WO2011065530A1

WO2011065530A1 - Organic luminous element

Info

Publication number: WO2011065530A1
Application number: PCT/JP2010/071254
Authority: WO
Inventors: 良明高橋
Original assignee: 昭和電工株式会社
Priority date: 2009-11-30
Filing date: 2010-11-29
Publication date: 2011-06-03
Also published as: JPWO2011065530A1; JP5706831B2

Abstract

Disclosed is an organic luminous element, in which an organic layer can be formed by coating and which has a long service life. Specifically disclosed is an organic luminous element which comprises a pair of electrodes and an organic compound layer composed of at least one layer and which can emit light upon the application of a voltage between the pair of electrodes. The organic luminous element is characterized in that at least one layer in the organic compound layer contains at least one ether compound represented by any one of formulae (1) to (3). (In formulae (1) to (3), A¹, A² and A³ independently represent a triarylamine derivative, a phenylcarbazole derivative containing at least two carbazole structures, a heteroaromatic compound derivative, a triarylborane derivative, or a tetraarylsilane derivative; and x, y and z independently represent an integer of 2 to 20.)

Description

Organic light emitting device

The present invention relates to an ether compound suitable as a material for an organic layer formed by coating in an organic light emitting device, and an organic light emitting device using the compound.

In recent years, materials having high luminous efficiency and durability have been actively developed in order to expand the applications of organic light emitting devices. However, in order to develop organic EL elements for displays and lighting applications, it is indispensable to develop materials that can maintain stable driving of the elements.

In addition, in order to reduce the manufacturing cost of organic light-emitting elements, technology development for forming an organic layer using a highly productive coating method has been carried out. Polymer materials have been developed (Patent Documents 1 and 2). However, the organic light emitting device manufactured using the coating method has a problem that the durability is lower than that of the organic light emitting device manufactured using the conventional vapor deposition method (Non-Patent Document 1).

JP 2008-169367 A JP 2007-84439 A

An object of the present invention is to provide an organic light-emitting element capable of forming an organic layer by coating and having a long lifetime.

As a result of intensive studies to solve the above problems, the present inventor has found that the lifetime of an organic light emitting device produced by coating film formation using an ether compound having a specific structure is extended, and the present invention has been completed. It came to do.

That is, the present invention relates to the following [1] to [8].

[1]
An organic light-emitting device comprising a pair of electrodes and one or more organic compound layers and emitting light by applying a voltage between the pair of electrodes, wherein at least one of the organic compound layers is represented by the following formulas (1) to (3): The organic light emitting element characterized by including any 1 or more types of the ether compound represented by these.

(In the above formulas (1) to (3), A ¹ , A ² and A ³ are each independently a triarylamine derivative group, a phenylcarbazole derivative group containing two or more carbazole structures, a heteroaromatic compound derivative group, tria Represents a reel borane derivative group or a tetraarylsilane derivative group, and x, y and z each independently represents an integer of 2 to 20.)
[2]
The organic light-emitting device according to the above [1], wherein at least one of the organic compound layers containing any one of the ether compounds represented by the formulas (1) to (3) is a light-emitting layer.

[3]
The organic light emitting device according to the above [2], wherein the light emitting layer contains a phosphorescent material.

[4]
In the above formula, any one of the above [1] to [3], wherein the oxygen atom adjacent to the methylene group is bonded to the carbon atom forming the aromatic ring in A ¹ , A ² or A ^3. Organic light emitting device.

[5]
Any one of the above [1] to [4], wherein at least one of the organic compound layers contains a compound represented by the formula (1), and in the formula (1), x represents an integer of 4 to 20. The organic light-emitting device described in 1.

[6]
The organic light-emitting device according to any one of [1] to [5], wherein A ¹ , A ^2, and A ³ in the formulas (1) to (3) have the same chemical structure.

[7]
The organic light-emitting device according to any one of the above [1] to [5], wherein A ¹ , A ² and A ³ in the formulas (1) to (3) have different chemical structures.

[8]
In the above formulas (1) to (3), A ¹ , A ² and A ³ are each independently selected from the following formulas (A-1) to (A-11): [1] to [7] (In the following formulas (A-1) to (A-11), a broken line represents a bond to an oxygen atom in the formulas (1) to (3)).

(In the formula (A-1), R ¹ , R ² and R ³ each independently has a substituent on a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group, a silyl group or an aromatic ring. Represents a diarylamino group which may have a substituent on the aromatic ring, n1 and n2 each independently represents an integer of 0 to 5, and n3 represents an integer of 0 to 4 , n1 is or different and each R ¹ identical if two or more, n2 is or different and each R ² is the same in the case of 2 or more, in the case of n3 is 2 or more R ³ may be the same or different.)

(In formula (A-2), R ⁴ , R ⁵ and R ⁶ are each independently a carbazolyl group optionally substituted with a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group, a silyl group or an alkyl group. Represents a carbazolylphenyl group which may be substituted with an alkyl group, a diarylamino group which may be substituted with an alkyl group or a diarylaminophenyl group which may be substituted with an alkyl group, and n4 represents 1 to 5 N5 represents an integer of 0 to 3, n6 represents an integer of 0 to 4, and when n4 is 2 or more, R ⁴ may be the same or different, and n5 is 2 or more. case or different and each R ⁵ is the same, in the case of n6 is 2 or more may be different in each of R ⁶ the same. provided that at least one of R ⁴ are also the carbazolyl group Wherein a carbazolylphenyl group.)

(In the formula (A-3), R ⁷ represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, n7 represents an integer of 1 to 4, and when n7 is 2 or more, R ⁷ may be the same or different, and Ar ¹ is substituted with an arene divalent group optionally substituted with an alkyl group, a carbazole divalent group optionally substituted with an alkyl group, or an alkyl group. Represents a divalent group of phenylcarbazole which may be present.)

