KR20230136039A - Polycyclic Aromatic Compound - Google Patents

Abstract

Provided is a novel compound useful as a material for an organic device like an organic electroluminescent element. Provided is a polycyclic aromatic compound having a structure containing a structural unit represented by formula (1) or formula (2), in which: B to I rings are substituted/unsubstituted aryl rings or substituted/unsubstituted heteroaryl rings; C ring and D ring are bonded or not bonded at the position of a broken line; Z is -CH= or -N=; x is independently >N-R^NX (R^NX is aryl or the like); Y is >B-; at least one selected from the group consisting of an aryl ring or a heteroaryl ring in the structure may be condensed with at least one cycloalkane; and at least one hydrogen in the above mentioned structure may be replaced with cyano, halogen or deuterium.

Description

Polycyclic Aromatic Compound}

The present invention relates to polycyclic aromatic compounds. The present invention also relates to organic devices using the polycyclic aromatic compound, such as organic electroluminescent elements, organic field effect transistors, and organic thin-film solar cells, and display devices and lighting devices.

Conventionally, display devices using light-emitting elements that emit electroluminescence have been studied in various ways because they enable lower power consumption and reduction in thickness. Additionally, organic electroluminescent elements made of organic materials have been actively studied because they are easy to reduce in weight and size. In particular, regarding the development of organic materials with luminescent properties such as blue, one of the three primary colors of light, and the development of organic materials with charge transport capabilities such as holes and electrons (with the potential to become semiconductors or superconductors), polymer compounds , regardless of low molecular weight compounds, have been actively studied so far.

An organic electroluminescent element has a structure consisting of a pair of electrodes consisting of an anode and a cathode, and one or multiple layers disposed between the pair of electrodes and containing an organic compound. Layers containing organic compounds include a light-emitting layer and a charge transport/injection layer that transports or injects charges such as holes and electrons, and various organic materials suitable for these layers are being developed.

Among them, Patent Documents 1 to 3 disclose that polycyclic aromatic compounds containing boron are useful as materials for organic electroluminescent devices and the like. It has been reported that organic electroluminescent devices containing this polycyclic aromatic compound have good external quantum efficiency.

International Publication No. 2015/102118 International Publication No. 2020/162600 International Publication No. 2022/034916

As described above, various materials have been developed as materials for use in organic EL devices. However, in order to increase the selection of materials for organic EL devices, the development of materials made of compounds different from those of the past is expected.

The object of the present invention is to provide novel compounds useful as materials for organic devices such as organic EL elements.

In order to solve the above problems, the present inventors have conducted intensive studies to produce a novel polyaromatic compound that has a boron-containing structure similar to the compounds described in Patent Documents 1 to 3, has excellent luminescence properties, and has a characteristic luminescence wavelength. was successful. Furthermore, it was discovered that an excellent organic EL device could be obtained by disposing a layer containing this polycyclic aromatic compound between a pair of electrodes to form an organic EL device, and the present invention was completed. That is, the present invention provides polycyclic aromatic compounds as described below, and further materials for organic devices containing the polycyclic aromatic compounds as described below.

<1> a polycyclic aromatic compound having a structure containing a structural unit represented by formula (1) or formula (2);

In equation (1),

Ring B, ring C, ring D, ring E, ring F, ring G, ring H, and ring I are each independently a substituted or unsubstituted aryl ring or a substituted or unsubstituted heteroaryl ring,

The broken line connecting the C ring and the D ring indicates that the C ring and the D ring are not bonded at the position of the dashed line, or are bonded through a single bond or linking group at the position of the broken line,

Z is -C(-R ^Z )= or -N=, R ^Z is hydrogen or a substituent,

X is ^each independently a single bond, > _NR ^NX , > ^O , >C ( _-R ^C It is substituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CX and R ^IX are each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted. It is substituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and two R ^CX may be bonded to each other to form a ring, and two R ^IX may be bonded to each other to form a ring. R ^NX , R ^CX and R ^IX may each be bonded to one or two rings to which X containing itself is bonded,

Y is each independently, >B-, >P-, >P(=O)-, >P(=S)-, >Al-, >Ga-, >As-, >C(-R ^Y )- , >Si(-R ^Y )-, or >Ge(-R ^Y )-, where R ^Y is each independently optionally substituted aryl, optionally substituted heteroaryl, optionally substituted alkyl, or substituted It is a cycloalkyl that may be

In the above structure, at least one selected from the group consisting of an aryl ring and a heteroaryl ring may be condensed with at least one cycloalkane, and the cycloalkane may be substituted with at least one substituent, and the cycloalkane may be At least one -CH ₂ - in may be substituted with -O-,

At least one hydrogen in the above structure may be substituted with cyano, halogen, or deuterium.

<2> When the B ring, C ring, D ring, E ring, F ring, G ring, H ring, and I ring are each a substituted aryl ring or substituted heteroaryl ring, the substituent is substituent group Z and formula (A30) It is at least one substituent selected from the group consisting of substituents represented by,

Substituent group Z is,

Aryl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl, and cycloalkyl;

heteroaryl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl;

diarylamino which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl (two aryls may be bonded to each other through a linking group);

diheteroarylamino which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl (two heteroaryls may be bonded to each other through a linking group);

Arylheteroarylamino which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl (aryl and heteroaryl may be bonded to each other through a linking group);

diarylboryl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl (two aryls may be bonded through a single bond or linking group);

alkyl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, and cycloalkyl;

Cycloalkyl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl;

alkoxy optionally substituted with at least one group selected from the group consisting of aryl, heteroaryl, and cycloalkyl;

aryloxy which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl, and cycloalkyl; and

Consists of substituted silyl,

In equation (A30),

Ak is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted cycloalkyl, or substituted or unsubstituted cycloalkenyl, and the alkyl, alkenyl, cycloalkyl and cycloalkenyl At least one -CH ₂ - may be substituted with -O- or -S-,

R ^Ak is substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^Ak may be bonded to Ak through a linking group or single bond. , * is the binding position,

The polycyclic aromatic compound described in <1>.

<3> The polycyclic aromatic compound according to <2>, expressed by formula (1).

<4> A polycyclic aromatic compound according to <3>, represented by the following formula (1-b);

In equation (1-b),

Z is each independently -C(-R ^Z )= or -N=,

R ^Z is each independently hydrogen or a substituent,

When R ^Z is a substituent, the substituent is any one selected from the substituent group Z or a substituent represented by the formula (A30),

Two adjacent ^R

Z=Z may each independently be >NR, >O, >C(-R) ₂ , >Si(-R) ₂ , >S, or >Se, wherein the >NR and the >C(-R) ₂ and R of >Si(-R) ₂ is each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, >C(-R) ₂ and the two R of >Si(-R) ₂ may be bonded to each other to form a ring,

X is each independently >NR ^NX , >O, >C(-R ^CX ) ₂ , >S, or >Se, and R ^NX is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, is substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^C It is a cycloalkyl, and two R ^CX may be bonded to each other to form a ring, and R ^NX and R ^CX are each bonded to one or two or more of the You can do it,

L is a single bond, >NR ^NL , >O, >C(-R ^CL ) ₂ , >S, or >Se, and R ^NL is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CL is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl. It is an alkyl, and two R ^CL may be bonded to each other to form a ring, and R ^NL and R ^CL are each bonded to one or two or more of Z bonded to the carbon atom to which L bonded, including itself, You can have it,

In the above structure, at least one aryl ring or heteroaryl ring may be condensed with at least one cycloalkane, the cycloalkane may be substituted with at least one substituent, and at least one substituent in the cycloalkane may be substituted. -CH ₂ - may be substituted with -O-,

At least one hydrogen in the above structure may be substituted with cyano, halogen, or deuterium.

<5> All Zs are -C(-R ^Z )=,

The polycyclic aromatic compound according to <4>, wherein X is each independently >O, >NR ^NX , or >S.

<6> R ^Z is each independently hydrogen, alkyl, phenyl optionally substituted by alkyl, diphenylamino optionally substituted by alkyl, or carbazolyl optionally substituted by alkyl, <4> or <5 > Polycyclic aromatic compounds described in.

<7> A polycyclic aromatic compound according to <3>, expressed by the following formula;

where Me is methyl.

<8> The polycyclic aromatic compound according to <2>, expressed by formula (2).

<9> A polycyclic aromatic compound according to <8>, represented by the following formula (2-b);

In equation (2-b),

Z is each independently -C(-R ^Z )= or -N=,

R ^Z is each independently hydrogen or a substituent,

When R ^Z is a substituent, the substituent is any one selected from the substituent group Z or a substituent represented by the formula (A30),

Two adjacent ^R

Z=Z may each independently be >NR, >O, >C(-R) ₂ , >Si(-R) ₂ , >S, or >Se, wherein the >NR and the >C(-R) ₂ and R of >Si(-R) ₂ is each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, >C(-R) ₂ and the two R of >Si(-R) ₂ may be bonded to each other to form a ring,

X is each independently >NR ^NX , >O, >C(-R ^CX ) ₂ , >S, or >Se, and R ^NX is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, is substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^C It is a cycloalkyl, and two R ^CX may be bonded to each other to form a ring, and R ^NX and R ^CX are each bonded to one or two or more of the You can do it,

L is a single bond, >NR ^NL , >O, >C(-R ^CL ) ₂ , >S, or >Se, and R ^NL is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CL is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl. It is an alkyl, and two R ^CL may be bonded to each other to form a ring, and R ^NL and R ^CL are each bonded to one or two or more of Z bonded to the carbon atom to which L bonded, including itself, You can have it,

In the above structure, at least one aryl ring or heteroaryl ring may be condensed with at least one cycloalkane, the cycloalkane may be substituted with at least one substituent, and at least one substituent in the cycloalkane may be substituted. -CH ₂ - may be substituted with -O-,

At least one hydrogen in the above structure may be substituted with cyano, halogen, or deuterium.

<10> The polycyclic aromatic compound according to <9>, wherein all Zs are -C(-R ^Z )= and Xs are each independently >O, >NR ^NX , or >S.

<11> R ^Z is each independently hydrogen, alkyl, phenyl optionally substituted by alkyl, diphenylamino optionally substituted by alkyl, or carbazolyl optionally substituted by alkyl, <9> or <10 > Polycyclic aromatic compounds described in.

<12> A polycyclic aromatic compound according to <8>, expressed by the following formula;

where Me is methyl.

<13> A polymer compound with a number average molecular weight of 2000 to 1.0×10 ⁸ obtained by polymerizing a reactive compound in which the polycyclic aromatic compound according to any one of <1> to <12> is substituted with a reactive substituent as a monomer.

<14> A material for an organic device containing the polycyclic aromatic compound according to any one of <1> to <12>.

<15> The organic device material according to <14>, wherein the organic device material is a material for an organic electroluminescent element, a material for an organic field effect transistor, a material for an organic thin film solar cell, or a material for a wavelength conversion filter.

<16> Organic electroluminescence, which has a pair of electrodes consisting of an anode and a cathode and an organic layer disposed between the pair of electrodes, wherein the organic layer contains the polycyclic aromatic compound according to any one of <1> to <12>. device.

<17> The organic electroluminescent device according to <16>, wherein the organic layer is a light-emitting layer.

<18> A display or lighting device including the organic electroluminescent element according to <16> or <17>.

<19> A method for producing a polycyclic aromatic compound according to any one of <1> to <12>,

By adding a boronating agent and a Bronsted base to the compound represented by the formula (Int) and reacting it, a mixture of the polycyclic aromatic compound represented by the formula (1) and the polycyclic aromatic compound represented by the formula (2) is obtained. Manufacturing method including;

In the expression (Int),

Ring B, ring C, ring D, ring E, ring F, ring G, ring H, and ring I are each independently a substituted or unsubstituted aryl ring or a substituted or unsubstituted heteroaryl ring,

The broken line connecting the C ring and the D ring indicates that the C ring and the D ring are not bonded at the position of the dashed line, or are bonded through a single bond or linking group at the position of the broken line,

Z is -C(-R ^Z )= or -N=, R ^Z is hydrogen or a substituent,

X is ^each independently a single bond, > _NR ^NX , > ^O , >C ( _-R ^C It is substituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CX and R ^IX are each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted. It is substituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and two R ^CX may be bonded to each other to form a ring, and two R ^IX may be bonded to each other to form a ring. R ^NX , R ^CX and R ^IX may each be bonded to one or two rings to which X containing itself is bonded,

At least one selected from the group consisting of an aryl ring and a heteroaryl ring in the formula (Int) may be condensed with at least one cycloalkane, and the cycloalkane may be substituted with at least one substituent. At least one -CH ₂ - in the cycloalkane may be substituted with -O-,

At least one hydrogen in the formula (Int) may be substituted with cyano, halogen, or deuterium.

<20> A compound represented by the formula (Int);

In the expression (Int),

Ring B, ring C, ring D, ring E, ring F, ring G, ring H, and ring I are each independently a substituted or unsubstituted aryl ring or a substituted or unsubstituted heteroaryl ring,

The broken line connecting the C ring and the D ring indicates that the C ring and the D ring are not bonded at the position of the dashed line, or are bonded through a single bond or linking group at the position of the broken line,

Z is -C(-R ^Z )= or -N=, R ^Z is hydrogen or a substituent,

X is ^each independently a single bond, > _NR ^NX , > ^O , >C ( _-R ^C It is substituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CX and R ^IX are each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted. It is substituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and two R ^CX may be bonded to each other to form a ring, and two R ^IX may be bonded to each other to form a ring. R ^NX , R ^CX and R ^IX may each be bonded to one or two rings to which X containing itself is bonded,

At least one selected from the group consisting of an aryl ring and a heteroaryl ring in the formula (Int) may be condensed with at least one cycloalkane, and the cycloalkane may be substituted with at least one substituent. At least one -CH ₂ - in the cycloalkane may be substituted with -O-,

At least one hydrogen in the formula (Int) may be substituted with cyano, halogen, or deuterium.

According to the present invention, a novel polyaromatic compound useful as a material for organic devices such as organic electroluminescent elements is provided. The polycyclic aromatic compound of the present invention can be used in the production of organic devices such as organic electroluminescent elements.

1 is a schematic cross-sectional view showing an example of an organic electroluminescent device.
Figure 2 is an energy level diagram showing the energy relationship between the host, assisting dopant, and emitting dopant of a TAF device using a general fluorescent dopant.
Figure 3 is an energy level diagram showing an example of the energy relationship between the host, assisting dopant, and emitting dopant in the organic electroluminescent device of one aspect of the present invention.

Below, the present invention is explained in detail. The description of the structural requirements described below may be based on representative embodiments or specific examples, but the present invention is not limited to such embodiments. In addition, in this specification, the numerical range indicated using “~” means a range that includes the numerical values written before and after “~” as the lower limit and upper limit. In addition, in this specification, “hydrogen” in the description of the structural formula means “hydrogen atom (H).” Similarly, “carbon atom (C)” is sometimes referred to as “carbon.”

In this specification, “adjacent groups” means two groups each bonded to two adjacent atoms (two atoms directly bonded by a covalent bond) in the structural formula.

In this specification, “Me” is methyl, “Et” is ethyl, “nBu” is n-butyl (normal butyl), “tBu” is t-butyl (tertiary butyl), “iBu” is isobutyl, and “secBu” is " is secondaryributyl, "nPr" is n-propyl (normal propyl), "iPr" is isopropyl, "tAm" is t-amyl, "2EH" is 2-ethylhexyl, "tOct" is t-octyl, " “Ph” is phenyl, “Mes” is mesityl (2,4,6-trimethylphenyl), “Ad” is 1-adamantyl, “Tf” is trifluoromethanesulfonyl, “TMS” is trimethylsilyl, “D” represents deuterium.

In this specification, the organic electroluminescent device is sometimes referred to as an organic EL device.

In this specification, the chemical structure or substituent is expressed in terms of carbon number, but in the case where the chemical structure is substituted by a substituent or when the substituent is further substituted by a substituent, the number of carbon atoms refers to the number of carbon atoms in the chemical structure or each substituent, It does not mean the total carbon number of the chemical structure and substituents, or the total carbon number of substituents and substituents. For example, “substituent B of carbon number Y substituted by substituent A of carbon number X” means that “substituent A of carbon number It is not the total number of carbons in B. Also, for example, “substituent B of carbon number Y substituted by substituent A” means that “substituent A (with no limitation on carbon number)” replaces “substituent B of carbon number Y”, and carbon number Y is substituent A and It is not the total carbon number of substituent B.

0. Description of rings and substituents

First, details of the rings and substituents used in this specification will be described below.

The "aryl ring" in the present specification includes, for example, an aryl ring having 6 to 30 carbon atoms, an aryl ring having 6 to 16 carbon atoms is preferable, an aryl ring having 6 to 12 carbon atoms is more preferable, and an aryl ring having 6 to 12 carbon atoms is more preferable. An aryl ring of ~10 is particularly preferred.

Specific examples of “aryl rings” include monocyclic benzene rings, bicyclic biphenyl rings, condensed bicyclic naphthalene rings, indene rings, and tricyclic terphenyl rings (m-terphenyl, o-terphenyl, p-terphenyl). ), acenaphthylene ring, fluorene ring, phenalene ring, phenanthrene ring, anthracene ring, condensed 3-ring system, triphenylene ring, pyrene ring, naphthacene ring, chrysene ring, fused 5-ring system, perylene ring, Pentacene pills, etc. can be mentioned. Additionally, the fluorene ring, benzofluorene ring, and indene ring also include structures in which a fluorene ring, a benzofluorene ring, and a cyclopentane ring are spiro-bonded, respectively. In addition, in the fluorene ring, benzofluorene ring, and indene ring, two of the two hydrogens of methylene in the structure are each substituted with an alkyl such as methyl as the first substituent described later, resulting in dimethylfluorene ring and dimethylbenzofluorene. Rings, dimethylindene rings, etc. are also included.

Examples of the “heteroaryl ring” in this specification include heteroaryl rings having 2 to 30 carbon atoms, with heteroaryl rings having 2 to 25 carbon atoms being preferable, and heteroaryl rings having 2 to 20 carbon atoms being more preferable. And, a heteroaryl ring having 2 to 15 carbon atoms is more preferable, and a heteroaryl ring having 2 to 10 carbon atoms is particularly preferable. Examples of the “heteroaryl ring” include heterocycles containing 1 to 5 heteroatoms selected from oxygen, sulfur, nitrogen, selenium, phosphorus, and tellurium in addition to carbon as ring atoms.

Specific "heteroaryl rings" include, for example, pyrrole ring, oxazole ring, isoxazole ring, thiazole ring, isothiazole ring, imidazole ring, oxadiazole ring (furazane ring, etc.), thiadiazole ring, triazole ring, tetra. Sol ring, pyrazole ring, pyridine ring, pyrimidine ring, pyridazine ring, pyrazine ring, triazine ring, indole ring, isoindole ring, 1H-indazole ring, benzoimidazole ring, benzopyrrole ring, benzoxazole ring, benzothiazole ring. , 1H-benzotriazole ring, quinoline ring, isoquinoline ring, cinnoline ring, quinazoline ring, quinoxaline ring, phthalazine ring, naphthyridine ring, purine ring, pteridine ring, carbazole ring, acridine ring, pe Noxathiazine ring, phenoxazine ring, benzooxazinophenoxazine ring, phenothiazine ring, phenazine ring, phenazacillin ring, indolizine ring, furan ring, benzofuran ring, isobenzofuran ring, dibenzofuran ring, thiophene Ring, benzothiophene ring, dibenzothiophene ring, thiantrene ring, indolocarbazole ring, benzoindolocarbazole ring, dibenzoindolocarbazole ring, naphthobenzofuran ring, dioxine ring, dihydroa Cridine ring, xanthene ring, thioxanthene ring, dibenzodioxine ring, dioxaboranaphthoanthracene ring (5,9-dioxa-13b-bora-13bH-naphtho[3,2,1-de]anthracene ring etc.), benzoselenophen pill, etc. are mentioned. In addition, in the dihydroacridine ring, xanthene ring, and thioxanthene ring, two of the two hydrogens of methylene in the structure are each substituted with an alkyl such as methyl as the first substituent described later, and dimethyldihydroacridine ring, dimethylxanthene ring, It is also preferable that it is made of a dimethylthioxanthene ring or the like. Additionally, dicyclic bipyridine rings, phenylpyridine rings, and pyridylphenyl rings, and tricyclic terpyridine rings, bispyridylphenyl rings, and pyridylbiphenyl rings, can also be cited as “heteroaryl rings.” In addition, “heteroaryl ring” shall also include pyran ring.

In this specification, the substituent may be substituted with another substituent. For example, a specific substituent may be described as “substituted or unsubstituted.” This means that the specific substituent is substituted with at least one other substituent, or is not substituted. In the same sense, there are cases where it is said, “It may be substituted.” In this specification, the specific substituent at this time may be referred to as a “first substituent”, and the other substituent may be referred to as a “second substituent”.

In this specification, substituent group Z is,

Aryl, which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl, and cycloalkyl,

Heteroaryl, which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl, and cycloalkyl,

Diarylamino, which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl, and cycloalkyl (two aryls may be bonded to each other through a linking group),

Diheteroarylamino, which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl, and cycloalkyl (two heteroaryls may be bonded to each other through a linking group),

Arylheteroarylamino, which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl, and cycloalkyl (aryl and heteroaryl may be bonded to each other through a linking group),

Diarylboryl, which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl, and cycloalkyl (two aryls may be bonded through a single bond or linking group),

Alkyl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl and cycloalkyl,

Cycloalkyl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl,

Alkoxy, which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, and cycloalkyl,

Aryloxy, which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl, and cycloalkyl, and

It is made from substituted silyl.

Aryl, which is the second substituent in each group of substituent group Z, may be further substituted with aryl, heteroaryl, alkyl, or cycloalkyl. Similarly, heteroaryl, which is the second substituent, may be substituted with aryl, heteroaryl, alkyl, or cycloalkyl. It may be substituted with alkyl.

In this specification, when referring to a “substituent”, unless there is a separate explanation (for example, a separate explanation regarding substituents such as an aryl ring in the A ring, etc. or R ^Z ), it refers to a substituent group selected from the substituent group Z. Any one type will do. For example, when a group described as “substituted or unsubstituted” is substituted, the group may be substituted with at least one group selected from the substituent group Z.

In this specification, “aryl” refers to, for example, aryl with 6 to 30 carbon atoms, preferably, aryl with 6 to 20 carbon atoms, aryl with 6 to 16 carbon atoms, aryl with 6 to 12 carbon atoms, or aryl with 6 to 12 carbon atoms. Aryl of 10, etc.

The specific “aryl” is. Monovalent groups of the above-mentioned “aryl ring” include, for example, monocyclic phenyl, bicyclic biphenylyl (2-biphenylyl, 3-biphenylyl, or 4-biphenylyl), condensation dicyclic naphthyl (1-naphthyl or 2-naphthyl), tricyclic terphenylyl (m-terphenyl-2'-yl, m-terphenyl-4'-yl, m-terphenyl-5) '-yl, o-terphenyl-3'-yl, o-terphenyl-4'-yl, p-terphenyl-2'-yl, m-terphenyl-2-yl, m-terphenyl-3- 1, m-terphenyl-4-yl, o-terphenyl-2-yl, o-terphenyl-3-yl, o-terphenyl-4-yl, p-terphenyl-2-yl, p-ter phenyl-3-yl, or p-terphenyl-4-yl), condensed tricyclic, acenaphthylene-(1-, 3-, 4-, or 5-)yl, fluorene-(1-, 2) -, 3-, 4-, or 9-) days, phenalen-(1- or 2-) days, phenanthrene-(1-, 2-, 3-, 4-, or 9-) days, or anthracene -(1-, 2-, or 9-)yl, tetracyclic tetraphenylyl (5'-phenyl-m-terphenyl-2-yl, 5'-phenyl-m-terphenyl-3-yl, 5 '-phenyl-m-terphenyl-4-yl, or m-quarterphenyl), condensed tetracyclic, triphenylen-(1- or 2-)yl, pyrene-(1-, 2-, or 4- ) yl, or naphthacene-(1-, 2-, or 5-)yl, or, which is a condensed pentacyclic system, perylene-(1-, 2-, or 3-)yl, or pentacene-(1- , 2-, 5-, or 6-) days, etc. In addition, the monovalent group of spirofluorene, etc. can be mentioned.

In addition, the aryl as the second substituent includes aryl such as phenyl (specific examples are groups described above), alkyl such as methyl (specific examples are groups described later), and cycloalkyl such as cyclohexyl or adamantyl. Structures substituted with at least one group selected from the group consisting of (groups of which specific examples will be described later) are also included.

As an example, a group in which the 9th position of fluorenyl as the second substituent is substituted with aryl such as phenyl, alkyl such as methyl, or cycloalkyl such as cyclohexyl or adamantyl.

“Arylene” is, for example, arylene with 6 to 30 carbon atoms, preferably arylene with 6 to 20 carbon atoms, arylene with 6 to 16 carbon atoms, arylene with 6 to 12 carbon atoms, or arylene with 6 to 12 carbon atoms. Arylene of 10, etc.

Specific examples of “arylene” include a divalent group obtained by removing one hydrogen from the above-mentioned “aryl” (monovalent group).

“Heteroaryl” is, for example, heteroaryl with 2 to 30 carbon atoms, preferably heteroaryl with 2 to 25 carbon atoms, heteroaryl with 2 to 20 carbon atoms, heteroaryl with 2 to 15 carbon atoms, or 2 to 2 carbon atoms. 10 heteroaryl, etc. “Heteroaryl” contains one or more heteroatoms selected from oxygen, sulfur, nitrogen, etc. in addition to carbon as ring atoms, preferably 1 to 5 heteroatoms.

Specific examples of “heteroaryl” include the monovalent group of the “heteroaryl ring” described above, for example, pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, imidazolyl, and oxadiazolyl. , thiadiazolyl, triazolyl, tetrazolyl, pyrazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, indolyl, isoindolyl, 1H-indazolyl, benzoimidazolyl, benzoxa. Zolyl, benzothiazolyl, 1H-benzotriazolyl, quinolinyl, isoquinolinyl, cinnolinyl, quinazolinyl, quinoxalinyl, phenanthrolinyl, phthalazinyl, naphthyridinyl, purinyl, pteri. Dinyl, carbazolyl, acridinyl, phenoxathiinyl, phenoxazinyl, phenothiazinyl, phenazinyl, phenazoxylinyl, indolizinyl, furanyl, benzofuranyl, isobenzofuranyl, dibenzofuranyl. Nyl, naphthobenzofuranyl, thienyl, benzothienyl, isobenzothienyl, dibenzothienyl, naphthobenzothienyl, benzophosphoryl, dibenzophosphoryl, benzophosphoryl oxide ring monovalent group, di Monovalent groups of the benzophosphole oxide ring, furazanyl, thianthrenyl, indolocarbazolyl, benzoindolocarbazolyl, dibenzoindolocarbazolyl, imidazolinyl, or oxazolinyl, etc. there is. In addition, the monovalent group of spiro[fluorene-9,9'-xanthene], the monovalent group of spirobi[silafluorene], and the monovalent group of benzoselenophene can be mentioned.

In addition, heteroaryl as the second substituent includes aryl such as phenyl (specific examples are groups described above), alkyl such as methyl (specific examples are groups described later), and cyclo such as cyclohexyl or adamantyl. Structures substituted with at least one group selected from the group consisting of alkyl (a group whose specific examples will be described later) are also included.

As an example, a group in which the 9th position of carbazolyl as the second substituent is substituted with aryl such as phenyl, alkyl such as methyl, or cycloalkyl such as cyclohexyl or adamantyl. In addition, nitrogen-containing heteroaryls such as pyridyl, pyrimidinyl, triazinyl, and carbazolyl, which are further substituted with phenyl or biphenylyl, are also included in heteroaryl as the second substituent.

“Heteroarylene” is, for example, heteroarylene having 2 to 30 carbon atoms, preferably heteroarylene having 2 to 25 carbon atoms, heteroarylene having 2 to 20 carbon atoms, heteroarylene having 2 to 15 carbon atoms. , or heteroarylene having 2 to 10 carbon atoms, etc. In addition, “heteroarylene” is, for example, a divalent group such as a heterocycle containing 1 to 5 heteroatoms selected from oxygen, sulfur, and nitrogen in addition to carbon as ring atoms.

