KR102222368B1 - Novel compound and organic light emitting device comprising the same - Google Patents

Abstract

The present invention provides a novel compound and an organic light emitting device using the same.

Description

Novel compound and organic light emitting device comprising the same

The present invention relates to a novel compound and an organic light emitting device comprising the same.

In general, the organic light emission phenomenon refers to a phenomenon in which electrical energy is converted into light energy by using an organic material. An organic light-emitting device using the organic light-emitting phenomenon has a wide viewing angle, excellent contrast, and fast response time, and has excellent luminance, driving voltage, and response speed characteristics, and thus many studies are being conducted.

An organic light-emitting device generally has a structure including an anode and a cathode, and an organic material layer between the anode and the cathode. The organic material layer is often made of a multi-layered structure composed of different materials in order to increase the efficiency and stability of the organic light-emitting device.For example, it may be formed of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer, and the like. In the structure of such an organic light emitting device, when a voltage is applied between the two electrodes, holes are injected from the anode and electrons from the cathode are injected into the organic material layer, and excitons are formed when the injected holes and electrons meet. When it falls back to the ground, it glows.

Development of new materials for organic materials used in organic light emitting devices as described above is continuously required.

Korean Patent Publication No. 10-2000-0051826

The present invention relates to a novel compound and an organic light emitting device comprising the same.

The present invention provides a compound represented by the following formula (1):

[Formula 1]

In Formula 1,

a to d are each independently an integer of 0 to 3,

L is a single bond; Substituted or unsubstituted C _6-60 arylene; _{Or substituted or unsubstituted C 2-60} heteroarylene containing any one or more heteroatoms selected from the group consisting of N, O and S,

X is each independently N or C (R ₅ ), provided that at least one of X is N,

Ar ₁ and Ar ₂ are each independently hydrogen; Substituted or unsubstituted C _6-60 aryl; _{Or substituted or unsubstituted C 2-60} heteroaryl containing any one or more heteroatoms selected from the group consisting of N, O and S,

R ₁ to R ₅ are each independently hydrogen; heavy hydrogen; halogen; Cyano; Substituted or unsubstituted C _1-60 alkyl; Substituted or unsubstituted C _1-60 alkoxy; Substituted or unsubstituted C _1-60 thioalkyl; Substituted or unsubstituted C _3-60 cycloalkyl; Substituted or unsubstituted C _6-60 aryl; Or tri(C _1-60 alkyl)silyl.

In addition, the present invention is a first electrode; A second electrode provided to face the first electrode; And one or more organic material layers provided between the first electrode and the second electrode, wherein at least one of the organic material layers includes a compound represented by Formula 1 do.

The compound represented by Chemical Formula 1 may be used as a material for an organic material layer of an organic light-emitting device, and may improve efficiency, low driving voltage, and/or lifetime characteristics in the organic light-emitting device. In particular, the compound represented by Formula 1 may be used as a hole injection, hole transport, hole injection and transport, light emission, electron transport, or electron injection material.

1 shows an example of an organic light-emitting device comprising a substrate 1, an anode 2, a light-emitting layer 3, and a cathode 4.
2 shows a substrate (1), an anode (2), a hole injection layer (5), a hole transport layer (6), an electron blocking layer (7), a light emitting layer (3), an electron transport layer (8), an electron injection layer (9), and An example of an organic light-emitting device made of the cathode 4 is shown.

Hereinafter, it will be described in more detail to aid in understanding the present invention.

The present invention provides a compound represented by Chemical Formula 1.

,

, 또는

는 다른 치환기에 연결되는 결합을 의미한다. In this specification,

,

, or

Means a bond connected to another substituent.

In the present specification, the term "substituted or unsubstituted" refers to deuterium; Halogen group; Nitrile group; Nitro group; Hydroxy group; Carbonyl group; Ester group; Imide group; Amino group; Phosphine oxide group; Alkoxy group; Aryloxy group; Alkyl thioxy group; Arylthioxy group; Alkyl sulfoxy group; Arylsulfoxy group; Silyl group; Boron group; Alkyl group; Cycloalkyl group; Alkenyl group; Aryl group; Aralkyl group; Aralkenyl group; Alkylaryl group; Alkylamine group; Aralkylamine group; Heteroarylamine group; Arylamine group; Arylphosphine group; Or it means substituted or unsubstituted with one or more substituents selected from the group consisting of a heterocyclic group containing one or more of N, O, and S atoms, or substituted or unsubstituted with two or more substituents connected among the above-exemplified substituents. . For example, "a substituent to which two or more substituents are connected" may be a biphenyl group. That is, the biphenyl group may be an aryl group, or may be interpreted as a substituent to which two phenyl groups are connected.

In the present specification, the number of carbon atoms of the carbonyl group is not particularly limited, but is preferably 1 to 40 carbon atoms. Specifically, it may be a compound having the following structure, but is not limited thereto.

In the present specification, the ester group may be substituted with a C1-C25 linear, branched or cyclic alkyl group or an aryl group having 6 to 25 carbon atoms in the oxygen of the ester group. Specifically, it may be a compound of the following structural formula, but is not limited thereto.

.

In the present specification, the number of carbon atoms of the imide group is not particularly limited, but it is preferably 1 to 25 carbon atoms. Specifically, it may be a compound having the following structure, but is not limited thereto.

In the present specification, the silyl group is specifically trimethylsilyl group, triethylsilyl group, t-butyldimethylsilyl group, vinyldimethylsilyl group, propyldimethylsilyl group, triphenylsilyl group, diphenylsilyl group, phenylsilyl group, etc. However, it is not limited thereto.

In the present specification, the boron group specifically includes a trimethyl boron group, a triethyl boron group, a t-butyldimethyl boron group, a triphenyl boron group, a phenyl boron group, and the like, but is not limited thereto.

In the present specification, examples of the halogen group include fluorine, chlorine, bromine or iodine.

