KR102235262B1 - Organic compound and composition and organic optoelectronic device and display device - Google Patents

Abstract

상기 화학식 1에서, X¹, X², Ar¹, Ar², L¹ 및 R¹ 내지 R⁶은 명세서에 기재한 바와 같다.It relates to an organic compound represented by the following Formula 1, a composition including the same, an organic optoelectronic device, and a display device.
[Formula 1]

In Formula 1, X ¹ , X ² , Ar ¹ , Ar ² , L ¹ and R ¹ to R ⁶ are as described in the specification.

Description

An organic compound, a composition, an organic optoelectronic device, and a display device TECHNICAL FIELD [ORGANIC COMPOUND AND COMPOSITION AND ORGANIC OPTOELECTRONIC DEVICE AND DISPLAY DEVICE}

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

An organic optoelectronic diode is a device capable of converting electrical energy and optical energy to each other.

Organic optoelectronic devices can be roughly divided into two types according to the principle of operation. One is a photoelectric device that generates electrical energy by separating the excitons formed by light energy into electrons and holes, and the electrons and holes are transferred to different electrodes, and the other is electrical energy by supplying voltage or current to the electrode. 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) are attracting great attention in recent years due to an increase in demand for flat panel display devices. The organic light-emitting device is a device that converts electrical energy into light, and the performance of the organic light-emitting device is greatly influenced by an organic material positioned between electrodes.

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

Another embodiment provides a composition capable of implementing a high efficiency and long life organic optoelectronic device.

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

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

According to one embodiment, an organic compound represented by the following formula (1) is provided.

[Formula 1]

In Formula 1,

X ¹ and X ² are each independently O or S,

Ar ¹ and Ar ² are each independently a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof,

L ¹ is a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C6 to C30 arylene group, or a combination thereof,

R ¹ to R ⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heterocyclic group, a cyano group, or these It is a combination of.

According to another embodiment, a composition comprising the first organic compound and a second organic compound including a carbazole moiety represented by the following Chemical Formula 4 is provided.

[Formula 4]

In Chemical Formula 4,

Y ¹ is a single bond, a substituted or unsubstituted C6 to C30 arylene group or a divalent substituted or unsubstituted C2 to C30 heterocyclic group,

A ¹ is a substituted or unsubstituted C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,

R ⁹ to R ¹⁴ are each Independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heterocyclic group,

R ⁹ and R ¹⁰ are each Exist independently or fuse with each other to form a ring,

R ¹¹ to R ¹⁴ are each They exist independently, or ^{adjacent groups among R 11} to R ¹⁴ are connected to each other to form a ring.

According to another embodiment, an anode and a cathode facing each other, and an organic layer disposed between the anode and the cathode, wherein the organic layer provides an organic optoelectronic device including the organic compound or the composition.

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

High-efficiency, long-life organic optoelectronic devices can be implemented.

1 and 2 are cross-sectional views each illustrating an organic light-emitting device according to an 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 the present specification, unless otherwise defined, "substituted" 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 It means substituted by 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, "substituted" 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, and a C2 to C30 heteroaryl 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 C2 to C30 heteroaryl group. In addition, in a specific example of the present invention, "substitution" means that at least one hydrogen in a substituent or compound is deuterium, a C1 to C5 alkyl group, a C6 to C18 aryl group, a pyridinyl group, a quinolinyl group, an isoquinolinyl group, a di It means substituted with a benzofuranyl group, a dibenzothiophenyl group, or a carbazolyl 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, a dibenzofuranyl group, or a dibenzothiophenyl group. it means. In addition, in a specific example of the present invention, "substitution" means that at least one hydrogen in a substituent or compound is deuterium, methyl group, ethyl group, propanyl group, butyl group, phenyl group, biphenyl group, terphenyl group, naphthyl group, triphenyl group, di It means substituted with a benzofuranyl group or a dibenzothiophenyl group.

In the present specification, "hetero" means that one functional group contains 1 to 3 heteroatoms selected from the group consisting of N, O, S, P, and Si, and the rest is carbon, unless otherwise defined. .

In the present specification, "aryl group" is a concept that encompasses a group having one or more hydrocarbon aromatic moieties, and while all elements of the hydrocarbon aromatic moiety have p-orbitals, these p-orbitals are conjugated. Forms forming, for example, a phenyl group, a naphthyl group, etc., and two or more hydrocarbon aromatic moieties are linked through a sigma bond, including a biphenyl group, a terphenyl group, a quaterphenyl group, etc., and two or more hydrocarbon aromatic moieties They may contain directly or indirectly fused non-aromatic fused rings such as fluorenyl groups and the like. Aryl groups include monocyclic, polycyclic or fused ring polycyclic (ie, rings that share adjacent pairs of carbon atoms) functional groups.

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

For example, "heteroaryl group" means containing at least one hetero atom selected from the group consisting of N, O, S, P, and Si in the aryl group. Two or more heteroaryl groups are directly connected through a sigma bond, or when the heteroaryl group includes two or more rings, 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 heteroatoms.

The heterocyclic group may include, for example, a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, and the like.

More specifically, a substituted or unsubstituted C6 to C30 aryl group and/or a substituted or unsubstituted C2 to C30 heterocyclic group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthra Senyl group, substituted or unsubstituted phenanthrenyl group, substituted or unsubstituted naphthacenyl group, substituted or unsubstituted pyrenyl group, substituted or unsubstituted biphenyl group, substituted or unsubstituted p-terphenyl group, substituted or unsubstituted A substituted m-terphenyl group, a substituted or unsubstituted o-terphenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted perylenyl group, a substituted or unsubstituted flu Orenyl group, substituted or unsubstituted indenyl group, substituted or unsubstituted furanyl group, substituted or unsubstituted thiophenyl group, substituted or unsubstituted pyrrolyl group, substituted or unsubstituted pyrazolyl group, substituted or unsubstituted already Dazolyl group, substituted or unsubstituted triazolyl group, substituted or unsubstituted oxazolyl group, substituted or unsubstituted thiazolyl group, substituted or unsubstituted oxadiazolyl group, 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 unsubstituted benzo Thiophenyl group, substituted or unsubstituted benzimidazolyl group, substituted or unsubstituted indolyl group, substituted or unsubstituted quinolinyl group, substituted or unsubstituted isoquinolinyl group, substituted or unsubstituted quinazolinyl group, substituted Or an unsubstituted quinoxalinyl group, a substituted or unsubstituted naphthyridinyl group, a substituted or unsubstituted benzoxazineyl group, a substituted or unsubstituted benzthiazinyl group, a substituted or unsubstituted acridinyl group, a substituted or unsubstituted Phenazineyl group, substituted or unsubstituted phenothiazinyl group, substituted or unsubstituted phenoxazineyl group, substituted or unsubstituted dibenzofuranyl group, or substituted or unsubstituted dibenzothiophenyl group, or a combination thereof May be, but is not limited thereto.

In the present specification, the hole property refers to a property capable of forming holes by donating electrons when an electric field is applied, and injection of holes formed at the anode into the emission layer with conduction characteristics according to the HOMO level, and the emission layer It means a property that facilitates the movement of the holes formed in the anode to the anode and the movement in the light emitting layer.

In addition, electronic properties refer to the property of receiving electrons when an electric field is applied, and has conduction properties according to the LUMO level, so that electrons formed at the cathode are injected into the emission layer, electrons formed at the emission layer move to the cathode, and in the emission layer. It refers to the property that facilitates the movement of.

Hereinafter, an organic compound according to an embodiment will be described.

An organic compound according to an embodiment is represented by the following formula (1).

[Formula 1]

In Formula 1,

X ¹ and X ² are each independently O or S,

Ar ¹ and Ar ² are each independently a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof,

L ¹ is a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C6 to C30 arylene group, or a combination thereof,

R ¹ to R ⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heterocyclic group, a cyano group, or these It is a combination of.

The organic compound represented by Formula 1 may exhibit rapid electron transport properties by including a substituted pyrimidine ring and a fused ring in which benzofuran or benzothiophene is bonded, and dibenzofuran as a benzofuran or benzothiophene side of the fused ring. By combining a yl group or a dibenzothiophenyl group, a faster electron transport property may be exhibited. Accordingly, when the organic compound is applied to a device, a device having a low driving voltage and high efficiency can be implemented.

In addition, since the organic compound represented by Formula 1 has a relatively high glass transition temperature, when the organic compound is applied to a device, it is possible to improve thermal stability and improve the life of the device by reducing or preventing deterioration of the organic compound during processing or driving. have. For example, the organic compound may have a glass transition temperature of about 50 to 300°C.

For example, X ¹ and X ² in Formula 1 may be the same or different. For example, X ¹ and X ² may be the same, X ¹ and X ² may be O, and X ¹ and X ² may be S, respectively. For example, X ¹ and X ² may be different and X ¹ may be S and X ² may be O or X ¹ may be O and X ² may be S.

For example, Ar ¹ and Ar ² in Formula 1 may each independently be a substituted or unsubstituted C6 to C30 aryl group, such as a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted group It may be a phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, or a substituted or unsubstituted triphenylene group. Here, the substitution may be one in which at least one hydrogen is substituted with deuterium, a C1 to C20 alkyl group, a C6 to C12 aryl group, or a cyano group.

