JPWO2016181772A1 - π-conjugated compound, organic electroluminescence element material, luminescent thin film, organic electroluminescence element, display device and illumination device - Google Patents

Abstract

（一般式（１）中、Ｄ^１及びＤ²は、それぞれ独立に、電子供与性基で置換されたアリール基、置換されていてもよい電子供与性の複素環基、及び置換されていてもよいアミノ基からなる群より選ばれる電子供与性基Ｄを表し、Ｍ^１〜Ｍ^４は、それぞれ独立して、窒素原子又は−Ｃ−Ｚを表し、Ｍ^１〜Ｍ^４のうちの少なくとも一つは窒素原子であり、Ｍ^１〜Ｍ^４のいずれかが−Ｃ−Ｚの場合、Ｚはそれぞれ独立して水素原子、重水素原子、又は置換基を表す。）The present invention provides a π-conjugated compound that can increase the light emission efficiency without increasing the light emission wavelength. The π-conjugated compound of the present invention is a compound having a structure represented by the following general formula (1).
[Chemical 1]

(In General Formula (1), D ¹ and D ² are each independently an aryl group substituted with an electron donating group, an optionally substituted electron donating heterocyclic group, or a substituted aryl group. Represents an electron donating group D selected from the group consisting of a good amino group, M ^{1 to} M ⁴ each independently represent a nitrogen atom or —C—Z, and at least one of M ^{1 to} M ⁴ ; Is a nitrogen atom, and when any of M ^{1 to} M ⁴ is —C—Z, each Z independently represents a hydrogen atom, a deuterium atom, or a substituent.

Description

  The present invention relates to a π-conjugated compound, an organic electroluminescence element material, a light-emitting thin film, an organic electroluminescence element, and a display device and an illumination apparatus provided with the organic electroluminescence element. More specifically, the present invention relates to a π-conjugated compound having improved luminous efficiency.

  An organic electroluminescence element (also referred to as “organic electroluminescence element” or “organic EL element”) using organic electroluminescence (Electro Luminescence: hereinafter abbreviated as “EL”) enables planar light emission. This technology has already been put into practical use as a new light emitting system. Organic EL elements are not only applied to electronic displays but also recently applied to lighting equipment, and their development is expected.

There are two types of emission methods for organic EL elements: phosphorescence emission, which emits light when returning from the triplet excited state to the ground state, and fluorescence emission, which emits light when returning from the singlet excited state to the ground state. There is a street.
When an electric field is applied to the organic EL element, holes and electrons are injected from the anode and the cathode, respectively, and recombine in the light emitting layer to generate excitons. At this time, since singlet excitons and triplet excitons are generated at a ratio of 25%: 75%, phosphorescence using triplet excitons is theoretically higher in internal quantum than fluorescence. It is known that efficiency can be obtained.
However, in order to actually obtain high quantum efficiency in the phosphorescence emission method, it is necessary to use a complex using a rare metal such as iridium or platinum as a central metal. There is concern that price will be a major industrial issue.

On the other hand, various developments have been made to improve the light emission efficiency in the fluorescent light emitting type, and a new movement has recently been made.
For example, in Patent Document 1, a phenomenon in which singlet excitons are generated by collision of two triplet excitons (triplet-triplet annihilation: hereinafter, abbreviated as “TTA” as appropriate. Triplet-Triplet Fusion: “TTF”) In particular, a technology for increasing the efficiency of a fluorescent element by efficiently causing TTA is disclosed. Although this technology improves the luminous efficiency of fluorescent materials by up to 2-3 times that of conventional fluorescent materials, the theoretical singlet exciton generation efficiency in TTA is only about 40%, so phosphorescence is still emitted. Compared to the above, there is a problem of high luminous efficiency.

  Furthermore, in recent years, a phenomenon (thermally activated delayed fluorescence (""), where a reverse intersystem crossing from a triplet exciton to a singlet exciton (hereinafter referred to as "RISC" as appropriate) occurs. It is also referred to as “thermally excited delayed fluorescence”: Thermally Activated Delayed Fluorescence (hereinafter abbreviated as “TADF” as appropriate), and the possibility of use in organic EL devices has been reported (for example, (See Patent Document 2, Non-Patent Document 1, and Non-Patent Document 2.) By using delayed fluorescence by this TADF mechanism, 100% internal quantum is theoretically equivalent to phosphorescence emission even in fluorescence emission by electric field excitation. Efficiency becomes possible.

In order to develop the TADF phenomenon, it is necessary that reverse intersystem crossing from triplet excitons generated by electric field excitation to singlet excitons at room temperature or light emitting layer temperature in the light emitting element occurs. Furthermore, a singlet exciton generated by crossing between inverses emits fluorescence similarly to a 25% singlet exciton generated by direct excitation, so that an internal quantum efficiency of 100% is theoretically possible. To this Gyakuko intersystem crossing occurs, the absolute value of the difference between the lowest excited singlet energy level (S ₁₎ and the lowest triplet excitation energy level (T ₁₎ (hereinafter referred to as Delta] E _ST.) Is very Small is essential.

  Furthermore, it is known that when a light emitting layer composed of a host compound and a light emitting compound contains a compound exhibiting TADF properties as a third component (assist dopant) in the light emitting layer, it is effective for high light emission efficiency (non-lighting). (See Patent Document 3). By generating 25% singlet excitons and 75% triplet excitons on the assist dopant by electric field excitation, the triplet excitons generate singlet excitons with reverse intersystem crossing (RISC). be able to. The energy of singlet excitons can be transferred to the luminescent compound by fluorescence resonance energy transfer (hereinafter abbreviated as “FRET” where appropriate), and light can be emitted by the energy transferred from the luminescent compound. It becomes. Therefore, theoretically, it becomes possible to cause the luminescent compound to emit light using 100% exciton energy, and high luminous efficiency is exhibited.

To minimize Delta] E _ST in an organic compound, be localized without mixing highest occupied molecular orbital of the molecule (HOMO) and the lowest unoccupied molecular orbital (LUMO) it is desirable.

1 and 2 are schematic diagrams showing energy diagrams of a compound that expresses a TADF phenomenon (TADF compound) and a general fluorescent compound. For example, in 2CzPN having the structure shown in FIG. 1, HOMO is localized at the 1st and 2nd carbazolyl groups on the benzene ring, and LUMO is localized at the 4th and 5th cyano groups. Therefore, it is possible to separate the HOMO and LUMO of 2CzPN, ΔE _ST express TADF phenomenon extremely small. On the other hand, in 2CzXy (FIG. 2) in which the cyano group at the 4-position and 5-position of 2CzPN is replaced with a methyl group, the structure is similar, but HOMO and LUMO seen in 2CzPN cannot be clearly separated, so ΔE _ST cannot be reduced, and the TADF phenomenon cannot be expressed.

  In the prior art, in order to clearly separate HOMO and LUMO, a technique using a strong electron-donating group or electron-withdrawing group is known. However, the use of a strong electron donating group or electron withdrawing group forms a strong intramolecular charge transfer (CT) excited state, causing the absorption spectrum and emission spectrum to become longer, and the emission wavelength. There is a problem that it is difficult to control. Conversely, if the electron donating property or the electron withdrawing property is weakened in order to control the emission wavelength, it will hinder the expression of the TADF phenomenon. Therefore, a new technique for causing the TADF phenomenon to occur while controlling the emission wavelength is desired.

International Publication No. 2010/134350 JP2013-116975A

H. Uoyama, et al. , Nature, 2012, 492, 234-238. Q. Zhang et al. , Nature, Photonics, 2014, 8, 326-332. H. Nakatanani, et al. , Nature Communication, 2014, 5, 4016-4022.

  The present invention has been made in view of the above problems and circumstances, and a problem to be solved is to provide a new π-conjugated compound that can increase the light emission efficiency without increasing the light emission wavelength. Another object of the present invention is to provide an organic electroluminescent element material containing the π-conjugated compound, a light-emitting thin film, and a display device and an illumination device provided with the organic electroluminescent element.

As a result of examining the cause of the above-mentioned problem in order to solve the above-mentioned problems, the present inventor contains a π-conjugated compound having an electron-donating part at the para position of the nitrogen-containing aromatic six-membered ring that is an electron-withdrawing part. The present inventors have conceived a new organic electroluminescence device characterized by the above, and found that the light emission efficiency can be improved, thereby reaching the present invention.
That is, the said subject which concerns on this invention is solved by the following means.

（一般式（１）中、
Ｄ^１及びＤ²は、それぞれ独立に、電子供与性基で置換されたアリール基、置換されていてもよい電子供与性の複素環基、及び置換されていてもよいアミノ基からなる群より選ばれる電子供与性基Ｄを表し、
Ｍ^１〜Ｍ^４は、それぞれ独立して、窒素原子又は−Ｃ−Ｚを表し、Ｍ^１〜Ｍ^４のうちの少なくとも一つは窒素原子であり、Ｍ^１〜Ｍ^４のいずれかが−Ｃ−Ｚの場合、Ｚはそれぞれ独立して水素原子、重水素原子、又は置換基を表す。）
［２］ 前記置換基は、前記電子供与性基Ｄ又はアルキル基であるか、又は
フッ素原子、シアノ基、フッ素原子で置換されたアルキル基、置換されていてもよいカルボニル基、置換されていてもよいスルホニル基、置換されていてもよいホスフィンオキサイド基、置換されていてもよいボリル基、電子吸引性基で置換されていてもよいアリール基、及び置換されていてもよい電子吸引性の複素環基からなる群より選ばれる電子吸引性基Ａである、［１］に記載のπ共役系化合物。
［３］ 下記一般式（２）〜（２１）のいずれかで表される、［１］又は［２］に記載のπ共役系化合物。

（一般式（２）〜（２１）中、
Ｄ^１〜Ｄ^６は、それぞれ独立して、前記電子供与性基Ｄを表し、
Ｚ^１〜Ｚ^４は、それぞれ独立して、水素原子、重水素原子、アルキル基又は前記電子吸引性基Ａを表す。）
［４］ 前記一般式（２）〜（２１）において、Ｚ^１〜Ｚ^４が電子吸引性基Ａである、［３］に記載のπ共役系化合物。
［５］ 前記π共役系化合物において、Ｄ^１＝Ｄ^２＝Ｄ^３＝Ｄ^４＝Ｄ^５＝Ｄ^６とＺ^１＝Ｚ^２＝Ｚ^３＝Ｚ^４のうち少なくとも一方を満たす、［３］又は［４］に記載のπ共役系化合物。
［６］ 前記π共役系化合物の最低励起一重項準位と最低励起三重項準位とのエネルギー差の絶対値（ΔＥ_ＳＴ）が０．５０ｅＶ以下である、［１］〜［５］のいずれかに記載のπ共役系化合物。In view of the above problems, the first of the present invention relates to a π-conjugated compound.
[1] A π-conjugated compound having a structure represented by the following general formula (1).

(In general formula (1),
D ¹ and D ² are each independently selected from the group consisting of an aryl group substituted with an electron donating group, an optionally substituted electron donating heterocyclic group, and an optionally substituted amino group. Represents an electron donating group D
M ¹ ~M ⁴ each independently represents a nitrogen atom or ^-C-Z, at least one of M 1 ~M ⁴ is a nitrogen ^atom, or is -C of M 1 ~M ⁴ In the case of -Z, Z represents a hydrogen atom, a deuterium atom, or a substituent each independently. )
[2] The substituent is the electron donating group D or an alkyl group, or a fluorine atom, a cyano group, an alkyl group substituted with a fluorine atom, an optionally substituted carbonyl group, A sulfonyl group that may be substituted, a phosphine oxide group that may be substituted, a boryl group that may be substituted, an aryl group that may be substituted with an electron-withdrawing group, and an electron-withdrawing complex that may be substituted The π-conjugated compound according to [1], which is an electron-withdrawing group A selected from the group consisting of a cyclic group.
[3] The π-conjugated compound according to [1] or [2], represented by any one of the following general formulas (2) to (21).

(In the general formulas (2) to (21),
D ^{1 to} D ⁶ each independently represent the electron donating group D;
Z ^{1 to} Z ⁴ each independently represent a hydrogen atom, a deuterium atom, an alkyl group or the electron-withdrawing group A. )
[4] The π-conjugated compound according to [3], wherein in the general formulas (2) to (21), Z ^{1 to} Z ⁴ are an electron-withdrawing group A.
[5] In the π-conjugated compound, at ^{least one} of D ¹ = D ² = D ³ = D ⁴ = D ⁵ = D ⁶ and Z ¹ = Z ² = Z ³ = Z ⁴ is satisfied, [3] or [Pi] Conjugated compound according to [4].
[6] Any of [1] to [5], wherein an absolute value (ΔE _ST ) of an energy difference between the lowest excited singlet level and the lowest excited triplet level of the π-conjugated compound is 0.50 eV or less. A π-conjugated compound according to claim 1.

The second aspect of the present invention relates to an organic electroluminescent element material and an organic electroluminescent element using the π-conjugated compound of the present invention.
[7] An organic electroluminescence device material comprising the π-conjugated compound according to any one of [1] to [6].
[8] A luminescent thin film containing the π-conjugated compound according to any one of [1] to [6].
[9] including an anode, a cathode, and a light emitting layer provided between the anode and the cathode,
An organic electroluminescence device, wherein at least one layer of the light emitting layer contains the π-conjugated compound according to any one of [1] to [6].
[10] The organic electroluminescent element according to [9], wherein the light emitting layer includes the π-conjugated compound and at least one of a fluorescent light emitting compound and a phosphorescent light emitting compound.
[11] The organic electroluminescent element according to [9], wherein the light emitting layer includes the π-conjugated compound, at least one of a fluorescent light emitting compound and a phosphorescent light emitting compound, and a host material.

The third aspect of the present invention relates to a display device and a lighting device using the organic electroluminescence element of the present invention.
[12] A display device comprising the organic electroluminescence element according to any one of [9] to [11].
[13] An illumination device having the organic electroluminescence element according to any one of [9] to [11].

  The above-described means of the present invention can provide a new π-conjugated compound that achieves improved luminous efficiency. In addition, the π-conjugated compound can provide an organic electroluminescent element material, a light-emitting thin film containing the organic electroluminescent element material, and a display device and a lighting device including the organic electroluminescent element.

  The expression mechanism or action mechanism of the effect of the present invention is presumed as follows.

  The present application has found that an organic electroluminescence device comprising a π-conjugated compound having an electron donating moiety at the para-position of a nitrogen-containing aromatic six-membered ring, which is an electron-withdrawing moiety, has high luminous efficiency. It was. As its manifestation mechanism, in the charge separation state in the excited state of the π-conjugated compound, the electron donating part is disposed away via the electron withdrawing part at the substitution position where the resonance structure can be obtained, It is presumed that the charge separation state can be stabilized with a wide π conjugate plane.

