KR20220020447A - Compound and organic light emitting device comprising same - Google Patents

Abstract

The present specification provides a compound represented by chemical formula 1 and an organic light emitting device comprising the same. An exemplary embodiment of the present specification provides a compound represented by chemical formula 1. The compound according to at least one embodiment of the present specification can improve efficiency, lower driving voltage, and/or improve lifespan characteristics in the organic light emitting device.

Description

Compound and organic light emitting device comprising the same

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

In general, the organic light emitting phenomenon refers to a phenomenon in which electric energy is converted into light energy using an organic material. An organic light emitting device using an organic light emitting phenomenon generally has a structure including an anode and a cathode and an organic material layer therebetween. Here, the organic material layer is often formed of a multi-layered structure composed of different materials in order to increase the efficiency and stability of the organic 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, and the like. When a voltage is applied between the two electrodes in the structure of the organic light emitting device, holes are injected into the organic material layer from the anode and electrons from the cathode are injected into the organic material layer. When the injected holes and electrons meet, excitons are formed, and these excitons are When it falls back to the ground state, it lights up.

The development of new materials for the organic light emitting device as described above is continuously required.

KR 10-2014-0009918 A

The present specification provides a compound and an organic light emitting device including the same.

An exemplary embodiment of the present specification provides a compound represented by the following formula (1).

[Formula 1]

In Formula 1,

X1 to X3 are the same as or different from each other, each independently N or CR,

At least two of X1 to X3 are N,

L1 and L2 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted arylene group; Or a substituted or unsubstituted divalent heterocyclic group,

Ar1, Ar2 and R are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; nitrile group; nitro group; hydroxyl group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted aryloxy group; A substituted or unsubstituted alkylthio group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group, or a substituted or unsubstituted ring by combining with an adjacent group,

Ar3 and Ar4 are the same as or different from each other, and are each independently a substituted or unsubstituted alkyl group, or Ar3 and Ar4 are bonded to each other to form a substituted or unsubstituted aliphatic hydrocarbon ring,

R1 to R9 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; nitrile group; nitro group; hydroxyl group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted aryloxy group; A substituted or unsubstituted alkylthio group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group,

a is an integer of 0 to 6, and when a is 2 or more, 2 or more R9 are the same as or different from each other,

m and n are each an integer of 0 to 3, and when m and n are each 2 or more, L1 and L2 of two or more are the same as or different from each other,

L2 is connected to R1 to R8, Ar3 or Ar4.

In addition, one embodiment of the present specification is an anode; cathode; and at least one organic material layer provided between the anode and the cathode, wherein at least one of the organic material layers includes the compound represented by Formula 1 above.

The compound described herein may be used as a material for an organic layer of an organic light emitting device. The compound according to at least one exemplary embodiment of the present specification may improve efficiency, low driving voltage, and/or lifespan characteristics in an organic light emitting device. In particular, the compounds described herein can be used as hole injection, hole transport, hole injection and hole transport, electron blocking, light emission, hole blocking, electron transport, or electron injection material. In addition, compared to the conventional organic light emitting device, there is an effect of a low driving voltage, high efficiency, and/or a long lifespan.

1 shows an example of an organic light emitting device in which a substrate 1, an anode 2, a light emitting layer 6, and a cathode 8 are sequentially stacked.
2 shows a substrate 1, an anode 2, a hole injection layer 3, a first hole transport layer 4, a second hole transport layer 5, a light emitting layer 6, an electron transport and injection layer 7 and An example of an organic light emitting device in which the cathode 8 is sequentially stacked is shown.

Hereinafter, the present specification will be described in more detail.

In the present specification, when a part "includes" a certain component, this means that other components may be further included rather than excluding other components unless otherwise stated.

In this specification, when a member is said to be located "on" another member, this includes not only a case in which a member is in contact with another member but also a case in which another member exists between the two members.

"는 화학식 또는 화합물에 결합되는 위치를 의미한다.In this specification, "

" refers to the position bonded to the formula or compound.

Examples of substituents in the present specification are described below, but are not limited thereto.

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 position at which the hydrogen atom is substituted, that is, a position where the substituent is substitutable, is not limited, and when two or more are substituted , two or more substituents may be the same as or different from each other.

As used herein, the term "substituted or unsubstituted" refers to deuterium; halogen group; nitrile group (-CN); nitro group; hydroxyl group; an alkyl group; cycloalkyl group; alkoxy group; a phosphine oxide group; aryloxy group; alkyl thiooxy group; arylthioxy group; an alkyl sulfoxy group; arylsulfoxy group; alkenyl group; silyl group; boron group; amine group; aryl group; Or it means that it is substituted with one or more substituents selected from the group consisting of a heterocyclic group, is substituted with a substituent to which two or more of the above-exemplified substituents are connected, or does not have any substituents. 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 or may be interpreted as a substituent in which two phenyl groups are connected.

As used herein, the term "substituted or unsubstituted" refers to deuterium; halogen group; nitrile group; nitro group; hydroxyl group; amino group; silyl group; boron group; alkoxy group; aryloxy group; an alkyl group; cycloalkyl group; aryl group; And it means that it is substituted with one or two or more substituents selected from the group consisting of a heterocyclic group, is substituted with a substituent to which two or more of the above-exemplified substituents are connected, or does not have any substituents.

As used herein, the term "substituted or unsubstituted" refers to deuterium; halogen group; nitrile group; an alkyl group; aryl group; And it means that it is substituted with one or two or more substituents selected from the group consisting of a heterocyclic group, is substituted with a substituent to which two or more of the above-exemplified substituents are connected, or does not have any substituents.

Examples of the substituents are described below, but are not limited thereto.

In the present specification, examples of the halogen group include fluorine (-F), chlorine (-Cl), bromine (-Br), or iodine (-I).

In the present specification, the silyl group may be represented by the formula of -SiY _a Y _b Y _c , wherein Y _a , Y _b and Y _c are each hydrogen; a substituted or unsubstituted alkyl group; Or it may be a substituted or unsubstituted aryl group. The silyl group specifically includes, but is not limited to, 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. does not

In the present specification, the boron group may be represented by the formula of -BY _d Y _e , wherein Y _d and Y _e are each hydrogen; a substituted or unsubstituted alkyl group; Or it may be a substituted or unsubstituted aryl group. Specifically, the boron group includes, but is not limited to, a trimethylboron group, a triethylboron group, a t-butyldimethylboron group, a triphenylboron group, and a phenylboron group.

In the present specification, the alkyl group may be linear or branched, and the number of carbon atoms is not particularly limited, but is preferably 1 to 60. According to an exemplary embodiment, the number of carbon atoms in the alkyl group is 1 to 30. According to another exemplary embodiment, the alkyl group has 1 to 20 carbon atoms. According to another exemplary embodiment, the number of carbon atoms in the alkyl group is 1 to 10. Specific examples of the alkyl group include a methyl group, ethyl group, propyl group, n-propyl group, isopropyl group, butyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, n-pentyl group, hexyl group, n -hexyl group, heptyl group, n-heptyl group, octyl group, n-octyl group, etc., but are not limited thereto.

In the present specification, the description of the above-described alkyl group may be applied, except that the arylalkyl group is substituted with an aryl group.

In the present specification, the alkoxy group may be a straight chain, branched chain or cyclic chain. Although carbon number of an alkoxy group is not specifically limited, It is preferable that it is C1-C20. Specifically, methoxy, ethoxy, n-propoxy, isopropoxy, i-propyloxy, n-butoxy, isobutoxy, tert-butoxy, sec-butoxy, n-pentyloxy, neopentyloxy, isopentyloxy, n-hexyloxy, 3,3-dimethylbutyloxy, 2-ethylbutyloxy, n-octyloxy, n-nonyloxy, n-decyloxy, and the like, but is not limited thereto. .

The substituents containing an alkyl group, an alkoxy group, and other alkyl group moieties described herein include both straight-chain or pulverized forms.

In the present 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 an exemplary embodiment, the carbon number of the alkenyl group is 2 to 20. According to another exemplary embodiment, the carbon number of the alkenyl group is 2 to 10. According to another exemplary embodiment, the alkenyl group has 2 to 6 carbon atoms. Specific examples include 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, stilbenyl group, styrenyl group, and the like, but are not limited thereto.

In the present specification, the alkynyl group is a substituent including a triple bond between a carbon atom and a carbon atom, and may be linear or branched, and the number of carbon atoms is not particularly limited, but is preferably 2 to 40. According to an exemplary embodiment, the carbon number of the alkenyl group is 2 to 20. According to another exemplary embodiment, the carbon number of the alkenyl group is 2 to 10.

In the present specification, the cycloalkyl group is not particularly limited, but preferably has 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 carbon number of the cycloalkyl group is 3 to 20. According to another exemplary embodiment, the cycloalkyl group has 3 to 6 carbon atoms. Specifically, there are a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, and the like, but is not limited thereto.

In the present specification, the amine group is -NH ₂ , and the amine group may be substituted with the above-described alkyl group, aryl group, heterocyclic group, alkenyl group, cycloalkyl group, and combinations thereof. The number of carbon atoms of the substituted amine group is not particularly limited, but is preferably 1 to 30. According to an exemplary embodiment, the carbon number of the amine group is 1 to 20. According to an exemplary embodiment, the carbon number of the amine group is 1 to 10. Specific examples of the substituted amine group include a methylamine group, a dimethylamine group, an ethylamine group, a diethylamine group, a phenylamine group, a 9,9-dimethylfluorenylphenylamine group, a pyridylphenylamine group, and a diphenylamine group. group, phenylpyridylamine group, naphthylamine group, biphenylamine group, anthracenylamine group, dibenzofuranylphenylamine group, 9-methylanthracenylamine group, diphenylamine group, phenylnaphthylamine group, There is a ditolylamine group, a phenyltolylamine group, a diphenylamine group, and the like, but is not limited thereto.

