KR880014079A - 액정혼합물중의 도핑제로서 광학적으로 활성인 옥시란-2-카복실산 에스테르의 용도 - Google Patents
액정혼합물중의 도핑제로서 광학적으로 활성인 옥시란-2-카복실산 에스테르의 용도 Download PDFInfo
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- KR880014079A KR880014079A KR1019880006307A KR880006307A KR880014079A KR 880014079 A KR880014079 A KR 880014079A KR 1019880006307 A KR1019880006307 A KR 1019880006307A KR 880006307 A KR880006307 A KR 880006307A KR 880014079 A KR880014079 A KR 880014079A
- Authority
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- South Korea
- Prior art keywords
- carboxylic acid
- general formula
- acid ester
- optically active
- liquid crystal
- Prior art date
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- OTGHWLKHGCENJV-UHFFFAOYSA-N glycidic acid Chemical class OC(=O)C1CO1 OTGHWLKHGCENJV-UHFFFAOYSA-N 0.000 title claims 9
- 239000004973 liquid crystal related substance Substances 0.000 title claims 6
- 239000000203 mixture Substances 0.000 title claims 6
- 239000002019 doping agent Substances 0.000 title claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 4
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 150000001733 carboxylic acid esters Chemical class 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 238000010586 diagram Methods 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052717 sulfur Chemical group 0.000 claims 1
- 239000011593 sulfur Chemical group 0.000 claims 1
Classifications
-
- 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
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/10—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
- C09K19/20—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters or ethers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/48—Compounds containing oxirane rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms, e.g. ester or nitrile radicals
-
- 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
-
- 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
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/137—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering
- G02F1/139—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering based on orientation effects in which the liquid crystal remains transparent
- G02F1/141—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering based on orientation effects in which the liquid crystal remains transparent using ferroelectric liquid crystals
- G02F1/1418—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering based on orientation effects in which the liquid crystal remains transparent using ferroelectric liquid crystals using smectic liquid crystals, e.g. based on the electroclinic effect
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/35—Non-linear optics
- G02F1/355—Non-linear optics characterised by the materials used
- G02F1/361—Organic materials
- G02F1/3615—Organic materials containing polymers
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/35—Non-linear optics
- G02F1/37—Non-linear optics for second-harmonic generation
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- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Nonlinear Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Optics & Photonics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Liquid Crystal Substances (AREA)
- Epoxy Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- 액정혼합물중의 도핑제(dopant)로서 사용되는 광학적으로 활성인 옥시란-2-카복실산 에스테르의 용도.
- 제 1 항에 있어서, 일반식(Ⅰ)의 옥시란-2-카복실산 에스테르의 용도.상기식에서,또는 1 내지 16개의 탄소원자를 함유하는 직쇄 또는 측쇄 알킬 라디칼 또는 3내지 16개의 탄소원자를 함유하는 직쇄 또는 측쇄 알케닐라디칼이며, 이때 상기 라디칼 자체는 비대칭 탄소원자를 함유할 수 있으며, 인접하지 않은 -CH2그룹중의 하나 이상은 -O-, -S-, -CO-, -O-CO- 및/또는 -CO-O-로 대체될 수 있고, 하나 이상의 수소원자는 F, CL, B2또는 CN으로 대체될 수 있으며, R2는 수소 또는 1 내지 16개의 탄소원자를 함유 하는 알킬, 또는 각각의 경우 4또는 4'위치가 1 내지 16개의 탄소원자를 함유하는 알킬 쇄로 치환될 수 있는 사이클로헥실 또는 비사이클로 헥실이고, R3는 수소 또는 1 내지 16개의 탄소원자를 함유하는 알킬이고, J 및 1은 0, 1 또는 2 이고, K 및 m은 0또는 1이고, n은 0, 1또는 2이며, 단, j 및/또는 1이 0이면 K는 0 이고 ; n이 0이면 m은 0이고 ; J+1-n의 합은 최소한 1이고 최대한 3이며,-A1, -A2는이고,-A3는이고,-M1, M2는 -CO-0, -0-CO, -CH2CH2, -CH=CH, -CH2O, -OCH2이고 X는 산소 또는 황이다.
- 제 2 항에 있어서, 일반식(Ⅳ)의 옥시란-2-카복실산 에스테르의 용도.상기식에서, R4는 비대칭 탄소원자를 함유할 수 있는, 탄소수 6 내지 12의 직쇄 또는 측쇄 알킬 또는 알케닐 라디칼을 나타내고 ; -M3-O, -S, -O-CO 또는 -CO를 나타내고를 나타낸다.
- 제 2 항에서 청구된 일반식(Ⅰ)의 광학적으로 활성인 옥시란-2-카복실산 에스테르.
- 제 3 항에서 청구된 일반식(Ⅳ)의 광학적으로 활성인 옥시란 -2-카복실산에스테르.
- 적어도 하나의 광학적으로 활성인 록시란 -2-카복실산 에스테르르를 함유하는 액정혼합물.
