked architecture. In this architecture, contrary to the typical arrangement, where the OLEDs are placed side by side, the individual units are stacked on top of each other. Blended light may be generated with OLEDs exhibiting a stacked architecture, in particular white light may be generated by stacking blue, green and red OLEDs. Furthermore, the OLED exhibiting a stacked architecture may optionally comprise a charge generation layer (CGL), which is typically located between two OLED subunits and typically consists of a n-doped and p-doped layer with the n-doped layer of one CGL being typically located closer to the anode layer.

In one embodiment of the invention, the optoelectronic device is an OLED, which comprises two or more emission layers between anode and cathode. In particular, this so-called tandem OLED comprises three emission layers, wherein one emission layer emits red light, one emission layer emits green light and one emission layer emits blue light, and optionally may comprise further layers such as charge generation layers, blocking or transporting layers between the individual emission layers. In a further embodiment, the emission layers are adjacently stacked. In a further embodiment, the tandem OLED comprises a charge generation layer between each two emission layers. In addition, adjacent emission layers or emission layers separated by a charge generation layer may be merged.

The substrate may be formed by any material or composition of materials. Most frequently, glass slides are used as substrates. Alternatively, thin metal layers (e.g., copper, gold, silver or aluminum films) or plastic films or slides may be used. This may allow a higher degree of flexibility. The anode layer A is mostly composed of materials allowing to obtain an (essentially) transparent film. As at least one of both electrodes should be (essentially) transparent in order to allow light emission from the OLED, either the anode layer A or the cathode layer C is transparent. Preferably, the anode layer A comprises a large content or even consists of transparent conductive oxides (TCOs). Such anode layer A may, for example, comprise indium tin oxide, aluminum zinc oxide, fluorine doped tin oxide, indium zinc oxide, PbO, SnO, zirconium oxide, molybdenum oxide, vanadium oxide, wolfram oxide, graphite, doped Si, doped Ge, doped GaAs, doped polyaniline, doped polypyrrol and/or doped polythiophene.

The anode layer A (essentially) may consist of indium tin oxide (ITO) (e.g., (ln0₃)0.9(Sn0₂)0.1 ). The roughness of the anode layer A caused by the transparent conductive oxides (TCOs) may be compensated by using a hole injection layer (HIL). Further, the HIL may facilitate the injection of quasi charge carriers (i.e., holes) in that the transport of the quasi charge carriers from the TCO to the hole transport layer (HTL) is facilitated. The hole injection layer (HIL) may comprise poly-3, 4-ethylendioxy thiophene (PEDOT), polystyrene sulfonate (PSS), M0O2, V2O5, CuPC or Cul, in particular a mixture of PEDOT and PSS. The hole injection layer (HIL) may also prevent the diffusion of metals from the anode layer A into the hole transport layer (HTL). The HIL may, for example, comprise PEDOT:PSS (poly-3, 4- ethylendioxy thiophene: polystyrene sulfonate), PEDOT (poly-3, 4-ethylendioxy thiophene), mMTDATA (4,4',4"-tris[phenyl(m-tolyl)amino]triphenylamine), Spiro-TAD (2, 2', 7,7'- tetrakis(n,n-diphenylamino)-9,9’-spirobifluorene), DNTPD (N 1 ,NT-(biphenyl-4,4'-diyl)bis(N1 - phenyl-N4,N4-di-m-tolylbenzene-1 ,4-diamine), NPB (N,N'-nis-(1 -naphthalenyl)-N,N'-bis- phenyl-(1 ,T-biphenyl)-4,4'-diamine), NPNPB (N,N'-diphenyl-N,N'-di-[4-(N,N-diphenyl- amino)phenyl]benzidine), MeO-TPD (N,N,N',N'-tetrakis(4-methoxyphenyl)benzidine), HAT- CN (1 ,4, 5, 8, 9,1 1 -hexaazatriphenylen-hexacarbonitrile) and/or Spiro-NPD (N,N'-diphenyl-N,N'- bis-(1 -naphthyl)-9,9'-spirobifluorene-2, 7-diamine).

Adjacent to the anode layer A or hole injection layer (HIL), a hole transport layer (HTL) is typically located. Herein, any hole transport compound may be used. For example, electron- rich heteroaromatic compounds such as triarylamines and/or carbazoles may be used as hole transport compound. The HTL may decrease the energy barrier between the anode layer A and the light-emitting layer EML. The hole transport layer (HTL) may also be an electron blocking layer (EBL). Preferably, hole transport compounds bear comparably high energy levels of their triplet states T1. For example, the hole transport layer (HTL) may comprise a star-shaped heterocycle such as tris(4-carbazoyl-9-ylphenyl)amine (TCTA), poly-TPD (poly(4- butylphenyl-diphenyl-amine)), [alpha]-NPD (poly(4-butylphenyl-diphenyl-amine)), TAPC (4,4 - cyclohexyliden-bis[N,N-bis(4-methylphenyl)benzenamine]), 2-TNATA (4,4',4"-tris[2- naphthyl(phenyl)amino]triphenylamine), Spiro-TAD, DNTPD, NPB, NPNPB, MeO-TPD, HAT- CN and/or TrisPcz (9,9'-diphenyl-6-(9-phenyl-9H-carbazol-3-yl)-9H,9'H-3,3'-bicarbazole). In addition, the HTL may comprise a p-doped layer, which may be composed of an inorganic or organic dopant in an organic hole-transporting matrix. Transition metal oxides such as vanadium oxide, molybdenum oxide or tungsten oxide may exemplarily be used as inorganic dopant. Tetrafluorotetracyanoquinodimethane (F₄-TCNQ), copper-pentafluorobenzoate (Cu(l)pFBz) or transition metal complexes may exemplarily be used as organic dopant.

