KR20150037318A - Hetero-cyclic compound and organic light emitting device comprising the same - Google Patents

Abstract

The present invention provides a heterocyclic compound and an organic light emitting device comprising the heterocyclic compound.

Description

HETERO-CYCLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME [0002]

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

In general, organic light emission phenomenon refers to a phenomenon in which an organic material is used to convert electric energy into light energy. An organic light emitting device using an organic light emitting phenomenon generally has a structure including an anode, a cathode, and an organic material layer therebetween. Here, in order to increase the efficiency and stability of the organic light emitting device, the organic material layer may have a multi-layer structure composed of different materials and may include a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, and an electron injection layer. When a voltage is applied between the two electrodes in the structure of such an organic light emitting device, holes are injected in the anode, electrons are injected into the organic layer in the cathode, excitons are formed when injected holes and electrons meet, When it falls back to the ground state, the light comes out.

Development of new materials for such organic light emitting devices has been continuously required.

Tang, C. W .; VanSlyke, S. A .; Chen, C. H., Electroluminescence of doped organic thin films, Journal of Applied Physics (1989), 65 (9), 3610-16.

It is an object of the present invention to provide a heterocyclic compound and an organic light emitting device including the heterocyclic compound.

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

[Chemical Formula 1]

In formula (1)

X1 to X3 are the same or different from each other and are each CH or N,

At least one of X1 to X3 is N,

X4 to X6 are the same or different and each is CH or N,

At least one of X4 to X6 is N,

Ar 1 to Ar 4 are the same or different and are each independently a substituted or unsubstituted aryl group.

In addition, in one embodiment of the present specification, the first electrode; A second electrode facing the first electrode; And at least one organic layer including a light emitting layer provided between the first electrode and the second electrode,

Wherein at least one of the organic material layers comprises a heterocyclic compound represented by the general formula (1).

The novel compound according to the present invention can be used as a material for an organic material layer of an organic light emitting device including an organic light emitting device. By using the new compound, it is possible to improve the efficiency, the driving voltage and / or the lifetime characteristics of the organic light emitting device.

1 to 5 are cross-sectional views illustrating the structure of an organic light emitting device according to an embodiment of the present invention.

Hereinafter, the present specification will be described in detail.

The present invention provides a compound represented by the above formula (1).

In the present specification, the compound represented by the formula (1) has a monocyclic heterocyclic group containing at least one N atom on both sides of a 1,4-naphthalene group, that is, a heterocyclic ring containing X1 to X3 or X4 to X6, .

The present specification can have properties suitable for use as an organic material layer used in an organic light emitting device by introducing a substituent including a heterocycle on both sides of a naphthalene group. By selecting a compound having an appropriate energy level according to a substituent and using it as an electron injecting and / or electron transporting material in the organic light emitting device, the energy band gap can be finely adjusted and the characteristics can be improved.

In the case of the 1,4-naphthalene group, the driving voltage is lower than that of the 1,5-naphthalene group or the 2,6-naphthalene group, and a device having high light efficiency can be realized.

When they are connected to each other through a phenylene group, their molecular weights are higher than those of compounds directly bonded to naphthalene, so that the glass transition temperature (Tg) is high and the thermal stability is excellent. Such an increase in thermal stability in an organic light emitting device provides driving stability to the device, thereby improving lifetime characteristics. Also, compounds having various energy bandgaps can be synthesized by controlling the HOMO and LUMO energy levels and / or conjugation length of a compound by introducing various substituent groups into the phenylene group. Since naphthalene serves as an electron donor and substituents serve as electron acceptors, the obital distribution in the Obital distribution of HOMO and LUMO is desirable when there is a certain distance between the two units, The device characteristics are improved as compared with the case of directly bonding.

Illustrative examples of such substituents are set forth below, but are not limited thereto.

As used herein, the term "substituted or unsubstituted" A halogen group; A nitrile group; A nitro group; A hydroxy group; A substituted or unsubstituted alkyl group; A substituted or unsubstituted cycloalkyl group; A substituted or unsubstituted alkenyl group; A substituted or unsubstituted amine group; A substituted or unsubstituted alkylamine group; A substituted or unsubstituted aralkylamine group; A substituted or unsubstituted arylamine group; A substituted or unsubstituted heteroarylamine group; A substituted or unsubstituted aryl group; A substituted or unsubstituted fluorenyl group; A substituted or unsubstituted carbazole group; And a substituted or unsubstituted heterocyclic group containing at least one of N, O and S atoms, or has no substituent group.

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 50. Specific examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec- N-pentyl, 3-dimethylbutyl, 2-ethylbutyl, heptyl, n-hexyl, N-octyl, 2-ethylhexyl, 2-propylpentyl, n-nonyl, 2,2-dimethyl Heptyl, 1-ethyl-propyl, 1,1-dimethyl-propyl, isohexyl, 2-methylpentyl, 4-methylhexyl, 5-methylhexyl and the like.

In the present specification, the cycloalkyl group is not particularly limited, but preferably has 3 to 60 carbon atoms, and specifically includes cyclopropyl, cyclobutyl, cyclopentyl, 3-methylcyclopentyl, 2,3-dimethylcyclopentyl, cyclohexyl, But are not limited to, 3-methylcyclohexyl, 4-methylcyclohexyl, 2,3-dimethylcyclohexyl, 3,4,5-trimethylcyclohexyl, 4-tert- butylcyclohexyl, cycloheptyl, Do not.

In the present specification, the alkenyl group may be straight-chain or branched, and the number of carbon atoms is not particularly limited, but is preferably 2 to 40. Specific examples include vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, Butenyl, allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, (Diphenyl-1-yl) vinyl-1-yl, stilbenyl, stilenyl, and the like.

In the present specification, the aryl group may be a monocyclic aryl group or a polycyclic aryl group, and includes a case where an alkyl group having 1 to 25 carbon atoms or an alkoxy group having 1 to 25 carbon atoms is substituted. In addition, an aryl group in the present specification may mean an aromatic ring.

When the aryl group is a monocyclic aryl group, the number of carbon atoms is not particularly limited, but is preferably 6 to 25 carbon atoms. Specific examples of the monocyclic aryl group include, but are not limited to, a phenyl group, a biphenyl group, a terphenyl group, and a stilbenyl group.

When the aryl group is a polycyclic aryl group, the number of carbon atoms is not particularly limited. And preferably has 10 to 24 carbon atoms. Specific examples of the polycyclic aryl group include naphthyl, anthracenyl, phenanthryl, pyrenyl, perylenyl, klychenyl, fluorenyl, and the like.

In the present specification, a fluorenyl group is a structure in which two cyclic organic compounds are connected through one atom.

The fluorenyl group includes a structure of an open fluorenyl group, wherein the open fluorenyl group is a structure in which one ring compound is disconnected in a structure in which two ring organic compounds are connected through one atom.

