Materials for organic electroluminescent devices and organic electroluminescent devices

Abstract

The present invention provides an organic EL element which has high efficiency and high driving stability, while having low driving voltage. This organic electroluminescent element is characterized by: comprising a plurality of organic layers between a positive electrode and a negative electrode; and containing a first host material, a second host material and a dopant material, each of which is selected from among indolocarbazole compounds, in a light emitting layer. The first host material is, for example, an indolocarbazole compound which has a substituent that comprises a nitrogen-containing six-membered ring such as a triazine ring; while the second host material is, for example, an indolocarbazole compound which has an aromatic hydrocarbon group or a substituent that comprises a heterocyclic ring such as a carbazole ring, a dibenzofuran ring or a dibenzothiophene ring.

Description

[Technical Field]

[0001] The present invention relates to an organic electroluminescent element comprising a compound for organic electroluminescent elements and a specific mixed host material. [Background technology]

[0002] When a voltage is applied to an organic EL element, holes are injected from the anode and electrons from the cathode into the light-emitting layer. In the light-emitting layer, the injected holes and electrons recombine to generate excitons. At this time, according to the statistical laws of electron spin, singlet excitons and triplet excitons are generated in a ratio of 1:3. Fluorescent organic EL elements that use emission from singlet excitons are said to have an internal quantum efficiency limited to 25%. On the other hand, phosphorescent organic EL elements that use emission from triplet excitons are known to be able to achieve an internal quantum efficiency of up to 100% if intersystem crossing from singlet excitons is performed efficiently.

[0003] More recently, highly efficient organic EL devices utilizing delayed fluorescence have been developed. For example, Patent Document 1 discloses an organic EL device that utilizes the TTF (Triplet-Triplet Fusion) mechanism, one of the mechanisms of delayed fluorescence. The TTF mechanism utilizes the phenomenon in which a singlet exciton is generated by the collision of two triplet excitons, and it is theoretically thought that the internal quantum efficiency can be increased to 40%. However, since its efficiency is lower compared to phosphorescent organic EL devices, further improvements in efficiency and low-voltage characteristics are required.

[0004] Furthermore, Patent Document 2 discloses an organic EL device utilizing the TADF (Thermally Activated Delayed Fluorescence) mechanism. The TADF mechanism utilizes the phenomenon in which reverse intersystem crossing occurs from triplet excitons to singlet excitons in materials where the energy difference between the singlet and triplet levels is small, and it is theoretically thought that the internal quantum efficiency can be increased to 100%.

[0005] However, in any of the mechanisms, there is room for improvement in both efficiency and lifespan. In addition, improvement is also required for reducing the driving voltage.

Prior Art Documents

Patent Documents

[0006]

Patent Document 1

Patent Document 2

Patent Document 3

Patent Document 4

Patent Document 5

Patent Document 6

Patent Document 7

[0007] Patent Documents 3, 4, and 5 disclose using indolocarbazole compounds as host materials. Patent Documents 6 and 7 disclose using two different indolocarbazole compounds as a mixed host.

[0008] However, none of them can be said to be sufficient, and further improvement in efficiency, voltage, and lifespan is desired.

Summary of the Invention

[0009] In order to apply an organic EL device to a display device such as a flat panel display, it is necessary to improve the light emission efficiency of the device and at the same time ensure sufficient long-life characteristics of the device. In view of the above situation, an object of the present invention is to provide an organic EL device having a low driving voltage, high efficiency, and high driving stability, and a compound suitable therefor.

[0010] As a result of diligent research, the inventors of the present invention have found that an organic electroluminescent device using a specific mixed host material in the light-emitting layer can solve the above problems, and have completed the present invention.

[0011] The present invention relates to an organic electroluminescent device having a plurality of organic layers between an anode and a cathode, wherein each organic layer has at least one light-emitting layer, and the light-emitting layer comprises a first host, a second host, and a dopant material that are different from each other, wherein the first host is a compound represented by the following general formula (1), and the second host is a compound represented by the following general formula (2).

[0012] [ka] Here, ring A represents an aromatic hydrocarbon ring represented by formula (1a) that is fused with two adjacent rings at arbitrary positions, and ring B represents a heterocycle represented by formula (1b) that is fused with two adjacent rings at arbitrary positions. X and Y are each independently CR 2 Or it indicates N, but at least one is N, R 1 Each of these independently represents deuterium, an aliphatic hydrocarbon group having 1 to 10 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 2 Each of these independently represents hydrogen, deuterium, an aliphatic hydrocarbon group having 1 to 10 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. a and b are integers between 0 and 4, and c is an integer between 0 and 2. Ar 1 and Ar 2 Each of these independently represents hydrogen, 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 a substituted or unsubstituted linked aromatic group in which 2 to 5 of these aromatic rings are linked together. L 1represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted linked aromatic group in which 2 to 5 of these aromatic hydrocarbon groups are linked.

[0013]

Chemical formula

[0014] In the above general formula (1), it is a preferred embodiment of the present invention that all of X, Y or both are N, L 1 is a substituted or unsubstituted phenylene group, or Ar 1 and Ar 2 are each independently hydrogen, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted linked aromatic group in which 2 to 5 of these aromatic hydrocarbon groups are linked. <000015​​​​​​​​4 In other preferred embodiments, at least one of the elements is a substituted or unsubstituted aromatic hydrocarbon group having 6 to 10 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 10 to 12 carbon atoms, or a substituted or unsubstituted linked aromatic group in which 2 to 3 of these aromatic rings are linked, or d, e, and f are all 0.

