JP4317476B2 - Organic EL device and organic EL display - Google Patents

Description

  The present invention relates to an organic EL (electroluminescence, electroluminescence) element and an organic EL display.

  In the field of organic EL elements used for organic EL displays and the like, various types of devices have been prototyped based on a technique for forming an organic layer using a low molecular weight compound by a vacuum deposition method (for example, see Non-Patent Document 1). It is about to reach the stage of conversion.

On the other hand, development of an organic EL element using a polymer material as a constituent material of the organic layer is underway. Such an organic EL element generally has a π-conjugated type using a π-conjugated polymer (for example, see Patent Document 1) and a molecular dispersion type in which a dye is dispersed in a non-conjugated polymer. (See, for example, Non-Patent Documents 2 and 3). Among these, the non-conjugated organic EL device has an advantage that a desired color can be obtained with high color purity by mixing a predetermined dopant into the host polymer.
Japanese Patent Laid-Open No. 10-92576 Applied Physics Letters, vol. 51, p913 (1987) Polymer, vol. 24, p748 (1983) Applied Physics Letters, vol. 75, no. 1, p4 (1999)

  However, recently, further improvement in the element characteristics of the organic EL element has been demanded, and there is still room for improvement in order to meet such a demand even with the conventional organic EL element. In particular, in the case of a conventional organic EL device using a non-π conjugated polymer, the lifetime is not sufficient, and device characteristics such as light emission efficiency are degraded in a relatively short time.

  The present invention has been made in view of the above-mentioned problems of the prior art, and provides a long-life organic EL element and an organic EL display capable of maintaining element characteristics such as luminous efficiency at a high level over a long period of time. The purpose is to do.

  As a result of intensive studies to achieve the above object, the present inventors have found that the above problems can be solved by using a vinyl polymer having a specific structural unit as a constituent material of the organic layer. It came to be completed.

  That is, the organic EL device of the present invention includes a pair of electrodes arranged to face each other, an organic layer containing a vinyl polymer that is disposed between the electrodes and has a structural unit represented by the following formula (I): It is characterized by providing.

[In formula (I), X represents a divalent organic group, L represents a (p + 2) valent aromatic group having 6 to 13 carbon atoms , and Y, R ¹ and R ² are each independently a monovalent group. A represents a substituent, a represents an integer of 0 to 8, b represents an integer of 0 to 9, p represents 0 or an integer of 1 or more, and n represents an integer of 1 or more. ]
In the organic EL device of the present invention, by including the specific vinyl polymer in the organic layer, the heat resistance and electric resistance characteristics of the organic layer, and the adhesion with the adjacent layer can be sufficiently improved. Therefore, according to the present invention, it is possible to realize a long-life organic EL element capable of maintaining element characteristics such as light emission efficiency and light emission luminance at a high level even when driven for a long time or repeatedly.

  Although the reason why the above-described effect can be obtained by the present invention is not necessarily clear, the present inventors infer as follows. That is, the vinyl polymer according to the present invention has a structure in which two anthracene skeletons are linked via a divalent linking group L, so that adequate flexibility is maintained while sufficiently maintaining characteristics such as carrier transportability. Is considered to be given. And by including such a vinyl polymer in the organic layer, driving of the organic EL element (application of voltage) and driving stop, and further, embrittlement of the organic layer with respect to the temperature change associated therewith can be effectively suppressed, It is considered that the organic EL element can have a sufficiently long life.

  In the organic EL device of the present invention, the aromatic group represented by L in the vinyl polymer is preferably a phenylene group, a naphthylene group, a biphenylylene group, a fluorenylene group, or a carbazolylene group. In this case, it is considered that the flexibility of the vinyl polymer is further improved and the resistance of the organic layer to temperature change is further improved. Therefore, the lifetime of the organic EL element can be further increased.

  In the organic EL device of the present invention, the structural unit represented by the formula (I) in the vinyl polymer is preferably a structural unit represented by the following formula (I-1).

[In Formula (I-1), X represents a divalent organic group, L represents a (p + 2) -valent aromatic group having 6 to 13 carbon atoms , and Y, R ¹ , R ³ and R ⁴ are each Independently represents a monovalent substituent, a represents an integer of 0 to 8, c represents an integer of 1 to 9, p represents 0 or an integer of 1 or more, and n represents an integer of 1 or more. ]
In this case, since the stability of the vinyl polymer is particularly excellent, it is considered that the resistance of the organic layer to temperature change is further improved. Therefore, the lifetime of the organic EL element can be further increased.

  In addition, since the vinyl polymer concerning this invention has luminescent property, the organic layer does not need to contain the dopant for light emission, In order to obtain a desired light emission color, the organic layer further contains a light emitting dopant, A vinyl polymer having a structural unit represented by the general formula (I) is preferably used as the host material.

  Moreover, the organic EL display of the present invention includes a pair of electrodes arranged to face each other, an organic layer containing a vinyl polymer that is disposed between the electrodes and has a structural unit represented by the above formula (I), A plurality of organic EL elements each having a plurality of organic EL elements are electrically connected to each of the pair of electrodes, and a power supply section that supplies a voltage or current to the electrodes, and each of the organic EL elements is turned on or The switching part which turns off is provided, It is characterized by the above-mentioned.

  In this way, by arranging the organic EL elements of the present invention in the display unit and further driving the display unit by the power supply unit and the switching unit, an organic EL display having excellent luminance and color display functions and a long life can be obtained. It becomes feasible.

  ADVANTAGE OF THE INVENTION According to this invention, the long-life organic EL element and organic EL display which can maintain element characteristics, such as luminous efficiency, at a high level over a long period of time are provided.

  Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the drawings as the case may be. In the drawings, the same elements are denoted by the same reference numerals, and redundant description is omitted. Further, the positional relationship such as up, down, left and right is based on the positional relationship shown in the drawings unless otherwise specified. Further, the dimensional ratios in the drawings are not limited to the illustrated ratios.

  First, the vinyl polymer contained in the organic layer in the organic EL device of the present invention will be described. The vinyl polymer according to the present invention has a structural unit represented by the following formula (I).

Here, in the formula (I), X represents a divalent organic group, L represents a divalent aliphatic hydrocarbon group having 1 to 4 carbon atoms, and a (p + 2) valent aromatic group having 6 to 13 carbon atoms. Or an imino group, Y, R ¹ and R ² each independently represents a monovalent substituent, a represents an integer of 0 to 8 (more preferably 0 to 4), and b represents 0 to 9 ( More preferably, it represents an integer of 0 to 4), p represents 0 or an integer of 1 or more, and n represents an integer of 1 or more.

