WO2020022860A1 - Nouveau composé et dispositif électroluminescent organique l'utilisant - Google Patents

Nouveau composé et dispositif électroluminescent organique l'utilisant Download PDF

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WO2020022860A1
WO2020022860A1 PCT/KR2019/009417 KR2019009417W WO2020022860A1 WO 2020022860 A1 WO2020022860 A1 WO 2020022860A1 KR 2019009417 W KR2019009417 W KR 2019009417W WO 2020022860 A1 WO2020022860 A1 WO 2020022860A1
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compound
group
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formula
added
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Korean (ko)
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정민우
이동훈
서상덕
박슬찬
황성현
장분재
이정하
한수진
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주식회사 엘지화학
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Priority claimed from KR1020190091211A external-priority patent/KR102231197B1/ko
Application filed by 주식회사 엘지화학 filed Critical 주식회사 엘지화학
Priority to EP19842262.8A priority Critical patent/EP3808744A4/fr
Priority to JP2020555215A priority patent/JP7102679B2/ja
Priority to US17/046,647 priority patent/US20210184131A1/en
Priority to CN201980028729.0A priority patent/CN112041315B/zh
Publication of WO2020022860A1 publication Critical patent/WO2020022860A1/fr

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    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/656—Aromatic compounds comprising a hetero atom comprising two or more different heteroatoms per ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers

Definitions

  • the present invention relates to a novel compound and an organic light emitting device comprising the same.
  • organic light emitting phenomenon refers to a phenomenon of converting electrical energy into light energy using an organic material.
  • the organic light emitting device using the organic light emitting phenomenon has a wide viewing angle, excellent contrast, fast response time, excellent brightness, driving voltage and response speed characteristics, many studies have been conducted.
  • the organic light emitting device generally has a structure including an anode and a cathode and an organic layer between the anode and the cathode.
  • the organic layer is often formed of a multi-layered structure composed of different materials to increase the efficiency and stability of the organic light emitting device, for example, it may be made of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer.
  • Patent Document 1 Korean Patent Publication No. 10-2000-0051826
  • the present invention relates to a novel organic light emitting material and an organic light emitting device comprising the same.
  • the present invention provides a compound represented by Formula 1:
  • X 1 to X 3 are each independently CH or N, provided that at least two of X 1 to X 3 are N,
  • Y 1 and Y 2 are each independently O or S,
  • L is a single bond; Substituted or unsubstituted C 6-60 arylene; Or C 2-60 heteroarylene containing any one or more selected from the group consisting of substituted or unsubstituted N, O and S,
  • Ar 1 is C 6-60 aryl substituted with at least one deuterium
  • Each R 1 is independently hydrogen; heavy hydrogen; halogen; Cyano; Nitro; Amino; Substituted or unsubstituted C 1-60 alkyl; Substituted or unsubstituted C 3-60 cycloalkyl; Substituted or unsubstituted C 2-60 alkenyl; Substituted or unsubstituted C 6-60 aryl; Or C 2-60 heteroaryl including one or more heteroatoms selected from the group consisting of substituted or unsubstituted N, O and S, or two adjacent R 1 's combine with each other to form a C 6-60 aromatic ring Or form a C 2-60 heteroaromatic ring comprising at least one heteroatom selected from the group consisting of N, O and S,
  • n is an integer of 0-4.
  • the present invention is a first electrode; A second electrode provided to face the first electrode; And at least one organic material layer provided between the first electrode and the second electrode, wherein at least one of the organic material layers comprises a compound represented by Chemical Formula 1. do.
  • the compound represented by Chemical Formula 1 may be used as a material of the organic material layer of the organic light emitting diode, and may improve efficiency, low driving voltage, and / or lifetime characteristics in the organic light emitting diode.
  • the compound represented by Chemical Formula 1 may be used as a hole injection, hole transport, hole injection and transport, light emission, electron transport, or electron injection material.
  • FIG. 1 shows an example of an organic light emitting element composed of a substrate 1, an anode 2, a light emitting layer 3, and a cathode 4.
  • FIG. 2 shows a substrate 1, an anode 2, a hole injection layer 5, a hole transport layer 6, an electron blocking layer 7, a light emitting layer 3, an electron transport layer 8, an electron injection layer 9.
  • an organic light emitting element composed of a cathode 4.
  • the present invention provides a compound represented by Chemical Formula 1.
