KR102630138B1 - 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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- KR102630138B1 KR102630138B1 KR1020190027743A KR20190027743A KR102630138B1 KR 102630138 B1 KR102630138 B1 KR 102630138B1 KR 1020190027743 A KR1020190027743 A KR 1020190027743A KR 20190027743 A KR20190027743 A KR 20190027743A KR 102630138 B1 KR102630138 B1 KR 102630138B1
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- compound
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- organic light
- emitting device
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- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
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- 235000011187 glycerol Nutrition 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
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- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005549 heteroarylene group Chemical group 0.000 description 1
- FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 description 1
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- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- 238000002156 mixing Methods 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 239000007773 negative electrode material Substances 0.000 description 1
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical group [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
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- 229910052763 palladium Inorganic materials 0.000 description 1
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- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 150000002987 phenanthrenes Chemical class 0.000 description 1
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 description 1
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
- XPPWLXNXHSNMKC-UHFFFAOYSA-N phenylboron Chemical group [B]C1=CC=CC=C1 XPPWLXNXHSNMKC-UHFFFAOYSA-N 0.000 description 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 229920000123 polythiophene Polymers 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- JCBJVAJGLKENNC-UHFFFAOYSA-N potassium;ethoxymethanedithioic acid Chemical compound [K+].CCOC(S)=S JCBJVAJGLKENNC-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 150000003220 pyrenes Chemical class 0.000 description 1
- 125000001725 pyrenyl group Chemical group 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical group C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
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- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 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
- 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
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 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
- 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
- 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
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 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
- 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
- 238000004506 ultrasonic cleaning 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
- 238000005406 washing Methods 0.000 description 1
- 125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
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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 is 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,
R1 및 R2는 각각 독립적으로, 치환 또는 비치환된 C1-60 알킬; 또는 치환 또는 비치환된 C6-60 아릴이고,R 1 and R 2 are each independently substituted or unsubstituted C 1-60 alkyl; Or substituted or unsubstituted C 6-60 aryl,
L1 및 L2는 각각 독립적으로, 치환 또는 비치환된 C6-60 아릴렌이고,L 1 and L 2 are each independently substituted or unsubstituted C 6-60 arylene,
Ar1 내지 Ar6는 각각 독립적으로, 치환 또는 비치환된 C6-60 아릴이다. Ar 1 to Ar 6 are each independently substituted or unsubstituted C 6-60 aryl.
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 Formula 1 described above can be used as a material for the organic layer of an organic light-emitting device, can also be used in a solution process, and can improve efficiency, low driving voltage, and/or lifespan characteristics in an organic light-emitting device. 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), 전자수송층(8), 전자주입층(9) 및 음극(4)으로 이루어진 유기 발광 소자의 예를 도시한 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 shows a substrate (1), an anode (2), a hole injection layer (5), a hole transport layer (6), a light emitting layer (7), an electron transport layer (8), an electron injection layer (9), and a cathode (4). An example of an organic light emitting device is shown.
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, 및 는 다른 치환기에 연결되는 결합을 의미하고, Ph는 페닐기를 의미한다.In this specification, and means a bond connected to another substituent, and Ph means a phenyl group.
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 the present 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 또는 분지쇄일 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, 사이클로헥실메틸, 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 or 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 잔텐(xanthene), 티오잔텐(thioxanthen), 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 xanthene, thioxanthen, 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 ( phenanthroline), isoxazolyl group, thiadiazolyl group, phenothiazinyl group, and dibenzofuranyl group, etc., but is 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)
본 발명은 상기 화학식 1로 표시되는 디아민 화합물을 제공한다. The present invention provides a diamine compound represented by Formula 1 above.
상기 화학식 1로 표시되는 화합물은, 벤조플루오렌 코어 양쪽에 아미노기가 연결되어 있고, 상기 아미노기는 디벤조퓨라닐기와 트리아릴실릴기로 치환되어 있는 구조를 갖는다. 이와 같이, bulky한 치환기인 트리아릴실릴기로 치환된 아미노기를 갖는 상기 화학식 1로 표시되는 화합물은, 트리알킬실릴기, 디알킬아릴실릴기 또는 알킬디아릴실릴기로 치환된 아미노기를 갖는 화합물에 비하여, 분자간의 π- π 상호작용(π-ð interaction)이 약해져서 용액 공정에 사용되는 유기 용매에 대한 용해도가 높을 수 있다. 또한, 상기 화학식 1로 표시되는 화합물은 높은 유리전이온도를 가져 용액 공정 후 형성되는 막 특성이 향상되어, 상기 화합물을 채용한 유기 발광 소자의 효율 및 수명 특성이 향상될 수 있다.The compound represented by Formula 1 has an amino group connected to both sides of the benzofluorene core, and the amino group is substituted with a dibenzofuranyl group and a triarylsilyl group. In this way, the compound represented by Formula 1 having an amino group substituted with a triarylsilyl group, which is a bulky substituent, is compared to a compound having an amino group substituted with a trialkylsilyl group, dialkylarylsilyl group, or alkyldiarylsilyl group, The π-π interaction between molecules may be weakened, resulting in high solubility in organic solvents used in the solution process. In addition, the compound represented by Formula 1 has a high glass transition temperature, which improves the characteristics of the film formed after the solution process, so that the efficiency and lifespan characteristics of the organic light-emitting device employing the compound can be improved.