(In the formula (A-4), Ar ² represents an aryl group which may be substituted with an alkyl group, a carbazolyl group which may be substituted with an alkyl group, or a carbazolylphenyl group which may be substituted with an alkyl group. N8 represents an integer of 1 to 4, and when n8 is 2 or more, Ar ^{2 s} may be the same or different.

(In the formula (A-5), Ar ³ may be a divalent group of an arene which may be substituted with an alkyl group, a divalent group of a carbazole which may be substituted with an alkyl group or an alkyl group. Represents a divalent group of phenylcarbazole, Ar ⁴ is an aryl group which may be substituted with an alkyl group, a carbazolyl group which may be substituted with an alkyl group, or a carbazolylphenyl which may be substituted with an alkyl group And n9 represents an integer of 1 to 3, and when n9 is 2 or more, Ar ⁴ may be the same or different.

(In the formula (A-6), Ar ⁵ may be a divalent group of an arene which may be substituted with an alkyl group, a divalent group of a carbazole which may be substituted with an alkyl group or an alkyl group. Represents a divalent group of phenylcarbazole, and Ar ⁶ represents an aryl group which may be substituted with an alkyl group, a carbazolyl group which may be substituted with an alkyl group, or a carbazolylphenyl which may be substituted with an alkyl group And n10 represents an integer of 1 to 2, and when n10 is 2, Ar ⁶ may be the same or different.

(In the formula (A-7), R ¹¹ and R ¹² each independently represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, and n11 and n12 each independently represents an integer of 1 to 5) the stands, n11 is or different and each is R ¹¹ identical if two or more, n12 is 2 or more when the R ¹² may .Ar ⁷ be different also in each identical divalent arene Represents a group.)

(In the formula (A-8), R ¹³ represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, n13 represents an integer of 0 to 5, and when n13 is 2 or more, R ¹³ may be the same or different.

(In the formula (A-9), R ¹⁴ represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, n14 represents an integer of 0 to 5, and when n14 is 2 or more, R ¹⁴ may be the same or different, and Ar ⁸ represents an arene divalent group.)

(In the formula (A-10), R ¹⁵ represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, n15 represents an integer of 0 to 5, and when n15 is 2 or more, R ¹⁵ may be the same or different, Ar ⁹ represents an arene divalent group, and Ar ¹⁰ represents an aryl group.

(In the formula (A-11), R ¹⁶ and R ¹⁷ each independently represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, and n16 and n17 each independently represents an integer of 0 to 4) R ¹⁶ may be the same or different when n16 is 2 or more, and R ¹⁷ may be the same or different when n17 is 2 or more Ar ¹¹ represents an aryl group .)

The organic light-emitting device of the present invention is excellent in life while being able to form an organic layer by a coating method.

Next, the present invention will be specifically described.

In the organic light-emitting device of the present invention, at least one of the organic compound layers contains any one of the ether compounds represented by the above formulas (1) to (3), and is formed by coating. The ether compounds represented by the formulas (1) to (3) are arylalkyl ether compounds, and in A ¹ to A ³ , the aryl group in the structure is bonded to the oxygen atom of the ether. These compounds are stable because the aryl group forms a strong bond with the oxygen atom, and the steric hindrance between A ¹ and A ³ is alleviated by a long ether linking group, thus extending the lifetime of the organic light emitting device. I think that. In addition, the above long ether linking group does not contain a chemically active functional group such as carbonyl, sulfone group, hydroxyl group or benzyl group, and has a high degree of structural freedom and suppresses crystallization in the film. Therefore, it is considered that the organic light emitting device has a longer life.

X in the above formula (1) represents an integer of 2 to 20. When x is 1, hydrolysis tends to occur, and when x exceeds 20, crystallinity increases and compatibility with other materials also decreases. Further, since steric hindrance between A ¹ and A ² can be further reduced, x is more preferably an integer of 4 to 20.

In the above formulas (2) and (3), x, y and z each independently represents an integer of 2 to 20. When x is 1, hydrolysis tends to occur, and when x exceeds 20, crystallinity increases and compatibility with other materials also decreases, so x, y, and z are 2 to 10 respectively. It is more preferable that it is an integer.

In the above formulas (1) to (3), A ¹ , A ² and A ³ are each independently a triarylamine derivative, a phenylcarbazole derivative containing two or more carbazole structures, a heteroaromatic compound derivative, a triarylborane derivative, Represents a tetraarylsilane derivative. More specifically, each of A ¹ , A ² and A ³ is preferably independently selected from chemical structures represented by the above formulas (A-1) to (A-11). These chemical structures have a hole transport property, an electron transport property, or an insulating property.

In the above formulas (A-1) to (A-11), R ¹ to R ⁷ and R ¹¹ to R ¹⁷ and R ¹⁸ to R ²⁷ described later are each independently a fluorine atom, a cyano group, an alkyl group, or an aryl group. Represents a substituent selected from an alkoxy group or a silyl group.

Examples of the alkyl group include methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, t-butyl group, amyl group, hexyl group, octyl group, decyl group and the like.

As the aryl group, for example, phenyl group, tolyl group, xylyl group, mesityl group, naphthyl group, biphenyl group, terphenyl group and pyridyl group, pyrazyl group, quinolyl group, isoquinolyl group, pyrrolyl group, imidazolyl group, pyrazolyl group, Examples include heteroaryl groups such as an oxazolyl group, an oxadiazolyl group, a toazolyl group, a benzoxazolyl group, a benzthiazolyl group, a thienyl group, a furyl group, a carbazolyl group, and a tetrazole group.
Examples of the alkoxy group include a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a butoxy group, an isobutoxy group, a t-butoxy group, a hexyloxy group, a 2-ethylhexyloxy group, and a decyloxy group.

Examples of the silyl group include a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, and a trimethoxysilyl group.

R ¹ to R ³ in the above formula (A-1) are further selected from a diarylaminophenyl group and a diarylamino group, and at least one of these groups is preferably selected. These diarylaminophenyl group and diarylamino group may have a substituent on the aromatic ring, and may be represented by the following formula (B-1) or (B-2), respectively.

