JP2012079915A - Light-emitting element material and light-emitting element - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an organic thin-film light-emitting element which achieves both high luminous efficiency and low driving voltage.SOLUTION: A light-emitting element material contains a specific pyrene compound represented by general formula (1).

Description

  The present invention relates to a pyrene compound useful as a fluorescent dye or a charge transport material, and a light emitting device using the same, and includes a display device, a flat panel display, a backlight, illumination, an interior, a sign, a signboard, an electrophotographic machine, and an optical signal The present invention relates to a light-emitting element that can be used in fields such as a generator.

  In recent years, research on organic thin-film light emitting devices that emit light when electrons injected from a cathode and holes injected from an anode are recombined in an organic phosphor sandwiched between both electrodes has been actively conducted. This light emitting element is characterized by thin light emission with high luminance under a low driving voltage and multicolor light emission by selecting a fluorescent material.

This study was conducted by C.D. W. Since Tang et al. Have shown that organic thin film devices emit light with high brightness, many research institutions have studied. The representative structure of the organic thin film light emitting device presented by the Kodak research group is a hole transporting diamine compound on the ITO glass substrate, 8-hydroxyquinoline aluminum as the light emitting layer, and Mg: Ag as the cathode in sequence. It was provided, and green light emission of 1,000 cd / m ² was possible with a driving voltage of about 10 V (see Non-Patent Document 1).

  In addition, organic thin-film light-emitting elements can be obtained in various emission colors by using various fluorescent materials for the light-emitting layer, and therefore, researches for practical application to displays and the like are actively conducted. Among the three primary color luminescent materials, research on the green luminescent material is the most advanced, and at present, intensive research is being conducted to improve the characteristics of the red and blue luminescent materials.

  The organic thin film light emitting element needs to satisfy the improvement in luminous efficiency, the reduction in driving voltage, and the improvement in durability. In particular, when the luminous efficiency is low, it is impossible to output an image that requires high luminance, and the amount of power consumption for outputting desired luminance increases. In order to improve the luminous efficiency, various luminescent materials have been developed (see, for example, Patent Documents 1 to 3). Moreover, the technique which dopes alkali metal to the material used as an electron carrying layer is disclosed (for example, refer patent documents 4-6).

International Publication WO2007 / 29798 Pamphlet International Publication WO2008 / 108256 Pamphlet JP2007-131723 (Claim 1) JP-A-2004-277377 (Claim 7) JP-A-2002-352961 (Claim 1) JP-A-2004-2297 (Claims 1, 15, 16)

“Applied Physics Letters”, (USA), 1987, 51, 12, p. 913-915

  However, in the methods as described in Patent Documents 1 to 3, in order to improve the light emission efficiency for all the light emission of RGB, it is necessary to improve each light emitting material. One method for improving the light emission efficiency more simply is to use the interference effect between the light emitted from the light emitting layer and the reflected light from the cathode, but the thin film layer is thickened under the optimum conditions. As a result, the drive voltage increases. Further, conventionally known combinations such as Patent Documents 4 to 6 are insufficient for achieving both low voltage driving and high luminous efficiency.

  SUMMARY OF THE INVENTION It is an object of the present invention to provide a light emitting device material that solves the problems of the prior art and enables an organic thin film light emitting device having both high luminous efficiency and low driving voltage, and a light emitting device using the same. It is.

  The present invention is a light emitting device material comprising a pyrene compound represented by the following general formula (1).

R ^{1 to} R ⁴ may be the same or different and are each hydrogen, alkyl group, cycloalkyl group, heterocyclic group, alkenyl group, cycloalkenyl group, alkynyl group, alkoxy group, alkylthio group, aryl ether group, aryl thioether Selected from the group consisting of a group, an aryl group, a heteroaryl group, a halogen, a carbonyl group, a carboxyl group, an oxycarbonyl group, a carbamoyl group, an amino group, a silyl group, and —P (═O) R ⁵ R ⁶ . R ⁵ and R ⁶ are an aryl group or a heteroaryl group, and adjacent substituents may form a ring. L is an arylene group. HAr is an aromatic heterocyclic group containing electron-accepting nitrogen. X ^{1 to} X ⁵ satisfy any of the following (A) to (D).
(A) X ² and X ³ and X ⁵ are hydrogen, and X ¹ and X ⁴ are aryl groups.
(B) X ¹ and X ³ and X ⁴ are hydrogen, and X ² and X ⁵ are aryl groups.
(C) X ¹ and X ⁴ and X ⁵ are hydrogen, and X ² and X ³ are aryl groups.
(D) X ¹ and X ² and X ⁴ are hydrogen, and X ³ and X ⁵ are aryl groups.
However, X ^{1 to} X ⁵ do not include an anthracene skeleton and a pyrene skeleton.

  According to the present invention, it is possible to provide an organic electroluminescence device having both high luminous efficiency and low driving voltage.

  The pyrene compound represented by the general formula (1) in the present invention will be described in detail.

R ^{1 to} R ⁴ may be the same or different and are each hydrogen, alkyl group, cycloalkyl group, heterocyclic group, alkenyl group, cycloalkenyl group, alkynyl group, alkoxy group, alkylthio group, aryl ether group, aryl thioether Selected from the group consisting of a group, an aryl group, a heteroaryl group, a halogen, a carbonyl group, a carboxyl group, an oxycarbonyl group, a carbamoyl group, an amino group, a silyl group, and —P (═O) R ⁵ R ⁶ . R ⁵ and R ⁶ are an aryl group or a heteroaryl group, and adjacent substituents may form a ring. L is an arylene group. HAr is an aromatic heterocyclic group containing electron-accepting nitrogen. X ^{1 to} X ⁵ satisfy any of the following (A) to (D).
(A) X ² and X ³ and X ⁵ are hydrogen, and X ¹ and X ⁴ are aryl groups.
(B) X ¹ and X ³ and X ⁴ are hydrogen, and X ² and X ⁵ are aryl groups.
(C) X ¹ and X ⁴ and X ⁵ are hydrogen, and X ² and X ³ are aryl groups.
(D) X ¹ and X ² and X ⁴ are hydrogen, and X ³ and X ⁵ are aryl groups.
However, X ^{1 to} X ⁵ do not include an anthracene skeleton and a pyrene skeleton.

  Of these substituents, hydrogen may be deuterium. The alkyl group represents, for example, a saturated aliphatic hydrocarbon group such as a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, a sec-butyl group, or a tert-butyl group. It may or may not have a substituent. There is no restriction | limiting in particular in the additional substituent in the case of being substituted, For example, an alkyl group, an aryl group, heteroaryl group etc. can be mentioned, This point is common also in the following description. The number of carbon atoms of the alkyl group is not particularly limited, but is usually in the range of 1 to 20 and more preferably 1 to 8 from the viewpoint of availability and cost.

