阅读说明：本技术 有机电致发光元件 (Organic electroluminescent element ) 是由 孙霞 谢再锋 蒋建兴 孙杰 于 2020-06-09 设计创作，主要内容包括：本发明提供一种有机电致发光元件。该有机电致发光元件包括由阳极至阴极依次设置的空穴传输区域、发光层及电子传输区域,空穴传输区域含有通式(1)的化合物,电子传输区域含有通式(2)的化合物,R-(1)至R-(8)相同或不同,且为氢、氘、C1-C4的烷基、C6-C30的芳基,或任选地与相邻基团结合成环；Ar-(1)和Ar-(2)相同或不同,且为C6-C30的芳基,L-(1)至L-(3)相同或不同,且为直接键或C6-C18的亚芳基；通式(2)中,Py为未取代的吡啶基；R-(9)选自氢、C1-C4的烷基或C6-C18的芳基；Ar-(3)选自C6-C18的芳基或杂芳基；L-(4)选自直接键或未取代的亚苯基；Z-(1)至Z-(3)中至少一个为N,其它为CH,驱动电压更低。(The invention provides an organic electroluminescent element. The organic electroluminescent element comprises a hole transport region, a light-emitting layer and an electron transport region arranged in this order from an anode to a cathode, wherein the hole transport region contains a compound represented by general formula (1), the electron transport region contains a compound represented by general formula (2), R 1 To R 8 Identical or different and are hydrogen, deuterium, alkyl of C1-C4, aryl of C6-C30, or optionally combine with adjacent groups to form a ring; ar (Ar) 1 And Ar 2 Identical or different and are a C6-C30 aryl radical, L 1 To L 3 Identical or different and is a direct bond or an arylene group of C6 to C18; in the general formula (2), Py is an unsubstituted pyridyl group; r 9 Selected from hydrogen, C1-C4 alkyl or C6-C18 aryl; ar (Ar) 3 Aryl or heteroaryl selected from C6-C18; l is 4 Selected from a direct bond or unsubstituted phenylene; z 1 To Z 3 At least one of them is N, the others are CH, and the driving voltage is lower.)

1. An organic electroluminescent element comprising a hole transporting region, a light-emitting layer and an electron transporting region arranged in this order from an anode to a cathode, wherein the hole transporting region contains a compound represented by general formula (1), and the electron transporting region contains a compound represented by general formula (2):

in the general formula (1) above,

R₁to R₈Are the same or different from each other and are each independently hydrogen, deuterium, a substituted or unsubstituted alkyl group of C1-C4, an aryl group of C6-C30, or optionally combine with adjacent groups to form a substituted or unsubstituted ring;

Ar₁and Ar₂Identical to or different from each other and each independently is a substituted or unsubstituted aryl group of C6-C30,

L₁to L₃Are the same or different from each other and are each independently a direct bond, or a substituted or unsubstituted arylene group of C6-C18;

in the general formula (2) in which,

py is unsubstituted pyridyl;

R₉selected from hydrogen, C1-C4 alkyl or substituted or unsubstituted C6-C18 aryl;

Ar₃aryl or heteroaryl selected from substituted or unsubstituted C6-C18;

L₄selected from a direct bond or unsubstituted phenylene;

Z₁to Z₃At least one of them is N, and the others are CH.

2. The organic electroluminescent element according to claim 1, wherein the compound represented by the general formula (1) is represented by any one of the following general formulae (1-a), (1-B), and (1-C):

in the general formulae (1-A), (1-B) and (1-C), R₁To R₈、Ar₁And Ar₂、L₁To L₃The same as defined in said general formula (1);

preferably, in the compounds represented by the general formulae (1-A), (1-B) and (1-C), R₁To R₈Are both H, L3 is a direct bond, L1 and L2 are direct bonds, Ar₁And Ar₂Is unsubstituted aryl of C6-C25;

preferably, the unsubstituted aryl group of C6-C25 is biphenyl, terphenyl, naphthalene, or anthracene;

more preferably, the biphenyl is ortho-biphenyl, meta-biphenyl, or para-biphenyl.

3. The organic electroluminescent element according to claim 1, wherein R in the compound represented by the general formula (1)₁To R₈Are both H, L3 is a direct bond, L1 and L2 are direct bonds, Ar₁And Ar₂Is unsubstituted aryl of C6-C25;

preferably, the unsubstituted aryl group of C6-C25 is biphenyl, terphenyl, naphthalene, or anthracene;

more preferably, the biphenyl is ortho-biphenyl, meta-biphenyl, or para-biphenyl.

4. The organic electroluminescent element according to claim 1, wherein the compound represented by the general formula (1) is selected from any one of the following compounds:

5. the organic electroluminescent element according to claim 1, wherein Py in the nitrogen-containing heterocyclic compound represented by the general formula (2) is a pyridyl group, R is a phenyl group, Ar is a phenyl group₃Is phenyl or naphthyl, L is phenylene;

preferably, the compound represented by the general formula (2) is selected from any one of the following:

6. the organic electroluminescent element according to claim 1, wherein the hole transport region comprises any one of a hole injection layer, a hole transport layer, a buffer layer, and an electron blocking layer; or the hole transport region includes any of a hole injection layer, a hole transport layer, a buffer layer, and an electron blocking layer, which are sequentially provided from the anode to the cathode, wherein at least one of the layers contains the compound represented by the general formula (1).