The EBL may exemplarily comprise mCP (1 ,3-bis(carbazol-9-yl)benzene), TCTA, 2-TNATA, mCBP (3,3-di(9H-carbazol-9-yl)biphenyl), tris-Pcz, CzSi (9-(4-tert-Butylphenyl)-3,6- bis(triphenylsilyl)-9H-carbazole), and/or DCB (N,N'-dicarbazolyl-1 ,4-dimethylbenzene).

Adjacent to the hole transport layer (HTL), typically, the light-emitting layer EML is located. The light-emitting layer EML comprises at least one light emitting molecule. Particularly, the EML comprises at least one light emitting molecule according to the invention E. In one embodiment, the light-emitting layer comprises only the organic molecules according to the invention E. Typically, the EML additionally comprises one or more host materials H. Exemplarily, the host material H is selected from CBP (4,4'-Bis-(N-carbazolyl)-biphenyl), mCP, mCBP Sif87 (dibenzo[b,d]thiophen-2-yltriphenylsilane), CzSi, Sif88 (dibenzo[b,d]thiophen-2- yl)diphenylsilane), DPEPO (bis[2-(diphenylphosphino)phenyl] ether oxide), 9-[3- (dibenzofuran-2-yl)phenyl]-9H-carbazole, 9-[3-(dibenzofuran-2-yl)phenyl]-9H-carbazole, 9-[3- (dibenzothiophen-2-yl)phenyl]-9H-carbazole, 9-[3,5-bis(2-dibenzofuranyl)phenyl]-9H- carbazole, 9-[3,5-bis(2-dibenzothiophenyl)phenyl]-9H-carbazole, T2T (2,4,6-tris(biphenyl-3- yl)-1 ,3,5-triazine), T3T (2,4,6-tris(triphenyl-3-yl)-1 ,3,5-triazine) and/or TST (2,4,6-tris(9,9'- spirobifluorene-2-yl)-1 ,3,5-triazine). The host material H typically should be selected to exhibit first triplet (T 1 ) and first singlet (S1 ) energy levels, which are energetically higher than the first triplet (T 1 ) and first singlet (S1 ) energy levels of the organic molecule.

In one embodiment of the invention, the EML comprises a so-called mixed-host system with at least one hole-dominant host and one electron-dominant host. In a particular embodiment, the EML comprises exactly one light emitting molecule according to the invention E and a mixed-host system comprising T2T as electron-dominant host and a host selected from CBP, mCP, mCBP, 9-[3-(dibenzofuran-2-yl)phenyl]-9H-carbazole, 9-[3-(dibenzofuran-2-yl)phenylj- 9H-carbazole, 9-[3-(dibenzothiophen-2-yl)phenyl]-9H-carbazole, 9-[3,5-bis(2- dibenzofuranyl)phenyl]-9H-carbazole and 9-[3,5-bis(2-dibenzothiophenyl)phenyl]-9H- carbazole as hole-dominant host. In a further embodiment the EML comprises 50-80 % by weight, preferably 60-75 % by weight of a host selected from CBP, mCP, mCBP, 9-[3- (dibenzofuran-2-yl)phenyl]-9H-carbazole, 9-[3-(dibenzofuran-2-yl)phenyl]-9H-carbazole, 9-[3- (dibenzothiophen-2-yl)phenyl]-9H-carbazole, 9-[3,5-bis(2-dibenzofuranyl)phenyl]-9H- carbazole and 9-[3,5-bis(2-dibenzothiophenyl)phenyl]-9H-carbazole; 10-45 % by weight, preferably 15-30 % by weight of T2T and 5-40 % by weight, preferably 10-30 % by weight of light emitting molecule according to the invention.

Adjacent to the light-emitting layer EML an electron transport layer (ETL) may be located. Herein, any electron transporter may be used. Exemplarily, electron-poor compounds such as, e.g., benzimidazoles, pyridines, triazoles, oxadiazoles (e.g., 1 ,3,4-oxadiazole), phosphinoxides and sulfone, may be used. An electron transporter may also be a star-shaped heterocycle such as 1 , 3, 5-tri(1 -phenyl-1 H-benzo[d]imidazol-2-yl)phenyl (TPBi). The ETL may comprise NBphen (2,9-bis(naphthalen-2-yl)-4,7-diphenyl-1 ,10-phenanthroline), Alq3 (Aluminum-tris(8-hydroxyquinoline)), TSP01 (diphenyl-4-triphenylsilylphenyl-phosphinoxide), BPyTP2 (2,7-di(2,2'-bipyridin-5-yl)triphenyle), Sif87 (dibenzo[b,d]thiophen-2-yltriphenylsilane), Sif88 (dibenzo[b,d]thiophen-2-yl)diphenylsilane), BmPyPhB (1 ,3-bis[3,5-di(pyridin-3- yl)phenyl]benzene) and/or BTB (4, 4'-bis-[2-(4,6-diphenyl-1 , 3, 5-triazinyl)]-1 ,1 -biphenyl). Optionally, the ETL may be doped with materials such as Liq. The electron transport layer (ETL) may also block holes or a holeblocking layer (HBL) is introduced.

The HBL may, for example, comprise BCP (2,9-dimethyl-4,7-diphenyl-1 ,10-phenanthroline = Bathocuproine), BAIq (bis(8-hydroxy-2-methylquinoline)-(4-phenylphenoxy)aluminum), NBphen (2, 9-bis(naphthalen-2-yl)-4,7-diphenyl-1 ,10-phenanthroline), Alq3 (Aluminum-tris(8- hydroxyquinoline)), TSP01 (diphenyl-4-triphenylsilylphenyl-phosphinoxide), T2T (2,4,6- tris(biphenyl-3-yl)-1 ,3,5-triazine), T3T (2,4,6-tris(triphenyl-3-yl)-1 ,3,5-triazine), TST (2,4,6- tris(9,9'-spirobifluorene-2-yl)-1 ,3,5-triazine), and/or TCB/TCP (1 ,3,5-tris(N-carbazolyl)benzol/ 1 ,3,5-tris(carbazol)-9-yl) benzene).

