KR102020029B1 - Novel hetero-cyclic 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

New heterocyclic compound and organic light emitting device using the same {NOVEL HETERO-CYCLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME}

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

In general, organic light emitting phenomenon refers to a phenomenon of converting electrical energy into light energy using an organic material. The organic light emitting device using the organic light emitting phenomenon has a wide viewing angle, excellent contrast, fast response time, excellent brightness, driving voltage and response speed characteristics, many studies have been conducted.

The 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 to increase the efficiency and stability of the organic light emitting device, for example, it may be made of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer. When the voltage is applied between the two electrodes in the structure of the organic light emitting device, holes are injected into the organic material layer at the anode and electrons are injected into the organic material layer, and excitons are formed when the injected holes and the electrons meet each other. When it falls back to the ground, it glows.

There is a continuous demand for the development of new materials for organic materials used in such organic light emitting devices.

Korean Patent Publication No. 10-2000-0051826

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

The present invention provides a compound represented by Formula 1:

[Formula 1]

In Chemical Formula 1,

X is O or S,

Two adjacent ones of R ₁ to R ₃ are respectively bonded to * of Formula 2 to form a fused ring, and the other is hydrogen;

One of R ₄ and R ₅ is bonded with * in Formula 3, and the other is hydrogen;

[Formula 2]

[Formula 3]

In Chemical Formula 3,

L is a bond; Substituted or unsubstituted C _6-60 arylene; Or C _2-60 heteroarylene containing one or more heteroatoms selected from the group consisting of substituted or unsubstituted O, N, Si, and S,

Z are each independently N, or CH, provided that at least one of Z is N,

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

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 one or more layers of the organic material layers include the compound represented by Chemical Formula 1. .

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

FIG. 1 shows an example of an organic light emitting element composed of a substrate 1, an anode 2, a light emitting layer 3, and a cathode 4. As shown in FIG.
FIG. 2 shows an example of an organic light emitting element consisting of a substrate 1, an anode 2, a hole injection layer 5, a hole transport layer 6, a light emitting layer 7, an electron transport layer 8 and a cathode 4 It is.

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

, 또는

는 다른 치환기에 연결되는 결합을 의미하고, 단일 결합은 L 로 표시되는 부분에 별도의 원자가 존재하지 않은 경우를 의미한다. In this specification,

, or

Means a bond connected to another substituent, and a single bond means a case where no separate atom is present in a portion represented by L.

As used herein, the term "substituted or unsubstituted" is deuterium; Halogen group; Cyano group; Nitro group; Hydroxyl group; Carbonyl group; Ester group; Imide group; Amino group; Phosphine oxide groups; An alkoxy group; Aryloxy group; Alkyl thioxy group; Arylthioxy group; Alkyl sulfoxy groups; Aryl sulfoxy group; Silyl groups; Boron group; An alkyl group; Cycloalkyl group; Alkenyl groups; Aryl group; Aralkyl group; Ar alkenyl group; Alkylaryl group; Alkylamine group; Aralkyl amine groups; Heteroarylamine group; Arylamine group; Aryl phosphine group; Or substituted or unsubstituted with one or more substituents selected from the group consisting of heterocyclic groups including one or more of N, O and S atoms, or two or more substituents of the above-described substituents connected or substituted. . For example, "a substituent to which two or more substituents are linked" 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 linked.

Although carbon number of a carbonyl group in this specification is not specifically limited, It is preferable that it is C1-C40. Specifically, it may be a compound having a structure as follows, but is not limited thereto.

In the present specification, the oxygen of the ester group may be substituted with a linear, branched or cyclic alkyl group having 1 to 25 carbon atoms or an aryl group having 6 to 25 carbon atoms. Specifically, it may be a compound of the following structural formula, but is not limited thereto.

In this specification, although carbon number of an imide group is not specifically limited, It is preferable that it is C1-C25. Specifically, it may be a compound having a structure as follows, but is not limited thereto.

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

In the present specification, the boron group specifically includes, but is not limited to, trimethylboron group, triethylboron group, t-butyldimethylboron group, triphenylboron group, phenylboron group, and the like.

