KR20230008602A - Compound for organic optoelectronic device, composition for organic optoelectronic device, organic optoelectronic device and display device - Google Patents

Abstract

The present invention relates to a compound for an organic optoelectronic device represented by a chemical formula 1, a composition for an organic optoelectronic device including the compound, an organic optoelectronic device, and a display device. The content of the chemical formula 1 is as defined in the specification. One embodiment provides the compound for the organic optoelectronic device capable of implementing a high-efficiency and long-life organic optoelectronic device.

Description

Compounds for organic optoelectronic devices, compositions for organic optoelectronic devices, organic optoelectronic devices and display devices

It relates to compounds for organic optoelectronic devices, compositions for organic optoelectronic devices, organic optoelectronic devices, and display devices.

An organic optoelectronic diode is a device capable of converting between electrical energy and light energy.

Organic optoelectronic devices can be largely divided into two types according to their operating principles. One is a photoelectric device that generates electrical energy as excitons formed by light energy are separated into electrons and holes and the electrons and holes are transferred to different electrodes, respectively. It is a light emitting device that generates light energy from

Examples of the organic optoelectronic device include an organic photoelectric device, an organic light emitting device, an organic solar cell, and an organic photo conductor drum.

Among them, organic light emitting diodes (OLEDs) have recently been attracting great attention due to an increase in demand for flat panel display devices. An organic light emitting device is a device that converts electrical energy into light, and the performance of the organic light emitting device is greatly affected by organic materials positioned between electrodes.

One embodiment provides a compound for an organic optoelectronic device capable of implementing a high-efficiency and long-life organic optoelectronic device.

Another embodiment provides a composition for an organic optoelectronic device including the compound.

Another embodiment provides an organic optoelectronic device including the compound.

Another embodiment provides a display device including the organic optoelectronic device.

According to one embodiment, a compound for an organic optoelectronic device represented by Chemical Formula 1 is provided.

[Formula 1]

In Formula 1,

X ¹ is O or S;

Z ¹ to Z ³ are each independently N or CR ^a ;

at least two of Z ¹ to Z ³ are N;

L ¹ to L ³ are each independently a single bond or a substituted or unsubstituted C6 to C30 arylene group;

Ar ¹ and Ar ² are each independently a substituted or unsubstituted C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,

R ^a and R ¹ to R ⁵ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, or a substituted or unsubstituted C6 to C20 aryl group;

R ⁶ and R ⁷ are each independently a substituted or unsubstituted C1 to C20 alkyl group or a substituted or unsubstituted C6 to C20 aryl group;

m1 and m2 are each independently an integer of 2 or 4;

m3 and m4 are each independently one of integers from 1 to 4;

n1 and n2 are each independently an integer of 0 or 1.

According to another embodiment, a composition for an organic optoelectronic device including a first compound and a second compound is provided.

The first compound is the aforementioned compound for an organic optoelectronic device, and the second compound may be represented by Chemical Formula 2 below.

[Formula 2]

In Formula 2,

X ² is O, S, NR ^b , CR ^c R ^d or SiR ^e R ^f ;

R ^b , R ^c , R ^d , R ^e , R ^f and R ⁸ are each independently hydrogen, deuterium, a substituted or unsubstituted amine group, a substituted or unsubstituted C1 to C30 alkyl group, or a substituted or unsubstituted C6 to C30 alkyl group. A C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,

m5 is an integer from 1 to 4;

Ring A is any one selected from the rings listed in Group II below,

[Group II]

In Group II,

* is the connection point,

X ³ is O, S, NR ^g , CR ^h R ⁱ or SiR ^j R ^k ;

R ^g , R ^h , R ⁱ , R ^j , R ^k , and R ⁹ to R ¹⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted amine group, a substituted or unsubstituted C1 to C30 alkyl group, or a substituted or unsubstituted A cyclic C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,

m6, m8, m11 and m13 are each independently an integer from 1 to 4,

m7, m9, m10 and m12 are each independently an integer of 1 or 2,

At least one of R ⁸ to R ¹⁶ is a group represented by the following formula (a),

[Formula a]

In the above formula (a),

L ⁴ to L ⁶ are each independently a single bond or a substituted or unsubstituted C6 to C30 arylene group;

Ar ³ and Ar ⁴ are each independently a substituted or unsubstituted amine group, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heterocyclic group;

* is a connection point.

According to another embodiment, comprising an anode and a cathode facing each other, at least one organic layer positioned between the anode and the cathode, wherein the organic layer includes the compound for an organic optoelectronic device or the composition for an organic optoelectronic device An organic optoelectronic device is provided.

According to another embodiment, a display device including the organic optoelectronic device is provided.

A high-efficiency, long-life organic optoelectronic device can be implemented.

1 is a cross-sectional view illustrating an organic light emitting device according to an exemplary embodiment.

Hereinafter, embodiments of the present invention will be described in detail. However, this is presented as an example, and the present invention is not limited thereby, and the present invention is only defined by the scope of the claims to be described later.

In this specification, unless otherwise defined, "substitution" means that at least one hydrogen in a substituent or compound is deuterium, a halogen group, a hydroxyl group, an amino group, a substituted or unsubstituted C1 to C30 amine group, a nitro group, a substituted or Unsubstituted C1 to C40 silyl group, C1 to C30 alkyl group, C1 to C10 alkylsilyl group, C6 to C30 arylsilyl group, C3 to C30 cycloalkyl group, C3 to C30 heterocycloalkyl group, C6 to C30 aryl group, C2 to C30 A heteroaryl group, a C1 to C20 alkoxy group, a C1 to C10 trifluoroalkyl group, a cyano group, or a combination thereof.

In one example of the present invention, "substitution" means that at least one hydrogen in a substituent or compound is deuterium, a C1 to C30 alkyl group, a C1 to C10 alkylsilyl group, a C6 to C30 arylsilyl group, a C3 to C30 cycloalkyl group, a C3 to C30 It means substituted with a heterocycloalkyl group, a C6 to C30 aryl group, a C2 to C30 heteroaryl group, or a cyano group. In addition, in a specific example of the present invention, "substitution" means that at least one hydrogen in a substituent or compound is substituted with deuterium, a C1 to C20 alkyl group, a C6 to C30 aryl group, or a cyano group. In addition, in a specific example of the present invention, "substitution" means that at least one hydrogen in a substituent or compound is substituted with deuterium, a C1 to C5 alkyl group, a C6 to C18 aryl group, or a cyano group. In addition, in a specific example of the present invention, "substitution" means that at least one hydrogen of a substituent or compound is substituted with deuterium, cyano group, methyl group, ethyl group, propyl group, butyl group, phenyl group, biphenyl group, terphenyl group or naphthyl group. means it has been

In this specification, “unsubstituted” means that a hydrogen atom remains as a hydrogen atom without being substituted with another substituent.

In this specification, “hydrogen substitution (-H) may include “deuterium substitution (-D) or” tritium substitution (-T).

In this specification, unless otherwise defined, "hetero" means containing 1 to 3 heteroatoms selected from the group consisting of N, O, S, P and Si in one functional group, and the rest being carbon. .

In the present specification, "aryl group" is a general concept of a group having one or more hydrocarbon aromatic moieties, and all elements of the hydrocarbon aromatic moiety have p-orbitals, and these p-orbitals are conjugated Forming a form, for example, including a phenyl group, a naphthyl group, etc., including a form in which two or more hydrocarbon aromatic moieties are connected through a sigma bond, for example, a biphenyl group, a terphenyl group, a quaterphenyl group, etc., and two or more hydrocarbon aromatic moieties may include a non-aromatic fused ring in which they are directly or indirectly fused, such as a fluorenyl group and the like.

Aryl groups include monocyclic, polycyclic or fused-ring polycyclic (ie, rings having split adjacent pairs of carbon atoms) functional groups.

In the present specification, a "heterocyclic group" is a higher concept including a heteroaryl group, and in a ring compound such as an aryl group, a cycloalkyl group, a fused ring thereof, or a combination thereof, N, O, It means containing at least one heteroatom selected from the group consisting of S, P and Si. When the heterocyclic group is a fused ring, the entire heterocyclic group or each ring may include one or more heteroatoms.

For example, "heteroaryl group" means containing at least one heteroatom selected from the group consisting of N, O, S, P, and Si in the aryl group. Two or more heteroaryl groups may be directly connected through a sigma bond, or if the heteroaryl group includes two or more rings, the two or more rings may be fused to each other. When the heteroaryl group is a fused ring, each ring may contain 1 to 3 hetero atoms.

More specifically, the substituted or unsubstituted C6 to C30 aryl group is a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, a substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted phenanthrenyl group. An unsubstituted naphthacenyl group, a substituted or unsubstituted pyrenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted p-terphenyl group, a substituted or unsubstituted m-terphenyl group, a substituted or unsubstituted o- Terphenyl group, substituted or unsubstituted chrysenyl group, substituted or unsubstituted triphenylene group, substituted or unsubstituted perylenyl group, substituted or unsubstituted fluorenyl group, substituted or unsubstituted indenyl group, substituted or unsubstituted It may be a cyclic furanyl group, or a combination thereof, but is not limited thereto.

