Compound, material for organic electroluminescence device, organic electroluminescence device and electronic device

Abstract

The present invention provides: a compound which further improves the performance of an organic EL element; an organic electroluminescent element which has further improved element performance; and an electronic device which comprises this organic electroluminescent element. A compound which is represented by formula (1), while having a molecular weight of 650 or more; an organic electroluminescent element which contains this compound; and an electronic device which comprises this organic electroluminescent element. (In the formula, Cz, n, Y1, Y2, Ar1, Ar2, L1, L2, L3, L4 and R1 to R6 are as defined in the description.)

Description

[Technical field]

[0001] The present invention relates to a compound, a material for an organic electroluminescence device, an organic electroluminescence device, and an electronic device including the organic electroluminescence device. [Background technology]

[0002] Generally, an organic electroluminescence element (hereinafter sometimes referred to as "organic EL element") is composed of an anode, a cathode, and an organic layer sandwiched between the anode and cathode. When a voltage is applied between the two electrodes, electrons are injected from the cathode side and holes are injected from the anode side into the light-emitting region, where they recombine to generate an excited state, and light is emitted when the excited state returns to the ground state. Therefore, the development of materials that efficiently transport electrons or holes to the light-emitting region and facilitate the recombination of electrons and holes is important for obtaining high-performance organic EL elements.

[0003] Patent Documents 1 to 9 disclose compounds used as materials for organic electroluminescence devices. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] WO2005 / 112519A1 [Patent Document 2] KR2014-0006708A [Patent Document 3] WO2017 / 200210A1 [Patent Document 4] WO2019 / 139419A1 [Patent Document 5] US2014 / 361268A1 [Patent Document 6] WO2018 / 105888A1 [Patent Document 7] CN107880031A [Patent Document 8] WO2018 / 056645A1 [Patent Document 9] WO2012 / 108881A1 Summary of the Invention [Problem to be solved by the invention]

[0005] Although many compounds for organic EL devices have been reported, there is still a demand for compounds that further improve the performance of organic EL devices.

[0006] The present invention has been made to solve the above-mentioned problems, and an object of the present invention is to provide a compound that further improves the performance of an organic EL device, an organic EL device having further improved device performance, and an electronic device including such an organic EL device. [Means for solving the problem]

[0007] The present inventors have conducted extensive research into the performance of organic EL devices containing the compounds described in Patent Documents 1 to 9, and as a result have found that a naphthylpyrimidine compound having a molecular weight of 650 or more and having a structure in which a specific carbazole skeleton is bonded to a pyrimidine skeleton via a single bond or an arylene group and further via a naphthylene group provides an organic EL device with improved device performance.

[0008] In one aspect, the present invention provides a compound represented by the following formula (1), wherein the molecular weight of the compound is 650 or more. [ka] (In the formula, Y 1 and Y 2 One of the is a nitrogen atom and the other is CR. R is selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a fluorine atom, and a cyano group; Ar 1 and Ar 2 are each independently selected from a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms and a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms; L 1 and L 2 each independently represents a single bond or a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms. R 1 ~R 6 are each independently selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a fluorine atom, and a cyano group; R 1 ~R 6 Adjacent two selected from the following do not bond to each other to form a ring. Cz is represented by the following formula (1-a) or formula (1-b): [ka] During the ceremony, R 21 ~R 28 and R 31 ~R 38 are each independently a hydrogen atom or a substituent, and the substituent is selected from a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms and not having a nitrogen-containing 5-membered ring or a nitrogen-containing 7-membered ring, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a fluorine atom, and a cyano group, However, R 21 ~R 28Two adjacent ones selected from R 31 ~R 38 Two adjacent ones selected from R 24 and R 25 and R 34 and R 35 do not bond to each other to form a ring. R a is selected from a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, and a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms; R 21 ~R 28 One selected from *a through L 3 is a single bond that connects to *b is L 3 represents the position at which the molecule binds to the molecule. n is an integer of 1 to 3, and when n is an integer of 2 or 3, two or three Cz's are the same or different from each other; L 3 and L 4 are each independently a single bond or a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms. However, when n is an integer of 2 or 3, L 4 is a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms.

[0009] In another aspect, the present invention provides a material for an organic EL device, comprising a compound represented by the above formula (1), the compound having a molecular weight of 650 or more.

[0010] In still another aspect, the present invention provides an organic electroluminescent device comprising an anode, a cathode, and an organic layer disposed between the anode and the cathode, the organic layer comprising an emitting layer, at least one layer of the organic layer comprising a compound represented by formula (1) above, the molecular weight of the compound being 650 or more.

[0011] In still another aspect, the present invention provides an electronic device including the organic electroluminescence device. Effect of the Invention

[0012] An organic EL device containing a compound represented by the above formula (1) having a molecular weight of 650 or more exhibits improved device performance. [Brief description of the drawings]

[0013] [Figure 1] FIG. 1 is a schematic diagram illustrating an example of a layer structure of an organic EL element according to one embodiment of the present invention. [Diagram 2] FIG. 2 is a schematic diagram showing another example of a layer structure of an organic EL element according to an embodiment of the present invention. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0014] [Definition] In this specification, hydrogen atoms include isotopes having different numbers of neutrons, namely protium, deuterium, and tritium.

[0015] In the present specification, in a chemical structural formula, a hydrogen atom, i.e., a protium atom, a deuterium atom, or a tritium atom is assumed to be bonded to a possible bonding position that is not explicitly indicated with a symbol such as "R" or "D" representing a deuterium atom.

[0016] In this specification, the number of ring carbon atoms represents the number of carbon atoms among the atoms constituting the ring itself of a compound having a structure in which atoms are bonded in a ring (for example, a monocyclic compound, a condensed ring compound, a bridged compound, a carbocyclic compound, and a heterocyclic compound). When the ring is substituted with a substituent, the carbon contained in the substituent is not included in the number of ring carbon atoms. The "number of ring carbon atoms" described below is the same unless otherwise specified. For example, a benzene ring has 6 ring carbon atoms, a naphthalene ring has 10 ring carbon atoms, a pyridine ring has 5 ring carbon atoms, and a furan ring has 4 ring carbon atoms. For example, the number of ring carbon atoms of a 9,9-diphenylfluorenyl group is 13, and the number of ring carbon atoms of a 9,9'-spirobifluorenyl group is 25. In addition, when a benzene ring is substituted with, for example, an alkyl group as a substituent, the carbon number of the alkyl group is not included in the number of ring carbon atoms of the benzene ring. Therefore, the number of ring carbon atoms of the benzene ring substituted with an alkyl group is 6. In addition, when a naphthalene ring is substituted with, for example, an alkyl group as a substituent, the carbon number of the alkyl group is not included in the number of ring carbon atoms of the naphthalene ring. Therefore, the number of ring carbon atoms of the naphthalene ring substituted with an alkyl group is 10.

[0017] In this specification, the number of ring atoms refers to the number of atoms constituting the ring itself of a compound (e.g., a monocyclic compound, a fused ring compound, a bridged compound, a carbocyclic compound, and a heterocyclic compound) having a structure in which atoms are bonded in a ring (e.g., a monocyclic compound, a fused ring compound, and a ring assembly). The number of ring atoms does not include atoms that do not constitute a ring (e.g., a hydrogen atom that terminates the bond of an atom constituting a ring) or atoms contained in a substituent when the ring is substituted with a substituent. The "number of ring atoms" described below is the same unless otherwise specified. For example, the number of ring atoms of a pyridine ring is 6, the number of ring atoms of a quinazoline ring is 10, and the number of ring atoms of a furan ring is 5. For example, the number of hydrogen atoms or atoms constituting a substituent bonded to a pyridine ring is not included in the number of pyridine ring atoms. Therefore, the number of ring atoms of a pyridine ring to which a hydrogen atom or a substituent is bonded is 6. For example, hydrogen atoms bonded to carbon atoms of a quinazoline ring or atoms constituting a substituent are not included in the number of ring atoms of the quinazoline ring. Therefore, the number of ring atoms of a quinazoline ring to which a hydrogen atom or a substituent is bonded is 10.

[0018] In the present specification, the "number of carbon atoms XX to YY" in the expression "a substituted or unsubstituted ZZ group having carbon atoms XX to YY" represents the number of carbon atoms when the ZZ group is unsubstituted, and does not include the number of carbon atoms of the substituent when the ZZ group is substituted. Here, "YY" is larger than "XX", "XX" means an integer of 1 or more, and "YY" means an integer of 2 or more.

[0019] In the present specification, the "number of atoms XX to YY" in the expression "a substituted or unsubstituted ZZ group having the number of atoms XX to YY" represents the number of atoms when the ZZ group is unsubstituted, and does not include the number of atoms of the substituent when the ZZ group is substituted. Here, "YY" is larger than "XX", "XX" means an integer of 1 or more, and "YY" means an integer of 2 or more.

[0020] In this specification, the term "unsubstituted ZZ group" refers to the case where a "substituted or unsubstituted ZZ group" is an "unsubstituted ZZ group", and the term "substituted ZZ group" refers to the case where a "substituted or unsubstituted ZZ group" is a "substituted ZZ group". In the present specification, "unsubstituted" in the case of "a substituted or unsubstituted ZZ group" means that a hydrogen atom in the ZZ group is not replaced with a substituent. The hydrogen atom in the "unsubstituted ZZ group" is a protium atom, a deuterium atom, or a tritium atom. In the present specification, "substituted" in the case of "a substituted or unsubstituted ZZ group" means that one or more hydrogen atoms in the ZZ group are replaced with a substituent. Similarly, "substituted" in the case of "a BB group substituted with an AA group" means that one or more hydrogen atoms in the BB group are replaced with an AA group.

[0021] "Substituents Described Herein" The substituents described in this specification will be described below.

[0022] The "unsubstituted aryl group" described in this specification has 6 to 50 ring carbon atoms, preferably 6 to 30, and more preferably 6 to 18 ring carbon atoms, unless otherwise specified in this specification. The "unsubstituted heterocyclic group" described in this specification has 5 to 50 ring atoms, preferably 5 to 30, and more preferably 5 to 18 ring atoms, unless otherwise specified in this specification. The "unsubstituted alkyl group" described in this specification has 1 to 50 carbon atoms, preferably 1 to 20 carbon atoms, and more preferably 1 to 6 carbon atoms, unless otherwise specified in this specification. The "unsubstituted alkenyl group" described in this specification has 2 to 50 carbon atoms, preferably 2 to 20 carbon atoms, and more preferably 2 to 6 carbon atoms, unless otherwise specified in this specification. The "unsubstituted alkynyl group" described in this specification has 2 to 50 carbon atoms, preferably 2 to 20 carbon atoms, and more preferably 2 to 6 carbon atoms, unless otherwise specified in this specification. The "unsubstituted cycloalkyl group" described in this specification has 3 to 50 ring carbon atoms, preferably 3 to 20, and more preferably 3 to 6 ring carbon atoms, unless otherwise specified in this specification. The "unsubstituted arylene group" described in this specification has 6 to 50 ring carbon atoms, preferably 6 to 30, and more preferably 6 to 18 ring carbon atoms, unless otherwise specified in this specification. The "unsubstituted divalent heterocyclic group" described in this specification has 5 to 50 ring atoms, preferably 5 to 30, and more preferably 5 to 18 ring atoms, unless otherwise specified in this specification. The "unsubstituted alkylene group" described in this specification has 1 to 50 carbon atoms, preferably 1 to 20 carbon atoms, and more preferably 1 to 6 carbon atoms, unless otherwise specified in this specification.

[0023] "Substituted or unsubstituted aryl groups" Specific examples (specific example group G1) of the "substituted or unsubstituted aryl group" described in this specification include the following unsubstituted aryl group (specific example group G1A) and substituted aryl group (specific example group G1B). (Here, the unsubstituted aryl group refers to the case where the "substituted or unsubstituted aryl group" is an "unsubstituted aryl group", and the substituted aryl group refers to the case where the "substituted or unsubstituted aryl group" is a "substituted aryl group".) In this specification, when the term "aryl group" is simply used, it includes both an "unsubstituted aryl group" and a "substituted aryl group". The term "substituted aryl group" refers to a group in which one or more hydrogen atoms of an "unsubstituted aryl group" are replaced with a substituent. Examples of the "substituted aryl group" include the "unsubstituted aryl group" in the specific example group G1A below in which one or more hydrogen atoms are replaced with a substituent, and the substituted aryl group in the specific example group G1B below. The examples of the "unsubstituted aryl group" and the examples of the "substituted aryl group" listed here are merely examples, and the "substituted aryl group" described in this specification also includes the "substituted aryl group" in the specific example group G1B below in which a hydrogen atom bonded to a carbon atom of the aryl group itself is further replaced with a substituent, and the "substituted aryl group" in the specific example group G1B below in which a hydrogen atom of a substituent is further replaced with a substituent.

[0024] Unsubstituted aryl groups (specific example group G1A): Phenyl group, p-biphenyl group, m-biphenyl group, o-biphenyl group, p-terphenyl-4-yl group, p-terphenyl-3-yl group, p-terphenyl-2-yl group, m-terphenyl-4-yl group, m-terphenyl-3-yl group, m-terphenyl-2-yl group, o-terphenyl-4-yl group, o-terphenyl-3-yl group, o-terphenyl-2-yl group, 1-naphthyl group, 2-naphthyl group, anthryl group, Benzanthryl group, A phenanthryl group, Benzophenanthryl group, A phenalenyl group, Pyrenyl group, Chrysenyl group, benzochrysenyl group, A triphenylenyl group, Benzotriphenylenyl group, tetracenyl group, Pentacenyl group, fluorenyl group, 9,9'-spirobifluorenyl group, Benzofluorenyl group, Dibenzofluorenyl group, fluoranthenyl group, Benzofluoranthenyl group, Perylenyl groups, and A monovalent aryl group derived by removing one hydrogen atom from a ring structure represented by the following general formulas (TEMP-1) to (TEMP-15).

[0025] [ka]

[0026] [ka]

[0027] Substituted aryl groups (specific example group G1B): o-tolyl group, m-tolyl group, p-tolyl group, para-xylyl group, meta-xylyl group, ortho-xylyl group, para-isopropylphenyl group, meta-isopropylphenyl group, ortho-isopropylphenyl group, para-t-butylphenyl group, meta-t-butylphenyl group, ortho-t-butylphenyl group, 3,4,5-trimethylphenyl group, 9,9-dimethylfluorenyl group, 9,9-diphenylfluorenyl group 9,9-bis(4-methylphenyl)fluorenyl group, 9,9-bis(4-isopropylphenyl)fluorenyl group, 9,9-bis(4-t-butylphenyl)fluorenyl group, Cyanophenyl group, triphenylsilylphenyl group, trimethylsilylphenyl group, phenylnaphthyl group, naphthylphenyl group, and A group in which one or more hydrogen atoms of a monovalent group derived from a ring structure represented by any one of the general formulae (TEMP-1) to (TEMP-15) are replaced with a substituent.

[0028] "Substituted or unsubstituted heterocyclic groups" The "heterocyclic group" described herein is a cyclic group containing at least one heteroatom as a ring-forming atom. Specific examples of the heteroatom include a nitrogen atom, an oxygen atom, a sulfur atom, a silicon atom, a phosphorus atom, and a boron atom. The "heterocyclic groups" described herein are either monocyclic or fused ring groups. The "heterocyclic group" described herein may be an aromatic heterocyclic group or a non-aromatic heterocyclic group. Specific examples (specific example group G2) of the "substituted or unsubstituted heterocyclic group" described in this specification include the following unsubstituted heterocyclic group (specific example group G2A) and substituted heterocyclic group (specific example group G2B). (Here, the unsubstituted heterocyclic group refers to the case where the "substituted or unsubstituted heterocyclic group" is an "unsubstituted heterocyclic group", and the substituted heterocyclic group refers to the case where the "substituted or unsubstituted heterocyclic group" is a "substituted heterocyclic group".) In this specification, when the term "heterocyclic group" is simply used, it includes both an "unsubstituted heterocyclic group" and a "substituted heterocyclic group". The term "substituted heterocyclic group" refers to a group in which one or more hydrogen atoms of an "unsubstituted heterocyclic group" are replaced with a substituent. Specific examples of the "substituted heterocyclic group" include the groups in which the hydrogen atoms of the "unsubstituted heterocyclic group" in the specific example group G2A below are replaced, and the examples of the substituted heterocyclic group in the specific example group G2B below are exemplified. The examples of the "unsubstituted heterocyclic group" and the examples of the "substituted heterocyclic group" listed here are merely examples, and the "substituted heterocyclic group" described in this specification also includes the groups in which the hydrogen atoms bonded to the ring-forming atoms of the heterocyclic group itself in the "substituted heterocyclic group" in the specific example group G2B are further replaced with a substituent, and the groups in which the hydrogen atoms of the substituents in the "substituted heterocyclic group" in the specific example group G2B are further replaced with a substituent.

