KR20110061792A - Compound containing dibenzocarbazole and organic electronic element using the same, terminal thereof - Google Patents

Abstract

PURPOSE: A compound containing dibenzocarbazole is provided to enable use as a hole injection layer or hole transport layer in an organic electric device, and to ensure efficiency increase, driving voltage lowering, lifetime increase and stability enhancement when applied to the organic electric device. CONSTITUTION: A compound has structure represented by chemical formula. The organic electric device comprises an organic material layer including the compound. The compound forms the organic layer by a solution process. The organic electric device is an organic electroluminescence device including a first electrode, an organic layer, and a second electrode. The organic material layer is one of a hole injection layer, hole transport layer, electroluminescent layer, electron transport layer and electron injection layer.

Description

Compound Containing Dibenzocarbazole And Organic Electronic Element Using The Same, Terminal Thereof}

The present invention relates to a compound having a dibenzocarbazole, an organic electric device using the same, and a terminal thereof.

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 electric device using an organic light emitting phenomenon generally has a structure including an anode, an anode, and an organic material layer therebetween. In this case, the organic material layer is often formed of a multi-layered structure composed of different materials in order to increase the efficiency and stability of the organic electric device, for example, it may be made of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer and an electron injection layer.

Materials used as the organic material layer in the organic electric element may be classified into light emitting materials and charge transport materials, such as hole injection materials, hole transport materials, electron transport materials, electron injection materials, and the like, depending on their functions. The light emitting material may be classified into a polymer type and a low molecular type according to molecular weight, and may be classified into a fluorescent material derived from a singlet excited state of electrons and a phosphorescent material derived from a triplet excited state of electrons according to a light emitting mechanism. Can be classified. In addition, the light emitting material may be classified into blue, green, and red light emitting materials and yellow and orange light emitting materials required to achieve a better natural color according to the light emitting color.

On the other hand, when only one material is used as a light emitting material, there arises a problem that the maximum light emission wavelength shifts to a long wavelength due to intermolecular interaction, the color purity decreases, or the efficiency of the device decreases due to the light emission attenuating effect. A host / dopant system may be used as the light emitting material in order to increase the light emitting efficiency through the light emitting layer. The principle is that when a small amount of dopant having an energy band gap smaller than that of a host forming the light emitting layer is mixed in the light emitting layer, excitons generated in the light emitting layer are transported to the dopant, thereby producing high-efficiency light. At this time, since the wavelength of the host is shifted to the wavelength band of the dopant, the desired wavelength light can be obtained depending on the type of the dopant used.

In order to fully exhibit the excellent characteristics of the above-described organic electroluminescent device, a material forming the organic material layer in the device, such as a hole injection material, a hole transport material, a light emitting material, an electron transport material, an electron injection material, etc., is supported by a stable and efficient material. Although this should be preceded, the development of a stable and efficient organic material layer for an organic electric element has not yet been made sufficiently, and therefore, the development of new materials is continuously required.

Embodiment of the present invention for solving the problems of the above-described background, a compound having a dibenzo carbazole having a novel structure has been found, and the luminous efficiency and stability of the device when applying this compound to an organic electric device And it has been found that the life can be greatly improved.

Accordingly, an object of the present invention is to provide a compound having a novel dibenzocarbazole, an organic electric device using the same, and a terminal thereof.

In one aspect, the present invention provides a compound of the formula:

The present invention can be used as a compound having a dibenzo carbazole as a hole injection, hole transport, electron injection, electron transport, light emitting material and / or passivation (kepping) material, in particular can be used as a host or dopant alone.

In addition, the present invention can be used as a hole injection layer or a hole transport layer in the organic electronic device, it has been found that the effect of increasing the efficiency of the organic electronic device, including the driving voltage, increase in life and stability increase.

Accordingly, the present invention provides a compound having a dibenzocarbazole as a core, an organic electronic device using the same, and a terminal including the organic electronic device.