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 chain, carbon number 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, cyclohexylmethyl, 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 is not limited thereto.

In the present specification, the alkenyl group may be linear or branched chain, the carbon number 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 one 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 preferably has 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 monocyclic aryl group, but may be a phenyl group, a biphenyl group, a terphenyl group, etc., but is not limited thereto. The polycyclic aryl group may be naphthyl group, anthracenyl group, phenanthryl group, pyrenyl group, perylenyl group, chrysenyl group, 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,

And so on. However, the present invention is not limited thereto.

In the present specification, the heterocyclic group is a heterocyclic group containing one or more of O, N, Si, and S as a dissimilar element, and the carbon number 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, triazole 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 (phenanthroline), thiazolyl group, Isooxazolyl group, oxdiazolyl group, thiadiazolyl group, benzothiazolyl group, phenothiazinyl group, dibenzofuranyl group and the like, but is not limited thereto.

In the present specification, the aryl group in 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 alkyl group described above. In the present specification, the heteroaryl of the heteroarylamine may be applied to the description of the aforementioned heterocyclic group. In the present specification, the alkenyl group in 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 aforementioned aryl group or cycloalkyl group may be applied except that two substituents are formed by bonding. In the present specification, the heterocyclic group is not a monovalent group, and the description of the aforementioned heterocyclic group may be applied except that two substituents are formed by bonding.

On the other hand, the present invention provides a compound represented by the formula (1).

In Formula 1, X is O or S.

In Formula 1, two adjacent ones of R ₁ to R ₃ each combine with * in Formula 2 to form a fused ring, and the rest are hydrogen. Two adjacent functional groups of R ₁ to R ₃ of Formula 1 mean a functional group group each substituted on two carbon atoms chemically bonded to each other in Formula 1, for example, (R ₁ and R ₂ ), (R ₂ and R ₃ ) may correspond.

Specifically, for example, in Formula 1, R ₁ and R ₂ may combine with * of Formula 2 to form a fused ring, or in Formula 1, R ₂ and R ₃ may combine with * of Formula 2 to form a fused ring Can be formed.

In Formula 1, after two adjacent ones of R ₁ to R ₃ each combine with * of Formula 2 to form a fused ring, the remaining functional group that does not form a bond with * of Formula 2 may be hydrogen.

That is, the compound may be represented by the following Chemical Formula 1-1 or 1-2:

[Formula 1-1]

[Formula 1-2]

In Chemical Formulas 1-1 and 1-2,

X, R ₄ and R ₅ are the same as defined in Formula 1 above.

Meanwhile, two adjacent ones of R ₁ to R ₃ of Formula 1 may combine with each of * of Formula 2 to form a fused ring, and at the same time, one of R ₄ and R ₅ of Formula 1 may represent Can be combined.

In this case, after one of R ₄ and R ₅ combines with * of Formula 3 to form a fused ring, the remaining functional group that does not form a bond with * of Formula 3 may be hydrogen.

As such, two adjacent groups of R ₁ to R ₃ of Formula 1 may combine with each of * of Formula 2 to form a fused ring, and at the same time, one of R ₄ and R ₅ of Formula 1 may be represented by * of Formula 3 As combined, the organic light emitting device using the compound of Formula 1 may have high efficiency, low driving voltage, high brightness and long life.

On the other hand, in Formula 3,

L may be a bond, substituted or unsubstituted phenylene, substituted or unsubstituted biphenylene, or substituted or unsubstituted naphthylene, and more specifically, L ₁ may be a bond or phenylene. Examples of the phenylene may be any one selected from the group consisting of:

.

.

In Formula 3, Z is each independently N, or CH, provided that at least one of Z may be N.

In addition, in Formula 3, Ar ₁ and Ar ₂ are each independently, substituted or unsubstituted C _6-60 aryl; Or C 2 _-60 heteroaryl containing one or more heteroatoms selected from the group consisting of substituted or unsubstituted O, N, Si and S. For more specific examples, Ar ₁ and Ar ₂ may each independently be phenyl, biphenylyl, terphenylyl, dimethylfluorenyl, naphthyl, pyridinyl, dibenzofuranyl, or dibenzothiophenyl. have.

