JP6072760B2 - エレクトロニクス用途のための4H−イミダゾ[1,2−a]イミダゾール - Google Patents
エレクトロニクス用途のための4H−イミダゾ[1,2−a]イミダゾール Download PDFInfo
- Publication number
- JP6072760B2 JP6072760B2 JP2014501544A JP2014501544A JP6072760B2 JP 6072760 B2 JP6072760 B2 JP 6072760B2 JP 2014501544 A JP2014501544 A JP 2014501544A JP 2014501544 A JP2014501544 A JP 2014501544A JP 6072760 B2 JP6072760 B2 JP 6072760B2
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- aryl
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- 0 CCCC*c1c(*)[n](C(CC)(CC)I)c2*(*)c(*)n[n]12 Chemical compound CCCC*c1c(*)[n](C(CC)(CC)I)c2*(*)c(*)n[n]12 0.000 description 27
- UWDTYENJIOEORT-UHFFFAOYSA-N C[n]1c2nc(cccc3)c3[n]2c2ccccc12 Chemical compound C[n]1c2nc(cccc3)c3[n]2c2ccccc12 UWDTYENJIOEORT-UHFFFAOYSA-N 0.000 description 3
- IPAIJAHZKASIRX-UHFFFAOYSA-N Cc1ccc2[n](C)c3ccccc3c2c1 Chemical compound Cc1ccc2[n](C)c3ccccc3c2c1 IPAIJAHZKASIRX-UHFFFAOYSA-N 0.000 description 2
- TVVXNMSFBQPOSU-UHFFFAOYSA-N Cc1ccc2[o]c(c(C)ccc3)c3c2c1 Chemical compound Cc1ccc2[o]c(c(C)ccc3)c3c2c1 TVVXNMSFBQPOSU-UHFFFAOYSA-N 0.000 description 2
- UQWZLNDZKILIMK-UHFFFAOYSA-N Cc1ccc2[o]c3ccc(C)cc3c2c1 Chemical compound Cc1ccc2[o]c3ccc(C)cc3c2c1 UQWZLNDZKILIMK-UHFFFAOYSA-N 0.000 description 2
- PVBRAGJTHQZENQ-UHFFFAOYSA-N Cc1cccc2c1[o]c1c2cccc1C Chemical compound Cc1cccc2c1[o]c1c2cccc1C PVBRAGJTHQZENQ-UHFFFAOYSA-N 0.000 description 2
- KLACMEYLRXQSMN-UHFFFAOYSA-N c(cc1)cc([nH]2)c1[n]1c2nc2ccccc12 Chemical compound c(cc1)cc([nH]2)c1[n]1c2nc2ccccc12 KLACMEYLRXQSMN-UHFFFAOYSA-N 0.000 description 2
- XGEJVLWJGJUSFU-UHFFFAOYSA-N Brc(cc1c2c3)ccc1[o]c2ccc3-[n]1c2nc(cccc3)c3[n]2c2c1cccc2 Chemical compound Brc(cc1c2c3)ccc1[o]c2ccc3-[n]1c2nc(cccc3)c3[n]2c2c1cccc2 XGEJVLWJGJUSFU-UHFFFAOYSA-N 0.000 description 1
- BWOSCTZLKMWUBX-UHFFFAOYSA-N Brc1cc(-[n]2c3ncc[n]3c3c2cccc3)ccc1 Chemical compound Brc1cc(-[n]2c3ncc[n]3c3c2cccc3)ccc1 BWOSCTZLKMWUBX-UHFFFAOYSA-N 0.000 description 1
- UZYPRIYRAAIWNB-UHFFFAOYSA-N Brc1cc(N2C3=NC4C=CC=CC4N3C=C2)ccc1 Chemical compound Brc1cc(N2C3=NC4C=CC=CC4N3C=C2)ccc1 UZYPRIYRAAIWNB-UHFFFAOYSA-N 0.000 description 1
- GEJOQRIYFDKSDH-UHFFFAOYSA-N Brc1cccc(-[n](c(cccc2)c2c2c3)c2ccc3-[n]2c3nc4ccccc4[n]3c3c2cccc3)c1 Chemical compound Brc1cccc(-[n](c(cccc2)c2c2c3)c2ccc3-[n]2c3nc4ccccc4[n]3c3c2cccc3)c1 GEJOQRIYFDKSDH-UHFFFAOYSA-N 0.000 description 1
- DUZULECEDQWISJ-UHFFFAOYSA-N Brc1cccc(c2c3)c1[o]c2ccc3-[n]1c2nc3ccccc3[n]2c2ccccc12 Chemical compound Brc1cccc(c2c3)c1[o]c2ccc3-[n]1c2nc3ccccc3[n]2c2ccccc12 DUZULECEDQWISJ-UHFFFAOYSA-N 0.000 description 1
- RPXXZYWDKGCJJY-UHFFFAOYSA-N C(C1)C=Cc([n]2-c3cc(-c(cc4c5c6)ccc4[o]c5ccc6-[n]4c5nc(cccc6)c6[n]5c5c4cccc5)ccc3)c1[n]1c2nc2c1cccc2 Chemical compound C(C1)C=Cc([n]2-c3cc(-c(cc4c5c6)ccc4[o]c5ccc6-[n]4c5nc(cccc6)c6[n]5c5c4cccc5)ccc3)c1[n]1c2nc2c1cccc2 RPXXZYWDKGCJJY-UHFFFAOYSA-N 0.000 description 1