For example, L ¹ may be a single bond or a substituted or unsubstituted C6 to C30 arylene group. For example, L ¹ is a single bond, a substituted or unsubstituted phenylene group, a substituted or unsubstituted biphenylene group, a substituted or unsubstituted terphenylene group, a substituted or unsubstituted naphthylene group, or a substituted or unsubstituted anthracenylene It can be a flag. For example, L ¹ may be a single bond or a substituted or unsubstituted phenylene group. Here, the substitution may be one in which at least one hydrogen is substituted with deuterium, a C1 to C20 alkyl group, a C6 to C12 aryl group, or a cyano group.

For example, R ¹ to R ⁶ may each independently be hydrogen, a cyano group, a C1 to C20 alkyl group, a C6 to C30 aryl group, and a C6 to C30 aryl group substituted with a cyano group.

For example, R ¹ to R ⁶ may each independently be hydrogen, a cyano group, a C1 to C4 alkyl group, a C6 to C12 aryl group, or a C6 to C12 aryl group substituted with a cyano group.

The organic compound may be, for example, represented by any one of Formulas 2 to 5, but is not limited thereto.

[Formula 2] [Formula 3]

[Formula 4] [Formula 5]

In Formulas 2 to 5, X ¹ , X ² , Ar ¹ , Ar ² and R ¹ to R ⁶ are as described above.

The organic compound may be, for example, represented by any one of Formulas 2a to 2d, 3a to 3d, 4a to 4d, and 5a to 5d, but is not limited thereto.

[Formula 2a] [Formula 2b]

[Formula 2c] [Formula 2d]

[Formula 3a] [Formula 3b]

[Formula 3c] [Formula 3d]

[Formula 4a] [Formula 4b]

[Formula 4c] [Formula 4d]

[Formula 5a] [Formula 5b]

[Formula 5c] [Formula 5d]

In Formulas 2a to 2d, 3a to 3d, 4a to 4d and 5a to 5d, X ¹ , X ² , Ar ¹ , Ar ² and R ¹ to R ⁶ are as described above.

For example, in Formulas 2a to 2d, 3a to 3d, 4a to 4d, and 5a to 5d, L ¹ may be a single bond or a substituted or unsubstituted phenylene group.

For example, in Formulas 2a to 2d, 3a to 3d, 4a to 4d, and 5a to 5d, L ¹ may be a single bond.

The organic compound may be, for example, one selected from compounds listed in Group 1, but is not limited thereto.

[Group 1]

The above-described organic compound may be applied alone or in combination with other organic compounds to an organic optoelectronic device. When the above-described organic compound is used together with other organic compounds, it may be applied in the form of a composition.

Hereinafter, a composition according to an embodiment will be described.

The composition according to an embodiment may include the aforementioned organic compound (hereinafter referred to as “first organic compound”) and an organic compound having hole characteristics (hereinafter referred to as “second organic compound”).

The second organic compound may include, for example, a carbazole moiety, and may be a substituted or unsubstituted carbazole compound, a substituted or unsubstituted biscarbazole compound, or a substituted or unsubstituted indolocarbazole compound. It is not limited.

For example, the second organic compound may include a carbazole moiety represented by Formula 4 below.

[Formula 4]

In Chemical Formula 4,

Y ¹ is a single bond, a substituted or unsubstituted C6 to C30 arylene group or a divalent substituted or unsubstituted C2 to C30 heterocyclic group,

A ¹ is a substituted or unsubstituted C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,

R ⁹ to R ¹⁴ are each Independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heterocyclic group,

R ⁹ and R ¹⁰ are each Exist independently or fuse with each other to form a ring,

R ¹¹ to R ¹⁴ are each They exist independently, or ^{adjacent groups among R 11} to R ¹⁴ are connected to each other to form a ring.

For example, in the definition of Formula 4, the substitution may be one in which at least one hydrogen is substituted with a deuterium, a C1 to C10 alkyl group, a C6 to C12 aryl group, or a C2 to C10 heteroaryl group, for example, at least one hydrogen is deuterium, a phenyl group, It may be substituted with ortho-biphenyl group, meta-biphenyl group, para-biphenyl group, terphenyl group, naphthyl group, dibenzofuranyl group or dibenzothiophenyl group.

For example, the second organic compound may be a compound represented by Formula 4A below.

[Formula 4A]

In Formula 4A,

Y ¹ and Y ² may each independently be a single bond, a substituted or unsubstituted C6 to C30 arylene group, a divalent substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,

A ¹ and A ² may each independently be a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,

R ⁹ to R ¹¹ and R ¹⁵ to R ¹⁷ are each Independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,

m may be an integer of 0 to 2.

For example, Y ¹ and Y ² of Formula 4A may each independently be a single bond, a substituted or unsubstituted phenylene group, or a substituted or unsubstituted biphenylene group, such as a single bond, meta-phenylene group, para-phenyl It may be a ene group, a meta-biphenylene group, or a para-biphenylene group.

For example, A ¹ and A ² in Formula 4A may be a substituted or unsubstituted C6 to C30 aryl group. For example, the aryl group may be selected from a phenyl group, a biphenyl group, a terphenyl group, or a naphthyl group. In addition, A ¹ and A ² of Formula 4A 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, or substituted or unsubstituted triphenylene group, substituted or unsubstituted pyridinyl group, substituted or unsubstituted dibenzothiophenyl group, substituted or unsubstituted dibenzofuranyl group, substituted or unsubstituted carba It may be a zolyl group, a substituted or unsubstituted fluorenyl group, or a combination thereof. For example, A ¹ and A ² in Formula 4A are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted dibenzofuranyl group or a substituted Or it may be an unsubstituted carbazolyl group.

For example, R ⁹ to R ¹¹ and R ¹⁵ to R ¹⁷ of Formula 4A may be hydrogen, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heterocyclic group, for example, all may be hydrogen. have.

For example, m in Formula 4A may be 0 or 1, and for example, m may be 0.

For example, in Formula 4A, the bonding position of the two carbazole groups may be a 2,3-bond, a 3,3-bond, or a 2,2-bond, such as a 3,3-bond.

For example, the compound represented by Formula 4A may be represented by Formula 4A-1 below.

[Formula 4A-1]

In Formula 4A-1, Y ¹ , Y ² , A ¹ , A ² , R ⁹ to R ¹¹ and R ¹⁵ to R ¹⁷ are as described above.

As an example, the compound represented by Formula 4A may be a compound in which one of the carbazole cores listed in Group 2 below and a substituent listed in Group 3 (*-Y ¹ -A ¹ and *-Y ² -A ² ) are combined. However, it is not limited thereto.

[Group 2]

[Group 3]

In groups 2 and 3, * is a connection point.

For example, the compound represented by Formula 4A may be, for example, one of the compounds listed in Group 4, but is not limited thereto.

[Group 4]

[E-1] [E-2] [E-3] [E-4] [E-5]

[E-6] [E-7] [E-8] [E-9] [E-10]

[E-6] [E-7] [E-8] [E-9] [E-10]

[E-11] [E-12] [E-13] [E-14] [E-15]

[E-11] [E-12] [E-13] [E-14] [E-15]

[E-16] [E-17] [E-18] [E-19] [E-20]

[E-21] [E-22] [E-23] [E-24] [E-25]

[E-21] [E-22] [E-23] [E-24] [E-25]

[E-26] [E-27] [E-28] [E-29] [E-30]

[E-31] [E-32] [E-33] [E-34] [E-35]

[E-31] [E-32] [E-33] [E-34] [E-35]

[E-36] [E-37] [E-38] [E-39] [E-40]

[E-41] [E-42] [E-43] [E-44] [E-45]

[E-46] [E-47] [E-48] [E-49] [E-50]

[E-51] [E-52] [E-53] [E-54] [E-55]

[E-51] [E-52] [E-53] [E-54] [E-55]

[E-56] [E-57] [E-58] [E-59] [E-60]

[E-56] [E-57] [E-58] [E-59] [E-60]

[E-61] [E-62] [E-63] [E-64] [E-65]

[E-61] [E-62] [E-63] [E-64] [E-65]

[E-66] [E-67] [E-68] [E-69] [E-70]

[E-71] [E-72] [E-73] [E-74] [E-75]

[E-71] [E-72] [E-73] [E-74] [E-75]

[E-76] [E-77] [E-78] [E-79] [E-80]

[E-76] [E-77] [E-78] [E-79] [E-80]

[E-81] [E-82] [E-83] [E-84] [E-85]

[E-81] [E-82] [E-83] [E-84] [E-85]

[E-86] [E-87] [E-88] [E-89] [E-90]

[E-86] [E-87] [E-88] [E-89] [E-90]

[E-91] [E-92] [E-93] [E-94] [E-95]

[E-96] [E-97] [E-98] [E-99] [E-100]

[E-101] [E-102] [E-103] [E-104] [E-105]

[E-101] [E-102] [E-103] [E-104] [E-105]

[E-106] [E-107] [E-108] [E-109] [E-110]

[E-106] [E-107] [E-108] [E-109] [E-110]

[E-111] [E-112] [E-113] [E-114] [E-115]

[E-111] [E-112] [E-113] [E-114] [E-115]

[E-116] [E-117] [E-118] [E-119] [E-120]

[E-116] [E-117] [E-118] [E-119] [E-120]

[E-121] [E-122] [E-123] [E-124] [E-125]

[E-121] [E-122] [E-123] [E-124] [E-125]

[E-126] [E-127] [E-128] [E-129] [E-130]

[E-126] [E-127] [E-128] [E-129] [E-130]

[E-131] [E-132] [E-133] [E-134] [E-135]

[E-131] [E-132] [E-133] [E-134] [E-135]

[E-136] [E-137] [E-138]

For example, the second organic compound may be an indolocarbazole compound represented by a combination of Formulas 4B-1 and 4B-2 below.