[0016] The above general formula (2) can be any of the following formulas (4a) to (4f). [ka] Here, Z is O, S, NAr 5 , or CR 5 R 6 Represents R 4 is R 3 This is equivalent to the above, where g represents an integer from 0 to 4. 3 d, e, f and Ar 3 This is equivalent to general formula (2), and Ar 5 is Ar 3 This is equivalent to R 5 and R 6 R is independent 3 This is equivalent to:

[0017] Furthermore, the present invention relates to a method for manufacturing an organic electroluminescent element, characterized in that a preliminary mixture containing the above-mentioned first and second hosts, which are different from each other, is prepared and used to produce an emissive layer. Furthermore, the present invention is a preliminary mixture for an organic electroluminescent device, characterized by comprising the above-mentioned first and second hosts, which are different from each other. It is desirable that the difference in temperature at which the first host and the second host achieve a 50% weight loss be within 20°C.

[0018] To improve device characteristics, the materials used in the organic layer must have high resistance to charge, and in particular, it is important to suppress the leakage of excitons and charge to the surrounding layers in the light-emitting layer. Improving the unevenness of the light-emitting region within the light-emitting layer is effective in suppressing this charge / exciton leakage, and to achieve this, it is necessary to control the amount of both charges (electrons / holes) injected into the light-emitting layer or the amount of both charges transported within the light-emitting layer to a desirable range. In this invention, a first host and a second host having the above-described indolocarbazole structure are used as hosts. The first host has a nitrogen-containing six-membered ring with high electron-acceptance properties on the nitrogen of the indolocarbazole, thereby improving the injection transport of charge, especially electrons. Furthermore, by using the second host, the injection transport of charge, especially holes, is enhanced, making it possible to create an organic EL element that operates stably at low voltage and high efficiency. It is also presumed that the injection transport of charge can be controlled at a high level by changing the skeletal structure of the indolocarbazole ring and the type and number of substituents on this skeletal structure. The organic EL element of this invention has optimized charge injection transport in the light-emitting layer, resulting in improved characteristics such as voltage, efficiency, and durability. [Brief explanation of the drawing]

[0019] [Figure 1] This is a schematic cross-sectional view showing an example of an organic EL element. [Modes for carrying out the invention]

[0020] The present invention relates to an organic electroluminescent device having a plurality of organic layers between an anode and a cathode, wherein each organic layer includes at least one light-emitting layer, and the light-emitting layer includes a first host represented by the general formula (1), a second host represented by the general formula (2), and a dopant material. The first host and the second host are different from each other.

[0021] In general formula (1), ring A is a benzene ring represented by formula (1a), and ring B is a heterocycle represented by formula (1b), which condenses with two adjacent rings at arbitrary positions.

[0022] The compound represented by general formula (1) can be a compound represented by the following formulas (3a) to (3f). Preferably, it is a compound represented by formulas (3a) to (3e). More preferably, it is a compound represented by formulas (3a) to (3c). Even more preferably, it is a compound represented by formula (3a). [ka]

[0023] The symbols common to general formula (1) and formulas (3a) to (3f) have the same meaning. X and Y are each independently CR 2 or N, where at least one of each is N. Preferably, two or more of X are N. More preferably, all X are N. Also preferably, two or more of Y are N. More preferably, all Y are N. Particularly preferably, all X are N and all Y are N.

[0024] R 1 and R 2 Each of these is independently hydrogen, deuterium, an aliphatic hydrocarbon group having 1 to 10 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. Preferably, it is deuterium, an aliphatic hydrocarbon group having 1 to 4 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 12 carbon atoms. More preferably, it is a substituted or unsubstituted aromatic hydrocarbon group having 6 to 10 carbon atoms, or a substituted or unsubstituted aromatic heterocyclic group having 3 to 12 carbon atoms. However, R 1 Hydrogen is excluded from this.

[0025] Specific examples of the above-mentioned aliphatic hydrocarbon groups having 1 to 10 carbon atoms include methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, and decyl. Preferably, alkyl groups having 1 to 4 carbon atoms are used.

[0026] Specific examples of the above unsubstituted aromatic hydrocarbon groups having 6 to 18 carbon atoms or unsubstituted aromatic heterocyclic groups having 3 to 17 carbon atoms include benzene, naphthalene, acenaphthene, acenaphthylene, azulene, anthracene, chrysene, pyrene, phenanthrene, fluorene, triphenylene, pyridine, pyrimidine, triazine, thiophene, isothiazole, thiazole, pyridazine, pyrrole, pyrazole, imidazole, triazole, thiadiazole, pyrazine, furan, isoxazole, quinoline, isoquinoline, quinoxaline, quinazoline, Examples of groups derived from thiadiazole, phthalazine, tetrazole, indole, benzofuran, benzothiophene, benzoxazole, benzothiazole, indazole, benzimidazole, benzotriazole, benzoisothiazole, benzothiadiazole, purine, pyranone, coumarin, isocoumarin, chromone, dibenzoselenophene, dibenzofuran, benzoflopyridine, benzoflopyrimidine, dibenzothiophene, benzothienopyridine, benzothienopyrimidine, pyridoindole, or carbazole. Preferably, aromatic groups derived from benzene, naphthalene, phenanthrene, fluorene, triphenylene, pyridine, pyrimidine, triazine, pyridazine, pyrrole, pyrazole, imidazole, triazole, pyrazine, furan, quinoline, isoquinoline, quinoxaline, quinazoline, indole, benzofuran, benzothiophene, benzoxazole, benzothiazole, indazole, benzimidazole, benzotriazole, benzoisothiazole, benzothiadiazole, dibenzoselenophene, dibenzofuran, benzoflopyridine, benzoflopyrimidine, dibenzothiophene, benzothienopyridine, benzothienopyrimidine, pyridoindole, or carbazole are included. More preferably, aromatic groups derived from benzene, naphthalene, phenanthrene, fluorene, triphenylene, triazine, quinoxaline, quinazoline, dibenzofuran, benzoflopyridine, benzoflopyrimidine, dibenzothiophene, benzothienopyridine, benzothienopyrimidine, pyridoindole, or carbazole are included.

