RU2013130877A - Нелинейные аценовые производные и их применение в качестве органических полупроводников - Google Patents
Нелинейные аценовые производные и их применение в качестве органических полупроводников Download PDFInfo
- Publication number
- RU2013130877A RU2013130877A RU2013130877/04A RU2013130877A RU2013130877A RU 2013130877 A RU2013130877 A RU 2013130877A RU 2013130877/04 A RU2013130877/04 A RU 2013130877/04A RU 2013130877 A RU2013130877 A RU 2013130877A RU 2013130877 A RU2013130877 A RU 2013130877A
- Authority
- RU
- Russia
- Prior art keywords
- groups
- atoms
- ring
- thiophene
- group
- Prior art date
Links
- 239000004065 semiconductor Substances 0.000 title claims 3
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical class C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 25
- 125000006413 ring segment Chemical group 0.000 claims abstract 15
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 13
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract 10
- 125000003118 aryl group Chemical group 0.000 claims abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 7
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 6
- 229910052731 fluorine Inorganic materials 0.000 claims abstract 6
- 229910052801 chlorine Inorganic materials 0.000 claims abstract 5
- 125000005842 heteroatom Chemical group 0.000 claims abstract 5
- 229910052740 iodine Inorganic materials 0.000 claims abstract 5
- 229920006395 saturated elastomer Polymers 0.000 claims abstract 5
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims abstract 4
- 125000000304 alkynyl group Chemical group 0.000 claims abstract 4
- 229910052794 bromium Inorganic materials 0.000 claims abstract 4
- 125000003342 alkenyl group Chemical group 0.000 claims abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract 3
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims abstract 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract 3
- 125000004104 aryloxy group Chemical group 0.000 claims abstract 3
- 229910052799 carbon Inorganic materials 0.000 claims abstract 3
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims abstract 3
- 125000004001 thioalkyl group Chemical group 0.000 claims abstract 3
- 125000005553 heteroaryloxy group Chemical group 0.000 claims abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 12
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 10
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 10
- 239000000306 component Substances 0.000 claims 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 6
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 5
- 229930192474 thiophene Natural products 0.000 claims 5
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 4
- AIGNCQCMONAWOL-UHFFFAOYSA-N 1,3-benzoselenazole Chemical compound C1=CC=C2[se]C=NC2=C1 AIGNCQCMONAWOL-UHFFFAOYSA-N 0.000 claims 3
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 claims 3
- ODIRBFFBCSTPTO-UHFFFAOYSA-N 1,3-selenazole Chemical compound C1=C[se]C=N1 ODIRBFFBCSTPTO-UHFFFAOYSA-N 0.000 claims 3
- BNRDGHFESOHOBF-UHFFFAOYSA-N 1-benzoselenophene Chemical compound C1=CC=C2[se]C=CC2=C1 BNRDGHFESOHOBF-UHFFFAOYSA-N 0.000 claims 3
- UITASDKJJNYORO-UHFFFAOYSA-N 389-58-2 Chemical compound S1C=CC2=C1C(SC=C1)=C1C2 UITASDKJJNYORO-UHFFFAOYSA-N 0.000 claims 3
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 3
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 3
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 3
- VGWBXRXNERKBSJ-UHFFFAOYSA-N dithieno[2,3-a:2',3'-d]thiophene Chemical compound C1=CSC2=C1SC1=C2SC=C1 VGWBXRXNERKBSJ-UHFFFAOYSA-N 0.000 claims 3
- 239000000463 material Substances 0.000 claims 3
- 125000002950 monocyclic group Chemical group 0.000 claims 3
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims 3
- 125000003367 polycyclic group Chemical group 0.000 claims 3
- MABNMNVCOAICNO-UHFFFAOYSA-N selenophene Chemical compound C=1C=C[se]C=1 MABNMNVCOAICNO-UHFFFAOYSA-N 0.000 claims 3
