Patent Application
20220340585
The present specification relates to a heterocyclic compound, and an organic light emitting device including the same.
The present specification claims priority to and the benefits of Korean Patent Application No. 10-2019-0088238, filed with the Korean Intellectual Property Office on Jul. 22, 2019, the entire contents of which are incorporated herein by reference.
An electroluminescent device is one type of self-emissive display devices, and has an advantage of having a wide viewing angle, and a high response speed as well as having an excellent contrast.
An organic light emitting device has a structure disposing an organic thin film between two electrodes. When a voltage is applied to an organic light emitting device having such a structure, electrons and holes injected from the two electrodes bind and pair in the organic thin film, and light emits as these annihilate. The organic thin film may be formed in a single layer or a multilayer as necessary.
A material of the organic thin film may have a light emitting function as necessary. For example, as a material of the organic thin film, compounds capable of forming a light emitting layer themselves alone may be used, or compounds capable of performing a role of a host or a dopant of a host-dopant-based light emitting layer may also be used. In addition thereto, compounds capable of performing roles of hole injection, hole transfer, electron blocking, hole blocking, electron transfer, electron injection and the like may also be used as a material of the organic thin film.
Development of an organic thin film material has been continuously required for enhancing performance, lifetime or efficiency of an organic light emitting device.
The present specification is directed to providing a heterocyclic compound, and an organic light emitting device including the same.
One embodiment of the present specification provides a heterocyclic compound represented by the following Chemical Formula 1.
In Chemical Formula 1,
X is O or S,
L is a direct bond; a substituted or unsubstituted C6 to C60 arylene group; or a substituted or unsubstituted C2 to C60 heteroarylene group,
Z and R1 are each independently a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C2 to C60 alkenyl group; a substituted or unsubstituted C2 to C60 alkynyl group; a substituted or unsubstituted C3 to C60 cycloalkyl group; a substituted or unsubstituted C2 to C60 heterocycloalkyl group; a substituted or unsubstituted C6 to C60 aryl group; a substituted or unsubstituted C2 to C60 heteroaryl group; a substituted or unsubstituted C1 to C20 alkylamine group; a substituted or unsubstituted C6 to C60 arylamine group; a substituted or unsubstituted C2 to C60 heteroarylamine group; or a substituted or unsubstituted phosphine oxide group,
R2 to R7 are each independently hydrogen; deuterium; a halogen group; a cyano group; a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C3 to C60 cycloalkyl group; a substituted or unsubstituted C6 to C60 aryl group; or a substituted or unsubstituted C2 to C60 heteroaryl group,
a is 1 or 2,
b is an integer of 1 to 3,
m and n are each an integer of 1 to 5, and
when a, b, m and n are each 2 or greater, substituents in the parentheses are the same as or different from each other.
Another embodiment of the present application provides an organic light emitting device including a first electrode; a second electrode provided opposite to the first electrode; and an organic material layer provided between the first electrode and the second electrode, wherein the organic material layer includes the heterocyclic compound represented by Chemical Formula 1.
Another embodiment of the present application provides an organic light emitting device including a first electrode; a first stack provided on the first electrode and including a first light emitting layer; a charge generation layer provided on the first stack; a second stack provided on the charge generation layer and including a second light emitting layer; and a second electrode provided on the second stack, wherein the charge generation layer includes the heterocyclic compound represented by Chemical Formula 1.
A compound described in the present specification can be used as a material of an organic material layer of an organic light emitting device. In the organic light emitting device, the compound is capable of performing a role of a hole injection material, a hole transfer material, a light emitting material, an electron transfer material, an electron injection material or the like. Particularly, the compound can be used as an electron transfer layer material or a charge generation layer material of an organic light emitting device.
Particularly, Chemical Formula 1 has a structure in which dibenzofuran or dibenzothiophene is fused to quinoline, and HOMO and LUMO levels can be adjusted by having various substituents in the benzene ring which is not fused to the quinoline in the dibenzofuran or dibenzothiophene. Accordingly, electrical properties of the structure can be enhanced by adjusting an energy band gap. In addition, electron transfer capability of a material can be enhanced through substituents having strong electron migration properties.
Specifically, when using the compound represented by Chemical Formula 1 in an organic material layer, a driving voltage of the device can be lowered, light efficiency can be enhanced, and lifetime properties of the device can be enhanced.
Hereinafter, the present specification will be described in more detail.
In the present specification, a certain part “including” certain constituents means capable of further including other constituents, and does not exclude other constituents unless particularly stated on the contrary.
In the present specification, the term “substitution” means a hydrogen atom bonding to a carbon atom of a compound being changed to another substituent, and the position of substitution is not limited as long as it is a position at which the hydrogen atom is substituted, that is, a position at which a substituent can substitute, and when two or more substituents substitute, the two or more substituents may be the same as or different from each other.
In the present specification, a “T1 value” means an energy level value in a triplet state.
In the present specification, “substituted or unsubstituted” means being substituted with one or more substituents selected from the group consisting of a halogen group; a cyano group; a C1 to C60 linear or branched alkyl group; a C2 to C60 linear or branched alkenyl group; a C2 to C60 linear or branched alkynyl group; a C3 to C60 monocyclic or polycyclic cycloalkyl group; a C2 to C60 monocyclic or polycyclic heterocycloalkyl group; a C6 to C60 monocyclic or polycyclic aryl group; a C2 to C60 monocyclic or polycyclic heteroaryl group; a silyl group; a phosphine oxide group; and an amine group, or being unsubstituted, or being substituted with a substituent linking two or more substituents selected from among the substituents illustrated above, or being unsubstituted.
In the present specification, the halogen may be fluorine, chlorine, bromine or iodine.
In the present specification, the alkyl group includes linear or branched having 1 to 60 carbon atoms, and may be further substituted with other substituents. The number of carbon atoms of the alkyl group may be from 1 to 60, specifically from 1 to 40 and more specifically from 1 to 20. Specific examples thereof may include a methyl group, an ethyl group, a propyl group, an n-propyl group, an isopropyl group, a butyl group, an n-butyl group, an isobutyl group, a tert-butyl group, a sec-butyl group, a 1-methyl-butyl group, a 1-ethyl-butyl group, a pentyl group, an n-pentyl group, an isopentyl group, a neopentyl group, a tert-pentyl group, a hexyl group, an n-hexyl group, a 1-methylpentyl group, a 2-methylpentyl group, a 4-methyl-2-pentyl group, a 3,3-dimethylbutyl group, a 2-ethylbutyl group, a heptyl group, an n-heptyl group, a 1-methylhexyl group, a cyclopentylmethyl group, a cyclohexylmethyl group, an octyl group, an n-octyl group, a tert-octyl group, a 1-methylheptyl group, a 2-ethylhexyl group, a 2-propylpentyl group, an n-nonyl group, a 2,2-dimethylheptyl group, a 1-ethyl-propyl group, a 1,1-dimethyl-propyl group, an isohexyl group, a 2-methylpentyl group, a 4-methylhexyl group, a 5-methylhexyl group and the like, but are not limited thereto.
