JP7040583B2 - Quinoxaline compounds and their uses - Google Patents

Description

The present invention relates to a quinoxaline compound and an organic EL device using the same.

The organic EL element is a surface-emitting element in which an organic thin film is sandwiched between a pair of electrodes, and has features such as thinness and light weight, a high viewing angle, and high-speed response, and is expected to be applied to various display elements. .. Recently, some mobile phone displays and the like have begun to be put into practical use. On the other hand, there is still a problem in the luminous efficiency of the organic EL element, and improvement is required particularly for a light emitting material (light emitting host, light emitting dopant) having a large influence on the light emitting efficiency.

The light emission of the organic EL element is obtained by the recombination of electrons and holes injected from the cathode and the anode inside the light emitting layer. Therefore, the material used for the light emitting layer needs to have a bipolar property capable of receiving both electrons and holes. For example, in an organic EL device using a light emitting layer that cannot transport electrons and holes in a well-balanced manner, excess holes or electrons that do not contribute to light emission are generated, and the luminous efficiency is lowered. Further, the excess holes and electrons induce deterioration of the hole transport layer and the electron transport layer adjacent to the light emitting layer, so that the life of the organic EL device is deteriorated.

Carbazole compounds such as 4,4'-bis (9-carbazolyl) biphenyl and 1,3-bis (9-carbazolyl) benzene are well known as luminescence host materials (see, for example, Non-Patent Documents 1 and 2). ). However, these carbazole compounds are insufficient in terms of bipolarity of transporting electrons and holes in a well-balanced manner, and satisfactory results have not been obtained with respect to the luminous efficiency and lifetime of the organic EL device.

Under such circumstances, a light emitting host material in which a quinoxaline ring and a carbazole ring are combined has been reported (see, for example, Patent Documents 1 to 5). In these compounds, the 2-position and / or 3-position of the quinoxaline ring is substituted with a carbazole ring or a substituent having a carbazole ring, and the quinoxaline ring has a bipolar property. However, there is room for improvement in terms of drive voltage, luminous efficiency, and life as a light emitting host material for an organic EL element.

Applied Physics Letters, 1999, Vol. 75, p. 4 Applied Physics Letters, 2003, Vol. 82, p. 2422

Japanese Unexamined Patent Publication No. 2007-284434 Japanese Unexamined Patent Publication No. 2008-106051 Japanese Unexamined Patent Publication No. 2008-106062 Korean Patent Application Publication No. 10-2014-0071944 Korean Patent Application Publication No. 10-2015-0071624

An object of the present invention is to provide a quinoxaline compound that improves the driving voltage, luminous efficiency, and life of an organic EL device as compared with conventionally known materials. Another object of the present invention is to provide an organic EL device having a low voltage, high luminous efficiency, and long life using the specific quinoxaline compound.

As a result of diligent studies, the present inventors have found a quinoxaline compound represented by the following general formula (1), and have completed the present invention. The quinoxaline compound has a substituent that requires a carbazole skeleton introduced at a specific position on the quinoxaline ring, and has not been reported or suggested in the prior art.

(During the ceremony,
R ¹ and R ² are independently aromatic hydrocarbon groups having 6 to 20 carbon atoms or heteroaromatic groups having 3 to 20 carbon atoms [these groups are independently methyl groups and ethyls, respectively. A substituent selected from the group consisting of a group, a linear, branched or cyclic alkyl group having 3 to 18 carbon atoms, a phenyl group, a biphenyl group, a naphthyl group, a phenanthryl group, a pyridyl group, a cyano group, and a heavy hydrogen atom. It may have one or more groups], represents a methyl group, an ethyl group, a linear, branched or cyclic alkyl group having 3 to 18 carbon atoms, a cyano group, a heavy hydrogen atom, or a hydrogen atom.
R ³ to R ⁵ each independently represent a hydrogen atom, a methyl group, a phenyl group, a naphthyl group, or a biphenyl group.
Z is a substituent represented by any of the following general formulas (2) to (21). )

(In the formula, R ⁶ , R ⁷ , R ⁹ , R ¹⁰ , R ¹² to R ³⁸ , R ⁴⁰ to R ⁴³ , R ⁴⁵ to R ⁴⁸ , R ⁵⁰ to R ⁵³ , and R ⁵⁵ to R ⁶⁶ are independent of each other. Then, it represents a hydrogen atom, a methyl group, a phenyl group, a naphthyl group, or a biphenyl group.
^R8 , ^{R11, R39, R44, R49 , and R54 are} each independently an aromatic hydrocarbon group having 6 to 20 carbon atoms or a heteroaromatic group having 3 to 20 carbon atoms [these]. The groups of are independently methyl group, ethyl group, linear, branched or cyclic alkyl group having 3 to 18 carbon atoms, phenyl group, biphenyl group, naphthyl group, phenanthryl group, pyridyl group, quinolyl group, respectively. It has one or more substituents selected from the group consisting of a pyrimidyl group, a diphenylpyridyl group, a diphenylpyrimidyl group, a diphenyltriazyl group, a dibenzothienyl group, a dibenzofuranyl group, a cyano group, and a heavy hydrogen atom. May be good].
Ar ¹ to Ar ⁶ are independently aromatic hydrocarbon groups having 6 to 20 carbon atoms or heteroaromatic groups having 3 to 20 carbon atoms [these groups are independently methyl groups and ethyls, respectively. Substituent selected from the group consisting of a group, a linear, branched or cyclic alkyl group having 3 to 18 carbon atoms, a phenyl group, a dibenzofuranyl group, a dibenzothienyl group, a 9-carbazolyl group, a cyano group, and a heavy hydrogen atom. It may have one or more groups].
X represents a single bond, an oxygen atom or a sulfur atom. )
That is, the present invention relates to the quinoxaline compound represented by the above general formula (1) and its use.

The quinoxaline compound of the present invention has a bipolar property capable of receiving electrons and holes, although it has a chemical structure that has not been reported or suggested in the prior art. Therefore, the organic EL device having at least one light emitting layer containing the quinoxalin compound of the present invention enables both electron injection and hole injection into the light emitting layer, and recombination of electrons and holes in the light emitting layer. It is suggested that it can be responsible for.

As a result of further studies, the quinoxaline compound of the present invention has a significantly lower drive voltage of the organic EL element and emits light, based on the constituent requirements different from those of the prior art, as compared with the compound of the invention disclosed in the prior art. It had a remarkable effect of significantly improving the efficiency and remarkably improving the life of the element. Such a remarkable and exceptional effect of the present invention cannot be easily predicted from the prior art having different constituent requirements.

Therefore, according to the present invention, it is possible to provide an organic EL element having high brightness and efficiency and excellent life.

Hereinafter, the present invention will be described in detail.

In the quinoxalin compound represented by the general formula (1), R ¹ and R ² are independently aromatic hydrocarbon groups having 6 to 20 carbon atoms or heteroaromatic groups having 3 to 20 carbon atoms [ Each of these groups is independently a methyl group, an ethyl group, a linear, branched or cyclic alkyl group having 3 to 18 carbon atoms, a phenyl group, a biphenyl group, a naphthyl group, a phenanthryl group, a pyridyl group, or a cyano group. , And may have one or more substituents selected from the group consisting of heavy hydrogen atoms], methyl group, ethyl group, linear, branched or cyclic alkyl group with 3 to 18 carbon atoms, cyano group. , A heavy hydrogen atom, or a hydrogen atom.

The aromatic hydrocarbon group having 6 to 20 carbon atoms in R ¹ and R ² can be rephrased as an aromatic hydrocarbon group having 6 to 20 carbon atoms which may be linked or condensed, and can be referred to as the substituent. Is not particularly limited, but for example, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a benzofluorenyl group, a phenanthryl group, a fluoranthenyl group, an anthryl group, a pyrenyl group and the like can be used. Can be mentioned.

The heteroaromatic group having 3 to 20 carbon atoms in R ¹ and R ² can be rephrased as a heteroaromatic group having 3 to 20 carbon atoms which may be linked or condensed, and the substituent can be referred to as a substituent. Although not particularly limited, for example, a heteroaromatic group having at least one oxygen atom, a nitrogen atom, or a sulfur atom and having 3 to 20 carbon atoms can be mentioned, and more preferably, the oxygen atom and the nitrogen atom. , And a heteroaromatic group having 3 to 20 carbon atoms containing at least one atom selected from the group consisting of sulfur atoms on the aromatic ring can be mentioned, and the groups thereof are not particularly limited. For example, pyrrolyl group, thienyl group, furyl group, imidazolyl group, pyrazolyl group, thiazolyl group, isothiazolyl group, oxazolyl group, isooxazolyl group, pyridyl group, pyrimidyl group, pyragil group, 1,3,5-triazyl group, indolyl group. , Benzothienyl group, benzofuranyl group, benzoimidazolyl group, indazolyl group, benzothiazolyl group, benzoisothiazolyl group, 2,1,3-benzothiadiazolyl group, benzoxazolyl group, benzoisoxazolyl group, 2, Examples thereof include 1,3-benzoxadiazolyl group, quinolyl group, isoquinolyl group, quinoxalyl group, quinazolyl group, carbazolyl group, dibenzothienyl group, dibenzofuranyl group, phenoxadinyl group, phenothiazine group, phenazine group, thianthrenyl group and the like. Be done.

