KR102005867B1 - Composition for organic optoelectronic device and organic optoelectronic device and display device - Google Patents

Abstract

At least one first host compound represented by Formula 1; And at least one second host compound represented by the general formula (2), and an organic optoelectronic device and a display device to which the organic optoelectronic device and the organic optoelectronic device are applied.
Details of the above Formulas 1 and 2 are as defined in the specification.

Description

Technical Field The present invention relates to a composition for an organic optoelectronic device, an organic optoelectronic device, and a display device. BACKGROUND OF THE INVENTION 1. Field of the Invention [0001]

A composition for organic optoelectronic devices, an organic optoelectronic device and a display device.

An organic optoelectronic diode is an element that can switch between electric energy and light energy.

Organic optoelectronic devices can be roughly classified into two types according to the operating principle. One is an optoelectronic device in which an exciton formed by light energy is separated into an electron and a hole, the electron and hole are transferred to different electrodes to generate electric energy, and the other is a voltage / Emitting device that generates light energy from energy.

Examples of organic optoelectronic devices include organic optoelectronic devices, organic light emitting devices, organic solar cells, and organic photo conductor drums.

In recent years, organic light emitting diodes (OLEDs) have attracted considerable attention due to the demand for flat panel display devices. The organic light emitting diode is a device for converting electrical energy into light by applying an electric current to the organic light emitting material, and usually has an organic layer inserted between an anode and a cathode. The organic layer may include a light emitting layer and an optional auxiliary layer. The auxiliary layer may include, for example, a hole injecting layer, a hole transporting layer, an electron blocking layer, an electron transporting layer, And a hole blocking layer.

The performance of the organic light emitting device is greatly influenced by the characteristics of the organic layer, and the organic layer is highly affected by the organic material contained in the organic layer.

In particular, in order for the organic light emitting device to be applied to a large-sized flat panel display device, it is necessary to develop an organic material capable of increasing the mobility of holes and electrons and increasing the electrochemical stability.

One embodiment provides a composition for an organic optoelectronic device capable of implementing a high-efficiency and long-lived organic optoelectronic device.

Another embodiment provides an organic optoelectronic device comprising the composition.

Another embodiment provides a display device comprising the organic opto-electronic device.

According to one embodiment, at least one first host compound represented by the following formula (1); And at least one second host compound represented by the following general formula (2).

[Chemical Formula 1]

In Formula 1,

Z ¹ to Z ⁵ are each independently N or CR ^a ,

At least one of Z ¹ to Z ⁵ is N,

R ^a and R ¹ to R ³ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, Or a combination thereof,

R ^a may be independently present or adjacent R ^{a may be} connected to form a substituted or unsubstituted aliphatic, aromatic or heteroaromatic monocyclic or polycyclic ring,

L is a single bond, a substituted or unsubstituted C6 to C30 arylene group, a substituted or unsubstituted C2 to C30 heteroarylene group, or a combination thereof;

(2)

In Formula 2,

R ⁴ to R ⁹ each independently represent hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, ego,

Y ¹ and Y ² are each independently a single bond, a substituted or unsubstituted C6 to C30 arylene group, a substituted or unsubstituted C2 to C30 heteroarylene group, or a combination thereof,

Ar ¹ and Ar ² are each independently a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,

m is an integer of 0 to 2,

"Substitution" in the above formulas (1) and (2) means that at least one hydrogen is substituted with deuterium, C1 to C4 alkyl group, C6 to C18 aryl group or C2 to C18 heteroaryl group.

According to another embodiment, there is provided an organic electroluminescent device including an anode and a cathode facing each other, and at least one organic layer positioned between the anode and the cathode, wherein the organic layer comprises an organic optoelectronic device including the above composition for an organic optoelectronic device do.

According to another embodiment, there is provided a display device including the organic optoelectronic device.

High-efficiency long-lived organic optoelectronic devices can be realized.

1 and 2 are cross-sectional views illustrating an organic light emitting device according to one embodiment.

Hereinafter, embodiments of the present invention will be described in detail. However, it should be understood that the present invention is not limited thereto, and the present invention is only defined by the scope of the following claims.

As used herein, unless otherwise defined, at least one hydrogen in the substituent or compound is replaced with a substituent selected from the group consisting of deuterium, a halogen group, a hydroxyl group, an amino group, a substituted or unsubstituted C1 to C30 amine group, a nitro group, A C1 to C30 alkyl group, a C1 to C10 alkylsilyl group, a C6 to C30 arylsilyl group, a C3 to C30 cycloalkyl group, a C3 to C30 heterocycloalkyl group, a C6 to C30 aryl group, a C2 to C30 aryl group, A C1 to C20 alkoxy group, a C1 to C10 trifluoroalkyl group, a cyano group, or a combination thereof.

"Substitution" in the context of the present invention means that at least one hydrogen in the substituent or compound is substituted with deuterium, a C1 to C10 alkyl group, a C6 to C30 aryl group, a C2 to C30 heterocyclic group, or a combination thereof.

More specifically, "substituted" means that at least one hydrogen is substituted with deuterium, a C1 to C4 alkyl group, a C6 to C18 aryl group, or a C2 to C18 heteroaryl group.

Two adjacent substituents may also be linked to form a fused ring. For example, quinoline, isoquinoline, quinazoline, benzofuranpyrimidine, benzothiophene pyrimidine, fluorene and the like can be formed.

Means one to three heteroatoms selected from the group consisting of N, O, S, P and Si in one functional group, and the remainder being carbon unless otherwise defined .

As used herein, the term "alkyl group" means an aliphatic hydrocarbon group, unless otherwise defined. The alkyl group may be a "saturated alkyl group" which does not contain any double or triple bonds.

The alkyl group may be an alkyl group of C1 to C30. More specifically, the alkyl group may be a C1 to C20 alkyl group or a C1 to C10 alkyl group. For example, C1 to C4 alkyl groups mean that from 1 to 4 carbon atoms are included in the alkyl chain and include methyl, ethyl, propyl, iso-propyl, n-butyl, iso-butyl, sec- Indicating that they are selected from the group.

Specific examples of the alkyl group include a methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, t-butyl group, pentyl group, hexyl group, cyclopropyl group, cyclobutyl group, cyclopentyl group, And the like.

As used herein, the term " aryl group "refers to a grouping of groups having one or more hydrocarbon aromatic moieties,

A structure in which all the elements of the hydrocarbon aromatic moiety have a p-orbital and these p-orbital forms a conjugation, such as a phenyl group and a naphthyl group,

A structure in which two or more hydrocarbon aromatic moieties are connected through a sigma bond, such as a biphenyl group, a terphenyl group, a quarter-phenyl group,

Two or more hydrocarbon aromatic moieties may also include non-aromatic fused rings fused directly or indirectly. For example, a fluorenyl group and the like.

The aryl groups include monocyclic, polycyclic or fused ring polycyclic (i. E., Rings that divide adjacent pairs of carbon atoms) functional groups.

As used herein, the term " heterocyclic group "is a superordinate concept including a heteroaryl group, and includes N, O, and S substituents in the ring compound such as an aryl group, a cycloalkyl group, a fused ring thereof, Means at least one heteroatom selected from the group consisting of S, P and Si. When the heterocyclic group is a fused ring, the heterocyclic group or the ring may include one or more heteroatoms.