In the present specification, the alkenyl group includes linear or branched having 2 to 60 carbon atoms, and may be further substituted with other substituents. The number of carbon atoms of the alkenyl group may be from 2 to 60, specifically from 2 to 40 and more specifically from 2 to 20. Specific examples thereof may include a vinyl group, a 1-propenyl group, an isopropenyl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group, a 1-pentenyl group, a 2-pentenyl group, a 3-pentenyl group, a 3-methyl-1-butenyl group, a 1,3-butadienyl group, an allyl group, a 1-phenylvinyl-1-yl group, a 2-phenylvinyl-1-yl group, a 2,2-diphenylvinyl-1-yl group, a 2-phenyl-2-(naphthyl-1-yl)vinyl-1-yl group, a 2,2-bis(diphenyl-1-yl)vinyl-1-yl group, a stilbenyl group, a styrenyl group and the like, but are not limited thereto.
In the present specification, the alkynyl group includes linear or branched having 2 to 60 carbon atoms, and may be further substituted with other substituents. The number of carbon atoms of the alkynyl group may be from 2 to 60, specifically from 2 to 40 and more specifically from 2 to 20.
In the present specification, the cycloalkyl group includes monocyclic or polycyclic having 3 to 60 carbon atoms, and may be further substituted with other substituents. Herein, the polycyclic means a group in which the cycloalkyl group is directly linked to or fused with other cyclic groups. Herein, the other cyclic groups may be a cycloalkyl group, but may also be different types of cyclic groups such as a heterocycloalkyl group, an aryl group and a heteroaryl group. The number of carbon groups of the cycloalkyl group may be from 3 to 60, specifically from 3 to 40 and more specifically from 5 to 20. Specific examples thereof may include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a 3-methylcyclopentyl group, a 2,3-dimethylcyclopentyl group, a cyclohexyl group, a 3-methylcyclohexyl group, a 4-methylcyclohexyl group, a 2,3-dimethylcyclohexyl group, a 3,4,5-trimethylcyclohexyl group, a 4-tert-butylcyclohexyl group, a cycloheptyl group, a cyclooctyl group and the like, but are not limited thereto.
In the present specification, the heterocycloalkyl group includes O, S, Se, N or Si as a heteroatom, includes monocyclic or polycyclic having 2 to 60 carbon atoms, and may be further substituted with other substituents. Herein, the polycyclic means a group in which the heterocycloalkyl group is directly linked to or fused with other cyclic groups. Herein, the other cyclic groups may be a heterocycloalkyl group, but may also be different types of cyclic groups such as a cycloalkyl group, an aryl group and a heteroaryl group. The number of carbon atoms of the heterocycloalkyl group may be from 2 to 60, specifically from 2 to 40 and more specifically from 3 to 20.
In the present specification, the aryl group includes monocyclic or polycyclic having 6 to 60 carbon atoms, and may be further substituted with other substituents. Herein, the polycyclic means a group in which the aryl group is directly linked to or fused with other cyclic groups. Herein, the other cyclic groups may be an aryl group, but may also be different types of cyclic groups such as a cycloalkyl group, a heterocycloalkyl group and a heteroaryl group. The aryl group includes a spiro group. The number of carbon atoms of the aryl group may be from 6 to 60, specifically from 6 to 40 and more specifically from 6 to 25. Specific examples of the aryl group may include a phenyl group, a biphenyl group, a triphenyl group, a naphthyl group, an anthryl group, a chrysenyl group, a phenanthrenyl group, a perylenyl group, a fluoranthenyl group, a triphenylenyl group, a phenalenyl group, a pyrenyl group, a tetracenyl group, a pentacenyl group, a fluorenyl group, an indenyl group, an acenaphthylenyl group, a benzofluorenyl group, a spirobifluorenyl group, a 2,3-dihydro-1H-indenyl group, a fused ring thereof, and the like, but are not limited thereto.
In the present specification, the silyl group is a substituent including Si, having the Si atom directly linked as a radical, and is represented by —SiR104R105R106. R104 to R106 are the same as or different from each other, and may be each independently a substituent formed with at least one of hydrogen; deuterium; a halogen group; an alkyl group; an alkenyl group; a cycloalkyl group; an aryl group; and a heterocyclic group. Specific examples of the silyl group may include a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a vinyldimethylsilyl group, a propyldimethylsilyl group, a triphenylsilyl group, a diphenylsilyl group, a phenylsilyl group and the like, but are not limited thereto.
In the present specification, the fluorenyl group may be substituted, and adjacent substituents may bond to each other to form a ring.
When the fluorenyl group is substituted,
and the like may be included, however, the structure is not limited thereto.