The linear, branched, or cyclic alkyl group having 3 to 18 carbon atoms in R ¹ and R ² is not particularly limited, and is, for example, a propyl group, an isopropyl group, an n-butyl group, or a sec-butyl group. , Tert-Butyl group, pentyl group, hexyl group, heptyl group, octyl group, stearyl group, cyclopropyl group, cyclohexyl group and the like.

Specific examples of R ¹ and R ² include a phenyl group, a 4-methylphenyl group, a 3-methylphenyl group, a 2-methylphenyl group, a 4-ethylphenyl group, a 3-ethylphenyl group, and a 2-ethylphenyl group. 4-n-propylphenyl group, 4-isopropylphenyl group, 2-isopropylphenyl group, 4-n-butylphenyl group, 4-isobutylphenyl group, 4-sec-butylphenyl group, 4-tert-butylphenyl group, 4-n-Pentylphenyl group, 4-Isopentylphenyl group, 4-neopentylphenyl group, 4-n-hexylphenyl group, 4-n-octylphenyl group, 4-n-decylphenyl group, 4-n- Dodecylphenyl group, 4-cyclopentylphenyl group, 4-cyclohexylphenyl group, 4-tritylphenyl group, 3-tritylphenyl group, 2,4-dimethylphenyl group, 2,5-dimethylphenyl group, 3,4-dimethylphenyl Group, 3,5-dimethylphenyl group, 2,6-dimethylphenyl group, 2,3,5-trimethylphenyl group, 2,3,6-trimethylphenyl group, 3,4,5-trimethylphenyl group, 4- Cyanophenyl group, 3-cyanophenyl group, 3-cyanophenyl group, 4-biphenyl group, 3-biphenyl group, 2-biphenyl group, 2-methyl-1,1'-biphenyl-4-yl group, 3-methyl -1,1'-biphenyl-4-yl group, 2'-methyl-1,1'-biphenyl-4-yl group, 3'-methyl-1,1'-biphenyl-4-yl group, 4'- Methyl-1,1'-biphenyl-4-yl group, 2,6-dimethyl-1,1'-biphenyl-4-yl group, 2,2'-dimethyl-1,1'-biphenyl-4-yl group , 2,3'-dimethyl-1,1'-biphenyl-4-yl group, 2,4'-dimethyl-1,1'-biphenyl-4-yl group, 3,2'-dimethyl-1,1' -Biphenyl-4-yl group, 2', 3'-dimethyl-1,1'-biphenyl-4-yl group, 2', 4'-dimethyl-1,1'-biphenyl-4-yl group, 2' , 5'-dimethyl-1,1'-biphenyl-4-yl group, 2', 6'-dimethyl-1,1'-biphenyl-4-yl group, 4-phenylbiphenyl group, 2-phenylbiphenyl group, 1-naphthyl group, 2-naphthyl group, 2-methylnaphthalen-1-yl group, 4-methylnaphthalen-1-yl group, 6-methylnaphthalene-2-yl group, 4- (1-naphthyl) phenyl group, 4- (2-Nuff Chill) Phenyl Group, 3- (1-naphthyl) Phenyl Group, 3- (2-naphthyl) Phenyl Group, 3-Methyl-4- (1-naphthyl) Phenyl Group, 3-Methyl-4- (2-naphthyl) Phenyl group, 4- (2-methylnaphthalen-1-yl) phenyl group, 3- (2-methylnaphthalen-1-yl) phenyl group, 4-phenylnaphthalen-1-yl group, 4- (2-methylphenyl) ) Naphthalene-1-yl group, 4- (3-methylphenyl) naphthalene-1-yl group, 4- (4-methylphenyl) naphthalene-1-yl group, 6-phenylnaphthalen-2-yl group, 4- (2-Methylphenyl) naphthalene-2-yl group, 4- (3-methylphenyl) naphthalene-2-yl group, 4- (4-methylphenyl) naphthalene-2-yl group, 2-fluorenyl group, 9, 9-Dimethyl-2-fluorenyl group, 9,9-diethyl-2-fluorenyl group, 9,9-di-n-propyl-2-fluorenyl group, 9,9-di-n-octyl-2-fluorenyl group, 9,9-Diphenyl-2-fluorenyl group, 9,9'-spirobifluorenyl group, 9-phenanthril group, 2-phenanthril group, 4- (9-phenanthril) phenyl group, 3- (9-phenanthril) Phenyl group, 11,11'-dimethylbenzo [a] fluoren-9-yl group, 11,11'-dimethylbenzo [a] fluoren-3-yl group, 11,11'-dimethylbenzo [b] fluoren-9 -Il group, 11,11'-dimethylbenzo [b] fluoren-3-yl group, 11,11'-dimethylbenzo [c] fluoren-9-yl group, 11,11'-dimethylbenzo [c] fluoren- 2-yl group, 3-fluoranthenyl group, 8-fluoranthenyl group, 1-pyrenyl group, 2-pyrenyl group, 2-anthryl group, 9-anthryl group, 4- (9-anthryl) phenyl group, 4 -(10-Phenylanthracene-9-yl) phenyl group, 1-imidazolyl group, 2-phenyl-1-imidazolyl group, 2-phenyl-3,4-dimethyl-1-imidazolyl group, 2,3,4-tri Phenyl-1-imidazolyl group, 2- (2-naphthyl) -3,4-dimethyl-1-imidazolyl group, 2- (2-naphthyl) -3,4-diphenyl-1-imidazolyl group, 1-methyl-2 -Imidazolyl group, 1-ethyl-2-imidazolyl group, 1-phenyl-2-imidazolyl group, 1-methyl-4-phenyl-2-imidazolyl group, 1- Methyl-4,5-dimethyl-2-imidazolyl group, 1-methyl-4,5-diphenyl-2-imidazolyl group, 1-phenyl-4,5-dimethyl-2-imidazolyl group, 1-phenyl-4,5 -Diphenyl-2-imidazolyl group, 1-phenyl-4,5-dibiphenylyl-2-imidazolyl group, 1-methyl-3-pyrazolyl group, 1-phenyl-3-pyrazolyl group, 1-methyl-4-pyrazolyl group, 1-Phenyl-4-pyrazolyl group, 1-methyl-5-pyrazolyl group, 1-phenyl-5-pyrazolyl group, 2-thiazolyl group, 4-thiazolyl group, 5-thiazolyl group, 3-isothiazolyl group, 4-isothiazolyl Group, 5-isothiazolyl group, 2-oxazolyl group, 4-oxazolyl group, 5-oxazolyl group, 3-isooxazolyl group, 4-isoxazolyl group, 5-isooxazolyl group, 2-pyridyl group, 3-methyl-2-pyridyl group , 4-Methyl-2-pyridyl group, 5-methyl-2-pyridyl group, 6-methyl-2-pyridyl group, 3-pyridyl group, 4-methyl-3-pyridyl group, 4-pyridyl group, 2-pyrimidyl Group, 2,2'-bipyridine-3-yl group, 2,2'-bipyridine-4-yl group, 2,2'-bipyridine-5-yl group, 2,3'-bipyridine-3-yl group, 2,3'-bipyridine-4-yl group, 2,3'-bipyridine-5-yl group, 5-pyrimidyl group, pyrazil group, 1,3,5-triazyl group, 4,6-diphenyl-1,3 , 5-Triazine-2-yl group, 1-benzoimidazolyl group, 2-methyl-1-benzoimidazolyl group, 2-phenyl-1-benzoimidazolyl group, 1-methyl-2-benzoimidazolyl group, 1-phenyl-2-benzoimidazolyl group , 1-Methyl-5-benzoimidazolyl group, 1,2-dimethyl-5-benzoimidazolyl group, 1-methyl-2-phenyl-5-benzoimidazolyl group, 1-phenyl-5-benzoimidazolyl group, 1,2-diphenyl-5 -Benzoimidazolyl group, 1-methyl-6-benzoimidazolyl group, 1,2-dimethyl-6-benzoimidazolyl group, 1-methyl-2-phenyl-6-benzoimidazolyl group, 1-phenyl-6-benzoimidazolyl group, 1,2- Diphenyl-6-benzoimidazolyl group, 1-methyl-3-indazolyl group, 1-phenyl-3-indazolyl group, 2-benzothiazolyl group, 4-benzothiazolyl group, 5-benzothiazolyl group, 6-benzothiazoli Lu group, 7-benzothiazolyl group, 3-benzoisothiazolyl group, 4-benzoisothiazolyl group, 5-benzoisothiazolyl group, 6-benzoisothiazolyl group, 7-benzoisothiazolyl group, 2, 1,3-benzothiazol-4-yl group, 2,1,3-benzothiazol-5-yl group, 2-benzoxazolyl group, 4-benzoxazolyl group, 5-benzoxazolyl group, 6-benzoxazolyl group, 7-benzoxazolyl group, 3-benzoisoxazolyl group, 4-benzoisoxazolyl group, 5-benzoisoxazolyl group, 6-benzoisoxazolyl Group, 7-benzoxazozolyl group, 2,1,3-benzoxadiazolyl-4-yl group, 2,1,3-benzoxadiazolyl-5-yl group, 2-quinolyl group, 3- Kinolyl group, 5-quinolyl group, 6-quinolyl group, 1-isoquinolyl group, 4-isoquinolyl group, 5-isoquinolyl group, 2-quinoxalyl group, 3-phenyl-2-quinoxalyl group, 6-quinoxalyl group, 2,3 -Dimethyl-6-quinoxalyl group, 2,3-diphenyl-6-quinoxalyl group, 2-quinazolyl group, 4-quinazolyl group, 2-acridinyl group, 9-acridinyl group, 1,10-phenanthroline-3-yl group, 1,10-Phenantroline-5-yl group, 2-thienyl group, 3-thienyl group, 2-benzothienyl group, 3-benzothienyl group, 2-dibenzothienyl group, 4-dibenzothienyl group, 2-furanyl group, 3-Franyl group, 2-benzofuranyl group, 3-benzofuranyl group, 2-dibenzofuranyl group, 4-dibenzofuranyl group, 9-methylcarbazole-2-yl group, 9-methylcarbazole-3-yl group, 9 -Methylcarbazole-4-yl group, 9-phenylcarbazole-2-yl group, 9-phenylcarbazole-3-yl group, 9-phenylcarbazole-4-yl group, 9-biphenylcarbazole-2-yl group, 9 -Biphenylcarbazole-3-yl group, 9-biphenylcarbazole-4-yl group, 2-thiantolyl group, 10-phenylphenothiazine-3-yl group, 10-phenylphenothiazine-2-yl group, 10-phenylphenoxazine- 3-Il group, 10-phenylphenoxadin-2-yl group, 1-methylindole-2-yl group, 1-phenylindole-2-yl group, 9-phenylcarbazole-4-yl group, 1-methylindole -2-Il group, 1-Feni Ruindole-2-yl group, 4- (2-pyridyl) phenyl group, 4- (3-pyridyl) phenyl group, 4- (4-pyridyl) phenyl group, 3- (2-pyridyl) phenyl group, 3- (3-Pyridyl) phenyl group, 3- (4-pyridyl) phenyl group, 4- (2-phenylimidazol-1-yl) phenyl group, 4- (1-phenylimidazol-2-yl) phenyl group, 4- (2,3,4-triphenylimidazol-1-yl) phenyl group, 4- (1-methyl-4,5-diphenylimidazol-2-yl) phenyl group, 4- (2-methylbenzoimidazole-1-yl) Phenyl group, 4- (2-phenylbenzoimidazole-1-yl) phenyl group, 4- (1-methylbenzoimidazole-2-yl) phenyl group, 4- (2-phenylbenzoimidazole-1-yl) Phenyl group, 3- (2-methylbenzoimidazole-1-yl) phenyl group, 3- (2-phenylbenzoimidazole-1-yl) phenyl group, 3- (1-methylbenzoimidazole-2-yl) phenyl group , 3- (2-Phenylbenzoimidazole-1-yl) phenyl group, 4- (3,5-diphenyltriazine-1-yl) phenyl group, 4- (2-thienyl) phenyl group, 4- (2-furanyl) ) Phenyl group, 5-phenylthiophen-2-yl group, 5-phenylfuran-2-yl group, 4- (5-phenylthiophen-2-yl) phenyl group, 4- (5-phenylfuran-2-yl) ) Phenyl group, 3- (5-phenylthiophen-2-yl) phenyl group, 3- (5-phenylfuran-2-yl) phenyl group, 4- (2-benzothienyl) phenyl group, 4- (3- (3-) Phenyl benzothienyl) phenyl group, 3- (2-benzothienyl) phenyl group, 3- (3-benzothienyl) phenyl group, 4- (2-dibenzothienyl) phenyl group, 4- (4-dibenzothienyl) phenyl group, 3- (2-dibenzothienyl) phenyl group, 3- (4-dibenzothienyl) phenyl group, 4- (2-dibenzofuranyl) phenyl group, 4- (4-dibenzofuranyl) phenyl group, 3- (2) -Dibenzofuranyl) phenyl group, 3- (4-dibenzofuranyl) phenyl group, 5-phenylpyridine-2-yl group, 4-phenylpyridine-2-yl group, 5-phenylpyridine-3-yl group, 4- (9-carbazolyl) phenyl group, 3- (9-carbazolyl) phenyl group, propyl group, isopropyl group, Examples of n-butyl group, sec-butyl group, tert-butyl group, pentyl group, hexyl group, heptyl group, octyl group, stearyl group, cyclopropyl group, cyclohexyl group, cyano group, deuterium atom, hydrogen atom and the like. However, it is not limited to these.

