KR101305934B1 - Chemical and Organic Electronic Element using the same, Terminal thereof - Google Patents

Abstract

The present invention provides a compound and an organic electric device using the same, and a terminal thereof.

Description

Compound and organic electronic device using same, terminal thereof {Chemical and Organic Electronic Element using the same, Terminal}

The present invention relates to a compound, an organic electric element 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. Here, in order to increase the efficiency and stability of the organic electronic device, the organic material layer may have a multi-layer structure composed of different materials, and may be formed 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 depending on the molecular weight, and may be classified into a phosphorescent material derived from singlet excited state of electrons and a phosphorescent material derived from the triplet excited state of electrons . 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. When the dopant having a smaller energy band gap than the host forming the light emitting layer is mixed with a small amount of the light emitting layer, the excitons generated in the light emitting layer are transported to the dopant to emit light with high efficiency. 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.

The present invention for solving the above problems of the background art hole injection material, hole transport material, suitable for fluorescence and phosphorescent devices of all colors, such as red, green, blue, white, according to the compound containing quinoxalinocarbazole It has been found to be useful as a luminescent material and / or an electron transporting material and as a host material for phosphorescent dopants of various colors, depending on the compound containing quinoxalinocarbazole.

Accordingly, an object of the present invention is to provide a compound containing quinoxalinocarbazole, an organic electronic device using the same, and an electronic device including the organic electronic device.

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

Accordingly, the present invention can provide a compound containing quinoxalinocarbazole, an organic electronic device using the same, and an electronic device or a terminal including the organic electronic device.

The present invention is useful as a hole injection material, a hole transport material, a light emitting material and / or an electron transport material suitable for fluorescence and phosphorescent devices of all colors such as red, green, blue and white depending on the compound containing quinoxalinocarbazole. In addition, depending on the compound containing quinoxalinocarbazole, it may exhibit a useful effect as a host material of phosphorescent dopants of various colors.

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

Hereinafter, some embodiments of the present invention will be described in detail with reference to 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 describing the components of the present invention, terms such as first, second, A, B, (a), and (b) may be used. These terms are intended to distinguish the constituent elements from other constituent elements, and the terms do not limit the nature, order or order of the constituent elements. When a component is described as being "connected", "coupled", or "connected" to another component, the component may be directly connected to or connected to the other component, It should be understood that an element may be "connected,""coupled," or "connected."

The present invention can provide a compound represented by the following formula (1).

Wherein R ₁ , R ₂ , R ₃ , R ₄ , R ₅ , R ₆ , R ₇ , R ₈ , R ₉ , R ₁₀ and R ₁₁ are each independently a hydrogen atom, a halogen atom, a cyano group, an alkoxy group, Thiol group, substituted or unsubstituted C1-C50 alkyl group, substituted or unsubstituted C1-C50 alkoxy group, substituted or unsubstituted C1-C50 alkenyl group, substituted or unsubstituted C5-C60 aryl A benzene group, a substituted or unsubstituted aryl group having 5 to 60 carbon atoms, a substituted or unsubstituted aryloxy group having 5 to 60 carbon atoms, sulfur (S), nitrogen (N), oxygen (O), phosphorus (P) and silicon At least one substituted or unsubstituted alkyl group having 1 to 50 carbon atoms or at least one sulfur (S), nitrogen (N), oxygen (O), phosphorus (P) and silicon (Si) A substituted or unsubstituted heteroaryl group having 5 to 60 carbon atoms or at least one containing sulfur (S), nitrogen (N), oxygen (O), phosphorus (P) and silicon (Si) Or beach can heteroaryloxy date of the ring carbon atoms of 5 to 60, but is not limited thereto.

Wherein R ₁ , R ₂ , R ₃ , R ₄ , R ₅ , R ₆ , R ₇ , R ₈ , R ₉ , R ₁₀ and R ₁₁ each combine with an adjacent group to form a substituted or unsubstituted saturated or unsaturated ring can do. For example, R ₁ and R ₂ , R ₂ and R ₃ , R ₄ and R ₅ , R ₅ and R ₆ , R ₆ and R ₇ , R ₈ and R ₉ , R ₉ and R ₁₀ , R ₁₀ and R ₁₁ May each combine with adjacent groups to form a substituted or unsubstituted saturated or unsaturated ring.

