KR880003894A - Optically Active Compounds and Liquid Crystal Compositions - Google Patents

Optically Active Compounds and Liquid Crystal Compositions Download PDF

Info

Publication number
KR880003894A
KR880003894A KR1019870006859A KR870006859A KR880003894A KR 880003894 A KR880003894 A KR 880003894A KR 1019870006859 A KR1019870006859 A KR 1019870006859A KR 870006859 A KR870006859 A KR 870006859A KR 880003894 A KR880003894 A KR 880003894A
Authority
KR
South Korea
Prior art keywords
carbon atoms
compound
group
oco
atom
Prior art date
Application number
KR1019870006859A
Other languages
Korean (ko)
Other versions
KR900004395B1 (en
Inventor
다쭈루 다보하시
다카오 사꾸라이
료이찌 히구찌
나오꼬 미까미
에리 야마모또
고지 다께우찌
Original Assignee
아지노모또 가부시끼가이샤
우따다 가쯔히로
아지노모또 가부시끼 가이샤
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by 아지노모또 가부시끼가이샤, 우따다 가쯔히로, 아지노모또 가부시끼 가이샤 filed Critical 아지노모또 가부시끼가이샤
Publication of KR880003894A publication Critical patent/KR880003894A/en
Application granted granted Critical
Publication of KR900004395B1 publication Critical patent/KR900004395B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/66Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
    • C07C69/67Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
    • C07C69/708Ethers
    • C07C69/712Ethers the hydroxy group of the ester being etherified with a hydroxy compound having the hydroxy group bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • 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
    • C07C43/21Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing rings other than six-membered aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Liquid Crystal Substances (AREA)

Abstract

내용 없음No content

Description

광학 활성 화합물 및 액정 조성물Optically Active Compounds and Liquid Crystal Compositions

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

제1도는 실시예1에서 수득된 광학 활성 사이클로프로판 화합물의 IR 스펙트럼.1 is an IR spectrum of the optically active cyclopropane compound obtained in Example 1.

제2도는 4'-옥틸카보닐옥시-4-(1S-2.2-디메틸사이클로-프로판메틸옥시카보닐)비페닐 및 4'-헵틸카보닐옥시-4-(1S-클로로-2-메틸부틸카보닐옥시)비페닐을 함유하는 조성물의 상다이어그램.Figure 2 shows 4'-octylcarbonyloxy-4- (1S-2.2-dimethylcyclo-propanemethyloxycarbonyl) biphenyl and 4'-heptylcarbonyloxy-4- (1S-chloro-2-methylbutylcarbon Phase diagram of a composition containing nyloxy) biphenyl.

Claims (11)