R ¹ and R ² have a high effect of prolonging the life of the organic EL element, and are independently linked or fused with 6 to 14 carbon atoms, or at least an aromatic hydrocarbon group. Heteroaromatic groups with 3 to 12 carbon atoms containing one oxygen atom, nitrogen atom, or sulfur atom [These groups are independently methyl group, phenyl group, biphenyl group, naphthyl group, phenanthryl group, respectively. And may have one or more substituents selected from the group consisting of pyridyl groups], preferably a methyl group or a hydrogen atom, each independently having a phenyl group, a methylphenyl group, a naphthyl group, It is more preferably a biphenyl group, a terphenyl group, a phenanthryl group, a naphthylphenyl group, a phenanthrylphenyl group, a pyridyl group, a pyridylphenyl group, or a hydrogen atom, and each of them is independently a phenyl group, a methylphenyl group, or a naphthyl. More preferably, it is a group, a biphenyl group, or a hydrogen atom.

The aromatic hydrocarbon group having 6 to 14 carbon atoms which may be linked or condensed is not particularly limited, and examples thereof include a phenyl group, a naphthyl group, a biphenyl group, and an anthryl group. Be done.

The heteroaromatic group having 3 to 12 carbon atoms containing at least one oxygen atom, nitrogen atom, or sulfur atom is not particularly limited, but is a pyridyl group, a phenylpyridyl group, a pyridylphenyl group, or a dibenzo. Examples thereof include a furanyl group and a dibenzothienyl group.

R ³ to R ⁵ each independently represent a hydrogen atom, a methyl group, a phenyl group, a naphthyl group, or a biphenyl group. Of these, a hydrogen atom, a methyl group, or a phenyl group is preferable, and a hydrogen atom is more preferable, because each of them has a high effect of extending the life of the organic EL element.

In the quinoxaline compound represented by the general formula (1), Z is represented by any of the following general formulas (2) to (21).

In the general formulas (2) to (21), R ⁶ , R ⁷ , R ⁹ , R ¹⁰ , R ¹² to R ³⁸ , R ⁴⁰ to R ⁴³ , R ⁴⁵ to R ⁴⁸ , R ⁵⁰ to R ⁵³ , and R. ⁵⁵ to R ⁶⁶ each independently represent a hydrogen atom, a methyl group, a phenyl group, a naphthyl group, or a biphenyl group.

R ⁶ , R ⁷ , R ⁹ , R ¹⁰ , R ¹² to R ³⁸ , R ⁴⁰ to R ⁴³ , R ⁴⁵ to R ⁴⁸ , R ⁵⁰ to R ⁵³ , and R ⁵⁵ to R ⁶⁶ have long life of organic EL elements. It is preferable that they are each independently a hydrogen atom, a methyl group, or a phenyl group in terms of excellent chemical conversion effect.

In the general formulas (2) to (21), R ⁸ , R ¹¹ , R ³⁹ , R ⁴⁴ , R ⁴⁹ , and R ⁵⁴ are each independently an aromatic hydrocarbon group having 6 to 20 carbon atoms, or Heteroaromatic groups with 3 to 20 carbon atoms [These groups are each independently a methyl group, an ethyl group, a linear, branched or cyclic alkyl group with 3 to 18 carbon atoms, a phenyl group, a biphenyl group, From the group consisting of naphthyl group, phenanthryl group, pyridyl group, quinolyl group, pyrimidyl group, diphenylpyridyl group, diphenylpyrimidyl group, diphenyltriazyl group, dibenzothienyl group, dibenzofuranyl group, cyano group, and dehydrogen atom. It may have one or more substituents selected].

In R ⁸ , R ¹¹ , R ³⁹ , R ⁴⁴ , R ⁴⁹ , and R ⁵⁴ , the aromatic hydrocarbon group having 6 to 20 carbon atoms has the same definition as that shown in R ¹ and R ² , and is in a preferable range. The same applies to those shown in ^R1 and ^R2 .

^In R8, ^R11 , ^R39 , ^R44 , ^R49 , and ^R54 , the heteroaromatic group having 3 to 20 carbon atoms has the same definition as that shown in ^R1 and ^R2 , and has the same definition as that shown in R1 and R2. Is the same as that shown in R ¹ and R ² .

In R ⁸ , R ¹¹ , R ³⁹ , R ⁴⁴ , R ⁴⁹ , and R ⁵⁴ , linear, branched, or cyclic alkyl groups having 3 to 18 carbon atoms have the same definitions as those shown in R ¹ and R ² . The preferred range is the same as that shown in R ¹ and R ² .

