NOVEL COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE COMPRISING THE SAME

Abstract

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

Description

[Technical field]

[0001] [CROSS REFERENCE TO RELATED APPLICATIONS]

[0002] This application claims the benefit of priority based on Korean Patent Application No. 10-2021-0101385 dated August 2, 2021, and all contents disclosed in the documents of that Korean patent application are incorporated herein by reference.

[0003] The present invention relates to a novel compound and an organic light-emitting device containing the same. [Background technology]

[0004] Generally, organic light emitting phenomenon refers to a phenomenon in which electrical energy is converted into light energy using an organic material. Organic light emitting devices using the organic light emitting phenomenon have a wide viewing angle, excellent contrast, and fast response time, and are excellent in brightness, driving voltage, and response speed characteristics, and therefore many researches are being conducted on these devices.

[0005] An organic light-emitting device generally has a structure including a positive electrode, a negative electrode, and an organic layer between the positive electrode and the negative electrode. The organic layer is often a multi-layer structure composed of different materials to improve the efficiency and safety of the organic light-emitting device, for example, a hole injection layer, a hole transport layer, a light-emitting layer, an electron transport layer, an electron injection layer, etc. In such an organic light-emitting device structure, when a voltage is applied between two electrodes, holes are injected from the positive electrode and electrons are injected from the negative electrode into the organic layer. When the injected holes and electrons come into contact with each other, excitons are formed, and when the excitons fall back to the ground state, light is emitted.

[0006] There is a continuing demand for the development of new organic materials for use in such organic light-emitting devices. [Prior art documents] [Patent documents]

[0007] [Patent Document 1] Korean Patent Publication No. 10-2000-0051826 Summary of the Invention [Problem to be solved by the invention]

[0008] The present invention relates to a novel organic light-emitting material and an organic light-emitting device containing the same. [Means for solving the problem]

[0009] The present invention provides a compound represented by the following formula 1: [ka] In the above Chemical Formula 1, Ar1 and Ar2 each independently represent a substituted or unsubstituted aryl having 6 to 15 carbon atoms; R1 and R2 are each independently hydrogen or deuterium; n1 is an integer from 1 to 7; n2 is an integer from 1 to 6.

[0010] The present invention also provides an organic light-emitting device comprising: a first electrode; a second electrode provided opposite to the first electrode; and one or more organic layers provided between the first electrode and the second electrode, wherein at least one of the organic layers comprises a compound represented by Chemical Formula 1. Effect of the Invention

[0011] The compound represented by the above-mentioned Chemical Formula 1 can be used as a material for an organic layer of an organic light-emitting device, and can improve the efficiency, low driving voltage, and / or life characteristics of the organic light-emitting device. In particular, the compound represented by the above-mentioned Chemical Formula 1 can be used as a hole injection material, a hole transport material, a light-emitting material, an electron transport material, and / or an electron injection material. [Brief description of the drawings]

[0012] [Figure 1]1 is a diagram showing an example of an organic light-emitting device composed of a substrate 1, a positive electrode 2, a light-emitting layer 3, and a negative electrode 4. FIG. [Diagram 2] 1 shows an example of an organic light-emitting device consisting of a substrate 1, a positive electrode 2, a hole injection layer 5, a hole transport layer 6, an electron blocking layer 7, a light-emitting layer 3, an electron injection and transport layer 8, and a negative electrode 4. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0013] The present invention will now be described in more detail to aid in its understanding.

[0014] The present invention provides a compound represented by Chemical Formula 1.

[0015] In this specification, [ka] or [ka] denotes a bond that is connected to another substituent.

[0016] In the present specification, the term "substituted or unsubstituted" means that the group is substituted or unsubstituted with one or more substituents selected from the group consisting of deuterium; halogen group; nitrile group; nitro group; hydroxy group; carbonyl group; ester group; imide group; amino group; phosphine oxide group; alkoxy group; aryloxy group; alkylthiooxy group; arylthiooxy group; alkylsulfoxy group; arylsulfoxy group; silyl group; boron group; alkyl group; cycloalkyl group; alkenyl group; aryl group; aralkyl group; aralkenyl group; alkylaryl group; alkylamine group; aralkylamine group; heteroarylamine group; arylamine group; arylphosphine group; or heteroaryl group containing one or more of N, O and S atoms, or that the group is substituted or unsubstituted with two or more of the above-mentioned exemplified substituents connected to each other. For example, the "substituent having two or more substituents connected to each other" may be a biphenyl group. That is, the biphenyl group may be an aryl group, and can be interpreted as a substituent having two phenyl groups connected to each other.

