JPWO2006126389A1 - ORGANIC ELECTROLUMINESCENT ELEMENT MATERIAL, ORGANIC ELECTROLUMINESCENT ELEMENT, DISPLAY DEVICE AND LIGHTING DEVICE - Google Patents

Abstract

The present invention provides an organic EL device material having a controlled emission wavelength, high emission efficiency, and a long emission lifetime. This organic EL element material is a metal complex having the following general formula (1) or a tautomer thereof as a partial structure. [Chemical 1]

Description

  The present invention relates to an organic electroluminescence element material, an organic electroluminescence element, a display device, and a lighting device.

  Conventionally, as a light-emitting electronic display device, there is an electroluminescence display (hereinafter referred to as ELD). Examples of constituent elements of ELD include inorganic electroluminescent elements and organic electroluminescent elements (hereinafter referred to as organic EL elements). Inorganic electroluminescent elements have been used as planar light sources, but an alternating high voltage is required to drive the light emitting elements. An organic EL device has a structure in which a light emitting layer containing a compound that emits light is sandwiched between a cathode and an anode, and injects electrons and holes into the light emitting layer and recombines them to generate excitons. An element that emits light by using light emission (fluorescence / phosphorescence) when this exciton is deactivated, and can emit light at a voltage of several V to several tens V, and is self-luminous. Therefore, it has a wide viewing angle, high visibility, and since it is a thin-film type complete solid-state device, it has attracted attention from the viewpoints of space saving and portability.

  However, in organic EL elements for practical use in the future, development of organic EL elements that emit light efficiently and with high luminance with lower power consumption is desired.

  In Japanese Patent No. 3093796, a small amount of phosphor is doped into a stilbene derivative, a bisstyrylarylene derivative or a tristyrylarylene derivative to achieve improvement in light emission luminance and a longer lifetime of the device.

  Further, an element having an organic light-emitting layer in which an 8-hydroxyquinoline aluminum complex is used as a host compound and a small amount of phosphor is doped thereto (for example, JP-A 63-264692), and an 8-hydroxyquinoline aluminum complex is used as a host compound. For example, an element having an organic light emitting layer doped with a quinacridone dye (for example, JP-A-3-255190) is known.

  As described above, when light emission from excited singlet is used, the generation ratio of singlet excitons and triplet excitons is 1: 3, and thus the generation probability of luminescent excited species is 25%. Since the efficiency is about 20%, the limit of the external extraction quantum efficiency (ηext) is set to 5%.

  However, since Princeton University reported on organic EL devices using phosphorescence emission from excited triplets (MA Baldo et al., Nature, 395, 151-154 (1998)), at room temperature. Research on materials that exhibit phosphorescence has become active.

  For example, M.M. A. Baldo et al. , Nature, 403, 17, 750-753 (2000), US Pat. No. 6,097,147, and the like.

  When excited triplets are used, the upper limit of internal quantum efficiency is 100%, so that in principle the luminous efficiency is four times that of excited singlets, and there is a possibility that almost the same performance as cold cathode tubes can be obtained. Therefore, it is attracting attention as a lighting application.

  For example, S.M. Lamansky et al. , J .; Am. Chem. Soc. , 123, 4304 (2001), etc., many compounds have been studied for synthesis centering on heavy metal complexes such as iridium complexes.

  In addition, the aforementioned M.I. A. Baldo et al. , Nature, Vol. 403, No. 17, pages 750-753 (2000), studies have been made using tris (2-phenylpyridine) iridium as a dopant.

In addition, M.M. E. Thompson et al., In The 10th International Works on Inorganic and Organic Electroluminescence (EL'00, Hamamatsu), used L ₂ Ir (acac), for example, (ppy) ₂ Ir (acac) as a dopant, J
Youn. 0 g, Tetsuo Tsutsui, etc., again, The 10th International Workshop on Inorganic and Organic Electroluminescence (EL'00, Hamamatsu) in, as a dopant tris (2-(p-tolyl) pyridine) iridium (Ir (ptpy) _3), Studies using tris (benzo [h] quinoline) iridium (Ir (bzq) ₃ ) and the like are being conducted (note that these metal complexes are generally called ortho-metalated iridium complexes).

  In addition, S. Lamansky et al. , J .; Am. Chem. Soc. , 123, 4304 (2001), etc., attempts have been made to form devices using various iridium complexes.

  In order to obtain high luminous efficiency, in the 10th International Works on Inorganic and Organic Electroluminescence (EL'00, Hamamatsu), Ikai et al. Uses a hole transporting compound as a host of a phosphorescent compound. In addition, M.M. E. Thompson et al. Use various electron transporting materials as a host of a phosphorescent compound, doped with a novel iridium complex.

  Orthometalated complexes in which the central metal is platinum instead of iridium are also attracting attention. With respect to this type of complex, many examples in which a ligand is characterized are known (see, for example, Patent Documents 1 to 5 and Non-Patent Document 1).

  In any case, the light emission luminance and light emission efficiency of the light emitting device are greatly improved compared to conventional devices because the emitted light is derived from phosphorescence. There is a problem that it is lower than the conventional element.

On the other hand, in order to realize a blue emission wavelength, an electron-withdrawing group such as a fluorine atom, a trifluoromethyl group or a cyano group has been introduced into phenylpyridine or phenylpyrazole as a substituent, and picolinic acid as a ligand. And pyrazabole-based ligands are known to be introduced (for example, see Patent Documents 6 to 14 and Non-Patent Documents 1 to 4). With these ligands, the emission wavelength of the light-emitting material is shortened. While blue can be achieved and a high-efficiency device can be achieved, the light emission lifetime of the device is greatly deteriorated, and thus an improvement in the trade-off has been required.
JP 2002-332291 A JP 2002-332292 A JP 2002-338588 A JP 2002-226495 A JP 2002-234894 A International Publication No. 02/15645 Pamphlet JP 2003-123982 A JP 2002-117978 A JP 2003-146996 A International Publication No. 04/016711 Pamphlet International Publication No. 04/085450 Pamphlet International Publication No. 05/003095 Pamphlet International Publication No. 05/007767 Pamphlet International Publication No. 04/101707 Pamphlet Inorganic Chemistry, Vol. 41, No. 12, pp. 3055-3066 (2002) Applied Physics Letters, Volume 79, 2082 (2001) Applied Physics Letters, 83, 3818 (2003) New Journal of Chemistry, 26, 1171 (2002)

  The present invention has been made in view of the above problems, and an object of the present invention is to provide an organic EL element material having a controlled emission wavelength, high emission efficiency, and a long emission lifetime, and an organic EL element using the same An illumination device and a display device are provided.

  The above object of the present invention has been achieved by the following constitutions 1 to 13.

  (1) An organic electroluminescence device material, which is a metal complex having the following general formula (1) or a tautomer thereof as a partial structure.

(In the formula, R ₁₁ , R ₁₂ , R ₁₃ , R ₁₄ , R ₁₅ each represents a hydrogen atom or a substituent, X ₀₁ , X ₀₂ , X ₀₃ , X ₀₄ each represents a carbon atom or a nitrogen atom; ₀₁ represents a group 8-10 metal in the periodic table, a bond between X ₀₁ and N, a bond between N and X _04, a bond between X ₀₄ and X ₀₃ , a bond between X ₀₃ and X ₀₂ , X ₀₂ And X ₀₁ each represents an end bond or a double bond, and u2 represents an integer of 0 to 3, provided that at least two of R _{11 to} R ₁₄ are aromatic groups, or R ₁₁ to At least one of R ₁₄ is an electron-withdrawing group and R ₁₅ is an aromatic group, or at least two of R _{11 to} R _{14 are-} (Ar ₀ ) _u0- (X) _a0- ( R ₀₎ is a group represented by _u1. here, Ar ₀ is Represents an aromatic group, X represents an oxygen atom, a sulfur atom or a nitrogen atom, R ₀ represents a substituent, u0 and a0 are both 0 or 1, u1 represents 1 or 2. However, u0 and a0 is not 0 at all.)
(2) The organic electroluminescent element material as described in (1) above, which is a metal complex having the following general formula (1A) or a tautomer thereof as a partial structure.

(In the formula, R _b represents a hydrogen atom or a substituent. X ₁₁ represents a carbon atom or a nitrogen atom. X ₁₂ , X ₁₃ and X ₁₄ represent CR _c , a nitrogen atom or NR _d . R _c , R _d represents a hydrogen atom or a substituent, ma and mb represent an integer satisfying 2 ≦ ma ≦ 4 and ma + mb = 4, Ar ₀₀ represents an aromatic carbocyclic group or an aromatic heterocyclic group, and M ₁₁ represents an element. Represents a group 8-10 metal in the periodic table, a bond between X ₁₁ and N, a bond between N and X ₁₄ , a bond between X ₁₄ and X ₁₃ , a bond between X ₁₃ and X ₁₂ , X ₁₂ and X The bond to ₁₁ represents a single bond or a double bond, respectively.)
(3) The organic electroluminescent element material as described in (1) above, which is a metal complex having the following general formula (2) or a tautomer thereof as a partial structure.

(In the formula, R _e , R _f , R ₂₁ and R ₂₂ represent a hydrogen atom or a substituent. X ₂₁ represents a carbon atom or a nitrogen atom. X ₂₂ , X ₂₃ and X ₂₄ represent CR _g , a nitrogen atom or NR _h represents R _g and R _h each represents a hydrogen atom or a substituent, nb and nc represent 1 or 2, n1 and n2 represent 0 or ₁ , Ar ₁ and Ar ₂ represent aromatic carbocyclic groups Or an aromatic heterocyclic group, X _b and X _{c each} represents an oxygen atom, a sulfur atom or a nitrogen atom, and M ₂₁ represents a group 8-10 metal in the periodic table of the elements between X ₂₁ and N A bond, a bond between N and X ₂₄ , a bond between X ₂₄ and X ₂₃ , a bond between X ₂₃ and X ₂₂ and a bond between X ₂₂ and X ₂₁ are each a single bond or Represents a double bond.)
(4) The organic electroluminescent element material as described in (1) above, which is a metal complex having the following general formula (3) or a tautomer thereof as a partial structure.

(In the formula, R ₃₁ , R ₃₂ , R ₃₃ and R ₃₄ represent a hydrogen atom or a substituent, but at least one represents an electron-withdrawing group. X ₃₅ represents a carbon atom or a nitrogen atom. X ₃₆ , X ₃₇ and X ₃₈ represent CR ₃₅ , a nitrogen atom or NR ₃₆ , at least one of which is CR _35. R ₃₅ and R ₃₆ each represents a hydrogen atom or a substituent, and at least one of R ₃₅ is aromatic. M ₃₁ represents a group 8-10 metal in the periodic table, a bond between X ₃₅ and N, a bond between N and X ₃₈ , X ₃₈ and X ₃₇ And the bond between X ₃₇ and X ₃₆ and the bond between X ₃₆ and X ₃₅ each represent a single bond or a double bond.)
(5) The organic electroluminescent element material as described in (1) above, which is a metal complex having the following general formula (4) or a tautomer thereof as a partial structure.

(In the formula, R ₄₁ , R ₄₂ , R ₄₃ and R ₄₄ represent a hydrogen atom or a substituent, but at least one of R ₄₁ and R ₄₂ represents an electron-withdrawing group. X ₄₅ represents a carbon atom or a nitrogen atom. X ₄₆ , X ₄₇ and X ₄₈ represent CR ₄₅ , a nitrogen atom or NR ₄₆ , at least one of which is CR _45. R ₄₅ and R ₄₆ represent a hydrogen atom or a substituent R ₄₅ At least one of them represents an aromatic carbocyclic group or an aromatic heterocyclic group, M ₄₁ represents a group 8-10 metal in the periodic table, a bond between X ₄₅ and N, a bond between N and X ₄₈ , X ₄₈ and X ₄₇ , X ₄₇ and X _46, and X ₄₆ and X ₄₅ each represent a single bond or a double bond.)
(6) The organic electroluminescent element material as described in (1) above, wherein M ₀₁ is iridium or platinum.

  (7) An organic electroluminescence element comprising the organic electroluminescence element material according to (1).

  (8) An organic electroluminescent element having a light emitting layer as a constituent layer, wherein the light emitting layer has the organic electroluminescent element material described in (1) above.

  (9) An organic electroluminescence device having an electron blocking layer as a constituent layer, wherein the electron blocking layer contains the organic electroluminescence device material described in (1) above.