Specific examples of “heteroarylene” include a divalent group obtained by removing one hydrogen from the above-mentioned “heteroaryl” (monovalent group).

“Diarylamino” is amino in which two aryls are substituted, and the description of “aryl” described above can be cited for details on this aryl.

“Diheteroarylamino” is an amino group in which two heteroaryls are substituted, and the description of “heteroaryl” described above can be cited for details on this heteroaryl.

“Arylheteroarylamino” is an amino group in which aryl and heteroaryl are substituted. For details on aryl and heteroaryl, the explanation of “aryl” and “heteroaryl” described above can be cited.

Two aryls in diarylamino as the first substituent may be bonded to each other through a linking group, and two heteroaryls in diheteroarylamino as the first substituent may be bonded to each other through a linking group, and the first substituent may be bonded to each other through a linking group. Aryl and heteroaryl of arylheteroarylamino as substituents may be bonded to each other through a linking group. Here, the description of “bonding through a linking group” indicates that, for example, two phenyls of diphenylamino form a bond through a linking group, as shown below. This description also applies to diheteroarylamino and arylheteroarylamino, formed from aryl or heteroaryl.

(* indicates binding position)

^As a _linking group _, ^specifically , ^{> O} , > ^NR >CO, >CS, >SO, >SO ₂ , and >Se. ^{R In} _addition ^{, two R} _{_} ^_ They may be combined with each other through ^Y to form a ring. X ^Y includes >O, >NR ^Y , >C(-R ^Y ) ₂ , >Si(-R ^Y ) ₂ , >S, >CO, >CS, >SO, >SO ₂ , and >Se. and R ^Y is each independently alkyl, cycloalkyl, aryl, or heteroaryl, and these may be substituted with alkyl, cycloalkyl, aryl, or heteroaryl. ^{However ,} _{in the} ^{case where} Furthermore, alkenylene can also be mentioned as a linking group. Any hydrogen of the alkenylene may each independently be substituted with ^{R 2} It may be substituted. ^{The two R} do. That is ^, -C( ^-R

In addition, in this specification, when it is simply described as “diarylamino”, “diheteroarylamino” or “arylheteroarylamino”, unless specifically limited, “two aryls of diarylamino are linked to each other.” may be bonded through”, “The two heteroaryls of the above diheteroarylamino may be bonded to each other through a linking group,” and “The aryl and heteroaryl of the above arylheteroarylamino may be bonded to each other through a linking group. It is assumed that the explanation “” is added.

“Diarylboryl” is a boryl in which two aryls are substituted, and the description of “aryl” described above can be cited for details on this aryl. Additionally, these two aryls are single bonds or linking groups (e.g. -CH=CH-, -CR=CR-, -C≡C-, >NR, >O, >S, >C(-R) ₂ , >Si(-R) ₂ , or >Se) may be bonded. Here, R of -CR=CR-, R of >NR, R of >C(-R) ₂ , and R of >Si(-R) are aryl, heteroaryl, diarylamino, alkyl, alkenyl. , alkynyl, cycloalkyl, alkoxy, or aryloxy, and at least one hydrogen in R may be further substituted with aryl, heteroaryl, alkyl, alkenyl, alkynyl, or cycloalkyl. Additionally, two adjacent R groups may combine to form a ring, forming cycloalkylene, arylene, and heteroarylene. Details of the substituents listed here include the description of “aryl”, “arylene”, “heteroaryl”, “heteroarylene”, and “diarylamino” described above, and “alkyl” and “alkyl” described later. The descriptions of “kenyl”, “alkynyl”, “cycloalkyl”, “cycloalkylene”, “alkoxy”, and “aryloxy” may be cited. Additionally, in the case where "diarylboryl" is simply described in this specification, unless specifically limited, an explanation is added that "the two aryls of diarylboryl may be bonded to each other through a single bond or a linking group." Pretend it exists.

“Alkyl” may be either straight chain or branched chain, for example, straight chain alkyl with 1 to 24 carbon atoms or branched chain alkyl with 3 to 24 carbon atoms, preferably alkyl with 1 to 18 carbon atoms (3 to 2 carbon atoms). Branched chain alkyl with 18 carbon atoms), Alkyl with 1 to 12 carbon atoms (branched chain alkyl with 3 to 12 carbon atoms), Alkyl with 1 to 6 carbon atoms (branched chain alkyl with 3 to 6 carbon atoms), Alkyl with 1 to 5 carbon atoms (3 carbon atoms) branched chain alkyl of ~5), alkyl of 1 to 4 carbon atoms (branched chain alkyl of 3 to 4 carbon atoms), etc.

Specific “alkyl” includes, for example, methyl, ethyl, n-propyl, isopropyl, 1-ethyl-1-methylpropyl, 1,1-diethylpropyl, 1,1,2-trimethylpropyl, 1,1 ,2,2-tetramethylpropyl, 1-ethyl-1,2,2-trimethylpropyl, n-butyl, isobutyl, s-butyl, t-butyl, 2-ethylbutyl, 1,1-dimethylbutyl, 3 ,3-dimethylbutyl, 1,1-diethylbutyl, 1-ethyl-1-methylbutyl, 1-propyl-1-methylbutyl, 1,1,3-trimethylbutyl, 1-ethyl-1,3-dimethyl Butyl, n-pentyl, isopentyl, neopentyl, t-pentyl (t-amyl), 1-methylpentyl, 2-propylpentyl, 1,1-dimethylpentyl, 1-ethyl-1-methylpentyl, 1-propyl -1-methylpentyl, 1-butyl-1-methylpentyl, 1,1,4-trimethylpentyl, n-hexyl, 1-methylhexyl, 2-ethylhexyl, 1,1-dimethylhexyl, 1-ethyl-1 -Methylhexyl, 1,1,5-trimethylhexyl, 3,5,5-trimethylhexyl, n-heptyl, 1-methyl heptyl, 1-hexylheptyl, 1,1-dimethylheptyl, 2,2-dimethylheptyl, 2,6-dimethyl-4-heptyl, n-octyl, t-octyl (1,1,3,3-tetramethylbutyl), 1,1-dimethyloctyl, n-nonyl, n-decyl, 1-methyldecyl , n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, or n-eicosyl.

“Alkylene” is a divalent group obtained by removing the hydrogen of any one of “alkyl”, for example, methylene, ethylene, and propylene.

Regarding "alkenyl", the explanation of "alkyl" mentioned above can be referred to. It is a group in which the C-C single bond in the structure of "alkyl" is replaced with a C=C double bond, and it has not only one but two or more single bonds. Also includes groups where the bond is replaced by a double bond (also called alkadiene-yl or alkatrien-yl).

“Alkenylene” is a divalent group obtained by removing any hydrogen of “alkenyl”, and examples include vinylene.

Regarding "alkynyl", the explanation of "alkyl" mentioned above can be referred to. It is a group in which the C-C single bond in the structure of "alkyl" is replaced with a C≡C triple bond, and it has not only one but two or more single bonds. Also includes groups where the bond is replaced by a triple bond (also called alkadiin-yl or alkatrien-yl).

“Cycloalkyl” is, for example, cycloalkyl with 3 to 24 carbon atoms, preferably cycloalkyl with 3 to 20 carbon atoms, cycloalkyl with 3 to 16 carbon atoms, cycloalkyl with 3 to 14 carbon atoms, and 3 to 12 carbon atoms. cycloalkyl, cycloalkyl with 5 to 10 carbon atoms, cycloalkyl with 5 to 8 carbon atoms, cycloalkyl with 5 to 6 carbon atoms, or cycloalkyl with 5 carbon atoms, etc.

Specific “cycloalkyl” includes, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, or alkyl of these with 1 to 5 carbon atoms or 1 to 4 carbon atoms (especially methyl) substituent, bicyclo[1.1.0]butyl, bicyclo[1.1.1]pentyl, bicyclo[2.1.0]pentyl, bicyclo[2.1.1]hexyl, bicyclo[3.1.0]hexyl, Cyclo[2.2.1]heptyl (norbornyl), bicyclo[2.2.2]octyl, adamantyl, diamantyl, decahydronaphtharenyl, or decahydroazulenyl.

“Cycloalkylene” is, for example, cycloalkylene with 3 to 24 carbon atoms, preferably cycloalkylene with 3 to 20 carbon atoms, cycloalkylene with 3 to 16 carbon atoms, and cycloalkylene with 3 to 14 carbon atoms. , cycloalkylene with 3 to 12 carbon atoms, cycloalkylene with 5 to 10 carbon atoms, cycloalkylene with 5 to 8 carbon atoms, cycloalkylene with 5 to 6 carbon atoms, or cycloalkylene with 5 carbon atoms, etc.

Specific examples of “cycloalkylene” include structures in which one hydrogen is removed from the above-mentioned “cycloalkyl” (monovalent group) to form a divalent group.

“Cycloalkenyl” is a group having a structure in which the single bond between two carbons of at least one group in the above-mentioned “cycloalkyl” is a double bond (for example, -CH ₂ -CH ₂ - is - CH=CH-substituted group) and groups that do not correspond to aryl can be mentioned. Specifically, 1-cyclohexenyl, 1-cyclopentenyl, etc. can be mentioned.

“Alkoxy” is a group represented by “Alk-O- (Alk is alkyl),” and the above-mentioned explanation of “alkyl” can be cited for details on this alkyl.

“Aryloxy” is a group represented by “Ar-O- (Ar is aryl),” and the description of “aryl” described above can be cited for details on this aryl.

“Substituted silyl” is, for example, silyl substituted with at least one of aryl, alkyl, and cycloalkyl, and is preferably triarylsilyl, trialkylsilyl, tricycloalkylsilyl, dialkylcycloalkylsilyl, or alkyl. It is dicycloalkylsilyl.

“Triarylsilyl” is a silyl group substituted with three aryls, and the description of “aryl” described above can be cited for details on this aryl.

Specific “triarylsilyl” includes, for example, triphenylsilyl, diphenylmononaphthylsilyl, monophenyldinaphthylsilyl, or trinaphthylsilyl.

“Trialkylsilyl” is a silyl group substituted with three alkyls, and the description of “alkyl” described above can be cited for details on this alkyl.

Specific “trialkylsilyl” includes, for example, trimethylsilyl, triethylsilyl, trin-propylsilyl, triisopropylsilyl, trin-butylsilyl, triisobutylsilyl, tris-butylsilyl, trit- Butylsilyl, ethyldimethylsilyl, n-propyldimethylsilyl, isopropyldimethylsilyl, n-butyldimethylsilyl, isobutyldimethylsilyl, s-butyldimethylsilyl, t-butyldimethylsilyl, methyldiethylsilyl, n-propyldi. Ethylsilyl, isopropyldiethylsilyl, n-butyldiethylsilyl, s-butyldiethylsilyl, t-butyldiethylsilyl, methyl din-propylsilyl, ethyl din-propylsilyl, n-butyl din- Propylsilyl, s-butyldin-propylsilyl, t-butyldin-propylsilyl, methylisopropylsilyl, ethyldiisopropylsilyl, n-butyldiisopropylsilyl, s-butyldiisopropylsilyl, or t -Butyldiisopropylsilyl, etc.

“Tricycloalkylsilyl” is a silyl group substituted with three cycloalkyls, and the description of “cycloalkyl” described above can be cited for details on this cycloalkyl.

Specific “tricycloalkylsilyl” includes, for example, tricyclopentylsilyl or tricyclohexylsilyl.

“Dialkylcycloalkylsilyl” is a silyl group substituted with two alkyls and one cycloalkyl, and the description of “alkyl” and “cycloalkyl” above can be referred to for details of this alkyl and cycloalkyl. .

“Alkyldicycloalkylsilyl” is a silyl group substituted with one alkyl and two cycloalkyl, and the description of “alkyl” and “cycloalkyl” mentioned above can be cited for details of this alkyl and cycloalkyl. .

<When two groups bonded to the same atom bond to each other>

In this specification, when two groups bonded to the same atom may be bonded to each other to form a ring, they may be bonded by a single bond or a linking group (together, they are also called a linking group), and the linking group may be -CH ₂ - CH ₂ -, -CHR-CHR-, -CR ₂ -CR ₂ -, -CH=CH-, -CR=CR-, -C≡C-, -N(-R)-, -O-, -S -, -C(-R) ₂ -, -Si(-R) ₂ -, or -Se- can be mentioned, and examples include the following structures. In addition, R of -CHR-CHR-, R of -CR ₂ -CR ₂ -, R of -CR=CR-, R of -N(-R)-, R of -C(-R) ₂ -, and R of -Si(-R) ₂ - are each independently hydrogen, aryl optionally substituted with alkyl or cycloalkyl, heteroaryl optionally substituted with alkyl or cycloalkyl, or alkyl optionally substituted with cycloalkyl. , alkenyl which may be substituted with alkyl or cycloalkyl, alkynyl which may be substituted with alkyl or cycloalkyl, or cycloalkyl which may be substituted with alkyl or cycloalkyl. Additionally, two adjacent R groups may combine to form a ring to form cycloalkylene, arylene, or heteroarylene.

As a linking group, a single bond, -CR=CR-, -N(-R)-, -O-, -S-, -C(-R) ₂ -, -Si(-R) ₂ -, and - as a linking group. Se- is preferred, a single bond, -CR=CR-, -N(-R)-, -O-, -S-, and -C(-R) ₂ - as a linking group are more preferred, a single bond, -CR=CR-, -N(-R)-, -O-, and -S- as linking groups are more preferable, and a single bond is most preferable.

The position where two R are bonded by the linking group is not particularly limited as long as it is a position where bonding is possible, but it is preferable to bond at the most adjacent position. For example, when the two groups are phenyl, "C" in phenyl or It is preferable to bond at ortho (second position) positions based on the bonding position (first position) of “Si” (refer to the structural formula above).

One. polycyclic aromatic compound

<Description of the overall structure of the compound>

The polycyclic aromatic compound of the present invention has a structure containing a structural unit represented by formula (1) or formula (2).

In formulas (1) and (2), rings B to I are each independently a substituted or unsubstituted aryl ring or a substituted or unsubstituted heteroaryl ring.

A polycyclic aromatic compound having a structure containing a structural unit represented by formula (1) preferably has a structure represented by any one formula selected from the group consisting of the following formulas (1-a) to (1-l): It is a compound that has . In addition, the polycyclic aromatic compound having a structure containing a structural unit represented by formula (2) preferably has a structure represented by any one formula selected from the group consisting of formulas (2-a) to formulas (2-l). It is a compound that has . In that sense, each ring in each formula is represented by lowercase letters “b”, “c”, “d”, “e”, “f”, “g”, “h”, and “i”.

The definitions and preferred ranges of the symbols in each of the above formulas will be described later.

Polycyclic aromatic compounds having a structure containing a structural unit expressed by formula (1) or formula (2) have a structure in which aromatic rings are connected to hetero elements such as boron, nitrogen, oxygen, and sulfur, and have a large HOMO-LUMO It has a gap (band gap Eg in a thin film). This is because the six-membered ring containing a hetero element has low aromaticity, and the reduction of the HOMO-LUMO gap due to expansion of the conjugate system is suppressed. In polycyclic aromatic compounds having a structure containing a structural unit represented by Formula (1) or Formula (2), the HOMO-LUMO gap can be arbitrarily changed depending on the type of hetero element and connection method. This is thought to be due to the fact that the energy of HOMO and LUMO can be moved arbitrarily depending on the spatial spread and energy of the coorbital or lone pair of the hetero element. For example, a polycyclic aromatic compound having a structure containing a structural unit represented by formula (1) or formula (2), where Y is B (boron), is compared to a polycyclic aromatic compound with less B (Y). Green light is emitted when the LUMO is deep or the band gap Eg is narrowed.

In these polyaromatic compounds, the excited state SOMO1 and SOMO2 are localized on each atom due to electronic perturbation of the hetero element, so the half width of the fluorescence emission peak is narrow, and when used as a dopant in an organic EL device, they emit light with high color purity. This is obtained. For the same reason, ΔE _S1T1 becomes small, showing thermally activated delayed fluorescence, and high efficiency can be obtained when used as an emitting dopant in organic EL devices.

Moreover, since the energy of HOMO and LUMO can be arbitrarily moved by introducing a substituent, it is possible to optimize the ionization potential and electron affinity depending on the surrounding material. However, the present invention is not particularly limited to this principle.

<Explanation of ring structure in compounds>

In each of equations (1) and (2), “B”, “C”, “D”, “E”, “F”, “G”, “H”, and “I” within the circle are each circle. It is a symbol representing the ring structure represented by . The structure represented by formula (1) or formula (2) consists of at least nine aromatic rings as a ring, B ring, C ring, D ring, E ring, F ring, G ring, H ring, and I ring being boron. , it has a structure where a ring structure is formed by connecting with hetero elements such as oxygen, nitrogen, and sulfur. The formed ring structure is a condensed ring structure composed of at least 17 rings in formula (1) and 19 rings in formula (2).

In each of formulas (1) and (2), ring B, ring C, ring D, ring E, ring F, ring G, ring H, and ring I are each independently a substituted or unsubstituted aryl ring or It is a substituted or unsubstituted heteroaryl ring. A substituted or unsubstituted aryl ring in the B ring, C ring, D ring, E ring, F ring, G ring, H ring, and I ring of the structures represented by formula (1) and formula (2), respectively, or In a substituted or unsubstituted heteroaryl ring, the substituent when saying “substituted or unsubstituted (substituted or unsubstituted)” is from the group obtained by adding a substituent expressed by the formula (A30) described later to the substituent group Z. At least one substituent may be selected. Additionally, the substituent may be substituted or unsubstituted diarylphosphino such as diphenylphosphino. For the preferable range of the substituent, refer to the preferable range of R ^Z described later. When a plurality of substituents exist, the plurality of substituents may be the same or different from each other.

In each of Formulas (1) and (2), the broken line connecting the C ring and the D ring indicates that the C ring and the D ring are not bonded at the position of the broken line, or are bonded through a single bond or linking group at the position of the broken line. indicates. When bonded through a single bond or linking group at the position of the broken line in formulas (1) and (2), the single bond or linking group may be indicated as “L”. When the C ring and the D ring are bonded through a linking group, the linking group may include >NR ^NL , >O, >C(-R ^CL ) ₂ , >S, or >Se. R ^NL is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CL is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and two R ^CL may be bonded to each other to form a ring, and R ^NL and R ^CL each include themselves. The linking group may be bonded to one or two or more of Z bonded to the carbon atom to which it is bonded. It is preferable that the C ring and the D ring are bonded through a single bond at the position indicated by the broken line, or are not bonded at the position indicated by the broken line.

The B ring and E ring in formula (1) and formula (2) each form a trivalent group having a bond at three consecutive carbons in the ring of the aryl ring or heteroaryl ring in the structure. These three binding hands bind to N and two Y, respectively. Among the B ring and E ring, the ring containing carbon having the above three bonding elements as a ring element is preferably a 5-membered ring or a 6-membered ring, and more preferably a 6-membered ring. This ring may be further condensed with another ring. Examples of 6-membered rings include benzene rings, pyridine rings, pyrazine rings, and pyrimidine rings. Examples of a 6-membered ring further condensed with another ring include a naphthalene ring, a quinoline ring, a dibenzofuran ring, a dibenzothiophene ring, and a carbazole ring. Examples of 5-membered rings include furan rings, thiophene rings, pyrrole rings, and thiazole rings. Examples of a 5-membered ring further condensed with another ring include a benzofuran ring, a benzothiophene ring, and an indole ring.

The F ring and G ring in formula (1) may each form a trivalent group having a bond at three consecutive carbon atoms in the ring of the aryl ring or heteroaryl ring in the structure. It binds to N, Y, and X, respectively, through these three binding hands. When the F ring and the G ring are bonded to R ^NX , R ^CX or R ^IX , they may be a tetravalent group. Among the F ring and G ring, the ring containing carbon having the above three bonding elements as a ring element is preferably a 5-membered ring or a 6-membered ring, and more preferably a 6-membered ring. This ring may be further condensed with another ring. Examples of 6-membered rings include benzene rings, pyridine rings, pyrazine rings, and pyrimidine rings. Examples of a 6-membered ring further condensed with another ring include a naphthalene ring, a quinoline ring, a dibenzofuran ring, a dibenzothiophene ring, and a carbazole ring. Examples of 5-membered rings include furan rings, thiophene rings, pyrrole rings, and thiazole rings. Examples of a 5-membered ring further condensed with another ring include a benzofuran ring, a benzothiophene ring, and an indole ring.

The F ring and G ring in formula (2) may each form a tetravalent group having a bond at four consecutive carbons in the ring of the aryl ring or heteroaryl ring in the structure. These four binding hands bind to N, two Y, and X, respectively. When the F ring and the G ring are bonded to R ^NX , R ^CX or R ^IX , they may be a pentavalent group. Among the F ring and G ring, the ring containing carbon having the above four bonding elements as a ring element is preferably a 6-membered ring. This ring may be further condensed with another ring. Examples of 6-membered rings include benzene rings, pyridine rings, pyrazine rings, and pyrimidine rings. Examples of a 6-membered ring further condensed with another ring include a naphthalene ring, a quinoline ring, a dibenzofuran ring, a dibenzothiophene ring, and a carbazole ring.

The C ring, D ring, H ring, and I ring in formula (1) and formula (2) each have bonding hands at two adjacent carbons in the ring of the aryl ring or heteroaryl ring in the structure. All you have to do is form a group. Ring C and D are each bonded to N and Y through the above two bonding hands, and ring H and I are bonded to Y and X through the above two bonding hands, respectively. When the C ring and the D ring are bonded to each other through L, each may be a trivalent group. When the H ring and the I ring are each further bonded to R ^NX , R ^CX or R ^IX , they may be a trivalent group. Among the C ring, D ring, H ring, and I ring, the ring containing carbon having the above two bonding hands as a ring member is preferably a 5-membered ring or a 6-membered ring, and more preferably a 6-membered ring. This ring may be further condensed with another ring. Examples of 6-membered rings include benzene rings, pyridine rings, pyrazine rings, and pyrimidine rings. Examples of a 6-membered ring further condensed with another ring include a naphthalene ring, a quinoline ring, a dibenzofuran ring, a dibenzothiophene ring, and a carbazole ring. Examples of 5-membered rings include furan rings, thiophene rings, pyrrole rings, and thiazole rings. Examples of a 5-membered ring further condensed with another ring include a benzofuran ring, a benzothiophene ring, and an indole ring.

Additionally, the F ring, G ring, H ring, and I ring may have a condensed ring in their structures, and each may have one bond to another cyclic atom in the condensed ring. For example, it may contain a benzoimidazole ring or a benzopyrrole ring, and may be bonded to either X or Y at one carbon of the benzene ring and to the other side at one carbon or nitrogen of the imidazole ring or pyrrole ring. . At this time, it is preferable that X is a single bond.

In formula (1), the preferred ring structures of ring B, ring C, ring D, ring E, ring F, ring G, ring H, and ring I are formulas (1-a) to (1-l), respectively. ) are represented as the b ring, c ring, d ring, e ring, f ring, g ring, h ring, and i ring. In formula (2), the preferred ring structures of ring B, ring C, ring D, ring E, ring F, ring G, ring H, and ring I are formulas (2-a) to (2-l), respectively. ) are represented as the b ring, c ring, d ring, e ring, f ring, g ring, h ring, and i ring.

<Explanation of Z>

Z in the a ring of formulas (1) and (2) is -C(-R ^Z )= or -N=, respectively. R ^Z is each independently hydrogen or a substituent. The substituent includes at least one substituent selected from the group of substituent group Z plus a substituent represented by the formula (A30) described later, unsubstituted alkyl is preferable, and methyl is more preferable. R ^Z is preferably hydrogen. As Z in ring a, -C(-H)= or -N= is preferable, and -C(-H)= is more preferable.

Z in the a ring of formulas (1-a) to formula (1-l) and formulas (2-a) to formula (2-l) is the same as Z in the a ring of formulas (1) and (2). The meaning and desirable range are the same.

In formulas (1-a) to (1-l) and formulas (2-a) to (2-l), Z other than Z in ring a has the same meaning as Z in ring a, and is used as a substituent. , at least one substituent selected from the group of substituent group Z plus a substituent represented by the formula (A30) described later. Additionally, the substituent may be substituted or unsubstituted diarylphosphino such as diphenylphosphino. Preferred substituents include those described later as preferable substituents. Additionally, all adjacent Zs may have the following structures.

First, when all Zs in Z=Z are -C(-R ^Z )=, two R ^Z may be combined with each other to form an aryl ring or heteroaryl ring. The formed aryl ring or heteroaryl ring may each have a substituent. The substituent at this time includes at least one substituent selected from the group of substituent group Z plus a substituent represented by the formula (A30) described later. Additionally, the substituent may be substituted or unsubstituted diarylphosphino such as diphenylphosphino. The preferred range is the same as that of R ^Z. Additionally, Z=Z may each independently be >NR, >O, >C(-R) ₂ , >Si(-R) ₂ , >S, or >Se. At this time, R of >NR, >C(-R) ₂ and >Si(-R) ₂ is each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, or substituted or unsubstituted alkyl. , or substituted or unsubstituted cycloalkyl. The two R's of >C(-R) ₂ may be bonded to each other to form a ring, and the two R's of >Si(-R) ₂ may be bonded to each other to form a ring.

As an example of a structure containing four Z in each of Formulas (1-a) to Formula (1-l) and Formula (2-a) to Formula (2-l) and bonded to X and Y, indicates. Meanwhile, in the formulas below, R has the same meaning as R ^Z , but does not mean hydrogen and does not mean that R is bonded to each other. In addition, n is an integer of 0 to 4, and R ^N and R ^c are hydrogen, aryl which may be substituted with alkyl or cycloalkyl, heteroaryl which may be substituted with alkyl or cycloalkyl, and heteroaryl which may be substituted with cycloalkyl. It is alkyl or cycloalkyl which may be substituted with alkyl, and two R ^c may be bonded to each other to form a ring.

In each of the above partial structures, R is preferably alkyl, phenyl optionally substituted with alkyl, or a substituent represented by the formula (A30). n is preferably 0 or 1, and is more preferably 0.

Similar structural examples can be given for structures bonded to N and Y or structures containing three or two Zs.

In each a to i ring of formulas (1-a) to (1-l) and formulas (2-a) to formula (2-l), 0 to 2 Zs are -N= and the rest are It is preferable that it is -C(-R ^Z )=, it is more preferable that 0 to 1 are -N= and the rest are -C(-R ^Z )=, and it is even more preferable that all of them are -C(-R ^Z )=. do. In each equation, it is preferable that 0 to 8 Zs are -N= and the remainder is -C(-R ^Z )=, and 0 to 3 Zs are preferably -N= and the remainder are -C(-R ^Z )=. It is more preferable that 0 to 1 number is -N= and the remainder is -C(-R ^Z )=, and it is especially preferable that all of them are -C(-R ^Z )=. As any one of the substituents selected from the substituent group ^Z that is R desirable. As the substituent R ^Z , reference may also be made to the description of preferred substituents described later. In each formula, 0 to 3 R ^Z are preferably substituents, and the others are hydrogen. In particular, it is preferable that the substituent R ^Z is located at the para position of Y. In particular, it is preferable that the substituent R ^Z is located at the para position of B.

<Structure containing structural units expressed by formula (1) or formula (2)>

The polycyclic aromatic compound of the present invention is a polycyclic aromatic compound having a structure containing a structural unit represented by formula (1) or formula (2). Examples of polycyclic aromatic compounds having a structure containing the above structural units include polycyclic aromatic compounds represented by formula (1) or formula (2). Moreover, as a polycyclic aromatic compound having a structure containing the above structural unit, a form in which any ring (single or plural) contained in the above structural unit is bonded so that it is shared in a plurality of unit structures, and any ring contained in the above unit structure. A form in which the rings are combined by condensing each other can be mentioned. Additionally, any ring included in the above structural unit and the The unit structure may be a single bond or a plurality of bonds formed by linking groups such as alkylene, phenylene, or naphthylene having 1 to 3 carbon atoms. Among these, a form in which a plurality of rings are shared and bonded together is preferable.