[0017] In this specification, the number of carbon atoms in the carbonyl group is not particularly limited, but the carbon number is preferably 1 to 40. Specifically, the carbonyl group may have a substituent having the following structure, but is not limited thereto. [ka]

[0018] In the present specification, the oxygen of the ester group may be substituted with a linear, branched or cyclic alkyl group having 1 to 25 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Specifically, the substituent may be one of the following structural formulas, but is not limited thereto. [ka]

[0019] In this specification, the number of carbon atoms of the imido group is not particularly limited, but is preferably 1 to 25. Specifically, the imido group may have a substituent having the following structure, but is not limited thereto. [ka]

[0020] In this specification, specific examples of the silyl group include a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a vinyldimethylsilyl group, a propyldimethylsilyl group, a triphenylsilyl group, a diphenylsilyl group, a phenylsilyl group, and the like, but are not limited to these.

[0021] In this specification, specific examples of the boron group include a trimethyl boron group, a triethyl boron group, a t-butyl dimethyl boron group, a triphenyl boron group, a phenyl boron group, and the like, but are not limited thereto.

[0022] As used herein, examples of halogen groups include fluorine, chlorine, bromine, or iodine.

[0023] In this specification, the alkyl group may be linear or branched, and the number of carbon atoms is not particularly limited, but is preferably 1 to 40. According to one embodiment, the number of carbon atoms of the alkyl group is 1 to 20. According to yet another embodiment, the number of carbon atoms of the alkyl group is 1 to 10. According to yet another embodiment, the number of carbon atoms of the alkyl group is 1 to 6. Specific examples of alkyl groups include, but are not limited to, methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl, n-heptyl, 1-methylhexyl, cyclopentylmethyl, cyclohexylmethyl, octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhexyl, 2-propylpentyl, n-nonyl, 2,2-dimethylheptyl, 1-ethyl-propyl, 1,1-dimethyl-propyl, isohexyl, 2-methylpentyl, 4-methylhexyl, 5-methylhexyl, and the like.

[0024] In this specification, the alkenyl group may be linear or branched, and the number of carbon atoms is not particularly limited, but is preferably 2 to 40. According to one embodiment, the number of carbon atoms of the alkenyl group is 2 to 20. According to yet another embodiment, the number of carbon atoms of the alkenyl group is 2 to 10. According to yet another embodiment, the number of carbon atoms of the alkenyl group is 2 to 6. Specific examples include, but are not limited to, vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 3-methyl-1-butenyl, 1,3-butadienyl, allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, 2,2-diphenylvinyl-1-yl, 2-phenyl-2-(naphthyl-1-yl)vinyl-1-yl, 2,2-bis(diphenyl-1-yl)vinyl-1-yl, a stilbenyl group, and a styrenyl group.

[0025] In the present specification, the cycloalkyl group is not particularly limited, but preferably has 3 to 60 carbon atoms, and in one embodiment, the cycloalkyl group has 3 to 30 carbon atoms. In another embodiment, the cycloalkyl group has 3 to 20 carbon atoms. In another embodiment, the cycloalkyl group has 3 to 6 carbon atoms. Specific examples include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, 3-methylcyclopentyl, 2,3-dimethylcyclopentyl, cyclohexyl, 3-methylcyclohexyl, 4-methylcyclohexyl, 2,3-dimethylcyclohexyl, 3,4,5-trimethylcyclohexyl, 4-tert-butylcyclohexyl, cycloheptyl, and cyclooctyl.

[0026] In the present specification, the aryl group is not particularly limited, but preferably has 6 to 60 carbon atoms, and may be a monocyclic aryl group or a polycyclic aryl group. According to one embodiment, the aryl group has 6 to 30 carbon atoms. According to one embodiment, the aryl group has 6 to 20 carbon atoms. The monocyclic aryl group may be, but is not limited to, a phenyl group, a biphenyl group, a terphenyl group, etc. The polycyclic aryl group may be, but is not limited to, a naphthyl group, an anthracenyl group, a phenanthryl group, a pyrenyl group, a perylenyl group, a chrysenyl group, a fluorenyl group, etc.

[0027] In this specification, the fluorenyl group may be substituted, and two of the substituents may be bonded together to form a spiro structure. When the fluorenyl group is substituted, [ka] However, the present invention is not limited to these.