  • substituted or unsubstituted is deuterium; Halogen group; Nitrile group; Nitro group; Hydroxyl group; Carbonyl group; Ester group; Imide group; Amino group; Phosphine oxide groups; An alkoxy group; Aryloxy group; Alkyl thioxy group; Arylthioxy group; Alkyl sulfoxy groups; Aryl sulfoxy group; Silyl groups; Boron group; Alkyl groups; Cycloalkyl group; Alkenyl groups; Aryl group; Aralkyl group; Ar alkenyl group; Alkylaryl group; Alkylamine group; Aralkyl amine groups; Heteroarylamine group; Arylamine group; Aryl phosphine group; Or substituted or unsubstituted with one or more substituents selected from the group consisting of heterocyclic groups including one or more of N, O, and S atoms, or two or more substituents connected to the substituents
  • a substituent to which two or more substituents are linked may be a biphenyl group. That is, the biphenyl group may be an aryl group, and can be interpreted as a substituent to which two phenyl groups are linked.
  • carbon number of a carbonyl group in this specification is not specifically limited, It is preferable that it is C1-C40. Specifically, it may be a compound having a structure as follows, but is not limited thereto.
  • the ester group may be substituted with oxygen of the ester group having 1 to 25 carbon atoms, a straight chain, branched chain or cyclic alkyl group or an aryl group having 6 to 25 carbon atoms.
  • it may be a compound of the following structural formula, but is not limited thereto.
  • carbon number of an imide group is not specifically limited, It is preferable that it is C1-C25. Specifically, it may be a compound having a structure as follows, but is not limited thereto.
  • the silyl group includes trimethylsilyl group, triethylsilyl group, t-butyldimethylsilyl group, vinyldimethylsilyl group, propyldimethylsilyl group, triphenylsilyl group, diphenylsilyl group, phenylsilyl group, and the like.
  • the present invention is not limited thereto.
  • the boron group specifically includes, but is not limited to, trimethylboron group, triethylboron group, t-butyldimethylboron group, triphenylboron group, phenylboron group and the like.
  • examples of the halogen group include fluorine, chlorine, bromine or iodine.
  • the alkyl group may be linear or branched chain, carbon number is not particularly limited, but is preferably 1 to 40. According to an exemplary embodiment, the alkyl group has 1 to 20 carbon atoms. According to another exemplary embodiment, the alkyl group has 1 to 10 carbon atoms. According to another exemplary embodiment, the alkyl group has 1 to 6 carbon atoms.
  • alkyl group examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n -Pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl , n-heptyl, 1-methylhexyl, cyclopentylmethyl, cyclohexylmethyl, octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhexyl
  • the alkenyl group may be linear or branched chain, carbon number is not particularly limited, but is preferably 2 to 40. According to an exemplary embodiment, the alkenyl group has 2 to 20 carbon atoms. According to another exemplary embodiment, the alkenyl group has 2 to 10 carbon atoms. According to another exemplary embodiment, the alkenyl group has 2 to 6 carbon atoms.
  • Specific examples include vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 3-methyl-1- Butenyl, 1,3-butadienyl, allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, 2,2-diphenylvinyl-1-yl, 2-phenyl-2- ( Naphthyl-1-yl) vinyl-1-yl, 2,2-bis (diphenyl-1-yl) vinyl-1-yl, stilbenyl group, styrenyl group and the like, but are not limited thereto.
  • the cycloalkyl group is not particularly limited, but preferably has 3 to 60 carbon atoms, and according to one embodiment, the cycloalkyl group has 3 to 30 carbon atoms. According to another exemplary embodiment, the cycloalkyl group has 3 to 20 carbon atoms. According to another exemplary embodiment, the cycloalkyl group has 3 to 6 carbon atoms.
  • the aryl group is not particularly limited, but preferably has 6 to 60 carbon atoms, and may be a monocyclic aryl group or a polycyclic aryl group. According to an exemplary embodiment, the aryl group has 6 to 30 carbon atoms. According to an exemplary embodiment, the aryl group has 6 to 20 carbon atoms.
  • the aryl group may be a phenyl group, a biphenyl group, a terphenyl group, etc. as the monocyclic aryl group, but is not limited thereto.
  • the polycyclic aryl group may be a naphthyl group, anthracenyl group, phenanthryl group, pyrenyl group, perylenyl group, chrysenyl group, fluorenyl group, and the like, but is not limited thereto.
  • a fluorenyl group may be substituted, and two substituents may be bonded to each other to form a spiro structure.
