JP2007194504A - Organic electroluminescence element - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a durable organic electroluminescence element having high luminous efficiency, and to provide a suitable aromatic ring compound used for the organic electroluminescence element. <P>SOLUTION: By containing a ring compound in a specific structure in at least one type of organic compound layer, the durable organic electroluminescence element having high luminous efficiency (for example, external quantum efficiency) is obtained. Also, by using the compound having a specific structure, a durable element can be manufactured that emits light with high external quantum efficiency in a blue region. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention relates to an organic electroluminescence device that emits light by converting electric energy into light.

  Organic electroluminescent elements (hereinafter also referred to as “organic EL elements”) are actively researched and developed because they can emit light with high luminance when driven at a low voltage. An organic electroluminescent element has an organic compound layer between a pair of electrodes, and electrons injected from the cathode and holes injected from the anode are recombined in the organic compound layer to emit the energy of the generated excitons. It is used for.

  In recent years, the use of phosphorescent materials has increased the efficiency of devices, and inventions relating to phosphorescent devices using iridium complexes or platinum complexes as phosphorescent materials have been disclosed (for example, Patent Document 1 and Patent Document 1). 2). However, an element that achieves both high efficiency and high durability has not been developed yet.

In addition, an invention relating to an organic EL element that uses a material that combines only a stable six-membered aromatic ring with a view to a highly durable material is disclosed (for example, see Patent Document 3). However, the materials used for these materials have a low condensed triplet level (T ₁ level) of the molecule, such as a condensed ring or a long conjugated system. Therefore, when used in a phosphorescent light emitting element, the light emission efficiency is lowered because the light emission of the phosphorescent material is quenched. This is conspicuous when light is emitted at a shorter wavelength, and when used in a blue phosphorescent element, the light emission is greatly quenched.
US Pat. No. 6,303,238 International Publication No. 00/57676 Pamphlet JP 2002-356449 A

  An object of the present invention is to provide an organic electroluminescent device having high luminous efficiency and high durability. Moreover, it exists in provision of the aromatic cyclic compound suitable for using for it.

  As a result of studies to solve the above problems, the present inventors have found that an organic EL element containing a cyclic compound having a specific structure in an organic compound layer solves the above problems. That is, the present invention has been achieved by the following means.

  [1] An organic electroluminescent device having at least one organic compound layer including a light emitting layer containing a light emitting material between a pair of electrodes, wherein at least one compound represented by the following general formula (I) is organic An organic electroluminescent device comprising a compound layer.

(In the general formula (I), Ar ^{1 to} Ar ⁵ represent an aromatic hydrocarbon ring or an aromatic heterocycle. Q represents an atomic group necessary for forming an aromatic hydrocarbon ring or an aromatic heterocycle. .)

  [2] The organic electroluminescence device as described in [1] above, wherein the compound represented by the general formula (I) is represented by the following general formula (II).

(In the general formula (II), Ar ²¹ and Ar ²² represent an aromatic hydrocarbon ring or an aromatic heterocycle. A ^{1 to} A ¹⁶ represent C—R ²¹ or N. R ²¹ represents a hydrogen atom or a substituent. A plurality of R ²¹ may be the same or different.)

  [3] The organic electroluminescent element as described in [2] above, wherein the compound represented by the general formula (I) is represented by the following general formula (III).

(In general formula (III), Ar ³¹ and Ar ³² represent an aromatic hydrocarbon ring or an aromatic heterocycle. R ^{1 to} R ¹⁶ represent a hydrogen atom or a substituent.)

  [4] The organic electroluminescent element as described in [3] above, wherein the compound represented by (III) is represented by the following general formula (IV).

(In general formula (IV), R ^{1 to} R ²⁰ represent a hydrogen atom or a substituent. X ^{1 to} X ⁴ represent an N atom or C—R ⁴¹ , and R ⁴¹ represents a hydrogen atom or a substituent.)

  [5] The organic electroluminescent element as described in [3] above, wherein the compound represented by the general formula (III) is represented by the following general formula (V).

(In general formula (V), R ^{1 to} R ¹⁶ and R ^{21 to} R ²⁴ represent a hydrogen atom or a substituent. X ^{5 to} X ⁸ represent an N atom or C—R ⁵¹ , and R ⁵¹ represents a hydrogen atom or Represents a substituent.)

  [6] The glass transition temperature of the compound represented by the general formulas (I) to (V) is 130 ° C. or higher and 450 ° C. or lower, according to any one of the above [1] to [5] Organic electroluminescent device.

  [7] The lowest excited triplet energy level of the compounds represented by the general formulas (I) to (V) is 65 kcal / mol (272.35 kJ / mol) or more and 95 kcal / mol (398.05 kJ / mol) or less. The organic electroluminescent element as described in any one of [1] to [6] above, wherein

  [8] The organic electroluminescent element as described in any one of [1] to [7] above, wherein at least one of the light emitting materials is a phosphorescent light emitting material.

[9] The organic electroluminescence device as described in [8] above, wherein the phosphorescent material is an iridium complex or a platinum complex.
[10] The organic electroluminescent element as described in any one of [1] to [9] above, wherein the compound represented by the general formulas (I) to (V) is contained in the light emitting layer.

  In the organic electroluminescent device of the present invention, at least one organic compound layer containing a cyclic compound represented by the general formulas (I) to (V) of the present invention (used in the present specification in the same meaning as the “compound of the present invention”). It is contained in. Thereby, an organic electroluminescent element (used in the present specification and synonymous with “the element of the present invention”) having high luminous efficiency (for example, external quantum efficiency) and excellent durability can be provided. In addition, by using the compound of the present invention having a specific structure, it is possible to provide an element that emits light with high external quantum efficiency in the blue region and is excellent in durability.

  The organic electroluminescent element of the present invention has at least one organic light emitting layer (light emitting layer) as an organic compound layer. As the organic compound layer other than the light emitting layer, a hole injection layer, a hole transport layer, an electron block layer, an exciton block layer, a hole block layer, an electron transport layer, an electron injection layer, a protective layer, and the like are appropriately disposed. They may also have the functions of other layers. Each layer may be composed of a plurality of layers.

  The organic electroluminescent element of the present invention may use light emitted from excited singlet (fluorescence) or light emitted from excited triplet (phosphorescence), but uses phosphorescence from the viewpoint of light emission efficiency. The one is preferred.

