Amine compound and its application

Abstract

The present invention belongs to the technical field of organic electroluminescence, and specifically relates to an amine compound and its application in organic electroluminescent materials and light-emitting elements. When the amine compound of the present invention is used as an electroluminescent material in an organic electroluminescent element, the organic electroluminescent element can achieve high efficiency, low driving voltage and long life because the carrier mobility of the amine compound is greater than that of previous materials, the amine compound has high internal quantum efficiency, excellent amorphous property and stable film state.

Description

Technical Field

[0001] The invention belongs to the technical field of organic electroluminescence, and in particular relates to an amino compound and application thereof in organic electroluminescent materials and light-emitting elements. Background Art

[0002] Organic light-emitting diodes (OLEDs), also known as organic electroluminescent devices, are a technology that uses organic materials to emit light through carrier injection and recombination under the action of an electric field. It can convert electrical energy into light energy through organic light-emitting materials, including passive-driven OLEDs (PMOLEDs) and active-driven OLEDs (AMOLEDs). OLEDs are a new generation of display technology after cathode ray tubes (CRTs) and liquid crystal displays (LCDs), and are known as fantastic display technologies. OLEDs have also shown good development prospects in communication terminals, military fields, and flexible displays. However, compared with other display technologies, OLEDs have been developed for a short time, and the current theoretical system for organic electroluminescent display technology is still not comprehensive and systematic. This field is also full of opportunities and challenges, such as poor device efficiency, high production requirements and costs, short device life, and poor stability. These problems still need to be solved.

[0003] One of the key factors affecting the efficiency of OLED devices is the injection and recombination process of carriers in the device. Studies have found that by balancing the carriers, the device efficiency can be effectively improved. However, the balance of carriers is difficult to control, which affects the exciton recombination luminescence of the light-emitting layer, resulting in low device efficiency. It is currently believed that the transmission rate of holes in OLED devices is much higher than the transmission rate of electrons. Therefore, the development of electron transport materials with high transmission rates is an effective way to improve the luminous efficiency of the device and has important research significance. Some common electron transport materials, such as metal organic complexes, have good film-forming properties and excellent electron transport properties; quinoline materials have low reduction potential values, good mechanical properties and high thermal stability; triazine compounds have the advantages of excellent heat resistance and high electron affinity potential energy; oxadiazole molecules have the advantages of excellent chemical stability, high electron transfer rate, reduced starting voltage, and good thermal stability.

[0004] Oxazole and oxadiazole have similar structures and both have electron-deficient properties, but oxazole-containing hole materials and capping layer materials are not common, and oxazole structures have not received much attention in optoelectronic materials. Previously, studies have found that by functionalizing them, their properties as hole materials and capping layer materials can be studied, filling the scientific research blind spot of oxazole as a functional material and laying the foundation for future scientific research.

[0005] In view of the above reasons, the present invention is proposed. Summary of the invention

[0006] In order to solve the above problems existing in the prior art, the present invention provides an amino compound, an organic electroluminescent material, a light-emitting element and a consumer product.

[0007] The first object of the present invention is to provide an amino compound.

[0008] The second object of the present invention is to provide an organic electroluminescent material.

[0009] The third object of the present invention is to provide an organic electroluminescent element.

[0010] The fourth object of the present invention is to provide a consumer product.

[0011] In order to achieve the above object, the present invention adopts the following technical solution:

[0012] An amino compound, the general structural formula of the amino compound is shown in formula (I):

[0013]

[0014] Among them, R 1 , R 2 Each is independently selected from substituted or unsubstituted C6 to C 50 Aryl, substituted or unsubstituted C2~C 50 Heteroaryl, substituted or unsubstituted C6~C 50 Arylamine, substituted or unsubstituted C5~C 50 The group consisting of arylsilyl groups;

[0015] R 3 , R 4 , R 5 , R 6 are independently selected from hydrogen, deuterium, cyano, halogen atoms, substituted or unsubstituted C1-C 30 Alkyl, substituted or unsubstituted C3~C 30 Cycloalkyl, substituted or unsubstituted C6~C 50 Aryl, substituted or unsubstituted C2~C 50 Heteroaryl, substituted or unsubstituted C6~C 50 Arylamine, substituted or unsubstituted C1~C 30 Alkylsilyl, substituted or unsubstituted C5~C 50 A group consisting of arylsilyl groups, any two or more adjacent R 3 , R 4 , R 5 , R 6They may be arbitrarily joined or fused to form a substituted or unsubstituted ring, and the formed ring may or may not contain heteroatoms N, O, S, P, B, Si or Se;

[0016] And, in R 1 , R 2 , R 3 , R 4 , R 5 , R 6 At least two of them are groups of formula (II), R 1 or R 2 When m is not 0, L 1 Not a single bond;

[0017]

[0018] Ar 1 ,Ar 2 Each independently selected from substituted or unsubstituted C6 to C 50 Aryl, substituted or unsubstituted C2~C 50 Heteroaryl, substituted or unsubstituted C6~C 50 A group consisting of arylamine groups;

[0019] L 1 Selected from single bonds, substituted or unsubstituted C6~C 50 Arylene, substituted or unsubstituted C2~C 50 The group consisting of heteroarylene;

[0020] m is an integer selected from 0 to 5;

[0021] Dashed lines represent the attachment sites of the groups.

[0022] Furthermore, the amino compound is selected from the group consisting of the following structures:

[0023]

[0024] Among them, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , L 1 ,Ar 1 and Ar 2 has the same meaning as defined above;

[0025] m and n are each independently selected from integers of 0 to 5; preferably, m and n are each independently selected from 0, 1 or 2;

[0026] Ar3 ,Ar 4 Each independently selected from substituted or unsubstituted C6 to C 50 Aryl, substituted or unsubstituted C2~C 50 Heteroaryl, substituted or unsubstituted C6~C 50 A group consisting of arylamine groups.

[0027] The alkyl group used in the present invention refers to a monovalent functional group obtained by removing one hydrogen atom from a straight or branched saturated hydrocarbon having a carbon number of 1 to 30. Non-limiting examples thereof include methyl, ethyl, propyl, isobutyl, sec-butyl, pentyl, isopentyl, hexyl, and the like;

