KR101174083B1 - Polymer, organic photoelectronic device and display including the same - Google Patents

Abstract

According to the present invention, a polymer comprising a repeating unit represented by the following Chemical Formula 1 and including a functional group capable of crosslinking at its terminal can be provided.

[Formula 1]

Definitions of Ar ₁ , R ₁ , R ₂ , a and b in Chemical Formula 1 are as described in the detailed description of the invention.

In addition, the polymer according to the present invention can easily control the energy band gap, it is possible to provide an organic photoelectric device excellent in life and efficiency characteristics.

Crosslinking, high polymer, life span, efficiency, organic photoelectric device

Description

Polymer polymer, organic photoelectric device including the same, and display device including the same {Polymer, organic photoelectronic device and display including the same}

The present invention relates to a polymer polymer, an organic photoelectric device including the same, and a display device including the same, which can easily control an energy band gap and provide an organic photoelectric device having excellent life and efficiency characteristics.

An organic photoelectric device means a device that converts light energy into electrical energy in a broad sense, or vice versa. Among such organic photoelectric devices, organic light emitting diodes (OLEDs), in particular, have attracted attention as the demand for flat panel displays increases.

The organic electroluminescent device has a structure in which a functional organic thin film layer is inserted between an anode and a cathode. In this case, the organic thin film layer may include a light emitting layer, a hole injection layer, a hole transport layer, an electron transport layer, an electron injection layer, and the like, and may further include an electron blocking layer or a hole blocking layer due to light emission characteristics of the light emitting layer.

In general, the organic electroluminescent device has been widely used as a patterning technology vacuum deposition method using a fine metal mask (Fine Metal Mask). However, this vacuum deposition method was difficult to apply to large displays due to high process price and technical limitations. Accordingly, various patterning techniques that can replace the vacuum deposition method is being researched and developed. In particular, wet processes such as spin coating, inkjet printing, casting methods, etc. do not require vacuum technology, thereby reducing equipment costs, and easily fabricating devices without material loss.

However, wet process materials are not yet capable of achieving excellent device performance compared to vacuum deposition materials. In addition, when the organic thin film layer is formed by a wet process, a problem may occur in that the material of the lower layer that is already formed is melted by the organic solvent, and due to such a problem, it is difficult to stack the organic thin film layer in multiple layers and thus, excellent device performance cannot be realized. to be.

For example, the hydrophilic poly (3,4-ethylene dioxythiophene) / poly (4-styrenesulfonate) (PEDOT / PSS) layer used in a wet process is commonly used as a hole injection layer, but the hydrophilic hole The injection layer may be stacked together with the hydrophobic light emitting layer, which may cause a problem of poor interface characteristics. In addition, since the intrinsic material property of PEDOT / PSS is acidic, there is a problem such that the light emitting efficiency and lifespan of the device are degraded by damaging the cathode and the light emitting layer with time.

In order to solve the above problems, a polymer material is mainly used as a wet process material. These polymer materials are formed in such a way that an aromatic substituent such as an aryl group or an arylamine group is extended by a covalent bond. In general, as the molecular length increases, the airspace length increases, in which case the energy bandgap of the molecule decreases. Although polymer materials are synthesized with various polymer materials having different energy band gaps according to the degree of polymerization, and polymer materials having various molecular weight distributions are synthesized in one reactor, the polymer material is used to have a specific energy band gap. It is very difficult to obtain a thin film layer.

Therefore, in order to provide an organic photoelectric device having excellent life and efficiency characteristics by using a wet process, which is easy to manufacture the device and has advantages in terms of size and size, the interface stability between the organic thin film layers and the energy band gap are excellent. The development of a new polymer that can easily control the situation is required.

One embodiment of the present invention provides a polymer polymer having excellent interfacial stability between organic thin film layers and easy control of energy band gap.

Another embodiment of the present invention provides an organic photoelectric device having excellent life and efficiency characteristics, including the polymer.

Another embodiment of the present invention provides a display device including the organic photoelectric device.

Technical problems to be achieved by the present invention are not limited to the technical problems mentioned above, and other technical problems not mentioned will be clearly understood by those skilled in the art from the following description.

One embodiment of the present invention provides a polymer polymer including a repeating unit represented by the following Chemical Formula 1 and including a functional group capable of crosslinking at the terminal.

[Formula 1]

(In Chemical Formula 1)

Ar ₁ is a divalent organic group, a substituted or unsubstituted heteroalkylene group having 1 to 60 carbon atoms containing nitrogen, a substituted or unsubstituted heteroarylene group having 3 to 60 carbon atoms containing nitrogen, and having 6 to 60 carbon atoms. It is selected from the group consisting of a substituted or unsubstituted arylamine group,

R ₁ and R ₂ are the same as or different from each other, and are each independently selected from the group consisting of hydrogen, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 30 carbon atoms,

a and b are the same as or different from each other, and each independently, 0 or an integer between 1 and 4.)

Another embodiment of the present invention is an organic photoelectric device comprising an anode, a cathode and at least one organic thin film layer interposed between the anode and the cathode, at least one of the organic thin film layer is an embodiment of the present invention It provides an organic photoelectric device comprising a polymer according to the.

