Organic compound, light-emitting element and display panel

Abstract

To provide an organic compound, a light-emitting element, and a display panel for providing light-emitting materials with excellent performance such as luminous efficiency, stability and lifetime.SOLUTION: Embodiments of the present disclosure disclose an organic compound, a light-emitting element, and a display panel. The organic compound has a structure (1) represented by formula (1). The present invention uses the organic compound containing amino groups, and the presence of amino groups together with heterocycles in the organic compound enhances the resonance effect of the material applied to the light-emitting element, improves the performance of the material, increases the luminous efficiency of the light-emitting element and increases the luminous lifetime of the light-emitting element.SELECTED DRAWING: Figure 1

Description

[Technical Field]

[0001] The present invention relates to the field of displays, and in particular to organic compounds, light-emitting elements and display panels. [Background technology]

[0002] Currently, organic electroluminescent devices typically have a positive electrode, a negative electrode, and an organic layer between them. Organic materials in the organic layer are used to convert electrical energy into light energy, thereby achieving organic electroluminescence. To improve the luminous efficiency and service life of organic electroluminescent devices, multiple organic layers are often used, each containing a different organic material. Specifically, the organic layers mainly include a hole injection layer, a hole transport layer, an emissive layer, an electron transport layer, and an electron injection layer. By applying a voltage between the positive and negative electrodes of the organic electroluminescent device, the positive electrode injects holes into the organic layer, and the negative electrode injects electrons into the organic layer. The injected holes and electrons meet to form excitons, which then emit light upon transition to the ground state, thereby achieving the light emission of the organic electroluminescent device. Organic electroluminescent devices have the advantages of self-luminescence, high brightness, high efficiency, low-voltage operation, wide viewing angles, high contrast, and fast response, making organic electroluminescent devices expected to be widely used.

[0003] Accordingly, the development of materials for organic light-emitting diodes (OLEDs) has attracted widespread attention due to a series of advantages such as synthetic versatility, simple composition, and easy processing. In addition, in order to improve the luminous efficiency of organic electroluminescence devices, various material systems for the energy transfer and conversion mechanism have been attempted, but the luminescent materials applied to OLED devices still have poor performance in terms of luminous efficiency, stability, and lifespan, restricting the improvement of the performance of OLED devices. Summary of the Invention [Problem to be solved by the invention]

[0004] Therefore, there is an urgent need for an organic compound, a light-emitting device, and a display panel that can solve the above technical problems. [Means for solving the problem]

[0005] The present invention provides an organic compound, a light-emitting device, and a display panel that can alleviate the technical problem that the performance of OLED devices is difficult to improve due to the poor performance of luminescent materials currently used in OLED devices, such as luminous efficiency, stability, and lifespan.

[0006] The present invention relates to a compound having a structure represented by general formula (1), [ka] wherein Z is selected from CR1R2, NR3, O or S; X is selected from O or NR4; R1-R4, at each occurrence, are independently selected from a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 29 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 26 to 36 carbon atoms; R1 and R2 may be linked to each other to form a ring or may not form a ring; Ar1 is selected from H, D, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 20 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 12 to 20 carbon atoms; Ar2 and Ar3 are each independently selected from a methyl group, a substituted or unsubstituted aromatic group having 7 to 18 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 12 to 16 carbon atoms; Ar4 to Ar6 each independently provide an organic compound selected from a substituted or unsubstituted aromatic group having 6 to 31 carbon atoms and a substituted or unsubstituted heteroaromatic group having 6 to 26 carbon atoms.

[0007] Preferably, the organic compound has a structure represented by any one of general formulas (2) to (11). [ka]

[0008] Preferably, the organic compound has a structure represented by general formula (12): [ka] wherein Y is selected from CR5R6, NR7, O or S; R5 to R7, at each occurrence, are independently selected from a substituted or unsubstituted methyl group and a substituted or unsubstituted aromatic group having 6 to 10 carbon atoms; R5 and R6 are bonded to each other to form a ring or do not form a ring; Ar7 and Ar8 are each independently selected from substituted or unsubstituted aromatic groups having 6 to 10 carbon atoms; Ar9 is selected from substituted or unsubstituted phenyl groups.

[0009] Preferably, R5 to R7, at each occurrence, are each independently selected from a methyl group, a substituted or unsubstituted phenyl group; Ar7 to Ar8 are each independently selected from a methyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group; Ar9 is independently selected from a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group.

[0010] Preferably, the organic compound has a structure represented by general formula (13): [ka] In the formula, A is CR9R 10 , N.R. 11 , O or S; n represents an integer of 0 to 4, R8~R11 are each independently selected at each occurrence from a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms and a substituted or unsubstituted aromatic group having 6 to 10 carbon atoms; If n is equal to 0, R9, R 10 may or may not be linked to each other to form a ring, and when n is 1 or more, R and R and / or R 10 may or may not be linked to each other to form a ring.

[0011] Preferably, the organic compound has a structure represented by general formula (14): [ka] In the formula, Ar 10 ~Ar 11 are each independently selected from a methyl group, a substituted or unsubstituted aromatic group having 6 to 18 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 13 carbon atoms; Ar 12 is selected from substituted or unsubstituted phenyl groups.

[0012] Preferably, Ar 10 ~Ar 11 are each independently selected from a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group.

[0013] Preferably, Ar1 is selected from H, D, a methyl group, an isopropyl group, a tertiary butyl group, a tert-amyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted dibenzofuran group, a substituted or unsubstituted dibenzothiophene group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted amino group; Ar2 to Ar3 are each independently selected from a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group; Ar4 to Ar6 are each independently selected from a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group; R1 to R4 are each independently selected from a methyl group and a substituted or unsubstituted phenyl group.

[0014] Preferably, the organic compound is selected from the following compounds: [ka] [ka] [ka] [ka] [ka] [ka] [ka] [ka] [ka]

[0015] The present invention provides a pair of electrodes including a first electrode and a second electrode; an organic functional layer located between the first electrode and the second electrode; wherein the material of the organic functional layer comprises one or more of the organic compounds described in any one of the above items.

[0016] Preferably, the organic functional layer comprises at least an emitting layer, the emitting layer comprising a host material and a guest material, and the guest material is one or more of the organic compounds described in any one of the above items.

[0017] The present invention further provides a display panel comprising any one of the light-emitting devices described above.

[0018] The present invention uses an amino group-containing organic compound, which has an amino group in addition to a heterocycle, thereby enhancing the resonance effect of the material used in the light-emitting device, improving the performance of the material, and increasing the luminous efficiency and luminous life of the light-emitting device. [Brief explanation of the drawings]

[0019] In order to more clearly describe the technical solutions in the embodiments of the present invention, the following will briefly describe the drawings used in the description of the embodiments. Of course, the drawings described below are only a part of the embodiments of the present invention, and those skilled in the art can come up with other drawings based on these drawings without any creative efforts. [Figure 1] 1 is a first structural schematic diagram of a light-emitting device provided in an embodiment of the present invention; [Figure 2] FIG. 2 is a second structural schematic diagram of the light-emitting device provided in the embodiment of the present invention. DETAILED DESCRIPTION OF THE INVENTION

[0020] The technical solutions of the embodiments of the present invention will be described clearly and completely below with reference to the drawings in the embodiments of the present invention. It should be understood that the described embodiments are merely a part of the embodiments of the present invention, not all of them. Based on the embodiments of the present invention, all other embodiments obtained by those skilled in the art without any creative effort fall within the scope of protection of the present invention. It should also be understood that the specific embodiments described herein are merely for the purpose of explaining and interpreting the present invention, and are not intended to limit the present invention. In the present invention, unless otherwise specified, the directions used, such as "up" and "down," generally refer to the up and down of the device in actual use or operation, specifically to the drawing direction in the drawings, while "inside" and "outside" refer to the contour of the device. In the present invention, "optionally," "optionally," and "selectively" mean that they may or may not be present, i.e., they refer to one of two alternative solutions, "present" or "absent." When multiple "selectively" exist in a technical solution, each "selectively" is independent of the other, unless otherwise specified and without contradiction or mutual constraint. In the present invention, technical features described openly include closed technical solutions consisting of the recited features and open technical solutions including the recited features.

[0021] In the present invention, aromatic group, aromatic, and aromatic ring system have the same meaning and can be interchanged.

[0022] In the present invention, the terms heteroaromatic group, heteroaromatic and heteroaromatic ring system have the same meaning and can be interchanged.

[0023] In the present invention, the term "substituted" means that a hydrogen atom in a substituent is replaced with a substituent.

[0024] In the present invention, when the same substituent appears multiple times, they can be independently selected from different groups. For example, when a general formula includes multiple R, R can be independently selected from different groups.