[0028] In the present specification, the heteroaryl group is a heteroaryl group containing one or more of O, N, Si and S as a hetero element, and the number of carbon atoms is not particularly limited, but preferably has 2 to 60 carbon atoms. According to one embodiment, the number of carbon atoms of the heteroaryl group is 6 to 30. According to one embodiment, the number of carbon atoms of the heteroaryl group is 6 to 20. Examples of heteroaryl groups include, but are not limited to, thiophene, furan, pyrrole, imidazole, thiazole, oxazole, oxadiazole, triazole, pyridyl, bipyridyl, pyrimidyl, triazine, acridyl, pyridazine, pyrazinyl, quinolinyl, quinazoline, quinoxalinyl, phthalazinyl, pyridopyrimidinyl, pyridopyrazinyl, pyrazinopyrazinyl, isoquinoline, indole, carbazole, benzoxazole, benzimidazole, benzothiazole, benzocarbazole, benzothiophene, dibenzothiophene, benzofuranyl, phenanthroline, isoxazolyl, thiadiazolyl, phenothiazinyl, and dibenzofuranyl.

[0029] In this specification, the above-mentioned explanation regarding the aryl group is applicable to the aryl group in the aralkyl group, the aralkenyl group, the alkylaryl group, and the arylamine group. In this specification, the above-mentioned explanation regarding the alkyl group is applicable to the alkyl group in the aralkyl group, the alkylaryl group, and the alkylamine group. In this specification, the above-mentioned explanation regarding the heteroaryl group is applicable to the heteroaryl in the heteroarylamine. In this specification, the above-mentioned explanation regarding the alkenyl group is applicable to the alkenyl group in the aralkenyl group. In this specification, the above-mentioned explanation regarding the aryl group is applicable to the arylene, except that it is a divalent group. In this specification, the above-mentioned explanation regarding the heteroaryl group is applicable to the heteroarylene, except that it is a divalent group. In this specification, the above-mentioned explanation regarding the aryl group or the cycloalkyl group is applicable to the hydrocarbon ring, except that it is not a monovalent group but is formed by bonding two substituents. In this specification, the above-mentioned explanation regarding the heteroaryl group is applicable to the heteroaryl, except that it is not a monovalent group but is formed by bonding two substituents.

[0030] Preferably, the chemical formula 1 is represented by any one of the following chemical formulas 1-1 to 1-6: [ka] [ka]

[0031] In the above Chemical Formulas 1-1 to 1-6, Ar1, Ar2, R1, R2, n1 and n2 are as defined in Chemical Formula 1 above.

[0032] Preferably, Ar1 and Ar2 may each independently be an aryl having 6 to 14 carbon atoms that is unsubstituted or substituted with deuterium. More preferably, Ar1 and Ar2 may each independently be phenyl, phenyl substituted with 3 or 5 deuteriums, biphenylyl, biphenylyl substituted with 5 or 9 deuteriums, naphthyl, naphthyl substituted with 7 deuteriums, phenanthrenyl, or phenanthrenyl substituted with 9 deuteriums. Most preferably, Ar1 and Ar2 may each independently be any one selected from the group consisting of: [ka]

[0033] Preferably, Ar 1 may be any one selected from the group consisting of: [ka]

[0034] Preferably, each Ar2 is independently phenyl, phenyl substituted with 5 deuteriums, biphenylyl, biphenylyl substituted with 5 or 9 deuteriums, naphthyl, naphthyl substituted with 7 deuteriums, or phenanthrenyl. More preferably, Ar2 may be any one selected from the group consisting of: [ka]

[0035] Preferably, at least one of Ar1 and Ar2 may be phenyl or phenyl substituted with 3 or 5 deuteriums.

[0036] Representative examples of the compound represented by Formula 1 are as follows:

[0037] [ka]

[0038] [ka]

[0039] [ka]

[0040] [ka]

[0041] [ka]

[0042] [ka]

[0043] [ka]

[0044] [ka]

[0045] [ka]

[0046] The compound represented by Chemical Formula 1 can be prepared, for example, by the method of Reaction Scheme 1 below, and the remaining compounds can be prepared by similar methods. [ka] In the above reaction formula 1, Ar1, Ar2, R1, R2, n1 and n2 are as defined in the above chemical formula 1, and X is a halogen, preferably, X is chloro or bromo.

[0047] The reaction scheme 1 is a Suzuki coupling reaction, which is preferably carried out in the presence of a palladium catalyst and a base, and the reactive group for the Suzuki coupling reaction can be changed within the range known in the art. The preparation method is more specifically described in the preparation examples described below.

