WO2023224020A1 - Composé, matériau d'élément électroluminescent organique, élément électroluminescent organique et dispositif électronique - Google Patents

Composé, matériau d'élément électroluminescent organique, élément électroluminescent organique et dispositif électronique Download PDF

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WO2023224020A1
WO2023224020A1 PCT/JP2023/018193 JP2023018193W WO2023224020A1 WO 2023224020 A1 WO2023224020 A1 WO 2023224020A1 JP 2023018193 W JP2023018193 W JP 2023018193W WO 2023224020 A1 WO2023224020 A1 WO 2023224020A1
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substituted
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佑典 高橋
裕亮 糸井
将太 田中
司 澤藤
拓人 深見
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出光興産株式会社
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    • C07C211/57—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton
    • C07C211/61—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton with at least one of the condensed ring systems formed by three or more rings
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    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
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    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
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    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
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    • 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
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    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
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    • H10K50/14—Carrier transporting layers
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    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
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Definitions

  • the present invention relates to a compound, a material for an organic electroluminescent device, an organic electroluminescent device, and an electronic device including the organic electroluminescent device.
  • an organic electroluminescent device (hereinafter sometimes referred to as an "organic EL device") is composed of an anode, a cathode, and an organic layer sandwiched between the anode and the cathode.
  • an organic EL device When a voltage is applied between the two electrodes, electrons are injected from the cathode side and holes from the anode side into the light emitting region, and the injected electrons and holes recombine in the light emitting region to generate an excited state. Light is emitted when the state returns to the ground state. Therefore, finding a combination of materials that efficiently transports electrons or holes to the light-emitting region, facilitates the recombination of electrons and holes, and efficiently issues excitons is essential in obtaining high-performance organic EL devices. is important.
  • Patent Documents 1 to 13 disclose compounds used as materials for organic electroluminescent devices.
  • the present invention was made to solve the above problems, and provides a compound that further improves the performance of an organic EL element, an organic EL element with further improved element performance, and an electronic device including such an organic EL element.
  • the purpose is to provide.
  • the present invention provides a compound represented by the following formula (1).
  • N * is the central nitrogen atom.
  • One of R a and R b is a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, and the other is a substituted or unsubstituted aryl group having 6 to 30 ring forming carbon atoms, or a substituted or unsubstituted ring It is a heterocyclic group having 5 to 30 atoms.
  • R a and R b may be combined with each other to form a substituted or unsubstituted ring.
  • R 2 , R 3 , R 6 and R 7 is a single bond that is bonded to *1, and R that is not a single bond that is bonded to R 1 , R 4 , R 5 , R 8 and *1 2 , R 3 , R 6 and R 7 are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, or a substituted or unsubstituted cycloalkyl group having 3 to 15 ring carbon atoms. , a substituted or unsubstituted aryl group having 6 to 12 ring atoms, or a substituted or unsubstituted heterocyclic group having 5 to 13 ring atoms.
  • Ar 1 and Ar 2 are groups represented by any of the following formulas (1a) to (1g).
  • *21 is the bonding position to L 1 or L 2 .
  • One selected from R 101 to R 105 is a single bond bonded to *22, and one selected from R 106 to R 110 is a single bond bonded to *23, selected from R 111 to R 115 .
  • Each of R 101 to R 115 that is not a single bond is independently a hydrogen atom, an unsubstituted alkyl group having 1 to 10 carbon atoms, or an unsubstituted aryl group having 6 to 12 ring carbon atoms.
  • R 116 to R 120 are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms, or a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms; is a heterocyclic group having 5 to 13 ring atoms.
  • Two adjacent ones selected from R 116 to R 120 do not bond to each other and therefore do not form a ring.
  • *25 is the bonding position to L 1 or L 2 .
  • One selected from R 121 to R 128 is a single bond bonded to *26.
  • R 121 to R 128 which are not single bonds are each independently a hydrogen atom, an unsubstituted alkyl group having 1 to 10 carbon atoms, or an unsubstituted aryl group having 6 to 12 ring carbon atoms. Two adjacent ones selected from R 121 to R 128 that are not single bonds do not bond to each other and therefore do not form a ring.
  • Each of R 131 to R 140 that is not a single bond is independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms, or a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms. It is. Two adjacent ones selected from R 131 to R 140 that are not single bonds do not bond to each other and therefore do not form a ring. ) (In formula (1d), *29 is the bonding position to L 1 or L 2 . One selected from R 141 to R 152 is a single bond bonded to *30.
  • R 141 to R 152 which are not single bonds are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms, or a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms. It is. Two adjacent ones selected from R 141 to R 152 that are not single bonds do not bond to each other and therefore do not form a ring structure. ) (In formula (1e), *31 is the bonding position to L 1 or L 2 . One selected from R 161 to R 165 is a single bond bonded to *32, and the other selected from R 161 to R 165 is a single bond bonded to *33.
  • R 161 to R 165 which are neither a single bond bonded to *32 nor a single bond bonded to *33 are each independently a hydrogen atom, an unsubstituted alkyl group having 1 to 10 carbon atoms, or an unsubstituted alkyl group having 1 to 10 carbon atoms. It is a substituted phenyl group.
  • Two adjacent ones selected from R 161 to R 165 that are neither a single bond bonded to *32 nor a single bond bonded to *33 do not bond to each other and therefore do not form a ring.
  • R 171 to R 175 and R 181 to R 185 each independently represent a hydrogen atom or an unsubstituted alkyl group having 1 to 10 carbon atoms.
  • R 171 to R 175 Two adjacent ones selected from R 171 to R 175 may be bonded to each other to form one or more unsubstituted benzene rings, or may not be bonded to each other and therefore do not form a ring
  • Two adjacent ones selected from R 181 to R 185 may be bonded to each other to form one or more unsubstituted benzene rings, or may not be bonded to each other and therefore do not form a ring.
  • *34 is the bonding position to L 1 or L 2 .
  • X is an oxygen atom, a sulfur atom, or NRA .
  • R 191 to R 198 and R A is a single bond bonded to *35.
  • R A that is not a single bond is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms.
  • R 191 to R 198 that are not single bonds are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 ring-forming carbon atoms, or a substituted or unsubstituted heterocyclic group having 5 to 13 ring atoms.
  • R 191 to R 198 Two adjacent ones selected from R 191 to R 198 that are not single bonds may be bonded to each other to form one or more unsubstituted benzene rings, or may not be bonded to each other and therefore form a ring. You don't have to. ) (In formula (1g), *36 is the bonding position to L 1 or L 2 . One selected from R B , R C , and R 201 to R 208 is a single bond bonded to *37.
  • R B and R C which are not single bonds are each independently a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms, or a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms; It is an unsubstituted heterocyclic group having 5 to 13 ring atoms.
  • R B and R C which are not single bonds, may be bonded to each other to form a substituted or unsubstituted ring.
  • R 201 to R 208 which are not single bonds are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms, or a substituted or unsubstituted heterocyclic group having 5 to 13 ring atoms.
  • Two adjacent ones selected from R 201 to R 208 that are not single bonds do not bond to each other and therefore do not form a ring. ))
  • the present invention provides a material for an organic EL device containing a compound represented by the above formula (1).
  • the invention provides an organic electroluminescent device comprising a cathode, an anode, and an organic layer between the cathode and the anode, the organic layer comprising a light-emitting layer, and at least one of the organic layers.
  • An organic electroluminescent device in which one layer contains a compound represented by the formula (1) is provided.
  • the present invention provides an electronic device including the organic electroluminescent device.
  • An organic EL device containing the compound represented by formula (1) above exhibits improved device performance.
  • FIG. 1 is a schematic diagram showing an example of a layer structure of an organic EL element according to one embodiment of the present invention.
  • FIG. 3 is a schematic diagram illustrating another example of the layer structure of an organic EL element according to one embodiment of the present invention.
  • FIG. 3 is a schematic diagram showing still another example of the layer structure of an organic EL element according to one embodiment of the present invention.
  • the hydrogen atom includes isotopes having different numbers of neutrons, ie, light hydrogen (protium), deuterium (deuterium), and tritium (tritium).
  • a hydrogen atom that is, a light hydrogen atom, a deuterium atom, or Assume that tritium atoms are bonded.
  • the number of carbon atoms forming a ring refers to the number of carbon atoms constituting the ring itself of a compound having a structure in which atoms are bonded in a cyclic manner (for example, a monocyclic compound, a condensed ring compound, a bridged compound, a carbocyclic compound, and a heterocyclic compound). represents the number of carbon atoms among the atoms.
  • a monocyclic compound, a condensed ring compound, a bridged compound, a carbocyclic compound, and a heterocyclic compound represents the number of carbon atoms among the atoms.
  • the carbon contained in the substituent is not included in the number of carbon atoms forming the ring.
  • the "number of ring carbon atoms" described below is the same unless otherwise specified.
  • a benzene ring has 6 carbon atoms
  • a naphthalene ring has 10 carbon atoms
  • a pyridine ring has 5 carbon atoms
  • a furan ring has 4 carbon atoms.
  • the number of ring carbon atoms in the 9,9-diphenylfluorenyl group is 13
  • the number of ring carbon atoms in the 9,9'-spirobifluorenyl group is 25.
  • the benzene ring is substituted with an alkyl group as a substituent, for example, the number of carbon atoms of the alkyl group is not included in the number of carbon atoms forming the benzene ring.
  • the number of ring carbon atoms in the benzene ring substituted with an alkyl group is 6. Further, when the naphthalene ring is substituted with an alkyl group as a substituent, for example, the number of carbon atoms of the alkyl group is not included in the number of carbon atoms forming the naphthalene ring. Therefore, the number of ring carbon atoms in the naphthalene ring substituted with an alkyl group is 10.
  • the number of ring-forming atoms refers to compounds with a structure in which atoms are bonded in a cyclic manner (e.g., monocyclic, fused ring, and ring assembly) (e.g., monocyclic compound, fused ring compound, bridged compound, carbocyclic compound). Represents the number of atoms that constitute the ring itself (compounds and heterocyclic compounds). Atoms that do not form a ring (for example, a hydrogen atom that terminates a bond between atoms that form a ring) and atoms that are included in a substituent when the ring is substituted with a substituent are not included in the number of ring-forming atoms.
  • the "number of ring-forming atoms" described below is the same unless otherwise specified.
  • the number of ring atoms in the pyridine ring is 6, the number of ring atoms in the quinazoline ring is 10, and the number of ring atoms in the furan ring is 5.
  • the number of hydrogen atoms bonded to the pyridine ring or atoms constituting substituents is not included in the number of atoms forming the pyridine ring. Therefore, the number of ring atoms of the pyridine ring to which hydrogen atoms or substituents are bonded is six.
  • carbon number XX to YY in the expression “substituted or unsubstituted ZZ group with carbon number XX to YY” represents the number of carbon atoms when the ZZ group is unsubstituted, and is substituted. Do not include the number of carbon atoms in substituents.
  • "YY" is larger than “XX”, “XX” means an integer of 1 or more, and “YY” means an integer of 2 or more.
  • number of atoms XX to YY in the expression “substituted or unsubstituted ZZ group with number of atoms XX to YY” represents the number of atoms when the ZZ group is unsubstituted, and is substituted. Do not include the number of atoms of substituents in case.
  • "YY" is larger than “XX”, “XX” means an integer of 1 or more, and "YY" means an integer of 2 or more.
  • an unsubstituted ZZ group refers to a case where a "substituted or unsubstituted ZZ group" is an "unsubstituted ZZ group", and a substituted ZZ group refers to a "substituted or unsubstituted ZZ group". represents the case where is a "substituted ZZ group".
  • "unsubstituted” in the case of "substituted or unsubstituted ZZ group” means that the hydrogen atom in the ZZ group is not replaced with a substituent.
  • the hydrogen atom in the "unsubstituted ZZ group” is a light hydrogen atom, a deuterium atom, or a tritium atom.
  • substituted in the case of “substituted or unsubstituted ZZ group” means that one or more hydrogen atoms in the ZZ group are replaced with a substituent.
  • substitution in the case of "BB group substituted with an AA group” similarly means that one or more hydrogen atoms in the BB group are replaced with an AA group.
  • the number of ring carbon atoms in the "unsubstituted aryl group” described herein is 6 to 50, preferably 6 to 30, more preferably 6 to 18, unless otherwise specified herein. .
  • the number of ring atoms of the "unsubstituted heterocyclic group” described herein is 5 to 50, preferably 5 to 30, more preferably 5 to 18, unless otherwise specified herein. be.
  • the number of carbon atoms in the "unsubstituted alkyl group” described herein is 1 to 50, preferably 1 to 20, more preferably 1 to 6, unless otherwise specified herein.
  • the number of carbon atoms in the "unsubstituted alkenyl group” described herein is 2 to 50, preferably 2 to 20, more preferably 2 to 6, unless otherwise specified herein.
  • the number of carbon atoms in the "unsubstituted alkynyl group” described herein is 2 to 50, preferably 2 to 20, more preferably 2 to 6, unless otherwise specified herein.
  • the number of ring carbon atoms in the "unsubstituted cycloalkyl group” described herein is 3 to 50, preferably 3 to 20, more preferably 3 to 6. be.
  • the number of ring carbon atoms in the "unsubstituted arylene group” described herein is 6 to 50, preferably 6 to 30, more preferably 6 to 18. .
  • the number of ring atoms of the "unsubstituted divalent heterocyclic group” described herein is 5 to 50, preferably 5 to 30, more preferably 5 unless otherwise specified herein. ⁇ 18.
  • the number of carbon atoms in the "unsubstituted alkylene group” described herein is 1 to 50, preferably 1 to 20, more preferably 1 to 6, unless otherwise specified herein.
  • Specific examples (specific example group G1) of the "substituted or unsubstituted aryl group” described in this specification include the following unsubstituted aryl groups (specific example group G1A) and substituted aryl groups (specific example group G1B). ) etc.
  • the unsubstituted aryl group refers to the case where the "substituted or unsubstituted aryl group” is an "unsubstituted aryl group"
  • the substituted aryl group refers to the case where the "substituted or unsubstituted aryl group” is (Refers to the case where it is a "substituted aryl group.)
  • aryl group includes both "unsubstituted aryl group” and “substituted aryl group.”
  • “Substituted aryl group” means a group in which one or more hydrogen atoms of "unsubstituted aryl group” are replaced with a substituent.
  • Examples of the "substituted aryl group” include a group in which one or more hydrogen atoms of the "unsubstituted aryl group” in the specific example group G1A below are replaced with a substituent, and a substituted aryl group in the following specific example group G1B. Examples include: The examples of “unsubstituted aryl group” and “substituted aryl group” listed here are just examples, and the "substituted aryl group” described in this specification includes the following specific examples.
