JPS6047093A - Liquid crystal composition - Google Patents

Liquid crystal composition

Info

Publication number
JPS6047093A
JPS6047093A JP15364183A JP15364183A JPS6047093A JP S6047093 A JPS6047093 A JP S6047093A JP 15364183 A JP15364183 A JP 15364183A JP 15364183 A JP15364183 A JP 15364183A JP S6047093 A JPS6047093 A JP S6047093A
Authority
JP
Japan
Prior art keywords
liquid crystal
formula
cholesteryl
cholesteric liquid
ratio
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.)
Pending
Application number
JP15364183A
Other languages
Japanese (ja)
Inventor
Akihiro Mochizuki
昭宏 望月
Yoshizumi Ikegami
池上 佳住
Toshiaki Narisawa
成沢 俊明
Hirofumi Okuyama
奥山 弘文
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujitsu Ltd
Original Assignee
Fujitsu Ltd
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 Fujitsu Ltd filed Critical Fujitsu Ltd
Priority to JP15364183A priority Critical patent/JPS6047093A/en
Publication of JPS6047093A publication Critical patent/JPS6047093A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/36Steroidal liquid crystal compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • 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
    • C09K19/24Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing nitrogen-to-nitrogen bonds
    • C09K19/26Azoxy compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • 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
    • C09K19/30Non-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
    • C09K19/3003Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/42Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40

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  • Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Liquid Crystal Substances (AREA)

Abstract

PURPOSE:To provide a liquid crystal compsn. consisting of specified cyclohexane, azoxy and compensation type cholesteric liquid crystals and cholesteryl nonanoate, which makes high speed input possible and has a short transient turbidity time in transition to a storage state. CONSTITUTION:The liquid crystal compsn. is prepd. by blending (A) cyclohexane liquid crystal of formula I (where R1 is 1-7C straight chain alkyl or straight chain alkoxyl), (B) azoxy liquid crystal of formula II and/or III (where R2 is 1-7C alkyl or alkoxyl; R3 is R1 or cyano), (C) compensation type cholesteric liquid crystal consisting of a mixt. of cholesteryl myristenite of formula IV and cholesteryl chloride of formula V in a blend ratio of 1-1.75:1 by weight and (D) cholesteryl nonanoate of formula VI, with (C) and (D) contained each in 6- 10wt% and used in a ratio of 2:3 or lower. EFFECT:The liquid crystal compsn. makes it possible to perform high speed input in less than 10sec and controls transient turbidity time in transition to storage state to less than 3sec.

Description

【発明の詳細な説明】 (1)発明の技術分野 本発明は蓄積型液晶表示用液晶材料に係り、特に書き込
みを10m5以下の高速で実行し、なおかつ蓄積状態に
以降する際に発生する一時的白濁の時間を短くすること
ができる液晶組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION (1) Technical Field of the Invention The present invention relates to a liquid crystal material for an accumulation type liquid crystal display, and in particular to a liquid crystal material for an accumulation type liquid crystal display, and in particular to a liquid crystal material for storage type liquid crystal display. The present invention relates to a liquid crystal composition that can shorten the period of clouding.

(2)技術の背景 正の誘電異方性を有する液晶は電界電圧を該液晶に印加
するにつれて透明状態から白濁状態へと以降し、そしで
ある電圧に達すると再び透明状態となる。この透明状態
は印加している電圧を急激に取り去ることによって最初
の透明状態に戻すことが出来る。正の誘電異方性を有す
る蓄積型液晶は電界電圧がゼロの時に2つの安定状態、
すなわら、白濁仄態及び透明状態を任意に選択し得ると
いう点で1+5徴的である。
(2) Background of the Technology A liquid crystal having positive dielectric anisotropy changes from a transparent state to a cloudy state as an electric field voltage is applied to the liquid crystal, and then becomes transparent again when a certain voltage is reached. This transparent state can be returned to the initial transparent state by rapidly removing the applied voltage. Storage type liquid crystals with positive dielectric anisotropy have two stable states when the electric field voltage is zero:
In other words, it is characteristic of 1+5 in that the cloudy state and the transparent state can be arbitrarily selected.