- HKGJYTRUDODVMH-UHFFFAOYSA-N selenopheno[2,3-b]selenophene Chemical compound C1=C[se]C2=C1C=C[se]2 HKGJYTRUDODVMH-UHFFFAOYSA-N 0.000 claims 3
- IBDVOHQCXNYOBU-UHFFFAOYSA-N selenopheno[2,3-b]thiophene Chemical compound C1=C[se]C2=C1C=CS2 IBDVOHQCXNYOBU-UHFFFAOYSA-N 0.000 claims 3
- QKDYDXJISKWZQE-UHFFFAOYSA-N selenopheno[3,2-b]selenophene Chemical compound [se]1C=CC2=C1C=C[se]2 QKDYDXJISKWZQE-UHFFFAOYSA-N 0.000 claims 3
- FPDOSPSUXAVNKK-UHFFFAOYSA-N selenopheno[3,2-b]thiophene Chemical compound [se]1C=CC2=C1C=CS2 FPDOSPSUXAVNKK-UHFFFAOYSA-N 0.000 claims 3
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims 3
- URMVZUQDPPDABD-UHFFFAOYSA-N thieno[2,3-f][1]benzothiole Chemical compound C1=C2SC=CC2=CC2=C1C=CS2 URMVZUQDPPDABD-UHFFFAOYSA-N 0.000 claims 3
- VJYJJHQEVLEOFL-UHFFFAOYSA-N thieno[3,2-b]thiophene Chemical compound S1C=CC2=C1C=CS2 VJYJJHQEVLEOFL-UHFFFAOYSA-N 0.000 claims 3
- 230000003287 optical effect Effects 0.000 claims 2
- 230000001681 protective effect Effects 0.000 claims 2
- 125000003107 substituted aryl group Chemical group 0.000 claims 2
- 125000001462 1-pyrrolyl group Chemical group [*]N1C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 238000000018 DNA microarray Methods 0.000 claims 1
- 108091028043 Nucleic acid sequence Proteins 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000005605 benzo group Chemical group 0.000 claims 1
- 239000011230 binding agent Substances 0.000 claims 1
- 239000003990 capacitor Substances 0.000 claims 1
- 239000002800 charge carrier Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- -1 conductive circuits Substances 0.000 claims 1
- 125000006165 cyclic alkyl group Chemical group 0.000 claims 1
- 239000007772 electrode material Substances 0.000 claims 1
- 230000005669 field effect Effects 0.000 claims 1
- 239000010408 film Substances 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000005114 heteroarylalkoxy group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 238000002347 injection Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
- 239000012528 membrane Substances 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 239000005518 polymer electrolyte Substances 0.000 claims 1
- 239000002243 precursor Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 125000006850 spacer group Chemical group 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 239000010409 thin film Substances 0.000 claims 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- 0 C*C#CC(C1=C(*)C(*)[C@](C=CC=CC=CC2)C2=C11)=C(C(C=CC=CC=CC=C2)=C2C2=C3CCCCCCCC2)C3=C1C#C*C Chemical compound C*C#CC(C1=C(*)C(*)[C@](C=CC=CC=CC2)C2=C11)=C(C(C=CC=CC=CC=C2)=C2C2=C3CCCCCCCC2)C3=C1C#C*C 0.000 description 2
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
-
- 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
-
- 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
-
- 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
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/623—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing five rings, e.g. 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
- H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
-
- 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
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
- H10K10/40—Organic transistors
- H10K10/46—Field-effect transistors, e.g. organic thin-film transistors [OTFT]
- H10K10/462—Insulated gate field-effect transistors [IGFETs]
- H10K10/484—Insulated gate field-effect transistors [IGFETs] characterised by the channel regions
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Thin Film Transistor (AREA)
- Electroluminescent Light Sources (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10015339.4 | 2010-12-06 | ||
| EP10015339 | 2010-12-06 | ||
| PCT/EP2011/005621 WO2012076092A1 (en) | 2010-12-06 | 2011-11-09 | Non-linear acene derivatives and their use as organic semiconductors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2013130877A true RU2013130877A (ru) | 2015-01-20 |
Family