,

,

및

등이 될 수 있다. 다만, 이에 한정되는 것은 아니다.When the fluorenyl group is substituted,

,

,

And

And the like. However, the present invention is not limited thereto.

In the present specification, the heterocyclic group is a heterocyclic group containing at least one of O, N and S as a heteroatom. The number of carbon atoms is not particularly limited, but is preferably 2 to 60 carbon atoms. Examples of the heterocyclic group include a thiophene group, a furane group, a furyl group, an imidazole group, a thiazole group, an oxazole group, an oxadiazole group, a triazole group, a pyridyl group, a bipyridyl group, a pyrimidyl group, A pyridazinyl group, a pyrazinopyrazinyl group, an isoquinoline group, a pyrazinyl group, a pyrazinyl group, a pyrazinyl group, a pyrazinyl group, a quinolinyl group, a quinazolinyl group, a quinoxalinyl group, a phthalazinyl group, a pyridopyrimidinyl group, , An indole group, a carbazole group, a benzooxazole group, a benzoimidazole group, a benzothiazole group, a benzocarbazole group, a benzothiophene group, a dibenzothiophene group, a benzofuranyl group, a phenanthroline, An isoxazolyl group, an oxadiazolyl group, a thiadiazolyl group, a benzothiazolyl group, a phenothiazinyl group, and a dibenzofuranyl group, but is not limited thereto.

In the present specification, the number of carbon atoms of the amine group is not particularly limited, but is preferably 1 to 30. Specific examples of the amine group include a methylamine group, a dimethylamine group, an ethylamine group, a diethylamine group, a phenylamine group, a naphthylamine group, a biphenylamine group, an anthracenylamine group, a 9- , A diphenylamine group, a phenylnaphthylamine group, a ditolylamine group, a phenyltolylamine group, a triphenylamine group, and the like, but are not limited thereto.

In the present specification, examples of the arylamine group include a substituted or unsubstituted monoarylamine group, a substituted or unsubstituted diarylamine group, or a substituted or unsubstituted triarylamine group. The aryl group in the arylamine group may be a monocyclic aryl group or a polycyclic aryl group. The arylamine group having at least two aryl groups may contain a monocyclic aryl group, a polycyclic aryl group, or a monocyclic aryl group and a polycyclic aryl group at the same time.

Specific examples of the arylamine group include phenylamine, naphthylamine, biphenylamine, anthracenylamine, 3-methylphenylamine, 4-methyl-naphthylamine, 2-methyl- But are not limited to, cenylamine, diphenylamine, phenylnaphthylamine, ditolylamine, phenyltolylamine, carbazole and triphenylamine groups.

In the present specification, the heteroaryl group in the heteroarylamine group can be selected from the examples of the above-mentioned heterocyclic group.

이다. In one embodiment of the present invention, the phenylene group connecting the hetero ring containing X 1 to X 3 with naphthalene is

to be.

이다. In one embodiment of the present invention, the phenylene group connecting the hetero ring containing X 1 to X 3 with naphthalene is

to be.

이다. In one embodiment of the present invention, the phenylene group connecting the hetero ring containing X 1 to X 3 with naphthalene is

to be.

이다. In one embodiment of the present invention, the phenylene group connecting the hetero ring containing X4 to X6 to naphthalene is

to be.

이다. In one embodiment of the present invention, the phenylene group connecting the hetero ring containing X4 to X6 to naphthalene is

to be.

이다. In one embodiment of the present invention, the phenylene group connecting the hetero ring containing X4 to X6 to naphthalene is

to be.

는 다른 치환기에 연결되는 부위를 의미한다.In the present specification,

Quot; refers to a moiety that is connected to another substituent.

In one embodiment of the present invention, the heterocyclic compound represented by Formula 1 is represented by any one of Chemical Formulas 2 to 7 below.

(2)

(3)

[Chemical Formula 4]

[Chemical Formula 5]

[Chemical Formula 6]

(7)

In formulas (2) to (7)

Ar1 to Ar4 and X1 to X6 are the same as defined in claim 1.

In one embodiment of the present invention, X 1 to X 3 are the same or different from each other, and each independently N or CH, and at least one of X 1 to X 3 is N.

In one embodiment of the present disclosure, X1 to X3 are N.

In one embodiment of the present disclosure, X1 may be N, and X2 and X3 may be CH.

In one embodiment of the present disclosure, X2 may be N, and X1 and X3 may be CH.

In one embodiment of the present disclosure, X3 is N, and X1 and X2 may be CH.

In one embodiment of the present disclosure, X1 and X2 may be N. In this case, X3 is CH.

In one embodiment of the present disclosure, X1 and X3 may be N. In this case, X2 is CH.

In one embodiment of the present disclosure, X2 and X3 may be N. In this case, X1 is CH.

In one embodiment of the present invention, X4 to X6 are the same or different from each other, and each independently N or CH, and at least one of X4 to X6 is N.

In one embodiment of the present disclosure, X4 to X6 are N.

In one embodiment of the present disclosure, X4 is N and X5 and X6 may be CH.

In one embodiment of the present disclosure, X5 may be N, and X4 and X6 may be CH.

In one embodiment of the present disclosure, X6 is N and X4 and X5 may be CH.

In one embodiment of the present disclosure, X4 and X5 may be N. In this case, X6 is CH.

In one embodiment of the present disclosure, X4 and X6 may be N. [ In this case, X5 is CH.

In one embodiment of the present disclosure, X5 and X6 may be N. In this case, X4 is CH.

In one embodiment of the present invention, Ar 1 to Ar 4 are the same or different and are each independently a substituted or unsubstituted aryl group.

In one embodiment of the present invention, Ar1 to Ar4 are the same or different and each independently represents a substituted or unsubstituted phenyl group; Or a substituted or unsubstituted biphenyl group.

In one embodiment of the present invention, Ar1 to Ar4 are the same or different from each other and are each independently a phenyl group or a biphenyl group.

In one embodiment of the present specification, Ar1 is a substituted or unsubstituted aryl group.

In one embodiment of the present invention, Ar1 is a substituted or unsubstituted phenyl group.

In one embodiment of the present invention, Ar1 is a phenyl group.

In one embodiment of the present specification, Ar1 is a substituted or unsubstituted biphenyl group.

In one embodiment of the present invention, Ar1 is a biphenyl group.

In one embodiment of the present specification, Ar2 is a substituted or unsubstituted aryl group.

In one embodiment of the present invention, Ar2 is a substituted or unsubstituted phenyl group.

In one embodiment of the present specification, Ar2 is a phenyl group.

In one embodiment of the present specification, Ar2 is a substituted or unsubstituted biphenyl group.