[Formula 4B-1] [Formula 4B-2]

In Formulas 4B-1 and 4B-2,

Y ¹ and Y ³ may each independently be a single bond, a substituted or unsubstituted C6 to C30 arylene group, a divalent substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,

A ¹ and A ³ may each independently be a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,

Two adjacent * in formula 4B-1 combines with two * in formula 4B-2,

The remaining two * in Formula 4B-1 are each independently CR ¹¹ , wherein R ¹¹ are the same as or different from each other,

R ⁹ to R ¹¹ , R ¹⁸ and R ¹⁹ are each Independently, it may be hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof.

^{For example, Y 1} and Y ³ in Formulas 4B-1 and 4B-2 may each independently be a single bond, a substituted or unsubstituted phenylene group, or a substituted or unsubstituted biphenylene group.

^{For example, A 1} and A ³ in Formulas 4B-1 and 4B-2 may be substituted or unsubstituted C6 to C30 aryl groups, for example, the aryl group may be a phenyl group, a biphenyl group, a naphthyl group, a terphenyl group, or an anthracenyl group. And more preferably a biphenyl group, a naphthyl group, a terphenyl group, or a phenyl group. ^{In addition, A 1} and A ³ in Formulas 4B-1 and 4B-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, or a substituted or unsubstituted triphenylene group, a substituted or unsubstituted pyridinyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted dibenzofuranyl group, It may be a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted fluorenyl group, or a combination thereof.

For example, the indolocarbazole compound represented by a combination of Formulas 4B-1 and 4B-2 may be represented by any one of Formulas 4B-a to 4B-e below.

[Formula 4B-a] [Formula 4B-b] [Formula 4B-c]

[Formula 4B-d] [Formula 4B-e]

In Formulas 4B-a to 4B-e, Y ¹ , Y ³ , A ¹ , A ³ , R ⁹ to R ¹¹ , R ¹⁸ and R ¹⁹ are as described above.

For example, the indolocarbazole compound represented by the combination of Formulas 4B-1 and 4B-2 may be Formula 4B-c or 4B-d below.

For example, the indolocarbazole compound represented by the combination of Formulas 4B-1 and 4B-2 may be Formula 4B-c below.

For example, the compound represented by the combination of Formulas 4B-1 and 4B-2 may be, for example, one of the compounds listed in Group 5, but is not limited thereto.

[Group 5]

[F-1] [F-2] [F-3] [F-4] [F-5]

[F-6] [F-7] [F-8] [F-9] [F-10]

[F-11] [F-12] [F-13] [F-14] [F-15]

[F-16] [F-17] [F-18] [F-19] [F-20]

[F-21] [F-22] [F-23] [F-24] [F-25]

[F-26] [F-27] [F-28] [F-29] [F-30]

[F-31] [F-32] [F-33] [F-34] [F-35]

[F-36] [F-37] [F-38] [F-39] [F-40]

[F-41] [F-42] [F-43] [F-44] [F-45]

[F-46] [F-47] [F-48] [F-49] [F-50]

[F-51] [F-52] [F-53] [F-54] [F-55]

[F-56] [F-57] [F-58] [F-59] [F-60]

[F-61] [F-62] [F-63] [F-64] [F-65]

[F-66] [F-67] [F-68] [F-69] [F-70]

[F-71] [F-72] [F-73] [F-74] [F-75]

[F-76] [F-77] [F-78] [F-79] [F-80]

[F-81] [F-82] [F-83] [F-84] [F-85]

[F-86] [F-87] [F-88] [F-89] [F-90]

[F-91] [F-92] [F-93] [F-94] [F-95]

[F-96] [F-97] [F-98] [F-99] [F-100]

[F-101] [F-102] [F-103] [F-104] [F-105]

[F-106] [F-107] [F-108] [F-109] [F-110]

[F-111] [F-112]

The first organic compound and the second organic compound may include various compositions by various combinations. The composition may include the first organic compound and the second compound in a weight ratio of about 1:99 to 99:1, such as about 10:90 to 90:10, about 20:80 to 80:20, about 30:70 To 70:30, about 40:60 to 60:40, or about 50:50 by weight.

The composition may further include one or more organic compounds in addition to the first organic compound and the second organic compound.

The composition may further include a dopant. The dopant may be a red, green or blue dopant. The dopant is a material that emits light by mixing in a small amount, and in general, a material such as a metal complex that emits light through multiple excitation that excites in a triplet state or more may be used. The dopant may be, for example, an inorganic, organic, organic-inorganic compound, and may include one or two or more. The dopant may be included in an amount of about 0.1 to 20% by weight based on the total content of the composition.

An example of the dopant may be 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. And organometallic compounds to be included. The phosphorescent dopant may be, for example, a compound represented by Formula Z, but is not limited thereto.

[Formula Z]

L ₂ MX

In Formula Z, M is a metal, and L and X are the same as or different from each other, and are a ligand that forms a complex compound with M.

The 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 and X are, for example, bidentate It can be a ligand.

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

The organic optoelectronic device may be, for example, an organic light-emitting device, an organic photovoltaic device, or an organic solar cell. The organic optoelectronic device may be, for example, an organic light emitting device.

The organic optoelectronic device may include an anode and a cathode facing each other, and an organic layer positioned between the anode and the cathode, and the organic layer may include the aforementioned organic compound or the aforementioned composition.

The organic layer may include an active layer such as a light emitting layer or a light absorbing layer, and the aforementioned organic compound or the aforementioned composition may be included in the active layer.

The organic layer may include an auxiliary layer positioned between the anode and the active layer and/or between the cathode and the active layer, and the aforementioned organic compound or the aforementioned composition may be included in the auxiliary layer.

1 is a cross-sectional view illustrating an example of an organic light emitting device, which is an example of an organic optoelectronic device.

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

The anode 110 may be made of, for example, a conductor having a high work function to facilitate hole injection, and may be made of, for example, a metal, a metal oxide, and/or a conductive polymer. The anode 110 may be a metal such as nickel, platinum, vanadium, chromium, copper, zinc, 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;} Poly(3-methylthiophene), poly(3,4-(ethylene-1,2-dioxy)thiophene) (polyehtylenedioxythiophene: PEDOT), conductive polymers such as polypyrrole and polyaniline, but are limited thereto. It is not.

The cathode 120 may be made of, for example, a conductor having a low work function to facilitate electron injection, and may be made of, for example, a metal, a metal oxide, and/or a conductive polymer. The cathode 120 may be a metal such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin, lead, cesium, barium, or an alloy thereof; A multilayered material such as LiF/Al, LiO ₂ /Al, LiF/Ca, LiF/Al, and BaF ₂ /Ca may be mentioned, but is not limited thereto.

The organic layer 105 may include the above-described organic compound or the above-described composition.

The organic layer 105 may include an emission layer 130.

The emission layer 130 may include the aforementioned organic compound or the aforementioned composition as a host. The emission layer 130 may further include another organic compound as a host. The light emitting layer 130 may further include a dopant, and the dopant may be, for example, a phosphorescent dopant.

The organic layer 105 may further include an auxiliary layer (not shown) positioned between the anode 110 and the emission layer 130 and/or between the cathode 120 and the emission layer 130. The auxiliary layer may be a hole injection layer, a hole transport layer, an electron blocking layer, an electron injection layer, an electron transport layer, a hole blocking layer, or a combination thereof. The auxiliary layer may include the aforementioned organic compound or the aforementioned composition.

2 is a cross-sectional view of an organic light-emitting device according to another embodiment.

Referring to FIG. 2, an organic light emitting diode 200 according to an embodiment includes an anode 110 and a cathode 120 facing each other, and an organic layer 105 positioned between the anode 110 and the cathode 120. Includes.

The organic layer 105 includes an electron auxiliary layer 140 positioned between the emission layer 230 and the cathode 120. The electron auxiliary layer 140 may be, for example, an electron injection layer, an electron transport layer, and/or a hole blocking layer, and may facilitate injection and movement of electrons between the cathode 120 and the emission layer 230.

For example, the above-described organic compound or the above-described composition may be included in the emission layer 230. The emission layer 230 may further include another organic compound as a host. The light emitting layer 230 may further include a dopant, and the dopant may be, for example, a phosphorescent dopant.

As an example, the above-described organic compound may be included in the electron auxiliary layer 140. The electron auxiliary layer 140 may include the aforementioned organic compound alone, may include at least two types of the aforementioned organic compounds, or may include the aforementioned organic compound and other organic compounds by mixing.

In FIG. 2, as the organic layer 105, at least one hole auxiliary layer (not shown) positioned between the anode 110 and the emission layer 230 may be further included.

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

The above-described implementation examples 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 the rights.

Hereinafter, the starting materials and reactants used in the Examples and Synthesis Examples were purchased from Sigma-Aldrich or TCI, or synthesized through a known method, unless otherwise specified.