7. The organic electroluminescent element according to claim 1, wherein the electron transport region comprises any one of an electron injection layer, an electron transport layer, a buffer layer, and a hole blocking layer; or the electron transport region includes any of a hole blocking layer, a buffer layer, an electron transport layer, and an electron injection layer, which are sequentially provided from the anode to the cathode, and at least one of the layers contains the compound represented by the general formula (2).

8. The organic electroluminescent element according to any one of claims 1 to 7, wherein the light-emitting layer is composed of at least a host matrix and a guest dopant blend.

9. The organic electroluminescent element according to claim 8, wherein the host matrix is an anthracene compound represented by a general formula (3),

wherein R is₁₁And R₁₂Are the same or different from each other and are each independently hydrogen, substituted or unsubstituted alkyl of C1-C6, alkoxy, aryl or heteroaryl of C6-C30;

Ar₄、Ar₅each independently is selected from phenyl, biphenyl, naphthyl, anthryl, phenanthryl, naphthacenyl or pyrenyl;

a. b, c are each an integer of 1 to 4, and when a, b, c are each an integer of 2 or more, two or more structures in parentheses are the same as or different from each other.

10. The organic electroluminescent element according to claim 8, wherein the guest dopant of the light-emitting layer is a fluorescent dye represented by general formula (4),

wherein Ar is₆And Ar₇Are identical or different from one another and are each independently substituted or unsubstituted silyl, aryl or heteroaryl of C6-C30, or form a substituted or unsubstituted ring with one another;

Ar₈is substituted or unsubstitutedBenzofluorenyl, fluoranthenyl, pyrenyl orA group;

L₅is a direct bond, a substituted or unsubstituted arylene or heteroarylene group of C6-C18;

n is an integer of 1 to 4, and when n is an integer of 2 or more, two or more structures in parentheses are the same as or different from each other.

Technical Field

The present invention relates to an organic electroluminescent element. And more particularly, to an organic electroluminescent element.

Background

The organic electroluminescent device has been currently applied to the fields of smart phones, tablet computers, vehicles and the like, and is expanded in large-size application fields such as forward televisions and the like due to the characteristics of lightness, thinness, wide viewing angle, high contrast, low power consumption, high response speed, full-color pictures, flexibility and the like.

The organic electroluminescent element generally comprises a hole injection layer, a hole transport layer, an electron blocking layer, a luminescent layer, a hole blocking layer, an electron transport layer, an electron injection layer and other film layers, wherein holes and electrons are respectively injected from an anode and a cathode and enter the luminescent layer through the transport layer to be recombined and luminescent, the efficiency of the element depends on the recombination probability of the holes and the electrons, and therefore, the regulation and control of the balance of carriers at two ends is key. The main means are as follows: the injection and transmission of holes and electrons are improved, and the recombination probability of the holes and the electrons is further improved; the blocking property of holes and electrons is improved, and the generated excitons are limited in the light-emitting layer, so that high light-emitting efficiency is obtained. Therefore, it is important that the hole transporting material and the electron transporting material perform their functions.

In the organic electroluminescent elements disclosed in the prior art, it has been reported that the driving voltage, efficiency and lifetime of the resulting light-emitting element are improved to some extent by using an arylamine compound as a hole-transporting layer and a pyrimidine compound as an electron-transporting layer, but these are not sufficient and further improvement is required.

Disclosure of Invention

The main object of the present invention is to provide an organic electroluminescent element in which the driving voltage of the light-emitting element is further reduced.

In order to achieve the above object, the present application provides an organic electroluminescent element comprising a hole transporting region, a light emitting layer and an electron transporting region arranged in this order from an anode to a cathode, the hole transporting region containing a compound represented by general formula (1), and the electron transporting region containing a compound represented by general formula (2):

in the general formula (1), R₁To R₈Are the same or different from each other and are each independently hydrogen, deuterium, a substituted or unsubstituted C1-C4 alkyl group, C6-C30 aryl group, or optionally combine with adjacent groups to form a substituted or unsubstituted C1-C4 aryl groupA substituted or unsubstituted ring; ar (Ar)₁And Ar₂Identical or different from one another and each independently is a substituted or unsubstituted aryl radical from C6 to C30, L₁To L₃Are the same or different from each other and are each independently a direct bond, or a substituted or unsubstituted arylene group of C6-C18; in the general formula (2), Py is an unsubstituted pyridyl group; r₉Selected from hydrogen, C1-C4 alkyl or substituted or unsubstituted C6-C18 aryl; ar (Ar)₃Aryl or heteroaryl selected from substituted or unsubstituted C6-C18; l is₄Selected from a direct bond or unsubstituted phenylene; z₁To Z₃At least one of them is N, and the others are CH.

Further, the compound represented by the general formula (1) is represented by any one of the general formulae (1-A), (1-B) and (1-C).

Further, in the compound represented by the general formula (1), R₁To R₈Are both H, L3 is a direct bond, L1 and L2 are direct bonds, Ar₁And Ar₂Is unsubstituted aryl of C6-C25; preferably, the unsubstituted aryl group of C6-C25 is biphenyl, terphenyl, naphthalene, or anthracene; more preferably, the biphenyl is ortho-biphenyl, meta-biphenyl or para-biphenyl.

Further, the compound represented by the general formula (1) is selected from any one of the compounds 1-1 to 1-48.

Further, Py in the nitrogen-containing heterocyclic compound represented by the general formula (2) is pyridyl, R is phenyl, Ar is₃Is phenyl or naphthyl, L is phenylene; preferably, the compound represented by the general formula (2) is selected from any one of the compounds 2-1 to 2-36.