  • the fluorenyl group is substituted, And so on.
  • the present invention is not limited thereto.
  • the heterocyclic group is a heterocyclic group containing one or more of O, N, Si, and S as a dissimilar element, and the carbon number is not particularly limited, but is preferably 2 to 60 carbon atoms.
  • the heterocyclic group include thiophene group, furan group, pyrrole group, imidazole group, thiazole group, oxazole group, oxadiazole group, triazole group, pyridyl group, bipyridyl group, pyrimidyl group, triazine group, acridil group , Pyridazine group, pyrazinyl group, quinolinyl group, quinazoline group, quinoxalinyl group, phthalazinyl group, pyrido pyrimidinyl group, pyrido pyrazinyl group, pyrazino pyrazinyl group, isoquinoline group, indole group , Carbazole group
  • the aryl group in the aralkyl group, aralkenyl group, alkylaryl group, and arylamine group is the same as the example of the aryl group described above.
  • the alkyl group among the aralkyl group, the alkylaryl group, and the alkylamine group is the same as the example of the alkyl group described above.
  • the heteroaryl of the heteroarylamine may be applied to the description of the aforementioned heterocyclic group.
  • the alkenyl group in the aralkenyl group is the same as the example of the alkenyl group described above.
  • the description of the aryl group described above may be applied.
  • the description of the aforementioned heterocyclic group may be applied except that the heteroarylene is a divalent group.
  • the hydrocarbon ring is not a monovalent group, and the description of the aforementioned aryl group or cycloalkyl group may be applied except that two substituents are formed by bonding.
  • the heterocyclic group is not a monovalent group, and the description of the aforementioned heterocyclic group may be applied except that two substituents are formed by bonding.
  • Formula 1 may be represented by any one of the following Formula 2 to Formula 5:
  • X 1 to X 3 , Y 1 , Y 2 , L, Ar 1 , R 1 and n are the same as defined in Chemical Formula 1.
  • Formula 1 may be represented by any one of the following Formulas 2-1 to 5-4:
  • X 1 to X 3 , Y 1 , Y 2 , L, Ar 1 , R 1 and n are the same as defined in Chemical Formula 1.
  • X 1 to X 3 may be all N.
  • L is a single bond; Substituted or unsubstituted C 6-20 arylene; Or C 6-20 heteroarylene including any one or more selected from the group consisting of substituted or unsubstituted N, O and S,
  • L may be a single bond, phenylene, biphenylene, naphthylene, carbazolylene, dibenzofuranylene, or dibenzothiophenylene,
  • L may be a single bond.
  • Ar 1 is C 6-20 aryl substituted with at least one deuterium
  • Ar 1 may be phenyl substituted with five deuteriums.
  • R 1 is each independently hydrogen; heavy hydrogen; halogen; Cyano; Nitro; Amino; Substituted or unsubstituted C 1-10 alkyl; Substituted or unsubstituted C 3-20 cycloalkyl; Substituted or unsubstituted C 2-10 alkenyl; Substituted or unsubstituted C 6-20 aryl; Or C 6-20 heteroaryl including one or more heteroatoms selected from the group consisting of substituted or unsubstituted N, O and S, or two adjacent R 1 's combine with each other to form a C 6-20 aromatic ring Or C 2-20 heteroaromatic ring comprising at least one heteroatom selected from the group consisting of N, O and S,
  • each R 1 is independently hydrogen or phenyl, or two adjacent R 1 's may be bonded to each other to form one ring selected from the following group;
  • R 1 is each independently hydrogen or phenyl, or two adjacent R 1 are bonded to each other Can be formed.
  • n is an integer from 0 to 2.
  • Formula 1 may be represented by any one of the following Formula 1-1 or Formula 1-2:
  • X 1 to X 3 , Y 1 , Y 2 , L, Ar 1 and R 1 are as defined in Chemical Formula 1.
  • the compound represented by Chemical Formula 1 may be prepared by, for example, a manufacturing method as in Scheme 1 below, and the remaining compounds may be similarly prepared.
  • X 1 to X 3 , Y 1 , Y 2 , L, Ar 1 , R 1 and n are as defined in Formula 1, Z 1 and Z 2 are each independently halogen, preferably Z 1 and Z 2 are each independently chloro or bromo.
  • Step 1 of Scheme 1 is a Suzuki coupling reaction, preferably carried out in the presence of a palladium catalyst and a base, the reactor for the Suzuki coupling reaction can be changed as known in the art.