In one embodiment of the present specification, Ar2 is a biphenyl group.

In one embodiment of the present specification, Ar3 is a substituted or unsubstituted aryl group.

In one embodiment of the present invention, Ar3 is a substituted or unsubstituted phenyl group.

In one embodiment of the present specification, Ar3 is a phenyl group.

In one embodiment of the present specification, Ar3 is a substituted or unsubstituted biphenyl group.

In one embodiment of the present specification, Ar3 is a biphenyl group.

In one embodiment of the present specification, Ar4 is a substituted or unsubstituted aryl group.

In one embodiment of the present invention, Ar4 is a substituted or unsubstituted phenyl group.

In one embodiment of the present specification, Ar4 is a phenyl group.

In one embodiment of the present specification, Ar4 is a substituted or unsubstituted biphenyl group.

In one embodiment of the present specification, Ar4 is a biphenyl group.

In one embodiment of the present invention, the heterocyclic compound represented by Formula 1 is any one of the following Formulas 2-1 to 2-32.

In one embodiment of the present invention, the heterocyclic compound represented by Formula 1 is any one of the following Formulas 3-1 to 3-32.

In one embodiment of the present invention, the heterocyclic ring compound represented by Formula 1 is any one of the following Formulas 4-1 to 4-32.

In one embodiment of the present invention, the heterocyclic compound represented by the formula (1) is any one of the following formulas (5-1) to (5-50).

In one embodiment of the present invention, the heterocyclic compound represented by Formula 1 is any one of the following Formulas 6-1 to 6-50.

In one embodiment of the present invention, the heterocyclic compound represented by the formula (1) is any one of the following formulas (7-1) to (7-50).

The compound of formula (1) may be prepared based on the preparation examples described below.

The compound represented by Formula 1 is obtained by linking phenylene groups in the ortho, meta and / or para directions on both sides of a 1,4-naphthalene group, substituting X1 to X3 and substituting Ar1 and Ar2 And a heterocyclic ring containing X4 to X6 and substituted with Ar3 and Ar4, respectively.

2-1 to 2-32, 3-1 to 3-32, 4-1 to 4-32, 5-1 to 5-50, and 5-1 to 5-50 by changing the number of heteroatoms of X1 to X6 and the substituents of Ar1 to Ar4, 6-1 to 6-50 and 7-1 to 7-50, as well as the heterocyclic compound represented by the formula (1).

The present invention also provides an organic light emitting device comprising the heterocyclic compound represented by Formula 1.

In one embodiment of the present disclosure, the first electrode; A second electrode facing the first electrode; And at least one organic material layer including a light emitting layer disposed between the first electrode and the second electrode, wherein at least one of the organic material layers includes the heterocyclic compound, to provide.

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 injecting layer, a hole transporting layer, a light emitting layer, an electron transporting layer, and an electron injecting layer 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 one embodiment of the present invention, the organic material layer includes a hole transport layer, a hole injection layer, or a layer simultaneously injecting holes and transporting holes,

The hole transporting layer, the hole injecting layer, or the layer that simultaneously injects holes and transports holes includes the heterocyclic compound.

In another embodiment, the light emitting layer comprises the heterocyclic compound.

In one embodiment of the present invention, the organic material layer includes an electron transporting layer, an electron injecting layer, or a layer simultaneously performing electron transport and electron injection,

The electron transporting layer, the electron injecting layer, or the layer that simultaneously transports electrons and injects electrons includes the above heterocyclic compound.

In one embodiment of the present invention, the electron transporting layer, the electron injection layer, or the layer which simultaneously transports electrons and electron injection contains only the heterocyclic compound.

In one embodiment of the present invention, the organic material layer further includes a hole injection layer or a hole transport layer containing a compound including an arylamino group, a carbazole group or a benzocarbazole group in addition to the organic compound layer including the heterocyclic compound.

In one embodiment of the present invention, the organic compound layer containing the heterocyclic compound includes the heterocyclic compound as a host and includes another organic compound, metal or metal compound as a dopant.

In one embodiment of the present invention, the organic layer includes a hole blocking layer, and the hole blocking layer includes the heterocyclic compound.

In one embodiment of the present invention, the organic material layer is a hole injection layer, a hole transport layer. An electron transport layer, an electron injection layer, an electron blocking layer, and a hole blocking layer.

In another embodiment, the organic light emitting device may be a normal type organic light emitting device in which an anode, at least one organic layer, and a cathode are sequentially stacked on a substrate.

 In another embodiment, the organic light emitting device may be an inverted type organic light emitting device in which a cathode, at least one organic material layer, and an anode are sequentially stacked on a substrate.

For example, the structure of the organic light emitting device according to the present invention is illustrated in FIGS.

FIG. 1 illustrates the structure of an organic light emitting device in which an anode 2, a light emitting layer 5, and a cathode 7 are sequentially stacked on a substrate 1. In such a structure, the compound represented by Formula 1 may be included in the light emitting layer 5.

2 illustrates the structure of an organic light emitting device in which an anode 2, a light emitting layer 5, an electron transport layer 6, and a cathode 7 are sequentially laminated on a substrate 1. In FIG. In such a structure, the compound represented by Formula 1 may be included in the light-emitting layer 5 or the electron-transporting layer 6.

3 illustrates a structure of an organic light emitting device in which an anode 2, a hole transporting layer 4, a light emitting layer 5, an electron transporting layer 6, and a cathode 7 are sequentially laminated on a substrate 1. In such a structure, the compound represented by Formula 1 may be included in the hole transport layer 4, the light emitting layer 5, or the electron transport layer 6.

4 illustrates the structure of an organic light emitting device in which an anode 2, a hole injecting layer 3, a hole transporting layer 4, a light emitting layer 5, and a cathode 7 are sequentially stacked on a substrate 1. In such a structure, the compound represented by Formula 1 may be included in the hole injecting layer 3, the hole transporting layer 4, or the electron transporting layer 6.

5 shows an organic light emitting device in which an anode 2, a hole injecting layer 3, a hole transporting layer 4, a light emitting layer 5, an electron transporting layer 6 and a cathode 7 are sequentially laminated on a substrate 1 Structure is illustrated. In such a structure, the compound represented by Formula 1 may be included in the hole injecting layer 3, the hole transporting layer 4, the light emitting layer 5, or the electron transporting layer 6.

The organic light-emitting device of the present invention can be manufactured by materials and methods known in the art, except that one or more of the organic layers includes the compound of the present invention, i.e., the heterocyclic compound.

When the organic light emitting diode includes a plurality of organic layers, the organic layers may be formed of the same material or different materials.

 The organic light emitting device of the present invention can be manufactured by materials and methods known in the art, except that one or more of the organic layers include the heterocyclic compound, i.e., the compound represented by Formula 1 above.

