WO2020022771A1 - 유기 발광 소자 - Google Patents

유기 발광 소자 Download PDF

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WO2020022771A1
WO2020022771A1 PCT/KR2019/009168 KR2019009168W WO2020022771A1 WO 2020022771 A1 WO2020022771 A1 WO 2020022771A1 KR 2019009168 W KR2019009168 W KR 2019009168W WO 2020022771 A1 WO2020022771 A1 WO 2020022771A1
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group
light emitting
substituted
unsubstituted
formula
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PCT/KR2019/009168
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English (en)
French (fr)
Korean (ko)
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허정오
윤희경
허동욱
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주식회사 엘지화학
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Priority to CN201980032131.9A priority Critical patent/CN112119513B/zh
Publication of WO2020022771A1 publication Critical patent/WO2020022771A1/ko

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    • 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
    • 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
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • 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
    • 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
    • H10K50/12—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
    • 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
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6574—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes
    • 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]
    • H10K50/17—Carrier injection layers
    • H10K50/171—Electron injection layers
    • 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]
    • H10K50/18—Carrier blocking layers

Definitions

  • the present specification relates to an organic light emitting device.
  • organic light emitting phenomenon refers to a phenomenon of converting electrical energy into light energy using an organic material.
  • An organic light emitting device using an organic light emitting phenomenon usually has a structure including an anode, a cathode and an organic material layer therebetween.
  • the organic material layer is formed of a multi-layered structure composed of different materials in order to increase the efficiency and stability of the organic light emitting device.
  • the present specification provides an organic light emitting device.
  • One embodiment of the present specification is a cathode; An anode provided opposite the cathode;
  • a light emitting layer provided between the cathode and the anode; A first organic material layer provided between the cathode and the light emitting layer and including a compound represented by Chemical Formula 1 below; And a second organic material layer provided between the cathode and the first organic material layer and including the compound represented by the following Chemical Formula 2.
  • X is O or S
  • At least one of R 1 to R 16 is a group represented by the following formula (A), and the others are the same as or different from each other, and each independently hydrogen; Alkyl groups; Or an aryl group unsubstituted or substituted with an alkyl group, or combine with an adjacent group to form an aromatic hydrocarbon ring,
  • At least one of X1 to X3 is N, and the others are CR ';
  • R ' is hydrogen or combines with-(L2) l2 -Ar2 or-(L3) l3 -Ar3 to form an aromatic hydrocarbon ring substituted or unsubstituted with a heterocyclic ring,
  • L1 to L3 are the same as or different from each other, and each independently a direct bond; An arylene group unsubstituted or substituted with an alkyl group, an aryl group, or a heterocyclic group; Or a divalent heterocyclic group unsubstituted or substituted with one or more substituents selected from the group consisting of an alkyl group, an aryl group, a heterocyclic group, and an aryl group substituted with an alkyl group,
  • Ar2 and Ar3 are the same as or different from each other, and each independently an aryl group unsubstituted or substituted with an alkyl group, haloalkyl group, haloalkoxy group, or heteroaryl group; An silyl group unsubstituted or substituted with an alkyl group or an aryl group; Or a heterocyclic group unsubstituted or substituted with an alkyl group or an aryl group,
  • l1 to l3 are each independently an integer of 1 to 3,
  • L1 When l1 is 2 or more, two or more L1 are the same as or different from each other,
  • L2 When l2 is 2 or more, two or more L2s are the same as or different from each other,
  • L3 When l3 is 2 or more, two or more L3 are the same as or different from each other,
  • At least one of Y1 to Y3 is N, and the other is CH;
  • G1 and G2 are the same as or different from each other, and each independently an aryl group unsubstituted or substituted with an aryl group,
  • L11 and L12 are the same as or different from each other, and each independently a substituted or unsubstituted divalent to tetravalent aromatic hydrocarbon ring group; Or a substituted or unsubstituted divalent to tetravalent heterocyclic group,
  • G11 is a direct bond; O; Substituted or unsubstituted arylene group; Or a substituted or unsubstituted divalent heterocyclic group,
  • a to d are each independently an integer of 1 to 3,
  • the organic light emitting diode according to the exemplary embodiment of the present specification may improve the injection ability of electrons coming from the cathode, thereby providing a low driving voltage and a high luminous efficiency.
  • 1 to 5 illustrate examples of the organic light emitting device according to the exemplary embodiment of the present specification.
  • One embodiment of the present specification is a cathode; An anode provided opposite the cathode;
  • a light emitting layer provided between the cathode and the anode; A first organic material layer provided between the cathode and the light emitting layer and including the compound represented by Chemical Formula 1; And a second organic material layer provided between the cathode and the first organic material layer and including the compound represented by Chemical Formula 2.
  • the compound of Formula 1 is used in the hole blocking layer in a non-linear structure, it is possible to improve the efficiency of the organic light emitting device, low driving voltage and lifetime characteristics.
  • at least one of R1 to R16 is Formula A, and since Formula A is an electron depletion structure, the polarity of the molecule can be designed to be nearly nonpolar. It is possible to form an amorphous layer in the fabrication of an organic light emitting device including the compound represented by 1 in the hole blocking layer. Therefore, the organic light emitting diode according to the exemplary embodiment of the present specification may improve efficiency, lower driving voltage, and lifespan characteristics.
  • the compound represented by Formula 1 has a three-dimensional horizontal structure, the electron mobility is enhanced when the organic material layer is formed of such a material.
  • energy level means the energy size. Therefore, the energy level is interpreted to mean the absolute value of the energy value. For example, a low or deep energy level means that the absolute value increases in the negative direction from the vacuum level.
  • HOMO highest occupied molecular orbital
  • LUMO lowest unoccupied molecular orbital
  • the HOMO energy level means the distance from the vacuum level to the HOMO.
  • LUMO energy level means the distance from a vacuum level to LUMO.
  • the bandgap means a difference in energy level between HOMO and LUMO, that is, HOMO-LUMO gap (Gap).
  • the compound represented by Chemical Formula 1 may have a HOMO energy level of 6.0 eV or more, a triplet energy level of 2.5 eV or more, and a bandgap of 3.0 eV or more. Can be.
  • the triplet energy of the light emitting layer is not transferred to the adjacent layer, thereby increasing the efficiency of the organic light emitting device.
  • the HOMO energy level in the hole blocking layer has a value of 6.0 eV or more, it prevents hole transfer from the light emitting layer, thereby making it possible to make a high efficiency and long life device.
  • the electron mobility is high and the driving voltage is low when the organic light emitting device is used, and high efficiency and long life are exhibited.
  • the LUMO energy level has a value of 3.0 eV to 2.6 eV, the energy barrier with the light emitting layer is not large, which facilitates electron injection.
  • the LUMO energy level refers to an energy level in a region having a low energy barrier with the light emitting layer.
  • the HOMO energy level may be measured using an atmospheric photoelectron spectrometer (manufactured by RIKEN KEIKI Co., Ltd .: AC3), and the LUMO energy level may be calculated as a wavelength value measured through photoluminescence (PL). Can be.
  • the compound represented by Chemical Formula 2 is a structure in which CN is bonded through a 6-membered heterocyclic ring containing N and linking groups L11, G11, and L12, and has a suitable twisting structure, so that the conjugate between substituents Conjugation, which maintains the independent characteristics of the substituents and is appropriately maintained at the same time as the electronic interaction due to the gate is small, is a structural feature that prevents the lifespan of the organic light emitting device due to excessive electron injection. Improvement, low driving voltage and life characteristics can be improved.
  • the first organic material layer is a hole blocking layer.
