KR20230066253A - 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 chemical formula 1, a composition for an organic optoelectronic device containing the same, an organic optoelectronic device, and a display device. The contents of chemical formula 1 are as defined in the present specification. The present invention can implement high-efficiency and long-lifespan organic optoelectronic devices.

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,

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 and L ² are each independently a single bond, a substituted or unsubstituted C6 to C30 arylene group or a substituted or unsubstituted C2 to C30 heterocyclic 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,

Ar ³ is a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted pyrimidinyl group, a substituted or unsubstituted triazinyl group, a substituted or unsubstituted dibenzofuranyl group, A substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted benzonaphthofuranyl group, or a substituted or unsubstituted benzonaphthothiophenyl group,

R ^a , R ¹ and R ² are each independently hydrogen, deuterium, 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 one of integers from 1 to 3,

When m2 is 2 or more, each R ² is independently present or adjacent R ² are fused to form a ring.

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 ¹ 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 ³ 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 or a substituted or unsubstituted C2 to C30 heterocyclic group,

m3 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 ² 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 ⁴ to 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 A cyclic C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,

m4, m6, and m8 are each independently an integer of 1 to 4;

m5 and m7 are each independently an integer of 1 or 2;

At least one of R ³ to R ⁸ is a group represented by the following formula (a),

[Formula a]

In the above formula (a),

L ³ to L ⁵ are each independently a single bond or a substituted or unsubstituted C6 to C30 arylene group;

Ar ⁴ and Ar ⁵ 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- A terphenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted perylenyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted indenyl group, or any of these It may be a combination, but is not limited thereto.

More specifically, the substituted or unsubstituted C2 to C30 heterocyclic group is a substituted or unsubstituted furanyl group, a substituted or unsubstituted thiophenyl group, a substituted or unsubstituted pyrrolyl group, a substituted or unsubstituted pyrazolyl group, or a substituted or unsubstituted pyrazolyl group. Or an unsubstituted imidazolyl group, a substituted or unsubstituted triazolyl group, a substituted or unsubstituted oxazolyl group, a substituted or unsubstituted thiazolyl group, a substituted or unsubstituted oxadiazolyl group, a substituted or unsubstituted Thiadiazolyl group, substituted or unsubstituted pyridyl group, substituted or unsubstituted pyrimidinyl group, substituted or unsubstituted pyrazinyl group, substituted or unsubstituted triazinyl group, substituted or unsubstituted benzofuranyl group, substituted Or an 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, substituted or unsubstituted quinoxalinyl group, substituted or unsubstituted naphthyridinyl group, substituted or unsubstituted benzoxazinyl group, substituted or unsubstituted benzothiazinyl group, substituted or unsubstituted acridinyl group , A substituted or unsubstituted phenazinyl group, a substituted or unsubstituted phenothiazinyl group, a substituted or unsubstituted phenoxazinyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or It may be an 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. does not

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,

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 and L ² are each independently a single bond, a substituted or unsubstituted C6 to C30 arylene group or a substituted or unsubstituted C2 to C30 heterocyclic 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,

Ar ³ is a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted pyrimidinyl group, a substituted or unsubstituted triazinyl group, a substituted or unsubstituted dibenzofuranyl group, A substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted benzonaphthofuranyl group, or a substituted or unsubstituted benzonaphthothiophenyl group,

R ^a , R ¹ and R ² are each independently hydrogen, deuterium, 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 one of integers from 1 to 3,

When m2 is 2 or more, each R ² is independently present or adjacent R ² are fused to form a ring.

The compound represented by Formula 1 has a structure in which a nitrogen-containing 6-membered ring and Ar ³ are substituted at positions 1 and 5, respectively, through a naphthalene derivative.

By substituting at the 1st and 5th positions of the naphthalene derivative, the bond angle can be maximized and the stability between the host-host and host-dopant can be improved by giving a steric twist effect, thereby inducing a decrease in the half height width, which is applied The efficiency and lifetime of the device can be improved.

Ar ³ is a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted benzonaphthofuranyl group, a substituted or unsubstituted dibenzofuranyl group, It may be a cyclic benzonaphthothiophenyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted pyrimidinyl group, or a substituted or unsubstituted triazinyl group. In particular, when the Ar ³ is a C6 to C30 aryl group substituted with a cyano group, the cyano group has a strong electron-withdrawing property and acts as an excellent electron acceptor, so the Ar ³ is a substituted or unsubstituted pyridyl group, a substituted or unsubstituted pyridyl group, As in the case of an unsubstituted pyrimidinyl group or a substituted or unsubstituted triazinyl group, the overall LUMO area is enlarged and LUMO/HOMO are effectively separated according to the structure, so efficiency and lifespan improvement effects can be expected.

In addition, the cyano group has little structural change between the non-luminescence-inactivated state and the excited state, so that PL efficiency can be improved.

In Formula 1, when m1 is 2 or more, each R ¹ may be the same as or different from each other.

In Formula 1, when m2 is 2 or more, each R ² may be the same as or different from each other.

Formula 1 may be represented by Formula 1-1 or Formula 1-2 below.