More specifically, the substituted or unsubstituted C2 to C30 heterocyclic group is a substituted or unsubstituted thiophenyl group, a substituted or unsubstituted pyrrolyl group, a substituted or unsubstituted pyrazolyl group, a substituted or unsubstituted imidazolyl group, Substituted or unsubstituted triazolyl group, substituted or unsubstituted oxazolyl group, substituted or unsubstituted thiazolyl group, substituted or unsubstituted oxadiazolyl group, substituted or unsubstituted thiazolyl group, substituted or unsubstituted A substituted or unsubstituted pyrimidinyl group, a substituted or unsubstituted pyrazinyl group, a substituted or unsubstituted triazinyl group, a substituted or unsubstituted benzofuranyl group, a substituted or unsubstituted benzothiophenyl group, A substituted or unsubstituted benzimidazolyl group, a substituted or unsubstituted indolyl group, a substituted or unsubstituted quinolinyl group, a substituted or unsubstituted isoquinolinyl group, a substituted or unsubstituted quinazolinyl group, a substituted or unsubstituted quinoxalinyl group, substituted or unsubstituted naphthyridinyl group, substituted or unsubstituted benzoxazinyl group, substituted or unsubstituted benzthiazinyl group, substituted or unsubstituted acridinyl group, substituted or unsubstituted phenazine Dial, substituted or unsubstituted phenothiazinyl group, substituted or unsubstituted phenoxazinyl group, substituted or unsubstituted carbazolyl group, substituted or unsubstituted dibenzofuranyl group, substituted or unsubstituted dibenzothiophenyl group , a substituted or unsubstituted benzonaphthofuranyl group, a substituted or unsubstituted benzonaphthothiophenyl group, a substituted or unsubstituted dibenzosilolyl group, or a combination thereof, but is not limited thereto.

In the present specification, the hole characteristic refers to a characteristic that can form holes by donating electrons when an electric field is applied, and has conduction characteristics along the HOMO level, so that holes formed at the anode are injected into the light emitting layer, the light emitting layer It means a property that facilitates the movement of holes formed in the anode to the anode and in the light emitting layer.

In addition, electronic properties refer to the characteristics of receiving electrons when an electric field is applied, and has conductivity along the LUMO level, so that electrons formed in the cathode are injected into the light emitting layer, electrons formed in the light emitting layer move to the cathode, and in the light emitting layer A property that facilitates movement.

Hereinafter, a compound for an organic optoelectronic device according to an embodiment will be described.

A compound for an organic optoelectronic device according to an embodiment is represented by Formula 1 below.

[Formula 1]

In Formula 1,

X ¹ is O or S;

Z ¹ to Z ³ are each independently N or CR ^a ;

at least two of Z ¹ to Z ³ are N;

L ¹ to L ³ are each independently a single bond or a substituted or unsubstituted C6 to C30 arylene group;

Ar ¹ and Ar ² are each independently a substituted or unsubstituted C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,

R ^a and R ¹ to R ⁵ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, or a substituted or unsubstituted C6 to C20 aryl group;

R ⁶ and R ⁷ are each independently a substituted or unsubstituted C1 to C20 alkyl group or a substituted or unsubstituted C6 to C20 aryl group;

m1 and m2 are each independently an integer of 2 or 4;

m3 and m4 are each independently one of integers from 1 to 4;

n1 and n2 are each independently an integer of 0 or 1.

The compound represented by Chemical Formula 1 has a structure in which pyrimidine or triazine is substituted for a benzene ring located in the middle of a backbone in which benzosylol is additionally fused at positions 3 and 4 of dibenzofuran (or dibenzothiophene).

Since the polyfused ring formed by additional fusion of benzosilol has a twisted structure rather than a perfectly flat state, crystallinity is reduced and Tg is improved. In addition, due to the decrease in crystallinity, processability during deposition may be improved.

In addition, as pyrimidine or triazine is substituted, high electron mobility may be obtained, thereby reducing driving voltage.

In particular, as the pyrimidine or triazine is substituted for the benzene ring located in the middle, the LUMO phore expands smoothly from side to side, and stability to electrons is excellent, so that the lifespan of the device can be improved.

In addition, as it contains a fused ring containing silicon, it has excellent heat resistance compared to a carbon fused ring.

Chemical Formula 1 may be represented by the following Chemical Formula 1A or Chemical Formula 1B depending on the specific substitution position of the triazine.

[Formula 1A]

[Formula 1B]

In Formula 1A and Formula 1B,

X ¹ , Z ¹ to Z ³ , L ¹ to L ³ , Ar ¹ , Ar ² , R ¹ to R ⁷ , m1 to m4, n1 and n2 are as described above.

In addition, depending on whether the end of the fused ring is additionally fused, it may be represented by any one of Formulas 1-1 to 1-7 below.

[Formula 1-1] [Formula 1-2]

[Formula 1-3] [Formula 1-4]

[Formula 1-5] [Formula 1-6]

[Formula 1-7]

In Formula 1-1 to Formula 1-7,

X ¹ , Z ¹ to Z ³ , L ¹ to L ³ , Ar ¹ , Ar ² , R ¹ to R ⁷ , and m1 to m4 are as described above.

In one embodiment, L ¹ to L ³ may each independently be a single bond, a substituted or unsubstituted phenylene group, or a substituted or unsubstituted naphthylene group.

In a specific embodiment, L ¹ is a single bond, and L ² and L ³ may each independently be a single bond or a substituted or unsubstituted phenylene group.

In one embodiment, Ar ¹ and Ar ² are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted phenanthrenyl group, or a substituted or unsubstituted biphenyl group. It may be a substituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, or a substituted or unsubstituted dibenzosilolyl group.

In a specific embodiment, Ar ¹ and Ar ² are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, or It may be a substituted or unsubstituted dibenzothiophenyl group.

As a more specific example, *-L ² -Ar ¹ and *-L ³ -Ar ² may each independently be selected from substituents listed in Group I below.

[Group I]

In Group I,

D is deuterium;

m14 is an integer from 0 to 5;

m15 is an integer from 0 to 4;

m16 is an integer from 0 to 7;

m17 is an integer from 0 to 3;

m18 is an integer from 0 to 6;

m19 is an integer from 0 to 2;

* is a connection point.

In the above definitions of m14 to m19, 0 means that all hydrogen atoms remain as hydrogen atoms without being substituted with deuterium, that is, “unsubstituted”.

In one embodiment, R ¹ to R ⁵ may each independently be hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C12 aryl group.

In a specific embodiment, R ¹ to R ⁵ may each independently represent hydrogen or deuterium.

In one embodiment, R ⁶ and R ⁷ may each independently be a substituted or unsubstituted C1 to C10 alkyl group or a substituted or unsubstituted C6 to C12 aryl group.

In a specific embodiment, R ⁶ and R ⁷ may each independently be a substituted or unsubstituted methyl group or a substituted or unsubstituted phenyl group.

For example, the compound for an organic optoelectronic device represented by Chemical Formula 1 may be one selected from compounds listed in Group 1 below, but is not limited thereto.

[Group 1]

[1] [2] [3] [4]

[5] [6] [7] [8]

[9] [10] [11] [12]

[13] [14] [15] [16]

[17] [18] [19] [20]

[21] [22] [23] [24]

[25] [26] [27] [28]

[29] [30] [31] [32]

[33] [34] [35] [36]

[37] [38] [39] [40]

[41] [42] [43] [44]

[45] [46] [47] [48]

[49] [50] [51] [52]

[53] [54] [55] [56]

[57] [58] [59] [60]

[61] [62] [63] [64]

[65] [66] [67] [68]

[69] [70] [71] [72]

[73] [74] [75] [76]

[77] [78] [79] [80]

[81] [82] [83] [84]

[85] [86] [87] [88]

[89] [90] [91] [92]

[93] [94] [95] [96]

[97] [98] [99] [100]

[101] [102] [103] [104]

[105] [106] [107] [108]

[109] [110] [111] [112]

[113] [114] [115] [116]

[117] [118] [119] [120]

[121] [122] [123] [124]

[125] [126] [127] [128]

[129] [130] [131] [132]

[133] [134] [135] [136]

[137] [138] [139] [140]

[141] [142] [143] [144]

[145] [146] [147] [148]

[149] [150] [151] [152]

[153] [154] [155] [156]

[157] [158] [159] [160]

[161] [162] [163] [164]

A composition for an organic optoelectronic device according to another embodiment includes a first compound and a second compound, wherein the first compound is the aforementioned compound for an organic optoelectronic device, and the second compound may be represented by Formula 2 below. there is.