In the present specification, the alkyl group may be linear or branched, and the number of carbon atoms is not particularly limited, but is preferably 1 to 40. According to an exemplary embodiment, the alkyl group has 1 to 20 carbon atoms. According to another exemplary embodiment, the alkyl group has 1 to 10 carbon atoms. According to another exemplary embodiment, the alkyl group has 1 to 6 carbon atoms. Specific examples of the alkyl group include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n -Pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl , n-heptyl, 1-methylhexyl, cyclopentylmethyl, cycloheptylmethyl, octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhexyl, 2-propylpentyl, n-nonyl, 2,2 -Dimethylheptyl, 1-ethyl-propyl, 1,1-dimethyl-propyl, isohexyl, 2-methylpentyl, 4-methylhexyl, 5-methylhexyl, and the like, but are not limited thereto.

In the present specification, the alkenyl group may be a linear or branched chain, and the number of carbon atoms is not particularly limited, but is preferably 2 to 40. According to an exemplary embodiment, the alkenyl group has 2 to 20 carbon atoms. According to another exemplary embodiment, the alkenyl group has 2 to 10 carbon atoms. According to another exemplary embodiment, the alkenyl group has 2 to 6 carbon atoms. Specific examples include vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 3-methyl-1- Butenyl, 1,3-butadienyl, allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, 2,2-diphenylvinyl-1-yl, 2-phenyl-2-( Naphthyl-1-yl)vinyl-1-yl, 2,2-bis(diphenyl-1-yl)vinyl-1-yl, stilbenyl group, styrenyl group, and the like, but are not limited thereto.

In the present specification, the cycloalkyl group is not particularly limited, but preferably has 3 to 60 carbon atoms, and according to an exemplary embodiment, the cycloalkyl group has 3 to 30 carbon atoms. According to another exemplary embodiment, the cycloalkyl group has 3 to 20 carbon atoms. According to another exemplary embodiment, the cycloalkyl group has 3 to 6 carbon atoms. Specifically, cyclopropyl, cyclobutyl, cyclopentyl, 3-methylcyclopentyl, 2,3-dimethylcyclopentyl, cyclohexyl, 3-methylcyclohexyl, 4-methylcyclohexyl, 2,3-dimethylcyclohexyl, 3, 4,5-trimethylcyclohexyl, 4-tert-butylcyclohexyl, cycloheptyl, cyclooctyl, and the like, but are not limited thereto.

In the present specification, the aryl group is not particularly limited, but is preferably 6 to 60 carbon atoms, and may be a monocyclic aryl group or a polycyclic aryl group. According to an exemplary embodiment, the aryl group has 6 to 30 carbon atoms. According to an exemplary embodiment, the aryl group has 6 to 20 carbon atoms. The aryl group may be a phenyl group, a biphenyl group, or a terphenyl group, but the monocyclic aryl group is not limited thereto. The polycyclic aryl group may be a naphthyl group, an anthracenyl group, a phenanthryl group, a pyrenyl group, a perylenyl group, a chrysenyl group, a fluorenyl group, and the like, but is not limited thereto.

등이 될 수 있다. 다만, 이에 한정되는 것은 아니다.In the present specification, the fluorenyl group may be substituted, and two substituents may be bonded to each other to form a spiro structure. When the fluorenyl group is substituted,

Can be, etc. However, it is not limited thereto.

In the present specification, the heterocyclic group is a heterocyclic group containing at least one of O, N, P, Si, and S as heterogeneous elements, and the number of carbons is not particularly limited, but is preferably 2 to 60 carbon atoms. Examples of the heterocyclic group include thiophene group, furan group, pyrrole group, imidazole group, thiazole group, oxazole group, oxadiazole group, triazole group, pyridyl group, bipyridyl group, pyrimidyl group, triazine group, acridyl group , Pyridazine group, pyrazinyl group, quinolinyl group, quinazoline group, quinoxalinyl group, phthalazinyl group, pyrido pyrimidinyl group, pyrido pyrazinyl group, pyrazino pyrazinyl group, isoquinoline group, indole group , Carbazole group, benzoxazole group, benzoimidazole group, benzothiazole group, benzocarbazole group, benzothiophene group, dibenzothiophene group, benzofuranyl group, phenanthroline group, isoxazolyl group, thiiadia There are a zolyl group, a phenothiazinyl group, and a dibenzofuranyl group, but are not limited thereto.

In the present specification, the aryl group among the aralkyl group, aralkenyl group, alkylaryl group, and arylamine group is the same as the example of the aryl group described above. In the present specification, the alkyl group among the aralkyl group, the alkylaryl group and the alkylamine group is the same as the example of the aforementioned alkyl group. In the present specification, for heteroaryl among heteroarylamines, the description of the aforementioned heterocyclic group may be applied. In the present specification, the alkenyl group of the aralkenyl group is the same as the example of the alkenyl group described above. In the present specification, the description of the aryl group described above may be applied except that the arylene is a divalent group. In the present specification, the description of the aforementioned heterocyclic group may be applied except that the heteroarylene is a divalent group. In the present specification, the hydrocarbon ring is not a monovalent group, and the description of the aryl group or cycloalkyl group described above may be applied except that the hydrocarbon ring is formed by bonding of two substituents. In the present specification, the heterocycle is not a monovalent group, and the description of the aforementioned heterocyclic group may be applied, except that two substituents are bonded to each other and formed.

In Chemical Formula 1, preferably, Chemical Formula 1 may be the following Chemical Formula 1-1 or 1-2.

[Formula 1-1]

[Formula 1-2]

In Formula 1-1 or 1-2,

Descriptions of a to d, R ₁ to R ₄ , L, X, Ar ₁ and Ar ₂ are as defined above.

In Formula 1, preferably, a, b, c and d may be 0.

In Formula 1, preferably L is a single bond; Phenylene; Biphenyldiyl; Naphthalenediyl; Dimethylfluorenediyl; Dibenzofurandiyl; Dibenzothiophendiyl; Carbazoldiyl; Phenylene-carbazoldiyl; Or it may be phenylene-naphthalenediyl.

Preferably, all of X may be N.

In addition, preferably Ar ₁ and Ar ₂ may each independently be any one selected from the group consisting of the following.