(Preparation of compound for organic optoelectronic device)

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

(Compound for the first organic optoelectronic device)

Synthesis of intermediates

Synthesis example 1: Synthesis of Intermediate A

[Scheme 1]

Synthesis of Intermediate A-1

In a 3L round flask, add 4-chloro-2-fluorobenzonitrile (100g, 0.64mol), methyl thioglycolate (70.0ml, 0.77mol), and 1.2L of N,N-dimethylformamide to the internal temperature- Reduce the temperature to 5℃. Sodium tert-butoxide (93.67g, 0.96mol) is slowly added, so that the internal temperature does not exceed 0℃. After stirring at room temperature for 2 hours, the reactant is slowly added dropwise to cold water. The resulting solid was stirred at room temperature, filtered and dried to obtain Intermediate A-1. (142.9 g, 92%).

Synthesis of Intermediate A-2

In a 2L round flask, a mixture of intermediate A-1 (140.0g, 0.58mol) and urea (173.9g, 2.90mol) was stirred at 200°C for 2 hours. After cooling the hot reaction mixture to room temperature, it was poured into sodium hydroxide solution, impurities were removed by filtration, and then the reaction product was acidified (HCl, 2N), and the obtained precipitate was dried to obtain an intermediate A-2 (114.17 g, 78%).

Synthesis of Intermediate A

In a 2000 mL round flask, a mixture of intermediate A-2 (114 g, 0.45 mol) and phosphorus oxychloride (1000 mL) was stirred under reflux for 8 hours. The reaction mixture was cooled to room temperature and poured into ice/water with vigorous stirring to form a precipitate. The reaction product obtained therefrom was filtered to obtain Intermediate A (122.8 g, 94%, white solid). The result of elemental analysis of the produced intermediate A is as follows.

calcd. C10H3Cl3N2S: C, 41.48; H, 1.04; Cl, 36.73; N, 9.67; S, 11.07; found: C, 41.48; H, 1.04; Cl, 36.73; N, 9.67; S, 11.07

Synthesis example 2: Synthesis of intermediates B, C, D

[Scheme 2]

Intermediates B, C, and D were synthesized in the same manner as in Synthesis Example 1, except that the starting materials were changed as shown in Scheme 2.

Synthesis example 3: Synthesis of Intermediate E

[Scheme 3]

Synthesis of Intermediate E-1

In a 3L round flask, add 1.3L of 4-chloro-2-hydroxybenzonitrile (100g, 0.65mol), ethyl bromoacetate (130.5g, 0.78mol), and N,N-dimethylformamide to an internal temperature of -5. Lower the temperature to °C. Sodium tert-butoxide (93.88g, 0.98mol) is slowly added, so that the internal temperature does not exceed 0℃. After stirring at room temperature for 2 hours, the reactant is slowly added dropwise to cold water. The resulting solid was stirred at room temperature, filtered and dried to obtain Intermediate E-1. (132.2 g, 90%).

Synthesis of Intermediate E-2 and Intermediate E

Intermediate E was synthesized in the same manner as Intermediate A-2 and Intermediate A of Synthesis Example 1.

Synthesis example 4: Synthesis of intermediates F, G, H

[Scheme 4]

Intermediates F, G, and H were synthesized in the same manner as in Synthesis Example 3, except that the starting materials were changed as in Scheme 4.

Synthesis example 5: Synthesis of Intermediate I

[Scheme 5]

Synthesis of Intermediate I-1

In a 5L flask, intermediate 4-bromo-9H-carbazole 200.0 g (0.8 mol), iodobenzene 248.7 g (1.2 mol), potassium carbonate 168.5 g (1.2 mol), copper iodide 31.0 g (0.2 mol) , 29.3 g (0.2 mol) of 1,10-phenanthroline was added to 2.5 L of N,N-dimethylformamide, and then refluxed for 24 hours under a nitrogen stream. The resulting mixture was added to 4 L of distilled water to filter the crystallized solid, and then washed with water, methanol and hexane. The obtained solid was extracted with water and dichloromethane to remove moisture from the obtained organic layer with magnesium sulfate, concentrated, and purified by column chromatography to convert Intermediate I-1 to a white solid (216.2 g, 83% yield). Got it.

calcd. C27H18ClN3: C, 67.10; H, 3.75; Br, 24.80; N, 4.35; found: C C, 67.12; H, 3.77; Br, 24.78; N, 4.33

Synthesis of Intermediate I-2

In a 5 L flask, intermediate I-1 (216.0 g, 0.7 mol), 4,4,4',4', 5,5,5',5'-octamethyl-2,2'-bi (1,3, 2-dioxaborolane (212.8 g, 0.8 mol), potassium acetate (KOAc, 197.4 g, 2.0 mol) and 1,1'-bis (diphenylphosphino) ferrocene-palladium ( II ) dichloride (21.9 g, 0.03 mol) and tricyclohexylphosphine (45.1 g, 0.2 mol) were added to 3 L of N,N-dimethylformamide and stirred for 12 hours at 130° C. After completion of the reaction, the reaction solution was mixed with water and EA Water was removed from the organic layer obtained by extraction using magnesium sulfate, concentrated, and purified by column chromatography to obtain Intermediate I-2 as a white solid (205.5 g, 83% yield).

calcd. C26H25BN2O2: C, 78.06; H, 6.55; B, 2.93; N, 3.79; O, 8.67; found: C, 78.08; H, 6.57; B, 2.91; N, 3.77; O, 8.67

Synthesis of Intermediate I-3

In a 5 L flask, intermediate I-2 150.0 g (0.4 mol), intermediate 1-bromo-2-nitrobenzene 164.1 g (0.8 mol), potassium carbonate 278.1 g (2.01 mol) tetrakis (triphenylphosphine) palladium ( 0) 23.5 g (0.02 mol) was added to 2 L of 1,4-dioxane and 1 L of water, followed by heating at 90° C. for 16 hours under a nitrogen stream. After removing the reaction solvent, it was dissolved in dichloromethane, filtered through silica gel/celite, and an appropriate amount of the organic solvent was removed, and then recrystallized with methanol to obtain intermediate I-3 as a yellow solid (86.3 g, 58% yield).

calcd. C18H12N2O2: C, 79.11; H, 4.43; N, 7.69; O, 8.78; found: C, 79.13; H, 4.45; N, 7.67; O, 8.76

Synthesis of Intermediate I

Intermediate I-3 (86.0 g, 0.23 mol), triphenyl phosphine in a 1000 ml flask (309.5 g, 1.18 mol) was added to 600 mL of dichlorobenzene, substituted with nitrogen, and stirred at 160°C for 12 hours. After completion of the reaction, the solvent was removed and purified by column chromatography (Hexane) to obtain Intermediate I as a yellow solid (57.3 g, 73% yield).

Calcd. C18H12N2: C, 86.72; H, 4.85; N, 8.43; found: C, 86.70; H, 4.83; N, 8.47

Synthesis of the final compound

Synthesis example 6

[Scheme 6]

Synthesis of Intermediate 1-1

In a 250 mL flask, Intermediate A (10.0 g, 34.1 mmol), 3-biphenyl boronic acid (7.83 g, 34.53 mmol), potassium carbonate (11.93 g, 86.33 mmol) tetrakis (triphenylphosphine) palladium (0) (1.2g, 1.04 mmol) was added to 80 mL of 1,4-dioxane and 40 mL of water, followed by heating at 70° C. for 12 hours under a stream of nitrogen. The organic layer was separated, added to 240 mL of methanol, and the crystallized solid was filtered, dissolved in monochlorobenzene, filtered through silica gel/celite, and an appropriate amount of the organic solvent was removed, and then recrystallized from monochlorobenzene, and Intermediate 1-1 (10.83 g) , 77% yield) was obtained.

Synthesis of Intermediate 1-2

Intermediate 1-1 (10.5g, 25.78 mmol), phenylboronic acid (3.14g, 25.78 mmol), potassium carbonate (8.91g, 64.45 mmol), tetrakis (triphenylphosphine) palladium (0) in a 250 mL flask ) (0.89g, 0.77 mmol) was added to 70 mL of 1,4-dioxane and 35 mL of water, followed by heating at 70° C. for 12 hours under a nitrogen stream. The organic layer was separated, added to 210 mL of methanol, and the crystallized solid was filtered, dissolved in monochlorobenzene, filtered through silica gel/celite, and an appropriate amount of organic solvent was removed, and then recrystallized from monochlorobenzene to obtain Intermediate 1-2 (8.44 g). , 79% yield) was obtained.

Synthesis of compound 2

In a 100 mL flask, intermediate 1-2 (4.0 g, 8.92 mmol), 3-dibenzofuran boronic acid (2.27 g, 10.70 mmol), tris(dibenzylideneacetone) dipalladium 0.15 g (0.27 mmol) and tri 0.33 g of t-butylphosphine (50% in toluene) and cesium carbonate (5.81 g, 17.84 mmol) were added to 60 mL of 1,4-dioxane, followed by heating at 110° C. for 12 hours under a nitrogen stream. The organic layer was added to 120 mL of methanol to filter the crystallized solid, dissolved in monochlorobenzene and filtered through silica gel/celite, and after removing an appropriate amount of the organic solvent, recrystallized from monochlorobenzene to obtain compound 2 (4.10 g, 79%). Yield) was obtained.

calcd. C40H24N2OS: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52; found: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52

Synthesis example 7 to 33

Each of the following final compounds was synthesized in the same manner as in Synthesis Example 5, except that the compounds shown in Table 1 were used as starting materials.