[Formula 2]

In Formula 2,

X ² is O, S, NR ^b , CR ^c R ^d or SiR ^e R ^f ;

R ^b , R ^c , R ^d , R ^e , R ^f and R ⁸ are each independently hydrogen, deuterium, a substituted or unsubstituted amine group, a substituted or unsubstituted C1 to C30 alkyl group, or a substituted or unsubstituted C6 to C30 alkyl group. A C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,

m5 is an integer from 1 to 4;

Ring A is any one selected from the rings listed in Group II below,

[Group II]

In Group II,

* is the connection point,

X ³ is O, S, NR ^g , CR ^h R ⁱ or SiR ^j R ^k ;

R ^g , R ^h , R ⁱ , R ^j , R ^k , and R ⁹ to R ¹⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted amine group, a substituted or unsubstituted C1 to C30 alkyl group, or a substituted or unsubstituted A cyclic C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,

m6, m8, m11 and m13 are each independently an integer from 1 to 4,

m7, m9, m10 and m12 are each independently an integer of 1 or 2,

At least one of R ⁸ to R ¹⁶ is a group represented by the following formula (a),

[Formula a]

In the above formula (a),

L ⁴ to L ⁶ are each independently a single bond or a substituted or unsubstituted C6 to C30 arylene group;

Ar ³ and Ar ⁴ are each independently a substituted or unsubstituted amine group, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heterocyclic group;

* is a connection point.

The second compound may have a structure in which amine is substituted for carbazole/fused carbazole/fused dibenzofuran/fused dibenzothiophene/fused dibenzosilol, and depending on the type and fusion position of the additional benzene ring, for example, the following formula It can be represented by any one of 2-I to Formula 2-IX.

[Formula 2-Ⅰ] [Formula 2-Ⅱ]

[Formula 2-Ⅲ] [Formula 2-IV]

[Formula 2-V] [Formula 2-VI]

[Formula 2-VII] [Formula 2-VIII]

[Formula 2-Ⅸ]

In Formula 2-I to Formula 2-IX,

X ² , X ³ , R ⁸ to R ¹¹ , R ¹⁵ , R ¹⁶ , m5 to m8, m12 and m13 are as described above.

In addition, according to the substitution direction of the amine group, the second compound may be represented by any one of the following Formulas 2-IA to 2-IXA, Formula 2-IIB to Formula 2-IXB, and Formula 2-IIC to Formula 2-IXC there is.

[Formula 2-ⅠA] [Formula 2-ⅡA]

[Formula 2-IIIA] [Formula 2-IVA]

[Formula 2-ⅤA] [Formula 2-ⅥA]

[Formula 2-VIIA] [Formula 2-VIIIA]

[Formula 2-IXA]

In Formula 2-IA to Formula 2-IXA,

X ² , X ³ , L ⁴ to L ⁶ , Ar ³ , Ar ⁴ , R ⁸ to R ¹¹ , R ¹⁵ , R ¹⁶ , m6 to m8, m12 and m13 are as described above;

m5' is one of integers from 1 to 3.

[Formula 2-IIB] [Formula 2-IIIB]

[Formula 2-ⅣB] [Formula 2-ⅤB]

[Formula 2-VIB] [Formula 2-VIIB]

[Formula 2-ⅧB] [Formula 2-ⅨB]

In Formula 2-IIB to Formula 2-IXB,

X ² , X ³ , L ⁴ to L ⁶ , R ⁸ , R ¹⁰ , R ¹¹ , R ¹⁵ , R ¹⁶ , Ar ³ , Ar ⁴ , m5, m7 and m12 are as described above;

m8' and m13' are each independently one of integers from 1 to 3.

[Formula 2-IIC] [Formula 2-IIIC]

[Formula 2-ⅣC] [Formula 2-ⅤC]

[Formula 2-VIC] [Formula 2-VIIC]

[Formula 2-ⅧC] [Formula 2-ⅨC]

In Formula 2-IIC to Formula 2-IXC,

X ² , X ³ , L ⁴ to L ⁶ , Ar ³ , Ar ⁴ , R ⁸ , R ¹⁰ , R ¹¹ , R ¹⁵ , R ¹⁶ , m5, m8 and m13 are as described above.

For example, R ⁸ to R ¹⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted amine group, a substituted or unsubstituted C1 to C30 alkyl group, or a substituted or unsubstituted C6 to C30 aryl group.

The second compound according to an embodiment may be represented by Chemical Formula 2-IVB or Chemical Formula 2-VIIIB.

For example, X ² in Formula 2-IVB may be NR ^b .

For example, X ² in Formula 2-VIIIB may be O or S, and X ³ may be CR ^h R ⁱ or SiR ^j R ^k .

Here, R ^b , R ^h , R ⁱ , R ^j and R ^k may each independently be a substituted or unsubstituted C1 to C10 alkyl group or a substituted or unsubstituted C6 to C20 aryl group.

The second compound according to a specific embodiment may be represented by Chemical Formula 2-IVB-2 or Chemical Formula 2-VIIIB-2.

[Formula 2-ⅣB-2] [Formula 2-VIIIB-2]

In Formula 2-IVB-2 and Formula 2-VIIIB-2,

L ⁴ to L ⁶ are each independently a single bond or a substituted or unsubstituted phenylene group;

Ar ³ and Ar ⁴ are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, or a substituted or unsubstituted naphthyl group,

X ² is NR ^b , O or S;

X ³ is CR ^h R ⁱ or SiR ^j R ^k ;

R ^b , R ^h , R ⁱ , R ^j and R ^k are each independently a substituted or unsubstituted C1 to C10 alkyl group or a substituted or unsubstituted C6 to C20 aryl group,

R ⁸ , R ¹⁰ , R ¹¹ , R ¹⁵ and R ¹⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group or a substituted or unsubstituted C6 to C30 aryl group,

m5 is an integer from 1 to 4;

m7 and m12 are each independently an integer of 1 or 2;

m8' and m13' are each independently one of integers from 1 to 3.

For example, L ⁴ to L ⁶ may each independently be a single bond, a substituted or unsubstituted phenylene group, or a substituted or unsubstituted biphenylene group.

For example, Ar ³ and Ar ⁴ are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted naphthyl group, or a substituted or unsubstituted phenanthyl group. A substituted or unsubstituted triphenylene group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, It may be a substituted or unsubstituted benzofurano fluorenyl group or a substituted or unsubstituted benzothiophene fluorenyl group.

For example, the second compound may be one selected from compounds listed in Group 2 below, but is not limited thereto.

[Group 2]

2-31 2-32 2-33 2-34

2-35 2-36 2-37 2-38

2-39 2-40

2-41 2-42 2-43 2-44

2-45 2-46 2-47 2-48

2-49 2-50

2-51 2-52

2-53 2-54 2-55 2-56 2-57

2-58 2-59 2-60

2-61 2-62 2-63 2-64

2-65 2-66 2-67 2-68

2-69 2-70 2-71 2-72

2-73 2-74 2-75 2-76

2-77 2-78 2-79 2-80

2-81 2-82 2-83

2-84 2-85 2-86

2-87 2-88 2-89

2-90 2-91 2-92 2-93

2-94 2-95 2-96 2-97

2-98 2-99 2-100 2-101

2-102 2-103 2-104 2-105

2-106 2-107 2-108 2-109

2-110 2-111 2-112 2-113

2-114 2-115 2-116 2-117

2-118 2-119 2-120 2-121

2-122 2-123 2-124 2-125

2-126 2-127 2-128 2-129

2-130 2-131 2-132 2-133

2-134 2-135 2-136 2-137

2-138 2-139 2-140 2-141

2-142 2-143 2-144 2-145

2-146 2-147 2-148 2-149

2-150 2-151 2-152 2-153

2-154 2-155 2-156 2-157

2-158 2-159 2-160 2-161

2-162 2-163 2-164 2-165

2-166 2-167 2-168 2-169

2-170 2-171 2-172 2-173

2-174 2-175 2-176 2-177

2-178 2-179 2-180 2-181

2-182 2-183 2-184 2-185

2-186 2-187 2-188 2-189

2-190 2-191 2-192 2-193

2-194 2-195 2-196 2-197

2-198 2-199 2-200 2-201

2-202 2-203 2-204 2-205

2-206 2-207 2-208 2-209

The first compound and the second compound may be included in a weight ratio of, for example, 1:99 to 99:1. By being included within the above range, efficiency and lifespan can be improved by implementing bipolar characteristics by setting an appropriate weight ratio using the electron transport capability of the first compound and the hole transport capability of the second compound. Within the above range, for example, it may be included in a weight ratio of about 10:90 to 90:10, about 20:80 to 80:20, for example, about 20:80 to about 70:30, about 20:80 to about 60:40, And it may be included in a weight ratio of about 30:70 to about 60:40. As a specific example, it may be included in a weight ratio of 40:60, 50:50, or 60:40.

In addition to the first compound and the second compound described above, one or more compounds may be further included.

The aforementioned compound for an organic optoelectronic device or composition for an organic optoelectronic device may be a composition that further includes a dopant.

The dopant may be, for example, a phosphorescent dopant, for example, a red, green or blue phosphorescent dopant, and may be, for example, a red or green phosphorescent dopant.

A dopant is a compound or composition for an organic optoelectronic device that is mixed in a small amount to cause light emission. In general, a material such as a metal complex that emits light by multiple excitation that excites a triplet state or higher is used. can The dopant may be, for example, an inorganic, organic, or organic-inorganic compound, and may include one type or two or more types.

An example of the dopant may include a phosphorescent dopant, and examples of the phosphorescent dopant include Ir, Pt, Os, Ti, Zr, Hf, Eu, Tb, Tm, Fe, Co, Ni, Ru, Rh, Pd, or a combination thereof. Organometallic compounds containing As the phosphorescent dopant, for example, a compound represented by Chemical Formula Z may be used, but is not limited thereto.

