JPH09268283A - Luminescent material for organic electroluminescence element and organic electroluminescent element using the same - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a luminescent material for organic electroluminescent elements which can attain high intensity and high luminous efficiency with high reliability and reduced luminescent deterioration and to provide an organic electroluminescent element using the same. SOLUTION: This luminescent material for an organic electroluminescent element is represented by the formula (A to B are each an alkyl group, a monocyclic group, a condensed ring group; A and B or C and D are incorporated to form a heterocyclic ring group having a nitrogen atom as a binder). A luminescent layer or an organic thin layers containing the luminescent layer is formed between a couple of electrodes to provide the objective organic electroluminescence element.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a light emitting material for an organic electroluminescence (EL) element used for a flat light source or a display and a high brightness light emitting element.

[0002]

2. Description of the Related Art An EL device using an organic substance is expected to be used as an inexpensive, large-area, full-color display device of a solid light emitting type, and many developments have been made. Generally EL
Is composed of a light-emitting layer and a pair of opposed electrodes sandwiching the layer. In light emission, when an electric field is applied between both electrodes, electrons are injected from the cathode side and holes are injected from the anode side. Further, the electrons are recombined with holes in the light emitting layer, and energy is emitted as light when the energy level returns from the conduction band to the valence band.

[0003] Conventional organic EL devices have a higher driving voltage and lower luminous brightness and luminous efficiency than inorganic EL devices.
In addition, the characteristic deterioration was remarkable, and it had not been put to practical use.
2. Description of the Related Art In recent years, an organic EL in which a thin film containing an organic compound having high fluorescence quantum efficiency that emits light at a low voltage of 10 V or less is laminated.
Devices have been reported and are of interest (see Applied Physics Letters, vol. 51, p. 913, 1987). This method uses a metal chelate complex as a light emitting layer and an amine compound as a hole injecting layer to obtain high-luminance green light emission, which can be driven by a DC voltage of 6 to 7 V, and the maximum light emission luminance is It has several thousand (cd / m ² ) and maximum luminous efficiency of 1.5 (lm / W), which is close to the practical range.

[0004] However, organic EL devices up to now have improved luminous intensity due to the improved structure, but do not yet have sufficient luminous brightness. In addition, there is a major problem that the stability upon repeated use is poor. This is because, for example, a metal chelate complex such as tris (8-hydroxyquinolinato) aluminum complex (Alq3) is
It was chemically unstable at the time of electroluminescence, had poor adhesion to the cathode, and was greatly deteriorated by light emission for a short time.

As a blue light emitting material for an organic EL device, a material having a skeleton such as anthracene, tetraphenylbutadiene, stilbene, bisstyryl, cyclopentadiene, oxadiazole has been proposed. Etc. are not enough, and there is a big problem in practical use (edited by the Next Generation Device Study Group, “Organic EL
Device development strategy ”Science Forum Inc., 1
69, 1992). For the above reasons, in order to develop an organic EL element having a large emission brightness and capable of emitting light with a long life, it is desired to develop a light emitting material having excellent light emitting ability and durability.

[0006]

DISCLOSURE OF THE INVENTION The present invention provides an organic EL device having high emission brightness and long emission life. As a result of intensive studies by the present inventors, the organic EL device using the light emitting material for organic EL device represented by the general formula [1] or the general formula [2] in the light emitting layer has high emission brightness and long emission life. They have found the present invention and completed the present invention.

[0007]

The present invention relates to a luminescent material for an organic electroluminescence device represented by the following general formula [1]. General formula [1]

Embedded image [In the formula, A to D are a substituted or unsubstituted alkyl group, a substituted or unsubstituted monocyclic group, a substituted or unsubstituted condensed polycyclic group, A and B or C and D are integrated into a nitrogen atom. Represents a heterocyclic group having a bond. ]

Further, the present invention is a light emitting material for an organic electroluminescence device, wherein A to D in the general formula [1] are substituted or unsubstituted monocyclic groups.

Further, the present invention is a light emitting material for an organic electroluminescence device represented by the following general formula [2]. General formula [2]

Embedded image [Wherein, R ^{1 to} R ²³ are each independently a hydrogen atom, a halogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted amino group, a substituted or unsubstituted It represents a monocyclic group or a substituted or unsubstituted fused polycyclic group. X ^{1 to} X ⁴ are each independently a direct bond, —O—, —S—,>C═O,> SO ₂ ,
_{- (CH 2) X -O- (} CH 2) y - ( wherein, x and y is each independently represent a positive integer from 0 to 20,
x + y = 0 never occurs. ), -P-,> P = O,
> SiR ²¹ (R ²² ), NR ²³ , a substituted or unsubstituted alkylene group, or a substituted or unsubstituted aliphatic ring residue. ]

The present invention further provides an organic electroluminescent device comprising a light emitting layer or a plurality of organic compound thin films including the light emitting layer formed between a pair of electrodes, wherein the light emitting layer is the above light emitting material for an organic electroluminescent device. It is an organic electroluminescence element which is a layer to be contained.

The present invention further provides a layer containing an aromatic tertiary amine derivative and / or a phthalocyanine derivative,
The above organic electroluminescent element is formed between the light emitting layer and the anode.