  The cycloalkyl group represents, for example, a saturated alicyclic hydrocarbon group such as a cyclopropyl group, a cyclohexyl group, a norbornyl group, an adamantyl group, which may or may not have a substituent. Although carbon number of an alkyl group part is not specifically limited, Usually, it is the range of 3-20.

  The heterocyclic group refers to an aliphatic ring having atoms other than carbon, such as a pyran ring, a piperidine ring, and a cyclic amide, in the ring, which may or may not have a substituent. . Although carbon number of a heterocyclic group is not specifically limited, Usually, it is the range of 2-20.

  An alkenyl group shows the unsaturated aliphatic hydrocarbon group containing double bonds, such as a vinyl group, an allyl group, and a butadienyl group, and this may or may not have a substituent. Although carbon number of an alkenyl group is not specifically limited, Usually, it is the range of 2-20.

  The cycloalkenyl group refers to an unsaturated alicyclic hydrocarbon group containing a double bond such as a cyclopentenyl group, a cyclopentadienyl group, or a cyclohexenyl group, which may have a substituent. You don't have to.

  An alkynyl group shows the unsaturated aliphatic hydrocarbon group containing triple bonds, such as an ethynyl group, for example, and may or may not have a substituent. Although carbon number of an alkynyl group is not specifically limited, Usually, it is the range of 2-20.

  The alkoxy group refers to, for example, a functional group having an aliphatic hydrocarbon group bonded through an ether bond such as a methoxy group, an ethoxy group, or a propoxy group, and the aliphatic hydrocarbon group may have a substituent. It may not have. Although carbon number of an alkoxy group is not specifically limited, Usually, it is the range of 1-20.

  The alkylthio group is a group in which an oxygen atom of an ether bond of an alkoxy group is substituted with a sulfur atom. The hydrocarbon group of the alkylthio group may or may not have a substituent. Although carbon number of an alkylthio group is not specifically limited, Usually, it is the range of 1-20.

  An aryl ether group refers to a functional group to which an aromatic hydrocarbon group is bonded via an ether bond, such as a phenoxy group, and the aromatic hydrocarbon group may or may not have a substituent. Good. Although carbon number of an aryl ether group is not specifically limited, Usually, it is the range of 6-40.

  An aryl thioether group is one in which the oxygen atom of the ether bond of the aryl ether group is substituted with a sulfur atom. The aromatic hydrocarbon group in the aryl ether group may or may not have a substituent. Although carbon number of an aryl ether group is not specifically limited, Usually, it is the range of 6-40.

  An aryl group refers to an aromatic hydrocarbon group such as a phenyl group, a naphthyl group, a biphenyl group, a phenanthryl group, a terphenyl group, or a pyrenyl group. The aryl group may or may not have a substituent. Although carbon number of an aryl group is not specifically limited, Usually, it is the range of 6-40.

  A heteroaryl group is a furanyl group, thiophenyl group, pyridyl group, quinolinyl group, isoquinolinyl group, pyrazinyl group, pyrimidyl group, naphthyridyl group, benzofuranyl group, benzothiophenyl group, indolyl group, dibenzofuranyl group, dibenzothiophenyl group And a cyclic aromatic group having one or more atoms other than carbon in the ring, such as a carbazolyl group, which may be unsubstituted or substituted. Although carbon number of heteroaryl group is not specifically limited, Usually, it is the range of 2-30.

  The halogen atom represents fluorine, chlorine, bromine or iodine.

  The carbonyl group, carboxyl group, oxycarbonyl group, carbamoyl group, amino group, and phosphine oxide group may or may not have a substituent. Examples of the substituent include an alkyl group, a cycloalkyl group, and an aryl group. Group, heteroaryl group and the like, and these substituents may be further substituted.

  A silyl group refers to, for example, a functional group having a bond to a silicon atom, such as a trimethylsilyl group, which may or may not have a substituent. Although carbon number of a silyl group is not specifically limited, Usually, it is the range of 3-20. The number of silicon is usually in the range of 1 to 6.

  An arylene group refers to a divalent group derived from an aromatic hydrocarbon group such as a phenyl group, a naphthyl group, a biphenyl group, a phenanthryl group, or a terphenyl group, which has a substituent. It does not have to be. The carbon number of the arylene group is not particularly limited, but is usually in the range of 6 or more and 40 or less.

  An aromatic heterocyclic group containing electron-accepting nitrogen is a pyridyl group, a quinolinyl group, an isoquinolinyl group, a quinoxanyl group, a pyrazinyl group, a pyrimidyl group, a pyridazinyl group, a phenanthrolinyl group, an imidazopyridyl group, a triazyl group, an acridyl group Of the above heteroaryl groups, such as benzoimidazolyl, benzoxazolyl, and benzothiazolyl, a cyclic aromatic group having at least one electron-accepting nitrogen atom in the ring as an atom other than carbon. The aromatic heterocyclic group containing electron-accepting nitrogen may be unsubstituted or substituted. The number of electron-accepting nitrogen contained in the aromatic heterocyclic group containing electron-accepting nitrogen is not particularly limited, but is usually in the range of 1 or more and 3 or less. Moreover, there is no restriction | limiting in particular in the substituent in case the aromatic heterocyclic group containing electron-accepting nitrogen is substituted, For example, an alkyl group, an aryl group, heteroaryl group etc. can be mentioned.

  The electron-accepting nitrogen mentioned here represents a nitrogen atom forming a multiple bond with an adjacent atom. Since the nitrogen atom has a high electronegativity, the multiple bond has an electron accepting property. Therefore, an aromatic heterocycle containing electron-accepting nitrogen has a high electron affinity. The pyrene compound of the present invention having electron-accepting nitrogen makes it easy to receive electrons from a cathode having high electron affinity, and can be driven at a lower voltage. In addition, since the number of electrons supplied to the light emitting layer is increased and the recombination probability is increased, the light emission efficiency is improved. Although carbon number of the aromatic heterocyclic group containing electron-accepting nitrogen is not specifically limited, Usually, it is the range of 2-30. The connecting position of the aromatic heterocyclic group containing electron-accepting nitrogen may be any part. For example, in the case of a pyridyl group, it may be any of 2-pyridyl group, 3-pyridyl group and 4-pyridyl group.

  HAr is preferably a pyridyl group, a quinolinyl group, an isoquinolinyl group, a quinoxanyl group, a pyrimidyl group, a phenanthrolinyl group, a benzo [d] imidazolyl group, an imidazo [1,2-a] pyridyl group, or the like. More specifically, 2-pyridyl group, 3-pyridyl group, 4-pyridyl group, 2-quinolinyl group, 3-quinolinyl group, 6-quinolinyl group, 1-isoquinolinyl group, 3-isoquinolinyl group, 2-quinoxanyl group, 5-pyrimidyl group, 2-phenanthrolinyl group, 1-benzo [d] imidazolyl group, 2-benzo [d] imidazolyl group, 2-imidazol [1,2-a] pyridyl group, 3-imidazo [1, 2-a] pyridyl group and the like, more preferably 2-pyridyl group, 3-pyridyl group, 4-pyridyl group and the like.