[Formula Z]

L ⁷ MX ⁴

In Formula Z, M is a metal, L ⁷ and X ⁴ are the same as or different from each other and are ligands that form a complex with M.

M may be, for example, Ir, Pt, Os, Ti, Zr, Hf, Eu, Tb, Tm, Fe, Co, Ni, Ru, Rh, Pd or combinations thereof, and L ⁷ and X ⁴ may be, for example, bi It may be a dentate ligand.

Examples of the ligand represented by L ⁷ and X ⁴ may be selected from the formulas listed in Group A below, but are not limited thereto.

[Group A]

In the group A,

R ³⁰⁰ to R ³⁰² are each independently hydrogen, deuterium, a C1 to C30 alkyl group with or without halogen substitution, a C6 to C30 aryl group with or without C1 to C30 alkyl substitution, or halogen;

R ³⁰³ to R ³²⁴ are each independently hydrogen, deuterium, halogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C3 to C30 cycloalkyl group, or a substituted Or an unsubstituted C2 to C30 alkenyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C1 to C30 heteroaryl group, a substituted or unsubstituted C1 to C30 amino group, a substituted or unsubstituted C6 to C30 arylamino group, SF ₅ , a trialkylsilyl group having a substituted or unsubstituted C1 to C30 alkyl group, a dialkylarylsilyl group having a substituted or unsubstituted C1 to C30 alkyl group and a C6 to C30 aryl group, or It is a triarylsilyl group having a substituted or unsubstituted C6 to C30 aryl group.

For example, a dopant represented by Chemical Formula V below may be included.

[Formula V]

In Formula V,

R ¹⁰¹ to R ¹¹⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C20 aryl group, or -SiR ¹³² R ¹³³ R ¹³⁴ ;

Wherein R ¹³² to R ¹³⁴ are each independently a C1 to C6 alkyl group;

At least one of R ¹⁰¹ to R ¹¹⁶ is a functional group represented by Formula V-1 below;

L ¹⁰⁰ is a bidentate ligand of a monovalent anion, and is a ligand that coordinates with iridium through an unshared electron pair of a carbon or heteroatom,

m15 and m16 are independently any one of integers from 0 to 3, m15 + m16 is any one of integers from 1 to 3,

[Formula V-1]

In Formula V-1,

R ¹³⁵ to R ¹³⁹ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C20 aryl group, or -SiR ¹³² R ¹³³ R ¹³⁴ ;

Wherein R ¹³² to R ¹³⁴ are each independently a C1 to C6 alkyl group;

* means a part connected to a carbon atom.

For example, a dopant represented by Chemical Formula Z-1 may be included.

[Formula Z-1]

In the above formula Z-1, rings A, B, C, and D each independently represent a 5- or 6-membered carbocyclic or heterocyclic ring;

R ^A , R ^B , R ^C , and R ^D each independently represent mono-, di-, tri-, or tetra-substituted, or unsubstituted;

L ^B , L ^C , and L ^D are each a direct bond, BR, NR, PR, O, S, Se, C=O, S=O, SO ₂ , CRR', SiRR', GeRR', and combinations thereof independently selected from the group consisting of;

When nA is 1, L ^E is a group consisting of a direct bond, BR, NR, PR, O, S, Se, C=O, S=O, SO ₂ , CRR', SiRR', GeRR', and combinations thereof is selected from; When nA is 0, L ^E is not present;

R ^A , R ^B , R ^C , R ^D , R , and R' are each hydrogen, deuterium, halogen, alkyl group, cycloalkyl group, heteroalkyl group, arylalkyl group, alkoxy group, aryloxy group, amino group, silyl group, alkenyl group , Cycloalkenyl group, heteroalkenyl group, alkynyl group, aryl group, heteroaryl group, acyl group, carbonyl group, carboxylic acid group, ester group, nitrile group, isonitrile group, sulfanyl group, sulfinyl group, sulfonyl group, phosphino group independently selected from the group consisting of, and combinations thereof; any adjacent R ^A , R ^B , R ^C , R ^D , R , and R' are optionally linked to form a ring; X ^B , X ^C , X ^D , and X ^E are each independently selected from the group consisting of carbon and nitrogen; Q ¹ , Q ² , Q ³ , and Q ⁴ each represent an oxygen or a direct bond.

A dopant according to an embodiment may be a platinum complex, and may be represented by Chemical Formula VI below.

[Formula VI]

In Formula VI,

X ¹⁰⁰ is selected from O, S and NR ¹³¹ ;

R ¹¹⁷ to R ¹³¹ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C20 aryl group, or - SiR ¹³² R ¹³³ R ¹³⁴ ;

Wherein R ¹³² to R ¹³⁴ are each independently a C1 to C6 alkyl group;

At least one of R ¹¹⁷ to R ¹³¹ is -SiR ¹³² R ¹³³ R ¹³⁴ or a tert-butyl group.

Hereinafter, an organic optoelectronic device to which the above-described compound for an organic optoelectronic device or composition for an organic optoelectronic device is applied will be described.

The organic optoelectronic device is not particularly limited as long as it is a device capable of converting electrical energy and light energy, and examples thereof include an organic photoelectric device, an organic light emitting device, an organic solar cell, and an organic photoreceptor drum.

Here, an organic light emitting device, which is an example of an organic optoelectronic device, will be described with reference to drawings.

1 is a cross-sectional view showing an organic light emitting device according to an exemplary embodiment.

Referring to FIG. 1 , an organic light emitting device 100 according to an embodiment includes an anode 120 and a cathode 110 facing each other, and an organic layer 105 positioned between the anode 120 and the cathode 110. include

The anode 120 may be made of, for example, a conductor having a high work function so as to smoothly inject holes, and may be made of, for example, a metal, a metal oxide, and/or a conductive polymer. The anode 120 may be formed of, for example, a metal such as nickel, platinum, vanadium, chromium, copper, zinc, or gold or an alloy thereof; metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO); combinations of metals and oxides such as ZnO and Al or SnO ₂ and Sb; conductive polymers such as poly(3-methylthiophene), poly(3,4-(ethylene-1,2-dioxy)thiophene) (polyehtylenedioxythiophene: PEDOT), polypyrrole, and polyaniline; It is not.

The cathode 110 may be made of, for example, a conductor having a low work function so as to facilitate electron injection, and may be made of, for example, metal, metal oxide, and/or conductive polymer. The negative electrode 110 may be formed of, for example, metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin, lead, cesium, barium, or alloys thereof; Multi-layer structure materials such as LiF/Al, LiO ₂ /Al, LiF/Ca, and BaF ₂ /Ca may be mentioned, but are not limited thereto.

The organic layer 105 may include the above-described compound for an organic optoelectronic device or composition for an organic optoelectronic device.

The organic layer 105 includes the light emitting layer 130, and the light emitting layer 130 may include the above-described compound for an organic optoelectronic device or composition for an organic optoelectronic device.

The composition for an organic optoelectronic device further comprising a dopant may be, for example, a red light emitting composition.

The light emitting layer 130 may include, for example, the first compound and the second compound described above as a phosphorescent host, respectively.

The organic layer may further include a charge transport region in addition to the light emitting layer.

The charge transport region may be, for example, the hole transport region 140 .

The hole transport region 140 may further increase hole injection and/or hole mobility between the anode 120 and the light emitting layer 130 and block electrons. Specifically, the hole transport region 140 may include a hole transport layer between the anode 120 and the light emitting layer 130, and a hole transport auxiliary layer between the light emitting layer 130 and the hole transport layer. At least one of the listed compounds may be included in at least one of the hole transport layer and the hole transport auxiliary layer.

[Group B]

In addition to the above compounds, known compounds described in US5061569A, JP1993-009471A, WO1995-009147A1, JP1995-126615A, JP1998-095973A and similar structures may be used for the hole transport region 140.

Also, the charge transport region may be, for example, the electron transport region 150 .

The electron transport region 150 may further increase electron injection and/or electron mobility between the cathode 110 and the light emitting layer 130 and block holes.

Specifically, the electron transport region 150 may include an electron transport layer between the cathode 110 and the light emitting layer 130, and an electron transport auxiliary layer between the light emitting layer 130 and the electron transport layer. At least one of the listed compounds may be included in at least one of the electron transport layer and the electron transport auxiliary layer.

[Group C]

One embodiment may be an organic light emitting device including a light emitting layer as an organic layer.

Another embodiment may be an organic light emitting device including a light emitting layer and a hole transport region as an organic layer.

Another embodiment may be an organic light emitting device including an emission layer and an electron transport region as an organic layer.

As shown in FIG. 1 , an organic light emitting device according to an exemplary embodiment of the present invention may include a hole transport region 140 and an electron transport region 150 in addition to the emission layer 130 as the organic layer 105 .

Meanwhile, the organic light emitting device may further include an electron injection layer (not shown), a hole injection layer (not shown), and the like in addition to the light emitting layer as the organic layer described above.

In the organic light emitting device 100, after forming an anode or a cathode on a substrate, an organic layer is formed by a dry film method such as evaporation, sputtering, plasma plating, or ion plating, and then a cathode or cathode thereon. It can be manufactured by forming an anode.