X is a hydrogen atom, a substituted or unsubstituted C1-C50 alkyl group, a substituted or unsubstituted C1-C50 alkenyl group, a substituted or unsubstituted C5-C60 arylene group, a substituted or unsubstituted C5-C5 Substitutes containing at least one aryl group of 60, a substituted or unsubstituted aryloxy group having 5 to 60 carbon atoms, sulfur (S), nitrogen (N), oxygen (O), phosphorus (P) and silicon (Si) Or a substituted or unsubstituted C 5 to 60 carbon atoms containing at least one unsubstituted alkyl group having 1 to 50 carbon atoms or sulfur (S), nitrogen (N), oxygen (O), phosphorus (P) and silicon (Si). Heteroaryl group or substituted or unsubstituted heteroaryloxy group having 5 to 60 carbon atoms containing at least one of sulfur (S), nitrogen (N), oxygen (O), phosphorus (P) and silicon (Si) However, it is not limited thereto.

Meanwhile, n may have an integer of 0 to 3, but is not limited thereto.

Meanwhile, the compound having the structural formula may be used in a solution process. In other words, the compound may form an organic material layer of an organic electric device, which will be described later, by a soluble process.

The present invention may provide a compound represented by one of the following Chemical Formulas 2 to 4. In Chemical Formulas 2 to 4, X may be the same as Chemical Formula 1, but is not limited thereto.

In this case, in Formulas 2 to 4, R ₁ , R ₂ , R ₃ , R ₄ , R ₅ , R ₆ , R ₇ , R ₈ , R ₉ , R ₁₀ and R ₁₁ may be the same as in Formula 1, but are not limited thereto. . Wherein R ₁ , R ₂ , R ₃ , R ₄ , R ₅ , R ₆ , R ₇ , R ₈ , R ₉ , R ₁₀ and R ₁₁ each combine with an adjacent group to form a substituted or unsubstituted saturated or unsaturated ring can do. For example, R ₁ and R ₂ , R ₂ and R ₃ , R ₄ and R ₅ , R ₅ and R ₆ , R ₆ and R ₇ , R ₈ and R ₉ , R ₉ and R ₁₀ , R ₁₀ and R ₁₁ May each combine with adjacent groups to form a substituted or unsubstituted saturated or unsaturated ring.

Compounds represented by Formulas 1 to 4 are specifically represented by the compound as shown in Formula 5 below, but is not limited thereto.

In addition, the substituents in Chemical Formulas 1 to 5 may be substituted or unsubstituted again even if not mentioned above, so that the substituents may be substituted with other substituents or substituents.

Various organic electric devices exist in which compounds including substituted or unsubstituted quinoxalinocarbazoles described with reference to Chemical Formulas 1 to 5 are used as the organic material layer. The organic electroluminescent device in which the compounds may be used for the substituted or unsubstituted quinoxalinocarbazole described with reference to Chemical Formulas 1 to 5 may be, for example, an organic light emitting diode (OLED), an organic solar cell, or an organic photoconductor (OPC) drum. And organic transistors (organic TFTs).

The organic electroluminescent device (OLED) is described as an example of the organic electroluminescent device to which the substituted or unsubstituted quinoxalinocarbazole described with reference to Chemical Formulas 1 to 5 can be applied, but the present invention is not limited thereto. The compounds described above may be applied to the organic electric device.

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 further includes a hole blocking layer (HBL) that blocks hole movement, an electron blocking layer (EBL) that blocks electrons from moving, a light emitting auxiliary layer that helps or assists light emission, and a protective layer. It may be located. The protective layer may be formed to protect the organic material layer or the cathode at the uppermost layer.

In this case, the substituted or unsubstituted quinoxalinocarbazole 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 containing a substituted or unsubstituted quinoxalinocarbazole described with reference to Formulas 1 to 5 may be 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, It may be used in place of one or more of the light emitting auxiliary layer and the protective layer, or may be used to form a layer with them. Of course, the organic layer may be used not only in one layer but also in two or more layers.

In particular, according to the compound containing substituted or unsubstituted quinoxalinocarbazole described with reference to Formulas 1 to 5, 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 It can be used as, in particular can be used as a host or dopant in the light emitting material and the host / dopant alone, can be used as a hole injection, a hole transport layer.

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.

An organic light emitting display device according to another embodiment of the present invention is a soluble process such as spin coating or ink jet process of the compound containing the substituted or unsubstituted quinoxalinocarbazole described above May be used.

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 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] (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 positioned thereon and capable of 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 containing 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, hole injection materials and holes suitable for fluorescence and phosphorescent devices of all colors, such as red, green, blue, and white, depending on the compound containing substituted or unsubstituted quinoxalinocarbazoles described with reference to Chemical Formulas 1 to 5 It can be used as a transport material, a light emitting material, an electron transport material and an electron injection material, and can be used as a host or dopant material of various colors.

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 control, 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, preparation or synthesis examples of the compounds including substituted or unsubstituted quinoxalinocarbazoles belonging to Chemical Formulas 1 to 5 will be described.

