JP6769020B2 - Charge transporting material, ink composition using the material, organic electronics element, organic electroluminescence element, display element, lighting device, and display device. - Google Patents

Description

An embodiment of the present invention relates to a charge transporting material and an ink composition using the material. Further, another embodiment of the present invention relates to an organic electronic device, an organic electroluminescence device, a display device, a lighting device, and a display device having an organic layer using the charge transporting material or the ink composition. ..

Organic electronics devices are devices that perform electrical operations using organic substances, and are expected to exhibit features such as energy saving, low cost, and flexibility, and are attracting attention as a technology that replaces conventional silicon-based inorganic semiconductors. ing.

Examples of organic electronics devices include organic electroluminescence devices (hereinafter, also referred to as “organic EL devices”), organic photoelectric conversion devices, and organic transistors.

Among organic electronic devices, organic EL devices are attracting attention as large-area solid-state light source applications as alternatives to incandescent lamps and gas-filled lamps, for example. It is also attracting attention as the most promising self-luminous display that can replace the liquid crystal display (LCD) in the flat panel display (FPD) field, and its commercialization is progressing.

Organic EL devices are roughly classified into two types, low molecular weight organic EL devices and high molecular weight organic EL devices, according to the organic materials used. In the polymer-type organic EL element, a polymer material is used as the organic material, and in the low-molecular-weight organic EL element, a low-molecular-weight material is used. Compared to low-molecular-weight organic EL devices, which are mainly formed in a vacuum system, high-molecular-weight organic EL devices can be easily formed by wet processes such as printing and inkjet. It is expected as an indispensable element for EL displays.

Therefore, the development of a material suitable for a wet process is underway, and for example, studies as described in Patent Document 1 are being conducted.

Japanese Unexamined Patent Publication No. 2006-279007

In general, an organic EL device manufactured by a wet process using a polymer material has features that it is easy to reduce the cost and increase the area. However, an organic EL device containing a thin film produced by using a conventional polymer material is desired to be further improved in the characteristics of the organic EL device such as driving voltage, luminous efficiency, and luminous life.

In view of the above, one embodiment of the present invention aims to provide a charge-transporting material containing a charge-transporting polymer that can be used for an organic electronic device, and an ink composition containing the material. Further, in another embodiment, an organic electronic device and an organic EL device having excellent luminous efficiency and light emitting life by using the charge transporting material or the ink composition, and a display element and a lighting device using the same are used. , And a display device is intended to be provided.

As a result of diligent studies, the present inventors have found that a charge-transporting polymer having a specific structural unit is suitable as a charge-transporting material constituting an organic layer of an organic electronic device, and complete the present invention. I arrived.

One embodiment of the present invention relates to a charge transporting material comprising a charge transporting polymer comprising at least one of a divalent structural unit L1 having a triazine ring and a trivalent or higher valent structural unit B1 having a triazine ring.
Here, the charge-transporting polymer has a divalent structural unit L2 having a charge-transporting property and a charge other than the divalent structural unit L1 having the triazine ring and the trivalent or higher-valent structural unit B1 having the triazine ring. It is preferable to further contain at least one of the trivalent or higher valent structural unit B2 having transportability. It is more preferable that the charge-transporting polymer further contains a divalent structural unit L2 having a charge-transporting property other than the divalent structural unit L1 having a triazine ring. The divalent structural unit L2 having charge transportability preferably contains a structure selected from the group consisting of an aromatic amine structure, a carbazole structure, a thiophene structure, a bithiophene structure, a benzene structure, and a fluorene structure. The charge-transporting polymer preferably has a structure branched in three or more directions. The charge transporting material is preferably used as a hole transporting material.
One embodiment of the present invention relates to an ink composition containing the charge transporting material of the above embodiment and a solvent.
One embodiment of the present invention relates to an organic electronic device having an organic layer containing the charge transporting material of the above embodiment.
One embodiment of the present invention relates to an organic electroluminescent device having an organic layer containing the charge transporting material of the above embodiment. Here, the organic electroluminescence element preferably further has a flexible substrate, and the flexible substrate preferably contains a resin film.
One embodiment of the present invention relates to a display device including the organic electroluminescence device of the above embodiment.
One embodiment of the present invention relates to a lighting device including the organic electroluminescence device of the above embodiment.
One embodiment of the present invention relates to a display device including the lighting device of the above embodiment and a liquid crystal element as a display means.

According to the embodiment of the present invention, an organic electronics element, an organic EL element, and a display element, a lighting device, and a display device using the organic electronics element, the organic EL element, which are excellent in durability, low drive voltage, luminous efficiency, and emission life. Can be provided.

It is a schematic cross-sectional view which shows one Embodiment of the organic EL element of this invention.

Hereinafter, embodiments of the present invention will be described.
<Charge transport material>
The charge transport material according to the present invention includes a charge transport polymer containing a structural unit having a triazine ring. The charge-transporting polymer has the ability to transport charges. Hereinafter, the charge transporting polymer will be described in detail.

(Charge transport polymer)
In the present invention, the charge-transporting polymer may contain a structural unit having a triazine ring in the molecule and exhibits charge-transporting property. The structural unit having a triazine ring may contain three isomers having different nitrogen positions. In one embodiment, the structural unit having a triazine ring includes the structure of the 1,3,5-triazine ring shown in the following formula.

The charge-transporting polymer containing the structural unit having a triazine ring may have a linear structure or a branched structure. The charge-transporting polymer preferably contains at least a divalent structural unit L having charge transportability and a monovalent structural unit T constituting the terminal portion, and further comprises a trivalent or higher-valent structural unit constituting the branch portion. B may be included. The charge-transporting polymer may contain only one type of each structural unit, or may contain a plurality of types of each structural unit. In charge-transporting polymers, the structural units are attached to each other at "monovalent" to "trivalent or higher" binding sites.

(Construction)
Examples of the partial structure contained in the charge transport polymer include the following. The charge-transporting polymer is not limited to those having the following partial structures. In the partial structure, "L" represents the structural unit L, "T" represents the structural unit T, and "B" represents the structural unit B. "*" Represents a binding site with another structural unit. In the following substructures, the plurality of Ls may be the same structural unit or different structural units from each other. The same applies to T and B.

Linear charge transport polymer

Charge-transporting polymer with branched structure

In one embodiment, the charge transport polymer comprises at least one of a divalent structural unit L1 having a triazine ring and a trivalent or higher valent structural unit B1 having a triazine ring. Specifically, it is as follows.

(Structural unit L1)
The structural unit L1 is intended to have two binding sites with other structural units as a whole, and preferably has a structure in which an arylene group or an alletriyl group is bonded to the triazine ring. Examples of the divalent structural unit L1 having a triazine ring include the following.

Here, in the formula, R is an independently hydrogen atom or a linear, cyclic or branched alkyl group, alkenyl group, alkynyl group, and alkoxy group having 1 to 22 carbon atoms. , And at least one selected from the group consisting of aryl groups and heteroaryl groups having 2 to 30 carbon atoms. The aryl group and heteroaryl group may have a substituent. R is preferably a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, more preferably a substituted or unsubstituted aryl group having 6 to 20 carbon atoms, and a substituted or unsubstituted phenyl group or naphthyl group. Is even more preferable.
In the formula, Ar is a substituted or unsubstituted arylene group or allenetriyl group having 6 to 30 carbon atoms, and preferably a substituted or unsubstituted arylene group having 6 to 20 carbon atoms. The arylene group is preferably a phenylene group or a naphthylene group, and more preferably a phenylene group. The phenylene group may be any of 1,2-phenylene group, 1,3-phenylene group and 1,4-phenylene group, but 1,4-phenylene group is preferable. In the formula, "*" represents a binding site with another structural unit.

Specific examples of the structural unit L1 include the following. However, the structural unit L1 is not limited to the following.

(Structural unit B1)
The structural unit B1 is intended to have a triazine ring and, as a whole, to have three or more binding sites with other structural units. From the viewpoint of improving the durability of the organic electronic device, the structural unit B1 is preferably hexavalent or less, and more preferably trivalent or tetravalent. The structural unit B1 preferably has a structure in which an arylene group or an arenetriyl group is bonded to a triazine ring.

