KR102665292B1 - Novel compound and organic light emitting device comprising the same - Google Patents
Novel compound and organic light emitting device comprising the same Download PDFInfo
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- KR102665292B1 KR102665292B1 KR1020190010745A KR20190010745A KR102665292B1 KR 102665292 B1 KR102665292 B1 KR 102665292B1 KR 1020190010745 A KR1020190010745 A KR 1020190010745A KR 20190010745 A KR20190010745 A KR 20190010745A KR 102665292 B1 KR102665292 B1 KR 102665292B1
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- compound
- organic light
- layer
- emitting device
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- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 150000003413 spiro compounds Chemical class 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- JLBRGNFGBDNNSF-UHFFFAOYSA-N tert-butyl(dimethyl)borane Chemical group CB(C)C(C)(C)C JLBRGNFGBDNNSF-UHFFFAOYSA-N 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- IBBLKSWSCDAPIF-UHFFFAOYSA-N thiopyran Chemical compound S1C=CC=C=C1 IBBLKSWSCDAPIF-UHFFFAOYSA-N 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical compound [Al+3].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 TVIVIEFSHFOWTE-UHFFFAOYSA-K 0.000 description 1
- KWQNQSDKCINQQP-UHFFFAOYSA-K tri(quinolin-8-yloxy)gallane Chemical compound C1=CN=C2C(O[Ga](OC=3C4=NC=CC=C4C=CC=3)OC=3C4=NC=CC=C4C=CC=3)=CC=CC2=C1 KWQNQSDKCINQQP-UHFFFAOYSA-K 0.000 description 1
- LALRXNPLTWZJIJ-UHFFFAOYSA-N triethylborane Chemical group CCB(CC)CC LALRXNPLTWZJIJ-UHFFFAOYSA-N 0.000 description 1
- WXRGABKACDFXMG-UHFFFAOYSA-N trimethylborane Chemical group CB(C)C WXRGABKACDFXMG-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- MXSVLWZRHLXFKH-UHFFFAOYSA-N triphenylborane Chemical group C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 MXSVLWZRHLXFKH-UHFFFAOYSA-N 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
- HTPBWAPZAJWXKY-UHFFFAOYSA-L zinc;quinolin-8-olate Chemical compound [Zn+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 HTPBWAPZAJWXKY-UHFFFAOYSA-L 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/20—Polycyclic condensed hydrocarbons
- C07C15/27—Polycyclic condensed hydrocarbons containing three rings
- C07C15/28—Anthracenes
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
- C07C2603/24—Anthracenes; Hydrogenated anthracenes
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- Materials Engineering (AREA)
- Electroluminescent Light Sources (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
본 발명은 신규한 화합물 및 이를 이용한 유기발광 소자를 제공한다.The present invention provides a novel compound and an organic light-emitting device using the same.
Description
본 발명은 신규한 화합물 및 이를 포함하는 유기 발광 소자에 관한 것이다. The present invention relates to novel compounds and organic light-emitting devices containing them.
일반적으로 유기 발광 현상이란 유기 물질을 이용하여 전기에너지를 빛에너지로 전환시켜주는 현상을 말한다. 유기 발광 현상을 이용하는 유기 발광 소자는 넓은 시야각, 우수한 콘트라스트, 빠른 응답 시간을 가지며, 휘도, 구동 전압 및 응답 속도 특성이 우수하여 많은 연구가 진행되고 있다. In general, organic luminescence refers to a phenomenon that converts electrical energy into light energy using organic materials. Organic light-emitting devices using the organic light-emitting phenomenon have a wide viewing angle, excellent contrast, fast response time, and excellent luminance, driving voltage, and response speed characteristics, so much research is being conducted.
유기 발광 소자는 일반적으로 양극과 음극 및 상기 양극과 음극 사이에 유기물층을 포함하는 구조를 가진다. 상기 유기물층은 유기 발광 소자의 효율과 안정성을 높이기 위하여 각기 다른 물질로 구성된 다층의 구조로 이루어진 경우가 많으며, 예컨대 정공주입층, 정공수송층, 발광층, 전자수송층, 전자주입층 등으로 이루어질 수 있다. 이러한 유기 발광 소자의 구조에서 두 전극 사이에 전압을 걸어주게 되면 양극에서는 정공이, 음극에서는 전자가 유기물층에 주입되게 되고, 주입된 정공과 전자가 만났을 때 엑시톤(exciton)이 형성되며, 이 엑시톤이 다시 바닥상태로 떨어질 때 빛이 나게 된다. Organic light emitting devices generally have a structure including an anode, a cathode, and an organic material layer between the anode and the cathode. The organic material layer is often composed of a multi-layer structure made of different materials to increase the efficiency and stability of the organic light-emitting device, and may be composed of, for example, a hole injection layer, a hole transport layer, a light-emitting layer, an electron transport layer, and an electron injection layer. In the structure of this organic light-emitting device, when a voltage is applied between the two electrodes, holes are injected from the anode and electrons from the cathode into the organic material layer. When the injected holes and electrons meet, an exciton is formed, and this exciton When it falls back to the ground state, it glows.
상기와 같은 유기 발광 소자에 사용되는 유기물에 대하여 새로운 재료의 개발이 지속적으로 요구되고 있다.The development of new materials for organic materials used in organic light-emitting devices as described above is continuously required.
한편, 최근에는 공정 비용 절감을 위하여 기존의 증착 공정 대신 용액 공정, 특히 잉크젯 공정을 이용한 유기 발광 소자가 개발되고 있다. 초창기에는 모든 유기 발광 소자 층을 용액 공정으로 코팅하여 유기 발광 소자를 개발하려 하였으나 현재 기술로는 한계가 있어, 정구조 형태에서 HIL, HTL, EML만을 용액 공정으로 진행하고 추후 공정은 기존의 증착 공정을 활용하는 하이브리드(hybrid) 공정이 연구 중이다. Meanwhile, recently, in order to reduce process costs, organic light-emitting devices have been developed using a solution process, especially an inkjet process, instead of the existing deposition process. In the early days, attempts were made to develop organic light emitting devices by coating all organic light emitting device layers using a solution process, but there are limitations to the current technology, so only HIL, HTL, and EML in the form of a fixed structure were performed using a solution process, and the subsequent processes were carried out using the existing deposition process. A hybrid process utilizing is being studied.
이에 본 발명에서는 유기 발광 소자에 사용될 수 있으면서 동시에 용액 공정에 사용 가능한 신규한 유기 발광 소자의 소재를 제공한다.Accordingly, the present invention provides a novel organic light-emitting device material that can be used in an organic light-emitting device and at the same time can be used in a solution process.
본 발명은 신규한 화합물 및 이를 포함하는 유기 발광 소자에 관한 것이다. The present invention relates to novel compounds and organic light-emitting devices containing them.
본 발명은 하기 화학식 1로 표시되는 화합물을 제공한다:The present invention provides a compound represented by the following formula (1):
[화학식 1] [Formula 1]
상기 화학식 1에서,In Formula 1,
L1 및 L2는 각각 독립적으로, 단일결합; 치환 또는 비치환된 C6-60 아릴렌; 또는 치환 또는 비치환된 N, O 및 S로 구성되는 군으로부터 선택되는 어느 하나 이상을 포함하는 C2-60 헤테로아릴렌이고,L 1 and L 2 are each independently a single bond; Substituted or unsubstituted C 6-60 arylene; or a C 2-60 heteroarylene containing at least one selected from the group consisting of substituted or unsubstituted N, O and S,
Ar1 및 Ar2는 각각 독립적으로, 치환 또는 비치환된 C6-60 아릴; 또는 치환 또는 비치환된 N, O 및 S로 구성되는 군으로부터 선택되는 어느 하나 이상을 포함하는 C2-60 헤테로아릴이다. Ar 1 and Ar 2 are each independently substituted or unsubstituted C 6-60 aryl; or C 2-60 heteroaryl containing at least one selected from the group consisting of substituted or unsubstituted N, O, and S.
또한, 본 발명은 제1 전극; 상기 제1 전극과 대향하여 구비된 제2 전극; 및 상기 제1 전극과 상기 제2 전극 사이에 구비된 발광층을 포함하는 유기 발광 소자로서, 상기 발광층은 상기 화학식 1로 표시되는 화합물을 포함하는, 유기 발광 소자를 제공한다.In addition, the present invention includes a first electrode; a second electrode provided opposite to the first electrode; and an organic light-emitting device comprising a light-emitting layer provided between the first electrode and the second electrode, wherein the light-emitting layer includes the compound represented by Formula 1.
상술한 화학식 1로 표시되는 화합물은 유기 발광 소자의 유기물층의 재료로서 사용될 수 있으며, 또한 용액 공정에 사용이 가능하며, 유기 발광 소자에서 효율의 향상, 낮은 구동전압 및/또는 수명 특성을 향상시킬 수 있다. The compound represented by the above-mentioned formula 1 can be used as a material for the organic layer of an organic light-emitting device, and can also be used in a solution process, and can improve efficiency, low driving voltage, and/or lifespan characteristics in organic light-emitting devices. there is.
도 1은 기판(1), 양극(2), 발광층(3), 음극(4)으로 이루어진 유기 발광 소자의 예를 도시한 것이다.
도 2는 기판 (1), 양극(2), 정공주입층(5), 정공수송층(6), 발광층(7), 전자주입 및 수송층(8) 및 음극(4)로 이루어진 유기 발광 소자의 예를 도시한 것이다.
도 3은 제조예 1에서 제조한 화합물 1의 GC-MS 데이터를 나타낸 것이다.
도 4는 제조예 2에서 제조한 화합물 2의 GC-MS 데이터를 나타낸 것이다.Figure 1 shows an example of an organic light emitting device consisting of a substrate 1, an anode 2, a light emitting layer 3, and a cathode 4.
Figure 2 is an example of an organic light emitting device consisting of a substrate (1), an anode (2), a hole injection layer (5), a hole transport layer (6), a light emitting layer (7), an electron injection and transport layer (8), and a cathode (4). It shows.
Figure 3 shows GC-MS data of Compound 1 prepared in Preparation Example 1.
Figure 4 shows GC-MS data of Compound 2 prepared in Preparation Example 2.
이하, 본 발명의 이해를 돕기 위하여 보다 상세히 설명한다.Hereinafter, the present invention will be described in more detail to aid understanding.
(용어의 정의)(Definition of Terms)
본 명세서에서, 는 다른 치환기에 연결되는 결합을 의미한다.In this specification, means a bond connected to another substituent.