Schematic showing energy diagram of TADF compound Schematic diagram showing the energy diagram of a general fluorescent compound Schematic diagram showing the energy diagram when a π-conjugated compound functions as an assist dopant Schematic diagram showing the energy diagram when a π-conjugated compound functions as a host compound Schematic diagram showing an example of a display device composed of organic EL elements Schematic diagram of an active matrix display device Schematic showing the pixel circuit Schematic diagram of a passive matrix display device Schematic of lighting device Cross section of the lighting device

  Hereinafter, the present invention, its components, and modes and modes for carrying out the present invention will be described in detail. In addition, in this application, "-" is used in the meaning which includes the numerical value described before and behind that as a lower limit and an upper limit.

1. π-conjugated compound The π-conjugated compound of the present invention is a compound having a structure represented by the following general formula (1).

In the general formula (1), D ¹ and D ² existing in the para position are electron donating groups D.

M ^{1 to} M ⁴ each independently represent a nitrogen atom or —C—Z, and at least one of M ^{1 to} M ⁴ is a nitrogen atom. The compound of the present invention must have at least one nitrogen atom in the aromatic six-membered ring, but the number of nitrogen atoms is not particularly limited and is any one of 1 to 4.

When any of M ^{1 to} M ⁴ is —C—Z, Z is a hydrogen atom, a deuterium atom, or a substituent, and preferably an electron donating group D, an alkyl group, or an electron withdrawing group A.

(Electron donating group D)
The electron donating group D represented by Z in D ¹ and D ² or —C—Z is an “aryl group optionally substituted with an electron donating group” or “electron donating optionally substituted”. A "heterocyclic group" or "an optionally substituted amino group".

  The “aryl group” of the “aryl group optionally substituted with an electron donating group” represented by D is preferably an aryl group having 6 to 24 carbon atoms. Specifically, benzene ring, indene ring, naphthalene ring, azulene ring, fluorene ring, phenanthrene ring, anthracene ring, acenaphthylene ring, biphenylene ring, naphthacene ring, pyrene ring, pentalene ring, acanthrylene ring, heptalene ring, triphenylene Ring, as-indacene ring, chrysene ring, s-indacene ring, preaden ring, phenalene ring, fluoranthene ring, perylene ring, acephenanthrylene ring, biphenyl ring, terphenyl ring, tetraphenyl ring and the like. More preferably, a benzene ring, naphthalene ring, fluorene ring, phenanthrene ring, anthracene ring, biphenylene ring, chrysene ring, pyrene ring, triphenylene ring, chrysene ring, fluoranthene ring, perylene ring, biphenyl ring and terphenyl ring are mentioned.

  The “electron-donating heterocyclic group” of the “optionally substituted electron-donating heterocyclic group” represented by D is preferably a heterocyclic ring having 4 to 24 carbon atoms. Examples of such heterocyclic rings include pyrrole, indole, carbazole, azacarbazole, diazacarbazole, indoloindole, 9,10-dihydroacridine, 5,10-dihydrophenazacilline 10,11-dihydrodibenzazepine ring, phenoxazine ring, phenothiazine ring, dibenzothiophene ring, benzofurylindole ring, benzothienoindole ring, indolocarbazole ring, benzofurylcarbazole ring, benzothienocarbazole ring, benzothienobenzothiophene A ring, a benzocarbazole ring, a dibenzocarbazole ring, and the like. More preferably, a carbazole ring, an indoloindole ring, a 9,10-dihydroacridine ring, a phenoxazine ring, a phenothiazine ring, a dibenzothiophene ring, a benzofurylindole ring, and a benzocarbazole ring are exemplified. The above electron donating heterocycles may be combined by linking two or more of the same or different rings.

  The “electron-donating group” of the “aryl group substituted with an electron-donating group” represented by D includes an alkyl group, an alkoxy group, an optionally substituted amino group, and an optionally substituted electron donor. Sex heterocycles and the like. Preferably, the heterocyclic group of the alkyl group and the electron-donating group which may be substituted is mentioned.

  The “alkyl group” of the “electron-donating group” of the “aryl group substituted with an electron-donating group” represented by D may be linear, branched, or cyclic. 20 linear, branched, or cyclic alkyl groups may be mentioned, specifically, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, s-butyl group, t-butyl group, n-pentyl group, neopentyl group, n-hexyl group, cyclohexyl group, 2-ethylhexyl group, n-heptyl group, n-octyl group, 2-hexyloctyl group, n-nonyl group, n-decyl group, n-undecyl Group, n-dodecyl group, n-tridecyl group, n-tetradecyl group, n-pentadecyl group, n-hexadecyl group, n-heptadecyl group, n-octadecyl group, n-nonadecyl group and n-icosyl group. It is. Preferably, a methyl group, an ethyl group, an isopropyl group, a t-butyl group, a cyclohexyl group, a 2-ethylhexyl group, and a 2-hexyloctyl group are exemplified.

  The “alkoxy group” of the “electron-donating group” of the “aryl group substituted with an electron-donating group” represented by D may be linear, branched, or cyclic. 20 linear, branched, or cyclic alkyl groups may be mentioned. Specifically, methoxy group, ethoxy group, n-propoxy group, isopropoxy group, n-butoxy group, isobutoxy group, t-butoxy group, n -Pentyloxy group, neopentyloxy group, n-hexyloxy group, cyclohexyloxy group, n-heptyloxy group, n-octyloxy group, 2-ethylhexyloxy group, nonyloxy group, decyloxy group, 3,7-dimethyloctyl Oxy group, n-undecyloxy group, n-dodecyloxy group, n-tridecyloxy group, n-tetradecyloxy group, 2-n-hexyl-n Octyloxy group, n-pentadecyloxy group, n-hexadecyloxy group, n-heptadecyloxy group, n-octadecyloxy group, n-nonadecyloxy group, n-icosyloxy group, methoxy group, ethoxy group, An isopropoxy group, a t-butoxy group, a cyclohexyloxy group, a 2-ethylhexyloxy group, and a 2-hexyloctyloxy group are preferable.

  The substituent of the “optionally substituted amino group” of the “electron-donating group” of the “aryl group substituted with an electron-donating group” represented by D is an alkyl group or an alkyl group. An aryl ring which may be used is mentioned. Examples of the alkyl group and aryl group include the same ones as described above, and the same ones are preferable.

  Examples of the substituent of the “optionally substituted electron-donating heterocyclic group” represented by D include an alkyl group, an alkoxy group, an aryl ring which may be substituted with an alkyl group, and an optionally substituted group. An amino group etc. are mentioned, Specifically, the same thing as the above-mentioned is mentioned, The same thing is preferable.

  Examples of the “electron-donating heterocyclic group that may be substituted” of the “electron-donating group” of the “aryl group substituted with an electron-donating group” represented by D include the same groups as described above. Similar ones are preferred.

  Examples of the substituent of the “optionally substituted amino group” represented by D include the same as those described above, and the same is preferable.

  Examples of the “alkyl group” represented by Z in —C—Z include the same as those described above, and the same is preferable.

(Electron withdrawing group A)
The electron-withdrawing group A represented by Z in —C—Z is “fluorine atom”, “cyano group”, “alkyl group substituted with fluorine atom”, “optionally substituted carbonyl group”, “ “Optionally substituted sulfonyl group”, “optionally substituted phosphine oxide group”, “optionally substituted boryl group”, “optionally substituted aryl group (preferably an electron-withdrawing group) An optionally substituted aryl group), "or an" optionally withdrawing heterocyclic group ".

  Examples of the “alkyl group” of the “alkyl group substituted with a fluorine atom” represented by A include the same as those described above, and the same is preferable.

  Examples of the “aryl group” of the “optionally substituted aryl group” represented by A include the same as described above, and the same is preferable.

  The “heterocyclic group” of the “optionally substituted electron-withdrawing heterocyclic group” represented by A is preferably a heterocyclic group having 3 to 24 carbon atoms. Examples of such heterocyclic groups include dibenzothiophene oxide ring, dibenzothiophene dioxide ring, pyridine ring, pyridazine ring, pyrimidine ring, pyrazine ring, triazine ring, quinoline ring, isoquinoline ring, quinazoline ring, cinnoline ring, quinoxaline Ring, phthalazine ring, pteridine ring, phenanthridine ring, phenanthroline ring, dibenzofuran ring, dibenzosilole ring, dibenzoborol ring, dibenzophosphole oxide ring, azadibenzofuran ring, diazadibenzofuran ring and the like. More preferably, a pyridine ring, a pyrimidine ring, a pyrazine ring, a triazine ring, a quinoline ring, an isoquinoline ring, a quinazoline ring, a quinoxaline ring, a phenanthridine ring, a phenanthroline ring, a dibenzofuran ring, or a dibenzoborol oxide ring. The above heterocyclic group may be a combination of two or more rings that are the same or different.

  Examples of the substituent of the “electron-withdrawing heterocyclic group which may be substituted” represented by A include a deuterium atom, a fluorine atom, a cyano group, an alkyl group which may be substituted with a fluorine atom, a fluorine atom An aryl ring which may be substituted with an alkyl group which may be substituted with, or an aryl ring which may be substituted with a fluorine atom. Specific examples of the alkyl group and the aryl ring include the same ones as described above, and the same ones are preferable.

  Examples of the substituent of the “aryl group optionally substituted with an electron-withdrawing group” represented by A include a deuterium atom, a fluorine atom, a cyano group, an alkyl group optionally substituted with a fluorine atom, and a substituted group. An optionally substituted carbonyl group, an optionally substituted sulfonyl group, an optionally substituted phosphine oxide group, an optionally substituted boryl group, and an optionally substituted electron-withdrawing heterocyclic group. It is done.

  Among these, the substituent that the aryl group may have is preferably an electron-withdrawing group, and includes a fluorine atom, a cyano group, an alkyl group substituted with a fluorine atom, an optionally substituted carbonyl group, and a substituted group. Preferred sulfonyl group, optionally substituted phosphine oxide group, optionally substituted boryl group, optionally substituted electron-withdrawing heterocyclic group, preferably substituted by fluorine atom, cyano group, fluorine atom An alkyl group that is substituted or an electron-withdrawing heterocyclic group that may be substituted is more preferable.

  "Optionally substituted carbonyl group", "optionally substituted sulfonyl group", "optionally substituted phosphine oxide group", "optionally substituted boryl group" represented by A Examples of the substituent include a deuterium atom, a fluorine atom, a cyano group, an alkyl group that may be substituted with a fluorine atom, an aryl ring that may be substituted, and an electron-withdrawing heterocyclic ring that may be substituted. It is done. Specific examples include the same ones as described above, and the same ones are preferable.

  The π-conjugated compound of the present invention is preferably represented by any one of the following general formulas (2) to (21).

In general formulas (2) to (21), D ^{1 to} D ⁶ each independently represent an electron donating group D. Examples of the electron donating group D include the same ones as D ^{1 to} D ² in the general formula (1), and the same one is preferable.

In General Formulas (2) to (21), Z ^{1 to} Z ⁴ each independently represent a hydrogen atom, a deuterium atom, an alkyl group, or the electron-withdrawing group A. The electron-withdrawing group A is an electron-withdrawing group A that can be used as Z in the general formula (1), that is, a fluorine atom, a cyano group, an alkyl group substituted with a fluorine atom, an optionally substituted carbonyl group, A sulfonyl group that may be substituted, a phosphine oxide group that may be substituted, a boryl group that may be substituted, an aryl group that may be substituted with an electron-withdrawing group, or an electron that may be substituted It is an attractive heterocyclic group.

In general formulas (2) to (21), “alkyl group” represented by Z ^{1 to} Z ⁴ , “alkyl group substituted with fluorine atom”, “optionally substituted carbonyl group”, “substituted” Examples of the “optionally substituted sulfonyl group”, “optionally substituted phosphine oxide group”, and “optionally substituted boryl group” include those described above, and the same are preferable.

In the general formulas (2) to (21), examples of the “aryl group” in the “aryl group optionally substituted with an electron-withdrawing group” represented by Z ^{1 to} Z ⁴ include the same as those described above. Similar ones are preferred.

In the general formulas (2) to (21), the “electron-withdrawing heterocyclic group” of the “optionally substituted electron-withdrawing heterocyclic group” represented by Z ^{1 to} Z ⁴ is as described above. The same thing is mentioned, The same thing is preferable.

In the general formulas (2) to (21), examples of the substituent of the “optionally withdrawing heterocyclic group which may be substituted” represented by Z ^{1 to} Z ⁴ include a deuterium atom, a fluorine atom, and a cyano group. , An alkyl group substituted with a fluorine atom, an aryl ring optionally substituted with an alkyl group substituted with a fluorine atom, and an aryl ring optionally substituted with a fluorine atom. Specifically, the same thing as the above is mentioned, The same thing is preferable.

In the general formulas (2) to (21), the “electron withdrawing group” of the “aryl ring optionally substituted with an electron withdrawing group” represented by Z ^{1 to} Z ⁴ includes a fluorine atom and a cyano group. , An alkyl group substituted with a fluorine atom, an optionally substituted carbonyl group, an optionally substituted sulfonyl group, an optionally substituted phosphine oxide group, an optionally substituted boryl group, a substituted Represents an electron-withdrawing heterocyclic ring, and preferably includes a fluorine atom, a cyano group, an alkyl group which may be substituted with a fluorine atom, or an optionally substituted electron-withdrawing heterocyclic ring.

In the general formulas (2) to (21), the “electron withdrawing group” of the “aryl group optionally substituted with an electron withdrawing group” represented by A ^{1 to} A ⁴ is substituted with a fluorine atom. Alkyl group "," optionally substituted carbonyl group "," optionally substituted sulfonyl group "," optionally substituted phosphine oxide group "," optionally substituted boryl group ", Examples of the “optionally withdrawing electron-withdrawing heterocyclic group” include the same groups as described above, and the same groups are preferable.

In the π-conjugated compound having the structure represented by the general formulas (2) to (21), D ¹ = D ² = D ³ = D ⁴ = D ⁵ = D ⁶ and Z ¹ = Z ² = Z ³ = It is preferable to satisfy at least one of Z ⁴ . This is because not only the synthesis is relatively easy, but also good luminous efficiency is easily obtained.

In the π-conjugated compound having the structure represented by the general formula (1), the absolute value (ΔE _ST ) of the energy difference between the lowest excited singlet level and the lowest excited triplet level of the π-conjugated compound is It is preferable that it is 0.50 eV or less, and it is preferable to contain in the said organic electroluminescent element, the said element material, or the said luminescent thin film.

  Specific examples of preferred π-conjugated compounds according to the present invention are shown below. However, these compounds may further have a substituent or may have a structural isomer, and are limited to this description. Not.

By using these compounds, as described above, it is possible to enhance the electron donating property while suppressing the emission wavelength from becoming longer. The absolute value of Delta] E _ST of these compounds are for the following material 0.50EV, may exhibit TADF properties.

  Furthermore, since these compounds have bipolar properties and can cope with various energy levels, they can be used not only as a light emitting host but also as a compound suitable for hole transport and electron transport. Therefore, the present invention is not limited to use in a light emitting layer, and may be used for the above-described hole injection layer, hole transport layer, electron blocking layer, hole blocking layer, electron transport layer, electron injection layer, intermediate layer, and the like. .