<Explanation of L>

In formula (1-b), formula (1-d), formula (1-f), formula (2-b), formula (2-d), and formula (2-f), L is a single bond, >NR ^NL , >O, >C(-R ^CL ) ₂ , >S, or >Se. R ^NL is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CL is hydrogen, substituted or unsubstituted aryl, substituted Or it is unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and two R ^CL may be bonded to each other to form a ring, and R ^NL and R ^CL each contain themselves. It may be bonded to one or two or more of Z bonded to the carbon atom to which L is bonded. R ^NL is preferably aryl which may be substituted by alkyl or aryl, or heteroaryl which may be substituted by alkyl or aryl. R ^CL is preferably alkyl, and more preferably methyl. As L, a single bond is preferable.

<Description of X ^C >

Equation (1-c), Equation (1-d), Equation (1-e), Equation (1-f), Equation (1-g), Equation (1-h), Equation (1-i), Equation (1-j), Equation (1-k), Equation (1-l), Equation (2-c), Equation (2-d), Equation (2-e), Equation (2-f), Equation ( X ^C in 2-g), formula (2-h), formula (2-i), formula (2-j), formula (2-k), and formula (2-l) is each independently, >O, >NR, >C(-R) ² , >S, or >Se, where R of >NR is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted It is alkyl, substituted or unsubstituted cycloalkyl, and the R of >C(-R) ₂ is each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or It is a substituted or unsubstituted cycloalkyl, and >NR and >C(-R) ₂ may be bonded at R to one or two or more of Z bonded to the same carbon atom. X ^C is preferably >O or >S.

<Explanation of Y>

In each of equations (1) and (2), Y is independently >B-, >P-, >P(=O)-, >P(=S)-, >Al-, >Ga -, >As-, >C(-R ^Y )-, >Si(-R ^Y )-, or >Ge(-R ^Y )-. ^RY each independently represents optionally substituted aryl, optionally substituted heteroaryl, optionally substituted alkyl, or optionally substituted cycloalkyl. Y is each independently preferably >B-, >P-, >P(=O)-, or >P(=S)-, and more preferably all are >B-.

<Explanation of X>

^In each ^of Formulas _{( 1} ) and (2) ^, Or >Se. R ^NX is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CX and R ^IX are each independently hydrogen, It is substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and two R ^CX may be bonded to each other to form a ring, and two R ^IX may be bonded to each other to form a ring, and R ^NX , R ^CX and R ^IX may each be bonded to one or two rings to which X containing itself is bonded.

As X, it ^is each _{independently} ^preferably >NR ^N >R ^NX in NR ^NX is preferably substituted or unsubstituted aryl or substituted or unsubstituted heteroaryl, and is preferably substituted or unsubstituted phenyl. In a structure where all Y's are B, in order to obtain green light emission, ^it is preferable that at least one of the X's is >NR ^NX , and it is more preferable that all of the From the viewpoint of TADF properties, it is preferable that at least one is S.

<Explanation of changes in ring structure due to combination of X and ring>

R ^NX , R ^CX and R ^IX in Specifically, in formulas (1) and (2), R ^NX , R ^CX and R ^IX in R ^NX , R ^CX , and R ^IX in In formula (1B), R ^NX , R ^CX and R ^IX in may be bonded to the adjacent Z), and R ^NX , R ^CX and R ^IX in It may be bonded to Z) adjacent to the carbon to which is bonded.

When R ^NX , R ^CX and R ^IX are each bonded to a ring, the linking group is -CH ₂ -CH ₂ -, -CHR-CHR-, -CR ₂ -CR ₂ -, -CH=CH-, -CR=CR -, -C≡C-, -N(-R)-, -O-, -S-, -C(-R) ₂ -, -Si(-R) ₂ -, or -Se-, etc. there is. Among these, -CH=CH-, -CR=CR-, -N(-R)-, -O-, -S-, and -C(-R) ₂ - are preferred, -CH=CH-, -CR=CR-, -N(-R)-, -O-, and -S- are more preferred, and -CR=CR-, -N(-R)-, -O-, and -S- are more preferred. It is more desirable. R in “-CHR-CHR-” above, R in “-CR ₂ -CR ₂ -”, R in “-CR=CR-”, R in “-N(-R)-”, and “-C(-” R of “R) ₂ -” and R of “-Si(-R) ₂ -” are each independently hydrogen, aryl which may be substituted with alkyl or cycloalkyl, hetero which may be substituted with alkyl or cycloalkyl. alkyl which may be substituted by aryl, alkyl or cycloalkyl, alkenyl which may be substituted by alkyl or cycloalkyl, alkynyl which may be substituted by alkyl or cycloalkyl, or cycloalkyl which may be substituted by alkyl or cycloalkyl. . Additionally, two R's bonded to the same element may bond to form a ring. Furthermore, two adjacent R groups may be bonded to form a cycloalkylene ring, an arylene ring, and a heteroarylene ring. This ring may also be substituted with alkyl or cycloalkyl.

Examples of structures in which R ^NX , R ^CX and R ^IX are each bonded to a ring include compounds having a ring structure in which A compound having a ring structure represented by '-F) wherein X is contained in the condensed ring F' can be mentioned. Examples of the formed condensed ring include a carbazole ring, a phenoxazine ring, or a phenothiazine ring.

^{At least} one of the It may have a structure linked to the aryl ring or heteroaryl ring in the G ring or the I ring.

For example, the following partial structure A10 may be formed by the above connection.

In formula (A10), R ^A1 to R ^A4 are each independently hydrogen, optionally substituted alkyl, or optionally substituted cycloalkyl, and any 2 to 4 of R ^A1 to R ^A4 are connected to a linking group or single bond. They may be bonded to each other, and X is bonded to one of the two rings at the * position and to the other ring at the ** position. That is, N in equation (A10) is N of >NR ^NX when X is >NR ^NX . The cyclic atoms bonded at the two * positions may be adjacent atoms (carbon atoms are preferred). The partial structure expressed by formula (A10) includes an NC bond with a weak bond dissociation energy (BDE), but because there is another bond forming a ring, the reverse reaction (recombination reaction) is promoted even when the NC bond is cut. , resulting in a more stable structure. Therefore, an organic EL device manufactured using a polycyclic aromatic compound having this structure is expected to have a longer device life. When the polycyclic aromatic compound contains the structure represented by formula (A10), the number may be one or two.

In formula (A10), any 2 to 4 of R ^A1 to R ^A4 may be connected to each other by a linking group.

R ^A1 to R ^A4 are any two (R ^A1 and R ^A4 , R ^A1 and R ^A4 , and R ^A2 and R A3 , R A1 and R ^A2 , R ^A3 and ^{R A4 ,} R ^A1 and R ^A2 and ^R It is preferable that ^A3 and R ^A4 ) are bonded to each other by a linking group or a single bond, and it is more preferable that R ^A1 and R ^A4 are bonded to each other by a linking group or a single bond. Examples of the divalent group formed by bonding with each other include alkylene. At least one hydrogen in the alkylene may be substituted with alkyl or cycloalkyl, and at least one (preferably one) -CH ₂ - in the alkylene is -O- and -S- It may be replaced with . As the divalent group formed by bonding to each other, linear alkylene with 2 to 5 carbon atoms is preferable, linear alkylene with 3 or 4 carbon atoms is more preferable, and linear alkylene with 4 carbon atoms (-(CH ₂ ) ₄ -) is preferable. It is more desirable. It is particularly preferable that the straight-chain alkylene having 4 carbon atoms (-(CH ₂ ) ₄ -) is unsubstituted.

The remaining R ^A1 to R ^A4 that are not involved in the connection by the linking group are each independently hydrogen or optionally substituted alkyl, and more preferably optionally substituted alkyl having 1 to 6 carbon atoms, It is more preferable that it is unsubstituted alkyl with 1 to 6 carbon atoms, and most preferably it is all methyl.

That is, as the partial structure expressed by formula (A10), the structure expressed by formula (A11) below is preferable.

In formula (A11), Me is methyl, and is bonded to one of the two rings to which X is bonded at the two * positions and to the other ring at the ** positions.

<Preferred substituents>

In polycyclic aromatic compounds used as emitting dopants (in other compounds used as dopants), tertiary alkyl represented by the following formula (tR) is one of the particularly preferable substituents containing “alkyl”. This is because the distance between molecules increases due to such bulky substituents, thereby improving the luminescence quantum yield (PLQY). Additionally, a substituent in which the tertiary alkyl represented by the formula (tR) is substituted by another substituent as the second substituent is also preferable. Specifically, diarylamino substituted with tertiary alkyl represented by formula (tR), carbazolyl (preferably N-carbazolyl) substituted with tertiary alkyl represented by formula (tR), or formula and benzocarbazolyl (preferably N-benzocarbazolyl) substituted with tertiary alkyl represented by (tR). Examples of the substitution form of the group of the formula (tR) for diarylamino, carbazolyl and benzocarbazolyl include where some or all of the hydrogens of the aryl ring or benzene ring in these groups are substituted with the group of the formula (tR). You can.

In formula (tR), R ^a , R ^b , and R ^c are each independently alkyl having 1 to 24 carbon atoms, and any -CH ₂ - in the alkyl may be substituted with -O-, and the formula ( The group represented by (tR) uses * as the binding position.

The “alkyl having 1 to 24 carbon atoms” for R ^a , R ^b and R ^c may be either straight chain or branched chain, for example, straight chain alkyl having 1 to 24 carbon atoms or branched alkyl having 3 to 24 carbon atoms, Alkyl with 1 to 18 carbon atoms (branched chain alkyl with 3 to 18 carbon atoms), alkyl with 1 to 12 carbon atoms (branched chain alkyl with 3 to 12 carbon atoms), alkyl with 1 to 6 carbon atoms (branched chain alkyl with 3 to 6 carbon atoms) , alkyl with 1 to 4 carbon atoms (branched chain alkyl with 3 to 4 carbon atoms).

The total number of carbon atoms of R ^a , R ^b , and R ^c in the formula (tR) is preferably 3 to 20 carbon atoms, and particularly preferably 3 to 10 carbon atoms.

Specific alkyls for R ^a , R ^b , and R ^c include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, s-butyl, t-butyl, n-pentyl, isopentyl, neopentyl, t-pentyl, n-hexyl, 1-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, n-heptyl, 1-methylhexyl, n-octyl, t-octyl, 1-methylheptyl, 2-ethylhexyl, 2-propylpentyl, n-nonyl, 2,2-dimethylheptyl, 2,6-dimethyl-4-heptyl, 3,5,5-trimethylhexyl, n-decyl, n -Undecyl, 1-methyldecyl, n-dodecyl, n-tridecyl, 1-hexylheptyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n -Eicosil, etc. can be mentioned.

Examples of the group represented by the formula (tR) include t-butyl, t-amyl, 1-ethyl-1-methylpropyl, 1,1-diethylpropyl, 1,1-dimethylbutyl, and 1-ethyl-1. -Methylbutyl, 1,1,3,3-tetramethylbutyl, 1,1,4-trimethylpentyl, 1,1,2-trimethylpropyl, 1,1-dimethyl octyl, 1,1-dimethylpentyl, 1, 1-dimethylheptyl, 1,1,5-trimethylhexyl, 1-ethyl-1-methylhexyl, 1-ethyl-1,3-dimethylbutyl, 1,1,2,2-tetramethylpropyl, 1-butyl- 1-Methylpentyl, 1,1-diethylbutyl, 1-ethyl-1-methylpentyl, 1,1,3-trimethylbutyl, 1-propyl-1-methylpentyl, 1,1,2-trimethylpropyl, 1 -Ethyl-1,2,2-trimethylpropyl, 1-propyl-1-methylbutyl, 1,1-dimethylhexyl, etc. Among these, t-butyl and t-amyl are preferred.

As the substituent, the substituent represented by formula (A30) is also preferable.

In equation (A30),

Ak is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted cycloalkyl, or substituted or unsubstituted cycloalkenyl, and at least One -CH ₂ - may be substituted with -O- or -S-,

R ^Ak is substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^Ak may be bonded to Ak through a linking group or single bond. , * is the binding position.

In formula (A30), since Ak is the above-mentioned substituent and does not conjugate with the lone pair of electrons on N, the lone pair can be conjugated with the π electron of the binding site, and the wavelength is larger than when there is an aryl etc. at the same position. Change is possible. In addition, the same applies to the influence on the multiple resonance effect, so that greater improvement in thermally activated delayed fluorescence (TADF) properties is possible.

R ^Ak is preferably aryl which may be substituted by alkyl or cycloalkyl, heteroaryl which may be substituted by alkyl or cycloalkyl, alkyl or cycloalkyl, aryl which may be substituted by alkyl, or heteroaryl which may be substituted by alkyl. Aryl, alkyl or cycloalkyl is more preferable, aryl which may be substituted with alkyl is still more preferable, and phenyl which may be substituted with methyl is particularly preferable.

In formula (A30), Ak is preferably alkyl with 1 to 6 carbon atoms or cycloalkyl with 3 to 14 carbon atoms, preferably alkyl with 1 to 4 carbon atoms or cycloalkyl with 3 to 8 carbon atoms, and preferably has 1 to 4 carbon atoms. It is more preferable that it is alkyl, and even more preferably it is methyl.

R ^Ak and Ak may be the same or different, and are preferably different.

R ^Ak may be bonded to Ak through a linking group or single bond. The linking group at this time includes >O, >S, or >Si(-R) ₂ . >R in Si(-R) ₂ is hydrogen, aryl with 6 to 12 carbon atoms, alkyl with 1 to 6 carbon atoms, or cycloalkyl with 3 to 14 carbon atoms. Examples of structures in which R ^Ak is bonded to Ak through a linking group or single bond include the following.

In each of the above formulas, * represents a binding position.

The emission wavelength can be adjusted by the structural steric hindrance, electron donating, and electron withdrawing properties of the substituent of the compound used as a dopant (assisting dopant or emitting dopant). Preferably, it is a group represented by the following structural formula, more preferably methyl, t-butyl, t-amyl, t-octyl, neopentyl, adamantyl, phenyl, o-tolyl, p-tolyl, 2, 4-xylyl, 2,5-xylyl, 2,6-xylyl, 2,4,6-mesityl, diphenylamino, di-p-tolylamino, bis(p-(t-butyl)phenyl) Amino, carbazolyl, 3,6-dimethylcarbazolyl, 3,6-di-t-butylcarbazolyl and phenoxy, more preferably methyl, t-butyl, t-amyl, t- Octyl, neopentyl, adamantyl, phenyl, o-tolyl, 2,6-xylyl, 2,4,6-mesityl, diphenylamino, di-p-tolylamino, bis(p-(t-butyl) )phenyl)amino, carbazolyl, 3,6-dimethylcarbazolyl and 3,6-di-t-butylcarbazolyl and tribenzoazepinyl. From the viewpoint of ease of synthesis, greater steric hindrance is preferable for selective synthesis, specifically, t-butyl, t-amyl, t-octyl, adamantyl, o-tolyl, p-tolyl, 2, 4-xylyl, 2,5-xylyl, 2,6-xylyl, 2,4,6-mesityl, di-p-tolylamino, bis(p-(t-butyl)phenyl)amino, 3, 6-dimethylcarbazolyl and 3,6-di-t-butylcarbazolyl are preferred.

In the structural formula below, * represents the binding position.

Polycyclic aromatic compounds having a structure containing a structural unit represented by formula (1) or formula (2) include tertiary alkyl (t-butyl or t-amyl, etc.), neopentyl, etc., represented by the above-mentioned formula (tR). Alternatively, it is preferable that the structure contains at least one adamantyl, and it is preferable that it contains a tertiary alkyl (t-butyl or t-amyl, etc.) represented by the formula (tR). This is because the distance between molecules increases due to such bulky substituents, thereby improving the luminescence quantum yield (PLQY). Moreover, as a substituent, diarylamino is also preferable. Furthermore, diarylamino substituted with a group of the formula (tR), carbazolyl (preferably N-carbazolyl) substituted with a group of the formula (tR), or benzocarbazolyl (preferably N-carbazolyl) substituted with a group of the formula (tR) Preferably, N-benzocarbazolyl) is also preferred. Examples of the substitution form of the group of formula (tR) for diarylamino, carbazolyl and benzocarbazolyl include where some or all of the hydrogens of the aryl ring or benzene ring in this group are substituted with a group of formula (tR). You can.

In the structure containing the structural unit represented by Formula (1) or Formula (2), the substituent of the aryl ring or heteroaryl ring may be a substituent represented by the following formula (A20).

The substituent represented by the formula (A20) is bonded to two atoms adjacent to each of the two * atoms in the ring of the aryl ring or heteroaryl ring. In formula (A20), L is >NR, >O, >Si(-R) ₂ or >S, and R of >NR is substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or It is unsubstituted alkyl or substituted or unsubstituted cycloalkyl, and R in >Si(-R) ₂ is hydrogen, optionally substituted aryl, optionally substituted alkyl, or optionally substituted cycloalkyl, and is also a linking group. may be bonded to each other, and at least one of the >NR and the R of >Si(-R) ₂ may be bonded to the aryl ring or heteroaryl ring through a linking group or single bond,

r is an integer from 1 to 4,

R ^A is each independently hydrogen, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and any R ^A may be bonded to any other R ^A through a linking group or single bond.

Examples of the above substituents include substituents represented by any of the following.

In each formula, in *, it may be bonded to two or three consecutive (adjacent) atoms in the ring of any one aryl ring or heteroaryl ring, respectively.

<Cycloalkane condensation>

At least one selected from the group consisting of an aryl ring and a heteroaryl ring in a polyaromatic compound having a structure containing a structural unit represented by formula (1) or formula (2) is condensed with at least one cycloalkane. It can be done. The same applies to polycyclic aromatic compounds represented by any formula selected from the group consisting of formulas (1-a) to formula (1-l) and formulas (2-a) to formula (2-l), as described below. The same applies to polycyclic aromatic compounds expressed by any of these formulas.

The cycloalkane may be any cycloalkane having 3 to 24 carbon atoms. At this time, at least one hydrogen in the cycloalkane may be substituted with aryl with 6 to 30 carbon atoms, heteroaryl with 2 to 30 carbon atoms, alkyl with 1 to 24 carbon atoms, or cycloalkyl with 3 to 24 carbon atoms, and the corresponding At least one -CH ₂ - in the cycloalkane may be substituted with -O-.

Cycloalkane is a cycloalkane having 3 to 20 carbon atoms, and at least one hydrogen in the cycloalkane is aryl with 6 to 16 carbon atoms, heteroaryl with 2 to 22 carbon atoms, alkyl with 1 to 12 carbon atoms, or 3 to 3 carbon atoms. It is preferable that it is a cycloalkane which may be substituted with cycloalkyl of 16.

As “cycloalkane”, cycloalkane with 3 to 24 carbon atoms, cycloalkane with 3 to 20 carbon atoms, cycloalkane with 3 to 16 carbon atoms, cycloalkane with 3 to 14 carbon atoms, cycloalkane with 5 to 10 carbon atoms, cycloalkane with 5 to 8 carbon atoms. cycloalkanes, cycloalkanes with 5 to 6 carbon atoms, cycloalkanes with 5 carbon atoms, etc.

Specific cycloalkanes include cyclopropane, cyclobutane, cyclopentane, cyclohexane, cycloheptane, cyclooctane, cyclononane, cyclodecane, norbonane (bicyclo[2.2.1]heptane), and bicyclo[1.1.0]butane. , bicyclo[1.1.1]pentane, bicyclo[2.1.0]pentane, bicyclo[2.1.1]hexane, bicyclo[3.1.0]hexane, bicyclo[2.2.2]octane, adamantane, Diamantane, decahydronaphthalene, and decahydroazulene, and alkyl (especially methyl) substituted products thereof having 1 to 5 carbon atoms, halogen (particularly fluorine) substituted products, and deuterium substituted products.

Among the above examples, at least one carbon at the α position of the cycloalkane (the carbon adjacent to the carbon at the condensation site in cycloalkanes condensing to an aryl ring or heteroaryl ring), for example, as shown in the structural formula below: A structure with a substituent is preferable, a structure with two substituents on the carbon at the α position is more preferable, and a structure with both carbons at the α position having two substituents (a total of four substituents) is more preferable. desirable. Examples of this substituent include alkyl having 1 to 5 carbon atoms (especially methyl), halogen (especially fluorine), and deuterium. In particular, it is preferable to have a structure in which a partial structure represented by the following formula (B) is bonded to an adjacent carbon atom in the aryl ring or heteroaryl ring.

In formula (B), * represents the binding position.

The number of cycloalkanes condensed to one aryl ring or heteroaryl ring is preferably 1 to 3, more preferably 1 or 2, and even more preferably 1. For example, examples of condensation of one or more cycloalkanes on one benzene ring (phenyl) are shown below. * indicates a bonding position, and the position may be any of the carbons that form a benzene ring but do not form a cycloalkane. Condensed cycloalkanes may be condensed as shown in formula (Cy-1-4) and formula (Cy-2-4). This applies even if the ring (group) to be condensed is an aryl ring or heteroaryl ring other than a benzene ring (phenyl), and even if the cycloalkane to be condensed is a cycloalkane other than cyclopentane or cyclohexane.

At least one -CH ₂ - in the cycloalkane may be substituted with -O-. For example, an example in which one or more -CH ₂ - in a cycloalkane condensed to one benzene ring (phenyl) is replaced with -O- is shown below. This applies even if the ring (group) to be condensed is an aryl ring or heteroaryl ring other than a benzene ring (phenyl), and even if the cycloalkane to be condensed is a cycloalkane other than cyclopentane or cyclohexane.

The cycloalkane may be substituted with at least one substituent, and the substituent may be any one selected from the substituent group Z. Among these substituents, alkyl (for example, alkyl with 1 to 6 carbon atoms) and cycloalkyl (for example, cycloalkyl with 3 to 14 carbon atoms) are preferable. Additionally, it is also preferable that one of the hydrogens is replaced with halogen (for example, fluorine) or deuterium. Additionally, when cycloalkyl is substituted, it may be in a form of substitution that forms a spiro structure. For example, an example of a spiro structure formed in a cycloalkane condensed to one benzene ring (phenyl) is shown below. * in each structural formula means, in the case of a benzene ring, a benzene ring included in the skeletal structure of the compound, and in the case of phenyl, it means a bond substituted in the skeletal structure of the compound.

As a form of cycloalkane condensation, first, in a polycyclic aromatic compound having a structure containing a structural unit represented by formula (1) or formula (2), ring B, ring C, ring D, ring E, ring F, Examples include forms in which the aryl ring and heteroaryl ring in each of the G ring, H ring, and I ring are condensed with cycloalkane.

As another form of cycloalkane condensation, a polyaromatic compound having a structure containing a structural unit represented by formula (1) or formula (2), for example, >NR ^NX where R ^NX is an aryl condensed with cycloalkane. , diarylamino condensed with a cycloalkane (condensed at this aryl portion), carbazolyl condensed with a cycloalkane (condensed at this benzene ring portion), or benzocarbazolyl condensed with a cycloalkane (condensed at this benzene ring portion). ) can be given as an example.

Additionally, by introducing a cycloalkane structure into a polycyclic aromatic compound having a structure containing a structural unit represented by formula (1) or formula (2), a further decrease in melting point or sublimation temperature can be expected. This means that in sublimation purification, which is almost essential as a purification method for materials for organic devices such as organic EL elements that require high purity, thermal decomposition of the material can be avoided because purification can be done at a relatively low temperature. Additionally, this also applies to the vacuum deposition process, which is a powerful means for manufacturing organic devices such as organic EL elements. Since the process can be performed at a relatively low temperature, thermal decomposition of the material can be avoided, resulting in high-performance organic devices. You can get it. Additionally, since solubility in organic solvents is improved by introducing a cycloalkane structure, it becomes possible to apply it to device manufacturing using a coating process. However, the present invention is not particularly limited to this principle.

<Substitution by deuterium, cyano, or halogen>

All or part of the hydrogen in the structure containing the structural unit expressed by formula (1) or formula (2) may be deuterium, cyano, or halogen. The same applies to a structure expressed by any formula selected from the group consisting of formulas (1-a) to formula (1-l) and formulas (2-a) to formula (2-l), and the following explanation is The same applies to polycyclic aromatic compounds expressed by any one formula selected from the group consisting of Formulas (1-a) to Formulas (1-l) and Formulas (2-a) to Formulas (2-l).

For example, in the structure containing the structural unit represented by formula (1) or formula (2), ring B, ring C, ring D, ring E, ring F, ring G, ring H, and ring Aryl ring or heteroaryl ring, B ring, C ring, D ring, E ring, F ring, G ring, H ring, and substituents of aryl ring or heteroaryl ring in I ring, and Hydrogen in R ^NX , R ^CX , or R ^IX (=alkyl, cycloalkyl, aryl, or heteroaryl) when NR ^NX , >C(-R ^CX ) ₂ , or >Si(-R ^IX ) ₂ may be substituted with deuterium, cyano, or halogen, but among these, an embodiment in which all or part of the hydrogen in aryl or heteroaryl is substituted with deuterium, cyano, or halogen can be mentioned. Halogen is fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine, or bromine, more preferably fluorine or chlorine, and fluorine is more preferable. Also, from the viewpoint of durability, it is preferable that all or part of the hydrogen in the structure containing the structural unit expressed by formula (1) or formula (2) is deuterated.

<Specific examples of polycyclic aromatic compounds of the present invention>

Specific examples of the polycyclic aromatic compound of the present invention include compounds represented by any of the following structural formulas.

<Explanation of high molecular weight of polycyclic aromatic compounds>

A polycyclic aromatic compound having a structure containing a structural unit represented by Formula (1) or Formula (2) is a polymer compound obtained by polymerizing a reactive compound substituted with a reactive substituent as a monomer (see above for obtaining this polymer compound). monomer has a polymerizable substituent), or a polymer crosslinked product obtained by further crosslinking the polymer compound (the polymer compound to obtain this polymer crosslinked product has a crosslinkable substituent), or a main chain polymer and the reactive compound A reacted pendant-type polymer compound (the reactive compound to obtain this pendant-type polymer compound has a reactive substituent), or a pendant-type polymer cross-linked product further crosslinked with the pendant-type polymer compound (to obtain this pendant-type polymer cross-linked product) The pendant polymer compound has a crosslinkable substituent) and can also be used as a material for organic devices, such as a material for an organic electroluminescent device, a material for an organic field effect transistor, a material for an organic thin film solar cell, or a wavelength conversion filter. there is.

Meanwhile, in the present specification, “polymer compound” means a polymer that has a molecular weight distribution and a number average molecular weight of 1X10 ³ to 1X10 ⁸ (1X10^3 to 1X10^8) in terms of polystyrene. The number average molecular weight (Mn) of a polymer compound in terms of polystyrene can be determined by size exclusion chromatography (SEC) using tetrahydrofuran as the mobile phase. Specifically, the polymer compound to be measured is dissolved in tetrahydrofuran at a concentration of about 0.05% by mass, and 10 μL is injected into the SEC. The flow rate of the mobile phase is 1.0 mL/min, and PLgelMIXED_B (manufactured by Polymer Laboratories) is used as a column. A UV_VIS detector (Tosoh, brand name: UV-8320GPC) can be used as the detector.

The polymer compound of the present invention preferably has a number average molecular weight of 2000 to 1X10 ⁸ , and more preferably 5000 to 1X10 ⁸ .

The above-mentioned reactive substituent (including the polymerizable substituent, the crosslinkable substituent, and the reactive substituent for obtaining a pendant polymer, hereinafter also simply referred to as “reactive substituent”) can increase the molecular weight of the polycyclic aromatic compound. There is no particular limitation as long as it is a substituent that is present, a substituent that can further crosslink the polymer compound thus obtained, and a substituent that can pendantly react with the main chain polymer, but a substituent with the following structure is preferable. * in each structural formula indicates the binding position.

L is each independently a single bond, -O-, -S-, >C=O, -O-C(=O)-, alkylene with 1 to 12 carbon atoms, oxyalkylene with 1 to 12 carbon atoms, and 1 carbon atom It is a polyoxyalkylene of ~12. Among the above substituents, groups represented by formula (XLS-1), formula (XLS-2), formula (XLS-3), formula (XLS-9), formula (XLS-10), or formula (XLS-17) are preferable. And, the group represented by formula (XLS-1), formula (XLS-3), or formula (XLS-17) is more preferable.