- DHZVDTUSHFSGAM-UHFFFAOYSA-N C1N=C(N(c2c3cccc2)c(cc2)cc(c4c5)c2[o]c4ccc5-[n]2c4ncn[n]4c4ccccc24)N3N1 Chemical compound C1N=C(N(c2c3cccc2)c(cc2)cc(c4c5)c2[o]c4ccc5-[n]2c4ncn[n]4c4ccccc24)N3N1 DHZVDTUSHFSGAM-UHFFFAOYSA-N 0.000 description 1
- KSWNAFGWXTYILB-UHFFFAOYSA-N CC(C)(C12)C(C)(C=C)C(C=CCC3)=C3N1c1ncncc1N2c1ccccc1 Chemical compound CC(C)(C12)C(C)(C=C)C(C=CCC3)=C3N1c1ncncc1N2c1ccccc1 KSWNAFGWXTYILB-UHFFFAOYSA-N 0.000 description 1
- ZTAYRGAXOXGHFT-UHFFFAOYSA-N CC(C)(C12)C(C)(C=C)c(cccc3)c3N1c1cncnc1N2c1c(C)cccc1 Chemical compound CC(C)(C12)C(C)(C=C)c(cccc3)c3N1c1cncnc1N2c1c(C)cccc1 ZTAYRGAXOXGHFT-UHFFFAOYSA-N 0.000 description 1
- QREQICNEXFKBQV-UHFFFAOYSA-N CC(C)(C12)C(C)(C=C)c(cccc3)c3N1c1cncnc1N2c1ccncc1 Chemical compound CC(C)(C12)C(C)(C=C)c(cccc3)c3N1c1cncnc1N2c1ccncc1 QREQICNEXFKBQV-UHFFFAOYSA-N 0.000 description 1
- AGMOLWIKNFCLDX-UHFFFAOYSA-N CC(C)(C12)C(C)(C=C)c(cccc3)c3N1c1cncnc1N2c1cnccc1 Chemical compound CC(C)(C12)C(C)(C=C)c(cccc3)c3N1c1cncnc1N2c1cnccc1 AGMOLWIKNFCLDX-UHFFFAOYSA-N 0.000 description 1
- HNQDPHRXWNYMEI-RGURZIINSA-N CC(C)CC1(C2)[I]2N(C)[C@@H](C)C1 Chemical compound CC(C)CC1(C2)[I]2N(C)[C@@H](C)C1 HNQDPHRXWNYMEI-RGURZIINSA-N 0.000 description 1
- FANCSRVJIWXFPB-UHFFFAOYSA-N CC(C)N(C1C(C)(C)C2(C)C)c3ncncc3N1C1=C2C=CCC1 Chemical compound CC(C)N(C1C(C)(C)C2(C)C)c3ncncc3N1C1=C2C=CCC1 FANCSRVJIWXFPB-UHFFFAOYSA-N 0.000 description 1
- NSWCMUKFNFJCFU-UHFFFAOYSA-N CC(C)c1cccc(C(C)C)c1-c(nc12)ncc1N(C)C(C1(C)C3(C)C1)N2C1=C3C=CCC1 Chemical compound CC(C)c1cccc(C(C)C)c1-c(nc12)ncc1N(C)C(C1(C)C3(C)C1)N2C1=C3C=CCC1 NSWCMUKFNFJCFU-UHFFFAOYSA-N 0.000 description 1
- ROLZRRHACVRKQI-UHFFFAOYSA-N CC12Nc3ncn[n]3C1C=CC=C2 Chemical compound CC12Nc3ncn[n]3C1C=CC=C2 ROLZRRHACVRKQI-UHFFFAOYSA-N 0.000 description 1
- YTIQIQPKCFIDPV-UHFFFAOYSA-N CCC/C=[I]\CNC Chemical compound CCC/C=[I]\CNC YTIQIQPKCFIDPV-UHFFFAOYSA-N 0.000 description 1
- VQMFVMOJLQINEV-UHFFFAOYSA-N CCC1(C)C(CC)(C=C)c(cccc2)c2N2c(ncnc3)c3N(C)C12 Chemical compound CCC1(C)C(CC)(C=C)c(cccc2)c2N2c(ncnc3)c3N(C)C12 VQMFVMOJLQINEV-UHFFFAOYSA-N 0.000 description 1
- DTOVPKZQRWXXPT-LBJKSBDHSA-N CCCCC[C@@H](C)C(C)N(C1CCCCC1)[C@](C)(N)N[C@H](C)CCCCC Chemical compound CCCCC[C@@H](C)C(C)N(C1CCCCC1)[C@](C)(N)N[C@H](C)CCCCC DTOVPKZQRWXXPT-LBJKSBDHSA-N 0.000 description 1
- AKEZNXGHDYJLRD-UHFFFAOYSA-N Cc(cc1)cc(c2c3)c1[o]c2ccc3-c1cccc(-c2ccc3[o]c4ccc(C)cc4c3c2)c1 Chemical compound Cc(cc1)cc(c2c3)c1[o]c2ccc3-c1cccc(-c2ccc3[o]c4ccc(C)cc4c3c2)c1 AKEZNXGHDYJLRD-UHFFFAOYSA-N 0.000 description 1
- GOHDQJMHFDTVMX-UHFFFAOYSA-N Cc1cccc(c2c3)c1[o]c2ccc3I Chemical compound Cc1cccc(c2c3)c1[o]c2ccc3I GOHDQJMHFDTVMX-UHFFFAOYSA-N 0.000 description 1