[0027] a and b are integers between 0 and 4, and c is an integer between 0 and 2. Preferably, a and b are between 0 and 2. More preferably, a, b, and c are all 0.

[0028] Ar 1 and Ar 2 Each of these is independently a hydrogen atom, 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 a substituted or unsubstituted linked aromatic group having 2 to 5 of these aromatic rings linked together. Preferably, it is a hydrogen atom, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted linked aromatic group having 2 to 5 of the aromatic hydrocarbon groups linked together. More preferably, it is a substituted or unsubstituted phenyl group, or a substituted or unsubstituted linked aromatic group having 2 to 5 of the phenyl groups linked together.

[0029] Specific examples of the above-mentioned unsubstituted aromatic hydrocarbon groups having 6 to 18 carbon atoms, unsubstituted aromatic heterocyclic groups having 3 to 17 carbon atoms, or linked aromatic groups in which 2 to 5 of these aromatic rings are linked include benzene, naphthalene, acenaphthene, acenaphthylene, azulene, anthracene, chrysene, pyrene, phenanthrene, fluorene, triphenylene, pyridine, pyrimidine, triazine, thiophene, isothiazole, thiazole, pyridazine, pyrrole, pyrazole, imidazole, triazole, thiadiazole, pyrazine, furan, isoxazole, quinoline, isoquinoline, quinoxaline, quinazo Examples of groups derived from phosphorus, thiadiazole, phthalazine, tetrazole, indole, benzofuran, benzothiophene, benzoxazole, benzothiazole, indazole, benzimidazole, benzotriazole, benzoisothiazole, benzothiadiazole, purine, pyranone, coumarin, isocoumarin, chromone, dibenzoselenophene, dibenzofuran, benzoflopyridine, benzoflopyrimidine, dibenzothiophene, benzothienopyridine, benzothienopyrimidine, pyridoindole, carbazole, or compounds composed of 2 to 5 of these linked together. Preferably, examples of groups derived from benzene, naphthalene, phenanthrene, fluorene, triphenylene, triazine, dibenzofuran, benzoflopyridine, benzoflopyrimidine, dibenzothiophene, benzothienopyridine, benzothienopyrimidine, pyridoindole, or carbazole, or compounds composed of 2 to 5 of these linked together. More preferably, phenyl, biphenyl, or terphenyl groups. The terphenyl groups may be linked in a linear chain or branched.

[0030] In this specification, aromatic hydrocarbon groups, aromatic heterocyclic groups, or linked aromatic groups may each have substituents. Preferred substituents are deuterium, halogens, cyano groups, triarylsilyl groups, aliphatic hydrocarbon groups having 1 to 10 carbon atoms, alkenyl groups having 2 to 5 carbon atoms, alkoxy groups having 1 to 5 carbon atoms, or diarylamino groups having 12 to 44 carbon atoms. Here, if the substituent is an aliphatic hydrocarbon group having 1 to 10 carbon atoms, it may be linear, branched, or cyclic. The number of substituents is preferably 0 to 5, more preferably 0 to 2. When calculating the number of carbon atoms in aromatic hydrocarbon groups and aromatic heterocyclic groups that have substituents, the number of carbon atoms of the substituents is not included. However, it is preferable that the total number of carbon atoms including the number of carbon atoms of the substituents satisfies the above range.

[0031] Specific examples of the above substituents include deuterium, cyano, methyl, ethyl, propyl, i-propyl, butyl, t-butyl, pentyl, cyclopentyl, hexyl, cyclohexyl, heptyl, octyl, nonyl, decyl, vinyl, propenyl, butenyl, pentenyl, methoxy, ethoxy, propoxy, butoxy, pentoxy, diphenylamino, naphthylphenylamino, dinaphthylamino, dianthranylamino, diphenylenylamino, dipyrenylamino, triarylsilyl, ethenyl, propenyl, butenyl, and pentenyl. Preferably, cyano, methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, diphenylamino, naphthylphenylamino, or dinaphthylamino are used.

[0032] In this specification, a linked aromatic group refers to an aromatic group in which the carbon atoms of the aromatic ring of an aromatic group are linked by a single bond. It is an aromatic group in which two or more aromatic groups are linked together, and these may be linear or branched. The aromatic groups may be aromatic hydrocarbon groups or aromatic heterocyclic groups, and the multiple aromatic groups may be the same or different. An aromatic group that corresponds to a linked aromatic group is different from a substituted aromatic group.

[0033] L 1 This is a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted linked aromatic group in which 2 to 5 such aromatic hydrocarbon groups are linked together. Preferably, it is an aromatic hydrocarbon group having 6 to 18 carbon atoms, and more preferably, a substituted or unsubstituted phenylene group. 1 A specific example of a case where is an unsubstituted aromatic hydrocarbon group is Ar 1 and Ar 2 This is the same as when L is an unsubstituted aromatic hydrocarbon group. 1 It is a divalent group.