These polymer compounds, polymer cross-linked products, pendant-type polymer compounds, and pendant-type polymer cross-linked products include in addition to the repeating units of the polycyclic aromatic compound consisting of one or two or more structural units represented by formula (1) or formula (2). , substituted or unsubstituted triarylamine, substituted or unsubstituted fluorene, substituted or unsubstituted anthracene, substituted or unsubstituted tetracene, substituted or unsubstituted triazine, substituted or unsubstituted carbazole, substituted or from the group consisting of unsubstituted tetraphenylsilane, substituted or unsubstituted spirofluorene, substituted or unsubstituted triphenylphosphine, substituted or unsubstituted dibenzothiophene, and substituted or unsubstituted dibenzofuran. At least one selected type may be included as a repeating unit.

Substituents in these repeating units include, for example, aryl, heteroaryl, diarylamino, diheteroarylamino, arylheteroarylamino, and diarylboryl (two aryls may be bonded through a single bond or a linking group. ), alkyl, cycloalkyl, alkoxy, aryloxy, trialrylsilyl, trialkylsilyl, tricycloalkylsilyl, dialkylcycloalkylsilyl, or alkyldicycloalkylsilyl. For details about “aryl” of triarylamine and these substituents, the explanations in Formulas (1) and (2) can be cited.

<Method for producing polycyclic aromatic compounds>

A polycyclic aromatic compound having a structure containing a structural unit represented by formula (1) or formula (2) is basically formed by first bonding the a ring and the B to I ring (b to i ring) with a linking group. Intermediate 1 is prepared (first reaction), B ring (b ring), G ring (g ring), I ring (i ring), E ring (e ring), F ring (f ring), and H ring. (h ring) is bonded with boron to form a condensed ring to obtain intermediate 2 (second reaction), and then the condensed ring including the a ring and B to I rings (b to i rings) is bonded to boron. The final product can be manufactured by doing this (third reaction).

In the first reaction, general reactions such as Birchwald-Hartwig reaction, nucleophilic substitution reaction, and Goldberg reaction can be used. Additionally, in the second and third reactions, a tandem hetero Friedel Crafts reaction (successive aromatic electron substitution reaction, the same applies hereinafter) can be used. An example is shown in scheme (0).

The second reaction is, as shown in scheme (1) or (2) below, the B ring (b ring), the G ring (g ring), and the I ring (i ring), and the E ring (e ring) and F ring. This is a reaction that introduces boron that bonds the (f ring) and H ring (h ring). The halogen in the intermediate is halogen-metal exchanged with n-butyllithium, sec-butyllithium, or t-butyllithium, and then a boronating agent is added to perform lithium-boron metal exchange, followed by addition of a Brønsted base. By conducting a tandem Bora Friedel Crafts reaction, Intermediate 2, which becomes a precursor for the third reaction, can be obtained.

The third reaction is a reaction to introduce boron that binds the condensed ring including the a ring and the B to I rings (b to i rings), as shown in scheme (1) or (2) below. By adding a boronating agent such as boron tribromide or boron triiodide and a Bronsted base such as N,N-diisopropylethylamine or 2,6-di-tertiarybutylpyridine to the intermediate, tandem Bora Friedel Crafts By reacting, the target product can be obtained. In the third reaction, a Lewis acid such as aluminum trichloride may be added to promote the reaction.

Meanwhile, the halogen atom (Hal) in the above scheme (0) and the schemes below may be any of F, Cl, Br, and I, and can be appropriately selected in consideration of the reactivity of the substrate.

In the B ring, C ring, D ring, E ring, F ring, G ring, H ring, and I ring in the formula representing the intermediate, etc., the bond is not indicated as indicated by the arrow in the formula (IntC1) below. It is assumed that hydrogen is bonded to the site as shown in the formula (IntC2) below.

The above scheme (1) or (2) mainly shows a method for producing a polycyclic aromatic compound having a structure containing one structural unit represented by formula (1) or formula (2), but two structural units are used. The polycyclic aromatic compounds included above can be produced by using an intermediate having a plurality of a rings and B to I rings (b to i rings).

By appropriately selecting the raw materials to be used, a polycyclic aromatic compound having a substituent at a desired position can be synthesized.

Specific examples of solvents used in the above reaction include toluene, t-butyl benzene, and xylene.

On the other hand, as the orthometalation reagent used in the schemes (1) and (2), alkyl lithium such as methyl lithium, n-butyllithium, sec-butyllithium, and t-butyllithium, lithium diisopropylamide, and lithium tetra. Organic alkali metal compounds such as methyl piperidide, lithium hexamethyl disilazide, and potassium hexamethyl disilazide can be mentioned.

On the other hand, as the metal-boron metal exchange reagent used in the above schemes (1) and (2), boron halides such as boron trifluoride, boron trichloride, boron tribromide, and boron triiodide, boron alkoxides, and boron Aryloxy compounds, etc. are mentioned.

Meanwhile, the Bronsted base used in the above schemes (1) and (2) include 2,6-di-tertiarybutylpyridine, N,N-diisopropylethylamine, triethylamine, 2,2,6 ,6-Tetramethylpiperidine, 1,2,2,6,6-pentamethylpiperidine, N,N-dimethylaniline, N,N-dimethyltoluidine, 2,6-lutidine, sodium tetraphenyl borate , potassium tetraphenylborate, triphenylborane, tetraphenylsilane, Ar ₄ BNa, Ar ₄ BK, Ar ₃ B, Ar ₄ Si (where Ar is an aryl such as phenyl).

Lewis acids used in the schemes (1) and (2) include AlCl ₃ , AlBr ₃ , AlF ₃ , BF ₃ ·OEt ₂ , BCl ₃ , BBr ₃ , BI ₃ , GaCl ₃ , GaBr ₃ , InCl ₃ , InBr ₃ , In(OTf) ₃ , SnCl ₄ , SnBr ₄ , AgOTf, ScCl ₃ , Sc(OTf) ₃ , ZnCl ₂ , ZnBr ₂ , Zn(OTf) ₂ , MgCl ₂ , MgBr ₂ , Mg(OTf) ₂ , LiOTf , NaOTf, KOTf, Me ₃ SiOTf, Cu(OTf) ₂ , CuCl ₂ , YCl ₃ , Y(OTf) ₃ , TiCl ₄ , TiBr ₄ , ZrCl ₄ , ZrBr ₄ , FeCl ₃ , FeBr ₃ , CoCl ₃ , CoBr ₃ etc. can be mentioned.

In the above schemes (1) and (2), a Bronsted base or Lewis acid may be used to promote the tandem hetero Friedel-Crafts reaction. However, when using boron halides such as boron trifluoride, boron trichloride, boron tribromide, and boron triiodide, acids such as hydrogen fluoride, hydrogen chloride, hydrogen bromide, and hydrogen iodide are formed as the aromatic electron substitution reaction progresses. Because it is produced, the use of a Brønsted base to capture the acid is effective. On the other hand, when an aminated halide of boron or an alkoxylate of boron is used, amines and alcohols are produced as the aromatic electron substitution reaction progresses, so in most cases, there is no need to use a Brønsted base. Since the detachment ability of amino or alkoxy is low, the use of a Lewis acid that promotes detachment is effective.

In addition, the polycyclic aromatic compounds of the present invention include those in which at least some of the hydrogen atoms are substituted with deuterium or those in which at least some of the hydrogen atoms are substituted with halogens such as fluorine or chlorine. These compounds are made from raw materials in which the desired position is deuterated, fluorinated, or chlorinated. It can be synthesized in the same manner as above by using .

2. Organic device

The polycyclic aromatic compound of the present invention can be used as a material for organic devices. Examples of organic devices include organic electroluminescent elements, organic field-effect transistors, and organic thin-film solar cells.

The polycyclic aromatic compound according to the present invention can be used as a material for organic devices. Examples of organic devices include organic electroluminescent devices, organic field-effect transistors, and organic thin-film solar cells, but it is preferable that they are organic electroluminescent devices. The polycyclic aromatic compound according to the present invention is preferably an organic electroluminescent device material, more preferably a material for a light-emitting layer (light-emitting material), and most preferably a dopant material for the light-emitting layer.

2-1. abandonment electric field light emitting element

An organic electroluminescent element has a pair of electrodes consisting of an anode and a cathode, and a light-emitting layer disposed between the pair of electrodes. The organic electroluminescent element may further have other organic layers.

2-1-1. abandonment electric field Structure of light emitting device

1 is a schematic cross-sectional view showing an example of an organic EL device.

The organic EL device 100 shown in FIG. 1 includes a substrate 101, an anode 102 provided on the substrate 101, a hole injection layer 103 provided on the anode 102, and a hole injection layer. A hole transport layer 104 provided on (103), a light-emitting layer 105 provided on the hole transport layer 104, an electron transport layer 106 provided on the light-emitting layer 105, and an electron provided on the electron transport layer 106. It has an injection layer 107 and a cathode 108 provided on the electron injection layer 107.

In addition, the organic EL element 100 reverses the manufacturing order, for example, a substrate 101, a cathode 108 provided on the substrate 101, and an electron injection layer provided on the cathode 108 ( 107), an electron transport layer 106 provided on the electron injection layer 107, a light emitting layer 105 provided on the electron transport layer 106, a hole transport layer 104 provided on the light emitting layer 105, and a hole transport layer. It may be configured to include a hole injection layer 103 provided on (104) and an anode 102 provided on the hole injection layer 103.

It is not necessary to have all of the above layers, and the minimum structural unit is composed of an anode 102, a light emitting layer 105, and a cathode 108, and a hole injection layer 103, a hole transport layer 104, and an electron transport layer 106. ), the electron injection layer 107 is a layer installed arbitrarily. In addition, each of the above layers may be composed of a single layer or may be composed of multiple layers.

As aspects of the layers constituting the organic EL element, in addition to the above-mentioned “substrate/anode/hole injection layer/hole transport layer/light-emitting layer/electron transport layer/electron injection layer/cathode”, “substrate/anode/hole transport layer/cathode” Light-emitting layer/electron transport layer/electron injection layer/cathode”, “substrate/anode/hole injection layer/light-emitting layer/electron transport layer/electron injection layer/cathode”, “substrate/anode/hole injection layer/hole transport layer/light-emitting layer/electron injection layer” /cathode”, “substrate/anode/hole injection layer/hole transport layer/light emitting layer/electron transport layer/cathode”, “substrate/anode/light emitting layer/electron transport layer/electron injection layer/cathode”, “substrate/anode/hole transport layer/light emitting layer” /electron injection layer/cathode”, “substrate/anode/hole transport layer/light-emitting layer/electron transport layer/cathode”, “substrate/anode/hole injection layer/light-emitting layer/electron injection layer/cathode”, “substrate/anode/hole injection layer” /light-emitting layer/electron transport layer/cathode”, “substrate/anode/light-emitting layer/electron transport layer/cathode”, or “substrate/anode/light-emitting layer/electron injection layer/cathode” may be used.

The organic EL element may have one or both of an electron blocking layer (electron blocking layer) and a hole blocking layer (hole blocking layer). The electron blocking layer has a LUMO shallower than that of the light-emitting layer and a HOMO closer to the light-emitting layer or the hole transport layer, and is disposed between the light-emitting layer and the hole transport layer. Since electrons remain in the light-emitting layer and do not leak out to the hole transport layer, shortening of the lifespan due to deterioration of the hole transport layer and reduction in efficiency due to a decrease in recombination efficiency can be prevented. The hole blocking layer has a HOMO that is deeper than the light-emitting layer and a LUMO that is closer to the light-emitting layer or the hole transport layer, and is disposed between the light-emitting layer and the electron transport layer. Since the holes remain in the light-emitting layer and do not leak out to the electron transport layer, shortening of the lifespan due to deterioration of the electron transport layer and reduction in efficiency due to a decrease in recombination efficiency can be prevented. The hole injection/transport layer may also serve as an electron blocking layer. The electron injection/transport layer may also serve as a hole blocking layer.

The organic EL element may further have a high T1 layer. The high T1 layer has a T1 higher than that of the host compound, assisting dopant compound, or emitting dopant compound used in the light emitting layer, and is disposed between the light emitting layer and the hole transport layer and/or between the light emitting layer and the electron blocking layer. The value of T1 energy varies depending on the light emitting mechanism of the device, but has a higher T1 than the compound used as the host. By having a high T1 layer around the light-emitting layer, triplet energy is confined and triplet energy, which does not normally lead to light emission in fluorescent molecules, is converted into singlet energy, thereby achieving high efficiency. The hole injection/transport layer or the electron blocking layer may also serve as the high T1 layer. The electron injection/transport layer or the hole blocking layer may also serve as the high T1 layer.

2-1-2. abandonment electric field radiation in the device Board

The substrate 101 is a support for the organic EL element 100, and usually quartz, glass, metal, plastic, etc. are used. The substrate 101 is formed in a plate shape, a film shape, or a sheet shape depending on the purpose, and for example, a glass plate, a metal plate, a metal foil, a plastic film, a plastic sheet, etc. are used. Among them, glass plates and plates made of transparent synthetic resins such as polyester, polymethacrylate, polycarbonate, and polysulfone are preferable. In the case of a glass substrate, soda lime glass, alkali-free glass, etc. are used, and the thickness may be sufficient to maintain mechanical strength. In addition, in order to increase the gas barrier property, the substrate 101 may be formed with a gas barrier film such as a dense silicon oxide film on at least one side. In particular, a plate, film or sheet made of synthetic resin with low gas barrier property may be used as the substrate. When using (101), it is desirable to form a gas barrier film.

2-1-3. abandonment electric field radiation in the device anode

The anode 102 serves to inject holes into the light emitting layer 105. On the other hand, when at least one of the hole injection layer 103 and the hole transport layer 104 is provided between the anode 102 and the light emitting layer 105, holes are injected into the light emitting layer 105 through these layers. do.

Materials forming the anode 102 include inorganic compounds and organic compounds. Inorganic compounds include, for example, metals (aluminum, gold, silver, nickel, palladium, chromium, etc.), metal oxides (indium oxide, tin oxide, indium-tin oxide (ITO), indium-zinc oxide (IZO) etc.), halogenated metals (copper iodide, etc.), copper sulfide, carbon black, ITO glass, Nesa glass, etc. Examples of organic compounds include polythiophenes such as poly(3-methylthiophene), and conductive polymers such as polypyrrole and polyaniline. In addition, it can be used by appropriately selecting from among materials used as anodes for organic EL devices.

2-1-4. abandonment electric field radiation in the device hole injection layer , hole transport layer

The hole injection layer 103 serves to efficiently inject holes moving from the anode 102 into the light emitting layer 105 or the hole transport layer 104. The hole transport layer 104 serves to efficiently transport holes injected from the anode 102 or holes injected from the anode 102 through the hole injection layer 103 to the light emitting layer 105. The hole injection layer 103 and the hole transport layer 104 are formed by laminating or mixing one or two or more types of hole injection/transport materials, respectively. Additionally, an inorganic salt such as iron (III) chloride may be added to the hole injection/transport material to form a layer.

As a hole injection/transport material, it is necessary to efficiently inject and transport holes from the positive electrode between electrodes to which an electric field is applied, and it is desirable to have high hole injection efficiency and efficiently transport the injected holes. To achieve this, it is desirable to use a material that has a small ionization potential, has a large hole mobility, has excellent stability, and is unlikely to generate trapping impurities during production and use.

Materials forming the hole injection layer 103 and the hole transport layer 104 include compounds conventionally used as hole charge transport materials in photoconductive materials, p-type semiconductors, and hole injection layers and holes in organic EL devices. Any compound can be selected and used among known compounds used in the transport layer. Specific examples of these include carbazole derivatives (N-phenylcarbazole, polyvinylcarbazole, etc.), biscarbazole derivatives such as bis(N-arylcarbazole) or bis(N-alkylcarbazole), and triarylamine. Derivatives (polymers with aromatic tertiary amino in the main or side chain, 1,1-bis(4-di-p-tolylaminophenyl)cyclohexane, N,N'-diphenyl-N,N'-di (3-methylphenyl)-4,4'-diaminobiphenyl, N,N'-diphenyl-N,N'-dinaphthyl-4,4'-diaminobiphenyl, N,N'-diphenyl -N,N'-di(3-methylphenyl)-4,4'-diphenyl-1,1'-diamine, N,N'-dinaphthyl-N,N'-diphenyl-4,4'- Diphenyl-1,1'-diamine, N ⁴ ,N ^{4 '} -diphenyl-N ⁴ ,N ^{4 '} -bis(9-phenyl-9H-carbazol-3-yl)-[1,1'-bi Phenyl]-4,4'-diamine, N ⁴ ,N ⁴ ,N ^{4 '} ,N ^4' -tetra[1,1'-biphenyl]-4-yl)-[1,1'-biphenyl]- Triphenylamine derivatives such as 4,4'-diamine, 4,4',4"-tris(3-methylphenyl(phenyl)amino)triphenylamine, starburstamine derivatives, etc.), stilbene derivatives, phthalocyanine derivatives (free) metal, copper phthalocyanine, etc.), pyrazoline derivatives, hydrazone compounds, benzofuran derivatives or thiophene derivatives, oxadiazole derivatives, quinoxaline derivatives (e.g. 1,4,5,8,9,12-hexaaza triphenylene-2,3,6,7,10,11-hexacarbonitrile, etc.), heterocyclic compounds such as porphyrin derivatives, polysilanes, etc. In the polymer system, polycarbonate or styrene derivatives having the above-mentioned monomer in the side chain. , polyvinylcarbazole, polysilane, etc. are preferable, but there is no particular limitation as long as it is a compound that can form a thin film necessary for manufacturing a light-emitting device, can inject holes from the anode, and can further transport holes.

Additionally, it is known that the conductivity of an organic semiconductor is strongly influenced by its doping. Such an organic semiconductor matrix material is composed of a compound with good electron donating properties or a compound with good electron accepting properties. For doping of electron-donating materials, strong electron acceptors such as tetracyanoquinonedimethane (TCNQ) or 2,3,5,6-tetrafluorotetracyano-1,4-benzoquinonedimethane (F4TCNQ) are used. It is known (e.g., “M.Pfeiffer, A.Beyer, T.Fritz, K.Leo, Appl. Phys. Lett., 73(22), 3202-3204 (1998)” and “J.Blochwitz , M. Pfeiffer, T. Fritz, K. Leo, Appl. Phys. Lett., 73(6), 729-731 (1998)”). These generate so-called holes through an electron transfer process in an electron-donating base material (hole transport material). Depending on the number and mobility of holes, the conductivity of the base material changes significantly. As matrix materials having hole transport properties, for example, benzidine derivatives (TPD, etc.) or starburst amine derivatives (TDATA, etc.), or specific metal phthalocyanines (especially zinc phthalocyanine (ZnPc), etc.) are known (Japanese Patent Publication) Publication No. 2005-167175).

The above-described hole injection layer material and hole transport layer material are polymer compounds obtained by polymerizing a reactive compound substituted with a reactive substituent as a monomer, or a polymer crosslinked product thereof, or a main chain polymer reacted with the reactive compound. The pendant-type polymer compound or its pendant-type polymer crosslinked product can also be used in the material for the hole layer.

2-1-5. abandonment electric field radiation in elements luminescent layer

The light-emitting layer 105 is a layer that emits light by recombining holes injected from the anode 102 and electrons injected from the cathode 108 between electrodes to which an electric field is applied. The material forming the light-emitting layer 105 can be any compound (luminescent compound) that is excited and emits light by recombination of holes and electrons, and can form a stable thin film shape, and has strong luminescence (fluorescence) efficiency in the solid state. Compounds representing are preferably used.

The light-emitting layer preferably contains at least two materials selected from the group consisting of an emitting dopant, a hole-transporting host material, an electron-transporting host material, and an assisting dopant material. The light-emitting layer may be a single layer or a plurality of layers, and each is formed from a material for the light-emitting layer. When the light-emitting layer is composed of multiple layers, it is preferable that any one layer contains the polycyclic aromatic compound of the present invention. The light emitting layer is preferably a single layer. The emitting dopant may be contained entirely or partially in the host material. As a doping method, it can be formed by co-deposition with the host material, but may be deposited simultaneously after mixing with the host material in advance.

The amount of host material used varies depending on the type of host material, and can be determined according to the characteristics of the host material. The standard for the amount of host material used is preferably 50 to 99.999 mass% of the total mass of the light emitting layer material, more preferably 80 to 99.95 mass%, and even more preferably 90 to 99.9 mass%. When the host material is a combination of a hole-transporting host material and an electron-transporting host material, the amount of host material used is the mass obtained by adding the amount of the hole-transporting host material used and the amount of the electron-transporting host material used. The mass ratio of the hole-transporting host material and the electron-transporting host material may be 1:9 to 9:1, preferably 4:6 to 6:4, and more preferably approximately 1:1.

The amount of emitting dopant used varies depending on the type of emitting dopant, and can be determined according to its characteristics. The standard for the usage amount of the emitting dopant is preferably 0.001 to 50% by mass, more preferably 0.05 to 20% by mass, and even more preferably 0.1 to 10% by mass of the total mass of the light emitting layer material. The above range is preferable because, for example, concentration quenching phenomenon can be prevented.

When an assisting dopant material is used, the standards for the usage amounts of the host material, assisting dopant material, and emitting dopant material are 40 to 99% by mass and 59 to 1% by mass, respectively, based on the total mass of the light emitting layer material. and 20 to 0.001 mass%, preferably 60 to 95 mass%, 39 to 5 mass% and 10 to 0.01 mass%, respectively, more preferably 70 to 90 mass%, 29 to 10 mass% and It is 5 to 0.05 mass%.

The polycyclic aromatic compound of the present invention is more preferably used as a material for forming a light-emitting layer, and is particularly preferably used as a dopant.

A polycyclic aromatic compound having a structure containing a structural unit represented by Formula (1) or Formula (2) is a “thermally activated delayed phosphor” and is an organic EL device that exhibits thermally activated delayed fluorescence (TADF) (hereinafter referred to as “thermally activated delayed phosphor”). It may also be used as an emitting dopant for a “TADF device”. In a “thermally activated delayed phosphor”, by reducing the energy difference between the lowest singlet excitation state and the lowest triplet excitation state, reverse intersystem crossing from the lowest triplet excitation state, which usually has a low transition probability, to the lowest singlet excitation state is achieved. It is generated with high efficiency, and light emission from a singlet (thermally activated delayed fluorescence, TADF) is expressed. In normal fluorescence emission, 75% of the triplet excitons generated by current excitation pass through the heat deactivation path and cannot be extracted as fluorescence. On the other hand, in TADF, all excitons can be used for fluorescence emission, and a highly efficient organic EL device can be realized.

The polycyclic aromatic compound having a structure containing the structural unit expressed by formula (1) or formula (2) is an emitting dopant of a “TADF device,” an emitting dopant of a TADF device using two types of hosts, and a separate dopant. An emitting dopant for an organic electroluminescent device (TAF device) using a thermally activated delayed phosphor as an assisting dopant, an organic electroluminescent device using a phosphorescent material as an assisting dopant (phosphor-sensitized assist device) It can be used as an emitting dopant for fluorescent devices and PSF devices. From the viewpoint that the smaller the material used in the device, the easier it is to manufacture, it is preferable to use it as an emitting dopant for a TADF device using two types of TADF device emitting dopants or hosts, with the former being more preferable. From the viewpoint of efficiency, it is preferable to use it as an emitting dopant of a TAF device and an emitting dopant of a phosphorescent assist device, and it is more preferable to use it as an emitting dopant of a TAF device.

In general, fast delayed fluorescence is considered to have excellent TADF properties. Specifically, when a light-emitting material with a delayed fluorescence lifetime of 100 μsec or less is used as an emitting dopant in a light-emitting device, high device efficiency and a long device life can be provided. The delayed fluorescence lifetime is preferably less than 20 μsec, more preferably 10 μsec or less, and most preferably 5 μsec or less.

Additionally, generally, the smaller the value of ΔE _S1T1 , the better the TADF properties. Meanwhile, △E _S1T1 is the energy difference between the lowest singlet excited energy level (E _S1 ) and the lowest triplet excited energy level (E _T1 ). Specifically, the value of ΔE _S1T1 is preferably 0.20 eV or less, more preferably 0.15 eV or less, and especially preferably 0.10 eV or less.

<Host material>

As host materials, condensed ring derivatives such as anthracene and pyrene, which were previously known as light emitters, bistyryl derivatives such as bistyryl anthracene derivatives and distyrylbenzene derivatives, tetraphenylbutadiene derivatives, cyclopentadiene derivatives, fluorene derivatives, Benzofluorene derivatives, N-phenylcarbazole derivatives, carbazonitrile derivatives, etc. can be mentioned.

The lowest triplet excitation energy level (E _T1 ) of the host material is higher than the E _T1 of the dopant or assisting dopant with the highest E _T1 in the light-emitting layer from the viewpoint of promoting rather than inhibiting the generation of TADF in the light-emitting layer. It is preferable that it is high, and specifically, the E _T1 of the host material is preferably higher by 0.01 eV or more, more preferably by 0.03 eV or more, and higher by 0.1 eV or more compared to the E _T1 of the above-mentioned dopant or assisting dopant. It is more desirable than Additionally, E _T1 of the host material is preferably 2.55 eV or more, more preferably 2.58 eV or more, and even more preferably 2.65 eV or more.

A compound with TADF activity may be used as the host material.

There may be one type of host material, or a combination of multiple types may be used. In the case of a plurality of combinations, it is preferable that it is a combination of a hole-transporting host material and an electron-transporting host material.

The hole-transporting host material (HH) and the electron-transporting host material (EH) satisfy the following relationships with respect to HOMO (Highest Occupied Molecular Orbital) and LUMO (Lowest Unoccupied Molecular Orbital).

The HOMO of the hole-transporting host material (HH) is shallower than the HOMO of the electron-transporting host material (EH), and the LUMO of the electron-transporting host material (EH) is deeper than the LUMO of the hole-transporting host material (HH).

Additionally, it is preferable that the HOMO of the emitting dopant is shallower than the HOMO of the hole-transporting host material (HH), or that the LUMO of the emitting dopant is deeper than the LUMO of the electron-transporting host material (EH).

In addition, the lowest triplet excitation energy level (E _T1 ) of the hole-transporting host material (HH) and the electron-transporting host material (EH) is the lowest in the light-emitting layer from the viewpoint of promoting rather than inhibiting the generation of TADF in the light-emitting layer. It is preferable that E _T1 of the emitting dopant or assisting dopant having high ET1 is high, and specifically, E _T1 of the host material is 0.01 eV or more compared to E _T1 of the emitting dopant or assisting dopant. It is preferable that it is high, it is more preferable that it is 0.03 eV or more high, and it is still more preferable that it is 0.1 eV or more high. Additionally, E _T1 of the host material is preferably 2.47 eV or more, more preferably 2.49 eV or more, and still more preferably 2.56 eV or more.

Additionally, it is preferable to use a hole-transporting host material in the hole-transporting layer adjacent to the light-emitting layer, and to use an electron-transporting host material in the electron-transporting layer adjacent to the light-emitting layer. This is because carrier leakage and energy leakage from the light-emitting layer to adjacent layers become less likely to occur, and a highly efficient organic EL device can be obtained. The host material (hole-transporting host material) in the light-emitting layer and the hole-transporting layer material may be the same or different. In addition, the host material (electron-transporting host material) in the light-emitting layer and the material of the electron-transporting layer may be the same or different.

[Hole transporting host material (HH)]

Examples of a preferred hole-transporting host material (HH) include at least one selected from the group consisting of an aryl ring and a heteroaryl ring, which is represented by the formula (HH-1), or has a partial structure represented by the formula (HH-1). Examples include compounds having a structure containing three rings. This compound preferably does not contain any imine structure (-N=C-; including the partial structure of the heteroaryl ring), boron (>B-), and cyano (CN).

In formula (HH-1),

Q is >O, >S, or >NA ^H ,

One carbon atom next to the carbon atom bonded to Q in each of the two phenyls in the formula (HH-1) may be bonded to each other with L,

L is a single bond, >O, >S, or >C(-A ^H ) ₂ ,

A ^H is hydrogen, aryl, or heteroaryl, and two A ^H in >C(-A ^H ) ₂ may be bonded to each other.

When the hole-transporting host material contains the structure represented by formula (HH-1) as a partial structure, it may contain one partial structure, but it is also preferable that it contains two or more partial structures. When two or more are included, the partial structures of the two or more may be the same or different from each other. Two or more partial structures may be bonded to each other by a single bond, may be bonded by sharing any ring contained in the partial structure, or may be bonded by condensing any rings contained in the partial structure. The partial structure may further have a substituent selected from aryl, heteroaryl, diarylamino, or aryloxy.