[0028] The aryl group in the sense of the present invention contains 6 to 50 carbon atoms, and the heteroaryl group contains 2 to 50 carbon atoms and at least one heteroatom, provided that the total number of carbon atoms and heteroatoms is at least 5; the heteroatom is preferably selected from N, O or S. In this case, the two or more rings of the heteroaryl group can be attached to each other simply or in a condensed form, and further, can also include a condensed form with the aryl group. As non-limiting examples of aryl and heteroaryl groups, in particular, the following groups are selected: phenyl, naphthyl, anthracenyl, benzanthryl, phenanthrenyl, pyrenyl, yl, peryl, fluoranthene, tetraphenyl, pentacene, benzopyrenyl, biphenyl, phenylene, terphenyl, triphenyl, quadriphenyl, fluorenyl, spirobifluorenyl, dihydrophenanthryl, triphenylene, dihydropyrenyl, tetrahydropyrenyl, cis- or trans-indenofluorenyl, cis- or trans-indenocarbazolyl, indolecarbazolyl, benzofuranocarbazolyl, benzothiophenocarbazolyl, benzocarbazolyl, dibenzocarbazolyl, azadibenzo[g,Id]naphtho[2,1,8-cde]azulene, trimerized indenyl, isotrimerized indenyl, spirotrimerized indenyl, spiroisotrimerized indenyl, furanyl, benzofuranyl, isobenzofuranyl, dibenzofuranyl, thienyl, benzothienyl, isobenzothienyl, dibenzothienyl, pyrrolyl, indolyl, isoindolyl, carbazolyl, pyridinyl, quinolyl, isoquinolyl, acridinyl, phenanthridinyl, benzo[5,6]quinolyl, benzo[6,7]quinolyl, benzo[7,8]quinolyl, phenothiazinyl, phenoxazinyl, pyrazolyl, indazolyl, imidazolyl, benzimidazolyl, naphthoimidazolyl, phenanthroimidazolyl, pyridoimidazolyl, pyrazinoimidazolyl, quinoxalinoimidazolyl, oxazolyl, benzoxazolyl, naphthoxazolyl, anthrazolyl, phenanthroxazolyl, isoxazolyl, 1,2- Thiazolyl, 1,3-thiazolyl, benzothiazolyl, pyridazinyl, hexaazatriphenylene radical, benzopyridazinyl, pyrimidinyl, benzopyrimidinyl, quinoxalinyl, 1,5-diazaanthryl, 2,7-diazapyrenyl, 2,3-diazapyrenyl, 1,6-diazapyrenyl, 1,8-diazapyrenyl, 4,5-diazapyrenyl, 4,5,9,10-tetraazaperyl, pyrazinyl, phenazinyl, phenoxazinyl, phenothiazinyl, fluorescein ring radical, naphthyridinyl, azacarbazolyl, benzocarbolinyl, carbolinyl, phenanthrolinyl, 1,2,3-triazolyl, 1,2,4-triazolyl, benzotriazolyl, 1 ,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,3,5-triazinyl, 1,2,4-triazinyl, 1,2,3-triazinyl, tetrazolyl, 1,2,4,5-tetrazinyl, 1,2,3,4-tetrazinyl, 1,2,3,5-tetrazinyl, purinyl, pteridinyl, indolizinyl, quinazolinyl, benzothiadiazolyl or a group derived from a combination of these systems.

[0029] The "halogen" or "halogen atom" used in the present invention refers to a group selected from fluorine, chlorine, bromine or iodine.

[0030] Furthermore, the R 1 , R 2Each of the following is independently selected from substituted or unsubstituted phenyl, substituted or unsubstituted diphenyl, substituted or unsubstituted terphenyl, substituted or unsubstituted quaterphenyl, substituted or unsubstituted pyridyl, substituted or unsubstituted pyrimidinyl, substituted or unsubstituted naphthyl, substituted or unsubstituted phenanthryl, substituted or unsubstituted triphenylene, substituted or unsubstituted anthracenyl, substituted or unsubstituted benzanthryl, substituted or unsubstituted pyrenyl, substituted or unsubstituted substituted or unsubstituted peryl, substituted or unsubstituted fluoranthene, substituted or unsubstituted carbazolyl, substituted or unsubstituted fluorenyl, substituted or unsubstituted indolyl, substituted or unsubstituted benzofuranyl, substituted or unsubstituted benzothiophene, substituted or unsubstituted dibenzofuranyl, substituted or unsubstituted dibenzothiophene, substituted or unsubstituted triazine, or a group consisting of formula (II).

[0031] Furthermore, the R 3 , R 4 , R 5 , R 6 each independently selected from hydrogen, deuterium, a cyano group, a halogen atom, a substituted or unsubstituted phenyl group, a substituted or unsubstituted diphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted quaterphenyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted pyrimidyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted anthracenyl group, a substituted or unsubstituted benzanthryl group, a substituted or unsubstituted pyrenyl group, a substituted or unsubstituted substituted or unsubstituted peryl, substituted or unsubstituted fluoranthene, substituted or unsubstituted carbazolyl, substituted or unsubstituted fluorenyl, substituted or unsubstituted indolyl, substituted or unsubstituted benzofuranyl, substituted or unsubstituted benzothiophene, substituted or unsubstituted dibenzofuranyl, substituted or unsubstituted dibenzothiophene, substituted or unsubstituted triazine, or a group consisting of formula (II).

[0032] Furthermore, the Ar 1 ,Ar 2 Each of the following is independently selected from substituted or unsubstituted phenyl, substituted or unsubstituted diphenyl, substituted or unsubstituted terphenyl, substituted or unsubstituted quaterphenyl, substituted or unsubstituted pyridyl, substituted or unsubstituted naphthyl, substituted or unsubstituted phenanthryl, substituted or unsubstituted triphenylene, substituted or unsubstituted anthracenyl, substituted or unsubstituted benzanthryl, substituted or unsubstituted pyrenyl, substituted or unsubstituted The invention also comprises a group consisting of a substituted or unsubstituted perylene group, a substituted or unsubstituted fluoranthene group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted indolyl group, a substituted or unsubstituted benzofuranyl group, a substituted or unsubstituted benzothiophene group, a substituted or unsubstituted dibenzofuranyl group, and a substituted or unsubstituted dibenzothiophene group.

[0033] Furthermore, the Ar 3 ,Ar 4 Each of the following is independently selected from substituted or unsubstituted phenyl, substituted or unsubstituted diphenyl, substituted or unsubstituted terphenyl, substituted or unsubstituted quaterphenyl, substituted or unsubstituted pyridyl, substituted or unsubstituted naphthyl, substituted or unsubstituted phenanthryl, substituted or unsubstituted triphenylene, substituted or unsubstituted anthracenyl, substituted or unsubstituted benzanthryl, substituted or unsubstituted pyrenyl, substituted or unsubstituted The invention also comprises a group consisting of a substituted or unsubstituted perylene group, a substituted or unsubstituted fluoranthene group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted indolyl group, a substituted or unsubstituted benzofuranyl group, a substituted or unsubstituted benzothiophene group, a substituted or unsubstituted dibenzofuranyl group, and a substituted or unsubstituted dibenzothiophene group.

[0034] Heteroalkyl in the sense of the present invention means that the hydrogen atom or -CH2- on the alkyl group is replaced by at least one heteroatom, and the heteroatom is selected from halogen, nitrile, N, O, S or silicon, as non-limiting examples, there are difluoromethyl, trifluoromethyl, trifluoroethyl, pentafluoroethyl, nitrile, acetonitrile, methoxymethyl, methoxyethyl, trimethylsilyl, triisopropylsilyl, etc. Haloalkyl means that the hydrogen atom on the alkyl group is partially or fully replaced by halogen, as non-limiting examples, there are fluorotoluene, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, trifluoroethyl, pentafluoroethyl, etc.