[0029] The specific example group G2A includes, for example, the following unsubstituted heterocyclic groups containing a nitrogen atom (specific example group G2A1), unsubstituted heterocyclic groups containing an oxygen atom (specific example group G2A2), unsubstituted heterocyclic groups containing a sulfur atom (specific example group G2A3), and monovalent heterocyclic groups derived by removing one hydrogen atom from ring structures represented by the following general formulae (TEMP-16) to (TEMP-33) (specific example group G2A4).

[0030] Specific example group G2B includes, for example, the following nitrogen atom-containing substituted heterocyclic groups (specific example group G2B1), oxygen atom-containing substituted heterocyclic groups (specific example group G2B2), sulfur atom-containing substituted heterocyclic groups (specific example group G2B3), and monovalent heterocyclic groups derived from ring structures represented by the following general formulae (TEMP-16) to (TEMP-33), in which one or more hydrogen atoms are replaced with substituents (specific example group G2B4).

[0031] Unsubstituted heterocyclic groups containing a nitrogen atom (specific example group G2A1): Pyrrolyl group, imidazolyl group, A pyrazolyl group, A triazolyl group, Tetrazolyl group, oxazolyl group, an isoxazolyl group, oxadiazolyl group, A thiazolyl group, isothiazolyl group, A thiadiazolyl group, Pyridyl group, pyridazinyl group, pyrimidinyl group, A pyrazinyl group, Triazinyl group, Indolyl groups, isoindolyl group, Indolizinyl group, A quinolizinyl group, A quinolyl group, isoquinolyl group, Cinnolyl group, phthalazinyl group, A quinazolinyl group, A quinoxalinyl group, Benzimidazolyl group, Indazolyl group, A phenanthrolinyl group, A phenanthridinyl group, acridinyl group, A phenazinyl group, A carbazolyl group, Benzocarbazolyl group, morpholino group, phenoxazinyl group, A phenothiazinyl group, Azacarbazolyl and diazacarbazolyl groups.

[0032] Unsubstituted heterocyclic groups containing an oxygen atom (specific example group G2A2): Furyl group, oxazolyl group, an isoxazolyl group, oxadiazolyl group, xanthenyl group, benzofuranyl group, isobenzofuranyl group, Dibenzofuranyl group, naphthobenzofuranyl group, benzoxazolyl group, benzoisoxazolyl group, phenoxazinyl group, morpholino group, Dinaphthofuranyl group, azadibenzofuranyl group, diazadibenzofuranyl group, Azanaphthobenzofuranyl groups, and Diazanaphthobenzofuranyl group.

[0033] Unsubstituted heterocyclic groups containing a sulfur atom (specific example group G2A3): A thienyl group, A thiazolyl group, isothiazolyl group, A thiadiazolyl group, Benzothiophenyl group (benzothienyl group), Isobenzothiophenyl group (isobenzothienyl group), Dibenzothiophenyl group (dibenzothienyl group), Naphthobenzothiophenyl group (naphthobenzothienyl group), benzothiazolyl group, Benzisothiazolyl group, A phenothiazinyl group, Dinaphthothiophenyl group (dinaphthothienyl group), Azadibenzothiophenyl group (azadibenzothienyl group), Diazadibenzothiophenyl group (diazadibenzothienyl group), Azanapthobenzothiophenyl group (azanaphthobenzothienyl group), and Diazanaphthobenzothiophenyl group (diazanaphthobenzothienyl group).

[0034] Monovalent heterocyclic groups derived by removing one hydrogen atom from the ring structures represented by the following general formulae (TEMP-16) to (TEMP-33) (specific example group G2A4):

[0035] [ka]

[0036] [ka]

[0037] In the general formulae (TEMP-16) to (TEMP-33), X A and Y A are each independently an oxygen atom, a sulfur atom, NH, or CH2. A and Y A At least one of is an oxygen atom, a sulfur atom, or NH. In the general formulae (TEMP-16) to (TEMP-33), X A and Y A When at least one of is NH or CH2, the monovalent heterocyclic group derived from the ring structure represented by the general formulas (TEMP-16) to (TEMP-33) includes a monovalent group obtained by removing one hydrogen atom from NH or CH2.

[0038] Substituted heterocyclic groups containing a nitrogen atom (specific example group G2B1): A (9-phenyl)carbazolyl group, (9-biphenylyl)carbazolyl group, (9-phenyl)phenylcarbazolyl group, (9-naphthyl)carbazolyl group, diphenylcarbazol-9-yl group, phenylcarbazol-9-yl group, methylbenzimidazolyl group, Ethyl benzimidazolyl group, phenyltriazinyl group, Biphenylyltriazinyl group, Diphenyltriazinyl group, phenylquinazolinyl group, and Biphenylylquinazolinyl group.

[0039] Substituted heterocyclic groups containing an oxygen atom (specific example group G2B2): phenyldibenzofuranyl group, methyldibenzofuranyl group, t-butyldibenzofuranyl group, and A monovalent residue of spiro[9H-xanthene-9,9'-[9H]fluorene].

[0040] Substituted heterocyclic groups containing sulfur atoms (specific example group G2B3): Phenyldibenzothiophenyl group, methyldibenzothiophenyl group, t-Butyldibenzothiophenyl group, and A monovalent residue of spiro[9H-thioxanthene-9,9'-[9H]fluorene].

[0041] Groups in which one or more hydrogen atoms of a monovalent heterocyclic group derived from a ring structure represented by the above general formulae (TEMP-16) to (TEMP-33) are replaced with a substituent (specific example group G2B4):

[0042] The above "one or more hydrogen atoms of a monovalent heterocyclic group" means one or more hydrogen atoms selected from a hydrogen atom bonded to a ring-forming carbon atom of the monovalent heterocyclic group, a hydrogen atom bonded to a nitrogen atom when at least one of XA and YA is NH, and a hydrogen atom of a methylene group when one of XA and YA is CH2.

[0043] "Substituted or unsubstituted alkyl groups" Specific examples (specific example group G3) of the "substituted or unsubstituted alkyl group" described in this specification include the following unsubstituted alkyl group (specific example group G3A) and substituted alkyl group (specific example group G3B). (Here, the unsubstituted alkyl group refers to the case where the "substituted or unsubstituted alkyl group" is an "unsubstituted alkyl group", and the substituted alkyl group refers to the case where the "substituted or unsubstituted alkyl group" is a "substituted alkyl group".) Hereinafter, when the term "alkyl group" is simply mentioned, it includes both the "unsubstituted alkyl group" and the "substituted alkyl group". The term "substituted alkyl group" refers to a group in which one or more hydrogen atoms in the "unsubstituted alkyl group" are replaced with a substituent. Specific examples of the "substituted alkyl group" include the following "unsubstituted alkyl group" (specific example group G3A) in which one or more hydrogen atoms are replaced with a substituent, and examples of the substituted alkyl group (specific example group G3B). In this specification, the alkyl group in the "unsubstituted alkyl group" refers to a chain-like alkyl group. Therefore, the "unsubstituted alkyl group" includes a straight-chain "unsubstituted alkyl group" and a branched "unsubstituted alkyl group". Note that the examples of the "unsubstituted alkyl group" and the examples of the "substituted alkyl group" listed here are merely examples, and the "substituted alkyl group" described in this specification also includes a group in which a hydrogen atom of the alkyl group itself in the "substituted alkyl group" in the specific example group G3B is further replaced with a substituent, and a group in which a hydrogen atom of a substituent in the "substituted alkyl group" in the specific example group G3B is further replaced with a substituent.

[0044] Unsubstituted alkyl groups (specific example group G3A): Methyl group, Ethyl group, n-propyl group, isopropyl group, n-Butyl group, isobutyl group, s-Butyl group, and t-Butyl group.

[0045] Substituted alkyl groups (specific example group G3B): Heptafluoropropyl group (including isomers), pentafluoroethyl group, 2,2,2-trifluoroethyl group, and Trifluoromethyl group.

[0046] "Substituted or unsubstituted alkenyl group" Specific examples (specific example group G4) of the "substituted or unsubstituted alkenyl group" described in this specification include the following unsubstituted alkenyl group (specific example group G4A) and substituted alkenyl group (specific example group G4B). (Here, the unsubstituted alkenyl group refers to the case where the "substituted or unsubstituted alkenyl group" is an "unsubstituted alkenyl group", and the "substituted alkenyl group" refers to the case where the "substituted or unsubstituted alkenyl group" is a "substituted alkenyl group".) In this specification, the term "alkenyl group" simply includes both an "unsubstituted alkenyl group" and a "substituted alkenyl group". The term "substituted alkenyl group" refers to a group in which one or more hydrogen atoms in an "unsubstituted alkenyl group" are replaced with a substituent. Specific examples of the "substituted alkenyl group" include the following "unsubstituted alkenyl group" (specific example group G4A) having a substituent, and examples of substituted alkenyl groups (specific example group G4B). The examples of the "unsubstituted alkenyl group" and the examples of the "substituted alkenyl group" listed here are merely examples, and the "substituted alkenyl group" described in this specification also includes a group in which a hydrogen atom of the alkenyl group itself in the "substituted alkenyl group" in specific example group G4B is further replaced with a substituent, and a group in which a hydrogen atom of a substituent in the "substituted alkenyl group" in specific example group G4B is further replaced with a substituent.

[0047] Unsubstituted alkenyl groups (specific example group G4A): Vinyl group, Allyl groups, 1-butenyl group, 2-butenyl group, and 3-Butenyl group.

[0048] Substituted alkenyl groups (specific example group G4B): 1,3-butanedienyl group, 1-methylvinyl group, 1-methylallyl group, 1,1-dimethylallyl group, 2-methylallyl group, and 1,2-Dimethylallyl group.

[0049] "Substituted or unsubstituted alkynyl groups" Specific examples (specific example group G5) of the "substituted or unsubstituted alkynyl group" described in this specification include the following unsubstituted alkynyl groups (specific example group G5A). (Here, the unsubstituted alkynyl group refers to the case where the "substituted or unsubstituted alkynyl group" is an "unsubstituted alkynyl group".) Hereinafter, when simply referring to an "alkynyl group", it includes both an "unsubstituted alkynyl group" and a "substituted alkynyl group". The term "substituted alkynyl group" refers to an "unsubstituted alkynyl group" in which one or more hydrogen atoms have been replaced with a substituent. Specific examples of the "substituted alkynyl group" include the following "unsubstituted alkynyl groups" (specific example group G5A) in which one or more hydrogen atoms have been replaced with a substituent.

[0050] Unsubstituted alkynyl groups (specific example group G5A): Ethynyl group

[0051] "Substituted or unsubstituted cycloalkyl groups" Specific examples (specific example group G6) of the "substituted or unsubstituted cycloalkyl group" described in this specification include the following unsubstituted cycloalkyl group (specific example group G6A) and substituted cycloalkyl group (specific example group G6B). (Here, the unsubstituted cycloalkyl group refers to the case where the "substituted or unsubstituted cycloalkyl group" is an "unsubstituted cycloalkyl group", and the substituted cycloalkyl group refers to the case where the "substituted or unsubstituted cycloalkyl group" is a "substituted cycloalkyl group".) In this specification, when the term "cycloalkyl group" is simply used, it includes both an "unsubstituted cycloalkyl group" and a "substituted cycloalkyl group". The term "substituted cycloalkyl group" refers to a group in which one or more hydrogen atoms in the "unsubstituted cycloalkyl group" are replaced with a substituent. Specific examples of the "substituted cycloalkyl group" include the following "unsubstituted cycloalkyl group" (specific example group G6A) in which one or more hydrogen atoms are replaced with a substituent, and the examples of the substituted cycloalkyl group (specific example group G6B). The examples of the "unsubstituted cycloalkyl group" and the examples of the "substituted cycloalkyl group" listed here are merely examples, and the "substituted cycloalkyl group" described in this specification also includes a group in the "substituted cycloalkyl group" in the specific example group G6B in which one or more hydrogen atoms bonded to a carbon atom of the cycloalkyl group itself are replaced with a substituent, and a group in the "substituted cycloalkyl group" in the specific example group G6B in which a hydrogen atom of a substituent is further replaced with a substituent.

[0052] Unsubstituted cycloalkyl groups (specific example group G6A): A cyclopropyl group, A cyclobutyl group, Cyclopentyl group, cyclohexyl group, 1-adamantyl group, 2-adamantyl group, 1-norbornyl group, and 2-Norbornyl group.

[0053] Substituted cycloalkyl groups (specific example group G6B): 4-Methylcyclohexyl group.

[0054] -Si(R 901 )(R 902 )(R 903 ) a group represented by As described herein, -Si(R 901 )(R 902 )(R 903 Specific examples (specific example group G7) of the group represented by -Si(G1)(G1)(G1), -Si(G1)(G2)(G2), -Si(G1)(G1)(G2), -Si(G2)(G2)(G2), -Si(G3)(G3)(G3), and -Si(G6)(G6)(G6) Here, G1 is a "substituted or unsubstituted aryl group" described in specific example group G1. G2 is a "substituted or unsubstituted heterocyclic group" described in specific example group G2. G3 is a "substituted or unsubstituted alkyl group" described in specific example group G3. G6 is a "substituted or unsubstituted cycloalkyl group" described in specific example group G6. The multiple G1s in -Si(G1)(G1)(G1) are the same as or different from each other. The multiple G2s in -Si(G1)(G2)(G2) are the same as or different from each other. The multiple G1s in -Si(G1)(G1)(G2) are the same as or different from each other. The multiple G2s in -Si(G2)(G2)(G2) are the same as or different from each other. The multiple G3s in -Si(G3)(G3)(G3) are the same as or different from each other. The multiple G6s in -Si(G6)(G6)(G6) are the same as or different from each other.

[0055] -O-(R 904 ) a group represented by As described herein, -O-(R 904 Specific examples (specific example group G8) of the group represented by -O(G1), -O(G2), -O(G3), and -O(G6) Examples include: Where: G1 is a "substituted or unsubstituted aryl group" described in specific example group G1. G2 is a "substituted or unsubstituted heterocyclic group" described in specific example group G2. G3 is a "substituted or unsubstituted alkyl group" described in specific example group G3. G6 is a "substituted or unsubstituted cycloalkyl group" described in specific example group G6.

[0056] -S-(R 905 ) a group represented by As described herein, -S-(R 905 Specific examples (specific example group G9) of the group represented by -S(G1), -S(G2), -S(G3), and -S(G6) Examples include: Where: G1 is a "substituted or unsubstituted aryl group" described in specific example group G1. G2 is a "substituted or unsubstituted heterocyclic group" described in specific example group G2. G3 is a "substituted or unsubstituted alkyl group" described in specific example group G3. G6 is a "substituted or unsubstituted cycloalkyl group" described in specific example group G6.

[0057] -N(R 906 )(R 907 ) a group represented by As described herein, -N(R 906 )(R 907 Specific examples (specific example group G10) of the group represented by -N(G1)(G1), -N(G2)(G2), -N(G1)(G2), -N(G3)(G3), and -N(G6)(G6) Examples include: Where: G1 is a "substituted or unsubstituted aryl group" described in specific example group G1. G2 is a "substituted or unsubstituted heterocyclic group" described in specific example group G2. G3 is a "substituted or unsubstituted alkyl group" described in specific example group G3. G6 is a "substituted or unsubstituted cycloalkyl group" described in specific example group G6. -The multiple G1's in N(G1)(G1) are the same or different from each other. -The multiple G2's in N(G2)(G2) are the same or different from each other. -The multiple G3's in N(G3)(G3) are the same or different from each other. The multiple G6s in -N(G6)(G6) are the same or different from each other.

[0058] "Halogen atoms" Specific examples of the "halogen atom" described in this specification (specific example group G11) include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.

[0059] "Substituted or unsubstituted fluoroalkyl groups" The term "substituted or unsubstituted fluoroalkyl group" as used herein means a group in which at least one hydrogen atom bonded to a carbon atom constituting the alkyl group in the "substituted or unsubstituted alkyl group" is replaced with a fluorine atom, and also includes a group (perfluoro group) in which all hydrogen atoms bonded to carbon atoms constituting the alkyl group in the "substituted or unsubstituted alkyl group" are replaced with fluorine atoms. The number of carbon atoms in the "unsubstituted fluoroalkyl group" is 1 to 50, preferably 1 to 30, and more preferably 1 to 18, unless otherwise specified in the present specification. The term "substituted fluoroalkyl group" means a group in which one or more hydrogen atoms in the "fluoroalkyl group" are replaced with a substituent. The term "substituted fluoroalkyl group" as used herein also includes a group in which one or more hydrogen atoms bonded to a carbon atom in the alkyl chain in the "substituted fluoroalkyl group" are further replaced with a substituent, and a group in which one or more hydrogen atoms in the substituent in the "substituted fluoroalkyl group" are further replaced with a substituent. Specific examples of the "unsubstituted fluoroalkyl group" include the examples of the group in which one or more hydrogen atoms in the "alkyl group" (specific example group G3) are replaced with a fluorine atom.