The compound represented by the above formula (HH-1) or having a partial structure represented by the formula (HH-1) has a structure containing at least three rings selected from the group consisting of an aryl ring and a heteroaryl ring. have The number of rings included is preferably 6 or more, and more preferably 8 or more. Additionally, it is preferably 20 or less, more preferably 15 or less, and even more preferably 10 or less. The number of rings means the number as a single ring, and for a condensed ring, the number is the number of monocycles constituting the condensed ring.

The hole-transporting host material includes at least one partial structure selected from the group consisting of a triarylamine structure, a carbazole ring, a dibenzofuran ring, a dibenzothiophene ring, and a phenoxazine or phenothiazine-containing condensed polycycle. It is preferable that it is a compound that The hole-transporting host material may contain one such partial structure, but may preferably contain two or more such partial structures. When two or more are included, the partial structures of the two or more may be the same or different from each other.

Specific examples of hole-transporting host materials include the following compounds.

Among the above, HH-1-1, HH-1-2, HH-1-4 to HH-1-12, HH-1-17, HH-1-18, HH-1-20 to HH-1-24 , HH-1-82, HH-1-84~HH-1-89, HH-1-91, HH-1-92, HH-1-106~HH-1-108 and HH-1-109~HH -1-113 is preferred.

[Electron transporting host material (EH)]

As an example of an electron transporting host material (EH),

It is represented by the formula (EH-1A) to (EH-1D), or has a partial structure represented by the formula (EH-1A) to (EH-1D), and has at least one selected from the group consisting of an aryl ring and a heteroaryl ring. Examples include compounds having a structure containing three rings.

In formulas (EH-1A) to (EH-1D),

Ar is a heteroaryl ring containing N=C as a partial structure constituting the ring,

Z is a single bond, -O-, -S-, or -N(-A ^E )-,

The carbon atom next to the bonded carbon atom of Z and A ^E bonded to Z may be bonded to each other by L,

L is a single bond, >O, >S or >C(-A ^E ) ₂ ,

A ^E is aryl, heteroaryl, or triarylsilyl, and two A ^E 's in >C(-A ^E ) ₂ may be bonded to each other,

X is C, P or S,

When X is C, n=2, m=1,

When X is P, n=3, m=1,

When X is S, n=2, m=1~2.

Compounds having the above formulas (EH-1A) to (EH-1D) or partial structures represented by formulas (EH-1A) to (EH-1D) are selected from the group consisting of aryl rings and heteroaryl rings. It has a structure containing at least three rings. The number of rings included is preferably 4 or more, more preferably 6 or more, and even more preferably 8 or more. Additionally, it is preferably 20 or less, more preferably 15 or less, and even more preferably 10 or less. The number of rings means the number as a single ring, and for a condensed ring, the number is the number of monocycles constituting the condensed ring.

When the electron-transporting host material contains the structures represented by formulas (EH-1A) to (EH-1D) as partial structures, it may contain one partial structure, but it is also preferable to contain two or more of these partial structures. When two or more are included, the partial structures of the two or more may be the same or different from each other. Two or more partial structures may be bonded to each other by a single bond, may be bonded by sharing any ring contained in the partial structure, or may be bonded so that arbitrary rings contained in the partial structure are condensed. The partial structure may further have a substituent selected from aryl, heteroaryl, diarylamino, or aryloxy.

Specific examples of electron-transporting host materials include the following compounds.

As another preferred example of the electron-transporting host material (a compound having a partial structure represented by formula (EH-1)), a polycyclic aromatic compound represented by the formula (EH-1b) below, or a compound represented by the formula (EH-1b) below: Examples include multimers of polycyclic aromatic compounds having multiple structures.

In formula (EH-1b),

R ¹ , R ² , R ³ , R ⁴ and R ⁵ (hereinafter also referred to as “R ¹ etc.”) are each independently hydrogen or a substituent. This substituent may be selected from the substituent group Z.

In the formula (EH-1b), X ¹ and X ² are each independently >NR (amine nitrogen), >O, >C(-R ⁾ ₂ , >S or >Se, and There is no case where ² together becomes >C(-R) ₂ ,

R in the >NR and >C(-R) ₂ is each independently hydrogen or a substituent selected from the substituent group Z, and may be further selected from aryl, heteroaryl, alkyl, or cycloalkyl (above, second substituent). It may be substituted, and R of >NR and >C(-R) ₂ may each independently be bonded to at least one of the a ring, b ring, and c ring through a linking group or single bond.

Y ¹ , Y ² , Y ³ , Y ⁴ , Y ⁵ and Y ⁶ (hereinafter also referred to as “Y ¹ etc.”) are each independently =C(-R)- or =N- (pyridine nitrogen) and at least one is =N- (pyridine nitrogen).

R in =C(-R)- is each independently hydrogen or a substituent selected from the substituent group Z.

Adjacent groups among R ¹ , R ² , R ³ , R ⁴ and R ⁵ , and =C(-R)- as Y ¹ to Y ⁶ combine to form a ring, b ring and c ring. may form an aryl ring or heteroaryl ring together with at least one ring, and at least one hydrogen in the formed ring is aryl, heteroaryl, diarylamino, diheteroarylamino, arylheteroarylamino, diaryl. It may be substituted with boryl (two aryls may be bonded through a single bond or linking group), alkyl, cycloalkyl, alkoxy, or aryloxy (above, first substituent), and at least one hydrogen in these is aryl. , heteroaryl, alkyl, or cycloalkyl (above, second substituent) may be further substituted.

At least one hydrogen in the compound and structure represented by formula (EH-1b) may be substituted with cyano, halogen, or deuterium.

In formula (EH-1b), R ¹ , R ² , R ³ , R ⁴ and R ⁵ are all hydrogen, or R ³ and R ⁴ are both hydrogen and R ¹ , R ² and R ⁵ It is preferable that any one or more selected from the group consisting of substituents other than hydrogen are substituents other than hydrogen, and the others are hydrogen. The substituent is preferably aryl, which may be substituted with alkyl or heteroaryl, heteroaryl which may be substituted with alkyl or aryl, or diarylamino which may be substituted with alkyl or aryl. At this time, the alkyl is preferably an alkyl with 1 to 6 carbon atoms (methyl, t-butyl, etc.), the aryl is preferably phenyl or biphenyl, and the heteroaryl is triazinyl or carbazolyl (2-carbazolyl). , 3-carbazolyl, 9-carbazolyl, etc.), pyrimidinyl, pyridinyl, dibenzofuranyl or dibenzothienyl. Specific examples include phenyl, biphenyl, diphenyltriazinyl, carbazolyltriazinyl, monophenylpyrimidinyl, diphenylpyrimidinyl, carbazolyltriazinyl, pyridinyl, dibenzofuranyl and dibenzothienyl. I can hear it.

Y ¹ and the like are each independently =C(-R)- or =N-, and at least one is =N-. Any of Y ¹ to Y ⁶ may be =N-. Preferably, Y ¹ and Y ⁶ are =N- (a ring is a pyrimidine ring), Y ¹ and Y ⁶ are =N- (a ring is a pyridine ring), Y ² and Y ⁵ are =N- (b ring and c ring is a pyridine ring), Y ³ and Y ⁴ are =N- (b ring and c ring are pyridine ring), Y ² to Y ⁵ are =N- (b ring and c ring are pyrimidine ring), Y ¹ , Y ³ , Y ⁴ and Y ⁶ are =N- (ring a is a pyrimidine ring, ring b and ring c are pyridine rings), Y ¹ , Y ² , Y ⁵ and Y ⁶ are =N- (ring a is a pyrimidine ring, ring b and c ring is a pyridine ring), Y ¹ to Y ⁶ are =N- (a ring, b ring and c ring are pyrimidine ring), Y ² or Y ⁵ is =N- (b ring or c ring is pyridine ring).

Furthermore, in addition to the above configuration relationship of =N-, it is preferable that X ¹ and X ² are >O, and a polycyclic aromatic compound containing a partial structure represented by any of the following formulas is preferable.

In particular, the polyaromatic compound containing the partial structure represented by the formula (EH-1b-N1) has high E _S1 , high E _T1 , and small ΔE _S1T1 compared to the structure without N.

Specific examples of the polycyclic aromatic compound represented by formula (EH-1b) are shown below.

Among the above, EH-1-1 to EH-1-4, EH-1-10, EH-1-21 to EH-1-25, EH-1-32, EH-1-33, EH-1-51 ~EH-1-59, EH-1-61, EH-1-66, EH-1-68, EH-1-71, EH-1-72, EH-1-90, EH-1-94~EH -1-98, EH-1-100, EH-1-101, EH-1-104, EH-1-115, EH-1-117, EH-1-120, EH-1-122, EH-1 -123, EH-1-127 to EH-1-130 are preferred.

[Combination of hole-transporting host material and electron-transporting host material]

The combination of the hole-transporting host material and the electron-transporting host material is selected by the HOMO, LUMO, and lowest excitation triplet energy level (E _T1 ) of the hole-transporting host material, electron-transporting host material, and dopant material.

Regarding HOMO and LUMO, the HOMO(HH) of the hole-transporting host material is shallower than the HOMO(EH) of the electron-transporting host material, and the LUMO(EH) of the electron-transporting host material is deeper than the LUMO(HH) of the hole-transporting host material. Select a combination, and more specifically, it is preferable that HOMO(HH) is 0.10 eV or more shallower than HOMO(EH), LUMO(HH) is 0.10 eV or more deeper than HOMO(EH), and HOMO(HH) is 0.10 eV or more shallower than HOMO(EH). A combination that is more than 0.20 eV shallower than (EH), LUMO(HH) is more than 0.20 eV deeper than HOMO(EH), is more preferable, HOMO(HH) is more than 0.25 eV shallower than HOMO(EH), and LUMO(HH) is more than 0.25 eV shallower than HOMO(EH). A combination deeper than (EH) by 0.25 eV or more is more preferable.

The hole-transporting host material and the electron-transporting host material may be combined to form an association called an exciplex. It is generally known that exiplexes are easy to form between materials with a relatively deep LUMO level and materials with a shallow HOMO level. The interaction of the hole-transporting host material and the electron-transporting host material, specifically whether or not an exciplex is formed, is determined by forming a monolayer film composed of only the hole-transporting host material and the electron-transporting host material under the same conditions as the formation conditions of the light-emitting layer. The spectrum (fluorescence, phosphorescence spectrum) can be measured, and the obtained emission spectrum can be judged by comparing the emission spectra shown individually by the hole-transporting host material and the electron-transporting host material. It can be judged by whether the spectrum of the mixed film containing the hole-transporting host material and the electron-transporting host material shows an emission wavelength that is different from either the spectrum of the film of the hole-transporting host material or the spectrum of the film of the electron-transporting host material. Specifically, an indicator may be that the peak wavelengths of the spectra differ by more than 10 nm.

Specific examples of combinations of a hole-transporting host material and an electron-transporting host material that do not form an exciplex include the following combinations. In order to satisfy the physical properties of HOMO, LUMO, and E _T1 above, in the hole transporting host material, carbazole, dibenzofuran, dibenzothiophene, triarylamine, indolocarbazole, and benzoxazinophenoxazine are partially used. Compounds having carbazole, dibenzofuran, and dibenzothiophene as partial structures are preferable, and compounds having carbazole as partial structures are still more preferable. Likewise, for the electron-transporting host material, compounds having pyridine, triazine, phosphine oxide, benzofuropyridine, and dibenzoxacillin as partial structures are preferred, and triazine, phosphine oxide, benzopyridine, and dibenzoxacillin are preferred. Compounds having siline as a partial structure are more preferable, and compounds having triazine are still more preferable.

More specifically, the hole transport host material is HH-1-1, HH-1-2, HH-1-4 to HH-1-12, HH-1-17, HH-1-18, HH-1 -20~HH-1-24, HH-1-82, HH-1-84~HH-1-89, HH-1-91, HH-1-92, and HH-1-106~HH-1- It is preferably selected from the group consisting of 108, and the electron transport host material is EH-1-1 to EH-1-4, EH-1-10, EH-1-21 to EH-1-25, EH-1 -32, EH-1-33, EH-1-51~EH-1-59, EH-1-61, EH-1-71, EH-1-72, EH-1-90, EH-1-100 , EH-1-101, EH-1-104, EH-1-117, EH-1-120, EH-1-122, EH-1-123, and EH-1-127 through EH-1-130. It is preferable to select from the group consisting of: Preferred examples of the combination include compound HH-1-1 and compound EH-1-22, compound HH-1-1 and compound EH-1-23, compound HH-1-1 and compound EH-1-24, and compound HH- 1-2 and Compound EH-1-22, Compound HH-1-2 and Compound EH-1-23, Compound HH-1-2 and Compound EH-1-24, or Compound HH-1-1 and Compound EH- It can be 1-128.

Specific examples of the combination of a hole-transporting host material and an electron-transporting host material forming an exciplex include the following combinations. In order to satisfy the above physical property values of HOMO, LUMO and E _T1 , in the hole transporting host material, compounds having carbazole, triarylamine, indolocarbazole and benzoxazinophenoxazine as partial structures are preferred, and triarylamine Compounds having arylamine, indolocarbazole, and benzoxazinophenoxazine as partial structures are more preferable, and compounds having triarylamine as partial structures are still more preferable. Similarly, for the electron-transporting host material, compounds having pyridine, triazine, phosphine oxide, and benzofuropyridine as partial structures are preferable, and compounds having triazine, phosphine oxide, benzopyridine, and dibenzoxacillin as partial structures are preferable. Compounds having phosphine oxide and triazine are more preferable.

More specifically, the hole transporting host material is HH-1-1, HH-1-2, HH-1-11, HH-1-12, HH-1-17, HH-1-18, HH-1 It is preferably selected from the group consisting of -23 and HH-1-24, and the electron transport host material is EH-1-1 to EH-1-4, EH-1-21 to EH-1-25, EH- 1-51~EH-1-57, EH-1-59, EH-1-66, EH-1-68, EH-1-90, EH-1-94, EH-1-100, EH-1- 101, EH-1-104, EH-1-117, EH-1-120, EH-1-122, EH-1-123, and EH-1-127 to EH-1-130. It is desirable. Preferred examples of the combination include compound HH-1-1 and compound EH-1-21, compound HH-1-2 and compound EH-1-21, compound HH-1-12 and compound EH-1-94, and compound HH- 1-12 and HH-1-117, Compound HH-1-1 and Compound EH-1-130, Compound HH-1-33 and Compound EH-1-117, Compound HH-1-48 and Compound EH-1- 117 or compound HH-1-49 and compound EH-1-117.

In addition, for specific combinations of hole-transporting host materials and electron-transporting host materials, see Organic Electronics 66 (2019)227-24, Advanced.Functional Materials 25 (2015) 361-366., Advanced Materials 26 (2014) 4730- 4734., ACS Applied Materials and Interfaces 8 (2016) 32984-32991., ACS Applied Materials and Interfaces 2016, 8, 9806-9810, ACS Applied Materials and Interfaces 2016, 8, 32984-32991, Journal of Materials Chemistry C, 2018 , 6, 8784-8792, Angewante Chemie International Edition. 2018, 57, 12380-12384, Advanced Functional Materials, 24, 2014, 3970, Advanced Materials, 26, 2014, 5684, and Synthetic Metals, 201, 2015, 49.

<Assisting dopant (thermally activated delayed phosphor or phosphorescent material)>

The light-emitting layer preferably contains an assisting dopant along with an emitting dopant and a host material. As the assisting dopant, a thermally activated delayed phosphor or phosphorescent material is preferable.

In this embodiment, known host compounds can be used, and examples include compounds having at least one of a carbazole ring and a furan ring, and among them, at least one of furanyl and carbazolyl, and an aryl ring. It is preferable to use a compound in which at least one of lene and heteroarylene is bonded. Specific examples include mCP and mCBP. Additionally, a compound with TADF activity may be used as the host compound. In this aspect, it is also preferable to use a combination of a hole-transporting host material and an electron-transporting host material as the host.

The lowest excitation triplet energy level E(1,T,Sh), obtained from the shoulder on the short wavelength side of the peak of the phosphorescence spectrum of the host compound, is the lowest in the light-emitting layer from the viewpoint of promoting rather than inhibiting the generation of TADF in the light-emitting layer. It is preferable that the lowest triplet excitation energy level of the emitting dopant or assisting dopant having a high lowest triplet excitation energy level is E(2,T,Sh), E(3,T,Sh), and specifically, , the lowest triplet excitation energy level E(1,T,Sh) of the host compound is preferably 0.01 eV or more higher than E(2,T,Sh) and E(3,T,Sh), and 0.03 eV or more. It is more preferable that it is high, and it is even more preferable that it is 0.1 eV or more high.

[Thermally activated delayed phosphor]

“Thermal-activated delayed phosphor” refers to a substance that absorbs heat energy to cause reverse intersystem crossing from the lowest triplet excitation state to the lowest singlet excitation state, and is deactivated by radiation from the lowest singlet excitation state to emit delayed fluorescence. means a compound. However, “thermally activated delayed fluorescence” also includes passing through a higher order triplet in the excitation process from the lowest triplet excited state to the lowest singlet excited state. For example, a paper by Monkman of Durham University (NATURE COMMUNICATIONS, 7:13680, DOI:10.1038/ncomms 13680), a paper by Hosokai of the Institute of Industrial Technology (Hosokai et al., Sci.Adv. 2017; 3 :e1603282), a paper by Sato and others at Kyoto University (Scientific Reports, 7:4820, DOI:10.1038/s41598-017-05007-7), and also a conference presentation by Sato and others at Kyoto University (98th Spring Annual Meeting of the Chemical Society of Japan, Publication number: 2I4-15, Mechanism of highly efficient luminescence in organic electroluminescence using DABNA as a luminescent molecule, Kyoto University Graduate School of Engineering), review by Bui et al. (DOI:10.3762/bjoc.14.18), Duan et al. Reviews (DOI:10.1063/1.5143501), reviews by Dings (DOI:10.1088/1674-4926/42/5/050201), and reviews by Xies (DOI:10.1002/adom.202002204). In the present invention, when the fluorescence lifetime of a sample containing the target compound is measured at 300K, the target compound is determined to be a “heat-activated delayed phosphor” based on the observation of a slow fluorescence component. Here, the slow fluorescence component refers to a fluorescence lifetime of 0.1 μsec or more. Measurement of fluorescence lifetime can be performed, for example, using a fluorescence lifetime measuring device (C11367-01, manufactured by Hamamatsu Photonics Co., Ltd.).

In a light-emitting layer further containing a “thermally activated delayed phosphor” as an assisting dopant, the polycyclic aromatic compound of the present invention can function as an emitting dopant. In other words, the “thermally activated delayed phosphor” can function as an assisting dopant that assists the light emission of the polycyclic aromatic compound of the present invention.

In this specification, an organic electroluminescent device using a thermally activated delayed phosphor as an assisting dopant may be referred to as a “TAF device” (TADF Assisting Fluorescence device).

“Host compound” in a TAF device refers to a compound whose lowest singlet excitation energy level, obtained from the shoulder on the short wavelength side of the peak of the fluorescence spectrum, is higher than that of the heat-activated delayed phosphor as an assisting dopant and the emitting dopant. do.

Figure 2 shows the energy level diagram of the light emitting layer of a TAF device using a general fluorescent dopant as an emitting dopant (ED). In the figure, E(1,G) is the energy level of the ground state of the host, E(1,S,Sh) is the lowest excitation singlet energy level obtained from the shoulder of the short wavelength side of the host's fluorescence spectrum, and E(1,S,Sh) is the short wavelength of the host's phosphorescence spectrum. The lowest excitation triplet energy level obtained from the shoulder on the side is E(1,T,Sh), the ground state energy level of the assisting dopant is E(2,G), and the fluorescence spectrum of the assisting dopant is obtained from the shoulder on the short wavelength side. E(2,S,Sh) is the lowest excitation singlet energy level, E(2,T,Sh) is the lowest triplet excitation energy level obtained from the shoulder of the short wavelength side of the phosphorescence spectrum of the assisting dopant, and E(2,T,Sh) is the lowest excitation triplet energy level of the emitting dopant. E(3,G) is the ground state energy level, E(3,S,Sh) is the lowest excitation singlet energy level obtained from the shoulder on the short-wavelength side of the fluorescence spectrum of the emitting dopant, and E(3,S,Sh) is the short-wavelength side of the phosphorescence spectrum of the emitting dopant. The lowest excitation triplet energy level obtained from the shoulder is E(3,T,Sh), holes are h+, electrons are e-, and fluorescence resonance energy transfer is FRET (Fluorescence Resonance Energy Transfer). In a TAF device, when a general fluorescent dopant is used as an emitting dopant (ED), the energy upconverted from the assisting dopant moves to the lowest excited singlet energy level E(3,S,Sh) of the emitting dopant and emits light. do. However, some of the lowest excitation triplet energy levels E(2,T,Sh) on the assisting dopant move to the lowest excitation triplet energy level E(3,T,Sh) on the emitting dopant, or An intersystem crossing occurs from the singlet excited energy level E(3,S,Sh) to the lowest triplet excited energy level E(3,T,Sh), and continues thermally to the ground state E(3,G). become deactivated by Due to this path, some of the energy is not used for light emission, resulting in energy waste.

In contrast, in the organic electroluminescent device of this embodiment, the energy transferred from the assisting dopant to the emitting dopant can be efficiently used for light emission, and thus high light emission efficiency can be realized. This is presumed to be due to the following light emission mechanism.

FIG. 3 shows a preferable energy relationship in the organic electroluminescent device of this embodiment. In the organic electroluminescent device of this embodiment, a compound having a boron atom as an emitting dopant has a high lowest triplet excitation energy level E(3,T,Sh). For this reason, the lowest excitation singlet energy upconverted in the assisting dopant, for example, crosses intersystemally to the lowest excitation triplet energy level E(3,T,Sh) in the emitting dopant. It is upconverted or recovered to the lowest excited triplet energy level E(2,T,Sh) on the assisting dopant (thermally activated delayed phosphor). Therefore, the generated excitation energy can be used for light emission without waste. In addition, by dividing the molecule into two types that can improve the functions of upconversion and light emission, it is expected that the residence time of high energy will be reduced and the burden on the compound will be reduced.

The thermally activated delayed phosphor (TADF compound) used in TAF devices uses an electron-donating substituent called a donor and an electron-accepting substituent called an acceptor to create HOMO (Highest Occupied Molecular Orbital) and LUMO (Lowest Unoccupied) within the molecule. It is preferable that it is a donor-acceptor type thermally activated delayed phosphor (D-A type TADF compound) designed to localize the molecular orbital and cause efficient reverse intersystem crossing.

Here, in this specification, “electron-donating substituent” (donor) refers to the substituent and partial structure where HOMO is localized in the heat-activated delayed phosphor molecule, and “electron-accepting substituent” (acceptor) refers to heat-activated delayed phosphor molecule. This refers to the substituents and partial structures in which LUMO is localized among active delayed phosphor molecules.

In general, thermally activated delayed phosphors using donors or acceptors have large spin orbit coupling (SOC) due to their structure, and at the same time, the exchange interaction between HOMO and LUMO is small and ΔE _S1T1 is small, Very fast inverse intersystem crossing rates are obtained. On the other hand, thermally activated delayed phosphors using donors or acceptors have greater structural relaxation in the excited state (for some molecules, the stable structures are different in the ground state and excited state, so external stimulation causes the structural relaxation to change from the ground state to the excited state). When the conversion occurs, the structure changes to a stable structure in the excited state) and provides a wide luminescence spectrum, so there is a possibility that color purity may be reduced when used as a luminescent material.

However, by simultaneously using the polycyclic aromatic compound of the present invention, the polycyclic aromatic compound of the present invention functions as an emitting dopant and the TADF material functions as an assisting dopant, and can provide high color purity. The TADF material may be any compound whose emission spectrum overlaps at least part of the absorption spectrum of the polycyclic aromatic compound of the present invention. Both the polyaromatic compound of the present invention and the TADF material may be contained in the same layer, or may be contained in adjacent layers or other adjacent layers.

As a thermally activated delayed phosphor in a TAF element, for example, a compound in which a donor and an acceptor are bonded directly or through a spacer can be used. As the electron donating group (donor structure) and electron accepting group (acceptor structure) used in the thermally activated delayed phosphor of the present invention, for example, the structure described in Chemistry of Materials, 2017, 29, 1946-1963 You can use it. Donor structures include carbazole, dimethylcarbazole, di-tert-butylcarbazole, dimethoxycarbazole, tetramethylcarbazole, benzofluorocarbazole, benzothienocarbazole, phenyldihydroindolocarbazole, Phenylbicarbazole, bicarbazole, tercarbazole, diphenylcarbazolylamine, tetraphenylcarbazolyldiamine, phenoxazine, dihydrophenazine, phenothiazine, dimethyldihydroacridine, diphenylamine, bis. (tert-butyl phenyl)amine, N1-(4-(diphenylamino)phenyl)-N4,N4-diphenylbenzene-1,4-diamine, dimethyltetraphenyldihydroacridinediamine, tetramethyl-dihydroinde Noacridine, diphenyldihydrodibenzoazacillin, etc. are mentioned. Acceptor structures include sulfonyl dibenzene, benzophenone, phenylenebis (phenylmethanone), benzonitrile, isonicotinonitrile, phthalonitrile, isophthalonitrile, paraphthalonitrile, benzene tricarbonitrile, and triazole. , oxazole, thiadiazole, benzothiazole, benzobis(thiazole), benzooxazole, benzobis(oxazole), quinoline, benzoimidazole, dibenzoquinoxaline, heptaazaphenalene, thioxanthone dioxide , dimethylanthracenone, anthracenedione, 5H-cyclopenta[1,2-b:5,4-b']dipyridine, fluorene dicarbonitrile, triphenyltriazine, pyrazine dicarbonitrile, pyrimidine, phenylpyridine Examples include midine, methylpyrimidine, pyridine dicarbonitrile, dibenzoquinoxaline dicarbonitrile, bis(phenylsulfonyl)benzene, dimethylthioxanethene dioxide, thianthrenetetroxide, and tris(dimethylphenyl)borane. In particular, compounds having heat-activated delayed fluorescence in the TAF device have partial structures such as carbazole, phenoxazine, acridine, triazine, pyrimidine, pyrazine, thioxanthene, benzonitrile, phthalonitrile, and isophene. It is preferable that it is a compound having at least one selected from talonitrile, diphenylsulfone, triazole, oxadiazole, thiadiazole and benzophenone.

The compound used as the assisting dopant of the light-emitting layer in the TAF element is a thermally activated delayed phosphor, and is preferably a compound whose emission spectrum overlaps at least partially with the absorption peak of the emitting dopant.

[Phosphorescent material (assisting dopant)]

In the light-emitting layer, a phosphorescent material may be used as an assisting dopant. In the present specification, an organic electroluminescent device using a phosphorescent material as an assisting dopant is sometimes referred to as a phosphorescent assist device: a phosphor-sensitized fluorescent device, or a PSF device. Phosphorescent materials utilize intramolecular spin-orbit interactions (heavy atom effect) with metal atoms to obtain light emission from triplet excited states. As such a phosphorescent material, for example, a luminescent metal complex can be used. Examples of the luminescent metal complex include compounds represented by the following formula (B-1) and the following formula (B-2).

In formula (B-1), M is at least one selected from the group consisting of Ir, Pt, Au, Eu, Ru, Re, Ag and Cu, n is an integer of 1 to 3, and “X-Y” are each independently two-dentate ligands.

In formula (B-2), M is at least one member selected from the group consisting of Pt, Re, and Cu, and “W-X-Y-Z” is a 4-dentate ligand.

In formula (B-1), from the viewpoint of efficiency and life, M is preferably Ir, and n is preferably 3.

In formula (B-2), M is preferably Pt from the viewpoint of efficiency and lifespan.

The ligand (X-Y) in formula (B-1) has at least one ligand selected from the group consisting of the following. The ligand (W-X-Y-Z) in formula (B-2) has as part of at least one ligand selected from the group consisting of the following.