따라서, 상기 화학식 1로 표시되는 화합물은 용액 공정에 사용되는 유기 용매, 예를 들어 톨루엔과 같은 용매에 대한 용해도가 높고, 높은 유리전이온도를 가져 경화 후 용매에 대한 내성이 뛰어나므로, 용액 공정에 사용이 적합하다.Therefore, the compound represented by Formula 1 has high solubility in organic solvents used in the solution process, such as toluene, and has a high glass transition temperature and excellent resistance to solvents after curing, so it can be used in the solution process. It is suitable for use.
바람직하게는, 상기 화학식 1에서, R1 및 R2는 각각 독립적으로 C1-10 알킬 또는 C6-20 아릴이다. 이때, R1 및 R2는 서로 동일할 수 있다.Preferably, in Formula 1, R 1 and R 2 are each independently C 1-10 alkyl or C 6-20 aryl. At this time, R 1 and R 2 may be the same.
보다 바람직하게는, R1 및 R2는 각각 독립적으로, 메틸, 또는 페닐이다.More preferably, R 1 and R 2 are each independently methyl or phenyl.
바람직하게는, L1 및 L2는 각각 독립적으로, 비치환되거나, 또는 할로겐 또는 시아노로 치환된 C6-20 아릴렌이다.Preferably, L 1 and L 2 are each independently C 6-20 arylene, which is unsubstituted or substituted with halogen or cyano.
보다 바람직하게는, L1 및 L2는 각각 독립적으로, 비치환되거나, 또는 할로겐 또는 시아노로 치환된 페닐렌; 또는 비치환되거나, 또는 할로겐 또는 시아노로 치환된 비페닐디일이다.More preferably, L 1 and L 2 are each independently phenylene unsubstituted or substituted with halogen or cyano; Or it is unsubstituted, or biphenyldiyl substituted with halogen or cyano.
가장 바람직하게는, L1 및 L2는 각각 독립적으로, 하기로 구성되는 군으로부터 선택되는 어느 하나이다:Most preferably, L 1 and L 2 are each independently selected from the group consisting of:
상기에서,In the above,
Z1 내지 Z3는 각각 독립적으로, 수소, 플루오로, 또는 시아노이다.Z 1 to Z 3 are each independently hydrogen, fluoro, or cyano.
예를 들어, Z1 및 Z2 모두 수소이거나; 또는 Z1 및 Z2 중 하나는 수소이고, 다른 하나는 플루오로, 또는 시아노이고, Z3는 수소이다.For example, both Z 1 and Z 2 are hydrogen; or one of Z 1 and Z 2 is hydrogen, the other is fluoro, or cyano, and Z 3 is hydrogen.
이때, L1 및 L2는 서로 동일할 수 있다.At this time, L 1 and L 2 may be the same.
바람직하게는, Ar1 내지 Ar6는 각각 독립적으로, 비치환되거나, 또는 C1-4 알킬로 치환된 C6-20 아릴이다. 보다 바람직하게는, Ar1 및 Ar4가 서로 동일하고, Ar2 및 Ar5가 서로 동일하고, Ar3 및 Ar6가 서로 동일할 수 있다. Preferably, Ar 1 to Ar 6 are each independently C 6-20 aryl unsubstituted or substituted with C 1-4 alkyl. More preferably, Ar 1 and Ar 4 may be the same as each other, Ar 2 and Ar 5 may be the same as each other, and Ar 3 and Ar 6 may be the same as each other.
가장 바람직하게는, Ar1 내지 Ar6는 서로 동일하다. 예를 들어, Ar1 내지 Ar6는 모두 페닐이거나; 또는 Ar1 내지 Ar6는 모두 4-메틸페닐이다. Most preferably, Ar 1 to Ar 6 are identical to each other. For example, Ar 1 to Ar 6 are all phenyl; Or Ar 1 to Ar 6 are all 4-methylphenyl.
또한, 상기 화학식 1로 표시되는 화합물은 2개의 아미노기 내 디벤조퓨라닐이 질소 원자와 결합되는 위치가 서로 동일한 경우, 그 결합되는 위치에 따라 하기 화학식 1A 내지 1D 중 어느 하나로 표시될 수 있다:In addition, the compound represented by Formula 1 may be represented by any one of the following Formulas 1A to 1D depending on the bonding position when the positions at which the dibenzofuranyl in the two amino groups is bonded to the nitrogen atom are the same:
[화학식 1A][Formula 1A]
[화학식 1B][Formula 1B]
[화학식 1C][Formula 1C]
[화학식 1D][Formula 1D]
상기 화학식 1A 내지 1D에서,In Formulas 1A to 1D,
R1, R2, L1, L2 및 Ar1 내지 Ar6는 상기 화학식 1에서 정의한 바와 같다.R 1 , R 2 , L 1 , L 2 and Ar 1 to Ar 6 are as defined in Formula 1 above.
바람직하게는, 상기 화합물은 하기 화학식 1-1 또는 1-2로 표시된다:Preferably, the compound is represented by the formula 1-1 or 1-2:
[화학식 1-1][Formula 1-1]
[화학식 1-2][Formula 1-2]
상기 화학식 1-1 및 1-2에서,In Formulas 1-1 and 1-2,
R1, R2, L1 및 L2는 상기 화학식 1에서 정의한 바와 같고,R 1 , R 2 , L 1 and L 2 are as defined in Formula 1 above,
Z는 각각 독립적으로, 수소, 또는 메틸이다. Z is each independently hydrogen or methyl.