Examples of the trivalent or higher valent structural unit B1 having a triazine ring include the following.

In the formula, Ar represents a substituted or unsubstituted arylene group or arenetriyl group having 6 to 30 carbon atoms, and a structural unit in which Ar is an arylene group is preferable. More preferably, it is a substituted or unsubstituted arylene group having 6 to 20 carbon atoms. The arylene group is preferably a substituted or unsubstituted phenylene group or a naphthylene group, and more preferably an unsubstituted phenylene group. The phenylene group may be any of 1,2-phenylene group, 1,3-phenylene group and 1,4-phenylene group, but 1,4-phenylene group is preferable. In the formula, "*" represents a binding site with another structural unit.

Specific examples of the structural unit B1 include the following. However, the structural unit B1 is not limited to the following.

Specific examples of the preferable structural unit L1 and the structural unit B1 are as follows.

In one embodiment, the charge-transporting polymer further comprises a charge-transporting divalent structural unit L2 and a charge-transporting trivalent or higher structural unit B2 other than the structural unit L1 and the structural unit B1. It is preferable to include at least one. Specifically, it is as follows.
(Structural unit L2)
The structural unit L2 is a divalent structural unit having charge transportability. The structural unit L2 may include an atomic group capable of transporting electric charges, and is not particularly limited. For example, the structural unit L2 is a substituted or unsubstituted aromatic amine structure, carbazole structure, thiophene structure, fluorene structure, benzene structure, biphenylene structure, turphenylene structure, naphthalene structure, anthracene structure, tetracene structure, phenanthrene structure, dihydro. Phenanthrene structure, pyridine structure, pyrazine structure, quinoline structure, isoquinoline structure, quinoxalin structure, aclysine structure, diazaphenanthrene structure, furan structure, pyrrole structure, oxazole structure, oxaziazole structure, thiazole structure, thiazazole structure, triazole structure, benzo It is selected from a thiophene structure, a benzoxazole structure, a benzoxaziazole structure, a benzothiazole structure, a benzothiazazole structure, a benzotriazole structure, and a structure containing one or more of these. The aromatic amine structure is preferably a triarylamine structure, more preferably a triphenylamine structure.

In one embodiment, the structural unit L2 is a substituted or unsubstituted aromatic amine structure, carbazole structure, thiophene structure, fluorene structure, benzene structure, pyrrole structure, and these, from the viewpoint of obtaining excellent hole transportability. It is preferable to select from a structure containing one or more of these, and to be selected from a substituted or unsubstituted aromatic amine structure, a carbazole structure, and a structure containing one or more of these. Is more preferable. In other embodiments, the structural unit L2 is substituted or unsubstituted, fluorene structure, benzene structure, phenanthrene structure, pyridine structure, quinoline structure, and one or two of them, from the viewpoint of obtaining excellent electron transportability. It is preferably selected from structures containing more than a species.

Specific examples of the structural unit L2 include the following. However, the structural unit L2 is not limited to the following.

R each independently represents a hydrogen atom or a substituent. Preferably, R independently comprises -R ¹ , -OR ² , -SR ³ , -OCOR ⁴ , -COOR ⁵ , -SiR ⁶ R ⁷ R ⁸ , a halogen atom, and a polymerizable functional group described below. Selected from the group of groups containing. R ^{1 to} R ⁸ independently represent a hydrogen atom; a linear, cyclic or branched alkyl group having 1 to 22 carbon atoms; or an aryl group or a heteroaryl group having 2 to 30 carbon atoms. An aryl group is an atomic group obtained by removing one hydrogen atom from an aromatic hydrocarbon. A heteroaryl group is an atomic group obtained by removing one hydrogen atom from an aromatic heterocycle. The alkyl group may be further substituted with an aryl group or a heteroaryl group having 2 to 20 carbon atoms, and the aryl group or a heteroaryl group may be further substituted with a linear, cyclic or branched having 1 to 22 carbon atoms. It may be substituted with an alkyl group. R is preferably a hydrogen atom, an alkyl group, an aryl group, or an alkyl-substituted aryl group. Ar represents an arylene group or a heteroarylene group having 2 to 30 carbon atoms. Ar is preferably an arylene group, more preferably a phenylene group. A heteroarylene group is an atomic group obtained by removing two hydrogen atoms from an aromatic heterocycle. Ar is preferably an arylene group, more preferably a phenylene group.

Examples of the aromatic hydrocarbon include a monocyclic ring, a condensed ring, and a polycyclic ring in which two or more selected from a monocyclic ring and a condensed ring are bonded via a single bond. Examples of the aromatic heterocycle include a monocyclic ring, a condensed ring, and a polycyclic ring in which two or more selected from a monocyclic ring and a condensed ring are bonded via a single bond.

(Structural unit B2)
The structural unit B2 is a trivalent or higher structural unit constituting the branched portion when the charge-transporting polymer has a branched structure. The structural unit B2 is preferably hexavalent or less, and more preferably trivalent or tetravalent, from the viewpoint of improving the durability of the organic electronic device. The structural unit B2 is preferably a unit having charge transportability. For example, the structural unit B2 is a substituted or unsubstituted aromatic amine structure, carbazole structure, condensed polycyclic aromatic hydrocarbon structure, and one or two of them from the viewpoint of improving the durability of the organic electronic device. Selected from structures containing more than a species. The aromatic amine structure is preferably a triarylamine structure, more preferably a triphenylamine structure. The structural unit B2 may have the same structure as the structural unit L2, or may have a different structure.

Specific examples of the structural unit B2 include the following. However, the structural unit B2 is not limited to the following.

W represents a trivalent linking group, for example, an allene triyl group having 2 to 30 carbon atoms or a hetero allene triyl group (excluding a group containing a triazine ring). The arenetriyl group is an atomic group obtained by removing three hydrogen atoms from an aromatic hydrocarbon. A heteroarene triyl group is an atomic group obtained by removing three hydrogen atoms from an aromatic heterocycle. Ar independently represents a divalent linking group, for example, each independently represents an arylene group or a heteroarylene group having 2 to 30 carbon atoms. Ar is preferably an arylene group, more preferably a phenylene group. Y represents a divalent linking group, for example, from a group having one or more hydrogen atoms in R (excluding a group containing a polymerizable functional group) in the structural unit L2, one more hydrogen atom. Divalent groups excluding. Z represents either a carbon atom, a silicon atom, or a phosphorus atom. In the structural unit, the benzene ring and Ar may have a substituent, and examples of the substituent include R in the structural unit L2.

(Structural unit T)
In the charge-transporting polymer, the structural unit T is a monovalent structural unit constituting the terminal portion of the charge-transporting polymer. The structural unit T is not particularly limited, and is selected from, for example, a substituted or unsubstituted aromatic hydrocarbon structure, an aromatic heterocyclic structure, and a structure containing one or more of these. In one embodiment, the structural unit T is preferably a substituted or unsubstituted aromatic hydrocarbon structure from the viewpoint of imparting durability without reducing charge transportability, and is preferably a substituted or unsubstituted benzene. The structure is more preferable. Further, in another embodiment, as described later, when the charge-transporting polymer has a polymerizable functional group at the terminal portion, the structural unit T has a polymerizable structure (that is, for example, a polymerizable structure such as a pyrrole-yl group). It may be a functional group). The structural unit T may have the same structure as the structural units L2 and / or B2, or may have a different structure.

Specific examples of the structural unit T include the following. However, the structural unit T is not limited to the following.

R is the same as R in the structural unit L2. When the charge-transporting polymer has a polymerizable functional group at the terminal portion, preferably at least one of R is a group containing a polymerizable functional group.

In one embodiment, the charge transport polymer has at least one of a divalent structural unit L1 having a triazine ring and a trivalent or higher structural unit B1 having a triazine ring, and further having the triazine ring. And, other than the structural unit B1, it is preferable to include a divalent structural unit L2 having charge transportability. Here, the divalent structural unit L2 is preferably a structure selected from the group consisting of an aromatic amine structure, a carbazole structure, a thiophene structure, a bithiophene structure, a benzene structure, and a fluorene structure. The aromatic amine structure is preferably a triarylamine structure, more preferably a triphenylamine structure. The benzene structure is preferably a p-phenylene structure or an m-phenylene structure. In one embodiment, the divalent structural unit L2 is more preferably a triphenylamine structure or a carbazole structure.