The present invention is a compound having a dibenzo carbazole is useful as a hole injection, hole transport, electron injection, electron transport, light emitting material and / or passivation (kepping) material, in particular as a host or dopant alone.

Hereinafter, some embodiments of the present invention will be described in detail through exemplary drawings. In adding reference numerals to the components of each drawing, it should be noted that the same reference numerals are assigned to the same components as much as possible even though they are shown in different drawings. In the following description of the present invention, a detailed description of known functions and configurations incorporated herein will be omitted when it may make the subject matter of the present invention rather unclear.

In addition, in describing the component of this invention, terms, such as 1st, 2nd, A, B, (a), (b), can be used. These terms are only for distinguishing the components from other components, and the nature, order or order of the components are not limited by the terms. If a component is described as being "connected", "coupled" or "connected" to another component, that component may be directly connected to or connected to that other component, but there may be another configuration between each component. It is to be understood that the elements may be "connected", "coupled" or "connected".

The present invention provides a compound of Formula 1 below.

In Formula 1, R1 to R14 are the same as or different from each other, and each independently a halogen group, a C ₁ to C ₆₀ alkyl group, a C ₁ to C ₆₀ alkoxy group, a C ₁ to C ₆₀ alkylamine group, C ₁ to C ₆₀ arylamine group, C ₁ -C ₆₀ alkyl thiophene group, C ₆ -C ₆₀ aryl thiophene group, C ₂ -C ₆₀ alkenyl group, C ₂ -C ₆₀ alkynyl group, C _3- for C ₆₀ cycloalkyl group, C ₆ ~ C ₆₀ aryl group, of a C ₆ ~ C ₆₀ substituted by deuterium aryl group, a C ₈ ~ arylalkenyl group, a substituted or unsubstituted silane group, a substituted or unsubstituted of C ₆₀ A C ₆ to C ₆₀ aryl group unsubstituted or substituted with one or more groups selected from the group consisting of a boron group, a substituted or unsubstituted germanium group, and a substituted or unsubstituted C ₅ to C ₆₀ heterocyclic group; Halogen, CN, NO ₂ , C ₁ to C ₆₀ alkyl group, C ₁ to C ₆₀ alkoxy group, C ₁ to C ₆₀ alkylamine group, C ₁ to C ₆₀ arylamine group, C ₁ to C ₆₀ the alkylthio group, C ₂ ~ C ₆₀ alkenyl group, C ₂ ~ C ₆₀ alkynyl group, C ₃ ~ C ₆₀ cycloalkyl group, C ₆ ~ C ₆₀ aryl group, a C ₆ ~ C ₆₀ substituted with a heavy hydrogen of the Substituted with one or more groups selected from the group consisting of an aryl group, a substituted or unsubstituted silane group, a substituted or unsubstituted boron group, a substituted or unsubstituted germanium group, and a substituted or unsubstituted C ₅ to C ₆₀ heterocyclic group Or an unsubstituted C ₅ ~ C ₆₀ heterocyclic group; Or a condensed ring group of a C ₆ to C ₆₀ aromatic ring and a C ₄ to C ₆₀ aliphatic ring, each independently a hydrogen atom, a halogen atom, a substituted or unsubstituted aliphatic hydrocarbon group, a substituted or unsubstituted aryl group , Any group selected from substituted and unsubstituted heteroaryl groups, and adjacent positions may be bonded to each other to form a ring.

(2) L represents a group selected from a substituted or unsubstituted arylene group, a substituted or unsubstituted hetero arylene group, and a divalent or trivalent substituted or unsubstituted aliphatic hydrocarbon.

In another aspect, the present invention provides a compound of Formula 2 below. The compound of formula 2 corresponds to the case where L is divalent in formula (1).

In Formula 2, R1 to R14, L is the same as that of Formula 1.

In another aspect, the present invention provides a compound of Formula 3 below. The compound of Formula 3 corresponds to the case where L is trivalent in Formula 1.

