KR20230041202A - Novel compound, ink composition comprising same, organic light emitting device comprising same and method of manufacturing same - Google Patents

Abstract

The present invention relates to a compound represented by a chemical formula 1, an ink composition including the compound represented by the chemical formula 1, an organic light emitting device using the same, and a manufacturing method thereof. The compound represented by the chemical formula 1 of the present invention can be used as a material for an organic material layer of an organic light emitting device, and a device having low driving voltage, excellent efficiency characteristics and/or excellent lifespan characteristics can be obtained.

Description

A novel compound, an ink composition containing the same, an organic light emitting device including the same, and a manufacturing method thereof

The present invention relates to a novel compound, an ink composition containing the compound, an organic light emitting device formed using the ink composition, and a method for manufacturing the same.

The organic light emitting phenomenon is one example in which electric current is converted into visible light by an internal process of specific organic molecules. The principle of the organic light emitting phenomenon is as follows. When the organic material layer is placed between the anode and the cathode, when a current is applied between the two electrodes, electrons and holes are injected into the organic material layer from the cathode and the anode, respectively. Electrons and holes injected into the organic material layer recombine to form excitons, and the excitons fall back to the ground state and emit light. An organic light emitting device using this principle may generally be composed of a cathode, an anode, and organic material layers disposed therebetween, such as a hole injection layer, a hole transport layer, a light emitting layer, an electron injection layer, and an electron transport layer.

Conventionally, a deposition process has been mainly used to manufacture an organic light emitting device. However, when manufacturing an organic light emitting device using a deposition process, there are problems that a lot of material loss occurs and it is difficult to manufacture a large-area device. To solve this problem, a device using a solution process is being developed.

Therefore, development of materials for solution processing is required.

Korean Patent Publication No. 10-2012-0112277

It is an object of the present invention to provide novel compounds and/or ink compositions comprising them.

An object of the present invention is to provide an organic light emitting device comprising the aforementioned compound and/or the aforementioned ink composition.

An object of the present invention is to provide a method for manufacturing the organic light emitting device described above.

An exemplary embodiment of the present invention provides a compound represented by Formula 1 below.

[Formula 1]

In Formula 1,

X1 is a group represented by the following structural formula 1 or 2,

One of X2 and X3 is a group represented by the following structural formula 1 or 2, the other is hydrogen or deuterium,

If X1 is a group represented by Structural Formula 1 below, either X2 or X3 is a group represented by Structural Formula 2 below,

When X1 is a group represented by Structural Formula 2 below, either X2 or X3 is a group represented by Structural Formula 1 below,

[Structural Formula 1]

[Structural Formula 2]

In the structural formulas 1 and 2,

R11 and R12 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; A substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group,

L21 is a direct bond; Or a substituted or unsubstituted arylene group,

Y1 to Y3 are the same as or different from each other, each independently N or CRa, at least one of Y1 to Y3 is N,

Ra, R21 and R22 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; A substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group,

* means a position binding to Formula 1 above.

Another embodiment of the present invention provides an ink composition containing the compound.

An exemplary embodiment of the present invention also includes a first electrode; a second electrode; and one or more organic material layers provided between the first electrode and the second electrode, wherein at least one layer of the one or more organic material layers includes the aforementioned ink composition.

Finally, one embodiment of the present invention comprises preparing a first electrode; forming one or more organic material layers on the first electrode; and forming a second electrode on the one or more organic material layers, wherein the forming of the one or more organic material layers includes forming one or more organic material layers using the ink composition. A method for manufacturing a device is provided.

The compound represented by Chemical Formula 1 of the present invention can be used as a material for an organic layer of an organic light emitting device, and a device having low driving voltage, excellent efficiency characteristics and/or excellent lifetime characteristics can be obtained, and a solution process is possible, so that the device It is possible to enlarge the area.

1 illustrates an example of an organic light emitting device according to an exemplary embodiment of the present invention.

Hereinafter, the present invention will be described in detail.

An exemplary embodiment of the present invention provides a compound represented by Formula 1 below.

[Formula 1]

In Formula 1,

X1 is a group represented by the following structural formula 1 or 2,

One of X2 and X3 is a group represented by the following structural formula 1 or 2, the other is hydrogen or deuterium,

If X1 is a group represented by Structural Formula 1 below, either X2 or X3 is a group represented by Structural Formula 2 below,

When X1 is a group represented by Structural Formula 2 below, either X2 or X3 is a group represented by Structural Formula 1 below,

[Structural Formula 1]

[Structural Formula 2]

In the structural formulas 1 and 2,

R11 and R12 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; A substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group,

L21 is a direct bond; Or a substituted or unsubstituted arylene group,

Y1 to Y3 are the same as or different from each other, each independently N or CRa, at least one of Y1 to Y3 is N,

Ra, R21 and R22 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; A substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group,

* means a position binding to Formula 1 above.

Since the naphthalene derivative compound according to an exemplary embodiment of the present invention has an asymmetric structure, it is included in an organic light emitting device and has excellent driving voltage characteristics, efficiency characteristics, and/or lifetime characteristics. Specifically, in the compound represented by Formula 1, substituents are introduced to carbon 1 and carbon 6 of naphthalene, or substituents are introduced to carbon 1 and carbon 7 of naphthalene, so that each substituent is asymmetric around the naphthalene parent nucleus structure. introduced hostilely. Accordingly, the solubility of the molecule of the compound represented by Formula 1 increases. As a result, the organic light emitting device including the compound represented by Formula 1 has advantages such as low driving voltage, improved efficiency, and/or improved lifetime characteristics.

In addition, in the case of the compound according to an exemplary embodiment of the present invention, an organic light emitting device can be manufactured by a solution coating method, so that the device can have a large area.

In the present invention, when a member (layer) is said to be located "on" another member (layer), this means that a member (layer) is in contact with another member, as well as another member (layer) between two members (layer). The case where (layer) exists is also included.

In the present invention, when a part "includes" a certain component, it means that it may further include other components without excluding other components unless otherwise stated.

Hereinafter, the substituents of the present invention will be described in detail.

In the present invention, the term "substitution" means that a hydrogen atom bonded to a carbon atom of a compound is replaced with another substituent, and the position to be substituted is not limited as long as the hydrogen atom is substituted, that is, the position where the substituent can be substituted, When two or more substituents are substituted, two or more substituents may be the same as or different from each other.