  • aryl group (specific example group G1A): phenyl group, p-biphenyl group, m-biphenyl group, o-biphenyl group, p-terphenyl-4-yl group, p-terphenyl-3-yl group, p-terphenyl-2-yl group, m-terphenyl-4-yl group, m-terphenyl-3-yl group, m-terphenyl-2-yl group, o-terphenyl-4-yl group, o-terphenyl-3-yl group, o-terphenyl-2-yl group, 1-naphthyl group, 2-naphthyl group, anthryl group, benzanthryl group, phenanthryl group, benzophenanthryl group, phenalenyl group, pyrenyl group, chrysenyl group, benzocrysenyl group,
  • aryl group (specific example group G1B): o-tolyl group, m-tolyl group, p-tolyl group, para-xylyl group, meta-xylyl group, ortho-xylyl group, para-isopropylphenyl group, meta-isopropylphenyl group, ortho-isopropylphenyl group, para-t-butylphenyl group, meta-t-butylphenyl group, ortho-t-butylphenyl group, 3,4,5-trimethylphenyl group, 9,9-dimethylfluorenyl group, 9,9-diphenylfluorenyl group 9,9-bis(4-methylphenyl)fluorenyl group, 9,9-bis(4-isopropylphenyl)fluorenyl group, 9,9-bis(4-t-butylphenyl)fluorenyl group, cyanophenyl group, triphenylsily
  • heterocyclic group is a cyclic group containing at least one heteroatom as a ring-forming atom. Specific examples of heteroatoms include nitrogen atom, oxygen atom, sulfur atom, silicon atom, phosphorus atom, and boron atom.
  • a “heterocyclic group” as described herein is a monocyclic group or a fused ring group.
  • a “heterocyclic group” as described herein is an aromatic heterocyclic group or a non-aromatic heterocyclic group.
  • substituted or unsubstituted heterocyclic group examples include the following unsubstituted heterocyclic group (specific example group G2A) and substituted heterocyclic group ( Examples include specific example group G2B).
  • unsubstituted heterocyclic group refers to the case where "substituted or unsubstituted heterocyclic group” is “unsubstituted heterocyclic group”
  • substituted heterocyclic group refers to "substituted or unsubstituted heterocyclic group”
  • Heterocyclic group refers to a "substituted heterocyclic group."
  • heterocyclic group refers to "unsubstituted heterocyclic group” and “substituted heterocyclic group.” including both.
  • “Substituted heterocyclic group” means a group in which one or more hydrogen atoms of "unsubstituted heterocyclic group” are replaced with a substituent.
  • Specific examples of the "substituted heterocyclic group” include a group in which the hydrogen atom of the "unsubstituted heterocyclic group” in specific example group G2A is replaced, and examples of substituted heterocyclic groups in specific example group G2B below. Can be mentioned.
  • Specific example group G2A includes, for example, the following unsubstituted heterocyclic groups containing a nitrogen atom (specific example group G2A1), unsubstituted heterocyclic groups containing an oxygen atom (specific example group G2A2), and unsubstituted heterocyclic groups containing a sulfur atom.
  • heterocyclic group (specific example group G2A3), and a monovalent heterocyclic group derived by removing one hydrogen atom from the ring structure represented by the following general formulas (TEMP-16) to (TEMP-33) (Specific example group G2A4).
  • Specific example group G2B includes, for example, the following substituted heterocyclic groups containing a nitrogen atom (specific example group G2B1), substituted heterocyclic groups containing an oxygen atom (specific example group G2B2), and substituted heterocyclic groups containing a sulfur atom.
  • group Specific Example Group G2B3
  • one or more hydrogen atoms of a monovalent heterocyclic group derived from a ring structure represented by the following general formulas (TEMP-16) to (TEMP-33) are substituents.
  • Includes substituted groups (Example Group G2B4).
  • ⁇ Unsubstituted heterocyclic group containing a nitrogen atom (specific example group G2A1): pyrrolyl group, imidazolyl group, pyrazolyl group, triazolyl group, Tetrazolyl group, oxazolyl group, isoxazolyl group, oxadiazolyl group, thiazolyl group, isothiazolyl group, thiadiazolyl group, pyridyl group, pyridazinyl group, pyrimidinyl group, pyrazinyl group, triazinyl group, indolyl group, isoindolyl group, indolizinyl group, quinolidinyl group, quinolyl group, isoquinolyl group, cinnolyl group, phthalazinyl group, quinazolinyl group, quinoxalinyl group, benzimidazolyl group, indazolyl group, phenanthrolinyl
  • ⁇ Unsubstituted heterocyclic group containing an oxygen atom (specific example group G2A2): frill group, oxazolyl group, isoxazolyl group, oxadiazolyl group, xanthenyl group, benzofuranyl group, isobenzofuranyl group, dibenzofuranyl group, naphthobenzofuranyl group, benzoxazolyl group, benzisoxazolyl group, phenoxazinyl group, morpholino group, dinaphthofuranyl group, azadibenzofuranyl group, diazadibenzofuranyl group, Azanaphthobenzofuranyl group, and diazanaphthobenzofuranyl group.
  • X A and Y A are each independently an oxygen atom, a sulfur atom, NH, or CH 2 . However, at least one of X A and Y A is an oxygen atom, a sulfur atom, or NH.
  • the monovalent heterocyclic group derived from the represented ring structure includes a monovalent group obtained by removing one hydrogen atom from these NH or CH 2 .
  • Substituted heterocyclic group containing a nitrogen atom (specific example group G2B1): (9-phenyl)carbazolyl group, (9-biphenylyl)carbazolyl group, (9-phenyl)phenylcarbazolyl group, (9-naphthyl)carbazolyl group, diphenylcarbazol-9-yl group, phenylcarbazol-9-yl group, methylbenzimidazolyl group, ethylbenzimidazolyl group, phenyltriazinyl group, biphenylyltriazinyl group, diphenyltriazinyl group, phenylquinazolinyl group, and biphenylylquinazolinyl group.
  • ⁇ Substituted heterocyclic group containing an oxygen atom (specific example group G2B2): phenyldibenzofuranyl group, methyldibenzofuranyl group, A t-butyldibenzofuranyl group and a monovalent residue of spiro[9H-xanthene-9,9'-[9H]fluorene].
  • ⁇ Substituted heterocyclic group containing a sulfur atom (specific example group G2B3): phenyldibenzothiophenyl group, methyldibenzothiophenyl group, A t-butyldibenzothiophenyl group and a monovalent residue of spiro[9H-thioxanthene-9,9'-[9H]fluorene].
  • one or more hydrogen atoms of a monovalent heterocyclic group refers to a hydrogen atom bonded to a ring-forming carbon atom of the monovalent heterocyclic group, and at least one of XA and YA is NH. It means one or more hydrogen atoms selected from the hydrogen atom bonded to the nitrogen atom in the case where XA and YA are CH2, and the hydrogen atom of the methylene group when one of XA and YA is CH2.
  • Specific examples (specific example group G3) of the "substituted or unsubstituted alkyl group" described in this specification include the following unsubstituted alkyl groups (specific example group G3A) and substituted alkyl groups (specific example group G3B). ).
  • an unsubstituted alkyl group refers to a case where a "substituted or unsubstituted alkyl group” is an "unsubstituted alkyl group," and a substituted alkyl group refers to a case where a "substituted or unsubstituted alkyl group” is (This refers to the case where it is a "substituted alkyl group.”)
  • alkyl group when it is simply referred to as an "alkyl group,” it includes both an "unsubstituted alkyl group” and a "substituted alkyl group.”
  • “Substituted alkyl group” means a group in which one or more hydrogen atoms in "unsubstituted alkyl group” are replaced with a substituent.
  • substituted alkyl group examples include groups in which one or more hydrogen atoms in the "unsubstituted alkyl group” (specific example group G3A) below are replaced with a substituent, and substituted alkyl groups (specific examples examples include group G3B).
  • the alkyl group in "unsubstituted alkyl group” means a chain alkyl group. Therefore, the "unsubstituted alkyl group” includes a linear "unsubstituted alkyl group” and a branched "unsubstituted alkyl group”.
  • ⁇ Unsubstituted alkyl group (specific example group G3A): methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, s-butyl group and t-butyl group.
  • ⁇ Substituted alkyl group (specific example group G3B): heptafluoropropyl group (including isomers), pentafluoroethyl group, 2,2,2-trifluoroethyl group and trifluoromethyl group.
  • “Substituted or unsubstituted alkenyl group” Specific examples of the "substituted or unsubstituted alkenyl group" (specific example group G4) described in this specification include the following unsubstituted alkenyl groups (specific example group G4A) and substituted alkenyl groups (specific example group G4B), etc.
  • the term "unsubstituted alkenyl group” refers to the case where "substituted or unsubstituted alkenyl group” is “unsubstituted alkenyl group”
  • “substituted alkenyl group” refers to "substituted or unsubstituted alkenyl group”).
  • alkenyl group includes both “unsubstituted alkenyl group” and “substituted alkenyl group.”
  • Substituted alkenyl group means a group in which one or more hydrogen atoms in "unsubstituted alkenyl group” are replaced with a substituent.
  • Specific examples of the "substituted alkenyl group” include the following "unsubstituted alkenyl group” (specific example group G4A) having a substituent, and the substituted alkenyl group (specific example group G4B). It will be done.
  • ⁇ Unsubstituted alkenyl group (specific example group G4A): vinyl group, allyl group, 1-butenyl group, 2-butenyl group and 3-butenyl group.
  • ⁇ Substituted alkenyl group (specific example group G4B): 1,3-butandienyl group, 1-methylvinyl group, 1-methylallyl group, 1,1-dimethylallyl group, 2-methylallyl group and 1,2-dimethylallyl group.
  • unsubstituted alkynyl group refers to the case where "substituted or unsubstituted alkynyl group” is “unsubstituted alkynyl group."
  • "unsubstituted alkynyl group” is referred to as "unsubstituted alkynyl group.”
  • ⁇ alkynyl group'' and ⁇ substituted alkynyl group.'' "Substituted alkynyl group” means a group in which one or more hydrogen atoms in "unsubstituted alkynyl group” are replaced with a substituent.
  • Specific examples of the "substituted alkynyl group” include groups in which one or more hydrogen atoms in the following "unsubstituted alkynyl group” (specific example group G5A) are replaced with a substituent.
  • Specific examples (specific example group G6) of the "substituted or unsubstituted cycloalkyl group” described in this specification include the following unsubstituted cycloalkyl groups (specific example group G6A) and substituted cycloalkyl groups ( Examples include specific example group G6B).
  • unsubstituted cycloalkyl group refers to the case where "substituted or unsubstituted cycloalkyl group” is “unsubstituted cycloalkyl group”, and the term “substituted cycloalkyl group” refers to "substituted or unsubstituted cycloalkyl group”).
  • cycloalkyl group refers to the case where "substituted cycloalkyl group” is used.
  • cycloalkyl group when simply referring to “cycloalkyl group”, it refers to "unsubstituted cycloalkyl group” and “substituted cycloalkyl group”. including both.
  • Substituted cycloalkyl group means a group in which one or more hydrogen atoms in "unsubstituted cycloalkyl group” are replaced with a substituent.
  • Specific examples of the "substituted cycloalkyl group” include the following "unsubstituted cycloalkyl group” (specific example group G6A) in which one or more hydrogen atoms are replaced with a substituent, and a substituted cycloalkyl group. (Specific example group G6B) and the like can be mentioned.
  • cycloalkyl group (specific example group G6A): cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, 1-adamantyl group, 2-adamantyl group, 1-norbornyl group and 2-norbornyl group.
  • cycloalkyl group (specific example group G6B): 4-methylcyclohexyl group.
  • G7 Specific examples of the group represented by -Si(R 901 )(R 902 )(R 903 ) described in this specification (specific example group G7) include: -Si(G1)(G1)(G1), -Si (G1) (G2) (G2), -Si (G1) (G1) (G2), -Si(G2)(G2)(G2), -Si(G3)(G3)(G3), and -Si(G6)(G6)(G6) can be mentioned.
  • G1 is a "substituted or unsubstituted aryl group" described in specific example group G1.
  • G2 is a "substituted or unsubstituted heterocyclic group” described in specific example group G2.
  • G3 is a "substituted or unsubstituted alkyl group” described in specific example group G3.
  • G6 is a "substituted or unsubstituted cycloalkyl group” described in specific example group G6.
  • a plurality of G2's in Si(G2) (G2) (G2) are mutually the same or different.
  • a plurality of G3's in Si(G3) (G3) are mutually the same or different.
  • - A plurality of G6's in Si(G6) (G6) (G6) are mutually the same or different.
  • G8 Specific examples of the group represented by -O-(R 904 ) described in this specification (specific example group G8) include: -O(G1), -O(G2), -O (G3) and -O (G6) can be mentioned.
  • G1 is a "substituted or unsubstituted aryl group” described in specific example group G1.
  • G2 is a "substituted or unsubstituted heterocyclic group” described in specific example group G2.
  • G3 is a "substituted or unsubstituted alkyl group” described in specific example group G3.
  • G6 is a "substituted or unsubstituted cycloalkyl group” described in specific example group G6.
  • G9 Group represented by -S-(R 905 )
  • Specific examples of the group represented by -S-(R 905 ) described in this specification include: -S (G1), -S (G2), -S (G3) and -S (G6) can be mentioned.
  • G1 is a "substituted or unsubstituted aryl group” described in specific example group G1.
  • G2 is a "substituted or unsubstituted heterocyclic group” described in specific example group G2.
  • G3 is a "substituted or unsubstituted alkyl group” described in specific example group G3.
  • G6 is a "substituted or unsubstituted cycloalkyl group” described in specific example group G6.
  • G10 Group represented by -N(R 906 )(R 907 )
  • Specific examples of the group represented by -N(R 906 )(R 907 ) described in this specification include: -N(G1)(G1), -N(G2)(G2), -N (G1) (G2), -N (G3) (G3), and -N (G6) (G6) can be mentioned.
  • G1 is a "substituted or unsubstituted aryl group” described in specific example group G1.
  • G2 is a "substituted or unsubstituted heterocyclic group” described in specific example group G2.
  • G3 is a "substituted or unsubstituted alkyl group” described in specific example group G3.
  • G6 is a "substituted or unsubstituted cycloalkyl group” described in specific example group G6.
  • -N(G1) A plurality of G1's in (G1) are mutually the same or different.
  • -N(G2) A plurality of G2's in (G2) are the same or different.
  • -N(G3) A plurality of G3's in (G3) are mutually the same or different.
  • -N(G6) A plurality of G6's in (G6) are mutually the same or different.
  • halogen atom specifically examples include a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, and the like.
  • substituted or unsubstituted fluoroalkyl group refers to a "substituted or unsubstituted alkyl group" in which at least one hydrogen atom bonded to a carbon atom constituting the alkyl group is replaced with a fluorine atom. It also includes a group in which all hydrogen atoms bonded to the carbon atoms constituting the alkyl group in a "substituted or unsubstituted alkyl group” are replaced with fluorine atoms (perfluoro group).
  • the number of carbon atoms in the "unsubstituted fluoroalkyl group” is from 1 to 50, preferably from 1 to 30, and more preferably from 1 to 18, unless otherwise specified herein.