The organic light emitting device described above may be applied to an organic light emitting display device.

The above-described implementation will be described in more detail through the following examples. However, the following examples are for illustrative purposes only and do not limit the scope of rights.

Hereinafter, the starting materials and reactants used in Examples and Synthesis Examples were purchased from Sigma-Aldrich, TCI, Tokyo chemical industry or P&H tech, or synthesized through known methods, unless otherwise specified.

(Preparation of compounds for organic optoelectronic devices)

A compound presented as a more specific example of the compound of the present invention was synthesized through the following steps.

Synthesis Example 1: Synthesis of Compound 64

[Scheme 1]

Step 1: Synthesis of Intermediate 64-1

After dissolving 4-bromo-1-chlorodibenzofuran (50.0 g, 178 mmol) and triisopropyl borate (40.1 g, 213 mmol) in 1 L of anhydrous THF, the mixture was stirred at -78°C. After 30 minutes, n-butyllithium 2.5M solution (85.2 mL, 213 mmol) was slowly added dropwise and stirred for 12 hours. When the reaction is complete, a small amount of dilute hydrochloric acid is added and stirred for 1 hour. After extracting twice with a mixed solvent of distilled water and dichloromethane to separate the organic layer, the organic solvent in the organic layer is concentrated using a rotary evaporator. The concentrated organic layer was slurry stirred/purified with n -hexane to obtain 34.6 g (79.0%) of intermediate 64-1.

Step 2: Synthesis of Intermediate 64-2

Intermediate 64-1 (34.6 g, 140 mmol), 1-bromo-2-iodobenzene (41.7 g, 147 mmol), Pd(PPh ₃ ) ₄ (8.1 g, 7 mmol) and K ₂ CO ₃ (58.2 g, 421 mmol) in 700 mL of a mixed solvent of tetrahydrofuran: distilled water = 2: 1 and stirred under reflux at 80 ° C for 12 hours. Upon completion of the reaction, 41.2 g (82.1%) of intermediate 64-2 was obtained by recrystallization with a mixed solvent of dichloromethane and n-hexane.

Step 3: Synthesis of Intermediate 64-3

Intermediate 64-2 (41.2 g, 115 mmol) was dissolved in 600 mL of anhydrous THF and stirred at -78°C. After 30 minutes, n-butyllithium 2.5M solution (55.2 mL, 138 mmol) was slowly added dropwise. After 30 minutes, dichlorodimethylsilane (12.0 g, 127 mmol) was slowly added dropwise and stirred for 12 hours. After the reaction was completed, the organic layer was separated by extraction twice with a mixed solvent of ethyl acetate and distilled water, and the organic layer was purified by silica gel column chromatography to obtain 23.1 g (59.4%) of intermediate 64-3.

Step 4: Synthesis of Intermediate 64-4

Intermediate 64-3 (23.1 g, 69 mmol) and tris(triphenylphosphine)rhodium(I) chloride (1.3 g, 1 mmol) were dissolved in 300 mL of 1,4-dioxane and stirred under reflux at 110 °C for 12 hours. After the reaction was completed, 15.5 g (67.5%) of intermediate 64-4 was obtained by column chromatography purification with a dichloromethane: n-hexane mixed solvent.

Step 5: Synthesis of Intermediate 64-5

Intermediate 64-4 (15.5 g, 46 mmol), bis(pinacolato)diboron (15.3 g, 60 mmol), potassium acetate (13.6 g, 139 mmol), tricyclohexylphosphine (2.6 g, 9 mmol) and [1,1'- bis(diphenylphosphino)ferrocene]-dichloropalladium(II) (1.9 g, 2 mmol) was added to 250 mL of N , N -dimethylformamide, followed by reflux stirring at 150°C for 12 hours. When the reaction is complete, the solution is poured into an excess of DIW to form a precipitate. The precipitate is filtered, boiled and dissolved in toluene, and filtered through silica gel. The filtered solution was recrystallized to obtain 17.7 g (89.7%) of Intermediate 64-5.

Step 6: Synthesis of Compound 64

Intermediate 64-5 and 2-chloro-4-(dibenzo[b,d]furan-1-yl)-6-phenyl-1,3,5-triazine as starting materials, Synthesis Example 1, Intermediate 64-2, 2 Compound 64 was synthesized by synthesizing/purifying in the same manner as in the step. LC/MS calculated for: C41H27N3O2Si Exact Mass: 621.19 found for 622.30 [M+H]

Synthesis Example 2: Synthesis of Compound 84

[Scheme 2]

Intermediate 64-5 and 2-([1,1'-biphenyl]-4-yl)-4-chloro-6-phenyl-1,3,5-triazine were used as starting materials, and the same method as in Synthesis Example 1, step 2 Compound 84 was synthesized by synthesis/purification. LC/MS calculated for: C41H29N3OSi Exact Mass: 607.21 found for 608.27 [M+H]

Synthesis Example 3: Synthesis of Compound 85

[Scheme 3]

Intermediate 64-5 and 2-([1,1'-biphenyl]-3-yl)-4-chloro-6-phenyl-1,3,5-triazine are used as starting materials, and the same method as in Synthesis Example 1 step 2 Compound 85 was synthesized by synthesis/purification. LC/MS calculated for: C41H29N3OSi Exact Mass: 607.21 found for 608.43 [M+H]

Synthesis Example 4: Synthesis of Compound 134

[Scheme 4]

Intermediate 134-5 was synthesized through the same synthesis method as in Steps 1 to 5 of Synthesis Example 1, except that 2,3-dibromonaphthalene was added instead of 1-bromo-2-iodobenzene in Step 2 of Synthesis Example 1 to react. Compound 134 was synthesized by synthesizing/purifying the intermediate 134-5 and 2-chloro-4,6-diphenyl-1,3,5-triazine as starting materials in the same manner as in step 2 of Synthesis Example 1. LC/MS calculated for: C39H27N3OSi Exact Mass: 581.19 found for 582.20 [M+H]

Synthesis Example 5: Synthesis of Compound 142

[Scheme 5]

Step 1: Synthesis of Intermediate 142-1

Dissolve 7-chloronaphtho[1,2-b]benzofuran (50.0 g, 198 mmol) in 1 L of anhydrous THF and stir at -78°C. After 30 minutes, n-butyllithium 2.5M solution (95.0 mL, 237 mmol) was slowly added thereto, and the mixture was further stirred at room temperature for 8 hours. After 8 hours, the mixture was cooled to -78°C again, and triisopropyl borate (44.7 g, 237 mmol) was slowly added thereto and stirred for 12 hours. When the reaction is complete, a small amount of dilute hydrochloric acid is added and stirred for 1 hour. After extracting twice with a mixed solvent of distilled water and dichloromethane to separate the organic layer, the organic solvent in the organic layer is concentrated using a rotary evaporator. The concentrated organic layer was slurry stirred/purified with n -hexane to obtain 36.2 g (74.3%) of intermediate 142-1.

Step 2: Synthesis of Compound 142

In step 2 of Synthesis Example 1, Intermediate 142-5 was synthesized through the same synthesis method as in Steps 1 to 5 of Synthesis Example 1, except that Intermediate 142-1 was added instead of Intermediate 64-1 and reacted. Compound 142 was synthesized by synthesizing/purifying -5 and 2-chloro-4,6-diphenyl-1,3,5-triazine as starting materials in the same manner as in Step 2 of Synthesis Example 1. LC/MS calculated for: C39H27N3OSi Exact Mass: 581.19 found for 582.10 [M+H]

Comparative Synthesis Example 1: Synthesis of Compound C-1

[Scheme 6]

Step 1: Synthesis of Intermediate C-1-1

Intermediate C-1-1 was synthesized by synthesizing/purifying 4-bromo-1-chlorodibenzofuran and (2-(methoxycarbonyl)phenyl)boronic acid as starting materials in the same manner as in Step 2 of Synthesis Example 1.

Step 2: Synthesis of Intermediate C-1-2

Intermediate C-1-1 (85.4 g, 254 mmol) was dissolved in 500 mL of anhydrous THF, and methylmagnesium bromide solution (211.8 mL, 634 mmol) was slowly added dropwise at -78°C. When the reaction is complete after 12 hours, the solution is slowly poured into ice water. After extracting twice with ethyl acetate and distilled water, filter with silica gel. All organic layers were evaporated and dried without further purification to obtain 72.6 g (85.0%) of intermediate C-1-2.

Step 3: Synthesis of Intermediate C-1-3

Intermediate C-1-2 (72.6 g, 216 mmol) was dissolved in 400 mL of MC, and boron trifluoride etherate (29.3 mL, 237 mmol) was slowly added dropwise at 0°C. When the reaction is complete after 12 hours, the solution is slowly poured into distilled water. After extracting twice with dichloromethane and distilled water, filter with silica gel. The organic layer was evaporated and recrystallized from toluene to obtain 37.3 g (54.3%) of intermediate C-1-3.

Step 4: Synthesis of Intermediate C-1-4

Compound intermediate C-1-4 was synthesized by synthesizing/purifying Intermediate C-1-3 as a starting material in the same manner as in Synthesis Example 1, Step 5.