  • Step 2 of Scheme 1 is an amine substitution reaction, preferably carried out in the presence of a palladium catalyst and a base, the reactor for the amine substitution reaction can be changed as known in the art.
  • the manufacturing method may be more specific in the production examples to be described later.
  • the present invention provides an organic light emitting device comprising a compound represented by the formula (1).
  • the present invention is a first electrode; A second electrode provided to face the first electrode; And at least one organic material layer provided between the first electrode and the second electrode, wherein at least one of the organic material layers comprises a compound represented by Chemical Formula 1. do.
  • the organic material layer of the organic light emitting device of the present invention may be formed of a single layer structure, but may be formed of a multilayer structure in which two or more organic material layers are stacked.
  • the organic light emitting device of the present invention may have a structure including a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer and the like as an organic layer.
  • the structure of the organic light emitting device is not limited thereto and may include a smaller number of organic layers.
  • the organic layer may include a light emitting layer, and the light emitting layer includes a compound represented by Chemical Formula 1.
  • the compound according to the present invention can be used as a host of the light emitting layer.
  • the organic layer may include an electron transport layer, or an electron injection layer, the electron transport layer, or the electron injection layer comprises a compound represented by the formula (1).
  • the electron transport layer, the electron injection layer, or a layer for the electron transport and electron injection at the same time includes a compound represented by the formula (1).
  • the organic layer may include a light emitting layer and an electron transport layer
  • the electron transport layer may include a compound represented by the formula (1).
  • the organic light emitting device according to the present invention may be an organic light emitting device having a structure in which an anode, one or more organic material layers, and a cathode are sequentially stacked on a substrate.
  • the organic light emitting diode according to the present invention may be an organic light emitting diode having an inverted type structure in which a cathode, one or more organic material layers, and an anode are sequentially stacked on a substrate.
  • FIGS. 1 and 2 the structure of an organic light emitting device according to an embodiment of the present invention is illustrated in FIGS. 1 and 2.
  • FIG. 1 shows an example of an organic light emitting element composed of a substrate 1, an anode 2, a light emitting layer 3, and a cathode 4.
  • the compound represented by Formula 1 may be included in the light emitting layer.
  • the compound represented by Chemical Formula 1 may be included in one or more of the hole injection layer, the hole transport layer, the electron blocking layer, the light emitting layer, the electron transport layer and the electron injection layer.
  • the organic light emitting device according to the present invention may be manufactured by materials and methods known in the art, except that at least one layer of the organic material layer includes the compound represented by Chemical Formula 1.
  • the organic material layers may be formed of the same material or different materials.
  • the organic light emitting device may be manufactured by sequentially stacking a first electrode, an organic material layer, and a second electrode on a substrate. At this time, by using a physical vapor deposition (PVD) method such as sputtering or e-beam evaporation, a metal or conductive metal oxide or an alloy thereof is deposited on the substrate to form an anode.
  • PVD physical vapor deposition
  • an organic material layer including a hole injection layer, a hole transport layer, a light emitting layer, and an electron transport layer may be formed thereon, and then a material that may be used as a cathode may be deposited thereon.
  • an organic light emitting device may be manufactured by sequentially depositing a cathode material, an organic material layer, and an anode material on a substrate.
  • the compound represented by Chemical Formula 1 may be formed as an organic layer by a solution coating method as well as a vacuum deposition method in the manufacture of the organic light emitting device.
  • the solution coating method means spin coating, dip coating, doctor blading, inkjet printing, screen printing, spray method, roll coating, etc., but is not limited thereto.
  • an organic light emitting device may be manufactured by sequentially depositing an organic material layer and an anode material on a substrate from a cathode material (WO 2003/012890).
  • the manufacturing method is not limited thereto.
  • the first electrode is an anode
  • the second electrode is a cathode
  • the first electrode is a cathode
  • the second electrode is an anode
  • the anode material a material having a large work function is generally preferred to facilitate hole injection into the organic material layer.
  • the positive electrode 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), indium zinc oxide (IZO); Combinations of oxides with metals such as ZnO: Al or SnO 2 : Sb; Conductive polymers such as poly (3-methylthiophene), poly [3,4- (ethylene-1,2-dioxy) thiophene] (PEDOT), polypyrrole and polyaniline, and the like, but are not limited thereto.
  • the cathode material is a material having a small work function to facilitate electron injection into the organic material layer.