  • “Substituted fluoroalkyl group” means a group in which one or more hydrogen atoms of the "fluoroalkyl group” are replaced with a substituent.
  • substituted fluoroalkyl group described in this specification includes a group in which one or more hydrogen atoms bonded to the carbon atom of the alkyl chain in the "substituted fluoroalkyl group” is further replaced with a substituent, and Also included are groups in which one or more hydrogen atoms of a substituent in a "substituted fluoroalkyl group” are further replaced with a substituent.
  • substituents of a substituent in a "substituted fluoroalkyl group” are further replaced with a substituent.
  • the "unsubstituted fluoroalkyl group” include a group in which one or more hydrogen atoms in the "alkyl group” (specific example group G3) are replaced with a fluorine atom.
  • ⁇ “Substituted or unsubstituted haloalkyl group” means that at least one hydrogen atom bonded to a carbon atom constituting the alkyl group in the "substituted or unsubstituted alkyl group” is replaced with a halogen atom. It means a group, and also includes a group in which all hydrogen atoms bonded to carbon atoms constituting an alkyl group in a "substituted or unsubstituted alkyl group” are replaced with halogen atoms.
  • the number of carbon atoms in the "unsubstituted haloalkyl group” is from 1 to 50, preferably from 1 to 30, and more preferably from 1 to 18.
  • “Substituted haloalkyl group” means a group in which one or more hydrogen atoms of the "haloalkyl group” are replaced with a substituent.
  • the "substituted haloalkyl group" described in this specification includes a group in which one or more hydrogen atoms bonded to the carbon atom of the alkyl chain in the "substituted haloalkyl group” is further replaced with a substituent; Also included are groups in which one or more hydrogen atoms of a substituent in the "haloalkyl group” are further replaced with a substituent.
  • Specific examples of the "unsubstituted haloalkyl group” include a group in which one or more hydrogen atoms in the "alkyl group” (specific example group G3) are replaced with a halogen atom.
  • a haloalkyl group is sometimes referred to as a halogenated alkyl group.
  • a specific example of the "substituted or unsubstituted alkoxy group" described in this specification is a group represented by -O(G3), where G3 is a "substituted or unsubstituted alkoxy group” described in specific example group G3.
  • the number of carbon atoms in the "unsubstituted alkoxy group” is from 1 to 50, preferably from 1 to 30, and more preferably from 1 to 18, unless otherwise specified herein.
  • ⁇ “Substituted or unsubstituted alkylthio group” A specific example of the "substituted or unsubstituted alkylthio group” described in this specification is a group represented by -S(G3), where G3 is the "substituted or unsubstituted alkylthio group” described in specific example group G3. "unsubstituted alkyl group”. Unless otherwise specified herein, the number of carbon atoms in the "unsubstituted alkylthio group” is from 1 to 50, preferably from 1 to 30, and more preferably from 1 to 18.
  • a specific example of the "substituted or unsubstituted aryloxy group” described in this specification is a group represented by -O(G1), where G1 is a "substituted or unsubstituted aryloxy group” described in specific example group G1. or an unsubstituted aryl group.
  • the number of ring carbon atoms in the "unsubstituted aryloxy group" is from 6 to 50, preferably from 6 to 30, and more preferably from 6 to 18, unless otherwise specified herein.
  • a specific example of the "substituted or unsubstituted arylthio group” described in this specification is a group represented by -S(G1), where G1 is the "substituted or unsubstituted arylthio group” described in the specific example group G1.
  • G1 is the "substituted or unsubstituted arylthio group” described in the specific example group G1.
  • the number of ring carbon atoms in the "unsubstituted arylthio group” is from 6 to 50, preferably from 6 to 30, and more preferably from 6 to 18, unless otherwise specified herein.
  • ⁇ “Substituted or unsubstituted trialkylsilyl group” A specific example of the "trialkylsilyl group” described in this specification is a group represented by -Si(G3)(G3)(G3), where G3 is a group described in specific example group G3. It is a "substituted or unsubstituted alkyl group.” - A plurality of G3's in Si(G3) (G3) (G3) are mutually the same or different. The number of carbon atoms in each alkyl group of the "trialkylsilyl group” is from 1 to 50, preferably from 1 to 20, and more preferably from 1 to 6, unless otherwise specified herein.
  • a specific example of the "substituted or unsubstituted aralkyl group” described in this specification is a group represented by -(G3)-(G1), where G3 is a group described in specific example group G3. It is a "substituted or unsubstituted alkyl group", and G1 is a "substituted or unsubstituted aryl group” described in the specific example group G1.
  • an "aralkyl group” is a group in which the hydrogen atom of an "alkyl group” is replaced with an "aryl group” as a substituent, and is one embodiment of a “substituted alkyl group.”
  • An “unsubstituted aralkyl group” is an "unsubstituted alkyl group” substituted with an "unsubstituted aryl group”, and the number of carbon atoms in the "unsubstituted aralkyl group” is determined unless otherwise specified herein. , 7 to 50, preferably 7 to 30, more preferably 7 to 18.
  • substituted or unsubstituted aralkyl groups include benzyl group, 1-phenylethyl group, 2-phenylethyl group, 1-phenylisopropyl group, 2-phenylisopropyl group, phenyl-t-butyl group, ⁇ - Naphthylmethyl group, 1- ⁇ -naphthylethyl group, 2- ⁇ -naphthylethyl group, 1- ⁇ -naphthylisopropyl group, 2- ⁇ -naphthylisopropyl group, ⁇ -naphthylmethyl group, 1- ⁇ -naphthylethyl group , 2- ⁇ -naphthylethyl group, 1- ⁇ -naphthylisopropyl group, and 2- ⁇ -naphthylisopropyl group.
  • the substituted or unsubstituted aryl group described herein is preferably a phenyl group, p-biphenyl group, m-biphenyl group, o-biphenyl group, p-terphenyl group, unless otherwise specified herein.
  • Nanthrolinyl group carbazolyl group (1-carbazolyl group, 2-carbazolyl group, 3-carbazolyl group, 4-carbazolyl group, or 9-carbazolyl group), benzocarbazolyl group, azacarbazolyl group, diazacarbazolyl group , dibenzofuranyl group, naphthobenzofuranyl group, azadibenzofuranyl group, diazadibenzofuranyl group, dibenzothiophenyl group, naphthobenzothiophenyl group, azadibenzothiophenyl group, diazadibenzothiophenyl group, ( 9-phenyl)carbazolyl group ((9-phenyl)carbazol-1-yl group, (9-phenyl)carbazol-2-yl group, (9-phenyl)carbazol-3-yl group, or (9-phenyl)carbazole -4-yl group), (9-b
  • carbazolyl group is specifically any of the following groups unless otherwise specified in the specification.
  • the (9-phenyl)carbazolyl group is specifically any of the following groups, unless otherwise stated in the specification.
  • dibenzofuranyl group and dibenzothiophenyl group are specifically any of the following groups unless otherwise specified in the specification.
  • the substituted or unsubstituted alkyl group described herein is preferably a methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, and t- Butyl group, etc.
  • the "substituted or unsubstituted arylene group” described in this specification refers to 2 derived from the above “substituted or unsubstituted aryl group” by removing one hydrogen atom on the aryl ring. It is the basis of valence.
  • the "substituted or unsubstituted arylene group” (specific example group G12), by removing one hydrogen atom on the aryl ring from the "substituted or unsubstituted aryl group” described in specific example group G1
  • Examples include divalent groups derived from the derivatives.
  • the "substituted or unsubstituted divalent heterocyclic group” described herein refers to the "substituted or unsubstituted heterocyclic group" described above, in which one hydrogen atom on the heterocycle is removed. It is a divalent group derived from Specific examples of the "substituted or unsubstituted divalent heterocyclic group" (specific example group G13) include one hydrogen on the heterocycle from the "substituted or unsubstituted heterocyclic group” described in specific example group G2. Examples include divalent groups derived by removing atoms.
  • the "substituted or unsubstituted alkylene group” described in this specification refers to 2 derived from the above "substituted or unsubstituted alkyl group” by removing one hydrogen atom on the alkyl chain. It is the basis of valence.
  • a "substituted or unsubstituted alkylene group” (specific example group G14), one hydrogen atom on the alkyl chain is removed from the "substituted or unsubstituted alkyl group” described in specific example group G3. Examples include divalent groups derived from the derivatives.
  • the substituted or unsubstituted arylene group described herein is preferably a group represented by any of the following general formulas (TEMP-42) to (TEMP-68).
  • Q 1 to Q 10 are each independently a hydrogen atom or a substituent.
  • * represents the bonding position.
  • Q 1 to Q 10 are each independently a hydrogen atom or a substituent.
  • Formulas Q 9 and Q 10 may be bonded to each other via a single bond to form a ring.
  • * represents the bonding position.
  • Q 1 to Q 8 are each independently a hydrogen atom or a substituent.
  • * represents the bonding position.
  • the substituted or unsubstituted divalent heterocyclic group described herein is preferably one of the following general formulas (TEMP-69) to (TEMP-102), unless otherwise specified herein. It is.
  • Q 1 to Q 9 are each independently a hydrogen atom or a substituent.
  • Q 1 to Q 8 are each independently a hydrogen atom or a substituent.
  • the set of two or more adjacent R 930 is one set. is a set of R 921 and R 922 , a set of R 922 and R 923 , a set of R 923 and R 924 , a set of R 924 and R 930 , a set of R 930 and R 925 , a set of R 925 and A set of R 926 , a set of R 926 and R 927 , a set of R 927 and R 928 , a set of R 928 and R 929 , and a set of R 929 and R 921 .
  • the above-mentioned "one or more sets” means that two or more sets of the above-mentioned two or more adjacent sets may form a ring at the same time.
  • R 921 and R 922 combine with each other to form ring Q A
  • R 925 and R 926 combine with each other to form ring Q B
  • the above general formula (TEMP-103) The anthracene compound represented is represented by the following general formula (TEMP-104).
  • a set of two or more adjacent items forms a ring is not only the case where a set of "two" adjacent items are combined as in the example above, but also the case where a set of "three or more adjacent items” form a ring. This also includes the case where two sets are combined.
  • R 921 and R 922 combine with each other to form a ring Q A
  • R 922 and R 923 combine with each other to form a ring Q C
  • the three adjacent to each other (R 921 , R 922 and R 923 ) combine with each other to form a ring and are condensed to the anthracene mother skeleton.
  • anthracene compound represented by the general formula (TEMP-103) is as follows: It is represented by the general formula (TEMP-105). In the following general formula (TEMP-105), ring Q A and ring Q C share R 922 .
  • the "single ring” or “fused ring” that is formed may be a saturated ring or an unsaturated ring as the structure of only the formed ring. Even if “one set of two adjacent rings” forms a “monocycle” or “fused ring,” the “monocycle” or “fused ring” is a saturated ring, or Can form unsaturated rings.
  • ring Q A and ring Q B formed in the general formula (TEMP-104) are each a “monocyclic ring” or a “fused ring.”
  • the ring Q A and the ring Q C formed in the general formula (TEMP-105) are "fused rings”.
  • Ring Q A and ring Q C in the general formula (TEMP-105) are a condensed ring due to the condensation of ring Q A and ring Q C.
  • ring Q A in the general formula (TEMP-104) is a benzene ring
  • ring Q A is a monocyclic ring.
  • ring Q A in the general formula (TEMP-104) is a naphthalene ring
  • ring Q A is a fused ring.
  • Unsaturated ring means an aromatic hydrocarbon ring or an aromatic heterocycle.
  • “Saturated ring” means an aliphatic hydrocarbon ring or a non-aromatic heterocycle.
  • Specific examples of the aromatic hydrocarbon ring include structures in which the groups listed as specific examples in specific example group G1 are terminated with hydrogen atoms.
  • Specific examples of the aromatic heterocycle include structures in which the aromatic heterocyclic group listed as a specific example in specific example group G2 is terminated with a hydrogen atom.
  • Specific examples of the aliphatic hydrocarbon ring include structures in which the groups listed as specific examples in specific example group G6 are terminated with hydrogen atoms.
  • Form a ring means to form a ring with only a plurality of atoms of a parent skeleton, or with a plurality of atoms of a parent skeleton and one or more arbitrary elements.
  • the ring Q A shown in the general formula (TEMP-104) formed by R 921 and R 922 bonding to each other is a carbon atom of the anthracene skeleton to which R 921 is bonded, and an anthracene bond to which R 922 is bonded. It means a ring formed by a carbon atom in the skeleton and one or more arbitrary elements.
  • R 921 and R 922 form a ring Q A
  • the carbon atom of the anthracene skeleton to which R 921 is bonded the carbon atom of the anthracene skeleton to which R 922 is bonded, and four carbon atoms.
  • R 921 and R 922 form a monocyclic unsaturated ring
  • the ring formed by R 921 and R 922 is a benzene ring.
  • the "arbitrary element” is preferably at least one element selected from the group consisting of carbon element, nitrogen element, oxygen element, and sulfur element, unless otherwise specified in this specification.
  • a bond that does not form a ring may be terminated with a hydrogen atom or the like, or may be substituted with an "arbitrary substituent” described below.
  • the ring formed is a heterocycle.
  • the number of "one or more arbitrary elements" constituting a monocyclic or condensed ring is preferably 2 to 15, more preferably 3 to 12. , more preferably 3 or more and 5 or less.
  • a “monocycle” is preferred among “monocycle” and “fused ring.” Unless otherwise specified herein, the "unsaturated ring” is preferred between the “saturated ring” and the “unsaturated ring”. Unless otherwise stated herein, a “monocycle” is preferably a benzene ring. Unless otherwise stated herein, an “unsaturated ring” is preferably a benzene ring.
  • one or more pairs of two or more adjacent groups are “bonded with each other to form a substituted or unsubstituted monocycle” or “bonded with each other to form a substituted or unsubstituted fused ring”
  • one or more of the pairs of two or more adjacent atoms are bonded to each other to form a bond with a plurality of atoms of the parent skeleton and one or more of the 15 or more atoms.
  • a substituted or unsubstituted "unsaturated ring” is formed with at least one element selected from the group consisting of the following carbon elements, nitrogen elements, oxygen elements, and sulfur elements.
  • the substituent is, for example, the "arbitrary substituent” described below.
  • Specific examples of the substituent in the case where the above-mentioned “single ring” or “fused ring” has a substituent are the substituents described in the section of "Substituent described herein” above.
  • the substituent is, for example, the "arbitrary substituent” described below.
  • substituents in the case where the above-mentioned "single ring” or “fused ring” has a substituent are the substituents described in the section of "Substituent described herein" above. The above applies to cases in which "one or more sets of two or more adjacent groups combine with each other to form a substituted or unsubstituted monocycle" and "one or more sets of two or more adjacent groups” are combined with each other to form a substituted or unsubstituted condensed ring ("the case where they are combined to form a ring").