Adjacent to the electron transport layer (ETL), a cathode layer C may be located. For example, the cathode layer C may comprise or may consist of a metal (e.g., Al, Au, Ag, Pt, Cu, Zn, Ni, Fe, Pb, LiF, Ca, Ba, Mg, In, W, or Pd) or a metal alloy. For practical reasons, the cathode layer may also consist of (essentially) intransparent metals such as Mg, Ca or Al. Alternatively or additionally, the cathode layer C may also comprise graphite and or carbon nanotubes (CNTs). Alternatively, the cathode layer C may also consist of nanoscalic silver wires.

An OLED may further, optionally, comprise a protection layer between the electron transport layer (ETL) and the cathode layer C (which may be designated as electron injection layer (EIL)). This layer may comprise lithium fluoride, cesium fluoride, silver, Liq (8- hydroxyquinolinolatolithium), LhO, BaF2, MgO and/or NaF.

Optionally, also the electron transport layer (ETL) and/or a hole blocking layer (HBL) may comprise one or more host compounds H.

In order to modify the emission spectrum and/or the absorption spectrum of the light-emitting layer EML further, the light-emitting layer EML may further comprise one or more further emitter molecules F. Such an emitter molecule F may be any emitter molecule known in the art. Preferably such an emitter molecule F is a molecule with a structure differing from the structure of the molecules according to the invention E. The emitter molecule F may optionally be a TADF emitter. Alternatively, the emitter molecule F may optionally be a fluorescent and/or phosphorescent emitter molecule which is able to shift the emission spectrum and/or the absorption spectrum of the light-emitting layer EML. Exemplarily, the triplet and/or singlet excitons may be transferred from the emitter molecule according to the invention E to the emitter molecule F before relaxing to the ground state SO by emitting light typically red-shifted in comparison to the light emitted by emitter molecule E. Optionally, the emitter molecule F may also provoke two-photon effects (i.e., the absorption of two photons of half the energy of the absorption maximum).

Optionally, an optoelectronic device (e.g., an OLED) may, for example, be an essentially white optoelectronic device. For example, such a white optoelectronic device may comprise at least one (deep) blue emitter molecule and one or more emitter molecules emitting green and/or red light. Then, there may also optionally be energy transmittance between two or more molecules as described above.

As used herein, if not defined more specifically in the particular context, the designation of the colors of emitted and/or absorbed light is as follows: violet: wavelength range of >380-420 nm;

deep blue: wavelength range of >420-480 nm;

sky blue: wavelength range of >480-500 nm; green: wavelength range of >500-560 nm;

yellow: wavelength range of >560-580 nm;

orange: wavelength range of >580-620 nm;

red: wavelength range of >620-800 nm.

With respect to emitter molecules, such colors refer to the emission maximum. Therefore, for example, a deep blue emitter has an emission maximum in the range of from >420 to 480 nm, a sky blue emitter has an emission maximum in the range of from >480 to 500 nm, a green emitter has an emission maximum in a range of from >500 to 560 nm, a red emitter has an emission maximum in a range of from >620 to 800 nm.

A deep blue emitter may preferably have an emission maximum of below 480 nm, more preferably below 470 nm, even more preferably below 465 nm or even below 460 nm. It will typically be above 420 nm, preferably above 430 nm, more preferably above 440 nm or even above 450 nm.

Accordingly, a further aspect of the present invention relates to an OLED, which exhibits an external quantum efficiency at 1000 cd/m² of more than 8 %, more preferably of more than 10 %, more preferably of more than 13 %, even more preferably of more than 15 % or even more than 20 % and/or exhibits an emission maximum between 420 nm and 500 nm, preferably between 430 nm and 490 nm, more preferably between 440 nm and 480 nm, even more preferably between 450 nm and 470 nm and/or exhibits a LT80 value at 500 cd/m² of more than 100 h, preferably more than 200 h, more preferably more than 400 h, even more preferably more than 750 h or even more than 1000 h. Accordingly, a further aspect of the present invention relates to an OLED, whose emission exhibits a CIEy color coordinate of less than 0.45, preferably less than 0.30, more preferably less than 0.20 or even more preferably less than 0.15 or even less than 0.10.

A further aspect of the present invention relates to an OLED, which emits light at a distinct color point. According to the present invention, the OLED emits light with a narrow emission band (small full width at half maximum (FWHM)). In one aspect, the OLED according to the invention emits light with a FWHM of the main emission peak of less than 0.50 eV, preferably less than 0.48 eV, more preferably less than 0.45 eV, even more preferably less than 0.43 eV or even less than 0.40 eV.

A further aspect of the present invention relates to an OLED, which emits light with Cl Ex and CIEy color coordinates close to the CIEx (= 0.131 ) and CIEy (= 0.046) color coordinates of the primary color blue (CIEx = 0.131 and CIEy = 0.046) as defined by ITU-R Recommendation BT.2020 (Rec. 2020) and thus is suited for the use in Ultra High Definition (UHD) displays, e.g. UHD-TVs. Accordingly, a further aspect of the present invention relates to an OLED, whose emission exhibits a CIEx color coordinate of between 0.02 and 0.30, preferably between 0.03 and 0.25, more preferably between 0.05 and 0.20 or even more preferably between 0.08 and 0.18 or even between 0.10 and 0.15 and / or a a CIEy color coordinate of between 0.00 and 0.45, preferably between 0.01 and 0.30, more preferably between 0.02 and 0.20 or even more preferably between 0.03 and 0.15 or even between 0.04 and 0.10.

In a further aspect, the invention relates to a method for producing an optoelectronic device. In this case an organic molecule of the invention is used.

The optoelectronic device, in particular the OLED according to the present invention can be fabricated by any means of vapor deposition and / or liquid processing. Accordingly, at least one layer is

prepared by means of a sublimation process,

prepared by means of an organic vapor phase deposition process,

prepared by means of a carrier gas sublimation process,

solution processed or printed.