In the present specification, the heteroaryl group includes O, S, Se, N or Si as a heteroatom, includes monocyclic or polycyclic having 2 to 60 carbon atoms, and may be further substituted with other substituents. Herein, the polycyclic means a group in which the heteroaryl group is directly linked to or fused with other cyclic groups. Herein, the other cyclic groups may be a heteroaryl group, but may also be different types of cyclic groups such as a cycloalkyl group, a heterocycloalkyl group and an aryl group. The number of carbon atoms of the heteroaryl group may be from 2 to 60, specifically from 2 to 40 and more specifically from 3 to 25. Specific examples of the heteroaryl group may include a pyridyl group, a pyrrolyl group, a pyrimidyl group, a pyridazinyl group, a furanyl group, a thiophene group, an imidazolyl group, a pyrazolyl group, an oxazolyl group, an isoxazolyl group, a thiazolyl group, an isothiazolyl group, a triazolyl group, a furazanyl group, an oxadiazolyl group, a thiadiazolyl group, a dithiazolyl group, a tetrazolyl group, a pyranyl group, a thiopyranyl group, a diazinyl group, an oxazinyl group, a thiazinyl group, a dioxynyl group, a triazinyl group, a tetrazinyl group, a quinolyl group, an isoquinolyl group, a quinazolinyl group, an isoquinazolinyl group, a qninozolinyl group, a naphthyridyl group, an acridinyl group, a phenanthridinyl group, an imidazopyridinyl group, a diazanaphthalenyl group, a triazaindene group, an indolyl group, an indolizinyl group, a benzothiazolyl group, a benzoxazolyl group, a benzimidazolyl group, a benzothiophene group, a benzofuran group, a dibenzothiophene group, a dibenzofuran group, a carbazolyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a phenazinyl group, a dibenzosilole group, spirobi(dibenzosilole), a dihydrophenazinyl group, a phenoxazinyl group, a phenanthridyl group, an imidazopyridinyl group, a thienyl group, an indolo[2,3-a]carbazolyl group, an indolo[2,3-b]carbazolyl group, an indolinyl group, a 10,11-dihydro-dibenzo[b,f]azepine group, a 9,10-dihydroacridinyl group, a phenanthrazinyl group, a phenothiathiazinyl group, a phthalazinyl group, a naphthylidinyl group, a phenanthrolinyl group, a benzo[c][1,2,5]thiadiazolyl group, a 5,10-dihydrobenzo[b,e][1,4]azasilinyl group, a pyrazolo[1,5-c]quinazolinyl group, a pyrido[1,2-b]indazolyl group, a pyrido[1,2-a]imidazo[1,2-e]indolinyl group, a 5,11-dihydroindeno[1,2-b]carbazolyl group and the like, but are not limited thereto.
In the present specification, the phosphine oxide group may be specifically substituted with an aryl group, and examples described above may be applied to the aryl group. Examples of the phosphine oxide group may include a diphenylphosphine oxide group, a dinaphthylphosphine oxide group and the like, but are not limited thereto.
In the present specification, the amine group may be selected from the group consisting of a monoalkylamine group; a monoarylamine group; a monoheteroarylamine group; —NH2; a dialkylamine group; a diarylamine group; a diheteroarylamine group; an alkylarylamine group; an alkylheteroarylamine group; and an arylheteroarylamine group, and although not particularly limited thereto, the number of carbon atoms is preferably from 1 to 30. Specific examples of the amine group may include a methylamine group, a dimethylamine group, an ethylamine group, a diethylamine group, a phenylamine group, a naphthylamine group, a biphenylamine group, a dibiphenylamine group, an anthracenylamine group, a 9-methyl-anthracenylamine group, a diphenylamine group, a phenylnaphthylamine group, a ditolylamine group, a phenyltolylamine group, a triphenylamine group, a biphenylnaphthylamine group, a phenylbiphenylamine group, a biphenylfluorenylamine group, a phenyltriphenylenylamine group, a biphenyltriphenylenylamine group and the like, but are not limited thereto.
In the present specification, the structures illustrated as the aryl group and the heteroaryl group described above may be used as the arylene group and the heteroarylene group except that they are not a monovalent group.
In the present specification, an “adjacent” group may mean a substituent substituting an atom directly linked to an atom substituted by the corresponding substituent, a substituent sterically most closely positioned to the corresponding substituent, or another substituent substituting an atom substituted by the corresponding substituent. For example, two substituents substituting ortho positions in a benzene ring, and two substituents substituting the same carbon in an aliphatic ring may be interpreted as groups “adjacent” to each other.
As an aliphatic or aromatic hydrocarbon ring or heteroring that adjacent groups may form, the structures illustrated as the cycloalkyl group, the heterocycloalkyl group, the aryl group and the heteroaryl group described above may be applied except for those that are not a monovalent group.
One embodiment of the present specification provides a heterocyclic compound represented by Chemical Formula 1. Particularly, Chemical Formula 1 has a structure in which dibenzofuran or dibenzothiophene is fused to quinoline, and HOMO and LUMO levels can be adjusted by having various substituents in the benzene ring which is not fused to the quinoline in the dibenzofuran or dibenzothiophene. Accordingly, electrical properties of the structure may be enhanced by adjusting an energy band gap. In addition, electron transfer capability of a material may be enhanced through substituents having strong electron migration properties.
In one embodiment of the present specification, X is O or S.
In one embodiment of the present specification, X is O.
In another embodiment, X is S.
In one embodiment of the present specification, L is a direct bond; a substituted or unsubstituted C6 to C60 arylene group; or a substituted or unsubstituted C2 to C60 heteroarylene group.
By the Z substituent and the core structure being separated by L in the compound, hole migration properties of the core structure and electron migration properties of the substituent are distinguished in the electron cloud distribution of the molecule. This is an excellent bipolar structure facilitating electron migration, and therefore, efficiency, lifetime and driving voltage may be significantly improved.
In one embodiment of the present specification, L is a direct bond; a substituted or unsubstituted C6 to C30 arylene group; or a substituted or unsubstituted C2 to C30 heteroarylene group.
In one embodiment of the present specification, L is a direct bond; a substituted or unsubstituted phenylene group; a substituted or unsubstituted biphenylene group; a substituted or unsubstituted terphenylene group; a substituted or unsubstituted naphthylene group; a substituted or unsubstituted anthracenylene group; a substituted or unsubstituted triphenylenylene group; a substituted or unsubstituted phenanthrenylene group; a substituted or unsubstituted divalent pyridine group; a substituted or unsubstituted divalent pyrimidine group; or a substituted or unsubstituted divalent triazine group.
In one embodiment of the present specification, L is a direct bond; a phenylene group unsubstituted or substituted with an aryl group or a heteroaryl group; a biphenylene group; a terphenylene group; a naphthylene group; an anthracenylene group; a triphenylenylene group; a phenanthrenylene group; a divalent pyridine group unsubstituted or substituted with an aryl group or a heteroaryl group; a divalent pyrimidine group unsubstituted or substituted with an aryl group; or a divalent triazine group unsubstituted or substituted with an aryl group or a heteroaryl group.
In one embodiment of the present specification, L is a direct bond; a phenylene group unsubstituted or substituted with a phenyl group or a carbazole group; a biphenylene group; a terphenylene group; a naphthylene group; an anthracenylene group; a triphenylenylene group; a phenanthrenylene group; a divalent pyridine group unsubstituted or substituted with a phenyl group or a pyridine group; a divalent pyrimidine group unsubstituted or substituted with a phenyl group or a biphenyl group; or a divalent triazine group unsubstituted or substituted with a phenyl group unsubstituted or substituted with a cyano group, a biphenyl group, a naphthyl group, or a carbazole group unsubstituted or substituted with a phenyl group.