[0035] The alkenyl or alkynyl group used in the present invention contains at least two carbon atoms. As non-limiting examples, alkenyl or alkynyl is preferably taken to mean the following groups: cyclohexenyl, heptenyl, cycloheptenyl, octenyl, cyclooctenyl, ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl or octynyl.

[0036] The alkoxy and alkylthio groups used in the present invention are preferably alkoxy or alkylthio groups having 1 to 30 carbon atoms, and are considered to be methoxy, trifluoromethoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy, tert-butoxy, n-pentoxy, sec-pentoxy, 2-methylbutoxy, n-hexyloxy, cyclohexyloxy, n-heptyloxy, cycloheptyloxy, n-octyloxy, cyclooctyloxy, 2-ethylhexyloxy, pentafluoroethoxy and 2,2,2-trifluoroethoxy, methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio 4-(2-(4-(2-methyl-1-thio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1,4-dithio)-1

[0037] Generally speaking, the cycloalkyl and cycloalkenyl groups according to the present invention can be cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptyl, and cycloheptenyl, wherein one or more -CH2- groups can be replaced by N, O or S to form heterocycloalkyl and heterocycloalkenyl groups, for example, one -CH2- group in the cyclopentyl group is replaced by O to form tetrahydrofuranyl, one -CH2- group in the cyclohexyl group is replaced by O to form tetrahydropyranyl, etc.; in addition, one or more hydrogen atoms can also be replaced by deuterium atoms, halogen atoms or nitrile groups.

[0038] The aryloxy group used in the present invention refers to a monovalent functional group represented by R'O-, wherein R' is an aryl group having a carbon number of 6 to 50. Non-limiting examples of such aryloxy groups include phenoxy, naphthoxy, biphenyloxy and the like.

[0039] The arylthio group used in the present invention refers to a monovalent functional group represented by R"S-, wherein R" is an aryl group having 6 to 50 carbon atoms. Non-limiting examples of such arylthio groups include phenylthio, naphthylthio, biphenylthio and the like.

[0040] The alkylsilyl used in the present invention refers to a silyl group substituted by an alkyl group having 1 to 30 carbon atoms, and the number of carbon atoms constituting the alkylsilyl group is at least 3. Non-limiting examples of the alkylsilyl group include trimethylsilyl and triethylsilyl. The arylsilyl group refers to an alkylsilyl group substituted by at least one aryl group having 6 to 50 carbon atoms, and non-limiting examples include phenyldimethylsilyl, naphthyldimethylsilyl, phenyldiethylsilyl, diphenylmethylsilyl, diphenylethylsilyl, triphenylsilyl, and the like.

[0041] "Alkylcarbonyl", "alkoxycarbonyl", "arylcarbonyl", "arylborylcarbonyl" and "alkylborylcarbonyl" in the sense of the present invention refer to a substituted carbonyl group (-COR*), wherein R* is preferably selected from the group consisting of alkyl, alkoxy, cycloalkyl, aryl, heteroaryl, arylboryl and alkylboryl.

[0042] The arylphosphino group used in the present invention refers to a diarylphosphino group substituted with an aryl group having 6 to 50 carbon atoms, and non-limiting examples of the arylphosphino group include diphenylphosphino group, di(4-trimethylsilylphenyl)phosphino group, etc. The aryloxyphosphino group is a diarylphosphino group in which the phosphorus atom is oxidized to the highest valence state.

[0043] The aryl boryl group used in the present invention refers to a diaryl boryl group substituted by an aryl group having 6 to 50 carbon atoms, and non-limiting examples of the aryl boryl group include diphenyl boryl and di(2,4,6-trimethylphenyl)boryl. The alkyl boryl group refers to a dialkyl boryl group substituted by an alkyl group having 1 to 30 carbon atoms, and non-limiting examples of the alkyl boryl group include di-tert-butyl boryl and diisobutyl boryl.

[0044] The arylalkyl group according to the present invention refers to an alkyl group in which at least one hydrogen atom of a straight or branched saturated hydrocarbon having 1 to 30 carbon atoms is substituted by an aryl group having 6 to 50 carbon atoms, and as non-limiting examples, may be phenylmethyl, diphenylmethyl, triphenylmethyl, 2-phenylethyl, 3-phenylpropyl, and the like.

[0045] The alkylaryl group according to the present invention refers to an aryl group having 6 to 50 carbon atoms in which at least one hydrogen atom is substituted by a straight-chain or branched saturated hydrocarbon having 1 to 30 carbon atoms. As non-limiting examples, it may be methylphenyl, dimethylphenyl, trimethylphenyl, tert-butylphenyl, isopropylphenyl, etc.

[0046] Preferably, the heteroaryl group is selected from the group consisting of the following groups shown in II-1 to II-13:

[0047]

[0048] in,

[0049] Z1 and Z2 are each independently selected from hydrogen, deuterium, halogen, hydroxyl, nitrile, nitro, amino, amidine, hydrazine, hydrazone, carboxyl or its carboxylate, sulfonic acid or its sulfonate, phosphoric acid or its phosphate, C1-C 40 Alkyl, C2-C 30 Alkenyl, C2-C 30 Alkynyl, C1-C 30 Alkoxy, C3-C 30 Cycloalkane, C3-C 30 Cycloalkene, substituted or unsubstituted C6-C50 Aryl, substituted or unsubstituted C6-C 50 Aryloxy, substituted or unsubstituted C6-C 50 Aryl sulfide, substituted or unsubstituted C6-C 50 Arylamine, or substituted or unsubstituted C2-C 50 The group consisting of heteroaryl;

[0050] x1 represents an integer from 1 to 4; x2 represents an integer from 1 to 3; x3 represents 1 or 2; x4 represents an integer from 1 to 6; x5 represents an integer from 1 to 5;

[0051] T1 means O, S or NAr ’ ;

[0052] Ar ’ Choose from C1~C 30 Alkyl, C1~C 30 Heteroalkyl, C3~C 30 Cycloalkyl, substituted or unsubstituted C6-C 50 Aryl, substituted or unsubstituted C6-C 50 Condensed ring aromatic group, substituted or unsubstituted C6-C 50 Arylamine, or substituted or unsubstituted C2-C 50 The group consisting of heteroaryl; preferably, Ar ’ is methyl, ethyl, phenyl, biphenyl or naphthyl;

[0053] Indicates the attachment site of a group.

[0054] Furthermore, the heteroaryl group is selected from the group consisting of groups represented by formulae II-1 to II-13.