For example, the compound may be selected from the group consisting of the following compounds:

On the other hand, the compound represented by Formula 1 can be prepared by the same manufacturing method as in Scheme 1 below.

[Scheme 1]

In Reaction Scheme 1, T is halogen, preferably bromo, or chloro, and the definition of other substituents is as described above.

Specifically, the compound represented by Formula 1 is prepared by combining starting materials through a Suzuki coupling reaction. Such a Suzuki coupling reaction is preferably carried out in the presence of a palladium catalyst and a base, and the reactor for the Suzuki coupling reaction can be changed as known in the art. The manufacturing method may be more specific in the manufacturing examples to be described later.

In addition, the present invention provides an organic light-emitting device including the compound represented by Formula 1 above. For example, the present invention provides a first electrode; A second electrode provided to face the first electrode; And one or more organic material layers provided between the first electrode and the second electrode, wherein at least one of the organic material layers includes a compound represented by Formula 1 do.

The organic material layer of the organic light emitting device of the present invention may have a single-layer structure, but may have a multilayer structure in which two or more organic material layers are stacked. For example, the organic light emitting device of the present invention may have a structure including a hole injection layer, a hole transport layer, an electron blocking layer, a light emitting layer, an electron transport layer, an electron injection layer, and the like as an organic material layer. However, the structure of the organic light emitting device is not limited thereto and may include a smaller number of organic layers.

In addition, the organic material layer may include a hole injection layer, a hole transport layer, or a layer that simultaneously injects and transports holes, and the hole injection layer, a hole transport layer, or a layer that simultaneously injects and transports holes is represented by Formula 1 above. It may contain a compound to be displayed.

In addition, the organic material layer may include an emission layer, and the emission layer may include a compound represented by Formula 1 above.

In addition, the organic material layer may include an electron transport layer or an electron injection layer, and the electron transport layer or the electron injection layer may include a compound represented by Formula 1 above.

In addition, the electron transport layer, the electron injection layer, or a layer that simultaneously transports electrons and injects electrons may include a compound represented by Formula 1 above.

In addition, the organic material layer may include an emission layer and an electron transport layer, and the electron transport layer may include a compound represented by Formula 1 above.

In addition, the organic light-emitting device according to the present invention may be a normal type organic light-emitting device in which an anode, one or more organic material layers, and a cathode are sequentially stacked on a substrate. In addition, the organic light-emitting device according to the present invention may be an inverted type organic light-emitting device in which a cathode, one or more organic material layers, and an anode are sequentially stacked on a substrate. For example, the structure of an organic light-emitting device according to an embodiment of the present invention is illustrated in FIGS. 1 and 2.

1 shows an example of an organic light-emitting device comprising a substrate 1, an anode 2, a light-emitting layer 3, and a cathode 4. In such a structure, the compound represented by Formula 1 may be included in the emission layer.

2 shows a substrate (1), an anode (2), a hole injection layer (5), a hole transport layer (6), an electron blocking layer (7), a light emitting layer (3), an electron transport layer (8), an electron injection layer (9), and An example of an organic light-emitting device made of the cathode 4 is shown. In such a structure, the compound represented by Formula 1 may be included in one or more of the hole injection layer, hole transport layer, electron blocking layer, light emitting layer, electron transport layer, and electron injection layer, and preferably included in the light emitting layer. have.

The organic light-emitting device according to the present invention may be manufactured by materials and methods known in the art, except that at least one of the organic material layers includes the compound represented by Chemical Formula 1. In addition, when the organic light-emitting device includes a plurality of organic material layers, the organic material layers may be formed of the same material or different materials.

For example, the organic light emitting device according to the present invention may be manufactured by sequentially stacking a first electrode, an organic material layer, and a second electrode on a substrate. At this time, using a PVD (physical vapor deposition) method such as sputtering or e-beam evaporation, the anode is formed by depositing a metal or a conductive metal oxide or an alloy thereof on the substrate. And, after forming an organic material layer including a hole injection layer, a hole transport layer, a light emitting layer, and an electron transport layer thereon, it can be prepared by depositing a material that can be used as a cathode thereon. In addition to this method, an organic light-emitting device may be manufactured by sequentially depositing a cathode material, an organic material layer, and an anode material on a substrate.

In addition, the compound represented by Formula 1 may be formed as an organic material layer by a solution coating method as well as a vacuum deposition method when manufacturing an organic light emitting device. Here, the solution coating method refers to spin coating, dip coating, doctor blading, inkjet printing, screen printing, spray method, roll coating, and the like, but is not limited thereto.

In addition to such a method, an organic light emitting device may be manufactured by sequentially depositing an organic material layer and an anode material from a cathode material on a substrate (WO 2003/012890). However, the manufacturing method is not limited thereto.

For example, the first electrode is an anode, the second electrode is a cathode, or the first electrode is a cathode, and the second electrode is an anode.

As the anode material, a material having a large work function is preferable so that holes can be smoothly injected into the organic material layer. Specific examples of the cathode material include metals such as vanadium, chromium, copper, zinc, and gold, or alloys 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:Al or SNO _{2 :Sb;} Poly(3-methylthiophene), poly[3,4-(ethylene-1,2-dioxy)thiophene] (PEDOT), conductive polymers such as polypyrrole and polyaniline, and the like, but are not limited thereto.

It is preferable that the cathode material is a material having a small work function to facilitate electron injection into the organic material layer. Specific examples of the negative electrode material include metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin and lead, or alloys thereof; There are multilayered materials such as LiF/Al or LiO ₂ /Al, but are not limited thereto.

The hole injection layer is a layer that injects holes from the electrode, and has the ability to transport holes as a hole injection material, so that it has a hole injection effect at the anode, an excellent hole injection effect for the light emitting layer or the light emitting material, and is generated from the light emitting layer. A compound that prevents the movement of excitons to the electron injection layer or the electron injection material and has excellent ability to form a thin film is preferable. It is preferable that the HOMO (highest occupied molecular orbital) of the hole injection material is between the work function of the positive electrode material and the HOMO of the surrounding organic material layer. Specific examples of hole injection materials include metal porphyrin, oligothiophene, arylamine-based organic substances, hexanitrile hexaazatriphenylene-based organic substances, quinacridone-based organic substances, and perylene-based organic substances. Organic substances, anthraquinone, polyaniline, and polythiophene-based conductive polymers, but are not limited thereto.