In Formula 2, R1 to R14, L is the same as that of Formula 1.

Specific examples of the compounds belonging to Formulas 1 to 3, which are compounds having dibenzocarbazole according to one embodiment of the present invention, may be compounds represented by the following Formulas 4 and 5, but the present invention is not limited thereto.

Various organic electric devices exist in which compounds having dibenzocarbazole described with reference to Chemical Formulas 1 to 5 are used as the organic material layer. Examples of the organic electroluminescent device in which the compounds having dibenzocarbazole described with reference to Chemical Formulas 1 to 5 may be used include, for example, an organic light emitting diode (OLED), an organic solar cell, an organic photoconductor (OPC) drum, and an organic transistor ( Organic TFTs).

As an example of the organic electroluminescent device to which the compounds having dibenzocarbazole described with reference to Chemical Formulas 1 to 5 may be applied, an organic light emitting diode (OLED) is described, but the present invention is not limited thereto. Compounds having the dibenzocarbazoles described above can be applied.

Another embodiment of the present invention is an organic electric device comprising a first electrode, a second electrode and an organic material layer disposed between the electrodes, wherein at least one of the organic material layer of the organic electric field comprising the compounds of Formula 1 to 5 Provided is a light emitting device.

1 to 6 show examples of the organic light emitting display device to which the compound of the present invention can be applied.

The organic light emitting device according to another embodiment of the present invention, a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer And a structure known in the art using conventional manufacturing methods and materials in the art, except that at least one layer of the organic material layer including the electron injection layer is formed to include the compounds of Formulas 1 to 5. It can be prepared as.

The structure of the organic light emitting display device according to another embodiment of the present invention is illustrated in FIGS. 1 to 6, but is not limited thereto. In this case, reference numeral 101 denotes a substrate, 102 an anode, 103 a hole injection layer (HIL), 104 a hole transport layer (HTL), 105 a light emitting layer (EML), 106 an electron injection layer (EIL), 107 an electron transport layer ( ETL), 108 represents a negative electrode. Although not shown, the organic light emitting diode may further include a hole blocking layer (HBL) for blocking the movement of holes, an electron blocking layer (EBL) for preventing the movement of electrons, and a protective layer. The protective layer may be formed to protect the organic material layer or the cathode at the uppermost layer.

In this case, the compound having the dibenzocarbazole described with reference to Formulas 1 to 5 may be included in one or more of an organic material layer including a hole injection layer, a hole transport layer, a light emitting layer and an electron transport layer. Specifically, the compound having a dibenzocarbazole described with reference to Formulas 1 to 5 instead of one or more of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer, a hole blocking layer, an electron blocking layer, a protective layer Or may be used together with them to form a layer. Of course, the organic layer may be used not only in one layer but also in two or more layers.

In particular, it can be used as a hole injection material, a hole transport material, an electron injection material, an electron transport material, a light emitting material and a passivation (kepping) material according to the compound having a dibenzo carbazole described with reference to Formulas 1 to 5, in particular It can be used as a light emitting material and a host or dopant.

In particular, it can be used as a hole injection material according to the compound having dibenzocarbazole described with reference to the formula (1) to (5).

For example, the organic light emitting device according to another embodiment of the present invention is a metal having a metal or conductivity on a substrate by using a physical vapor deposition (PVD) method such as sputtering or e-beam evaporation An oxide or an alloy thereof is deposited to form an anode, an organic material layer including a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, and an electron injection layer is formed thereon, and then a material that can be used as a cathode is deposited thereon. Can be prepared.

In addition to the above method, an organic electronic device may be fabricated by sequentially depositing a cathode material, an organic material layer, and an anode material on a substrate. The organic material layer may have a multilayer structure including a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer and an electron injection layer, but is not limited thereto and may have a single layer structure. In addition, the organic material layer may be formed using a variety of polymer materials by a solvent process such as a spin coating process, a dip coating process, a doctor blading process, a screen printing process, an inkjet printing process or a thermal transfer process, Layer.