The methods used to fabricate the optoelectronic device, in particular the OLED according to the present invention are known in the art. The different layers are individually and successively deposited on a suitable substrate by means of subsequent deposition processes. The individual layers may be deposited using the same or differing deposition methods.

Vapor deposition processes may comprise thermal (co)evaporation, chemical vapor deposition and physical vapor deposition. For active matrix OLED display, an AMOLED backplane is used as substrate. The individual layer may be processed from solutions or dispersions employing adequate solvents. Solution deposition process exemplarily comprise spin coating, dip coating and jet printing. Liquid processing may optionally be carried out in an inert atmosphere (e.g., in a nitrogen atmosphere) and the solvent may optionally be completely or partially removed by means known in the state of the art. Examples

General synthesis scheme I

General procedure for synthesis AAV1\

3-Bromo-4-fluorophenylbenzonitrile (1 .00 equivalent, CAS 79630-23-2), bis- (pinacolato)diboron (1 .5 equivalents, CAS 73183-34-3), tris(dibenzylideneacetone)dipalladium(0) Pd₂(dba)₃ (0.04 equivalents, CAS 51364-51 -3), X-Phos (0.08 equivalents, CAS 564483-18-7) and potassium acetate (KOAc, 3.0 equivalents) are stirred under nitrogen atmosphere in dry toluene at 1 10 °C for 16 h. After cooling down to room temperature (RT) the reaction mixture is extracted with ethyl acetate/brine. The organic phases are collected, washed with brine and dried over MgS0₄. The organic solvent is removed, the crude product was washed with cyclohexane and recrystallized from EtOH.

General procedure for synthesis AAV2\

E1 (1 .00 equivalent), 4-bromo-2,3-difluorobenzonitrile (1 equivalent; CAS 126163-58-4), tris(dibenzylideneacetone)dipalladium(0) Pd₂(dba)₃ (0.04 equivalents; CAS 51364-51 -3), X-Phos (0.08 equivalents, CAS 564483-18-7) and potassium phosphate (K3PO4, 3.0 equivalents) are stirred under nitrogen atmosphere in dry toluene/H20 (10:1 ) at 100 °C for 16 h. After cooling down to room temperature (RT) and the reaction mixture is extracted with ethyl acetate/brine. Organic phase is collected, washed with brine and dried over MgS0₄. The organic solvent is removed, the crude product was washed with cyclohexane and recrystallized from EtOH.

General procedure for synthesis AAV3:

1 10 C, toluene/water

E1 Z2

E1 (1 .00 equivalent), 4-bromo-2,6-difluorobenzonitrile (1 equivalent; CAS 123843-67-4), tris(dibenzylideneacetone)dipalladium(0) Pd₂(dba)₃ (0.04 equivalents; CAS 51364-51 -3), X-Phos (0.08 equivalents, CAS 564483-18-7) and potassium phosphate (K3PO4, 3.0 equivalents) are stirred under nitrogen atmosphere in dry toluene/H20 (10:1 ) at 100 °C for 16 h. After cooling down to room temperature (RT) and the reaction mixture is extracted with ethyl acetate/brine. Organic phase is collected, washed with brine and dried over MgS0₄. The organic solvent is removed, the crude product is directly used in the next step without further purification.

General procedure for synthesis AAV4\

1 10°C, toluene E2

4-Bromo-2,3-difluorobenzonitrile (1 .00 equivalent, CAS 126163-58-4), bis-(pinacolato)diboron (1 .5 equivalents, CAS 73183-34-3), tris(dibenzylideneacetone)dipalladium(0) Pd₂(dba)₃ (0.04 equivalents, CAS 51364-51 -3), X-Phos (0.08 equivalents, CAS 564483-18-7) and potassium acetate (KOAc, 3.0 equivalents) are stirred under nitrogen atmosphere in dry toluene at 1 10 °C for 16 h. After cooling down to room temperature (RT) the reaction mixture is extracted with ethyl acetate/brine. The organic phases are collected, washed with brine and dried over MgS0₄. The organic solvent is removed, the crude product was washed with cyclohexane and recrystallized from EtOH.

General procedure for synthesis AAV5\

E2 1 10°C, toluene Z1

E2 (1 .00 equivalent), 3-Bromo-4-fluorophenylbenzonitrile (1 .00 equivalent, CAS 79630-23-2), tris(dibenzylideneacetone)dipalladium(0) Pd₂(dba)₃ (0.04 equivalents, CAS 51364-51 -3), X-Phos (0.08 equivalents, CAS 564483-18-7) and potassium acetate (KOAc, 3.0 equivalents) are stirred under nitrogen atmosphere in dry toluene at 1 10 °C for 16 h. After cooling down to room temperature (RT) the reaction mixture is extracted with ethyl acetate/brine. The organic phases are collected, washed with brine and dried over MgS0₄. The organic solvent is removed, the crude product was washed with cyclohexane and recrystallized from EtOH.

General procedure for synthesis AAV6\

1 10 C, toluene E3

4-bromo-2,6-difluorobenzonitrile (1 equivalent; CAS 123843-67-4), bis-(pinacolato)diboron (1 .5 equivalents, CAS 73183-34-3), tris(dibenzylideneacetone)dipalladium(0) Pd₂(dba)₃ (0.04 equivalents, CAS 51364-51 -3), X-Phos (0.08 equivalents, CAS 564483-18-7) and potassium acetate (KOAc, 3.0 equivalents) are stirred under nitrogen atmosphere in dry toluene at 1 10 °C for 16 h. After cooling down to room temperature (RT) the reaction mixture is extracted with ethyl acetate/brine. The organic phases are collected, washed with brine and dried over MgS0₄. The organic solvent is removed, the crude product was washed with cyclohexane and recrystallized from EtOH.