The hole transport layer is a layer that receives holes from the hole injection layer and transports holes to the light emitting layer.As a hole transport material, a material capable of transporting holes from the anode or the hole injection layer to the light emitting layer and having high mobility for holes This is suitable. Specific examples include an arylamine-based organic material, a conductive polymer, and a block copolymer including a conjugated portion and a non-conjugated portion, but are not limited thereto.

The electron blocking layer is formed on the hole transport layer and is preferably provided in contact with the light emitting layer to control hole mobility and prevent excessive movement of electrons to increase the probability of hole-electron coupling, thereby increasing the efficiency of the organic light-emitting device. It serves to improve. The electron blocking layer includes an electron blocking material, and a material having a stable structure in which electrons do not flow out of the emission layer is suitable as the electron blocking material. As a specific example, an arylamine-based organic material may be used, but is not limited thereto.

As the light-emitting material, a material capable of emitting light in a visible light region by transporting and combining holes and electrons from the hole transport layer and the electron transport layer, respectively, and a material having good quantum efficiency for fluorescence or phosphorescence is preferable. Specific examples of 8-hydroxy-quinoline aluminum complex (Alq ₃ ); Carbazole-based compounds; Dimerized styryl compounds; BAlq; 10-hydroxybenzoquinoline-metal compound; Benzoxazole, benzthiazole, and benzimidazole-based compounds; Poly(p-phenylenevinylene) (PPV)-based polymer; Spiro compounds; Polyfluorene, rubrene, and the like, but are not limited thereto.

The emission layer may include a host material and a dopant material. Host materials include condensed aromatic ring derivatives or heterocyclic-containing compounds. Specifically, condensed aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, and fluoranthene compounds, and heterocycle-containing compounds include carbazole derivatives, dibenzofuran derivatives, ladder type Furan compounds, pyrimidine derivatives, and the like, but are not limited thereto.

Dopant materials include aromatic amine derivatives, strylamine compounds, boron complexes, fluoranthene compounds, and metal complexes. Specifically, the aromatic amine derivative is a condensed aromatic ring derivative having a substituted or unsubstituted arylamino group, and includes pyrene, anthracene, chrysene, periflanthene and the like having an arylamino group, and the styrylamine compound is substituted or unsubstituted As a compound in which at least one arylvinyl group is substituted on the arylamine, one or two or more substituents selected from the group consisting of aryl group, silyl group, alkyl group, cycloalkyl group, and arylamino group are substituted or unsubstituted. Specifically, there are styrylamine, styryldiamine, styryltriamine, and styryltetraamine, but are not limited thereto. In addition, examples of the metal complex include, but are not limited to, an iridium complex and a platinum complex.

The electron transport layer is a layer that receives electrons from the electron injection layer and transports electrons to the emission layer. As an electron transport material, a material capable of injecting electrons from the cathode and transferring them to the emission layer, and a material having high mobility for electrons is suitable. Do. Specific examples include Al complex of 8-hydroxyquinoline; Complexes containing Alq _3; Organic radical compounds; Hydroxyflavone-metal complexes and the like, but are not limited thereto. The electron transport layer can be used with any desired cathode material as used according to the prior art. In particular, examples of suitable cathode materials are conventional materials that have a low work function and are followed by an aluminum layer or a silver layer. Specifically, they are cesium, barium, calcium, ytterbium, and samarium, and in each case an aluminum layer or a silver layer follows.

The electron injection layer is a layer that injects electrons from the electrode, has the ability to transport electrons, has an electron injection effect from the cathode, an excellent electron injection effect for the light emitting layer or the light emitting material, and hole injection of excitons generated in the light emitting layer A compound that prevents migration to the layer and is excellent in thin film forming ability is preferable. Specifically, fluorenone, anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylene tetracarboxylic acid, preorenylidene methane, anthrone, etc. Complex compounds and nitrogen-containing 5-membered ring derivatives, but are not limited thereto.

Examples of the metal complex compound include 8-hydroxyquinolinato lithium, bis(8-hydroxyquinolinato)zinc, bis(8-hydroxyquinolinato)copper, bis(8-hydroxyquinolinato)manganese, Tris(8-hydroxyquinolinato)aluminum, tris(2-methyl-8-hydroxyquinolinato)aluminum, tris(8-hydroxyquinolinato)gallium, bis(10-hydroxybenzo[h] Quinolinato)beryllium, bis(10-hydroxybenzo[h]quinolinato)zinc, bis(2-methyl-8-quinolinato)chlorogallium, bis(2-methyl-8-quinolinato)( o-cresolato)gallium, bis(2-methyl-8-quinolinato)(1-naphtholato)aluminum, bis(2-methyl-8-quinolinato)(2-naphtholato)gallium, etc. It is not limited to this.

The organic light-emitting device according to the present invention may be a top emission type, a bottom emission type, or a double-sided emission type depending on the material used.

In addition, the compound represented by Formula 1 may be included in an organic solar cell or an organic transistor in addition to the organic light emitting device.

The preparation of the compound represented by Formula 1 and the organic light-emitting device including the same will be described in detail in the following Examples. However, the following examples are for illustrating the present invention, and the scope of the present invention is not limited thereto.