  (10) An organic electroluminescence device having a light emitting layer as a constituent layer, wherein at least one of carbon atoms of a carboline derivative or a hydrocarbon ring constituting a carboline ring of the carboline derivative is substituted with a nitrogen atom. The organic electroluminescent device according to (7) above, comprising a derivative having a cyclic structure.

  (11) An organic electroluminescence device having a hole blocking layer as a constituent layer, wherein the hole blocking layer is a carboline derivative or at least one of carbon atoms of a hydrocarbon ring constituting a carboline ring of the carboline derivative is nitrogen The organic electroluminescent device according to (7) above, which contains a derivative having a ring structure substituted with an atom.

  (12) A display device comprising the organic electroluminescence element according to (7).

  (13) An illuminating device comprising the organic electroluminescence element according to (7).

  According to the present invention, an organic EL element material useful for an organic EL element can be obtained. By using the organic EL element material, the emission wavelength is controlled, the organic EL element exhibits high luminous efficiency, and has a long emission lifetime. An illumination device and a display device can be provided.

It is the schematic diagram which showed an example of the display apparatus comprised from an organic EL element. 4 is a schematic diagram of a display unit A. FIG. It is an equivalent circuit diagram of the drive circuit which comprises a pixel. It is a schematic diagram of the display apparatus by a passive matrix system. It is a schematic diagram of the sealing structure of an organic EL element. It is a schematic diagram of the illuminating device which comprises an organic EL element.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Display 3 Pixel 5 Scan line 6 Data line 7 Power supply line 10 Organic EL element 11 Switching transistor 12 Drive transistor 13 Capacitor A Display part B Control part 101 Glass substrate with a transparent electrode 102 Organic EL layer 103 Cathode 104 Glass sealing can 105 Barium oxide (water trapping agent)
106 Nitrogen gas 107 UV curable adhesive

  As a result of intensive studies on the above problems, the present inventors have found that a benzene ring typified by phenylpyrazole or phenylimidazole used as a ligand of a metal complex and a five-membered heterocycle are linked and bonded. It has been found that the light emission lifetime, which has been a problem in the prior art, is greatly improved by a metal complex in which the following substituents are introduced at specific positions of the ring serving as the parent nucleus of the ligand. (1) A metal complex in which two or more aromatic carbocycles which may have a substituent or aromatic heterocycles which may have a substituent are introduced as substituents on a benzene ring. (2) A metal complex introduced as a substituent in a form in which the substituent on the benzene ring is represented by the general formula (2). (3) When an electron-withdrawing group is substituted on the benzene ring, an aromatic carbocycle which may have at least one substituent or a substituent on the five-membered heterocyclic ring A metal complex in which one or more good aromatic heterocycles are introduced as a substituent.

  By using an organic EL element including such an organic EL element material, the emission wavelength is shortened, and the emission wavelength is controlled to the short wavelength side only by a conventional blue metal complex, particularly an electron withdrawing group. We found that it is possible to design the phosphorescent blue light-emitting dopant from a different viewpoint from that produced using device materials, and that the short emission life that was a problem of organic EL devices was greatly reduced. I found it to be improved.

  In addition, by using such an organic EL element material, it was possible to provide an organic EL element, a lighting device, and a display device that exhibit high light emission efficiency and have a long light emission lifetime.

  In this study, we used the following structure as an example to simulate the emission wavelength by molecular orbital calculation, and to examine the details of the substituent effect on the ligand in which the benzene ring and the five-membered heterocycle are linked and bonded, and the fluctuation of the emission wavelength. It was examined.

(In the formula, n represents an integer of 2 or 3. X ₁₁ represents a carbon atom or a nitrogen atom. X ₁₂ , X ₁₃ and X ₁₄ represent CR _c , a nitrogen atom or NR _d . R _c and R _d Represents a hydrogen atom or a substituent, M ₁₁ represents a group 8-10 metal in the periodic table, a bond between X ₁₁ and N, a bond between N and X ₁₄ , a bond between X ₁₄ and X ₁₃ , The bond between X ₁₃ and X ₁₂ and the bond between X ₁₂ and X ₁₁ each represents a single bond or a double bond.)
For the calculation of the emission wavelength, Gaussian 98 (Revision A.11.4, MJ Frisch, GW Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, V. G. Zakrzewski, JA Montgomery, Jr., RE Stratmann, J. C. Burrant, S. Daprich, J. M. Millam, AD Daniels, K.N. Kudin, M. C. Strain, O. Farkas, J. Tomasi, V. Barone, M. Cossi, R. Cammi, B. Mennucci, C. Pomeri, C. Adamo, S. Clifford, J. Ochterski, G. A. Petersson, P.A. Ayala, Q. Cui, K. Morokuma, N. Rega, P. Salvador, J. J. Dannenberg, D. K. Malick, A. D. Rabuck, K. Ragavachari, J. B. Foresman, J. Cioslowsk , JV Ortiz, AG Baboul, BB Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R. Gomperts, RL Martin, D. J. Fox. , T. Keith, MA Al-Laham, CY Peng, A. Nanayakara, M. Challacombe, PM GW Gill, B. Johnson, W. Chen, MW Wong, J L. Andres, C. Go nzalez, M. Head-Gordon, ES Replogle, and JA Popple, Gaussian, Inc., Pittsburgh PA, 2002.).

  The calculation method was TD-DFT calculation by the B3LYP method.

  As a result, regarding the shortening of the wavelength, when the substituent is an electron donating group, introduction of the substituent at the 4p position and the 6p position is effective, whereas when the substituent is an electron withdrawing group, the 3p position, 5p position is effective. It was found that introduction of a substituent at the position was effective.

  In response to this result, the present inventors proceeded with studies based on the above guidelines as a means for shortening the emission wavelength to blue, synthesized it, and studied it, and it was possible to control the emission wavelength almost satisfying the simulation results. I found.

  However, it has been found that the introduction of an electron withdrawing group at the 3p position and the 5p position is effective in improving the blue color purity, while the lifetime of the device is significantly deteriorated. When an aromatic carbocyclic ring which may have a substituent or an aromatic heterocyclic ring which may have a substituent is introduced as a substituent, it has been found that this is improved.

  Preferred substituents on the ring serving as the parent nucleus of the ligand in which the benzene ring and the 5-membered heterocycle of the present invention are linked and bonded include an aromatic carbocycle, an aromatic heterocycle, an alkoxy group, an alkylthio group, An alkylamino group is mentioned.

  Based on such knowledge, the molecular structure represented by claims 1 to 6 of the present invention has been reached, and the present invention has been achieved.

  Further, as the inclusion layer in the element of the metal complex, a light emitting layer and / or an electron blocking layer is preferable. When the element is contained in the light emitting layer, it is used as a light emitting dopant in the light emitting layer. As a result, it was possible to achieve a long emission lifetime of the organic EL element.

  Hereinafter, details of each component according to the present invention will be sequentially described.

  The metal complex which is the organic EL element material of the present invention will be described.

  The light emitting layer and / or the hole blocking layer may be used as the metal complex containing layer having the general formula (1), (1A), (2) to (4) or a tautomer thereof as a partial structure according to the present invention. In addition, when it is contained in the light emitting layer, it can be used as a light emitting dopant in the light emitting layer to increase the efficiency of external extraction quantum efficiency of the organic EL device of the present invention (higher brightness) and to extend the light emitting lifetime. Can be achieved.

<< Metal Complex Having General Formula (1) or its Tautomer as Partial Structure >>
A metal complex having the general formula (1) or a tautomer thereof according to the present invention as a partial structure (hereinafter also referred to as a metal complex represented by the general formula (1)) will be described.

In General formula (1), R < ₁₁ > -R < ₁₅ > represents a hydrogen atom or a substituent. Examples of the substituent represented by R _{11 to} R ₁₅ include an alkyl group (for example, methyl group, ethyl group, isopropyl group, hydroxyethyl group, methoxymethyl group, trifluoromethyl group, t-butyl group), cycloalkyl. Group (for example, cyclopentyl group, cyclohexyl group, etc.), aralkyl group (for example, benzyl group, 2-phenethyl group, etc.), aromatic hydrocarbon group (for example, phenyl group, p-chlorophenyl group, mesityl group, tolyl group, xylyl group) Group, biphenylyl group, naphthyl group, anthryl group, phenanthryl group, etc.), aromatic heterocyclic group (for example, furyl group, thienyl group, pyridyl group, pyridazinyl group, pyrimidinyl group, pyrazinyl group, triazinyl group, imidazolyl group, pyrazolyl group) , Thiazolyl group, quinazolinyl group, carbazolyl group, phthalazinyl group ), Alkoxyl groups (for example, ethoxy group, isopropoxy group, butoxy group, etc.), aryloxy groups (for example, phenoxy group, naphthyloxy group, etc.), cyano groups, hydroxyl groups, alkenyl groups (for example, vinyl group), styryl Group, halogen atom (for example, chlorine atom, bromine atom, iodine atom, fluorine atom, etc.) and the like. These groups may be further substituted.

X ₀₁ , X ₀₂ , X ₀₃ and X ₀₄ each represent a carbon atom or a nitrogen atom, M ₀₁ represents a group 8-10 metal in the periodic table, and M ₀₁ is preferably iridium or platinum. In addition, the bond between X ₀₁ and N, the bond between N and X ₀₄ , the bond between X ₀₄ and X ₀₃ , the bond between X ₀₃ and X _02, and the bond between X ₀₂ and X ₀₁ are each an end bond or two bonds. Represents a double bond, and u2 represents an integer of 0 to 3. Provided that at least two of R _{11 to} R ₁₄ are aromatic groups, at least one of R _{11 to} R ₁₄ is an electron-withdrawing group, and R ₁₅ is an aromatic group, or R at least two ₁₁ to R _{14 is, - (Ar 0) u0 -} (X) a0 - (R 0) is a group represented by _u1. Here, Ar ₀ represents an aromatic group, X represents an oxygen atom, a sulfur atom or a nitrogen atom, R ₀ represents a substituent, u0 and a0 both represent 0 or 1, u ₁ represents 1 or 2 Represents. However, u0 and a0 are not both 0.

The aromatic group in the case where at least two of R _{11 to} R ₁₄ are aromatic groups, and the aromatic group represented by Ar ₀ represent an aromatic carbocyclic group or an aromatic heterocyclic group. As the aromatic carbocyclic group, benzene ring, biphenyl ring, naphthalene ring, azulene ring, anthracene ring, phenanthrene ring, pyrene ring, chrysene ring, naphthacene ring, triphenylene ring, o-terphenyl ring, m-terphenyl ring, Examples thereof include a p-terphenyl ring, an acenaphthene ring, a coronene ring, a fluorene ring, a fluoranthrene ring, a naphthacene ring, a pentacene ring, a perylene ring, a pentaphen ring, a picene ring, a pyrene ring, a pyranthrene ring, and an anthrathrene ring.

  The aromatic heterocyclic group includes furan ring, thiophene ring, pyridine ring, pyridazine ring, pyrimidine ring, pyrazine ring, triazine ring, benzimidazole ring, oxadiazole ring, triazole ring, imidazole ring, pyrazole ring, thiazole. Ring, indole ring, benzimidazole ring, benzothiazole ring, benzoxazole ring, quinoxaline ring, quinazoline ring, phthalazine ring, carbazole ring, carboline ring, diazacarbazole ring (one of the carbon atoms of the hydrocarbon ring constituting the carboline ring) One of which represents a ring further substituted with a nitrogen atom).

As the substituent represented by _{R 0,} which is synonymous with the substituents represented by _R 11 _{to R 15.}

When at least one of R _{11 to} R ₁₄ is an electron-withdrawing group, the electron-withdrawing group refers to a group having a Hammett's substituent constant σp exceeding 0. Hammett's σp value is a substituent constant determined by Hammett et al. From the electronic effect of the substituent on the hydrolysis of ethyl benzoate. “Structure-activity relationship of drugs” (Nanedo: 1979), “Substituent” The groups described in “Constants for Correlation Analysis in chemistry and biology” (C. Hansch and A. Leo, John Wiley & Sons, New York, 1979) can be cited.

