KR102261231B1 - Copolymer and organic light emitting device comprising the same - Google Patents

Abstract

The present specification relates to a copolymer comprising a unit of Formula 1, and a unit of Formula 2; And it provides an organic light emitting device including the same.

Description

Copolymer, and an organic light emitting device comprising the same {COPOLYMER AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME}

The present specification relates to a copolymer, a coating composition comprising the copolymer, an organic light emitting device formed using the coating composition, and a method for manufacturing the same.

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

Conjugated polymers are widely used for polymer HTL materials among solvable OLED materials, which utilizes the difference in energy gap according to the length of the conjugation. In order to solve this problem, a method of breaking conjugation by limiting it to a specific length is used. Such polymers sandwiched between non-conjugated blocks are called conjugated-non-conjugated block copolymers (CNCP). The development of a polymer capable of controlling an energy gap by using a monomer including a silicon atom as a non-conjugated block is required.

US Patent Application Publication No. 2004-0251816

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

A copolymer comprising a unit of Formula 1 below, and a unit of Formula 2 below:

[Formula 1]

[Formula 2]

In Formulas 1 and 2,

은 다른 치환기, 단량체 또는 결합부에 결합되는 부위를 의미하고,

means a site bonded to another substituent, monomer or bonding portion,

R1 to R6 are hydrogen; heavy hydrogen; halogen group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group,

Ar1 to Ar5 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted arylene group; Or a substituted or unsubstituted heteroarylene group,

Ar6 and Ar7 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; a substituted or unsubstituted alkyl group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heteroaryl group,

a is an integer from 1 to 8,

b is 0 or 1,

When a is plural, structures in parentheses are the same or different from each other.

Another exemplary embodiment of the present specification provides a coating composition comprising the copolymer.

In addition, the first electrode; a second electrode provided to face the first electrode; and

One or more organic material layers are included between the first electrode and the second electrode,

At least one layer of the organic material layer provides an organic light emitting device comprising the coating composition or a cured product thereof.

Another exemplary embodiment of the present specification provides a method of manufacturing an organic light emitting device, wherein the step of forming the organic material layer formed by using the coating composition includes a drying step after applying the coating composition.

The hole injection layer/hole transport layer material using the copolymer of the present invention has high solubility in organic solvents and excellent hole transport properties in the device after film formation. In addition, it is not deformed by an additional solution process after the solution coating and heat treatment process, and efficiency and lifespan can be improved.

1 illustrates an organic light emitting diode according to an exemplary embodiment of the present specification.

Hereinafter, the present specification will be described in detail.

An exemplary embodiment of the present specification provides a copolymer comprising the unit of Formula 1 and the unit of Formula 2 above.

An exemplary embodiment of the present specification provides a coating composition comprising the copolymer or a cured product thereof.

An exemplary embodiment of the present specification includes a first electrode; a second electrode provided to face the first electrode; and at least one organic material layer between the first electrode and the second electrode, wherein at least one of the organic material layers provides an organic light emitting device including the coating composition or a cured product thereof.

An exemplary embodiment of the present specification provides a method for manufacturing an organic light emitting device, wherein the forming using the coating composition includes a drying step after applying the coating composition.

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

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

In the present specification, "combination" means connecting a plurality of structures or connecting different types of structures.

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

는 다른 치환기, 단량체 또는 결합부에 결합되는 부위를 의미한다.In this specification,

denotes a site bonded to other substituents, monomers, or binding groups.

In the present specification, the monomer may mean a repeating unit included in the polymer.

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

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

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

In the present specification, the halogen group may be fluorine, chlorine, bromine or iodine.

In the present specification, the number of carbon atoms of the carbonyl group is not particularly limited, but preferably from 1 to 30 carbon atoms.

In the present specification, in the ester group, the oxygen of the ester group may be substituted with a linear, branched or cyclic alkyl group having 1 to 25 carbon atoms or an aryl group having 6 to 30 carbon atoms.

In the present specification, the alkyl group may be linear or branched, and the number of carbon atoms is not particularly limited, but is preferably 1 to 30. Specific examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n-pentyl , isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl, n -Heptyl, 1-methylhexyl, cyclopentylmethyl, cyclohexylmethyl, octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhexyl, 2-propylpentyl, n-nonyl, 2,2-dimethyl heptyl, 1-ethyl-propyl, 1,1-dimethyl-propyl, isohexyl, 4-methylhexyl, 5-methylhexyl, and the like.

In the present specification, the cycloalkyl group is not particularly limited, but preferably has 3 to 30 carbon atoms, and specifically, cyclopropyl, cyclobutyl, cyclopentyl, 3-methylcyclopentyl, 2,3-dimethylcyclopentyl, cyclohexyl, 3-methylcyclohexyl, 4-methylcyclohexyl, 2,3-dimethylcyclohexyl, 3,4,5-trimethylcyclohexyl, 4-tert-butylcyclohexyl, cycloheptyl, cyclooctyl, etc., but are limited thereto it is not

In the present specification, the amine group is -NH ₂ ; an alkylamine group; N-arylalkylamine group; arylamine group; N-aryl heteroarylamine group; It may be selected from the group consisting of an N-alkylheteroarylamine group and a heteroarylamine group, and the number of carbon atoms is not particularly limited, but is preferably 1 to 30. Specific examples of the amine group include a methylamine group, a dimethylamine group, an ethylamine group, a diethylamine group, a phenylamine group, a naphthylamine group, a biphenylamine group, an anthracenylamine group, and a 9-methyl-anthracenylamine group. , diphenylamine group, N-phenylnaphthylamine group, ditolylamine group, N-phenyltolylamine group, triphenylamine group, and the like, but is not limited thereto.