- 제 2 항에서 청구된 적어도 하나의 일반식(Ⅰ)의 광학적으로 활성인 옥시란 -2-카복실산 에스테르를 함유하는 액정혼합물.
- 제 3 항에서 청구된 적어도 하나의 일반식(Ⅳ)의 광학적으로 옥시란-2-카복실산 에스트레르를 함유하는 액정혼합물.
- 제 6 항에 있어서 청구된 액정혼합물의 함유하는 전자 광학적 스위칭 도는 디스플레이 부품.
- 일반식(Ⅱ)의 메소제닉 페놀 또는 티오페놀을 일반식(Ⅲ)의 옥시란-2-카복실산 유도체와 반응시켜, 제 2 항에서 청구된 일반식(Ⅰ)의 광학적으로 활성인 옥시란-2-카복실산 에스테르를 제조하는 방법.R1(-A1)i(-M1)j(-A2)1(-M2)m(-A3)n-X-H상기식에서, R1,R2,R3, -A1, J. -M1, K, -A2, 1, -M2, m, -A3, n 및 X는 제 2 항에서 정의한 의미를 가지며 Y는 OH 그룹 또는 할로겐을 나타낸다.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP3718174.2 | 1987-05-29 | ||
DE19873718174 DE3718174A1 (de) | 1987-05-29 | 1987-05-29 | Verwendung von optisch aktiven oxiran-2-carbonsaeureestern als dotierstoffe in fluessigkristallmischungen, diese enthaltende fluessigkristallmischungen und neue optisch aktive oxiran-2-carbonsaeureester |
Publications (2)
Publication Number | Publication Date |
---|---|
KR880014079A true KR880014079A (ko) | 1988-12-22 |
KR960006076B1 KR960006076B1 (ko) | 1996-05-08 |
Family
ID=6328718
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019880006307A KR960006076B1 (ko) | 1987-05-29 | 1988-05-28 | 광학 활성 옥시란-2-카복실산 에스테르, 이를 함유하는 액정 혼합물 및 액정 혼합물에서 도핑제로서의 광학 활성 옥시란 2-카복실산 에스테르의 용도 |
Country Status (8)
Country | Link |
---|---|
US (1) | US4988459A (ko) |
EP (1) | EP0292954B1 (ko) |
JP (1) | JPH072728B2 (ko) |
KR (1) | KR960006076B1 (ko) |
AT (1) | ATE89029T1 (ko) |
DE (2) | DE3718174A1 (ko) |
ES (1) | ES2056855T3 (ko) |
NO (1) | NO882353L (ko) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0257048B1 (de) * | 1986-02-17 | 1994-08-24 | MERCK PATENT GmbH | Optisch aktive verbindungen |
US5354500A (en) * | 1986-05-29 | 1994-10-11 | Hoechst Aktiengesellschaft | Optically active carboxylic esters of oxygen-containing heterocycles as doping substances in liquid crystal mixtures and liquid crystal mixtures containing them |
US5676880A (en) * | 1987-09-18 | 1997-10-14 | Rolic Ag | Ferroelectric liquid crystal cell |
DE3876059D1 (de) * | 1987-09-18 | 1992-12-24 | Hoffmann La Roche | Ferroelektrische fluessigkristallzelle. |
GB8812427D0 (en) * | 1988-05-25 | 1988-06-29 | Merck Patent Gmbh | Electroclinic mixtures |
US5637254A (en) * | 1988-07-08 | 1997-06-10 | Hoechst Aktiengesellschaft | Ferroelectric liquid-crystalline polymers, a process for their preparation and their use in electrooptical components |
DE3832503A1 (de) * | 1988-09-24 | 1990-03-29 | Hoechst Ag | Neue optisch aktive ester der 5-ethyl- und der 5-vinyl-1,3-dioxolan-4-carbonsaeure, ihre verwendung als dotierstoffe in fluessigkristallmischungen und die neuen ester enthaltende fluessigkristallmischungen |
DE68926901T2 (de) * | 1988-10-19 | 1997-01-02 | Matsushita Electric Ind Co Ltd | Ferroelektrische Flüssigkristallmischung und Flüssigkristallanzeigevorrichtung |
DE3909356A1 (de) * | 1989-03-22 | 1990-09-27 | Hoechst Ag | Fluessigkristalline, insbesondere ferroelektrische fluessigkristalline mischungen |
JP2984322B2 (ja) * | 1990-06-06 | 1999-11-29 | キヤノン株式会社 | 液晶組成物およびこれを含む液晶素子 |
DE4023027A1 (de) * | 1990-07-20 | 1992-01-23 | Hoechst Ag | Chirale alken-aryl-2,3-epoxyalkyl-ether und ihre verwendung in fluessigkristallinen mischungen |
DE4120783A1 (de) * | 1991-06-24 | 1993-01-07 | Hoechst Ag | Optisch aktive oxiranderivate und ihre verwendung als dotierstoffe in fluessigkristallmischungen |
DE4211563A1 (de) * | 1992-04-07 | 1993-10-14 | Hoechst Ag | Chirale Oxiranderivate und ihre Verwendung als Dotierstoffe in Flüssigkristallmischungen |
DE4304756C1 (de) * | 1993-02-17 | 1994-09-08 | Hoechst Ag | Verfahren zur Darstellung von Salzen, chiraler, alpha-sauerstoffunktionalisierter Carbonsäuren |