본 명세서에서 "치환 또는 비치환된" 이라는 용어는 중수소; 할로겐기; 시아노기; 니트로기; 히드록시기; 카보닐기; 에스테르기; 이미드기; 아미노기; 포스핀옥사이드기; 알콕시기; 아릴옥시기; 알킬티옥시기; 아릴티옥시기; 알킬술폭시기; 아릴술폭시기; 실릴기; 붕소기; 알킬기; 사이클로알킬기; 알케닐기; 아릴기; 아르알킬기; 아르알케닐기; 알킬아릴기; 알킬아민기; 아랄킬아민기; 헤테로아릴아민기; 아릴아민기; 아릴포스핀기; 또는 N, O 및 S 원자 중 1개 이상을 포함하는 헤테로아릴로 이루어진 군에서 선택된 1개 이상의 치환기로 치환 또는 비치환되거나, 상기 예시된 치환기 중 2 이상의 치환기가 연결된 치환 또는 비치환된 것을 의미한다. 예컨대, "2 이상의 치환기가 연결된 치환기"는 비페닐기일 수 있다. 즉, 비페닐이기는 아릴기일 수도 있고, 2개의 페닐기가 연결된 치환기로 해석될 수도 있다.As used herein, the term “substituted or unsubstituted” refers to deuterium; halogen group; Cyano group; nitro group; hydroxyl group; carbonyl group; ester group; imide group; amino group; Phosphine oxide group; Alkoxy group; Aryloxy group; Alkylthioxy group; Arylthioxy group; Alkyl sulphoxy group; Aryl sulfoxy group; silyl group; boron group; Alkyl group; Cycloalkyl group; alkenyl group; Aryl group; Aralkyl group; Aralkenyl group; Alkylaryl group; Alkylamine group; Aralkylamine group; heteroarylamine group; Arylamine group; Arylphosphine group; or substituted or unsubstituted with one or more substituents selected from the group consisting of heteroaryl containing one or more of N, O and S atoms, or substituted or unsubstituted with two or more of the above-exemplified substituents linked. . For example, “a substituent group in which two or more substituents are connected” may be a biphenyl group. That is, the biphenyl group may be an aryl group, or it may be interpreted as a substituent in which two phenyl groups are connected.
본 명세서에서 카보닐기의 탄소수는 특별히 한정되지 않으나, 탄소수 1 내지 40인 것이 바람직하다. 구체적으로 하기와 같은 구조의 화합물이 될 수 있으나, 이에 한정되는 것은 아니다.In this specification, the carbon number of the carbonyl group is not particularly limited, but is preferably 1 to 40 carbon atoms. Specifically, it may be a compound with the following structure, but is not limited thereto.
본 명세서에 있어서, 에스테르기는 에스테르기의 산소가 탄소수 1 내지 25의 직쇄, 분지쇄 또는 고리쇄 알킬기 또는 탄소수 6 내지 25의 아릴기로 치환될 수 있다. 구체적으로, 하기 구조식의 화합물이 될 수 있으나, 이에 한정되는 것은 아니다.In the present specification, the oxygen of the ester group may be substituted with a straight-chain, branched-chain, or ring-chain alkyl group having 1 to 25 carbon atoms or an aryl group having 6 to 25 carbon atoms. Specifically, it may be a compound of the following structural formula, but is not limited thereto.
본 명세서에 있어서, 이미드기의 탄소수는 특별히 한정되지 않으나, 탄소수 1 내지 25인 것이 바람직하다. 구체적으로 하기와 같은 구조의 화합물이 될 수 있으나, 이에 한정되는 것은 아니다.In this specification, the carbon number of the imide group is not particularly limited, but is preferably 1 to 25 carbon atoms. Specifically, it may be a compound with the following structure, but is not limited thereto.
본 명세서에 있어서, 실릴기는 구체적으로 트리메틸실릴기, 트리에틸실릴기, t-부틸디메틸실릴기, 비닐디메틸실릴기, 프로필디메틸실릴기, 트리페닐실릴기, 디페닐실릴기, 페닐실릴기 등이 있으나 이에 한정되지 않는다. In the present specification, the silyl group specifically includes trimethylsilyl group, triethylsilyl group, t-butyldimethylsilyl group, vinyldimethylsilyl group, propyldimethylsilyl group, triphenylsilyl group, diphenylsilyl group, phenylsilyl group, etc. However, it is not limited to this.
본 명세서에 있어서, 붕소기는 구체적으로 트리메틸붕소기, 트리에틸붕소기, t-부틸디메틸붕소기, 트리페닐붕소기, 페닐붕소기 등이 있으나 이에 한정되지 않는다.In this specification, the boron group specifically includes trimethyl boron group, triethyl boron group, t-butyldimethyl boron group, triphenyl boron group, and phenyl boron group, but is not limited thereto.
본 명세서에 있어서, 할로겐기의 예로는 불소, 염소, 브롬 또는 요오드가 있다.In this specification, examples of halogen groups include fluorine, chlorine, bromine, or iodine.
본 명세서에 있어서, 상기 알킬기는 직쇄(선형) 또는 분지쇄(분지형)일 수 있고, 탄소수는 특별히 한정되지 않으나 1 내지 40인 것이 바람직하다. 일 실시상태에 따르면, 상기 알킬기의 탄소수는 1 내지 20이다. 또 하나의 실시상태에 따르면, 상기 알킬기의 탄소수는 1 내지 10이다. 또 하나의 실시상태에 따르면, 상기 알킬기의 탄소수는 1 내지 6이다. 알킬기의 구체적인 예로는 메틸, 에틸, 프로필, n-프로필, 이소프로필, 부틸, n-부틸, 이소부틸, tert-부틸, sec-부틸, 1-메틸-부틸, 1-에틸-부틸, 펜틸, n-펜틸, 이소펜틸, 네오펜틸, tert-펜틸, 헥실, n-헥실, 1-메틸펜틸, 2-메틸펜틸, 4-메틸-2-펜틸, 3,3-디메틸부틸, 2-에틸부틸, 헵틸, n-헵틸, 1-메틸헥실, 사이클로펜틸메틸, 사이클로헥틸메틸, 옥틸, n-옥틸, tert-옥틸, 1-메틸헵틸, 2-에틸헥실, 2-프로필펜틸, n-노닐, 2,2-디메틸헵틸, 1-에틸-프로필, 1,1-디메틸-프로필, 이소헥실, 2-메틸펜틸, 4-메틸헥실, 5-메틸헥실 등이 있으나, 이들에 한정되지 않는다.In the present specification, the alkyl group may be straight chain (linear) or branched (branched), and the number of carbon atoms is not particularly limited, but is preferably 1 to 40. According to one embodiment, the carbon number of the alkyl group is 1 to 20. According to another embodiment, the carbon number of the alkyl group is 1 to 10. According to another embodiment, the carbon number of the alkyl group is 1 to 6. Specific examples of alkyl groups include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n. -pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl , n-heptyl, 1-methylhexyl, cyclopentylmethyl, cyclohexylmethyl, octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhexyl, 2-propylpentyl, n-nonyl, 2,2 -Dimethylheptyl, 1-ethyl-propyl, 1,1-dimethyl-propyl, isohexyl, 2-methylpentyl, 4-methylhexyl, 5-methylhexyl, etc., but is not limited to these.
본 명세서에 있어서, 상기 알케닐기는 직쇄 또는 분지쇄일 수 있고, 탄소수는 특별히 한정되지 않으나, 2 내지 40인 것이 바람직하다. 일 실시상태에 따르면, 상기 알케닐기의 탄소수는 2 내지 20이다. 또 하나의 실시상태에 따르면, 상기 알케닐기의 탄소수는 2 내지 10이다. 또 하나의 실시상태에 따르면, 상기 알케닐기의 탄소수는 2 내지 6이다. 구체적인 예로는 비닐, 1-프로페닐, 이소프로페닐, 1-부테닐, 2-부테닐, 3-부테닐, 1-펜테닐, 2-펜테닐, 3-펜테닐, 3-메틸-1-부테닐, 1,3-부타디에닐, 알릴, 1-페닐비닐-1-일, 2-페닐비닐-1-일, 2,2-디페닐비닐-1-일, 2-페닐-2-(나프틸-1-일)비닐-1-일, 2,2-비스(디페닐-1-일)비닐-1-일, 스틸베닐기, 스티레닐기 등이 있으나 이들에 한정되지 않는다.In the present specification, the alkenyl group may be straight chain or branched, and the number of carbon atoms is not particularly limited, but is preferably 2 to 40. According to one embodiment, the alkenyl group has 2 to 20 carbon atoms. According to another embodiment, the alkenyl group has 2 to 10 carbon atoms. According to another embodiment, the alkenyl group has 2 to 6 carbon atoms. Specific examples include vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 3-methyl-1- Butenyl, 1,3-butadienyl, allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, 2,2-diphenylvinyl-1-yl, 2-phenyl-2-( Naphthyl-1-yl) vinyl-1-yl, 2,2-bis (diphenyl-1-yl) vinyl-1-yl, stilbenyl group, styrenyl group, etc., but are not limited to these.
본 명세서에 있어서, 사이클로알킬기는 특별히 한정되지 않으나, 탄소수 3 내지 60인 것이 바람직하며, 일 실시상태에 따르면, 상기 사이클로알킬기의 탄소수는 3 내지 30이다. 또 하나의 실시상태에 따르면, 상기 사이클로알킬기의 탄소수는 3 내지 20이다. 또 하나의 실시상태에 따르면, 상기 사이클로알킬기의 탄소수는 3 내지 6이다. 구체적으로 사이클로프로필, 사이클로부틸, 사이클로펜틸, 3-메틸사이클로펜틸, 2,3-디메틸사이클로펜틸, 사이클로헥실, 3-메틸사이클로헥실, 4-메틸사이클로헥실, 2,3-디메틸사이클로헥실, 3,4,5-트리메틸사이클로헥실, 4-tert-부틸사이클로헥실, 사이클로헵틸, 사이클로옥틸 등이 있으나, 이에 한정되지 않는다.In the present specification, the cycloalkyl group is not particularly limited, but preferably has 3 to 60 carbon atoms, and according to one embodiment, the cycloalkyl group has 3 to 30 carbon atoms. According to another embodiment, the carbon number of the cycloalkyl group is 3 to 20. According to another embodiment, the carbon number of the cycloalkyl group is 3 to 6. Specifically, cyclopropyl, cyclobutyl, cyclopentyl, 3-methylcyclopentyl, 2,3-dimethylcyclopentyl, cyclohexyl, 3-methylcyclohexyl, 4-methylcyclohexyl, 2,3-dimethylcyclohexyl, 3, Examples include, but are not limited to, 4,5-trimethylcyclohexyl, 4-tert-butylcyclohexyl, cycloheptyl, and cyclooctyl.
본 명세서에 있어서, 아릴기는 특별히 한정되지 않으나 탄소수 6 내지 60인 것이 바람직하며, 단환식 아릴기 또는 다환식 아릴기일 수 있다. 일 실시상태에 따르면, 상기 아릴기의 탄소수는 6 내지 30이다. 일 실시상태에 따르면, 상기 아릴기의 탄소수는 6 내지 20이다. 상기 아릴기가 단환식 아릴기로는 페닐기, 비페닐이기, 터페닐기 등이 될 수 있으나, 이에 한정되는 것은 아니다. 상기 다환식 아릴기로는 나프틸기, 안트라세닐기, 페난쓰레닐기, 파이레닐기, 페릴레닐기, 크라이세닐기, 플루오레닐기 등이 될 수 있으나, 이에 한정되는 것은 아니다.In the present specification, the aryl group is not particularly limited, but preferably has 6 to 60 carbon atoms, and may be a monocyclic aryl group or a polycyclic aryl group. According to one embodiment, the aryl group has 6 to 30 carbon atoms. According to one embodiment, the aryl group has 6 to 20 carbon atoms. The aryl group may be a monocyclic aryl group, such as a phenyl group, a biphenyl group, or a terphenyl group, but is not limited thereto. The polycyclic aryl group may be a naphthyl group, anthracenyl group, phenanthrenyl group, pyrenyl group, perylenyl group, chrysenyl group, fluorenyl group, etc., but is not limited thereto.