In the present invention, the term "substituted or unsubstituted" is substituted or unsubstituted with one or more substituents selected from the group consisting of deuterium, halogen group, alkyl group, cycloalkyl group, aryl group and heteroaryl group, or two of the above exemplified substituents. It means that the above substituent is substituted or unsubstituted with a linked substituent. For example, "a substituent in which two or more substituents are connected" may be a biphenyl group. That is, the biphenyl group may be an aryl group, and may be interpreted as a substituent in which two phenyl groups are connected.

In addition, the term “substituted or unsubstituted” in the present invention includes heavy hydrogen, a halogen group, an alkyl group having 1 to 30 carbon atoms, a cycloalkyl group having 3 to 30 carbon atoms, an aryl group having 6 to 60 carbon atoms, and a heteroaryl group having 2 to 60 carbon atoms. It means substituted or unsubstituted with one or more substituents selected from the group consisting of groups, or substituted or unsubstituted with substituents in which two or more substituents among the above exemplified substituents are connected.

In the present invention, the halogen group is a fluoro group (-F), a chloro group (-Cl), a bromo group (-Br) or an iodo group (-I).

In the present invention, the alkyl group may be straight or branched, and the number of carbon atoms is not particularly limited, but may be 1 to 20. According to another exemplary embodiment, the number of carbon atoms of the alkyl group is 1 to 10. Specific examples of the alkyl group include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl, etc. , but not limited to these.

In the present invention, the cycloalkyl group is not particularly limited, but may have 3 to 60 carbon atoms, and according to an exemplary embodiment, the cycloalkyl group has 3 to 30 carbon atoms. According to another exemplary embodiment, the number of carbon atoms of the cycloalkyl group is 3 to 20. Specific examples of the cycloalkyl group include, but are not limited to, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, and a cyclooctyl group.

In the present invention, the aryl group is not particularly limited, but may have 6 to 60 carbon atoms, and may be a monocyclic aryl group or a polycyclic aryl group. According to one embodiment, the number of carbon atoms of the aryl group is 6 to 30. According to one embodiment, the number of carbon atoms of the aryl group is 6 to 20. The aryl group may be a phenyl group, a biphenyl group, a terphenyl group, etc. as a monocyclic aryl group, but is not limited thereto. The polycyclic aryl group may be a naphthyl group, anthracenyl group, phenanthrenyl group, pyrenyl group, perylenyl group, triphenylenyl group, chrysenyl group, fluorenyl group, and the like, but is not limited thereto.

In the present invention, the fluorenyl group may be substituted, and two substituents may be bonded to each other to form a spiro structure.

,

등의 스피로플루오레닐기,

(9,9-디메틸플루오레닐기), 및

(9,9-디페닐플루오레닐기) 등의 치환된 플루오레닐기가 될 수 있다. 다만, 이에 한정되는 것은 아니다.When the fluorenyl group is substituted,

,

spirofluorenyl groups such as;

(9,9-dimethylfluorenyl group), and

It may be a substituted fluorenyl group such as (9,9-diphenylfluorenyl group). However, it is not limited thereto.

In the present invention, the heteroaryl group is an aromatic ring group containing at least one of N, O, P, S, Si and Se as a heteroatom, and the number of carbon atoms is not particularly limited, but may have 2 to 60 carbon atoms. According to one embodiment, the carbon number of the heteroaryl group is 2 to 30. Examples of the heteroaryl group include a pyridine group, a pyrrole group, a pyrimidine group, a pyridazine group, a furan group, a thiophene group, a benzothiophene group, a benzofuran group, a dibenzothiophene group, a dibenzofuran group, and the like. However, it is not limited to these.

In the present invention, the above description of the aryl group is applied except that the arylene group is divalent.

According to an exemplary embodiment of the present invention, Formula 1 is represented by Formulas 11 to 14 below.

[Formula 11]

[Formula 12]

[Formula 13]

[Formula 14]

In Formulas 11 to 14,

R11, R12, L21, Y1 to Y3, R21 and R22 are as defined in Formula 1 above.

According to an exemplary embodiment of the present invention, R11 and R12 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; A substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group.

According to an exemplary embodiment of the present invention, R11 and R12 are the same as or different from each other, and each independently a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms; or a substituted or unsubstituted aryl group having 6 to 30 carbon atoms.

According to an exemplary embodiment of the present invention, R11 and R12 are the same as or different from each other, and each independently a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms; or a substituted or unsubstituted aryl group having 6 to 20 carbon atoms.

According to an exemplary embodiment of the present invention, R11 and R12 are the same as or different from each other, and each independently a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms; or a substituted or unsubstituted aryl group having 6 to 12 carbon atoms.

According to an exemplary embodiment of the present invention, R11 and R12 are the same as or different from each other, and each independently a substituted or unsubstituted methyl group; Or a substituted or unsubstituted phenyl group.

According to an exemplary embodiment of the present invention, R11 and R12 are the same as or different from each other, and each independently represents a methyl group or a phenyl group.

According to an exemplary embodiment of the present invention, L21 is a direct bond; Or a substituted or unsubstituted arylene group.

According to an exemplary embodiment of the present invention, L21 is a direct bond; or a substituted or unsubstituted arylene group having 6 to 30 carbon atoms.

According to an exemplary embodiment of the present invention, L21 is a direct bond; or a substituted or unsubstituted arylene group having 6 to 20 carbon atoms.

According to an exemplary embodiment of the present invention, L21 is a direct bond; or a substituted or unsubstituted arylene group having 6 to 12 carbon atoms.

According to an exemplary embodiment of the present invention, L21 is a direct bond; Or a substituted or unsubstituted phenylene group.

According to an exemplary embodiment of the present invention, L21 is a direct bond or a phenylene group.

According to an exemplary embodiment of the present invention, Y1 to Y3 are the same as or different from each other, each independently represent N or CRa, and at least one of Y1 to Y3 is N.

According to an exemplary embodiment of the present invention, any two of Y1 to Y3 are N, and the other is CRa.

According to an exemplary embodiment of the present invention, Y1 to Y3 are N.

According to an exemplary embodiment of the present invention, R21 and R22 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; A substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group.

According to an exemplary embodiment of the present invention, R21 and R22 are the same as or different from each other, and each independently a substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group.

According to an exemplary embodiment of the present invention, R21 and R22 are the same as or different from each other, and each independently represents a substituted or unsubstituted aryl group having 6 to 30 carbon atoms.

