WO2021251461A1 - 化合物、発光材料および発光素子 - Google Patents

化合物、発光材料および発光素子 Download PDF

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WO2021251461A1
WO2021251461A1 PCT/JP2021/022100 JP2021022100W WO2021251461A1 WO 2021251461 A1 WO2021251461 A1 WO 2021251461A1 JP 2021022100 W JP2021022100 W JP 2021022100W WO 2021251461 A1 WO2021251461 A1 WO 2021251461A1
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group
ring
light emitting
compound
substituted
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French (fr)
Japanese (ja)
Inventor
香織 藤澤
ヨン ジュ ジョ
善丈 鈴木
勇人 垣添
雄 稲田
ユソク ヤン
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Kyulux Inc
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Kyulux Inc
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Priority to JP2022530619A priority Critical patent/JP7709208B2/ja
Priority to CN202180041184.4A priority patent/CN115916785A/zh
Priority to KR1020227043919A priority patent/KR20230022872A/ko
Priority to US18/001,115 priority patent/US20230212177A1/en
Publication of WO2021251461A1 publication Critical patent/WO2021251461A1/ja
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04—Ortho-condensed systems
    • C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems
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    • C09K11/00—Luminescent materials, e.g. electroluminescent or chemiluminescent
    • C09K11/06—Luminescent materials, e.g. electroluminescent or chemiluminescent containing organic luminescent materials
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • 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
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
    • C09K2211/1033—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom with oxygen
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers

Definitions

  • the present invention relates to a compound useful as a light emitting material and a light emitting device using the compound.
  • organic electroluminescence elements organic electroluminescence elements
  • various measures have been taken to improve the luminous efficiency by newly developing and combining electron transport materials, hole transport materials, light emitting materials and the like constituting organic electroluminescence devices.
  • research on organic electroluminescence devices using delayed fluorescent materials can be seen.
  • the delayed fluorescent material is a material that emits fluorescence when returning from the excited singlet state to the ground state after an intersystem crossing from the excited triplet state to the excited singlet state occurs in the excited state. Fluorescence by such a pathway is called delayed fluorescence because it is observed later than the fluorescence from the excited singlet state directly generated from the ground state (normal fluorescence).
  • the probability of occurrence of the excited singlet state and the excited triplet state is statistically 25%: 75%, so that the excited singlet state directly generated is used. There is a limit to the improvement of light emission efficiency only by the fluorescence of.
  • the delayed fluorescent material not only the excited singlet state but also the excited triplet state can be used for fluorescence emission by the path via the above-mentioned inverse intersystem crossing, so that the emission is higher than that of the ordinary fluorescent material. Efficiency will be obtained.
  • 2CzPN having the following structure is a material that emits delayed fluorescence, it has a problem that the luminous efficiency is not high and the luminous efficiency is significantly reduced in a high current density region (see Non-Patent Document 1). ).
  • the present inventors have conducted repeated studies for the purpose of providing a more useful compound as a light emitting material for a light emitting device. Then, we proceeded with diligent studies for the purpose of deriving and generalizing the general formulas of compounds that are more useful as luminescent materials.
  • the present inventors have found that among benzonitrile derivatives, a compound having a structure satisfying a specific condition is useful as a light emitting material.
  • the present invention has been proposed based on these findings, and specifically has the following configurations.
  • R 1 to R 5 each independently have a substituted or unsubstituted aromatic hydrocarbon ring group or a substituted or unsubstituted aromatic heterocyclic group containing a nitrogen atom as a ring skeleton constituent atom.
  • R 1 ⁇ R 5 are each independently a donor group (provided that a substituted or unsubstituted aromatic hydrocarbon ring group, and a substituted or unsubstituted containing a nitrogen atom as a ring skeleton constituting atom (Excluding aromatic heterocyclic groups), all three donor groups are not identical, and at least one of the three donor groups is a benzofuran ring fused carbazolyl-9-. It is an ill group.
  • [2] The compound according to [1], wherein R 1 , R 2 and R 4 are independently donor groups.
  • R 1 , R 3 and R 4 are independent donor groups, respectively.
  • the compound of the present invention is useful as a light emitting material. Further, the compound of the present invention includes a compound that emits delayed fluorescence. The compound of the present invention is also useful as a material for an organic light emitting device.
  • the description of the constituent elements described below may be based on typical embodiments and specific examples of the present invention, but the present invention is not limited to such embodiments and specific examples.
  • the numerical range represented by using "-" in the present specification means a range including the numerical values before and after "-" as the lower limit value and the upper limit value.
  • the isotope species of hydrogen atoms existing in the molecule of the compound used in the present invention are not particularly limited, and for example, all the hydrogen atoms in the molecule may be 1 H, or some or all of them may be 2 H. (Duterium D) may be used.
  • R 1 to R 5 of the general formula (1) are independently substituted or unsubstituted aromatic hydrocarbon ring groups, or substituted or unsubstituted containing a nitrogen atom as a ring skeleton constituent atom. Represents an aromatic heterocyclic group.
  • aromatic hydrocarbon ring group means a group in which the ring (one ring) to be bonded is an aromatic hydrocarbon ring. For example, it contains a phenyl group bonded by one carbon atom constituting the ring skeleton of the benzene ring.
  • the hydrogen atoms constituting the bonded aromatic hydrocarbon ring may be substituted.
  • one or more rings may be condensed on the aromatic hydrocarbon ring to be bonded.
  • another ring may be condensed on the condensed ring. Examples of the ring to be condensed include an aromatic hydrocarbon ring, an aromatic heterocycle, an aliphatic hydrocarbon ring, and an aliphatic heterocycle.
  • Examples of the aromatic hydrocarbon ring include a benzene ring.
  • Examples of the aromatic heterocycle include a pyridine ring, a pyridazine ring, a pyrimidine ring, a pyrazine ring, a triazine ring, a pyrrole ring, a pyrazole ring, and an imidazole ring.
  • Examples of the aliphatic hydrocarbon ring include a cyclopentane ring, a cyclohexane ring, and a cycloheptane ring.
  • Examples of the aliphatic heterocycle include a piperidine ring, a pyrrolidine ring, and an imidazoline ring.
