KR20240048945A - Compound and organic light emitting device comprising the same - Google Patents

Abstract

This specification relates to the compound of Formula 1 and an organic light-emitting device containing the same.

Description

Compound and organic light-emitting device containing the same {COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME}

This specification relates to compounds and organic light-emitting devices containing the same.

In this specification, an organic light-emitting device is a light-emitting device using an organic semiconductor material and requires exchange of holes and/or electrons between an electrode and an organic semiconductor material. Organic light-emitting devices can be broadly divided into two types according to their operating principles as follows. First, excitons are formed in the organic layer by photons flowing into the device from an external light source, these excitons are separated into electrons and holes, and these electrons and holes are transferred to different electrodes and used as current sources (voltage sources). It is a type of light emitting device. The second type is a light-emitting device that applies voltage or current to two or more electrodes to inject holes and/or electrons into the organic semiconductor material layer forming the interface with the electrodes, and operates by the injected electrons and holes.

In general, organic luminescence refers to a phenomenon that converts electrical energy into light energy using organic materials. Organic light-emitting devices that utilize the organic light-emitting phenomenon usually have a structure including an anode, a cathode, and an organic material layer between them. Here, the organic material layer is often composed of a multi-layer structure composed of different materials to increase the efficiency and stability of the organic light-emitting device, and for example, it consists of a hole injection layer, a hole transport layer, a light-emitting layer, an electron suppression layer, an electron transport layer, and an electron injection layer. You can lose. In the structure of this organic light-emitting device, when a voltage is applied between the two electrodes, holes are injected from the anode and electrons from the cathode into the organic material layer. When the injected holes and electrons meet, an exciton is formed, and this exciton When it falls back to the ground state, it glows. These organic light-emitting devices are known to have characteristics such as self-luminescence, high brightness, high efficiency, low driving voltage, wide viewing angle, and high contrast.

Materials used as organic layers in organic light-emitting devices can be classified into light-emitting materials and charge transport materials, such as hole injection materials, hole transport materials, electron suppression materials, electron transport materials, and electron injection materials, depending on their function. Depending on the color of light emitting, there are blue, green, and red light emitting materials, and yellow and orange light emitting materials needed to realize better natural colors.

Additionally, in order to increase color purity and increase luminous efficiency through energy transfer, a host/dopant system can be used as a luminescent material. The principle is that when a small amount of dopant, which has a smaller energy band gap and higher luminous efficiency than the host that mainly constitutes the light-emitting layer, is mixed into the light-emitting layer, excitons generated in the host are transported to the dopant, producing highly efficient light. At this time, since the wavelength of the host moves to the wavelength of the dopant, light of the desired wavelength can be obtained depending on the type of dopant used.

In order to fully demonstrate the excellent characteristics of the above-described organic light-emitting device, the materials that make up the organic layer within the device, such as hole injection material, hole transport material, light-emitting material, electron suppressor material, electron transport material, and electron injection material, must be stable and efficient materials. As it is supported by , the development of new materials continues to be required.

International Patent Publication No. 2017-126443

Compounds and organic light-emitting devices containing the same are described herein.

An exemplary embodiment of the present specification provides a compound of Formula 1 below.

[Formula 1]

In Formula 1,

R1, and R3 to R8 are the same or different from each other and are each independently hydrogen or deuterium,

R2 is a substituted or unsubstituted alkyl group, or a substituted or unsubstituted cycloalkyl group,

L1 and L2 are the same or different from each other and are each independently a direct bond, a substituted or unsubstituted arylene group, or a substituted or unsubstituted heteroarylene group,

At least one of A1 and A2 is of the following formula A-1 or A-2, and the remainder is a substituted or unsubstituted hydrocarbon ring group, or a substituted or unsubstituted 3- or 4-ring heteroaryl containing N, O, or S. It's awesome,

[Formula A-1]

[Formula A-2]

In the above formulas A-1 and A-2,

R9 and R10 are the same or different from each other, and are each independently hydrogen, deuterium, a halogen group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted group. It is a heteroaryl group,

R11 or R12 is a site that binds to L1 or L2,

R15 or R16 is a site that binds to L1 or L2,

A substituent among R11, R12, R15 and R16 that does not bind to L1 or L2; R13, R14, R17, and R8 are the same as or different from each other, and are each independently hydrogen, deuterium, a halogen group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted aryl group, or It is a substituted or unsubstituted heteroaryl group,

X1 is O or S,

a and b are each integers from 1 to 6,

When a is 2 or more, R9 is the same or different from each other,

When b is 2 or more, R10 is the same or different from each other.

Additionally, according to an exemplary embodiment of the present invention, a first electrode; a second electrode provided opposite the first electrode; and an organic light-emitting device including one or more organic material layers provided between the first electrode and the second electrode, wherein one or more layers of the organic material layers include the above-mentioned compounds.

The compound of the present invention can be used as a material for the organic layer of an organic light-emitting device. When manufacturing an organic light-emitting device including the compound of the present invention, an organic light-emitting device with high efficiency, low voltage, and long lifespan characteristics can be obtained, and when the compound of the present invention is included in the electron transport layer of the organic light-emitting device, intramolecular Due to its high polarity, the effect of electron transfer is high, making it possible to manufacture organic light-emitting devices with long-life characteristics.

Specifically, the compounds described in this specification have an alkyl group or cycloalkyl group (R2) with electron donating ability bonded to the 2nd carbon position of anthracene, and therefore have a high HOMO (highest occupied molecular orbital) level, thereby forming a hole in the device. Injection characteristics can be improved, and since a substituent with excellent electron transfer is attached to the 9th or 10th carbon position of anthracene, electron injection and transport within the device can be improved.

1 and 2 show examples of organic light-emitting devices according to the present invention.

Hereinafter, this specification will be described in more detail.

In this specification, when a part “includes” a certain component, this means that it may further include other components rather than excluding other components, unless specifically stated to the contrary.

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

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

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

As used herein, the term “substituted or unsubstituted” refers to deuterium; halogen group; Cyano group (-CN); silyl group; boron group; Substituted or unsubstituted alkyl group; Substituted or unsubstituted cycloalkyl group; Substituted or unsubstituted aryl group; and substituted or unsubstituted heterocyclic groups, or is substituted with a substituent in which two or more of the above-exemplified substituents are linked, or does not have any substituent. For example, “a substituent group in which two or more substituents are connected” may be a biphenyl group. That is, the biphenyl group may be an aryl group, or it may be interpreted as a substituent in which two phenyl groups are connected.

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

In this specification, examples of halogen groups include fluorine (F), chlorine (Cl), bromine (Br), or iodine (I).

In the present specification, the silyl group is deuterium; Substituted or unsubstituted alkyl group; Alternatively, it may be substituted or unsubstituted with a substituted or unsubstituted aryl group. The silyl group specifically includes, but is not limited to, trimethylsilyl group, triethylsilyl group, t-butyldimethylsilyl group, vinyldimethylsilyl group, propyldimethylsilyl group, triphenylsilyl group, diphenylsilyl group, and phenylsilyl group. No.

In this specification, the boron group is deuterium; Substituted or unsubstituted alkyl group; Alternatively, it may be substituted or unsubstituted with a substituted or unsubstituted aryl group. The boron group specifically includes, but is not limited to, trimethyl boron group, triethyl boron group, t-butyldimethyl boron group, triphenyl boron group, and phenyl boron group.

In the present specification, the alkyl group may be straight chain or branched, and the number of carbon atoms is not particularly limited, but is preferably 1 to 60. According to one embodiment, the carbon number of the alkyl group is 1 to 30. According to another embodiment, the carbon number of the alkyl group is 1 to 20. According to another embodiment, the carbon number of the alkyl group is 1 to 10. Specific examples of alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, hexyl, heptyl, and octyl groups.

In this specification, the amine group is -NH ₂ ; Alkylamine group; N-alkylarylamine group; Arylamine group; N-arylheteroarylamine group; It may be selected from the group consisting of N-alkylheteroarylamine group and heteroarylamine group, and the number of carbon atoms is not particularly limited, but is preferably 1 to 30. Specific examples of amine groups include methylamine groups; dimethylamine group; ethylamine group; diethylamine group; phenylamine group; Naphthylamine group; Biphenylamine group; Anthracenylamine group; 9-methylanthracenylamine group; Diphenylamine group; Ditolylamine group; N-phenyltolylamine group; Triphenylamine group; N-phenylbiphenylamine group; N-phenylnaphthylamine group; N-biphenylnaphthylamine group; N-naphthylfluorenylamine group; N-phenylphenanthrenylamine group; N-biphenylphenanthrenylamine group; N-phenylfluorenylamine group; N-phenylterphenylamine group; N-phenanthrenylfluorenylamine group; N-biphenylfluorenylamine group, etc., but is not limited thereto.

In the present specification, N-alkylarylamine group refers to an amine group in which the N of the amine group is substituted with an alkyl group and an aryl group.

In the present specification, N-arylheteroarylamine group refers to an amine group in which the N of the amine group is substituted with an aryl group and a heteroaryl group.

In the present specification, N-alkylheteroarylamine group refers to an amine group in which the N of the amine group is substituted with an alkyl group and a heteroaryl group.

In this specification, the alkyl groups in the alkylamine group, N-arylalkylamine group, alkylthioxy group, alkylsulfoxy group, and N-alkylheteroarylamine group are the same as examples of the alkyl groups described above. Specifically, the alkylthioxy group includes methylthioxy group; ethylthioxy group; tert-butylthioxy group; hexylthioxy group; Octylthioxy groups, etc., and examples of alkylsulfoxy groups include mesyl; ethyl sulfoxy group; Propyl alcohol oxygen group; butyl sulfoxy group, etc., but is not limited thereto.

In the present specification, the cycloalkyl group is not particularly limited, but preferably has 3 to 60 carbon atoms, and according to one embodiment, the cycloalkyl group has 3 to 30 carbon atoms. According to another embodiment, the carbon number of the cycloalkyl group is 3 to 20. According to another embodiment, the carbon number of the cycloalkyl group is 3 to 6. Specifically, it includes cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group, etc., but is not limited thereto.

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

In the present specification, the heteroaryl group is a cyclic group containing one or more of N, O, P, S, Si, and Se as heteroatoms, and the number of carbon atoms is not particularly limited, but it is preferably 2 to 60 carbon atoms. According to one embodiment, the carbon number of the heterocyclic group is 2 to 30. Examples of heterocyclic groups include pyridine group, pyrrole group, pyrimidine group, pyridazinyl group, furan group, thiophene group, imidazole group, pyrazole group, dibenzofuran group, dibenzothiophene group, carbazole group, etc. However, it is not limited to these.