<Synthesis method>
Examples of the π-conjugated compound include International Publication No. 2010/113755, Organic Letters, 2002, 4, 1783-1785. Or by referring to the methods described in the references described in these documents.

2. Organic Electroluminescence Element Material The π-conjugated compound having the structure represented by the general formula (1) can be used as an organic electroluminescence (EL) element material containing the π-conjugated compound. Specifically, the use of the π-conjugated compound having the structure represented by the general formula (1) as an organic electroluminescence element material for a light emitting material, a host material, an assist dopant, etc. From the viewpoint of sex.
Next, an organic EL light emitting system and a light emitting material related to the technical idea of the present invention will be described.

<Light emitting method of organic EL>
There are two types of organic EL emission methods: “phosphorescence emission” that emits light when returning from the triplet excited state to the ground state, and “fluorescence emission” that emits light when returning from the singlet excited state to the ground state. is there.

  When excited by an electric field such as an organic EL, triplet excitons are generated with a probability of 75% and singlet excitons are generated with a probability of 25%. Therefore, phosphorescence is more efficient than fluorescence. This is an excellent method for realizing low power consumption.

  On the other hand, in the fluorescence emission, the triplet excitons that are generated with a probability of 75% ordinarily, and the exciton energy becomes only heat due to non-radiation deactivation, are present at high density. There is a system using a TTA (triplet-triplet annealing: abbreviated as “TTF”) mechanism that generates singlet excitons from two triplet excitons to improve luminous efficiency. Has been found.

  Furthermore, in recent years, the discovery of Adachi et al. Has reduced the energy gap between the singlet excited state and the triplet excited state, so that the energy level of the triplet has a lower energy level due to the Joule heat during light emission and / or the environmental temperature where the light emitting element is placed. A phenomenon in which cross-reverse crossing occurs from a singlet excited state to a singlet excited state and, as a result, enables fluorescence emission nearly 100% (also referred to as thermally excited delayed fluorescence or thermally excited delayed fluorescence: “TADF”) A fluorescent substance that makes this possible has been found (see, for example, Non-Patent Document 1).

<Phosphorescent compound>
As described above, phosphorescence is theoretically 3 times more advantageous than fluorescence in terms of light emission efficiency, but energy deactivation (= phosphorescence) from triplet excited state to singlet ground state is forbidden. Similarly, since the intersystem crossing from the singlet excited state to the triplet excited state is also a forbidden transition, the rate constant is usually small. That is, since the transition is difficult to occur, the exciton lifetime is increased from millisecond to second order, and it is difficult to obtain desired light emission.

  However, when a complex using a heavy metal such as iridium or platinum emits light, the rate constant of the forbidden transition increases by 3 digits or more due to the heavy atom effect of the central metal. % Phosphorescence quantum yield can be obtained.

  However, in order to obtain such ideal light emission, it is necessary to use a rare metal called a white metal such as iridium, palladium, or platinum, which is a rare metal. The price of the metal itself is a major industrial issue.

<Fluorescent compound>
A general fluorescent compound is not necessarily a heavy metal complex like a phosphorescent compound, and is a so-called organic compound composed of a combination of general elements such as carbon, oxygen, nitrogen and hydrogen. In addition, other non-metallic elements such as phosphorus, sulfur, and silicon can be used, and complexes of typical metals such as aluminum and zinc can be used.

  However, since only 25% of excitons can be applied to light emission as described above with conventional fluorescent compounds, high efficiency light emission such as phosphorescence emission cannot be expected.

<Delayed fluorescent compound>
[Excited triplet-triplet annihilation (TTA) delayed fluorescent compound]
In order to solve the problems of fluorescent compounds, a light emission method using delayed fluorescence has appeared. The TTA method that originates from collisions between triplet excitons can be described by the following general formula. That is, there is a merit that a part of triplet excitons, in which the energy of excitons has been converted only to heat due to non-radiation deactivation, can cross back to singlet excitons that can contribute to light emission. Even in an actual organic EL device, it is possible to obtain an external extraction quantum efficiency approximately twice that of a conventional fluorescent light emitting device.
General formula: T ^* + T ^* → S ^* + S
(In the formula, T ^* represents a triplet exciton, S ^* represents a singlet exciton, and S represents a ground state molecule.)

  However, as can be seen from the above equation, since only one singlet exciton that can be used for light emission is generated from two triplet excitons, it is impossible in principle to obtain 100% internal quantum efficiency.

[Thermal activated delayed fluorescence (TADF) compound]
The TADF method, which is another highly efficient fluorescent emission, is a method that can solve the problems of TTA.

  As described above, the fluorescent compound has the advantage that the molecule can be designed infinitely. That is, among the molecularly designed compounds, there are compounds in which the energy level difference between the triplet excited state and the singlet excited state is extremely close.

Such compounds, even though in the molecule does not have a heavy atom, reverse intersystem crossing from a triplet excited state is usually not occur because Delta] E _ST is smaller to the singlet excited state occurs. Furthermore, since the rate constant of deactivation from singlet excited state to ground state (= fluorescence emission) is extremely large, triplet excitons themselves are thermally deactivated to ground state (non-radiative deactivation). It is more kinetically advantageous to return to the ground state while emitting fluorescence via the singlet excited state. Therefore, TADF theoretically enables 100% fluorescence emission.

<Molecular design concepts related to ΔE _ST>
It explained molecular design for reducing the Delta] E _ST.
ΔE in order to reduce the _ST is highest occupied molecular orbital in principle molecules (Highest Occupied Molecular Orbital: HOMO) and lowest unoccupied molecular orbital (Lowest Unoccupied Molecular Orbital: LUMO) spatial overlap the small to most effects of Is.

  In general, it is known that HOMO is distributed in electron donating sites and LUMO is distributed in electron withdrawing sites in the electron orbit of the molecule. By introducing an electron donating and electron withdrawing skeleton into the molecule, HOMO is distributed. It is possible to move away the position where LUMO exists.

  For example, in "Organic optoelectronics at the stage of practical application", Vol. 82, No. 6, 2013, electron-withdrawing skeletons such as cyano groups and triazines and electron donations such as carbazole and diphenylamino groups By introducing a sex skeleton, LUMO and HOMO are localized.

  It is also effective to reduce the change in molecular structure between the ground state and triplet excited state of the compound. As a method for reducing the structural change, for example, making the compound rigid is effective. Rigidity described here means that there are few sites that can move freely in the molecule, for example, by suppressing free rotation in the bond between the rings in the molecule or by introducing a condensed ring with a large π conjugate plane. means. In particular, it is possible to reduce the structural change in the excited state by making the portion involved in light emission rigid.

<General problems with TADF compounds>
TADF compounds have various problems in terms of their light emission mechanism and molecular structure. The following describes some of the problems generally associated with TADF compounds.

In TADF compound, it is necessary to release as possible sites present in the HOMO and LUMO in order to reduce the Delta] E _ST, Therefore, the electronic state of the molecule of the donor / acceptor type HOMO site and LUMO sites separated It becomes a state close to intramolecular CT (intramolecular charge transfer state).

  When a plurality of such molecules are present, stabilization is achieved by bringing the donor part of one molecule and the acceptor part of the other molecule close to each other. Such a stabilization state is not limited to the formation between two molecules, but can also be formed between a plurality of molecules such as three or five molecules. As a result, various stabilization states with a wide distribution are obtained. As a result, the shape of the absorption spectrum and emission spectrum becomes broad. In addition, even when a multimolecular assembly exceeding two molecules is not formed, various existence states can be taken depending on the direction and angle of interaction between the two molecules. The shape of the emission spectrum becomes broad.

  The broad emission spectrum creates two major problems. One problem is that the color purity of the emitted color is lowered. This is not a big problem when applied to lighting applications, but when used for electronic displays, the color gamut is small and the color reproducibility of pure colors is low. It becomes difficult.

Another problem is the rising wavelength on the short wavelength side of the emission spectrum (referred to as "fluorescent 0-0 band".) To reduce the wavelength, i.e. higher S ₁ (higher energy of the lowest excited singlet energy level) It is to do.

Naturally, when the wavelength of the fluorescent 0-0 band is shortened, the phosphorescent 0-0 band derived from T ₁ having lower energy than S ₁ is also shortened (increased T ₁ level). Therefore, the compound used for the host compound needs to have a high S ₁ level and a high T ₁ level in order to prevent reverse energy transfer from the dopant.

  This is a very big problem. A host compound consisting essentially of an organic compound takes a plurality of active and unstable chemical species such as a cation radical state, an anion radical state, and an excited state in an organic EL device. By expanding the π-conjugated system, it can exist relatively stably.

However, in order to impart a high S ₁ level and a high T ₁ level to a molecule, it is necessary to reduce or cut off the π-conjugated system in the molecule, making it difficult to achieve both stability and As a result, the lifetime of the light emitting element is shortened.

In addition, in a TADF compound that does not contain a heavy metal, a transition that is deactivated from a triplet excited state to a ground state is a forbidden transition, and therefore the existence time (exciton lifetime) in the triplet excited state is from several hundred microseconds to millisecond. It is very long with second order. For this reason, even if the T ₁ energy level of the host compound is higher than that of the fluorescent compound, the triplet excited state of the fluorescent compound from the triplet excited state to the host compound is determined from the length of the existence time. The probability of causing reverse energy transfer increases. As a result, the reverse reverse energy transfer from the triplet excited state to the singlet excited state of the originally intended TADF compound does not occur sufficiently, and unfavorable reverse energy transfer to the host compound becomes the mainstream, resulting in sufficient luminous efficiency. Inconvenience that cannot be obtained.

  In order to solve the above problems, it is necessary to sharpen the emission spectrum shape of the TADF compound and reduce the difference between the emission maximum wavelength and the rising wavelength of the emission spectrum. This can be basically achieved by reducing the change in the molecular structure of the singlet excited state and the triplet excited state.

  In order to suppress reverse energy transfer to the host compound, it is effective to shorten the existence time (exciton lifetime) of the triplet excited state of the TADF compound. To achieve this, it is necessary to take measures such as reducing the molecular structure change between the ground state and the triplet excited state and introducing suitable substituents and elements to undo the forbidden transition. Can be solved.

  Hereinafter, various measurement methods relating to the π-conjugated compound according to the present invention will be described.

[Electron density distribution]
Π conjugated compound according to the present invention, from the viewpoint of reducing the Delta] E _ST, it is preferable that HOMO and LUMO are substantially separated in the molecule. The distribution states of these HOMO and LUMO can be obtained from the electron density distribution when the structure is optimized by molecular orbital calculation.

  In the present invention, the structure optimization and the calculation of the electron density distribution by molecular orbital calculation of the π-conjugated compound in the present invention are performed by using molecular orbital calculation software using B3LYP as a functional and 6-31G (d) as a basis function as a calculation method. There is no particular limitation on the software, and any of them can be similarly calculated.

  In the present invention, Gaussian 09 (Revision C.01, MJ Frisch, et al, Gaussian, Inc., 2010.) manufactured by Gaussian, USA was used as molecular orbital calculation software.

  Further, “HOMO and LUMO are substantially separated” means that the HOMO orbital distribution calculated by the above molecular calculation and the central part of the LUMO orbital distribution are separated, more preferably the HOMO orbital distribution and the LUMO orbital. This means that the distributions of do not overlap.

As for the separation state of HOMO and LUMO, from the above-described structure optimization calculation using B3LYP as the functional and 6-31G (d) as the basis function, the time-dependent density functional method (Time-Dependent DFT) is used. The excited state calculation is performed to obtain the energy levels of S ₁ and T ₁ (E (S ₁ ) and E (T ₁ ), respectively), and ΔE _ST = | E (S ₁ ) −E (T ₁ ) | It is also possible to calculate. As calculated Delta] E _ST is small, indicating that the HOMO and LUMO are more separated. In the present invention, it is Delta] E _ST calculated using the calculation method similar to that described above or less 0.50EV, preferably not more than 0.30 eV, more preferably not more than 0.10 eV.

[Lowest excitation singlet energy level S ₁ ]
The lowest excited singlet energy level S ₁ of the π-conjugated compound in the present invention is defined in the present invention as calculated in the same manner as in a normal method. That is, a sample to be measured is deposited on a quartz substrate to prepare a sample, and the absorption spectrum (vertical axis: absorbance, horizontal axis: wavelength) of this sample is measured at room temperature (300 K). A tangent line is drawn with respect to the rising edge of the absorption spectrum on the long wavelength side, and is calculated from a predetermined conversion formula based on the wavelength value at the intersection of the tangent line and the horizontal axis.

However, when the molecules themselves of the π-conjugated compound used in the present invention have a relatively high aggregation property, an error due to aggregation may occur in the measurement of the thin film. In consideration of the fact that the π-conjugated compound in the present invention has a relatively small Stokes shift and that the structural change between the excited state and the ground state is small, the lowest excited singlet energy level S ₁ in the present invention is room temperature (25 ° C. The peak value of the maximum emission wavelength in the solution state of the π-conjugated compound in (1) was used as an approximate value.

  Here, as the solvent to be used, a solvent that does not affect the aggregation state of the π-conjugated compound, that is, a solvent having a small influence of the solvent effect, for example, a nonpolar solvent such as cyclohexane or toluene can be used.

[Lowest excited triplet energy level T ₁ ]
The lowest excited triplet energy level (T ₁ ) of the π-conjugated compound used in the present invention was calculated from the photoluminescence (PL) characteristics of the solution or thin film. For example, as a calculation method in a thin film, after making a dispersion of a dilute π-conjugated compound into a thin film, using a streak camera, the transient PL characteristics are measured to separate the fluorescent component and the phosphorescent component, the absolute value of the energy difference can be determined the lowest excited triplet energy level of the lowest excited singlet energy level as Delta] E _ST.

  In measurement / evaluation, an absolute PL quantum yield measurement apparatus C9920-02 (manufactured by Hamamatsu Photonics) was used for measurement of the absolute PL quantum yield. The light emission lifetime was measured using a streak camera C4334 (manufactured by Hamamatsu Photonics) while exciting the sample with laser light.

3. Organic EL Element The organic EL element of the present invention is an organic electroluminescence element having at least a light emitting layer between an anode and a cathode, and at least one layer of the light emitting layer is represented by the general formula (1). It contains a π-conjugated compound having

As typical element structures in the organic EL element of the present invention, the following structures can be exemplified, but the invention is not limited thereto.
(1) Anode / light emitting layer / cathode (2) Anode / light emitting layer / electron transport layer / cathode (3) Anode / hole transport layer / light emitting layer / cathode (4) Anode / hole transport layer / light emitting layer / electron Transport layer / cathode (5) Anode / hole transport layer / light emitting layer / electron transport layer / electron injection layer / cathode (6) Anode / hole injection layer / hole transport layer / light emitting layer / electron transport layer / cathode ( 7) Anode / hole injection layer / hole transport layer / (electron blocking layer /) luminescent layer / (hole blocking layer /) electron transport layer / electron injection layer / cathode Among the above, the configuration of (7) is preferable. Although used, it is not limited to this.