[0060] "Substituted or unsubstituted haloalkyl groups" The term "substituted or unsubstituted haloalkyl group" as used herein means a group in which at least one hydrogen atom bonded to a carbon atom constituting the alkyl group in the "substituted or unsubstituted alkyl group" is replaced with a halogen atom, and also includes a group in which all hydrogen atoms bonded to carbon atoms constituting the alkyl group in the "substituted or unsubstituted alkyl group" are replaced with halogen atoms. The number of carbon atoms in the "unsubstituted haloalkyl group" is 1 to 50, preferably 1 to 30, and more preferably 1 to 18, unless otherwise specified in the present specification. The term "substituted haloalkyl group" means a group in which one or more hydrogen atoms in the "haloalkyl group" are replaced with a substituent. The term "substituted haloalkyl group" as used herein also includes a group in which one or more hydrogen atoms bonded to a carbon atom in the alkyl chain in the "substituted haloalkyl group" are further replaced with a substituent, and a group in which one or more hydrogen atoms in the substituent in the "substituted haloalkyl group" are further replaced with a substituent. Specific examples of the "unsubstituted haloalkyl group" include the examples of the group in which one or more hydrogen atoms in the "alkyl group" (specific example group G3) are replaced with a halogen atom. Haloalkyl groups are sometimes referred to as halogenated alkyl groups.

[0061] "Substituted or unsubstituted alkoxy groups" A specific example of the "substituted or unsubstituted alkoxy group" described in this specification is a group represented by -O(G3), where G3 is the "substituted or unsubstituted alkyl group" described in specific example group G3. The number of carbon atoms in the "unsubstituted alkoxy group" is 1 to 50, preferably 1 to 30, and more preferably 1 to 18, unless otherwise specified in this specification.

[0062] "Substituted or unsubstituted alkylthio groups" A specific example of the "substituted or unsubstituted alkylthio group" described in this specification is a group represented by -S(G3), where G3 is the "substituted or unsubstituted alkyl group" described in specific example group G3. The number of carbon atoms in the "unsubstituted alkylthio group" is 1 to 50, preferably 1 to 30, and more preferably 1 to 18, unless otherwise specified in this specification.

[0063] "Substituted or unsubstituted aryloxy group" A specific example of the "substituted or unsubstituted aryloxy group" described in this specification is a group represented by -O(G1), where G1 is a "substituted or unsubstituted aryl group" described in specific example group G1. The number of ring carbon atoms of the "unsubstituted aryloxy group" is 6 to 50, preferably 6 to 30, and more preferably 6 to 18, unless otherwise specified in this specification.

[0064] "Substituted or unsubstituted arylthio group" A specific example of the "substituted or unsubstituted arylthio group" described in this specification is a group represented by -S(G1), where G1 is a "substituted or unsubstituted aryl group" described in specific example group G1. The number of ring carbon atoms of the "unsubstituted arylthio group" is 6 to 50, preferably 6 to 30, and more preferably 6 to 18, unless otherwise specified in this specification.

[0065] "Substituted or unsubstituted trialkylsilyl group" A specific example of the "trialkylsilyl group" described in this specification is a group represented by -Si(G3)(G3)(G3), where G3 is a "substituted or unsubstituted alkyl group" described in the specific example group G3. The multiple G3s in -Si(G3)(G3)(G3) are the same or different from each other. The number of carbon atoms in each alkyl group of the "trialkylsilyl group" is 1 to 50, preferably 1 to 20, and more preferably 1 to 6, unless otherwise specified in this specification.

[0066] "Substituted or unsubstituted aralkyl group" A specific example of the "substituted or unsubstituted aralkyl group" described in the present specification is a group represented by -(G3)-(G1), where G3 is a "substituted or unsubstituted alkyl group" described in the specific example group G3, and G1 is a "substituted or unsubstituted aryl group" described in the specific example group G1. Thus, the "aralkyl group" is a group in which a hydrogen atom of an "alkyl group" is replaced with an "aryl group" as a substituent, and is one aspect of a "substituted alkyl group". The "unsubstituted aralkyl group" is an "unsubstituted alkyl group" substituted with an "unsubstituted aryl group", and the carbon number of the "unsubstituted aralkyl group" is 7 to 50, preferably 7 to 30, and more preferably 7 to 18, unless otherwise specified in the present specification. Specific examples of "substituted or unsubstituted aralkyl groups" include benzyl, 1-phenylethyl, 2-phenylethyl, 1-phenylisopropyl, 2-phenylisopropyl, phenyl-t-butyl, α-naphthylmethyl, 1-α-naphthylethyl, 2-α-naphthylethyl, 1-α-naphthylisopropyl, 2-α-naphthylisopropyl, β-naphthylmethyl, 1-β-naphthylethyl, 2-β-naphthylethyl, 1-β-naphthylisopropyl, and 2-β-naphthylisopropyl.

[0067] Unless otherwise specified in the present specification, the substituted or unsubstituted aryl group described in the present specification is preferably a phenyl group, a p-biphenyl group, a m-biphenyl group, an o-biphenyl group, a p-terphenyl-4-yl group, a p-terphenyl-3-yl group, a p-terphenyl-2-yl group, a m-terphenyl-4-yl group, a m-terphenyl-3-yl group, a m-terphenyl-2-yl group, an o-terphenyl-4-yl group, an o-terphenyl-3-yl group, an o-terphenyl-2-yl group, a 1-naphthyl group, a 2-naphthyl group, an anthryl group, a phenanthryl group, a pyrenyl group, a chrysenyl group, a triphenylenyl group, a fluorenyl group, a 9,9'-spirobifluorenyl group, a 9,9-dimethylfluorenyl group, a 9,9-diphenylfluorenyl group, and the like.

[0068] The substituted or unsubstituted heterocyclic group described in the present specification, unless otherwise specified in the present specification, is preferably a pyridyl group, a pyrimidinyl group, a triazinyl group, a quinolyl group, an isoquinolyl group, a quinazolinyl group, a benzimidazolyl group, a phenanthrolinyl group, a carbazolyl group (a 1-carbazolyl group, a 2-carbazolyl group, a 3-carbazolyl group, a 4-carbazolyl group, or a 9-carbazolyl group), a benzocarbazolyl group, an azacarbazolyl group, a diazacarbazolyl group, a dibenzofuranyl group, a naphthobenzofuranyl group, an azadibenzofuranyl group, a diazadibenzofuranyl group, a dibenzothiophenyl group, a naphthobenzothiophenyl group, an aza Examples of such groups include a dibenzothiophenyl group, a diazadibenzothiophenyl group, a (9-phenyl)carbazolyl group (a (9-phenyl)carbazol-1-yl group, a (9-phenyl)carbazol-2-yl group, a (9-phenyl)carbazol-3-yl group, or a (9-phenyl)carbazol-4-yl group), a (9-biphenylyl)carbazolyl group, a (9-phenyl)phenylcarbazolyl group, a diphenylcarbazol-9-yl group, a phenylcarbazol-9-yl group, a phenyltriazinyl group, a biphenylyltriazinyl group, a diphenyltriazinyl group, a phenyldibenzofuranyl group, and a phenyldibenzothiophenyl group.

[0069] In this specification, a carbazolyl group is specifically any of the following groups, unless otherwise specified in the specification.

[0070] [ka]

[0071] In this specification, the (9-phenyl)carbazolyl group is specifically any of the following groups, unless otherwise specified in the specification.

[0072] [ka]

[0073] In the general formulae (TEMP-Cz1) to (TEMP-Cz9), * represents a bonding position.

[0074] In this specification, a dibenzofuranyl group and a dibenzothiophenyl group are specifically any of the following groups, unless otherwise specified in this specification.

[0075] [ka]

[0076] In the above general formulae (TEMP-34) to (TEMP-41), * represents a bonding position.

[0077] The substituted or unsubstituted alkyl groups described herein are preferably methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, and the like, unless otherwise specified herein.

[0078] "Substituted or unsubstituted arylene group" Unless otherwise specified, the "substituted or unsubstituted arylene group" described in this specification is a divalent group derived by removing one hydrogen atom on the aryl ring from the above-mentioned "substituted or unsubstituted aryl group". Specific examples of the "substituted or unsubstituted arylene group" (specific example group G12) include divalent groups derived by removing one hydrogen atom on the aryl ring from the "substituted or unsubstituted aryl group" described in specific example group G1.

[0079] "Substituted or unsubstituted divalent heterocyclic group" Unless otherwise specified, the "substituted or unsubstituted divalent heterocyclic group" described in this specification is a divalent group derived by removing one hydrogen atom on the heterocycle from the above-mentioned "substituted or unsubstituted heterocyclic group". Specific examples of the "substituted or unsubstituted divalent heterocyclic group" (specific example group G13) include divalent groups derived by removing one hydrogen atom on the heterocycle from the "substituted or unsubstituted heterocyclic group" described in specific example group G2.

[0080] "Substituted or unsubstituted alkylene group" Unless otherwise specified, the "substituted or unsubstituted alkylene group" described in this specification is a divalent group derived by removing one hydrogen atom on the alkyl chain from the above-mentioned "substituted or unsubstituted alkyl group". Specific examples of the "substituted or unsubstituted alkylene group" (specific example group G14) include divalent groups derived by removing one hydrogen atom on the alkyl chain from the "substituted or unsubstituted alkyl group" described in specific example group G3.

[0081] The substituted or unsubstituted arylene group described in this specification is preferably any of the groups represented by the following general formulae (TEMP-42) to (TEMP-68), unless otherwise specified in this specification.

[0082] [ka]

[0083] [ka]

[0084] In the general formulae (TEMP-42) to (TEMP-52), Q1 to Q 10 are each independently a hydrogen atom or a substituent. In the above general formulae (TEMP-42) to (TEMP-52), * represents a bonding position.

[0085] [ka]

[0086] In the general formulae (TEMP-53) to (TEMP-62), Q1 to Q 10 are each independently a hydrogen atom or a substituent. Equations Q9 and Q 10 may be bonded to each other via a single bond to form a ring. In the above general formulae (TEMP-53) to (TEMP-62), * represents a bonding position.

[0087] [ka]

[0088] In the general formulae (TEMP-63) to (TEMP-68), Q1 to Q8 each independently represent a hydrogen atom or a substituent. In the above general formulae (TEMP-63) to (TEMP-68), * represents a bonding position.

[0089] The substituted or unsubstituted divalent heterocyclic group described in this specification is preferably any of the groups represented by the following general formulae (TEMP-69) to (TEMP-102), unless otherwise specified in this specification.

[0090] [ka]

[0091] [ka]

[0092] [ka]

[0093] In the general formulae (TEMP-69) to (TEMP-82), Q1 to Q9 each independently represent a hydrogen atom or a substituent.

[0094] [ka]

[0095] [ka]

[0096] [ka]

[0097] [ka]

[0098] In the general formulae (TEMP-83) to (TEMP-102), Q1 to Q8 each independently represent a hydrogen atom or a substituent.

[0099] The above is an explanation of "the substituents described in this specification".

[0100] - "When bonded to form a ring" In this specification, the phrase "one or more of a set consisting of two or more adjacent groups bond to each other to form a substituted or unsubstituted monocycle, bond to each other to form a substituted or unsubstituted fused ring, or are not bonded to each other" means the case where "one or more of a set consisting of two or more adjacent groups bond to each other to form a substituted or unsubstituted monocycle", the case where "one or more of a set consisting of two or more adjacent groups bond to each other to form a substituted or unsubstituted fused ring", and the case where "one or more of a set consisting of two or more adjacent groups are not bonded to each other". In this specification, the cases where "one or more of a set of two or more adjacent rings are bonded to each other to form a substituted or unsubstituted monocyclic ring" and "one or more of a set of two or more adjacent rings are bonded to each other to form a substituted or unsubstituted condensed ring" (hereinafter, these cases may be collectively referred to as "a case where they are bonded to form a ring") will be explained below. The case of an anthracene compound represented by the following general formula (TEMP-103), in which the mother skeleton is an anthracene ring, will be explained as an example.

[0101] [ka]

[0102] For example, R921 ~R 930 In the case where "one or more pairs of adjacent two or more groups are bonded to each other to form a ring," one pair of adjacent two groups is R 921 and R 922 With R 922 and R 923 With R 923 and R 924 With R 924 and R 930 With R 930 and R 925 With R 925 and R 926 With R 926 and R 927 With R 927 and R 928 With R 928 and R 929 and R 929 and R 921 It is paired with .

[0103] The above "one or more pairs" means that two or more pairs of adjacent two or more groups may simultaneously form a ring. For example, R 921 and R 922 and are bonded to ring Q A At the same time, R 925 and R 926 and are bonded to ring Q B When the above general formula (TEMP-103) is formed, the anthracene compound represented by the general formula (TEMP-104) is represented by the following general formula (TEMP-104).

[0104] [ka]

[0105] The case where a "set of two or more adjacent units" forms a ring includes not only the case where a set of two adjacent units is bonded as in the previous example, but also the case where a set of three or more adjacent units is bonded. For example, R 921 and R 922 and are bonded to ring Q A and R 922 and R923 and are bonded to ring Q C The three adjacent (R 921 , R 922 and R 923 In this case, the anthracene compound represented by the general formula (TEMP-103) is represented by the following general formula (TEMP-105). In the following general formula (TEMP-105), the ring Q A and Ring Q C is R 922 Share.

[0106] [ka]

[0107] The "monocyclic ring" or "condensed ring" formed may be a saturated or unsaturated ring as the structure of only the ring formed. Even when "one of the pairs of adjacent two" forms a "monocyclic ring" or a "condensed ring", the "monocyclic ring" or the "condensed ring" may form a saturated or unsaturated ring. For example, the ring Q formed in the general formula (TEMP-104) may be a saturated or unsaturated ring. A and Ring Q B are "monocyclic" or "condensed rings". In addition, the ring Q formed in the general formula (TEMP-105) A , and ring Q C is a "fused ring". The ring Q in the above general formula (TEMP-105) A and Kan Q C That is, Ring Q A and Kan Q C The ring Q in the general formula (TMEP-104) is condensed to form a condensed ring. A If is a benzene ring, then ring Q A The ring Q in the general formula (TMEP-104) is a monocyclic ring. A If is a naphthalene ring, then ring Q A is a fused ring.

[0108] The term "unsaturated ring" refers to an aromatic hydrocarbon ring or an aromatic heterocyclic ring. The term "saturated ring" refers to an aliphatic hydrocarbon ring or a non-aromatic heterocyclic ring. Specific examples of the aromatic hydrocarbon ring include structures in which the groups given as specific examples in the specific example group G1 are terminated with a hydrogen atom. Specific examples of the aromatic heterocycle include structures in which the aromatic heterocyclic groups exemplified as specific examples in the specific example group G2 are terminated with a hydrogen atom. Specific examples of the aliphatic hydrocarbon ring include structures in which the groups given as specific examples in the specific example group G6 are terminated with a hydrogen atom. The term "form a ring" means that a ring is formed only with a plurality of atoms of the parent skeleton, or with a plurality of atoms of the parent skeleton and one or more optional elements. For example, R 921 and R 922 and are bonded together to form a ring Q A is R 921 The carbon atom of the anthracene skeleton to which R is bonded 922 It means a ring formed by the carbon atom of the anthracene skeleton to which R is bonded and one or more arbitrary elements. 921 and R 922 Todekan Q A In the case where R 921 The carbon atom of the anthracene skeleton to which R is bonded 922 When the carbon atom of the anthracene skeleton to which R is bonded forms a monocyclic unsaturated ring with four carbon atoms, R 921 and R 922 The ring formed by this is a benzene ring.

[0109] Here, unless otherwise specified in the present specification, the "arbitrary element" is preferably at least one element selected from the group consisting of carbon, nitrogen, oxygen, and sulfur. In the arbitrary element (for example, in the case of a carbon element or a nitrogen element), a bond that does not form a ring may be terminated with a hydrogen atom or the like, or may be substituted with an "arbitrary substituent" described below. When an arbitrary element other than a carbon element is included, the ring formed is a heterocycle. Unless otherwise specified in this specification, the "one or more arbitrary elements" constituting a single ring or a condensed ring is preferably 2 or more and 15 or less, more preferably 3 or more and 12 or less, and even more preferably 3 or more and 5 or less. Unless otherwise specified in this specification, of the "monocyclic ring" and the "condensed ring", the "monocyclic ring" is preferred. Unless otherwise specified in this specification, of the "saturated ring" and the "unsaturated ring", the "unsaturated ring" is preferred. Unless otherwise specified in this specification, a "monocyclic ring" is preferably a benzene ring. Unless otherwise specified in this specification, the "unsaturated ring" is preferably a benzene ring. When "one or more of a set of two or more adjacent rings" "combine with each other to form a substituted or unsubstituted monocyclic ring" or "combine with each other to form a substituted or unsubstituted fused ring", unless otherwise specified in this specification, preferably, one or more of a set of two or more adjacent rings combine with each other to form a substituted or unsubstituted "unsaturated ring" consisting of a plurality of atoms of the parent skeleton and at least one element selected from the group consisting of 1 to 15 carbon elements, nitrogen elements, oxygen elements, and sulfur elements.