Step 5: Synthesis of Compound C-1

Compound C-1 was synthesized by synthesizing/purifying intermediate C-1-4 and 2-chloro-4,6-diphenylpyrimidine as starting materials in the same manner as in Step 2 of Synthesis Example 1. LC/MS calculated for: C37H26N2O Exact Mass: 514.20 found for 515.43 [M+H]

Comparative Synthesis Example 2: Synthesis of Compound C-2

[Scheme 7]

Step 1: Synthesis of Intermediate C-2-1

Intermediate C-1-4 and 1-bromo-4-chlorobenzene were synthesized/purified in the same manner as in Step 2 of Synthesis Example 1 using 1-bromo-4-chlorobenzene as starting materials to synthesize Intermediate C-2-1.

Step 2: Synthesis of Intermediate C-2-2

Intermediate C-2-2 was synthesized by synthesizing/purifying Intermediate C-2-1 as a starting material in the same manner as in Synthesis Example 1, Step 5.

Step 3: Synthesis of Compound C-2

Compound C-2 was synthesized by synthesizing/purifying intermediate C-2-2 and 2-chloro-4,6-diphenyltriazine as starting materials in the same manner as in step 2 of Synthesis Example 1. LC/MS calculated for: C42H29N3O Exact Mass: 591.23 found for 592.40 [M+H]

Comparative Synthesis Example 3: Synthesis of Compound C-3

[Scheme 8]

Step 1: Synthesis of Intermediate C-3-1

Intermediate C-1-1 and phenylmagnesium bromide were synthesized/purified in the same manner as in Step 2 of Comparative Synthesis Example 1 using starting materials to synthesize Intermediate C-3-1.

Step 2: Synthesis of Intermediate C-3-2

Intermediate C-3-2 was synthesized by synthesizing/purifying Intermediate C-3-1 as a starting material in the same manner as in Step 3 of Comparative Synthesis Example 1.

Step 3: Synthesis of Intermediate C-3-3

Intermediate C-3-3 was synthesized by synthesizing/purifying Intermediate C-3-2 as a starting material in the same manner as in Step 4 of Comparative Synthesis Example 1.

Step 4: Synthesis of Compound C-3

Compound C-3 was synthesized by synthesizing/purifying intermediate C-3-3 and 2-chloro-4,6-diphenyltriazine as starting materials in the same manner as in step 2 of Synthesis Example 1. LC/MS calculated for: C46H29N3O Exact Mass: 639.23 found for 640.33 [M+H]

Comparative Synthesis Example 4: Synthesis of Compound C-4

[Scheme 9]

Intermediate C-4 through the same synthesis method as in Steps 1 to 4 of Comparative Synthesis Example 1, except that 4-bromo-1-chlorodibenzothiophene was added instead of 4-bromo-1-chlorodibenzofuran in Step 1 of Comparative Synthesis Example 1. -4 was synthesized, and compound C-4 was synthesized by synthesizing/purifying the intermediate C-4-4 and 2-chloro-4,6-diphenylpyrimidine as starting materials in the same manner as in step 2 of Synthesis Example 1. LC/MS calculated for: C37H26N2S Exact Mass: 530.18 found for 531.22 [M+H]

Comparative Synthesis Example 5: Synthesis of Compound C-5

[Scheme 10]

Intermediate C-5-2 through the same synthesis method as in Steps 1 and 2 of Comparative Synthesis Example 2, except that Intermediate C-4-4 was added instead of Intermediate C-1-4 in Step 1 of Comparative Synthesis Example 2 and reacted. was synthesized, and compound C-5 was synthesized by synthesizing/purifying the intermediate C-5-2 and 2-chloro-4,6-diphenyltriazine as starting materials in the same manner as in step 2 of Synthesis Example 1. LC/MS calculated for: C42H29N3S Exact Mass: 607.21 found for 608.47 [M+H]

Comparative Synthesis Example 6: Synthesis of Compound C-6

[Scheme 11]

Step 1: Synthesis of Intermediate C-6-1

1-chloro-4-fluorobenzene (103.7 g, 794 mmol), 2,6-dibromophenol (50.0 g, 199 mmol) and K ₂ CO ₃ (82.3 g, 596 mmol) were dissolved in 1 L of NMP and stirred under reflux at 180 °C. do. When the reaction is complete after 12 hours, the solution is slowly poured into distilled water. After extracting twice with dichloromethane and distilled water, filter with silica gel. The organic layer was evaporated and slurry purified with methyl alcohol to obtain 62.7 g (87.2%) of intermediate C-6-1.

Step 2: Synthesis of Intermediate C-6-2

Intermediate C-6-1 (62.7 g, 173 mmol), Pd(OAc) ₂ (1.9 g, 9 mmol), PCy ₃ HBF ₄ (10.0 g, 26 mmol) and K ₂ CO ₃ (47.8 g, 346 mmol) was dissolved in 800 mL of DMAc and stirred under reflux at 180 °C. When the reaction is complete after 12 hours, the solution is slowly poured into distilled water. After extracting twice with dichloromethane and distilled water, filter with silica gel. The organic layer was evaporated and recrystallized from a mixture of dichloromethane and n-hexane to obtain 20.0 g (41.1%) of intermediate C-6-2.

Step 3: Synthesis of Intermediate C-6-3

Intermediate C-6-2 was synthesized/purified in the same manner as in Synthesis Example 1, Step 1, using Intermediate C-6-2 as a starting material to synthesize Intermediate C-6-3.

Step 4: Synthesis of Intermediate C-6-4

Intermediate C-6-3 was synthesized/purified in the same manner as in the second step of Synthesis Example 1 using the starting material to synthesize Intermediate C-6-4.

Step 5: Synthesis of Intermediate C-6-5

Intermediate C-6-4 was synthesized/purified in the same manner as in Synthesis Example 1, Step 3, using Intermediate C-6-4 as a starting material to synthesize Intermediate C-6-5.

Step 6: Synthesis of Intermediate C-6-6

Intermediate C-6-6 was synthesized by synthesizing/purifying Intermediate C-6-5 as a starting material in the same manner as in Step 4 of Synthesis Example 1.

Step 7: Synthesis of Intermediate C-6-7

Intermediate C-6-6 was synthesized/purified in the same manner as in Step 5 of Synthesis Example 1 using the starting material to synthesize Intermediate C-6-7.

Step 8: Synthesis of Compound C-6

Compound C-6 was synthesized by synthesizing/purifying intermediate C-6-7 and 2-chloro-4,6-diphenyltriazine as starting materials in the same manner as in step 2 of Synthesis Example 1. LC/MS calculated for: C35H25N3OSi Exact Mass: 531.18 found for 532.22 [M+H]

Synthesis Example 6: Synthesis of Compound A-84

[Scheme 12]

Step 1: Synthesis of Intermediate 2-1a

Phenylhydrazinehydrochloride (70.0 g, 484.1 mmol) and 7-bromo-3,4-dihydro-2H-naphthalen-1-one (108.9 g, 484.1 mmol) were put in a round bottom flask and dissolved in ethanol (1200 ml). After slowly adding 60 mL of hydrochloric acid dropwise at room temperature, the mixture was stirred at 90°C for 12 hours. When the reaction is complete, the solvent is removed under reduced pressure and then extracted with an excess of EA. The organic solvent was removed under reduced pressure, stirred in a small amount of methanol, and filtered to obtain 95.2 g (66%) of intermediate 2-1a.

Step 2: Synthesis of Intermediate 2-1b

Intermediate 2-1a (95.2g, 319.3 mmol) and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (108.7g, 478.9 mmol) were put in a round bottom flask and dissolved in toluene (600ml). Stir at 80° C. for 12 hours. After the reaction was completed, the reaction solvent was removed and 41.3 g (44%) of intermediate 2-1b was obtained by column chromatography.

Step 3: Synthesis of Intermediate 2-1c

Intermediate 2-1b (41.3g, 139.0 mmol), iodobenzene (199.2g, 976.0 mmol), CuI (5.31g, 28.0 mmol), K ₂ CO ₃ (28.9g, 209.0 mmol), and 1,10-phenanthroline (5.03 g, 28.0 mmol) into a round bottom flask and dissolved in DMF (500ml). Stir at 180° C. for 12 hours. After the reaction is completed, the reaction solvent is removed under reduced pressure, dissolved in dichloromethane, and filtered through silica gel. After concentration in dichloromethane, recrystallization from hexane yielded 39.0 g (75%) of intermediate 2-1c.

Step 4: Synthesis of Compound A-84

5.0 g (13.46 mmol) of intermediate 2-1c and 4.41 g (13.46 mmol) of intermediate amine 2-1d, 1.94 g (20.19 mmol) of sodium t-butoxide, and Tri-tert-butylphosphine ( butylphosphine) 0.54 g (1.35 mmol) was dissolved in 100 ml of toluene, and Pd (dba) ₂ 0.37 g (0.4 mmol) was added thereto, followed by reflux stirring for 12 hours under a nitrogen atmosphere. After completion of the reaction, after extraction with toluene and distilled water, the organic layer was dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The product was purified by silica gel column chromatography with n-hexane/dichloromethane (2:1 volume ratio) to obtain 6.4 g of compound A-84 (yield: 82.0%).

