JP2008239797A - Organic electroluminescent device - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an organic electroluminescent device having a high luminous efficiency and a high durability, to be driven by a low voltage. <P>SOLUTION: The organic electroluminescent device comprises at least one organic compound layer including an emitter layer containing a luminescent material between a pair of electrodes. The organic compound layer contains a sulfoxide compound of a cyclic structure. The sulfoxide compound is a sulfonyl compound synthesized according to reaction of the figure. The silicon portion as a linking group may be absent, a single bond or another linking group. The sulfonyl group portion may be an S atom or a sulfinyl group. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

  The present invention relates to an organic electroluminescent element (hereinafter also referred to as “organic EL element”) that can emit light by converting electric energy into light.

  In recent years, organic electroluminescence devices have been actively researched and developed because they can emit light with high luminance when driven at a low voltage. In general, an organic EL device has an organic compound layer between a pair of electrodes. Electrons injected from the cathode and holes injected from the anode recombine in the light emitting layer, and the generated exciton energy is used for light emission. To do.

  In recent years, the use of phosphorescent light emitting materials has led to higher efficiency of devices. As phosphorescent materials, iridium complexes, platinum complexes, and the like are known (see, for example, Patent Document 1 and Patent Document 2), but no element has been developed that achieves both high efficiency and high durability.

In addition, organic EL elements using a compound having a sulfonyl group (SO ₂ ) as a material for high durability materials have been reported (for example, Non-Patent Document 1 and Non-Patent Document 2). However, the materials used for these materials have a small electron affinity (Ea), insufficient electron injection / transport to the light-emitting layer, high device driving voltage and power consumption, and low light emission efficiency. In addition, if it has a condensed ring or has a long conjugated system, the lowest excited triplet (T ₁ level) of the molecule is low, and phosphorescence from the phosphorescent material is quenched, resulting in low luminous efficiency. There's a problem.
US Pat. No. 6,303,238 International Publication No. 00/57676 Pamphlet “Journal of American Chemical Society, 2000, Vol. 122, pp. 19711-11978. “Advanced Functional Materials, 2005, Vol. 15, pp. 664-670.

  An object of the present invention is to provide an organic electroluminescence device having high luminous efficiency, high durability, and low voltage driving.

  As a result of studies to solve the above problems, the present inventors have found that an organic EL device containing a sulfoxide or sulfonyl 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 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 organic An organic electroluminescent device comprising a compound layer.

(In the general formula (I), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group, X ² represents a sulfinyl group or a sulfonyl group, R ¹ represents Represents a hydrogen atom or a substituent, and a plurality of R ¹ may be the same or different.)

  [2] The organic electroluminescent element 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), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group. X ² represents a sulfinyl group or a sulfonyl group. R ¹ represents Represents a hydrogen atom or a substituent, a plurality of R ¹ may be the same or different, m represents an integer of 2 or more, and L represents a single bond or an m-valent linking group.

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

(In the general formula (III), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group, X ² represents a sulfinyl group or a sulfonyl group, R ¹ represents Represents a hydrogen atom or a substituent, a plurality of R ¹ may be the same or different, R ³¹ represents a hydrogen atom or a substituent, a plurality of R ³¹ may be the same or different, m is 2 to 4 Represents an integer.)

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

(In the general formula (IV), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group. X ² represents a sulfinyl group or a sulfonyl group. R ¹ represents A hydrogen atom or a substituent, a plurality of R ¹ may be the same or different, Ar ⁴¹ represents an aromatic hydrocarbon ring or aromatic heterocycle, and R ⁴¹ represents a hydrogen atom or a substituent. ⁴¹ may be the same or different, m represents an integer of 2 or more, and n represents an integer of 1 or more.)

  [5] The glass transition temperature of the compound represented by the general formulas (I) to (IV) is 130 ° C. or higher and 450 ° C. or lower, and any one of the above [1] to [4] Organic electroluminescent device.

  [6] The lowest excited triplet energy level of the compounds represented by the general formulas (I) to (IV) is 65 kcal / mol (272.35 kJ / mol) or more and 95 kcal / mol (398.05 kJ / mol) or less. The organic electroluminescence device as described in any one of [1] to [5] above, wherein

[7] The organic electroluminescent element as described in any one of [1] to [6] above, wherein at least one of the light emitting materials is a phosphorescent light emitting material.

  [8] The organic electroluminescence device as described in [7] above, wherein the phosphorescent material is an iridium complex or a platinum complex.