(In the formula (B-1), R ¹⁸ , R ¹⁹ and R ²² each independently represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, and n18 and n19 each independently represents 0. And n22 represents an integer of 0 to 4, and when two or more substituents are present on the same aromatic ring, they may be the same or different.

(In the formula (B-2), R ²⁶ and R ²⁷ are each independently a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group, a silyl group, or a diarylamino group (specific examples of an aryl group in a diarylamino group). And n26 and n27 each independently represents an integer of 0 to 5, and when two or more substituents are present on the same aromatic ring, they are the same or different. May be.)
R ⁴ to R ⁶ in the above formula (A-2) are further selected from a carbazolyl group, a carbazolylphenyl group, a diarylamino group and a diarylaminophenyl group, and these groups are alkyl groups (specific examples of alkyl groups are The same as above, and may be substituted. At least one of R ⁴ is the carbazolyl group or the carbazolylphenyl group. When only one carbazole structure is included in the structure represented by the formula (A-2), the durability of the organic light emitting device is not greatly improved.

Ar ¹ , Ar ³ and Ar ⁵ in the above formulas (A-3) to (A-6) are each independently an arene optionally substituted with an alkyl group (for example, benzene, toluene, xylene, mesitylene, naphthalene, biphenyl) , Terphenyl) is substituted with a divalent group (a group in which two hydrogen atoms on the aromatic ring of an arene are removed. That is, an arylene group), an alkyl group (specific examples of the alkyl group are the same as those described above). The divalent group of phenylcarbazole which may be substituted with a divalent group of carbazole which may be substituted (a group obtained by removing two hydrogen atoms of carbazole) or an alkyl group (specific examples of the alkyl group are the same as those described above). Represents a group (a group in which two hydrogen atoms of phenylcarbazole have been removed). Ar ² , Ar ⁴ and Ar ⁶ are each independently an aryl group (eg, phenyl group, tolyl group) optionally substituted with a hydrogen atom or an alkyl group (specific examples of the alkyl group are the same as those described above). , A xylyl group, a mesityl group, a naphthyl group, a biphenyl group, a terphenyl group), an alkyl group (specific examples of the alkyl group are the same as those described above), and a carbazolyl group or an alkyl group (of the alkyl group). Specific examples are the same as above.) Represents a carbazolylphenyl group which may be substituted.

Ar ⁷ to Ar ¹¹ in the above formulas (A-7) and (A-9) to (A-11) are each independently 2 of arene (eg, benzene, toluene, xylene, mesitylene, naphthalene, biphenyl, terphenyl). A valent group (a group in which two hydrogen atoms on the aromatic ring of an arene are removed, that is, an arylene group) is represented.

Examples of the triarylamine derivative group represented by the above formula (A-1) include groups represented by the following general formula (A-12) or (A-13).

(In the formula (A-12), R ¹⁷ to R ²² each independently represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, and n17 to n19 each independently represents an integer of 0 to 5) N20 to n22 each independently represents an integer of 0 to 4, and when two or more substituents are present on the same aromatic ring, they may be the same or different.

(In the formula (A-13), R ²³ to R ²⁵ each independently represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, R ²⁶ and R ²⁷ each independently represent a fluorine atom, Represents a cyano group, an alkyl group, an aryl group, an alkoxy group, a silyl group or a diarylamino group (specific examples of the aryl group in the diarylamino group are the same as those described above), and n23, n26 and n27 each independently represents 0 to And n24 and n25 each independently represents an integer of 0 to 4, and when having two or more substituents on the same aromatic ring, they may be the same or different.
Specific preferred examples of the above formulas A ^1, A ² and A ³ in the following, the present invention is not limited thereto.

An example of the configuration of the organic light emitting device according to the present invention includes a configuration in which a hole transport layer, a light emitting layer, and an electron transport layer are laminated in this order between an anode and a cathode provided on a transparent substrate. In the configuration of another organic light emitting device, for example, either 1) a hole transport layer / light emitting layer or 2) a light emitting layer / electron transport layer may be provided between the anode and the cathode of the organic light emitting device. 3) a layer containing a hole transport material, a light emitting material, an electron transport material, 4) a layer containing a hole transport material, a light emitting material, 5) a layer containing a light emitting material, an electron transport material, 6) Any one of the layers may be provided. Further, two or more light emitting layers may be stacked. The organic layer may be formed inside pores (cavities) provided in the electrode surface on the substrate.

The ether compounds represented by the above formulas (1) to (3) may be contained in any of the hole transport layer, the light emitting layer, and the electron transport layer, but extend the life of the organic light emitting device. From the viewpoint of high effect, it is particularly preferably contained in the light emitting layer. When included in the hole transport layer and the electron transport layer, the layer is composed of a single compound represented by the above formulas (1) to (3), or is formed with a small amount of an oxidizing dopant or a reducing dopant. It is preferable to include 90% by weight or more of the compounds represented by the above formulas (1) to (3). Further, when contained in the light emitting layer, the compounds represented by the above formulas (1) to (3) are preferably contained in the light emitting layer at a concentration of 25 to 98% by weight, and the light emitting material forming the light emitting layer It is more preferable that all materials other than those are compounds represented by the above formulas (1) to (3).

As the substrate of the organic light emitting device of the present invention, an insulating substrate transparent to the emission wavelength of the light emitting material is preferably used. Specifically, in addition to glass, transparent materials such as PET (polyethylene terephthalate) and polycarbonate are used. Plastic or the like is used.

Each organic compound layer may be formed by mixing a polymer material as a binder. Examples of the polymer material include polymethyl methacrylate, polycarbonate, polyester, polysulfone, and polyphenylene oxide.

The materials used for the above layers may be formed by mixing materials having different functions, for example, light emitting materials, hole transport materials, electron transport materials, and the like. The organic compound layer containing the phosphorescent polymer compound may also contain other hole transport materials and / or electron transport materials for the purpose of supplementing charge transport properties.