  L is preferably a phenylene group, a naphthylene group or a biphenylene group. More specific examples include 1,4-phenylene group, 1,3-phenylene group, 1,2-phenylene group, 2,6-naphthylene group, 2,8-naphthylene group, 1,4-biphenylene group and the like. More preferably, a 1,3-phenylene group, a 1,4-phenylene group and the like can be mentioned.

The pyrene compound represented by the general formula (1) has an aromatic heterocycle containing a pyrene skeleton and electron-accepting nitrogen in the molecule. This makes it possible to achieve both high electron transportability and electrochemical stability of the pyrene skeleton and high electron acceptability of the aromatic heterocycle containing electron-accepting nitrogen, and exhibits high electron-injecting and transporting ability. Furthermore, it is preferable that two of X ^{1 to} X ⁵ are aryl groups, among which (A) X ² and X ³ and X ⁵ are hydrogen, and X ¹ and X ⁴ are aryl groups, ) X ¹ and X ³ and X ⁴ are hydrogen and X ² and X ⁵ are aryl groups, or (C) X ¹ and X ⁴ and X ⁵ are hydrogen, and X ² and X ³ are aryl groups Or (D) X ¹ and X ² and X ⁴ are hydrogen, and X ³ and X ⁵ are aryl groups, whereby strong fluorescence intensity is maintained in a solid or thin film state, and high-efficiency light emission is achieved. It becomes possible.

  Preferable examples when each X is an aryl group include a phenyl group, a naphthyl group, and a biphenyl group. In addition, these groups may be substituted with an aryl group and / or an alkyl group consisting only of hydrocarbons.

  Since aromatic heterocycles containing electron-accepting nitrogen are vulnerable to oxidation, bonding via L is more electrochemically stable than bonding directly to the pyrene skeleton. This creates a synergistic effect with the high electron transport property of the pyrene skeleton, and expresses higher electron injecting and transporting ability.

  A known method can be used for the synthesis of the pyrene compound represented by the general formula (1). Methods for introducing an aryl group or heteroaryl group into the pyrene skeleton include, for example, a method using a coupling reaction under a palladium or nickel catalyst with a halogenated pyrene derivative and an aryl or heteroaryl metal reagent, or aryl halide or halogenation. Examples include, but are not limited to, a method using a coupling reaction of teloaryl and a pyrene derivative boronic acid under a palladium or nickel catalyst. As a method for introducing an aryl group or heteroaryl group into the 7-position of the pyrene skeleton, for example, after introducing a boronic acid ester into the 2-position of pyrene under an iridium catalyst, a pyrene boronic acid ester under a palladium or nickel catalyst is used. And a method using a coupling reaction of a halogenated aryl or a halogenated heteroaryl, but is not limited thereto.

  Although it does not specifically limit as a pyrene compound represented by the said General formula (1), Specifically, the following examples are given. In addition, as a combination of each X, it is not restricted to what was illustrated, The compound which shows the same characteristic can be obtained by combining the structure shown by these suitably.

By using the pyrene compound represented by the general formula (1) in the present invention for any layer of the light-emitting element, a high light-emitting efficiency and a light-emitting element with a low driving voltage can be obtained. In addition,
The pyrene compound represented by the general formula (1) in the present invention can also be used as a protective film when light is extracted from the light emitting element.

  Since the pyrene compound represented by the general formula (1) has high electron injection and transport ability, light emission efficiency, and thin film stability, it is preferably used for the light emitting layer or the electron transport layer of the light emitting element. In particular, since it has an excellent electron injecting and transporting capability, it is preferably used for the electron transporting layer.

  Next, embodiments of the light emitting device of the present invention will be described in detail. The light-emitting element of the present invention has an anode and a cathode, and an organic layer interposed between the anode and the cathode. The organic layer includes at least a light-emitting layer, and the light-emitting layer emits light by electric energy.

  The organic layer is composed of only the light emitting layer, 1) a hole transport layer / light emitting layer / electron transport layer, 2) a light emitting layer / electron transport layer, and 3) a hole transport layer / light emitting layer, etc. A configuration is mentioned. Each of the layers may be a single layer or a plurality of layers. When the hole transport layer and the electron transport layer have a plurality of layers, the layers in contact with the electrodes may be referred to as a hole injection layer and an electron injection layer, respectively. The material is included in the hole transport material, and the electron injection material is included in the electron transport material.

  In the light emitting device of the present invention, the anode and the cathode have a role for supplying a sufficient current for light emission of the device, and at least one of them is preferably transparent or translucent in order to extract light. Usually, the anode formed on the substrate is a transparent electrode.

  The material used for the anode is a material that can efficiently inject holes into the organic layer, and is transparent or translucent to extract light. Tin oxide, indium oxide, indium tin oxide (ITO) indium zinc oxide (IZO) Although not particularly limited, such as conductive metal oxides such as, metals such as gold, silver and chromium, inorganic conductive materials such as copper iodide and copper sulfide, conductive polymers such as polythiophene, polypyrrole and polyaniline It is particularly desirable to use ITO glass or Nesa glass. These electrode materials may be used alone, or a plurality of materials may be laminated or mixed. The resistance of the transparent electrode is not limited as long as a current sufficient for light emission of the element can be supplied, but it is desirable that the resistance be low from the viewpoint of power consumption of the element. For example, an ITO substrate with a resistance of 300Ω / □ or less will function as a device electrode, but since it is now possible to supply a substrate with a resistance of approximately 10Ω / □, use a substrate with a low resistance of 20Ω / □ or less. Is particularly desirable. The thickness of ITO can be arbitrarily selected according to the resistance value, but is usually used in a range of 100 to 300 nm.

In order to maintain the mechanical strength of the light emitting element, the light emitting element is preferably formed over a substrate. As the substrate, a glass substrate such as soda glass or non-alkali glass is preferably used. As the thickness of the glass substrate, it is sufficient that the thickness is sufficient to maintain the mechanical strength. As for the glass material, alkali-free glass is preferred because it is better that there are fewer ions eluted from the glass. Alternatively, soda lime glass provided with a barrier coat such as SiO ₂ is also commercially available and can be used. Furthermore, if the first electrode functions stably, the substrate need not be glass, and for example, an anode may be formed on a plastic substrate. The ITO film forming method is not particularly limited, such as an electron beam method, a sputtering method, and a chemical reaction method.

  The material used for the cathode is not particularly limited as long as it can efficiently inject electrons into the light emitting layer. Generally, metals such as platinum, gold, silver, copper, iron, tin, aluminum, and indium, or alloys and multilayer stacks of these metals with low work function metals such as lithium, sodium, potassium, calcium, and magnesium Is preferred. Among these, aluminum, silver, and magnesium are preferable as the main component from the viewpoints of electrical resistance, ease of film formation, film stability, luminous efficiency, and the like. In particular, magnesium and silver are preferable because electron injection into the electron transport layer and the electron injection layer in the present invention is facilitated and low voltage driving is possible.