In the present specification, hydrocarbon ring refers to an aliphatic ring group, an aromatic ring group, and a ring group in which aliphatic and aromatic rings are condensed with each other.

In the present specification, the definition of a cycloalkyl group may be applied to the aliphatic ring group.

In the present specification, the definition of an aryl group may be applied to the aromatic ring group.

In this specification, the arylene group is the same as defined for the aryl group above, except that it is a divalent group.

In the present specification, the heteroarylene group is the same as defined for the heteroaryl group above, except that it is a divalent group.

In the present specification, Formula A1 is one of the structures below.

In the present specification, Formula A2 is one of the structures below.

In the above structure, either carbon is bonded to L1 or L2 of Formula 1.

In the present specification, the formula X1 is O.

In this specification, the formula X1 is S.

In this specification, Formula 1 is the following Formula 1-1 or 1-2.

[Formula 1-1] [Formula 1-2]

In Formulas 1-1 and 1-2, R1 to R9, R11 to R14, L1, L2, X1, A2, and a are as defined in Formulas 1 and A-1.

In this specification, Formula 1 is the following Formula 1-3 or 1-4.

[Formula 1-3] [Formula 1-4]

In Formulas 1-3 and 1-4, R1 to R8, R10, R15 to R18, L1, L2, X1, A2, and b are as defined in Formulas 1 and A-2.

In this specification, Formula 1 is Formula 2-1 or 2-2 below.

[Formula 2-1] [Formula 2-2]

In Formula 2-1 or 2-2, R1 to R9, R11 to R14, L1, L2, X1, A1 and a are as defined in Formula 1 and A-1.

In the present specification, Formula 1 is the following Formula 2-3 or 2-4.

[Formula 2-3] [Formula 2-4]

In Formulas 2-3 and 2-4, R1 to R8, R10, R15 to R18, L1, L2, X1, A2 and b are as defined in Formulas 1 and A-2.

According to an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and are each independently a direct bond, a substituted or unsubstituted arylene having 6 to 30 carbon atoms, or a substituted or unsubstituted arylene having 3 to 30 carbon atoms. It is a heteroarylene group.

According to an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and are each independently a direct bond, a substituted or unsubstituted arylene having 6 to 20 carbon atoms, or a substituted or unsubstituted arylene having 3 to 20 carbon atoms. It is a heteroarylene group.

According to an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and are each independently a direct bond, a substituted or unsubstituted arylene having 6 to 15 carbon atoms, or a substituted or unsubstituted arylene having 3 to 15 carbon atoms. It is a heteroarylene group.

According to an exemplary embodiment of the present specification, L1 and L2 are the same or different from each other, and are each independently a direct bond, a phenylene group, a divalent unsubstituted biphenyl group, a divalent unsubstituted terphenyl group, and a divalent unsubstituted group. naphthyl group, divalent unsubstituted anthracene group, divalent unsubstituted phenanthrene group, divalent unsubstituted pyrene group, divalent carbazole group, divalent pyridine group, divalent pyrimidine group, divalent triazine group, It is a divalent dibenzofuran group, a divalent dibenzothiophene group, a divalent furan group, a divalent thiophene group, a divalent benzofuran group, a divalent benzimidazole group, or a divalent benzoxazole group,

The substituents are substituted or unsubstituted with deuterium, an alkyl group with 1 to 10 carbon atoms, or an aryl group with 6 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, L1 and L2 are the same or different from each other, and are each independently a direct bond, a phenylene group, a divalent unsubstituted biphenyl group, a divalent unsubstituted terphenyl group, and a divalent unsubstituted group. naphthyl group, divalent unsubstituted anthracene group, divalent unsubstituted phenanthrene group, divalent unsubstituted pyrene group, divalent carbazole group, divalent pyridine group, divalent pyrimidine group, divalent triazine group, It is a divalent dibenzofuran group, a divalent dibenzothiophene group, a divalent furan group, a divalent thiophene group, a divalent benzofuran group, a divalent benzimidazole group, or a divalent benzoxazole group,

The substituents are substituted or unsubstituted with deuterium, an alkyl group with 1 to 6 carbon atoms, or an aryl group with 6 to 20 carbon atoms.

According to an exemplary embodiment of the present specification, L1 and L2 are the same or different from each other, and are each independently a direct bond, a phenylene group, a divalent unsubstituted biphenyl group, a divalent unsubstituted terphenyl group, and a divalent unsubstituted group. naphthyl group, divalent unsubstituted anthracene group, divalent unsubstituted phenanthrene group, divalent unsubstituted pyrene group, divalent carbazole group, divalent pyridine group, divalent pyrimidine group, divalent triazine group, It is a divalent dibenzofuran group, a divalent dibenzothiophene group, a divalent furan group, a divalent thiophene group, a divalent benzofuran group, a divalent benzimidazole group, or a divalent benzoxazole group,

The substituents are substituted or unsubstituted with deuterium, methyl group, terbutyl group, phenyl group, or naphthyl group.

According to an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and are each independently a direct bond, an unsubstituted arylene group with 6 to 30 carbon atoms, or a heteroarylene group with 3 to 30 carbon atoms.

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

According to an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and are each independently a direct bond, an unsubstituted arylene group having 6 to 20 carbon atoms, or a heteroarylene group having 3 to 20 carbon atoms.

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

According to an exemplary embodiment of the present specification, L1 and L2 are the same or different from each other, and are each independently a direct bond, an unsubstituted phenylene group, a divalent unsubstituted biphenyl group, a divalent unsubstituted terphenyl group, 2 A divalent unsubstituted naphthyl group, a divalent unsubstituted anthracene group, a divalent unsubstituted phenanthrene group, a divalent unsubstituted pyrene group, a divalent carbazole group, a divalent pyridine group, a divalent pyrimidine group, a divalent It is a triazine group, a divalent dibenzofuran group, a dibenzothiophene group, a divalent furan group, a divalent thiophene group, a divalent benzimidazole, or a divalent benzoxazole.

According to an exemplary embodiment of the present specification, L1 and L2 are the same or different from each other, and are each independently a direct bond, an unsubstituted phenylene group, a divalent unsubstituted biphenyl group, a divalent unsubstituted naphthyl group, 2 It is a divalent unsubstituted terphenyl group, a divalent unsubstituted pyrene group, or a divalent unsubstituted triphenylene group.

According to an exemplary embodiment of the present specification, L1 and L2 are the same or different from each other, and are each independently a direct bond, an unsubstituted phenylene group, a divalent unsubstituted biphenyl group, a divalent unsubstituted naphthyl group, or It is a divalent unsubstituted terphenyl group.

According to an exemplary embodiment of the present specification, L1 and L2 are the same or different from each other and are each independently a direct bond.

According to an exemplary embodiment of the present specification, L1 and L2 are the same or different from each other, and each independently represents an unsubstituted phenylene group.

According to an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently represents a divalent unsubstituted naphthyl group.

According to an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently represents a divalent unsubstituted biphenyl group.

According to an exemplary embodiment of the present specification, L1 and L2 are the same as or different from each other, and each independently represents a divalent unsubstituted terphenyl group.

According to an exemplary embodiment of the present specification, L1 is a direct bond.

According to an exemplary embodiment of the present specification, L1 is an unsubstituted phenylene group.

According to an exemplary embodiment of the present specification, L1 is a divalent unsubstituted naphthyl group.

According to an exemplary embodiment of the present specification, L1 is a divalent unsubstituted biphenyl group.

According to an exemplary embodiment of the present specification, L1 is a divalent unsubstituted terphenyl group.

According to an exemplary embodiment of the present specification, L2 is a direct bond.

According to an exemplary embodiment of the present specification, L2 is an unsubstituted phenylene group.

According to an exemplary embodiment of the present specification, L2 is a divalent unsubstituted naphthyl group.

According to an exemplary embodiment of the present specification, L2 is a divalent unsubstituted biphenyl group.

According to an exemplary embodiment of the present specification, L2 is a divalent unsubstituted terphenyl group.

According to an exemplary embodiment of the present specification, the substituent other than Formula 2-1 or 2-2 among A1 and A2 is a substituted or unsubstituted hydrocarbon ring group having 6 to 30 carbon atoms; Or it is a substituted or unsubstituted 3- or 4-ring heteroaryl group containing N, O or S and having 3 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, the substituent other than Formula 2-1 or 2-2 among A1 and A2 is a substituted or unsubstituted hydrocarbon ring group having 6 to 20 carbon atoms; or a substituted or unsubstituted 3- or 4-ring heteroaryl group containing N, O or S and having 3 to 20 carbon atoms.

According to an exemplary embodiment of the present specification, the substituent other than Formula 2-1 or 2-2 among A1 and A2 is a substituted or unsubstituted hydrocarbon ring group having 6 to 18 carbon atoms; or a substituted or unsubstituted 3- or 4-ring heteroaryl group containing N, O or S and having 3 to 18 carbon atoms.

According to an exemplary embodiment of the present specification, the substituents other than Formula 2-1 or 2-2 among A1 and A2 are substituted or provided with one or more of deuterium, an alkyl group having 1 to 10 carbon atoms, and an aryl group having 6 to 30 carbon atoms. A limited hydrocarbon ring group having 6 to 30 carbon atoms; or a tricyclic or tetracyclic heteroaryl group having 3 to 30 carbon atoms containing N, O or S substituted or unsubstituted with one or more of deuterium, an alkyl group with 1 to 10 carbon atoms, and an aryl group with 6 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, the substituents other than Formula 2-1 or 2-2 among A1 and A2 are substituted or provided with one or more of deuterium, an alkyl group having 1 to 10 carbon atoms, and an aryl group having 6 to 30 carbon atoms. A limited hydrocarbon ring group having 6 to 20 carbon atoms; or a tricyclic or tetracyclic heteroaryl group having 3 to 30 carbon atoms containing N, O or S substituted or unsubstituted with one or more of deuterium, an alkyl group with 1 to 10 carbon atoms, and an aryl group with 6 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, the substituents other than Formula 2-1 or 2-2 among A1 and A2 are tetrahydronaphthalene group, phenyl group, naphthyl group, biphenyl group, terphenyl group, phenanthrene group, and benzophenanthrene group. , triphenylene group, fluoranthene group, pyrene group, fluorene group, dibenzofuran group, dibenzothiophene group, benzonaphthofuran group, benzonaphthothiophene group, or carbazole group,

The substituent is substituted or unsubstituted with deuterium, an alkyl group with 1 to 10 carbon atoms, or an aryl group with 6 to 20 carbon atoms.