However, some of the compounds belonging to Formulas 1 to 5 will be exemplarily described because of the large number of compounds including substituted or unsubstituted quinoxalinocarbazoles belonging to Formulas 1 to 5. Those skilled in the art, that is, those skilled in the art, through the preparations described below, include two tertiary substituted or unsubstituted quinoxalinocarbazoles belonging to the invention which are not illustrated. Compound to make can be prepared.

Hereinafter, the compounds were synthesized according to the synthesis method described above, and the examples in which the compounds were applied to an organic material layer of an organic electroluminescent device, for example, an organic electroluminescent device, were compared with those of commonly used compounds.

First, a synthesis example of intermediates will be described.

 [Reaction Scheme 1]

Synthesis of intermediate A

Starting materials carbazole, 2-bromonitrobenzene, Pd ₂ (dba) ₃ , P ( t Bu) ₃ and NaO t Bu were dissolved in a toluene solvent and refluxed at 110 ° C. for 24 hours. After the reaction was completed, the reaction mixture was filtered under reduced pressure using celite and silica-gel using a hot toluene solvent. After cooling the temperature to room temperature, the precipitated product was recrystallized using toluene and acetone solvent to obtain the desired intermediate A (yield: 80%).

Synthesis of intermediate B

Intermediate A and PPh ₃ (triphenylphosphine) obtained in the above step was dissolved in o -DCB ( o -dichlorobenzene) and refluxed for 24 hours. At the end of the reaction, the solvent was removed using distillation under reduced pressure, and the concentrated product was separated using column chromatography to obtain the desired intermediate B (yield: 53%).

Hereinafter, synthesis examples of synthesizing compounds using the above-described intermediates will be described. Each synthesis example can be synthesized using intermediates or other compounds according to the respective schemes.

Synthesis of Compound 1

 [Reaction Scheme 2]

The intermediate B and iodobiphenyl, Pd ₂ (dba) ₃ , P ( t Bu) ₃ and NaO t Bu obtained in the above step were dissolved in a toluene solvent and refluxed at 110 ° C. for 24 hours. After the reaction was completed, the reaction mixture was filtered under reduced pressure using celite and silica-gel using a hot toluene solvent. The temperature was cooled to room temperature, and the precipitated product was recrystallized with toluene and acetone solvent to obtain desired compound 1 (yield: 68%).

Synthesis of Compound 16

 Scheme 3

After dissolving intermediate B and 2-chloro-4,6-diphenyl-1,3,5-triazine, Pd ₂ (dba) ₃ , P ( t Bu) ₃ and NaO t Bu obtained in the above step in a toluene solvent, 110 It was refluxed for 24 hours at ℃. After the reaction was completed, the reaction mixture was filtered under reduced pressure using celite and silica-gel using a hot toluene solvent.

After cooling the temperature to room temperature, the precipitated product was recrystallized using toluene and acetone solvent to obtain the desired compound 16 (yield: 45%).

Synthesis of Compound 25

 [Reaction Scheme 4]

Intermediate B and 2- (4-bromophenyl) -1-phenyl-1 H- benzo [ d ] imidazole, Pd ₂ (dba) ₃ , P ( t Bu) ₃ and NaO t Bu obtained in the above step were dissolved in a toluene solvent. It was then refluxed at 110 ° C. for 24 hours. After the reaction was completed, the reaction mixture was filtered under reduced pressure using celite and silica-gel using a hot toluene solvent. After cooling the temperature to room temperature, the precipitated product was recrystallized using a toluene and acetone solvent to give the desired compound 25 (yield: 61%).

Synthesis of Compound 29

 [Reaction Scheme 5]

Intermediate B and diiodobiphenyl, Pd ₂ (dba) ₃ , P ( t Bu) ₃ and NaO t Bu obtained in the above step were dissolved in a toluene solvent and refluxed at 110 ° C. for 24 hours. After the reaction was completed, the reaction mixture was filtered under reduced pressure using celite and silica-gel using a hot toluene solvent. After cooling the temperature to room temperature, the precipitated product was recrystallized using toluene and acetone solvent to obtain the desired compound 29 (yield: 56%).

Synthesis of Compound 30

 [Reaction Scheme 6]

The intermediate B and 1,3,5-tribromobenzene, Pd ₂ (dba) ₃ , P ( t Bu) ₃ and NaO t Bu obtained in the above step were dissolved in a toluene solvent and refluxed at 110 ° C. for 24 hours. After the reaction was completed, the reaction mixture was filtered under reduced pressure using celite and silica-gel using a hot toluene solvent. After cooling the temperature to room temperature, the precipitated product was recrystallized with toluene and acetone solvent to obtain the desired compound 30 (yield: 38%).

The organic electroluminescent device  Manufacturing evaluation

Compounds 1, 16, 25, 29, and 30 obtained through synthesis were used as light emitting host materials of the light emitting layer, thereby manufacturing an organic light emitting diode according to a conventional method.

