JP2003123981A - Organic light emitting device - Google Patents

Abstract

(57) [Problem] To provide a red organic light-emitting device having extremely high efficiency, high luminance, and long life light output. SOLUTION: A pair of electrodes comprising an anode and a cathode,
In an organic light-emitting element having at least one layer containing one or more organic compounds sandwiched between the pair of electrodes, at least one of the layers containing the organic compounds contains thiadiazole represented by the following general formula [1] or various kinds thereof. An organic light-emitting device comprising at least one benzobisazomethine complex having a diazole ring fused thereto. Embedded image

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an organic light emitting device, and more particularly to a device that emits light by applying an electric field to a thin film containing an organic compound.

[0002]

2. Description of the Related Art In an organic light emitting device, a thin film containing a fluorescent organic compound is sandwiched between an anode and a cathode and electrons and holes are injected from each electrode to excite excitons of the fluorescent compound. It is an element that uses the light emitted when the excitons return to the ground state.

1987 Research by Kodak Company (Appl.
Phys. Lett. 51, 913 (1987)), an anode is made of ITO, a cathode is made of a magnesium-silver alloy, an aluminum quinolinol complex is used as an electron transporting material and a light emitting material, and a triphenylamine derivative is used as a hole transporting material. A two-layer device with an applied voltage of about 10 V is 1000 cd / m ²
Some light emission has been reported. Related patents include US Pat. No. 4,539,507 and US Pat. No. 4,720,4.
32, US Pat. No. 4,885,211 and the like.

Further, it is possible to emit light from ultraviolet to infrared by changing the kind of the fluorescent organic compound, and recently, various compounds have been actively researched. For example, US Pat. No. 5,151,629, US Pat.
9,783, US Pat. No. 5,382,477, JP-A-2-247278, JP-A-3-255190, JP-A-5-202356, JP-A-9-202.
No. 878, Japanese Patent Laid-Open No. 9-227576, and the like.

Further, in addition to the organic light emitting device using the low molecular weight material as described above, an organic light emitting device using a conjugated polymer is also available at the group of Cambridge University (Nature,
347, 539 (1990)).
In this report, light emission is confirmed in a single layer by depositing polyphenylene vinylene (PPV) in a coating system.
Related patents for organic light emitting devices using conjugated polymers include US Pat. No. 5,247,190 and US Pat.
4,878, US Pat. No. 5,672,678, JP-A-4-145192, JP-A-5-247460 and the like.

As described above, the recent progress in organic light-emitting devices is remarkable, and the features thereof are that it is possible to realize a light-emitting device with high luminance, diversity of emission wavelength, high-speed response, thinness and light weight at a low applied voltage. It suggests the possibility of a wide range of applications.

However, under the present circumstances, further higher brightness light output or higher conversion efficiency is required. Further, there are still many problems in terms of durability such as deterioration with time due to long-term use and deterioration due to atmospheric gas containing oxygen or moisture. Further, in consideration of application to a full-color display or the like, light emission of blue, green, and red with good color purity is required, but this problem has not been sufficiently solved yet.

A large number of compounds having a heterocycle have been studied as fluorescent organic compounds used in the electron transport layer and the light emitting layer. Examples thereof include a pyrrole compound, a thiophene compound, an oxazole compound, an oxadiazole compound, a thiadiazole compound, an imidazole compound, and a pyrazine compound. Regarding oxazole compounds, which have relatively many reports among them, for example, JP-A-5-214335 and JP-A-9-188876.
JP-A No. 5-345686 and JP-A No. 11-345686.
For example, Japanese Patent Application Laid-Open No. 2000-95766 discloses imidazole compounds.
Regarding the pyrazine compound, for example, US Pat.
No. 77142, JP-A-8-73443, etc. are mentioned, but sufficiently satisfactory emission brightness and durability,
No red organic light emitting device having an emission wavelength has been obtained.

[0009]

SUMMARY OF THE INVENTION The present invention has been made to solve the above problems of the prior art, and is a red organic light emitting device having an extremely high efficiency, high brightness, and long life light output. The purpose is to provide.

Another object of the present invention is to provide an organic light emitting device which is easy to manufacture and can be manufactured at a relatively low cost.

