Patent Application
20230140927
The present invention relates to a highly efficient organic light-emitting device that exhibits remarkably improved luminous efficacy using a polycyclic aromatic derivative compound in an organic layer therein.
An organic light-emitting device is a self-luminous device that emits light when energy is released from excitons which are formed by recombination of electrons injected from an electron injection electrode (cathode) and holes injected from a hole injection electrode (anode) in a light-emitting layer. Such an organic light-emitting device attracts a great deal of attention as a next-generation light source due to applicability to full-color flat panel light-emitting displays based on advantages such as low driving voltage, high luminance, wide viewing angle, and rapid response speed thereof.
In order for the organic light-emitting device to exhibit the characteristics, the structure of the organic layer in the organic light-emitting device should be optimized, and the material constituting each organic layer, namely, a hole injection material, a hole transport material, a light-emitting material, an electron transport material, an electron injection material, or an electron blocking material should be based on stable and efficient ingredients. However, there is a continuing need to develop organic layer structures and respective materials thereof for stable and efficient organic light-emitting devices.
As such, there is a continuing need for the development of the structure of an organic light-emitting device capable of improving the luminous characteristics thereof and the development of novel materials supporting the structure.
Therefore, the present invention has been made in view of the above problems, and it is one object of the present invention to provide a highly efficient organic light-emitting device that can be operated at a low voltage and exhibits excellent external quantum efficiency based on compounds used for a light-emitting layer and compounds for a hole transport layer or a hole injection layer.
In accordance with the present invention, the above and other objects can be accomplished by the provision of an organic light-emitting device including a first electrode, a second electrode facing the first electrode, and a hole injection layer or a hole transport layer and a light-emitting layer interposed between the first electrode and the second electrode.
The organic light-emitting device according to the present invention includes (i) at least one compound represented by the following [Formula A] in the hole injection layer or the hole transport layer, and (ii) a compound represented by the following [Formula B], [Formula C] or [Formula D] in the light-emitting layer.
Details of structures of [Formula A] to [Formula D], the compounds obtained thereby, and substituents thereof will be described later.
The organic light-emitting device according to the present invention can be operated at a lower driving voltage, and exhibits excellent external quantum efficiency and thus high luminous efficacy by utilizing the compounds having characteristic structures as the hole transport material and the dopant material, respectively, in the hole injection layer or the hole transport layer, and the light-emitting layer.
Hereinafter, the present invention will be described in detail with reference to the annexed drawings.
In one aspect, the present invention is directed to an organic light-emitting device including a first electrode, a second electrode facing the first electrode, and a hole injection layer or a hole transport layer and a light-emitting layer interposed between the first electrode and the second electrode, wherein (i) the hole injection layer or the hole transport layer includes at least one compound represented by the following [Formula A] and (ii) the light-emitting layer includes a compound represented by the following [Formula B] to [Formula D]. Based on this configuration, a highly efficient organic light-emitting device can be obtained.
wherein
L is a single bond, a substituted or unsubstituted aromatic C6-C50 hydrocarbon ring, or a substituted or unsubstituted C2-C50 aromatic heterocyclic ring, and n is an integer of 1 to 3, with the proviso that when n is 2 or more, L's are identical to or different from each other.
In an embodiment, in [Formula A], L is a single bond or a substituted or unsubstituted aromatic C6-C50 hydrocarbon ring, wherein the substituted or unsubstituted aromatic C6-C50 hydrocarbon ring is a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted phenanthryl group, or a substituted or unsubstituted fluorenyl group.
Ar is selected from a substituted or unsubstituted C5-C50 aryl group and a substituted or unsubstituted C2-C50 heteroaryl group.
Ra to Rc are identical to or different from each other, and are each independently hydrogen, deuterium, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted C6-C50 aryl group, a substituted or unsubstituted C3-C30 cycloalkyl group, a substituted or unsubstituted C2-C50 heteroaryl group, a substituted or unsubstituted C1-C30 alkoxy group, a substituted or unsubstituted C6-C30 aryloxy group, a substituted or unsubstituted C1-C30 alkylthioxy group, a substituted or unsubstituted C5-C30 arylthioxy group, a substituted or unsubstituted C1-C30 alkylamine group, a substituted or unsubstituted C5-C30 arylamine group, a substituted or unsubstituted C1-C30 alkylsilyl group, a substituted or unsubstituted C5-C30 arylsilyl group, a nitro group, a cyano group, and a halogen group.