The light-emitting layer preferably contains a phosphorescent compound. Examples of the phosphorescent compound include iridium complexes having a ligand such as arylpyridine and carbene, platinum complexes, and osmium complexes. More specific examples of the iridium complex include the following compounds (E1-1) to (E1-39).

A hole injection layer may be provided between the anode and the light emitting layer in order to relax the injection barrier in hole injection. In order to form the hole injection layer, a known material such as copper phthalocyanine, a mixture of polyethylene dioxythiophene (PEDOT) and polystyrene sulfonic acid (PSS), fluorocarbon, silicon dioxide or the like is used.

An insulating layer having a thickness of 0.1 to 10 nm is provided between the cathode and the electron transport layer or between the cathode and the organic compound layer laminated adjacent to the cathode in order to improve the electron injection efficiency. It may be. In order to form the insulating layer, known materials such as lithium fluoride, sodium fluoride, magnesium fluoride, magnesium oxide, and alumina are used.

As the hole transport material forming the hole transport layer or the hole transport material mixed in the light emitting layer, for example, TPD (N, N′-dimethyl-N, N ′-(3-methylphenyl)- Α-NPD (4,4′-bis [N- (1-naphthyl) -N-phenylamino] biphenyl); m-MTDATA (4,4 ′, 1,1′-biphenyl-4,4′diamine); Low molecular weight triphenylamine derivatives such as 4 ″ -tris (3-methylphenylphenylamino) triphenylamine), low molecular weight such as 4,4′-dicarbazolylbiphenyl, 1,3-dicarbazolylbiphenyl And carbazole derivatives. The above hole transport materials may be used singly or in combination of two or more, or different hole transport materials may be laminated and used. The thickness of the hole transport layer depends on the electrical conductivity of the hole transport layer and cannot be generally limited, but is preferably 1 nm to 5 μm, more preferably 5 nm to 1 μm, and particularly preferably 10 nm to 500 nm. Is desirable.

Examples of the electron transport material for forming the electron transport layer or the electron transport material mixed in the light emitting layer include quinolinol derivative metal complexes such as Alq3 (aluminum triskinolinolate), oxadiazole derivatives, triazole derivatives, imidazole. Examples include known compounds such as derivatives, triazine derivatives, and triarylborane derivatives. The electron transport materials may be used singly or in combination of two or more, or different electron transport materials may be laminated and used. The thickness of the electron transport layer depends on the electrical conductivity of the electron transport layer and cannot be generally limited, but is preferably 1 nm to 5 μm, more preferably 5 nm to 1 μm, and particularly preferably 10 nm to 500 nm. .

In addition, a hole blocking layer is provided adjacent to the cathode side of the light emitting layer for the purpose of preventing holes from passing through the light emitting layer and efficiently recombining holes and electrons in the light emitting layer. May be. In order to form the hole blocking layer, a known material such as a triazole derivative, an oxadiazole derivative, or a phenanthroline derivative is used.

Examples of film formation methods for the light-emitting layer, the hole transport layer, and the electron transport layer include dry coating methods such as resistance heating evaporation, electron beam evaporation, and sputtering, as well as spin coating, casting, and microgravure. Wet film forming methods such as coating methods, gravure coating methods, bar coating methods, roll coating methods, wire bar coating methods, dip coating methods, spray coating methods, screen printing methods, flexographic printing methods, offset printing methods, and inkjet printing methods ( Application method) can be used. The layer containing the compound of the present invention has an advantage that it can be formed by a coating method capable of suppressing the manufacturing cost of the organic light emitting device.

As an anode material used for the organic light emitting device of the present invention, for example, a known transparent conductive material such as ITO (indium tin oxide), tin oxide, zinc oxide, polythiophene, polypyrrole, polyaniline or the like is preferably used. It is done. The surface resistance of the electrode formed of this transparent conductive material is preferably 1 to 50Ω / □ (ohm / square). The thickness of the anode is preferably 50 to 300 nm.

Examples of the cathode material used in the organic EL device of the present invention include alkali metals such as Li, Na, K, and Cs; alkaline earth metals such as Mg, Ca, and Ba; Al; MgAg alloys; Al such as AlLi and AlCa A known cathode material such as an alloy of alkali metal or alkaline earth metal is preferably used. The thickness of the cathode is preferably 10 nm to 1 μm, more preferably 50 to 500 nm. When a highly active metal such as an alkali metal or alkaline earth metal is used, the thickness of the cathode is preferably 0.1 to 100 nm, more preferably 0.5 to 50 nm. In this case, a metal layer that is stable to the atmosphere is laminated on the cathode for the purpose of protecting the cathode metal. Examples of the metal forming the metal layer include Al, Ag, Au, Pt, Cu, Ni, and Cr. The thickness of the metal layer is preferably 10 nm to 1 μm, more preferably 50 to 500 nm.

In addition, as a method for forming the anode material, for example, an electron beam evaporation method, a sputtering method, a chemical reaction method, a coating method, or the like is used. As a method for forming the cathode material, for example, a resistance heating evaporation method, An electron beam evaporation method, a sputtering method, an ion plating method, or the like is used.

The organic light-emitting device of the present invention is suitably used in an image display device as a matrix or segment pixel by a known method. The organic EL element is also suitably used as a surface light source without forming pixels.

Specifically, the organic light-emitting device of the present invention is suitably used for displays, backlights, electrophotography, illumination light sources, recording light sources, exposure light sources, reading light sources, signs, signboards, interiors, optical communications, and the like.

Next, the present invention will be described in more detail with reference to examples, but the present invention is not limited thereto.

Synthesis Example 1 Synthesis of Compound (A1) Compound (A1) was synthesized as shown in the following scheme.