  • the negative electrode material include metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin, and lead or alloys thereof; Multilayer structure materials such as LiF / Al or LiO 2 / Al, and the like, but are not limited thereto.
  • the hole injection layer is a layer for injecting holes from the electrode, and has a capability of transporting holes to the hole injection material, and has a hole injection effect at the anode, an excellent hole injection effect to the light emitting layer or the light emitting material, A compound which prevents the excitons from moving to the electron injection layer or the electron injection material and is excellent in thin film formation ability is preferable.
  • the highest occupied molecular orbital (HOMO) of the hole injection material is between the work function of the positive electrode material and the HOMO of the surrounding organic layer.
  • hole injection material examples include metal porphyrin, oligothiophene, arylamine-based organic material, hexanitrile hexaazatriphenylene-based organic material, quinacridone-based organic material, and perylene-based Organic materials, anthraquinone and polyaniline and polythiophene-based conductive polymers, but are not limited thereto.
  • the hole transport layer is a layer for receiving holes from the hole injection layer and transporting holes to the light emitting layer.
  • a hole transporting material is a material capable of transporting holes from an anode or a hole injection layer and transferring them to the light emitting layer. This is suitable. Specific examples thereof include an arylamine-based organic material, a conductive polymer, and a block copolymer having a conjugated portion and a non-conjugated portion together, but are not limited thereto.
  • the electron blocking layer is a layer placed between the hole transport layer and the light emitting layer to prevent electrons injected from the cathode from being passed back to the hole transport layer without recombination in the light emitting layer.
  • the electron blocking layer is also called an electron suppression layer or an electron blocking layer. .
  • As the electron blocking layer a material having a smaller electron affinity than the electron transport layer is preferable.
  • the light emitting material is a material capable of emitting light in the visible region by transporting and combining holes and electrons from the hole transport layer and the electron transport layer, respectively, and a material having good quantum efficiency with respect to fluorescence or phosphorescence is preferable.
  • Specific examples thereof include 8-hydroxyquinoline aluminum complex (Alq 3 ); Carbazole series compounds; Dimerized styryl compounds; BAlq; 10-hydroxybenzo quinoline-metal compound; Benzoxazole, benzthiazole and benzimidazole series compounds; Poly (p-phenylenevinylene) (PPV) -based polymers; Spiro compounds; Polyfluorene, rubrene and the like, but are not limited thereto.
  • the light emitting layer may include a host material and a dopant material.
  • the host material may be a condensed aromatic ring derivative or a hetero ring-containing compound.
  • the condensed aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, and fluoranthene compounds
  • the heterocyclic containing compounds include carbazole derivatives, dibenzofuran derivatives and ladder types. Furan compounds, pyrimidine derivatives, and the like, but are not limited thereto.
  • the compound represented by Formula 1 may be included as a host material of the emission layer.
  • Dopant materials include aromatic amine derivatives, styrylamine compounds, boron complexes, fluoranthene compounds, metal complexes, and the like.
  • the aromatic amine derivatives include condensed aromatic ring derivatives having a substituted or unsubstituted arylamino group, and include pyrene, anthracene, chrysene and periplanthene having an arylamino group, and a styrylamine compound may be substituted or unsubstituted.
  • At least one arylvinyl group is substituted with the above-described arylamine, and one or two or more substituents selected from the group consisting of aryl group, silyl group, alkyl group, cycloalkyl group and arylamino group are substituted or unsubstituted.
  • substituents selected from the group consisting of aryl group, silyl group, alkyl group, cycloalkyl group and arylamino group are substituted or unsubstituted.
  • styrylamine, styryldiamine, styryltriamine, styryltetraamine and the like but is not limited thereto.
  • the metal complex includes, but is not limited to, an iridium complex, a platinum complex, and the like.
  • the electron transport layer is a layer that receives electrons from the electron injection layer and transports electrons to the light emitting layer.
  • the electron transporting material a material capable of injecting electrons well from the cathode and transferring them to the light emitting layer is suitable. Do. Specific examples include Al complexes of 8-hydroxyquinoline; Complexes including Alq 3 ; Organic radical compounds; Hydroxyflavone-metal complexes and the like, but are not limited thereto.
  • the electron transport layer can be used with any desired cathode material as used according to the prior art.
  • suitable cathode materials are conventional materials having a low work function followed by an aluminum or silver layer. Specifically cesium, barium, calcium, ytterbium and samarium, followed by aluminum layers or silver layers in each case.