As used herein, the term " heteroaryl group "means that at least one heteroatom selected from the group consisting of N, O, S, P and Si is contained in the aryl group instead of carbon (C). Two or more heteroaryl groups may be directly connected through a sigma bond, or when the C2 to C60 heteroaryl group includes two or more rings, two or more rings may be fused with each other. When the heteroaryl group is a fused ring, it may contain 1 to 3 heteroatoms in each ring.

The heteroaryl group may include, for example, a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group and the like.

More specifically, the substituted or unsubstituted C6 to C30 aryl group and / or the substituted or unsubstituted C2 to C30 heterocyclic group may be substituted or unsubstituted phenyl group, substituted or unsubstituted naphthyl group, substituted or unsubstituted anthra A substituted or unsubstituted phenanthryl group, a substituted or unsubstituted naphthacenyl group, a substituted or unsubstituted pyrenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted p-terphenyl group, a substituted or unsubstituted naphthacenyl group, A substituted or unsubstituted thienyl group, a substituted m-terphenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted perylenyl group, a substituted or unsubstituted fluorenyl group, A substituted or unsubstituted thiophenyl group, a substituted or unsubstituted pyrrolyl group, a substituted or unsubstituted pyrazolyl group, a substituted or unsubstituted imidazolyl group, a substituted or unsubstituted furanyl group, a substituted or unsubstituted thiophenyl group, A substituted or unsubstituted thiazolyl group, a substituted or unsubstituted thiadiazolyl group, a substituted or unsubstituted thiazolyl group, a substituted or unsubstituted thiadiazolyl group, a substituted or unsubstituted thiazolyl group, a substituted or unsubstituted thiazolyl group, Substituted or unsubstituted benzothiophenyl groups, substituted or unsubstituted pyrazinyl groups, substituted or unsubstituted pyrazinyl groups, substituted or unsubstituted pyrazinyl groups, substituted or unsubstituted pyrazinyl groups, substituted or unsubstituted pyrazinyl groups, substituted or unsubstituted pyrazinyl groups, Substituted or unsubstituted quinazolinyl groups, substituted or unsubstituted quinazolinyl groups, substituted or unsubstituted quinolinyl groups, substituted or unsubstituted quinolinyl groups, substituted or unsubstituted quinazolinyl groups, substituted or unsubstituted quinazolinyl groups, A substituted or unsubstituted naphthyridinyl group, a substituted or unsubstituted benzoxazine group, a substituted or unsubstituted benzothiazine group, a substituted or unsubstituted acridinyl group, a substituted or unsubstituted naphthyridinyl group, A substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiazyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiazyl group, Substituted or unsubstituted benzofuranpyrimidines, substituted or unsubstituted benzothiophenepyrimidines, or combinations thereof, but is not limited thereto.

In the present specification, a single bond means a bond directly connected to a carbon atom or a hetero atom other than carbon. Specifically, L means a single bond, meaning that the substituent connected to L is directly connected to the center core do. That is, in the present specification, a single bond does not mean methylene or the like via carbon.

In the present specification, the hole property refers to a property of forming holes by donating electrons when an electric field is applied, and has a conduction property along the HOMO level so that the injection of holes formed in the anode into the light emitting layer, Quot; refers to the property of facilitating the movement of the hole formed in the light emitting layer to the anode and the movement of the hole in the light emitting layer.

In addition, the electron characteristic refers to a characteristic that electrons can be received when an electric field is applied. The electron characteristic has a conduction characteristic along the LUMO level so that electrons formed in the cathode are injected into the light emitting layer, electrons formed in the light emitting layer migrate to the cathode, It is a characteristic that facilitates movement.

Hereinafter, a composition for an organic optoelectronic device according to an embodiment will be described.

The composition for an organic optoelectronic device according to an embodiment includes at least two types of host and a dopant, and the host has a first host compound having a relatively high electron characteristic and a second host compound having a relatively high hole characteristic, Host compounds.

The first host compound is a compound having a relatively strong electron transporting property and is represented by the following formula (1).

[Chemical Formula 1]

In Formula 1,

Z ¹ to Z ⁵ are each independently N or CR ^a ,

At least one of Z ¹ to Z ⁵ is N,

R ^a and R ¹ to R ³ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, Or a combination thereof,

R ^a may be independently present or adjacent R ^{a may be} connected to form a substituted or unsubstituted aliphatic, aromatic or heteroaromatic monocyclic or polycyclic ring,

L is a single bond, a substituted or unsubstituted C6 to C30 arylene group, a substituted or unsubstituted C2 to C30 heteroarylene group, or a combination thereof.

The first host compound has a substantially linear structure including benzo [4,5] imidazo [1,2, f] phenanthridine and an ET group composed of Z ¹ to Z ⁵ , thereby self- Stability and thin film uniformity can be enhanced.

The first host compound is Z ¹ to Z ⁵ ET group 1-A for example to the formula, depending on the type of consisting of the formula 1-B, Formula 1-C, Formula 1-D, Formula 1-E, Formula 1-F , Formula (1-G) or formula (1-H).

[Chemical Formula 1-A] [Chemical Formula 1-B]

[Chemical Formula 1-C] [Chemical Formula 1-D]

[Chemical Formula 1-E] [Chemical Formula 1-F]

[Chemical Formula 1-G] [Chemical Formula 1-H]

R ¹ to R ³ , and L in Formula 1-A, Formula 1-B, Formula 1-C, Formula 1-D, Formula 1-E, Formula 1-F, Formula 1- Lt; / RTI > is as described above,

R ^a1 to R ^a5 are as defined in the above-mentioned R ^a , and W is O or S.

은 하기 그룹 Ⅰ에 나열된 치환기에서 선택될 수 있다.In one example of the present invention, the first host compound may be selected from, for example, the above-mentioned Formula 1-A, Formula 1-D, Formula 1-E and Formula 1-G, 1-D, or 1-G. More specifically,

May be selected from the substituents listed in Group I below.

[Group I]

In the above group I, * is a connection point.

The above formula (1) may be represented by the following formula (1a) or (1b) depending on the point of attachment of benzo [4,5] imidazo [1,2, f] phenanthridine.

[Chemical Formula 1a] [Chemical Formula 1b]

In the above general formulas (1a) and (1b), Z ¹ to Z ⁵ , R ¹ to R ³ , and L are as described above.

In one embodiment of the present invention, L may be a single bond, a substituted or unsubstituted phenylene group, a substituted or unsubstituted biphenylene group, a substituted or unsubstituted terphenylene group, or a combination thereof, A substituted or unsubstituted phenylene group, or a substituted or unsubstituted biphenylene group.

benzo [4,5] imidazo [1,2, f] phenanthridine and the ET group consisting of Z ¹ to Z ⁵ , that is, L is short, the molecular shape becomes closer to the spherical shape, Stability can be obtained.

Specifically, L may be selected from a single bond, or a substituted or unsubstituted linking group listed in Group II below,

[Group II]

Most specifically a single bond, an m-phenylene group, or a p-phenylene group.

In one embodiment of the present invention, each of R ¹ to R ³ may independently be hydrogen, deuterium, a methyl group, an ethyl group, a propyl group, an isopropyl group, a substituted or unsubstituted phenyl group, or a substituted or unsubstituted biphenyl group .

Each R ^a is independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, or a substituted or unsubstituted fluorenyl group, or adjacent R ^{a is} connected to be substituted or substituted May form a monocyclic or polycyclic ring of a substituted aliphatic, aromatic or heteroaromatic ring.