According to an exemplary embodiment of the present invention, R21 and R22 are the same as or different from each other, and each independently represents a substituted or unsubstituted aryl group having 6 to 20 carbon atoms.

According to an exemplary embodiment of the present invention, R21 and R22 are the same as or different from each other, and each independently represents a substituted or unsubstituted aryl group having 6 to 12 carbon atoms.

According to an exemplary embodiment of the present invention, R21 and R22 are the same as or different from each other, and each independently a phenyl group unsubstituted or substituted with an alkyl group; Or a substituted or unsubstituted biphenyl group.

According to an exemplary embodiment of the present invention, R21 and R22 are the same as or different from each other, and each independently a phenyl group unsubstituted or substituted with an alkyl group; or a biphenyl group.

According to an exemplary embodiment of the present invention, R21 and R22 are the same as or different from each other, and each independently a phenyl group unsubstituted or substituted with a tertbutyl group; or a biphenyl group.

According to an exemplary embodiment of the present invention, the compound represented by Formula 1 is any one selected from the group consisting of the following compounds.

.

.

The compound represented by Formula 1 according to an exemplary embodiment of the present invention is a palladium-catalyzed coupling reaction of naphthalene and phosphine oxide; Alternatively, they may be combined by a method known in the art, such as a palladium-catalyzed coupling reaction of naphthalene and triazine, and the type, position or number of substituents may be changed according to techniques known in the art.

Hereinafter, an ink composition including the aforementioned compound will be described in detail.

According to an exemplary embodiment of the present invention, the ink composition includes the compound represented by Chemical Formula 1 and a solvent.

According to an exemplary embodiment of the present invention, the ink composition may be in liquid form.

According to an exemplary embodiment of the present invention, the solvent is, for example, a chlorine-based solvent such as chloroform, methylene chloride, 1,2-dichloroethane, 1,1,2-trichloroethane, chlorobenzene, o-dichlorobenzene; ether solvents such as tetrahydrofuran and dioxane; aromatic hydrocarbon solvents such as toluene, xylene, trimethylbenzene, and mesitylene; aliphatic hydrocarbon-based solvents such as cyclohexane, methylcyclohexane, n-pentane, n-hexane, n-heptane, n-octane, n-nonane, and n-decane; ketone-based solvents such as acetone, methyl ethyl ketone, cyclohexanone, isophorone, tetralone, decalone, and acetylacetone; Ester solvents, such as ethyl acetate, butyl acetate, and ethyl cellosolve acetate; Ethylene glycol, ethylene glycol monobutyl ether, ethylene glycol monoethyl ether, ethylene glycol monomethyl ether, dimethoxyethane, propylene glycol, diethoxymethane, triethylene glycol monoethyl ether, glycerin, 1,2-hexanediol, etc. alcohol and its derivatives; alcohol solvents such as methanol, ethanol, propanol, isopropanol, and cyclohexanol; sulfoxide-based solvents such as dimethyl sulfoxide; and amide solvents such as N-methyl-2-pyrrolidone and N,N-dimethylformamide; Solvents such as tetralin are exemplified, but any solvent capable of dissolving or dispersing the compound represented by Formula 1 according to an exemplary embodiment of the present invention is sufficient, but is not limited thereto.

According to an exemplary embodiment of the present invention, the solvent may be used alone or in combination of two or more solvents.

According to an exemplary embodiment of the present invention, the ink composition may include an electron injection layer dopant material; an electron transport layer dopant material; Alternatively, an electron injection and transport layer may further include a dopant material. the electron injection layer dopant material; an electron transport layer dopant material; Alternatively, the electron injection and transport layer dopant material may include at least one selected from the group consisting of organic-inorganic mixtures, metals, and organic salts.

According to an exemplary embodiment of the present invention, the electron injection layer dopant material; an electron transport layer dopant material; Alternatively, the electron injection and transport layer dopant material may be an organic material including a substituent including CN and/or F.

According to an exemplary embodiment of the present invention, the electron injection layer dopant material; an electron transport layer dopant material; Alternatively, the electron injection and transport layer dopant material may include one or more selected from the group consisting of alkali metals, alkaline earth metals, lanthanide metals, Se, Ru, and compounds thereof. Specifically, the alkali metal may be Li. Also, the alkaline earth metal may be Ca and Mg. Also, the compound may be LiF, Liq, and RuCO ₃ . In addition, the lanthanide metal may be Yb.

According to an exemplary embodiment of the present invention, the electron injection layer dopant material; an electron transport layer dopant material; Alternatively, the electron injection and transport layer dopant material may include fullerene. Specifically, the fullerene may be fullerene having 60 carbon atoms or fullerene having 70 carbon atoms.

According to an exemplary embodiment of the present invention, the electron injection layer dopant material; an electron transport layer dopant material; Alternatively, the electron injection and transport layer dopant material may include a halide. Specifically, the halogenated flame may be LiF.

According to an exemplary embodiment of the present invention, the electron injection layer dopant material; an electron transport layer dopant material; or the content of the electron injection and transport layer dopant material is the electron injection layer dopant material; an electron transport layer dopant material; Alternatively, it may be 1% by weight or more and 50% by weight or less based on the total weight of the layer including the electron injection and transport layer dopant material.

According to another exemplary embodiment of the present invention, the ink composition may include a single molecule including a photocurable group and/or a thermosetting group; Or, it further includes a single molecule including an end group capable of forming a polymer by heat. As described above, a single molecule containing a photocurable group and/or a thermosetting group; Alternatively, the molecular weight of a single molecule including an end group capable of forming a polymer by heat may be a compound of 3,000 g/mol or less, but is not limited to the above-exemplified molecular weight.

a single molecule containing the photocurable group and/or thermocurable group; Alternatively, a single molecule including an end group capable of forming a polymer by heat may be aryl such as phenyl, biphenyl, fluorene, or naphthalene; arylamine; Alternatively, it may refer to a single molecule in which fluorene is substituted with a photocurable group and/or a thermosetting group or a terminal group capable of forming a polymer by heat.

According to an exemplary embodiment of the present invention, the ink composition has a viscosity of 2 cP to 15 cP at room temperature. When the above viscosity is satisfied, it is easy to manufacture a device. Specifically, when forming the organic material layer in the organic light emitting device, a uniform film may be formed.