Also, Rb and Rc are bonded to each other to further form an alicyclic or aromatic monocyclic or polycyclic ring.
Next, the compounds represented by the following [Formula B] to [Formula D] used in the light-emitting layer in the organic light-emitting device according to the present invention will be described as follows.
wherein
Q1 to Q3 are identical to or different from each other, and are each independently a substituted or unsubstituted aromatic C6-C50 hydrocarbon ring, or a substituted or unsubstituted C2-050 aromatic heterocyclic group, and Y is each independently selected from N—R1, CR2R3, O, S,
Se, and SiR4R5, with the proviso that Y's are identical to or different from each other.
In an embodiment of the present invention, in [Formula B] to [Formula D], Y may be NR1.
X is selected from B, P and P═O and, in a preferred embodiment of the present invention, X is B, and in this case, a polycyclic aromatic derivative compound containing boron (B) is structurally used as a dopant in the light-emitting layer of a device to impart high efficiency to the organic light-emitting device.
R1 to R5 are identical to or different from each other, and are each independently hydrogen, deuterium, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted C6-C50 aryl group, a substituted or unsubstituted C3-C30 cycloalkyl group, a substituted or unsubstituted C2-C50 heteroaryl group, a substituted or unsubstituted C1-C30 alkoxy group, a substituted or unsubstituted C6-C30 aryloxy group, a substituted or unsubstituted C1-C30 alkylthioxy group, a substituted or unsubstituted C5-C30 arylthioxy group, a substituted or unsubstituted C1-C30 alkylamine group, a substituted or unsubstituted C5-C30 arylamine group, a substituted or unsubstituted C1-C30 alkylsilyl group, a substituted or unsubstituted C5-C30 arylsilyl group, a nitro group, a cyano group, and a halogen group.
Each of R1 to R5 is bonded to the ring Q1 to Q3 to further form an alicyclic or aromatic monocyclic or polycyclic ring, and R2 and R3, and R4 and R5 are bonded to each other to further form an alicyclic or aromatic monocyclic or polycyclic ring.
In addition, in [Formula B] to [Formula D], each of Cy1, Cy2, and Cy3 represents a moiety to form a ring as follows.
Cy1 is linked to an adjacent nitrogen (N) atom and an aromatic carbon atom in the adjacent Q1 ring to form a fused ring including a nitrogen (N) atom, an aromatic carbon atom in the Q1 ring to which the nitrogen (N) atom is bonded, and an aromatic carbon atom in the Q1 ring to which Cy1 is bonded.
In addition, the fused ring formed by Cy1 is a substituted or unsubstituted C2-C5 alkylene group, provided that the nitrogen (N) atom, the aromatic carbon atom in the Q1 ring to which the nitrogen (N) atom is bonded, and the aromatic carbon atom in the Q1 ring to which Cy1 is bonded are excluded.
Cy2 is added to Cy1 to form a saturated hydrocarbon ring.
In addition, the ring formed by Cy2 is a substituted or unsubstituted C2-C5 alkylene group, provided that the carbon atom included in Cy1 is excluded.
Cy3 is linked to a carbon atom bonded to a nitrogen atom in the adjacent Cy1, and an aromatic carbon atom in the Q3 ring to form a fused ring including the aromatic carbon atom in the Q3 ring to which Cy3 is bonded, the nitrogen (N) atom and the carbon atom in Cy1 bonded to the nitrogen (N) atom.
In addition, the fused ring formed by Cy3 is a substituted or unsubstituted C1-C4 alkylene group, provided that the aromatic carbon atom in the Q3 ring to which Cy3 is bonded, the nitrogen (N) atom and the carbon atom in Cy1 bonded to the nitrogen (N) atom are excluded.
The compounds represented by [Formula B] to [Formula D] may form various polycyclic aromatic skeleton structures based on the definitions of substituents given above. The specific structures thereof can be clearly identified from specific compounds described later and a high-efficiency organic light-emitting device can be realized by satisfying the characteristics required for the compounds used for the light-emitting layer of the organic light-emitting device based thereon.