Synthesis Example 7: Synthesis of Compound 2-92

[Scheme 13]

Step 1: Synthesis of Intermediate 2-92a

It was synthesized by referring to patent KR10-1423173 B1.

Step 2: Synthesis of compound 2-92

5.0 g (16.93 mmol) of intermediate 2-92a and 5.4 g (16.93 mmol) of amine intermediate 2-92b, 2.44 g (25.39 mmol) of sodium t-butoxide, and Tri-tert-butylphosphine ( butylphosphine) 0.68 g (1.69 mmol) was dissolved in toluene 100 ml, and Pd (dba) ₂ 0.47 g (0.51 mmol) was added, followed by reflux stirring for 12 hours under a nitrogen atmosphere. After completion of the reaction, after extraction with toluene and distilled water, the organic layer was dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The product was purified by silica gel column chromatography using n-hexane/dichloromethane (2:1 volume ratio) to obtain 8.2 g of the target compound 2-92 (yield: 84.0%).

(Manufacture of organic light emitting device)

Example 1

A glass substrate coated with ITO (Indium tin oxide) to a thickness of 1,500 Å was washed with distilled water. After the distilled water cleaning was completed, the substrate was ultrasonically cleaned with a solvent such as isopropyl alcohol, acetone, or methanol, dried, transferred to a plasma cleaner, cleaned for 10 minutes using oxygen plasma, and then transferred to a vacuum evaporator. Using the prepared ITO transparent electrode as an anode, compound A doped with 3% NDP-9 (commercially available from Novaled) was vacuum deposited on the ITO substrate to form a hole injection layer with a thickness of 100 Å, and the hole injection layer Compound A was deposited thereon to a thickness of 1300 Å to form a hole transport layer. Compound B was deposited to a thickness of 700 Å on top of the hole transport layer to form a hole transport auxiliary layer. Compound 64 obtained in Synthesis Example 1 was used as a host on the hole transport auxiliary layer, and [Ir(piq) ₂ acac] was doped at 2 wt% as a dopant to form a light emitting layer having a thickness of 400 Å by vacuum deposition. Subsequently, compound C was deposited on the light emitting layer to a thickness of 50 Å to form an electron transport auxiliary layer, and compound D and LiQ were simultaneously vacuum deposited at a weight ratio of 1: 1 to form an electron transport layer with a thickness of 300 Å. An organic light emitting device was fabricated by forming a cathode by sequentially vacuum depositing 15 Å of Liq and 1,200 Å of Al on the electron transport layer.

The organic light emitting device has a structure having 5 organic thin film layers, and is specifically as follows.

ITO / Compound A (3% NDP-9 doping, 100Å) / Compound A (1300Å) / Compound B (700Å) / EML [Compound 64: [Ir(piq) ₂ acac] = 98: 2 (w/w)] (400Å) / Compound C (50Å) / Compound D: Liq (300Å) / LiQ (15Å) / Al (1200Å).

Compound A: N-(biphenyl-4-yl)-9,9-dimethyl-N-(4-(9-phenyl-9H-carbazol-3-yl)phenyl)-9H-fluoren-2-amine

Compound B: N,N-di([1,1'-biphenyl]-4-yl)-7,7-dimethyl-7H-fluoreno[4,3-b]benzofuran-10-amine

Compound C: 2-(3-(3-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)phenyl)-4,6-diphenyl-1,3,5-triazine

Compound D: 8-(4-(4,6-di(naphthalen-2-yl)-1,3,5-triazin-2-yl)phenyl)quinoline

Examples 2 to 5 and Comparative Examples 1 to 6

As shown in Table 1 below, devices of Examples 2 to 5 and Comparative Examples 1 to 6 were fabricated in the same manner as in Example 1, except that the host was changed.

Examples 6 to 15 and Comparative Examples 7 to 12

As shown in Table 2 below, the host was changed, and the first host and the second host were mixed at a weight ratio of 5:5, and Examples 6 to 15 and Comparative Examples 7 to 12 were prepared in the same manner as in Example 1. device was made.

evaluation

The luminous efficiency and lifetime characteristics of the organic light emitting devices according to Examples 1 to 15 and Comparative Examples 1 to 12 were evaluated. The specific measurement method is as follows, and the results are shown in Tables 1 and 2.

(1) Measurement of change in current density according to voltage change

With respect to the manufactured organic light emitting device, while increasing the voltage from 0V to 10V, a current value flowing through the unit device was measured using a current-voltmeter (Keithley 2400), and the result was obtained by dividing the measured current value by the area.

(2) Measurement of luminance change according to voltage change

For the manufactured organic light emitting device, while increasing the voltage from 0V to 10V, the luminance at that time was measured using a luminance meter (Minolta Cs-1000A), and the result was obtained.

(3) Measurement of luminous efficiency

Current efficiency (cd/A) of the same current density (10 mA/cm ² ) was calculated using the luminance, current density, and voltage measured from (1) and (2) above.

Relative values based on the luminous efficiency of Comparative Example 1 and Comparative Example 7 were calculated and shown in Tables 1 and 2 below.

(4) life measurement

For the organic light emitting device manufactured, the devices of Examples 1 to 15 and Comparative Examples 1 to 12 were emitted at an initial luminance (cd/m ² ) of 6,000 cd/m ² using the Polaronics lifetime measurement system, and time elapsed. By measuring the decrease in luminance according to , the time point when the luminance decreased to 95% compared to the initial luminance was measured as the T95 lifespan.

Relative values based on the T95 lifespan of Comparative Example 1 and Comparative Example 7 were calculated and shown in Tables 1 and 2 below.

(5) Driving voltage measurement

The result was obtained by measuring the driving voltage of each device at 15 mA/cm ² using a current-voltmeter (Keithley 2400).

Relative values based on the driving voltages of Comparative Example 1 and Comparative Example 7 were calculated and shown in Tables 1 and 2 below.

division sole host Driving voltage (%) efficiency (%) Example 1 compound 64 88 115 Example 2 compound 84 88 115 Example 3 compound 85 90 113 Example 4 compound 134 90 113 Example 5 compound 142 90 115 Comparative Example 1 compound C-1 100 100 Comparative Example 2 compound C-2 92 103 Comparative Example 3 compound C-3 93 110 Comparative Example 4 compound C-4 101 101 Comparative Example 5 compound C-5 93 103 Comparative Example 6 compound C-6 97 103

division host T95 lifetime (%) Driving voltage (%) efficiency (%) first host 2nd host Example 6 compound 64 Compound A-84 350 85 120 Example 7 compound 64 compound 2-92 250 92 130 Example 8 compound 84 Compound A-84 350 85 115 Example 9 compound 84 compound 2-92 260 91 130 Example 10 compound 85 Compound A-84 200 90 112 Example 11 compound 85 compound 2-92 180 94 115 Example 12 compound 134 Compound A-84 300 89 112 Example 13 compound 134 compound 2-92 250 94 115 Example 14 compound 142 Compound A-84 300 88 120 Example 15 compound 142 compound 2-92 220 93 125 Comparative Example 7 compound C-1 Compound A-84 100 100 100 Comparative Example 8 compound C-2 compound 2-92 120 102 103 Comparative Example 9 compound C-3 Compound A-84 150 99 99 Comparative Example 10 compound C-4 compound 2-92 50 105 102 Comparative Example 11 compound C-5 Compound A-84 70 98 100 Comparative Example 12 compound C-6 compound 2-92 50 105 105

Referring to Tables 1 and 2, it can be seen that when the compound according to the present invention is used as a mixed host in combination with a single host and a second host, the driving voltage, efficiency and lifespan are significantly improved compared to those using the comparative compound.

Although the embodiments have been described in detail, the scope of the present invention is not limited thereto, and various modifications and improvements of those skilled in the art using the basic concepts of the present invention defined in the following claims also fall within the scope of the present invention. will be.