[9] The organic electroluminescent element as described in any one of [1] to [8] above, wherein the light emitting layer contains compounds represented by the general formulas (I) to (IV).

[10] The electron transport layer according to [10], wherein the electron transport layer includes at least one electron transport layer between the light emitting layer and the cathode, and the compounds represented by the general formulas (I) to (IV) are contained in the electron transport layer. 1]-[9] The organic electroluminescent element in any one of.

  The organic electroluminescent device of the present invention (used in the present specification in the same meaning as the “device of the present invention”) is a compound represented by the general formulas (I) to (IV) of the present invention (hereinafter referred to as “the present invention”). In the organic compound layer. Thereby, it is possible to provide an organic electroluminescence device having high luminous efficiency, high durability and low voltage driving. In particular, by using a compound of the present invention having a specific structure (for example, exemplified compound 59) as a host material, it can be combined with a blue phosphorescent material having a large energy gap (T1) between the ground state and the lowest excited triplet state. In addition, it is possible to provide an element that is resistant to non-radiation deactivation and energy transfer, has high luminous efficiency, is highly durable and can be driven at a low voltage.

  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 1 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), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group, X ² represents a sulfinyl group or a sulfonyl group, R ¹ represents Represents a hydrogen atom or a substituent, and a plurality of R ¹ may be the same or different.)

The general formula (I) will be described. A ^{1 to} A ⁸ represent an N atom or CR ¹ , and R ¹ represents a hydrogen atom or a substituent. No particular limitation is imposed on the combination of A ¹ to A ^8, the number of N atoms is preferably 0-4 of A ¹ to A ^8, more preferably 0-2, 0 (A ¹ to A ⁸ All Is particularly preferred CR ¹ ). As the substituent represented by R ¹ , those exemplified 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 a sulfur atom, and specific examples include imidazolyl, pyridyl, quinolyl, furyl, thienyl, piperidyl, morpholino, benzoxazolyl, benzimidazolyl, benzthiazolyl, carbazolyl group, azepinyl group, and the like. Preferably they are C3-C40, More preferably, it is C3-C30, Most preferably, it is C3-C24, for example, trimethylsilyl, a triphenylsilyl etc. are mentioned, for example, A silyloxy group (Preferably C3-C3) 40, more preferably 3 to 30 carbon atoms, particularly preferably 3 to 24 carbon atoms, and examples thereof include trimethylsilyloxy and triphenylsilyloxy.

A plurality of R ¹ may be the same or different. In addition, R ¹ may further have a substituent, and those exemplified as the substituent group A can be applied as the substituent. In addition, R ¹ may be linked to each other to form a condensed ring. The formed ring includes a benzene ring, a pyridine ring, a pyrazine ring, a pyrimidine ring, a triazine ring, a pyridazine ring, a pyrrole ring, and a 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.

R ¹ is preferably a hydrogen atom, alkyl group, aryl group, fluorine group, amino group, alkoxy group, aryloxy group, heterocyclic oxy group, alkylthio group, arylthio group, heterocyclic thio group, cyano group, heterocyclic group , A silyl group and a silyloxy group, more preferably a hydrogen atom, an alkyl group, an aryl group, a fluorine group, a cyano group, a silyl group and a heterocyclic group, and particularly preferably a hydrogen atom, an alkyl group and an aryl group. .

X ¹ represents an S atom, a sulfinyl group or a sulfonyl group. X ² represents a sulfinyl group or a sulfonyl group. X ¹ is preferably an S atom or a sulfonyl group, more preferably a sulfonyl group, and X ² is preferably a sulfonyl group.

  One preferred form of the compound represented by the general formula (I) is a compound represented by the following general formula (II).

(In the general formula (II), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group. X ² represents a sulfinyl group or a sulfonyl group. R ¹ represents Represents a hydrogen atom or a substituent, a plurality of R ¹ may be the same or different, m represents an integer of 2 or more, and L represents a single bond or an m-valent linking group.

The general formula (II) will be described. ^{A 1 ~A 8, R 1,} X 1, and X ² is A ¹ to A ⁸ in formula ^{(I), R 1, X} 1, and X ² in the above formula, preferred ranges are also the same. m represents an integer of 2 or more. L represents a single bond or an m-valent linking group. Although it does not specifically limit as a coupling group, The coupling group comprised from 1 or more types of atoms selected from a carbon atom, a nitrogen atom, an oxygen atom, a sulfur atom, a silicon atom, a germanium atom, and a phosphorus atom is preferable. Specific examples of the linking group are shown below, but the present invention is not limited thereto.

