JP2003261511A5 - - Google Patents
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- JP2003261511A5 JP2003261511A5 JP2002381295A JP2002381295A JP2003261511A5 JP 2003261511 A5 JP2003261511 A5 JP 2003261511A5 JP 2002381295 A JP2002381295 A JP 2002381295A JP 2002381295 A JP2002381295 A JP 2002381295A JP 2003261511 A5 JP2003261511 A5 JP 2003261511A5
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- Prior art keywords
- compounds
- carbon atoms
- mol
- formula
- alkyl
- 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.)
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- 150000001875 compounds Chemical class 0.000 description 21
- 125000004432 carbon atom Chemical group C* 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 8
- 239000004973 liquid crystal related substance Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- 229910004013 NO 2 Inorganic materials 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- QLKWZXXUWUOXCH-UHFFFAOYSA-N 2,3-difluorobenzene-1,4-diol Chemical compound OC1=CC=C(O)C(F)=C1F QLKWZXXUWUOXCH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229920006254 polymer film Polymers 0.000 description 3
- 238000010626 work up procedure Methods 0.000 description 3
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 2
- 0 Cc(c(O)c(c(*)c1O)I)c1I Chemical compound Cc(c(O)c(c(*)c1O)I)c1I 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000012788 optical film Substances 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 125000004434 sulfur atom Chemical group 0.000 description 2
- GOYDNIKZWGIXJT-UHFFFAOYSA-N 1,2-difluorobenzene Chemical compound FC1=CC=CC=C1F GOYDNIKZWGIXJT-UHFFFAOYSA-N 0.000 description 1
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- INUNLMUAPJVRME-UHFFFAOYSA-N 3-chloropropanoyl chloride Chemical compound ClCCC(Cl)=O INUNLMUAPJVRME-UHFFFAOYSA-N 0.000 description 1
- JPEVEWTZGBSVHD-UHFFFAOYSA-N 3-ethenoxy-1-(3-ethenoxyprop-1-enoxy)prop-1-ene Chemical compound C(=C)OCC=COC=CCOC=C JPEVEWTZGBSVHD-UHFFFAOYSA-N 0.000 description 1
- 229960000549 4-dimethylaminophenol Drugs 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 102100026827 Protein associated with UVRAG as autophagy enhancer Human genes 0.000 description 1
- 101710102978 Protein associated with UVRAG as autophagy enhancer Proteins 0.000 description 1
- MDMKOESKPAVFJF-UHFFFAOYSA-N [4-(2-methylprop-2-enoyloxy)phenyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=C(OC(=O)C(C)=C)C=C1 MDMKOESKPAVFJF-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 229940039227 diagnostic agent Drugs 0.000 description 1
- 239000000032 diagnostic agent Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 238000005401 electroluminescence Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- AJSTXXYNEIHPMD-UHFFFAOYSA-N triethyl borate Chemical compound CCOB(OCC)OCC AJSTXXYNEIHPMD-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01130617.2 | 2001-12-27 | ||
| EP01130617 | 2001-12-27 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003261511A JP2003261511A (ja) | 2003-09-19 |
| JP2003261511A5 true JP2003261511A5 (https=) | 2006-02-16 |
| JP4553550B2 JP4553550B2 (ja) | 2010-09-29 |
Family
ID=8179644
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002381295A Expired - Fee Related JP4553550B2 (ja) | 2001-12-27 | 2002-12-27 | 重合可能な単環式化合物 |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US7465479B2 (https=) |
| JP (1) | JP4553550B2 (https=) |
| DE (1) | DE10257711B4 (https=) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10308514A1 (de) * | 2003-02-26 | 2004-09-09 | Schott Glas | OLED mit Berührungssensor |
| CN100446079C (zh) * | 2004-12-15 | 2008-12-24 | 日本电气株式会社 | 液晶显示装置、其驱动方法及其驱动电路 |