Another embodiment of the present invention provides a display device including the organic photoelectric device.

Other specific details of embodiments of the present invention are included in the following detailed description.

The polymer according to one embodiment of the present invention can synthesize a polymer material having a desired energy band gap without affecting the degree of polymerization of the polymer. In addition, by producing a polymer polymer so as to include a crosslinking group at the terminal, the formed organic thin film layer can form crosslinking to enhance the interfacial stability of the film.

In addition, the polymer polymer is excellent in the hole injection and movement characteristics, and has an effect of improving the performance of the organic photoelectric device by having an appropriate energy band gap that can be stepped energy level between the organic thin film layer. In addition, by solving the problem of dissolution or erosion of the other organic thin film layer by the solvent according to the wet process using the polymer polymer with improved interfacial stability, it is possible to provide an organic photoelectric device excellent in life and efficiency characteristics.

Hereinafter, embodiments of the present invention will be described in detail. However, this is presented as an example, by which the present invention is not limited, and the present invention is defined only by the scope of the claims to be described later.

In the present specification, "substituted" means unless otherwise defined, an alkyl group of 1 to 60 carbon atoms, an alkenyl group of 1 to 60 carbon atoms, a cycloalkyl group of 3 to 60 carbon atoms, a heterocycloalkyl group of 1 to 60 carbon atoms, 6 carbon atoms It means substituted with a substituent selected from the group consisting of an aryl group having from 60 to 60, a heteroaryl group having 3 to 60 carbon atoms, and an arylamine group having 6 to 60 carbon atoms.

In addition, in this specification, "hetero" means containing one to three heteroatoms of N, O, S, Si, or P in one ring, unless otherwise defined, and the remainder is carbon.

One embodiment of the present invention provides a polymer polymer including a repeating unit represented by the following Chemical Formula 1 and including a functional group capable of crosslinking at the terminal.

[Formula 1]

(In Chemical Formula 1)

Ar ₁ is a divalent organic group, a substituted or unsubstituted heteroalkylene group having 1 to 60 carbon atoms containing nitrogen, a substituted or unsubstituted heteroarylene group having 3 to 60 carbon atoms containing nitrogen, and having 6 to 60 carbon atoms. It is selected from the group consisting of a substituted or unsubstituted arylamine group,

R ₁ and R ₂ are the same as or different from each other, and are each independently selected from the group consisting of hydrogen, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 30 carbon atoms,

a and b are the same as or different from each other, and each independently, 0 or an integer between 1 and 4.)

When a is an integer of 2 or more, each R ₁ may be different, and when b is an integer of 2 or more, each R ₂ may be different.

In the case of the conventional polymer, it has a structure in which repeating units are connected to the positions of R ₁ and R ₂ . Such polymers have a proportional increase in the conjugation length between repeat units as the degree of polymerization increases. In general, high molecular weight polymers have various molecular weights, and thus have a molecular weight distribution. Accordingly, even polymer polymers synthesized by the same reaction have various energy levels and energy band gaps. Therefore, when the polymer is applied to the organic photoelectric device, there is a problem in that the device performance is deteriorated due to the energy level distribution and the energy band gap distribution.

In order to solve this problem, the present invention provides a polymer comprising a repeating unit represented by the formula (1) and comprising a functional group capable of crosslinking at the terminal. The polymer conjugate has an advantage in material design in which the conjugate length is controlled by Ar ₁ and the degree of polymerization does not increase even if the polymer chain increases. Therefore, it is possible to synthesize a polymer having a desired difference between a desired occupied molecular orbital (HOMO) and a lower unoccupied molecular orbital (LUMO), that is, a desired energy band gap. In addition, the interfacial stability of the film can be enhanced by synthesizing the material so as to include a crosslinking group at the terminal and forming the crosslinked organic thin film layer.

In addition, Ar ₁ of the polymer may introduce a fusion ring of aryl and heterocycloalkyl, such as a derivative of benzimidazole, into a substituent to improve electron transport characteristics. In addition, a fusion ring of an arylamine such as a carbazole group may be introduced as a substituent to improve hole transport characteristics.

More specifically, Ar ₁ of the polymer may be selected from the group consisting of substituents represented by the following Chemical Formulas 2 to 5.

[Formula 2]

(3)

[Formula 4]

[Chemical Formula 5]