  Furthermore, for cathode protection, metals such as platinum, gold, silver, copper, iron, tin, aluminum and indium, or alloys using these metals, inorganic materials such as silica, titania and silicon nitride, polyvinyl alcohol, polyvinyl chloride As a preferred example, an organic polymer compound such as a hydrocarbon polymer compound is laminated on the cathode as a protective film layer. However, in the case of an element structure (top emission structure) that extracts light from the cathode side, the protective film layer is selected from materials that are light transmissive in the visible light region. The production method of these electrodes is not particularly limited, such as resistance heating, electron beam, sputtering, ion plating and coating.

  The hole transport layer is formed by a method of laminating or mixing one or more hole transport materials or a method using a mixture of a hole transport material and a polymer binder. Alternatively, the hole transport layer may be formed by adding an inorganic salt such as iron (III) chloride to the hole transport material. The hole transport material needs to efficiently transport holes from the positive electrode between electrodes to which an electric field is applied, and has a high hole injection efficiency, and it is desirable to transport the injected holes efficiently. For this purpose, it is required that the material has an appropriate ionization potential, has a high hole mobility, is excellent in stability, and does not easily generate trapping impurities during manufacture and use. Although it does not specifically limit as a substance which satisfy | fills such conditions, 4,4'-bis (N- (3-methylphenyl) -N-phenylamino) biphenyl, 4,4'-bis (N-- Triphenylamine derivatives such as (1-naphthyl) -N-phenylamino) biphenyl, 4,4 ′, 4 ″ -tris (3-methylphenyl (phenyl) amino) triphenylamine, bis (N-allylcarbazole) or Biscarbazole derivatives such as bis (N-alkylcarbazole), pyrazoline derivatives, stilbene compounds, hydrazone compounds, benzofuran derivatives and thiophene derivatives, oxadiazole derivatives, phthalocyanine derivatives, porphyrin derivatives and other heterocyclic compounds, fullerene derivatives, polymers In the system, the polycarbonate having the monomer in the side chain Chromatography with or styrene derivatives, polythiophene, polyaniline, polyfluorene, polyvinylcarbazole and polysilane are preferred.

  Furthermore, inorganic compounds such as p-type Si and p-type SiC can also be used. Further, a compound represented by the following general formula (3), tetrafluorotetracyanoquinodimethane (4F-TCNQ), or molybdenum oxide can also be used.

R ^{7 to} R ¹² may be the same or different and are selected from the group consisting of halogen, sulfonyl group, carbonyl group, nitro group, cyano group, and trifluoromethyl group.

  Among these, the compound (4) (1,4,5,8,9,12-hexaazatriphenylenehexacarbonitrile) is preferably contained in the hole transporting layer or the hole injecting layer because it can be driven at a lower voltage.

  In the present invention, the light emitting layer may be either a single layer or a plurality of layers, each formed of a light emitting material (host material, dopant material), which may be a mixture of a host material and a dopant material or a host material alone. It may be either. That is, in the light emitting element of the present invention, only the host material or the dopant material may emit light in each light emitting layer, or both the host material and the dopant material may emit light. From the viewpoint of efficiently using electric energy and obtaining light emission with high color purity, the light emitting layer is preferably composed of a mixture of a host material and a dopant material. Further, the host material and the dopant material may be either one kind or a plurality of combinations, respectively. The dopant material may be included in the entire host material or may be partially included. The dopant material may be laminated or dispersed. The dopant material can control the emission color. If the amount of the dopant material is too large, a concentration quenching phenomenon occurs, so that it is preferably used at 20% by weight or less, more preferably 10% by weight or less with respect to the host material. The doping method can be formed by a co-evaporation method with a host material, but may be simultaneously deposited after being previously mixed with the host material.

  The pyrene compound represented by the general formula (1) is suitably used as a light emitting material because it has high light emission performance. Moreover, since the pyrene compound represented by General formula (1) shows strong light emission in the ultraviolet to blue region (300 to 450 nm region), it can be suitably used as a blue light emitting material. When used as a host-dopant light emitting material, the pyrene compound of the present invention may be used as a dopant material, but is preferably used as a host material because of its excellent thin film stability.

  In addition to the pyrene compound represented by the general formula (1), the luminescent material specifically includes a condensed ring derivative such as anthracene or pyrene, which has been known as a luminescent material, tris (8-quinolinolato) aluminum. Starting metal chelated oxinoid compounds, bisstyryl derivatives such as bisstyryl anthracene derivatives and distyrylbenzene derivatives, tetraphenylbutadiene derivatives, indene derivatives, coumarin derivatives, oxadiazole derivatives, pyrrolopyridine derivatives, perinone derivatives, cyclopentadiene derivatives, Oxadiazole derivatives, thiadiazolopyridine derivatives, dibenzofuran derivatives, carbazole derivatives, indolocarbazole derivatives, in the polymer system, polyphenylene vinylene derivatives, polyparaphenylene derivatives, Such Fen derivative is not particularly limited but can be used.

  The host material contained in the light emitting material need not be limited to only one pyrene compound represented by the general formula (1), and a plurality of pyrene compounds of the present invention may be used in combination, or one of the other host materials. The above may be used as a mixture with the pyrene compound of the present invention. Although it does not specifically limit as a host material which can be mixed, The compound which has condensed aryl rings, such as naphthalene, anthracene, phenanthrene, pyrene, chrysene, naphthacene, triphenylene, perylene, fluoranthene, fluorene, indene, its derivative, N, N ' Metal chelated oxinoid compounds including aromatic amine derivatives such as dinaphthyl-N, N′-diphenyl-4,4′-diphenyl-1,1′-diamine, tris (8-quinolinato) aluminum (III), Bisstyryl derivatives such as distyrylbenzene derivatives, tetraphenylbutadiene derivatives, indene derivatives, coumarin derivatives, oxadiazole derivatives, pyrrolopyridine derivatives, perinone derivatives, cyclopentadiene derivatives, pyrrolopyrrole derivatives, thiadia In the case of lopyridine derivatives, dibenzofuran derivatives, carbazole derivatives, indolocarbazole derivatives, triazine derivatives, and polymer systems, polyphenylene vinylene derivatives, polyparaphenylene derivatives, polyfluorene derivatives, polyvinyl carbazole derivatives, polythiophene derivatives, etc. can be used but are particularly limited is not. Among them, as a host used when the light emitting layer emits phosphorescence, a metal chelated oxinoid compound, a dibenzofuran derivative, a carbazole derivative, an indolocarbazole derivative, a triazine derivative, or the like is preferably used.