본 명세서에 있어서, 플루오레닐기는 치환될 수 있고, 치환기 2개가 서로 결합하여 스피로 구조를 형성할 수 있다. 상기 플루오레닐기가 치환되는 경우, 등이 될 수 있다. 다만, 이에 한정되는 것은 아니다.In the present specification, the fluorenyl group may be substituted, and two substituents may be combined with each other to form a spiro structure. When the fluorenyl group is substituted, It can be etc. However, it is not limited to this.
본 명세서에 있어서, 헤테로아릴은 이종 원소로 O, N, Si 및 S 중 1개 이상을 포함하는 헤테로아릴로서, 탄소수는 특별히 한정되지 않으나, 탄소수 2 내지 60인 것이 바람직하다. 헤테로아릴의 예로는 티오펜기, 퓨란기, 피롤기, 이미다졸기, 티아졸기, 옥사졸기, 옥사디아졸기, 트리아졸기, 피리딜기, 비피리딜기, 피리미딜기, 트리아진기, 아크리딜기, 피리다진기, 피라지닐기, 퀴놀리닐기, 퀴나졸린기, 퀴녹살리닐기, 프탈라지닐기, 피리도 피리미디닐기, 피리도 피라지닐기, 피라지노 피라지닐기, 이소퀴놀린기, 인돌기, 카바졸기, 벤즈옥사졸기, 벤조이미다졸기, 벤조티아졸기, 벤조카바졸기, 벤조티오펜기, 디벤조티오펜기, 벤조퓨라닐기, 페난쓰롤린기(phenanthroline), 이소옥사졸릴기, 티아디아졸릴기, 페노티아지닐기 및 디벤조퓨라닐기 등이 있으나, 이들에만 한정되는 것은 아니다.In the present specification, heteroaryl is a heteroaryl containing one or more of O, N, Si, and S as a heteroelement, and the number of carbon atoms is not particularly limited, but is preferably 2 to 60 carbon atoms. Examples of heteroaryl include thiophene group, furan group, pyrrole group, imidazole group, thiazole group, oxazole group, oxadiazole group, triazole group, pyridyl group, bipyridyl group, pyrimidyl group, triazine group, acridyl group, Pyridazine group, pyrazinyl group, quinolinyl group, quinazoline group, quinoxalinyl group, phthalazinyl group, pyrido pyrimidinyl group, pyrido pyrazinyl group, pyrazino pyrazinyl group, isoquinoline group, indole group, Carbazole group, benzoxazole group, benzoimidazole group, benzothiazole group, benzocarbazole group, benzothiophene group, dibenzothiophene group, benzofuranyl group, phenanthroline group, isoxazolyl group, thiadiazolyl group group, phenothiazinyl group, and dibenzofuranyl group, but are not limited to these.
본 명세서에 있어서, 아르알킬기, 아르알케닐기, 알킬아릴기, 아릴아민기, 아릴실릴기 중의 아릴기는 전술한 아릴기의 예시와 같다. 본 명세서에 있어서, 아르알킬기, 알킬아릴기, 알킬아민기 중 알킬기는 전술한 알킬기의 예시와 같다. 본 명세서에 있어서, 헤테로아릴아민 중 헤테로아릴은 전술한 헤테로아릴에 관한 설명이 적용될 수 있다. 본 명세서에 있어서, 아르알케닐기 중 알케닐기는 전술한 알케닐기의 예시와 같다. 본 명세서에 있어서, 아릴렌은 2가기인 것을 제외하고는 전술한 아릴기에 관한 설명이 적용될 수 있다. 본 명세서에 있어서, 헤테로아릴렌은 2가기인 것을 제외하고는 전술한 헤테로아릴에 관한 설명이 적용될 수 있다. 본 명세서에 있어서, 탄화수소 고리는 1가기가 아니고, 2개의 치환기가 결합하여 형성한 것을 제외하고는 전술한 아릴기 또는 사이클로알킬기에 관한 설명이 적용될 수 있다. 본 명세서에 있어서, 헤테로고리는 1가기가 아니고, 2개의 치환기가 결합하여 형성한 것을 제외하고는 전술한 헤테로아릴에 관한 설명이 적용될 수 있다.In this specification, the aryl group among the aralkyl group, aralkenyl group, alkylaryl group, arylamine group, and arylsilyl group is the same as the example of the aryl group described above. In this specification, the aralkyl group, alkylaryl group, and alkylamine group are the same as the examples of the alkyl group described above. In the present specification, the description regarding heteroaryl described above may be applied to heteroaryl among heteroarylamines. In this specification, the alkenyl group among the aralkenyl groups is the same as the example of the alkenyl group described above. In the present specification, the description of the aryl group described above can be applied, except that arylene is a divalent group. In the present specification, the description of heteroaryl described above can be applied, except that heteroarylene is a divalent group. In the present specification, the description of the aryl group or cycloalkyl group described above can be applied, except that the hydrocarbon ring is not monovalent and is formed by combining two substituents. In the present specification, the description of heteroaryl described above can be applied, except that the heterocycle is not monovalent and is formed by combining two substituents.
(화합물)(compound)
한편, 본 발명은 상기 화학식 1로 표시되는 안트라센 유도체 화합물을 제공한다. Meanwhile, the present invention provides an anthracene derivative compound represented by Formula 1 above.
종래에 진공 증착 공정에 사용되던 물질은, 용매에 대한 용해도가 매우 낮거나, 특정 용매에 대해서만 용해도가 높아 용액 공정에 사용되기 어렵다는 문제가 있었다.Previously, materials used in vacuum deposition processes had a problem in that they had very low solubility in solvents or had high solubility only in specific solvents, making them difficult to use in solution processes.
그러나 본 발명에 따른 화합물은, 이하 상세히 설명할 바와 같이 상기 화학식 1로 표시되는 구조를 가져, 용액 공정에 사용되는 여러 용매에 대한 용해도가 높아 유기 발광 소자 제조 시 용액 공정에 사용 가능하다.However, as will be described in detail below, the compound according to the present invention has the structure represented by Chemical Formula 1, and has high solubility in various solvents used in the solution process, so it can be used in the solution process when manufacturing organic light-emitting devices.
바람직하게는, L1 및 L2는 각각 독립적으로, 단일결합, 또는 페닐렌이다. 보다 바람직하게는, L1 및 L2는 각각 독립적으로, 단일결합, 1,3-페닐렌, 또는 1,4-페닐렌이다.Preferably, L 1 and L 2 are each independently a single bond or phenylene. More preferably, L 1 and L 2 are each independently a single bond, 1,3-phenylene, or 1,4-phenylene.
바람직하게는, Ar1 및 Ar2는 각각 독립적으로, 비치환되거나, 또는 1개 또는 2개의 C1-10 알킬로 치환된 C6-20 아릴이다. 이때, Ar1 및 Ar2는 서로 동일하거나, 또는 서로 상이할 수 있다.Preferably, Ar 1 and Ar 2 are each independently C 6-20 aryl that is unsubstituted or substituted with 1 or 2 C 1-10 alkyl. At this time, Ar 1 and Ar 2 may be the same or different from each other.
보다 바람직하게는, Ar1은 C6-20 아릴이고, Ar2는 비치환되거나, 또는 1개 또는 2개의 C1-4 알킬로 치환된 C6-20 아릴이다. More preferably, Ar 1 is C 6-20 aryl and Ar 2 is unsubstituted or C 6-20 aryl substituted with one or two C 1-4 alkyls.
보다 바람직하게는, Ar1은 페닐 또는 나프틸이고, Ar2는 비치환되거나, 또는 메틸, 에틸, 프로필, 이소프로필, 부틸 및 tert-부틸로 구성되는 군으로부터 각각 독립적으로 선택되는 1개 또는 2개의 치환기로 치환된 페닐; 또는 비치환되거나, 또는 메틸, 에틸, 프로필, 이소프로필, 부틸 및 tert-부틸로 구성되는 군으로부터 각각 독립적으로 선택되는 1개 또는 2개의 치환기로 치환된 나프틸이다. More preferably, Ar 1 is phenyl or naphthyl, and Ar 2 is unsubstituted or 1 or 2 each independently selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl and tert-butyl. phenyl substituted with two substituents; or naphthyl, which is unsubstituted or substituted with one or two substituents each independently selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, and tert-butyl.
가장 바람직하게는, Ar1 및 Ar2는 각각 독립적으로, 하기로 구성되는 군으로부터 선택되는 어느 하나이다:Most preferably, Ar 1 and Ar 2 are each independently selected from the group consisting of:
바람직하게는, L1 및 L2가 서로 동일하고, Ar1 및 Ar2가 서로 동일하거나;Preferably, L 1 and L 2 are the same as each other, and Ar 1 and Ar 2 are the same as each other;
L1 및 L2는 서로 상이하고, Ar1 및 Ar2가 서로 동일하거나; 또는 L 1 and L 2 are different from each other and Ar 1 and Ar 2 are the same as each other; or
L1 및 L2가 서로 상이하고, Ar1 및 Ar2가 서로 상이하다.L 1 and L 2 are different from each other, and Ar 1 and Ar 2 are different from each other.
예를 들어, 상기 화합물은 하기 화합물로 구성되는 군으로부터 선택되는 어느 하나이다: For example, the compound is any one selected from the group consisting of the following compounds:
한편, 상기 화학식 1로 표시되는 화합물은 일례로 하기 반응식 1과 같은 제조 방법으로 제조할 수 있다:Meanwhile, the compound represented by Formula 1 can be prepared, for example, by a production method as shown in Scheme 1 below:
[반응식 1][Scheme 1]
상기 반응식 1에서, X는 할로겐이고, L1, L2, Ar1 및 Ar2에 대한 설명은 상기 화학식 1에서 정의한 바와 같다. 상기 단계 1-1은 나프탈렌의 1번 위치에 보로란기를 도입하는 단계이고, 상기 단계 1-2는 스즈키 커플링 반응을 통해 안트라세닐기를 도입하는 단계이며, 상기 단계 1-3 및 1-4는 스즈키 커플링 반응을 한 번 더 진행하기 위해 나프탈렌의 7번 위치에 보로란기를 도입하는 단계이고, 상기 단계 1-5는 스즈키 커플링 반응을 통해 상기 화학식 1로 표시되는 화합물을 제조하는 단계이다. In Scheme 1 , Step 1-1 is a step of introducing a borolane group at position 1 of naphthalene, step 1-2 is a step of introducing an anthracenyl group through a Suzuki coupling reaction, and steps 1-3 and 1-4 are In order to proceed with the Suzuki coupling reaction once more, a borolane group is introduced into the 7th position of naphthalene, and steps 1-5 are steps for preparing the compound represented by Formula 1 through the Suzuki coupling reaction.
또는, 상기 화학식 1로 표시되는 화합물은 L1 및 L2가 서로 동일하고, Ar1 및 Ar2가 서로 동일한 경우에는 하기 반응식 2와 같은 제조 방법으로 제조할 수 있다:Alternatively, when L 1 and L 2 are the same as each other and Ar 1 and Ar 2 are the same as each other, the compound represented by Formula 1 can be prepared by the preparation method shown in Scheme 2 below:
[반응식 2][Scheme 2]
상기 반응식 2에서, X는 할로겐이고, L1, L2, Ar1 및 Ar2에 대한 설명은 상기 화학식 1에서 정의한 바와 같다. 상기 제조 방법은 후술할 제조예에서 보다 구체화될 수 있다. 상기 단계 2-1 및 2-2는 스즈키 커플링 반응을 위한 보로란기를 도입하는 단계이고, 상기 단계 2-3은 나프탈렌 1번 및 7번 위치에 스즈키 커플링 반응을 동시에 진행하여 상기 화학식 1로 표시되는 화합물을 제조하는 단계이다. In Scheme 2 , The manufacturing method may be further detailed in the manufacturing examples described later. Steps 2-1 and 2-2 are steps for introducing a borolan group for a Suzuki coupling reaction, and step 2-3 is a step of simultaneously performing a Suzuki coupling reaction at positions 1 and 7 of naphthalene to obtain Formula 1 This is the step of manufacturing the displayed compound.
