JP6360796B2 - Material for organic electroluminescence device and organic electroluminescence device using the same - Google Patents

Description

  The present invention relates to an organic electroluminescent element containing a carborane compound, and more particularly to a thin film device that emits light by applying an electric field to a light emitting layer made of an organic compound.

  In general, an organic electroluminescence element (hereinafter referred to as an organic EL element) has a light emitting layer and a pair of counter electrodes sandwiching the layer as its simplest structure. That is, in an organic EL element, when an electric field is applied between both electrodes, electrons are injected from the cathode, holes are injected from the anode, and these are recombined in the light emitting layer to emit light. .

In recent years, an organic EL element using an organic thin film has been developed. In particular, in order to increase luminous efficiency, the type of electrode was optimized for the purpose of improving the efficiency of carrier injection from the electrode, and a hole transport layer composed of aromatic diamine and 8-hydroxyquinoline aluminum complex (hereinafter referred to as Alq ₃ ) As a result of the development of a device with a light-emitting layer made of a thin film between the electrodes, the luminous efficiency has been greatly improved compared to conventional devices using single crystals such as anthracene. It has been promoted with the aim of putting it into practical use as a high-performance flat panel with characteristics such as sexuality.

In addition, as an attempt to increase the light emission efficiency of the device, the use of phosphorescence instead of fluorescence has been studied. Many devices, including those provided with the hole transport layer composed of the aromatic diamine and the light-emitting layer composed of Alq ₃ described above, used fluorescent light emission. By using the light emission from the term excited state, an efficiency improvement of about 3 to 4 times is expected as compared with a conventional device using fluorescence (singlet). For this purpose, it has been studied to use a coumarin derivative or a benzophenone derivative as a light emitting layer, but only an extremely low luminance was obtained. Further, as an attempt to use the triplet state, use of a europium complex has been studied, but this has not led to highly efficient light emission. In recent years, as described in Patent Document 1, many studies have been conducted focusing on organometallic complexes such as iridium complexes for the purpose of increasing the efficiency of light emission and extending the lifetime.

WO01 / 041512A JP 2001-313178 A Japanese Unexamined Patent Publication No. 2005-162709 JP 2005-166574 A

In order to obtain high luminous efficiency, the host material to be used is important simultaneously with the dopant material. A representative example of a host material proposed is 4,4′-bis (9-carbazolyl) biphenyl (hereinafter referred to as CBP), which is a carbazole compound introduced in Patent Document 2. When CBP is used as a host material for a green phosphorescent material typified by tris (2-phenylpyridine) iridium complex (hereinafter referred to as Ir (ppy) ₃ ), CBP has a characteristic that it is easy to flow holes and electrons. The charge injection balance is lost, and excess holes flow out to the electron transport layer side. As a result, the light emission efficiency from Ir (ppy) ₃ decreases.

  As described above, in order to obtain high luminous efficiency in an organic EL device, a host material having high triplet excitation energy and balanced in both charge (hole / electron) injection and transport characteristics is required. Further, a compound that is electrochemically stable and has high heat resistance and excellent amorphous stability is desired, and further improvement is required.

  Patent Documents 3 and 4 disclose carborane compounds as shown below.

  However, the above compound is a compound in which a phenyl group, a fluorenyl group, or a carbazolylphenyl group is bonded to a carbon atom of a carborane skeleton, and a silyl group is bonded to the carbon atom of the carborane skeleton through a linking group. It is not a thing.

  In order to apply the organic EL element to a display element such as a flat panel display, it is necessary to improve the luminous efficiency of the element and at the same time sufficiently ensure stability during driving. An object of this invention is to provide the practically useful organic EL element which has high efficiency and high drive stability in view of the said present condition, and a compound suitable for it.

  As a result of intensive studies, the present inventors have found that a carborane compound having a silyl group bonded thereto via an aromatic hydrocarbon group or an aromatic heterocyclic group exhibits excellent characteristics by using it in an organic EL device. The invention has been completed.

The present invention relates to a material for an organic electroluminescent element comprising a carborane compound represented by the general formula (1).

Here, ring A represents a tetravalent carborane group of C ₂ B ₁₀ H ₈ represented by either formula (1a) or formula (1b), and is the same when a plurality of rings A are present in the molecule. It may or may not be. L ¹ is a p + 1 valent group, L ² is a q + 1 valent group, and L ¹ _and L ² are each independently a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted group. substituted aromatic heterocyclic group having 3 to 30 carbon atoms, or the aromatic hydrocarbon group and the aromatic heterocyclic aromatic group selected from the group 2-6 one linked to constructed linking aromatic group In the case of a linked aromatic group, it may be linear or branched, and the linked aromatic rings may be the same or different. R ¹ , R ² , R ³ , R ⁴ , R ⁵ and R ⁶ are each independently an aliphatic hydrocarbon group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or A substituted or unsubstituted aromatic heterocyclic group having 3 to 17 carbon atoms, R ⁷ and R ⁸ are independently hydrogen, an aliphatic hydrocarbon group having 1 to 12 carbon atoms, a substituted or unsubstituted carbon number 6 -18 aromatic hydrocarbon group or a substituted or unsubstituted C3-C17 aromatic heterocyclic group. p represents an integer of 1 to 5, q represents an integer of 0 to 5, and r represents an integer of 1 to 4.

Among the carborane compounds represented by the general formula (1), the following general formula (2) is preferable, and carborane compounds represented by the general formulas (3) and (4) are more preferable compounds.

In General Formula (2), L ¹ , L ² , R ^{1 to} R ⁸ , p, q, and r are the same as those in General Formula (1). Ring A represents a tetravalent carborane group of C ₂ B ₁₀ H ₈ represented by either formula (2a) or formula (2b), and when a plurality of rings A are present in the molecule, they may be the same May be different.

In the general formulas (3) and (4), L ¹ , L ² , R ^{1 to} R ⁸ , and p to r are the same as those in the general formula (1).

In general formulas (3) and (4), L ¹ _and L ² are each independently a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, a substituted or unsubstituted aromatic group having 3 to 17 carbon atoms. is preferably a group heterocyclic group, or the aromatic hydrocarbon group and the aromatic heterocyclic aromatic group selected from the group 2-5 one linked to constructed linking aromatic groups.

In general formulas (3) and (4), R ^{1 to} R ⁶ are each independently an aliphatic hydrocarbon group having 1 to 10 carbon atoms or a substituted or unsubstituted aromatic hydrocarbon group having 6 to 12 carbon atoms. It is preferable.

  In addition, the present invention relates to an organic electroluminescent device in which an anode, an organic layer, and a cathode are laminated on a substrate, and the organic electroluminescent device having an organic layer containing the material for an organic electroluminescent device.

  Furthermore, in the present invention, it is preferable that the organic layer containing the material for an organic electroluminescent element contains a phosphorescent dopant. It is desirable that the emission wavelength of the phosphorescent dopant has an emission maximum wavelength at 550 nm or less.