ネマティック−コレステリック相転移を利用した誘電率
異方性が正を示すM積型液晶表示ば第1図に示すような
印加電圧−光透過率の関係を利用して行われる。
An M-type liquid crystal display with positive dielectric anisotropy utilizing nematic-cholesteric phase transition is produced by utilizing the relationship between applied voltage and light transmittance as shown in FIG.

まず電界が印加されない時は、図1中Gの状態にあり透
明である。これに電圧を除々に加えていくと液晶層は白
濁してFの状態になる。
First, when no electric field is applied, it is in the state G in FIG. 1 and is transparent. When a voltage is gradually applied to this, the liquid crystal layer becomes cloudy and enters the F state.

更に電圧を加えていきVl、1以上の電圧を加えること
によって液晶は透明なH状態になる。ここでG、、Fの
状態はともにコレステリック相でありH状態はネマティ
ック相である。すなわちVHO上の電圧印加によって液
晶はコレステリック相からネマティック相へ相転移する
By further applying a voltage to Vl, the liquid crystal becomes a transparent H state by applying a voltage of 1 or more. Here, the states G, , and F are both in the cholesteric phase, and the state H is in the nematic phase. That is, by applying a voltage on the VHO, the liquid crystal undergoes a phase transition from a cholesteric phase to a nematic phase.

相転移後のHまたは1]′状態が書き込みを行える状態
であるため、G−F−Hの変化を初期化と呼んでいる。
Since the H or 1]' state after the phase transition is a state in which writing can be performed, the change in G-F-H is called initialization.

蓄積型液晶表示は、このl]または11′状態から電圧
をゼロにしてG(透明:非選択)またばFo (/!3
二選択)へそれぞれ状態を変化させ書き込みを行う。こ
の時初期化状態を保っておくために必要な電圧が駆動電
圧■oであり■いとは2Vo首V+という関係を持って
いる。
In the storage type liquid crystal display, the voltage is zeroed from this l] or 11' state and G (transparent: not selected) or Fo (/!3
2 selections), change the state and write to each. At this time, the voltage required to maintain the initialized state is the driving voltage (2), and (2) and (2) have a relationship of 2Vo and V+.

尚、透明な初期化状態HまたはH′から、透明な安定状
jD Qへ移行する時には実際にはH(H’)−F−G
という経路をとる。そのため蓄積型液晶表示では原理的
に画面定着時に数秒間の白濁を生ずる。
Note that when transitioning from the transparent initial state H or H' to the transparent stable state jDQ, actually H(H')-F-G
Take that route. Therefore, in principle, in storage type liquid crystal displays, cloudiness occurs for several seconds when the screen is fixed.

(3)従来技術と問題点 従来の蓄積型液晶は書き込み時間が20〜401naで
あり、数msで書き込める組成もあることはあったが蓄
積状態移行時の一時的白濁時間が長く、)ルぎ込のを速
く行っても、全体としては表示に長い時間をかけるとい
う欠点がある。この白濁している時間をラビッドパッセ
ージ時間πに、と呼んでいるが従来の高電圧蓄積型液晶
ではπkl)に数〜数十秒を要していた。
(3) Conventional technology and problems Conventional storage type liquid crystals have a writing time of 20 to 401 na, and although some compositions can write in several ms, the temporary clouding time when transitioning to the storage state is long, and Even if the process is performed quickly, the disadvantage is that it takes a long time to display the image as a whole. This cloudy time is called the rapid passage time π, and in conventional high-voltage storage type liquid crystals, it takes several to several tens of seconds for πkl).