In addition, the compound may be any one selected from the group consisting of the following compounds:

On the other hand, the present invention provides an organic light emitting device comprising the compound represented by the formula (1). In one embodiment, 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 one or more layers of the organic material layers include the compound represented by Chemical Formula 1. .

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, 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.

The organic material layer may include a hole injection layer, a hole transport layer, or a layer for simultaneously injecting and transporting holes, and the hole injection layer, a hole transport layer, or a layer for simultaneously injecting holes and transporting holes may be represented by Chemical Formula 1 above. It may include a compound represented.

In addition, the organic material layer may include a light emitting layer, and the light emitting layer may include a compound represented by Chemical Formula 1.

In addition, the electron transport layer, the electron injection layer, or may include a layer for simultaneously transporting electrons and electron injection, the electron transport layer, the electron injection layer, or a layer for the simultaneous transport and electron injection is represented by the formula (1) It may include a compound.

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

In addition to the organic layer, the organic light emitting device may include an electron blocking layer (EBL) positioned between the hole transport layer and the light emitting layer and / or a hole blocking layer disposed between the light emitting layer and the electron transport layer. layer: HBL) may be further included. In such a structure, the compound represented by Formula 1 may be included in one or more layers of the electron blocking layer and the hole blocking layer. The electron blocking layer and the hole blocking layer may each be an organic material layer adjacent to the emission layer.

In this case, the compound represented by Chemical Formula 1 may be included in the emission layer, the electron transport layer, or the hole blocking layer.

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 further includes a hole injection layer and a hole transport layer between the first electrode and the light emitting layer, an electron transport layer and an electron injection layer between the light emitting layer and the second electrode, in addition to the light emitting layer as an organic layer. It may have a structure to. However, the structure of the organic light emitting device is not limited thereto, and may include fewer or more organic layers.

In addition, the organic light emitting device according to the present invention may be an organic light emitting device having a structure 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 organic light emitting device of an inverted type 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.

FIG. 1 shows an example of an organic light emitting element composed of a substrate 1, an anode 2, a light emitting layer 3, and a cathode 4. As shown in FIG. In such a structure, the compound represented by Formula 1 may be included in the light emitting layer.

FIG. 2 shows an example of an organic light emitting element consisting of a substrate 1, an anode 2, a hole injection layer 5, a hole transport layer 6, a light emitting layer 7, an electron transport layer 8 and a cathode 4 It is. In such a structure, the compound represented by Chemical Formula 1 may be included in one or more layers of the hole injection layer, the hole transport layer, the light emitting layer and the electron transport layer.

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 layer of the organic material layer 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, by using a physical vapor deposition (PVD) method such as sputtering or e-beam evaporation, a metal or conductive metal oxide or an alloy thereof is deposited on the substrate to form an anode. In addition, an organic material layer including a hole injection layer, a hole transport layer, a light emitting layer, and an electron transport layer may be formed thereon, and then, a material that may be used as a cathode may be deposited thereon. In addition to the above 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 Chemical Formula 1 may be formed as an organic material layer by a solution coating method as well as a vacuum deposition method in the manufacture of the organic light emitting device. Here, the solution coating method means spin coating, dip coating, doctor blading, inkjet printing, screen printing, spray method, roll coating, etc., but is not limited thereto.

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

In one example, the first electrode is an anode, the second electrode is a cathode, or the first electrode is a cathode, the second electrode is an anode.

As the anode material, a material having a large work function is usually preferred to facilitate hole injection into the organic material layer. Specific examples of the positive electrode 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), indium zinc oxide (IZO); Combinations of oxides with metals such as ZnO: Al or SNO ₂ : Sb; Conductive polymers such as poly (3-methylthiophene), poly [3,4- (ethylene-1,2-dioxy) thiophene] (PEDOT), 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; Multilayer structure materials such as LiF / Al or LiO ₂ / Al, and the like, but are not limited thereto.