R ⁸ , R ¹¹ , R ³⁹ , R ⁴⁴ , R ⁴⁹ , and R ⁵⁴ are aromatics that may be linked or condensed with 6 to 14 carbon atoms in that they are excellent in the effect of prolonging the life of the organic EL element. Group hydrocarbon group, or heteroaromatic group with 3 to 12 carbon atoms containing at least one oxygen atom, nitrogen atom, or sulfur atom [These groups are independently methyl group, phenyl group, biphenyl group, respectively. , Naftyl group, phenanthryl group, pyridyl group, quinolyl group, pyrimidyl group, diphenylpyridyl group, diphenylpyrimidyl group, diphenyltriazyl group, dibenzothienyl group, dibenzofuranyl group, cyano group, and dehydrogen atom. It may have one or more substituents selected from the above], and each of them independently has a phenyl group, a naphthyl group, a fluorenyl group, a phenanthryl group, a pyridyl group, a pyrimidyl group, a triazil group, and a quinolyl group. , Kinazolyl group, dibenzofuranyl group, or dibenzothienyl group [These groups are independently methyl group, phenyl group, biphenyl group, naphthyl group, phenanthryl group, pyridyl group, quinolyl group, pyrimidyl group, diphenylpyridyl. It may have one or more substituents selected from the group consisting of a group, a diphenylpyrimidyl group, a diphenyltriazyl group, a dibenzothienyl group, a dibenzofuranyl group, a cyano group, and a heavy hydrogen atom]. , Phenyl group, methylphenyl group, naphthyl group, biphenyl group, terphenyl group, dimethylfluorenyl group, phenanthryl group, naphthylphenyl group, phenanthrylphenyl group, pyridyl group, diphenylpyridyl group, diphenyl Pyrimidyl group, diphenyltriazyl group, quinolyl group, quinazolyl group, phenylquinazolyl group, biphenylquinazolyl group, dibenzofuranyl group, dibenzothienyl group, pyridylphenyl group, diphenylpyrimidylphenyl group, diphenyltria More preferably, it is a dibenzofuranylphenyl group, or a dibenzothienylphenyl group.

The above-mentioned aromatic hydrocarbon group having 6 to 14 carbon atoms which may be linked or condensed has the same definition as that shown by R ¹ and R ² , and the preferable range is also shown by R ¹ and R ² . It is the same as the one.

The above-mentioned heteroaromatic group having 3 to 12 carbon atoms containing at least one oxygen atom, nitrogen atom, or sulfur atom has the same definition as that shown in ^R1 and ^R2 , and the preferable range is also ^R1 . And the same as those shown by ^R2 .

In the general formulas (2) to (21), Ar ¹ to Ar ⁶ are independently aromatic hydrocarbon groups having 6 to 20 carbon atoms or heteroaromatic groups having 3 to 20 carbon atoms [these of them. The groups are independently methyl group, ethyl group, linear, branched or cyclic alkyl group having 3 to 18 carbon atoms, phenyl group, dibenzofuranyl group, dibenzothienyl group, 9-carbazolyl group and cyano group. , And may have one or more substituents selected from the group consisting of heavy hydrogen atoms].

In Ar ¹ to Ar ⁶ , the aromatic hydrocarbon group having 6 to 20 carbon atoms has the same definition as that shown in R ¹ and R ² , and the preferable range is the same as that shown in R ¹ and R ² . Is.

In Ar ¹ to Ar ⁶ , the heteroaromatic group having 3 to 20 carbon atoms has the same definition as that shown in R ¹ and R ² , and the preferable range is the same as that shown in R ¹ and R ² . be.

In Ar ¹ to Ar ⁶ , a linear, branched, or cyclic alkyl group having 3 to 18 carbon atoms has the same definition as that shown in R ¹ and R ² , and the preferred range is also R ¹ and R ² . Similar to the one shown.

Ar ¹ to Ar ⁶ are aromatic hydrocarbon groups having 6 to 14 carbon atoms which may be linked or condensed, or at least one oxygen atom and nitrogen atom, in that Ar 1 to Ar 6 are excellent in the effect of extending the life of the organic EL element. , Or a heteroaromatic group with 3 to 12 carbon atoms containing a sulfur atom [These groups are independent, methyl group, ethyl group, linear, branched or cyclic alkyl group with 3 to 18 carbon atoms, respectively. , A phenyl group, a dibenzofuranyl group, a dibenzothienyl group, a 9-carbazolyl group, a cyano group, and one or more substituents selected from the group consisting of a heavy hydrogen atom]. Independently, a phenyl group, a methylphenyl group, a naphthyl group, a biphenyl group, a terphenyl group, a phenanthryl group, a naphthylphenyl group, a dibenzofuranyl group, a dibenzothienyl group, a dibenzofuranylphenyl group, or a dibenzothienylphenyl group [ Each of these groups may independently have a methyl group or an ethyl group], and each of them independently has a phenyl group, a methylphenyl group, a naphthyl group, a biphenyl group, or a terphenyl group. More preferably, it is a group, a phenanthryl group, a naphthylphenyl group, a dibenzofuranyl group, a dibenzothienyl group, a dibenzofuranylphenyl group, or a dibenzothienylphenyl group, and each of them is an independent phenyl group, a methylphenyl group, or a naphthyl group. , Or a biphenyl group is more preferred.

The above-mentioned aromatic hydrocarbon group having 6 to 14 carbon atoms which may be linked or condensed has the same definition as that shown by R ¹ and R ² , and the preferable range is also shown by R ¹ and R ² . It is the same as the one.

The above-mentioned heteroaromatic group having 3 to 12 carbon atoms containing at least one oxygen atom, nitrogen atom, or sulfur atom has the same definition as that shown in ^R1 and ^R2 , and the preferable range is also ^R1 . And the same as those shown by ^R2 .

In the general formulas (2) to (21), X represents a single bond, an oxygen atom or a sulfur atom.

Hereinafter, preferred compounds of the present invention are exemplified, but the present invention is not limited to these compounds.

The quinoxaline compound represented by the general formula (1) can be synthesized, for example, by the following route. The halogenated quinoxaline compound (21) is obtained by the condensation reaction of the halogenated ortho-phenylenediamines (19) and the 1,2-diketones (20). Subsequently, the halogenated quinoxaline compound (21) and the secondary amine compound represented by the general formula (22) are reacted in the presence of a base using a copper catalyst or a palladium catalyst, and the general formula (1) is used. The represented quinoxaline compound can be obtained.

[In the formula, R ¹ to R ⁵ and Z represent the same definition as the general formula (1). A represents a halogen atom (iodine, bromine, chlorine, or fluorine). ]
As the compounds represented by the general formulas (19), (20) and (22), commercially available compounds can be used, or they can be synthesized based on generally known methods.

The quinoxaline compound represented by the general formula (1) of the present invention can be preferably used as a light emitting host material, a light emitting dopant material, an electron transporting material, and a hole transporting material for an organic EL device. The quinoxaline compound represented by the general formula (1) of the present invention has bipolarity, can stably transport holes and electrons, and is also excellent in light emission characteristics. When used as a light emitting layer, it is possible to realize high efficiency and long life of the organic EL element.

When the quinoxaline compound represented by the general formula (1) of the present invention is used as a light emitting layer of an organic EL device, the quinoxaline compound is used alone, doped with a known light emitting host material, or known. It can be used by doping with a light emitting dopant.

When the quinoxaline compound represented by the general formula (1) is used as a hole transport layer or an electron transport layer of an organic EL element, a conventionally known fluorescent or phosphorescent light emitting material is used as the light emitting layer. can do. The light emitting layer may be formed of only one kind of light emitting material, or may be doped with one or more kinds of light emitting materials in the host material.

As a method for forming the light emitting layer, the hole transport layer or the electron transport layer containing the quinoxaline compound represented by the general formula (1), for example, a known method such as a vacuum vapor deposition method, a spin coating method, a casting method or the like. Can be applied.

The basic structure of the organic EL device to which the effect of the present invention can be obtained preferably includes a substrate, an anode, a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, and a cathode, and some of them are included. Layers may be omitted or vice versa.

The anode and cathode of the organic EL element are connected to the power supply via an electric conductor. By applying a potential between the anode and the cathode, the organic EL element operates.

Holes are injected into the organic EL device from the anode, and electrons are injected into the organic EL device at the cathode.

The organic EL element is typically overlaid on the substrate and the anode or cathode can be in contact with the substrate. The electrodes that come into contact with the substrate are called lower electrodes for convenience. Generally, the lower electrode is an anode, but the organic EL device of the present invention is not limited to such a form.

The substrate may be light transmissive or opaque, depending on the intended emission direction. The light transmission characteristics can be confirmed by electroluminescence emission through the substrate. Generally, transparent glass or plastic is adopted as the substrate in such a case. The substrate may have a composite structure including multiple material layers.

When electroluminescence emission is confirmed through an anode, the anode is formed by passing or substantially passing the emission.

The general transparent anode material used in the present invention is not particularly limited, and examples thereof include indium-tin oxide (ITO), indium-zinc oxide (IZO), and tin oxide. .. Other metal oxides such as aluminum or indium-doped tin oxide, magnesium-indium oxide, or nickel-tungsten oxide can also be used. In addition to these oxides, metal nitrides such as gallium nitride, metal seleniums such as zinc selenide, or metal sulfides such as zinc sulfide can be used as the anode.

The anode can be modified with plasma-deposited fluorocarbons. If electroluminescence emission is confirmed only through the cathode, the transmission properties of the anode are not important and any transparent, opaque or reflective conductive material can be used. Examples of conductors for this application include gold, iridium, molybdenum, palladium, platinum and the like.

A plurality of hole-transporting layers such as a hole-injecting layer and a hole-transporting layer can be provided between the anode and the light-emitting layer. The hole injection layer and the hole transport layer have a function of transmitting holes injected from the anode to the light emitting layer, and by interposing these layers between the anode and the light emitting layer, many holes are generated at a lower electric field. Holes can be injected into the light emitting layer.