  The carborane compound used in the present invention has a structure in which a silyl group is bonded to a carborane skeleton via an aromatic hydrocarbon group or an aromatic heterocyclic group. A carborane skeleton to which an aromatic hydrocarbon group or an aromatic heterocyclic group is bonded has a high charge injection / transport capability, but it is necessary to optimize charge injection / transport properties in order to further improve device characteristics. However, it is difficult to control the distribution of molecular orbitals that are closely related to charge injection and transport properties by simply introducing other substituents onto the aromatic hydrocarbon group, aromatic heterocyclic group or carborane ring. Therefore, by introducing a substituent containing a silicon atom that can disrupt the spread of molecular orbitals, the injection and transport properties of both charges can be controlled in a more preferable range. Due to the above effects, the element driving voltage is reduced by using this for the organic EL element.

  Further, when this carborane compound is included in the light emitting layer, the charge balance becomes good, so the recombination probability is improved. Furthermore, this carborane compound has a wide band gap due to the effect of suppressing the conjugated spread of silicon atoms. Having a wide bandgap has a high enough T1 energy to confine the dopant T1 energy, since there is a correlation between the wide bandgap and the magnitude of the lowest triplet excitation energy (T1 energy). Means that For the above reasons, the transfer of T1 energy from the dopant to the host molecule can be effectively suppressed. From the above points, it is possible to achieve high luminous efficiency.

  This carborane compound has a molecular orbital distribution on each substituent due to the effect of dividing the molecular orbital spread of silicon atoms by connecting the carborane skeleton and the silyl group via an aromatic hydrocarbon group or aromatic heterocyclic group. Can be controlled. Electrochemical stability (oxidation resistance / reduction stability) is closely related to the molecular orbitals that contribute to them (highest occupied orbitals (HOMO) for oxidation, lowest orbitals (LUMO) for reduction), and the molecules themselves. In order to improve the stability against both charges, it is essential to design a molecule that distributes HOMO at sites with high oxidation resistance and LUMO at sites with high resistance to reduction. This carborane compound is considered to be able to distribute molecular orbitals to sites with high resistance to oxidation and reduction by controlling the spread of molecular orbitals as described above, and to have good charge stability. In addition, since the group connected to the silicon atom is not on the same plane, packing or interaction is difficult, and the crystallinity is low. Therefore, the phosphor element material exhibits good amorphous characteristics and high thermal stability. . That is, an element using the phosphor element material has a long driving life and can realize a highly durable organic EL element.

It is sectional drawing which shows one structural example of an organic EL element. 2 is an NMR chart of carborane compound 1. 3 is an NMR chart of carborane compound 4.

  The material for an organic electroluminescent element of the present invention is a carborane compound represented by the general formula (1). It is considered that the carborane compound has a structure substituted with an aromatic hydrocarbon group or an aromatic heterocyclic ring to which a silyl group is bonded, thereby providing the excellent effects as described above.

In General Formula (1), L ^{1 and} L ² are each independently a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms or a substituted or unsubstituted aromatic heterocyclic group having 3 to 30 carbon atoms. Or a linked aromatic group formed by linking 2 to 6 aromatic groups selected from these aromatic hydrocarbon groups and aromatic heterocyclic groups, and when linked, they may be linear It may be branched, and the aromatic rings of the aromatic groups to be connected may be the same or different. Preferably, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 17 carbon atoms, or these aromatic hydrocarbon group and aromatic heterocyclic group Is a linked aromatic group constituted by connecting 2 to 5 aromatic rings. Note that L ¹ is a p + 1 valent group, and L ² is a q + 1 valent group.

  Specific examples of the unsubstituted aromatic hydrocarbon group include aromatic hydrocarbon compounds such as benzene, naphthalene, fluorene, anthracene, phenanthrene, fluoranthene, pyrene, chrysene, and triphenylene, or aromatic hydrocarbon compounds in which a plurality of these are connected. Examples thereof include groups generated by removing hydrogen, preferably groups formed by removing hydrogen from benzene, naphthalene, anthracene, phenanthrene, and triphenylene.

  Specific examples of the unsubstituted aromatic heterocyclic group include pyridine, pyrimidine, triazine, quinoline, isoquinoline, quinoxaline, naphthyridine, carbazole, dibenzofuran, dibenzothiophene, acridine, azepine, tribenzoazepine, phenazine, phenoxazine, phenothiazine, dibenzo. Examples include aromatic heterocyclic compounds such as phosphole and dibenzoborol, or linking groups formed by removing hydrogen from an aromatic heterocyclic compound in which a plurality of these are connected, preferably pyridine, pyrimidine, triazine, carbazole, dibenzofuran, dibenzo This is a group formed by removing hydrogen from thiophene.

  A group generated by removing hydrogen from an aromatic compound having a structure in which a plurality of aromatic rings of an aromatic hydrocarbon compound or an aromatic heterocyclic compound are connected is referred to as a connected aromatic group. The linked aromatic group is a group constituted by connecting 2 to 6 aromatic rings, and the connected aromatic rings may be the same or different, and an aromatic hydrocarbon group and an aromatic heterocyclic group Both may be included. The number of connected aromatic rings is preferably 2 to 5, more preferably 2 or 3.

  Specific examples of the linked aromatic group include biphenyl, terphenyl, phenylnaphthalene, diphenylnaphthalene, phenylanthracene, diphenylanthracene, diphenylfluorene, bipyridine, bipyrimidine, vitriazine, biscarbazole, bisdibenzofuran, bisdibenzothiophene, phenylpyridine, Examples include groups formed by removing hydrogen from phenylpyrimidine, phenyltriazine, phenylcarbazole, phenyldibenzofuran, phenyldibenzothiophene, diphenylpyridine, diphenyltriazine, biscarbazolylbenzene, bisdibenzofuranylbenzene, bisdibenzothiophenylbenzene, etc. .

  The aromatic hydrocarbon group, aromatic heterocyclic group or linked aromatic group may have a substituent, and when it has a substituent, preferred substituents include an alkyl group having 1 to 12 carbon atoms, carbon It is a C1-C12 alkoxy group, a cyano group, or an acetyl group. More preferably, they are a C1-C4 alkyl group, a C1-C2 alkoxy group, or an acetyl group.

（Ａｒ¹〜Ａｒ^６は未置換の芳香族炭化水素環又は芳香族複素環）Here, in the case of the divalent group, the linked aromatic group is represented by, for example, the following formula, and may be linked in a linear or branched form.

(Ar ^{1 to} Ar ⁶ are unsubstituted aromatic hydrocarbon rings or aromatic heterocyclic rings)

  In General formula (1), p represents the integer of 1-5, Preferably it is 1-2. q is an integer of 0-5, preferably 0-2. r is an integer of 1-4, preferably 1-2.