이때, 상기 반응식 1 및 2의 스즈키 커플링 반응은 팔라듐 촉매와 염기의 존재 하에 수행하는 방법이 바람직하며, 상기 제조 방법은 후술하는 제조예에서 보다 구체화 될 수 있다.At this time, the Suzuki coupling reaction of Schemes 1 and 2 is preferably performed in the presence of a palladium catalyst and a base, and the preparation method can be further specified in the preparation examples described later.
(코팅 조성물) (Coating composition)
한편, 본 발명에 따른 화합물은 용액 공정으로 유기 발광 소자의 유기물 층, 특히 발광층을 형성할 수 있다. 구체적으로, 상기 화합물은 발광층의 호스트 재료로 사용될 수 있다. 이를 위하여, 본 발명은 상술한 본 발명에 따른 화합물 및 용매를 포함하는 코팅 조성물을 제공한다. Meanwhile, the compound according to the present invention can form an organic layer, especially a light-emitting layer, of an organic light-emitting device through a solution process. Specifically, the compound can be used as a host material for the light-emitting layer. For this purpose, the present invention provides a coating composition comprising the compound and solvent according to the present invention described above.
상기 용매는 본 발명에 따른 화합물을 용해 또는 분산시킬 수 있는 용매이면 특별히 제한되지 않으며, 일례로 클로로포름, 염화메틸렌, 1,2-디클로로에탄, 1,1,2-트리클로로에탄, 클로로벤젠, o-디클로로벤젠 등의 염소계 용매; 테트라하이드로퓨란, 디옥산 등의 에테르계 용매; 톨루엔, 크실렌, 트리메틸벤젠, 메시틸렌 등의 방향족 탄화수소계 용매; 시클로헥산, 메틸시클로헥산, n-펜탄, n-헥산, n-헵탄, n-옥탄, n-노난, n-데칸 등의 지방족 탄화수소계 용매; 아세톤, 메틸에틸케톤, 시클로헥사논 등의 케톤계 용매; 아세트산에틸, 아세트산부틸, 에틸셀로솔브아세테이트 등의 에스테르계 용매; 에틸렌글리콜, 에틸렌글리콜모노부틸에테르, 에틸렌글리콜모노에틸에테르, 에틸렌글리콜모노메틸에테르, 디메톡시에탄, 프로필렌글리콜, 디에톡시메탄, 트리에틸렌글리콜모노에틸에테르, 글리세린, 1,2-헥산디올 등의 다가 알코올 및 그의 유도체; 메탄올, 에탄올, 프로판올, 이소프로판올, 시클로헥산올 등의 알코올계 용매; 디메틸술폭사이드 등의 술폭사이드계 용매; 및 N-메틸-2-피롤리돈, N,N-디메틸포름아미드 등의 아미드계 용매; 부틸벤조에이트, 메틸-2-메톡시벤조에이트 등의 벤조에이트계 용매; 테트랄린; 3-페녹시톨루엔 등의 용매를 들 수 있다. 또한, 상술한 용매를 1종 단독으로 사용하거나 2종 이상의 용매를 혼합하여 사용할 수 있다. The solvent is not particularly limited as long as it is capable of dissolving or dispersing the compound according to the present invention, and examples include chloroform, methylene chloride, 1,2-dichloroethane, 1,1,2-trichloroethane, chlorobenzene, o -Chlorine-based solvents such as dichlorobenzene; Ether-based solvents such as tetrahydrofuran and dioxane; Aromatic hydrocarbon solvents such as toluene, xylene, trimethylbenzene, and mesitylene; Aliphatic hydrocarbon solvents such as cyclohexane, methylcyclohexane, n-pentane, n-hexane, n-heptane, n-octane, n-nonane, and n-decane; Ketone-based solvents such as acetone, methyl ethyl ketone, and cyclohexanone; Ester solvents such as ethyl acetate, butyl acetate, and ethyl cellosolve acetate; Polyhydric acids such as ethylene glycol, ethylene glycol monobutyl ether, ethylene glycol monoethyl ether, ethylene glycol monomethyl ether, dimethoxyethane, propylene glycol, diethoxymethane, triethylene glycol monoethyl ether, glycerin, 1,2-hexanediol, etc. alcohol and its derivatives; Alcohol-based solvents such as methanol, ethanol, propanol, isopropanol, and cyclohexanol; Sulfoxide-based solvents such as dimethyl sulfoxide; and amide-based solvents such as N-methyl-2-pyrrolidone and N,N-dimethylformamide; Benzoate-based solvents such as butyl benzoate and methyl-2-methoxybenzoate; tetralin; Solvents such as 3-phenoxytoluene can be mentioned. In addition, the above-mentioned solvents may be used individually or two or more types of solvents may be mixed.
또한, 상기 코팅 조성물은 도펀트 재료로 사용되는 화합물을 더 포함할 수 있고, 상기 도펀트 재료에 사용되는 화합물에 대한 설명은 후술한다.In addition, the coating composition may further include a compound used as a dopant material, and a description of the compound used as the dopant material will be provided later.
또한, 상기 코팅 조성물 내 본 발명에 따른 화합물의 농도는 0.1 wt/v% 내지 20 wt/v%인 것이 바람직하다. In addition, the concentration of the compound according to the present invention in the coating composition is preferably 0.1 wt/v% to 20 wt/v%.
바람직하게는, 상기 코팅 조성물의 용매에 대한 용해도(wt%, 25℃)는 용매 사이클로헥사논을 기준으로 1.5 wt% 초과 5.0 wt% 이하, 또는 1.5 wt% 초과 2.5wt% 이하이다. 이에 따라 상기 화학식 1로 표시되는 화합물을 포함하는 코팅 조성물은 용액 공정에 사용되기 적합하다.Preferably, the solubility (wt%, 25°C) of the coating composition in the solvent is greater than 1.5 wt% and 5.0 wt% or less, or greater than 1.5 wt% and 2.5 wt% or less based on the solvent cyclohexanone. Accordingly, the coating composition containing the compound represented by Formula 1 is suitable for use in a solution process.
또한, 본 발명은 상술한 코팅 조성물을 사용하여 발광층을 형성하는 방법을 제공한다. 구체적으로, 양극 상에, 또는 양극 상에 형성된 정공 수송층 상에 상술한 본 발명에 따른 발광층을 용액 공정으로 코팅하는 단계; 및 상기 코팅된 코팅 조성물을 열처리하는 단계를 포함한다. Additionally, the present invention provides a method of forming a light-emitting layer using the above-described coating composition. Specifically, coating the above-described light-emitting layer according to the present invention on the anode or on the hole transport layer formed on the anode by a solution process; and heat treating the coated coating composition.
상기 용액 공정은 상술한 본 발명에 따른 코팅 조성물을 사용하는 것으로, 스핀 코팅, 딥코팅, 닥터 블레이딩, 잉크젯 프린팅, 스크린 프린팅, 스프레이법, 롤 코팅 등을 의미하지만, 이들만으로 한정되는 것은 아니다.The solution process uses the coating composition according to the present invention described above, and includes spin coating, dip coating, doctor blading, inkjet printing, screen printing, spraying, roll coating, etc., but is not limited to these.
상기 열처리 단계에서 열처리 온도는 150 내지 230℃가 바람직하다. 또한, 상기 열처리 시간은 1분 내지 3시간이고, 보다 바람직하게는 10분 내지 1시간이다. 또한, 상기 열처리는 아르곤, 질소 등의 불활성 기체 분위기에서 수행하는 것이 바람직하다. In the heat treatment step, the heat treatment temperature is preferably 150 to 230°C. Additionally, the heat treatment time is 1 minute to 3 hours, and more preferably 10 minutes to 1 hour. Additionally, the heat treatment is preferably performed in an inert gas atmosphere such as argon or nitrogen.
(유기 발광 소자)(Organic light emitting device)
또한, 본 발명은 상기 화학식 1로 표시되는 화합물을 포함하는 유기 발광 소자를 제공한다. 일례로, 본 발명은 제1 전극; 상기 제1 전극과 대향하여 구비된 제2 전극; 및 상기 제1 전극과 상기 제2 전극 사이에 구비된 발광층을 포함하는 유기 발광 소자로서, 상기 발광층은 상기 화학식 1로 표시되는 화합물을 포함하는, 유기 발광 소자를 제공한다.Additionally, the present invention provides an organic light-emitting device containing the compound represented by Formula 1 above. In one example, the present invention includes a first electrode; a second electrode provided opposite to the first electrode; and an organic light-emitting device comprising a light-emitting layer provided between the first electrode and the second electrode, wherein the light-emitting layer includes the compound represented by Formula 1.
또한, 본 발명에 따른 유기 발광 소자는, 기판 상에 양극, 1층 이상의 유기물층 및 음극이 순차적으로 적층된 구조(normal type)의 유기 발광 소자일 수 있다. 또한, 본 발명에 따른 유기 발광 소자는 기판 상에 음극, 1층 이상의 유기물층 및 양극이 순차적으로 적층된 역방향 구조(inverted type)의 유기 발광 소자일 수 있다. 예컨대, 본 발명의 일실시예에 따른 유기 발광 소자의 구조는 도 1 및 2에 예시되어 있다.Additionally, the organic light emitting device according to the present invention may be a normal type organic light emitting device in which an anode, one or more organic material layers, and a cathode are sequentially stacked on a substrate. Additionally, the organic light emitting device according to the present invention may be an inverted type organic light emitting device in which a cathode, one or more organic material layers, and an anode are sequentially stacked on a substrate. For example, the structure of an organic light emitting device according to an embodiment of the present invention is illustrated in FIGS. 1 and 2.
도 1은 기판(1), 양극(2), 발광층(3), 음극(4)으로 이루어진 유기 발광 소자의 예를 도시한 것이다. 이와 같은 구조에 있어서, 상기 화학식 1로 표시되는 화합물은 상기 발광층에 포함될 수 있다. Figure 1 shows an example of an organic light emitting device consisting of a substrate 1, an anode 2, a light emitting layer 3, and a cathode 4. In this structure, the compound represented by Formula 1 may be included in the light-emitting layer.
도 2는 기판 (1), 양극(2), 정공주입층(5), 정공수송층(6), 발광층(7), 전자주입 및 수송층(8) 및 음극(4)로 이루어진 유기 발광 소자의 예를 도시한 것이다. 이와 같은 구조에 있어서, 상기 화학식 1로 표시되는 화합물은 상기 발광층에 포함될 수 있다.Figure 2 is an example of an organic light emitting device consisting of a substrate (1), an anode (2), a hole injection layer (5), a hole transport layer (6), a light emitting layer (7), an electron injection and transport layer (8), and a cathode (4). It shows. In this structure, the compound represented by Formula 1 may be included in the light-emitting layer.
본 발명에 따른 유기 발광 소자는, 상기 발광층이 본 발명에 따른 화합물을 포함하고, 상술한 방법과 같이 제조되는 것을 제외하고는 당 기술분야에 알려져 있는 재료와 방법으로 제조할 수 있다.The organic light emitting device according to the present invention can be manufactured using materials and methods known in the art, except that the light emitting layer contains the compound according to the present invention and is manufactured according to the method described above.