When the adjacent R ^a's are connected to form a substituted or unsubstituted aliphatic, aromatic or heteroaromatic monocyclic or polycyclic ring, for example, the above-mentioned formula 1-E, formula 1-F, formula 1 -G or formula 1 -H . ≪ / RTI >

More specifically, wherein R ¹ to R ³ are all hydrogen, wherein R ^a is each independently a substituted or unsubstituted phenyl group, or a substituted or non-substituted or unsubstituted biphenyl group, R is ^a connection between a substituted or unsubstituted quinazolinyl A substituted or unsubstituted benzofuran-pyrimidinyl group, or a substituted or unsubstituted benzothiophenepyrimidinyl group.

The first host compound may be, for example, a compound listed in the following Group 1, but is not limited thereto.

[Group 1]

.

.

The second host compound is a compound having a relatively strong hole transporting property and is represented by the following formula (2).

(2)

In Formula 2,

R ⁴ to R ⁹ each independently represent hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, ego,

Y ¹ and Y ² are each independently a single bond, a substituted or unsubstituted C6 to C30 arylene group, a substituted or unsubstituted C2 to C30 heteroarylene group, or a combination thereof,

Ar ¹ and Ar ² are each independently a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,

m is an integer of 0 to 2;

The compound for the second organic optoelectronic device is a compound having a relatively strong hole property and is used in the light emitting layer together with the compound for the first organic optoelectronic device to increase the charge mobility and increase the stability, Can be improved. Further, the charge mobility can be controlled by controlling the ratio of the compound for the second organic optoelectronic device having the hole characteristic to the compound for the first organic optoelectronic device.

In one embodiment of the present invention, Ar ¹ and Ar ² in Formula 2 are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted naphthyl group A substituted or unsubstituted thiophene group, a substituted or unsubstituted thiophene group, a substituted or unsubstituted anthracenyl group, a substituted or unsubstituted triphenylenyl group, a substituted or unsubstituted pyridinyl group, a substituted or unsubstituted pyrimidinyl group, A substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted fluorenyl group, or a combination thereof,

Specifically, the formula (2) is one of the structures listed in the following Group III, and * -Y ¹ -Ar ¹ and * -Y ² -Ar ² may be any of the substituents listed in the following Group IV.

[Group III]

[Group IV]

In the groups III and IV, * is a connection point.

For example, Ar ¹ and Ar ² may each independently be a phenyl group, a biphenyl group, a dibenzofuranyl group, or a dibenzothiophen yl group.

The second host compound may be, for example, a compound listed in the following Group 2, but is not limited thereto.

[Group 2]

[B-1] [B-2] [B-3]

[B-4] [B-5] [B-6]

[B-7] [B-8] [B-9]

[B-10] [B-11] [B-12]

[B-13] [B-14] [B-15]

[B-16] [B-17] [B-18]

[B-19] [B-20] [B-21]

[B-22] [B-23] [B-24]

[B-25] [B-26] [B-27]

[B-28] [B-29] [B-30] [B-31]

[B-33] [B-34] [B-35]

[B-36] [B-37] [B-38]

[B-39] [B-40] [B-41]

[B-42] [B-43] [B-44]

[B-45] [B-46] [B-47]

[B-48] [B-49] [B-50]

[B-51] [B-52] [B-53]

[B-54] [B-55] [B-56]

[B-57] [B-58] [B-59]

[B-60] [B-61] [B-62]

[B-63] [B-64] [B-65]

[B-66] [B-67] [B-68]

[B-69] [B-70] [B-71]

[B-72] [B-73] [B-74]

[B-75] [B-76] [B-77]

[B-78] [B-79] [B-80]

[B-81] [B-82] [B-83]

[B-84] [B-85] [B-86]

[B-87] [B-88] [B-89]

[B-90] [B-91] [B-92]

[B-93] [B-94] [B-95]

[B-96] [B-97] [B-98] [B-99]

[B-101] [B-102] [B-103]

[B-104] [B-105] [B-106]

[B-107] [B-108] [B-109]

[B-110] [B-111] [B-112]

[B-113] [B-114] [B-115]

[B-116] [B-117] [B-118]

[B-119] [B-120] [B-121]

[B-122] [B-123] [B-124]

[B-125] [B-126] [B-127]

[B-128] [B-129] [B-130]

[B-131] [B-132] [B-133] [B-134]

[B-135] [B-136] [B-137] [B-138]

The first host compound and the second host compound described above can be prepared in various compositions in various combinations.

The composition according to one embodiment of the present invention comprises as a first host the compound represented by Formula 1-A, Formula 1-D, or Formula 1-G, and the compound represented by Formula c-8 or Formula c- 17 as a second host.

For example, a first host represented by any one of the above-mentioned Formulas 1-A, 1-D and 1-G and a second host represented by the formula c-8 in Group III, And a second host represented by the formula c-17 of the group III.

* -Y ¹ -Ar ¹ and * -Y ² -Ar ² in the above formula (2) can be selected, for example, from B-1, B-2, B-3 and B-16 of the group IV.

As described above, the first host compound is a compound having a relatively strong electron transporting property and the second host compound is a compound having a relatively high hole transporting property, and when they are used alone by being used together, or The luminous efficiency can be remarkably improved by increasing the mobility of electrons and holes compared with mixed hosts of other combinations.

The first host compound and the second host compound may be contained in a weight ratio of, for example, 1:10 to 10: 1. For example, in the range of 2: 8 to 8: 2, 3: 7 to 7: 3, 4: 6 to 6: 4, and 5: . ≪ / RTI > By being included in the above range, the bipolar characteristic can be implemented more effectively, and the efficiency and lifetime can be simultaneously improved.

The composition may further include at least one host compound in addition to the first host compound and the second host compound.

The composition may further comprise a dopant. The dopant may be a red, green or blue dopant, for example a phosphorescent dopant.

The dopant may be a metal complex that emits light by multiple excitation that is excited by a triplet state or higher, and is a substance that emits light by mixing with the first host compound and the second host compound. May be used. The dopant may be, for example, an inorganic, organic, or organic compound, and may include one or more species.

Examples of the phosphorescent dopant include organic metal compounds including Ir, Pt, Os, Ti, Zr, Hf, Eu, Tb, Tm, Fe, Co, Ni, Ru, Rh and Pd or combinations thereof. The phosphorescent dopant may be, for example, a compound represented by the following formula (Z), but is not limited thereto.

(Z)

L ₂ MX

In the above formula (Z), M is a metal, L and X are the same or different from each other and are ligands that complex with M.

M may be Ir, Pt, Os, Ti, Zr, Hf, Eu, Tb, Tm, Fe, Co, Ni, Ru, Rh, Pd or combinations thereof, Lt; / RTI >

The composition may be formed by a dry film forming method such as chemical vapor deposition or a solution process.

Hereinafter, an organic optoelectronic device according to another embodiment will be described.

An organic optoelectronic device according to another embodiment includes an anode and a cathode facing each other, and at least one organic layer positioned between the anode and the cathode, and the organic layer may include the composition for the organic optoelectronic device described above .

Here, an organic light emitting device, which is an example of an organic optoelectronic device, will be described with reference to the drawings.

1 and 2 are cross-sectional views illustrating an organic light emitting device according to an embodiment.

1, an organic optoelectronic device 100 according to an embodiment includes an anode 120 and a cathode 110 facing each other, and an organic layer 105 located between the anode 120 and the cathode 110 .