- NOQNQJVAQOCWQY-UHFFFAOYSA-N Ic(cc1I)cc2c1[o]c1ccccc21 Chemical compound Ic(cc1I)cc2c1[o]c1ccccc21 NOQNQJVAQOCWQY-UHFFFAOYSA-N 0.000 description 1
- XVCGYFKSNIPQBK-UHFFFAOYSA-N Ic(cc1c2cc(-[n]3c4nc(cccc5)c5[n]4c4c3cccc4)ccc22)ccc1[n]2-c1ccccc1 Chemical compound Ic(cc1c2cc(-[n]3c4nc(cccc5)c5[n]4c4c3cccc4)ccc22)ccc1[n]2-c1ccccc1 XVCGYFKSNIPQBK-UHFFFAOYSA-N 0.000 description 1
- PDJBQDQTPXEDES-UHFFFAOYSA-N Nc(cccc1)c1Nc1ccccc1Nc(cc1-[n]2c3nc(cccc4)c4[n]3c3ccccc23)cc2c1[o]c1ccccc21 Chemical compound Nc(cccc1)c1Nc1ccccc1Nc(cc1-[n]2c3nc(cccc4)c4[n]3c3ccccc23)cc2c1[o]c1ccccc21 PDJBQDQTPXEDES-UHFFFAOYSA-N 0.000 description 1
- FCYHLWUKNVLXJV-UHFFFAOYSA-N c(cc1)cc(c2ccccc22)c1[n]2-c1ccc2[o]c(ccc(-[n]3c(cccc4)c4c4c3cccc4)c3)c3c2c1 Chemical compound c(cc1)cc(c2ccccc22)c1[n]2-c1ccc2[o]c(ccc(-[n]3c(cccc4)c4c4c3cccc4)c3)c3c2c1 FCYHLWUKNVLXJV-UHFFFAOYSA-N 0.000 description 1
- IXPZYJRRDFZWHJ-UHFFFAOYSA-N c1cnc2[n]1c(cccc1)c1[nH]2 Chemical compound c1cnc2[n]1c(cccc1)c1[nH]2 IXPZYJRRDFZWHJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
- C09B57/008—Triarylamine dyes containing no other chromophores
-
- 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
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
-
- 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
-
- 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
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/14—Carrier transporting layers
- H10K50/15—Hole transporting 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
-
- 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
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
-
- 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
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6574—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K99/00—Subject matter not provided for in other groups of this subclass
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Optics & Photonics (AREA)
- Electromagnetism (AREA)
- Electroluminescent Light Sources (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
- Photovoltaic Devices (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11159805.8 | 2011-03-25 | ||
| EP11159805 | 2011-03-25 | ||
| EP11188571.1 | 2011-11-10 | ||
| EP11188571 | 2011-11-10 | ||
| PCT/EP2012/055064 WO2012130709A1 (en) | 2011-03-25 | 2012-03-22 | 4h-imidazo[1,2-a]imidazoles for electronic applications |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016252932A Division JP6471141B2 (ja) | 2011-03-25 | 2016-12-27 | エレクトロニクス用途のための4H−イミダゾ[1,2−a]イミダゾール |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014515014A JP2014515014A (ja) | 2014-06-26 |
| JP2014515014A5 JP2014515014A5 (enExample) | 2016-05-12 |
| JP6072760B2 true JP6072760B2 (ja) | 2017-02-01 |
Family