The hole injection layer is a layer for injecting holes from the electrode, and has a capability of transporting holes to the hole injection material, and has a hole injection effect at the anode, an excellent hole injection effect to the light emitting layer or the light emitting material, and is produced in the light emitting layer The compound which prevents the excitons from moving to the electron injection layer or the electron injection material, and is excellent in thin film formation ability is preferable. Preferably, the highest occupied molecular orbital (HOMO) 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 the hole injection material include metal porphyrin, oligothiophene, arylamine-based organic material, hexanitrile hexaazatriphenylene-based organic material, quinacridone-based organic material, and perylene-based Organic materials, anthraquinone, and 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, the hole transport material is a material capable of transporting holes from the anode or the hole injection layer to the light emitting layer. The material is suitable. Specific examples thereof include an arylamine-based organic material, a conductive polymer, and a block copolymer having a conjugated portion and a non-conjugated portion together, but are not limited thereto.

The light emitting material is a material capable of emitting light in the visible 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 with respect to fluorescence or phosphorescence is preferable. Specific examples thereof include 8-hydroxyquinoline aluminum complex (Alq ₃ ); Carbazole series compounds; Dimerized styryl compounds; BAlq; 10-hydroxybenzoquinoline-metal compound; Benzoxazole, benzthiazole and benzimidazole series compounds; Poly (p-phenylenevinylene) (PPV) -based polymers; Spiro compounds; Polyfluorene, rubrene and the like, but are not limited thereto.

The light emitting layer may include a host material and a dopant material as described above. The host material may further include a condensed aromatic ring derivative or a hetero ring-containing compound in addition to the compound represented by Formula 1 above. Specifically, the condensed aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, and fluoranthene compounds, and the heterocyclic containing compounds include carbazole derivatives, dibenzofuran derivatives and ladder types. Furan compounds, pyrimidine derivatives, and the like, but are not limited thereto.

Dopant materials include aromatic amine derivatives, styrylamine compounds, boron complexes, fluoranthene compounds, metal complexes, and the like. Specifically, the aromatic amine derivatives include condensed aromatic ring derivatives having a substituted or unsubstituted arylamino group, and include pyrene, anthracene, chrysene, and periplanthene having an arylamino group, and a styrylamine compound may be substituted or unsubstituted. At least one arylvinyl group is substituted with the arylamine, and 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, styrylamine, styryldiamine, styryltriamine, styryltetraamine and the like, but is not limited thereto. In addition, the metal complex includes, but is not limited to, an iridium complex, a platinum complex, and the like.

The electron transport layer is a layer that receives electrons from the electron injection layer and transports electrons to the light emitting layer. The electron transporting material is a material that can inject electrons well from the cathode and transfer them to the light emitting layer. Suitable. Specific examples include Al complexes of 8-hydroxyquinoline; Complexes including 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 in accordance with the prior art. In particular, examples of suitable cathode materials are conventional materials having a low work function followed by an aluminum or silver layer. Specifically cesium, barium, calcium, ytterbium and samarium, followed by aluminum layers or silver layers in each case.

The electron injection layer is a layer for injecting electrons from an electrode, has an ability of transporting electrons, has an electron injection effect from the cathode, an excellent electron injection effect to the light emitting layer or the light emitting material, and the hole injection of excitons generated in the light emitting layer The compound which prevents the movement to a layer and is excellent in thin film formation ability is preferable. Specifically, fluorenone, anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, preorenylidene methane, anthrone and the like and derivatives thereof, metal Complex compounds, nitrogen-containing five-membered ring derivatives, and the like, 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-naphtolato) aluminum, bis (2-methyl-8-quinolinato) (2-naphtolato) gallium, 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.