예컨대, 본 발명에 따른 유기 발광 소자는 기판 상에 양극, 유기물층 및 음극을 순차적으로 적층시켜 제조할 수 있다. 이때, 스퍼터링법(sputtering)이나 전자빔 증발법(e-beam evaporation)과 같은 PVD(physical Vapor Deposition) 방법을 이용하여, 기판 상에 금속 또는 전도성을 가지는 금속 산화물 또는 이들의 합금을 증착시켜 양극을 형성하고, 그 위에 정공 주입층, 정공 수송층, 발광층 및 전자 수송층을 포함하는 유기물 층을 형성한 후, 그 위에 음극으로 사용할 수 있는 물질을 증착시켜 제조할 수 있다. For example, the organic light emitting device according to the present invention can be manufactured by sequentially stacking an anode, an organic material layer, and a cathode on a substrate. At this time, an anode is formed by depositing a metal or a conductive metal oxide or an alloy thereof on the substrate using a physical vapor deposition (PVD) method such as sputtering or e-beam evaporation. It can be manufactured by forming an organic material layer including a hole injection layer, a hole transport layer, a light emitting layer, and an electron transport layer thereon, and then depositing a material that can be used as a cathode thereon.
이와 같은 방법 외에도, 기판 상에 음극 물질로부터 유기물층, 양극 물질을 차례로 증착시켜 유기 발광 소자를 제조할 수 있다(WO 2003/012890). 다만, 제조 방법이 이에 한정되는 것은 아니다. In addition to this method, an organic light-emitting device can be manufactured by sequentially depositing a cathode material, an organic layer, and an anode material on a substrate (WO 2003/012890). However, the manufacturing method is not limited to this.
이와 같은 방법 외에도, 기판 상에 음극 물질로부터 유기물층, 양극 물질을 차례로 증착시켜 유기 발광 소자를 제조할 수 있다(WO 2003/012890). 다만, 제조 방법이 이에 한정되는 것은 아니다. In addition to this method, an organic light-emitting device can be manufactured by sequentially depositing a cathode material, an organic layer, and an anode material on a substrate (WO 2003/012890). However, the manufacturing method is not limited to this.
일례로, 상기 제1 전극은 양극이고, 상기 제2 전극은 음극이거나, 또는 상기 제1 전극은 음극이고, 상기 제2 전극은 양극이다.In one example, the first electrode is an anode and the second electrode is a cathode, or the first electrode is a cathode and the second electrode is an anode.
상기 양극 물질로는 통상 유기물층으로 정공 주입이 원활할 수 있도록 일함수가 큰 물질이 바람직하다. 상기 양극 물질의 구체적인 예로는 바나듐, 크롬, 구리, 아연, 금과 같은 금속 또는 이들의 합금; 아연 산화물, 인듐 산화물, 인듐주석 산화물(ITO), 인듐아연 산화물(IZO)과 같은 금속 산화물; ZnO:Al 또는 SNO2:Sb와 같은 금속과 산화물의 조합; 폴리(3-메틸티오펜), 폴리[3,4-(에틸렌-1,2-디옥시)티오펜](PEDOT), 폴리피롤 및 폴리아닐린과 같은 전도성 화합물 등이 있으나, 이들에만 한정되는 것은 아니다. The anode material is generally preferably a material with a large work function to facilitate hole injection into the organic layer. Specific examples of the anode material include metals such as vanadium, chromium, copper, zinc, and gold, or alloys thereof; metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO); Combinations of metals and oxides such as ZnO:Al or SNO 2 :Sb; Conductive compounds such as poly(3-methylthiophene), poly[3,4-(ethylene-1,2-dioxy)thiophene](PEDOT), polypyrrole, and polyaniline are included, but are not limited to these.
상기 음극 물질로는 통상 유기물층으로 전자 주입이 용이하도록 일함수가 작은 물질인 것이 바람직하다. 상기 음극 물질의 구체적인 예로는 마그네슘, 칼슘, 나트륨, 칼륨, 티타늄, 인듐, 이트륨, 리튬, 가돌리늄, 알루미늄, 은, 주석 및 납과 같은 금속 또는 이들의 합금; LiF/Al 또는 LiO2/Al과 같은 다층 구조 물질 등이 있으나, 이들에만 한정되는 것은 아니다. The cathode material is generally preferably a material with a small work function to facilitate electron injection into the organic layer. Specific examples of the negative electrode material include metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin, and lead, or alloys thereof; There are, but are not limited to, multi-layered materials such as LiF/Al or LiO 2 /Al.
상기 정공주입층은 전극으로부터 정공을 주입하는 층으로, 정공 주입 물질로는 정공을 수송하는 능력을 가져 양극에서의 정공 주입효과, 발광층 또는 발광재료에 대하여 우수한 정공 주입 효과를 갖고, 발광층에서 생성된 여기자의 전자주입층 또는 전자주입재료에의 이동을 방지하며, 또한, 박막 형성 능력이 우수한 화합물이 바람직하다. 정공 주입 물질의 HOMO(highest occupied molecular orbital)가 양극 물질의 일함수와 주변 유기물 층의 HOMO 사이인 것이 바람직하다. 정공 주입 물질의 구체적인 예로는 금속 포피린(porphyrin), 올리고티오펜, 아릴아민 계열의 유기물, 헥사니트릴헥사아자트리페닐렌 계열의 유기물, 퀴나크리돈(quinacridone)계열의 유기물, 페릴렌(perylene) 계열의 유기물, 안트라퀴논 및 폴리아닐린과 폴리티오펜 계열의 전도성 화합물 등이 있으나, 이들에만 한정 되는 것은 아니다. The hole injection layer is a layer that injects holes from an electrode. The hole injection material has the ability to transport holes, has an excellent hole injection effect at the anode, a light-emitting layer or a light-emitting material, and has an excellent hole injection effect on the light-emitting layer or light-emitting material. A compound that prevents movement of excitons to the electron injection layer or electron injection material and has excellent thin film forming ability is preferred. It is preferable that the highest occupied molecular orbital (HOMO) of the hole injection material is between the work function of the anode material and the HOMO of the surrounding organic material layer. Specific examples of hole injection materials include metal porphyrin, oligothiophene, arylamine-based organic substances, hexanitrilehexaazatriphenylene-based organic substances, quinacridone-based organic substances, and perylene-based organic substances. These include organic substances, anthraquinone, polyaniline, and polythiophene series conductive compounds, but are not limited to these.
상기 정공수송층은 정공주입층으로부터 정공을 수취하여 발광층까지 정공을 수송하는 층으로, 정공 수송 물질로는 양극이나 정공 주입층으로부터 정공을 수송받아 발광층으로 옮겨줄 수 있는 물질로 정공에 대한 이동성이 큰 물질이 적합하다. 구체적인 예로는 아릴아민 계열의 유기물, 전도성 화합물, 및 공액 부분과 비공액 부분이 함께 있는 블록 공중합체 등이 있으나, 이들에만 한정되는 것은 아니다. The hole transport layer is a layer that receives holes from the hole injection layer and transports holes to the light-emitting layer. The hole transport material is a material that can receive holes from the anode or hole injection layer and transfer them to the light-emitting layer, and has high mobility for holes. The material is suitable. Specific examples include arylamine-based organic materials, conductive compounds, and block copolymers with both conjugated and non-conjugated portions, but are not limited to these.
상기 발광 물질로는 정공 수송층과 전자 수송층으로부터 정공과 전자를 각각 수송받아 결합시킴으로써 가시광선 영역의 빛을 낼 수 있는 물질로서, 형광이나 인광에 대한 양자 효율이 좋은 물질이 바람직하다. 구체적인 예로 8-히드록시-퀴놀린 알루미늄 착물(Alq3); 카르바졸 계열 화합물; 이량체화 스티릴(dimerized styryl) 화합물; BAlq; 10-히드록시벤조 퀴놀린-금속 화합물; 벤족사졸, 벤즈티아졸 및 벤즈이미다졸 계열의 화합물; 폴리(p-페닐렌비닐렌)(PPV) 계열의 화합물; 스피로(spiro) 화합물; 폴리플루오렌, 루브렌 등이 있으나, 이들에만 한정되는 것은 아니다. The light-emitting material is a material capable of emitting light in the visible range by receiving and combining holes and electrons from the hole transport layer and the electron transport layer, respectively, and is preferably a material with good quantum efficiency for fluorescence or phosphorescence. Specific examples include 8-hydroxy-quinoline aluminum complex (Alq 3 ); Carbazole-based compounds; dimerized styryl compounds; BAlq; 10-hydroxybenzoquinoline-metal compound; Compounds of the benzoxazole, benzthiazole and benzimidazole series; Poly(p-phenylenevinylene) (PPV) series compounds; Spiro compounds; Polyfluorene, rubrene, etc., but are not limited to these.
상기 발광층은 상술한 바와 같이 호스트 재료 및 도펀트 재료를 포함할 수 있다. 호스트 재료는 상술한 화학식 1로 표시되는 화합물이 사용될 수 있다. 또는, 호스트 재료로 상기 화학식 1로 표시되는 화합물 이외에 축합 방향족환 유도체 또는 헤테로환 함유 화합물 등을 더 사용할 수 있다. 구체적으로 축합 방향족환 유도체로는 안트라센 유도체, 피렌 유도체, 나프탈렌 유도체, 펜타센 유도체, 페난트렌 화합물, 플루오란텐 화합물 등이 있고, 헤테로환 함유 화합물로는 카바졸 유도체, 디벤조퓨란 유도체, 래더형 퓨란 화합물, 피리미딘 유도체 등이 있으나, 이에 한정되지 않는다. The light emitting layer may include a host material and a dopant material as described above. The host material may be a compound represented by the above-mentioned formula (1). Alternatively, in addition to the compound represented by Formula 1, a condensed aromatic ring derivative or a heterocyclic ring-containing compound may be used as a host material. Specifically, condensed aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, and fluoranthene compounds, and heterocyclic ring-containing compounds include carbazole derivatives, dibenzofuran derivatives, and ladder-type compounds. These include, but are not limited to, furan compounds and pyrimidine derivatives.
도펀트 재료로는 방향족 아민 유도체, 스트릴아민 화합물, 붕소 착체, 플루오란텐 화합물, 금속 착체 등이 있다. 구체적으로 방향족 아민 유도체로는 치환 또는 비치환된 아릴아미노기를 갖는 축합 방향족환 유도체로서, 아릴아미노기를 갖는 피렌, 안트라센, 크리센, 페리플란텐 등이 있으며, 스티릴아민 화합물로는 치환 또는 비치환된 아릴아민에 적어도 1개의 아릴비닐기가 치환되어 있는 화합물로, 아릴기, 실릴기, 알킬기, 사이클로알킬기 및 아릴아미노기로 이루어진 군에서 1 또는 2 이상 선택되는 치환기가 치환 또는 비치환된다. 구체적으로 스티릴아민, 스티릴디아민, 스티릴트리아민, 스티릴테트라아민 등이 있으나, 이에 한정되지 않는다. 또한, 금속 착체로는 이리듐 착체, 백금 착체 등이 있으나, 이에 한정되지 않는다.Dopant materials include aromatic amine derivatives, strylamine compounds, boron complexes, fluoranthene compounds, and metal complexes. Specifically, aromatic amine derivatives include condensed aromatic ring derivatives having a substituted or unsubstituted arylamino group, such as pyrene, anthracene, chrysene, and periplanthene, and styrylamine compounds include substituted or unsubstituted arylamino groups. It is a compound in which at least one arylvinyl group is substituted on the arylamine, and is substituted or unsubstituted with one or two or more substituents selected from the group consisting of aryl group, silyl group, alkyl group, cycloalkyl group, and arylamino group. Specifically, styrylamine, styryldiamine, styryltriamine, styryltetraamine, etc. are included, but are not limited thereto. Additionally, metal complexes include, but are not limited to, iridium complexes and platinum complexes.
