Patent Application
20230157161
Pursuant to 35 U.S.C. § 119(a), this application claims the benefit of the priority to Chinese Patent Application No. 202111367059.0, filed on Nov. 18, 2021. The content of the prior application is incorporated herein by its entirety.
The present invention belongs to the field of electroluminescence material, which relates to an organic material composition and applications thereof.
An electroluminescence (EL) device is a self-luminous display device which is advantageous for its wider angle of view, higher contrast ratio, and faster response time.
The most important key factor to decide the light-emitting efficiency of an EL device is the light-emitting material. A light-emitting material needs to have the following characteristics: high quantum efficiency, high mobility of electrons and holes, and the uniformity and stability of the light-emitting layer formed by the light-emitting material.
Recently, it is urgent to develop an organic EL device having higher light-emitting efficiency and longer service life. Specifically, in light of the EL characteristics needed for medium and large organic light-emitting diodes (OLED) panels, an excellent light-emitting material superior to regular materials is urgently needed. Thus, a high glass transition temperature and a high pyrolysis temperature are required for the host material in order to achieve high thermal stability and high electrochemical stability, thereby resulting in a longer service life, good formability of amorphous films, good adhesion with adjacent layers, and good immobility between layers.
To enhance color purity, light-emitting efficiency and stability, the light-emitting material as a host material can be used in a combination of a host material and a dopant. Generally, an EL device with good characteristics has an emitting layer structure formed by a material in which a dopant is doped into a host material. When the dopant/host material system is used as the light-emitting material, the host material will greatly influence the efficiency and service life of the EL device. Thus, the host material is important.
To overcome the shortcomings of the existing technology, the objective of the present invention is to provide an organic material composition and applications thereof.
To achieve the above objective, the present invention uses the following technical approaches:
In one aspect, the present invention provides an organic material composition comprising at least one compound having a structure represented by Formula (1) and at least one compound having a structure represented by Formula (2),
wherein, R is selected from hydrogen, deuterium, halogen, a cyano group, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted C3-C30 cycloalkyl group, a substituted or unsubstituted C6-C30 aryl group, and a substituted or unsubstituted C3-C30 heteroaryl group;
R1 is -L1Ar1; R2 is -L2Ar2; R3 is -L3Ar3; R4 is -L4Ar4;
L1 to L4 are each independently selected from a bond, a substituted or unsubstituted C6-C30 arylene group, and a substituted or unsubstituted C3-C30 heteroarylene group;
Ar1 to Ar4 are each independently selected from hydrogen, deuterium, halogen, a cyano group, a substituted or unsubstituted C6-C60 aryl group, and a substituted or unsubstituted C3-C60 heteroaryl group;
wherein, R′ is selected from hydrogen, deuterium, halogen, a cyano group, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted C3-C30 cycloalkyl group, a substituted or unsubstituted C6-C30 aryl group, and a substituted or unsubstituted C3-C30 heteroaryl group;
L5 to L8 are each independently selected from a bond, a substituted or unsubstituted C6-C30 arylene group, and a substituted or unsubstituted C3-C30 heteroarylene group;
Ar5 to Ar8 are each independently selected from hydrogen, deuterium, halogen, a cyano group, a substituted or unsubstituted C6-C60 aryl group, and a substituted or unsubstituted C3-C60 heteroaryl group.
In the present invention, by the combination of at least one compound having a structure represented by Formula (1) and at least one compound having a structure represented by Formula (2), the organic material composition not only has an energy level that can be aligned with the energy levels of the adjacent layers, but also has a higher triplet energy level, which are advantageous for the recombination of charge carriers in the emitting layer, thereby increasing light-emitting efficiency.