[Production Example]

Preparation Example 1: Preparation of compounds A-1 to A-2

1) Preparation of compound A-1

2-chloro-9H-carbazole (30.0 g, 138.1 mmol) and 2-bromodibenzo[b,e][1,4]dioxine (36.2 g, 138.1 mmol) were dissolved in 300 mL of xylene, and sodium tertiary-butoxide Add side (19.9g, 207.1 mmol) and warm. Bis (tri tertiary-butylphosphine) palladium (2.2g, 3mol%) was added and stirred under reflux for 12 hours. When the reaction was completed, the temperature was lowered to room temperature and the resulting solid was filtered. The solid was dissolved in 700 mL of chloroform, washed twice with water, and the organic layer was separated, anhydrous magnesium sulfate was added thereto, stirred, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified through a silica column using chloroform and ethyl acetate to prepare a white solid compound A-1 (37.0 g, 70%).

MS: [M+H]+ = 384

2) Preparation of compound A-2

Compound A-1 (37.0 g, 96.7 mmol), bis (pinacolato) diboron (27.0 g, 106.3 mmol) and potassium acetate (19.0 g, 193.3 mmol) were mixed in a nitrogen atmosphere, and added to 300 ml of dioxane. Heated while stirring. In a refluxed state, bis(dibenzylidineacetone)palladium (1.7 g, 3 mol%) and tricyclohexylphosphine (1.6 g, 6 mol%) were added, followed by heating and stirring for 5 hours. After the reaction was completed, the temperature was lowered to room temperature and then filtered. Water was poured into the filtrate, extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. After distillation under reduced pressure and recrystallized with ethanol, compound A-2 (36.7g, 80%) was prepared.

MS: [M+H]+ = 476

Preparation Example 2: Preparation of Compounds B-1 to B-2

1) Preparation of compound B-1

3-chloro-9H-carbazole (30.0 g, 138.1 mmol) and 2-bromodibenzo[b,e][1,4]dioxine (36.2 g, 138.1 mmol) were dissolved in 300 mL of xylene, and sodium tertiary-butoxide Add side (19.9g, 207.1 mmol) and warm. Bis (tri tertiary-butylphosphine) palladium (2.2g, 3mol%) was added and stirred under reflux for 12 hours. When the reaction was completed, the temperature was lowered to room temperature and the resulting solid was filtered. The solid was dissolved in 700 mL of chloroform, washed twice with water, and the organic layer was separated, anhydrous magnesium sulfate was added thereto, stirred, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified through a silica column using chloroform and ethyl acetate to prepare a white solid compound B-1 (39.1 g, 74%).

MS: [M+H]+ = 384

2) Preparation of compound B-2

Compound B-1 (39.1 g, 102.2 mmol), bis (pinacolato) diboron (28.5 g, 112.4 mmol) and potassium acetate (20.1 g, 204.4 mmol) were mixed in a nitrogen atmosphere, and added to 300 ml of dioxane. Heated while stirring. In a refluxed state, bis(dibenzylidineacetone)palladium (1.8 g, 3 mol%) and tricyclohexylphosphine (1.7 g, 6 mol%) were added, followed by heating and stirring for 5 hours. After the reaction was completed, the temperature was lowered to room temperature and then filtered. Water was poured into the filtrate, extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. After distillation under reduced pressure and recrystallized with ethanol, compound B-2 (37.4g, 77%) was prepared.

MS: [M+H]+ = 476

Preparation Example 3: Preparation of compounds C-1 to C-2

1) Preparation of compound C-1

4-chloro-9H-carbazole (30.0 g, 138.1 mmol) and 2-bromodibenzo[b,e][1,4]dioxine (36.2 g, 138.1 mmol) were dissolved in 300 mL of xylene, and sodium tertiary-butoxide Add side (19.9g, 207.1 mmol) and warm. Bis (tri tertiary-butylphosphine) palladium (2.2g, 3mol%) was added and stirred under reflux for 12 hours. When the reaction was completed, the temperature was lowered to room temperature and the resulting solid was filtered. The solid was dissolved in 700 mL of chloroform, washed twice with water, and the organic layer was separated, anhydrous magnesium sulfate was added thereto, stirred, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified through a silica column using chloroform and ethyl acetate to prepare a white solid compound C-1 (31.2 g, 59%).

MS: [M+H]+ = 384

2) Preparation of compound C-2

Compound C-1 (31.2 g, 102.2 mmol), bis (pinacolato) diboron (22.8 g, 89.6 mmol) and potassium acetate (16.0 g, 162.9 mmol) were mixed in a nitrogen atmosphere, and added to 300 ml of dioxane. Heated while stirring. In a refluxed state, bis(dibenzylidineacetone)palladium (1.4 g, 3 mol%) and tricyclohexylphosphine (1.4 g, 6 mol%) were added, followed by heating and stirring for 5 hours. After the reaction was completed, the temperature was lowered to room temperature and then filtered. Water was poured into the filtrate, extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. After distillation under reduced pressure and recrystallized with ethanol, compound C-2 (34.4g, 81%) was prepared.

MS: [M+H]+ = 476

Preparation Example 4: Preparation of Compounds D-1 to D-2

1) Preparation of compound D-1

2-chloro-9H-carbazole (30.0 g, 138.1 mmol) and 1-bromodibenzo[b,e][1,4]dioxine (36.2 g, 138.1 mmol) were dissolved in 300 mL of xylene, and sodium tertiary-butoxide Add side (19.9g, 207.1 mmol) and warm. Bis (tri tertiary-butylphosphine) palladium (2.2g, 3mol%) was added and stirred under reflux for 12 hours. When the reaction was completed, the temperature was lowered to room temperature and the resulting solid was filtered. The solid was dissolved in 700 mL of chloroform, washed twice with water, and the organic layer was separated, anhydrous magnesium sulfate was added thereto, stirred, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified through a silica column using chloroform and ethyl acetate to prepare a white solid compound D-1 (34.9 g, 66%).

MS: [M+H]+ = 384

2) Preparation of compound D-2

Compound D-1 (34.9 g, 91.1 mmol), bis (pinacolato) diboron (25.5 g, 100.2 mmol) and potassium acetate (17.9 g, 182.3 mmol) were mixed in a nitrogen atmosphere, and added to 300 ml of dioxane. Heated while stirring. In a refluxed state, bis(dibenzylidineacetone)palladium (1.6 g, 3 mol%) and tricyclohexylphosphine (1.5 g, 6 mol%) were added, followed by heating and stirring for 5 hours. After the reaction was completed, the temperature was lowered to room temperature and then filtered. Water was poured into the filtrate, extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. After distillation under reduced pressure and recrystallized with ethanol, compound D-2 (33.3g, 77%) was prepared.