In the present invention, σp of the electron withdrawing group is preferably 0.10 or more. Examples of the electron withdrawing group having σp of 0.10 or more include -B (OH) ₂ (0.12), bromine atom (0.23), chlorine atom (0.23), iodine atom (0.18). _{), - CBr 3 (-0.29)} , - CCl 3 (0.33), - CCF 3 (0.54), - CN (0.66), - CHO (0.42), - COOH (0 .45), CONH ₂ (0.36), —CH ₂ SO ₂ CF ₃ (0.31), —COCH ₃ (0.45), 3-valenyl group (0.19), —CF (CF ₃ ). ₂ (0.53), —CO ₂ C ₂ H ₅ (0.45), —CF ₂ CF ₂ CF ₂ CF ₃ (0.52), —C ₆ F ₅ (0.41), 2-benzoxa Zoriru group (0.33), 2-benzothiadiazolyl no doubt Lil group (0.29), - C = O (C 6 H 5) (0.43), - OCF 3 (0.35), - OSO 2 _{H 3 (0.36), - SO} 2 (NH 2) (0.57), - SO 2 CH 3 (0.72), - COCH 2 CH 3 (0.48), - COCH (CH 3) 2 (0.47), —COC (CH ₃ ) ₃ (0.32) and the like can be mentioned, but the present invention is not limited to these.

<< Metal Complex Having General Formula (1A) or its Tautomer as Partial Structure >>
A metal complex having the general formula (1) or a tautomer thereof according to the present invention as a partial structure (hereinafter, also referred to as a metal complex represented by the general formula (1A)) will be described.

In the general formula (1A), R _b represents a hydrogen atom or a substituent. Examples of the substituent represented by R _b include an alkyl group (for example, a methyl group, an ethyl group, an isopropyl group, a hydroxyethyl group, a methoxymethyl group, a trifluoromethyl group, a t-butyl group), a cycloalkyl group (for example, , Cyclopentyl group, cyclohexyl group, etc.), aralkyl group (for example, benzyl group, 2-phenethyl group, etc.), aromatic hydrocarbon group (for example, phenyl group, p-chlorophenyl group, mesityl group, tolyl group, xylyl group, biphenylyl). Group, naphthyl group, anthryl group, phenanthryl group, etc.), aromatic heterocyclic group (for example, furyl group, thienyl group, pyridyl group, pyridazinyl group, pyrimidinyl group, pyrazinyl group, triazinyl group, imidazolyl group, pyrazolyl group, thiazolyl group) Quinazolinyl group, carbazolyl group, phthalazinyl group, etc.), alcohol Sil group (for example, ethoxy group, isopropoxy group, butoxy group, etc.), aryloxy group (for example, phenoxy group, naphthyloxy group, etc.), cyano group, hydroxyl group, alkenyl group (for example, vinyl group, etc.), styryl group, Halogen atoms (for example, chlorine atom, bromine atom, iodine atom, fluorine atom, etc.) and the like can be mentioned. These groups may be further substituted.

X ₁₁ represents a carbon atom or a nitrogen atom.

X ₁₂ , X ₁₃ and X _{14 each} represent CR _c , a nitrogen atom or NR _d . R _c and R _d represent a hydrogen atom or a substituent. The substituent represented by R _c and R _d has the same meaning as the substituent represented by R _b .

  ma and mb represent integers satisfying 2 ≦ ma ≦ 4 and ma + mb = 4.

Ar ₀₀ represents an aromatic carbocyclic group or an aromatic heterocyclic group. As the aromatic carbocyclic group, benzene ring, biphenyl ring, naphthalene ring, azulene ring, anthracene ring, phenanthrene ring, pyrene ring, chrysene ring, naphthacene ring, triphenylene ring, o-terphenyl ring, m-terphenyl ring, Examples thereof include a p-terphenyl ring, an acenaphthene ring, a coronene ring, a fluorene ring, a fluoranthrene ring, a naphthacene ring, a pentacene ring, a perylene ring, a pentaphen ring, a picene ring, a pyrene ring, a pyranthrene ring, and an anthrathrene ring.

Examples of the aromatic heterocyclic group represented by Ar ₀₀ include a furan ring, a thiophene ring, a pyridine ring, a pyridazine ring, a pyrimidine ring, a pyrazine ring, a triazine ring, a benzimidazole ring, an oxadiazole ring, a triazole ring, an imidazole ring, Pyrazole ring, thiazole ring, indole ring, benzimidazole ring, benzothiazole ring, benzoxazole ring, quinoxaline ring, quinazoline ring, phthalazine ring, carbazole ring, carboline ring, diazacarbazole ring (the hydrocarbon ring constituting the carboline ring) A ring in which one of the carbon atoms is further substituted with a nitrogen atom).

M ₁₁ represents a group 8-10 metal in the periodic table. M ₁₁ is preferably iridium or platinum.

The bond between X ₁₁ and N, the bond between N and X ₁₄ , the bond between X ₁₄ and X ₁₃ , the bond between X ₁₃ and X _12, and the bond between X ₁₂ and X ₁₁ are each a single bond or a double bond Represents a bond.

In the general formula (1A), Ar ₀₀ is preferably represented by the following general formula (1-1).

Formula _{(1-1) -Ar 01 - (X} ) a - (R a) na
In General Formula (1-1), Ar ₀₁ represents an aromatic carbocyclic group or an aromatic heterocyclic group. The aromatic carbocyclic group or aromatic heterocyclic group represented by Ar ₀₁ has the same meaning as the aromatic carbocyclic group or aromatic heterocyclic group represented by Ar ₀₀ .

  X represents an oxygen atom, a sulfur atom or a nitrogen atom.

R _a represents a hydrogen atom or a substituent. The substituent represented by R _a has the same meaning as the substituent represented by R _b .

  na represents 1 or 2, and a represents 0 or 1.

<< Metal Complex Having General Formula (2) or its Tautomer as Partial Structure >>
A metal complex having the general formula (2) or a tautomer thereof according to the present invention as a partial structure (hereinafter also referred to as a metal complex represented by the general formula (2)) will be described.

In the general formula (2), R _e , R _f , R ₂₁ and R ₂₂ represent a hydrogen atom or a substituent. The substituent represented by R _e , R _f , R ₂₁ , R ₂₂ has the same meaning as the substituent represented by R _b in the general formula (1).

X ₂₁ represents a carbon atom or a nitrogen atom. X ₂₂ , X ₂₃ and X _{24 each} represent CR _g , a nitrogen atom or NR _h . R _g and R _h represent a hydrogen atom or a substituent. The substituent represented by R _g and R _h has the same meaning as the substituent represented by R _b in the general formula (1).

  nb and nc represent 1 or 2. n1 and n2 represent 0 or 1.

Ar ₁ and Ar ₂ each represents an aromatic carbocyclic group or an aromatic heterocyclic group. The aromatic carbocyclic group or aromatic heterocyclic group represented by Ar ₁ or Ar ₂ has the same meaning as the aromatic carbocyclic group or aromatic heterocyclic group represented by Ar ₀₀ in the general formula (1). .

X _b and X _c represent an oxygen atom, a sulfur atom or a nitrogen atom. M ₂₁ represents a group 8-10 metal in the periodic table. M ₂₁ is preferably iridium or platinum.

Bond between X ₂₁ and N, bond between N and X ₂₄ , bond between X ₂₄ and X ₂₃ , bond between X ₂₃ and X ₂₂ , between X ₂₂ and X ₂₁ Each of the bonds represents a single bond or a double bond.

<< Metal Complex Having General Formula (3) or its Tautomer as Partial Structure >>
A metal complex having the general formula (3) or a tautomer thereof according to the present invention as a partial structure (hereinafter, also referred to as a metal complex represented by the general formula (3)) will be described.

In the general formula (3), R ₃₁ , R ₃₂ , R ₃₃ and R ₃₄ represent a hydrogen atom or a substituent, but at least one represents an electron-withdrawing group. The substituent represented by R ₃₁ , R ₃₂ , R ₃₃ , and R ₃₄ has the same meaning as the substituent represented by R _b in the general formula (1).

The electron-withdrawing group represented by R ₃₁ , R ₃₂ , R ₃₃ , and R ₃₄ is a group having a Hammett's substituent constant σp exceeding 0. The electron-withdrawing group exemplified in the general formula (1) It is synonymous with. The present invention is not limited to these examples.

_X35 represents a carbon atom or a nitrogen atom.

X ₃₆ , X ₃₇ and X _{38 each} represent CR ₃₅ , a nitrogen atom or NR ₃₆ , at least one of which is CR ₃₅ . R ₃₅ and R ₃₆ represent a hydrogen atom or a substituent. At least one of R ₃₅ represents an aromatic carbocyclic group or an aromatic heterocyclic group. The substituents represented by R ₃₅ and R ₃₆ have the same meaning as the substituent represented by R _b in the general formula (1). The aromatic carbocyclic group or aromatic heterocyclic group represented by R ₃₅ has the same meaning as the aromatic carbocyclic group or aromatic heterocyclic group represented by Ar ₀₀ in formula (1).

M ₃₁ represents a group 8-10 metal in the periodic table. M ₃₁ is preferably iridium or platinum.

The bond between X ₃₅ and N, the bond between N and X ₃₈ , the bond between X ₃₈ and X ₃₇ , the bond between X ₃₇ and X _36, and the bond between X ₃₆ and X ₃₅ are each a single bond or a double bond. Represents a bond.

<< Metal Complex Having General Formula (4) or its Tautomer as Partial Structure >>
A metal complex having the general formula (4) or a tautomer thereof according to the present invention as a partial structure (hereinafter also referred to as a metal complex represented by the general formula (4)) will be described.

In the general formula (4), R ₄₁ , R ₄₂ , R ₄₃ and R ₄₄ represent a hydrogen atom or a substituent, and at least one of R ₄₁ and R ₄₂ represents an electron-withdrawing group. The substituent represented by R ₄₁ , R ₄₂ , R ₄₃ , R ₄₄ has the same definition as the substituent represented by R _b in the general formula (1). The electron withdrawing group represented by R ₄₁ , R ₄₂ , R ₄₃ and R ₄₄ has the same meaning as the electron withdrawing group represented by R ₃₁ , R ₃₂ , R ₃₃ and R ₃₄ in the general formula (3). is there.

X ₄₅ represents a carbon atom or a nitrogen atom.

X ₄₆ , X ₄₇ and X ₄₈ represent CR ₄₅ , a nitrogen atom or NR ₄₆ , at least one of which is CR ₄₅ . R ₄₅ and R ₄₆ represent a hydrogen atom or a substituent. At least one of R ₄₅ represents an aromatic carbocyclic group or an aromatic heterocyclic group. The substituent represented by R ₄₅ and R ₄₆ has the same meaning as the substituent represented by R _b in the general formula (1). The aromatic carbocyclic group or aromatic heterocyclic group represented by R ₄₅ has the same meaning as the aromatic carbocyclic group or aromatic heterocyclic group represented by Ar ₀₀ in formula (1).

M ₄₁ represents a group 8-10 metal in the periodic table. M ₄₁ is preferably iridium or platinum. The bond between X ₄₅ and N, the bond between N and X ₄₈ , the bond between X ₄₈ and X ₄₇ , the bond between X ₄₇ and X _46, and the bond between X ₄₆ and X ₄₅ are each a single bond or a double bond. Represents a bond.

  Hereinafter, specific examples of the metal complex having the general formula (1), (1A), (2) to (4) or a tautomer thereof as a partial structure according to the present invention will be shown. It is not limited.

These metal complexes are described in, for example, Organic Letter, vol. 16, p 2579-2581 (2001), Inorganic Chemistry, Vol. 30, No. 8, pp. 1685-1687 (1991), J. MoI. Am. Chem. Soc. , 123, 4304 (2001), Inorganic Chemistry, Vol. 40, No. 7, pages 1704-1711 (2001), Inorganic
Chemistry, Vol. 41, No. 12, 3055-3066 (2002), New Journal of Chemistry. , 26, 1171 (2002), Angelwande Chemie International Edition, 38, 1698-1712 (1999), Bulletin.
of the Chemical Society of Japan, Vol. 71, pp. 467-473 (1998), J. MoI. Am. Chem. Soc. 125, 18, 5274-5275 (2003), J. Am. Am. Chem. Soc. 125, No. 35, 10580-10585 (2003), and further by applying methods such as references described in these documents.

<< Application of organic EL element material containing metal complex to organic EL element >>
When producing the organic EL element of the present invention using the organic EL element material of the present invention, the organic EL element of the present invention is formed on the light emitting layer or the electron blocking layer in the constituent layers (details will be described later) of the organic EL element. It is preferable to use a material. In the light emitting layer, as described above, it is preferably used as a light emitting dopant.

(Light emitting host and light emitting dopant)
The mixing ratio of the light-emitting dopant to the light-emitting host, which is the host compound as the main component in the light-emitting layer, is preferably adjusted to a range of 0.1% by mass to less than 30% by mass.

  However, the light-emitting dopant may be a mixture of a plurality of types of compounds, and the partner to be mixed may be another metal complex having a different structure, or a phosphorescent dopant or a fluorescent dopant having another structure.