Preferably, in Formula (1), at least one of Ar1 to Ar4 is a group represented by Formula (a):
wherein the wavy line represents the connection position of the group;
X1 is selected from N and CRX1; X2 is selected from N and CRX2; X3 is selected from N and CRX3; X4 is selected from N and CRX4; X5 is selected from N and CRX5;
RX1 to RX5 are each independently selected from hydrogen, deuterium, halogen, a cyano group, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted C3-C30 cycloalkyl group, a substituted or unsubstituted C6-C30 aryl group, and a substituted or unsubstituted C3-C30 heteroaryl group; RX1 to RX5 are present individually without forming a ring, or any adjacent two of RX1 to RX5 joined to form a ring, and the ring is a benzene ring.
Preferably, X1 is N; X2 is N; X3 is CRX3; X4 is CRX4; X5 is CRX5.
Preferably, X1 is N; X3 is N; X2 is CRX2; X4 is CRX4; X5 is CRX5.
Preferably, X1 is N; X2 is N; X3 is N; X4 is CRX4; X5 is CRX5.
Preferably, the Formula (a) is selected from
and RX5 is the same as described above.
Preferably, the Formula (a) is selected from
and RX2 is the same as described above.
Preferably, in Formula (1), the RX1 to RX5 are each independently selected from hydrogen, deuterium, halogen, and a group selected from a phenyl group, a biphenylyl group, a terphenylyl group, a naphthyl group, a phenanthryl group, an anthryl group, a phenylnaphthyl group, a naphthylphenyl group, a pyridyl group, a bipyridyl group, a dibenzofuryl group, a dibenzothiophenyl group, a carbazolyl group, a carbazolylphenyl group, a phenylcarbazolyl group, a dimethylfluorenyl group, a diphenylfluorenyl group, a spiro-bifluorenyl group, a dibenzofurylphenyl group, a dibenzothiophenylphenyl group, a dimethylfluorenylphenyl group, a benzocarbazolyl group, a benzonaphthofuryl group, and a benzonaphthothiophenyl group, each of which is substituted or unsubstituted.
Preferably, in Formula (1), at least one of the R1, R2, R3 and R4 is hydrogen.
Preferably, at least two of the R1, R2, R3 and R4 are hydrogen.
Preferably, at least three of the R1, R2, R3 and R4 are hydrogen.
Preferably, the R2 is -L2Ar2; and R1, R3, and R4 are all hydrogen.
Preferably, the R3 is -L3Ar3; and R1, R2, and R4 are all hydrogen.
Preferably, the R is selected from a phenyl group and a biphenylyl group, each of which is substituted or unsubstituted.
Preferably, the R′ is selected from a phenyl group and a biphenylyl group, each of which is substituted or unsubstituted.
Preferably, L1 to L4 are each independently selected from a bond, a substituted or unsubstituted phenylene group, a substituted or unsubstituted naphthylene group, and a substituted or unsubstituted biphenylene group.
In the present invention, the compound having a structure represented by Formula (1) is a compound having electron transport properties.
Preferably, the compound having a structure represented by Formula (1) is any one of the following compounds M1 to M206:
wherein D represents deuterium.
Preferably, at least one of Ar5 to Ar8 is
wherein Ar9 and Ar10 are each independently selected from a substituted or unsubstituted C6-C30 aryl group, and a substituted or unsubstituted C3-C30 heteroaryl group.
Preferably, Ar9 and Ar10 are each independently selected from a phenyl group, a biphenylyl group, a terphenylyl group, a naphthyl group, a phenanthryl group, an anthryl group, a triphenylenylene group, a phenylnaphthyl group, a naphthylphenyl group, a pyridyl group, a bipyridyl group, a dibenzofuryl group, a dibenzothiophenyl group, a benzonaphthofuryl group, a benzonaphthothiophenyl group, a dinaphthofuryl group, a dinaphthothiophenyl group, a dibenzofurylphenyl group, a dibenzothiophenylphenyl group, a phenylcarbazolyl group, a dimethylfluorenyl group, a benzodimethylfluorenyl group, a diphenylfluorenyl group, a spiro-bifluorenyl group, and a dimethylfluorenylphenyl group, each of which is substituted or unsubstituted.