[0025] In the present invention, "substituted or unsubstituted" means that the defined group may be substituted or unsubstituted. When the defined group is substituted, it should be understood that the defined group may be substituted with one or more substituents R, wherein R is selected from the group consisting of a deuterium atom, a cyano group, an isocyano group, a nitro group, a halogen atom, an alkyl group containing 1 to 20 carbon atoms, a heterocyclic group containing 3 to 20 ring atoms, an aromatic group containing 6 to 20 ring atoms, a heteroaromatic group containing 5 to 20 ring atoms, -NR'R'', a silanyl group, a carbonyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, a carbamoyl group, a haloformyl group, a formyl group, an isocyanate group, a thiocyanate group, an isothiocyanate group, a hydroxyl group, and a trifluoromethyl group, and the above groups may be further substituted with substituents acceptable in the art. It should be understood that R' and R'' in -NR'R'' are each independently selected from H, a deuterium atom, a cyano group, an isocyano group, a nitro group or a halogen, an alkyl group containing 1 to 10 carbon atoms, a heterocyclic group containing 3 to 20 ring atoms, an aromatic group containing 6 to 20 ring atoms, and a heteroaromatic group containing 5 to 20 ring atoms, but are not limited to these. Preferably, R is selected from a deuterium atom, a cyano group, an isocyano group, a nitro group, or a halogen, an alkyl group containing 1 to 10 carbon atoms, a heterocyclic group containing 3 to 10 ring atoms, an aromatic group containing 6 to 20 ring atoms, a heteroaromatic group containing 5 to 20 ring atoms, a silanyl group, a carbonyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, a carbamoyl group, a haloformyl group, a formyl group, an isocyanate group, a thiocyanate group, an isothiocyanate group, a hydroxyl group, and a trifluoromethyl group, but is not limited thereto, and the above groups may be further substituted with substituents accepted in the art.

[0026] In the present invention, the "number of ring atoms" refers to the number of atoms constituting the ring itself of a structural compound in which atoms are bonded to form a ring (e.g., a monocyclic compound, a fused ring compound, a bridged compound, a carbocyclic compound, or a heterocyclic compound). When the ring is substituted with a substituent, the atoms contained in the substituent are not included in the ring-forming atoms. The same applies to the "number of ring atoms" described below unless otherwise specified. For example, a benzene ring has 6 ring atoms, a naphthalene ring has 10 ring atoms, and a thienyl group has 5 ring atoms.

[0027] In the present invention, an "aryl group or aromatic group" refers to an aromatic hydrocarbon group derived by removing one hydrogen atom from an aromatic ring compound. It may be a monocyclic aryl group, a fused-ring aryl group, or a polycyclic aryl group, and in the case of a polycyclic ring, at least one of the rings is an aromatic ring system. For example, a "substituted or unsubstituted aryl group having 6 to 40 ring atoms" refers to an aryl group having 6 to 40 ring atoms, preferably a substituted or unsubstituted aryl group having 6 to 30 ring atoms, more preferably a substituted or unsubstituted aryl group having 6 to 18 ring atoms, and particularly preferably a substituted or unsubstituted aryl group having 6 to 14 ring atoms, and the aryl group may be optionally further substituted. Suitable examples include, but are not limited to, phenyl, biphenyl, terphenyl, naphthyl, anthryl, phenanthryl, tetrahydrofluoranthene, triphenylene, pyrenyl, perylenyl, naphthacene, fluorenyl, perylene, acenaphthyl, and derivatives thereof. It is understood that multiple aryl groups may be interrupted by short non-aromatic units (e.g., atoms other than H, such as C, N, or O atoms, e.g., <10%), and specifically, for example, acenaphthylene, fluorene, or 9,9-diarylfluorene, triarylamine, and diaryl ether systems are also included in the definition of an aryl group.

[0028] In the present invention, the term "heteroaryl group or heteroaromatic group" refers to an aryl group in which at least one carbon atom is replaced with a non-carbon atom, and the non-carbon atom may be an N atom, an O atom, an S atom, etc. For example, the term "substituted or unsubstituted heteroaryl group having 5 to 40 ring atoms" refers to a heteroaryl group having 5 to 40 ring atoms, preferably a substituted or unsubstituted heteroaryl group having 6 to 30 ring atoms, more preferably a substituted or unsubstituted heteroaryl group having 6 to 18 ring atoms, and particularly preferably a substituted or unsubstituted heteroaryl group having 6 to 14 ring atoms, and the heteroaryl group is optionally further substituted. Suitable examples include thienyl, furyl, pyrrolyl, imidazolyl, diazolyl, triazolyl, imidazolyl, pyridyl, bipyridyl, pyrimidyl, triazyl, acridinyl, pyridazyl, pyrazinyl, quinolyl, isoquinolyl, quinazolyl, quinoxaline, phthalazine, pyridopyrimidyl, pyridopyrazinyl, benzothienyl, benzofuryl, and indolyl. Groups include, but are not limited to, pyrroloimidazolyl group, pyrrolopyrrolyl group, thienopyrrolyl group, thienothienyl group, furopyrrolyl group, furofuryl group, thienofuryl group, benzisoxazole group, benzisothiazole group, benzimidazolyl group, O-diazonaphthyl group, phenanthridine group, perimidine group, quinazolone group, dibenzothiophene group, dibenzofuran group, carbazolyl group and derivatives thereof.

[0029] In the present invention, an "amino group" is a derivative of an amine having the structural characteristics of the formula --NR'R'' where R' and R'' have the same meanings as above.

[0030] In the present invention, the "*" attached to a single bond represents a bonding site or a condensation site, and when no bonding site is specified in a group, any bonding site in the group is used as a bonding site. When the same group contains multiple substituents with the same symbol, each substituent may be the same or different, for example, [ka] The six R on the benzene ring may be the same or different. The fact that the single bond to which a substituent is bonded passes through the corresponding ring means that the substituent can be bonded to any position on the ring, for example: [ka] The R in the formula binds to any substitutable site on the benzene ring.

[0031] Currently, the luminescent materials used in OLED devices have poor performance in terms of luminous efficiency, stability, and lifespan, making it difficult to improve the performance of OLED devices.

[0032] An embodiment of the present invention provides an organic compound, the organic compound having a structure represented by general formula (1): [ka] wherein Z is selected from CR1R2, NR3, O or S; X is selected from O or NR4; R1-R4, at each occurrence, are independently selected from a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 36 carbon atoms; R1 and R2 may be linked to each other to form a ring or may not form a ring; Ar1 is selected from H, D, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 30 carbon atoms; Ar2 and Ar3 are each independently selected from a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 30 carbon atoms; Ar4 to Ar6 are each independently selected from substituted or unsubstituted aromatic groups having 6 to 31 carbon atoms and substituted or unsubstituted heteroaromatic groups having 5 to 30 carbon atoms.

[0033] The present invention uses an amino group-containing organic compound, which has an amino group in addition to a heterocycle, thereby enhancing the resonance effect of the material used in the light-emitting device, improving the performance of the material, and increasing the luminous efficiency and luminous life of the light-emitting device.

[0034] In some embodiments, the organic compound has a structure represented by any one of general formulas (2) to (11). [ka]

[0035] In some embodiments, Z is preferably selected from CR1R2, O, or S, and more preferably O or S.

[0036] In some embodiments, X is preferably NR4.

[0037] In some embodiments, the organic compound has a structure represented by general formula (12): [ka]

[0038] In some embodiments, Y is selected from CR5R6, NR7, O, or S.

[0039] In some embodiments, R5 to R7, at each occurrence, are each independently selected from a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 30 carbon atoms. R5 to R7, at each occurrence, are each independently, preferably, selected from a substituted or unsubstituted alkyl group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 20 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 20 carbon atoms. R5 to R7, at each occurrence, are each independently, preferably, selected from a substituted or unsubstituted alkyl group having 1 to 8 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 15 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 15 carbon atoms. R5 to R7, at each occurrence, are each independently, preferably, selected from a substituted or unsubstituted methyl group and a substituted or unsubstituted aromatic group having 6 to 10 carbon atoms. R5 to R7 at each occurrence are each independently selected from a methyl group and a substituted or unsubstituted phenyl group.

[0040] In some embodiments, R5 and R6 may or may not be linked to each other to form a ring.

[0041] In some embodiments, Ar7 to Ar8 are each independently selected from a substituted or unsubstituted alkyl group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 20 carbon atoms, or a substituted or unsubstituted heteroaromatic group having 5 to 20 carbon atoms. Ar7 to Ar8 are each independently preferably selected from a substituted or unsubstituted alkyl group having 1 to 8 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 15 carbon atoms, or a substituted or unsubstituted heteroaromatic group having 5 to 15 carbon atoms. Ar7 to Ar8 are each independently more preferably selected from a substituted or unsubstituted aromatic group having 6 to 10 carbon atoms, or a substituted or unsubstituted heteroaromatic group having 5 to 10 carbon atoms. Ar7 to Ar8 are each independently selected from a methyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group.