The present invention further provides a metal complex compound and / or
Alternatively, the organic electroluminescence element is the above-mentioned organic electroluminescence element formed by forming a layer containing a nitrogen-containing five-membered ring derivative between the light emitting layer and the cathode.

BEST MODE FOR CARRYING OUT THE INVENTION

Examples of the alkyl group represented by A to D or the compound represented by the general formula [2] of the formula [1] include a methyl group, an ethyl group, a propyl group, a butyl group, a sec-butyl group and a ter.
t-butyl group, pentyl group, hexyl group, heptyl group,
C1-C1 such as octyl, stearyl and benzyl
There are 20 linear and branched alkyl groups.

As the alkylene group of the general formula [2], a methylene group, an ethylene group, a propylene group, a butylene group, s
There are linear and branched alkylene groups having 1 to 20 carbon atoms such as ec-butylene group, tert-butylene group, pentylene group, hexylene group, heptylene group, octylene group and stearylene group.

The monocyclic group A to D of the compound of the general formula [1] or the monocyclic group of the general formula [2] is a monocyclic cycloalkyl group,
Examples include monocyclic aryl groups and monocyclic heterocyclic groups. Examples of the monocyclic cycloalkyl group include a cycloalkyl group having 4 to 8 carbon atoms such as a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, and a cyclooctyl group.

The monocyclic aryl group includes a phenyl group. The monocyclic heterocyclic group, thionyl group, thiophenyl group, furanyl group, pyrrolyl group, imidazolyl group, pyrazolyl group, pyridyl group, pyrazinyl group, pyrimidyl group, pyridazinyl group, oxazolyl group, thiazolyl group, oxadiazolyl group, thiadiazolyl group, There are imidazolyl groups and the like.

Examples of the condensed polycyclic group A to D of the compound of the general formula [1] or the condensed polycyclic group of the general formula [2] include a condensed polycyclic aryl group, a condensed polycyclic heterocyclic group and a condensed polycyclic cycloalkyl group. . Examples of the condensed polycyclic aryl group include a naphthyl group, anthranyl group, phenanthrenyl group, fluorenyl group, acenaphthyl group, azulenyl group, heptalenyl group, acenaphthylenyl group and pyrenyl group.

Examples of the condensed polycyclic heterocyclic group include indolyl group, quinolyl group, isoquinolyl group, phthalazinyl group, quinoxalanyl group, quinazolinyl group, carbazolyl group, acridinyl group, phenazinyl group, furfuryl group, isothiazolyl group, isoxazolyl group and flazanyl group. , Phenoxazinyl group, benzoxazolyl group, benzothiazolyl group, benzimidazolyl group and the like.

A substituent for the above alkyl group, monocyclic group, condensed polycyclic group, or a heterocyclic group having a nitrogen atom in which A and B or C and D are integrated as a bond, or the general formula [2]
R ^{1 to} R ²⁰ of the compound represented by are as follows. As a halogen atom, fluorine, chlorine, bromine, iodine. As a substituted or unsubstituted alkyl group, a methyl group, an ethyl group, a propyl group, a butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a stearyl group, a trichloromethyl group, Trifluoromethyl group, cyclopropyl group, cyclohexyl group, 1,3-cyclohexadienyl group, 2-cyclopenten-1-yl group, 2,4-cyclopentadiene-1-yridenyl group, benzyl group, dimethylbenzyl group, di (Trifluoromethyl) benzyl group and the like.

Examples of the substituted or unsubstituted alkoxy group include methoxy group, ethoxy group, propoxy group, n-butoxy group, tert-butoxy group, pentyloxy group, hexyloxy group, stearyloxy group and trifluoromethoxy group. Examples of the substituted or unsubstituted thioalkoxy groups include methylthio, ethylthio, propylthio, butylthio, sec-butylthio, tert-butylthio, pentylthio, hexylthio, heptylthio, octylthio, and the like.

As the mono- or di-substituted amino group, methylamino group, dimethylamino group, ethylamino group, diethylamino group, dipropylamino group, dibutylamino group, phenylmethylamino group, diphenylamino group, ditolylamino group, dibenzylamino group. Group, bis (acetoxymethyl) amino group, bis (acetoxyethyl) amino group, bis (acetoxypropyl) amino group and the like.

Examples of the substituted or unsubstituted aryloxy group include phenoxy group, p-tert-butylphenoxy group, 4-methylphenoxy group and the like. As the substituted or unsubstituted arylthio group, phenylthio group, 4-methylphenylthio group and the like.

Examples of the substituted or unsubstituted aryl group include a phenyl group, a biphenyl group, a terphenyl group and 4-
Methylthiophenyl group, 3,5-dicyanophenyl group,
o-, m-, p-tolyl group, xylyl group, o-, m-,
p-cumenyl group, 4-benzylphenyl group, 4-dimethylbenzyl group, mesityl group, pentalenyl group, indenyl group, naphthyl group, azulenyl group, heptalenyl group, acenaphthylenyl group, phenanthrenyl group, fluorenyl group, anthryl group, anthraquinolyl group. , 3-methylanthryl group, triphenylyl group, pyrenyl group, chrysenyl group, picenyl group, perylenyl group, pentaphenyl group,
Pentacenyl group, tetraphenylenyl group, hexaphenyl group, hexacenyl group, rubicenyl group, coronenyl group,
Trinaphthylenyl group, heptaphenyl group, heptaenyl group, pyrantrenyl group, ovarenyl group and the like.