In one embodiment, the charge-transporting polymer preferably contains trivalent or higher structural units B1 and / or B2 and has a structure branched in three or more directions. In such an embodiment, the charge transport polymer preferably contains at least trivalent or higher structural unit B1. The "structure branched in three or more directions" means that the degree of polymerization is the same as that of the main chain when the chain having the highest degree of polymerization is used as the main chain among various chains in one molecule of the charge-transporting polymer. Or, it means that there is one or more side chains having a smaller degree of polymerization. In the present invention, the degree of polymerization indicates how many units of the monomer used in synthesizing the charge-transporting polymer are contained in one molecule of the charge-transporting polymer. In the present invention, the side chain is a chain different from the main chain of the charge-transporting polymer and has at least one structural unit, and the other chains are regarded as substituents rather than side chains.

(Polymerizable functional group)
In one embodiment, the charge-transporting polymer preferably has at least one polymerizable functional group from the viewpoint of curing by a polymerization reaction and changing the solubility in a solvent. The "polymerizable functional group" refers to a functional group capable of forming a bond with each other by applying heat and / or light.

The polymerizable functional group includes a group having a carbon-carbon multiple bond (for example, vinyl group, allyl group, butenyl group, ethynyl group, acryloyl group, acryloyloxy group, acryloylamino group, methacryloyl group, methacryloyloxy group, methacryloylamino). Group, vinyloxy group, vinylamino group, etc.), group having a small ring (for example, cyclic alkyl group such as cyclopropyl group, cyclobutyl group; cyclic ether group such as epoxy group (oxylanyl group), oxetan group (oxetanyl group)) Examples include a diketen group; an episulfide group; a lactone group; a lactam group, etc.), a heterocyclic group (for example, a furan-yl group, a pyrrole-yl group, a thiophen-yl group, a silol-yl group) and the like. As the polymerizable functional group, a vinyl group, an acryloyl group, a methacryloyl group, an epoxy group, and an oxetane group are particularly preferable, and a vinyl group, an oxetan group, or an epoxy group is more preferable from the viewpoint of reactivity and characteristics of the organic electronic device. preferable.

From the viewpoint of increasing the degree of freedom of the polymerizable functional group and facilitating the occurrence of a polymerization reaction, it is preferable that the main skeleton of the charge-transporting polymer and the polymerizable functional group are linked by an alkylene chain. Further, for example, when an organic layer is formed on an electrode, it may be connected by a hydrophilic chain such as an ethylene glycol chain or a diethylene glycol chain from the viewpoint of improving the affinity with a hydrophilic electrode such as ITO. preferable. Further, from the viewpoint of facilitating the preparation of the monomer used for introducing the polymerizable functional group, the charge transport polymer polymerizes with the terminal portion of the alkylene chain and / or the hydrophilic chain, that is, these chains. The linking portion with the sex functional group and / or the connecting portion between these chains and the skeleton of the charge-transporting polymer may have an ether bond or an ester bond. The above-mentioned "group containing a polymerizable functional group" means a polymerizable functional group itself or a group in which a polymerizable functional group and an alkylene chain are combined. As the group containing a polymerizable functional group, for example, the group exemplified in International Publication No. WO2010 / 1405553 can be preferably used.

The polymerizable functional group is introduced at the terminal portion (that is, the structural unit T) of the charge-transporting polymer or at a portion other than the terminal portion (that is, the structural unit L or B). It may be introduced in both the and non-terminal parts. From the viewpoint of curability, it is preferable that it is introduced at least at the terminal portion, and from the viewpoint of achieving both curability and charge transportability, it is preferable that it is introduced only at the terminal portion. Further, when the charge-transporting polymer has a branched structure, the polymerizable functional group may be introduced into the main chain or the side chain of the charge-transporting polymer, and both the main chain and the side chain may be introduced. It may be introduced in.

From the viewpoint of contributing to the change in solubility, the polymerizable functional group is preferably contained in a large amount in the charge-transporting polymer. On the other hand, from the viewpoint of not hindering the charge transportability, it is preferable that the amount contained in the charge transport polymer is small. The content of the polymerizable functional group can be appropriately set in consideration of these.

For example, the number of polymerizable functional groups per molecule of the charge-transporting polymer is preferably 2 or more, and more preferably 3 or more, from the viewpoint of obtaining a sufficient change in solubility. The number of polymerizable functional groups is preferably 1,000 or less, more preferably 500 or less, from the viewpoint of maintaining charge transportability.

The number of polymerizable functional groups per molecule of the charge-transporting polymer is the amount of the polymerizable functional group charged (for example, the amount of the monomer having the polymerizable functional group) used for synthesizing the charge-transporting polymer, and each structure. It can be obtained as an average value by using the amount of monomer charged corresponding to the unit, the weight average molecular weight of the charge-transporting polymer, and the like. The number of polymerizable functional groups is the ratio of the integrated value of the signal derived from the polymerizable functional group in the ¹ H NMR (nuclear magnetic resonance) spectrum of the charge transport polymer to the integrated value of the entire spectrum, and the charge transport polymer. It can be calculated as an average value by using the weight average molecular weight of. Since it is simple, when the amount to be charged is clear, the value obtained by using the amount to be charged is preferably adopted.

(Number average molecular weight)
The number average molecular weight of the charge-transporting polymer can be appropriately adjusted in consideration of solubility in a solvent, film-forming property, and the like. The number average molecular weight is preferably 500 or more, more preferably 1,000 or more, and even more preferably 2,000 or more, from the viewpoint of excellent charge transportability. The number average molecular weight is preferably 1,000,000 or less, more preferably 100,000 or less, and more preferably 50,000 or less, from the viewpoint of maintaining good solubility in a solvent and facilitating the preparation of the ink composition. The following is more preferable.

(Weight average molecular weight)
The weight average molecular weight of the charge-transporting polymer can be appropriately adjusted in consideration of solubility in a solvent, film-forming property, and the like. The weight average molecular weight is preferably 1,000 or more, more preferably 5,000 or more, still more preferably 10,000 or more, from the viewpoint of excellent charge transportability. The weight average molecular weight is preferably 1,000,000 or less, more preferably 700,000 or less, and more preferably 400,000 or less, from the viewpoint of maintaining good solubility in the solvent and facilitating the preparation of the ink composition. The following is more preferable.

The number average molecular weight and the weight average molecular weight can be measured by gel permeation chromatography (GPC) using a standard polystyrene calibration curve.

(Ratio of structural units)
The ratio of the structural unit having a triazine ring contained in the charge transport polymer, that is, the ratio of the structural unit L1 and / or the structural unit B1 with respect to all the structural units is 1 mol from the viewpoint of obtaining excellent durability. % Or more is preferable, 3 mol% or more is more preferable, and 5 mol% or more is most preferable. On the other hand, from the viewpoint of further enhancing the charge transportability of the charge transport polymer, the charge transport polymer preferably further contains a structural unit having charge transportability other than the structural unit L1 and / or the structural unit B1. From such a viewpoint, in one embodiment, the ratio of the structural unit L1 and / or the structural unit B1 is preferably 90 mol% or less, more preferably 80 mol% or less, and 70 mol% or less based on all the structural units. Is more preferable. In one embodiment, the proportion of structural units having a triazine ring in the charge transport polymer is preferably 1 to 90 mol%, more preferably 3 to 80 mol%, still more preferably 5 to 5 based on all structural units. It is in the range of 70 mol%. The above ratio is also preferable in that a charge-transporting polymer having an appropriate molecular weight can be obtained as a charge-transporting material.