[0110] When the above-mentioned "monocyclic ring" or "condensed ring" has a substituent, the substituent is, for example, the "optional substituent" described later. When the above-mentioned "monocyclic ring" or "condensed ring" has a substituent, specific examples of the substituent are the substituents described in the above-mentioned section "Substituents described in this specification". When the above-mentioned "saturated ring" or "unsaturated ring" has a substituent, the substituent is, for example, the "optional substituent" described below. When the above-mentioned "monocyclic ring" or "condensed ring" has a substituent, specific examples of the substituent are the substituents described in the above section "Substituents described in this specification". The above is an explanation of the case where "one or more pairs of adjacent groups bond with each other to form a substituted or unsubstituted monocyclic ring" and the case where "one or more pairs of adjacent groups bond with each other to form a substituted or unsubstituted fused ring" ("combined to form a ring").

[0111] Substituents in the phrase "substituted or unsubstituted" In one embodiment of the present specification, the substituent in the case of "substituted or unsubstituted" (sometimes referred to as "optional substituent" in the present specification) is, for example, an unsubstituted alkyl group having 1 to 50 carbon atoms, an unsubstituted alkenyl group having 2 to 50 carbon atoms, an unsubstituted alkynyl group having 2 to 50 carbon atoms, an unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms; -Si(R 901 )(R 902 )(R 903 ), -O-(R 904 ), -S-(R 905 ), -N(R 906 )(R 907 ), Halogen atoms, cyano groups, nitro groups, an unsubstituted aryl group having 6 to 50 ring carbon atoms, and Unsubstituted heterocyclic group having 5 to 50 ring atoms and the like, Here, R 901 ~R 907 are each independently Hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms; a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, or It is a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms. R 901 If there are two or more, there are two or more R 901 are identical or different from each other, R 902 If there are two or more, there are two or more R 902 are identical or different from each other, R 903If there are two or more, there are two or more R 903 are identical or different from each other, R 904 If there are two or more, there are two or more R 904 are identical or different from each other, R 905 If there are two or more, there are two or more R 905 are identical or different from each other, R 906 If there are two or more, there are two or more R 906 are identical or different from each other, R 907 If there are two or more, there are two or more R 907 are the same or different from each other.

[0112] In one embodiment, the substituent in the above "substituted or unsubstituted" is: an alkyl group having 1 to 50 carbon atoms; an aryl group having 6 to 50 ring carbon atoms, and Heterocyclic groups with 5 to 50 ring atoms is a group selected from the group consisting of:

[0113] In one embodiment, the substituent in the above "substituted or unsubstituted" is: an alkyl group having 1 to 18 carbon atoms; An aryl group having 6 to 18 ring carbon atoms, and Heterocyclic groups with 5 to 18 ring atoms is a group selected from the group consisting of:

[0114] Specific examples of each group of the above optional substituents are the specific examples of the substituents described above in the section "Substituents described in this specification."

[0115] Unless otherwise specified in this specification, any adjacent substituents may be combined with each other to form a "saturated ring" or an "unsaturated ring", preferably a substituted or unsubstituted saturated 5-membered ring, a substituted or unsubstituted saturated 6-membered ring, a substituted or unsubstituted unsaturated 5-membered ring, or a substituted or unsubstituted unsaturated 6-membered ring, more preferably a benzene ring. Unless otherwise specified in the present specification, the optional substituent may further have a substituent. The substituent that the optional substituent further has is the same as the optional substituent described above.

[0116] In this specification, a numerical range expressed using "AA to BB" means a range including the number AA written before "AA to BB" as the lower limit and the number BB written after "AA to BB" as the upper limit.

[0117] The compounds of the present invention will be described below. The compound of the present invention is a compound represented by the following formula (1), and the molecular weight of the compound is not less than 650. Hereinafter, the compounds of the present invention represented by formula (1) and each formula belonging to the subgroup of formula (1) described below may be simply referred to as "invention compounds". [ka]

[0118] The molecular weight of the compound represented by formula (1) of the present invention is at least 650. If the molecular weight of the invention compound is less than 650, the glass transition temperature Tg is likely to be low, and the life of the element may be shortened from the viewpoint of heat resistance against heat generated when the element is driven (hereinafter, sometimes referred to as "driving heat"). The molecular weight of the compound of the invention is preferably 650 to 5000, more preferably 650 to 3000, and further preferably 650 to 1000. When the molecular weight is within this range, the glass transition temperature Tg can be maintained high, so that the compound of the invention becomes relatively stable against heat such as driving heat, and deterioration and deformation of film properties are suppressed, thereby improving the life of the element. The glass transition temperature of the compound of the invention is preferably 125° C. or higher, more preferably 130° C. or higher, and even more preferably 140° C. or higher.

[0119] The symbols in the above formulae and in the formulae described below will be explained below. Unless otherwise specified, the same symbols have the same meaning.

[0120] Y 1 and Y 2 One of the is a nitrogen atom and the other is CR. That is, Y 1 is nitrogen atom and Y 2 CR or Y 1 CR and Y 2 is a nitrogen atom. n is an integer of 1 to 3, and when n is an integer of 2 or 3, the two or three Cz's are the same or different from each other.

[0121] R is selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a fluorine atom, and a cyano group, and is preferably selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, and a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, and is more preferably a hydrogen atom.

[0122] The details of the substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms are as described in “Substituents described in this specification”, and more preferably, the substituted or unsubstituted aryl group is a phenyl group, a p-biphenyl group, a m-biphenyl group, an o-biphenyl group, a p-terphenyl-4-yl group, a p-terphenyl-3-yl group, a p-terphenyl-2-yl group, a m-terphenyl-4-yl group, a m-terphenyl-3-yl group, a m-terphenyl-2-yl group, an o-terphenyl-4-yl group, an o-terphenyl-3 ... Preferred examples thereof include a phenyl group, an o-terphenyl-2-yl group, a 1-naphthyl group, a 2-naphthyl group, a fluorenyl group, a 9,9'-spirobifluorenyl group, a 9,9-dimethylfluorenyl group, and a 9,9-diphenylfluorenyl group, and more preferred examples thereof include a phenyl group, a p-biphenyl group, an m-biphenyl group, an o-biphenyl group, a 1-naphthyl group, a 2-naphthyl group, a fluorenyl group, a 9,9'-spirobifluorenyl group, a 9,9-dimethylfluorenyl group, and a 9,9-diphenylfluorenyl group.

[0123] The details of the substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms are as described in “Substituents Described in the Present Description”, and are more preferably a carbazolyl group (a 1-carbazolyl group, a 2-carbazolyl group, a 3-carbazolyl group, a 4-carbazolyl group, or a 9-carbazolyl group), a dibenzofuranyl group, a naphthobenzofuranyl group, a dibenzothiophenyl group, a naphthobenzothiophenyl group, a phenyldibenzofuranyl group, or a phenyldibenzothiophenyl group, and are further preferably a carbazolyl group (a 1-carbazolyl group, a 2-carbazolyl group, a 3-carbazolyl group, a 4-carbazolyl group, or a 9-carbazolyl group), a dibenzofuranyl group, or a dibenzothiophenyl group.

[0124] Details of the substituted or unsubstituted alkyl group having 1 to 50 carbon atoms are as described in “Substituents described in this specification”, and is preferably a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, an s-butyl group, or a t-butyl group, and more preferably a methyl group, an isopropyl group, or a t-butyl group.

[0125] The details of the substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms are as described in “Substituents described in this specification”, and are preferably a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, or a cyclohexyl group, and more preferably a cyclopropyl group, a cyclopentyl group, or a cyclohexyl group.

[0126] R 1 ~R 6 are each independently selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a fluorine atom, and a cyano group, and are preferably selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, and a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, and are more preferably a hydrogen atom. R 1 ~R 6 Adjacent two selected from the following do not bond to each other to form a ring.

[0127] Details of the substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, the substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, the substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, and the substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms are the same as the details of the corresponding groups described above for R.

[0128] L 3 and L 4 are each independently selected from a single bond or a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms. However, when n is an integer of 2 or 3, L 4 represents a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms.

[0129] L 3 and L 4As one embodiment of the present invention, L 3 and L 4 are each preferably independently a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms. In another embodiment, L 3 is a single bond and L 4 is a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms, or L 3 and L 4 is preferably a single bond.

[0130] Details of the substituted or unsubstituted arylene group having 6 to 50 carbon atoms are as described in “Substituents Described in This Specification”, and examples thereof include a divalent group derived by removing one hydrogen atom on the aryl ring from the above-mentioned “substituted or unsubstituted aryl group having 6 to 50 carbon atoms”. L 3 and L 4 The unsubstituted arylene groups of the substituted or unsubstituted arylene groups having 6 to 50 ring carbon atoms represented by the formula (I) are preferably each independently selected from a phenylene group, a biphenylene group, a naphthylene group, a phenanthrylene group, and an anthracenylene group.

[0131] Ar 1 and Ar 2 are each independently selected from a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms and a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms.

[0132] Details of the substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms are the same as those of the corresponding group described above for R. Ar 1 and Ar 2 It is preferable that the unsubstituted aryl groups of the substituted or unsubstituted aryl groups having 6 to 50 ring carbon atoms represented by the formula (I) are each independently selected from a phenyl group, a biphenyl group, a naphthyl group, a phenanthryl group, an anthracenyl group, a chrysenyl group and a pyrenyl group.

[0133] Details of the substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms are the same as those of the corresponding groups described above for R. Ar 1 and Ar 2 It is preferable that the unsubstituted heterocyclic groups of the substituted or unsubstituted heterocyclic groups having 5 to 50 ring atoms represented by the formula (I) are each independently selected from a pyridyl group, a dibenzothiophenyl group, a dibenzofuranyl group, an azadibenzofuranyl group, a pyrimidinyl group, a quinolyl group, an isoquinolyl group, a benzothiophenyl group, and a benzofuranyl group.

[0134] L 1 and L 2 are each independently selected from a single bond or a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms. L 1 and L 2 As one embodiment of the present invention, L 1 and L 2 It is preferable that one of them is a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms, and the remaining one is a single bond. L 1 and L 2 As another embodiment of the present invention, L 1 and L 2 are each preferably independently a substituted or unsubstituted arylene group having 6 to 50 ring carbon atoms. In yet another embodiment, L 1 and L 2 is preferably a single bond.

[0135] The details of the substituted or unsubstituted arylene group having 6 to 50 carbon atoms are as follows: 3 and L 4 The details of the arylene group are the same as those described above with respect to L 1 and L 2 It is preferable that the unsubstituted arylene groups of the substituted or unsubstituted arylene groups having 6 to 50 ring carbon atoms represented by the formula (I) are each independently selected from a phenylene group, a biphenylene group, a naphthylene group, a phenanthrylene group, a fluorenylene group, and an anthracenylene group.

[0136] Cz is a group represented by the following formula (1-a) or formula (1-b). [ka]

[0137] R 21 ~R 28 and R 31 ~R 38 are each independently a hydrogen atom or a substituent. The substituent is selected from a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms and not having a nitrogen-containing 5-membered ring or a nitrogen-containing 7-membered ring, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms, a fluorine atom, and a cyano group. It is preferably selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms and not having a nitrogen-containing 5-membered ring or a nitrogen-containing 7-membered ring, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, and a cyano group, and is more preferably a hydrogen atom. However, R 21 ~R 28 Two adjacent ones selected from R 31 ~R 38 Two adjacent ones selected from R 24 and R 25 and R 34 and R 35 do not bond to each other to form a ring. Also, R 21 ~R 28 One selected from *a through L 3 b is a single bond that bonds to L 3 represents the position at which the molecule binds to the molecule.

[0138] Details of the substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, the substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, and the substituted or unsubstituted cycloalkyl group having 3 to 50 ring carbon atoms are the same as the details of the corresponding groups described above for R, respectively. In addition, details of the substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms and not having a nitrogen-containing 5-membered ring or a nitrogen-containing 7-membered ring are the same as those of the heterocyclic group described above for R, excluding the heterocyclic groups having a nitrogen-containing 5-membered ring and a nitrogen-containing 7-membered ring.

[0139] In one embodiment of the present invention, L 3 R that is not a single bond 21 ~R 28 At least one selected from, or R 31 ~R 38 It is preferable that at least one selected from the group consisting of: *L via a 3 R that is not a single bond 21 ~R 28 and R 31 ~R 38 is preferably selected from a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms and a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms. *L via a 3 R that is not a single bond 21 ~R 28 and R 31 ~R 38 In the substituent represented by the formula (I), at least one of the unsubstituted substituents is preferably selected from a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a s-butyl group, a t-butyl group, a phenyl group, a biphenyl group, a naphthyl group, a phenanthryl group, and a cyano group.

[0140] R a is selected from a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms and a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms.

[0141] Details of the substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms and the substituted or unsubstituted alkyl group having 1 to 50 carbon atoms are the same as those of the corresponding groups described above for R, respectively. R a The unsubstituted aryl group of the substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms represented by the formula (I) is preferably selected from a phenyl group, a biphenyl group, a naphthyl group, and a phenanthryl group. R a The unsubstituted alkyl group in the substituted or unsubstituted alkyl group having 1 to 50 ring carbon atoms represented by is preferably selected from a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, an s-butyl group, and a t-butyl group.

[0142] In a preferred embodiment of the present invention, the compounds of the invention include compounds represented by formula (1-b-1) or (1-b-2). [ka]

[0143] Y 1 , Y 2 , Ar 1 , Ar 2 , L 1 , L 2 , R 1 ~R 6 and R 31 ~R 38 is as defined above, and R 41 ~R 42 , R 44 ~R 45 , R 51 ~R 52 and R 54 ~R 55 are each independently selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, and a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms.

[0144] R 41 ~R 42 , R 44 ~R 45 , R51 ~R 52 and R 54 ~R 55 Details of the substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms and the substituted or unsubstituted alkyl group having 1 to 50 carbon atoms represented by are the same as those of the corresponding groups described above for R.

[0145] R 41 ~R 42 , R 44 ~R 45 , R 51 ~R 52 and R 54 ~R 55 At least one pair of adjacent two selected from, i.e., R 41 and R 42 , R 44 and R 45 , R 51 and R 52 , and R 54 and R 55 At least one pair of adjacent two selected from the group consisting of may be bonded to each other independently to form a substituted or unsubstituted benzene ring, or may not be bonded to each other and therefore not form the benzene ring. In one aspect of the present invention, it is preferable that the benzene ring is not formed. In another aspect of the present invention, it is preferable that the benzene ring is formed.

[0146] In a preferred embodiment of the present invention, the compound of the present invention includes a compound represented by any one of formulas (1-b-11) to (1-b-14). [ka]

[0147] Y 1 , Y 2 , Ar 1 , Ar 2 , L 1 , L 2 , R 1 ~R 6 , R 31 ~R 38 , R 41 and R 44 ~R45 are as defined above. 43 is selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, and a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms.

[0148] R 43 Details of the substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms and the substituted or unsubstituted alkyl group having 1 to 50 carbon atoms represented by are the same as those of the corresponding groups described above for R.

[0149] In a preferred embodiment of the present invention, the compound of the present invention includes a compound represented by any one of formulas (1-a-1) to (1-a-4). [ka]

[0150] Y 1 , Y 2 , Ar 1 , Ar 2 , L 1 , L 2 , R a , R 1 ~R 6 , R 21 ~R 28 , R 41 ~R 42 and R 44 ~R 45 is as defined above.

[0151] In one aspect of the present invention, (1)R 1 ~R 6 may all be hydrogen atoms, (2)R 41 ~R 45 may all be hydrogen atoms, (3)R 51 ~R 52 and R 54 ~R 55 may all be hydrogen atoms, (4)*a through L 3R that is not a single bond 21 ~R 28 All of the substituents other than the one selected from the group may be hydrogen atoms, (5)R 31 ~R 38 All of the substituents other than the substituent selected from may be hydrogen atoms. The compounds of the invention may simultaneously satisfy two or more of the above conditions (1) to (5) depending on their configuration.

[0152] As noted above, the term "hydrogen atom" as used herein includes protium, deuterium, and tritium atoms. Thus, the compounds of the invention may contain naturally occurring deuterium atoms. Alternatively, a deuterium atom may be intentionally introduced into the compound of the invention by using a compound in which some or all of the raw material compounds are deuterated. Thus, in one embodiment of the present invention, the compound of the invention contains at least one deuterium atom. That is, the compound of the invention may be a compound represented by formula (1) or a formula included in formula (1), in which at least one of the hydrogen atoms contained in the compound is a deuterium atom. In formula (1), R, R 1 ~R 6 , *R that is not a single bond bonded to a 21 ~R 28 , R 31 ~R 38 , R 41 ~R 45 , R 51 ~R 52 and R 54 ~R 55 Hydrogen atoms represented by R and R 1 ~R 6 , *R that is not a single bond bonded to a 21 ~R 28 , R 31 ~R 38 , R 41 ~R 45 , R 51 ~R 52 and R 54 ~R 55 A hydrogen atom of the substituent represented by 1 , L 2 , L 3and L 4 A hydrogen atom possessed by the arylene group represented by R a At least one hydrogen atom selected from the hydrogen atoms of the aryl group represented by Ar 1 and Ar 2 At least one hydrogen atom selected from the hydrogen atoms contained in the aryl group or heterocyclic group represented by the formula (I) may be a deuterium atom.