According to an exemplary embodiment of the present specification, A1 has the formula A-1.

According to an exemplary embodiment of the present specification, A2 is Formula A-1.

According to an exemplary embodiment of the present specification, A1 has the formula A-2.

According to an exemplary embodiment of the present specification, A2 has the formula A-2.

According to an exemplary embodiment of the present specification, A1 is Formula A-1, and A2 is Formula A-2.

According to an exemplary embodiment of the present specification, A1 is Formula A-2, and A2 is Formula A-1.

According to an exemplary embodiment of the present specification, A1 and A2 are of formula A-1.

According to an exemplary embodiment of the present specification, A1 and A2 are of formula A-2.

According to an exemplary embodiment of the present specification, A1 has the formula A-1, and A2 has 6 to 30 carbon atoms substituted or unsubstituted with one or more of deuterium, an alkyl group with 1 to 10 carbon atoms, and an aryl group with 6 to 20 carbon atoms. It is an aryl group of

According to an exemplary embodiment of the present specification, A1 has the formula A-2, and A2 has 6 to 30 carbon atoms substituted or unsubstituted with one or more of deuterium, an alkyl group with 1 to 10 carbon atoms, and an aryl group with 6 to 20 carbon atoms. It is an aryl group of

According to an exemplary embodiment of the present specification, A2 has the formula A-1, and A1 is a group of 6 to 30 carbon atoms substituted or unsubstituted with one or more of deuterium, an alkyl group with 1 to 10 carbon atoms, and an aryl group with 6 to 20 carbon atoms. It is an aryl group of

According to an exemplary embodiment of the present specification, A2 has the formula A-2, and A1 has 6 to 30 carbon atoms substituted or unsubstituted with one or more of deuterium, an alkyl group with 1 to 10 carbon atoms, and an aryl group with 6 to 20 carbon atoms. It is an aryl group of

According to an exemplary embodiment of the present specification, A1 has the formula A-1, and A2 has 6 to 30 carbon atoms substituted or unsubstituted with one or more of deuterium, an alkyl group with 1 to 10 carbon atoms, and an aryl group with 6 to 20 carbon atoms. It is a hydrocarbon ring group.

According to an exemplary embodiment of the present specification, A1 has the formula A-2, and A2 has 6 to 30 carbon atoms substituted or unsubstituted with one or more of deuterium, an alkyl group with 1 to 10 carbon atoms, and an aryl group with 6 to 20 carbon atoms. It is a hydrocarbon ring group.

According to an exemplary embodiment of the present specification, A2 has the formula A-1, and A1 is a group of 6 to 30 carbon atoms substituted or unsubstituted with one or more of deuterium, an alkyl group with 1 to 10 carbon atoms, and an aryl group with 6 to 20 carbon atoms. It is a hydrocarbon ring group.

According to an exemplary embodiment of the present specification, A2 has the formula A-2, and A1 has 6 to 30 carbon atoms substituted or unsubstituted with one or more of deuterium, an alkyl group with 1 to 10 carbon atoms, and an aryl group with 6 to 20 carbon atoms. It is a hydrocarbon ring group.

According to an exemplary embodiment of the present specification, A1 is Formula A-1, and A2 is N, O or It is a 3- or 4-ring heteroaryl group containing S and having 3 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, A1 is of the formula A-2, and A2 is N, O or It is a 3- or 4-ring heteroaryl group containing S and having 3 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, A2 is Formula A-1, and A1 is N, O or It is a 3- or 4-ring heteroaryl group containing S and having 3 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, A2 has the formula A-2, and A1 is N, O or It is a 3- or 4-ring heteroaryl group containing S and having 3 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, R2 is a substituted or unsubstituted alkyl group, or a substituted or unsubstituted cycloalkyl group.

According to an exemplary embodiment of the present specification, R2 is a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms, or a substituted or unsubstituted cycloalkyl group having 3 to 10 carbon atoms.

According to an exemplary embodiment of the present specification, R2 is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or a substituted or unsubstituted cycloalkyl group having 3 to 6 carbon atoms.

According to an exemplary embodiment of the present specification, R2 is an alkyl group having 1 to 10 carbon atoms unsubstituted or substituted with deuterium or an alkyl group having 1 to 10 carbon atoms; or a cycloalkyl group having 3 to 10 carbon atoms that is substituted or unsubstituted with deuterium or an alkyl group having 1 to 10 carbon atoms.

According to an exemplary embodiment of the present specification, R2 is an alkyl group with 1 to 6 carbon atoms substituted or unsubstituted with deuterium or an alkyl group with 1 to 10 carbon atoms, or an alkyl group with 3 carbon atoms substituted or unsubstituted with deuterium or an alkyl group with 1 to 10 carbon atoms. It is a cycloalkyl group of 6 to 6.

According to an exemplary embodiment of the present specification, R2 is a methyl group substituted or unsubstituted with deuterium, a terbutyl group substituted or unsubstituted with deuterium, an isopropyl group substituted or unsubstituted with deuterium, or a methyl group substituted or unsubstituted with deuterium. Cyclopentyl group, cyclohexyl group substituted or unsubstituted with deuterium, adamantyl group substituted or unsubstituted with deuterium, cyclopentyl group substituted with an alkyl group, cyclohexyl group substituted with an alkyl group, or adamantyl group substituted with an alkyl group. am.

According to an exemplary embodiment of the present specification, R2 is a methyl group unsubstituted or substituted with deuterium; Terbutyl group substituted or unsubstituted with deuterium; Isopropyl group substituted or unsubstituted with deuterium; Cyclopentyl group substituted or unsubstituted with deuterium; Cyclohexyl group substituted or unsubstituted with deuterium; Adamantyl group substituted or unsubstituted with deuterium; Cyclopentyl group substituted with an alkyl group having 1 to 10 carbon atoms; Cyclohexyl group substituted with an alkyl group having 1 to 10 carbon atoms; Or it is an adamantyl group substituted with an alkyl group having 1 to 10 carbon atoms.

According to an exemplary embodiment of the present specification, R2 is a methyl group unsubstituted or substituted with deuterium; Terbutyl group substituted or unsubstituted with deuterium; Isopropyl group substituted or unsubstituted with deuterium; Cyclopentyl group substituted or unsubstituted with deuterium; Cyclohexyl group substituted or unsubstituted with deuterium; Adamantyl group substituted or unsubstituted with deuterium; Cyclopentyl group substituted with methyl group; Cyclohexyl group substituted with methyl group; Or it is an adamantyl group substituted with a methyl group.

According to an exemplary embodiment of the present specification, R1, and R3 to R8 are hydrogen.

According to an exemplary embodiment of the present specification, R1, and R3 to R8 are deuterium.

According to an exemplary embodiment of the present specification, one of R1, and R3 to R8 is deuterium, and the remainder is hydrogen.

According to an exemplary embodiment of the present specification, any two of R1 and R3 to R8 are deuterium, and the remainder is hydrogen.

According to an exemplary embodiment of the present specification, any three of R1 and R3 to R8 are deuterium, and the remainder are hydrogen.

According to an exemplary embodiment of the present specification, any four of R1 and R3 to R8 are deuterium, and the remainder are hydrogen.

According to an exemplary embodiment of the present specification, any five of R1, and R3 to R8 are deuterium, and the remainder are hydrogen.

According to an exemplary embodiment of the present specification, any six of R1, and R3 to R8 are deuterium, and the remainder are hydrogen.

According to an exemplary embodiment of the present specification, more than 10% of the substitutable positions in Formula 1 are substituted with deuterium.

According to an exemplary embodiment of the present specification, more than 15% of the substitutable positions in Formula 1 are substituted with deuterium.

According to an exemplary embodiment of the present specification, more than 20% of the substitutable positions in Formula 1 are substituted with deuterium.

According to an exemplary embodiment of the present specification, more than 25% of the substitutable positions in Formula 1 are substituted with deuterium.

According to an exemplary embodiment of the present specification, more than 30% of the substitutable positions in Formula 1 are substituted with deuterium.

According to an exemplary embodiment of the present specification, more than 35% of the substitutable positions in Formula 1 are substituted with deuterium.

According to an exemplary embodiment of the present specification, more than 40% of the substitutable positions in Formula 1 are substituted with deuterium.

According to an exemplary embodiment of the present specification, more than 45% of the substitutable positions in Formula 1 are substituted with deuterium.

According to an exemplary embodiment of the present specification, Formula 1 is one of the structural formulas below.

Substituents of the compound of Formula 1 may be combined by methods known in the art, and the type, position, or number of substituents may be changed according to techniques known in the art.

In addition, by introducing various substituents into the core structure of the above structure, it is possible to synthesize compounds having the unique properties of the introduced substituents. For example, by introducing substituents mainly used in hole injection layer materials, hole transport materials, light emitting layer materials, and electron transport layer materials used in the manufacture of organic light-emitting devices into the core structure, a material that satisfies the conditions required for each organic material layer can be synthesized. You can.

In the organic light-emitting device according to an exemplary embodiment of the present specification, the deuterium substitution rate for the compound represented by Formula 1 is independently 1% or more and 100% or less.

In an exemplary embodiment of the present specification, the deuterium substitution rate for the compound represented by Formula 1 may each independently be 1% or more, 10% or more, 20% or more, 30% or more, 40% or more, or 50% or more. .

In an exemplary embodiment of the present specification, the deuterium substitution rate for the compound represented by Formula 1 may each independently be 100% or less, 99% or less, 98% or less, 97% or less, 96% or less, or 95% or less. .

In an exemplary embodiment of the present specification, the deuterium substitution rate for the compound represented by Formula 1 is all 100%.

The deuterium substitution rate can be calculated by the method described above. According to a further example, at least one deuterium is substituted directly on the anthracene of Formula 1 above. The light-emitting layer of an organic light-emitting device is a region that emits light and is a section in which molecular loss due to energy is large. The carbon-deuterium bond is stronger than the carbon-hydrogen bond, and since deuterium has a higher mass value than hydrogen, the zero point energy with carbon is lowered and the bond energy is high, so the molecule of the compound of formula 2 By replacing the carbon-hydrogen bonds contained within with carbon-deuterium bonds, the bond energy of the molecule can be increased to obtain a device with excellent lifespan.

Zero point energy =

An organic light emitting device containing a compound of Formula 1 and/or Formula 2 having a deuterium substitution rate according to an exemplary embodiment of the present specification has improved heat resistance and improved lifespan.

As used herein, “deuterated” or “deuterated” means that hydrogen at a replaceable position in a compound is replaced with deuterium.