보다 바람직하게는, 상기 화학식 1-1 및 1-2에서,More preferably, in Formulas 1-1 and 1-2,
R1 및 R2는 모두 메틸이거나; 또는 모두 페닐이고,R 1 and R 2 are both methyl; or all are phenyl,
L1 및 L2는 서로 동일하고, 비치환되거나, 또는 할로겐 또는 시아노로 치환된 C6-20 아릴렌이고,L 1 and L 2 are the same as each other and are unsubstituted or C 6-20 arylene substituted with halogen or cyano,
Z는 모두 수소이거나; 또는 모두 메틸이다. Z is all hydrogen; or are all methyl.
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 L1 및 L2가 서로 동일하고, Ar1 및 Ar4가 서로 동일하고, Ar2 및 Ar5가 서로 동일하고, Ar3 및 Ar6가 서로 동일한 경우에, 하기 반응식 1과 같은 제조 방법으로 제조할 수 있다. On the other hand, the compound represented by Formula 1 is, for example, L 1 and L 2 are the same as each other, Ar 1 and Ar 4 are the same as each other, Ar 2 and Ar 5 are the same as each other, and Ar 3 and Ar 6 are the same as each other. In this case, it can be manufactured by the manufacturing method shown in Scheme 1 below.
[반응식 1][Scheme 1]
상기 반응식 1에서, 각 치환기에 대한 정의는 앞서 설명한 바와 동일하다. 상기 단계 1은, 1차 아민 화합물 A-2에 출발물질 A-1을 반응시켜 2차 아민인 중간체 화합물 A-3을 제조하는 단계이고, 상기 단계 2는 화합물 A-4의 2개의 반응 사이트에 중간체 화합물 A-3의 아미노기를 도입하여 화학식 1로 표시되는 화합물을 제조하는 단계이다. 상기 단계 1-1 및 1-2는 모두 팔라듐 촉매 하에 수행되는 것이 바람직하며, 이러한 제조 방법은 후술할 제조예에서 보다 구체화될 수 있다. In Scheme 1, the definition of each substituent is the same as previously described. Step 1 is a step of preparing intermediate compound A-3, a secondary amine, by reacting starting material A-1 with primary amine compound A-2, and step 2 is a step of preparing intermediate compound A-3, which is a secondary amine, at two reaction sites of compound A-4. This is the step of preparing the compound represented by Formula 1 by introducing the amino group of intermediate compound A-3. It is preferable that steps 1-1 and 1-2 are both performed under a palladium catalyst, and this manufacturing method can be further detailed in the manufacturing examples to be 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 도펀트 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 dopant 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. 바람직하게는 상기 용매로 톨루엔을 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. Preferably, toluene can be used as the solvent.
또한, 상기 코팅 조성물은 호스트 재료로 사용되는 화합물을 더 포함할 수 있고, 상기 호스트 재료에 사용되는 화합물에 대한 설명은 후술한다.In addition, the coating composition may further include a compound used as a host material, and a description of the compound used as the host material will be described later.
또한, 상기 코팅 조성물의 점도는 1 cP 내지 10 cP가 바람직하며, 상기의 범위에서 코팅이 용이하다. 또한, 상기 코팅 조성물 내 본 발명에 따른 화합물의 농도는 0.1 wt% 내지 20 wt%인 것이 바람직하다. Additionally, the viscosity of the coating composition is preferably 1 cP to 10 cP, and coating is easy within this range. In addition, the concentration of the compound according to the present invention in the coating composition is preferably 0.1 wt% to 20 wt%.
바람직하게는, 상기 코팅 조성물의 용매에 대한 용해도(wt%)는 용매 톨루엔을 기준으로 1 wt% 내지 20 wt%이고, 이에 따라 상기 화학식 1로 표시되는 화합물을 포함하는 코팅 조성물은 용액 공정에 사용되기 적합하다.Preferably, the solubility (wt%) of the coating composition in the solvent is 1 wt% to 20 wt% based on the solvent toluene, and accordingly, the coating composition containing the compound represented by Formula 1 is used in the solution process. suitable to become
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 100 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 100 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 including 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, 상기 제1 전극이 양극이고 상기 제2 전극은 음극인, 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, 상기 제1 전극이 음극이고 상기 제2 전극은 양극인, 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.In addition, the organic light emitting device according to the present invention is 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 where the first electrode is an anode and the second electrode is a cathode. It may be a device. In addition, the organic light emitting device according to the present invention is an inverted type organic device in which a cathode, one or more organic material layers, and an anode are sequentially stacked on a substrate where the first electrode is a cathode and the second electrode is an anode. It may be a light emitting device. 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), 전자수송층(8), 전자주입층(9) 및 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 2 shows a substrate (1), an anode (2), a hole injection layer (5), a hole transport layer (6), a light emitting layer (7), an electron transport layer (8), an electron injection layer (9), and a cathode (4). An example of an organic light emitting device is shown. 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 PVD (physical vapor deposition) 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.
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 multi-layer structure materials such as LiF/Al or LiO 2 /Al, but they are not limited to these.