100: organic light emitting element
105 organic layer
110: cathode
120: anode
130: light emitting layer
140: hole transport region
150: electron transport area

Claims (15)

A compound for an organic optoelectronic device represented by Formula 1:
[Formula 1]

In Formula 1,
X ¹ is O or S;
Z ¹ to Z ³ are each independently N or CR ^a ;
at least two of Z ¹ to Z ³ are N;
L ¹ to L ³ are each independently a single bond or a substituted or unsubstituted C6 to C30 arylene group;
Ar ¹ and Ar ² are each independently a substituted or unsubstituted C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,
R ^a and R ¹ to R ⁵ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, or a substituted or unsubstituted C6 to C20 aryl group;
R ⁶ and R ⁷ are each independently a substituted or unsubstituted C1 to C20 alkyl group or a substituted or unsubstituted C6 to C20 aryl group;
m1 and m2 are each independently an integer of 2 or 4;
m3 and m4 are each independently one of integers from 1 to 4;
n1 and n2 are each independently an integer of 0 or 1. According to claim 1,
Formula 1 is a compound for an organic optoelectronic device, which is represented by Formula 1A or Formula 1B:
[Formula 1A]

[Formula 1B]

In Formula 1A and Formula 1B,
X ¹ , Z ¹ to Z ³ , L ¹ to L ³ , Ar ¹ , Ar ² , R ¹ to R ⁷ , m1 to m4, n1 and n2 are defined as in claim 1. According to claim 1,
Chemical Formula 1 is a compound for an organic optoelectronic device, which is represented by any one of the following Chemical Formulas 1-1 to 1-7:
[Formula 1-1] [Formula 1-2]

[Formula 1-3] [Formula 1-4]

[Formula 1-5] [Formula 1-6]

[Formula 1-7]

In Formula 1-1 to Formula 1-7,
X ¹ , Z ¹ to Z ³ , L ¹ to L ³ , Ar ¹ , Ar ² , R ¹ to R ⁷ , and m1 to m4 are defined as in claim 1. According to claim 1,
Wherein L ¹ to L ³ are each independently a single bond, a substituted or unsubstituted phenylene group, or a substituted or unsubstituted naphthylene group, a compound for an organic optoelectronic device. According to claim 1,
Ar ¹ and Ar ² are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted phenanthrenyl group, or a substituted or unsubstituted carbazolyl group. , A substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, or a substituted or unsubstituted dibenzosilolyl group, a compound for an organic optoelectronic device. According to claim 1,
Wherein *-L ² -Ar ¹ and *-L ³ -Ar ² are each independently one selected from substituents listed in Group I, Compound for Organic Optoelectronic Device:
[Group I]

In Group I,
D is deuterium;
m14 is an integer from 0 to 5;
m15 is an integer from 0 to 4;
m16 is an integer from 0 to 7;
m17 is an integer from 0 to 3;
m18 is an integer from 0 to 6;
m19 is an integer from 0 to 2;
* is a connection point. According to claim 1
A compound for an organic optoelectronic device selected from the compounds listed in Group 1 below:
[Group 1]
[1] [2] [3] [4]

[5] [6] [7] [8]

[9] [10] [11] [12]

[13] [14] [15] [16]

[17] [18] [19] [20]

[21] [22] [23] [24]

[25] [26] [27] [28]

[29] [30] [31] [32]

[33] [34] [35] [36]

[37] [38] [39] [40]

[41] [42] [43] [44]

[45] [46] [47] [48]

[49] [50] [51] [52]

[53] [54] [55] [56]

[57] [58] [59] [60]

[61] [62] [63] [64]

[65] [66] [67] [68]

[69] [70] [71] [72]

[73] [74] [75] [76]

[77] [78] [79] [80]

[81] [82] [83] [84]

[85] [86] [87] [88]

[89] [90] [91] [92]

[93] [94] [95] [96]

[97] [98] [99] [100]

[101] [102] [103] [104]

[105] [106] [107] [108]

[109] [110] [111] [112]

[113] [114] [115] [116]

[117] [118] [119] [120]

[121] [122] [123] [124]

[125] [126] [127] [128]

[129] [130] [131] [132]

[133] [134] [135] [136]

[137] [138] [139] [140]

[141] [142] [143] [144]

[145] [146] [147] [148]

[149] [150] [151] [152]

[153] [154] [155] [156]

[157] [158] [159] [160]

[161] [162] [163] [164]

. Including a first compound, and a second compound,
The first compound is a compound for an organic optoelectronic device according to claim 1,
The second compound is a compound for an organic optoelectronic device represented by Formula 2, a composition for an organic optoelectronic device:
[Formula 2]

In Formula 2,
X ² is O, S, NR ^b , CR ^c R ^d or SiR ^e R ^f ;
R ^b , R ^c , R ^d , R ^e , R ^f and R ⁸ are each independently hydrogen, deuterium, a substituted or unsubstituted amine group, a substituted or unsubstituted C1 to C30 alkyl group, or a substituted or unsubstituted C6 to C30 alkyl group. A C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,
m5 is an integer from 1 to 4;
Ring A is any one selected from the rings listed in Group II below,
[Group II]

In Group II,
* is the connection point,
X ³ is O, S, NR ^g , CR ^h R ⁱ or SiR ^j R ^k ;
R ^g , R ^h , R ⁱ , R ^j , R ^k , and R ⁹ to R ¹⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted amine group, a substituted or unsubstituted C1 to C30 alkyl group, or a substituted or unsubstituted A cyclic C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,
m6, m8, m11 and m13 are each independently an integer of 1 to 4,
m7, m9, m10 and m12 are each independently an integer of 1 or 2;
At least one of R ⁸ to R ¹⁶ is a group represented by the following formula (a),
[Formula a]

In the above formula (a),
L ⁴ to L ⁶ are each independently a single bond or a substituted or unsubstituted C6 to C30 arylene group;
Ar ³ and Ar ⁴ are each independently a substituted or unsubstituted amine group, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heterocyclic group;
* is a connection point. According to claim 8,
Chemical Formula 2 is a composition for an organic optoelectronic device represented by any one of the following Chemical Formulas 2-I to 2-IX:
[Formula 2-Ⅰ] [Formula 2-Ⅱ]

[Formula 2-Ⅲ] [Formula 2-IV]

[Formula 2-V] [Formula 2-VI]

[Formula 2-VII] [Formula 2-VIII]

[Formula 2-Ⅸ]

In Formula 2-I to Formula 2-IX,
X ² , X ³ , R ⁸ to R ¹¹ , R ¹⁵ , R ¹⁶ , m5 to m8, m12 and m13 are the same as in claim 8. According to claim 9,
The second compound is represented by any one of the following Formulas 2-IA to 2-IXA, Formula 2-IIB to Formula 2-IXB, and Formula 2-IIC to Formula 2-IXC Composition for an organic optoelectronic device:
[Formula 2-ⅠA] [Formula 2-ⅡA]

[Formula 2-IIIA] [Formula 2-IVA]

[Formula 2-ⅤA] [Formula 2-ⅥA]

[Formula 2-VIIA] [Formula 2-VIIIA]

[Formula 2-IXA]

In Formula 2-IA to Formula 2-IXA,
X ² , X ³ , L ⁴ to L ⁶ , Ar ³ , Ar ⁴ , R ⁸ to R ¹¹ , R ¹⁵ , R ¹⁶ , m6 to m8, m12 and m13 are as defined in claim 9,
m5' is an integer from 1 to 3;
[Formula 2-IIB] [Formula 2-IIIB]

[Formula 2-ⅣB] [Formula 2-ⅤB]

[Formula 2-VIB] [Formula 2-VIIB]

[Formula 2-ⅧB] [Formula 2-ⅨB]

In Formula 2-IIB to Formula 2-IXB,
X ² , X ³ , L ⁴ to L ⁶ , R ⁸ , R ¹⁰ , R ¹¹ , R ¹⁵ , R ¹⁶ , Ar ³ , Ar ⁴ , m5, m7 and m12 are as defined in claim 9,
m8' and m13' are each independently an integer from 1 to 3;
[Formula 2-IIC] [Formula 2-IIIC]

[Formula 2-ⅣC] [Formula 2-ⅤC]

[Formula 2-VIC] [Formula 2-VIIC]

[Formula 2-ⅧC] [Formula 2-ⅨC]

In Formula 2-IIC to Formula 2-IXC,
X ² , X ³ , L ⁴ to L ⁶ , Ar ³ , Ar ⁴ , R ⁸ , R ¹⁰ , R ¹¹ , R ¹⁵ , R ¹⁶ , m5, m8 and m13 are as defined in claim 9. According to claim 8,
The R ⁸ to R ¹⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted amine group, a substituted or unsubstituted C1 to C30 alkyl group, or a substituted or unsubstituted C6 to C30 aryl group, an organic optoelectronic device composition. According to claim 9,
Wherein the second compound is represented by Formula 2-IVB-2 or Formula 2-VIIIB-2, a composition for an organic optoelectronic device:
[Formula 2-ⅣB-2] [Formula 2-VIIIB-2]

In Formula 2-IVB-2 and Formula 2-VIIIB-2,
L ⁴ to L ⁶ are each independently a single bond or a substituted or unsubstituted phenylene group;
Ar ³ and Ar ⁴ are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, or a substituted or unsubstituted naphthyl group,
X ² is NR ^b , O or S;
X ³ is CR ^h R ⁱ or SiR ^j R ^k ;
R ^b , R ^h , R ⁱ , R ^j and R ^k are each independently a substituted or unsubstituted C1 to C10 alkyl group or a substituted or unsubstituted C6 to C20 aryl group,
R ⁸ , R ¹⁰ , R ¹¹ , R ¹⁵ and R ¹⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group or a substituted or unsubstituted C6 to C30 aryl group,
m5 is an integer from 1 to 4;
m7 and m12 are each independently an integer of 1 or 2,
m8' and m13' are each independently an integer of 1 to 3; anode and cathode facing each other,
At least one organic layer positioned between the anode and the cathode,
The organic layer includes a light emitting layer,
The light-emitting layer may include a compound for an organic optoelectronic device according to any one of claims 1 to 7; Or an organic optoelectronic device comprising the composition for an organic optoelectronic device according to any one of claims 8 to 12. According to claim 13,
The compound for an organic optoelectronic device or the composition for an organic optoelectronic device is included as a host of the light emitting layer. A display device comprising the organic optoelectronic device according to claim 13 .

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