  • the second organic silver layer is an electron transport layer, an electron injection layer, or an electron injection and transport layer.
  • the second organic material is a layer electron injection layer.
  • the second organic material is a layer electron transport layer.
  • the second organic material is a layer electron injection and transport layer.
  • the first organic material layer is a hole blocking layer, and the hole blocking layer is provided in contact with the light emitting layer.
  • the first organic material layer is a hole blocking layer
  • the second organic material is a layer electron transport layer, an electron injection layer, or an electron injection and transport layer
  • the hole blocking layer is provided in contact with the light emitting layer.
  • the first organic material layer includes the compound represented by Formula 1 and the second organic material layer includes the compound represented by Formula 2, Formula 1 having excellent hole blocking ability.
  • the formula (2) excellent in the electron injection and transport ability is applied to the organic light emitting device at the same time, by controlling the material contained in the electron blocking layer and the electron transport layer (or electron injection and transport layer), by adjusting the energy level between each layer Driving voltage, efficiency and / or life characteristics can be improved.
  • Chemical Formula 1 of the first organic compound layer does not include CN
  • Chemical Formula 2 of the second organic compound layer necessarily includes CN, and due to structural differences between the compounds included in the first organic layer and the second organic compound layer, The dipole moment and LUMO energy level between the first organic material layer and the second organic material layer are adjusted, and the amount of electrons transported to the light emitting layer is controlled to prevent excessive amounts of electrons from being injected into the light emitting layer at the same time, thereby improving the life of the organic light emitting device. It is effective.
  • the compound represented by Formula 1 and the compound represented by Formula 2 satisfy the following Formula 1.
  • the dipole moment is a physical quantity indicating the degree of polarity and may be calculated by Equation 1 below.
  • the value of the dipole moment can be obtained.
  • the molecular density can be obtained by calculating charges and dipoles for each atom using a method called Hirshfeld Charge Analysis, and calculating them according to the following equation. Obtain Dipole Moment.
  • the shape of the entire molecule of Formula 2 does not significantly affect the shape of the molecule, and includes a cyano group that can greatly increase the dipole moment, and the structure of Formula 1 does not include a cyano group.
  • the dipole moment is greatly increased in Chemical Formula 2 including the cyano group
  • the second organic material layer including the same and the first organic layer including Chemical Formula 1 not including the cyano group satisfy Formula 1, and the dipole moment.
  • LUMO energy levels show a great difference, which acts as a barrier between the first organic material layer in the second organic material layer, thereby controlling the amount and rate of electrons injected from the cathode to the light emitting layer, thereby improving the life of the organic light emitting device.
  • substituted means that a hydrogen atom bonded to a carbon atom of the compound is replaced with another substituent, and the position to be substituted is not limited to a position where the hydrogen atom is substituted, that is, a position where a substituent can be substituted, if two or more substituted , Two or more substituents may be the same or different from each other.
  • the term "substituted or unsubstituted” is deuterium; Halogen group; Hydroxyl group; Cyano group; Alkyl groups; Cycloalkyl group; Alkenyl groups; An alkoxy group; Aryloxy group; Silyl groups; Haloalkyl group; Haloalkoxy group; Aryl group; And it is substituted with one or more substituents selected from the group consisting of a heterocyclic group, or two or more substituents of the substituents exemplified above are substituted, or means that do not have any 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 or may be interpreted as a substituent to which two phenyl groups are linked.
  • examples of the halogen group include fluorine, chlorine, bromine or iodine.
  • the alkyl group may be straight or branched chain, carbon number is not particularly limited, but is preferably 1 to 30.
  • Specific examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n-pentyl Isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl, n-heptyl, 1-methylhexyl, Cyclopentylmethyl, cyclohexylmethyl, octyl, n-octyl, tert-oct
  • the cycloalkyl group is not particularly limited, but preferably 3 to 30 carbon atoms, specifically, cyclopropyl, cyclobutyl, cyclopentyl, 3-methylcyclopentyl, 2,3-dimethylcyclopentyl, cyclohexyl, 3-methylcyclohexyl, 4-methylcyclohexyl, 2,3-dimethylcyclohexyl, 3,4,5-trimethylcyclohexyl, 4-tert-butylcyclohexyl, cycloheptyl, cyclooctyl, and the like, but are not limited thereto. It is not.
  • the alkenyl group may be linear or branched chain, the carbon number is not particularly limited, but is preferably 2 to 30.
  • 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 alkoxy group may be linear, branched or cyclic. Although carbon number of an alkoxy group is not specifically limited, It is preferable that it is C1-C30. Specifically, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, tert-butoxy, sec-butoxy, n-pentyloxy, neopentyloxy, isopentyloxy, n -Hexyloxy, 3,3-dimethylbutyloxy, 2-ethylbutyloxy, n-octyloxy, n-nonyloxy, n-decyloxy, benzyloxy, p-methylbenzyloxy, and the like, but It is not limited.
  • the aryl group is not particularly limited, but preferably has 6 to 30 carbon atoms, and the aryl group may be monocyclic or polycyclic.
  • the aryl group is a monocyclic aryl group
  • carbon number is not particularly limited, but is preferably 6 to 30 carbon atoms.
  • the monocyclic aryl group may be a phenyl group, a biphenyl group, a terphenyl group, etc., but is not limited thereto.
  • Carbon number is not particularly limited when the aryl group is a polycyclic aryl group. It is preferable that it is C10-30.
  • the polycyclic aryl group may be a naphthyl group, anthracene group, phenanthrenyl group, triphenylenyl group, pyrenyl group, penalenyl group, perrylenyl group, chrysenyl group, fluorenyl group, etc., but is not limited thereto. It is not.
  • the fluorenyl group may be substituted, and adjacent groups may combine with each other to form a ring.
  • the fluorenyl group When the fluorenyl group is substituted, it may have a structure as follows, but is not limited thereto.
  • adjacent means a substituent substituted on an atom directly connected to the atom to which the corresponding substituent is substituted, a substituent positioned closest to the substituent, or another substituent substituted on the atom to which the substituent is substituted.
  • two substituents substituted at the ortho position in the benzene ring and two substituents substituted at the same carbon in the aliphatic ring may be interpreted as "adjacent" groups.
  • the heterocyclic group includes one or more atoms other than carbon and hetero atoms, and specifically, the hetero atoms may include one or more atoms selected from the group consisting of O, N, Se, and S. Although carbon number is not particularly limited, it is preferably 2 to 30 carbon atoms, the heteroaryl group may be monocyclic or polycyclic.
  • heterocyclic group examples include a thiophenyl group, furanyl group, pyrrolyl group, imidazolyl group, thiazolyl group, oxazolyl group, oxadiazolyl group, pyridinyl group, bipyridinyl group, pyrimidinyl group, triazinyl group, Triazolyl, acridinyl, pyridazinyl, pyrazinyl, quinolinyl, quinazolinyl, quinoxalinyl, phthalazinyl, pyrido pyrimidinyl, pyrido pyrazinyl, pyrazinopyrazinyl Group, pyrido indolyl group, isoquinolinyl group, indolyl group, carbazolyl group, benzoxazolyl group, benzimidazolyl group, benzothiazolyl group, benzocarbazolyl group, benzothi
  • the aryl group in the aryloxy group is the same as the example of the aryl group described above. Specifically, as the aryloxy group, phenoxy group, p-tolyloxy group, m- toryloxy group, 3,5-dimethyl-phenoxy group, 2,4,6-trimethylphenoxy group, p-tert-butylphenoxy group, 3- Biphenyloxy group, 4-biphenyloxy group, 1-naphthyloxy group, 2-naphthyloxy group, 4-methyl-1-naphthyloxy group, 5-methyl-2-naphthyloxy group, 1-anthracenyloxy group , 2-anthracenyloxy group, 9-anthracenyloxy group, 1-phenanthrenyloxy group, 3-phenanthrenyloxy group, 9-phenanthrenyloxy group, and the like, but are 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 haloalkyl group means that a halogen group is substituted for hydrogen of the alkyl group, and examples of the alkyl group may be applied except that H is a halogen group in the alkyl group.