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 an exemplary embodiment, the carbon number of the aryl group is 6 to 30. According to an exemplary embodiment, the carbon number of the aryl group is 6 to 20. The aryl group may be a monocyclic aryl group, such as a phenyl group, a biphenyl group, a terphenyl group, or a quaterphenyl group, but is not limited thereto. The polycyclic aryl group may be a naphthyl group, anthracenyl group, phenanthrenyl group, pyrenyl group, perylenyl group, triphenyl group, chrysenyl group, fluorenyl group, triphenylenyl group, etc., but is not limited thereto not.

In the present specification, the fluorenyl group may be substituted, and two substituents may be bonded to each other to form a spiro structure. In this case, the spiro structure may be an aromatic hydrocarbon ring or an aliphatic hydrocarbon ring.

,

,

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-dimethyl fluorenyl group), and

a substituted fluorenyl group such as (9,9-diphenylfluorenyl group). However, the present invention is not limited thereto.

In the present specification, the description of the above-described aryl group may be applied to the aryl group in the aryloxy group.

In the present specification, the description of the above-described alkyl group may be applied to the alkyl group in the alkylthiooxy group and the alkylsulfoxy group.

In the present specification, the description of the above-described aryl group may be applied to the aryl group in the arylthioxy group and the arylsulfoxy group.

In the present specification, the heterocyclic group is a cyclic group including at least one of N, O, P, S, Si and Se as heteroatoms, and the number of carbon atoms is not particularly limited, but preferably has 2 to 60 carbon atoms. According to an exemplary embodiment, the heterocyclic group has 2 to 30 carbon atoms. According to an exemplary embodiment, the heterocyclic group has 2 to 20 carbon atoms. Examples of the heterocyclic group include a pyridine group, a pyrrole group, a pyrimidine group, a quinoline group, a pyridazinyl group, a furan group, a thiophene group, an imidazole group, a pyrazole group, a dibenzofuran group, a dibenzothiophene group , a carbazole group, a benzocarbazole group, a naphthobenzofuran group, a benzonaphthothiophene group, an indenocarbazole group, a triazinyl group, and the like, but are not limited thereto.

In the present specification, the description of the above-described heterocyclic group may be applied, except that the heteroaryl group is aromatic.

In the present specification, the description of the alkenyl group may be applied except that the alkenylene group is divalent.

In the present specification, the description of the aryl group may be applied except that the arylene group is divalent.

In the present specification, the description of the heterocyclic group may be applied, except that the divalent heterocycle is divalent.

In the present specification, in a substituted or unsubstituted ring formed by bonding with an adjacent group, "ring" is a hydrocarbon ring; or a heterocyclic ring.

The hydrocarbon ring may be an aromatic, aliphatic, or a condensed ring of an aromatic and an aliphatic group, and may be selected from examples of the cycloalkyl group or the aryl group.

In the present specification, the meaning of forming a ring by bonding with adjacent groups means a substituted or unsubstituted aliphatic hydrocarbon ring by bonding with adjacent groups; a substituted or unsubstituted aromatic hydrocarbon ring; substituted or unsubstituted aliphatic heterocycle; substituted or unsubstituted aromatic heterocycle; Or it means to form a condensed ring thereof. The hydrocarbon ring means a ring consisting of only carbon and hydrogen atoms. The heterocycle means a ring including at least one selected from elements such as N, O, P, S, Si and Se. In the present specification, the aliphatic hydrocarbon ring, the aromatic hydrocarbon ring, the aliphatic heterocycle and the aromatic heterocycle may be monocyclic or polycyclic.

In the present specification, the aliphatic hydrocarbon ring is a non-aromatic ring and refers to a ring consisting only of carbon and hydrogen atoms. Examples of the aliphatic hydrocarbon ring include cyclopropane, cyclobutane, cyclobutene, cyclopentane, cyclopentene, cyclohexane, cyclohexene, 1,4-cyclohexadiene, cycloheptane, cycloheptene, cyclooctane, cyclooctene, etc. However, the present invention is not limited thereto.

In the present specification, the aromatic hydrocarbon ring means an aromatic ring consisting only of carbon and hydrogen atoms. Examples of the aromatic hydrocarbon ring include benzene, naphthalene, anthracene, phenanthrene, perylene, fluoranthene, triphenylene, phenalene, pyrene, tetracene, chrysene, pentacene, fluorene, indene, acenaphthylene, benzofluorene, spirofluorene, and the like, but is not limited thereto. In the present specification, the aromatic hydrocarbon ring may be interpreted as having the same meaning as the aryl group.

In the present specification, the aliphatic heterocycle refers to an aliphatic ring including one or more heteroatoms. Examples of aliphatic heterocycles include oxirane, tetrahydrofuran, 1,4-dioxane, pyrrolidine, piperidine, morpholine, oxepane, azocaine , thiocaine, and the like, but are not limited thereto.

In the present specification, the aromatic heterocycle refers to an aromatic ring including one or more heteroatoms. Examples of aromatic heterocycles include pyridine, pyrrole, pyrimidine, pyridazine, furan, thiophene, imidazole, paraazole, oxazole, isoxazole, thiazole, isothiazole, triazole, oxadiazole, thiazole. Diazole, dithiazole, tetrazole, pyran, thiopyran, diazine, oxazine, thiazine, dioxin, triazine, tetrazine, isoquinoline, quinoline, quinone, quinazoline, quinoxaline, naphthyridine, acridine , phenanthridine, diazanaphthalene, driazaindene, indole, indolizine, benzothiazole, benzoxazole, benzoimidazole, benzothiophene, benzofuran, dibenzothiophene, dibenzofuran, carbazole, benzo carbazole, dibenzocarbazole, phenazine, imidazopyridine, phenoxazine, indolocarbazole, indenocarbazole, and the like, but is not limited thereto.

Hereinafter, preferred embodiments of the present invention will be described in detail. However, the embodiment of the present invention may be modified in various forms, and the scope of the present invention is not limited to the embodiments described below.

When the compound represented by Formula 1 is applied to an organic light emitting device, an organic light emitting device having high efficiency, low voltage and/or long lifespan may be obtained.

Hereinafter, Chemical Formula 1 will be described in detail.

[Formula 1]

In Formula 1,

X1 to X3 are the same as or different from each other, each independently N or CR,

At least two of X1 to X3 are N,

L1 and L2 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted arylene group; Or a substituted or unsubstituted divalent heterocyclic group,

Ar1, Ar2 and R are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; nitrile group; nitro group; hydroxyl group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted aryloxy group; A substituted or unsubstituted alkylthio group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group, or a substituted or unsubstituted ring by combining with an adjacent group,

Ar3 and Ar4 are the same as or different from each other, and are each independently a substituted or unsubstituted alkyl group, or Ar3 and Ar4 are bonded to each other to form a substituted or unsubstituted aliphatic hydrocarbon ring,

R1 to R9 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; nitrile group; nitro group; hydroxyl group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted aryloxy group; A substituted or unsubstituted alkylthio group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group,

a is an integer of 0 to 6, and when a is 2 or more, 2 or more R9 are the same as or different from each other,

m and n are each an integer of 0 to 3, and when m and n are each 2 or more, L1 and L2 of two or more are the same as or different from each other,

L2 is connected to R1 to R8, Ar3 or Ar4.

In the exemplary embodiment of the present specification, X1 and X2 are N, and X3 is CR.

In an exemplary embodiment of the present specification, X2 and X3 are N, and X1 is CR.

In the exemplary embodiment of the present specification, X1 and X3 are N, and X2 is CR.

In an exemplary embodiment of the present specification, X1 to X3 are N.

In an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted arylene group; Or a substituted or unsubstituted divalent heterocyclic group.

In an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted monocyclic to tetracyclic arylene group; or a substituted or unsubstituted monocyclic to 4-ring divalent heterocyclic group.

In an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted monocyclic to bicyclic arylene group; or a substituted or unsubstituted monocyclic to bicyclic divalent heterocyclic group.

In an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted arylene group having 6 to 60 carbon atoms; or a substituted or unsubstituted divalent heterocyclic group having 2 to 60 carbon atoms.

In an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted arylene group having 6 to 30 carbon atoms; Or a substituted or unsubstituted divalent heterocyclic group having 2 to 30 carbon atoms.

In an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted arylene group having 6 to 20 carbon atoms; or a substituted or unsubstituted C 2 to C 20 divalent heterocyclic group.

In an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently a direct bond; an arylene group unsubstituted or substituted with an alkyl group; or a divalent heterocyclic group unsubstituted or substituted with an alkyl group.

In an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently a direct bond; an arylene group unsubstituted or substituted with an alkyl group; or a substituted or unsubstituted N-containing monocyclic or bicyclic divalent heterocyclic ring.

In an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted phenylene group; a substituted or unsubstituted biphenylene group; a substituted or unsubstituted naphthylene group; a substituted or unsubstituted divalent pyridine group; A substituted or unsubstituted divalent pyridazine group; or a substituted or unsubstituted divalent quinazoline group.

In an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently a direct bond; a phenylene group unsubstituted or substituted with a methyl group; biphenylene group; naphthylene group; a divalent pyridine group; divalent pyridazine group; or a divalent quinazoline group.