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 발광층은 호스트 재료 및 도펀트 재료를 포함할 수 있다. 도펀트 재료로는 상술한 화학식 1로 표시되는 화합물이 사용될 수 있다. 또한, 호스트 재료로는 축합 방향족환 유도체 또는 헤테로환 함유 화합물 등을 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 a dopant material, a compound represented by the above-mentioned formula (1) may be used. Additionally, as the host material, a condensed aromatic ring derivative or a heterocyclic ring-containing compound can be used. Specifically, condensed aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, and fluoranthene compounds, and heterocycle-containing compounds include carbazole derivatives, dibenzofuran derivatives, and ladder-type compounds. These include, but are not limited to, furan compounds and pyrimidine derivatives.
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. 또는 플루오레논, 안트라퀴노다이메탄, 다이페노퀴논, 티오피란 다이옥사이드, 옥사졸, 옥사다이아졸, 트리아졸, 이미다졸, 벤즈이미다졸, 페릴렌테트라카복실산, 프레오레닐리덴 메탄, 안트론 등과 그들의 유도체, 금속 착체 화합물, 또는 질소 함유 5원환 유도체 등을 사용할 수도 있으나, 이들에만 한정되는 것은 아니다. 상기 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. or fluorenone, anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, benzimidazole, perylenetetracarboxylic acid, preorenylidene methane, anthrone, etc. and their derivatives. , metal complex compounds, or nitrogen-containing 5-membered ring derivatives may be used, 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
제조예Manufacturing example 1: 화합물 BD105의 합성 1: Synthesis of compound BD105
단계 1-1: 중간체 화합물 1-B의 합성Step 1-1: Synthesis of intermediate compound 1-B
출발물질 1-A(10 g, 24.15 mmol), 4-아미노디벤조퓨란(4-aminodibenzofuran)(4.86 g, 26.57 mmol), 및 소듐터트부톡사이드(NaOt-Bu) (3.48 g, 36.23 mmol)을 250 ml 둥근 바닥 플라스크에 넣어주었다. 질소 조건에서 Toluene 100 ml를 넣고 100℃까지 온도를 올렸다. Pd(P(t-Bu3))2(123 mg, 0.24 mmol)을 둥근 바닥 플라스크에 넣어주고 빛을 차단한 뒤 2시간동안 교반하였다. 온도를 낮추고 디클로로메탄(DCM: Dichloromethane)과 물을 이용하여 물질을 추출한 후, MgSO4와 산성백토를 넣고 교반 하였다. 실리카겔에 통과시킨 후 용매를 제거하였다. 이후, 컬럼 크로마토그래피(Dichloromethane/Hexane)를 통해 중간체 화합물 1-B를 분리하였다.Starting materials 1-A (10 g, 24.15 mmol), 4-aminodibenzofuran (4.86 g, 26.57 mmol), and sodium tertbutoxide (NaOt-Bu) (3.48 g, 36.23 mmol) It was placed in a 250 ml round bottom flask. Under nitrogen conditions, 100 ml of toluene was added and the temperature was raised to 100°C. Pd(P(t-Bu 3 )) 2 (123 mg, 0.24 mmol) was added to a round bottom flask, blocked from light, and stirred for 2 hours. After lowering the temperature and extracting the substance using dichloromethane (DCM) and water, MgSO 4 and acidic clay were added and stirred. After passing through silica gel, the solvent was removed. Afterwards, intermediate compound 1-B was separated through column chromatography (Dichloromethane/Hexane).
단계 1-2: 화합물 BD105의 합성Step 1-2: Synthesis of compound BD105
상기 단계 1-1에서 제조한 중간체 화합물 1-B(3 g, 5.8 mmol), 화합물 1-C (1.054g, 2.64mmol), 및 소듐터트부톡사이드(NaOt-Bu)(760 mg, 7.9 mmol)을 250 ml 둥근 바닥 플라스크에 넣어주었다. 질소 조건에서 Toluene 100 ml를 넣고 100℃까지 온도를 올렸다. Pd(P(tBu3))2(26.95 mg, 0.05 mmol)을 둥근 바닥 플라스크에 넣어주고 빛을 차단한 뒤 2시간 동안 교반 하였다. 온도를 낮추고 디클로로메탄(DCM: Dichloromethane)과 물을 이용하여 물질을 추출한 후, MgSO4와 산성백토를 넣고 교반하였다. 실리카겔에 통과시킨 후 용매를 제거하였다. 이후, 컬럼 크로마토그래피(Dichloromethane/Hexane)를 통해 화합물 BD105(1.4 g, 수율: 42%)를 분리하였다. Intermediate compound 1-B (3 g, 5.8 mmol), compound 1-C (1.054 g, 2.64 mmol), and sodium tert-butoxide (NaOt-Bu) (760 mg, 7.9 mmol) prepared in step 1-1. was placed in a 250 ml round bottom flask. Under nitrogen conditions, 100 ml of toluene was added and the temperature was raised to 100°C. Pd(P(tBu 3 )) 2 (26.95 mg, 0.05 mmol) was added to a round bottom flask, blocked from light, and stirred for 2 hours. After lowering the temperature and extracting the substance using dichloromethane (DCM) and water, MgSO 4 and acidic clay were added and stirred. After passing through silica gel, the solvent was removed. Afterwards, compound BD105 (1.4 g, yield: 42%) was isolated through column chromatography (Dichloromethane/Hexane).