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

Synthesis Example

Synthesis Example 1 (Synthesis of Intermediate 1)

1-1) Synthesis of Intermediate 1-1

                                                    [Intermediate 1-1]

In a three-necked flask, 4,4,5,5-tetramethyl-2- (triphenylen-2-yl) -1,3,2-dioxaborolane (40.0 g, 112.9 mmol), 2-bromo-3-chlorophenol (24.6 g, 118.6 mmol) is dissolved in 1000 ml of THF and K ₂ CO ₃ (62.4 g, 451.6 mmol) is dissolved in 500 ml of H ₂ O. Here palladium-tetrakis (triphenylphosphine) (Pd (PPh ₃ ) ₄ ) (1.3 g, 1.1 mmol) was added and the mixture was stirred for 8 hours under argon atmosphere reflux conditions. After the reaction was completed, after cooling to room temperature, the reaction solution was transferred to a separatory funnel and extracted with CH ₂ Cl ₂ . The extract was dried over MgSO ₄ , filtered and concentrated, and the sample was purified by silica gel column chromatography to obtain 31.3 g of intermediate 1-1. (Yield 78%, MS [M + H] ⁺ = 354)

1-2) Synthesis of Intermediate 1

                                             [Intermediate 1]

Dissolve Intermediate 1-1 (30.0 g, 84.5 mmol) in 350 ml of Toluene in a three-neck flask, and add palladium (II) acetate (Pd (OAc) ₂ ) (0.9 g, 4.2 mmol), 1,3-bis ( 2,6-diisopropylphenyl) -1,3-dihydro-2H-imidazol-2-ylidene (IPr) (3.3 g, 8.5 mmol), sodium 2,4,6-trimethylbenzoate (MesCOONa) (7.9 g, 42.3 mmol), K ₂ CO ₃ (23.4 g, 169.1 mmol) and 0.5 ml of mesitylene were added sequentially, followed by stirring for 24 hours under reflux conditions of argon. After the reaction was completed, the mixture was cooled to room temperature, water was added thereto, and the reaction solution was transferred to a separatory funnel to extract with CH ₂ Cl ₂ . The extract was dried over MgSO ₄ , filtered and concentrated, and the sample was purified by silica gel column chromatography to obtain 16.7 g of intermediate 1. (Yield 56%, MS [M + H] ⁺ = 352)

Synthesis Example 2 (Synthesis of Intermediate 2)

2-1) Synthesis of Intermediate 2-1

                                                  [Intermediate 2-1]

4 triphenylen-2-ol (30.0 g, 122.8 mmol), 2-bromo-1-chloro-3-fluorobenzene (27.0 g, 128.9 mmol) and K ₂ CO ₃ (25.5 g, 184.2 mmol) and dissolved in 500 ml of DMAc, and stirred for 12 hours under reflux conditions. After the reaction was completed, the reaction mixture was cooled to room temperature, water was added thereto, and the reaction solution was transferred to a separatory funnel and extracted with ethyl acetate. The extract was purified by silica gel column chromatography to give 39.9 g of intermediate 2-1. (Yield 75%, MS [M + H] ⁺ = 433)

2-2) Synthesis of Intermediate 2

                                            [Intermediate 2]

Intermediate 2-1 (30.0 g, 102.5 mmol), palladium (II) acetate (Pd (OAc) ₂ ) (1.2 g, 5.1 mmol), tricyclohexylphosphine (2.9 g, 10.2 mmol), K ₂ CO ₃ ( 42.5 g, 307.5 mmol) and 425 ml of DMAc were added and stirred for 24 hours under reflux conditions under argon. After the reaction was completed, the mixture was cooled to room temperature, water was added thereto, and the reaction solution was transferred to a separatory funnel to extract with CH ₂ Cl ₂ . The extract was dried over MgSO ₄ , filtered and concentrated, and the sample was purified by silica gel column chromatography to obtain 15.2 g of intermediate 2. (Yield 42%, MS [M + H] ⁺ = 352)

Synthesis Example 3 (Synthesis of Compound 1)

[Intermediate 1] [Intermediate A] [Compound 1]

