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JPS591586A - Liquid crystal composition - Google Patents

Liquid crystal composition

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Publication number
JPS591586A
JPS591586A JP10934182A JP10934182A JPS591586A JP S591586 A JPS591586 A JP S591586A JP 10934182 A JP10934182 A JP 10934182A JP 10934182 A JP10934182 A JP 10934182A JP S591586 A JPS591586 A JP S591586A
Authority
JP
Japan
Prior art keywords
liquid crystal
crystal composition
chain alkyl
carbon atoms
alkyl group
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
JP10934182A
Other languages
Japanese (ja)
Inventor
Osamu Yamazaki
修 山崎
Shuhei Yamamoto
修平 山本
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.)
Seiko Instruments Inc
Original Assignee
Seiko Instruments Inc
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 Seiko Instruments Inc filed Critical Seiko Instruments Inc
Priority to JP10934182A priority Critical patent/JPS591586A/en
Publication of JPS591586A publication Critical patent/JPS591586A/en
Pending legal-status Critical Current

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  • Liquid Crystal Substances (AREA)

Abstract

PURPOSE:To provide a liquid crystal composition containing specified liquid crystal compds., which has a wide liquid crystal temperature range, is less dependent on temperature, shows good response and is suitable for high-level time- division drive. CONSTITUTION:The liquid crystal composition contains (A) 10-40% m-dioxane liquid crystal compd. of formula I (where R1 is 3-5C straight-chain alkyl) (e.g., 2-p-cyanophenyl-5-n-propyl-1,3-m-dioxane), (B) 10-40% fluorocyclohexanecarboxylic acid ester liquid crystal compd. of formula II (where R2 is 3-7 C straight-chain alkyl) (e.g. 4-fluorophenyl trans-4'-n-pentylcyclohexanecarboxylic acid ester), (C) 2-20% PCH liquid crystal compd. of formula III (where R3 and R4 are 2-6C alkyl) having negative dielectric anisotropy [e.g. 4- (trans-4-propylhexyl)ethxoybenzene] and (D) an optically active substance (e.g. p-isopentyl-p'- cyano-biphenyl).

Description

【発明の詳細な説明】 本発明は、時分割駆動用液晶組成物に関するものである
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a liquid crystal composition for time-division driving.

対問する1板の透明電極を有するガラス基板間に、正の
ネマチック液晶を平行配向させ、表示画素に電圧を印加
除去を行なう事により画g1表示を行なう液晶表示体は
、いわゆる電界効果屋液晶表示装置と呼ばれ、従来より
電卓、時計、ゲーム、計測機器、事務機器々どのデスプ
レー用として広範囲に使用されているが、最近の市場動
向として、より多くの情報表示量が塔載できる液晶表示
体の要求が高まっている。この様な要求に対応した駆動
方式の一つに時分割駆動方式(マルチプレクス、駆動)
がおり、現在、高時分割駆動の液晶表示装置も市場に出
される様になってきた。
A liquid crystal display that displays an image G1 by aligning positive nematic liquid crystal in parallel between two glass substrates with transparent electrodes and applying and removing voltage to display pixels is a so-called field effect liquid crystal display. It is called a display device and has been widely used for displays such as calculators, clocks, games, measuring instruments, office equipment, etc., but recent market trends are such that liquid crystal displays can display more information. Demands on the body are increasing. One of the drive methods that meets these requirements is the time-division drive method (multiplex, drive).
Nowadays, liquid crystal display devices with high time-division driving are coming onto the market.

それにともない、高時分割駆動に適した液晶組゛成物の
出現が望まれるわけであるが、その為に要求される特性
としては、 (1)電圧輝度特性が急峻である事 (り低粘度である事 (■温度依存性が小さい事 (4)広温度範囲である事 などの特性をもった温晶である事が必要である。
Accordingly, the emergence of a liquid crystal composition suitable for high-time division driving is desired, and the characteristics required for this are (1) steep voltage-luminance characteristics (low viscosity, low viscosity, etc.); It needs to be a warm crystal with characteristics such as (■) low temperature dependence (4) wide temperature range.

さらに、駆動電圧も低電圧化される傾向にあり液晶組成
物としては低電圧輝度特性を有した液晶組成物の必要性
も生じてきている。
Furthermore, as driving voltages tend to be lowered, there is also a need for liquid crystal compositions having low voltage brightness characteristics.