  • the substituent in the case of "substituted or unsubstituted” is, for example, an unsubstituted alkyl group having 1 to 50 carbon atoms, unsubstituted alkenyl group having 2 to 50 carbon atoms, unsubstituted alkynyl group having 2 to 50 carbon atoms, an unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, -Si(R 901 )(R 902 )(R 903 ), -O-(R 904 ), -S- (R 905 ), -N(R 906 )(R 907 ), Halogen atom, cyano group, nitro group, A group selected from the group consisting of an unsubstituted aryl group having 6 to 50 ring
  • R 901s When two or more R 901s exist, the two or more R 901s are the same or different, When two or more R 902s exist, the two or more R 902s are the same or different, When two or more R 903s exist, the two or more R 903s are the same or different, When two or more R 904s exist, the two or more R 904s are the same or different, When two or more R 905s exist, the two or more R 905s are the same or different, When two or more R 906s exist, the two or more R 906s are the same or different, When two or more R 907s exist, the two or more R 907s are the same or different.
  • the substituent in the case of "substituted or unsubstituted” is an alkyl group having 1 to 50 carbon atoms, A group selected from the group consisting of an aryl group having 6 to 50 ring carbon atoms and a heterocyclic group having 5 to 50 ring atoms.
  • the substituent in the case of "substituted or unsubstituted” is an alkyl group having 1 to 18 carbon atoms, A group selected from the group consisting of an aryl group having 6 to 18 ring carbon atoms and a heterocyclic group having 5 to 18 ring atoms.
  • any adjacent substituents may form a "saturated ring" or "unsaturated ring", preferably a substituted or unsubstituted saturated ring. Forms a membered ring, a substituted or unsubstituted saturated 6-membered ring, a substituted or unsubstituted unsaturated 5-membered ring, or a substituted or unsubstituted unsaturated 6-membered ring, more preferably a benzene ring do.
  • any substituent may further have a substituent.
  • the substituents that the arbitrary substituents further have are the same as the above arbitrary substituents.
  • the numerical range expressed using "AA-BB” has the numerical value AA written before “AA-BB” as the lower limit, and the numerical value BB written after "AA-BB”. means a range that includes as an upper limit value.
  • invention compounds The compounds of the present invention will be explained below.
  • the compound of the present invention is represented by the above formula (1).
  • equation (1) and symbols included in equation (1) and included in each equation described below will be explained. Unless otherwise specified, identical symbols have the same meaning.
  • the compounds of the present invention represented by formula (1) and the formulas included in formula (1) described below may be referred to as "invention compounds.”
  • N * is the central nitrogen atom.
  • R a and R b is a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, preferably 1 to 18 carbon atoms, more preferably 1 to 10 carbon atoms, and still more preferably 1 to 6 carbon atoms; Substituted aryl group having 6 to 30 ring carbon atoms, preferably 6 to 25, more preferably 6 to 12 ring atoms, or substituted or unsubstituted aryl group having 5 to 30 ring atoms, preferably 5 to 18, more preferably 5 ⁇ 13 heterocyclic groups. However, R a and R b may be combined with each other to form a substituted or unsubstituted ring.
  • one of R a and R b is a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, and the other is a substituted or aryl group having 6 to 30 ring carbon atoms.
  • one of R a and R b is a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms, and the other is more preferably a substituted or unsubstituted phenyl group.
  • the unsubstituted alkyl group having 1 to 30 carbon atoms represented by R a and R b is, for example, a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a s-butyl group, t-butyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, undecyl group, or dodecyl group, preferably methyl group, ethyl group, n-propyl group, isopropyl group, n -butyl group, isobutyl group, s-butyl group, t-butyl group, or pentyl group, more preferably methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl
  • the unsubstituted aryl group having 6 to 30 ring carbon atoms represented by R a and R b is, for example, a phenyl group, a biphenylyl group, a terphenylyl group, a biphenylenyl group, a naphthyl group, an anthryl group, a benzanthryl group, a phenanthryl group.
  • benzophenanthryl group phenalenyl group, picenyl group, pentaphenyl group, pyrenyl group, chrysenyl group, benzochrysenyl group, fluorenyl group, fluoranthenyl group, perylenyl group, or triphenylenyl group, preferably phenyl group, biphenylyl group.
  • terphenylyl group or naphthyl group, more preferably phenyl group, 2-, 3-, or 4-biphenylyl group, 2-, 3-, or 4-o-terphenylyl group, 2-, 3- , or 4-m-terphenylyl group, 2-, 3-, or 4-p-terphenylyl group, or 1- or 2-naphthyl group, more preferably phenyl group, 2-, 3-, or 4 -biphenylyl group or 1- or 2-naphthyl group, particularly preferably phenyl group.
  • the unsubstituted aromatic heterocyclic group having 5 to 30 ring atoms represented by R a and R b is, for example, a pyrrolyl group, a furyl group, a thienyl group, a pyridyl group, an imidazopyridyl group, a pyridazinyl group, a pyrimidinyl group, Pyrazinyl group, triazinyl group, imidazolyl group, oxazolyl group, thiazolyl group, pyrazolyl group, isoxazolyl group, isothiazolyl group, oxadiazolyl group, thiadiazolyl group, triazolyl group, tetrazolyl group, indolyl group, isoindolyl group, indolizinyl group, quinolidinyl group, quinolyl group , isoquinolyl group, cinnolyl group, phthalazinyl
  • the unsubstituted monocycle formed by R a and R b is, for example, a benzene ring, a cyclopentane ring, or a cyclohexane ring.
  • the unsubstituted condensed ring formed by R a and R b is, for example, a naphthalene ring or an anthracene ring.
  • R a and R b combine with each other to form an unsubstituted monocyclic ring or an unsubstituted fused ring
  • R a and R b form a ring together with the fluorene skeleton to which they are bonded, and the spiro It may form a ring.
  • the spiro ring is a hydrocarbon ring or a heterocycle, and is selected from a monocyclic ring, a fused ring, a bridged bicyclo ring, and a bridged tricyclo ring. Examples of substituted or unsubstituted spiro rings are shown below, but the invention is not limited thereto. * indicates the bonding position of the fluorene skeleton to the benzene ring.
  • R a and R b preferably do not combine with each other to form a substituted or unsubstituted ring.
  • R 2 , R 3 , R 6 and R 7 is a single bond that is bonded to *1, and R that is not a single bond that is bonded to R 1 , R 4 , R 5 , R 8 and *1 2 , R 3 , R 6 and R 7 are each independently a hydrogen atom, a substituted or unsubstituted carbon number of 1 to 30, preferably 1 to 18, more preferably 1 to 10, still more preferably 1 to 6 an alkyl group, a substituted or unsubstituted cycloalkyl group having 3 to 15, preferably 3 to 10, more preferably 3 to 6 ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms, or a substituted or unsubstituted heterocyclic group having 5 to 13 ring atoms.
  • R 1 , R 4 , R 5 , R 8 , and two adjacent ones selected from R 2 , R 3 , R 6 and R 7 that are not single bonds do not
  • R 2 or R 7 is preferably a single bond bonded to *1.
  • An unsubstituted cycloalkyl group having 3 to 15 ring carbon atoms represented by R 1 , R 4 , R 5 , R 8 and R 2 , R 3 , R 6 and R 7 which are not single bonds bonded to *1 is, for example, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, or a cyclooctyl group, preferably a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, or a cyclohexyl group.
  • R 1 , R 4 , R 5 , R 8 , and R 2 , R 3 , R 6 and R 7 which are not single bonds bonded to *1 represent an unsubstituted aryl group having 6 to 12 ring carbon atoms; The details are as described for R a and R b except that the number of ring carbon atoms is 6 to 12.
  • R 1 , R 4 , R 5 , R 8 and R 2 , R 3 , R 6 and R 7 that are not single bonds bonded to *1 may all be hydrogen atoms.
  • R 11 to R 14 are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, preferably 1 to 18 carbon atoms, more preferably 1 to 10 carbon atoms, even more preferably 1 to 6 carbon atoms, or It is a substituted or unsubstituted aryl group having 6 to 18 ring carbon atoms, preferably 6 to 12 carbon atoms. Two adjacent ones selected from R 11 to R 14 do not bond to each other and therefore do not form a ring.
  • All of R 11 to R 14 may be hydrogen atoms.
  • L 1 to L 4 are each independently a single bond or an arylene group having 6 to 30, preferably 6 to 25, more preferably 6 to 12 ring carbon atoms.
  • L 1 and L 2 are preferably each independently a single bond or an arylene group having 6 to 12 ring carbon atoms.
  • L 1 may be a single bond
  • L 2 may be a single bond.
  • L 3 is preferably a single bond.
  • L 4 is preferably a single bond.
  • L 3 and L 4 are preferably single bonds.
  • the unsubstituted arylene group having 6 to 30 ring carbon atoms represented by L 1 to L 4 above is 2 which is obtained by removing one hydrogen atom from an unsubstituted aryl group having 6 to 30 ring carbon atoms. It is the basis of valence. Details of the unsubstituted aryl group having 6 to 30 ring carbon atoms are as described for R a and R b .
  • Ar 1 and Ar 2 are groups represented by any of the following formulas (1a) to (1g).
  • *21 is the bonding position to L 1 or L 2 .
  • One selected from R 101 to R 105 is a single bond bonded to *22, and one selected from R 106 to R 110 is a single bond bonded to *23, selected from R 111 to R 115 .
  • Each of R 101 to R 115 that is not a single bond is independently a hydrogen atom, an unsubstituted alkyl group having 1 to 10 carbon atoms, or an unsubstituted aryl group having 6 to 12 ring carbon atoms.
  • the two adjacent ones selected from R 101 to R 105 that are not single bonds do not bond to each other and therefore do not form a ring
  • the two adjacent ones selected from R 106 to R 110 that are not single bonds do not bond to each other and therefore do not form a ring
  • Two adjacent ones selected from R 111 to R 115 that are not single bonds do not bond to each other and therefore do not form a ring.
  • R 101 to R 115 The details of the unsubstituted aryl group having 6 to 12 ring carbon atoms represented by R 101 to R 115 are as described for R a and R b except that the ring carbon number is 6 to 12. .
  • All of R 101 to R 105 that are not single bonds bonded to *22 may be hydrogen atoms, and all of R 106 to R 110 that are not single bonds bonded to *23 may be hydrogen atoms, All of R 111 to R 115 that are not single bonds bonded to *24 may be hydrogen atoms.
  • n is 0 or 1
  • l is 0 or 1.
  • *22 represents the bonding position to L 1 or L 2 (*22 represents *21)
  • m is 0, n is 0, and l is 1
  • *23 represents the bonding position to L 1 or L 2 (*23 represents *21)
  • *24 is L 1 or L 2 represents the bonding position to (*24 represents *21).
  • m is 0, n is 0, and l is 0.
  • *24 represents *21, and formula (1a) is expressed by the following formula.
  • n is 1
  • l is 0.
  • *22 represents *21
  • *24 represents *23
  • formula (1a) is represented by the following formula.
  • n is 0, and l is 1.
  • *23 represents *21
  • formula (1a) is represented by the following formula.
  • m is 1, n is 1, and l is 0.
  • *24 represents *23
  • formula (1a) is expressed by the following formula.
  • n is 0, and l is 1.
  • *23 represents *22
  • formula (1a) is expressed by the following formula.
  • n is 1
  • l is 1.
  • *22 represents *21
  • formula (1a) is represented by the following formula.
  • formula (1a) is expressed by the following formula.
  • the group represented by formula (1a) preferably satisfies at least one of the following (i) to (iii). (i) R 101 or R 105 is a single bond bonded to *22 (ii) R 106 or R 110 is a single bond bonded to *23 (iii) R 111 or R 115 is bonded to *24 is a single bond
  • R 116 to R 120 are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms, or a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms; is a heterocyclic group having 5 to 13 ring atoms. Two adjacent ones selected from R 116 to R 120 do not bond to each other and therefore do not form a ring.
  • All of R 116 to R 120 may be hydrogen atoms.
  • the group represented by formula (1a) is preferably represented by the following formula.
  • R is omitted for simplification.
  • Formula (1b) is represented by the following formula.
  • L 1 is a p-phenylene group and Ar 1 is represented by formula (1b)
  • One selected from 125 and R 128 is a single bond bonded to *26
  • L 2 is a p-phenylene group and Ar 2 is represented by formula (1b)
  • R 128 is a single bond bonded to *26.
  • R 121 is preferably a single bond bonded to *26, and in another embodiment, R 122 is preferably a single bond bonded to *26. All of R 121 to R 128 that are not single bonds bonded to *26 may be hydrogen atoms.
  • Formula (1c) is represented by the following formula.
  • *27 is the bonding position to L 1 or L 2 .
  • R 131 to R 140 is a single bond bonded to *28.
  • R 131 to R 140 which are not single bonds are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms, preferably 1 to 6 carbon atoms, or a substituted or unsubstituted ring-forming carbon number group. It is 6 to 12 aryl groups. Two adjacent ones selected from R 131 to R 140 that are not single bonds do not bond to each other and therefore do not form a ring.
  • R 131 to R 140 The details of the unsubstituted alkyl group having 1 to 6 carbon atoms represented by R 131 to R 140 are as described for R a and R b except that the number of carbon atoms is 1 to 6. Details of the unsubstituted aryl group having 6 to 12 ring carbon atoms represented by R 131 to R 140 are as described for R a and R b except that the ring carbon number is 6 to 12. .
  • R 131 is preferably a single bond
  • R 132 is preferably a single bond
  • R 140 is a single bond bonded to *28. All of R 131 to R 140 that are not single bonds bonded to *28 may be hydrogen atoms.
  • Formula (1d) is represented by the following formula.
  • *29 is the bonding position to L 1 or L 2 .
  • R 141 to R 152 is a single bond bonded to *30.
  • R 141 to R 152 which are not single bonds are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms, preferably 1 to 6 carbon atoms, or a substituted or unsubstituted ring-forming carbon number group. It is 6 to 12 aryl groups. Two adjacent ones selected from R 141 to R 152 that are not single bonds do not bond to each other and therefore do not form a ring structure.
  • R 141 to R 152 Details of the unsubstituted alkyl group having 1 to 10 carbon atoms represented by R 141 to R 152 are as described for R a and R b except that the number of carbon atoms is 1 to 10.
  • the details of the unsubstituted aryl group having 6 to 12 carbon atoms in the ring represented by R 141 to R 152 are as described for R a and R b except that the number of carbon atoms in the ring is 6 to 12. .
  • All of R 141 to R 152 that are not single bonds bonded to *30 may be hydrogen atoms.
  • Formula (1e) is represented by the following formula.
  • *31 is the bonding position to L 1 or L 2 .
  • One selected from R 161 to R 165 is a single bond bonded to *32, and the other selected from R 161 to R 165 is a single bond bonded to *33.
  • R 161 to R 165 which are neither a single bond bonded to *32 nor a single bond bonded to *33 are each independently a hydrogen atom, an unsubstituted carbon number of 1 to 10, preferably 1 to 6 is an alkyl group or an unsubstituted phenyl group.