In General Formula (1), R ^{1 to} R ⁶ are each independently an aliphatic hydrocarbon group having 1 to 12 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or an aromatic group having 3 to 17 carbon atoms. A heterocyclic group is shown. Preferably, it is a C1-C10 aliphatic hydrocarbon group or a C6-C12 aromatic hydrocarbon group. The aliphatic hydrocarbon group may be saturated or unsaturated, and may be linear, branched, or cyclic.

Specific examples of R ^{1 to} R ⁶ include an alkyl group such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a pentyl group, a hexyl group, and an octyl group, a cycloalkyl group such as a cyclopentyl group and a cyclohexyl group, Aromatic hydrocarbon groups such as phenyl group, pyridyl group, pyrimidyl group, triazyl group, naphthyl group, quinolyl group, isoquinolyl group, quinazolyl group, phthalazyl group, fluorenyl group, carbazolyl group, dibenzofuranyl group, dibenzothiophenyl group or the like An aromatic heterocyclic group is mentioned. Preferable examples include phenyl group, pyridyl group, pyrimidyl group, triazyl group, naphthyl group, quinolyl group, isoquinolyl group, fluorenyl group, and carbazolyl group.
These may further have a substituent, and preferable substituents are alkyl groups having 1 to 4 carbon atoms, alkoxy groups having 1 to 2 carbon atoms, acetyl groups, cyano groups, and aromatic hydrocarbons having 6 to 12 carbon atoms. Group, an aromatic heterocyclic group having 3 to 12 carbon atoms, and specific examples include methyl group, ethyl group, isopropyl group, butyl group, methoxy group, ethoxy group, acetyl group, phenyl group, pyridyl group, pyrimidyl group , Triazyl group, naphthyl group, quinolyl group, isoquinolyl group, fluorenyl group, carbazolyl group, dibenzofuranyl group, dibenzothiophenyl group, cyano group.

In the general formula (1), R ⁷ and R ⁸ are each independently hydrogen, an aliphatic hydrocarbon group having 1 to 12 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or an aromatic group having 3 to 17 carbon atoms. Represents a heterocyclic group. Preferably, it is hydrogen, an aliphatic hydrocarbon group having 1 to 8 carbon atoms, an aromatic hydrocarbon group having 6 to 12 carbon atoms or an aromatic heterocyclic group having 3 to 12 carbon atoms, except that it contains hydrogen, it is similar to those described for the ^R 1 to R ^6.

In general formula (1), ring A represents a tetravalent carborane group of C ₂ B ₁₀ H ₈ represented by either formula (1a) or formula (1b), and there are a plurality of rings A in the molecule. The cases may be the same or different. The four bonds in formula (1a) or formula (1b) may originate from C or B, but the bonds that bind to L ¹ or L ² preferably originate from C.

  Among the carborane compounds represented by the general formula (1), a carborane compound represented by the above general formula (2) can be mentioned as a preferred compound, preferably the above general formula (3) or (4), more preferably the above. Examples thereof include carborane compounds represented by the general formula (3).

  In general formulas (1) to (4), except for ring A, the same symbols and formulas are understood to have the same meaning unless otherwise specified. Ring A differs in that the meaning in general formula (2) is more limited than in general formula (1).

  The carborane compounds represented by the general formulas (1) to (4) can be synthesized using a known method by selecting raw materials according to the structure of the target compound.

(A-1) can be synthesized by the following reaction formula with reference to synthesis examples shown in Journal of Organometallic Chemistry, 1993, 462, p19-29.

(A-2) can be synthesized by the following reaction formula with reference to synthesis examples shown in Journal of Organic Chemistry, 2007, 72, p6241-6246.

(A-3) can be synthesized by the following reaction formula with reference to synthesis examples shown in European Journal of Inorganic Chemistry, 2010, p2012-2024 and Inorganic Chemistry, 1995, 34, p2095-2100.

(A-4) can be synthesized by the following reaction formula with reference to the synthesis example shown in Inorganica Chimica Acta, 1995, 240, p371-378.

  Specific examples of the carborane compounds represented by the general formulas (1) to (4) are shown below, but the organic electroluminescent element material of the present invention is not limited thereto.

  The organic electroluminescent element material of the present invention contains an excellent organic electroluminescent element by containing it in at least one organic layer of an organic EL element in which an anode, a plurality of organic layers and a cathode are laminated on a substrate. give. As the organic layer to be contained, a light emitting layer, an electron transport layer or a hole blocking layer is suitable. Here, when used in a light emitting layer, it can be used as a host material of a light emitting layer containing a fluorescent, delayed fluorescent or phosphorescent dopant, and the compound of the present invention emits fluorescence and delayed fluorescence. It can be used as an organic light emitting material. When used as an organic light-emitting material that emits fluorescence and delayed fluorescence, another organic compound having at least one of excited singlet energy and excited triplet energy higher than that of the compound of the present invention is used as a host material. It is preferable. The compound of the present invention is particularly preferably contained as a host material for a light emitting layer containing a phosphorescent dopant.

  Next, the organic EL element using the organic electroluminescent element material of the present invention will be described.

  The organic EL device of the present invention has an organic layer having at least one light emitting layer between an anode and a cathode laminated on a substrate, and the at least one organic layer is for the organic electroluminescent device of the present invention. Contains materials. Advantageously, the organic electroluminescent device material of the present invention is included in the light emitting layer together with a phosphorescent dopant.

  Next, the structure of the organic EL element of the present invention will be described with reference to the drawings. However, the structure of the organic EL element of the present invention is not limited to the illustrated one.

  FIG. 1 is a cross-sectional view showing a structural example of a general organic EL device used in the present invention, wherein 1 is a substrate, 2 is an anode, 3 is a hole injection layer, 4 is a hole transport layer, and 5 is a light emitting layer. , 6 represents an electron transport layer, and 7 represents a cathode. The organic EL device of the present invention may have an exciton blocking layer adjacent to the light emitting layer, and may have an electron blocking layer between the light emitting layer and the hole injection layer. The exciton blocking layer can be inserted on either the anode side or the cathode side of the light emitting layer, or both can be inserted simultaneously. The organic EL device of the present invention has a substrate, an anode, a light emitting layer and a cathode as essential layers, but it is preferable to have a hole injecting and transporting layer and an electron injecting and transporting layer in layers other than the essential layers, and further emit light. It is preferable to have a hole blocking layer between the layer and the electron injecting and transporting layer. The hole injection / transport layer means either or both of a hole injection layer and a hole transport layer, and the electron injection / transport layer means either or both of an electron injection layer and an electron transport layer.

  In addition, it is also possible to laminate | stack the cathode 7, the electron carrying layer 6, the light emitting layer 5, the positive hole transport layer 4, and the anode 2 in order on the board | substrate 1 in the reverse structure, FIG. Layers can be added or omitted as necessary.

-Board-
The organic EL element of the present invention is preferably supported on a substrate. The substrate is not particularly limited as long as it is conventionally used for an organic EL element. For example, a substrate made of glass, transparent plastic, quartz, or the like can be used.