The anode 120 may be made of a conductor having a high work function to facilitate, for example, hole injection, and may be made of, for example, a metal, a metal oxide, and / or a conductive polymer. The anode 120 is made of a metal such as nickel, platinum, vanadium, chromium, copper, zinc, gold, or an alloy thereof; Metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO); A combination of ZnO and Al or a metal and an oxide such as SnO ₂ and Sb; Conductive polymers such as poly (3-methylthiophene), poly (3,4- (ethylene-1,2-dioxy) thiophene), polypyrrole and polyaniline, It is not.

The cathode 110 may be made of a conductor having a low work function, for example, to facilitate electron injection, and may be made of, for example, a metal, a metal oxide, and / or a conductive polymer. The cathode 110 is made of a metal such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin, lead, cesium, barium or the like or an alloy thereof; Layer structure materials such as LiF / Al, LiO ₂ / Al, LiF / Ca, LiF / Al and BaF ₂ / Ca.

The organic layer 105 may include the composition for the organic optoelectronic device described above.

For example, the above-described composition for an organic optoelectronic device may be included as a host in the light emitting layer 130 included in the organic layer 105.

Referring to FIG. 2, the organic light emitting diode 200 further includes a hole-assist layer 140 in addition to the light-emitting layer 130. The hole auxiliary layer 140 can further enhance hole injection and / or hole mobility between the anode 120 and the light emitting layer 130 and block electrons. The hole-assist layer 140 may be, for example, a hole transport layer, a hole injection layer, and / or an electron blocking layer, and may include at least one layer.

In one embodiment of the present invention, the organic layer 105 may further include an electron transport layer, an electron injection layer, a hole injection layer, and the like, as shown in FIG. 1 or 2.

The organic light emitting devices 100 and 200 may be formed by forming an anode or a cathode on a substrate and then forming an organic layer by a dry film forming method such as evaporation, sputtering, plasma plating, or ion plating, A negative electrode or a positive electrode.

The organic light emitting device described above can be applied to an organic light emitting display.

Hereinafter, specific embodiments of the present invention will be described. However, the embodiments described below are only intended to illustrate or explain the present invention, and thus the present invention should not be limited thereto.

(Preparation of composition for organic optoelectronic device)

Hereinafter, the starting materials and the reaction materials used in Examples and Synthesis Examples were purchased from Sigma-Aldrich or TCI unless otherwise stated, and they are easily synthesized with known materials.

(Synthesis of first host compound)

Synthetic example  1: Synthesis of intermediate A

[Reaction Scheme 1]

Step 1: Synthesis of intermediate A-1

2-chloro-bromobenzene (200 g, 1.04 mol) and 2-formylphenylboronic acid (186.8 g, 1.24 mmol) were completely dissolved in 4 L of tetrahydrofuran, and then potassium carbonate (360 g, 2.6 mol) Tetraquistriphenylphosphinopalladium (24.2 g, 20.90 mmol) and 2 L of water were added thereto, followed by stirring and refluxing for 8 hours. The temperature was lowered to room temperature, the water layer was removed, and the organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure and subjected to column chromatography to obtain Intermediate A-1 (186 g, 82%).

Step 2: Synthesis of intermediate A-2

Intermediate A-1 (180.0 g, 0.84 mol) and 2-azido-5-chloroaniline (140.0 g, 0.84 mol) were suspended in 2.4 L of ethanol and 120 mL of acetic acid in a 5 L round bottom flask. The mixture was stirred and refluxed for 24 hours. The mixture was cooled to room temperature, concentrated under reduced pressure, and recrystallized from hexane to obtain Intermediate A-2 (68 g, 24%).

Step 3: Synthesis of intermediate A-3

A 2 L flask was charged with intermediate A-2 (67.0 g, 197.5 mmol), sodium tertiary-butoxide (38 g, 395.0 mmol) and tris (dibenzylideneacetone) dipalladium 11.4 g (19.8 mmol) 16 g (50% in toluene) of phosphine was mixed with 700 mL of xylene, heated under a nitrogen stream for 15 hours, refluxed and cooled to room temperature. Distilled water was added to the reaction solution, and the reaction was terminated. The organic layer was extracted, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure and column chromatography was used to obtain Intermediate A-3 (25.1 g, 42%).

Step 4: Synthesis of intermediate A

To a 1 L flask was added Intermediate A-3 (25.0 g, 82.6 mmol), 4,4,4 ', 4', 5,5,5 ', 5'-octamethyl-2,2'- (25.2 g, 99.1 mmol), potassium acetate (KOAc, 24.3 g, 247.7 mmol) and 1,1'-bis (diphenylphosphino) ferrocene-palladium (II) dichloride 4.6 mmol) and tricyclohexylphosphine (6.9 g, 12.4 mmol) were added to 400 mL of N, N-dimethylformamide, and the mixture was stirred at 130 占 폚 for 24 hours. After completion of the reaction, the reaction solution was extracted with water and EA. The obtained organic layer was washed with water using magnesium sulfate, concentrated and purified by column chromatography to obtain Intermediate A (27.7 g, yield = 85%).

calcd. C25H23BN2O2: C, 76.16; H, 5.88; B, 2.74; N, 7.11; 0, 8.12; found: C, 76.15; H, 5.88; B, 2.74; N, 7.10; O, 8.12

Synthetic example  2: Intermediate Of B  synthesis

[Reaction Scheme 2]

Step 1: Synthesis of intermediate B-1

Intermediate A-1 (180.0 g, 0.84 mol) and 2-azido-4-chlorobenzeneamine (140.0 g, 0.84 mol) were suspended in 2.4 L of ethanol and 120 mL of acetic acid in a 5 L round bottom flask. The mixture was stirred and refluxed for 24 hours. The mixture was cooled to room temperature, concentrated under reduced pressure, and recrystallized with hexane to obtain Intermediate B-1 (84 g, 30%).

Step 2: Synthesis of intermediate B-2

A 2 L flask was charged with intermediate B-1 (83.0 g, 244.8 mmol), sodium tertiary butoxide (47 g, 489.5 mmol) and tris (dibenzylideneacetone) dipalladium 14.1 g (24.5 mmol) 19.8 g (50% in toluene) of phosphine was mixed with 1 L of xylene, heated under a nitrogen stream for 15 hours, refluxed and cooled to room temperature. Distilled water was added to the reaction solution, and the reaction was terminated. The organic layer was extracted, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure and column chromatography was used to obtain Intermediate B-2 (30.0 g, 40%).

Step 3: Synthesis of intermediate B

To a 1 L flask was added intermediate B-2 (30.0 g, 99.1 mmol), 4,4,4 ', 4', 5,5,5 ', 5'-octamethyl-2,2'- (30.2 g, 118.9 mmol), potassium acetate (KOAc, 29.2 g, 297.3 mmol) and 1,1'-bis (diphenylphosphino) ferrocene-palladium (II) dichloride (4.9 g, 5.9 mmol) and tricyclohexylphosphine (8.3 g, 14.9 mmol) were placed in N, N-dimethylformamide (500 mL), and the mixture was stirred at 130 DEG C for 24 hours. After completion of the reaction, the reaction solution was extracted with water and EA. The obtained organic layer was extracted with water using magnesium sulfate, concentrated and purified by column chromatography to obtain Intermediate B (31.3 g, yield = 80%).

calcd. C25H23BN2O2: C, 76.16; H, 5.88; B, 2.74; N, 7.11; 0, 8.12; Found: C, 76.16; H, 5.88; B, 2.74; N, 7.10; O, 8.11

Synthetic example  3: Synthesis of Compound 1-1

[Reaction Scheme 3]