In the charge transporting polymer, the ratio of the divalent structural unit L is preferably 10 mol% or more, more preferably 20 mol% or more, and more preferably 30 mol, based on all the structural units, from the viewpoint of obtaining sufficient charge transportability. % Or more is more preferable. Further, the ratio of the structural unit L is preferably 95 mol% or less, more preferably 90 mol% or less, still more preferably 85 mol% or less, considering the structural unit T and the structural unit B to be introduced as needed. Here, the structural unit L means the sum of the structural unit L1 and the structural unit L2 introduced as needed. From the viewpoint of expressing the effect of the structural unit having a triazine ring, the ratio of the structural unit L1 to the total amount of L1 and L2 is preferably 1 mol% or more, more preferably 3 mol% or more, still more preferably 5 mol% or more. Is.

The ratio of the structural unit T contained in the charge-transporting polymer is based on all the structural units from the viewpoint of improving the characteristics of the organic electronic device or from the viewpoint of suppressing the increase in viscosity and satisfactorily synthesizing the charge-transporting polymer. 5 mol% or more is preferable, 10 mol% or more is more preferable, and 15 mol% or more is further preferable. The ratio of the structural unit T is preferably 60 mol% or less, more preferably 55 mol% or less, still more preferably 50 mol% or less, from the viewpoint of obtaining sufficient charge transportability.

When the charge transport polymer contains a structural unit B having a valence of 3 or more, the ratio of the structural unit B is preferably 1 mol% or more, preferably 5 mol, based on all the structural units, from the viewpoint of improving the durability of the organic electronic device. % Or more is more preferable, and 10 mol% or more is further preferable. The ratio of the structural unit B is preferably 50 mol% or less, preferably 40 mol% or less, from the viewpoint of suppressing an increase in viscosity and satisfactorily synthesizing a charge-transporting polymer, or obtaining sufficient charge-transporting property. Is more preferable, and 30 mol% or less is further preferable. Here, the structural unit B means the total of the structural unit B1 and the structural unit B2 introduced as needed. From the viewpoint of expressing the effect of the structural unit having a triazine ring, the ratio of the structural unit B1 to the total amount of B1 and B2 is preferably 1 mol% or more, more preferably 3 mol% or more, still more preferably 5 mol% or more. Is.

When the charge-transporting polymer has a polymerizable functional group, the ratio of the polymerizable functional group is preferably 0.1 mol% or more based on all structural units from the viewpoint of efficiently curing the charge-transporting polymer. 1 mol% or more is more preferable, and 3 mol% or more is further preferable. The proportion of the polymerizable functional group is preferably 70 mol% or less, more preferably 60 mol% or less, still more preferably 50 mol% or less, from the viewpoint of obtaining good charge transportability. The "ratio of polymerizable functional groups" here means the ratio of structural units having polymerizable functional groups.

Considering the balance of charge transportability, durability, productivity, etc., the ratio (molar ratio) of the structural unit L and the structural unit T is preferably L: T = 100: 1 to 70, more preferably 100: 3 to 50. It is preferable, and 100: 5 to 30 is more preferable. When the charge transporting polymer contains the structural unit B, the ratio (molar ratio) of the structural unit L, the structural unit T, and the structural unit B is L: T: B = 100: 10 to 200: 10 to 100. Preferably, 100: 20 to 180: 20 to 90 is more preferable, and 100: 40 to 160: 30 to 80 is even more preferable. Here, the structural unit L means the total of the structural unit L1 having a triazine ring and the other structural unit L2 introduced as needed. Further, the structural unit B means the total of the structural unit B1 having a triazine ring and the other structural unit B2 introduced as needed. Here, the ratio of the structural units L1 and L2 and the ratio of the structural units B1 and B2 are as described above.

The ratio of the structural units can be determined by using the amount of the monomer charged corresponding to each structural unit used for synthesizing the charge-transporting polymer. Further, the ratio of the structural units can be calculated as an average value by using the integrated value of the spectrum derived from each structural unit in the ¹ H NMR spectrum of the charge transport polymer. Since it is simple, when the amount to be charged is clear, the value obtained by using the amount to be charged is preferably adopted.

(Production method)
The charge-transporting polymer can be produced by various synthetic methods and is not particularly limited. For example, known coupling reactions such as Suzuki coupling, Negishi coupling, Sonoto coupling, Still coupling, Buchwald-Hartwig coupling and the like can be used. Suzuki coupling causes a cross-coupling reaction using a Pd catalyst between an aromatic boronic acid derivative and an aromatic halide. According to Suzuki Coupling, a charge-transporting polymer can be easily produced by binding desired aromatic rings to each other.

In the coupling reaction, for example, a Pd (0) compound, a Pd (II) compound, a Ni compound and the like are used as the catalyst. Further, a catalyst species generated by mixing tris (dibenzylideneacetone) dipalladium (0), palladium (II) acetate or the like as a precursor and mixing with a phosphine ligand can also be used. For the method of synthesizing the charge transport polymer, for example, the description of International Publication No. WO2010 / 1405553 can be referred to.

When a charge-transporting polymer is prepared using the Suzuki coupling reaction, an example of a combination of monomer compounds that can be suitably used as a raw material is shown below. In the example of the monomer (L), R is the same as R described above in the structural unit L.

[Dopant]
When the charge transporting material is used to construct the organic electronic device, the charge transporting material may further contain an additive known as an organic electronic material. In one embodiment, the charge transport material may further contain a dopant. The dopant is not particularly limited as long as it can exhibit a doping effect and improve the charge transportability by being added to the charge transportable material. Doping includes p-type doping and n-type doping. In p-type doping, a substance that acts as an electron acceptor as a dopant is used, and in n-type doping, a substance that acts as an electron donor as a dopant is used. It is preferable to perform p-type doping for improving hole transportability and n-type doping for improving electron transportability. The dopant used in the charge transport material may be a dopant that exhibits either the p-type doping or the n-type doping effect. Further, one kind of dopant may be added alone, or a plurality of kinds of dopants may be mixed and added.

The dopant used for p-type doping is an electron-accepting compound, and examples thereof include Lewis acid, protonic acid, transition metal compound, ionic compound, halogen compound, and π-conjugated compound. Specifically, as Lewis acid, FeCl ₃ , PF ₅ , AsF ₅ , SbF ₅ , BF ₅ , BCl ₃ , BBr _3, etc .; as sulfonic acid, HF, HCl, HBr, HNO ₅ , H ₂ SO ₄ , inorganic acids such as HClO _4, benzenesulfonic acid, p- toluenesulfonic acid, dodecylbenzenesulfonic acid, polyvinyl sulfonic acid, methanesulfonic acid, trifluoromethanesulfonic acid, trifluoroacetic acid, 1-butane sulfonic acid, vinyl phenyl sulfonate , Organic acids such as camphorsulfonic acid; as transition metal compounds, FeOCl, TiCl ₄ , ZrCl ₄ , HfCl ₄ , NbF ₅ , AlCl ₃ , NbCl ₅ , TaCl ₅ , MoF ₅ ; as ionic compounds, tetrakis (pentafluoro) phenyl) borate, tris (trifluoromethanesulfonyl) Mechidoion, bis (trifluoromethanesulfonyl) imide ion, hexafluoroantimonate ion, AsF ₆ ^- (hexafluoro arsenic acid ions), BF ₄ ^- (tetrafluoroborate), PF ₆ ^- salt having a perfluoroalkyl anions of (hexafluorophosphate) and the like, salts such as having a conjugate base of the protonic acid as anion; halogen _{compounds, Cl 2, Br 2, I} 2, ICl, ICl 3, IBr, IF, etc .; Examples of the π-conjugated compound include TCNE (tetracyanoethylene) and TCNQ (tetracyanoquinodimethane). It is also possible to use the electron-accepting compounds described in JP-A-2000-36390, JP-A-2005-75948, JP-A-2003-213002, and the like. Preferred are Lewis acid, ionic compounds, π-conjugated compounds and the like.

The dopant used for n-type doping is an electron-donating compound, for example, an alkali metal such as Li, Cs; an alkaline earth metal such as Mg, Ca; an alkali metal such as LiF, Cs ₂ CO _3, and / or Alkaline earth metal salts; metal complexes; electron-donating organic compounds and the like.