Preferably, Ar5 is
Preferably, Ar6 is
Preferably, Ar7 is
Preferably, Ar8 is
In the present invention, the compound having a structure represented by Formula (2) is a compound having hole transport properties.
Preferably, the compound having a structure represented by Formula (2) is any one of the following compounds N1 to N60:
Preferably, the compound having a structure represented by Formula (1) and the compound having a structure represented by Formula (2) have a weight ratio of 1:9 to 9:1, such as 1:9, 2:8, 3:7, 4:6, 5:5, 6:4, 7:3, 8:2, 9:1, or the like; preferably 2:8 to 8:2; more preferably 3:7 to 7:3; even more preferably 4:6 to 6:4.
In the present invention, with the limitation of the group is substituted or unsubstituted, when the group is substituted, the substituent is selected from deuterium, halogen, a cyano group, a nitro group, an unsubstituted or R″-substituted C1-C4 straight or branched alkyl group, an unsubstituted or R″-substituted C6-C20 aryl group, an unsubstituted or R″-substituted C3-C20 heteroaryl group, and an unsubstituted or R″-substituted C6-C20 arylamino group; R″ is selected from deuterium, halogen, a cyano group and a nitro group.
Preferably, the aryl group is selected from a phenyl group, a biphenylyl group, a terphenylyl group, a naphthyl group, an anthryl group, a phenanthryl group, a benzophenanthryl group, a naphthylphenyl group, a dimethylfluorenyl group, a diphenylfluorenyl group and a spiro-bifluorenyl group.
Preferably, the heteroaryl group is selected from a pyridyl group, a dibenzofuryl group, a dibenzothiophenyl group, a carbazolyl group, a phenylcarbazolyl group, a pyridylcarbazolyl group, a naphthylcarbazolyl group, a biphenylylcarbazolyl group, a dibenzofurylphenyl group, a dibenzothiophenylphenyl group, a benzonaphthofuryl group, a benzonaphthothiophenyl group, a benzocarbazolyl group and a dibenzocarbazolyl group.
Preferably, the alkyl group is selected from a methyl group, an ethyl group, a propyl group, a tert-butyl group, a cyclohexyl group and adamantyl.
As used in the present invention, the term “halogen” may comprise fluorine, chlorine, bromine or iodine.
As used in the present invention, the term “C1-C30 alkyl group” indicates a monovalent substituent derived from a straight or branched saturated hydrocarbon having 1 to 30 carbon atoms, for example, it comprises, but is not limited to, a methyl group, an ethyl group, a propyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an isopentyl group, or a hexyl.
As used in the present invention, the term “C3-C30 cycloalkyl group” indicates a group derived from a monocyclic hydrocarbon or a multicyclic hydrocarbon having 1 to 30 carbon atoms on the main chain, and the cycloalkyl group may comprise cyclopropyl, cyclobutyl, adamantyl group, or the like.
In the present invention, the aryl group and arylene group comprise a monocyclic, a multicyclic or a fused cyclic aryl group, in which the rings may be interrupted by a short non-aromatic unit, and they may comprise a spiro-structure. The aryl group and arylene group of the present invention comprise, but are not limited to, a phenyl group, a biphenylyl group, a terphenylyl group, a naphthyl group, a phenanthryl group, an anthryl group, a fluorenyl group, a spiro-bifluorenyl group, or the like.
In the present invention, the heteroaryl group and heteroarylene group comprise a monocyclic, a multicyclic or a fused cyclic heteroaryl group, in which the rings may be interrupted by a short non-aromatic unit, and the hetero atom comprises nitrogen, oxygen or sulfur. The heteroaryl group and heteroarylene group of the present invention comprise, but are not limited to, a furyl group, a thiophenyl group, a pyrrolyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, a thiadiazolyl group, an isothiazolyl group, an isoxazolyl group, an oxazolyl group, an oxadizolyl group, a triazinyl group, a tetrazinyl group, a triazolyl group, a tetrazolyl group, a furazanyl group, a pyridyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a benzofuryl group, a benzothiophenyl group, an isobenzofuryl group, a dibenzofuryl group, a dibenzothiophenyl group, a benzimidazolyl group, a benzothiazolyl group, a benzisothiazolyl group, a benzisoxazolyl group, a benzoxazolyl group, an isoindolyl group, an indolyl group, an indazolyl group, a benzothiadiazolyl group, a quinolyl group, an isoquinolyl group, a cinnolinyl group, a quinazolinyl group, a quinoxalinyl group, a carbazolyl group, a phenoxazinyl group, a phenothiazinyl group, a phenanthridinyl group, a 1,3-benzodioxolyl group, a dihydroacridinyl group, or derivatives thereof.