As the substituted or unsubstituted heterocyclic group, thionyl group, thiophenyl group, furanyl group, pyrrolyl group,
Imidazolyl group, pyrazolyl group, pyridyl group, pyrazinyl group, pyrimidyl group, pyridazinyl group, indolyl group,
Quinolyl group, isoquinolyl group, phthalazinyl group, quinoxalanyl group, quinazolinyl group, carbazolyl group, acridinyl group, phenazinyl group, furfuryl group, isothiazolyl group, isoxazolyl group, flazanyl group, phenoxazinyl group, benzoxazolyl group, benzothiazolyl group, benzimidazolyl group , 2-methylpyridyl group, 3
-Cyanopyridyl group, oxazolyl group, thiazolyl group,
Oxadiazolyl group, thiadiazolyl group, imidazolyl group, etc.

In particular, the general formula [1] or the general formula [2]
Among the compounds represented by, the compounds having a substituent having an aromatic ring or forming an aromatic ring with each other have a high glass transition temperature and a high melting point temperature, and When used as a light emitting material for an element, it exhibits high emission brightness and is advantageous against deterioration of the element due to Joule heat even when emitting light for a long time. The compounds of the present invention are not limited to these substituents.

An example of a method for synthesizing the compound represented by the general formula [1] or the general formula [2] of the present invention is shown below.

9,10-bis (4-halogenophenyl)
A diamine derivative which may have an anthracene and a substituent,
Alternatively, 9,10-bis (4-aminophenyl) anthracene and a halogenated derivative which may have a substituent are reacted with a base and a catalyst in a solvent to give a compound represented by the general formula [1] or the general formula [2]. ] Compound is synthesized. It can also be synthesized from an anthraquinone derivative instead of the anthracene derivative. As the base, potassium carbonate, sodium carbonate, potassium hydroxide, sodium hydroxide, aqueous ammonia or the like can be used. As the catalyst, copper powder, cuprous chloride, tin, stannous chloride,
There are pyridine, aluminum trichloride or titanium tetrachloride. The solvent is nitrobenzene, dimethylformamide,
1,3-dimethyl-2-imidazolidinone, benzene,
Any high boiling point solvent such as toluene or xylene may be used.

Typical examples of the compounds of the present invention are shown in Table 1 below, but the present invention is not limited to these representative examples.

[0029]

[Table 1]

[0030]

[0031]

[0032]

[0033]

[0034]

[0035]

[0036]

[0037]

[0038]

The compound represented by the general formula [1] or the general formula [2] of the present invention is a compound which has little concentration quenching of light emission in the solid state and is stable even when an electric field is applied. Excellent as a light emitting material. Further, it has a good hole injecting property and can be effectively used as a hole transporting type light emitting material. In addition, in the light emitting layer, other hole injection material,
An electron injection material, a light emitting material or a doping material may be used.

The organic EL device is a device in which a single or multilayer organic thin film is formed between an anode and a cathode. In the case of the single layer type, a light emitting layer is provided between the anode and the cathode. The light emitting layer contains a light emitting material and may further contain a hole injection material or an electron injection material for transporting holes injected from an anode or electrons injected from a cathode to the light emitting material. The multilayer type includes (anode / hole injection layer / electron injection layer / cathode), (anode / hole injection layer / electron injection layer / cathode), and (anode / hole injection layer / light emission layer / electron injection layer / cathode) multilayer. There is an organic EL element stacked in a configuration. The compounds of the general formula [1] and the general formula [2] can be used in the light emitting layer as effective light emitting materials.

In the light emitting layer, if necessary, in addition to the compound of the general formula [1] or the general formula [2] of the present invention, a further light emitting material, a doping material, a hole injecting material or an electron injecting material is used. You can also do it. When the organic EL element has a multilayer structure, it is possible to prevent a decrease in luminance and life due to quenching. If necessary, luminescent material,
A doping material, a hole injection material and an electron injection material can be used in combination. Further, it is possible to improve the light emission brightness and the light emission efficiency and obtain light emission from blue to red by using the doping material. Further, each of the hole injection layer, the light emitting layer, and the electron injection layer may be formed in a layer structure of two or more layers.

As the conductive material used for the anode of the organic EL element, one having a work function larger than 4 eV is suitable, and carbon, aluminum, vanadium, iron, cobalt, nickel, tungsten, silver, gold, platinum. , Palladium and their alloys, metal oxides such as tin oxide and indium oxide used for ITO substrates and NESA substrates,
Further, an organic conductive resin such as polythiophene or polypyrrole is used.

The conductive material used for the cathode is 4
Those having a work function smaller than eV are suitable, and magnesium, calcium, tin, lead, titanium, yttrium, lithium, ruthenium, manganese and the like and alloys thereof are used. As an alloy, magnesium-
Examples thereof include, but are not limited to, silver, magnesium-indium, lithium-aluminum, and the like. The anode and the cathode may be formed of two or more layers if necessary.