In one embodiment of the present specification, Z is a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C2 to C60 alkenyl group; a substituted or unsubstituted C2 to C60 alkynyl group; a substituted or unsubstituted C3 to C60 cycloalkyl group; a substituted or unsubstituted C2 to C60 heterocycloalkyl group; a substituted or unsubstituted C6 to C60 aryl group; a substituted or unsubstituted C2 to C60 heteroaryl group; a substituted or unsubstituted C1 to C20 alkylamine group; a substituted or unsubstituted C6 to C60 arylamine group; a substituted or unsubstituted C2 to C60 heteroarylamine group; or a substituted or unsubstituted phosphine oxide group.
In one embodiment of the present specification, Z is a substituted or unsubstituted C1 to C30 alkyl group; a substituted or unsubstituted C2 to C30 alkenyl group; a substituted or unsubstituted C2 to C30 alkynyl group; a substituted or unsubstituted C3 to C30 cycloalkyl group; a substituted or unsubstituted C2 to C30 heterocycloalkyl group; a substituted or unsubstituted C6 to C30 aryl group; a substituted or unsubstituted C2 to C30 heteroaryl group; a substituted or unsubstituted C1 to C10 alkylamine group; a substituted or unsubstituted C6 to C30 arylamine group; a substituted or unsubstituted C2 to C30 heteroarylamine group; or a substituted or unsubstituted phosphine oxide group.
In one embodiment of the present specification, Z is a substituted or unsubstituted C6 to C30 aryl group; a substituted or unsubstituted C2 to C30 heteroaryl group; or a substituted or unsubstituted phosphine oxide group.
In one embodiment of the present specification, Z is a substituted or unsubstituted phenyl group; a biphenyl group; a terphenyl group; a naphthyl group; a triphenylenyl group; a phenanthrenyl group; an anthracenyl group; a dimethylfluorenyl group; a diphenylfluorenyl group; a spirobifluorenyl group; an isoquinolinyl group; a quinazolinyl group; a phenoxazinyl group; a phenothiazinyl group; an indolocarbazole group; a substituted or unsubstituted pyridine group; a substituted or unsubstituted pyrimidine group; a substituted or unsubstituted triazine group; a substituted or unsubstituted carbazole group; a substituted or unsubstituted benzocarbazole group; a substituted or unsubstituted phenanthrolinyl group; a substituted or unsubstituted dibenzofuran group; a substituted or unsubstituted dibenzothiophene group; a substituted or unsubstituted dihydroacridine group; or a substituted or unsubstituted phosphine oxide group.
In one embodiment of the present specification, Z is a phenyl group unsubstituted or substituted with a cyano group, a phenyl group or a carbazole group; a biphenyl group; a terphenyl group; a naphthyl group; a triphenylenyl group; a phenanthrenyl group; an anthracenyl group; a dimethylfluorenyl group; a diphenylfluorenyl group; a spirobifluorenyl group; an isoquinolinyl group; a quinazolinyl group; a phenoxazinyl group; a phenothiazinyl group; an indolocarbazole group; a pyridine group unsubstituted or substituted with a phenyl group or a pyridine group; a pyrimidine group unsubstituted or substituted with a phenyl group or a biphenyl group; a triazine group unsubstituted or substituted with a phenyl group unsubstituted or substituted with a naphthyl group or a cyano group, a biphenyl group, a naphthyl group, a dimethylfluorenyl group, a dibenzofuran group, a dibenzothiophene group, or a carbazole group unsubstituted or substituted with a phenyl group; a carbazole group unsubstituted or substituted with a phenyl group; a benzocarbazole group; a phenanthrolinyl group unsubstituted or substituted with a phenyl group; a dibenzofuran group unsubstituted or substituted with a phenyl group; a dibenzothiophene group unsubstituted or substituted with a phenyl group; a dihydroacridine group unsubstituted or substituted with a methyl group or a phenyl group; or a phosphine oxide group unsubstituted or substituted with a phenyl group.
In one embodiment of the present specification, R1 is a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C2 to C60 alkenyl group; a substituted or unsubstituted C2 to C60 alkynyl group; a substituted or unsubstituted C3 to C60 cycloalkyl group; a substituted or unsubstituted C2 to C60 heterocycloalkyl group; a substituted or unsubstituted C6 to C60 aryl group; a substituted or unsubstituted C2 to C60 heteroaryl group; a substituted or unsubstituted C1 to C20 alkylamine group; a substituted or unsubstituted C6 to C60 arylamine group; a substituted or unsubstituted C2 to C60 heteroarylamine group; or a substituted or unsubstituted phosphine oxide group.
In one embodiment of the present specification, R1 is a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C3 to C60 cycloalkyl group; a substituted or unsubstituted C2 to C60 heterocycloalkyl group; a substituted or unsubstituted C6 to C60 aryl group; or a substituted or unsubstituted C2 to C60 heteroaryl group.
In one embodiment of the present specification, R1 is a substituted or unsubstituted C6 to C60 aryl group; or a substituted or unsubstituted C2 to C60 heteroaryl group.
In one embodiment of the present specification, R1 is a substituted or unsubstituted C6 to C30 aryl group; or a substituted or unsubstituted C2 to C30 heteroaryl group.
In one embodiment of the present specification, R1 is a substituted or unsubstituted C6 to C30 aryl group.
In one embodiment of the present specification, R1 is a substituted or unsubstituted phenyl group; a substituted or unsubstituted naphthyl group; a substituted or unsubstituted anthracenyl group; a substituted or unsubstituted phenanthrenyl group; a substituted or unsubstituted pyrenyl group; or a substituted or unsubstituted perylene group.
In one embodiment of the present specification, R1 is a phenyl group; a naphthyl group; an anthracenyl group; a phenanthrenyl group; a pyrenyl group; or a perylene group.
In one embodiment of the present specification, R2 to R7 are each independently hydrogen; deuterium; a halogen group; a cyano group; a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C3 to C60 cycloalkyl group; a substituted or unsubstituted C6 to C60 aryl group; or a substituted or unsubstituted C2 to C60 heteroaryl group.
In one embodiment of the present specification, R2 to R7 are each independently hydrogen; deuterium; a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C6 to C60 aryl group; or a substituted or unsubstituted C2 to C60 heteroaryl group.
In one embodiment of the present specification, R2 to R7 are each independently hydrogen; or deuterium.
In one embodiment of the present specification, R2 to R7 are hydrogen.