-Anode-
As the anode in the organic EL element, an electrode material made of a metal, an alloy, an electrically conductive compound, or a mixture thereof having a high work function (4 eV or more) is preferably used. Specific examples of such an electrode substance include conductive transparent materials such as metals such as Au, CuI, indium tin oxide (ITO), SnO ₂ , and ZnO. Alternatively, an amorphous material such as IDIXO (In ₂ O ₃ —ZnO) capable of forming a transparent conductive film may be used. For the anode, these electrode materials may be formed into a thin film by a method such as vapor deposition or sputtering, and a pattern having a desired shape may be formed by a photolithography method. ), A pattern may be formed through a mask having a desired shape when the electrode material is deposited or sputtered. Or when using the substance which can be apply | coated like an organic electroconductivity compound, wet film-forming methods, such as a printing system and a coating system, can also be used. When light emission is extracted from the anode, it is desirable that the transmittance be greater than 10%, and the sheet resistance as the anode is preferably several hundred Ω / □ or less. Further, although the film thickness depends on the material, it is usually selected in the range of 10 to 1000 nm, preferably 10 to 200 nm.

-Cathode-
On the other hand, as the cathode, a material having a low work function (4 eV or less) metal (referred to as an electron injecting metal), an alloy, an electrically conductive compound, and a mixture thereof as an electrode material is used. Specific examples of such electrode materials include sodium, sodium-potassium alloy, magnesium, lithium, magnesium / copper mixture, magnesium / silver mixture, magnesium / aluminum mixture, magnesium / indium mixture, aluminum / aluminum oxide (Al ₂ O ₃ ) Mixtures, indium, lithium / aluminum mixtures, rare earth metals and the like. Among these, from the point of durability against electron injection and oxidation, etc., a mixture of an electron injecting metal and a second metal which is a stable metal having a larger work function than this, for example, a magnesium / silver mixture, Magnesium / aluminum mixtures, magnesium / indium mixtures, aluminum / aluminum oxide (Al ₂ O ₃ ) mixtures, lithium / aluminum mixtures, aluminum and the like are preferred. The cathode can be produced by forming a thin film of these electrode materials by a method such as vapor deposition or sputtering. The sheet resistance as the cathode is preferably several hundred Ω / □ or less, and the film thickness is usually selected in the range of 10 nm to 5 μm, preferably 50 to 200 nm. In order to transmit the emitted light, if either one of the anode or the cathode of the organic EL element is transparent or translucent, the light emission luminance is improved, which is convenient.

  Moreover, after producing the metal with a film thickness of 1 to 20 nm on the cathode, a transparent or translucent cathode can be produced by producing the conductive transparent material mentioned in the description of the anode on the cathode, By applying this, an element in which both the anode and the cathode are transmissive can be manufactured.

-Light emitting layer-
The light emitting layer is a layer that emits light after excitons are generated by recombination of holes and electrons injected from the anode and the cathode, respectively, and the light emitting layer includes an organic light emitting material and a host material.
When the light emitting layer is a fluorescent light emitting layer, the fluorescent light emitting material may be at least one kind of fluorescent light emitting material, but it is preferable to use the fluorescent light emitting material as a fluorescent light emitting dopant and include a host material. .

  As the fluorescent light-emitting material in the light-emitting layer, a carborane compound represented by the general formula (1) can be used, but since it is known from many patent documents and the like, it can also be selected from them. For example, benzoxazole derivatives, benzothiazole derivatives, benzimidazole derivatives, styrylbenzene derivatives, polyphenyl derivatives, diphenylbutadiene derivatives, tetraphenylbutadiene derivatives, naphthalimide derivatives, coumarin derivatives, condensed aromatic compounds, perinone derivatives, oxadiazole derivatives , Oxazine derivatives, aldazine derivatives, pyralidine derivatives, cyclopentadiene derivatives, bisstyrylanthracene derivatives, quinacridone derivatives, pyrrolopyridine derivatives, thiadiazolopyridine derivatives, styrylamine derivatives, diketopyrrolopyrrole derivatives, aromatic dimethylolidine compounds, 8-quinolinol Polythiophene such as metal complexes of derivatives, metal complexes of pyromethene derivatives, various metal complexes represented by rare earth complexes, transition metal complexes, etc. , Polyphenylene, polyphenylene vinylene polymer compounds such as, organic silane derivatives, and the like. Preferred examples include condensed aromatic compounds, styryl compounds, diketopyrrolopyrrole compounds, oxazine compounds, pyromethene metal complexes, transition metal complexes, and lanthanoid complexes, more preferably naphthacene, pyrene, chrysene, triphenylene, benzo [c] phenanthrene, Benzo [a] anthracene, pentacene, perylene, fluoranthene, acenaphthofluoranthene, dibenzo [a, j] anthracene, dibenzo [a, h] anthracene, benzo [a] naphthacene, hexacene, anthanthrene, naphtho [2,1 -f] isoquinoline, α-naphthaphenanthridine, phenanthrooxazole, quinolino [6,5-f] quinoline, benzothiophanthrene and the like. These may have an alkyl group, an aryl group, an aromatic heterocyclic group, or a diarylamino group as a substituent.

  As the fluorescent host material in the light emitting layer, a carborane compound represented by the general formula (1) can be used, but since it is known from many patent documents, it can be selected from them. For example, a compound having a condensed aryl ring such as naphthalene, anthracene, phenanthrene, pyrene, chrysene, naphthacene, triphenylene, perylene, fluoranthene, fluorene, indene, or a derivative thereof, N, N′-dinaphthyl-N, N′-diphenyl-4 Aromatic amine derivatives such as 4,4'-diphenyl-1,1'-diamine, metal chelated oxinoid compounds such as tris (8-quinolinato) aluminum (III), bisstyryl derivatives such as distyrylbenzene derivatives, tetraphenyl Butadiene derivatives, indene derivatives, coumarin derivatives, oxadiazole derivatives, pyrrolopyridine derivatives, perinone derivatives, cyclopentadiene derivatives, pyrrolopyrrole derivatives, thiadiazolopyridine derivatives, dibenzofuran derivatives, Carbazole derivatives, indolocarbazole derivatives, triazine derivatives, in polymer systems, a polyphenylene vinylene derivative, polyparaphenylene derivatives, polyfluorene derivatives, polyvinylcarbazole derivatives, polythiophene derivatives can be used is not particularly limited.

  When the fluorescent light emitting material is used as a fluorescent light emitting dopant and includes a host material, the amount of the fluorescent light emitting dopant contained in the light emitting layer is 0.01 to 20% by weight, preferably 0.1 to 10% by weight. It should be in range.