하기 일반식(1)의 광학 활성 사이클로프로판 화합물.Optically active cyclopropane compound of the following general formula (1). 상기식에서 R은 탄소수 4내지 18의 직쇄 또는 측쇄알킬 그룹 또는 탄소수 4 내지 18의 사이클로알킬 그룹이고, n은 0또는 1이며, Y4는 -CO2CH2-, -OCO- 또는 -OCH2-이고, Y1.Y2및 Y3는 독립적으로 -CO2-.-OCO-.-O-, 직접 결합 또는 -CH20-이며, Z1.Z2및 Z3는 독립적으로Wherein R is a straight or branched chain alkyl group having 4 to 18 carbon atoms or a cycloalkyl group having 4 to 18 carbon atoms, n is 0 or 1, and Y 4 is -CO 2 CH 2- , -OCO- or -OCH 2- Y 1 .Y 2 and Y 3 are independently -CO 2 -.- OCO -.- O-, a direct bond or -CH 2 0-, and Z 1 .Z 2 and Z 3 are independently 선택되고, Z1.Z2및 Z3로서 임의로 선택된 그룹중 적어도 2개는 같거나 다를 수 있고, A1·A2및 A3는 독립적으로 불소원자, 브롬원자, 염소원자, 시아노 그룹 또는 수소원자이며, C는 비대칭 탄소원자를 나타낸다.And at least two of the groups optionally selected as Z 1 .Z 2 and Z 3 may be the same or different, and A 1 A 2 and A 3 are independently a fluorine atom, bromine atom, chlorine atom, cyano group or A hydrogen atom, and C represents an asymmetric carbon atom. 제1항에 있어서, R이 탄소수 4내지 18의 직쇄 또는 측쇄알킬 그룹 또는 탄소수 4내지 18의 사이클로 알킬 그룹이고, n이 0이며, Y1이-CO2-이고, Y2가 직접 결합이며, Z1및 Z2가 1.4-페닐렌 그룹이고, Y4가-CO2CH2-인 광학 활성 사이클로프로판 화합물.2. The compound of claim 1, wherein R is a straight or branched chain alkyl group having 4 to 18 carbon atoms or a cycloalkyl group having 4 to 18 carbon atoms, n is 0, Y 1 is —CO 2 —, Y 2 is a direct bond, An optically active cyclopropane compound wherein Z 1 and Z 2 are 1.4-phenylene groups and Y 4 is —CO 2 CH 2 —. 제1항에 있어서, R이 탄소수 4내지 18의 직쇄 또는 측쇄알킬 그룹 또는 탄소수 4내지 18의 사이클로 알킬 그룹이고, n이 0이며, Y1이-0-이고, Y2가 직접결합이며, Z1및 Z2가 1.4-페닐렌 그룹을 나타내고, Y4가-OCO-을 나타내는 광학 활성 사이클로프로판 화합물.The compound of claim 1, wherein R is a straight or branched chain alkyl group having 4 to 18 carbon atoms or a cycloalkyl group having 4 to 18 carbon atoms, n is 0, Y 1 is 0-, Y 2 is a direct bond, and Z is Optically active cyclopropane compound in which 1 and Z 2 represent a 1.4-phenylene group and Y 4 represents —OCO—. 제1항에 있어서, R이 탄소수 4내지 18의 직쇄 또는 측쇄알킬 그룹 또는 탄소수 4내지 18의 사이클로 알킬 그룹이고, n이 0이며, Y1이 -COO-이고, Y2가 이중결합이며, Z1및 Z2가 1.4-페틸렌 그룹을 나타내고, Y4가-OCO-을 나타내는 광학 활성 사이클로프로판 화합물.2. The compound of claim 1, wherein R is a straight or branched chain alkyl group having 4 to 18 carbon atoms or a cycloalkyl group having 4 to 18 carbon atoms, n is 0, Y 1 is —COO—, Y 2 is a double bond, Z Optically active cyclopropane compound in which 1 and Z 2 represent a 1.4-petylene group and Y 4 represents —OCO—. 제1항에 있어서, R이 탄소수 4내지 18의 직쇄 또는 측쇄알킬 그룹 또는 탄소수 4내지 18의 사이클로 알킬 그룹이고, n이 0이며, Y1이 -OCOO-이고, Y2가 직접결합이며, Z1및 Z2가 1.4-페닐렌 그룹이고, Y4가-OCO-인 광학 활성 사이클로프로판 화합물. 2. The compound of claim 1, wherein R is a straight or branched chain alkyl group having 4 to 18 carbon atoms or a cycloalkyl group having 4 to 18 carbon atoms, n is 0, Y 1 is -OCOO-, Y 2 is a direct bond, and Z is Optically active cyclopropane compound wherein 1 and Z 2 are 1.4-phenylene groups and Y 4 is —OCO—. 제1항에 있어서, R이 탄소수 4내지 18의 직쇄 또는 측쇄알킬 그룹 또는 탄소수 4내지 18의 사이클로 알킬 그룹이고, n이 0이며, Y1이 -O-이고, Y2직접결합이며, Z1이 1.4-페닐렌그룹이고, Z2가 피리미딘-2.5-디일 그룹이며, Y4가 -OCO-인 광학 활성 사이클로프로판 화합물. 2. The compound of claim 1, wherein R is a straight or branched chain alkyl group having 4 to 18 carbon atoms or a cycloalkyl group having 4 to 18 carbon atoms, n is 0, Y 1 is —O—, Y 2 is a direct bond, and Z 1 This is a 1.4-phenylene group, Z <2> is a pyrimidine- 2.5 -diyl group, and Y <4> is -OCO-, The optically active cyclopropane compound. 