  • fused ring constituting the aromatic hydrocarbon ring examples include a naphthalene ring, an anthracene ring, a phenanthrene ring, a pyran ring, and a tetracene ring.
  • fused ring containing a hetero atom examples include an indole ring, an isoindole ring, a benzimidazole ring, a benzotriazole ring, a quinoline ring, an isoquinoline ring, a quinazoline ring, a quinoxaline ring, and a cinnoline ring.
  • fused rings they are bonded by carbon atoms constituting the benzene ring.
  • the number of carbon atoms of the substituted or unsubstituted aromatic hydrocarbon ring group that can be adopted by R 1 to R 5 is preferably 6 to 40, more preferably 6 to 30, and preferably 6 to 20. More preferred.
  • the number of ring skeleton constituent atoms of the ring to be bonded is preferably 6 to 14, more preferably 6 to 12, and even more preferably 6.
  • aromatic heterocyclic group as used in the present invention means that the ring (one ring) to be bonded is an aromatic heterocycle and is bonded by one carbon atom constituting the ring skeleton of the aromatic heterocycle. It includes, for example, a pyridyl group bonded at one carbon atom constituting the ring skeleton of a pyridine ring.
  • the aromatic heterocycles that can be taken by R 1 to R 5 include a nitrogen atom as a ring skeleton constituent atom of the ring (one ring) to be bonded.
  • the bonded ring may contain a heteroatom other than the nitrogen atom as a ring-skeleton-constituting atom, but it is preferable that the ring contains only a nitrogen atom as the ring-skeleton-constituting heteroatom.
  • the number of heteroatoms contained in the ring to be bonded is preferably 1 to 3, and more preferably 1 or 2.
  • Examples of the ring to be bonded include a pyridine ring, a pyridazine ring, a pyrimidine ring, a pyrazine ring, a triazine ring, a pyrrole ring, a pyrazole ring, and an imidazole ring.
  • the hydrogen atoms constituting the bonded ring may be substituted. Further, one or more rings may be condensed. Further, another ring may be condensed on the condensed ring.
  • the ring to be condensed include an aromatic hydrocarbon ring, an aromatic heterocycle, an aliphatic hydrocarbon ring, and an aliphatic heterocycle.
  • the aromatic hydrocarbon ring, the aromatic heterocycle, the aliphatic hydrocarbon ring and the aliphatic heterocycle referred to here refer to the corresponding description in the above description of the "aromatic hydrocarbon ring group". Can be done.
  • fused ring constituting the aromatic heterocycle examples include a quinoline ring, an isoquinoline ring, a quinazoline ring, a quinoxaline ring, a cinnoline ring, and a pteridine ring.
  • these fused rings they are bonded by carbon atoms constituting the ring skeleton of the heterocycle.
  • the number of carbon atoms of the substituted or unsubstituted aromatic heterocyclic group that can be adopted by R 1 to R 5 is preferably 3 to 30, more preferably 3 to 20, and further preferably 4 to 15. preferable.
  • the number of ring skeleton constituent atoms of the ring to be bonded is preferably 6 to 14, more preferably 6 to 12, and even more preferably 6.
  • the aromatic hydrocarbon ring group and the aromatic heterocyclic group that can be taken from R 1 to R 5 may be substituted.
  • substituents include an alkyl group, an alkenyl group, an aryl group, a heteroaryl group, an alkoxy group, an alkylthio group, an aryloxy group, an arylthio group, a heteroaryloxy group, a heteroarylthio group and a cyano group. These substituents may be substituted with yet another substituent.
  • Preferred groups of substituents include alkyl groups, aryl groups, alkoxy groups and alkylthio groups.
  • the "alkyl group" referred to here may be linear, branched or cyclic.
  • the number of carbon atoms of the alkyl group can be, for example, 1 or more, 2 or more, and 4 or more. Further, the number of carbon atoms can be 30 or less, 20 or less, 10 or less, 6 or less, and 4 or less. Specific examples of the alkyl group include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, n-pentyl group, isopentyl group, n-hexyl group and isohexyl group.
  • 2-Ethylhexyl group, n-heptyl group, isoheptyl group, n-octyl group, isooctyl group, n-nonyl group, isononyl group, n-decanyl group, isodecanyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group can be mentioned.
  • the alkyl group as a substituent may be further substituted with an aryl group.
  • the "alkenyl group" may be linear, branched or cyclic. Further, two or more of the linear portion, the annular portion and the branched portion may be mixed.
  • the carbon number of the alkenyl group can be, for example, 2 or more and 4 or more. Further, the number of carbon atoms can be 30 or less, 20 or less, 10 or less, 6 or less, and 4 or less.
  • Specific examples of the alkenyl group include ethenyl group, n-propenyl group, isopropenyl group, n-butenyl group, isobutenyl group, n-pentenyl group, isopentenyl group, n-hexenyl group, isohexenyl group and 2-ethylhexenyl group. Can be mentioned.
  • the alkenyl group as a substituent may be further substituted with a substituent.
  • the "aryl group” and the “heteroaryl group” may be a monocyclic ring or a condensed ring in which two or more rings are condensed.
  • the number of fused rings is preferably 2 to 6, and can be selected from, for example, 2 to 4.
  • the ring include a benzene ring, a pyridine ring, a pyrimidine ring, a triazine ring, a naphthalene ring, an anthracene ring, a phenanthrene ring, a triphenylene ring, a quinoline ring, a pyrazine ring, a quinoxaline ring, and a naphthylidine ring.
  • arylene group or the heteroarylene group examples include a phenyl group, a 1-naphthyl group, a 2-naphthyl group, a 1-anthrasenyl group, a 2-anthrasenyl group, a 9-anthrasenyl group, a 2-pyridyl group, a 3-pyridyl group, and 4 -Pyridyl groups can be mentioned.
  • the alkyl moiety of the "alkoxy group” and the "alkylthio group the above description and specific examples of the alkyl group can be referred to.
  • aryl portion of the "aryloxy group” and the “arylthio group” the above description and specific examples of the aryl group can be referred to.
