KR102381641B1 - Organic light emitting device - Google Patents

Abstract

The present specification provides an organic light emitting device including a compound represented by Formula 1 and a compound represented by Formula 2;

Description

Organic light emitting device {ORGANIC LIGHT EMITTING DEVICE}

The present specification relates to an organic light emitting device.

This application claims the benefit of the filing date of Korean Patent Application No. 10-2019-0093159 filed with the Korean Intellectual Property Office on July 31, 2019, the entire contents of which are incorporated herein by reference.

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. In the structure of the organic light emitting device, when a voltage is applied between the two electrodes, 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 the excitons 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.

Chinese Patent Publication No. 108137618

The present specification provides an organic light emitting device.

The present specification includes a first electrode; a second electrode; and an organic material layer provided between the first electrode and the second electrode,

The organic material layer provides an organic light emitting device including a first organic material layer including a compound represented by the following formula (1) and a second organic material layer including a compound represented by the following formula (2).

[Formula 1]

In Formula 1,

A1, A2, A3, B1 and B2 are the same as or different from each other, and each independently represent a hydrocarbon ring;

R1 to R5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; nitrile group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted alkynyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; a substituted or unsubstituted aryloxy group; Or a substituted or unsubstituted heterocyclic group; It is represented by the following formula (3),

At least one of R1 to R5 is represented by the following formula (3),

[Formula 3]

The dotted line is a region connected to A1, A2, A3, B1 or B2,

X is C or Si,

R6 to R8 are the same as or different from each other, and are each independently a substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group,

n1 and n5 are each an integer from 0 to 4,

n2 and n4 are each an integer from 0 to 5;

n3 is an integer from 0 to 3,

n1 + n2 + n3 + n4 + n5 is greater than or equal to 1,

When n1 to n5 are 2 or more, the substituents in parentheses are the same as or different from each other,

[Formula 2]

In Formula 2,

At least one of X1 to X3 is N, and the rest are each independently N or CH,

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

Ar5 and Ar6 are the same as or different from each other, and each independently a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group,

Ar7 is a substituted or unsubstituted m-valent aryl group; Or a substituted or unsubstituted m is a cycloalkyl group,

m is an integer of 2 to 4, and when m is 2 or more, two or more substituents in parentheses are the same as or different from each other.

The organic light emitting device described in the present specification includes the compound represented by Formula 1 in the first organic layer, and the compound represented by Formula 2 in the second organic layer, thereby having a low driving voltage, excellent efficiency characteristics, and excellent lifespan. have Specifically, a low driving voltage, high efficiency, and lifespan may be improved by controlling the degree of electron transport through appropriate adjustment of the HOMO energy level and the LUMO energy level.

1, 2 and 8 show examples of an organic light emitting device according to an exemplary embodiment of the present specification.
3 to 7 show examples of organic light emitting devices including two or more stacks.

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

The present specification provides an organic light emitting device including a first organic material layer including a compound represented by Formula 1 and a second organic material layer including a compound represented by Formula 2 at the same time. The light emitting layer containing the compound of Formula 1 has a shallow HOMO level, and the compound of Formula 2 has a deep HOMO and LUMO level, so electrons can be easily transferred to the light emitting layer, thereby exhibiting high efficiency and lifetime.

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

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 다른 치환기 또는 결합부에 결합되는 부위를 의미한다.In this specification, the dotted line or

is another substituent or means a site bonded to the bonding portion.

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

The term “substituted” 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; cyano group (-CN); nitro group; hydroxyl group; silyl group; boron group; an alkyl group; alkenyl group; alkynyl group; alkoxy group; an alkylthio group; aryloxy group; arylthio group; cycloalkyl group; aryl group; amine 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.

또는

의 치환기가 될 수 있다. In the present specification, that two or more substituents are connected means that hydrogen of any one substituent is replaced with another substituent. For example, an isopropyl group and a phenyl group are linked

or

It can be a substituent of

또는

의 치환기가 될 수 있다. 4 이상의 치환기가 연결되는 것에도 전술한 것과 동일하게 적용된다.In the present specification, three substituents are connected to (substituent 1)-(substituent 2)-(substituent 3) as well as consecutively connected (substituent 1) to (substituent 2) and (substituent 3) It also includes connecting. For example, two phenyl groups and an isopropyl group are linked

or

It can be a substituent of The same applies to those in which 4 or more substituents are connected.

In the present specification, "substituted with A or B" includes not only the case substituted with A or only B, but also the case substituted with A and B.

In the present specification, "substituted or unsubstituted" means deuterium; halogen group; cyano group (-CN); nitro group; hydroxyl group; silyl group; boron group; an alkyl group having 1 to 10 carbon atoms; an alkenyl group having 2 to 10 carbon atoms; an alkynyl group having 2 to 10 carbon atoms; an alkoxy group having 1 to 10 carbon atoms; an alkylthio group having 1 to 10 carbon atoms; an aryloxy group having 6 to 30 carbon atoms; an arylthio group having 6 to 30 carbon atoms; a cycloalkyl group having 3 to 30 carbon atoms; an aryl group having 6 to 30 carbon atoms; amine group; And it means that it is substituted with one or more substituents selected from the group consisting of a heterocyclic group having 2 to 30 carbon atoms, or substituted with a substituent to which two or more groups selected from the group are connected, or does not have any substituents.

In the present specification, "substituted or unsubstituted" means deuterium; halogen group; cyano group (-CN); nitro group; hydroxyl group; silyl group; boron group; an alkyl group having 1 to 6 carbon atoms; an alkenyl group having 2 to 6 carbon atoms; an alkynyl group having 2 to 6 carbon atoms; an alkoxy group having 1 to 6 carbon atoms; an alkylthio group having 1 to 6 carbon atoms; an aryloxy group having 6 to 20 carbon atoms; an arylthio group having 6 to 20 carbon atoms; a cycloalkyl group having 3 to 20 carbon atoms; an aryl group having 6 to 20 carbon atoms; amine group; And it means that it is substituted with one or more substituents selected from the group consisting of a heterocyclic group having 2 to 20 carbon atoms, or substituted with a substituent to which two or more groups selected from the group 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 alkyl group includes a straight or branched chain, and the number of carbon atoms is not particularly limited, but is 1 to 60, 1 to 30, or 1 to 20. Specific examples of the alkyl group include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, and the like, and the alkyl group may be a straight chain or a branched chain. The group includes an n-propyl group and an isopropyl group, and the butyl group includes an n-butyl group, an isobutyl group and a tert-butyl group.

In the present specification, the number of carbon atoms of the cycloalkyl group is not particularly limited, but is 3 to 60, 3 to 30, 3 to 20, or 3 to 10. Cycloalkyl groups include not only monocyclic groups, but also bicyclic groups such as bridgeheads, fused rings, and spiro rings. Specifically, there are a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, an adamantyl group, and the like, but is not limited thereto.

In the present specification, the cycloalkene (cycloalkene) has a double bond in the hydrocarbon ring, but as a non-aromatic ring group, the number of carbon atoms is not particularly limited, but 3 to 60, 3 to 30, 3 to 20, or 3 to 10 am. Cycloalkenes include not only monocyclic groups but also bicyclic groups such as bridgeheads, fused rings, and spiro rings. Examples of the cycloalkene include, but are not limited to, cyclopropene, cyclobutene, cyclopentene, and cyclohexene.

In the present specification, an alkoxy group is an aryl group connected to an oxygen atom, an acylthio group is an alkyl group connected to a sulfur atom, and the description regarding the alkyl group described above can be applied to the alkyl group of the alkoxy group and the alkylthio group.

In the present specification, the aryl group may be a monocyclic aryl group or a polycyclic aryl group, and the number of carbon atoms is not particularly limited, but is 6 to 60, 6 to 30, or 6 to 20. The monocyclic aryl group may be a phenyl group, a biphenyl group, a terphenyl group, a quaterphenyl group, and the like, 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, fluoranthenyl group, triphenylenyl group, etc. , but is not limited thereto.

In the present specification, the 9th carbon atom (C) of the fluorenyl group may be substituted with an alkyl group, an aryl group, or the like, and two substituents may be bonded to each other to form a spiro structure such as cyclopentane or fluorene.

In the present specification, the substituted aryl group may include a form in which an aliphatic ring is condensed to an aryl group. For example, a tetrahydronaphthalene group of the following structure is included in a substituted aryl group. In the following structure, one of the carbons of the benzene ring may be connected to another position.

In the present specification, an aryloxy group is an aryl group connected to an oxygen atom, an arylthio group is an aryl group connected to a sulfur atom, and the description regarding the aryl group described above can be applied to the aryl group of the aryloxy group and the arylthio group. The aryl group of the aryloxy group is the same as the example of the aryl group described above. Specifically, the aryloxy group includes a phenoxy group, p-tolyloxy group, m-tolyloxy group, 3,5-dimethyl-phenoxy group, 2,4,6-trimethylphenoxy group, p-tert-butylphenoxy group, 3- Biphenyloxy group, 4-biphenyloxy group, 1-naphthyloxy group, 2-naphthyloxy group, 4-methyl-1-naphthyloxy group, 5-methyl-2-naphthyloxy group, 1-anthryloxy group , 2-anthryloxy group, 9-anthryloxy group, 1-phenanthryloxy group, 3-phenanthryloxy group, 9-phenanthryloxy group, and the like, and the arylthioxy group includes phenylthioxy group, 2- and a methylphenylthioxy group, a 4-tert-butylphenylthioxy group, and the like, but are not limited thereto.

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; a substituted or unsubstituted cycloalkyl group; Or it may be a substituted or unsubstituted aryl group. The silyl group is specifically trimethylsilyl group, triethylsilyl group, tert-butyldimethylsilyl group, vinyldimethylsilyl group, propyldimethylsilyl group, dimethylphenylsilyl group, triphenylsilyl group, diphenylsilyl group, phenylsilyl group, etc. but is not limited thereto.

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; a substituted or unsubstituted cycloalkyl group; Or it may be a substituted or unsubstituted aryl group. The silyl group specifically includes, but is not limited to, a dimethyl boron group, a diethyl boron group, a tert-butylmethyl boron group, a vinyl methyl boron group, a propylmethyl boron group, a methylphenyl boron group, a diphenyl boron group, a phenyl boron group, and the like. .

In the present specification, the amine group may be represented by -NRaRb, wherein Ra and Rb are each hydrogen; a substituted or unsubstituted alkyl group; a substituted or unsubstituted aryl group; Or it may be a substituted or unsubstituted heteroaryl group, but is not limited thereto. The amine group is selected from the group consisting of an alkylamine group, an alkylarylamine group, an arylamine group, a heteroarylamine group, an alkylheteroarylamine group, and an arylheteroarylamine group, depending on the type of the substituent (Ra, Rb) to be bonded. can be

In the present specification, the alkylamine group refers to an amine group substituted with an alkyl group, and the number of carbon atoms is not particularly limited, but may be 1 to 40 or 1 to 20. Specific examples of the alkylamine group include, but are not limited to, a methylamine group, a dimethylamine group, an ethylamine group, and a diethylamine group.

In the present specification, examples of the arylamine group include a substituted or unsubstituted monoarylamine group, a substituted or unsubstituted diarylamine group, or a substituted or unsubstituted arylheteroarylamine group. The aryl group in the arylamine group may be a monocyclic or polycyclic aryl group. Specific examples of the arylamine group include a phenylamine group, a naphthylamine group, a biphenylamine group, an anthracenylamine group, a diphenylamine group, a phenylnaphthylamine group, and a bis(tert-butylphenyl)amine group. , but is not limited thereto.

In the present specification, examples of the heteroarylamine group include a substituted or unsubstituted monoheteroarylamine group, a substituted or unsubstituted diheteroarylamine group, or a substituted or unsubstituted arylheteroarylamine group.

In the present specification, the arylheteroarylamine group means an amine group substituted with an aryl group and a heteroaryl group, and the description of the above-described aryl group and the heteroaryl group to be described later may be applied.

In the present specification, the heterocyclic group is a ring group including at least one of N, O, S, and Si as a heteroatom, and the number of carbon atoms is not particularly limited, but is 2 to 60, or 2 to 30. Examples of the heterocyclic group include, but are not limited to, a pyridyl group; quinoline group; thiophene group; dibenzothiophene group; furan group; dibenzofuran group; naphthobenzofuran group; a carbazole group; benzocarbazole group; naphthobenzothiophene group; hexahydrocarbazole group; dihydroacridine group; dihydrodibenzoazacillin group; phenoxazine; phenothiazine; dihydrodibenzoazacillin group; spiro (dibenzosilol-dibenzoazacillin) groups; spiro (acridine-fluorene) group; spiro (fluorene-xanthene) group; Spiro (fluorene-thioxanthene) and the like, but is 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.

As used herein, “adjacent” The group may mean a substituent substituted on an atom directly connected to the atom in which the substituent is substituted, a substituent positioned sterically close to the substituent, or another substituent substituted on the atom in which the substituent is substituted.

In the present specification, "a ring formed by bonding adjacent groups" is a hydrocarbon ring; or a heterocyclic ring.

In the present specification, "a 5-membered or 6-membered ring formed by bonding adjacent groups" means that the ring including the substituents participating in the ring formation is 5-membered or 6-membered. It may include condensing an additional ring to a ring including a substituent participating in the ring formation.

In the present specification, the hydrocarbon ring may be an aromatic, aliphatic, or a condensed ring of aromatic and aliphatic, and the description of the aryl group described above may be applied except that the aromatic hydrocarbon ring is not monovalent, and the aliphatic hydrocarbon ring is Except for the non-monovalent, the above description of the cycloalkyl group may be applied. Examples of the condensed ring of the aromatic and the aliphatic include a 1,2,3,4-tetrahydronaphthalene group, a 2,3-dihydro-1H-indene group, and the like, but are not limited thereto.

In the present specification, the description of the heterocyclic group may be applied except that the heterocycle is not monovalent.

In the present specification, the aromatic hydrocarbon ring refers to a ring in which pi electrons are completely conjugated and planar, and the description of the aryl group described above may be applied, except that it is a divalent group.