  • H is a halogen group in the alkyl group.
  • -CF 3 -CHF 2 , -CH 2 F and the like, but is not limited thereto.
  • the haloalkoxy group means that a halogen group is substituted for hydrogen of the alkoxy group, and examples of the alkoxy group may be applied except that H is a halogen group in the alkoxy group.
  • H is a halogen group in the alkoxy group.
  • -OCF 3, -OCHF 2, -OCH 2 F, etc. but is not limited thereto.
  • the arylene group refers to a divalent group having two bonding positions in the aryl group.
  • the description of the aforementioned aryl groups can be applied except that they are each divalent.
  • the divalent heterocyclic group refers to a divalent group having two bonding positions in the heterocyclic group.
  • the description of the aforementioned heterocyclic groups can be applied except that they are each divalent.
  • a “ring” in a substituted or unsubstituted ring in which adjacent groups are bonded to each other, a “ring” means a substituted or unsubstituted aromatic hydrocarbon ring; Or a substituted or unsubstituted hetero ring.
  • the aromatic hydrocarbon ring may be monocyclic or polycyclic, and may be selected from examples of the cycloalkyl group or aryl group except that they are not monovalent.
  • the heterocycle includes one or more atoms other than carbon and heteroatoms, and specifically, the heteroatoms may include one or more atoms selected from the group consisting of O, N, Se, and S.
  • the heterocycle may be monocyclic or polycyclic, may be aromatic, aliphatic or a condensed ring of aromatic and aliphatic, and may be selected from examples of the heterocyclic group except that it is not monovalent.
  • the divalent to tetravalent aromatic hydrocarbon ring group may be monocyclic or polycyclic, meaning that the aryl group has 2 to 4 bonding positions, that is, 2 to 4 valent groups.
  • the description of the aforementioned aryl groups can be applied except that they are each divalent to tetravalent.
  • the divalent to tetravalent heterocyclic group may be monocyclic or polycyclic, meaning that the heterocyclic group has 2 to 4 bonding positions, that is, 2 to tetravalent groups.
  • the description of the aforementioned heterocyclic group may be applied except that they are each divalent to tetravalent.
  • X is O.
  • X is S.
  • Formula 1 is represented by the following formula 1-1 or 1-2.
  • L1 to L3, l1 to l3, Ar2, Ar3 and X1 to X3 are the same as those defined in Chemical Formula A,
  • At least one of X4 to X6 is N, and the others are CR ';
  • R ' is hydrogen or combines with-(L5) l5 -Ar4 or-(L6) l6 -Ar5 to form an aromatic hydrocarbon ring substituted or unsubstituted with a heterocyclic ring,
  • L4 to L6 are the same as or different from each other, and each independently a direct bond; An arylene group unsubstituted or substituted with an alkyl group, an aryl group, or a heterocyclic group; Or a divalent heterocyclic group unsubstituted or substituted with one or more substituents selected from the group consisting of an alkyl group, an aryl group, a heterocyclic group, and an aryl group substituted with an alkyl group,
  • Ar4 and Ar5 are the same as or different from each other, and each independently an aryl group unsubstituted or substituted with an alkyl group, haloalkyl group, haloalkoxy group, or heteroaryl group; An silyl group unsubstituted or substituted with an alkyl group or an aryl group; Or a heterocyclic group unsubstituted or substituted with an alkyl group or an aryl group,
  • l4 to l6 are each independently an integer of 1 to 3,
  • L4 is 2 or more
  • two or more L4s are the same as or different from each other
  • L5 When l5 is 2 or more, two or more L5s are the same as or different from each other,
  • L6 When l6 is 2 or more, two or more L6 are the same as or different from each other,
  • n1 is an integer of 0 to 2
  • n2 is an integer of 0 to 2
  • R100 and R101 are the same as or different from each other, and each independently hydrogen; Alkyl groups; Or an aryl group unsubstituted or substituted with an alkyl group, or combine with an adjacent group to form an aromatic hydrocarbon ring,
  • r100 and r101 are each independently an integer of 1 to 8,
  • R101 When r101 is two or more, two or more R101 are the same as or different from each other.
  • At least one of R1 to R16 is a group represented by the formula A, the rest are the same as or different from each other, and each independently hydrogen; Alkyl groups; A phenyl group unsubstituted or substituted with an alkyl group; Biphenyl group; Terphenyl group; Naphthyl group; Triphenylenyl group; Or a fluorenyl group unsubstituted or substituted with an alkyl group, or combine with an adjacent group to form a benzene ring.
  • At least one of R1 to R16 is a group represented by the formula A, the rest are the same as or different from each other, and each independently hydrogen; Methyl group; n-butyl group; t-butyl group; A phenyl group unsubstituted or substituted with a methyl group or a t-butyl group; Biphenyl group; Terphenyl group; Naphthyl group; Triphenylenyl group; Or fluorenyl unsubstituted or substituted with a methyl group, or combine with an adjacent group to form a benzene ring.
  • R1 to R16 are the same as or different from each other, and each independently represent a group represented by Formula A, and 0 to 3 of R1 to R16 are an alkyl group; Aryl group; Or an alkylaryl group, with the remainder being hydrogen.
  • At least one of the R1 to R16 is a group represented by the formula A, the remaining are the same as or different from each other, and each independently hydrogen; Alkyl groups; Aryl group; Or an arylalkyl group, or combine with adjacent groups to form a substituted or unsubstituted aromatic hydrocarbon ring.
  • the groups other than the group represented by the formula A in the R1 to R16, or combine with adjacent groups to form a substituted or unsubstituted aromatic hydrocarbon ring are the same as or different from each other, each independently t- Butylphenyl group; Methyl group; t-butyl group; Phenyl group; Methylphenyl group; n-butyl group; Naphthyl group; Triphenylenyl group; Or 9,9-dimethylfluorenyl group.
  • the groups capable of combining with adjacent groups of the R1 to R16 to form an aromatic hydrocarbon ring are R1 and R2, or R15 and R16. That is, according to the exemplary embodiment of the present specification, in Chemical Formula 1, at least one of R1 to R16 is a group represented by Chemical Formula A, and the others are the same as or different from each other, and each independently hydrogen; Alkyl groups; Or an aryl group unsubstituted or substituted with an alkyl group, R1 and R2 combine with each other to form an aromatic hydrocarbon ring, or R15 and R16 combine with each other to form an aromatic hydrocarbon ring.
  • the aromatic hydrocarbon ring formed by bonding R1 and R2 to each other may be a benzene ring
  • the aromatic hydrocarbon ring formed by bonding R15 and R16 to each other may be a benzene ring.
  • R1 and R2 are bonded to each other to form an aromatic hydrocarbon ring.
  • R1 and R2 are bonded to each other to form a benzene ring.
  • R15 and R16 are combined with each other to form an aromatic hydrocarbon ring.
  • R15 and R16 are combined with each other to form a benzene ring.