Preferably, the aryl group is selected from a phenyl group, a biphenylyl group, a terphenylyl group, a naphthyl group, an anthryl group, a phenanthryl group, a 9,9′-dimethylfluorenyl group, a 9,9′-diphenylfluorenyl group and a spiro-bifluorenyl group.
Preferably, the heteroaryl group is selected from a dibenzofuryl group, a dibenzothiophenyl group, a carbazolyl group, a triazinyl group, a pyridyl group, a pyrimidinyl group, an imidazolyl group, an oxazolyl group, a thiazolyl group, a benzimidazolyl group, a benzoxazolyl group, a benzothiazolyl, a naphthimidazolyl group, a naphthoxazolyl group, a naphthothiazolyl group, a phenanthrimidazolyl group, a phenanthroxazolyl group, a phenanthrothiazolyl group, a quinoxalinyl group, a quinazolinyl group, an indolocarbazolyl group, an indolofluorenyl group, a benzothienopyrazinyl group, a benzothienopyrimidinyl group, a benzofuropyrazinyl group, a benzofuropyrimidinyl group, an indolopyrazinyl group, an indolopyrimidinyl group, an indenopyrazinyl group, an indenopyrimidinyl group, a spiro[fluorene-9,1′-indene]-pyrazinyl group, spiro[fluorene-9,1′-indene]-pyrimidinyl group, benzofurocarbazolyl and benzothienocarbazolyl.
As used in the present invention, the term “C6-C30 aryloxy group” indicates a monovalent substituent represented by ZO—, wherein Z represents an aryl group having 6 to 30 carbon atoms. Examples of such aryloxy group comprise, but are not limited to, a phenoxy group, a naphthyloxy group, a diphenoxy group, or the like.
As used in the present invention, the term “C1-C30 alkoxy group” indicates a monovalent substituent represented by Z′O—, wherein Z′ represents an alkyl group having 1 to 30 carbon atoms.
As used in the present invention, the term “substituted” indicates a hydrogen atom comprised in a compound is replaced by another substituent. The position of substitution is not specifically limited, provided that the hydrogen at the position can be replaced by the substituent. When two or more substituents are simultaneously present, the two or more substituents can be the same or different.
As used in the present invention, unless otherwise specified, the hydrogen atom comprises protium, deuterium or tritium.
In the present invention, “adjacent two groups joined to form a ring” indicates that 2 substituents at adjacent positions on the same ring or adjacent rings can be joined to form a ring by chemical bonding. The specific way to form a ring in the present invention is not limited (for example, joined via a single bond, joined via a benzene ring, joined via a naphthalene ring, fused via
fused via
fused via
fused via
fused via
wherein the represents fusion positions). In the same description present hereinafter, it has the same meaning.
In the present invention, when the range of carbon atom number is limited in the definition of a functional group, the functional group may have a carbon atom number of any integer in the limited range. For example, a C6-C60 aryl group represents an aryl group that may give a carbon number of any one integer comprised in the range of 6 to 60, such as 6, 8, 10, 15, 20, 30, 35, 40, 45, 50, 55 or 60, etc.
In the present invention, the organic compounds substituted at each of the described positions are prepared by a synthesis route shown as below:
R5″ is chlorine; R5′ is
X is halogen, preferably chlorine or bromine.