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

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

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

In the present specification, the alkyl group in the alkylamine group, the N-arylalkylamine group, the alkylthioxy group, the alkylsulfoxy group, and the N-alkylheteroarylamine group is the same as the above-described alkyl group. Specifically, the alkyl thiooxy group includes a methyl thioxy group, ethyl thiooxy group, tert-butyl thioxy group, hexyl thioxy group, octyl thiooxy group, etc., and the alkyl sulfoxy group includes mesyl, ethyl sulfoxy group, propyl sulfoxy group, butyl sulfoxy group. and the like, but is not limited thereto.

In the present specification, the aryl group may be monocyclic or polycyclic.

When the aryl group is a monocyclic aryl group, the number of carbon atoms is not particularly limited, but preferably 6 to 30 carbon atoms. Specifically, the monocyclic aryl group may be a phenyl group, a biphenyl group, a terphenyl group, and the like, but is not limited thereto.

When the aryl group is a polycyclic aryl group, the number of carbon atoms is not particularly limited. It is preferable that it is C10-30. Specifically, the polycyclic aryl group may be a naphthyl group, an anthracenyl group, a phenanthryl group, a pyrenyl group, a perylenyl group, a chrysenyl group, a fluorenyl group, and the like, but is not limited thereto.

In the present specification, the fluorenyl group may be substituted, and adjacent substituents may combine with each other to form a ring.

,

,

및

등이 될 수 있다. 다만, 이에 한정되는 것은 아니다.When the fluorenyl group is substituted,

,

,

and

etc. can be However, the present invention is not limited thereto.

In the present specification, the aryl group in the aryloxy group, the arylthioxy group, the arylsulfoxy group, the N-arylalkylamine group, the N-arylheteroarylamine group and the arylphosphine group is the same as the above-described aryl group. Specifically, the aryloxy group includes a phenoxy group, p-tolyloxy group, m-tolyloxy group, 3,5-dimethyl-phenoxy group, 2,4,6-trimethylphenoxy group, p-tert-butylphenoxy group, 3- Biphenyloxy group, 4-biphenyloxy group, 1-naphthyloxy group, 2-naphthyloxy group, 4-methyl-1-naphthyloxy group, 5-methyl-2-naphthyloxy group, 1-anthryloxy group , 2-anthryloxy group, 9-anthryloxy group, 1-phenanthryloxy group, 3-phenanthryloxy group, 9-phenanthryloxy group, etc., and the arylthioxy group includes phenylthioxy group, 2- There is a methylphenylthioxy group, a 4-tert-butylphenylthioxy group, and the like, and the arylsulfoxy group includes a benzenesulfoxy group and a p-toluenesulfoxy group, but is not limited thereto.

In the present specification, examples of the arylamine group include a substituted or unsubstituted monoarylamine group, a substituted or unsubstituted diarylamine group, or a substituted or unsubstituted triarylamine group. The aryl group in the arylamine group may be a monocyclic aryl group or a polycyclic aryl group. The arylamine group including two or more aryl groups may include a monocyclic aryl group, a polycyclic aryl group, or a monocyclic aryl group and a polycyclic aryl group at the same time. For example, the aryl group in the arylamine group may be selected from the examples of the aryl group described above.

In the present specification, the heterocyclic group includes one or more atoms other than carbon and heteroatoms, and specifically, the heteroatoms may include one or more atoms selected from the group consisting of O, N, Se and S, and the like. The number of carbon atoms is not particularly limited, but preferably has 2 to 30 carbon atoms, and the heterocyclic group may be monocyclic or polycyclic. Examples of the heterocyclic group include a thiophene group, a furanyl group, a pyrrole group, an imidazolyl group, a thiazolyl group, an oxazolyl group, an oxadiazolyl group, a pyridyl group, a bipyridyl group, a pyrimidyl group, a triazinyl group, a triazinyl group Jolyl group, acridyl group, pyridazinyl group, pyrazinyl group, quinolinyl group, quinazolinyl group, quinoxalinyl group, phthalazinyl group, pyrido pyrimidyl group, pyrido pyrazinyl group, pyrazino pyrazinyl group , isoquinolinyl group, indolyl group, carbazolyl group, benzoxazolyl group, benzimidazolyl group, benzothiazolyl group, benzocarbazolyl group, benzothiophene group, dibenzothiophene group, benzofuranyl group, pe Nonthrolinyl group (phenanthroline), isoxazolyl group, thiadiazolyl group, phenothiazinyl group, dibenzofuranyl group, and the like, but is not limited thereto.

In the present specification, examples of the heteroarylamine group include a substituted or unsubstituted monoheteroarylamine group, a substituted or unsubstituted diheteroarylamine group, or a substituted or unsubstituted triheteroarylamine group. The heteroarylamine group including two or more heteroaryl groups may include a monocyclic heteroaryl group, a polycyclic heteroaryl group, or a monocyclic heteroaryl group and a polycyclic heteroaryl group at the same time. For example, the heteroaryl group in the heteroarylamine group may be selected from the examples of the heterocyclic group described above.

In the present specification, examples of the heteroaryl group in the N-arylheteroarylamine group and the N-alkylheteroarylamine group are the same as the examples of the heterocyclic group described above.

In the present specification, the copolymer further includes one or two or more of the units of the following formula (3) and the units of the following formula (4).

[Formula 3]

[Formula 4]

In Formulas 3 and 4,

R7 to R10 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted aryloxy group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted amine group; a substituted or unsubstituted silyl group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group, a thermosetting group or a photocurable group,

c is an integer from 0 to 6, and when c is plural, R9 is the same as or different from each other,

d is an integer from 0 to 4, and when d is plural, R10 is the same as or different from each other.