Meanwhile, as used herein, the term “substituted” indicates substitution of various substituents defined in [Formula A] to [Formula D] with one or more substituents selected from deuterium, a cyano group, a halogen group, a hydroxyl group, a nitro group, an alkyl group, a halogenated alkyl group, a cycloalkyl group, an alkenyl group, an alkynyl group, a heteroalkyl group, an aryl group, an arylalkyl group, an alkylaryl group, a heteroaryl group, a heteroarylalkyl group, an alkoxy group, an amine group, a silyl group, an aryloxy group and a mixed aliphatic-aromatic ring group, or substitution with a substituent including two or more of the substituents linked to each other. The term “unsubstituted” in the same definition indicates having no substituent.
In addition, the range of the number of the carbon atoms of the alkyl group or aryl group in the term “substituted or unsubstituted C1-C30 alkyl group”, “substituted or unsubstituted C6-C50 aryl group” or the like refers to the total number of carbon atoms constituting the alkyl or aryl moiety when the corresponding group is not substituted without considering the number of carbon atoms in the substituent(s). For example, a phenyl group substituted at the para position with a butyl group corresponds to an aryl group having 6 carbon atoms substituted with a butyl group having 4 carbon atoms.
In addition, as used herein, the expression “a substituent is bonded to an adjacent substituent to form a ring” means that the corresponding substituent is bonded to the adjacent substituent to form a substituted or unsubstituted alicyclic or aromatic ring, and the term “adjacent substituent” may mean a substituent substituted for an atom which is directly attached to an atom substituted with the corresponding substituent, a substituent sterically disposed at the nearest position to the corresponding substituent, or another substituent substituted for an atom which is substituted with the corresponding substituent. For example, two substituents substituted at the ortho position in a benzene ring and two substituents substituted at the same carbon in the aliphatic ring may be considered “adjacent” to each other.
As used herein, the alkyl group may be a linear or branched alkyl group. Examples of the alkyl group include, but are not limited to, 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-methylbutyl group, a 1-ethylbutyl 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.
As used herein, the alkenyl group may include a linear or branched alkenyl group and may be further substituted with another substituent. Specifically, examples of the alkenyl group include, but are not limited to, 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.
As used herein, the alkynyl group may also include a linear or branched alkynyl group, and may be further substituted with another substituent, and examples of the substituent may include, but are not limited to, ethynyl, 2-propynyl, and the like.
As used herein, the aromatic hydrocarbon ring or the aryl group may be monocyclic or polycyclic, examples of the monocyclic aryl group include a phenyl group, a biphenyl group, a terphenyl group, a stilbene group, and the like, and examples of the polycyclic aryl group include, but are not limited to, a naphthyl group, an anthracenyl group, a phenanthrenyl group, a pyrenyl group, a perylenyl group, a tetracenyl group, a chrysenyl group, a fluorenyl group, an acenaphthcenyl group, a triphenylene group, a fluoranthene group, and the like, but the scope of the present invention is not limited thereto.
As used herein, the aromatic heterocyclic or heteroaryl group is an aromatic ring containing at least one heteroatom and examples thereof include, but are not limited to, thiophene, furan, pyrrole, imidazole, triazole, oxazole, oxadiazole, triazole, pyridyl, bipyridyl, pyrimidyl, triazine, triazole, acridyl, pyridazine, pyrazinyl, quinolinyl, quinazoline, quinoxalinyl, phthalazinyl, pyridopyrimidinyl, pyridopyrazinyl, pyrazinopyrazinyl, isoquinoline, indole, carbazole, benzoxazole, benzimidazole, benzothiazole, benzocarbazole, benzothiophene, dibenzothiophene, benzofuranyl, dibenzofuranyl, phenanthroline, thiazolyl, isoxazolyl, oxadiazolyl, thiadiazolyl, benzothiazolyl, and phenothiazinyl groups and the like.