For example, the organic light emitting device of the present invention can be manufactured by sequentially laminating a first electrode, an organic material layer, and a second electrode on a substrate. At this time, by using a PVD (physical vapor deposition) method such as a sputtering method or an e-beam evaporation method, a metal or a metal oxide having conductivity or an alloy thereof is deposited on the substrate to form a positive electrode Forming an organic material layer including a hole injecting layer, a hole transporting layer, a light emitting layer and an electron transporting layer thereon, and depositing a material usable as a cathode thereon. In addition to such a method, an organic light emitting device can be formed by sequentially depositing a cathode material, an organic material layer, and a cathode material on a substrate.

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

In addition to such a method, an organic light emitting device may be fabricated by sequentially depositing an organic material layer and a cathode material on a substrate from a cathode material (International Patent Application Publication No. 2003/012890). However, the manufacturing method is not limited thereto.

In one embodiment of the present invention, the first electrode is an anode and the second electrode is a cathode.

In another embodiment, the first electrode is a cathode and the second electrode is a cathode.

As the anode material, a material having a large work function is preferably used so that hole injection can be smoothly conducted into the organic material layer. Specific examples of the cathode material that can be used in the present invention 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); ZnO: Al or SNO _2: a combination of a metal and an oxide such as Sb; Conductive polymers such as poly (3-methylthiophene), poly [3,4- (ethylene-1,2-dioxy) thiophene] (PEDOT), polypyrrole and polyaniline.

The negative electrode material is preferably 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; Layer structure materials such as LiF / Al or LiO ₂ / Al, but are not limited thereto.

The hole injecting material is a layer for injecting holes from the electrode. The hole injecting material has a hole injecting effect, a hole injecting effect in the anode, and an excellent hole injecting effect in the light emitting layer or the light emitting material. A compound which prevents the exciton from migrating to the electron injection layer or the electron injection material and is also excellent in the thin film forming ability is preferable. It is preferable that the highest occupied molecular orbital (HOMO) of the hole injecting material be between the work function of the anode material and the HOMO of the surrounding organic layer. Specific examples of the hole injecting material include metal porphyrin, oligothiophene, arylamine-based organic materials, hexanitrile hexaazatriphenylene-based organic materials, quinacridone-based organic materials, and perylene- , Anthraquinone, polyaniline and polythiophene-based conductive polymers, but the present invention is not limited thereto.

The hole transport layer is a layer that transports holes from the hole injection layer to the light emitting layer. 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 include arylamine-based organic materials, conductive polymers, and block copolymers having a conjugated portion and a non-conjugated portion together, but are not limited thereto.

The light emitting material is preferably a material capable of emitting light in the visible light region by transporting and receiving holes and electrons from the hole transporting layer and the electron transporting layer, respectively, and having good quantum efficiency for fluorescence or phosphorescence. Specific examples include 8-hydroxy-quinoline aluminum complex (Alq ₃ ); Carbazole-based compounds; Dimerized styryl compounds; BAlq; 10-hydroxybenzoquinoline-metal compounds; Compounds of the benzoxazole, benzothiazole and benzimidazole series; Polymers of poly (p-phenylenevinylene) (PPV) series; 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. The host material is a condensed aromatic ring derivative or a heterocyclic compound. Specific examples of the condensed aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, and fluoranthene compounds. Examples of the heterocycle-containing compounds include carbazole derivatives, dibenzofuran derivatives, Furan compounds, pyrimidine derivatives, and the like, but are not limited thereto.

The dopant material includes an organic compound, a metal, or a metal compound.

Examples of the organic compound as the dopant material include an aromatic amine derivative, a styrylamine compound, a boron complex, and a fluoranthene compound. Specific examples of the aromatic amine derivatives include condensed aromatic ring derivatives having substituted or unsubstituted arylamino groups, and examples thereof include pyrene, anthracene, chrysene, and peripherrhene having an arylamino group. Examples of the styrylamine compound include substituted or unsubstituted Wherein at least one aryl vinyl group is substituted with at least one aryl vinyl group, and at least one substituent selected from the group consisting of an aryl group, a silyl group, an alkyl group, a cycloalkyl group and an arylamino group is substituted or unsubstituted. Specific examples thereof include, but are not limited to, styrylamine, styryldiamine, styryltriamine, styryltetraamine, and the like. As the metal or metal compound, a common metal or metal compound can be used. Specifically, metal complexes can be used. Examples of the metal complex include iridium complex, platinum complex, and the like, but are not limited thereto.

The electron transporting material is a layer that receives electrons from the electron injecting layer and transports electrons to the light emitting layer. The electron transporting material is a material capable of transferring electrons from the cathode well to the light emitting layer. Is suitable. Specific examples include an Al complex of 8-hydroxyquinoline; Complexes containing Alq3; Organic radical compounds; Hydroxyflavone-metal complexes, and the like, but are not limited thereto. The electron transporting layer can be used with any desired cathode material as used according to the prior art. In particular, an example of a suitable cathode material is a conventional material having a low work function followed by an aluminum layer or a silver layer. Specifically cesium, barium, calcium, ytterbium and samarium, in each case followed by an aluminum layer or a silver layer.

The electron injection layer is a layer for injecting electrons from the electrode. The electron injection layer has an ability to transport electrons, has an electron injection effect from the cathode, and has an excellent electron injection effect with respect to the light emitting layer or the light emitting material. A compound which prevents migration to a layer and is excellent in a thin film forming ability is preferable. Specific examples thereof include fluorenone, anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, preorenylidene methane, A complex compound and a nitrogen-containing five-membered ring derivative, 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- Tris (8-hydroxyquinolinato) aluminum, tris (2-methyl-8-hydroxyquinolinato) aluminum, tris (8- hydroxyquinolinato) gallium, bis (10- Quinolinato) beryllium, bis (10-hydroxybenzo [h] quinolinato) zinc, bis (2-methyl-8- quinolinato) chlorogallium, bis (2-methyl-8-quinolinato) (2-naphtholato) gallium, and the like, But is not limited thereto.

The hole blocking layer prevents holes from reaching the cathode, and may be formed under the same conditions as those of the hole injecting layer. Specific examples thereof include, but are not limited to, oxadiazole derivatives, triazole derivatives, phenanthroline derivatives, BCP, aluminum complexes and the like.

The organic light emitting device according to the present invention may be of a top emission type, a back emission type, or a both-side emission type, depending on the material used.

In one embodiment of the present invention, the heterocyclic compound may be included in an organic solar cell or an organic transistor in addition to an organic light emitting device.

The heterocyclic 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 intended to illustrate the present specification, and the scope of the present specification is not limited thereto.