  When the organic electroluminescent element of the present invention uses phosphorescence, the light emitting layer is preferably composed of at least one phosphorescent material and at least one host material. Here, the host material is a material other than the light emitting material among the materials constituting the light emitting layer, and functions to disperse the light emitting material and hold it in the layer, and receive holes from the anode, the hole transport layer, and the like. Function, function to receive electrons from cathode, electron transport layer, etc., function to transport holes and / or electrons, function to provide recombination field of holes and electrons, and emit energy of excitons generated by recombination It means a material having at least one of a function of transferring to a material and a function of transporting holes and / or electrons to a light emitting material.

  The compound of the present invention may be contained in any one of the organic compound layers, and may be contained in a plurality of layers, but the light emitting layer, the hole blocking layer, the electron transport layer, the electron injection layer And is most preferably contained as a host material in the light emitting layer. When contained in the light emitting layer as a host material, the content of the compound of the present invention in the light emitting layer is preferably 50 to 99.9% by mass, and more preferably 60 to 99% by mass. Moreover, when it contains in a hole block layer, an electron carrying layer, and an electron injection layer, it is preferable that the content rate of the compound of this invention in each layer is 70-100 mass%, and it is 85-100 mass%. More preferred is 100% by mass.

  The compound represented by formula (I) of the present invention will be described in detail.

(In the general formula (I), Ar ^{1 to} Ar ⁵ represent an aromatic hydrocarbon ring or an aromatic heterocycle. Q represents an atomic group necessary for forming an aromatic hydrocarbon ring or an aromatic heterocycle. .)

Although it does not specifically limit as an aromatic hydrocarbon ring or aromatic heterocycle represented by Ar < ¹ > -Ar < ⁵ >, 4-10 membered ring is preferable, 5-7 membered ring is more preferable, and 5 and 6 membered ring are further A 6-membered ring is preferable. The heteroatom contained in the aromatic heterocycle represented by Ar ^{1 to} Ar ⁵ is not particularly limited, but an aromatic heterocycle containing nitrogen, oxygen, sulfur, selenium, silicon, germanium, or phosphorus is preferable, and nitrogen, oxygen, Sulfur is more preferable, nitrogen and oxygen are more preferable, and nitrogen is particularly preferable. The number of heteroatoms contained in one aromatic heterocycle represented by Ar ^{1 to} Ar ⁵ is not particularly limited, but is preferably 1 to 3.

Specific examples of the aromatic hydrocarbon ring or aromatic heterocycle represented by Ar ^{1 to} Ar ⁵ include benzene ring, pyridine ring, pyrazine ring, pyrimidine ring, pyridazine ring, triazine ring, pyrrole ring, pyrazole ring, imidazole. Examples include a ring, a triazole ring, an oxazole ring, an oxadiazole ring, a thiazole ring, a thiadiazole ring, a furan ring, a thiophene ring, a selenophene ring, a silole ring, a gelmol ring, and a phosphole ring.
The aromatic hydrocarbon ring or aromatic heterocycle represented by Ar ^{1 to} Ar ⁵ may have a substituent, and as the substituent, those listed as the following substituent group A can be applied.

(Substituent group A)
An alkyl group (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 10 carbon atoms, such as methyl, ethyl, iso-propyl, tert-butyl, n-octyl, n- Decyl, n-hexadecyl, cyclopropyl, cyclopentyl, cyclohexyl, etc.), an alkenyl group (preferably having 2 to 30 carbon atoms, more preferably 2 to 20 carbon atoms, particularly preferably 2 to 10 carbon atoms, For example, vinyl, allyl, 2-butenyl, 3-pentenyl, etc.), alkynyl group (preferably having 2 to 30 carbon atoms, more preferably 2 to 20 carbon atoms, particularly preferably 2 to 10 carbon atoms, For example, propargyl, 3-pentynyl, etc.), aryl groups (preferably having 6 to 30 carbon atoms, more preferably A prime number of 6 to 20, particularly preferably a carbon number of 6 to 12, such as phenyl, p-methylphenyl, naphthyl, anthranyl, etc., an amino group (preferably a carbon number of 0 to 30, more preferably a carbon number). 0 to 20, particularly preferably 0 to 10 carbon atoms, such as amino, methylamino, dimethylamino, diethylamino, dibenzylamino, diphenylamino, ditolylamino, etc.), an alkoxy group (preferably 1 to 1 carbon atoms). 30, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 10 carbon atoms, and examples thereof include methoxy, ethoxy, butoxy, 2-ethylhexyloxy and the like, and aryloxy groups (preferably 6 carbon atoms). -30, more preferably 6-20 carbons, particularly preferably 6-12 carbons, Phenyloxy, 1-naphthyloxy, 2-naphthyloxy, etc.), a heterocyclic oxy group (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, and particularly preferably 1 to 12 carbon atoms). For example, pyridyloxy, pyrazyloxy, pyrimidyloxy, quinolyloxy, etc.), acyl group (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 12 carbon atoms, Acetyl, benzoyl, formyl, pivaloyl, etc.), an alkoxycarbonyl group (preferably having 2 to 30 carbon atoms, more preferably 2 to 20 carbon atoms, particularly preferably 2 to 12 carbon atoms, such as methoxycarbonyl, Ethoxycarbonyl, etc.), aryloxycarbonyl group (preferably Alternatively, it has 7 to 30 carbon atoms, more preferably 7 to 20 carbon atoms, and particularly preferably 7 to 12 carbon atoms, and examples thereof include phenyloxycarbonyl. ), An acyloxy group (preferably having 2 to 30 carbon atoms, more preferably 2 to 20 carbon atoms, particularly preferably 2 to 10 carbon atoms such as acetoxy and benzoyloxy), an acylamino group (preferably 2-30 carbon atoms, more preferably 2-20 carbon atoms, particularly preferably 2-10 carbon atoms, and examples thereof include acetylamino, benzoylamino, and the like, and an alkoxycarbonylamino group (preferably having 2-2 carbon atoms). 30, more preferably 2 to 20 carbon atoms, particularly preferably 2 to 12 carbon atoms, such as methoxycarbonylamino, etc.), aryloxycarbonylamino group (preferably 7 to 30 carbon atoms, more preferably 7 to 20 carbon atoms, particularly preferably 7 to 12 carbon atoms, such as phenyloxycarbonyl And sulfonylamino groups (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, and particularly preferably 1 to 12 carbon atoms, such as methanesulfonylamino and benzenesulfonylamino). ), A sulfamoyl group (preferably having 0 to 30 carbon atoms, more preferably 0 to 20 carbon atoms, particularly preferably 0 to 12 carbon atoms, such as sulfamoyl, methylsulfamoyl, dimethylsulfamoyl, phenyl Sulfamoyl, etc.), a carbamoyl group (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 12 carbon atoms, such as carbamoyl, methylcarbamoyl, diethylcarbamoyl, Phenylcarbamoyl etc.), alkylthio group ( Preferably, it has 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 12 carbon atoms, and examples thereof include methylthio, ethylthio and the like, and an arylthio group (preferably 6 to 30 carbon atoms). , More preferably 6 to 20 carbon atoms, particularly preferably 6 to 12 carbon atoms, such as phenylthio, etc.), a heterocyclic thio group (preferably 1 to 30 carbon atoms, more preferably 1 to carbon atoms). 20, particularly preferably 1 to 12 carbon atoms, such as pyridylthio, 2-benzimidazolylthio, 2-benzoxazolylthio, 2-benzthiazolylthio and the like, and a sulfonyl group (preferably having a carbon number). 1 to 30, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 12 carbon atoms, such as mesyl and tosyl). Rufinyl group (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 12 carbon atoms, and examples thereof include methanesulfinyl and benzenesulfinyl. ), A ureido group (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, and particularly preferably 1 to 12 carbon atoms, such as ureido, methylureido, phenylureido, etc.), phosphoric acid. An amide group (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 12 carbon atoms, such as diethyl phosphoric acid amide and phenylphosphoric acid amide), a hydroxy group , Mercapto group, halogen atom (eg fluorine atom, chlorine atom, bromine atom, iodine atom), cyano group, sulfo group, carboxyl group, nitro group, hydroxamic acid group, sulfino group, hydrazino group, imino group, heterocyclic group ( Preferably it is C1-C30, More preferably, it is C1-C12, As a hetero atom, for example, a nitrogen atom, oxygen And specifically a imidazolyl, pyridyl, quinolyl, furyl, thienyl, piperidyl, morpholino, benzoxazolyl, benzimidazolyl, benzthiazolyl, carbazolyl group, azepinyl group, and the like. Preferably, it has 3 to 40 carbon atoms, more preferably 3 to 30 carbon atoms, and particularly preferably 3 to 24 carbon atoms, and examples thereof include trimethylsilyl, triphenylsilyl and the like, and a silyloxy group (preferably 3 to 3 carbon atoms). 40, more preferably 3 to 30 carbon atoms, particularly preferably 3 to 24 carbon atoms, and examples thereof include trimethylsilyloxy and triphenylsilyloxy.