[0055] The substituents of the substituted alkyl, substituted aryl, substituted heteroaryl, substituted arylamino, substituted fused aryl, substituted arylene, and substituted heteroarylene described in the present invention are each independently selected from at least one of the following groups: deuterium, halogen, cyano, carboxyl, nitro, hydroxyl, C1-C 30 Alkyl, C1-C 30 Halogenated alkyl, C2-C 30 Alkenyl, C2-C 30 Alkynyl, C1-C 30 Alkoxy, C1-C 30 Alkylthio, C3-C 30 Cycloalkyl, C3-C 30 Cycloalkenyl, 3- to 7-membered heterocycloalkyl, C6-C 50 Aryloxy, C6-C 50 Arylthio, unsubstituted or substituted with one or more C6-C 503- to 30-membered heteroaryl, unsubstituted or deuterated, one or more C1-C 30 C6-C substituted with at least one of an alkyl group and one or more 3- to 30-membered heteroaryl groups 50 Aryl, tri(C1-C 30 ) alkylsilyl, tri(C6-C 50 )Arylsilyl, di(C1-C 30 ) alkyl (C6-C 50 )Arylsilyl, C1-C 30 Alkyl di(C6-C 50 )Arylsilyl, C1-C 30 Alkylcarbonyl, C1-C 30 Alkoxycarbonyl, C6-C 50 Arylcarbonyl, di(C6-C 50 ) aryl borocarbonyl, di(C1-C 30 ) alkyl boron carbonyl, C1-C 30 Alkyl (C6-C 50 )Aryl boron carbonyl, C6-C 50 Aryl (C1-C 30 ) alkyl, and C1-C 30 Alkyl (C6-C 50 )aryl.

[0056] The arylene group in the present invention refers to a divalent functional group obtained by removing two hydrogen atoms from an aromatic hydrocarbon having a carbon number of 6 to 50. Non-limiting examples thereof include phenylene, naphthylene, phenanthrylene, anthrylene, fluorenylene, and spirobifluorenylene.

[0057] The heteroarylene or heteroarylene group in the present invention refers to a divalent functional group obtained by removing two hydrogen atoms from a heteroaromatic hydrocarbon having a carbon number of from 2 to 50; further, the heteroarylene or heteroarylene group of the present invention is selected from a divalent functional group obtained by removing two hydrogen atoms from a group represented by formulas II-1 to II-13, for example, as non-limiting examples, there are pyridylene, quinolylene, isoquinolylene, carbolylene, pyrimidylene, triazinylene, and the like.

[0058] According to the aforementioned arylene group and heteroarylene group as a divalent functional group connected to N, preferably, the L 1 Selected from a single bond or the group consisting of the following groups shown in III-1 to III-25:

[0059]

[0060]

[0061] Wherein, X is selected from O, S, Se, CR ’ R”、SiR’ R" or NAr ’ ;

[0062] Z 11 , Z 12 , Z 13 , Z 14 Each is independently selected from hydrogen, deuterium, a halogen atom, a hydroxyl group, a nitrile group, a nitro group, an amino group, an amidine group, a hydrazine group, a hydrazone group, a carboxyl group or a carboxylate thereof, a sulfonic acid group or a sulfonate thereof, a phosphoric acid group or a phosphate thereof, a C1-C 30 Alkyl, C2-C 30 Alkenyl, C2-C 30 Alkynyl, C1-C 30 Alkoxy, C3-C 30 Cycloalkane, C3-C 30 Cycloalkene, substituted or unsubstituted C6-C 50 Aryl, substituted or unsubstituted C6-C 50 Aryloxy, substituted or unsubstituted C6-C 50 aryl thioether group, or substituted or unsubstituted C2-C 50 The group consisting of heteroaryl;

[0063] y1 represents an integer of 1-4; y2 represents an integer of 1-6; y3 represents an integer of 1-3; y4 represents an integer of 1-5; y5 represents an integer of 1 or 2;

[0064] R ’ , R" are each independently selected from C1-C 30 Alkyl, C1-C 30 heteroalkyl, substituted or unsubstituted C6-C 50 Aryl, substituted or unsubstituted C6-C 50 Arylamine, or substituted or unsubstituted C2-C 50 The group consisting of heteroaryl groups, R ’ and R" may be optionally joined or fused to form one or more additional substituted or unsubstituted rings, containing or not containing one or more heteroatoms N, P, B, O or S in the formed rings; preferably, R ’ , R" is methyl, phenyl or fluorenyl;

[0065] Ar ’ Choose from C1-C 30 Alkyl, C1-C 30 Heteroalkyl, C3-C 30 Cycloalkyl, substituted or unsubstituted C6-C 50 Aryl, substituted or unsubstituted C6-C 50 Condensed ring aromatic group, substituted or unsubstituted C6-C 50Arylamine, or substituted or unsubstituted C2-C 50 The group consisting of heterocyclic aromatic groups; preferably, Ar ’ is methyl, ethyl, phenyl, biphenyl or naphthyl;

[0066] The dashed lines represent the attachment sites of the groups.

[0067] Preferably, X is selected from O or S.

[0068] Preferably, the L 1 Each is independently selected from a single bond or a group consisting of the following groups III-1 to III-15 and III-25:

[0069]

[0070] Preferably, the Z 11 , Z 12 , Z 13 , Z 14 Each is independently selected from the group consisting of hydrogen, deuterium, fluorine, and nitrile.

[0071] Furthermore, the amino compound is selected from one or more of the following structures C01 to C204:

[0072]

[0073]

[0074]

[0075]

[0076]

[0077]

[0078]

[0079]

[0080]

[0081] Wherein, G is selected from O, S, CR 7 R 8 or NAr 3 ;

[0082] The R 7 and R 8 are methyl, phenyl or fluorenyl respectively;

[0083] The Ar3 Selected from the group consisting of:

[0084]

[0085] As used herein, "combinations thereof" or "groups" means that one or more members of the applicable list are combined to form known or chemically stable arrangements that can be envisioned by one of ordinary skill in the art from the applicable list. For example, alkyl and deuterium atoms can be combined to form partially or fully deuterated alkyls; halogens and alkyls can be combined to form haloalkyl substituents, such as trifluoromethyl, etc.; and halogens, alkyls, and aryls can be combined to form haloaralkyls.

[0086] An organic electroluminescent material comprises the amino compound.

[0087] The organic electroluminescent material may be composed of the amino compound of the present invention alone, or may contain other compounds at the same time.

[0088] The amino compound of the present invention contained in the organic electroluminescent material of the present invention can be used as, but not limited to, a light-emitting layer material, a carrier transport layer material, a capping layer material or a charge generation layer material.

[0089] An organic electroluminescent device comprises a first electrode, a second electrode, a capping layer and at least one organic layer disposed between the first electrode and the second electrode, wherein the organic layer or the capping layer comprises the amino compound provided by the invention.