When the charge-transporting polymer has a polymerizable functional group, it is preferable to use a compound that can act as a polymerization initiator for the polymerizable functional group as the dopant in order to facilitate the change in the solubility of the organic layer.

[Other optional ingredients]
The charge transporting material may further contain a charge transporting low molecular weight compound, another polymer and the like.

[Content]
From the viewpoint of obtaining good charge transportability, the content of the charge transport polymer is preferably 50% by mass or more, more preferably 70% by mass or more, and 80% by mass or more, based on the total mass of the charge transport material. More preferred. It is also possible to make it 100% by mass.

When the dopant is contained, the content thereof is preferably 0.01% by mass or more, preferably 0.1% by mass, based on the total mass of the charge-transporting material from the viewpoint of improving the charge-transporting property of the charge-transporting material. The above is more preferable, and 0.5% by mass or more is further preferable. Further, from the viewpoint of maintaining good film-forming property, 50% by mass or less is preferable, 30% by mass or less is more preferable, and 20% by mass or less is further preferable with respect to the total mass of the charge transporting material.

<Ink composition>
The ink composition according to the embodiment of the present invention contains the charge transporting material of the above embodiment and a solvent capable of dissolving or dispersing the material. By using the ink composition, the organic layer can be easily formed by a simple method such as a coating method.

[solvent]
As the solvent, water, an organic solvent, or a mixed solvent thereof can be used. Examples of the organic solvent include alcohols such as methanol, ethanol and isopropyl alcohol; alkanes such as pentane, hexane and octane; cyclic alkanes such as cyclohexane; aromatic hydrocarbons such as benzene, toluene, xylene, mesitylene, tetraline and diphenylmethane; ethylene glycol. Alibo ethers such as dimethyl ether, ethylene glycol diethyl ether, propylene glycol-1-monomethyl ether acetate; 1,2-dimethoxybenzene, 1,3-dimethoxybenzene, anisole, phenetol, 2-methoxytoluene, 3-methoxytoluene, Aromatic ethers such as 4-methoxytoluene, 2,3-dimethylanisole and 2,4-dimethylanisole; aliphatic esters such as ethyl acetate, n-butyl acetate, ethyl lactate and n-butyl lactate; phenyl acetate, propionic acid Aromatic esters such as phenyl, methyl benzoate, ethyl benzoate, propyl benzoate, n-butyl benzoate; amide solvents such as N, N-dimethylformamide, N, N-dimethylacetamide; dimethylsulfoxide, tetrahydrofuran, acetone , Chloroform, methylene chloride and the like. Aromatic hydrocarbons, aliphatic esters, aromatic esters, aliphatic ethers, aromatic ethers and the like are preferable.

[Polymerization initiator]
When the charge-transporting polymer has a polymerizable functional group, the ink composition preferably contains a polymerization initiator. As the polymerization initiator, known radical polymerization initiators, cationic polymerization initiators, anionic polymerization initiators and the like can be used. From the viewpoint that the ink composition can be easily prepared, it is preferable to use a substance having both a function as a dopant and a function as a polymerization initiator. Examples of such a substance include the above-mentioned ionic compounds.

[Additive]
The ink composition may further contain an additive as an optional component. Additives include, for example, polymerization inhibitors, stabilizers, thickeners, gelling agents, flame retardants, antioxidants, antioxidants, oxidizing agents, reducing agents, surface modifiers, emulsifiers, defoamers, etc. Dispersants, surfactants and the like can be mentioned.

[Content]
The content of the solvent in the ink composition can be determined in consideration of application to various coating methods. For example, the content of the solvent is preferably such that the ratio of the charge transporting polymer to the solvent is 0.1% by mass or more, more preferably 0.2% by mass or more, and 0.5% by mass or more. Is more preferable. The content of the solvent is preferably such that the ratio of the charge-transporting polymer to the solvent is 20% by mass or less, more preferably 15% by mass or less, and further preferably 10% by mass or less. ..

<Organic layer>
The organic layer according to the embodiment of the present invention is a layer formed by using the charge transporting material or the ink composition of the above embodiment. By using the ink composition, the organic layer can be satisfactorily formed by the coating method. Examples of the coating method include a spin coating method; a casting method; a dipping method; a letterpress printing, a concave plate printing, an offset printing, a flat plate printing, a letterpress reversal offset printing, a screen printing, a plate printing method such as gravure printing; an inkjet method and the like. Known methods such as a plateless printing method can be mentioned. When the organic layer is formed by the coating method, the organic layer (coating layer) obtained after coating may be dried using a hot plate or an oven to remove the solvent.

When the charge-transporting polymer has a polymerizable functional group, the polymerization reaction of the charge-transporting polymer can be allowed to proceed by light irradiation, heat treatment, or the like, and the solubility of the organic layer can be changed. By stacking organic layers having different solubilities, it is possible to easily increase the number of layers of organic electronic devices. For the method of forming the organic layer, for example, the description of International Publication No. WO2010 / 1405553 can be referred to.

The thickness of the organic layer after drying or curing is preferably 0.1 nm or more, more preferably 1 nm or more, still more preferably 3 nm or more, from the viewpoint of improving the efficiency of charge transport. The thickness of the organic layer is preferably 300 nm or less, more preferably 200 nm or less, and further preferably 100 nm or less from the viewpoint of reducing the electrical resistance.

<Organic electronics element>
The organic electronic device according to the embodiment of the present invention has at least the organic layer of the above embodiment. Examples of the organic electronics element include an organic EL element, an organic photoelectric conversion element, an organic transistor and the like. The organic electronics element preferably has a structure in which an organic layer is arranged between at least a pair of electrodes.

[Organic EL element]
The organic EL device according to the embodiment of the present invention has at least the organic layer of the above embodiment. The organic EL element usually includes a light emitting layer, an anode, a cathode, and a substrate, and if necessary, provides other functional layers such as a hole injection layer, an electron injection layer, a hole transport layer, and an electron transport layer. I have. Each layer may be formed by a vapor deposition method or a coating method. The organic EL device preferably has an organic layer as a light emitting layer or another functional layer, more preferably as a functional layer, and further preferably as at least one of a hole injection layer and a hole transport layer.

FIG. 1 is a schematic cross-sectional view showing an embodiment of an organic EL device. The organic EL element of FIG. 1 is an element having a multi-layer structure, and includes a substrate 8, an anode 2, a hole injection layer 3 and a hole transport layer 6 composed of the organic layer of the above embodiment, a light emitting layer 1, and an electron transport layer 7. It has an electron injection layer 5 and a cathode 4 in this order. Hereinafter, each layer will be described.

[Hole injection layer, hole transport layer]
In FIG. 1, the hole injection layer 3 and the hole transport layer 6 are organic layers formed by using the charge transporting material or the ink composition, but the organic EL element is not limited to such a structure. The other organic layer may be a layer formed by using the charge transporting material or the ink composition. At least one of the hole transport layer and the hole injection layer is preferably an organic layer formed by using the charge transporting material or the ink composition, and at least the hole transport layer is further said to be the organic layer. preferable. For example, when the organic EL device has an organic layer formed by using the charge transporting material or the ink composition as a hole transport layer and further has a hole injection layer, the hole injection layer is known. Materials can be used. Further, for example, when the organic EL element has an organic layer formed by using the charge transporting material or the ink composition as a hole injection layer and further has a hole transport layer, the hole transport layer may be a hole transport layer. Known materials can be used.

[Light emitting layer]
As the material used for the light emitting layer, a light emitting material such as a low molecular weight compound, a polymer, or a dendrimer can be used. Polymers are preferred because they are highly soluble in solvents and suitable for coating methods. Examples of the light emitting material include a fluorescent material, a phosphorescent material, a heat-activated delayed fluorescent material (TADF), and the like.

Low molecular weight compounds such as perylene, coumarin, rubrene, quinacdrine, stilben, dye for dye laser, aluminum complex, and derivatives thereof as fluorescent materials; polyfluorene, polyphenylene, polyphenylene vinylene, polyvinylcarbazole, fluorene-benzothiazol copolymer , Fluorene-triphenylamine copolymers, polymers such as derivatives thereof; mixtures thereof and the like.