  Usually, an organic EL element injects electric charges into a luminescent material from both an anode and a cathode, generates an excited luminescent material, and emits light. In the case of a charge injection type organic EL device, it is said that 25% of the generated excitons are excited to a singlet excited state and the remaining 75% are excited to a triplet excited state. As shown in Advanced Materials 2009, 21, 4802-4806. Certain fluorescent materials emit triplet-triplet annihilation or heat after energy transition to triplet excited state due to intersystem crossing. It is known that, due to the absorption of energy, the singlet excited state is crossed back to back and emits fluorescence, thereby expressing thermally activated delayed fluorescence. The organic EL device of the present invention can also exhibit delayed fluorescence. In this case, both fluorescence emission and delayed fluorescence emission can be included. However, light emission from the host material may be partly or partly emitted.

  When the light emitting layer is a delayed fluorescent light emitting layer, the delayed light emitting material may use at least one delayed light emitting material alone, but the delayed fluorescent material is used as a delayed fluorescent light emitting dopant and includes a host material. Is preferred.

  As the delayed fluorescent light emitting material in the light emitting layer, a carborane compound represented by the general formula (1) can be used, but it can also be selected from known delayed fluorescent light emitting materials. For example, a tin complex, an indolocarbazole derivative, a copper complex, a carbazole derivative, and the like can be given. Specific examples include compounds described in the following non-patent documents and patent documents, but are not limited to these compounds.

  1) Adv. Mater. 2009, 21, 4802-4806, 2) Appl. Phys. Lett. 98, 083302 (2011), 3) JP 2011-213643, 4) J. Am. Chem. Soc. 2012 , 134, 14706-14709.

  Specific examples of the delayed light emitting material are shown below, but are not limited to the following compounds.

  When the delayed fluorescent material is used as a delayed fluorescent material and includes a host material, the amount of the delayed fluorescent material contained in the light emitting layer is 0.01 to 50% by weight, preferably 0.1 to 20%. It is good to be in the range of% by weight, more preferably 0.01 to 10%.

  As the delayed fluorescent host material in the light emitting layer, a carborane compound represented by the general formula (1) can be used, but it can also be selected from compounds other than carborane. For example, a compound having a condensed aryl ring such as naphthalene, anthracene, phenanthrene, pyrene, chrysene, naphthacene, triphenylene, perylene, fluoranthene, fluorene, indene, or a derivative thereof, N, N′-dinaphthyl-N, N′-diphenyl-4 Aromatic amine derivatives such as 4,4'-diphenyl-1,1'-diamine, metal chelated oxinoid compounds such as tris (8-quinolinato) aluminum (III), bisstyryl derivatives such as distyrylbenzene derivatives, tetraphenyl Butadiene derivatives, indene derivatives, coumarin derivatives, oxadiazole derivatives, pyrrolopyridine derivatives, perinone derivatives, cyclopentadiene derivatives, pyrrolopyrrole derivatives, thiadiazolopyridine derivatives, dibenzofuran derivatives, In the rubazole derivative, indolocarbazole derivative, triazine derivative, and polymer system, polyphenylene vinylene derivative, polyparaphenylene derivative, polyfluorene derivative, polyvinylcarbazole derivative, polythiophene derivative, arylsilane derivative, and the like can be used, but are not particularly limited. .

  When the light emitting layer is a phosphorescent light emitting layer, the light emitting layer includes a phosphorescent light emitting dopant and a host material. The phosphorescent dopant material preferably contains an organometallic complex containing at least one metal selected from ruthenium, rhodium, palladium, silver, rhenium, osmium, iridium, platinum and gold. Specific examples include compounds described in the following patent documents, but are not limited to these compounds.

  WO2009 / 073245, WO2009 / 046266, WO2007 / 095118, WO2008 / 156879, WO2008 / 140657, US2008 / 261076, and the like.

Preferable phosphorescent dopants include complexes such as Ir (ppy) ₃ having a noble metal element of Ir such as the central metal, Ir (bt) complexes such as ₂ · acac _3, complexes such as PtOEt ₃ and the like. Specific examples of these complexes are shown below, but are not limited to the following compounds.

  The amount of the phosphorescent dopant contained in the light emitting layer is 2 to 40% by weight, preferably 5 to 30% by weight.

  When the light emitting layer is a phosphorescent light emitting layer, the carborane compound represented by the general formula (1) according to the present invention is preferably used as the host material in the light emitting layer. However, when the carborane compound is used in any organic layer other than the light-emitting layer, the material used for the light-emitting layer may be a host material other than the carborane compound. Moreover, you may use together a carborane compound and another host material. Furthermore, a plurality of known host materials may be used in combination.

  The known host compound that can be used is preferably a compound that has a hole transporting ability and an electron transporting ability, prevents light emission from becoming longer, and has a high glass transition temperature.

  Such other host materials are known from numerous patent documents and the like, and can be selected from them. Specific examples of the host material are not particularly limited, but include indole derivatives, carbazole derivatives, triazole derivatives, oxazole derivatives, oxadiazole derivatives, imidazole derivatives, polyarylalkane derivatives, pyrazoline derivatives, pyrazolone derivatives, phenylenediamine. Derivatives, arylamine derivatives, amino-substituted chalcone derivatives, styrylanthracene derivatives, fluorenone derivatives, hydrazone derivatives, stilbene derivatives, silazane derivatives, aromatic tertiary amine compounds, styrylamine compounds, aromatic dimethylidene compounds, porphyrin compounds, anthraquino Heterocyclic tetracarboxylic acid anhydrides such as dimethane derivatives, anthrone derivatives, diphenylquinone derivatives, thiopyran dioxide derivatives, naphthalene perylene, Various metal complexes represented by metal complexes of Russianin derivatives, 8-quinolinol derivatives, metal phthalocyanines, metal complexes of benzoxazole and benzothiazole derivatives, polysilane compounds, poly (N-vinylcarbazole) derivatives, aniline copolymers, Examples thereof include polymer compounds such as thiophene oligomers, polythiophene derivatives, polyphenylene derivatives, polyphenylene vinylene derivatives, polyfluorene derivatives, and the like.

  The light emitting layer may be a fluorescent light emitting layer, a delayed fluorescent light emitting layer, or a phosphorescent light emitting layer, but is preferably a phosphorescent light emitting layer.

-Injection layer-
The injection layer is a layer provided between the electrode and the organic layer for lowering the driving voltage and improving the luminance of light emission. There are a hole injection layer and an electron injection layer, and between the anode and the light emitting layer or the hole transport layer. And between the cathode and the light emitting layer or the electron transport layer. The injection layer can be provided as necessary.

-Hole blocking layer-
The hole blocking layer has a function of an electron transport layer in a broad sense, and is made of a hole blocking material that has a function of transporting electrons and has a remarkably small ability to transport holes. The probability of recombination of electrons and holes can be improved by blocking.

  It is preferable to use the carborane compound represented by the general formula (1) according to the present invention for the hole blocking layer. However, when the carborane compound is used for any other organic layer, a known hole blocking layer is used. Materials may be used. Moreover, as a hole-blocking layer material, the material of the electron carrying layer mentioned later can be used as needed.