상기 전자수송층은 전자주입층으로부터 전자를 수취하여 발광층까지 전자를 수송하는 층으로, 전자 수송 물질로는 음극으로부터 전자를 잘 주입 받아 발광층으로 옮겨줄 수 있는 물질로서, 전자에 대한 이동성이 큰 물질이 적합하다. 구체적인 예로는 8-히드록시퀴놀린의 Al 착물; Alq3를 포함한 착물; 유기 라디칼 화합물; 히드록시플라본-금속 착물 등이 있으나, 이들에만 한정되는 것은 아니다. 전자 수송층은 종래기술에 따라 사용된 바와 같이 임의의 원하는 캐소드 물질과 함께 사용할 수 있다. 특히, 적절한 캐소드 물질의 예는 낮은 일함수를 가지고 알루미늄층 또는 실버층이 뒤따르는 통상적인 물질이다. 구체적으로 세슘, 바륨, 칼슘, 이테르븀 및 사마륨이고, 각 경우 알루미늄 층 또는 실버층이 뒤따른다.The electron transport layer is a layer that receives electrons from the electron injection layer and transports electrons to the light-emitting layer. The electron transport material is a material that can easily receive electrons from the cathode and transfer them to the light-emitting layer, and is a material with high electron mobility. Suitable. Specific examples include Al complex of 8-hydroxyquinoline; Complex containing Alq 3 ; organic radical compounds; Hydroxyflavone-metal complexes, etc., but are not limited to these. The electron transport layer can be used with any desired cathode material as used according to the prior art. In particular, examples of suitable cathode materials are conventional materials with a low work function followed by an aluminum or silver layer. Specifically, cesium, barium, calcium, ytterbium and samarium, in each case followed by an aluminum layer or a silver layer.
상기 전자주입층은 전극으로부터 전자를 주입하는 층으로, 전자를 수송하는 능력을 갖고, 음극으로부터의 전자 주입 효과, 발광층 또는 발광 재료에 대하여 우수한 전자주입 효과를 가지며, 발광층에서 생성된 여기자의 정공주입층에의 이동을 방지하고, 또한, 박막형성능력이 우수한 화합물이 바람직하다. 구체적으로는 LiF, NaF, NaCl, CsF, Li2O, BaO, 플루오레논, 안트라퀴노다이메탄, 다이페노퀴논, 티오피란 다이옥사이드, 옥사졸, 옥사다이아졸, 트리아졸, 이미다졸, 페릴렌테트라카복실산, 프레오레닐리덴 메탄, 안트론 등과 그들의 유도체, 금속 착체 화합물 및 질소 함유 5원환 유도체 등이 있으나, 이에 한정되지 않는다. The electron injection layer is a layer that injects electrons from the electrode, has the ability to transport electrons, has an excellent electron injection effect from the cathode, a light emitting layer or a light emitting material, and hole injection of excitons generated in the light emitting layer. A compound that prevents movement to the layer and has excellent thin film forming ability is preferred. Specifically, LiF, NaF, NaCl, CsF, Li 2 O, BaO, fluorenone, anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid. , preorenylidene methane, anthrone, etc. and their derivatives, metal complex compounds, and nitrogen-containing 5-membered ring derivatives, etc., but are not limited thereto.
상기 금속 착체 화합물로서는 8-하이드록시퀴놀리나토 리튬, 비스(8-하이드록시퀴놀리나토)아연, 비스(8-하이드록시퀴놀리나토)구리, 비스(8-하이드록시퀴놀리나토)망간, 트리스(8-하이드록시퀴놀리나토)알루미늄, 트리스(2-메틸-8-하이드록시퀴놀리나토)알루미늄, 트리스(8-하이드록시퀴놀리나토)갈륨, 비스(10-하이드록시벤조[h]퀴놀리나토)베릴륨, 비스(10-하이드록시벤조[h]퀴놀리나토)아연, 비스(2-메틸-8-퀴놀리나토)클로로갈륨, 비스(2-메틸-8-퀴놀리나토)(o-크레졸라토)갈륨, 비스(2-메틸-8-퀴놀리나토)(1-나프톨라토)알루미늄, 비스(2-메틸-8-퀴놀리나토)(2-나프톨라토)갈륨 등이 있으나, 이에 한정되지 않는다.Examples of the metal complex compounds include 8-hydroxyquinolinato lithium, bis(8-hydroxyquinolinato)zinc, bis(8-hydroxyquinolinato)copper, bis(8-hydroxyquinolinato)manganese, Tris(8-hydroxyquinolinato)aluminum, Tris(2-methyl-8-hydroxyquinolinato)aluminum, Tris(8-hydroxyquinolinato)gallium, bis(10-hydroxybenzo[h] Quinolinato)beryllium, bis(10-hydroxybenzo[h]quinolinato)zinc, bis(2-methyl-8-quinolinato)chlorogallium, bis(2-methyl-8-quinolinato)( o-cresolato) gallium, bis(2-methyl-8-quinolinato)(1-naphtolato) aluminum, bis(2-methyl-8-quinolinato)(2-naphtolato) gallium, etc. It is not limited to this.
본 발명에 따른 유기 발광 소자는 사용되는 재료에 따라 전면 발광형, 후면 발광형 또는 양면 발광형일 수 있다.The organic light emitting device according to the present invention may be a front emitting type, a back emitting type, or a double-sided emitting type depending on the material used.
또한, 본 발명에 따른 화합물은 유기 발광 소자 외에도 유기 태양 전지 또는 유기 트랜지스터에 포함될 수 있다.Additionally, the compound according to the present invention may be included in an organic solar cell or an organic transistor in addition to an organic light-emitting device.
상기 화학식 1로 표시되는 화합물 및 이를 포함하는 유기 발광 소자의 제조는 이하 실시예에서 구체적으로 설명한다. 그러나 하기 실시예는 본 발명을 예시하기 위한 것이며, 본 발명의 범위가 이들에 의하여 한정되는 것은 아니다.The preparation of the compound represented by Formula 1 and an organic light-emitting device containing the same will be described in detail in the following Examples. However, the following examples are for illustrating the present invention, and the scope of the present invention is not limited thereto.
제조예Manufacturing example 1: 화합물 1의 제조 1: Preparation of Compound 1
단계 1-1: 중간체 화합물 A의 합성Step 1-1: Synthesis of Intermediate Compound A
8-브로모나프탈렌-2-올(25.0 g, 1.0 eq.), B2Pin2(34.2 g, 1.2 eq.), KOAc(31.5 g, 2.86 eq.)를 둥근 바닥 플라스크에 넣고 무수 다이옥세인에 용해하였다. 이후, 10 분 동안 질소 가스를 충전해주며 상온에서 교반하고, 오일 용기 온도를 상온에서 120℃로 올려주었다. 이후, 용매가 끓기 시작하면 Pd(dppf)Cl2·디클로로메탄(8.2 g, 9 mol%)을 적가 한 뒤, 하룻밤 동안 교반하였다. 반응 후, 디클로로메탄과 물로 수세하여 유기층을 분리하고, MgSO4로 물을 제거하고 산성백토, 팔라듐 차콜로 팔라듐을 흡착한 뒤 셀라이트 패드를 통과시켰다. 통과된 용액을 감압 하에 농축시킨 뒤, 컬럼 크로마토그래피를 통해 정제하여 중간체 화합물 A 23.3 g(수율 77%)을 얻었다. 8-Bromonaphthalen-2-ol (25.0 g, 1.0 eq.), B 2 Pin 2 (34.2 g, 1.2 eq.), and KOAc (31.5 g, 2.86 eq.) were placed in a round bottom flask and dissolved in anhydrous dioxane. dissolved. Afterwards, nitrogen gas was charged for 10 minutes, the mixture was stirred at room temperature, and the temperature of the oil container was raised from room temperature to 120°C. Afterwards, when the solvent began to boil, Pd(dppf)Cl 2 ·dichloromethane (8.2 g, 9 mol%) was added dropwise and stirred overnight. After the reaction, the organic layer was separated by washing with dichloromethane and water, water was removed with MgSO 4 , palladium was adsorbed with acidic clay and palladium charcoal, and the mixture was passed through a Celite pad. The passed solution was concentrated under reduced pressure and purified through column chromatography to obtain 23.3 g of intermediate compound A (yield 77%).
m/z [M]+ C16H19BO3 270.1m/z [M] + C 16 H 19 BO 3 270.1
단계 1-2: 중간체 화합물 C의 합성Step 1-2: Synthesis of Intermediate Compound C
상기 단계 1-1에서 제조한 화합물 A(23.2 g, 1.0 eq.), 화합물 B(39.7 g, 1.2 eq.)를 둥근 바닥 플라스크에 넣고 무수 테트라하이드로퓨란에 용해하였다. 이후, 10 분 동안 질소 가스를 충전 해주며 상온에서 교반하고, 2 M K2CO3(aq) (129 mL, 3.0 eq.)를 주입한 뒤, 오일 용기 온도를 상온에서 80℃로 올려주었다. 이후, 용매가 끓기 시작하면 Pd(PPh3)4(2.9 g, 3 mol%)를 적가 한 뒤, 하룻밤 동안 교반하였다. 반응 후, 디클로로메탄과 물로 수세하여 유기층을 분리하고, MgSO4로 물을 제거하고 산성백토, 팔라듐 차콜로 팔라듐을 흡착한 뒤 셀라이트 패드를 통과시켰다. 통과된 용액을 감압 하에 농축시킨 뒤, 얻어진 중간체 화합물 C를 정제하지 않고 혼합물 상태에서 다음 반응을 진행하였다. Compound A (23.2 g, 1.0 eq.) and Compound B (39.7 g, 1.2 eq.) prepared in step 1-1 were placed in a round bottom flask and dissolved in anhydrous tetrahydrofuran. Afterwards, nitrogen gas was charged for 10 minutes and stirred at room temperature, 2 MK 2 CO 3 (aq) (129 mL, 3.0 eq.) was injected, and the temperature of the oil container was raised from room temperature to 80°C. Afterwards, when the solvent began to boil, Pd(PPh 3 ) 4 (2.9 g, 3 mol%) was added dropwise and stirred overnight. After the reaction, the organic layer was separated by washing with dichloromethane and water, water was removed with MgSO 4 , palladium was adsorbed with acidic clay and palladium charcoal, and the mixture was passed through a Celite pad. After the passed solution was concentrated under reduced pressure, the obtained intermediate compound C was not purified and the next reaction was carried out in a mixture state.