Further, the hole transport region includes any one of a hole injection layer, a hole transport layer, a buffer layer, and an electron blocking layer; or the hole transport region includes any of a hole injection layer, a hole transport layer, a buffer layer, and an electron blocking layer, which are sequentially disposed from the anode to the cathode, wherein at least one layer of the any of the layers contains the compound represented by the general formula (1).

Further, the electron transport region includes any one of an electron injection layer, an electron transport layer, a buffer layer, and a hole blocking layer; or the electron transport region includes any of a hole blocking layer, a buffer layer, an electron transport layer, and an electron injection layer, which are sequentially provided from the anode to the cathode, and at least one of the layers contains the compound represented by the general formula (2).

Further, the light emitting layer is composed of at least a host matrix and a guest dopant.

Further, the host matrix is an anthracene compound represented by general formula (3).

Further, the guest dopant of the light-emitting layer is a fluorescent dye represented by general formula (4).

The organic electroluminescent element provided by the invention adopts the compound represented by the general formula (1) as a hole transport layer, wherein carbazole is substituted at the ortho position of a benzene ring, and the compound is in a conjugated fracture state, so that the organic electroluminescent element has a large band gap, and the energy level of the compound can be adjusted by introducing different substituents; the compound represented by the general formula (2) is further adopted as an electron transport layer, wherein pyridyl and a nitrogen-containing heterocycle are introduced on a phenanthrene ring, so that the electron transport capability of the compound is improved, the thermal stability of the compound is further improved, the energy level of the compound can be adjusted by introducing different substituents on the nitrogen-containing heterocycle, and the combination of the pyridyl and the nitrogen-containing heterocycle is used, so that the voltage of the organic electroluminescent element is reduced, the efficiency is obviously improved, and the service life is obviously improved.

The present application is described in further detail below with reference to specific examples, which should not be construed as limiting the scope of the invention as claimed.

Detailed Description

The present invention will be described in detail with reference to examples, but the scope of the present invention is not limited thereto.

As mentioned in the background art, the driving voltage of the conventional organic electroluminescent device is still relatively high, and in order to further reduce the driving voltage, the present application has studied and screened the matching between the hole transport material and the electron transport material in the conventional organic electroluminescent device, and further found that by matching the hole transport material having a specific structure with the electron transport material having a specific structure, a lower driving voltage can be obtained, thereby obtaining an organic electroluminescent device with further improved device efficiency and lifetime.

On the basis of the above research, the applicant proposes a technical solution of the present application. In a typical embodiment, there is provided an organic electroluminescent element including a hole transporting region, a light emitting layer, and an electron transporting region arranged in this order from an anode to a cathode, the hole transporting region containing a compound represented by general formula (1), and the electron transporting region containing a compound represented by general formula (2):

in the general formula (1), R₁To R₈Are the same or different from each other and are each independently hydrogen, deuterium, substituted or unsubstituted C1-C4 alkyl, C6-C30 aryl, or optionally combine with adjacent groups to form a substituted or unsubstituted ring; ar (Ar)₁And Ar₂Identical or different from one another and each independently is a substituted or unsubstituted aryl radical from C6 to C30, L₁To L₃Are the same or different from each other and are each independently a direct bond, or a substituted or unsubstituted arylene group of C6-C18; in the general formula (2), Py is an unsubstituted pyridyl group; r₉Selected from hydrogen, C1-C4 alkyl or substituted or unsubstituted C6-C18 aryl; ar (Ar)₃Aryl or heteroaryl selected from substituted or unsubstituted C6-C18; l is₄Selected from a direct bond or unsubstituted phenylene; z₁To Z₃At least one of them is N, and the others are CH.

According to the application, through the optimized combination of the hole transport material and the electron transport material, the compound shown in the general formula (1) is good in thermal stability and excellent in hole transport capability, the compound shown in the general formula (3) contains planar groups of phenanthryl, pyridyl and triazine electronegative groups, the molecular structure is large in steric hindrance and not easy to crystallize, the thermal stability is improved, the electron transport capability is excellent, and the combination of the two is more beneficial to the injection and transport of holes and electrons on two sides and the balanced recombination in a light emitting layer, so that the device efficiency is improved.

In a preferred embodiment, the compound represented by the general formula (1) is represented by any one of the following general formulae (1-A), (1-B) and (1-C):

in the general formulae (1-A), (1-B) and (1-C), R₁To R₈、Ar₁And Ar₂、L₁To L₃The same as defined in the general formula (1).

In a preferred embodiment, in the compounds represented by the general formulae (1-A), (1-B) and (1-C), R₁To R₈Are both H, L3 is a direct bond, L1 and L2 are direct bonds, Ar₁And Ar₂Is unsubstituted aryl of C6-C25; preferably, the unsubstituted aryl group of C6-C25 is biphenyl, terphenyl, naphthalene or anthracene; more preferably, the biphenyl is ortho-biphenyl, meta-biphenyl or para-biphenyl.

In a preferred embodiment, in the compound represented by the general formula (1), R is₁To R₈Are both H, L3 is a direct bond, L1 and L2 are direct bonds, Ar₁And Ar₂Is unsubstituted aryl of C6-C25; preferably, the unsubstituted aryl group of C6-C25 is biphenyl, terphenyl, naphthalene, or anthracene; more preferably, the biphenyl is ortho-biphenyl, meta-biphenyl, or para-biphenyl.