General procedure for synthesis AAV7\

E3 (1.00 equivalent), 3-Bromo-4-fluorophenylbenzonitrile (1.00 equivalent, CAS 79630-23-2), tris(dibenzylideneacetone)dipalladium(0) Pd₂(dba)₃ (0.04 equivalents, CAS 51364-51-3), X-Phos (0.08 equivalents, CAS 564483-18-7) and potassium acetate (KOAc, 3.0 equivalents) are stirred under nitrogen atmosphere in dry toluene at 110 °C for 16 h. After cooling down to room temperature (RT) the reaction mixture is extracted with ethyl acetate/brine. The organic phases are collected, washed with brine and dried over MgS0₄. The organic solvent is removed, the crude product was washed with cyclohexane and recrystallized from EtOH.

Z1 or Z2 (1 equivalent each), the corresponding donor molecule D-H (3.20 equivalents) and tribasic potassium phosphate (3.00 equivalents) are suspended under nitrogen atmosphere in DMSO and stirred at 120 °C (16 h). After cooling to room temperature the reaction mixture is extracted with ethyl acetate/brine. Organic phases are collected, washed with brine and dried over MgS0₄. The solvents are remove under reduced pressure. The crude product is purified by recrystallization or by flash chromatography.

In particular, the donor molecule D-H is a 3,6-substituted carbazole (e.g., 3,6- dimethylcarbazole, 3,6-diphenylcarbazole, 3,6-di-tert-butylcarbazole), a 2,7-substituted carbazole (e.g., 2,7-dimethylcarbazole, 2,7-diphenylcarbazole, 2,7-di-tert-butylcarbazole), a 1 ,8-substituted carbazole (e.g., 1 ,8-dimethylcarbazole, 1 ,8-diphenylcarbazole, 1 ,8-di-tert- butylcarbazole), a 1 -substituted carbazole (e.g., 1 -methylcarbazole, 1 -phenylcarbazole, 1 -tert- butylcarbazole), a 2-substituted carbazole (e.g., 2-methylcarbazole, 2-phenylcarbazole, 2-tert- butylcarbazole), or a 3-substituted carbazole (e.g., 3-methylcarbazole, 3-phenylcarbazole, 3- tert-butylcarbazole).

Exemplarily, a halogen-substituted carbazole, particularly 3-bromocarbazole, can be used as

D-H.

In a subsequent reaction, a boronic acid ester functional group or boronic acid functional group may be, for example, introduced at the position of the one or more halogen substituents, which was introduced via D-H, to yield the corresponding carbazol-3-ylboronic acid ester or carbazol- 3-ylboronic acid, e.g., via the reaction with bis(pinacolato)diboron (CAS No. 73183-34-3). Subsequently, one or more substituents R^a may be introduced in place of the boronic acid ester group or the boronic acid group via a coupling reaction with the corresponding halogenated reactant R^a-Hal, preferably R^a-CI and R^a-Br. Alternatively, one or more substituents R^a may be introduced at the position of the one or more halogen substituents, which was introduced via D-H, via the reaction with a boronic acid of the substituent R^a [R^a-B(OH)2] or a corresponding boronic acid ester.

Cyclic voltammetry

Cyclic voltammograms are measured from solutions having concentration of 10 ³ mol/L of the organic molecules in dichloromethane or a suitable solvent and a suitable supporting electrolyte (e.g. 0.1 mol/L of tetrabutylammonium hexafluorophosphate). The measurements are conducted at room temperature under nitrogen atmosphere with a three-electrode assembly (Working and counter electrodes: Pt wire, reference electrode: Pt wire) and calibrated using FeCp2/FeCp2⁺ as internal standard. The HOMO data was corrected using ferrocene as internal standard against SCE (englisch: saturated calomel electrode).

Density functional theory calculation

Molecular structures are optimized employing the BP86 functional and the resolution of identity approach (Rl). Excitation energies are calculated using the (BP86) optimized structures employing Time-Dependent DFT (TD-DFT) methods. Orbital and excited state energies are calculated with the B3LYP functional. Def2-SVP basis sets (and a m4-grid for numerical integration are used. The Turbomole program package is used for all calculations.

Photophysical measurements

Sample pretreatment: Spin-coating

Apparatus: Spin150, SPS euro.

The sample concentration is 10 mg/ml, dissolved in a suitable solvent.

Program: 1 ) 3 s at 400 U/min; 20 s at 1000 U/min at 1000 Upm/s. 3) 10 s at 4000 U/min at 1000 Upm/s. After coating, the films are tried at 70 °C for 1 min.

Photoluminescence spectroscopy and TCSPC (Time-correlated single-photon counting) Steady-state emission spectroscopy is measured by a Horiba Scientific, Modell FluoroMax-4 equipped with a 150 W Xenon-Arc lamp, excitation- and emissions monochromators and a Hamamatsu R928 photomultiplier and a time-correlated single-photon counting option. Emissions and excitation spectra are corrected using standard correction fits.

Excited state lifetimes are determined employing the same system using the TCSPC method with FM-2013 equipment and a Horiba Yvon TCSPC hub.

Excitation sources:

NanoLED 370 (wavelength: 371 nm, puls duration: 1 ,1 ns)

NanoLED 290 (wavelength: 294 nm, puls duration: <1 ns)

SpectraLED 310 (wavelength: 314 nm) SpectraLED 355 (wavelength: 355 nm).

Data analysis (exponential fit) is done using the software suite DataStation and DAS6 analysis software. The fit is specified using the chi-squared-test.

Photoluminescence quantum yield measurements

For photoluminescence quantum yield (PLQY) measurements an Absolute PL Quantum Yield Measurement C9920-03G system ( Hamamatsu Photonics) is used. Quantum yields and CIE coordinates are determined using the software U6039-05 version 3.6.0.