  • heteroaryl portion of the “heteroaryloxy group” and the “heteroarylthio group” the above description and specific examples of the heteroaryl group can be referred to.
  • a substituted or unsubstituted aromatic hydrocarbon ring group or a substituted or unsubstituted aromatic heterocyclic group containing a nitrogen atom as a ring skeleton constituent atom can be any two. The two may be the same or different from each other, but are preferably the same. As a combination of the two, for example, a combination of R 3 and R 5 , R 2 and R 5 , R 1 and R 5 , and R 2 and R 4 can be mentioned as preferable examples. As a more preferable example, a combination of R 3 and R 5 , and R 2 and R 5 can be mentioned.
  • two of R 1 to R 5 of the general formula (1) are independently substituted or unsubstituted aromatic hydrocarbon ring groups. More preferably, R 3 and R 5 , R 2 and R 5 , R 1 and R 5 , or R 2 and R 4 , respectively, are independently substituted or unsubstituted aromatic hydrocarbon ring groups. For example, a group in which R 3 and R 5 are independently substituted or unsubstituted aromatic hydrocarbon ring groups, and a group in which R 2 and R 5 are independently substituted or unsubstituted aromatic hydrocarbon ring groups, respectively. Can be mentioned.
  • a substituted or unsubstituted aromatic hydrocarbon ring group which can be taken by two of R 1 to R 5 of the general formula (1) and a substituted or non-substituted aromatic hydrocarbon ring group containing a nitrogen atom as a ring skeleton constituent atom.
  • a specific example of the substituted aromatic heterocyclic group is shown.
  • R 1 to R 5 of the general formula (1) each independently represent a donor group.
  • the donor group referred to here is not a substituted or unsubstituted aromatic hydrocarbon ring group, nor is it a substituted or unsubstituted aromatic heterocyclic group containing a nitrogen atom as a ring skeleton constituent atom.
  • the "donor group” in the present invention is a group having a negative Hammet's ⁇ p value.
  • the “hammet ⁇ p value” is L. P. Proposed by Hammett, it quantifies the effect of substituents on the reaction rate or equilibrium of para-substituted benzene derivatives.
  • the donor group in the present invention is preferably a group containing a substituted amino group.
  • the substituent bonded to the nitrogen atom of the amino group is preferably a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group.
  • a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group is more preferable.
  • the substituted amino group is particularly preferably a substituted or unsubstituted diarylamino group or a substituted or unsubstituted diheteroarylamino group.
  • the donor group in the present invention may be a group bonded with a nitrogen atom of a substituted amino group or a group bonded with a group to which a substituted amino group is bonded.
  • the group to which the substituted amino group is bonded is preferably a ⁇ -conjugated group. More preferred are groups bonded at the nitrogen atom of the substituted amino group.
  • the alkyl group, alkenyl group, aryl group and heteroaryl group which are the substituents here the above-mentioned corresponding description regarding the substituent of the aromatic hydrocarbon ring group and the aromatic heterocyclic group can be referred to.
  • Particularly preferred as the donor group in the present invention is a substituted or unsubstituted carbazole-9-yl group.
  • the three donor groups present in the general formula (1) are independently substituted or unsubstituted carbazole-9-yl groups.
  • the substituent of the carbazole-9-yl group includes an alkyl group, an alkenyl group, an aryl group, a heteroaryl group, an alkoxy group, an alkylthio group, an aryloxy group, an arylthio group, a heteroaryloxy group, a heteroarylthio group and a substituted amino.
  • a group can be mentioned, and preferred substituents include an alkyl group, an aryl group, and a substituted amino group. For a description of the substituted amino group, the description in the previous paragraph can be referred to.
  • the substituted amino group referred to here includes a substituted or unsubstituted carbazolyl group, and particularly includes a substituted or unsubstituted carbazole-9-yl group.
  • the donor group in the present invention preferably has 5 or more atoms other than hydrogen atoms, preferably 10 or more, and more preferably 13 or more. Further, it is preferably 80 or less, more preferably 60 or less, and further preferably 40 or less.
  • At least one of the three donor groups present in the general formula (1) is a carbazolyl-9-yl group fused with a benzofuran ring.
  • the benzofuran ring may be a furan ring that is condensed to a carbazolyl-9-yl group, or a benzene ring that is condensed to a carbazolyl-9-yl group.
  • the former is preferable.
  • only one benzofuran ring may be condensed with the carbazolyl-9-yl group, or two or more benzofuran rings may be condensed with the carbazolyl-9-yl group. When two or more are condensed, their benzofuran rings may have the same structure or different structures.
  • the types of rings to be condensed may be the same or different.
  • the carbazolyl-9-yl group fused with the benzofuran ring may be substituted.
  • the substituents listed as the substituents of the carbazole-9-yl group can be preferably referred to. If the carbazolyl-9-yl group fused with the benzofuran ring has a ring fused to the carbazolyl-9-yl group as a ring other than the benzofuran ring, the fused ring is an aromatic hydrocarbon ring and a fat. It is preferable that only the ring is selected from the group consisting of group hydrocarbon rings, and more preferably only the aromatic hydrocarbon ring.
  • the carbazolyl-9-yl group fused with the benzofuran ring is also preferably one in which a ring other than the benzofuran ring is not condensed with the carbazolyl-9-yl group. Further, it is also preferable that the carbazolyl-9-yl group condensed with the benzofuran ring is unsubstituted.
  • the three donor groups existing in the general formula (1) are not all the same. All three may be different from each other, or two may be the same and one may be different. The latter is preferred. As a preferred embodiment of the present invention, there may be a case where two are carbazolyl-9-yl groups condensed with a benzofuran ring and the remaining one is a other donor group. Another preferred embodiment of the present invention may be the case where one is a carbazolyl-9-yl group condensed with a benzofuran ring and the other two are other donor groups. The other donor group is preferably a carbazolyl-9-yl group to which the benzofuran ring is not condensed.
  • the three donor groups may be any combination.