[0153] The deuteration rate of the invention compound (the ratio of the number of deuterium atoms to the total number of hydrogen atoms in the invention compound) depends on the deuteration rate of the raw material compounds used. Since it is usually difficult to make the deuteration rate of all raw material compounds used 100%, the deuteration rate of the invention compound is less than 100%. The deuteration rate of the compound of the invention is 1% or more, preferably 3% or more, more preferably 5% or more, and further preferably 10% or more.

[0154] The invention compound may be a mixture containing a deuterated compound (a compound into which a deuterium atom has been intentionally introduced) and a non-deuterated compound, or a mixture of two or more compounds having different deuteration rates. The deuteration rate of such a mixture (the ratio of the number of deuterium atoms to the total number of hydrogen atoms in the invention compound contained in the mixture) is 1% or more, preferably 3% or more, more preferably 5% or more, and even more preferably 10% or more, and less than 100%.

[0155] In the compound of the invention, at least one hydrogen atom selected from the hydrogen atom represented by R or the hydrogen atoms possessed by the substituent represented by R may be a deuterium atom. The deuteration rate (the ratio of the number of deuterium atoms to the total number of hydrogen atoms possessed by the hydrogen atom represented by R or the substituent represented by R) is 1% or more, preferably 3% or more, more preferably 5% or more, and even more preferably 10% or more, and less than 100%.

[0156] In the invention compound, R 1 ~R 6 or R 1 ~R 6At least one hydrogen atom selected from the hydrogen atoms of the substituent represented by may be a deuterium atom. 1 ~R 6 or R 1 ~R 6 The ratio of the number of deuterium atoms to the total number of hydrogen atoms of the substituent represented by (a) is 1% or more, preferably 3% or more, more preferably 5% or more, and further preferably 10% or more and less than 100%.

[0157] In the compound of the invention, R that is not a single bond bonded to *a 21 ~R 28 A hydrogen atom represented by or a R that is not a single bond bonded to *a 21 ~R 28 At least one hydrogen atom selected from the hydrogen atoms of the substituent represented by may be a deuterium atom. 21 ~R 28 A hydrogen atom represented by or a R that is not a single bond bonded to *a 21 ~R 28 The ratio of the number of deuterium atoms to the total number of hydrogen atoms of the substituent represented by (a) is 1% or more, preferably 3% or more, more preferably 5% or more, and further preferably 10% or more and less than 100%.

[0158] In the invention compound, R 31 ~R 38 or R 31 ~R 38 At least one hydrogen atom selected from the hydrogen atoms of the substituent represented by may be a deuterium atom. 31 ~R 38 or R 31 ~R 38 The ratio of the number of deuterium atoms to the total number of hydrogen atoms of the substituent represented by (a) is 1% or more, preferably 3% or more, more preferably 5% or more, and further preferably 10% or more and less than 100%.

[0159] In the invention compound, L 1 and L 2At least one hydrogen atom selected from the hydrogen atoms of the arylene group represented by the formula (I) may be a deuterium atom. 1 and L 2 The ratio of the number of deuterium atoms to the total number of hydrogen atoms in the arylene group represented by (a) is 1% or more, preferably 3% or more, more preferably 5% or more, and further preferably 10% or more and less than 100%.

[0160] In the invention compound, L 3 and L 4 At least one hydrogen atom selected from the hydrogen atoms of the arylene group represented by the formula (I) may be a deuterium atom. 3 and L 4 The ratio of the number of deuterium atoms to the total number of hydrogen atoms in the arylene group represented by (a) is 1% or more, preferably 3% or more, more preferably 5% or more, and further preferably 10% or more and less than 100%.

[0161] In the invention compound, R a At least one hydrogen atom selected from the hydrogen atoms of the aryl group represented by may be a deuterium atom. a The ratio of the number of deuterium atoms to the total number of hydrogen atoms in the aryl group represented by (a) is 1% or more, preferably 3% or more, more preferably 5% or more, and further preferably 10% or more and less than 100%.

[0162] In the invention compound, Ar 1 and Ar 2 At least one hydrogen atom selected from the hydrogen atoms of the aryl group or heterocyclic group represented by the formula (I) may be a deuterium atom. 1 and Ar 2 The ratio of the number of deuterium atoms to the total number of hydrogen atoms in the aryl group or heterocyclic group represented by the formula (I) is 1% or more, preferably 3% or more, more preferably 5% or more, and further preferably 10% or more and less than 100%.

[0163] Details of the substituents (optional substituents) in the case of "substituted or unsubstituted" included in the definition of each formula above are as described in "Substituents in the case of "substituted or unsubstituted".

[0164] Those skilled in the art can easily prepare the compounds of the invention by referring to the synthesis examples below and known synthesis methods.

[0165] Specific examples of the compound of the invention are shown below, but the invention is not limited to these exemplary compounds. In the following specific examples, D represents a deuterium atom.

[0166] [ka]

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[0189] Materials for organic electroluminescence devices The material for organic EL devices of the present invention contains the compound of the present invention. The content of the compound of the present invention in the material for organic EL devices is 1% by mass or more (including 100%), preferably 10% by mass or more (including 100%), more preferably 50% by mass or more (including 100%), even more preferably 80% by mass or more (including 100%), even more preferably 90% by mass or more (including 100%), even more preferably 95% by mass or more (including 100%), particularly preferably 99% by mass or more (including 100%), and most preferably 99.9% by mass or more (including 100%). The material for organic EL devices of the present invention is useful for the production of organic EL devices.

[0190] Organic EL element The organic EL device of the present invention comprises an anode, a cathode, and an organic layer disposed between the anode and the cathode, the organic layer including a light-emitting layer, and at least one of the organic layers includes a compound of the present invention. Examples of the organic layer containing the compound of the invention include, but are not limited to, a hole transport zone (hole injection layer, hole transport layer, electron blocking layer, exciton blocking layer, etc.) provided between the anode and the light emitting layer, the light emitting layer, a spacer layer, an electron transport zone (electron injection layer, electron transport layer, hole blocking layer, etc.) provided between the cathode and the light emitting layer, etc. The compound of the invention is preferably a material for the electron transport zone or light emitting layer of a fluorescent or phosphorescent EL device, more preferably a material for the electron transport zone, even more preferably a material for the electron injection layer, electron transport layer, or hole blocking layer, and particularly preferably a material for the hole blocking layer.

[0191] The organic EL device of the present invention may be a monochromatic light-emitting device of a fluorescent or phosphorescent type, a white light-emitting device of a fluorescent / phosphorescent hybrid type, a simple type having a single light-emitting unit, or a tandem type having multiple light-emitting units, and is preferably a fluorescent type device. Here, the term "light-emitting unit" refers to a minimum unit that includes an organic layer, at least one of which is a light-emitting layer, and emits light by recombination of injected holes and electrons.

[0192] For example, the following device configuration can be given as a representative device configuration of a simple type organic EL device. (1) Anode / light-emitting unit / cathode The light-emitting unit may be a multi-layer type having a plurality of phosphorescent or fluorescent light-emitting layers, in which case a spacer layer may be provided between each light-emitting layer to prevent excitons generated in the phosphorescent light-emitting layer from diffusing to the fluorescent light-emitting layer. A typical layer structure of a simple light-emitting unit is shown below. The layers in parentheses are optional. (a) (hole injection layer / ) hole transport layer / fluorescent light-emitting layer / electron transport layer ( / electron injection layer) (b) (hole injection layer / ) hole transport layer / phosphorescent light-emitting layer electron transport layer ( / electron injection layer) (c) (hole injection layer / ) hole transport layer / first fluorescent-emitting layer / second fluorescent-emitting layer / electron transport layer ( / electron injection layer) (d) (hole injection layer / ) hole transport layer / first phosphorescent emitting layer / second phosphorescent emitting layer / electron transport layer ( / electron injection layer) (e) (hole injection layer / ) hole transport layer / phosphorescent emitting layer / space layer / fluorescent emitting layer / electron transport layer ( / electron injection layer) (f) (hole injection layer / ) hole transport layer / first phosphorescent emitting layer / second phosphorescent emitting layer / space layer / fluorescent emitting layer / electron transport layer ( / electron injection layer) (g) (hole injection layer / ) hole transport layer / first phosphorescent emitting layer / space layer / second phosphorescent emitting layer / space layer / fluorescent emitting layer / electron transport layer ( / electron injection layer) (h) (hole injection layer / ) hole transport layer / phosphorescent emitting layer / space layer / first fluorescent emitting layer / second fluorescent emitting layer / electron transport layer ( / electron injection layer) (i) (hole injection layer / ) hole transport layer / electron blocking layer / fluorescent emitting layer / electron transport layer ( / electron injection layer) (j) (hole injection layer / ) hole transport layer / electron blocking layer / phosphorescent emitting layer / electron transport layer ( / electron injection layer) (k) (hole injection layer / ) hole transport layer / exciton blocking layer / fluorescent emitting layer / electron transport layer ( / electron injection layer) (l) (hole injection layer / ) hole transport layer / exciton blocking layer / phosphorescent emitting layer / electron transport layer ( / electron injection layer) (m) (hole injection layer / ) first hole transport layer / second hole transport layer / fluorescent light-emitting layer / electron transport layer ( / electron injection layer) (n) (hole injection layer / ) first hole transport layer / second hole transport layer / phosphorescent emitting layer / electron transport layer ( / electron injection layer) (o) (hole injection layer / ) first hole transport layer / second hole transport layer / fluorescent light-emitting layer / first electron transport layer / second electron transport layer ( / electron injection layer) (p) (hole injection layer / ) first hole transport layer / second hole transport layer / phosphorescent emitting layer / first electron transport layer / second electron transport layer ( / electron injection layer) (q) (hole injection layer / ) hole transport layer / fluorescent light-emitting layer / hole blocking layer / electron transport layer ( / electron injection layer) (r) (hole injection layer / ) hole transport layer / phosphorescent emitting layer / hole blocking layer / electron transport layer ( / electron injection layer) (s) (hole injection layer / ) hole transport layer / fluorescent emitting layer / exciton blocking layer / electron transport layer ( / electron injection layer) (t) (hole injection layer / ) hole transport layer / phosphorescent emitting layer / exciton blocking layer / electron transport layer ( / electron injection layer)

[0193] The phosphorescent or fluorescent emitting layers may each emit light of a different color. Specifically, the light emitting unit (f) may have a layer structure such as (hole injection layer / ) hole transport layer / first phosphorescent emitting layer (red light emission) / second phosphorescent emitting layer (green light emission) / space layer / fluorescent emitting layer (blue light emission) / electron transport layer. An electron blocking layer may be provided between each light-emitting layer and the hole transport layer or between each spacer layer as needed. Also, a hole blocking layer may be provided between each light-emitting layer and the electron transport layer as needed. By providing an electron blocking layer or a hole blocking layer, electrons or holes can be confined within the light-emitting layer, increasing the probability of charge recombination in the light-emitting layer and improving the light-emitting efficiency.

[0194] Representative device configurations of tandem-type organic EL devices include the following. (2) Anode / first light-emitting unit / intermediate layer / second light-emitting unit / cathode Here, the first light-emitting unit and the second light-emitting unit can be, for example, independently selected from the light-emitting units described above. The intermediate layer is generally also called an intermediate electrode, intermediate conductive layer, charge generating layer, electron extracting layer, connecting layer, or intermediate insulating layer, and can be made of a known material configuration that supplies electrons to the first light-emitting unit and holes to the second light-emitting unit.

[0195] FIG. 1 is a schematic diagram showing an example of the configuration of an organic EL device of the present invention. The organic EL device 1 has a substrate 2, an anode 3, a cathode 4, and an emitting unit 10 disposed between the anode 3 and the cathode 4. The emitting unit 10 has an emitting layer 5. A hole transport zone 6 (hole injection layer, hole transport layer, etc.) is provided between the emitting layer 5 and the anode 3, and an electron transport zone 7 (electron injection layer, electron transport layer, etc.) is provided between the emitting layer 5 and the cathode 4. In addition, an electron blocking layer (not shown) may be provided on the anode 3 side of the emitting layer 5, and a hole blocking layer (not shown) may be provided on the cathode 4 side of the emitting layer 5. This allows electrons and holes to be trapped in the emitting layer 5, thereby further increasing the efficiency of generating excitons in the emitting layer 5.

[0196] 2 is a schematic diagram showing another configuration of the organic EL element of the present invention. The organic EL element 11 has a substrate 2, an anode 3, a cathode 4, and an emitting unit 20 disposed between the anode 3 and the cathode 4. The emitting unit 20 has an emitting layer 5. The emitting unit 20 also has a hole transport zone 6 (hole injection layer, hole transport layer, etc.) disposed between the anode 3 and the emitting layer 5. The emitting unit 20 further has an electron transport zone disposed between the emitting layer 5 and the cathode 4, and the electron transport zone is formed of a hole blocking layer 7a, an electron transport layer 7b, and an electron injection layer 7c.

[0197] In the present invention, a host combined with a fluorescent dopant (fluorescent light-emitting material) is called a fluorescent host, and a host combined with a phosphorescent dopant is called a phosphorescent host. The fluorescent host and the phosphorescent host are not distinguished only by their molecular structures. That is, the phosphorescent host means a material that forms a phosphorescent light-emitting layer containing a phosphorescent dopant, and does not mean that it cannot be used as a material that forms a fluorescent light-emitting layer. The same applies to the fluorescent host.

[0198] substrate The substrate is used as a support for the organic EL element. For example, a plate such as glass, quartz, or plastic can be used as the substrate. A flexible substrate can also be used. For example, a plastic substrate made of polycarbonate, polyarylate, polyethersulfone, polypropylene, polyester, polyvinyl fluoride, or polyvinyl chloride can be used as the flexible substrate. An inorganic deposition film can also be used.

[0199] anode For the anode formed on the substrate, it is preferable to use a metal, alloy, electrically conductive compound, or a mixture thereof having a large work function (specifically, 4.0 eV or more). Specific examples include indium oxide-tin oxide (ITO), indium oxide-tin oxide containing silicon or silicon oxide, indium oxide-zinc oxide, indium oxide containing tungsten oxide and zinc oxide, graphene, etc. Other examples include gold (Au), platinum (Pt), nickel (Ni), tungsten (W), chromium (Cr), molybdenum (Mo), iron (Fe), cobalt (Co), copper (Cu), palladium (Pd), titanium (Ti), or nitrides of the above metals (e.g., titanium nitride), etc.

[0200] These materials are usually formed into a film by a sputtering method. For example, indium oxide-zinc oxide can be formed by a sputtering method using a target in which 1 to 10 wt% of zinc oxide is added to indium oxide, and indium oxide containing tungsten oxide and zinc oxide can be formed by a sputtering method using a target in which 0.5 to 5 wt% of tungsten oxide and 0.1 to 1 wt% of zinc oxide are added to indium oxide. In addition, the film may be formed by a vacuum deposition method, a coating method, an inkjet method, a spin coating method, or the like.

[0201] The hole injection layer formed in contact with the anode is formed using a material that easily injects holes regardless of the work function of the anode, and therefore materials that are commonly used as electrode materials (e.g., metals, alloys, electrically conductive compounds, and mixtures thereof, and elements belonging to Group 1 or Group 2 of the periodic table) can be used. Materials with small work functions, such as elements belonging to Group 1 or 2 of the periodic table, i.e., alkali metals such as lithium (Li) and cesium (Cs), alkaline earth metals such as magnesium (Mg), calcium (Ca), and strontium (Sr), and alloys containing these (e.g., MgAg, AlLi), rare earth metals such as europium (Eu), ytterbium (Yb), and alloys containing these, can also be used. When alkali metals, alkaline earth metals, and alloys containing these are used to form the anode, vacuum deposition and sputtering methods can be used. Furthermore, when silver paste or the like is used, coating and inkjet methods can be used.

[0202] Hole injection layer The hole injection layer is a layer containing a material with high hole injection properties (hole injection material) and is formed between the anode and the light emitting layer, or, if present, between the hole transport layer and the anode.

[0203] As the hole injecting material, molybdenum oxide, titanium oxide, vanadium oxide, rhenium oxide, ruthenium oxide, chromium oxide, zirconium oxide, hafnium oxide, tantalum oxide, silver oxide, tungsten oxide, manganese oxide, or the like can be used.