The organic electroluminescent device according to another embodiment of the present invention may be used in a solution process such as spin coating or an ink jet process using the compound having dibenzocarbazole described above.

The substrate is a support of the organic light emitting device, and a silicon wafer, quartz or glass plate, metal plate, plastic film or sheet, or the like can be used.

An anode is positioned over the substrate. This anode injects holes into the hole injection layer located thereon. 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 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] (PEDT), polypyrrole and polyaniline.

The hole injection layer is located on the anode. The conditions required for the material of the hole injection layer are high hole injection efficiency from the anode, it should be able to transport the injected holes efficiently. This requires a small ionization potential, high transparency to visible light, and excellent hole stability.

As the hole injecting material, 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 hole injection materials include metal porphyrine, oligothiophene, arylamine-based organics, hexanitrile hexaazatriphenylene, quinacridone-based organics, perylene-based organics, Anthraquinone, polyaniline and polythiophene-based conductive polymers, but are not limited thereto.

The hole transport layer is positioned on the hole injection layer. The hole transport layer receives holes from the hole injection layer and transports the holes to the organic light emitting layer located thereon, and serves to prevent high hole mobility, hole stability, and electrons. In addition to these general requirements, when applied for vehicle body display, heat resistance to the device is required, and a material having a glass transition temperature (Tg) of 70 ° C. or higher is preferable. Materials satisfying these conditions include NPD (or NPB), spiro-arylamine compounds, perylene-arylamine compounds, azacycloheptatriene compounds, bis (diphenylvinylphenyl) anthracene, silicon germanium oxide Compound, a silicon-based arylamine compound, and the like.

The organic light emitting layer is positioned on the hole transport layer. The organic light emitting layer is a layer for emitting light by recombination of holes and electrons injected from the anode and the cathode, respectively, and is made of a material having high quantum efficiency. 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.

Substances or compounds that satisfy these conditions include Alq3 for green, Balq (8-hydroxyquinoline beryllium salt) for blue, DPVBi (4,4'-bis (2,2-diphenylethenyl) -1,1'- biphenyl) series, Spiro material, Spiro-DPVBi (Spiro-4,4'-bis (2,2-diphenylethenyl) -1,1'-biphenyl), LiPBO (2- (2-benzoxazoyl) -phenol lithium salt), bis (diphenylvinylphenylvinyl) benzene, aluminum-quinoline metal complex, metal complexes of imidazole, thiazole and oxazole, and the like, perylene, and BczVBi (3,3 ') to increase blue light emission efficiency. [(1,1'-biphenyl) -4,4'-diyldi-2,1-ethenediyl] bis (9-ethyl) -9H-carbazole; DSA (distrylamine) can be used by doping in small amounts. In the case of red, DCJTB ([2- (1,1-dimethylethyl) -6- [2- (2,3,6,7-tetrahydro-1,1,7,7-tetramethyl-1H, 5H Small amounts of doping such as -benzo (ij) quinolizin-9-yl) ethenyl] -4H-pyran-4-ylidene] -propanedinitrile) can be used. When the light emitting layer is formed using a process such as inkjet printing, roll coating, or spin coating, an organic light emitting layer is formed of a polymer of polyphenylene vinylene (PPV) or a polymer such as poly fluorene. Can be used for

The electron transport layer is positioned on the organic light emitting layer. The electron transport layer needs a material having high electron injection efficiency from the cathode disposed thereon and efficiently transporting the injected electrons. To this end, it must be made of a material having high electron affinity and electron transfer speed and excellent stability to electrons. Examples of the electron transport material that satisfies such conditions 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 injection layer is stacked on the electron transport layer. The electron injection layer is a metal complex compound such as Balq, Alq3, Be (bq) 2, Zn (BTZ) 2, Zn (phq) 2, PBD, spiro-PBD, TPBI, Tf-6P, aromatic compound with imidazole ring, It can be produced using a low molecular weight material containing boron compounds and the like. At this time, the electron injection layer may be formed in a thickness range of 100 ~ 300Å.