| US7575696B2 (en) * | 2006-07-28 | 2009-08-18 | Fujifilm Corporation | Liquid crystal composition and anisotropic material |
| TWI354677B (en) * | 2007-01-31 | 2011-12-21 | Au Optronics Corp | Photosensitive monomer, liquid crystal material ha |
| TWI349029B (en) * | 2007-03-30 | 2011-09-21 | Au Optronics Corp | Liquid crystalline medium, liquid crystal display panel using the same, and method for manufacturing liquid crystal display panel |
| TWI336017B (en) * | 2007-10-24 | 2011-01-11 | Au Optronics Corp | Method for manufacturing liquid crystal display |
| TWI395993B (zh) * | 2008-06-30 | 2013-05-11 | Au Optronics Corp | 液晶顯示面板及其液晶材料 |
| EP2352060B1 (en) * | 2008-10-21 | 2013-05-15 | Sharp Kabushiki Kaisha | Orientation film, orientation film material, liquid crystal display having orientation film, and method for forming the same |
| TWI383214B (zh) * | 2008-10-22 | 2013-01-21 | Au Optronics Corp | 液晶顯示器結構 |
| EP2221592A1 (en) * | 2009-01-22 | 2010-08-25 | Stichting Dutch Polymer Institute | Multifunctional optical sensor |
| US8176924B2 (en) * | 2009-03-11 | 2012-05-15 | Kent Displays Incorporated | Color changing artificial fingernails |
| TWI388905B (zh) * | 2009-03-17 | 2013-03-11 | Au Optronics Corp | 液晶顯示面板及其製造方法 |
| US8168084B2 (en) | 2009-12-18 | 2012-05-01 | Vanderbilt University | Polar nematic compounds |
| DE102011009691A1 (de) * | 2010-02-09 | 2011-08-11 | Merck Patent GmbH, 64293 | Flüssigkristallines Medium |
| GB201208115D0 (en) * | 2012-05-09 | 2012-06-20 | Lomox Ltd | Oilgomeric organic light emitting diode (OLED) materrials containing multiple crosslinking functions |
| JP6312375B2 (ja) * | 2012-06-29 | 2018-04-18 | 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 | 液晶媒体 |
| CN104178180B (zh) * | 2014-07-17 | 2016-04-06 | 北京大学 | 一种具有大双折射率的向列相液晶材料及其应用 |
| JP2019501233A (ja) * | 2015-10-30 | 2019-01-17 | メルク・パテント・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ ＧｍｂＨ | 液晶媒体 |
| EP3857301B1 (fr) | 2018-09-27 | 2025-02-19 | Saint-Gobain Glass France | Dispositif electrocommandable a diffusion variable par cristaux liquides et son procede de fabrication |
| FR3086771A1 (fr) | 2018-09-27 | 2020-04-03 | Saint-Gobain Glass France | Dispositif electrocommandable a diffusion variable par cristaux liquides et son procede. |
| FR3108990A1 (fr) | 2020-04-01 | 2021-10-08 | Saint-Gobain Glass France | Dispositif electrocommandable a diffusion variable par cristaux liquides et son procede |
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| GB2357061B (en) | 1999-12-08 | 2003-09-17 | Merck Patent Gmbh | Hot stamping foils |
| TWI236496B (en) * | 2000-03-16 | 2005-07-21 | Merck Patent Gmbh | Broadband liquid crystal pigments |
| AU2001281885A1 (en) | 2000-07-13 | 2002-01-30 | Merck Patent G.M.B.H | Chiral compounds iii |
| WO2002006196A1 (en) | 2000-07-13 | 2002-01-24 | Merck Patent Gmbh | Chiral compounds i |
| ATE372314T1 (de) | 2000-07-13 | 2007-09-15 | Merck Patent Gmbh | Chirale verbindungen ii |
| JP2002201222A (ja) * | 2000-09-19 | 2002-07-19 | Merck Patent Gmbh | ポリマービーズ、ポリマービーズの使用方法、反射フィルム、セキュリティマーク、有価証券、セキュリティ装置 |
| JP2002363280A (ja) * | 2001-06-12 | 2002-12-18 | Chisso Corp | ポリアミド、これを用いた液晶配向剤ワニスおよび液晶表示素子 |
| US20030044690A1 (en) * | 2001-06-27 | 2003-03-06 | Imation Corp. | Holographic photopolymer data recording media, method of manufacture and method of holographically reading, recording and storing data |
-
2002
- 2002-12-11 DE DE10257711.0A patent/DE10257711B4/de not_active Expired - Lifetime
- 2002-12-23 US US10/326,150 patent/US7465479B2/en not_active Expired - Fee Related
- 2002-12-27 JP JP2002381295A patent/JP4553550B2/ja not_active Expired - Fee Related
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