[0011]

Means for Solving the Problems As a result of intensive studies for solving the above problems, the present inventors have found that a pair of electrodes consisting of an anode and a cathode and one or a plurality of electrodes sandwiched between the pair of electrodes. In the organic light-emitting device having at least a layer containing an organic compound, at least one layer of the layers containing an organic compound contains a specific compound, thereby providing a red organic light-emitting device having a light output with higher efficiency and higher brightness. The inventors have found that it can be created, and have completed the present invention.

That is, the organic light-emitting device of the present invention is an organic light-emitting device having at least a pair of electrodes consisting of an anode and a cathode, and a layer containing one or a plurality of organic compounds sandwiched between the pair of electrodes. At least one of the layers containing an organic compound is characterized by containing at least one benzobisazomethine complex represented by the following general formula [1] in which a thiadiazole or various diazole rings are condensed.

[0013]

[Chemical 4]

(Wherein R ₁ and R ₂ are hydrogen atom, halogen atom, nitro group, nitrile group, substituted silyl group, substituted or unsubstituted alkyl group, substituted or unsubstituted alkenyl group, substituted or unsubstituted Aralkyl group, substituted or unsubstituted aryl group, substituted or unsubstituted amino group, substituted or unsubstituted azomethine group, substituted or unsubstituted carbonyl group, substituted or unsubstituted alkoxy group, substituted or unsubstituted ether A group selected from the group consisting of a group, a substituted or unsubstituted heterocyclic group, and Ar ₁ and Ar ₂ are groups selected from a substituted or unsubstituted aryl group and a substituted or unsubstituted heterocyclic group. There may .Y ₁ and Y ₂ be different even in the same is oxygen atom, a sulfur atom, the group consisting of substituted or unsubstituted amino group Ri is a group selected may .X ₁ be different even in the same, the sulfur atom, sulfoxide, sulfone, an oxygen atom, a group selected from the group consisting of selenium atom, be the same M ₁ is a typical element such as Be, Ca, Mg or Sn, B 1
a, Cd, Co, Cr, Cu, Fe, Ni, Pb, P
The transition metal elements such as d, Pt, Sr, Ti, V, and Zn are shown. )

Another organic light emitting device of the present invention is an organic light emitting device having at least a pair of electrodes consisting of an anode and a cathode and a layer containing one or a plurality of organic compounds sandwiched between the pair of electrodes. At least one layer of the organic compound-containing layer contains at least one benzobisazomethine complex having a thiadiazole or various diazole rings condensed by the following general formula [2].

[0016]

[Chemical 5]

(In the formula, R ₃ is a hydrogen atom, a halogen atom, a nitro group, a nitrile group, a substituted silyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aralkyl group. Substituted or unsubstituted aryl group, substituted or unsubstituted amino group, substituted or unsubstituted azomethine group, substituted or unsubstituted carbonyl group, substituted or unsubstituted alkoxy group, substituted or unsubstituted ether group, substituted Alternatively, it is a group selected from the group consisting of unsubstituted heterocyclic groups.
r ₃ and Ar ₄ are a substituted or unsubstituted aryl group,
A group selected from a substituted or unsubstituted heterocyclic group,
It may be the same or different. Y ₃ and Y ₄ are
It is a group selected from the group consisting of an oxygen atom, a sulfur atom and a substituted or unsubstituted amino group, and may be the same or different. X ₂ is a sulfur atom, sulfoxide,
It is a group selected from the group consisting of sulfone, oxygen atom and selenium atom, and may be the same or different. M ₂
Is a typical element such as Be, Ca, Mg, Sn, Ba, C
d, Co, Cr, Cu, Fe, Ni, Pb, Pd, P
The transition metal elements such as t, Sr, Ti, V, and Zn are shown. )

Still another organic light emitting device of the present invention is an organic light emitting device having at least a pair of electrodes consisting of an anode and a cathode, and a layer containing one or more organic compounds sandwiched between the pair of electrodes. In the above, at least one of the layers containing the organic compound is represented by the following general formula [3].
And at least one benzobisazomethine complex in which various diazole rings are condensed.