MS: [M+H]+ = 476

Preparation Example 5: Preparation of compounds E-1 to E-2

1) Preparation of compound E-1

3-chloro-9H-carbazole (30.0 g, 138.1 mmol) and 1-bromodibenzo[b,e][1,4]dioxine (36.2 g, 138.1 mmol) were dissolved in 300 mL of xylene, and sodium tertiary-butoxide Add side (19.9g, 207.1 mmol) and warm. Bis (tri tertiary-butylphosphine) palladium (2.2g, 3mol%) was added and stirred under reflux for 12 hours. When the reaction was completed, the temperature was lowered to room temperature and the resulting solid was filtered. The solid was dissolved in 700 mL of chloroform, washed twice with water, and the organic layer was separated, anhydrous magnesium sulfate was added thereto, stirred, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified through a silica column using chloroform and ethyl acetate to prepare a white solid compound E-1 (30.0 g, 51%).

MS: [M+H]+ = 384

2) Preparation of compound E-2

Compound E-1 (27.0 g, 70.4 mmol), bis (pinacolato) diboron (19.7 g, 77.5 mmol) and potassium acetate (13.8 g, 140.8 mmol) were mixed in a nitrogen atmosphere, and added to 300 ml of dioxane. Heated while stirring. In a refluxed state, bis(dibenzylidineacetone)palladium (1.2 g, 3 mol%) and tricyclohexylphosphine (1.2 g, 6 mol%) were added, followed by heating and stirring for 5 hours. After the reaction was completed, the temperature was lowered to room temperature and then filtered. Water was poured into the filtrate, extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. After distillation under reduced pressure and recrystallized with ethanol, compound E-2 (27.1g, 81%) was prepared.

MS: [M+H]+ = 476

Preparation Example 6: Preparation of Compounds F-1 to F-2

1) Preparation of compound F-1

4-chloro-9H-carbazole (30.0 g, 138.1 mmol) and 1-bromodibenzo[b,e][1,4]dioxine (36.2 g, 138.1 mmol) were dissolved in 300 mL of xylene, and sodium tertiary-butoxide Add side (19.9g, 207.1 mmol) and warm. Bis (tri tertiary-butylphosphine) palladium (2.2g, 3mol%) was added and stirred under reflux for 12 hours. When the reaction was completed, the temperature was lowered to room temperature and the resulting solid was filtered. The solid was dissolved in 700 mL of chloroform, washed twice with water, and the organic layer was separated, anhydrous magnesium sulfate was added thereto, stirred, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified through a silica column using chloroform and ethyl acetate to prepare a white solid compound F-1 (33.3 g, 63%).

MS: [M+H]+ = 384

2) Preparation of compound F-2

Compound F-1 (33.3 g, 87.0 mmol), bis (pinacolato) diboron (24.3 g, 95.7 mmol) and potassium acetate (17.1 g, 174.0 mmol) were mixed in a nitrogen atmosphere, and added to 300 ml of dioxane. Heated while stirring. In a refluxed state, bis(dibenzylidineacetone)palladium (1.5 g, 3 mol%) and tricyclohexylphosphine (1.5 g, 6 mol%) were added, followed by heating and stirring for 5 hours. After the reaction was completed, the temperature was lowered to room temperature and then filtered. Water was poured into the filtrate, extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. After distillation under reduced pressure and recrystallized with ethanol, compound F-2 (34.7g, 84%) was prepared.

MS: [M+H]+ = 476

Preparation Example 7: Preparation of Compound 1

In a nitrogen atmosphere, compound A-2 (20.0 g, 43.7 mmol) and 2-chloro-4,6-diphenyl-1,3,5-triazine (11.7 g, 43.7 mmol) were added to 200 ml of tetrahydrofuran and stirred and refluxed. I did. Thereafter, potassium carbonate (12.1 g, 87.5 mmol) was dissolved in 30 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.5 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 1 (13.7 g, 54%) was prepared through recrystallization of ethyl acetate.

MS: [M+H]+ = 581

Preparation Example 8: Preparation of Compound 2

In a nitrogen atmosphere, compound B-2 (20.0 g, 43.7 mmol) and 2-chloro-4,6-diphenyl-1,3,5-triazine (11.7 g, 43.7 mmol) were added to 200 ml of tetrahydrofuran and stirred and refluxed. I did. Thereafter, potassium carbonate (12.1 g, 87.5 mmol) was dissolved in 30 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.5 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 2 (13.2 g, 52%) was prepared through recrystallization of ethyl acetate.

MS: [M+H]+ = 581

Preparation Example 9: Preparation of compound 3

In a nitrogen atmosphere, compound C-2 (20.0 g, 43.7 mmol) and 2-chloro-4,6-diphenyl-1,3,5-triazine (11.7 g, 43.7 mmol) were added to 200 ml of tetrahydrofuran and stirred and refluxed. I did. Thereafter, potassium carbonate (12.1 g, 87.5 mmol) was dissolved in 30 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.5 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 3 (15.5 g, 61%) was prepared through ethyl acetate recrystallization.

MS: [M+H]+ = 581

Preparation Example 10: Preparation of compound 4

In a nitrogen atmosphere, compound D-2 (20.0 g, 43.7 mmol) and 2-chloro-4,6-diphenyl-1,3,5-triazine (11.7 g, 43.7 mmol) were added to 200 ml of tetrahydrofuran and stirred and refluxed. I did. Thereafter, potassium carbonate (12.1 g, 87.5 mmol) was dissolved in 30 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.5 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 4 (12.4 g, 49%) was prepared through recrystallization of ethyl acetate.