  In the above formula (I), X is preferably a divalent hydrocarbon group among divalent organic groups, more preferably a divalent aromatic hydrocarbon group, and a divalent C 6-13 divalent. The aromatic hydrocarbon group is more preferable.

  L is preferably a (p + 2) -valent aromatic group having 6 to 13 carbon atoms among the divalent groups described above. If the aromatic group has more than 13 carbon atoms, the molecular structure becomes rigid, the vinyl polymer is easily crystallized, and the wavelength range of the emission color is shifted to change the emission color. The aromatic group may be a hydrocarbon group or a heterocyclic group, but is more preferably a phenylene group, a naphthylene group, a biphenylylene group, a fluorenylene group, or a carbazolylene group, and further preferably a phenylene group or a naphthylene group. Preferable is a phenylene group.

  When L is an imino group (—NH—), when p is 0, L is an imino group (—NH—), and when p is 1, L is a divalent group represented by —NY—. is there.

  In the structural unit represented by the above formula (I), X and L are bonded to the 9th and 10th positions in the anthracene skeleton, respectively, so that the molecular structure is excellent in stability.

Y is preferably a hydrocarbon group, more preferably an aliphatic hydrocarbon group or an aromatic hydrocarbon group, and further preferably an aliphatic hydrocarbon group or an aromatic hydrocarbon group having 1 to 6 carbon atoms. Moreover, as an aromatic hydrocarbon group, a phenyl group or a naphthyl group is preferable, and a phenyl group is more preferable. In the divalent group represented by L- (Y) _p , p is more preferably 0.

R ¹ and R ² are each independently preferably an alkyl group, an alkoxy group, an aryl group, an aryloxy group, a heterocyclic group, a halogen atom, a cyano group, a hydroxyl group, or an amino group. The groups may be bonded to each other to form a ring.

When R ¹ and R ² are alkyl groups, the alkyl group may be linear or branched. The alkyl group is preferably unsubstituted, but may have a substituent. As for carbon number of an alkyl group, 1-30 are preferable. Preferred alkyl groups include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, s-butyl, t-butyl, pentyl and the like.

When R ¹ and R ² are alkoxy groups, the alkyl group constituting the alkoxy group may be linear or branched. The alkoxy group is preferably unsubstituted, but may have a substituent. As for carbon number of an alkoxy group, 1-30 are preferable. Preferred alkoxy groups include methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, s-butoxy, t-butoxy and the like.

When R ¹ and R ² are aryl groups, the aryl group may be substituted or unsubstituted, but the total carbon number of the aryl group is preferably 6-20. Preferable aryl groups include phenyl group, o-tolyl group, m-tolyl group, p-tolyl group, biphenylyl group and the like.

When R ¹ and R ² are aryloxy groups, the aryl group constituting the aryloxy group may be substituted or unsubstituted, but the total number of carbon atoms of the aryloxy group is preferably 6-20. Preferred aryloxy groups include phenoxy group, o-tolyloxy group, m-tolyloxy group, p-tolyloxy group and the like.

When R ¹ and R ² are heterocyclic groups, the heterocyclic group is preferably a 5-membered ring group or a 6-membered ring group. The heterocyclic group may have a condensed ring and may have a substituent. The heterocyclic group may have aromaticity or may not have aromaticity. Preferable heterocyclic groups include pyrrolyl group, pyridyl group, quinolyl group, thienyl group, furyl group and the like.

When R ¹ and R ² are halogen atoms, examples of the halogen atom include fluorine, chlorine, bromine, iodine and the like.

When R ¹ and R ² are amino groups, the amino group may be substituted or unsubstituted, and may have, for example, the above-described alkyl group or aryl group. As for the total carbon number of an amino group, 0-20 are preferable. Preferred amino groups include a narrowly defined amino group (—NH ₂ ), a methylamino group, an ethylamino group, a phenylamino group, a dimethylamino group, and a diphenylamino group.

In the structural unit represented by the above formula (I), at least one R ² exists and is bonded to the 10th position of the anthracene skeleton, that is, represented by the following formula (I-1). A structural unit is preferred.

Here, in the formula (I-1), X represents a divalent organic group, L represents a divalent aliphatic hydrocarbon group having 1 to 4 carbon atoms, and a (p + 2) valent aroma having 6 to 13 carbon atoms. A group, or an imino group, Y, R ¹ , R ³ and R ⁴ each independently represents a monovalent substituent, a represents an integer of 0 to 8 (more preferably 0 to 4), c Represents an integer of 1 to 9 (more preferably 1 to 4), p represents 0 or an integer of 1 or more, and n represents an integer of 1 or more.

In the formula (I-1), X, L, Y and ^{R 1} are as defined X, L, and Y and ^{R 1} in the formula (I), ^{R 3} and ^{R 4} are ^{R 1} as defined It is. As the ^{R 3,} aryl group, more preferably an aryl group having 6 to 18 carbon atoms.

  Specific examples of suitable structural units represented by the above formula (I) include structural units represented by the following (I-1-1) to (I-1-13). In the following formula, n represents an integer of 1 or more.

  The vinyl polymer according to the present invention described above can be obtained by polymerizing a polymerizable monomer as a raw material by each polymerization method. The vinyl polymer according to the present invention preferably has a weight average molecular weight of 10,000 to 1,000,000.

  Next, the organic EL element of the present invention will be described.

  FIG. 1 is a schematic cross-sectional view showing a preferred embodiment of the organic EL device of the present invention. In the organic EL element 9 shown in FIG. 1, the anode layer 2 (first electrode layer) and the insulator layer 6 are laminated in this order on the substrate 1, and correspond to the light emitting region of the insulator layer 6. An opening is provided in the portion where the anode layer 2 is exposed. Then, the organic layer 3 and the cathode layer 4 (second electrode layer) are laminated in this order on the exposed anode layer 2, and the laminated structure of substrate 1 / anode layer 2 / organic layer 3 / cathode layer 4 is obtained. Is formed. The organic layer 3 contains a vinyl polymer having a structural unit represented by the above formula (I). The surface of the organic EL element 9 on the cathode layer 2 side is sealed with a sealing plate 5 via a spacer 7 provided on the insulator layer 6 in the non-light emitting region.

(substrate)
As the substrate 1, an amorphous substrate such as glass or quartz, a crystal substrate such as Si, GaAs, ZnSe, ZnS, GaP, or InP, or a metal substrate such as Mo, Al, Pt, Ir, Au, Pd, or SUS is used. Can be used. In addition, a thin film made of crystalline or amorphous ceramic, metal, organic material or the like formed on a predetermined substrate may be used.