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

In Formula 1-1 and Formula 1-2,

Z ¹ to Z ³ , L ¹ , L ² , Ar ¹ to Ar ³ , R ¹ and m1 are as described above;

R ^2a , R ^2b , R ^2c , R ^2d , R ^2e , R ^2f and R ^2g are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, or a substituted or unsubstituted C6 to C20 aryl group. .

Ar ¹ and Ar ² 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, a substituted or unsubstituted anthracenyl group, A substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted benzophenanthrenyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted group substituted dibenzosilolyl group, substituted or unsubstituted dibenzofuranyl group, substituted or unsubstituted dibenzothiophenyl group, substituted or unsubstituted carbazolyl group, substituted or unsubstituted benzonaphthofuranyl group, substituted or unsubstituted Cyclized benzonaphthothiophenyl group, substituted or unsubstituted dinaphthofuranyl group, substituted or unsubstituted dinaphthothiophenyl group, substituted or unsubstituted fused dibenzofuranyl group, substituted or unsubstituted fused dibenzothiophene Dial, substituted or unsubstituted benzocarbazinyl group, substituted or unsubstituted phenoxazinyl group, substituted or unsubstituted thiophenoxazinyl group, substituted or unsubstituted benzophenoxazinyl group, substituted or unsubstituted benzothiophene Noxazinyl group, substituted or unsubstituted 10-phenyl-10H-spiro[acridine-9,9'-fluorenyl group], substituted or unsubstituted 10H -spiro[acridine-9,9 '-fluorenyl group], or a substituted or unsubstituted spiro[fluorene-9,9'-xanthenyl group].

For example, Ar ¹ and Ar ² 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, a substituted or unsubstituted triphenylene group, or a substituted or unsubstituted triphenylene group. Or an unsubstituted fluorenyl group, a substituted or unsubstituted dibenzosilolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, or a substituted or unsubstituted carbazolyl group. there is.

For example, 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 dibenzosilolyl group, or a substituted or unsubstituted dibenzofuranyl group. , or a substituted or unsubstituted dibenzothiophenyl group.

For example, Ar ³ is a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, or a substituted or unsubstituted terphenyl group. substituted or unsubstituted phenanthrenyl group, substituted or unsubstituted fluorenyl group, substituted or unsubstituted dibenzofuranyl group, substituted or unsubstituted dibenzothiophenyl group, substituted or unsubstituted benzonaphthofuranyl group, substituted or unsubstituted may be a substituted or unsubstituted benzonaphthothiophenyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted pyrimidinyl group, or a substituted or unsubstituted triazinyl group.

As a specific example, Ar ³ is a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl 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. It may be an unsubstituted fluorenyl group, a substituted or unsubstituted dibenzofuranyl group, or a substituted or unsubstituted benzonaphthofuranyl group.

For example, Ar ³ may be a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, a substituted or unsubstituted phenanthrenyl group, or a substituted or unsubstituted dibenzofuranyl group. there is.

When Ar ³ is substituted, the substituent may be a cyano group.

For example, L ¹ and L ² are each independently a single bond, a substituted or unsubstituted phenylene group, a substituted or unsubstituted biphenylene group, a substituted or unsubstituted naphthylene group, or a substituted or unsubstituted phenanthrenylene group. , It may be a substituted or unsubstituted dibenzofuranylene group or a substituted or unsubstituted dibenzothiophenylene group.

For example, each of L ¹ and L ² may be a single bond.

In one embodiment, *-L ¹ -Ar ¹ and *-L ² -Ar ² may each independently be selected from substituents listed in Group I below.

[Group I]

In Group I above, * is a connection point.

The substituent may be unsubstituted or substituted with at least one additional substituent.

The additional substituent may be deuterium, a C1 to C10 alkyl group, or a C6 to C12 aryl group.

In one embodiment, R ^a , R ¹ and R ² 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, Ar ¹ and Ar ² are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted dibenzofuranyl group, or a substituted or unsubstituted dibenzothiophenyl group, and Ar ³ is a substituted or an unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted dibenzofuranyl group, or a substituted or unsubstituted dibenzothiophenyl group, wherein L ¹ and L ² may each be a single bond.

In a specific embodiment, R ¹ and R ² are each independently hydrogen, a substituted or unsubstituted methyl group, or a substituted or unsubstituted phenyl group, and m1 and m2 are each an integer of 1 or 2, such as an integer of 1 can

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] [165] [166]

[167] [168] [169] [170]

[171] [172] [173] [174]

[175] [176] [177] [178]

[179] [180] [181] [182]

[183] [184] [185] [186]

[187] [188] [189] [190]

[191] [192] [193] [194]

[195] [196] [197] [198]

[199] [200] [201] [202]

[203] [204] [205] [206]

[207] [208] [209] [210]

[211] [212] [213] [214]

[215] [216] [217] [218]

[219] [220] [221] [222]

[223] [224] [225] [226]

[227] [228] [229] [230]

[231] [232] [233] [234]

[235] [236] [237]

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 ¹ 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 ³ 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 or a substituted or unsubstituted C2 to C30 heterocyclic group,

m3 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 ² 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 ⁴ to 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 A cyclic C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,

m4, m6, and m8 are each independently an integer of 1 to 4;

m5 and m7 are each independently an integer of 1 or 2;

At least one of R ³ to R ⁸ is a group represented by the following formula (a),

[Formula a]

In the above formula (a),

L ³ to L ⁵ are each independently a single bond or a substituted or unsubstituted C6 to C30 arylene group;

Ar ⁴ and Ar ⁵ 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.