R6″ is chlorine; R6′ is
X is halogen, preferably chlorine or bromine.
R7″ is chlorine; R7′ is
X is halogen, preferably chlorine or bromine.
R8″ is chlorine; R8′ is
X is halogen, preferably chlorine or bromine.
Buchwald-Hartwig synthesis method is mainly used to synthesize Formula (2).
In another aspect, the present invention provides an organic electroluminescence material, and the organic electroluminescence material comprises the above-mentioned organic material composition.
In another aspect, the present invention provides an application of the above-mentioned organic material composition or the above-mentioned organic electroluminescence material in preparation of an optical element.
Preferably, the optical element comprises any one of an organic electroluminescence element, an organic field-effect transistor, an organic thin film transistor, an organic light-emitting transistor, an organic integrated circuit, an organic solar cell, an organic field quenching element, a light-emitting electrochemical cell, an organic laser diode, and an organic photoreceptor.
In another aspect, the present invention provides an organic electroluminescence element, wherein the organic electroluminescence element comprises an anode, a cathode, and an organic layer disposed between the anode and the cathode, and the organic layer comprises the above-mentioned organic material composition or the above-mentioned organic electroluminescence material.
Preferably, the organic layers comprise a hole injection layer, a hole transport layer, an emitting layer, an electron transport layer and an electron injection layer, which are sequentially layered from a side of the anode to a side of the cathode.
Preferably, the emitting layer is made of a material comprising a host material and a guest material, wherein the host material comprises the above-mentioned organic material composition or the above-mentioned organic electroluminescence material.
Preferably, the guest material comprises a phosphorescence dopant, and the phosphorescence dopant comprises a coordination complex of a transition metal.
In another aspect, the present invention provides an organic electroluminescence device, wherein the organic electroluminescence device comprises the above-mentioned organic electroluminescence element.
Compared to the existing technology, the present invention has the following advantages:
By the combination of at least one compound having a structure represented by Formula (1) and at least one compound having a structure represented by Formula (2), the organic material composition of the present invention makes an organic light-emitting element have an obviously enhanced light-emitting efficiency.
Specific embodiments are further illustrated by the following examples to demonstrate the technical approaches of the present invention. Those skilled in the art should understand that the illustrative examples are helpful to understand the present invention; however, they should not be construed as being limiting to the scope of the present invention.
The compounds whose synthesis methods are not mentioned in the present invention are commercially available products used as raw materials. The solvents and agents used in the present invention, for example, chemical agents such as tetrahydrofuran, potassium hydroxide, nitrobenzene, palladium catalyst and the like, can be purchased in the chemical product market in China, for example, purchased from Sinopharm Chemical Reagent Co., Ltd.; Tokyo Chemical Industry (TCI) Co., Ltd.; Bide Pharmatech Ltd.; J&K Scientific Ltd. and the like. In addition, these compounds can also be synthesized with a well-known method by those skilled in the art.
Synthesis of M6-B: In a three-necked bottle of 25 milliliters (mL), M6-A (10 millimoles (mmol)), nitrobenzene (10 mmol), potassium hydroxide (22 mmol), copper(I) thiocyanate (1 mmol) and anhydrous tetrahydrofuran (10 mL) were added, nitrogen gas was purged for three times, and heated to 90° C. under nitrogen gas protection to react for 48 hours (h). After the reaction ended, the reaction mixture was quenched by water, the reaction system was extracted by ethyl acetate, and the organic solvent was removed by rotary evaporation to give a crude product. The crude product was purified by column chromatography (ethyl acetate:n-hexane=1:50 (volume ratio)), to obtain M6-B (1.34 g, 49% yield).
Synthesis of M6-B′: In a three-necked bottle of 50 mL, 2-bromo chlorobenzaldehyde (10 mmol), bis(pinacolato)diboron (12 mmol), potassium acetate (100 mmol), [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloride (0.2 mmol) and 1,4-dioxane (25 mL) were added, nitrogen gas was purged, and heated to 100° C. under nitrogen gas protection for reaction. After the reaction ended, the reaction mixture was quenched by water, extracted by methylene dichloride to give a crude product. The crude product was purified by column chromatography (methylene dichloride:n-hexane=1:50 (volume ratio)), to obtain M6-B′ (1.7 g, 64% yield).