The cathode is positioned on the electron injection layer. This cathode serves to inject electrons. As the material used as the cathode, it is possible to use the material used for the anode, and a metal having a low work function is more preferable for efficient electron injection. In particular, a suitable metal such as tin, magnesium, indium, calcium, sodium, lithium, aluminum, silver, or a suitable alloy thereof can be used. In addition, an electrode having a two-layer structure such as lithium fluoride and aluminum, lithium oxide and aluminum, strontium oxide and aluminum having a thickness of 100 μm or less may also be used.

As described above, it may be used as a hole injection material, a hole transport material, an electron injection material, an electron transport material, a light emitting material and a passivation (kepping) material according to the compound having a dibenzo carbazole described with reference to Formulas 1 to 5, in particular It can be used alone as a light emitting material and as a host or dopant.

In particular, it can be used as a hole injection material according to the compound having dibenzocarbazole described with reference to the formula (1) to (5).

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 according to the material used.

Meanwhile, the present invention includes a display device including the organic electric element described above, and a terminal including a control unit for driving the display device. This terminal means a current or future wired or wireless communication terminal. The terminal according to the present invention described above may be a mobile communication terminal such as a mobile phone, and includes all terminals such as a PDA, an electronic dictionary, a PMP, a remote controller, a navigation device, a game machine, various TVs, various computers, and the like.

Example

Hereinafter, the present invention will be described in more detail with reference to Preparation Examples and Experimental Examples. However, the following Preparation Examples and Experimental Examples are for illustrating the present invention, and the scope of the present invention is not limited thereto.

Manufacturing example

Hereinafter, the preparation or synthesis examples of the compounds having dibenzocarbazole belonging to formulas (4) and (5) will be described. However, since a large number of compounds having dibenzocarbazole belonging to Formulas 4 and 5, one or two of the compounds having dibenzocarbazole belonging to Formulas 4 and 5 will be exemplarily described. Those skilled in the art, that is, those skilled in the art can prepare a compound having dibenzocarbazole belonging to the present invention, which is not illustrated by the preparation examples described below.

Synthetic

In the above synthesis, when A is Phenanthrene and Ar is H, Phenyl, or Methyl, intermediate 3 and intermediate 7 can be easily synthesized by those skilled in the art, and thus, detailed descriptions thereof will be omitted. (To determine more specific synthesis method, tetrahedron Vol. 30 2983, (1974)).

1. Synthesis of Compound A-28

Referring to Scheme 2, starting material 1 and N- (4'-bromobiphenyl-4-yl) -N- (9,9-dimethyl-9H-fluoren-2-yl) -9,9-dimethyl-9H-fluoren -2-amine, Pd ₂ (dba) ₃ , Triphenylphosphine and Sodium tert-butoxide are added to toluene solvent and stirred under reflux for 24 hours at 130 ° C.

After completion of the reaction, the mixture was extracted with MC and water, dried over MgSO ₄ , concentrated and the resulting compound was separated using column chromatography to obtain the desired compound A-29 in a yield of 67%.

2. Synthesis of Compound B-3

Referring to Scheme 2, toluene starting materials 1 and 4'-bromo-N3, N3, N5, N5-tetrap-tolylbiphenyl-3,5-diamine, Pd ₂ (dba) ₃ , Triphenyl-phosphine, Sodium tert-butoxide Put in a solvent and stirred under reflux for 24 hours at 130 degrees.

After completion of the reaction, the mixture was extracted with MC, water, dried over MgSO ₄ , concentrated and the resulting compound was separated by column chromatography to obtain the desired compound B-3 in 61% yield.