Emission maxima are given in nm, quantum yields F in % and CIE coordinates as x,y values. PLQY is determined using the following protocol:

1 ) Quality assurance: Anthracene in ethanol (known concentration) is used as reference

2) Excitation wavelength: the absorption maximum of the organic molecule is determined and the molecule is excited using this wavelength

3) Measurement

Quantum yields are measured for sample of solutions or films under nitrogen atmosphere. The yield is calculated using the equation:

wherein n_Photon denotes the photon count and Int. the intensity.

Production and characterization of optoelectronic devices

OLED devices comprising organic molecules according to the invention can be produced via vacuum-deposition methods. If a layer contains more than one compound, the weight- percentage of one or more compounds is given in %. The total weight-percentage values amount to 100 %, thus if a value is not given, the fraction of this compound equals to the difference between the given values and 100 %.

The not fully optimized OLEDs are characterized using standard methods and measuring electroluminescence spectra, the external quantum efficiency (in %) in dependency on the intensity, calculated using the light detected by the photodiode, and the current. The OLED device lifetime is extracted from the change of the luminance during operation at constant current density. The LT50 value corresponds to the time, where the measured luminance decreased to 50 % of the initial luminance, analogously LT80 corresponds to the time point, at which the measured luminance decreased to 80 % of the initial luminance, LT 95 to the time point, at which the measured luminance decreased to 95 % of the initial luminance etc.

Accelerated lifetime measurements are performed (e.g. applying increased current densities). Exemplarily LT80 values at 500 cd/m² are determined using the following equation: / L

LT80 ( 500

\ c

500

wherein Lo denotes the initial luminance at the applied current density.

The values correspond to the average of several pixels (typically two to eight), the standard deviation between these pixels is given.

HPLC-MS

HPLC-MS spectroscopy is performed on a HPLC by Agilent (1 100 series) with MS-detector (Thermo LTQ XL).

Exemplarily a typical HPLC method is as follows: a reverse phase column 4.6 mm x 150 mm, particle size 3.5 pm from Agilent (ZORBAX Eclipse Plus 95A C18, 4.6 x 150 mm, 3.5 pm HPLC column) is used in the HPLC. The HPLC-MS measurements are performed at room temperature (rt) following gradients:

Flow rate [ml/minl Time [min] A[%] B[%] C[%]

2.5 0 40 50 10

2.5 5 40 50 10

2.5 25 10 20 70

2.5 35 10 20 70

2.5 35.01 40 50 10

2.5 40.01 40 50 10

2.5 41.01 40 50 10 using the following solvent mixtures

An injection volume of 5 pL from a solution with a concentration of 0.5 mg/mL of the analyte is taken for the measurements.

Ionization of the probe is performed using an atmospheric pressure chemical ionization (APCI) source either in positive (APCI +) or negative (APCI -) ionization mode. Example 1

Example 1 was synthesized according to AAV1 (yield = 64%), AAV2 (yield = 42%) and AAV8 (yield = 92 %).

HPLC-MS: 715.40 m/z, 100 %.

¹H NMR (500 MHz, DMSO-de) d 9.27 (d, J = 2.1 Hz, 1 H), 8.85 - 8.76 (m, 4H), 8.68 (dd, J = 8.3, 2.0 Hz, 1 H), 8.25 (dd, J = 7.9, 1 .5 Hz, 1 H), 7.92 (s, 3H), 7.80 - 7.68 (m, 8H), 7.47 (td, J = 7.7, 1 .6 Hz, 1 H), 7.30 (d, J = 8.3 Hz, 1 H), 7.25 - 6.50 (m, 1 1 H), 5.71 (s, 2H).

Figure 1 depicts the emission spectrum of example 1 (10 % by weight in PMMA). The emission maximum (A_max) is at 494 nm. The photoluminescence quantum yield (PLQY) is 89%, the full width at half maximum (FWHM) is 0.39 eV and the emission lifetime is 4 ps. The energy of the highest occupied molecular orbital (E^homo) is -5.76 eV.

Example 2

Example 2 was synthesized according to AAV1 (yield = 64%), AAV2 (yield = 42%) and AAV8 (yield = 45 %).

HPLC-MS: 791 .68 m/z.

Figure 2 depicts the emission spectrum of example 2 (10 % by weight in PMMA). The emission maximum (A_max) is at 490 nm. The photoluminescence quantum yield (PLQY) is 86%, the full width at half maximum (FWHM) is 0.41 eV and the emission lifetime is 5 ps. The energy of the highest occupied molecular orbital (E^homo) is -5.85 eV.

Example 3

Example 3 was synthesized according to AAV6 (yield = 35%), AAV7 (yield = 82%) and AAV8 (yield = 15%).

HPLC-MS: 1036.9 m/z.

Figure 3 depicts the emission spectrum of example 3 (10 % by weight in PMMA). The emission maximum (A_max) is at 466 nm. The photoluminescence quantum yield (PLQY) is 83%, the full width at half maximum (FWHM) is 0.42 eV and the emission lifetime is 25 ps. The energy of the highest occupied molecular orbital (E^homo) is -6.05 eV. Example 4

Example 4 was synthesized according to AAV3 (yield = 89%) and AAV8 (yield = 78%).

HPLC-MS: 700.40 m/z.

Figure 4 depicts the emission spectrum of example 4 (10 % by weight in PMMA). The emission maximum (A_max) is at 466 nm. The photoluminescence quantum yield (PLQY) is 64%, the full width at half maximum (FWHM) is 0.50 eV and the CIEy coordinate is 0.20. The energy of the highest occupied molecular orbital (E^homo) is -6.19 eV.

Example 5

Example 5 was synthesized via the following synthesis route: Based on the conditions of

AAV8, the introduction of the substituted carbazole

was carried out leading

(yield = 92%). In two further steps, AAV7 (yield = 31 %) and AAV8 (yield = 74%) were carried out to obtain example 5 as the final product.

HPLC-MS: 851 .30 m/z.