In a preferred embodiment, the compound represented by the general formula (1) is selected from any one of the following:

in a preferred embodiment, Py in the nitrogen-containing heterocyclic compound represented by the general formula (2) is pyridyl, R is phenyl, Ar is₃Is phenyl or naphthyl, L is phenylene; more preferably, the compound represented by the general formula (2) is selected from any one of the following:

in the above organic electroluminescent element, the hole transporting region may be one layer or a plurality of layers. When it is one layer, the hole transport region includes any one of a hole injection layer, a hole transport layer, a buffer layer, and an electron blocking layer; when it is a multilayer, the hole transport region includes any of a hole injection layer, a hole transport layer, a buffer layer, and an electron blocking layer, which are provided in this order from the anode to the cathode, wherein at least one of the layers contains the compound represented by the general formula (1).

Similarly, in the above organic electroluminescent element, the electron transporting region may be one layer or a plurality of layers. When it is one layer, the electron transport region includes any one of an electron injection layer, an electron transport layer, a buffer layer, and a hole blocking layer; when the electron transporting region includes a plurality of layers, it includes any of a hole blocking layer, a buffer layer, an electron transporting layer, and an electron injecting layer, which are sequentially provided from the anode to the cathode, wherein at least one of the plurality of layers contains the compound represented by the general formula (2).

In the organic electroluminescent element, the luminescent layer is formed by blending at least one host matrix and one guest dopant. The particular host matrix and guest dopant species may be matched from available materials with appropriate choice. In a preferred embodiment of the present invention, the organic electroluminescent element has a host matrix of an anthracene compound represented by general formula (3),

wherein R is₁₁And R₁₂Are the same or different from each other and are each independently hydrogen, substituted or unsubstituted alkyl of C1-C6, alkoxy, aryl or heteroaryl of C6-C30; ar (Ar)₄、Ar₅Each independently is selected from phenyl, biphenyl, naphthyl, anthryl, phenanthryl, naphthacenyl or pyrenyl; a. b, c are each an integer of 1 to 4, and when a, b, c are each an integer of 2 or more, two or more structures in parentheses are the same as or different from each other.

In another preferred embodiment of the present application, in the above organic electroluminescent element, the guest dopant of the light-emitting layer is a fluorescent dye represented by formula (4),

wherein Ar is₆And Ar₇Are identical or different from one another and are each independently substituted or unsubstituted silyl, aryl or heteroaryl of C6-C30, or form a substituted or unsubstituted ring with one another; ar (Ar)₈Is substituted or unsubstituted benzofluorenyl, fluoranthenyl, pyrenyl orA group; l is₅Is a direct bond, a substituted or unsubstituted arylene or heteroarylene group of C6-C18; n is an integer of 1 to 4, and when n is an integer of 2 or more, two or more structures in parentheses are the same as or different from each other.

The selection of the host and guest as described above is not particularly advantageous as long as the application of blue fluorescence can be achieved. According to the application, through the optimized combination of the hole transport material and the electron transport material, the compound shown in the general formula (1) is good in thermal stability and excellent in hole transport capacity, and the compound shown in the general formula (3) contains planar groups of phenanthryl, pyridyl and triazine electronegative groups, so that the molecular structure is large in steric hindrance and difficult to crystallize, the thermal stability is improved, the electron transport capacity is excellent, and the combination of the two is more beneficial to the injection and the transmission of holes and electrons on two sides and the balanced recombination in a light emitting layer, so that the device efficiency is improved.

The compound serving as an electron-transporting region described above in the present application may be used in any combination with the compound serving as a hole-transporting region, and for example, any combination of any of the compounds 1-1 to 1-48 and any of the compounds 2-1 to 2-36 may be used. In a preferred embodiment, compounds 1-1, 1-4, 1-11, 1-18, 1-26, 1-47 and compounds 2-1, 2-2, 2-3, 2-4, 2-5, 2-6, 2-7, 2-8, 2-9, 2-10, 2-11, 2-12, 2-13, 2-14, 2-15, 2-16, 2-17, 2-18, 2-19, 2-20, 2-21, 2-22, 2-23, 2-24, 2-25, 2-26, 2-27, 2-28, 2-29, 2-30, 2-31, 2-32, 2-33, 2-34, 2-35 and 2-36 in any combination.

The following examples are provided to further illustrate the benefits of the present application.

A first part:

1. preparation of hole transport layer materials

1.1 Synthesis of Compound 1-1

Reacting 9- (4 '-chloro [1,1' -biphenyl)]-2-yl) -9H-carbazole (21.2g, 60mmol), bis- (4-biphenylyl) amine (19.3g, 60.6mmol), 210mL of toluene, 8.48g of sodium tert-butoxide are added to a 500mL round-bottom flask, stirred under nitrogen and warmed to 50 ℃, 0.27g of catalyst Pd is added₂(dba)₃And 7.5g of a 10% solution of tri-tert-butylphosphine in toluene, with further addition of the solventThe reaction is stopped after the temperature is heated to reflux reaction for 4 hours, 40mL of water solution is added after the temperature is reduced, organic phase is heated, toluene is refluxed, dewatered and dried, then the mixture is decolored by a short silica gel column, half of toluene is evaporated in a rotary mode, the temperature is reduced to 70 ℃, 50mL of normal hexane is added, solid is separated out by stirring and cooling, and 32.9g of white solid compound 1-1 is obtained after filtration and drying, and the yield is 81.4%. The compound 1-1 is further purified twice by vacuum sublimation with a purity of 99.97% MS [ M + H ]]+＝638.25。