  Here, the dopant (phosphorescent dopant, fluorescent dopant, etc.) that may be used in combination with the metal complex used as the light emitting dopant will be described.

  The light-emitting dopant is roughly classified into two types: a fluorescent dopant that emits fluorescence and a phosphorescent dopant that emits phosphorescence.

  Representative examples of the former (fluorescent dopant) include coumarin dyes, pyran dyes, cyanine dyes, croconium dyes, squalium dyes, oxobenzanthracene dyes, fluorescein dyes, rhodamine dyes, pyrylium dyes, Examples include perylene dyes, stilbene dyes, polythiophene dyes, and rare earth complex phosphors.

  Typical examples of the latter (phosphorescent dopant) are preferably complex compounds containing metals of Group 8, Group 9, and Group 10 in the periodic table of elements, and more preferably iridium compounds and osmium compounds. Of these, iridium compounds are most preferred.

  Specifically, it is a compound described in the following patent publications.

  WO 00/70655 pamphlet, JP 2002-280178, JP 2001-181616, JP 2002-280179, JP 2001-181617, JP 2002-280180, JP 2001-247859, JP 2002-299060, JP 2001-313178, JP 2002-302671, JP 2001-345183, JP 2002-324679, International Publication No. 02/15645 pamphlet, JP 2002-332291 A, JP 2002-50484 A, JP 2002-332292 A, JP 2002-83684 A, JP 2002-540572 A, JP 2002-2002 A. No. 117978, JP 20 JP-A-2-338588, JP-A-2002-170684, JP-A-2002-352960, WO01 / 93642, JP-A-2002-50483, JP-A-2002-1000047, JP-A-2002. No. -173744, JP-A No. 2002-359082, JP-A No. 2002-17584, JP-A No. 2002-363552, JP-A No. 2002-184582, JP-A No. 2003-7469, JP-T-2002-525808. Gazette, JP2003-7471, JP2002-525833, JP2003-31366, JP2002-226495, JP2002-234894, JP2002-2335076 JP 2002-241751 A JP 2001-319779, JP 2001-319780, JP 2002-62824, JP 2002-1000047, JP 2002-203679, JP 2002-343572, JP 2002-203678 gazette etc.

  Some examples are shown below.

(Light emitting host)
A light-emitting host (also simply referred to as a host) means a compound having the largest mixing ratio (mass) in a light-emitting layer composed of two or more kinds of compounds. Simply referred to as a dopant). " For example, if the light emitting layer is composed of two types of compound A and compound B and the mixing ratio is A: B = 10: 90, compound A is a dopant compound and compound B is a host compound. Furthermore, if a light emitting layer is comprised from 3 types of compound A, compound B, and compound C, and the mixing ratio is A: B: C = 5: 10: 85, compound A and compound B are dopant compounds, Compound C is a host compound.

  As the luminescent host used in the present invention, a compound having a wavelength shorter than the phosphorescence 0-0 band of the luminescent dopant used in combination is preferable, and the phosphorescent 0-0 band is 480 nm or less as the luminescent dopant. In the case of using a compound containing the above light emitting component, the phosphorescent 0-0 band is preferably 450 nm or less as the light emitting host.

  The light-emitting host used in the present invention is not particularly limited in terms of structure, but is typically a carbazole derivative, a triarylamine derivative, an aromatic borane derivative, a nitrogen-containing heterocyclic compound, a thiophene derivative, a furan derivative, an oligo Examples thereof include those having a basic skeleton such as an arylene compound, or derivatives having a ring structure in which at least one carbon atom of a hydrocarbon ring constituting a carboline derivative or a carboline ring of the carboline derivative is substituted with a nitrogen atom. .

  Of these, carbazole derivatives, carboline derivatives, and derivatives having a ring structure in which at least one carbon atom of the hydrocarbon ring constituting the carboline ring of the carboline derivative is substituted with a nitrogen atom are preferably used.

  Specific examples are given below, but the present invention is not limited thereto.

  The light emitting host of the present invention may be a low molecular compound, a high molecular compound having a repeating unit, or a low molecular compound having a polymerizable group such as a vinyl group or an epoxy group (evaporation polymerizable light emitting host).

  As the light-emitting host, a compound having a hole transporting ability and an electron transporting ability, preventing emission light from being increased in wavelength, and having a high Tg (glass transition temperature) is preferable.

  As specific examples of the light-emitting host, compounds described in the following documents are suitable. For example, Japanese Patent Laid-Open Nos. 2001-257076, 2002-308855, 2001-313179, 2002-319491, 2001-357777, 2002-334786, JP2002-8860, JP2002-334787, JP2002-15871, JP2002-334788, JP2002-43056, JP2002-334789, JP JP 2002-75645 A, JP 2002-338579 A, JP 2002-105445 A, JP 2002-343568 A, JP 2002-141173 A, JP 2002-352957 A, JP 2002-2002 A. No. 203683, JP-A-2002-3632 7, JP 2002-231453, JP 2003-3165, JP 2002-234888, JP 2003-27048, JP 2002-255934, JP 2002-286061. JP, JP-A-2002-280183, JP-A-2002-299060, JP-A-2002-302516, JP-A-2002-305083, JP-A-2002-305084, JP-A-2002-308837, etc. .

  Next, a configuration of a typical organic EL element will be described.

<< Constituent layers of organic EL elements >>
The constituent layers of the organic EL element of the present invention will be described.

Although the preferable specific example of the layer structure of the organic EL element of this invention is shown below, this invention is not limited to these.
(I) Anode / hole transport layer / light emitting layer / hole blocking layer / electron transport layer / cathode (ii) Anode / electron blocking layer / light emitting layer / hole blocking layer / electron transport layer / cathode (iii) anode / Hole transport layer / electron blocking layer / light emitting layer / hole blocking layer / electron transport layer / cathode (iv) anode / hole transport layer / electron blocking layer / light emitting layer / hole blocking layer / electron transport layer / cathode ( v) Anode / hole transport layer / electron blocking layer / light emitting layer / hole blocking layer / electron transport layer / cathode buffer layer / cathode (vi) anode / anode buffer layer / hole transport layer / electron blocking layer / light emitting layer / Hole blocking layer / electron transport layer / cathode buffer layer / cathode (vii) anode / anode buffer layer / hole transport layer / electron blocking layer / light emitting layer / hole blocking layer / electron transport layer / cathode buffer layer / cathode 《Blocking layer (electron blocking layer, hole blocking layer)》
The blocking layer (for example, electron blocking layer, hole blocking layer) according to the present invention will be described.

  In the present invention, the organic EL device material of the present invention is preferably used for the hole blocking layer, the electron blocking layer, and the like, and particularly preferably used for the electron blocking layer.

  When the organic EL device material of the present invention is contained in a hole blocking layer and an electron blocking layer, the metal complex according to any one of claims 1 to 6 is blocked by holes. It may be contained in a state of 100% by mass as a layer constituent component such as a layer or an electron blocking layer, or may be mixed with other organic compounds.

  The thickness of the blocking layer according to the present invention is preferably 3 to 100 nm, and more preferably 5 to 30 nm.

《Hole blocking layer》
The hole blocking layer has the function of an electron transport layer in a broad sense, and is made of a material that has a function of transporting electrons but has a very small ability to transport holes, and blocks holes while transporting electrons. Thus, the probability of recombination of electrons and holes can be improved.

  Examples of the hole blocking layer include those disclosed in JP-A-11-204258, JP-A-11-204359, and “Organic EL device and its forefront of industrialization (issued by NTS, Inc. on November 30, 1998)”. The hole blocking (hole block) layer described in page 237 and the like can be applied as the hole blocking layer according to the present invention. Moreover, the structure of the electron carrying layer mentioned later can be used as a hole-blocking layer concerning this invention as needed.

  The organic EL device of the present invention has a hole blocking layer as a constituent layer, and the hole blocking layer has at least one carbon atom of the hydrocarbon ring constituting the carboline derivative or the carboline ring of the carboline derivative. It is preferable to contain a derivative having a ring structure substituted with a nitrogen atom.

《Electron blocking layer》
On the other hand, the electron blocking layer has a function of a hole transport layer in a broad sense, and is made of a material that has a function of transporting holes and has an extremely small ability to transport electrons, and transports electrons while transporting holes. By blocking, the recombination probability of electrons and holes can be improved. Moreover, the structure of the positive hole transport layer mentioned later can be used as an electron blocking layer as needed.

  In the present invention, the organic EL device material of the present invention is preferably used for the adjacent layer adjacent to the light emitting layer, that is, the hole blocking layer and the electron blocking layer, and particularly used for the electron blocking layer. preferable.

《Hole transport layer》
The hole transport layer includes a material having a function of transporting holes, and in a broad sense, a hole injection layer and an electron blocking layer are also included in the hole transport layer. The hole transport layer can be provided as a single layer or a plurality of layers.

  The hole transport material is not particularly limited, and is conventionally used as a hole charge injection / transport material in an optical transmission material or a well-known material used for a hole injection layer or a hole transport layer of an EL element. Any one can be selected and used.

  The hole transport material has one of hole injection or transport and electron barrier properties, and may be either organic or inorganic. For example, triazole derivatives, oxadiazole derivatives, imidazole derivatives, polyarylalkane derivatives, pyrazoline derivatives and pyrazolone derivatives, phenylenediamine derivatives, arylamine derivatives, amino-substituted chalcone derivatives, oxazole derivatives, styrylanthracene derivatives, fluorenone derivatives, hydrazone derivatives, stilbenes Derivatives, silazane derivatives, aniline copolymers, conductive polymer oligomers, particularly thiophene oligomers, and the like can be given.

  As the hole transport material, those described above can be used, and it is preferable to use a porphyrin compound, an aromatic tertiary amine compound, and a styrylamine compound, particularly an aromatic tertiary amine compound.

  Representative examples of aromatic tertiary amine compounds and styrylamine compounds include N, N, N ′, N′-tetraphenyl-4,4′-diaminophenyl; N, N′-diphenyl-N, N′— Bis (3-methylphenyl)-[1,1′-biphenyl] -4,4′-diamine (TPD); 2,2-bis (4-di-p-tolylaminophenyl) propane; 1,1-bis (4-di-p-tolylaminophenyl) cyclohexane; N, N, N ′, N′-tetra-p-tolyl-4,4′-diaminobiphenyl; 1,1-bis (4-di-p-tolyl) Aminophenyl) -4-phenylcyclohexane; bis (4-dimethylamino-2-methylphenyl) phenylmethane; bis (4-di-p-tolylaminophenyl) phenylmethane; N, N'-diphenyl-N, N ' − (4-methoxyphenyl) -4,4'-diaminobiphenyl; N, N, N ', N'-tetraphenyl-4,4'-diaminodiphenyl ether; 4,4'-bis (diphenylamino) quadriphenyl; N, N, N-tri (p-tolyl) amine; 4- (di-p-tolylamino) -4 '-[4- (di-p-tolylamino) styryl] stilbene; 4-N, N-diphenylamino- (2-diphenylvinyl) benzene; 3-methoxy-4′-N, N-diphenylaminostilbenzene; N-phenylcarbazole, and two more described in US Pat. No. 5,061,569 Having a condensed aromatic ring of, for example, 4,4'-bis [N- (1-naphthyl) -N-phenylamino] biphenyl (NPD), JP-A-4-308 4,4 ', 4 "-tris [N- (3-methylphenyl) -N-phenylamino] triphenylamine in which three triphenylamine units described in Japanese Patent No. 88 are linked in a starburst type ( MTDATA) and the like.

  Furthermore, a polymer material in which these materials are introduced into a polymer chain or these materials are used as a polymer main chain can also be used.

  In addition, inorganic compounds such as p-type-Si and p-type-SiC can also be used as the hole injection material and the hole transport material.

  The hole transport layer can be formed by thinning the hole transport material by a known method such as a vacuum deposition method, a spin coating method, a casting method, an ink jet method, or an LB method. Although there is no restriction | limiting in particular about the film thickness of a positive hole transport layer, Usually, it is about 5 nm-5000 nm. The hole transport layer may have a single layer structure composed of one or more of the above materials.

《Electron transport layer》
The electron transport layer is made of a material having a function of transporting electrons, and in a broad sense, an electron injection layer and a hole blocking layer are also included in the electron transport layer. The electron transport layer can be provided with a single layer or multiple layers.

  Conventionally, in the case of a single-layer electron transport layer and a plurality of layers, the following materials are used as the electron transport material (also serving as a hole blocking material) used for the electron transport layer adjacent to the cathode side with respect to the light emitting layer. Are known.