Synthesis of Compound 1-1

Intermediate 1 (2.5 g, 9.3 mmol), Intermediate A (4.4 g, 11.2 mmol), potassium carbonate (3.2 g, 23.4 mmol) and tetrakis (triphenylphosphine) palladium (0) mmol) was added to 30 mL of 1,4-dioxane and 15 mL of water, and the mixture was heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated, and 300 mL of methanol was added thereto. The crystallized solid was filtered, dissolved in 1,2-dichlorobenzene, filtered through silica gel / celite, an organic solvent was removed in an appropriate amount, and the residue was recrystallized from monochlorobenzene, 1 (3.7 g, 79% yield).

calcd. For C34H21N5: C, 81.74; H, 4.24; N, 14.02; found: C, 81.74; H, 4.24; N, 14.02

Synthetic example  4: Synthesis of Compound 1-2

[Reaction Scheme 4]

Synthesis of intermediate 3

To a 1 L round bottom flask was added 30.0 g (132.7 mmol) of Intermediate 2, 25.0 g (126.0 mmol) of 3-biphenylboronic acid, 45.8 g (230.0 mmol) of potassium carbonate, 4.0 g of tetrakis (triphenylphosphine) palladium (4.6 mmol) were added to 1,440-dioxane (440 mL) and water (220 mL), and the mixture was heated under reflux in a nitrogen stream for 6 hours. The organic layer was separated and added to 2 L of methanol. The resulting solid was filtered, dissolved in monochlorobenzene, filtered through silica gel / celite, and then an organic solvent was removed in an appropriate amount and then recrystallized as monochlorobenzene to obtain Intermediate 3 (24.9 g, 55% Yield).

Synthesis of Compound 1-2

(2.5 g, 7.3 mmol), Intermediate A (3.4 g, 8.7 mmol), potassium carbonate (2.5 g, 18.2 mmol) and tetrakis (triphenylphosphine) palladium (0) mmol) were added to 24 mL of 1,4-dioxane and 12 mL of water and then heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated and added to 150 mL of methanol. The crystallized solid was filtered and dissolved in 1,2-dichlorobenzene, filtered through silica gel / celite, an organic solvent was removed in an appropriate amount and then recrystallized from monochlorobenzene to obtain Compound 1- 2 (3.2 g, 76% yield).

calcd. For C40H25N5: C, 83.46; H, 4.38; N, 12.17; Found: C, 83.46; H, 4.38; N, 12.17

Synthetic example  5: Synthesis of Compound 1-3

[Reaction Scheme 5]

Synthesis of Intermediate 4

To a 1 L round bottom flask was added 30.0 g (132.7 mmol) of Intermediate 2, 25.0 g (126.0 mmol) of 4-biphenylboronic acid, 45.8 g (230.0 mmol) of potassium carbonate, 4.0 g of tetrakis (triphenylphosphine) palladium (4.6 mmol) were added to 1,440-dioxane (440 mL) and water (220 mL), and the mixture was heated under reflux in a nitrogen stream for 6 hours. The organic layer was separated and added to 2 L of methanol. The resulting solid was filtered, dissolved in monochlorobenzene, filtered through silica gel / celite, and the organic solvent was removed in an appropriate amount and then recrystallized from monochlorobenzene to obtain Intermediate 4 (27.1 g, 60% Yield).

Synthesis of Compound 1-3

(2.5 g, 7.3 mmol), intermediate A (3.4 g, 8.7 mmol), potassium carbonate (2.5 g, 18.2 mmol) and tetrakis (triphenylphosphine) palladium (0) mmol) were added to 24 mL of 1,4-dioxane and 12 mL of water and then heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated and added to 150 mL of methanol, and the crystallized solid was filtered, dissolved in 1,2-dichlorobenzene, filtered through silica gel / cellite, an organic solvent was removed in an appropriate amount, and recrystallized with 1,2- To give compound 1-3 (3.1 g, 78% yield).

calcd. For C40H25N5: C, 83.46; H, 4.38; N, 12.17; Found: C, 83.45; H, 4.38; N, 12.18

Synthetic example  6: Synthesis of Compound 1-7

[Reaction Scheme 6]

Synthesis of Compound 1-7

Intermediate 5 (3.0 g, 7.7 mmol), Intermediate A (3.7 g, 9.3 mmol), potassium carbonate (2.7 g, 19.3 mmol) and tetrakis (triphenylphosphine) palladium (0) mmol) was added to 30 mL of 1,4-dioxane and 15 mL of water, and the mixture was heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated and added to 150 mL of methanol, and the crystallized solid was filtered, dissolved in monochlorobenzene, filtered through silica gel / celite, an organic solvent was removed in an appropriate amount and then recrystallized from monochlorobenzene to obtain 3.6 g , 81% yield).

calcd. For C40H25N5: C, 83.46; H, 4.38; N, 12.17; Found: C, 83.46; H, 4.38; N, 12.17

Synthetic example  7: Synthesis of Compound 1-10

[Reaction Scheme 7]

Synthesis of Compound 1-10

Intermediate 6 (3.0 g, 7.7 mmol), Intermediate A (3.7 g, 9.3 mmol), potassium carbonate (2.7 g, 19.3 mmol) and tetrakis (triphenylphosphine) palladium (0) (0.27 g, 0.2 mmol) was added to 30 mL of 1,4-dioxane and 15 mL of water, and the mixture was heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated and added to 150 mL of methanol, and the crystallized solid was filtered, then dissolved in monochlorobenzene, filtered with silica gel / celite, an organic solvent was removed in an appropriate amount, and recrystallized from monochlorobenzene to obtain Compound 1-10 , 79% yield).

calcd. For C40H25N5: C, 83.46; H, 4.38; N, 12.17; Found: C, 83.45; H, 4.38; N, 12.17

Synthetic example  8: Compound 1- 17  synthesis

[Reaction Scheme 8]

Synthesis of Compound 1-17

Intermediate 1 (2.5 g, 9.3 mmol), Intermediate B (4.4 g, 11.2 mmol) and potassium carbonate (3.2 g, 23.4 mmol) were added to a 100 mL flask. Tetrakis (triphenylphosphine) palladium mmol) was added to 30 mL of 1,4-dioxane and 15 mL of water, and the mixture was heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated, and 300 mL of methanol was added thereto. The crystallized solid was filtered, dissolved in 1,2-dichlorobenzene, filtered through silica gel / celite, an organic solvent was removed in an appropriate amount, and the residue was recrystallized from monochlorobenzene, 17 (3.5 g, 74.7% yield).

calcd. For C34H21N5: C, 81.74; H, 4.24; N, 14.02; Found: C, 81.73; H, 4.24; N, 14.02

Synthetic example  9: Synthesis of Compound 1-18

[Reaction Scheme 9]

Synthesis of Compound 1-18

(2.5 g, 7.3 mmol), intermediate B (3.4 g, 8.7 mmol), potassium carbonate (2.5 g, 18.2 mmol) and tetrakis (triphenylphosphine) palladium (0) mmol) were added to 24 mL of 1,4-dioxane and 12 mL of water and then heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated and added to 150 mL of methanol. The crystallized solid was filtered and dissolved in 1,2-dichlorobenzene, filtered through silica gel / celite, an organic solvent was removed in an appropriate amount and then recrystallized from monochlorobenzene to obtain Compound 1- 18 (3.24 g, 77% yield).

calcd. For C40H25N5: C, 83.46; H, 4.38; N, 12.17; Found: C, 83.45; H, 4.38; N, 12.17