In a three-necked flask, intermediate 1 (10.0 g, 28.3 mmol) and intermediate A (12.2 g, 34.0 mmol) obtained in Synthesis Example 1 were dissolved in 285 ml of THF and K ₂ CO ₃ (15.7 g, 113.4 mmol) is dissolved in 142 ml of H ₂ O. Palladium-tetrakis (triphenylphosphine) (Pd (PPh ₃ ) ₄ ) (0.3 g, 0.3 mmol) was added thereto, and the mixture was stirred for 8 hours under reflux conditions under argon. After the reaction was completed, after cooling to room temperature, the reaction solution was transferred to a separatory funnel and extracted with CH ₂ Cl ₂ . After the extract was dried over MgSO ₄ , filtered and concentrated, the sample was purified by silica gel column chromatography, and then 5.3 g of Compound 1 was obtained through a sublimation tablet. (Yield 34%, MS [M + H] ⁺ = 549)

Synthesis Example 4 (Synthesis of Compound 2)

  [Intermediate 1] [Intermediate B] [Compound 2]

Compound 2 was synthesized in the same manner as in the synthesis of Compound 1, except that Intermediate A was used as Intermediate B in <Synthesis Example 3>. (MS [M + H] ⁺ = 639)

Synthesis Example 5 (Synthesis of Compound 3)

[중간체 1] [중간체 C] [화합물 3]

[Intermediate 1] [Intermediate C] [Compound 3]

Compound 3 was synthesized in the same manner as in the synthesis of Compound 1, except that Intermediate A was used as Intermediate C in <Synthesis Example 3>. (MS [M + H] ⁺ = 625)

Synthesis Example 6 (Synthesis of Compound 4)

   [Intermediate 1] [Intermediate D] [Compound 4]

Compound 4 was synthesized in the same manner as in the synthesis of Compound 1, except that Intermediate A was used as Intermediate D in <Synthesis Example 3>. (MS [M + H] ⁺ = 625)

Synthesis Example 7 (Synthesis of Compound 5)

[Intermediate 2] [Intermediate A] [Compound 5]

A compound 5 was synthesized in the same manner as in the synthesis of compound 1, except that Intermediate 1 in <Synthesis Example 3> was used as Intermediate 2 obtained in <Synthesis Example 2>. (MS [M + H] ⁺ = 549)

Synthesis Example 8 (Synthesis of Compound 6)

[Intermediate 2] [Intermediate B] [Compound 6]

Compound 6 was synthesized in the same manner as in the synthesis of Compound 1, except that Intermediate 1 was changed to Intermediate 2, and Intermediate A to Intermediate B in <Synthesis Example 3>. (MS [M + H] ⁺ = 639)

Synthesis Example 9 (Synthesis of Compound 7)

[Intermediate 2] [Intermediate D] [Compound 7]

Compound 7 was synthesized in the same manner as in the synthesis of Compound 1, except that Intermediate 1 was used as Intermediate 2, and Intermediate A was changed to Intermediate D in <Synthesis Example 3>. (MS [M + H] ⁺ = 625)

EXAMPLE

<Example 1>

A glass substrate coated with a thin film of ITO (Indium Tin Oxide) having a thickness of 1,400 kPa was put in distilled water in which detergent was dissolved and ultrasonically cleaned. At this time, Fischer Co. product was used as a detergent, and distilled water filtered secondly as a filter of Millipore Co. product was used as distilled water. After ITO was washed for 30 minutes, ultrasonic washing was performed twice with distilled water for 10 minutes. After washing the distilled water, ultrasonic washing with a solvent of isopropyl alcohol, acetone, methanol, dried and transported to a plasma cleaner. In addition, the substrate was cleaned for 5 minutes using an oxygen plasma, and then the substrate was transferred to a vacuum evaporator.

The HT-A 95 wt% and the P-DOPANT 5 wt% on the ITO transparent electrode thus prepared, thermal vacuum deposition at a thickness of 100 kPa and then only HT-A material was deposited to a thickness of 1150 kPa to form a hole transport layer.

[HT-A] [P-DOPANT]

The following HT-B was heat-vacuum-deposited at 450 micrometer thickness on it as an electronic blocking layer.