In the present specification, Chemical Formula 4 is selected from the following Chemical Formulas 5 to 7.

[Formula 5]

[Formula 6]

[Formula 7]

In Formulas 5 to 7, R10' has the same definition as R10.

In an exemplary embodiment of the present specification, R1 to R4 are the same as or different from each other, and each independently hydrogen; halogen group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group.

In an exemplary embodiment of the present specification, R1 to R4 are the same as or different from each other, and each independently represents a substituted or unsubstituted C1 to C20 alkyl group.

In an exemplary embodiment of the present specification, R1 to R4 are the same as or different from each other, and each independently a substituted or unsubstituted methyl group, a substituted or unsubstituted ethyl group, a substituted or unsubstituted propyl group, a substituted or unsubstituted isopropyl group, substituted or unsubstituted butyl group, substituted or unsubstituted n-butyl group, substituted or unsubstituted terbutyl group, substituted or unsubstituted pentyl group, substituted or unsubstituted hexyl group, substituted or unsubstituted a substituted heptyl group, a substituted or unsubstituted octyl group, a substituted or unsubstituted nonyl group, or a substituted or unsubstituted decyl group.

In an exemplary embodiment of the present specification, R1 to R4 are the same as or different from each other, and each independently represents a halogen group.

In an exemplary embodiment of the present specification, R1 to R4 are the same as or different from each other, and each independently represents F, Br, Cl, or I.

In an exemplary embodiment of the present specification, R1 to R4 are the same as or different from each other, and each independently represents a substituted or unsubstituted C6-C20 aryl group.

In an exemplary embodiment of the present specification, R1 to R4 are the same as or different from each other, and each independently represents a substituted or unsubstituted monocyclic aryl group having 6 to 20 carbon atoms.

In an exemplary embodiment of the present specification, R1 to R4 are the same as or different from each other, and each independently represents a substituted or unsubstituted polycyclic aryl group having 10 to 20 carbon atoms.

In an exemplary embodiment of the present specification, R1 to R4 are the same as or different from each other, and each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted a terphenyl group, a substituted or unsubstituted anthracene group, a substituted or unsubstituted phenanthrene group, a substituted or unsubstituted pyrene group, or a substituted or unsubstituted triphenylene group.

In an exemplary embodiment of the present specification, R1 to R4 are the same as or different from each other, and each independently represents a phenyl group, a biphenyl group, a naphthyl group, a terphenyl group, an anthracene group, a phenanthrene group, a pyrene group, or a triphenylene group.

In an exemplary embodiment of the present specification, R1 to R4 are the same as or different from each other, and each independently represents a methyl group, an ethyl group, a terbutyl group, F, or a phenyl group.

In an exemplary embodiment of the present specification, R5 and R6 are hydrogen.

In an exemplary embodiment of the present specification, R7 and R8 are the same as or different from each other, and each independently represent an alkyl group having 1 to 10 carbon atoms.

In an exemplary embodiment of the present specification, R7 and R8 are the same as or different from each other, and each independently represent a linear alkyl group having 1 to 10 carbon atoms, or a branched alkyl group having 1 to 10 carbon atoms.

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

In an exemplary embodiment of the present specification, R10 is a thermosetting group or a photocurable group.

According to an exemplary embodiment of the present specification, R10 is a thermosetting group or a photocurable group represented by any one of the following structural formulas.

In the structural formula,

Wherein Ri to Riv are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted aryloxy group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group,

Rv is O, a substituted or unsubstituted alkylene group, a substituted or unsubstituted alkoxyylene group, or a substituted or unsubstituted arylene group,

r is an integer from 0 to 4, and when r is plural, Riv is the same as or different from each other,

s is an integer from 0 to 5, and when s is plural, Riii are the same as or different from each other.

In an exemplary embodiment of the present specification, R10 is an alkoxy group unsubstituted or substituted with an aryl group unsubstituted or substituted with an alkenyl group.

In an exemplary embodiment of the present specification, R10 is an alkoxy group unsubstituted or substituted with a styrene group.

In the exemplary embodiment of the present specification, R10 is an alkoxy group having 1 to 10 carbon atoms that is unsubstituted or substituted with a styrene group.

In an exemplary embodiment of the present specification, R10 is a methoxy group unsubstituted or substituted with a styrene group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently is a direct bond; a substituted or unsubstituted arylene group; Or a substituted or unsubstituted heteroarylene group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently is a direct bond; a substituted or unsubstituted monocyclic arylene group; a substituted or unsubstituted polycyclic arylene group; Or a substituted or unsubstituted heteroarylene group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently is a direct bond; a substituted or unsubstituted monocyclic arylene group having 6 to 20 carbon atoms; a substituted or unsubstituted polycyclic arylene group having 3 to 20 carbon atoms; Or a substituted or unsubstituted heteroarylene group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently is a direct bond; a monocyclic arylene group unsubstituted or substituted with an alkyl group; or a polycyclic arylene group unsubstituted or substituted with an alkyl group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are the same as or different from each other, and each independently a substituted or unsubstituted phenylene group; a substituted or unsubstituted biphenylenylene group; a substituted or unsubstituted terphenyllenylene group; a substituted or unsubstituted anthracenylene group; a substituted or unsubstituted naphthylene group; a substituted or unsubstituted fluorenylene group; or a substituted or unsubstituted phenanthrenylene group.

In an exemplary embodiment of the present specification, Ar1 and Ar2 are a phenylene group; naphthylene group; biphenylenylene group; or a dimethyl fluorenylene group.