  Further, the electron transport layer only needs to have a function of transmitting electrons injected from the cathode to the light emitting layer, and any material can be selected from conventionally known compounds. .

  Examples of materials used for this electron transport layer (hereinafter referred to as electron transport materials) include heterocyclic tetracarboxylic acid anhydrides such as nitro-substituted fluorene derivatives, diphenylquinone derivatives, thiopyran dioxide derivatives, naphthalene perylene, carbodiimides, At least one of the carbon atoms of the fluorenylidenemethane derivative, anthraquinodimethane and anthrone derivative, oxadiazole derivative, carboline derivative, or the hydrocarbon ring constituting the carboline ring of the carboline derivative is substituted with a nitrogen atom Examples thereof include derivatives having a ring structure. Furthermore, in the oxadiazole derivative, a thiadiazole derivative in which the oxygen atom of the oxadiazole ring is substituted with a sulfur atom, and a quinoxaline derivative having a quinoxaline ring known as an electron-withdrawing group can also be used as an electron transport material. .

  Furthermore, a polymer material in which these materials are introduced into a polymer chain or these materials are used as a polymer main chain can also be used.

  In addition, metal complexes of 8-quinolinol derivatives such as tris (8-quinolinol) aluminum (Alq), tris (5,7-dichloro-8-quinolinol) aluminum, tris (5,7-dibromo-8-quinolinol) aluminum, Tris (2-methyl-8-quinolinol) aluminum, tris (5-methyl-8-quinolinol) aluminum, bis (8-quinolinol) zinc (Znq), etc., and the central metals of these metal complexes are In, Mg, Cu , Ca, Sn, Ga, or Pb can also be used as an electron transport material. In addition, metal-free or metal phthalocyanine, or those having terminal ends substituted with an alkyl group or a sulfonic acid group can be preferably used as the electron transporting material. In addition, the distyrylpyrazine derivative exemplified as the material of the light emitting layer can also be used as an electron transport material, and similarly to the hole injection layer and the hole transport layer, inorganic such as n-type-Si and n-type-SiC can be used. A semiconductor can also be used as an electron transport material.

  The electron transport layer can be formed by thinning the electron transport material by a known method such as a vacuum deposition method, a spin coating method, a casting method, an ink jet method, or an LB method. Although there is no restriction | limiting in particular about the film thickness of an electron carrying layer, Usually, it is about 5-5000 nm. The electron transport layer may have a single layer structure composed of one or more of the above materials.

  Next, an injection layer used as a constituent layer of the organic EL element of the present invention will be described.

<< Injection layer >>: Electron injection layer, hole injection layer The injection layer is provided as necessary, and there are an electron injection layer and a hole injection layer, and as described above, between the anode and the light emitting layer or the hole transport layer, and You may exist between a cathode, a light emitting layer, or an electron carrying layer.

  An injection layer is a layer provided between an electrode and an organic layer in order to lower drive voltage or improve light emission luminance. “Organic EL element and its forefront of industrialization (issued on November 30, 1998 by NTS Corporation) 2), Chapter 2, “Electrode Materials” (pages 123 to 166) in detail, and includes a hole injection layer (anode buffer layer) and an electron injection layer (cathode buffer layer).

  The details of the anode buffer layer (hole injection layer) are described in JP-A-9-45479, JP-A-9-260062, JP-A-8-288069 and the like. As a specific example, copper phthalocyanine is used. Examples thereof include a phthalocyanine buffer layer represented by an oxide, an oxide buffer layer represented by vanadium oxide, an amorphous carbon buffer layer, and a polymer buffer layer using a conductive polymer such as polyaniline (emeraldine) or polythiophene.

  The details of the cathode buffer layer (electron injection layer) are described in JP-A-6-325871, JP-A-9-17574, JP-A-10-74586, and the like. Specifically, strontium or aluminum Metal buffer layer represented by lithium fluoride, alkali metal compound buffer layer represented by lithium fluoride, alkaline earth metal compound buffer layer represented by magnesium fluoride, oxide buffer layer represented by aluminum oxide, etc. It is done.

  The buffer layer (injection layer) is preferably a very thin film, and the film thickness is preferably in the range of 0.1 to 100 nm, although it depends on the material.

  This injection layer can be formed by thinning the above material by a known method such as a vacuum deposition method, a spin coating method, a casting method, an ink jet method, or an LB method. Although there is no restriction | limiting in particular about the film thickness of an injection | pouring layer, Usually, it is about 5-5000 nm. This injection layer may have a single layer structure composed of one or more of the above materials.

"anode"
As the anode according to the organic EL device of the present invention, an electrode having a work function (4 eV or more) metal, alloy, electrically conductive compound and a mixture thereof as an electrode material is preferably used. Specific examples of such electrode materials include metals such as Au, and conductive transparent materials such as CuI, indium tin oxide (ITO), SnO ₂ and ZnO. Alternatively, an amorphous material such as IDIXO (In ₂ O ₃ —ZnO) capable of forming a transparent conductive film may be used. For the anode, a thin film may be formed by depositing these electrode materials by a method such as vapor deposition or sputtering, and a pattern having a desired shape may be formed by a photolithography method, or when the pattern accuracy is not required (100 μm or more) Degree), a pattern may be formed through a mask having a desired shape when the electrode material is deposited or sputtered. When light emission is extracted from the anode, it is desirable that the transmittance is greater than 10%, and the sheet resistance as the anode is preferably several hundred Ω / □ or less. Further, although the film thickness depends on the material, it is usually selected in the range of 10 to 1000 nm, preferably 10 to 200 nm.

"cathode"
On the other hand, as the cathode according to the present invention, a cathode having a work function (4 eV or less) metal (referred to as an electron injecting metal), an alloy, an electrically conductive compound, and a mixture thereof is used. Specific examples of such electrode materials include sodium, sodium-potassium alloy, magnesium, lithium, magnesium / copper mixture, magnesium / silver mixture, magnesium / aluminum mixture, magnesium / indium mixture, aluminum / aluminum oxide (Al ₂ O ₃ ) Mixtures, indium, lithium / aluminum mixtures, rare earth metals and the like. Among these, a mixture of an electron injecting metal and a second metal which is a stable metal having a larger work function value than this, such as a magnesium / silver mixture, magnesium, from the viewpoint of electron injectability and durability against oxidation, etc. / Aluminum mixtures, magnesium / indium mixtures, aluminum / aluminum oxide (Al ₂ O ₃ ) mixtures, lithium / aluminum mixtures, aluminum and the like are preferred. The cathode can be produced by forming a thin film of these electrode materials by a method such as vapor deposition or sputtering. The sheet resistance as the cathode is preferably several hundred Ω / □ or less, and the film thickness is usually selected in the range of 10 to 1000 nm, preferably 50 to 200 nm. In order to transmit light, if either one of the anode or the cathode of the organic EL element is transparent or translucent, the light emission luminance is improved, which is convenient.

<< Substrate (also referred to as substrate, substrate, support, etc.) >>
The substrate of the organic EL device of the present invention is not particularly limited to the type of glass, plastic, etc., and is not particularly limited as long as it is transparent. Examples of substrates that are preferably used include glass, quartz, A light transmissive resin film can be mentioned. A particularly preferable substrate is a resin film that can give flexibility to the organic EL element.

  Examples of the resin film include polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polyethersulfone (PES), polyetherimide, polyetheretherketone, polyphenylene sulfide, polyarylate, polyimide, polycarbonate (PC), and cellulose triacetate. Examples thereof include films made of (TAC), cellulose acetate propionate (CAP) and the like.

An inorganic or organic film or a hybrid film of both may be formed on the surface of the resin film, and the film should be a high barrier film having a water vapor transmission rate of 0.01 g / m ² · day · atm or less. preferable.

  The external extraction efficiency at room temperature of light emission of the organic El device of the present invention is preferably 1% or more, more preferably 2% or more. Here, the external extraction quantum efficiency (%) = the number of photons emitted to the outside of the organic EL element / the number of electrons sent to the organic EL element × 100.

  Further, a hue improving filter such as a color filter may be used in combination.

  When used in lighting applications, a film (such as an antiglare film) that has been roughened to reduce unevenness in light emission can be used in combination.

  When used as a multicolor display device, it is composed of organic EL elements having at least two different light emission maximum wavelengths. A suitable example for producing an organic EL element will be described.

<< Method for producing organic EL element >>
As an example of the method for producing the organic EL device of the present invention, a method for producing an organic EL device comprising an anode / hole injection layer / hole transport layer / light emitting layer / hole blocking layer / electron transport layer / cathode buffer layer / cathode. Will be described.

  First, a thin film made of a desired electrode material, for example, an anode material is formed on a suitable substrate by a method such as vapor deposition or sputtering so as to have a film thickness of 1 μm or less, preferably 10 to 200 nm, thereby producing an anode. To do. Next, a thin film containing an organic compound such as a hole injection layer, a hole transport layer, a light emitting layer, a hole blocking layer, or an electron transport layer, which is an element material, is formed thereon.

As a method for thinning a thin film containing an organic compound, there are a spin coat method, a cast method, an ink jet method, a vapor deposition method, a printing method, etc., but a uniform film is easily obtained and pinholes are not easily generated. In view of the above, the vacuum evaporation method or the spin coating method is particularly preferable. Further, different film forming methods may be applied for each layer. When employing a vapor deposition method for film formation, the vapor deposition conditions vary depending on the type of compound used, but generally a boat heating temperature of 50 to 450 ° C., a vacuum degree of 10 ⁻⁶ to 10 ⁻² Pa, and a vapor deposition rate of 0.01 It is desirable to select appropriately within a range of ˜50 nm / second, a substrate temperature of −50 to 300 ° C., and a film thickness of 0.1 to 5 μm.

  After these layers are formed, a thin film made of a cathode material is formed thereon by a method such as vapor deposition or sputtering so as to have a thickness of 1 μm or less, preferably in the range of 50 to 200 nm, and a cathode is provided. Thus, a desired organic EL element can be obtained. The organic EL element is preferably produced from the hole injection layer to the cathode consistently by a single evacuation, but may be taken out halfway and subjected to different film forming methods. At that time, it is necessary to consider that the work is performed in a dry inert gas atmosphere.

<Display device>
The display device of the present invention will be described. The display device of the present invention has the organic EL element.

  The display device of the present invention may be single color or multicolor, but here, the multicolor display device will be described. In the case of a multicolor display device, a shadow mask is provided only at the time of forming a light emitting layer, and a film can be formed on one surface by a vapor deposition method, a casting method, a spin coating method, an ink jet method, a printing method, or the like.

  When patterning is performed only on the light-emitting layer, the method is not limited, but a vapor deposition method, an inkjet method, and a printing method are preferable. In the case of using a vapor deposition method, patterning using a shadow mask is preferable.

  Moreover, it is also possible to reverse the production order to produce the cathode, the electron transport layer, the hole blocking layer, the light emitting layer, the hole transport layer, and the anode in this order.

  When a DC voltage is applied to the multicolor display device thus obtained, light emission can be observed by applying a voltage of about 2 to 40 V with the positive polarity of the anode and the negative polarity of the cathode. Further, even when a voltage is applied with the opposite polarity, no current flows and no light emission occurs. Further, when an AC voltage is applied, light is emitted only when the anode is in the + state and the cathode is in the-state. The alternating current waveform to be applied may be arbitrary.

  The multicolor display device can be used as a display device, a display, and various light emission sources. In a display device or display, full-color display is possible by using three types of organic EL elements of blue, red, and green light emission.

  Examples of the display device and the display include a television, a personal computer, a mobile device, an AV device, a character broadcast display, and an information display in a car. In particular, it may be used as a display device for reproducing still images and moving images, and the driving method when used as a display device for reproducing moving images may be either a simple matrix (passive matrix) method or an active matrix method.

  Light emitting sources include household lighting, interior lighting, clock and liquid crystal backlights, billboard advertisements, traffic lights, light sources for optical storage media, light sources for electrophotographic copying machines, light sources for optical communication processors, light sources for optical sensors, etc. For example, but not limited to.

《Lighting device》
The lighting device of the present invention will be described. The illuminating device of this invention has the said organic EL element.

  The organic EL element of the present invention may be used as an organic EL element having a resonator structure. The use of the organic EL element having such a resonator structure is as a light source for an optical storage medium, an electrophotographic copying machine, and the like. Light sources, optical communication processor light sources, optical sensor light sources, and the like. Moreover, you may use for the said use by making a laser oscillation.