As used herein, “perdeuterated” means a compound or group in which all hydrogens in the molecule are substituted or unsubstituted with deuterium, and has the same meaning as “100% deuterated.”

As used herein, “X% deuterated”, “Deuteration degree X%”, or “Deuterium substitution rate X%” means that For example, when the structure in question is dibenzofuran, the dibenzofuran is “25% deuterated,” the “deuteration degree of 25%” of the dibenzofuran, or the “deuterium substitution rate of 25%” of the dibenzofugan is as described above. This means that two of the eight hydrogens at the replaceable positions of dibenzofuran are substituted or unsubstituted with deuterium.

In this specification, “deuteration degree” or “deuterium substitution rate” refers to nuclear magnetic resonance spectroscopy (1H NMR), TLC/MS (Thin-Layer Chromatography/Mass Spectrometry), or GC/MS (Gas Chromatography/Mass Spectrometry). This can be confirmed using publicly known methods.

Specifically, when analyzing the "degree of deuteration" or "deuterium substitution rate" by nuclear magnetic resonance spectroscopy (1H NMR), DMF (dimethylformamide) is added as an internal standard, and through the integration rate on 1H NMR, The degree of deuteration or deuterium substitution rate can be calculated from the integrated amount of the total peak.

In addition, when analyzing the “degree of deuteration” or “deuterium substitution rate” through TLC/MS (Thin-Layer Chromatography/Mass Spectrometry), the substitution rate is determined based on the maximum value (median value) of the distribution of molecular weights at the end of the reaction. It can be calculated. For example, when analyzing the degree of deuteration of Compound A below, the molecular weight of the starting material below is 506, and the maximum molecular weight (median value) of Compound A below in the MS graph is 527, hydrogen at a position that can be substituted for the starting material below Since 21 of (26) were substituted with deuterium, it can be calculated that about 81% of hydrogen was deuterated.

In this specification, D means deuterium.

In this specification, “or” refers to an inclusive “or” and does not refer to an exclusive “or.” For example, condition A or B is satisfied by either: A is true (or exists) and B is false (or does not exist), A is false (or does not exist) and B is true (or exists), both A and B are true (or exist).

As used herein, “mixture thereof” or “mixture” means that two or more substances are included. The “mixture” or “mixture” may include a uniformly and/or non-uniformly mixed state, a dissolved state, a uniformly and/or non-uniformly dispersed state, etc., but is not limited thereto.

In this specification, “energy level” or “energy level” means energy magnitude. Therefore, the energy level is interpreted to mean the absolute value of the corresponding energy value. For example, a low or deep energy level means that the absolute value increases in the minus direction from the vacuum level.

Additionally, the organic light emitting device according to the present invention includes a first electrode; a second electrode provided opposite the first electrode; And an organic light-emitting device comprising at least one organic material layer provided between the first electrode and the second electrode, wherein at least one layer of the organic material layer contains the above-described compound.

The organic light emitting device of the present invention can be manufactured using conventional organic light emitting device manufacturing methods and materials, except that one or more organic material layers are formed using the above-described compounds.

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

The organic material layer of the organic light emitting device of the present invention may have a single-layer structure, or may have a multi-layer structure in which two or more organic material layers are stacked. For example, the organic light-emitting device of the present invention may have a structure including a hole injection layer, a hole transport layer, a layer that simultaneously performs hole injection and hole transport, a light-emitting layer, an electron transport layer, an electron injection layer, etc. as an organic material layer. However, the structure of the organic light emitting device is not limited to this and may include fewer or more organic material layers.

In the organic light emitting device of the present invention, the organic material layer may include one or more of an electron transport layer, an electron injection layer, and an electron injection and transport layer, and one or more of the layers includes the compound represented by Formula 1 can do.

In another organic light emitting device, the organic material layer may include an electron transport layer or an electron injection layer, and the electron transport layer or the electron injection layer may include the compound represented by Formula 1.

In the organic light emitting device of the present invention, the electron injection and transport layer includes the compound of Formula 1 and a metal complex.

In the organic light emitting device of the present invention, the organic material layer may include one or more layers among a hole injection layer, a hole transport layer, and a layer that performs both hole injection and hole transport, and one or more of the layers is represented by the formula (1) It may contain compounds.

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

In one embodiment of the present invention, the organic material layer includes a light-emitting layer, and the light-emitting layer includes the compound represented by Formula 1.

In one embodiment of the present invention, the light emitting layer includes a host and a dopant.

In one embodiment of the present invention, the light emitting layer may include one or more types of hosts.

In one embodiment of the present invention, the light emitting layer may include one or more types of dopants.

In one embodiment of the present invention, the light-emitting layer includes the compound represented by Formula 1 as a host.

In one embodiment of the present invention, the light-emitting layer includes the compound represented by Formula 1 as a host and an organic compound as a dopant.

In one embodiment of the present invention, the light-emitting layer includes the compound represented by Formula 1 as a host and a boron-based organic compound as a dopant.

In one embodiment of the present invention, the light-emitting layer includes the compound represented by Formula 1 as a host and an organic compound as a dopant.

In one embodiment of the present invention, the light emitting layer includes a host and a dopant at a weight ratio of 99:1 to 1:99.

In one embodiment of the present invention, the light-emitting layer includes a host and a dopant at a weight ratio of 99:1 to 50:50.

In one embodiment of the present invention, the light-emitting layer includes a host and a dopant at a weight ratio of 99:1 to 70:30.

In one embodiment of the present invention, the light-emitting layer includes a host and a dopant at a weight ratio of 99:1 to 80:20.

In one embodiment of the present invention, the light-emitting layer includes a host and a dopant at a weight ratio of 99:1 to 85:15.

In one 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.

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

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

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

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

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

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

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

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

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

(10) Anode/hole transport layer/electron suppression layer/light emitting layer/electron transport layer/cathode

(11) Anode/hole transport layer/electron suppression layer/light emitting layer/electron transport layer/electron injection layer/cathode

(12) Anode/hole injection layer/hole transport layer/electron suppression layer/light emitting layer/electron transport layer/cathode

(13) Anode/hole injection layer/hole transport layer/electron suppression layer/light-emitting layer/electron transport layer/electron injection layer/cathode

(14) Anode/hole transport layer/light emitting layer/hole suppression layer/electron transport layer/cathode

(15) Anode/hole transport layer/light emitting layer/hole suppression layer/electron transport layer/electron injection layer/cathode

(16) Anode/hole injection layer/hole transport layer/light emitting layer/hole suppression layer/electron transport layer/cathode

(17) Anode/hole injection layer/hole transport layer/light-emitting layer/hole suppression layer/electron transport layer/electron injection layer/cathode

(18) Anode/hole injection layer/hole transport layer/electron suppression layer/light emitting layer/hole blocking layer/electron injection and transport layer/cathode

The structure of the organic light emitting device of the present invention may have the same structure as shown in FIG. 1, but is not limited thereto.

Figure 1 illustrates the structure of an organic light-emitting device in which an anode 2, an organic material layer 3, and a cathode 4 are sequentially stacked on a substrate 1. In this structure, the compound represented by Formula 1 may be included in the organic layer 3.

2 shows an anode (2), a hole injection layer (5), a hole transport layer (6), a hole control layer (7), a light emitting layer (8), an electron control layer (9), and an electron transport layer (10) on the substrate (1). , the structure of an organic light emitting device in which the electron injection layer 11, the cathode 4, and the capping layer 12 are sequentially stacked is illustrated. In this structure, the compound represented by Formula 1 may be included in the light-emitting layer 8.

For example, the organic light emitting device according to the present invention deposits a metal, a conductive metal oxide, or an alloy thereof on a substrate using a physical vapor deposition (PVD) method such as sputtering or e-beam evaporation. An anode is formed by depositing a layer on top of a hole injection layer, a hole transport layer, a layer that performs both hole transport and hole injection, a light emitting layer, an electron transport layer, an electron injection layer, and a group consisting of a layer that performs both electron transport and electron injection. It can be manufactured by forming an organic material layer containing one or more selected layers and then depositing a material that can be used as a cathode thereon. In addition to this method, an organic light-emitting device can also be made by sequentially depositing a cathode material, an organic material layer, and an anode material on a substrate.

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

The anode is an electrode that injects holes, and the anode material is generally preferably a material with a large work function to facilitate hole injection into the organic layer. Specific examples of anode materials that can be used in the present invention include metals such as vanadium, chromium, copper, zinc, and gold, or alloys thereof; Metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO); Combination of metal and oxide such as ZnO:Al or SnO ₂ :Sb; Conductive polymers such as poly(3-methylthiophene), poly[3,4-(ethylene-1,2-dioxy)thiophene] (PEDOT), polypyrrole, and polyaniline are included, but are not limited to these.

The cathode is an electrode that injects electrons, and the cathode material is preferably a material with a low work function to facilitate electron injection into the organic layer. Specific examples of cathode materials include metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin and lead, or alloys thereof; There are, but are not limited to, multi-layered materials such as LiF/Al or LiO ₂ /Al.

The hole injection layer is a layer that serves to facilitate the injection of holes from the anode to the light emitting layer, and the hole injection material is a material that can well inject holes from the anode at a low voltage. HOMO (highest occupied) of the hole injection material It is preferable that the molecular orbital is between the work function of the anode material and the HOMO of the surrounding organic layer. Specific examples of hole injection materials include metal porphyrine, oligothiophene, arylamine-based organic material, hexanitrilehexaazatriphenylene-based organic material, quinacridone-based organic material, and perylene-based organic material. organic substances, anthraquinone, polyaniline, and polythiophene series conductive polymers, etc., but are not limited to these. The thickness of the hole injection layer may be 1 to 150 nm. If the thickness of the hole injection layer is 1 nm or more, there is an advantage in preventing the hole injection characteristics from deteriorating, and if it is 150 nm or less, the thickness of the hole injection layer is so thick that the driving voltage is increased to improve the movement of holes. There is an advantage to preventing this.

According to an exemplary embodiment of the present specification, the hole injection layer includes, but is not limited to, a compound represented by the following formula HI-1.

[Formula HI-1]

In the formula HI-1,

At least one of X'1 to X'6 is N, and the remainder is CH,

R309 to R314 are the same or different from each other, and are each independently hydrogen; heavy hydrogen; Nitrile group; Substituted or unsubstituted alkyl group; Substituted or unsubstituted amine group; Substituted or unsubstituted aryl group; Or it is a substituted or unsubstituted heteroaryl group, or it combines with adjacent groups to form a substituted or unsubstituted ring.

According to an exemplary embodiment of the present specification, X'1 to X'6 are N.

