Organic electroluminescent device

Abstract

An organic electroluminescent device includes: a first electrode; a second electrode; and an organic layer formed between the first electrode and the second electrode, the organic layer including a light-emitting layer formed using a solution containing an organic electroluminescent material and a solvent, the organic electroluminescent material containing a host and a dopant, the host containing one or more compounds represented by the following [Chemical Formula A], the dopant containing one or more compounds represented by the following [Chemical Formula A], the dopant containing one or more compounds represented by the following [Chemical Formula A], and the organic layer containing one or more compounds represented by the following [Chemical Formula B]. The dopant contains one or more compounds represented by the following [Chemical Formula B-1] or [Chemical Formula B-2]. [Chemical Formula A] # imgabs0 # # imgabs1 #

Description

Technical Field

[0001] The present invention relates to an organic electroluminescent device, and more particularly, to an organic electroluminescent device in which operating characteristics of the device such as luminous efficiency, driving voltage, and lifespan are improved by including an organic electroluminescent material having high solubility in a solvent.

[0002] For reference, the present invention is part of a research project of the Korea Institute of Industrial Technology Evaluation and Management under the Ministry of Trade, Industry and Energy of Korea, which aims to establish future growth drivers for the materials and components industries - display innovation process platform. It is the research result of SFC Co., Ltd. under the project name "Development of High-performance, Long-life Emissive Layer Ink Materials and Device Technology for Printing Processes" (Project No.: 20011059). The research period was from April 1, 2020 to December 31, 2024. Background Art

[0003] An organic electroluminescent device is a display device that utilizes the self-luminous phenomenon. It has a large viewing angle, can be thinner, lighter, and shorter than a liquid crystal display, and has advantages such as a fast response speed. Therefore, it is used as a full-color display or lighting.

[0004] Generally, the organic light-emitting phenomenon refers to the phenomenon of converting electrical energy into light energy using an organic substance. An organic electroluminescent device using the organic light-emitting phenomenon usually has a structure including an anode, a cathode, and an organic layer therebetween. Among them, in order to improve the luminous efficiency and stability of the organic electroluminescent device, the organic layer is usually composed of a multi-layer structure of different substances. For example, it can be composed of a hole injection layer, a hole transport layer, a light-emitting layer, an electron transport layer, an electron injection layer, etc. In the structure of such an organic electroluminescent device, when a voltage is applied between the two electrodes, holes are injected from the anode, and electrons are injected from the cathode into the organic layer. When the injected holes and electrons meet, excitons are formed. When the excitons fall back to the ground state, light is emitted. Such an organic light-emitting device is known to have characteristics such as self-luminance, high brightness, high luminous efficiency, low driving voltage, wide viewing angle, high contrast, and high-speed response.

[0005] Currently, displays are becoming larger and larger. When manufacturing large displays using a deposition process, there are disadvantages such as a decrease in production yield and an increase in investment costs as the substrate becomes larger. In addition, since the deposition process evaporates single-molecule substances under vacuum conditions and deposits them on the substrate, in order to prevent decomposition at the high evaporation temperature, substances with a high glass transition temperature need to be used, so there are limitations.

[0006] On the other hand, when manufacturing a large display by preparing a solution by dissolving an organic electroluminescent material in a solvent and then coating the solution on a substrate, it has advantages such as lower process costs than the deposition process and relatively simple process steps. However, organic electroluminescent materials generally have low solubility in solvents, so it is difficult to ensure the luminous efficiency, brightness, power efficiency, lifespan, and thermal stability of the device.

[0007] Therefore, there is a continuous need to develop organic electroluminescent materials that have high solubility in solvents and can improve the luminous efficiency, brightness, power efficiency, lifespan, and thermal stability of the device. Summary of the Invention

[0008] Technical Problem

[0009] In order to solve the problems described above, an object of the present invention is to provide an organic electroluminescent device that has a lower driving voltage, improved luminous efficiency, and improved lifespan characteristics by using an organic electroluminescent material with high solubility in a solvent.

[0010] The problems to be solved by the present invention are not limited to the problems described above, and those skilled in the art can clearly understand other problems not mentioned from the following description.

[0011] Technical Solution

[0012] <1> The organic electroluminescent device of the present invention is an organic electroluminescent device including a first electrode, a second electrode, and an organic layer formed between the first electrode and the second electrode. The organic layer may include a light-emitting layer formed using a solution containing an organic electroluminescent material and a solvent. The organic electroluminescent material may include a host and a dopant. The host may include one or more compounds represented by the following [Chemical Formula A], and the dopant may include one or more compounds represented by the following [Chemical Formula B-1] or [Chemical Formula B-2].

[0013] [Chemical Formula A]

[0014]

[0015] In the [Chemical Formula A],

[0016] L1 and L2 are the same as or different from each other and are each independently selected from the group consisting of a substituted or unsubstituted alkylene group having 1 to 20 carbon atoms, a substituted or unsubstituted arylene group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroarylene group having 3 to 30 carbon atoms.

[0017] The Rs are the same as or different from each other, and each independently is selected from the group consisting of a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylthioxy group having 1 to 30 carbon atoms, a substituted or unsubstituted arylthioxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylamino group having 6 to 30 carbon atoms, a substituted or unsubstituted heteroarylamino group having 2 to 30 carbon atoms, a substituted or unsubstituted diarylamino group having 12 to 24 carbon atoms, a substituted or unsubstituted diheteroarylamino group having 2 to 24 carbon atoms, a substituted or unsubstituted aryl(heteroaryl)amino group having 7 to 24 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms, a substituted or unsubstituted alkylsilyl group having 1 to 30 carbon atoms, and a substituted or unsubstituted arylsilyl group having 6 to 30 carbon atoms.

[0018] Ar1 and Ar2 are the same as or different from each other, and each independently is selected from the group consisting of a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 50 carbon atoms.

[0019] The n is an integer from 0 to 8. When n is 2 or more, each R is the same as or different from each other.

[0020] The n1 and n2 are each independently an integer from 1 to 3.

[0021] The A1 is a substituted or unsubstituted aryl group having 10 to 30 carbon atoms.

[0022]

[0023] In the [Chemical Formula B-1] and [Chemical Formula B-2],

[0024] The T1 to T3 are the same as or different from each other, and each independently is an aromatic hydrocarbon ring having 6 to 50 carbon atoms or an aromatic heterocyclic ring having 2 to 40 carbon atoms.

[0025] The T1 to T3 can each independently be substituted by at least one R T When substituted by two or more Rs T substituted, these Rs Tsame as or different from each other,

[0026] said R T is selected from any one of the group consisting of hydrogen, deuterium atom, substituted or unsubstituted alkyl having 1 to 30 carbon atoms, substituted or unsubstituted alkenyl having 2 to 30 carbon atoms, substituted or unsubstituted alkynyl having 2 to 24 carbon atoms, substituted or unsubstituted aryl having 6 to 50 carbon atoms, substituted or unsubstituted cycloalkyl having 3 to 30 carbon atoms, substituted or unsubstituted cycloalkenyl having 5 to 30 carbon atoms, substituted or unsubstituted heteroaryl having 2 to 50 carbon atoms, substituted or unsubstituted alkoxy having 1 to 30 carbon atoms, substituted or unsubstituted aryloxy having 6 to 30 carbon atoms, substituted or unsubstituted alkylthioxy having 1 to 30 carbon atoms, substituted or unsubstituted arylthioxy having 5 to 30 carbon atoms, -N(R”)2, substituted or unsubstituted alkylsilyl having 1 to 30 carbon atoms, substituted or unsubstituted arylsilyl having 5 to 30 carbon atoms, cyano and halogen,

[0027] said R”s are same as or different from each other and each independently selected from the group consisting of hydrogen atom, deuterium atom, substituted or unsubstituted alkyl having 1 to 30 carbon atoms, substituted or unsubstituted alkenyl having 2 to 30 carbon atoms, substituted or unsubstituted cycloalkyl having 3 to 30 carbon atoms, substituted or unsubstituted cycloalkenyl having 5 to 30 carbon atoms, substituted or unsubstituted aryl having 6 to 50 carbon atoms and substituted or unsubstituted heteroaryl having 3 to 50 carbon atoms, and said R”s can combine with each other to form an alicyclic or aromatic monocyclic or polycyclic ring,

[0028] said Y1 is selected from any one of the group consisting of N-R 11 、CR 12 R 13 、O、S and SiR 14 R 15 and the like,

[0029] said Y2 is selected from any one of the group consisting of N-R 16 、CR 17 R 18 、O、S and SiR 19 R 20 and the like,

[0030] said Y3 is selected from any one of the group consisting of N-R 21 、CR 22 R 23 、O、S and SiR 24 R 25 and the like,

[0031] said R 11to R 25 each is the same as or different from one another, and each is independently selected from the group consisting of a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted heteroaryl group having 2 to 50 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylthioxy group having 1 to 30 carbon atoms, a substituted or unsubstituted arylthioxy group having 5 to 30 carbon atoms, a substituted or unsubstituted alkylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylamino group having 6 to 30 carbon atoms, a substituted or unsubstituted heteroarylamino group having 2 to 30 carbon atoms, a substituted or unsubstituted diarylamino group having 12 to 24 carbon atoms, a substituted or unsubstituted diheteroarylamino group having 2 to 24 carbon atoms, a substituted or unsubstituted aryl(heteroaryl)amino group having 7 to 24 carbon atoms, a substituted or unsubstituted alkylsilyl group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsilyl group having 5 to 30 carbon atoms, a cyano group, and a halogen, and the R 11 to R 25 each can bind to one or more rings selected from the group consisting of the T1 to T3 to further form an alicyclic or aromatic monocyclic or polycyclic ring.