とかなシ急峻性が悪くなり、多分割用液晶としては実用
に適さない、また応登速度に関しても、従来のビフェニ
ル。エステル系は粘度が比較的高い為、応答速度は一般
に遅いという問題点があった本発明は、上記の様な問題
点を除去する為になされたものであり、電圧輝度特性の
急峻性、応答性に優れた、さらに低電圧化しても急峻性
、応答性の優れた液晶組成物を提供する事を目的とした
ものである。即ち、本液晶組成物の特徴は、メタジオキ
サン系液晶化合物(Rs −CgX)ON )とフルオ
ロシクロヘキサンカルボン酸エステル系液晶化合物(R
t −@rO−o−o−Ir) ト負’り n [異方
性’x有するPOH系(Rs−位>0−R4)と光学活
性物質を主体としたものであり、それに各種品質特性に
合せて他の液晶化合物を混合する裏により、電圧輝度特
性、応答性の優れた液晶組成物が得られる。さらに上記
液晶組成物を主体としたものであれば急峻性、応答性を
そこなわずにかなりの低電圧化も計れる点にある。
It has poor steepness, making it unsuitable for practical use as a multi-segment liquid crystal, and the response speed is also lower than that of conventional biphenyl. The ester type has a relatively high viscosity, so the response speed is generally slow.The present invention was made to eliminate the above-mentioned problems. The purpose of this invention is to provide a liquid crystal composition that has excellent properties, and also has excellent sharpness and responsiveness even when the voltage is lowered. That is, the characteristics of the present liquid crystal composition include a metadioxane-based liquid crystal compound (Rs-CgX)ON) and a fluorocyclohexanecarboxylic acid ester-based liquid crystal compound (Rs-CgX)ON).
t -@rO-o-o-Ir) Negative n By mixing other liquid crystal compounds accordingly, a liquid crystal composition with excellent voltage-luminance characteristics and responsiveness can be obtained. Furthermore, if the composition is based on the above-mentioned liquid crystal composition, it is possible to achieve a considerably lower voltage without impairing steepness or response.

以下実施例に従い本発明を説明する。第−表に実施例の
液晶組成比金示す。
The present invention will be explained below with reference to Examples. Table 1 shows the liquid crystal composition ratios of Examples.

実施例1は、2−P−シアノフェニル−5−yaプロヒ
ル−1,3−メタジオキサン(以下0D−3、lj、)
 及び2−P−シアノフェニル−5−n−ブチル−1,
3−メタジオキサンC以下0D−4,!:略す。) 及
び、4−フルオロフェニル−トランス−4’−nペンチ
ルシクロヘキサンカルボン酸エステルC以下5HE]Z
と略す。〕及び、〕4−フルオロフェニルートランス4
1−sヘプチルシクロヘキサンカルボン酸エステル(以
下7 HPZと略す。)及び、4−(トランス−4−プ
ロ5− ビルシクロヘキシル)−エトキシベンゼン(以下3Pθ
2と略す。)及び、4エチル安息香酸−41−シアノフ
ェニルエステル(以下2”0と略ス。
Example 1 is 2-P-cyanophenyl-5-ya proyl-1,3-metadioxane (hereinafter referred to as 0D-3, lj)
and 2-P-cyanophenyl-5-n-butyl-1,
3-metadioxane C or less 0D-4,! :Omitted. ) and 4-fluorophenyl-trans-4'-n pentylcyclohexanecarboxylic acid ester C or less 5HE]Z
It is abbreviated as ] and] 4-fluorophenyltrans 4
1-s heptylcyclohexanecarboxylic acid ester (hereinafter abbreviated as 7HPZ) and 4-(trans-4-pro5-bicyclohexyl)-ethoxybenzene (hereinafter abbreviated as 3Pθ)
Abbreviated as 2. ) and 4-ethylbenzoic acid-41-cyanophenyl ester (hereinafter abbreviated as 2"0).