In the organic EL device of the present invention, known hole injection materials and hole transport materials can be used as the hole transport layer and / or the hole injection layer. For example, triazole derivative, oxadiazole derivative, imidazole derivative, polyarylalkane derivative, pyrazoline derivative and pyrazolone derivative, phenylenediamine derivative, arylamine derivative, amino-substituted carcon derivative, oxazole derivative, styrylanthracene derivative, fluorenone derivative, hydrazone derivative, stilben. Examples thereof include derivatives, silazane derivatives, aniline-based copolymers, and conductive polymer oligomers, particularly thiophene oligomers. As the hole injecting material and the hole transporting material, the above-mentioned ones can be used, but porphyrin compounds, aromatic tertiary amine compounds and styrylamine compounds, particularly aromatic tertiary amine compounds may be used. preferable.

Typical examples of the above aromatic tertiary amine compound and styrylamine compound are N, N, N', N'-tetraphenyl-4,4'-diaminophenyl, N, N'-diphenyl-N, N'. -Bis (3-methylphenyl)-[1,1'-biphenyl] -4,4'-diamine (TPD), 2,2-bis (4-di-p-tolylaminophenyl) propane, 1,1- Bis (4-di-p-tolylaminophenyl) cyclohexane, N, N, N', N'-tetra-p-tolyl-4,4'-diaminobiphenyl, 1,1-bis (4-di-p-) Trillaminophenyl) -4-phenylcyclohexane, bis (4-dimethylamino-2-methylphenyl) phenylmethane, bis (4-di-p-tolylaminophenyl) phenylmethane, N, N'-diphenyl-N, N '-Di (4-methoxyphenyl) -4,4'-diaminobiphenyl, N, N, N', N'-tetraphenyl-4,4'-diaminodiphenyl ether, 4,4'-bis (diphenylamino) Audriphenyl, N, N, N-tri (p-tolyl) amine, 4- (di-p-tolylamino) -4'-[4- (di-p-tolylamino) styryl] stilben, 4-N, N- Diphenylamino- (2-diphenylvinyl) benzene, 3-methoxy-4'-N, N-diphenylaminostillbenzene, N-phenylcarbazole, 4,4'-bis [N- (1-naphthyl) -N-phenyl Examples thereof include amino] biphenyl (NPD), 4,4', 4''-tris [N- (3-methylphenyl) -N-phenylamino] triphenylamine (MTDATA).

Inorganic compounds such as p-type-Si and p-type-SiC can also be used as hole injection materials and hole transport materials. The hole injection layer and the hole transport layer may have a one-layer structure composed of one or more of the above materials, or may have a laminated structure composed of a plurality of layers having the same composition or different compositions.

In the organic EL device of the present invention, the light emitting layer contains the quinoxaline compound of the present invention. For the light emitting layer, a known light emitting material (light emitting host material, fluorescent dopant, phosphorescent dopant) can be selected and used in combination with the quinoxaline compound of the present invention.

Examples of the light emitting host material include compounds having a biphenyl group, a fluorenyl group, a triphenylsilyl group, a carbazole group, a pyrenyl group, or an anthranyl group. For example, DPVBi (4,4'-bis (2,2-diphenylvinyl) -1,1'-biphenyl), BCzVBi (4,4'-bis (9-ethyl-3-carbazobinylene) 1,1'-biphenyl. ), TBADN (2-talshalbutyl-9,10-di (2-naphthyl) anthracene), ADN (9,10-di (2-naphthyl) anthracene), CBP (4,4'-bis (carbazole-9) -Il) biphenyl), CDBP (4,4'-bis (carbazole-9-yl) -2,2'-dimethylbiphenyl), 9,10-bis (biphenyl) anthracene and the like.

Examples of fluorescent dopants include anthracene, tetracene, xanthene, perylene, rubrene, coumarin, rhodamine, quinacridone, dicyanomethylenepyrine compound, thiopyran compound, polymethine compound, pyrylium or thiapyrylium compound, fluorene derivative, perifurantene derivative, indenoperylene derivative, Examples thereof include bis (azinyl) amine boron compounds, bis (azinyl) methane compounds, and carbostylyl compounds.

Examples of phosphorescent dopants include organic metal complexes of transition metals such as iridium, platinum, palladium and osmium.

Examples of dopants are Alq ₃ (tris (8-hydroxyquinoline) aluminum), DPAVBi (4,4'-bis [4- (di-para-tolylamino) styryl] biphenyl), perylene, Ir (PPy) ₃ ( Examples thereof include tris (2-phenylpyridine) iridium (III), FlrPic (bis (3,5-difluoro-2- (2-pyridyl) phenyl- (2-carboxypyridyl) iridium (III)), and the like.

Examples of the electron transporting material include an alkali metal complex, an alkaline earth metal complex, and an earth metal complex. Examples of the alkali metal complex, alkaline earth metal complex, or earth metal complex include 8-hydroxyquinolinate lithium (Liq), bis (8-hydroxyquinolinate) zinc, and bis (8-hydroxyquinolinate). Copper, bis (8-hydroxyquinolinate) manganese, tris (8-hydroxyquinolinate) aluminum, tris (2-methyl-8-hydroxyquinolinate) aluminum, tris (8-hydroxyquinolinate) gallium, Bis (10-hydroxybenzo [h] quinolinate) berylium, bis (10-hydroxybenzo [h] quinolinate) zinc, bis (2-methyl-8-quinolinate) chlorogallium, bis (2-methyl-8-quinolinate) ( Examples thereof include o-cresolate) gallium, bis (2-methyl-8-quinolinate) -1-naphtholate aluminum, and bis (2-methyl-8-quinolinate) -2-naphtholate gallium.

A hole blocking layer may be provided between the light emitting layer and the electron transport layer for the purpose of improving the carrier balance. Desirable compounds for the hole element layer are BCP (2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline), Bphenyl (4,7-diphenyl-1,10-phenanthroline), BAlq (bis (2). -Methyl-8-quinolinolate) -4- (phenylphenanthroline) aluminum), bis (10-hydroxybenzo [h] quinolinate) beryllium) and the like can be mentioned.

In the organic EL device of the present invention, an electron injection layer may be provided for the purpose of improving the electron injection property and improving the device characteristics (for example, luminous efficiency, constant voltage drive, or high durability).

Desirable compounds for the electron injection layer include fluorenone, anthraquinodimethane, diphenoquinone, thiopyrandioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, fleolenilidenemethane, anthraquinodimethane, anthron and the like. Can be mentioned. In addition, the above-mentioned metal complexes, alkali metal oxides, alkaline earth oxides, rare earth oxides, alkali metal halides, alkaline earth halides, rare earth halides, SiO ₂ , AlO, SiN, SiON, AlON, Various oxides such as GeO, LiO, LiON, TIO, TiON, TaO, TaON, TaN, and C, nitrides, and inorganic compounds such as oxide nitrides can also be used.

The cathode used in the present invention can be formed from any conductive material if the emission is confirmed only through the anode. Desirable cathode materials include sodium, sodium-potassium alloy, magnesium, lithium, magnesium / copper mixture, magnesium / silver mixture, magnesium / aluminum mixture, magnesium / indium mixture, aluminum / aluminum oxide (Al ₂ O ₃ ) mixture, indium. , Lithium / aluminum mixture, rare earth metals and the like.

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

^{1 1} H-NMR and ¹³ C-NMR measurements were carried out using Gemini 200 manufactured by Varian.

The FDMS measurement was performed using M-80B manufactured by Hitachi, Ltd.

Synthesis Example 1 (Synthesis of 2-chloro-9- (2,3-diphenylquinoxaline-6-yl) carbazole)

2-Chlorocarbazole 0.6 g (3.0 mmol), 6-bromo-2,3-diphenylquinoxaline 1.0 g (3.0 mmol), potassium carbonate 0.6 g (4.) in a 30 mL three-necked flask under a nitrogen stream. 5 mmol), 10 mL of o-xylene, 6 mg (0.03 mmol) of palladium acetate, and 20 mg (0.1 mmol) of tri (tert-butyl) phosphine were added and stirred at 130 ° C. for 8 hours. After cooling to room temperature, 10 mL of pure water and 10 mL of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 1.2 g (2.5 mmol) of yellow powder of 2-chloro-9- (2,3-diphenylquinoxaline-6-yl) carbazole was simply added. Separated (yield 85%).

The compounds were identified by ¹ H-NMR measurement and ¹³ C-NMR measurement.

^{1 1} H-NMR (CDCl ₃ ) δ (ppm); 8.36-8.39 (m, 2H), 8.02-8.11 (m, 2H), 7.94 (d, 1H), 7. 27-7.55 (m, 15H)
¹³ C-NMR (CDCl ₃ ) δ (ppm); 154.81, 154.32, 142.20, 141.30, 141.10, 140.53, 139.08, 139.02, 138.64, 132 .36, 131.45, 130.17, 129.45, 129.38, 129.00, 128.67, 126.83, 126.21, 123.53, 122.70, 121.59, 121.44 , 121.38, 120.72, 110.27
Synthesis Example 2 (Synthesis of 4-chloro-9- (2,3-diphenylquinoxaline-6-yl) carbazole)

4-Chlorocarbazole 0.6 g (3.0 mmol), 6-bromo-2,3-diphenylquinoxaline 1.0 g (3.0 mmol), potassium carbonate 0.6 g (4.) in a 30 mL three-necked flask under a nitrogen stream. 5 mmol), 10 mL of o-xylene, 6 mg (0.03 mmol) of palladium acetate, and 20 mg (0.1 mmol) of tri (tert-butyl) phosphine were added and stirred at 130 ° C. for 8 hours. After cooling to room temperature, 10 mL of pure water and 10 mL of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 1.1 g (2.4 mmol) of yellow powder of 4-chloro-9- (2,3-diphenylquinoxaline-6-yl) carbazole was simply added. Separated (yield 81%).