[0042] In some embodiments, Ar9 is independently selected from a substituted or unsubstituted aromatic group having 6 to 20 carbon atoms and a substituted or unsubstituted heteroaromatic group having 5 to 20 carbon atoms. Ar9 is independently selected from a substituted or unsubstituted aromatic group having 6 to 15 carbon atoms and a substituted or unsubstituted heteroaromatic group having 5 to 15 carbon atoms. Ar9 is independently selected from a substituted or unsubstituted aromatic group having 6 to 10 carbon atoms and a substituted or unsubstituted heteroaromatic group having 5 to 10 carbon atoms. Ar9 is independently selected from a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran group, a substituted or unsubstituted dibenzothiophene group, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group.

[0043] In some embodiments, the organic compound has a structure represented by general formula (13): [ka]

[0044] In some embodiments, A is CR9R 10 , N.R. 11 , O or S; In some embodiments, n represents an integer from 0 to 4, for example, 0, 1, 2, 3, or 4.

[0045] In some embodiments, R to R 11 R8 to R9, when each appearing, are independently selected from a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 30 carbon atoms. 11 R8 to R9 are each independently selected from a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 30 carbon atoms. 11R8 to R9 are each independently selected from substituted or unsubstituted alkyl groups having 1 to 4 carbon atoms and substituted or unsubstituted aromatic groups having 6 to 10 carbon atoms. 11 is, at each occurrence, preferably selected independently from a methyl group, a tertiary butyl group, and a substituted or unsubstituted phenyl group, where the substituted phenyl group is preferably a tertiary butyl-substituted phenyl group.

[0046] If n is equal to 0, R9, R 10 When n is 1 or more, R and R and / or R 10 are linked together to form a ring or not to form a ring. That is, when n is 1 or more, R, R, R 10 The three may form a ring in pairs, may form a ring together, or may not form a ring at all.

[0047] In some embodiments, the organic compound has a structure represented by general formula (14): [ka]

[0048] In some embodiments, Ar 10 ~Ar 11 are each independently preferably selected from a substituted or unsubstituted alkyl group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 24 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 24 carbon atoms. 10 ~Ar 11 are each independently preferably selected from a substituted or unsubstituted alkyl group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 20 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 20 carbon atoms. 10 ~Ar 11 are each independently preferably selected from a substituted or unsubstituted alkyl group having 1 to 8 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 15 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 15 carbon atoms. 10 ~Ar11 are each independently selected from a methyl group, a substituted or unsubstituted aromatic group having 6 to 18 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 13 carbon atoms. 10 ~Ar 11 are each independently selected from a methyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group.

[0049] In some embodiments, Ar 12 is selected from substituted or unsubstituted phenyl groups.

[0050] In the above examples, R1 to R4, when appearing in each occurrence, are each independently selected from a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 30 carbon atoms. R1 to R4, when appearing in each occurrence, are each independently selected from a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 29 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 26 to 36 carbon atoms. R1 to R4, when appearing in each occurrence, are each independently selected from a substituted or unsubstituted alkyl group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 15 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 15 carbon atoms. R4, when it occurs, is more preferably selected from methyl, substituted or unsubstituted phenyl, substituted or unsubstituted naphthyl, substituted or unsubstituted dibenzofuran, substituted or unsubstituted dibenzothiophene, substituted or unsubstituted fluorenyl, and substituted or unsubstituted carbazolyl. R1 to R4, when it occurs, are each more preferably selected from methyl and substituted or unsubstituted phenyl.

[0051] In the above examples, Ar1 is preferably selected from H, D, a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 30 carbon atoms. Ar1 is preferably selected from H, D, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 20 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 12 to 20 carbon atoms. Ar1 is preferably selected from H, D, a substituted or unsubstituted alkyl group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 20 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 20 carbon atoms. Ar1 is more preferably selected from H, D, a substituted or unsubstituted alkyl group having 1 to 8 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 15 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 15 carbon atoms. Ar1 is more preferably selected from H, D, a methyl group, an isopropyl group, a tertiary butyl group, a tert-amyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted carbazolyl group, and a substituted or unsubstituted amino group.

[0052] In the above examples, Ar2 to Ar3 are each independently preferably selected from a substituted or unsubstituted methyl group, a substituted or unsubstituted aromatic group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 30 carbon atoms. Ar2 to Ar3 are each independently preferably selected from a methyl group, a substituted or unsubstituted aromatic group having 7 to 18 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 12 to 16 carbon atoms. Ar2 to Ar3 are each independently preferably selected from a substituted or unsubstituted alkyl group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 20 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 20 carbon atoms. Ar2 to Ar3 are each independently preferably selected from a substituted or unsubstituted alkyl group having 1 to 8 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 15 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 15 carbon atoms. Ar2 to Ar3 are each more preferably independently selected from a methyl group, a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group.

[0053] In the above examples, Ar4 to Ar6 are each independently preferably selected from a substituted or unsubstituted aromatic group having 6 to 31 carbon atoms and a substituted or unsubstituted heteroaromatic group having 6 to 26 carbon atoms. Ar4 to Ar6 are each independently preferably selected from a substituted or unsubstituted aromatic group having 6 to 20 carbon atoms and a substituted or unsubstituted heteroaromatic group having 5 to 20 carbon atoms. Ar4 to Ar6 are each independently preferably selected from a substituted or unsubstituted aromatic group having 6 to 15 carbon atoms and a substituted or unsubstituted heteroaromatic group having 5 to 15 carbon atoms. Ar4 to Ar6 are each independently more preferably selected from a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran group, a substituted or unsubstituted dibenzothiophene group, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group.

[0054] In some embodiments, the organic compound is selected from the following compounds: [ka] [ka] [ka] [ka] [ka] [ka] [ka] [ka] [ka]

[0055] The amino group-containing organic compound provided in the embodiments of the present invention has an amino group together with a heterocycle, which enhances the resonance effect of the material applied to the light-emitting device, improves the performance of the material, and increases the luminous efficiency and luminous life of the light-emitting device.

[0056] 1 and 2, the present invention further provides a light-emitting device, which includes a pair of electrodes including a first electrode 101 and a second electrode 102, and an organic functional layer 103 located between the first electrode 101 and the second electrode 102, where the material of the organic functional layer 103 includes one or more of the organic compounds described above. The first electrode 101 may be an anode, and the second electrode 102 may be a cathode.

[0057] In some embodiments, the light-emitting device can be applied to organic light-emitting diodes, organic photovoltaic cells, organic light-emitting cells, organic field-effect transistors, organic light-emitting field-effect transistors, organic lasers, organic spintronic devices, organic sensors, organic plasmonic light-emitting diodes, etc., and is preferably an organic light-emitting diode, an organic light-emitting cell, or an organic light-emitting field-effect transistor.

[0058] In some embodiments, the light emitting device can be applied to various electronic devices, such as display panels, lighting devices, and light sources.

[0059] In some embodiments, the organic functional layer 103 may be a single layer, in which case the organic functional layer 103 is a mixture layer, the mixture layer including a first compound and a second compound, the first compound being one or more selected from the organic compounds described above, and the second compound being one or more selected from a hole injection material, a hole transport material, an electron transport material, a hole blocking material, an emitting guest material, an emitting host material, and an organic dye.

[0060] When the second compound is one or more selected from a hole injection material, a hole transport material, an electron transport material, a hole blocking material, a light-emitting host material, and an organic dye, the mass ratio of the first compound to the second compound is 1:99 to 30:70, and preferably 1:99 to 10:90.

[0061] When the second compound is a light-emitting guest material, the mass ratio of the first compound to the second compound is 99:1 to 70:30, and preferably 99:1 to 90:10.

[0062] In some embodiments, the organic functional layer 103 may include multiple layers. When the organic functional layer 103 is a multilayer, the organic functional layer 103 includes at least an emitting layer 107. Preferably, the organic functional layer 103 includes a hole injection layer 104, a hole transport layer 105, an emitting layer 107, an electron blocking layer 106, an electron injection layer 109, an electron transport layer 108, or a hole blocking layer.

[0063] In some embodiments, the light-emitting element may be a blue light-emitting element, a green light-emitting element, or a red light-emitting element. The light-emitting layer 107 may include a host material and a guest material, where the guest material is one or more of the organic compounds described above, and the host material includes a fused aromatic derivative or a heteroaromatic compound.