)及び、4−nブチル安息香酸−4′−シアノフェニル
エステル(以下4KOと略す。)及び1.4−n−ブチ
ルシクロヘキサンカルボン酸−41−エトキシフェニル
エステル(以下4HBθ2と略す。)及ヒ4− x−プ
ロピルシクロヘキサンカルボン酸−41−エトキシフェ
ニルエステル(以下3HKθ2と略す、)及びP−3−
ペンチルシクロヘキサン−p+−シアノビフェニル(以
下5 HBOと略す。)及びP−3−ベンチルーア1−
シ了ツターフェニルC以下T 15と略す。〕及び〕P
−ルーペンチルシクへキチン−P’−B−プロピルシク
ロヘキサンビフェニル(以下0BO−53と略す。)及
びP−イソベンチルーp+シアノビフェニル(以下OB
 −15と略す。)の液晶を混合した液晶組成物。
), 4-n-butylbenzoic acid-4'-cyanophenyl ester (hereinafter abbreviated as 4KO), 1.4-n-butylcyclohexanecarboxylic acid-41-ethoxyphenyl ester (hereinafter abbreviated as 4HBθ2), and H4 - x-propylcyclohexanecarboxylic acid-41-ethoxyphenyl ester (hereinafter abbreviated as 3HKθ2) and P-3-
Pentylcyclohexane-p+-cyanobiphenyl (hereinafter abbreviated as 5 HBO) and P-3-ventilur 1-
It is abbreviated as T15 below. ]and]P
-Lupentylcyclohexachitin-P'-B-propylcyclohexane biphenyl (hereinafter abbreviated as 0BO-53) and P-isobenthyl p+cyanobiphenyl (hereinafter OB
It is abbreviated as -15. ) liquid crystal composition.

実施例2は、0D−3,0D−4,5H]l[iZ。Example 2 is 0D-3,0D-4,5H]l[iZ.

7HEZ、3Pθ2.4HEθ2.3HElθ2、6− 4mo、5HBO,T15.0B−15の液晶を混合し
た液晶組成物。
A liquid crystal composition in which liquid crystals of 7HEZ, 3Pθ2.4HEθ2.3HElθ2, 6-4mo, 5HBO, and T15.0B-15 are mixed.

11人 下 iマロ − 7一 以上列記した混合液晶の組成比と液晶温度範囲を表−1
に、父上記液晶Mi底物を透過型液晶セル(セル厚〜1
0μ?+1.、千行配同処理、ツイスト角は答速度(0
℃と25℃)を第2表に示す。
11 people Lower i Maro - Table 1 shows the composition ratio and liquid crystal temperature range of the mixed liquid crystals listed above.
Then, the above liquid crystal Mi base material was converted into a transmission type liquid crystal cell (cell thickness ~1
0 μ? +1. , 1,000-line alignment process, the twist angle is the answer speed (0
℃ and 25℃) are shown in Table 2.

−)・又千 敞 自 − く第2表〉 (0注1) Vth、 V8cLtは電圧無印加時の透
過率がそれぞれ10%、901f化する時の実効電圧で
ある(注2)p値=(■8αt −v t5 /V t
h(注3)γ値= (V 50%−V th) /V 
th第−表、第二表より明らかな様に、本発明の液晶組
成物によれば、液晶温度範囲が広く、温度依存性の小さ
い、かつ急峻性の優れた特性が得られる。tた、応答速
度に関しても従来のビフェニル系に比べて優るとも劣ら
ない特性を示している。
Table 2〉 (Note 1) Vth and V8cLt are the effective voltages when the transmittance becomes 10% and 901f when no voltage is applied, respectively (Note 2) p value = (■8αt −v t5 /V t
h (Note 3) γ value = (V 50% - V th) /V
As is clear from Tables 1 and 2, the liquid crystal composition of the present invention has a wide liquid crystal temperature range, low temperature dependence, and excellent steepness. Furthermore, in terms of response speed, it exhibits characteristics that are as good as, if not superior to, conventional biphenyl-based products.

従って、高時分割用液晶として従来のビフェニル。エス
テル系液よりも著しく改善された液晶組成物であると言
う事ができる。
Therefore, conventional biphenyl as a liquid crystal for high time division. It can be said that the liquid crystal composition is significantly improved over ester-based liquids.

以上 出願人 株式会社第二精工★ 代理人 弁理士最上  務 11−that's all Applicant: Daini Seiko Co., Ltd.★ Agent: Patent Attorney Mogami 11-

Claims (1)