In an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently a direct bond; a phenylene group unsubstituted or substituted with a methyl group; biphenylene group; naphthylene group; a divalent pyridine group; or a divalent pyridazine group.

In an exemplary embodiment of the present specification, Ar1, Ar2, and R are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; nitrile group; nitro group; hydroxyl group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted aryloxy group; A substituted or unsubstituted alkylthio group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group, or a substituted or unsubstituted ring by combining with an adjacent group.

In an exemplary embodiment of the present specification, Ar1, Ar2, and R are the same as or different from each other, and each independently hydrogen; heavy hydrogen; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group.

In an exemplary embodiment of the present specification, Ar1, Ar2, and R are the same as or different from each other, and each independently hydrogen; heavy hydrogen; a substituted or unsubstituted C 1 to C 60 alkyl group; a substituted or unsubstituted C 3 to C 60 cycloalkyl group; a substituted or unsubstituted aryl group having 6 to 60 carbon atoms; Or a substituted or unsubstituted heterocyclic group having 2 to 60 carbon atoms.

In an exemplary embodiment of the present specification, Ar1, Ar2, and R are the same as or different from each other, and each independently hydrogen; heavy hydrogen; a substituted or unsubstituted C 1 to C 30 alkyl group; a substituted or unsubstituted C 3 to C 30 cycloalkyl group; a substituted or unsubstituted C6-C30 aryl group; Or a substituted or unsubstituted heterocyclic group having 2 to 30 carbon atoms.

In an exemplary embodiment of the present specification, Ar1, Ar2, and R are the same as or different from each other, and each independently hydrogen; heavy hydrogen; a substituted or unsubstituted C 1 to C 20 alkyl group; a substituted or unsubstituted C 3 to C 20 cycloalkyl group; a substituted or unsubstituted C6-C20 aryl group; Or a substituted or unsubstituted heterocyclic group having 2 to 20 carbon atoms.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; a substituted or unsubstituted alkyl group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently a substituted or unsubstituted alkyl group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently a substituted or unsubstituted C 1 to C 60 alkyl group; a substituted or unsubstituted aryl group having 6 to 60 carbon atoms; Or a substituted or unsubstituted heterocyclic group having 2 to 60 carbon atoms.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently a substituted or unsubstituted C 1 to C 30 alkyl group; a substituted or unsubstituted C6-C30 aryl group; Or a substituted or unsubstituted heterocyclic group having 2 to 30 carbon atoms.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently a substituted or unsubstituted C 1 to C 20 alkyl group; a substituted or unsubstituted C6-C20 aryl group; Or a substituted or unsubstituted heterocyclic group having 2 to 20 carbon atoms.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently an alkyl group unsubstituted or substituted with a cyano group, an alkyl group, or a heterocyclic group; an aryl group unsubstituted or substituted with a cyano group, an alkyl group, or a heterocyclic group; or a heterocyclic group unsubstituted or substituted with a cyano group, an alkyl group, or a heterocyclic group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently a substituted or unsubstituted methyl group; a substituted or unsubstituted butyl group; a substituted or unsubstituted phenyl group; a substituted or unsubstituted biphenyl group; a substituted or unsubstituted naphthyl group; a substituted or unsubstituted phenanthrenyl group; a substituted or unsubstituted phenalene group; a substituted or unsubstituted fluoranthene group; a substituted or unsubstituted fluorenyl group; a substituted or unsubstituted pyridyl group; a substituted or unsubstituted carbazole group; Or a substituted or unsubstituted dibenzofuran group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently a substituted or unsubstituted methyl group; a substituted or unsubstituted butyl group; a substituted or unsubstituted phenyl group; a substituted or unsubstituted biphenyl group; a substituted or unsubstituted naphthyl group; a substituted or unsubstituted phenanthrenyl group; a substituted or unsubstituted phenalene group; a substituted or unsubstituted fluoranthene group; a substituted or unsubstituted fluorenyl group; a substituted or unsubstituted spirofluorenyl group; a substituted or unsubstituted pyridyl group; a substituted or unsubstituted carbazole group; Or a substituted or unsubstituted dibenzofuran group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently a methyl group unsubstituted or substituted with a cyano group, a methyl group, or a pyridyl group; a butyl group unsubstituted or substituted with a cyano group, a methyl group, or a pyridyl group; a phenyl group unsubstituted or substituted with a cyano group, a methyl group, or a pyridyl group; a biphenyl group unsubstituted or substituted with a cyano group, a methyl group, or a pyridyl group; a naphthyl group unsubstituted or substituted with a cyano group, a methyl group, or a pyridyl group; a phenanthrenyl group unsubstituted or substituted with a cyano group, a methyl group, or a pyridyl group; a phenalene group unsubstituted or substituted with a cyano group, a methyl group, or a pyridyl group; a fluoranthene group unsubstituted or substituted with a cyano group, a methyl group, or a pyridyl group; a fluorenyl group unsubstituted or substituted with a cyano group, a methyl group, a cyclohexyl group, or a pyridyl group; a spirofluorenyl group unsubstituted or substituted with a cyano group, a methyl group, a cyclohexyl group, or a pyridyl group; a pyridyl group unsubstituted or substituted with a cyano group, a methyl group, or a pyridyl group; a carbazole group unsubstituted or substituted with a cyano group, a methyl group, or a pyridyl group; or a dibenzofuran group unsubstituted or substituted with a cyano group, a methyl group, or a pyridyl group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently a methyl group; butyl group; a phenyl group unsubstituted or substituted with a methyl group or a pyridyl group; a biphenyl group unsubstituted or substituted with a cyano group; naphthyl group; phenanthrenyl group; phenalene group; fluoranthene group; spirocyclohexanefluorenyl group; a pyridyl group unsubstituted or substituted with a methyl group; a carbazole group; or a dibenzofuran group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently a methyl group; t-butyl group; a phenyl group unsubstituted or substituted with a methyl group or a pyridyl group; a biphenyl group unsubstituted or substituted with a cyano group; naphthyl group; phenanthrenyl group; phenalene group; fluoranthene group; a spiro[cyclohexane-1,9'-fluorene] group; a pyridyl group unsubstituted or substituted with a methyl group; a carbazole group; or a dibenzofuran group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently a methyl group; t-butyl group; a phenyl group unsubstituted or substituted with a methyl group or a pyridyl group; a biphenyl group unsubstituted or substituted with a cyano group; naphthyl group; fluoranthene group; a pyridyl group unsubstituted or substituted with a methyl group; N-carbazole group; or a dibenzofuran group.

In an exemplary embodiment of the present specification, R is hydrogen; heavy hydrogen; a substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group.

In an exemplary embodiment of the present specification, R is hydrogen; heavy hydrogen; a substituted or unsubstituted C 1 to C 60 alkyl group; or a substituted or unsubstituted C6-C60 aryl group.

In an exemplary embodiment of the present specification, R is hydrogen; heavy hydrogen; a substituted or unsubstituted C 1 to C 30 alkyl group; or a substituted or unsubstituted C6-C30 aryl group.

In an exemplary embodiment of the present specification, R is hydrogen; heavy hydrogen; a substituted or unsubstituted C 1 to C 20 alkyl group; or a substituted or unsubstituted C6-C20 aryl group.

In an exemplary embodiment of the present specification, R is hydrogen; heavy hydrogen; a substituted or unsubstituted methyl group; or a substituted or unsubstituted phenyl group.

In an exemplary embodiment of the present specification, R is hydrogen; heavy hydrogen; methyl group; or a phenyl group.

In an exemplary embodiment of the present specification, R is hydrogen; methyl group; or a phenyl group.

In an exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, and each independently represent a substituted or unsubstituted alkyl group, or Ar3 and Ar4 combine with each other to form a substituted or unsubstituted aliphatic hydrocarbon ring.

In an exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, and each independently a substituted or unsubstituted C 1 to C 60 alkyl group, or Ar3 and Ar4 are bonded to each other and substituted or unsubstituted C 3 to 60 aliphatic hydrocarbon rings.

In the exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, and each independently a substituted or unsubstituted C 1 to C 30 alkyl group, or Ar3 and Ar4 are bonded to each other and substituted or unsubstituted C 3 to 30 aliphatic hydrocarbon rings.

In an exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, and each independently is a substituted or unsubstituted C 1 to C 20 alkyl group, or Ar3 and Ar4 are bonded to each other and substituted or unsubstituted C 3 to 20 aliphatic hydrocarbon rings.

In the exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, and each independently a substituted or unsubstituted C1 to C10 alkyl group, or Ar3 and Ar4 are bonded to each other to have a substituted or unsubstituted C3 to 10 aliphatic hydrocarbon rings.

In an exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, and each independently is an alkyl group having 1 to 10 carbon atoms, or Ar3 and Ar4 are bonded to each other to form an aliphatic hydrocarbon ring having 3 to 10 carbon atoms.

In an exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, and each independently is an alkyl group having 1 to 4 carbon atoms, or Ar3 and Ar4 are bonded to each other to form an aliphatic hydrocarbon ring having 3 to 10 carbon atoms.

In the exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, each independently an alkyl group, or Ar3 and Ar4 are bonded to each other to form an aliphatic hydrocarbon ring.

In an exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, and each independently a substituted or unsubstituted methyl group; a substituted or unsubstituted ethyl group; a substituted or unsubstituted propyl group; Or a substituted or unsubstituted butyl group, Ar3 and Ar4 combine with each other to form a substituted or unsubstituted cyclohexane ring.

In an exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, and each independently a methyl group; ethyl group; Profile group; or a butyl group, or Ar3 and Ar4 combine with each other to form a cyclohexane ring.