As used herein, the aliphatic hydrocarbon ring refers to a non-aromatic ring that contains only carbon and hydrogen atoms, for example, includes a monocyclic or polycyclic ring, and may be further substituted with another substituent. The term “polycyclic” means that the polycyclic group may be directly attached to or fused with at least one other cyclic group, the other cyclic group may be an aliphatic hydrocarbon ring, or a different type of ring group, for example, an aliphatic heterocyclic group, an aryl group, a heteroaryl group, and the like. Specifically, examples thereof include, but are not limited to, cycloalkyls such as a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, an adamantyl 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, and a cyclooctyl group, cycloalkanes such as cyclohexane and cyclopentane, and cycloalkenes such as cyclohexene and cyclobutene.
As used herein, the aliphatic heterocyclic ring refers to an aliphatic ring that contains at least one of heteroatoms such as O, S, Se, N and Si, also includes a monocyclic or polycyclic ring, and may be further substituted with another substituent. The term “polycyclic” means that the polycyclic group may be directly attached to or fused with at least one other cyclic group, and the other cyclic group may be an aliphatic hydrocarbon ring, or a different type of ring group, for example, an aliphatic heterocyclic group, an aryl group, a heteroaryl group, or the like.
As used herein, the mixed aliphatic-aromatic ring group refers to a ring in which two or more rings are attached to and fused with each other, and aliphatic and aromatic rings are fused together to be overall non-aromatic, and a polycyclic mixed aliphatic-aromatic ring may contain a heteroatom selected from N, O, P and S, in addition to C.
As used herein, specifically, the alkoxy group may be methoxy, ethoxy, propoxy, isobutyloxy, sec-butyloxy, pentyloxy, iso-amyloxy, hexyloxy, or the like, but is not limited thereto.
As used herein, the silyl group is represented by —SiH3, and may be an alkylsilyl group, an arylsilyl group, an alkylarylsilyl group, an arylheteroarylsilyl group, or the like, and specific examples of the silyl group include trimethylsilyl, triethylsilyl, triphenylsilyl, trimethoxysilyl, dimethoxyphenylsilyl, diphenylmethylsilyl, diphenylvinylsilyl, methylcyclobutylsilyl, dimethylfurylsilyl, and the like.
As used herein, the amine group is represented by —NH2, or may be an alkylamine group, an arylamine group, an arylheteroarylamine group, or the like. The arylamine group refers to amine substituted with aryl, the alkylamine group refers to amine substituted with alkyl, and the arylheteroarylamine group refers to an amine substituted with aryl and heteroaryl. For example, the arylamine group includes a substituted or unsubstituted monoarylamine group, a substituted or unsubstituted diarylamine group, or a substituted or unsubstituted triarylamine group. The aryl group and the heteroaryl group in the arylamine group and the arylheteroarylamine group may be a monocyclic aryl group or a monocyclic heteroaryl group, or a polycyclic aryl group or a polycyclic heteroaryl group. The arylamine group and the arylheteroarylamine group that contain two or more aryl groups and two or more heteroaryl groups, respectively, include a monocyclic aryl group (heteroaryl group), a polycyclic aryl group (heteroaryl group), or both of the monocyclic aryl group (heteroaryl group) and the polycyclic aryl group (heteroaryl group). In addition, the aryl group and the heteroaryl group in the arylamine group and the arylheteroarylamine group may be selected from examples of aryl groups and heteroaryl groups described above.
As used herein, examples of the aryl group in the aryloxy group and the arylthioxy group are identical to examples of the aryl group described above and specifically, examples of the aryloxy group include a phenoxy group, a p-tolyloxy group, an m-tolyloxy group, a 3,5-dimethylphenoxy group, a 2,4,6-trimethylphenoxy group, a p-tert-butylphenoxy group, a 3-biphenyloxy group, a 4-biphenyloxy group, a 1-naphthyloxy group, a 2-naphthyloxy group, a 4-methyl-1-naphthyloxy group, a 5-methyl-2-naphthyloxy group, a 1-anthryloxy group, a 2-anthryloxy group, a 9-anthryloxy group, a 1-phenanthryloxy group, a 3-phenanthryloxy group, a 9-phenanthryloxy group, and the like, and examples of the arylthioxy group include, but are not limited to, a phenylthioxy group, a 2-methylphenylthioxy group, a 4-tert-butylphenylthioxy group, and the like.
In the present invention, examples of the halogen group include fluorine, chlorine, bromine, and iodine.
More specifically, the compound represented by [Formula A] according to the present invention is selected from the following [Compound 1] to [Compound 255], which clearly show specific substituents, but these compounds should not be construed as limiting the scope of [Formula A] according to the present invention.