An exemplary embodiment of the present invention is a compound represented by Formula 1; Alternatively, an organic light emitting device including an ink composition including the compound represented by Chemical Formula 1 is provided.

An exemplary embodiment of the present invention provides an organic light emitting device formed using the ink composition.

An exemplary embodiment of the present invention is a first electrode; a second electrode; and one or more organic material layers provided between the first electrode and the second electrode, wherein at least one layer of the one or more organic material layers includes the ink composition described above.

Hereinafter, types of organic material layers included in the organic light emitting device described above will be described in detail.

According to an exemplary embodiment of the present invention, the organic light emitting device includes one organic material layer, and the organic material layer includes the compound represented by Chemical Formula 1. As an example, the organic material layer including the compound represented by Chemical Formula 1 is a light emitting layer.

According to another exemplary embodiment of the present invention, the organic light emitting device includes two or more organic material layers, and the two or more organic material layers include the compound represented by Chemical Formula 1. For example, any one organic material layer among the two or more organic material layers includes the compound represented by Chemical Formula 1, and further includes one or more other organic material layers. According to an exemplary embodiment, the remaining one or more organic material layers do not include the compound represented by Chemical Formula 1. According to another exemplary embodiment, the remaining one or more organic material layers further include the compound represented by Chemical Formula 1. However, it is not limited to the above example.

The two or more organic material layers are selected from the group consisting of, for example, a hole injection layer, a hole transport layer, a hole injection and transport layer, an electron blocking layer, a light emitting layer, a hole blocking layer, an electron transport layer, an electron injection layer, an electron injection and transport layer, and the like Contains two or more layers. In this case, the hole injection and transport layer means a layer that simultaneously injects holes and transports holes, and the electron injection and transport layer means a layer that simultaneously injects and transports electrons. However, the organic material layer constituting the group is only an example, and is not limited to the example. In addition, the two or more organic material layers may include two or more layers performing the same role as necessary. An organic light emitting device according to an example includes a first electron transport layer and a second electron transport layer. However, it is not limited to the above example.

According to one embodiment of the present invention, the organic material layer includes a light emitting layer. As an example, the light emitting layer includes the compound represented by Chemical Formula 1. As a specific example, the light emitting layer includes the compound represented by Chemical Formula 1 as a host of the light emitting layer. As another specific example, the light emitting layer includes the compound represented by Chemical Formula 1 as a dopant of the light emitting layer.

According to an exemplary embodiment of the present invention, the organic material layer includes an electron injection and transport layer, an electron injection layer or an electron transport layer. As an example, the electron injection and transport layer, the electron injection layer or the electron transport layer includes the compound represented by Chemical Formula 1.

According to an exemplary embodiment of the present invention, the organic material layer includes an electron transport layer. As an example, the electron transport layer includes the compound represented by Chemical Formula 1.

According to an exemplary embodiment of the present invention, the organic material layer further includes one or more layers selected from the group consisting of an electron blocking layer, a hole blocking layer, a hole injection layer, a hole transport layer, and a hole injection and transport layer. As an example, one or more layers selected from the group consisting of the electron blocking layer, the hole blocking layer, the hole injection layer, the hole transport layer, and the hole injection and transport layer are a compound represented by Formula 1 or a compound containing the same. It contains an ink composition.

According to an exemplary embodiment of the present invention, the one or more organic material layers include the light emitting layer and the one or more first organic material layers, and at least one of the one or more first organic material layers includes the ink composition described above. In this case, when the one or more first organic material layers are two or more layers, the two or more first organic material layers are the same as or different from each other.

Hereinafter, a laminated structure of the organic material layer and the organic light emitting device including the same will be described in detail.

An organic material layer of an organic light emitting device according to an exemplary embodiment of the present invention has a single-layer structure. For example, the single-layer organic material layer is provided between the first electrode and the second electrode of the organic light emitting device, and the organic material layer includes the compound represented by Chemical Formula 1. According to a specific embodiment, the organic material layer having a single-layer structure is a light emitting layer, and in this case, the light emitting layer includes the compound represented by Chemical Formula 1.

An organic material layer of an organic light emitting device according to another exemplary embodiment of the present invention has a multilayer structure in which two or more organic material layers are stacked. For example, the organic material layer of the multilayer structure is provided between the first electrode and the second electrode of the organic light emitting device.

According to an exemplary embodiment of the present invention, the organic material layer of the multi-layered structure includes a light emitting layer and organic material layers other than the light emitting layer. As an example, the light emitting layer is provided between the first electrode and the second electrode, and an organic material layer other than the light emitting layer is provided between the first electrode and the light emitting layer. As another example, the light emitting layer is provided between the first electrode and the second electrode, and an organic material layer other than the light emitting layer is provided between the light emitting layer and the second electrode. As another example, the light emitting layer is provided between the first electrode and the second electrode, any one organic material layer other than the light emitting layer is provided between the first electrode and the light emitting layer, and any other organic material layer other than the light emitting layer is It is provided between the light emitting layer and the second electrode. However, the above structure is only an example, and is not limited to the above structure. In addition, the organic material layer other than the light emitting layer is selected from the group consisting of, for example, a hole injection and transport layer, a hole injection layer, a hole transport layer, an electron blocking layer, a hole blocking layer, an electron transport layer, an electron injection layer, an electron injection and transport layer, and the like It may be one or more layers, but is not limited thereto.

In general, in an organic light emitting device, a hole injection layer, a hole transport layer, or an electron blocking layer is provided between the anode and the light emitting layer. As a specific example, the hole injection layer is provided over the anode, the hole transport layer is provided over the hole injection layer, and the electron blocking layer is provided over the hole injection layer, but is not limited to the above examples.

Also, in general, an electron injection layer, an electron transport layer, or a hole blocking layer is provided between the cathode and the light emitting layer in an organic light emitting device. As a specific example, the hole blocking layer is provided on the light emitting layer, the electron transport layer is provided on the hole blocking layer, and the electron injection layer is provided on the electron transport layer, but is not limited to the above example.

An organic material layer having a multilayer structure included in an organic light emitting device according to an exemplary embodiment of the present invention includes a light emitting layer; and one or more first organic material layers selected from the group consisting of a hole injection and transport layer, a hole injection layer, a hole transport layer, an electron blocking layer, a hole blocking layer, an electron transport layer, an electron injection layer, and an electron injection and transport layer, wherein the light emitting layer Silver is provided between the first electrode and the second electrode, and the one or more first organic material layers are provided between the light emitting layer and the second electrode. As an example, the one or more first organic material layers include the compound represented by Chemical Formula 1.