In an exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, and each independently a methyl group; ethyl group; n-propyl group; or a t-butyl group, or Ar3 and Ar4 combine with each other to form a cyclohexane ring.

In an exemplary embodiment of the present specification, Ar3 and Ar4 are the same as or different from each other, and each independently a methyl group; n-propyl group; or a t-butyl group, or Ar3 and Ar4 combine with each other to form a cyclohexane ring.

In an exemplary embodiment of the present specification, R1 to R9 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; nitrile group; nitro group; hydroxyl group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted aryloxy group; A substituted or unsubstituted alkylthio group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group.

In an exemplary embodiment of the present specification, R1 to R9 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; nitrile group; a substituted or unsubstituted C 1 to C 60 alkyl group; a substituted or unsubstituted aryl group having 6 to 60 carbon atoms; Or a substituted or unsubstituted heterocyclic group having 2 to 60 carbon atoms.

In an exemplary embodiment of the present specification, R1 to R9 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; nitrile group; a substituted or unsubstituted C 1 to C 30 alkyl group; a substituted or unsubstituted C6-C30 aryl group; Or a substituted or unsubstituted heterocyclic group having 2 to 30 carbon atoms.

In an exemplary embodiment of the present specification, R1 to R9 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; nitrile group; a substituted or unsubstituted C 1 to C 20 alkyl group; a substituted or unsubstituted C6-C20 aryl group; Or a substituted or unsubstituted heterocyclic group having 2 to 20 carbon atoms.

In an exemplary embodiment of the present specification, R1 to R9 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; nitrile group; an alkyl group unsubstituted or substituted with a halogen group; an aryl group unsubstituted or substituted with a halogen group; Or a heterocyclic group substituted or unsubstituted with a halogen group.

In an exemplary embodiment of the present specification, R1 to R9 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; nitrile group; an alkyl group unsubstituted or substituted with a halogen group; aryl group; or a heterocyclic group.

In an exemplary embodiment of the present specification, R1 to R9 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; nitrile group; a substituted or unsubstituted methyl group; a substituted or unsubstituted phenyl group; Or a substituted or unsubstituted pyridyl group.

In an exemplary embodiment of the present specification, R1 to R9 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; nitrile group; a methyl group unsubstituted or substituted with a fluoro group (-F); phenyl group; or a pyridyl group.

In an exemplary embodiment of the present specification, R1 to R8 are the same as or different from each other, and each independently hydrogen; nitrile group; a methyl group unsubstituted or substituted with a fluoro group (-F); phenyl group; or a pyridyl group.

In an exemplary embodiment of the present specification, R1 to R8 are the same as or different from each other, and each independently hydrogen; nitrile group; methyl group; -CF ₃ ; phenyl group; or a pyridyl group.

In an exemplary embodiment of the present specification, R1 to R8 are hydrogen; or deuterium.

In an exemplary embodiment of the present specification, R1 to R8 are hydrogen.

In an exemplary embodiment of the present specification, R9 is hydrogen; or deuterium.

In an exemplary embodiment of the present specification, R9 is hydrogen.

In the exemplary embodiment of the present specification, a is 0.

In one embodiment of the present specification, a is 1.

In one embodiment of the present specification, a is 6.

In the exemplary embodiment of the present specification, m and n are each 0.

In one embodiment of the present specification, m and n are each 1.

In one embodiment of the present specification, m and n are each 2.

In the exemplary embodiment of the present specification, each of m and n is 3.

In the exemplary embodiment of the present specification, L2 is connected to R1.

In the exemplary embodiment of the present specification, L2 is connected to R2.

In the exemplary embodiment of the present specification, L2 is connected to R3.

In the exemplary embodiment of the present specification, L2 is connected to R4.

In the exemplary embodiment of the present specification, L2 is connected to Ar3.

In the exemplary embodiment of the present specification, L2 is connected to Ar4.

In the exemplary embodiment of the present specification, Chemical Formula 1 is represented by any one of the following Chemical Formulas 1-1 to 1-5.

[Formula 1-1]

[Formula 1-2]

[Formula 1-3]

[Formula 1-4]

[Formula 1-5]

In Formulas 1-1 to 1-5,

Definitions of X1 to X3, L1, L2, Ar1 to Ar4, R1 to R9, a, m, and n are the same as those in Formula 1 above.

In an exemplary embodiment of the present specification, Chemical Formula 1 is represented by any one of the following compounds.

The compound represented by Formula 1 according to an exemplary embodiment of the present specification may have a core structure as shown in Scheme 1 or Scheme 2 below. Substituents may be combined by methods known in the art, and the type, position or number of substituents may be changed according to techniques known in the art.

<Scheme 1>

<Scheme 2>

In Schemes 1 and 2, the definition of the substituent is the same as the definition in Formula 1 above, X is a halogen group (Br, Cl, I, etc.), -SO ₃ C ₄ F ₉ , -SO ₃ CF ₃ , etc., R _x is hydrogen; It is a substituted or unsubstituted alkyl group, or the like, or combines with an adjacent group to form dioxaborolane.

In Schemes 1 and 2, the process of synthesizing a compound having a specific substituent bonded to a specific position was exemplified, but the above formula Compounds corresponding to the range of 1 can be synthesized.

In the present specification, compounds having various energy band gaps can be synthesized by introducing various substituents into the core structure of the compound represented by Formula 1 above. In addition, in the present specification, the HOMO and LUMO energy levels of the compound can be controlled by introducing various substituents into the core structure of the structure as described above.

In addition, the present specification provides an organic light emitting device including the above-described compound.

In the present specification, when a member is said to be located “on” another member, this includes not only a case in which a member is in contact with another member but also a case in which another member is present between the two members.

In the present specification, when a part "includes" a certain component, it means that other components may be further included, rather than excluding other components, unless otherwise stated.

The organic light emitting device according to the present specification includes an anode; cathode; and at least one organic material layer provided between the anode and the cathode, wherein at least one of the organic material layers comprises a compound represented by Formula 1 above.

The organic light emitting device of the present specification may be manufactured by a conventional method and material for manufacturing an organic light emitting device, except for forming an organic material layer using the compound of Formula 1 above.

The compound may be formed into an organic material layer by a solution coating method as well as a vacuum deposition method when manufacturing an organic light emitting device. Here, the solution coating method refers to spin coating, dip coating, inkjet printing, screen printing, spraying, roll coating, and the like, but is not limited thereto.

The organic material layer of the organic light emitting device of the present specification may have a single-layer structure, but may have a multi-layer structure in which two or more organic material layers are stacked. For example, the organic light emitting device of the present invention comprises at least one of a hole transport layer, a hole injection layer, an electron blocking layer, a hole transport and injection layer, an electron transport layer, an electron injection layer, a hole blocking layer, and an electron transport and injection layer as an organic material layer. It may have a structure that includes However, the structure of the organic light emitting device of the present specification is not limited thereto and may include a smaller number or a larger number of organic material layers.

In the organic light emitting device of the present specification, the organic material layer includes a hole injection layer, a hole transport layer, or a hole injection and transport layer, and the hole injection layer, the hole transport layer, or the hole injection and transport layer is a compound represented by the above formula (1) may include

In the organic light emitting device of the present specification, the organic material layer may include a hole transport layer or a hole injection layer, and the hole transport layer or the hole injection layer may include the compound represented by Chemical Formula 1 described above.

In one embodiment of the present specification, the organic material layer includes an electron injection layer, an electron transport layer, an electron transport and injection layer or a hole blocking layer, and the electron injection layer, the electron transport layer, the electron transport and injection layer or the hole blocking layer is It may include a compound represented by Formula 1 described above.

In the organic light emitting device of the present specification, the organic material layer includes an electron transport layer, an electron injection layer, or an electron transport and injection layer, and the electron transport layer, the electron injection layer, or the electron transport and injection layer is represented by the above formula (1) compounds may be included.

In an exemplary embodiment of the present specification, the organic material layer may include an electron control layer, and the electron control layer may include the compound represented by Formula 1 described above.

In an exemplary embodiment of the present specification, the organic material layer includes a hole blocking layer, and the hole blocking layer includes a compound represented by Formula 1 above.

In the organic light emitting device of the present specification, the organic material layer is an electron transport and injection layer, and the electron transport and injection layer includes the compound represented by Chemical Formula 1 described above.

In an exemplary embodiment of the present specification, the thickness of the organic material layer including the compound of Formula 1 is 5 nm to 200 nm, preferably 10 nm to 200 nm, and more preferably 10 nm to 50 nm.

In an exemplary embodiment of the present specification, the organic material layer includes a light emitting layer, and the light emitting layer includes the compound represented by Formula 1 described above.

In an exemplary embodiment of the present specification, the organic material layer includes a light emitting layer, and the light emitting layer includes the compound represented by Formula 1 as a host.

In the exemplary embodiment of the present specification, the organic material layer includes an emission layer, and the emission layer includes the compound represented by Formula 1 as a dopant.

In another exemplary embodiment, the organic material layer may further include other organic compounds, metals, or metal compounds in addition to the compound represented by Formula 1 above.

In the organic light emitting device according to the exemplary embodiment of the present specification, the light emitting layer further includes a fluorescent dopant or a phosphorescent dopant. In this case, the dopant in the light emitting layer is included in an amount of 1 to 50 parts by weight based on 100 parts by weight of the host.

As another example, the organic material layer may include an emission layer, the emission layer may include the compound represented by Formula 1 as a host, and may further include an additional host.

In an exemplary embodiment of the present specification, the dopant includes an arylamine-based compound, a heterocyclic compound including boron and nitrogen, or an Ir complex.