[0019]

[Chemical 6]

(In the formula, R ₄ is a hydrogen atom, a halogen atom, a nitro group, a nitrile group, a substituted silyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aralkyl group. Substituted or unsubstituted aryl group, substituted or unsubstituted amino group, substituted or unsubstituted azomethine group, substituted or unsubstituted carbonyl group, substituted or unsubstituted alkoxy group, substituted or unsubstituted ether group, substituted Alternatively, it is a group selected from the group consisting of unsubstituted heterocyclic groups.
r ₅ and Ar ₆ are a substituted or unsubstituted aryl group,
A group selected from a substituted or unsubstituted heterocyclic group,
It may be the same or different. Y ₅ and Y ₆ are
It is a group selected from the group consisting of an oxygen atom, a sulfur atom and a substituted or unsubstituted amino group, and may be the same or different. X ₃ is a sulfur atom, a sulfoxide,
It is a group selected from the group consisting of sulfone, oxygen atom and selenium atom, and may be the same or different. M ₃
Is a typical element such as Be, Ca, Mg, Sn, Ba, C
d, Co, Cr, Cu, Fe, Ni, Pb, Pd, P
The transition metal elements such as t, Sr, Ti, V, and Zn are shown. )

In the organic light emitting device of the present invention, X ₁ to
X ₃ is preferably a sulfur atom, a sulfoxide, or a sulfone.

[0022]

BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below.

First, the above general formula [1] to be used in the present invention.
The benzobisazomethine complex having a thiadiazole or various diazole rings condensed as the compound represented by [3] will be described.

Substituent R ₁ in the general formulas [1] to [3]
~R shows _4, a specific example of _{Ar 1 ~Ar 6, Y 1 ~Y} 6 below.

As the substituted silyl group, dimethylsilyl group, trimethylsilyl group, triethylsilyl group, triphenylsilyl group, ter-butyldimethylsilyl group, t
Examples thereof include, but are not limited to, er-butyldiphenylsilyl group and the like.

Examples of the substituted or unsubstituted alkyl group and aralkyl group include methyl group, ethyl group, n-propyl group, iso-propyl group, ter-butyl group, octyl group, benzyl group and phenethyl group. Of course, it is not limited to these.

Examples of the substituted or unsubstituted alkenyl group include vinyl group, allyl group (2-propenyl group), 1-propenyl group, iso-propenyl group and 2-butenyl group, but are not limited thereto. Not something.

Examples of the substituted or unsubstituted aryl group are phenyl group, 4-lithiumoxyphenyl group, 4-
Potassium oxyphenyl group, 4-cesium oxyphenyl group, 4-methylphenyl group, 4-ethylphenyl group,
3-chlorophenyl group, 3,5-dimethylphenyl group,
Triphenylamino group, biphenyl group, terphenyl group, naphthyl group, anthranyl group, phenanthryl group,
Examples thereof include a pyrenyl group and a ferrocenyl group, but are not limited to these. The substituted or unsubstituted amino group includes amino group, methylamino group, ethylamino group, dimethylamino group, diethylamino group, methylethylamino group, benzylamino group, methylbenzylamino group, anilino group, diphenylamino group, phenyl group. Examples thereof include a tolylamino group and a ditolylamino group, but are not limited thereto.

Examples of the substituted or unsubstituted azomethine group include methylimino group, ethylimino group, phenylimino group, (4-dimethylaminophenyl) imino group and (4-
(Cyanophenyl) imino group, (4-fluorophenyl)
Examples thereof include an imino group, a 2-pyridylimino group, a 9-anthranylimino group, and a 1-pyrenylimino group, but of course, the invention is not limited thereto.

Examples of the substituted or unsubstituted carbonyl group include an acetyl group, a propionyl group, an isobutyryl group, a methacryloyl group, a benzoyl group, a naphthoyl group, an anthryl group and a toluoyl group, but are not limited thereto. Absent.

Examples of the substituted or unsubstituted alkoxy group include a methoxy group, an ethoxy group, a propoxy group, a 2-ethyl-octyloxy group, a phenoxy group, a 4-butylphenoxy group, a benzyloxy group and the like. It is not limited to.

Examples of the substituted or unsubstituted ether group include methoxymethyl group, methoxydimethylmethyl group, methoxyethyl group, ethoxymethyl group, phenoxymethyl group and the like.

As the substituted or unsubstituted heterocyclic group,
Examples thereof include a pyridyl group, a bipyridyl group, a methylpyridyl group, a thienyl group, a terthienyl group, a propylthienyl group, a furyl group, a quinolyl group, a carbazolyl group, and an N-ethylcarbazolyl group, but are not limited thereto. Absent.

Examples of the substituted or unsubstituted aryl group and heterocyclic ring of Ar _{1 to} Ar ₆ include phenyl group, methylphenyl group, naphthyl group, pyridyl group, furyl group, thienyl group and quinolyl group. Of course, it is not limited to these.

