KR890700555A - 톨란류 - Google Patents

톨란류

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Publication number
KR890700555A
KR890700555A KR1019880701560A KR880701560A KR890700555A KR 890700555 A KR890700555 A KR 890700555A KR 1019880701560 A KR1019880701560 A KR 1019880701560A KR 880701560 A KR880701560 A KR 880701560A KR 890700555 A KR890700555 A KR 890700555A
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Prior art keywords
phenylene
group
radicals
substituted
groups
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KR1019880701560A
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English (en)
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KR920000415B1 (ko
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라이펜라트 폴커
크라우세 요아힘
게오르그베버
히티히 라인하르트
Original Assignee
나우만, 호이만
메르크 파렌트 게젤샤프트 미트 베슈랭크터 하프퉁
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Priority claimed from PCT/EP1987/000515 external-priority patent/WO1988002130A2/de
Priority claimed from PCT/DE1988/000133 external-priority patent/WO1988007514A1/de
Application filed by 나우만, 호이만, 메르크 파렌트 게젤샤프트 미트 베슈랭크터 하프퉁 filed Critical 나우만, 호이만
Publication of KR890700555A publication Critical patent/KR890700555A/ko
Application granted granted Critical
Publication of KR920000415B1 publication Critical patent/KR920000415B1/ko

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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C15/00Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
    • C07C15/40Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals
    • C07C15/50Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals polycyclic non-condensed
    • C07C15/54Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals polycyclic non-condensed containing a group with formula
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C25/00Compounds containing at least one halogen atom bound to a six-membered aromatic ring
    • C07C25/24Halogenated aromatic hydrocarbons with unsaturated side chains
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00Ethers; Compounds having groups, groups or groups
    • C07C43/02Ethers
    • C07C43/20Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
    • C07C43/215Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring having unsaturation outside the six-membered aromatic rings
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    • C07C43/00Ethers; Compounds having groups, groups or groups
    • C07C43/02Ethers
    • C07C43/20Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
    • C07C43/225Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
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    • C09K19/02Liquid crystal materials characterised by optical, electrical or physical properties of the components, in general
    • C09K19/0216Super Birefringence Effect (S.B.E.); Electrically Controlled Birefringence (E.C.B.)
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    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/10Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
    • C09K19/12Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
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    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/10Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
    • C09K19/14Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain
    • C09K19/18Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a carbon chain the chain containing carbon-to-carbon triple bonds, e.g. tolans
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    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/30Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
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    • C09K19/30Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
    • C09K19/3001Cyclohexane rings
    • C09K19/3066Cyclohexane rings in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers
    • C09K19/3068Cyclohexane rings in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers chain containing -COO- or -OCO- groups
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    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/34Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
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    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/34Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
    • C09K19/3402Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having oxygen as hetero atom
    • C09K2019/3422Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having oxygen as hetero atom the heterocyclic ring being a six-membered ring

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Liquid Crystal Substances (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

내용 없음.

Description

톨란류
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (10)