  • Two adjacent ones selected from R 161 to R 165 that are neither a single bond bonded to *32 nor a single bond bonded to *33 do not bond to each other and therefore do not form a ring.
  • R 161 to R 165 The details of the unsubstituted alkyl group having 1 to 10 carbon atoms represented by R 161 to R 165 which are neither a single bond bonded to *32 nor a single bond bonded to *33 are as follows: As described for R a and R b except for the following.
  • the details of the unsubstituted aryl group having 6 to 12 carbon atoms in the ring represented by R 141 to R 152 are as described for R a and R b except that the number of carbon atoms in the ring is 6 to 12. .
  • All of R 161 to R 165 which are neither the single bond bonded to *32 nor the single bond bonded to *33, may be hydrogen atoms.
  • R 171 to R 175 and R 181 to R 185 are each independently a hydrogen atom or an unsubstituted alkyl group having 1 to 10 carbon atoms, preferably 1 to 6 carbon atoms.
  • Two adjacent ones selected from R 171 to R 175 may be bonded to each other to form one or more unsubstituted benzene rings, or may not be bonded to each other and therefore do not form a ring
  • Two adjacent ones selected from R 181 to R 185 may be bonded to each other to form one or more unsubstituted benzene rings, or may not be bonded to each other and therefore do not form a ring.
  • R 171 to R 175 and R 181 to R 185 Details of the unsubstituted alkyl group having 1 to 10 carbon atoms represented by R 171 to R 175 and R 181 to R 185 are as described for R a and R b except that the number of carbon atoms is 1 to 10. It is. All of R 171 to R 175 and R 181 to R 185 may be hydrogen atoms.
  • Formula (1e) includes groups represented by the following formulas (1e-1) to (1e-5), with formulas (1e-1), (1e-2) or (1e-4) being preferred.
  • *34 is the bonding position to L 1 or L 2 .
  • X is an oxygen atom, a sulfur atom, or NRA .
  • X is preferably an oxygen atom or NRA .
  • R 191 to R 198 and R A is a single bond bonded to *35.
  • the R A that is not a single bond is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms.
  • R 191 to R 198 that are not single bonds are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 ring-forming carbon atoms, or a substituted or unsubstituted heterocyclic group having 5 to 13 ring atoms.
  • Two adjacent ones selected from R 191 to R 198 that are not single bonds may be bonded to each other to form one or more unsubstituted benzene rings, or may not be bonded to each other and therefore form a ring. You don't have to.
  • the details of the unsubstituted heterocyclic group having 5 to 13 ring atoms represented by R 191 to R 198 that are not single bonds are as follows with respect to R a and R b except that the number of ring atoms is 5 to 13. As described.
  • R 191 to R 198 that are not single bonds bonded to 35 may be hydrogen atoms.
  • R 191 to R 194 When X is an oxygen atom or a sulfur atom, preferably one selected from R 191 to R 194 is a single bond bonded to *35.
  • X is NR A , preferably one selected from R 191 to R 194 and R A is a single bond bonded to *35. It is particularly preferable that R A is a single bond bonded to *35 or an unsubstituted phenyl group.
  • Formula (1g) is represented by the following formula.
  • *36 is the bonding position to L 1 or L 2 .
  • R B , R C , and R 201 to R 208 is a single bond bonded to *37.
  • R B and R C which are not single bonds are each independently a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms, or a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms; It is an unsubstituted heterocyclic group having 5 to 13 ring atoms.
  • R B and R C which are not single bonds, may be bonded to each other to form a substituted or unsubstituted ring.
  • R B and R C are preferably each independently a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a phenyl group.
  • the details of the unsubstituted alkyl group having 1 to 6 carbon atoms represented by R B and R C which are not single bonds are as described for R a and R b except that the number of carbon atoms is 1 to 6. .
  • the details of the unsubstituted aryl group having 6 to 12 ring carbon atoms represented by R B and R C that are not single bonds are described with respect to R a and R b except that the ring carbon number is 6 to 12.
  • Details of the unsubstituted heterocyclic group having 5 to 13 ring atoms represented by R B and R C which are not single bonds are described with respect to R a and R b except that the number of ring atoms is 5 to 13.
  • Details of the unsubstituted ring formed by bonding R B and R C , which are not single bonds, to each other are as described for R a and R b .
  • R 201 to R 208 which are not single bonds are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 ring carbon atoms, or a substituted or unsubstituted heterocyclic group having 5 to 13 ring atoms.
  • two adjacent ones selected from R 201 to R 208 that are not single bonds do not bond to each other and therefore do not form a ring.
  • R 202 or R 207 is preferably a single bond bonded to *37.
  • At least one of Ar 1 and Ar 2 is preferably a group represented by the above formula (1a) or (1g).
  • Ar 1 or Ar 2 is a group represented by the above formula (1a), and the group represented by the formula (1a) is one of the following (i) to (iii). It is preferable that at least one condition is satisfied.
  • R 101 or R 105 is a single bond bonded to *22
  • R 106 or R 110 is a single bond bonded to *23
  • R 111 or R 115 is bonded to *24 is a single bond
  • Ar 1 or Ar 2 is a group represented by the above formula (1g), and in the group represented by the formula (1g), R B and R C are each independently Preferably, it is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or a substituted or unsubstituted phenyl group.
  • Ar 1 or Ar 2 is a group represented by the above formula (1g), and in the group represented by the formula (1g), R 202 or R 207 is bonded to *37. A single bond is preferable.
  • hydrogen atom as used herein includes light hydrogen atoms, deuterium atoms, and tritium atoms. Accordingly, the compounds of the invention may contain naturally occurring deuterium atoms. Further, a deuterium atom may be intentionally introduced into compound (1) by using a deuterated compound as part or all of the raw material compound. Therefore, in one embodiment of the present invention, compound (1) contains at least one deuterium atom. That is, the invention compound may be a compound represented by formula (1), in which at least one of the hydrogen atoms contained in the compound is a deuterium atom.
  • At least one hydrogen atom selected from the following hydrogen atoms may be a deuterium atom.
  • “substituted or unsubstituted” the number of carbon atoms, and the number of atoms are omitted.
  • R a and R b of formula (1) are an alkyl group, an aryl group, or a heterocyclic group, the hydrogen atoms they have; A hydrogen atom represented by R 1 to R 5 , R 8 , and R 6 and R 7 which are not single bonds bonded to *1 in formula (1); When R 1 to R 5 , R 8 , and R 6 and R 7 that are not single bonds bonded to *1 in formula (1) are an alkyl group, a cycloalkyl group, an aryl group, or a heterocyclic group, these are hydrogen atom; Hydrogen atoms represented by R 11 to R 14 of formula (1); When R 11 to R 14 of formula (1) are an alkyl group or an aryl group, a hydrogen atom possessed by these; When L 1 to L 4 of formula (1) are arylene groups, hydrogen atoms possessed by these; In formula (1a), R 101 to R 105 that are not a single bond bonded to * 22, R 106 to R 110 that are not a single bond bonded
  • the deuteration rate of the invention compound depends on the deuteration rate of the raw material compound used. Even if a raw material with a predetermined deuteration rate is used, a certain proportion of naturally derived light hydrogen isotopes may be included. Therefore, the aspect of the deuteration rate of the invention compound shown below is the ratio calculated by simply counting the number of deuterium atoms represented by the chemical formula, but the ratio takes into account trace amounts of naturally occurring isotopes. included.
  • the deuteration rate of the invention compound is preferably 1% or more, more preferably 3% or more, even more preferably 5% or more, even more preferably 10% or more, even more preferably 50% or more.
  • the invention compound may be a mixture containing a deuterated compound and a non-deuterated compound, or a mixture of two or more compounds having different deuteration rates.
  • the deuteration rate of such a mixture is preferably 1% or more, more preferably 3% or more, even more preferably 5% or more, even more preferably 10% or more, even more preferably 50% or more, and 100% or more. less than %.
  • the ratio of the number of deuterium atoms to the total number of hydrogen atoms in the invention compound is preferably 1% or more, more preferably 3% or more, even more preferably 5% or more, even more preferably 10% or more, and 100% or more. % or less.
  • substituted XX group included in the definitions of the above formulas is a substituted XX group
  • the details of the substituent are as described in "Substituents in the case of "substituted or unsubstituted””. and is preferably an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 12 ring atoms, or an aromatic heterocyclic group having 5 to 13 ring atoms, more preferably 1 to 6 carbon atoms. is an alkyl group or an aryl group having 6 to 12 ring carbon atoms. Details of each group are as described above.
  • the compounds of the invention can be easily produced by those skilled in the art with reference to the following synthesis examples and known synthesis methods.
  • the invention compound is preferably a material for a hole transport zone or a light emitting layer of a fluorescent or phosphorescent EL device, more preferably a material for a hole transport zone, and even more preferably a hole injection layer, a hole transport layer, an electron blocking layer, or an excitation layer. It is used as a material for a child blocking layer, particularly preferably a hole injection layer or a hole transport layer.
  • the organic EL device of the present invention may be a monochromatic fluorescent or phosphorescent type light emitting device, a fluorescent/phosphorescent hybrid type white light emitting device, or a simple type having a single light emitting unit.
  • the device may be of a tandem type having a plurality of light emitting units, and is preferably a fluorescent light emitting device.
  • the "light-emitting unit” refers to a minimum unit that includes an organic layer, at least one of which is a light-emitting layer, and emits light by recombining injected holes and electrons.
  • the light-emitting unit may be a multilayer type having a plurality of phosphorescence-emitting layers or fluorescent light-emitting layers.
  • a space layer may be provided for the purpose of preventing excitons from diffusing into the fluorescent light emitting layer.
  • a typical layer structure of a simple light emitting unit is shown below. The layers in parentheses are optional.
  • Each of the phosphorescent or fluorescent light-emitting layers may emit light of a different color from each other.
  • the light emitting unit (f) hole injection layer/) hole transport layer/first phosphorescent layer (red light emitting layer)/second phosphorescent light emitting layer (green light emitting layer)/space layer/fluorescent light emitting layer.
  • Examples include a layer structure such as a layer (blue light emitting)/electron transport layer.
  • an electron blocking layer may be provided between each light emitting layer and the hole transport layer or space layer, as appropriate.
  • a hole blocking layer may be provided between each light emitting layer and the electron transport layer as appropriate.
  • Typical device configurations of tandem type organic EL devices include the following device configurations.
  • the first light emitting unit and the second light emitting unit can be independently selected from the above light emitting units, for example.
  • the intermediate layer is generally also called an intermediate electrode, intermediate conductive layer, charge generation layer, electron extraction layer, connection layer, or intermediate insulating layer, and supplies electrons to the first light emitting unit and holes to the second light emitting unit. Any known material configuration can be used.
  • an electron blocking layer (not shown) may be provided on the anode 3 side of the light emitting layer 5, and a hole blocking layer (not shown) may be provided on the cathode 4 side of the light emitting layer 5.
  • FIG. 3 is a schematic diagram showing another configuration of the organic EL element of the present invention.
  • the organic EL element 12 includes a substrate 2, an anode 3, a cathode 4, and a light emitting unit 30 disposed between the anode 3 and the cathode 4.
  • the light emitting unit 30 has a light emitting layer 5.
  • the hole transport zone arranged between the anode 3 and the light emitting layer 5 is formed from a hole injection layer 6a, a first hole transport layer 6b, a second hole transport layer 6c, and a third hole transport layer 6d. has been done.
  • the electron transport zone arranged between the light emitting layer 5 and the cathode 4 is formed from the first electron transport layer 7a and the second electron transport layer 7b.
  • a host combined with a fluorescent dopant material is referred to as a fluorescent host
  • a host combined with a phosphorescent dopant material is referred to as a phosphorescent host.
  • Fluorescent hosts and phosphorescent hosts are not distinguished only by molecular structure. That is, the phosphorescent host refers to a material containing a phosphorescent dopant that forms a phosphorescent layer, and does not mean that it cannot be used as a material to form a fluorescent layer. The same applies to fluorescent hosts.
  • the substrate is used as a support for the organic EL element.
  • a plate of glass, quartz, plastic, etc. can be used.
  • a flexible substrate may be used.
  • the flexible substrate include plastic substrates made of polycarbonate, polyarylate, polyethersulfone, polypropylene, polyester, polyvinyl fluoride, and polyvinyl chloride.
  • an inorganic vapor-deposited film can also be used.
  • Anode It is preferable to use a metal, an alloy, an electrically conductive compound, a mixture thereof, or the like having a large work function (specifically, 4.0 eV or more) for the anode formed on the substrate.
  • a metal, an alloy, an electrically conductive compound, a mixture thereof, or the like having a large work function (specifically, 4.0 eV or more) for the anode formed on the substrate.
  • ITO indium oxide-tin oxide
  • indium oxide-tin oxide containing silicon or silicon oxide indium oxide-zinc oxide
  • indium oxide containing tungsten oxide and zinc oxide examples include graphene.
  • gold Au
  • platinum Pt
  • nickel Ni
  • tungsten W
  • Cr chromium
  • Mo molybdenum
  • iron Fe
  • Co cobalt
  • Cu copper
  • palladium Pd
  • titanium Ti
  • nitrides of the above metals eg, titanium nitride
  • These materials are usually deposited using a sputtering method.
  • a sputtering method For example, for indium oxide-zinc oxide, use a target in which 1 to 10 wt% of zinc oxide is added to indium oxide, and for indium oxide containing tungsten oxide and zinc oxide, 0.5 to 5 wt% of tungsten oxide is added to indium oxide. %, and by using a target containing 0.1 to 1 wt % zinc oxide, it can be formed by a sputtering method. In addition, it may be produced by a vacuum evaporation method, a coating method, an inkjet method, a spin coating method, or the like.
  • the hole injection layer formed in contact with the anode is formed using a material that can easily inject holes regardless of the work function of the anode. , alloys, electrically conductive compounds, mixtures thereof, and elements belonging to Group 1 or Group 2 of the Periodic Table of Elements). Elements belonging to Group 1 or Group 2 of the periodic table of elements, which are materials with a small work function, such as alkali metals such as lithium (Li) and cesium (Cs), as well as magnesium (Mg), calcium (Ca), and strontium.
  • Alkaline earth metals such as (Sr), alloys containing these (for example, MgAg, AlLi), rare earth metals such as europium (Eu), ytterbium (Yb), alloys containing these, etc. can also be used.
  • a vacuum evaporation method or a sputtering method can be used.
  • silver paste or the like a coating method, an inkjet method, etc. can be used.
  • Hole injection layer is a layer containing a material with high hole injection property (hole injection material), and is located between the anode and the light emitting layer or, if present, with the hole transport layer. Formed between the anodes.
  • Hole-injecting materials other than the invention compounds include molybdenum oxide, titanium oxide, vanadium oxide, rhenium oxide, ruthenium oxide, chromium oxide, zirconium oxide, hafnium oxide, tantalum oxide, and silver oxide. oxide, tungsten oxide, manganese oxide, etc. can be used.