The compounds were identified by ¹ H-NMR measurement and ¹³ C-NMR measurement.

^{1 1} H-NMR (CDCl ₃ ) δ (ppm); 8.70 (d, 1H), 8.35-8.38 (m, 2H), 7.92 (d, 1H), 7.28-7. 56 (m, 16H)
¹³ C-NMR (CDCl ₃ ) δ (ppm); 154.77, 154.35, 142.15, 141.95, 140.96, 140.59, 139.08, 139.02, 138.72, 131 .36, 130.17, 129.46, 129.40, 129.33, 129.28, 128.68, 127.07, 126.70, 123.62, 123.03, 121.74, 121.35 , 121.27, 109.89, 108.46
Example 1 (Synthesis of compound (D5))

In a 30 mL three-necked flask under a nitrogen stream, 1.0 g (2.0 mmol) of 2-chloro-9- (2,3-diphenylquinoxalin-6-yl) carbazole obtained in Synthesis Example 1, N, N-bis ( 4-biphenyl) amine 0.64 g (2.0 mmol), sodium-tert-butoxide 0.27 g (2.8 mmol), o-xylene 10 mL, palladium acetate 4 mg (0.02 mmol), and tri (tert-butyl) phosphine. 14 mg (0.07 mmol) was added and the mixture was stirred at 140 ° C. for 8 hours. After cooling to room temperature, 10 mL of pure water and 10 ml of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 1.4 g (1.8 mmol) of the yellow powder of compound (D5) was isolated (yield 91%).

Compounds were identified by FDMS, ¹ H-NMR measurement, and ¹³ C-NMR measurement.

FDMS (m / z); 766 (M +)
^{1 1} H-NMR (CDCl ₃ ) δ (ppm); 8.24-8.33 (m, 2H), 8.02-8.06 (m, 2H), 7.90 (d, 1H), 7. 13-7.54 (m, 33H)
¹³ C-NMR (CDCl ₃ ) δ (ppm); 154.63, 154.07, 147.54, 146.67, 142.25, 141.84, 141.33, 140.85, 140.43, 139 .15, 139.06,135.44, 131.25, 130.14, 129.31, 129.26, 129.14, 129.06, 128.61, 128.08, 127.11, 126.91 , 126.08, 125.97, 124.20, 124.11, 121.58, 121.22, 120.38, 120.28, 119.55, 110.01, 106.74
Example 2 (Synthesis of compound (F5))

In a 30 mL three-necked flask under a nitrogen stream, 1.0 g (2.0 mmol) of 4-chloro-9- (2,3-diphenylquinoxalin-6-yl) carbazole obtained in Synthesis Example 2, N, N-bis ( 4-biphenyl) amine 0.64 g (2.0 mmol), sodium-tert-butoxide 0.27 g (2.8 mmol), o-xylene 10 mL, palladium acetate 4 mg (0.02 mmol), and tri (tert-butyl) phosphine. 14 mg (0.07 mmol) was added and the mixture was stirred at 140 ° C. for 8 hours. After cooling to room temperature, 10 mL of pure water and 10 ml of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 1.3 g (1.7 mmol) of the yellow powder of compound (F5) was isolated (yield 88%).

Compounds were identified by FDMS, ¹ H-NMR measurement, and ¹³ C-NMR measurement.

FDMS (m / z); 766 (M +)
^{1 1} H-NMR (CDCl ₃ ) δ (ppm); 8.39-8.47 (m, 2H), 8.04 (d, 1H), 7.92 (d, 1H), 7.22-7. 56 (m, 32H), 7.06-7.16 (m, 2H)
¹³ C-NMR (CDCl ₃ ) δ (ppm); 154.72, 154.23, 146.96, 142.64, 142.25, 141.49, 140.97, 140.79, 140.52, 139 .12, 139.08, 134.90, 131.23, 130.16, 129.52, 129.42, 129.35, 128.99, 128.67, 128.13, 127.53, 126.97 , 126.88, 126.58, 126.44, 123.59, 122.33, 121.49, 121.22, 109.61, 107.88
Example 3 (Synthesis of compound (B4))

6-bromo-2,3-diphenylquinoxaline 2.8 g (7.8 mmol), 9-biphenylcarbazole-2-boronic acid 3.0 g (8.2 mmol), tetrakis (triphenyl) in a 50 mL three-necked flask under a nitrogen stream. Hosphin) 0.27 g (0.24 mmol) of palladium, 10 mL of tetrahydrofuran, and 10 g of a 20 wt% sodium carbonate aqueous solution (19.6 mmol as sodium carbonate) were added, and the mixture was heated under reflux for 7 hours. After cooling to room temperature, the aqueous layer and the organic layer were separated, and the organic layer was washed with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium chloride. After drying over anhydrous magnesium sulfate, the mixture was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane) to isolate 4.2 g (7.0 mmol) of a pale yellow solid of compound (B4) (yield 89%).

Compound identification was performed by FDMS measurement.

FDMS (m / z); 599 (M +)
Example 4 (Synthesis of compound (C18))

6-bromo-2,3-dibiphenylquinoxaline 5.1 g (10.0 mmol), 9-phenylcarbazole-3-boronic acid 3.0 g (10.5 mmol), tetrakis (tri) in a 50 mL three-necked flask under a nitrogen stream. (Phenylphosphin) 0.35 g (0.30 mmol) of palladium, 13 mL of tetrahydrofuran, and 13.3 g (25.2 mmol as sodium carbonate) of a 20 wt% sodium carbonate aqueous solution were added, and the mixture was heated under reflux for 6 hours. After cooling to room temperature, the aqueous layer and the organic layer were separated, and the organic layer was washed with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium chloride. After drying over anhydrous magnesium sulfate, the mixture was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane) to isolate 6.2 g (9.1 mmol) of a pale yellow solid of compound (C18) (yield 91%).

Compound identification was performed by FDMS measurement.

FDMS (m / z); 675 (M +)
Example 5 (Synthesis of compound (D16))

2.5 g (5.1 mmol) of 2-chloro-9- (2,3-diphenylquinoxaline-6-yl) carbazole obtained in Synthesis Example 1 and 0.95 g of phenoxazine in a 30 mL three-necked flask under a nitrogen stream. 5.1 mmol), sodium-tert-butoxide 0.75 g (7.7 mmol), o-xylene 12 mL, palladium acetate 10 mg (0.05 mmol), and tri (tert-butyl) phosphine 30 mg (0.16 mmol). The mixture was stirred at 140 ° C. for 5 hours. After cooling to room temperature, 10 mL of pure water and 10 mL of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 2.8 g (4.4 mmol) of a yellow solid of compound (D16) was isolated (yield 86%).

FDMS (m / z); 628 (M +)
Example 6 (Synthesis of compound (E13))

In a 30 mL three-necked flask under a nitrogen stream, 2.3 g (6.3 mmol) of 6-bromo-2,3-diphenylquinoxaline, 2.1 g (6.3 mmol) of 3,9-bicarbazole, and 1.3 g of potassium carbonate ( 9.5 mmol), 11 mL of o-xylene, 14 mg (0.06 mmol) of palladium acetate, and 38 mg (0.19 mmol) of tri (tert-butyl) phosphine were added and stirred at 140 ° C. for 8 hours. After cooling to room temperature, 10 mL of pure water and 10 mL of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 3.5 g (5.7 mmol) of a yellow solid of compound (E13) was isolated (yield 90%).

Compounds were identified by FDMS, ¹ H-NMR measurement, and ¹³ C-NMR measurement.

FDMS (m / z); 612 (M +)
^{1 1} H-NMR (CDCl ₃ ) δ (ppm); 8.51 (s, 1H), 8.42 (d, 1H), 8.33 (s, 1H), 8.09-8.20 (m, 4H), 7.80 (d, 1H), 7.67 (d, 1H), 7.49-7.60 (m, 6H), 7.27-7.43 (m, 13H)
¹³ C-NMR (CDCl ₃ ) δ (ppm); 154.53, 154.01, 141.96, 141.79, 141.17, 140.23, 139.55, 138.80, 138.75, 138 .68, 131.13, 130.58, 129.86, 129.15, 129.08, 128.82, 128.38, 126.98, 125.94, 125.89, 125.75, 124.95 , 123.41, 123.15, 121.08, 120.74, 120.28, 119.66, 119.61, 110.96, 110.19, 109.77
Example 7 (Synthesis of compound (G1))

In a 30 mL three-necked flask under a nitrogen stream, 3.1 g (8.7 mmol) of 6-bromo-2,3-diphenylquinoxaline, 2.9 g (8.7 mmol) of benzo [a] carbazole, and 1.8 g (13) of potassium carbonate. .1 mmol), o-xylene 16 mL, palladium acetate 20 mg (0.09 mmol), and tri (tert-butyl) phosphine 53 mg (0.26 mmol) were added and stirred at 140 ° C. for 8 hours. After cooling to room temperature, 10 mL of pure water and 10 mL of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 3.8 g (7.6 mmol) of a yellow solid of compound (G1) was isolated (yield 87%).