Synthesis example Starting material Final compound Yield
(yield) Of the final product
Physical property data Synthesis Example 7 Intermediate A

화합물 3

Compound 3 4.39g, (78%) calcd. C40H24N2OS: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52; found: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52 Synthesis Example 8 Intermediate A

Compound 7 4.96g, (76%) calcd. C40H24N2S2: C, 80.51; H, 4.05; N, 4.69; S, 10.75; found: C, 80.51; H, 4.05; N, 4.69; S, 10.75 Synthesis Example 9 Intermediate A

Compound 9 6.35g, (74%) calcd. C44H26N2OS: C, 83.78; H, 4.15; N, 4.44; O, 2.54; S, 5.08; found: C, 83.78; H, 4.15; N, 4.44; O, 2.54; S, 5.08 Synthesis Example 10 Intermediate A

Compound 17 4.55g, (78%) calcd. C46H26N2OS: C, 84.38; H, 4.00; N, 4.28; O, 2.44; S, 4.90; found: C, 84.38; H, 4.00; N, 4.28; O, 2.44; S, 4.89 Synthesis Example 11 Intermediate A

Compound 18 3.71 g,
(65%) calcd. C46H28N2OS: C, 84.12; H, 4.30; N, 4.27; O, 2.44; S, 4.88; found: C, 84.12; H, 4.30; N, 4.27; O, 2.44; S, 4.88 Synthesis Example 12 Intermediate A

Compound 19 3.99 g,
(69%) calcd. C44H26N2OS: C, 83.78; H, 4.15; N, 4.44; O, 2.54; S, 5.08; found: C, 83.78; H, 4.15; N, 4.44; O, 2.54; S, 5.08 Synthesis Example 13 Intermediate A

Compound 23 5.62g, (75%) calcd. C46H28N2OS: C, 84.12; H, 4.30; N, 4.27; O, 2.44; S, 4.88; found: C, 84.12; H, 4.30; N, 4.27; O, 2.44; S, 4.88 Synthesis Example 14 Intermediate A

Compound 26 4.84g, (73%) calcd. C40H24N2OS: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52; found: C, 82.73; H, 4.17; N, 4.81; O, 2.76; S, 5.52 Synthesis Example 15 Intermediate A

Compound 27 5.04g, (78%) calcd. C40H24N2OS: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52; found: C, 82.72; H, 4.17; N, 4.82; O, 2.76; S, 5.52 Synthesis Example 16 Intermediate A

Compound 34 5.27g, (80%) calcd. C46H28N2OS: C, 84.12; H, 4.30; N, 4.27; O, 2.44; S, 4.88; found: C, 84.11; H, 4.30; N, 4.27; O, 2.44; S, 4.88 Synthesis Example 17 Intermediate B

Compound 38 4.80g, (74%) calcd. C40H24N2OS: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52; found: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52 Synthesis Example 18 Intermediate B

Compound 41 4.06g, (75%) calcd. C40H24N2OS: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52; found: C, 82.72; H, 4.17; N, 4.81; O, 2.77; S, 5.52 Synthesis Example 19 Intermediate B

Compound 43 6.78g, (75%) calcd. C40H24N2OS: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52; found: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52 Synthesis Example 20 Intermediate D

Compound 69 4.83g, (72%) calcd. C40H24N2OS: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52; found: C, 82.71; H, 4.17; N, 4.82; O, 2.76; S, 5.52 Synthesis Example 21 Intermediate D

Compound 70 4.56g, (76%) calcd. C40H24N2OS: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52; found: C, 82.70; H, 4.17; N, 4.82; O, 2.76; S, 5.52 Synthesis Example 22 Intermediate D

Compound 76 4.36g, (72%) calcd. C40H24N2OS: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52; found: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52 Synthesis Example 23 Intermediate C

Compound 97 7.20g, (78%) calcd. C40H24N2OS: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52; found: C, 82.73; H, 4.17; N, 4.82; O, 2.76; S, 5.52 Synthesis Example 24 Intermediate C

Compound 114 6.11g, (75%) calcd. C46H28N2OS: C, 84.12; H, 4.30; N, 4.27; O, 2.44; S, 4.88; found: C, 84.12; H, 4.30; N, 4.27; O, 2.44; S, 4.88 Synthesis Example 25 Intermediate E

Compound 131 4.62g, (70%) calcd. C40H24N2O2: C, 85.09; H, 4.28; N, 4.96; O, 5.67; found: C, 85.09; H, 4.28; N, 4.96; O, 5.67 Synthesis Example 26 Intermediate E

Compound 145 4.90g, (75%) calcd. C46H26N2O2: C, 86.50; H, 4.10; N, 4.39; O, 5.01; found: C, 86.50; H, 4.10; N, 4.39; O, 5.01 Synthesis Example 27 Intermediate E

Compound 154 4.55g, (78%) calcd. C40H24N2O2: C, 85.09; H, 4.28; N, 4.96; O, 5.67; found: C, 85.09; H, 4.27; N, 4.96; O, 5.67 Synthesis Example 28 Intermediate F

Compound 168 4.52g, (71%) calcd. C46H28N2O2: C, 86.23; H, 4.40; N, 4.37; O, 4.99; found: C, 86.23; H, 4.40; N, 4.37; O, 4.99 Synthesis Example 29 Intermediate F

Compound 169 4.28g, (76%) calcd. C40H24N2O2: C, 85.09; H, 4.28; N, 4.96; O, 5.67; found: C, 85.09; H, 4.27; N, 4.96; O, 5.67 Synthesis Example 30 Intermediate H

Compound 199 4.01g, (69%) calcd. C40H24N2O2: C, 85.09; H, 4.28; N, 4.96; O, 5.67; found: C, 85.09; H, 4.27; N, 4.96; O, 5.67 Synthesis Example 31 Intermediate H

Compound 206 4.57g, (74%) calcd. C46H28N2O2: C, 86.23; H, 4.40; N, 4.37; O, 4.99; found: C, 86.23; H, 4.40; N, 4.37; O, 4.99 Synthesis Example 32 Intermediate G

Compound 225 4.69g, (75%) calcd. C40H24N2O2: C, 85.09; H, 4.28; N, 4.96; O, 5.67; found: C, 85.09; H, 4.27; N, 4.96; O, 5.67 Synthesis Example 33 Intermediate G

Compound 256 4.94g, (78%) calcd. C44H26N2O2: C, 85.97; H, 4.26; N, 4.56; O, 5.21; found: C, 85.97; H, 4.26; N, 4.56; O, 5.20

(2nd organic optoelectronic device compound)

Synthesis example 34

[Scheme 8]

Synthesis of Intermediate B2

In a 1000 mL round flask, indolocarbazole 39.99 g (156.01 mmol), bromobenzene 26.94 g (171.61 mmol), sodium t-butoxide 22.49 g (234.01 mmol), tris(dibenzylideneacetone)dipalladium 4.28 g (4.68 mmol) and 2.9 mL of tri t-butylphosphine (50% in toluene) were mixed with 500 mL of xylene, and heated under a nitrogen stream for 15 hours to reflux. The resulting mixture was added to 1000 mL of methanol, and the crystallized solid was filtered, dissolved in dichlorobenzene, filtered through silica gel/celite, and an appropriate amount of organic solvent was removed, and then recrystallized with methanol to obtain intermediate B2 (23.01 g, 44). % Yield) was obtained.

calcd. C ₂₄ H ₁₆ N ₂ : C, 86.72; H, 4.85; N, 8.43; found: C, 86.72; H, 4.85; N, 8.43

Synthesis of compound F-21

In a 500 mL round flask, intermediate B2 22.93 g (69.03 mmol), bromobenzene 11.38 g (72.49 mmol), potassium hydroxide 4.26 g (75.94 mmol), carpaiodide 13.14 g (69.03 mmol), 1,10- 6.22 g (34.52 mmol) of phenanthroline was added to 230 mL of DMF and heated for 15 hours under a nitrogen stream to reflux. The resulting mixture was added to 1000 mL of methanol, and the crystallized solid was filtered, dissolved in dichlorobenzene, filtered through silica gel/celite, and an appropriate amount of the organic solvent was removed, and then recrystallized with methanol to obtain compound F-21 (12.04 g). , 43% yield) was obtained.

calcd. C ₃₀ H ₂₀ N ₂ : C, 88.21; H, 4.93; N, 6.86; found: C, 88.21; H, 4.93; N, 6.86

Synthesis example 35 to 47

Each of the following final compounds was synthesized in the same manner as in Synthesis Example 34, except that the compounds shown in Table 2 were used as starting materials.