  Further, the organic EL element of the present invention may be used as a kind of lamp for illumination or exposure light source, a projection device for projecting an image, or a type for directly viewing a still image or a moving image. It may be used as a display device (display). When used as a display device for reproducing moving images, the driving method may be either a simple matrix (passive matrix) method or an active matrix method. Alternatively, a full-color display device can be manufactured by using two or more organic EL elements of the present invention having different emission colors.

  Hereinafter, an example of a display device having the organic EL element of the present invention will be described with reference to the drawings.

  FIG. 1 is a schematic diagram illustrating an example of a display device including organic EL elements. It is a schematic diagram of a display such as a mobile phone that displays image information by light emission of an organic EL element.

  The display 1 includes a display unit A having a plurality of pixels, a control unit B that performs image scanning of the display unit A based on image information, and the like.

  The control unit B is electrically connected to the display unit A, and sends a scanning signal and an image data signal to each of the plurality of pixels based on image information from the outside. The pixels for each scanning line are converted into image data signals by the scanning signal. In response to this, light is sequentially emitted and image scanning is performed to display image information on the display unit A.

  FIG. 2 is a schematic diagram of the display unit A.

  The display unit A includes a wiring unit including a plurality of scanning lines 5 and data lines 6, a plurality of pixels 3 and the like on a substrate. The main members of the display unit A will be described below.

  In the figure, the light emitted from the pixel 3 is extracted in the direction of the white arrow (downward).

  The scanning lines 5 and the plurality of data lines 6 in the wiring portion are each made of a conductive material, and the scanning lines 5 and the data lines 6 are orthogonal to each other in a lattice shape and are connected to the pixels 3 at the orthogonal positions (details are shown in FIG. Not shown).

  When a scanning signal is applied from the scanning line 5, the pixel 3 receives an image data signal from the data line 6 and emits light according to the received image data. Full color display is possible by appropriately arranging pixels in the red region, the green region, and the blue region that emit light on the same substrate.

  Next, the light emission process of the pixel will be described.

  FIG. 3 is a schematic diagram of a pixel.

  The pixel includes an organic EL element 10, a switching transistor 11, a driving transistor 12, a capacitor 13, and the like. A full color display can be performed by using red, green, and blue light emitting organic EL elements as the organic EL elements 10 in a plurality of pixels, and juxtaposing them on the same substrate.

  In FIG. 3, an image data signal is applied from the control unit B to the drain of the switching transistor 11 through the data line 6. When a scanning signal is applied from the control unit B to the gate of the switching transistor 11 via the scanning line 5, the driving of the switching transistor 11 is turned on, and the image data signal applied to the drain is supplied to the capacitor 13 and the driving transistor 12. Is transmitted to the gate.

  By transmitting the image data signal, the capacitor 13 is charged according to the potential of the image data signal, and the drive of the drive transistor 12 is turned on. The drive transistor 12 has a drain connected to the power supply line 7 and a source connected to the electrode of the organic EL element 10, and the power supply line 7 connects to the organic EL element 10 according to the potential of the image data signal applied to the gate. Current is supplied.

  When the scanning signal is moved to the next scanning line 5 by the sequential scanning of the control unit B, the driving of the switching transistor 11 is turned off. However, even if the driving of the switching transistor 11 is turned off, the capacitor 13 maintains the potential of the charged image data signal, so that the driving of the driving transistor 12 is kept on and the next scanning signal is applied. Until then, the light emission of the organic EL element 10 continues. When the scanning signal is next applied by sequential scanning, the driving transistor 12 is driven according to the potential of the next image data signal synchronized with the scanning signal, and the organic EL element 10 emits light.

  That is, the organic EL element 10 emits light by the switching transistor 11 and the drive transistor 12 that are active elements for the organic EL element 10 of each of the plurality of pixels, and the light emission of the organic EL element 10 of each of the plurality of pixels 3. It is carried out. Such a light emitting method is called an active matrix method.

  Here, the light emission of the organic EL element 10 may be light emission of a plurality of gradations by a multi-value image data signal having a plurality of gradation potentials, or on / off of a predetermined light emission amount by a binary image data signal. But you can.

  The potential of the capacitor 13 may be held continuously until the next scanning signal is applied, or may be discharged immediately before the next scanning signal is applied.

  In the present invention, not only the active matrix method described above, but also a passive matrix light emission drive in which the organic EL element emits light according to the data signal only when the scanning signal is scanned.

  FIG. 4 is a schematic view of a passive matrix display device. In FIG. 4, a plurality of scanning lines 5 and a plurality of image data lines 6 are provided in a lattice shape so as to face each other with the pixel 3 interposed therebetween.

  When the scanning signal of the scanning line 5 is applied by sequential scanning, the pixels 3 connected to the applied scanning line 5 emit light according to the image data signal.

  In the passive matrix system, the pixel 3 has no active element, and the manufacturing cost can be reduced.

  The organic EL material of the present invention can also be applied to an organic EL element that emits substantially white light as a lighting device. A plurality of light emitting colors are simultaneously emitted by a plurality of light emitting materials to obtain white light emission by color mixing. The combination of a plurality of emission colors may include three emission maximum wavelengths of the three primary colors of blue, green, and blue, or two using the relationship of complementary colors such as blue and yellow, blue green and orange, etc. The thing containing the light emission maximum wavelength may be used.

  In addition, a combination of light emitting materials for obtaining a plurality of emission colors is a combination of a plurality of phosphorescent or fluorescent materials that emit light, and a light emitting material that emits fluorescence or phosphorescence, and light from the light emitting material. Any combination with a dye material that emits light as excitation light may be used, but in the white organic EL device according to the present invention, a plurality of light-emitting dopants need only be mixed and mixed. A mask is provided only at the time of forming a light emitting layer, a hole transport layer, an electron transport layer, etc., and it is only necessary to simply arrange them separately by coating with the mask. Since other layers are common, patterning of the mask or the like is unnecessary. In addition, for example, an electrode film can be formed by a vapor deposition method, a cast method, a spin coating method, an ink jet method, a printing method, etc., and productivity is also improved. According to this method, unlike a white organic EL device in which light emitting elements of a plurality of colors are arranged in parallel in an array, the elements themselves are luminescent white.

  The light emitting material used for the light emitting layer is not particularly limited. For example, in the case of a backlight in a liquid crystal display element, the metal complex according to the present invention is also known so as to be adapted to the wavelength range corresponding to the CF (color filter) characteristics. Any one of the light emitting materials may be selected and combined to be whitened.

  Thus, in addition to the display device and display, the white light-emitting organic EL element of the present invention can be used as various light-emitting light sources, lighting devices, household lighting, interior lighting, and a kind of lamp such as an exposure light source. It is also useful for display devices such as backlights for liquid crystal display devices.

  In addition, backlights such as clocks, signboard advertisements, traffic lights, light sources such as optical storage media, light sources for electrophotographic copying machines, light sources for optical communication processing machines, light sources for optical sensors, etc. There are a wide range of uses such as household appliances.

  EXAMPLES Hereinafter, although an Example demonstrates this invention, this invention is not limited to these. Moreover, the compound used for an Example is shown below.

Example 1
<< Production of Organic EL Element 1-1 >>
After patterning on a substrate (made by NH Techno Glass Co., Ltd .: NA-45) having a 150 nm ITO film formed on glass as an anode, the transparent support substrate provided with this ITO transparent electrode was ultrasonically cleaned with iso-propyl alcohol. Then, it was dried with dry nitrogen gas, and UV ozone cleaning was performed for 5 minutes. The transparent support substrate is fixed to a substrate holder of a commercially available vacuum deposition apparatus, while α-NPD, CBP, Ir-12, BCP, and Alq ₃ are placed in five tantalum resistance heating boats, respectively. (First vacuum chamber).

  Further, lithium fluoride was placed in a tantalum resistance heating boat, and aluminum was placed in a tungsten resistance heating boat, which were attached to a second vacuum tank of a vacuum evaporation apparatus.

First, after reducing the pressure of the first vacuum tank to 4 × 10 ⁻⁴ Pa, the heating boat containing α-NPD was energized and heated, and the transparent support substrate was deposited at a deposition rate of 0.1 to 0.2 nm / sec. A hole injection / transport layer was provided by vapor deposition to a thickness of 30 nm.

  Further, the heating boat containing CBP and the boat containing Ir-12 are energized independently to adjust the deposition rate of CBP as a light emitting host and Ir-12 as a light emitting dopant to 100: 3. A light emitting layer was provided by vapor deposition so as to have a thickness of 30 nm.

Subsequently, the heating boat containing BCP was energized and heated to provide a hole blocking layer having a thickness of 10 nm at a deposition rate of 0.1 to 0.2 nm / second. Further, the heating boat containing Alq ₃ was heated by energization to provide an electron transport layer having a film thickness of 40 nm at a deposition rate of 0.1 to 0.2 nm / second.

  Next, after the element deposited up to the electron transport layer was transferred to the second vacuum chamber while being vacuumed, it was remotely controlled from the outside of the apparatus so that a stainless steel rectangular perforated mask was placed on the electron transport layer. Installed.

After depressurizing the second vacuum tank to 2 × 10 ⁻⁴ Pa, a cathode buffer layer having a film thickness of 0.5 nm was provided at a deposition rate of 0.01 to 0.02 nm / second by energizing a boat containing lithium fluoride. Next, a boat containing aluminum was energized, and a cathode having a film thickness of 150 nm was attached at a deposition rate of 1 to 2 nm / second. Further, this element was transferred to a glove box under nitrogen atmosphere (a glove box substituted with high-purity nitrogen gas with a purity of 99.999% or more) without being exposed to the atmosphere, and the interior as shown in FIG. 5 was substituted with nitrogen. An organic EL element 1-1 was produced with a sealing structure.

  In addition, barium oxide 105 which is a water catching agent is a glass sealed can 104 made of high-purity barium oxide powder manufactured by Aldrich with a fluororesin semi-permeable membrane (Microtex S-NTF8031Q made by Nitto Denko) with an adhesive. The material pasted on was prepared and used in advance. An ultraviolet curable adhesive 107 was used for bonding the sealing can and the organic EL element, and both were bonded to each other by irradiation with an ultraviolet lamp to produce a sealing element.

  In FIG. 5, 101 is a glass substrate provided with a transparent electrode, 102 is an organic EL layer composed of the hole injection / transport layer, light emitting layer, hole blocking layer, electron transport layer, and the like, and 103 is a cathode.

<< Production of Organic EL Elements 1-2 to 1-24 >>
In the production of the organic EL element 1-1, the organic EL elements 1-2 to 1-24 were produced in the same manner except that the light emitting host and the light emitting dopant were changed as shown in Table 1.

<< Evaluation of organic EL elements >>
The obtained organic EL elements 1-1 to 1-24 were evaluated as follows.

(External quantum efficiency)
By lighting the organic EL element under a constant current condition of room temperature (about 23 to 25 ° C.) and ^2.5 mA / cm ² , and measuring the emission luminance (L) [cd / m ² ] immediately after the start of lighting, The external extraction quantum efficiency (η) was calculated. Here, CS-1000 (manufactured by Minolta) was used for measurement of light emission luminance. The external extraction quantum efficiency was expressed as a relative value with the organic EL element 1-1 as 100.

(Luminescent life)
At room temperature the organic EL device, the continuous lighting by constant current condition of 2.5 mA / cm ^2, to measure the time taken to become half of the initial luminance (τ _1/2). The light emission lifetime was expressed as a relative value at which the organic EL element 1-1 was set to 100.

  The obtained results are shown in Table 1.

  From Table 1, the organic EL device produced using the metal complex represented by the general formula (1), (1A) or general formula (2) according to the present invention has higher light emission than the organic EL device of the comparative example. It is clear that an increase in efficiency and lifetime can be achieved.

  Further, the effect of the present invention can be further improved by using a carboline derivative or a derivative having a ring structure in which at least one carbon atom of the hydrocarbon ring constituting the carboline ring of the carboline derivative is further substituted with a nitrogen atom in the light emitting layer. Improvement was seen.

Example 2
<< Preparation of Organic EL Element 2-1 >>
After patterning on a substrate (made by NH Techno Glass Co., Ltd .: NA-45) having a 150 nm ITO film formed on glass as an anode, the transparent support substrate provided with this ITO transparent electrode was ultrasonically cleaned with iso-propyl alcohol. Then, it was dried with dry nitrogen gas, and UV ozone cleaning was performed for 5 minutes.

The transparent support substrate is fixed to a substrate holder of a commercially available vacuum deposition apparatus, while α-NPD, CBP, Ir-13, BCP, and Alq ₃ are placed in five tantalum resistance heating boats, respectively. (First vacuum chamber).