[0032] <2> In the <1> above,

[0033] in the [Chemical Formula A], A1 can be any one selected from the group consisting of the groups represented by the following [Chemical Formula A-1] to [Chemical Formula A-4]:

[0034]

[0035] In the [Chemical Formula A-1] to [Chemical Formula A-4],

[0036] R1 to R4 are the same as or different from each other, and each independently is selected from the group consisting of a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylthioxy group having 1 to 30 carbon atoms, a substituted or unsubstituted arylthioxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylamino group having 6 to 30 carbon atoms, a substituted or unsubstituted heteroarylamino group having 2 to 30 carbon atoms, a substituted or unsubstituted diarylamino group having 12 to 24 carbon atoms, a substituted or unsubstituted diheteroarylamino group having 2 to 24 carbon atoms, a substituted or unsubstituted aryl(heteroaryl)amino group having 7 to 24 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms, a substituted or unsubstituted alkylsilyl group having 1 to 30 carbon atoms, and a substituted or unsubstituted arylsilyl group having 6 to 30 carbon atoms.

[0037] m1 to m4 are integers from 0 to 6. When m1 to m4 are 2 or more, each of R1 to R4 is the same as or different from each other.

[0038] <3> In <1> and <2> above,

[0039] In the above [Chemical Formula A], at least one of Ar1 and Ar2 may be a phenyl group which is substituted or unsubstituted by a deuterium atom.

[0040] <4> In <1> to <3> above,

[0041] In the above [Chemical Formula A], L1 and L2 may each independently be a substituted or unsubstituted phenylene group.

[0042] <5> In <1> to <4> above,

[0043] The compound represented by [Chemical Formula A] may be substituted by at least one deuterium atom.

[0044] <6> In <5> above,

[0045] The degree of deuteration of the compound represented by [Chemical Formula A] may be 30% or more.

[0046] <7> In <1> to <6> above,

[0047] The molecular weight of the compound represented by [Chemical Formula A] can be 650 or more.

[0048] <8> Among <1> to <7> above,

[0049] The solvent may include at least one of a chlorine-based solvent, an ether-based solvent, an aromatic solvent, an aliphatic solvent, a ketone-based solvent, an ester-based solvent, an alcohol-based solvent, an amide-based solvent, and a benzoate-based solvent.

[0050] <9> Among <1> to <8> above,

[0051] The host represented by [Chemical Formula A] can be dissolved in the solvent in an amount of 1 wt% or more.

[0052] <10> Among <1> to <9> above,

[0053] The host represented by [Chemical Formula A] can be represented by any one of the following Chemical Formulas [1] to

[30] :

[0054]

[0055]

[0056]

[0057]

[0058] <11> Among <1> to <10> above,

[0059] The [Chemical Formula B-1] and [Chemical Formula B-2] may contain at least one -N(R”)2.

[0060] <12> Among <1> to <11> above,

[0061] The dopant represented by [Chemical Formula B-1] or [Chemical Formula B-2] can be represented by any one of the following [D 1] to [D 154]:

[0062]

[0063]

[0064]

[0065]

[0066]

[0067]

[0068]

[0069]

[0070] <13>Among <1> to <12>,

[0071] In addition to the light-emitting layer, the organic layer may further include at least one of a hole injection layer, a hole transport layer, a functional layer having both hole injection and hole transport functions, an electron transport layer, and an electron injection layer.

[0072] <14>Among <1> to <13>,

[0073] The organic layer may be formed by any one of spin coating, dip coating, blade coating, spray coating, roll coating, inkjet printing, and screen printing.

[0074] Effects of the Invention

[0075] The organic electroluminescent device of the present invention can be prepared using an organic electroluminescent material having high solubility in a solvent, and has excellent device operating characteristics and lifetime characteristics, such as luminous efficiency and driving voltage. Description of the Drawings

[0076] Figure 1 A schematic cross-sectional view of an organic electroluminescent device according to an example of the present invention.

[0077] Explanation of Reference Numerals

[0078] 10: Substrate

[0079] 20: First electrode

[0080] 30: Hole injection layer

[0081] 40: Hole transport layer

[0082] 50: Light-emitting layer

[0083] 60: Electron transport layer

[0084] 70: Electron injection layer

[0085] 80: Second electrode Detailed Description of the Invention

[0086] Referring to Figure 1 , an organic electroluminescent device according to an example of the present invention may include a first electrode 20, a second electrode 80 opposite to the first electrode 20, and an organic layer formed between the first electrode 20 and the second electrode 80.

[0087] For example, the first electrode 20 may be an anode, and the second electrode 80 may be a cathode. The organic layer may include a light-emitting layer 50 formed using a solution containing an organic electroluminescent material and a solvent. As needed, in addition to the light-emitting layer, the organic layer may further include at least one of a hole injection layer 30, a hole transport layer 40, a functional layer having both a hole injection function and a hole transport function, an electron transport layer 60, and an electron injection layer 70. Additionally, it may further include one or more intermediate layers.

[0088] The organic layer may be formed by a deposition process or a solution process.

[0089] For example, the deposition process may refer to a method of forming a thin film by evaporating a material substance by a method such as heating in a vacuum or low-pressure state. For example, the solution process may refer to a method of forming a solution by mixing a material substance with a solvent and then using the solution to form a thin film by methods such as spin coating, dip coating, blade coating, spraying, roll coating, inkjet printing, and screen printing.

[0090] The hole injection layer (HIL, Hole Injecting Layer) 30 may be provided between the first electrode 20 and the hole transport layer 40. For example, the hole injection layer 30 may include poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) (AI4083), [4,4',4”-tris[2-naphthyl(phenyl)amino]-triphenylamine] (2-TNATA), [N,N'-di(1-naphthyl)-N,N'-diphenylbenzidine] (NPD), [N,N'-diphenyl-N,N'-bis(3-methylphenyl)-1,1'-biphenyl-4,4'-diamine] (TPD), [N,N'-diphenyl-N,N'-bis-[4-(phenyl-m-tolyl-amino)-phenyl]-biphenyl-4,4'-diamine] (DNTPD), copper phthalocyanine, or [4,4',4”-tris(N-carbazolyl)triphenylamine] (TCTA), [4,4',4”-tris-(3-methylphenylphenylamino)triphenylamine] (m-MTDATA), etc. belonging to starburst amines, but not limited thereto, and may include substances commonly used as hole injection layers in the art.

[0091] The hole transport layer (HTL, Hole Transport Layer) 40 can be provided between the hole injection layer 30 and the light-emitting layer 50. The hole transport layer 40 can contain an electron-donating substance with a small ionization potential. More specifically, the hole transport layer 40 can mainly contain diamine, triamine, or tetraamine derivatives having a triphenylamine as a basic skeleton. For example, N,N'-bis(3-methylphenyl)-N,N'-diphenyl-[1,1'-biphenyl]-4,4'-diamine (TPD), N,N'-di(naphthalen-1-yl)-N,N'-diphenylbenzidine (α-NPD), poly[(9,9-dioctylfluorene-2,7-diyl)-co-(4,4'-(N-(4-sec-butylphenyl)diphenylamine)] (TFB), etc.

[0092] The electron transport layer (ETL, Electron Transport Layer) 60 can be provided between the second electrode 80 and the light-emitting layer 50. For example, the electron transport layer 60 can contain oxadiazole derivatives, triazine derivatives, Liq, Alq3, etc.