  When the substrate 1 side is the light extraction side, it is preferable to use a transparent substrate such as glass or quartz as the substrate 1, and it is particularly preferable to use an inexpensive glass transparent substrate. The transparent substrate may be provided with a color filter film, a color conversion film containing a fluorescent material, a dielectric reflection film, or the like for adjusting the color light.

(Anode layer)
The anode layer 2 functions as a hole injection electrode to the organic layer 3. Therefore, the material of the anode layer 2 is preferably a material that can efficiently inject holes into the organic layer, and more specifically a material having a work function of 4.5 to 5.5 eV.

  Further, when the substrate 1 side is the light extraction side, the transmittance at a wavelength of 400 to 700 nm, which is the emission wavelength region of the organic EL element, particularly the transmittance at the wavelength of each RGB color is preferably 50% or more, It is more preferably 80% or more, and further preferably 90% or more. If the transmittance of the anode layer 2 is less than 50%, the light emission from the organic layer 3 is attenuated and it is difficult to obtain the luminance necessary for image display.

The anode layer 2 having a high light transmittance can be configured using a transparent conductive film composed of various oxides. As such a material, indium oxide (In ₂ O ₃ ), tin oxide (SnO ₂ ), zinc oxide (ZnO), tin-doped indium oxide (ITO), zinc-doped indium oxide (IZO), and the like are preferable. It is particularly preferable in that a thin film having a uniform in-plane specific resistance can be easily obtained. The ratio of SnO ₂ to In ₂ O _{3 in} ITO is preferably 1 to 20% by weight, and more preferably 5 to 12% by weight. The ratio of ZnO to In ₂ O ₃ in IZO is preferably 12 to 32% by weight. The said material may be used individually by 1 type, and may be used in combination of 2 or more type.

Note that the composition of the oxide constituting the anode layer 2 may be somewhat deviated from the stoichiometric composition. For example, ITO usually contains In ₂ O ₃ and SnO _{2 in a} stoichiometric composition, but when the composition of ITO is represented by InO _x · SnO _y , x is in the range of 1.0 to 2.0. , Y may be in the range of 0.8 to 1.2.

Further, the work function of the anode layer 2 can be adjusted by adding a transparent dielectric such as silicon oxide (SiO ₂ ) to the anode layer 2. For example, the work function of ITO can be increased by adding about 0.5 to 10 mol% of SiO ₂ with respect to ITO, and the work function of anode layer 2 can be within the above-mentioned preferable range.

  The film thickness of the anode layer 2 is preferably determined in consideration of the above light transmittance. For example, when using an oxide transparent conductive film, the film thickness is preferably 50 to 500 nm, more preferably 50 to 300 nm. When the thickness of the anode layer 2 exceeds 500 nm, the light transmittance becomes insufficient and the anode layer 2 may be peeled off from the substrate 1 in some cases. Further, the light transmittance is improved as the film thickness is reduced. However, when the film thickness is less than 50 nm, the efficiency of hole injection into the organic layer 3 is lowered and the strength of the film is lowered.

  FIG. 1 shows an example of an organic EL element in which the anode layer 2 is disposed on the substrate 1 and the cathode layer 4 is disposed on the side far from the substrate 1 with the organic layer 3 interposed therebetween. The position of the layer 4 may be reversed. When the cathode layer 4 is disposed on the substrate 1, the cathode layer 4 side can be the light extraction side. In this case, the cathode layer 4 preferably satisfies the optical conditions and film thickness conditions described above. .

(Insulator layer)
In the organic EL device of the present invention, it is preferable to provide an insulator layer 6 in the non-light emitting region on the anode layer 2 as shown in FIG. By providing the insulating layer 6, it is possible to control the light emission area and suppress color bleeding. As a material of the insulating layer 6, a general insulating film material such as SiO ₂ or Al ₂ O ₃ can be appropriately selected and used. The thickness of the insulator layer 6 is preferably about 1 to 7 μm. An opening is provided in a portion corresponding to the light emitting region of the insulator layer 6 by photolithography and etching so that the anode layer 2 is exposed. On the exposed anode layer 2, an organic layer 3 and a cathode layer are provided. 4 (second electrode layers) are laminated in this order. Thereby, electrical conduction between the anode layer 2 and the organic layer 3 is ensured.

(Organic layer)
As described above, the organic layer 3 contains the vinyl polymer according to the present invention, and may further contain a light emitting dopant.

Here, the light emitting dopant can be appropriately selected according to the intended emission color. For example, as a phosphorescent dopant, an iridium complex such as tris (2-phenylpyridine) iridium (Ir (ppy) ₃ ), 2,3,7,8,12,13,17,18-octaethyl-21H, 23H-porphyrin A platinum complex having a porphyrin ring such as platinum (PtOEP) can be used. Further, as the blue light emitting dopant, tetraphenylbutadiene and its derivatives, styrylamine derivatives, fluoranthene derivatives and the like can be used. The proportion of the light emitting dopant is preferably 1 to 15% by weight with respect to the total amount of the polymerizable monomer before polymerizing the polymer.

  The organic layer 3 may have either a single layer structure or a multilayer structure. In the case of a multilayer structure, any one of a plurality of layers constituting the organic layer 3 may contain the vinyl polymer according to the present invention.

  For example, a hole transport layer is disposed between the light-emitting layer and the anode layer, an electron transport layer is disposed between the light-emitting layer and the cathode layer, and the hole transport layer / light-emitting layer / electron transport layer is formed in the order from the anode layer. It can be set as the organic layer of the multilayered structure laminated | stacked. Thereby, the injection ability of holes and electrons injected from the anode layer and the cathode layer into the light emitting layer and the mobility of these charges can be controlled. In such an organic layer having a multilayer structure, it is preferable that one or both of the light emitting layer and the carrier transport layer contain the vinyl polymer according to the present invention. Thereby, the lifetime improvement of an organic EL element can be achieved.

  The organic layer according to the present invention may have an electron blocking layer between the light emitting layer and the anode layer, and a hole blocking layer between the light emitting layer and the cathode layer. These carrier block layers can be formed using a polymer to be described later, or further using a hole transporting material or an electron transporting material.

  Further, light emission from a plurality of layers can be obtained by adding a light emitting dopant to the carrier block layer to form a light emitting layer / carrier block layer and laminating the light emitting layer separately provided.