Manufacturing Evaluation of Organic Field Devices

Various compounds obtained through synthesis were used as light emitting host materials or hole transporting layers of the light emitting layer, respectively, to fabricate an organic light emitting device according to a conventional method. First, a copper phthalocyanine (hereinafter abbreviated as CuPc) film was vacuum-deposited on the ITO layer (anode) formed on the glass substrate to form a thickness of 10 nm.

Subsequently, the material developed as a major transport compound was vacuum deposited to a thickness of 30 nm to form a hole transport layer. After the hole transport layer was formed, the developed material was measured by measuring the hole transport layer with a 45 nm-thick BD-052X (Idemitus Co., Ltd.) 7% doped light emitting layer (where BD-052X is a blue fluorescent dopant) 9,10-di (naphthalene-2-anthracene (AND)) was used as the light emitting host material.

(1,1'-bisphenyl) -4-oleito) bis (2-methyl-8-quinolineoleito) aluminum (hereinafter abbreviated as BAlq) was vacuum deposited to a hole blocking layer to a thickness of 10 nm, Subsequently, tris (8-quinolinol) aluminum (hereinafter abbreviated as Alq ₃ ) was formed into an electron transport layer to a thickness of 40 nm. Thereafter, LiF, an alkali metal halide, was deposited to a thickness of 0.2 nm, and then Al was deposited to a thickness of 150 nm to use an Al / LiF as a cathode to prepare an organic light emitting device.

Comparative Experimental Example

When the compounds of Chemical Formulas 1 to 5 described above were measured by the hole transport layer, the compound represented by the following Chemical Formula 6 (hereinafter abbreviated as NPB) was used as the hole transport material in place of the compound of the present invention for comparison. An organic electroluminescent device having a structure was fabricated.

Hole transport
material Voltage
(V) Current density
(mA / cm ² ) Luminous efficiency
(cd / A) Chromaticity coordinates
(x, y) Example 1 Compound A-13 6.7 12.98 8.1 (0.15, 0.13) Example 2 Compound a -27 6.3 12.78 8.4 (0.15, 0.14) Example 3 Compound a -28 6.3 13.02 8.3 (0.15, 0.13) Example 4 Compound b-3 6.6 13.21 8.1 (0.15, 0.14) Comparative Example 1 NPB 7.2 13.35 7.5 (0.15, 0.15)

As can be seen from the results of Table 1, it can be seen that the organic electroluminescent device using the organic light emitting device material of the present invention exhibits the effect of increasing the efficiency of the organic electronic device, lowering the driving voltage, increasing the lifetime, and increasing the stability.

It is apparent that the compounds of the present invention can achieve the same effect even when other organic material layers of the organic light emitting device are used, for example, a hole transport layer, an electron injection layer, an electron transport layer, a light emitting layer, and a hole injection layer.

While the present invention has been described in connection with what is presently considered to be practical exemplary embodiments thereof, it is to be understood that the invention is not limited to the disclosed embodiments, but, on the contrary, It will be understood that the invention may be practiced. Therefore, the embodiments described above are to be understood as illustrative and not restrictive in all aspects. In addition, the scope of the present invention is shown by the claims below, rather than the above detailed description. Also, it is to be construed that all changes or modifications derived from the meaning and scope of the claims and their equivalent concepts are included in the scope of the present invention.

1 to 6 show examples of the organic light emitting display device to which the compound of the present invention can be applied.

Claims (12)

Compound represented by the following formula.