  • the electron injection layer is a layer for injecting electrons from an electrode, has a capability of transporting electrons, has an electron injection effect from the cathode, excellent electron injection effect to the light emitting layer or the light emitting material, and hole injection of excitons generated in the light emitting layer
  • the compound which prevents the movement to a layer and is excellent in thin film formation ability is preferable.
  • fluorenone anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, preorenylidene methane, anthrone and the derivatives thereof, metal Complex compounds, nitrogen-containing five-membered ring derivatives, and the like, but are not limited thereto.
  • Examples of the metal complex compound include 8-hydroxyquinolinato lithium, bis (8-hydroxyquinolinato) zinc, bis (8-hydroxyquinolinato) copper, bis (8-hydroxyquinolinato) manganese, Tris (8-hydroxyquinolinato) aluminum, tris (2-methyl-8-hydroxyquinolinato) aluminum, tris (8-hydroxyquinolinato) gallium, bis (10-hydroxybenzo [h] Quinolinato) beryllium, bis (10-hydroxybenzo [h] quinolinato) zinc, bis (2-methyl-8-quinolinato) chlorogallium, bis (2-methyl-8-quinolinato) ( o-cresolato) gallium, bis (2-methyl-8-quinolinato) (1-naphtholato) aluminum, bis (2-methyl-8-quinolinato) (2-naphtolato) gallium, etc. It is not limited to this.
  • the organic light emitting device according to the present invention may be a top emission type, a bottom emission type or a double-sided emission type depending on the material used.
  • the compound represented by Formula 1 may be included in an organic solar cell or an organic transistor in addition to the organic light emitting device.
  • compound sub 1 (20.0 g, 37.9 mmol) and 9-carbazole (6.3 g, 37.9 mmol) were added to 200 mL of xylene, and sodium tert-butoxide (7.3 g, 75.7 mmol) was added thereto.
  • Bis (tri tert-butylphosphine) palladium (0.6 g, 3 mol%) was added thereto, and the mixture was stirred under reflux for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • the solid was dissolved in 1000 mL of chloroform, washed twice with water, and then the organic layer was separated, anhydrous magnesium sulfate was added thereto, stirred, and filtered. The filtrate was distilled under reduced pressure. The concentrated compound was purified through a silica column using chloroform and ethyl acetate to give a yellow solid compound 1 (13.5 g, yield 54%).
  • compound sub 2 (20.0 g, 37.9 mmol) and 9-carbazole (6.3 g, 37.9 mmol) were added to 200 mL of xylene, and dissolved with sodium tertiary-butoxide (7.3 g, 75.7 mmol). Warm up. Bis (tri tert-butylphosphine) palladium (0.6 g, 3 mol%) was added thereto, and the mixture was stirred under reflux for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • the solid was dissolved in 1000 mL of chloroform, washed twice with water, and then the organic layer was separated, anhydrous magnesium sulfate was added thereto, stirred, and filtered. The filtrate was distilled under reduced pressure. The concentrated compound was purified through a silica column using chloroform and ethyl acetate to give a green solid compound 2 (9.0 g, yield 36%).
  • the solid was dissolved in 1000 mL of chloroform, washed twice with water, and then the organic layer was separated, anhydrous magnesium sulfate was added thereto, stirred, and filtered. The filtrate was distilled under reduced pressure. The concentrated compound was purified through a silica column using chloroform and ethyl acetate to give a green solid compound 3 (13.5 g, yield 54%).
  • compound sub 4 (20.0 g, 37.9 mmol) and 9-carbazole (6.3 g, 37.9 mmol) were added to 200 mL of xylene, and sodium tert-butoxide (7.3 g, 75.7 mmol) was added thereto.
  • Bis (tri tert-butylphosphine) palladium (0.6 g, 3 mol%) was added thereto, and the mixture was stirred under reflux for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • compound sub 5 (20.0 g, 37.9 mmol) and 9-carbazole (6.3 g, 37.9 mmol) were added to 200 mL of xylene, and sodium tert-butoxide (7.3 g, 75.7 mmol) was added thereto.
  • Bis (tri tert-butylphosphine) palladium (0.6 g, 3 mol%) was added thereto, followed by stirring for 12 hours at reflux. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • the solid was dissolved in 1000 mL of chloroform, washed twice with water, and then the organic layer was separated, anhydrous magnesium sulfate was added thereto, stirred, and filtered. The filtrate was distilled under reduced pressure. The concentrated compound was purified through a silica column using chloroform and ethyl acetate to give a green solid compound 7 (10.2 g, yield 41%).