As the phosphorescent material, a metal complex containing a metal such as Ir or Pt can be used. Examples of the Ir complex include FIr (pic) (iridium (III) bis [(4,6-difluorophenyl) -pyridinate-N, C ² ] picolinate) that emits blue light, and Ir (ppy) ₃ that emits green light. (Factris (2-phenylpyridine) iridium), emits red light (btp) ₂ Ir (acac) (bis [2- (2'-benzo [4,5-α] thienyl) pyridinate-N, C ³ ] Examples thereof include iridium (acetyl-acetonate)) and Ir (piq) ₃ (tris (1-phenylisoquinolin) iridium). Examples of the Pt complex include PtOEP (2, 3, 7, 8, 12, 13, 17, 18-octaethyl-21H, 23H-forfin platinum) that emits red light.

When the light emitting layer contains a phosphorescent material, it is preferable to further contain a host material in addition to the phosphorescent material. As the host material, a low molecular weight compound, a polymer, or a dendrimer can be used. Examples of low molecular weight compounds include CBP (4,4'-bis (9H-carbazole-9-yl) biphenyl), mCP (1,3-bis (9-carbazolyl) benzene), and CDBP (4,4'-. Bis (carbazole-9-yl) -2,2'-dimethylbiphenyl), derivatives thereof and the like, and as the polymer, the charge transporting material of the above embodiment, polyvinylcarbazole, polyphenylene, polyfluorene, derivatives thereof and the like can be used. Can be mentioned.

Examples of the heat-activated delayed fluorescent material include Adv. Mater., 21, 4802-4906 (2009); Appl. Phys. Lett., 98, 083302 (2011); Chem. Comm., 48, 9580 (2012). Appl. Phys. Lett., 101, 093306 (2012); J. Am. Chem. Soc., 134, 14706 (2012); Chem. Comm., 48, 11392 (2012); Nature, 492, 234 (2012) ); Adv. Mater., 25, 3319 (2013); J. Phys. Chem. A, 117, 5607 (2013); Phys. Chem. Chem. Phys., 15, 15850 (2013); Chem. Comm., 49, 10385 (2013); Chem. Lett., 43, 319 (2014) and the like.

[Electron transport layer, electron injection layer]
Examples of the material used for the electron transport layer and the electron injection layer include fused ring tetracarboxylic acid anhydrides such as phenanthroline derivative, bipyridine derivative, nitro-substituted fluorene derivative, diphenylquinone derivative, thiopyrandioxide derivative, naphthalene and perylene, and carbodiimide. , Fluolenilidene methane derivative, anthraquinodimethane and antron derivative, oxadiazole derivative, thiadiazole derivative, benzoimidazole derivative, quinoxalin derivative, aluminum complex and the like. Further, the charge transporting material of the above embodiment can also be used.

[cathode]
As the cathode material, for example, a metal or a metal alloy such as Li, Ca, Mg, Al, In, Cs, Ba, Mg / Ag, LiF, CsF is used.

[anode]
As the anode material, for example, a metal (for example, Au) or another material having conductivity is used. Other materials include, for example, oxides (eg, ITO: indium oxide / tin oxide), conductive polymers (eg, polythiophene-polystyrene sulfonic acid mixture (PEDOT: PSS)).

[substrate]
Glass, plastic, etc. can be used as the substrate. The substrate is preferably transparent and preferably has flexibility. Quartz glass, light-transmitting resin film and the like are preferably used.

Examples of the resin film include films made of polyethylene terephthalate, polyethylene naphthalate, polyether sulfone, polyetherimide, polyetherether ketone, polyphenylene sulfide, polyarylate, polyimide, polycarbonate, cellulose triacetate, cellulose acetate propionate and the like. Can be mentioned.

When a resin film is used, the resin film may be coated with an inorganic substance such as silicon oxide or silicon nitride in order to suppress the permeation of water vapor, oxygen and the like.

[Emission color]
The emission color of the organic EL element is not particularly limited. The white organic EL element is preferable because it can be used for various lighting fixtures such as household lighting, vehicle interior lighting, clocks, and liquid crystal backlights.

As a method for forming a white organic EL element, a method can be used in which a plurality of luminescent materials are used to simultaneously emit a plurality of luminescent colors to mix the colors. The combination of a plurality of emission colors is not particularly limited, but a combination containing three emission maximum wavelengths of blue, green and red, and two emission maximum wavelengths such as blue and yellow, yellowish green and orange are used. Examples include the combination contained. The emission color can be controlled by adjusting the type and amount of the emission material.

<Display element, lighting device, display device>
The display element according to the embodiment of the present invention includes the organic EL element according to the above embodiment. For example, a color display element can be obtained by using an organic EL element as an element corresponding to each pixel of red, green, and blue (RGB). There are two methods for forming an image: a simple matrix type in which individual organic EL elements arranged on a panel are directly driven by electrodes arranged in a matrix, and an active matrix type in which a thin film transistor is arranged and driven in each element.

Further, the lighting device according to the embodiment of the present invention includes the organic EL element according to the embodiment of the present invention. Further, the display device according to the embodiment of the present invention includes a lighting device and a liquid crystal element as a display means. For example, the display device can be a display device using a lighting device according to an embodiment of the present invention as a backlight and a known liquid crystal element as a display means, that is, a liquid crystal display device.

(Example)
Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited to the following Examples.

<1> Preparation of charge-transporting polymer (preparation of Pd catalyst)
Tris (dibenzylideneacetone) dipalladium (73.2 mg, 80 μmol) was weighed in a sample tube at room temperature in a glove box under a nitrogen atmosphere, anisole (15 mL) was added, and the mixture was stirred for 30 minutes. Similarly, tris (t-butyl) phosphine (129.6 mg, 640 μmol) was weighed into a sample tube, anisole (5 mL) was added, and the mixture was stirred for 5 minutes. These solutions were mixed and stirred at room temperature for 30 minutes to give a catalyst solution. In the preparation of the catalyst, all the solvents were used after being degassed by nitrogen bubbles for 30 minutes or more.

(Preparation Example 1) Charge-transporting polymer 1
The following monomer 1 (4.0 mmol), the following monomer 2 (5.0 mmol), the following monomer 3 (2.0 mmol), and anisole (20 mL) are added to a three-necked round bottom flask, and a separately prepared Pd catalyst solution is added. (7.5 mL) was added and stirred. After stirring for 30 minutes, a 10% tetraethylammonium hydroxide aqueous solution (20 mL) was added to the flask. The mixture was heated to reflux for 2 hours. All the operations up to this point were performed under a nitrogen stream. In addition, all solvents were used after being degassed by nitrogen bubbles for 30 minutes or more.

After completion of the reaction, the organic layer was washed with water. The organic layer was then poured into methanol-water (9: 1). The resulting precipitate was suction filtered and washed with methanol-water (9: 1). The washed precipitate was dissolved in toluene and reprecipitated from methanol. The obtained precipitate is suction-filtered, then dissolved in toluene, and Triphenylphosphine, polymer-bound on styrene-divinylbenzene copolymer (Strem Chemicals, 200 mg per 100 mg of polymer, hereinafter referred to as "metal adsorbent") is added. Stirred overnight.
After the stirring was completed, the metal adsorbent and the insoluble matter were removed by filtration, and the filtrate was concentrated on a rotary evaporator. The concentrate was dissolved in toluene and then reprecipitated from methanol-acetone (8: 3). The resulting precipitate was suction filtered and washed with methanol-acetone (8: 3). The obtained precipitate was vacuum dried to obtain a charge-transporting polymer 1.
The obtained charge-transporting polymer 1 had a number average molecular weight of 7,800 and a weight average molecular weight of 31,000. The molecular weight was measured by GPC (polystyrene conversion) using THF as an eluent. The charge-transporting polymer 1 includes a triazine or higher valent structural unit B2 (derived from monomer 3) containing no triazine ring, a divalent structural unit L2 (derived from monomer 2) containing no triazine ring, and a polymerizable functional unit. It contained a monovalent structural unit T (derived from monomer 1) having a group, and the proportions of each structural unit were 18.2%, 45.5%, and 36.4%, respectively.