According to an exemplary embodiment of the present specification, R309 to R314 are nitrile groups.

According to an exemplary embodiment of the present specification, the formula HI-1 is represented by the following compound.

The hole transport layer may play a role in facilitating the transport of holes. The hole transport material is a material that can transport holes from the anode or hole injection layer and transfer them to the light emitting layer, and a material with high mobility for holes is suitable. Specific examples include arylamine-based organic materials, conductive polymers, and block copolymers with both conjugated and non-conjugated portions, but are not limited to these.

According to an exemplary embodiment of the present specification, the hole transport layer includes a compound represented by the following chemical formula HT-2, but is not limited thereto.

[Formula HT-1]

In the formula HT-1,

R400 to R403 are the same or different from each other, and are each independently hydrogen; heavy hydrogen; Substituted or unsubstituted alkyl group; Substituted or unsubstituted aryl group; Substituted or unsubstituted amine group; Substituted or unsubstituted heteroaryl group; and any one selected from the group consisting of combinations thereof, or by combining with adjacent groups to form a substituted or unsubstituted ring,

L402 is a substituted or unsubstituted arylene group, or a substituted or unsubstituted heteroarylene group.

According to an exemplary embodiment of the present specification, R400 to R403 are the same as or different from each other, and each independently represents a substituted or unsubstituted aryl group; Substituted or unsubstituted amine group; Substituted or unsubstituted heteroaryl group; and any one selected from the group consisting of combinations thereof.

According to an exemplary embodiment of the present specification, R402 is a phenyl group substituted with a carbazole group or an arylamine group; Biphenyl group substituted with carbazole group or arylamine group; and any one selected from the group consisting of combinations thereof.

According to an exemplary embodiment of the present specification, R400 and R401 are the same or different from each other and are each independently a substituted or unsubstituted aryl group, or are combined with adjacent groups to form an aromatic hydrocarbon ring substituted with an alkyl group.

According to an exemplary embodiment of the present specification, R400 and R401 are the same or different from each other, and are each independently a phenyl group, or are combined with adjacent groups to form a benzene ring.

According to an exemplary embodiment of the present specification, the formula HT-1 is selected from the following compounds.

A hole control layer may be provided between the hole transport layer and the light emitting layer. The hole control layer may be an amine compound or a material known in the art.

According to an exemplary embodiment of the present specification, the hole control layer includes a compound represented by the following formula HT-2, but is not limited thereto.

[Formula HT-2]

In the formula HT-2,

R403 to R405 are the same or different from each other, and are each independently hydrogen; heavy hydrogen; Substituted or unsubstituted alkyl group; Substituted or unsubstituted aryl group; Substituted or unsubstituted amine group; Substituted or unsubstituted heteroaryl group; and any one selected from the group consisting of combinations thereof, or by combining with adjacent groups to form a substituted or unsubstituted ring,

L403 is a substituted or unsubstituted arylene group, or a substituted or unsubstituted heteroarylene group.

According to an exemplary embodiment of the present specification, R403 to R405 are the same as or different from each other, and each independently represents a substituted or unsubstituted aryl group; Substituted or unsubstituted amine group; Substituted or unsubstituted heteroaryl group; and any one selected from the group consisting of combinations thereof.

According to an exemplary embodiment of the present specification, R405 is a phenyl group substituted with a carbazole group or an arylamine group; Biphenyl group substituted with carbazole group or arylamine group; and any one selected from the group consisting of combinations thereof.

According to an exemplary embodiment of the present specification, R403 and R404 are the same or different from each other and are each independently a substituted or unsubstituted aryl group, or are combined with adjacent groups to form an aromatic hydrocarbon ring substituted with an alkyl group.

According to an exemplary embodiment of the present specification, R403 and R404 are the same or different from each other, and are each independently a phenyl group, or are combined with adjacent groups to form a benzene ring.

According to an exemplary embodiment of the present specification, the formula HT-2 is selected from the following compounds.

An electron blocking layer may be provided between the hole transport layer and the light emitting layer. The electron suppressing layer may be made of the spiro compound described above or a material known in the art.

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 range by receiving and combining holes and electrons from the hole transport layer and the electron transport layer, respectively, and is preferably a material with good quantum efficiency for fluorescence or phosphorescence. Specific examples include 8-hydroxy-quinoline aluminum complex (Alq ₃ ); Carbazole-based compounds; dimerized styryl compounds; BAlq; 10-hydroxybenzoquinoline-metal compound; Compounds of the benzoxazole, benzthiazole and benzimidazole series; Poly(p-phenylenevinylene) (PPV) series polymer; Spiro compounds; Polyfluorene group, rubrene, etc., but are not limited to these.

Host materials for the light emitting layer include condensed aromatic ring derivatives or heterocyclic ring-containing compounds. Specifically, condensed aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, and fluoranthene compounds, and heterocycle-containing compounds include carbazole derivatives, dibenzofuran derivatives, and ladder-type compounds. These include, but are not limited to, furan compounds and pyrimidine derivatives.

When the light-emitting layer emits red light, the light-emitting dopants include PIQIr(acac)(bis(1-phenylsoquinoline)acetylacetonateiridium), PQIr(acac)(bis(1-phenylquinoline)acetylacetonate iridium), and PQIr(tris(1-phenylquinoline)iridium). ), phosphorescent materials such as PtOEP (octaethylporphyrin platinum), or fluorescent materials such as Alq ₃ (tris(8-hydroxyquinolino)aluminum) may be used, but are not limited to these. If the light-emitting layer emits green light, a phosphor such as Ir(ppy) ₃ (fac tris(2-phenylpyridine)iridium) or a fluorescent material such as Alq3 (tris(8-hydroxyquinolino)aluminum) can be used as the light-emitting dopant. However, it is not limited to this. If the light-emitting layer emits blue light, the light-emitting dopant may be a phosphorescent material such as (4,6-F2ppy) ₂ Irpic, spiro-DPVBi, spiro-6P, distylbenzene (DSB), distrylarylene (DSA), Fluorescent materials such as PFO-based polymers and PPV-based polymers may be used, but are not limited to these.

According to an exemplary embodiment of the present specification, the dopant is represented by a compound of the following formula D-2.

[Formula D-2]

In Formula D-2,

T1 to T5 are the same or different from each other, and are each independently hydrogen; Substituted or unsubstituted alkyl group; Substituted or unsubstituted amine group; Or a substituted or unsubstituted aryl group,

t3 and t4 are each integers from 1 to 4,

t5 is an integer from 1 to 3,

When t3 is 2 or more, the 2 or more T3 are the same or different from each other,

When t4 is 2 or more, the 2 or more T4 are the same or different from each other,

When t5 is 2 or more, the 2 or more T5s are the same or different from each other.

According to an exemplary embodiment of the present specification, T1 to T5 are the same or different from each other, and are each independently hydrogen; A substituted or unsubstituted straight-chain or branched alkyl group having 1 to 30 carbon atoms; A substituted or unsubstituted monocyclic or polycyclic arylamine group having 6 to 30 carbon atoms; Or it is a substituted or unsubstituted monocyclic or polycyclic aryl group having 6 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, T1 to T5 are the same or different from each other, and are each independently hydrogen; A straight or branched alkyl group having 1 to 30 carbon atoms; A monocyclic or polycyclic arylamine group having 6 to 30 carbon atoms; Or, it is a monocyclic or polycyclic aryl group having 6 to 30 carbon atoms that is substituted or unsubstituted with a straight-chain or branched alkyl group having 1 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, T1 to T5 are the same or different from each other, and are each independently hydrogen; methyl group; tert-butyl group; Diphenylamine group; Or it is a phenyl group substituted or unsubstituted with a methyl group, or a tert-butyl group.

According to an exemplary embodiment of the present specification, Formula D-2 is represented by the following compound.

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

An electron control layer may be provided between the electron transport layer and the light emitting layer, and materials known in the art may be used.

According to an exemplary embodiment of the present specification, the electron control layer includes a compound of the following formula E-1.

[Formula E-1]

In Formula E-1,

At least one of Z1 to Z3 is N, the others are CH,

L601 is directly bonded; Substituted or unsubstituted arylene group; Or a substituted or unsubstituted heteroarylene group,

Ar601 to Ar603 are the same or different from each other, and are each independently a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heteroaryl group.

According to an exemplary embodiment of the present specification, L601 is a substituted or unsubstituted monocyclic or polycyclic arylene group having 6 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, L601 is a phenylene group; Biphenylylene group; Or it is a naphthylene group.

According to an exemplary embodiment of the present specification, Ar601 to Ar603 are the same as or different from each other, and are each independently a substituted or unsubstituted monocyclic or polycyclic aryl group having 6 to 30 carbon atoms, or a heteroaryl group having 3 to 30 carbon atoms. .

According to an exemplary embodiment of the present specification, Ar601 to Ar603 are phenyl groups or spirofluorene xanthene groups.

According to an exemplary embodiment of the present specification, Formula E-1 is represented by the following compound.

The electron transport layer may play a role in facilitating the transport of electrons. The electron transport material is a material that can easily inject electrons from the cathode and transfer them to the light-emitting layer, and a material with high mobility for electrons is suitable. Specific examples include Al complex of 8-hydroxyquinoline; Complex containing Alq ₃ ; organic radical compounds; Hydroxyflavone-metal complexes, etc., but are not limited to these. The thickness of the electron transport layer may be 1 to 50 nm. If the thickness of the electron transport layer is 1 nm or more, there is an advantage in preventing the electron transport characteristics from deteriorating, and if it is 50 nm or less, the thickness of the electron transport layer is too thick to prevent the driving voltage from increasing to improve the movement of electrons. There are benefits to this.

According to an exemplary embodiment of the present specification, the electron control layer includes a compound of the following formula E-2.

[Formula E-2]

In the above formula E-2,

At least one of Z11 to Z13 is N, the others are CH,

L611 is directly bonded; Substituted or unsubstituted arylene group; Or a substituted or unsubstituted heteroarylene group,

Ar611 to Ar613 are the same or different from each other, and are each independently a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heteroaryl group.

According to an exemplary embodiment of the present specification, L611 is a substituted or unsubstituted monocyclic or polycyclic arylene group having 6 to 30 carbon atoms.

According to an exemplary embodiment of the present specification, L611 is a phenylene group; Biphenylylene group; Or it is a naphthylene group.

According to an exemplary embodiment of the present specification, Ar611 to Ar613 are the same or different from each other, and each independently represents a substituted or unsubstituted monocyclic or polycyclic aryl group having 6 to 30 carbon atoms, or a substituted or unsubstituted aryl group having 3 to 30 carbon atoms. It is a heteroaryl group.