In the present specification, the aliphatic hydrocarbon ring refers to all hydrocarbon rings except for the aromatic hydrocarbon ring, and may include a cycloalkyl ring. Except that the cycloalkyl ring is a divalent group, the description of the cycloalkyl group described above may be applied. The substituted aliphatic hydrocarbon ring also includes an aliphatic hydrocarbon ring in which an aromatic ring is condensed.

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

In the present specification, the description of the above-described cycloalkyl group may be applied except that the cycloalkylene group is a divalent group.

Hereinafter, Formula 1 will be described.

[Formula 1]

In an exemplary embodiment of the present specification, A1 to A3, B1 and B2 are the same as or different from each other, and each independently represent a monocyclic or bicyclic hydrocarbon ring.

In an exemplary embodiment of the present specification, A1 to A3, B1 and B2 are the same as or different from each other, and each independently represents a benzene ring or a naphthalene ring.

In an exemplary embodiment of the present specification, A1 to A3 are each a benzene ring.

In an exemplary embodiment of the present specification, B1 and B2 are each a benzene ring.

In the exemplary embodiment of the present specification, Chemical Formula 1 is represented by the following Chemical Formula 1-1.

[Formula 1-1]

In Formula 1-1, R1 to R5 and n1 to n5 are as defined in Formula 1 above.

In an exemplary embodiment of the present specification, R1 to R5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; cyano group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted alkynyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; a substituted or unsubstituted aryloxy group; Or a substituted or unsubstituted heterocyclic group, or represented by the above formula (3).

In an exemplary embodiment of the present specification, R1, R2, R4, and R5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; cyano group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; a substituted or unsubstituted heterocyclic group; Or represented by the above formula (3).

In an exemplary embodiment of the present specification, R1, R2, R4, and R5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; cyano group; a substituted or unsubstituted C 1 to C 10 alkyl group; a substituted or unsubstituted C 3 to C 30 cycloalkyl group; a substituted or unsubstituted C1-C30 alkylsilyl group; a substituted or unsubstituted C6-C90 arylsilyl group; a substituted or unsubstituted C1-C20 alkylamine group; a substituted or unsubstituted C6-C60 arylamine group; a substituted or unsubstituted heteroarylamine group having 2 to 60 carbon atoms; a substituted or unsubstituted C6-C30 aryl group; a substituted or unsubstituted heterocyclic group having 2 to 30 carbon atoms; Or represented by the above formula (3).

In an exemplary embodiment of the present specification, R1, R2, R4, and R5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; cyano group; a substituted or unsubstituted C 1 to C 6 alkyl group; a substituted or unsubstituted 3 to 20 cycloalkyl group; a substituted or unsubstituted C 1 to C 18 alkylsilyl group; a substituted or unsubstituted C6-C60 arylsilyl group; a substituted or unsubstituted C1-C12 alkylamine group; a substituted or unsubstituted C6-C40 arylamine group; a substituted or unsubstituted C 2 to C 40 heteroarylamine group; a substituted or unsubstituted C6-C20 aryl group; a substituted or unsubstituted heterocyclic group having 2 to 20 carbon atoms; Or represented by the above formula (3).

In an exemplary embodiment of the present specification, R1, R2, R4, and R5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; cyano group; an alkyl group having 1 to 10 carbon atoms that is unsubstituted or substituted with deuterium; a cycloalkyl group having 3 to 30 carbon atoms that is unsubstituted or substituted with deuterium; an arylamine group having 6 to 60 carbon atoms that is unsubstituted or substituted with deuterium; an aryl group having 6 to 30 carbon atoms which is unsubstituted or substituted with one or more substituents selected from the group consisting of deuterium, a halogen group, a cyano group and an alkyl group having 1 to 10 carbon atoms, or a substituent to which two or more groups selected from the group are connected; a heterocyclic group having 2 to 30 carbon atoms that is unsubstituted or substituted with deuterium; Or represented by the above formula (3).

In an exemplary embodiment of the present specification, R1, R2, R4, and R5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; cyano group; a C 1 to C 6 alkyl group unsubstituted or substituted with deuterium; a cycloalkyl group having 3 to 20 carbon atoms that is unsubstituted or substituted with deuterium; an arylamine group having 6 to 40 carbon atoms that is unsubstituted or substituted with deuterium; A C 6 to C 20 aryl group unsubstituted or substituted with one or more substituents selected from the group consisting of deuterium, a halogen group, a cyano group, and an alkyl group having 1 to 6 carbon atoms, or a substituent to which two or more groups selected from the group are connected; a heterocyclic group having 2 to 20 carbon atoms that is unsubstituted or substituted with deuterium; Or represented by the above formula (3).

In an exemplary embodiment of the present specification, R1, R2, R4, and R5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; a cyano group' an alkyl group having 1 to 6 carbon atoms that is unsubstituted or substituted with deuterium; a cycloalkyl group having 3 to 20 carbon atoms; an arylamine group having 6 to 40 carbon atoms; a C6-C20 aryl group unsubstituted or substituted with deuterium, a halogen group, a nitrile group, a C1-C6 alkyl group, or a C1-C6 alkyl group substituted with deuterium; a heterocyclic group having 2 to 20 carbon atoms; Or represented by the above formula (3).

In one embodiment of the present specification, the heterocyclic group of R1, R2, R4 and R5 includes N as a heterogeneous element.

In an exemplary embodiment of the present specification, R1, R2, R4, and R5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; fluoro group; cyano group; a methyl group unsubstituted or substituted with deuterium; isopropyl group; tert-butyl group; cyclohexyl group; diphenylamine group; a phenyl group unsubstituted or substituted with deuterium, a fluoro group, a cyano group, a tert-butyl group, or CD ₃ ; biphenyl group; naphthyl group; or a pyridine group.

In an exemplary embodiment of the present specification, R3 is hydrogen; heavy hydrogen; halogen group; nitrile group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted alkynyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; a substituted or unsubstituted aryloxy group; Or a substituted or unsubstituted heterocyclic group; It is represented by the following formula (3).

In an exemplary embodiment of the present specification, R3 is hydrogen; heavy hydrogen; halogen group; cyano group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; a substituted or unsubstituted heterocyclic group; Or represented by the above formula (3).

In an exemplary embodiment of the present specification, R3 is hydrogen; heavy hydrogen; halogen group; cyano group; a substituted or unsubstituted C 1 to C 10 alkyl group; a substituted or unsubstituted C 3 to C 30 cycloalkyl group; a substituted or unsubstituted C1-C30 alkylsilyl group; a substituted or unsubstituted C6-C90 arylsilyl group; a substituted or unsubstituted C1-C20 alkylamine group; a substituted or unsubstituted C6-C60 arylamine group; a substituted or unsubstituted heteroarylamine group having 2 to 60 carbon atoms; a substituted or unsubstituted C6-C30 aryl group; a substituted or unsubstituted heterocyclic group having 2 to 30 carbon atoms; Or represented by the above formula (3).

In an exemplary embodiment of the present specification, R3 is hydrogen; heavy hydrogen; halogen group; cyano group; a substituted or unsubstituted C 1 to C 6 alkyl group; a substituted or unsubstituted 3 to 20 cycloalkyl group; a substituted or unsubstituted C 1 to C 18 alkylsilyl group; a substituted or unsubstituted C6-C60 arylsilyl group; a substituted or unsubstituted C1-C12 alkylamine group; a substituted or unsubstituted C6-C40 arylamine group; a substituted or unsubstituted C 2 to C 40 heteroarylamine group; a substituted or unsubstituted C6-C20 aryl group; a substituted or unsubstituted heterocyclic group having 2 to 20 carbon atoms; Or represented by the above formula (3).

In an exemplary embodiment of the present specification, R3 is hydrogen; heavy hydrogen; halogen group; cyano group; an alkyl group having 1 to 10 carbon atoms that is unsubstituted or substituted with deuterium; a cycloalkyl group having 3 to 30 carbon atoms that is unsubstituted or substituted with deuterium; At least one substituent selected from the group consisting of deuterium, a halogen group, a cyano group, an alkyl group having 1 to 10 carbon atoms, an aryl group having 6 to 30 carbon atoms, and a silyl group, or a substituent selected from the group consisting of two or more groups selected from the group consisting of a substituted or unsubstituted C6 to 60 arylamine groups; an aryl group having 6 to 30 carbon atoms that is unsubstituted or substituted with deuterium, a halogen group, or a cyano group; a heterocyclic group having 2 to 30 carbon atoms that is unsubstituted or substituted with deuterium; Or represented by the above formula (3).

In an exemplary embodiment of the present specification, R3 is hydrogen; heavy hydrogen; halogen group; cyano group; a C 1 to C 6 alkyl group unsubstituted or substituted with deuterium; a cycloalkyl group having 3 to 20 carbon atoms that is unsubstituted or substituted with deuterium; At least one substituent selected from the group consisting of deuterium, a halogen group, a cyano group, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 20 carbon atoms, and a silyl group, or a substituent selected from the group consisting of two or more groups selected from the group consisting of a substituted or unsubstituted C6 to 40 arylamine groups; an aryl group having 6 to 20 carbon atoms unsubstituted or substituted with deuterium, a halogen group, or a cyano group; a heterocyclic group having 2 to 20 carbon atoms that is unsubstituted or substituted with deuterium; Or represented by the above formula (3).

In an exemplary embodiment of the present specification, R3 is hydrogen; heavy hydrogen; halogen group; cyano group; a C 1 to C 6 alkyl group unsubstituted or substituted with deuterium; a cycloalkyl group having 3 to 20 carbon atoms; an arylamine group having 6 to 40 carbon atoms that is unsubstituted or substituted with deuterium, an alkyl group having 1 to 6 carbon atoms, a trialkylsilyl group having 3 to 18 carbon atoms, or a triarylamine group having 18 to 60 carbon atoms; an aryl group having 6 to 20 carbon atoms unsubstituted or substituted with deuterium, a halogen group, or a cyano group; a heterocyclic group having 2 to 20 carbon atoms; Or represented by the above formula (3).

In an exemplary embodiment of the present specification, the heterocyclic group of R3 includes N as a heterogeneous element.

In an exemplary embodiment of the present specification, R3 is hydrogen; heavy hydrogen; a methyl group unsubstituted or substituted with deuterium; tert-butyl group; a diphenylamine group unsubstituted or substituted with deuterium, a tert-butyl group, a trimethylsilyl group, or a triphenylsilyl group; a phenyl group unsubstituted or substituted with deuterium or a fluoro group; or a carbazole group.

In an exemplary embodiment of the present specification, R1, R2, R4, and R5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; cyano group; an alkyl group having 1 to 10 carbon atoms that is unsubstituted or substituted with deuterium; a cycloalkyl group having 3 to 30 carbon atoms that is unsubstituted or substituted with deuterium; an arylamine group having 6 to 60 carbon atoms that is unsubstituted or substituted with deuterium; an aryl group having 6 to 30 carbon atoms, unsubstituted or substituted with one or more substituents selected from the group consisting of deuterium, a halogen group, a cyano group, and an alkyl group having 1 to 10 carbon atoms, or a substituent to which two or more groups selected from the group are connected; a heterocyclic group having 2 to 30 carbon atoms that is unsubstituted or substituted with deuterium; Or represented by the above formula (3),

R3 is hydrogen; heavy hydrogen; halogen group; cyano group; an alkyl group having 1 to 10 carbon atoms that is unsubstituted or substituted with deuterium; a cycloalkyl group having 3 to 30 carbon atoms that is unsubstituted or substituted with deuterium; At least one substituent selected from the group consisting of deuterium, a halogen group, a cyano group, an alkyl group having 1 to 10 carbon atoms, an aryl group having 6 to 30 carbon atoms, and a silyl group, or a substituent selected from the group consisting of two or more groups selected from the group consisting of a substituted or unsubstituted C6 to 60 arylamine groups; an aryl group having 6 to 30 carbon atoms that is unsubstituted or substituted with deuterium, a halogen group, or a cyano group; a heterocyclic group having 2 to 30 carbon atoms that is unsubstituted or substituted with deuterium; Or represented by the above formula (3).

In one embodiment of the present specification, one of R2 is connected to a site in an ortho orientation with respect to the N to which B2 is connected.

In one embodiment of the present specification, one of R4 is connected to a site in an ortho orientation with respect to the N to which B2 is connected.

In one embodiment of the present specification, n1 is 1 or 2.

In an exemplary embodiment of the present specification, n2 is 1 to 4. In another exemplary embodiment, n2 is 1 to 3.

In one embodiment of the present specification, n3 is 1 or 2.

In an exemplary embodiment of the present specification, n4 is 1 to 4. In another exemplary embodiment, n4 is 1 to 3.

In an exemplary embodiment of the present specification, n5 is 1.

In an exemplary embodiment of the present specification, at least one of R1 to R5 is represented by Formula 3 above.

In an exemplary embodiment of the present specification, one to four of R1 to R5 are represented by Formula 3 above.

In an exemplary embodiment of the present specification, one or two of R1 to R5 are represented by Formula 3 above.

In an exemplary embodiment of the present specification, one to four of R1, R2, R4, and R5 are represented by Formula 3 above.

In an exemplary embodiment of the present specification, one or two of R1, R2, R4 and R5 is represented by Formula 3 above.

In an exemplary embodiment of the present specification, R1 is represented by Formula 3 above.

In an exemplary embodiment of the present specification, R2 is represented by Formula 3 above.

In an exemplary embodiment of the present specification, R3 is represented by Formula 3 above.

In an exemplary embodiment of the present specification, R4 is represented by Formula 3 above.

In an exemplary embodiment of the present specification, R5 is represented by Formula 3 above.

In an exemplary embodiment of the present specification, R6 to R8 are the same as or different from each other, and each independently a substituted or unsubstituted C 1 to C 10 alkyl group; or a substituted or unsubstituted C6-C30 aryl group.

In an exemplary embodiment of the present specification, R6 to R8 are the same as or different from each other, and each independently a substituted or unsubstituted C 1 to C 6 alkyl group; or a substituted or unsubstituted C6-C20 aryl group.