According to a preferred embodiment of the present invention, the one or more first organic material layers include an electron injection layer; electron transport layer; and at least one of an electron injection and transport layer. More preferably, the at least one first organic material layer is an electron transport layer.

A structure of an organic light emitting device according to an exemplary embodiment of the present invention is shown in FIG. 1 . 1 shows a first electrode 201, a hole injection layer 301, a hole transport layer 401, a light emitting layer 501, an electron transport layer 601, an electron injection layer 701, and a second electrode on a substrate 101. A structure of an organic light emitting device in which 801 is sequentially stacked is illustrated. The electron injection and transport layer 601 of FIG. 1 may include a compound represented by Chemical Formula 1; Alternatively, it may include an ink composition including the compound represented by Formula 1, or may be formed using the ink composition. 1 illustrates an organic light emitting device according to an exemplary embodiment of the present invention, but is not limited thereto.

According to an exemplary embodiment of the present invention, the first electrode is an anode and the second electrode is a cathode.

According to another exemplary embodiment of the present invention, the first electrode is a cathode, and the second electrode is an anode.

As described above, the organic light emitting device having a single-layer or multi-layered organic material layer may have, for example, a laminated structure as described below, but is not limited thereto.

(1) anode/hole transport layer/light emitting layer/cathode

(2) anode/hole injection layer/hole transport layer/light emitting layer/cathode

(3) anode/hole injection layer/hole buffer layer/hole transport layer/light emitting layer/cathode

(4) anode/hole transport layer/light emitting layer/electron transport layer/cathode

(5) anode/hole transport layer/light emitting layer/electron transport layer/electron injection layer/cathode

(6) anode/hole injection layer/hole transport layer/light emitting layer/electron transport layer/cathode

(7) anode/hole injection layer/hole transport layer/light emitting layer/electron transport layer/electron injection layer/cathode

(8) anode/hole injection layer/hole buffer layer/hole transport layer/light emitting layer/electron transport layer/cathode

(9) anode/hole injection layer/hole buffer layer/hole transport layer/light emitting layer/electron transport layer/electron injection layer/cathode

(10) anode/hole transport layer/electron blocking layer/emission layer/electron transport layer/cathode

(11) anode/hole transport layer/electron blocking layer/emission layer/electron transport layer/electron injection layer/cathode

(12) anode / hole injection layer / hole transport layer / electron blocking layer / light emitting layer / electron transport layer / cathode

(13) anode / hole injection layer / hole transport layer / electron blocking layer / light emitting layer / electron transport layer / electron injection layer / cathode

(14) anode/hole transport layer/light emitting layer/hole blocking layer/electron transport layer/cathode

(15) anode/hole transport layer/light emitting layer/hole blocking layer/electron transport layer/electron injection layer/cathode

(16) anode/hole injection layer/hole transport layer/light emitting layer/hole blocking layer/electron transport layer/cathode

(17) anode/hole injection layer/hole transport layer/light emitting layer/hole blocking layer/electron transport layer/electron injection layer/cathode

(18) anode/hole injection layer/hole transport layer/light emitting layer/hole blocking layer/electron transport layer/electron injection layer/cathode/capsule

(19) anode/hole injection layer/first hole transport layer/second hole transport layer/light emitting layer/hole blocking layer/electron transport layer/electron injection layer/cathode/capsule

According to an exemplary embodiment of the present invention, the organic light emitting device may be a normal type organic light emitting device in which an anode, one or more organic material layers, and a cathode are sequentially stacked on a substrate.

According to another exemplary embodiment of the present invention, the organic light emitting device may be an inverted type organic light emitting device in which a cathode, one or more organic material layers, and an anode are sequentially stacked on a substrate.

Hereinafter, specific details of the organic material layer described above, materials thereof, and manufacturing methods thereof will be described. However, the organic light emitting diode of the present invention may be manufactured with materials and methods known in the art, except that the organic material layer includes the above compounds.

An organic light emitting device according to an exemplary embodiment of the present invention is formed by using an ink composition containing the compound represented by Chemical Formula 1 above at least one of the organic material layers. Except for this, it can be manufactured with materials and methods known in the art.

For example, the organic light emitting device of the present invention can be manufactured by sequentially stacking an anode, an organic material layer, and a cathode on a substrate. At this time, using a PVD (Physical Vapor Deposition) method such as sputtering or e-beam evaporation, depositing a metal or a metal oxide having conductivity or an alloy thereof on the substrate to form an anode, After forming an organic material layer including at least one layer of a hole injection layer, a hole transport layer, a light emitting layer, an electron injection layer, an electron transport layer, a hole transport and injection layer, and an electron transport and injection layer thereon through a solution process, a deposition process, etc. It can be manufactured by depositing a material that can be used as a cathode thereon. In addition to this method, an organic light emitting device may be manufactured by sequentially depositing a cathode material, an organic material layer, and an anode material on a substrate.

An exemplary embodiment of the present invention also provides a method of manufacturing an organic light emitting device formed using the ink composition.

Specifically, according to an exemplary embodiment of the present invention, preparing a first electrode; forming one or more organic material layers on the first electrode; and forming a second electrode on the one or more organic material layers, wherein the forming of the one or more organic material layers includes forming the organic material layer using the ink composition described above.

According to an exemplary embodiment of the present invention, the step of forming one or more organic material layers using the ink composition uses a spin coating method.

According to another exemplary embodiment of the present invention, the step of forming one or more organic material layers using the ink composition uses a printing method.

According to an exemplary embodiment of the present invention, the printing method includes, for example, inkjet printing, nozzle printing, offset printing, transfer printing, or screen printing, but is not limited to the above-listed printing methods.

Since the ink composition according to an exemplary embodiment of the present invention is suitable for a solution process due to structural characteristics and can be formed by a printing method, there is an economical effect in terms of time and cost when manufacturing a device.

According to an exemplary embodiment of the present invention, the forming of one or more organic material layers using the ink composition may include coating the ink composition; and drying the coated ink composition; heat treatment step; and/or a light treatment step.