  Further, lithium fluoride was placed in a tantalum resistance heating boat, and aluminum was placed in a tungsten resistance heating boat, which were attached to a second vacuum tank of a vacuum evaporation apparatus.

First, after reducing the pressure of the first vacuum tank to 4 × 10 ⁻⁴ Pa, the heating boat containing α-NPD was energized and heated, and the transparent support substrate was deposited at a deposition rate of 0.1 to 0.2 nm / sec. A hole injection / transport layer was provided by vapor deposition to a thickness of 30 nm.

  Further, the heating boat containing CBP and the boat containing Ir-13 are energized independently to adjust the deposition rate of CBP as the light emitting host and Ir-13 as the light emitting dopant to 100: 6. A light emitting layer was provided by vapor deposition so as to have a thickness of 30 nm.

Subsequently, the heating boat containing BCP was energized and heated to provide a hole blocking layer having a thickness of 10 nm at a deposition rate of 0.1 to 0.2 nm / second. Further, the heating boat containing Alq ₃ was heated by energization to provide an electron transport layer having a film thickness of 40 nm at a deposition rate of 0.1 to 0.2 nm / second.

  Next, after the element deposited up to the electron transport layer was transferred to the second vacuum chamber while being vacuumed, it was remotely controlled from the outside of the apparatus so that a stainless steel rectangular perforated mask was placed on the electron transport layer. Installed.

After depressurizing the second vacuum tank to 2 × 10 ⁻⁴ Pa, a cathode buffer layer having a film thickness of 0.5 nm was provided at a deposition rate of 0.01 to 0.02 nm / second by energizing a boat containing lithium fluoride. Next, a boat containing aluminum was energized, and a cathode having a film thickness of 150 nm was attached at a deposition rate of 1 to 2 nm / second. Further, this element was transferred to a glove box under nitrogen atmosphere (a glove box substituted with high-purity nitrogen gas with a purity of 99.999% or more) without being exposed to the atmosphere, and the interior as shown in FIG. 5 was substituted with nitrogen. An organic EL element 2-1 was produced with a sealing structure. In addition, barium oxide 105 which is a water trapping agent is a glass-sealed can 104 made of high-purity barium oxide powder manufactured by Aldrich with a fluororesin-based semipermeable membrane (Microtex S-NTF8031Q made by Nitto Denko) with an adhesive. The material pasted on was prepared and used in advance. An ultraviolet curable adhesive 107 was used for bonding the sealing can and the organic EL element, and both were bonded to each other by irradiation with an ultraviolet lamp to produce a sealing element. In FIG. 5, 101 is a glass substrate provided with a transparent electrode, 102 is an organic EL layer composed of the hole injection / transport layer, light emitting layer, hole blocking layer, electron transport layer, and the like, and 103 is a cathode.

<< Production of Organic EL Elements 2-2 to 2-16 >>
In the production of the organic EL element 2-1, organic EL elements 2-2 to 2-16 were produced in the same manner except that the light emitting host and the light emitting dopant were changed as shown in Table 2.

<< Evaluation of organic EL elements >>
About the obtained organic EL elements 2-1 to 2-16, the external extraction quantum efficiency was evaluated in the same manner as in Example 1. The external extraction quantum efficiency was expressed as a relative value with the organic EL element 2-1 being 100. Moreover, the light emission lifetime was measured by the following method.

(Luminescent life)
At room temperature the organic EL element 2-1~2-16, 2.5mA / cm ² of make continuous lighting by constant current conditions, the time required to become 90% of the initial luminance (τ _1/9) Was measured. In addition, the light emission lifetime was represented by the relative value which sets the organic EL element 2-1 to 100.

  The obtained results are shown in Table 2.

  From Table 2, the organic EL element produced using the metal complex represented by the general formula (1A), (3) or general formula (4) according to the present invention is higher than the organic EL element of the comparative example. It is clear that the light emission efficiency and the light emission life can be extended.

  Furthermore, by using a carboline derivative or a derivative having a ring structure in which at least one carbon atom of a hydrocarbon ring constituting the carboline ring of the carboline derivative is further substituted with a nitrogen atom, in combination with the light emitting layer, The improvement of the effect was seen.

Example 3
<< Production of Organic EL Element 3-1 >>
After patterning on a substrate (made by NH Techno Glass Co., Ltd .: NA-45) having a 150 nm ITO film formed on glass as an anode, the transparent support substrate provided with this ITO transparent electrode was ultrasonically cleaned with iso-propyl alcohol. Then, it was dried with dry nitrogen gas, and UV ozone cleaning was performed for 5 minutes.

The transparent support substrate is fixed to a substrate holder of a commercially available vacuum deposition apparatus, while m-MTDATXA, H1, Ir-12, BCP, and Alq ₃ are placed in five tantalum resistance heating boats, respectively. (First vacuum chamber).

  Further, lithium fluoride was placed in a tantalum resistance heating boat, and aluminum was placed in a tungsten resistance heating boat, which were attached to a second vacuum tank of a vacuum evaporation apparatus.

First, after reducing the pressure of the first vacuum tank to 4 × 10 ⁻⁴ Pa, the heating boat containing m-MTDATXA was energized and heated, and the transparent support substrate was deposited at a deposition rate of 0.1 to 0.2 nm / sec. The film was deposited to a thickness of 40 nm to provide a hole injection / transport layer.

  Further, the heating boat containing H1 and the boat containing Ir-12 are energized independently to adjust the deposition rate of H1 as a light emitting host and Ir-12 as a light emitting dopant to 100: 6. A light emitting layer was provided by vapor deposition so as to have a thickness of 30 nm.

Subsequently, the heating boat containing BCP was energized and heated to provide a hole blocking layer having a thickness of 10 nm at a deposition rate of 0.1 to 0.2 nm / second. Further, the heating boat containing Alq ₃ was energized and heated to provide an electron transport layer having a film thickness of 20 nm at a deposition rate of 0.1 to 0.2 nm / second.

  Next, after the element deposited up to the electron transport layer was transferred to the second vacuum chamber while being vacuumed, it was remotely controlled from the outside of the apparatus so that a stainless steel rectangular perforated mask was placed on the electron transport layer. Installed.

After depressurizing the second vacuum tank to 2 × 10 ⁻⁴ Pa, a cathode buffer layer having a film thickness of 0.5 nm was provided at a deposition rate of 0.01 to 0.02 nm / second by energizing a boat containing lithium fluoride. Next, a boat containing aluminum was energized, and a cathode having a film thickness of 150 nm was attached at a deposition rate of 1 to 2 nm / second. Further, this element was transferred to a glove box under nitrogen atmosphere (a glove box substituted with high-purity nitrogen gas with a purity of 99.999% or more) without being exposed to the atmosphere, and the interior as shown in FIG. 5 was substituted with nitrogen. An organic EL element 3-1 was produced with a sealing structure. In addition, barium oxide 105 which is a water trapping agent is a glass-sealed can 104 made of high-purity barium oxide powder manufactured by Aldrich with a fluororesin-based semipermeable membrane (Microtex S-NTF8031Q made by Nitto Denko) with an adhesive. The material pasted on was prepared and used in advance. An ultraviolet curable adhesive 107 was used for bonding the sealing can and the organic EL element, and both were bonded to each other by irradiation with an ultraviolet lamp to produce a sealing element. In FIG. 5, 101 is a glass substrate provided with a transparent electrode, 102 is an organic EL layer composed of the hole injection / transport layer, light emitting layer, hole blocking layer, electron transport layer, and the like, and 103 is a cathode.

<< Production of Organic EL Elements 3-2 to 3-19 >>
In the production of the organic EL element 3-1, organic EL elements 3-2 to 3-19 were produced in the same manner except that the light emitting host and the light emitting dopant were changed as shown in Table 3.

<< Evaluation of organic EL elements >>
The obtained organic EL devices 3-1 to 3-19 were evaluated for external extraction quantum efficiency and light emission lifetime by the same method as in Example 1. The external extraction quantum efficiency and the light emission lifetime are expressed as relative values with the organic EL element 3-1 as 100. Moreover, the chromaticity difference was measured by the following method.

(Chromaticity difference)
The organic EL element is lighted at room temperature (about 23 ° C. to 25 ° C.) under a constant current condition of ^2.5 mA / cm ² , and the CIE chromaticity ((x, y) = (a , B)) were measured, and the difference between NTSC (modern) and blue ((x, y) = (0.155, 0.07)) was calculated as Δ.

  Here, (DELTA) was calculated | required according to the following formula | equation, and the measurement of CIE chromaticity used CS-1000 (made by Minolta).

Δ = (| 0.155-a | 2 + | 0.07-b | 2) 1/2
The obtained results are shown in Table 3.

  From Table 3, it is clear that the organic EL device produced using the metal complex according to the present invention can achieve higher luminous efficiency and longer lifetime than the organic EL device of the comparative example.

  Further, by using in combination with the hole blocking layer, a carboline derivative or a derivative having a ring structure in which at least one carbon atom of the hydrocarbon ring constituting the carboline ring of the carboline derivative is further substituted with a nitrogen atom. Improvement of the effect of the invention was observed.

Example 4
<< Preparation of Organic EL Element 4-1 >>
After patterning on a substrate (made by NH Techno Glass Co., Ltd .: NA-45) having a 150 nm ITO film formed on glass as an anode, the transparent support substrate provided with this ITO transparent electrode was ultrasonically cleaned with iso-propyl alcohol. Then, it was dried with dry nitrogen gas, and UV ozone cleaning was performed for 5 minutes. This transparent support substrate is fixed to a substrate holder of a commercially available vacuum deposition apparatus, while α-NPD, Comparison 2, CBP, Ir-1, BCP, and Alq ₃ are placed in a tantalum resistance heating boat, respectively, and vacuum deposition is performed. It was attached to an apparatus (first vacuum chamber).

  Further, lithium fluoride was placed in a tantalum resistance heating boat, and aluminum was placed in a tungsten resistance heating boat, which were attached to a second vacuum tank of a vacuum evaporation apparatus.

First, after reducing the pressure of the first vacuum tank to 4 × 10 ⁻⁴ Pa, the heating boat containing α-NPD was energized and heated, and the transparent support substrate was deposited at a deposition rate of 0.1 to 0.2 nm / sec. The film was deposited to a thickness of 40 nm to provide a hole injection / transport layer.

Next, after reducing the pressure of the first vacuum tank to 4 × 10 ⁻⁴ Pa, the heating boat containing the comparison 2 was energized and heated, and the transparent support substrate was deposited at a deposition rate of 0.1 to 0.2 nm / sec. The film was deposited to a thickness of 20 nm, and an electron blocking (blocking) layer was provided.

  Further, the heating boat containing CBP and the boat containing Ir-1 are energized independently to adjust the deposition rate of CBP as a light emitting host and Ir-1 as a light emitting dopant to 100: 7. A light emitting layer was provided by vapor deposition so as to have a thickness of 30 nm.

Then, the heating boat containing BCP was energized and heated, and a hole blocking layer having a thickness of 15 nm was provided at a deposition rate of 0.1 to 0.2 nm / second. Further, the heating boat containing Alq ₃ was energized and heated to provide an electron transport layer having a film thickness of 20 nm at a deposition rate of 0.1 to 0.2 nm / second.

  Next, after the element deposited up to the electron transport layer was transferred to the second vacuum chamber while being vacuumed, it was remotely controlled from the outside of the apparatus so that a stainless steel rectangular perforated mask was placed on the electron transport layer. Installed.

After depressurizing the second vacuum tank to 2 × 10 ⁻⁴ Pa, a cathode buffer layer having a film thickness of 0.5 nm was provided at a deposition rate of 0.01 to 0.02 nm / second by energizing a boat containing lithium fluoride. Next, a boat containing aluminum was energized, and a cathode having a film thickness of 150 nm was attached at a deposition rate of 1 to 2 nm / second. Further, this element was transferred to a glove box under nitrogen atmosphere (a glove box substituted with high-purity nitrogen gas with a purity of 99.999% or more) without being exposed to the atmosphere, and the interior as shown in FIG. 5 was substituted with nitrogen. An organic EL element 4-1 was produced with a sealing structure.

  In addition, barium oxide 105 which is a water catching agent is a glass sealed can 104 made of high-purity barium oxide powder manufactured by Aldrich with a fluororesin semi-permeable membrane (Microtex S-NTF8031Q made by Nitto Denko) with an adhesive. The material pasted on was prepared and used in advance. An ultraviolet curable adhesive 107 was used for bonding the sealing can and the organic EL element, and both were bonded to each other by irradiation with an ultraviolet lamp to produce a sealing element.

