KR20010071788A - 실롤 유도체 및 이를 사용한 유기 전계 발광소자 - Google Patents
실롤 유도체 및 이를 사용한 유기 전계 발광소자 Download PDFInfo
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- KR20010071788A KR20010071788A KR1020017000283A KR20017000283A KR20010071788A KR 20010071788 A KR20010071788 A KR 20010071788A KR 1020017000283 A KR1020017000283 A KR 1020017000283A KR 20017000283 A KR20017000283 A KR 20017000283A KR 20010071788 A KR20010071788 A KR 20010071788A
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- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 125000002971 oxazolyl group Chemical group 0.000 description 2
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- 125000003367 polycyclic group Chemical group 0.000 description 1
- 239000007774 positive electrode material Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 125000001567 quinoxalinyl group Chemical class N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 230000027756 respiratory electron transport chain Effects 0.000 description 1
- YYMBJDOZVAITBP-UHFFFAOYSA-N rubrene Chemical compound C1=CC=CC=C1C(C1=C(C=2C=CC=CC=2)C2=CC=CC=C2C(C=2C=CC=CC=2)=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 YYMBJDOZVAITBP-UHFFFAOYSA-N 0.000 description 1
- UTUZBCDXWYMYGA-UHFFFAOYSA-N silafluorene Chemical compound C12=CC=CC=C2CC2=C1C=CC=[Si]2 UTUZBCDXWYMYGA-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 150000003413 spiro compounds Chemical class 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- 125000005425 toluyl group Chemical group 0.000 description 1
- JFLKFZNIIQFQBS-FNCQTZNRSA-N trans,trans-1,4-Diphenyl-1,3-butadiene Chemical compound C=1C=CC=CC=1\C=C\C=C\C1=CC=CC=C1 JFLKFZNIIQFQBS-FNCQTZNRSA-N 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical group [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
- 125000005259 triarylamine group Chemical group 0.000 description 1
- SROUVPKSYJDACC-UHFFFAOYSA-N trimethyl-[3-[2-(3-trimethylsilylphenyl)ethynyl]phenyl]silane Chemical group C[Si](C)(C)C1=CC=CC(C#CC=2C=C(C=CC=2)[Si](C)(C)C)=C1 SROUVPKSYJDACC-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
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000001018 xanthene dye Substances 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
-
- 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
- C07F7/0805—Compounds with Si-C or Si-Si linkages comprising only Si, C or H atoms
- C07F7/0807—Compounds with Si-C or Si-Si linkages comprising only Si, C or H atoms comprising Si as a ring atom
-
- 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
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
- C07F7/0816—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring comprising Si as a ring atom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- 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
-
- 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
- H10K85/40—Organosilicon compounds, e.g. TIPS pentacene
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
Description
Claims (5)
- 하기 화학식 1의 실롤 유도체.화학식 1상기 식에서,R1과 R2는 각각 독립적으로 치환되거나 치환되지 않은 알킬기, 실릴기, 아릴기, 헤테로사이클릭기 또는 알케닐기이며, 각각의 말단에서 서로 결합할 수 있으며,Ar1과 Ar2는 각각 독립적으로 치환되거나 치환되지 않은 아릴기 또는 헤테로사이클릭기이며,R3내지 R10은 각각 독립적으로 치환되거나 치환되지 않은 알킬기, 아릴기 또는 헤테로사이클릭기이며, 각각의 말단에서 서로 결합할 수 있다.
- 하기 화학식 2의 실롤 유도체.화학식 2상기 식에서,R11내지 R30은 각각 독립적으로 치환되거나 치환되지 않은 알킬기, 아릴기 또는 헤테로사이클릭기이며, 각각의 말단에서 서로 결합할 수 있으며,R3내지 R10은 각각 독립적으로 치환되거나 치환되지 않은 알킬기, 아릴기 또는 헤테로사이클릭기이며, 각각의 말단에서 서로 결합할 수 있다.
- 하기 화학식 3의 실롤 유도체.화학식 3상기 식에서,A1및 A2는 서로 결합하여 5원 환 또는 6원 환을 형성하고,B1및 B2는 서로 결합하여 5원 환 또는 6원 환을 형성하고,C1및 C2는 서로 결합하여 5원 환 또는 6원 환을 형성하고,D1및 D2는 서로 결합하여 5원 환 또는 6원 환을 형성한다.
- 하기 화학식 4의 실롤 유도체.화학식 4상기 식에서,A1및 A2는 서로 결합하여 5원 환 또는 6원 환을 형성하고,B1및 B2는 서로 결합하여 5원 환 또는 6원 환을 형성하고,C1및 C2는 서로 결합하여 5원 환 또는 6원 환을 형성하고,E1및 E2는 서로 결합하여 5원 환 또는 6원 환을 형성하고,X는 산소, 황 또는 NR(여기서, R은 수소, 알킬기 또는 아릴기이다)이다.
- 제1항 내지 제4항 중의 어느 한 항에 따른 실롤 유도체를 발광층에 사용한 유기 전계 발광소자.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP98-210388 | 1998-07-09 | ||
JP21038898 | 1998-07-09 |
Publications (2)
Publication Number | Publication Date |
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KR20010071788A true KR20010071788A (ko) | 2001-07-31 |
KR100625505B1 KR100625505B1 (ko) | 2006-09-20 |
Family
ID=16588518
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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KR1020017000283A KR100625505B1 (ko) | 1998-07-09 | 1999-07-07 | 실롤 유도체 및 이를 사용한 유기 전계 발광소자 |
Country Status (5)
Country | Link |
---|---|
US (1) | US6376694B1 (ko) |
EP (1) | EP1113017B1 (ko) |
KR (1) | KR100625505B1 (ko) |
DE (1) | DE69929067D1 (ko) |
WO (1) | WO2000002886A1 (ko) |
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KR20030043264A (ko) * | 2001-11-27 | 2003-06-02 | 박철홍 | 전자결핍성화합물과 특이반응하는 폴리치환된 실롤-저몰나노와이어 및 그 제조방법 |
KR100711733B1 (ko) * | 2005-10-26 | 2007-04-25 | 주식회사 두산 | 실롤 덴드리머, 이를 포함하는 전계 발광 소자, 및 그제조방법 |
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-
1999
- 1999-07-07 KR KR1020017000283A patent/KR100625505B1/ko not_active IP Right Cessation
- 1999-07-07 US US09/743,426 patent/US6376694B1/en not_active Expired - Fee Related
- 1999-07-07 EP EP99929736A patent/EP1113017B1/en not_active Expired - Lifetime
- 1999-07-07 WO PCT/JP1999/003671 patent/WO2000002886A1/ja active IP Right Grant
- 1999-07-07 DE DE69929067T patent/DE69929067D1/de not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20030043264A (ko) * | 2001-11-27 | 2003-06-02 | 박철홍 | 전자결핍성화합물과 특이반응하는 폴리치환된 실롤-저몰나노와이어 및 그 제조방법 |
KR100711733B1 (ko) * | 2005-10-26 | 2007-04-25 | 주식회사 두산 | 실롤 덴드리머, 이를 포함하는 전계 발광 소자, 및 그제조방법 |
Also Published As
Publication number | Publication date |
---|---|
KR100625505B1 (ko) | 2006-09-20 |
US6376694B1 (en) | 2002-04-23 |
EP1113017B1 (en) | 2005-12-21 |
EP1113017A4 (en) | 2003-07-23 |
EP1113017A1 (en) | 2001-07-04 |
DE69929067D1 (de) | 2006-01-26 |
WO2000002886A1 (fr) | 2000-01-20 |
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