That is, 1.665 g (3.45 mmol) of tri (4-bromophenyl) amine, 1.90 g (6.57 mmol) of N- (3-benzyloxyphenyl) -m-toluidine, N- (3-methylphenyl) aniline 0.63 g (3.44 mmol), palladium acetate 45 mg (0.20 mmol), tri-t-butylphosphine 130 mg (0.64 mmol) and potassium tert-butoxide 1.39 g (12.4 mmol) are dissolved in 50 ml of toluene. And heated to reflux for 3 hours. The resulting reaction mixture was filtered through celite, and then the filtrate was concentrated under reduced pressure and purified by silica gel column chromatography (eluent: hexane / toluene = 1/1 volume ratio). To this was added 100 mg of palladium black, 2.0 g (40 mmol) of hydrazine monohydrate, 20 ml of toluene and 40 ml of ethanol, and the mixture was heated to reflux for 2 hours. The obtained reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure and purified by silica gel column chromatography (eluent: toluene). This crude product was dissolved in a small amount of toluene, and hexane was added little by little to recrystallize to obtain 0.70 g (0.87 mmol) of a synthetic intermediate (B1).

Next, 0.50 g (0.62 mmol) of intermediate (B1) and 67 mg (0.31 mmol) of 1,4-dibromobutane were dissolved in 5 ml of N, N-dimethylformamide, and 30 mg (0.75 mmol) of sodium hydride was dissolved. In addition, the mixture was stirred at room temperature for 24 hours. Water was added to the resulting reaction solution, and the resulting precipitate was collected by filtration, dried under reduced pressure, and purified by silica gel column chromatography (eluent: toluene). This crude product was dissolved in a small amount of toluene, and hexane was added little by little to recrystallize to obtain 0.45 g (0.27 mmol) of the synthetic compound (A1).

The identification data of the compound (A1) is as follows.

Calcd _{_{_{(C 118 H 102 N 8 O}}} 2) C, 85.17; H, 6.18; N, 6.73. : Measured value C, 85.49; H, 6.22; N, 6.51.
Mass spectrometry (FAB +): 1664 (M ⁺ ).
Synthesis Example 2 Synthesis of Compound (A2) Compound (A2) was synthesized as shown in the following scheme.

That is, 3.0 g (17 mmol) of 3-bromophenol and 1.72 g (8.5 mmol) of 1,3-dibromopropane were dissolved in 20 ml of N, N-dimethylformamide, and 700 mg (17.5 mmol) of sodium hydride was dissolved. In addition, the mixture was stirred at room temperature for 24 hours. Water was added to the resulting reaction solution, and the mixture was extracted with hexane, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane / chloroform = 1/1 volume ratio) to obtain 3.2 g (8.3 mmol) of a synthetic intermediate (B2).

Next, 2.5 g (6.5 mmol) of intermediate (B2), 1.38 g (6.5 mmol) of o-tolidine, 3.33 g (19.5 mmol) of 3-bromotoluene, 100 mg (0.45 mmol) of palladium acetate, 300 mg (1.48 mmol) of tri-t-butylphosphine and 4.0 g (36 mmol) of potassium-t-butoxide were dissolved in 50 ml of toluene and heated to reflux for 3 hours. The resulting reaction mixture was filtered through celite, the filtrate was concentrated under reduced pressure, and purified by silica gel column chromatography (eluent: hexane / toluene = 2/3 volume ratio). The obtained crude product was dissolved in a small amount of toluene, and hexane was added little by little to recrystallize to obtain 0.40 g (0.34 mmol) of compound (A2).

The identification data of the compound (A2) is as follows.

Calcd _{_{_{(C 85 H 80 N 4 O}}} 2) C, 85.82; H, 6.78; N, 4.71. : Measured value C, 85.46; H, 6.59; N, 4.63.
Mass spectrometry (FAB +): 1189 (M ⁺ ).
Synthesis Example 3 Synthesis of Compound (A3) Compound (A3) was synthesized as shown in the following scheme.

A synthesis intermediate using 2.0 g (5.85 mmol) of 1-benzyloxy-3,5-dibromophenol and 2.3 g (11.7 mmol) of di-m-tolylamine in the same manner as the synthesis of the compound (B1). (B3) was synthesized.

Next, a mixture of 3.0 g (9.5 mmol) of 2,4,6-tribromopyridine, 2.3 g (19 mmol) of phenylboronic acid and 0.10 g (0.087 mmol) of tetrakis (triphenylphosphine) palladium 2-Dimethoxyethane (50 ml) and potassium carbonate aqueous solution (50 ml) were added, and the mixture was heated to reflux for 2 hours. Thereafter, 2.2 g (9.6 mmol) of 3-benzyloxyphenylboronic acid was added, and the mixture was further heated to reflux for 2 hours. The organic layer was extracted from the obtained reaction solution, and the solvent was distilled off under reduced pressure. To the residue, 100 mg of palladium black, 2.0 g (40 mmol) of hydrazine monohydrate, 20 ml of toluene and 40 ml of ethanol were added and heated under reflux for 2 hours. The obtained reaction mixture was purified by silica gel column chromatography to obtain 2.0 g (6.2 mmol) of a synthetic intermediate (B4).

Next, 1.0 g (2.1 mmol) of compound (B3), 0.67 g (2.1 mmol) of (B4) and 0.72 g (2.0 mmol) of (B5) were dissolved in 15 ml of N, N-dimethylformamide, Sodium hydride 0.20 g (8.3 mmol) was added, and the mixture was stirred at room temperature for 24 hours. Water was added to the resulting reaction solution, and the resulting precipitate was collected by filtration, dried under reduced pressure, and purified by silica gel column chromatography to obtain 0.40 g (0.40 mmol) of compound (A3).

Synthesis Example 4 Synthesis of Compound (A4) Compound (A4) was synthesized as shown in the following scheme.

Using carbazole 2.0 g (12 mmol), 4-benzyloxycarbazole 3.3 g (12 mmol) and 4,4′-dibromo-2,2′-dimethylbiphenyl in the same manner as in the synthesis of compound (B1), Body (B6) was synthesized.