(4)発明の目的 本発明は、蓄積型液晶組成においてコレステリック液晶
の種類と混合比率を限定することにより、10m5以下
の高速書き込みを行い、かつ蓄積状態移行時の一時的白
濁時間を3秒以内におさえる゛液晶組成を提供するにあ
る。
(4) Purpose of the Invention The present invention enables high-speed writing of 10 m5 or less by limiting the type and mixing ratio of cholesteric liquid crystal in the storage type liquid crystal composition, and the temporary clouding time at the time of transition to the storage state is within 3 seconds. The goal is to provide a liquid crystal composition that can be controlled.

−(5)発明の構成 本発明の蓄積型液晶組成物は、正の誘電率異方性を示す
ネマティック−コレステリック混合液晶を用いた蓄積型
液晶組成物において、それぞれ下記式lの構造を持つシ
クロヘキサン系液晶、式1jaおよび/又は式nbのア
ゾキシ系液晶ならびに弐■のネdi償型コレステリック
液晶及び式1vのコレステリルノナノエイトから成り、
該補償型コレステリンク液晶と該コレステリルノナイノ
エイトとの組成比率が6〜10重量パ重量パーセントリ
、かつ補償型コレステリック液晶とコレステリルノナノ
エイトの比率が2:3以下であることを特徴と(式中R
7は炭素数1〜7の直鎮アルキル基又はυ (両式中、RLは炭素数1〜7のアルキル基又はアルコ
キシ基であり、R3は炭素数1〜7の直鎖アルキル基2
直鎖アルコキシ基、又はシアノ基である) 式II (補償型コレステリック液晶):(」二記コレ
ステリルミリスティト:コレステリルりロライドー1.
00 : 1.75重量比から成る混合物)。
-(5) Structure of the Invention The storage type liquid crystal composition of the present invention is a storage type liquid crystal composition using a nematic-cholesteric mixed liquid crystal exhibiting positive dielectric constant anisotropy. consisting of an azoxy-based liquid crystal of formula 1ja and/or formula nb, a neutralized cholesteric liquid crystal of 2) and cholesteryl nonanoate of formula 1v,
The composition ratio of the compensating cholesteric liquid crystal and the cholesteryl nonanoate is 6 to 10% by weight, and the ratio of the compensating cholesteric liquid crystal to cholesteryl nonanoate is 2:3 or less (formula Medium R
7 is a straight chain alkyl group having 1 to 7 carbon atoms or υ (In both formulas, RL is an alkyl group or alkoxy group having 1 to 7 carbon atoms, and R3 is a straight chain alkyl group having 1 to 7 carbon atoms.
Formula II (compensated cholesteric liquid crystal): (2) cholesteryl myristite: cholesteryl loride 1.
00 : 1.75 weight ratio).

式■(コレステリルノナノエイト なお、補償型コレステリック液晶とコレステリルノナノ
エイトとの組成比が10wt%より大ではπ112Pが
長くなり過ぎ、又6wt%より小ではメモリ効果が得ら
れ又補償型コレステリンク液晶とコレステリルノナノエ
イ1〜の比率が2:3より人では書き込み速度が遅くな
ってしまう。
Formula ■ (Cholesteryl Nonanoate) If the composition ratio of the compensated cholesteric liquid crystal and cholesteryl nonanoate is greater than 10 wt%, π112P becomes too long, and if it is less than 6 wt%, a memory effect is obtained, and the composition ratio of the compensated cholesteric liquid crystal and cholesteryl nonanoate is When the ratio of cholesteryl nonanoei is 1 to 2:3, the writing speed of humans becomes slower.

本発明は、蓄積型液晶組成において、補償型コレステリ
ック液晶によって混合液晶の低粘度化を図り、蓄積状態
移行時の一時的白濁時間を短くおさえ、コレステリルノ
ナノエイトによって混合液晶の示ずラセン構造のラセン
ピッチを短くしラセンを巻く力を強くすることによって
高速書き込のを行えるようにし7たものである。
The present invention aims to reduce the viscosity of the mixed liquid crystal by using the compensation type cholesteric liquid crystal in the storage type liquid crystal composition, to shorten the temporary clouding time at the time of transition to the storage state, and to reduce the helical pitch of the mixed liquid crystal by using cholesteryl nonanoate. By shortening the length and increasing the winding force of the helix, high-speed writing can be performed.