The substituted or unsubstituted amino group represented by Y _{1 to} Y ₆ is an amino group, a methylamino group, an ethylamino group,
Examples thereof include a benzylamino group, a methylbenzylamino group, a phenylamino group and the like, but are not limited thereto.

Further, R _{1 to} R ₄ , Ar _{1 to} Ar ₆ , Y _{1 to} Y ₆
As the substituent which may have, a methyl group, an ethyl group,
Alkyl group such as n-propyl group, iso-propyl group, ter-butyl group, octyl group, benzyl group, phenethyl group, methoxy group, ethoxy group, propoxy group, 2-ethyl-octyloxy group, phenoxy group, 4- Alkoxy group such as butylphenoxy group, benzyloxy group, phenyl group, 4-methylphenyl group, 4-ethylphenyl group, 3-chlorophenyl group, 3,5-dimethylphenyl group, triphenylamino group, biphenyl group, terphenyl Group, naphthyl group, anthryl group, phenanthryl group,
Aryl group such as pyrenyl group, pyridyl group, bipyridyl group, methylpyridyl group, thienyl group, terthienyl group,
Examples thereof include heterocyclic groups such as a propylthienyl group, a furyl group, a quinolyl group, a carbazolyl group, and an N-ethylcarbazolyl group, but are not limited thereto.

Typical examples of the compounds represented by the general formulas [1] to [3] will be given below. However, it is not limited to these compounds. X _{1 to} X ₃ are groups selected from the group consisting of sulfur atom, sulfoxide, sulfone, oxygen atom and selenium atom, and may be the same or different. M _{1 to} M ₃ are Be, Ca, Mg, S
Typical elements such as n, Ba, Cd, Co, Cr, Cu, F
The transition metal elements such as e, Ni, Pb, Pd, Pt, Sr, Ti, V, and Zn are shown.

[0038]

[Chemical 7]

[0039]

[Chemical 8]

[0040]

[Chemical 9]

[0041]

[Chemical 10]

[0042]

[Chemical 11]

[0043]

[Chemical 12]

Next, the organic light emitting device of the present invention will be described with reference to the drawings.

FIG. 1 is a sectional view showing an example of the organic light emitting device of the present invention. FIG. 1 shows a structure in which an anode 2, a light emitting layer 3 and a cathode 4 are sequentially provided on a substrate 1. The light emitting device used here is useful when it has a single hole transporting ability, an electron transporting ability and a light emitting ability by itself, or when a compound having each characteristic is mixed and used.

FIG. 2 is a sectional view showing another example of the organic light emitting device of the present invention. In FIG. 2, an anode 2, a hole transport layer 5, an electron transport layer 6 and a cathode 4 are sequentially provided on a substrate 1. In this case, as the light emitting substance, a material having a hole transporting property, an electron transporting property, or both is used for each layer, and the light emitting substance is used in combination with a simple hole transporting substance or an electron transporting substance having no light emitting property. Useful in cases. In this case, the light emitting layer is composed of either the hole transport layer 5 or the electron transport layer 6.

FIG. 3 is a sectional view showing another example of the organic light emitting device of the present invention. FIG. 3 shows a structure in which an anode 2, a hole transport layer 5, a light emitting layer 3, an electron transport layer 6 and a cathode 4 are sequentially provided on a substrate 1. This separates the functions of carrier transport and light emission, and is used in combination with a compound having hole transporting property, electron transporting property, and light emitting property in a timely manner to greatly increase the degree of freedom in material selection and to increase the emission wavelength. Since various compounds having different colors can be used, it is possible to diversify the emission hue. Further, it becomes possible to effectively confine each carrier or exciton in the central light emitting layer 3 to improve the light emitting efficiency.

However, FIGS. 1 to 3 show only a very basic device structure, and the structure of the organic light emitting device using the compound of the present invention is not limited to these. For example, various layer configurations can be adopted such as providing an insulating layer at the interface between the electrode and the organic layer, providing an adhesive layer or an interference layer, and forming the hole transport layer from two layers having different ionization potentials.

General formulas [1] to [3] used in the present invention
The compounds represented by 1 are compounds having extremely excellent light emitting properties, electron injecting properties, and electron transporting properties as compared with conventional compounds, and any of the forms shown in FIGS. 1 to 3 can be used.