  • High molecular compounds oligomers, dendrimers, polymers, etc.
  • PVK poly(N-vinylcarbazole)
  • PVTPA poly(4-vinyltriphenylamine)
  • PTPDMA poly[N-(4- ⁇ N'-[4-(4-diphenylamino) phenyl]phenyl-N'-phenylamino ⁇ phenyl) methacrylamide]
  • PTPDMA poly[N,N'-bis(4-butylphenyl)-N,N'-bis(phenyl)benzidine]
  • Polymer compounds such as Poly-TPD
  • a polymer compound to which an acid is added such as poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonic acid) (PEDOT/PSS) or polyaniline/poly(styrene sulfonic acid) (PAni/PSS), is used. You can also do that.
  • R 221 to R 226 are each independently a cyano group, -CONH 2 , a carboxyl group, or -COOR 227 (R 227 is an alkyl group having 1 to 20 carbon atoms or a cycloalkyl group having 3 to 20 carbon atoms)
  • R 227 is an alkyl group having 1 to 20 carbon atoms or a cycloalkyl group having 3 to 20 carbon atoms
  • two adjacent groups selected from R 221 and R 222 , R 223 and R 224 , and R 225 and R 226 bond to each other to form a group represented by -CO-O-CO-.
  • R 227 examples include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, t-butyl group, cyclopentyl group, and cyclohexyl group.
  • the hole transport layer is a layer containing a material with high hole transport properties (hole transport material), and is located between the anode and the light emitting layer or, if present, between the hole injection layer and the hole transport layer. It is formed between the light emitting layers.
  • the compounds of the invention may be used alone or in combination with the compounds listed below in the hole transport layer.
  • the hole transport layer may have a single layer structure or a multilayer structure including two or more layers.
  • the hole transport layer may have a two-layer structure including a first hole transport layer (on the anode side) and a second hole transport layer (on the cathode side). That is, the hole transport zone may include a first hole transport layer on the anode side and a second hole transport layer on the cathode side.
  • the hole transport layer may have a three-layer structure including, in order from the anode side, a first hole transport layer, a second hole transport layer, and a third hole transport layer. That is, the third hole transport layer may be arranged between the second hole transport layer and the light emitting layer.
  • the single-layer structure hole transport layer is preferably adjacent to the light emitting layer, and the hole transport layer closest to the cathode in the multilayer structure is, for example, the two-layer structure
  • the second hole transport layer and the third hole transport layer of the three-layer structure are preferably adjacent to the light emitting layer.
  • the below-mentioned electron A blocking layer or the like may be interposed.
  • the hole transport layer has a two-layer structure
  • at least one of the first hole transport layer and the second hole transport layer contains the invention compound. That is, the invention compound is contained only in the first hole transport layer, only in the second hole transport layer, or in both the first hole transport layer and the second hole transport layer.
  • the inventive compound is preferably included in the second hole transport layer. That is, it is preferable that the invention compound is contained only in the second hole transport layer, or that the invention compound is contained in the first hole transport layer and the second hole transport layer.
  • the hole transport layer has a three-layer structure
  • at least one of the first to third hole transport layers contains the invention compound. That is, the inventive compound is present in only one layer selected from the first to third hole transport layers (only the first hole transport layer, only the second hole transport layer, or only the third hole transport layer), the first to the third hole transport layers.
  • the inventive compound is preferably included in the third hole transport layer. That is, it is preferable that the invention compound is contained only in the third hole transport layer, or that the invention compound is contained in the third hole transport layer and one or both of the first hole transport layer and the second hole transport layer. .
  • the invention compound contained in each of the hole transport layers is preferably a light hydrogen compound from the viewpoint of manufacturing cost.
  • the light hydrogen compound refers to an invention compound in which all hydrogen atoms are light hydrogen atoms. Therefore, in the present invention, one or both of the first hole transport layer and the second hole transport layer (in the case of a two-layer structure), and at least one of the first to third hole transport layers are made substantially of light hydrogen. It includes an organic EL device containing an inventive compound consisting only of organic EL elements. "Invention compound consisting essentially only of light hydrogen bodies” means that the content ratio of light hydrogen bodies to the total amount of the invention compounds is 90 mol% or more, preferably 95 mol% or more, more preferably 99 mol% or more (each (including 100%).
  • aromatic amine compounds for example, aromatic amine compounds, carbazole derivatives, anthracene derivatives, etc. can be used.
  • aromatic amine compounds include 4,4'-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (abbreviation: NPB) and N,N'-bis(3-methylphenyl)-N , N'-diphenyl-[1,1'-biphenyl]-4,4'-diamine (abbreviation: TPD), 4-phenyl-4'-(9-phenylfluoren-9-yl)triphenylamine (abbreviation: BAFLP), 4,4'-bis[N-(9,9-dimethylfluoren-2-yl)-N-phenylamino]biphenyl (abbreviation: DFLDPBi), 4,4',4''-tris(N,N -diphenylamino)triphen
  • carbazole derivatives examples include 4,4'-di(9-carbazolyl)biphenyl (abbreviation: CBP), 9-[4-(9-carbazolyl)phenyl]-10-phenylanthracene (abbreviation: CzPA), and Examples include 9-phenyl-3-[4-(10-phenyl-9-anthryl)phenyl]-9H-carbazole (abbreviation: PCzPA).
  • anthracene derivatives examples include 2-t-butyl-9,10-di(2-naphthyl)anthracene (abbreviation: t-BuDNA), 9,10-di(2-naphthyl)anthracene (abbreviation: DNA), and , 9,10-diphenylanthracene (abbreviation: DPAnth).
  • Polymer compounds such as poly(N-vinylcarbazole) (abbreviation: PVK) and poly(4-vinyltriphenylamine) (abbreviation: PVTPA) can also be used.
  • PVK poly(N-vinylcarbazole)
  • PVTPA poly(4-vinyltriphenylamine)
  • compounds other than those mentioned above may be used as long as they have higher hole transport properties than electron transport properties.
  • the first hole transport layer contains one or more compounds represented by the following formula (11) or formula (12). is preferred.
  • one or both of the first hole transport layer and the second hole transport layer is 1 represented by the following formula (11) or (12). Preferably, it contains one or more compounds.
  • the organic EL device of the present invention having a hole transport layer with an n-layer structure n is an integer of 4 or more
  • at least one of the first hole transport layer to the (n-1)th hole transport layer has the following formula: It is preferable to contain one or more compounds represented by (11) or formula (12).
  • L A1 , L B1 , L C1 , L A2 , L B2 , L C2 and L D2 are each independently a single bond, a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms, or a substituted or unsubstituted arylene group is a divalent heterocyclic group having 5 to 50 ring atoms, k is 1, 2, 3 or 4, When k is 1, L E2 is a substituted or unsubstituted arylene group having 6 to 50 ring atoms, or a substituted or unsubstituted divalent heterocyclic group having 5 to 50 ring atoms; When k is 2, 3 or 4, 2, 3 or 4 L E2 are the same or different, When k is 2, 3 or 4, the plurality of L E2 's are bonded to each other to form a substituted or unsubstituted monocycle, bonded to each other to form a substituted or
  • a 1 , B 1 , C 1 , A 2 , B 2 , C 2 and D 2 are each independently a substituted or unsubstituted aryl group having 6 to 50 ring-forming carbon atoms, or a substituted or unsubstituted ring-forming aryl group
  • R' 901 , R' 902 and R' 903 are each independently a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms
  • A1, B1, C1, A2, B2, C2, and D2 are preferably each independently a substituted or unsubstituted phenylene group, a substituted or unsubstituted biphenyl group, Substituted or unsubstituted terphenyl group, substituted or unsubstituted naphthyl group, substituted or unsubstituted fluorenyl group, substituted or unsubstituted dibensofuranyl group, substituted or unsubstituted dibenzothiophenyl group, and substituted or unsubstituted dibenzothiophenyl group. selected from carbazolyl groups.
  • At least one of A1, B1, and C1, and in formula (12), at least one of A2, B2, C2, and D2 is substituted or unsubstituted biphenyl. group, substituted or unsubstituted terphenyl group, substituted or unsubstituted naphthyl group, substituted or unsubstituted fluorenyl group, substituted or unsubstituted dibensofuranyl group, or substituted or unsubstituted dibenzothiophenyl group, substituted or unsubstituted It is a substituted carbazolyl group.
  • the fluorenyl groups that A1, B1, C1, A2, B2, C2, and D2 can have may have a substituent at the 9-position, for example, 9,9-dimethylfluorenyl group, 9,9- It may also be a diphenylfluorenyl group. Further, the substituents at the 9-position may form a ring, for example, the substituents at the 9-position may form a fluorene skeleton or a xanthene skeleton.
  • L A1 , L B1 , L C1 , L A2 , L B2 , L C2 and L D2 are preferably each independently a single bond or a substituted or unsubstituted arylene group having 6 to 12 ring carbon atoms.
  • the light emitting layer is a layer containing a highly luminescent material (dopant material), and various materials can be used.
  • a fluorescent material or a phosphorescent material can be used as a dopant material.
  • Fluorescent materials are compounds that emit light from a singlet excited state
  • phosphorescent materials are compounds that emit light from a triplet excited state.
  • the light emitting layer is a single layer.
  • the light emitting layer includes a first light emitting layer and a second light emitting layer.
  • Pyrene derivatives, styrylamine derivatives, chrysene derivatives, fluoranthene derivatives, fluorene derivatives, diamine derivatives, triarylamine derivatives, etc. can be used as blue fluorescent materials that can be used in the light-emitting layer.
  • N,N'-bis[4-(9H-carbazol-9-yl)phenyl]-N,N'-diphenylstilbene-4,4'-diamine (abbreviation: YGA2S), 4-(9H -carbazol-9-yl)-4'-(10-phenyl-9-anthryl)triphenylamine (abbreviation: YGAPA), 4-(10-phenyl-9-anthryl)-4'-(9-phenyl-9H -carbazol-3-yl)triphenylamine (abbreviation: PCBAPA).
  • Aromatic amine derivatives and the like can be used as green fluorescent materials that can be used in the light emitting layer.
  • 2PCAPA N-(9,10-diphenyl-2-anthryl)-N,9-diphenyl-9H-carbazol-3-amine
  • 2PCABPhA N-[9,10-bis(1,1 '-biphenyl-2-yl)-2-anthryl]-N,9-diphenyl-9H-carbazol-3-amine
  • 2DPAPA N-(9,10-diphenyl-2-anthryl)-N,N ',N'-triphenyl-1,4-phenylenediamine
  • 2DPAPA N-[9,10-bis(1,1'-biphenyl-2-yl)-2-anthryl]-N,N' , N'-triphenyl-1,4-phenylenediamine
  • 2DPABPhA N-[9,10-bis(1,1'-biphenyl-2
  • Tetracene derivatives, diamine derivatives, etc. can be used as red fluorescent materials that can be used in the light emitting layer.
  • N,N,N',N'-tetrakis(4-methylphenyl)tetracene-5,11-diamine abbreviation: p-mPhTD
  • 7,14-diphenyl-N,N,N' examples include N'-tetrakis(4-methylphenyl)acenaphtho[1,2-a]fluoranthene-3,10-diamine (abbreviation: p-mPhAFD).
  • the light-emitting layer contains a fluorescent material (fluorescent dopant material).
  • Metal complexes such as iridium complexes, osmium complexes, and platinum complexes are used as blue-based phosphorescent materials that can be used in the light-emitting layer.
  • An iridium complex or the like is used as a green phosphorescent material that can be used in the light emitting layer.
  • Tris(2-phenylpyridinato-N,C2')iridium(III) (abbreviation: Ir(ppy)3), bis(2-phenylpyridinato-N,C2')iridium(III) acetylacetonate ( Abbreviation: Ir(ppy)2(acac)), bis(1,2-diphenyl-1H-benzimidazolato)iridium(III) acetylacetonate (abbreviation: Ir(pbi)2(acac)), bis(benzo[ h] quinolinato) iridium (III) acetylacetonate (abbreviation: Ir(bzz)2(acac)), and the like.
  • Metal complexes such as iridium complexes, platinum complexes, terbium complexes, and europium complexes are used as red-colored phosphorescent materials that can be used in the light-emitting layer.
  • bis[2-(2′-benzo[4,5- ⁇ ]thienyl)pyridinato-N,C3′]iridium(III) acetylacetonate abbreviation: Ir(btp)2(acac)
  • Bis(1-phenylisoquinolinato-N,C2')iridium(III) acetylacetonate abbreviation: Ir(piq)2(acac)
  • (acetylacetonato)bis[2,3-bis(4-fluoro) phenyl)quinoxalinato]iridium(III) abbreviation: Ir(Fdpq)2(acac)
  • tris(acetylacetonato)(monophenanthroline)terbium(III) (abbreviation: Tb(acac)3(Phen)
  • tris(1,3-diphenyl-1,3-propanedionato)(monophenanthroline) europium (III) (abbreviation: Eu(DBM)3(Phen)
  • tris[1-(2-thenoyl)-3,3,3-trifluoroacetonato](monophenanthroline) europium(III) (abbreviation: Eu( Rare earth metal complexes such as TTA)3(Phen) can be used as phosphorescent materials because they emit light from rare earth metal ions (electronic transition between different multiplicities).
  • the light emitting layer may have a structure in which the above-mentioned dopant material is dispersed in another material (host material). It is preferable to use a material that has a higher lowest unoccupied orbital level (LUMO level) and a lower highest occupied orbital level (HOMO level) than the dopant material.
  • LUMO level lowest unoccupied orbital level
  • HOMO level lowest occupied orbital level
  • host materials include (1) metal complexes such as aluminum complexes, beryllium complexes, or zinc complexes; (2) Heterocyclic compounds such as oxadiazole derivatives, benzimidazole derivatives, or phenanthroline derivatives, (3) fused aromatic compounds such as carbazole derivatives, anthracene derivatives, phenanthrene derivatives, pyrene derivatives, or chrysene derivatives, (4) Aromatic amine compounds such as triarylamine derivatives or fused polycyclic aromatic amine derivatives are used.
  • tris(8-quinolinolato)aluminum(III) (abbreviation: Alq)
  • tris(4-methyl-8-quinolinolato)aluminum(III) (abbreviation: Almq3)
  • bis(10-hydroxybenzo[h]quinolinato)beryllium (II) (abbreviation: BeBq2)
  • bis(2-methyl-8-quinolinolato)(4-phenylphenolato)aluminum(III) abbreviation: BAlq
  • bis(8-quinolinolato)zinc(II) (abbreviation: Znq)
  • bis[2-(2-benzoxazolyl)phenolato]zinc(II) (abbreviation: ZnPBO), bis[2-(2-benzothiazolyl)phenolato]zinc(II) (abbreviation: ZnBTZ), etc.
  • anthracene compound in the case of a blue fluorescent element, it is preferable to use the following anthracene compound as a host material.