MS: [M+H]+ = 581

Preparation Example 11: Preparation of compound 5

In a nitrogen atmosphere, compound E-2 (20.0 g, 43.7 mmol) and 2-chloro-4,6-diphenyl-1,3,5-triazine (11.7 g, 43.7 mmol) were added to 200 ml of tetrahydrofuran and stirred and refluxed. I did. Thereafter, potassium carbonate (12.1 g, 87.5 mmol) was dissolved in 30 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.5 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 5 (11.2 g, 44%) was prepared through recrystallization of ethyl acetate.

MS: [M+H]+ = 581

Preparation Example 12: Preparation of compound 6

In a nitrogen atmosphere, compound F-2 (20.0 g, 43.7 mmol) and 2-chloro-4,6-diphenyl-1,3,5-triazine (11.7 g, 43.7 mmol) were added to 200 ml of tetrahydrofuran and stirred and refluxed. I did. Thereafter, potassium carbonate (12.1 g, 87.5 mmol) was dissolved in 30 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.5 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 6 (16.2 g, 64%) was prepared through recrystallization of ethyl acetate.

MS: [M+H]+ = 581

Preparation Example 13: Preparation of compound 7

1) Preparation of compound 7-1

In a nitrogen atmosphere, compound A-2 (20.0 g, 43.7 mmol) and 2-bromo-7-chlorodibenzo[b,d]furan (12.2 g, 43.7 mmol) were added to 200 ml of tetrahydrofuran, followed by stirring and refluxing. Thereafter, potassium carbonate (12.1 g, 87.5 mmol) was dissolved in 30 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.5 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 7-1 (18.7 g, 78%) was prepared through ethyl acetate recrystallization.

MS: [M+H]+ = 550

2) Preparation of compound 7-2

Compound 7-1 (18.7 g, 34.1 mmol), bis (pinacolato) diboron (9.5 g, 37.5 mmol) and potassium acetate (6.7 g, 68.1 mmol) were mixed in a nitrogen atmosphere, and added to 200 ml of dioxane. Heated while stirring. In a refluxed state, bis(dibenzylidineacetone)palladium (0.6 g, 3 mol%) and tricyclohexylphosphine (0.6 g, 6 mol%) were added, followed by heating and stirring for 5 hours. After the reaction was completed, the temperature was lowered to room temperature and then filtered. Water was poured into the filtrate, extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. After distillation under reduced pressure and recrystallized with ethanol, compound 7-2 (18.3g, 84%) was prepared.

MS: [M+H]+ = 642

3) Preparation of compound 7

In a nitrogen atmosphere, compound 7-2 (18.3 g, 28.5 mmol) and 2-chloro-4,6-diphenyl-1,3,5-triazine (7.6 g, 28.5 mmol) were added to 100 ml of tetrahydrofuran and stirred and refluxed. I did. Thereafter, potassium carbonate (7.9 g, 57.1 mmol) was dissolved in 20 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.0 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 7 (11.7 g, 55%) was prepared through recrystallization of ethyl acetate.

MS: [M+H]+ = 747

Preparation 14: Preparation of compound 8

Compound A-2 (20.0 g, 43.7 mmol) and 2-([1,1'-biphenyl]-4-yl)-4-chloro-6-phenyl-1,3,5-triazine (15.0 g) in a nitrogen atmosphere , 43.7 mmol) was added to 200 ml of tetrahydrofuran and stirred and refluxed. Thereafter, potassium carbonate (12.1 g, 87.5 mmol) was dissolved in 30 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.5 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 8 (19.8 g, 69%) was prepared through recrystallization of ethyl acetate.

MS: [M+H]+ = 657

Preparation Example 15: Preparation of compound 9

Compound A-2 (20.0 g, 43.7 mmol) and 2-([1,1'-biphenyl]-3-yl)-4-chloro-6-phenyl-1,3,5-triazine (15.0 g) in a nitrogen atmosphere , 43.7 mmol) was added to 200 ml of tetrahydrofuran and stirred and refluxed. Thereafter, potassium carbonate (12.1 g, 87.5 mmol) was dissolved in 30 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.5 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 9 (12.3 g, 43%) was prepared through recrystallization of ethyl acetate.

MS: [M+H]+ = 657

Preparation Example 16: Preparation of compound 10

Compound A-2 (20.0 g, 43.7 mmol) and 2-chloro-4-(dibenzo[b,d]furan-4-yl)-6-phenyl-1,3,5-triazine (15.0 g, 43.7 mmol) was added to 200 ml of tetrahydrofuran and stirred and refluxed. Thereafter, potassium carbonate (12.1 g, 87.5 mmol) was dissolved in 30 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.5 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 10 (16.1 g, 55%) was prepared through ethyl acetate recrystallization.

MS: [M+H]+ = 671

Preparation Example 17: Preparation of compound 11

Compound A-2 (20.0 g, 43.7 mmol) and 9-(4-chloro-6-phenyl-1,3,5-triazin-2-yl)-9H-carbazole (15.6 g, 43.7 mmol) were mixed in a nitrogen atmosphere. Into 200 ml of tetrahydrofuran, it was stirred and refluxed. Thereafter, potassium carbonate (12.1 g, 87.5 mmol) was dissolved in 30 ml of water, and after sufficiently stirring, tetrakistriphenyl-phosphinopalladium (1.5 g, 3 mol%) was added. After the reaction for 4 hours, the temperature was lowered to room temperature and filtered. The filtrate was dissolved in chloroform, extracted with water, and the organic layer was dried over magnesium sulfate. After drying the organic layer, compound 11 (11.4 g, 39%) was prepared through recrystallization of ethyl acetate.

MS: [M+H]+ = 670

[Experimental Example]

<Experimental Example 1>

A glass substrate coated with a thin film of ITO (indium tin oxide) to a thickness of 1,300Å was put in distilled water dissolved in a detergent and washed with ultrasonic waves. At this time, a product made by Fischer Co. was used as a detergent, and distilled water secondarily filtered with a filter manufactured by Millipore Co. was used as distilled water. After washing the ITO for 30 minutes, it was repeated twice with distilled water to perform ultrasonic cleaning for 10 minutes. After washing with distilled water, ultrasonic washing was performed with a solvent of isopropyl alcohol, acetone, and methanol, dried, and then transported to a plasma cleaner. In addition, after cleaning the substrate for 5 minutes using oxygen plasma, the substrate was transported to a vacuum evaporator.