The organic light emitting device of the present specification may further include an organic material layer of at least one of a hole transport layer, a hole injection layer, an electron blocking layer, an electron transport and injection layer, an electron transport layer, an electron injection layer, a hole blocking layer, and a hole transport and injection layer. can

In an exemplary embodiment of the present specification, the organic light emitting device includes an anode; cathode; and two or more organic material layers provided between the anode and the cathode, wherein at least one of the two or more organic material layers includes the compound represented by Formula 1 above.

In an exemplary embodiment of the present specification, two or more organic material layers may be selected from the group consisting of a light emitting layer, a hole transport layer, a hole injection layer, a hole transport and injection layer, and an electron blocking layer.

In an exemplary embodiment of the present specification, two or more organic material layers may be selected from the group consisting of a light emitting layer, an electron transport layer, an electron injection layer, an electron transport and injection layer, an electron control layer, and a hole blocking layer.

In the exemplary embodiment of the present specification, the organic material layer includes two or more electron transport layers, and at least one of the two or more electron transport layers includes the compound represented by Formula 1 above. Specifically, in an exemplary embodiment of the present specification, the compound represented by Formula 1 may be included in one of the two or more electron transport layers, or may be included in each of the two or more electron transport layers.

In addition, in the exemplary embodiment of the present specification, when the compound is included in each of the two or more electron transport layers, materials other than the compound represented by Formula 1 may be the same or different from each other.

When the organic material layer including the compound represented by Formula 1 is an electron transport layer, an electron injection layer, or an electron transport and injection layer, the electron transport layer, the electron injection layer, or the electron transport and injection layer may further include an n-type dopant. can As the n-type dopant, those known in the art may be used, for example, a metal or a metal complex may be used. For example, the electron transport layer including the compound represented by Formula 1 may further include lithium quinolate (LiQ). According to an example, the compound represented by Formula 1 and the n-type dopant may be included in a weight ratio of 2:8 to 8:2, for example, 4:6 to 6:4.

According to an example, the compound represented by Formula 1 and the n-type dopant may be included in a weight ratio of 1:1.

In an exemplary embodiment of the present specification, the organic material layer includes two or more hole transport layers, and at least one of the two or more hole transport layers includes the compound represented by Formula 1 above. Specifically, in an exemplary embodiment of the present specification, the compound represented by Formula 1 may be included in one of the two or more hole transport layers, and may be included in each of the two or more hole transport layers.

In addition, in an exemplary embodiment of the present specification, when the compound represented by Formula 1 is included in each of the two or more hole transport layers, materials other than the compound represented by Formula 1 may be the same or different from each other. there is.

In an exemplary embodiment of the present specification, the organic material layer includes a hole injection layer or a hole transport layer containing a compound including an arylamine group, a carbazolyl group or a benzocarbazolyl group in addition to the organic material layer including the compound represented by Formula 1 may include

In the exemplary embodiment of the present specification, 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.

In the exemplary embodiment of the present specification, 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.

In the organic light emitting device of the present invention, the organic material layer may include an electron blocking layer, the electron blocking layer may be a material known in the art.

The organic light emitting device may have, for example, a stacked structure as follows, 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 / light emitting layer / electron transport layer / cathode

(11) anode / hole transport layer / electron blocking layer / light emitting 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

The structure of the organic light emitting diode of the present specification may have a structure as shown in FIGS. 1 and 2 , but is not limited thereto.

1 illustrates a structure of an organic light emitting device in which a substrate 1, an anode 2, a light emitting layer 6, and a cathode 8 are sequentially stacked. In such a structure, the compound may be included in the light emitting layer 6 .

2 shows a substrate 1, an anode 2, a hole injection layer 3, a first hole transport layer 4, a second hole transport layer 5, a light emitting layer 6, an electron transport and injection layer 7 and The structure of the organic light emitting device in which the cathode 8 is sequentially stacked is illustrated. In such a structure, the compound may be included in the hole injection layer 3 , the first hole transport layer 4 , the second hole transport layer 5 , the light emitting layer 6 or the electron transport and injection layer 7 . .

In one embodiment of the present specification, the electron transport and injection layer and the light emitting layer may be provided adjacent to each other.

In one embodiment of the present specification, the electron control layer and the light emitting layer may be provided adjacent to each other.

In an exemplary embodiment of the present specification, the hole blocking layer and the light emitting layer may be provided adjacent to each other.

In one embodiment of the present specification, the hole blocking layer and the electron transport layer may be provided adjacent to each other.

The organic light emitting device of the present specification may be manufactured using materials and methods known in the art, except that at least one layer of the organic material layer includes the compound, that is, the compound represented by Formula 1 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.

For example, the organic light emitting device according to the present specification uses a PVD (physical vapor deposition) method such as sputtering or e-beam evaporation to form a metal or a conductive metal oxide or an alloy thereof on a substrate. is deposited to form an anode, and an organic material layer including a hole injection layer, a hole transport layer, a light emitting layer, an electron blocking layer, an electron transport layer and an electron injection layer is formed thereon, and then a material that can be used as a cathode is deposited thereon. can be 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.

The organic material layer may further include at least one of a hole transport layer, a hole injection layer, an electron blocking layer, an electron transport and injection layer, an electron transport layer, an electron injection layer, a hole blocking layer, and a hole transport and injection layer.

The organic material layer may have a multilayer structure including a hole injection layer, a hole transport layer, an electron transport and injection layer, an electron blocking layer, a light emitting layer and an electron transport layer, an electron injection layer, an electron transport and injection layer, etc., but is not limited thereto, but a single layer structure can be In addition, the organic layer is formed using a variety of polymer materials in a smaller number by a solvent process rather than a vapor deposition method, such as spin coating, dip coating, doctor blading, screen printing, inkjet printing, or thermal transfer method. It can be made in layers.

The anode is an electrode for injecting holes, and the anode material is usually preferably a material having a large work function so that holes can be smoothly injected into the organic material layer. Specific examples of the anode material that can be used in the present invention include metals such as vanadium, chromium, copper, zinc, gold, or alloys thereof; metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO, Indium Tin Oxide), and indium zinc oxide (IZO, Indium Zinc Oxide); ZnO: Al or SnO ₂ : Combination of metals and oxides 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 is an electrode for injecting electrons, and the cathode material is preferably a material having a small work function to facilitate electron injection into the organic material layer. Specific examples of the cathode material include metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin and lead, or alloys thereof; and a multi-layered material such as LiF/Al or LiO ₂ /Al, but is not limited thereto.

The hole injection layer is a layer that smoothly injects holes from the anode into the light emitting layer. As the hole injection material, holes can be well injected from the anode at a low voltage, and the highest occupied (HOMO) of the hole injection material is The molecular orbital) is preferably between the work function of the anode material and the HOMO of the surrounding organic layer. Specific examples of the hole injection material include metal porphyrine, oligothiophene, arylamine-based organic material, hexanitrile hexaazatriphenylene-based organic material, quinacridone-based organic material, and perylene-based organic material. of organic substances, anthraquinones, polyaniline and polythiophene-based conductive polymers, and the like, but are not limited thereto. The hole injection layer may have a thickness of 1 to 150 nm. When the thickness of the hole injection layer is 1 nm or more, there is an advantage in that the hole injection characteristics can be prevented from being deteriorated, and when it is 150 nm or less, the thickness of the hole injection layer is too thick, so that the driving voltage is increased to improve hole movement There are advantages to avoiding this.

The hole transport layer may serve to facilitate hole transport. As the hole transport material, a material capable of receiving holes from the anode or hole injection layer and transferring them to the light emitting layer is suitable, and a material having high hole mobility is suitable. Specific examples include, but are not limited to, an arylamine-based organic material, a conductive polymer, and a block copolymer having a conjugated portion and a non-conjugated portion together.

An additional hole buffer layer may be provided between the hole injection layer and the hole transport layer, and may include hole injection or transport materials known in the art.

An electron blocking layer may be provided between the hole transport layer and the light emitting layer. The above-described compound or a material known in the art may be used for the electron blocking layer.

The light emitting layer may emit red, green, or blue light, and may be made of a phosphorescent material or a fluorescent material. The light emitting material is a material capable of emitting light in the visible ray region by receiving and combining holes and electrons from the hole transport layer and the electron transport layer, respectively, and a material having good quantum efficiency for fluorescence or phosphorescence is preferable. Specific examples include 8-hydroxy-quinoline aluminum complex (Alq ₃ ); carbazole-based compounds; dimerized styryl compounds; BAlq; 10-hydroxybenzo quinoline-metal compounds; compounds of the benzoxazole, benzthiazole and benzimidazole series; Poly(p-phenylenevinylene) (PPV)-based polymers; spiro compounds; polyfluorene, rubrene, and the like, but is not limited thereto.

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

When the emission layer emits red light, the emission dopant is PIQIr(acac)(bis(1-phenylisoquinoline)acetylacetonateiridium), PQIr(acac)(bis(1-phenylquinoline)acetylacetonate iridium), PQIr(tris(1-phenylquinoline)iridium) ), a phosphorescent material such as octaethylporphyrin platinum (PtOEP), or a fluorescent material such as Alq ₃ (tris(8-hydroxyquinolino)aluminum) may be used, but is not limited thereto. When the emission layer emits green light, a phosphor such as Ir(ppy) ₃ (fac tris(2-phenylpyridine)iridium) or a fluorescent material such as Alq3 (tris(8-hydroxyquinolino)aluminum) may be used as the emission dopant. However, the present invention is not limited thereto. When the light emitting layer emits blue light, the light emitting dopant includes a phosphorescent material such as (4,6-F2ppy) ₂ Irpic, spiro-DPVBi, spiro-6P, distylbenzene (DSB), distrylarylene (DSA), A fluorescent material such as a PFO-based polymer or a PPV-based polymer may be used, but is not limited thereto.

