JP2011513555A5 - - Google Patents
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- Publication number
- JP2011513555A5 JP2011513555A5 JP2010549879A JP2010549879A JP2011513555A5 JP 2011513555 A5 JP2011513555 A5 JP 2011513555A5 JP 2010549879 A JP2010549879 A JP 2010549879A JP 2010549879 A JP2010549879 A JP 2010549879A JP 2011513555 A5 JP2011513555 A5 JP 2011513555A5
- Authority
- JP
- Japan
- Prior art keywords
- ethoxy
- independently
- linker
- liquid crystal
- integer ranging
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 claims description 5
- 230000002535 lyotropic effect Effects 0.000 claims description 3
- 239000004976 Lyotropic liquid crystal Substances 0.000 claims 3
- 230000002378 acidificating effect Effects 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 229910000071 diazene Inorganic materials 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- FVDOBFPYBSDRKH-UHFFFAOYSA-N perylene-3,4,9,10-tetracarboxylic acid Chemical compound C=12C3=CC=C(C(O)=O)C2=C(C(O)=O)C=CC=1C1=CC=C(C(O)=O)C2=C1C3=CC=C2C(=O)O FVDOBFPYBSDRKH-UHFFFAOYSA-N 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- GRFNBEZIAWKNCO-UHFFFAOYSA-N 3-pyridinol Chemical compound OC1=CC=CN=C1 GRFNBEZIAWKNCO-UHFFFAOYSA-N 0.000 description 2
- YUPKXUHVEJJBTD-UHFFFAOYSA-N C1=CC2=C3C(=C1)C4=C5C(=C(C=C4)C(=O)O)C(=C(C(=C5C3=CC=C2)C(=O)NCCOCCOCCOCCOC6=CN=CC=C6)C(=O)N)C(=O)O Chemical compound C1=CC2=C3C(=C1)C4=C5C(=C(C=C4)C(=O)O)C(=C(C(=C5C3=CC=C2)C(=O)NCCOCCOCCOCCOC6=CN=CC=C6)C(=O)N)C(=O)O YUPKXUHVEJJBTD-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- JYWKEVKEKOTYEX-UHFFFAOYSA-N 2,6-dibromo-4-chloroiminocyclohexa-2,5-dien-1-one Chemical compound ClN=C1C=C(Br)C(=O)C(Br)=C1 JYWKEVKEKOTYEX-UHFFFAOYSA-N 0.000 description 1
- 239000012359 Methanesulfonyl chloride Substances 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N anhydrous trimethylamine Natural products CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- 238000007431 microscopic evaluation Methods 0.000 description 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- KIZSMODMWVZSNT-UHFFFAOYSA-N perylene-1,2-dicarboxylic acid Chemical compound C1=CC(C2=C(C(C(=O)O)=CC=3C2=C2C=CC=3)C(O)=O)=C3C2=CC=CC3=C1 KIZSMODMWVZSNT-UHFFFAOYSA-N 0.000 description 1
- CLYVDMAATCIVBF-UHFFFAOYSA-N pigment red 224 Chemical compound C=12C3=CC=C(C(OC4=O)=O)C2=C4C=CC=1C1=CC=C2C(=O)OC(=O)C4=CC=C3C1=C42 CLYVDMAATCIVBF-UHFFFAOYSA-N 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000006158 tetracarboxylic acid group Chemical group 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3490608P | 2008-03-07 | 2008-03-07 | |
| US61/034,906 | 2008-03-07 | ||
| PCT/US2009/036163 WO2009114385A1 (en) | 2008-03-07 | 2009-03-05 | Lyotropic chromophoric compounds, liquid crystal systems and optically anisotropic films |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011513555A JP2011513555A (ja) | 2011-04-28 |
| JP2011513555A5 true JP2011513555A5 (enExample) | 2011-06-16 |
| JP5504180B2 JP5504180B2 (ja) | 2014-05-28 |
Family
ID=40674074
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010549879A Expired - Fee Related JP5504180B2 (ja) | 2008-03-07 | 2009-03-05 | リオトロピック色素化合物、液晶系および光学異方性フィルム |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20110013124A1 (enExample) |
| JP (1) | JP5504180B2 (enExample) |
| KR (1) | KR20100132028A (enExample) |
| CN (1) | CN102007198B (enExample) |
| WO (1) | WO2009114385A1 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005089094A2 (en) * | 2003-11-21 | 2005-09-29 | The Board Of Regents Of The University And Community College System Of Nevada | Materials and methods for the preparation of anisotropically-ordered solids |