During the ceremony,

--- combines with the central metal M,

Y is, each independently, BR _e , NR _e , PR _e , O, S, Se, C=O, S=O, SO2, CR _e R _f , SiR _e R _f , or GeR _e R _f

The aromatic carbons C-H in the ring may each independently be substituted with N,

R _e and R _f may be arbitrarily condensed or combined to form a ring,

R _a , R _b , R _c , and R _d may each independently be unsubstituted or substituted from 1 to the maximum number of possible substitutions,

R _a , R _b , R _c , R _d , R _e , and R _f are each independently hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, alkenyl , cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, or a combination thereof,

However, any two adjacent substituents in R _a , R _b , R _c , and R _d may condense or combine to form a ring, or may form a multidentate ligand.

Examples of compounds represented by formula (B-1) include Ir(ppy) ₃ , Ir(ppy) ₂ (acac), Ir(mppy) ₃ , Ir(PPy) ₂ (m-bppy), and BtpIr( acac), Ir(btp) ₂ (acac), Ir(2-phq) ₃ , Hex-Ir(phq) ₃ , Ir(fbi) ₂ (acac), fac-Tris(2-(3-p-xylyl) phenyl)pyridine iridium(III), Eu(dbm) ₃ (Phen), Ir(piq) ₃ , Ir(piq) ₂ (acac), Ir(Fliq) ₂ (acac), Ir(Flq) ₂ (acac), Ru(dtb-bpy) ₃ 2(PF ₆ ), Ir(2-phq) ₃ , Ir(BT) ₂ (acac), Ir(DMP) ₃ , Ir(Mphq) ₃ IR(phq) ₂ tpy, fac -Ir(ppy) ₂ Pc, Ir(dp)PQ ₂ , Ir(Dpm)(Piq) ₂ , Hex-Ir(piq) ₂ (acac), Hex-Ir(piq) ₃ , Ir(dmpq) ₃ , Ir (dmpq) ₂ (acac), FPQIrpic, etc.

Other compounds represented by formula (B-1) include, for example, the following compounds.

In addition, Japanese Patent Application Laid-Open No. 2006-089398, Japanese Patent Application Publication No. 2006-080419, Japanese Patent Application Laid-Open No. 2005-298483, Japanese Patent Application Laid-Open No. 2005-097263, Japanese Patent Application Laid-Open No. 2004-111379, and US Patents Iridium complex described in Application Publication No. 2019/0051845, etc., or Advanced Materials, 26:7116-7121, NPG Asia Materials 13, 53 (2021), Applied Physics Letters, 117, 253301 (2020), Light-Emitting Diode- The platinum complex described in An Outlook On the Empirical Features and Its Recent Technological Advancements, Chapter 5 may also be used.

<Other dopant materials>

The above emitting dopant may be used in combination with other dopant materials. However, the other dopant material is preferably less than 100% by mass, more preferably 50% by mass or less, even more preferably 30% by mass or less, relative to the total mass of the emitting dopant in one light emitting layer. It is particularly preferable that it is % or less. As other dopant materials, known compounds can be used, and various materials can be selected depending on the desired emission color. Specifically, for example, condensed ring derivatives such as phenanthrene, anthracene, pyrene, tetracene, pentacene, perylene, naphthopyrene, dibenzopyrene, rubrene, and chrysene, benzoxazole derivatives, and benzothiazole. Derivatives, benzoimidazole derivatives, benzotriazole derivatives, oxazole derivatives, oxadiazole derivatives, thiazole derivatives, imidazole derivatives, thiadiazole derivatives, triazole derivatives, pyrazoline derivatives, stilbene derivatives, thiophene derivatives, Tetraphenylbutadiene derivatives, cyclopentadiene derivatives, bistyryl derivatives such as bistyryl anthracene derivatives and distyrylbenzene derivatives (Japanese Patent Application Laid-open No. 1-245087), bistyrylarylene derivatives (Japanese Patent Application Laid-Open No. 2) -247278 Publication), diazindacene derivatives, furan derivatives, benzofuran derivatives, phenylisobenzofuran, dimethylisobenzofuran, di(2-methylphenyl)isobenzofuran, di(2-trifluoromethylphenyl)iso Isobenzofuran derivatives such as benzofuran and phenylisobenzofuran, dibenzofuran derivatives, 7-dialkylaminocoumarin derivatives, 7-piperidinocoumarin derivatives, 7-hydroxycoumarin derivatives, 7-methoxycoumarin derivatives, 7 -Coumarin derivatives such as acetoxycoumarin derivatives, 3-benzothiazolylcoumarin derivatives, 3-benzoimidazolylcoumarin derivatives, and 3-benzooxazolylcoumarin derivatives, dicyanomethylene pyran derivatives, dicyanomethylenethiopyran derivatives, polymethine Derivatives, cyanine derivatives, oxobenzoanthracene derivatives, xanthene derivatives, rhodamine derivatives, fluorescein derivatives, pyrylium derivatives, carbostyryl derivatives, acridine derivatives, oxazine derivatives, phenylene oxide derivatives, quinacridone derivatives, Quinazoline derivatives, pyrrolopyridine derivatives, furopyridine derivatives, 1,2,5-thiadiazolopyrene derivatives, pyromethene derivatives, perinone derivatives, pyrrolopyrrole derivatives, squaryllium derivatives, biolanthrone derivatives, phenazine Derivatives, acridone derivatives, deazaflavin derivatives, fluorene derivatives, benzofluorene derivatives, etc. may be mentioned.

As another dopant material, it is also preferable to use a polycyclic aromatic compound containing boron described in paragraphs 0097 to 0269 of International Publication No. 2015/102118, International Publication No. 2020/162600, and Japanese Patent Application Publication No. 2021-077890.

2-1-6. abandonment electric field radiation in the device former injection layer , former transport layer

The electron injection layer 107 serves to efficiently inject electrons moving from the cathode 108 into the light emitting layer 105 or the electron transport layer 106. The electron transport layer 106 serves to efficiently transport electrons injected from the cathode 108 or electrons injected from the cathode 108 through the electron injection layer 107 to the light emitting layer 105. The electron transport layer 106 and the electron injection layer 107 are formed by laminating or mixing one or two or more types of electron transport/injection material, or a mixture of an electron transport/injection material and a polymer binder, respectively.

The electron injection/transport layer is a layer that injects electrons from the cathode and is responsible for transporting the electrons. It is desirable that the electron injection efficiency is high and the injected electrons are transported efficiently. For this purpose, it is desirable to use a material that has high electron affinity, high electron mobility, excellent stability, and that impurities that become traps are unlikely to be generated during production and use. However, when considering the transport balance between holes and electrons, if it mainly plays a role in efficiently preventing holes from the anode from flowing to the cathode without recombining, even if the electron transport ability is not very high, it improves luminous efficiency. The effect is equivalent to that of materials with high electron transport capacity. Therefore, the electron injection/transport layer in the present embodiment may also include a function of a layer that can efficiently prevent the movement of holes.

The material (electron transport material) forming the electron transport layer 106 or the electron injection layer 107 includes compounds conventionally used as electron transport compounds in photoconductive materials, and compounds used in the electron injection layer and electron transport layer of organic EL devices. It can be used by arbitrarily selecting from among known compounds in use.

Materials used in the electron transport layer or electron injection layer include compounds made of an aromatic ring or heteroaromatic ring composed of one or more atoms selected from carbon, hydrogen, oxygen, sulfur, silicon, and phosphorus, pyrrole derivatives and condensed ring derivatives thereof, and It is preferable to contain at least one type selected from metal complexes having electron-accepting nitrogen. Specifically, condensed ring aromatic ring derivatives such as naphthalene and anthracene, styryl aromatic ring derivatives such as 4,4'-bis(diphenylethenyl)biphenyl, perinone derivatives, coumarin derivatives, and naphthalimide derivatives. , quinone derivatives such as anthraquinone and diphenoquinone, phosphine oxide derivatives, arylnitrile derivatives, and indole derivatives. Examples of metal complexes having electron-accepting nitrogen include hydroxyazole complexes such as hydroxyphenyloxazole complex, azomethine complex, tropolone metal complex, flavonol metal complex, and benzoquinoline metal complex. These materials can be used alone, but may be mixed with other materials.

Additionally, specific examples of other electron transfer compounds include pyridine derivatives, naphthalene derivatives, anthracene derivatives, phenanthroline derivatives, perinone derivatives, coumarin derivatives, naphthalimide derivatives, anthraquinone derivatives, diphenoquinone derivatives, and diphenylquinone. Derivatives, perylene derivatives, oxadiazole derivatives (1,3-bis[(4-t-butyl phenyl)1,3,4-oxadiazolyl]phenylene, etc.), thiophene derivatives, triazole derivatives (N- (naphthyl-2,5-diphenyl-1,3,4-triazole, etc.), thiadiazole derivatives, metal complexes of auxin derivatives, quinolinol-based metal complexes, quinoxaline derivatives, polymers of quinoxaline derivatives, benzazoles Compounds, gallium complex, pyrazole derivative, perfluorinated phenylene derivative, triazine derivative, pyrazine derivative, benzoquinoline derivative (2,2'-bis(benzo[h]quinolin-2-yl)-9,9' -spirofluorene, etc.), imidazopyridine derivatives, borane derivatives, benzoimidazole derivatives (tris(N-phenylbenzoimidazol-2-yl)benzene, etc.), benzoxazole derivatives, benzothiazole derivatives, quinoline derivatives, Oligopyridine derivatives such as terpyridine, bipyridine derivatives, terpyridine derivatives (1,3-bis (2,2':6',2"-terpyridin-4'-yl)benzene, etc.), naphthyridine derivatives (bis) (1-naphthyl)-4-(1,8-naphthyridin-2-yl)phenyl phosphine oxide, etc.), aldazine derivatives, carbazole derivatives, indole derivatives, phosphine oxide derivatives, bistyryl derivatives, etc. I can hear it.

Additionally, a metal complex having an electron-accepting nitrogen can also be used, for example, a quinolinol-based metal complex, a hydroxyazole complex such as a hydroxyphenyloxazole complex, an azomethine complex, a tropolone metal complex, or a flavonol metal complex. and benzoquinoline metal complexes.

The above-mentioned materials can be used alone, but may also be used in combination with other materials.

Among the above-mentioned materials, borane derivatives, pyridine derivatives, fluoranthene derivatives, BO-based derivatives, anthracene derivatives, benzofluorene derivatives, phosphine oxide derivatives, pyrimidine derivatives, arylnitrile derivatives, triazine derivatives, benzimidazole derivatives, Phenanthroline derivatives and quinolinol-based metal complexes are preferred.

<Reducing substances>

The electron transport layer or electron injection layer may further contain a substance capable of reducing the material forming the electron transport layer or electron injection layer. This reducing substance can be a variety of substances as long as it has a certain reducing property, for example, an alkali metal, an alkaline earth metal, a rare earth metal, an oxide of an alkali metal, a halide of an alkali metal, an oxide of an alkaline earth metal, At least one selected from the group consisting of halides of alkaline earth metals, oxides of rare earth metals, halides of rare earth metals, organic complexes of alkali metals, organic complexes of alkaline earth metals and organic complexes of rare earth metals can be preferably used. .

Preferred reducing substances include alkali metals such as Na (work function 2.36 eV), K (2.28 eV), Rb (2.16 eV), or Cs (1.95 eV), Ca (2.9 eV), and Sr (2.0 eV). alkaline earth metals such as (~2.5 eV) or Ba (copper, 2.52 eV), and materials with a work function of 2.9 eV or less are particularly preferred. Among these, more preferable reducing substances are alkali metals of K, Rb or Cs, even more preferably Rb or Cs, and most preferable is Cs. These alkali metals have a particularly high reducing ability, and by adding a relatively small amount to the material forming the electron transport layer or electron injection layer, the luminance of the organic EL device can be improved and its lifespan can be improved. In addition, as a reducing material with a work function of 2.9 eV or less, a combination of two or more alkali metals is also preferable, especially a combination containing Cs, for example, Cs and Na, Cs and K, Cs and Rb, or Cs. A combination of Na and K is preferred. By including Cs, the reducing ability can be efficiently exerted, and by adding it to the material forming the electron transport layer or the electron injection layer, the luminance of the organic EL device can be improved and its lifespan can be improved.

2-1-7. Cathode in organic electroluminescent device

The cathode 108 serves to inject electrons into the light emitting layer 105 through the electron injection layer 107 and the electron transport layer 106.

The material forming the cathode 108 is not particularly limited as long as it is a material that can efficiently inject electrons into the organic layer, but the same material as the material forming the anode 102 can be used. Among them, metals such as tin, indium, calcium, aluminum, silver, copper, nickel, chromium, gold, platinum, iron, zinc, lithium, sodium, potassium, cesium and magnesium, or their alloys (magnesium-silver alloy, magnesium-silver alloy) Indium alloys, aluminum-lithium alloys such as lithium fluoride/aluminum, etc.) are preferable. In order to improve device characteristics by increasing electron injection efficiency, alloys containing lithium, sodium, potassium, cesium, calcium, magnesium, or these low work function metals are effective. However, these low work function metals are generally unstable in the atmosphere. To improve this problem, there is a known method of using a highly stable electrode by doping a small amount of lithium, cesium or magnesium into the organic layer, for example. As other dopants, inorganic salts such as lithium fluoride, cesium fluoride, lithium oxide, and cesium oxide can also be used. However, it is not limited to these.

Furthermore, to protect the electrode, metals such as platinum, gold, silver, copper, iron, tin, aluminum and indium, or alloys using these metals, inorganic substances such as silica, titania and silicon nitride, polyvinyl alcohol, vinyl chloride, and hydrocarbons. Laminating a polymer compound or the like is a preferred example. The manufacturing method of these electrodes is not particularly limited as long as conduction can be achieved, such as resistance heating, electron beam evaporation, sputtering, ion plating, and coating.

2-1-8. Manufacturing method of organic electroluminescent device

Each layer constituting the organic EL device is formed by forming the material constituting each layer into a thin film using methods such as vapor deposition, resistance heating deposition, electron beam deposition, sputtering, molecular stacking, printing, spin coating or casting, and coating methods. By doing so, it can be formed. There is no particular limitation on the film thickness of each layer formed in this way, and it can be set appropriately depending on the properties of the material, but is usually in the range of 2 nm to 5000 nm. The film thickness can usually be measured with a crystal oscillation type film thickness measuring device or the like. When thinning a film using a vapor deposition method, the deposition conditions vary depending on the type of material, the target crystal structure and association structure of the film, etc. Deposition conditions are generally boat heating temperature +50 to +400℃, vacuum degree of 10 ^-6 to 10 ^-3 Pa, deposition rate of 0.01 to 50nm/sec, substrate temperature of -150 to +300℃, film thickness of 2nm to 5㎛. It is desirable to set it appropriately within the range.

When applying a direct current voltage to the organic EL device obtained in this way, the anode should be + and the cathode should be applied with the polarity of -. When a voltage of about 2 to 40 V is applied, the transparent or translucent electrode side (anode or cathode) can be applied. , and both sides) can be observed. Additionally, this organic EL element emits light even when pulse current or alternating current is applied. Additionally, the waveform of the applied alternating current may be arbitrary.

Next, as an example of a method of manufacturing an organic EL device, a method of manufacturing an organic EL device composed of an anode/hole injection layer/hole transport layer/host material and a light emitting layer/electron transport layer/electron injection layer/cathode made of a dopant material will be described. Explain.

<Deposition method>

After producing an anode by forming a thin film of an anode material by a vapor deposition method or the like on a suitable substrate, thin films of a hole injection layer and a hole transport layer are formed on this anode. A host material and a dopant material are co-deposited on this to form a thin film to form a light-emitting layer. An electron transport layer and an electron injection layer are formed on this light-emitting layer, and a thin film made of a cathode material is formed by a deposition method or the like to form a cathode, thereby forming the desired organic material. An EL device is obtained. In addition, when manufacturing the organic EL device described above, it is also possible to reverse the manufacturing order and fabricate the cathode, electron injection layer, electron transport layer, light emitting layer, hole transport layer, hole injection layer, and anode in that order.

<Wet film forming method>

The wet film forming method is performed by preparing a low-molecular-weight compound capable of forming each organic layer of an organic EL device as a liquid composition for forming an organic layer and using it. If there is no suitable organic solvent that dissolves the low-molecular compound, a composition for forming an organic layer can be prepared from a reactive compound obtained by substituting a reactive substituent on the low-molecular compound and polymerized with another monomer or main chain polymer having a soluble function. You may prepare.

The wet film forming method generally forms a coating film by going through an application process of applying a composition for forming an organic layer to a substrate and a drying process of removing a solvent from the applied composition for forming an organic layer. When the polymer compound has a crosslinkable substituent (this is also referred to as a crosslinkable polymer compound), it is further crosslinked through this drying process to form a crosslinked polymer. Depending on the difference in the application process, the method using a spin coater is the spin coat method, the method using the slit coater is the slit coat method, and the method using the plate is the gravure offset, reverse offset, flexo printing method, and inkjet printer. The method of doing this is called the inkjet method, and the method of emitting it in the form of a mist is called the spray method. The drying process includes methods such as air drying, heating, and reduced pressure drying. The drying process may be performed only once, or may be performed multiple times using different methods or conditions. Additionally, other methods may be used together, for example, baking under reduced pressure.

A wet film formation method is a film formation method using a solution, for example, some printing methods (inkjet methods), spin coating methods, cast methods, coating methods, etc. Unlike the vacuum deposition method, the wet film deposition method does not require the use of expensive vacuum deposition equipment and can be formed under atmospheric pressure. Additionally, the wet film forming method enables large-area and continuous production, leading to a reduction in manufacturing costs.

On the other hand, compared to the vacuum deposition method, the wet film forming method may be difficult to laminate. When producing a laminated film using a wet film forming method, it is necessary to prevent dissolution of the lower layer by the composition of the upper layer, so a composition with controlled solubility, crosslinking of the lower layer, and an orthogonal solvent (solvent that does not dissolve in each other), etc. This is used. However, even if these technologies are used, it is sometimes difficult to use the wet film forming method for application of all films.

Therefore, generally, a method of manufacturing an organic EL device using a wet film deposition method for only a few layers and a vacuum deposition method for the remaining layers is adopted.

For example, the procedure for manufacturing an organic EL device by partially applying a wet film forming method is shown below.

(Procedure 1) Film formation by vacuum deposition of anode

(Procedure 2) Film formation of a composition for forming a hole injection layer containing a hole injection layer material by a wet film forming method

(Procedure 3) Film formation of a composition for forming a hole transport layer containing a hole transport layer material by a wet film forming method

(Procedure 4) Film formation of a composition for forming an emitting layer containing a host material and a dopant material by a wet film forming method

(Procedure 5) Film formation of electron transport layer by vacuum deposition method

(Procedure 6) Film formation of electron injection layer by vacuum deposition method

(Procedure 7) Film formation by vacuum deposition of cathode

By going through this procedure, an organic EL device is obtained which consists of an anode/hole injection layer/hole transport layer/light emitting layer/electron transport layer/electron injection layer/cathode made of a host material and a dopant material.

Of course, the electron transport layer and the electron injection layer may also be formed by a wet film forming method using a layer forming composition containing the electron transport layer material and the electron injection layer material, respectively. At this time, it is preferable to use a means to prevent dissolution of the lower light emitting layer, or a means to form a film from the cathode side in the reverse order of the above.

<Other tabernacle methods>

Laser thermal imaging (LITI) can be used to form a film of the composition for forming an organic layer. LITI is a method of heating and depositing a compound attached to a substrate with a laser, and a composition for forming an organic layer can be used as the material applied to the substrate.

<Random process>

Appropriate treatment processes, cleaning processes, and drying processes may be appropriately added before and after each process of film formation. Examples of the treatment process include exposure treatment, plasma surface treatment, ultrasonic treatment, ozone treatment, washing treatment using an appropriate solvent, and heat treatment. Additionally, a series of processes for manufacturing a bank can also be mentioned.

Photolithography technology can be used to produce banks. As bank materials that can be used for photolithography, positive resist materials and negative resist materials can be used. Additionally, patternable printing methods such as inkjet printing, gravure offset printing, reverse offset printing, and screen printing can also be used. In this case, a permanent resist material may be used.

Materials used in the bank include polysaccharides and their derivatives, homopolymers and copolymers of hydroxyl-containing ethylenic monomers, biopolymer compounds, polyacryloyl compounds, polyester, polystyrene, polyimide, polyamidoimide, and polyether. Mead, polysulfide, polysulfone, polyphenylene, polyphenyl ether, polyurethane, epoxy (meth)acrylate, melamine (meth)acrylate, polyolefin, cyclic polyolefin, acrylonitrile-butadiene-styrene copolymer (ABS) ), silicone resin, polyvinyl chloride, chlorinated polyethylene, chlorinated polypropylene, polyacetate, polynorbonane (bicyclo [2.2.1]heptane), synthetic rubber, polyfluorobinylidene, polytetrafluoroethylene, polyhexamethylene Examples include, but are not limited to, fluorinated polymers such as fluoropropylene, copolymers of fluoroolefin-hydrocarbonolefin, and fluorocarbon polymers.

<Composition for forming organic layer used in wet film forming method>

The composition for forming an organic layer is obtained by dissolving a low-molecular compound capable of forming each organic layer of an organic EL device, or a high-molecular compound obtained by polymerizing the low-molecular compound, in an organic solvent. For example, the composition for forming a light-emitting layer includes at least one polycyclic aromatic compound (or a polymer compound thereof) as a dopant material as a first component, at least one host material as a second component, and at least one host material as a third component. Contains a variety of organic solvents. The first component functions as a dopant component of the light-emitting layer obtained from the composition, and the second component functions as a host component of the light-emitting layer. The third component functions as a solvent that dissolves the first and second components in the composition, and upon application, imparts a smooth and uniform surface shape by the controlled evaporation rate of the third component itself.

<Organic solvent>

The composition for forming an organic layer includes at least one organic solvent. By controlling the evaporation rate of the organic solvent during film formation, film formability, presence of defects, surface roughness, and smoothness of the coating film can be controlled and improved. Additionally, when forming a film using the inkjet method, the meniscus stability in the pinhole of the inkjet head can be controlled to control and improve ejection properties. Additionally, by controlling the drying rate of the film and the orientation of the derivative molecules, the electrical properties, luminescence properties, efficiency, and lifespan of an organic EL device having an organic layer obtained from the composition for forming the organic layer can be improved.

(1) Physical properties of organic solvents

The boiling point of at least one organic solvent is 130°C to 300°C, more preferably 140°C to 270°C, and even more preferably 150°C to 250°C. When the boiling point is higher than 130°C, it is preferable from the viewpoint of inkjet ejection properties. Additionally, a boiling point lower than 300°C is preferable from the viewpoint of defects in the coating film, surface roughness, residual solvent, and smoothness. The organic solvent more preferably contains two or more types of organic solvents from the viewpoints of good inkjet discharge properties, film forming properties, smoothness, and low residual solvent. On the other hand, in some cases, considering transportability, etc., the composition may be made into a solid state by removing the solvent from the composition for forming the organic layer.

Furthermore, the organic solvent includes a good solvent (GS) and a poor solvent (PS) for at least one type of solute, and the boiling point (BP _GS ) of the good solvent (GS) is the boiling point (BP PS ) of the poor solvent ( _PS ). A lower configuration is particularly preferred.

By adding a poor solvent with a high boiling point, the good solvent with a low boiling point volatilizes first during film formation, and the concentration of the contents in the composition and the concentration of the poor solvent increase, thereby promoting rapid film formation. As a result, a coating film with few defects, small surface roughness, and high smoothness is obtained.

The difference in solubility (S _GS -S _PS ) is preferably 1% or more, more preferably 3% or more, and even more preferably 5% or more. The difference in boiling points (BP _PS -BP _GS ) is preferably 10°C or higher, more preferably 30°C or higher, and even more preferably 50°C or higher.

After film formation, the organic solvent is removed from the coating film through a drying process such as vacuum, reduced pressure, or heating. When heating is performed, from the viewpoint of improving application film forming properties, it is preferably performed at a temperature below the glass transition temperature (Tg) of at least one type of solute + 30°C. Additionally, from the viewpoint of reducing residual solvent, it is preferable to heat at least 30°C or higher than the glass transition point (Tg) of at least one type of solute. Even if the heating temperature is lower than the boiling point of the organic solvent, the organic solvent is sufficiently removed because the film is thin. Additionally, drying may be performed multiple times at different temperatures, or multiple drying methods may be used in combination.

(2) Specific examples of organic solvents

Organic solvents used in the composition for forming an organic layer include alkylbenzene-based solvents, phenyl ether-based solvents, alkyl ether-based solvents, cyclic ketone-based solvents, aliphatic ketone-based solvents, monocyclic ketone-based solvents, and solvents having a diester skeleton. Fluorine-based solvents and the like can be mentioned, and specific examples include pentanol, hexanol, heptanol, octanol, nonanol, decanol, undecanol, dodecanol, tetradecanol, hexan-2-ol, and heptan-2-. ol, octan-2-ol, decane-2-ol, dodecane-2-ol, cyclohexanol, α-terpineol, β-terpineol, γ-terpineol, δ-terpineol, terpineol Pineol (mixture), ethylene glycol monomethyl ether acetate, propylene glycol monomethyl ether acetate, diethylene glycol dimethyl ether, dipropylene glycol dimethyl ether, diethylene glycol ethyl methyl ether, diethylene glycol isopropyl methyl ether, dipropylene glycol Monomethyl ether, diethylene glycol diethyl ether, diethylene glycol monomethyl ether, diethylene glycol butyl methyl ether, tripropylene glycol dimethyl ether, triethylene glycol dimethyl ether, diethylene glycol monobutyl ether, ethylene glycol monophenyl ether, Triethylene glycol monomethyl ether, diethylene glycol dibutyl ether, triethylene glycol butyl methyl ether, polyethylene glycol dimethyl ether, tetraethylene glycol dimethyl ether, p-xylene, m-xylene, o-xylene, 2,6-lutidine , 2-fluoro-m-xylene, 3-fluoro-o-xylene, 2-chlorobenzotrifluoride, cumene, toluene, 2-chloro-6-fluorotoluene, 2-fluoroanisole, anisole, 2,3-dimethylpyrazine, bromobenzene, 4-fluoroanisole, 3-fluoroanisole, 3-trifluoromethylanisole, mesitylene, 1,2,4-trimethylbenzene, t-butylbenzene , 2-methylanisole, phenetol, benzodioxole, 4-methylanisole, s-butylbenzene, 3-methylanisole, 4-fluoro-3-methylanisole, cymene, 1,2,3- Trimethylbenzene, 1,2-dichlorobenzene, 2-fluorobenzonitrile, 4-fluoroberatrol, 2,6-dimethylanisole, n-butylbenzene, 3-fluorobenzonitrile, decalin (decahydronaphthalene) , neopentylbenzene, 2,5-dimethylanisole, 2,4-dimethylanisole, benzonitrile, 3,5-dimethylanisole, diphenyl ether, 1-fluoro-3,5-dimethoxybenzene, benzoic acid. Methyl, isopentylbenzene, 3,4-dimethylanisole, o-tolnitrile, n-amylbenzene, veratrol, 1,2,3,4-tetrahydronaphthalene, ethyl benzoate, n-hexylbenzene, propyl benzoate, Cyclohexylbenzene, 1-methylnaphthalene, butyl benzoate, 2-methylbiphenyl, 3-phenoxytoluene, 2,2'-vitolyl, dodecylbenzene, dipentylbenzene, tetramethylbenzene, trimethoxybenzene, trimethylbenzene Methoxytoluene, 2,3-dihydrobenzofuran, 1-methyl-4-(propoxymethyl)benzene, 1-methyl-4-(butyloxymethyl)benzene, 1-methyl-4-(pentyloxymethyl) Benzene, 1-methyl-4-(hexyloxymethyl)benzene, 1-methyl-4-(heptyloxymethyl)benzene, benzylbutyl ether, benzylpentyl ether, benzylhexyl ether, benzylheptyl ether, benzyl octyl ether, etc. It can be done, but it is not limited to that. In addition, solvents may be used singly or mixed.

<Arbitrary ingredients>

The composition for forming an organic layer may contain arbitrary components as long as its properties are not impaired. Optional components include binders and surfactants.

(1) Binder

The composition for forming an organic layer may contain a binder. The binder forms a film during film formation and bonds the obtained film to the substrate. In addition, it serves to dissolve, disperse, and bind other components in the composition for forming the organic layer.