In Formula 2, when m3 is 2 or more, each R ³ may be the same as or different from each other.

In Group II, when m4 is 2 or more, each R ⁴ may be identical to or different from each other.

In Group II, when m5 is 2 or more, each R ⁵ may be identical to or different from each other.

In Group II, when m6 is 2 or more, each R ⁶ may be identical to or different from each other.

In Group II, when m7 is 2 or more, each R ⁷ may be identical to or different from each other.

In Group II, when m8 is 2 or more, each R ⁸ may be identical to or different from each other.

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 ¹ , X ² , m3 to m8, and R ³ to R ⁸ 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-IB to Formula 2-IXB, and Formula 2-IIC to Formula 2-IVC 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]

[Formula 2-IB] [Formula 2-IIB]

[Formula 2-ⅢB] [Formula 2-IVB]

[Formula 2-ⅤB] [Formula 2-VIB]

[Formula 2-VIIB] [Formula 2-VIIIB]

[Formula 2-ⅨB] [Formula 2-IIC]

[Formula 2-IIIC] [Formula 2-IVC]

In Formula 2-IA to Formula 2-IXA, Formula 2-IB to Formula 2-IXB, and Formula 2-IIC to Formula 2-IVC,

X ¹ , X ² , L ³ to L ⁵ , m3 to m8, Ar ⁴ and Ar ⁵ are as described above;

R ³ to R ⁸ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group, or a substituted or unsubstituted C6 to C30 aryl group;

m3', m4', m6' and m8' are each independently an integer from 1 to 3,

m5' is 1.

When m3' is 2 or more, each R ³ may be the same as or different from each other.

When m4' is 2 or more, each R ⁴ may be the same as or different from each other.

When m6' is 2 or more, each R ⁶ may be the same as or different from each other.

When m8' is 2 or more, each R ⁸ may be identical to or different from each other.

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

For example, X ¹ in Formula 2-IVB may be NR ^b .

For example, X ¹ in Formula 2-VIIIB may be O or S, and X ² 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 ³ to L ⁵ are each independently a single bond or a substituted or unsubstituted phenylene group;

Ar ⁴ and Ar ⁵ are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, or a substituted or unsubstituted naphthyl group,

X ¹ is NR ^b , O or S;

X ² 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 ³ , R ⁵ , R ⁶ , R ⁷ , and R ⁸ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group or a substituted or unsubstituted C6 to C30 aryl group,

m3 is an integer from 1 to 4;

m5 and m7 are each independently an integer of 1 or 2;

m6' and m8' are each independently one of integers from 1 to 3.

For example, L ⁴ and L ⁵ may each independently be a single bond, a substituted or unsubstituted phenylene group, or a substituted or unsubstituted biphenylene group.

For example, Ar ⁴ and Ar ⁵ 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]

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

[2-5] [2-6] [2-7]

[2-8] [2-9]

[2-10] [2-11] [2-12]

[2-13] [2-14] [2-15]

[2-16] [2-17]

[2-18] [2-19] [2-20]

[2-21] [2-22]

[2-23] [2-24] [2-25] [2-26]

[2-27] [2-28] [2-29] [2-30]

[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 ⁶ MX ³

In Formula Z, M is a metal, L ⁶ and X ³ 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 a combination thereof, and L ⁶ and X ³ may be, for example, bi It may be a dentate ligand.

Examples of the ligand represented by L ⁶ and X ³ 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, a substituted or unsubstituted C1 to C30 cycloalkyl group, 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 An 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 a substituted or unsubstituted It is a triarylsilyl group having a C6 to C30 aryl group.

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

[Formula I]

In Formula I,

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 1-1 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,

n1 and n2 are independently any one of integers from 0 to 3, n1 + n2 is any one of integers from 1 to 3,

[Formula Ⅰ-1]

In Formula 1-1,

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 ;

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, for example, by Chemical Formula II below.

[Formula II]

In Formula II,

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, metal, metal oxide, and/or 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 1

[Scheme 1]

Step 1: Synthesis of Intermediate A-1

In a round bottom flask, 60.0 g (248.48 mmol) of 1-bromo-5-chloronaphthalene, 42.7 g (248.44 mmol) of 1-naphthaleneboronic acid, 12.17 g (14.91 mmol) of Pd(dppf)Cl ₂ , 85.84 g (621.09 g) of K ₂ CO ₃ mmol), dissolved in 600 mL of THF and 300 mL of distilled water, and heated to reflux under a nitrogen atmosphere. After 12 hours, the reaction solution was cooled, the water layer was removed, and the organic layer was dried under reduced pressure. After washing the obtained solid with water and methanol, the solid was recrystallized with 200 mL of Toluene to obtain 55.0 g (Yield: 77%) of Intermediate A-1.