  The dopant material is not particularly limited, but a compound having a condensed aryl ring such as naphthalene, anthracene, phenanthrene, pyrene, chrysene, triphenylene, perylene, fluoranthene, fluorene, indene or a derivative thereof (for example, 2- (benzothiazol-2-yl) ) -9,10-diphenylanthracene or 5,6,11,12-tetraphenylnaphthacene), furan, pyrrole, thiophene, silole, 9-silafluorene, 9,9'-spirobisilafluorene, benzothiophene, Compounds having heteroaryl rings such as benzofuran, indole, dibenzothiophene, dibenzofuran, imidazopyridine, phenanthroline, pyridine, pyrazine, naphthyridine, quinoxaline, pyrrolopyridine, thioxanthene and the like Conductor, borane derivative, distyrylbenzene derivative, 4,4′-bis (2- (4-diphenylaminophenyl) ethenyl) biphenyl, 4,4′-bis (N- (stilben-4-yl) -N-phenyl Aminostyryl derivatives such as amino) stilbene, aromatic acetylene derivatives, tetraphenylbutadiene derivatives, stilbene derivatives, aldazine derivatives, pyromethene derivatives, diketopyrrolo [3,4-c] pyrrole derivatives, 2,3,5,6-1H, 4H -Coumarin derivatives such as tetrahydro-9- (2'-benzothiazolyl) quinolidino [9,9a, 1-gh] coumarin, azole derivatives such as imidazole, thiazole, thiadiazole, carbazole, oxazole, oxadiazole, triazole and metal complexes thereof And N, N′− Phenyl -N, etc. N'- di (3-methylphenyl) -4,4'-aromatic amine derivative typified by diphenyl 1,1'-diamine.

  In addition, the dopant used when the light emitting layer emits phosphorescence includes iridium (Ir), ruthenium (Ru), palladium (Pd), platinum (Pt), osmium (Os), and rhenium (Re). A metal complex compound containing at least one metal selected from the group is preferable. The ligand preferably has a nitrogen-containing aromatic heterocycle such as a phenylpyridine skeleton or a phenylquinoline skeleton. However, it is not limited to these, and an appropriate complex is selected from the relationship with the required emission color, device performance, and host compound.

  In the present invention, the electron transport layer is a layer in which electrons are injected from the cathode and further transports electrons. The electron transport layer has high electron injection efficiency, and it is desired to efficiently transport injected electrons. For this reason, the electron transport layer is required to be a substance having a high electron affinity, a high electron mobility, excellent stability, and a trapping impurity that is unlikely to be generated during manufacture and use. In particular, in the case of stacking a thick film, a compound having a molecular weight of 400 or more that maintains a stable film quality is preferable because a low molecular weight compound is likely to be crystallized to deteriorate the film quality. However, considering the transport balance between holes and electrons, if the electron transport layer mainly plays a role of effectively preventing the holes from the anode from recombining and flowing to the cathode side, the electron transport Even if it is made of a material that does not have a high capability, the effect of improving the luminous efficiency is equivalent to that of a material that has a high electron transport capability. Therefore, the electron transport layer in the present invention includes a hole blocking layer that can efficiently block the movement of holes as the same meaning.

  The pyrene compound represented by the general formula (1) is a compound that satisfies the above conditions and has a high electron injecting and transporting capability, so that it is also suitably used as an electron transporting material.

  When the electron transport layer further contains a donor compound, the compatibility with the donor compound in a thin film state is improved, and higher electron injection / transport ability is exhibited. By the action of the mixture layer, the transport of electrons from the cathode to the light emitting layer is promoted, and both high luminous efficiency and low driving voltage can be achieved.

  The electron transport material used in the present invention need not be limited to each one of the pyrene compounds represented by the general formula (1), and a plurality of pyrene compounds may be used in combination, or one or more other electron transport materials may be used. May be used as long as the effects of the present invention are not impaired. The electron transport material that can be mixed is not particularly limited, but is a compound having a condensed aryl ring such as naphthalene, anthracene, or pyrene or a derivative thereof, or a styryl-based fragrance typified by 4,4′-bis (diphenylethenyl) biphenyl. Ring derivatives, perylene derivatives, perinone derivatives, coumarin derivatives, naphthalimide derivatives, quinone derivatives such as anthraquinone and diphenoquinone, phosphorus oxide derivatives, carbazole derivatives and indole derivatives, quinolinol complexes such as tris (8-quinolinolato) aluminum (III) and hydroxy Examples include hydroxyazole complexes such as phenyloxazole complexes, azomethine complexes, tropolone metal complexes, and flavonol metal complexes.

  Next, the donor compound will be described. The donor compound in the present invention is a compound that facilitates electron injection from the cathode or the electron injection layer to the electron transport layer by improving the electron injection barrier, and further improves the electrical conductivity of the electron transport layer. That is, in the light-emitting device of the present invention, the electron transport layer is more preferably doped with a donor compound in order to improve the electron transport capability in addition to the pyrene compound represented by the general formula (1).

  Preferred examples of the donor compound in the present invention include an alkali metal, an inorganic salt containing an alkali metal, a complex of an alkali metal and an organic substance, an alkaline earth metal, an inorganic salt containing an alkaline earth metal, or an alkaline earth metal. And a complex of organic substance. Preferable types of alkali metals and alkaline earth metals include alkali metals such as lithium, sodium and cesium, which have a low work function and a large effect of improving the electron transport ability, and alkaline earth metals such as magnesium and calcium.

In addition, since it is easy to deposit in vacuum and is excellent in handling, it is preferably in the form of a complex with an inorganic salt or an organic substance rather than a single metal. Furthermore, it is more preferable that it exists in the state of a complex with organic substance at the point of the ease of handling in air | atmosphere, and the ease of control of addition concentration. Examples of inorganic salts include oxides such as LiO and Li ₂ O, nitrides, fluorides such as LiF, NaF, and KF, Li ₂ CO ₃ , Na ₂ CO ₃ , K ₂ CO ₃ , Rb ₂ CO ₃ , Examples thereof include carbonates such as Cs ₂ CO ₃ . A preferable example of the alkali metal or alkaline earth metal is lithium from the viewpoint that the raw materials are inexpensive and easy to synthesize. Preferred examples of the organic substance in the complex with the organic substance include quinolinol, benzoquinolinol, flavonol, hydroxyimidazopyridine, hydroxybenzazole, hydroxytriazole and the like. Among these, a complex of an alkali metal and an organic substance is preferable, a complex of lithium and an organic substance is more preferable, and lithium quinolinol is particularly preferable.

  In addition, when the doping ratio of the donor compound in the electron transport layer is appropriate, the injection ratio of electrons from the cathode or the electron injection layer to the electron transport layer increases, and the cathode and the electron injection layer or the electron injection layer and the electron The energy barrier between the transport layers is reduced and the driving voltage is reduced. The suitable doping concentration varies depending on the material and the thickness of the doping region, but the molar ratio of the organic compound to the donor compound is preferably in the range of 100: 1 to 1: 100, more preferably 10: 1 to 1:10.