[0048] The present invention also provides an organic light-emitting device comprising the compound represented by Chemical Formula 1. For example, the present invention provides an organic light-emitting device comprising a first electrode, a second electrode provided opposite to the first electrode, and one or more organic material layers provided between the first electrode and the second electrode, wherein at least one of the organic material layers comprises the compound represented by Chemical Formula 1.

[0049] The organic layer of the organic light-emitting device of the present invention may have a single-layer structure, or may have a multi-layer structure in which two or more organic layers are laminated. For example, the organic light-emitting device of the present invention may have a structure including a hole injection layer, a hole transport layer, a light-emitting layer, an electron transport layer, an electron injection layer, etc. as the organic layer. However, the structure of the organic light-emitting device is not limited thereto, and may include a smaller number of organic layers.

[0050] In addition, the organic layer may further include a light-emitting layer, and the light-emitting layer may include the compound represented by Chemical Formula 1.

[0051] In addition, the organic layer may include a hole transport layer, a hole injection layer, or a layer that simultaneously transports and injects holes, and the hole transport layer, the hole injection layer, or the layer that simultaneously transports and injects holes may include a compound represented by Chemical Formula 1.

[0052] In addition, the organic layer may include an electron transport layer, an electron injection layer, or an electron injection and transport layer, and the electron transport layer, the electron injection layer, or the electron injection and transport layer may include a compound represented by Chemical Formula 1.

[0053] The organic light-emitting device according to the present invention may be an organic light-emitting device having a structure (normal type) in which a positive electrode, one or more organic layers, and a negative electrode are sequentially stacked on a substrate. The organic light-emitting device according to the present invention may be an organic light-emitting device having an inverted structure (inverted type) in which a negative electrode, one or more organic layers, and a positive electrode are sequentially stacked on a substrate. For example, the structure of an organic light-emitting device according to an embodiment of the present invention is illustrated in FIG. 1 and FIG. 2.

[0054] Fig. 1 is a diagram showing an example of an organic light-emitting device consisting of a substrate 1, a positive electrode 2, an emitting layer 3, and a negative electrode 4. Fig. 2 is a diagram showing an example of an organic light-emitting device consisting of a substrate 1, a positive electrode 2, a hole injection layer 5, a hole transport layer 6, an electron blocking layer 7, an emitting layer 3, an electron injection and transport layer 8, and a negative electrode 4. In this structure, the compound represented by Chemical Formula 1 may be contained in the emitting layer.

[0055] The organic light emitting device according to the present invention may be manufactured using materials and methods known in the art, except that at least one of the organic layers contains the compound represented by Chemical Formula 1. In addition, when the organic light emitting device includes a plurality of organic layers, the organic layers may be formed of the same material or different materials.

[0056] For example, the organic light emitting device according to the present invention may be manufactured by sequentially stacking a first electrode, an organic layer, and a second electrode on a substrate. In this case, a metal or a conductive metal oxide or an alloy thereof may be deposited on a substrate using a physical vapor deposition (PVD) method such as sputtering or e-beam evaporation to form a cathode, and an organic layer including a hole injection layer, a hole transport layer, an emission layer, and an electron transport layer may be formed thereon, and a material to be used as an anode may be deposited thereon. In addition to this method, an organic light emitting device may be manufactured by sequentially depositing an anode material, an organic layer, and an anode material on a substrate.

[0057] In addition, the compound represented by Formula 1 may be formed as an organic layer by a solution coating method as well as a vacuum deposition method during the preparation of an organic light emitting device, where the solution coating method refers to, but is not limited to, spin coating, dip coating, doctor blading, ink jet printing, screen printing, spraying, roll coating, etc.

[0058] In addition to these methods, an organic light-emitting device can be manufactured by sequentially depositing a negative electrode material, an organic layer, and a positive electrode material on a substrate (WO2003 / 012890). However, the manufacturing method is not limited to these.

[0059] For example, the first electrode is a positive electrode and the second electrode is a negative electrode, or the first electrode is a negative electrode and the second electrode is a positive electrode.

[0060] The cathode material is preferably a material having a large work function so that hole injection in the organic layer can be facilitated.Specific examples of the cathode material include, but are not limited to, metals such as vanadium, chromium, copper, zinc, and gold, or alloys thereof; metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO); combinations of metals and oxides such as ZnO:Al or SnO2:Sb; and conductive polymers such as poly(3-methylthiophene), poly[3,4-(ethylene-1,2-dioxy)thiophene] (PEDOT), polypyrrole, and polyaniline.