  The light emitting layer used in the present invention is composed of a single layer or a plurality of layers. When there are a plurality of light emitting layers, a non-light emitting intermediate layer may be provided between the light emitting layers.

  If necessary, a hole blocking layer (also referred to as a hole blocking layer) or an electron injection layer (also referred to as a cathode buffer layer) may be provided between the light emitting layer and the cathode. An electron blocking layer (also referred to as an electron barrier layer) or a hole injection layer (also referred to as an anode buffer layer) may be provided therebetween.

  The electron transport layer used in the present invention is a layer 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. Moreover, you may be comprised by multiple layers.

  The hole transport layer used in the present invention is a layer 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. Moreover, you may be comprised by multiple layers.

  In the above-described typical element configuration, the layer excluding the anode and the cathode is also referred to as “organic layer”.

(Tandem structure)
The organic EL element of the present invention may be a so-called tandem element in which a plurality of light emitting units including at least one light emitting layer are stacked.

As typical element configurations of the tandem structure, for example, the following configurations can be given.
Anode / first light emitting unit / intermediate layer / second light emitting unit / intermediate layer / third light emitting unit / cathode

  Here, the first light emitting unit, the second light emitting unit, and the third light emitting unit may all be the same or different. Two light emitting units may be the same, and the remaining one may be different.

  A plurality of light emitting units may be laminated directly or via an intermediate layer, and the intermediate layer is generally an intermediate electrode, an intermediate conductive layer, a charge generation layer, an electron extraction layer, a connection layer, an intermediate layer. A known material structure can be used as long as it is also called an insulating layer and has a function of supplying electrons to the anode-side adjacent layer and holes to the cathode-side adjacent layer.

Examples of materials used for the intermediate layer include ITO (indium tin oxide), IZO (indium zinc oxide), ZnO ₂ , TiN, ZrN, HfN, TiOx, VOx, CuI, InN, GaN, CuAlO ₂ , Conductive inorganic compound layers such as CuGaO ₂ , SrCu ₂ O ₂ , LaB ₆ , RuO ₂ and Al, two-layer films such as Au / Bi ₂ O ₃ , SnO ₂ / Ag / SnO ₂ , ZnO / Ag / ZnO , Bi ₂ O ₃ / Au / Bi ₂ O ₃ , TiO ₂ / TiN / TiO ₂ , TiO ₂ / ZrN / TiO _{2 and} other multilayer films, C _{60 and} other fullerenes, conductive organic layers such as oligothiophene, Examples include conductive organic compound layers such as metal phthalocyanines, metal-free phthalocyanines, metal porphyrins, metal-free porphyrins, etc. The invention is not limited to these.

  As a preferable configuration in the light emitting unit, for example, a configuration in which the anode and the cathode are excluded from the configurations (1) to (7) described in the above-described typical element configurations, and the like is described. It is not limited.

  Specific examples of the tandem organic EL element include, for example, US Pat. No. 6,337,492, US Pat. No. 7,420,203, US Pat. No. 7,473,923, US Pat. No. 6,872,472, US Pat. No. 6,107,734, US Pat. No. 6,337,492, International JP 2005/009087, JP 2006-228712, JP 2006-24791, JP 2006-49393, JP 2006-49394, JP 2006-49396, JP 2011. No. -96679, JP 2005-340187, JP 47114424, JP 34096681, JP 3884564, JP 431169, JP 2010-192719, JP 2009-076929, JP Open 2008-0784 No. 4, JP 2007-059848 A, JP 2003-272860 A, JP 2003-045676 A, International Publication No. 2005/094130, and the like. The present invention is not limited to these.

  Hereinafter, each layer which comprises the organic EL element of this invention is demonstrated.

(Light emitting layer)
The light-emitting layer used in the present invention is a layer that provides a field in which electrons and holes injected from an electrode or an adjacent layer are recombined to emit light via excitons, and the light-emitting portion is the light-emitting layer. Even in the layer, it may be the interface between the light emitting layer and the adjacent layer. If the light emitting layer used for this invention satisfy | fills the requirements prescribed | regulated by this invention, there will be no restriction | limiting in particular in the structure.

  The total thickness of the light emitting layer is not particularly limited, but it prevents the uniformity of the film to be formed, the application of unnecessary high voltage during light emission, and the improvement of the stability of the emission color against the drive current. From a viewpoint, it is preferable to adjust to the range of 2 nm-5 micrometers, More preferably, it adjusts to the range of 2-500 nm, More preferably, it adjusts to the range of 5-200 nm.

  Further, the thickness of each light emitting layer used in the present invention is preferably adjusted to a range of 2 nm to 1 μm, more preferably adjusted to a range of 2 to 200 nm, and further preferably in a range of 3 to 150 nm. Adjusted.

  The light emitting layer used in the present invention may be a single layer or a plurality of layers. When the π-conjugated compound of the present application is used for the light emitting layer, it may be used alone or in combination with a host material, a fluorescent light emitting material, a phosphorescent light emitting material, etc. described later. At least one layer of the light emitting layer contains a light emitting dopant (a light emitting compound, a light emitting dopant, also simply referred to as a dopant), and further contains a host compound (a matrix material, a light emitting host compound, also simply referred to as a host). preferable. In the π-conjugated compound of the present application, it is preferable that at least one layer of the light-emitting layer contains the π-conjugated compound of the present application and a host compound because luminous efficiency is improved. It is preferable that at least one layer of the light-emitting layer contains the π-conjugated compound of the present application and at least one of a fluorescent compound and a phosphorescent compound because luminous efficiency is improved. It is preferable that at least one layer of the light emitting layer contains the present π-conjugated compound, at least one of a fluorescent light emitting compound and a phosphorescent light emitting compound, and a host compound because the light emission efficiency is improved.

(1.1) Luminescent dopant As the luminescent dopant, a fluorescent luminescent dopant (also referred to as a fluorescent luminescent compound or a fluorescent dopant) and a phosphorescent dopant (also referred to as a phosphorescent luminescent compound or a phosphorescent dopant) are used. Preferably used. In the present invention, the light emitting layer contains the π-conjugated compound according to the present invention in the range of 0.1 to 50% by mass as a fluorescent compound or assist dopant, and particularly in the range of 1 to 30% by mass. It is preferable to contain within.

  In this invention, it is preferable that a light emitting layer contains a luminescent compound in the range of 0.1-50 mass%, and contains in the range of 1-30 mass% especially.

  The concentration of the light-emitting compound in the light-emitting layer can be arbitrarily determined based on the specific light-emitting compound used and the requirements of the device, and is uniform in the thickness direction of the light-emitting layer. It may be contained and may have any concentration distribution.

  In addition, the luminescent compound used in the present invention may be used in combination of two or more kinds, a combination of fluorescent luminescent compounds having different structures, or a combination of a fluorescent luminescent compound and a phosphorescent luminescent compound. May be. Thereby, arbitrary luminescent colors can be obtained.

The absolute value (ΔE _ST ) of the difference between the lowest excited singlet energy level and the lowest excited triplet energy level is 0.50 eV or less, a π-conjugated compound according to the present invention, a luminescent compound, and a host compound. When contained in the light emitting layer, the π-conjugated compound according to the present invention acts as an assist dopant. On the other hand, when the light emitting layer contains the π-conjugated compound and the luminescent compound according to the present invention and does not contain the host compound, the π-conjugated compound according to the present invention acts as a host compound. When the light emitting layer contains only the π-conjugated compound according to the present invention, the π-conjugated compound according to the present invention acts as a host compound / light-emitting compound.

  The mechanism for producing the effect is the same in any case, and the triplet exciton generated on the π-conjugated compound according to the present invention is converted into a singlet exciton by reverse intersystem crossing (RISC). It is in.

  As a result, all the exciton energies generated on the π-conjugated compound according to the present invention can be transferred to the luminescent compound by fluorescence resonance energy transfer (FRET), thereby realizing high luminous efficiency.

Therefore, when the light emitting layer contains the three components of the π-conjugated compound, the luminescent compound, and the host compound according to the present invention, the energy levels of S ₁ and T ₁ of the π-conjugated compound are S of the host compound. ₁ and T ₁ of the lower than the energy level, it is preferably higher than the energy level of the S ₁ and T ₁ of the light-emitting compound.

Similarly, light emitting layer, the energy level of the S ₁ and T ₁ of the case containing the two components of the light emitting compound and [pi conjugated compound according to the present invention, [pi-conjugated compounds, S ₁ luminescent compound higher than the energy level of T ₁ and is preferable.

  FIG. 3 and FIG. 4 show schematic diagrams when the π-conjugated compound of the present invention acts as an assist dopant and a host compound, respectively. 3 and 4 are examples, and the generation process of the triplet exciton generated on the π-conjugated compound according to the present invention is not limited to the electric field excitation, and the energy transfer from the light emitting layer or the peripheral layer interface. And electronic transfer.

  Further, in FIGS. 3 and 4, a fluorescent compound is used as a light-emitting material, but the present invention is not limited to this, and a phosphorescent compound may be used, or a fluorescent compound and a phosphorescent compound may be used. Both of the functional compounds may be used.

  When the π-conjugated compound according to the present invention is used as an assist dopant, the light-emitting layer contains a host compound in a mass ratio of 100% or more with respect to the π-conjugated compound, and the fluorescent compound and / or phosphorescent compound. Is preferably contained within a range of 0.1 to 50% by mass with respect to the π-conjugated compound.

  In the case where the π-conjugated compound according to the present invention is used as a host compound, the light emitting layer has a mass ratio of 0.1 to 50% of the fluorescent compound and / or the phosphorescent compound with respect to the π-conjugated compound. It is preferable to contain.

  When the π-conjugated compound according to the present invention is used as an assist dopant or host compound, it is preferable that the emission spectrum of the π-conjugated compound according to the present invention and the absorption spectrum of the luminescent compound overlap.

  The light emission color of the organic EL device of the present invention and the compound used in the present invention is shown in FIG. 3.16 on page 108 of “New Color Science Handbook” (edited by the Japan Color Society, University of Tokyo Press, 1985). It is determined by the color when the result measured with the luminance meter CS-1000 (manufactured by Konica Minolta Co., Ltd.) is applied to the CIE chromaticity coordinates.

  In the present invention, it is also preferable that the light emitting layer of one layer or a plurality of layers contains a plurality of light emitting dopants having different emission colors and emits white light.

  There are no particular limitations on the combination of light-emitting dopants that exhibit white, and examples include blue and orange, and a combination of blue, green, and red.

The white color in the organic EL device of the present invention means that the chromaticity in the CIE 1931 color system at 1000 cd / m ² is x = 0.39 ± 0.09 when the 2 ° viewing angle front luminance is measured by the method described above. Y = 0.38 ± 0.08.

(1.2) Fluorescent Luminescent Dopant As the fluorescent luminescent dopant (fluorescent dopant), the π-conjugated compound of the present invention may be used, or a known fluorescent dopant or delayed fluorescence used in the light emitting layer of the organic EL device. You may use it, selecting suitably from sex dopant.

  Specific examples of known fluorescent dopants that can be used in the present invention include, for example, anthracene derivatives, pyrene derivatives, chrysene derivatives, fluoranthene derivatives, perylene derivatives, fluorene derivatives, arylacetylene derivatives, styrylarylene derivatives, styrylamine derivatives, arylamine derivatives. , Boron complexes, coumarin derivatives, pyran derivatives, cyanine derivatives, croconium derivatives, squalium derivatives, oxobenzanthracene derivatives, fluorescein derivatives, rhodamine derivatives, pyrylium derivatives, perylene derivatives, polythiophene derivatives, rare earth complex compounds, and the like. In recent years, light emitting dopants utilizing delayed fluorescence have been developed, and these may be used. Specific examples of the luminescent dopant using delayed fluorescence include, for example, compounds described in International Publication No. 2011/156793, Japanese Patent Application Laid-Open No. 2011-213643, Japanese Patent Application Laid-Open No. 2010-93181, Japanese Patent No. 5366106, and the like. However, the present invention is not limited to these.

(1.3) Phosphorescent dopant The phosphorescent dopant used in the present invention will be described.
The phosphorescent dopant used in the present invention is a compound in which light emission from an excited triplet is observed, specifically, a compound that emits phosphorescence at room temperature (25 ° C.), and a phosphorescence quantum yield. Is defined as a compound of 0.01 or more at 25 ° C., but a preferable phosphorescence quantum yield is 0.1 or more.

  The phosphorescence quantum yield can be measured by the method described in Spectroscopic II, page 398 (1992 edition, Maruzen) of Experimental Chemistry Course 4 of the 4th edition. Although the phosphorescence quantum yield in a solution can be measured using various solvents, the phosphorescence dopant used in the present invention achieves the phosphorescence quantum yield (0.01 or more) in any solvent. Just do it.

  The phosphorescent dopant can be appropriately selected from known materials used for the light emitting layer of the organic EL device. Specific examples of known phosphorescent dopants that can be used in the present invention include compounds described in the following documents.

  Nature 395, 151 (1998), Appl. Phys. Lett. 78, 1622 (2001), Adv. Mater. 19, 739 (2007), Chem. Mater. 17, 3532 (2005), Adv. Mater. 17, 1059 (2005), International Publication No. 2009/100991, International Publication No. 2008/101842, International Publication No. 2003/040257, US Patent Application Publication No. 2006/835469, US Patent Application Publication No. 2006 /. No. 0202194, U.S. Patent Application Publication No. 2007/0087321, U.S. Patent Application Publication No. 2005/0244673, Inorg. Chem. 40, 1704 (2001), Chem. Mater. 16, 2480 (2004), Adv. Mater. 16, 2003 (2004), Angew. Chem. lnt. Ed. 2006, 45, 7800, Appl. Phys. Lett. 86, 153505 (2005), Chem. Lett. 34, 592 (2005), Chem. Commun. 2906 (2005), Inorg. Chem. 42, 1248 (2003), International Publication No. 2009/050290, International Publication No. 2002/015645, International Publication No. 2009/000673, US Patent Application Publication No. 2002/0034656, US Pat. No. 7,332,232, US Patent Application Publication No. 2009/0108737, United States Patent Application Publication No. 2009/0039776, United States Patent No. 6921915, United States Patent No. 6,687,266, United States Patent Application Publication No. 2007/0190359, United States Patent Application Publication No. 2006/0008670, United States Patent Application Publication No. 2009/0165846, United States Patent Application Publication No. 2008/0015355, United States Patent No. 7250226, United States Patent No. 7396598, United States Patent Application Publication No. 2006 0263635 Pat, U.S. Patent Application Publication No. 2003/0138657, U.S. Patent Application Publication No. 2003/0152802, U.S. Patent No. 7090928, Angew. Chem. lnt. Ed. 47, 1 (2008), Chem. Mater. 18, 5119 (2006), Inorg. Chem. 46, 4308 (2007), Organometallics 23, 3745 (2004), Appl. Phys. Lett. 74, 1361 (1999), International Publication No. 2002/002714, International Publication No. 2006/009024, International Publication No. 2006/056418, International Publication No. 2005/019373, International Publication No. 2005/123873, International Publication No. 2005/123873, International Publication No. 2007/004380, International Publication No. 2006/082742, US Patent Application Publication No. 2006/0251923, US Patent Application Publication No. 2005/0260441, US Pat. No. 7,393,599. , US Pat. No. 7,534,505, US Pat. No. 7,445,855, US Patent Application Publication No. 2007/0190359, US Patent Application Publication No. 2008/0297033, US Pat. No. 7,338,722, US Patent Application Publication No. 2002 / 0 No. 34984, U.S. Pat. No. 7,279,704, U.S. Patent Application Publication No. 2006/098120, U.S. Patent Application Publication No. 2006/103874, WO 2005/076380, WO 2010/032663. International Publication No. 2008140115, International Publication No. 2007/052431, International Publication No. 2011/134013, International Publication No. 2011/157339, International Publication No. 2010/086089, International Publication No. 2009/113646, International Publication No. 2012/020327, International Publication No. 2011/051404, International Publication No. 2011/004639, International Publication No. 2011/073149, US Patent Application Publication No. 2012/228583, US Patent Application Publication No. 2012/21211. No. 6, JP 2012-069737 A, Japanese Patent Application No. 2011-181303, JP 2009-114086, JP 2003-81988, JP 2002-302671, JP 2002-363552. Gazette.