In particular, the organic layer using the compounds represented by the general formulas [1] to [3] of the present invention is useful as a light emitting layer and also as an electron transporting layer.

In the organic light emitting device of the present invention, at least one of the compounds represented by the general formulas [1] to [3] is formed between the anode 2 and the cathode 4 by the vacuum deposition method or the solution coating method. The thickness of the organic layer is less than 10 μm,
Preferably 0.5 μm or less, more preferably 0.05 to
It is preferable to reduce the thickness to 0.5 μm. Also,
It can be used together with the luminescent compound and the luminescent layer matrix compound which have been known so far.

In the present invention, the compounds represented by the above-mentioned general formulas [1] to [3] are used as the constituent components of the light emitting layer and the electron transport layer, and if necessary, hole transport known so far. Compounds, light-emitting compounds, light-emitting layer matrix compounds, electron-transporting compounds, charge-transporting polymer materials, and light-emitting polymer materials (for example, compounds shown below) can also be used together. However, of course, it is not limited to these.

[0053]

[Chemical 13]

[0054]

[Chemical 14]

[0055]

[Chemical 15]

[0056]

[Chemical 16]

[0057]

[Chemical 17]

[0058]

[Chemical 18]

In the organic light-emitting device of the present invention, the layer containing the compounds represented by the general formulas [1] to [3] and the layer containing other organic compounds are generally vacuum-deposited or dissolved in a suitable solvent. Then, a thin film is formed by a coating method. In particular, when the film is formed by the coating method, the film can be formed by combining with an appropriate binder resin.

The binder resin can be selected from a wide range of binder resins, such as polyvinyl carbazole resin,
Polycarbonate resin, polyester resin, polyarylate resin, polystyrene resin, acrylic resin, methacrylic resin, butyral resin, polyvinyl acetal resin,
Examples thereof include diallyl phthalate resin, phenol resin, epoxy resin, silicone resin, polysulfone resin, and urea resin, but are not limited thereto. Further, these may be used alone or as a copolymer polymer, or one or more kinds thereof may be mixed.

As the anode material, a material having a work function as large as possible is preferable. For example, simple metals such as gold, platinum, nickel, palladium, cobalt, selenium and vanadium or alloys thereof, tin oxide, zinc oxide, indium tin oxide ( A metal oxide such as ITO) or zinc indium oxide can be used. In addition, conductive polymers such as polyaniline, polypyrrole, polythiophene, and polyphenylene sulfide can also be used. These electrode substances may be used alone or in combination of two or more.

On the other hand, a material having a small work function is preferable as the cathode material, such as lithium, sodium, potassium, calcium, magnesium, aluminum, indium, silver,
It can be used as a simple metal or a plurality of alloys of lead, tin, chromium and the like. It is also possible to use a metal oxide such as indium tin oxide (ITO). The cathode may have a single layer structure or a multilayer structure.

The substrate used in the present invention is not particularly limited, but an opaque substrate such as a metal substrate or a ceramic substrate, or a transparent substrate such as glass, quartz or a plastic sheet is used. Further, it is also possible to control the emitted light by using a color filter film, a fluorescent color conversion filter film, a dielectric reflection film or the like on the substrate.

A protective layer or a sealing layer may be provided on the produced element for the purpose of preventing contact with oxygen or moisture. Examples of the protective layer include an inorganic material film such as a diamond thin film, a metal oxide and a metal nitride, a polymer film such as a fluorine resin, polyparaxylene, polyethylene, a silicone resin and a polystyrene resin, and a photocurable resin. To be It is also possible to cover the glass, gas impermeable film, metal, etc., and package the element itself with a suitable sealing resin.

[0065]

The present invention will be described in more detail with reference to the following examples, but the present invention is not limited thereto.

Example 1 An element having the structure shown in FIG. 3 was prepared.

On the glass substrate as the substrate 1, indium tin oxide (ITO) as the anode 2 was formed by sputtering 12
The film having a film thickness of 0 nm was used as a transparent conductive support substrate. This was sequentially ultrasonically cleaned with acetone and isopropyl alcohol (IPA), washed with boiling IPA, and dried. Furthermore, what was washed with UV / ozone was used as a transparent conductive support substrate.