In the formula, R1 to R14 are the same as or different from each other, and each independently a halogen group, a C ₁ to C ₆₀ alkyl group, a C ₁ to C ₆₀ alkoxy group, a C ₁ to C ₆₀ alkylamine group, C ₁ to C ₆₀ arylamine group, C ₁ to C ₆₀ alkyl thiophene group, C ₆ to C ₆₀ aryl thiophene group, C ₂ to C ₆₀ alkenyl group, C ₂ to C ₆₀ alkynyl group, C ₃ to C ₆₀ cycloalkyl group, C ₆ ~ C ₆₀ aryl group, of a C ₆ ~ C ₆₀ substituted by deuterium aryl group, a C ₈ ~ C ₆₀ arylalkenyl group, a substituted or unsubstituted silane group, a substituted or unsubstituted ring of A C ₆ -C ₆₀ aryl group unsubstituted or substituted with one or more groups selected from the group consisting of a boron group, a substituted or unsubstituted germanium group, and a substituted or unsubstituted C ₅ -C ₆₀ heterocyclic group; Halogen, CN, NO ₂ , C ₁ to C ₆₀ alkyl group, C ₁ to C ₆₀ alkoxy group, C ₁ to C ₆₀ alkylamine group, C ₁ to C ₆₀ arylamine group, C ₁ to C ₆₀ the alkylthio group, C ₂ ~ C ₆₀ alkenyl group, C ₂ ~ C ₆₀ alkynyl group, C ₃ ~ C ₆₀ cycloalkyl group, C ₆ ~ C ₆₀ aryl group, a C ₆ ~ C ₆₀ substituted with a heavy hydrogen of the Substituted with one or more groups selected from the group consisting of an aryl group, a substituted or unsubstituted silane group, a substituted or unsubstituted boron group, a substituted or unsubstituted germanium group, and a substituted or unsubstituted C ₅ to C ₆₀ heterocyclic group Or an unsubstituted C ₅ ~ C ₆₀ heterocyclic group; Or a condensed ring group of a C ₆ to C ₆₀ aromatic ring and a C ₄ to C ₆₀ aliphatic ring, each independently a hydrogen atom, a halogen atom, a substituted or unsubstituted aliphatic hydrocarbon group, a substituted or unsubstituted aryl group , A substituted and unsubstituted hetero aryl group. (2) L represents a group selected from a substituted or unsubstituted arylene group, a substituted or unsubstituted hetero arylene group, and a divalent or trivalent substituted or unsubstituted aliphatic hydrocarbon. Compound represented by the following formula.

In the formula, R1 to R14 are the same as or different from each other, and each independently a halogen group, a C ₁ to C ₆₀ alkyl group, a C ₁ to C ₆₀ alkoxy group, a C ₁ to C ₆₀ alkylamine group, C ₁ to C ₆₀ arylamine group, C ₁ to C ₆₀ alkyl thiophene group, C ₆ to C ₆₀ aryl thiophene group, C ₂ to C ₆₀ alkenyl group, C ₂ to C ₆₀ alkynyl group, C ₃ to C ₆₀ cycloalkyl group, C ₆ ~ C ₆₀ aryl group, of a C ₆ ~ C ₆₀ substituted by deuterium aryl group, a C ₈ ~ C ₆₀ arylalkenyl group, a substituted or unsubstituted silane group, a substituted or unsubstituted ring of A C ₆ -C ₆₀ aryl group unsubstituted or substituted with one or more groups selected from the group consisting of a boron group, a substituted or unsubstituted germanium group, and a substituted or unsubstituted C ₅ -C ₆₀ heterocyclic group; Halogen, CN, NO ₂ , C ₁ to C ₆₀ alkyl group, C ₁ to C ₆₀ alkoxy group, C ₁ to C ₆₀ alkylamine group, C ₁ to C ₆₀ arylamine group, C ₁ to C ₆₀ the alkylthio group, C ₂ ~ C ₆₀ alkenyl group, C ₂ ~ C ₆₀ alkynyl group, C ₃ ~ C ₆₀ cycloalkyl group, C ₆ ~ C ₆₀ aryl group, a C ₆ ~ C ₆₀ substituted with a heavy hydrogen of the Substituted with one or more groups selected from the group consisting of an aryl group, a substituted or unsubstituted silane group, a substituted or unsubstituted boron group, a substituted or unsubstituted germanium group, and a substituted or unsubstituted C ₅ to C ₆₀ heterocyclic group Or an unsubstituted C ₅ ~ C ₆₀ heterocyclic group; Or a condensed ring group of a C ₆ to C ₆₀ aromatic ring and a C ₄ to C ₆₀ aliphatic ring, each independently a hydrogen atom, a halogen atom, a substituted or unsubstituted aliphatic hydrocarbon group, a substituted or unsubstituted aryl group , A substituted and unsubstituted hetero aryl group. Compound represented by the following formula.