[0093] The electron injection layer (EIL, Electron Injecting Layer) 70 can be provided between the second electrode 80 and the electron transport layer 60. For example, the electron injection layer 70 can contain Liq, LiF, NaCl, CsF, Li2O, BaO, etc., but is not limited thereto, and can contain substances commonly used as electron injection layers in the art.

[0094] The light-emitting layer 50 can be provided between the hole transport layer 40 and the electron transport layer 60. The light-emitting layer 50 can be formed using a solution containing an organic electroluminescent material and a solvent.

[0095] The organic electroluminescent material can contain a host and a dopant. The host can contain one or more compounds represented by the following [Chemical Formula A], and the dopant can contain one or more compounds represented by the following [Chemical Formula B-1] or [Chemical Formula B-2].

[0096] [Chemical Formula A]

[0097]

[0098] In the [Chemical Formula A],

[0099] The L1 and L2 are the same as or different from each other, and each independently is selected from the group consisting of a substituted or unsubstituted alkylene having 1 to 20 carbon atoms, a substituted or unsubstituted arylene having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroarylene having 3 to 30 carbon atoms.

[0100] Each R is the same as or different from one another, and is independently selected from the group consisting of a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylthioxy group having 1 to 30 carbon atoms, a substituted or unsubstituted arylthioxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylamino group having 6 to 30 carbon atoms, a substituted or unsubstituted heteroarylamino group having 2 to 30 carbon atoms, a substituted or unsubstituted diarylamino group having 12 to 24 carbon atoms, a substituted or unsubstituted diheteroarylamino group having 2 to 24 carbon atoms, a substituted or unsubstituted aryl(heteroaryl)amino group having 7 to 24 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms, a substituted or unsubstituted alkylsilyl group having 1 to 30 carbon atoms, and a substituted or unsubstituted arylsilyl group having 6 to 30 carbon atoms.

[0101] Ar1 and Ar2 are the same as or different from one another, and are independently selected from the group consisting of a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 50 carbon atoms.

[0102] The n is an integer from 0 to 8. When n is 2 or more, each R is the same as or different from one another.

[0103] The n1 and n2 are each independently an integer from 1 to 3.

[0104] The A1 is a substituted or unsubstituted aryl group having 10 to 30 carbon atoms.

[0105]

[0106] In the [Chemical Formula B-1] and [Chemical Formula B-2],

[0107] Each of T1 to T3 is the same as or different from one another, and is independently an aromatic hydrocarbon ring having 6 to 50 carbon atoms or an aromatic heterocycle having 2 to 40 carbon atoms.

[0108] Each of T1 to T3 can be independently substituted by at least one R T When substituted by two or more Rs T These Rs Tidentical to or different from each other,

[0109] said R T is selected from any one of the group consisting of hydrogen, deuterium atom, substituted or unsubstituted alkyl having 1 to 30 carbon atoms, substituted or unsubstituted alkenyl having 2 to 30 carbon atoms, substituted or unsubstituted alkynyl having 2 to 24 carbon atoms, substituted or unsubstituted aryl having 6 to 50 carbon atoms, substituted or unsubstituted cycloalkyl having 3 to 30 carbon atoms, substituted or unsubstituted cycloalkenyl having 5 to 30 carbon atoms, substituted or unsubstituted heteroaryl having 2 to 50 carbon atoms, substituted or unsubstituted alkoxy having 1 to 30 carbon atoms, substituted or unsubstituted aryloxy having 6 to 30 carbon atoms, substituted or unsubstituted alkylthioxy having 1 to 30 carbon atoms, substituted or unsubstituted arylthioxy having 5 to 30 carbon atoms, -N(R”)2, substituted or unsubstituted alkylsilyl having 1 to 30 carbon atoms, substituted or unsubstituted arylsilyl having 5 to 30 carbon atoms, cyano and halogen,

[0110] said R”s are identical to or different from each other and are each independently selected from the group consisting of hydrogen atom, deuterium atom, substituted or unsubstituted alkyl having 1 to 30 carbon atoms, substituted or unsubstituted alkenyl having 2 to 30 carbon atoms, substituted or unsubstituted cycloalkyl having 3 to 30 carbon atoms, substituted or unsubstituted cycloalkenyl having 5 to 30 carbon atoms, substituted or unsubstituted aryl having 6 to 50 carbon atoms and substituted or unsubstituted heteroaryl having 3 to 50 carbon atoms, and said R”s can combine with each other to form an alicyclic or aromatic monocyclic or polycyclic ring,

[0111] said Y1 is selected from any one of the group consisting of N-R 11 、CR 12 R 13 、O, S and SiR 14 R 15 ;

[0112] said Y2 is selected from any one of the group consisting of N-R 16 、CR 17 R 18 、O, S and SiR 19 R 20 ;

[0113] said Y3 is selected from any one of the group consisting of N-R 21 、CR 22 R 23 、O, S and SiR 24 R 25 ;

[0114] said R 11to R 25 are the same as or different from each other, and are each independently selected from the group consisting of a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted heteroaryl group having 2 to 50 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylthioxy group having 1 to 30 carbon atoms, a substituted or unsubstituted arylthioxy group having 5 to 30 carbon atoms, a substituted or unsubstituted alkylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylamino group having 6 to 30 carbon atoms, a substituted or unsubstituted heteroarylamino group having 2 to 30 carbon atoms, a substituted or unsubstituted diarylamino group having 12 to 24 carbon atoms, a substituted or unsubstituted diheteroarylamino group having 2 to 24 carbon atoms, a substituted or unsubstituted aryl(heteroaryl)amino group having 7 to 24 carbon atoms, a substituted or unsubstituted alkylsilyl group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsilyl group having 5 to 30 carbon atoms, a cyano group, and a halogen, and the R 11 to R 25 each can combine with one or more rings selected from the group consisting of the T1 to T3 to further form an alicyclic or aromatic monocyclic or polycyclic ring.

[0115] In one example of the present invention, A1 of [Chemical Formula A] can be any one selected from the group consisting of the groups represented by the following [Chemical Formula A-1] to [Chemical Formula A-4]:

[0116]

[0117]

[0118] In the [Chemical Formula A-1] to [Chemical Formula A-4],

[0119] R1 to R4 are the same as or different from each other, and each independently is selected from the group consisting of a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylthioxy group having 1 to 30 carbon atoms, a substituted or unsubstituted arylthioxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylamino group having 6 to 30 carbon atoms, a substituted or unsubstituted heteroarylamino group having 2 to 30 carbon atoms, a substituted or unsubstituted diarylamino group having 12 to 24 carbon atoms, a substituted or unsubstituted diheteroarylamino group having 2 to 24 carbon atoms, a substituted or unsubstituted aryl(heteroaryl)amino group having 7 to 24 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms, a substituted or unsubstituted alkylsilyl group having 1 to 30 carbon atoms, and a substituted or unsubstituted arylsilyl group having 6 to 30 carbon atoms.

[0120] m1 to m4 are integers from 0 to 6, and when m1 to m4 are 2 or more, each of R1 to R4 is the same as or different from each other.

[0121] In one example of the present invention, at least one of Ar1 and Ar2 in [Chemical Formula A] can be any one of the groups represented by the following [Chemical Formula Ar-1] or [Chemical Formula Ar-2]:

[0122]

[0123]

[0124] In the [Chemical Formula Ar-1] and [Chemical Formula Ar-2],

[0125] X is selected from the group consisting of O, S, NR', and Si(R')2.

[0126] R7, R8, and R' are the same as or different from each other and are each independently selected from the group consisting of a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylthioxy group having 1 to 30 carbon atoms, a substituted or unsubstituted arylthioxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylamino group having 6 to 30 carbon atoms, a substituted or unsubstituted heteroarylamino group having 2 to 30 carbon atoms, a substituted or unsubstituted diarylamino group having 12 to 24 carbon atoms, a substituted or unsubstituted diheteroarylamino group having 2 to 24 carbon atoms, a substituted or unsubstituted aryl(heteroaryl)amino group having 7 to 24 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms, a substituted or unsubstituted alkylsilyl group having 1 to 30 carbon atoms, and a substituted or unsubstituted arylsilyl group having 6 to 30 carbon atoms.

[0127] n7 is an integer from 0 to 7, n8 is an integer from 0 to 5, and when n7 and n8 are 2 or more, each R7 and R8 are the same as or different from each other.