In the organic EL device, it is desirable that at least one of them is sufficiently transparent in the emission wavelength region of the device in order to emit light efficiently. Further, it is desirable that the substrate is also transparent. The transparent electrode is set using the above-described conductive material so as to secure a predetermined translucency by a method such as vapor deposition or sputtering. The electrode on the light emitting surface desirably has a light transmittance of 10% or more. The substrate is not limited as long as it has mechanical and thermal strength and is transparent, but examples thereof include a glass substrate, a transparent resin such as polyethylene, polyether sulfone, and polypropylene.

For forming each layer of the organic EL element according to the present invention, any method of dry film forming method such as vacuum deposition, sputtering, ion plating or wet film forming method such as spin coating or dipping may be applied. You can The film thickness is not particularly limited, but each layer needs to be set to an appropriate film thickness. If the film thickness is too thick, a large applied voltage is required to obtain a constant light output, resulting in poor efficiency. If the film thickness is too small, pinholes and the like are generated, and sufficient light emission luminance cannot be obtained even when an electric field is applied. The normal film thickness is suitable in the range of 5 nm to 10 μm,
The range of 10 nm to 0.2 μm is more preferable.

In the case of the wet film forming method, the materials for forming the respective layers are ethanol, chloroform, tetrahydrofuran,
The thin film is formed by dissolving or dispersing in a suitable solvent such as dioxane, and any solvent may be used. In any of the organic thin film layers, a suitable resin or additive may be used for improving film forming properties, preventing pinholes in the film, and the like. Resins that can be used include insulating resins such as polystyrene, polycarbonate, polyarylate, polyester, polyamide, polyurethane, polysulfone, polymethylmethacrylate, polymethylacrylate, and cellulose, and photoconductive materials such as poly-N-vinylcarbazole and polysilane. Examples of the resin include conductive resins such as polythiophene and polypyrrole. Examples of the additive include an antioxidant, an ultraviolet absorber, and a plasticizer.

The present organic EL device comprises a light emitting layer, a hole injection layer,
In the electron injection layer, known light emitting materials, doping materials, hole injection materials and electron injection materials can be used if necessary.

As the light emitting material or the doping material which can be used in the light emitting layer together with the compound of the general formula [1], anthracene, naphthalene, phenanthrene, pyrene, tetracene, coronene, chrysene, fluorescein, perylene, phthaloperylene, naphthaloperylene, perinone, phthaloperinone, Naphthaloperinone, diphenylbutadiene, tetraphenylbutadiene, coumarin, oxadiazole, aldazine, bisbenzoxazoline, bisstyryl, pyrazine, cyclopentadiene, quinoline metal complex, aminoquinoline metal complex, benzoquinoline metal complex, imine, diphenylethylene, vinylanthracene , Diaminocarbazole, pyran, thiopyran, polymethine, merocyanine, imidazole chelated oxinoid compounds, quinacry Emissions, rubrene, benzidine type triphenylamine, styrylamine type triphenylamine, there is a diamine-type triphenylamine and known fluorescent dyes such as, but not limited thereto.

The hole-injecting material has the ability to transport holes, has the effect of injecting holes from the anode, and has an excellent effect of injecting holes into the light-emitting layer or the light-emitting material. Examples thereof include compounds that prevent excitons from moving to the electron injection layer or the electron injection material and have excellent thin film forming ability. Specifically, phthalocyanine derivatives, naphthalocyanine derivatives, porphyrin derivatives, oxazole, oxadiazole, triazole, imidazole, imidazolone, imidazolethione, pyrazoline, pyrazolone,
Tetrahydroimidazole, oxazole, oxadiazole, hydrazone, acylhydrazone, polyarylalkane, stilbene, butadiene, benzidine-type triphenylamine, styrylamine-type triphenylamine, diamine-type triphenylamine, and derivatives thereof, and polyvinyl carbazole , Polysilane, and a polymer material such as a conductive polymer, but are not limited thereto.

In the organic EL device of the present invention, a more effective hole injection material is an aromatic tertiary amine derivative or a phthalocyanine derivative. Specifically, examples of the aromatic tertiary amine derivative include triphenylamine, tolylamine, tolylphenylamine, N, N′-diphenyl-N, N ′-(3-methylphenyl) -1,1 ′.
-Biphenyl-4,4'-diamine, N, N, N'N '
-(4-methylphenyl) -1,1′-phenyl-4,
4′-diamine, N, N, N′N ′-(4-methylphenyl) -1,1′-biphenyl-4,4′-diamine,
N, N'-diphenyl-N, N'-dinaphthyl-1,
1'-biphenyl-4,4'-diamine, N, N'-
(Methylphenyl) -N, N ′-(4-n-butylphenyl) -phenanthrene-9,10-diamine, N, N
Examples include, but are not limited to, -bis (4-di-4-tolylaminophenyl) -4-phenyl-cyclohexane and the like, and oligomers and polymers having an aromatic tertiary amine skeleton. As phthalocyanine (Pc) derivatives, H ₂ Pc, CuPc, C
oPc, NiPc, ZnPc, PdPc, FePc, M
nPc, ClAlPc, ClGaPc, ClInPc,
ClSnPc, Cl ₂ SiPc, (HO) AlPc,
(HO) GaPc, VOPc, TiOPc, MoOP
c, a phthalocyanine derivative such as GaPc-O-GaPc, a naphthalocyanine derivative, and the like, but are not limited thereto.