In an exemplary embodiment of the present specification, R6 to R8 are the same as or different from each other, and each independently an alkyl group having 1 to 10 carbon atoms substituted or unsubstituted with deuterium; or one or more substituents selected from the group consisting of deuterium, a halogen group, a cyano group, an alkyl group having 1 to 10 carbon atoms, an aryl group having 6 to 30 carbon atoms, and a silyl group, or a substituent selected from the group consisting of two or more groups selected from the group consisting of substituted or unsubstituted carbon atoms It is an aryl group of 6 to 30.

In an exemplary embodiment of the present specification, R6 to R8 are the same as or different from each other, and each independently an alkyl group having 1 to 6 carbon atoms unsubstituted or substituted with deuterium; or one or more substituents selected from the group consisting of deuterium, a halogen group, a cyano group, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 20 carbon atoms, and a silyl group, or a substituent selected from the group consisting of two or more groups selected from the group consisting of a substituted or unsubstituted carbon number 6 to 20 aryl groups.

In an exemplary embodiment of the present specification, R6 to R8 are the same as or different from each other, and each independently an alkyl group having 1 to 6 carbon atoms unsubstituted or substituted with deuterium; Or a C 6 to C 20 aryl group unsubstituted or substituted with a deuterium, a halogen group, a cyano group, an alkyl group having 1 to 6 carbon atoms, an alkyl group having 1 to 6 carbon atoms substituted with deuterium, or a trialkylsilyl group having 3 to 18 carbon atoms .

In an exemplary embodiment of the present specification, R6 to R8 are the same as or different from each other, and each independently a methyl group; tert-butyl group; or a phenyl group unsubstituted or substituted with deuterium, a fluoro group, a methyl group, a tert-butyl group, CD ₃ , or a trimethylsilyl group.

In an exemplary embodiment of the present specification, X is C, and at least one of R6 to R8 is a substituted or unsubstituted alkyl group.

In an exemplary embodiment of the present specification, X is C, and at least two of R6 to R8 are substituted or unsubstituted alkyl groups.

In an exemplary embodiment of the present specification, X is C, and at least one of R6 to R8 is a substituted or unsubstituted aryl group.

In an exemplary embodiment of the present specification, X is C, R6 and R7 are the same as or different from each other, and each independently represents a substituted or unsubstituted alkyl group, and R8 is a substituted or unsubstituted aryl group.

In an exemplary embodiment of the present specification, X is Si, and at least one of R6 to R8 is a substituted or unsubstituted aryl group.

In an exemplary embodiment of the present specification, X is Si, and at least two of R6 to R8 are substituted or unsubstituted aryl groups.

In an exemplary embodiment of the present specification, X is C, R6 and R7 are the same as or different from each other, and each independently represents a substituted or unsubstituted aryl group, and R8 is a substituted or unsubstituted alkyl group.

In an exemplary embodiment of the present specification, X is Si, R6 to R8 are the same as or different from each other, and each independently represents a substituted or unsubstituted aryl group.

In the exemplary embodiment of the present specification, Chemical Formula 3 is represented by the following Chemical Formula 3-1 or 3-2.

[Formula 3-1]

[Formula 3-2]

In Formulas 3-1 and 3-2,

R11 is a substituted or unsubstituted alkyl group,

R12 is a substituted or unsubstituted aryl group,

R13 to R16 are the same as or different from each other, and are each independently a substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group.

In an exemplary embodiment of the present specification, the descriptions of R6 to R8 described above may be applied to R11 to R16.

In an exemplary embodiment of the present specification, R11 is a substituted or unsubstituted C1-C10 alkyl group.

In an exemplary embodiment of the present specification, R11 is a substituted or unsubstituted C 1 to C 6 alkyl group.

In an exemplary embodiment of the present specification, R11 is an alkyl group having 1 to 6 carbon atoms which is unsubstituted or substituted with deuterium.

In an exemplary embodiment of the present specification, R11 is a methyl group.

In an exemplary embodiment of the present specification, R12 is a substituted or unsubstituted C6-C30 aryl group.

In an exemplary embodiment of the present specification, R12 is a substituted or unsubstituted C6-C20 aryl group.

In an exemplary embodiment of the present specification, R12 is one or more substituents selected from the group consisting of deuterium, a halogen group, a cyano group, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 20 carbon atoms, and a silyl group, or two or more selected from the group It is an aryl group having 6 to 20 carbon atoms which is unsubstituted or substituted with a substituent to which the group is connected.

In an exemplary embodiment of the present specification, R12 is deuterium, a halogen group, a cyano group, an alkyl group having 1 to 6 carbon atoms, an alkyl group having 1 to 6 carbon atoms substituted with deuterium, or a trialkylsilyl group having 3 to 18 carbon atoms substituted or unsubstituted It is a cyclic aryl group having 6 to 20 carbon atoms.

In an exemplary embodiment of the present specification, R12 is a phenyl group unsubstituted or substituted with deuterium, a fluoro group, a methyl group, a tert-butyl group, CD ₃ , or a trimethylsilyl group.

In an exemplary embodiment of the present specification, R13 to R16 are the same as or different from each other, and each independently a substituted or unsubstituted C 1 to C 10 alkyl group; or a substituted or unsubstituted C6-C30 aryl group.

In an exemplary embodiment of the present specification, R13 to R16 are the same as or different from each other, and each independently a substituted or unsubstituted C 1 to C 6 alkyl group; or a substituted or unsubstituted C6-C20 aryl group.

In an exemplary embodiment of the present specification, R13 to R16 are the same as or different from each other, and each independently an alkyl group having 1 to 6 carbon atoms unsubstituted or substituted with deuterium; or one or more substituents selected from the group consisting of deuterium, a halogen group, a cyano group, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 20 carbon atoms, and a silyl group, or a substituent group selected from the group consisting of two or more groups selected from the group consisting of substituted or unsubstituted carbon atoms 6 to 20 aryl groups.

In an exemplary embodiment of the present specification, R13 to R16 are the same as or different from each other, and each independently a methyl group; tert-butyl group; or a phenyl group unsubstituted or substituted with deuterium, a fluoro group, a methyl group, a tert-butyl group, CD ₃ , or a trimethylsilyl group.

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

Hereinafter, Formula 2 will be described.

[Formula 2]

According to an exemplary embodiment of the present specification, m is 2.

In an exemplary embodiment of the present specification, Chemical Formula 2 is represented by the following Chemical Formula 2-1.

[Formula 2-1]

In Formula 2-1,

X1 to X3, L, Ar5 and Ar6 are the same as in Formula 2,

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

At least one of X1' to X3' is N, and the rest are each independently N or CH,

Ar5' and Ar6' are the same as or different from each other, and are each independently a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group,

Ar7' is a substituted or unsubstituted arylene group; or a substituted or unsubstituted cycloalkylene group.

According to an exemplary embodiment of the present specification, L' is the same as the definition of L.

According to an exemplary embodiment of the present specification, X1' to X3' are the same as the definitions of X1 to X3.

According to an exemplary embodiment of the present specification, Ar5' and Ar6' are the same as the definitions of Ar5 and Ar6.

According to an exemplary embodiment of the present specification, at least one of X1 to X3 is N, and the rest are each independently N or CH.

In another exemplary embodiment, 2 or 3 of X1 to X3 is N, and the remainder is CH.

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

In another embodiment, X1 and X3 are N, and X2 is CH.

In another embodiment, X2 and X3 are N, and X1 is CH.

In another exemplary embodiment, X1 to X3 are N.

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

In another embodiment, X1' and X3' are N, and X2' is CH.

In another embodiment, X2' and X3' are N, and X1' is CH.

In another exemplary embodiment, X1' to X3' are N.

According to an exemplary embodiment of the present specification, L is a direct bond; or a substituted or unsubstituted arylene group having 6 to 60 carbon atoms.

In another embodiment, L is a direct bond; or a substituted or unsubstituted arylene group having 6 to 30 carbon atoms.

In another embodiment, L is a direct bond; or a substituted or unsubstituted C6-C20 arylene group.

In another embodiment, L is a direct bond; a substituted or unsubstituted phenylene group; Or a substituted or unsubstituted biphenylene group.

According to another embodiment, L is a direct bond; or a phenylene group.

According to an exemplary embodiment of the present specification, L' is a direct bond; or a substituted or unsubstituted arylene group having 6 to 60 carbon atoms.

In another embodiment, L' is a direct bond; or a substituted or unsubstituted arylene group having 6 to 30 carbon atoms.

In another embodiment, L' is a direct bond; or a substituted or unsubstituted C6-C20 arylene group.

In another embodiment, L' is a direct bond; a substituted or unsubstituted phenylene group; Or a substituted or unsubstituted biphenylene group.

According to another embodiment, L' is a direct bond; or a phenylene group.

In an exemplary embodiment of the present specification, L and L' are the same as or different from each other.

In one embodiment of the present specification, L and L' are the same as or different from each other, and each independently a direct bond; or any one selected from the following structures.

In an exemplary embodiment of the present specification, Ar5 and Ar6 are the same as or different from each other, and each independently a substituted or unsubstituted C6-C60 aryl group; Or a substituted or unsubstituted heterocyclic group having 2 to 60 carbon atoms.

In another exemplary embodiment, Ar5 and Ar6 are the same as or different from each other, and each independently a substituted or unsubstituted C6-C30 aryl group; Or a substituted or unsubstituted heterocyclic group having 2 to 30 carbon atoms.

In another exemplary embodiment, Ar5 and Ar6 are the same as or different from each other, and each independently an aryl group having 6 to 30 carbon atoms; or a heterocyclic group having 2 to 30 carbon atoms, and the aryl group or heterocyclic group is one or more substituents selected from the group consisting of deuterium, a halogen group, an alkyl group having 1 to 10 carbon atoms, and an alkoxy group having 1 to 10 carbon atoms, or 2 selected from the group It is substituted or unsubstituted with a substituent to which the above groups are connected.

In another exemplary embodiment, Ar5 and Ar6 are the same as or different from each other, and each independently an aryl group having 6 to 20 carbon atoms; or a heterocyclic group having 2 to 20 carbon atoms, and the aryl group or heterocyclic group is one or more substituents selected from the group consisting of deuterium, a halogen group, an alkyl group having 1 to 6 carbon atoms, and an alkoxy group having 1 to 6 carbon atoms, or 2 selected from the group It is substituted or unsubstituted with a substituent to which the above groups are connected.

In another exemplary embodiment, Ar5 and Ar6 are the same as or different from each other, and each independently substituted or unsubstituted with a halogen group, an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, or a haloalkyl group having 1 to 10 carbon atoms. a cyclic aryl group having 6 to 30 carbon atoms; or a heterocyclic group having 2 to 30 carbon atoms.

In another embodiment, Ar5 and Ar6 are the same as or different from each other, and each independently substituted or unsubstituted with a halogen group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a haloalkyl group having 1 to 6 carbon atoms. a cyclic aryl group having 6 to 20 carbon atoms; or a heterocyclic group having 2 to 20 carbon atoms.

In an exemplary embodiment of the present specification, the heterocyclic group of Ar5 and Ar6 includes N, O, or S as a heterogeneous element. Preferably it contains N.

In another embodiment, Ar5 and Ar6 are the same as or different from each other, and each independently a phenyl group unsubstituted or substituted with a halogen group, a methyl group, a methoxy group, or a trifluoromethyl group; biphenyl group; naphthyl group; thiophene group; or a pyridine group.

In another embodiment, Ar5 and Ar6 are the same as or different from each other, and each independently a phenyl group unsubstituted or substituted with a methyl group; naphthyl group; or a pyridine group.

In an exemplary embodiment of the present specification, Ar5' and Ar6' are the same as or different from each other, and each independently 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 another embodiment, Ar5' and Ar6' are the same as or different from each other, and each independently a substituted or unsubstituted C6-C30 aryl group; Or a substituted or unsubstituted heterocyclic group having 2 to 30 carbon atoms.

In another exemplary embodiment, Ar5' and Ar6' are the same as or different from each other, and each independently an aryl group having 6 to 30 carbon atoms; or a heterocyclic group having 2 to 30 carbon atoms, and the aryl group or heterocyclic group is one or more substituents selected from the group consisting of deuterium, a halogen group, an alkyl group having 1 to 10 carbon atoms, and an alkoxy group having 1 to 10 carbon atoms, or 2 selected from the group It is substituted or unsubstituted with a substituent to which the above groups are connected.

In another embodiment, Ar5' and Ar6' are the same as or different from each other, and each independently an aryl group having 6 to 20 carbon atoms; or a heterocyclic group having 2 to 20 carbon atoms, and the aryl group or heterocyclic group is one or more substituents selected from the group consisting of deuterium, a halogen group, an alkyl group having 1 to 6 carbon atoms, and an alkoxy group having 1 to 6 carbon atoms, or 2 selected from the group It is substituted or unsubstituted with a substituent to which the above groups are connected.

In another embodiment, Ar5' and Ar6' are the same as or different from each other, and are each independently substituted with a halogen group, an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, or a haloalkyl group having 1 to 10 carbon atoms. or an unsubstituted aryl group having 6 to 30 carbon atoms; or a heterocyclic group having 2 to 30 carbon atoms.

In another exemplary embodiment, Ar5' and Ar6' are the same as or different from each other, and are each independently substituted with a halogen group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a haloalkyl group having 1 to 6 carbon atoms. or an unsubstituted C6-C20 aryl group; or a heterocyclic group having 2 to 20 carbon atoms.

In an exemplary embodiment of the present specification, the heterocyclic group of Ar5' and Ar6' includes N, O, or S as a heteroelement. Preferably it contains N.

In another embodiment, Ar5' and Ar6' are the same as or different from each other, and each independently a phenyl group unsubstituted or substituted with a halogen group, a methyl group, a methoxy group, or a trifluoromethyl group; biphenyl group; naphthyl group; thiophene group; or a pyridine group.

In another embodiment, Ar5' and Ar6' are the same as or different from each other, and each independently a phenyl group unsubstituted or substituted with a methyl group; naphthyl group; or a pyridine group.

According to an exemplary embodiment of the present specification, Ar7 is a substituted or unsubstituted m-valent aryl group having 6 to 60 carbon atoms; Or a substituted or C 3 to C 60 m is a cycloalkyl group.