(6)発明の実施例 実施例1゜ 下記の組成で蓄積型液晶を調整し、ギヤ・7プ9μmの
セルに注入しマルチプレックス駆動を行ったところ1ラ
インあたりの書き込み時間5.8ms。
(6) Embodiments of the Invention Example 1 A storage type liquid crystal was prepared with the following composition and injected into a 9 μm cell with a gear of 7. When multiplex driving was performed, the writing time per line was 5.8 ms.

実施例2゜ 下記の組成で甜積型液晶を調整し、ギャップ9μmのセ
ルに注入しマルチプレックス駆動を行ったところlライ
ンあたりの書き込み時間6.7ms。
Example 2 When a concentrated liquid crystal was prepared with the composition shown below and injected into a cell with a gap of 9 μm and multiplex driving was performed, the writing time per 1 line was 6.7 ms.

本発明によればA4版(ライン数300本)の大型液晶
表示の一画面の書き込み力月、8秒(−ラインあたり6
m5)ででき、なおかつ蓄積状態への移行も3秒以内に
でき、大型の液晶表示を高速で駆動できる効果がある。
According to the present invention, the writing power on one screen of A4 size (300 lines) large liquid crystal display is 8 seconds (- 6 seconds per line).
m5), and the transition to the storage state can be made within 3 seconds, which has the effect of allowing large liquid crystal displays to be driven at high speed.

【図面の簡単な説明】[Brief explanation of drawings]

第1図はネマティック−コレステリック相転移を利用し
た誘電異方性が正を示す蓄積型液晶の動作原理を説明す
る図であり、図においてH,H’は光透過状態、Gは光
透過状態、F、Fo は光散乱状b+v、は駆動電圧を
それぞれ表わす。。 寥 1 口
FIG. 1 is a diagram explaining the operating principle of a storage type liquid crystal that exhibits positive dielectric anisotropy using nematic-cholesteric phase transition. In the figure, H and H' are in a light transmitting state, G is a light transmitting state, F and Fo represent the light scattering pattern b+v, and drive voltage, respectively. . 1 mouthful

Claims (1)

【特許請求の範囲】 1、 正の誘電率異方性を示すネマティック−コレステ
リック混合液晶を用いた蓄積型液晶組成物において、そ
れぞれ下記式■の構造を持つシクロヘキサン系液晶、式
11aおよび/又は式nbのアゾキシ系液晶ならびに弐
■の補償型コレステリック液晶及び式■のコレステリル
ノナノエイI・から成り、該?lli償型コ酸型コレス
テリック液晶レステリルノナノエイI・との組成比率か
6〜10重量バーセンI・であり、かつ補償型コレステ
リック液晶とコレステリルノナノエイトの比率が2:3
以下(式中Rtし1炭素数1〜7の直鎮アルキル基又は
直鎖アル」ギシ基である) υ (両式中、R2は炭素数1〜7のアルキル基又はアルコ
キシ基であり、R3は炭素数1〜7の直鎖アルキル基、
直鎖アルコキシ基、又はシアノ基である) 式II[(補償型コレステリック液晶):(上記コレス
テリルミリステイト:コレステリルクロライド−1,0
0: 1.75重量比から成る混合物) 式■ (コレステリルノナノエイト):
[Claims] 1. In a storage type liquid crystal composition using a nematic-cholesteric mixed liquid crystal exhibiting positive dielectric constant anisotropy, a cyclohexane-based liquid crystal having the structure of the following formula (2), formula 11a and/or formula It consists of an azoxy liquid crystal of nb, a compensated cholesteric liquid crystal of 2), and a cholesteryl nonanoei I of the formula 2. The composition ratio of the compensating cholesteric liquid crystal to cholesteryl nonanoate I is 6 to 10% by weight, and the ratio of the compensating cholesteric liquid crystal to cholesteryl nonanoate is 2:3.
The following (in the formula, Rt is a straight alkyl group having 1 to 7 carbon atoms or a straight chain alkoxy group) υ (In both formulas, R2 is an alkyl group or an alkoxy group having 1 to 7 carbon atoms, and R3 is a straight chain alkyl group having 1 to 7 carbon atoms,
linear alkoxy group or cyano group) Formula II [(compensated cholesteric liquid crystal): (the above cholesteryl myristate: cholesteryl chloride-1,0
0: 1.75 weight ratio) Formula ■ (Cholesteryl nonanoate):
JP15364183A 1983-08-23 1983-08-23 Liquid crystal composition Pending JPS6047093A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15364183A JPS6047093A (en) 1983-08-23 1983-08-23 Liquid crystal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15364183A JPS6047093A (en) 1983-08-23 1983-08-23 Liquid crystal composition