As the hole transport material, N, N'-diphenyl-N, N'-m-tolyl-4,4'-diamino-1,
A solution adjusted to have a 1'-biphenyl (TPD) concentration of 0.5 wt% was dropped onto the anode 2, and spin coating was first performed at 500 RPM for 10 seconds and then at 1000 RPM for 1 minute. The film was formed. After this 10
The film was dried in a vacuum oven at 80 ° C. for 1 minute to completely remove the solvent in the thin film. The thickness of the formed TPD film (hole transport layer 5) was 50 nm.

Next, on the hole transport layer 5, tris (8-quinolinolato) aluminum (Alq3) was used as the host material of the light emitting layer 3, and the above exemplified compound No. 3 was used as the dopant. 1 (X ₁ = S, M ₁ = Zn) co-evaporated to 20 nm
Was provided. The film deposition rate is 0.3 nm for the host
Co-deposition was performed while adjusting the sec and the dopant to be 0.1 nm / sec.

Further, Alq3 was formed as the electron transport layer 6 in a film thickness of 40 nm by the vacuum evaporation method. The degree of vacuum at the time of vapor deposition of these organic layers is 4.0 × 10 ⁻⁴ Pa, and the film formation rate is 0.1.
The condition was 3 nm / sec.

Next, using a vapor deposition material made of an aluminum-lithium alloy (lithium concentration: 1 atomic%), a metal layer film having a thickness of 10 nm was formed on the above organic layer by a vacuum vapor deposition method, and further a vacuum was formed. An aluminum film having a thickness of 150 nm was provided by an evaporation method to form an aluminum-lithium alloy film (cathode 4). The degree of vacuum during vapor deposition is 1.0 x 10
^The film was formed under the conditions of ⁻⁴ Pa and a film forming rate of 1.0 to 1.2 nm / sec.

The obtained organic EL device was covered with a protective glass plate in a dry air atmosphere and sealed with an acrylic resin adhesive so that the device would not be deteriorated by adsorption of water.

The emission spectrum of the obtained device was 650 n.
Red with a peak at m and brightness of 240 cd / m at 9V
² , 380 cd / m ² at 12V.

Further, the current density is set to 250 in a nitrogen atmosphere.
When the voltage was applied for 100 hours while keeping at mA / cm ² ,
Initial brightness of 180 cd / m ² to 160 cd after 100 hours
The brightness deterioration was as small as / m ² .

Example 2 Exemplified Compound No. 1 (X ₁ =
S, M ₁ = Zn) in place of Exemplified Compound No. 1 (X ₁ =
A device was prepared in the same manner as in Example 1 using S and M ₁ = Pt), and the same evaluation was performed.

The emission spectrum of the obtained device is 660.
Red with a peak at nm and luminance of 220 cd / 9V
The brightness was 365 cd / m ² at m ² and 12 V.

Further, the current density is set to 250 in a nitrogen atmosphere.
When the voltage was applied for 100 hours while keeping at mA / cm ² ,
Initial brightness of 165 cd / m ² to 140 cd after 100 hours
The brightness deterioration was as small as / m ² .

Example 3 Exemplified Compound No. 1 (X ₁ =
S, M ₁ = Zn) in place of Exemplified Compound No. 1 (X ₁ =
A device was prepared in the same manner as in Example 1 using SO ₂ and M ₁ = Zn), and the same evaluation was performed.

The emission spectrum of the obtained device is 675.
Red with a peak at nm and brightness of 200 cd / at 9V
The brightness was 320 cd / m ² at m ² and 12 V.

Further, the current density is set to 250 in a nitrogen atmosphere.
When the voltage was applied for 100 hours while keeping at mA / cm ² ,
Initial brightness of 130 cd / m ² to 110 cd after 100 hours
The brightness deterioration was as small as / m ² .

Example 4 Exemplified Compound No. 1 (X ₁ =
S, M ₁ = Zn) in place of Exemplified Compound No. 11 (X ₁
= S, M ₁ = Zn), an element was prepared in the same manner as in Example 1, and the same evaluation was performed.

The emission spectrum of the obtained device was 680.
Red with a peak at nm and brightness of 170 cd / at 9V
The brightness was 280 cd / m ² at m ² and 12 V.

Further, the current density is set to 250 in a nitrogen atmosphere.
When the voltage was applied for 100 hours while keeping at mA / cm ² ,
Initial brightness of 100 cd / m ² to 85 cd / 100 hours later
The brightness deterioration was small with m ² .