  The method of doping the electron transport layer with a donor compound to improve the electron transport capability is particularly effective when the thin film layer is thick. It is particularly preferably used when the total film thickness of the electron transport layer and the light emitting layer is 50 nm or more. For example, there is a method of using the interference effect to improve the light emission efficiency, but this improves the light extraction efficiency by matching the phase of the light directly emitted from the light emitting layer and the light reflected by the cathode. Is. This optimum condition varies depending on the light emission wavelength, but the total film thickness of the electron transport layer and the light-emitting layer is 50 nm or more, and in the case of long-wavelength light emission such as red, it may be a thick film near 100 nm. .

  The thickness of the electron transport layer to be doped may be part or all of the electron transport layer, but the thicker the entire electron transport layer, the higher the doping concentration. In the case of partial doping, it is desirable to provide a doping region at least at the electron transport layer / cathode interface, and the effect of lowering the voltage can be obtained only by doping in the vicinity of the cathode interface. On the other hand, when the light emitting layer is doped with the donor compound, it is desirable to provide a non-doped region at the light emitting layer / electron transport layer interface when it adversely affects the light emission efficiency.

  The method of forming each layer constituting the light emitting element is not particularly limited, such as resistance heating vapor deposition, electron beam vapor deposition, sputtering, molecular lamination method, coating method, etc., but resistance heating vapor deposition or electron beam vapor deposition is usually used in terms of element characteristics. preferable.

  The thickness of the organic layer is not limited because it depends on the resistance value of the luminescent material, but is preferably 1 to 1000 nm. The film thicknesses of the light emitting layer, the electron transport layer, and the hole transport layer are each preferably 1 nm to 200 nm, and more preferably 5 nm to 100 nm.

  The light-emitting element of the present invention has a function of converting electrical energy into light. Here, a direct current is mainly used as the electric energy, but a pulse current or an alternating current can also be used. The current value and voltage value are not particularly limited, but should be selected so that the maximum luminance can be obtained with as low energy as possible in consideration of the power consumption and lifetime of the device.

  The light emitting device of the present invention is suitably used as a display for displaying in a matrix and / or segment system, for example.

  In the matrix method, pixels for display are two-dimensionally arranged such as a lattice shape or a mosaic shape, and a character or an image is displayed by a set of pixels. The shape and size of the pixel are determined by the application. For example, a square pixel with a side of 300 μm or less is usually used for displaying images and characters on a personal computer, monitor, TV, and a pixel with a side of mm order for a large display such as a display panel. become. In monochrome display, pixels of the same color may be arranged. However, in color display, red, green, and blue pixels are displayed side by side. In this case, there are typically a delta type and a stripe type. The matrix driving method may be either a line sequential driving method or an active matrix. Although the structure of the line sequential drive is simple, the active matrix may be superior in consideration of the operation characteristics, and it is necessary to use it depending on the application.

  The segment system in the present invention is a system in which a pattern is formed so as to display predetermined information and an area determined by the arrangement of the pattern is caused to emit light. For example, the time and temperature display in a digital clock or a thermometer, the operation state display of an audio device or an electromagnetic cooker, the panel display of an automobile, and the like can be mentioned. The matrix display and the segment display may coexist in the same panel.

  The light emitting device of the present invention is also preferably used as a backlight for various devices. The backlight is used mainly for the purpose of improving the visibility of a display device that does not emit light, and is used for a liquid crystal display device, a clock, an audio device, an automobile panel, a display board, a sign, and the like. In particular, the light-emitting element of the present invention is preferably used for a backlight for a liquid crystal display device, particularly a personal computer for which a reduction in thickness is being considered, and a backlight that is thinner and lighter than conventional ones can be provided.

  EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated, this invention is not limited by these Examples. In addition, the number of the compound in each following Example points out the number of the compound described above.

Synthesis example 1
Synthesis of Compound [16] A mixed solution of 3.6 g of 1,6-dibromopyrene, 2.9 g of phenylboronic acid, 10 g of tripotassium phosphate, 54 mg of palladium acetate, 777 mg of tetrabutylammonium bromide and 100 ml of dimethylformamide was added under a nitrogen stream. The mixture was heated and stirred at 130 ° C. for 2 hours. After cooling to room temperature, 100 ml of water was poured and filtered. Washed with 50 ml of methanol. After purification by silica gel column chromatography, the solid obtained by evaporation was washed with 50 ml of methanol and vacuum-dried to obtain 3.0 g of 1,6-diphenylpyrene.

  Next, a mixed solution of 3.0 g of 1,6-diphenylpyrene, 1.5 g of N-bromosuccinimide and 84 ml of dimethylformamide was heated and stirred at 80 ° C. for 1 hour in a nitrogen stream. After cooling to room temperature, 84 ml of water was injected and filtered. Washed with 50 ml of methanol. After purification by silica gel column chromatography, the solid obtained by evaporation was washed with 50 ml of methanol and vacuum-dried to obtain 3.3 g of 3-bromo-1,6-diphenylpyrene.

  Next, 3.3 g of 3-bromo-1,6-diphenylpyrene, 1.45 g of p-chlorophenylboronic acid, 150 mg of bis (triphenylphosphine) palladium dichloride, 19 ml of 1.0 M aqueous sodium carbonate solution and 1,2-dimethoxy A mixed solution of 39 ml of ethane was stirred with heating under reflux for 3 hours under a nitrogen stream. After cooling to room temperature, 39 ml of water was poured and filtered. Washed with 50 ml of methanol. After purification by silica gel column chromatography, the solid obtained by evaporation was washed with 50 ml of methanol and vacuum-dried to obtain 3.5 g of 3- (4-chlorophenyl) -1,6-diphenylpyrene.

  Next, 3.5 g of 3- (4-chlorophenyl) -1,6-diphenylpyrene, 1.4 g of 3-pyridineboronic acid, 86 mg of bis (dibenzylideneacetone) palladium, 66 mg of tricyclohexylphosphine tetrafluoroborate, 1. A mixed solution of 10 ml of 27M tripotassium phosphate aqueous solution and 27 ml of 1,4-dioxane was heated and stirred for 4 hours under reflux in a nitrogen stream. After cooling to room temperature, 27 ml of water was poured and extracted with 50 ml of toluene. The organic layer was washed twice with 30 ml of an aqueous sodium chloride solution, dried over magnesium sulfate, evaporated and then purified by silica gel column chromatography. The solid obtained by evaporation was vacuum dried to obtain 2.3 g of a pale yellowish white solid.

The results of ¹ H-NMR analysis of the obtained powder are as follows, and it was confirmed that the pale yellowish white solid obtained above was Compound [16].
¹ H-NMR (CDCl ₃ (d = ppm)): 7.40-7.72 (11H, m), 7.74-7.81 (4H, m), 7.97-8.09 (4H, m), 8.15-8.25 (4H, m), 8.64 (1H, dd, J = 5.0 Hz, J = 1.9 Hz), 8.97 (1H, d, J = 1.9 Hz).