  • L1 to L3 are the same as or different from each other, and each independently a direct bond; A phenyl group unsubstituted or substituted with an alkyl group, an aryl group or a heterocyclic group; A biphenylene group unsubstituted or substituted with a heterocyclic group; Naphthylene group; Divalent fluorenyl group unsubstituted or substituted with an alkyl group; Divalent terphenyl group; Divalent pyridinyl group unsubstituted or substituted with a heterocyclic group; Divalent furanyl group; Divalent thiophenyl group; Divalent dibenzofuranyl group; Divalent dibenzothiophenyl group; A divalent carbazolyl group unsubstituted or substituted with an aryl group or an aryl group substituted with an alkyl group; A divalent dihydroindenocarbazolyl
  • L1 to L3 are the same as or different from each other, and each independently a direct bond;
  • L1 is a direct bond; An phenyl group unsubstituted or substituted with an alkyl group or an aryl group; Biphenylene group; Naphthylene group; Divalent fluorenyl group unsubstituted or substituted with an alkyl group; Divalent pyridinyl group; Divalent furanyl group; Divalent thiophenyl group; Divalent dibenzofuranyl group; Divalent dibenzothiophenyl group; A divalent carbazolyl group unsubstituted or substituted with an aryl group or an aryl group substituted with an alkyl group; Divalent dihydroindenocarbazolyl group unsubstituted or substituted with an alkyl group; A divalent benzocarbazolyl group unsubstituted or substituted with an aryl group substituted with an aryl group or an alkyl group; Divalent dibenzosil
  • L1 is a direct bond; A phenyl group unsubstituted or substituted with a methyl group or a phenyl group; Biphenylene group; Naphthylene group; Divalent fluorenyl group unsubstituted or substituted with a methyl group; Divalent pyridinyl group; Divalent furanyl group; Divalent thiophenyl group; Divalent dibenzofuranyl group; Divalent dibenzothiophenyl group; A divalent carbazolyl group unsubstituted or substituted with a phenyl group or a phenyl group substituted with a methyl group; Divalent dihydroindenocarbazolyl group unsubstituted or substituted with a methyl group; Divalent benzocarbazolyl group unsubstituted or substituted with a phenyl group or a biphenyl group substituted with a methyl
  • L2 and L3 are the same as or different from each other, and each independently a direct bond; A phenyl group unsubstituted or substituted with an alkyl group, an aryl group or a heterocyclic group; A biphenylene group unsubstituted or substituted with a heterocyclic group; Divalent terphenyl group; Divalent pyridinyl group unsubstituted or substituted with a heterocyclic group; Divalent dibenzofuranyl group; Divalent dibenzothiophenyl group; Divalent carbazolyl group unsubstituted or substituted with an aryl group; A divalent dihydroindenocarbazolyl group unsubstituted or substituted with one or more substituents selected from the group consisting of an alkyl group and an aryl group; Or a divalent phenazinyl group.
  • L2 and L3 are the same as or different from each other, and each independently a direct bond;
  • a divalent dihydroindenocarbazolyl group unsubstituted or substituted with one or more substituents selected from the
  • l1 is 1.
  • l1 is 2.
  • l1 is 3.
  • l2 is 1.
  • l2 is 2.
  • l2 is 3.
  • l3 is 1.
  • l3 is 2.
  • l3 is 3.
  • L1 is a divalent carbazolyl group; Or a phenylene group and l1 is 2,
  • the connection structure is not limited thereto.
  • L1 is a divalent carbazolyl group; Or a phenylene group and l1 is 3,
  • the connection structure is not limited thereto.
  • At least one of X1 to X3 is N, the remainder is CR.
  • X1 is N
  • X2 and X3 is CR.
  • X2 is N
  • X1 and X3 is CR.
  • X3 is N, X1 and X2 are CR.
  • X1 and X2 are N, X3 is CR.
  • X1 and X3 are N, X2 is CR.
  • X2 and X3 are N, X1 is CR.
  • X1 to X3 is N.
  • R is hydrogen
  • or-(L2) l2 -Ar2 or-(L3) l3 -Ar3 combines to form a benzene ring unsubstituted or substituted with a heterocyclic group.
  • R is hydrogen, or-(L2) l2 -Ar2 or-(L3) l3 -Ar3 is combined to form a benzene ring unsubstituted or substituted with a benzocarbazolyl group.
  • Ar2 and Ar3 are the same as or different from each other, and each independently an alkyl group or a silyl group unsubstituted or substituted with an aryl group; A phenyl group unsubstituted or substituted with an alkyl group or a haloalkyl group; A biphenyl group unsubstituted or substituted with a haloalkyl group; Naphthyl group; Terphenyl groups unsubstituted or substituted with a haloalkyl group, a haloalkoxy group, or a heterocyclic group; A fluorenyl group unsubstituted or substituted with an alkyl group; Phenanthrenyl group; Triphenylenyl group; Fluoranthenyl group; Phenenyl group; Pyridinyl group; Dibenzofuranyl group unsubstituted or substituted with an alkyl group
  • Ar2 and Ar3 are the same as or different from each other, and each independently a silyl group unsubstituted or substituted with a methyl group or a phenyl group; A methyl group or a phenyl group unsubstituted or substituted with -CF 3 ; A biphenyl group unsubstituted or substituted with -CF 3 ; Naphthyl group; Terphenyl group unsubstituted or substituted with a -CF 3 , -OCF 3 , or a pyridinyl group; A fluorenyl group unsubstituted or substituted with a methyl group; Phenanthrenyl group; Triphenylenyl group; Fluoranthenyl group; Phenenyl group; Pyridinyl group; Dibenzofuranyl group unsubstituted or substituted with a methyl group; Dibenzothiophen
  • Formula A is represented by any one of the following formula A-1 to A-3.
  • L1 and l1 are as defined in Formula A,
  • X11 is N or CH
  • X12 is N or CH
  • X13 is N or CH
  • at least two of X11 to X13 are N
  • Ar21 to Ar24 are the same as or different from each other, and each independently a substituent selected from the group consisting of a cyano group, a halogen group, an alkyl group, an alkoxy group, an aryl group, a trialkylsilyl group, a triarylsilyl group, and a heterocyclic group
  • a substituent selected from the group consisting of a cyano group, a halogen group, an alkyl group, an alkoxy group, an aryl group, a trialkylsilyl group, a triarylsilyl group, and a heterocyclic group
  • a heterocyclic group unsubstituted or substituted with one
  • R50 and R51 are the same as or different from each other, and each independently hydrogen; Alkyl groups; Aryl group; Or a heteroaryl group,
  • a50 is an integer of 0 to 4, when a50 is 2 or more, R50 is the same as or different from each other,
  • a51 is an integer of 0 to 4, and when a51 is 2 or more, R51 is the same as or different from each other.
  • the L1 is a direct bond; An arylene group unsubstituted or substituted with an alkyl group, an aryl group or a heterocyclic group; Or a divalent heterocyclic group unsubstituted or substituted with an alkyl group, an alkylaryl group or an aryl group.
  • the L1 is a direct bond; A C6-18 arylene group unsubstituted or substituted with a C1-6 alkyl group, a C6-20 aryl group, or a C2-20 heteroaryl group; Or a divalent C2-20 heterocyclic group unsubstituted or substituted with a C1-6 alkyl group, a C6-20 alkylaryl group, or a C6-20 aryl group.
  • the L1 is a direct bond; C6-13 arylene group unsubstituted or substituted with a C1-6 alkyl group, C6-12 aryl group, or C2-12 heteroaryl group; Or a divalent C2-16 heterocyclic group unsubstituted or substituted with a C1-6 alkyl group, a C6-16 alkylaryl group, or a C6-15 aryl group.