Synthetic example  10: Synthesis of Compound 1-19

[Reaction Scheme 10]

Synthesis of Compound 1-19

(2.5 g, 7.3 mmol), Intermediate B (3.4 g, 8.7 mmol), potassium carbonate (2.5 g, 18.2 mmol) and tetrakis (triphenylphosphine) palladium (0) mmol) were added to 24 mL of 1,4-dioxane and 12 mL of water and then heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated and added to 150 mL of methanol, and the crystallized solid was filtered, dissolved in 1,2-dichlorobenzene, filtered through silica gel / cellite, an organic solvent was removed in an appropriate amount, and recrystallized with 1,2- To obtain Compound 1-19 (2.9 g, 75% yield).

calcd. For C40H25N5: C, 83.46; H, 4.38; N, 12.17; Found: C, 83.46; H, 4.38; N, 12.18

Synthetic example  11: Synthesis of Compound 1-23

[Reaction Scheme 11]

Synthesis of Compound 1-23

To a 100 mL flask was added intermediate 5 (3.0 g, 7.7 mmol), intermediate B (3.7 g, 9.3 mmol), potassium carbonate (2.7 g, 19.3 mmol) and tetrakis (triphenylphosphine) palladium (0) mmol) was added to 30 mL of 1,4-dioxane and 15 mL of water, and the mixture was heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated, and 150 mL of methanol was added thereto. The crystallized solid was filtered, dissolved in monochlorobenzene, filtered through silica gel / celite, an organic solvent was removed in an appropriate amount, and recrystallized from monochlorobenzene to obtain Compound 1-23 , 77% yield).

calcd. For C40H25N5: C, 83.46; H, 4.38; N, 12.17; Found: C, 83.45; H, 4.38; N, 12.17

Synthetic example  12: Synthesis of Compound 1-26

[Reaction Scheme 12]

Synthesis of Compound 1-26

To a 100 mL flask was added intermediate 6 (3.0 g, 7.7 mmol), intermediate B (3.7 g, 9.3 mmol), potassium carbonate (2.7 g, 19.3 mmol) and tetrakis (triphenylphosphine) palladium (0) mmol) was added to 30 mL of 1,4-dioxane and 15 mL of water, and the mixture was heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated and 150 mL of methanol was added thereto. The crystallized solid component was filtered, and the filtrate was dissolved in monochlorobenzene. The filtrate was filtered through silica gel / celite, and an organic solvent was removed in an appropriate amount and then recrystallized from monochlorobenzene to obtain Compound 1-26 , 77% yield).

calcd. For C40H25N5: C, 83.46; H, 4.38; N, 12.17; Found: C, 83.46; H, 4.38; N, 12.17

Synthetic example  13: Synthesis of Compound 1-34

[Reaction Scheme 13]

Synthesis of Compound 1-34

(3.0 g, 8.75 mmol), Intermediate A (3.4 g, 8.75 mmol), potassium carbonate (3.0 g, 21.9 mmol) and tetrakis (triphenylphosphine) palladium (0) mmol) was added to 30 mL of 1,4-dioxane and 15 mL of water, and the mixture was heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated and added to 150 mL of methanol. The crystallized solid was filtered and dissolved in 1,2-dichlorobenzene, filtered through silica gel / celite, an organic solvent was removed in an appropriate amount and then recrystallized from monochlorobenzene to obtain Compound 1- 34 (3.8 g, 76% yield).

calcd. For C41H26N4: C, 85.69; H, 4.56; N, 9.75; Found: C, 85.69; H, 4.56; N, 9.76

Synthetic example  14: Synthesis of Compound 1-39

[Reaction Scheme 14]

Synthesis of Compound 1-39

Intermediate 7 (3.0 g, 8.75 mmol), intermediate B (3.4 g, 8.75 mmol) and potassium carbonate (3.0 g, 21.9 mmol) were added to a 100 mL flask. Tetrakis (triphenylphosphine) palladium (0) mmol) was added to 30 mL of 1,4-dioxane and 15 mL of water, and the mixture was heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated and added to 150 mL of methanol. The crystallized solid was filtered and dissolved in 1,2-dichlorobenzene, filtered through silica gel / celite, an organic solvent was removed in an appropriate amount and then recrystallized from monochlorobenzene to obtain Compound 1- 39 (3.4 g, 68% yield).

calcd. For C41H26N4: C, 85.69; H, 4.56; N, 9.75; Found: C, 85.68; H, 4.56; N, 9.75

Synthetic example  15: Synthesis of Compound 1-46

[Reaction Scheme 15]

Synthesis of Compound 1-46

Intermediate 8 (3.0 g, 8.3 mmol), Intermediate A (3.27 g, 8.3 mmol), potassium carbonate (2.87 g, 20.8 mmol) and tetrakis (triphenylphosphine) palladium (0) (0.29 g, 0.25 mmol) was added to 30 mL of 1,4-dioxane and 15 mL of water, and the mixture was heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated and added to 150 mL of methanol. The crystallized solid was filtered and dissolved in 1,2-dichlorobenzene, filtered through silica gel / celite, an organic solvent was removed in an appropriate amount and then recrystallized from monochlorobenzene to obtain Compound 1- 46 (3.6 g, 79% yield).

calcd. For C39H24N4: C, 85.38; H, 4.41; N, 10.21; Found: C, 85.37; H, 4.40; N, 10.21

Synthetic example  16: Synthesis of Compound 1-54

[Reaction Scheme 16]

Synthesis of Compound 1-54

Intermediate 9 (3.0 g, 8.1 mmol), Intermediate A (3.17 g, 8.1 mmol), potassium carbonate (2.78 g, 20.1 mmol) and tetrakis (triphenylphosphine) palladium (0) (0.28 g, 0.24 mmol) was added to 30 mL of 1,4-dioxane and 15 mL of water, and the mixture was heated to 70 DEG C for 12 hours under a nitrogen stream. The organic layer was separated and added to 150 mL of methanol. The crystallized solid was filtered and dissolved in 1,2-dichlorobenzene, filtered through silica gel / celite, an organic solvent was removed in an appropriate amount and then recrystallized from monochlorobenzene to obtain Compound 1- 54 (3.5 g, 72% yield).

calcd. For C41H24N4S: C, 81.43; H, 4.00; N, 9.26; S, 5.30; found: C, 81.43; H, 3.99; N, 9.26; S, 5.30

(Synthesis of second host compound)

Synthetic example  17: Synthesis of compound B-129

[Reaction Scheme 17]

To a 500 mL round bottom flask equipped with a stirrer under nitrogen atmosphere, 20.00 g (42.16 mmol) of 3-bromo-6-phenyl-N-methabiphenylcarbazole and 17.12 g 1.46 g (1.26 mmol) of tetrakistriphenylphosphine palladium (0) was added to 175 ml of tetrahydrofuran: toluene (1: 1) and 75 ml of 2M potassium carbonate aqueous solution, The mixture was heated to reflux for 12 hours. After completion of the reaction, the reaction product was poured into methanol to filter the solid, and the obtained solid was sufficiently washed with water and methanol, and dried. The resulting solution was heated to 700 mL of chlorobenzene and then the solution was filtered through silica gel to remove the solvent completely. The solvent was then completely dissolved in 400 mL of chlorobenzene by heating and then recrystallized to obtain 18.52 g (yield 69%) of the compound B-129 .

calcd. C ₄₂ H ₃₂ N ₂ : C, 90.54; H, 5.07; N, 4.40; Found: C, 90.54; H, 5.07; N, 4.40