[0128] In one example of the present invention, Ar1 and Ar2 are each independently any one of the groups represented by [chemical formula Ar-1] or [chemical formula Ar-2], or Ar1 and Ar2 are each independently the group represented by [chemical formula Ar-1].

[0129] In one example of the present invention, X can be O or S.

[0130] In one example of the present invention, in [chemical formula A], at least one of Ar1 and Ar2 can be a phenyl group which is substituted or unsubstituted by a deuterium atom.

[0131] In one example of the present invention, L1 and L2 of [chemical formula A] can each independently be a substituted or unsubstituted phenylene group.

[0132] The "substituted" in the "substituted or unsubstituted" means being substituted by one or more substituents selected from the group consisting of a deuterium atom, a cyano group, a halogen, a hydroxyl group, a nitro group, an alkyl group having 1 to 30 carbon atoms, an alkenyl group having 2 to 30 carbon atoms, an alkynyl group having 2 to 24 carbon atoms, a cycloalkyl group having 3 to 30 carbon atoms, a cycloalkenyl group having 5 to 30 carbon atoms, a heteroalkyl group having 1 to 24 carbon atoms, an aryl group having 6 to 50 carbon atoms, an arylalkyl group having 7 to 24 carbon atoms, an alkylaryl group having 7 to 24 carbon atoms, a heteroaryl group having 2 to 50 carbon atoms, a heteroarylalkyl group having 2 to 24 carbon atoms, an alkoxy group having 1 to 30 carbon atoms, an alkylthioxy group having 1 to 30 carbon atoms, an arylthioxy group having 6 to 30 carbon atoms, -N(R")2, an alkylsilyl group having 1 to 30 carbon atoms, an arylsilyl group having 6 to 30 carbon atoms, an aryloxy group having 6 to 30 carbon atoms, and an arylsulfinyl group having 6 to 24 carbon atoms.

[0133] Moreover, considering the ranges of the alkyl or aryl groups in the "substituted or unsubstituted alkyl group having 1 to 30 carbon atoms", "substituted or unsubstituted aryl group having 6 to 50 carbon atoms", etc., the ranges of the number of carbon atoms in the alkyl group having 1 to 30 carbon atoms and the aryl group having 6 to 50 carbon atoms, etc. respectively refer to the total number of carbon atoms constituting the alkyl part or the aryl part when regarded as unsubstituted without considering the substituted part. For example, a phenyl group substituted with a para-butyl group should be regarded as corresponding to an aryl group having 6 carbon atoms substituted with a butyl group having 4 carbon atoms.

[0134] In the present specification, an aryl group refers to an aromatic system composed of a hydrocarbon containing one or more rings. When the aryl group has a substituent, it can be further fused with an adjacent substituent to form a ring.

[0135] Specific examples of the aryl group include phenyl, o-biphenyl, m-biphenyl, p-biphenyl, o-terphenyl, m-terphenyl, p-terphenyl, naphthyl, anthracenyl, phenanthrenyl, pyrenyl, indenyl, fluorenyl, tetrahydronaphthyl, perylenyl, anthryl, tetracenyl, fluoranthenyl, benzophenanthrenyl and other aromatic groups.

[0136] In the present specification, a heteroaryl group refers to a cyclic aromatic system having 2 to 24 carbon atoms containing 1, 2 or 3 heteroatoms selected from N, O, P, Si, S, Ge, Se or Te and the remaining ring atoms being carbon, and these rings can be fused to form a ring. Moreover, one or more hydrogen atoms in the heteroaryl group can be substituted with the same substituents as in the case of the aryl group.

[0137] As specific examples of the heteroaryl group, furyl, benzofuryl, dibenzofuryl, thienyl, benzothienyl, dibenzothienyl, pyrrolyl, indolyl, carbazolyl, pyridyl, quinolinyl, imidazolyl, benzimidazolyl, oxazolyl, benzoxazolyl, triazinyl, triazolyl, piperidinyl, acridinyl, phenoxazinyl, thiazolyl, benzothiazolyl, pyrimidinyl, pyrazinyl, etc. can be cited.

[0138] In the present specification, the alkyl group is linear or branched, and as specific examples thereof, methyl, ethyl, propyl, isopropyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, hexyl, etc. can be cited, and one or more hydrogen atoms in the alkyl group can be substituted with the same substituents as in the case of the aryl group.

[0139] In the present specification, the heteroalkyl group means that one or more carbon atoms in the main chain of the alkyl group, preferably 1 to 5 carbon atoms, are substituted with heteroatoms such as oxygen atom, sulfur atom, nitrogen atom, phosphorus atom, etc. And one or more hydrogen atoms in the heteroalkyl group can be substituted with the same substituents as in the case of the alkyl group.

[0140] In the present specification, the "ring" in the cycloalkyl group means a substituent having a structure capable of forming a saturated hydrocarbon monocyclic or polycyclic ring in the alkyl group. As specific examples of the cycloalkyl group, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, methylcyclopentyl, methylcyclohexyl, ethylcyclopentyl, ethylcyclohexyl, adamantyl, bicyclophenyl dienyl, decahydronaphthyl, norbornyl, borneol, isoborneol, etc. can be cited, and one or more hydrogen atoms in the cycloalkyl group can be substituted with the same substituents as in the case of the aryl group.

[0141] In the present specification, the alkoxy group is a substituent in which an oxygen atom is bonded to the end of an alkyl group or a cycloalkyl group. As specific examples thereof, methoxy, ethoxy, propoxy, isobutoxy, sec-butoxy, pentyloxy, isopentyloxy, hexyloxy, etc. can be cited, and one or more hydrogen atoms in the alkoxy group can be substituted with the same substituents as in the case of the aryl group.

[0142] In the present specification, as specific examples of the arylalkyl group, benzyl, phenethyl, phenylpropyl, naphthylmethyl, naphthylethyl, etc. can be cited, and one or more hydrogen atoms in the arylalkyl group can be substituted with the same substituents as in the case of the aryl group.

[0143] In the present specification, as specific examples of the alkylsilyl group, trimethylsilyl, triethylsilyl, methylcyclobutylsilyl, etc. can be cited, and one or more hydrogen atoms in the alkylsilyl group can be substituted with the same substituents as in the case of the aryl group.

[0144] In this specification, specific examples of the arylsilyl group include triphenylsilyl, diphenylmethylsilyl, diphenylethenylsilyl, etc., and one or more hydrogen atoms in the arylsilyl group may be substituted with the same substituents as in the case of the aryl group.

[0145] In this specification, an alkenyl group means an alkyl substituent containing one carbon-carbon double bond formed by two carbon atoms, and an alkynyl group means an alkyl substituent containing one carbon-carbon triple bond formed by two carbon atoms.

[0146] In this specification, a diarylamino group means an amino group in which two identical or different aryl groups as described above are bonded to a nitrogen atom, and a diheteroarylamino group of the compound of the present invention means an amino group in which two identical or different heteroaryl groups are bonded to a nitrogen atom. Further, the aryl(heteroaryl)amino group means an amino group in which the aryl group and the heteroaryl group are respectively bonded to a nitrogen atom.

[0147] In one example of the present invention, the compound represented by [Chemical Formula A] may be substituted with at least one deuterium atom. When the compound represented by [Chemical Formula A] is substituted with at least one deuterium atom, the solubility of the compound represented by [Chemical Formula A] in a solvent can be increased. Preferably, the degree of deuteration of the compound represented by [Chemical Formula A] can be 15% or more, more preferably, it can be 30% or more, 40% or more, or 50% or more.

[0148] When the compound represented by [Chemical Formula A] is substituted with a deuterium atom, the ground state energy is lowered compared to a C-H bond, and as the bond force increases, the heat resistance is further improved and the lifespan can be increased.

[0149] In one example of the present invention, the molecular weight of the compound represented by [Chemical Formula A] can be 650 or more, preferably, it can be 700 or more, more preferably, it can be 750 or more, and further preferably, it can be 800 or more.

[0150] The lower the molecular weight of the compound represented by [Chemical Formula A], the more likely it is to cause the phenomenon of contaminating adjacent pixels, i.e., the interference effect, in the inkjet process. The higher the molecular weight of the compound represented by [Chemical Formula A], the higher its solubility in a solvent.

[0151] In one example of the present invention, the preferred compound of the host may be any one selected from the compounds represented by Chemical Formulas [1] to

[30] .

[0152] In the chemical formula, the subscripts of D4, D5, D6, and D8 respectively represent the number of substituted deuterium atoms.

[0153] As the host, one compound may be used, or two or more compounds may be used together.