  • the L1 is a direct bond; A phenylene group unsubstituted or substituted with a methyl group or a phenyl group; Biphenylene group; Divalent naphthyl group; Divalent furanyl group; Divalent thiophenyl group; Divalent pyridinyl group; Divalent dibenzofuranyl group; Divalent dibenzothiophenyl group; A divalent carbazolyl group unsubstituted or substituted with a methylphenyl group or a phenyl group; A biphenyl group substituted with a methyl group or a divalent benzocarbazolyl group unsubstituted or substituted with a phenyl group; Divalent indenocarbazolyl group unsubstituted or substituted with a methyl group; Divalent dibenzosilolyl group unsubstituted or substituted with a methyl group; ; ; Or
  • Ar21 to Ar24 are the same as or different from each other, and each independently a trialkylsilyl group; Triarylsilyl group; Group consisting of cyano group, haloalkyl group, haloalkoxy group, trialkylsilyl group, triarylsilyl group, alkyl group, aryl group and heterocyclic group unsubstituted or substituted with 'alkyl group, alkylaryl group, aryl group or heterocyclic group' An aryl group unsubstituted or substituted with one or more substituents selected from; Or a heterocyclic group unsubstituted or substituted with one or more substituents selected from the group consisting of an alkyl group, a heteroarylaryl group, an aryl group and a heterocyclic group.
  • Ar21 to Ar24 are the same as or different from each other, and each independently triphenylsilyl group; Dibenzofuranyl group unsubstituted or substituted with a trifluoromethyl group, trifluoromethoxy group, trimethylsilyl group, methyl group, biphenyl group, triphenylenyl group, fluoranthenyl group, 'methyl group, phenyl group or dibenzofuranyl group' Pyridyl unsubstituted or substituted with carbazolyl, benzocarbazolyl, phenyl or pyridinyl groups unsubstituted or substituted with a dibenzothiophenyl group, carbazolyl group, a methyl group, a phenyl group, a biphenyl group or a triphenylenyl group A phenyl group unsubstituted or substituted with an indenocarbazolyl group, a dimethyld
  • the R50 and R51 are the same as or different from each other, and each independently a heteroaryl group.
  • the R50 and R51 are the same as or different from each other, and each independently a benzocarbazolyl group.
  • the compound represented by Formula 1 is selected from the following compounds.
  • a is 2.
  • a is 3.
  • Chemical Formula 2 is represented by any one of the following Chemical Formulas 2-1 to 2-3.
  • At least one of Y4 to Y9 is N, and the others are CH;
  • G3 to G6 are the same as or different from each other, and are each independently an aryl group unsubstituted or substituted with an aryl group.
  • Y1 is N
  • Y2 and Y3 are CH.
  • Y2 is N
  • Y1 and Y3 is CH.
  • Y3 is N
  • Y1 and Y2 are CH.
  • Y1 and Y2 are N, Y3 is CH.
  • Y1 and Y3 are N, Y2 is CH.
  • Y2 and Y3 are N, Y1 is CH.
  • Y1 to Y3 is N.
  • G1 and G2 are the same as or different from each other, and each independently a phenyl group; Biphenyl group; Or a fluorenyl group unsubstituted or substituted with an aryl group.
  • G1 and G2 are the same as or different from each other, and each independently a phenyl group; Biphenyl group; Or a fluorenyl group unsubstituted or substituted with a phenyl group.
  • G1 and G2 are the same as or different from each other, and each independently a phenyl group; Biphenyl group; Or 9,9-diphenyl-9H-fluorenyl group.
  • L11 and L12 are the same as or different from each other, and each independently an aryl group, heterocyclic ring substituted with a cyano group, an aryl group, a heterocyclic group, a cyano group and an alkyl group
  • L11 and L12 are the same as or different from each other, and each independently an aryl group, heterocyclic ring substituted with a cyano group, an aryl group, a heterocyclic group, a cyano group and an alkyl group
  • An aryl group substituted with a group or a 2 to tetravalent phenyl group unsubstituted or substituted with an aryl group substituted with a cyano group A divalent to tetravalent biphenyl group unsubstituted or substituted with an aryl group substituted with a cyano group; 2-4 tetravalent naphthyl group; A divalent to tetravalent terphenyl group unsubstituted or substituted with an aryl group substituted with a cyano group; Divalent to tetravalent fluorenyl group unsubstituted or substituted with an alkyl group; Or a
  • L11 and L12 are the same as or different from each other, and each independently substituted with a cyano group, a biphenyl group, a phenanthrenyl group, a dibenzothiophenyl group, a xanthenyl group, a phenyl group A fluorenyl group substituted with a substituted fluorenyl group, a cyano group and a methyl group, a phenyl group substituted with a pyridinyl group, or a 2 to tetravalent phenyl group unsubstituted or substituted with a phenyl group substituted with a cyano group; Divalent to tetravalent biphenyl group unsubstituted or substituted with a fanyl group substituted with a cyano group; 2-4 tetravalent naphthyl group; A divalent to tetravalent terphenyl group;
  • L11 is a C6-C17 bivalent aromatic hydrocarbon ring group unsubstituted or substituted with R21; Or a C2-C30 divalent heterocyclic group unsubstituted or substituted with R21.
  • L11 is a C6-C13 divalent aromatic hydrocarbon ring group unsubstituted or substituted with R21; Or a C2-C25 divalent heterocyclic group unsubstituted or substituted with R21.
  • L11 is a C6-C13 bivalent aryl group unsubstituted or substituted with R21; Or a C2-C2 bivalent heterocyclic group which is unsubstituted or substituted with R21 and contains only O as a hetero atom.
  • L11 is a substituted or unsubstituted divalent or tetravalent phenyl group; A substituted or unsubstituted divalent to tetravalent naphthyl group; A substituted or unsubstituted divalent to tetravalent fluorenyl group; Or a substituted or unsubstituted divalent to tetravalent spiro [fluorene-9,9 '] xanthenyl group.
  • L11 is a bivalent to tetravalent phenyl group unsubstituted or substituted with R21; Divalent or tetravalent naphthyl groups; Divalent to tetravalent fluorenyl group unsubstituted or substituted with a methyl group or a phenyl group; Or a divalent to tetravalent spiro [fluorene-9,9'-xanthene] yl group.
  • R21 is an aryl group unsubstituted or substituted with a cyano group, an alkyl group, an aryl group or a heteroaryl group; Or a heterocyclic group.
  • R21 is an aryl group unsubstituted or substituted with a cyano group, an alkyl group, an aryl group, or an N-containing heteroaryl group; Or an O-containing heterocyclic group.
  • R21 is a 9,9-dimethyl-9H-fluorenyl group unsubstituted or substituted with a cyano group; Spiro [fluorene-9,9'-xanthene] yl group; Or a phenyl group substituted with a pyridinyl group.
  • L12 is a divalent aromatic hydrocarbon ring group unsubstituted or substituted with R22; Or a divalent heterocyclic group unsubstituted or substituted with R 23.
  • L12 is a divalent aromatic hydrocarbon ring group unsubstituted or substituted with R22; Or a divalent heterocyclic group.
  • L12 is a C6-C20 divalent aromatic hydrocarbon ring group unsubstituted or substituted with R22; Or a divalent heterocyclic group having 2 to 30 carbon atoms.
  • L12 is a C6-C15 divalent aromatic hydrocarbon ring group unsubstituted or substituted with R22; Or a divalent heterocyclic group having 2 to 25 carbon atoms.
  • R22 is an aryl group which is unsubstituted or substituted with a cyano group or a heteroaryl group; Or a heteroaryl group.
  • R22 is an aryl group which is unsubstituted or substituted with a cyano group or an N-containing heteroaryl group; Or a heteroaryl group containing O or S.