  Among these, a preferable phosphorescent dopant includes an organometallic complex having Ir as a central metal. More preferably, a complex containing at least one coordination mode of a metal-carbon bond, a metal-nitrogen bond, a metal-oxygen bond, or a metal-sulfur bond is preferable.

(2) Host compound The host compound used in the present invention is a compound mainly responsible for charge injection and transport in the light emitting layer, and its own light emission is not substantially observed in the organic EL device.

  The host compound preferably has a mass ratio in the layer of 20% or more among the compounds contained in the light emitting layer.

  A host compound may be used independently or may be used in combination of multiple types. By using a plurality of types of host compounds, it is possible to adjust the movement of charges, and the efficiency of the organic electroluminescence element can be improved.

  The host compound that is preferably used in the present invention will be described below.

  As the host compound, the π-conjugated compound used in the present invention may be used as described above, but there is no particular limitation. From the viewpoint of reverse energy transfer, those having an excitation energy larger than the excitation singlet energy of the dopant are preferred, and those having an excitation triplet energy larger than the excitation triplet energy of the dopant are more preferred.

  The host compound is responsible for carrier transport and exciton generation in the light emitting layer. Therefore, it can exist stably in all active species states such as cation radical state, anion radical state, and excited state, and does not cause chemical changes such as decomposition and addition reaction. It is preferable not to move at the angstrom level.

In particular, when the luminescent dopant used in combination exhibits TADF emission, the existence time of the triplet excited state of the TADF compound is long, so that the T ₁ energy level of the host compound itself is high, and the host compounds are associated with each other. Molecules in which the host compound does not decrease in T ₁ , such as not forming a low T ₁ state in the state, TADF compound and the host compound do not form an exciplex, or the host compound does not form an electromer due to an electric field. Appropriate design of the structure is required.

In order to satisfy these requirements, the host compound itself must have high electron hopping mobility, high hole hopping movement, and small structural change when it is in a triplet excited state. It is. Preferred examples of host compounds that satisfy such requirements include those having a high T ₁ energy level, such as a carbazole skeleton, an azacarbazole skeleton, a dibenzofuran skeleton, a dibenzothiophene skeleton, or an azadibenzofuran skeleton.

  In addition, the host compound has a hole transporting ability or an electron transporting ability, prevents the emission of light from becoming longer, and further stabilizes the organic electroluminescence device against heat generation during high temperature driving or during device driving. From the viewpoint of operating, it is preferable to have a high glass transition temperature (Tg). Tg is preferably 90 ° C. or higher, more preferably 120 ° C. or higher.

  Here, the glass transition point (Tg) is a value obtained by a method based on JIS K 7121-2012 using DSC (Differential Scanning Colorimetry).

As the host compound used in the present invention, it is also preferable to use the π-conjugated compound according to the present invention as described above. The π-conjugated compound according to the present invention has a high T ₁ and can be suitably used for a light-emitting material having a short emission wavelength (that is, a high energy level of T ₁ and S ₁ ). It is.

  When a known host compound is used in the organic EL device of the present invention, specific examples thereof include compounds described in the following documents, but the present invention is not limited thereto.

  JP-A-2001-257076, 2002-308855, 2001-313179, 2002-319491, 2001-357777, 2002-334786, 2002-8860, 2002-334787, 2002-15871, 2002-334788, 2002-43056, 2002-334789, 2002-75645, 2002-338579, 2002-105445 gazette, 2002-343568 gazette, 2002-141173 gazette, 2002-352957 gazette, 2002-203683 gazette, 2002-363227 gazette, 2002-231453 gazette, No. 003-3165, No. 2002-234888, No. 2003-27048, No. 2002-255934, No. 2002-286061, No. 2002-280183, No. 2002-299060, No. 2002. -302516, 2002-305083, 2002-305084, 2002-308837, U.S. Patent Application Publication No. 2003/0175553, U.S. Patent Application Publication No. 2006/0280965, U.S. Patent Application Publication. 2005/0112407, U.S. Patent Publication No. 2009/0017330, U.S. Patent Application Publication No. 2009/0030202, U.S. Patent Application Publication No. 2005/0238919, International Publication No. 2001/039234, International Publication No. 20 9/021126, International Publication No. 2008/056746, International Publication No. 2004/093207, International Publication No. 2005/089025, International Publication No. 2007/063796, International Publication No. 2007/063754, International Publication No. 2004 / 107822, International Publication No. 2005/030900, International Publication No. 2006/114966, International Publication No. 2009/086028, International Publication No. 2009/003898, International Publication No. 2012/023947, Japanese Patent Application Laid-Open No. 2008-074939. JP 2007-254297 A, European Patent No. 2034538, International Publication No. 2011/055933, International Publication No. 2012/035853, Japanese Unexamined Patent Publication No. 2015-38941, and the like. Examples thereof include compounds H-1 to H-230 described in paragraphs 0255 to 0293 of JP-A-2015-38941 and the following compounds H-231 to H-234.

(Electron transport layer)
In the present invention, the electron transport layer is made of a material having a function of transporting electrons, and may have a function of transmitting electrons injected from the cathode to the light emitting layer.

  Although there is no restriction | limiting in particular about the total layer thickness of the electron carrying layer which concerns on this invention, Usually, it is the range of 2 nm-5 micrometers, More preferably, it is 2-500 nm, More preferably, it is 5-200 nm.

  Further, in the organic EL element, when the light generated in the light emitting layer is extracted from the electrode, the light extracted directly from the light emitting layer interferes with the light extracted after being reflected by the electrode from which the light is extracted and the electrode located at the counter electrode. It is known to wake up. When light is reflected by the cathode, this interference effect can be efficiently utilized by appropriately adjusting the total thickness of the electron transport layer between several nanometers and several micrometers.

On the other hand, when the layer thickness of the electron transport layer is increased, the voltage is likely to increase. Therefore, particularly when the layer thickness is thick, the electron mobility of the electron transport layer is preferably 10 ⁻⁵ cm ² / Vs or more. .

  The material used for the electron transport layer (hereinafter referred to as an electron transport material) may be any of electron injecting or transporting properties and hole blocking properties, and can be selected from conventionally known compounds. Can be selected and used.

  For example, nitrogen-containing aromatic heterocyclic derivatives (carbazole derivatives, azacarbazole derivatives (one or more carbon atoms constituting the carbazole ring are substituted with nitrogen atoms), pyridine derivatives, pyrimidine derivatives, pyrazine derivatives, pyridazine derivatives, Triazine derivatives, quinoline derivatives, quinoxaline derivatives, phenanthroline derivatives, azatriphenylene derivatives, oxazole derivatives, thiazole derivatives, oxadiazole derivatives, thiadiazole derivatives, triazole derivatives, benzimidazole derivatives, benzoxazole derivatives, benzthiazole derivatives, etc.), dibenzofuran derivatives, Dibenzothiophene derivatives, silole derivatives, aromatic hydrocarbon ring derivatives (naphthalene derivatives, anthracene derivatives, triphenylene derivatives, etc.) That.

  In addition, a metal complex having a quinolinol skeleton or a dibenzoquinolinol skeleton as a ligand, for example, 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) and the like, and their metal complexes A metal complex in which the central metal is replaced with In, Mg, Cu, Ca, Sn, Ga, or Pb can also be used as the 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 transport 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 an inorganic semiconductor such as n-type-Si, n-type-SiC, etc. as in the case of the hole injection layer and the hole transport layer. Can also be used as an electron transporting material.

  Further, 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 the electron transport layer according to the present invention, the electron transport layer may be doped with a doping material as a guest material to form an electron transport layer having a high n property (electron rich). Examples of the doping material include n-type dopants such as metal complexes and metal compounds such as metal halides. Specific examples of the electron transport layer having such a structure include, for example, JP-A-4-297076, JP-A-10-270172, JP-A-2000-196140, 2001-102175, J. Pat. Appl. Phys. , 95, 5773 (2004) and the like.

  Specific examples of known preferable electron transport materials used in the organic EL device of the present invention include compounds described in the following documents, but the present invention is not limited thereto.

  US Pat. No. 6,528,187, US Pat. No. 7,230,107, US Patent Application Publication No. 2005/0025993, US Patent Application Publication No. 2004/0036077, US Patent Application Publication No. 2009/0115316, US Patent Application Publication No. 2009/0101870, United States Patent Application Publication No. 2009/0179554, International Publication No. 2003/060956, International Publication No. 2008/132805, Appl. Phys. Lett. 75, 4 (1999), Appl. Phys. Lett. 79, 449 (2001), Appl. Phys. Lett. 81, 162 (2002), Appl. Phys. Lett. 81, 162 (2002), Appl. Phys. Lett. 79,156 (2001), US Patent No. 7964293, US Patent Application Publication No. 2009/030202, International Publication No. 2004/080975, International Publication No. 2004/063159, International Publication No. 2005/085387, International Publication No. Public Publication No. 2006/067931, International Publication No. 2007/086552, International Publication No. 2008/114690, International Publication No. 2009/066942, International Publication No. 2009/066779, International Publication No. 2009/054253, International Publication No. 2011/086935, International Publication No. 2010/150593, International Publication No. 2010/047707, EP23111826, JP2010-251675A, JP2009-209133A, JP2009-124114A, JP 2 JP 08-277810 A, JP 2006-156445 A, JP 2005-340122 A, JP 2003-45662 A, JP 2003-31367 A, JP 2003-282270 A, International Publication 2012. / 115034.

  More preferable known electron transport materials in the present invention include aromatic heterocyclic compounds containing at least one nitrogen atom and compounds containing a phosphorus atom. For example, pyridine derivatives, pyrimidine derivatives, pyrazine derivatives, triazine derivatives, dibenzofurans. Derivatives, dibenzothiophene derivatives, azadibenzofuran derivatives, azadibenzothiophene derivatives, carbazole derivatives, azacarbazole derivatives, benzimidazole derivatives, arylphosphine oxide derivatives, and the like.

  The electron transport material may be used alone or in combination of two or more.

(Hole blocking layer)
The hole blocking layer is a layer having a function of an electron transport layer in a broad sense, and is preferably made of a material having a function of transporting electrons while having a small ability to transport holes, and transporting electrons while transporting holes. The probability of recombination of electrons and holes can be improved by blocking.

  Moreover, the structure of the electron carrying layer mentioned above can be used as a hole-blocking layer concerning this invention as needed.

  The hole blocking layer provided in the organic EL device of the present invention is preferably provided adjacent to the cathode side of the light emitting layer.

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

  As the material used for the hole blocking layer, the material used for the above-described electron transport layer is preferably used, and the material used as the above-described host compound is also preferably used for the hole blocking layer.

(Electron injection layer)
The electron injection layer (also referred to as “cathode buffer layer”) according to the present invention is a layer provided between the cathode and the light emitting layer in order to lower the driving voltage and improve the light emission luminance. It is described in detail in Chapter 2 “Electrode Materials” (pages 123 to 166) of the second edition of “The Forefront of Industrialization” (issued by NTT Corporation on November 30, 1998).

  In the present invention, the electron injection layer may be provided as necessary, and may be present between the cathode and the light emitting layer or between the cathode and the electron transport layer as described above.

  The electron injection layer is preferably a very thin film, and the layer thickness is preferably in the range of 0.1 to 5 nm, although it depends on the material. Moreover, the nonuniform layer (film | membrane) in which a constituent material exists intermittently may be sufficient.

  The details of the electron injection layer are described in JP-A-6-325871, JP-A-9-17574, JP-A-10-74586, and the like. Specific examples of materials preferably used for the electron injection layer are as follows. , Metals typified by strontium and aluminum, alkali metal compounds typified by lithium fluoride, sodium fluoride, potassium fluoride, etc., alkaline earth metal compounds typified by magnesium fluoride, calcium fluoride, etc., oxidation Examples thereof include metal oxides typified by aluminum, metal complexes typified by 8-hydroxyquinolinate lithium (Liq), and the like. Further, the above-described electron transport material can also be used.

  Moreover, the material used for said electron injection layer may be used independently, and may be used in combination of multiple types.

(Hole transport layer)
In the present invention, the hole transport layer is made of a material having a function of transporting holes and may have a function of transmitting holes injected from the anode to the light emitting layer.

  Although there is no restriction | limiting in particular about the total layer thickness of the positive hole transport layer which concerns on this invention, Usually, it is the range of 5 nm-5 micrometers, More preferably, it is 2-500 nm, More preferably, it is 5-200 nm.

  As a material used for the hole transport layer (hereinafter referred to as a hole transport material), any material that has either a hole injection property or a transport property or an electron barrier property may be used. Any one can be selected and used.

  For example, porphyrin derivatives, phthalocyanine derivatives, oxazole derivatives, oxadiazole derivatives, triazole derivatives, imidazole derivatives, pyrazoline derivatives, pyrazolone derivatives, phenylenediamine derivatives, hydrazone derivatives, stilbene derivatives, polyarylalkane derivatives, triarylamine derivatives, carbazole derivatives , Indolocarbazole derivatives, isoindole derivatives, acene derivatives such as anthracene and naphthalene, fluorene derivatives, fluorenone derivatives, and polyvinyl carbazole, polymer materials or oligomers with aromatic amines introduced into the main chain or side chain, polysilane, conductive And polymer (for example, PEDOT / PSS, aniline copolymer, polyaniline, polythiophene, etc.).