[0154] The solubility of the host in the solvent can be 0.1 wt% or more and 50 wt% or less, 0.5 wt% or more and 20 wt% or less, preferably 1 wt% or more, and more preferably 2 wt% or more.

[0155] The solvent may include at least one of a chlorine-based solvent, an ether-based solvent, an aromatic solvent, an aliphatic solvent, a ketone-based solvent, an ester-based solvent, an alcohol-based solvent, an amide-based solvent, and a benzoate-based solvent. The solvent may be a single pure substance or a mixture, and preferably, it may be a benzoate-based solvent.

[0156] For example, the chlorine-based solvent may include chloroform, dichloromethane, or chlorobenzene, the ether-based solvent may include tetrahydrofuran or dioxane, the aromatic solvent may include toluene, xylene, or mesitylene, the aliphatic solvent may include cyclohexane, n-pentane, or n-hexane, the ketone-based solvent may include acetone, methyl ethyl ketone, or cyclohexanone, the ester-based solvent may include ethyl acetate or butyl acetate, the alcohol-based solvent may include methanol, ethanol, propanol, or cyclohexanol, the amide-based solvent may include N,N-dimethylformamide, and the benzoate-based solvent may include methyl benzoate, ethyl benzoate, or butyl benzoate.

[0157] The solvent may be used alone, or two or more solvents may be mixed and used.

[0158] The boiling point of the solvent may be 60°C to 300°C, preferably 130°C to 300°C, but is not limited thereto.

[0159] The viscosity of the solvent may be 1 cP to 10 cP, preferably 2 cP to 8 cP, but is not limited thereto.

[0160] In one example of the present invention, [Chemical Formula B-1] and [Chemical Formula B-2] may contain at least one -N(R”)2.

[0161] In one example of the present invention, the dopant represented by [Chemical Formula B-1] or [Chemical Formula B-2] may be any one selected from the compounds represented by the chemical formulas [D 1] to [D 154].

[0162] Based on 100 parts by weight of the host, the amount of the dopant represented by [Chemical Formula B-1] or [Chemical Formula B-2] may be 0.01 parts by weight to 20 parts by weight.

[0163] A solution containing the compound represented by [Chemical Formula A], the compound represented by [Chemical Formula B-1] or [Chemical Formula B-2], and a solvent is suitable for manufacturing an organic electroluminescent device using a solution process.

[0164] The solution may further contain a fluorescent dopant or a phosphorescent dopant.

[0165] For example, the fluorescent dopant may include pyrene compounds, deuterium-substituted pyrene compounds, arylamines, deuterium-substituted arylamines, perylene compounds, deuterium-substituted perylene compounds, pyrrole compounds, deuterium-substituted pyrrole compounds, boron compounds, fluorene compounds, deuterium-substituted fluorene compounds, hydrazone compounds, deuterium-substituted hydrazone compounds, carbazole compounds, deuterium-substituted carbazole compounds, stilbene compounds, deuterium-substituted stilbene compounds, starburst compounds, deuterium-substituted starburst compounds, oxadiazole compounds, deuterium-substituted oxadiazole compounds, coumarine, deuterium-substituted coumarine, but not limited thereto.

[0166] As the phosphorescent dopant, an organometallic compound containing iridium, platinum, osmium, titanium, zirconium, hafnium, europium, terbium, thulium, iron, cobalt, nickel, ruthenium, rhodium, palladium or a combination thereof can be cited, but not limited thereto.

[0167] Based on 100 parts by weight of the host, the amount of the fluorescent dopant or the phosphorescent dopant may be 0.01 part by weight to 20 parts by weight.

[0168] The content of the organic electroluminescent material containing the compound represented by [Chemical Formula A] in the solution may be 0.5 wt% or more, preferably 1.0 wt% or more, more preferably 2.0 wt% or more, but not limited thereto.

[0169] Next, with reference to Figure 1 A method for manufacturing an organic electroluminescent device according to an embodiment of the present invention will be described.

[0170] A substrate 10 may be prepared. The substrate 10 may be an organic substrate or a transparent plastic substrate having excellent transparency, surface smoothness, handleability and waterproofness, but not limited thereto, and may include substrates commonly used for organic electroluminescent devices.

[0171] A first electrode 20 may be formed by coating a material for an anode electrode on the upper surface of the substrate 10. The material for the anode electrode may include a material that is transparent and has excellent conductivity, for example, indium tin oxide (ITO), indium zinc oxide (IZO), tin oxide (SnO2) and / or zinc oxide (ZnO).

[0172] A hole injection layer 30 may be formed by vacuum thermal deposition or spin coating of a hole injection layer material on the upper surface of the first electrode 20. A hole transport layer 40 may be formed by vacuum thermal deposition or spin coating of a hole transport layer material on the upper surface of the hole injection layer 30.

[0173] An electron blocking layer (not shown) can be formed by selectively vacuum thermally depositing or spin-coating an electron blocking layer material on the upper surface of the hole transport layer 40. The electron blocking layer prevents electrons injected from the electron injection layer 70 from passing through the light-emitting layer 50 and entering the hole transport layer 40, thereby improving the device lifetime and efficiency. The electron blocking layer can be formed at an appropriate portion between the light-emitting layer 50 and the hole injection layer 30, and preferably, can be formed between the light-emitting layer 50 and the hole transport layer 40.

[0174] The light-emitting layer 50 can be formed on the upper surface of the hole transport layer 40 or the electron blocking layer. The light-emitting layer 50 can be formed using a solution containing the organic electroluminescent material and the solvent. More specifically, the light-emitting layer 50 can be formed by coating the solution on the upper surface of the hole transport layer 40 by any one of spin coating, dip coating, blade coating, spraying, roll coating, inkjet printing, and screen printing.

[0175] In an example of the present invention, the thickness of the light-emitting layer 50 can be to

[0176] A hole blocking layer (not shown) can be selectively formed on the upper surface of the light-emitting layer 50 by vacuum deposition or spin coating. Since the lifetime and efficiency of the organic electroluminescent device decrease when holes pass through the light-emitting layer 50 and flow into the second electrode 80, if the hole blocking layer contains a hole blocking material having a very low highest occupied molecular orbital (HOMO) energy level, holes can be prevented from passing through the light-emitting layer 50 and flowing into the second electrode 80. The hole blocking material is not particularly limited, but can have electron transport ability and a higher ionization potential than the organic electroluminescent material. The hole blocking material can include, for example, BAlq, BCP, TPBI, etc.

[0177] The electron injection layer 70 can be formed by vacuum depositing or spin coating the electron transport layer 60 on the upper surface of the light-emitting layer 50 or the hole blocking layer, and the second electrode 80 can be formed by vacuum thermally depositing a cathode electrode metal on the upper surface of the electron injection layer 70. The cathode electrode metal can include, for example, lithium (Li), magnesium (Mg), aluminum (Al), aluminum-lithium (Al-Li), calcium (Ca), magnesium-indium (Mg-In), magnesium-silver (Mg-Ag), etc. When manufacturing a top-emitting organic electroluminescent device, the cathode electrode metal can include indium tin oxide (ITO) or indium zinc oxide (IZO).

[0178] An organic electroluminescent device according to an example of the present invention can be manufactured by the manufacturing method described above.

[0179] Hereinafter, the organic electroluminescent device of the present invention will be described with reference to preferred embodiments. However, these embodiments are for more detailed illustration of the present invention, and it is obvious to those skilled in the art that the scope of the present invention is not limited thereto.

[0180] Synthesis Example 1: Synthesis of [1]

[0181] Synthesis Example 1-(1): Synthesis of Intermediate 1-a

[0182]

[0183] 1-Bromo-3-iodobenzene (13.0 g, 0.046 mol), B-[10-(phenyl-2,3,4,5,6-d5)-9-anthryl]boronic acid (14.5 g, 0.048 mol), Pd(PPh3)4 (0.9 g, 0.001 mol), and potassium carbonate (11.1 g, 0.08 mol) were added to a 2 L round-bottom flask, and then 100 mL of toluene, 45 mL of ethanol, and 30 mL of water were added. The reactor was refluxed and stirred overnight. After the reaction was completed, the temperature of the reactor was lowered to room temperature, and extraction was performed with ethyl acetate. After the organic layer was concentrated under reduced pressure, separation was carried out by column chromatography. The solid was recrystallized with heptane to obtain <Intermediate 1-a> (12.4 g, 65%).

