JP2002517598A5 - - Google Patents
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- Publication number
- JP2002517598A5 JP2002517598A5 JP2000553530A JP2000553530A JP2002517598A5 JP 2002517598 A5 JP2002517598 A5 JP 2002517598A5 JP 2000553530 A JP2000553530 A JP 2000553530A JP 2000553530 A JP2000553530 A JP 2000553530A JP 2002517598 A5 JP2002517598 A5 JP 2002517598A5
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- JP
- Japan
- Prior art keywords
- diyl
- group
- independently
- different
- same
- 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
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- -1 cyclopropane -1 , 2-diyl Chemical group 0.000 description 84
- 229910052739 hydrogen Inorganic materials 0.000 description 24
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 22
- 239000001257 hydrogen Substances 0.000 description 22
- 125000004432 carbon atom Chemical group C* 0.000 description 21
- 125000000217 alkyl group Chemical group 0.000 description 16
- 125000003545 alkoxy group Chemical group 0.000 description 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 12
- 239000011159 matrix material Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- 0 C[*+]c1ccc(*)cc1F Chemical compound C[*+]c1ccc(*)cc1F 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 6
- 239000004973 liquid crystal related substance Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 4
- VQGHOUODWALEFC-UHFFFAOYSA-N 2-phenylpyridine Chemical compound C1=CC=CC=C1C1=CC=CC=N1 VQGHOUODWALEFC-UHFFFAOYSA-N 0.000 description 2
- COAQQCUYRRMZRF-UHFFFAOYSA-N Cc(ccc1cc(C)c2F)cc1c2F Chemical compound Cc(ccc1cc(C)c2F)cc1c2F COAQQCUYRRMZRF-UHFFFAOYSA-N 0.000 description 2
- CDWQZDHRPZSNQJ-UHFFFAOYSA-N Cc1ccc2c(F)c(C)ccc2c1 Chemical compound Cc1ccc2c(F)c(C)ccc2c1 CDWQZDHRPZSNQJ-UHFFFAOYSA-N 0.000 description 2
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 description 2
- 230000003098 cholesteric effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 1
- 125000005714 2,5- (1,3-dioxanylene) group Chemical group [H]C1([H])OC([H])([*:1])OC([H])([H])C1([H])[*:2] 0.000 description 1
- OXPDQFOKSZYEMJ-UHFFFAOYSA-N 2-phenylpyrimidine Chemical compound C1=CC=CC=C1C1=NC=CC=N1 OXPDQFOKSZYEMJ-UHFFFAOYSA-N 0.000 description 1
- TUYBTSCLNRYVED-UHFFFAOYSA-N 3,4-difluoro-2-phenylpyridine Chemical compound FC1=CC=NC(C=2C=CC=CC=2)=C1F TUYBTSCLNRYVED-UHFFFAOYSA-N 0.000 description 1
- UIYGBIMLYLGCSI-UHFFFAOYSA-N 4,6-difluoro-2-phenylpyrimidine Chemical compound FC1=CC(F)=NC(C=2C=CC=CC=2)=N1 UIYGBIMLYLGCSI-UHFFFAOYSA-N 0.000 description 1
- QOQLRJAGMWSOPK-UHFFFAOYSA-N 4-fluoro-2-phenylpyrimidine Chemical compound FC1=CC=NC(C=2C=CC=CC=2)=N1 QOQLRJAGMWSOPK-UHFFFAOYSA-N 0.000 description 1
- YESRKYFQGMCQIY-UHFFFAOYSA-N Cc(cc(c(C)c1)F)c1F Chemical compound Cc(cc(c(C)c1)F)c1F YESRKYFQGMCQIY-UHFFFAOYSA-N 0.000 description 1
- YLUCGURBBYPRDQ-UHFFFAOYSA-N Cc1ccc2c(F)c(C)c(F)cc2c1 Chemical compound Cc1ccc2c(F)c(C)c(F)cc2c1 YLUCGURBBYPRDQ-UHFFFAOYSA-N 0.000 description 1
- 239000004990 Smectic liquid crystal Substances 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- JVZRCNQLWOELDU-UHFFFAOYSA-N gamma-Phenylpyridine Natural products C1=CC=CC=C1C1=CC=NC=C1 JVZRCNQLWOELDU-UHFFFAOYSA-N 0.000 description 1
- 125000000466 oxiranyl group Chemical group 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1998125484 DE19825484A1 (de) | 1998-06-08 | 1998-06-08 | Monostabiles ferroelektrisches Aktivmatrix-Display |