In the formula, R1 to R14 are the same as or different from each other, and each independently a halogen group, a C ₁ to C ₆₀ alkyl group, a C ₁ to C ₆₀ alkoxy group, a C ₁ to C ₆₀ alkylamine group, C ₁ to C ₆₀ arylamine group, C ₁ to C ₆₀ alkyl thiophene group, C ₆ to C ₆₀ aryl thiophene group, C ₂ to C ₆₀ alkenyl group, C ₂ to C ₆₀ alkynyl group, C ₃ to C ₆₀ cycloalkyl group, C ₆ ~ C ₆₀ aryl group, of a C ₆ ~ C ₆₀ substituted by deuterium aryl group, a C ₈ ~ C ₆₀ arylalkenyl group, a substituted or unsubstituted silane group, a substituted or unsubstituted ring of A C ₆ -C ₆₀ aryl group unsubstituted or substituted with one or more groups selected from the group consisting of a boron group, a substituted or unsubstituted germanium group, and a substituted or unsubstituted C ₅ -C ₆₀ heterocyclic group; Halogen, CN, NO ₂ , C ₁ to C ₆₀ alkyl group, C ₁ to C ₆₀ alkoxy group, C ₁ to C ₆₀ alkylamine group, C ₁ to C ₆₀ arylamine group, C ₁ to C ₆₀ the alkylthio group, C ₂ ~ C ₆₀ alkenyl group, C ₂ ~ C ₆₀ alkynyl group, C ₃ ~ C ₆₀ cycloalkyl group, C ₆ ~ C ₆₀ aryl group, a C ₆ ~ C ₆₀ substituted with a heavy hydrogen of the Substituted with one or more groups selected from the group consisting of an aryl group, a substituted or unsubstituted silane group, a substituted or unsubstituted boron group, a substituted or unsubstituted germanium group, and a substituted or unsubstituted C ₅ to C ₆₀ heterocyclic group Or an unsubstituted C ₅ ~ C ₆₀ heterocyclic group; Or a condensed ring group of a C ₆ to C ₆₀ aromatic ring and a C ₄ to C ₆₀ aliphatic ring, each independently a hydrogen atom, a halogen atom, a substituted or unsubstituted aliphatic hydrocarbon group, a substituted or unsubstituted aryl group , A substituted and unsubstituted hetero aryl group. The method of any of claims 1 to 3, wherein The R1 to R14 are adjacent compounds are bonded to each other to form a ring. The method according to any one of claims 1 to 3, The compound is one of the following compounds.

An organic electric device comprising at least one organic material layer comprising the compound of claim 1 or claim 3. The method of claim 6, The organic electroluminescent device, characterized in that to form the organic layer by the solution process (soluble process). The method of claim 6, The organic electroluminescent device is an organic electroluminescent device comprising a first electrode, the at least one organic material layer and the second electrode in a stacked form sequentially. The method of claim 8, The organic material layer is an organic electric element, characterized in that any one of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer and an electron injection layer. The method of claim 8, The organic material layer includes a light emitting layer, In the light emitting layer, the compound is used as a host or a dopant material. A display device comprising the organic electric element of claim 8; And a control unit for driving the display device. The method of claim 11, The organic electroluminescent device is an organic electroluminescent device (OLED), an organic solar cell, an organic photoconductor (OPC) drum, characterized in that one of the organic transistor (organic TFT).

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