  • R22 is a cyano group or an aryl group which is unsubstituted or substituted with a heteroaryl group containing only N as a hetero atom; Or a heteroaryl group containing only O or S as a heteroatom.
  • R22 is a dibenzothiophenyl group; Phenanthrenyl group; Cyanophenyl group; Or a pyridinylphenyl group.
  • L12 is a substituted or unsubstituted phenylene group; A substituted or unsubstituted divalent fluorenyl group; A substituted or unsubstituted divalent naphthyl group; Or a substituted or unsubstituted divalent spiro [fluorene-9,9'-xanthene] yl group.
  • L12 is a phenylene group unsubstituted or substituted with a dibenzothiophenyl group, a phenanthrenyl group, a cyanophenyl group or a pyridinylphenyl group; Divalent 9,9-dimethyl-9H-fluorenyl group; Divalent 9,9-diphenyl-9H-fluorenyl group; Divalent naphthyl group; Or a divalent spiro [fluorene-9,9'-xanthene] yl group.
  • G11 is a direct bond; O; An arylene group unsubstituted or substituted with an aryl group unsubstituted or substituted with an alkyl group or a cyano group; Or a divalent heterocyclic group.
  • G11 is a direct bond; O; Phenylene group; Naphthylene group; Divalent fluorenyl group unsubstituted or substituted with an alkyl group, cyanoaryl group or aryl group; Divalent dibenzofuranyl group; Or a divalent spiro [fluorene-9,9'-xanthene] yl group.
  • G11 is a direct bond; O; Phenylene group; Naphthylene group; Divalent fluorenyl group unsubstituted or substituted with a methyl group, cyanophenyl group or phenyl group; Divalent dibenzofuranyl group; Or a divalent spiro [fluorene-9,9-xanthene] yl group.
  • the G11 is a direct bond; -O-; An arylene group unsubstituted or substituted with an alkyl group, an aryl group or a cyanoaryl group; Or O-containing heteroarylene group.
  • the G11 is a direct bond; A phenylene group unsubstituted or substituted with a cyanoaryl group; Divalent naphthyl group; Divalent fluorenyl group unsubstituted or substituted with an alkyl group or an aryl group; Divalent dibenzofuranyl group; -O-; Or a divalent spiro [fluorene-9,9'-xanthene] yl group.
  • the G11 is a direct bond; A phenylene group unsubstituted or substituted with a cyanophenyl group; Divalent naphthyl group; Divalent fluorenyl group unsubstituted or substituted with a methyl group or a phenyl group; Divalent dibenzofuranyl group; -O-; Or a divalent spiro [fluorene-9,9'-xanthene] yl group.
  • b is 1 or 2.
  • d is 1.
  • d is 2.
  • d is 3.
  • the G11 when d is 2 or more, the G11 is connected in series.
  • G11 may be a phenylene group; Or a naphthylene group and d is 2,
  • the connection structure is not limited thereto.
  • the compound represented by Formula 2 is selected from the following compounds.
  • the light emitting layer includes a host and a dopant, and the maximum emission wavelength of the dopant is in a range of 420 nm to 520 nm.
  • the dopant is a blue fluorescent dopant.
  • the organic light emitting device includes a first organic material layer including a compound represented by Chemical Formula 1 between a cathode and a light emitting layer, and a second compound including the compound represented by Chemical Formula 2 between the cathode and the first organic material layer.
  • An organic light emitting device including an organic material layer has a life improvement effect of an organic light emitting device that emits blue light as a blue organic light emitting device.
  • the host may include one or more materials.
  • the host includes at least one of the compounds represented by the formula 3-1 and 3-2.
  • the energy level of the organic material layer and the light emitting layer is appropriately made, and thus the amount of electrons moved from the organic material layer to the light emitting layer is easily controlled, thereby improving the lifespan of the organic light emitting device.
  • L31 to L35 are the same as or different from each other, and each independently a direct bond; Substituted or unsubstituted arylene group; Or a substituted or unsubstituted divalent heterocyclic group,
  • Ar31 to Ar35 are the same as or different from each other, and each independently a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heterocyclic group,
  • R200 and R201 are the same as or different from each other, and each independently hydrogen; Or a substituted or unsubstituted aryl group,
  • r200 is an integer from 1 to 8
  • r201 is an integer of 1 to 7
  • R200 When r200 is 2 or more, two or more R200 are the same as or different from each other,
  • R201 When r201 is 2 or more, two or more R201 are the same as or different from each other.
  • the L31 to L35 are the same as or different from each other, and each independently a direct bond; Or an arylene group.
  • the L31 to L35 are the same as or different from each other, and each independently a direct bond; Phenylene group; Naphthylene group; Or a divalent anthracenyl group.
  • Ar31 to Ar35 are the same as or different from each other, and each independently an aryl group unsubstituted or substituted with deuterium; Or a heterocyclic group which is unsubstituted or substituted with an aryl group.
  • Ar31 to Ar35 are the same as or different from each other, and each independently a phenyl group unsubstituted or substituted with deuterium; Biphenyl group; Naphthyl group; Thiophenyl group unsubstituted or substituted with a phenyl group; Dibenzofuranyl group; Dibenzothiophenyl group; Benzo [b] naphtho [1,2-d] furanyl group; Benzo [b] naphtho [2,3-d] furanyl group; Or a benzo [d] naphtho [1,2-b] furanyl group.
  • the R200 is hydrogen; Or an aryl group unsubstituted or substituted with an aryl group.
  • the R200 is hydrogen; Or a naphthyl group unsubstituted or substituted with a phenyl group.
  • the R201 is hydrogen
  • the host is any one or more selected from the following compounds.
  • the compounds of Formulas 1 and 2 may be prepared using starting materials and reaction conditions known in the art.
  • the type and number of substituents can be determined by those skilled in the art as appropriately selecting known starting materials.
  • the compounds of Formulas 1 and 2 may be obtained from commercially available.
  • the organic light emitting device may include two or more light emitting layers.
  • the two or more light emitting layers may be provided in contact with each other, or may include an additional organic material layer between the two light emitting layers.
  • the organic light emitting device includes two or more light emitting layers, and includes a charge generating layer between two adjacent light emitting layers among the two or more light emitting layers, and the charge generating layer includes an n-type organic compound layer and p. It may include a type organic compound layer.
  • the n-type organic compound layer and the p-type organic compound layer included in the charge generating layer are NP bonded.
  • the p-type organic compound layer is selected from the group consisting of a hole injection layer, a hole transport layer, an electron blocking layer and a light emitting layer
  • the n-type organic compound layer is an electron transport layer, an electron injection layer, a hole blocking layer and a light emitting layer It is selected from the group consisting of.
  • n-type means n-type semiconductor characteristics.
  • n-type is a property that electrons are injected or transported through a lower unoccupied molecular orbital (LUMO) energy level, which can be defined as a property of a material in which electron mobility is greater than hole mobility.
  • p-type means p-type semiconductor characteristics.
  • p-type is a property of injecting or transporting holes through a high occupied molecular orbital (HOMO) energy level, which may be defined as a property of a material in which the hole mobility is greater than the electron mobility.
  • the compound or organic compound layer having n-type characteristics may be referred to as an n-type compound or n-type organic compound layer.
  • the compound or organic compound layer having a p-type characteristic may be referred to as a p-type compound or p-type organic compound layer.
  • n-type doping may mean that it is doped to have n-type characteristics.
  • the charge generating layer is a layer that generates charge without applying an external voltage, and generates two or more light emitting layers in the organic light emitting device by generating charges between adjacent light emitting layers among the light emitting layers. .