In one embodiment of the present specification, m may be 1 or 2.
In one embodiment of the present specification, n may be an integer of 1 to 5.
In one embodiment of the present specification, Chemical Formula 1 is represented by the following Chemical Formula 1-1.
In Chemical Formula 1-1, X, L, Z, R2 to R7, a, b, m and n have the same definitions as in Chemical Formula 1,
L′ is a direct bond; a substituted or unsubstituted C6 to C60 arylene group; or a substituted or unsubstituted C2 to C60 heteroarylene group,
Z′ is a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C3 to C60 cycloalkyl group; a substituted or unsubstituted C2 to C60 heterocycloalkyl group; a substituted or unsubstituted C6 to C60 aryl group; or a substituted or unsubstituted C2 to C60 heteroaryl group.
In one embodiment of the present specification, L′ is a direct bond.
In one embodiment of the present specification, Z′ is a substituted or unsubstituted C6 to C60 aryl group; or a substituted or unsubstituted C2 to C60 heteroaryl group.
In one embodiment of the present specification, Z′ is a substituted or unsubstituted C6 to C60 aryl group.
In one embodiment of the present specification, Z′ is a substituted or unsubstituted C6 to C30 aryl group.
In one embodiment of the present specification, Z′ is a phenyl group; a naphthyl group; an anthracenyl group; a phenanthrenyl group; a pyrenyl group; or a perylene group.
In the heterocyclic compound provided in one embodiment of the present specification, Chemical Formula 1 is represented by any one of the following Chemical Formulae 1-2 to 1-5.
In Chemical Formulae 1-2 to 1-5, X, L, Z, R1 to R7, a, b, m and n have the same definitions as in Chemical Formula 1.
In the heterocyclic compound provided in one embodiment of the present specification, Chemical Formula 1 is represented by any one of the following Chemical Formulae 2 to 4.
In Chemical Formulae 2 to 4,
X, L, Z, R1 to R7, a, b, m and n have the same definitions as in Chemical Formula 1.
In one embodiment of the present specification, Chemical Formula 1 may be represented by any one of the following compounds, but is not limited thereto.
In addition, by introducing various substituents to the structure of Chemical Formula 1, compounds having unique properties of the introduced substituents may be synthesized. For example, by introducing substituents normally used as hole injection layer materials, hole transfer layer materials, light emitting layer materials, electron transfer layer materials and charge generation layer materials used for manufacturing an organic light emitting device to the core structure, materials satisfying conditions required for each organic material layer may be synthesized.
In addition, by introducing various substituents to the structure of Chemical Formula 1, the energy band gap may be finely adjusted, and by the high T1 value obtained therefrom, an organic light emitting device with superior efficiency may be provided.
One embodiment of the present specification provides an organic light emitting device including a first electrode; a second electrode; and an organic material layer provided between the first electrode and the second electrode, wherein the organic material layer includes the heterocyclic compound represented by Chemical Formula 1.
In one embodiment of the present specification, the first electrode may be an anode, and the second electrode may be a cathode.
In another embodiment of the present specification, the first electrode may be a cathode, and the second electrode may be an anode.
In one embodiment of the present specification, the organic light emitting device may be a blue organic light emitting device, and the heterocyclic compound according to Chemical Formula 1 may be used as a material of the blue organic light emitting device. For example, the heterocyclic compound according to Chemical Formula 1 may be included in a host material of a light emitting layer of the blue organic light emitting device.
In another embodiment of the present specification, the organic light emitting device may be a green organic light emitting device, and the heterocyclic compound according to Chemical Formula 1 may be used as a material of the green organic light emitting device. For example, the heterocyclic compound according to Chemical Formula 1 may be included in a host material of a light emitting layer of the green organic light emitting device.
In another embodiment of the present specification, the organic light emitting device may be a red organic light emitting device, and the heterocyclic compound according to Chemical Formula 1 may be used as a material of the red organic light emitting device. For example, the heterocyclic compound according to Chemical Formula 1 may be included in a host material of a light emitting layer of the red organic light emitting device.
Specific descriptions on the heterocyclic compound represented by Chemical Formula 1 are the same as the descriptions provided above.
The organic light emitting device of the present specification may be manufactured using common organic light emitting device manufacturing methods and materials except that one or more of the organic material layers are formed using the heterocyclic compound described above.
The heterocyclic compound may be formed into an organic material layer through a solution coating method as well as a vacuum deposition method when manufacturing the organic light emitting device. Herein, the solution coating method means spin coating, dip coating, inkjet printing, screen printing, a spray method, roll coating and the like, but is not limited thereto.
The organic material layer of the organic light emitting device of the present specification may be formed in a single layer structure, but may be formed in a multilayer structure in which two or more organic material layers are laminated. For example, the organic light emitting device of the present disclosure may have a structure including a hole injection layer, a hole transfer layer, a light emitting layer, an electron transfer layer, an electron injection layer and the like as the organic material layer. However, the structure of the organic light emitting device is not limited thereto, and may include a smaller number of organic material layers.
In the organic light emitting device of the present specification, the organic material layer includes an electron transfer layer, and the electron transfer layer may include the heterocyclic compound of Chemical Formula 1. When using the heterocyclic compound as an electron transfer material, HOMO and LUMO may be adjusted depending on the substituent position, and excellent electron transfer efficiency is obtained. In addition, compared to existing electron transfer materials, migration of electrons in a reverse direction is prevented due to a difference in the T1 value, and as a result, superior device efficiency is obtained.
The organic light emitting device of the present disclosure may further include one, two or more layers selected from the group consisting of a light emitting layer, a hole injection layer, a hole transfer layer, an electron injection layer, an electron transfer layer, an electron blocking layer and a hole blocking layer.
The organic material layer including the heterocyclic compound represented by Chemical Formula 1 may further include other materials as necessary.
The organic light emitting device according to one embodiment of the present specification includes a first electrode; a first stack provided on the first electrode and including a first light emitting layer; a charge generation layer provided on the first stack; a second stack provided on the charge generation layer and including a second light emitting layer; and a second electrode provided on the second stack, wherein the charge generation layer may include the heterocyclic compound represented by Chemical Formula 1.
The organic light emitting device according to one embodiment of the present specification includes a first electrode; a second electrode; and an organic material layer provided between the first electrode and the second electrode, wherein the organic material layer includes two or more stacks, and the two or more stacks each independently include a light emitting layer, a charge generation layer is included between the two or more stacks, and the charge generation layer may include the heterocyclic compound represented by Chemical Formula 1.