[0034] Specific examples of compounds represented by general formula (1) are shown below, but the list is not limited to these example compounds.

[0035] [ka] [ka] [ka]

[0036] [ka] [ka] [ka]

[0037] [ka] [ka] [ka]

[0038] [ka] [ka] [ka]

[0039] [ka]

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[0040]

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[0041]

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[0042]

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[0043]

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[0044]

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[0045] [ka] [ka] [ka]

[0046] [ka] [ka] [ka]

[0047] [ka] [ka] [ka]

[0048] In the general formula (2) above, ring C represents a benzene ring represented by formula (2a), and ring D represents a heterocycle represented by formula (2b), which is fused with two adjacent rings at arbitrary positions.

[0049] Ar 3 , and Ar 4Each of these independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 18 carbon atoms, or a substituted or unsubstituted linked aromatic group having 2 to 5 of these aromatic rings linked together. As the aromatic heterocyclic group, a substituted or unsubstituted aromatic heterocyclic group having 10 to 18 carbon atoms is preferred, and as the linked aromatic group, a substituted or unsubstituted linked aromatic group having 2 to 3 of the above aromatic groups linked together is preferred.

[0050] Ar 3 , and Ar 4 It is even more preferable that at least one of them is a substituted or unsubstituted aromatic heterocyclic group having 10 to 12 carbon atoms. Also, Ar 3 and Ar 4 Preferably, it does not have a nitrogen-containing 6-membered ring group. More preferably, Ar 3 It is not a nitrogen-containing 6-membered ring group, Ar 4 If the first aromatic group is a linked aromatic group, then the second aromatic group is not a nitrogen-containing six-membered ring group.

[0051] The compound represented by general formula (2) can be the compound represented by formulas (4a) to (4f) above. Preferably, it is the compound represented by formulas (4a) to (4e). More preferably, it is the compound represented by formulas (4a) to (4c).

[0052] The symbols common to general formula (2) and formulas (4a) to (4f) have the same meaning. In equations (4a) to (4f), Z is O, S, NAr. 5 , or CR 5 R 6 It represents, preferably S, O, or N-Ar 5 It is, more preferably O, or N-Ar 5 That is the case.

[0053] Ar 5 The above Ar 1 Or Ar 2The same applies. Preferably, it is a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted linked aromatic group in which 2 to 3 such aromatic hydrocarbon groups are linked together, and more preferably, it is an unsubstituted aromatic hydrocarbon group having 6 to 12 carbon atoms, or a substituted or unsubstituted linked aromatic group in which 2 to 3 such aromatic hydrocarbon groups are linked together.

[0054] Specific examples of the above-mentioned unsubstituted aromatic hydrocarbon groups having 6 to 18 carbon atoms, unsubstituted aromatic heterocyclic groups having 3 to 18 carbon atoms, or linked aromatic groups in which 2 to 5 of these aromatic rings are linked include benzene, naphthalene, acenaphthene, acenaphthylene, azulene, anthracene, chrysene, pyrene, phenanthrene, fluorene, triphenylene, pyridine, pyrimidine, triazine, thiophene, isothiazole, thiazole, pyridazine, pyrrole, pyrazole, imidazole, triazole, thiadiazole, pyrazine, furan, isoxazole, quinoline, isoquinoline, quinoxaline, quinazoline, thiadiazole, phthalazine, and tetrazole. Examples include indole, benzofuran, benzothiophene, benzoxazole, benzothiazole, indazole, benzimidazole, benzotriazole, benzoisothiazole, benzothiadiazole, purine, pyranone, coumarin, isocoumarin, chromone, dibenzoselenophene, dibenzofuran, benzoflopyridine, benzoflopyrimidine, dibenzothiophene, benzothienopyridine, benzothienopyrimidine, carbazole, pyridoindole, indolocarbazole, benzoflocarbazole, benzothienocarbazole, or groups obtained by removing one hydrogen atom from compounds composed of 2 to 5 of these linked together. Preferably, the groups are those obtained by removing one hydrogen atom from benzene, naphthalene, phenanthrene, fluorene, triphenylene, dibenzofuran, benzoflopyridine, benzoflopyrimidine, dibenzothiophene, benzothienopyridine, benzothienopyrimidine, carbazole, pyridoindole, indolocarbazole, benzoflocarbazole, benzothienocarbazole, or compounds composed of 2 to 3 of these linked together. More preferably, the groups are those obtained by removing one hydrogen atom from benzene, dibenzofuran, dibenzothiophene, carbazole, or compounds composed of 2 to 3 of these linked together.

[0055] R 3 , and R 4Each of these is independently a deuterium, an aliphatic hydrocarbon group having 1 to 10 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. Preferably, it is a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, and more preferably, it is a substituted or unsubstituted aromatic hydrocarbon group having 6 to 12 carbon atoms.

[0056] R 5 , and R 6 Each of these is independently hydrogen, an aliphatic carbonized water group having 1 to 10 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, and these may be bonded to each other to form a ring.

[0057] R 3 ~R 6 A specific example of a case where is an unsubstituted aliphatic hydrocarbon group, an aromatic hydrocarbon group, or an aromatic heterocyclic group is R 1 and R 2 The same applies as in the previous case. Preferably, the following are benzene, naphthalene, acenaphthene, acenaphthylene, azulene, anthracene, chrysene, pyrene, phenanthrene, fluorene, or triphenylene. More preferably, benzene.