The aromatic hydrocarbon ring or aromatic heterocycle represented by Ar ^{1 to} Ar ⁵ may further form a condensed ring with another ring. Examples of the condensed ring include a benzene ring, a pyridine ring, a pyrazine ring, and a pyrimidine. Ring, pyridazine ring, pyrrole ring, pyrazole ring, imidazole ring, triazole ring, oxazole ring, oxadiazole ring, thiazole ring, thiadiazole ring, furan ring, thiophene ring, selenophene ring, silole ring, germol ring, phosphole ring, etc. Can be mentioned.
The above substituent and condensed ring may further have a substituent and may be further condensed with another ring.

The aromatic hydrocarbon ring or aromatic heterocycle represented by Ar ^{1 to} Ar ⁵ is preferably a benzene ring, pyridine ring, pyrazine ring, pyrimidine ring, triazine ring, pyrrole ring, pyrazole ring, imidazole ring, triazole ring, Oxazole ring, thiazole ring, furan ring, thiophene ring, more preferably benzene ring, pyridine ring, pyrazine ring, pyrrole ring, pyrazole ring, imidazole ring, oxazole ring, thiazole ring, thiophene ring, more preferably , A benzene ring, a pyridine ring, a pyrazine ring, a pyrazole ring, an imidazole ring and a thiophene ring, particularly preferably a benzene ring, a pyridine ring and a pyrazine ring.

Ar ^{1 to} Ar ⁵ may be linked at the same or different positions. Even if they are linked by adjacent atoms (ortho position in the case of a benzene ring), they may be linked by an atom sandwiching one atom (if it is a benzene ring). (Meta-position), two atoms connected by an intervening atom (in the case of a benzene ring, para-position), or further, an atom may be connected by an intervening atom.

The aromatic hydrocarbon ring or aromatic heterocycle formed from Q is not particularly limited, but is preferably a 4- to 10-membered ring, more preferably a 5- to 7-membered ring, still more preferably 5- and 6-membered rings, and 6-membered A ring is particularly preferred. The heteroatom contained in the aromatic heterocycle formed from Q is not particularly limited, but an aromatic heterocycle containing nitrogen, oxygen, sulfur, selenium, silicon, germanium or phosphorus is preferred, and nitrogen, oxygen or sulfur is more preferred. More preferred are nitrogen and oxygen, and particularly preferred is nitrogen. The number of heteroatoms contained in one aromatic heterocycle formed from Q is not particularly limited, but is preferably 1 to 3.
Specific examples of the aromatic hydrocarbon ring or aromatic heterocycle formed from Q include benzene ring, pyridine ring, pyrazine ring, pyrimidine ring, pyridazine ring, pyrrole ring, pyrazole ring, imidazole ring, triazole ring, oxazole ring. Oxadiazole ring, thiazole ring, thiadiazole ring, furan ring, thiophene ring, selenophene ring, silole ring, germol ring, phosphole ring and the like.
The aromatic hydrocarbon ring or aromatic heterocycle formed from Q may have a substituent, and the substituents listed above as the substituent group A can be applied.

The aromatic hydrocarbon ring or aromatic heterocycle formed from Q may further form a condensed ring with another ring. Examples of the condensed ring include a benzene ring, a pyridine ring, a pyrazine ring, a pyrimidine ring, and a pyridazine ring. , Pyrrole ring, pyrazole ring, imidazole ring, triazole ring, oxazole ring, oxadiazole ring, thiazole ring, thiadiazole ring, furan ring, thiophene ring, selenophene ring, silole ring, gelmol ring, phosphole ring and the like.
The above substituent and condensed ring may further have a substituent and may be further condensed with another ring.