  Examples of the triarylamine derivatives include benzidine type typified by α-NPD (4,4′-bis [N- (1-naphthyl) -N-phenylamino] biphenyl), starburst type typified by MTDATA, Examples include compounds having fluorene or anthracene in the triarylamine-linked core.

  In addition, hexaazatriphenylene derivatives such as those described in JP-A-2003-519432 and JP-A-2006-135145 can also be used as a hole transport material.

  Furthermore, a hole transport layer having a high p property doped with impurities can also be used. Examples thereof include JP-A-4-297076, JP-A-2000-196140, 2001-102175, J. Pat. Appl. Phys. 95, 5773 (2004), and the like.

  JP-A-11-251067, J. Org. Huang et. al. It is also possible to use so-called p-type hole transport materials and inorganic compounds such as p-type-Si and p-type-SiC, as described in the literature (Applied Physics Letters 80 (2002), p. 139). Further, ortho-metalated organometallic complexes having Ir or Pt as the central metal represented by Ir (ppy) 3 are also preferably used.

  Although the above-mentioned materials can be used as the hole transport material, a triarylamine derivative, a carbazole derivative, an indolocarbazole derivative, an azatriphenylene derivative, an organometallic complex, or an aromatic amine is introduced into the main chain or side chain. The polymer materials or oligomers used are preferably used.

  Specific examples of known preferred hole transport materials used in the organic EL device of the present invention include the compounds described in the following documents in addition to the documents listed above, but the present invention is not limited thereto. Not.

  For example, Appl. Phys. Lett. 69, 2160 (1996), J. MoI. Lumin. 72-74,985 (1997), Appl. Phys. Lett. 78, 673 (2001), Appl. Phys. Lett. 90, 183503 (2007), Appl. Phys. Lett. 90, 183503 (2007), Appl. Phys. Lett. 51, 913 (1987), Synth. Met. 87, 171 (1997), Synth. Met. 91, 209 (1997), Synth. Met. 111, 421 (2000), SID Symposium Digest, 37, 923 (2006), J. Am. Mater. Chem. 3,319 (1993), Adv. Mater. 6, 677 (1994), Chem. Mater. 15, 3148 (2003), U.S. Patent Application Publication No. 2003/0162053, U.S. Patent Application Publication No. 2002/0158242, U.S. Patent Application Publication No. 2006/0240279, U.S. Patent Application Publication No. 2008/2008. No. 0220265, U.S. Patent No. 5061569, International Publication No. 2007/002683, International Publication No. 2009/018009, EP650955, U.S. Patent Application Publication No. 2008/0124572, U.S. Patent Publication No. 2007/0278938. Specification, US Patent Application Publication No. 2008/0106190, US Patent Application Publication No. 2008/0018221, International Publication No. 2012/115034, Japanese Translation of PCT International Publication No. 2003-519432, Japanese Patent Application Laid-Open No. 2006-135145 , It is a country patent application number 13/585981 issue like.

  The hole transport material may be used alone or in combination of two or more.

(Electron blocking layer)
The electron blocking layer is a layer having a function of a hole transport layer in a broad sense, and is preferably made of a material having a function of transporting holes and a small ability to transport electrons, while transporting holes. By blocking electrons, the probability of recombination of electrons and holes can be improved.

  Moreover, the structure of the positive hole transport layer mentioned above can be used as an electron blocking layer according to the present invention, if necessary.

  The electron blocking layer provided in the organic EL device of the present invention is preferably provided adjacent to the anode side of the light emitting layer.

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

  As the material used for the electron blocking layer, the material used for the above-described hole transport layer is preferably used, and the above-mentioned host compound is also preferably used for the electron blocking layer.

(Hole injection layer)
The hole injection layer (also referred to as “anode buffer layer”) according to the present invention is a layer provided between the anode and the light emitting layer for the purpose of lowering the driving voltage and improving the light emission luminance. It is described in detail in Chapter 2 “Electrode Materials” (pages 123 to 166) of the second edition of “The Forefront of Industrialization” (issued by NTT Corporation on November 30, 1998).

  In the present invention, the hole injection layer may be provided as necessary, and may be present between the anode and the light emitting layer or between the anode and the hole transport layer as described above.

  The details of the hole injection layer are also described in JP-A-9-45479, JP-A-9-260062, JP-A-8-288069, etc. Examples of the material used for the hole injection layer include: Examples thereof include materials used for the above-described hole transport layer.

  Among them, phthalocyanine derivatives typified by copper phthalocyanine, hexaazatriphenylene derivatives as described in JP-T-2003-519432 and JP-A-2006-135145, metal oxides typified by vanadium oxide, amorphous carbon Preferred are conductive polymers such as polyaniline (emeraldine) and polythiophene, orthometalated complexes represented by tris (2-phenylpyridine) iridium complex, and triarylamine derivatives.

  The materials used for the hole injection layer described above may be used alone or in combination of two or more.

(Additive)
The organic layer in the present invention described above may further contain other additives.
Examples of the additive include halogen elements such as bromine, iodine and chlorine, halogenated compounds, alkali metals and alkaline earth metals such as Pd, Ca, and Na, transition metal compounds, complexes, and salts.

  The content of the additive can be arbitrarily determined, but is preferably 1000 ppm or less, more preferably 500 ppm or less, and further preferably 50 ppm or less with respect to the total mass% of the contained layer. .

  However, it is not within this range depending on the purpose of improving the transportability of electrons and holes or the purpose of favoring the exciton energy transfer.

(Formation method of organic layer)
A method for forming an organic layer (hole injection layer, hole transport layer, light emitting layer, hole blocking layer, electron transport layer, electron injection layer, intermediate layer, etc.) according to the present invention will be described.

  The method for forming the organic layer according to the present invention is not particularly limited, and a conventionally known method such as a vacuum deposition method or a wet method (also referred to as a wet process) can be used.

  Examples of the wet method include spin coating, casting, ink jet, printing, die coating, blade coating, roll coating, spray coating, curtain coating, and LB (Langmuir-Blodgett). From the viewpoint of obtaining a homogeneous thin film easily and high productivity, a method with high roll-to-roll method suitability such as a die coating method, a roll coating method, an ink jet method and a spray coating method is preferable.

  Examples of the liquid medium for dissolving or dispersing the organic EL material used in the present invention include ketones such as methyl ethyl ketone and cyclohexanone, fatty acid esters such as ethyl acetate, halogenated hydrocarbons such as dichlorobenzene, toluene, xylene, Aromatic hydrocarbons such as mesitylene and cyclohexylbenzene, aliphatic hydrocarbons such as cyclohexane, decalin, and dodecane, and organic solvents such as DMF and DMSO can be used.

  Moreover, as a dispersion method, it can disperse | distribute by dispersion methods, such as an ultrasonic wave, high shear force dispersion | distribution, and media dispersion | distribution.

Further, different film forming methods may be applied for each layer. When a vapor deposition method is employed 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 to It is desirable to select appropriately within the range of 50 nm / second, substrate temperature −50 to 300 ° C., layer (film) thickness 0.1 nm to 5 μm, preferably 5 to 200 nm.

  The organic layer according to the present invention is preferably formed from the hole injection layer to the cathode consistently by a single evacuation, but it may be taken out halfway and subjected to different film formation methods. In that case, it is preferable to perform the work in a dry inert gas atmosphere.

(anode)
As the anode in the organic EL element, a material having a work function (4 eV or more, preferably 4.5 eV or more) of a metal, an alloy, an electrically conductive compound, or a mixture thereof is preferably used. Specific examples of such an electrode substance include a conductive transparent material such as a metal such as Au, CuI, indium tin oxide (ITO), SnO ₂ , and ZnO. Alternatively, an amorphous material such as IDIXO (In ₂ O ₃ —ZnO) capable of forming a transparent conductive film may be used.

  The anode may be formed by depositing a thin film of these electrode materials by vapor deposition or sputtering, and a pattern having a desired shape may be formed by photolithography, or when pattern accuracy is not so high (about 100 μm or more) A pattern may be formed through a mask having a desired shape at the time of vapor deposition or sputtering of the electrode material.

  Or when using the substance which can be apply | coated like an organic electroconductivity compound, wet film-forming methods, such as a printing system and a coating system, can also be used. When light emission is extracted from the anode, it is desirable that the transmittance be greater than 10%, and the sheet resistance as the anode is preferably several hundred Ω / □ or less.

  The film thickness of the anode depends on the material, but is usually selected within the range of 10 nm to 1 μm, preferably 10 to 200 nm.

(cathode)
As the cathode, a material 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 as an electrode material is used. Specific examples of such electrode materials include sodium, sodium-potassium alloy, magnesium, lithium, magnesium / copper mixture, magnesium / silver mixture, magnesium / aluminum mixture, magnesium / indium mixture, aluminum / aluminum oxide (Al ₂ O ₃ ) Mixtures, indium, lithium / aluminum mixtures, aluminum, rare earth metals and the like. Among these, from the point of durability against electron injection and oxidation, etc., a mixture of an electron injecting metal and a second metal which is a stable metal having a larger work function than this, for example, a magnesium / silver mixture, Magnesium / aluminum mixtures, magnesium / indium mixtures, aluminum / aluminum oxide (Al ₂ O ₃ ) mixtures, lithium / aluminum mixtures, aluminum and the like are preferred.

  The cathode can be produced by forming a thin film of these electrode materials by a method such as vapor deposition or sputtering. The sheet resistance as the cathode is preferably several hundred Ω / □ or less, and the film thickness is usually selected in the range of 10 nm to 5 μm, preferably 50 to 200 nm.

  In order to transmit the emitted light, if either one of the anode or the cathode of the organic EL element is transparent or translucent, the emission luminance is advantageously improved.

  Moreover, after producing the above metal with a film thickness of 1 to 20 nm on the cathode, a transparent or translucent cathode can be produced by producing a conductive transparent material mentioned in the description of the anode on the cathode. By applying the above, it is possible to manufacture a device in which both the anode and the cathode are transparent.

[Support substrate]
The support substrate (hereinafter also referred to as a substrate or a substrate) that can be used in the organic EL device of the present invention is not particularly limited in the type of glass, plastic and the like, and is transparent or opaque. May be. When extracting light from the support substrate side, the support substrate is preferably transparent. Examples of the transparent support substrate preferably used include glass, quartz, and a transparent resin film. A particularly preferable support substrate is a resin film capable of giving flexibility to the organic EL element.

  Examples of the resin film include polyesters such as polyethylene terephthalate (PET) and polyethylene naphthalate (PEN), polyethylene, polypropylene, cellophane, cellulose diacetate, cellulose triacetate (TAC), cellulose acetate butyrate, cellulose acetate propionate ( CAP), cellulose esters such as cellulose acetate phthalate, cellulose nitrate or derivatives thereof, polyvinylidene chloride, polyvinyl alcohol, polyethylene vinyl alcohol, syndiotactic polystyrene, polycarbonate, norbornene resin, polymethylpentene, polyether ketone, polyimide , Polyethersulfone (PES), polyphenylene sulfide, polysulfones, Cycloolefin resins such as polyetherimide, polyetherketoneimide, polyamide, fluororesin, nylon, polymethylmethacrylate, acrylic or polyarylate, Arton (trade name, manufactured by JSR) or Appel (trade name, manufactured by Mitsui Chemicals) Can be mentioned.

An inorganic film, an organic film, or a hybrid film of both may be formed on the surface of the resin film, and the water vapor permeability (25 ± 0.5 ° C.) measured by a method according to JIS K 7129-1992. , Relative humidity (90 ± 2)% RH) is preferably 0.01 g / m ² · 24 h or less of a barrier film, and further, oxygen permeability measured by a method according to JIS K 7126-1987. However, it is preferable that the film has a high barrier property of 1 × 10 ⁻³ ml / m ² · 24 h · atm or less and a water vapor permeability of 1 × 10 ⁻⁵ g / m ² · 24 h or less.

  As a material for forming the barrier film, any material may be used as long as it has a function of suppressing intrusion of elements that cause deterioration of elements such as moisture and oxygen. For example, silicon oxide, silicon dioxide, silicon nitride, or the like can be used. Further, in order to improve the brittleness of the film, it is more preferable to have a laminated structure of these inorganic layers and organic material layers. Although there is no restriction | limiting in particular about the lamination | stacking order of an inorganic layer and an organic layer, It is preferable to laminate | stack both alternately several times.

  The method for forming the barrier film is not particularly limited. For example, vacuum deposition, sputtering, reactive sputtering, molecular beam epitaxy, cluster ion beam, ion plating, plasma polymerization, atmospheric pressure plasma polymerization A plasma CVD method, a laser CVD method, a thermal CVD method, a coating method, or the like can be used, but an atmospheric pressure plasma polymerization method as described in JP-A-2004-68143 is particularly preferable.

  Examples of the opaque support substrate include metal plates such as aluminum and stainless steel, films, opaque resin substrates, and ceramic substrates.

  The external extraction quantum efficiency at room temperature (25 ° C.) of light emission of the organic EL device of the present invention is preferably 1% or more, and more preferably 5% or more.

  Here, external extraction quantum efficiency (%) = number of photons emitted to the outside of the organic EL element / number of electrons flowed to the organic EL element × 100.

  In addition, a hue improvement filter such as a color filter may be used in combination, or a color conversion filter that converts the emission color from the organic EL element into multiple colors using a phosphor may be used in combination.

[Sealing]
Examples of the sealing means used for sealing the organic EL element of the present invention include a method of bonding a sealing member, an electrode, and a support substrate with an adhesive. As a sealing member, it should just be arrange | positioned so that the display area | region of an organic EL element may be covered, and it may be concave plate shape or flat plate shape. Moreover, transparency and electrical insulation are not particularly limited.

  Specific examples include a glass plate, a polymer plate / film, and a metal plate / film. Examples of the glass plate include soda-lime glass, barium / strontium-containing glass, lead glass, aluminosilicate glass, borosilicate glass, barium borosilicate glass, and quartz. Examples of the polymer plate include polycarbonate, acrylic, polyethylene terephthalate, polyether sulfide, and polysulfone. Examples of the metal plate include those made of one or more metals or alloys selected from the group consisting of stainless steel, iron, copper, aluminum, magnesium, nickel, zinc, chromium, titanium, molybdenum, silicon, germanium, and tantalum.

In the present invention, a polymer film and a metal film can be preferably used because the organic EL element can be thinned. Furthermore, the polymer film has an oxygen permeability measured by a method according to JIS K 7126-1987 of 1 × 10 ⁻³ ml / m ² · 24 h or less, and measured by a method according to JIS K 7129-1992. The water vapor permeability (25 ± 0.5 ° C., relative humidity 90 ± 2%) is preferably 1 × 10 ⁻³ g / m ² · 24 h or less.

  For processing the sealing member into a concave shape, sandblasting, chemical etching, or the like is used.

  Specific examples of the adhesive include photocuring and thermosetting adhesives having reactive vinyl groups such as acrylic acid oligomers and methacrylic acid oligomers, and moisture curing adhesives such as 2-cyanoacrylates. be able to. Moreover, heat | fever and chemical curing types (two-component mixing), such as an epoxy type, can be mentioned. Moreover, hot-melt type polyamide, polyester, and polyolefin can be mentioned. Moreover, a cationic curing type ultraviolet curing epoxy resin adhesive can be mentioned.