m/z [M+H]+ C34H23O 447.3m/z [M+H] + C 34 H 23 O 447.3
단계 1-3: 중간체 화합물 D의 합성Step 1-3: Synthesis of Intermediate Compound D
상기 단계 1-2에서 제조한 혼합물 상태의 화합물 C(1.0 eq.)를 둥근 바닥 플라스크에 넣고 무수 디클로로메탄에 용해하였다. 이후, 피리딘(21.9 mL, 2.0 eq.)을 상온에서 적가한 뒤, 오일 용기 온도를 0℃로 낮춰 10분 동안 교반하였다. 이후, 무수 디클로로메탄에 용해한 Tf2O(21.5 g, 1.2 eq.)를 dropping funnel을 이용하여 천천히 혼합물에 적가하고, 오일 용기 온도를 서서히 0℃에서 상온으로 올려준 뒤, 하룻밤 동안 교반하였다. 반응 후, 용액을 감압 하에 농축시킨 뒤, 컬럼 크로마토그래피를 통해 정제하여 중간체 화합물 D 50 g (두 단계-수율 95%)을 얻었다. Compound C (1.0 eq.) prepared in step 1-2 was placed in a round bottom flask and dissolved in anhydrous dichloromethane. Afterwards, pyridine (21.9 mL, 2.0 eq.) was added dropwise at room temperature, and the temperature of the oil container was lowered to 0°C and stirred for 10 minutes. Afterwards, Tf 2 O (21.5 g, 1.2 eq.) dissolved in anhydrous dichloromethane was slowly added dropwise to the mixture using a dropping funnel, the temperature of the oil container was gradually raised from 0°C to room temperature, and the mixture was stirred overnight. After the reaction, the solution was concentrated under reduced pressure and purified through column chromatography to obtain 50 g of intermediate compound D (two steps - 95% yield).
m/z [M+H]+ C35H21F3O3S 579.3m/z [M+H] + C 35 H 21 F 3 O 3 S 579.3
단계 1-4: 중간체 화합물 E의 합성Step 1-4: Synthesis of intermediate compound E
상기 단계 1-3에서 제조한 화합물 D(7.0 g, 1.0 eq.), B2Pin2(6.1 g, 1.2 eq.) 및 KOAc(3.6 g, 3.0 eq.)를 둥근 바닥 플라스크에 넣고 무수 다이옥세인에 용해하였다. 이후, 10 분 동안 질소 가스를 충전해주며 상온에서 교반하고, 오일 용기 온도를 120℃로 올려주었다. 이후, 용매가 끓기 시작하면 Pd(dppf)Cl2·디클로로메탄(0.9 g, 9 mol%)을 적가 한 뒤, 하룻밤 동안 교반하였다. 반응 후, 디클로로메탄과 물로 수세하여 유기층을 분리하고, MgSO4로 물을 제거하고 산성백토, 팔라듐 차콜로 팔라듐을 흡착한 뒤 셀라이트 패드를 통과시켰다. 통과된 용액을 감압 하에 농축시킨 뒤, 컬럼 크로마토그래피를 통해 정제하여 중간체 화합물 E 6 g(수율 89%)을 얻었다. Compound D (7.0 g, 1.0 eq.), B 2 Pin 2 (6.1 g, 1.2 eq.) and KOAc (3.6 g, 3.0 eq.) prepared in steps 1-3 were added to a round bottom flask and added to anhydrous dioxane. dissolved in. Afterwards, nitrogen gas was charged for 10 minutes, the mixture was stirred at room temperature, and the temperature of the oil container was raised to 120°C. Afterwards, when the solvent began to boil, Pd(dppf)Cl 2 ·dichloromethane (0.9 g, 9 mol%) was added dropwise and stirred overnight. After the reaction, the organic layer was separated by washing with dichloromethane and water, water was removed with MgSO 4 , palladium was adsorbed with acidic clay and palladium charcoal, and the mixture was passed through a Celite pad. The passed solution was concentrated under reduced pressure and purified through column chromatography to obtain 6 g of intermediate compound E (yield 89%).
m/z [M+H]+ C40H43BO2 557.4m/z [M+H] + C 4 0H 43 B O 2 557.4
단계 1-5: 화합물 1의 합성Steps 1-5: Synthesis of Compound 1
상기 단계 1-3에서 제조한 화합물 E(1.5 g, 1.0 eq.) 및 화합물 F(1.7 g, 1.2 eq.)를 둥근 바닥 플라스크에 넣고 무수 테트라하이드로퓨란:톨루엔 (1:2)에 용해하였다. 10분 동안 질소 가스를 충전 해주며 상온에서 교반하고, 2 M K2CO3(aq) (4.0 mL, 3.0 eq.)를 주입한 뒤, 오일 용기 온도를 상온에서 120℃로 올려주었다. 이후, 용매가 끓기 시작하면 Pd(PPh3)4 (93 mg, 3 mol%)를 적가 한 뒤, 하룻밤 동안 교반하였다. 반응 후, 디클로로메탄과 물로 수세하여 유기층을 분리하고, MgSO4로 물을 제거하고 산성백토, 팔라듐 차콜로 팔라듐을 흡착한 뒤 셀라이트 패드를 통과시켰다. 통과된 용액을 감압 하에 농축시킨 뒤, 컬럼 크로마토그래피를 통해 정제하여 화합물 1 2 g(수율 92%)을 얻었고, 얻은 화합물 1의 MS Data를 도 3에 나타내었다. Compound E (1.5 g, 1.0 eq.) and Compound F (1.7 g, 1.2 eq.) prepared in steps 1-3 were placed in a round bottom flask and dissolved in anhydrous tetrahydrofuran:toluene (1:2). Nitrogen gas was charged for 10 minutes and stirred at room temperature, 2 MK 2 CO 3 (aq) (4.0 mL, 3.0 eq.) was injected, and the temperature of the oil container was raised from room temperature to 120°C. Afterwards, when the solvent began to boil, Pd(PPh 3 ) 4 (93 mg, 3 mol%) was added dropwise and stirred overnight. After the reaction, the organic layer was separated by washing with dichloromethane and water, water was removed with MgSO 4 , palladium was adsorbed with acidic clay and palladium charcoal, and the mixture was passed through a Celite pad. The passed solution was concentrated under reduced pressure and purified through column chromatography to obtain 2 g of Compound 1 (yield 92%). The MS data of Compound 1 is shown in Figure 3.
m/z [M+H]+ C64H50 809.6m/z [M+H] + C 64 H 50 809.6
제조예Manufacturing example 2: 화합물 2의 제조 2: Preparation of Compound 2
단계 2-1: 중간체 화합물 H의 합성Step 2-1: Synthesis of intermediate compound H
8-브로모나프탈렌-2-올(5.0 g, 1.0 eq.)을 둥근 바닥 플라스크에 넣고 무수 디클로로메탄에 용해하였다. 이후, 피리딘(3.6 mL, 2.0 eq.)을 상온에서 적가한 뒤, 오일 용기 온도를 0℃로 낮춰 10분 동안 교반하고, 무수 디클로로메탄에 용해한 Tf2O (4.5 mL, 1.2 eq.)를 dropping funnel을 이용하여 천천히 혼합물에 적가하였다. 이후, 오일 용기 온도를 서서히 0℃에서 상온으로 올려준 뒤, 하룻밤 동안 교반하였다. 반응 후, 용액을 감압 하에 농축시킨 뒤 컬럼 크로마토그래피를 통해 정제하여 중간체 화합물 H 8 g(수율 99%)을 얻었다.8-Bromonaphthalen-2-ol (5.0 g, 1.0 eq.) was added to a round bottom flask and dissolved in anhydrous dichloromethane. Afterwards, pyridine (3.6 mL, 2.0 eq.) was added dropwise at room temperature, the temperature of the oil container was lowered to 0°C, stirred for 10 minutes, and Tf 2 O (4.5 mL, 1.2 eq.) dissolved in anhydrous dichloromethane was dropped. It was slowly added dropwise to the mixture using a funnel. Afterwards, the temperature of the oil container was gradually raised from 0°C to room temperature, and then stirred overnight. After the reaction, the solution was concentrated under reduced pressure and purified through column chromatography to obtain 8 g of intermediate compound H (yield 99%).
m/z [M+H]+ C11H7BrF3O3S 354.8m/z [M+H] + C 11 H 7 BrF 3 O 3 S 354.8
단계 2-2: 중간체 화합물 I의 합성Step 2-2: Synthesis of Intermediate Compound I
상기 단계 2-1에서 제조한 화합물 H(2.88 g, 1.0 eq.), B2Pin2(8.24 g, 4.0 eq.), KOAc(4.78 g, 6.0 eq.)를 둥근 바닥 플라스크에 넣고 무수 다이옥세인에 용해하였다. 이후, 10분 동안 질소 가스를 충전해주며 상온에서 교반하고, 오일 용기 온도를 상온에서 120℃로 올려주었다. 이후, 용매가 끓기 시작하면 Pd(dppf)Cl2·디클로로메탄(1.2 g, 18 mol%)을 적가 한 뒤, 하룻밤 동안 교반하였다. 반응 후, 디클로로메탄과 물로 수세하여 유기층을 분리하고, MgSO4로 물을 제거하고 산성백토, 팔라듐 차콜로 팔라듐을 흡착한 뒤 셀라이트 패드를 통과시켰다. 통과된 용액을 감압 하에 농축시킨 뒤, 컬럼 크로마토그래피를 통해 정제하여 중간체 화합물 I 3 g(수율 97%)을 얻었다. Compound H (2.88 g, 1.0 eq.), B 2 Pin 2 (8.24 g, 4.0 eq.), and KOAc (4.78 g, 6.0 eq.) prepared in step 2-1 were added to a round bottom flask and added to anhydrous dioxane. dissolved in. Afterwards, nitrogen gas was charged for 10 minutes, the mixture was stirred at room temperature, and the temperature of the oil container was raised from room temperature to 120°C. Afterwards, when the solvent began to boil, Pd(dppf)Cl 2 ·dichloromethane (1.2 g, 18 mol%) was added dropwise and stirred overnight. After the reaction, the organic layer was separated by washing with dichloromethane and water, water was removed with MgSO 4 , palladium was adsorbed with acidic clay and palladium charcoal, and the mixture was passed through a Celite pad. The passed solution was concentrated under reduced pressure and purified through column chromatography to obtain 3 g of intermediate compound I (yield 97%).
m/z [M+H]+ C22H31B2O4 381.1m/z [M+H] + C 22 H 31 B 2 O 4 381.1
단계 2-3: 화합물 2의 합성Step 2-3: Synthesis of Compound 2
상기 단계 2-2에서 제조한 화합물 I(1.0 g, 1.0 eq.), 화합물 B(2.9 g, 2.4 eq.)를 둥근 바닥 플라스크에 넣고 무수 테트라하이드로퓨란:톨루엔 (1:2)에 용해하였다. 이후, 10분 동안 질소 가스를 충전 해주며 상온에서 교반하고, 2 M K2CO3(aq)(8 mL, 6.0 eq.)를 주입한 뒤, 오일 용기 온도를 상온에서 120℃로 올려주었다. 이후, 용매가 끓기 시작하면 Pd(PPh3)4(182.4 mg, 6 mol%)를 적가 한 뒤, 하룻밤 동안 교반하였다. 반응 후, 디클로로메탄과 물로 수세하여 유기층을 분리하고, MgSO4로 물을 제거하고 산성백토, 팔라듐 차콜로 팔라듐을 흡착한 뒤 셀라이트 패드를 통과시켰다. 통과된 용액을 감압 하에 농축시킨 뒤, 컬럼 크로마토그래피를 통해 정제하여 화합물 2 2 g(수율 85%)을 얻었고, 얻은 화합물 2의 MS Data를 도 4에 나타내었다. Compound I (1.0 g, 1.0 eq.) and Compound B (2.9 g, 2.4 eq.) prepared in step 2-2 were placed in a round bottom flask and dissolved in anhydrous tetrahydrofuran:toluene (1:2). Afterwards, nitrogen gas was charged for 10 minutes and stirred at room temperature, 2 MK 2 CO 3 (aq) (8 mL, 6.0 eq.) was injected, and the temperature of the oil container was raised from room temperature to 120°C. Afterwards, when the solvent began to boil, Pd(PPh 3 ) 4 (182.4 mg, 6 mol%) was added dropwise and stirred overnight. After the reaction, the organic layer was separated by washing with dichloromethane and water, water was removed with MgSO 4 , palladium was adsorbed with acidic clay and palladium charcoal, and the mixture was passed through a Celite pad. The passed solution was concentrated under reduced pressure and purified through column chromatography to obtain 2 g of Compound 2 (yield 85%), and the MS data of Compound 2 obtained is shown in Figure 4.