According to an exemplary embodiment of the present invention, the forming of one or more organic material layers using the ink composition may include coating an ink composition on the first electrode or the one or more organic material layers; and drying the coated ink composition; heat treatment step; and/or a light treatment step. Preferably, the forming of one or more organic material layers using the ink composition may include coating an ink composition on the one or more organic material layers; and drying or heat-treating the coated ink composition. As an example, the forming of one or more organic material layers using the ink composition may include coating an ink composition on the first electrode or the one or more organic material layers; and drying the coated ink composition. As another example, the forming of one or more organic material layers using the ink composition may include coating an ink composition on the first electrode or the one or more organic material layers; and heat-treating the coated ink composition. More preferably, the forming of one or more organic material layers using the ink composition may include coating an ink composition on the one or more organic material layers; and drying and heat-treating the coated ink composition.

According to one embodiment of the present invention, the heat treatment step may be performed through heat treatment, and the heat treatment temperature in the heat treatment step may be 85 ° C to 250 ° C, and according to one embodiment, 100 ° C to 250 ° C, In another exemplary embodiment, it may be 150 ℃ to 250 ℃.

According to one embodiment of the present invention, the heat treatment time in the heat treatment step is 1 minute to 2 hours, according to one embodiment it may be 1 minute to 1 hour, and in another embodiment, 10 minutes to 1 hour. As a preferred example, the heat treatment time in the heat treatment step is 20 minutes to 40 minutes.

In the step of forming one or more organic material layers formed using the ink composition, including the heat treatment or light treatment step, the ink composition includes a photocurable group and/or a single molecule including a thermosetting group; Alternatively, when a single molecule including a terminal group capable of forming a polymer by heat is further included, cross-linking between components included in the ink composition may be formed to provide an organic layer having a thinned structure. In this case, when another layer is laminated on the surface of the organic layer formed using the ink composition, it is possible to prevent it from being dissolved by a solvent, morphologically affected, or decomposed. Therefore, when the organic material layer is formed according to the above manufacturing method, resistance to solvent is increased, so that a multi-layer may be formed by repeatedly performing solution deposition and crosslinking methods, and stability may be increased, thereby increasing lifespan characteristics of the device.

Hereinafter, materials for the above-described anode, cathode, and specific organic layer will be described in detail.

As the anode material, a material having a high work function is generally preferred so that holes can be smoothly injected into the organic material layer. For example, metals such as vanadium, chromium, copper, zinc, gold or alloys thereof; metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO); ZnO:Al or SnO ₂ : A combination of a metal and an oxide such as Sb; Conductive polymers such as poly(3-methylthiophene), poly[3,4-(ethylene-1,2-dioxy)thiophene] (PEDOT), polypyrrole, and polyaniline, but are not limited thereto.

The cathode material is preferably a material having a small work function so as to facilitate electron injection into the organic material layer. For example, metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin and lead or alloys thereof; There are multi-layered materials such as LiF/Al or LiO ₂ /Al, but are not limited thereto.

The light emitting layer may include a host material and/or a dopant material.

Examples of the host material include a condensed aromatic ring derivative or a heterocyclic compound. Specifically, condensed aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, and fluoranthene compounds, and heterocyclic-containing compounds include dibenzofuran derivatives, ladder-type furan compounds, pyrimidine derivatives and the like, but are not limited thereto.

According to one embodiment of the present invention, as the host material, two or more host materials selected from among the above-described host materials may be mixed and used. For example, an anthracene derivative and a pyrene derivative may be mixed and used in a weight ratio of 1:99 to 99:1. As a more specific example, an anthracene derivative and a pyrene derivative may be mixed and used in a weight ratio of 92:8.

Examples of the dopant material include an aromatic amine derivative, a strylamine compound, a boron complex, a fluoranthene compound, and a metal complex. Specifically, aromatic amine derivatives include pyrene, anthracene, chrysene, and periplanthene having an arylamine group as condensed aromatic ring derivatives having a substituted or unsubstituted arylamine group. In addition, the styrylamine compound is a compound in which at least one arylvinyl group is substituted for a substituted or unsubstituted arylamine, and one or two or more are selected from the group consisting of an aryl group, a silyl group, an alkyl group, a cycloalkyl group, and an arylamine group. The substituent is substituted or unsubstituted. Specifically, there are styrylamine, styryldiamine, styryltriamine, styryltetraamine, etc., but is not limited thereto. In addition, metal complexes include, but are not limited to, iridium complexes and platinum complexes.

The hole injection layer is a layer that receives holes from an electrode. It is preferable that the hole injecting material has the ability to transport holes and has a hole receiving effect from the anode and an excellent hole injecting effect with respect to the light emitting layer or the light emitting material. In addition, a material having excellent ability to prevent movement of excitons generated in the light emitting layer to the electron injection layer or electron injection material is desirable. Also, a material having excellent thin film forming ability is preferred. In addition, it is preferable that the HOMO of the hole injection material is between the work function of the anode material and the HOMO of the surrounding organic material layer. Specific examples of the hole injection material include metal porphyrins, oligothiophenes, and arylamine-based organic materials; hexanitrile hexaazatriphenylene-based organic materials; quinacridone-based organic substances; perylene-based organic materials; Examples include polythiophene-based conductive polymers such as anthraquinone and polyaniline, but are not limited thereto.

The hole transport layer is a layer that receives holes from the hole injection layer and transports the holes to the light emitting layer, and may have a single layer or a multilayer structure of two or more layers. The hole transport material is a material capable of receiving holes from the anode or the hole injection layer and transporting them to the light emitting layer, and a material having high hole mobility is preferable.

The electron transport layer is a layer that receives electrons from the electron injection layer and transports the electrons to the light emitting layer. The electron transport material is a material capable of receiving electrons from the cathode and transferring them to the light emitting layer, and a material having high electron mobility is preferable. Specific examples 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 transport layer can be used with any desired cathode material, as used according to the prior art. In particular, a suitable cathode material is a conventional material having a low work function, followed by a layer of aluminum or silver. Specifically, there are cesium, barium, calcium, ytterbium and samarium, etc., followed by an aluminum layer or a silver layer in each case.