Example 5 Exemplified Compound No. 1 (X ₁ =
S, M ₁ = Zn) in place of Exemplified Compound No. 14 (X ₁
= S, M ₁ = Zn), an element was prepared in the same manner as in Example 1, and the same evaluation was performed.

The emission spectrum of the obtained device is 685.
Red with a peak at nm, brightness of 9 cd at 160 cd /
The brightness was 265 cd / m ² at m ² and 12 V.

Further, the current density was set to 250 in a nitrogen atmosphere.
When the voltage was applied for 100 hours while keeping at mA / cm ² ,
Initial brightness of 85 cd / m ² to 70 cd / m ² after 100 hours
And the brightness deterioration was small.

Example 6 Exemplified Compound No. 1 (X ₁ =
S, M ₁ = Zn) in place of Exemplified Compound No. 19 (X ₂
= S, M ₂ = Zn), an element was prepared in the same manner as in Example 1, and the same evaluation was performed.

The emission spectrum of the obtained device is 665.
Red with a peak at nm and brightness of 240 cd / 9V
The brightness was 370 cd / m ² at m ² and 12 V.

Further, the current density is set to 250 in a nitrogen atmosphere.
When the voltage was applied for 100 hours while keeping at mA / cm ² ,
Initial brightness of 170 cd / m ² to 150 cd after 100 hours
The brightness deterioration was as small as / m ² .

Example 7 Exemplified Compound No. 1 (X ₁ =
S, M ₁ = Zn) in place of Exemplified Compound No. 37 (X ₃
= S, M ₃ = Zn), an element was prepared in the same manner as in Example 1, and the same evaluation was performed.

The emission spectrum of the obtained device is 663.
Red with a peak at nm, brightness of 245 cd / 9V
The brightness was 370 cd / m ² at m ² and 12 V.

Further, the current density is set to 250 in a nitrogen atmosphere.
When the voltage was applied for 100 hours while keeping at mA / cm ² ,
Initial brightness of 180 cd / m ² to 155 cd after 100 hours
The brightness deterioration was as small as / m ² .

Comparative Example 1 Exemplified Compound No. 1 (X ₁ =
S, M ₁ = Zn) was used, and a device was prepared in the same manner as in Example 1 using the comparative compound having the following structural formula, and the same evaluation was carried out. Was obtained.

[0094]

[Chemical 19]

[0095]

The organic light emitting device using the compounds represented by the general formulas [1] to [3] of the present invention exhibits a red light emission hue at a low applied voltage as shown in Examples and Comparative Examples. It also has excellent durability.

In particular, the organic layer using the compound represented by the general formula [1] of the present invention is useful as a light emitting layer and also as an electron transporting layer.

Further, the element can be formed by using the vacuum evaporation method or the casting method, and the element having a large area can be easily prepared at a relatively low cost.

[Brief description of drawings]

FIG. 1 is a cross-sectional view showing an example of an organic light emitting device according to the present invention.

FIG. 2 is a cross-sectional view showing another example of the organic light emitting device according to the present invention.

FIG. 3 is a cross-sectional view showing another example of the organic light emitting device according to the present invention.

[Explanation of symbols]

1 substrate 2 anode 3 light emitting layer 4 cathode 5 hole transport layer 6 Electron transport layer

   ─────────────────────────────────────────────────── ─── Continued front page    (72) Inventor Hiroshi Tanabe             3-30-2 Shimomaruko, Ota-ku, Tokyo             Non non corporation F-term (reference) 3K007 AB02 AB03 AB04 AB11 DB03

Claims (6)