In another exemplary embodiment, Ar7 is a substituted or unsubstituted C6-C30 m-valent aryl group; Or a substituted or C 3-30 m is a cycloalkyl group.

In another embodiment, Ar7 is a substituted or unsubstituted polycyclic m-valent aryl group having 6 to 30 carbon atoms; Or a substituted or monocyclic m having 3 to 30 carbon atoms is a cycloalkyl group.

According to another exemplary embodiment, Ar7 is a substituted or unsubstituted m-valent naphthyl group; a substituted or unsubstituted m-phenanthrenyl group; Or a substituted or unsubstituted m is a cyclohexyl group.

According to an exemplary embodiment of the present specification, Ar7' is a substituted or unsubstituted arylene group having 6 to 60 carbon atoms; or a substituted or cycloalkylene group having 3 to 60 carbon atoms.

In another embodiment, Ar7' is a substituted or unsubstituted arylene group having 6 to 30 carbon atoms; or a substituted or cycloalkylene group having 3 to 30 carbon atoms.

In another embodiment, Ar7' is a substituted or unsubstituted polycyclic arylene group having 6 to 30 carbon atoms; or a substituted or monocyclic cycloalkylene group having 3 to 30 carbon atoms.

According to another exemplary embodiment, Ar7' is a substituted or unsubstituted naphthylene group; a substituted or unsubstituted phenanthrenylene group; or a substituted or unsubstituted cyclohexylene group.

According to an exemplary embodiment of the present specification, m is 2, and Ar7 is any one selected from the following structures. According to another exemplary embodiment, Ar7' is any one selected from the following structures.

와

은 서로 동일하다.According to an exemplary embodiment of the present specification, the formula 2-1

Wow

are identical to each other

와

은 서로 동일하다.According to an exemplary embodiment of the present specification, the formula 2-1

Wow

are identical to each other

According to an exemplary embodiment of the present specification, the compound represented by Formula 2 is represented by any one of the following compounds.

According to an exemplary embodiment of the present invention, the compound of Formula 1 may be prepared as shown in Scheme 1 below, and the compound of Formula 2 may be prepared as shown in Scheme 2 below. Although the following Schemes 1 and 2 describe the synthesis process of some compounds corresponding to Formulas 1 and 2 of the present application, various compounds corresponding to Formulas 1 and 2 of the present application can be synthesized using synthetic procedures such as Schemes 1 and 2 below. And, the substituents may be combined by methods known in the art, and the type, position, and number of the substituents may be changed according to the techniques known in the art.

[Scheme 1]

[Scheme 2]

In Scheme 1, R means a substituent connected to the core, and may be R1 to R3, B1 or B2 of the present invention, and the definition of the remaining substituents is as described above. In Scheme 2, the definition of the substituent is as described above.

The organic light emitting device of the present specification is a conventional organic material layer, except that the first organic material layer is formed using the compound represented by Chemical Formula 1 and the second organic material layer is formed using the compound represented by Chemical Formula 2 described above. It can be manufactured according to the manufacturing method and material of the light emitting device.

The first organic layer including the compound represented by Formula 1 and the second organic layer including the compound represented by Formula 2 may be formed as an organic layer by a solution coating method as well as a vacuum deposition method. Here, the solution coating method means spin coating, dip coating, inkjet printing, screen printing, spraying, roll coating, etc., but is not limited thereto.

The organic material layer of the organic light emitting device of the present specification may have a structure including only the first organic material layer and the second organic material layer, or may have a structure further including an additional organic material layer. As the additional organic material layer, one of a hole injection layer, a hole transport layer, a layer that transports and injects holes at the same time, an electron blocking layer, a light emitting layer, an electron transport layer, an electron injection layer, a layer that simultaneously transports and injects electrons, and a hole blocking layer It can be more than a layer. However, the structure of the organic light emitting device is not limited thereto and may include a smaller number or a larger number of organic material layers.

In the organic light emitting device according to the exemplary embodiment of the present specification, the first electrode is an anode, the second electrode is a cathode, the first organic material layer is a light emitting layer, and the second organic material layer is the second electrode and the first It is provided between the organic material layers. That is, the second organic material layer is provided between the cathode and the light emitting layer.

In the organic light emitting device according to an exemplary embodiment of the present specification, the first organic material layer is a light emitting layer.

In the organic light emitting device according to an exemplary embodiment of the present specification, the first organic material layer is a light emitting layer, and the compound represented by Chemical Formula 1 is included as a dopant of the light emitting layer.

In the organic light emitting device according to an exemplary embodiment of the present specification, the first organic material layer is a light emitting layer, and the compound represented by Formula 1 is used as a dopant of the light emitting layer, and further includes a fluorescent host or a phosphorescent host. In this case, the dopant in the light emitting layer may be included in an amount of 1 to 50 parts by weight based on 100 parts by weight of the host, preferably 0.1 to 30 parts by weight, more preferably 1 to 10 parts by weight. When within the above range, energy transfer from the host to the dopant occurs efficiently.

In one embodiment of the present specification, the host is an anthracene derivative.

In the exemplary embodiment of the present specification, the organic material layer includes two or more light emitting layers, and one of the two or more light emitting layers includes the compound represented by Formula 1 above.

In one embodiment of the present specification, the maximum emission peaks of the two or more emission layers are different from each other. The light emitting layer including the compound represented by Formula 1 has a blue color, and the light emitting layer not including the compound represented by Formula 1 may include a blue, red, or green light emitting compound known in the art.

In an exemplary embodiment of the present specification, the emission layer including the compound represented by Formula 1 includes a fluorescent dopant, and the emission layer not including the compound represented by Formula 1 includes a phosphorescent dopant.

In an exemplary embodiment of the present specification, the maximum emission peak of the emission layer including the compound represented by Formula 1 is 400 nm to 500 nm. That is, the light emitting layer including the compound represented by Formula 1 emits blue light.

The organic material layer of the organic light emitting device according to an exemplary embodiment of the present specification includes two or more light emitting layers, the maximum emission peak of one light emitting layer (light emitting layer 1) is 400 nm to 500 nm, and the other light emitting layer (light emitting layer 2) ) has a maximum emission peak between 510 nm and 580 nm; Alternatively, it may exhibit a maximum emission peak of 610 nm and 680 nm. In this case, the light emitting layer 1 includes the compound represented by Formula 1 above.

In the organic light emitting device according to the exemplary embodiment of the present specification, the second organic material layer is an electron transport region. Specifically, the second organic material layer includes at least one layer selected from the group consisting of a hole blocking layer, an electron transport layer, an electron injection layer, and an electron injection and transport layer.

In the organic light emitting device according to another exemplary embodiment, the second organic material layer includes one or two layers selected from the group consisting of a hole blocking layer, an electron transport layer, an electron injection layer, and an electron injection and transport layer.

In the organic light emitting device according to another exemplary embodiment, the second organic material layer is a hole blocking layer, an electron transport layer, an electron injection layer, or an electron injection and transport layer.

In the organic light emitting diode according to another exemplary embodiment, the second organic material layer is a hole blocking layer.

In the organic light emitting device according to another exemplary embodiment, the second organic material layer is an electron transport layer.

In an organic light emitting diode according to another exemplary embodiment, the second organic material layer is an electron injection and transport layer.

In the organic light emitting diode according to another exemplary embodiment, the second organic material layer includes a hole blocking layer and an electron injection and transport layer. In this case, the hole blocking layer is provided adjacent to the light emitting layer, and the electron injection and transport layer is provided adjacent to the cathode.

In the exemplary embodiment of the present specification, the second organic material layer is provided in contact with the first organic material layer.

In an exemplary embodiment of the present specification, the second organic material layer further includes one or more n-type dopants selected from alkali metals and alkaline earth metals.

When the organic alkali metal compound or the organic alkaline earth metal compound is used as the n-type dopant, it is possible to secure the stability of the hole from the light emitting layer, thereby improving the lifespan of the organic light emitting device. In addition, by adjusting the ratio of the organic alkali metal compound or the organic alkaline earth metal compound to the electron mobility of the electron transport layer, it is possible to maximize the balance between holes and electrons in the light emitting layer, thereby increasing luminous efficiency.

LiQ is more preferable as the n-type dopant used in the second organic material layer in the present specification.

The second organic material layer may include the compound of Formula 2 and the n-type dopant in a weight ratio of 1:9 to 9:1. Preferably, the compound of Formula 2 and the n-type dopant may be included in an amount of 2:8 to 8:2, more preferably 3:7 to 7:3.

In the exemplary embodiment of the present specification, the first electrode is an anode, and the second electrode is a cathode.

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

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

The structure of the organic light emitting device of the present specification may have a structure as shown in FIGS. 1, 2 and 8 , but is not limited thereto.

1 shows a substrate 1, an anode 2, a hole injection layer 3, a hole transport layer 4, a light emitting layer 6, a hole blocking layer 7, an electron injection and transport layer 8, and a cathode 11 The structure of this sequentially stacked organic light emitting device is exemplified. In such a structure, the compound represented by Formula 1 may be included in the light emitting layer 6 , and the compound represented by Formula 2 may be included in the hole blocking layer 7 or the electron injection and transport layer 8 .

2 shows a substrate 1, an anode 2, a hole injection layer 3, a hole transport layer 4, an electron blocking layer 5, a light emitting layer 6, an electron injection and transport layer 8, and a cathode 11 The structure of this sequentially stacked organic light emitting device is exemplified. In such a structure, the compound represented by Formula 1 may be included in the emission layer 6 , and the compound represented by Formula 2 may be included in the electron injection and transport layer 8 .

8 shows a substrate 1, an anode 2, a p-doped hole transport layer 4p, a hole transport layer 4R, 4G, 4B, a light emitting layer 6RP, 6GP, 6BF, a first electron transport layer 9a, The structure of the organic light emitting device in which the second electron transport layer 9b, the electron injection layer 10, the cathode 11 and the capping layer 14 are sequentially stacked is illustrated. In such a structure, the compound represented by Chemical Formula 1 may be included in the light emitting layers 6RP, 6GP, and 6BF, and the compound represented by Chemical Formula 2 may include a first electron transport layer 9a and a second electron transport layer 9b. And it may be included in one or more layers of the electron injection layer (10).

According to an exemplary embodiment of the present specification, the organic light emitting device may have a tandem structure in which two or more independent devices are connected in series. In an exemplary embodiment, the tandem structure may have a form in which each organic light emitting device is bonded to a charge generating layer. Since a device having a tandem structure can be driven at a lower current than a unit device based on the same brightness, there is an advantage in that the lifespan characteristics of the device are greatly improved.

According to an exemplary embodiment of the present specification, the organic material layer may include: a first stack including one or more light emitting layers; a second stack comprising at least one light emitting layer; and one or more charge generation layers provided between the first stack and the second stack.

According to an exemplary embodiment of the present specification, the organic material layer includes: a first stack including one or more light emitting layers; a second stack comprising one or more light emitting layers; and a third stack including one or more light emitting layers, between the first stack and the second stack; and one or more charge generation layers, respectively, between the second stack and the third stack.

In the present specification, the charge generating layer (Charge Generating layer) means a layer in which holes and electrons are generated when a voltage is applied. The charge generation layer may be an N-type charge generation layer or a P-type charge generation layer. As used herein, the N-type charge generation layer refers to a charge generation layer located closer to the anode than the P-type charge generation layer, and the P-type charge generation layer refers to a charge generation layer located closer to the cathode than the N-type charge generation layer.

The N-type charge generation layer and the P-type charge generation layer may be provided in contact with each other, and in this case, an NP junction is formed. By the NP junction, holes are easily formed in the P-type charge generation layer and electrons are easily formed in the N-type charge generation layer. Electrons are transported in the anode direction through the LUMO level of the N-type charge generating layer, and holes are transported in the cathode direction through the HOMO level of the P-type organic material layer.

The first stack, the second stack, and the third stack each include one or more light emitting layers, and further include a hole injection layer, a hole transport layer, an electron blocking layer, an electron injection layer, an electron transport layer, a hole blocking layer, a hole transport and a hole It may further include one or more layers of a layer for simultaneous injection (a hole injection and transport layer), and a layer for simultaneously performing an electron transport and electron injection (electron injection and transport layer).

An organic light emitting diode including the first stack and the second stack is illustrated in FIG. 3 .

3 shows a substrate 1, an anode 2, a hole injection layer 3, a first hole transport layer 4a, an electron blocking layer 5, a first light emitting layer 6a, a first electron transport layer 9a, An N-type charge generation layer 12, a P-type charge generation layer 13, a second hole transport layer 4b, a second light emitting layer 6b, an electron injection and transport layer 8, and a cathode 11 are sequentially stacked The structure of the organic light emitting device is illustrated. In such a structure, the compound represented by Chemical Formula 1 may be included in the first emission layer 6a or the second emission layer 6b, and the compound represented by Chemical Formula 2 is the first electron transport layer 9a or electron injection. and the transport layer 8 .

The organic light emitting diodes including the first to third stacks are illustrated in FIGS. 4 to 7 .

4 shows a substrate 1, an anode 2, a hole injection layer 3, a first hole transport layer 4a, an electron blocking layer 5, a first light emitting layer 6a, a first electron transport layer 9a, The first N-type charge generation layer 12a, the first P-type charge generation layer 13a, the second hole transport layer 4b, the second light-emitting layer 6b, the second electron transport layer 9b, the second N-type charge An organic layer in which the generation layer 12b, the second P-type charge generation layer 13b, the third hole transport layer 4c, the third light emitting layer 6c, the third electron transport layer 9c and the cathode 11 are sequentially stacked The structure of the light emitting device is illustrated. In such a structure, the compound represented by Formula 1 may be included in the first light-emitting layer 6a, the second light-emitting layer 6b, and the third light-emitting layer 6c, and the compound represented by Formula 2 is the first electron It may be included in one or more layers of the transport layer 9a, the second electron transport layer 9b, and the third electron transport layer 9c.