In addition, more specifically, the polycyclic aromatic derivative compound represented by one of [Formula B] to [Formula D] according to the present invention, used as the dopant for the light-emitting layer, is selected from the following compounds, which clearly show specific substituents, but these compounds should not be construed as limiting the scope of [Formula B] to [Formula D] according to the present invention.
As can be seen from the specific compounds, an organic light-emitting material having the intrinsic properties of the substituent can be synthesized, in particular, a dopant material used in the light-emitting layer can be prepared by forming a polycyclic aromatic structure including B, P, and P═O and introducing substituents therein and a highly efficient organic light-emitting device can be realized by applying the compound represented by [Formula A] according to the present invention to the device.
In addition, in another aspect, the present invention is directed to an organic light-emitting device including a first electrode, a second electrode, and a hole injection layer and/or a hole transport layer and a light-emitting layer interposed between the first electrode and the second electrode, and the organic light-emitting device may be fabricated using a conventional method and materials for fabricating devices using the compound of [Formula A] in the hole injection layer, the hole transport layer, and a functional layer capable of injecting and/or transporting holes, and the compounds of [Formula B] to [Formula D] as dopants in the light-emitting layer.
In addition to the light-emitting layer, the hole injection layer, the hole transport layer, and the functional layer capable of injecting and/or transporting holes, the organic light-emitting device according to the present invention may further include an electron transport layer, an electron injection layer, an electron blocking layer, a hole blocking layer, and the like, and the organic light-emitting device may use materials for the respective layers.
Specifically, the organic light-emitting device according to the present invention may use the following anthracene derivative compound as a host compound for the light-emitting layer.
The organic material layer structure of the preferred organic light-emitting device according to the present invention will be described in more detail in the following Examples.
Meanwhile, a detailed structure of the organic light-emitting device according to an embodiment of the present invention, a method of manufacturing the same, and materials for the organic layers will be described as follows.
First, a substrate is coated with a material for an anode to form the anode. The substrate used herein is a substrate generally used for organic light-emitting devices and is preferably an organic substrate or a transparent plastic substrate that has excellent transparency, surface evenness, handleability and waterproofness. In addition, a material for the anode is indium tin oxide (ITO), indium zinc oxide (IZO), tin oxide (SnO2), zinc oxide (ZnO), or the like, which is transparent and has excellent conductivity.
A hole injection layer is formed on the anode by vacuum thermal evaporation or spin coating using a material for the hole injection layer, and then a hole transport layer is formed on the hole injection layer by vacuum thermal evaporation or spin coating using a material for the hole transport layer.
The material for the hole injection layer may be used without particular limitation as long as it is commonly used in the art and specific examples thereof include 2-TNATA [4,4′,4″-tris(2-naphthylphenyl-phenylamino)-triphenylamine], NPD [N,N′-di(1-naphthyl)-N,N′-diphenylbenzidine)], TPD [N,N′-diphenyl-N,N′-bis(3-methylphenyl)-1,1′-biphenyl-4,4′-diamine], DNTPD [N,N′-diphenyl-N,N′-bis-[4-(phenyl-m-tolyl-amino)-phenyl]-biphenyl-4,4′-diamine], and the like.
In addition, the material for the hole transport layer is also used without particular limitation as long as it is commonly used in the art and is, for example, N,N′-bis(3-methylphenyl)-N,N′-diphenyl-[1,1-biphenyl]-4,4′-diamine (TPD) or N,N′-di(naphthalen-1-yl)-N,N′-diphenylbenzidine (α-NPD).
Subsequently, a hole auxiliary layer and a light-emitting layer are sequentially stacked on the hole transport layer, and a hole blocking layer is selectively deposited on the light-emitting layer by vacuum deposition or spin coating to form a thin film. Because the lifetime and efficiency of the device are reduced when holes are introduced into the cathode through the organic light-emitting layer, the hole blocking layer is formed using a material having a very low HOMO (highest occupied molecular orbital) level so as to prevent this problem. The hole blocking material used herein is not particularly limited and is typically BAlq, BCP or TPBI that has an electron transport ability and has an ionization potential higher than that of a light-emitting compound.