[0184] Synthesis Example 1-(2): Synthesis of Intermediate 1-b

[0185]

[0186] <Intermediate 1-a> (19.0 g, 0.046 mol) and 145.6 mL of tetrahydrofuran were added to a 1 L flask, and the inside of the reactor was cooled to -78 °C under a nitrogen atmosphere and stirred. Butyllithium (1.6 M) (32 mL) was added dropwise, and the mixture was stirred at the same temperature for 1 hour. Trimethyl borate (8 mL) was added dropwise, and the reaction solution was stirred at room temperature for 2 hours. After the reaction was completed, it was poured into a 2 M hydrochloric acid aqueous solution (100 mL) and stirred, extracted with ethyl acetate (50 mL), concentrated under reduced pressure, and then poured into an excess of heptane to filter the resulting solid to obtain <Intermediate 1-b> (12.9 g, 74%).

[0187] Synthesis Example 1-(3): Synthesis of Intermediate 1-c

[0188]

[0189] <Intermediate 1-c> was synthesized in the same manner except that 1-bromo-4-iodobenzene was used instead of 1-bromo-3-iodobenzene used in Synthesis Example 1-(1). (Yield: 67%)

[0190] Synthesis Example 1-(4): Synthesis of Intermediate 1-d

[0191]

[0192] <Intermediate 1-d> was synthesized in the same manner except that <Intermediate 1-c> was used instead of <Intermediate 1-a> used in Synthesis Example 1-(2). (Yield: 72%)

[0193] Synthesis Example 1-(5): Synthesis of Intermediate 1-e

[0194]

[0195] <Intermediate 1-e> was synthesized in the same manner except that 2-bromo-1-iodonaphthalene was used instead of 1-bromo-3-iodobenzene used in Synthesis Example 1-(1), and <Intermediate 1-d> was used instead of B-[10-(phenyl-2,3,4,5,6-d5)-9-anthryl]boronic acid. (Yield: 66%)

[0196] Synthesis Example 1-(6): Synthesis of [1]

[0197]

[0198] <Intermediate 1-b> (28.8 g, 0.076 mol), <Intermediate 1-e> (42.7 g, 0.079 mol), tetrakis(triphenylphosphine)palladium (1.7 g, 0.001 mol), and potassium carbonate (20.09 g, 0.145 mol) were added to a 500 mL flask, and then 125 mL of toluene, 125 mL of ethanol, and 50 mL of water were added. The inside of the reactor was refluxed under a nitrogen atmosphere. After the reaction was completed, the reaction mixture was poured into an excess of methanol, and the resulting solid was filtered. The filtered solid was further filtered to obtain [1] (48.3 g, 80%).

[0199] MS (MALDI-TOF): m / z 794.38 [M +

[0200] Synthesis Example 2: Synthesis of [8]

[0201] Synthesis Example 2-(1): Synthesis of Intermediate 2-a

[0202]

[0203] ​Except for using 2-bromo-3-iodonaphthalene in place of 2-bromo-1-iodonaphthalene used in Synthesis Example 1-(5), it was synthesized in the same manner to obtain <Intermediate 2-a>. (Yield: 63%)

[0204] Synthesis Example 2-(2): Synthesis of [8]

[0205]

[0206] Except for using <Intermediate 2-a> in place of <Intermediate 1-e> used in Synthesis Example 1-(6), it was synthesized in the same manner to obtain [8]. (Yield: 77%)

[0207] MS(MALDI-TOF): m / z 794.38 [M +

[0208] Synthesis Example 3: Synthesis of

[11]

[0209] Synthesis Example 3-(1): Synthesis of Intermediate 3-a

[0210]

[0211] Except for using 9-bromo-10-(1-naphthalenyl-2,3,4,5,6,7,8-d7)anthracene-1,2,3,4,5,6,7,8,9-d8 in place of <Intermediate 1-a> used in Synthesis Example 1-(2), it was synthesized in the same manner to obtain <Intermediate 3-a>. (Yield: 75%)

[0212] Synthesis Example 3-(2): Synthesis of Intermediate 3-b

[0213]

[0214] Except for using <Intermediate 3-a> in place of B-[10-(phenyl-2,3,4,5,6-d5)-9-anthracenyl]boronic acid used in Synthesis Example 1-(1), it was synthesized in the same manner to obtain <Intermediate 3-b>.

[0215] (Yield: 66%)

[0216] Synthesis Example 3-(3): Synthesis of Intermediate 3-c

[0217]

[0218] Except for using <Intermediate 3-b> in place of <Intermediate 1-a> used in Synthesis Example 1-(2), it was synthesized in the same manner to obtain <Intermediate 3-c>. (Yield: 74%)

[0219] Synthesis Example 3-(4): Synthesis of Intermediate 3-d​

[0220]

[0221] Except for using 1-bromo-8-iodonaphthalene in place of 1-bromo-3-iodobenzene used in Synthesis Example 1-(1) and using <Intermediate 3-c> in place of B-[10-(phenyl-2,3,4,5,6-d5)-9-anthryl]boronic acid, it was synthesized in the same manner to obtain <Intermediate 3-d>. (Yield: 64%)

[0222] Synthesis Example 3-(5): Synthesis of

[11]

[0223]

[0224] Except for using <Intermediate 3-d> in place of <Intermediate 1-e> used in Synthesis Example 1-(6), it was synthesized in the same manner to obtain

[11] . (Yield: 75%)

[0225] MS (MALDI-TOF): m / z 846.40 [M +

[0226] Synthesis Example 4: Synthesis of

[18]

[0227] Synthesis Example 4-(1): Synthesis of Intermediate 4-a

[0228]

[0229] Except for using B-[10-(phenyl-2,3,4,5,6-d5)-9-anthryl-1,2,3,4,5,6,7,8-d8]-boronic acid in place of B-[10-(phenyl-2,3,4,5,6-d5)-9-anthryl]boronic acid used in Synthesis Example 1-(1), it was synthesized in the same manner to obtain <Intermediate 4-a>. (Yield: 64%)

[0230] Synthesis Example 4-(2): Synthesis of Intermediate 4-b

[0231]

[0232] Except for using <Intermediate 4-a> in place of <Intermediate 1-a> used in Synthesis Example 1-(2), it was synthesized in the same manner to obtain <Intermediate 4-b>. (Yield: 75%)

[0233] Synthesis Example 4-(3): Synthesis of Intermediate 4-c

[0234]

[0235] ​Except for using 2-bromo-7-iodonaphthalene in place of 2-bromo-1-iodonaphthalene used in Synthesis Example 1-(5), and using <Intermediate 4-b> in place of <Intermediate 1-d>, it was synthesized in the same manner to obtain <Intermediate 4-c>. (Yield: 70%)

[0236] Synthesis Example 4-(4): Synthesis of Intermediate 4-d

[0237]

[0238] Except for using 1-bromo-4-iodobenzene in place of 1-bromo-3-iodobenzene used in Synthesis Example 4-(1), it was synthesized in the same manner to obtain <Intermediate 4-d>. (Yield: 68%)

[0239] Synthesis Example 4-(5): Synthesis of Intermediate 4-e

[0240]

[0241] Except for using <Intermediate 4-d> in place of <Intermediate 1-a> used in Synthesis Example 1-(2), it was synthesized in the same manner to obtain <Intermediate 4-e>. (Yield: 75%)

[0242] Synthesis Example 4-(6): Synthesis of

[18]

[0243]

[0244] Except for using <Intermediate 4-e> in place of <Intermediate 1-b> used in Synthesis Example 1-(6), and using <Intermediate 4-c> in place of <Intermediate 1-e>, it was synthesized in the same manner to obtain

[18] . (Yield: 82%)

[0245] MS(MALDI-TOF): m / z 810.48 [M +

[0246] Synthesis Example 5: Synthesis of [D12]

[0247] Synthesis Example 5-(1): Synthesis of Intermediate 5-a

[0248]

[0249]

[0250] ​Add 1-bromo-2,3-dichloro-5-(1,1-dimethylethyl)benzene (21.7 g, 0.077 mol), 4-isopropylaniline (11.4 g, 0.084 mol), 1.42 g of tris(dibenzylideneacetone)dipalladium(0), 0.96 g of bis(diphenylphosphine)-1,1'-binaphthyl, 14.9 g of sodium tert-butoxide, and 375 mL of toluene to the reactor, reflux and stir for 3 hours. After cooling to room temperature, add ethyl acetate and water, and separate the organic layer. Purify by silica gel chromatography to obtain <Intermediate 5-a>. (20.7 g, 80%)

[0251] Synthesis Example 5-(2): Synthesis of Intermediate 5-b

[0252]

[0253] In a 250 mL reactor, add <Intermediate 5-a> (33.0 g, 0.098 mol), 3-bromo-5-(1,1-dimethylethyl)benzofuran (24.8 g, 0.098 mol), palladium acetate (0.5 g, 0.002 mol), sodium tert-butoxide (18.9 g, 0.196 mol), tri-tert-butylphosphine (0.8 g, 0.004 mol), and 200 mL of toluene, reflux and stir for 5 hours. After the reaction is completed, filter, concentrate the filtrate, and separate by column chromatography to obtain <Intermediate 5-b> (38.9 g, 78%).