Manufacturing example

< Manufacturing example  1> Preparation of the following compound 2-1

1) Synthesis of the following compound 1-A

[Compound 1-A]

A suspension was prepared by suspending magnesium (19.4 g, 0.8 mol) and iodine (2.04 g, 16 mmol) in anhydrous tetrahydrofuran in a 160 ml solvent in a nitrogen atmosphere, and bromobenzene (125.6 g, 0.8 mol) was suspended in anhydrous tetrahydrofuran A solution diluted to 300 ml was slowly added dropwise to the suspension over 1 hour, and the mixture was heated to reflux for 5 hours. After the mixture was cooled to room temperature, a solution of 1,3,5-trichlorotriazine (55.2 g, 0.3 mol) in 300 ml of anhydrous tetrahydrofuran was slowly added dropwise to the mixture, and the mixture was refluxed for about 7 hours. After completion of the reaction, the organic solvent of the reaction fluid was distilled off under reduced pressure and then recrystallized from ethanol to obtain Compound 1-A (78 g, yield: 73.5%).

MS [M + H] &lt; ⁺ &gt; = 268

2) Synthesis of the following compound 1-B

[Compound 1-A] [Compound 1-B]

The compound 1-A (55.65 g, 0.21 mol) and 4-chlorophenylboronic acid (35.7 g, 0.23 mol) were completely dissolved in 240 ml of tetrahydrofuran in a nitrogen atmosphere, and 2M aqueous potassium carbonate solution (120 ml) And tetrakis- (triphenylphosphine) palladium (4.8 g, 4.1 mmol) were added thereto, followed by heating and stirring for 7 hours. The temperature was lowered to room temperature, and the water layer was removed. The organic layer was dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and then subjected to column chromatography with tetrahydrofuran: hexane = 1: 6 to prepare the compound 1-B (51 g, yield: 72%).

MS [M + H] &lt; ⁺ &gt; = 344

3) Synthesis of the following compound 1-C

[Compound 1-B] [Compound 1-C]

(51.4 g, 148.4 mmol), bis (pinacolato) diboron (41.4 g, 162 mmol) and potassium acetate (43.7 g, 444 mmol) were added to 150 ml of dioxane and heated with stirring in a nitrogen atmosphere . Bis (dibenzylidineacetone) palladium (2.55 g, 4.41 mmol) and tricyclohexylphosphine (2.4 g, 8.9 mmol) were added under reflux and heated and stirred for 11 hours. After completion of the reaction, the temperature was lowered to room temperature and then filtered. The filtrate was poured into water, extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. After distillation under reduced pressure, the residue was recrystallized from ethanol to obtain Compound 1-C (53 g, yield: 81%).

MS [M + H] &lt; ⁺ &gt; = 436

4) Synthesis of the following compound 2-1

[Compound 1-C] [Compound 2-1]

The compound 1-C (24.6 g, 56.6 mmol) and 1,4-dibromonaphthalene (7.7 g, 26.9 mmol) were completely dissolved in 160 ml of tetrahydrofuran, followed by addition of 2M aqueous potassium carbonate solution (80 ml) Tetraquistriphenylphosphinopalladium (600 mg, 0.51 mmol) was added thereto, followed by heating and stirring for 4 hours. After the temperature was lowered to room temperature and the reaction was terminated, the potassium carbonate solution was removed and the white solid was suspended. The filtered white solid was washed once with tetrahydrofuran and ethanol once to give the above compound 2-1 (18.0 g, yield 92%).

MS [M + H] &lt; ⁺ &gt; = 743

< Manufacturing example  2> Preparation of Compound 2-2

1) Synthesis of the following compound 2-A

[Compound 2-A]

Chloro-4-phenyl-6-biphenyl-1,3,5 triazine (45.5 g, 0.13 mol) and 4-chlorophenylboronic acid (18.43 g, 0.15 mol) After completely dissolved in 200 ml of hydrofuran, 2M aqueous potassium carbonate solution (100 ml) was added, tetrakis- (triphenylphosphine) palladium (3.1 g, 2.6 mmol) was added and the mixture was heated and stirred for 8 hours. The temperature was lowered to room temperature, the water layer was removed, dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and subjected to column chromatography with tetrahydrofuran: hexane = 1: 6 to prepare Compound 1-A (46 g, yield: 82%).

MS [M + H] &lt; ⁺ &gt; = 420

2) Synthesis of the following compound 2-B

[Compound 2-A] [Compound 2-B]

The compound 2-A (42.5 g, 101.2 mmol), bis (pinacolato) diboron (30.8 g, 121.5 mmol) and potassium acetate (30.8 g, 121.5 mmol) were mixed in a nitrogen atmosphere and added to 300 ml of dioxane And heated with stirring. Bis (dibenzylidineacetone) palladium (1.2 g, 2.02 mmol) and tricyclohexylphosphine (1.13 g, 4.04 mmol) were added under reflux and heated and stirred for 14 hours. After completion of the reaction, 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, the compound 2-B (47 g, 91%) was prepared by recrystallization from ethanol.

MS [M + H] &lt; ⁺ &gt; = 512

3) Synthesis of the following compound 2-C

[Compound 2-B] [Compound 2-C]

After completely dissolving the compound 2-B (43.82 g, 257.1 mmol) and 1,4-dibromonaphthalene (24.5 g, 85.67 mmol) in tetrahydrofuran (180 ml), 2M aqueous potassium carbonate solution (90 ml) Tetraquistriphenylphosphinopalladium (1.9 g, 1.71 mmol) was added thereto, followed by heating and stirring for 6 hours. After the temperature was lowered to room temperature and the reaction was terminated, the potassium carbonate solution was removed and the white solid was suspended. The filtered solid was washed once with tetrahydrofuran and once with ethanol to give the compound 2-C (45 g, yield 89%).

MS [M + H] &lt; ⁺ &gt; = 591

4) Synthesis of the following compound 2-2

[Compound 2-C] [Compound 1-C] [Compound 2-2]

The compound 1-C (15.85 g, 36.4 mmol) was completely dissolved in 120 ml of tetrahydrofuran, followed by the addition of 2M aqueous potassium carbonate solution (60 ml), and tetrakis triphenyl -Phosphino palladium (0.8 g, 0.73 mmol) were added, and the mixture was heated and stirred for 5 hours. After the temperature was lowered to room temperature and the reaction was terminated, the potassium carbonate solution was removed and the white solid was suspended. The filtered solid was washed once with tetrahydrofuran and once with ethanol to give the above compound 2-2 (25 g, yield 84%).

MS [M + H] &lt; ⁺ &gt; = 819

< Manufacturing example  3> Preparation of the following compounds 2-3

1) Synthesis of the following compound 2-E

[Compound 2-D] [Compound 2-E]

Compound 2-E was prepared in the same manner as Compound 2-C except for using 2-D instead of Compound 2-B.