  • the NP junction may mean not only physical contact between the second electron transport layer, which is the n-type organic compound layer, and the p-type organic compound layer, but also an interaction in which holes and electrons may be easily generated and transported.
  • the NP junction when the NP junction is formed, it may be easy to form holes or electrons by an external voltage or a light source. Therefore, it is possible to prevent the rise of the driving voltage for the injection of holes.
  • the maximum light emission wavelength of at least two of the two or more light emitting layers is the same or different from each other.
  • the maximum emission wavelength means a wavelength at the maximum value of the spectral distribution.
  • the maximum light emission wavelength of at least two layers of the two or more light emitting layers are different from each other.
  • At least one of the two or more light emitting layers includes a phosphorescent dopant, and at least one includes a fluorescent dopant.
  • the blue fluorescence, green phosphorescence, and red phosphorescence stack including two or more light emitting layers different from each other;
  • a white light emitting device can be manufactured by stacking blue fluorescent light and green yellow phosphorescent light.
  • the organic light emitting diode according to the exemplary embodiment of the present specification may include a fluorescent layer and / or a phosphorescent layer.
  • the peak wavelength of the photoluminescence spectrum is 400 nm to 500 nm
  • the peak wavelength of the photoluminescence spectrum is 510 nm to 580 nm
  • the peak wavelength of the photoluminescence spectrum is 610 From nm to 680 nm, those skilled in the art can use one or two or more layers in combination with light emitting layers having different peak wavelengths as necessary.
  • the phosphorescent dopant and the fluorescent dopant may use a dopant generally used in the art.
  • the organic light emitting device includes a first light emitting layer provided between the anode and the first organic material layer; And a second light emitting layer provided on the first light emitting layer.
  • first light emitting layer and the second light emitting layer may be provided in contact with each other, and an additional organic material layer may be provided between the first light emitting layer and the second light emitting layer.
  • the organic light emitting diode includes: a first light emitting layer provided at a portion between the anode and the first organic material layer; And a second light emitting layer provided on the remaining part between the anode and the first organic material layer.
  • An insulating structure may be included between the first light emitting layer and the second light emitting layer.
  • the first emission layer and the second emission layer may be provided side by side on the same surface of the first organic material layer.
  • one side of the first light emitting layer and one side of the second light emitting layer may be provided in contact with each other.
  • the first light emitting layer and the second light emitting layer provided side by side may be provided in contact with the same surface of the first organic material layer.
  • an additional layer may be provided between the first light emitting layer and the second light emitting layer and the first organic material layer provided side by side.
  • the organic light emitting device includes a first light emitting layer provided between the anode and the first organic material layer; And a second light emitting layer provided on the first light emitting layer, and a third light emitting layer provided on the second light emitting layer.
  • the first light emitting layer, the second light emitting layer, and the third light emitting layer may be provided in contact with each other, and between the first light emitting layer and the second light emitting layer and / or between the second light emitting layer and the third light emitting layer. Additional organic layer may be provided.
  • the maximum light emission wavelengths of the first light emitting layer, the second light emitting layer, and the third light emitting layer are different from each other.
  • the maximum light emission wavelengths of the first light emitting layer, the second light emitting layer, and the third light emitting layer are the same.
  • the first emission layer, the second emission layer, and the third emission layer may include a blue fluorescent dopant, and the maximum emission wavelength of the dopant may be in a range of 420 nm to 520 nm.
  • the structure of the organic light emitting device according to the present invention may have a structure as shown in FIGS. 1 to 5, but is not limited thereto.
  • FIG. 1 illustrates an organic light emitting device in which an anode 201, a hole transport layer 301, a light emitting layer 401, a hole blocking layer 701, an electron transport layer 501, and a cathode 601 are sequentially stacked on a substrate 101.
  • the hole blocking layer 701 may be a first organic material layer
  • the electron transport layer 501 may be a second organic material layer.
  • a hole injection layer may be further provided between the anode 201 and the hole transport layer 301, and the hole injection layer may be further provided in FIG. 2.
  • FIG. 2 illustrates an organic light emitting device in which an anode 201, a hole transport layer 301, a light emitting layer 401, a hole blocking layer 701, an electron transport layer 501, and a cathode 601 are sequentially stacked on a substrate 101.
  • the hole blocking layer 701 may be a first organic material layer
  • the electron transport layer 501 may be a second organic material layer.
  • an anode 201, a hole injection layer 801, a hole transport layer 301, a light emitting layer 401, a hole blocking layer 701, an electron transport layer 501, and a cathode 601 are sequentially formed on the substrate 101.
  • the structure of the stacked organic light emitting device is illustrated.
  • the hole blocking layer 701 may be a first organic material layer
  • the electron transport layer 501 may be a second organic material layer.
  • an electron injection and transport layer may be introduced instead of the electron transport layer 501 in FIG. 2.
  • the electron injection and transport layer may mean a layer that simultaneously performs electron injection and transport, and a material of the electron injection layer and / or the electron transport layer may be used as the material of the electron injection and transport layer.
  • an anode 201, a hole transport layer 301, a first light emitting layer 402, a second light emitting layer 403, a hole blocking layer 701, an electron transport layer 501, and a cathode 601 are disposed on a substrate 101.
  • the structure of this sequentially laminated organic light emitting element is illustrated.
  • the hole blocking layer 701 may be a first organic material layer
  • the electron transport layer 501 may be a second organic material layer
  • the second light emitting layer 402 and the first light emitting layer 403 may be provided in contact with each other.
  • an additional organic layer may be provided.
  • an anode 201 and a hole transport layer 301 are provided on the substrate 101, and a first light emitting layer 402 and a second light emitting layer 403 are provided on the hole transport layer 301.
  • the structure of the organic light emitting device in which the hole blocking layer 701, the electron transport layer 501, and the cathode 601 are sequentially stacked on the light emitting layer 402 and the second light emitting layer 403 is illustrated.
  • the hole blocking layer 701 may be a first organic material layer
  • the electron transport layer 501 may be a second organic material layer.
  • FIG. 5 shows an anode 201, a hole transport layer 301, a first light emitting layer 402, a second light emitting layer 403, a third light emitting layer 404, a hole blocking layer 701, and an electron transport layer on a substrate 101.
  • the structure of the organic light emitting device in which the 501 and the cathode 601 are sequentially stacked is illustrated.
  • the hole blocking layer 701 may be a first organic material layer
  • the electron transport layer 501 may be the second organic material layer.
  • the first light emitting layer 402, the second light emitting layer 403, and the second material may be formed.
  • the third light emitting layer 404 may be provided in contact with each other, and may be added between the first light emitting layer 402 and the second light emitting layer 403 and / or between the second light emitting layer 403 and the third light emitting layer 404.
  • the organic material layer may be provided.
  • 1 to 5 are exemplary structures according to the exemplary embodiment of the present specification, and may further include other organic material layers. 1 to 5, the first organic compound layer may be an electron injection layer or an electron injection and transport layer instead of the electron transport layer 501.
  • the organic light emitting diode of the present specification includes a first organic material layer including the compound represented by Formula 1 between the cathode and the light emitting layer, and includes a second organic material layer represented by Formula 2 between the cathode and the first organic material layer. Except that it can be prepared with materials and methods known in the art.
  • the organic light emitting device of the present specification may be manufactured by sequentially stacking an anode, an organic material layer, and a cathode on a substrate. At this time, by using a 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, an electron blocking layer, a light emitting layer, an electron transport layer, and an electron injection layer thereon, and then depositing a material that can be used as a cathode 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.
  • an organic light emitting device may be manufactured by sequentially depositing an anode material, an organic material layer, and a cathode material on a substrate.