5 shows a substrate 1, an anode 2, a hole injection layer 3, a first hole transport layer 4a, a second hole transport layer 4b, a first blue fluorescent light emitting layer 6BFa, a first electron transport layer ( 9a), first N-type charge generation layer 12a, first P-type charge generation layer 13a, third hole transport layer 4c, red phosphorescence emission layer 6RP, yellow green phosphorescence emission layer 6YGP, green phosphorescence Light emitting layer 6GP, second electron transport layer 9b, second N-type charge generation layer 12b, second P-type charge generation layer 13b, fourth hole transport layer 4d, fifth hole transport layer 4e , the second blue fluorescent light emitting layer 6BFb, the third electron transport layer 9c, the electron injection layer 10, the cathode 11, and the capping layer 14 are sequentially stacked, the structure of the organic light emitting device is exemplified. In such a structure, the compound represented by Chemical Formula 1 may be included in the first blue fluorescent light emitting layer 6BFa or the second blue fluorescent light emitting layer 6BFb, and the compound represented by Chemical Formula 2 is the first electron transport layer 9a. ), the second electron transport layer 9b, the third electron transport layer 9c, and the electron injection layer 10 may be included in one or more layers.

6 shows a substrate 1, an anode 2, a hole injection layer 3, a first hole transport layer 4a, a second hole transport layer 4b, a first blue fluorescent light emitting layer 6BFa, a first electron transport layer ( 9a), the first N-type charge generation layer 12a, the first P-type charge generation layer 13a, the third hole transport layer 4c, the red phosphorescent emission layer 6RP, the green phosphorescence emission layer 6GP, the second electrons Transport layer 9b, second N-type charge generation layer 12b, second P-type charge generation layer 13b, fourth hole transport layer 4d, fifth hole transport layer 4e, second blue fluorescent light emitting layer 6BFb ), the third electron transport layer 9c, the electron injection layer 10, the cathode 11, and the capping layer 14 are sequentially stacked, the structure of the organic light emitting device is exemplified. In such a structure, the compound represented by Chemical Formula 1 may be included in the first blue fluorescent light emitting layer 6BFa or the second blue fluorescent light emitting layer 6BFb, and the compound represented by Chemical Formula 2 is the first electron transport layer 9a. ), the second electron transport layer 9b, the third electron transport layer 9c, and the electron injection layer 10 may be included in one or more layers.

7 shows a substrate 1, an anode 2, a first p-doped hole transport layer 4pa, a first hole transport layer 4a, a second hole transport layer 4b, a first blue fluorescent light emitting layer 6BFa, The first electron transport layer 9a, the first N-type charge generation layer 12a, the first P-type charge generation layer 13a, the third hole transport layer 4c, the fourth hole transport layer 4d, the second blue fluorescence Light emitting layer 6BFb, second electron transport layer 9b, second N-type charge generation layer 12b, second P-type charge generation layer 13b, fifth hole transport layer 4e, sixth hole transport layer 4f , the third blue fluorescent light emitting layer 6BFc, the third electron transport layer 9c, the electron injection layer 10, the cathode 11, and the capping layer 14 are sequentially stacked, the structure of the organic light emitting device is exemplified. In such a structure, the compound represented by Formula 1 may be included in one or more layers of the first blue fluorescent light-emitting layer 6BFa, the second blue fluorescent light-emitting layer 6BFb, and the third blue fluorescent light-emitting layer 6BFb, The compound represented by Formula 2 may be included in one or more layers of the first electron transport layer 9a, the second electron transport layer 9c, the third electron transport layer 9c, and the electron injection layer 10 .

The N-type charge generation layer is 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4TCNQ), fluorine-substituted 3,4,9,10-pe Lylenetetracarboxylic dianhydride (PTCDA), cyano-substituted PTCDA, naphthalenetetracarboxylic dianhydride (NTCDA), fluorine-substituted NTCDA, cyano-substituted NTCDA, hexaazatriphenylline derivatives and the like, but is not limited thereto. In an exemplary embodiment, the N-type charge generation layer may include a benzimidazophenanthrine-based derivative and a metal of Li at the same time.

The P-type charge generation layer may include an arylamine-based derivative and a compound including a cyano group at the same time.

The organic light emitting device of the present specification may be manufactured using materials and methods known in the art, except that the organic material layer includes the compound.

When the organic light emitting device includes a plurality of organic material layers, the organic material layers may be formed of the same material or different materials. The organic light emitting device according to the present specification forms an anode by depositing a metal or a conductive metal oxide or an alloy thereof on a substrate, and after forming an organic material layer including the above-described first organic material layer and the second organic material layer thereon, It can be prepared by depositing a material that can be used as a cathode thereon. In addition to this method, an organic light emitting device may be manufactured by sequentially depositing a cathode material, an organic material layer, and an anode material on a substrate.

The organic material layer including the first organic material layer and the second organic material layer further includes a hole injection layer, a hole transport layer, an electron injection and transport layer, an electron blocking layer, a light emitting layer, an electron transport layer, an electron injection layer, an electron injection and transport layer, a hole blocking layer, etc. It may be a multi-layered structure. 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 as the anode material, a material having a large work function is preferable 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 negative electrode 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 to the light emitting layer, and has a single layer or a multilayer structure of two or more layers. The hole injection material is a material capable of well injecting holes from the anode at a low voltage, and it is preferable that the highest occupied molecular orbital (HOMO) of the hole injection material is between the work function of the positive electrode material and the HOMO of the surrounding organic material 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. In one embodiment of the present specification, the hole injection layer has a two-layer structure, and each layer includes the same or different materials from each other.

The hole transport layer may serve to facilitate hole transport, and has a single-layer or multi-layered structure of two or more layers. 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. 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. In one embodiment of the present specification, the hole transport layer has a two-layer structure, and each layer includes the same or different materials from each other.

The hole injection and transport layer is a layer that simultaneously transports and injects holes, and a hole transport layer material and/or a hole injection layer material known in the art may be used.

The electron injection and transport layer is a layer that simultaneously transports and injects electrons, and an electron transport layer material and/or an electron injection layer material known in the art may be used.

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

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 (Alq3); 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 Alq ₃ (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-F ₂ ppy) ₂ Irpic, spiro-DPVBi, spiro-6P, distylbenzene (DSB), and distrylarylene (DSA). ), a PFO-based polymer, a fluorescent material such as 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 serves to facilitate the transport of electrons. As the electron transport material, a material capable of receiving electrons from the cathode and transferring them to the light emitting layer is suitable, and a material having high electron mobility is suitable. Specific examples include Al complex of 8-hydroxyquinoline; complexes containing Alq ₃ ; organic radical compounds; hydroxyflavone-metal complexes, and the like, but are not limited thereto.

The electron injection layer serves to facilitate electron injection. As the electron injection material, a compound having an ability to transport electrons, an electron injection effect from the cathode, an excellent electron injection effect for a light emitting layer or a light emitting material, and an excellent thin film formation 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 organic light emitting device according to the present specification may be a top emission type, a back emission type, or a double side emission type depending on the material used.

Hereinafter, in order to describe the present specification in detail, it will be described in detail with reference to Examples and Comparative Examples. However, the Examples and Comparative Examples according to the present specification may be modified in various other forms, and the scope of the present specification is not to be construed as being limited to the Examples and Comparative Examples described below. Examples and comparative examples of the present specification are provided to more completely explain the present specification to those of ordinary skill in the art.

Synthesis Example 1. Synthesis of compound 1

1) Synthesis of Intermediate 1

Under nitrogen atmosphere, 1-bromo-2,3-dichloro-5-methylbenzene [1-bromo-2,3-dichloro-5-methylbenzene] 100 g, amine A-1 117 g, sodium tertbutoxide (sodium tert) -butoxide) 60 g, bis(tri-tertbutylphosphine)palladium(0) (Pd(P(t-Bu) ₃ ) ₂ ) 2.1 g were put in 3.0 L of toluene, and then heated at 120 ^o C for 2 hours. stirred for a while. After completion of the reaction, the reaction solution was cooled to room temperature, water and NH ₄ Cl were added to separate the mixture, and the mixture was treated with MgSO ₄ (anhydrous) and filtered. The filtered solution was distilled off under reduced pressure and purified by recrystallization (toluene/hexane) to obtain 130 g of Intermediate 1. (Yield 82%, Mass [M+]=441)

2) Synthesis of Intermediate 2

Under nitrogen atmosphere, 30 g of Intermediate 1, 28 g of Compound A-2, 9.8 g of sodium tert-butoxide, bis(tri-tertbutylphosphine)palladium(0) (Pd(P(t-Bu) ₃ ) ) ₂ ) After putting 0.7 g of toluene in 550 mL of toluene, it was heated at 150 ^o C and stirred for 8 hours. After completion of the reaction, the reaction solution was cooled to room temperature, water and NH ₄ Cl were added to separate the mixture, and the mixture was treated with MgSO ₄ (anhydrous) and filtered. The filtered solution was distilled off under reduced pressure and purified by recrystallization (toluene/hexane) to obtain 42 g of Intermediate 2. (Yield 76%, Mass [M+]=810)

3) Synthesis of compound 1

In a flask containing 42 g of Intermediate 2 dissolved in 400 mL of toluene (anhydrous) cooled to 0 ^o C under a nitrogen atmosphere, 122 mL of tert-butyllithium (t-BuLi (1.7M in pentane)) was slowly added dropwise to 60 It was stirred at ^o C for 3 hours. When the lithium halogen exchange reaction was completed, it was cooled to 0 ^o C again, and 7.5 mL of boron tribromide (BBr ₃ ) was slowly added dropwise, and then the temperature was raised to 70 ^o C and stirred for 10 hours. After completion of the reaction, the reaction solution was cooled to room temperature, water and NH ₄ Cl were added to separate the mixture, and the mixture was treated with MgSO ₄ (anhydrous) and filtered. The filtered solution was distilled off under reduced pressure and purified by recrystallization (toluene/hexane) to obtain 9.5 g of Compound 1. (Yield 23%, Mass [M+]=783)

Synthesis Example 2. Synthesis of compound 2

1) Synthesis of Intermediate 3

20 g of 2-bromo-1,3-diiodo-5-methylbenzene [2-bromo-1,3-diiodo-5-methylbenzene] under nitrogen atmosphere, 38 g of amine A-2, sodium tertbutoxide (sodium 14 g of tert-butoxide) and 0.24 g of bis(tri-tertbutylphosphine)palladium(0) (Pd(P(t-Bu) ₃ ) ₂ ) were added to 450 mL of toluene, and then heated at 120 ^o C 4 stirred for hours. After completion of the reaction, the reaction solution was cooled to room temperature, water and NH ₄ Cl were added to separate the mixture, and the mixture was treated with MgSO ₄ (anhydrous) and filtered. The filtered solution was distilled off under reduced pressure and purified by recrystallization (toluene/hexane) to obtain 35 g of Intermediate 3. (Yield 76%, Mass [M+]=979)

2) Synthesis of compound 2

In a flask containing 35 g of Intermediate 3 dissolved in 300 mL of toluene (anhydrous) cooled to 0 ^o C under a nitrogen atmosphere, 35 mL of n-butyllithium (n-BuLi(2.5M in hexane)) was slowly added dropwise to 60 It was stirred at ^o C for 1 hour. When the lithium halogen exchange reaction was completed, it was cooled to 0 ^o C again, and 5.2 mL of boron tribromide (BBr ₃ ) was slowly added dropwise, and then the temperature was raised to 70 ^o C and stirred for 6 hours. After completion of the reaction, the reaction solution was cooled to room temperature, water and NH ₄ Cl were added to separate the mixture, and the mixture was treated with MgSO ₄ (anhydrous) and filtered. The filtered solution was distilled off under reduced pressure and purified by recrystallization (toluene/hexane) to obtain 9.0 g of Compound 2. (Yield 34%, Mass [M+]=908)

Synthesis Example 3. Synthesis of compound 3

1) Synthesis of intermediates 4 and 5

18 g of Intermediate 4 was obtained in the same manner as in Preparation of Intermediate 1 of Synthesis Example 1. except that 18 g of amine A-3 was used instead of amine A-1. (Yield 75%, Mass [M+]=579)

In addition, 18 g of Intermediate 5 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. Except that 18 g of Intermediate 4 was used instead of Intermediate 1 and 8.8 g of amine A-1 was used instead of amine A-2. (Yield 70%, Mass [M+]=824)

2) Synthesis of compound 3

It was prepared in the same manner as in Synthesis Example 1. Compound 1 of Synthesis Example 1. Except that 18 g of Intermediate 5 was used instead of Intermediate 2, 4.0 g of Compound 3 was obtained. (Yield 23%, Mass [M+]=797)

Synthesis Example 4. Synthesis of compound 4

14.5 g of Intermediate 6 was obtained in the same manner as in Preparation of Intermediate 2 of Synthesis Example 1. except that 9.5 g of amine A-4 was used instead of amine A-2. (Yield 78%, Mass [M+]=824)

It was prepared in the same manner as in Synthesis Example 1. Compound 1 of Synthesis Example 1. Except that 14.5 g of Intermediate 6 was used instead of Intermediate 2, 3.1 g of Compound 4 was obtained. (Yield 22%, Mass [M+]=797)

Synthesis Example 5. Synthesis of compound 5

1) Synthesis of Intermediate 7

3-bromo-4,5-dichlorophenol [3-bromo-4,5] instead of 1-bromo-2,3-dichloro-5-methylbenzene [1-bromo-2,3-dichloro-5-methylbenzene] -dichlorophenol] The amination reaction was carried out in the same manner as in the preparation of Intermediate 1 of Synthesis Example 1. except that 20 g was used, and then the following reaction was carried out without purification.