L is more preferably a single bond, a substituted or unsubstituted carbon atom, a substituted or unsubstituted nitrogen atom, a substituted silicon atom, a substituted germanium atom, an oxygen atom, a sulfur atom, an aromatic hydrocarbon ring group, or an aromatic heterocyclic ring. More preferably a single bond, a substituted or unsubstituted carbon atom, a substituted or unsubstituted nitrogen atom, a substituted silicon atom, an aromatic hydrocarbon ring group, or an aromatic heterocyclic group, particularly preferably a substituted group. It is a silicon atom or an aromatic hydrocarbon ring group.
These linking groups may further have a substituent if possible, and the substituents that can be introduced include those listed as the substituent group A.

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

(In the general formula (III), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group, X ² represents a sulfinyl group or a sulfonyl group, R ¹ represents Represents a hydrogen atom or a substituent, a plurality of R ¹ may be the same or different, R ³¹ represents a hydrogen atom or a substituent, a plurality of R ³¹ may be the same or different, m is 2 to 4 Represents an integer.)

The general formula (III) will be described. ^{A 1 ~A 8, R 1,} X 1, and X ² is A ¹ to A ⁸ in formula ^{(I), R 1, X} 1, and X ² in the above formula, preferred ranges are also the same. R ³¹ represents a hydrogen atom or a substituent. As the substituent represented by R ³¹ , those exemplified as the substituent group A can be applied. R ³¹ is preferably a hydrogen atom, alkyl group, aryl group, amino group, alkoxy group, aryloxy group, heterocyclic oxy group, alkylthio group, arylthio group, heterocyclic thio group, cyano group, heterocyclic group, silyl group A silyloxy group, more preferably an alkyl group, an aryl group, an amino group, a cyano group or a heterocyclic group, still more preferably an alkyl group, an aryl group, a cyano group or a heterocyclic group, particularly preferably an alkyl group. Group, aryl group, and heterocyclic group. A plurality of R ³¹ may be the same or different.

(In the general formula (IV), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group. X ² represents a sulfinyl group or a sulfonyl group. R ¹ represents A hydrogen atom or a substituent, a plurality of R ¹ may be the same or different, Ar ⁴¹ represents an aromatic hydrocarbon ring or aromatic heterocycle, and R ⁴¹ represents a hydrogen atom or a substituent. ⁴¹ may be the same or different, m represents an integer of 2 or more, and n represents an integer of 1 or more.)

The general formula (IV) will be described. ^{A 1 ~A 8, R 1,} X 1, and X ² is A ¹ to A ⁸ in formula ^{(I), R 1, X} 1, and X ² in the above formula, preferred ranges are also the same. Ar ⁴¹ represents an aromatic hydrocarbon ring or an aromatic heterocycle, and R ⁴¹ represents a hydrogen atom or a substituent. As the substituent represented by R ⁴¹ , those exemplified as the substituent group A can be applied. R ⁴¹ is preferably a hydrogen atom, alkyl group, aryl group, fluorine group, amino group, alkoxy group, aryloxy group, heterocyclic oxy group, alkylthio group, arylthio group, heterocyclic thio group, cyano group, heterocyclic group , A silyl group and a silyloxy group, more preferably a hydrogen atom, an alkyl group, an aryl group, a fluorine group, a cyano group, a silyl group and a heterocyclic group, and particularly preferably a hydrogen atom, an alkyl group and an aryl group. . The plurality of R ⁴¹ may be the same or different.