ID=44925492
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2013130877/04A RU2013130877A (ru) | 2010-12-06 | 2011-11-09 | Нелинейные аценовые производные и их применение в качестве органических полупроводников |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20130248771A1 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2649082B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2014504284A (cg-RX-API-DMAC7.html) |
| KR (1) | KR20130124347A (cg-RX-API-DMAC7.html) |
| CN (1) | CN103249739B (cg-RX-API-DMAC7.html) |
| RU (1) | RU2013130877A (cg-RX-API-DMAC7.html) |
| SG (1) | SG190738A1 (cg-RX-API-DMAC7.html) |
| TW (1) | TWI516496B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2012076092A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101627494B1 (ko) | 2013-12-10 | 2016-06-13 | 한국화학연구원 | 신규한 전도성 고분자, 이의 제조방법 및 이를 포함하는 유기 전자 소자 |
| KR101678415B1 (ko) | 2013-12-13 | 2016-11-22 | 한국화학연구원 | 신규한 유기 반도체 화합물, 이의 제조방법 및 이를 포함하는 유기 전자 소자 |
| CN106103436B (zh) * | 2014-03-17 | 2019-07-09 | 默克专利股份有限公司 | 有机半导体化合物 |
| US9444060B2 (en) | 2014-04-29 | 2016-09-13 | Sabic Global Technologies B.V. | Synthesis of new small molecules/oligomers with high conductivity and absorption for optoelectronic application |
| WO2016000804A1 (en) * | 2014-06-30 | 2016-01-07 | Merck Patent Gmbh | Extended non-linear acene derivatives and their use as organic semiconductors |
| EP3032599A1 (en) | 2014-12-12 | 2016-06-15 | Solvay SA | Organic semiconductor composition |
| WO2017022761A1 (ja) | 2015-08-04 | 2017-02-09 | 富士フイルム株式会社 | 有機薄膜トランジスタ及びその製造方法、有機薄膜トランジスタ用材料、有機薄膜トランジスタ用組成物、化合物、並びに、有機半導体膜 |
| GB2542346A (en) * | 2015-09-14 | 2017-03-22 | Cambridge Display Tech Ltd | Anthrathiophene derivatives with transverse solubilising units and their applications as organic semiconductors |
| CN110073507B (zh) * | 2017-03-21 | 2023-07-04 | 日本化药株式会社 | 有机半导体组合物、有机薄膜及有机薄膜晶体管 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5892244A (en) | 1989-01-10 | 1999-04-06 | Mitsubishi Denki Kabushiki Kaisha | Field effect transistor including πconjugate polymer and liquid crystal display including the field effect transistor |
| US5198153A (en) | 1989-05-26 | 1993-03-30 | International Business Machines Corporation | Electrically conductive polymeric |
| JP3224829B2 (ja) | 1991-08-15 | 2001-11-05 | 株式会社東芝 | 有機電界効果型素子 |
| WO1996021659A1 (en) | 1995-01-10 | 1996-07-18 | University Of Technology, Sydney | Organic semiconductor |
| EP0889350A1 (en) | 1997-07-03 | 1999-01-07 | ETHZ Institut für Polymere | Photoluminescent display devices (I) |
| US5998804A (en) | 1997-07-03 | 1999-12-07 | Hna Holdings, Inc. | Transistors incorporating substrates comprising liquid crystal polymers |
| GB9726810D0 (en) | 1997-12-19 | 1998-02-18 | Zeneca Ltd | Compounds composition & use |
| WO2000079617A1 (en) | 1999-06-21 | 2000-12-28 | Cambridge University Technical Services Limited | Aligned polymers for an organic tft |
| GB0028867D0 (en) | 2000-11-28 | 2001-01-10 | Avecia Ltd | Field effect translators,methods for the manufacture thereof and materials therefor |
| US20030021913A1 (en) | 2001-07-03 | 2003-01-30 | O'neill Mary | Liquid crystal alignment layer |
| WO2003007396A2 (en) | 2001-07-09 | 2003-01-23 | Plastic Logic Limited | Lamellar polymer architecture |
| EP1783781A3 (en) | 2003-11-28 | 2007-10-03 | Merck Patent GmbH | Organic semiconducting layer formulations comprising polyacenes and organic binder polymers |
| US7495251B2 (en) * | 2006-04-21 | 2009-02-24 | 3M Innovative Properties Company | Electronic devices containing acene-thiophene copolymers with silylethynyl groups |
| EP2132213B1 (en) * | 2007-03-07 | 2013-05-15 | University of Kentucky Research Foundation | Silylethynylated heteroacenes and electronic devices made therewith |
| US8318048B2 (en) * | 2007-04-19 | 2012-11-27 | Merck Patent Gmbh | Process for preparing substituted pentacenes |
| CN101668763A (zh) * | 2007-04-28 | 2010-03-10 | 默克专利股份有限公司 | 有机半导体 |