After dissolving the amination reaction product in 420 mL of dimethylformamide (DMF), 34 g of potassium carbonate was added at room temperature, and then 22 mL of perfluorobutanesulfonyl fluoride at 0 °C. was added dropwise. After the reaction was completed by stirring for 2 hours, 400 mL of water and 200 mL of ethyl acetate were added and stirred for 30 minutes. The organic layer was washed with aq. Wash twice with NaCl. The separated organic layer was collected, treated with Mg ₂ SO ₄ (anhydrous) and filtered. The solvent of the filtered solution was distilled off under reduced pressure and purified by recrystallization (ethyl acetate/hexane) to obtain 40 g of Intermediate 7. (Yield 77%, Mass [M+]=725)

2) Synthesis of Intermediate 8

Intermediate 7 20g, amine A-5 4.7g, tris(dibenzylideneacetone)dipalladium(0)[Palladium(0)bis(dibenzylideneacetone)](Pd(dba) ₂ )0.16g, 2-Dicyclohexylphosphino-2', A flask containing 0.26 g of 4',6'-triisopropylbiphenyl (Xphos), 18 g of cesium carbonate, and 300 mL of xylene was heated at 130° C. and stirred for 12 hours. The reaction solution was cooled to room temperature, and sat. aq. After separation by adding NH ₄ Cl and toluene, the solvent was distilled off under reduced pressure. 13 g of intermediate 8 was obtained by purification by column chromatography (ethylacetate/hexane). (Yield 77%, Mass [M+]=594)

3) Synthesis of Intermediate 9

17 g of Intermediate 9 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 13 g of Intermediate 8 was used instead of Intermediate 1. (Yield 81%, Mass [M+]=963)

4) Synthesis of compound 5

3.5 g of compound 5 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 17 g of Intermediate 9 was used instead of Intermediate 2. (Yield 21%, Mass [M+]=937)

Synthesis Example 6. Synthesis of compound 6

15 g of Intermediate 10 was obtained in the same manner as in Preparation of Intermediate 2 of Synthesis Example 1. except that 11 g of amine A-6 was used instead of amine A-2. (Yield 75%, Mass [M+]=886)

3.0 g of compound 6 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 15 g of Intermediate 10 was used instead of Intermediate 2. (Yield 21%, Mass [M+]=860)

Synthesis Example 7. Synthesis of compound 7

13 g of Intermediate 11 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 9.7 g of A-7 was used instead of amine A-2. (Yield 69%, Mass [M+]=830)

3.0 g of Compound 7 was obtained in the same manner as in the preparation of Compound 1 of Synthesis Example 1. except that 5.0 g of Intermediate 11 was used instead of Intermediate 2. (Yield 24%, Mass [M+]=804)

Synthesis Example 8. Synthesis of compound 8

20 g of Intermediate 12 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 14 g of A-8 was used instead of amine A-2. (Yield 72%, Mass [M+]=820)

4.2 g of compound 8 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 20 g of Intermediate 12 was used instead of Intermediate 2. (Yield 22%, Mass [M+]=792)

Synthesis Example 9. Synthesis of compound 9

16 g of Intermediate 13 was obtained in the same manner as in Synthesis Example 5. Preparation of Intermediate 8 except that 14 g of A-9 was used instead of amine A-5. (Yield 68%, Mass [M+]=853)

18 g of Intermediate 14 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 16 g of Intermediate 13 was used instead of Intermediate 1. (Yield 78%, Mass [M+]=1222)

3.6 g of compound 9 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 18 g of Intermediate 14 was used instead of Intermediate 2. (Yield 20%, Mass [M+]=1195)

Synthesis Example 10. Synthesis of compound 10

43 g of Intermediate 15 was obtained in the same manner as in Preparation of Intermediate 2 of Synthesis Example 1. except that 28 g of A-10 was used instead of amine A-2. (Yield 77%, Mass [M+]=824)

8.9 g of compound 10 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 43 g of Intermediate 15 was used instead of Intermediate 2. (Yield 21%, Mass [M+]=797)

Synthesis Example 11. Synthesis of compound 11

41 g of Intermediate 16 was obtained in the same manner as in Preparation of Intermediate 2 of Synthesis Example 1. except that 29 g of A-11 was used instead of amine A-2. (Yield 72%, Mass [M+]=834)

6.7 g of compound 11 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 41 g of Intermediate 16 was used instead of Intermediate 2. (Yield 17%, Mass [M+]=807)

Synthesis Example 12. Synthesis of compound 12

18 g of Intermediate 17 was obtained in the same manner as in the preparation of Intermediate 1 of Synthesis Example 1. except that 17 g of A-2 was used instead of amine A-1. (Yield 76%, Mass [M+]=565)

24 g of Intermediate 18 was obtained in the same manner as in Synthesis Example 1. Intermediate 2, except that 18 g of Intermediate 17 instead of Intermediate 1 and 17 g of A-12 instead of amine A-2 were used. (Yield 72%, Mass [M+]=1046)

5.1 g of Compound 12 was obtained in the same manner as in the preparation of Compound 1 of Synthesis Example 1. except that 24 g of Intermediate 18 was used instead of Intermediate 2. (Yield 22%, Mass [M+]=1020)

Synthesis Example 13. Synthesis of compound 13

Intermediate 1 of Synthesis Example 1. except that 5.0 g of 1-bromo-2,3-dichloro-5-(methyl-d3)-benzene was used instead of 1-bromo-2,3-dichloro-5-methylbenzene 13 g of Intermediate 19 was obtained in the same manner as in the preparation method. (Yield 71%, Mass [M+]=444)

14 g of Intermediate 20 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. Except that 13 g of Intermediate 19 instead of Intermediate 1 and 8.8 g of A-13 instead of amine A-2 were used. (Yield 67%, Mass [M+]=709)

3.4 g of compound 13 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 14 g of Intermediate 20 was used instead of Intermediate 2. (Yield 25%, Mass [M+]=682)

Synthesis Example 14. Synthesis of compound 14

13 g of Intermediate 21 was obtained in the same manner as in the preparation of Intermediate 8 of Synthesis Example 5. except that 6.2 g of A-14 was used instead of amine A-5. (Yield 72%, Mass [M+]=650)

18 g of Intermediate 22 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. Except that 16 g of Intermediate 21 was used instead of Intermediate 1, and 11 g of A-15 was used instead of amine A-2. (Yield 77%, Mass [M+]=1172)

It was prepared in the same manner as in Synthesis Example 1. Compound 1 of Synthesis Example 1. Except that 18 g of Intermediate 22 was used instead of Intermediate 2, 4.0 g of Compound 14 was obtained. (Yield 23%, Mass [M+]=1145)

Synthesis Example 15. Synthesis of compound 15

14 g of Intermediate 23 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 9.9 g of A-16 was used instead of amine A-2. (Yield 73%, Mass [M+]=840)

2.7 g of Compound 15 was obtained in the same manner as in the preparation of Compound 1 of Synthesis Example 1. except that 14 g of Intermediate 23 was used instead of Intermediate 2. (Yield 20%, Mass [M+]=814)

Synthesis Example 16. Synthesis of compound 16

15 g of Intermediate 24 was obtained in the same manner as in Preparation of Intermediate 2 of Synthesis Example 1. except that 13.3 g of A-17 was used instead of amine A-2. (Yield 67%, Mass [M+]=989)

3.0 g of compound 16 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 15 g of Intermediate 24 was used instead of Intermediate 2. (Yield 21%, Mass [M+]=963)

Synthesis Example 17. Synthesis of compound 17

20 g of Intermediate 25 was obtained in the same manner as in Preparation of Intermediate 2 of Synthesis Example 1. except that 17.1 g of A-18 was used instead of amine A-2. (Yield 65%, Mass [M+]=908)

4.1 g of compound 17 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 20 g of Intermediate 25 was used instead of Intermediate 2. (Yield 21%, Mass [M+]=882)

Synthesis Example 18. Synthesis of compound 18

14 g of Intermediate 26 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 12. g of A-19 was used instead of amine A-2. (Yield 66%, Mass [M+]=938)

2.9 g of compound 18 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 14 g of Intermediate 26 was used instead of Intermediate 2. (Yield 21%, Mass [M+]=912)

Synthesis Example 19. Synthesis of compound 19

19 g of Intermediate 27 was obtained in the same manner as in the preparation of Intermediate 20 of Synthesis Example 13. except that 17 g of A-20 was used instead of amine A-13. (Yield 62%, Mass [M+]=911)

3.6 g of compound 19 was obtained in the same manner as in the preparation of compound 13 of Synthesis Example 13. except that 19 g of Intermediate 27 was used instead of Intermediate 20. (Yield 20%, Mass [M+]=885)

Synthesis Example 20. Synthesis of compound 20

Same as the preparation method of Intermediate 1 of Synthesis Example 1. except that 10 g of 1-bromo-2,3-dichloro-5-tertbutylbenzene was used instead of 1-bromo-2,3-dichloro-5-methylbenzene 13 g of intermediate 28 was obtained. (Yield 76%, Mass [M+]=483)

18 g of Intermediate 29 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. Except that 13 g of Intermediate 28 instead of Intermediate 1 and 14 g of A-18 instead of amine A-2 were used. (Yield 70%, Mass [M+]=950)

3.4 g of Compound 20 was obtained in the same manner as in the preparation of Compound 1 of Synthesis Example 1. except that 18 g of Intermediate 29 was used instead of Intermediate 2. (Yield 19%, Mass [M+]=924)

Synthesis Example 21. Synthesis of compound 21

12 g of Intermediate 30 was obtained in the same manner as in the preparation of Intermediate 1 of Synthesis Example 1. except that 11 g of A-21 was used instead of A-1. (Yield 70%, Mass [M+]=413)

17 g of Intermediate 31 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 12 g of Intermediate 30 was used instead of Intermediate 1 and 13.5 g of A-22 was used instead of amine A-2. (Yield 70%, Mass [M+]=839)

3.2 g of Compound 21 was obtained in the same manner as in the preparation of Compound 1 of Synthesis Example 1. except that 17 g of Intermediate 31 was used instead of Intermediate 2. (Yield 19%, Mass [M+]=813)

Synthesis Example 22. Synthesis of compound 22

Synthesis Example 1 except that 10 g of 1-bromo-3-chloro-5-methylbenzene was used instead of 1-bromo-2,3-dichloro-5-methylbenzene and 22 g of amine A-23 was used instead of amine A-1 21 g of Intermediate 32 was obtained in the same manner as in the preparation of Intermediate 1 of . (Yield 74%, Mass [M+]=581)

Under nitrogen atmosphere, 21 g of Intermediate 32, 4.4 g of 2,4-dimethylaniline, 5.2 g of sodium tert-butoxide, bis(tri-tertbutylphosphine)palladium(0) (Pd(P(t-) Bu) ₃ ) ₂ ) 0.36 g was added to 300 mL of toluene, and then heated at 120 ^o C and stirred for 4 hours. Immediately after completion of the amination reaction, 6.9 g of 1-bromo-3-chlorobenzene was added dropwise, followed by stirring for 2 hours. After completion of the reaction, the reaction solution was cooled to room temperature, water and NH ₄ Cl were added to separate the mixture, and then treated with MgSO ₄ (anhydrous) and filtered. The filtered solution was distilled off under reduced pressure and purified by recrystallization (toluene/hexane) to obtain 17 g of Intermediate 33. (Yield 61%, Mass [M+]=776)

17 g of intermediate 33 was dissolved in dichlorobenzene under a nitrogen atmosphere, and 14 g of boron triiodide (BI ₃ ) was added dropwise, followed by heating to 130 ^o C and stirring for 4 hours. After completion of the reaction, the reaction solution was cooled to room temperature, dissolved in toluene, extracted, treated with MgSO ₄ (anhydrous), and filtered. The filtered solution was distilled off under reduced pressure and purified by recrystallization (toluene/hexane) to obtain 5.5 g of intermediate 34. (Yield 32%, Mass [M+]=784)

17 g of Compound 22 was obtained in the same manner as in Synthesis Example 1. Intermediate 2, except that 5.5 g of Intermediate 34 instead of Intermediate 1 and 1.2 g of A-5 instead of amine A-2 were used. (Yield 81%, Mass [M+]=917)

Synthesis Example 23. Synthesis of compound 23

20 g of Intermediate 35 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 15 g of Intermediate 8 instead of Intermediate 1 and 13 g of A-18 instead of amine A-2 were used. (Yield 75%, Mass [M+]=1061)

3.5 g of compound 23 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 20 g of Intermediate 35 was used instead of Intermediate 2. (Yield 18%, Mass [M+]=1035)

Synthesis Example 24. Synthesis of compound 24

Dissolve 50.0 g of 1.3-dibromo-2-chloro-5-iodobenzene (1,3-dibromo-2-chloro-5-iodobenzene) in 1.2 L of tetrahydrofuran (THF) under a nitrogen atmosphere, and then adjust the temperature to - It was maintained at 10 °C. Next, isopropylmagnesium chloride (isopropylmagnesium chloride) 70 mL (2.0 M in THF) was slowly added dropwise, followed by stirring at 0° C. for 1 hour. At the same temperature, 37.2 g of chlorotriphenylsilane was added. The reaction solution was heated to 0° C. and stirred for about 1 hour, followed by stirring at room temperature for an additional 12 hours. Then, after dilution with ethyl acetate, Saturated aq. NH ₄ Cl was added to terminate the reaction, and the organic layer was extracted, treated with MgSO ₄ (anhydrous) and filtered. The filtered solution was distilled off under reduced pressure and purified by recrystallization (toluene/hexane) to obtain 36 g of Intermediate 36. (Yield 54%, Mass [M+]=529)

Prepared in the same manner as in the preparation of Intermediate 3 of Synthesis Example 2. Except for using 20 g of Intermediate 36 instead of 2-bromo-1,3-diiodo-5-methylbenzene and 21 g of amine A-1 instead of amine A-2 Thus, 25 g of intermediate 37 was obtained. (Yield 71%, Mass [M+]=930)

4.6 g of Compound 24 was obtained in the same manner as in the preparation of Compound 1 of Synthesis Example 1. except that 25 g of Intermediate 37 was used instead of Intermediate 2. (Yield 19%, Mass [M+]=904)

* Synthesis Example 25. Synthesis of compound 25

An intermediate prepared in the same manner as in the preparation method of Intermediate 3 of Synthesis Example 2. except that 15 g of 1,3-dibromo-2-chlorobenzene was used instead of 2-bromo-1,3-diiodo-5-methylbenzene 28 g of 38 were obtained. (Yield 75%, Mass [M+]=672)

6.8 g of Intermediate 39 was obtained in the same manner as in the preparation of Compound 1 of Synthesis Example 1. except that 28 g of Intermediate 38 was used instead of Intermediate 2. (Yield 25%, Mass [M+]=645)

6.8 g of Intermediate 39 was dissolved in 100 mL of chloroform under a nitrogen atmosphere, and 1.9 g of N -bromosuccinimide was added over 30 minutes, followed by stirring at room temperature for 4 hours. Distilled water was added to the reaction solution to terminate the reaction, and the organic layer was extracted, treated with MgSO ₄ (anhydrous), and filtered. The filtered solution was distilled off under reduced pressure and purified by column chromatography (eluent: hexane/ethyl acetate = 1:1 (volume ratio)) to obtain 5.2 g of Intermediate 40. (Yield 68%, Mass [M+]=724)

In a nitrogen atmosphere, 5.2 g of Intermediate 40 was dissolved in 60 mL of tetrahydrofuran (THF anhydrous) under nitrogen conditions, and then the temperature was lowered to -78 °C. Next, 5.7 mL of n-butyllithium (n-BuLi (2.5M in hexane)) was slowly added dropwise, followed by stirring for 1 hour. When the lithium halogen exchange reaction was completed, 1.2 mL of chlorotrimethylsilane was dissolved in 5 mL of tetrahydrofuran (anhydrous), and then slowly added dropwise. After the reaction solution was stirred for about 1 hour while maintaining the temperature at -78°C, the organic layer was extracted using methylene chloride, treated with MgSO ₄ (anhydrous), and filtered. The filtered solution was distilled off under reduced pressure and purified by column chromatography (eluent: hexane/ethyl acetate = 1:1 (volume ratio)) to obtain 3.5 g of compound 25. (Yield 68%, Mass [M+]=747).