Compounds were identified by FDMS, ¹ H-NMR measurement, and ¹³ C-NMR measurement.

FDMS (m / z); 497 (M +)
^{1 1} H-NMR (CDCl ₃ ) δ (ppm); 8.49 (s, 1H), 8.38 (d, 1H), 8.21-8.28 (m, 2H), 8.01 (d, 1H), 7.77-7.81 (m, 2H), 7.53-7.63 (m, 5H), 7.33-7.45 (m, 10H), 7.19 (t, 1H)
¹³ C-NMR (CDCl ₃ ) δ (ppm); 154.51, 154.30, 141.90, 141.69, 141.36, 140.76, 138.80, 138.67, 135.31, 133 .52, 131.05, 130.95, 129.89, 129.88, 129.26, 129.19, 129.16, 128.40, 128.36, 128.29, 125.31, 125.20 , 124.86, 123.89, 122.35, 121.69, 121.88, 120.88, 120.31, 119.68, 119.03, 110.29
Example 8 (Synthesis of compound (H1))

In a 30 mL three-necked flask under a nitrogen stream, 2.6 g (7.3 mmol) of 6-bromo-2,3-diphenylquinoxaline, 1.6 g (7.3 mmol) of benzo [b] carbazole, and 1.5 g (10) of potassium carbonate. .9 mmol), 13 mL of o-xylene, 16 mg (0.16 mmol) of palladium acetate, and 44 mg (0.22 mmol) of tri (tert-butyl) phosphine were added and stirred at 140 ° C. for 10 hours. After cooling to room temperature, 10 mL of pure water and 10 mL of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 3.2 g (6.4 mmol) of a yellow solid of compound (H1) was isolated (yield 88%).

Compound identification was performed by FDMS and ¹ H-NMR measurement.

FDMS (m / z); 497 (M +)
^{1 1} H-NMR (CDCl ₃ ) δ (ppm); 8.64 (s, 1H), 8.51 (s, 1H), 8.44 (d, 1H), 8.30 (d, 1H), 8 .10 (t, 2H), 7.94 (s, 1H), 7.87 (d, 1H), 7.35-7.58 (m, 15H)
Example 9 (Synthesis of compound (J5))

In a 30 mL three-necked flask under a nitrogen stream, 2.3 g (5.1 mmol) of 6-bromo-2,3-di (1-naphthyl) quinoxaline, 1.1 g (5.1 mmol) of benzo [c] carbazole, and potassium carbonate. 1.0 g (7.6 mmol), 11 mL of o-xylene, 11 mg (0.05 mmol) of palladium acetate, and 31 mg (0.15 mmol) of tri (tert-butyl) phosphine were added and stirred at 140 ° C. for 10 hours. After cooling to room temperature, 10 mL of pure water and 10 mL of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 2.6 g (4.3 mmol) of a yellow solid of compound (J5) was isolated (yield 85%).

Compound identification was performed by FDMS measurement.

FDMS (m / z); 597 (M +)
Example 10 (Synthesis of compound (K1))

In a 30 mL three-necked flask under a nitrogen stream, 1.3 g (3.6 mmol) of 6-bromo-2,3-diphenylquinoxaline, 0.99 g (3.6 mmol) of dibenzo [a, c] carbazole, 0.77 g of potassium carbonate. (5.5 mmol), 7 mL of o-xylene, 8 mg (0.04 mmol) of palladium acetate, and 22 mg (0.11 mmol) of tri (tert-butyl) phosphine were added and stirred at 140 ° C. for 7 hours. After cooling to room temperature, 10 mL of pure water and 10 mL of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 1.8 g (3.3 mmol) of a yellow solid of compound (K1) was isolated (yield 89%).

Compound identification was performed by FDMS measurement.

FDMS (m / z); 547 (M +)
Example 11 (Synthesis of compound (N6))

In a 30 mL three-necked flask under a nitrogen stream, 1.3 g (3.6 mmol) of 6-bromo-2,3-di (2-naphthyl) quinoxaline, 1.1 g (4.3 mmol) of dibenzo [a, g] carbazole, Potassium carbonate 0.90 g (6.5 mmol), o-xylene 10 mL, palladium acetate 10 mg (0.04 mmol), and tri (tert-butyl) phosphine 26 mg (0.13 mmol) were added and stirred at 140 ° C. for 9 hours. .. After cooling to room temperature, 10 mL of pure water and 10 mL of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 2.4 g (4.0 mmol) of a yellow solid of compound (N6) was isolated (yield 92%).

Compound identification was performed by FDMS measurement.

FDMS (m / z); 597 (M +)
Example 12 (Synthesis of compound (P1))

2-Chloro-9- (2,3-diphenylquinoxalin-6-yl) carbazole obtained in Synthesis Example 1 in a 30 mL three-necked flask under a nitrogen stream, 3.4 g (7.1 mmol), 9-phenylcarbazole-2- Boronic acid 2.1 g (7.5 mmol), palladium acetate 32 mg (0.14 mmol), 2-dicyclohexylphosphino-2'4'6'-triisopropylbiphenyl 137 mg, tetrahydrofuran 12 mL, and 20 wt% potassium carbonate aqueous solution 12. 3 g (17.9 mmol as potassium carbonate) was added, and the mixture was heated under reflux for 10 hours. After cooling to room temperature, the aqueous layer and the organic layer were separated, and the organic layer was washed with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium chloride. After drying over anhydrous magnesium sulfate, the mixture was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane) to isolate 4.2 g (6.1 mmol) of a pale yellow solid of compound (P1) (yield 85%).

Compound identification was performed by FDMS measurement.

FDMS (m / z); 688 (M +)
Example 13 (Synthesis of compound (Q1))

2-Chloro-9- (2,3-diphenylquinoxalin-6-yl) carbazole obtained in Synthesis Example 1 in a 30 mL three-necked flask under a nitrogen stream 4.1 g (8.6 mmol), 9-phenylcarbazole-3- 126 g (9.0 mmol) of boronic acid, 39 mg (0.17 mmol) of palladium acetate, 165 mg of 2-dicyclohexylphosphino-2'4'6'-triisopropylbiphenyl, 15 mL of tetrahydrofuran, and 20 wt% potassium carbonate aqueous solution 14. 9 g (21.6 mmol as potassium carbonate) was added, and the mixture was heated under reflux for 9 hours. After cooling to room temperature, the aqueous layer and the organic layer were separated, and the organic layer was washed with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium chloride. After drying over anhydrous magnesium sulfate, the mixture was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane) to isolate 5.3 g (7.6 mmol) of a pale yellow solid of compound (Q1) (yield 89%).

Compounds were identified by FDMS, ¹ H-NMR measurement, and ¹³ C-NMR measurement.

FDMS (m / z); 688 (M +)
^{1 1} H-NMR (CDCl ₃ ) δ (ppm); 8.48 (s, 1H), 8.38-8.43 (m, 2H), 8.16-8.28 (m, 3H), 8. 08 (d, 1H), 7.85 (s, 1H), 7.71 (t, 2H), 7.55-7.61 (m, 9H), 7.34-7.46 (m, 13H)
¹³ C-NMR (CDCl ₃ ) δ (ppm); 154.37, 153.83, 142.06, 141.35, 141.26, 141.02, 140.77, 140.33, 140.19, 139 .07, 138.90, 138.81, 137.64, 134.04, 130.99, 129.88, 129.22, 129.05, 128.99, 128.33, 128.35, 127.48 , 127.05, 126.08, 125.93, 123.89, 123.79, 123.45122.51,120.75,120.44,120.00, 119.21,109.99,109.87 , 109.81, 108.34
Example 14 (Synthesis of compound (R4))

2.3 g (4.9 mmol) of 3-chloro-9- (2,3-diphenylquinoxalin-6-yl) carbazole and 1.8 g of 9-biphenylcarbazole-2-boronic acid in a 30 mL three-mouthed flask under a nitrogen stream. 5.1 mmol), palladium acetate 22 mg (0.10 mmol), 2-dicyclohexylphosphino-2'4'6'-triisopropylbiphenyl 94 mg, tetrahydrofuran 10 mL, and 20 wt% potassium carbonate aqueous solution 8.4 g (12 as potassium carbonate) .2 mmol) was added, and the mixture was heated under reflux for 12 hours. After cooling to room temperature, the aqueous layer and the organic layer were separated, and the organic layer was washed with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium chloride. After drying over anhydrous magnesium sulfate, the mixture was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane) to isolate 3.3 g (4.3 mmol) of a pale yellow solid of compound (R4) (yield 88%).

Compound identification was performed by FDMS measurement.

FDMS (m / z); 764 (M +)

Example 15 (Synthesis of compound (S1))

6-bromo-2,3-diphenylquinoxaline 2.8 g (7.7 mmol), 3- (9-phenylcarbazole-3-yl) carbazole 3.1 g (7.7 mmol) in a 30 mL three-necked flask under a nitrogen stream. , Potassium carbonate 1.6 g (11.6 mmol), o-xylene 15 mL, palladium acetate 17 mg (0.08 mmol), and tri (tert-butyl) phosphine 47 mg (0.23 mmol) were added and stirred at 140 ° C. for 10 hours. did. After cooling to room temperature, 10 mL of pure water and 10 ml of tetrahydrofuran were added, and the organic layer was separated. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mixed solvent of toluene and hexane), and 4.8 g (6.9 mmol) of a yellow solid of compound (S1) was isolated (yield 90%).