The material used for the hole blocking layer may be BAlq, BCP, Bphen, TPBI, NTAZ, BeBq2, OXD-7, Liq, or the like, but is not limited thereto.
An electron transport layer is deposited on the hole blocking layer through vacuum deposition or spin coating and a metal for forming a cathode is formed on the electron injection layer through vacuum thermal evaporation to form a cathode. As a result, an organic light-emitting device according to an embodiment is completed.
Here, the metal for forming the cathode may be lithium (Li), magnesium (Mg), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In), magnesium-silver (Mg—Ag) or the like. A transmissive cathode using ITO or IZO may be used in order to obtain a top-emission type light-emitting device.
The material for the electron transport layer functions to stably transport electrons injected from the cathode and may be a well-known electron transport material. Examples of the well-known electron transport material include quinoline derivatives, especially, tris(8-quinolinolate)aluminum (Alq3), TAZ, BAlq, beryllium bis(benzoquinolin-10-olate: Bebq2) and oxadiazole derivatives (PBD, BMD, BND, etc.).
In addition, each of the organic layers may be formed by a monomolecular deposition or solution process. The deposition is a method of forming a thin film by evaporating a material for forming each layer through heating in the presence of a vacuum or low pressure and the solution process is a method of forming a thin film by mixing a material for forming each layer with a solvent and forming the thin film from the mixture through a method such as inkjet printing, roll-to-roll coating, screen printing, spray coating, dip coating, or spin coating.
In addition, the organic light-emitting device according to the present invention may further include a light-emitting layer of a blue light-emitting material, a green light-emitting material, or a red light-emitting material that emits light in a wavelength range of 380 nm to 800 nm. That is, the light-emitting layer of the present invention includes a plurality of light-emitting layers, and a blue light-emitting material, a green light-emitting material, or a red light-emitting material in the additionally formed light-emitting layer may be a fluorescent material or a phosphorescent material.
In addition, the organic light-emitting device is used for a display or lighting system selected from flat panel displays, flexible displays, monochromatic or white flat panel lighting systems, monochromatic or white flexible lighting systems, vehicle displays, and displays for virtual or augmented reality.
Hereinafter, the present invention will be described in more detail with reference to preferred examples. However, it will be obvious to those skilled in the art that these examples are merely provided for illustration of the present invention, and should not be construed as limiting the scope of the present invention.
100 g (0.924 mol) of phenylhydrazine and 500 mL of acetic acid were stirred in a round-bottom flask and then heated to 60° C. 103.6 g (0.924 mol) of 2-methyl cyclohexanone was slowly added dropwise, followed by refluxing for 8 hours. After completion of the reaction, the reaction product was extracted with water and ethyl acetate, concentrated and separated by column chromatography to obtain 130 g of <Intermediate 1-a>. (yield 76%)
75 g (405 mmol) of <Intermediate 1-a> was added to a round-bottom flask containing 750 mL of toluene under a nitrogen atmosphere, cooled to −10° C., and then 380 mL (608 mmol) of 1.6 M methyl lithium was slowly added dropwise, followed by stirring at −10° C. for about 3 hours. After completion of the reaction, the product was extracted with water and ethyl acetate, concentrated and separated by column chromatography to obtain 50.5 g of <Intermediate 1-b>. (yield 62%)
50 g (251 mmol) of <intermediate 1-b>, 56.7 g (251 mmol) of 1-bromo-2,3-dichlorobenzene, 4.5 g (5 mmol) of tris(dibenzylideneacetone)dipalladium, 2 g (10 mmol) of tritertiary butylphosphine, 35.8 g (373 mmol) of sodium tertiary butoxide, and 500 mL of toluene were added to a round-bottom flask under a nitrogen atmosphere, followed by refluxing for 24 hours. After completion of the reaction, the organic layer was concentrated under reduced pressure and separated by column chromatography to obtain 35.6 g of <Intermediate 1-c>. (yield 41%)