Synthesis of M6-C: In a three-necked bottle of 50 mL, M6-B (10 mmol), M6-B′ (10 mmol), sodium bicarbonate (20 mmol), tetrakis(triphenylphosphine)palladium (0.2 mmol), tetrahydrofuran (20 mL) and water (10 mL) were added, nitrogen gas was purged, and heated to 60° C. under nitrogen gas protection to react overnight. After the reaction ended, the reaction mixture was quenched by water, extracted by methylene dichloride, and the organic solvent was removed by rotary evaporation to give a crude product. The crude product was purified by column chromatography (ethyl acetate:n-hexane=1:50 (volume ratio)), to obtain M6-C (3.06 g, 92% yield).
Synthesis of M6-D: In a three-necked bottle of 50 mL, M6-C (10 mmol), (methoxymethyl)triphenylphosphonium chloride (20 mmol) and tetrahydrofuran (10 mL) were added, and the temperature was reduced to 0° C. Potassium tert-butoxide (2 mmol) was resolved in 5 mL tetrahydrofuran. The three-necked bottle was purged with nitrogen gas. Under nitrogen gas protection, the potassium tert-butoxide solution was added dropwise at 0° C. to obtain a mixture. After the addition, the mixture was stirred to react for half an hour. After the reaction ended, the reaction mixture was quenched by water, extracted by methylene dichloride, and the organic solvent was removed by rotary evaporation to give a crude product. The crude product was purified by column chromatography (ethyl acetate:n-hexane=1:50 (volume ratio)), to obtain M6-D (1.8 g, 50% yield).
Synthesis of M6-E: In a three-necked bottle of 25 mL, M6-D (1 mmol) and hexafluoroisopropanol (5 mL) were added, the temperature was reduced to 0° C., and nitrogen gas was purged. Under nitrogen gas protection, trifluoromethanesulfonic acid (1 mL) was added dropwise to obtain a mixture, and the mixture was stirred to react for half an hour to give a crude product. The crude product was purified by column chromatography (ethyl acetate:n-hexane=1:50 (volume ratio)), to obtain M6-E (0.24 g, 73% yield).
Synthesis of M6-F: In a three-necked round-bottom flask of 50 mL, M6-E (10 mmol), bis(pinacolato)diboron (12 mmol), sodium acetate (20 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.5 mmol) and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (1.5 mmol) were added, then 1,4-dioxane (20 mL) was added, nitrogen gas was purged for three times, and heated to 100° C. under nitrogen gas protection for reaction. After the reaction ended, the reaction mixture was quenched by water, extracted by methylene dichloride, and the organic solvent was removed by rotary evaporation to give a crude product. The crude product was purified by column chromatography (ethyl acetate:n-hexane=1:50 (volume ratio)), to obtain M6-F (3.24 g, 77% yield).
Synthesis of M6: In a three-necked round-bottom flask of 100 mL, a stir bar was put at the bottom and a refluxing tube was connected on the top. The flask was dried and purged with nitrogen gas, and M6-F (10 mmol), M6-G (10 mmol, CAS1689576-03-1), sodium bicarbonate (23 mmol), tetrakis(triphenylphosphine)palladium (0.5 mmol), bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (0.5 mmol), toluene (25 mL), ethanol (7 mL) and water (7 mL) were separately added, nitrogen gas was purged for three times, and heated to 80° C. under nitrogen gas protection to react for 8 h. After the reaction ended, the reaction mixture was extracted by ethyl acetate, and the resulting extract was dried by magnesium sulfate, filtered, and dried by rotary evaporation to give a crude product. The crude product was purified by column chromatography (ethyl acetate:n-hexane=1:10 (volume ratio)), to obtain compound M6 (4.13 g, 67% yield).