MS (LC-MS) : 1274.47 m/z [M+]MS (LC-MS): 1274.47 m/z [M + ]
제조예Manufacturing example 2: 화합물 BD106의 합성 2: Synthesis of compound BD106
상기 제조예 1의 단계 1-1에서 출발물질 1-A 대신 출발물질 2-A를 사용한 것을 제외하고는, 상기 제조예 1과 동일한 방법을 사용하여, 화합물 BD106(1.5 g, 수율: 45%)을 얻었다.Using the same method as Preparation Example 1, except that starting material 2-A was used instead of starting material 1-A in step 1-1 of Preparation Example 1, compound BD106 (1.5 g, yield: 45%) got it
MS (LC-MS) : 1274.47 m/z [M+]MS (LC-MS): 1274.47 m/z [M + ]
제조예Manufacturing example 3: 화합물 BD1의 합성 3: Synthesis of compound BD1
단계 3-1: 중간체 화합물 3-B의 합성Step 3-1: Synthesis of intermediate compound 3-B
출발물질 3-A(10 g, 20.4 mmol), 4-아미노디벤조퓨란(4-aminodibenzofuran) (4.11 g, 22.44 mmol), 및 소듐터트부톡사이드(NaOt-Bu) (2.9 g, 30.6 mmol)을 250 ml 둥근 바닥 플라스크에 넣어주었다. 질소 조건에서 Toluene 100 ml를 넣고 100℃까지 온도를 올렸다. Pd(P(tBu3))2 (104.28 mg, 0.134 mmol)을 둥근 바닥 플라스크에 넣어주고 빛을 차단한 뒤 2시간동안 교반 하였다. 온도를 낮추고 디클로로메탄(DCM)과 물을 이용하여 물질을 추출한 후, MgSO4와 산성백토를 넣고 교반 하였다. 실리카겔에 통과시킨 후 용매를 제거하였다. 이후, 컬럼 크로마토그래피(Dichloromethane/Hexane)를 통해 중간체 3-B를 분리하였다.Starting materials 3-A (10 g, 20.4 mmol), 4-aminodibenzofuran (4.11 g, 22.44 mmol), and sodium tertbutoxide (NaOt-Bu) (2.9 g, 30.6 mmol) It was placed in a 250 ml round bottom flask. Under nitrogen conditions, 100 ml of toluene was added and the temperature was raised to 100°C. Pd(P(tBu 3 )) 2 (104.28 mg, 0.134 mmol) was added to a round bottom flask, blocked from light, and stirred for 2 hours. After lowering the temperature and extracting the material using dichloromethane (DCM) and water, MgSO 4 and acidic clay were added and stirred. After passing through silica gel, the solvent was removed. Afterwards, intermediate 3-B was separated through column chromatography (Dichloromethane/Hexane).
단계 3-2: 화합물 BD1의 합성Step 3-2: Synthesis of compound BD1
상기 단계 3-1에서 제조한 중간체 화합물 3-B(3 g, 5.06 mmol), 중간체 1-C (919 mg, 2.3 mmol), 및 소듐터트부톡사이드(NaOt-Bu)(662.7 mg, 6.9 mmol) 을 250 ml 둥근 바닥 플라스크에 넣어주었다. 질소 조건에서 Toluene 100 ml를 넣고 100℃까지 온도를 올렸다. Pd(P(tBu3))2(23.5 mg, 0.046 mmol)을 둥근 바닥 플라스크에 넣어주고 빛을 차단한 뒤 2시간동안 교반 하였다. 온도를 낮추고 디클로로메탄(DCM)과 물을 이용하여 물질을 추출한 후, MgSO4와 산성백토를 넣고 교반 하였다. 실리카겔에 통과시킨 후 용매를 제거하였다. 컬럼 크로마토그래피(Dichloromethane/Hexane)를 통해 화합물 BD1(1.2 g, 수율: 37%)을 분리하였다. Intermediate compound 3-B (3 g, 5.06 mmol), intermediate 1-C (919 mg, 2.3 mmol), and sodium tert-butoxide (NaOt-Bu) (662.7 mg, 6.9 mmol) prepared in step 3-1. was placed in a 250 ml round bottom flask. Under nitrogen conditions, 100 ml of toluene was added and the temperature was raised to 100°C. Pd(P(tBu 3 )) 2 (23.5 mg, 0.046 mmol) was added to a round bottom flask, blocked from light, and stirred for 2 hours. After lowering the temperature and extracting the material using dichloromethane (DCM) and water, MgSO 4 and acidic clay were added and stirred. After passing through silica gel, the solvent was removed. Compound BD1 (1.2 g, yield: 37%) was isolated through column chromatography (Dichloromethane/Hexane).