[0204] The small organic compounds 4,4',4''-tris(N,N-diphenylamino)triphenylamine (abbreviation: TDATA), 4,4',4''-tris[N-(3-methylphenyl)-N-phenylamino]triphenylamine (abbreviation: MTDATA), 4,4'-bis[N-(4-diphenylaminophenyl)-N-phenylamino]biphenyl (abbreviation: DPAB), 4,4'-bis(N-{4-[N'-(3-methylphenyl)-N'-phenylamino]phenyl}-N-phenylamino)biphenyl (abbreviation: DNTPD), 1,3,5-tris[N-(4-diphenylaminophenyl)-N-phenylamino]biphenyl (abbreviation: DNTPD), Examples of the hole injection layer material include aromatic amine compounds such as 3-[N-(9-phenylcarbazol-3-yl)-N-phenylamino]benzene (abbreviation: DPA3B), 3-[N-(9-phenylcarbazol-3-yl)-N-phenylamino]-9-phenylcarbazole (abbreviation: PCzPCA1), 3,6-bis[N-(9-phenylcarbazol-3-yl)-N-phenylamino]-9-phenylcarbazole (abbreviation: PCzPCA2), and 3-[N-(1-naphthyl)-N-(9-phenylcarbazol-3-yl)amino]-9-phenylcarbazole (abbreviation: PCzPCN1).

[0205] Polymer compounds (oligomers, dendrimers, polymers, etc.) can also be used. For example, polymer compounds such as poly(N-vinylcarbazole) (abbreviation: PVK), poly(4-vinyltriphenylamine) (abbreviation: PVTPA), poly[N-(4-{N'-[4-(4-diphenylamino)phenyl]phenyl-N'-phenylamino}phenyl)methacrylamide] (abbreviation: PTPDMA), poly[N,N'-bis(4-butylphenyl)-N,N'-bis(phenyl)benzidine] (abbreviation: Poly-TPD) can be used. In addition, polymer compounds to which an acid has been added, such as poly(3,4-ethylenedioxythiophene) / poly(styrenesulfonic acid) (PEDOT / PSS) and polyaniline / poly(styrenesulfonic acid) (PAni / PSS), can also be used.

[0206] Furthermore, it is also preferable to use an acceptor material such as a hexaazatriphenylene (HAT) compound represented by the following formula (K). [ka]

[0207] (In the above formula, R 21 ~R 26 each independently represents a cyano group, -CONH2, a carboxyl group, or -COOR 27 (R 27 represents an alkyl group having 1 to 20 carbon atoms or a cycloalkyl group having 3 to 20 carbon atoms. 21 and R 22 , R 23 and R 24 , and R 25 and R 26 adjacent two selected from may be bonded to each other to form a group represented by -CO-O-CO-.) R 27 Examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a t-butyl group, a cyclopentyl group, and a cyclohexyl group.

[0208] Hole transport layer The hole transport layer is a layer containing a material with high hole transporting properties (hole transport material), and is formed between the anode and the light emitting layer, or, if present, between the hole injection layer and the light emitting layer.

[0209] The hole transport layer may be a single-layer structure or a multi-layer structure including two or more layers. For example, the hole transport layer may be a two-layer structure including a first hole transport layer (anode side) and a second hole transport layer (cathode side). In one embodiment of the present invention, the hole transport layer of the single-layer structure is preferably adjacent to the light-emitting layer, and the hole transport layer closest to the cathode in the multi-layer structure, for example, the second hole transport layer of the two-layer structure, is preferably adjacent to the light-emitting layer. In another embodiment of the present invention, an electron blocking layer, which will be described later, may be interposed between the hole transport layer of the single-layer structure and the light-emitting layer, or between the hole transport layer closest to the light-emitting layer in the multi-layer structure and the light-emitting layer.

[0210] As the material for the hole transport layer, for example, an aromatic amine compound, a carbazole derivative, an anthracene derivative, or the like can be used. Examples of aromatic amine compounds include 4,4'-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (abbreviation: NPB), N,N'-bis(3-methylphenyl)-N,N'-diphenyl-[1,1'-biphenyl]-4,4'-diamine (abbreviation: TPD), 4-phenyl-4'-(9-phenylfluoren-9-yl)triphenylamine (abbreviation: BAFLP), 4,4'-bis[N-(9,9-dimethylfluoren-2-yl] )-N-phenylamino]biphenyl (abbreviation: DFLDPBi), 4,4',4"-tris(N,N-diphenylamino)triphenylamine (abbreviation: TDATA), 4,4',4"-tris[N-(3-methylphenyl)-N-phenylamino]triphenylamine (abbreviation: MTDATA), and 4,4'-bis[N-(spiro-9,9'-bifluoren-2-yl)-N-phenylamino]biphenyl (abbreviation: BSPB). The above compounds are -6 cm 2 / Vs or higher.

[0211] Examples of carbazole derivatives include 4,4'-di(9-carbazolyl)biphenyl (abbreviation: CBP), 9-[4-(9-carbazolyl)phenyl]-10-phenylanthracene (abbreviation: CzPA), and 9-phenyl-3-[4-(10-phenyl-9-anthryl)phenyl]-9H-carbazole (abbreviation: PCzPA). Examples of anthracene derivatives include 2-t-butyl-9,10-di(2-naphthyl)anthracene (abbreviation: t-BuDNA), 9,10-di(2-naphthyl)anthracene (abbreviation: DNA), and 9,10-diphenylanthracene (abbreviation: DPAnth). Polymer compounds such as poly(N-vinylcarbazole) (abbreviation: PVK) and poly(4-vinyltriphenylamine) (abbreviation: PVTPA) can also be used. However, compounds other than those mentioned above may be used as long as they have a higher hole transporting property than an electron transporting property.

[0212] Dopant materials for the light-emitting layer The light-emitting layer is a layer containing a highly light-emitting material (dopant material), and various materials can be used. For example, fluorescent materials and phosphorescent materials can be used as dopant materials. Fluorescent materials are compounds that emit light from a singlet excited state, and phosphorescent materials are compounds that emit light from a triplet excited state.

[0213] Examples of blue fluorescent materials that can be used in the light-emitting layer include pyrene derivatives, styrylamine derivatives, chrysene derivatives, fluoranthene derivatives, fluorene derivatives, diamine derivatives, triarylamine derivatives, etc. Specific examples include N,N'-bis[4-(9H-carbazol-9-yl)phenyl]-N,N'-diphenylstilbene-4,4'-diamine (abbreviation: YGA2S), 4-(9H-carbazol-9-yl)-4'-(10-phenyl-9-anthryl)triphenylamine (abbreviation: YGAPA), 4-(10-phenyl-9-anthryl)-4'-(9-phenyl-9H-carbazol-3-yl)triphenylamine (abbreviation: PCBAPA), etc.

[0214] As a green fluorescent material that can be used in the light-emitting layer, aromatic amine derivatives and the like can be used. Specifically, N-(9,10-diphenyl-2-anthryl)-N,9-diphenyl-9H-carbazol-3-amine (abbreviation: 2PCAPA), N-[9,10-bis(1,1'-biphenyl-2-yl)-2-anthryl]-N,9-diphenyl-9H-carbazol-3-amine (abbreviation: 2PCABPhA), N-(9,10-diphenyl-2-anthryl)-N,N',N'-triphenyl-1,4-phenylenediamine (abbreviation: 2DPAPA), N-[ 9,10-bis(1,1'-biphenyl-2-yl)-2-anthryl]-N,N',N'-triphenyl-1,4-phenylenediamine (abbreviation: 2DPABPhA), N-[9,10-bis(1,1'-biphenyl-2-yl)]-N-[4-(9H-carbazol-9-yl)phenyl]-N-phenylanthracen-2-amine (abbreviation: 2YGABPhA), N,N,9-triphenylanthracen-9-amine (abbreviation: DPhAPhA), etc.

[0215] Red fluorescent materials that can be used in the light-emitting layer include tetracene derivatives, diamine derivatives, etc. Specific examples include N,N,N',N'-tetrakis(4-methylphenyl)tetracene-5,11-diamine (abbreviation: p-mPhTD), 7,14-diphenyl-N,N,N',N'-tetrakis(4-methylphenyl)acenaphtho[1,2-a]fluoranthene-3,10-diamine (abbreviation: p-mPhAFD), etc.

[0216] As blue phosphorescent materials that can be used in the light-emitting layer, metal complexes such as iridium complexes, osmium complexes, and platinum complexes are used.Specific examples include bis[2-(4',6'-difluorophenyl)pyridinato-N,C2']iridium(III) tetrakis(1-pyrazolyl)borate (abbreviation: FIr6), bis[2-(4',6'-difluorophenyl)pyridinato-N,C2']iridium(III) picolinate (abbreviation: FIrpic), bis[2-(3',5'bistrifluoromethylphenyl)pyridinato-N,C2']iridium(III) picolinate (abbreviation: Ir(CF3ppy)2(pic)), and bis[2-(4',6'-difluorophenyl)pyridinato-N,C2']iridium(III) acetylacetonate (abbreviation: FIracac).

[0217] Iridium complexes are used as green phosphorescent materials that can be used in the light-emitting layer, including tris(2-phenylpyridinato-N,C2')iridium(III) (abbreviation: Ir(ppy)3), bis(2-phenylpyridinato-N,C2')iridium(III) acetylacetonate (abbreviation: Ir(ppy)2(acac)), bis(1,2-diphenyl-1H-benzimidazolato)iridium(III) acetylacetonate (abbreviation: Ir(pbi)2(acac)), and bis(benzo[h]quinolinato)iridium(III) acetylacetonate (abbreviation: Ir(bzq)2(acac)).

[0218] As red phosphorescent light-emitting materials that can be used in the light-emitting layer, metal complexes such as iridium complexes, platinum complexes, terbium complexes, and europium complexes are used. Specific examples of the organic metal complex include bis[2-(2'-benzo[4,5-α]thienyl)pyridinato-N,C3']iridium(III) acetylacetonate (abbreviation: Ir(btp)2(acac)), bis(1-phenylisoquinolinato-N,C2')iridium(III) acetylacetonate (abbreviation: Ir(piq)2(acac)), (acetylacetonato)bis[2,3-bis(4-fluorophenyl)quinoxalinato]iridium(III) (abbreviation: Ir(Fdpq)2(acac)), and 2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphyrin platinum(II) (abbreviation: PtOEP).

[0219] In addition, rare earth metal complexes such as tris(acetylacetonato)(monophenanthroline)terbium(III) (abbreviation: Tb(acac)3(Phen)), tris(1,3-diphenyl-1,3-propanedionato)(monophenanthroline)europium(III) (abbreviation: Eu(DBM)3(Phen)), and tris[1-(2-thenoyl)-3,3,3-trifluoroacetonato](monophenanthroline)europium(III) (abbreviation: Eu(TTA)3(Phen)) can be used as phosphorescent materials because they emit light from rare earth metal ions (electron transition between different multiplicities).

[0220] Host material for the emissive layer The light-emitting layer may be configured by dispersing the above-mentioned dopant material in another material (host material). It is preferable to use a material having a lower lowest unoccupied molecular orbital (LUMO) level and a lower highest occupied molecular orbital (HOMO) level than the dopant material.

[0221] Examples of the host material include (1) Metal complexes such as aluminum complexes, beryllium complexes, or zinc complexes, (2) Heterocyclic compounds such as oxadiazole derivatives, benzimidazole derivatives, or phenanthroline derivatives, (3) Condensed aromatic compounds such as carbazole derivatives, anthracene derivatives, phenanthrene derivatives, pyrene derivatives, and chrysene derivatives; (4) An aromatic amine compound such as a triarylamine derivative or a condensed polycyclic aromatic amine derivative is used.

[0222] For example, metal complexes such as tris(8-quinolinolato)aluminum(III) (abbreviation: Alq), tris(4-methyl-8-quinolinolato)aluminum(III) (abbreviation: Almq3), bis(10-hydroxybenzo[h]quinolinato)beryllium(II) (abbreviation: BeBq2), bis(2-methyl-8-quinolinolato)(4-phenylphenolato)aluminum(III) (abbreviation: BAlq), bis(8-quinolinolato)zinc(II) (abbreviation: Znq), bis[2-(2-benzoxazolyl)phenolato]zinc(II) (abbreviation: ZnPBO), and bis[2-(2-benzothiazolyl)phenolato]zinc(II) (abbreviation: ZnBTZ); Heterocyclic compounds such as 2-(4-biphenylyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole (abbreviation: PBD), 1,3-bis[5-(p-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]benzene (abbreviation: OXD-7), 3-(4-biphenylyl)-4-phenyl-5-(4-tert-butylphenyl)-1,2,4-triazole (abbreviation: TAZ), 2,2',2''-(1,3,5-benzenetriyl)tris(1-phenyl-1H-benzimidazole) (abbreviation: TPBI), bathophenanthroline (abbreviation: BPhen), and bathocuproine (abbreviation: BCP); 9-[4-(10-phenyl-9-anthryl)phenyl]-9H-carbazole (abbreviation: CzPA), 3,6-diphenyl-9-[4-(10-phenyl-9-anthryl)phenyl]-9H-carbazole (abbreviation: DPCzPA), 9,10-bis(3,5-diphenylphenyl)anthracene (abbreviation: DPPA), 9,10-di(2-naphthyl)anthracene (abbreviation: DNA), 2-tert-butyl-9,10-di(2-naphthyl)anthracene (abbreviation: t-Bu condensed aromatic compounds such as DNA), 9,9'-bianthryl (abbreviation: BANT), 9,9'-(stilbene-3,3'-diyl)diphenanthrene (abbreviation: DPNS), 9,9'-(stilbene-4,4'-diyl)diphenanthrene (abbreviation: DPNS2), 3,3',3''-(benzene-1,3,5-triyl)tripylene (abbreviation: TPB3), 9,10-diphenylanthracene (abbreviation: DPAnth), and 6,12-dimethoxy-5,11-diphenylchrysene; and N,N-diphenyl-9-[4-(10-phenyl-9-anthryl)phenyl]-9H-carbazol-3-amine (abbreviation: CzA1PA), 4-(10-phenyl-9-anthryl)triphenylamine (abbreviation: DPhPA), N,9-diphenyl-N-[4-(10-phenyl-9-anthryl)phenyl]-9H-carbazol-3-amine (abbreviation: PCAPA), N,9-diphenyl-N-{4-[4-(10-phenyl-9-anthryl)phenyl]phenyl}-9H-carbazol-3-amine (abbreviation: PCAPBA), N-(9,10-diphenyl-2-anthryl)-N,9-diphenyl-9H Aromatic amine compounds such as -carbazole-3-amine (abbreviation: 2PCAPA), 4,4'-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (abbreviation: NPB or α-NPD), N,N'-bis(3-methylphenyl)-N,N'-diphenyl-[1,1'-biphenyl]-4,4'-diamine (abbreviation: TPD), 4,4'-bis[N-(9,9-dimethylfluoren-2-yl)-N-phenylamino]biphenyl (abbreviation: DFLDPBi), and 4,4'-bis[N-(spiro-9,9'-bifluoren-2-yl)-N-phenylamino]biphenyl (abbreviation: BSPB) can be used. Multiple host materials may be used.

[0223] In particular, in the case of a blue fluorescent element, it is preferable to use the following anthracene compound as the host material.

[0224] [ka]

[0225] [ka]

[0226] [ka]

[0227] electron transport layer The electron transport layer is a layer containing a material with high electron transporting properties (electron transporting material), and is formed between the light emitting layer and the cathode, or, if present, between the electron injection layer and the light emitting layer. The compounds of the invention are preferably used in the electron transport layer either alone or in combination with the following compounds:

[0228] The electron transport layer may have a single-layer structure or a multi-layer structure including two or more layers. For example, the electron transport layer may have a two-layer structure including a first electron transport layer (anode side) and a second electron transport layer (cathode side). In one embodiment of the present invention, the electron transport layer of the single-layer structure is preferably adjacent to the light-emitting layer, and the electron transport layer closest to the anode in the multi-layer structure, for example, the first electron transport layer of the two-layer structure, is preferably adjacent to the light-emitting layer. In another embodiment of the present invention, a hole blocking layer, which will be described later, may be interposed between the electron transport layer and the light-emitting layer of the single-layer structure, or between the electron transport layer closest to the light-emitting layer and the light-emitting layer in the multi-layer structure. In the electron transport layer of the two-layer structure, the compound of the invention may be contained in either the first electron transport layer or the second electron transport layer, or in both layers. In one embodiment of the invention, the compound of the invention is preferably contained only in the first electron transport layer adjacent to the light-emitting layer, in another embodiment, the compound of the invention is preferably contained only in the second electron transport layer, and in yet another embodiment, the compound of the invention is preferably contained in both the first electron transport layer and the second electron transport layer.