  The organic layer 3 may further contain a light emitting material in addition to the materials described above. Examples of the light emitting material include a vinyl polymer according to the present invention, a polyparaphenylene vinyl structure, a polyparaphenylene structure, a polyamine structure, a polythiophene structure, a polyfluorene structure, a π-conjugated polymer, a benzene ring structure, and a naphthalene ring structure. And anthracene ring structure, diphenylnaphthacene ring structure, pyrene ring structure, phenanthrene ring structure, phenanthroline ring structure, fluoranthene ring structure, vinyl polymer having a fluorene ring structure (non-π conjugated polymer), and the like.

  The organic layer 3 may further contain other carrier transport materials such as a hole transport material and an electron transport material.

  As the hole transporting material, either a low molecular material or a high molecular material can be used. Examples of the hole transporting low molecular weight material include pyrazoline derivatives, arylamine derivatives, stilbene derivatives, and triphenyldiamine derivatives. Examples of the hole transporting polymer material include polyvinyl carbazole, polyethylene dioxythiophene / polystyrene sulfonic acid copolymer (PEDOT / PSS), polyaniline / polystyrene sulfonic acid copolymer (Pani / PSS), and the like. One of these hole transport materials may be used alone, or two or more thereof may be used in combination.

  As the electron transporting material, either a low molecular material or a high molecular material can be used. Examples of the electron transporting low molecular weight material include oxadiazole derivatives, anthraquinodimethane and derivatives thereof, benzoquinone and derivatives thereof, naphthoquinone and derivatives thereof, anthraquinones and derivatives thereof, tetracyanoanthraquinodimethane and derivatives thereof, and fluorene. And derivatives thereof, diphenyldicyanoethylene and derivatives thereof, phenanthroline and derivatives thereof, and metal complexes having these compounds as ligands. Examples of the electron transporting polymer material include polyquinoxaline and polyquinoline. One of these electron transporting materials may be used alone, or two or more thereof may be used in combination.

  As for the low molecular weight material and its usage, for example, JP-A-63-70257, JP-A-63-175860, JP-A-2-135359, JP-A-3-37992, JP-A-3-37792. The technique disclosed in Japanese Patent Laid-Open No. 3-152184 can be used.

  The organic layer 3 can be suitably formed by a coating method. In such coating, a coating solution obtained by adding the constituent material of the target layer to a predetermined solvent is used. For example, when forming a light emitting layer, the coating liquid which added the vinyl polymer concerning this invention and the dopant for light emission to the predetermined | prescribed solvent as needed is used. A solvent will not be specifically limited if the vinyl polymer concerning this invention melt | dissolves and a disorder | damage | failure does not arise at the time of application | coating. For example, organic solvents such as alcohols, hydrocarbons, ketones, and ethers can be used. Of these, chloroform, methylene chloride, dichloroethane, tetrahydrofuran, toluene, xylene, cyclohexanone, dimethylformamide, N-methylpyrrolidone, and the like are preferable. The amount of the vinyl polymer according to the present invention dissolved in the solvent is appropriately selected according to the structure and molecular weight of the vinyl polymer, but is preferably 0.1% by weight or more.

  The coating solution thus prepared is applied so as to cover the opening of the insulating layer 6 where the anode layer 2 is exposed, and the solvent is removed from the coating solution. The organic layer 3 is formed by sequentially performing this coating and solvent removal for each constituent layer of the organic layer. A coating method for the coating solution is not particularly limited, and for example, a spin coating method, a spray coating method, a dip coating method, an ink jet method, a printing method, and the like are applicable. Moreover, the removal of the solvent from a coating liquid can be performed by heat-drying under the pressure reduction or inert gas atmosphere, Preferably it is 30-200 degreeC, More preferably, it is the temperature of 60-100 degreeC.

  The film thickness of the organic layer 3 is not particularly limited, and varies depending on the forming method, but is preferably 5 to 500 nm, more preferably 10 to 300 nm.

(Cathode layer)
The cathode layer 4 functions as a layer for injecting electrons into the organic layer 3. Specific examples of the cathode layer 4 include an inorganic electron injection layer, an electron injection layer composed of a coating film of an organometallic complex, and an electron injection layer composed of a coating film of a metal salt. A laminate in which an auxiliary electrode layer is laminated on these electron injection layers may be used as the cathode layer 4. In the case of such a laminate, the inorganic electron injection layer, the coating film of the organometallic complex, and the coating film of the metal salt are disposed on the side close to the organic layer 3, and the auxiliary electrode layer is disposed on the side far from the organic layer 3.

  When forming an inorganic electron injection layer, it is preferable to select an inorganic material having a low work function so that electron injection into the organic layer 3 is facilitated. Examples of such inorganic materials include alkali metals such as Li, Na, K, and Cs, alkaline earth metals such as Mg, Ca, Sr, and Ba, and alkali halides such as LiF and CsI. Alternatively, a metal having properties similar to those of an alkali metal or an alkaline earth metal such as La, Ce, Sn, Zn, or Zr can be used. Among these, Ca is particularly preferable because it has a very low work function.

  The film thickness of the inorganic electron injection layer is not particularly limited as long as electrons can be injected into the organic layer 3, but preferably 0.1 to 100 nm, more preferably 1 when an alkali metal or an alkaline earth metal is used. 0.0 to 50 nm. In addition, when using an alkali halide, the film thickness is preferably as thin as possible from the viewpoint of the ability to inject electrons into the organic layer 3, and is specifically preferably 10 nm or less and more preferably 1 nm or less.

  Moreover, the electron injection layer which consists of a coating film of an organometallic complex is prepared by, for example, applying a coating solution obtained by adding an organometallic complex to a predetermined solvent on the organic layer 3 by a coating method such as a spin coating method. It can be formed by removing. As such organometallic complexes, β-diketonato complexes, quinolinol complexes, and the like can be used. The metal included in the organometallic complex is not particularly limited as long as it has a low work function. For example, alkali metals such as Li, Na, K, and Cs, alkaline earth metals such as Mg, Ca, Sr, and Ba, Includes metals having properties similar to those of alkali metals or alkaline earth metals such as La, Ce, Sn, Zn, and Zr. Further, by further including an electron transporting polymer material or the like in the coating film of the organometallic complex, the electrical properties of the electron injection layer and the adhesion to the organic layer 3 can be further improved. The thickness of the electron injection layer made of the coating film of the organometallic complex is preferably as thin as possible from the viewpoint of the ability to inject electrons into the organic layer 3, and is specifically preferably 10 nm or less and more preferably 1 nm or less.