(In Chemical Formulas 2 to 5,

Ar ₁₁ to Ar ₁₅ are the same as or different from each other, and each independently hydrogen, a halogen group, a cyano group, a hydroxy group, an amino group, a nitro group, a carboxyl group, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted carbon number Alkenyl groups of 1 to 50, substituted or unsubstituted cycloalkyl groups of 3 to 50 carbon atoms, substituted or unsubstituted heterocycloalkyl groups of 1 to 50 carbon atoms, substituted or unsubstituted aryl groups of 6 to 50 carbon atoms, substituted or unsubstituted A substituted C3-C50 heteroaryl group, a substituted or unsubstituted C6-C50 arylamine group, a substituted or unsubstituted C1-C50 alkoxy group, a substituted or unsubstituted C6-C50 aryl jade A heteroaryloxy group having 2 to 50 carbon atoms, a substituted or unsubstituted silyloxy group having 3 to 50 carbon atoms, a substituted or unsubstituted carbon group having 1 to 50 carbon atoms Real groups, substituted or unsubstituted alkoxycarbonyl groups having 2 to 50 carbon atoms, substituted or unsubstituted acyloxy groups having 2 to 50 carbon atoms, substituted or unsubstituted acylamino groups having 2 to 50 carbon atoms, substituted or unsubstituted carbon atoms 2 to 50 50 alkoxycarbonylamino group, substituted or unsubstituted aryloxycarbonylamino group having 7 to 50 carbon atoms, substituted or unsubstituted sulfamoylamino group having 1 to 50 carbon atoms, substituted or unsubstituted sulfonyl group having 1 to 50 carbon atoms, Substituted or unsubstituted C1-C50 alkylthiol group, substituted or unsubstituted C6-C50 arylthiol group, substituted or unsubstituted C1-C50 heterocycloalkylthiol group, substituted or unsubstituted C1-C50 1 to 50 ureide groups, substituted or unsubstituted C1-C50 phosphate groups, substituted or unsubstituted C3-C50 silyl groups, and their melting Will be selected from the group consisting of ring,

e, f, g, h, i, j, k, and l are the same or different from each other and are each independently an integer between 0 or 1-4.)

Ar ₁₁ to Ar ₁₅ in Formulas 2 to 5 are the same as or different from each other, a substituted or unsubstituted cycloalkyl group having 3 to 50 carbon atoms, a substituted or unsubstituted heterocycloalkyl group having 1 to 50 carbon atoms, substituted or An 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 arylamine group having 6 to 50 carbon atoms, and a fusion ring thereof In this case, the effect of improving the electron and hole transport characteristics can be obtained, which is better.

In particular, the aryl in the formula 2 to 5 is monocyclic aryl such as phenyl, biphenyl, terphenyl, styrene; Alternatively, polycyclic aryl such as naphthyl, anthracenyl, phenanthrenyl, pyrenyl, peryllenyl, pyrenyl, and fluorenyl may be used as a light emitting layer of an organic photoelectric device.

More specifically, the repeating unit represented by Chemical Formula 1 may be used including a repeating unit represented by the following Chemical Formulas 6 to 18.

[Formula 6]

[Formula 7]

[Formula 8]

[Chemical Formula 9]

[Formula 10]

[Formula 11]

[Chemical Formula 12]

[Chemical Formula 13]

[Formula 14]

[Formula 15]

[Chemical Formula 16]

[Chemical Formula 17]

[Chemical Formula 18]

In addition, the polymer according to the embodiment of the present invention more preferably uses a polymer having a weight average molecular weight of 15,000 or more.

The polymer according to the embodiment of the present invention includes a functional group capable of crosslinking at the terminal, thereby forming crosslinking of the organic thin film layer to enhance interfacial stability of the film. In addition, by solving the problem of dissolution or erosion of the other organic thin film layer by the solvent according to the wet process using the polymer polymer with improved interfacial stability, it is possible to provide an organic photoelectric device excellent in life and efficiency characteristics.

The crosslinking may be applied to crosslinks according to various crosslinking reactions such as thermal curing and photocuring.

The crosslinkable functional group is generally used in the art, and is not particularly limited. For example, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted (meth) acryl group, a substituted or unsubstituted epoxy group, A functional group including a substituent selected from the group consisting of a substituted or unsubstituted styrene group and a substituted or unsubstituted alkoxy group can be used. In this case, the "substituted" is preferably an alkyl group having 1 to 10 carbon atoms or an aryl group having 6 to 30 carbon atoms.

The polymer according to the embodiment of the present invention has a difference between a homogestive occupied molecular orbital (HOMO) and a lower unoccupied molecular orbital (LUMO) of 2.4 eV or more, and is composed of a repeating unit having excellent hole injection and migration characteristics, and thus an organic electric It can be very usefully applied to the hole injection and transport layer of the light emitting device. In particular, the energy band gap is large enough to improve the lifetime and efficiency characteristics of the device when applied to an organic photoelectric device.

Another embodiment of the present invention is an organic photoelectric device comprising an anode, a cathode and at least one organic thin film layer interposed between the anode and the cathode, at least one of the organic thin film layer is an embodiment of the present invention It provides an organic photoelectric device comprising a polymer according to the. In this case, the organic photoelectric device means an organic light emitting device, an organic solar cell, an organic transistor, an organic photosensitive drum, or an organic memory device. In particular, in the case of an organic solar cell, a polymer polymer according to an embodiment of the present invention is included in an electrode or an electrode buffer layer to increase quantum efficiency, and in the case of an organic transistor, the polymer may be used as an electrode material in a gate or a source-drain electrode. .