  In FIG. 5, 101 is a glass substrate provided with a transparent electrode, 102 is an organic EL layer comprising the hole injection / transport layer, electron blocking layer, light emitting layer, hole blocking layer, electron transport layer, etc. 103 is a cathode. .

<< Production of Organic EL Elements 4-2 to 4-9 >>
In the production of the organic EL element 1-1, organic EL elements 4-2 to 4-9 were produced in the same manner except that the electron blocking material was changed as shown in Table 4.

<< Evaluation of organic EL elements >>
The obtained organic EL elements 4-1 to 4-9 were evaluated for external extraction quantum efficiency and light emission lifetime in the same manner as in Example 1. The external extraction quantum efficiency and the light emission lifetime are expressed as relative values with the organic EL element 4-1 as 100.

  Table 4 shows the obtained results.

  From Table 4, it is clear that the organic EL device produced using the metal complex according to the present invention can achieve higher luminous efficiency and longer lifetime than the organic EL device of the comparative example.

Example 5
An anode of indium tin oxide (ITO, indium / tin = 95/5 molar ratio) was formed on a glass support substrate of 25 mm × 25 mm × 0.5 mm by a sputtering method using a direct current power (thickness: 200 nm). The surface resistance of this anode was 10Ω / □. Polyvinylcarbazole (hole transporting binder polymer) / Ir-13 (blue light-emitting orthometalated complex) / 2- (4-biphenylyl) -5- (4-t-butylphenyl) -1, A dichloroethane solution in which 3,4-oxadiazole (electron transport material) = 200/2/50 mass ratio was dissolved was applied by a spin coater to obtain a light emitting layer having a thickness of 100 nm. A patterned mask (a mask with a light emission area of 5 mm × 5 mm) is placed on the organic compound layer, and lithium fluoride 0.5 nm is deposited as a cathode buffer layer and aluminum 150 nm is deposited as a cathode in a deposition apparatus to form a cathode. Provided. A light emitting element was manufactured by extending aluminum lead wires from the anode and the cathode, respectively. The element is put in a glove box substituted with nitrogen gas, and sealed with a glass sealing container using an ultraviolet curable adhesive (manufactured by Chiba Nagase, XNR 5493) to give a blue light emitting organic EL element 5-1. Produced.

<< Production of organic EL elements 5-2 to 5-5 >>
In the production of the organic EL element 5-1, organic EL elements 5-2 to 5-5 were produced in the same manner except that the luminescent dopant was changed as shown in Table 5.

<< Evaluation of organic EL elements >>
About the obtained organic EL elements 5-1 to 5-5, the light emission luminance and the light emission efficiency were measured as follows.

(Luminance, luminous efficiency)
Using Toyo Technica source measure unit type 2400, a direct current voltage is applied to the organic EL element to emit light, and a light emission luminance (Cd / m ² ) and ^2.5 mA / cm ² when a direct current voltage of 10 V is applied. Luminous efficiency (lm / W) when passing current was measured.

  The results obtained are shown in Table 5.

  From Table 5, it is clear that the organic EL element produced using the metal complex according to the present invention can achieve high luminous efficiency and high luminance as compared with the organic EL element of the comparative example.

Example 6
<Production of full-color display device>
(Production of blue light emitting element)
The organic EL element 1-5 of Example 1 was used as a blue light emitting element.

(Production of green light emitting element)
The organic EL element 4-7 of Example 4 was used as a green light emitting element.

(Production of red light emitting element)
In the organic EL element 2-1 of Example 2, a red light emitting element was produced in the same manner except that Ir-13 was changed to Ir-9, and this was used as a red light emitting element.

  The red, green, and blue light-emitting organic EL elements produced above were juxtaposed on the same substrate to produce an active matrix type full-color display device having a configuration as shown in FIG. In FIG. 2, only the schematic diagram of the display part A of the produced display device is shown. That is, a wiring portion including a plurality of scanning lines 5 and data lines 6 on the same substrate, and a plurality of juxtaposed pixels 3 (light emission color is a red region pixel, a green region pixel, a blue region pixel, etc.) The scanning lines 5 and the plurality of data lines 6 in the wiring portion are each made of a conductive material, and the scanning lines 5 and the data lines 6 are orthogonal to each other in a lattice shape and are connected to the pixels 3 at the orthogonal positions ( Details are not shown). The plurality of pixels 3 are driven by an active matrix system provided with an organic EL element corresponding to each emission color, a switching transistor as an active element, and a driving transistor, and a scanning signal is applied from a scanning line 5. Then, an image data signal is received from the data line 6 and light is emitted according to the received image data. In this way, a full color display device was produced by appropriately juxtaposing red, green, and blue pixels.

  It has been found that when this full-color display device is driven, high brightness, high durability, and a clear full-color moving image display can be obtained.

Example 7
<< Preparation of white light emitting element and white lighting device >>
The electrode of the transparent electrode substrate of Example 1 was patterned to 20 mm × 20 mm, and α-NPD was formed as a hole injection / transport layer with a thickness of 25 nm thereon as in Example 1, and further CBP The heating boat containing the above, the boat containing the compound 1-11 according to the present invention and the boat containing Ir-9 are energized independently, respectively, CBP as the light emitting host and the compound according to the present invention as the light emitting dopant Evaporation rates of 1-11 and Ir-9 were adjusted to be 100: 5: 0.6, and vapor deposition was performed to a thickness of 30 nm to provide a light emitting layer.

Next, BCP was deposited to a thickness of 10 nm to provide a hole blocking layer. Furthermore, Alq ₃ was deposited at 40 nm to provide an electron transport layer.

  Next, as in Example 1, a square perforated mask having the same shape as the transparent electrode made of stainless steel was placed on the electron injection layer, lithium fluoride 0.5 nm as the cathode buffer layer and aluminum 150 nm as the cathode. Was deposited.

  This element was provided with a sealing can having the same method and the same structure as in Example 1 to produce a flat lamp. FIG. 6 shows a schematic diagram of a flat lamp. FIG. 6A shows a schematic plan view, and FIG. 6B shows a schematic cross-sectional view.

  When this flat lamp was energized, almost white light was obtained, and it was found that it could be used as a lighting device.

Claims (13)

An organic electroluminescent device material, which is a metal complex having the following general formula (1) or a tautomer thereof as a partial structure.

(In the formula, R ₁₁ , R ₁₂ , R ₁₃ , R ₁₄ , R ₁₅ each represents a hydrogen atom or a substituent, X ₀₁ , X ₀₂ , X ₀₃ , X ₀₄ each represents a carbon atom or a nitrogen atom; ₀₁ represents a group 8-10 metal in the periodic table, a bond between X ₀₁ and N, a bond between N and X _04, a bond between X ₀₄ and X ₀₃ , a bond between X ₀₃ and X ₀₂ , X ₀₂ And X ₀₁ each represents an end bond or a double bond, and u2 represents an integer of 0 to 3, provided that at least two of R _{11 to} R ₁₄ are aromatic groups, or R ₁₁ to At least one of R ₁₄ is an electron-withdrawing group and R ₁₅ is an aromatic group, or at least two of R _{11 to} R _{14 are-} (Ar ₀ ) _u0- (X) _a0- ( R ₀₎ is a group represented by _u1. here, Ar ₀ is Represents an aromatic group, X represents an oxygen atom, a sulfur atom or a nitrogen atom, R ₀ represents a substituent, u0 and a0 are both 0 or 1, u1 represents 1 or 2. However, u0 and a0 is not 0 at all.) The organic electroluminescent device material according to claim 1, which is a metal complex having the following general formula (1A) or a tautomer thereof as a partial structure.

(In the formula, R _b represents a hydrogen atom or a substituent. X ₁₁ represents a carbon atom or a nitrogen atom. X ₁₂ , X ₁₃ and X ₁₄ represent CR _c , a nitrogen atom or NR _d . R _c , R _d represents a hydrogen atom or a substituent, ma and mb represent an integer satisfying 2 ≦ ma ≦ 4 and ma + mb = 4, Ar ₀₀ represents an aromatic carbocyclic group or an aromatic heterocyclic group, and M ₁₁ represents an element. Represents a group 8-10 metal in the periodic table, a bond between X ₁₁ and N, a bond between N and X ₁₄ , a bond between X ₁₄ and X ₁₃ , a bond between X ₁₃ and X ₁₂ , X ₁₂ and X The bond to ₁₁ represents a single bond or a double bond, respectively.) The organic electroluminescence device material according to claim 1, which is a metal complex having the following general formula (2) or a tautomer thereof as a partial structure.

(In the formula, R _e , R _f , R ₂₁ and R ₂₂ represent a hydrogen atom or a substituent. X ₂₁ represents a carbon atom or a nitrogen atom. X ₂₂ , X ₂₃ and X ₂₄ represent CR _g , a nitrogen atom or NR _h represents R _g and R _h each represents a hydrogen atom or a substituent, nb and nc represent 1 or 2, n1 and n2 represent 0 or ₁ , Ar ₁ and Ar ₂ represent aromatic carbocyclic groups Or an aromatic heterocyclic group, X _b and X _{c each} represents an oxygen atom, a sulfur atom or a nitrogen atom, and M ₂₁ represents a group 8-10 metal in the periodic table of the elements between X ₂₁ and N A bond, a bond between N and X ₂₄ , a bond between X ₂₄ and X ₂₃ , a bond between X ₂₃ and X ₂₂ and a bond between X ₂₂ and X ₂₁ are each a single bond or Represents a double bond.) 2. The organic electroluminescent element material according to claim 1, which is a metal complex having the following general formula (3) or a tautomer thereof as a partial structure.

(In the formula, R ₃₁ , R ₃₂ , R ₃₃ and R ₃₄ represent a hydrogen atom or a substituent, but at least one represents an electron-withdrawing group. X ₃₅ represents a carbon atom or a nitrogen atom. X ₃₆ , X ₃₇ and X ₃₈ represent CR ₃₅ , a nitrogen atom or NR ₃₆ , at least one of which is CR _35. R ₃₅ and R ₃₆ each represents a hydrogen atom or a substituent, and at least one of R ₃₅ is aromatic. M ₃₁ represents a group 8-10 metal in the periodic table, a bond between X ₃₅ and N, a bond between N and X ₃₈ , X ₃₈ and X ₃₇ And the bond between X ₃₇ and X ₃₆ and the bond between X ₃₆ and X ₃₅ each represent a single bond or a double bond.) The organic electroluminescent device material according to claim 1, which is a metal complex having the following general formula (4) or a tautomer thereof as a partial structure.

(In the formula, R ₄₁ , R ₄₂ , R ₄₃ and R ₄₄ represent a hydrogen atom or a substituent, but at least one of R ₄₁ and R ₄₂ represents an electron-withdrawing group. X ₄₅ represents a carbon atom or a nitrogen atom. _{.X 46,} X 47 representing _{a, X 48} is _{CR 45, .R 45} represents a nitrogen atom or _{NR 46,} representing the at least one of which is a _{CR 45 .R 45, R 46} is a hydrogen atom or a substituent At least one of them represents an aromatic carbocyclic group or an aromatic heterocyclic group, M ₄₁ represents a group 8-10 metal in the periodic table, a bond between X ₄₅ and N, a bond between N and X ₄₈ , X ₄₈ and X ₄₇ , X ₄₇ and X _46, and X ₄₆ and X ₄₅ each represent a single bond or a double bond.) 2. The organic electroluminescent element material according to claim ₁ , wherein M01 is iridium or platinum. An organic electroluminescent element comprising the organic electroluminescent element material according to claim 1. An organic electroluminescence element having a light emitting layer as a constituent layer, wherein the light emitting layer contains the organic electroluminescence element material according to claim 1. An organic electroluminescence device having an electron blocking layer as a constituent layer, wherein the electron blocking layer contains the organic electroluminescence device material according to claim 1. An organic electroluminescence device having a light emitting layer as a constituent layer, wherein the light emitting layer is a ring in which at least one of carbon atoms of a carboline derivative or a hydrocarbon ring constituting a carboline ring of the carboline derivative is substituted with a nitrogen atom. The organic electroluminescence device according to claim 7, further comprising a derivative having a structure. An organic electroluminescence device having a hole blocking layer as a constituent layer, wherein the hole blocking layer is substituted with a nitrogen atom at least one of carbon atoms of a carboline derivative or a hydrocarbon ring constituting a carboline ring of the carboline derivative. The organic electroluminescence device according to claim 7, further comprising a derivative having a ring structure. A display device comprising the organic electroluminescence element according to claim 7. An illuminating device comprising the organic electroluminescence element according to claim 7.