The binder used in the composition for forming the organic layer includes, for example, acrylic resin, polyethylene terephthalate, ethylene-vinyl acetate copolymer, ethylene-vinyl alcohol copolymer, acrylonitrile-ethylene-styrene copolymer (AES) resin, Ionomer, chlorinated polyether, diallyl phthalate resin, unsaturated polyester resin, polyethylene, polypropylene, polyvinyl chloride, polyvinylidene chloride, polystyrene, polyvinyl acetate, Teflon, acrylonitrile-butadiene-styrene copolymer (ABS) Resins, acrylonitrile-styrene copolymer (AS) resins, phenol resins, epoxy resins, melamine resins, urea resins, alkyd resins, polyurethanes, and copolymers of these resins and polymers, but are not limited thereto. No.

The binder used in the composition for forming an organic layer may be one type or may be used in mixture of multiple types.

(2)Surfactant

The composition for forming an organic layer may contain a surfactant, for example, to control the uniformity of the film surface, the solvent-philicity, and the liquid repellency of the film surface of the composition for forming the organic layer. Surfactants are classified into ionic and nonionic based on the structure of the hydrophilic group, and further classified into alkyl-based, silicone-based, and fluorine-based based on the structure of the hydrophobic group. In addition, from the molecular structure, it is classified into a single molecule system with a relatively small molecular weight and a simple structure, and a polymer system with a large molecular weight and side chains or branches. Additionally, based on composition, it is classified into a single system and a mixed system in which two or more types of surfactants and a base material are mixed. As a surfactant that can be used in the composition for forming the organic layer, all types of surfactants can be used.

As surfactants, for example, Polyflow No. 45, Polyflow KL-245, Polyflow No. 75, Polyflow No. 90, Polyflow No. 95 (brand name, manufactured by Kyoeisha Chemical Industry Co., Ltd.) , Disperbake 161, Disperbake 162, Disperbake 163, Disperbake 164, Disperbake 166, Disperbake 170, Disperbake 180, Disperbake 181, Disperbake 182, BYK300 , BYK306, BYK310, BYK320, BYK330, BYK342, BYK344, BYK346 (product name, Big Chemi Japan Co., Ltd.), KP-341, KP-358, KP-368, KF-96-50CS, KF-50-100CS (Product name, manufactured by Shin-Etsu Chemical Co., Ltd.), Suplon SC-101, Suplon KH-40 (Brand name, manufactured by Semi Chemical Co., Ltd.), Ptagent 222F, Ptagent 251, FTX-218 (Product name, ( (made by Neos Co., Ltd.), EFTOP EF-351, EFTOP EF-352, EFTOP EF-601, EFTOP EF-801, EFTOP EF-802 (brand name, made by Mitsubishi Materials Co., Ltd.), Megapak F-470, Megapak F-471, Megapak F-475, Megapak R-08, Megapak F-477, Megapak F-479, Megapak F-553, Megapak F-554 (brand name, manufactured by DIC Co., Ltd.), Fluo Roalkyl benzene sulfonate, fluoroalkyl carboxylate, fluoroalkyl polyoxyethylene ether, fluoroalkyl ammonium iodide, fluoroalkyl betaine, fluoroalkyl sulfonate, diglycerin tetrakis (fluoroalkyl poly oxyethylene ether), fluoroalkyl trimethyl ammonium salt, fluoroalkyl amino sulfonate, polyoxyethylene nonylphenyl ether, polyoxyethylene octylphenyl ether, polyoxyethylene alkyl ether, polyoxyethylene laurate, polyoxyethylene oleate, Polyoxyethylene stearate, polyoxyethylene laurylamine, sorbitan laurate, sorbitan palmitate, sorbitan stearate, sorbitan oleate, sorbitan fatty acid ester, polyoxyethylene sorbitan laurate, polyoxyethylene sorbitan Examples include bitan palmitate, polyoxyethylene sorbitan stearate, polyoxyethylene sorbitan oleate, polyoxyethylene naphthyl ether, alkylbenzene sulfonate, and alkyl diphenyl ether disulfonate.

In addition, surfactants may be used alone or two or more types may be used in combination.

<Composition and physical properties of composition for forming organic layer>

The content of each component in the composition for forming an organic layer is determined by the good solubility, storage stability, and film forming properties of each component in the composition for forming an organic layer, the high quality of the coating film obtained from the composition for forming an organic layer, and the inkjet method. It is determined taking into consideration the viewpoints of good discharge properties when used, good electrical characteristics, luminescence characteristics, efficiency, and lifespan of an organic EL device having an organic layer produced using the composition. For example, in the case of a composition for forming a light-emitting layer, the first component is 0.0001% to 2.0% by mass with respect to the total mass of the composition for forming a light-emitting layer, and the second component is 0.0999% by mass with respect to the total mass of the composition for forming a light-emitting layer. % to 8.0% by mass, and the third component is preferably 90.0% to 99.9% by mass relative to the total mass of the composition for forming the light emitting layer.

More preferably, the first component is 0.005 mass% to 1.0 mass% with respect to the total mass of the composition for forming a light-emitting layer, and the second component is 0.095 mass% to 4.0 mass% with respect to the total mass of the composition for forming a light-emitting layer. The three components are 95.0% by mass to 99.9% by mass with respect to the total mass of the composition for forming a light emitting layer. Even more preferably, the first component is 0.05 mass% to 0.5 mass% with respect to the total mass of the composition for forming a light-emitting layer, and the second component is 0.25 mass% to 2.5 mass% with respect to the total mass of the composition for forming a light-emitting layer. The third component is 97.0% by mass to 99.7% by mass with respect to the total mass of the composition for forming a light emitting layer.

The composition for forming an organic layer can be produced by appropriately selecting and performing the above-mentioned components by stirring, mixing, heating, cooling, dissolving, dispersing, etc., by a known method. In addition, after preparation, filtration, degassing (also called degassing), ion exchange treatment, and inert gas substitution/encapsulation treatment may be selected and performed as appropriate.

As for the viscosity of the composition for forming an organic layer, a high viscosity provides good film forming properties and good ejection properties when using the inkjet method. On the other hand, it is easy to create a thin film with a low viscosity. From this, the viscosity of the composition for forming the organic layer is preferably 0.3 to 3 mPa·s at 25°C, and more preferably 1 to 3 mPa·s. In the present invention, the viscosity is a value measured using a cone-plate rotational viscometer (cone plate type).

As for the surface tension of the composition for forming an organic layer, the lower the surface tension, the better film forming properties and a defect-free coating film are obtained. On the other hand, the higher the value, the better inkjet ejection properties are obtained. From this, the composition for forming the organic layer preferably has a surface tension of 20 to 40 mN/m at 25°C, and more preferably 20 to 30 mN/m. In the present invention, surface tension is a value measured using the drop method.

<Crosslinkable polymer compound: compound represented by formula (XLP-1)>

Next, a case where the above-mentioned polymer compound has a crosslinkable substituent will be described. Such a crosslinkable polymer compound is, for example, a compound represented by the following formula (XLP-1).

In equation (XLP-1),

MU is each independently a divalent group expressed by removing any two hydrogen atoms from an aromatic compound, EC is each independently a monovalent group expressed by removing any one hydrogen atom from an aromatic compound, and 2 in MU Hydrogen is replaced with EC or MU, and k is an integer from 2 to 50000. However, the compound represented by the formula (XLP-1) has at least one crosslinkable substituent (XLS), and preferably the content of the monovalent or divalent aromatic compound having a crosslinkable substituent is 0.1 to 80 mass per molecule. %am.

More specifically,

MU is each independently arylene, heteroarylene, diarylenearylamino, diarylenearylboryl, oxaborine-diyl, azaborine-diyl,

EC is each independently hydrogen, aryl, heteroaryl, diarylamino, diheteroarylamino, arylheteroarylamino, or aryloxy,

At least one hydrogen in MU and EC may be further substituted with aryl, heteroaryl, diarylamino, alkyl, and cycloalkyl,

k is an integer from 2 to 50000.

It is preferable that k is an integer of 20 to 50,000, and it is more preferable that it is an integer of 100 to 50,000.

At least one hydrogen in MU and EC in formula (XLP-1) may be substituted with alkyl having 1 to 24 carbon atoms, cycloalkyl having 3 to 24 carbon atoms, halogen or deuterium, and further, in the alkyl Any -CH ₂ - may be substituted with -O- or -Si(CH ₃ ) ₂ -, and any -CH 2 - excluding -CH ₂ - directly linked to EC in formula (XLP-1) in the above alkyl -CH ₂ - may be substituted with arylene having 6 to 24 carbon atoms, and any hydrogen in the alkyl may be substituted with fluorine.

Examples of MU include a divalent group expressed by removing two arbitrary hydrogen atoms from any of the following compounds.

More specifically, a divalent group represented by any of the structures below can be mentioned. In these, the MU combines with another MU or EC in *.

In addition, as EC, for example, a monovalent group represented by any of the structures below can be mentioned. In these, EC combines with MU at *.

In the compound represented by the formula (XLP-1), from the viewpoint of solubility and coating film forming properties, it is preferable that 10 to 100% of the MU in the molecule (k) total number (k) has alkyl having 1 to 24 carbon atoms, and MU in the molecule It is more preferable that 30 to 100% of the total number (k) of MU has alkyl with 1 to 18 carbon atoms (branched chain alkyl with 3 to 18 carbon atoms), and 50 to 100% of MU in the total number (k) of the MU in the molecule is more preferred. It is more preferable to have an alkyl with 1 to 12 carbon atoms (branched chain alkyl with 3 to 12 carbon atoms). On the other hand, from the viewpoint of in-plane orientation and charge transport, it is preferable that 10 to 100% of the MUs in the molecule have alkyls of 7 to 24 carbon atoms, and 30 to 100% of the total number (k) of the MUs in the molecule are alkyl. It is more preferable that MU has an alkyl with 7 to 24 carbon atoms (branched chain alkyl with 7 to 24 carbon atoms).

The content of the monovalent or divalent aromatic compound having a crosslinkable substituent is preferably 0.5 to 50% by mass, and more preferably 1 to 20% by mass.

The crosslinkable substituent (XLS) is not particularly limited as long as it is a group capable of further crosslinking the above-mentioned polymer compound, but a substituent with the following structure is preferable. * in each structural formula indicates the binding position.

L is each independently a single bond, -O-, -S-, >C=O, -O-C(=O)-, alkylene with 1 to 12 carbon atoms, oxyalkylene with 1 to 12 carbon atoms, and 1 carbon atom It is a polyoxyalkylene of ~12. Among the above substituents, groups represented by formula (XLS-1), formula (XLS-2), formula (XLS-3), formula (XLS-9), formula (XLS-10), or formula (XLS-17) are preferable. And, the group represented by formula (XLS-1), formula (XLS-3), or formula (XLS-17) is more preferable.

Examples of divalent aromatic compounds having a crosslinkable substituent include compounds having the following partial structures. * in the structural formula below indicates a binding position.

<Method for producing polymer compounds and crosslinkable polymer compounds>

The method for producing a polymer compound and a crosslinkable polymer compound will be explained taking the compound represented by the above-mentioned formula (XLP-1) as an example. These compounds can be synthesized by appropriately combining known production methods.

Solvents used in the reaction include aromatic solvents, saturated/unsaturated hydrocarbon solvents, alcohol solvents, and ether-based solvents, for example, dimethoxyethane, 2-(2-methoxyethoxy)ethane, 2- (2-ethoxyethoxy)ethane, etc. can be mentioned.

Additionally, the reaction may be performed in a two-phase system. When reacting in a two-phase system, a phase transfer catalyst such as quaternary ammonium salt may be added as needed.

When producing a compound of formula (XLP-1), it may be produced in one step or may be produced in multiple steps. Additionally, it may be carried out by a batch polymerization method in which the reaction is started after putting all the raw materials into the reaction vessel, or by a drop polymerization method in which the raw materials are added dropwise to the reaction vessel, or by precipitation in which the product precipitates as the reaction progresses. It may be carried out by a polymerization method, or it can be synthesized by appropriately combining them. For example, when synthesizing a compound represented by formula (XLP-1) in one step, a monomer with a polymerizable group bonded to the monomer unit (MU) and a monomer with a polymerizable group bonded to the end cap unit (EC) are placed in a reaction vessel. The target product is obtained by performing a reaction under the applied conditions. In addition, when synthesizing the compound represented by formula (XLP-1) in multiple steps, the monomer with the polymerizable group bonded to the monomer unit (MU) is polymerized to the desired molecular weight, and then the monomer with the polymerizable group bonded to the end cap unit (EC) The target product is obtained by adding and reacting. By performing a reaction in multiple steps by adding a monomer to which a polymerizable group is bonded to different types of monomer units (MU), a polymer having a concentration gradient with respect to the structure of the monomer unit can be produced. Additionally, after preparing the precursor polymer, the target polymer can be obtained through a post-reaction.

Additionally, the primary structure of the polymer can be controlled by selecting the polymerizable group of the monomer unit (MU). For example, as shown in synthesis schemes 1 to 3, polymers with random primary structures (synthesis scheme 1), polymers with regular primary structures (synthesis schemes 2 and 3), etc. are synthesized. It is possible, and can be used in appropriate combination depending on the target. Furthermore, by using a monomer having three or more polymerizable groups, hyperbranched polymers and dendrimers can be synthesized.

Monomers that can be used in the present invention include Japanese Patent Application Laid-Open No. 2010-189630, International Publication No. 2012/086671, International Publication No. 2013/191088, International Publication No. 2002/045184, International Publication No. 2011/049241, International Publication No. 2013/146806, International Publication No. 2005/049546, International Publication No. 2015/145871, Japanese Patent Publication No. 2010-215886, Japanese Patent Publication No. 2008-106241, International Publication No. 2016/031639, Japan It can be synthesized according to the method described in Patent Publication No. 2011-174062.

In addition, regarding the specific polymer synthesis sequence, Japanese Patent Application Laid-Open No. 2012-036388, International Publication No. 2015/008851, Japanese Patent Application Publication No. 2012-36381, Japanese Patent Application Publication No. 2012-144722, International Publication No. 2015/194448 The methods described in International Publication No. 2013/146806, International Publication No. 2015/145871, International Publication No. 2016/031639, International Publication No. 2016/125560, and International Publication No. 2011/049241 may be referred to.

2-1-9. abandonment electric field light emitting element Application example

The present invention can also be applied to a display device provided with an organic EL element or a lighting device provided with an organic EL element.

A display device or lighting device including an organic EL element can be manufactured by known methods, such as connecting the organic EL element according to the present embodiment and a known driving device, and known methods such as direct current drive, pulse drive, and alternating current drive. It can be driven by appropriately using the driving method.

Examples of display devices include panel displays such as color flat panel displays, and flexible displays such as flexible color organic electroluminescence (EL) displays (for example, Japanese Patent Application Laid-Open No. 10-335066, See Japanese Patent Publication No. 2003-321546, Japanese Patent Publication No. 2004-281086, etc.). Additionally, examples of display methods include matrix and segment methods. Additionally, the matrix display and segment display may coexist in the same panel.

In a matrix, pixels for display are arranged two-dimensionally, such as in a grid or mosaic, and characters or images are displayed as a set of pixels. The shape and size of the pixel are determined depending on the purpose. For example, for image and text display on computers, monitors, and televisions, square pixels with a side of 300 ㎛ or less are usually used, and in the case of large displays such as display panels, pixels on the order of mm per side are used. I do it. In the case of monochrome display, pixels of the same color can be arranged, but in the case of color display, red, green, and blue pixels are displayed in a row. In this case, there are typically delta types and stripe types. The driving method of this matrix may be either a linear sequential driving method or an active matrix driving method. Line-sequential driving has the advantage of having a simple structure, but when considering operation characteristics, the active matrix method is sometimes superior, so it is necessary to use it separately depending on the application.

In the segment method (type), a pattern is formed to display predetermined information, and a defined area is emitted. Examples include time and temperature displays in digital clocks and thermometers, operating status displays in audio devices and electronic cookers, and panel displays in automobiles.

Examples of lighting devices include lighting devices such as indoor lighting, backlights of liquid crystal display devices, etc. (for example, Japanese Patent Application Laid-Open No. 2003-257621, Japanese Patent Application Laid-Open No. 2003-277741, Japanese Patents (See Public Notice No. 2004-119211, etc.). Backlights are mainly used to improve the visibility of display devices that do not emit light themselves, and are used in liquid crystal displays, clocks, audio devices, automobile panels, displays, and signs. In particular, considering that it is difficult to reduce the thickness of liquid crystal display devices, especially computer-use backlights where thinness is an issue, because the conventional method consists of a fluorescent lamp or a light guide plate, the backlight using the light emitting element according to the present embodiment is thin. It is characterized by being lightweight.

2-2. Other organic devices

The polycyclic aromatic compound according to the present invention can be used in the production of organic field effect transistors, organic thin film solar cells, etc. in addition to the organic electroluminescent devices described above.

An organic field effect transistor refers to a transistor that controls current by an electric field generated by voltage input, and has a gate electrode in addition to the source and drain electrodes. It is a transistor that generates an electric field when a voltage is applied to the gate electrode and can control the current by arbitrarily stopping the flow of electrons (or holes) flowing between the source and drain electrodes. Field effect transistors are easier to miniaturize than simple transistors (bipolar transistors), and are often used as elements constituting integrated circuits and the like.

The structure of an organic field effect transistor usually has a source electrode and a drain electrode provided in contact with an organic semiconductor active layer formed using the polycyclic aromatic compound according to the present invention, and an insulating layer (dielectric layer) in contact with the organic semiconductor active layer. It is sufficient as long as the gate electrode is installed. Examples of the device structure include the following structure.

(1) Substrate/gate electrode/insulator layer/source electrode/drain electrode/organic semiconductor active layer

(2) Substrate/gate electrode/insulator layer/organic semiconductor active layer/source electrode/drain electrode

(3) Substrate/organic semiconductor active layer/source electrode/drain electrode/insulator layer/gate electrode

(4) Substrate/source electrode/drain electrode/organic semiconductor active layer/insulator layer/gate electrode

The organic field effect transistor configured in this way can be applied as a pixel driving switching element of an active matrix driving liquid crystal display or an organic electroluminescence display.

Organic thin film solar cells have a structure in which an anode such as ITO, a hole transport layer, a photoelectric conversion layer, an electron transport layer, and a cathode are stacked on a transparent substrate such as glass. The photoelectric conversion layer has a p-type semiconductor layer on the anode side and an n-type semiconductor layer on the cathode side. The polycyclic aromatic compound according to the present invention can be used as a material for a hole transport layer, a p-type semiconductor layer, an n-type semiconductor layer, and an electron transport layer, depending on its physical properties. The polycyclic aromatic compound according to the present invention can function as a hole transport material or electron transport material in an organic thin film solar cell. The organic thin film solar cell may be appropriately provided with a hole blocking layer, an electron blocking layer, an electron injection layer, a hole injection layer, a smoothing layer, etc. in addition to the above. For an organic thin film solar cell, known materials used in organic thin film solar cells can be appropriately selected and used in combination.

3. Wavelength conversion materials

The polycyclic aromatic compound of the present invention can be used as a wavelength conversion material. Currently, the application of multi-color technology based on color conversion method to liquid crystal monitors, organic EL displays, lighting, etc. is being actively studied. Color conversion refers to converting light emission from a light emitting body into light of a longer wavelength, for example, converting ultraviolet light or blue light into green light or red light emission. By forming a wavelength conversion material with this color conversion function into a film and combining it with a blue light source, for example, it becomes possible to extract the three primary colors of blue, green, and red from the blue light source, that is, to extract white light. . By using a white light source that combines a blue light source and a wavelength conversion film with a color conversion function as a light source unit and combining it with a liquid crystal driving part and a color filter, it is possible to produce a full color display. In addition, if there is no liquid crystal driving part, it can be used as a white light source, for example, it can be applied as a white light source such as LED lighting. Additionally, by using a blue organic EL device as a light source and using it in combination with a wavelength conversion film that converts blue light into green light and red light, it becomes possible to produce a full-color organic EL display without using a metal mask. In addition, by using blue micro LED as a light source in combination with a wavelength conversion film that converts blue light into green light and red light, it becomes possible to produce a low-cost, full-color micro LED display.

The polycyclic aromatic compound of the present invention can be used as this wavelength conversion material. Using the wavelength conversion material containing the polycyclic aromatic compound of the present invention, light from a light source or light-emitting device that generates ultraviolet light or shorter wavelength blue light is transmitted to a display device (a display device or a liquid crystal display device using an organic EL device). It can be converted into blue or green light with high color purity suitable for use in. Adjustment of the converted color can be performed by appropriately selecting the substituent of the polycyclic aromatic compound of the present invention, the binder resin used in the composition for wavelength conversion described later, etc. The wavelength conversion material can be prepared as a composition for wavelength conversion containing the polycyclic aromatic compound of the present invention. Additionally, a wavelength conversion film may be formed using this composition for wavelength conversion.

The composition for wavelength conversion may contain a binder resin, other additives, and a solvent in addition to the polycyclic aromatic compound of the present invention. As the binder resin, for example, those described in paragraphs 0173 to 0176 of International Publication No. 2016/190283 can be used. As other additives, compounds described in paragraphs 0177 to 0181 of International Publication No. 2016/190283 can be used. As the solvent, reference may be made to the description of the solvent contained in the composition for forming the emitting layer.

The wavelength conversion film includes a wavelength conversion layer formed by curing the composition for wavelength conversion. As a method of producing a wavelength conversion layer from a composition for wavelength conversion, a known film forming method may be referred to. The wavelength conversion film may consist only of a wavelength conversion layer formed from a composition containing the polycyclic aromatic compound of the present invention, or another wavelength conversion layer (for example, a wavelength conversion layer that converts blue light into green light or red light, It may also contain a wavelength conversion layer that converts to red light. The wavelength conversion film may further include a barrier layer to prevent the base layer or the color conversion layer from being deteriorated by oxygen, moisture, or heat.

[Example]

Hereinafter, the present invention will be described in more detail through examples, but the present invention is not limited to these.

<<Synthesis example>>

Synthesis Example (1): Synthesis of Compound (1-1) and Compound (2-1)

To a flask containing compound (I-1) (1.09 g) and tert-butylbenzene (7.0 ml), 1.6 M tert-butyllithium pentane solution (1.6 ml) was added at -30°C under a nitrogen atmosphere. After the dropwise addition was completed, the temperature was raised to 60°C and stirred for 2 hours, and components with a lower boiling point than tert-butylbenzene were removed by distillation under reduced pressure. It was cooled to -30°C, boron tribromide (0.63 g) was added, the temperature was raised to room temperature, and the mixture was stirred for 0.5 hours. After that, the mixture was cooled to 0°C again, N,N-diisopropylethylamine (0.43 ml) was added, and the mixture was stirred at room temperature until the heat generation subsided, then the temperature was raised to 120°C and heated and stirred for 3 hours. The reaction solution was cooled to room temperature, and an aqueous solution of sodium acetate cooled in an ice bath, followed by heptane, was added to separate the layers. Next, after purification by silica gel short pass column (eluent: toluene), the solvent was distilled off under reduced pressure, the obtained solid was dissolved in toluene, heptane was added, and heptane was reprecipitated, resulting in compound (I-2) (0.35 g). got it

A solution containing compound (I-2) (78.1 mg, 0.075 mmol), boron triiodide (470.3 mg, 1.20 mmol), 2,6-di-tert-butylpyridine (102 μL, 0.45 mmol), and toluene (2.0 ml). Lenk was stirred at 60°C for 4 hours. Afterwards, phosphate buffer solution (pH=6.8, 10 ml) was added to the reaction mixture at 0°C, the aqueous layer was separated, and extracted with toluene (20 ml, 3 times). Thereafter, the obtained crude product was subjected to silica gel chromatography (developing solvent: hexane/dichloromethane = 4/1, 3/1, 3/2, ethyl acetate) to separate the products, and each solvent was distilled off under reduced pressure, followed by hexane. By washing with (10 ml), compound (2-1) (2.9 mg) was obtained as a yellow solid. At the same time, compound (1-1) (3.4 mg) was obtained as a red solid.

The structure of compound (2-1) obtained was confirmed by NMR measurement.

¹ H-NMR (500MHz, CDCl ₃ ): δ=2.41(s, 6H), 2.58(s, 6H), 2.73(s, 6H), 2.86(s, 6H), 6.29(d, 2H), 6.71( d, 2H), 7.13(d, 2H), 7.22(d, 4H), 7.32(d, 4H), 7.47 (t, 2H), 7.53(d, 2H), 7.78(s, 1H), 8.21(s , 2H), 8.30(s, 2H), 8.48(s, 2H), 8.69(s, 2H), 8.83(s, 2H).

The structure of compound (1-1) obtained was confirmed by NMR measurement.

¹ H-NMR (500MHz, CDCl ₃ ): δ=2.41(s, 6H), 2.58(s, 6H), 2.73(s, 6H), 2.86(s, 6H), 6.29(d, 2H), 6.71( d, 2H), 7.13(d, 2H), 7.22(d, 4H), 7.32(d, 4H), 7.47 (t, 2H), 7.53(d, 2H), 7.78(s, 1H), 8.21(s , 2H), 8.30(s, 2H), 8.48(s, 2H), 8.69(s, 2H), 8.83(s, 2H).

By appropriately changing the raw material compounds, other compounds of the present invention can be synthesized by a method similar to the above-described synthesis example.

<<Evaluation of absorption characteristics and luminescence characteristics>>

The absorption spectrum of the sample was measured using an ultraviolet-visible-near-infrared spectrophotometer (UV-2600, Shimadzu Corporation). In addition, the fluorescence spectrum or phosphorescence spectrum of the sample was measured using a spectrofluorometer (Hitachi Hi-Tech Co., Ltd., F-7000).

Regarding the measurement of the fluorescence spectrum, photoluminescence was measured by excitation with an appropriate excitation wavelength at room temperature. The measurement of the phosphorescence spectrum was performed while the sample was immersed in liquid nitrogen (temperature 77K) using the included cooling unit. In order to observe the phosphorescence spectrum, the delay time from excitation light irradiation to the start of measurement was adjusted using an optical chopper. The sample was excited with an appropriate excitation wavelength and photoluminescence was measured.

Additionally, the fluorescence quantum yield (PLQY) was measured using an absolute PL quantum yield measuring device (C9920-02G, manufactured by Hamamatsu Photonics Co., Ltd.).

Evaluation of fluorescence lifetime (delayed fluorescence)

The fluorescence lifetime was measured at 300K using a fluorescence lifetime measuring device (C11367-01, manufactured by Hamamatsu Photonics Co., Ltd.). Specifically, the emission component with fast fluorescence lifetime and the emission component with slow fluorescence lifetime were observed at the maximum emission wavelength measured by an appropriate excitation wavelength. In measuring the fluorescence lifetime of general organic EL materials that emit fluorescence at room temperature, a slow emission component involving a triplet component derived from phosphorescence is rarely observed due to deactivation of the triplet component by heat. When a slow luminescence component is observed in the compound being evaluated, the triplet energy with a long excitation life moves to the singlet energy due to thermal activity, resulting in observation as delayed fluorescence.

Calculation of energy gap (Eg)

Eg = 1240/A was calculated from A (nm) at the long-wavelength end of the absorption spectrum obtained by the above-described method.

E( S,Sh ), E( T,Sh ) and of ΔE(ST) Calculation

The lowest singlet excitation energy level E(S,Sh) is obtained from the wavelength BSh(nm) at the intersection of the baseline and the tangent passing through the peak short-wavelength side inflection point of the fluorescence spectrum, E(S,Sh)=1240/ Calculated by BSh. Additionally, the lowest triplet excitation energy level E(T,Sh) is obtained from the wavelength CSh(nm) at the intersection of the baseline and the tangent passing through the inflection point on the peak short wavelength side of the phosphorescence spectrum, E(T,Sh) Calculated by =1240/CSh.

ΔE(ST) is defined by ΔE(ST)=E(S,Sh)-E(T,Sh), which is the energy difference between E(S,Sh) and E(T,Sh). In addition, ΔE(ST) is, for example, “Purely organic electroluminescent material realizing 100% conversion from electricity to light”, H.Kaji, H.Suzuki, T.Fukushima, K.Shizu, K.Katsuaki, S.Kubo , T.Komino, H.Oiwa, F.Suzuki, A.Wakamiya, Y.Murata, C.Adachi, Nat.Commun.2015, 6, 8476.