Anal. Calcd. C41H26N6: C, 81.71; H, 4.35; N, 13.94. Found: C, 81.78; H, 4.33; N, 13.89. HRMS (ESI) m/z [M+H]+: Calcd.: 602.22. Found: 603.40.
Synthesis of M160-B″: Similar to the synthesis of M6-B′, with the difference that 2-bromo-5-chlorobenzaldehyde is used to replace 2-bromo chlorobenzaldehyde, to obtain M160-B″ (1.60 g, 60% yield).
Synthesis of M160-C: Similar to the synthesis of M6-C, with the difference that 4-fluoro-2-formylbenzeneboronic acid pinacol ester is used to replace 5-fluoro-2-formylbenzeneboronic acid pinacol ester, to obtain M160-C (2.13 g, 64% yield).
Synthesis of M160-D: Similar to the synthesis of M6-D, with the difference that M160-C is used to replace M6-C, to obtain M160-D (3.21 g, 89% yield).
Synthesis of M160-E: Similar to the synthesis of M6-E, with the difference that M160-D is used to replace M6-D, to obtain M160-E (0.16 g, 48% yield).
Synthesis of M160-F: Similar to the synthesis of M6-F, with the difference that M160-E is used to replace M6-E, to obtain M160-F (4.00 g, 95% yield).
Synthesis of compound M160: Similar to the synthesis of compound M6, with the difference that M160-F is used to replace M6-F, and M160-G is used to replace M6-G, to obtain compound M160 (4.70 g, 78% yield).
Anal. Calcd. C41H26N6: C, 81.71; H, 4.35; N, 13.94. Found: C, 81.73; H, 4.37; N, 13.90. HRMS (ESI) m/z (M+): Calcd.: 602.22. Found: 603.29.
The corresponding products shown in Table 1 were prepared by the above-mentioned preparation method using the Material 1 and Material 2 as raw materials. The structure and characteristic data of the products are shown in Table 2.
Synthesis of compound N4: In a three-necked bottle of 25 mL, nitrogen gas was purged, N4-A (1 mmol, CAS 2085325-19-3), N4-B (1 mmol, CAS 102113-98-4), sodium tert-butoxide (2 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.02 mmol), 50% tri-tert-butylphosphine solution (0.1 mmol) and toluene 8 mL was added, and stirred under reflux to react. After the reaction ended, the reaction mixture was cooled to room temperature, and the organic layer was extracted by ethyl acetate and H2O. The extracted organic layer was dried by MgSO4, filtered, and the filtrate was concentrated under vacuum to give a crude product. The crude product was purified by column chromatography (ethyl acetate:n-hexane=1:50 (volume ratio)), to obtain compound N4 (0.43 g, 69% yield).
Anal. Calcd. C45H30N2O: C, 87.92; H, 4.92; N, 4.56. Found: C, 87.97; H, 4.90; N, 4.53. FIRMS (ESI) m/z [M+H]+: Calcd.: 614.24. Found: 615.33.
Synthesis of N33: In a two-necked round-bottom flask of 25 mL, a stir bar was put at the bottom and a refluxing tube was connected on the top. The flask was dried and purged with nitrogen gas, and N33-A (1 mmol), N33-B (1 mmol, CAS 2468159-90-0), potassium carbonate (1.3 mmol), tetrakis(triphenylphosphine)palladium (0.05 mmol), toluene (7 mL), and water (2 mL) were separately added, nitrogen gas was purged for three times, and heated to 85° C. under nitrogen gas protection to react for 10 h. After the reaction ended, the reaction mixture was extracted by ethyl acetate, and the resulting extract was dried by magnesium sulfate, filtered, and dried by rotary evaporation to give a crude product. The crude product was purified by column chromatography (ethyl acetate:n-hexane=1:10 (volume ratio)), to obtain compound N33 (0.44 g, 63% yield).