Synthetic example  18: Synthesis of compound B-137

[Reaction Scheme 18]

In a 250 mL round flask, 6.3 g (15.4 mmol) of N-phenyl-3,3-biscarbazole, 5.0 g (15.4 mmol) of 4- (4-bromophenyl) dibenzo [b, 1.2 g (50% in toluene) of tri (t-butylphosphine) and 0.9 g (1.5 mmol) of tris (dibenzylideneacetone) dipentaerythritol were mixed with 100 mL of xylene, Under reflux for 15 hours. The resulting solid was dissolved in dichlorobenzene, filtered through silica gel / celite, and the organic solvent was removed in an appropriate amount. The residue was recrystallized from methanol to obtain 7.3 g of intermediate B-137 , 73% yield).

calcd. For C48H30N2O: C, 88.59; H, 4.65; N, 4.30; O, 2.46; Found: C, 88.56; H, 4.62; N, 4.20; O, 2.43

compare Synthetic example : Synthesis of Compound E-1

[Reaction Scheme 19]

Synthesis of intermediate 2

30.0 g (104.5 mmol) of the starting material 1, 38.4 g (135.8 mmol) of 1-bromo-4-iodobenzene, 36.1 g (261.2 mmol) of potassium carbonate, tetrakis 0) was dissolved in 280 mL of 1,4-dioxane and 140 mL of water, and the mixture was heated to 80 DEG C for 16 hours under a nitrogen stream. The resultant mixture was added to 1200 mL of methanol, and the resulting solid was filtered. The resulting solid was dissolved in monochlorobenzene, filtered through silica gel / celite, and the organic solvent was removed in an appropriate amount. The residue was recrystallized from methanol to obtain 29.1 g % Yield).

calcd. For C24H16BrN: C, 72.37; H, 4.05; Br, 20.06; N, 3.52; found: C, 72.38; H, 4.06; Br, 20.05; N, 3.51

Intermediate E- Of PH  synthesis

To a 250 mL round flask was added 10.02 g (39.11 mmol) of Intermediate E, 7.32 g (46.9 mmol) of bromobenzene, 3.29 g (58.66 mmol) of potassium hydroxide, 1.49 g (7.82 mmol) of copper iodide And 10.41 g (7.82 mmol) of 10-phenanthroline were placed in 100 mL of DMSO, and the mixture was heated under reflux in a nitrogen stream for 15 hours. The resulting mixture was added to 500 mL of water, and the crystallized solid was filtered. The resulting solid was dissolved in dichlorobenzene, filtered through silica gel / celite, and the organic solvent was removed in an appropriate amount, followed by recrystallization from methanol to obtain an intermediate (8.4 g, 65% Yield of E-PH.

calcd. For C24H16N2: C, 86.72; H, 4.85; N, 8.43; found: C, 86.71; H, 4.86; N, 8.43

Synthesis of Compound E-1

To a 250 mL round flask was added 8.39 g (25.26 mmol) of Intermediate E-PH, 10.03 g (25.26 mmol) of Intermediate 2, 4.86 g (50.52 mmol) of sodium t-butoxide and 1.45 g 2.53 mmol) and tri-t-butylphosphine (2.0 mL, 50% in toluene) were placed in 120 mL of xylene and heated under reflux for 15 hours under a nitrogen stream. The resulting solid was dissolved in dichlorobenzene, filtered through silica gel / celite, and the organic solvent was removed in an appropriate amount, followed by recrystallization from methanol to obtain 8.0 g of compound E-1 , 49% yield).

calcd. For C48H31N3: C, 88.72; H, 4.81; N, 6.47; found: C, 88.72; H, 4.81; N, 6.47

Fabrication of organic light emitting device

Example 1

Glass substrate coated with ITO (Indium tin oxide) thin film with thickness of 1500Å was washed with distilled water ultrasonic wave. After the distilled water was washed, the substrate was ultrasonically washed with a solvent such as isopropyl alcohol, acetone, or methanol, dried and transferred to a plasma cleaner, then the substrate was cleaned using oxygen plasma for 10 minutes, and the substrate was transferred to a vacuum deposition machine. N4, N4'-diphenyl-N4, N4'-bis (9-phenyl-9H-carbazol-3-yl) biphenyl-4,4'- Diamine (Compound A) was vacuum-deposited to form a hole injection hole having a thickness of 700 Å. The hole injection layer was formed by vacuum deposition of N4, N4'-diphenyl-N4 and N4'-bis (9- Layer was formed, and 1,4,5,8,9,11-hexaazatriphenylene-hexacarbonitrile (1,4,5,8,9,11-hexaazatriphenylene-hexacarbonitrile, HAT-CN ) (Compound B) was deposited to a thickness of 50 ANGSTROM and then N- (biphenyl-4-yl) -9,9-dimethyl-N- (4- Phenyl) -9H-fluorene-2-amine (N- (biphenyl-4-yl) -9,9- -fluorene-2-amine (Compound C) was deposited to a thickness of 1020 ANGSTROM to form a hole transport layer. The compound 1-1 and the compound B-136 synthesized as described above were used as a host at the same time, and 10 wt% of dopant trotris (4-methyl-2,5-diphenylpyridine) iridium (III) To form a 400 Å thick light emitting layer by vacuum deposition. Compound 1-1 and compound B-136 were used in a ratio of 3: 7.

Subsequently, 8- (4- (4- (naphthalen-2-yl) -6- (naphthalen-3-yl) -1,3,5-triazin- (Compound E) and Liq at the same time in the ratio of 1: 1 to 1: 1. 1 ratio to form an electron transport layer having a thickness of 300 ANGSTROM and an anode was formed by sequentially vacuum-depositing Liq 15 ANGSTROM and Al 1200 ANGSTROM on the electron transport layer to prepare an organic light emitting device.

The organic light emitting device has a structure having five organic thin film layers. Specifically,

EML [1-1: B-136: D = 3: 7: 10%] (400 Å) / E: Liq (300 Å) / Liq (15 Å) / ITO / A (700 Å) / B (50 Å) / C ) / Al (1200 ANGSTROM).

(X = weight ratio)

Examples 2 to 22

The organic luminescent devices of Examples 2 to 22 were fabricated in the same manner as in Example 1 using the respective hosts as shown in the following Table 1 instead of the compounds 1-1 and B-136 in the luminescent layer formation .

Comparative Example 1

Except that 4,4'-di (9H-carbazol-9-yl) biphenyl (4,4'-di (9H-carbazol-9-yl) biphenyl, CBP) An organic light emitting device was fabricated in the same manner as in Example 1.

Reference Example 1

An organic light emitting device was fabricated in the same manner as in Example 1 except that Compound E-1 was used instead of Compound 1-1 in forming the light emitting layer.

Reference Example 2

An organic light emitting device was fabricated in the same manner as in Example 1 except that Compound C-1 was used instead of Compound 1-1 in the formation of the light emitting layer.

evaluation

Emitting efficiency and lifetime characteristics of the organic light-emitting devices according to Examples 1 to 22, Comparative Example 1, and Reference Examples 1 and 2 were evaluated.

The specific measurement method is as follows, and the results are shown in Table 1.

(1) Measurement of change in current density with voltage change

For the organic light emitting device manufactured, the current flowing through the unit device was measured using a current-voltmeter (Keithley 2400) while raising the voltage from 0 V to 10 V, and the measured current value was divided by the area to obtain the result.