Step 2: Synthesis of Intermediate A

Intermediate A-1 55.0 g (190.46 mmol), Bis (pinacolato) diboron 48.37 g (190.46 mmol), Pd ₂ (dba) ₃ 10.46 g (11.43 mmol), P (Cy) ₃ 12.82 g (45.71 mmol), and KOAc After dissolving 56.08 g (571.39 mmol) in 600 ml of Xylene, the mixture was stirred under reflux for 12 hours. After the reaction was completed, the reaction solvent was removed with a rotary evaporator, extracted with methylene chloride, and the organic layer was columned with Hexane: EA = 4: 1 (v/v) to obtain 55.0 g (Yield: 76%) of Intermediate A.

LC/MS calculated for: C26H25BO2 Exact Mass 380.29 found for 381.14 [M+H]

Step 3: Synthesis of Compound 1

In a round bottom flask, 13.92 g (30.74 mmol) of intermediate A, 10.0 g (27.95 mmol) of 2-chloro-4-(1-dibenzofuranyl)-6-phenyl-1,3,5-triazine (Int-1), Pd( After putting 0.97 g (0.84 mmol) of PPh ₃ ) ₄ and 7.73 g (55.90 mmol) of K ₂ CO ₃ and dissolving them in 150 mL of THF and 70 mL of distilled water, the mixture was heated to reflux under a nitrogen atmosphere. After 12 hours, the reaction solution was cooled, the water layer was removed, and the organic layer was dried under reduced pressure. After washing the obtained solid with water and methanol, the solid was recrystallized twice with 200 mL of Toluene to obtain 12.0 g (Yield: 81%) of Compound 1.

LC/MS calculated for: C41H25N3O Exact Mass 575.67 found for 576.32 [M+H]

Synthesis of intermediates B to E

Synthesis Example 2: Synthesis of Intermediate B

61.0 g of Intermediate B (Yield: 80%) was obtained by synthesizing in the same manner as in Steps 1 and 2 of Synthesis Example 1, except that the same equivalent amount of phenylboronic acid was used instead of 1-naphthaleneboronic acid in Step 1 of Synthesis Example 1. .

LC/MS calculated for: C22H23BO2 Exact Mass 330.23 found for 330.85 [M+H]

Synthesis Example 3: Synthesis of Intermediate C

Intermediate C was synthesized in the same manner as in Steps 1 and 2 of Synthesis Example 1, except that the same equivalent of dibenzo[b,d]furan-1-ylboronic acid was used instead of 1-naphthaleneboronic acid in Step 1 of Synthesis Example 1. 55.0 g (Yield: 78%) was obtained.

LC/MS calculated for: C28H25BO3 Exact Mass 420.32 found for 420.65 [M+H]

Synthesis Example 4: Synthesis of Intermediate D

Intermediate D 52.0 g (Yield: 74 %) was obtained.

LC/MS calculated for: C30H27BO2 Exact Mass 430.35 found for 431.11 [M+H]

Synthesis Example 5: Synthesis of Intermediate E

[Scheme 2]

Step 1: Synthesis of Intermediate E-1

After dissolving 50.0 g (174.84 mmol) of 1,8-dibromonaphthalene and 15.66 g (174.84 mmol) of Copper(I) cyanide in 1000 ml of DMF, the mixture was heated under reflux at 150°C for 12 hours under a nitrogen atmosphere. After the reaction was completed, the reaction solvent was removed with a rotary evaporator, extracted with methylene chloride, and the organic layer was columned with Hexane : EA = 4 : 1 (v/v) to obtain 30.0 g (Yield: 74%) of Intermediate E-1.

Step 2: Synthesis of Intermediate E-2

In a round bottom flask, 30.0 g (129.27 mmol) of intermediate E-1, 32.38 g (129.27 mmol) of Bis(pinacolato) diboron, _7.10 g (7.76 mmol) of Pd ₂ (dba) ₃ , 8.70 g (31.08 mmol) of P(Cy) 3 ), and 38.06 g (387.80 mmol) of KOAc were dissolved in 350 ml of Xylene, followed by reflux stirring for 12 hours. After the reaction was completed, the reaction solvent was removed with a rotary evaporator, extracted with methylene chloride, and the organic layer was columned with Hexane : EA = 4 : 1 (v/v) to obtain 45.0 g (Yield: 77%) of Intermediate E-2.

Step 3: Synthesis of Intermediate E-3

In a round bottom flask, 32.0 g (132.50 mmol) of 1-bromo-5-chloronaphthalene, 44 g (132.50 mmol) of intermediate E-2, 4.59 g (3.97 mmol) of Pd(PPh ₃ ) ₄ , and 36.63 g of K ₂ CO ₃ ( 265.0 mmol), dissolved in 600 mL of THF, and 300 mL of distilled water, and heated to reflux under a nitrogen atmosphere. After 12 hours, the reaction solution was cooled, the water layer was removed, and the organic layer was dried under reduced pressure. After washing the obtained solid with water and methanol, the solid was recrystallized with 200 mL of toluene to obtain 38.0 g of intermediate E-3 (Yield: 76%).