[0064] The light emitting element has an emission wavelength of 300 to 1000 nm, and further has an emission wavelength of 350 to 900 nm, and further has an emission wavelength of 400 to 800 nm.

[0065] In some embodiments, the host material comprises at least one of anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, tetrahydrofluoranthene compounds, carbazole derivatives, dibenzofuran derivatives, ladder-type furan compounds, and pyrimidine derivatives.

[0066] In some embodiments, the mass ratio of the host material to the guest material is 99:1 to 70:30, such as 90:10, 85:15, 80:20, 75:25, etc. Preferably, it is 99:1 to 90:10, such as 97:3, 96:4, 95:5, 93:7, 92:8, etc. When the guest material is dispersed in the host material and the mass ratio of the host material to the guest material is 99:1 to 70:30, this contributes to suppressing crystallization of the light-emitting layer 107 and also suppresses concentration quenching of the guest material due to high concentration, thereby improving the luminous efficiency of the light-emitting device.

[0067] In some embodiments, the anode is a hole-injecting electrode, and can inject holes into the organic functional layer 103, for example, the anode injects holes into the hole injection layer, the hole transport layer, or the light-emitting layer. The anode may include at least one of a conductive metal, a conductive metal oxide, or a conductive polymer. Preferably, the absolute value of the difference between the work function of the anode and the HOMO (Highest Occupied Molecular Orbital) energy level or the valence band energy level of the light-emitting material in the light-emitting layer or the p-type semiconductor material in the hole injection layer, hole transport layer, or electron blocking layer is less than 0.5 eV, preferably less than 0.3 eV, and more preferably less than 0.2 eV. The anode material may include, but is not limited to, at least one of Al, Cu, Au, Ag, Mg, Fe, Co, Ni, Mn, Pd, Pt, ITO (indium tin oxide), aluminum-doped zinc oxide (AZO), etc., or other suitable known anode materials, which can be readily selected and used by those skilled in the art. The anode material may be deposited using any suitable technique, such as a suitable physical vapor deposition method, including, for example, radio frequency magnetron sputtering, vacuum thermal evaporation, electron beam (e-beam), etc. In some embodiments, the anode may be patterned; for example, patterned ITO conductive substrates are commercially available and can be used to fabricate the light-emitting device of the present invention.

[0068] In some embodiments, the cathode is an electrode that injects electrons, and can inject electrons into the organic functional layer, for example, the cathode injects electrons into the electron injection layer, the electron transport layer, or the light-emitting layer. The cathode may include at least one of a conductive metal or a conductive metal oxide. Preferably, the absolute value of the difference between the work function of the cathode and the LUMO (Lowest Unoccupied Molecular Orbital) energy level or the conduction band energy level of the light-emitting material in the light-emitting layer, or the n-type semiconductor material as the electron injection layer, the electron transport layer, or the hole-blocking layer is less than 0.5 eV, preferably less than 0.3 eV, and more preferably less than 0.2 eV. Any material that can be used as a cathode in an organic electronic device can be used as a cathode material in the device of the present application, including, but not limited to, at least one of Al, Au, Ag, Ca, Ba, Mg, LiF / Al, MgAg alloy, BaF2 / Al, Cu, Fe, Co, Ni, Mn, Pd, Pt, ITO, etc. The cathode material can be deposited using any suitable technique, such as a suitable physical vapor deposition method, including, for example, radio frequency magnetron sputtering, vacuum thermal evaporation, electron beam (e-beam), etc.

[0069] In some embodiments, the hole injection layer 104 is used to facilitate the injection of holes from the anode to the light-emitting layer 107. The hole injection layer 104 includes a hole injection material that can accept holes injected from the anode at a low voltage. Preferably, the highest occupied molecular orbital (HOMO) of the hole injection material is between the work function of the anode material and the HOMO of the functional material into which the holes are injected in the film layer away from the anode (e.g., the hole transport material of the hole transport layer). The hole injection material can include, but is not limited to, at least one of metal porphyrins, oligothiophenes, arylamine-based organic materials, hexanitrile hexaazabenzophenanthrene-based organic materials, quinacridone-based organic materials, perylene-based organic materials, anthraquinones, polyanilines, and polythiophene-based conductive polymers.

[0070] In some embodiments, the hole transport layer 105 can be used to transport holes to the light-emitting layer 107, and the hole transport layer 105 includes a hole transport material that receives holes transported from the anode or the hole injection layer and transfers the holes to the light-emitting layer. The hole transport material is a material known in the art that has high hole mobility, and the hole transport material may include, but is not limited to, at least one of an arylamine-based organic material, a conductive polymer, a block copolymer having both conjugated and non-conjugated portions, etc.

[0071] In some embodiments, the electron transport layer 108 is used to transport electrons, and the electron transport layer 108 includes an electron transport material that receives electrons injected from a negative electrode and transfers the electrons to the light-emitting layer 107. The electron transport material is a material known in the art that has high electron mobility, and may include, but is not limited to, at least one of an 8-quinolinol Al complex, an Alq3-containing complex, an organic radical compound, a hydroxyflavone-metal complex, 8-quinolinol lithium (LiQ), and a benzimidazole-based compound.

[0072] In some embodiments, the electron injection layer 109 is used to inject electrons, and the electron injection layer 109 includes an electron injection material. The electron injection material preferably has the ability to transport electrons, is effective in injecting electrons from the negative electrode, is excellent in injecting electrons into the light-emitting layer 107 or the light-emitting material, prevents excitons generated in the light-emitting layer 107 from migrating to the hole injection layer, and has excellent thin-film formability. The electron injection material includes, but is not limited to, at least one of 8-quinolinol lithium (LiQ), fluorenone, anthraquinodimethane, diphenylquinone, thiopyran dioxide, azole, diazole, triazole, imidazole, perylene tetracarboxylic acid, fluorenylidenemethane, anthrone, etc., and derivatives thereof, metal complex compounds, nitrogen-containing five-membered ring derivatives, etc.

[0073] In some embodiments, the hole blocking layer is used to block holes from reaching the negative electrode and may generally be formed under the same conditions as the hole injection layer 104. The hole blocking layer includes a hole blocking material, which may include, but is not limited to, at least one of a diazole derivative or a triazole derivative, a phenanthroline derivative, BCP, an aluminum complex, and the like.

[0074] Referring to FIG. 1 , in some embodiments, the light-emitting device further includes a substrate 110, in which the first electrode 101, the hole injection layer 104, the hole transport layer 105, the electron blocking layer 106, the light-emitting layer 107, the electron transport layer 108, the electron injection layer 109, and the second electrode 102 are sequentially stacked on the substrate 110. Referring to FIG. 2 , the first electrode 101, the hole injection layer 104, the hole transport layer 105, the light-emitting layer 107, the electron transport layer 108, the electron injection layer 109, and the second electrode 102 are sequentially stacked on the substrate 110. The substrate 110 may be a transparent substrate or an opaque substrate. When the substrate 110 is a transparent substrate, a transparent light-emitting device can be fabricated. The substrate 110 may be a rigid substrate or an elastic flexible substrate. The material of the substrate 110 may include, but is not limited to, plastic, polymer, metal, semiconductor wafer, glass, etc. Preferably, the substrate 110 includes at least one smooth surface for forming the anode. More preferably, the surface is free of surface defects. Preferably, the material of the substrate 110 is a polymer thin film or plastic, including, but not limited to, polyethylene terephthalate (PET material) and polyethylene glycol (2,6-naphthalene) (PEN material). The vitrification temperature of the substrate 110 is 150°C or higher, preferably 200°C or higher, more preferably 250°C or higher, and most preferably 300°C or higher.

[0075] In some embodiments, the light-emitting device may be a solution-based light-emitting device, ie, at least one of the organic functional layers is prepared by printing (eg, inkjet printing).

[0076] In some embodiments, the mixture layer or the light-emitting layer can be formed by a printing or coating process of a composition. The printing or coating process includes inkjet printing, nozzle printing, letterpress printing, screen printing, dip coating, spin coating, doctor blade coating, roll printing, twist roller printing, offset printing, flexographic printing, rotary printing, spray coating, brush or pad printing, slot die coating, etc. Preferred are gravure printing, nozzle printing, and inkjet printing.

[0077] The composition may be a solution or a suspension, and may include a dispersoid and a dispersing agent, wherein the dispersoid is one or more of the organic compounds described above, and the dispersing agent is used to disperse the dispersoid.

[0078] In the composition, the mass fraction of the organic compound described above may be 0.01% to 10%, preferably 0.1% to 15%, more preferably 0.2% to 5%, and most preferably 0.25% to 3%.