[0254] Synthesis Example 5-(3): Synthesis of Intermediate 5-c

[0255]

[0256] 1-Bromo-3-tert-butylbenzene (27.7 g, 0.13 mol), 4-isopropylaniline (18.9 g, 0.14 mol), 2.3 g of tris(dibenzylideneacetone)dipalladium(0), 24.2 g of sodium tert-butoxide, 1.5 g of bis(diphenylphosphine)-1,1'-binaphthyl, and 550 mL of toluene were added to the reactor, and then refluxed and stirred for 6 hours. After cooling to room temperature, ethyl acetate and water were added, and the organic layer was separated. Purification by silica gel chromatography gave <Intermediate 5-c> (29.2 g, 84%).

[0257] Synthesis Example 5-(4): Synthesis of Intermediate 5-d

[0258]

[0259] In a reactor, <Intermediate 5-b> (20.3 g, 0.04 mol), <Intermediate 5-c> (10.7 g, 0.04 mol), 0.6 g of bis(tri-tert-butylphosphine)palladium(0), 5.8 g of sodium tert-butoxide, and 350 mL of toluene were added, and the mixture was refluxed and stirred for 6 hours. After cooling to room temperature, ethyl acetate and water were added, and the organic layer was separated. Purification by silica gel chromatography gave <Intermediate 5-d> (28.1 g, 95%).

[0260] Synthesis Example 5-(5): Synthesis of [D12]

[0261]

[0262] In a reactor, <Intermediate 5-d> (22.2 g, 0.03 mol) and 420 mL of tert-butylbenzene were added. A 51 mL solution of 1.7 M tert-butyllithium in pentane was added dropwise at -78 °C. After warming to 60 °C, the mixture was stirred for 2 hours, and then nitrogen was bubbled through at 60 °C to completely remove pentane. After cooling to -78 °C, 14.5 mL of boron tribromide was added dropwise. After warming to room temperature, the mixture was stirred for 2 hours, then cooled to 0 °C, and 7.5 mL of N,N-diisopropylethylamine was added dropwise. After warming to 120 °C, the mixture was stirred for 16 hours. After cooling to room temperature, 10% aqueous sodium acetate solution and ethyl acetate were added, and then the organic layer was separated and concentrated under reduced pressure. Purification by silica gel chromatography gave [D 12] (3.2 g, 15%).

[0263] MS (MALDI-TOF): m / z 712.46 [M +

[0264] Synthesis Example 6: Synthesis of [D54]

[0265] Synthesis Example 6-(1): Synthesis of Intermediate 6-a

[0266]

[0267] Except for using 1-bromo-2,3-dichloro-5-methylbenzene instead of 1-bromo-2,3-dichloro-5-(1,1-dimethylethyl)benzene used in Synthesis Example 5-(1) and using 4'-(1,1-dimethylethyl)[1,1'-biphenyl]-3-amine instead of 4-isopropylaniline, it was synthesized in the same manner to obtain <Intermediate 6-a>. (Yield: 76%)

[0268] Synthesis Example 6-(2): Synthesis of Intermediate 6-b

[0269]

[0270] ​Except for using <Intermediate 6-a> instead of <Intermediate 5-a> used in Synthesis Example 5-(2) and using 3-bromobenzothiophene instead of 3-bromo-5-(1,1-dimethylethyl)benzofuran, it was synthesized in the same manner to obtain <Intermediate 6-b>. (Yield: 75%)

[0271] Synthesis Example 6-(3): Synthesis of Intermediate 6-c

[0272]

[0273] Except for using 3-bromo-4'-(1,1-dimethylethyl)-1,1'-biphenyl instead of 1-bromo-3-tert-butylbenzene used in Synthesis Example 5-(3) and using aniline instead of 4-isopropyl aniline, it was synthesized in the same manner to obtain <Intermediate 6-c>. (Yield: 80%)

[0274] Synthesis Example 6-(4): Synthesis of Intermediate 6-d

[0275]

[0276] Except for using <Intermediate 6-b> instead of <Intermediate 5-b> used in Synthesis Example 5-(4) and using <Intermediate 6-c> instead of <Intermediate 5-c>, it was synthesized in the same manner to obtain <Intermediate 6-d>. (Yield: 92%)

[0277] Synthesis Example 6-(5): Synthesis of [D54]

[0278]

[0279] Except for using <Intermediate 6-d> instead of <Intermediate 5-d> used in Synthesis Example 5-(5), it was synthesized in the same manner to obtain [D 54]. (Yield: 20%)

[0280] MS(MALDI-TOF): m / z 804.46[M +

[0281] Synthesis Example 7: Synthesis of [D80]

[0282] Synthesis Example 7-(1): Synthesis of Intermediate 7-a

[0283]

[0284] ​3-Bromo-N,N-bis[4-(1,1-dimethylethyl)phenyl]aniline (56.7 g, 0.13 mol), aniline (13.0 g, 0.14 mol), 2.3 g of tris(dibenzylideneacetone)dipalladium(0), 24.2 g of sodium tert-butoxide, 1.5 g of bis(diphenylphosphino)-1,1'-binaphthalene, and 550 mL were added to a reactor, and the mixture was refluxed and stirred for 6 hours. After cooling to room temperature, ethyl acetate and water were added, and the organic layer was separated. Purification by silica gel chromatography gave <Intermediate 7-a> (49.0 g, 84%).

[0285] Synthesis Example 7-(2): Synthesis of Intermediate 7-b

[0286]

[0287] Except for using <Intermediate 7-a> instead of <Intermediate 6-c> used in Synthesis Example 6-(4), it was synthesized in the same manner to obtain <Intermediate 7-b>. (Yield: 90%)

[0288] Synthesis Example 7-(3): Synthesis of Intermediate [D80]

[0289]

[0290] Except for using <Intermediate 7-b> instead of <Intermediate 5-d> used in Synthesis Example 5-(5), it was synthesized in the same manner to obtain [D80]. (Yield: 18%)

[0291] MS (MALDI-TOF): m / z 901.46 [M +

[0292] Examples 1 to 12

[0293] ​Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) (AI4083), which is widely used as a hole injection layer, was spin-coated on the ITO transparent electrode to form a film with a thickness of 60 nm, and then baked at 200 °C for 30 minutes to form a hole injection layer. TFB was spin-coated on the hole injection layer to form a film with a thickness of 20 nm, and then baked at 130 °C for 10 minutes to form a hole transport layer. A 2 wt% solution of methyl benzoate containing the host compound and dopant of the present invention shown in Table 1 below (weight ratio of host:dopant: 97:3) was spin-coated on the hole transport layer to form a film with a thickness of 30 nm, and then baked at 180 °C for 30 minutes to form a light-emitting layer. It was baked at 130 °C for 10 minutes in a nitrogen atmosphere, and then [E-1] and [E-2] were deposited in a ratio of 1:1 as an electron transport layer to form a film with a thickness of 25 nm. [E-2] was deposited as an electron injection layer on the electron transport layer to form a film with a thickness of 1 nm. Finally, aluminum was deposited as a cathode on the electron injection layer with a thickness of 100 nm to fabricate an organic light-emitting device. The luminescence characteristics of the organic light-emitting device were measured at 10 mA / cm 2 The luminescence characteristics of the organic light-emitting device were measured at 10 mA / cm

[0294] Comparative Examples 1 to 14

[0295] Except that [BH1] and [BH2] were used instead of the compound of the present invention as the host or [RBD-1] and [RBD-2] were used instead of the compound of the present invention as the dopant in the device structure of the above embodiments, the organic light-emitting devices of the comparative examples were fabricated in the same manner, and the luminescence characteristics of the organic light-emitting devices were measured at 10 mA / cm 2 The luminescence characteristics of the organic light-emitting device were measured at 10 mA / cm

[0296]

[0297]

[0298] Table 1

[0299]

[0300]

[0301] The voltage, efficiency, and lifetime of the organic electroluminescent devices fabricated according to Examples 1 to 12 and Comparative Examples 1 to 14 were measured, and the results are shown in Table 1. Among them, T95 refers to the time required for the luminance to decrease to 95% of the initial luminance.