The aromatic hydrocarbon ring or aromatic heterocycle formed from Q is preferably a benzene ring, pyridine ring, pyrazine ring, pyrimidine ring, triazine ring, pyrrole ring, pyrazole ring, imidazole ring, triazole ring, oxazole ring, thiazole. Ring, furan ring, thiophene ring, more preferably benzene ring, pyridine ring, pyrazine ring, pyrrole ring, pyrazole ring, imidazole ring, oxazole ring, thiazole ring, thiophene ring, more preferably benzene ring, A pyridine ring, a pyrazine ring, a pyrazole ring, an imidazole ring, and a thiophene ring are preferable, and a benzene ring, a pyridine ring, and a pyrazine ring are particularly preferable.
Among the aromatic hydrocarbon rings or aromatic heterocycles represented by Ar ^{1 to} Ar ⁵ , at least one of the aromatic hydrocarbon rings or aromatic heterocycles formed from Q may be an aromatic heterocycle preferable.

  The compound represented by the general formula (I) is more preferably a compound represented by the following general formula (II).

(In the general formula (II), Ar ²¹ and Ar ²² represent an aromatic hydrocarbon ring or an aromatic heterocycle. A ^{1 to} A ¹⁶ represent C—R ²¹ or N. R ²¹ represents a hydrogen atom or a substituent. A plurality of R ²¹ may be the same or different.)

The general formula (II) will be described. Ar ²¹ and Ar ²² are synonymous with the aromatic hydrocarbon ring or aromatic heterocycle represented by Ar ^{1 to} Ar ⁵ in the general formula (I), and the preferred range is also the same. A ^{1 to} A ¹⁶ represent C—R ²¹ or N. R ²¹ represents a hydrogen atom or a substituent. As the substituent represented by R ²¹ , those exemplified as the substituent group A can be applied, and preferred ranges thereof are also the same.

  One of the preferable forms of the compound represented by general formula (I) and general formula (II) is a compound represented by the following general formula (III).

(In general formula (III), Ar ³¹ and Ar ³² represent an aromatic hydrocarbon ring or an aromatic heterocycle. R ^{1 to} R ¹⁶ represent a hydrogen atom or a substituent.)

The general formula (III) will be described. Ar ³¹ and Ar ³² are synonymous with Ar ²¹ and Ar ²² in formula (II), and preferred ranges are also the same. R ^{1 to} R ¹⁶ represent a hydrogen atom or a substituent. As the substituents represented by R ^{1 to} R ¹⁶ , those exemplified as the substituent group A can be applied. R ^{1 to} R ¹⁶ are preferably a hydrogen atom, alkyl group, aryl group, amino group, alkoxy group, aryloxy group, heterocyclic oxy group, alkylthio group, arylthio group, heterocyclic thio group, fluorine group, chlorine group, Bromine group, iodine group, cyano group, heterocyclic group, silyl group, silyloxy group, more preferably a hydrogen atom, alkyl group, aryl group, amino group, fluorine group, cyano group, heterocyclic group, silyl group More preferably a hydrogen atom, an alkyl group, an aryl group, a fluorine group, a cyano group, a heterocyclic group or a silyl group, and particularly preferably a hydrogen atom, an alkyl group, an aryl group or a heterocyclic group.

  The compound represented by the general formula (III) is more preferably a compound represented by the following general formula (IV) or general formula (V).

(In general formula (IV), R ^{1 to} R ²⁰ represent a hydrogen atom or a substituent. X ^{1 to} X ⁴ represent an N atom or C—R ⁴¹ , and R ⁴¹ represents a hydrogen atom or a substituent.)

(In general formula (V), R ^{1 to} R ¹⁶ and R ^{21 to} R ²⁴ represent a hydrogen atom or a substituent. X ^{5 to} X ⁸ represent an N atom or C—R ⁵¹ , and R ⁵¹ represents a hydrogen atom or Represents a substituent.)

The general formula (IV) will be described. R ^{1 to} R ¹⁶ have the same meanings as those in formula (III), and preferred ranges are also the same. R ^{17 to} R ²⁰ represent a hydrogen atom or a substituent, and examples and preferred ranges thereof are the same as those of R ^{1 to} R ¹⁶ . X ^{1 to} X ^{4 each} represents an N atom or C—R ⁴¹ . Among X ^{1 to} X ⁴ , 1 to 2 are preferably N atoms. R ⁴¹ represents a hydrogen atom or a substituent, and examples and preferred ranges thereof are the same as those for R ^{1 to} R ¹⁶ .

The general formula (V) will be described. R ^{1 to} R ¹⁶ have the same meanings as those in formula (III), and preferred ranges are also the same. R ^{21 to} R ²⁴ represent a hydrogen atom or a substituent, and examples and preferred ranges thereof are the same as those of R ^{1 to} R ¹⁶ . X ^{5 to} X ^{8 each} represents an N atom or C—R ⁵¹ . Among X ^{5 to} X ⁸ , 1 to 2 are preferably N atoms. R ⁵¹ represents a hydrogen atom or a substituent, and examples and preferred ranges thereof are the same as those for R ^{1 to} R ¹⁶ .

Specific examples of the compounds represented by the general formulas (I) to (V) are shown below, but the present invention is not limited to these. (Ph represents a phenyl group, and ^t Bu represents a tertiary butyl group).

  The compounds represented by the general formulas (I) to (V) of the present invention can be synthesized by various known synthesis methods. For example, Exemplified Compound 1 can be synthesized by the method described in Justus Liebigs Annalen der Chemie, 751, 1-16 (1971). Alternatively, it can also be synthesized by the method described in Journal of American Chemistry Society, 127, 13732-13737 (2005). For example, exemplary compound 127 can be synthesized according to the following scheme.

  Considering the durability of the device, the glass transition temperature (Tg) of the compound of the present invention is preferably 130 ° C. or higher and 450 ° C. or lower, more preferably 135 ° C. or higher and 450 ° C. or lower, and still more preferably. It is 140 degreeC or more and 450 degrees C or less, Especially preferably, they are 150 degreeC or more and 450 degrees C or less, Most preferably, they are 160 degreeC or more and 450 degrees C or less.

  Here, Tg can be confirmed by thermal measurement such as differential scanning calorimetry (DSC) and differential thermal analysis (DTA), X-ray diffraction (XRD), and polarization microscope observation.

When the element of the present invention is a light emitting element utilizing phosphorescence, the lowest excited triplet energy level (T ₁ level) of the compound of the present invention is 65 kcal / mol (272.35 kJ / mol) or more and 95 kcal. / Mol (398.05 kJ / mol) or less, preferably 67 kcal / mol (280.73 kJ / mol) or more and 95 kcal / mol (398.05 kJ / mol) or less, more preferably 69 kcal / mol (289.11 kJ / mol). As described above, 95 kcal / mol (398.05 kJ / mol) or less is more preferable.