[0090] The organic electroluminescent device comprises a cathode, an anode and at least one light-emitting layer. In addition to these layers, it may also comprise other layers, for example, in each case, one or more hole injection layers, hole transport layers, hole blocking layers, electron transport layers, electron injection layers, exciton blocking layers, electron blocking layers and / or charge generation layers. An intermediate layer having, for example, an exciton blocking function may also be introduced between two light-emitting layers. However, it should be noted that each of these layers does not necessarily have to be present. The organic electroluminescent device described herein may comprise one light-emitting layer, or it may comprise multiple light-emitting layers. That is, a variety of light-emitting compounds capable of emitting light are used in the light-emitting layer. Preferably, a system with three light-emitting layers is provided, wherein the three layers can display blue, green and red light emission. If there is more than one light-emitting layer, then according to the present invention, at least one of these layers comprises an amino compound of the present invention.

[0091] Furthermore, the organic electroluminescent device according to the present invention does not include a separate hole injection layer and / or hole transport layer and / or hole blocking layer and / or electron transport layer, that is, the light-emitting layer is directly adjacent to the hole injection layer or the anode, and / or the light-emitting layer is directly adjacent to the electron transport layer or the electron injection layer or the cathode.

[0092] In the other layers of the organic electroluminescent device according to the invention, in particular in the hole transport layer and the capping layer and in the emitting layer, all materials can be used in the manner commonly used according to the prior art. A person skilled in the art will therefore be able to use all materials known about organic electroluminescent elements in combination with the emitting layer according to the invention without inventive effort.

[0093] Furthermore, preference is given to organic electroluminescent devices in which one or more layers are applied by means of a sublimation process, wherein the organic electroluminescent devices are deposited in a vacuum sublimation apparatus at temperatures below 10 -5 Pa, preferably less than 10 -6 The material is applied by vapor deposition at an initial pressure of 10 Pa. However, the initial pressure may also be even lower, for example below 10 -7 Pa.

[0094] Likewise preferred is an organic electroluminescent device in which one or more layers are applied by means of an organic vapor phase deposition method or by means of carrier gas sublimation, wherein at 10 -5 The material is applied at a pressure of between 1000 Pa and 1 Pa. A particular example of this method is the organic vapor jet printing method, in which the material is applied directly through a nozzle and is thus structured.

[0095] In addition, preferred organic electroluminescent devices are produced from solutions, for example by spin coating, or by any desired printing method, for example screen printing, flexographic printing, lithography, photoinduced thermography, thermal transfer, inkjet printing or nozzle printing, to produce one or more layers. Soluble compounds, for example by appropriate substitution of fused ring compounds of formula I. These methods are also particularly suitable for oligomers, dendrimers and polymers. Also possible are hybrid methods, in which, for example, one or more layers are applied from solution and one or more further layers are applied by vapor deposition.

[0096] These methods are generally known to those skilled in the art, and they can apply them to the organic electroluminescent element comprising the amine compound according to the present invention without inventive effort.

[0097] The present invention therefore also relates to a method for producing an organic electroluminescent device according to the invention, which applies at least one layer by means of a sublimation method and / or applies at least one layer by means of an organic vapor phase deposition method or by means of carrier gas sublimation and / or applies at least one layer from a solution by spin coating or by means of a printing method.

[0098] In addition, the present invention relates to compounds according to the invention comprising at least one indicated above. The same preferences as indicated above for organic electroluminescent devices apply to the compounds according to the invention. In particular, the compounds may also preferably comprise other compounds. Processing the compounds according to the invention from the liquid phase, for example by spin coating or by a printing method, requires formulations of the compounds according to the invention. These formulations may, for example, be solutions, dispersions or emulsions. For this purpose, a mixture of two or more solvents may preferably be used. Suitable and preferred solvents are, for example, toluene, anisole, o-xylene, m-xylene or p-xylene, methyl benzoate, mesitylene, tetralin, o-dimethoxybenzene, tetrahydrofuran, methyltetrahydrofuran, tetrahydropyran, chlorobenzene, dioxane, phenoxytoluene, in particular 3-phenoxytoluene, (-)-fennel, 1,2,3,5-tetramethylbenzene, 1,2,4,5-tetramethylbenzene, 1-methylnaphthalene, 2-methylbenzothiazole, 2-phenoxyethanol, 2-pyrrolidone, 3-methylanisole, 4-methylanisole, 3,4-dimethylanisole, 3,5-dimethylanisole, acetophenone, α-terpenes benzothiazole, butyl benzoate, isopropylbenzene, cyclohexanol, cyclohexanone, cyclohexylbenzene, decalin, dodecylbenzene, ethyl benzoate, indane, methyl benzoate, 1-methylpyrrolidone, p-cymene, phenethyl ether, 1,4-diisopropylbenzene, dibenzyl ether, diethylene glycol butyl methyl ether, triethylene glycol butyl methyl ether, diethylene glycol dibutyl ether, triethylene glycol dimethyl ether, diethylene glycol monobutyl ether, tripropylene glycol dimethyl ether, tetraethylene glycol dimethyl ether, 2-isopropylnaphthalene, pentylbenzene, hexylbenzene, heptylbenzene, octylbenzene, 1,1-bis(3,4-dimethylphenyl)ethane, or a mixture of these solvents.

[0099] Furthermore, the organic layer is selected from one or more of an electron transport layer, a hole blocking layer, an electron blocking layer, a hole transport layer, a hole injection layer, a light emitting layer and a charge generating layer.

[0100] Furthermore, the hole injection layer, hole transport layer, light-emitting layer, capping layer or charge generation layer comprises the amino compound of the present invention.

[0101] Furthermore, the hole injection layer, hole transport layer and capping layer contain the amino compound of the present invention.

[0102] Furthermore, the hole injection layer includes a dopant and a host material. Depending on the type of the dopant, the Fermi level of the element can also be changed. The hole injection layer can be doped with a p-type conductive dopant. As a non-limiting example, the p-type dopant includes a group consisting of the following compounds:

[0103]

[0104]

[0105] In addition, as dopant materials, they can be formed into a film alone, or used as a single layer formed by mixing with other materials, or as a stacked structure between layers formed by alone, between layers formed by mixing, or between layers formed by alone and layers formed by mixing.

[0106] In order to avoid concentration quenching, the p-type dopant material is preferably doped into the host material by co-evaporation in a range of 1 to 10% based on the weight of the hole injection layer.

[0107] Furthermore, the host material of the hole injection layer comprises the amino compound of the present invention.

[0108] Furthermore, the mass ratio of the dopant to the main material of the present invention is 1:99 to 50:50.

[0109] A consumer product made from the organic electroluminescent device, wherein the consumer product comprises the organic electroluminescent device provided by the present invention.

[0110] The consumer product described in the present invention can be one of the following products: flat panel displays, computer monitors, medical monitors, televisions, billboards, lights for interior or exterior lighting and / or signaling, heads-up displays, fully or partially transparent displays, flexible displays, laser printers, telephones, cellular phones, tablet computers, tablet phones, personal digital assistants (PDAs), wearable devices, laptop computers, digital cameras, video cameras, viewfinders, microdisplays with a diagonal of less than 2 inches, 3-D displays, virtual reality or augmented reality displays, vehicles, video walls comprising multiple displays tiled together, theater or stadium screens, light therapy devices and signage.