Synthesis example Starting material Final product Yield
(yield) Of the final product
Physical property data Synthesis Example 35

Compound F-23 10.23g, (45%) calcd. C42H28N2: C, 89.97; H, 5.03; N, 5.00; found: C, 89.97; H, 5.03; N, 5.00 Synthesis Example 36 Intermediate I

Compound F-41 7.31g, (77%) calcd. C30H20N2: C, 88.21; H, 4.93; N, 6.86; found: C, 88.21; H, 4.93; N, 6.86 Synthesis Example 37

Compound F-43 6.33g, (76%) calcd. C42H28N2: C, 89.97; H, 5.03; N, 5.00; found: C, 89.97; H, 5.03; N, 5.00 Synthesis Example 38

Compound F-73 8.33g, (74%) calcd. C42H28N2: C, 89.97; H, 5.03; N, 5.00; found: C, 89.97; H, 5.03; N, 5.00 Synthesis Example 39

Compound F-99 5.53g, (79%) calcd. C42H28N2: C, 89.97; H, 5.03; N, 5.00; found: C, 89.97; H, 5.03; N, 5.00 Synthesis Example 40

Compound F-100 7.41 g,
(73%) calcd. C42H28N2: C, 89.97; H, 5.03; N, 5.00; found: C, 89.97; H, 5.03; N, 5.00 Synthesis Example 41

Compound F-102 5.94 g,
(76%) calcd. C46H30N2: C, 90.46; H, 4.95; N, 4.59; found: C, 90.46; H, 4.95; N, 4.59 Synthesis Example 42

Compound F-103 6.37 g,
(76%) calcd. C46H30N2: C, 90.46; H, 4.95; N, 4.59; found: C, 90.46; H, 4.95; N, 4.59 Synthesis Example 43

Compound F-104 10.39 g,
(79%) calcd. C46H30N2: C, 90.46; H, 4.95; N, 4.59; found: C, 90.46; H, 4.95; N, 4.59 Synthesis Example 44 Intermediate I

Compound F-105 5.33 g,
(69%) calcd. C46H30N2: C, 90.46; H, 4.95; N, 4.59; found: C, 90.46; H, 4.95; N, 4.59 Synthesis Example 45

Compound F-106 6.96 g,
(77%) calcd. C46H30N2: C, 90.46; H, 4.95; N, 4.59; found: C, 90.46; H, 4.95; N, 4.59 Synthesis Example 46

Compound F-107 6.11 g,
(77%) calcd. C40H26N2: C, 89.86; H, 4.90; N, 5.24; found: C, 89.86; H, 4.90; N, 5.24 Synthesis Example 47 Intermediate I

Compound F-110 9.44 g,
(75%) calcd. C46H30N2: C, 90.46; H, 4.95; N, 4.59; found: C, 90.46; H, 4.95; N, 4.59

Fabrication of organic light emitting device I

Example One

The glass substrate on which the ITO electrode was formed was cut into a size of 50 mm x 50 mm x 0.5 mm, ultrasonically cleaned in acetone isopropyl alcohol and pure water for 15 minutes, and then UV ozone cleaned for 30 minutes.

M-MTDATA on the ITO electrode was vacuum-deposited at a deposition rate of 1 Å/sec to form a 600 Å-thick hole injection layer, and the α-NPB was vacuum deposited on the hole injection layer at a deposition rate of 1 Å/sec to a thickness of 300 Å. A hole transport layer of was formed. Subsequently, on the hole transport layer, Ir(ppy) ₃ (dopant 1) and compound 2 (host) were co-deposited at a deposition rate of 0.1 Å/sec and 1 Å/sec, respectively, to form a light emitting layer having a thickness of 400 Å. BAlq was vacuum deposited on the emission layer at a deposition rate of 1 Å/sec to form a hole blocking layer having a thickness of 50 Å, and then Alq ₃ was vacuum deposited on the hole blocking layer to form an electron transport layer having a thickness of 300 Å. LiF 10Å (electron injection layer) and Al 2000Å (cathode) were sequentially vacuum deposited on the electron transport layer to fabricate an organic light-emitting device.

Example 2 to 25

An organic light-emitting device was manufactured in the same manner as in Example 1, except that the compounds shown in Table 1 were used instead of compound 2 as the emission layer host.

Comparative example 1 to 5

An organic light-emitting device was manufactured in the same manner as in Example 1, except that Comparative Compounds 18, 40, 48, 155, or 189 was used instead of Compound 2 as the emission layer host.

Comparative compounds 18, 40, 48, 155, or 189 were prepared by the method disclosed in JP Patent No. 56,04848 or JP Patent Publication No. 2015-134745.

Evaluation example I

Power is supplied from a current voltmeter (Kethley SMU 236) to the driving voltage, efficiency, and luminance of the organic light emitting devices according to Examples 1 to 25 and Comparative Examples 1 to 5, and the luminance meter PR650 Spectroscan Source Measurement Unit. Lim) was evaluated using.

The specific measurement method is as follows.

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

For the prepared organic light-emitting device, while increasing the voltage from 0V to 10V, a current-voltmeter (Keithley 2400) was used to measure the current value flowing through the unit device, and the measured current value was divided by the area to obtain a result.

(2) Measurement of luminance change according to voltage change

For the prepared 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

The current efficiency (cd/A) of the same current density (10 mA/cm2) was calculated using the luminance, current density, and voltage measured from the above (1) and (2).

(4) Life measurement

The T ₉₅ lifetime is an evaluation of the time (hr) it takes to achieve a luminance of 95% compared to 100% of the initial luminance.

The results are shown in Table 3.

Yes Host Dopant Driving voltage
(V) Current efficiency
(cd/A) Luminance
(cd/m ² ) T ₉₅ life
(hr) Example 1 Compound 2 Dopant 1 4.5 45 6000 77 Example 2 Compound 3 Dopant 1 4.4 44 6000 80 Example 3 Compound 7 Dopant 1 4.7 39 6000 73 Example 4 Compound 17 Dopant 1 4.4 43 6000 76 Example 5 Compound 18 Dopant 1 4.3 45 6000 81 Example 6 Compound 23 Dopant 1 4.6 44 6000 76 Example 7 Compound 26 Dopant 1 4.6 46 6000 80 Example 8 Compound 27 Dopant 1 4.5 45 6000 81 Example 9 Compound 34 Dopant 1 4.5 46 6000 80 Example 10 Compound 38 Dopant 1 4.6 44 6000 76 Example 11 Compound 41 Dopant 1 4.4 45 6000 79 Example 12 Compound 43 Dopant 1 4.5 44 6000 79 Example 13 Compound 69 Dopant 1 4.4 46 6000 81 Example 14 Compound 70 Dopant 1 4.6 45 6000 79 Example 15 Compound 76 Dopant 1 4.4 45 6000 80 Example 16 Compound 97 Dopant 1 4.7 42 6000 75 Example 17 Compound 114 Dopant 1 4.8 43 6000 74 Example 18 Compound 131 Dopant 1 4.3 46 6000 72 Example 19 Compound 145 Dopant 1 4.4 47 6000 73 Example 20 Compound 154 Dopant 1 4.5 45 6000 70 Example 21 Compound 168 Dopant 1 4.4 44 6000 67 Example 22 Compound 169 Dopant 1 4.3 44 6000 68 Example 23 Compound 199 Dopant 1 4.5 45 6000 67 Example 24 Compound 206 Dopant 1 4.3 46 6000 69 Example 25 Compound 225 Dopant 1 4.4 45 6000 70 Comparative Example 1 Comparative compound 18 Dopant 1 6.0 35 6000 38 Comparative Example 2 Comparative compound 40 Dopant 1 4.4 37 6000 34 Comparative Example 3 Comparative compound 48 Dopant 1 4.3 38 6000 30 Comparative Example 4 Comparative compound 156 Dopant 1 4.6 36 6000 23 Comparative Example 5 Comparative compound 189 Dopant 1 4.9 35 6000 39

From Table 3, it can be seen that the organic light-emitting devices according to Examples 1 to 25 have equal to low driving voltage, high efficiency, and/or long life compared to the organic light-emitting devices according to Comparative Examples 1 to 5. Accordingly, the host used in the light emitting layer of the organic light emitting device according to Examples 1 to 25 is a phosphorescent host material and has excellent charge transport properties, and the absorption spectrum of the dopant and the emission wavelength region overlap, from which the efficiency is equal to or It can be seen that the performance as an OLED material is improved and the ability as an OLED material is maximized. Above all, it can be seen that the lifespan is significantly improved.

On the other hand, Comparative Compound 18 used as a host in the organic light emitting device according to Comparative Example 1 had an excessively weak electron transport ability, so it was difficult to achieve a balance between hole transport and electron transport. Accordingly, Comparative Example 1 used it as a host of the light emitting layer. Accordingly, it can be seen that the current efficiency of the organic light emitting device is poor. In addition, Comparative Compounds 18, 40, 48, and 156 used as hosts in the organic light-emitting device according to Comparative Examples 2 to 5 are a structure in which carbon adjacent to N of pyridine, pyrimidine, and quinoxaline in the fused ring is unsubstituted, that is As a structure having CH, in this case, the thermal stability and electrical stability of the light-emitting layer of the organic light-emitting device to which it is applied may be weak, and accordingly, it can be confirmed that the lifetime characteristics of the organic light-emitting device according to the comparative example using it as a host of the light-emitting layer are significantly low. have.

Fabrication of organic light emitting device II

Example 26

Compound 3 obtained in Synthesis Example 7 was used as a host, and (piq) ₂ Ir(acac) (dopant 2) was used as a dopant to fabricate an organic light-emitting device.