  • R 1 , R 2 and R 4 can be mentioned, and an embodiment in which R 1 and R 2 are the same but R 4 is different can be exemplified. It is also possible to exemplify an embodiment in which R 1 and R 4 are the same but R 2 is different. Further, it is possible to exemplify an embodiment in which R 2 and R 4 are the same but R 1 is different. As another preferable combination, R 1 , R 3 and R 4 can be mentioned, and an embodiment in which R 1 and R 3 are the same but R 4 is different can be exemplified.
  • R 1 and R 4 are the same but R 3 is different. Further, it is possible to exemplify an embodiment in which R 3 and R 4 are the same but R 1 is different.
  • R 2 and R 3 and R 4 can be mentioned, and an embodiment in which R 2 and R 3 are the same but R 4 is different can be exemplified. It is also possible to exemplify an embodiment in which R 2 and R 4 are the same but R 3 is different. Further, it is possible to exemplify an embodiment in which R 3 and R 4 are the same but R 2 is different.
  • R 1 , R 3 and R 5 can be mentioned, and an embodiment in which R 1 and R 3 are the same but R 5 is different can be exemplified. It is also possible to exemplify an embodiment in which R 1 and R 5 are the same but R 3 is different. Further, it is possible to exemplify an embodiment in which R 3 and R 5 are the same but R 1 is different.
  • D21 to D26 correspond to specific examples of the carbazolyl-9-yl group in which the benzofuran ring is condensed.
  • the compound represented by the general formula (1) is composed only of an atom selected from the group consisting of a carbon atom, a hydrogen atom, a nitrogen atom, an oxygen atom and a sulfur atom. In a preferred embodiment of the present invention, the compound represented by the general formula (1) is composed only of a carbon atom, a hydrogen atom, a nitrogen atom and an oxygen atom.
  • Tables 1 and 2 below specific examples of the compound represented by the general formula (1) are shown.
  • Table 1 and Table 2 the structure of the compound is shown by specifying R 1 to R 5 for each compound.
  • Table 2 a plurality of compounds are collectively displayed for each column. For example, if the compound 4537-4572 of Table 2, R 2 ⁇ R 5 are fixed to each D1, Ar1, D1, Ar1. Then, the compounds in which R 1 is D27 to D62 are designated as compounds 4537 to 4572 in order.
  • compounds 4573 to 5868 in the structure where R 1 is D1 and R 3 and R 5 are Ar 1, the compounds in which R 2 is D27 and R 4 is D27 to D62 are designated as compounds 4573 to 4608 in this order.
  • R 2 is D28 and R 4 is D27 to D62 as compounds 4609 to 4644 in order
  • R 3 is D29 and R 4 is D27 to D62 as compounds 4645 to 4680 in order.
  • the compound numbers are assigned in the same manner as in the above procedure, and finally, the compounds in which R 2 is D62 and R 4 is D27 to D62 are designated as compounds 5833 to 5868 in order.
  • Tables 1 and 2 the structures of compounds 1 to 16452 are individually specified and specifically disclosed herein. Further, compounds 1d to 16452d in which all hydrogen atoms existing in the molecules of compounds 1 to 16452 are replaced with deuterium atoms are disclosed.
  • Ar82 represents the same structure as Ar1d (a structure in which all hydrogen atoms of Ar1 are replaced with deuterium atoms).
  • the molecular weight of the compound represented by the general formula (1) is, for example, 1500 or less when the organic layer containing the compound represented by the general formula (1) is intended to be formed into a film by a vapor deposition method. It is preferably 1200 or less, more preferably 1000 or less, and even more preferably 900 or less. The lower limit of the molecular weight is the molecular weight of the smallest compound represented by the general formula (1).
  • the compound represented by the general formula (1) may be formed into a film by a coating method regardless of the molecular weight. By using the coating method, it is possible to form a film even if the compound has a relatively large molecular weight.
  • the compound represented by the general formula (1) has an advantage that it is easily dissolved in an organic solvent among the cyanobenzene compounds. Therefore, the compound represented by the general formula (1) is easy to apply the coating method and is easy to purify to increase the purity.
  • a compound containing a plurality of structures represented by the general formula (1) in the molecule as a light emitting material.
  • a polymer obtained by pre-existing a polymerizable group in the structure represented by the general formula (1) and polymerizing the polymerizable group as a light emitting material.
  • a monomer containing a polymerizable functional group is prepared in any of R 1 to R 5 of the general formula (1), and this is polymerized alone or copolymerized with another monomer.
  • a polymer having a repeating unit and use the polymer as a light emitting material.
  • dimers and trimers by coupling compounds having a structure represented by the general formula (1) to each other and use them as a light emitting material.
  • a polymer having a repeating unit containing a structure represented by the general formula (1) As an example of a polymer having a repeating unit containing a structure represented by the general formula (1), a polymer containing a structure represented by the following general formula (3) or (4) can be mentioned.
  • Q represents a group containing the structure represented by the general formula (1)
  • L 1 and L 2 represent a linking group.
  • the carbon number of the linking group is preferably 0 to 20, more preferably 1 to 15, and even more preferably 2 to 10.
  • X 11 represents an oxygen atom or a sulfur atom, and is preferably an oxygen atom.
  • L 11 represents a linking group, preferably a substituted or unsubstituted alkylene group, or a substituted or unsubstituted arylene group, and is a substituted or unsubstituted alkylene group having 1 to 10 carbon atoms, or a substituted or unsubstituted alkylene group. It is more preferably a phenylene group.
  • R 101 , R 102 , R 103 and R 104 each independently represent a substituent.
  • the linking group represented by L 1 and L 2 can be bonded to any of R 1 to R 5 of the general formula (1) constituting Q. Two or more linking groups may be linked to one Q to form a crosslinked structure or a network structure.
  • a hydroxy group is introduced into any of R 1 to R 5 of the general formula (1), and the following compound is used as a linker. It can be synthesized by reacting to introduce a polymerizable group and polymerizing the polymerizable group.
  • the polymer containing the structure represented by the general formula (1) in the molecule may be a polymer consisting only of repeating units having the structure represented by the general formula (1), or may have other structures. It may be a polymer containing a repeating unit having. Further, the repeating unit having the structure represented by the general formula (1) contained in the polymer may be a single type or two or more types. Examples of the repeating unit having no structure represented by the general formula (1) include those derived from a monomer used for ordinary copolymerization. For example, a repeating unit derived from a monomer having an ethylenically unsaturated bond such as ethylene and styrene can be mentioned.