Here, the T ₁ level can be obtained from the short wavelength end of the phosphorescence emission spectrum of the thin film of the material.

  Next, elements constituting the element of the present invention will be described in detail.

<Board>
The substrate used in the present invention is preferably a substrate that does not scatter or attenuate light emitted from the organic compound layer. Specific examples thereof include zirconia stabilized yttrium (YSZ), inorganic materials such as glass, polyesters such as polyethylene terephthalate, polybutylene phthalate, and polyethylene naphthalate, polystyrene, polycarbonate, polyethersulfone, polyarylate, polyimide, and polycycloolefin. , Organic materials such as norbornene resin and poly (chlorotrifluoroethylene).
For example, when glass is used as the substrate, it is preferable to use non-alkali glass as the material in order to reduce ions eluted from the glass. Moreover, when using soda-lime glass, it is preferable to use what gave barrier coatings, such as a silica. In the case of an organic material, it is preferable that it is excellent in heat resistance, dimensional stability, solvent resistance, electrical insulation, and workability.

  There is no restriction | limiting in particular about the shape of a board | substrate, a structure, a magnitude | size, It can select suitably according to the use, purpose, etc. of a light emitting element. In general, the shape of the substrate is preferably a plate shape. The structure of the substrate may be a single layer structure, a laminated structure, may be formed of a single member, or may be formed of two or more members.

  The substrate may be colorless and transparent or colored and transparent, but is preferably colorless and transparent in that it does not scatter or attenuate light emitted from the organic light emitting layer.

The substrate can be provided with a moisture permeation preventing layer (gas barrier layer) on the front surface or the back surface.
As a material for the moisture permeation preventive layer (gas barrier layer), inorganic materials such as silicon nitride and silicon oxide are preferably used. The moisture permeation preventing layer (gas barrier layer) can be formed by, for example, a high frequency sputtering method.
When a thermoplastic substrate is used, a hard coat layer, an undercoat layer, or the like may be further provided as necessary.

<Anode>
The anode usually has a function as an electrode for supplying holes to the organic compound layer, and there is no particular limitation on the shape, structure, size, etc., depending on the use and purpose of the light-emitting element. , Can be appropriately selected from known electrode materials. As described above, the anode is usually provided as a transparent anode.

  Suitable examples of the material for the anode include metals, alloys, metal oxides, conductive compounds, and mixtures thereof. Specific examples of the anode material include conductive metals such as tin oxide (ATO, FTO) doped with antimony or fluorine, tin oxide, zinc oxide, indium oxide, indium tin oxide (ITO), indium zinc oxide (IZO), etc. Metals such as oxides, gold, silver, chromium, nickel, and mixtures or laminates of these metals and conductive metal oxides, inorganic conductive materials such as copper iodide and copper sulfide, polyaniline, polythiophene, polypyrrole, etc. Organic conductive materials, and a laminate of these and ITO. Among these, conductive metal oxides are preferable, and ITO is particularly preferable from the viewpoints of productivity, high conductivity, transparency, and the like.

  The anode is composed of, for example, a wet method such as a printing method and a coating method, a physical method such as a vacuum deposition method, a sputtering method, and an ion plating method, and a chemical method such as a CVD and a plasma CVD method. It can be formed on the substrate according to a method appropriately selected in consideration of suitability with the material to be processed. For example, when ITO is selected as the anode material, the anode can be formed according to a direct current or high frequency sputtering method, a vacuum deposition method, an ion plating method, or the like.

  In the organic electroluminescent element of the present invention, the formation position of the anode is not particularly limited and can be appropriately selected according to the use and purpose of the light emitting element, but it is preferably formed on the substrate. In this case, the anode may be formed on the entire one surface of the substrate, or may be formed on a part thereof.

  The patterning for forming the anode may be performed by chemical etching such as photolithography, or may be performed by physical etching such as laser, or vacuum deposition or sputtering with a mask overlapped. It may be performed by a lift-off method or a printing method.

  The thickness of the anode can be appropriately selected depending on the material constituting the anode and cannot be generally defined, but is usually about 10 nm to 50 μm, and preferably 50 nm to 20 μm.

The resistance value of the anode is preferably 10 ³ Ω / □ or less, and more preferably 10 ² Ω / □ or less. When the anode is transparent, it may be colorless and transparent or colored and transparent. In order to take out light emission from the transparent anode side, the transmittance is preferably 60% or more, and more preferably 70% or more.

  The transparent anode is described in detail in the book “New Development of Transparent Electrode Films” published by CMC (1999), supervised by Yutaka Sawada, and the matters described here can be applied to the present invention. In the case of using a plastic substrate having low heat resistance, a transparent anode formed using ITO or IZO at a low temperature of 150 ° C. or lower is preferable.

<Cathode>
The cathode usually has a function as an electrode for injecting electrons into the organic compound layer, and there is no particular limitation on the shape, structure, size, etc., depending on the use and purpose of the light-emitting element, It can select suitably from well-known electrode materials.

  Examples of the material constituting the cathode include metals, alloys, metal oxides, electrically conductive compounds, and mixtures thereof. Specific examples include alkali metals (eg, Li, Na, K, Cs, etc.), alkaline earth metals (eg, Mg, Ca, etc.), gold, silver, lead, aluminum, sodium-potassium alloys, lithium-aluminum alloys, magnesium. -Rare earth metals such as silver alloys, indium, ytterbium, and the like. These may be used alone, but two or more can be suitably used in combination from the viewpoint of achieving both stability and electron injection.

Among these, as a material constituting the cathode, an alkali metal or an alkaline earth metal is preferable from the viewpoint of electron injecting property, and a material mainly composed of aluminum is preferable from the viewpoint of excellent storage stability.
The material mainly composed of aluminum is aluminum alone, an alloy of aluminum and 0.01 to 10% by mass of alkali metal or alkaline earth metal, or a mixture thereof (for example, lithium-aluminum alloy, magnesium-aluminum alloy, etc.) Say.

  The materials for the cathode are described in detail in JP-A-2-15595 and JP-A-5-121172, and the materials described in these public relations can also be applied in the present invention.