In particular, the organic photoelectric device according to the embodiment of the present invention is preferably a phosphorescent organic light emitting device. The phosphorescent organic light emitting device refers to a device including a material that emits phosphorescence in the light emitting layer, and the phosphorescent material includes a metal complex capable of emitting light by multiplet excitaion in a triplet state or more. It is advisable to use substances that contain it. More specific examples of the phosphorescent light emitting material include an organometallic compound including an element selected from the group consisting of Ir, Pt, Os, Ti, Zr, Hf, Eu, Tb, Tm, and combinations thereof, or oligomer to polymer materials including the same. Can be used. More specifically, as the red phosphorescent dopant, platinum-octaethylporphyrin complex (PtOEP), Ir (Piq) ₂ (acac), Ir (Piq) _3, etc. may be used, and as the green phosphorescent dopant, Ir (PPy) _{2 is used.} (acac), Ir (PPy) ₃ and the like can be used, and as the blue phosphorescent dopant, (4,6-F ₂ PPy) ₂ Irpic or the like can be used. At this time, Piq means 1-phenylisoquinoline (1-phenylisoquinoline), acac means acetylacetonate, F ₂ PPy means 2- (difluorophenyl) pyridinato, pic is Refers to picolinate, PPy means 2-phenylpyridine.

The polymer according to one embodiment of the present invention can be used as a host material or a charge transport material.

In addition, the organic thin film layer which may include the polymer may include a layer selected from the group consisting of a light emitting layer, a hole transport layer, a hole injection layer, a hole blocking layer, an electron transport layer, an electron injection layer, an electron blocking layer, and a combination thereof. At least one of the layers may include a polymer according to an embodiment of the present invention.

Hereinafter, the organic photoelectric device according to the embodiment of the present invention will be described in detail.

1 to 5 are cross-sectional views of an organic photoelectric device including a polymer according to an embodiment of the present invention.

1 to 5, an organic photoelectric device 100, 200, 300, 400, and 500 according to an embodiment of the present invention may include an anode 120, a cathode 110, and a gap between the anode and the cathode. It has a structure including at least one organic thin film layer 105 interposed therebetween.

The anode 120 includes a cathode material, and a material having a large work function is preferable as the anode material so that hole injection can be smoothly injected into the organic thin film layer. Specific examples of the positive electrode material include metals such as nickel, platinum, vanadium, chromium, copper, zinc, and gold or alloys thereof, and include zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO). Metal oxides such as ZnO and Al or SnO ₂

And combinations of metals and oxides such as Sb, poly (3-methylthiophene), poly [3,4- (ethylene-1,2-dioxy) thiophene] (polyehtylenedioxythiophene: PEDT), polypyrrole and And conductive polymers such as polyaniline. However, the positive electrode material is not limited to these compounds. In particular, it is preferable to use a transparent electrode containing ITO as the anode material.

The negative electrode 110 includes a negative electrode material, and the negative electrode material is preferably a material having a small work function to facilitate electron injection into the organic thin film layer. Specific examples of the negative electrode material include metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin, lead, cesium, barium, or alloys thereof, and LiF / Al. And multilayered structure materials such as LiO ₂ / Al, LiF / Ca, LiF / Al, and BaF ₂ / Ca. However, the negative electrode material is not limited to these compounds. In particular, it is preferable to use a metal electrode such as aluminum as the cathode material.

First, referring to FIG. 1, FIG. 1 illustrates an organic photoelectric device 100 in which only a light emitting layer 130 exists as an organic thin film layer 105. The organic thin film layer 105 may exist only as a light emitting layer 130.

Referring to FIG. 2, FIG. 2 illustrates a two-layered organic photoelectric device 200 in which an emission layer 230 including an electron transport layer and a hole transport layer 140 exist as an organic thin film layer 105, and an organic thin film layer 105. The silver may have a two-layer type including an emission layer 230 and a hole transport layer 140. In this case, the light emitting layer 130 functions as an electron transporting layer, and the hole transporting layer 140 functions to improve bonding and hole transporting properties with a transparent electrode such as ITO.

Referring to FIG. 3, FIG. 3 illustrates a three-layered organic photoelectric device 300 having an electron transport layer 150, a light emitting layer 130, and a hole transport layer 140 as an organic thin film layer 105. In 105, the light emitting layer 130 is in an independent form, and has a form in which layers (electron transport layer 150 and hole transport layer 140) having excellent electron transport properties and hole transport properties are stacked in separate layers.

Referring to FIG. 4, FIG. 4 illustrates a four-layered organic photoelectric device including an electron injection layer 160, an emission layer 130, a hole transport layer 140, and a hole injection layer 170 as an organic thin film layer 105. As shown in FIG. 4, the hole injection layer 170 may improve adhesion to ITO used as an anode.

Referring to FIG. 5, FIG. 5 is an organic thin film layer 105, which is different from an electron injection layer 160, an electron transport layer 150, an emission layer 130, a hole transport layer 140, and a hole injection layer 170. As a five-layered organic photoelectric device 500 having five layers serving as a function, the organic photoelectric device 500 is effective in lowering voltage by separately forming an electron injection layer 160.

1 to 5, the electron transport layer 150, the electron injection layer 160, the light emitting layers 130 and 230, the hole transport layer 140, and the hole injection layer 170 forming the organic thin film layer 105, or these Combinations of the above polymers. In this case, the polymer may be used in the electron transport layer 150 including the electron transport layer 150 or the electron injection layer 160, and in particular, when included in the electron transport layer, a hole blocking layer (not shown) is separately provided. Since there is no need to form, it is possible to provide an organic photoelectric device of a simplified structure is effective.