[0079] Preferably, the Hansen solubility parameter of the dispersant is within the following range: δd (dispersion force) of the dispersant is 17.0 to 23.2 MPa 1 / 2 The range is preferably 18.5 to 21.0 MPa. 1 / 2 The range of δp (polarity) is 0.2 to 12.5 MPa. 1 / 2 The range is preferably 2.0 to 6.0 MPa. 1 / 2 The δh (hydrogen bonding strength) is in the range of 0.9 to 14.2 MPa. 1 / 2 The range is preferably 2.0 to 6.0 MPa. 1 / 2 The range is.

[0080] Preferably, the boiling point of the dispersant is 150° C. or higher, preferably 180° C. or higher, more preferably 200° C. or higher, more preferably 250° C. or higher, even more preferably 275° C. or higher, and most preferably ≧300° C. If the boiling point of the dispersant is at least 150° C. or higher, this is advantageous for preventing clogging of the nozzles of the inkjet printhead during inkjet printing, and the higher the boiling point, the more advantageous it is for preventing clogging.

[0081] The dispersant may include at least one organic solvent, which can be evaporated from the solvent system to form a thin film containing the functional material. The organic solvent may include at least one first organic solvent, which can be selected from aromatic or heteroaromatic solvents. Specifically, the first organic solvent may be p-diisopropylbenzene, pentylbenzene, tetralin, cyclohexylbenzene, chloronaphthalene, 1,4-dimethylnaphthalene, 3-isopropylbiphenyl, p-methylisopropylbenzene, dipentylbenzene, tripentylbenzene, pentyltoluene, o-diethylbenzene, m-diethylbenzene, p-diethylbenzene, 1,2,3,4-tetramethylbenzene, 1,2,3,5-tetramethylbenzene, 1,2,4,5-tetramethylbenzene, butylbenzene, dodecylbenzene, dihexylbenzene, dibutylbenzene, p-diisopropylbenzene, cyclohexylbenzene, dibutylbenzene, dimethylbenzene, dimethylbenzene, diisopropyl ... The alkyl methyl ether can be selected from methyl methyl ether, 3-isopropylbiphenyl, p-methylisopropylbenzene, 1-methylnaphthalene, 1,2,4-trichlorobenzene, 4,4-difluorodiphenylmethane, 1,2-dimethoxy-4-(1-propenyl)benzene, diphenylmethane, 2-phenylpyridine, 3-phenylpyridine, N-methyldiphenylamine, 4-isopropylbiphenyl, α,α-dichlorodiphenylmethane, 4-(3-phenylpropyl)pyridine, benzyl benzoate, 1,1-bis(3,4-dimethylphenyl)ethane, 2-isopropylnaphthalene, quinoline, isoquinoline, methyl 2-furancarboxylate, ethyl 2-furancarboxylate, and the like.

[0082] The first organic solvent may be selected from aromatic ketone solvents, specifically, 1-tetralone, 2-tetralone, 2-(phenylepoxy)tetralone, 6-(methoxy)tetralone, acetophenone, propiophenone, benzophenone, and derivatives thereof, such as 4-methylacetophenone, 3-methylacetophenone, 2-methylacetophenone, 4-methylpropiophenone, 3-methylpropiophenone, and 2-methylpropiophenone.

[0083] The first organic solvent may be selected from aromatic ether solvents, such as 3-phenoxytoluene, butoxybenzene, p-anisaldehyde dimethyl acetal, tetrahydro-2-phenoxy-2H-pyran, 1,2-dimethoxy-4-(1-propenyl)benzene, 1,4-benzodioxane, 1,3-dipropylbenzene, 2,5-dimethoxytoluene, 4-ethylphenylethyl ether, 1,3-dipropoxybenzene, 1,2,4-trimethoxybenzene, 4-(1-propenyl)-1,2-dimethoxybenzene, 1,3-dimethoxybenzene, glycidyl phenyl ether, dibenzyl ether, 4-tert-butylanisole, trans-p-propenylanisole, 1,2-dimethoxybenzene, 1-methoxynaphthalene, diphenyl ether, 2-phenoxymethyl ether, 2-phenoxytetrahydrofuran, and ethyl-2-naphthyl ether.

[0084] The first organic solvent may be selected from aliphatic ketones, specifically, aliphatic ketones such as 2-nonanone, 3-nonanone, 5-nonanone, 2-decanone, 2,5-hexanedione, 2,6,8-trimethyl-4-nonanone, fenchone, phorone, isophorone, and di-n-pentyl ketone, or aliphatic ethers such as amyl ether, hexyl ether, dioctyl ether, ethylene glycol dibutyl ether, diethylene glycol diethyl ether, diethylene glycol butyl methyl ether, diethylene glycol dibutyl ether, triethylene glycol dimethyl ether, triethylene glycol ethyl methyl ether, triethylene glycol butyl methyl ether, tripropylene glycol dimethyl ether, and tetraethylene glycol dimethyl ether.

[0085] The first organic solvent may be selected from organic ester solvents. Specifically, the first solvent may be selected from alkyl octanoate, alkyl sebacate, alkyl stearate, alkyl benzoate, alkyl phenylacetate, alkyl cinnamate, alkyl oxalate, alkyl maleate, alkyl lactone, alkyl oleate, etc. Particularly preferred are octyl octanoate, diethyl sebacate, diallyl phthalate, isononyl isononanoate, etc.

[0086] The organic solvent may further include a second organic solvent, which may be one or more selected from the group consisting of methanol, ethanol, 2-methoxyethanol, dichloromethane, chloroform, chlorobenzene, o-dichlorobenzene, tetrahydrofuran, anisole, morpholine, toluene, o-xylene, m-xylene, p-xylene, 1,4-dioxane, acetone, methyl ethyl ketone, 1,2-dichloroethane, 3-phenoxytoluene, 1,1,1-trichloroethane, 1,1,2,2-tetrachloroethane, ethyl acetate, butyl acetate, dimethylformamide, dimethylacetamide, dimethyl sulfoxide, tetralin, decalin, and indene.

[0087] In addition to the dispersoid and the dispersant, the composition may further contain one or more components such as a surface active compound, a lubricant, a wetting agent, a dispersant, a hydrophobizing agent, an adhesive, etc., in order to adjust viscosity and film-forming properties, improve adhesion, etc.

[0088] Exemplary methods for preparing the organic compounds provided by the present invention are shown in the following illustrative Examples 1 to 16.

[0089] Example 1 Organic compound M1( [ka] ) synthesis The synthetic route of organic compound M1 is as follows. [ka]

[0090] The specific synthesis procedure for the organic compound M1 is as follows.

[0091] Synthesis of intermediate M1-3 Under a nitrogen atmosphere, intermediate M1-1 (30.8 g, 100 mmol), M1-2 (28.1 g, 100 mmol), Pd2(dba)3 (2.76 g, 3 mmol), tri-tert-butylphosphine (1.2 g, 6 mmol), sodium tert-butoxide (18.2 g, 200 mmol), and 250 mL of anhydrous toluene were added to a 500 mL two-neck flask and heated to 60 °C with stirring for 6 h. After cooling to room temperature, the reaction mixture was quenched with water. The majority of the solvent was removed by rotary evaporation, dissolved in dichloromethane, and washed three times with water. The organic solution was collected, mixed with silica gel, and purified by column chromatography in 74% yield.

[0092] Synthesis of intermediate M1-6 Under a nitrogen atmosphere, intermediate M1-4 (19.6 g, 60 mmol), M1-5 (17.9 g, 120 mmol), Pd2(dba)3 (3.32 g, 3.6 mmol), tri-tert-butylphosphine (1.44 g, 7.2 mmol), sodium tert-butoxide (11 g, 120 mmol), and 150 mL of anhydrous toluene were added to a 500 mL two-neck flask and heated to 70 °C with stirring for 6 h. After cooling to room temperature, the reaction mixture was quenched with water and rotary evaporated to remove most of the solvent. The mixture was dissolved in dichloromethane and washed three times with water. The organic solution was collected, mixed with silica gel, and purified by column chromatography in 62% yield.

[0093] Synthesis of intermediate M1-8 Following the synthesis method of compound M1-3, compounds M1-1 and M1-2 were replaced with compounds M1-7 and M1-6, respectively, with a yield of 56%.

[0094] Synthesis of intermediate M1-9 Under a nitrogen atmosphere, intermediate M1-8 (11.9 g, 20 mmol), M1-3 (10.2 g, 20 mmol), Pd2(dba)3 (0.92 g, 1 mmol), tri-tert-butylphosphine (0.4 g, 2 mmol), sodium tert-butoxide (3.64 g, 40 mmol), and 150 mL of anhydrous toluene were added to a 500 mL two-neck flask and heated to 90 °C with stirring for 6 h. After cooling to room temperature, the reaction mixture was quenched with water and rotary evaporated to remove most of the solvent. The mixture was dissolved in dichloromethane and washed three times with water. The organic layer was collected, mixed with silica gel, and purified by column chromatography in a 65% yield.