  The total film thickness of the electron injection layer composed of the coating film of the organometallic complex and the protective electrode layer, that is, the total film thickness of the cathode layer 4 is not particularly limited as long as electron injection into the organic layer 3 is possible. The film thickness of the entire layer 4 is preferably 50 to 500 nm. If the thickness of the protective electrode layer relative to the electron injection layer is too thin, the above effect cannot be obtained sufficiently. If the thickness of the auxiliary electrode is too thick, the stress due to the auxiliary electrode layer increases and dark spots grow. The speed tends to increase.

  In addition, the electron injection layer formed of a metal salt coating film is formed by applying a coating solution obtained by adding a metal salt to a predetermined solvent onto the organic layer 3 by a coating method such as a spin coating method, and removing the solvent from the coating solution. Can be formed. Examples of the metal contained in the metal salt include Ag, Al, Au, Be, Bi, Co, Cu, Fe, Ga, Hg, Ir, Mo, Mn, Nb, Ni, Os, Pb, Pd, Pt, Re, Ru, Sb, Sn, Ti, Zr, etc. are mentioned.

  The metal salt may be either an organic metal salt or an inorganic metal salt. Examples of organometallic salts include substituted or unsubstituted aliphatic carboxylates, divalent carboxylates, aromatic carboxylates, alcoholates, phenolates, dialkylamides, and the like. Examples of the inorganic metal salt include halides.

  The aliphatic carboxylic acid of the aliphatic carboxylate may be either a saturated aliphatic carboxylic acid or an unsaturated aliphatic carboxylic acid. Examples of the saturated aliphatic carboxylate include metal salts such as acetic acid, propionic acid, octanoic acid, isooctanoic acid, decanoic acid, and lauric acid. Examples of the unsaturated aliphatic carboxylate include metal salts such as oleic acid, ricinoleic acid, and linoleic acid.

  Examples of the divalent carboxylate include metal salts of divalent carboxylic acids such as citric acid, malic acid, and oxalic acid.

  Examples of the aromatic carboxylate include benzoic acid, o-tert-butylbenzoic acid, m-tert-butylbenzoic acid, p-tert-butylbenzoic acid, salicylic acid, m-hydroxybenzoic acid, p-hydroxybenzoic acid and the like. Examples of the metal salt include salicylic acid.

  An alcoholate is a metal salt of an alcohol. Examples of the alcohol component constituting the alcoholate include primary alcohols such as ethanol, n-propyl alcohol, and n-butyl alcohol, secondary alcohols such as isopropyl alcohol and isobutyl alcohol, and tertiary alcohols such as tert-butyl alcohol. It is done.

  Phenolate is a metal salt of phenols. The number of hydroxyl groups contained in the phenol component constituting the phenolate is not particularly limited, but is preferably 1 to 2. Such a phenol component may have a substituent (preferably a linear or branched alkyl group having 1 to 8 carbon atoms) in addition to the hydroxyl group. In the present invention, phenol, naphthol, 4-phenylphenol and the like are preferably used.

  Examples of the halide that is an inorganic metal salt include metal salts such as chlorine, fluorine, bromine, and iodine.

  It is preferable to provide an auxiliary electrode layer on these electron injection layers. Thereby, the electron injection efficiency to the organic layer 3 can be improved, and the penetration | invasion of the water | moisture content or the organic solvent to the organic layer 3 or an electron injection layer can be prevented. As a material for the auxiliary electrode layer, a general metal can be used because there is no restriction on work function and charge injection capability. However, it is preferable to use a metal having high conductivity and easy handling. In particular, when the electron injecting layer contains an organic material, it is preferable to select appropriately according to the type and adhesion of the organic material. Specific examples of the material used for the auxiliary electrode layer include Al, Ag, In, Ti, Cu, Au, Mo, W, Pt, Pd, and Ni. Among them, low resistance such as Al and Ag. The use of these metals can further increase the electron injection efficiency. Further, higher sealing properties can be obtained by using a metal compound such as TiN. These materials may be used alone or in combination of two or more. Moreover, when using 2 or more types of metals, you may use as an alloy.

(Spacer and sealing plate)
As shown in FIG. 1, the organic layer 3, further, the anode layer 2 and the cathode layer 4 can be prevented from being deteriorated by sealing the cathode layer 4 side of the organic EL element 9 with the sealing plate 5. . At this time, the spacer 7 is disposed in the non-light emitting region on the insulating layer 6, and the spacer 7 and the sealing plate 5 are adhered to each other, thereby contacting the surface of the organic EL element 9 on the cathode layer 4 side with the sealing plate 5. Can be prevented. The spacer 7 may be an organic material or an inorganic material (including a metal material). Alternatively, the spacer 7 can be formed by a technique such as photolithography using a photosensitive material such as a photoresist or photosensitive polyimide. Further, an adhesive and an insulator such as a glass spacer may be mixed, and the mixture may be applied to the formation region of the spacer 7.

  It is preferable to encapsulate a sealing gas in a space formed by the surface of the organic EL element 9 on the cathode layer 4 side, the sealing plate 5 and the spacer 7. As such a sealing gas, it is preferable to use an inert gas such as Ar or He. The moisture content of the sealing gas is preferably 100 ppm or less, more preferably 10 ppm or less, and even more preferably 1 ppm or less. The lower limit of the moisture content of the sealing gas is not particularly limited, but if it is about 0.1 ppm, the deterioration preventing effect of the organic layer 3, the anode layer 2, the cathode layer 4, and the like is high, which is very preferable.

  According to the said embodiment, the lifetime improvement of an organic EL element can be achieved by making the organic polymer 3 contain the vinyl polymer concerning this invention. Such an organic EL element is very useful in the field of various optical application devices such as an organic EL display, an optical pickup used for memory reading and writing, a relay device provided in an optical communication transmission path, and a photocoupler. is there.

  Next, the organic EL display of the present invention will be described.

  FIG. 2 is a block diagram showing a preferred embodiment of the organic EL display of the present invention. The organic EL display shown in FIG. 2 is a passive drive type, and is a color conversion type organic EL display using a blue light emitting element as an excitation light source. The color conversion method is a method of exciting three color fluorescent elements by visible light emission of high energy rays. In the case of the color conversion method, blue light emission is often generated in the organic layer of the organic EL element, and green light and red light are obtained by exciting the green and red phosphor screens using the blue light emission as excitation light energy rays. Since blue is converted into green and red, it is called a color conversion method.

  In FIG. 2, the display unit 14 includes a substrate 1, an anode layer 2 (first electrode layer) formed on one side of the substrate 1, an organic layer 3 formed on the anode layer 2, and the organic layer 3. A plurality of organic EL elements 9 composed of the formed cathode layer 4 (second electrode layer) are two-dimensionally arranged. Here, in each of the organic EL elements 9, three organic layers 3 containing the vinyl polymer and the blue light emitting dopant according to the present invention corresponding to three light emitting regions (for example, 13a, 13b, 13c). (Light emitting layer) is formed. Of the three light emitting areas, one is a blue light emitting area, and the remaining two are a green light emitting area and a red light emitting area.