-Electron blocking layer-
The electron blocking layer is made of a material that has a function of transporting holes and has a very small ability to transport electrons. The electron blocking layer blocks the electrons while transporting holes, and the probability of recombination of electrons and holes. Can be improved.

  As a material for the electron blocking layer, a material for a hole transport layer described later can be used as necessary. The thickness of the electron blocking layer is preferably 3 to 100 nm, more preferably 5 to 30 nm.

-Exciton blocking layer-
The exciton blocking layer is a layer for preventing excitons generated by recombination of holes and electrons in the light emitting layer from diffusing into the charge transport layer. It becomes possible to efficiently confine in the light emitting layer, and the light emission efficiency of the device can be improved. The exciton blocking layer can be inserted on either the anode side or the cathode side adjacent to the light emitting layer, or both can be inserted simultaneously.

  As the material for the exciton blocking layer, a carborane compound represented by the general formula (1) can be used. As other materials, for example, 1,3-dicarbazolylbenzene (mCP), bis ( 2-methyl-8-quinolinolato) -4-phenylphenolato aluminum (III) (BAlq).

-Hole transport layer-
The hole transport layer is made of a hole transport material having a function of transporting holes, and the hole transport layer can be provided as a single layer or a plurality of layers.

  The hole transport material has any of hole injection or transport and electron barrier properties, and may be either organic or inorganic. As the known hole transporting material that can be used, a carborane compound represented by the general formula (1) is preferably used, but any one of conventionally known compounds can be selected and used. Known hole transporting materials that can be used include, for example, triazole derivatives, oxadiazole derivatives, imidazole derivatives, polyarylalkane derivatives, pyrazoline derivatives and pyrazolone derivatives, phenylenediamine derivatives, arylamine derivatives, amino-substituted chalcone derivatives, oxazole derivatives. , Styrylanthracene derivatives, fluorenone derivatives, hydrazone derivatives, stilbene derivatives, silazane derivatives, aniline copolymers, conductive polymer oligomers, particularly thiophene oligomers, etc., but porphyrin compounds, aromatic tertiary amine compounds and It is preferable to use a styrylamine compound, and it is more preferable to use an aromatic tertiary amine compound.

-Electron transport layer-
The electron transport layer is made of a material having a function of transporting electrons, and the electron transport layer can be provided as a single layer or a plurality of layers.

  The electron transport material (which may also serve as a hole blocking material) may have a function of transmitting electrons injected from the cathode to the light emitting layer. Although it is preferable to use the carborane derivative represented by the general formula (1) according to the present invention for the electron transport layer, any one of conventionally known compounds can be selected and used. Fluorene derivatives, diphenylquinone derivatives, thiopyran dioxide derivatives, carbodiimides, fluorenylidenemethane derivatives, anthraquinodimethane and anthrone derivatives, oxadiazole derivatives and the like can be mentioned. Furthermore, in the above oxadiazole derivative, a thiadiazole derivative in which the oxygen atom of the oxadiazole ring is substituted with a sulfur atom, and a quinoxaline derivative having a quinoxaline ring known as an electron withdrawing group can also be used as an electron transport material. Furthermore, a polymer material in which these materials are introduced into a polymer chain or these materials are used as a polymer main chain can also be used.

  Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is of course not limited to these examples, and can be implemented in various forms as long as the gist thereof is not exceeded. .

In addition, the value of T1 energy as used in the present specification is a value obtained using Gaussian 09, which is molecular calculation software manufactured by Gaussian, USA, and is a value calculated by B3LYP / 6-31G ^* level structure optimization calculation. It is defined as

  A carborane compound as a material for an organic electroluminescence device was synthesized by the following route. The compound number corresponds to the number given to the above chemical formula.

Example 1
Compound 1 is synthesized according to the following reaction formula.

  Under a nitrogen atmosphere, 6.92 g (0.0480 mol) of m-carborane and 183 mL of 1,2-dimethoxyethane (DME) were added, and the DME solution was cooled to 0 ° C. 61.1 mL of a 1.65 M n-butyllithium hexane solution was dropped, and the mixture was stirred at room temperature for 15 minutes. After adding 9.5 g (0.0960 mol) of copper (I) chloride and stirring at room temperature for 15 minutes, 28.7 mL of pyridine was added. After stirring at room temperature for 5 minutes, 28.5 g (0.101 mol) of p-bromoiodobenzene was added and stirred overnight at 95 ° C. Dichloromethane (500 mL) and 1N hydrochloric acid (500 mL) were added to the resulting reaction solution with stirring, and the organic layer was washed with distilled water (3 × 500 mL). After the organic layer was dried over anhydrous magnesium sulfate, magnesium sulfate was filtered off and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 13.7 g (30.2 mmol, yield 63%) of intermediate A.

Under a nitrogen atmosphere, Intermediate A was dissolved in 8.6 g (0.0189 mol), tetrahydrofuran (THF) in 17 mL, and diethyl ether in 60 mL, and cooled to -30 ° C. Thereafter, 25 mL of a 1.65 M n-butyllithium hexane solution was dropped, and the mixture was stirred at room temperature for 1 hour. To the resulting white solution was added dropwise 11.6 g (0.0393 mol) of triphenylchlorosilane dissolved in 34 ml of THF and 24 ml of diethyl ether. Then, the mixture was stirred overnight while gradually warming to room temperature. Dichloromethane (300 mL) and 1N hydrochloric acid (200 mL) were added to the resulting reaction mixture with stirring, and the organic layer was distilled water (3 × 500 mL). Washed with. After the organic layer was dried over anhydrous magnesium sulfate, magnesium sulfate was filtered off and the solvent was distilled off under reduced pressure. The obtained residue was purified by crystallization to obtain 3.56 g (4.38 mmol, yield 23%) of Compound 1 as a white solid. FD-MS, m / z 813 [M] ⁺ , ¹ H-NMR measurement results (measuring solvent: CDCl ₃ ) are shown in FIG.

Example 2
Compound 4 is synthesized according to the following reaction formula.

  Under a nitrogen atmosphere, 63.6 g (0.268 mol) of 2,6-dibromopyridine and 1080 mL of THF were added and cooled to -50 ° C. Thereafter, a 2.69 M n-butyllithium hexane solution was added dropwise, and the mixture was stirred at −50 ° C. for 2 hours. To the resulting black solution, 78.4 g (0.266 mol) of triphenylchlorosilane dissolved in 240 ml of THF and 160 ml of diethyl ether was added dropwise. Then, the mixture was stirred overnight while gradually warming to room temperature. Ethyl acetate (1000 mL) and 1N hydrochloric acid (1000 mL) were added to the resulting reaction mixture with stirring, and the organic layer was distilled water (3 × 500 mL). ). After the organic layer was dried over anhydrous magnesium sulfate, magnesium sulfate was filtered off and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 18.5 g (44.4 mmol, 17% yield) of Intermediate B as a white solid.