In an exemplary embodiment of the present specification, Ar3 to Ar5 are the same as or different from each other, and each independently a substituted or unsubstituted monocyclic arylene group; a substituted or unsubstituted polycyclic arylene group; Or a substituted or unsubstituted heteroarylene group.

In an exemplary embodiment of the present specification, Ar3 to Ar5 are the same as or different from each other, and each independently a substituted or unsubstituted monocyclic arylene group having 10 to 20 carbon atoms; a substituted or unsubstituted polycyclic arylene group having 10 to 20 carbon atoms; or a substituted or unsubstituted C 3 to C 20 heteroarylene group.

In an exemplary embodiment of the present specification, Ar3 to Ar5 are the same as or different from each other, and each independently a substituted or unsubstituted phenylene group; a substituted or unsubstituted biphenylenylene group; a substituted or unsubstituted terphenyllenylene group; a substituted or unsubstituted anthracenylene group; a substituted or unsubstituted naphthylene group; a substituted or unsubstituted fluorenylene group; or a substituted or unsubstituted phenanthrenylene group.

In an exemplary embodiment of the present specification, Ar3 to Ar5 are phenylene groups.

In an exemplary embodiment of the present specification, Ar6 and Ar7 are the same as or different from each other, and each independently hydrogen; a substituted or unsubstituted monocyclic aryl group; a substituted or unsubstituted polycyclic aryl group; Or a substituted or unsubstituted heteroaryl group.

In an exemplary embodiment of the present specification, Ar6 and Ar7 are the same as or different from each other, and each independently hydrogen; a substituted or unsubstituted monocyclic aryl group having 6 to 20 carbon atoms; a substituted or unsubstituted polycyclic aryl group having 10 to 20 carbon atoms; Or a substituted or unsubstituted heteroaryl group.

In an exemplary embodiment of the present specification, Ar6 and Ar7 are the same as or different from each other, and each independently represents an aryl group having 6 to 20 carbon atoms substituted with a heteroaryl group unsubstituted or substituted with an aryl group.

In an exemplary embodiment of the present specification, Ar6 and Ar7 are phenyl groups.

According to an exemplary embodiment of the present specification, the copolymer includes one or two or more units represented by the following Chemical Formulas 1-1 to 1-3.

[Formula 1-1]

[Formula 1-2]

[Formula 1-3]

In Formulas 1-1 to 1-3,

Ar1 to Ar7, R1 to R10, and a to d are as defined in Formulas 1 to 4 above.

According to an exemplary embodiment of the present specification, the copolymer includes Formula 1-3.

According to an exemplary embodiment of the present specification, the copolymer includes Chemical Formulas 1-1 and 1-3.

According to an exemplary embodiment of the present specification, the copolymer includes Chemical Formulas 1-1 to 1-3.

According to an exemplary embodiment of the present specification, the copolymer includes one or two or more units represented by the following Chemical Formulas 1-4 to 1-6.

[Formula 1-4]

[Formula 1-5]

[Formula 1-6]

In Formulas 1-4 to 1-6,

Ar1 to Ar7, R1 to R6, R10, a, b, and d are as defined in Formulas 1 to 4 above.

According to an exemplary embodiment of the present specification, the copolymer includes Formulas 1-4 to 1-6.

According to an exemplary embodiment of the present specification, the copolymer includes Formulas 1-4 and 1-6.

According to an exemplary embodiment of the present specification, the copolymer includes Formula 1-5.

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

According to an exemplary embodiment of the present specification, the copolymer has a number average molecular weight of 1,000 to 10,000,000 g/mol.

According to an exemplary embodiment of the present specification, the copolymer includes a structure of the following Chemical Formula 1-7.

[Formula 1-7]

In Formula 1-7

Ar1 to Ar7, R1 to R10, and a to d are as defined in Formulas 1 to 4 above.

Wherein o to q are the molar ratio of each unit,

When o+p+q=1,

o is a molar ratio of 0.025 to 0.95,

p is a molar ratio of 0.025 to 0.95,

q is a molar ratio of 0.025 to 0.95.

According to an exemplary embodiment of the present specification, the copolymer is a copolymer having any one of the following structures.

상기 구조식에 있어서,

In the structural formula,

o to q are the molar ratios of each unit, and when o+p+q=1,

o is a molar ratio of 0.025 to 0.95,

p is a molar ratio of 0.025 to 0.95,

q is a molar ratio of 0.025 to 0.95.

According to an exemplary embodiment of the present specification, o is a molar ratio of 0.5 to 0.9.

According to an exemplary embodiment of the present specification, p is a molar ratio of 0.1 to 0.5.

According to an exemplary embodiment of the present specification, q is a molar ratio of 0.1 to 0.5.

According to an exemplary embodiment of the present specification, the end of the copolymer may be hydrogen or an alkyl group.

According to an exemplary embodiment of the present specification, the coating composition includes the copolymer.

According to an exemplary embodiment of the present specification, the coating composition includes the copolymer in an amount of 0.1 to 30% by weight.

According to an exemplary embodiment of the present specification, the coating composition includes the copolymer in an amount of 1 to 10% by weight.

The organic light emitting device of the present specification may be manufactured by materials and methods known in the art, except that at least one layer of the organic material layer is formed using a coating composition including the copolymer.

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

1 illustrates a structure of an organic light emitting device in which a first electrode 2 , an organic material layer 3 , a light emitting layer 4 , and a second electrode 5 are sequentially stacked on a substrate 1 .

In an exemplary embodiment of the present invention, the organic light emitting device includes a first electrode; a second electrode provided to face the first electrode; and at least one organic material layer between the first electrode and the second electrode, wherein at least one organic material layer includes the coating composition or a cured product thereof.