제1항에 있어서, R이 탄소수 4내지 18의 직쇄 또는 측쇄알킬 그룹 또는 탄소수 4내지 18의 사이클로 알킬 그룹이고, n이 0이며, Y1이 직접결합이고, Y2가 직접 결합이며, Z1이 피라미딘-2.5-디일 그룹이고, Z2가 1.4-페닐렌 그룹이며, Y4가-OCO-인 광학 활성 사이클로프로판 화합물.2. The compound of claim 1, wherein R is a straight or branched chain alkyl group having 4 to 18 carbon atoms or a cycloalkyl group having 4 to 18 carbon atoms, n is 0, Y 1 is a direct bond, Y 2 is a direct bond, and Z 1 The optically active cyclopropane compound which is this pyramimid- 2.5 -diyl group, Z <2> is 1.4-phenylene group, and Y <4> -OCO-. 하기 일반식(1)의 광학 활성 사이클로프로판 화합물 적어도 하나 함유하는 액정 조성물.Liquid crystal composition containing at least one optically active cyclopropane compound of the following general formula (1). 상기식에서 R은 탄소수 4 내지 18의 직쇄 또는 측쇄알킬 그룹 또는 탄소수 4 내지 18의 사이클로알킬그룹이고, n은 0 또는 1이며, Y4는-CO2CH2-,-OCO-또는-OCH2-이고, Y1, Y2및 Y3는 독립적으로 -CO2-,-OCO-,-O-, 직접결합 또는-CH2O-이며, Z1,Z2및 Z3는 독립적으로Wherein R is a straight or branched chain alkyl group having 4 to 18 carbon atoms or a cycloalkyl group having 4 to 18 carbon atoms, n is 0 or 1, and Y 4 is -CO 2 CH 2- , -OCO- or -OCH 2- Y 1, Y 2 and Y 3 are independently —CO 2 —, — OCO —, — O—, a direct bond or —CH 2 O—, and Z 1 , Z 2 and Z 3 are independently 선택되고, Z1,Z2및 Z3로서 임의로 선택된 그룹중의 적어도 2개는 같거나 다를수 있고, A ㆍ A2및 A3는 독립적으로 불소원자, 브롬원자, 염소원자, 시아노그룹 또는 수소원자이며, C는 비대칭 탄소원자를 나타낸다.And at least two of the groups optionally selected as Z 1 , Z 2 and Z 3 may be the same or different and A. A 2 and A 3 are independently a fluorine atom, bromine atom, chlorine atom, cyano group or hydrogen An atom, and C represents an asymmetric carbon atom. 하기 일반식(1)의 광학 활성 사이클로프로판 화합물 및 이 화합물에 반대되는 콜레스테릭 나선형 피치를 갖는 액정 화합물 적어도 하나를 함유하는 유전성을 갖는 액정 조성물.A liquid crystal composition having dielectric properties containing at least one optically active cyclopropane compound of the general formula (1) and a liquid crystal compound having a cholesteric helical pitch opposite to the compound. 상기식에서 R은 탄소수 4 내지 18의 직쇄 또는 측쇄알킬 그룹 또는 탄소수 4내지 18의 사이클로알킬그룹이고, n은 0 또는 1이며, Y4는-CO2CH2-,-OCO-또는-OCH2-이고, Y1, Y2및 Y3는 독립적으로 -CO2-,-OCO-,-O-, 직접결합 또는-CH2O-이며, Z1,Z2및 Z3는 독립적으로Wherein R is a straight or branched chain alkyl group having 4 to 18 carbon atoms or a cycloalkyl group having 4 to 18 carbon atoms, n is 0 or 1, and Y 4 is -CO 2 CH 2- , -OCO- or -OCH 2- And Y 1 , Y 2 and Y 3 are independently —CO 2 —, — OCO —, — O—, a direct bond or —CH 2 O—, and Z 1 , Z 2 and Z 3 are independently 선택되고, Z1,Z2및 Z3로서 임의로 선택된 그룹중 적어도 2개는 같거나 다를수 있고, A1및 A2및 A3는 독립적으로 불소원자, 브롬원자, 염소원자, 시아노그룹 또는 수소원자이며, C는 비대칭 탄소원자를 나타낸다.And at least two of the groups optionally selected as Z 1 , Z 2 and Z 3 may be the same or different and A 1 and A 2 and A 3 are independently a fluorine atom, bromine atom, chlorine atom, cyano group or hydrogen An atom, and C represents an asymmetric carbon atom. 제9항에 있어서, 적어도 5㎛의 나선형 피치를 갖는 액정 조성물.10. The liquid crystal composition according to claim 9, having a helical pitch of at least 5 mu m. 제9항에 있어서, 광학적 활성을 갖지 않는 하나 이상의 스멕틱 C액정 화합물을 추가로 함유하고 적어도 5㎛의 나선형 피치를 갖는 액정 조성물.10. The liquid crystal composition according to claim 9, further containing at least one smectic C liquid crystal compound having no optical activity and having a spiral pitch of at least 5 μm. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019870006859A 1986-09-24 1987-07-01 Optically active compound and liquid crystalline composition KR900004395B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP225713 1986-09-24
JP22571386 1986-09-24