According to an exemplary embodiment of the present specification, Ar611 to Ar613 are phenyl groups or spirofluorenexanthene groups.

According to an exemplary embodiment of the present specification, Formula E-2 is represented by the following compound.

The electron injection layer may serve to facilitate injection of electrons. The electron injection material has the ability to transport electrons, has an excellent electron injection effect from the cathode, a light emitting layer or a light emitting material, prevents movement of excitons generated in the light emitting layer to the hole injection layer, and also has an excellent electron injection effect from the cathode to the light emitting layer or light emitting material. , Compounds with excellent thin film forming ability are preferred. Specifically, fluorenone, anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, preorenylidene methane, anthrone, etc. and their derivatives, metals. These include, but are not limited to, complex compounds and nitrogen-containing five-membered ring derivatives.

Examples of the metal complex compounds 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-cresolato) gallium, bis(2-methyl-8-quinolinato)(1-naphtolato) aluminum, bis(2-methyl-8-quinolinato)(2-naphtolato) gallium, etc. It is not limited to this.

The hole blocking layer is a layer that prevents holes from reaching the cathode, and can generally be formed under the same conditions as the hole injection layer. Specifically, it includes oxadiazole derivatives, triazole derivatives, phenanthroline derivatives, BCP, aluminum complex, etc., but is not limited thereto.

The organic light emitting device according to the present invention may be a front emitting type, a back emitting type, or a double-sided emitting type depending on the material used.

The organic light emitting device of the present invention can be manufactured using conventional organic light emitting device manufacturing methods and materials, except that one or more organic material layers are formed using the above-described compounds.

The method for producing the compound of Formula 1 and the production of an organic light-emitting device using the same will be described in detail in the examples below. However, the following examples are for illustrating the present invention, and the scope of the present invention is not limited thereto.

In the following reaction formula, various types of intermediates can be synthesized by appropriately selecting starting materials known to those skilled in the art regarding the type and number of substituents. Reaction types and reaction conditions known in the art can be used.

Synthesis Example 1. Synthesis of compound BH-1

<1-a> Synthesis of compound BH-1-a

2-(tert-butyl)anthracene (50g, 213mmol), n-bromosuccinimide (12.7g, 71mmol), and FeCl ₃ (1.73g, 10.6mol) were dissolved in 850ml of chloroform and stirred under reflux. n-Bromosuccinimide (12.7g, 71mmol) was added twice at 30-minute intervals. React for 2 hours and then cool. 250 ml of 20% Na ₂ S ₂ O ₃ aqueous solution was added dropwise. The organic layer was separated using a separatory funnel and washed three times with distilled water. Residual moisture was removed with anhydrous magnesium sulfate. Chloroform was removed by distillation under reduced pressure. It was purified using column chromatography (eluent EA:Hexane=1:100). The obtained solid was recrystallized in EA to obtain 23 g of compound BH-1-a (yield 34%).

<1-b> Synthesis of compound BH-1-b

Compound BH-1-a (23 g, 73.4 mmol) and phenylboronic acid (8.84 g, 80.8 mmol) were dissolved in 1,4-dioxane (250 ml), and then Pd(PPh ₃ ) ₄ (4.2 g, 3.7 mmol) ) and 80 ml of 2M K ₂ CO ₃ aqueous solution were added and refluxed for 24 hours. The reaction solution was cooled, the water layer was removed, and 1,4-dioxane was removed by distillation under reduced pressure. After dissolving in chloroform, it was placed in a separatory funnel and washed three times with distilled water. The organic layer was dried with anhydrous magnesium sulfate. Chloroform was removed under reduced pressure and recrystallized with EA (ethyl acetate) to obtain compound BH-1-b (14 g, yield 61%).

<1-c> Synthesis of compound BH-1-c

The compound BH-1-b (14 g, 45.1 mmol) was dispersed in 180 ml of chloroform, and n-bromosuccinimide (8.0 g, 45.1 mmol) solution dissolved in 20 ml of dimethylformamide was slowly added dropwise. After reaction at room temperature for 2 hours, 90 ml of 20% Na ₂ S ₂ O ₃ aqueous solution was added dropwise. The organic layer was separated using a separatory funnel and washed three times with distilled water. Residual moisture was removed with anhydrous magnesium sulfate. Chloroform was removed by distillation under reduced pressure. Compound BH-1-c (12 g, yield 68%) was obtained by recrystallization from EA (ethyl acetate).

<1-d> Synthesis of compound BH-1

Compound BH-1-c (12 g, 30.8mmol) and naphtho[2,3-b]benzofuran-1-ylboronic acid (8.9g, 33.9mmol) were dissolved in 1,4-dioxane (120ml). , Pd(PPh ₃ ) ₄ (0.35 g, 0.31 mmol) and 30 ml of 2M K ₂ CO ₃ aqueous solution were added and refluxed for 24 hours. The reaction solution was cooled, and the resulting solid was filtered. After dissolving in chloroform, it was placed in a separatory funnel and washed three times with distilled water. The organic layer was dried with anhydrous magnesium sulfate. Chloroform was removed under reduced pressure and recrystallized with EA (ethyl acetate) to obtain compound BH-1 (9 g, yield 55%). [M+H ⁺ ]=527.3

Synthesis Example 2. Synthesis of compound BH-2

<2-a> Synthesis of compound BH-2-a

Compound BH-2-a was obtained in the same manner as in Synthesis Example 1-b, except that naphtho[2,3-b]benzofuran-1-ylboronic acid was used instead of phenylboronic acid.

<2-b> Synthesis of compound BH-2-b

Compound BH-2-b was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-2-a was used instead of compound BH-1-b.

<2-c> Synthesis of compound BH-2

In Synthesis Example 1-d, except that compound BH-2-b was used instead of compound BH-1-c, and naphthalene-1-ylboronic acid was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-2 was obtained by the same synthesis. [M+H ⁺ ]=577.3

Synthesis Example 3. Synthesis of compound BH-3

<3-a> Synthesis of compound BH-3-a

Compound BH-3-a was obtained in the same manner as in Synthesis Example 1-b, except that naphtho[2,3-b]benzofuran-2-ylboronic acid was used instead of phenylboronic acid.

<3-b> Synthesis of compound BH-3-b

Compound BH-3-b was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-3-a was used instead of compound BH-1-b.

<3-c> Synthesis of compound BH-3

In Synthesis Example 1-d, compound BH-3-b was used instead of compound BH-1-c, and [1,1'-biphenyl]-2- was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-3 was obtained by the same synthesis except that monoboronic acid was used. [M+H ⁺ ]=603.3

Synthesis Example 4. Synthesis of compound BH-4

<4-a> Synthesis of compound BH-4-a

Compound BH-4-a was obtained in the same manner as in Synthesis Example 1-b, except that [1,1'-biphenyl]-3-ylboronic acid was used instead of phenylboronic acid.

<4-b> Synthesis of compound BH-4-b

Compound BH-4-b was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-4-a was used instead of compound BH-1-b.

<4-c> Synthesis of compound BH-4

In Synthesis Example 1-d, compound BH-4-b was used instead of compound BH-1-c, and naphtho[1,2-b]benzofuran- was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-4 was obtained by the same synthesis except that 7-monoboronic acid was used. [M+H ⁺ ]=603.3

Synthesis Example 5. Synthesis of compound BH-5

<5-a> Synthesis of compound BH-5-a

Compound BH-5-a was obtained in the same manner as in Synthesis Example 1-a, except that 2-cyclohexylanthracene was used instead of 2-(tert-butyl)anthracene.

<5-b> Synthesis of compound BH-5-b

Compound BH-5-b was obtained by synthesizing in the same manner as in Synthesis Example 1-b, except that BH-5-a was used instead of compound BH-1-a and naphthalen-2-ylboronic acid was used instead of phenylboronic acid.

<5-c> Synthesis of compound BH-5-c

Compound BH-5-c was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-5-b was used instead of compound BH-1-b.

<5-d> Synthesis of compound BH-5

In Synthesis Example 1-d, compound BH-5-c was used instead of compound BH-1-c, and naphtho[2,3-b]benzofuran- was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-5 was obtained by the same synthesis except that 2-monoboronic acid was used. [M+H ⁺ ]=603.4

Synthesis Example 6. Synthesis of compound BH-6

<6-a> Synthesis of compound BH-6-a

Compound BH-6-a was obtained in the same manner as in Synthesis Example 1-b, except that (4-(naphthalen-2-yl)phenyl)boronic acid was used instead of phenylboronic acid.

<6-b> Synthesis of compound BH-6-b

Compound BH-6-b was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-6-a was used instead of compound BH-1-b.

<6-c> Synthesis of compound BH-6

Compound BH-6 was obtained by the same synthesis in Synthesis Example 1-d, except that compound BH-6-b was used instead of compound BH-1-c. [M+H ⁺ ]=653.3

Synthesis Example 7. Synthesis of compound BH-7

<7-a> Synthesis of compound BH-7-a

Compound BH-7-a was obtained in the same manner as in Synthesis Example 1-b, except that (2-(naphthalen-2-yl)phenyl)boronic acid was used instead of phenylboronic acid.

<7-b> Synthesis of compound BH-7-b

Compound BH-7-b was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-7-a was used instead of compound BH-1-b.

<7-c> Synthesis of compound BH-7

In Synthesis Example 1-d, compound BH-7-b was used instead of compound BH-1-c, and naphtho[1,2-b]benzofuran- was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-7 was obtained by the same synthesis except that 7-monoboronic acid was used. [M+H ⁺ ]=603.3

Synthesis Example 8. Synthesis of compound BH-8

<8-a> Synthesis of compound BH-8-a

Compound BH-8-a was obtained in the same manner as in Synthesis Example 1-b, except that naphtho[1,2-b]benzofuran-8-ylboronic acid was used instead of phenylboronic acid.

<8-b> Synthesis of compound BH-8-b

Compound BH-8-b was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-8-a was used instead of compound BH-1-b.

<8-c> Synthesis of compound BH-8

In Synthesis Example 1-d, compound BH-8-b was used instead of compound BH-1-c, and (5-phenylnaphthalen-2-yl)boronic acid was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-8 was obtained by the same synthesis except that . [M+H ⁺ ]=653.3

Synthesis Example 9. Synthesis of compound BH-9

<9-a> Synthesis of compound BH-9-a

Compound BH-9-a was obtained in the same manner as in Synthesis Example 1-b, except that naphtho[2,3-b]benzofuran-1-ylboronic acid was used instead of phenylboronic acid.

<9-b> Synthesis of compound BH-9-b

Compound BH-9-b was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-9-a was used instead of compound BH-1-b.