Next, 1.0 g (1.9 mmol) of the synthetic intermediate (B6) and 0.30 g (0.61 mmol) of the compound (B7) were dissolved in 10 ml of N, N-dimethylformamide, and 0.20 g of sodium hydride (8 .3 mmol) was added and stirred at room temperature for 24 hours. Water was added to the resulting reaction solution, and the resulting precipitate was collected by filtration, dried under reduced pressure, and purified by silica gel column chromatography to obtain 1.0 g (0.54 mmol) of compound (A4).

Synthesis Example 5 Synthesis of Compound (A5) Compound (A5) was synthesized as shown in the following scheme.

To a mixture of 2.0 g (11 mmol) of cyanuric chloride, 3.9 g (22 mmol) of 4-tert-butylphenylboronic acid and 0.10 g (0.087 mmol) of tetrakis (triphenylphosphine) palladium, 50 ml of 1,2-dimethoxyethane and 50 ml of an aqueous potassium carbonate solution was added and the mixture was heated to reflux for 2 hours. Thereafter, 2.5 g (11 mmol) of 3-benzyloxyphenylboronic acid was added, and the mixture was further heated to reflux for 2 hours. The organic layer was extracted from the obtained reaction solution, and the solvent was distilled off under reduced pressure. To the residue, 100 mg of palladium black, 2.0 g (40 mmol) of hydrazine monohydrate, 20 ml of toluene and 40 ml of ethanol were added and heated under reflux for 2 hours. The obtained reaction mixture was purified by silica gel column chromatography to obtain 1.0 g (2.3 mmol) of a synthetic intermediate (B8).

Next, the obtained synthetic intermediate (B8) and 0.31 g (1.1 mmol) of 1,8-dibromooctane were dissolved in 10 ml of N, N-dimethylformamide, and 0.20 g (8.3 mmol) of sodium hydride was dissolved. And stirred at room temperature for 24 hours. Water was added to the resulting reaction solution, and the resulting precipitate was collected by filtration, dried under reduced pressure, and purified by silica gel column chromatography to obtain 1.0 g (1.0 mmol) of compound (A5).

Synthesis Example 6 Synthesis of Compound (A6) Compound (A6) was synthesized as shown in the following scheme.

Compound (B9) (2.0 g, 3.2 mmol), 3-benzyloxyphenylboronic acid (1.0 g, 4.4 mmol) and tetrakis (triphenylphosphine) synthesized by a method similar to the method described in WO2005-61562 To a mixture of 0.10 g (0.087 mmol) of palladium, 25 ml of 1,2-dimethoxyethane and 30 ml of aqueous potassium carbonate solution were added, and the mixture was heated to reflux for 2 hours. The organic layer was extracted from the obtained reaction solution, and the solvent was distilled off under reduced pressure. To the residue, 100 mg of palladium black, 2.0 g (40 mmol) of hydrazine monohydrate, 20 ml of toluene and 40 ml of ethanol were added and heated under reflux for 2 hours. The obtained reaction mixture was purified by silica gel column chromatography to obtain 1.4 g (2.5 mmol) of a synthetic intermediate (B10).

Next, 1.0 g (1.8 mmol) of the obtained synthetic intermediate (B10) was used, and 1,3-dibromobenzene was used instead of 4,4′-dibromo-2,2′-dimethylbiphenyl. The compound (B11) 0.76 g (1.8 mmol) and 1,10-dibromodecane 0.24 g (0.9 mmol) synthesized in the same manner as in (1) were dissolved in 10 ml of N, N-dimethylformamide and hydrogenated. Sodium 0.20 g (8.3 mmol) was added and stirred at room temperature for 24 hours. Water was added to the resulting reaction solution, and the resulting precipitate was collected by filtration, dried under reduced pressure, and purified by silica gel column chromatography to obtain 0.20 g (0.18 mmol) of compound (A6).

Synthesis Example 7 Synthesis of Compound (A7) Compound (A7) was synthesized as shown in the following scheme.

Compound (B12) (2.0 g, 5.6 mmol), 3-benzyloxyphenylboronic acid (1.3 g, 5.7 mmol) and tetrakis (triphenyl) synthesized in the same manner as described in JP-A-2008-227382 To a mixture of phosphine) palladium (0.10 g, 0.087 mmol), 25 ml of 1,2-dimethoxyethane and 30 ml of an aqueous potassium carbonate solution were added and heated to reflux for 2 hours. The organic layer was extracted from the obtained reaction solution, and the solvent was distilled off under reduced pressure. To the residue, 100 mg of palladium black, 2.0 g (40 mmol) of hydrazine monohydrate, 20 ml of toluene and 40 ml of ethanol were added and heated under reflux for 2 hours. The obtained reaction mixture was purified by silica gel column chromatography to obtain 1.8 g (4.9 mmol) of a synthetic intermediate (B13).

Next, 2.0 g (11 mmol) of N-phenyl-o-phenylenediamine and 3.2 g (11 mmol) of N- (3-benzyloxyphenyl) -o-phenylenediamine were dissolved in 20 ml of 1,2-dichloroethane, 1.2 g (5.9 mmol) of terephthaloyl and 20 ml of phosphoryl chloride were added and heated to reflux for 8 hours. The reaction solution was added to 100 ml of water, the organic layer was extracted, and the solvent was distilled off under reduced pressure. The residue was purified by liquid gel column chromatography to obtain 0.70 g (1.5 mmol) of a synthetic intermediate (B14).

Next, 0.55 g (1.5 mmol) of compound (B13), 0.70 g (1.5 mmol) of (B14) and 0.16 g (0.74 mmol) of 1,4-dibromobutane were added to 5 ml of N, N-dimethylformamide. After dissolution, 0.10 g (4.2 mmol) of sodium hydride was added and stirred at room temperature for 24 hours. Water was added to the resulting reaction solution, and the resulting precipitate was collected by filtration, dried under reduced pressure, and purified by silica gel column chromatography to obtain 0.20 g (0.22 mmol) of compound (A7).