The above-described organic photoelectric device includes a dry film method such as vacuum deposition, sputtering, plasma plating, and ion plating after an anode is formed on a substrate; Alternatively, the organic thin film layer may be formed by a wet film method such as spin coating, dipping, flow coating, or the like, followed by forming a cathode thereon.

In particular, the polymer according to an embodiment of the present invention can be more usefully applied to large display devices by forming an organic thin film layer by a wet film method. In particular, the polymer of the present invention can enhance the interfacial stability of the film by forming the cross-linked organic thin film layer. By solving the problem of dissolving or eroding the other organic thin film layer by the solvent according to the wet process using the polymer polymer with improved interface stability, it is possible to provide an organic photoelectric device excellent in life and efficiency characteristics.

According to another embodiment of the present invention, a display device including the organic photoelectric device is provided.

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.

Example 1 Synthesis of Polymer Polymer (1)

The polymer polymer (1) of the present invention was synthesized through the following two steps.

First Step: Synthesis of Monomer (1)

[Reaction Scheme 1]

2.223 g (10 mmol) of isobutylcarbazole, 4.82 g (20 mmol) of tris (4-bromophenyl) amine, and 0.3 g (3 mmol) of cuprous chloride and 4.15 g (30 mmol) of potassium carbonate in a nitrogen atmosphere Suspended in 40 ml of sulfoxide (DMSO) and heated to reflux for 4 hours. After the reaction was completed, the reaction was cooled to room temperature and extracted several times with ethyl acetate and water. Thereafter, water was removed with anhydrous magnesium sulfate, and then filtered and the solvent was removed under reduced pressure.

The obtained product was purified by gas chromatography (silica gel column, GPC) to obtain 2.4 g (yield: 32%) of monomer (2). The synthesized monomer (1) was confirmed by measuring ¹ H-NMR using a Bruker 300 MHz.

¹ H-NMR (CDCl ₃ , ppm): δ 0.92 (doublet, 6H), 1.93 (multiplet, 1H), 2.61 (doublet, 2H), 7.08 (multiplet, 5H), 7.25 (multiplet, 4H), 7.40 (multiplet , 8H), 8.02 (doublet, 1H), 8.10 (doublet, 1H)

Second Step: Synthesis of Polymer Polymer (1)

Scheme 2

0.624 g (1 mmol) of monomer (1) obtained in step 1 above under a nitrogen atmosphere, 0.584 g (1 mmol) of fluorene boronic acid-pinacholate, 6 mg (0.005 mmol) of tetrakis- (triphenylphosphine) palladium, tetra 10 ml of ethylammonium hydroxide aqueous solution, 10 ml of toluene, and 10 ml of THF were mixed and stirred at 100 ° C for 8 hours.

After the temperature was lowered to 80 ° C., 0.183 g of 4-bromostyrene was added to the mixed solution and stirred for 2 hours, and then 0.2 g of 4-styrene boronic acid was added and stirred for 4 hours. The reaction was precipitated in 200 ml of methanol to precipitate a high polymer. The precipitated polymer was dissolved in 50 ml of toluene, and then reprecipitated in 300 ml of acetone: ethanol: water (1: 1: 1 volume ratio). The precipitated polymer was filtered and then dissolved in toluene and purified by Florisil column chromatography. This obtained 1 g of yellow high polymers (1). The number average molecular weight (Mn) of the high polymer (1) is 18000.

The styrene group (crosslinking group) attached to the end of the polymer (1) was confirmed by ¹ H-NMR (CDCl ₃ , ppm) and is shown in FIG. 6. Referring to FIG. 6, it was confirmed that a proton peak was observed at a typical position of the ethylene group of the styrene group (5.3 ppm: 5.7 ppm: 6.7 ppm = 1: 1).

Example 2: Synthesis of Polymer Polymer (2)

The polymer (2) used two monomers used in the polymer (1) of Example 1 and synthesized by changing the end group reaction in order to increase the number of styrene groups of the end group.

Scheme 3

0.624 g (1 mmol) of monomer (1) obtained in step 1 of Example 1 above in a nitrogen atmosphere, 0.584 g (1 mmol) of fluorene boronic acid-pinacolate, and 6 mg (0.005) of tetrakis- (triphenylphosphine) palladium mmol), 10 ml of tetraethylammonium hydroxide aqueous solution, 10 ml of toluene, and 10 ml of THF were mixed and stirred at 100 ° C for 8 hours.

After the temperature was lowered to 80 ° C., 0.315 g of 1,3,5-tribromobenzene was added to the mixed solution and stirred for 2 hours, followed by 0.6 g of 4-styrene boronic acid, followed by stirring for 4 hours. The reaction was precipitated in 200 ml of methanol to precipitate a high polymer. The precipitated polymer was dissolved in 50 ml of toluene, and then reprecipitated in 300 ml of acetone: ethanol: water (1: 1: 1 volume ratio). The precipitated polymer was filtered, dissolved in toluene, and purified by Florisil column chromatography. This obtained 0.8 g of yellow high polymers (2). The number average molecular weight (Mn) of the high polymer (2) is 20000.