A copper phthalocyanine (hereinafter abbreviated as CuPc) film was first vacuum deposited on the ITO layer (anode) formed on the glass substrate to form a thickness of 10 nm.

Subsequently, 4,4-bis [ N- (1-naphthyl) -N -phenylamino] biphenyl (abbreviated as a-NPD) was vacuum-deposited on the membrane as a hole transport compound to a thickness of 30 nm. A hole transport layer was formed. After the hole transport layer was formed, each of Compounds 1, 16, 25, 29 or 30 was deposited as a phosphorescent host material on the hole transport layer to form a light emitting layer.

At the same time, tris (2-phenylpyridine) iridium (abbreviated as I r (ppy) ₃ hereinafter) was added as a phosphorescent Ir metal complex dopant. At this time, the concentration of I r (ppy) _{3 in} the light emitting layer was 5% by weight. (1,1'bisphenyl) -4-oleato) bis (2-methyl-8-quinolineoleito) aluminum (hereinafter abbreviated as BAlq) was vacuum deposited to a thickness of 10 nm in a hole blocking layer, followed by electron Tris (8-quinolinol) aluminum (hereinafter abbreviated to Alq ₃ ) was formed into an injection 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

For comparison, instead of the compound of the present invention, a compound represented by the following formula (hereinafter abbreviated as CBP) was used as a light emitting host material to fabricate an organic light emitting display device having the same structure as that of the examples (synthesis examples).

Emitting layer
Host material Voltage
(V) Current density
(mA / cm ² ) Luminance
(cd / m ² ) Luminous efficiency
(cd / A) Chromaticity coordinates
(x, y) Example 1 Compound 1 5.8 0.31 106 43.3 (0.30, 0.60) Example 2 Compound 16 5.2 0.30 107 65.2 (0.32, 0.61) Example 3 Compound 25 5.3 0.30 105 62.3 (0.30, 0.60) Example 4 Compound 29 5.8 0.32 107 33.5 (0.31, 0.60) Example 5 Compound 30 5.9 0.31 103 48.3 (0.31, 0.60) Comparative Example 1 CBP 6.1 0.31 101 32.6 (0.33, 0.61)

As can be seen from the results of Table 1, the organic electroluminescent device using the compound for organic electroluminescent devices of the present invention is not only high efficiency and color purity is improved, but also a long life green light emission is obtained green phosphorescent host material of the organic light emitting device It can be used to significantly improve the luminous efficiency and lifetime.

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

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. It is therefore to be understood that the embodiments described above are to be considered in all respects only as illustrative and not restrictive. In addition, the scope of the present invention is indicated by the following claims rather than the detailed description. Also, all changes or modifications derived from the meaning and scope of the claims and their equivalents should be construed as being included within the scope of the present invention.

101: substrate 102: anode
103: hole injection layer 104: hole transport layer
105: light emitting layer 106: electron injection layer
107: electron transport layer 108: cathode

Claims (11)

Compound represented by the following formula:

here,
R ₁ , R ₂ , R ₃ , R ₄ , R ₅ , R ₆ , R ₇ , R ₈ , R ₉ , R ₁₀ and R ₁₁ are each independently a hydrogen atom,
X is a substituted or unsubstituted aryl group having 6 to 60 carbon atoms; A substituted or unsubstituted arylene group having 6 to 60 carbon atoms; And a substituted or unsubstituted heteroaryl group having 3 to 60 carbon atoms containing at least one sulfur (S), nitrogen (N), oxygen (O), phosphorus (P) and silicon (Si). Wherein in the case of X, a substituted aryl group, a substituted arylene group, or a substituted heteroaryl group, an alkyl group having 1 to 20 carbon atoms; Aryl groups having 6 to 20 carbon atoms; And a heteroaryl group having 3 to 20 carbon atoms including at least one hetero atom of O, N, S, Si, and P; and substituted with at least one substituent selected from the group consisting of:
N is an integer of 1 to 3. The method of claim 1,
Compound represented by the formula is a compound characterized in that the compound represented by one of the following formula.

The compound of claim 1, wherein the compound represented by Chemical Formula 1 is represented by one of the following Chemical Formulas.

delete An organic electric device comprising at least one organic material layer comprising the compound of any one of claims 1 to 3. The method of claim 5,
The organic electroluminescent device according to claim 1, wherein the organic layer is formed by a solution process. The method of claim 5,
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 7, wherein
The organic material layer is an organic electric device, 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, a light emitting layer. 9. The method of claim 8,
The light emitting layer is an organic electroluminescent device comprising the compound as a light emitting host material. A display device comprising the organic electric element of claim 5;
And a control unit for driving the display device. The method of claim 10,
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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