[0058] d, e, and g are integers between 0 and 4, and f is an integer between 0 and 2. Preferably, d, e, and g are integers between 0 and 2, and f is an integer between 0 and 1. More preferably, d, e, f, and g are all 0.

[0059] Specific examples of compounds represented by general formula (2) are shown below, but the examples are not limited to these.

[0060] [ka] TIFF0007842694000045.tif40165 [ka] [ka]

[0061] [ka] [ka] [ka] TIFF0007842694000051.tif52170 [ka]

[0062] The organic electroluminescent device of the present invention has an organic layer, and at least one of the organic layers is a light-emitting layer. At least one light-emitting layer contains the first host, the second host, and at least one type of light-emitting dopant.

[0063] A preferred method for manufacturing the organic electroluminescent element of the present invention involves preparing a preliminary mixture (pre-mixed composition) containing the first host and the second host, and using this mixture to produce a light-emitting layer. A method of vaporizing the preliminary mixture from a single evaporation source and depositing it is preferred. Here, the preliminary mixture is preferably a homogeneous composition. Ensuring that the difference in the 50% weight loss temperature between the first and second hosts in the premix is ​​within 20°C is effective in ensuring uniform deposition.

[0064] The first and second hosts can be deposited individually from different deposition sources, but it is preferable to pre-mix them to form a premixture before deposition and then simultaneously deposit this premixture from a single deposition source to form the light-emitting layer. In this case, the premixture may contain the light-emitting dopant material necessary for forming the light-emitting layer or other hosts used as needed, but if there is a large difference in the temperature at which the desired vapor pressure is reached, it is preferable to deposit them from different deposition sources.

[0065] Furthermore, the mixing ratio (weight ratio) of the first host and the second host is preferably such that the proportion of the first host is 10-70% of the total of the first and second hosts, more preferably more than 15% and less than 65%, and more preferably 20-60%.

[0066] Next, the structure of the organic EL element of the present invention will be described with reference to the drawings, but the structure of the organic EL element of the present invention is not limited thereto.

[0067] Figure 1 is a cross-sectional view showing an example of the structure of a typical organic EL element used in the present invention, where 1 is the substrate, 2 is the anode, 3 is the hole injection layer, 4 is the hole transport layer, 5 is the light-emitting layer, 6 is the electron transport layer, and 7 is the cathode. The organic EL element of the present invention may have an exciton blocking layer adjacent to the light-emitting layer, or an electron blocking layer between the light-emitting layer and the hole injection layer. The exciton blocking layer can be inserted on either the cathode side or the anode side of the light-emitting layer, and it is also possible to insert both simultaneously. The organic EL element of the present invention has an anode, a light-emitting layer, and a cathode as essential layers, but it is also common to have a hole injection transport layer and an electron injection transport layer in addition to the essential layers, and it is also common to have a hole blocking layer between the light-emitting layer and the electron injection transport layer. Note that the hole injection transport layer means either the hole injection layer or the hole transport layer, or both, and the electron injection transport layer means either the electron injection layer or the electron transport layer, or both.

[0068] It is also possible to stack the cathode 7, electron transport layer 6, light-emitting layer 5, hole transport layer 4, and anode 2 on the substrate 1 in the reverse order of Figure 1, and in this case as well, layers can be added or omitted as needed.

[0069] -substrate- The organic EL element of the present invention is preferably supported on a substrate. There are no particular restrictions on this substrate; any substrate that has been conventionally used in organic EL elements is acceptable, such as those made of glass, transparent plastic, or quartz.

[0070] -anode- For the anode material in an organic EL device, materials consisting of metals, alloys, electrically conductive compounds, or mixtures thereof with a large work function (4 eV or more) are preferably used. Specific examples of such electrode materials include metals such as Au, and conductive transparent materials such as CuI, indium tin oxide (ITO), SnO2, and ZnO. Amorphous materials such as IDIXO (In2O3-ZnO), which can be used to create transparent conductive films, may also be used. The anode may be formed by creating a thin film from these electrode materials by methods such as vapor deposition or sputtering, and then forming a pattern of the desired shape using photolithography. Alternatively, if high pattern accuracy is not required (around 100 μm or more), the pattern may be formed via a mask of the desired shape during vapor deposition or sputtering of the electrode material. When using a coatable substance such as an organic conductive compound, wet film formation methods such as printing or coating can also be used. When extracting light from this anode, it is desirable to have a transmittance greater than 10%, and the sheet resistance of the anode is preferably several hundred Ω / □ or less. The film thickness depends on the material, but is usually selected within the range of 10 to 1000 nm, preferably 10 to 200 nm.

[0071] -cathode- On the other hand, materials consisting of metals (electron-injection metals), alloys, electrically conductive compounds, or mixtures thereof with a small work function (4 eV or less) are used as cathode materials. Specific examples of such electrode materials include sodium, sodium-potassium alloys, magnesium, lithium, magnesium / copper mixtures, magnesium / silver mixtures, magnesium / aluminum mixtures, magnesium / indium mixtures, aluminum / aluminum oxide (Al2O3) mixtures, indium, lithium / aluminum mixtures, and rare earth metals. Among these, from the viewpoint of electron injection and durability against oxidation, mixtures of electron-injection metals and metalloids with a larger and more stable work function, such as magnesium / silver mixtures, magnesium / aluminum mixtures, magnesium / indium mixtures, aluminum / aluminum oxide mixtures, lithium / aluminum mixtures, and aluminum, are preferred. Cathodes can be fabricated by forming thin films of these cathode materials by methods such as vapor deposition or sputtering. Furthermore, the sheet resistance of 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. Furthermore, to allow the emitted light to pass through, it is advantageous if either the anode or cathode of the organic EL element is transparent or semi-transparent, as this improves the luminescence brightness.