[Claims] 1. A pair of electrodes comprising an anode and a cathode,
In an organic light emitting device having at least a layer containing one or a plurality of organic compounds sandwiched between the pair of electrodes, at least one of the layers containing an organic compound is a thiadiazole represented by the following general formula [1] or various compounds. An organic light-emitting device comprising at least one benzobisazomethine complex in which the diazole ring is condensed. [Chemical 1] (In the formula, R ₁ and R ₂ are a hydrogen atom, a halogen atom, a nitro group, a nitrile group, a substituted silyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group,
Substituted or unsubstituted aralkyl group, substituted or unsubstituted aryl group, substituted or unsubstituted amino group, substituted or unsubstituted azomethine group, substituted or unsubstituted carbonyl group, substituted or unsubstituted alkoxy group, substituted or It is a group selected from the group consisting of an unsubstituted ether group and a substituted or unsubstituted heterocyclic group. Ar ₁ and Ar ₂ are groups selected from a substituted or unsubstituted aryl group and a substituted or unsubstituted heterocyclic group, and may be the same or different. Y ₁ and Y ₂ are groups selected from the group consisting of oxygen atom, sulfur atom and substituted or unsubstituted amino group, and may be the same or different. X ₁ is a group selected from the group consisting of sulfur atom, sulfoxide, sulfone, oxygen atom and selenium atom, and may be the same or different. M ₁ is B
e, Ca, Mg, Sn and other typical elements, Ba, Cd, C
o, Cr, Cu, Fe, Ni, Pb, Pd, Pt, S
The transition metal elements such as r, Ti, V, and Zn are shown. ) 2. A pair of electrodes consisting of an anode and a cathode,
In an organic light emitting device having at least a layer containing one or a plurality of organic compounds sandwiched between the pair of electrodes, at least one of the layers containing an organic compound is thiadiazole represented by the following general formula [2] or various kinds. An organic light-emitting device comprising at least one benzobisazomethine complex in which the diazole ring is condensed. [Chemical 2] (In the formula, R ₃ is a hydrogen atom, a halogen atom, a nitro group,
Nitrile group, substituted silyl group, substituted or unsubstituted alkyl group, substituted or unsubstituted alkenyl group, substituted or unsubstituted aralkyl group, substituted or unsubstituted aryl group, substituted or unsubstituted amino group, substituted or unsubstituted It is a group selected from the group consisting of a substituted azomethine group, a substituted or unsubstituted carbonyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted ether group, and a substituted or unsubstituted heterocyclic group. Ar ₃ and Ar
₄ is a group selected from a substituted or unsubstituted aryl group and a substituted or unsubstituted heterocyclic group, which may be the same or different. Y ₃ and Y ₄ are groups selected from the group consisting of oxygen atom, sulfur atom, and substituted or unsubstituted amino group, and may be the same or different. X ₂ is a group selected from the group consisting of sulfur atom, sulfoxide, sulfone, oxygen atom and selenium atom,
It may be the same or different. M ₂ is Be, C
a, Mg, Sn and other typical elements, Ba, Cd, Co, C
r, Cu, Fe, Ni, Pb, Pd, Pt, Sr, T
The transition metal elements such as i, V, and Zn are shown. ) 3. A pair of electrodes consisting of an anode and a cathode,
In an organic light-emitting device having at least a layer containing one or more organic compounds sandwiched between the pair of electrodes, at least one of the layers containing the organic compound is thiadiazole represented by the following general formula [3] or various An organic light-emitting device comprising at least one benzobisazomethine complex in which the diazole ring is condensed. [Chemical 3] (In the formula, R ₄ is a hydrogen atom, a halogen atom, a nitro group,
Nitrile group, substituted silyl group, substituted or unsubstituted alkyl group, substituted or unsubstituted alkenyl group, substituted or unsubstituted aralkyl group, substituted or unsubstituted aryl group, substituted or unsubstituted amino group, substituted or unsubstituted It is a group selected from the group consisting of a substituted azomethine group, a substituted or unsubstituted carbonyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted ether group, and a substituted or unsubstituted heterocyclic group. Ar ₅ and Ar
₆ is a group selected from a substituted or unsubstituted aryl group and a substituted or unsubstituted heterocyclic group, which may be the same or different. Y ₅ and Y ₆ are groups selected from the group consisting of oxygen atom, sulfur atom and substituted or unsubstituted amino group, and may be the same or different. X ₃ is a group selected from the group consisting of sulfur atom, sulfoxide, sulfone, oxygen atom and selenium atom,
It may be the same or different. M ₃ is Be, C
a, Mg, Sn and other typical elements, Ba, Cd, Co, C
r, Cu, Fe, Ni, Pb, Pd, Pt, Sr, T
The transition metal elements such as i, V, and Zn are shown. ) 4. X _{1 to} X _{3 in the} general formulas [1] to [3].
Is a sulfur atom, The organic light emitting element in any one of Claims 1-3 characterized by the above-mentioned. 5. In the general formulas [1] to [3], X _{1 to} X ₃
Is a sulfoxide, The organic light emitting element in any one of Claims 1-3 characterized by the above-mentioned. 6. X _{1 to} X _{3 in the} general formulas [1] to [3].
Is a sulfone, The organic light emitting element in any one of Claims 1-3 characterized by the above-mentioned.