MS [M + H] &lt; ⁺ &gt; = 667

2) Synthesis of Compound 2-3 below

[Compound 2-E] [Compound 1-C] [Compound 2-3]

Compound 2-3 was prepared in the same manner as Compound 2-2 except for using 2-E instead of Compound 2-C.

MS [M + H] &lt; ⁺ &gt; = 895

< Manufacturing example  4> Preparation of the following compound 2-4

1) Synthesis of the following compound 2-4

[Compound 2-B] [Compound 2-4]

Compound 2-4 was prepared in the same manner as Compound 2-1 except for using 2-B instead of Compound 1-C.

MS [M + H] &lt; ⁺ &gt; = 895

< Manufacturing example  5> Preparation of the following compound 2-5

1) Synthesis of the following compound 2-5

[Compound 2-E] [Compound 2-B] [Compound 2-5]

     Compound 2-5 was prepared in the same manner as Compound 2-2 except for using 2-E and 2-B instead of 2-C and 1-C.

MS [M + H] &lt; ⁺ &gt; = 895

< Manufacturing example  6> Preparation of the following compounds 2-6

1) Synthesis of the following compound 2-6

[Compound 2-D] [Compound 2-6]

Compound 2-6 was prepared in the same manner as Compound 2-1 except for using 2-D instead of Compound 1-C.

MS [M + H] &lt; ⁺ &gt; = 1047

< Manufacturing example  7> Preparation of the following compound 2-7

1) Synthesis of the following compound 2-F

[Compound 2-F]

The compound 4-chloro-2,6-diphenylpyrimidine (37.3 g, 0.14 mol) and 4-chlorophenylboronic acid (23.8 g, 0.15 mol) were completely dissolved in 150 ml of tetrahydrofuran in a nitrogen atmosphere, Potassium carbonate aqueous solution (80 ml) was added, and tetrakis- (triphenylphosphine) palladium (3.2 g, 2.7 mmol) was added thereto, followed by heating and stirring for 5 hours. The temperature was lowered to room temperature, and the water layer was removed. The organic layer was dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and subjected to column chromatography with tetrahydrofuran: hexane = 1: 6 to prepare the above compound 2-F (34 g, yield 71%).

MS [M + H] &lt; ⁺ &gt; = 343

2) Synthesis of the following compound 2-G

[Compound 2-F] [Compound 2-G]

The compound 2-F (34.9 g, 98.9 mmol), bis (pinacolato) diboron (27.6 g, 108 mmol) and potassium acetate (29.1 g, 296 mmol) were mixed in a nitrogen atmosphere and added to 100 ml of dioxane. Respectively. Bis (dibenzylidineacetone) palladium (1.7 g, 2.94 mmol) and tricyclohexylphosphine (1.6 g, 5.9 mmol) were added under reflux and heated and stirred for 10 hours. After completion of the reaction, the temperature was lowered to room temperature and then filtered. The filtrate was poured into water, extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. After distillation under reduced pressure, the residue was recrystallized from ethanol to obtain the above compound 2-G (35 g, yield: 81%).

MS [M + H] &lt; ⁺ &gt; = 435

3) Synthesis of the following compound 2-7

[Compound 2-G] [Compound 2-7]

Compound 2-7 was prepared in the same manner as Compound 2-1 except for using 2-G instead of Compound 1-C.

MS [M + H] &lt; ⁺ &gt; = 741

< Manufacturing example  8> Preparation of Compound 2-17

1) Synthesis of the following compound 2-17

[Compound 2-H] [Compound 2-17]

Compound 2-17 was prepared in the same manner as Compound 2-1 except for using 2-H instead of Compound 1-C.

MS [M + H] &lt; ⁺ &gt; = 741

< Manufacturing example  9> Preparation of Compound 2-23

1) Synthesis of the following compound 2-23

[Compound 2-I] [Compound 2-23]

Compound 2-23 was prepared in the same manner as Compound 2-1 except for using 2-I instead of Compound 1-C.

MS [M + H] &lt; ⁺ &gt; = 739

< Manufacturing example  10> Preparation of Compound 3-1

1) Preparation of compound 3-A

[Compound 1-A] [Compound 3-A]

The compound 1-A (30.0 g, 0.11 mol) and 3-chlorophenylboronic acid (19.2 g, 0.12 mol) were completely dissolved in 200 ml of tetrahydrofuran in a nitrogen atmosphere, and 2M aqueous potassium carbonate solution (100 ml) , And tetrakis- (triphenylphosphine) palladium (2.5 g, 2.2 mmol) were added thereto, followed by heating and stirring for 6 hours. The temperature was lowered to room temperature, the water layer was removed, dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and subjected to column chromatography with tetrahydrofuran: hexane = 1: 6 to prepare the above compound 3-A (31 g, yield: 82%).

MS [M + H] &lt; ⁺ &gt; = 344

2) Synthesis of the following compound 3-B

[Compound 3-A] [Compound 3-B]

(12.9 g, 50.6 mmol) and potassium acetate (12.3 g, 1236 mmol) were added to 100 ml of dioxane in a nitrogen atmosphere, and the mixture was stirred . Bis (dibenzylidineacetone) palladium (727 mg, 1.26 mmol) and tricyclohexylphosphine (709 mg, 2.52 mmol) were added under reflux and heated and stirred for 10 hours. After completion of the reaction, 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, the compound 3-B (17 g, 94%) was prepared by recrystallization from ethanol.

MS [M + H] &lt; ⁺ &gt; = 436

3) Synthesis of the following compound 3-1

[Compound 3-B] [Compound 3-1]

After dissolving the compound 3-B (17.3 g, 39.7 mmol) and 1,4-dibromonaphthalene (5.4 g, 18.9 mmol) in 60 ml of tetrahydrofuran, 30 ml of a 2M potassium carbonate aqueous solution was added, Phosphino palladium (436 mg, 0.37 mmol) was added and the mixture was heated with stirring for 2 hours. After the temperature was lowered to room temperature and the reaction was terminated, the potassium carbonate solution was removed and the white solid was suspended. The filtered white solid was washed once with tetrahydrofuran and ethanol, respectively, to obtain the above compound 3-1 (12.2 g, yield: 87%).

MS [M + H] &lt; ⁺ &gt; = 743

< Manufacturing example  11> Preparation of Compound 3-2

1) Synthesis of the following compound 3-D

[Compound 3-C] [Compound 3-D]

Compound 3-D was prepared in the same manner as Compound 2-C except for using Compound 3-C instead of Compound 2-B.