| DE19830203.7 | 1998-07-07 | ||
| DE1998130203 DE19830203A1 (de) | 1998-07-07 | 1998-07-07 | Monostabiles ferroelektrisches Aktivmatrix-Display |
| DE19825484.9 | 1998-07-07 | ||
| PCT/EP1999/003939 WO1999064538A1 (de) | 1998-06-08 | 1999-06-08 | Monostabiles ferroelektrisches aktivmatrix-display |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002517598A JP2002517598A (ja) | 2002-06-18 |
| JP2002517598A5 true JP2002517598A5 (enExample) | 2006-09-07 |
| JP4713736B2 JP4713736B2 (ja) | 2011-06-29 |
Family
ID=26046671
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000553530A Expired - Fee Related JP4713736B2 (ja) | 1998-06-08 | 1999-06-08 | 単安定強誘電性アクティブマトリックスディスプレイ |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6551668B1 (enExample) |
| EP (1) | EP1086194B1 (enExample) |
| JP (1) | JP4713736B2 (enExample) |
| KR (1) | KR100616271B1 (enExample) |
| DE (1) | DE59905658D1 (enExample) |
| WO (1) | WO1999064538A1 (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19922723A1 (de) * | 1999-05-18 | 2000-11-23 | Clariant Gmbh | Aktivmatrix-Displays mit hohem Kontrast |
| GB0024487D0 (en) * | 2000-10-05 | 2000-11-22 | Koninkl Philips Electronics Nv | Bistable chiral nematic liquid crystal display and method of driving the same |
| US6824707B2 (en) | 2001-10-23 | 2004-11-30 | Clariant International Ltd. | Active matrix liquid crystal device and smectic liquid crystal mixture |
| EP1591512A1 (en) * | 2004-04-26 | 2005-11-02 | AZ Electronic Materials (Germany) GmbH | Chiral smectic liquid crystal mixture |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4367924A (en) | 1980-01-08 | 1983-01-11 | Clark Noel A | Chiral smectic C or H liquid crystal electro-optical device |
| DE3068983D1 (en) | 1980-01-10 | 1984-09-27 | Noel A Clark | Chiral smectic liquid crystal electro-optical device and process of making the same |
| EP0573878B1 (de) * | 1992-06-09 | 2000-12-20 | Aventis Research & Technologies GmbH & Co. KG | 3-Fluorpyridine, Verfahren zu ihrer Herstellung und ihre Verwendung in Flüssigkristallmischungen |
| JPH08151579A (ja) * | 1994-11-29 | 1996-06-11 | Sumitomo Chem Co Ltd | 液晶組成物およびこれを含む液晶素子 |
| KR19990029052A (ko) | 1995-07-17 | 1999-04-15 | 악커만 요아힘, 되르 클라우스 | 강유전성 액정 혼합물 |
| JPH10510066A (ja) | 1995-09-25 | 1998-09-29 | フィリップス エレクトロニクス ネムローゼ フェンノートシャップ | 表示装置 |
| DE19732381A1 (de) * | 1997-07-25 | 1999-01-28 | Hoechst Ag | Ferroelektrische Flüssigkristallanzeige mit aktiven Matrix Elementen |
| EP0916713A1 (en) * | 1997-10-28 | 1999-05-19 | Aventis Research & Technologies GmbH & Co. KG | Chiral smectic liquid crystal mixture containing 1,3-difluoronaphthalenes |
| EP0916715A1 (en) * | 1997-11-11 | 1999-05-19 | Aventis Research & Technologies GmbH & Co. KG | Chiral smectic liquid crystal mixture containing compounds with fluorinated sidechains |
-
1999
- 1999-06-08 DE DE59905658T patent/DE59905658D1/de not_active Expired - Lifetime
- 1999-06-08 KR KR1020007013950A patent/KR100616271B1/ko not_active Expired - Fee Related
- 1999-06-08 EP EP99929151A patent/EP1086194B1/de not_active Expired - Lifetime
- 1999-06-08 JP JP2000553530A patent/JP4713736B2/ja not_active Expired - Fee Related
- 1999-06-08 WO PCT/EP1999/003939 patent/WO1999064538A1/de not_active Ceased
- 1999-06-08 US US09/719,028 patent/US6551668B1/en not_active Expired - Lifetime
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