[0072] Furthermore, by forming the above-mentioned metal with a film thickness of 1 to 20 nm and then forming the conductive transparent material mentioned in the description of the anode on top of it, a transparent or translucent cathode can be fabricated. By applying this, it is possible to fabricate an element in which both the anode and cathode are transparent.

[0073] —Emitting layer— The light-emitting layer is a layer that emits light after excitons are generated by the recombination of holes and electrons injected from the anode and cathode, respectively. The light-emitting layer contains an organic light-emitting dopant material and a host.

[0074] The hosts used are the first and second hosts, which are different from each other. The compound represented by general formula (1) as the first host may be one compound or two or more different compounds. Similarly, the compound represented by general formula (2) as the second host, which is different from the first host, may be one compound or two or more different compounds. If necessary, one or more other known host materials may be used in combination, but the amount used should be 50 wt% or less, preferably 25 wt% or less, of the total host material.

[0075] The host and its premixture may be in the form of a powder, stick, or granules.

[0076] When using multiple types of hosts, each host can be deposited from a different deposition source, or multiple types of hosts can be deposited simultaneously from a single deposition source by pre-mixing them into a premixture before deposition.

[0077] For pre-mixing, a method that allows for as uniform a mixture as possible is desirable. Examples include grinding and mixing, heating and melting under reduced pressure or inert gas atmosphere such as nitrogen, and sublimation, but the method is not limited to these.

[0078] When using a pre-mixed first and second host, in order to reproducibly fabricate organic EL elements with good characteristics, the 50% weight loss temperature (T) is used. 50 A small difference in weight is desirable. The 50% weight loss temperature is the temperature at which the weight decreases by 50% when the temperature is raised from room temperature to 550°C at a rate of 10°C per minute in TG-DTA measurements under reduced pressure with a nitrogen flow (1 Pa). Around this temperature, vaporization by evaporation or sublimation is thought to occur most actively.

[0079] Preferably, the difference in the 50% weight loss temperature between the first host and the second host is within 20°C, and more preferably within 15°C. As a pre-mixing method, known methods such as grinding and mixing can be used, but it is desirable to mix as uniformly as possible.

[0080] When using phosphorescent dopants as luminescent dopant materials, the phosphorescent dopant should preferably contain an organometallic complex comprising at least one metal selected from ruthenium, rhodium, palladium, silver, rhenium, osmium, iridium, platinum, and gold. Specifically, iridium complexes described in J.Am.Chem.Soc.2001,123,4304 and JP 2013-530515 are preferably used, but are not limited to these.

[0081] The phosphorescent dopant material may be contained in the luminescent layer by one type or by two or more types. The content of the phosphorescent dopant material is preferably 0.1 to 30 wt%, and more preferably 1 to 20 wt%, relative to the host material.

[0082] Phosphorescent dopant materials are not particularly limited, but specific examples include the following:

[0083] [ka] [ka]

[0084] When using a fluorescent dopant as a luminescent dopant material, the fluorescent dopant is not particularly limited, but examples include 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, pyrrolidine derivatives, cyclopentadiene derivatives, bisstyrylanthracene derivatives, quinacridone derivatives, pyrrolopyridine derivatives, thiadiazolopyridine derivatives, styrylamine derivatives, diketopyrrolopyrrole derivatives, aromatic dimethylidine compounds, metal complexes of 8-quinolinol derivatives and pyromethene derivatives, various metal complexes represented by rare earth complexes and transition metal complexes, polymer compounds such as polythiophene, polyphenylene, and polyphenylene vinylene, and organosilane derivatives. Preferably, these include condensed aromatic derivatives, styryl derivatives, diketopyrrolopyrrole derivatives, oxazine derivatives, pyromethene metal complexes, transition metal complexes, or lanthanide complexes. More preferably, these include naphthalene, pyrene, chrysene, triphenylene, benzo[c]phenanthrene, benzo[a]anthracene, pentacene, perylene, fluorantene, acenaphsofluorantene, dibenzo[a,j]anthracene, dibenzo[a,h]anthracene, benzo[a]naphthalene, hexacene, naphtho[2,1-f]isoquinoline, α-naphthaphenanthidine, phenanthroxazole, quinolino[6,5-f]quinoline, benzothiophanthrene, and the like. These may have alkyl groups, aryl groups, aromatic heterocyclic groups, or diarylamino groups as substituents.

[0085] The fluorescent dopant material may be present in the light-emitting layer in a single type or in two or more types. The content of the fluorescent dopant material is preferably 0.1 to 20% relative to the host material, and more preferably 1 to 10%.

[0086] When using a thermally activated delayed fluorescence dopant as a luminescent dopant material, examples of thermally activated delayed fluorescence dopants are not particularly limited, but include metal complexes such as tin complexes and copper complexes, indolocarbazole derivatives described in WO2011 / 070963, cyanobenzene derivatives and carbazole derivatives described in Nature 2012,492,234, phenazine derivatives, oxadiazole derivatives, triazole derivatives, sulfone derivatives, phenoxazine derivatives, and acridine derivatives described in Nature Photonics 2014,8,326.