MS (LC-MS) : 1426.53 m/z [M+]MS (LC-MS): 1426.53 m/z [M + ]
제조예Manufacturing example 4: 화합물 BD8의 합성 4: Synthesis of compound BD8
단계 4-1: 중간체 화합물 4-B의 합성Step 4-1: Synthesis of intermediate compound 4-B
출발물질 4-A(10 g, 20.4 mmol), 4-아미노디벤조퓨란(4-aminodibenzofuran) (4.11 g, 22.44 mmol), 및 소듐터트부톡사이드(NaOt-Bu) (2.94g, 30.6mmol 을 250 ml 둥근 바닥 플라스크에 넣어주었다. 질소 조건에서 Toluene 100 ml를 넣고 100℃까지 온도를 올렸다. Pd(P(tBu3))2(104.3 mg, 0.204 mmol)을 둥근 바닥 플라스크에 넣어주고 빛을 차단한 뒤 2시간동안 교반 하였다. 온도를 낮추고 디클로로메탄(DCM)과 물을 이용하여 물질을 추출한 후, MgSO4와 산성백토를 넣고 교반 하였다. 실리카겔에 통과시킨 후 용매를 제거하였다. 컬럼 크로마토그래피(methyl chloride/Hexane)를 통해 중간체 4-B를 분리하였다.Starting materials 4-A (10 g, 20.4 mmol), 4-aminodibenzofuran (4.11 g, 22.44 mmol), and sodium tertbutoxide (NaOt-Bu) (2.94 g, 30.6 mmol) were dissolved in 250 ml was placed in a round bottom flask. Under nitrogen conditions, 100 ml of Toluene was added and the temperature was raised to 100°C. Pd(P(tBu 3 )) 2 (104.3 mg, 0.204 mmol) was added to the round bottom flask and light was blocked. It was then stirred for 2 hours. The temperature was lowered and the material was extracted using dichloromethane (DCM) and water, then MgSO 4 and acidic clay were added and stirred. After passing through silica gel, the solvent was removed. Column chromatography (methyl Intermediate 4-B was isolated through chloride/hexane).
단계 4-2: 화합물 BD8의 합성Step 4-2: Synthesis of compound BD8
상기 단계 4-1에서 제조한 중간체 화합물 4-B(3 g, 5.06 mmol), 중간체 1-C(919 mg, 2.3 mmol), 및 소듐터트부톡사이드(NaOt-Bu)(662 mg, 6.9 mmol)을 250 ml 둥근 바닥 플라스크에 넣어주었다. 질소 조건에서 Toluene 100 ml를 넣고 100℃까지 온도를 올렸다. Pd(P(tBu3))2(23.5 mg, 0.04 mmol)을 둥근 바닥 플라스크에 넣어주고 빛을 차단한 뒤 2시간동안 교반 하였다. 온도를 낮추고 디클로로메탄(DCM)과 물을 이용하여 물질을 추출한 후, MgSO4와 산성백토를 넣고 교반 하였다. 실리카겔에 통과시킨 후 용매를 제거하였다. 컬럼 크로마토그래피(Dichloromethane/Hexane)를 통해 화합물 BD-8(1.38 g, 수율: 42%)를 분리하였다. Intermediate compound 4-B (3 g, 5.06 mmol), intermediate 1-C (919 mg, 2.3 mmol), and sodium tert-butoxide (NaOt-Bu) (662 mg, 6.9 mmol) prepared in step 4-1. was placed in a 250 ml round bottom flask. Under nitrogen conditions, 100 ml of toluene was added and the temperature was raised to 100°C. Pd(P(tBu 3 )) 2 (23.5 mg, 0.04 mmol) was added to a round bottom flask, blocked from light, and stirred for 2 hours. After lowering the temperature and extracting the material using dichloromethane (DCM) and water, MgSO 4 and acidic clay were added and stirred. After passing through silica gel, the solvent was removed. Compound BD-8 (1.38 g, yield: 42%) was isolated through column chromatography (Dichloromethane/Hexane).
MS (LC-MS) : 1426.53 m/z [M+]MS (LC-MS): 1426.53 m/z [M + ]
실험예Experiment example 1: 용해도 실험 1: Solubility experiment
상기 제조예에서 제조한 BD105, BD106, BD1, BD8, 하기 화합물 A 및 B를 각각 상온(25℃)에서 톨루엔에 용해시켜 용해도를 측정하였고, 그 결과를 표 1에 나타내었다.BD105, BD106, BD1, BD8, and the following compounds A and B prepared in the above Preparation Example were each dissolved in toluene at room temperature (25°C) to measure solubility, and the results are shown in Table 1.
[화합물 A] [화합물 B][Compound A] [Compound B]
상기 표 1에 나타난 바와 같이, 본 발명의 상기 화학식 1로 표시되는 화합물은, 트리메틸실릴기로 치환된 아미노기를 갖는 비교예 화합물 A 및 디메틸페닐실릴기로 치환된 아미노기를 갖는 비교예 화합물 B에 비하여 톨루엔에 대한 용해도가 현저히 높음을 알 수 있다.As shown in Table 1, the compound represented by Formula 1 of the present invention is more effective in toluene than Comparative Example Compound A, which has an amino group substituted with a trimethylsilyl group, and Comparative Example Compound B, which has an amino group substituted with a dimethylphenylsilyl group. It can be seen that the solubility is significantly high.