This compound [16] was used as a light emitting device material after sublimation purification at about 270 ° C. under a pressure of 1 × 10 ⁻³ Pa using an oil diffusion pump. The HPLC purity (area% at a measurement wavelength of 254 nm) was 99.9% before sublimation purification and 99.9% after sublimation purification.

Synthesis example 2
Synthesis of Compound [1] Pyrene 9.8 g, bis (pinacolato) diboron 27 g, [Ir (OMe) (COD)] ₂ 1.6 g, 4,4′-di-t-butyl-2,2′-bipyridyl A mixed solution of 3 g and 186 ml of degassed cyclohexane was heated and stirred at 80 ° C. for 8 hours under a nitrogen stream. After cooling to room temperature, it was evaporated. After purification by silica gel column chromatography, the solid obtained by evaporation was washed with 100 ml of hexane. After vacuum drying, 16.8 g of 2,7-bis (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) pyrene was obtained.

  Next, 2,7-bis (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) pyrene 16.8 g, iodobenzene 16.6 g, bis (triphenylphosphine) palladium A mixed solution of 130 mg of dichloride, 108 ml of 1.5M aqueous sodium carbonate solution and 185 ml of 1,2-dimethoxyethane was heated and stirred for 4 hours under reflux in a nitrogen stream. After cooling to room temperature, 185 ml of water was poured and filtered. Washed with 100 ml of methanol. After purification by silica gel column chromatography, the solid obtained by evaporation was washed with 50 ml of methanol and vacuum dried to obtain 10.5 g of 2,7-diphenylpyrene.

  Next, a mixed solution of 10.5 g of 2,7-diphenylpyrene and 600 ml of 1-methyl-2-pyrrolidone was dissolved at 80 ° C. under a nitrogen stream. After cooling to 50 ° C., 6.3 g of N-bromosuccinimide was added and stirred at room temperature for 12 hours. 1000 ml of water was injected, filtered and washed with 100 ml of methanol. After purification by silica gel column chromatography, the solid obtained by evaporation was washed with 100 ml of methanol and vacuum-dried to obtain 8.77 g of 1-bromo-2,7-diphenylpyrene.

  Next, 6.77 g of 1-bromo-2,7-diphenylpyrene, 3.66 g of p-chlorophenylboronic acid, 109 mg of bis (triphenylphosphine) palladium dichloride, 31 ml of 1.5M sodium carbonate aqueous solution and 1,2-dimethoxy A mixed solution of ethane (78 ml) was heated and stirred for 7 hours under reflux under a nitrogen stream. After cooling to room temperature, 78 ml of water was poured and filtered. Washed with 78 ml of methanol. After purification by silica gel column chromatography, the solid obtained by evaporation was washed with 50 ml of methanol. The mixture was heated and stirred with 40 ml of ethyl acetate, cooled, filtered, and washed with 50 ml of methanol. After vacuum drying, 2.5 g of 1- (4-chlorophenyl) -2,7-diphenylpyrene was obtained.

  Next, 2.5 g of 1- (4-chlorophenyl) -2,7-diphenylpyrene, 1.0 g of 3-pyridineboronic acid, 62 mg of bis (dibenzylideneacetone) palladium, 47 mg of tricyclohexylphosphine tetrafluoroborate, 1. A mixed solution of 7.2 ml of 27M tripotassium phosphate aqueous solution and 27 ml of 1,4-dioxane was heated and stirred for 6 hours under reflux in a nitrogen stream. After cooling to room temperature, 27 ml of water was poured and extracted with 150 ml of toluene. The organic layer was washed twice with 30 ml of an aqueous sodium chloride solution, dried over magnesium sulfate, evaporated and then purified by silica gel column chromatography. The solid obtained by evaporation was vacuum dried to obtain 2.3 g of a white solid.

The results of ¹ H-NMR analysis of the obtained powder are as follows, and it was confirmed that the white solid obtained above was Compound [1].
¹ H-NMR (CDCl ₃ (d = ppm)): 7.20-7.34 (4H, m), 7.37-7.47 (4H, m), 7.54-7.63 (4H, m), 7.90-8.10 (5H, m), 8.13-8.21 (2H, m), 8.28 (1H, s), 8.43 (2H, dd, J = 10.3 Hz, J = 1.6 Hz), 8.61 (2H, dd, J = 4.6 Hz, J = 1.4 Hz), 8.94 (1H, d, J = 2.2 Hz).

This compound [1] was used as a light emitting device material after sublimation purification at about 255 ° C. under a pressure of 1 × 10 ⁻³ Pa using an oil diffusion pump. The HPLC purity (area% at a measurement wavelength of 254 nm) was 99.8% before sublimation purification and 99.9% after sublimation purification.

Synthesis example 3
Synthesis of Compound [4] The compound [4] was synthesized in the same manner as in Synthesis Example 2 except that 2-bromonaphthalene was used instead of iodobenzene and 4-pyridineboronic acid was used instead of 3-pyridineboronic acid to obtain a white solid. .

The results of ¹ H-NMR analysis of the obtained powder are as follows, and it was confirmed that the white solid obtained above was Compound [4].
¹ H-NMR (CDCl ₃ (d = ppm)): 7.34 (1H, dd, J = 8.1 Hz, J = 1.6 Hz), 7.46-7.58 (8H, m), 7.63-7.68 (3H, m) , 7.79-7.82 (2H, m), 7.91-7.93 (2H, m), 8.00-8.27 (7H, m), 8.37-8.39 (2H, m), 8.57 (2H, dd, J = 10.5 Hz, J = 1.6 Hz), 8.66 (2H, dd, J = 4.3 Hz, J = 1.6 Hz).

This compound [4] was used as a light emitting device material after sublimation purification at about 330 ° C. under a pressure of 1 × 10 ⁻³ Pa using an oil diffusion pump. The HPLC purity (area% at a measurement wavelength of 254 nm) was 99.8% before sublimation purification and 99.9% after sublimation purification.

Synthesis example 4
Synthesis of Compound [6] Synthesis was performed in the same manner as in Synthesis Example 2 except that 3-quinolineboronic acid was used instead of 3-pyridineboronic acid to obtain a white solid.

The results of ¹ H-NMR analysis of the obtained powder are as follows, and it was confirmed that the white solid obtained above was Compound [6].
¹ H-NMR (CDCl ₃ (d = ppm)): 7. 24-7.37 (6H, m), 7.42-7.50 (3H, m), 7.54-7.63 (3H, m), 7.72-7.77 (3H, m ), 7.90-7.94 (3H, m), 8.01-8.22 (5H, m), 8.29 (1H, s), 8.39-8.45 (3H, m).

This compound [6] was used as a light emitting device material after sublimation purification at about 300 ° C. under a pressure of 1 × 10 ⁻³ Pa using an oil diffusion pump. The HPLC purity (area% at a measurement wavelength of 254 nm) was 99.8% before sublimation purification and 99.9% after sublimation purification.