1.2 Synthesis of Compounds 1-4

Reacting 9- (4 '-chloro [1,1' -biphenyl)]-2-yl) -9H-carbazole (21.2g, 60mmol), N- (1, 1-biphenyl) -1,1 '. 4' -terphenyl) amine (24.1g, 60.6mmol), 210mL of toluene, 8.48g of sodium tert-butoxide, were added to a 500mL round bottom flask, stirred under nitrogen and warmed to 50 deg.C, 0.27g of catalyst Pd was added₂(dba)₃And 7.5g of 10% toluene solution of tri-tert-butylphosphine, continuously heating until the reflux reaction is carried out for 4 hours, stopping the reaction, cooling, adding 40mL of water solution, carrying out organic phase heating, carrying out reflux dehydration and drying on toluene, decoloring by a short silica gel column, carrying out rotary evaporation on half toluene, cooling to 70 ℃, adding 50mL of n-hexane, stirring, cooling to separate out a solid, filtering and drying to obtain 36.1g of white solid compound 1-4, wherein the yield is 79.6%. The compound 1-4 is further purified twice by vacuum sublimation with purity of 99.98% MS [ M + H ]]+＝714.34。

1.3 Synthesis of Compounds 1-11

Reacting 9- (4 '-chloro [1,1' -biphenyl)]-2-yl) -9H-carbazole (21.2g, 60mmol), bis (9, 9-dimethyl-9H-fluoren-2-yl) amine (24.3g, 60.6mmol), 210mL of toluene, 8.48g of sodium tert-butoxide are added to a 500mL round-bottom flask, the temperature is raised to 50 ℃ with stirring under nitrogen protection, 0.27g of catalyst Pd is added₂(dba)₃And 7.5g of a 10% solution of tri-tert-butylphosphine in toluene, and heating to refluxAnd stopping the reaction after reacting for 4 hours, cooling, adding 40mL of water solution, adding organic phase hot toluene, refluxing, dewatering and drying, decoloring by using a short silica gel column, then performing rotary evaporation to remove half of toluene, cooling to 70 ℃, adding 50mL of n-hexane, stirring, cooling to precipitate a solid, filtering and drying to obtain 35.7g of white solid compound 1-11, wherein the yield is 78.5%. The compound 1-11 is further purified twice by vacuum sublimation with a purity of 99.97% MS [ M + H ]]+＝718.37。

1.4 Synthesis of intermediate A1

In a 500mL two-necked flask, 11H-benzo [ c ] carbazole (13.2g, 60mmol), copper iodide (11.4g, 60mmol), and potassium carbonate (16.6g, 120mmol) were charged, followed by addition of 4-chloro-4 '-iodo-1, 1' -biphenyl (37.7g, 120mmol) and 200mL of xylene under nitrogen protection, and the reaction was stirred at 185 ℃ for 72H. After the reaction was completed, the reaction mixture was cooled and filtered to remove copper powder, then xylene was removed by heating and rotary evaporation under reduced pressure, and then purified by column chromatography to obtain 31.2g of white intermediate A1 in 61.3% yield.

1.5 Synthesis of intermediate A2

In a 500mL two-necked flask, 5H-benzo [ b ] carbazole (13.2g, 60mmol), copper iodide (11.4g, 60mmol), and potassium carbonate (16.6g, 120mmol) were charged, followed by addition of 4-chloro-4 '-iodo-1, 1' -biphenyl (37.7g, 120mmol) and 200mL of xylene under nitrogen protection, and the reaction was stirred at 185 ℃ for 72H. After the reaction was completed, the reaction mixture was cooled and filtered to remove copper powder, then xylene was removed by heating and rotary evaporation under reduced pressure, and then 32.7g of white intermediate A2 was obtained through column chromatography purification, with a yield of 64.2%.

1.6 Synthesis of intermediate A3

In a 500mL two-necked flask, 7H-benzo [ c ] carbazole (13.2g, 60mmol), copper iodide (11.4g, 60mmol), and potassium carbonate (16.6g, 120mmol) were added, followed by addition of 4-chloro-4 '-iodo-1, 1' -biphenyl (37.7g, 120mmol) and 200mL of xylene under nitrogen protection, and the reaction was stirred at 185 ℃ for 72H. After the reaction was completed, the reaction mixture was cooled, filtered to remove copper powder, heated under reduced pressure and rotary distilled to remove xylene, and then purified by column chromatography to obtain 32.3g of white intermediate A3 in 63.5% yield.

1.7 Synthesis of Compounds 1 to 18

Intermediate A1(24.2g, 60mmol), N- [1,1' -biphenyl]-4-yl-9, 9-dimethyl-9H-fluoren-2-amine (21.9g, 60.6mmol), 210mL of toluene, 8.48g of sodium tert-butoxide are added to a 500mL round-bottom flask, stirred under nitrogen and warmed to 50 ℃ and 0.27g of catalyst Pd is added₂(dba)₃And 7.5g of 10% toluene solution of tri-tert-butylphosphine, continuously heating until reflux reaction is carried out for 4 hours, stopping the reaction, cooling, adding 40mL of water solution, adding organic phase heated toluene, refluxing, dewatering, drying, decoloring by a short silica gel column, carrying out rotary evaporation to obtain half toluene, cooling to 70 ℃, adding 50mL of n-hexane, stirring, cooling to separate out a solid, filtering, and drying to obtain 35.6g of white solid compound 1-18, wherein the yield is 77.2%. The compounds 1-18 were further purified twice by vacuum sublimation to a purity of 99.99%, MS [ M + H ]]+＝728.36。