Synthesis Example 26. Synthesis of compound 26

22 g of Intermediate 41 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 16 g of A-24 was used instead of amine A-2. (Yield 75%, Mass [M+]=860)

4.2 g of compound 26 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 14 g of Intermediate 41 was used instead of Intermediate 2. (Yield 20%, Mass [M+]=833)

Synthesis Example 27. Synthesis of compound 27

20 g of Intermediate 42 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 12.6 g of A-25 was used instead of amine A-2. (Yield 76%, Mass [M+]=773)

4.1 g of compound 27 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 20 g of Intermediate 42 was used instead of Intermediate 2. (Yield 21%, Mass [M+]=746)

Synthesis Example 28. Synthesis of compound 28

17 g of Intermediate 43 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. Except that 15 g of Intermediate 21 was used instead of Intermediate 1 and A-26 was used instead of amine A-2. (Yield 67%, Mass [M+]=1106)

3.6 g of compound 28 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 17 g of Intermediate 43 was used instead of Intermediate 2. (Yield 22%, Mass [M+]=1079)

Synthesis Example 29. Synthesis of compound 29

16 g of Intermediate 44 was obtained in the same manner as in the preparation of Intermediate 1 of Synthesis Example 1. except that 12.8 g of A-27 was used instead of A-1. (Yield 70%, Mass [M+]=365)

26 g of Intermediate 45 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 16 g of Intermediate 44 instead of Intermediate 1 and 22 g of A-18 instead of amine A-2 were used. (Yield 71%, Mass [M+]=832)

4.1 g of compound 29 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 17 g of Intermediate 45 was used instead of Intermediate 2. (Yield 16%, Mass [M+]=805)

Synthesis Example 30. Synthesis of compound 30

22 g of Intermediate 46 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 17.8 g of A-28 was used instead of amine A-2. (Yield 70%, Mass [M+]=926)

4.3 g of compound 30 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 22 g of Intermediate 46 was used instead of Intermediate 2. (Yield 20%, Mass [M+]=900)

Synthesis Example 31. Synthesis of compound 31

Intermediate 7 20 g, 2-fluoroboronic acid 4.6 g, potassium phosphate 11.7 g 1,4-dioxane 220 mL and 50 mL water were added, and then tetrakis (triphenylphosphine) palladium (0) [ After adding 0.48 g of tetrakis(triphenylhosphine)palladium(0)]Pd(PPh ₃ ) ₄ , the mixture was heated and stirred for 16 hours. After completion of the reaction, the reaction solution was cooled to room temperature, the organic solvent was removed, dissolved in toluene for extraction, and the organic solvent was treated with MgSO ₄ (anhydrous) and filtered. The filtered solution was distilled off under reduced pressure and purified by recrystallization (toluene/hexane) to obtain 9.5 g of intermediate 47. (Yield 66%, Mass [M+]=521)

14 g of Intermediate 48 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 9.1 g of A-29 was used instead of amine A-2. (Yield 78%, Mass [M+]=982)

3.2 g of Compound 31 was obtained in the same manner as in the preparation of Compound 1 of Synthesis Example 1. except that 14 g of Intermediate 48 was used instead of Intermediate 2. (Yield 23%, Mass [M+]=956)

Synthesis Example 32. Synthesis of compound 32

12 g of Intermediate 49 was obtained in the same manner as in the preparation of Intermediate 8 of Synthesis Example 5. except that 4.6 g of A-30 was used instead of amine A-5. (Yield 73%, Mass [M+]=592)

13 g of Intermediate 50 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. Except that 12 g of Intermediate 49 was used instead of Intermediate 1 and 7.0 g of A-31 was used instead of amine A-2. (Yield 71%, Mass [M+]=899)

2.9 g of compound 32 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 13 g of Intermediate 50 was used instead of Intermediate 2. (Yield 23%, Mass [M+]=873)

Synthesis Example 33. Synthesis of compound 33

14 g of Intermediate 51 was obtained in the same manner as in the preparation of Intermediate 8 of Synthesis Example 5. except that 8.7 g of A-31 was used instead of amine A-5. (Yield 69%, Mass [M+]=739)

16 g of Intermediate 52 was obtained in the same manner as in the preparation of Intermediate 2 of Synthesis Example 1. except that 14 g of Intermediate 51 was used instead of Intermediate 1. (Yield 76%, Mass [M+]=1108)

3.4 g of compound 33 was obtained in the same manner as in the preparation of compound 1 of Synthesis Example 1. except that 16 g of Intermediate 52 was used instead of Intermediate 2. (Yield 22%, Mass [M+]=1081)

Synthesis Example 34. Synthesis of compound E1

After completely dissolving the compound C-1 (8 g, 27.98 mmol, 1eq.) and the compound I-1 (26.4 g, 58.75 mmol, 2.1eq.) in tetrahydrofuran (80 mL), potassium carbonate (9.7 g , 69.94 mmol, 2.5eq) was added dissolved in 30 mL of water. After adding tetrakistriphenyl-phosphinopalladium (1.0 g, 0.84 mmol), the mixture was heated and stirred for 8 hours. After the reaction was terminated by lowering the temperature to room temperature, the potassium carbonate solution was removed and the white solid was filtered and washed with water and ethanol. The filtered white solid was washed twice with ethyl acetate and hexane, respectively, to prepare compound E1 (15.3 g, yield 71%). MS [M+H]+ = 771

Synthesis Example 35. Synthesis of compound E4

In the same manner as for synthesizing compound E1 of Synthesis Example 34, a compound represented by Formula E4 (16.9 g, yield 77%) was prepared using I-2 (20.8 g) and C-2 (8 g). . MS[M+H] ⁺ =591

Synthesis Example 36. Synthesis of compound E10

In the same manner as for synthesizing compound E1 of Synthesis Example 34, a compound represented by Formula E10 (18.9 g, yield 74%) was prepared using I-3 (24.7 g) and C-2 (8 g). . MS[M+H] ⁺ =691

Synthesis Example 37. Synthesis of compound E2

In the same manner as for synthesizing compound E1 of Synthesis Example 34, the compound represented by Formula E2 (16.8 g, yield 81%) was prepared using I-4 (25.6 g) and C-3 (8 g). . MS[M+H] ⁺ =743

Synthesis Example 38. Synthesis of compound E5

In the same manner as for synthesizing compound E1 of Synthesis Example 34, the compound represented by Formula E5 (14.7 g, yield 78%) was prepared using I-4 (21.8 g) and C-4 (8 g). . MS[M+H] ⁺ =793

Synthesis Example 39. Synthesis of compound E9

In the same manner as for synthesizing compound E1 of Synthesis Example 34, the compound represented by Formula E9 (16.2 g, yield 74%) was prepared using I-2 (20.8 g) and C-5 (8 g). . MS[M+H] ⁺ =793

Synthesis Example 40. Synthesis of compound E3

In the same manner as for synthesizing compound E1 of Synthesis Example 34, a compound represented by the above formula E3 (14.1 g, yield 68%) was prepared using I-5 (25.5 g) and C-6 (8 g). . MS[M+H] ⁺ =741

Synthesis Example 41. Synthesis of Intermediate C-8

The compound C-7 (10 g, 44.83 mmol, 1eq.), potassium carbonate (8.1 g, 58.28 mmol, 1.3eq) and perfluorobutanesulfonyl fluoride (16.3 g, 53.8 mmol, 1.2eq.) was dissolved in 100 mL of acetonitrile and 50 mL of distilled water, followed by stirring at room temperature for 2 hours. After the reaction was completed, acetonitrile was distilled off under reduced pressure, and then 100 mL of acetonitrile and aq. Add 50 mL of NaCl and separate the organic layer using a separatory funnel. The separated organic layer was treated with anhydrous MgSO ₄ and then filtered. The filtered solution was distilled off under reduced pressure and purified by column chromatography (eluent: ethyl acetate/hexane) to obtain Intermediate C-8 (18.3 g, yield 81%).

Synthesis Example 42. Synthesis of compound E8

In the same manner as for synthesizing compound E1 of Synthesis Example 34, a compound represented by Formula E8 (14.1 g, yield 68%) was prepared using I-4 (18.1 g) and C-8 (10 g). . MS[M+H] ⁺ =743

Synthesis Example 43. Synthesis of Intermediate C-10

In the same manner as for synthesizing Intermediate C-8 of Synthesis Example 41, a compound represented by Formula C-10 (23.9 g, yield 77%) was prepared using C-9 (10 g).

Synthesis Example 44. Synthesis of compound E6

In the same manner as for synthesizing compound E1 of Synthesis Example 34, a compound represented by Formula E6 (6.8 g, yield 71%) was prepared using I-5 (8g) and C-10 (10g). MS[M+H] ⁺ =799

Synthesis Example 45. Synthesis of compound E7

In the same manner as for synthesizing compound E1 of Synthesis Example 34, a compound represented by Formula E7 (5.7 g, yield 68%) was prepared using I-7 (6.8 g) and C-10 (10 g). . MS[M+H] ⁺ =699

<Device Example 1>

Example 1

A glass substrate coated with indium tin oxide (ITO) to a thickness of 1000 Å was placed in distilled water in which detergent was dissolved and washed with ultrasonic waves. At this time, 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 washing 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.

A hole injection layer was formed by thermal vacuum deposition of the following HI-A compound to a thickness of 600 Å and the HAT compound to a thickness of 50 Å on the prepared ITO transparent electrode. A hole transport layer was formed by vacuum-depositing 600 Å of the following HT-A compound on the hole injection layer.

Then, the following BH-A compound (host) and compound 2 (dopant) were vacuum-deposited in a weight ratio of 100:2 to a thickness of 200 Å on the hole transport layer to form a light emitting layer.

Compound E1 and the following LiQ compound were vacuum-deposited on the emission layer at a weight ratio of 1:1 to form an electron injection and transport layer to a thickness of 350 Å. By sequentially depositing lithium fluoride (LiF) to a thickness of 10 Å and aluminum to a thickness of 1000 Å on the electron injection and transport layer, A cathode was formed. In the above process, the deposition rate of the organic material was maintained at 0.4 to 0.9 Å/sec, the deposition rate of lithium fluoride of the negative electrode was maintained at 0.3 Å/sec, and the deposition rate of aluminum was maintained at 2 Å/sec, and the vacuum degree during deposition was 1Х10 ^-7 to 5Х10 ^-5 torr, an organic light-emitting device was manufactured.

Examples 2 to 17 and Comparative Examples 1 to 6

An organic light emitting diode was manufactured in the same manner as in Example 1, except that the materials shown in Table 1 below were used for the dopant material of the emission layer and the electron injection and transport layer material.

For the organic light emitting devices of Examples 1 to 17 and Comparative Examples 1 to 6, the driving voltage and luminous efficiency were measured at a current density of 10 mA/cm ² , and 95% of the initial luminance at a current density of 15 mA/cm ² The time (T95) was measured and the results are shown in Table 1 below.

compound 10mA/cm ² 15mA/ ^cm2 dopant electron injection and transport layer Voltage Efficiency (cd/A) T95 (h) Example 1 compound 2 E1 3.69 7.00 123 Example 2 compound 4 E3 3.61 7.06 109 Example 3 compound 5 E4 3.72 7.23 142 Example 4 compound 7 E5 3.53 7.23 106 Example 5 compound 9 E7 3.57 7.17 101 Example 6 compound 11 E8 3.61 7.30 131 Example 7 compound 12 E9 3.69 7.12 133 Example 8 compound 15 E10 3.72 7.00 130 Example 9 compound 17 E2 3.50 7.61 101 Example 10 compound 19 E6 3.50 7.35 105 Example 11 compound 22 E9 3.69 7.18 135 Example 12 compound 23 E10 3.72 7.42 135 Example 13 compound 26 E3 3.61 6.93 111 Example 14 compound 28 E4 3.72 7.11 143 Example 15 compound 30 E5 3.53 7.42 104 Example 16 compound 31 E6 3.50 7.41 102 Example 17 compound 33 E7 3.57 7.80 101 Comparative Example 1 BD-A ET-C 3.80 4.89 91 Comparative Example 2 BD-C ET-B 3.91 4.99 81 Comparative Example 3 BD-A E10 3.65 5.68 116 Comparative Example 4 BD-C E3 3.69 5.95 87 Comparative Example 5 compound 7 ET-B 3.80 5.92 101 Comparative Example 6 compound 22 ET-C 3.91 6.07 102

Referring to Table 1, the low voltage, high efficiency and/or long life characteristics of the organic light emitting device including the compound of Formula 1 of the present invention as a dopant of the light emitting layer and using the compound of Formula 2 of the present invention as an electron injection and transport layer are excellent. Able to know.