The electron injecting material has an ability to transport electrons, has an electron injecting effect from the cathode, and an excellent electron injecting effect to the light emitting layer or the light emitting material. A compound that prevents migration to the hole injection layer and has an excellent thin film forming ability can be mentioned. For example, fluorenone, anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, fluorenylidenemethane, anthraquinodimethane,
There are, but not limited to, anthrone, a metal complex compound and the like and their derivatives. It is also possible to sensitize by adding an electron accepting material to the hole injecting material and an electron donating material to the electron injecting material.

In the organic EL device of the present invention, a more effective electron injection material is a metal complex compound or a nitrogen-containing five-membered ring derivative. Specifically, as the metal complex compound, lithium 8-hydroxyquinolinate, bis (8
-Hydroxyquinolinato) zinc, bis (8-hydroxyquinolinato) copper, bis (8-hydroxyquinolinato) manganese, tris (8-hydroxyquinolinato)
Aluminum, tris (2-methyl-8-hydroxyquinolinato) aluminum, tris (8-hydroxyquinolinato) gallium, bis (10-hydroxybenzo [h] quinolinato) beryllium, bis (10-hydroxybenzo [h] (Quinolinato) zinc, bis (2-methyl-8-quinolinato) chlorogallium, bis (2-methyl-8-quinolinato) (o-cresolate) gallium, bis (2-methyl-8-quinolinato) (1-naphtholate) aluminum , Bis (2-methyl-8-quinolinato) (2-naphtholate) gallium and the like,
It is not limited to these. As the nitrogen-containing five-membered derivative, an oxazole, thiazole, oxadiazole, thiadiazole or triazole derivative is preferable. Specifically, 2,5-bis (1-phenyl)
-1,3,4-oxazole, dimethyl POPOP,
2,5-bis (1-phenyl) -1,3,4-thiazole, 2,5-bis (1-phenyl) -1,3,4-oxadiazole, 2- (4′-tert-butylphenyl) ) -5- (4 "-biphenyl) 1,3,4-oxadiazole, 2,5-bis (1-naphthyl) -1,3,4
-Oxadiazole, 1,4-bis [2- (5-phenyloxadiazolyl)] benzene, 1,4-bis [2-
(5-phenyloxadiazolyl) -4-tert-butylbenzene], 2- (4'-tert-butylphenyl) -5- (4 "-biphenyl) -1,3,4-thiadiazole, 2,5- Bis (1-naphthyl) -1,3,4
-Thiadiazole, 1,4-bis [2- (5-phenylthiadiazolyl)] benzene, 2- (4'-tert-
(Butylphenyl) -5- (4 "-biphenyl) -1,
3,4-triazole, 2,5-bis (1-naphthyl)
-1,3,4-triazole, 1,4-bis [2- (5
-Phenyltriazolyl)] benzene and the like, but are not limited thereto.

In the present organic EL device, in addition to the compound of the general formula [1] or the general formula [2], at least one of a light emitting material, a doping material, a hole injection material and an electron injection material is contained in the same layer. May be. In order to improve the stability of the organic EL device obtained according to the present invention with respect to temperature, humidity, atmosphere, etc., a protective layer is provided on the surface of the device, or silicon oil or the like is sealed to protect the entire device. It is also possible.

As described above, in the present invention, since the compound of the general formula [1] or the general formula [2] is used for the organic EL device, the luminous efficiency and the luminous brightness can be increased. In addition, this device is extremely stable against heat and current, and furthermore, it can obtain a practically usable light emission brightness at a low driving voltage.
The deterioration, which was a big problem until now, could be greatly reduced.

The organic EL element of the present invention can be used as a flat panel display such as a wall-mounted television or a flat light emitting body.
It is applied to light sources such as copiers and printers, light sources such as liquid crystal displays and instruments, display boards, and marker lights, and its industrial value is extremely large.

The material of the present invention can also be used in the fields of organic EL devices, electrophotographic photoreceptors, photoelectric conversion devices, solar cells, image sensors and the like.

[0057]

EXAMPLES The present invention will be described in detail below based on examples. The term "parts" in this example means "parts by weight".