Anal. Calcd. C45H28N2O2: C, 85.97; H, 4.49; N, 4.46. Found: C, 85.88; H, 4.52; N, 4.48. HRMS (ESI) m/z (M+): Calcd.: 628.22 Found: 629.10.
Compounds in Table 3 were synthesized by the same synthesis method for preparing compound N33. The raw materials and resulting products are shown in Table 3. The structure and characteristic data of the products are shown in Table 4.
An organic electroluminescence element (such as OLED) with the following layer structure was provided: base (indium tin oxide (ITO, as an anode) coated glass substrate)/hole injection layer (HIL)/hole transport layer (HTL)/emitting layer (EML)/electron transport layer (ETL)/electron injection layer (EIL), and the cathode at last.
The materials needed to prepare OLED are listed below, wherein the REF-1 is comparative compound 1:
The above-mentioned organic electroluminescence elements were prepared by the following steps:
(1) Cleaning the substrate: a glass substrate coated with transparent ITO layer (the anode) was ultrasonicated in an aqueous detergent (the content and concentration of the aqueous detergent: an ethylene glycol solvent of ≤10 percent by weight (wt %), triethanolamine of ≤1 wt %), washed in deionized water, degreased in an acetone/ethanol mixed solvent (volume ratio=1:1) by ultrasonication, baked in a clear environment until water was completely removed, and washed by ozone under ultraviolet light;
(2) Depositing organic emitting functional layers:
The glass substrate with the anode was placed in a chamber, and the chamber was vacuumized until 1×10−6 Pascal (Pa) to 2×10−4 Pa, and a mixture of HAT(CN)6 and HT (mass ratio of HAT(CN)6 and HT is 3:97) was deposited on the anode layer in vacuum to form a hole injection layer, in which the deposited thickness was 10 nanometers (nm).
A hole transport layer was deposited on the hole injection layer, in which the deposited thickness was 80 nm.
An emitting layer was deposited on the hole transport layer. Specifically, the preparation method was: the light-emitting host material and a guest material were co-deposited in vacuum, in which the total deposited thickness was 30 nm.
An electron transport layer was deposited on the emitting layer. Specifically, the preparation method was: BPhen and LiQ were co-deposited in vacuum, in which the total deposited thickness was 30 nm.
An electron injection layer was deposited on the electron transport layer, in which the total deposited thickness was 1 nm.
Al (as cathode) was deposited on the electron injection layer 6, in which the deposited thickness was 80 nm.
The materials (mat.) of each layer in the element and parameters such as thickness (thk.) of Element Examples 1 to 11 (E1 to E11) and Comparative Element Examples 1 to 2 (CE1 to CE2) are shown in Table 5.
Characteristic Tests of Elements:
Instruments: the characteristics such as current, voltage, luminance, emission spectrum and the like of the elements of the above Element Examples 1 to 11 and Comparative Element Examples 1 to 2 were synchronously tested by PR 650 SpectraScan Colorimeter and Keithley K 2400 SourceMeter;
Conditions for testing electrooptical characteristics: a current density of 10 milliamperes/square centimeter (mA/cm2) under room temperature;
Service life test: tested with a current density of 20 mA/cm2 under room temperature, and the time period recorded when the luminance of the tested element was reduced to 98% of the original luminance (in hour).
The test results of the elements are shown in Table 6.
From Table 6, it is clear that the organic material composition of the present invention obviously increases the current efficiency. When the organic material composition is used as the material of an organic functional layer, the element has a lower driving voltage (3.96 voltages (V) or lower), a higher current efficiency (20 Candelas/Ampere (Cd/A) or more) and a longer service life (218 h or more).
The applicant claims herein that even though the organic material composition of the present invention and the applications thereof are demonstrated by the above examples, the scope of the present invention is not limited by these examples. That is to say, it does not mean that the present invention has to be carried out based on the above examples. Those skilled in the art should understand that any improvement of the present invention, equivalent replacement of materials, addition of auxiliary components, selection of specific means and the like are all within the scope of protection and disclosure of the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202111367059.0 | Nov 2021 | CN | national |