The electron injection layer is a layer that receives electrons from an electrode. As the electron injecting material, it is preferable to have an excellent ability to transport electrons, an electron receiving effect from the cathode, and an excellent electron injecting effect with respect to the light emitting layer or the light emitting material. In addition, a material that prevents excitons generated in the light emitting layer from moving to the hole injection layer and has excellent thin film forming ability is preferred. Specifically, fluorenone, anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, preorenylidene methane, anthrone, etc. and their derivatives, metal complex compounds and nitrogen-containing 5-membered ring derivatives, but are not limited thereto. Examples of the metal complex compound include 8-hydroxyquinolinato lithium, bis(8-hydroxyquinolinato)zinc, bis(8-hydroxyquinolinato)copper, and bis(8-hydroxyquinolinato)manganese. , tris (8-hydroxyquinolinato) aluminum, tris (2-methyl-8-hydroxyquinolinato) aluminum, tris (8-hydroxyquinolinato) gallium, bis (10-hydroxybenzo [h ]quinolinato) beryllium, bis(10-hydroxybenzo[h]quinolinato)zinc, bis(2-methyl-8-quinolinato)chlorogallium, bis(2-methyl-8-quinolinato) (o-cresolato)gallium, bis(2-methyl-8-quinolinato)(1-naphtolato)aluminum, bis(2-methyl-8-quinolinato)(2-naphtolato)gallium, etc. , but is not limited thereto. According to a preferred embodiment of the present invention, the electron transport material is a compound represented by the above formula (1).

The electron blocking layer is a layer capable of improving lifespan or efficiency of a device by preventing electrons injected from the electron injection layer from passing through the light emitting layer and entering the hole injection layer. A known electron blocking material may be used as the electron blocking material.

The hole blocking layer is a layer that blocks holes from reaching the cathode, and may be generally formed under the same conditions as the electron injection layer. Specific examples of the hole blocking layer material include oxadiazole derivatives, triazole derivatives, phenanthroline derivatives, and aluminum complexes, but are not limited thereto.

The hole injection and transport layer may include the above-described hole injection and hole transport layer materials.

The electron injection and transport layer may include materials for the electron injection and hole transport layers described above.

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

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

An exemplary embodiment of the present invention is a compound represented by Formula 1; Alternatively, an electronic device including an organic light emitting device including an ink composition including the compound represented by Chemical Formula 1 or an organic material layer formed using the ink composition is provided.

The electronic device is an interlayer insulating film of a semiconductor device, a color filter, a black matrix, an overcoat, a column spacer, a passivation film, a buffer coat film, an insulating film for a multilayer printed circuit board, a cover coat of a flexible copper clad plate, a buffer coat film, and a multilayer printed circuit board Insulation film solder resist film, OLED insulation film, thin film transistor protective film of liquid crystal display device, electrode protective film and semiconductor protective film of organic EL element, OLED insulating film, LCD insulating film, semiconductor insulating film, solar module, touch panel, display panel, etc. It may include all devices and the like, but is not limited thereto.

Hereinafter, examples will be described in detail to explain the present invention in detail. However, embodiments according to the present invention can be modified in many different forms, and the scope of the present invention is not construed as being limited to the embodiments described below. Embodiments of the present invention are provided to more completely explain the present invention to those skilled in the art.

<Production Example>

Preparation Example 1. Preparation of Compound 1

(Production Example 1-1)

Intermediate 1a, Intermediate 1b (1.0 equiv.), Cesium carbonate (2.5 equiv.), 1,1'-bis (diphenylphosphino) ferrocene [1,1'-Bis (diphenylphosphino) ferrocene] (0.1 equiv.) After putting it in a round bottom flask and filling it with nitrogen, dioxane (0.2 M) was added. Subsequently, palladium acetate (0.05 equiv.) was added, and the mixture was stirred under reflux overnight at 100°C. After the reaction was terminated by adding distilled water, the organic layer was extracted with dichloromethane/water, stirred for 30 minutes with anhydrous magnesium sulfate and activated carbon, and then passed through a diatomaceous earth/silica pad. After concentration under reduced pressure, column purification (ethyl acetate/hexane) gave intermediate 1c.

(Production Example 1-2)

The obtained intermediate 1c was placed in a round bottom flask, filled with nitrogen, and pyridine (2.0 equiv.) and dichloromethane (0.15 M) were added thereto. After confirming the dissolution, the temperature was lowered to 0° C. and trifluoromethanesulfonic acid anhydride [triflic anhydride] (1.2 equiv.) was slowly added dropwise. After stirring at room temperature for 6 hours, distilled water was added to terminate the reaction, the organic layer was extracted, anhydrous magnesium sulfate was added, stirred for 30 minutes, and passed through a celite/silica pad. After concentration under reduced pressure, precipitation with tetrahydrofuran/ethanol gave intermediate 1d.

(Production Example 1-3)

The resulting intermediate 1d, intermediate 1e (1.0 equiv.), and potassium carbonate (2.5 equiv.) were placed in a round bottom flask, filled with nitrogen, and tetrahydrofuran (0.2 M) and distilled water (0.05 M) were added to dissolve them. Subsequently, Pd(PPh ₃ ) ₄ (0.05 equiv.) was added and the mixture was refluxed and stirred overnight at 80°C. After the reaction was terminated by adding distilled water, the organic layer was extracted with dichloromethane/water, stirred for 30 minutes with anhydrous magnesium sulfate and activated carbon, and then passed through a diatomaceous earth/silica pad. After concentration under reduced pressure, compound 1 was obtained by precipitation with tetrahydrofuran/ethanol.

MS: [M+H] ⁺ = 636

Preparation Example 2. Preparation of Compound 2

Compound 2 was prepared in the same manner as in Preparation Example 1, except that 2a was used instead of 1e in Preparation Example 1-3.

MS: [M+H] ⁺ = 748

Preparation Example 3. Preparation of Compound 3

Intermediates 3b, 3c and Compound 3 were prepared in the same manner as in Preparation Example 1, except that 3a instead of 1a in Preparation Example 1-1 and 3d instead of 1e in Preparation Example 1-3 were used.

MS: [M+H] ⁺ = 636

Preparation Example 4. Preparation of Compound 4

Compound 4 was prepared in the same manner as in Preparation Example 3, except that 4a was used instead of 3d in Preparation Example 3.

MS: [M+H] ⁺ = 768

Preparation Example 5. Preparation of Compound 5

Intermediates 5b, 5c and Compound 5 were prepared in the same manner as in Preparation Example 1, except that 5a instead of 1a in Preparation Example 1-1 and 2a instead of 1e in Preparation Example 1-3 were used.