Step 4: Synthesis of Intermediate E

Intermediate E-3 38.0 g (121.10 mmol), Bis(pinacolato)diboron 30.75 g (121.10 mmol), Pd ₂ (dba) ₃ 6.65 g (7.27 mmol), P(Cy) ₃ 8.15 g (29.06 mmol), and KOAc After dissolving 35.66 g (363.31 mmol) in 350 ml of Xylene, the mixture was stirred under reflux for 12 hours. After the reaction was completed, the reaction solvent was removed with a rotary evaporator, extracted with methylene chloride, and the organic layer was columned with Hexane : EA = 4 : 1 (v/v) to obtain 35.0 g of Intermediate E (Yield: 71%).

LC/MS calculated for: C27H24BNO2 Exact Mass 405.30 found for 405.77 [M+H]

Synthesis Examples 6 to 9

In step 3 of Synthesis Example 1, Intermediates B to E were used instead of Intermediate A, and Int-1 or Int-2 was reacted in the same manner as in Synthesis Example 1 to synthesize compounds according to Table 1 below.

Comparative Synthesis Example 1: Synthesis of Intermediate F

[Scheme 3]

Step 1: Synthesis of Intermediate F-1

(3-mercaptonaphthalen-2-yl)boronic acid (6.88g, 28.32 mmol), Pd(PPh ₃ ) ₄ (1.4 g, 1.21 mmol) in 1,5-dibromo-2,4-difluorobenzene (10.0 g, 36.78 mmol) ), K ₂ CO ₃ (11.18 g, 80.92 mmol), THF (200 ml), and H ₂ O (100 ml) were added and synthesized in the same manner as in Step 1 of Synthesis Example 1 to obtain 9.0 g of Intermediate F-1 ( Yield: 63%).

Step 2: Synthesis of Intermediate F-2

3-nitropyridine (0.30 g, 2.05 mmol), Pd(OAc) ₂ (0.46 g, 2.05 mmol), tert-butyl peroxybenzoate (18.66 g, 46.13 mmol), C ₆ in intermediate F-1 (9.00 g, 25.63 mmol) F ₆ (100 ml) and 1,3-dimethyl-2-imidazolidinone (100 ml) were added and heated under reflux at 90°C for 12 hours. After the reaction was completed, the reaction solvent was removed by a rotary evaporator, extracted with Methylene Chloride, and the organic layer was dried with MgSO ₄ and concentrated. got

Step 3: Synthesis of Intermediate F-3

Intermediate F-2 7.0 g (21.14 mmol), Bis(pinacolato)diboron 5.37 g (21.14 mmol), Pd ₂ (dba) ₃ 1.16 g (1.27 mmol), P(Cy) ₃ 1.42 g (5.07 mmol), and KOAc After dissolving 6.22 g (63.41 mmol) in 100 ml of Xylene, the mixture was stirred under reflux for 12 hours. After the reaction was completed, the reaction solvent was removed with a rotary evaporator, extracted with methylene chloride, and the organic layer was columned with Hexane : EA = 4 : 1 (v/v) to obtain 7.0 g (Yield: 88%) of intermediate F-3.

Step 4: Synthesis of Intermediate F-4

2-bromo-3-chlorophenol (3.2 g, 15.43 mmol), intermediate F-3 (7.0 g, 15.43 mmol), Pd(PPh ₃ ) ₄ (0.53 g, 0.46 mmol), K ₂ CO ₃ (4.26 g, 30.85 mmol), THF (80 ml), and H ₂ O (40 ml) were added thereto and synthesized in the same manner as in Synthesis Example 1, step 1, to obtain 5.3 g of intermediate F-4 (Yield: 90%).

Step 5: Synthesis of Intermediate F-5

3-nitropyridine (0.17 g, 1.12 mmol), Pd(OAc) ₂ (0.25 g, 1.12 mmol), tert-butyl peroxybenzoate (10.19 g, 25.18 mmol), C ₆ in intermediate F-4 (5.30 g, 13.99 mmol) F ₆ (50 ml) and 1,3-dimethyl-2-imidazolidinone (50 ml) were added and synthesized in the same manner as in Step 2 of Comparative Synthesis Example 1, and 4.0 g of intermediate F-5 (Yield: 80%) was obtained.

Step 6: Synthesis of Intermediate F-6

Intermediate F-5 4.0 g (11.15 mmol), Bis(pinacolato)diboron 2.83 g (11.15 mmol), Pd ₂ (dba) ₃ 0.61 g (0.67 mmol), P(Cy) ₃ 0.75 g (2.68 mmol), and KOAc After dissolving 3.28 g (33.44 mmol) in 40 ml of Xylene, it was synthesized in the same manner as in Step 3 of Comparative Synthesis Example 1 to obtain 4.2 g (Yield: 84%) of Intermediate F-6.