[0302] It was confirmed that the devices of the examples using the compound of the present invention exhibited good driving voltage and efficiency, and the lifetime characteristics were improved compared with the devices of the comparative examples.

Claims

1. An organic electroluminescent device, comprising: a first electrode; a second electrode; and an organic layer formed between the first electrode and the second electrode, wherein the organic electroluminescent device is characterized in that: The organic layer includes a light-emitting layer formed using a solution containing an organic electroluminescent material and a solvent, The organic electroluminescent material comprises a host and a dopant, The host includes one or more compounds represented by the following [Chemical Formula A], and the dopant includes one or more compounds represented by the following [Chemical Formula B-1] or [Chemical Formula B-2]: [Chemical formula A] In the [Chemical Formula A], The L1 and L2 are the same as or different from each other and are independently selected from the group consisting of a substituted or unsubstituted alkylene group having 1 to 20 carbon atoms, a substituted or unsubstituted arylene group having 6 to 30 carbon atoms, and a substituted or unsubstituted heteroarylene group having 3 to 30 carbon atoms. The R's are the same as or different from each other and are each independently selected from a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylthiooxy group having 1 to 30 carbon atoms, a substituted or unsubstituted arylthiooxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylthiooxy group having 1 to 30 carbon atoms, The group consisting of an alkylamino group, a substituted or unsubstituted arylamino group having 6 to 30 carbon atoms, a substituted or unsubstituted heteroarylamino group having 2 to 30 carbon atoms, a substituted or unsubstituted diarylamino group having 12 to 24 carbon atoms, a substituted or unsubstituted diheteroarylamino group having 2 to 24 carbon atoms, a substituted or unsubstituted aryl (heteroaryl)amino group having 7 to 24 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms, a substituted or unsubstituted alkylsilyl group having 1 to 30 carbon atoms and a substituted or unsubstituted arylsilyl group having 6 to 30 carbon atoms, Ar1 and Ar2 are the same as or different from each other and are each independently selected from the group consisting of a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, The n is an integer from 0 to 8. When n is 2 or more, each R is the same or different from each other. The n1 and n2 are each independently an integer from 1 to 3, A1 is a substituted or unsubstituted aromatic group having 10 to 30 carbon atoms, In the above [Chemical Formula B-1] and [Chemical Formula B-2], The T1 to T3 are the same as or different from each other, and are independently an aromatic hydrocarbon ring having 6 to 50 carbon atoms, or an aromatic heterocyclic ring having 2 to 40 carbon atoms, The T1 to T3 can each be independently represented by at least one R T Replaced by two or more R T When replaced, these R T Same or different from each other, The R T The alkyl radical is selected from hydrogen, a deuterium atom, a substituted or unsubstituted alkyl radical having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl radical having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl radical having 2 to 24 carbon atoms, a substituted or unsubstituted aryl radical having 6 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl radical having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl radical having 5 to 30 carbon atoms, a substituted or unsubstituted heteroaryl radical having 2 to 50 carbon atoms, a substituted or any one of the group consisting of an unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylthiooxy group having 1 to 30 carbon atoms, a substituted or unsubstituted arylthiooxy group having 5 to 30 carbon atoms, -N(R")2, a substituted or unsubstituted alkylsilyl group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsilyl group having 5 to 30 carbon atoms, a cyano group and a halogen group, The R" are the same as or different from each other, and are independently selected from the group consisting of a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms, and the R" can be combined with each other to form an alicyclic or aromatic monocyclic or polycyclic ring, The Y1 is selected from NR 11 , CR 12 R 13 , O, S and SiR 14 R 15 Any of the groups consisting of The Y2 is selected from NR 16 , CR 17 R 18 , O, S and SiR 19 R 20 Any of the groups consisting of The Y3 is selected from NR 21 , CR 22 R 23 , O, S and SiR 24 R 25 Any of the groups consisting of The R 11 To R 25 Each of them is the same as or different from each other and is independently selected from a hydrogen atom, a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted heteroaryl group having 2 to 50 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms any one of the group consisting of thioxy, substituted or unsubstituted arylthioxy having 5 to 30 carbon atoms, substituted or unsubstituted alkylamino having 1 to 30 carbon atoms, substituted or unsubstituted arylamino having 6 to 30 carbon atoms, substituted or unsubstituted heteroarylamino having 2 to 30 carbon atoms, substituted or unsubstituted diarylamino having 12 to 24 carbon atoms, substituted or unsubstituted diheteroarylamino having 2 to 24 carbon atoms, substituted or unsubstituted aryl (heteroaryl)amino having 7 to 24 carbon atoms, substituted or unsubstituted alkylsilyl having 1 to 30 carbon atoms, substituted or unsubstituted arylsilyl having 5 to 30 carbon atoms, cyano and halogen, wherein R 11 To R 25 Each of them can be combined with one or more rings selected from the group consisting of T1 to T3 to further form an alicyclic or aromatic monocyclic or polycyclic ring.

2. The organic electroluminescent device according to claim 1, characterized in that: In the above [Chemical Formula A], A1 is any one selected from the group consisting of groups represented by the following [Chemical Formula A-1] to [Chemical Formula A-4]: In the above [Chemical Formula A-1] to [Chemical Formula A-4], R1 to R4 are the same as or different from each other and are each independently selected from a deuterium atom, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkylthiooxy group having 1 to 30 carbon atoms, a substituted or unsubstituted arylthiooxy group having 6 to 30 carbon atoms, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, The group consisting of an amino group, a substituted or unsubstituted arylamino group having 6 to 30 carbon atoms, a substituted or unsubstituted heteroarylamino group having 2 to 30 carbon atoms, a substituted or unsubstituted diarylamino group having 12 to 24 carbon atoms, a substituted or unsubstituted diheteroarylamino group having 2 to 24 carbon atoms, a substituted or unsubstituted aryl (heteroaryl)amino group having 7 to 24 carbon atoms, a substituted or unsubstituted aryl group having 6 to 50 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms, a substituted or unsubstituted alkylsilyl group having 1 to 30 carbon atoms, and a substituted or unsubstituted arylsilyl group having 6 to 30 carbon atoms, The m1 to m4 are integers of 0 to 6. When m1 to m4 are 2 or more, each of R1 to R4 is the same as or different from each other.

3. The organic electroluminescent device according to claim 1, characterized in that: In the above [Chemical Formula A], at least one of Ar1 and Ar2 is a phenyl group which may be substituted by a deuterium atom.

4. The organic electroluminescent device according to claim 1, characterized in that: In the [Chemical Formula A], L1 and L2 are each independently a substituted or unsubstituted phenylene group.

5. The organic electroluminescent device according to claim 1, characterized in that: The compound represented by [Chemical Formula A] is substituted with at least one deuterium atom.

6. The organic electroluminescent device according to claim 5, characterized in that: The degree of deuteration of the compound represented by [Chemical Formula A] is 30% or more.

7. The organic electroluminescent device according to claim 1, characterized in that: The molecular weight of the compound represented by [Chemical Formula A] is 650 or more.

8. The organic electroluminescent device according to claim 1, characterized in that: The solvent includes at least one of chlorine solvents, ether solvents, aromatic solvents, aliphatic solvents, ketone solvents, ester solvents, alcohol solvents, amide solvents and benzoate solvents.

9. The organic electroluminescent device according to claim 1, characterized in that: The host represented by [Chemical Formula A] is dissolved in the solvent in an amount of 1 weight percent or more.

10. The organic electroluminescent device according to claim 1, characterized in that: The host represented by [Chemical Formula A] is represented by any one of the following [1] to [30]:

11. The organic electroluminescent device according to claim 1, characterized in that: The [Chemical Formula B-1] and [Chemical Formula B-2] contain at least one -N(R")2.

12. The organic electroluminescent device according to claim 1, characterized in that: The dopant represented by [Chemical Formula B-1] or [Chemical Formula B-2] is represented by any one of the following [D 1] to [D 154]:

13. The organic electroluminescent device according to claim 1, characterized in that: In addition to the light-emitting layer, the organic layer further includes at least one of a hole injection layer, a hole transport layer, a functional layer having both hole injection and hole transport functions, an electron transport layer, and an electron injection layer.

14. The organic electroluminescent device according to claim 1, characterized in that: The organic layer is formed by any one of spin coating, dip coating, blade coating, spray coating, roll coating, inkjet printing, and screen printing.

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