【特許請求の範囲】 (1)  一般式が  R1−ぐ:)−e−ON  (
但し、R8は炭素数3〜5の直鎖アルキル基を示す、)
で表わされる液晶化合物全10%〜40%含有し、かっ
け炭素数3〜7の直鎖アルキル基を示す。)で表わされ
る液晶化合物全10%〜40%含有し、かつ一般式が、
Rs −訃0−R+   (但し、RIsR4は炭素数
2〜6の直鎖アルキル基を示す。〕で表わされる液晶化
合物を2〜20q6含有し、かつ光学活性物負ヲ含有し
ている液晶組成物。 し、R6は炭素数2〜6の直鎖アルキル基を示す。)で
表わされる液晶化合物を含有する特許請求の範囲第1項
記載の液晶組成物。 但し、Ra*R7は炭素数2〜4の直鎖アルキル基を示
す。)で表わされる液晶化合物を含有する特許請求の範
囲第1項又は第2項記載の液晶組成物。 (4)  一般式が  R6−〔昏ON   (但し、
R8は炭素数3〜7の直鎖アルキル基を示す。〕で表わ
される液晶化合物を含有する特許請求の範囲第1項第2
項又は3項記載の液晶組成物。 (5)一般式が  R9−◎梨トON(但し、Roは炭
素数3〜6の直鎖アルキル基を示す。)で表わされる液
晶化合物を含有する特許請求の範囲第1項、2項又は3
項記載の液晶組成物。 (6)一般式が  RIO−軟鴬亭R11(但し、Rl
Gは炭素数3〜5の直鎖アルキル基を示す。)で表わさ
れる液晶化合物を含有する特許請求の範囲第1項、2項
、3項又は4項記載の液晶組成物(ことで、−〇−はト
ランス型シクロヘキサンを示す。〕
[Claims] (1) The general formula is R1-g:)-e-ON (
However, R8 represents a straight chain alkyl group having 3 to 5 carbon atoms.)
It contains a total of 10% to 40% of the liquid crystal compound represented by the formula, and represents a linear alkyl group having 3 to 7 carbon atoms. ) contains a total of 10% to 40% of the liquid crystal compound represented by
A liquid crystal composition containing 2 to 20q6 liquid crystal compounds represented by Rs -0-R+ (where RIsR4 represents a straight-chain alkyl group having 2 to 6 carbon atoms) and also contains an optically active substance. 2. The liquid crystal composition according to claim 1, which contains a liquid crystal compound represented by the formula (wherein R6 represents a straight-chain alkyl group having 2 to 6 carbon atoms). However, Ra*R7 represents a straight chain alkyl group having 2 to 4 carbon atoms. ) The liquid crystal composition according to claim 1 or 2, which contains a liquid crystal compound represented by: (4) The general formula is R6-[koON (however,
R8 represents a straight chain alkyl group having 3 to 7 carbon atoms. ] Claim 1, item 2 containing a liquid crystal compound represented by
The liquid crystal composition according to item 1 or 3. (5) Claims 1, 2, or 3
The liquid crystal composition described in . (6) The general formula is RIO-Softhoutei R11 (however, Rl
G represents a straight chain alkyl group having 3 to 5 carbon atoms. ) The liquid crystal composition according to claim 1, 2, 3 or 4, which contains a liquid crystal compound represented by (where -0- represents trans-cyclohexane).
JP10934182A 1982-06-25 1982-06-25 Liquid crystal composition Pending JPS591586A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10934182A JPS591586A (en) 1982-06-25 1982-06-25 Liquid crystal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10934182A JPS591586A (en) 1982-06-25 1982-06-25 Liquid crystal composition

Publications (1)

Publication Number Publication Date
JPS591586A true JPS591586A (en) 1984-01-06

Family

ID=14507764

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10934182A Pending JPS591586A (en) 1982-06-25 1982-06-25 Liquid crystal composition

Country Status (1)

Country Link
JP (1) JPS591586A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4737312A (en) * 1984-10-17 1988-04-12 Merck Patent Gesellschaft Mit Beschrankter Haftung Liquid crystal composition
US4846999A (en) * 1984-07-09 1989-07-11 Casio Computer Co., Ltd. Liquid crystal composition

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5668636A (en) * 1979-11-07 1981-06-09 Dainippon Ink & Chem Inc Phenyl cyclohexane derivative
JPS56100886A (en) * 1980-01-18 1981-08-13 Chisso Corp Liquid crystal composition
JPS56149486A (en) * 1980-04-21 1981-11-19 Chisso Corp Nematic liquid crystal composition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5668636A (en) * 1979-11-07 1981-06-09 Dainippon Ink & Chem Inc Phenyl cyclohexane derivative
JPS56100886A (en) * 1980-01-18 1981-08-13 Chisso Corp Liquid crystal composition
JPS56149486A (en) * 1980-04-21 1981-11-19 Chisso Corp Nematic liquid crystal composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4846999A (en) * 1984-07-09 1989-07-11 Casio Computer Co., Ltd. Liquid crystal composition
US4737312A (en) * 1984-10-17 1988-04-12 Merck Patent Gesellschaft Mit Beschrankter Haftung Liquid crystal composition

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