  In addition, since an organic EL element may deteriorate by heat processing, what can be adhesive-hardened from room temperature to 80 degreeC is preferable. A desiccant may be dispersed in the adhesive. Application | coating of the adhesive agent to a sealing part may use commercially available dispenser, and may print like screen printing.

  In addition, it is also preferable that the electrode and the organic layer are coated on the outside of the electrode facing the support substrate with the organic layer interposed therebetween, and an inorganic or organic layer is formed in contact with the support substrate to form a sealing film. . In this case, the material for forming the film may be any material that has a function of suppressing intrusion of elements that cause deterioration of elements such as moisture and oxygen. For example, silicon oxide, silicon dioxide, silicon nitride, or the like may be used. it can.

  Further, in order to improve the brittleness of the film, it is preferable to have a laminated structure of these inorganic layers and layers made of organic materials. There are no particular limitations on the method of forming these films. For example, vacuum deposition, sputtering, reactive sputtering, molecular beam epitaxy, cluster ion beam, ion plating, plasma polymerization, atmospheric pressure plasma A combination method, a plasma CVD method, a laser CVD method, a thermal CVD method, a coating method, or the like can be used.

  In the gap between the sealing member and the display area of the organic EL element, an inert gas such as nitrogen or argon, or an inert liquid such as fluorinated hydrocarbon or silicon oil can be injected in the gas phase and liquid phase. preferable. A vacuum can also be used. Moreover, a hygroscopic compound can also be enclosed inside.

  Examples of the hygroscopic compound include metal oxides (for example, sodium oxide, potassium oxide, calcium oxide, barium oxide, magnesium oxide, aluminum oxide) and sulfates (for example, sodium sulfate, calcium sulfate, magnesium sulfate, cobalt sulfate). Etc.), metal halides (eg calcium chloride, magnesium chloride, cesium fluoride, tantalum fluoride, cerium bromide, magnesium bromide, barium iodide, magnesium iodide etc.), perchloric acids (eg perchloric acid) Barium, magnesium perchlorate, and the like), and anhydrous salts are preferably used in sulfates, metal halides, and perchloric acids.

[Protective film, protective plate]
In order to increase the mechanical strength of the element, a protective film or a protective plate may be provided outside the sealing film or the sealing film on the side facing the support substrate with the organic layer interposed therebetween. In particular, when sealing is performed by the sealing film, the mechanical strength is not necessarily high, and thus it is preferable to provide such a protective film and a protective plate. As a material that can be used for this, the same glass plate, polymer plate / film, metal plate / film, etc. used for the sealing can be used, but the polymer film is light and thin. Is preferably used.

[Light extraction improvement technology]
The organic EL element emits light inside a layer having a refractive index higher than that of air (within a refractive index of about 1.6 to 2.1), and is about 15% to 20% of light generated in the light emitting layer. It is generally said that it can only be taken out. This is because light incident on the interface (interface between the transparent substrate and air) at an angle θ greater than the critical angle causes total reflection and cannot be taken out of the device, This is because light is totally reflected between the light and the light is guided through the transparent electrode or the light emitting layer, and as a result, the light escapes in the direction of the side surface of the device.

  As a technique for improving the light extraction efficiency, for example, a method of forming irregularities on the surface of the transparent substrate to prevent total reflection at the transparent substrate and the air interface (for example, US Pat. No. 4,774,435), A method for improving efficiency by providing light condensing property (for example, JP-A-63-314795), a method for forming a reflective surface on a side surface of an element (for example, JP-A-1-220394), a substrate, etc. A method of forming an antireflection film by introducing a flat layer having an intermediate refractive index between the substrate and the light emitter (for example, Japanese Patent Application Laid-Open No. 62-172691), lower refraction than the substrate between the substrate and the light emitter A method of introducing a flat layer having a refractive index (for example, Japanese Patent Application Laid-Open No. 2001-202827), and a method of forming a diffraction grating between any one of the substrate, the transparent electrode layer and the light emitting layer (including between the substrate and the outside) JP-A-11 No. 283,751 Publication), and the like.

  In the present invention, these methods can be used in combination with the organic EL device of the present invention. However, a method of introducing a flat layer having a lower refractive index than the substrate between the substrate and the light emitter, or a substrate, transparent A method of forming a diffraction grating between any layers of the electrode layer and the light emitting layer (including between the substrate and the outside) can be suitably used.

  In the present invention, by combining these means, it is possible to obtain an element having higher luminance or durability.

  When a low refractive index medium is formed between the transparent electrode and the transparent substrate with a thickness longer than the wavelength of light, the light extracted from the transparent electrode has a higher extraction efficiency to the outside as the refractive index of the medium is lower. Become.

  Examples of the low refractive index layer include aerogel, porous silica, magnesium fluoride, and a fluorine-based polymer. Since the refractive index of the transparent substrate is generally in the range of about 1.5 to 1.7, the low refractive index layer preferably has a refractive index of about 1.5 or less. Furthermore, it is preferable that it is 1.35 or less.

  The thickness of the low refractive index medium is preferably at least twice the wavelength in the medium. This is because the effect of the low refractive index layer is diminished when the thickness of the low refractive index medium is about the wavelength of light and the electromagnetic wave exuded by evanescent enters the substrate.

  The method of introducing a diffraction grating into an interface that causes total reflection or in any medium has a feature that the effect of improving the light extraction efficiency is high. This method uses the property that the diffraction grating can change the direction of light to a specific direction different from refraction by so-called Bragg diffraction, such as first-order diffraction or second-order diffraction. The light that cannot be emitted due to total internal reflection between layers is diffracted by introducing a diffraction grating into any layer or medium (in the transparent substrate or transparent electrode). , Trying to extract light out.

  The introduced diffraction grating desirably has a two-dimensional periodic refractive index. This is because light emitted from the light-emitting layer is randomly generated in all directions, so a general one-dimensional diffraction grating having a periodic refractive index distribution only in a certain direction diffracts only light traveling in a specific direction. The light extraction efficiency does not increase so much.

  However, by making the refractive index distribution a two-dimensional distribution, light traveling in all directions is diffracted, and light extraction efficiency is increased.

  The position where the diffraction grating is introduced may be in any of the layers or in the medium (in the transparent substrate or the transparent electrode), but is preferably in the vicinity of the organic light emitting layer where light is generated. At this time, the period of the diffraction grating is preferably within a range of about 1/2 to 3 times the wavelength of light in the medium. The arrangement of the diffraction gratings is preferably two-dimensionally repeated, such as a square lattice, a triangular lattice, or a honeycomb lattice.

[Condensing sheet]
The organic EL element of the present invention is fronted with respect to a specific direction, for example, the element light emitting surface, by combining a so-called condensing sheet, for example, by providing a structure on the microlens array on the light extraction side of the support substrate (substrate). By condensing in the direction, the luminance in a specific direction can be increased.

  As an example of the microlens array, quadrangular pyramids having a side of 30 μm and an apex angle of 90 degrees are arranged two-dimensionally on the light extraction side of the substrate. One side is preferably within a range of 10 to 100 μm. If it becomes smaller than this, the effect of diffraction will generate | occur | produce and color, and if too large, thickness will become thick and is not preferable.

  As the condensing sheet, for example, a sheet that is put into practical use in an LED backlight of a liquid crystal display device can be used. As such a sheet, for example, a brightness enhancement film (BEF) manufactured by Sumitomo 3M Limited can be used. As the shape of the prism sheet, for example, the base material may be formed by forming a △ -shaped stripe having a vertex angle of 90 degrees and a pitch of 50 μm, or the vertex angle is rounded and the pitch is changed randomly. Other shapes may be used.

  Moreover, in order to control the light emission angle from an organic EL element, you may use a light-diffusion plate and a film together with a condensing sheet. For example, a diffusion film (light-up) manufactured by Kimoto Co., Ltd. can be used.

[Usage]
The organic EL element of the present invention can be used as an electronic device such as a display device, a display, and various light emitting devices.

  Examples of light emitting devices include lighting devices (home lighting, interior lighting), clocks and backlights for liquid crystals, billboard advertisements, traffic lights, light sources of optical storage media, light sources of electrophotographic copying machines, light sources of optical communication processors, light Although the light source of a sensor etc. are mentioned, It is not limited to this, Especially, it can use effectively for the use as a backlight of a liquid crystal display device, and a light source for illumination.

  In the organic EL element of the present invention, patterning may be performed by a metal mask, an ink jet printing method, or the like as needed during film formation. In the case of patterning, only the electrode may be patterned, the electrode and the light emitting layer may be patterned, or the entire layer of the element may be patterned. In the fabrication of the element, a conventionally known method is used. Can do.

4). Display Device The display device including the organic EL element of the present invention may be either 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 vapor deposition, casting, spin coating, ink jet, printing, or the like.

  In the case of patterning only the light emitting layer, there is no limitation on the method, but a vapor deposition method, an inkjet method, a spin coating method, and a printing method are preferable.

  The configuration of the organic EL element provided in the display device is selected from the above-described configuration examples of the organic EL element as necessary.

  Moreover, the manufacturing method of an organic EL element is as having shown to the one aspect | mode of manufacture of the organic EL element of said invention.

  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, or 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 or display include a television, a personal computer, a mobile device, an AV device, a character broadcast display, and an information display in an automobile. 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 devices include household lighting, interior lighting, clock and liquid crystal backlights, billboard advertisements, traffic lights, optical storage media light sources, electrophotographic copying machine light sources, optical communication processor light sources, optical sensor light sources, etc. However, the present invention is not limited to these.

  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. 5 is a schematic view showing an example of a display device composed of 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, a wiring unit C that electrically connects the display unit A and the control unit B, and the like.

  The control unit B is electrically connected to the display unit A via the wiring unit C, and sends a scanning signal and an image data signal to each of a plurality of pixels based on image information from the outside. Sequentially emit light according to the image data signal, scan the image, and display the image information on the display unit A.

  FIG. 6 is a schematic diagram of a display device using an active matrix method.

  The display unit A includes a wiring unit C 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.

  FIG. 6 shows a case where the light emitted from the pixel 3 is extracted in the direction of the white arrow (downward).

  The scanning line 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 grid pattern and are connected to the pixels 3 at the orthogonal positions (details are illustrated). Not)

  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 on the same substrate.

  Next, the light emission process of the pixel will be described. FIG. 7 is a schematic diagram showing a pixel circuit.

  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. 7, 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, since the capacitor 13 holds the charged potential of the image data signal even if the driving of the switching transistor 11 is turned off, 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 by turning on / off a predetermined light emission amount by a binary image data signal. Good. 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. 8 is a schematic view of a passive matrix display device. In FIG. 8, 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.

  By using the organic EL element of the present invention, a display device with improved luminous efficiency was obtained.

5. Lighting Device The organic EL element of the present invention can also be used for a lighting device.
The organic EL element of the present invention may be used as an organic EL element having a resonator structure. Examples of the purpose of use of the organic EL element having such a resonator structure include a light source of an optical storage medium, a light source of an electrophotographic copying machine, a light source of an optical communication processing machine, and a light source of an optical sensor. It is not limited. 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).

  The driving method when used as a display device for reproducing a moving image may be either a passive matrix method or an active matrix method. Alternatively, it is possible to produce a full-color display device by using two or more organic EL elements of the present invention having different emission colors.

  In addition, the π-conjugated compound used in the present invention can be applied to a lighting device including an organic EL element that emits substantially white light. For example, when a plurality of light emitting materials are used, white light emission can be obtained by simultaneously emitting a plurality of light emission colors and mixing the colors. The combination of a plurality of emission colors may include three emission maximum wavelengths of three primary colors of red, green, and blue, or two of the 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, the organic EL device forming method of the present invention may be simply arranged by providing a mask only when forming a light emitting layer, a hole transport layer, an electron transport layer, or the like, and separately coating with the mask. Since the other layers are common, patterning of a mask or the like is unnecessary, and for example, an electrode film can be formed on one surface by a vapor deposition method, a cast method, a spin coating method, an ink jet method, a printing method, or the like, and productivity is 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 emit white light.

[One Embodiment of Lighting Device of the Present Invention]
One aspect of the lighting device of the present invention that includes the organic EL element of the present invention will be described.

  The non-light emitting surface of the organic EL device of the present invention is covered with a glass case, a 300 μm thick glass substrate is used as a sealing substrate, and an epoxy photocurable adhesive (LUX The track LC0629B) is applied, and this is overlaid on the cathode and brought into close contact with the transparent support substrate, irradiated with UV light from the glass substrate side, cured, sealed, and illuminated as shown in FIG. 9 and FIG. A device can be formed.

  FIG. 9 shows a schematic diagram of a lighting device, and the organic EL element (organic EL element 101 in the lighting device) of the present invention is covered with a glass cover 102 (note that the sealing operation with the glass cover is performed by lighting. This was performed in a glove box under a nitrogen atmosphere (in an atmosphere of high-purity nitrogen gas having a purity of 99.999% or more) without bringing the organic EL element 101 in the apparatus into contact with the air.

  FIG. 10 is a cross-sectional view of the lighting device, 105 is a cathode, 106 is an organic layer, and 107 is a glass substrate with a transparent electrode. The glass cover 102 is filled with nitrogen gas 108 and a water catching agent 109 is provided.

  By using the organic EL element of the present invention, a lighting device with improved luminous efficiency can be obtained.

6). Light-Emitting Thin Film The light-emitting thin film according to the present invention contains the above-described π-conjugated compound according to the present invention, and can be produced in the same manner as the method for forming the organic layer.

  The light-emitting thin film of the present invention can be produced in the same manner as the method for forming the organic layer.

  The method for forming the light-emitting thin film of the present invention is not particularly limited, and a conventionally known method such as a vacuum deposition method or a wet method (also referred to as a wet process) can be used.

  Examples of the wet method include spin coating, casting, ink jet, printing, die coating, blade coating, roll coating, spray coating, curtain coating, and LB (Langmuir-Blodgett). From the viewpoint of obtaining a homogeneous thin film easily and high productivity, a method with high roll-to-roll method suitability such as a die coating method, a roll coating method, an ink jet method and a spray coating method is preferable.

  Examples of the liquid medium for dissolving or dispersing the light emitting material used in the present invention include ketones such as methyl ethyl ketone and cyclohexanone, fatty acid esters such as ethyl acetate, halogenated hydrocarbons such as dichlorobenzene, toluene, xylene, and mesitylene. Aromatic hydrocarbons such as cyclohexylbenzene, aliphatic hydrocarbons such as cyclohexane, decalin, and dodecane, and organic solvents such as DMF and DMSO can be used.

  Moreover, as a dispersion method, it can disperse | distribute by dispersion methods, such as an ultrasonic wave, high shear force dispersion | distribution, and media dispersion | distribution.