The measurement conditions for the number average molecular weight and the weight average molecular weight are as follows.
Liquid transfer pump: L-6050 Hitachi High-Technologies Corporation
UV-Vis detector: L-3000 Hitachi High-Technologies Corporation Column: Gelpack (registered trademark) GL-A160S / GL-A150S Hitachi Chemical Co., Ltd.
Eluent: THF (manufactured by Wako Pure Chemical Industries, Ltd., for HPLC, no stabilizer)
Flow velocity: 1 mL / min
Column temperature: Room temperature Molecular weight standard substance: Standard polystyrene

(Preparation Example 2) Charge Transport Polymer 2
Monomer 2 (5.0 mmol) and monomer 3 (2.0 mmol) described in Preparation Example 1, the following monomer 4 (4.0 mmol), and anisole (20 mL) are added to a three-necked round bottom flask, and further prepared separately. A solution of the Pd catalyst (7.5 mL) was added, and the mixture was stirred. After that, the charge transporting polymer 2 was prepared in the same manner as described in Preparation Example 1.
The obtained charge-transporting polymer 2 had a number average molecular weight of 22,900 and a weight average molecular weight of 169,000. The charge-transporting polymer 2 comprises a triazine ring-free trivalent or higher valent structural unit B2 (derived from monomer 3), a triazine ring-free divalent structural unit L2 (derived from monomer 2), and a monovalent structure. The proportion of each structural unit, including structural unit T (derived from monomer 4), was 18.2%, 45.5%, and 36.4%, respectively.

(Preparation Example 3) Charge Transport Polymer 3
In a three-necked round bottom flask, the monomer 2 (5.0 mmol) described in Preparation Example 1, the monomer 4 (4.0 mmol) described in Preparation Example 2, the following monomer 5 (2.0 mmol), and anisole (20 mL) were added. Was added, a solution of the Pd catalyst prepared separately (7.5 mL) was further added, and the mixture was stirred. After that, the charge transport polymer 3 was prepared in the same manner as described in Preparation Example 1.
The obtained charge-transporting polymer 3 had a number average molecular weight of 6,300 and a weight average molecular weight of 50,600. The charge-transporting polymer 3 has a triazine or higher valent structural unit B1 (derived from monomer 5) having a triazine ring, a divalent structural unit L2 (derived from monomer 2) not containing a triazine ring, and a monovalent structure. The proportion of each structural unit, including the unit T (derived from monomer 4), was 18.2%, 45.5%, and 36.4%, respectively.

(Preparation Example 4) Charge Transport Polymer 4
The charge-transporting polymer 4 was prepared in the same manner as in Preparation Example 3 except that the monomer 6 was used instead of the monomer 2.
The obtained charge-transporting polymer 4 had a number average molecular weight of 4,300 and a weight average molecular weight of 30,900. The charge-transporting polymer 4 has a triazine or higher valent structural unit B1 (derived from monomer 5) having a triazine ring, a divalent structural unit L2 (derived from monomer 6) not containing a triazine ring, and a monovalent structure. The proportion of each structural unit, including the unit T (derived from monomer 4), was 18.2%, 45.5%, and 36.4%, respectively.

(Preparation Example 5) Charge Transport Polymer 5
The charge transport polymer 5 was prepared in the same manner as in Preparation Example 3 except that the monomer 4 (4.0 mmol) was changed to the monomer 4 (2.0 mmol) and the monomer 1 (2.0 mmol).
The obtained charge-transporting polymer 5 had a number average molecular weight of 6,500 and a weight average molecular weight of 55,900. The charge-transporting polymer 5 has a triazine ring-bearing trivalent or higher structural unit B1 (derived from monomer 5) and a triazine ring-free divalent structural unit L2 (derived from monomer 2), a monovalent structural unit. It contains T (derived from monomer 4) and monovalent structural unit T (derived from monomer 1) having a polymerizable functional group, and the proportions of each structural unit are 18.2% and 45.5%, respectively. , 18.2%, and 18.2%.

(Preparation Example 6) Charge Transport Polymer 6
In a three-necked round bottom flask, the monomer 2 (5.0 mmol) described in Preparation Example 1, the monomer 4 (2.0 mmol) described in Preparation Example 2, the following monomer 7 (4.0 mmol), and anisole (20 mL) were added. Was added, a solution of the Pd catalyst prepared separately (7.5 mL) was further added, and the mixture was stirred. After that, the charge-transporting polymer 6 was prepared in the same manner as described in Preparation Example 1.
The obtained charge-transporting polymer 6 had a number average molecular weight of 5,500 and a weight average molecular weight of 8,700. The charge-transporting polymer 6 comprises a divalent structural unit L1 having a triazine ring (derived from monomer 7), a divalent structural unit L2 containing no triazine ring (derived from monomer 2), and a monovalent structural unit. The proportions of each structural unit containing T (derived from monomer 4) were 36.4%, 45.5%, and 18.2%, respectively.

(Preparation Example 7) Charge-transporting polymer 7
Preparation Example 3 except that monomer 5 (2.0 mmol) was changed to monomer 5 (0.75 mmol) and monomer 7 (2.25 mmol), monomer 2 was used at 4.5 mmol, and monomer 4 was used at 2.25 mmol. The charge transport polymer 7 was prepared in the same manner.
The obtained charge-transporting polymer 7 had a number average molecular weight of 6,300 and a weight average molecular weight of 47,200. The charge-transporting polymer 7 does not contain a triazine or higher valent structural unit B1 (derived from monomer 5) having a triazine ring, a divalent structural unit L1 having a triazine ring (derived from monomer 7), and a triazine ring 2. It contains the valence structural unit L2 (derived from monomer 2) and the monovalent structural unit T (derived from monomer 4), and the proportions of each structural unit are 7.7%, 23.1%, and 46, respectively. It was .2% and 23.1%.

(Preparation Example 8) Charge-transporting polymer 8
The charge transport polymer 8 was prepared in the same manner as in Preparation Example 3 except that the monomer 8 was used instead of the monomer 5.
The obtained charge-transporting polymer 8 had a number average molecular weight of 5,300 and a weight average molecular weight of 33,700. The charge-transporting polymer 8 has a triazine or higher valent structural unit B1 (derived from monomer 8) having a triazine ring, a divalent structural unit L2 (derived from monomer 2) not containing a triazine ring, and a monovalent structure. The proportion of each structural unit, including the unit T (derived from monomer 4), was 18.2%, 45.5%, and 36.4%, respectively.

<2-1> Fabrication of Organic EL Element (Example 1)
The charge-transporting polymer 1 (10.0 mg) obtained by synthesizing the above-mentioned charge-transporting polymer, the following ionic compound (0.5 mg), on a glass substrate in which ITO is patterned to a width of 1.6 mm under a nitrogen atmosphere. Ink composition 1 composed of and toluene (2.3 mL) was spin-coated at 3000 min ^-1 and then heated on a hot plate at 220 ° C. for 10 minutes to cure to form a hole injection layer (30 nm).

Next, on the hole injection layer obtained by the above operation, an ink composition 3 composed of the charge transport polymer 3 (20 mg), the above ionic compound (1.0 mg), and toluene (2.3 mL) was added. After spin coating at 3000 min- ¹ , the hole transport layer (40 nm) was formed by heating on a hot plate at 180 ° C. for 10 minutes to dry. The hole transport layer could be formed without dissolving the hole injection layer.

The substrate obtained above is transferred into a vacuum vapor deposition machine, and CBP: Ir (ppy) ₃ (94: 6, 30 nm), BAlq (10 nm), Alq ₃ (30 nm), LiF (0) are placed on the hole transport layer. A film was formed in the order of 0.8 nm) and Al (100 nm) by a vapor deposition method, and a sealing treatment was performed to prepare an organic EL device.

(Example 2)
In Example 1, an ink composition 4 was prepared in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer in the organic EL device was changed to the charge-transporting polymer 4. An organic EL device was produced in the same manner as in Example 1 except that the hole transport layer was formed using this ink composition 4.