[0061] The negative electrode material is preferably a material having a small work function so that electrons can be easily injected into the organic layer. Specific examples of the negative electrode material include, but are not limited to, metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin, and lead, or alloys thereof; and multilayer structures such as LiF / Al or LiO2 / Al.

[0062] The hole injection layer is a layer that injects holes from the electrode, and the hole injection material is preferably a compound that has the ability to transport holes, has a hole injection effect at the positive electrode, has an excellent hole injection effect on the light emitting layer or light emitting material, prevents the movement of excitons generated in the light emitting layer to the electron injection layer or electron injection material, and has excellent thin film forming ability. The HOMO (highest occupied molecular orbital) of the hole injection material is preferably between the work function of the positive electrode material and the HOMO of the surrounding organic layer. Specific examples of the hole injection material include metal porphyrin, oligothiophene, arylamine-based organic materials, hexanitrile hexaazatriphenylene-based organic materials, quinacridone-based organic materials, perylene-based organic materials, anthraquinone, and polyaniline and polythiophene-based conductive polymers, but are not limited thereto.

[0063] The hole transport layer is a layer that receives holes from the hole injection layer and transports them to the light emitting layer, and the hole transport material is a material that can receive holes from the positive electrode or the hole injection layer and move them to the light emitting layer, and is preferably a material that has high mobility for holes.Specific examples include, but are not limited to, arylamine-based organic materials, conductive polymers, and block copolymers in which both conjugated and non-conjugated parts exist.

[0064] The electron blocking layer is a layer placed between the hole transport layer and the light emitting layer to prevent the electrons injected from the negative electrode from passing to the hole transport layer without being recombined in the light emitting layer, and is also called an electron inhibiting layer. For the electron blocking layer, a material having a smaller electron affinity than that of the electron transport layer is preferable.

[0065] The light-emitting material is preferably a material that can emit light in the visible light region by receiving and combining holes and electrons transported from the hole transport layer and electron transport layer, and has good quantum efficiency for fluorescence and phosphorescence.Specific examples include, but are not limited to, 8-hydroxy-quinoline aluminum complex (Alq3), carbazole-based compounds, dimerized styryl compounds, BAlq, 10-hydroxybenzoquinoline-metal compounds, benzoxazole, benzothiazole and benzimidazole-based compounds, poly(p-phenylenevinylene) (PPV)-based polymers, spiro compounds, polyfluorene, rubrene, etc.

[0066] The light-emitting layer may include a host material and a dopant material. The host material may be a fused aromatic ring derivative or a heterocyclic ring-containing compound. Specifically, the fused aromatic ring derivative may be an anthracene derivative, a pyrene derivative, a naphthalene derivative, a pentacene derivative, a phenanthrene compound, a fluoranthene compound, and the heterocyclic ring-containing compound may be, but is not limited to, a carbazole derivative, a dibenzofuran derivative, a ladder-type furan compound, a pyrimidine derivative, and the like. In particular, the compound according to the present invention is used as a host material of the light-emitting layer.

[0067] The dopant materials include aromatic amine derivatives, styrylamine compounds, boron complexes, fluoranthene compounds, metal complexes, etc. Specifically, the aromatic amine derivatives are condensed aromatic ring derivatives having substituted or unsubstituted arylamino groups, such as pyrene, anthracene, chrysene, and periflanthene, which have arylamino groups, and the styrylamine compounds are compounds in which at least one arylvinyl group is substituted on a substituted or unsubstituted arylamine, and one or more substituents selected from the group consisting of an aryl group, a silyl group, an alkyl group, a cycloalkyl group, and an arylamino group are substituted or unsubstituted. Specifically, the dopant materials include, but are not limited to, styrylamine, styryldiamine, styryltriamine, and styryltetraamine. In addition, the metal complexes include, but are not limited to, iridium complexes and platinum complexes.

[0068] The electron transport layer is a layer that receives electrons from the electron injection layer and transports them to the light-emitting layer. The electron transport material is preferably a material that can receive electrons from the negative electrode well and transfer them to the light-emitting layer, and has high mobility for electrons. Specific examples include, but are not limited to, Al complexes of 8-hydroxyquinoline; complexes containing Alq3; organic radical compounds; and hydroxyflavone-metal complexes. The electron transport layer can be used with any desired cathode material, as used according to the prior art. In particular, examples of suitable cathode materials are conventional materials that have a low work function and are followed by an aluminum or silver layer. Specific examples are cesium, barium, calcium, ytterbium, and samarium, each of which is followed by an aluminum or silver layer.