<Element example 2>

Example 18

A glass substrate coated with indium tin oxide (ITO) to a thickness of 1000 Å was placed in distilled water in which detergent was dissolved and washed with ultrasonic waves. At this time, 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 washing 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.

A hole injection layer was formed by sequentially thermal vacuum deposition of the HI-A compound to a thickness of 600 Å and the HAT compound to a thickness of 50 Å on the prepared ITO transparent electrode. A hole transport layer was formed by vacuum-depositing 600 Å of the HT-A compound on the hole injection layer. On the hole transport layer, the following HT-B was vacuum deposited to a thickness of 50 Å to form an electron blocking layer.

Subsequently, the BH-B compound (host) and Compound 1 (dopant) were vacuum-deposited in a weight ratio of 100:2 to a thickness of 200 Å on the electron blocking layer to form a light emitting layer.

Compound E1 was vacuum deposited on the light emitting layer to form a hole blocking layer to a thickness of 50 Å. On the hole blocking layer, the following compound ET-D and the LiQ compound were vacuum-deposited in a weight ratio of 1:1 to form an electron injection and transport layer to a thickness of 300 Å. A cathode was formed by sequentially depositing lithium fluoride (LiF) to a thickness of 10 Å and aluminum to a thickness of 1000 Å on the electron injection and transport layer.

In the above process, the deposition rate of the organic material was maintained at 0.4 to 0.9 Å/sec, the deposition rate of lithium fluoride of the negative electrode was maintained at 0.3 Å/sec, and the deposition rate of aluminum was maintained at 2 Å/sec, and the vacuum degree during deposition was 1Х10 ^-7 to 5Х10 ^-5 torr, an organic light-emitting device was manufactured.

Examples 19 to 29 and Comparative Examples 7 to 12

An organic light emitting diode was manufactured in the same manner as in Example 18, except that the materials shown in Table 2 below were used for the dopant material and the hole blocking layer material of the emission layer.

For the organic light emitting devices of Examples 18 to 29 and Comparative Examples 7 to 12, the driving voltage and luminous efficiency were measured at a current density of 10 mA/cm ² , and 95% of the initial luminance at a current density of 15 mA/cm ² The time (T95) was measured and the results are shown in Table 2 below.

compound 10mA/cm ² 15mA/ ^cm2 dopant hole blocking layer Voltage Efficiency (cd/A) T95 (h) Example 18 compound 1 E1 3.69 6.70 119 Example 19 compound 3 E2 3.50 7.29 101 Example 20 compound 8 E3 3.61 6.93 115 Example 21 compound 10 E4 3.72 7.00 148 Example 22 compound 13 E5 3.53 7.23 106 Example 23 compound 18 E6 3.50 7.54 103 Example 24 compound 20 E7 3.57 7.74 101 Example 25 compound 24 E8 3.61 7.23 133 Example 26 compound 25 E10 3.72 6.58 122 Example 27 compound 27 E9 3.69 6.69 127 Example 28 compound 29 E8 3.61 7.42 119 Example 29 compound 32 E1 3.69 7.06 126 Comparative Example 7 BD-A ET-A 3.80 4.94 90 Comparative Example 8 BD-D ET-C 3.61 4.63 75 Comparative Example 9 BD-A E2 3.50 6.13 88 Comparative Example 10 BD-D E4 3.72 5.34 102 Comparative Example 11 compound 1 ET-A 3.80 5.82 97 Comparative Example 12 compound 24 ET-C 3.61 5.9 100

Looking at Table 2, it can be seen that the low voltage, high efficiency and/or long life characteristics of the organic light emitting device including the compound of Formula 1 of the present invention as a dopant of the light emitting layer and using the compound of Formula 2 of the present invention as a hole blocking layer are excellent. can

<Element example 3>

Example 30

A glass substrate coated with indium tin oxide (ITO) to a thickness of 1000 Å was placed in distilled water in which detergent was dissolved and washed with ultrasonic waves. At this time, 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 washing 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.

A hole injection layer was formed by sequentially thermal vacuum deposition of the HI-A compound to a thickness of 600 Å and the HAT compound to a thickness of 50 Å on the prepared ITO transparent electrode. A hole transport layer was formed by vacuum-depositing 600 Å of the HT-A compound on the hole injection layer. The HT-B was vacuum-deposited to a thickness of 50 Å on the hole transport layer to form an electron blocking layer. Then, a BH-C compound (host) and compound 6 (dopant) were vacuum-deposited in a weight ratio of 100:2 to a thickness of 200 Å on the electron blocking layer to form a light emitting layer.

Compound E2 was vacuum deposited on the light emitting layer to form a hole blocking layer to a thickness of 50 Å. Compound E1 and the following LiQ compound were vacuum-deposited on the hole blocking layer at a weight ratio of 1:1 to form an electron injection and transport layer to a thickness of 300 Å. A cathode was formed by sequentially depositing lithium fluoride (LiF) to a thickness of 10 Å and aluminum to a thickness of 1000 Å on the electron injection and transport layer.

In the above process, the deposition rate of the organic material was maintained at 0.4 to 0.9 Å/sec, the deposition rate of lithium fluoride of the negative electrode was maintained at 0.3 Å/sec, and the deposition rate of aluminum was maintained at 2 Å/sec, and the vacuum degree during deposition was 1Х10 ^-7 to 5Х10 ^-5 torr, an organic light-emitting device was manufactured.

Examples 31 to 35 and Comparative Examples 13 to 15

An organic light emitting diode was manufactured in the same manner as in Example 30, except that the materials shown in Table 3 below were used for the dopant material of the emission layer, the hole blocking layer material, and the electron injection and transport layer material.

For the organic light-emitting devices of Examples 30 to 35 and Comparative Examples 13 to 15, the driving voltage and luminous efficiency were measured at a current density of 10 mA/cm ² , and 95% of the initial luminance at a current density of 15 mA/cm ² The time (T95) was measured and the results are shown in Table 3 below.

compound 10mA/cm ² 15mA/ ^cm2 dopant hole blocking layer electron injection and transport layer Voltage Efficiency (cd/A) T95 (h) Example 30 compound 6 E2 E1 3.39 6.94 121 Example 31 compound 14 E3 E9 3.50 7.49 154 Example 32 compound 16 E10 E3 3.54 7.12 146 Example 33 compound 18 E4 E6 3.43 7.54 137 Example 34 compound 21 E9 E7 3.46 7.06 156 Example 35 compound 23 E8 E5 3.36 7.93 125 Comparative Example 13 BD-B ET-B ET-A 3.42 4.94 64 Comparative Example 14 BD-B E2 ET-A 3.69 4.99 86 Comparative Example 15 BD-C ET-B E3 3.42 5.95 89

Referring to Table 3, low voltage, high efficiency and/or of an organic light emitting device including the compound of Formula 1 of the present invention as a dopant of the light emitting layer and using the compound of Formula 2 of the present invention as a hole blocking layer and an electron injection and transport layer It can be seen that the long life characteristics are excellent.

1: substrate / 2: anode / 3: hole injection layer / 4: hole transport layer / 4a: first hole transport layer / 4b: second hole transport layer / 4c: third hole transport layer / 4d: fourth hole transport layer / 4e: second 5 hole transport layer / 4f: sixth hole transport layer / 4p: p-doped hole transport layer / 4R: red hole transport layer / 4G: green hole transport layer / 4B: blue hole transport layer / 5: electron blocking layer / 6: light emitting layer / 6a: First light-emitting layer/6b: second light-emitting layer/ 6c: third light-emitting layer/ 6BF: blue fluorescent light-emitting layer/ 6BFa: first blue fluorescent light-emitting layer/ 6BFb: second blue fluorescent light-emitting layer/ 6YGP: yellow green phosphorescent light-emitting layer/ 6RP: red phosphorescent light-emitting layer / 6GP: green phosphorescent light emitting layer/ 7: hole blocking layer/ 8: electron injection and transport layer/ 9: electron transport layer/ 9a: first electron transport layer/ 9b: second electron transport layer/ 9c: third electron transport layer/ 10: electron injection Layer/ 11: cathode/ 12: N-type charge generation layer/ 12a: first N-type charge generation layer/ 12b: second N-type charge generation layer/ 13: P-type charge generation layer/ 13a: first P-type charge generation Layer/ 13b: second P-type charge generation layer/ 14: capping layer

Claims (12)

a first electrode; a second electrode; and an organic material layer provided between the first electrode and the second electrode,
The organic material layer is an organic light emitting device including a first organic material layer including a compound represented by the following formula (1) and a second organic material layer including a compound represented by the following formula (2):
[Formula 1]

In Formula 1,
A1, A2, A3, B1 and B2 are the same as or different from each other, and each independently represent a hydrocarbon ring;
R1 to R5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; cyano group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted alkynyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted amine group; a substituted or unsubstituted aryl group; a substituted or unsubstituted aryloxy group; Or a substituted or unsubstituted heterocyclic group; Represented by the following formula (3), at least one of R1 to R5 is represented by the following formula (3),
[Formula 3]

The dotted line is a region connected to A1, A2, A3, B1 or B2,
X is C or Si,
R6 to R8 are the same as or different from each other, and are each independently a substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group,
n1 and n5 are each an integer from 0 to 4,
n2 and n4 are each an integer from 0 to 5;
n3 is an integer from 0 to 3,
n1 + n2 + n3 + n4 + n5 is greater than or equal to 1,
When n1 to n5 are 2 or more, the substituents in parentheses are the same as or different from each other,
The formula 3 is represented by the following formula 3-1 or 3-2,
[Formula 3-1]

[Formula 3-2]

In Formulas 3-1 and 3-2,
R11 is a substituted or unsubstituted alkyl group,
R12 is a substituted or unsubstituted aryl group,
R13 is a substituted or unsubstituted alkyl group; Or a substituted or unsubstituted aryl group,
R14 is an alkyl group having 2 to 6 carbon atoms,
R15 is a substituted or unsubstituted aryl group,
R16 is an alkyl group having 2 to 6 carbon atoms; Or a substituted or unsubstituted aryl group,
[Formula 2]

In Formula 2,
At least one of X1 to X3 is N, and the rest are each independently N or CH,
L is a direct bond; Or a substituted or unsubstituted arylene group,
Ar5 and Ar6 are the same as or different from each other, and each independently a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group,
Ar7 is a substituted or unsubstituted m-valent aryl group; Or a substituted or unsubstituted m is a cycloalkyl group,
m is an integer of 2 to 4, and when m is 2 or more, two or more substituents in parentheses are the same as or different from each other. delete The organic light emitting diode of claim 1, wherein Chemical Formula 1 is represented by Chemical Formula 1-1:
[Formula 1-1]

In Formula 1-1, R1 to R5 and n1 to n5 are as defined in Formula 1 above. The method according to claim 1,
R1, R2, R4, and R5 are the same as or different from each other, and each independently represent hydrogen; heavy hydrogen; halogen group; cyano group; an alkyl group having 1 to 10 carbon atoms that is unsubstituted or substituted with deuterium; a cycloalkyl group having 3 to 30 carbon atoms that is unsubstituted or substituted with deuterium; an arylamine group having 6 to 60 carbon atoms that is unsubstituted or substituted with deuterium; an aryl group having 6 to 30 carbon atoms, unsubstituted or substituted with one or more substituents selected from the group consisting of deuterium, a halogen group, a cyano group, and an alkyl group having 1 to 10 carbon atoms, or a substituent to which two or more groups selected from the group are connected; a heterocyclic group having 2 to 30 carbon atoms that is unsubstituted or substituted with deuterium; Or represented by the above formula (3),
R3 is hydrogen; heavy hydrogen; halogen group; cyano group; an alkyl group having 1 to 10 carbon atoms that is unsubstituted or substituted with deuterium; a cycloalkyl group having 3 to 30 carbon atoms that is unsubstituted or substituted with deuterium; At least one substituent selected from the group consisting of deuterium, a halogen group, a cyano group, an alkyl group having 1 to 10 carbon atoms, an aryl group having 6 to 30 carbon atoms, and a silyl group, or a substituent selected from the group consisting of two or more groups selected from the group consisting of a substituted or unsubstituted C6 to 60 arylamine groups; an aryl group having 6 to 30 carbon atoms that is unsubstituted or substituted with deuterium, a halogen group, or a cyano group; a heterocyclic group having 2 to 30 carbon atoms that is unsubstituted or substituted with deuterium; Or an organic light emitting device represented by the formula (3). The method according to claim 1,
Formula 2 is an organic light emitting device represented by the following Formula 2-1:
[Formula 2-1]

In Formula 2-1,
X1 to X3, L, Ar5 and Ar6 are as defined in Formula 2 above,
L' is a direct bond; Or a substituted or unsubstituted arylene group,
At least one of X1' to X3' is N, and the rest are each independently N or CH,
Ar5' and Ar6' are the same as or different from each other, and are each independently a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group,
Ar7' is a substituted or unsubstituted arylene group; or a substituted or unsubstituted cycloalkylene group. 6. The method of claim 5,
Ar7' is any one selected from the following structure organic light emitting device:

. The organic light-emitting device according to claim 1, wherein the compound represented by Formula 1 is any one selected from the following compounds:

. The organic light-emitting device according to claim 1, wherein the compound represented by Formula 2 is any one selected from the following compounds:

. The method according to claim 1,
The first electrode is an anode, the second electrode is a cathode, the first organic material layer is a light emitting layer, and the second organic material layer is provided between the second electrode and the first organic material layer. The method according to claim 1,
The organic material layer includes two or more light emitting layers, and one of the two or more light emitting layers includes the compound represented by Formula 1 above. The method according to claim 1,
The second organic material layer is an organic light emitting device further comprising one or more n-type dopants selected from alkali metals and alkaline earth metals. The method according to claim 1,
The second organic material layer is an organic light emitting device comprising at least one layer selected from the group consisting of a hole blocking layer, an electron transport layer, an electron injection layer, and an electron injection and transport layer.

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