[0095] Synthesis of organic compound M1 Under a nitrogen atmosphere, compound M1-9 (10.7 g, 10 mmol) and 80 mL of anhydrous tetrahydrofuran were added to a 250 mL three-neck flask and cooled to -30 °C. 15 mmol of tert-butyllithium solution was slowly added dropwise. After the addition, the reaction mixture was heated to 60 °C and stirred for 2 hours. The mixture was then cooled to -30 °C, 20 mmol of boron tribromide was added in one portion, and the mixture was allowed to warm to room temperature and react for 1 hour. 30 mmol of N,N-diisopropylethylamine was added, and the mixture was then slowly heated to 100 °C and reacted for 3 hours. The mixture was then cooled to room temperature and quenched with aqueous sodium acetate. Most of the solvent was removed by rotary evaporation, dissolved in dichloromethane, and washed three times with water. The organic solution was collected and rotary evaporated, followed by column chromatography purification. The yield was 28%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result for organic compound M1 was MS(ASAP)=1041.

[0096] Example 2 Organic compound M2( [ka] ) synthesis The synthetic route of organic compound M2 is as follows. [ka]

[0097] The specific synthesis procedure for the organic compound M2 is as follows.

[0098] Synthesis of intermediate M2-3 Following the synthesis method of compound M1-3, compounds M1-1 and M1-2 were replaced with compounds M2-1 and M2-2, respectively, with a yield of 76%.

[0099] Synthesis of intermediate M2-4 Under a nitrogen atmosphere, intermediate M1-6 (27.8 g, 60 mmol), compound M2-3 (50.9 g, 120 mmol), compound Pd2(dba)3 (3.32 g, 3.6 mmol), compound tri-tert-butylphosphine (1.44 g, 7.2 mmol), compound sodium tert-butoxide (11 g, 120 mmol), and 150 mL of anhydrous toluene were added to a 500 mL two-neck flask, heated to 90 °C, and stirred for 6 h. The reaction was then cooled to room temperature and quenched by adding water. The reaction mixture was rotary evaporated to remove most of the solvent, dissolved in dichloromethane, and washed three times with water. The organic solution was collected, mixed with silica gel, and purified by column chromatography in a 68% yield.

[0100] Synthesis of compound M2 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M2-4, and the yield was 25%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M2 was MS(ASAP)=1212.

[0101] Example 3 Organic compound M3( [ka] ) synthesis The synthetic route of organic compound M3 is as follows. [ka]

[0102] The specific synthesis procedure for the organic compound M3 is as follows.

[0103] Synthesis of intermediate M3-3 Under a nitrogen atmosphere, compound M3-1 (28.1 g, 100 mmol), NaOH (6 g, 150 mmol), and 150 mL of dimethylformamide were added to a 500 mL two-neck flask and allowed to react with stirring for 1 hour. Methyl iodide (15.6 g, 110 mmol) was added all at once and allowed to react with stirring for 4 hours. After the reaction was completed, the reaction solution was added to 300 mL of pure water, stirred, and then suction filtered to obtain a solid. The solid was purified by recrystallization using ethanol, dichloromethane, and a mixed solution in an 82% yield.

[0104] Synthesis of intermediate M3-4 Following the synthesis method of compound M1-3, compounds M1-1 and M1-2 were replaced with compounds M3-3 and M2-2, respectively, with a yield of 72%.

[0105] Synthesis of intermediate M3-6 Following the synthesis method of compound M1-8, compound M1-7 was replaced with compound M3-5, with a yield of 58%.

[0106] Synthesis of intermediate M3-7 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M3-4 and M3-6, respectively, with a yield of 67%.

[0107] Synthesis of compound M3 Following the synthesis method of compound M1, compound M1-9 was replaced with compound M3-7, with a yield of 27%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M3 was MS(ASAP)=1083.

[0108] Example 4 Organic compound M4( [ka] ) synthesis The synthetic route of organic compound M4 is as follows. [ka]

[0109] The specific synthesis procedure for the organic compound M4 is as follows.

[0110] Synthesis of intermediate M4-2 Following the synthesis method of compound M1-3, compounds M1-1 and M1-2 were replaced with compounds M4-1 and M2-2, respectively, with a yield of 73%.

[0111] Synthesis of intermediate M4-4 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M4-2 and M4-3, respectively, with a yield of 66%.

[0112] Synthesis of compound M4 Following the synthesis method of compound M1, compound M1-9 was replaced with compound M4-4, with a yield of 24%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M4 was MS(ASAP)=957.

[0113] Example 5 Organic compound M5( [ka] ) synthesis The synthetic route of organic compound M5 is as follows. [ka]

[0114] The specific synthesis procedure for the organic compound M5 is as follows.

[0115] Synthesis of intermediate M5-2 Following the synthesis method of compound M1-3, compound M1-1 was replaced with compound M5-1, and the yield was 75%.

[0116] Synthesis of intermediate M5-3 Following the synthesis method of compound M1-9, compound 1-3 was replaced with compound M5-2, with a yield of 68%.

[0117] Synthesis of compound M5 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M5-3, and the yield was 29%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M5 was MS(ASAP)=1015.

[0118] Example 6 Organic compound M6( [ka] ) synthesis The synthetic route of organic compound M6 is as follows. [ka]

[0119] The specific synthesis procedure for the organic compound M6 is as follows.

[0120] Synthesis of intermediate M6-1 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M5-2 and M4-3, respectively, with a yield of 64%.

[0121] Synthesis of compound M6 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M6-1, and the yield was 27%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M6 was MS(ASAP)=1029.

[0122] Example 7 Organic compound M7( [ka] ) synthesis The synthetic route of organic compound M7 is as follows. [ka]

[0123] The specific synthesis procedure for the organic compound M7 is as follows.

[0124] Synthesis of intermediate M7-2 Following the synthesis method of compound M1-3, compounds M1-1 and M1-2 were replaced with compounds M7-1 and M2-2, respectively, with a yield of 74%.

[0125] Synthesis of intermediate M7-3 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M7-2 and M3-6, respectively, with a yield of 65%.

[0126] Synthesis of compound M7 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M7-3, and the yield was 30%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M7 was MS(ASAP)=1070.

[0127] Example 8 Organic compound M8( [ka] ) synthesis The synthetic route of organic compound M8 is as follows. [ka]

[0128] The specific synthesis procedure for the organic compound M8 is as follows.

[0129] Synthesis of intermediate M8-2 Following the synthesis method of compound M1-3, compounds M1-1 and M1-2 were replaced with compounds M5-1 and M2-2, respectively, with a yield of 76%.

[0130] Synthesis of intermediate M8-3 Following the synthesis method of compound M2-4, compound M2-3 was replaced with compound M8-2, and the yield was 70%.

[0131] Synthesis of compound M8 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M8-3, and the yield was 26%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M8 was MS(ASAP)=1160.

[0132] Example 9 Organic compound M9( [ka] ) synthesis The synthetic route of organic compound M9 is as follows. [ka]

[0133] The specific synthesis procedure for the organic compound M9 is as follows.

[0134] Synthesis of intermediate M9-2 Following the synthesis method of compound M1-3, compounds M1-1 and M1-2 were replaced with compounds M9-1 and M2-2, respectively, with a yield of 75%.

[0135] Synthesis of intermediate M9-3 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M9-2 and M3-6, respectively, with a yield of 66%.

[0136] Synthesis of compound M9 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M9-3, and the yield was 27%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M1 was MS(ASAP)=1086.

[0137] Example 10 Organic compound M10( [ka] ) synthesis The synthetic route of organic compound M10 is as follows. [ka]

[0138] The specific synthesis procedure for the organic compound M10 is as follows.

[0139] Synthesis of intermediate M10-2 Following the synthesis method of compound M1-3, compound M1-1 was replaced with compound M10-1, and the yield was 72%.

[0140] Synthesis of intermediate M10-5 Under a nitrogen atmosphere, compound M10-3 (39.6 g, 100 mmol), compound M10-4 (12.7 g, 100 mmol), tetrakis(triphenylphosphine)palladium (3.3 g, 3 mmol), potassium carbonate (20.6 g, 150 mmol), and 200 mL of toluene were added to a 500 mL three-neck flask, heated to 110 °C with stirring, and reacted for 12 hours. After the reaction was completed, the mixture was cooled to room temperature and suction filtered. The filtrate was collected and most of the solvent was removed by rotary evaporation. The filtrate was dissolved in dichloromethane and washed three times with water. The organic solution was collected, mixed with silica gel, and purified by column chromatography in a 70% yield.