  There is no restriction | limiting in particular about the formation method of a cathode, According to a well-known method, it can carry out. For example, the cathode described above is configured from a wet method such as a printing method or a coating method, a physical method such as a vacuum deposition method, a sputtering method, or an ion plating method, or a chemical method such as CVD or plasma CVD method. It can be formed according to a method appropriately selected in consideration of suitability with the material. For example, when a metal or the like is selected as the cathode material, one or more of them can be simultaneously or sequentially performed according to a sputtering method or the like.

  Patterning when forming the cathode may be performed by chemical etching such as photolithography, physical etching by laser, or the like, or by vacuum deposition or sputtering with the mask overlaid. It may be performed by a lift-off method or a printing method.

In the present invention, the cathode formation position is not particularly limited, and may be formed on the entire organic compound layer or a part thereof.
Further, a dielectric layer made of an alkali metal or alkaline earth metal fluoride or oxide may be inserted between the cathode and the organic compound layer with a thickness of 0.1 to 5 nm. This dielectric layer can also be regarded as a kind of electron injection layer. The dielectric layer can be formed by, for example, a vacuum deposition method, a sputtering method, an ion plating method, or the like.

The thickness of the cathode can be appropriately selected depending on the material constituting the cathode and cannot be generally defined, but is usually about 10 nm to 5 μm, and preferably 50 nm to 1 μm.
Further, the cathode may be transparent or opaque. The transparent cathode can be formed by depositing a thin cathode material to a thickness of 1 to 10 nm and further laminating a transparent conductive material such as ITO or IZO.

<Organic compound layer>
The organic compound layer in the present invention will be described.
The organic electroluminescent element of the present invention has at least one organic compound layer including a light emitting layer between a pair of electrodes. As the organic compound layer other than the organic light emitting layer, as described above, a hole is formed. Examples include a transport layer, an electron transport layer, a charge blocking layer, a hole injection layer, and an electron injection layer.

-Formation of organic compound layer-
In the organic electroluminescent element of the present invention, each layer constituting the organic compound layer can be suitably formed by any of a dry film forming method such as a vapor deposition method and a sputtering method, a transfer method, and a printing method.

-Organic light emitting layer-
The organic light emitting layer receives holes from the anode, the hole injection layer, or the hole transport layer when an electric field is applied, receives electrons from the cathode, the electron injection layer, or the electron transport layer, and recombines holes and electrons. It is a layer having a function of providing a field to emit light.
The light emitting layer in the present invention may be composed of only a light emitting material, or may be a mixed layer of a host material and a light emitting material. The light emitting material may be a fluorescent light emitting material or a phosphorescent light emitting material, and the dopant may be one type or two or more types. The host material is preferably a charge transport material. The host material may be one type or two or more types, and examples thereof include a configuration in which an electron transporting host material and a hole transporting host material are mixed. Further, the light emitting layer may include a material that does not have charge transporting properties and does not emit light.
Further, the light emitting layer may be a single layer or two or more layers, and each layer may emit light in different emission colors.

  Examples of fluorescent materials that can be used in the present invention include, for example, benzoxazole derivatives, benzimidazole derivatives, benzothiazole 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, cyclopentadiene derivatives, styryl Of amine derivatives, diketopyrrolopyrrole derivatives, aromatic dimethylidin compounds, metal complexes of 8-quinolinol derivatives and pyromethene derivatives And various metal complexes typified by metal complex, polythiophene, polyphenylene, polyphenylene vinylene polymer compounds include compounds such as organic silane derivatives.

Examples of the phosphorescent material that can be used in the present invention include complexes containing transition metal atoms or lanthanoid atoms.
Although it does not specifically limit as a transition metal atom, Preferably, ruthenium, rhodium, palladium, tungsten, rhenium, osmium, iridium, and platinum are mentioned, More preferably, they are rhenium, iridium, and platinum.
Examples of lanthanoid atoms include lanthanum, cerium, praseodymium, neodymium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, and lutetium. Among these lanthanoid atoms, neodymium, europium, and gadolinium are preferable.

Examples of complex ligands include G. Wilkinson et al., Comprehensive Coordination Chemistry, published by Pergamon Press, 1987, H. Yersin, “Photochemistry and Photophysics of Coordination Compounds,” Springer-Verlag, 1987, Akio Yamamoto. Examples of the ligands described in the book “Organic Metal Chemistry-Fundamentals and Applications-” published in 1982 by Hankabosha.
Specific ligands are preferably halogen ligands (preferably chlorine ligands), nitrogen-containing heterocyclic ligands (eg, phenylpyridine, benzoquinoline, quinolinol, bipyridyl, phenanthroline, etc.), diketones Ligand (for example, acetylacetone), carboxylic acid ligand (for example, acetic acid ligand), carbon monoxide ligand, isonitrile ligand, cyano ligand, more preferably nitrogen-containing Heterocyclic ligand. The complex may have one transition metal atom in the compound, or may be a so-called binuclear complex having two or more. Different metal atoms may be contained at the same time.

  The phosphorescent material is preferably an iridium complex or a platinum complex, particularly a tetradentate platinum complex or an iridium complex having a fluorine-substituted phenylpyridine as a ligand.

  The phosphorescent material is preferably contained in the light emitting layer in an amount of 0.1 to 40% by mass, and more preferably 0.5 to 20% by mass.

  The host material contained in the light emitting layer in the present invention includes, in addition to the compound of the present invention, for example, those having a carbazole skeleton, those having a diarylamine skeleton, those having a pyridine skeleton, those having a pyrazine skeleton, Examples thereof include those having a triazine skeleton and those having an arylsilane skeleton, and materials exemplified in the sections of a hole injection layer, a hole transport layer, an electron injection layer, and an electron transport layer described later.

  Although the thickness of a light emitting layer is not specifically limited, Usually, it is preferable that they are 1 nm-500 nm, it is more preferable that they are 5 nm-200 nm, and it is still more preferable that they are 10 nm-100 nm.