Publications (2)

Publication Number Publication Date
KR880003894A true KR880003894A (en) 1988-06-01
KR900004395B1 KR900004395B1 (en) 1990-06-25

Family

ID=16833639

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019870006859A KR900004395B1 (en) 1986-09-24 1987-07-01 Optically active compound and liquid crystalline composition

Country Status (1)

Country Link
KR (1) KR900004395B1 (en)

Also Published As

Publication number Publication date
KR900004395B1 (en) 1990-06-25

Similar Documents

Publication Publication Date Title
KR850001798A (en) Manufacturing Method of Liquid Crystal Dielectric
KR890008068A (en) Alkenylbicyclohexane
KR840007399A (en) Smectic Liquid Crystal Compound and Liquid Crystal Composition
ATE111882T1 (en) 2-SUBSTITUTED ALKYL ETHER AND LIQUID CRYSTAL COMPOSITION.
KR870700225A (en) Biphenyl Ester and Liquid Crystal Materials and Devices Containing the Same
KR900700439A (en) Laterally Fluorinated 4-cyanophenyl and 4&#39;-cyanobiphenyl benzoate
KR900009935A (en) Liquid crystal composition
ATE103888T1 (en) ETHANE DERIVATIVES.
KR880005122A (en) Chiral aryl-2,3-epoxyalkyl-ethers, the corresponding thio compounds and their use as dope paints in the liquid crystal phase
KR880011073A (en) Novel optically active compounds containing many asymmetric carbon atoms
KR890000627A (en) Smetic liquid crystal mixture
KR920701095A (en) Phenylcyclohexane and Liquid Crystal Medium
KR880006345A (en) Liquid crystal mixture
KR910700320A (en) Liquid crystal medium containing fluorinated oligophenyl
KR960000836A (en) Diene derivatives and liquid crystal media
KR890013159A (en) Ferroelectric Liquid Crystal Composition
KR900016190A (en) 2-phenylpyridine
EP0377516A3 (en) Liquid crystal compounds having high optical anisotropy
NO883048D0 (en) CHIRAL ARYLOXYPROPIONIC ACID ESTERS AND THEIR USE AS DOTATING IN LIQUID CRYSTAL PHASES.
KR900017974A (en) Liquid Crystal Component Containing Trimethyleneoxy Group
KR870010418A (en) Pyridine derivatives
KR900003095A (en) Alkoxymethylcyclohexane and alkenyloxymethylcyclohexane
KR940011410A (en) Conjugated Enine Derivatives and Liquid Crystal Compositions
KR920701379A (en) Liquid crystal medium
KR930010005A (en) Aromatic fatty acid esters

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
G160 Decision to publish patent application
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 19930622

Year of fee payment: 4

LAPS Lapse due to unpaid annual fee