Under a nitrogen atmosphere, m-carborane 2.6 g (0.0185 mol) and 1,2-dimethoxyethane (DME) 80 mL were added, and the mixture was stirred at room temperature for 5 minutes. 27.4 mL of a 1.59 M n-butyllithium hexane solution was dropped, and the mixture was stirred at room temperature for 5 minutes. Thereafter, 11 mL of pyridine and 5.9 g (0.0592 mol) of copper (I) chloride were added, and the mixture was stirred at 60 ° C. for 1 hour. To the obtained black solution, 17.0 g (0.0408 mol) of Intermediate B dissolved in 40 mL of DME was added dropwise, and the mixture was stirred at 90 ° C. overnight. Dichloromethane (500 mL) and 1N hydrochloric acid (500 mL) were added to the resulting reaction solution with stirring, and the organic layer was washed with distilled water (3 × 500 mL). After the organic layer was dried over anhydrous magnesium sulfate, magnesium sulfate was filtered off and the solvent was distilled off under reduced pressure. The obtained residue was crystallized and purified by silica gel column chromatography to obtain 1.9 g (2.33 mmol, yield 13%) of compound 4. APCI-TOFMS, m / z 816 [M + H] ⁺ , ¹ H-NMR measurement results (measurement solvent: CDCl ₃ ) are shown in FIG.

Reference example 1
Table 1 shows the results of calculating the T1 energy of the carborane compound using Gaussian09.

Chemical formulas of compounds H-1 to H-3 for comparison are shown below.

  From Table 1, it was confirmed that the T1 energy value is increased by bonding a silyl group to the carborane skeleton via an aromatic hydrocarbon group or an aromatic heterocyclic group.

  Moreover, the organic EL element was produced using the compound 1,2,4,5,6,8,13,32 and H-1, H-2, H-3.

Example 3
Each thin film was laminated at a vacuum degree of 2.0 × 10 ⁻⁵ Pa by a vacuum deposition method on a glass substrate on which an anode made of indium tin oxide (ITO) having a thickness of 70 nm was formed. First, copper phthalocyanine (CuPC) was formed to a thickness of 30 nm on ITO as a hole injection layer. Next, N, N′-di (1-naphthyl) -N, N′-diphenylbenzidine (α-NPD) was formed to a thickness of 15 nm as a hole transport layer. Next, on the hole transport layer, Compound 1 as a host material of the light emitting layer and an iridium complex [iridium (III) bis (4,6-di-fluorophenyl) -pyridinate-N as a blue phosphorescent material as a dopant , C2 ′] picolinate] (FIrpic) were co-deposited from different deposition sources to form a light emitting layer with a thickness of 30 nm. The concentration of FIrpic was 10%. Next, Alq ₃ was formed to a thickness of 25 nm as an electron transport layer. Further, on the electron transport layer, lithium fluoride (LiF) was formed to a thickness of 1.0 nm as an electron injection layer. Finally, aluminum (Al) was formed as an electrode to a thickness of 70 nm on the electron injection layer. The obtained organic EL device has a layer structure in which an electron injection layer is added between the cathode and the electron transport layer in the organic EL device shown in FIG.

When an external power source was connected to the obtained organic EL element and a DC voltage was applied, it was confirmed that the organic EL element had light emission characteristics as shown in Table 2. In Table 2, the luminance, voltage, and luminous efficiency show values (initial characteristics) at 2.5 mA / cm ² . The maximum wavelength of the device emission spectrum was 475 nm, indicating that light emission from FIrpic was obtained.

Examples 4-9
An organic EL device was produced in the same manner as in Example 3 except that compounds 2, 4, 5, 6, 8, and 32 were used in place of compound 1 as the host material of the light emitting layer in example 3.

Comparative Example 1
An organic EL device was produced in the same manner as in Example 3 except that mCP was used as the host material of the light emitting layer in Example 3.

Comparative Examples 2-4
An organic EL device was produced in the same manner as in Example 3, except that Compound H-1, H-2, or H-3 was used as the host material for the light emitting layer in Example 3.

  When the organic EL devices obtained in Examples 4 to 9 and Comparative Examples 1 to 4 were evaluated in the same manner as in Example 3, it was confirmed that the organic EL elements had light emission characteristics as shown in Table 2. In addition, the maximum wavelength of the emission spectrum of the organic EL elements obtained in Examples 4 to 9 and Comparative Examples 1 to 4 was 475 nm, and it was identified that light emission from FIrpic was obtained.

  From Table 2, in Examples 3-9, when the carborane compound of this invention is used for a light emitting layer, the luminous efficiency has shown the favorable characteristic compared with Comparative Examples 1-4.

Example 10
Each thin film was laminated at a vacuum degree of 2.0 × 10 ⁻⁵ Pa by a vacuum deposition method on a glass substrate on which an anode made of ITO having a thickness of 70 nm was formed. First, CuPC was formed to a thickness of 30 nm on ITO as a hole injection layer. Next, α-NPD was formed to a thickness of 15 nm as a hole transport layer. Next, on the hole transport layer, Compound 1 as the host material of the light emitting layer and Ir (ppy) ₃ as the dopant were co-deposited from different vapor deposition sources to form a light emitting layer with a thickness of 30 nm. . The concentration of Ir (ppy) ₃ was 10%. Next, Alq ₃ was formed to a thickness of 25 nm as an electron transport layer. Further, LiF was formed to a thickness of 1 nm as an electron injection layer on the electron transport layer. Finally, Al was formed as an electrode to a thickness of 70 nm on the electron injection layer, and an organic EL device was produced.

When an external power source was connected to the obtained organic EL element and a DC voltage was applied, it was confirmed that the organic EL element had light emission characteristics as shown in Table 3. In Table 3, the brightness, voltage, and luminous efficiency show values (initial characteristics) when driven at 20 mA / cm ² . The maximum wavelength of the device emission spectrum was 530 nm, and it was found that light emission from Ir (ppy) ₃ was obtained.

Examples 11-17
An organic EL device was produced in the same manner as in Example 10 except that compounds 2, 4, 5, 6, 8, 13, and 32 were used in place of compound 1 as the host material of the light emitting layer in example 10.

Comparative Examples 5-8
An organic EL device was produced in the same manner as in Example 10 except that CBP, H-1, H-2, or H-3 was used as the host material of the light emitting layer in Example 10.

When the organic EL elements obtained in Examples 11 to 17 and Comparative Examples 5 to 8 were evaluated in the same manner as in Example 10, it was confirmed that the organic EL elements had light emission characteristics as shown in Table 3. In addition, the maximum wavelength of the emission spectrum of the organic EL elements obtained in Examples 11 to 17 and Comparative Examples 5 to 8 was 530 nm, and it was identified that light emission from Ir (ppy) ₃ was obtained.

  From Table 3, when the carborane compound of this invention is used for a light emitting layer (Examples 10-17), compared with the case other than that (Comparative Examples 5-8), the favorable luminous efficiency is shown.