  • the compound represented by the general formula (1) is a novel compound.
  • the compound represented by the general formula (1) can be synthesized by combining known reactions. For example, by using trifluorocyanobenzene as a starting material and reacting with a halide of an aromatic hydrocarbon in the presence of a catalyst, a derivative having two aromatic hydrocarbon ring groups introduced instead of a hydrogen atom can be obtained. can.
  • the target compound represented by the general formula (1) can be synthesized.
  • the synthesis example described later can be referred to.
  • other compounds represented by the general formula (1) can also be synthesized by using the same procedure or a known synthetic method.
  • the compound represented by the general formula (1) of the present invention is useful as a light emitting material for an organic light emitting device. Therefore, the compound represented by the general formula (1) of the present invention can be effectively used as a light emitting material in the light emitting layer of the organic light emitting device. Further, the compound represented by the general formula (1) of the present invention may be used as a host or an assist dopant.
  • the compound represented by the general formula (1) contains a delayed fluorescent substance that emits delayed fluorescence. That is, the present invention has an invention of a delayed fluorescent substance having a structure represented by the general formula (1), an invention using a compound represented by the general formula (1) as a delayed fluorescent substance, and the general formula (1).
  • An invention of a method of emitting delayed fluorescence using the represented compound is also provided.
  • An organic light emitting element using such a compound as a light emitting material has a feature that it emits delayed fluorescence and has high luminous efficiency. The principle will be explained below by taking an organic electroluminescence device as an example.
  • an organic electroluminescence element carriers are injected into a light emitting material from both positive and negative electrodes to generate an excited light emitting material and emit light.
  • 25% of the generated excitons are excited to the excited singlet state, and the remaining 75% are excited to the excited triplet state. Therefore, it is more efficient to use energy by using phosphorescence, which is light emitted from the excited triplet state.
  • phosphorescence which is light emitted from the excited triplet state.
  • the excited triplet state has a long lifetime, energy deactivation occurs due to saturation of the excited state and interaction with excitons in the excited triplet state, and the quantum yield of phosphorescence is generally not high in many cases.
  • the delayed fluorescent material radiates fluorescence by crossing the excited singlet state into the excited singlet state due to the triplet-triplet annihilation or absorption of heat energy after the energy transitions to the excited triplet state due to intersystem crossing or the like. do.
  • a heat-activated delayed fluorescent material that absorbs heat energy is considered to be particularly useful.
  • the excitons in the excited singlet state radiate fluorescence as usual.
  • excitons in the excited triplet state absorb the heat generated by the device, cross the terms to the excited singlet, and radiate fluorescence.
  • the light is emitted from the excited singlet, the light is emitted at the same wavelength as the fluorescence, but the life of the light (emission life) generated by the inverse intersystem crossing from the excited triplet state to the excited singlet state is normal. Since it is longer than the fluorescence of, it is observed as a fluorescence delayed from these. This can be defined as delayed fluorescence.
  • the ratio of compounds in the excited singlet state which normally produced only 25% by absorbing heat energy after carrier injection, is 25% or more. It will be possible to raise it to.
  • the heat of the device sufficiently causes intersystem crossing from the excited triplet state to the excited singlet state and emits delayed fluorescence. Efficiency can be dramatically improved.
  • an excellent organic light emitting element such as an organic photoluminescence element (organic PL element) or an organic electroluminescence element (organic EL element) is used.
  • the organic photoluminescence device has a structure in which at least a light emitting layer is formed on a substrate.
  • the organic electroluminescence device has at least an anode, a cathode, and a structure in which an organic layer is formed between the anode and the cathode.
  • the organic layer includes at least a light emitting layer, and may be composed of only a light emitting layer, or may have one or more organic layers in addition to the light emitting layer.
  • FIG. 1 shows a specific structural example of the organic electroluminescence device.
  • 1 is a substrate
  • 2 is an anode
  • 3 is a hole injection layer
  • 4 is a hole transport layer
  • 5 is a light emitting layer
  • 6 is an electron transport layer
  • 7 is a cathode.
  • each member and each layer of the organic electroluminescence device will be described.
  • the description of the substrate and the light emitting layer also applies to the substrate and the light emitting layer of the organic photoluminescence element.
  • the organic electroluminescence device of the present invention is preferably supported by a substrate.
  • the substrate is not particularly limited as long as it is conventionally used for organic electroluminescence devices, and for example, a substrate made of glass, transparent plastic, quartz, silicon, or the like can be used.
  • anode As the anode in the organic electroluminescence element, a metal having a large work function (4 eV or more), an alloy, an electrically conductive compound, or a mixture thereof as an electrode material is preferably used.
  • an electrode material include a metal such as Au, and a conductive transparent material such as CuI, indium tin oxide (ITO), SnO 2, and ZnO.
  • a material such as IDIXO (In 2 O 3- ZnO) that is amorphous and can produce a transparent conductive film may be used.
  • a thin film may be formed by forming a thin film of these electrode materials by a method such as thin film deposition or sputtering, and a pattern of a desired shape may be formed by a photolithography method, or when pattern accuracy is not required so much (about 100 ⁇ m or more). ), A pattern may be formed through a mask having a desired shape during vapor deposition or sputtering of the electrode material.
  • a coatable material such as an organic conductive compound
  • a wet film forming method such as a printing method or a coating method can also be used.
  • the sheet resistance as the anode is preferably several hundred ⁇ / sq. (Ohms per square) or less.
  • the film thickness depends on the material, but is usually selected in the range of 10 to 1000 nm, preferably 10 to 200 nm.
  • cathode a metal having a small work function (4 eV or less) (referred to as an electron-injectable metal), an alloy, an electrically conductive compound, or a mixture thereof is used as an electrode material.
  • electrode materials include sodium, sodium-potassium alloy, magnesium, lithium, magnesium / copper mixture, magnesium / silver mixture, magnesium / aluminum mixture, magnesium / indium mixture, aluminum / aluminum oxide (Al 2 O). 3 ) Examples include mixtures, indium, lithium / aluminum mixtures, rare earth metals and the like.