실시예Example 1: 유기 발광 소자의 제조 1: Manufacturing of organic light emitting device
ITO (indium tin oxide)가 1,500Å의 두께로 박막 증착된 유리 기판을, 세제를 녹인 증류수에 넣고, 초음파로 세척하였다. ITO를 30분간 세척하였다. 이후, 증류수로 2회 반복하여 초음파 세척을 10분간 진행하였다. 증류수 세척이 끝난 후, 이소프로필알콜 및 아세톤의 용제로 초음파 세척을 각각 30분씩 하고 건조시킨 후, 상기 기판을 글러브박스로 수송시켰다. A glass substrate on which ITO (indium tin oxide) was deposited as a thin film to a thickness of 1,500 Å was placed in distilled water with a detergent dissolved in it and washed with ultrasonic waves. ITO was washed for 30 minutes. Afterwards, ultrasonic cleaning was repeated twice with distilled water for 10 minutes. After washing with distilled water, the substrate was ultrasonic cleaned with isopropyl alcohol and acetone for 30 minutes each, dried, and then transported to a glove box.
이렇게 준비된 ITO 투명 전극 위에 하기 화합물 HIL-1 및 하기 p-dopant로 화합물 IB를 8:2의 중량비로 시클로헥사논에 혼합한 코팅 조성물을 300Å 두께로 스핀 코팅하고, 질소 분위기 하에 핫플레이트에서 220℃ 및 30분 조건으로 코팅 조성물을 경화시켜, 정공 주입층을 형성하였다. 상기 정공 주입층 상에, 하기 화합물 HIL-1을 유기용매(톨루엔: Toluene)에 1%의 중량비로 녹인 조성물을 400Å 두께로 스핀 코팅하고, 질소 분위기 하에 핫플레이트에서 230℃ 및 30분 조건으로 코팅 조성물을 경화시켜, 정공 수송층을 형성하였다. On the ITO transparent electrode prepared in this way, a coating composition obtained by mixing the following compound HIL-1 and the following p-dopant with compound IB in cyclohexanone at a weight ratio of 8:2 was spin-coated to a thickness of 300 Å, and heated at 220°C on a hot plate under a nitrogen atmosphere. And the coating composition was cured for 30 minutes to form a hole injection layer. On the hole injection layer, a composition containing the following compound HIL-1 dissolved in an organic solvent (toluene) at a weight ratio of 1% was spin-coated to a thickness of 400 Å, and coated at 230°C for 30 minutes on a hot plate under a nitrogen atmosphere. The composition was cured to form a hole transport layer.
이 후, 상기 정공 수송층 상에, 하기 호스트 화합물 BH와 상기 제조예 1에서 제조한 도펀트 화합물 BD105(6wt% 농도)를 유기용매(톨루엔: Toluene)에 0.6%의 중량비로 녹인 조성물을 200Å 두께로 스핀 코팅하고, 질소 분위기 하에 핫플레이트에서 120℃ 및 10분 조건으로 코팅 조성물을 경화시켜, 발광층을 형성하였다. Afterwards, on the hole transport layer, a composition containing the following host compound BH and the dopant compound BD105 (6 wt% concentration) prepared in Preparation Example 1 dissolved in an organic solvent (Toluene) at a weight ratio of 0.6% was spun to a thickness of 200 Å. The coating composition was coated and cured at 120° C. for 10 minutes on a hot plate under a nitrogen atmosphere to form a light-emitting layer.
이후, 진공증착기로 옮겨 하기 화합물 ETL-1(200 Å), LiF (12 Å) 및 Al(2000 Å)를 순차적으로 증착하여, 전자수송층, 전자주입층 및 음극을 구비한 유기 발광 소자를 제작하였다. Afterwards, it was transferred to a vacuum evaporator and the following compounds ETL-1 (200 Å), LiF (12 Å), and Al (2000 Å) were sequentially deposited to produce an organic light-emitting device equipped with an electron transport layer, an electron injection layer, and a cathode. .
상기의 과정에서 유기물의 증착 속도는 0.4 내지 0.7Å/sec 를 유지하였고, 캐소드의 LiF는 0.3 Å/ sec, 알루미늄은 2 Å/sec의 증착 속도를 유지하였으며, 증착시 진공도는 2 X 10-7 내지 5 X 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 of the cathode was maintained at 0.3 Å/sec, aluminum was maintained at 2 Å/sec, and the vacuum degree during deposition was 2 to 5
상기 실시예에 사용된 화합물은 하기와 같다.The compounds used in the above examples are as follows.
실시예Example 2 내지 4, 2 to 4, 비교예Comparative example 1 및 1 and 비교예Comparative example 2 2
발광층의 도펀트로 화합물 BD105 대신 하기 표 1에 기재된 화합물을 사용한 것을 제외하고는, 실시예 1과 동일한 방법으로 유기 발광 소자를 제조하였다.An organic light-emitting device was manufactured in the same manner as in Example 1, except that the compounds listed in Table 1 below were used as the dopant of the light-emitting layer instead of compound BD105.
실험예Experiment example 2: 유기 발광 소자 특성 평가 2: Evaluation of organic light emitting device characteristics
상기 실시예 1 내지 4, 비교예 1 및 비교예 2에서 제조한 유기 발광 소자에 전류를 인가하였을 때, 구동전압, 전류효율, 발광효율, 양자효율 및 수명(T50)을 측정하였고 그 결과를 하기 표 2에 나타내었다. T50은 휘도가 초기 휘도에서 50%로 감소되는데 소요되는 시간을 의미한다.When current was applied to the organic light-emitting devices manufactured in Examples 1 to 4, Comparative Examples 1 and 2, the driving voltage, current efficiency, luminous efficiency, quantum efficiency and lifespan (T50) were measured, and the results are as follows. It is shown in Table 2. T50 refers to the time it takes for luminance to decrease to 50% from the initial luminance.