[0069] The electron injection layer is a layer that injects electrons from an electrode, and is capable of transporting electrons, has an excellent electron injection effect from a negative electrode, an excellent electron injection effect for the light-emitting layer or light-emitting material, prevents the excitons generated in the light-emitting layer from moving to the hole injection layer, and is preferably a compound with excellent thin-film forming ability.Specific examples include, but are not limited to, fluorenone, anthraquinone dimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylene tetracarboxylic acid, preolenylidene methane, anthrone, etc., and their derivatives, metal complex compounds, and nitrogen-containing five-membered ring derivatives.

[0070] Examples of the metal complex compound include, but are not limited to, 8-hydroxyquinolinato lithium, bis(8-hydroxyquinolinato) zinc, bis(8-hydroxyquinolinato) copper, bis(8-hydroxyquinolinato) manganese, tris(8-hydroxyquinolinato) aluminum, tris(2-methyl-8-hydroxyquinolinato) aluminum, tris(8-hydroxyquinolinato) gallium, bis(10-hydroxybenzo[h]quinolinato) beryllium, bis(10-hydroxybenzo[h]quinolinato) zinc, bis(2-methyl-8-quinolinato) chlorogallium, bis(2-methyl-8-quinolinato) (o-cresolato) gallium, bis(2-methyl-8-quinolinato) (1-naphtholato) aluminum, and bis(2-methyl-8-quinolinato) (2-naphtholato) gallium.

[0071] Meanwhile, in the present invention, the "electron injection and transport layer" is a layer that serves both the functions of the electron injection layer and the electron transport layer, and the materials serving as the respective layers may be used alone or in combination, but are not limited thereto.

[0072] The organic light emitting device according to the present invention may be a bottom emission device, a top emission device, or a dual emission device, and may be a bottom emission device which is particularly required to have a relatively high light emitting efficiency.

[0073] In addition, the compound represented by Formula 1 can be included in an organic solar cell or an organic transistor in addition to the organic light emitting device.

[0074] The present invention will be described in more detail below to help understanding of the present invention, however, the following examples are merely illustrative of the present invention and are not intended to limit the scope of the present invention. EXAMPLES

[0075] [Production Example] Production Example 1: Synthesis of Compound 1 [ka] In a nitrogen atmosphere, 2-([1,1'-biphenyl]-4-yl)-4-chloro-6-(dibenzo[b,d]furan-1-yl)-1,3,5-triazine (15.0g, 34.6mmol) and 4,4,5,5-tetramethyl-2-(6-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane (12.6g, 38.0mmol) were added to 300ml of THF and stirred and refluxed. Then, potassium carbonate (19.1g, 138.3mmol) was dissolved in 57ml of water and added, and after stirring thoroughly, tetrakis(triphenylphosphine)palladium(0) (0.1g, 1.0mmol) was added. After reacting for 10 hours, the mixture was cooled to room temperature, the organic layer and the aqueous layer were separated, and the organic layer was distilled. This was dissolved again in chloroform and washed twice with water, after which the organic layer was separated, anhydrous magnesium sulfate was added and stirred, then filtered and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography, and then 7.5 g of compound 1 was produced by sublimation purification (yield 36%, MS: [M+H] + =603).

[0076] Production Example 2: Synthesis of Compound 2 [ka] Compound 2 was prepared in the same manner as in Preparation Example 1, except that 2-([1,1'-biphenyl]-4-yl)-4-chloro-6-(dibenzo[b,d]furan-1-yl)-1,3,5-triazine was replaced with 2-chloro-4-(dibenzo[b,d]furan-1-yl)-6-phenyl-1,3,5-triazine and 4,4,5,5-tetramethyl-2-(6-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane was replaced with 2-([2,2'-binaphthalen]-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (MS: [M+H] + =577).

[0077] Production Example 3: Synthesis of Compound 3 [ka] Compound 3 was prepared in the same manner as Compound 1, except that 2-([1,1'-biphenyl]-4-yl)-4-chloro-6-(dibenzo[b,d]furan-1-yl)-1,3,5-triazine was used instead of 2-chloro-4-(dibenzo[b,d]furan-1-yl)-6-(naphthalen-2-yl)-1,3,5-triazine in Preparation Example 1 (MS: [M+H] + =577).

[0078] Production Example 4: Synthesis of Compound 4 [ka] Compound 4 was prepared in the same manner as in Preparation Example 1, except that 2-([1,1'-biphenyl]-4-yl)-4-chloro-6-(dibenzo[b,d]furan-1-yl)-1,3,5-triazine was replaced with 2-chloro-4-(dibenzo[b,d]furan-1-yl)-6-phenyl-1,3,5-triazine and 4,4,5,5-tetramethyl-2-(6-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane was replaced with 2-([1,2'-binaphthalen]-6'-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (MS: [M+H] + =577).