  • a mixture of an electron-injectable metal and a second metal which is a stable metal having a larger work function value than this for example, a magnesium / silver mixture, from the viewpoint of electron injectability and durability against oxidation and the like.
  • a magnesium / aluminum mixture, a magnesium / indium mixture, an aluminum / aluminum oxide (Al 2 O 3 ) mixture, a lithium / aluminum mixture, aluminum and the like are suitable.
  • the cathode can be produced by forming a thin film of these electrode materials by a method such as thin film deposition or sputtering.
  • the sheet resistance of the cathode is preferably several hundred ⁇ / sq.
  • the film thickness is usually selected in the range of 10 nm to 5 ⁇ m, preferably 50 to 200 nm.
  • the anode or the cathode of the organic electroluminescence element is transparent or translucent, because the emission brightness is improved.
  • a transparent or translucent cathode can be manufactured, and by applying this, an element having both the anode and the cathode transparent can be obtained. Can be made.
  • the light emitting layer is a layer that emits light after excitons are generated by recombination of holes and electrons injected from each of the anode and the cathode, and the light emitting material may be used alone for the light emitting layer. , Preferably include light emitting materials and host materials. As the light emitting material, one or more selected from the compound group of the present invention represented by the general formula (1) can be used. In order for the organic electroluminescence device and the organic photoluminescence device of the present invention to exhibit high light emission efficiency, it is important to confine the singlet excitons and triplet excitons generated in the light emitting material in the light emitting material.
  • a host material in addition to the light emitting material in the light emitting layer.
  • the host material an organic compound in which at least one of the excitation singlet energy and the excitation triplet energy has a higher value than that of the light emitting material of the present invention can be used.
  • the singlet excitons and triplet excitons generated in the light emitting material of the present invention can be confined in the molecules of the light emitting material of the present invention, and the luminous efficiency thereof can be sufficiently brought out.
  • any host material that can achieve high luminous efficiency is particularly restricted. Can be used in the present invention without.
  • the light emission is generated from the light emitting material of the present invention contained in the light emitting layer.
  • This emission includes both fluorescent and delayed fluorescence.
  • the light emitted from the host material may be partially or partially emitted.
  • the content of the compound represented by the general formula (1) in the light emitting layer is preferably less than 50% by weight.
  • the upper limit of the content of the compound represented by the general formula (1) is preferably less than 30% by weight, and the upper limit of the content is, for example, less than 20% by weight, less than 10% by weight, and 5% by weight. It can be less than%, less than 3% by weight, less than 1% by weight, and less than 0.5% by weight.
  • the lower limit is preferably 0.001% by weight or more, and may be, for example, more than 0.01% by weight, more than 0.1% by weight, more than 0.5% by weight, more than 1% by weight.
  • the host material in the light emitting layer is preferably an organic compound having a hole transporting ability and an electron transporting ability, preventing a long wavelength of light emission, and having a high glass transition temperature.
  • the compound represented by the general formula (1) can also be used as a host material for the light emitting layer.
  • the injection layer is a layer provided between the electrode and the organic layer in order to reduce the driving voltage and improve the emission brightness.
  • the injection layer includes a hole injection layer and an electron injection layer, and is located between the anode and the light emitting layer or the hole transport layer. And may be present between the cathode and the light emitting layer or the electron transport layer.
  • the injection layer can be provided as needed.
  • the blocking layer is a layer capable of blocking the diffusion of charges (electrons or holes) and / or excitons present in the light emitting layer to the outside of the light emitting layer.
  • the electron blocking layer can be placed between the light emitting layer and the hole transporting layer to prevent electrons from passing through the light emitting layer toward the hole transporting layer.
  • the hole blocking layer can be placed between the light emitting layer and the electron transporting layer to prevent holes from passing through the light emitting layer towards the electron transporting layer.
  • the blocking layer can also be used to prevent excitons from diffusing outside the light emitting layer. That is, the electron blocking layer and the hole blocking layer can also function as exciton blocking layers, respectively.
  • the electron blocking layer or exciton blocking layer is used to mean that one layer includes a layer having the functions of an electron blocking layer and an exciton blocking layer.
  • the hole blocking layer has a function of an electron transporting layer in a broad sense.
  • the hole blocking layer has a role of blocking the holes from reaching the electron transporting layer while transporting electrons, which can improve the recombination probability of electrons and holes in the light emitting layer.
  • the material of the hole blocking layer the material of the electron transport layer described later can be used as needed.
  • the electron blocking layer has a function of transporting holes in a broad sense.
  • the electron blocking layer has a role of blocking electrons from reaching the hole transporting layer while transporting holes, which can improve the probability of recombination of electrons and holes in the light emitting layer. ..
  • the exciton blocking layer is a layer for blocking excitons generated by recombination of holes and electrons in the light emitting layer from diffusing into the charge transport layer, and excitons are inserted by inserting this layer. It is possible to efficiently confine it in the light emitting layer, and it is possible to improve the light emitting efficiency of the element.
  • the exciton blocking layer can be inserted into either the anode side or the cathode side adjacent to the light emitting layer, and both can be inserted at the same time.
  • the layer when the exciton blocking layer is provided on the anode side, the layer can be inserted adjacent to the light emitting layer between the hole transport layer and the light emitting layer, and when inserted on the cathode side, the light emitting layer and the cathode are inserted.
  • the layer can be inserted adjacent to the light emitting layer between and.
  • a hole injection layer, an electron blocking layer, or the like can be provided between the anode and the exciton blocking layer adjacent to the anode side of the light emitting layer, and the cathode and the excitation adjacent to the cathode side of the light emitting layer can be provided.
  • An electron injection layer, an electron transport layer, a hole blocking layer, and the like can be provided between the child blocking layer and the electron blocking layer.
  • the blocking layer it is preferable that at least one of the excited singlet energy and the excited triplet energy of the material used as the blocking layer is higher than the excited singlet energy and the excited triplet energy of the light emitting material.
  • the hole transport layer is made of a hole transport material having a function of transporting holes, and the hole transport layer may be provided with a single layer or a plurality of layers.