ITO was used with a thickness of 1000 Å as the anode, and aluminum (Al) was used with a thickness of 1000 Å as the cathode. Specifically, when explaining the manufacturing method of the organic light-emitting device, the anode ^{cuts an ITO glass substrate having a sheet resistance of 15 Ω/cm 2} into a size of 50 mm ⅹ 50 mm ⅹ 0.7 mm, and each 15 in acetone, isopropyl alcohol and pure water. After ultrasonic cleaning for minutes, UV ozone cleaning was used for 30 minutes.

N4,N4'-di(naphthalen-1-yl)-N4,N4'-diphenylbiphenyl-4,4 under conditions of a vacuum degree of 650 x 10 ^{-7 Pa on the substrate and a deposition rate of 0.1 to 0.3 nm/s} A hole transport layer of 800Å was formed by depositing'-diamine (N4,N4'-di(naphthalene-1-yl)-N4,N4'-diphenylbiphenyl-4,4'-diamine:NPB) (80nm). Subsequently, a light emitting layer having a thickness of 300 Å was formed using the compound 3 obtained in Synthesis Example 7 under the same vacuum deposition conditions, and at this time, a phosphorescent dopant (piq) ₂ Ir (acac) was simultaneously deposited. At this time, the deposition rate of the phosphorescent dopant was adjusted so that when the total amount of the light emitting layer was 100% by weight, the amount of the phosphorescent dopant was 3% by weight.

Bis(2-methyl-8-quinolinolate)-4-(phenylphenolato) aluminum (bis(2-methyl-8-quinolinolate)-4-(phenylphenolato) aluminum: BAlq) was deposited to form a hole blocking layer having a thickness of 50Å. Subsequently, Alq3 was deposited under the same vacuum deposition conditions to form an electron transport layer having a thickness of 200 Å. An organic optoelectronic device was fabricated by sequentially depositing LiF and Al as cathodes on the electron transport layer.

The structure of the organic optoelectronic device is ITO/ NPB (80 nm)/ EML (Compound 3 (97% by weight) + (piq) ₂ Ir(acac) (3% by weight), 30 nm)/ Balq (5 nm)/ Alq3 (20 nm )/ LiF (1 nm) / Al (100 nm).

Example 27 to Example 35

An organic light-emitting device was manufactured in the same manner as in Example 26, except that Compounds 9, 17, 18, 19, 23, 41, 97, 131, and 256 were used instead of Compound 3 as a host when forming the emission layer.

Comparative example 6 to 13

An organic light-emitting device was manufactured in the same manner as in Example 52, except that Comparative Compounds 18, 40, 48, 155, 156, 189, 327, and 328 were used, respectively, instead of Compound 3 as the emission layer host.

Comparative compounds 18, 40, 48, 155, or 189 were prepared by the method disclosed in JP Patent No. 56,04848 or JP Patent Publication No. 2015-134745.

Evaluation example II

The luminous efficiency and lifetime characteristics of the organic light emitting devices according to Examples 26 to 35 and Comparative Examples 6 to 13 were evaluated.

Specific measurement methods are as follows, and the results are shown in Table 4.

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

For the prepared organic light-emitting device, while increasing the voltage from 0V to 10V, a current-voltmeter (Keithley 2400) was used to measure the current value flowing through the unit device, and the measured current value was divided by the area to obtain a result.

(2) Measurement of luminance change according to voltage change

For the prepared 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

The current efficiency (cd/A) of the same current density (10 mA/cm2) was calculated using the luminance, current density, and voltage measured from the above (1) and (2).

(4) Life measurement

The luminance (cd/m2) was maintained at 5000 cd/m2 and the time at which the current efficiency (cd/A) decreased to 90% was measured to obtain a result.

(5) Roll-off

Among the characteristic values of (3), (Max value-the value at 5000 cd/m ² / Max value) was calculated, and the drop width of the efficiency was calculated as %.

Host Dopant Driving
Voltage
(V) radiation
efficiency
(cd/A) Roll-off
(%) Life T90
(h) Example 26 Compound 3 Dopant 2 4.66 14.3 15.5 125 Example 27 Compound 9 Dopant 2 4.50 15.2 14.8 131 Example 28 Compound 17 Dopant 2 4.60 14.4 15.0 133 Example 29 Compound 18 Dopant 2 4.32 14.5 14.1 142 Example 30 Compound 19 Dopant 2 4.23 14.2 14.4 140 Example 31 Compound 23 Dopant 2 4.19 14.8 14.5 139 Example 32 Compound 41 Dopant 2 4.42 14.0 15.4 133 Example 33 Compound 97 Dopant 2 4.48 14.6 15.6 135 Example 34 Compound 131 Dopant 2 4.43 14.7 14.3 119 Example 35 Compound 256 Dopant 2 4.31 14.8 14.9 118 Comparative Example 6 Comparative compound 18 Dopant 2 5.51 13.4 13.0 85 Comparative Example 7 Comparative compound 40 Dopant 2 4.44 13.9 16.9 64 Comparative Example 8 Comparative compound 48 Dopant 2 4.50 14.0 15.1 60 Comparative Example 9 Comparative compound 155 Dopant 2 4.47 14.1 13.8 52 Comparative Example 10 Comparative compound 156 Dopant 2 4.50 13.5 14.3 58 Comparative Example 11 Comparative compound 189 Dopant 2 4.66 14.1 14.9 63 Comparative Example 12 Comparative compound 327 Dopant 2 5.14 13.2 13.0 89 Comparative Example 13 Comparative compound 328 Dopant 2 5.20 13.8 14.2 82

Referring to Table 4, the organic light-emitting device of Examples 26 to 35 of the present invention has an excellent long life in terms of equal or low driving voltage, equivalent or excellent luminous efficiency compared to the organic light-emitting device according to Comparative Examples 6 to 13 can confirm.

Accordingly, the host used in the emission layer of the organic light-emitting device according to Examples 26 to 35 is a phosphorescent host material and has excellent charge transport characteristics, and the absorption spectrum of the dopant and the emission wavelength region overlap, thereby increasing efficiency and driving voltage. It can be seen that the reduction of and, in particular, the improvement of performance such as long life and the ability as an OLED material is maximized.

Fabrication of organic light emitting device III

Example 36 to 60 and Comparative example 14 to 21

An organic light-emitting device was manufactured in the same manner as in Example 1, except that the first host and the second host shown in Table 6 were used instead of the compound 2 as the host of the emission layer. At this time, the dopant: the first host: the second host was co-deposited at a weight ratio of 10:45:45.

Evaluation example III

By supplying power from a current voltmeter (Kethley SMU 236) for the driving voltage, efficiency, luminance, and lifetime of the organic light emitting devices of Examples 36 to 60 and Comparative Examples 14 to 21, the luminance PR650 Spectroscan Source Measurement Unit. Im) is shown in Table 5 below. The T ₉₅ lifetime is an evaluation of the time (hr) it takes to achieve a luminance of 95% compared to 100% of the initial luminance.

Example Host 1 2nd host Dopant Driving
Voltage
(V) Current efficiency
(cd/A) Luminance
(cd/m ² ) T ₉₅
life span
(hr) 36 Compound 2 E-31 Dopant 1 4.3 47 6000 85 37 Compound 3 E-31 Dopant 1 4.1 48 6000 87 38 Compound 18 E-31 Dopant 1 4.0 47 6000 87 39 Compound 34 E-31 Dopant 1 4.2 47 6000 84 40 Compound 69 E-31 Dopant 1 4.3 46 6000 84 41 Compound 76 E-31 Dopant 1 4.2 46 6000 85 42 Compound 131 E-31 Dopant 1 4.0 48 6000 80 43 Compound 199 E-31 Dopant 1 4.1 46 6000 77 44 Compound 2 E-99 Dopant 1 4.2 48 6000 83 45 Compound 3 E-99 Dopant 1 3.9 48 6000 85 46 Compound 18 E-99 Dopant 1 3.9 47 6000 86 47 Compound 34 E-99 Dopant 1 3.9 47 6000 83 48 Compound 69 E-99 Dopant 1 4.1 45 6000 83 49 Compound 76 E-99 Dopant 1 4.1 45 6000 85 50 Compound 131 E-99 Dopant 1 3.9 46 6000 79 51 Compound 2 F-43 Dopant 1 3.9 47 6000 82 52 Compound 3 F-43 Dopant 1 3.7 47 6000 83 53 Compound 18 F-43 Dopant 1 3.7 46 6000 84 54 Compound 76 F-43 Dopant 1 3.9 45 6000 83 55 Compound 2 F-99 Dopant 1 4.0 48 6000 82 56 Compound 3 F-99 Dopant 1 3.7 48 6000 84 57 Compound 18 F-99 Dopant 1 3.8 46 6000 84 58 Compound 76 F-99 Dopant 1 3.9 46 6000 82 59 Compound 2 F-73 Dopant 1 4.4 47 6000 83 60 Compound 3 F-73 Dopant 1 4.3 47 6000 85 Comparative Example 14 Comparative compound 18 E-31 Dopant 1 5.5 38 6000 49 Comparative Example 15 Comparative compound 40 E-31 Dopant 1 4.3 42 6000 43 Comparative Example 16 Comparative compound 48 E-31 Dopant 1 4.1 41 6000 40 Comparative Example 17 Comparative compound 189 E-31 Dopant 1 4.3 39 6000 35 Comparative Example 18 Comparative compound 18 E-43 Dopant 1 5.2 34 6000 46 Comparative Example 19 Comparative compound 40 E-43 Dopant 1 4.1 40 6000 41 Comparative Example 20 Comparative compound 48 E-43 Dopant 1 3.9 38 6000 39 Comparative Example 21 Comparative compound 189 E-43 Dopant 1 4.0 38 6000 32

From Table 5, it can be seen that the organic light-emitting devices according to Examples 36 to 60 have improved efficiency and/excellent long life at the same or low driving voltage compared to the organic light-emitting devices according to Comparative Examples 14 to 21.