  As a material of the substrate 1, for example, a transparent or translucent material such as glass, quartz, or resin is preferable.

  On the substrate 1, as described above, a fluorescence conversion filter film is provided in a region corresponding to two of the three light emitting regions formed in one organic EL element. The emission color is controlled so that a green emission region and a red emission region are obtained. The light emitting region where the fluorescence conversion filter film is not provided is a blue light emitting region.

  The fluorescence conversion filter film absorbs light generated by electroluminescence in the organic layer 3 and emits light of a color different from the absorbed light from the phosphor in the film, and performs color conversion of emission color. Includes a phosphor, a light absorber, and a binder. The fluorescence conversion filter film can be formed by patterning using a technique such as photolithography or printing. In this case, the material for the fluorescence conversion filter film is preferably one that can form fine patterning, and one that is less susceptible to damage in the formation process of the upper layer (the anode layer 2 or the like).

  As the phosphor contained in the fluorescence conversion filter film, one having a high fluorescence quantum yield is preferable, and one having a high light absorption in the emission wavelength region of the light emitting element such as a laser dye is preferable. Examples of such phosphors include rhodamine compounds, perylene compounds, cyanine compounds, phthalocyanine compounds including subphthalo, naphthalimide compounds, condensed ring hydrocarbon compounds, condensed heterocyclic compounds, styryl compounds, and coumarins. System compounds and the like. In addition, when the light absorption property of fluorescent substance itself is inadequate, it is preferable to use a light absorber together, and as this light absorber, what does not quench fluorescence is preferable.

  The binder is not particularly limited as long as it does not quench the fluorescence, and can be appropriately selected from known binders.

  Moreover, it is preferable to combine the constituent material of the organic EL element 9 or a color filter that cuts off short-wavelength external light that can be absorbed by the fluorescence conversion filter film with the fluorescence conversion filter film because the light resistance and display contrast of the element are further improved. .

  In the display unit 14, the two anode layers 2 are formed in parallel with each other on the substrate 1 and the fluorescence conversion filter film so as to pass through the three light emitting regions 13a to 13c of the organic EL element 9, respectively. Has been. Here, the anode layer 2 is disposed so that a part of each of the light emitting regions 13a to 13c is exposed without completely covering the light emitting regions 13a to 13c. The anode layer 2 is a common electrode for a plurality (two in FIG. 2) of organic EL elements, and a power supply unit 8 (described later) is electrically connected to one end of each anode layer 2. Such a striped anode layer 2 can be formed, for example, by forming an ITO film on the substrate 1 on which the fluorescence conversion filter film is patterned, and then performing patterning and etching.

Although not shown in detail, it is preferable to provide an insulator layer such as a SiO ₂ layer or an Al ₂ O ₃ layer on the anode layer 2 after the anode layer 2 is formed. And it is preferable to open the area | region of the insulator layer corresponding to a light emission area | region by an etching etc., and to form the organic layer 3 in this opening part.

  Further, in the display unit 14, the organic layer 3 containing the vinyl polymer according to the present invention and the blue light emitting dopant covers the light emitting region across the anode layer 2 corresponding to each light emitting region of the organic EL element 9. It is formed as follows. Such an organic layer 3 can be suitably formed by a coating method such as a spin coating method.

  Further, in the display unit 14, six cathode layers 4 are formed so as to pass over the organic layer 3 corresponding to the light emitting regions of the organic EL element 9. Each of the cathode layers 4 is a common electrode of a plurality (two in FIG. 2) of organic EL elements, and a switching unit 10 described later is electrically connected to one end of each cathode layer 4.

  In the case of a passive drive type organic EL display as in the present embodiment, it is preferable that the stripe-shaped anode layer 2 and the stripe-shaped cathode layer 4 are arranged so as to be orthogonal to each other as shown in FIG. . At this time, the intersection of the anode layer 2 and the cathode layer 4 in each light emitting region corresponds to one pixel of the display.

  A spacer 7 is provided for each organic EL element 9 in the non-light emitting region of the display unit 14. The surface on the cathode layer 4 side is sealed by adhering a sealing plate (not shown) to the spacer 7.

  In the organic EL display shown in FIG. 2, the drive unit 11 that controls display on the display unit 14 blinks on the organic EL element 9 and the power supply unit 8 that supplies current or voltage to the anode layer 2 and the cathode layer 4. A switching unit 10 for sending a control signal and these control logic circuits 12 are included. The power supply unit 8 is electrically connected to the anode layer 2, and the switching unit 10 is electrically connected to the cathode layer 4, and the power supply unit 8 and the switching unit 10 are electrically connected via the control logic circuit 12. Has been. The driving method of the organic EL element 9 in the display unit 14 is not particularly limited, and for example, DC driving, pulse driving, AC driving, and the like are applicable. In driving, it is preferable to supply a direct current, pulse or alternating current or voltage, and the applied voltage is preferably about 2 to 30V.

  According to the above embodiment, by including the vinyl polymer and the blue light emitting dopant according to the present invention in the organic layer 3, it is possible to obtain blue light emission with high color purity in the light emitting region, and the characteristics are stable over a long period of time. Can be maintained. This blue light emission is extracted from the substrate 1 side as it is in the blue light emission region. Further, in the green light emission region and the red light emission region, green light and red light are emitted from the substrate 1 side by exciting the phosphors corresponding to green and red in the fluorescence conversion filter film using blue light emission as excitation light energy rays, respectively. Taken from. Therefore, according to the present embodiment, an organic EL display having excellent luminance and color display functions and a long life can be realized.

  The organic EL display of the present invention is not limited to the above-described embodiment, and can be determined in consideration of brightness, life, power consumption, cost, and the like necessary for an assumed display product. For example, FIG. 2 shows a so-called passive drive type organic EL display, but the organic EL display of the present invention may be an active drive type full color display using a polysilicon TFT or the like.

  When the organic EL display of the present invention is a full color display, full color display is realized by forming light emitting elements of three primary colors of red, green, and blue (RGB). The full color display method is the same as that in the above embodiment. In addition to the color conversion method shown, any of the RGB three-color juxtaposition method and the white light emission method may be used. The RGB three-color juxtaposition method is a display method in which each of the RGB three-color light emitting elements emits light. The white light emission method is a method of performing full color display by cutting a part of the wavelength of white light emission using a three-color filter used in a liquid crystal display device or the like. In the case of the white light emission method and the color conversion method, it is not necessary to prepare light emitting elements of three colors, the formation of the light emitting elements can be simplified, and an increase in area can be easily handled.