  • the hole transporting material has either injection or transport of holes or an electron barrier property, and may be either an organic substance or an inorganic substance.
  • Known hole transporting materials that can be used include, for example, triazole derivatives, oxadiazole derivatives, imidazole derivatives, carbazole derivatives, indolocarbazole derivatives, polyarylalkane derivatives, pyrazoline derivatives and pyrazolone derivatives, phenylenediamine derivatives, arylamine derivatives, and the like.
  • Examples thereof include amino-substituted carcon derivatives, oxazole derivatives, styrylanthracene derivatives, fluorenone derivatives, hydrazone derivatives, stilben derivatives, silazane derivatives, aniline-based copolymers, and conductive polymer oligomers, especially thiophene oligomers, which include porphyrin compounds and aromatics. It is preferable to use a group tertiary amine compound and a styrylamine compound, and it is more preferable to use an aromatic tertiary amine compound.
  • the electron transport layer is made of a material having a function of transporting electrons, and the electron transport layer may be provided with a single layer or a plurality of layers.
  • the electron transporting material (which may also serve as a hole blocking material) may have a function of transmitting electrons injected from the cathode to the light emitting layer.
  • Examples of the electron transport layer that can be used include a nitro-substituted fluorene derivative, a diphenylquinone derivative, a thiopyrandioxide derivative, a carbodiimide, a freolenidene methane derivative, anthracinodimethane and anthrone derivatives, and an oxadiazole derivative.
  • a thiadiazole derivative in which the oxygen atom of the oxadiazole ring is replaced with a sulfur atom, and a quinoxaline derivative having a quinoxaline ring known as an electron-withdrawing group can also be used as an electron transport material.
  • a polymer material in which these materials are introduced into a polymer chain or these materials are used as a polymer main chain can also be used.
  • the compound represented by the general formula (1) may be used not only for one organic layer (for example, an electron transport layer) but also for a plurality of organic layers. ..
  • the compounds represented by the general formula (1) used for each organic layer may be the same or different from each other.
  • the above injection layer, blocking layer, hole blocking layer, electron blocking layer, exciton blocking layer, hole transport layer and the like are also represented by the general formula (1).
  • Compounds may be used.
  • the film forming method of these layers is not particularly limited, and may be formed by either a dry process or a wet process.
  • preferable compounds are given as materials that can be further added. For example, it may be added as a stabilizing material.
  • the organic electroluminescence device manufactured by the above method emits light by applying an electric field between the anode and the cathode of the obtained device. At this time, if the light is emitted by the excitation singlet energy, the light having a wavelength corresponding to the energy level is confirmed as fluorescent emission and delayed fluorescent emission. Further, in the case of light emission by excited triplet energy, the wavelength corresponding to the energy level is confirmed as phosphorescence. Since normal fluorescence has a shorter fluorescence lifetime than delayed fluorescence, the emission lifetime can be distinguished by fluorescence and delayed fluorescence.
  • the excitation triplet energy is unstable, the rate constant of heat deactivation is large, and the rate constant of light emission is small, so that the phosphorescence is immediately deactivated. Therefore, it can hardly be observed at room temperature.
  • the excited triplet energy of a normal organic compound it can be measured by observing light emission under extremely low temperature conditions.
  • the organic electroluminescence device of the present invention can be applied to any of a single device, a device having a structure arranged in an array, and a structure in which an anode and a cathode are arranged in an XY matrix. According to the present invention, by incorporating the compound represented by the general formula (1) in the light emitting layer, an organic light emitting device having greatly improved luminous efficiency can be obtained.
  • the organic light emitting device such as the organic electroluminescence device of the present invention can be further applied to various applications. For example, it is possible to manufacture an organic electroluminescence display device using the organic electroluminescence device of the present invention.
  • organic electroluminescence element of the present invention can be applied to organic electroluminescence lighting and a backlight, which are in great demand.
  • the emission characteristics are evaluated by a source meter (Caseley: 2400 series), a semiconductor parameter analyzer (Agilent Technology: E5273A), an optical power meter measuring device (Newport: 1930C), and an optical spectroscope. (Ocean Optics Co., Ltd .: USB2000), spectroradiometer (Topcon Co., Ltd .: SR-3) and streak camera (Hamamatsu Photonics Co., Ltd. C4334 type) were used.
  • Dimethylformamide (26 mL) was added to 1.04 g (6.24 mmol) of carbazole and 1.08 g (7.80 mmol) of potassium carbonate under a nitrogen stream, and the mixture was stirred at room temperature for 2 hours. 1.42 g (2.60 mmol) of Intermediate 2 was added to the reaction mixture, and the mixture was stirred at 100 ° C. for 16 hours. The reaction solution was returned to room temperature, water was added, and the precipitate was filtered off. The filtrate was washed with methanol and vacuum dried.
  • Examples 1 and 2 Fabrication and evaluation of thin film Compound 26 and PYD2Cz are different vapor deposition sources on a quartz substrate by a vacuum deposition method under the condition that the degree of vacuum is less than 1 ⁇ 10 -3 Pa.
  • a thin film having a concentration of compound 26 of 20% by weight was formed to a thickness of 100 nm to obtain a thin film of Example 1.
  • a thin film was formed according to the same procedure using compound 1626, comparative compound 1, and comparative compound 2 instead of compound 26, and these thin films were sequentially processed into thin films of Example 2, Comparative Example 1, and Comparative Example 2. And said.
  • the emission spectrum was observed using 300 nm excitation light, and the peak wavelength ( ⁇ max ) was read.
  • the lifetime of delayed fluorescence ( ⁇ d ) was obtained from the transient attenuation curve of emission observed using the same excitation light.
  • PLQY photoluminescence quantum efficiency
  • E ST is the lowest excited singlet energy (E S1) and the lowest excited triplet energy of the measurement target compound (E T1) found through the following procedure is a value obtained by calculating the E S1 -E T1 ..