| JP5518886B2 (ja) * | 2008-11-05 | 2014-06-11 | 韓国生産技術研究院 | リオトロピッククロモニック液晶組成物、リオトロピッククロモニック液晶コーティング膜の製造方法及びそれによって製造されたリオトロピッククロモニック液晶コーティング膜 |
| KR101703874B1 (ko) * | 2009-12-28 | 2017-02-07 | 엘지디스플레이 주식회사 | 액정표시장치 |
| JP2012255959A (ja) * | 2011-06-10 | 2012-12-27 | Nitto Denko Corp | コーティング液、光学異方性フィルム、及び画像表示装置 |
| JP2013113741A (ja) * | 2011-11-29 | 2013-06-10 | Doshisha | 過酸化脂質の測定方法 |
| GB201300937D0 (en) * | 2013-01-18 | 2013-03-06 | Domino Printing Sciences Plc | Inkjet composition |
| WO2015038579A1 (en) * | 2013-09-11 | 2015-03-19 | Equip, Llc | Discrete peg based dyes |
| NL2016338B1 (en) * | 2016-02-29 | 2017-09-11 | Stichting Katholieke Univ | Stable and homogeneous LCLC alignment on polyimide surfaces. |
| WO2022196605A1 (ja) * | 2021-03-17 | 2022-09-22 | 富士フイルム株式会社 | 組成物、光学異方性膜、円偏光板、表示装置、化合物、化合物の製造方法 |
| CN113248433B (zh) * | 2021-04-15 | 2022-09-09 | 中山大学 | 一种超分子化合物纳米载体及其制备方法和应用 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3017185A1 (de) * | 1980-05-05 | 1981-11-19 | Hoechst Ag, 6000 Frankfurt | Perylen-3,4,9,10-tetracarbonsaeuremonoanhydridmonoimide, verfahren zur herstellung solcher verbindungen und ihre verwendung |
| EP0047027A1 (de) * | 1980-08-22 | 1982-03-10 | BBC Aktiengesellschaft Brown, Boveri & Cie. | Flüssigkristallmischung |
| US4378302A (en) * | 1980-12-16 | 1983-03-29 | General Electric Company | Red perylene dichroic dye containing liquid crystal formulations |
| DE3926564A1 (de) * | 1989-08-11 | 1991-02-14 | Hoechst Ag | Neue pigmentzubereitungen auf basis von perylenverbindungen |
| RU2047643C1 (ru) * | 1993-05-21 | 1995-11-10 | Хан Ир Гвон | Материал для поляризующих покрытий |
| DE10039232A1 (de) * | 2000-08-11 | 2002-02-21 | Basf Ag | Flüssigkristalline Perylen-3,4:9,10-tetracarbonsäurediimide |
| JP4544757B2 (ja) * | 2001-02-23 | 2010-09-15 | 三井化学株式会社 | 有機電界発光素子 |
| RU2207603C2 (ru) * | 2001-06-04 | 2003-06-27 | Хан Ир Гвон | Оптическое устройство для получения и/или преобразования поляризованного электромагнитного излучения и оптическое устройство в виде жидкокристаллического дисплея |
| JP4080364B2 (ja) * | 2002-03-29 | 2008-04-23 | 大日本印刷株式会社 | ラジカル発生剤及び感光性樹脂組成物 |
| US7238792B2 (en) * | 2003-03-18 | 2007-07-03 | Washington State University Research Foundation | Foldable polymers as probes |
| US7160485B2 (en) * | 2003-04-25 | 2007-01-09 | Nitto Denko Corporation | Lyotropic liquid crystal systems based on perylenetetracarboxylic acid dibenzimidazole sulfoderivatives, related anisotropic films, and methods for making |
| GB0312067D0 (en) * | 2003-05-24 | 2003-07-02 | Avecia Ltd | Inks |
| CN100457755C (zh) * | 2003-06-25 | 2009-02-04 | 日东电工株式会社 | 磺基衍生物、及包含其的溶致液晶系统和各向异性膜以及它们的制造方法 |
| US7025900B2 (en) * | 2003-06-25 | 2006-04-11 | Nitto Denko Corporation | Perylenetetracarboxylic acid dibenzimidazole sulfoderivatives containing oxo-groups in the perylene core which form part of a para-quinoid system of bonds, lyotropic liquid crystal systems and anisotropic films containing the same, and methods for making the same |
| US7045177B2 (en) * | 2003-11-21 | 2006-05-16 | Nitto Denko Corporation | Sulfoderivatives of acenaphtho[1,2-b]quinoxaline, lyotropic liquid crystal and anisotropic film on their base |
| JP4525280B2 (ja) * | 2004-09-30 | 2010-08-18 | 三菱化学株式会社 | 異方性色素膜用色素、異方性色素膜形成用組成物、異方性色素膜及び偏光素子 |
-
2009
- 2009-03-05 CN CN200980113782.7A patent/CN102007198B/zh not_active Expired - Fee Related
- 2009-03-05 WO PCT/US2009/036163 patent/WO2009114385A1/en not_active Ceased
- 2009-03-05 KR KR1020107022400A patent/KR20100132028A/ko not_active Ceased
- 2009-03-05 JP JP2010549879A patent/JP5504180B2/ja not_active Expired - Fee Related
- 2009-03-05 US US12/921,385 patent/US20110013124A1/en not_active Abandoned
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