  In the organic EL display of the present invention, any color display method described above can be applied by appropriately selecting a light emitting dopant to be added to the light emitting layer of the organic EL element. For example, the color conversion method can be preferably applied by including a blue light emitting dopant in the organic layer of the organic EL element to form a light emitting layer. In addition, by incorporating a phosphorescent light emitting dopant into the light emitting layer of the organic EL element, the RGB three-color juxtaposition method using phosphorescent light emission can be preferably applied.

  EXAMPLES Hereinafter, although this invention is demonstrated further more concretely based on an Example and a comparative example, this invention is not limited to a following example at all.

Example 1
First, a vinyl polymer having a structural unit represented by the above formula (I-1-1) was synthesized by the procedure described below. Specifically, as represented by the following reaction formula (A-1), 4-bromophenyllithium was added to and reacted with a solution containing anthrone to obtain the target compound. Moreover, as represented by the following reaction formula (B-1), bromine (Br ₂ ) is added to and reacted with a solution containing 9-phenylanthracene, and n-butyllithium is further added and reacted. The desired compound was obtained.

  Next, as represented by the following reaction formula (C-1), the compound obtained by the reaction formula (A-1) and the compound obtained by the reaction formula (B-1) are reacted, To give a compound.

Next, as represented by the following reaction formula (D-1), bromine (Br ₂ ) was added to the solution containing the compound obtained by the reaction formula (C-1) to cause a reaction. The bromide was purified by column chromatography. Then, the obtained bromide was dissolved in a predetermined solvent and reacted by adding 4-vinylphenylboronic acid and a predetermined catalyst to obtain the target compound. Furthermore, a benzoyl peroxide (BPO) as a radical polymerization initiator is added to the solution containing the obtained compound so that the content becomes 1 wt%, and a polymerization reaction is performed. By the above formula (I-1-1) Vinyl polymers having the structural units represented were synthesized.

  Next, a 2.0 wt% toluene solution of this vinyl polymer was prepared, and tetraphenylbutadiene was added as a dopant in a proportion of 2 wt% with respect to the monomer unit in the vinyl polymer to obtain a light emitting layer coating solution. Using this solution, an organic EL device was produced by the following procedure.

  A coating solution containing polyethylene dioxythiophene / polystyrene sulfonic acid (PEDOT / PSS) is applied onto an ITO substrate by spin coating, and dried in nitrogen at 180 ° C. for 5 minutes to form a film with a thickness of 50 nm. A hole transport layer was formed. Thereafter, the above light emitting layer coating solution was applied onto the hole transport layer and vacuum dried at 180 ° C. for 1 hour to form a light emitting layer having a thickness of 100 nm. Furthermore, vacuum deposition was performed in this order so that the LiF film thickness was 0.6 nm and the Al film thickness was 250 nm, and the cathode side surface was sealed to obtain the target organic EL device.

In the obtained organic EL element, blue light emission derived from tetraphenylbutadiene was obtained. Further, the current efficiency of the obtained organic EL element was 3.5 cd / A when driven at a constant current of 10 mA / cm ² . Further, when the luminance half-life test was performed by driving at a constant current of 10 mA / cm ² , the luminance half-life was 920 hours.

(Example 2)
First, a vinyl polymer having a structural unit represented by the above formula (I-1-2) was synthesized by the procedure described below. Specifically, the target compound was obtained as represented by the above reaction formula (A-1). Moreover, as represented by the following reaction formula (B-2), bromine (Br ₂ ) is added to the solution containing 9-biphenyl-2-yl-anthracene and reacted, and then n-butyllithium is added. To give the desired compound.

  Next, as represented by the following reaction formula (C-2), the compound obtained by the reaction formula (A-1) and the compound obtained by the reaction formula (B-2) are reacted, To give a compound.

Next, as represented by the following reaction formula (D-2), bromine (Br ₂ ) was added to the solution containing the compound obtained by the reaction formula (C-2) to cause a reaction. The bromide was purified by column chromatography. Then, the obtained bromide was dissolved in a predetermined solvent and reacted by adding 4-vinylphenylboronic acid and a predetermined catalyst to obtain the target compound. Further, a benzoyl peroxide (BPO) as a radical polymerization initiator is added to the solution containing the obtained compound so that the content becomes 1 wt%, and a polymerization reaction is performed, and the above formula (I-1-2) Vinyl polymers having the structural units represented were synthesized.

  Next, a light emitting layer forming coating solution was prepared in the same manner as in Example 1 except that the obtained vinyl polymer was used. Furthermore, an organic EL device was produced in the same manner as in Example 1 except that the light emitting layer forming coating solution was used.

In the obtained organic EL element, blue light emission derived from tetraphenylbutadiene was obtained. Moreover, the current efficiency of the obtained organic EL element was 3.8 cd / A when driven at a constant current of 10 mA / cm ² . Further, when the luminance half-life test was performed by driving at a constant current of 10 mA / cm ² , the luminance half-life was 1100 hours.

(Comparative Example 1)
First, a vinyl polymer having a target structural unit in which two anthracene skeletons are bonded by a single bond instead of a phenylene group in the structural unit represented by the above formula (I-1-1) by the procedure described below. Synthesized. Specifically, as represented by the following reaction formula (A-3), bromine (Br ₂ ) was added to and reacted with a solution containing 9-phenylanthracene. Next, n-butyllithium was added, and anthrone was further added and reacted to obtain the target compound.

  Next, as represented by the reaction formula (C-3), pure water is added to the solution containing the compound obtained by the reaction formula (A-3), the solvent is removed from the reaction solution after the reaction, and the residue The product was dissolved in a predetermined solvent and then dehydrated to obtain the target compound.

Next, as represented by the following reaction formula (D-3), bromine (Br ₂ ) was added to the solution containing the compound obtained by the reaction formula (C-3) and allowed to react. The bromide was purified by column chromatography. Then, the obtained bromide was dissolved in a predetermined solvent and reacted by adding 4-vinylphenylboronic acid and a predetermined catalyst to obtain the target compound. Further, a benzoyl peroxide (BPO) as a radical polymerization initiator is added to the solution containing the obtained compound so as to have a content of 1 wt%, a polymerization reaction is performed, and a vinyl polymer having a target structural unit is obtained. Synthesized.