<Intermediate 1-d> was obtained in the same manner as in Synthesis Example 1-3, except that diphenylamine was used instead of <Intermediate 1-b> and <Intermediate 1-c> was used instead of 1-bromo-2,3-dichlorobenzene in Synthesis Example 1-3. (yield 73%)
20 g (42 mmol) of <Intermediate 1-d> was added to a round-bottom flask containing 200 mL of tert-butylbenzene under a nitrogen atmosphere, cooled to −30° C., and 49.1 mL (84 mmol) of a 1.7 M tert-butyllithium pentane solution was slowly added dropwise. After completion of the dropwise addition, the temperature was raised to 60° C., followed by stirring for 3 hours and removal of pentane through distillation. The residue was cooled to −50° C., 20.8 g (84 mmol) of boron tribromide was added dropwise thereto, and the mixture was warmed to room temperature, followed by stirring for 1 hour. The reaction product was cooled to 0° C. again, and 10.7 g (84 mmol) of N,N-diisopropylethylamine was added thereto, followed by stirring at 120° C. for 3 hours. After completion of the reaction, tert-butylbenzene was removed by distillation under reduced pressure, extracted with water and ethyl acetate, and concentrated by column chromatography to obtain 5.3 g of <Compound 1>. (yield 28%)
MS (MALDI-TOF): m/z 452.24 [M−]
<Intermediate 2-a> was obtained in the same manner as in Synthesis Example 1-3, except that 2,3-dimethyl-2,3-dihydro-1H-indole was used instead of <Intermediate 1-b> in Synthesis Example 1-3. (yield 52%)
<Intermediate 2-b> was obtained in the same manner as in Synthesis Example 1-3, except that N1,N2,N3-triphenylbenzene-1,3,-diamine was used instead of <Intermediate 1-b> and <Intermediate 2-a> was used instead of 1-bromo-2,3-dichlorobenzene. (yield 55%)
<Formula 33> was obtained in the same manner as in Synthesis Example 1-5, except that <Intermediate 2-b> was used instead of <Intermediate 1-d>. (yield 68%)
<Formula 95> was obtained in the same manner as in Synthesis Example 1-4, except that N1,N2,N3-triphenyl-1,3-benzenediamine was used instead of diphenylamine. (yield 17%)
MS(MALDI-TOF): m/z 619.32 [M+]
3-bromo-9-phenyl-9H-carbazole (11.3 g, 0.035 mol), 4-aminobiphenyl (6.6 g, 0.039 mol), tris(dibenzylideneacetone)dipalladium (0) (0.65 g, 0.0007 mol), sodium tert-butoxide (6.79 g, 0.0706 mol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (0.44 g, 0.0007 mol) and 100 mL of toluene were added to a round-bottom flask, followed by stirring under reflux for 3 hours. After completion of the reaction, the mixture was cooled to room temperature and extracted with ethyl acetate and water. The organic layer was separated, dehydrated with magnesium sulfate, and then concentrated under reduced pressure. The result was separated by column chromatography to obtain 12.2 g of <Intermediate 11-a>. (yield 85%)
3-bromo-9,9-dimethylfluorene (2.4 g, 0.009 mol), <Intermediate 11-a> (5.3 g, 0.013 mol), palladium (II) acetate (0.08 g, 0.4 mmol), sodium tert-butoxide (3.4 g, 0.035 mol), tri-tert-butylphosphine (0.07 g, 0.4 mmol), and 60 mL of toluene were added to a round-bottom flask, followed by stirring under reflux for 2 hours. After completion of the reaction, the reaction solution was cooled to room temperature and extracted with ethyl acetate and water. The organic layer was separated, dehydrated with magnesium sulfate, and then concentrated under reduced pressure. The result was separated and purified by column chromatography and recrystallized with dichloromethane and acetone to obtain 2.6 g of <Compound 12>. (yield 48%)
MS (MALDI-TOF): m/z 602.27 [M−]
<Compound 30> was synthesized in the same manner as in Synthesis Example 11 except that 1-naphthylamine was used instead of 4-aminobiphenyl used in Synthesis Example 11-(1), and 3-bromo-9,9-dimethylfluorene was used instead of 2-bromo-9,9-dimethylfluorene used in Synthesis Example 11-(2) (yield 45%).
MS (MALDI-TOF): m/z 830.29 [M−]
<Compound 44> was synthesized in the same manner as in Synthesis Example 11 except that aniline-2,3,4,5,6-d5 was used instead of 4-aminobiphenyl used in Synthesis Example 11-(1), and 2-bromo-9,9′-dimethylfluorene was used instead of 2-bromo-9,9-dimethylfluorene used in Synthesis Example 11-(2) (yield 46%).