MS: [M+H] ⁺ = 748

<Device example>

Example 1. Manufacturing of organic light emitting device

A glass substrate on which indium tin oxide (ITO) was deposited with a thickness of 500 Å was placed in distilled water in which detergent was dissolved and washed with ultrasonic waves. At this time, a Fisher Co. product was used as a detergent, and distilled water filtered through a filter of a Millipore Co. product was used as distilled water. After washing the ITO for 30 minutes, ultrasonic cleaning was performed twice with distilled water for 10 minutes. After washing with distilled water, ultrasonic cleaning was performed with acetone, distilled water, and isopropyl alcohol solvent, and drying was performed to prepare a cleaned ITO glass substrate.

On the ITO transparent electrode, a composition obtained by mixing the following compound Z-1 and the following compound Z-2 at a weight ratio of 8:2 was spin-coated and cured on a hot plate under a nitrogen atmosphere at 220 ° C. for 30 minutes to obtain a 400 Å thick A hole injection layer was formed. On the hole injection layer, a composition obtained by dissolving the following compound Z-3 in toluene at a weight ratio of 1% was spin-coated and heat-treated on a hot plate at 200° C. for 30 minutes to form a hole transport layer having a thickness of 200 Å. On the hole transport layer, a composition obtained by dissolving the following compound Z-4 and the following compound Z-5 in a weight ratio of 98:2 in toluene at a weight ratio of 0.5% was spin-coated to form a light emitting layer having a thickness of 400 Å, and on a hot plate under a nitrogen atmosphere. The coating composition was dried under conditions of 120° C. and 10 minutes.

On the light emitting layer, compound 1 prepared in Preparation Example 1 and lithium quinolate (LiQ) were dissolved at a weight ratio of 3:7 in a mixed solvent of ethylene glycol and 1-propanol (volume ratio of 8:2) at a weight ratio of 1%. The coating composition was spin-coated and heat-treated at 145° C. for 10 minutes to form an electron injection and transport layer with a thickness of 300 Å.

A cathode was formed by depositing aluminum to a thickness of 1000 Å on the electron injection and transport layer. The deposition rate was maintained at 2 Å/s, and the degree of vacuum was maintained at 2*10 ^-7 to 5*10 ^-8 torr.

Examples 2 to 5

An organic light emitting device was manufactured in the same manner as in Example 1, except that the compound shown in Table 1 was used instead of Compound 1 when preparing the electron injection and transport layer.

Comparative Examples 1 and 2

An organic light-emitting device was manufactured in the same manner as in Example 1, except that Compound A or B was used in the preparation of the electron injection and transport layer, as shown in Table 1 below instead of Compound 1.

Table 1 below shows the results of measuring driving voltage, luminous efficiency, external quantum efficiency, and lifetime of the organic light emitting devices prepared in Examples and Comparative Examples at a current density of 10 mA/cm ² . T95 means the time (hr) required for the luminance to decrease from the initial luminance (1000 nit) to 95%.

electron injection and transport materials drive voltage
(V) luminous efficiency
(cd/A) quantum efficiency
(%) T95
(hr) Example 1 compound 1 4.93 5.51 5.87 135 Example 2 compound 2 4.82 5.32 5.68 122 Example 3 compound 3 4.88 5.19 5.70 111 Example 4 compound 4 4.95 5.50 5.98 104 Example 5 compound 5 4.77 5.53 5.79 131 Comparative Example 1 compound A 5.51 4.56 4.99 42 Comparative Example 2 compound B 6.08 4.15 4.90 23

As shown in Table 1, it can be confirmed that the organic light emitting device using the compound represented by Formula 1 according to the present invention as an electron injection and transport material has a significantly reduced driving voltage and greatly improved efficiency and lifetime characteristics compared to the comparative example. could

101: substrate
201: first electrode
301: hole injection layer
401: hole transport layer
501: light emitting layer
601: electron injection and transport layer
701: second electrode

Claims (14)

A compound represented by Formula 1 below:
[Formula 1]

In Formula 1,
X1 is a group represented by the following structural formula 1 or 2,
One of X2 and X3 is a group represented by the following structural formula 1 or 2, the other is hydrogen or deuterium,
If X1 is a group represented by Structural Formula 1 below, either X2 or X3 is a group represented by Structural Formula 2 below,
When X1 is a group represented by Structural Formula 2 below, either X2 or X3 is a group represented by Structural Formula 1 below,
[Structural Formula 1]

[Structural Formula 2]

In the structural formulas 1 and 2,
R11 and R12 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; A substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group,
L21 is a direct bond; Or a substituted or unsubstituted arylene group,
Y1 to Y3 are the same as or different from each other, each independently N or CRa, at least one of Y1 to Y3 is N,
Ra, R21 and R22 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; A substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group,
* means a position binding to Formula 1 above. The method according to claim 1, R11 and R12 are the same as or different from each other, each independently a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms; Or a compound that is a substituted or unsubstituted aryl group having 6 to 12 carbon atoms. The method according to claim 1, L21 is a direct bond; Or a compound that is a substituted or unsubstituted arylene group having 6 to 12 carbon atoms. The compound according to claim 1, wherein Y1 to Y3 are N. The method according to claim 1, wherein R21 and R22 are the same as or different from each other, and each independently a phenyl group unsubstituted or substituted with an alkyl group; Or a compound that is a substituted or unsubstituted biphenyl group. The compound according to claim 1, wherein the compound represented by Formula 1 is any one selected from the group consisting of the following compounds:

. An ink composition comprising the compound according to any one of claims 1 to 6. a first electrode;
a second electrode; and
Including one or more organic material layers provided between the first electrode and the second electrode,
At least one layer of the one or more layers of the organic material layer is an organic light emitting device comprising the ink composition of claim 7. The method according to claim 8, wherein the one or more organic material layers include a light emitting layer and one or more first organic material layers,
At least one layer of the one or more first organic material layers includes the ink composition. The organic light emitting device of claim 9, wherein the one or more first organic material layers are provided between the light emitting layer and the second electrode. The method according to claim 9, wherein the one or more first organic material layer is an electron injection layer; electron transport layer; and at least one of an electron injection and transport layer. An electronic device comprising the organic light emitting device according to claim 8. preparing a first electrode;
forming one or more organic material layers on the first electrode; and
Forming a second electrode on the one or more organic material layers;
The step of forming one or more organic material layers comprises forming an organic material layer using the ink composition according to claim 7 . The method of claim 13,
Forming an organic material layer using the ink composition
coating the ink composition on the first electrode or the one or more organic layers; and
Method of manufacturing an organic light emitting device comprising the step of drying or heat-treating the coated ink composition.

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