In an exemplary embodiment of the present invention, the organic material layer includes a hole transport layer, a hole injection layer, or a layer that transports and injects holes at the same time, and the hole transport layer, the hole injection layer, or a layer that performs both hole transport and hole injection at the same time is and the coating composition or a cured product thereof.

In an exemplary embodiment of the present invention, the organic material layer includes an electron injection layer, an electron transport layer, or a layer that simultaneously injects and transports electrons, and the electron injection layer, the electron transport layer, or the layer that performs both injection and transport of electrons at the same time is and the coating composition or a cured product thereof.

For example, the organic light emitting diode according to the present invention uses a PVD (physical vapor deposition) method, such as sputtering or e-beam evaporation, to form a metal or a conductive metal oxide or an alloy thereof on a substrate. is deposited to form an anode, an organic material layer including a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, and an organic material layer including the copolymer are formed thereon, and then a material that can be used as a cathode is deposited thereon can be In addition to this method, an organic light emitting diode may be manufactured by sequentially depositing a cathode material, an organic material layer, and an anode material on a substrate.

As the anode material, a material having a large work function is generally preferable to facilitate hole injection into the organic material layer. Specific examples of the anode material that can be used in the present invention include metals such as vanadium, chromium, copper, zinc, gold, or alloys thereof; metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO); ZnO:Al or SnO ₂ : a combination of a metal such as Sb and an oxide; poly(3-methyl compound), poly[3,4-(ethylene-1,2-dioxy) compound] (PEDT), polypyrrole and conductive polymers such as polyaniline, and the like, but are not limited thereto.

The cathode material is preferably a material having a small work function to facilitate electron injection into the organic material layer. Specific examples of the negative electrode material include metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin and lead, or alloys thereof; and a multilayer structure material such as LiF/Al or LiO ₂ /Al, but is not limited thereto.

The hole injection material is a material capable of well injecting holes from the anode at a low voltage, and it is preferable that the highest occupied molecular orbital (HOMO) of the hole injection material is between the work function of the anode material and the HOMO of the surrounding organic material layer. Specific examples of the hole injection material include metal porphyrine, oligothiophene, arylamine-based organic material, hexanitrile hexaazatriphenylene-based organic material, quinacridone-based organic material, and perylene-based organic material. of organic substances, anthraquinones, and conductive polymers based on polyaniline and polycompounds, but is not limited thereto.

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

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

The emission layer may include a host material and a dopant material. The host material includes a condensed aromatic ring derivative or a compound containing a hetero ring. Specifically, condensed aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, fluoranthene compounds, etc., and heterocyclic-containing compounds include carbazole derivatives, dibenzofuran derivatives, ladder type Furan compounds, pyrimidine derivatives, and the like, but are not limited thereto.

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

The organic light emitting device of the present specification may be manufactured by materials and methods known in the art, except that at least one layer of the organic material layer is formed using a coating composition including the copolymer.

For example, the organic light emitting device of the present specification may be manufactured by sequentially stacking an anode, an organic material layer, and a cathode on a substrate. At this time, by using a PVD (physical vapor deposition) method such as sputtering or e-beam evaporation, a metal or conductive metal oxide or an alloy thereof is deposited on a substrate to form an anode. and forming an organic material layer including a hole injection layer, a hole transport layer, a light emitting layer and an electron transport layer thereon, and then depositing a material that can be used as a cathode thereon. In addition to this method, an organic light emitting diode may be manufactured by sequentially depositing a cathode material, an organic material layer, and an anode material on a substrate.

The present specification also provides a method of manufacturing an organic light emitting device formed using the coating composition.

Specifically, in one embodiment of the present specification, preparing a substrate; forming a cathode or an anode on the substrate; forming one or more organic material layers on the cathode or anode; and forming an anode or a cathode on the organic material layer, wherein at least one layer of the organic material layer is formed using the coating composition or a cured product thereof.

The step of forming one or more layers of the organic material layer using the coating composition may include a drying step after applying the coating composition. If necessary, the drying step may include a curing step. The form of the terminal vinyl group of the copolymer may be modified through the curing step.

In one embodiment of the present specification, the organic material layer formed using the coating composition is formed using a solution process.

In another embodiment, the organic material layer formed using the coating composition is formed by a printing method.

In the present specification, the printing method includes, for example, inkjet printing, nozzle printing, offset printing, transfer printing, or screen printing, but is not limited thereto.

Since the coating composition according to an exemplary embodiment of the present specification is suitable for a solution process due to its structural characteristics, it can be formed by a printing method, so that it is economically effective in terms of time and cost when manufacturing a device.

In an exemplary embodiment of the present specification, the step of forming the organic material layer formed using the coating composition includes heat treatment or vacuum drying. Residual solvent is removed through the heat treatment or vacuum drying step.

In one embodiment of the present specification, the heat treatment or vacuum drying may include a curing step.

In one embodiment of the present specification, as the polymer binder, one that does not extremely inhibit charge transport and does not have strong absorption for visible light is preferably used. Examples of the polymer binder include poly(N-vinylcarbazole), polyaniline and derivatives thereof, polythiophene and derivatives thereof, poly(p-phenylenevinylene) and derivatives thereof, poly(2,5-thienylenevinylene) and Derivatives thereof, polycarbonate, polyacrylate, polymethyl acrylate, polymethyl methacrylate, polystyrene, polyvinyl chloride, polysiloxane and the like are exemplified.