LC/MS calculated for: C28H23BO3S Exact Mass 450.36 found for 450.81 [M+H]

Step 7: Synthesis of Intermediate F-7

In a round bottom flask, intermediate F-6 (4.2 g, 17.39 mmol) 1-bromo-5-chloronaphthalene 7.83 g (17.39 mmol), Pd(PPh ₃ ) ₄ (0.6 g, 0.52 mmol), and K ₂ CO ₃ (4.81 g, 34.78 mmol) was dissolved in 90 ml of THF and 45 ml of H ₂ O, and heated to reflux under a nitrogen atmosphere. After 12 hours, the reaction solution was cooled, the water layer was removed, and the organic layer was dried under reduced pressure. After washing the obtained solid with MeOH, the solid was recrystallized from toluene to obtain 7.5 g of intermediate F-7 (Yield: 89%).

Step 8: Synthesis of Intermediate F

Intermediate F-7 7.5 g (15.46 mmol), Bis(pinacolato)diboron 4.12 g (16.24 mmol), Pd ₂ (dba) ₃ 0.85 g (0.06 mmol), P(Cy) ₃ 4.55 g (46.39 mmol), and KOAc After dissolving 4.55 g (46.39 mmol) in 50 ml of Xylene, the mixture was stirred under reflux for 12 hours. After the reaction was completed, the reaction solvent was removed with a rotary evaporator, extracted with methylene chloride, and the organic layer was columned with Hexane : EA = 4 : 1 (v/v) to obtain 7.7 g (89% Yield) of Intermediate F.

LC/MS calculated for: C38H29BO3S Exact Mass 576.19 found for 576.54 [M+H]

Synthesis of intermediates G to J

Comparative Synthesis Example 2: Synthesis of Intermediate G

55.0 g of Intermediate G synthesized in the same manner as in Steps 1 and 2 of Synthesis Example 1, except that the same amount of 1-bromo-4-chloronaphthalene was used instead of 1-bromo-5-chloronaphthalene in Step 1 of Synthesis Example 1. (Yield: 84%) was obtained.

LC/MS calculated for: C26H25BO2 Exact Mass 380.29 found for 381.11 [M+H]

Comparative Synthesis Example 3: Synthesis of Intermediate H

Intermediate H 58.0 g was synthesized in the same manner as in Steps 1 and 2 of Synthesis Example 1, except that the same amount of 2-bromo-1-chloronaphthalene was used instead of 1-bromo-5-chloronaphthalene in Step 1 of Synthesis Example 1. (Yield: 88%) was obtained.

LC/MS calculated for: C26H25BO2 Exact Mass 380.29 found for 380.87 [M+H]

Comparative Synthesis Example 4: Synthesis of Intermediate I

Intermediate I 57.0 g was synthesized in the same manner as in Steps 1 and 2 of Synthesis Example 1, except that the same amount of 1-bromo-6-chloronaphthalene was used instead of 1-bromo-5-chloronaphthalene in Step 1 of Synthesis Example 1. (Yield: 87%) was obtained.

LC/MS calculated for: C26H25BO2 Exact Mass 380.29 found for 380.58 [M+H]

Comparative Synthesis Example 5: Synthesis of Intermediate J

55.0 g of Intermediate J was synthesized in the same manner as in Steps 1 and 2 of Synthesis Example 1, except that the same amount of 2-bromo-6-chloronaphthalene was used instead of 1-bromo-5-chloronaphthalene in Step 1 of Synthesis Example 1. (Yield: 84%) was obtained.

LC/MS calculated for: C26H25BO2 Exact Mass 380.29 found for 380.84 [M+H]

Comparative Synthesis Examples 6 to 10

C-1 C-2 C-3

C-4 C-5

In step 3 of Synthesis Example 1, Intermediate G to Intermediate J were used instead of Intermediate A, and Int-1 or Int-2 was reacted in the same manner as in Synthesis Example 1 to synthesize compounds according to Table 1 below.

synthesis example Int A Int-1 final
product yield
(transference number) of the final product
property data Synthesis Example 6 Intermediate B Int-1 compound 3 12.0g, (81%) LC/MS calculated for: C37H25N3O Exact Mass: 527.63 found for 528.15 [M+H] Synthesis Example 7 Intermediate C Int-1 compound 5 14.0g, (81%) LC/MS calculated for: C43H25N3O2 Exact Mass: 615.69 found for 616.21 [M+H] Synthesis Example 8 Intermediate D Int-1 compound 6 13.0g, (74%) LC/MS calculated for: C45H27N3O Exact Mass: 625.73 found for 626.22 [M+H] Synthesis Example 9 Intermediate E Int-1 compound 9 12.8g, (76%) LC/MS calculated for: C42H24N4O Exact Mass: 600.68 found for 600.83 [M+H] Comparative Synthesis Example 6 Intermediate F Int-2 compound C-1 6.0 g (86%) LC/MS calculated for: C47H27N3OS Exact Mass: 681.19 found for 681.42 [M+H] Comparative Synthesis Example 7 Intermediate G Int-1 compound C-2 12.8g, (80%) LC/MS calculated for: C41H25N3O Exact Mass: 575.67 found for 576.33 [M+H] Comparative Synthesis Example 8 Intermediate H Int-1 compound C-3 11.5g, (71%) LC/MS calculated for: C41H25N3O Exact Mass: 575.67 found for 576.28 [M+H] Comparative Synthesis Example 9 Intermediate I Int-1 compound C-4 12.5g, (78%) LC/MS calculated for: C41H25N3O Exact Mass: 575.67 found for 576.12[M+H] Comparative Synthesis Example 10 Intermediate J Int-1 compound C-5 13.2g, (82%) LC/MS calculated for: C41H25N3O Exact Mass: 575.67 found for 576.94 [M+H]