1.8 Synthesis of Compounds 1-26

Intermediate A2(24.2g, 60mmol), bis ([1,1' -biphenyl ] yl)]-3-yl) amine (19.5g, 60.6mmol), 210mL toluene, 8.48g sodium tert-butoxide are added to a 500mL round-bottom flask, stirred under nitrogen and warmed to 50 deg.C, 0.27g Pd catalyst is added₂(dba)₃And 7.5g of a 10% solution of tri-tert-butylphosphine in toluene, and the temperature was further raised toAnd stopping the reaction after the reflux reaction is carried out for 4 hours, cooling, adding 40mL of water for liquid separation, adding organic phase heated toluene, refluxing, removing water, drying, decoloring by a short silica gel column, carrying out rotary evaporation to remove half of toluene, cooling to 70 ℃, adding 50mL of n-hexane, stirring, cooling to precipitate a solid, filtering and drying to obtain 34.6g of white solid compounds 1-26 with the yield of 79.1%. The compounds 1-18 were further purified twice by vacuum sublimation with a purity of 99.98% MS [ M + H ]]+＝688.28。

1.9 Synthesis of Compounds 1-47

Intermediate A3(24.2g, 60mmol), bis (9, 9-dimethyl-9H-fluoren-2-yl) amine (24.3g, 60.6mmol), 210mL toluene, 8.48g sodium tert-butoxide were added to a 500mL round-bottomed flask, stirred under nitrogen and warmed to 50 deg.C, 0.27g catalytic Pd was added₂(dba)₃And 7.5g of 10% toluene solution of tri-tert-butylphosphine, continuously heating until reflux reaction is carried out for 4 hours, stopping the reaction, cooling, adding 40mL of water solution, adding organic phase hot toluene, refluxing, dehydrating, drying, decoloring by a short silica gel column, then rotationally evaporating out half toluene, cooling to 70 ℃, adding 50mL of n-hexane, stirring, cooling to separate out a solid, filtering and drying to obtain 37.7g of white solid compounds 1-47, wherein the yield is 77.8%. The compounds 1-47 were further purified twice by vacuum sublimation with a purity of 99.98% MS [ M + H ]]+＝768.42。

2. Preparation of Electron transport layer materials

2.1 Synthesis of intermediate B

1-bromo-2-iodobenzene (70.7g, 250mmol), phenylacetylene (25.5g, 250mmol) and 350mL triethylamine were added to a three-necked flask, and after a nitrogen blanket of 10min, CuI (0.48g, 2.5mmol) and 0.7g Pd (PPh) were added₃)₂Cl₂Stirring at room temperature for 0.5 hr, stopping reaction, filtering to obtain a large amount of solid, leaching with triethylamine, and concentrating at below 35 deg.CTriethylamine was removed, dissolved in 100mL of dichloromethane, washed with dilute hydrochloric acid solution to near neutrality, and concentrated to dryness to give 46.8g of B1 as a yellow oil in 96% yield.

B1(15.4g, 60mmol), 4-chlorobenzeneboronic acid (10.3g, 66mmol) and potassium carbonate (16.6g, 120mmol) were added to a three-necked flask, 90mL of toluene, 45mL of THF and 45mL of deionized water were added thereto, and after nitrogen-purged for 10min, 0.31g of Pd (PPh) was added₃)₂Cl₂Heating to reflux, reacting for 5h, cooling, separating, washing with water to neutrality, performing rotary evaporation concentration, adding ethanolamine phosphate to dissolve, passing through a silica gel column, leaching with ethanolamine phosphate, and performing rotary evaporation concentration to obtain 18.2g of yellow oily liquid B2 with the yield of 71%.

Adding B2(14.5g, 60mmol) and 350mL of dichloromethane into a three-neck flask, cooling to 0 ℃ in an ice bath, dissolving 11.6g of iodine chloride in 90mL of dichloromethane, dropwise adding into the three-neck flask (dropwise adding for 0.5h), stirring for reacting for 0.5h, dropwise adding a sodium sulfite solution to quench the reaction to neutrality, separating, drying, concentrating by rotary evaporation, passing through a silica gel column with ethanolamine phosphate, concentrating by rotary evaporation, and drying to obtain 15.6g of light yellow green solid B3 with the yield of 54%.

B3(17.3g, 35mmol), 3-pyridineboronic acid pinacol ester (10.9g, 53mmol) and potassium carbonate (14.5g, 105mmol) were added to a three-necked flask, 105mL of toluene, 35mL of ethanol and 35mL of deionized water were added, and after 10min under nitrogen, 0.87g of Pd (PPh) was added₃)₂Cl₂Heating and refluxing, reacting for 6h, cooling, separating liquid, washing with water, precipitating solid, filtering, washing with water to neutrality, washing with ethanol, and drying. And (3) dissolving 200Ml of toluene, passing through a silica gel column while the solution is hot, leaching with dichloromethane, performing rotary evaporation and concentration to about 50mL, cooling and crystallizing, and drying to obtain 10.7g of light yellow solid B with the yield of 38%.

2.2 Synthesis of intermediate C

Intermediate B (18.3g, 50mmol), pinacol diboron (15.2g, 60mmol), potassium acetate (14.7g, 150mmol) and 180mL dioxaneThe alkane was placed in a 500ml round bottom flask and stirred while heating. Adding Pd (dba) under reflux₂(0.57g, 1mmol) and tricyclohexylphosphine (0.56g, 2mmol) and stirred for 6 hours. After cooling to normal temperature, 50ml of water was added and stirred. The organic layer was separated, dried over anhydrous magnesium sulfate, then concentrated by rotary evaporation, and purified through a silica gel column to give 21.8g of intermediate C in 65% yield.