[0229] In one embodiment of the present invention, the compound of the invention contained in one or both of the first electron transport layer and the second electron transport layer is preferably a protolytic compound from the viewpoint of production costs. The proton derivative refers to a compound of the invention in which all hydrogen atoms in the formula (1) are proton atoms. Therefore, the present invention includes an organic EL device in which one or both of the first electron transport layer and the second electron transport layer contain an invention compound substantially composed of protium compounds. The "invention compound substantially composed of protium compounds" means that the content of protium compounds relative to the total amount of the compound represented by formula (1) is 90 mol % or more, preferably 95 mol % or more, and more preferably 99 mol % or more (each including 100%).

[0230] In addition to the compound of the present invention, the electron transport layer may further include, for example, (1) Metal complexes such as aluminum complexes, beryllium complexes, and zinc complexes, (2) Heteroaromatic compounds such as imidazole derivatives, benzimidazole derivatives, azine derivatives, carbazole derivatives, and phenanthroline derivatives; (3) Polymer compounds can be used.

[0231] Examples of metal complexes include tris(8-quinolinolato)aluminum(III) (abbreviation: Alq), tris(4-methyl-8-quinolinolato)aluminum (abbreviation: Almq3), bis(10-hydroxybenzo[h]quinolinato)beryllium (abbreviation: BeBq2), bis(2-methyl-8-quinolinolato)(4-phenylphenolato)aluminum(III) (abbreviation: BAlq), bis(8-quinolinolato)zinc(II) (abbreviation: Znq), bis[2-(2-benzoxazolyl)phenolato]zinc(II) (abbreviation: ZnPBO), and bis[2-(2-benzothiazolyl)phenolato]zinc(II) (abbreviation: ZnBTZ).

[0232] Examples of heteroaromatic compounds include 2-(4-biphenylyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole (abbreviation: PBD), 1,3-bis[5-(ptert-butylphenyl)-1,3,4-oxadiazol-2-yl]benzene (abbreviation: OXD-7), 3-(4-tert-butylphenyl)-4-phenyl-5-(4-biphenylyl)-1,2,4-triazole (abbreviation: TAZ), 3-(4-tert-butylphenyl)-4-(4-ethylphenyl)-5-(4-biphenylyl)-1,2,4-triazole (abbreviation: p-EtTAZ), bathophenanthroline (abbreviation: BPhen), bathocuproine (abbreviation: BCP), and 4,4'-bis(5-methylbenzoxazol-2-yl)stilbene (abbreviation: BzOs).

[0233] Examples of polymer compounds include poly[(9,9-dihexylfluorene-2,7-diyl)-co-(pyridine-3,5-diyl)] (abbreviation: PF-Py) and poly[(9,9-dioctylfluorene-2,7-diyl)-co-(2,2'-bipyridine-6,6'-diyl)] (abbreviation: PF-BPy).

[0234] The above materials are 10 -6 cm 2 A material having an electron mobility of 1 / Vs or more. Note that materials other than those mentioned above may be used for the electron transport layer as long as they have a higher electron transporting property than a hole transporting property.

[0235] electron injection layer The electron injection layer is a layer containing a material with high electron injection properties (electron injection material) and is formed between the cathode and the light emitting layer, or, if present, between the electron transport layer and the cathode. The compound of the invention may be used in the electron injection layer.

[0236] As the electron injection material other than the compound of the invention, alkali metals such as lithium (Li) and cesium (Cs), alkaline earth metals such as magnesium (Mg), calcium (Ca), and strontium (Sr), rare earth metals such as europium (Eu) and ytterbium (Yb), and compounds containing these metals can be used. Examples of such compounds include alkali metal oxides, alkali metal halides, alkali metal-containing organic complexes, alkaline earth metal oxides, alkaline earth metal halides, alkaline earth metal-containing organic complexes, rare earth metal oxides, rare earth metal halides, and rare earth metal-containing organic complexes. In addition, a mixture of a plurality of these compounds can be used. In addition, materials having electron transport properties containing alkali metals, alkaline earth metals, or compounds thereof, specifically, materials containing magnesium (Mg) in Alq, etc., may be used. In this case, electron injection from the cathode can be performed more efficiently. Alternatively, a composite material obtained by mixing an organic compound and an electron donor (donor) may be used for the electron injection layer. Such a composite material has excellent electron injection and transport properties because the organic compound receives electrons from the electron donor. In this case, the organic compound is preferably a material that is excellent in transporting the received electrons, and specifically, for example, the above-mentioned materials constituting the electron transport layer (metal complexes, heteroaromatic compounds, etc.) can be used. The electron donor may be any material that exhibits electron donating properties to the organic compound. Specifically, alkali metals, alkaline earth metals, and rare earth metals are preferred, and examples of such materials include lithium, cesium, magnesium, calcium, erbium, and ytterbium. Furthermore, alkali metal oxides and alkaline earth metal oxides are preferred, and examples of such materials include lithium oxide, calcium oxide, and barium oxide. Furthermore, a Lewis base such as magnesium oxide can also be used. Furthermore, an organic compound such as tetrathiafulvalene (abbreviation: TTF) can also be used.

[0237] cathode For the cathode, it is preferable to use a metal, alloy, electrically conductive compound, or a mixture thereof, each having a small work function (specifically, 3.8 eV or less). Specific examples of such a cathode material include elements belonging to Group 1 or 2 of the periodic table, i.e., alkali metals such as lithium (Li) and cesium (Cs), alkaline earth metals such as magnesium (Mg), calcium (Ca), and strontium (Sr), and alloys containing these (e.g., MgAg, AlLi), rare earth metals such as europium (Eu), ytterbium (Yb), and alloys containing these. When an alkali metal, an alkaline earth metal, or an alloy containing these is used to form a cathode, a vacuum deposition method or a sputtering method can be used. When a silver paste or the like is used, a coating method or an inkjet method can be used. By providing an electron injection layer, the cathode can be formed using various conductive materials, such as Al, Ag, ITO, graphene, indium oxide-tin oxide containing silicon or silicon oxide, regardless of the magnitude of the work function. These conductive materials can be formed into films by a sputtering method, an inkjet method, a spin coating method, or the like.

[0238] Insulation layer In organic EL devices, pixel defects due to leakage and short circuits are likely to occur because an electric field is applied to an ultra-thin film. To prevent this, an insulating layer made of an insulating thin film may be inserted between a pair of electrodes. Examples of materials used for the insulating layer include aluminum oxide, lithium fluoride, lithium oxide, cesium fluoride, cesium oxide, magnesium oxide, magnesium fluoride, calcium oxide, calcium fluoride, aluminum nitride, titanium oxide, silicon oxide, germanium oxide, silicon nitride, boron nitride, molybdenum oxide, ruthenium oxide, vanadium oxide, etc. Mixtures or laminates of these materials may also be used.

[0239] Space Layer The spacer layer is a layer provided between a fluorescent light-emitting layer and a phosphorescent light-emitting layer for the purpose of preventing excitons generated in the phosphorescent light-emitting layer from diffusing into the fluorescent light-emitting layer or for the purpose of adjusting the carrier balance when the fluorescent light-emitting layer and the phosphorescent light-emitting layer are laminated, for example. The spacer layer can also be provided between a plurality of phosphorescent light-emitting layers. Since the spacer layer is provided between the light-emitting layers, it is preferable that the spacer layer is made of a material having both electron transport properties and hole transport properties. In addition, in order to prevent the diffusion of triplet energy in the adjacent phosphorescent light-emitting layer, it is preferable that the triplet energy is 2.6 eV or more. Materials used for the spacer layer include the same materials as those used for the hole transport layer described above.

[0240] blocking layer A blocking layer such as an electron blocking layer, a hole blocking layer, or an exciton blocking layer may be provided adjacent to the light-emitting layer. The electron blocking layer is a layer that prevents electrons from leaking from the light-emitting layer to the hole transport layer, and the hole blocking layer is a layer that prevents holes from leaking from the light-emitting layer to the electron transport layer. In one embodiment, the inventive compound is preferably used as the hole blocking layer. The exciton blocking layer has the function of preventing excitons generated in the light-emitting layer from diffusing into the surrounding layers and confining the excitons within the light-emitting layer.

[0241] Each layer of the organic EL element can be formed by a conventionally known deposition method, coating method, etc. For example, the layers can be formed by a conventionally known deposition method such as vacuum deposition method or molecular beam deposition method (MBE method), or a coating method such as dipping method, spin coating method, casting method, bar coating method, or roll coating method using a solution of a compound that forms the layer.

[0242] The thickness of each layer is not particularly limited, but generally, if the thickness is too thin, defects such as pinholes are likely to occur, while if the thickness is too thick, a high driving voltage is required, resulting in poor efficiency. Therefore, the thickness is usually 5 nm to 10 μm, and more preferably 10 nm to 0.2 μm.

[0243] The organic EL element can be used in display components such as organic EL panel modules, display devices for televisions, mobile phones, personal computers, and electronic devices such as light-emitting devices for lighting and vehicle lamps. EXAMPLES

[0244] The present invention will be described in more detail below using examples, but the present invention is not limited to the following examples.

[0245] Compounds of the invention used in the manufacture of organic EL devices in Examples 1 to 19 below [ka] [ka] [ka] [ka]

[0246] Comparative compounds used in the manufacture of organic EL devices in Comparative Examples 1 to 3 below [ka]

[0247] Other compounds used in the manufacture of organic EL devices in Examples 1 to 19 and Comparative Examples 1 to 3 below [ka]

[0248] Each organic EL device was prepared as follows, and the EL device performance of each device was evaluated.

[0249] Fabrication of organic electroluminescence devices Example 1 A 25 mm x 75 mm x 1.1 mm glass substrate with an ITO transparent electrode (anode) (manufactured by Geomatec Co., Ltd.) was ultrasonically cleaned in isopropyl alcohol for 5 minutes, and then UV ozone cleaned for 30 minutes. The ITO film thickness was 130 nm. The glass substrate with the transparent electrode lines after cleaning was attached to a substrate holder of a vacuum deposition apparatus, and the compound HT-1 and the compound HI-1 were co-deposited on the surface on which the transparent electrode lines were formed so as to cover the transparent electrode, thereby forming a hole injection layer with a thickness of 10 nm. The mass ratio of the compound HT-1 to the compound HI-1 was 97:3. Next, the compound HT-1 was deposited on the hole injection layer to form a first hole transport layer having a thickness of 80 nm. Next, compound EBL-1 was deposited on the first hole transport layer to form a second hole transport layer (electron blocking layer) having a thickness of 10 nm. Next, on the second hole transport layer (electron blocking layer), compound BH-1 (host material) and compound BD-1 (dopant material) were co-deposited to form a light emitting layer having a thickness of 25 nm. The mass ratio of compound BH-1 to compound BD-1 was 96:4. Next, compound 1 (HBL-1) was deposited on the light-emitting layer to form a hole-blocking layer having a thickness of 10 nm. Compound ET-1 was evaporated to form an electron transport layer having a thickness of 15 nm. Next, Yb was evaporated onto this electron transport layer to form an electron injecting electrode (cathode) having a thickness of 1 nm. Then, metallic Al was evaporated onto this electron injecting electrode to form a metal cathode with a thickness of 80 nm. The organic EL element of Example 1 thus obtained had the following layer structure. ITO (130) / HT-1:HI-1 = 97:3 (10) / HT-1 (80) / EBL-1 (10) / BH-1:BD-1 = 96:4 (25) / HBL-1 (10) / ET-1 (15) / Yb (1) / Al (80) In the above layer structure, the numbers in parentheses indicate film thickness (nm), and the ratio of HT-1 to HI-1 and the ratio of BH-1 to BD-1 are mass ratios.

[0250] Examples 2 to 19 Organic EL devices of Examples 2 to 19 were prepared in the same manner as in Example 1, except that Compound 2 (HBL-2) to Compound 19 (HBL-19) were used in the hole blocking layer in place of Compound 1 (HBL-1), in that order.

[0251] Comparative Examples 1 to 3 Organic EL devices of Comparative Examples 1 to 3 were prepared in the same manner as in Example 1, except that Comparative Compound 1 (HBL-A), Comparative Compound 2 (HBL-B), and Comparative Compound 3 (HBL-C) were used in this order instead of Compound 1 (HBL-1) in the hole blocking layer.

[0252] Evaluation of organic EL elements The life span of each of the produced organic EL devices was evaluated. The evaluation results are shown in Table 1.

[0253] Element life (LT95) The resulting organic EL device was subjected to a current density of 50 mA / cm 2 The time until the luminance decreased to 95% of the initial luminance was measured, and this was taken as LT95 (95% life span).

[0254] [Table 1]

[0255] Evaluation of glass transition temperature Tg The glass transition temperature Tg of the compound used in the hole blocking layer was evaluated. The glass transition temperature was measured using a differential scanning calorimeter DSC7000X (Hitachi High-Tech Science Corporation) according to the method specified in JIS K7121 (1987). The measurement results are shown in Table 2.

[0256] [Table 2]

[0257] As is clear from the results in Tables 1 and 2, the compounds of the present invention, which have a structure in which a specific carbazole skeleton is bonded to a pyrimidine skeleton via a single bond or an arylene group and further via a naphthylene group, have a molecular weight of 650 or more, and a high glass transition temperature, showed a more improved element life than Comparative Compounds 1 to 3, which do not satisfy the structural conditions or molecular weight of the present invention.

[0258] <Synthesis of Compounds> Synthesis of intermediate A [ka]

[0259] 4-Bromo-1-naphthaldehyde (9.0 g), acetophenone (4.6 g), and sodium hydroxide (0.15 g) were added to 300 mL of ethanol and stirred at room temperature for 5 hours. Next, benzamidine hydrochloride (6.0 g) and sodium hydroxide (1.8 g) were added and stirred at 70°C for 5 hours. After the reaction was completed, the precipitate was filtered and purified by silica gel column chromatography (developing solvent: hexane / toluene) to obtain intermediate A as a white solid (7.6 g, yield 45%).

[0260] Synthesis Example 1: Synthesis of Compound 1 [ka]

[0261] Intermediate A (5.0 g) and [4'-(carbazol-9-yl)-4-biphenylyl]boronic acid (4.5 g) were added to 1,2-dimethoxyethane (80 mL), and argon gas was passed through the solution for 5 minutes. Pd(PPh3)4 (0.4 g) and aqueous sodium carbonate solution (2 M, 12 mL) were added to the solution, and the mixture was heated under reflux for 7 hours while stirring under an argon atmosphere. The solvent was removed from the reaction solution, and the resulting solid was purified by silica gel column chromatography (developing solvent: hexane / toluene) to obtain HBL-1 as a white solid (6.6 g, 85% yield). Mass spectrum analysis showed that the molecular weight was 675.84 and m / e was 676, indicating that the compound was identified as HBL-1.

[0262] Synthesis of intermediate B [ka]

[0263] 4-Bromo-1-naphthaldehyde (8.0 g), 4-acetylbiphenyl (7.0 g), and sodium hydroxide (0.27 g) were added to 600 mL of ethanol and stirred at room temperature for 5 hours. Next, benzamidine hydrochloride (8.0 g) and sodium hydroxide (2.7 g) were added and stirred at 70°C for 5 hours. After the reaction was completed, the precipitate was filtered and purified by silica gel column chromatography (developing solvent: hexane / toluene) to obtain intermediate B as a white solid (5.0 g, yield 28%).

[0264] Synthesis Example 2: Synthesis of Compound 2 [ka]

[0265] Using intermediate B (5.0 g), HBL-2 ​​was obtained as a white solid (4.5 g, yield 68%) by the same synthesis method as in Synthesis Example 1. As a result of mass spectrometry analysis, the molecular weight was 675.84 and m / e was 676, so that it was identified as compound 2 (HBL-2).

[0266] Synthesis of intermediate C [ka]

[0267] Using intermediate A (10.0 g) and 4-fluorophenylboronic acid (3.5 g), intermediate C was obtained as a white solid (9.0 g, yield 83%) by the same method as in Synthesis Example 1.

[0268] Synthesis Example 3: Synthesis of Compound 3 [ka]

[0269] Intermediate C (3.8 g), 3,6-diphenylcarbazole (4.0 g), and cesium carbonate (8.2 g) were added to 30 mL of N-methylpyrrolidone (NMP) and stirred at 160°C for 24 hours. After cooling the reaction solution to room temperature, 100 mL of methanol and 100 mL of water were added and stirred at room temperature for 1 hour. The precipitated solid was collected by filtration and purified by silica gel column chromatography (developing solvent: hexane / toluene) to obtain HBL-3 as a white solid (6.3 g, yield 94%). As a result of mass spectrometry analysis, the molecular weight was 751.93 and m / e was 752, so it was identified as compound 3 (HBL-3).

[0270] Synthesis of intermediate D [ka]

[0271] Using intermediate A (5.0 g) and 3,5-difluorophenylboronic acid (2.0 g), intermediate D was obtained as a white solid (4.2 g, yield 78%) in the same manner as in Synthesis Example 1.

[0272] Synthesis Example 4: Synthesis of Compound 4 [ka]

[0273] Using intermediate D (4.2 g) and carbazole (4.5 g), HBL-4 was obtained as a white solid (4.1 g, yield 60%) by the same method as in Synthesis Example 3. As a result of mass spectrometry analysis, the molecular weight was 764.93 and m / e was 765, so that it was identified as compound 4 (HBL-4).