Further, different film forming methods may be applied for each layer. When a vapor deposition method is employed for film formation, the vapor deposition conditions vary depending on the type of compound used, but generally the boat heating temperature is in the range of 50 to 450 ° C., and the degree of vacuum is in the range of 10 ⁻⁶ to 10 ⁻² Pa. Of these, the deposition rate is appropriately selected within the range of 0.01 to 50 nm / second, the substrate temperature within the range of −50 to 300 ° C., the layer thickness within the range of 0.1 nm to 5 μm, and preferably within the range of 5 to 200 nm. desirable.

  When a spin coat method is employed for film formation, it is preferable to perform the spin coater within a range of 100 to 1000 rpm and within a range of 10 to 120 seconds in a dry inert gas atmosphere.

  EXAMPLES Hereinafter, the present invention will be specifically described with reference to examples, but the present invention is not limited thereto. In addition, although the display of "%" is used in an Example, unless otherwise indicated, "mass%" is represented.

List of compounds used in this example.

1. Synthesis of π-conjugated compound (Compound T-19)
Compound T-19 was synthesized in the same manner as described in WO2010 / 113755. Specifically, compound T-19 was obtained by reacting indoloindole with 2,5-dichloropyrazine under basic conditions in the same manner as described in International Publication No. 2010/113755. .

  In the same manner as described above, compounds T-2, T-9, T-15, T-21, T-22, T-23, T-25, T-32, T-36, T-43, T-44 , T-58 was synthesized.

The Delta] E _ST of the obtained compound, was calculated in the following manner.

(Calculation of ΔE _ST)
Structural optimization calculation was performed with molecular orbital calculation software using B3LYP as the functional and 6-31G (d) as the basis function. As molecular orbital calculation software, Gaussian 09 (Revision C.01, MJ Frisch, et al, Gaussian, Inc., 2010.) manufactured by Gaussian, USA was used. Furthermore, the excitation state calculation by the time-dependent density functional method (Time-Dependent DFT) was performed. Thereby, energy levels E (S1) and E (T1) of each compound were obtained. The resulting value, by applying the following formula to calculate the Delta] E _ST.
ΔE _ST = | E (S1) −E (T1) |

[Example 1]
(Preparation of organic EL element 1-1)
A transparent substrate with an ITO (Indium Tin Oxide) film having a thickness of 150 nm formed on a glass substrate of 50 mm × 50 mm and a thickness of 0.7 mm, patterned, and this ITO transparent electrode was attached After ultrasonic cleaning with isopropyl alcohol, drying with dry nitrogen gas and UV ozone cleaning for 5 minutes, this transparent substrate was fixed to a substrate holder of a commercially available vacuum deposition apparatus.
Each of the vapor deposition crucibles in the vacuum vapor deposition apparatus was filled with the constituent material of each layer in an amount optimal for device fabrication. The evaporation crucible used was made of a resistance heating material made of molybdenum or tungsten.

After depressurizing to a vacuum degree of 1 × 10 ⁻⁴ Pa, the deposition crucible containing HI-1 (1,4,5,8,9,12-hexaazatriphenylenehexacarbonitrile) was energized and heated to deposit Vapor deposition was performed on the ITO transparent electrode at a speed of 0.1 nm / second to form a hole injection transport layer having a layer thickness of 10 nm.

  Subsequently, α-NPD (4,4′-bis [N- (1-naphthyl) -N-phenylamino] biphenyl) was deposited on the hole injection layer at a deposition rate of 0.1 nm / second, and the layer thickness was 40 nm. The hole transport layer was formed. The host compound mCP (1,3-bis (N-carbazolyl) benzene) and the comparative compound 1 were co-deposited at a deposition rate of 0.1 nm / second so as to be 94% and 6% by volume, respectively, and the layer thickness was 30 nm. The light emitting layer was formed.

  Thereafter, BCP (2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline) was deposited at a deposition rate of 0.1 nm / second to form an electron transport layer having a layer thickness of 30 nm.

  Furthermore, after forming lithium fluoride with a film thickness of 0.5 nm, 100 nm of aluminum was vapor-deposited to form a cathode.

  The non-light-emitting surface side of the above element was covered with a can-shaped glass case in an atmosphere of high purity nitrogen gas having a purity of 99.999% or more, and an electrode lead-out wiring was installed to prepare an organic EL element 1-1.

(Preparation of organic EL elements 1-2 to 1-16)
Organic EL elements 1-2 to 1-16 were produced in the same manner as the organic EL element 1-1 except that the luminescent compound was changed from the comparative compound 1 as shown in Table 1.

(Measurement of relative luminous efficiency)
The obtained organic EL device was allowed to emit light at room temperature (about 25 ° C.) and a constant current of ^2.5 mA / cm ² . And the light emission luminance of the organic EL element immediately after the start of light emission was measured using a spectral radiance meter CS-2000 (manufactured by Konica Minolta).
The obtained light emission luminance was applied to the following formula, and the relative light emission luminance with respect to the light emission luminance of the organic EL element 1-1 was determined.
Relative light emission luminance (%) = (light emission luminance of each organic EL element / light emission luminance of organic EL element 1-1) × 100
The obtained measurement results are shown in Table 1.

The organic EL elements 1-4 to 1-16 containing the luminescent material of the present invention as the luminescent material exhibit higher emission luminance than the organic EL elements 1-1, 1-2, and 1-3 containing the comparative compound. I understand. Particularly Delta] E _ST the following compounds 0.50EV, compared with comparative compounds 3 Delta] E _ST exceeds 0.50EV, it can be seen that a high luminous efficiency.

[Example 2]
(Preparation of organic EL element 2-1)
Transparent support provided with this ITO transparent electrode after patterning on a substrate (NH45 manufactured by NH Techno Glass Co., Ltd.) formed by depositing 100 nm of ITO (indium tin oxide) on a glass substrate of 100 mm × 100 mm × 1.1 mm as an anode The substrate was ultrasonically cleaned with isopropyl alcohol, dried with dry nitrogen gas, and subjected to UV ozone cleaning for 5 minutes.

  On this transparent support substrate, using a solution obtained by diluting poly (3,4-ethylenedioxythiophene) -polystyrene sulfonate (PEDOT / PSS, Bayer, Baytron P Al 4083) to 70% with pure water, 3000 rpm, A thin film was formed by spin coating under conditions of 30 seconds, and then dried at 200 ° C. for 1 hour to provide a hole injection layer having a layer thickness of 20 nm. This transparent support substrate was fixed to a substrate holder of a commercially available vacuum vapor deposition apparatus, and each of the vapor deposition crucibles in the vacuum vapor deposition apparatus was filled with a constituent material of each layer in an amount optimal for device fabrication. The evaporation crucible used was made of a resistance heating material made of molybdenum or tungsten.

After reducing the pressure to 1 × 10 ⁻⁴ Pa, α-NPD was deposited on the hole injection layer at a deposition rate of 0.1 nm / second to form a hole transport layer having a layer thickness of 40 nm.
Next, CDBP as the host material and 2,5,8,11-tetra-t-butylperylene as the luminescent material were co-deposited at a deposition rate of 0.1 nm / second so as to be 97% and 3% by volume, respectively. Evaporation was performed to form a light emitting layer with a layer thickness of 30 nm.

Thereafter, TPBi (1,3,5-tris (N-phenylbenzimidazol-2-yl)) was deposited at a deposition rate of 0.1 nm / second to form an electron transport layer having a layer thickness of 30 nm.
Furthermore, after forming sodium fluoride with a film thickness of 1 nm, 100 nm of aluminum was vapor-deposited to form a cathode.
The non-light-emitting surface side of the above element was covered with a can-shaped glass case in an atmosphere of high purity nitrogen gas having a purity of 99.999% or more, and an electrode lead-out wiring was installed to prepare an organic EL element 2-1.

(Preparation of organic EL element 2-2)
Using CDBP as the host compound, 2,5,8,11-tetra-t-butylperylene as the luminescent compound, and comparative compound 1 as the third component, the respective ratios were 82%, 3%, and 15% by volume. An organic EL element 2-2 was produced in the same manner as the production of the organic EL element 2-1, except that the light emitting layer was formed.

(Production of organic EL elements 2-3 to 2-8)
As shown in Table 2, organic EL elements 2-3 to 2-8 were produced in the same manner as the organic EL element 2-2 except that the third component was changed.

  In the same manner as described above, the light emission luminance of the organic EL element 2-1 was measured, and the relative light emission luminance of each organic EL element with respect to the light emission luminance of the organic EL element 2-1 was obtained. The obtained measurement results are shown in Table 2.

Organic EL elements 2-5 to 2-8 containing the luminescent material of the present invention as the third component include organic EL elements 2-1 not containing the third component, and organic EL elements 2-2, 2 containing the comparative compound. It can be seen that the emission luminance is higher than -3 and 2-4. Particularly Delta] E _ST the following compounds 0.50EV, compared with comparative compounds 3 Delta] E _ST exceeds 0.50EV, it can be seen that a high luminous efficiency.

[Example 3]
(Preparation of organic EL element 3-1)
A transparent substrate with an ITO (Indium Tin Oxide) film formed at a thickness of 150 nm as a positive electrode on a glass substrate of 50 mm × 50 mm and a thickness of 0.7 mm, patterned, and then attached with this ITO transparent electrode After ultrasonic cleaning with isopropyl alcohol, drying with dry nitrogen gas and UV ozone cleaning for 5 minutes, this transparent substrate was fixed to a substrate holder of a commercially available vacuum deposition apparatus.

  Each of the resistance heating boats for vapor deposition in the vacuum vapor deposition apparatus was filled with the constituent material of each layer in an amount optimal for device fabrication. The resistance heating boat was made of molybdenum or tungsten.

After reducing the vacuum to 1 × 10 ⁻⁴ Pa, the resistance heating boat containing HI-1 was energized and heated, and deposited on the ITO transparent electrode at a deposition rate of 0.1 nm / second. A hole injection layer was formed.

  Next, α-NPD (4,4′-bis [N- (1-naphthyl) -N-phenylamino] biphenyl) is deposited at a deposition rate of 0.1 nm / second to form a hole transport layer having a layer thickness of 30 nm. did.

  Next, the resistance heating boat containing Comparative Compound 1 as a host material and GD-1 as a luminescent material was energized and heated, and the deposition rate was 0.1 nm / second and 0.010 nm / second on the hole transport layer, respectively. A light emitting layer having a layer thickness of 40 nm was formed by co-evaporation.

  Subsequently, HB-1 was deposited at a deposition rate of 0.1 nm / second to form a first electron transport layer having a layer thickness of 5 nm.

  Further thereon, ET-1 was deposited at a deposition rate of 0.1 nm / second to form a second electron transport layer having a layer thickness of 45 nm.

  Then, after vapor-depositing lithium fluoride so that it might become 0.5 nm in thickness, 100 nm of aluminum was vapor-deposited, the cathode was formed, and the organic EL element 3-1 was produced.

(Production of organic EL elements 3-2 to 3-9)
Organic EL elements 3-2 to 3-9 were produced in the same manner as the organic EL element 3-1, except that the host material was changed as shown in Table 3.

  In the same manner as described above, the light emission luminance of the organic EL element 3-1 was measured, and the relative light emission luminance of each organic EL element with respect to the light emission luminance of the organic EL element 3-1 was obtained. The obtained measurement results are shown in Table 3.

Organic EL elements 3-4 to 3-9 containing the light-emitting material of the present invention as a host material exhibit higher emission luminance than organic EL elements 3-1, 3-2 and 3-3 containing a comparative compound. I understand. Particularly Delta] E _ST the following compounds 0.50EV, compared with comparative compounds 3 Delta] E _ST exceeds 0.50EV, it can be seen that a high luminous efficiency.

  This application claims the priority based on Japanese Patent Application No. 2015-095806 of May 8, 2015 application. The contents described in the claims, specification, and drawings of the application are all incorporated herein by reference.

  ADVANTAGE OF THE INVENTION According to this invention, the luminescent material which can improve luminous efficiency can be provided, without lengthening luminescence wavelength.

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 101 Organic EL element in a lighting device 102 Glass cover 105 Cathode 106 Organic layer 107 Glass substrate 108 with transparent electrode 108 Nitrogen gas 109 Water trapping agent A Display part B Control part C Wiring part

Claims (13)

A π-conjugated compound having a structure represented by the following general formula (1).

(In general formula (1),
D ¹ and D ² are each independently selected from the group consisting of an aryl group substituted with an electron donating group, an optionally substituted electron donating heterocyclic group, and an optionally substituted amino group. Represents an electron donating group D
M ¹ ~M ⁴ each independently represents a nitrogen atom or ^-C-Z, at least one of M 1 ~M ⁴ is a nitrogen ^atom, or is -C of M 1 ~M ⁴ In the case of -Z, Z represents a hydrogen atom, a deuterium atom, or a substituent each independently. ) The substituent is the electron donating group D or an alkyl group, or a fluorine atom, a cyano group, an alkyl group substituted with a fluorine atom, an optionally substituted carbonyl group, or an optionally substituted sulfonyl. A group, an optionally substituted phosphine oxide group, an optionally substituted boryl group, an aryl group optionally substituted with an electron withdrawing group, and an optionally substituted electron withdrawing heterocyclic group The π-conjugated compound according to claim 1, which is an electron-withdrawing group A selected from the group consisting of The π-conjugated compound according to claim 1, represented by any one of the following general formulas (2) to (21).

(In the general formulas (2) to (21),
D ^{1 to} D ⁶ each independently represent the electron donating group D;
Z ^{1 to} Z ⁴ each independently represent a hydrogen atom, a deuterium atom, an alkyl group, or the electron-withdrawing group A. ) The π-conjugated compound according to claim 3, wherein in the general formulas (2) to (21), Z ^{1 to} Z ⁴ are an electron-withdrawing group A. In the [pi conjugated compound ^satisfies at least one of ^{D 1 = D 2 = D 3} = D 4 = D 5 = D 6 and ^{Z 1 = Z 2 = Z 3} = Z 4, according to claim 3 [pi Conjugated compounds. The π-conjugated compound according to claim 1, wherein an absolute value (ΔE _ST ) of an energy difference between the lowest excited singlet level and the lowest excited triplet level of the π-conjugated compound is 0.50 eV or less.   An organic electroluminescent device material comprising the π-conjugated compound according to claim 1.   A luminescent thin film comprising the π-conjugated compound according to claim 1. An anode, a cathode, and a light emitting layer provided between the anode and the cathode,
The organic electroluminescent element in which at least one layer of the light emitting layer contains the π-conjugated compound according to claim 1.   The organic electroluminescence device according to claim 9, wherein the light-emitting layer includes the π-conjugated compound and at least one of a fluorescent compound and a phosphorescent compound.   The organic electroluminescent element according to claim 9, wherein the light-emitting layer includes the π-conjugated compound, at least one of a fluorescent compound and a phosphorescent compound, and a host material.   A display device comprising the organic electroluminescence element according to claim 9.   The illuminating device which has an organic electroluminescent element of Claim 9.

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