A hole blocking layer may be provided between the electron transport layer and the light emitting layer, and a material known in the art may be used.

The electron transport layer may serve to facilitate the transport of electrons. As the electron transport material, a material capable of well injecting electrons from the cathode and transferring them to the light emitting layer, and a material having high electron mobility is suitable. Specific examples include the above-mentioned compound or Al complex of 8-hydroxyquinoline; complexes containing Alq ₃ ; organic radical compounds; hydroxyflavone-metal complexes, and the like, but are not limited thereto. The thickness of the electron transport layer may be 1 to 50 nm. If the thickness of the electron transport layer is 1 nm or more, there is an advantage that the electron transport properties can be prevented from being deteriorated, and if it is 50 nm or less, the thickness of the electron transport layer is too thick to prevent the driving voltage from being raised to improve the movement of electrons. There are advantages that can be

The electron injection layer may serve to facilitate electron injection. The electron injection material has the ability to transport electrons, has an electron injection effect from the cathode, an excellent electron injection effect on the light emitting layer or the light emitting material, prevents the movement of excitons generated in the light emitting layer to the hole injection layer, and also , a compound having excellent thin film forming ability is preferable. Specifically, fluorenone, anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, preorenylidene methane, anthrone, etc., derivatives thereof, metals 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, 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-crezolato)gallium, bis(2-methyl-8-quinolinato)(1-naphtolato)aluminum, bis(2-methyl-8-quinolinato)(2-naphtolato)gallium, etc. However, the present invention is not limited thereto.

The hole blocking layer is a layer that blocks the holes from reaching the cathode, and may be generally formed under the same conditions as the hole injection layer. Specifically, there are oxadiazole derivatives, triazole derivatives, phenanthroline derivatives, BCP, aluminum complex, and the like, but is not limited thereto.

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

Hereinafter, examples will be given to describe the present specification in detail. However, the embodiments according to the present specification may be modified in various other forms, and the scope of the present application is not to be construed as being limited to the embodiments described below. The embodiments of the present application are provided to more completely explain the present specification to those of ordinary skill in the art.

<Synthesis example>

<Synthesis of Compound 1-1>

2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine (20g, 38.88mol), 2-(4-(9,9-dimethyl-9H) -fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (16.95 g, 42.77 mmol), potassium carbonate (10.75 g, 77.76 mmol) aqueous solution was dissolved in 300 mL of Tetrahydrofuran solvent. and increase the temperature. When reflux started, Tetrakis (triphenylphosphine) palladium (0) (1.35 g, 1.17 mmol) was added and stirred for an additional 1 hour. After completion of the reaction, [Compound 1-1] (23 g, yield 84%) was prepared through cooling and purification of an ethanol slurry.

[M + H] ⁺ = 704

<Synthesis of compound 1-2>

(4-(4-(4,6-diphenyl-1,3,5-) instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine triazin-2-yl)phenyl)naphthalen-2-yl)boronic acid was used, and 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5 In the same manner as in the synthesis of [Compound 1-1], [Compound 1- 2] was prepared.

[M + H] ⁺ = 628

<Synthesis of compound 1-3>

4-(4-(4-([1,1'-biphenyl]-3 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine) -yl)-6-phenyl-1,3,5-triazin-2-yl)phenyl)naphthalen-2-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate and 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane instead of (3-(9 [Compound 1-3] was prepared in the same manner as in [Compound 1-1], except that ,9-dimethyl-9H-fluoren-3-yl)phenyl)boronic acid was used.

[M + H] ⁺ = 780

<Synthesis of compound 1-4>

2-(3-(3-bromonaphthalen-1-yl)phenyl)-4 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine; Using 6-diphenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1, Except for using (3-(9,9-di-tert-butyl-9H-fluoren-3-yl)phenyl)boronic acid instead of 3,2-dioxaborolane, the same method as the synthesis method of [Compound 1-1] was followed. [Compound 1-4] was prepared.

[M + H] ⁺ = 788

<Synthesis of compound 1-5>

2-(3-(3-bromonaphthalen-1-yl)phenyl)-4- instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine Using phenyl-6-(4-(pyridin-2-yl)phenyl)-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl) Synthesis of [Compound 1-1], except that (9,9-dimethyl-9H-fluoren-2-yl)boronic acid was used instead of -4,4,5,5-tetramethyl-1,3,2-dioxaborolane [Compound 1-5] was prepared in the same manner as

[M + H] ⁺ = 705

<Synthesis of compound 1-6>

2-(4-(3-bromonaphthalen-1-yl)phenyl)-4- instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine Using (naphthalen-2-yl)-6-phenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4, 2-(4-(9,9-dimethyl-9H-fluoren-1-yl)phenyl)-4,4,5,5-tetramethyl-1,3 instead of 5,5-tetramethyl-1,3,2-dioxaborolane [Compound 1-6] was prepared in the same manner as in the synthesis of [Compound 1-1], except that ,2-dioxaborolane was used.

[M + H] ⁺ = 754

<Synthesis of compound 1-7>

2-(4-(3-bromonaphthalen-1-yl)phenyl)-4 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine; Using 6-dimethyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1, [Compound 1- 7] was prepared.

[M + H] ⁺ = 580

<Synthesis of compound 1-8>

2-(4-(3-bromonaphthalen-1-yl)phenyl)-4 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine; Using 6-di-p-tolyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5- 2-(4-(9,9-dimethyl-9H-fluoren-1-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane instead of tetramethyl-1,3,2-dioxaborolane [Compound 1-8] was prepared in the same manner as in the synthesis of [Compound 1-1], except that

[M + H] ⁺ = 732

<Synthesis of compound 1-9>

2-(3-(3-bromonaphthalen-1-yl)phenyl)-4 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine; Using 6-diphenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1, Except for using (5-(9,9-dimethyl-9H-fluoren-2-yl)pyridin-2-yl)boronic acid instead of 3,2-dioxaborolane, follow the same method as the synthesis method of [Compound 1-1]. [Compound 1-9] was prepared.

[M + H] ⁺ = 705

<Synthesis of compound 1-10>

Instead of 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (3-(7-cyano-9 [Compound 1-10] was prepared in the same manner as in [Compound 1-1], except that ,9-dimethyl-9H-fluoren-2-yl)phenyl)boronic acid was used.

[M + H] ⁺ = 729

<Synthesis of compound 1-11>

2-(9,9-dimethyl- instead of 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 9H-fluoren-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane was used in the same manner as in the synthesis of [Compound 1-1] [Compound 1-11] was prepared.

[M + H] ⁺ = 628

<Synthesis of compound 1-12>

4-(4-(3-bromonaphthalen-1-yl)phenyl)-5- instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine Using methyl-2,6-diphenylpyrimidine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2- [Compound 1-12] was prepared in the same manner as in [Compound 1-1], except that (9,9-dimethyl-9H-fluoren-2-yl)boronic acid was used instead of dioxaborolane.

[M + H] ⁺ = 641

<Synthesis of compound 1-13>

2-(2-(3-bromonaphthalen-1-yl)phenyl)-4 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine; Using 6-diphenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1, [Compound 1-13] was prepared in the same manner as in the synthesis of [Compound 1-1], except that (9,9-dipropyl-9H-fluoren-2-yl)boronic acid was used instead of 3,2-dioxaborolane. .

[M + H] ⁺ = 684

<Synthesis of compound 1-14>

2-(3-(3-bromonaphthalen-1-yl)phenyl)-4 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine; Use 6-diphenylpyrimidine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Except for using (3-(9,9-dimethyl-7-phenyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, [compound [Compound 1-14] was prepared in the same manner as in 1-1].

[M + H] ⁺ = 779

<Synthesis of compound 1-15>

9-(4-(4-(2-bromonaphthalen-1-yl)phenyl) instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine -6-phenyl-1,3,5-triazin-2-yl)-9H-carbazole was used, and 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4, The same method as the synthesis method of [Compound 1-1], except that (9,9-dimethyl-9H-fluoren-2-yl)boronic acid was used instead of 4,5,5-tetramethyl-1,3,2-dioxaborolane [Compound 1-15] was prepared with

[M + H] ⁺ = 717

<Synthesis of compound 1-16>

2-(3-(3-bromonaphthalen-1-yl)phenyl)-4 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine; Using 6-diphenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1, [Compound 1- 16] was prepared.

[M + H] ⁺ = 704

<Synthesis of compound 1-17>

2-(3-(3-chloronaphthalen-1-yl)phenyl)-4- instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine Using (naphthalen-1-yl)-6-phenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4, [Compound 1- [Compound 1-17] was prepared in the same manner as in the synthesis method of 1].

[M + H] ⁺ = 838

<Synthesis of compound 1-18>

2-(3-(3-iodonaphthalen-1-yl)phenyl)-4- instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine Using phenyl-6-(pyridin-4-yl)-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4, Use 2-(9,9-dimethyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane instead of 5,5-tetramethyl-1,3,2-dioxaborolane [Compound 1-18] was prepared in the same manner as in the synthesis of [Compound 1-1], except that it was used.