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

The electron transport material is a layer that receives electrons from the electron injection layer and transports them to the light emitting layer. The electron transport material is a material that can receive electrons well from the cathode and transfer them to the light emitting layer, and has high electron mobility. This is suitable. Specific examples include Al complex of 8-hydroxyquinoline; complexes containing Alq _{3 ;} organic radical compounds; hydroxyflavone-metal complexes, and the like, but are not limited thereto. The electron transport layer may be used with any desired cathode material as used in accordance with the prior art. In particular, examples of suitable cathode materials are conventional materials having a low work function and followed by a layer of aluminum or silver. Specifically cesium, barium, calcium, ytterbium and samarium, followed in each case by an aluminum layer or a silver layer.

The electron injection layer is a layer that injects electrons from the electrode, has the ability to transport electrons, has an electron injection effect from the cathode, an excellent electron injection effect with respect to the light emitting layer or the light emitting material, and hole injection of excitons generated in the light emitting layer A compound which prevents movement to a layer and is excellent in the ability to form a thin film is preferable. Specifically, fluorenone, anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, preorenylidene methane, anthrone, etc., derivatives thereof, metals complex compounds and nitrogen-containing 5-membered ring derivatives, but are not limited thereto.

Examples of the metal complex compound include 8-hydroxyquinolinato lithium, bis(8-hydroxyquinolinato)zinc, bis(8-hydroxyquinolinato)copper, bis(8-hydroxyquinolinato)manganese, Tris(8-hydroxyquinolinato)aluminum, tris(2-methyl-8-hydroxyquinolinato)aluminum, tris(8-hydroxyquinolinato)gallium, bis(10-hydroxybenzo[h] Quinolinato) beryllium, bis (10-hydroxybenzo [h] quinolinato) zinc, bis (2-methyl-8-quinolinato) chlorogallium, bis (2-methyl-8-quinolinato) ( o-crezolato)gallium, bis(2-methyl-8-quinolinato)(1-naphtolato)aluminum, bis(2-methyl-8-quinolinato)(2-naphtolato)gallium, etc. However, the present invention is not limited thereto.

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

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

The method for preparing the copolymer and the preparation of an organic light emitting device using them will be described in detail in the following Examples. However, the following examples are intended to illustrate the present invention, and the scope of the present invention is not limited thereto.

manufacturing example 1. Synthesis of Monomer 1

After dissolving 1,4-dibromobenzene (1,4-dibromobenzene) (4.71 g, 20.0 mmol) in tetrahydrofuran (anhydrous THF), the temperature was set to minus 78°C. N-butyllithium (n-butyllithium) (4.4 mL, 11.0 mmol) was added and stirred for 30 minutes. 1,2-bis(chlorodimethylsilyl)ethane (2.15 g, 10.0 mmol) was added, and the reaction was carried out by stirring at room temperature for 3 hours. The reaction was terminated with ammonium chloride (NH 4 Cl, ammonium chloride), the organic layer was extracted with ethyl acetate (EA _{), moisture was removed with magnesium sulfate (MgSO 4} ), dried, and column chromatography was performed. Monomer 1 was obtained by recrystallization under reduced pressure with acetone. The NMR data of monomer 1 is as follows.

1H NMR (500 MHz): δ = 7.47 (d, 4H), 7.41 (d, 4H), 0.58 (s, 4H), 0.22 (s, 12H)

manufacturing example 2. Synthesis of Monomer 2

After dissolving 1,4-dibromobenzene (1,4-dibromobenzene) (4.71 g, 20.0 mmol) in tetrahydrofuran (anhydrous THF), the temperature was set to minus 78°C. N-butyllithium (n-butyllithium) (4.4 mL, 11.0 mmol) was added and stirred for 30 minutes. 1,2-bis(chlorodiethylsilyl)butane (2.99 g, 10.0 mmol) was added, and the reaction was carried out by stirring at room temperature for 3 hours. The reaction was terminated with ammonium chloride (NH 4 Cl, ammonium chloride), the organic layer was extracted with ethyl acetate (EA _{), moisture was removed with magnesium sulfate (MgSO 4} ), dried, and column chromatography was performed. Monomer 2 was obtained by recrystallization under reduced pressure with acetone. The NMR data of monomer 2 is as follows.

1H NMR (500 MHz): δ = 7.48 (d, 4H), 7.42 (d, 4H), 1.24-1.22 (m, 4H), 0.94 (t, 12H), 0.62-0.58 (m, 8H)

manufacturing example 3. Synthesis of Monomer 3

After 2,6-dibromonaphthalene (2,6-dibromonaphthalene) (5.72 g, 20.0 mmol) was dissolved in tetrahydrofuran (anhydrous THF), the temperature was set to minus 78°C. N-butyllithium (n-butyllithium) (4.4 mL, 11.0 mmol) was added and stirred for 30 minutes. 1,2-bis(chlorodimethylsilyl)methane (1,2-bis(chlorodimethylsilyl)methane) (2.01 g, 10.0 mmol) was added, and the reaction was carried out by stirring at room temperature for 3 hours. The reaction was terminated with ammonium chloride (NH ₄ Cl, ammonium chloride), the organic layer was extracted with ethyl acetate (EA _{), moisture was removed with magnesium sulfate (MgSO 4} ), dried, and column chromatography was performed. Monomer 3 was obtained by recrystallization under reduced pressure with acetone. The NMR data of monomer 3 is as follows.