ID=45928850
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014501544A Active JP6072760B2 (ja) | 2011-03-25 | 2012-03-22 | エレクトロニクス用途のための4H−イミダゾ[1,2−a]イミダゾール |
| JP2016252932A Active JP6471141B2 (ja) | 2011-03-25 | 2016-12-27 | エレクトロニクス用途のための4H−イミダゾ[1,2−a]イミダゾール |
| JP2019007613A Active JP6730470B2 (ja) | 2011-03-25 | 2019-01-21 | エレクトロニクス用途のための4H−イミダゾ[1,2−a]イミダゾール |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016252932A Active JP6471141B2 (ja) | 2011-03-25 | 2016-12-27 | エレクトロニクス用途のための4H−イミダゾ[1,2−a]イミダゾール |
| JP2019007613A Active JP6730470B2 (ja) | 2011-03-25 | 2019-01-21 | エレクトロニクス用途のための4H−イミダゾ[1,2−a]イミダゾール |
Country Status (5)
| Country | Link |
|---|---|
| EP (3) | EP3640252B1 (enExample) |
| JP (3) | JP6072760B2 (enExample) |
| KR (4) | KR102393687B1 (enExample) |
| CN (3) | CN114315840A (enExample) |
| WO (1) | WO2012130709A1 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2017071641A (ja) * | 2011-03-25 | 2017-04-13 | ユー・ディー・シー アイルランド リミテッド | エレクトロニクス用途のための4H−イミダゾ[1,2−a]イミダゾール |
| US10431750B2 (en) | 2011-03-25 | 2019-10-01 | Udc Ireland Limited | 4H-imidazo[1,2-a]imidazoles for electronic applications |
Families Citing this family (61)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101947206B1 (ko) * | 2011-04-13 | 2019-02-12 | 메르크 파텐트 게엠베하 | 전자 소자용 재료 |
| EP2707456B1 (en) | 2011-05-10 | 2018-09-26 | Basf Se | Novel color converters |
| ES2671232T3 (es) | 2011-06-10 | 2018-06-05 | Basf Se | Nuevo dispositivo de iluminación que comprende un convertidor de color |
| CN108299439B (zh) | 2011-11-10 | 2021-02-09 | Udc 爱尔兰有限责任公司 | 用于电子应用的4H-咪唑并[1,2-a]咪唑 |
| US9620724B2 (en) * | 2012-07-10 | 2017-04-11 | Udc Ireland Limited | Benzimidazo[1,2-A]benzimidazole derivatives for electronic applications |
| KR102127406B1 (ko) | 2012-09-20 | 2020-06-29 | 유디씨 아일랜드 리미티드 | 전자 응용을 위한 아자디벤조푸란 |
| KR102164633B1 (ko) | 2013-03-20 | 2020-10-13 | 유디씨 아일랜드 리미티드 | Oled에서 효율 부스터로서의 아자벤즈이미다졸 카르벤 착체 |
| CN104119364A (zh) * | 2013-04-25 | 2014-10-29 | 海洋王照明科技股份有限公司 | 一种有机半导体材料、制备方法和电致发光器件 |
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| JP2017071641A (ja) * | 2011-03-25 | 2017-04-13 | ユー・ディー・シー アイルランド リミテッド | エレクトロニクス用途のための4H−イミダゾ[1,2−a]イミダゾール |
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| US11450812B2 (en) | 2011-03-25 | 2022-09-20 | Udc Ireland Limited | 4H-imidazo[1,2-a]imidazoles for electronic applications |
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| CN106188065B (zh) | 2021-12-28 |
| KR102266455B1 (ko) | 2021-06-21 |
| JP2014515014A (ja) | 2014-06-26 |
| EP3640252B1 (en) | 2022-03-16 |
| KR102116313B1 (ko) | 2020-06-01 |
| EP2688889B1 (en) | 2016-05-18 |
| WO2012130709A1 (en) | 2012-10-04 |
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