[M + H] ⁺ = 629

<Synthesis of compound 1-19>

2-(4-(3-bromonaphthalen-1-yl)phenyl)-4- instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine Using (tert-butyl)-6-methyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5, Same as the synthesis method of [Compound 1-1] except that (3-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)boronic acid was used instead of 5-tetramethyl-1,3,2-dioxaborolane [Compound 1-19] was prepared by the method.

[M + H] ⁺ = 622

<Synthesis of compound 1-20>

2-(4-(3-bromonaphthalen-1-yl)phenyl)-4 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine; Using 6-diphenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1, [Compound 1- 20] was prepared.

[M + H] ⁺ = 704

<Synthesis of compound 1-21>

4-(3-(4,6-diphenyl-1,3,5-triazin instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine) -2-yl)phenyl)naphthalen-2-yl trifluoromethanesulfonate was used, and 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl- 3-(9,9-dimethyl-9H-fluoren-2-yl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl instead of 1,3,2-dioxaborolane ) Except for using pyridazine, [Compound 1-21] was prepared in the same way as [Compound 1-1].

[M + H] ⁺ = 706

<Synthesis of compound 1-22>

2-(4-(3-chloronaphthalen-1-yl)phenyl)-4 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine; Using 6-diphenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1, 2-(9,9-dimethyl-7-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9H-fluoren- instead of 3,2-dioxaborolane [Compound 1-22] was prepared in the same manner as in the synthesis of [Compound 1-1], except that 2-yl)pyridine was used.

[M + H] ⁺ = 781

<Synthesis of compound 1-23>

4-(4-(3-bromonaphthalen-1-yl)phenyl)-5- instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine Using methyl-2-(naphthalen-1-yl)-6-phenylpyrimidine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5- Using 4,4,5,5-tetramethyl-2-(spiro[cyclohexane-1,9'-fluoren]-2'-yl)-1,3,2-dioxaborolane instead of tetramethyl-1,3,2-dioxaborolane Except for that, [Compound 1-23] was prepared in the same manner as in the synthesis of [Compound 1-1].

[M + H] ⁺ = 731

<Synthesis of compound 1-24>

2-(4-(3-bromonaphthalen-1-yl)phenyl)-4- instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine Using (dibenzo[b,d]furan-2-yl)-6-phenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl ), except that (9,9-dimethyl-9H-fluoren-2-yl)boronic acid was used instead of )-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, [Compound 1-24] was prepared by the same method as the synthesis method.

[M + H] ⁺ = 718

<Synthesis of compound 1-25>

2-(3'-(3-bromonaphthalen-1-yl)-[1, instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine 1'-biphenyl]-3-yl)-4,6-diphenyl-1,3,5-triazine was used, and 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl) 2-(9,9-dimethyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3 instead of -4,4,5,5-tetramethyl-1,3,2-dioxaborolane [Compound 1-25] was prepared in the same manner as in the synthesis of [Compound 1-1], except that ,2-dioxaborolane was used.

[M + H] ⁺ = 704

<Synthesis of compound 1-26>

2-(3-(3-bromonaphthalen-1-yl)phenyl)-4 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine; Using 6-diphenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1, [Compound 1-1] except that (3-(7,9,9-trimethyl-9H-fluoren-2-yl)phenyl)boronic acid was used instead of 3,2-dioxaborolane 1-26] was prepared.

[M + H] ⁺ = 718

<Synthesis of compound 1-27>

3'-(4-(4-(3-bromonaphthalen-1-yl)phenyl instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine) )-6-phenyl-1,3,5-triazin-2-yl)-[1,1'-biphenyl]-4-carbonitrile was used, and 2-(4-(9,9-dimethyl-9H-fluoren) was used. Except for using (9,9-dimethyl-9H-fluoren-2-yl)boronic acid instead of -2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, [ [Compound 1-27] was prepared in the same manner as in the synthesis of Compound 1-1].

[M + H] ⁺ = 729

<Synthesis of compound 1-28>

2-(3-(3-bromonaphthalen-1-yl)phenyl)-4- instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine (2,6-dimethylpyridin-3-yl)-6-phenyl-1,3,5-triazine is used, and 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)- 2-(4-(9,9-dimethyl-9H-fluoren-1-yl)phenyl)-4,4,5,5-tetramethyl instead of 4,4,5,5-tetramethyl-1,3,2-dioxaborolane [Compound 1-28] was prepared in the same manner as in the synthesis of [Compound 1-1], except that -1,3,2-dioxaborolane was used.

[M + H] ⁺ = 733

<Synthesis of compound 1-29>

2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine instead of 2,4-diphenyl-6-(3-(3-(4,4, 5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-1-yl)phenyl)-1,3,5-triazine was used, and 2-(4-(9,9-dimethyl- 5-(2-bromophenyl)-9,9-dimethyl-3-(trifluoromethyl)-9H instead of 9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane [Compound 1-29] was prepared in the same manner as in the synthesis of [Compound 1-1], except that -fluorene was used.

[M + H] ⁺ = 772

<Synthesis of compound 1-30>

9-(4-(3-(3-bromonaphthalen-1-yl)phenyl) instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine -6-phenyl-1,3,5-triazin-2-yl)-9H-carbazole was used, and 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4, 2-(4-(9,9-dimethyl-9H-fluoren-1-yl)phenyl)-4,4,5,5-tetramethyl-1 instead of 4,5,5-tetramethyl-1,3,2-dioxaborolane [Compound 1-30] was prepared in the same manner as in the synthesis of [Compound 1-1], except that ,3,2-dioxaborolane was used.

[M + H] ⁺ = 793

<Synthesis of compound 1-31>

4-(4-(3-bromonaphthalen-1-yl)phenyl)-2 instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine; Use 5,6-triphenylpyrimidine and replace 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane [Compound 1-31] was prepared in the same manner as in the synthesis of [Compound 1-1], except that (3-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)boronic acid was used.

[M + H] ⁺ = 779

<Synthesis of compound 1-32>

2-(6-(3-bromonaphthalen-1-yl)pyridin-3-yl instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine )-4,6-diphenyl-1,3,5-triazine is used, and 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5- 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane instead of tetramethyl-1,3,2-dioxaborolane [Compound 1-32] was prepared in the same manner as in the synthesis of [Compound 1-1], except that

[M + H] ⁺ = 705

<Synthesis of compound 1-33>

2-(3-(3-bromonaphthalen-1-yl)-5-methylphenyl) instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine Use -4,6-diphenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl -In the same manner as in the synthesis of [Compound 1-1], except that (3-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)boronic acid was used instead of -1,3,2-dioxaborolane [ compound 1-33] was prepared.

[M + H] ⁺ = 718

<Synthesis of compound 1-34>

2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine instead of 2,4-diphenyl-6-(3-(5-(4,4, 5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-1-yl)phenyl)-1,3,5-triazine was used, and 2-(4-(9,9-dimethyl- 3-(4-bromonaphthalen-2-yl)-9,9-dimethyl-9H-fluorene instead of 9H-fluoren-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane [Compound 1-34] was prepared in the same manner as in the synthesis of [Compound 1-1], except that

[M + H] ⁺ = 754

<Synthesis of compound 1-35>

2-(3-(3-bromonaphthalen-1-yl)phenyl)-4- instead of 2-(4-(3-bromonaphthalen-1-yl)phenyl)-4,6-diphenyl-1,3,5-triazine Using (fluoranthen-3-yl)-6-phenyl-1,3,5-triazine, 2-(4-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)-4,4, Synthesis of [Compound 1-1], except that (3-(9,9-dimethyl-9H-fluoren-2-yl)phenyl)boronic acid was used instead of 5,5-tetramethyl-1,3,2-dioxaborolane [Compound 1-35] was prepared in the same manner as

[M + H] ⁺ = 828

<Example 1>

A glass substrate coated with a thin film of indium tin oxide (ITO) to a thickness of 100 nm was placed in distilled water in which detergent was dissolved and washed with ultrasonic waves. In this case, a product manufactured by Fischer Co. was used as the detergent, and distilled water that was secondarily filtered with a filter manufactured by Millipore Co. was used as the distilled water. After washing ITO for 30 minutes, ultrasonic cleaning was performed for 10 minutes by repeating twice with distilled water. After washing with distilled water, ultrasonic washing was performed with a solvent of isopropyl alcohol, acetone, and methanol, and after drying, it was transported to a plasma cleaner. In addition, after cleaning the substrate for 5 minutes using oxygen plasma, the substrate was transported to a vacuum evaporator.

On the thus prepared ITO transparent electrode, the following compound HI-A was thermally vacuum deposited to a thickness of 60 nm to form a hole injection layer.

The following compound HAT was vacuum deposited on the hole injection layer to form a 5 nm thick first hole transport layer, and the following compound HT-A was vacuum deposited on the first hole transport layer to form a 50 nm thick second hole transport layer formed.

Then, compound BH and compound BD were vacuum-deposited on the second hole transport layer in a weight ratio of 25:1 to form a light emitting layer having a thickness of 20 nm.

The [Compound 1-1] and the following compound LiQ were vacuum-deposited in a weight ratio of 1:1 on the emission layer to form an electron transport and injection layer having a thickness of 35 nm.

After depositing lithium fluoride (LiF) to a thickness of 1 nm on the electron transport and injection layer, aluminum was then deposited to a thickness of 100 nm to form a cathode, thereby manufacturing an organic light emitting diode.

In the above process, the deposition rate of organic material was maintained at 0.04 nm/sec to 0.09 nm/sec, the deposition rate of lithium fluoride was maintained at 0.03 nm/sec, and the deposition rate of aluminum was maintained at 0.2 nm/sec. During deposition, the vacuum was maintained between 1Х10 ^-7 torr to 5Х10 ^-5 torr.