[0087] Thermally activated delayed fluorescence dopant materials are not particularly limited, but specific examples include the following:

[0088] [ka]

[0089] The thermally activated delayed fluorescence dopant material may be contained in the luminescence layer as a single type or as two or more types. Furthermore, the thermally activated delayed fluorescence dopant may be used in mixture with phosphorescent dopants or fluorescent dopants. The content of the thermally activated delayed fluorescence dopant material is preferably 0.1 to 50% of the host material, and more preferably 1 to 30%.

[0090] -Injection layer- An injection layer is a layer provided between the electrode and the organic layer to reduce the driving voltage and improve the luminescence brightness. There are hole injection layers and electron injection layers, and they may be present between the anode and the light-emitting layer or hole transport layer, and between the cathode and the light-emitting layer or electron transport layer. The injection layer can be provided as needed.

[0091] -Hole blocking layer- In a broad sense, a hole blocking layer functions as an electron transport layer. It consists of a hole blocking material that has the ability to transport electrons but significantly less ability to transport holes. By blocking holes while transporting electrons, it is possible to improve the probability of electron-hole recombination in the light-emitting layer.

[0092] -Electron blocking layer- In a broad sense, an electron blocking layer functions as a hole transport layer, and by blocking electrons while transporting holes, it can improve the probability of electrons and holes recombining in the light-emitting layer.

[0093] As the material for the electron blocking layer, known electron blocking layer materials can be used, and the material for the hole transport layer described later can be used as needed. The thickness of the electron blocking layer is preferably 3 to 100 nm, and more preferably 5 to 30 nm.

[0094] -Exciton blocking layer- An exciton blocking layer is a layer designed to prevent excitons, generated by the recombination of holes and electrons within the light-emitting layer, from diffusing into the charge transport layer. By inserting this layer, excitons can be efficiently confined within the light-emitting layer, thereby improving the light-emitting efficiency of the device. In devices where two or more light-emitting layers are adjacent, the exciton blocking layer can be inserted between two adjacent light-emitting layers.

[0095] As the material for the exciton blocking layer, known exciton blocking layer materials can be used. Examples include 1,3-dicarbazolylbenzene (mCP) and bis(8-hydroxy-2-methylquinoline)-(4-phenylphenoxy)aluminum(III)(BAlq).

[0096] - Hole transport layer - A hole transport layer consists of a hole transport material that has the function of transporting holes, and the hole transport layer can be a single layer or multiple layers.

[0097] The hole transport material has either hole injection or transport properties, or electron barrier properties, and may be either organic or inorganic. Any compound from conventionally known compounds can be selected and used for the hole transport layer. Examples of such hole transport materials include porphyrin derivatives, arylamine derivatives, triazole derivatives, oxadiazole derivatives, imidazole derivatives, polyarylalkane derivatives, pyrazoline derivatives and pyrazolone derivatives, phenylenediamine derivatives, arylamine derivatives, aminosubstituted chalcone derivatives, oxazole derivatives, styrylanthracene derivatives, fluorenone derivatives, hydrazone derivatives, stilbene derivatives, silazane derivatives, aniline copolymers, and conductive polymer oligomers, particularly thiophene oligomers. However, it is preferable to use porphyrin derivatives, arylamine derivatives and styrylamine derivatives, and more preferably arylamine compounds.

[0098] -Electron transport layer- An electron transport layer consists of a material that has the function of transporting electrons, and the electron transport layer can consist of a single layer or multiple layers.

[0099] The electron transport material (which may also serve as a hole-blocking material) only needs to have the function of transferring electrons injected from the cathode to the light-emitting layer. Any compound from conventionally known compounds can be selected and used for the electron transport layer. Examples include polycyclic aromatic derivatives such as naphthalene, anthracene, and phenanthroline; tris(8-hydroxyquinoline)aluminum(III) derivatives; phosphine oxide derivatives; nitro-substituted fluorene derivatives; diphenylquinone derivatives; thiopyrandioxide derivatives; carbodiimide; phreolenylidenemethane derivatives; anthraquinodimethane and anthrone derivatives; bipyridine derivatives; quinoline derivatives; oxadiazole derivatives; benzimidazole derivatives; benzothiazole derivatives; indolocarbazole derivatives; and polymer materials that incorporate these materials into a polymer chain or use these materials as the main chain of the polymer. [Examples]

[0100] The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these examples and can be implemented in various forms as long as it does not exceed the gist of the invention.

[0101] Example 1 Each thin film is deposited on a glass substrate with an anode made of ITO with a thickness of 110 nm using vacuum deposition at a vacuum level of 4.0 × 10⁻⁶. -5 The layers were stacked using Pa. First, a 25nm thick layer of HAT-CN was formed on ITO as a hole injection layer, followed by a 30nm thick layer of Spiro-TPD as a hole transport layer. Next, a 10nm thick layer of HT-1 was formed as an electron blocking layer. Then, compound 1 was co-deposited as the first host, compound 649 as the second host, and Ir(ppy)3 as the light-emitting dopant from different deposition sources to form a 40nm thick light-emitting layer. At this time, the co-deposit conditions were such that the concentration of Ir(ppy)3 was 10wt% and the weight ratio of the first host to the second host was 30:70. Next, an ET-1 layer was formed as an electron transport layer to a thickness of 20nm. Furthermore, a 1nm thick layer of LiF was formed on the electron transport layer as an electron injection layer. Finally, an Al layer was formed on the electron injection layer to a thickness of 70nm as a cathode to fabricate an organic EL device.