MS [M + H] &lt; ⁺ &gt; = 591

2) Synthesis of the following compound 3-2

[Compound 3-D] [Compound 3-B] [Compound 3-2]

The compound 3-B (15.85 g, 36.4 mmol) was completely dissolved in 120 ml of tetrahydrofuran, followed by addition of 2M aqueous potassium carbonate solution (60 ml), and tetrakis triphenyl -Phosphino palladium (0.8 g, 0.73 mmol) were added, and the mixture was heated and stirred for 5 hours. After the temperature was lowered to room temperature and the reaction was terminated, the potassium carbonate solution was removed and the white solid was suspended. The filtered solid was washed once with tetrahydrofuran and once with ethanol to give Compound 3-2 (25 g, yield 84%).

MS [M + H] &lt; ⁺ &gt; = 819

< Manufacturing example  12> Preparation of compound 4-1

1) Synthesis of the following compound 4-A

[Compound 1-A] [Compound 4-A]

A was prepared in the same manner as the compound 1-B except that 3-chlorophenylboronic acid (19.2 g, 0.12 mol) was used instead of 4-chlorophenylboronic acid. .

MS [M + H] &lt; ⁺ &gt; = 344

2) Synthesis of the following compound 4-B

[Compound 4-A] [Compound 4-B]

Compound 4-B was prepared in the same manner as Compound 2-B except for using Compound 4-A instead of Compound 2-A.

MS [M + H] &lt; ⁺ &gt; = 436

3) Synthesis of the following compound 4-1

[Compound 4-B] [Compound 4-1]

Compound 4-1 was prepared in the same manner as Compound 2-1 except that Compound 4-B was used instead of Compound 1-C.

MS [M + H] &lt; ⁺ &gt; = 743

< Manufacturing example  13> Preparation of Compound 5-1

1) Synthesis of the following compound 5-A

[Compound 3-B] [Compound 5-A]

Compound 5-A was prepared in the same manner as Compound 2-C except for using Compound 3-B instead of Compound 2-B

MS [M + H] &lt; ⁺ &gt; = 515

2) Synthesis of the following compound 5-1

[Compound 5-A] [Compound 4-B] [Compound 5-1]

Compound 5-1 was prepared in the same manner as Compound 3-2 except for using Compound 5-A, 4-B instead of Compound 3-D, 3-B.

MS [M + H] &lt; ⁺ &gt; = 743

< Manufacturing example  14> Preparation of Compound 6-1

1) Synthesis of the following compound 6-A

[Compound 4-B] [Compound 6-A]

Compound 6-A was prepared in the same manner as Compound 2-C except for using Compound 4-B instead of Compound 2-B

MS [M + H] &lt; ⁺ &gt; = 515

2) Synthesis of the following compound 6-1

[Compound 6-A] [Compound 1-C] [Compound 6-1]

Compound 6-1 was prepared in the same manner as Compound 3-2 except for using Compound 6-A, 1-C instead of Compound 3-D, 3-B.

MS [M + H] &lt; ⁺ &gt; = 743

< Manufacturing example  15> Preparation of Compound 7-1

1) Synthesis of the following compound 7-1

[Compound 5-A] [Compound 1-C] [Compound 7-1]

Compound 7-1 was prepared in the same manner as Compound 3-2 except for using Compound 5-A, 1-C instead of Compound 3-D, 3-B.

MS [M + H] &lt; ⁺ &gt; = 743

< Experimental Example  1>

The glass substrate coated with ITO (indium tin oxide) thin film with a thickness of 1,000 Å was immersed in distilled water containing detergent and washed with ultrasonic waves. In this case, Fischer Co. was used as a detergent, and distilled water filtered by a filter of Millipore Co. was used as distilled water. The ITO was washed for 30 minutes and then washed twice with distilled water and ultrasonically cleaned for 10 minutes. After the distilled water was washed, it was ultrasonically washed with a solvent of isopropyl alcohol, acetone, and methanol, dried, and then transported to a plasma cleaner. Further, the substrate was cleaned using oxygen plasma for 5 minutes, and then the substrate was transported by a vacuum evaporator.

On this ITO transparent electrode, hexanitrile hexaazatriphenylene (HAT) of the following chemical formula was thermally vacuum deposited to a thickness of 500 Å to form a hole injection layer.

[LINE]

(4,4'-bis [N- (1-naphthyl) -N-phenylamino] biphenyl (NPB) (400 angstroms) as a hole transporting material was vacuum deposited on the hole injection layer to form a hole transport layer Respectively.

[NPB]

Subsequently, the following BH and BD were vacuum deposited on the hole transport layer at a weight ratio of 25: 1 at a thickness of 300 ANGSTROM to form a light emitting layer.

[BH]

[BD]

[LiQ]

The compound 2-1 prepared in Preparation Example 1 and the compound LiQ (Lithium Quinolate) were vacuum deposited on the light emitting layer at a weight ratio of 1: 1 to form an electron injection and transport layer having a thickness of 300 Å. Lithium fluoride (LiF) and aluminum were deposited to a thickness of 2000 Å on the electron injecting and transporting layer sequentially to form a cathode.

Was maintained at the deposition rate was 0.4 ~ 0.7Å / sec for organic material in the above process, the lithium fluoride of the cathode was 0.3Å / sec, aluminum is deposited at a rate of 2Å / sec, the degree of vacuum upon deposition ⅹ10 2 ^-7 To 5 x 10 &lt; ^-6 &gt; torr, thereby fabricating an organic light emitting device.

 <Experimental Example 2>

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that Compound 2-2 was used in place of Compound 2-1 in Experimental Example 1.

 <Experimental Example 3>

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that Compound 2-3 was used in place of Compound 2-1 in Experimental Example 1.

<Experimental Example 4>

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that Compound 2-4 was used instead of Compound 2-1 in Experimental Example 1.

<Experimental Example 5>

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that Compound 2-5 was used in place of Compound 2-1 in Experimental Example 1.

<Experimental Example 6>

An organic light emitting device was prepared in the same manner as in Experimental Example 1, except that Compound 2-6 was used in place of Compound 2-1 in Experimental Example 1.

<Experimental Example 7>

An organic light emitting device was prepared in the same manner as in Experimental Example 1, except that Compound 2-7 was used instead of Compound 2-1 in Experimental Example 1.

<Experimental Example 8>

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that Compound 2-17 was used instead of Compound 2-1 in Experimental Example 1.

<Experimental Example 9>

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that Compound 2-23 was used in place of Compound 2-1 in Experimental Example 1.

<Experimental Example 10>

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that Compound 3-1 was used instead of Compound 2-1 in Experimental Example 1.

&Lt; Experimental Example 11 &

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that Compound 4-1 was used instead of Compound 2-1 in Experimental Example 1.

<Experimental Example 12>

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that Compound 5-1 was used instead of Compound 2-1 in Experimental Example 1.

<Experimental Example 13>

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that Compound 6-1 was used instead of Compound 2-1 in Experimental Example 1.

<Experimental Example 14>

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that Compound 7-1 was used instead of Compound 2-1 in Experimental Example 1.