The aromatic hydrocarbon ring or aromatic heterocycle represented by Ar ⁴¹ is not particularly limited, but a 4- to 10-membered ring is preferable, a 5- to 7-membered ring is more preferable, and 5- and 6-membered rings are more preferable. A member ring is particularly preferred. The heteroatom contained in the aromatic heterocycle represented by Ar ⁴¹ is not particularly limited, but an aromatic heterocycle containing nitrogen, oxygen, sulfur, selenium, silicon, germanium, and phosphorus is preferable, and nitrogen, oxygen, and sulfur are 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 ⁴¹ is not particularly limited, but is preferably 1 to 3.
Specific examples of the aromatic hydrocarbon ring or aromatic heterocycle represented by Ar ⁴¹ include a benzene ring, a pyridine ring, a pyrazine ring, a pyrimidine ring, a triazine ring, a pyridazine ring, a pyrrole ring, a pyrazole ring, an imidazole ring, and a triazole. And a 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 formed from Ar ⁴¹ 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 triazine. 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 aromatic hydrocarbon ring or aromatic heterocycle represented by Ar ⁴¹ is preferably a benzene ring, pyridine ring, pyrazine ring, pyrimidine ring, triazine ring, pyrrole ring, pyrazole ring, imidazole ring, triazole ring, oxazole ring, A thiazole ring, a furan ring and a thiophene ring, more preferably a benzene ring, a pyridine ring, a pyrazine ring, a pyrrole ring, a pyrazole ring, an imidazole ring, an oxazole ring, a thiazole ring and a thiophene ring, and more preferably a benzene ring. , A pyridine ring, a pyrazine ring, a pyrazole ring, an imidazole ring, and a thiophene ring, and particularly preferably a benzene ring, a pyridine ring, and a pyrazine ring.
m is an integer greater than or equal to 2, More preferably, it is 2-10, Most preferably, it is 2-6.

Specific examples of the compounds represented by the general formulas (I) to (IV) 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 (IV) of the present invention can be synthesized by various known synthesis methods. For example, Exemplary Compound 1 can be synthesized by the method described in The Journal of Physical Chemistry, 69, 2108-2111 (1965). For example, exemplary compound 59 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 compound of the present invention has a lowest excited triplet energy level (T1 level) of 65 kcal / mol (272.35 kJ / mol) or more and 95 kcal / mol (398.05 kJ / mol) or less is preferable, 67 kcal / mol (280.73 kJ / mol) or more, 95 kcal / mol (398.05 kJ / mol) or less is more preferable, and 68 kcal / mol (289.11 kJ / mol) or more. 95 kcal / mol (398.05 kJ / mol) or less is more preferable.

  Here, the T1 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 include yttria-stabilized zirconia (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 detailed in Yutaka Sawada's “New Development of Transparent Conductive Film” published by CMC (1999), 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 device of the present invention may be at least one organic compound layer including a light emitting layer between a pair of electrodes (a layer made of only an organic compound or an organic layer containing an inorganic compound). As described above, the organic compound layer other than the organic light emitting layer includes, for example, a hole transport layer, an electron transport layer, a charge blocking layer, a hole injection layer, and an electron injection layer. Can be mentioned.

-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, bisstyrylanthracene derivatives, quinacridone derivatives, pyrrolopyridine derivatives, thiadiazolopyridine derivatives, cyclopentadiene derivatives, styrylamine derivatives, di Various gold typified by ketopyrrolopyrrole derivatives, aromatic dimethylidin compounds, metal complexes of 8-quinolinol derivatives and metal complexes of pyromethene derivatives Complexes, 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 a carbazole derivative, a triazole derivative, an oxazole derivative, an oxadiazole derivative, an imidazole derivative, a polyarylalkane derivative, a pyrazoline derivative, and a pyrazolone derivative in addition to the compound of the present invention. , Phenylenediamine derivatives, arylamine derivatives, amino-substituted chalcone derivatives, styrylanthracene derivatives, fluorenone derivatives, hydrazone derivatives, stilbene derivatives, silazane derivatives, aromatic tertiary amine compounds, styrylamine compounds, aromatic dimethylidin compounds, porphyrins A layer containing a compound, an organic silane derivative, carbon, or the like is 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 compounds of the present invention, aluminum complexes such as BAlq, triazole derivatives, phenanthroline derivatives such as BCP, and the like.
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 SiNx and SiNxOy, metal fluorides such as MgF ₂ , LiF, AlF ₃ and CaF ₂ , polyethylene, polypropylene, polymethyl methacrylate, polyimide, Copolymerizing polyurea, polytetrafluoroethylene, polychlorotrifluoroethylene, polydichlorodifluoroethylene, a copolymer of chlorotrifluoroethylene and dichlorodifluoroethylene, and a monomer mixture containing tetrafluoroethylene and at least one comonomer. Copolymer, fluorine-containing copolymer having a cyclic structure in the copolymer main chain Examples thereof include a polymer, a water-absorbing substance having a water absorption of 1% or more, and a moisture-proof substance having a water absorption of 0.1% or less.

  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.