1H NMR (500 MHz): δ = 8.13 (s, 2H), 8.04-7.94 (m, 6H), 7.71 (s, 2H), 7.51 (s, 2H), 0.59 (s, 2H), 0.23 (s, 12H)

manufacturing example 4. Synthesis of Monomer 4

2,7-dibromo-9,9-dimethyl-9H-fluorene (7.04 g, 20.0 mmol) was mixed with tetrahydrofuran (anhydrous THF) After dissolving in , the temperature was set to -78 °C. N-butyllithium (n-butyllithium) (4.4 mL, 11.0 mmol) was added and stirred for 30 minutes. 1,2-bis(chlorodimethylsilyl)ethane (2.15 g, 10.0 mmol) was added, and the reaction was carried out by stirring at room temperature for 3 hours. The reaction was terminated with ammonium chloride (NH ₄ Cl, ammonium chloride), the organic layer was extracted with ethyl acetate (EA _{), moisture was removed with magnesium sulfate (MgSO 4} ), dried, and column chromatography was performed. Monomer 1 was obtained by recrystallization under reduced pressure with acetone.

manufacturing example 5. Synthesis of Copolymer 1

Monomer 5 (2,2 '- (9,9- dioctyl-9 H -fluorene-2,7-diyl) bis (4,4,5,5-tetramethyl-1,3,2-dioxaborolane)) (1 g , 1.56 mmol), Monomer 6 4-bromo- N- (4-bromophenyl) -N -phenylaniline (439.4 mg, 1.09 mmol), Monomer 7 4,4'-(2,5-dibromo-1,4-phenylene) bis(oxy)bis(methylene)bis(vinylbenzene) (109.5 mg. 0.24 mmol) and monomer 1 (0.24 mmol) were dissolved in toluene. The temperature was raised to 90 ℃ _{, tetraethylammonium hydroxide (Et 4} NOH, tetraethylammonium hydroxide) (20wt% aqueous, 5 mL) was added and stirred for 30 minutes. Thereafter, Pd(PPh ₃ ) ₄ (90.1 mg, 0.078 mmol) dissolved in toluene was added to carry out a Suzuki reaction. After the reaction was terminated by endcapping, the solid produced by precipitation in methanol was filtered to obtain copolymer 1 . As a result of the preparation, a polymer having a weight average molecular weight of 30 to 40 kg/mol was prepared.

manufacturing example 6. Synthesis of copolymer 2

Monomer 5 (2,2 '- (9,9- dioctyl-9 H -fluorene-2,7-diyl) bis (4,4,5,5-tetramethyl-1,3,2-dioxaborolane)) (1 g , 1.56 mmol), Monomer 6 4-bromo- N- (4-bromophenyl) -N -phenylaniline (439.4 mg, 1.09 mmol), Monomer 7 4,4'-(2,5-dibromo-1,4-phenylene) bis(oxy)bis(methylene)bis(vinylbenzene) (109.5 mg. 0.24 mmol) and monomer 3 (0.24 mmol) were dissolved in toluene. The temperature was raised to 90 ℃ _{, tetraethylammonium hydroxide (Et 4} NOH, tetraethylammonium hydroxide) (20wt% aqueous, 5 mL) was added and stirred for 30 minutes. Thereafter, Pd(PPh ₃ ) ₄ (90.1 mg, 0.078 mmol) dissolved in toluene was added to carry out a Suzuki reaction. After the reaction was terminated by endcapping, the solid produced by precipitation in methanol was filtered to obtain a copolymer 2 . The weight average molecular weight of copolymer 2 was found to be 35 to 54 kg/mol.

manufacturing example 7. Synthesis of Comparative Copolymers

Monomer 5 (2,2 '- (9,9- dioctyl-9 H -fluorene-2,7-diyl) bis (4,4,5,5-tetramethyl-1,3,2-dioxaborolane)) (1 g , 1.56 mmol), Monomer 6 4-bromo- N -(4-bromophenyl) -N -phenylaniline (439.4 mg, 1.09 mmol) and Monomer 7 4,4'-(2,5-dibromo-1,4-phenylene) bis(oxy)bis(methylene)bis(vinylbenzene) (260.3 mg. 0.47 mmol) was dissolved in toluene. The temperature was raised to 90 ℃ _{, tetraethylammonium hydroxide (Et 4} NOH, tetraethylammonium hydroxide) (20wt% aqueous, 5 mL) was added and stirred for 30 minutes. Thereafter, Pd(PPh ₃ ) ₄ (90.1 mg, 0.078 mmol) dissolved in toluene was added to carry out a Suzuki reaction. After the reaction was terminated by endcapping, the solid produced by precipitation in methanol was filtered to obtain a comparative copolymer. The weight average molecular weight of the comparative copolymer was measured to be 91 kg/mol.

Example One.

A glass substrate on which indium tin oxide (ITO) was deposited to a thickness of 1500 Å was placed in distilled water in which detergent was dissolved and washed with ultrasonic waves. After washing ITO for 30 minutes, ultrasonic washing was performed for 10 minutes by repeating twice with distilled water. After washing with distilled water, ultrasonic washing with a solvent of isopropyl alcohol and acetone was performed for 30 minutes each and dried, and then the substrate was transported to a glove box.

PEDOT:PSS was spin-coated on the prepared ITO transparent electrode to form a hole injection layer with a thickness of 300 Å, and the coating composition was cured on a hot plate in air for 1 hour.

Then, after transferring to a glove box, the copolymer 1 was dissolved in a toluene solution (2wt%) on the hole injection layer to form a hole transport layer at a thickness of 200 Å. The coating composition was cured on a hotplate for 30 minutes.

Then, the following compounds A and B were vacuum-deposited to a thickness of 300 Å at a concentration of 8 wt% on the hole transport layer to form a light emitting layer. On the light emitting layer, the following compound C was vacuum deposited to a thickness of 200 Å to form an electron injection and transport layer. A cathode was formed by depositing LiF with a thickness of 0.5 nm and aluminum with a thickness of 100 nm on the electron transport layer.