Method for synthesizing compound (3) In 30 parts of nitrobenzene, 7.9 parts of 9,10-bis (4-bromophenyl) anthracene, 5.5 parts of N-phenylbenzylamine, 4 parts of potassium carbonate and copper powder. 0.5 part was added, and the mixture was stirred under a nitrogen atmosphere at 205 ° C. for 15 hours. Then, the obtained brown solid was extracted with toluene, concentrated, purified by column chromatography using silica gel, and recrystallized with n-hexane to obtain 3.8 parts of a powder having yellow-green fluorescence. Obtained. As a result of molecular weight analysis, it was confirmed to be compound (3). The results of elemental analysis of the product are shown below. Elemental analysis result Calculated as C ₅₂ H ₄₀ N ₂ (%): C: 90.14 H: 5.82 N: 4.04 Experimental value (%): C: 90.26 H: 5.95 N: 3 .79

Method for synthesizing compound (5) In 100 parts of 1,3-dimethyl-2-imidazolidinone, 18 parts of 9,10-bis (4-aminophenyl) anthracene, 101 parts of iodobenzene, and cuprous chloride 0.5
And 22 parts of potassium hydroxide were added, and the mixture was added at 205 ° C. for 3 days.
Stirred for 0 hours. Then, it was diluted with 500 parts of water, filtered and washed with water. Then, extraction with toluene, concentration, and purification by column chromatography using silica gel to obtain 21 parts of a powder having blue fluorescence. As a result of molecular weight analysis, it was confirmed to be compound (5). The results of elemental analysis of the product are shown below. Elemental analysis result Calculated value (%) as C ₅₀ H ₃₆ N ₂ : C: 90.37 H: 5.42 N: 4.21 Experimental value (%): C: 90.49 H: 5.53 N: 3 .98 The infrared absorption spectrum (KBr tablet method) of this compound is shown in FIG.

Method for synthesizing compound (6) In 50 parts of 1,3-dimethyl-2-imidazolidinone,
9,10-bis (4-aminophenyl) anthracene 1
5 parts, m-iodotoluene 150 parts, cuprous chloride 0.5
And 20 parts of potassium hydroxide were added to the mixture at 205 ° C. for 3 days.
Stirred for 0 hours. Then, it was diluted with 500 parts of water, filtered and washed with water. Then, extraction with toluene, concentration, and purification by column chromatography using silica gel to obtain 25 parts of a powder having blue fluorescence. As a result of molecular weight analysis, it was confirmed to be Compound (6). The results of elemental analysis of the product are shown below. Elemental analysis result Calculated value (%) as C ₅₄ H ₄₄ N ₂ : C: 89.96 H: 6.15 N: 3.89 Experimental value (%): C: 90.05 H: 6.21 N: 3 .74 The infrared absorption spectrum (KBr tablet method) of this compound is shown in FIG.

Method for synthesizing compound (7) In 20 parts of nitrobenzene, 8.9 parts of 9,10-bis (4-iodophenyl) anthracene, 5.9 parts of 4,4-dimethyl-diphenylamine, 4 parts of potassium carbonate, 0.5 part of copper powder was added, and the mixture was stirred at 205 ° C. for 10 hours in a nitrogen atmosphere. Then, the obtained brown solid was extracted with toluene, concentrated, purified by column chromatography using silica gel, and recrystallized with n-hexane to obtain 3.5 parts of a powder having blue-green fluorescence. Obtained. As a result of molecular weight analysis, it was confirmed to be compound (7). The results of elemental analysis of the product are shown below. Elemental analysis result Calculated value (%) as C ₅₄ H ₄₄ N ₂ : C: 89.96 H: 6.15 N: 3.89 Experimental value (%): C: 89.90 H: 6.23 N: 3 .87 The infrared absorption spectrum (KBr tablet method) of this compound is shown in FIG.

Method for synthesizing compound (24) In 30 parts of nitrobenzene, 8.9 parts of 9,10-bis (4-iodophenyl) anthracene, 12.2 parts of 4,4-diisopropyl (2-phenyl) diphenylamine,
4 parts of potassium carbonate and 0.5 part of copper powder were added, and the mixture was stirred at 205 ° C. for 15 hours in a nitrogen atmosphere. Then, the obtained brown solid is extracted with toluene, concentrated, purified by column chromatography using silica gel, recrystallized with n-hexane, and a powder 4.8 having yellow-green fluorescence is obtained.
Got a part. As a result of molecular weight analysis, it was confirmed to be compound (24). The results of elemental analysis of the product are shown below. Elemental analysis C ₈₆ H ₇₆ N ₂ Calculated (%): C: 90.81 H : 6.73 N: 2.46 Found (%): C: 90.95 H : 6.82 N: 2 .77

Example 1 Compound (7) was added onto a washed glass plate with an ITO electrode.
2,5-bis (1-naphthyl) -1,3,4-oxadiazole and polycarbonate resin (Teijin Kasei: Panlite K-1300) are dissolved in tetrahydrofuran at a ratio of 2: 3: 5, and spin coating is performed. 10
A light emitting layer of 0 nm was obtained. An electrode having a thickness of 150 nm was formed thereon with an alloy of magnesium and silver mixed at a ratio of 10: 1 to obtain an organic EL device. This device has an emission luminance of 90 (cd / m ² ) at a DC voltage of 5 V and a maximum emission luminance of 7500.
Blue light emission of (cd / m ² ) and a luminous efficiency of 0.7 (lm / W) was obtained.