Example 1
A glass substrate (manufactured by Geomat Co., Ltd., 11Ω / □, sputtered product) on which ITO transparent conductive film was deposited at 165 nm was cut into 38 × 46 mm and etched. The obtained substrate was ultrasonically cleaned with “Semico Clean 56” (trade name, manufactured by Furuuchi Chemical Co., Ltd.) for 15 minutes and then with ultrapure water. This substrate was subjected to UV-ozone treatment for 1 hour immediately before producing the device, placed in a vacuum deposition apparatus, and evacuated until the degree of vacuum in the apparatus became 5 × 10 ⁻⁴ Pa or less. By the resistance heating method, first, copper phthalocyanine was deposited as a hole injecting material at 10 nm, and 4,4′-bis (N- (1-naphthyl) -N-phenylamino) biphenyl was deposited as a hole transporting material at 50 nm. Next, a compound (H-1) as a host material and a compound (D-1) as a dopant material were vapor-deposited in a thickness of 40 nm on the light emitting material so that the doping concentration was 5% by weight. Next, Compound [16] was laminated to a thickness of 20 nm as an electron transport material.

Next, after depositing 0.5 nm of lithium fluoride, 1000 nm of aluminum was vapor-deposited to form a cathode, and a 5 × 5 mm square device was fabricated. The film thickness referred to here is a crystal oscillation type film thickness monitor display value. When this light emitting device was DC-driven at 10 mA / cm ² , high-efficiency blue light emission with a driving voltage of 4.6 V and an external quantum efficiency of 4.9% was obtained.

Examples 2-9
A light emitting device was fabricated in the same manner as in Example 1 except that the materials described in Table 1 were used as the host material, the dopant material, and the electron transport layer. The results of each example are shown in Table 1. In Table 1, 2E-1 is a compound shown below.

Comparative Examples 1-12
A light emitting device was fabricated in the same manner as in Example 1 except that the materials described in Table 1 were used as the host material, the dopant material, and the electron transport material. The results of each comparative example are shown in Table 1. In Table 1, E-1 to E-4 are the compounds shown below.

Examples 10-23, Comparative Examples 13-15
A light emitting device was fabricated in the same manner as in Example 1 except that the materials described in Table 2 were used as the host material, the dopant material, and the electron transport layer. The results of each example and comparative example are shown in Table 2. In Table 2, H-2 to H-8 and D-2 to D-10 are the compounds shown below.

Example 24
A glass substrate (manufactured by Geomat Co., Ltd., 11Ω / □, sputtered product) on which ITO transparent conductive film was deposited at 165 nm was cut into 38 × 46 mm and etched. The obtained substrate was ultrasonically cleaned with “Semico Clean 56” (trade name, manufactured by Furuuchi Chemical Co., Ltd.) for 15 minutes and then with ultrapure water. This substrate was subjected to UV-ozone treatment for 1 hour immediately before producing the device, placed in a vacuum deposition apparatus, and evacuated until the degree of vacuum in the apparatus became 5 × 10 ⁻⁴ Pa or less. First, 1,4,5,8,9,12-hexaazatriphenylenehexacarbonitrile is used as the hole injecting material by the resistance heating method, and 4,4'-bis (N- (1 -Naphthyl) -N-phenylamino) biphenyl was deposited by 50 nm. Next, a compound (H-1) as a host material and a compound (D-2) as a dopant material were vapor-deposited on the light-emitting material to a thickness of 40 nm so that the doping concentration was 5% by weight. Next, a layer obtained by mixing the compound [16] and the donor compound (2E-1: lithium quinolinol) at a deposition rate ratio of 1: 1 (= 0.05 nm / s: 0.05 nm / s) was used as an electron transport layer. Laminated to thickness.

Next, after depositing 1 nm of lithium quinolinol, a co-deposited film of magnesium and silver was deposited at a deposition rate ratio of magnesium: silver = 10: 1 (= 0.5 nm / s: 0.05 nm / s) to 100 nm to form a cathode, A 5 × 5 mm square element was produced. The film thickness referred to here is a crystal oscillation type film thickness monitor display value. When this light emitting device was DC-driven at 10 mA / cm ² , high-efficiency blue light emission with a driving voltage of 3.7 V and an external quantum efficiency of 5.6% was obtained.

Examples 25-28
A light emitting device was produced in the same manner as in Example 24 except that the materials described in Table 3 were used as the host material, the dopant material, and the electron transport layer. The results of each example are shown in Table 3.

Claims (7)

A light-emitting element material comprising a pyrene compound represented by the general formula (1).

(R ^{1 to} R ⁴ may be the same as or different from each other, hydrogen, alkyl group, cycloalkyl group, heterocyclic group, alkenyl group, cycloalkenyl group, alkynyl group, alkoxy group, alkylthio group, aryl ether group, aryl thioether group, an aryl group, a heteroaryl group, halogen, a carbonyl group, a carboxyl group, an oxycarbonyl group, a carbamoyl group, an amino group, a silyl group, and -P (= ^O) .R selected from the group consisting of R 5 ^{R 6 5} And R ⁶ represents an aryl group or a heteroaryl group, and adjacent substituents may form a ring, L is an arylene group, and HAr is an aromatic heterocyclic group containing an electron-accepting nitrogen. X ^{1 to} X ⁵ satisfy any of the following (A) to (D).
(A) X ² and X ³ and X ⁵ are hydrogen, and X ¹ and X ⁴ are aryl groups.
(B) X ¹ and X ³ and X ⁴ are hydrogen, and X ² and X ⁵ are aryl groups.
(C) X ¹ and X ⁴ and X ⁵ are hydrogen, and X ² and X ³ are aryl groups.
(D) X ¹ and X ² and X ⁴ are hydrogen, and X ³ and X ⁵ are aryl groups.
However, X ^{1 to} X ⁵ do not include an anthracene skeleton and a pyrene skeleton. ) A light emitting device in which at least a light emitting layer and an electron transport layer are present between an anode and a cathode and emits light by electric energy, wherein the electron transport layer contains the light emitting device material according to claim 1. . The light emitting device according to claim 2, further comprising a donor compound in the electron transport layer. The donor compound is an alkali metal, an inorganic salt containing an alkali metal, a complex of an alkali metal and an organic substance, an alkaline earth metal, an inorganic salt containing an alkaline earth metal, or a complex of an alkaline earth metal and an organic substance Item 4. A light emitting device according to Item 3. 4. The light emitting device according to claim 3, wherein the donor compound is a complex of an alkali metal and an organic substance or a complex of an alkaline earth metal and an organic substance. The light emitting device according to claim 2, wherein the light emitting layer contains a phosphorescent material. A light emitting device having at least a light emitting layer between an anode and a cathode and emitting light by electrical energy, wherein the light emitting layer contains the light emitting device material according to claim 1.