Synthesis Example 10: Synthesis of Compound A-84

[Scheme 4]

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. After the reaction is completed, 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 11: Synthesis of Compound 2-92

[Scheme 5]

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 100 ml of toluene, and 0.47 g (0.51 mmol) of Pd (dba) ₂ 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 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) was washed with ultrasonic waves in 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 having a thickness of 100 Å, and the hole injection layer A hole transport layer was formed by depositing compound A on top to a thickness of 1300 Å. 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 1 obtained in Synthesis Example 1 was used as a host on the hole transport auxiliary layer and doped with 2 wt% of [Ir(piq)2acac] as a dopant to form a light emitting layer having a thickness of 400 Å by vacuum deposition. In the case of the following Examples and Comparative Examples, the ratio was separately described. 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 diode was fabricated by forming a cathode by sequentially vacuum depositing 15 Å of LiQ and 1200 Å of Al on the electron transport layer.

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

ITO / Compound A (3% NDP-9 doping, 100Å) / Compound A (1300Å) / Compound B (350Å) / EML [Compound 1: [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 5

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

Examples 6 to 15 and Comparative Examples 6 to 11

As shown in Table 3 below, the host was changed, but the first host and the second host were mixed at a weight ratio of 5:5, and Examples 6 to 15 and Comparative Examples 6 to 11 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 11 were evaluated. The specific measurement method is as follows, and the results are shown in Tables 2 and 3.

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

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

(3) Measurement of luminous efficiency

Luminous 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 2 and Comparative Example 7 were calculated and shown in Tables 2 and 3 below.

(4) 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 voltage of Comparative Example 7 were calculated and shown in Table 3 below.

division sole host Luminous efficiency (%) Example 1 compound 1 192 Example 2 compound 3 154 Example 3 compound 5 185 Example 4 compound 6 138 Example 5 compound 9 192 Comparative Example 1 compound C-1 77 Comparative Example 2 compound C-2 100 Comparative Example 3 compound C-3 77 Comparative Example 4 compound C-4 62 Comparative Example 5 compound C-5 46

division host Driving voltage (%) Luminous efficiency (%) first host 2nd host Example 6 One A-84 79 179 Example 7 3 A-84 75 143 Example 8 5 A-84 67 171 Example 9 6 A-84 75 129 Example 10 9 A-84 58 179 Example 11 One 2-92 71 171 Example 12 3 2-92 67 132 Example 13 5 2-92 58 164 Example 14 6 2-92 67 121 Example 15 9 2-92 50 168 Comparative Example 6 C-1 A-84 83 71 Comparative Example 7 C-3 A-84 100 100 Comparative Example 8 C-5 A-84 75 50 Comparative Example 9 C-1 2-92 75 68 Comparative Example 10 C-3 2-92 92 93 Comparative Example 11 C-5 2-92 63 54

Referring to Tables 2 and 3, when the compound according to the present invention is used as a single host and a mixed host in combination with a second host, it can be seen that the luminous efficiency and / or driving voltage 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 (14)

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

In Formula 1,
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 and L ² are each independently a single bond, a substituted or unsubstituted C6 to C30 arylene group or a substituted or unsubstituted C2 to C30 heterocyclic 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,
Ar ³ is a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted pyrimidinyl group, a substituted or unsubstituted triazinyl group, a substituted or unsubstituted dibenzofuranyl group, A substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted benzonaphthofuranyl group, or a substituted or unsubstituted benzonaphthothiophenyl group,
R ^a , R ¹ and R ² are each independently hydrogen, deuterium, 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 one of integers from 1 to 3,
When m2 is 2 or more, each R ² is independently present or adjacent R ² are fused to form a ring. According to claim 1,
Formula 1 is a compound for an organic optoelectronic device represented by Formula 1-1 or Formula 1-2:
[Formula 1-1] [Formula 1-2]