[0141] Synthesis of intermediate M10-6 Following the synthesis method of compound M1-6, compound M1-4 was replaced with compound M10-5, with a yield of 61%.

[0142] Synthesis of intermediate M10-7 Following the synthesis method of compound M1-8, compound M1-6 was replaced with compound M10-6, with a yield of 54%.

[0143] Synthesis of intermediate M10-8 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M10-2 and M10-7, respectively, with a yield of 63%.

[0144] Synthesis of compound M10 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M10-8, and the yield was 26%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M10 was MS(ASAP)=1055.

[0145] Example 11 Organic compound M11( [ka] ) synthesis The synthetic route of the organic compound M11 is as follows. [ka]

[0146] The specific synthesis procedure for the organic compound M11 is as follows.

[0147] Synthesis of intermediate M11-1 Following the synthesis method of compound M1-8, compound M1-7 was replaced with compound M9-2, with a yield of 52%.

[0148] Synthesis of intermediate M11-2 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M8-2 and M11-1, respectively, with a yield of 62%.

[0149] Synthesis of compound M11 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M11-2, and the yield was 25%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M11 was MS(ASAP)=1176.

[0150] Example 12 Organic compound M12( [ka] ) synthesis The synthetic route of organic compound M12 is as follows. [ka]

[0151] The specific synthesis procedure for the organic compound M12 is as follows.

[0152] Synthesis of intermediate M12-2 Following the synthesis method of compound M1-3, compound M1-1 was replaced with compound M12-1, and the yield was 70%.

[0153] Synthesis of intermediate M12-5 Following the synthesis method of compound M10-5, compounds M10-4 and 10-3 were replaced with compounds M12-3 and M12-4, respectively, with a yield of 66%.

[0154] Synthesis of intermediate M12-7 Under a nitrogen atmosphere, compound M12-5 (20.6 g, 60 mmol), compound M12-6 (9 g, 60 mmol), CuI (0.57 g, 3 mmol), potassium carbonate (13.8 g, 100 mmol), and 150 mL of dimethylformamide were added to a 500 mL two-neck flask, heated to 110 °C, and stirred for 2 hours. The reaction mixture was then cooled to room temperature and rotary evaporated to remove most of the solvent. The mixture was dissolved in dichloromethane and washed three times with water. The organic solution was collected, mixed with silica gel, and purified by column chromatography in a 62% yield.

[0155] Synthesis of intermediate M12-8 Under a nitrogen atmosphere, intermediate M12-7 (12.4 g, 30 mmol), M1-5 (4.5 g, 30 mmol), Pd2(dba)3 (1.66 g, 1.8 mmol), tri-tert-butylphosphine (0.72 g, 3.6 mmol), sodium tert-butoxide (5.5 g, 60 mmol), and 100 mL of anhydrous toluene were added to a 350 mL two-neck flask, heated to 90 °C, and stirred for 6 h. The reaction was then cooled to room temperature and quenched by adding water. The reaction mixture was rotary evaporated to remove most of the solvent, dissolved in dichloromethane, and washed three times with water. The organic solution was collected, mixed with silica gel, and purified by column chromatography in a 65% yield.

[0156] Synthesis of intermediate M12-9 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M12-2 and M12-8, respectively, with a yield of 64%.

[0157] Synthesis of compound M12 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M12-9, and the yield was 31%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M12 was MS(ASAP)=971.

[0158] Example 13 Organic compound M13( [ka] ) synthesis The synthetic route of organic compound M13 is as follows. [ka]

[0159] The specific synthesis procedure for the organic compound M13 is as follows.

[0160] Synthesis of intermediate M13-2 Following the synthesis method of compound M3-3, compound M3-1 was replaced with compound M13-1, and the yield was 80%.

[0161] Synthesis of intermediate M13-3 Following the synthesis method of compound M1-3, compound M1-1 was replaced with compound M13-2, with a yield of 72%.

[0162] Synthesis of intermediate M13-5 Under a nitrogen atmosphere, compound M13-4 (35.2 g, 100 mmol) and 100 mL of anhydrous tetrahydrofuran solvent were added to a 500 mL three-neck flask, stirred to dissolve, and cooled to -78°C. 100 mmol of n-butyllithium was slowly added dropwise and allowed to react for 2 hours. 150 mmol of deuterated water was added all at once, and the reaction solution was slowly warmed to room temperature. Stirring was continued and the reaction was allowed to continue for 4 hours. After the reaction was completed, the reaction solution was rotary evaporated to remove most of the solvent, dissolved in dichloromethane, and washed three times with water. The organic solution was collected and mixed with silica gel and purified by column chromatography. The yield was 67%.

[0163] Synthesis of intermediate M13-6 Following the synthesis method of compound M12-7, compound M12-5 was replaced with compound M13-5, with a yield of 62%.

[0164] Synthesis of intermediate M13-7 Following the synthesis method of compound M12-8, compound M12-7 was replaced with compound M13-6, with a yield of 66%.

[0165] Synthesis of intermediate M13-8 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M13-3 and M13-7, respectively, with a yield of 63%.

[0166] Synthesis of compound M13 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M13-8, and the yield was 32%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M13 was MS(ASAP)=841.

[0167] Example 14 Organic compound M14( [ka] ) synthesis The synthetic route of organic compound M14 is as follows. [ka]

[0168] The specific synthesis procedure for the organic compound M14 is as follows.

[0169] Synthesis of intermediate M14-3 Following the synthesis method of compound M12-7, compounds M12-5 and M12-6 were replaced with M14-1 and M14-2, respectively, with a yield of 64%.

[0170] Synthesis of intermediate M14-4 Following the synthesis method of compound M12-8, compound M12-7 was replaced with compound M14-3, with a yield of 64%.

[0171] Synthesis of intermediate M14-5 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M7-2 and M14-4, respectively, with a yield of 65%.

[0172] Synthesis of compound M14 Following the synthesis method of compound M1, compound M1-9 was replaced with compound M14-5, with a yield of 31%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M14 was MS(ASAP)=938.

[0173] Example 15 Organic compound M15( [ka] ) synthesis The synthetic route of organic compound M15 is as follows. [ka]

[0174] The specific synthesis procedure for the organic compound M15 is as follows.

[0175] Synthesis of intermediate M15-2 Following the synthesis method of compound M1-3, compound M1-1 was replaced with compound M15-1, and the yield was 73%.

[0176] Synthesis of intermediate M15-4 Following the synthesis method of compound M12-7, compound M12-5 was replaced with compound M15-3, with a yield of 65%.

[0177] Synthesis of intermediate M15-6 Following the synthesis method of compound M12-8, compounds M12-7 and M12-1-5 were replaced with compounds M15-4 and M15-5, respectively, with a yield of 67%.

[0178] Synthesis of intermediate M15-7 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M15-2 and M15-6, respectively, with a yield of 68%.

[0179] Synthesis of compound M15 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M15-7, and the yield was 33%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M15 was MS(ASAP)=1064.

[0180] Example 16 Organic compound M16( [ka] ) synthesis The synthetic route of organic compound M16 is as follows. [ka]

[0181] The specific synthesis procedure for the organic compound M16 is as follows.

[0182] Synthesis of intermediate M16-2 Following the synthesis method of compound M1-3, compound M1-1 was replaced with compound M16-1, and the yield was 72%.

[0183] Synthesis of intermediate M16-5 Following the synthesis method of compound M12-7, compounds M12-6 and M12-5 were replaced with compounds M16-3 and M16-4, respectively, with a yield of 67%.

[0184] Synthesis of intermediate M16-6 Following the synthesis method of compound M12-8, compound M12-7 was replaced with compound M16-5, with a yield of 62%.

[0185] Synthesis of intermediate M16-7 Following the synthesis method of compound M1-9, compounds M1-3 and M1-8 were replaced with compounds M16-2 and M16-6, respectively, with a yield of 64%.

[0186] Synthesis of compound M16 According to the synthesis method of compound M1, compound M1-9 was replaced with compound M16-7, and the yield was 33%. The atmospheric pressure solid phase analytical probe mass spectrometry (ASAP-MS) result of organic compound M16 was MS(ASAP)=913.

[0187] An exemplary fabrication procedure for the light-emitting device provided by the present invention is as shown in the following Illustrative Example 17.

[0188] Example 17 In this example, the procedure for fabricating a light-emitting device having an anode (ITO) / hole injection layer (40 nm) / hole transport layer (100 nm) / light-emitting layer (host material: 3% (mass ratio) guest material) (50 nm) / electron transport layer (25 nm) / cathode (LiQ (1 nm) / Al (150 nm)) is as follows.

[0189] a. Cleaning of conductive glass substrates When first used, it can be cleaned with various solvents, such as chloroform, ketones, isopropanol, etc., followed by ultraviolet ozone plasma treatment.