Example 3: Synthesis of Polymer Polymer (3)

The high polymer (3) is 3,5-dibromo-N, N-dip-tolylbenzeneamine (3,5-dibromo-N, N-dip-tolylbenzenamine) in place of the monomer (1) of Example 1 Synthesis was carried out in the same manner as in the synthesis of Polymer Polymer (1) of Example 1, except that was used as the monomer.

Scheme 4

0.431 g (1 mmol) of 3,5-dibromo-N, N-dip-tolylbenzenamine (3,5-dibromo-N, N-dip-tolylbenzenamine) in a nitrogen atmosphere, fluoreneboronic acid-pinacholate 0.584 g (1 mmol), 6 mg (0.005 mmol) of tetrakis- (triphenylphosphine) palladium, 10 ml of tetraethylammonium hydroxide aqueous solution, 10 ml of toluene, and 10 ml of THF were mixed for 8 hours at 100 ° C. Stirred.

After the temperature was lowered to 80 ° C., 0.183 g of 4-bromostyrene was added to the mixed solution and stirred for 2 hours, and then 0.2 g of 4-styrene boronic acid was added and stirred for 4 hours. The reaction was precipitated in 200 ml of methanol to precipitate a high polymer. The precipitated polymer was dissolved in 50 ml of toluene, and then reprecipitated in 300 ml of acetone: ethanol: water (1: 1: 1 volume ratio). The precipitated polymer was filtered and then dissolved in toluene and purified by Florisil column chromatography. This obtained 1 g of yellow high polymers (3). The number average molecular weight (Mn) of the high molecular polymer (3) is 17000.

Example 4 Synthesis of Polymer Polymer (4)

The polymer (4) is 3,5-dibromo-N, N-dip-tolylbenzeneamine (3,5-dibromo-N, N-dip-tolylbenzenamine) in place of the monomer (1) of Example 1 Synthesis was carried out in the same manner as in the synthesis of Polymer Polymer (2) of Example 2, except that was used as the monomer.

Scheme 5

0.431 g (1 mmol) of 3,5-dibromo-N, N-dip- tolylbenzenamine (3,5-dibromo-N, N-dip-tolylbenzeneamine) in a nitrogen atmosphere, fluoreneboronic acid-pinacholate 0.584 g (1 mmol), 6 mg (0.005 mmol) of tetrakis- (triphenylphosphine) palladium, 10 ml of tetraethylammonium hydroxide aqueous solution, 10 ml of toluene, and 10 ml of THF were mixed for 8 hours at 100 ° C. Stirred.

After the temperature was lowered to 80 ° C., 0.315 g of 1,3,5-tribromobenzene was added to the mixed solution and stirred for 2 hours, followed by 0.6 g of 4-styrene boronic acid, followed by stirring for 4 hours. The reaction was precipitated in 200 ml of methanol to precipitate a high polymer. The precipitated polymer was dissolved in 50 ml of toluene, and then reprecipitated in 300 ml of acetone: ethanol: water (1: 1: 1 volume ratio). The precipitated polymer was filtered, dissolved in toluene, and purified by Florisil column chromatography. This obtained 0.8 g of yellow high polymers (4). The number average molecular weight (Mn) of the high polymer (4) is 24000.

Experimental Example 1 Analysis of Luminescence Characteristics

The spectral characteristics (UV / Visible absorption and photoluminescence emission) of the polymer synthesized in Examples 1 to 4 were measured under the following conditions.

A solution of 10 mg of polymer dissolved in 1 mL of toluene was filtered through a 0.45 μm PTFE syringe membrane, and 0.2 ml of the filtrate was spin-coated on a quartz substrate (2 cm ㅧ 2 cm) at a speed of 2000 rpm, followed by 10 at 80 ° C. Drying for a minute gave a thin film of 20 nm thickness.

UV / Visible absorption and photoluminescence emission wavelengths of the polymer coated on the substrate were measured using a UV Spectrometer (Shimadzu, UV-1650 PC) and a Spectroradiometer (Minolta, CS-1000A) at room temperature (about 25 ° C.), The PL (photoluminescence) emission wavelength of the solution at 77 K was measured. At this time, the spectroscopic characteristics of the polymer according to Examples 1 to 3 are shown in Figs.

As a result, the triplet energy band gap could be calculated, and in particular, the triplet energy band gap of the polymer according to Example 3 was confirmed to be 2.7 eV.

Experimental Example 2: Analysis of Membrane Properties

10 mg of the polymer according to Example 3 was dissolved in 1 mL of xylene. After filtration with a 45 μm PTFE syringe membrane, a membrane was formed by spin coating the glass substrate at a speed of 2000 rpm. The formed membrane was dried at 180 ° C. for 60 minutes, and then molecular weight was confirmed by gas phase chromatography (GPC). The number average molecular weight (Mn) after the film was formed was 47,000, which was 2.7 times increased compared with 17,000 before curing.

As a result, when the polymer according to Example 3 was used as the organic thin film layer of the organic photoelectric device, it was confirmed that the interfacial stability of the film could be enhanced by forming crosslinks.