DE4311967A1 (de) * | 1993-04-10 | 1994-10-13 | Hoechst Ag | Smektische Flüssigkristallmischung |
DE4311968A1 (de) * | 1993-04-10 | 1994-10-20 | Hoechst Ag | Smektische Flüssigkristallmischung |
US5387657A (en) * | 1993-09-10 | 1995-02-07 | The Dow Chemical Company | Epoxy resins containing thiadiazole and/or oxadiazole moieties |
DE19732160A1 (de) | 1997-07-25 | 1999-01-28 | Hoechst Ag | Chipkarte mit bistabiler Anzeige |
WO2010116990A1 (ja) * | 2009-04-10 | 2010-10-14 | 日産化学工業株式会社 | ケージ状シクロペンタン酸二無水物化合物、その製造法およびポリイミド |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60218358A (ja) * | 1984-04-13 | 1985-11-01 | Ajinomoto Co Inc | 液晶 |
US4705874A (en) * | 1985-10-01 | 1987-11-10 | University Patents, Inc. | Synthesis of new liquid crystal materials possessing phenylbenzoate or biphenyl core units and (2,3)-epoxyalkyloxiranemethanol chiral tails |
US4638073A (en) * | 1985-10-01 | 1987-01-20 | Walba David M | Synthesis of new liquid crystal materials possessing phenylbenzoate or biphenyl core units and (2,3)-epoxyalkyloxiranemethanol chiral tails |
US4789751A (en) * | 1985-10-01 | 1988-12-06 | University Patents, Inc. | Synthesis of new liquid crystal materials possessing phenylbenzoate or biphenyl core units and (2,3)-epoalkyloxirane methanol chiral tails |
EP0244129B1 (en) * | 1986-04-21 | 1992-11-11 | Ajinomoto Co., Inc. | Optically active compound and liquid crystalline composition |
DE3731619A1 (de) * | 1986-10-01 | 1988-04-14 | Merck Patent Gmbh | Stickstoffhaltige verbindungen zur verwendung in fluessigkristallinen mischungen |
DE3633968A1 (de) * | 1986-10-06 | 1988-04-07 | Hoechst Ag | Chirale aryl-2,3-epoxyalkyl-ether und deren entsprechende thioverbindungen und ihre verwendung als dotierstoff in fluessigkristall-phasen |
DE3886087D1 (de) * | 1987-04-07 | 1994-01-20 | Hoechst Ag | Verwendung von Verbindungen oder Gemischen von Verbindungen, die eine chirale, orthogonale, höher geordnete smektische Phase aufweisen, im Bereich dieser Phase als Schalt- oder Anzeigemedium. |
EP0307880B1 (de) * | 1987-09-19 | 1994-01-12 | Hoechst Aktiengesellschaft | Flüssigkristalline, insbesondere ferroelektrische flüssigkristalline Mischungen |
US4835295A (en) * | 1987-09-21 | 1989-05-30 | The University Of Colorado Foundation, Inc. | Ferroelectric liquid crystal compounds and compositions |
CN1022409C (zh) * | 1987-11-25 | 1993-10-13 | 赫彻斯特股份公司 | 液晶环丙基烷基杂环化合物制备方法 |
-
1987
- 1987-05-29 DE DE19873718174 patent/DE3718174A1/de not_active Withdrawn
-
1988
- 1988-05-26 ES ES88108381T patent/ES2056855T3/es not_active Expired - Lifetime
- 1988-05-26 US US07/199,101 patent/US4988459A/en not_active Expired - Lifetime
- 1988-05-26 DE DE8888108381T patent/DE3880734D1/de not_active Expired - Fee Related
- 1988-05-26 EP EP88108381A patent/EP0292954B1/de not_active Expired - Lifetime
- 1988-05-26 AT AT88108381T patent/ATE89029T1/de not_active IP Right Cessation
- 1988-05-27 NO NO882353A patent/NO882353L/no unknown
- 1988-05-27 JP JP63128608A patent/JPH072728B2/ja not_active Expired - Lifetime
- 1988-05-28 KR KR1019880006307A patent/KR960006076B1/ko not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
US4988459A (en) | 1991-01-29 |
JPH072728B2 (ja) | 1995-01-18 |
EP0292954A2 (de) | 1988-11-30 |
DE3880734D1 (de) | 1993-06-09 |
EP0292954B1 (de) | 1993-05-05 |
DE3718174A1 (de) | 1988-12-15 |
ES2056855T3 (es) | 1994-10-16 |
NO882353D0 (no) | 1988-05-27 |
ATE89029T1 (de) | 1993-05-15 |
EP0292954A3 (en) | 1989-08-30 |
NO882353L (no) | 1988-11-30 |
KR960006076B1 (ko) | 1996-05-08 |
JPS63310879A (ja) | 1988-12-19 |
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