The organic light emitting device according to one embodiment of the present specification includes a first electrode; a second electrode; and an organic material layer provided between the first electrode and the second electrode, wherein the organic material layer includes a first stack including a first light emitting layer; a charge generation layer provided on the first stack; and a second stack including a second light emitting layer, and the charge generation layer may include the heterocyclic compound represented by Chemical Formula 1.
In addition, the organic light emitting device according to one embodiment of the present specification includes an anode, a cathode, and two or more stacks provided between the anode and the cathode, the two or more stacks each independently include a light emitting layer, a charge generation layer is included between the two or more stacks, and the charge generation layer includes the heterocyclic compound represented by Chemical Formula 1.
In addition, the organic light emitting device according to one embodiment of the present specification includes an anode, a first stack provided on the anode and including a first light emitting layer, a charge generation layer provided on the first stack, a second stack provided on the charge generation layer and including a second light emitting layer, and a cathode provided on the second stack. Herein, the charge generation layer may include the heterocyclic compound represented by Chemical Formula 1. When the heterocyclic compound is included in the charge generation layer, superior efficiency as a charge generation layer material is obtained by an electron-friendly substituent structure and a hole migration-friendly quinoline-dibenzofuran or quinoline-dibenzothiophene fused structure.
The organic light emitting device according to one embodiment of the present specification includes a first electrode; a first stack provided on the first electrode and including a first light emitting layer; a charge generation layer provided on the first stack; a second stack provided on the charge generation layer and including a second light emitting layer; and a second electrode provided on the second stack, wherein the charge generation layer is an N-type charge generation layer, and the charge generation layer may include the heterocyclic compound represented by Chemical Formula 1.
In addition, the first stack and the second stack may each independently further include one or more types of the hole injection layer, the hole transfer layer, the hole blocking layer, the electron transfer layer, the electron injection layer and the like described above.
The charge generation layer may be an N-type charge generation layer or a P-type charge generation layer, and the charge generation layer may further include a dopant known in the art in addition to the heterocyclic compound represented by Chemical Formula 1.
As the organic light emitting device according to one embodiment of the present specification, an organic light emitting device having a 2-stack tandem structure is illustrated in
Herein, the first electron blocking layer, the first hole blocking layer, the second hole blocking layer and the like described in
In the organic light emitting device according to one embodiment of the present specification, materials other than the heterocyclic compound represented by Chemical Formula 1 are illustrated below, however, these are for illustrative purposes only and not for limiting the scope of the present application, and the materials may be replaced by materials known in the art.
As the anode material, materials having relatively large work function may be used, and transparent conductive oxides, metals, conductive polymers or the like may be used. Specific examples of the anode material 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); combinations of metals and oxides such as ZnO:Al or SnO2:Sb; conductive polymers such as poly(3-methylthiophene), poly[3,4-(ethylene-1,2-dioxy)thiophene](PEDOT), polypyrrole and polyaniline, and the like, but are not limited thereto.
As the cathode material, materials having relatively small work function may be used, and metals, metal oxides, conductive polymers or the like may be used. Specific examples of the cathode material include metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin and lead, or alloys thereof; multilayer structure materials such as LiF/Al or LiO2/Al, and the like, but are not limited thereto.
As the hole injection material, known hole injection materials may be used, and for example, phthalocyanine compounds such as copper phthalocyanine disclosed in U.S. Pat. No. 4,356,429, or starburst-type amine derivatives such as tris(4-carbazoyl-9-ylphenyl)amine (TCTA), 4,4′,4″-tri[phenyl(m-tolyl)amino]triphenylamine (m-MTDATA) or 1,3,5-tris[4-(3-methylphenylphenylamino)phenyl]benzene (m-MTDAPB) described in the literature [Advanced Material, 6, p. 677 (1994)], polyaniline/dodecylbenzene sulfonic acid, poly(3,4-ethylenedioxythiophene)/poly(4-styrenesulfonate), polyaniline/camphor sulfonic acid or polyaniline/poly(4-styrenesulfonate) that are conductive polymers having solubility, and the like, may be used.
As the hole transfer material, pyrazoline derivatives, arylamine-based derivatives, stilbene derivatives, triphenyldiamine derivatives and the like may be used, and low molecular or high molecular materials may also be used.
As the electron transfer material, metal complexes of oxadiazole derivatives, anthraquinodimethane and derivatives thereof, benzoquinone and derivatives thereof, naphthoquinone and derivatives thereof, anthraquinone and derivatives thereof, tetracyanoanthraquinodimethane and derivatives thereof, fluorenone derivatives, diphenyldicyanoethylene and derivatives thereof, diphenoquinone derivatives, 8-hydroxyquinoline and derivatives thereof, and the like, may be used in addition to the heterocyclic compound, and high molecular materials may also be used as well as low molecular materials.
As examples of the electron injection material, LiF is typically used in the art, however, the present application is not limited thereto.
As the light emitting material, red, green or blue light emitting materials may be used, and as necessary, two or more light emitting materials may be mixed and used. Herein, two or more light emitting materials may be used by being deposited as individual sources of supply or by being premixed and deposited as one source of supply. In addition, fluorescent materials may also be used as the light emitting material, however, phosphorescent materials may also be used. As the light emitting material, materials emitting light by bonding electrons and holes injected from an anode and a cathode, respectively, may be used alone, however, materials having a host material and a dopant material involving in light emission together may also be used.
When mixing light emitting material hosts, same series hosts may be mixed, or different series hosts may be mixed. For example, any two or more types of materials among n-type host materials or p-type host materials may be selected and used as a host material of a light emitting layer.
The organic light emitting device according to one embodiment of the present specification may be a top-emission type, a bottom-emission type or a dual-emission type depending on the materials used.
The heterocyclic compound according to one embodiment of the present specification may also be used in an organic electronic device including an organic solar cell, an organic photo conductor, an organic transistor and the like under a similar principle used in the organic light emitting device.
Hereinafter, the present specification will be described in more detail with reference to examples, however, these are for illustrative purposes only, and the scope of the present application is not limited thereto.