Compounds were identified by FDMS, ¹ H-NMR measurement, and ¹³ C-NMR measurement.

FDMS (m / z); 688 (M +)
^{1 1} H-NMR (CDCl ₃ ) δ (ppm); 8.41-8.49 (m, 4H), 8.27 (t, 2H), 8.10 (d, 1H), 7.81 (t, 2H), 732-7.73 (m, 23H)
¹³ C-NMR (CDCl ₃ ) δ (ppm); 142.02, 141.37, 140.89, 140.11, 139.55, 139.12, 138.89, 138.84, 137.76, 135 .14, 134.12, 130.92, 129.90, 129.87, 129.08, 129.00, 128.91, 128.37, 127.46, 127.08, 126.38, 126.10 , 125.80, 125.59, 124.52, 124.11, 123.99, 123.54, 120.76, 120.59, 120.43, 120.00, 119.03, 118.91, 110 .11, 110.05, 109.89
Example 16 (Evaluation of element of compound (D5))
A glass substrate on which an ITO transparent electrode (anolyde) having a thickness of 200 nm was laminated was ultrasonically cleaned with acetone and pure water, and boiled with isopropyl alcohol. After further cleaning with ultraviolet ozone and installing in a vacuum vapor deposition apparatus, the gas was exhausted with a vacuum pump until it became 1 × 10 ^-4 Pa. First, 4,4'-bis [N- (9-phenylcarbazole-3-yl) -N-phenyl] biphenyl was deposited on an ITO transparent electrode at a vapor deposition rate of 0.3 nm / sec, and a hole injection layer of 65 nm was deposited. And said. Subsequently, 4,4'-bis [N- (1-naphthyl) -N-phenyl] biphenyl (NPD) was deposited at a vapor deposition rate of 0.3 nm / sec at 10 nm to form a hole transport layer. Subsequently, bis- (1-phenylisoquinolyl) iridium (III) acetylacetonate ((piq) ₂ Ir (acac)) was used as the light-emitting dopant material, and compound (D5) was used as the host material in a weight ratio of 8:92. The vapor deposition was carried out at a vapor deposition rate of 0.25 nm / sec so as to obtain a light emitting layer having a vapor deposition rate of 40 nm. Next, the vapor deposition rate of 9,10-di (1-naphthyl) -2- (4-phenyl-1-phenyl-1H-benzo [d] imidazole) and lithium quinolinol was 0 so that the weight ratio was 50:50. Co-deposited at .15 nm / sec to form a 30 nm electron transport layer. Further, silver and magnesium were co-deposited at a vapor deposition rate of 0.5 nm / sec to 80 nm so that the weight ratio was 1:10 to form a cathode. Under a nitrogen atmosphere, a glass plate for sealing was adhered with a UV curable resin to obtain an organic EL element for evaluation. A current of 20 mA / cm ² was applied to the device thus manufactured, and the drive voltage, current efficiency and luminance half time were measured. The results are shown in Table 1.

Examples 17 to 30 (element evaluation)
Compound (F5), (B4), (C18), (D16), (E13), (G1), (H1), (J5), (K1), (N6), (P1) instead of compound (D5). ), (Q1), (R4) or (S1), but the same organic EL element as in Example 16 was produced. Table 1 shows the drive voltage and current efficiency when a current of 20 mA / cm ² is applied.

Comparative Examples 1 to 4
Same as Example 16 except that compound (D5) was changed to 4,4'-bis (carbazol-9-yl) biphenyl (CBP), compound (a), compound (b) or compound (c). An organic EL element was manufactured. Table 1 shows the drive voltage and current efficiency when a current of 20 mA / cm ² is applied.

The organic EL device containing the quinoxaline compound of the present invention having good bipolarity can be expected to improve the recombination efficiency of electrons and holes in the light emitting layer. Therefore, the quinoxaline compound of the present invention can provide an organic EL device having high luminance and efficiency and excellent life.

Claims (5)

A quinoxaline compound represented by the general formula (1).

(During the ceremony,
R ¹ and R ² each independently represent a phenyl group, a biphenyl group, or a naphthyl group .
R ³ to R ⁵ represent a hydrogen atom .
Z is a substituent represented by the following general formula (3). )

(During the ceremony,
R ⁹ and R ¹⁰ represent a hydrogen atom .
R8 is an unsubstituted aromatic hydrocarbon group having ⁷ to 20 carbon atoms .
Methyl group, ethyl group, linear, branched or cyclic alkyl group with 3 to 18 carbon atoms, phenyl group, biphenyl group, naphthyl group, phenanthryl group, pyridyl group, quinolyl group, pyrimidyl group, diphenylpyridyl group, diphenylpyryl An aromatic hydrocarbon group having 6 to 20 carbon atoms and having at least one substituent selected from the group consisting of a midyl group, a diphenyltriazyl group, a dibenzothienyl group, a dibenzofuranyl group, a cyano group, and a heavy hydrogen atom.
An unsubstituted heteroaromatic group having 3 to 20 carbon atoms, or
Methyl group, ethyl group, linear, branched or cyclic alkyl group with 3 to 18 carbon atoms, phenyl group, biphenyl group, naphthyl group, phenanthryl group, pyridyl group, quinolyl group, pyrimidyl group, diphenylpyridyl group, diphenylpyryl Represents a heteroaromatic group having 3 to 20 carbon atoms and having at least one substituent selected from the group consisting of a midyl group, a diphenyltriazyl group, a dibenzothienyl group, a dibenzofuranyl group, a cyano group, and a heavy hydrogen atom. .. ) A quinoxaline compound represented by the general formula (1).

(During the ceremony,
R ¹ and R ² are independent of each other and have a phenyl group, a biphenyl group, or a naphthyl group.
Represents.
R ³ to R ⁵ represent a hydrogen atom .
Z is a substituent represented by the following general formula (4). )

(During the ceremony,
R ¹² and R ¹³ represent a hydrogen atom .
R ¹¹ is an unsubstituted aromatic hydrocarbon group having 7 to 20 carbon atoms .
Methyl group, ethyl group, linear, branched or cyclic alkyl group with 3 to 18 carbon atoms, phenyl group, biphenyl group, naphthyl group, phenanthryl group, pyridyl group, quinolyl group, pyrimidyl group, diphenylpyridyl group, diphenylpyryl An aromatic hydrocarbon group having 6 to 20 carbon atoms and having at least one substituent selected from the group consisting of a midyl group, a diphenyltriazyl group, a dibenzothienyl group, a dibenzofuranyl group, a cyano group, and a heavy hydrogen atom.
An unsubstituted heteroaromatic group having 3 to 20 carbon atoms, or
Methyl group, ethyl group, linear, branched or cyclic alkyl group with 3 to 18 carbon atoms, phenyl group, biphenyl group, naphthyl group, phenanthryl group, pyridyl group, quinolyl group, pyrimidyl group, diphenylpyridyl group, diphenylpyryl Represents a heteroaromatic group having 3 to 20 carbon atoms and having at least one substituent selected from the group consisting of a midyl group, a diphenyltriazyl group, a dibenzothienyl group, a dibenzofuranyl group, a cyano group, and a heavy hydrogen atom. .. ) R ⁸ and R ¹¹ are independent of each other.
Unsubstituted, naphthyl group, fluorenyl group, phenanthryl group, pyridyl group, pyrimidyl group, triazil group, quinolyl group, quinazolyl group, dibenzofuranyl group or dibenzothienyl group, or independently of each of methyl group, phenyl group, Selected from the group consisting of a biphenyl group, a naphthyl group, a phenanthryl group, a pyridyl group, a quinolyl group, a pyrimidyl group, a diphenylpyridyl group, a diphenylpyrimidyl group, a diphenyltriazyl group, a dibenzothienyl group, a dibenzofuranyl group, and a cyano group. A phenyl group, a naphthyl group, a fluorenyl group, a phenanthryl group, a pyridyl group, a pyrimidyl group, a triazil group, a quinolyl group, a quinazolyl group, a dibenzofuranyl group, or a dibenzothienyl group, which have one or more substituents.
The quinoxaline compound according to claim 1 or 2, wherein the quinoxaline compound is characterized by the above. R ⁸ and R ¹¹ are independent of each other, methylphenyl group, naphthyl group, biphenyl group, terphenyl group, dimethylfluorenyl group, phenanthryl group, naphthylphenyl group, phenanthrylphenyl group, pyridyl group, diphenyl. Pyridyl group, diphenylpyrimidyl group, diphenyltriazyl group, quinolyl group, quinazolyl group, phenylquinazolyl group, biphenylquinazolyl group, dibenzofuranyl group, dibenzothienyl group, pyridylphenyl group, diphenylpyrimidylphenyl The quinoxalin compound according to any one of claims 1 to 3, which is a group, a diphenyltriazylphenyl group, a dibenzofuranylphenyl group, or a dibenzothienylphenyl group. A luminescent material containing the quinoxaline compound according to any one of claims 1 to 4.