  1. 일반식(I)의 톨란류.
    상기식에서, R1과 R2는 상호 각기 독립적으로 하나 또는 두 개의 비인접 CH2또는 CF2그룹이-O-에 의해 치환될 수 있는 탄소수 15이하의 알킬 또는 퍼플루오로알킬이고, 또한 라디칼 R1과 R2중 하나는 할로겐, -CH, -NC, -N3또는 -NCS이고, A1과 A2는 상호 각기 독립적으로 비치환 또는 할로겐 및/또는 니트릴에 의해 일치환 또는 다치환된 1,4-페닐렌(여기에서 하나 또는 그이상의 CH그룹은 또한 N으로 치환될 수 있다), 1, 4-비시클로(2.2.2)옥틸렌 또는 트렌스-1, 4-시클로헥실렌(여기에서 하나 또는 두개의 비인접 CH2그룹은 -O- 및/또는 -S원자에 의해 치환될 수도 있다)이고, Z1은 -CH2CH2-, -CH2O-, -CO-O-, -OCH2-, -O-CO- 또는 단일 결합이고, m과 n은 상호 각기 독립적으로 O 또는 1이고, A3및 A4는 상호각기 독립적으로 비치환 또는 할로겐 및/또는 니트릴에 의해 일치환 또는 다치환된 1, 4-페닐렌이고, 단, 둘중 하나는 2, 3-디할로게노-1, 4-페닐렌 그룹을 함유하거나, a) m=n=0이고, A3와 A4는 비치환된 1, 4-페닐렌이며, R1은 알콕시 그룹이고, R2는 불소, -NC, -N3또는 -NCS이거나 라디칼 R1과 R2중 하나는 적어도 두개의 CH2그룹이 -O-에 의해 치환된 알킬 그룹 또는, 라티칼 R1과 R2중 하나는 퍼플루오로알킬 그룹 또는 -OCF3이거나, B) m=n=0이고, A3및/또는 A4는 일치환 1, 4-페닐렌이면, 라티칼 R1과 R2중 적어도 하나는 -CN, -NC, -N3, -NCS, OCF3또는 퍼플루오로알킬이거나, C) A3와 A4는 비치환된 1, 4-페닐렌, n=0 또는 1, m=1, 및 Z1은 단일 결합이면, 라디칼 R1과 R2중 하나는 알콕시 그룹이고 이때 나머지는 할로겐, 알킬, -CN, -NC, N3또는 NCS이거나, 라티칼 R1과 R2중 하나는 퍼를루오로알킬 또는 -OCF3이거나, d) A3와 A4가 비치환된 1, 4-페닐렌이고, n=0, m-1 및 Z1은 -CO-O-이면, R1과 R2중 하나는 알콕시 그룹이고, 나머지 하나는 할로겐, 알킬, -NC, N3또는 NCS이거나, 라디칼 R1과 R2중 하나는 퍼플루오로알킬 그룹 또는 -OCF3이거나, e) m=0, n=1이고, 그룹 A2, A3또는 A4중 하나가 일치환된 1, 4-페닐렌이고, 나머지 두 그룹이 1, 4-페닐렌이면 그룹 A3와 A4중 하나는 일치환된 1, 4-페닐렌 그룹이다.
  2. 제1항에 있어서, 그룹 A1, A2, A3및 A4중 적어도 하나가 2, 3-디할로게노 -1, 4-페닐렌 그룹인 일반식(I)의 톨란류.
  3. 제1항에 있어서, m은 0이고, n은 1이며, R1은 알콕시 그룹이고, R2는 알킬 그룹이고, A2는 1, 4-시클로헥실렌 그룹이며 그리고 A3와 A4는 각기 상호 독립적으로 비치환 또는 할로겐 및/또는 니트릴로 일치환 또는 다치환된 1, 4-페닐렌인 일반식(I)의 톨란류.
  4. 제3항에 있어서, R1이 탄소수 1 내지 7인 직쇄 알콕시 그룹이고, R2가 탄소수 1 내지 7인 직쇄알킬 그룹인 일반식(I)의 톨란류.
  5. 제1항의 일반식(I)의 화합물을 적어도 1종 함유하는 엑정상 성분 적어도 2종을 갖는 엑정상.
  6. 엑정상 성분으로서 제1항의 일반식(I)의 화합물의 용도.
  7. ECS 효과에 의거하는 전-광 디스플레이 소자용 엑정상의 성분으로서 제1항의 일반식(I)의 화합물의 용도.
  8. 제1항의 일반식(I)의 화합물을 적어도 1종 함유하는 엑정상 성분 적어도 2종을 갖는 ECB 효과에 의거하는 전-광 디스플레이 소자용 엑정상.
  9. 제5항의 엑정상을 엑정 유전체로서 함유하는 전-광 디스플레이 소자.
  10. 제8항에 상을 유전체로서 함유하는 ECB 효과에 의거한 전-광 디스플레이 소자.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019880701560A 1987-04-03 1988-11-29 톨란류 KR920000415B1 (ko)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
DE19873711306 DE3711306A1 (de) 1987-04-03 1987-04-03 Tolanderivate und verwendung von carbonitrilen in fluessigkristallinen phasen fuer anzeigeelemente basierend auf dem ecb-effekt
DEP3711306.2 1987-04-03
PCT/EP1987/000515 WO1988002130A2 (en) 1986-09-16 1987-09-09 Liquid crystal phases for electro-optic display elements based on the ecb effect
EPPCT/EP/87/00515 1987-09-09
EPPCT/EP87/00515 1987-09-09
PCT/DE1988/000133 WO1988007514A1 (en) 1987-04-03 1988-03-10 Tolanes

Publications (2)

Publication Number Publication Date
KR890700555A true KR890700555A (ko) 1989-04-25
KR920000415B1 KR920000415B1 (ko) 1992-01-13

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DE (1) DE3711306A1 (ko)
SG (1) SG28348G (ko)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100273604B1 (ko) * 1992-11-16 2000-12-15 플레믹 크리스티안 플루오르 치환된 톨란 유도체

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4143657B4 (de) * 1991-02-23 2007-11-22 Merck Patent Gmbh Flüssigkristalline Medien enthaltend 2,6-Difluortolane sowie deren Verwendung in elektrooptischen Anzeigen
DE4105742C2 (de) * 1991-02-23 2001-08-09 Merck Patent Gmbh 2,6 Difluortolane und deren Verwendung als Komponenten flüssigkristalliner Medien
DE4218614B4 (de) * 1992-06-05 2005-07-21 Merck Patent Gmbh Benzolderivate

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100273604B1 (ko) * 1992-11-16 2000-12-15 플레믹 크리스티안 플루오르 치환된 톨란 유도체

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SG28348G (en) 1995-09-18
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