  • the organic EL element when the light-emitting layer includes a first light-emitting layer and a second light-emitting layer, at least one of the components constituting the first light-emitting layer contains the second light-emitting layer. It is different from the constituent components.
  • the dopant material contained in the first light emitting layer may be different from the dopant material contained in the second light emitting layer, or the host material contained in the first light emitting layer may be different from the host material contained in the second light emitting layer. Different aspects are mentioned.
  • the light-emitting layer may contain a light-emitting compound (hereinafter sometimes simply referred to as a "fluorescent compound”) that exhibits fluorescent light emission with a main peak wavelength of 500 nm or less.
  • a light-emitting compound hereinafter sometimes simply referred to as a "fluorescent compound” that exhibits fluorescent light emission with a main peak wavelength of 500 nm or less.
  • the method for measuring the main peak wavelength of a compound is as follows. A 5 ⁇ mol/L toluene solution of the compound to be measured is prepared and placed in a quartz cell, and the emission spectrum (vertical axis: emission intensity, horizontal axis: wavelength) of this sample is measured at room temperature (300K). The emission spectrum can be measured using a spectrofluorometer (device name: F-7000) manufactured by Hitachi High-Tech Science Co., Ltd. Note that the emission spectrum measuring device is not limited to the device used here. In the emission spectrum, the peak wavelength of the emission spectrum at which the emission intensity is maximum is defined as the main peak wavelength. Note that in this specification, the main peak wavelength may be referred to as fluorescence main peak wavelength (FL-peak).
  • the fluorescent compound may be the dopant material or the host material.
  • the light-emitting layer is a single layer, only one of the dopant material and the host material may be the fluorescent compound, or both may be the fluorescent compound.
  • the light emitting layer includes a first light emitting layer (anode side) and a second light emitting layer (cathode side)
  • only one of the first light emitting layer and the second light emitting layer contains the fluorescent compound.
  • both of the light-emitting layers may contain the fluorescent compound.
  • the first light-emitting layer contains the fluorescent compound
  • only one of the dopant material and the host material contained in the first light-emitting layer may be the fluorescent compound, or both may be the fluorescent compound.
  • the second light emitting layer contains the fluorescent compound
  • only one of the dopant material and the host material contained in the second light emitting layer may be the fluorescent compound, or both may be the fluorescent compound. It may be a sexual compound.
  • Electron transport layer is a layer containing a material with high electron transport properties (electron transport material), and is formed between the light emitting layer and the cathode or, if present, between the electron injection layer and the light emitting layer. Ru.
  • the electron transport layer may have a single layer structure or a multilayer structure including two or more layers.
  • the electron transport layer may have a two-layer structure including a first electron transport layer (on the anode side) and a second electron transport layer (on the cathode side).
  • the electron transport layer of the single layer structure is preferably adjacent to the light emitting layer, and the electron transport layer of the multilayer structure that is closest to the anode, for example, the electron transport layer of the two layer structure is adjacent to the light emitting layer.
  • the electron transport layer of the two layer structure is adjacent to the light emitting layer.
  • one electron transport layer is adjacent to the light emitting layer.
  • the hole blocking described below is provided between the electron transport layer and the light emitting layer of the single layer structure, or between the electron transport layer and the light emitting layer closest to the light emitting layer in the multilayer structure. A layer or the like may be interposed.
  • the electron transport layer includes, for example, (1) Metal complexes such as aluminum complexes, beryllium complexes, zinc complexes, (2) Heteroaromatic compounds such as imidazole derivatives, benzimidazole derivatives, azine derivatives, carbazole derivatives, phenanthroline derivatives, (3) High molecular compounds can be used.
  • Metal complexes such as aluminum complexes, beryllium complexes, zinc complexes
  • Heteroaromatic compounds such as imidazole derivatives, benzimidazole derivatives, azine derivatives, carbazole derivatives, phenanthroline derivatives
  • High molecular compounds can be used.
  • metal complexes examples include tris(8-quinolinolato)aluminum(III) (abbreviation: Alq), tris(4-methyl-8-quinolinolato)aluminum (abbreviation: Almq3), bis(10-hydroxybenzo[h]quinolinato).
  • Beryllium (abbreviation: BeBq 2 ), bis(2-methyl-8-quinolinolato)(4-phenylphenolato)aluminum(III) (abbreviation: BAlq), bis(8-quinolinolato)zinc(II) (abbreviation: Znq) ), bis[2-(2-benzoxazolyl)phenolato]zinc(II) (abbreviation: ZnPBO), and bis[2-(2-benzothiazolyl)phenolato]zinc(II) (abbreviation: ZnBTZ).
  • BeBq 2 Beryllium (abbreviation: BeBq 2 ), bis(2-methyl-8-quinolinolato)(4-phenylphenolato)aluminum(III) (abbreviation: BAlq), bis(8-quinolinolato)zinc(II) (abbreviation: Znq) ), bis[2-(2-benzoxazolyl
  • polymer compounds include poly[(9,9-dihexylfluorene-2,7-diyl)-co-(pyridine-3,5-diyl)] (abbreviation: PF-Py), poly[(9, 9-dioctylfluorene-2,7-diyl)-co-(2,2'-bipyridine-6,6'-diyl)] (abbreviation: PF-BPy).
  • the above material has an electron mobility of 10 ⁇ 6 cm 2 /Vs or more. Note that materials other than those mentioned above may be used for the electron transport layer as long as they have higher electron transport properties than hole transport properties.
  • the electron injection layer is a layer containing a material with high electron injection properties.
  • the electron injection layer contains alkali metals such as lithium (Li) and cesium (Cs), alkaline earth metals such as magnesium (Mg), calcium (Ca), and strontium (Sr), europium (Eu), and ytterbium (Yb).
  • alkali metals such as lithium (Li) and cesium (Cs)
  • alkaline earth metals such as magnesium (Mg), calcium (Ca), and strontium (Sr), europium (Eu), and ytterbium (Yb).
  • Rare earth metals such as these and compounds containing these metals can be used. Examples of such compounds include alkali metal oxides, alkali metal halides, alkali metal-containing organic complexes, alkaline earth metal oxides, alkaline earth metal halides, alkaline earth metal-containing organic complexes, and rare earth metal oxides.
  • Examples include rare earth metal halides, and rare earth metal-containing organic complexes. Moreover, a plurality of these compounds can also be used in combination.
  • a material having an electron transport property containing an alkali metal, an alkaline earth metal, or a compound thereof, specifically a material containing magnesium (Mg) in Alq may be used. Note that in this case, electron injection from the cathode can be performed more efficiently.
  • a composite material made of a mixture of an organic compound and an electron donor may be used for the electron injection layer. Such a composite material has excellent electron injection and electron transport properties because the organic compound receives electrons from an electron donor.
  • the organic compound is preferably a material that is excellent in transporting received electrons, and specifically, for example, the above-mentioned materials constituting the electron transport layer (metal complexes, heteroaromatic compounds, etc.) are used. be able to.
  • the electron donor may be any material as long as it exhibits electron donating properties to organic compounds.
  • alkali metals, alkaline earth metals, and rare earth metals are preferred, and examples include lithium, cesium, magnesium, calcium, erbium, and ytterbium.
  • alkali metal oxides and alkaline earth metal oxides are preferable, and examples thereof include lithium oxide, calcium oxide, barium oxide, and the like.
  • Lewis bases such as magnesium oxide can also be used.
  • organic compounds such as tetrathiafulvalene (abbreviation: TTF) can also be used.
  • Cathode It is preferable to use a metal, an alloy, an electrically conductive compound, a mixture thereof, or the like having a small work function (specifically, 3.8 eV or less) for the cathode.
  • cathode materials include elements belonging to Group 1 or Group 2 of the periodic table of elements, that is, alkali metals such as lithium (Li) and cesium (Cs), and magnesium (Mg) and calcium (Ca). ), alkaline earth metals such as strontium (Sr), alloys containing these (for example, MgAg, AlLi), rare earth metals such as europium (Eu), ytterbium (Yb), and alloys containing these.
  • the cathode when forming a cathode using an alkali metal, an alkaline earth metal, or an alloy containing these, a vacuum evaporation method or a sputtering method can be used. Furthermore, when using silver paste or the like, a coating method, an inkjet method, etc. can be used. By providing an electron injection layer, the cathode can be formed using various conductive materials such as Al, Ag, ITO, graphene, silicon, or indium oxide-tin oxide containing silicon oxide, regardless of the size of the work function. can do. These conductive materials can be formed into films using a sputtering method, an inkjet method, a spin coating method, or the like.
  • an insulating layer made of an insulating thin film layer may be inserted between the pair of electrodes.
  • materials used for the insulating layer include aluminum oxide, lithium fluoride, lithium oxide, cesium fluoride, cesium oxide, magnesium oxide, magnesium fluoride, calcium oxide, calcium fluoride, aluminum nitride, titanium oxide, and silicon oxide. , germanium oxide, silicon nitride, boron nitride, molybdenum oxide, ruthenium oxide, vanadium oxide, and the like. Note that a mixture or a laminate of these may also be used.
  • the above-mentioned space layer is, for example, for the purpose of preventing excitons generated in the phosphorescent layer from diffusing into the fluorescent layer or adjusting carrier balance when a fluorescent layer and a phosphorescent layer are stacked.
  • This is a layer provided between a fluorescent layer and a phosphorescent layer.
  • a space layer can also be provided between a plurality of phosphorescence-emitting layers. Since the space layer is provided between the light-emitting layers, it is preferably made of a material that has both electron-transporting properties and hole-transporting properties. Further, in order to prevent triplet energy from diffusing in adjacent phosphorescent emitting layers, it is preferable that the triplet energy is 2.6 eV or more. Examples of the material used for the space layer include the same materials as those used for the hole transport layer described above.
  • a blocking layer such as an electron blocking layer, a hole blocking layer, an exciton blocking layer, etc. may be provided adjacent to the light emitting layer.
  • the electron blocking layer is a layer that prevents electrons from leaking from the light emitting layer to the hole transport layer
  • the hole blocking layer is a layer that prevents holes from leaking from the light emitting layer to the electron transport layer.
  • the exciton blocking layer has the function of preventing excitons generated in the light emitting layer from diffusing into surrounding layers and confining the excitons within the light emitting layer.
  • Each layer of the organic EL element can be formed by a conventionally known vapor deposition method, coating method, or the like.
  • vapor deposition methods such as vacuum evaporation method and molecular beam evaporation method (MBE method), or dipping method, spin coating method, casting method, bar coating method, roll coating method, etc. using a solution of a compound forming a layer. It can be formed by a known coating method.
  • the total thickness of the first hole transport layer and the second hole transport layer is preferably 30 nm or more and 150 nm or more.
  • the thickness is more preferably 40 nm or more and 130 nm or less.
  • the thickness of the second hole transport layer having a two-layer structure or a three-layer structure is preferably 5 nm or more, more preferably 20 nm or more, even more preferably 25 nm or more, and particularly preferably 35 nm or more. and preferably 100 nm or less.
  • the thickness of the hole transport layer adjacent to the light emitting layer is preferably 5 nm or more, more preferably 20 nm or more, even more preferably 25 nm or more, particularly preferably 30 nm or more, and Preferably it is 100 nm or less.
  • the ratio of the film thickness D2 of the second hole transport layer to the film thickness D1 of the first hole transport layer is preferably 0.3 ⁇ D2/D1 ⁇ 4.0, more preferably 0.5 ⁇ D2/D1 ⁇ 3.5, still more preferably 0.75 ⁇ D2/D1 ⁇ 3.0.
  • Preferred embodiments of the organic EL device of the present invention include, for example, (1) Organic EL device having a two-layered hole transport layer - A first embodiment in which the second hole transport layer contains the inventive compound and the first hole transport layer does not contain the inventive compound; - A second embodiment in which both the first hole transport layer and the second hole transport layer contain the inventive compound; - A third embodiment in which the first hole transport layer contains the invention compound and the second hole transport layer does not contain the invention compound; (2) an organic EL device having a three-layer hole transport layer; a fourth embodiment in which the first hole transport layer contains the inventive compound and the second and third hole transport layers do not contain the inventive compound; - A fifth embodiment in which the second hole transport layer contains the invention compound and the first and third hole transport layers do not contain the invention compound; - A sixth embodiment in which the third hole transport layer contains the invention compound and the first and second hole transport layers do not contain the invention compound; - A seventh embodiment in which the first and second hole transport layers contain the invention compound and the third hole transport layer does not contain the invention compound;
  • the organic EL element according to one embodiment of the present invention can be used in electronic devices such as display devices and light emitting devices.
  • display devices include display components such as organic EL panel modules, televisions, mobile phones, tablets, and personal computers.
  • the light emitting device include lighting, vehicle lamps, and the like.
  • the organic EL element can be used in display components such as organic EL panel modules, display devices such as televisions, mobile phones, and personal computers, and electronic devices such as lighting and light emitting devices of vehicle lamps.
  • Example 1 A glass substrate (manufactured by Geomatec Co., Ltd.) with a 25 mm x 75 mm x 1.1 mm ITO transparent electrode (anode) was ultrasonically cleaned in isopropyl alcohol for 5 minutes and then UV ozone cleaned for 30 minutes. The ITO film thickness was 130 nm. The glass substrate with the ITO transparent electrode after cleaning was mounted on a substrate holder of a vacuum evaporation apparatus, and first, compound HT-1 and compound HA were coated on the surface on which the transparent electrode was formed so as to cover the transparent electrode. A hole injection layer having a thickness of 10 nm was formed by vapor deposition.
  • the mass ratio of compound HT-1 and compound HA was 97:3.
  • compound HT-1 was deposited on the hole injection layer to form a first hole transport layer with a thickness of 40 nm.
  • compound Inv-1 was deposited on this first hole transport layer to form a second hole transport layer with a thickness of 40 nm.
  • compound HT-2 was deposited on the second hole transport layer to form a third hole transport layer with a thickness of 5 nm.
  • compound BH-1 (host material) and compound BD-1 (dopant material) were co-evaporated to form a first light-emitting layer with a thickness of 20 nm.
  • the mass ratio of compound BH-1 and compound BD-1 was 99:1.
  • compound ET-1 was deposited to form a first electron transport layer with a thickness of 5 nm.
  • compound ET-2 and Liq were co-evaporated to form a second electron transport layer with a thickness of 25 nm.
  • the mass ratio of compound ET-2 and Liq was 50:50.
  • Yb was deposited on the second electron transport layer to form an electron injection electrode with a thickness of 1 nm.
  • metal Al was deposited on this electron injection electrode to form a metal cathode having a thickness of 50 nm.
  • the layer structure of the organic EL device of Example 1 thus obtained is shown below.
  • the numbers in parentheses are film thicknesses (nm), and the ratios are mass ratios.
  • Example 2 and 3> Each organic EL device (I) was produced in the same manner as in Example 1, except that Compound Inv-4 was used in Example 2 and Compound Inv-5 was used in Example 3 instead of Compound Inv-1. did.