  • compound sub 8 (20.0 g, 37.9 mmol) and 9-carbazole (6.3 g, 37.9 mmol) were added to 200 mL of xylene, and sodium tert-butoxide (7.3 g, 75.7 mmol) was added thereto.
  • Bis (tri tert-butylphosphine) palladium (0.6 g, 3 mol%) was added thereto, and the mixture was stirred under reflux for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • compound sub 9 (20.0 g, 36.8 mmol) and 9-carbazole (6.1 g, 36.8 mmol) were added to 200 mL of xylene, and sodium tert-butoxide (7.1 g, 73.5 mmol) was added thereto.
  • Bis (tri tert-butylphosphine) palladium (0.6 g, 3 mol%) was added thereto, and the mixture was stirred under reflux for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • compound 10 (20.0 g, 36.8 mmol) and 9-carbazole (6.1 g, 36.8 mmol) were added to 200 mL of xylene, and dissolved with sodium tertiary-butoxide (7.1 g, 73.5 mmol).
  • Bis (tri tert-butylphosphine) palladium 0.6 g, 3 mol%) was added thereto, and the mixture was stirred under reflux for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • compound sub 11 (20.0 g, 36.8 mmol) and 9-carbazole (6.1 g, 36.8 mmol) were added to 200 mL of xylene, and sodium tert-butoxide (7.1 g, 73.5 mmol) was added thereto.
  • Bis (tri tert-butylphosphine) palladium (0.6 g, 3 mol%) was added thereto, and the mixture was stirred under reflux for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • compound sub 12 (20.0 g, 36.8 mmol) and 9-carbazole (6.1 g, 36.8 mmol) were added to 200 mL of xylene, and sodium tert-butoxide (7.1 g, 73.5 mmol) was added thereto.
  • Bis (tri tert-butylphosphine) palladium (0.6 g, 3 mol%) was added thereto, and the mixture was stirred under reflux for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • compound sub 13 (20.0 g, 37.9 mmol) and 9-carbazole (6.3 g, 37.9 mmol) were added to 200 mL of xylene, and sodium tert-butoxide (7.3 g, 75.7 mmol) was added thereto.
  • Bis (tri tert-butylphosphine) palladium (0.6 g, 3 mol%) was added thereto, followed by stirring for 12 hours at reflux. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • Dissolve compound sub 14 (20.0 g, 37.9 mmol) and 9-carbazole (6.3 g, 37.9 mmol) in 200 mL of xylene in a nitrogen atmosphere, and add sodium tertiary-butoxide (7.3 g, 75.7 mmol).
  • sodium tertiary-butoxide 7.7 g, 75.7 mmol.
  • Bis (tri tert-butylphosphine) palladium 0.6 g, 3 mol%) was added thereto, and the mixture was stirred under reflux for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • the solid was dissolved in 1000 mL of chloroform, washed twice with water, and then the organic layer was separated, anhydrous magnesium sulfate was added thereto, stirred, and filtered. The filtrate was distilled under reduced pressure. The concentrated compound was purified through a silica column using chloroform and ethyl acetate to give a green solid compound 14 (12.0 g, yield 48%).
  • compound sub 15 (20.0 g, 37.9 mmol) and 9-carbazole (6.3 g, 37.9 mmol) were added to 200 mL of xylene, and sodium tert-butoxide (7.3 g, 75.7 mmol) was added thereto.
  • Bis (tri tert-butylphosphine) palladium (0.6 g, 3 mol%) was added thereto, and the mixture was stirred under reflux for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • compound sub 16 (20.0 g, 37.9 mmol) and 9-carbazole (6.3 g, 37.9 mmol) were added to 200 mL of xylene, and sodium tert-butoxide (7.3 g, 75.7 mmol) was added thereto.
  • Bis (tri tert-butylphosphine) palladium (0.6 g, 3 mol%) was added thereto, and the mixture was stirred under reflux for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, and the produced solid was filtered.
  • a glass substrate coated with a thin film of ITO (indium tin oxide) having a thickness of 1,300 mm 3 was placed in distilled water in which detergent was dissolved and ultrasonically cleaned.
  • ITO indium tin oxide
  • Fischer Co. was used as a detergent
  • distilled water was filtered secondly as a filter of Millipore Co. as a distilled water.
  • ultrasonic washing was repeated 10 times with distilled water twice.
  • ultrasonic washing with a solvent of isopropyl alcohol, acetone, methanol dried and transported to a plasma cleaner.