<Example A1>

Evaluation of basic properties of compound (1-1)

A solution was prepared by dissolving compound (1-1) in toluene at a concentration of 1E-5M, and the absorption and luminescence characteristics were measured. The solution was bubbled with nitrogen to remove dissolved oxygen, and then PLQY and fluorescence lifetime were measured.

<Example A2, Comparative Example A1>

In the evaluation of Example A1, the evaluation was conducted under the same conditions except that compound (1-1) was changed to compound (2-1), new-DABNA. The results are summarized in Table 1.

<<Manufacturing and evaluation of vapor-deposited organic EL devices>>

Next, the fabrication and evaluation of an organic EL device using the polycyclic aromatic compound of the present invention are described.

Evaluation items include driving voltage (V), emission wavelength (nm), CIE chromaticity (x, y), external quantum efficiency (%), maximum wavelength of emission spectrum (nm), and full width at half maximum (nm). For these evaluation items, appropriate values of light emission luminance can be used.

The quantum efficiency of a light-emitting device includes internal quantum efficiency and external quantum efficiency. The internal quantum efficiency represents the rate at which external energy injected as electrons (or holes) into the light-emitting layer of the light-emitting device is converted purely into photons. On the other hand, the external quantum efficiency is calculated based on the amount of photons emitted to the outside of the light-emitting device, but some of the photons generated in the light-emitting layer are absorbed or continuously reflected inside the light-emitting device, thereby causing the photons to be emitted to the outside of the light-emitting device. Because it is not emitted to the outside, the external quantum efficiency is lower than the internal quantum efficiency.

The measurement methods for spectral radiance (emission spectrum) and external quantum efficiency are as follows. The device was made to emit light by applying voltage using a voltage/current generator R6144 manufactured by Advantist. Using a spectral radiance meter SR-3AR manufactured by TOPCON, the spectral radiance in the visible region was measured from the direction perpendicular to the light emitting surface. Assuming that the light-emitting surface is a completely diffusing surface, the value of the measured spectral radiance of each wavelength component divided by the wavelength energy and multiplied by π is the number of photons at each wavelength. Next, the number of photons was integrated in the entire observed wavelength range, and was taken as the total number of photons emitted from the device. The value of the applied current divided by the basic charge is the number of carriers injected into the device, and the number of total photons emitted from the device divided by the number of carriers injected into the device is the external quantum efficiency. Additionally, the half width of the emission spectrum is calculated as the width between the upper and lower wavelengths at which the intensity is 50%, with the maximum emission wavelength as the center.

[Comparative Example 1-1]

A 26 mm x 28 mm x 0.7 mm glass substrate (manufactured by Opto Science Co., Ltd.) made by polishing ITO to a thickness of 200 nm by sputtering to 120 nm was used as a transparent support substrate. This transparent support substrate was fixed to the substrate holder of a commercially available vapor deposition device (manufactured by Showa Vacuum Co., Ltd.), and HAT-CN, HTL-1, TcTa, ETL-1, new-DABNA, and ET7 were added thereto, respectively. A wearing boat, a tungsten deposition boat containing LiF and aluminum, respectively, were installed.

Each of the following layers was formed sequentially on the ITO film of the transparent support substrate. The pressure of the vacuum chamber was reduced to 5X10 ^-4 Pa, and first, HAT-CN was heated and deposited to a film thickness of 5 nm to form a hole injection layer. Next, HTL-1 was heated and deposited to a film thickness of 90 nm to form hole transport layer 1, and TcTa was further heated and deposited to a film thickness of 10 nm to form hole transport layer 2. Next, ETL-1 and new-DABNA were simultaneously heated and deposited to a film thickness of 20 nm to form a light-emitting layer. The deposition rate was adjusted so that the mass ratio of ETL-1 and new-DABNA was about 99:1. Next, ETL-1 was heated and deposited to a film thickness of 20 nm to form electron transport layer 1, and ET7 was further heated and deposited to a film thickness of 10 nm to form electron transport layer 2. The deposition rate of each layer was 0.01 to 1 nm/sec. After that, LiF was heated and deposited at a deposition rate of 0.01 to 0.1 nm/sec to a film thickness of 1 nm, and then aluminum was heated and deposited to a film thickness of 100 nm to form a cathode, thereby obtaining an organic EL device. At this time, the deposition rate of aluminum was adjusted to be 1 to 10 nm/sec.

[Example 1-1 and Example 1-2]

Organic EL devices of Examples 1-1 and 1-2 were obtained in the same manner as in Comparative Example 1-1, except that new-DABNA in Comparative Example 1-1 was changed to the compounds shown in Table 2.

[Examples 2-1 to 2, Examples 3-1 to 2, Examples 4-1 to 2, Comparative Example 2-1, Comparative Example 3-1, and Comparative Example 4-1]

ETL-1 (host) of Comparative Example 1-1 was added to TcTa and ETL-1 (host 1 and host 2) shown in Table 3, and new-DABNA was added to the emitting dopant or assisting dopant and imitating dopant shown in Table 3. Examples 2-1 to 2, Examples 3-1 to 2, Examples 4-1 to 2, Comparative Examples 2-1, and Comparative Example 3 in the same order as Comparative Example 1-1 except for changing to a dopant. -1, and the organic EL device of Comparative Example 4-1 were obtained.

Meanwhile, in Table 3, “Host 1” corresponds to a hole-transporting host material, and “Host 2” corresponds to an electron-transporting host material.

The chemical structures of the compounds used in the production of each of the above devices are shown below.

Examples 1-1 to 2, Examples 2-1 to 2, Examples 3-1 to 2, Examples 4-1 to 2, Comparative Example 1-1, Comparative Example 2-1, Comparative Example 3-1 and For the organic EL device of Comparative Example 4-1, a direct current voltage was applied using the ITO electrode as the anode and the LiF/aluminum electrode as the cathode, and the maximum emission wavelength (EL) and external quantum efficiency at a luminance of 1000 cd/m ² (EQE) and LT50 (the time until the initial luminance reaches 500 cd/m ² when continuously driven at a current density of 1000 cd/m ² ) were measured.

Table 4 shows the evaluation results of each device.

From comparison with the comparative example, it can be seen that green and highly efficient light emission is obtained in an organic EL device using a polycyclic aromatic compound having a structure expressed by formula (1) or formula (2), and at the same time, it has a long lifespan.

<<Fabrication and evaluation of coated organic EL devices>>

Next, an organic EL device obtained by applying and forming an organic layer will be described.

<Synthesis of polymer host compound: SPH-101>

SPH-101 was synthesized according to the method described in International Publication No. 2015/008851. A copolymer in which M2 or M3 is bonded next to M1 is obtained, and from the injection ratio, each unit is estimated to be 50:26:24 (molar ratio). In the structural formula below, Bpin is pinacolat boryl, and * is the connection position of each unit.

<Synthesis of polymer hole transport compound: XLP-101>

XLP-101 was synthesized according to the method described in Japanese Patent Application Laid-Open No. 2018-61028. A copolymer in which M5 or M6 is bonded next to M4 is obtained, and from the injection ratio, each unit is estimated to be 40:10:50 (molar ratio). Bpin is pinacolatboril, and * is the connection position of each unit.

<Example 5-1 to Example 5-9>

A coating solution for the materials forming each layer is prepared to produce a coating-type organic EL device.

<Production of organic EL devices of Examples 5-1 to 5-3>

Table 5 shows the material composition of each layer in the organic EL device.

The structure of “ET1” in Table 5 is shown below.

<Preparation of composition (1) for forming light-emitting layer>

The composition (1) for forming a light-emitting layer is prepared by stirring the following ingredients until a uniform solution is formed. By spin-coating the prepared composition for forming a light-emitting layer on a glass substrate and heating and drying it under reduced pressure, a coating film with no film defects and excellent smoothness is obtained.

Compound (A) 0.04% by mass

SPH-101 1.96% by mass

Xylene 69.00% by mass

Decalin 29.00% by mass

On the other hand, compound (A) is a polycyclic aromatic compound (e.g., compound (1-1)) having a structure containing a structural unit represented by formula (1) or formula (2), and the polycyclic aromatic compound is used as a monomer (That is, the monomer has a reactive substituent), which is a polymer compound polymerized or a polymer crosslinked product obtained by further crosslinking the polymer compound. The polymer compound for obtaining a cross-linked polymer has a cross-linkable substituent.

<PEDOT: PSS solution>

A commercially available PEDOT:PSS solution (Clevios(TM) P VP AI4083, water dispersion of PEDOT:PSS, manufactured by Heraeus Holdings) was used.

<Preparation of OTPD solution>

OTPD (LT-N159, manufactured by Luminescence Technology Corp.) and IK-2 (photocation polymerization initiator, manufactured by San Apro Corporation) were dissolved in toluene to prepare an OTPD solution with an OTPD concentration of 0.7% by mass and an IK-2 concentration of 0.007% by mass. do.

<Preparation of XLP-101 solution>

XLP-101 was dissolved in xylene at a concentration of 0.6 mass% to prepare a 0.6 mass% XLP-101 solution.

<Preparation of PCz solution>

PCz (polyvinylcarbazole) is dissolved in dichlorobenzene to prepare a 0.7% by mass PCz solution.

<Example 5-1>

A PEDOT:PSS solution is spin-coated on a glass substrate on which ITO has been deposited to a thickness of 150 nm, and baked on a hot plate at 200°C for 1 hour to form a PEDOT:PSS film with a film thickness of 40 nm (hole injection layer). Next, the OTPD solution is spin-coated, dried on a hot plate at 80°C for 10 minutes, exposed with an exposure machine at an exposure intensity of 100 mJ/cm ² , and baked on a hot plate at 100°C for 1 hour to form a film insoluble in the solution. An OTPD film with a thickness of 30 nm is formed (hole transport layer). Next, the composition for forming a light-emitting layer (1) is spin-coated and baked on a hot plate at 120°C for 1 hour to form a light-emitting layer with a film thickness of 20 nm.

The produced multilayer film was fixed to the substrate holder of a commercially available vapor deposition device (manufactured by Showa Vacuum Co., Ltd.), and a molybdenum deposition boat containing ET1, a molybdenum deposition boat containing LiF, and a tungsten deposition boat containing aluminum were used. Install. After reducing the pressure of the vacuum bath to 5Х10 ^-4 Pa, ET1 is heated and deposited to a film thickness of 30 nm to form an electron transport layer. The deposition rate when forming the electron transport layer is 1 nm/sec. Afterwards, LiF is heated and deposited at a deposition rate of 0.01 to 0.1 nm/sec to achieve a film thickness of 1 nm. Next, aluminum is heated and deposited to a film thickness of 100 nm to form a cathode. In this way, an organic EL device is obtained.

<Example 5-2>

An organic EL device was obtained in the same manner as in Example 5-1. Meanwhile, for the hole transport layer, a film with a thickness of 30 nm is formed by spin-coating an XLP-101 solution and baking it on a hot plate at 200°C for 1 hour.

<Example 5-3>

An organic EL device was obtained in the same manner as in Example 5-1. Meanwhile, for the hole transport layer, a 30 nm thick film is formed by spin coating a PCz solution and baking it on a hot plate at 120°C for 1 hour.

<Evaluation of organic EL devices of Examples 5-1 to 5-3>

The application-type organic EL device obtained as described above can be expected to have excellent driving voltage and external quantum efficiency, similar to the deposition-type organic EL device.

<Production of organic EL devices of Examples 5-4 to 5-6>

Table 6 shows the material composition of each layer in the organic EL device.

<Preparation of compositions (2) to (4) for forming a light-emitting layer>

The composition (2) for forming a light-emitting layer is prepared by stirring the following ingredients until a uniform solution is formed.

Compound (A) 0.02% by mass

mCBP 1.98% by mass

Toluene 98.00% by mass

The composition (3) for forming a light-emitting layer is prepared by stirring the following ingredients until a uniform solution is formed.

Compound (A) 0.02% by mass

SPH-101 1.98% by mass

Xylene 98.00% by mass

The composition (4) for forming a light-emitting layer is prepared by stirring the following ingredients until a uniform solution is formed.

Compound (A) 0.02% by mass

DOBNA 1.98% by mass

Toluene 98.00% by mass

In Table 7, "mCBP" is 3,3'-bis(N-carbazolyl)-1,1'-biphenyl, and "DOBNA" is 3,11-di-o-tolyl-5,9- Dioxa-13b-boranaphtho[3,2,1-de]anthracene, and “TSPO1” is diphenyl[4-(triphenylsilyl)phenyl]phosphine oxide. The chemical structure is shown below.

<Example 5-4>

A solution of ND-3202 (manufactured by Nissan Chemical Industries) was spin-coated on a glass substrate on which ITO had been deposited to a thickness of 45 nm, and then heated at 50°C for 3 minutes in an air atmosphere and further heated at 230°C for 15 minutes to increase the film thickness. A 50 nm ND-3202 film is formed (hole injection layer). Next, the XLP-101 solution is spin-coated and heated on a hot plate at 200°C for 30 minutes in a nitrogen gas atmosphere to form an XLP-101 film with a film thickness of 20 nm (hole transport layer). Next, the composition for forming a light-emitting layer (2) is spin-coated and heated at 130°C for 10 minutes in a nitrogen gas atmosphere to form a 20 nm light-emitting layer.

The produced multilayer film was fixed to the substrate holder of a commercially available vapor deposition device (manufactured by Showa Vacuum Co., Ltd.), and a molybdenum deposition boat containing TSPO1, a molybdenum deposition boat containing LiF, and a tungsten deposition boat containing aluminum were used. Install. After reducing the pressure of the vacuum bath to 5Х10 ^-4 Pa, TSPO1 is heated and deposited to a film thickness of 30 nm to form an electron transport layer. The deposition rate when forming the electron transport layer is 1 nm/sec. Afterwards, LiF is heated and deposited at a deposition rate of 0.01 to 0.1 nm/sec to achieve a film thickness of 1 nm. Next, aluminum is heated and deposited to a film thickness of 100 nm to form a cathode. In this way, an organic EL device is obtained.

<Example 5-5 and Example 5-6>

An organic EL device was obtained in the same manner as in Example 5-4 using the composition (3) or (4) for forming the light emitting layer.

<Evaluation of organic EL devices of Examples 5-4 to 5-6>

The application-type organic EL device obtained as described above can be expected to have excellent driving voltage and external quantum efficiency, similar to the deposition-type organic EL device.

<Production of organic EL devices of Examples 5-7 to 5-9>

Table 7 shows the material composition of each layer in the organic EL device.

<Preparation of compositions (5) to (7) for forming a light-emitting layer>

The composition (5) for forming a light-emitting layer is prepared by stirring the following ingredients until a uniform solution is formed.

Compound (A) 0.02% by mass

2PXZ-TAZ 0.18% by mass

mCBP 1.80% by mass

Toluene 98.00% by mass

The composition (6) for forming a light-emitting layer is prepared by stirring the following components until a uniform solution is formed.

Compound (A) 0.02% by mass

2PXZ-TAZ 0.18% by mass

SPH-101 1.80% by mass

Xylene 98.00% by mass

The composition (7) for forming a light-emitting layer is prepared by stirring the following ingredients until a uniform solution is formed.

Compound (A) 0.02% by mass

2PXZ-TAZ 0.18% by mass

DOBNA 1.80% by mass

Toluene 98.00% by mass

In Table 7, “2PXZ-TAZ” is 10,10'-((4-phenyl-4H-1,2,4-triazole-3,5-diyl)bis(4,1-phenylene)) It is bis(10H-phenoxazine). The chemical structure is shown below.

<Example 5-7>

A solution of ND-3202 (manufactured by Nissan Chemical Industries) was spin-coated on a glass substrate on which ITO had been deposited to a thickness of 45 nm, and then heated at 50°C for 3 minutes in an air atmosphere and further heated at 230°C for 15 minutes to increase the film thickness. A 50 nm ND-3202 film is formed (hole injection layer). Next, the XLP-101 solution is spin-coated and heated on a hot plate at 200°C for 30 minutes in a nitrogen gas atmosphere to form an XLP-101 film with a film thickness of 20 nm (hole transport layer). Next, the composition 5 for forming a light-emitting layer is spin-coated and heated at 130°C for 10 minutes in a nitrogen gas atmosphere to form a 20 nm light-emitting layer.

The produced multilayer film was fixed to the substrate holder of a commercially available vapor deposition device (manufactured by Showa Vacuum Co., Ltd.), and a molybdenum deposition boat containing TSPO1, a molybdenum deposition boat containing LiF, and a tungsten deposition boat containing aluminum were used. Install. After reducing the pressure of the vacuum bath to 5Х10 ^-4 Pa, TSPO1 is heated and deposited to a film thickness of 30 nm to form an electron transport layer. The deposition rate when forming the electron transport layer is 1 nm/sec. Afterwards, LiF is heated and deposited at a deposition rate of 0.01 to 0.1 nm/sec to achieve a film thickness of 1 nm. Next, aluminum is heated and deposited to a film thickness of 100 nm to form a cathode. In this way, an organic EL device is obtained.

<Example 5-8 and Example 5-9>

An organic EL device was obtained in the same manner as in Example 5-7 using the composition (6) or (7) for forming the light emitting layer.

<Evaluation of organic EL devices of Examples 5-7 to 5-9>

The application-type organic EL device obtained as described above can be expected to have excellent driving voltage and external quantum efficiency, similar to the deposition-type organic EL device.

100 Organic electroluminescent device
101 substrate
102 anode
103 hole injection layer
104 hole transport layer
105 emitting layer
106 electron transport layer
107 electron injection layer
108 cathode

Claims (20)

Polycyclic aromatic compounds having a structure containing a structural unit represented by formula (1) or formula (2);

In equation (1),
Ring B, ring C, ring D, ring E, ring F, ring G, ring H, and ring I are each independently a substituted or unsubstituted aryl ring or a substituted or unsubstituted heteroaryl ring,
The broken line connecting the C ring and the D ring indicates that the C ring and the D ring are not bonded at the position of the dashed line, or are bonded through a single bond or linking group at the position of the broken line,
Z is -C(-R ^Z )= or -N=, R ^Z is hydrogen or a substituent,
X is ^each independently a single bond, > _NR ^NX , > ^O , >C ( _-R ^C It is substituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CX and R ^IX are each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted. It is substituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and two R ^CX may be bonded to each other to form a ring, and two R ^IX may be bonded to each other to form a ring. R ^NX , R ^CX and R ^IX may each be bonded to one or two rings to which X containing itself is bonded,
Y is each independently, >B-, >P-, >P(=O)-, >P(=S)-, >Al-, >Ga-, >As-, >C(-R ^Y )- , >Si(-R ^Y )-, or >Ge(-R ^Y )-, where R ^Y is each independently optionally substituted aryl, optionally substituted heteroaryl, optionally substituted alkyl, or substituted It is a cycloalkyl that may be
In the above structure, at least one selected from the group consisting of an aryl ring and a heteroaryl ring may be condensed with at least one cycloalkane, and the cycloalkane may be substituted with at least one substituent, and the cycloalkane may be At least one -CH ₂ - in may be substituted with -O-,
At least one hydrogen in the above structure may be substituted with cyano, halogen, or deuterium. According to paragraph 1,
When the B ring, C ring, D ring, E ring, F ring, G ring, H ring, and I ring are each a substituted aryl ring or a substituted heteroaryl ring, the substituents are represented by the substituent group Z and formula (A30). At least one substituent selected from the group consisting of substituents,
Substituent group Z is,
Aryl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl, and cycloalkyl;
heteroaryl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl;
diarylamino which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl (two aryls may be bonded to each other through a linking group);
diheteroarylamino which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl (two heteroaryls may be bonded to each other through a linking group);
Arylheteroarylamino which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl (aryl and heteroaryl may be bonded to each other through a linking group);
diarylboryl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl (two aryls may be bonded through a single bond or linking group);
alkyl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, and cycloalkyl;
Cycloalkyl which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl and cycloalkyl;
alkoxy optionally substituted with at least one group selected from the group consisting of aryl, heteroaryl, and cycloalkyl;
aryloxy which may be substituted with at least one group selected from the group consisting of aryl, heteroaryl, alkyl, and cycloalkyl; and
Consists of substituted silyl,

In equation (A30),
Ak is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted cycloalkyl, or substituted or unsubstituted cycloalkenyl, and the alkyl, alkenyl, cycloalkyl and cycloalkenyl At least one -CH ₂ - may be substituted with -O- or -S-,
R ^Ak is substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^Ak may be bonded to Ak through a linking group or single bond. , * is the binding position,
Polycyclic aromatic compounds. The polycyclic aromatic compound according to claim 2, expressed by formula (1). The polycyclic aromatic compound according to claim 3, represented by the following formula (1-b);

In equation (1-b),
Z is each independently -C(-R ^Z )= or -N=,
R ^Z is each independently hydrogen or a substituent,
When R ^Z is a substituent, the substituent is any one selected from the substituent group Z or a substituent represented by the formula (A30),
Two adjacent ^R
Z=Z may each independently be >NR, >O, >C(-R) ₂ , >Si(-R) ₂ , >S, or >Se, wherein the >NR and the >C(-R) ₂ and R of >Si(-R) ₂ is each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, >C(-R) ₂ and the two R of >Si(-R) ₂ may be bonded to each other to form a ring,
X is each independently >NR ^NX , >O, >C(-R ^CX ) ₂ , >S, or >Se, and R ^NX is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, is substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^C It is a cycloalkyl, and two R ^CX may be bonded to each other to form a ring, and R ^NX and R ^CX are each bonded to one or two or more of the You can do it,
L is a single bond, >NR ^NL , >O, >C(-R ^CL ) ₂ , >S, or >Se, and R ^NL is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CL is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl. It is an alkyl, and two R ^CL may be bonded to each other to form a ring, and R ^NL and R ^CL are each bonded to one or two or more of Z bonded to the carbon atom to which L bonded, including itself, You can have it,
In the above structure, at least one aryl ring or heteroaryl ring may be condensed with at least one cycloalkane, the cycloalkane may be substituted with at least one substituent, and at least one substituent in the cycloalkane may be substituted. -CH ₂ - may be substituted with -O-,
At least one hydrogen in the above structure may be substituted with cyano, halogen, or deuterium. The polyaromatic compound of claim 4, wherein all Z's are -C(-R ^Z )= and X's are each independently >O, >NR ^NX , or >S. The method according to claim 4 or 5, wherein ^R , polycyclic aromatic compounds. According to claim 3, a polycyclic aromatic compound represented by the following formula;

where Me is methyl. The polycyclic aromatic compound according to claim 2, which is represented by formula (2). The polycyclic aromatic compound according to claim 8, represented by the following formula (2-b);

In equation (2-b),
Z is each independently -C(-R ^Z )= or -N=,
R ^Z is each independently hydrogen or a substituent,
When R ^Z is a substituent, the substituent is any one selected from the substituent group Z or a substituent represented by the formula (A30),
Two adjacent ^R
Z=Z may each independently be >NR, >O, >C(-R) ₂ , >Si(-R) ₂ , >S, or >Se, wherein the >NR and the >C(-R) ₂ and R of >Si(-R) ₂ is each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, >C(-R) ₂ and the two R of >Si(-R) ₂ may be bonded to each other to form a ring,
X is each independently >NR ^NX , >O, >C(-R ^CX ) ₂ , >S, or >Se, and R ^NX is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, is substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^C It is a cycloalkyl, and two R ^CX may be bonded to each other to form a ring, and R ^NX and R ^CX are each bonded to one or two or more of the You can do it,
L is a single bond, >NR ^NL , >O, >C(-R ^CL ) ₂ , >S, or >Se, and R ^NL is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CL is hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl. It is an alkyl, and two R ^CL may be bonded to each other to form a ring, and R ^NL and R ^CL are each bonded to one or two or more of Z bonded to the carbon atom to which L bonded, including itself, You can have it,
In the above structure, at least one aryl ring or heteroaryl ring may be condensed with at least one cycloalkane, the cycloalkane may be substituted with at least one substituent, and at least one substituent in the cycloalkane may be substituted. -CH ₂ - may be substituted with -O-,
At least one hydrogen in the above structure may be substituted with cyano, halogen, or deuterium. The polyaromatic compound of claim 9, wherein all Z's are -C(-R ^Z )= and X's are each independently >O, >NR ^NX , or >S. The method of claim 9 or 10, wherein R ^Z is each independently hydrogen, alkyl, phenyl optionally substituted by alkyl, diphenylamino optionally substituted by alkyl, or carbazolyl optionally substituted by alkyl. , polycyclic aromatic compounds. The polycyclic aromatic compound according to claim 8, represented by the following formula;

where Me is methyl. A polymer compound having a number average molecular weight of 2000 to 1.0×10 ⁸ , wherein the polycyclic aromatic compound according to any one of claims 1 to 12 is polymerized with a reactive compound substituted with a reactive substituent as a monomer. A material for an organic device containing the polycyclic aromatic compound according to any one of claims 1 to 12. The material for an organic device according to claim 14, wherein the material for an organic device is a material for an organic electroluminescent element, a material for an organic field effect transistor, a material for an organic thin film solar cell, or a material for a wavelength conversion filter. An organic electroluminescent element having a pair of electrodes consisting of an anode and a cathode and an organic layer disposed between the pair of electrodes, wherein the organic layer contains the polyaromatic compound according to any one of claims 1 to 12. The organic electroluminescent device according to claim 16, wherein the organic layer is a light-emitting layer. A display or lighting device comprising the organic electroluminescent element according to claim 16 or 17. A method for producing a polycyclic aromatic compound according to any one of claims 1 to 12, comprising:
By adding a boronating agent and a Bronsted base to the compound represented by the formula (Int) and reacting it, a mixture of the polycyclic aromatic compound represented by the formula (1) and the polycyclic aromatic compound represented by the formula (2) is obtained. Manufacturing method including;

In the expression (Int),
Ring B, ring C, ring D, ring E, ring F, ring G, ring H, and ring I are each independently a substituted or unsubstituted aryl ring or a substituted or unsubstituted heteroaryl ring,
The broken line connecting the C ring and the D ring indicates that the C ring and the D ring are not bonded at the position of the dashed line, or are bonded through a single bond or linking group at the position of the broken line,
Z is -C(-R ^Z )= or -N=, R ^Z is hydrogen or a substituent,
X is ^each independently a single bond, > _NR ^NX , > ^O , >C ( _-R ^C It is substituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CX and R ^IX are each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted. It is substituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and two R ^CX may be bonded to each other to form a ring, and two R ^IX may be bonded to each other to form a ring. R ^NX , R ^CX and R ^IX may each be bonded to one or two rings to which X containing itself is bonded,
At least one selected from the group consisting of an aryl ring and a heteroaryl ring in the formula (Int) may be condensed with at least one cycloalkane, and the cycloalkane may be substituted with at least one substituent. At least one -CH ₂ - in the cycloalkane may be substituted with -O-,
At least one hydrogen in the formula (Int) may be substituted with cyano, halogen, or deuterium. A compound represented by the formula (Int);

In the expression (Int),
Ring B, ring C, ring D, ring E, ring F, ring G, ring H, and ring I are each independently a substituted or unsubstituted aryl ring or a substituted or unsubstituted heteroaryl ring,
The broken line connecting the C ring and the D ring indicates that the C ring and the D ring are not bonded at the position of the dashed line, or are bonded through a single bond or linking group at the position of the broken line,
Z is -C(-R ^Z )= or -N=, R ^Z is hydrogen or a substituent,
X is ^each independently a single bond, > _NR ^NX , > ^O , >C ( _-R ^C It is substituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and R ^CX and R ^IX are each independently hydrogen, substituted or unsubstituted aryl, substituted or unsubstituted. It is substituted heteroaryl, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl, and two R ^CX may be bonded to each other to form a ring, and two R ^IX may be bonded to each other to form a ring. R ^NX , R ^CX and R ^IX may each be bonded to one or two rings to which X containing itself is bonded,
At least one selected from the group consisting of an aryl ring and a heteroaryl ring in the formula (Int) may be condensed with at least one cycloalkane, and the cycloalkane may be substituted with at least one substituent. At least one -CH ₂ - in the cycloalkane may be substituted with -O-,
At least one hydrogen in the formula (Int) may be substituted with cyano, halogen, or deuterium.