  • Example 4 A glass substrate (manufactured by Geomatec Co., Ltd.) with a 25 mm x 75 mm x 1.1 mm ITO transparent electrode (anode) was ultrasonically cleaned in isopropyl alcohol for 5 minutes and then UV ozone cleaned for 30 minutes. The ITO film thickness was 130 nm.
  • the glass substrate with the ITO transparent electrode after cleaning is mounted on a substrate holder of a vacuum evaporation apparatus, and first, compound Inv-1 and compound HA are coated on the surface on which the transparent electrode is formed so as to cover the transparent electrode.
  • a hole injection layer having a thickness of 10 nm was formed by vapor deposition.
  • the mass ratio of compound Inv-1 and compound HA was 97:3.
  • compound Inv-1 was deposited on the hole injection layer to form a first hole transport layer with a thickness of 80 nm.
  • compound HT-4 was deposited on the first hole transport layer to form a second hole transport layer with a thickness of 10 nm.
  • compound BH-2 (host material) and compound BD-2 (dopant material) were co-evaporated onto this second hole transport layer to form a light-emitting layer with a thickness of 25 nm.
  • the mass ratio of compound BH-2 and compound BD-2 was 96:4.
  • compound ET-3 was deposited to form a first electron transport layer with a thickness of 10 nm.
  • compound ET-4 was deposited to form a second electron transport layer having a thickness of 15 nm.
  • LiF was deposited to form an electron injection electrode with a thickness of 1 nm.
  • metal Al was deposited on this electron injection electrode to form a metal cathode having a thickness of 50 nm.
  • the layer structure of the organic EL element (II) of Example 4 thus obtained is shown below.
  • Example 4 except that Compound Inv-6 was used in Example 5, Compound Inv-7 was used in Example 6, and Compound Inv-8 was used in Example 7 instead of Compound Inv-1.
  • An organic EL device (II) was produced in the same manner.
  • Example 8 A glass substrate (manufactured by Geomatec Co., Ltd.) with a 25 mm x 75 mm x 1.1 mm ITO transparent electrode (anode) was ultrasonically cleaned in isopropyl alcohol for 5 minutes and then UV ozone cleaned for 30 minutes. The ITO film thickness was 130 nm. The glass substrate with the ITO transparent electrode after cleaning was mounted on a substrate holder of a vacuum evaporation apparatus, and first, compound HT-1 and compound HA were coated on the surface on which the transparent electrode was formed so as to cover the transparent electrode. A hole injection layer having a thickness of 10 nm was formed by vapor deposition.
  • the mass ratio of compound HT-1 and compound HA was 97:3.
  • compound HT-1 was deposited on the hole injection layer to form a first hole transport layer with a thickness of 40 nm.
  • compound Inv-2 was deposited on this first hole transport layer to form a second hole transport layer with a thickness of 45 nm.
  • compound HT-6 was deposited on the second hole transport layer to form a third hole transport layer with a thickness of 5 nm.
  • compound BH-1 (host material) and compound BD-3 (dopant material) were co-evaporated to form a first light-emitting layer with a thickness of 5 nm.
  • the mass ratio of compound BH-1 and compound BD-3 was 99:1.
  • compound BH-5 (host material) and compound BD-3 (dopant material) were co-evaporated onto this first light-emitting layer to form a second light-emitting layer with a thickness of 20 nm.
  • the mass ratio of compound BH-5 and compound BD-3 (BH-5:BD-3) was 99:1.
  • compound ET-1 was deposited to form a first electron transport layer having a thickness of 5 nm.
  • compound ET-2 and Liq were co-deposited to form a second electron transport layer having a thickness of 31 nm.
  • the mass ratio of compound ET-2 and Liq (ET-2:Liq) was 50:50.
  • Liq was evaporated to form an electron injection electrode with a thickness of 1 nm.
  • metal Al was deposited on this electron injection electrode to form a metal cathode with a thickness of 80 nm.
  • the layer structure of the organic EL device (III) of Example 8 thus obtained is shown below.
  • Example 9 An organic EL device (III) was produced in the same manner as in Example 8, except that compound Inv-3 was used instead of compound Inv-2.
  • Example 10 An organic EL device (III) was produced in the same manner as in Example 8, except that compound Inv-9 was used instead of compound Inv-2.
  • Example 11 An organic EL device (III) was produced in the same manner as in Example 8, except that compound BD-4 was used instead of compound BD-3.
  • Example 13 An organic EL device (III) was produced in the same manner as in Example 12, except that the mass ratio of compound BH-4 and compound BH-7 (BH-4:BH-7) was 50:50.
  • Example 14 An organic EL device (III) was produced in the same manner as in Example 12, except that the mass ratio of compound BH-4 and compound BH-7 (BH-4:BH-7) was 30:70.
  • Example 15 An organic EL device (III) was produced in the same manner as in Example 12, except that the mass ratio of compound BH-4 and compound BH-7 (BH-4:BH-7) was 20:80.
  • Example 16 A glass substrate (manufactured by Geomatec Co., Ltd.) with a 25 mm x 75 mm x 1.1 mm ITO transparent electrode (anode) was ultrasonically cleaned in isopropyl alcohol for 5 minutes and then UV ozone cleaned for 30 minutes. The ITO film thickness was 130 nm.
  • the glass substrate with the ITO transparent electrode after cleaning was mounted on a substrate holder of a vacuum evaporation apparatus, and first, compound HT-1 and compound HA were coated on the surface on which the transparent electrode was formed so as to cover the transparent electrode.
  • a hole injection layer having a thickness of 10 nm was formed by vapor deposition.
  • the mass ratio of compound HT-1 and compound HA was 97:3.
  • compound HT-1 was deposited on the hole injection layer to form a first hole transport layer with a thickness of 40 nm.
  • compound Inv-2 was deposited on this first hole transport layer to form a second hole transport layer with a thickness of 45 nm.
  • compound HT-2 was deposited on the second hole transport layer to form a third hole transport layer with a thickness of 5 nm.
  • compound BH-3 (host material) and compound BD-5 dopant material
  • the mass ratio of compound BH-3 and compound BD-5 was 99:1.
  • compound BH-6 (host material) and compound BD-5 (dopant material) were co-evaporated onto this first light-emitting layer to form a second light-emitting layer with a thickness of 20 nm.
  • the mass ratio of compound BH-6 and compound BD-5 was 99:1.
  • compound ET-3 was deposited to form a first electron transport layer with a thickness of 10 nm.
  • compound ET-4 was deposited to form a second electron transport layer having a thickness of 15 nm.
  • Example 17 An organic EL device (III) was produced in the same manner as in Example 8, except that compound HT-5 was used instead of compound HT-1, and compound Inv-1 was used instead of compound Inv-2.
  • the mass ratio of compound Inv-2 and compound HA was 97:3.
  • compound Inv-2 was deposited on the hole injection layer to form a first hole transport layer with a thickness of 85 nm.
  • compound HT-6 was deposited on the first hole transport layer to form a second hole transport layer with a thickness of 5 nm.
  • compound BH-1 host material
  • compound BD-3 dopant material
  • compound BH-5 (host material) and compound BD-3 (dopant material) were co-evaporated onto this first light-emitting layer to form a second light-emitting layer with a thickness of 15 nm.
  • the mass ratio of compound BH-5 and compound BD-3 (BH-5:BD-3) was 99:1.
  • compound ET-1 was deposited to form a first electron transport layer having a thickness of 5 nm.
  • compound ET-2 and Liq were co-deposited to form a second electron transport layer having a thickness of 31 nm.
  • the mass ratio of compound ET-2 and Liq (ET-2:Liq) was 50:50.
  • Example 18 except that Compound Inv-4 was used in Example 19, Compound Inv-3 was used in Example 20, and Compound Inv-9 was used in Example 21 instead of Compound Inv-2.
  • An organic EL device (IV) was produced in the same manner.
  • Example 22 An organic EL device (IV) was produced in the same manner as in Example 18, except that compound HT-7 was used instead of compound HT-6.
  • Example 23 An organic EL device (IV) was produced in the same manner as in Example 18, except that compound BH-9 was used instead of compound BH-5.
  • Example 24 The same procedure as in Example 18 was carried out, except that compound BH-3 was used instead of compound BH-1, compound BH-6 was used instead of compound BH-5, and compound BD-4 was used instead of compound BD-3.
  • An organic EL device (IV) was produced.
  • Example 25 A glass substrate (manufactured by Geomatec Co., Ltd.) with a 25 mm x 75 mm x 1.1 mm ITO transparent electrode (anode) was ultrasonically cleaned in isopropyl alcohol for 5 minutes and then UV ozone cleaned for 30 minutes. The ITO film thickness was 130 nm.
  • the glass substrate with the ITO transparent electrode after cleaning was mounted on a substrate holder of a vacuum evaporation apparatus, and first, compound Inv-2 and compound HA were coated on the surface on which the transparent electrode was formed so as to cover the transparent electrode.
  • a hole injection layer having a thickness of 10 nm was formed by vapor deposition.
  • compound BH-6 (host material) and compound BD-5 (dopant material) were co-evaporated onto this first light-emitting layer to form a second light-emitting layer with a thickness of 15 nm.
  • the mass ratio of compound BH-6 and compound BD-5 (BH-6:BD-5) was 99:1.
  • compound ET-3 was deposited to form a first electron transport layer with a thickness of 10 nm.
  • compound ET-4 was deposited to form a second electron transport layer having a thickness of 15 nm.
  • metal Al was deposited on this second electron transport layer to form a metal cathode having a thickness of 80 nm.
  • the layer structure of the organic EL element (IV) of Example 25 thus obtained is shown below.
  • the numbers in parentheses are film thicknesses (nm), and the ratios are mass ratios.
  • Example 26 An organic EL device (IV) was produced in the same manner as in Example 18, except that compound HT-9 was used instead of compound HT-6.
  • Example 27 An organic EL device (IV) was produced in the same manner as in Example 18, except that compound HT-10 was used instead of compound HT-6.
  • Example 28 In Example 18, compound BH-5 (host material) and compound BD-3 (dopant material) were co-deposited on the first light-emitting layer to form a second light-emitting layer with a thickness of 15 nm. -4 (host material), compound BH-7 (host material), and compound BD-3 (dopant material) were co-evaporated to form an organic EL layer with a thickness of 20 nm. A device (IV) was produced. The mass ratio of compound BH-4 and compound BH-7 (BH-4:BH-7) was 70:30, and the concentration of compound BD-3 was 1% by mass with respect to the entire second light emitting layer. .
  • Example 29 Same as in Example 28 except that compound HT-7 was used instead of compound HT-6 and the mass ratio of compound BH-4 and compound BH-7 (BH-4:BH-7) was 60:40. An organic EL device (IV) was produced.
  • Example 30 In Example 18, compound BH-5 (host material) and compound BD-3 (dopant material) were co-deposited on the first light-emitting layer to form a second light-emitting layer with a thickness of 15 nm. -8 (host material), compound BH-5 (host material), and compound BD-3 (dopant material) were co-evaporated to form an organic EL layer with a thickness of 20 nm. A device (IV) was produced. The mass ratio of compound BH-8 and compound BH-5 (BH-8:BH-5) was 70:30, and the concentration of compound BD-3 was 1% by mass with respect to the entire second light emitting layer. .
  • Examples 31 to 34 In place of compound HT-6, compound HT-11 was used in Example 31, compound HT-4 in Example 32, compound HT-12 in Example 33, and compound HT-13 in Example 34.
  • An organic EL device (IV) was produced in the same manner as in Example 18 except that .
  • organic EL device (IV) Regarding the obtained organic EL device (IV), the external quantum efficiency was determined to be 95% by the same method as organic EL device (I) and 95% by the same method as organic EL device (III). The lifespan was measured. The results are shown in Table 4.
  • the obtained residue was purified by silica gel column chromatography and recrystallization to obtain 3.29 g of white solid.
  • the yield was 40%.
  • the obtained solid was purified by silica gel column chromatography to obtain 1.88 g of white solid.
  • the yield was 26%.
  • the obtained solid was purified by silica gel column chromatography to obtain 1.88 g of white solid. The yield was 35%.

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Abstract

L'invention concerne un composé représenté par la formule (1). (les symboles dans la formule (1) sont tels que définis dans la description.) L'invention concerne également un élément électroluminescent organique qui contient le composé et un dispositif électronique qui comprend l'élément électroluminescent organique.
PCT/JP2023/018193 2022-05-18 2023-05-16 Composé, matériau d'élément électroluminescent organique, élément électroluminescent organique et dispositif électronique WO2023224020A1 (fr)

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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011003793A (ja) * 2009-06-19 2011-01-06 Idemitsu Kosan Co Ltd 有機ｅｌ素子
US20160301005A1 (en) * 2013-12-06 2016-10-13 Merck Patent Gmbh Compounds and organic electronic devices
US20170194569A1 (en) * 2015-12-23 2017-07-06 Samsung Display Co., Ltd Organic light-emitting device
KR20180066855A (ko) * 2016-12-09 2018-06-19 주식회사 엘지화학 신규한 아민계 화합물 및 이를 포함하는 유기 발광 소자
CN109096179A (zh) * 2018-07-23 2018-12-28 吉林奥来德光电材料股份有限公司 一种芳胺衍生物、其制备方法与应用
KR20190005522A (ko) * 2017-07-07 2019-01-16 에스에프씨 주식회사 저전압 구동이 가능하며, 고효율 및 장수명 특성을 가지는 유기 발광 소자
KR20190035567A (ko) * 2017-09-25 2019-04-03 머티어리얼사이언스 주식회사 유기 화합물 및 이를 포함하는 유기전계발광 소자
WO2019070082A1 (fr) * 2017-10-06 2019-04-11 出光興産株式会社 Composé, matériau pour élément électroluminescent organique, élément électroluminescent organique et dispositif électronique

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011003793A (ja) * 2009-06-19 2011-01-06 Idemitsu Kosan Co Ltd 有機ｅｌ素子
US20160301005A1 (en) * 2013-12-06 2016-10-13 Merck Patent Gmbh Compounds and organic electronic devices
US20170194569A1 (en) * 2015-12-23 2017-07-06 Samsung Display Co., Ltd Organic light-emitting device
KR20180066855A (ko) * 2016-12-09 2018-06-19 주식회사 엘지화학 신규한 아민계 화합물 및 이를 포함하는 유기 발광 소자
KR20190005522A (ko) * 2017-07-07 2019-01-16 에스에프씨 주식회사 저전압 구동이 가능하며, 고효율 및 장수명 특성을 가지는 유기 발광 소자
KR20190035567A (ko) * 2017-09-25 2019-04-03 머티어리얼사이언스 주식회사 유기 화합물 및 이를 포함하는 유기전계발광 소자
WO2019070082A1 (fr) * 2017-10-06 2019-04-11 出光興産株式会社 Composé, matériau pour élément électroluminescent organique, élément électroluminescent organique et dispositif électronique
CN109096179A (zh) * 2018-07-23 2018-12-28 吉林奥来德光电材料股份有限公司 一种芳胺衍生物、其制备方法与应用

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