1) Preparation of Compound 1-1
After dissolving 1-bromo-8-chlorodibenzo[b,d]furan (100 g, 0.3552 mol) and 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (77.8 g, 0.3552 mol) in toluene, ethanol and H2O (2000 mL:200 mL:200 mL), Pd(PPh3)4 (tetrakis(triphenylphosphine)palladium(0)) (20.5 g, 0.017 mol) and NaHCO3 (89 g, 1.06 mol) were introduced thereto, and the result was stirred for 3 hours at 100° C. After the reaction was completed, methylene chloride (MC) and distilled water were introduced to the reaction solution, and the result was extracted, then dried with anhydrous MgSO4, and the solvent was removed using a rotary evaporator to obtain Compound 1-1 (77 g, 74%) in a liquid form.
2) Preparation of Compound 1-2
Compound 1-1 (77 g, 0.262 mol) and triethylamine (86 mL, 0.393 mol) were introduced to methylene chloride (1200 mL) and dissolved therein. To the mixture, benzoyl chloride (55 g, 0.393 mol) dissolved in methylene chloride (300 mL) was slowly added dropwise at 0° C. After the reaction was completed, white solids in the reaction solution were filtered and washed with hexane. These were dried to obtain Compound 1-2 (86 g, 83%) in a solid form.
3) Preparation of Compound 1-3
After dissolving Compound 1-2 (86 g, 0.216 mol) in nitrobenzene (1500 mL), POCl3 (30 mL, 0.324 mol) was slowly added dropwise thereto, and the result was reacted for 15 hours at 140° C. After the reaction was completed, a solution obtained by dissolving NaHCO3 in distilled water was slowly introduced to the reaction solution, and the result was stirred. Solids produced after that were filtered and collected, and the collected solids were recrystallized in MC and MeOH to obtain Compound 1-3 (41 g, 51%) in a solid form.
4) Preparation of Compound 1-4
After dissolving Compound 1-3 (41 g, 0.1079 mol) in 1,4-dioxane (800 mL), Pd2(dba)3 (tris(dibenzylideneacetone)dipalladium(0)) (9.8 g, 0.0107 mol), XPhos (2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl) (5.1 g, 0.0107 mol) and KOAc (potassium acetate) (31 g, 0.3237 mol) were dissolved therein, and the result was reacted for 4 hours at 90° C. After the reaction was completed, water and methylene chloride were introduced to the reaction solution, and the result was extracted. Solids obtained after that were dried, and recrystallized with methylene chloride and methanol to obtain Compound 1-4 (30 g, 60%) in a solid form.
5) Preparation of Compound 4
After dissolving Compound 1-4 (6.4 g, 0.017 mol) and 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine (7.4 g, 0.017 mol) in 1,4-dioxane:H2O=100 mL:20 mL, Pd(PPh3)4 (1.96 g, 0.0017 mol) and K3PO4 (20.8 g, 0.051 mol) were introduced thereto, and the result was stirred for 5 hours at 100° C. After the reaction was completed, solids produced in the reaction solution were washed with 1,4-dioxane and H2O. After that, only the solids were purified using a recrystallization method in dichlorobenzene (DCB) to obtain Compound 4 (6.6 g, 60%). [Preparation Example 2] Preparation of Compound 88
1) Preparation of Compound 1-1
Compound 1-1 was the same as Compound 1-1 of Preparation Example 1.
2) Preparation of Compound 2-2
Compound 1-1 (77 g, 0.262 mol) and triethylamine (86 mL, 0.393 mol) were introduced to MC (1200 mL) and dissolved therein. To the mixture, 1-pyrenecarbonyl chloride (104 g, 0.393 mol) dissolved in methylene chloride (300 mL) was slowly added dropwise at 0° C. After the reaction was completed, white solids in the reaction solution were filtered and washed with hexane. These were dried to obtain Compound 2-2 (75 g, 67%) in a solid form.
3) Preparation of Compound 2-3
After dissolving Compound 2-2 (86 g, 0.143 mol) in nitrobenzene (1500 mL), POCl3 (20 mL, 0.215 mol) was slowly added dropwise thereto, and the result was reacted for 15 hours at 140° C. After the reaction was completed, a solution obtained by dissolving NaHCO3 in distilled water was slowly introduced to the reaction solution, and the result was stirred. Solids produced after that were filtered and collected, and the collected solids were recrystallized in methylene chloride and methanol to obtain Compound 2-3 (29 g, 41%) in a solid form.
4) Preparation of Compound 2-4
After dissolving Compound 2-3 (29 g, 0.057 mol) in 1,4-dioxane (800 mL), Pd2(dba)3 (5.2 g, 0.0057 mol), XPhos (2.7 g, 0.0057 mol) and KOAc (16.7 g, 0.171 mol) were dissolved therein, and the result was reacted for 4 hours at 90° C. After the reaction was completed, water and MC were introduced to the reaction solution, and the result was extracted. After that, solids obtained by drying the result were recrystallized with methylene chloride and methanol to obtain Compound 2-4 (20 g, 60%) in a solid form.
5) Preparation of Compound 88
After dissolving Compound 2-4 (10 g, 0.017 mol) and 4-(3-bromophenyl)dibenzo[b,d]thiophene (5.7 g, 0.017 mol) in 1,4-dioxane:H2O=100 mL:20 mL, Pd(PPh3)4 (1.96 g, 0.0017 mol) and K3PO4 (20.8 g, 0.051 mol) were introduced thereto, and the result was stirred for 5 hours at 100° C. After the reaction was completed, solids produced in the reaction solution were washed with 1,4-dioxane and H2O. After that, only the solids were purified using a recrystallization method in dichlorobenzene (DCB) to obtain Compound 88 (4.9 g, 40%).
Target compounds were synthesized in the same manner as in Preparation Example 1 except that Intermediate A of the following Table 1 was used instead of 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine.
Target compounds were synthesized in the same manner as in Preparation Example 2 except that Intermediate 1 of the following Table 2 was used instead of 1-pyrenecarbonyl chloride, and Intermediate B of the following Table 2 was used instead of 4-(3-bromophenyl)dibenzo[b,d]thiophene.
Target compounds were synthesized in the same manner as in Preparation Example 1 except that 6-bromo-2-chlorodibenzo[b,d]furan was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate C of the following Table 3 was used instead of 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine.
Target compounds were synthesized in the same manner as in Preparation Example 2 except that Intermediate 2 of the following Table 4 was used instead of 1-pyrenecarbonyl chloride, 6-bromo-2-chlorodibenzo[b,d]furan was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate D of the following Table 4 was used instead of 4-3 bromophenyl)dibenzo[b,d]thiophene.
A target compound was synthesized in the same manner as in Preparation Example 1 except that 2-bromo-8-chlorodibenzo[b,d]furan was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate E of the following Table 5 was used instead of 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine.