(Hole transport layer)
NPD: film thickness 40nm
(Light emitting layer)
mCP = 90 mass%, Ferric = 10 mass%: film thickness 50 nm
(Electron transport layer)
BAlq: film thickness 40 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>
An organic electroluminescent device of Comparative Example 2 was produced in the same manner as the organic electroluminescent device of <Comparative Example 1> except that the light emitting layer was changed to the following layer.

(Light emitting layer)
mCP = 89% by mass, compound (V) [Non-patent document 2 “Compound described in Advanced Functional Materials, 2005, Vol. 15, p.664-670” = 1 mass %, Ferric = 10 mass%: film thickness 50 nm

  The chemical structures of NPD, CBP, Firpic, BAlq and compound (V) 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 the light emitting layer was changed to the layer described below.

(Light emitting layer)
mCP = 89% by mass, exemplary compound 59 = 1% by mass, Ferric = 10% by mass: film thickness 50 nm

The elements of Example 1, Comparative Example 1 and Comparative Example 2 were set in an OLED test system ST-D type manufactured by Tokyo System Development Co., Ltd. and driven at a current density of 10 mA / cm ² . In Example 1 and Comparative Example 1, blue light emission of λmax = 467 and 468 nm was obtained, respectively. On the other hand, in the device of Comparative Example 2, no light emission derived from Ferpic was observed. The applied voltages when the elements of Example 1 and Comparative Example 1 were driven at 10 mA / cm ² were compared. While the applied voltage of the device of Comparative Example 1 was 15V, the device of Example 1 achieved 12V with a voltage of 12V. Moreover, T1 value of exemplary compound (59) was 68.26 kcal / mol.

<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 the electron transport layer was changed to the layer described below. The first electron transport material layer is located on the light emitting layer side.

(First electron transport layer)
BAlq: film thickness 30 nm
(Second electron transport layer)
Illustrative compound 59: film thickness: 10 nm,

The applied voltages when the devices of Comparative Example 2 and Example 2 were driven at 1 mA / cm ² were compared. While the applied voltage of the device of Comparative Example 2 was 12V, the device of Example 2 was 11V, and a voltage reduction of 1V was realized.

  As is clear from the above examples, it was found that the driving voltage of the organic electroluminescence device can be lowered by using the compound of the present invention.

Claims (10)

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 formed in the organic compound layer An organic electroluminescent element characterized by containing.

(In the general formula (I), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group, X ² represents a sulfinyl group or a sulfonyl group, R ¹ represents Represents a hydrogen atom or a substituent, and a plurality of R ¹ may be the same or different.) 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), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group. X ² represents a sulfinyl group or a sulfonyl group. R ¹ represents Represents a hydrogen atom or a substituent, a plurality of R ¹ may be the same or different, m represents an integer of 2 or more, and L represents a single bond or an m-valent linking group. The organic electroluminescent device according to claim 2, wherein the compound represented by the general formula (II) is represented by the following general formula (III).

(In the general formula (III), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group, X ² represents a sulfinyl group or a sulfonyl group, R ¹ represents Represents a hydrogen atom or a substituent, a plurality of R ¹ may be the same or different, R ³¹ represents a hydrogen atom or a substituent, a plurality of R ³¹ may be the same or different, m is 2 to 4 Represents an integer.) The organic electroluminescent device according to claim 2, wherein the compound represented by the general formula (II) is represented by the following general formula (IV).

(In the general formula (IV), A ^{1 to} A ⁸ represent an N atom or CR ¹ , X ¹ represents an S atom, a sulfinyl group or a sulfonyl group. X ² represents a sulfinyl group or a sulfonyl group. R ¹ represents A hydrogen atom or a substituent, a plurality of R ¹ may be the same or different, Ar ⁴¹ represents an aromatic hydrocarbon ring or aromatic heterocycle, and R ⁴¹ represents a hydrogen atom or a substituent. ⁴¹ may be the same or different, m represents an integer of 2 or more, and n represents an integer of 1 or more.)   The organic electroluminescent element according to any one of claims 1 to 4, wherein the compounds represented by the general formulas (I) to (IV) 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 (IV) 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 5, wherein   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 electroluminescence device according to claim 7, wherein the phosphorescent material is an iridium complex or a platinum complex.   The organic electroluminescent element according to any one of claims 1 to 8, wherein the compound represented by the general formulas (I) to (IV) is contained in the light emitting layer.   10. The electron transporting layer comprising at least one electron transporting layer between the light emitting layer and the cathode and containing the compounds represented by the general formulas (I) to (IV) in the electron transporting layer. The organic electroluminescent element according to any one of the above.