[0111] Compared with the prior art, the present invention has the following beneficial effects:

[0112] The amino compound of the present invention has a rigid structure such as benzoxazole or naphthoxazole, thereby improving the structural stability of the material. As for the compound represented by the general formula (I) of the present invention, in terms of spatial structure, it contains an oxazole group with strong electronic properties and contains at least two mutually crossed triarylamine groups, thereby avoiding free rotation of the groups, so that the material has a higher density and obtains a higher refractive index. At the same time, the material of the present invention has a higher glass transition temperature. The evaporation temperature of the material of the present invention under vacuum is generally less than 350° C., which not only ensures that the material does not decompose during long-term evaporation, but also reduces the deformation effect of the thermal radiation of the evaporation temperature on the evaporation mask, and is therefore suitable for use as a constituent material of an organic electroluminescent element.

[0113] The amino compound of the present invention is used in CPL and does not participate in the electron and hole transport of the component, but has very high requirements on the thermal stability, film crystallinity and light transmission of the material. As analyzed above, the T-shaped cross-benzothazole or naphthoxazole of the amino compound of the present invention is a rigid group, which improves the stability and glass transition temperature of the material and ensures that the material does not crystallize in the thin film state; the low evaporation temperature is the prerequisite for its application in mass production; the high refractive index is the most important factor that the amino compound of the present invention can be applied to CPL.

[0114] As for the application of the amino compound represented by the above general formula (I) of the present invention in an organic electroluminescent element, due to its deep HOMO energy level and high electron mobility, it can effectively block the transfer of holes or energy from the light-emitting layer to the electronic layer side, thereby improving the recombination efficiency of holes and electrons in the light-emitting layer, thereby improving the luminous efficiency and service life of the element.

[0115] Furthermore, in the present invention, after the CPL layer is formed by using the amino compound of the general formula (I), the light extraction efficiency of the organic electroluminescent element can be maximized.

[0116] In addition, in the present invention, with respect to an organic electroluminescent element that uses an amino compound represented by the above-mentioned general formula (I) as its constituent material in at least any one layer of the above-mentioned light-emitting layer or a stacked film having two or more light-emitting layers, since a compound having high carrier mobility, high internal quantum efficiency, excellent amorphous property and stable thin film state is used, an organic electroluminescent element with high efficiency, low driving voltage and long life can be realized. BRIEF DESCRIPTION OF THE DRAWINGS

[0117] In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings required for use in the embodiments or the description of the prior art will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the present invention. For ordinary technicians in this field, other drawings can be obtained based on these drawings without paying creative work.

[0118] Figure 1 A schematic diagram of an organic light-emitting device 100 is shown. The illustration is not necessarily drawn to scale. The device 100 may include a substrate 101, an anode 102, a hole injection layer 103, a hole transport layer 104, an electron blocking layer 105, a light-emitting layer 106, a hole blocking layer 107, an electron transport layer 108, an electron injection layer 109, a cathode 110, and a capping layer (CPL) 111. The device 100 may be manufactured by depositing the described layers in order.

[0119] Figure 2 Schematic diagram of an organic light-emitting device 200 showing two light-emitting layers. The device includes a substrate 201, an anode 202, a hole injection 203, a hole transport layer 204, a first light-emitting layer 205, an electron transport layer 206, a charge generation layer 207, a hole injection layer 208, a hole transport layer 209, a second light-emitting layer 210, an electron transport layer 211, an electron injection layer 212, and a cathode 213. The device 200 can be prepared by depositing the layers described in sequence. Because the most common OLED device has one light-emitting layer, and the device 200 has a first light-emitting layer and a second light-emitting layer, the light emission peaks of the first light-emitting layer and the second light-emitting layer can be overlapping, cross-overlapping, or non-overlapping. In the corresponding layers of the device 200, materials similar to those described with respect to the device 100 can be used. Figure 2 An example of how to add some layers from the structure of device 100 is provided. DETAILED DESCRIPTION

[0120] To make the purpose, technical solution and advantages of the present invention clearer, the technical solution of the present invention will be described in detail below. Obviously, the described embodiments are only part of the embodiments of the present invention, rather than all the embodiments. Based on the embodiments of the present invention, all other implementation methods obtained by ordinary technicians in this field without creative work belong to the scope of protection of the present invention.

[0121] In the present invention, the preparation methods are conventional methods unless otherwise specified. The raw materials used can be obtained from public commercial channels unless otherwise specified, and the percentages are mass percentages unless otherwise specified. In the series of novel organic compounds provided by the present invention, all reactions are carried out under well-known suitable conditions, and some involve simple organic preparations, such as the preparation of phenylboronic acid derivatives, which can be synthesized by skilled operation skills and are not described in detail in the present invention.

[0122] Any range described in the present invention includes the end value and any numerical value between the end values ​​and any sub-range formed by the end value or any numerical value between the end values.

[0123] The test instruments and methods for testing the performance of OLED materials and components in the following embodiments are as follows:

[0124] OLED component performance testing conditions:

[0125] Brightness and chromaticity coordinates: tested using a spectral scanner PhotoResearch PR-715;

[0126] Current density and lighting voltage: tested using Keithley 2420 digital source meter;

[0127] Power efficiency: tested using NEWPORT 1931-C;

[0128] Life test: Use LTS-1004AC life test device.

[0129] Example 1

[0130] The preparation method of compound C07 comprises the following steps:

[0131] Step 1: Preparation of compound Int-1

[0132]

[0133] Under nitrogen protection, 20.0 mmol of o-iodobenzonitrile was dissolved in 80 mL of dry THF, cooled to -10°C, and 22.0 mmol of p-bromophenyllithium THF solution was added dropwise. The reaction was stirred for 2 hours, and 100 mL of 1 M dilute hydrochloric acid aqueous solution was added. The mixture was extracted with ethyl acetate, and the organic phase was collected, dried, and filtered. The filtrate was concentrated and dried under reduced pressure, and separated and purified by silica gel column to obtain compound Int-1 as a yellow solid. The yield was 89%.

[0134] Step 2: Preparation of compound Int-2

[0135]

[0136] Under nitrogen protection, 20.0 mmol of Int-1, 22.0 mmol of p-bromobenzamidopropyne, 60 mL of acetonitrile and 6 mL of triethylamine were mixed, 1.0 mmol of cuprous iodide and 1.0 mmol of PdCl2(PPh3)2 catalyst were added, the temperature was raised to reflux and stirred for 2 hours, cooled to room temperature, 100 mL of saturated aqueous ammonium chloride solution was added, extracted with ethyl acetate, the organic phase was collected, dried, filtered, the filtrate was concentrated and dried under reduced pressure, and separated and purified by silica gel column to obtain compound Int-2 as a yellow solid, yield: 65%.