In Formula 1-1 and Formula 1-2,
Z ¹ to Z ³ , L ¹ , L ² , Ar ¹ to Ar ³ , R ¹ and m1 are as defined in claim 1,
R ^2a , R ^2b , R ^2c , R ^2d , R ^2e , R ^2f and R ^2g are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, or a substituted or unsubstituted C6 to C20 aryl group. . 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 terphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, A substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted benzophenanthrenyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted group substituted dibenzosilolyl group, substituted or unsubstituted dibenzofuranyl group, substituted or unsubstituted dibenzothiophenyl group, substituted or unsubstituted carbazolyl group, substituted or unsubstituted benzonaphthofuranyl group, substituted or unsubstituted Cyclized benzonaphthothiophenyl group, substituted or unsubstituted dinaphthofuranyl group, substituted or unsubstituted dinaphthothiophenyl group, substituted or unsubstituted fused dibenzofuranyl group, substituted or unsubstituted fused dibenzothiophene Dial, substituted or unsubstituted benzocarbazinyl group, substituted or unsubstituted phenoxazinyl group, substituted or unsubstituted thiophenoxazinyl group, substituted or unsubstituted benzophenoxazinyl group, substituted or unsubstituted benzothiophene Noxazinyl group, substituted or unsubstituted 10-phenyl-10H-spiro[acridine-9,9'-fluorenyl group], substituted or unsubstituted 10H -spiro[acridine-9,9 '-fluorenyl group], or a substituted or unsubstituted spiro[fluorene-9,9'-xanthenyl group], a compound for an organic optoelectronic device. According to claim 1,
Ar ³ is a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, or a substituted or unsubstituted phenan A trenyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted benzonaphthofuranyl group, a substituted or unsubstituted benzo A naphthothiophenyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted pyrimidinyl group, or a substituted or unsubstituted triazinyl group, a compound for an organic optoelectronic device. According to claim 1,
Wherein L ¹ and L ² are each independently a single bond, a substituted or unsubstituted phenylene group, a substituted or unsubstituted biphenylene group, a substituted or unsubstituted naphthylene group, a substituted or unsubstituted phenanthrenylene group, or a substituted Or an unsubstituted dibenzofuranylene group or a substituted or unsubstituted dibenzothiophenylene group, a compound for an organic optoelectronic device. According to claim 1,
Wherein *-L ¹ -Ar ¹ and *-L ² -Ar ² are each independently one selected from substituents listed in Group I, Compound for Organic Optoelectronic Device:
[Group I]

In Group I above, * is a connection point. According to claim 1
A compound for an organic optoelectronic device selected from among the compounds listed in Group 1 below:
[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] [165] [166]

[167] [168] [169] [170]

[171] [172] [173] [174]

[175] [176] [177] [178]

[179] [180] [181] [182]

[183] [184] [185] [186]

[187] [188] [189] [190]

[191] [192] [193] [194]

[195] [196] [197] [198]

[199] [200] [201] [202]

[203] [204] [205] [206]

[207] [208] [209] [210]

[211] [212] [213] [214]

[215] [216] [217] [218]

[219] [220] [221] [222]

[223] [224] [225] [226]

[227] [228] [229] [230]

[231] [232] [233] [234]

[235] [236] [237]

. 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 ¹ 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 ³ 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 or a substituted or unsubstituted C2 to C30 heterocyclic group,
m3 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 ² 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 ⁴ to R ⁸ are each independently hydrogen, deuterium, a substituted or unsubstituted amine group, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted A cyclic C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,
m4, m6, and m8 are each independently an integer of 1 to 4;
m5 and m7 are each independently an integer of 1 or 2;
At least one of R ³ to R ⁸ is a group represented by the following formula (a),
[Formula a]

In the above formula (a),
L ³ to L ⁵ are each independently a single bond or a substituted or unsubstituted C6 to C30 arylene group;
Ar ⁴ and Ar ⁵ 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 ¹ , X ² , R ³ to R ¹² are as defined in claim 7. According to claim 9,
The second compound is an organic optoelectronic device composition represented by any one of the following Formulas 2-IA to 2-IXA, Formula 2-IB to Formula 2-IXB, and Formula 2-IIC to Formula 2-IVC:
[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]

[Formula 2-IB] [Formula 2-IIB]

[Formula 2-ⅢB] [Formula 2-IVB]

[Formula 2-ⅤB] [Formula 2-VIB]

[Formula 2-VIIB] [Formula 2-VIIIB]

[Formula 2-ⅨB] [Formula 2-IIC]

[Formula 2-IIIC] [Formula 2-IVC]

In Formula 2-IA to Formula 2-IXA, Formula 2-IB to Formula 2-IXB, and Formula 2-IIC to Formula 2-IVC,
X ¹ , X ² , L ³ to L ⁵ , m3 to m8, Ar ⁴ and Ar ⁵ are as defined in claim 8,
R ³ to R ⁸ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group, or a substituted or unsubstituted C6 to C30 aryl group;
m3', m4', m6' and m8' are each independently an integer from 1 to 3,
m5' is 1. 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 ³ to L ⁵ are each independently a single bond or a substituted or unsubstituted phenylene group;
Ar ⁴ and Ar ⁵ are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, or a substituted or unsubstituted naphthyl group,
X ¹ is NR ^b , O or S;
X ² 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 ³ , R ⁵ , R ⁶ , R ⁷ , and R ⁸ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group or a substituted or unsubstituted C6 to C30 aryl group,
m3 is an integer from 1 to 4;
m5 and m7 are each independently an integer of 1 or 2;
m6' and m8' 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 11. According to claim 12,
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 12 .

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