Example 1
A substrate with ITO (manufactured by Nippon Electric Co., Ltd.) was used. This was a substrate in which two ITO (indium tin oxide) electrodes (anodes) having a width of 4 mm were formed in one stripe on one surface of a 25 mm square glass substrate.

First, N, N′-di (1-naphthyl) -N, N′-diphenyl-4,4′-diaminobiphenyl (manufactured by Sigma-Aldrich, sublimation purified product, purity 99%) on the above-mentioned ITO-coated substrate. A hole transport layer was formed to a thickness of about 50 nm at a rate of 0.2 nm / sec by resistance heating vapor deposition under a reduced pressure of 8.5 × 10 ⁻⁵ Pa. Next, 10 mg of the phosphorescent emitter (E1-20) (that is, the above compound E1-20), 45 mg of the compound (A1) and 45 mg of the following compound (C-1) were added to toluene (Wako Pure Chemical Industries, Ltd.). The solution was dissolved in 2900 mg and filtered through a filter having a pore size of 0.2 μm to prepare a coating solution. Next, the coating solution was coated on the hole transport layer by a spin coating method under the conditions of a rotation speed of 3000 rpm and a coating time of 30 seconds. After the application, it was dried at room temperature (25 ° C.) for 30 minutes to form a light emitting layer. The film thickness of the obtained light emitting layer was about 50 nm.

Next, 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (manufactured by Sigma-Aldrich, sublimation purified product, purity 99.99%) and Alq3 (manufactured by Tokyo Chemical Industry Co., Ltd.) are formed on the light emitting layer. , Sublimation refined product, purity 98%) under reduced pressure of 8.5 × 10 ⁻⁵ Pa by resistance heating vapor deposition method to a film thickness of 20 nm and 30 nm respectively at a rate of 0.2 nm / sec. An electron transport layer was formed. Next, barium and aluminum were co-evaporated at a weight ratio of 1:10 under a reduced pressure of 8.5 × 10 ⁻⁵ Pa, and a cathode having a width of 3 mm was striped in a stripe shape so as to be orthogonal to the extending direction of the anode. The book was formed. The film thickness of the obtained cathode was about 50 nm.

Finally, in an argon atmosphere, lead wires (wirings) were attached to the anode and the cathode to produce four organic light emitting elements of 4 mm length × 3 mm width. When the organic EL element was made to emit light by applying a voltage using a programmable DC voltage / current source (TR6143, manufactured by Advantest Co., Ltd.), the lifetime of the organic light emitting element (initial luminance 200 cd / m2 in constant current driving) was obtained. The luminance half time of was 7500 hours.

(Comparative Example 1)
An organic light emitting device was produced in the same manner as in Example 1 except that 45 mg of the following compound (C-2) was used instead of 45 mg of the compound (A1). The lifetime of the organic light emitting device was 2400 hours. It was.

(Comparative Example 2)
An organic light-emitting device was prepared in the same manner as in Example 1 except that 45 mg of the following compound (C-3) was used instead of 45 mg of the compound (A1), and a voltage was applied within 1 hour. Short-circuited and stopped emitting light.

(Example 2)
Instead of 10 mg phosphorescent emitter (E1-20), 45 mg compound (A1) and 45 mg compound (C-1), 10 mg phosphorescent emitter (E1-6) (ie, the above compound E1-6), An organic light emitting device was produced in the same manner as in Example 1 except that 45 mg of the compound (A2) and 45 mg of the following compound (C-4) were used. The lifetime of the organic light emitting device was 4900 hours.

(Comparative Example 3)
An organic light emitting device was produced in the same manner as in Example 2 except that 45 mg of the following compound (C-5) was used instead of 45 mg of the compound (A2). The lifetime of the organic light emitting device was 1900 hours. It was.

(Comparative Example 4)
An organic light emitting device was produced in the same manner as in Example 2 except that 90 mg of the following compound (C-6) was used instead of 45 mg of the compound (A2) and 45 mg of the compound (C-4). The lifetime of the light emitting element was 800 hours.

(Example 3)
Instead of 10 mg phosphorescent emitter (E1-20), 45 mg compound (A1) and 45 mg compound (C-1), 10 mg phosphorescent emitter (E1-2) (ie compound E1-2 above) and An organic light emitting device was produced in the same manner as in Example 1 except that 90 mg of the compound (A3) was used. The lifetime of the organic light emitting device was 8000 hours.

Example 4
Instead of 10 mg phosphorescent emitter (E1-20), 45 mg compound (A1) and 45 mg compound (C-1), 10 mg phosphorescent emitter (E1-38) (ie, compound E1-38 above), An organic light emitting device was produced in the same manner as in Example 1 except that 45 mg of the compound (A4) and 45 mg of the compound (A5) were used. The lifetime of the organic light emitting device was 5000 hours.

(Example 5)
Instead of 10 mg phosphorescent emitter (E1-20), 45 mg compound (A1) and 45 mg compound (C-1), 10 mg phosphorescent emitter (E1-24) (ie compound E1-24 above) and An organic light emitting device was produced in the same manner as in Example 1 except that 90 mg of the compound (A6) was used, and the lifetime of the organic light emitting device was 8500 hours.

(Example 6)
Instead of 10 mg of phosphorescent emitter (E1-20), 45 mg of compound (A1) and 45 mg of compound (C-1), 4 mg of phosphorescent emitter (E1-32) (ie, the above compound E1-32), An organic light emitting device was produced in the same manner as in Example 1 except that 48 mg of the compound (A1) and 48 mg of the compound (A7) were used. The lifetime of the organic light emitting device was 9400 hours.

As is apparent from Table 1, the organic light-emitting device produced using the compound of the present invention has a longer lifetime than the organic light-emitting device produced using conventional polymer materials and low molecular compounds.