<9-c> Synthesis of compound BH-9

In Synthesis Example 1-d, compound BH-9-b was used instead of compound BH-1-c, and dibenzo[b,d]furan-2-ylbo was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-9 was obtained by the same synthesis except that ronic acid was used. [M+H ⁺ ]=617.2

Synthesis Example 10. Synthesis of compound BH-10

<10-a> Synthesis of compound BH-10-a

Compound BH-10-a was obtained in the same manner as in Synthesis Example 1-b, except that benzo[b]naphtho[2,3-d]thiophen-2-ylboronic acid was used instead of phenylboronic acid.

<10-b> Synthesis of compound BH-10-b

Compound BH-10-b was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-10-a was used instead of compound BH-1-b.

<10-c> Synthesis of compound BH-10

In Synthesis Example 1-d, except that compound BH-10-b was used instead of compound BH-1-c, and naphthalene-1-ylboronic acid was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-10 was obtained by the same synthesis. [M+H ⁺ ]=593.2

Synthesis Example 11. Synthesis of compound BH-11

<11-a> Synthesis of compound BH-11-a

Compound BH-11-a was obtained in the same manner as in Synthesis Example 1-a, except that 1-(anthracen-2-yl)adamantane was used instead of 2-(tert-butyl)anthracene.

<11-b> Synthesis of compound BH-11-b

Compound BH-11-b was obtained in the same manner as in Synthesis Example 1-b, except that BH-11-a was used instead of compound BH-1-a.

<11-c> Synthesis of compound BH-11-c

Compound BH-11-c was obtained through the same synthesis except that compound BH-11-b was used instead of compound BH-1-b in Synthesis Example 1-c.

<11-d> Synthesis of compound BH-11

In Synthesis Example 1-d, compound BH-11-c was used instead of compound BH-1-c, and 4,4,5,5-tetramethyl-2 was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-11 was obtained by the same synthesis except that -(10-phenylnaphtho[1,2-b]benzofuran-7-yl)-1,3,2-dioxaborolane was used. [M+H ⁺ ]=681.3

Synthesis Example 12. Synthesis of compound BH-12

<12-a> Synthesis of BH-12-a

100 g of 2-(tert-butyl)anthracene, 20 g of 5% Pt/C, 600 ml of toluene, and 1400 ml of D ₂ O were placed in a high pressure reactor and then charged with hydrogen. After raising the temperature to 180°C, the reaction was carried out for 24 hours. After completion of the reaction, the catalyst was filtered through a Celite pad and then extracted. After purification using an ethyl acetate:hexane = 1:100 column, 73 g of BH-12-a was obtained through EA (ethyl acetate) recrystallization. (yield 70%).

<12-b> Synthesis of compound BH-12-b

Compound BH-12-b was obtained in the same manner as in Synthesis Example 1-a, except that BH-12-a was used instead of 2-(tert-butyl)anthracene.

<12-c> Synthesis of compound BH-12-c

Compound BH-12-c was obtained by the same synthesis in Synthesis Example 1-b, except that BH-12-b was used instead of BH-1-a.

<12-d> Synthesis of compound BH-12-d

Compound BH-12-d was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-12-c was used instead of compound BH-1-b.

<12-e> Synthesis of compound BH-12

Compound BH-12 was obtained by the same synthesis in Synthesis Example 1-d, except that compound BH-12-d was used instead of compound BH-1-c. [M+H ⁺ ]=534.3

Synthesis Example 13. Synthesis of compound BH-13

<13-a> Synthesis of compound BH-13-a

In Synthesis Example 1-d, compound BH-9-b was used instead of compound BH-1-c, and [1,1'-biphenyl]-2- was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-13-a was obtained by the same synthesis except that monoboronic acid was used.

<13-b> Synthesis of compound BH-13

BH-13 was obtained by the same synthesis in Synthesis Example 12-a, except that compound BH-13-a was used instead of 2-(tert-butyl)anthracene. [M+H ⁺ ]=628.4

Synthesis Example 14. Synthesis of compound BH-14

<14-a> Synthesis of BH-14-a

BH-14-a was obtained by the same synthesis in Synthesis Example 12-a, except that 2-cyclohexylanthracene was used instead of 2-(tert-butyl)anthracene.

<14-b> Synthesis of compound BH-14-b

Compound BH-14-b was obtained in the same manner as in Synthesis Example 1-a, except that BH-14-a was used instead of 2-(tert-butyl)anthracene.

<14-c> Synthesis of compound BH-14-c

Compound BH was synthesized in the same manner as in Synthesis Example 1-b, except that BH-14-b was used instead of BH-1-a and naphtho[1,2-b]benzofuran-8-ylboronic acid was used instead of phenylboronic acid. -14-c was obtained.

<14-d> Synthesis of compound BH-14-d

Compound BH-14-d was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-14-c was used instead of compound BH-1-b.

<14-e> Synthesis of compound BH-14

In Synthesis Example 1-d, compound BH-14-d was used instead of compound BH-1-c, and [1,1':3',1'' was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-14 was obtained by the same synthesis except that -terphenyl]-5'-ylboronic acid was used. [M+H ⁺ ]=712.4

Synthesis Example 15. Synthesis of compound BH-15

<15-a> Synthesis of BH-15-a

100 g of 2-(tert-butyl)anthracene, 10 g of 10% Pd/C, 20 g of 5% Pt/C, 600 ml of toluene, and 1400 ml of D ₂ O were placed in a high pressure reactor and then charged with hydrogen. After raising the temperature to 180°C, the reaction was carried out for 24 hours. After completion of the reaction, the catalyst was filtered through a Celite pad and then extracted. After purification using an ethyl acetate:hexane = 1:100 column, 61 g of BH-15-a was obtained through EA (ethyl acetate) recrystallization. (yield 57%).

<15-b> Synthesis of compound BH-15-b

Compound BH-15-b was obtained in the same manner as in Synthesis Example 1-a, except that BH-15-a was used instead of 2-(tert-butyl)anthracene.

<15-c> Synthesis of compound BH-15-c

Compound BH was synthesized in the same manner as in Synthesis Example 1-b, except that BH-15-b was used instead of BH-1-a and naphtho[2,3-b]benzofuran-2-ylboronic acid was used instead of phenylboronic acid. -15-c was obtained.

<15-d> Synthesis of compound BH-15-d

Compound BH-15-d was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-15-c was used instead of compound BH-1-b.

<15-e> Synthesis of compound BH-15

In Synthesis Example 1-d, except that compound BH-15-d was used instead of compound BH-1-c, and naphthalene-1-ylboronic acid was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-15 was obtained by the same synthesis. [M+H ⁺ ]=593.4

Synthesis Example 16. Synthesis of compound BH-16

<16-a> Synthesis of compound BH-16-a

Compound BH-12-a (35 g, 109 mmol) and 2-(3-chloronaphtho[2,3-b]benzofuran-1-yl)4,4,5,5-tetramethyl-1,3 , 2-dioxaborolein (43.3g, 114mmol) was dissolved in tetrahydrofuran (350ml), then Pd(PPh ₃ ) ₄ (2.52g, 2.18 mmol) and 90ml of 2M K ₂ CO ₃ aqueous solution were added and incubated for 24 hours. It was refluxed. The reaction solution was cooled, the water layer was removed, and tetrahydrofuran was removed by distillation under reduced pressure. After dissolving in chloroform, it was placed in a separatory funnel and washed three times with distilled water. The organic layer was dried with anhydrous magnesium sulfate. Chloroform was removed under reduced pressure and recrystallized with EA (ethyl acetate) to obtain compound BH-16-a (30 g, yield 56%).

<16-b> Synthesis of compound BH-16-b

Compound BH-16-a (30 g, 60.8mmol) and (phenyl-d5)boronic acid (8.50g, 66.9mmol) were dissolved in 1,4-dioxane (300ml), then bis(tri-tert-butylphos) Fin) Palladium(0) (0.31g, 0.6 mmol) and 75ml of 2M K ₂ CO ₃ aqueous solution were added and refluxed for 24 hours. The reaction solution was cooled, the water layer was removed, and 1,4-dioxane was removed by distillation under reduced pressure. After dissolving in chloroform, it was placed in a separatory funnel and washed three times with distilled water. The organic layer was dried with anhydrous magnesium sulfate. Chloroform was removed under reduced pressure and recrystallized with EA (ethyl acetate) to obtain compound BH-16-b (24 g, yield 73%).

<16-c>Synthesis of compound BH-16-c

Compound BH-16-c was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-16-b was used instead of compound BH-1-b.

<16-d> Synthesis of compound BH-16

Synthesis was the same as in Synthesis Example 1-d, except that compound BH-16-c was used instead of compound BH-1-c, and phenylboronic acid was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Thus, compound BH-16 was obtained. [M+H ⁺ ]=615.3

Synthesis Example 17. Synthesis of compound BH-17

<17-a> Synthesis of BH-17-a

BH-17-a was obtained by the same synthesis in Synthesis Example 12-a, except that 1-(anthracen-2-yl)adamantane was used instead of 2-(tert-butyl)anthracene.

<17-b> Synthesis of compound BH-17-b

Compound BH-17-b was obtained in the same manner as in Synthesis Example 1-a, except that BH-17-a was used instead of 2-(tert-butyl)anthracene.

<17-c> Synthesis of compound BH-17-c

Compound BH was synthesized in the same manner as in Synthesis Example 1-b, except that BH-17-b was used instead of BH-1-a and naphtho[1,2-b]benzofuran-8-ylboronic acid was used instead of phenylboronic acid. -17-c was obtained.

<17-d> Synthesis of compound BH-17-d

Compound BH-17-d was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-17-c was used instead of compound BH-1-b.

<17-e> Synthesis of compound BH-17

In Synthesis Example 1-d, compound BH-17-d was used instead of compound BH-1-c, and [1,1'-biphenyl]-4- was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-17 was obtained by the same synthesis except that monoboronic acid was used. [M+H ⁺ ]=688.9

Synthesis Example 18. Synthesis of compound BH-18

<18-a> Synthesis of compound BH-18-a

Compound BH-18-a was synthesized in the same manner as in Synthesis Example 1-b, except that BH-12-b was used instead of BH-1-a and (naphthalen-1-yl-d7)boronic acid was used instead of phenylboronic acid. got it

<18-b> Synthesis of compound BH-18-b

Compound BH-18-b was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-18-a was used instead of compound BH-1-b.