  • the organic material layer of the organic light emitting device of the present specification may have a multilayer structure in which one or more organic material layers are stacked.
  • the organic light emitting device includes one or two or more layers selected from the group consisting of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer, an electron blocking layer, and a hole blocking layer. It may further include.
  • the organic material layers may be formed of the same material or different materials.
  • the anode material a material having a large work function is usually preferred to facilitate hole injection into the organic material layer.
  • the positive electrode material that can be used in the present invention include metals such as vanadium, chromium, copper, zinc and gold or alloys thereof; Metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), indium zinc oxide (IZO); ZnO: Al or SNO 2 : Combination of metals and oxides such as 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 generally 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 material is a layer for injecting holes from an electrode, and the hole injection material has a capability of transporting holes.
  • the hole injection material has a hole injection effect at an anode, and has an excellent hole injection effect for a light emitting layer or a light emitting material.
  • the compound which prevents the movement of the excited excitons 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 material 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 electron blocking layer is a layer which can prevent the electrons injected from the electron injection layer from passing through the light emitting layer to the hole injection layer to improve the life and efficiency of the device, and if necessary, using a known material using a known material It may be formed in a suitable portion between injection layers.
  • the hole transport layer is a layer that receives holes from the hole injection layer and transports holes to the light emitting layer.
  • the hole transport material is a material capable of transporting holes from the anode or the hole injection layer to the light emitting layer.
  • the material 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 light emitting material may be formed by transporting and combining holes and electrons from the hole transporting layer and the electron transporting layer, respectively, to provide light in the visible light region.
  • the material which can be produced a material having good quantum efficiency for 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, benzothiazole and benzimidazole series compounds; Poly (p-phenylenevinylene) (PPV) -based polymers; Spiro compounds; Polyfluorene, rubrene and the like, but are not limited thereto.
  • Alq 3 8-hydroxyquinoline aluminum complex
  • Carbazole series compounds Dimerized styryl compounds
  • BAlq 10-hydroxybenzo quinoline-metal compound
  • Benzoxazole benzothiazole 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 fluorescent light emitting layer may be distyrylarylene (DSA), distyrylarylene derivative, distyrylbenzene (DSB), distyrylbenzene derivative, or DPVBi (4,4'-bis (2,2 ') as a host material. 1 or 2 or more are selected from the group consisting of -diphenyl vinyl) -1,1'-biphenyl), DPVBi derivatives, spiro-DPVBi and spiro-6sexy (spiro-sexyphenyl).
  • the fluorescent layer is selected from the group consisting of styrylamine, perylene, and DSBP (distyrylbiphenyl) as a dopant material.
  • the electron injection layer is a layer that injects electrons from an electrode, has an ability of transporting electrons, has an electron injection effect from a cathode, an excellent electron injection effect on a light emitting layer or a 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.
  • the organic light emitting device comprises an additional electron injection layer other than the electron injection layer containing the compound represented by the formula (2), specifically, fluorenone, anthraquinomethane, diphenoquinone, thiopyran dioxide, oxa Sol, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, preorenylidene methane, anthrone and the like and derivatives thereof, metal complex compounds and nitrogen-containing five-membered ring derivatives, and the like, but are not limited thereto.
  • the compound represented by the formula (2) specifically, fluorenone, anthraquinomethane, diphenoquinone, thiopyran dioxide, oxa Sol, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, preorenylidene methane, anthrone and the like and derivatives thereof, metal complex compounds and nitrogen-containing five-membered ring derivative
  • 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 electron transport layer is a layer that receives electrons from the electron injection layer and transports electrons to the light emitting layer, when the organic light emitting device includes an additional electron transport layer other than the electron transport layer containing a compound represented by the formula (2),
  • a transport material a material capable of injecting electrons well from the cathode and transferring the electrons to the light emitting layer is suitable. Specific examples thereof 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, each followed by an aluminum or silver layer.
  • the hole blocking layer is a layer which blocks the reaching of the cathode of the hole, and may generally be formed under the same conditions as the hole injection layer.
  • the organic light emitting device may be a top emission type, a bottom emission type, or a double-sided emission type according to a material used.
  • the organic light emitting device may be a normal type in which the lower electrode is an anode and the upper electrode is a cathode, or may be an inverted type in which the lower electrode is a cathode and the upper electrode is an anode.
  • the structure according to the exemplary embodiment of the present specification may act on a principle similar to that applied to an organic light emitting device in an organic electronic device including an organic solar cell, an organic photoconductor, an organic transistor, and the like.
  • a method for synthesizing the compound represented by Chemical Formula 1 according to an exemplary embodiment of the present invention will be described using the method for synthesizing Compound 1-1 as an example.
  • naphthalen-1-ol instead of 4-bromophenol in the synthesis of compound 1A enables synthesis of the same core as compound 1B below.
  • the synthesis method of the compound represented by the formula (1) is not limited to the above method, it may be by other methods.
  • a glass substrate (corning 7059 glass) coated with a thin film of ITO (indium tin oxide) to a thickness of 100 nm was placed in distilled water in which a dispersant was dissolved and washed with ultrasonic waves. Fischer Co. was used for the detergent, and Millipore Co. Secondary filtered distilled water was used as a filter of the product. After ITO was washed for 30 minutes, ultrasonic washing was performed twice with distilled water for 10 minutes. After washing the distilled water, the ultrasonic washing in the order of isopropyl alcohol, acetone, methanol solvent and dried.
  • ITO indium tin oxide
  • Hexonitrile hexaazatriphenylene (HAT-CN; hexanitrile hexaazatriphenylene) was thermally vacuum deposited to a thickness of 50 nm on the prepared ITO transparent electrode to form a hole injection layer.
  • Compound HT1 was vacuum deposited to a thickness of 40 nm thereon to form a hole transport layer.
  • the host compound BH1 and the dopant compound BD1 were vacuum deposited on the hole transport layer at a weight ratio of 97.5: 2.5 to form a light emitting layer having a thickness of 30 nm.
  • Compound 1-1 was deposited on the emission layer to form a hole blocking layer (electron control layer) having a thickness of 5 nm, and compound 2-1 and LiQ (Lithium Quinolate) were vacuum-deposited at a weight ratio of 1: 1 to 35 nm in thickness.
  • the electron injection and transport layer of was formed.
  • Lithium fluoride (LiF) and aluminum were sequentially deposited on the electron injection and transport layer at a thickness of 1.2 nm to form a cathode.
  • An organic light emitting device was manufactured.
  • An organic light emitting diode was manufactured according to the same method as Example 1-1 except for using the compound of Table 1 instead of the compound 1-1 and 2-1.
  • An organic light-emitting device was manufactured in the same manner as in Example 1-1, except that the electron injection and transport layer was not formed.
  • An organic light-emitting device was manufactured in the same manner as in Example 1-1, except that the hole blocking layer was not formed.
  • An organic light emitting diode was manufactured according to the same method as Example 1-1 except for using Compound 1-3 instead of Compound 1-1 in the hole blocking layer and Compound NPD instead of Compound 2-1 in the electron injection and transport layer. .
  • the luminous efficiency of the organic light emitting device manufactured in the Experimental Example was measured at a current density of 10 mA / cm 2 , and a time (LT98) of 98% of the initial luminance was measured at a current density of 20 mA / cm 2 .
  • the results are shown in Table 1 below.
  • the organic light emitting device including both the first organic material layer including the compound of Formula 1 and the second organic material layer including the compound of Formula 2 has a reduced driving voltage, improved efficiency, and particularly life characteristics. This can be seen to be greatly improved.

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