[0137] Step 3: Preparation of compound Int-3

[0138]

[0139] Under nitrogen protection, 20.0 mmol of Int-2 prepared in the previous step, 2.0 mmol of silver trifluoroacetate, 50 mL of 1,2-dichloroethane and 20.0 mmol of water were mixed, stirred and reacted at room temperature for 2 hours, and then 40.0 mmol of p-toluenesulfonic acid was added, the temperature was raised to 85°C and stirred and reacted for 1 hour, cooled to room temperature, 50 mL of saturated sodium bicarbonate aqueous solution was added, extracted with ethyl acetate, the organic phase was collected, dried, filtered, the filtrate was concentrated and dried under reduced pressure, and separated and purified by silica gel column to obtain compound Int-3 as a yellow solid with a yield of 54%.

[0140] Step 4: Preparation of compound C07

[0141]

[0142] Under nitrogen protection, 20.0mmol of Int-3 (reactant 1) prepared in the previous step, 44.0mmol of sub-1 (reactant 2), 60.0mmol of sodium tert-butoxide, 2.0mmol of cuprous iodide, 0.2mmol of Pd2(dba)3 and 80mL of toluene were mixed, and then 0.4mmol of 10% tri-tert-butylphosphonium toluene solution was added. The temperature was raised to reflux and stirred for reaction for 15 hours, then cooled to room temperature, 50mL of water was added, the organic phase was separated, the aqueous phase was extracted with toluene, the organic phase was dried, filtered, the filtrate was concentrated and dried under reduced pressure, and separated and purified by silica gel column to obtain compound C07 as a white solid with a yield of 84%. MS (TOF): m / z 808.3344 [M+H] + , 1HNMR (δ, CDCl3): 8.32(1H,s); 8.19(1H,s); 8.06~8.02(2H,m); 7.83~7.81(1H,m); 7.73~7.65(5H,m ); 7.62~7.55(6H,m); 7.52~7.35(10H,m); 7.25~7.16(6H,m); 7.13~7.06(3H,m); 7.03~6.97(6H,m).

[0143] Example 2

[0144] The preparation of compound C125 comprises the following steps:

[0145] Step 1: Preparation of compound Int-4

[0146]

[0147] Under nitrogen protection, 22.0 mmol of Int-3' (reactant 1, prepared by the synthetic method of reference example 1), 20.0 mmol of diphenylamine (reactant 2), 30.0 mmol of sodium tert-butoxide and 60 mL of toluene were mixed, and then 0.1 mmol of Pd2(dba)3 catalyst and 0.2 mmol of Xantphos were added. The temperature was raised to 110°C and stirred for reaction for 15 hours. The mixture was cooled to room temperature, 50 mL of water was added, and the mixture was extracted with ethyl acetate. The organic phase was collected and dried, filtered, and the filtrate was concentrated and dried under reduced pressure. The compound Int-4 was separated and purified by silica gel column to obtain a white solid with a yield of 82%.

[0148] Step 2: Preparation of compound C125

[0149]

[0150] Under nitrogen protection, 20.0 mmol of Int-4, 22.0 mmol of diphenylamine (reactant 3), 30.0 mmol of sodium tert-butoxide and 60 mL of toluene were mixed, and then 0.1 mmol of Pd2(dba)3 catalyst and 0.2 mmol of 10% tri-tert-butylphosphonium toluene solution were added. The temperature was raised to 100°C and stirred for reaction for 15 hours. The mixture was cooled to room temperature, 50 mL of water was added, and the mixture was extracted with dichloromethane. The organic phase was collected and dried, filtered, and the filtrate was concentrated and dried under reduced pressure. The compound C125 was separated and purified by silica gel column to obtain a white solid with a yield of 87%. MS (TOF): m / z 808.3266 [M+H] + , 1HNMR(δ, CDCl3): 8.26(1H,s); 8.06~7.98(4H,m); 7.74~7.69(2H,m); 7.63~7.58(5H,m); 7.52~7.45(6H,m); 7 .41~7.35(4H,m); 7.26~7.20(5H,m); 7.11~7.03(7H,m); 6.98~6.93(4H,m); 6.89~6.87(2H,m); 6.85(1H,s).

[0151] The following compounds were prepared by similar synthetic methods as described above:

[0152]

[0153]

[0154]

[0155]

[0156]

[0157]

[0158]

[0159]

[0160]

[0161]

[0162]

[0163]

[0164] Example 3

[0165] The preparation of compound C191 comprises the following steps:

[0166] Step 1: Preparation of compound Int-5

[0167]

[0168] Referring to the synthesis method of Example 1, the o-iodobenzonitrile in the first step of Example 1 was replaced by methyl 2-iodo-3-naphthoate, and the THF solution of p-bromophenyllithium was replaced by the THF solution of m-chlorophenyllithium to obtain compound Int-5 with a yield of 82%.

[0169] Step 2: Preparation of compound Int-6

[0170]

[0171] Referring to the synthesis method of Example 1, only Int-1 in the second step of Example 1 was replaced by Int-5 to obtain compound Int-6 with a yield of 74%.

[0172] Step 3: Preparation of compound Int-7

[0173]

[0174] Referring to the synthesis method of Example 1, only Int-2 in the third step of Example 1 was replaced by Int-6 to obtain compound Int-7 with a yield of 52%.

[0175] Step 4: Preparation of compound Int-8

[0176]

[0177] Under nitrogen protection, 22.0 mmol of Int-7 prepared in the previous step (reactant 1), 20.0 mmol of biphenylaniline (reactant 2), 30.0 mmol of sodium tert-butoxide, 0.1 mmol of Pd2(dba)3, 0.2 mmol of Xantphos and 80 mL of toluene solution were mixed, the temperature was raised to 110°C and stirred for reaction for 15 hours, the temperature was cooled to room temperature, 50 mL of water was added, the organic phase was separated, the aqueous phase was extracted with dichloromethane, the organic phase was dried, filtered, the filtrate was concentrated and dried under reduced pressure, and separated and purified by silica gel column to obtain compound Int-8 with a yield of 84%.

[0178] Step 5: Preparation of compound C191

[0179]

[0180] Under nitrogen protection, 22.0mmol of Int-8 prepared in the previous step, 20.0mmol of diphenylamine (reactant 3), 30.0mmol of sodium tert-butoxide, 0.1mmol of Pd2(dba)3, 0.3mmol of 10% tri-tert-butylphosphine toluene solution and 60mL of toluene solution were mixed, heated to 100°C and stirred for reaction for 15 hours, cooled to room temperature, 50mL of water was added, the organic phase was separated, the aqueous phase was extracted with dichloromethane, the organic phase was dried, filtered, the filtrate was concentrated and dried under reduced pressure, and separated and purified by silica gel column to obtain compound C191 with a yield of 86%. The white solid had a yield of 85%. MS (TOF): m / z 782.3189 [M+H] + , 1HNMR (δ, CDCl3): 8.70(1H,s); 8.52(1H,s); 8.37(1H,s); 8.05~7.97(5H,m); 7.76~7.72(4H,m); 7.62~7.5 8(2H,m); 7.56~7.50(5H,m); 7.48~7.36(7H,m); 7.25~7.15(8H,m); 7.11~7.06(2H,m); 7.03~6.97(3H,m).