2.3 Synthesis of Compound 2-3

C (11.7g, 25mmol), 2-bromo-4, 6-diphenyl-1, 3, 5-triazine (7.8g, 25mmol), potassium carbonate (13.8g, 100mmol), tetrakis (triphenylphosphine) palladium (0.58g, 0.5mmol), 150mL of tetrahydrofuran and 75mL of water were added to a 500mL round bottom flask, stirred at reflux for 8h, cooled to room temperature, the organic layer was separated, then concentrated by rotary evaporation, and purified over a silica gel column to give 20.1g of the product 2-3 as a white solid in 68% yield. The product 2-3 was further purified twice by vacuum sublimation with a purity of 99.96% and MS [ M + H ] + ═ 562.32.

2.4 Synthesis of Compounds 2-9

B (7.3g, 20mmol), (3- (4, 6-diphenyl-1, 3, 5-triazine-2-) phenyl) boronic acid (7.4g, 21mmol), potassium carbonate (8.3g, 60mmol) were added to a three-necked flask, 70mL of toluene, 35mL of THF, and 35mL of deionized water were added thereto, and after nitrogen was purged for 10min, 0.22g of Pd (OAc) was added₂And 0.44g X-phos, heating to 78 ℃ for reaction for 1h, precipitating a large amount of solid, filtering while hot, washing with water to be nearly neutral, washing with ethanol and drying, refluxing and dissolving with 150mL of dichloromethane, passing through silica gel, leaching with dichloromethane, concentrating to about 50mL, stirring at room temperature for crystallization, filtering, and leaching with dichloromethane. The resulting filter cake was recrystallized from 150mL of dichloromethane to give 3.4g of the product 2-9 as a white solid in 23% yield. The product 2-9 is further purified twice by vacuum sublimation with a purity of 99.96% MS [ M + H ]]+＝638.16。

2. Thermodynamic properties of compounds

The glass transition temperature Tg is determined by differential scanning calorimetry (DSC, DSC25 differential scanning calorimeter from TA of America), the temperature rise rate is 10 ℃/min; the decomposition temperature Td is a temperature at which 1% weight loss occurs in a nitrogen atmosphere, and is measured on a TGA55 thermogravimetric analyzer (TA, USA) with a nitrogen flow rate of 20mL/min, and the specific data are shown in Table 1 below.

Table 1:

compound (I)	Tg(℃)	Td(℃)
			1-1	116	382
1-4	119	389
			1-11	125	396
1-18	131	405
			1-26	122	391
1-47	134	411
			2-3	139	350
2-9	145	366

As is clear from the data in the table, the glass transition temperatures of the compound represented by the general formula (1) and the compound represented by the general formula (2) used in the present invention are both 100 ℃ or higher, and they are hardly decomposed and excellent in thermal stability.

A second part: preparation of organic electroluminescent element

Practical effects of the organic electroluminescent element of the present invention prepared using the compound represented by the general formula (1) as the material for the hole transporting region and the compound represented by the general formula (2) as the material for the electron transporting region in combination are described in detail below by way of specific examples and comparative examples.

The structural formula of the organic material used is as follows:

example 1

The method for manufacturing the organic electroluminescent element by using the Sunic sp1710 evaporator comprises the following specific steps: a glass substrate (Corning glass 40mm 0.7mm) coated with 135nm thick ITO (indium tin oxide) was treated with isopropanol and pure water, respectivelyUltrasonically washing the glass substrate for 5 minutes by water, cleaning the glass substrate by using ultraviolet and ozone, and then conveying the glass substrate into a vacuum deposition chamber; the hole transport material HT1 doped with 4% HD was evacuated at a thickness of 20nm (about 10nm)^-7Torr) is thermally deposited on the transparent ITO electrode to form a hole injection layer; vacuum depositing compound 1-1 with a thickness of 60nm on the hole injection layer as a first hole transport layer; then, vacuum depositing a second hole transport layer HT 2; then vacuum depositing BH with doping mass fraction of 4% BD of 25nm as a light emitting layer; then depositing a compound 2-3 doped with 50% LiQ (8-hydroxyquinoline lithium) in vacuum to form an electron transport layer with the thickness of 30 nm; finally depositing metal ytterbium (Yb, an electron injection layer) with the thickness of 2nm and magnesium-silver alloy with the doping ratio of 10:1 in sequence to form a cathode; the components are finally transferred from the deposition chamber into a glove box, where they are then encapsulated with a UV curable epoxy resin and a glass cover plate containing a moisture absorber.

In the above manufacturing steps, the deposition rates of the organic material, ytterbium metal and Mg metal were maintained at 0.1nm/s, 0.05 nm/s and 0.2nm/s, respectively.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-1(60nm)/HT2(10 nm)/BH: 4% BD (25 nm)/Compound 2-3: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 2

An experiment was performed in the same manner as in example 1 except that: compounds 1-4 were used as the first hole transport layer.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-4(60nm)/HT2(10 nm)/BH: 4% BD (25 nm)/Compound 2-3: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 3

An experiment was performed in the same manner as in example 1 except that: compounds 1-11 were used as the first hole transport layer.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-11(60nm)/HT2(10 nm)/BH: 4% BD (25 nm)/Compound 2-3: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 4

An experiment was performed in the same manner as in example 1 except that: compounds 1-18 were used as the first hole transport layer.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-18(60nm)/HT2(10 nm)/BH: 4% BD (25 nm)/Compound 2-3: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 5