Example 5 Fabrication of Organic Light Emitting Diode

An organic light emitting diode comprising the polymer according to Example 3 was manufactured in the following device structure.

An ITO substrate was used as the cathode, and a PEDOT: PSS film was formed to a thickness of 60 nm by spin coating on the substrate. The PEDOT: PSS membrane was dried at 180 ° C. for 20 minutes, and was then formed by spin coating a polymer polymer according to Example 3 to a thickness of 20 nm on the PEDOT: PSS membrane, and dried at 180 ° C. for 60 minutes.

A light emitting layer was formed to a thickness of 40 nm on the upper layer of the film including the polymer according to Example 3 by spin coating. 4,4 ', 4 "-tri (N-carbazolyl) triphenylamine: 2-tert-butylphenyl-5-biphenyl-1,3,4'-oxadiazole (TCTA: PBD = 1: 1) The mixture was used as a host and the Ir (PPy) ₂ (acac) dopant was doped at 5% by weight of the total amount of the light emitting layer to form a light emitting layer, which was dried at 110 ° C. for 10 minutes.

BAlq was vacuum deposited on the light emitting layer to form a hole blocking layer having a thickness of 5 nm. Thereafter, Alq was vacuum-deposited on the emission layer to form an electron transport layer having a thickness of 20 nm.

An organic light emitting device was manufactured by forming an anode by sequentially vacuum depositing LiF 1 nm and Al 100 nm on the electron transport layer.

Comparative Example 1

An organic light emitting device that does not contain the polymer according to Example 3 was manufactured in the following device structure.

An ITO substrate was used as the cathode, and a PEDOT: PSS film was formed to a thickness of 60 nm by spin coating on the substrate. The PEDOT: PSS membrane was dried at 180 ° C. for 20 minutes.

A light emitting layer was formed to a thickness of 40 nm on the upper layer of the PEDOT: PSS film by spin coating. 4,4 ', 4 "-tri (N-carbazolyl) triphenylamine: 2-tert-butylphenyl-5-biphenyl-1,3,4'-oxadiazole (TCTA: PBD = 1: 1) The mixture was used as a host and the Ir (PPy) ₂ (acac) dopant was doped at 5% by weight of the total amount of the light emitting layer to form a light emitting layer, which was dried at 110 ° C. for 10 minutes.

BAlq was vacuum deposited on the light emitting layer to form a hole blocking layer having a thickness of 5 nm. Thereafter, Alq was vacuum-deposited on the emission layer to form an electron transport layer having a thickness of 20 nm.

An organic light emitting device was manufactured by forming an anode by sequentially vacuum depositing LiF 1 nm and Al 100 nm on the electron transport layer.

Experimental Example 3: Evaluation of Characteristics of Organic Light-Emitting Device

1) Measurement of driving voltage, luminance, and luminous efficiency

For the organic light emitting diodes of Example 5 and Comparative Example 1, the driving voltage (V) required to produce a brightness of 2000 cd / cm ² was measured, and the current efficiency (cd / A) and power efficiency (lm / W) of the same brightness were measured. ) Is shown in Table 1. In addition, the voltage at the instant when the organic light emitting element starts to emit light is shown in Table 1 below as a turn-on voltage.

2) Luminance change according to the change of current density

The current value flowing through the unit device was measured using a current-voltmeter (Keithley 2400), and the current density was measured by dividing the measured current value by the area of the organic light emitting device. The latitude change according to the change of the current density of the organic light emitting diodes of Example 5 and Comparative Example 1 was measured and shown in FIG. 10.

3) Change in current efficiency according to the change in brightness

The luminance was measured using a luminance meter (Minolta Cs-1000A), and the change in current efficiency according to the change in luminance of the organic light emitting diodes of Example 5 and Comparative Example 1 was measured and shown in FIG. 11.

[Table 1]

Turn-on voltage Luminance luminance at 2000 cd / cm ² Driving voltage Current efficiency Power efficiency Color coordinates Comparative Example 1 6.4 V 11.5V 12.5cd / A 3.4 lm / W 0.29, 0.60 Example 5 6.0V 10.6V 24.2cd / A 7.2 lm / W 0.30, 0.61

Compared to the organic light emitting diode according to Comparative Example 1 that does not include the polymer, the organic light emitting diode according to Example 5 has an effect of reducing driving voltage, improving current efficiency by 94%, and improving power efficiency by 112%. I could confirm that.

The present invention is not limited to the above embodiments, but may be manufactured in various forms, and a person skilled in the art to which the present invention pertains has another specific form without changing the technical spirit or essential features of the present invention. It will be appreciated that the present invention may be practiced as. It is therefore to be understood that the above-described embodiments are illustrative in all aspects and not restrictive.

1 to 5 are cross-sectional views illustrating various embodiments of an organic photoelectric device that may be manufactured including a polymer according to an embodiment of the present invention.

6 is 1 for the polymer 1 according to Example ¹

H-NMR spectrum is shown.

FIG. 7 is a graph showing the results of measuring UV / Visible absorption and PL (photoluminescence) emission wavelengths of the polymer synthesized in Example 1. FIG.