  • the substrate was cleaned for 5 minutes using an oxygen plasma, and then the substrate was transferred to a vacuum evaporator.
  • the following compound HI-1 was thermally vacuum deposited to a thickness of 50 kPa on the prepared ITO transparent electrode to form a hole injection layer.
  • a hole transport layer was formed by thermal vacuum deposition of the following compound HT-1 to 250 kW on the hole injection layer, and an electron blocking layer was formed by vacuum depositing the following compound HT-2 to 50 kW on the HT-1 deposition film.
  • the following ET-1 compound was vacuum deposited to a thickness of 250 kPa on the light emitting layer to form an electron transport layer. Formed. Aluminum was deposited to a thickness of 1000 ⁇ on the electron injection layer to form a cathode.
  • the deposition rate of the organic material was maintained at 0.4 ⁇ 0.7 ⁇ / sec
  • the aluminum was maintained at the deposition rate of 2 ⁇ / sec
  • the vacuum during deposition was maintained at 1 ⁇ 10 -7 ⁇ 5 ⁇ 10 -8 torr It was.
  • An organic light-emitting device was manufactured in the same manner as in Example 1, except that Example 1 was used instead of Compound 1 of Preparation Example 7 in Table 1.
  • An organic light-emitting device was manufactured in the same manner as in Example 1, except that Example 1 was used instead of Compound 1 of Preparation Example 7 in Table 1.
  • the compounds of CE1 to CE4 in Table 1 are as follows.
  • the organic light emitting diodes were measured voltage and efficiency at a current density of 10 mA / cm 2 , and their lifetimes were measured at a current density of 50 mA / cm 2 , and the results are shown in Table 1 below.
  • LT 95 means a time when the luminance becomes 95% of the initial luminance.
  • substrate 2 anode

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Electroluminescent Light Sources (AREA)

Abstract

La présente invention concerne un nouveau composé et un dispositif électroluminescent organique le comprenant.
PCT/KR2019/009417 2018-07-27 2019-07-29 Nouveau composé et dispositif électroluminescent organique l'utilisant WO2020022860A1 (fr)

Priority Applications (4)

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EP19842262.8A EP3808744A4 (fr) 2018-07-27 2019-07-29 Nouveau composé et dispositif électroluminescent organique l'utilisant
JP2020555215A JP7102679B2 (ja) 2018-07-27 2019-07-29 新規な化合物およびこれを利用した有機発光素子
US17/046,647 US20210184131A1 (en) 2018-07-27 2019-07-29 Novel compound and organic light emitting device comprising the same
CN201980028729.0A CN112041315B (zh) 2018-07-27 2019-07-29 化合物和包含其的有机发光器件

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KR10-2018-0088202 2018-07-27
KR20180088202 2018-07-27
KR10-2019-0091211 2019-07-26
KR1020190091211A KR102231197B1 (ko) 2018-07-27 2019-07-26 신규한 화합물 및 이를 이용한 유기발광 소자

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WO2021166553A1 (fr) * 2020-02-17 2021-08-26 出光興産株式会社 Élément électroluminescent organique et appareil électronique
WO2021166552A1 (fr) * 2020-02-17 2021-08-26 出光興産株式会社 Élément électroluminescent organique et dispositif électronique
WO2021180614A1 (fr) 2020-03-11 2021-09-16 Merck Patent Gmbh Appareil électroluminescent organique
WO2021180625A1 (fr) 2020-03-11 2021-09-16 Merck Patent Gmbh Appareil électroluminescent organique
EP4019513A4 (fr) * 2019-12-20 2022-11-09 LG Chem, Ltd. Nouveau composé et diode électroluminescente organique le comprenant
CN115551853A (zh) * 2020-08-04 2022-12-30 株式会社Lg化学 新型化合物及包含其的有机发光器件

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EP4019513A4 (fr) * 2019-12-20 2022-11-09 LG Chem, Ltd. Nouveau composé et diode électroluminescente organique le comprenant
WO2021166553A1 (fr) * 2020-02-17 2021-08-26 出光興産株式会社 Élément électroluminescent organique et appareil électronique
WO2021166552A1 (fr) * 2020-02-17 2021-08-26 出光興産株式会社 Élément électroluminescent organique et dispositif électronique
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CN115551853A (zh) * 2020-08-04 2022-12-30 株式会社Lg化学 新型化合物及包含其的有机发光器件

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