[HT-B]

Subsequently, thermal vacuum deposition was carried out at a ratio of 47 wt% of the following compound 1 as the first host material of the light emitting layer, 47 wt% of the following GH as the second host material, 6 wt% of the following GD as the dopant material, and 400 kPa thick.

[Compound 1] [GH] [GD]

Subsequently, the following ET-A was thermally vacuum deposited to a thickness of 50 kPa as the hole blocking layer.

[ET-A]

Subsequently, the following ET-B and Liq were thermally vacuum deposited at a thickness of 250 kPa in a 2: 1 ratio, and then LiF and magnesium were vacuum deposited at a thickness of 30 kPa in a ratio of 1: 1 as an electron transport and injection layer.

[ET-B] [Liq]

Magnesium and silver were deposited on the electron injection layer at a thickness of 160 로 at a ratio of 1: 4 to form a cathode to manufacture an organic light emitting device.

<Examples 2 to 7 and Comparative Examples 1 to 4>

The organic light emitting diodes of Examples 2 to 7 and Comparative Examples 1 to 4 were manufactured by using the same method as Example 1, except that the first host material was changed as shown in Table 1 below. .

Current was applied to the organic light emitting diodes manufactured in Examples 1 to 7 and Comparative Examples 1 to 4, and voltage, efficiency, and lifetime (T95) were measured, and the results are shown in Table 1 below. At this time, the voltage, efficiency was measured by applying a current density of 10mA / cm ² , T95 means the time until the initial luminance to 95% at a current density of 20mA / cm ² .

Host 1
matter @ 10mA / cm ² @ 20mA / cm ² Voltage
(V) efficiency
(cd / A) life span
(T95, hr) Example 1 Compound 1 4.3 65.5 130 Example 2 Compound 2 4.4 62.1 130 Example 3 Compound 3 4.4 61.4 110 Example 4 Compound 4 4.3 63.2 140 Example 5 Compound 5 4.4 64.3 130 Example 6 Compound 6 4.5 63.7 120 Example 7 Compound 7 4.4 64.5 130 Comparative Example 1 GH-A 4.5 42.1 80 Comparative Example 2 GH-B 4.8 43.5 70 Comparative Example 3 GH-C 4.6 44.8 50 Comparative Example 4 GH-D 4.9 40.8 20

[GH-A] [GH-B]

[GH-C] [GH-D]

From the results of Table 1, when the compound represented by Chemical Formula 1 (compounds 1 to 7 of Examples 1 to 7) is applied as the light emitting layer host of the organic EL device, it was confirmed that a high luminous efficiency and a long life device can be obtained. .

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

Claims (6)

A compound represented by the following formula 1-1 or 1-2:
[Formula 1-1]

In Chemical Formula 1-1,
X is O or S,
R ₄ is hydrogen,
R ₅ is combined with * in Formula 3,
[Formula 1-2]

In Chemical Formula 1-2,
X is O or S,
One of R ₄ and R ₅ is bonded with * in Formula 3, and the other is hydrogen;
[Formula 3]

In Chemical Formula 3,
L is a bond, phenylene, biphenylene, or naphthylene,
Z are each independently N, or CH, provided that at least one of Z is N,
Ar ₁ and Ar ₂ are each independently C _6-60 aryl; Or C _2-60 heteroaryl containing one or more heteroatoms selected from the group consisting of O, N, Si and S.
delete The method of claim 1,
L is a bond, or phenylene,
compound.
The method of claim 1,
Ar ₁ and Ar ₂ are each independently phenyl, biphenylyl, terphenylyl, dimethylfluorenyl, naphthyl, pyridinyl, dibenzofuranyl, or dibenzothiophenyl,
compound.
The method of claim 1,
The compound is any one selected from the group consisting of the following compounds:

.
A first electrode; A second electrode provided to face the first electrode; And at least one organic material layer provided between the first electrode and the second electrode, wherein at least one of the organic material layers is any one of claims 1 and 3 to 5. It comprises a compound according to, organic light emitting device.

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