<18-c> Synthesis of compound BH-18

In Synthesis Example 1-d, compound BH-18-b was used instead of compound BH-1-c, and naphtho[1,2-b]benzofuran- was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-18 was obtained by the same synthesis except that 7-monoboronic acid was used. [M+H ⁺ ]=591.3

Synthesis Example 19. Synthesis of compound BH-19

<19-a> Synthesis of compound BH-19-a

In Synthesis Example 16-a, compound BH-1-a was replaced with compound BH-12-a, 2-(3-chloronaphtho[2,3-b]benzofuran-1-yl)4,4,5,5 -Compound BH-19-a was synthesized in the same manner except that (4-chlorophenyl-2,3,5,6-d4)boronic acid was used instead of tetramethyl-1,3,2-dioxaborolein. got it

<19-b> Synthesis of compound BH-19-b

In Synthesis Example 16-b, except that compound BH-19-a was used instead of compound BH-16-a, and naphtho[2,3-b]benzofuran-2-ylboronic acid was used instead of (phenyl-d5)boronic acid. was synthesized in the same manner to obtain compound BH-19-b.

<19-c>Synthesis of compound BH-19-c

Compound BH-19-c was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-19-b was used instead of compound BH-1-b.

<19-d> Synthesis of compound BH-19

In Synthesis Example 1-d, except that compound BH-19-c was used instead of compound BH-1-c, and (phenyl-d5)boronic acid was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. was synthesized in the same manner to obtain compound BH-19. [M+H ⁺ ]=612.3

Synthesis Example 20. Synthesis of compound BH-20

<20-a> Synthesis of compound BH-20-a

Compound BH- was synthesized in the same manner as in Synthesis Example 1-b, except that BH-15-b was used instead of BH-1-a and (4-(naphthalen-1-yl)phenyl)boronic acid was used instead of phenylboronic acid. Got 20-a.

<20-b> Synthesis of compound BH-20-b

Compound BH-20-b was obtained by the same synthesis in Synthesis Example 1-c, except that compound BH-20-a was used instead of compound BH-1-b.

<20-c> Synthesis of compound BH-20

In Synthesis Example 1-d, compound BH-20-b was used instead of compound BH-1-c, and naphtho[2,3-b]benzofuran- was used instead of naphtho[2,3-b]benzofuran-1-ylboronic acid. Compound BH-20 was obtained by the same synthesis except that 2-monoboronic acid was used. [M+H ⁺ ]=669.4

By appropriately combining the production formulas described in the Examples of this specification and the intermediates based on common technical knowledge, all of the compounds of Formula 1 described in this specification can be prepared.

Example 1

A substrate on which ITO (indium tin oxide)/Ag/ITO was deposited at 70Å/1000Å/70Å as an anode was cut into 50mm x 50mm x 0.5mm, placed in distilled water with a dispersant dissolved in it, and washed ultrasonically. Detergent was used from Fischer Co., and distilled water was from Millipore Co. Secondary filtered distilled water was used as a product filter. After washing the ITO for 30 minutes, it was ultrasonic washed twice with distilled water for 10 minutes. After washing with distilled water, it was ultrasonic washed in the following solvent order: isopropyl alcohol, acetone, and methanol, and then dried.

HAT-CN was thermally vacuum deposited to a thickness of 50 Å on the anode to form a hole injection layer, and HTL1, a hole transport material, was vacuum deposited to a thickness of 1,150 Å on the anode to form a hole transport layer. Then, a hole control layer was formed using HTL2 (150Å). Subsequently, BH-1 as a host and BD-1 (weight ratio 95:5) as a dopant were simultaneously vacuum deposited to form a 20 nm thick light emitting layer. Then, 50Å of ETL2 was deposited to form an electron control layer, and the compound ETL1 and lithium quinolate (Liq) were mixed in a ratio of 7:3 to form an electron transport layer with a thickness of 250Å. Sequentially, magnesium and lithium fluoride (LiF) with a thickness of 50 Å were formed as an electron injection layer.

After forming the cathode with 200Å of magnesium and silver (1:4), 600Å of CP1 was deposited to complete the device. In the above process, the deposition rate of organic matter was maintained at 1Å/sec.

Examples 2 to 20 and Comparative Examples 1 to 6

An organic light-emitting device was manufactured in the same manner as in Example 1, except that the compounds listed in Table 1 below were used instead of BH-1 as the host of the light-emitting layer. At this time, the compound represented by Formula 1 of the present invention among the structures below was prepared through the same process as Synthesis Examples 1 to 20 described above.

In the organic light emitting devices manufactured in Examples 1 to 20 and Comparative Examples 1 to 6, the driving voltage and luminous efficiency were measured at a current density of 10 mA/cm ² , and the initial luminance was measured at a current density of 20 mA/cm ² The time to reach 95% of the comparison (LT) was measured, and the results are shown in the table below.

No. Host 10 mA/cm ² measured value L.T.
(T95%) V op Cd/A Example 1 BH-1 3.59 7.55 133 Example 2 BH-2 3.65 7.70 113 Example 3 BH-3 3.67 7.58 121 Example 4 BH-4 3.70 7.69 118 Example 5 BH-5 3.63 7.52 125 Example 6 BH-6 3.73 7.69 114 Example 7 BH-7 3.78 7.62 128 Example 8 BH-8 3.68 7.51 120 Example 9 BH-9 3.52 7.45 115 Example 10 BH-10 3.69 7.65 111 Example 11 BH-11 3.73 7.58 122 Example 12 BH-12 3.58 7.58 156 Example 13 BH-13 3.60 7.66 183 Example 14 BH-14 3.77 7.59 165 Example 15 BH-15 3.68 7.56 168 Example 16 BH-16 3.74 7.61 171 Example 17 BH-17 3.75 7.68 162 Example 18 BH-18 3.72 7.59 175 Example 19 BH-19 3.66 7.53 153 Example 20 BH-20 3.75 7.63 156 Comparative Example 1 BH-A 4.16 7.15 94 Comparative Example 2 BH-B 3.80 7.01 89 Comparative Example 3 BH-C 4.02 7.06 77 Comparative Example 4 BH-D 3.92 6.94 83 Comparative Example 5 BH-E 3.97 6.88 73 Comparative Example 6 BH-F 3.90 6.55 80

Examples 1 to 20 using the compound represented by Formula 1 of the present invention all exhibited characteristics of low voltage and high efficiency compared to Comparative Examples 1 to 6, and also showed superior lifespan compared to Comparative Examples 1 to 6. In particular, Examples 12 to 20 showed that lifespan was further improved by deuterium substitution. Although the preferred embodiment (host) of the present invention has been described above, the present invention is not limited thereto, and can be implemented with various modifications within the scope of the claims and the detailed description of the invention, which are also part of the invention. belongs to the category

1: substrate
2: anode
3: Organic layer
4: cathode
5: Hole injection layer
6: Hole transport layer
7: Hole control layer
8: Light-emitting layer
9: Electronic control layer
10: Electron transport layer
11: Electron injection layer

Claims (14)

Compound of formula 1:
[Formula 1]

In Formula 1,
R1, and R3 to R8 are the same or different from each other and are each independently hydrogen or deuterium,
R2 is a substituted or unsubstituted alkyl group, or a substituted or unsubstituted cycloalkyl group,
L1 and L2 are the same or different from each other and are each independently a direct bond, a substituted or unsubstituted arylene group, or a substituted or unsubstituted heteroarylene group,
At least one of A1 and A2 is of the following formula A-1 or A-2, and the remainder is a substituted or unsubstituted hydrocarbon ring group, or a substituted or unsubstituted 3- or 4-ring heteroaryl containing N, O, or S. It's awesome,
[Formula A-1]

[Formula A-2]

In the above formulas A-1 and A-2,
R9 and R10 are the same or different from each other, and are each independently hydrogen, deuterium, a halogen group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted group. It is a heteroaryl group,
R11 or R12 is a site that binds to L1 or L2,
R15 or R16 is a site that binds to L1 or L2,
A substituent among R11, R12, R15 and R16 that does not bind to L1 or L2; R13, R14, R17, and R18 are the same or different from each other, and are each independently hydrogen, deuterium, a halogen group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted aryl group, or It is a substituted or unsubstituted heteroaryl group,
X1 is O or S,
a and b are each integers from 1 to 6,
When a is 2 or more, R9 is the same or different from each other,
When b is 2 or more, R10 is the same or different from each other. The compound according to claim 1, wherein Formula 1 is the following Formula 1-1 or 1-2:
[Formula 1-1] [Formula 1-2]

In Formula 1-1 or 1-2, R1 to R9, R11 to R14, L1, L2, X1, A2 and a are as defined in Formula 1 and A-1. The compound according to claim 1, wherein the formula 1 is the following formula 1-3 or 1-4:
[Formula 1-3] [Formula 1-4]

In Formulas 1-3 and 1-4, R1 to R8, R10, R15 to R18, L1, L2, X1, A2, and b are as defined in Formulas 1 and A-2. The compound according to claim 1, wherein Formula 1 is Formula 2-1 or 2-2 below:
[Formula 2-1] [Formula 2-2]

In Formula 2-1 or 2-2, R1 to R9, R11 to R14, L1, L2, X1, A1 and a are as defined in Formula 1 and A-1. The compound according to claim 1, wherein Formula 1 is the following Formula 2-3 or 2-4:
[Formula 2-3] [Formula 2-4]

In Formulas 2-3 and 2-4, R1 to R8, R10, R15 to R18, L1, L2, X1, A1, and b are as defined in Formulas 1 and A-2. The compound according to claim 1, wherein R1, and R3 to R8 are deuterium. The compound according to claim 1, wherein A2 is an aryl group having 6 to 30 carbon atoms. The compound according to claim 1, wherein R2 is an alkyl group having 1 to 10 carbon atoms, or a cycloalkyl group having 3 to 20 carbon atoms. The compound according to claim 1, wherein L1 and L2 are the same or different from each other and are each independently a direct bond, an arylene group having 6 to 30 carbon atoms, or a heteroarylene group having 3 to 30 carbon atoms. The compound according to claim 1, wherein more than 15% of the substitutable positions in Formula 1 are substituted with deuterium. The method according to claim 1, wherein Formula 1 is any one of the following compounds:


first electrode; a second electrode provided opposite the first electrode; And an organic light-emitting device comprising at least one organic material layer provided between the first electrode and the second electrode, wherein at least one layer of the organic material layer includes the compound according to any one of claims 1 to 11. . The organic light-emitting device of claim 12, wherein the organic material layer includes a light-emitting layer, and the light-emitting layer includes the compound. The organic light-emitting device of claim 12, wherein the organic material layer includes a light-emitting layer, and the light-emitting layer includes the compound as a host.