In the above process, the deposition rate of the organic material was maintained at 0.4 to 0.7 Å/sec, the deposition rate of LiF of the cathode was maintained at 0.3 Å/sec, and the deposition rate of aluminum was maintained at 2 Å/sec, and the vacuum degree during deposition was 2x10 ^-7 to 3x10 ^-5 torr was maintained.

Example 2.

An organic light emitting diode was manufactured in the same manner as in Example 1, except that Copolymer 2 was used instead of Copolymer 1 in Example 1.

comparative example One.

An organic light emitting diode was manufactured in the same manner as in Example 1, except that Comparative Copolymer was used instead of Copolymer 1 in Example 1.

The Examples 1 to 2 and Comparative Example 1 were measured for the driving voltage, current efficiency and quantum efficiency (QE) and a brightness value of an organic light emitting device at a current density of 10mA / cm ^2, manufactured by, and the current density of 10mA / cm ² The time (T90) at which it becomes 90% of the initial luminance was measured. The results are shown in Table 1 below.

device Driving voltage (V) current efficiency
(cd/A) QE (%) luminance
(Cd/m ² ) Life T90
(10mA/cm ² ) Example 1 5.97 4.79 4.56 475.2 49.3 Example 2 6.13 4.88 4.84 487.0 46.8 Comparative Example 1 6.71 5.02 5.03 514.7 36.8

Comparative Example 1 does not include a structure corresponding to Formula 1 of the present invention. It is possible to break the long conjugation chain of the copolymer comprising the formula of the present invention with an alkyl chain between the silicone and the silicone. In addition, in the case of silicon having a large atomic size, high stacking that may occur between aryl groups can be prevented, thereby increasing the solubility of the copolymer.

Therefore, the silicone structure of the present invention brings about a synergistic effect of solubility in the formation of the copolymer. It can be confirmed from the results of Table 1 that Examples 1 and 2, in which the organic light emitting device was manufactured using the compound of the present application, had lower driving voltage and superior lifespan characteristics than the organic light emitting device manufactured in Comparative Example 1.

1: substrate
2: first electrode
3: organic layer
4: light emitting layer
5: second electrode

Claims (12)

A copolymer comprising a unit of Formula 1 below, and a unit of Formula 2 below:
[Formula 1]

[Formula 2]

In Formulas 1 and 2,

means a site bonded to another substituent, monomer or bonding portion,
R1 to R6 are hydrogen; heavy hydrogen; halogen group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group,
Ar1 to Ar5 are the same as or different from each other, and each independently a direct bond; a substituted or unsubstituted arylene group; Or a substituted or unsubstituted heteroarylene group,
Ar6 and Ar7 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; a substituted or unsubstituted alkyl group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heteroaryl group,
a is an integer from 1 to 8,
b is 0 or 1,
When a is plural, the structures in parentheses are the same as or different from each other. The method according to claim 1, wherein the copolymer further comprises one or two or more of the units of formula (3), and units of formula (4):
[Formula 3]

[Formula 4]

In Formulas 3 and 4,
R7 to R10 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; halogen group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted aryloxy group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted amine group; a substituted or unsubstituted silyl group; a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group, a thermosetting group or a photocurable group,
c is an integer from 0 to 6, and when c is plural, R9 is the same as or different from each other,
d is an integer from 0 to 4, and when d is plural, R10 is the same as or different from each other. 3. The method according to claim 2,
The copolymer is a copolymer comprising one or two or more units represented by the following Chemical Formulas 1-1 to 1-3:
[Formula 1-1]

[Formula 1-2]

[Formula 1-3]

In Formulas 1-1 to 1-3,
Ar1 to Ar7, R1 to R10, and a to d are as defined in Formulas 1 to 4. 3. The method according to claim 2,
The copolymer is a copolymer comprising one or two or more units represented by the following Chemical Formulas 1-4 to 1-6:
[Formula 1-4]

[Formula 1-5]

[Formula 1-6]

In Formulas 1-4 to 1-6,
Ar1 to Ar7, R1 to R6, R10, a, b, and d are as defined in Formulas 1 to 4. The copolymer of claim 1 , wherein the copolymer comprises any one or more of the following structures:

In the structural formula,
o to q are the molar ratios of each unit, and when o+p+q=1,
o is a molar ratio of 0.025 to 0.95,
p is a molar ratio of 0.025 to 0.95,
q is a molar ratio of 0.025 to 0.95. The copolymer according to claim 1, wherein the copolymer has a number average molecular weight of 1,000 g/mol to 1,000,000 g/mol. A coating composition comprising the copolymer according to any one of claims 1 to 6. a first electrode;
a second electrode provided to face the first electrode; and
One or more organic material layers are included between the first electrode and the second electrode,
At least one layer of the organic material layer is an organic light emitting device comprising the coating composition of claim 7 or a cured product thereof. 9. The method of claim 8,
The organic layer includes a hole transport layer, a hole injection layer, or a layer that simultaneously transports and injects holes,
The hole transport layer, the hole injection layer, or the layer for transporting and injecting holes at the same time is an organic light emitting device comprising the coating composition or a cured product thereof. 9. The method of claim 8,
The organic layer includes an electron injection layer, an electron transport layer, or a layer that simultaneously injects and transports electrons,
The electron injection layer, the electron transport layer, or the layer for simultaneously injecting and transporting electrons is an organic light emitting device comprising the coating composition or a cured product thereof. preparing a substrate;
forming a cathode or an anode on the substrate;
forming one or more organic material layers on the cathode or anode; and forming an anode or a cathode on the organic material layer, wherein the forming of the organic material layer comprises forming one or more organic material layers using the coating composition of claim 7 . The method according to claim 11, wherein the step of forming the organic material layer formed by using the coating composition comprises a drying step after applying the coating composition.

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