  Next, a light emitting layer forming coating solution was prepared in the same manner as in Example 1 except that the obtained vinyl polymer was used. Furthermore, an organic EL device was produced in the same manner as in Example 1 except that the light emitting layer forming coating solution was used.

In the obtained organic EL element, blue light emission derived from tetraphenylbutadiene was obtained. Further, the current efficiency of the obtained organic EL element was 3.2 cd / A when driven at a constant current of 10 mA / cm ² . Furthermore, when the luminance half-life test was performed by driving at a constant current of 10 mA / cm ² , the luminance half-life was 600 hours.

(Comparative Example 2)
First, a vinyl polymer having a target structural unit having no phenylene group and one anthracene skeleton in the structural unit represented by the formula (I-1-2) was synthesized by the procedure described below. Specifically, as represented by the following reaction formula (A-4), biphenyl lithium was added to and reacted with a solution containing anthrone to obtain the target compound.

Next, as represented by the following reaction formula (D-4), bromine (Br ₂ ) was added to the solution containing the compound obtained by the reaction formula (A-4) and allowed to react. The bromide was purified by column chromatography. Then, the obtained bromide was dissolved in a predetermined solvent and reacted by adding 4-vinylphenylboronic acid and a predetermined catalyst to obtain the target compound. Further, a benzoyl peroxide (BPO) as a radical polymerization initiator is added to the solution containing the obtained compound so as to have a content of 1 wt%, a polymerization reaction is performed, and a vinyl polymer having a target structural unit is obtained. Synthesized.

  Next, a light emitting layer forming coating solution was prepared in the same manner as in Example 1 except that the obtained vinyl polymer was used. Furthermore, an organic EL device was produced in the same manner as in Example 1 except that the light emitting layer forming coating solution was used.

In the obtained organic EL element, blue light emission derived from tetraphenylbutadiene was obtained. Further, the current efficiency of the obtained organic EL element was 4.0 cd / A when driven at a constant current of 10 mA / cm ² . Further, when the luminance half-life test was performed by driving at a constant current of 10 mA / cm ² , the luminance half-life was 580 hours.

(Comparative Example 3)
First, a vinyl polymer having a target structural unit in which two anthracene skeletons are bonded to each other by an anthracenylene group instead of a phenylene group in the structural unit represented by the above formula (I-1-1) by the procedure described below. Synthesized. Specifically, the target compound was obtained from 9-bromoanthracene as represented by the following reaction formula (A-5). Moreover, the target compound was obtained as represented by the above reaction formula (B-1).

  Next, as represented by the reaction formula (C-5), the compound obtained by the reaction formula (A-5) and the compound obtained by the reaction formula (B-1) are reacted, and the target A compound was obtained.

Next, as represented by the following reaction formula (D-5), bromine (Br ₂ ) was added to the solution containing the compound obtained by the reaction formula (C-5) to cause a reaction. The bromide was purified by column chromatography. Then, the obtained bromide was dissolved in a predetermined solvent and reacted by adding 4-vinylphenylboronic acid and a predetermined catalyst to obtain the target compound. Further, a benzoyl peroxide (BPO) as a radical polymerization initiator is added to the solution containing the obtained compound so as to have a content of 1 wt%, a polymerization reaction is performed, and a vinyl polymer having a target structural unit is obtained. Synthesized.

  Next, a light emitting layer forming coating solution was prepared in the same manner as in Example 1 except that the obtained vinyl polymer was used. Furthermore, an organic EL device was produced in the same manner as in Example 1 except that the light emitting layer forming coating solution was used.

In the obtained organic EL element, blue light emission derived from tetraphenylbutadiene was obtained. Further, the current efficiency of the obtained organic EL element was 2.3 cd / A when driven at a constant current of 10 mA / cm ² . Further, when the luminance half-life test was performed by driving at a constant current of 10 mA / cm ² , the luminance half-life was 300 hours. In the organic EL device of Comparative Example 3, the light emitting layer was crystallized so that the film state was unstable.

It is a schematic cross section which shows suitable one Embodiment of the organic EL element of this invention. It is a block diagram which shows suitable one Embodiment of the organic electroluminescent display of this invention.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 ... Board | substrate, 2 ... Anode layer (1st electrode layer), 3 ... Organic layer, 4 ... Cathode layer (2nd electrode layer), 5 ... Sealing plate, 6 ... Insulator layer, 7 ... Spacer, 8 DESCRIPTION OF SYMBOLS ... Power supply part, 9 ... Organic EL element, 10 ... Switching part, 11 ... Drive part, 12 ... Control logic circuit, 13 ... Light emission area | region, 14 ... Display part.

Claims (5)

A pair of electrodes disposed opposite each other;
An organic layer containing a vinyl polymer disposed between the electrodes and having a structural unit represented by the following formula (I):
An organic EL device comprising:

[In formula (I), X represents a divalent organic group, L represents a (p + 2) valent aromatic group having 6 to 13 carbon atoms , and Y, R ¹ and R ² are each independently a monovalent group. A represents a substituent, a represents an integer of 0 to 8, b represents an integer of 0 to 9, p represents 0 or an integer of 1 or more, and n represents an integer of 1 or more. ]   2. The organic EL device according to claim 1, wherein the aromatic group represented by L is a phenylene group, a naphthylene group, a biphenylylene group, a fluorenylene group, or a carbazolylene group. The organic EL device according to claim 1, wherein the structural unit represented by the formula (I) is a structural unit represented by the following formula (I-1).

[In Formula (I-1), X represents a divalent organic group, L represents a (p + 2) -valent aromatic group having 6 to 13 carbon atoms , and Y, R ¹ , R ³ and R ⁴ are each Independently represents a monovalent substituent, a represents an integer of 0 to 8, c represents an integer of 1 to 9, p represents 0 or an integer of 1 or more, and n represents an integer of 1 or more. ]   The organic EL element according to claim 1, wherein the organic layer further contains a light-emitting dopant. A plurality of organic EL elements each having a pair of electrodes disposed opposite to each other and an organic layer containing a vinyl polymer having a structural unit represented by the following formula (I) disposed between the electrodes are arranged. Display,
A power supply unit that is electrically connected to each of the pair of electrodes and supplies a voltage or current to the electrodes; and a switching unit that turns on or off each of the organic EL elements;
An organic EL display comprising:

[In formula (I), X represents a divalent organic group, L represents a (p + 2) valent aromatic group having 6 to 13 carbon atoms , and Y, R ¹ and R ² are each independently a monovalent group. A represents a substituent, a represents an integer of 0 to 8, b represents an integer of 0 to 9, p represents 0 or an integer of 1 or more, and n represents an integer of 1 or more. ]

Images