Example 18
Each thin film was laminated at a vacuum degree of 2.0 × 10 ⁻⁵ Pa by a vacuum deposition method on a glass substrate on which an anode made of ITO having a thickness of 70 nm was formed. First, CuPC was formed to a thickness of 30 nm on ITO as a hole injection layer. Next, α-NPD was formed to a thickness of 15 nm as a hole transport layer. Next, CBP as a host material of the light emitting layer and Ir (ppy) ₃ as a dopant were co-deposited on the hole transport layer from different vapor deposition sources to form a light emitting layer with a thickness of 30 nm. The concentration of Ir (ppy) ₃ was 10%. Next, Compound 1 having a thickness of 5 nm was formed as a hole blocking layer on the light emitting layer. Next, Alq ₃ was formed to a thickness of 20 nm as an electron transport layer. Furthermore, LiF was formed to a thickness of 1.0 nm as an electron injection layer on the electron transport layer. Finally, Al was formed as an electrode to a thickness of 70 nm on the electron injection layer. The obtained organic EL device has a layer structure in which an electron injection layer is added between the cathode and the electron transport layer and a hole blocking layer is added between the light emitting layer and the electron transport layer in the organic EL device shown in FIG. Have

When an external power source was connected to the obtained organic EL element and a DC voltage was applied, it was confirmed that the organic EL element had the light emission characteristics as shown in Table 4. In Table 4, the brightness, voltage, and luminous efficiency show values (initial characteristics) when driven at 20 mA / cm ² . The maximum wavelength of the device emission spectrum was 530 nm, and it was found that light emission from Ir (ppy) ₃ was obtained.

Examples 19-25
An organic EL device was produced in the same manner as in Example 18 except that compounds 2, 4, 5, 6, 8, 13, and 32 were used as the hole blocking material in Example 18 instead of Compound 1.

Comparative Example 9
An organic EL device was produced in the same manner as in Example 18 except that the film thickness of Alq ₃ as the electron transport layer in Example 18 was 25 nm and no hole blocking layer was provided.

Comparative Examples 10-12
An organic EL device was produced in the same manner as in Example 18 except that Compound H-1, H-2, or H-3 was used as the hole blocking material in Example 18.

The organic EL devices obtained in Examples 19 to 25 and Comparative Examples 9 to 12 were evaluated in the same manner as in Example 18. As a result, it was confirmed that the organic EL elements had light emission characteristics as shown in Table 4. In addition, the maximum wavelength of the emission spectrum of the organic EL elements obtained in Examples 19 to 25 and Comparative Examples 9 to 12 was 530 nm, and it was identified that light emission from Ir (ppy) ₃ was obtained. The host material of the light emitting layer used in Examples 19 to 25 and Comparative Examples 9 to 12 is CBP.

  From Table 4, the initial characteristics were improved in all systems as compared to cases other than Comparative Example 9 (when no hole blocking material was used). Above all, when the carborane compound of the present invention is used for the hole blocking layer, it shows better characteristics than other cases (Comparative Examples 10 to 12).

Industrial applicability

  The organic EL device according to the present invention has practically satisfactory levels in terms of light emission characteristics, driving life and durability, flat panel display (mobile phone display device, in-vehicle display device, OA computer display device, television, etc.), surface light emission, etc. Its technical value is great in applications to light sources (lighting, light sources for copying machines, backlight light sources for liquid crystal displays and instruments), display boards, and sign lamps that make use of the characteristics of the body.

Claims (9)

A material for an organic electroluminescence device comprising a carborane compound represented by the general formula (1).

Here, ring A represents a tetravalent carborane group of C ₂ B ₁₀ H ₈ represented by either formula (1a) or formula (1b), and is the same when a plurality of rings A are present in the molecule. It may or may not be. L ¹ is a p + 1 valent group, L ² is a q + 1 valent group, and L ¹ _and L ² are each independently a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted group. substituted aromatic heterocyclic group having 3 to 30 carbon atoms, or the aromatic hydrocarbon group and the aromatic heterocyclic aromatic group selected from the group 2-6 one linked to constructed linking aromatic group In the case of a linked aromatic group, it may be linear or branched, and the linked aromatic rings may be the same or different. R ¹ , R ² , R ³ , R ⁴ , R ⁵ and R ⁶ are each independently an aliphatic hydrocarbon group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or A substituted or unsubstituted aromatic heterocyclic group having 3 to 17 carbon atoms, R ⁷ and R ⁸ are independently hydrogen, an aliphatic hydrocarbon group having 1 to 12 carbon atoms, a substituted or unsubstituted carbon number 6 -18 aromatic hydrocarbon group or a substituted or unsubstituted C3-C17 aromatic heterocyclic group. p represents an integer of 1 to 5, q represents an integer of 0 to 5, and r represents an integer of 1 to 4. The organic electroluminescent element material according to claim 1, wherein the carborane compound is a carborane compound represented by the general formula (2).

Here, L ¹ , L ² , R ^{1 to} R ⁸ , p, q, and r are the same as those in the general formula (1). Ring A represents a tetravalent carborane group of C ₂ B ₁₀ H ₈ represented by either formula (2a) or formula (2b), and when a plurality of rings A are present in the molecule, they may be the same May be different. The organic electroluminescent element material according to claim 1, wherein the carborane compound is a carborane compound represented by the general formula (3) or (4).

Here, L ¹ , L ² , R ^{1 to} R ⁸ , p, q, and r are the same as those in the general formula (1). In General Formula (3) or (4), L ¹ and L ² are each independently a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, a substituted or unsubstituted aromatic group having 3 to 17 carbon atoms. the organic electroluminescent according to the family heterocyclic group claim 3 or an aromatic group selected from the aromatic hydrocarbon group and aromatic heterocyclic group is a 2-5 one linked to constructed linking aromatic group, Material for light emitting elements. In the general formula (3) or ^(4), independently of R 1 to R ⁶ are each, claim 3 or an aromatic hydrocarbon group having 6 to 12 aliphatic hydrocarbon group or a carbon of 1 to 10 carbon atoms 5. The material for an organic electroluminescent element according to 4 .   An organic electroluminescent device comprising an anode, an organic layer and a cathode laminated on a substrate, wherein the organic electroluminescent device comprises an organic layer containing the organic electroluminescent device material according to claim 1. Electroluminescent device. The organic electroluminescent device according to claim 6, wherein the organic layer containing the material for an organic electroluminescent device is at least one layer selected from the group consisting of a light emitting layer, an electron transport layer, and a hole blocking layer.   The organic electroluminescent element according to claim 7, wherein the organic layer containing the organic electroluminescent element material is a light emitting layer containing a phosphorescent dopant. The organic electroluminescent element according to claim 8, wherein the emission wavelength of the phosphorescent dopant has an emission maximum wavelength at 550 nm or less.

Images