Fabrication of organic light emitting device IV

Example 61 to 75 and Comparative example 22 to 25

An organic light-emitting device was manufactured in the same manner as in Example 26, except that the first host and the second host shown in Table 7 were used instead of compound 2 as the host of the emission layer. At this time, the dopant: the first host: the second host was co-deposited at a weight ratio of 3:48.5:48.5.

Evaluation example IV

By supplying power from a current voltmeter (Kethley SMU 236) for the driving voltage, efficiency, luminance, and lifetime of the organic light emitting devices according to Examples 61 to 75 and Comparative Examples 22 to 25, the luminance PR650 Spectroscan Source Measurement Unit.(PhotoResearch Co., Ltd.) Product).

The results are shown in Table 6.

First host 2nd host Dopant Driving
Voltage
(V) radiation
efficiency
(cd/A) Life T90
(h) Example 61 Compound 3 E-99 Dopant 2 4.10 17.9 152 Example 62 Compound 3 F-104 Dopant 2 3.91 19.4 181 Example 63 Compound 3 F-106 Dopant 2 3.87 19.7 187 Example 64 Compound 3 F-107 Dopant 2 3.95 18.9 177 Example 65 Compound 3 F-110 Dopant 2 3.97 19.1 180 Example 66 Compound 9 F-104 Dopant 2 3.80 20.3 184 Example 67 Compound 18 F-104 Dopant 2 3.88 19.9 180 Example 68 Compound 19 F-104 Dopant 2 3.91 20.4 179 Example 69 Compound 23 F-104 Dopant 2 3.90 20.3 185 Example 70 Compound 256 F-104 Dopant 2 3.78 20.3 169 Example 71 Compound 9 F-106 Dopant 2 3.78 20.4 190 Example 72 Compound 18 F-106 Dopant 2 3.87 20.2 187 Example 73 Compound 19 F-106 Dopant 2 3.86 20.4 183 Example 74 Compound 23 F-106 Dopant 2 3.89 20.4 189 Example 75 Compound 256 F-106 Dopant 2 3.78 20.2 172 Comparative Example 22 Comparative compound 18 F-106 Dopant 2 4.78 17.3 103 Comparative Example 23 Comparative compound 40 F-106 Dopant 2 4.15 18.0 80 Comparative Example 24 Comparative compound 327 F-106 Dopant 2 4.66 17.9 109 Comparative Example 25 Comparative compound 328 F-106 Dopant 2 4.50 17.6 106

From Table 6, it can be seen that the organic light-emitting devices according to Examples 61 to 75 have a longer life compared to the organic light-emitting devices according to Comparative Examples 22 to 25.

The present invention is not limited to the above embodiments, but may be manufactured in a variety of different forms, and those of ordinary skill in the art to which the present invention pertains, other specific forms without changing the technical spirit or essential features of the present invention. It will be appreciated that it can be implemented with. Therefore, it should be understood that the embodiments described above are illustrative and non-limiting in all respects.

The scope of the present invention is not limited thereto, and various modifications and improvements of those skilled in the art using the basic concept of the present invention defined in the following claims also belong to the scope of the present invention.

100, 200: organic light emitting device
105: organic layer
110: anode
120: cathode
130, 230: light emitting layer
140: electron auxiliary layer

Claims (14)

Organic compound represented by the following formula (1):
[Formula 1]

In Formula 1,
X ¹ and X ² are each independently O or S,
Ar ¹ and Ar ² are each independently a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof, wherein the substitution is at least one hydrogen is deuterium, a C1 to C20 alkyl group, It is substituted with a C6 to C12 aryl group or a cyano group,
L ¹ is a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C6 to C30 arylene group, or a combination thereof,
R ¹ to R ⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heterocyclic group, a cyano group, or these It is a combination of.
In claim 1,
The Ar ¹ and Ar ² are each independently a substituted or unsubstituted C6 to C30 aryl group, wherein the substitution is that at least one hydrogen is substituted with deuterium, a C1 to C20 alkyl group, a C6 to C12 aryl group or a cyano group. Organic compounds.
In paragraph 2,
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, or a substituted or unsubstituted anthracenyl group, A substituted or unsubstituted triphenylene group, wherein the substitution is an organic compound in which at least one hydrogen is substituted with deuterium, a C1 to C20 alkyl group, a C6 to C12 aryl group or a cyano group.
In claim 1,
An organic compound represented by any one of the following formulas 2 to 5:
[Formula 2] [Formula 3]

[Formula 4] [Formula 5]

In Formulas 2 to 5,
X ¹ and X ² are each independently O or S,
Ar ¹ and Ar ² are each independently a C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof, wherein the substitution is at least one hydrogen is deuterium, a C1 to C20 alkyl group, a C6 to C12 aryl group Or substituted with a cyano group,
L ¹ is a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C6 to C30 arylene group, or a combination thereof,
R ¹ to R ⁶ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heterocyclic group, a cyano group, or these It is a combination of.
In claim 1,
Ar ¹ and Ar ² are each independently a C6 to C30 aryl group, wherein the substitution is that at least one hydrogen is substituted with a deuterium, a C1 to C20 alkyl group, a C6 to C12 aryl group or a cyano group,
L ¹ is a single bond or a substituted or unsubstituted phenylene group,
R ¹ to R ⁶ are each independently hydrogen, a cyano group, a C1 to C4 alkyl group, a C6 to C12 aryl group, or a C6 to C12 aryl group substituted with a cyano group.
In claim 1,
An organic compound which is one selected from the compounds listed in Group 1 below.
[Group 1]

A first organic compound according to claim 1, and
A second organic compound containing a carbazole moiety represented by the following formula (4)
Composition comprising:
[Formula 4]

In Chemical Formula 4,
Y ¹ is a single bond, a substituted or unsubstituted C6 to C30 arylene group or a divalent substituted or unsubstituted C2 to C30 heterocyclic group,
A ¹ is a substituted or unsubstituted C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group,
R ⁹ to R ¹⁴ are each Independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heterocyclic group,
R ¹¹ to R ¹⁴ are each They exist independently, or ^{adjacent groups among R 11} to R ¹⁴ are connected to each other to form a ring.
In clause 7,
The second organic compound is a composition represented by the following formula 4A or a combination of the following formulas 4B-1 and 4B-2:
[Formula 4A] [Formula 4B-1] [Formula 4B-2]

In Formula 4A, Formula 4B-1 or Formula 4B-2,
Y ¹ to Y ³ are each independently a single bond, a substituted or unsubstituted C6 to C30 arylene group, a divalent substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,
A ¹ to A ³ are each independently a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,
Two adjacent * in formula 4B-1 combines with two * in formula 4B-2,
The remaining two * in Formula 4B-1 are each independently CR ¹¹ , wherein R ¹¹ are the same as or different from each other,
R ⁹ to R ¹¹ and R ¹⁵ to R ¹⁹ are each Independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,
m is an integer from 0 to 2.
In clause 8,
^{A 1} to A ³ of Formula 4A, Formula 4B-1 and Formula 4B-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 Substituted naphthyl group, substituted or unsubstituted anthracenyl group, or substituted or unsubstituted triphenylene group, substituted or unsubstituted pyridinyl group, substituted or unsubstituted dibenzothiophenyl group, substituted or unsubstituted dibenzo A composition comprising a furanyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted fluorenyl group, or a combination thereof.
In clause 8,
The second organic compound is a composition represented by the following formulas 4A-1, 4B-c or 4B-d:
[Formula 4A-1]

[Formula 4B-c] [Formula 4B-d]

In Formulas 4A-1, 4B-c and 4B-d,
Y ¹ to Y ³ are each independently a single bond, a substituted or unsubstituted C6 to C30 arylene group, a divalent substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,
A ¹ to A ³ 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, or Substituted or unsubstituted triphenylene group, substituted or unsubstituted pyridinyl group, substituted or unsubstituted dibenzothiophenyl group, substituted or unsubstituted dibenzofuranyl group, substituted or unsubstituted carbazolyl group, substituted or An unsubstituted fluorenyl group or a combination thereof,
R ⁹ to R ¹¹ and R ¹⁵ to R ¹⁹ are each Independently, hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof.
Anode and cathode facing each other, and
An organic layer positioned between the anode and the cathode
Including,
The organic layer is an organic optoelectronic device comprising the organic compound according to claim 1 or the composition according to claim 7.
In clause 11,
The organic layer includes a light emitting layer,
The organic compound or the composition is an organic optoelectronic device included as a host of the emission layer.
In clause 11,
The organic layer
A light emitting layer, and
An electron auxiliary layer positioned between the cathode and the light emitting layer
Including,
The electron auxiliary layer is an organic optoelectronic device comprising the organic compound according to claim 1.
A display device including the organic optoelectronic device according to claim 11.

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