-Hole injection layer, hole transport layer-
The hole injection layer and the hole transport layer are layers having a function of receiving holes from the anode or the anode side and transporting them to the cathode side. Specifically, the hole injection layer and the hole transport layer are carbazole derivatives, triazole derivatives, oxazole derivatives, oxadiazole derivatives, imidazole derivatives, polyarylalkane derivatives, pyrazoline derivatives, pyrazolone derivatives, phenylenediamine derivatives, arylamines. Derivatives, amino-substituted chalcone derivatives, styrylanthracene derivatives, fluorenone derivatives, hydrazone derivatives, stilbene derivatives, silazane derivatives, aromatic tertiary amine compounds, styrylamine compounds, aromatic dimethylidin compounds, porphyrin compounds, organosilane derivatives, carbon , Etc. are preferable.
The thicknesses of the hole injection layer and the hole transport layer are each preferably 500 nm or less from the viewpoint of lowering the driving voltage.
The thickness of the hole transport layer is preferably 1 nm to 500 nm, more preferably 5 nm to 200 nm, and still more preferably 10 nm to 100 nm. In addition, the thickness of the hole injection layer is preferably 0.1 nm to 200 nm, more preferably 0.5 nm to 100 nm, and still more preferably 1 nm to 100 nm.
The hole injection layer and the hole transport layer may have a single-layer structure composed of one or more of the materials described above, or may have a multilayer structure composed of a plurality of layers having the same composition or different compositions. .

-Electron injection layer, electron transport layer-
The electron injection layer and the electron transport layer are layers having a function of receiving electrons from the cathode or the cathode side and transporting them to the anode side. Specifically, the electron injection layer and the electron transport layer are a triazole derivative, an oxazole derivative, an oxadiazole derivative, an imidazole derivative, a fluorenone derivative, an anthraquinodimethane derivative, an anthrone derivative, a diphenylquinone derivative in addition to the compound of the present invention. Thiopyran dioxide derivatives, carbodiimide derivatives, fluorenylidenemethane derivatives, distyrylpyrazine derivatives, aromatic tetracarboxylic anhydrides such as naphthalene and perylene, phthalocyanine derivatives, metal complexes of 8-quinolinol derivatives, metal phthalocyanines, benzoxazoles And a layer containing various metal complexes represented by metal complexes having benzothiazole as a ligand, organosilane derivatives, and the like.

The thicknesses of the electron injection layer and the electron transport layer are each preferably 500 nm or less from the viewpoint of lowering the driving voltage.
The thickness of the electron transport layer is preferably 1 nm to 500 nm, more preferably 5 nm to 200 nm, and still more preferably 10 nm to 100 nm. In addition, the thickness of the electron injection layer is preferably 0.1 nm to 200 nm, more preferably 0.2 nm to 100 nm, and still more preferably 0.5 nm to 50 nm.
The electron injection layer and the electron transport layer may have a single layer structure composed of one or more of the above-described materials, or may have a multilayer structure composed of a plurality of layers having the same composition or different compositions.

-Hole blocking layer-
The hole blocking layer is a layer having a function of preventing holes transported from the anode side to the light emitting layer from passing through to the cathode side. In the present invention, a hole blocking layer can be provided as an organic compound layer adjacent to the light emitting layer on the cathode side.
Examples of the organic compound constituting the hole blocking layer include the compound of the present invention, an aluminum complex such as BAlq, a triazole derivative, and a phenanthroline derivative such as BCP.
The thickness of the hole blocking layer is preferably 1 nm to 500 nm, more preferably 5 nm to 200 nm, and still more preferably 10 nm to 100 nm.
The hole blocking layer may have a single layer structure composed of one or more of the above-described materials, or may have a multilayer structure composed of a plurality of layers having the same composition or different compositions.

<Protective layer>
In the present invention, the entire organic EL element may be protected by a protective layer.
As a material contained in the protective layer, any material may be used as long as it has a function of preventing materials that promote device deterioration such as moisture and oxygen from entering the device.
Specific examples thereof include metals such as In, Sn, Pb, Au, Cu, Ag, Al, Ti, and Ni, MgO, SiO, SiO ₂ , Al ₂ O ₃ , GeO, NiO, CaO, BaO, and Fe ₂ O. ₃ , metal oxides such as Y ₂ O ₃ and TiO ₂ , metal nitrides such as SiN _x and SiN _x O _y , metal fluorides such as MgF ₂ , LiF, AlF ₃ and CaF ₂ , polyethylene, polypropylene, polymethyl Monomer mixture containing methacrylate, polyimide, polyurea, polytetrafluoroethylene, polychlorotrifluoroethylene, polydichlorodifluoroethylene, copolymer of chlorotrifluoroethylene and dichlorodifluoroethylene, tetrafluoroethylene and at least one comonomer A copolymer obtained by copolymerization of a copolymer having a cyclic structure in the copolymer main chain. Copolymer, 1% by weight of the water absorbing water absorption material, water absorption of 0.1% or less of moisture-proof material, and the like.

  The method for forming the protective layer is not particularly limited, and for example, vacuum deposition, sputtering, reactive sputtering, MBE (molecular beam epitaxy), cluster ion beam, ion plating, plasma polymerization (high frequency) Excited ion plating method), plasma CVD method, laser CVD method, thermal CVD method, gas source CVD method, coating method, printing method, transfer method can be applied.

<Sealing>
Furthermore, the organic electroluminescent element of this invention may seal the whole element using a sealing container.
Further, a moisture absorbent or an inert liquid may be sealed in a space between the sealing container and the light emitting element. Although it does not specifically limit as a moisture absorber, For example, barium oxide, sodium oxide, potassium oxide, calcium oxide, sodium sulfate, calcium sulfate, magnesium sulfate, phosphorus pentoxide, calcium chloride, magnesium chloride, copper chloride Cesium fluoride, niobium fluoride, calcium bromide, vanadium bromide, molecular sieve, zeolite, magnesium oxide and the like. The inert liquid is not particularly limited, and examples thereof include fluorinated solvents such as paraffins, liquid paraffins, perfluoroalkanes, perfluoroamines, perfluoroethers, chlorinated solvents, and silicone oils. It is done.

The organic electroluminescence device of the present invention emits light by applying a direct current (which may include an alternating current component as necessary) voltage (usually 2 to 15 volts) or a direct current between the anode and the cathode. Obtainable.
The driving method of the organic electroluminescence device of the present invention is described in JP-A-2-148687, JP-A-6-301355, JP-A-5-29080, JP-A-7-134558, JP-A-8-234658, and JP-A-8-2441047. The driving method described in each publication, Japanese Patent No. 2784615, US Pat. Nos. 5,828,429, 6023308, and the like can be applied.