(2) Measurement of luminance change according to voltage change

For the organic light-emitting device manufactured, luminance was measured using a luminance meter (Minolta Cs-1000A) while increasing the voltage from 0 V to 10 V, and the result was obtained.

(3) Measurement of luminous efficiency

The current efficiency (cd / A) at the same current density (10 mA / cm 2) was calculated using the luminance, current density and voltage measured from the above (1) and (2).

(4) Roll-off measurement

The decrease in efficiency was calculated as% (Max value - value at 6000 cd / m ² / Max value) among the characteristic values of the above (3)

(5) Life measurement

The time at which the luminance (cd / m ² ) was maintained at 6000 cd / m ² and the current efficiency (cd / A) decreased to 97% was measured and the results were obtained.

The first host Second host First host:
Second host
(wt / wt) Driving
Voltage
(V) radiation
efficiency
(cd / A) Roll-off
(%) Lifetime T97
(h) Example 1 1-1 B-136 3: 7 3.98 46.3 13.5 158 Example 2 1-2 B-136 3: 7 3.77 47.8 14.8 175 Example 3 1-3 B-136 3: 7 3.71 46.8 15.0 171 Example 4 1-7 B-136 3: 7 4.07 47.9 10.1 177 Example 5 1-10 B-136 3: 7 4.01 46.4 11.4 167 Example 6 1-17 B-136 3: 7 3.89 43.1 14.5 141 Example 7 1-18 B-136 3: 7 3.73 44.2 15.4 164 Example 8 1-19 B-136 3: 7 3.69 44.5 15.6 159 Example 9 1-23 B-136 3: 7 4.00 44.7 11.3 167 Example 10 1-26 B-136 3: 7 3.96 44.0 11.9 156 Example 11 1-34 B-136 3: 7 4.21 47.0 8.7 128 Example 12 1-39 B-136 3: 7 4.13 45.0 9.3 131 Example 13 1-54 B-136 3: 7 3.96 46.8 9.7 173 Example 14 1-2 B-98 3: 7 3.85 46.4 12.0 170 Example 15 1-3 B-98 3: 7 3.64 48.2 13.7 172 Example 16 1-7 B-98 3: 7 3.58 47.3 13.9 174 Example 17 1-2 B-129 3: 7 3.89 46.6 13.0 174 Example 18 1-3 B-129 3: 7 3.82 47.8 14.6 173 Example 19 1-7 B-129 3: 7 3.76 47.2 14.4 175 Example 20 1-2 B-137 3: 7 3.85 47.3 12.9 170 Example 21 1-3 B-137 3: 7 3.75 48.1 14.1 177 Example 22 1-7 B-137 3: 7 3.72 47.5 13.8 178 Comparative Example 1 CBP - - 5.21 35.1 5.3 105 Reference Example 1 E-1 B-136 3: 7 4.31 42.2 - 125 Reference Example 2 C-1 B-136 3: 7 4.61 40.5 - 113

Referring to Table 1, the organic light emitting devices according to Examples 1 to 22 exhibited remarkably improved driving voltage, luminous efficiency, and lifetime characteristics at the same time as those of the organic light emitting device according to Comparative Example 1 and Reference Examples 1 and 2 Can be confirmed.

It will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the spirit and scope of the present invention as defined by the following claims. As will be understood by those skilled in the art. It is therefore to be understood that the above-described embodiments are illustrative in all aspects and not restrictive.

100, 200: Organic light emitting device
105: organic layer
110: cathode
120: anode
130: light emitting layer
140: hole assist layer

Claims (14)

At least one first host compound represented by Formula 1 below; And
At least one second host compound represented by the following general formula (2)
Wherein the organic photovoltaic device comprises:
[Chemical Formula 1]

In Formula 1,
R ¹ to R ³ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof,
L is a single bond or a substituted or unsubstituted C6 to C30 arylene group;

Is represented by any one of substituent 1-A, substituent 1-B, substituent 1-C, substituent 1-D, substituent 1-G and substituent 1-H,
[Substituent group 1-A] [Substituent group 1-B] [Substituent group 1-C] [Substituent group 1-D]

In the substituents 1-A, 1-B, 1-C, 1-D, 1-G and 1-H,
R ^a1 to R ^a4 are each independently hydrogen, deuterium or a substituted or unsubstituted C6 to C30 aryl group,
W is O or S;
(2)

In Formula 2,
R ⁴ to R ⁹ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group or a combination thereof,
Y ¹ and Y ² are each independently a single bond or a substituted or unsubstituted C6 to C30 arylene group,
Ar ¹ and Ar ² are each independently a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof,
"Substitution" in the above formulas (1) and (2) means that at least one hydrogen is substituted with deuterium, C1 to C4 alkyl group, C6 to C18 aryl group or C2 to C18 heteroaryl group. delete The method according to claim 1,
Wherein the first host compound is represented by the following formula (1a) or (1b):
[Chemical Formula 1a] [Chemical Formula 1b]

In the above general formulas (1a) and (1b)
R ¹ to R ³ are each independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof,
L is a single bond or a substituted or unsubstituted C6 to C30 arylene group,

Is represented by any one of substituent 1-A, substituent 1-B, substituent 1-C, substituent 1-D, substituent 1-G and substituent 1-H,
[Substituent group 1-A] [Substituent group 1-B] [Substituent group 1-C] [Substituent group 1-D]

In the substituents 1-A, 1-B, 1-C, 1-D, 1-G and 1-H,
R ^a1 to R ^a4 are each independently hydrogen, deuterium or a substituted or unsubstituted C6 to C30 aryl group,
W is O or S. The method according to claim 1,
remind

Is one selected from the substituents listed in the following Group < RTI ID = 0.0 > I: < / RTI &
[Group I]

In the above group I, * is a connection point. The method according to claim 1,
Wherein L is a single bond, a substituted or unsubstituted phenylene group, a substituted or unsubstituted biphenylene group, a substituted or unsubstituted terphenylene group, or a combination thereof. The method according to claim 1,
Each of R ¹ to R ³ is independently hydrogen, deuterium, methyl, ethyl, propyl, isopropyl, substituted or unsubstituted phenyl or substituted or unsubstituted biphenyl,
Wherein R ^a1 to R ^a4 each independently represent hydrogen, a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, or a substituted or unsubstituted fluorenyl group . The method according to claim 1,
Wherein the organic compound is one selected from the compounds listed in the following Group 1:
[Group 1]

. The method according to claim 1,
Ar ¹ and Ar ² in Formula 2 are each independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted A substituted or unsubstituted dibenzothiophenylene group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted dibenzothiophenylene group, a substituted or unsubstituted dibenzofuranyl group, An organic group, an organic group, an organic group, 9. The method of claim 8,
Wherein * -Y ¹ -Ar ¹ and * -Y ² -Ar ² are one of the substituents listed in the following Group IV:
[Group IV]

In the above group IV, * is a connection point. 10. The method of claim 9,
Wherein * -Y ¹ -Ar ¹ and * -Y ² -Ar ² are B-1, B-2, B-3, or B-16 of Group IV. Positive and negative facing each other, and
And at least one organic layer positioned between the anode and the cathode,
Wherein the organic layer comprises the composition for organic optoelectronic devices according to any one of claims 1 to 10. 12. The method of claim 11,
Wherein the organic layer includes a light emitting layer,
Wherein the light emitting layer comprises the composition for the organic optoelectronic device. 13. The method of claim 12,
Wherein the composition for the organic optoelectronic device is included as a host of the light emitting layer. 12. A display device comprising the organic electroluminescent device according to claim 11.

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