On the ITO transparent electrode prepared as described above, the following HI-1 compound was thermally vacuum deposited to a thickness of 50 Å to form a hole injection layer. On the hole injection layer, the following HT-1 compound was thermally vacuum deposited to a thickness of 250 Å to form a hole transport layer, and the following HT-2 compound was vacuum deposited on the HT-1 evaporated film to a thickness of 50 Å to form an electron blocking layer. A light emitting layer having a thickness of 400 Å was formed by co-depositing Compound 1 prepared in Preparation Example, the following YGH-1 compound, and phosphorescent dopant YGD-1 as a light emitting layer on the HT-2 deposited film at a weight ratio of 44:44:12. On the light emitting layer, the following ET-1 compound was vacuum-deposited to a thickness of 250 Å to form an electron transport layer, and the following ET-2 compound and Li were vacuum deposited on the electron transport layer at a weight ratio of 98:2 to form an electron injection layer having a thickness of 100 Å. Formed. A cathode was formed by depositing aluminum to a thickness of 1000 Å on the electron injection layer.

In the above process, the deposition rate of the organic material was maintained at 0.4 ~ 0.7 Å/sec, the deposition rate of aluminum was maintained at 2 Å/sec, and the vacuum degree during deposition was maintained at 1 × 10 ^-7 ~ 5 × 10 ^-8 torr. I did.

<Experimental Examples 2 to 11>

In Experimental Example 1, an organic light-emitting device was manufactured in the same manner as in Experimental Example 1, except that the compound shown in Table 1 was used instead of Compound 1 of Preparation Example.

<Comparative Experimental Examples 1 to 2>

In Experimental Example 1, an organic light-emitting device was manufactured in the same manner as in Experimental Example 1, except that the compound shown in Table 1 was used instead of Compound 1 of Preparation Example. The compounds of CE1 to CE2 in Table 1 are as follows.

In the above Experimental Examples and Comparative Experimental Examples, voltage and efficiency of the organic light-emitting device were measured at a current density of ^{10 mA/cm 2 , and life was measured at a current density of 50 mA/cm 2} , and the results are shown in Table 1 below. In this case, LT ₉₅ refers to a time when it becomes 95% of the initial luminance.

compound Voltage(V)
(@10mA/cm ² ) Efficiency (Cd/A)
(@10mA/cm ² ) Color coordinates
(x,y) Life(h)
(LT ₉₅ at 50mA/cm ² ) Experimental Example 1 Compound 1 4.2 78 0.45, 0.53 145 Experimental Example 2 Compound 2 4.1 77 0.46, 0.53 130 Experimental Example 3 Compound 3 4.1 78 0.46, 0.54 154 Experimental Example 4 Compound 4 4.0 78 0.46, 0.54 140 Experimental Example 5 Compound 5 4.2 77 0.46, 0.53 125 Experimental Example 6 Compound 6 4.2 76 0.46, 0.54 135 Experimental Example 7 Compound 7 4.1 75 0.46, 0.54 127 Experimental Example 8 Compound 8 4.1 80 0.46, 0.54 114 Experimental Example 9 Compound 9 4.3 79 0.46, 0.53 155 Experimental Example 10 Compound 10 4.4 77 0.46, 0.54 110 Experimental Example 11 Compound 11 4.4 76 0.46, 0.54 130 Comparative Experimental Example 1 CE1 4.5 70 0.46, 0.54 90 Comparative Experiment 2 CE2 4.5 67 0.46, 0.55 45

As shown in Table 1, when the compound of the present invention was used as a light emitting layer material, it was confirmed that the compound of the present invention exhibited excellent characteristics in terms of efficiency and lifetime compared to the comparative experimental example. This is believed to be due to an increase in the electronic stability of the compound represented by Formula 1 as the dioxin group is additionally substituted with the carbazole group.

1: substrate 2: anode
3: light-emitting layer 4: cathode
5: hole injection layer 6: hole transport layer
7: electron blocking layer 8: electron transport layer
9: electron injection layer

Claims (8)

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

In Formula 1,
a to d are each independently an integer of 0 to 3,
L is a single bond; Substituted or unsubstituted C _6-60 arylene; Dibenzofurandiyl; Dibenzothiophendiyl; Carbazoldiyl; Phenylene-carbazoldiyl; Or phenylene-naphthalenediyl,
X is each independently N or C (R ₅ ), provided that at least one of X is N,
Ar ₁ and Ar ₂ are each independently hydrogen; Substituted or unsubstituted C _6-60 aryl;

;

;

;

;

; or

ego,
R ₁ to R ₅ are each independently hydrogen or deuterium.
The method of claim 1,
Formula 1 is a compound represented by the following Formula 1-1 or 1-2:
[Formula 1-1]

[Formula 1-2]

In Formula 1-1 or 1-2,
Descriptions of a to d, R ₁ to R ₄ , L, X, Ar ₁ and Ar ₂ are as defined in claim 1.
The method of claim 1,
a, b, c and d are 0, the compound.
The method of claim 1,
L is a single bond; Phenylene; Biphenyldiyl; Naphthalenediyl; Dimethylfluorenediyl; Dibenzofurandiyl; Dibenzothiophendiyl; Carbazoldiyl; Phenylene-carbazoldiyl; Or phenylene-naphthalenediyl.
The method of claim 1,
X is all N, the compound.
The method of claim 1,
Ar ₁ and Ar ₂ are each independently any one selected from the group consisting of:

.
The method of claim 1,
The compound represented by Formula 1 is any one selected from the group consisting of:

A first electrode; A second electrode provided to face the first electrode; And one or more organic material layers provided between the first electrode and the second electrode, wherein at least one of the organic material layers contains the compound according to any one of claims 1 to 7 That is, an organic light emitting device.

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