[0274] Synthesis Example 5: Synthesis of Compound 5 [ka]

[0275] Using intermediate A (3.9 g) and 9-phenyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-9H-carbazole (4.0 g), HBL-5 was obtained as a white solid (4.7 g, yield 78%) by the same method as in Synthesis Example 1. As a result of mass spectrum analysis, the molecular weight was 675.84 and m / e was 676, so that it was identified as compound 5 (HBL-5).

[0276] Synthesis Example 6: Synthesis of Compound 6 [ka]

[0277] Intermediate A (6.0 g), 3,6-diphenylcarbazole (4.2 g), palladium acetate (0.48 g), Amphos (1.3 g), and t-BuONa (3.8 g) were added to 168 mL of dehydrated xylene and stirred under reflux for 36 hours. After the reaction solution was cooled to room temperature, 100 mL of methanol and 100 mL of water were added and stirred at room temperature for 1 hour. The precipitated solid was collected by filtration and purified by silica gel column chromatography (developing solvent: hexane / toluene) to obtain HBL-6 as a white solid (4.8 g, yield 52%). Mass spectrometry revealed that the m / e was 675 for a molecular weight of 675.84, and thus the compound was identified as compound 6 (HBL-6).

[0278] Synthesis Example 7: Synthesis of Compound 7 [ka]

[0279] Using intermediate C (5.6 g) under the same conditions as described in Synthesis Example 3, HBL-7 was obtained as a white solid (5.9 g, 61% yield). Mass spectrometry revealed that the molecular weight was 675.84 with m / e=675, and the compound was identified as compound 7 (HBL-7).

[0280] Synthesis Example 8: Synthesis of Compound 8 [ka]

[0281] Using intermediate E (8.0 g) synthesized according to the synthesis method of intermediate B using 3-acetylbiphenyl as a starting material, HBL-8 was obtained as a white solid (10.3 g, yield 87%) under the same conditions as described in Synthesis Example 1. Mass spectrometry revealed that the m / e was 675 for a molecular weight of 675.84, and thus the compound was identified as compound 8 (HBL-8).

[0282] Synthesis Example 9: Synthesis of Compound 9 [ka]

[0283] Using intermediate E (5.0 g) and intermediate F (3.6 g), under the same conditions as those described in Synthesis Example 1, HBL-9 was obtained as a white solid (5.7 g, yield 78%). Mass spectrometry revealed that the m / e was 751 for a molecular weight of 751.93, and thus the compound was identified as compound 9 (HBL-9).

[0284] Synthesis Example 10: Synthesis of Compound 10 [ka]

[0285] Using intermediate B (4.0 g) and intermediate F (2.8 g), HBL-10 was obtained as a white solid (5.1 g, 87% yield) under the same conditions as those described in Synthesis Example 1. Mass spectrometry revealed that the m / e was 751 for a molecular weight of 751.93, and thus the compound was identified as compound 10 (HBL-10).

[0286] Synthesis of intermediate G [ka]

[0287] Using intermediate A (10.0 g) and 4-chlorophenylboronic acid (3.6 g), intermediate G was obtained as a white solid (9.8 g, 91% yield) under the same conditions as those described in Synthesis Example 1.

[0288] Synthesis Example 11: Synthesis of Compound 11 [ka]

[0289] Intermediate G (4.5 g), N-phenylcarbazole-2-boronic acid (4.1 g), and tripotassium phosphate (8.2 g) were added to 1,4-dioxane (100 mL), and argon gas was passed through the solution for 5 minutes. Pd2(dba)3 (0.18 g) and SPhos (0.32 g) were added to the solution, and the mixture was heated under reflux for 24 hours while stirring under an argon atmosphere. The solvent was removed from the reaction solution, and the resulting solid was purified by silica gel column chromatography (developing solvent: hexane / toluene) to obtain HBL-11 as a white solid (5.8 g, yield 90%). Mass spectrometry revealed that the m / e was 675 for a molecular weight of 675.84, and thus the compound was identified as compound 11 (HBL-11).

[0290] Synthesis Example 12: Synthesis of Compound 12 [ka]

[0291] Using intermediate G (3.5 g) and N-phenylcarbazole-4-boronic acid (3.2 g), under the same conditions as described in Synthesis Example 11, HBL-12 was obtained as a white solid (3.1 g, 62% yield). Mass spectrometry revealed that the molecular weight was 675.84 with m / e=675, and the compound was identified as compound 12 (HBL-12).

[0292] Synthesis of intermediate H [ka]

[0293] Using intermediate A (5.0 g) and 3,4-difluorophenylboronic acid (2.5 g), intermediate H was obtained as a white solid (4.3 g, 80% yield) under the same conditions as described in Synthesis Example 1.

[0294] Synthesis Example 13 Synthesis of Compound 13 [ka]

[0295] Using intermediate H (4.3 g) under the same conditions as described in Synthesis Example 3, HBL-13 was obtained as a white solid (5.5 g, 79% yield). Mass spectrometry revealed that the molecular weight was 764.93 with m / e=764, and the compound was identified as compound 13 (HBL-13).

[0296] Synthesis of intermediate I [ka]

[0297] Using intermediate A (5.0 g) and 3-fluorophenylboronic acid (2.2 g), intermediate I was obtained as a white solid (4.8 g, 92% yield) under the same conditions as described in Synthesis Example 1.

[0298] Synthesis Example 14: Synthesis of Compound 14 [ka]

[0299] Using intermediate I (4.8 g) and 3,6-diphenylcarbazole (5.0 g), under the same conditions as those described in Synthesis Example 3, HBL-14 was obtained as a white solid (7.2 g, 90% yield). Mass spectrometry revealed that the m / e was 751 for a molecular weight of 751.93, and thus the compound was identified as compound 14 (HBL-14).

[0300] Synthesis Example 15: Synthesis of Compound 15 [ka]

[0301] Using intermediate B (4.0 g) and [4'-(carbazol-9-yl)-4-biphenylyl]boronic acid (3.4 g), HBL-15 was obtained as a white solid (5.0 g, 76% yield) under the same conditions as described in Synthesis Example 1. Mass spectrometry revealed that the m / e was 751 for a molecular weight of 751.93, and thus the compound was identified as compound 15 (HBL-15).

[0302] Synthesis Example 16: Synthesis of Compound 16 [ka]

[0303] Using intermediate B (4.5 g) and N-phenylcarbazole-4-boronic acid (3.0 g), under the same conditions as those described in Synthesis Example 1, HBL-16 was obtained as a white solid (5.5 g, yield 92%). Mass spectrometry revealed that the molecular weight was 675.84 with m / e=675, and the compound was identified as compound 16 (HBL-16).

[0304] Synthesis Example 17: Synthesis of Compound 17 [ka]

[0305] Using intermediate B (5.0 g) and 3-(N-carbazole)phenylboronic acid (3.4 g), under the same conditions as those described in Synthesis Example 1, HBL-17 was obtained as a white solid (5.6 g, yield 85%). Mass spectrum analysis showed that the m / e was 675 for a molecular weight of 675.84, and thus the compound was identified as compound 17 (HBL-17).

[0306] Synthesis of intermediate J [ka]

[0307] Using intermediate B (5.0 g) and 4-fluorophenylboronic acid (1.6 g), intermediate J was obtained as a white solid (4.5 g, 87% yield) under the same conditions as described in Synthesis Example 1.

[0308] Synthesis Example 18: Synthesis of Compound 18 [ka]

[0309] Using intermediate J (4.5 g) and carbazole-d8 (2.2 g), under the same conditions as described in Synthesis Example 3, HBL-18 was obtained as a white solid (3.8 g, 65% yield). Mass spectrometry revealed that the molecular weight was 683.88 and the m / e was 683, indicating that the compound was compound 18 (HBL-18).

[0310] Synthesis of intermediate K [ka]

[0311] Following the procedure for the synthesis of Intermediate A, but using acetophenone(phenyl-d5) (4.8 g) instead of acetophenone, Intermediate K was obtained as a white solid (5.1 g, 30% yield).

[0312] Synthesis Example 19: Synthesis of Compound 19 [ka]

[0313] Using intermediate K (3.0 g) and [4'-(carbazol-9-yl)-4-biphenylyl]boronic acid (2.5 g), HBL-19 was obtained as a white solid (2.0 g, 43% yield) under the same conditions as described in Synthesis Example 1. Mass spectrum analysis showed that the m / e was 680 for a molecular weight of 680.87, and thus the compound was identified as compound 19 (HBL-19).

[0314] The compounds of the present invention can also be synthesized via the following synthetic intermediates according to the conditions described in the synthesis examples. [ka] [ka] [ka] [ka] [ka] [ka] [ka] [Explanation of symbols]

[0315] 1, 11 Organic EL element 2. Board 3 Anode 4 cathode 5. Light-emitting layer 6 Hole transport zone (hole injection layer, hole transport layer, etc.) 7 Electron transport zone (electron injection layer, electron transport layer, etc.) 7a Hole blocking layer 7b Electron transport layer 7c Electron injection layer 10, 20 Light Emitting Units

Claims

1. A compound represented by the following formula (1), wherein the molecular weight of the compound is 650 or more. 【Chemistry 1】 (In the formula, Y １ and Y ２ one is a nitrogen atom and the other is CR; R is a hydrogen atom; Ar １ and Ar ２ each independently represents a substituted or unsubstituted aryl group having 6 to 18 ring carbon atoms; L １ and L ２ are each independently a single bond or a substituted or unsubstituted arylene group having 6 to 18 ring carbon atoms. R １ ~R ６ are all hydrogen atoms. Cz is represented by the following formula (1-a) or formula (1-b): 【Chemistry 2】 During the ceremony, R ２１ ~R ２８ and R ３１ ~R ３８ are each independently a hydrogen atom or a substituent, and the substituent is selected from a substituted or unsubstituted phenyl group and a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; However, R ２１ ~R ２８ Two adjacent ones selected from R ３１ ~R ３８ Two adjacent ones selected from R ２４ and R ２５ and R ３４ and R ３５ do not bond to each other to form a ring. R ａ is selected from a substituted or unsubstituted aryl group having 6 to 18 ring carbon atoms and a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; R ２１ ~R ２８ One selected from *a is L ３ is a single bond linking *b is L ３ represents the position at which the molecule binds to the molecule. n is an integer of 1 to 2, and when n is an integer of 2, two Cz are the same or different from each other; L ３ and L ４ are each independently a single bond or a substituted or unsubstituted arylene group having 6 to 18 ring carbon atoms, and the unsubstituted arylene group is selected from a phenylene group, a biphenylene group, a naphthylene group, a phenanthrylene group, and an anthracenylene group. However, when n is an integer of 2, L ４ represents a substituted or unsubstituted arylene group having 6 to 18 ring carbon atoms, and the unsubstituted arylene group is selected from a phenylene group, a biphenylene group, a naphthylene group, a phenanthrylene group, and an anthracenylene group. However, in the case of "substituted or unsubstituted", the substituent is selected from an unsubstituted alkyl group having 1 to 6 carbon atoms, an unsubstituted cycloalkyl group having 3 to 6 ring carbon atoms, and an unsubstituted aryl group having 6 to 18 ring carbon atoms.

2. L ３ and L ４ are each independently a substituted or unsubstituted arylene group having 6 to 18 ring carbon atoms, and the unsubstituted arylene group having 6 to 18 ring carbon atoms is selected from a phenylene group, a biphenylene group, a naphthylene group, a phenanthrylene group, and an anthracenylene group.

3. *L through a ３ R that is not a single bond bonded to ２１ ~R ２８ At least one selected from, or R ３１ ~R ３８ The compound according to claim 1 or 2, wherein at least one selected from the following is a substituent.

4. *L through a ３ R that is not a single bond bonded to ２１ ~R ２８ and R ３１ ~R ３８ The compound according to any one of claims 1 to 3, wherein at least one of the substituents represented by the formula (I) is selected from a substituted or unsubstituted phenyl group and a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms.

5. *L through a ３ R that is not a single bond bonded to ２１ ~R ２８ and R ３１ ~R ３８ The compound according to any one of claims 1 to 4, wherein at least one of the substituents represented by is selected from a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, an s-butyl group, a t-butyl group, and a phenyl group.

6. The compound according to any one of claims 1 to 5, represented by formula (1-b-1) or (1-b-2): 【Chemistry 3】 (In the formula, Y １ , Y ２ , Ar １ , Ar ２ , L １ , L ２ and R １ ~R ６ is as defined in formula (1), R ３１ ~R ３８ is as defined in formula (1-b), and R ４１ ~R ４２ , R ４４ ~R ４５ , R ５１ ~R ５２ and R ５４ ~R ５５ are each independently selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 18 ring carbon atoms, and a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms.

7. The compound according to any one of claims 1 to 6, represented by any one of formulas (1-b-11) to (1-b-14). 【Chemistry 4】 (In the formula, Y １ , Y ２ , Ar １ , Ar ２ , L １ , L ２ and R １ ~R ６ is as defined in formula (1), R ３１ ~R ３８ is as defined in formula (1-b), and R ４１ and R ４４ ~R ４５ is as defined in formula (1-b-1). ４３ is selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 18 ring carbon atoms, and a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms.

8. The compound according to any one of claims 1 to 5, represented by any one of formulas (1-a-1) to (1-a-4): 【Chemistry 5】 (In the formula, Y １ , Y ２ , Ar １ , Ar ２ , L １ , L ２ and R １ ~R ６ is as defined in formula (1), R ２１ ~R ２８ is as defined in formula (1-a), and R ４１ ~R ４２ and R ４４ ~R ４５ is as defined in formula (1-b-1).

9. L １ and L ２ wherein one of is a substituted or unsubstituted arylene group having 6 to 18 ring carbon atoms, and the remaining one is a single bond.

10. L １ and L ２ and each independently represents a substituted or unsubstituted arylene group having 6 to 18 ring carbon atoms.

11. L １ and L ２ The compound according to any one of claims 1 and 6 to 10, wherein the unsubstituted arylene groups in the substituted or unsubstituted arylene group having 6 to 18 ring carbon atoms represented by the formula (I) are each independently selected from a phenylene group, a biphenylene group, a naphthylene group, a phenanthrylene group, a fluorenylene group, and an anthracenylene group.

12. Ar １ and Ar ２ The compound according to any one of claims 1 and 6 to 8, wherein the unsubstituted aryl groups in the substituted or unsubstituted aryl groups having 6 to 18 ring carbon atoms represented by the formula (I) are each independently selected from a phenyl group, a biphenyl group, a naphthyl group, a phenanthryl group, an anthracenyl group, a chrysenyl group and a pyrenyl group.

13. R ａ The compound according to claim 1 or 8, wherein the unsubstituted aryl group in the substituted or unsubstituted aryl group having 6 to 18 ring carbon atoms represented by the formula (I) is selected from a phenyl group, a biphenyl group, a naphthyl group, and a phenanthryl group.

14. R ４１ ~R ４５ The compound according to any one of claims 1 and 6 to 8, wherein all of are hydrogen atoms.

15. R ５１ ~R ５２ and R ５４ ~R ５５ The compound according to claim 1 or 6, wherein all of are hydrogen atoms.

16. *L through a ３ R that is not a single bond bonded to ２１ ~R ２８ The compound according to any one of claims 1, 3 to 5 and 8, wherein all of the substituents other than the substituent selected from are hydrogen atoms.

17. R ３１ ~R ３８ The compound according to any one of claims 1 and 3 to 7, wherein all of the substituents other than the substituent selected from are hydrogen atoms.

18. The compound according to any one of claims 1 to 17, comprising at least one deuterium atom.

19. A material for an organic electroluminescence device, comprising the compound according to any one of claims 1 to 18.

20. An organic electroluminescence device having a cathode, an anode, and an organic layer between the cathode and the anode, the organic layer including a light-emitting layer, and at least one layer of the organic layer including the compound according to any one of claims 1 to 18.

21. 21. The organic electroluminescent device of claim 20, wherein the organic layer comprises an electron transporting zone between the cathode and the light emitting layer, the electron transporting zone comprising the compound.

22. 22. The organic electroluminescent device of claim 21, wherein the electron transporting zone comprises a first electron transporting layer on the cathode side and a second electron transporting layer on the cathode side, and the first electron transporting layer, the second electron transporting layer, or both contain the compound.

23. 23. The organic electroluminescence device according to claim 21, wherein the electron transporting zone further comprises a cathode-side hole blocking layer, the hole blocking layer comprising the compound.

24. 24. The organic electroluminescent device of claim 23, wherein the hole blocking layer is adjacent to the light emitting layer.

25. The organic electroluminescence device according to any one of claims 20 to 24, wherein the light-emitting layer contains a fluorescent dopant material.

26. The organic electroluminescence device according to any one of claims 20 to 24, wherein the light-emitting layer contains a phosphorescent dopant material.

27. An electronic device comprising the organic electroluminescence element according to any one of claims 20 to 26.

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