8 is a graph showing the results of measuring UV / Visible absorption and PL (photoluminescence) emission wavelengths for the polymer synthesized in Example 2. FIG.

9 is a graph showing the results of measuring UV / Visible absorption and PL (photoluminescence) emission wavelengths for the polymer synthesized in Example 3. FIG.

FIG. 10 is a graph illustrating measurement of luminance change according to a change in current density of the organic light emitting diodes of Example 5 and Comparative Example 1. FIG.

FIG. 11 illustrates changes in current efficiency according to changes in luminance with respect to organic light emitting diodes of Example 5 and Comparative Example 1. FIG.

<Explanation of symbols for the main parts of the drawings>

100: organic photoelectric device 110: cathode

120: anode 105: organic thin film layer

130: light emitting layer 140: hole transport layer

150: electron transport layer 160: electron injection layer

170: hole injection layer 230: light emitting layer + electron transport layer

Claims (8)

A polymer comprising a repeating unit represented by the following formula (1) and comprising a functional group capable of crosslinking at the terminal: [Formula 1]

(In the formula 1, Ar ₁ is a divalent organic group, a substituted or unsubstituted heteroalkylene group having 1 to 60 carbon atoms containing nitrogen, a substituted or unsubstituted heteroarylene group having 3 to 60 carbon atoms containing nitrogen, and having 6 to 60 carbon atoms. It is selected from the group consisting of a substituted or unsubstituted arylamine group, R ₁ and R ₂ are the same as or different from each other, and are each independently selected from the group consisting of hydrogen, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, a and b are the same as or different from each other, and each independently, 0 or an integer between 1 and 4.) The method of claim 1, Ar ₁ of the polymer Is a polymer polymer selected from the group consisting of substituents represented by the following Chemical Formulas 2 to 5: [Formula 2]

(3)

[Formula 4]

[Chemical Formula 5]

(In Chemical Formulas 2 to 5, Ar ₁₁ to Ar ₁₅ are the same as or different from each other, and each independently hydrogen, a halogen group, a cyano group, a hydroxy group, an amino group, a nitro group, a carboxyl group, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted carbon number Alkenyl groups of 1 to 50, substituted or unsubstituted cycloalkyl groups of 3 to 50 carbon atoms, substituted or unsubstituted heterocycloalkyl groups of 1 to 50 carbon atoms, substituted or unsubstituted aryl groups of 6 to 50 carbon atoms, substituted or unsubstituted A substituted C3-C50 heteroaryl group, a substituted or unsubstituted C6-C50 arylamine group, a substituted or unsubstituted C1-C50 alkoxy group, a substituted or unsubstituted C6-C50 aryl jade A heteroaryloxy group having 2 to 50 carbon atoms, a substituted or unsubstituted silyloxy group having 3 to 50 carbon atoms, a substituted or unsubstituted carbon group having 1 to 50 carbon atoms Real groups, substituted or unsubstituted alkoxycarbonyl groups having 2 to 50 carbon atoms, substituted or unsubstituted acyloxy groups having 2 to 50 carbon atoms, substituted or unsubstituted acylamino groups having 2 to 50 carbon atoms, substituted or unsubstituted carbon atoms 2 to 50 50 alkoxycarbonylamino group, substituted or unsubstituted aryloxycarbonylamino group having 7 to 50 carbon atoms, substituted or unsubstituted sulfamoylamino group having 1 to 50 carbon atoms, substituted or unsubstituted sulfonyl group having 1 to 50 carbon atoms, Substituted or unsubstituted C1-C50 alkylthiol group, substituted or unsubstituted C6-C50 arylthiol group, substituted or unsubstituted C1-C50 heterocycloalkylthiol group, substituted or unsubstituted C1-C50 1 to 50 ureide groups, substituted or unsubstituted C1-C50 phosphate groups, substituted or unsubstituted C3-C50 silyl groups, and their melting Will be selected from the group consisting of ring, e, f, g, h, i, j, k, and l are the same or different from each other and independently of each other, 0 or an integer between 1 and 4). The method of claim 1, The crosslinkable functional group is a group consisting of a substituted or unsubstituted alkenyl group, a substituted or unsubstituted (meth) acryl group, a substituted or unsubstituted epoxy group, a substituted or unsubstituted styrene group, and a substituted or unsubstituted alkoxy group. A polymer comprising a substituent selected from. The method of claim 1, The polymer is a polymer of the difference between the HOMO (higest occupied molecular orbital) and LUMO (lowest unoccupied molecular orbital) is 2.4 eV or more. An anode, a cathode and at least one organic thin film layer interposed between the anode and the cathode, At least one of the organic thin film layer is an organic photoelectric device comprising the polymer polymer according to any one of claims 1 to 4. The method of claim 5, The polymer polymer is an organic photoelectric device that is used as a host material or a charge transport material. The method of claim 5, The organic thin film layer is an organic photoelectric device that is selected from the group consisting of a light emitting layer, a hole transport layer, a hole injection layer, a hole blocking layer, an electron transport layer, an electron injection layer, an electron blocking layer, and combinations thereof. A display device comprising the organic photoelectric device of claim 5.

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