An experiment was performed in the same manner as in example 1 except that: compounds 1-26 were used as the first hole transport layer.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-26(60nm)/HT2(10 nm)/BH: 4% BD (25 nm)/Compound 2-3: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 6

An experiment was performed in the same manner as in example 1 except that: compounds 1-47 were used as the first hole transport layer.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-47(60nm)/HT2(10 nm)/BH: 4% BD (25 nm)/Compound 2-3: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 7

An experiment was performed in the same manner as in example 1 except that: compounds 1 to 11 were used as the first hole transporting layer, and compounds 2 to 9 were used as the electron transporting layer.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-11(60nm)/HT2(10 nm)/BH: 4% BD (25 nm)/Compound 2-9: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 8

An experiment was performed in the same manner as in example 1 except that: compounds 1 to 18 were used as the first hole transporting layer, and compounds 2 to 9 were used as the electron transporting layer.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-18(60nm)/HT2(10 nm)/BH: 4% BD (25 nm)/Compound 2-9: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 9

An experiment was performed in the same manner as in example 1 except that: compounds 1 to 26 were used as the first hole transporting layer, and compounds 2 to 9 were used as the electron transporting layer.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-26(60nm)/HT2(10 nm)/BH: 4% BD (25 nm)/Compound 2-9: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 10

An experiment was performed in the same manner as in example 1 except that: compounds 1 to 47 were used as the first hole transporting layer, and compounds 2 to 9 were used as the electron transporting layer.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-47(60nm)/HT2(10 nm)/BH: 4% BD (25 nm)/Compound 2-9: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 11

An experiment was performed in the same manner as in example 1 except that: compounds 1 to 4 were used as the first hole transporting layer, and compounds 1 to 11 were used as the second hole transporting layer in place of HT 2.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-4(60 nm)/Compound 1-11(10nm)/BH: 4% BD (25 nm)/Compound 2-3: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 12

An experiment was performed in the same manner as in example 1 except that: compounds 1 to 4 were used as the first hole transporting layer, and compounds 1 to 18 were used as the second hole transporting layer in place of HT 2.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-4(60 nm)/Compound 1-18(10nm)/BH: 4% BD (25 nm)/Compound 2-3: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 13

An experiment was performed in the same manner as in example 1 except that: compounds 1 to 4 were used as the first hole transporting layer, and compounds 1 to 47 were used as the second hole transporting layer in place of HT 2.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20 nm)/Compound 1-4(60 nm)/Compound 1-47(10 nm)/BH: 4% BD (25 nm)/Compound 2-3: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 14

An experiment was performed in the same manner as in example 1 except that: while compounds 1 to 4 were used instead of HT1 as the hole injection layer host and the first hole transport layer, compounds 1 to 11 were used instead of HT2 as the second hole transport layer.

The element structure is represented as: ITO (135 nm)/compound 1-4: 4% HD (20 nm)/compound 1-4(60 nm)/compound 1-11(10nm)/BH: 4% BD (25 nm)/compound 2-3: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Example 15

An experiment was performed in the same manner as in example 1 except that: while compounds 1 to 4 were used instead of HT1 as the hole injection layer host and the first hole transport layer, compounds 1 to 18 were used instead of HT2 as the second hole transport layer.

The element structure is represented as: ITO (135 nm)/compound 1-4: 4% HD (20 nm)/compound 1-4(60 nm)/compound 1-18(10nm)/BH: 4% BD (25 nm)/compound 2-3: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

Comparative example 1

An experiment was performed in the same manner as in example 1 except that: compound HT1 was used as the first hole transporting layer instead of compound 1-1, and compound ET was used as the electron transporting layer instead of compound 2-3.

The element structure is represented as: ITO (135nm)/HT1: 4% HD (20nm)/HT1(60nm)/HT2(10nm)/BH: 4% BD (25nm)/ET: LiQ (5:5,30nm) Yb (2nm)/Mg: Ag (10:1,150 nm).

The luminance, luminous efficiency, EQE (external quantum efficiency) of the light-emitting element were measured by fradah FS-100GA4, su, and the device lifetime LT95 (time taken for the initial luminance to 4000nits, decay to 3800 nits) was measured by fradah FS-MP96, all measurements being performed in a room temperature atmosphere. The light emitting element was at 10mA/cm²Specific properties of operating voltage (V), current efficiency (C.E.), External Quantum Efficiency (EQE), and color coordinates (CIEx, CIEy) at current densityThe data are shown in Table 2.

Table 2:

as can be seen from the table, the above-described embodiments of the present invention achieve the following technical effects: compared with comparative example 1, the devices of examples 1 to 15 have reduced driving voltage, improved efficiency and significantly increased lifetime, which shows that the compound represented by the general formula (1) improves the hole transport rate as the first hole transport layer, and the compound represented by the general formula (2) improves the electron transport rate as the electron transport layer, and the combination of the two promotes effective recombination of holes and electrons, thereby improving the device efficiency. In addition, the device lifetime is also improved due to the excellent thermal stability of both.

On the basis, in examples 11 to 13, the compound represented by the general formula (1) is simultaneously used as the second hole transport layer, the interface between the first hole transport layer and the second hole transport layer is optimized, and the efficiency and the lifetime of the device are improved compared with those of example 2. On the basis of example 11 and example 12, in example 14 and example 15, the compound represented by the general formula (1) is further used as a hole injection layer, and hole injection is optimized, so that the efficiency and the lifetime of the device are further improved.

The above description is only a preferred embodiment of the present invention and is not intended to limit the present invention, and various modifications and changes may be made by those skilled in the art. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention should be included in the protection scope of the present invention.