m/z [M+H]+ C58H37 733.6m/z [M+H] + C 58 H 37 733.6
실험예Experiment example 1: 용해도 실험 1: Solubility experiment
상기 제조예에서 제조한 화합물 1 및 2, 하기 화합물 X 및 Y를 각각 사이클로헥사논에 용해시켜 25℃에서의 용해도를 측정하였고, 그 결과를 표 1에 나타내었다.Compounds 1 and 2 prepared in the above Preparation Example and the following compounds
[화합물 X] [화합물 Y][Compound X] [Compound Y]
상기 표 1에 나타난 바와 같이, 본 발명의 상기 화학식 1로 표시되는 나프탈렌의 1번 및 7번 위치 모두에 안트라세닐기를 갖는 화합물은, 나프탈렌의 1번 위치에만 안트라세닐기를 갖는 비교 화합물 X와, 나프탈렌의 1번 및 4번 위치에 안트라세닐기를 갖는 비교 화합물 Y에 비하여 사이클로헥사논 용매에 대한 용해도가 현저히 높음을 알 수 있다.As shown in Table 1, the compound having an anthracenyl group at both the 1st and 7th positions of naphthalene represented by Formula 1 of the present invention is a comparative compound It can be seen that the solubility in cyclohexanone solvent is significantly higher than that of comparative compound Y, which has anthracenyl groups at positions 1 and 4.
실시예 1: 유기 발광 소자의 제조Example 1: Preparation of organic light emitting device
ITO(indium tin oxide)가 50 nm의 두께로 박막 코팅된 유리 기판을 세제를 녹인 증류수에 넣고 초음파로 세척하였다. 이때, 세제로는 피셔사(Fischer Co.) 제품을 사용하였으며, 증류수로는 밀리포어사(Millipore Co.) 제품의 필터(Filter)로 2차로 걸러진 증류수를 사용하였다. ITO를 30분간 세척한 후, 증류수로 2회 반복하여 초음파 세척을 10분간 진행하였다. 증류수 세척이 끝난 후, 이소프로필, 아세톤의 용제로 초음파 세척을 하고 건조시킨 후, 상기 기판을 5분간 세정한 후 글로브박스로 기판을 수송시켰다.A glass substrate coated with a thin film of indium tin oxide (ITO) to a thickness of 50 nm was placed in distilled water with a detergent dissolved in it and washed ultrasonically. At this time, a detergent from Fischer Co. was used, and distilled water filtered secondarily using a filter from Millipore Co. was used as distilled water. After washing the ITO for 30 minutes, ultrasonic cleaning was repeated twice with distilled water for 10 minutes. After washing with distilled water, ultrasonic cleaning was performed with isopropyl and acetone solvents, the substrate was dried, and the substrate was washed for 5 minutes before being transported to a glove box.
ITO 투명전극 위에, 하기 화합물 M 및 하기 화합물 L(8:2의 중량 비)의 2 wt/v% 톨루엔 코팅 조성물을 스핀 코팅(4000 rpm)하고 200℃에서 30분 동안 열처리(경화)하여 40 nm 두께로 정공주입층 형성하였다. 상기 정공주입층 위에 하기 화합물 K(Mn: 27,900; Mw: 35,600; Agilent 1200 series를 이용하여 PC 스텐다드(Standard)를 이용한 GPC로 측정)의 6 wt/v% 톨루엔 코팅 조성물을 스핀 코팅(4000 rpm)하고 200℃에서 30분 동안 열처리하여 20 nm 두께의 정공수송층을 형성하였다.On the ITO transparent electrode, a 2 wt/v% toluene coating composition of the following compound M and the following compound L (weight ratio of 8:2) was spin coated (4000 rpm) and heat treated (cured) at 200°C for 30 minutes to obtain a thickness of 40 nm. A hole injection layer was formed to a certain thickness. A 6 wt/v% toluene coating composition of the following compound K (Mn: 27,900; Mw: 35,600; measured by GPC using PC Standard using Agilent 1200 series) was spin coated (4000 rpm) on the hole injection layer. and heat treated at 200°C for 30 minutes to form a hole transport layer with a thickness of 20 nm.
상기 정공수송층 위에 상기 제조예 1에서 제조한 화합물 1과 하기 화합물 N (92:8의 중량 비)의 10 wt/v% 사이클로헥사논 코팅 조성물을 스핀 코팅(4000 rpm)하고 180℃에서 30분 동안 열처리하여 400 Å 두께로 발광층을 형성하였다. 진공 증착기로 이송한 후, 상기 발광층 위에 하기 화합물 O를 35 nm의 두께로 진공 증착하여 전자 주입 및 수송층을 형성하였다. 상기 전자 주입 및 수송층 위에 순차적으로 1 nm 두께로 LiF와 100 nm 두께로 알루미늄을 증착하여 캐소드를 형성하였다.On the hole transport layer, a 10 wt/v% cyclohexanone coating composition of Compound 1 prepared in Preparation Example 1 and Compound N (weight ratio of 92:8) was spin coated (4000 rpm) for 30 minutes at 180°C. Heat treatment was performed to form a light emitting layer with a thickness of 400 Å. After being transferred to a vacuum evaporator, the following compound O was vacuum deposited on the light emitting layer to a thickness of 35 nm to form an electron injection and transport layer. A cathode was formed by sequentially depositing LiF to a thickness of 1 nm and aluminum to a thickness of 100 nm on the electron injection and transport layer.
상기의 과정에서 유기물의 증착 속도는 0.4 내지 0.7 Å /sec를 유지하였고, LiF는 0.3 Å/sec, 알루미늄은 2 Å /sec의 증착 속도를 유지하였으며, 증착 시 진공도는 2 × 10-7 내지 5 × 10-8 torr를 유지하였다.In the above process, the deposition rate of organic materials was maintained at 0.4 to 0.7 Å/sec, LiF was maintained at 0.3 Å/sec, and aluminum was maintained at 2 Å/sec, and the vacuum degree during deposition was 2 × 10 -7 to 5. × 10 -8 torr was maintained.
실시예Example 2, 2, 비교예Comparative example 1 및 1 and 비교예Comparative example 2 2
발광층의 호스트로 화합물 1 대신 하기 표 2에 기재된 화합물을 사용하는 것을 제외하고는, 상기 실시예 1과 동일한 방법으로 유기 발광 소자를 제조하였다. An organic light-emitting device was manufactured in the same manner as Example 1, except that the compounds listed in Table 2 below were used as the host of the light-emitting layer instead of Compound 1.
실험예Experiment example 2: 유기 발광 소자 특성 평가 2: Evaluation of organic light emitting device characteristics
상기 실시예 1, 실시예 2, 비교예 1 및 비교예 2에서 제조한 유기 발광 소자에 전류를 인가하였을 때, 10 mA/cm2의 전류 밀도에서의 구동 전압, 외부 양자 효율(external quantum efficiency, EQE), 휘도 및 수명을 측정한 결과를 하기 표 2에 나타내었다. 이때, 외부양자효율(EQE)은 (방출된 광자 수)/(주입된 전하운반체 수)로 구하였고, T90는 휘도가 초기 휘도(500 nit)에서 90%로 감소되는데 소요되는 시간을 의미한다.When current was applied to the organic light emitting device manufactured in Example 1, Example 2, Comparative Example 1, and Comparative Example 2, the driving voltage and external quantum efficiency (external quantum efficiency) at a current density of 10 mA/cm 2 The results of measuring EQE), luminance, and lifespan are shown in Table 2 below. At this time, the external quantum efficiency (EQE) was calculated as (number of photons emitted)/(number of injected charge carriers), and T90 refers to the time required for the brightness to decrease to 90% from the initial brightness (500 nits).
(발광층 호스트)compound
(Emissive layer host)
(V
@10mA/cm2) driving voltage
(V
@10mA/cm 2 )
(%
@10mA/cm2)EQE
(%
@10mA/cm 2 )
(T90
@500 nit)Lifespan (hr)
(T90
@500 nits)
상기 표 2에 나타난 바와 같이, 본 발명의 화합물을 발광층의 호스트로 사용한 유기 발광 소자는, 비교예 화합물 X 및 Y를 발광층의 호스트로 사용한 유기 발광 소자에 비하여, 수명 측면에서 매우 우수한 특성을 나타냄을 알 수 있다.As shown in Table 2, the organic light-emitting device using the compound of the present invention as the host of the light-emitting layer shows very excellent characteristics in terms of lifespan compared to the organic light-emitting device using Comparative Example compounds X and Y as the host of the light-emitting layer. Able to know.
1: 기판 2: 양극
3: 발광층 4: 음극
5: 정공주입층 6: 정공수송층
7: 발광층 8: 전자주입 및 수송층1: Substrate 2: Anode
3: light emitting layer 4: cathode
5: hole injection layer 6: hole transport layer
7: Light-emitting layer 8: Electron injection and transport layer
Claims (7)
[화학식 1]
상기 화학식 1에서,
L1 및 L2는 각각 독립적으로, 단일결합, 1,3-페닐렌, 또는 1,4-페닐렌이고,
Ar1 및 Ar2는 각각 독립적으로, 비치환되거나, 또는 1개 또는 2개의 C1-10 알킬로 치환된 C6-20 아릴이다.
Compound represented by Formula 1:
[Formula 1]
In Formula 1,
L 1 and L 2 are each independently a single bond, 1,3-phenylene, or 1,4-phenylene,
Ar 1 and Ar 2 are each independently C 6-20 aryl that is unsubstituted or substituted with 1 or 2 C 1-10 alkyl.
Ar1 및 Ar2는 각각 독립적으로, 하기로 구성되는 군으로부터 선택되는 어느 하나인, 화합물:
According to paragraph 1,
Ar 1 and Ar 2 are each independently any one selected from the group consisting of:
L1 및 L2가 서로 동일하고, Ar1 및 Ar2가 서로 동일하거나;
L1 및 L2는 서로 상이하고, Ar1 및 Ar2가 서로 동일하거나; 또는
L1 및 L2가 서로 상이하고, Ar1 및 Ar2가 서로 상이한,
화합물.
According to paragraph 1,
L 1 and L 2 are the same as each other, and Ar 1 and Ar 2 are the same as each other;
L 1 and L 2 are different from each other and Ar 1 and Ar 2 are the same as each other; or
L 1 and L 2 are different from each other, Ar 1 and Ar 2 are different from each other,
compound.
상기 화합물은 하기 화합물로 구성되는 군으로부터 선택되는 어느 하나인, 화합물:
According to paragraph 1,
The compound is any one selected from the group consisting of the following compounds:
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