[0079] Production Example 5: Synthesis of Compound 5 [ka] Compound 5 was prepared in the same manner as Compound 1, except that in Preparation Example 1, 2-([1,1'-biphenyl]-4-yl)-4-chloro-6-(dibenzo[b,d]furan-1-yl)-1,3,5-triazine was replaced with 2-chloro-4-(dibenzo[b,d]furan-1-yl)-6-(phenanthren-3-yl)-1,3,5-triazine, and 4,4,5,5-tetramethyl-2-(6-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane was replaced with 4,4,5,5-tetramethyl-2-(7-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane. (MS: [M+H] + =627)

[0080] Production Example 6: Synthesis of Compound 6 [ka] Compound 6 was prepared in the same manner as Compound 1, except that in Preparation Example 1, 2-([1,1'-biphenyl]-4-yl)-4-chloro-6-(dibenzo[b,d]furan-1-yl)-1,3,5-triazine was replaced with 2-([1,1'-biphenyl]-3-yl)-4-chloro-6-(dibenzo[b,d]furan-1-yl)-1,3,5-triazine, and 4,4,5,5-tetramethyl-2-(6-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane was replaced with 4,4,5,5-tetramethyl-2-(4-phenylnaphthalen-2-yl)-1,3,2-dioxaborolane. (MS: [M+H] + =603)

[0081] Production Example 7: Synthesis of Compound 7 [ka] In a nitrogen atmosphere, 2-chloro-4-(naphthalen-1-yl-d7)-6-(6-phenylnaphthalen-2-yl)-1,3,5-triazine (15g, 33.3mmol) and dibenzo[b,d]furan-1-ylboronic acid (7.8g, 36.6mmol) were added to 300ml of THF and stirred and refluxed. Then, potassium carbonate (18.4g, 133mmol) was dissolved in 55ml of water and added, and after stirring thoroughly, tetrakis(triphenylphosphine)palladium(0) (0.1g, 1mmol) was added. After 9 hours of reaction, the mixture was cooled to room temperature, the organic layer and the aqueous layer were separated, and the organic layer was distilled. This was dissolved again in chloroform and washed twice with water, and the organic layer was separated, anhydrous magnesium sulfate was added, stirred, filtered, and the filtrate was distilled under reduced pressure. The concentrated compound was purified by silica gel column chromatography to produce 8.1 g of compound 7. (Yield 42%, MS: [M+H] + =584)

[0082] Production Example 8: Synthesis of Compound 8 [ka] Compound 8 was prepared in the same manner as in Preparation Example 7, except that 2-chloro-4-(naphthalen-1-yl-d7)-6-(6-phenylnaphthalen-2-yl)-1,3,5-triazine was replaced with 2-([1,1'-biphenyl]-4-yl)-4-chloro-6-(7-phenylnaphthalen-2-yl)-1,3,5-triazine and dibenzo[b,d]furan-1-ylboronic acid was replaced with (dibenzo[b,d]furan-1-yl-d7)boronic acid (MS: [M+H] + =610).

[0083] [Example] Comparative Example 1 A glass substrate coated with a 1400 Å thick thin film of ITO (Indium Tin Oxide) was soaked in distilled water with detergent and ultrasonically cleaned. The detergent used was Decon (Fischer Co.). TM (registered trademark) CON705 product was used, and distilled water was filtered through a 0.22 μm sterilizing filter manufactured by Millipore Co. The ITO was washed for 30 minutes, and then ultrasonically cleaned twice with distilled water for 10 minutes. After the distilled water cleaning was completed, the substrate was ultrasonically cleaned for 10 minutes each with isopropyl alcohol, acetone, and methanol solvents, dried, and then transferred to a plasma cleaning device. The substrate was also cleaned for 5 minutes using oxygen plasma, and then transferred to a vacuum deposition device.

[0084] On the ITO transparent electrode thus prepared, the following compound HI-A and compound LG-101 were sequentially thermally vacuum deposited to a thickness of 800 Å and 50 Å, respectively, to form a hole injection layer. On top of that, the following compound HT-A was vacuum deposited to a thickness of 800 Å as a hole transport layer, and then the following compound EB-A was thermally vacuum deposited to a thickness of 600 Å as an electron blocking layer. Compound RH-A was applied as a host for the light-emitting layer, and compound RD-A was applied as a dopant, and the host and dopant were vacuum deposited to a thickness of 400 Å in a weight ratio of 98:2. Then, the following compound ET-A and compound Liq were thermally vacuum deposited to a thickness of 360 Å in a ratio of 1:1 as an electron transport and injection layer, and Liq was then vacuum deposited to a thickness of 5 Å.