(Example 3)
In Example 1, an ink composition 5 was prepared in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer in the organic EL device was changed to the charge-transporting polymer 5. An organic EL device was produced in the same manner as in Example 1 except that the hole transport layer was formed using this ink composition 5.

(Example 4)
In Example 1, an ink composition 6 was prepared in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer in the organic EL device was changed to the charge-transporting polymer 6. An organic EL device was produced in the same manner as in Example 1 except that the hole transport layer was formed using this ink composition 6.

(Example 5)
In Example 1, an ink composition 7 was prepared in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer in the organic EL device was changed to the charge-transporting polymer 7. An organic EL device was produced in the same manner as in Example 1 except that the hole transport layer was formed using this ink composition 7.

(Example 6)
In Example 1, an ink composition 8 was prepared in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer in the organic EL device was changed to the charge-transporting polymer 8. An organic EL device was produced in the same manner as in Example 1 except that the hole transport layer was formed using this ink composition 8.

(Comparative Example 1)
In Example 1, an ink composition 2 was prepared in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer in the organic EL device was changed to the charge-transporting polymer 2. An organic EL device was produced in the same manner as in Example 1 except that the hole transport layer was formed using this ink composition 2.

<2-2> Evaluation of Organic EL Element When a voltage was applied to the organic EL element obtained in Examples 1 to 6 and Comparative Example 1, green light emission was confirmed in both cases. For each element, emission luminance 1000 cd / ^{m 2} at the drive voltage and luminous efficiency were measured emission lifetime (luminance half-life) in the initial luminance 3000 cd / ^{m 2.} The measurement results are shown in Table 2.

As shown in Table 2, the organic EL devices of Examples 1 to 6 had a lower drive voltage, excellent luminous efficiency, and a longer luminous life than Comparative Example 1. That is, from the viewpoint of the constituent material of the hole transport layer, by using a charge transport polymer having a structural unit containing a triazine ring in the molecule as the charge transport material, the luminous efficiency and the light emission life are improved. It can be seen that the effect can be obtained.

<3-1> Fabrication of white organic EL element (lighting device) (Example 7)
As in Example 1, a charge-transporting polymer 1 (10.0 mg), an ionic compound (0.5 mg), and toluene (2) were placed on a glass substrate in which ITO was patterned to a width of 1.6 mm under a nitrogen atmosphere. The ink composition 1 consisting of .3 mL) was spin-coated at 3000 min ^-1 and then heated on a hot plate at 220 ° C. for 10 minutes to cure to form a hole injection layer (30 nm).

Next, in the same manner as in Example 1, the hole injection layer obtained by the above operation is composed of the charge-transporting polymer 3 (20 mg), the ionic compound (1.0 mg), and toluene (2.3 mL). The ink composition 3 was spin-coated at 3000 min ^-1 and then heated on a hot plate at 180 ° C. for 10 minutes to cure to form a hole transport layer (40 nm). The hole transport layer could be formed without dissolving the hole injection layer.

Next, in nitrogen, CDBP (15 mg), FIR (pic) (0.9 mg), Ir (ppy) ₃ (0.9 mg), (btp) ₂ Ir (acac) (1.2 mg), and dichlorobenzene ( The mixture (0.5 mL) was spin coated at 3000 min ^-1 and then dried at 80 ° C. for 5 minutes to form a light emitting layer (40 nm). Further, BAlq (10 nm), Alq ₃ (30 nm), LiF (0.5 nm), and Al (100 nm) were vapor-deposited in this order and sealed to prepare a white organic EL device. The white organic EL element could be used as a lighting device. The light emitting layer could be formed without dissolving the hole transport layer.

(Example 8)
In Example 7, the ink composition 4 in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer was changed to the charge-transporting polymer 4 was prepared. A white organic EL device was produced in the same manner as in Example 7 except that the hole transport layer was formed using the ink composition 4.

(Example 9)
In Example 7, an ink composition 5 was prepared in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer was changed to the charge-transporting polymer 5. A white organic EL device was produced in the same manner as in Example 7 except that the hole transport layer was formed using this ink composition 5.

(Example 10)
In Example 7, an ink composition 6 was prepared in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer was changed to the charge-transporting polymer 6. A white organic EL device was produced in the same manner as in Example 7 except that the hole transport layer was formed using this ink composition 6.

(Example 11)
In Example 7, an ink composition 7 was prepared in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer was changed to the charge-transporting polymer 7. A white organic EL device was produced in the same manner as in Example 7 except that the hole transport layer was formed using this ink composition 7.

(Example 12)
In Example 7, an ink composition 8 was prepared in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer was changed to the charge-transporting polymer 8. A white organic EL device was produced in the same manner as in Example 7 except that the hole transport layer was formed using this ink composition 8.

(Comparative Example 2)
In Example 7, an ink composition 2 was prepared in which the charge-transporting polymer 3 in the ink composition 3 used for forming the hole transport layer was changed to the charge-transporting polymer 2. A white organic EL device was produced in the same manner as in Example 7 except that the hole transport layer was formed using this ink composition 2.

<3-2> Evaluation of white organic EL element (lighting device) A voltage is applied to the white organic EL element obtained in Examples 7 to 12 and Comparative Example 2, and the driving voltage and light emission at an initial brightness of 1000 cd / m ^2. Efficiency and luminous life were measured. Table 3 shows the drive voltage, luminous efficiency, and luminous life of Examples 7 to 12 when the driving voltage, luminous efficiency, and luminous life of Comparative Example 2 are set to 1, respectively.

As shown in Table 3, the white organic EL devices of Examples 7 to 12 were superior in luminous efficiency and light emitting life as compared with the white organic EL devices of Comparative Example 2. That is, from the viewpoint of the constituent material of the hole transport layer, the luminous efficiency and the luminous life are improved by using the charge transport polymer having a structural unit containing a triazine ring in the molecule as the charge transport material. It can be seen that such an effect can be obtained.

As described above, the effects of the embodiments of the present invention are shown by the examples. However, according to the present invention, the organic electronics are not limited to the charge-transporting polymer used in the examples, and even when other charge-transporting polymers are used as long as they do not deviate from the scope of the present invention. It is possible to obtain an element. The obtained organic electronic device has excellent characteristics as in each of the above embodiments.

1 Light emitting layer 2 Anode 3 Hole injection layer 4 Cathode 5 Electron injection layer 6 Hole transport layer 7 Electron transport layer 8 Substrate

Claims (12)

A divalent structure having charge transportability other than the trivalent structural unit B1 having a triazine ring represented by the following formula, the divalent structural unit L1 having a triazine ring, and the divalent structural unit L1 having the triazine ring. A charge-transporting material containing a charge-transporting polymer and used as a hole-transporting material, which comprises at least one of the structural units L2.

[In the formula, Ar is a substituted or unsubstituted arylene group having 6 to 30 carbon atoms. ] The charge transporting material according to claim 1, wherein the charge transporting polymer comprises a trivalent structural unit B1 having a triazine ring in which Ar is an independently substituted or unsubstituted phenylene group or naphthylene group. Claim 1 or 2 wherein the charge-transporting divalent structural unit L2 includes a structure selected from the group consisting of an aromatic amine structure, a carbazole structure, a thiophene structure, a bithiophene structure, a benzene structure, and a fluorene structure. The charge transporting material according to. The charge-transporting material according to claim 1 or 2, wherein the divalent structural unit L2 having charge-transporting property includes a structure selected from the group consisting of an aromatic amine structure and a carbazole structure. An ink composition containing the charge-transporting material according to any one of claims 1 to 4 and a solvent. An organic electronic device having an organic layer containing the charge transporting material according to any one of claims 1 to 4 . An organic electroluminescent device having an organic layer containing the charge-transporting material according to any one of claims 1 to 4 . The organic electroluminescence device according to claim 7 , further comprising a flexible substrate. The organic electroluminescence device according to claim 8 , wherein the flexible substrate contains a resin film. A display device including the organic electroluminescence device according to any one of claims 7 to 9 . A lighting device comprising the organic electroluminescence device according to any one of claims 7 to 9 . A display device including the lighting device according to claim 11 and a liquid crystal element as a display means.

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