Figure 5 depicts the emission spectrum of example 5 (10 % by weight in PMMA). The emission maximum (A_max) is at 468 nm and the CIEy coordinate is 0.21. The photoluminescence quantum yield (PLQY) is 65%, the full width at half maximum (FWHM) is 0.44 eV and the emission lifetime is 83 ps.

Example D1

Example 3 was tested in the OLED D1 , which was fabricated with the following layer structure:

MAT1

Device D1 yielded an external quantum efficiency (EQE) at 1000 cd/m² of 13.1 ± 0.3%. The emission maximum is at 475 nm with a FWHM of 66 nm at 10.0 V. The corresponding CIEx value is 0.15 and CIEy is 0.25. Additional Examples of Organic Molecules of the Invention

55







Figures

Figure 1 Emission spectrum of example 1 (10% by weight) in PMMA.

Figure 2 Emission spectrum of example 2 (10% by weight) in PMMA.

Figure 3 Emission spectrum of example 3 (10% by weight) in PMMA.

Figure 4 Emission spectrum of example 4 (10% by weight) in PMMA.

Figure 5 Emission spectrum of example 5 (10% by weight) in PMMA.

Claims

1 . Organic molecule, comprising

- one first chemical moiety comprising a structure of formula I,

Formula I

and

- three second chemical moieties, each independently from another comprising a structure of formula II,

Formula II wherein the first chemical moiety is linked to each of the three second chemical moieties via a single bond;

wherein

T is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹;

V is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹;

W is CN;

X is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹;

Y is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹;

R^T is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties;

R^v is R'; R^w is R¹;

R^x is CN;

R^Y is R¹;

# represents the binding site of a single bond linking the second chemical moieties to the first chemical moiety;

R¹ is at each occurrence independently from another selected from the group consisting of: hydrogen, deuterium,

Ci-C5-alkyl,

wherein one or more hydrogen atoms are optionally substituted by deuterium;

C₂-C₈-alkenyl,

wherein one or more hydrogen atoms are optionally substituted by deuterium;

C₂-C₈-alkynyl,

which is optionally substituted with one or more substituents R⁶;

R' is at each occurrence independently from another selected from the group consisting of: hydrogen, deuterium,

Ci-C5-alkyl,

wherein one or more hydrogen atoms are optionally substituted by deuterium;

C2-Cs-alkenyl,

wherein one or more hydrogen atoms are optionally substituted by deuterium;

C2-Cs-alkynyl,

which is optionally substituted with one or more substituents R⁶;

R^a, R³ and R⁴ is at each occurrence independently from another selected from the group consisting of: hydrogen, deuterium, N(R⁵)2, OR⁵, Si(R⁵)₃, B(OR⁵)2, OSO2R⁵, CF₃, CN, F, Br, I, Ci-C₄o-alkyl,

which is optionally substituted with one or more substituents R⁵ and

wherein one or more non-adjacent CFh-groups are optionally substituted by R⁵C=CR⁵, CºC, Si(R⁵)₂, Ge(R⁵)₂, Sn(R⁵)₂, C=0, C=S, C=Se, C=NR⁵, P(=0)(R⁵), SO, S0₂, NR⁵, O, S or CONR⁵; Ci-C4o-alkoxy,

which is optionally substituted with one or more substituents R⁵ and

Ci-C₄o-thioalkoxy,

which is optionally substituted with one or more substituents R⁵ and

C₂-C₄o-alkenyl,

which is optionally substituted with one or more substituents R⁵ and

C₂-C₄o-alkynyl,

which is optionally substituted with one or more substituents R⁵ and

Ce-Ceo-aryl,

which is optionally substituted with one or more substituents R⁵; and

C3-C57-heteroaryl,

which is optionally substituted with one or more substituents R⁵;

R⁵ is at each occurrence independently from another selected from the group consisting of hydrogen, deuterium, N(R⁶)₂, OR⁶, Si(R⁶)₃, B(OR⁶)₂, 0S0₂R⁶, CF₃, CN, F, Br, I,

Ci-C₄o-alkyl,

which is optionally substituted with one or more substituents R⁶ and

Ci-C₄o-alkoxy,

which is optionally substituted with one or more substituents R⁶ and

Ci-C₄o-thioalkoxy, which is optionally substituted with one or more substituents R⁶ and

C₂-C4o-alkenyl,

which is optionally substituted with one or more substituents R⁶ and

C₂-C₄o-alkynyl,

which is optionally substituted with one or more substituents R⁶ and

Ce-Ceo-aryl,

which is optionally substituted with one or more substituents R⁶; and

C3-C57-heteroaryl,

which is optionally substituted with one or more substituents R⁶;

R⁶ is at each occurrence independently from another selected from the group consisting of: hydrogen, deuterium, OPh, CF3, CN, F,

Ci-C5-alkyl,

wherein one or more hydrogen atoms are optionally, independently from each other substituted by deuterium, CN, CF3, or F;

Ci-Cs-alkoxy,

Ci-Cs-thioalkoxy,

C₂-C5-alkenyl,

C₂-C5-alkynyl,

Ce-Cis-aryl, which is optionally substituted with one or more C-i-Cs-alkyl substituents; C₃-Ci₇-heteroaryl,

which is optionally substituted with one or more C-i-Cs-alkyl substituents;

N(C6-Ci8-aryl)2;

N(C3-Ci7-heteroaryl)2,

and N(C₃-Ci₇-heteroaryl)(C₆-Ci₈-aryl); wherein the substituents R^a, R³, R⁴ or R⁵ independently from each other optionally form a mono- or polycyclic, aliphatic, aromatic and/or benzo-fused ring system with one or more substituents R^a, R³, R⁴ or R⁵;

wherein the terms alkyl, alkenyl, alkynyl, alkoxy and thioalkoxy can refer to linear, branched, and cyclic substituents; wherein

exactly two substituents selected from the group consisting of T, V, X and Y represent the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties.