Example 2 Compound (9) was dissolved in methylene chloride on a washed glass plate with an ITO electrode, and a light emitting layer having a thickness of 50 nm was obtained by spin coating. Then, tris (8-hydroxyquinolinato) aluminum complex (Alq3)
Was vacuum-deposited to form an electron injection layer having a film thickness of 30 nm, and an electrode having a film thickness of 100 nm was formed on the electron injection layer having a thickness of 10: 1 to form an organic EL device.
The hole injection layer and the light emitting layer are formed in a vacuum of 10 ^-6 Torr,
The deposition was performed at a substrate temperature of room temperature. This device has a light emission brightness of 200 (cd / m ² ) at a DC voltage of 5 V, a maximum light emission brightness of 13000 (cd / m ² ), and a light emission efficiency of 1.2 (lm / m ² ).
Blue light emission of W) was obtained.

Example 3 Compound (41) was applied onto a washed glass plate with an ITO electrode.
Was vacuum-deposited to form a hole injection layer having a film thickness of 40 nm. Then, the compound (24) is vacuum-deposited to a film thickness of 40 n.
m light emitting layer is formed, and also Alq3 is vacuum-deposited,
An electron injection layer having a film thickness of 40 nm was formed. On top of that, an alloy of magnesium and silver mixed at a ratio of 10: 1 with a film thickness of 100 n
An electrode of m was formed to obtain an organic EL device. Each thin film layer is
Deposition was performed under the conditions of a substrate temperature of room temperature in a vacuum of 10 ⁻⁶ Torr. This device has a light emission luminance of 380 at a DC voltage of 5V.
(Cd / m ² ), maximum emission brightness 18500 (cd /
m ² ), and blue light emission with a luminous efficiency of 1.9 (lm / W) was obtained.

[0066]

Embedded image Compound (41)

Examples 4 to 43 A compound (42) represented by the following chemical structure was vacuum-deposited on a washed glass plate with an ITO electrode to give a film thickness of 40 nm.
Was obtained. Next, the compounds shown in Table 2 were vacuum-deposited as light-emitting materials to obtain a light-emitting layer having a thickness of 40 nm. Further, a compound (18) represented by the following chemical structure is vacuum-deposited to form an electron injection layer having a thickness of 40 nm, and an alloy in which magnesium and silver are mixed at a ratio of 10: 1 has a thickness of 150 nm.
An electrode having a thickness of nm was formed to obtain an organic EL device. Each layer was vapor-deposited under a vacuum of 10 ⁻⁶ Torr and a substrate temperature of room temperature. Table 2 shows the light emission characteristics of this device. The light emission luminance in Table 2 is the luminance when a DC voltage of 5 V was applied, and all the organic EL elements of this example were blue light emitting elements with high light emission efficiency.

[0068]

[Chemical 6] Compound (42)

[0069]

Embedded image Compound (43)

[0070]

[Table 2]

[0071]

Example 44 Compound (42) was placed on a washed glass plate with an ITO electrode.
Was vacuum-deposited to obtain a hole injection layer having a thickness of 40 nm. Then, the compound (25) was vacuum-deposited as a light emitting material to obtain a light emitting layer having a film thickness of 40 nm. Further, 2,5-bis (1
-Naphthyl) -1,3,4-oxadiazole was vacuum-deposited to obtain an electron injection layer having a film thickness of 40 nm. in addition,
An alloy of magnesium and silver mixed at a ratio of 10: 1 with a film thickness of 15
An 0 nm electrode was formed to obtain an organic EL device. This device has an emission luminance of 900 (cd / m ² ) at a DC voltage of 5V,
Maximum luminous brightness of 27300 (cd / m ² ), luminous efficiency 2.
A blue emission of 8 (lm / W) was obtained.

Example 45 Example 4 except that Alq3 is used as the electron injection layer.
An organic EL device was produced in the same manner as in 4. The device showed a light emission brightness of 490 cd / m ² at a direct current voltage 5V, maximum radiance 15800 (cd / m ^2), luminous efficiency 1.9
A blue emission of (lm / W) was obtained.

Example 46 In the same manner as in Example 44 except that an alloy obtained by mixing aluminum and lithium at a ratio of 30: 1 was used as the cathode electrode instead of the alloy obtained by mixing magnesium and silver at a ratio of 10: 1. An organic EL device was produced. This element has a DC voltage of 5
Luminous intensity at V of 950 cd / m ² , maximum luminous intensity of 290
A blue light emission of 00 (cd / m ² ) and a luminous efficiency of 3.0 (lm / W) was obtained.

Example 47 An organic EL device was manufactured in the same manner as in Example 4, except that a hole-injecting layer of metal-free phthalocyanine having a thickness of 5 nm was provided between the ITO electrode and the compound (42) by a vacuum evaporation method. Was produced. This device has a luminance of 900 at a DC voltage of 5V.
cd / m ² , maximum emission brightness 22200 (cd / m ² ),
Blue light emission with a luminous efficiency of 2.5 (lm / W) was obtained. Compared with the organic EL device of Example 44, the emission luminance is high when a low voltage is applied, which is advantageous for low voltage driving.

Comparative Example 1 Compound (42) was placed on a washed glass plate with an ITO electrode.
Was vacuum-deposited to form a hole injection layer having a film thickness of 50 nm. Then, Alq3 was vacuum-deposited to form a light emitting layer having a film thickness of 50 nm. On top of that, add magnesium and silver 10:
An electrode having a thickness of 100 nm was formed from the alloy mixed in Step 1 to obtain an organic EL device. Each thin film layer was vapor-deposited under a vacuum of 10 ⁻⁶ Torr and a substrate temperature of room temperature. This device has an emission luminance of 15 (cd / m ² ) at a DC voltage of 5 V, a maximum emission luminance of 12000 (cd / m ² ), and an emission efficiency of 1.1 (lm).
/ W).