MS (MALDI-TOF): m/z 653.29 [M+]
<Compound 78> was synthesized in the same manner as in Synthesis Example 11 except that 2-bromo-9,9-diphenylfluorene was used instead of 2-bromo-9,9-dimethylfluorene used in Synthesis Example 11-(2) (yield 46%).
MS (MALDI-TOF): m/z 726.30 [M+]
<Compound 102> was synthesized in the same manner as in Synthesis Example 11, except that 2-naphthylamine was used instead of 4-aminobiphenyl used in Synthesis Example 11-(1) and 2-(4-bromophenyl)-9,9-diphenyl-9H-fluorene was used instead of 2-bromo-9,9-dimethylfluorene used in Synthesis Example 11-(2) (yield 45%).
MS (MALDI-TOF): m/z 776.32 [M+]
<Compound 174> was synthesized in the same manner as in Synthesis Example 11, except that 3-bromo-9-phenyl-9H-carbazole was used instead of 2-bromo-9-phenyl-9H-carbazole used in Synthesis Example 11-(1), and 4-(1-naphthyl)aniline was used instead of 4-aminobiphenyl (yield 47%).
MS (MALDI-TOF): m/z 652.29 [M+]
<Compound 195> was synthesized in the same manner as in Synthesis Example 11, except that 3-bromo-9-phenyl-9H-carbazole was used instead of 2-bromo-9-phenyl-9H-carbazole used in Synthesis Example 11-(1), 3-aminobiphenyl was used instead of 4-aminobiphenyl, and 1-(4-bromophenyl)-9,9-dimethyl-9H-fluorene was used instead of 2-bromo-9,9-dimethylfluorene used in Synthesis Example 11-(2) (yield 45%).
MS (MALDI-TOF): m/z 678.30 [M+]
ITO glass was patterned such that a light-emitting area of the ITO glass was adjusted to 2 mm×2 mm and was then washed. The ITO glass was mounted in a vacuum chamber, a base pressure was set to 1×10−7 torr, and 2-TNATA (400 Å) and a material for a hole transport layer shown in [Table 1] (200 Å) were sequentially deposited on the ITO glass. Then, a mixture of [BH] as a host and the compound shown in the following Table 1 as a dopant (3 wt %) was deposited to a thickness of 250 Å to form a light-emitting layer. Then, a compound of [Formula E-1] was deposited thereon to a thickness of 300 Å to form an electron transport layer, Liq was deposited thereon to a thickness of 10 Å to form an electron injection layer, and Al was deposited thereon to a thickness of 1,000 Å to form a cathode. As a result, an organic light-emitting device was fabricated. The properties of the organic light-emitting device were measured at 10 mA/cm2.
Organic light-emitting devices were fabricated in the same manner as in Examples above, except that [HT] and [BD1] were used instead of the compound used as the hole transport layer material and dopant compounds, respectively, in Examples 1 to 15. The properties of the organic light-emitting devices were measured at 10 mA/cm2. The structures of [HT] and [BD1] are as follows.
As can be seen from [Table 1] above, the organic light-emitting device according to the present invention using the hole transport material (Formula A) in the hole transport layer, and using the dopant materials (Formula B/C/D) according to the present invention in the light-emitting layer can be operated at a lower voltage and exhibit improved luminous efficacy based on remarkably improved external quantum efficiency compared to the organic light-emitting device using the conventional compound represented by HT, the organic light-emitting device using the conventional compound represented by BD1, and the organic light-emitting device without using the combination of materials according to the present invention.
The organic light-emitting device according to the present invention can be operated at a lower driving voltage and exhibits excellent external quantum efficiency and thus high luminous efficacy by utilizing the compounds having characteristic structures as a hole transport material and a dopant material, respectively, in the hole injection layer or the hole transport layer, and the light-emitting layer, and thus is industrially applicable to flat panel displays, flexible displays, monochromatic or white flat panel lighting systems, monochromatic or white flexible lighting systems, vehicle displays, displays for virtual or augmented reality and the like.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2020-0033291 | Mar 2020 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2021/003379 | 3/18/2021 | WO |