[0190] b) A hole injection layer (40 nm), a hole transport layer (100 nm), an emitting layer (50 nm), and an electron transport layer (25 nm) were deposited in this order under high vacuum (1 × 10 -6 The films are then thermally evaporated at 1000 K (1000 mbar).

[0191] c, cathode LiQ (1 nm) / Al (150 nm) was placed under high vacuum (1 × 10 -6 The film was thermally evaporated at 1000 K (mbar).

[0192] d. Packaging The device is packaged with UV-curable resin in a nitrogen glove box.

[0193] In this example, the guest materials are organic compounds M1 to M16 for forming light-emitting elements 1 to 16, and Ref-1 for forming comparative element 1, respectively.

[0194] The structural formula of Ref-1 is: [ka] is.

[0195] In the light-emitting elements 1 to 16 and the comparative element 1, The structural formula of the material of the hole injection layer is: [ka] is.

[0196] The structural formula of the material of the hole transport layer is: [ka] is.

[0197] The structural formula of the host material in the light-emitting layer is: [ka] is.

[0198] The structural formula of the material of the electron transport layer is: [ka] is.

[0199] The structural formula of LiQ is: [ka] is.

[0200] In this example, external quantum efficiency (EQE) and luminescence lifetime tests (T90@1000nits, meaning the time it takes for the tested device to decay from 1000 nits to 900 nits) were performed on light-emitting elements 1 to 16 and comparative element 1, and the results obtained are shown in Table 1.

[0201] [Table 1]

[0202] From the data in Table 1, it can be seen that the external quantum efficiency and luminescence lifetime of the comparative element 1 are set as reference values ​​of 1, and that the external quantum efficiency and luminescence lifetime of the light-emitting elements 1 to 16 are significantly improved and the luminescence lifetime is also effectively extended. This indicates that the introduction of amine substituents into key positions strengthens the resonance effect and spatial effect of the organic compound, improves the performance of the guest material, and effectively improves the luminescence efficiency and luminescence lifetime of the light-emitting element.

[0203] The light-emitting device disclosed in the embodiments of the present invention uses an amino group-containing organic compound, and the organic compound has an amino group as well as a heterocycle, which enhances the resonance effect of the material used in the light-emitting device, improves the performance of the material, and increases the luminous efficiency and luminous life of the light-emitting device.

[0204] An embodiment of the present invention further discloses a display panel including any of the light-emitting elements described above.

[0205] The display panel further includes an array substrate located on one side of the light emitting device, and a package layer located on a side of the light emitting device away from the array substrate and covering the light emitting device. The display panel further includes a polarizer layer located on a side of the package layer away from the light emitting device, and a cover plate layer located on a side of the polarizer layer away from the light emitting device. Here, the polarizer layer may be replaced with a color film layer, and the color film layer may include a plurality of color resistors and black matrices located on both sides of the color resistors.

[0206] The display panel disclosed in the embodiments of the present invention uses a light-emitting element that uses an amino group-containing organic compound. By having the amino group in the organic compound along with a heterocycle, the resonance effect of the material used in the light-emitting element is strengthened, the performance of the material is improved, the light-emitting efficiency of the light-emitting element is improved, and the light-emitting life of the light-emitting element is extended.

[0207] The embodiments of the present invention disclose an organic compound, a light-emitting device, and a display panel, and the organic compound has a structure represented by general formula (1). [ka] The present invention uses an amino group-containing organic compound, which has an amino group in addition to a heterocycle, thereby enhancing the resonance effect of the material used in the light-emitting device, improving the performance of the material, and increasing the luminous efficiency and luminous life of the light-emitting device.

[0208] The organic compound, light-emitting device, and display panel provided in the embodiments of the present invention have been described in detail above. This specification uses specific examples to explain the principles and embodiments of the present invention. The explanation of the above examples is intended merely to aid in understanding the method of the present invention and its central concept. Furthermore, those skilled in the art can make modifications to the specific embodiments and application scope based on the concept of the present invention. In short, the contents of this specification should not be understood as limiting the present invention.

Claims

1. A structure represented by general formula (1): 【Chemistry 1】 wherein Z is CR １ R ２ , N.R. ３ , O or S; X is O or NR ４ is selected from R １ ~R ４ are each independently selected at each occurrence from a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, a substituted or unsubstituted aromatic group having 6 to 29 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 26 to 36 carbon atoms; R １ , R ２ may or may not be linked to each other to form a ring, Ar １ is selected from H, D, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, and a substituted or unsubstituted aromatic group having 6 to 20 carbon atoms; Ar ２ ~Ar ３ are each independently selected from substituted or unsubstituted aromatic groups having 7 to 18 carbon atoms; Ar 4 is selected from substituted or unsubstituted aromatic groups having 6 to 31 carbon atoms; Ar 5 to Ar ６ are each independently selected from a substituted or unsubstituted aromatic group having 6 to 31 carbon atoms and a substituted or unsubstituted heteroaromatic group having 6 to 26 carbon atoms, and is used as a guest material.

2. A structure represented by any one of general formulas (2) to (11): 【Chemistry 2】 2. The organic compound according to claim 1, wherein

3. Having a structure represented by general formula (12), 【Transformation 3】 wherein Y is selected from CR 5 R 6 , NR 7 , O or S; R 5 to R 7 in each occurrence are independently selected from a substituted or unsubstituted methyl group, a substituted or unsubstituted aromatic group having 6 to 10 carbon atoms; R 5 and R 6 may be bonded to each other to form a ring or may not form a ring; Ar 7 to Ar 8 are each independently selected from substituted or unsubstituted aromatic groups having 6 to 10 carbon atoms; 2. The organic compound according to claim 1, wherein Ar9 is selected from substituted or unsubstituted phenyl groups.

4. R 5 to R 7 at each occurrence are each independently selected from a methyl group and a substituted or unsubstituted phenyl group; 4. The organic compound according to claim 3, wherein Ar 7 to Ar 8 are each independently selected from the group consisting of a methyl group, a substituted or unsubstituted phenyl group, and a substituted or unsubstituted naphthyl group.

5. Having a structure represented by general formula (13), 【Chemistry 4】 In the formula, A represents CR 9 R 10 , NR 11 , O or S; n represents an integer of 0 to 4; R 8 to R 11 at each occurrence are each independently selected from a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms and a substituted or unsubstituted aromatic group having 6 to 10 carbon atoms; The organic compound according to claim 1, characterized in that when n is equal to 0, R 9 and R 10 are bonded to each other to form a ring or not to form a ring, and when n is 1 or more, R 8 and R 9 and / or R 10 are bonded to each other to form a ring or not to form a ring.

6. Having a structure represented by general formula (14), 【Transformation 5】 In the formula, Ar 10 to Ar 11 are each independently selected from a methyl group, a substituted or unsubstituted aromatic group having 6 to 18 carbon atoms, and a substituted or unsubstituted heteroaromatic group having 5 to 13 carbon atoms; 2. The organic compound according to claim 1, wherein Ar12 is selected from substituted or unsubstituted phenyl groups.

7. The organic compound according to claim 6, wherein Ar 10 to Ar 11 are each independently selected from a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group.

8. Ar １ is selected from H, D, methyl, isopropyl, tertiary butyl, tertiary amyl, substituted or unsubstituted phenyl, substituted or unsubstituted naphthyl, substituted or unsubstituted dibenzofuran, substituted or unsubstituted dibenzothiophene, substituted or unsubstituted fluorenyl, substituted or unsubstituted carbazolyl, and substituted or unsubstituted amino; Ar ２ ~Ar ３ are each independently selected from a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group; Ar ４ ~Ar ６ are each independently selected from a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzofuran, a substituted or unsubstituted dibenzothiophene, a substituted or unsubstituted fluorenyl group, and a substituted or unsubstituted carbazolyl group; R １ ~R ４ and each independently are selected from a methyl group and a substituted or unsubstituted phenyl group.

9. 2. The organic compound according to claim 1, characterized in that it is selected from the following compounds: 【Chemical Engineering 6A】 【Chemistry 6B】 【Chemical 6C】 【6D Transformation】 [Transformation 6E] 【Chemical 6F】 [6G] 【Chemical Formula 6H】 【Chemical 6I】

10. a pair of electrodes including a first electrode and a second electrode; an organic functional layer located between the first electrode and the second electrode; Including, A light-emitting device, wherein the material of the organic functional layer comprises one or more of the organic compounds according to claim 1 .

11. The light-emitting device according to claim 10, wherein the organic functional layer includes at least an emitting layer, the emitting layer includes a host material and a guest material, and the guest material is one or more of the organic compounds according to claim 1.

12. A display panel comprising the light-emitting element according to claim 10 .

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