<Examples 2-35>

An organic light emitting diode was manufactured in the same manner as in Example 1, except that the compound of Table 1 was used instead of [Compound 1-1] of Example 1.

<Comparative Examples 1 to 11>

An organic light emitting diode was manufactured in the same manner as in Example 1, except that the compound of Table 1 was used instead of [Compound 1-1] of Example 1.

The voltage and efficiency of the organic light emitting devices of Examples 1 to 35 and Comparative Examples 1 to 11 were measured under a current density of 10 mA/cm ² , and the lifetime (LT ₉₅ ) was measured under a current density of 20 mA/cm ² , and the The results are shown in Table 1 below. In this case, LT ₉₅ means the time when the luminance becomes 95% compared to the initial luminance. The color coordinates (x, y) mean CIE color coordinates.

electron transport and injection layer Driving voltage (V) Efficiency (cd/A) Color coordinates (x, y) LT ₉₅ (h) Example 1 compound 1-1 3.87 5.07 (0.142, 0.097) 284 Example 2 compound 1-2 3.90 5.09 (0.142, 0.097) 270 Example 3 compound 1-3 3.93 5.10 (0.142, 0.098) 269 Example 4 compound 1-4 3.96 5.08 (0.142, 0.096) 308 Example 5 compound 1-5 3.95 5.00 (0.142, 0.097) 274 Example 6 compound 1-6 3.96 5.03 (0.142, 0.097) 295 Example 7 compound 1-7 4.05 5.04 (0.142, 0.096) 264 Example 8 compounds 1-8 4.04 5.07 (0.142, 0.096) 279 Example 9 compounds 1-9 4.08 5.15 (0.142, 0.097) 300 Example 10 compounds 1-10 4.11 5.03 (0.142, 0.097) 347 Example 11 compound 1-11 3.86 4.92 (0.142, 0.097) 267 Example 12 compound 1-12 3.98 5.06 (0.142, 0.096) 295 Example 13 compound 1-13 3.92 5.17 (0.142, 0.096) 260 Example 14 compound 1-14 4.06 5.08 (0.142, 0.096) 294 Example 15 compound 1-15 4.14 5.09 (0.142, 0.097) 282 Example 16 compound 1-16 3.94 5.20 (0.142, 0.096) 280 Example 17 compound 1-17 4.05 5.05 (0.142, 0.097) 300 Example 18 compound 1-18 4.02 5.08 (0.142, 0.096) 276 Example 19 compound 1-19 4.06 5.02 (0.142, 0.097) 262 Example 20 compound 1-20 3.93 5.04 (0.142, 0.097) 283 Example 21 compound 1-21 4.04 5.10 (0.142, 0.097) 293 Example 22 compound 1-22 4.03 5.09 (0.142, 0.097) 305 Example 23 compound 1-23 4.02 5.12 (0.142, 0.097) 268 Example 24 compound 1-24 3.98 5.06 (0.142, 0.097) 278 Example 25 compounds 1-25 3.97 5.22 (0.142, 0.097) 264 Example 26 compound 1-26 4.04 5.03 (0.142, 0.097) 281 Example 27 compound 1-27 4.03 5.05 (0.142, 0.097) 340 Example 28 compound 1-28 4.08 5.00 (0.142, 0.097) 292 Example 29 compound 1-29 3.99 5.07 (0.142, 0.097) 258 Example 30 compounds 1-30 4.10 5.11 (0.142, 0.097) 286 Example 31 compound 1-31 4.08 5.04 (0.142, 0.097) 296 Example 32 compound 1-32 4.12 5.01 (0.142, 0.097) 300 Example 33 compound 1-33 4.07 5.05 (0.142, 0.097) 275 Example 34 compound 1-34 4.05 5.04 (0.142, 0.097) 293 Example 35 compound 1-35 3.97 5.08 (0.142, 0.097) 276 Comparative Example 1 compound E1 4.26 4.64 (0.142, 0.095) 168 Comparative Example 2 compound E2 4.29 4.48 (0.142, 0.096) 171 Comparative Example 3 compound E3 4.24 4.70 (0.142, 0.096) 180 Comparative Example 4 compound E4 4.28 4.52 (0.142, 0.096) 211 Comparative Example 5 compound E5 4.27 4.61 (0.142, 0.097) 178 Comparative Example 6 compound E6 4.31 4.54 (0.142, 0.096) 179 Comparative Example 7 compound E7 4.34 4.49 (0.142, 0.095) 166 Comparative Example 8 compound E8 4.25 4.57 (0.142, 0.096) 189 Comparative Example 9 compound E9 4.37 4.52 (0.142, 0.096) 159 Comparative Example 10 compound E10 4.28 4.53 (0.142, 0.095) 160 Comparative Example 11 compound E11 4.32 4.62 (0.142, 0.096) 178

Examples 1 to 35 using the compound represented by Formula 1 of the present invention showed overall excellent results in driving voltage, efficiency, and lifespan characteristics compared to Comparative Examples 1 to 11.

Specifically, Comparative Examples 1 and 2 have a structure in which a fluorene group bonded to naphthalene forms a condensed ring, and Examples 1 to 35 using the present compound in which the fluorene group is not condensed are driven compared to Comparative Examples 1 and 2 It showed excellent results in voltage, efficiency and lifespan characteristics.

Comparative Examples 3 to 11 are compounds in which the position at which the linker is bonded to naphthalene is different from the bonding position of Formula 1 of the present invention. Compared to 3 to 11, the driving voltage, efficiency, and lifespan characteristics were excellent.

Through this, it can be confirmed that when the compound represented by Formula 1 of the present invention is used, the driving voltage, efficiency, and lifespan characteristics of the organic light emitting diode can be improved.

1: Substrate
2: anode
3: hole injection layer
4: first hole transport layer
5: second hole transport layer
6: light emitting layer
7: electron transport and injection layer
8: cathode

Claims (13)

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

In Formula 1,
X1 to X3 are the same as or different from each other, each independently N or CR,
At least two of X1 to X3 are N,
L1 and L2 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted arylene group; Or a substituted or unsubstituted divalent heterocyclic group,
Ar1, Ar2 and R are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; nitrile group; nitro group; hydroxyl group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted aryloxy group; A substituted or unsubstituted alkylthio group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group, or a substituted or unsubstituted ring by combining with an adjacent group,
Ar3 and Ar4 are the same as or different from each other, and are each independently a substituted or unsubstituted alkyl group, or Ar3 and Ar4 are bonded to each other to form a substituted or unsubstituted aliphatic hydrocarbon ring,
R1 to R9 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; nitrile group; nitro group; hydroxyl group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted aryloxy group; A substituted or unsubstituted alkylthio group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group,
a is an integer from 0 to 6, and when a is 2 or more, 2 or more R9 are the same as or different from each other,
m and n are each an integer of 0 to 3, and when m and n are each 2 or more, L1 and L2 of 2 or more are the same as or different from each other,
L2 is connected to R1 to R8, Ar3 or Ar4. The method according to claim 1,
Formula 1 is a compound represented by any one of the following Formulas 1-1 to 1-5:
[Formula 1-1]

[Formula 1-2]

[Formula 1-3]

[Formula 1-4]

[Formula 1-5]

In Formulas 1-1 to 1-5,
Definitions of X1 to X3, L1, L2, Ar1 to Ar4, R1 to R9, a, m, and n are the same as those in Formula 1 above. The method according to claim 1,
Wherein Ar3 and Ar4 are the same as or different from each other, and each independently is an alkyl group having 1 to 10 carbon atoms, or Ar3 and Ar4 are combined with each other to form an aliphatic hydrocarbon ring having 3 to 10 carbon atoms. The method according to claim 1,
Ar1 and Ar2 are the same as or different from each other, and each independently an alkyl group unsubstituted or substituted with a cyano group, an alkyl group, or a heterocyclic group; an aryl group unsubstituted or substituted with a cyano group, an alkyl group, or a heterocyclic group; Or a compound that is a heterocyclic group unsubstituted or substituted with a cyano group, an alkyl group or a heterocyclic group. The method according to claim 1,
The L1 and L2 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted phenylene group; a substituted or unsubstituted biphenylene group; a substituted or unsubstituted naphthylene group; a substituted or unsubstituted divalent pyridine group; A substituted or unsubstituted divalent pyridazine group; Or a compound that is a substituted or unsubstituted divalent quinazoline group. The method according to claim 1,
The compound of Formula 1 is represented by any one of the following compounds:

. anode; cathode; and at least one organic material layer provided between the anode and the cathode, wherein at least one of the organic material layers comprises the compound according to any one of claims 1 to 6. 8. The method of claim 7,
The organic material layer includes an electron transport layer, an electron injection layer, or an electron transport and injection layer, and the electron transport layer, the electron injection layer, or the electron transport and injection layer includes the compound. 9. The method of claim 8,
The electron transport layer, the electron injection layer, or the electron transport and injection layer is an organic light emitting device that further comprises an n-type dopant. 10. The method of claim 9,
The compound and the n-type dopant are included in a weight ratio of 2:8 to 8:2 organic light emitting device. 8. The method of claim 7,
The organic material layer may include a hole blocking layer, and the hole blocking layer may include the compound. 8. The method of claim 7,
The organic material layer includes an emission layer, and the emission layer includes the compound. 8. The method of claim 7,
The organic material layer includes a hole injection layer, a hole transport layer, or a hole injection and transport layer, and the hole injection layer, the hole transport layer, or the hole injection and transport layer is an organic light emitting device that includes the compound.

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