(발광층
도펀트)compound
(luminous layer
dopant)
(V
@10mA/cm2)driving voltage
(V
@10mA/cm 2 )
(lm/W
@10mA/cm2)power efficiency
(lm/W
@10mA/cm 2 )
(cd/A
@10mA/cm2)Luminous efficiency
(cd/A
@10mA/cm 2 )
(%
@10mA/cm2)quantum efficiency
(%
@10mA/cm 2 )
(hr)T50
(hr)
상기 표 2에 나타난 바와 같이, 본 발명의 상기 화학식 1로 표시되는 화합물을 발광층의 도펀트로 사용한 유기 발광 소자는, 트리메틸실릴기로 치환된 아미노기를 갖는 비교예 화합물 A 및 디메틸페닐실릴기로 치환된 아미노기를 갖는 비교예 화합물 B를 발광층의 도펀트로 사용한 유기 발광 소자에 비하여, 구동전압, 효율 및 수명 측면에서 모두 우수한 특성을 나타냄을 알 수 있다. As shown in Table 2, the organic light-emitting device using the compound represented by Formula 1 of the present invention as a dopant of the light-emitting layer includes Comparative Example Compound A having an amino group substituted with a trimethylsilyl group and an amino group substituted with a dimethylphenylsilyl group. It can be seen that compared to the organic light-emitting device using Comparative Example Compound B as a dopant of the light-emitting layer, it exhibits excellent characteristics in terms of driving voltage, efficiency, and lifespan.
1: 기판 2: 양극
3: 발광층 4: 음극
5: 정공주입층 6: 정공수송층
7: 발광층 8: 전자수송층
9: 전자주입층1: Substrate 2: Anode
3: light emitting layer 4: cathode
5: hole injection layer 6: hole transport layer
7: light emitting layer 8: electron transport layer
9: Electron injection layer
Claims (10)
[화학식 1]
상기 화학식 1에서,
R1 및 R2는 각각 독립적으로, 치환 또는 비치환된 C1-60 알킬; 또는 치환 또는 비치환된 C6-60 아릴이고,
L1 및 L2는 각각 독립적으로, 치환 또는 비치환된 C6-60 아릴렌이고,
Ar1 내지 Ar6는 각각 독립적으로, 치환 또는 비치환된 C6-60 아릴이다.
Compound represented by Formula 1:
[Formula 1]
In Formula 1,
R 1 and R 2 are each independently substituted or unsubstituted C 1-60 alkyl; Or substituted or unsubstituted C 6-60 aryl,
L 1 and L 2 are each independently substituted or unsubstituted C 6-60 arylene,
Ar 1 to Ar 6 are each independently substituted or unsubstituted C 6-60 aryl.
R1 및 R2는 각각 독립적으로, 메틸, 또는 페닐인,
화합물.
According to paragraph 1,
R 1 and R 2 are each independently methyl or phenyl,
compound.
L1 및 L2는 각각 독립적으로, 비치환되거나, 또는 할로겐 또는 시아노로 치환된 페닐렌; 또는 비치환되거나, 또는 할로겐 또는 시아노로 치환된 비페닐디일이고,
화합물.
According to paragraph 1,
L 1 and L 2 are each independently phenylene that is unsubstituted or substituted with halogen or cyano; Or it is unsubstituted or biphenyldiyl substituted with halogen or cyano,
compound.
L1 및 L2는 각각 독립적으로, 하기로 구성되는 군으로부터 선택되는 어느 하나인,
화합물:
상기에서,
Z1 내지 Z3는 각각 독립적으로, 수소, 플루오로, 또는 시아노이다.
According to paragraph 1,
L 1 and L 2 are each independently selected from the group consisting of:
compound:
In the above,
Z 1 to Z 3 are each independently hydrogen, fluoro, or cyano.
Ar1 내지 Ar6는 각각 독립적으로, 비치환되거나, 또는 C1-4 알킬로 치환된 C6-20 아릴인,
화합물.
According to paragraph 1,
Ar 1 to Ar 6 are each independently unsubstituted or C 6-20 aryl substituted with C 1-4 alkyl,
compound.
Ar1 내지 Ar6는 서로 동일한,
화합물.
According to paragraph 1,
Ar 1 to Ar 6 are the same as each other,
compound.
Ar1 내지 Ar6는 모두 페닐이거나; 또는
Ar1 내지 Ar6는 모두 4-메틸페닐인,
화합물.
According to clause 6,
Ar 1 to Ar 6 are all phenyl; or
Ar 1 to Ar 6 are all 4-methylphenyl,
compound.
상기 화합물은 하기 화학식 1-1 또는 1-2로 표시되는 화합물:
[화학식 1-1]
[화학식 1-2]
상기 화학식 1-1 및 1-2에서,
R1, R2, L1 및 L2는 제1항에서 정의한 바와 같고,
Z는 각각 독립적으로, 수소, 또는 메틸이다.
According to paragraph 1,
The compound is represented by the following formula 1-1 or 1-2:
[Formula 1-1]
[Formula 1-2]
In Formulas 1-1 and 1-2,
R 1 , R 2 , L 1 and L 2 are as defined in clause 1,
Z is each independently hydrogen or methyl.
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,
compound:
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