[0102] Examples 2-7 In Example 1, an organic EL element was fabricated in the same manner as in Example 1, except that the first and second hosts were compounds shown in Table 1. The weight ratio of the first host to the second host was 30:70 in Examples 2 to 6, and 50:50 in Example 7.

[0103] Examples 8-10 An organic EL element was fabricated in the same manner as in Example 1, except that the preliminary mixture obtained by weighing out the first host and the second host shown in Table 1 and grinding them in a mortar was co-deposited from a single deposition source. The weight ratio of the first host to the second host was 30:70 in Examples 8 and 9, and 50:50 in Example 10.

[0104] Comparative Examples 1-5 In Example 1, an organic EL element was fabricated in the same manner as in Example 1, except that the first and second hosts were compounds shown in Table 1.

[0105] Comparative Example 6 In Example 8, an organic EL element was fabricated in the same manner as in Example 8, except that the first and second hosts were compounds shown in Table 1.

[0106] Comparative Example 7 In Example 10, an organic EL element was fabricated in the same manner as in Example 10, except that the first and second hosts were compounds shown in Table 1.

[0107] Table 1 shows the evaluation results of the fabricated organic EL elements. In the table, brightness, drive voltage, and luminous efficiency are calculated using a drive current of 20 mA / cm². 2 This value represents the initial characteristics. LT70 is the time it takes for the initial brightness to decay to 70%, and it represents the lifetime characteristics.

[0108] [Table 1]

[0109] The results in Table 1 show that Examples 1-10 exhibit improved power efficiency or lifespan compared to the comparative examples, demonstrating superior characteristics.

[0110] The compounds used in the examples are listed below. [ka]

[0111] Table 2 shows the 50% weight loss temperature (T 50 ) is written. [Table 2]

Claims

1. An organic electroluminescent element having a plurality of organic layers between an anode and a cathode, wherein each organic layer has at least one light-emitting layer, the light-emitting layer comprises a first host, a second host and a dopant material that are different from each other, the first host being a compound represented by any of the following formulas (3a) to (3e), and the second host being a compound represented by the following general formula (2). 【Chemistry 1】 Here, X and Y are all N, R １ Each of these independently represents deuterium, an aliphatic hydrocarbon group having 1 to 10 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 ２ Each of these independently represents hydrogen, deuterium, an aliphatic hydrocarbon group having 1 to 10 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. a and b are integers between 0 and 4, and c is an integer between 0 and 2. Ar １ and Ar ２ Each of these independently represents hydrogen, 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 a substituted or unsubstituted linked aromatic group in which 2 to 5 of these aromatic rings are linked together. L １ This refers to a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted linked aromatic group in which 2 to 5 such aromatic hydrocarbon groups are linked together. 【Chemistry 2】 Here, ring C represents an aromatic hydrocarbon ring represented by formula (2a) that is fused with two adjacent rings at arbitrary positions, and ring D represents a heterocycle represented by formula (2b) that is fused with two adjacent rings at arbitrary positions. R ３ Each of these independently represents deuterium, an aliphatic hydrocarbon group having 1 to 10 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. d and e are integers from 0 to 4, and f is an integer from 0 to 2. Ar ３ , and Ar ４ Each of these independently represents a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 18 carbon atoms, or a substituted or unsubstituted linked aromatic group in which 2 to 5 of these aromatic rings are linked together.

2. In the above formulas (3a) to (3e), L １ The organic electroluminescent device according to claim 1, wherein is a substituted or unsubstituted phenylene group.

3. In the above formulas (3a) to (3e), Ar １ and Ar ２ The organic electroluminescent element according to claim 1 or 2, characterized in that each of them is independently hydrogen, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted linked aromatic group in which 2 to 5 aromatic hydrocarbon groups are linked together.

4. In the above general formula (2), Ar ３ , and Ar ４ The organic electroluminescent element according to any one of claims 1 to 3, wherein each is independently a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 10 to 18 carbon atoms, or a substituted or unsubstituted linked aromatic group in which 2 to 5 of these aromatic rings are linked together.

5. In the above general formula (2), Ar ３ , and Ar ４ The organic electroluminescent element according to any one of claims 1 to 4, wherein at least one of the elements is a substituted or unsubstituted aromatic hydrocarbon group having 6 to 10 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 10 to 12 carbon atoms, or a substituted or unsubstituted linked aromatic group in which two to three of these aromatic rings are linked together.

6. The organic electroluminescent element according to any one of claims 1 to 5, characterized in that, in the above general formula (2), d, e, and f are all 0.

7. The organic electroluminescent element according to any one of claims 1 to 6, wherein the above general formula (2) is any of the following formulas (4a) to (4f). 【Transformation 3】 Here, Z is O, S, NAr ５ , or CR ５ R ６ Represents R ４ is R ３ This is equivalent to the above, where g represents an integer from 0 to 4. ３ d, e, f and Ar ３ This is synonymous with general formula (2), and Ar ５ Ar ３ This is equivalent to R ５ and R ６ R is independent ３ This is equivalent to:

8. A method for manufacturing an organic electroluminescent element according to any one of claims 1 to 7, characterized by preparing a premixed composition containing the above-mentioned different first and second hosts, and using it to produce an emissive layer.

9. A premixed composition for use in a method for manufacturing an organic electroluminescent element according to claim 8, characterized in that it comprises the above-mentioned first and second hosts which are different from each other.

10. The premixed composition according to claim 9, characterized in that the difference in the 50% weight loss temperature between the first host and the second host is within 20°C.

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