2. Organic molecule according to claim 1 , wherein the first chemical moiety comprises a structure of Formula la:

Formula la

wherein

X^m is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties or is R¹, R^T is the binding site of a single bond linking the first chemical moiety to one of the three second chemical moieties,

wherein exactly two substituents selected from the group consisting of X", V^m and T^m represent the binding site of a single bond linking the first chemical moiety and one of the three second chemical moieties;

and wherein apart from that the definitions in claim 1 apply.

3. Organic molecule according to claim 1 or 2, wherein the first chemical moiety comprises a structure of formula laa:

Formula laa

wherein

and wherein apart from that the definitions in claim 1 apply.

4. Organic molecule according to one or more of claims 1 to 3, wherein R' and R¹ is independently from each other selected from the group of consisting of hydrogen (H), methyl, mesityl, tolyl, and phenyl.

5. Organic molecule according to one or more of claims 1 to 4, wherein the three second chemical moieties each at each occurrence, independently from another, comprise a structure of formula I la:

Formula lla wherein # and R^a are defined as in claim 1.

6. Organic molecule according to one or more of claims 1 to 5, wherein the three second chemical moieties each at each occurrence, independently from another, comprise a structure of formula lib:

Formula lib wherein

R^b is at each occurrence independently from another selected from the group consisting of: H, deuterium, N(R⁵)₂, OR⁵, Si(R⁵)₃, B(OR⁵)₂, 0S0₂R⁵, CF₃, CN, F, Br, I,

Ci-C₄o-alkyl,

which is optionally substituted with one or more substituents R⁵ and

Ci-C₄o-alkoxy,

which is optionally substituted with one or more substituents R⁵, and

Ci-C₄o-thioalkoxy,

which is optionally substituted with one or more substituents R⁵, and

C₂-C₄o-alkenyl,

which is optionally substituted with one or more substituents R⁵, and wherein one or more non-adjacent CH₂-groups are optionally substituted by R⁵C=CR⁵, CºC, Si(R⁵)₂, Ge(R⁵)₂, Sn(R⁵)₂, C=0, C=S, C=Se, C=NR⁵, P(=0)(R⁵), SO, S0₂, NR⁵, O, S or CONR⁵;

C₂-C₄o-alkynyl,

which is optionally substituted with one or more substituents R⁵, and

Ce-Ceo-aryl,

which is optionally substituted with one or more substituents R⁵; and

C3-C57-heteroaryl,

which is optionally substituted with one or more substituents R⁵;

and wherein apart from that the definitions in claim 1 apply.

7. Organic molecule according to one or more of claims 1 to 5, wherein the three second chemical moieties each at each occurrence, independently from another, comprise a structure of formula lie:

Formula lie wherein

R^b is at each occurrence independently from another selected from the group consisting of H, deuterium, N(R⁵)₂, OR⁵, Si(R⁵)₃, B(OR⁵)₂, 0S0₂R⁵, CF₃, CN, F, Br, I,

Ci-C₄o-alkyl,

which is optionally substituted with one or more substituents R⁵, and

Ci-C_4o-alkoxy,

which is optionally substituted with one or more substituents R⁵ and

Ci-C₄o-thioalkoxy, which is optionally substituted with one or more substituents R⁵ and

C₂-C4o-alkenyl,

which is optionally substituted with one or more substituents R⁵ and

C₂-C₄o-alkynyl,

which is optionally substituted with one or more substituents R⁵ and

Ce-Ceo-aryl,

which is optionally substituted with one or more substituents R⁵; and

C3-C57-heteroaryl,

which is optionally substituted with one or more substituents R⁵;

and wherein apart from that the definitions in claim 1 apply.

8. Organic molecule according to claim 6 or 7, wherein R^b is at each occurrence independently from another selected from the group consisting of

H,

Me, 'Pr, ^lBu, CN, CF₃,

Ph, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃ and Ph;

pyridinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃ and Ph;

pyrimidinyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃ and Ph;

carbazolyl, which is optionally substituted with one or more substituents independently from each other selected from the group consisting of Me, 'Pr, ^lBu, CN, CF₃ and Ph;

and

N(Ph)₂.

9. Method for preparing an organic molecule according to claims 1 to 8, comprising the step of providing a tri-R'-substituted 3-bromo-4-fluoro-benzonitrile as a reactant.

10. Use of an organic molecule according to one or more of claims 1 to 8 as a luminescent emitter and/or as a host material and/or as an electron transport material and/or as a hole injection material and/or as a hole blocking material in an optoelectronic device.

1 1 . Use according to claim 10, wherein the optoelectronic device is selected from the group consisting of:

• organic light-emitting diodes (OLEDS),

• light-emitting electrochemical cells,

• OLED-sensors, in particular non-hermetically shielded gas and vapor sensors,

• organic diodes,

• organic solar cells,

• organic transistors,

• organic field-effect transistors,

• organic lasers and

• down-conversion elements.

12. Composition, comprising:

(a) an organic molecule according to one or more of claims 1 to 8, in particular in the form of an emitter and/or a host, and

(b) an emitter and/or host material, which differs from the organic molecule, and

(c) optionally, a dye and/or a solvent.

13. Optoelectronic device, comprising an organic molecule according to one or more of claims 1 to 8 or a composition according to claim 12, in particular in the form of a device selected from the group consisting of organic light-emitting diode (OLED), light-emitting electrochemical cell, OLED-sensor, organic diode, organic solar cell, organic transistor, organic field-effect transistor, organic laser, and down-conversion element.

14. Optoelectronic device according to claim 13, comprising:

- a substrate,

- an anode, and

- a cathode, wherein the anode or the cathode are disposed on the substrate, and

- a light-emitting layer, which is arranged between the anode and the cathode and which comprises the organic molecule or the composition.

15. Method for producing an optoelectronic device, wherein an organic molecule according to any one of claims 1 to 8 or a composition according to claim 12 is used, in particular comprising processing of the organic molecule by a vacuum evaporation method or from a solution.