&Lt; Comparative Example 1 &

An organic light emitting device was prepared in the same manner as in Experimental Example 1, except that the compound of ET1 was used in place of the compound 2-1 in Experimental Example 1.

[ET1]

&Lt; Comparative Example 2 &

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that the compound of ET2 was used in place of the compound 1-1 in Experimental Example 1.

[ET2]

&Lt; Comparative Example 3 &

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that the following compound ET3 was used in place of Compound 1-1 in Experimental Example 1.

[ET3]

&Lt; Comparative Example 4 &

An organic light emitting device was fabricated in the same manner as in Experimental Example 1, except that the following compound was used in place of Compound 1-1 in Test Example 1.

[ET4]

compound Voltage
(V @ 10 mA / cm ² ) efficiency
(cd / A @ 10mA / cm 2) Color coordinates
(x, y) Experimental Example 1 Compound 2-1 3.75 5.11 (0.138, 0.127) Experimental Example 2 Compound 2-2 3.88 4.95 (0.139, 0.122) Experimental Example 3 Compound 2-3 3.86 5.04 (0.138, 0.126) Experimental Example 4 Compound 2-4 3.85 4.72 (0.138, 0.127) Experimental Example 5 Compound 2-5 3.89 4.65 (0.137, 0.129) Experimental Example 6 Compound 2-6 3.88 4.61 (0.136, 0.129) Experimental Example 7 Compound 2-7 3.83 4.63 (0.137, 0.128) Experimental Example 8 Compound 2-17 3.89 4.62 (0.138, 0.129) Experimental Example 9 Compound 2-23 3.87 4.64 (0.138, 0.128) Experimental Example 10 Compound 3-1 3.74 5.08 (0.138, 0.129) Experimental Example 11 Compound 3-2 3.96 4.71 (0.137, 0.128) Experimental Example 12 Compound 4-1 3.82 4.72 (0.137, 0.129) Experimental Example 13 Compound 5-1 3.83 4.76 (0.137, 0.129) Experimental Example 14 Compound 6-1 3.86 4.74 (0.136, 0.129) Experimental Example 15 Compound 7-1 3.84 4.73 (0.137, 0.130) Comparative Example 1 ET1 4.28 3.68 (0.132, 0.138) Comparative Example 2 ET2 4.35 3.74 (0.133, 0.127) Comparative Example 3 ET3 4.05 4.46 (0.136, 0.130) Comparative Example 4 ET4 4.03 4.42 (0.136, 0.130)

As shown in the above Table 1, the comparison between Experimental Example 1 and Comparative Example 1 shows that when triazine is bound to both of the 1,4-naphthalene core and the core, the electron transporting and injecting ability is superior .

As shown in Table 1, when Experimental Example 1 and Comparative Examples 1 and 2 were compared, it was found that when triazine was connected to 1,4-naphthalene by connecting a phenylene group, the electron transporting and injecting ability was superior to the direct bonding Can be confirmed.

As shown in Table 1, when the experimental examples 10, 12, 13, 14 and 15 and the comparative examples 3 to 4 are compared, it can be seen that the core of the heterocyclic compound according to one embodiment of the present invention is 1,4-naphthyl group , It can be confirmed that the electron transporting and injecting ability is superior to the 1,5-naphthyl group or the 2,6-naphthyl group. Also, when the substituents are bonded symmetrically or asymmetrically in the direction of ortho, meta and para, they exhibit low voltage and high efficiency characteristics.

As shown in Table 1, the results of Experimental Examples 3, 4, 5, 6, 7, 8, and 9 show that pyrimidine and pyridine substituents are bonded to 1,4-naphthalene linked symmetrically or asymmetrically with phenylene It can be confirmed that the electron transporting and injecting ability is excellent.

As shown in the results of Table 1, it was confirmed that the compounds of the present invention are excellent in electron transporting and injecting ability and applicable to organic light emitting devices.

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

Claims (15)

A heterocyclic compound represented by the following formula (1):
[Chemical Formula 1]

In formula (1)
X1 to X3 are the same or different from each other and are each CH or N,
At least one of X1 to X3 is N,
X4 to X6 are the same or different and each is CH or N,
At least one of X4 to X6 is N,
Ar 1 to Ar 4 are the same or different and are each independently a substituted or unsubstituted aryl group. The method according to claim 1,
The heterocyclic compound represented by the formula (1) is represented by any one of the following formulas (2) to (7)
(2)

(3)

[Chemical Formula 4]

[Chemical Formula 5]

[Chemical Formula 6]

(7)

In formulas (2) to (7)
Ar1 to Ar4 and X1 to X6 are the same as defined in claim 1. The method according to claim 1,
Ar 1 to Ar 4 are the same or different and each independently represents a substituted or unsubstituted phenyl group; Or a substituted or unsubstituted biphenyl group. The method according to claim 1,
Wherein the heterocyclic compound represented by the formula (1) is any one of the following formulas (2-1) to (2-32).

The method according to claim 1,
The heterocyclic compound represented by the formula (1) is any one of the following formulas (3-1) to (3-32).

The method according to claim 1,
Wherein the heterocyclic compound represented by the formula (1) is any one of the following formulas (4-1) to (4-32).

The method according to claim 1,
The heterocyclic compound represented by the formula (1) is any one of the following formulas (5-1) to (5-50).

The method according to claim 1,
The heterocyclic compound represented by the formula (1) is any one of the following formulas (6-1) to (6-50).

The method according to claim 1,
Wherein the heterocyclic compound represented by the formula (1) is any one of the following formulas (7-1) to (7-50).

A first electrode; A second electrode facing the first electrode; And at least one organic layer including a light emitting layer provided between the first electrode and the second electrode,
Wherein at least one of the organic material layers comprises the heterocyclic compound according to any one of claims 1 to 9. The method of claim 10,
Wherein the organic material layer includes an electron transporting layer, an electron injecting layer, or a layer simultaneously performing electron transport and electron injection,
Wherein the electron transporting layer, the electron injecting layer, or the layer that simultaneously transports electrons and injects electrons comprises the heterocyclic compound. The method of claim 10,
Wherein the light emitting layer comprises the heterocyclic compound. The method of claim 10,
Wherein the organic material layer includes a hole blocking layer,
Wherein the hole blocking layer comprises the heterocyclic compound. The method of claim 10,
Wherein the organic material layer includes a hole transporting layer, a hole injecting layer, or a layer simultaneously injecting holes and transporting holes,
Wherein the hole transport layer, the hole injection layer, or the layer that simultaneously injects holes and transports the hole transport layer includes the heterocyclic compound. The method of claim 10,
Wherein the organic material layer is a hole injection layer, a hole transport layer. An electron transport layer, an electron injection layer, an electron blocking layer, and a hole blocking layer.

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