Claims

An organic light-emitting device comprising a pair of electrodes and one or more organic compound layers and emitting light by applying a voltage between the pair of electrodes, wherein at least one of the organic compound layers is represented by the following formulas (1) to (3): The organic light emitting element characterized by including any 1 or more types of the ether compound represented by these.

(In the above formulas (1) to (3), A 1 , A 2 and A 3 are each independently a triarylamine derivative group, a phenylcarbazole derivative group containing two or more carbazole structures, a heteroaromatic compound derivative group, tria Represents a reel borane derivative group or a tetraarylsilane derivative group, and x, y and z each independently represents an integer of 2 to 20.)
2. The organic light-emitting device according to claim 1, wherein at least one of the organic compound layers containing any one of the ether compounds represented by the formulas (1) to (3) is a light-emitting layer.
The organic light emitting device according to claim 2, wherein the light emitting layer contains a phosphorescent light emitter.
The organic light-emitting device according to any one of claims 1 to 3, wherein an oxygen atom adjacent to the methylene group in the above formula is bonded to a carbon atom forming an aromatic ring in A 1 , A 2 or A 3. element.
The organic compound layer according to any one of claims 1 to 4, wherein at least one layer of the organic compound layer includes a compound represented by the formula (1), and in the formula (1), x represents an integer of 4 to 20. Organic light emitting device.
6. The organic light emitting device according to claim 1 , wherein A 1 , A 2 and A 3 in the formulas (1) to (3) have the same chemical structure.
6. The organic light-emitting device according to claim 1 , wherein A 1 , A 2 and A 3 in the formulas (1) to (3) have different chemical structures.
8. The method according to claim 1, wherein A 1 , A 2 and A 3 in the formulas (1) to (3) are each independently selected from the following formulas (A-1) to (A-11): One of the organic light-emitting devices according to one of the following formulas (in the following formulas (A-1) to (A-11), a broken line represents a bond to an oxygen atom in the formulas (1) to (3)).

(In the formula (A-1), R 1 , R 2 and R 3 each independently has a substituent on a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group, a silyl group or an aromatic ring. Represents a diarylamino group which may have a substituent on the aromatic ring, n1 and n2 each independently represents an integer of 0 to 5, and n3 represents an integer of 0 to 4 , n1 is or different and each R 1 identical if two or more, n2 is or different and each R 2 is the same in the case of 2 or more, in the case of n3 is 2 or more R 3 may be the same or different.)

(In formula (A-2), R 4 , R 5 and R 6 are each independently a carbazolyl group optionally substituted with a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group, a silyl group or an alkyl group. Represents a carbazolylphenyl group which may be substituted with an alkyl group, a diarylamino group which may be substituted with an alkyl group or a diarylaminophenyl group which may be substituted with an alkyl group, and n4 represents 1 to 5 N5 represents an integer of 0 to 3, n6 represents an integer of 0 to 4, and when n4 is 2 or more, R 4 may be the same or different, and n5 is 2 or more. case or different and each R 5 is the same, in the case of n6 is 2 or more may be different in each of R 6 the same. provided that at least one of R 4 are also the carbazolyl group Wherein a carbazolylphenyl group.)

(In the formula (A-3), R 7 represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, n7 represents an integer of 1 to 4, and when n7 is 2 or more, R 7 may be the same as or different from each other, Ar 1 is substituted with a divalent group of an arene which may be substituted with an alkyl group, a divalent group of a carbazole which may be substituted with an alkyl group or an alkyl group. Represents a divalent group of phenylcarbazole which may be present.)

(In the formula (A-4), Ar 2 represents an aryl group which may be substituted with an alkyl group, a carbazolyl group which may be substituted with an alkyl group, or a carbazolylphenyl group which may be substituted with an alkyl group. N8 represents an integer of 1 to 4, and when n8 is 2 or more, Ar 2 s may be the same or different.

(In the formula (A-5), Ar 3 may be a divalent group of an arene which may be substituted with an alkyl group, a divalent group of a carbazole which may be substituted with an alkyl group or an alkyl group. Represents a divalent group of phenylcarbazole, Ar 4 is an aryl group optionally substituted with an alkyl group, a carbazolyl group optionally substituted with an alkyl group, or a carbazolylphenyl optionally substituted with an alkyl group And n9 represents an integer of 1 to 3, and when n9 is 2 or more, Ar 4 may be the same or different.

(In the formula (A-6), Ar 5 may be a divalent group of an arene which may be substituted with an alkyl group, a divalent group of a carbazole which may be substituted with an alkyl group or an alkyl group. Represents a divalent group of phenylcarbazole, and Ar 6 represents an aryl group which may be substituted with an alkyl group, a carbazolyl group which may be substituted with an alkyl group, or a carbazolylphenyl which may be substituted with an alkyl group And n10 represents an integer of 1 to 2, and when n10 is 2, Ar 6 may be the same or different.

(In the formula (A-7), R 11 and R 12 each independently represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, and n11 and n12 each independently represents an integer of 1 to 5) the stands, n11 is or different and each is R 11 identical if two or more, n12 is 2 or more when the R 12 may .Ar 7 be different also in each identical divalent arene Represents a group.)

(In the formula (A-8), R 13 represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, n13 represents an integer of 0 to 5, and when n13 is 2 or more, R 13 may be the same or different.

(In the formula (A-9), R 14 represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, n14 represents an integer of 0 to 5, and when n14 is 2 or more, R 14 may be the same or different, and Ar 8 represents an arene divalent group.)

(In the formula (A-10), R 15 represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, n15 represents an integer of 0 to 5, and when n15 is 2 or more, R 15 may be the same or different, Ar 9 represents an arene divalent group, and Ar 10 represents an aryl group.

(In the formula (A-11), R 16 and R 17 each independently represents a fluorine atom, a cyano group, an alkyl group, an aryl group, an alkoxy group or a silyl group, and n16 and n17 each independently represents an integer of 0 to 4) R 16 may be the same or different when n16 is 2 or more, and R 17 may be the same or different when n17 is 2 or more Ar 11 represents an aryl group .)