JP2011525482A - ２，６−ナフチル単位とイソマンニトール単位とを含有する重合性キラル化合物、およびそのキラルドーパントとしての使用 - Google Patents
２，６−ナフチル単位とイソマンニトール単位とを含有する重合性キラル化合物、およびそのキラルドーパントとしての使用 Download PDFInfo
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- JP2011525482A JP2011525482A JP2011513978A JP2011513978A JP2011525482A JP 2011525482 A JP2011525482 A JP 2011525482A JP 2011513978 A JP2011513978 A JP 2011513978A JP 2011513978 A JP2011513978 A JP 2011513978A JP 2011525482 A JP2011525482 A JP 2011525482A
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- 125000004855 decalinyl group Chemical group C1(CCCC2CCCCC12)* 0.000 description 1
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- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical compound C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 description 1
- ZBKFYXZXZJPWNQ-UHFFFAOYSA-N isothiocyanate group Chemical group [N-]=C=S ZBKFYXZXZJPWNQ-UHFFFAOYSA-N 0.000 description 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 description 1
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- 238000002386 leaching Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 230000002535 lyotropic effect Effects 0.000 description 1
- 125000005439 maleimidyl group Chemical group C1(C=CC(N1*)=O)=O 0.000 description 1
- 125000002960 margaryl 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])C([H])([H])C([H])([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
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methyl-cyclopentane Natural products CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 1
- 125000001421 myristyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001196 nonadecyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([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
- 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
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- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- LFSXCDWNBUNEEM-UHFFFAOYSA-N phthalazine Chemical compound C1=NN=CC2=CC=CC=C21 LFSXCDWNBUNEEM-UHFFFAOYSA-N 0.000 description 1
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- 230000010287 polarization Effects 0.000 description 1
- 229920000636 poly(norbornene) polymer Polymers 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
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- 239000002904 solvent Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([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
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- VOVUARRWDCVURC-UHFFFAOYSA-N thiirane Chemical compound C1CS1 VOVUARRWDCVURC-UHFFFAOYSA-N 0.000 description 1
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- 125000002948 undecyl 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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
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- TUUBOHWZSQXCSW-UHFFFAOYSA-N vanillic acid Natural products COC1=CC(O)=CC(C(O)=O)=C1 TUUBOHWZSQXCSW-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- 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
- C09K19/00—Liquid crystal materials
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K19/58—Dopants or charge transfer agents
- C09K19/586—Optically active dopants; chiral dopants
- C09K19/588—Heterocyclic compounds
-
- 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
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K2019/0444—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group
- C09K2019/0448—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group the end chain group being a polymerizable end group, e.g. -Sp-P or acrylate
-
- 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
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
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| EP08158439.3 | 2008-06-17 | ||
| EP08158439 | 2008-06-17 | ||
| PCT/EP2009/056857 WO2009153168A1 (de) | 2008-06-17 | 2009-06-04 | Polymerisierbare chirale verbindungen, enthaltend 2,6-naphthyl- und isomannit-einheiten, und deren verwendung als chirale dotierstoffe |
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| JP2011525482A true JP2011525482A (ja) | 2011-09-22 |
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| US (1) | US8608977B2 (enExample) |
| EP (1) | EP2297165A1 (enExample) |
| JP (1) | JP2011525482A (enExample) |
| CN (1) | CN102066382A (enExample) |
| TW (1) | TW201011035A (enExample) |
| WO (1) | WO2009153168A1 (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014501737A (ja) * | 2010-12-10 | 2014-01-23 | サビック・イノベーティブ・プラスチックス・アイピー・ベスローテン・フェンノートシャップ | ビスフェノールポリマー構造単位およびその製造方法 |
| JP2015520122A (ja) * | 2012-03-30 | 2015-07-16 | オルネクス ベルギウム ソシエテ アノニム | 放射線硬化性（メタ）アクリル化化合物 |
| JP2017523289A (ja) * | 2014-07-28 | 2017-08-17 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ | ホメオトロピック配向を有する液晶媒体 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102656252B (zh) | 2009-12-17 | 2015-01-14 | 巴斯夫欧洲公司 | 液晶混合物 |
| US9222024B2 (en) | 2010-04-20 | 2015-12-29 | Basf Se | Polymerized films with line texture or fingerprint texture |
| US9309438B2 (en) | 2011-04-05 | 2016-04-12 | ALLNEX Belgium SA | Radiation curable compositions |
| KR101867506B1 (ko) * | 2011-05-23 | 2018-06-15 | 한국생산기술연구원 | 디안히드로헥산헥솔 유도체, 이의 제조방법 및 이를 이용하여 제조된 폴리카보네이트 |
| EP2644634A1 (en) | 2012-03-30 | 2013-10-02 | Cytec Surface Specialties, S.A. | Radiation curable (meth)acrylated compounds |
| EP2818531B1 (en) * | 2013-06-25 | 2017-07-26 | Merck Patent GmbH | Polymerisable compounds and the use thereof in liquid-crystal displays |
| EP3730590A1 (de) * | 2014-03-10 | 2020-10-28 | Merck Patent GmbH | Flüssigkristalline medien mit homöotroper ausrichtung |
| EP3287462A1 (en) * | 2016-08-25 | 2018-02-28 | Nitto Denko Corporation | Isosorbide derivatives to treat bacterial biofilms |
| KR102480330B1 (ko) * | 2017-12-27 | 2022-12-21 | 엘지디스플레이 주식회사 | 유기발광표시장치 |
| CN109825308B (zh) * | 2019-03-19 | 2021-02-02 | 石家庄晶奥量新材料有限公司 | 负性液晶化合物和负性液晶组合物及应用 |
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| JP2000309589A (ja) * | 1999-03-25 | 2000-11-07 | Basf Ag | キラルドーパント、コレステリック液晶組成物、組成物の使用および組成物を含有する化粧および医薬製剤 |
| JP2002155085A (ja) * | 2000-07-13 | 2002-05-28 | Consortium Elektrochem Ind Gmbh | ジアンヒドロヘキシット−ビス−（４−アクリロイルオキシ）アシレートの製造法 |
| JP2002179681A (ja) * | 2000-12-15 | 2002-06-26 | Fuji Photo Film Co Ltd | 光学活性化合物、光反応型キラル剤、液晶組成物、液晶カラーフィルタ、光学フィルム及び記録媒体、並びに液晶の螺旋構造を変化させる方法、液晶の螺旋構造を固定化する方法 |
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| WO2006120220A1 (de) * | 2005-05-11 | 2006-11-16 | Basf Aktiengesellschaft | 2,6-naphthylreste enthaltende verbindungen |
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| JP2014501737A (ja) * | 2010-12-10 | 2014-01-23 | サビック・イノベーティブ・プラスチックス・アイピー・ベスローテン・フェンノートシャップ | ビスフェノールポリマー構造単位およびその製造方法 |
| JP2015520122A (ja) * | 2012-03-30 | 2015-07-16 | オルネクス ベルギウム ソシエテ アノニム | 放射線硬化性（メタ）アクリル化化合物 |
| JP2017523289A (ja) * | 2014-07-28 | 2017-08-17 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ | ホメオトロピック配向を有する液晶媒体 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20110092718A1 (en) | 2011-04-21 |
| US8608977B2 (en) | 2013-12-17 |
| CN102066382A (zh) | 2011-05-18 |
| WO2009153168A1 (de) | 2009-12-23 |
| TW201011035A (en) | 2010-03-16 |
| EP2297165A1 (de) | 2011-03-23 |
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