  • Minimum excitation singlet energy (ES1 ) The fluorescence spectrum of the thin film of the compound to be measured was measured at room temperature (300K) (vertical axis: emission intensity, horizontal axis: wavelength). A tangent line was drawn for the rising edge of the emission spectrum on the short wave side, and the wavelength value ⁇ edge [nm] at the intersection of the tangent line and the horizontal axis was obtained. The value obtained by converting this wavelength value into an energy value by the following conversion formula was defined as ES1 .
  • E S1 [eV] 1239.85 / ⁇ edge (2) Minimum excited triplet energy ( ET1 )
  • the same thin film was cooled to 77 [K] with liquid nitrogen, the sample for phosphorescence measurement was irradiated with excitation light (300 nm), and phosphorescence was measured using a detector.
  • the emission spectrum after 100 milliseconds after the irradiation with the excitation light was defined as the phosphorescence spectrum.
  • a tangent line was drawn for the rising edge of the phosphorescence spectrum on the short wavelength side, and the wavelength value ⁇ edge [nm] at the intersection of the tangent line and the horizontal axis was obtained.
  • the value obtained by converting this wavelength value into an energy value using the above conversion formula was defined as ET1 .
  • the tangent to the rising edge of the phosphorescence spectrum on the short wavelength side was drawn as follows. When moving on the spectrum curve from the short wavelength side of the phosphorescence spectrum to the maximum value on the shortest wavelength side of the maximum values of the spectrum, tangents at each point on the curve were considered toward the long wavelength side. This tangent increases in slope as the curve rises (ie, as the vertical axis increases). The tangent line drawn at the point where the value of the slope reaches the maximum value was taken as the tangent line with respect to the rising edge of the phosphorescence spectrum on the short wavelength side.
  • the maximum point having a peak intensity of 10% or less of the maximum peak intensity of the spectrum is not included in the above-mentioned maximum value on the shortest wavelength side, and the value of the gradient closest to the maximum value on the shortest wavelength side is the maximum.
  • the tangent line drawn at the point where the value was taken was taken as the tangent line to the rising edge of the phosphorescent spectrum on the short wavelength side.
  • Examples 3 to 4 Preparation and evaluation of dope thin films having different host materials
  • the host materials of Examples 1 and 2 are changed from PYD2Cz to PPF, and the thin films of Examples 3 and 4 are formed according to the same procedure. did.
  • the lifetimes ( ⁇ d ) of the delayed fluorescence of Examples 3 and 4 were 12.5 ⁇ s and 18.8 ⁇ s, respectively.
  • the photoluminescence quantum efficiencies (PLQY) of Examples 3 and 4 were 70% and 81%, respectively.
  • Example 5 Fabrication and evaluation of thin films of similar light-emitting materials with different constituent elements
  • a compound 3387 is deposited on a quartz substrate by a vacuum vapor deposition method under conditions of a vacuum degree of less than 1 ⁇ 10 -3 Pa.
  • the neat thin film of Example 5 having a thickness of 100 nm was formed.
  • the neat thin film of Comparative Example 3 was formed by using Comparative Compound 3 instead of Compound 3387 according to the same procedure.
  • the peak wavelength ( ⁇ max ) was 493 nm in Example 5 and 499 nm in Comparative Example 3.
  • Example 5 using a compound having a carbazolyl-9-yl group condensed with a benzofuran ring is more than Comparative Example 3 using a compound having a carbazolyl-9-yl group condensed with a benzothiophene ring. It shows that the emission peak wavelength is on the short wavelength side and the emission efficiency is high. Further, a thin film having a concentration of 20% by weight of the compound 3387 is deposited on a quartz substrate by a vacuum vapor deposition method under the condition of a vacuum degree of less than 1 ⁇ 10 -3 Pa from different vapor deposition sources.
  • Comparative Example 3 It was formed to have a thickness of 100 nm and used as a dope thin film of Example 5. Further, the comparative compound 3 was used instead of the compound 3387 to form the dope thin film of Comparative Example 3 according to the same procedure. A transient attenuation curve of emission was obtained using 300 nm excitation light to determine the lifetime of delayed fluorescence ( ⁇ d ). As a result, Comparative Example 3 had 11.4 ⁇ s, while Example 5 had 7.4 ⁇ s, which was about 30% shorter.
  • Example 6 Fabrication and evaluation of organic electroluminescence device
  • ITO indium tin oxide
  • the layers were laminated at a degree of 1 ⁇ 10 -6 Pa.
  • a first hole injection layer made of a first hole injection material is formed on ITO
  • a second hole injection layer made of a second hole injection material is formed on the first hole injection layer
  • hole transport is formed on the second hole injection layer.
  • a hole transport layer made of a material was formed, and an electron blocking layer made of an electron blocking material was further formed on the hole transport layer.
  • compound 26 and the host material were co-deposited from different vapor deposition sources to form a light emitting layer having a concentration of compound 26 of 30% by weight.
  • a hole blocking layer made of a hole blocking material was formed, an electron transport layer was formed on the hole blocking layer, and an electrode was further formed on the electron transport layer.
  • the organic electroluminescence device of Example 6 was produced.
  • compound 1626 instead of compound 26 the organic electroluminescence device of Example 7 was produced by the same procedure.
  • Each of the organic electroluminescence devices of Examples 6 and 7 exhibits high luminous efficiency, a low drive voltage, and a high device life (device durability). Further, by using other compounds of the present invention, it is possible to provide an organic electroluminescence element which exhibits high luminous efficiency, has a low driving voltage, and has a long element life (element durability).

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WO2023140374A1 (ja) * 2022-01-24 2023-07-27 株式会社Kyulux 化合物、発光材料および発光素子
WO2024088239A1 (zh) * 2022-10-28 2024-05-02 清华大学 一种有机化合物及采用该化合物的有机电致发光器

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JP2023097788A (ja) * 2021-12-28 2023-07-10 株式会社Kyulux 化合物、発光材料および発光素子
JP7755298B2 (ja) 2021-12-28 2025-10-16 株式会社Kyulux 化合物、発光材料および発光素子
WO2023140374A1 (ja) * 2022-01-24 2023-07-27 株式会社Kyulux 化合物、発光材料および発光素子
WO2024088239A1 (zh) * 2022-10-28 2024-05-02 清华大学 一种有机化合物及采用该化合物的有机电致发光器

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