| KR20110102904A (ko) * | 2008-12-18 | 2011-09-19 | 메르크 파텐트 게엠베하 | 안트라〔２,３-ｂ〕벤조〔ｄ〕티오펜 유도체 및 유기 반도체로서의 이의 용도 |
| US20120048377A1 (en) | 2009-03-05 | 2012-03-01 | Commonwealth Scientific And Industrial Research Organisation | Photosensitive optoelectronic devices comprising polycyclic aromatic compounds |
| US8617720B2 (en) * | 2009-12-21 | 2013-12-31 | E I Du Pont De Nemours And Company | Electroactive composition and electronic device made with the composition |
| CN103124711A (zh) * | 2010-08-11 | 2013-05-29 | E·I·内穆尔杜邦公司 | 电活性化合物和组合物以及用该组合物制成的电子装置 |
-
2011
- 2011-11-09 KR KR1020137017551A patent/KR20130124347A/ko not_active Withdrawn
- 2011-11-09 CN CN201180058820.0A patent/CN103249739B/zh not_active Expired - Fee Related
- 2011-11-09 RU RU2013130877/04A patent/RU2013130877A/ru not_active Application Discontinuation
- 2011-11-09 JP JP2013542386A patent/JP2014504284A/ja active Pending
- 2011-11-09 WO PCT/EP2011/005621 patent/WO2012076092A1/en not_active Ceased
- 2011-11-09 US US13/990,802 patent/US20130248771A1/en not_active Abandoned
- 2011-11-09 SG SG2013042056A patent/SG190738A1/en unknown
- 2011-11-09 EP EP11781453.3A patent/EP2649082B1/en active Active
- 2011-12-05 TW TW100144675A patent/TWI516496B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP2649082B1 (en) | 2015-01-14 |
| CN103249739B (zh) | 2016-02-17 |
| EP2649082A1 (en) | 2013-10-16 |
| TWI516496B (zh) | 2016-01-11 |
| SG190738A1 (en) | 2013-07-31 |
| CN103249739A (zh) | 2013-08-14 |
| JP2014504284A (ja) | 2014-02-20 |
| US20130248771A1 (en) | 2013-09-26 |
| TW201229056A (en) | 2012-07-16 |
| WO2012076092A1 (en) | 2012-06-14 |
| KR20130124347A (ko) | 2013-11-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2013130877A (ru) | Нелинейные аценовые производные и их применение в качестве органических полупроводников | |
| Usta et al. | n-Channel semiconductor materials design for organic complementary circuits | |
| Pappenfus et al. | A π-stacking terthiophene-based quinodimethane is an n-channel conductor in a thin film transistor | |
| Takahashi et al. | Extensive quinoidal oligothiophenes with dicyanomethylene groups at terminal positions as highly amphoteric redox molecules | |
| Fukazawa et al. | Bis-phosphoryl-bridged stilbenes synthesized by an intramolecular cascade cyclization | |
| Cheng et al. | High-performance electrofluorochromic devices based on aromatic polyamides with AIE-active tetraphenylethene and electro-active triphenylamine moieties | |
| RU2013132826A (ru) | Сопряженные полимеры | |
| RU2013110785A (ru) | ПРОИЗВОДНЫЕ АНТРА[2,3-b:7,6-b']ДИТИОФЕНА И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ОРГАНИЧЕСКИХ ПОЛУПРОВОДНИКОВ | |
| CN110506042A (zh) | 有机发光装置以及用于有机发光装置中的有机材料层的组成物 | |
| JP2012528100A5 (cg-RX-API-DMAC7.html) | ||
| RU2012139316A (ru) | Полупроводниковые полимеры | |
| CN109791984B (zh) | 摄像元件用光电转换元件用材料及含有该材料的光电转换元件 | |
| RU2011115113A (ru) | Полимеры, производные бис(тиеноциклопента)бензотиадиазола, и их применение в качестве органических полупроводников | |
| Du et al. | Anthra [2, 3-b] benzo [d] thiophene: an air-stable asymmetric organic semiconductor with high mobility at room temperature | |
| JP2015518497A5 (cg-RX-API-DMAC7.html) | ||
| RU2011115110A (ru) | Полимеры, производные бензобис(силолотиофена), и их применение в качестве органических полупроводниковых | |
| RU2014105870A (ru) | Органические полупроводники | |
| JP2011501451A5 (cg-RX-API-DMAC7.html) | ||
| JP2010502570A (ja) | 置換ベンゾジチオフェン類及びベンゾジセレノフェン類 | |
| JP2017519771A5 (cg-RX-API-DMAC7.html) | ||
| RU2012145007A (ru) | Полимеры 8, 9-дигидробензо[def]карбазола и их применение в качестве органических полупроводников | |
| RU2014147079A (ru) | Блочные структуры для органических электронных устройств | |
| RU2013114919A (ru) | Сопряженные полимеры | |
| CN104685649A (zh) | 有机半导体配制剂 | |
| JP6061888B2 (ja) | 有機薄膜トランジスタ、有機半導体薄膜および有機半導体材料 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA93 | Acknowledgement of application withdrawn (no request for examination) |
Effective date: 20141110 |