<Comparative Example 1>
A glass substrate having an ITO film of 0.5 mm thickness and 2.5 cm square (manufactured by Geomatek Co., Ltd., surface resistance 10 Ω / □) is placed in a cleaning container, ultrasonically cleaned in 2-propanol, and then subjected to UV-ozone treatment for 30 minutes. Went. The following organic compound layers were sequentially deposited on the transparent anode (ITO film) by vacuum deposition.
The vapor deposition rate in the examples of the present invention is 0.2 nm / second unless otherwise specified. The deposition rate was measured using a quartz resonator. The film thicknesses described below were also measured using a crystal resonator.

(First hole transport layer)
Copper phthalocyanine: film thickness 10nm
(Second hole transport layer)
NPD: film thickness 40nm
(Light emitting layer)
CBP = 90% by mass, Ferric layer: film thickness 30 nm
(First electron transport layer)
BAlq: film thickness 10 nm
(Second electron transport layer)
Alq: film thickness 10 nm

Finally, lithium fluoride 0.1 nm and metal aluminum 100 nm were deposited in this order to form a cathode.
This is put in a glove box substituted with argon gas without being exposed to the atmosphere, and sealed with a stainless steel sealing can and an ultraviolet curable adhesive (XNR5516HV, manufactured by Nagase Ciba Co., Ltd.). Thus, an organic electroluminescent element of Comparative Example 1 was obtained.

<Comparative example 2>
Except for changing CBP to compound (XVI) [compound described in Patent Document 3 (Japanese Patent Laid-Open No. 2002-356449)], the organic electroluminescent element of <Comparative Example 1> was subjected to the same method as that of Comparative Example 2. An organic electroluminescent element was produced.

  The chemical structures of copper phthalocyanine, NPD, CBP, Firpic, Alq, BAlq, and compound (XVI) used in the comparative example are shown below.

<Example 1>
The organic electroluminescent element of Example 1 was produced in the same manner as the organic electroluminescent element of <Comparative Example 1> except that CBP was changed to the exemplified compound 2 of the present invention.

<Example 2>
An organic electroluminescent device of Example 2 was produced in the same manner as the organic electroluminescent device of <Comparative Example 1> except that CBP was changed to Exemplified Compound 8 of the present invention.

<Example 3>
An organic electroluminescent device of Example 3 was produced in the same manner as the organic electroluminescent device of <Comparative Example 1> except that CBP was changed to the exemplified compound 29 of the present invention.

<Example 4>
An organic electroluminescent device of Example 4 was produced in the same manner as the organic electroluminescent device of <Comparative Example 1> except that CBP was changed to the exemplified compound 31 of the present invention.

When a voltage of 10 V was applied to the elements of Examples 1 to 4, Comparative Example 1 and Comparative Example 2, the light emitting elements of Examples 1 to 4 and Comparative Example 1 obtained light emission derived from Ferpic. In the device of Example 2, no luminescence derived from Ferpic was observed.
Table 1 shows the relative ratio of the luminance when the elements of Examples 1 to 4 and Comparative Example 1 are driven with an applied voltage of 10 V, and the luminance half time of the elements of Examples 1 to 4 and Comparative Example 1. Luminance half-time is set in the OLED test system ST-D type manufactured by Tokyo System Development Co., Ltd., and is driven in constant current mode under the condition of positive current constant 0.4 mA. The luminance is 50% of the initial luminance. It was measured as the time t _0.5 until drops.

<Example 5>
An organic electroluminescent element of Example 5 was produced in the same manner as the organic electroluminescent element of <Comparative Example 1> except that BAlq was changed to Exemplified Compound 8 of the present invention.
When the elements of Example 5 and Comparative Example 1 were driven with an applied voltage of 10 V, the relative luminance ratio was 5: 1.

  As is clear from the above examples, an organic electroluminescent device having high efficiency and high durability can be obtained by using the compound of the present invention.

Claims (10)

An organic electroluminescence device having at least one organic compound layer including a light emitting layer containing a light emitting material between a pair of electrodes, wherein at least one compound represented by the following general formula (I) is used as the organic compound layer An organic electroluminescent element characterized by containing.

(In the general formula (I), Ar ^{1 to} Ar ⁵ represent an aromatic hydrocarbon ring or an aromatic heterocycle. Q represents an atomic group necessary for forming an aromatic hydrocarbon ring or an aromatic heterocycle. .) The organic electroluminescent element according to claim 1, wherein the compound represented by the general formula (I) is represented by the following general formula (II).

(In the general formula (II), Ar ²¹ and Ar ²² represent an aromatic hydrocarbon ring or an aromatic heterocycle. A ^{1 to} A ¹⁶ represent C—R ²¹ or N. R ²¹ represents a hydrogen atom or a substituent. A plurality of R ²¹ may be the same or different.) The organic electroluminescent element according to claim 2, wherein the compound represented by the general formula (II) is represented by the following general formula (III).

(In general formula (III), Ar ³¹ and Ar ³² represent an aromatic hydrocarbon ring or an aromatic heterocycle. R ^{1 to} R ¹⁶ represent a hydrogen atom or a substituent.) The organic electroluminescent element according to claim 3, wherein the compound represented by the general formula (III) is represented by the following general formula (IV).

(In general formula (IV), R ^{1 to} R ²⁰ represent a hydrogen atom or a substituent. X ^{1 to} X ⁴ represent an N atom or C—R ⁴¹ , and R ⁴¹ represents a hydrogen atom or a substituent.) The organic electroluminescent element according to claim 3, wherein the compound represented by the general formula (III) is represented by the following general formula (V).

(In the general formula (V), R ^{1 to} R ¹⁶ and R ^{21 to} R ²⁴ represent a hydrogen atom or a substituent. X ^{5 to} X ⁸ represent an N atom or C—R ⁵¹ , and R ⁵¹ represents a hydrogen atom or Represents a substituent.)   The organic electroluminescence device according to any one of claims 1 to 5, wherein the compounds represented by the general formulas (I) to (V) have a glass transition temperature of 130 ° C or higher and 450 ° C or lower.   The lowest excited triplet energy level of the compounds represented by the general formulas (I) to (V) is 65 kcal / mol (272.35 kJ / mol) or more and 95 kcal / mol (398.05 kJ / mol) or less. The organic electroluminescent element according to any one of claims 1 to 6.   8. The organic electroluminescent element according to claim 1, wherein at least one of the light emitting materials is a phosphorescent light emitting material.   The organic electroluminescent element according to claim 8, wherein the phosphorescent material is an iridium complex or a platinum complex.   The organic electroluminescent element according to any one of claims 1 to 9, wherein the light emitting layer contains a compound represented by the general formulas (I) to (V).