A target compound was synthesized in the same manner as in Preparation Example 2 except that Intermediate 3 of the following Table 6 was used instead of 1-pyrenecarbonyl chloride, 2-bromo-8-chlorodibenzo[b,d]furan was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate F of the following Table 6 was used instead of 4-(3-bromophenyl)dibenzo[b,d]thiophene.
Target compounds were synthesized in the same manner as in Preparation Example 1 except that 1-bromo-6-chlorodibenzo[b,d]furan was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate G of the following Table 7 was used instead of 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine.
A target compound was synthesized in the same manner as in Preparation Example 2 except that Intermediate 4 of the following Table 8 was used instead of 1-pyrenecarbonyl chloride, 1-bromo-6-chlorodibenzo[b,d]furan was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate H of the following Table 8 was used instead of 4-3 bromophenyl)dibenzo[b,d]thiophene.
Target compounds were synthesized in the same manner as in Preparation Example 1 except that 4,6-dibromodibenzo[b,d]furan was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate I of the following Table 9 was used instead of 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine.
Target compounds were synthesized in the same manner as in Preparation Example 2 except that Intermediate 5 of the following Table 10 was used instead of 1-pyrenecarbonyl chloride, 4,6-dibromodibenzo[b,d]furan was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate I of the following Table 10 was used instead of 4-(3-bromophenyl)dibenzo[b,d]thiophene.
Target compounds were synthesized in the same manner as in Preparation Example 1 except that 1-chloro-6-fluorodibenzo[b,d]furan was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate J of the following Table 11 was used instead of 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine.
Target compounds were synthesized in the same manner as in Preparation Example 1 except that 7-chloro-1-fluorodibenzo[b,d]furan was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate K of the following Table 12 was used instead of 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine.
Target compounds were synthesized in the same manner as in Preparation Example 1 except that 1-bromo-8-chlorodibenzo[b,d]thiophene was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate L of the following Table 13 was used instead of 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine.
Target compounds were synthesized in the same manner as in Preparation Example 2 except that Intermediate 6 of the following Table 14 was used instead of 1-pyrenecarbonyl chloride, 1-bromo-8-chlorodibenzo[b,d]thiophene was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate M of the following Table 14 was used instead of 4-(3-bromophenyl)dibenzo[b,d]thiophene.
Target compounds were synthesized in the same manner as in Preparation Example 1 except that 2-bromo-8-chlorodibenzo[b,d]thiophene was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate N of the following Table 15 was used instead of 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine.
Target compounds were synthesized in the same manner as in Preparation Example 1 except that 6-bromo-2-chlorodibenzo[b,d]thiophene was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate O of the following Table 16 was used instead of 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine.
Target compounds were synthesized in the same manner as in Preparation Example 2 except that Intermediate 7 of the following Table 17 was used instead of 1-pyrenecarbonyl chloride, 6-bromo-2-chlorodibenzo[b,d]thiophene was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate P of the following Table 17 was used instead of 4-(3-bromophenyl)dibenzo[b,d]thiophene.
Target compounds were synthesized in the same manner as in Preparation Example 1 except that 1-bromo-6-chlorodibenzo[b,d]thiophene was used instead of 1-bromo-8-chlorodibenzo[b,d]furan, and Intermediate Q of the following Table 18 was used instead of 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine.
Synthesis identification results for the compounds prepared as above are shown in the following Table 19.
1) Manufacture of Organic Light Emitting Device
A transparent indium tin oxide (ITO) electrode thin film obtained from glass for an OLED (manufactured by Samsung-Corning Co., Ltd.) was ultrasonic cleaned using trichloroethylene, acetone, ethanol and distilled water consecutively for 5 minutes each, stored in isopropanol, and used.
Next, an ITO substrate was installed in a substrate folder of a vacuum deposition apparatus, and the following 4,4′,4″-tris(N,N-(2-naphthyl)-phenylamino)triphenylamine (2-TNATA) was introduced to a cell in the vacuum deposition apparatus.
Subsequently, the chamber was evacuated until the degree of vacuum therein reached 10−6 torr, and then 2-TNATA was evaporated by applying a current to the cell to deposit a hole injection layer having a thickness of 600 Å on the ITO substrate.
To another cell of the vacuum deposition apparatus, the following N,N′-bis(α-naphthyl)-N,N′-diphenyl-4,4′-diamine (NPB) was introduced, and evaporated by applying a current to the cell to deposit a hole transfer layer having a thickness of 300 Å on the hole injection layer.
After forming the hole injection layer and the hole transfer layer as above, a blue light emitting material having a structure as below was deposited thereon as a light emitting layer. Specifically, in one side cell in the vacuum deposition apparatus, H1, a blue light emitting host material, was vacuum deposited to a thickness of 200 Å, and D1, a blue light emitting dopant material, was vacuum deposited thereon by 5% with respect to the host material.
Subsequently, a compound of the following Structural Formula E1 was deposited to a thickness of 300 Å as an electron transfer layer.
As an electron injection layer, lithium fluoride (LiF) was deposited to a thickness of 10 Å, and an Al cathode was employed to a thickness of 1,000 Å, and as a result, an OLED was manufactured.
Meanwhile, all the organic compounds required to manufacture the OLED were vacuum sublimation purified under 10−8 torr to 10−6 torr by each material to be used in the OLED manufacture.
Organic electroluminescent devices were manufactured in the same manner as in Comparative Example 1 except that Compound A, Compound B, Compound C and Compound D were used instead of E1 used when forming the electron transfer layer.
Organic electroluminescent devices were manufactured in the same manner as in Comparative Example 1 except that compounds listed in the following Table 20 were used instead of E1 used when forming the electron transfer layer.
Results of measuring driving voltage, light emission efficiency, color coordinate (CIE) and lifetime of each of the blue organic light emitting devices manufactured according to the present disclosure are as shown in the following Table 20.
As seen from Table 20, the organic light emitting device using the compound of the present disclosure as an electron transfer layer material of a blue organic light emitting device had lower driving voltage and improved light emission efficiency and lifetime compared to Comparative Example 1, Comparative Example 2, Comparative Example 3 and Comparative Example 4. Such results are due to the fact that the compound is a bipolar type having both a p-type and an n-type, and therefore, hole leakage is prevented and electrons are effectively injected to a light emitting layer.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2019-0088238 | Jul 2019 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2020/009424 | 7/17/2020 | WO |