Publications (1)

Publication Number Publication Date
JPS6047093A true JPS6047093A (en) 1985-03-14

Family

ID=15566957

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15364183A Pending JPS6047093A (en) 1983-08-23 1983-08-23 Liquid crystal composition

Country Status (1)

Country Link
JP (1) JPS6047093A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4792213A (en) * 1985-08-12 1988-12-20 The General Electric Company, P.L.C. Thermal imaging device
EP0806466A3 (en) * 1996-05-08 1998-03-18 Chisso Corporation Liquid crystal composition, use thereof and liquid crystal display element
WO2011093734A1 (en) * 2010-01-29 2011-08-04 Braster Sp.Z O.O. Mixture of liquid-crystal compounds, system of three liquid-crystal mixtures and their use
WO2011093733A1 (en) * 2010-01-29 2011-08-04 Braster Sp. Z O.O. Liquid-crystal emulsion oil in water type and a preparation method of the liquid-crystal emulsion

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4792213A (en) * 1985-08-12 1988-12-20 The General Electric Company, P.L.C. Thermal imaging device
EP0806466A3 (en) * 1996-05-08 1998-03-18 Chisso Corporation Liquid crystal composition, use thereof and liquid crystal display element
WO2011093734A1 (en) * 2010-01-29 2011-08-04 Braster Sp.Z O.O. Mixture of liquid-crystal compounds, system of three liquid-crystal mixtures and their use
WO2011093733A1 (en) * 2010-01-29 2011-08-04 Braster Sp. Z O.O. Liquid-crystal emulsion oil in water type and a preparation method of the liquid-crystal emulsion
CN102753654A (en) * 2010-01-29 2012-10-24 布拉斯特股份有限公司 Mixture of liquid-crystal compounds, system of three liquid-crystal mixtures and their use
CN102947419A (en) * 2010-01-29 2013-02-27 布拉斯特股份有限公司 Liquid-crystal emulsion oil in water type and a preparation method of the liquid-crystal emulsion
JP2013518167A (en) * 2010-01-29 2013-05-20 ブラスター エス. エイ. Oil-in-water liquid crystal emulsion and method for preparing liquid crystal emulsion
US8574457B2 (en) 2010-01-29 2013-11-05 Braster Sa Mixture of liquid-crystal compounds, system of three liquid-crystal mixtures and their use
US8658058B2 (en) 2010-01-29 2014-02-25 Braster Sa Liquid-crystal emulsion oil in water type and a preparation method of the liquid-crystal emulsion
RU2538851C2 (en) * 2010-01-29 2015-01-10 Брастер Са Mixture of liquid crystalline compounds, system from three liquid crystalline mixtures and their application
KR101484601B1 (en) * 2010-01-29 2015-01-20 브라스터 에스에이 Mixture of liquid­crystal compounds, system of three liquid­crystal mixtures and their use
RU2542237C2 (en) * 2010-01-29 2015-02-20 Брастер Са Liquid crystalline emulsion of oil-in-water type and method of obtaining liquid crystalline emulsion

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