[0181] The following compounds were prepared by similar synthetic methods to those in the above examples:

[0182]

[0183]

[0184]

[0185] In the above embodiment, G is selected from O, S, CR 7 R 8 or NAr 3 ; Among them, R 7 and R 8 are methyl, phenyl or fluorenyl respectively;

[0186] Ar 3 Any of the following groups:

[0187]

[0188] Example 4

[0189] An OLED element 100, such as Figure 1 As shown, the OLED element of this embodiment is a top emission element, including a substrate 101, an anode 102 arranged on the substrate 101, a hole injection layer 103 arranged on the anode layer 102, a hole transport layer 104 arranged on the hole injection layer 103, an electron blocking layer 105 arranged on the hole transport layer 104, an organic light emitting layer 106 arranged on the electron blocking layer 105, a hole blocking layer 107 arranged on the organic light emitting layer 106, an electron transport layer 108 arranged on the hole blocking layer 107, an electron injection layer 109 arranged on the electron transport layer 108, a cathode 110 arranged on the electron injection layer 109, and a capping layer 111 on the cathode. The preparation method of the OLED element without the hole blocking layer 107 comprises the following steps:

[0190] 1) The glass substrate coated with the ITO conductive layer was ultrasonically treated in a cleaning agent for 30 minutes, rinsed in deionized water, ultrasonically treated in an acetone / ethanol mixed solvent for 30 minutes, baked in a clean environment until completely dry, irradiated with an ultraviolet cleaning machine for 10 minutes, and bombarded with a low-energy cation beam.

[0191] 2) Place the treated ITO glass substrate in a vacuum chamber and evacuate the chamber to a vacuum of less than 1×10 -5 Pa, and silver is evaporated on the above ITO film as the anode layer, and the thickness of the evaporated film is Continue to evaporate compounds HI01 and HI02 as hole injection layers, where HI02 is 3% of the mass of HI01 and the evaporated film thickness is

[0192] 3) Continue to evaporate the compound HTM on the hole injection layer to form a hole transport layer, and the evaporated film thickness is

[0193] 4) Compound HT025 was continuously evaporated on the hole transport layer as an electron blocking layer, and the thickness of the evaporated film was

[0194] 5) Compound RH01 is continuously evaporated on the electron blocking layer as the main material and RD030 is the doping material, wherein RD030 is 5% of the mass of RH01, as the organic light-emitting layer of the element, and the film thickness of the organic light-emitting layer obtained by evaporation is

[0195] 6) A layer of LiQ and compound ET036 is continuously evaporated on the organic light-emitting layer as the electron transport layer of the element, wherein the compound ET036 is 40% of the mass of LiQ and the evaporated film thickness is

[0196] 7) Continue to evaporate a layer of LiF on the electron transport layer as an electron injection layer, and the evaporated film thickness is

[0197] 8) On the electron injection layer, magnesium and silver are evaporated as the transparent cathode layer of the element. The mass ratio of magnesium to silver is 1:10, and the thickness of the evaporated film is

[0198] 9) A layer of the compound represented by formula (I) of the present invention is evaporated on the transparent cathode layer as the CPL layer of the element, and the evaporated film thickness is The OLED element provided by the present invention is obtained.

[0199] The structures of the compounds used in the above application examples are as follows:

[0200]

[0201]

[0202] An organic electroluminescent element 200, the structure of which is as follows Figure 2 As shown, it includes a substrate 201, an anode 202, a hole injection layer 203, a hole transport layer 204, a first light-emitting layer 205, an electron transport layer 206, a charge generation layer 207, a hole injection layer 208, a hole transport layer 209, a second light-emitting layer 210, an electron transport layer 211, an electron injection layer 212 and a cathode 213. The electroluminescent element 200 is prepared by a preparation method similar to that in Example 4.

[0203] Comparative Example 1

[0204] According to the same steps as in Example 4, the compound of formula (I) of the present invention in step 9) is replaced with E01 to obtain comparative element 1;

[0205]

[0206] At the same brightness, the driving voltage and current efficiency of the organic electroluminescent elements prepared in Example 4, Example 5 and Comparative Example 1, as well as the life of the element, were measured using a digital source meter and a brightness meter. Specifically, the voltage was increased at a rate of 0.1 V per second, and the current density of the organic electroluminescent element was measured to be 10 mA / cm 2 The ratio of brightness to current density is the current efficiency. All the results are summarized in Table 1.

[0207] Table 1 Performance test results of each component

[0208]

[0209]

[0210]

[0211]

[0212]

[0213] Among them, Me is methyl; Ph is phenyl; PhPh is biphenyl, Nap is naphthyl, and FR is 9,9-fluorenyl.

[0214] From the results in Table 1, it can be seen that after the compound of the present invention is used as a CPL material in an OLED light-emitting element, the light extraction is significantly improved compared with the comparative element 1, and the brightness and luminous efficiency of the element are improved under the same current density condition. Due to the improvement of brightness and efficiency, the power consumption of the element at the same brightness is reduced, and the life of the element is also improved. This shows that the compound of the present invention is an organic electroluminescent material with excellent performance.

[0215] The organic electroluminescent device of the present invention can be used in planar light emitters of wall-mounted televisions, flat-panel displays, lighting, etc., backlight sources of copiers, printers, liquid crystal displays, light sources of measuring instruments, etc., display panels, sign lights, etc.

[0216] The above is only a specific embodiment of the present invention, but the protection scope of the present invention is not limited thereto. Any person skilled in the art can easily think of changes or substitutions within the technical scope disclosed by the present invention, which should be included in the protection scope of the present invention. Therefore, the protection scope of the present invention should be based on the protection scope of the claims.

Claims

1. An amino compound, characterized in that The amino compound is selected from one or more of the following structures C01 to C204: Wherein, G is selected from O, S, CR 7 R 8 or NAr 3 ; The R 7 and R 8 are methyl, phenyl or fluorenyl respectively; The Ar 3 Selected from the group consisting of:

2. An organic electroluminescent material, characterized in that: The organic electroluminescent material comprises the amino compound according to claim 1.

3. An organic electroluminescent device, characterized in that: The organic electroluminescent device comprises a first electrode, a second electrode, a capping layer and at least one organic layer disposed between the first electrode and the second electrode, wherein the capping layer comprises the amino compound according to claim 1.

4. The organic electroluminescent device according to claim 3, characterized in that: The organic layer includes a hole injection layer, a hole transport layer, an electron blocking layer, a light emitting layer, a hole blocking layer, an electron transport layer, an electron injection layer or a charge generating layer; wherein each organic layer is one layer, two layers or multiple layers.

5. A consumer product, characterized in that: An organic electroluminescent device comprising any one of claims 3 to 4.

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