[0085] Magnesium and silver were sequentially deposited on the electron injection layer in a ratio of 10:1 to a thickness of 220 Å, and aluminum was deposited to a thickness of 1000 Å to form a negative electrode, thereby completing the manufacture of an organic light emitting device.

[0086] [ka]

[0087] During the above process, the deposition rate of the organic material was maintained at 0.4-0.7 Å / sec, the deposition rate of magnesium and silver was maintained at 2 Å / sec, and the vacuum degree during deposition was 2×10 -7 ~5×10 -6 Torr was maintained to fabricate an organic light-emitting device.

[0088] Examples 1 to 16 and Comparative Examples 2 to 6 Organic light emitting devices of Examples 1 to 16 and Comparative Examples 2 to 6 were manufactured using the same method as in Comparative Example 1, except that the light emitting layer host was changed to the compound in Table 1 instead of Compound 1 in Comparative Example 1. In this case, when a mixture of two compounds was used as the host, the weight ratio between the host compounds is indicated in parentheses. Compounds pRH-1, pRH-2 and compounds A to C in Table 1 are as follows.

[0089] [ka]

[0090] [Experimental Example] A current was applied to the organic light emitting devices fabricated in Examples 1 to 16 and Comparative Examples 1 to 6, and the voltage, efficiency, and lifespan were measured, and the results are shown in Table 2 below. At this time, the voltage and efficiency were 10 mA / cm 2 The LT97 is measured at a current density of 20mA / cm 2 This means the time it takes for the initial brightness to decrease to 97%.

[0091] [Table 1]

[0092] From the results of Table 1, it was confirmed that when the compound having the structure of Chemical Formula 1 is applied to the light emitting layer of an organic electroluminescent device, a device having low voltage, high efficiency, and long life characteristics can be obtained. [Explanation of symbols]

[0093] 1. Substrate 2...Positive electrode 3. Emitting layer 4...Negative electrode 5. Hole injection layer 6. Hole transport layer 7...electron blocking layer 8. Electron injection and transport layer

Claims

1. A compound represented by the following chemical formula 1: 【Chemistry 1】 In the above Chemical Formula 1, Ar １ and Ar ２ each independently represents an unsubstituted or deuterium-substituted aryl having 6 to 14 carbon atoms; R １ and R ２ are each independently hydrogen or deuterium; n1 is an integer from 1 to 7; n2 is an integer from 1 to 6; However, the following compounds are excluded from the compounds represented by Chemical Formula 1: 【Chemistry 5】 。

2. The compound according to claim 1, wherein the chemical formula 1 is represented by any one of the following chemical formulas 1-1 to 1-6: 【Chemistry 2A】 【Chemistry 2B】 In the above Chemical Formula 1-1 to Chemical Formula 1-6, Ar １ , Ar ２ , R １ , R ２ , n1 and n2 are as defined in claim 1.

3. Ar １ and Ar ２ are each independently phenyl, phenyl substituted with 3 or 5 deuteriums, biphenylyl, biphenylyl substituted with 5 or 9 deuteriums, naphthyl, naphthyl substituted with 7 deuteriums, phenanthrenyl, or phenanthrenyl substituted with 9 deuteriums.

4. Ar １ and Ar ２ is independently any one selected from the group consisting of: 【Chemistry 3】 。

5. Ar １ and Ar ２ 2. The compound of claim 1, wherein at least one of is phenyl or phenyl substituted with 3 or 5 deuteriums.

6. The compound according to claim 1, wherein the compound represented by Chemical Formula 1 is any one selected from the group consisting of: 【Chemistry 4A】 【Chemistry 4B】 【Chemistry 4C】 【Chemistry 4D】 【Chemistry 4E】 [Chemical formula 4F] [Chem 4G] 【Chemical 4H】 【Chemistry 4I】 。

7. An organic light-emitting device comprising: a first electrode; a second electrode provided opposite to the first electrode; and one or more organic material layers provided between the first electrode and the second electrode, wherein one or more of the organic material layers comprises the compound according to any one of claims 1 to 6.

8. The organic light-emitting device according to claim 7 , wherein the organic layer is a light-emitting layer.

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