Comparative Example 2 Compound (42) was applied onto a washed glass plate with an ITO electrode.
Was vacuum-deposited to form a hole injection layer having a film thickness of 50 nm. Then, 9,10-diphenylanthracene was vacuum-deposited to form a light emitting layer having a film thickness of 50 nm. in addition,
An alloy of magnesium and silver mixed at a ratio of 10: 1 with a film thickness of 10
An 0 nm electrode was formed to obtain an organic EL device. Each thin film layer was vapor-deposited under a vacuum of 10 ⁻⁶ Torr and a substrate temperature of room temperature. This device has a luminance of 2 at a DC voltage of 5V.
(Cd / m ² ), maximum emission brightness 2500 (cd / m ²
m ² ), and blue light emission with a luminous efficiency of 0.15 (lm / W) was obtained. However, there are many dark spots on the light emitting surface of this light emitting element, and the quality of the light emitting element is extremely poor.

Comparative Example 3 An organic EL device was prepared in the same manner as in Example 4, except that 9,10-diphenylanthracene was used as the light emitting material. This device has an emission luminance of 60 cd / m ² at a DC voltage of 5 V and a maximum emission luminance of 5800 (cd /
m ² ), and blue light emission with a luminous efficiency of 0.45 (lm / W) was obtained. As in Comparative Example 2, many dark spots were present on the light emitting surface of this light emitting device, and the quality as a light emitting device was extremely poor.

The organic EL device shown in this example provided light emission with a maximum emission luminance of 10,000 (cd / m ² ) or more, and all had high emission efficiency. When the organic EL device shown in this example was made to continuously emit light at 3 (mA / cm ² ), it was possible to observe a luminance of half or more of the initial luminance for 1000 hours or more. However, when the organic EL device of the comparative example was caused to emit light under the same conditions, it was attenuated to a luminance of half or less of the initial emission luminance in 500 hours or less. This is because the light emitting material represented by the general formula [1] and the general formula [2] of the present invention has extremely high fluorescence quantum efficiency, so that an element using this light emitting material can emit high-luminance light in a low current region. It has become possible to improve the life of the device. The organic EL device of the present invention achieves improvement of luminous efficiency, luminous brightness and prolongation of life, and is used together with a light emitting material, a doping material, a hole injection material, an electron injection material, a sensitizer,
The resin, the electrode material and the like and the method for manufacturing the element are not limited.

[0080]

The organic EL device using the organic EL device material of the present invention as a light emitting material exhibits blue light emission of high brightness and high luminous efficiency as compared with the conventional one, and an organic EL device having a long life can be obtained. It was

[Brief description of drawings]

FIG. 1 is an infrared absorption spectrum of compound (5).

FIG. 2 is an infrared absorption spectrum of the compound (6).

FIG. 3 is an infrared absorption spectrum of the compound (7).

Claims (6)

[Claims] 1. A light-emitting material for an organic electroluminescence device represented by the following general formula [1]. General formula [1] [In the formula, A to D are a substituted or unsubstituted alkyl group, a substituted or unsubstituted monocyclic group, a substituted or unsubstituted condensed polycyclic group, A and B or C and D are integrated into a nitrogen atom. Represents a heterocyclic group having a bond. ] 2. A light emitting material for an organic electroluminescence device, wherein A to D in the general formula [1] are substituted or unsubstituted monocyclic groups. 3. A light emitting material for organic electroluminescence device represented by the following general formula [2]. General formula [2] [Wherein, R ^{1 to} R ²³ are each independently a hydrogen atom, a halogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted amino group, a substituted or unsubstituted It represents a monocyclic group or a substituted or unsubstituted fused polycyclic group. Further, adjacent substituents may form a saturated or unsaturated ring. X ¹ ~
X ⁴ is each independently a direct bond, —O—, —S—,
_{> C = O,> SO 2} , - (CH 2) X -O- (CH 2)
_y − (where x and y are each independently 0 to 20
Represents a positive integer, but never x + y = 0. ), -P-,> P = O,> SiR ²¹ (R ²² ), NR
^{23 represents} a substituted or unsubstituted alkylene group or a substituted or unsubstituted aliphatic ring residue. ] 4. An organic electroluminescent device comprising a light emitting layer or a plurality of organic compound thin films including the light emitting layer formed between a pair of electrodes, wherein the light emitting layer comprises:
3. An organic electroluminescence device, which is a layer containing the light emitting material for an organic electroluminescence device according to any one of 3 above. 5. The organic electroluminescence device according to claim 4, wherein a layer containing an aromatic tertiary amine derivative and / or a phthalocyanine derivative is formed between the light emitting layer and the anode. 6. The organic electroluminescence device according to claim 4, wherein a layer containing a metal complex compound and / or a nitrogen-containing five-membered ring derivative is formed between the light emitting layer and the cathode.