Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPS605631B2 - Nematic liquid crystal composition - Google Patents
[go: Go Back, main page]

JPS605631B2 - Nematic liquid crystal composition - Google Patents

Nematic liquid crystal composition

Info

Publication number
JPS605631B2
JPS605631B2 JP413375A JP413375A JPS605631B2 JP S605631 B2 JPS605631 B2 JP S605631B2 JP 413375 A JP413375 A JP 413375A JP 413375 A JP413375 A JP 413375A JP S605631 B2 JPS605631 B2 JP S605631B2
Authority
JP
Japan
Prior art keywords
liquid crystal
crystal composition
formulas
tables
nematic liquid
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.)
Expired
Application number
JP413375A
Other languages
Japanese (ja)
Other versions
JPS5174989A (en
Inventor
貞男 神戸
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.)
Suwa Seikosha KK
Original Assignee
Suwa Seikosha KK
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 Suwa Seikosha KK filed Critical Suwa Seikosha KK
Priority to JP413375A priority Critical patent/JPS605631B2/en
Priority to GB51641/75A priority patent/GB1501718A/en
Priority to US05/643,884 priority patent/US4096086A/en
Publication of JPS5174989A publication Critical patent/JPS5174989A/en
Publication of JPS605631B2 publication Critical patent/JPS605631B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Liquid Crystal Substances (AREA)

Description

【発明の詳細な説明】 本発明は新規なネマチック液晶組成物に関する。[Detailed description of the invention] The present invention relates to novel nematic liquid crystal compositions.

さらに詳しくは白色で非常に安定で、かつ温度範囲の広
いネマチツク液晶組成物に関する。近年エレクトロニク
ス等の技術の進歩により低電圧で駆動出釆、かつ安価な
表示材料が要求されている。この要求を満たす表示材料
として現在液晶が有望視されており、すでに一部の表示
体には液晶が使用されている。この有害視されている液
晶は有機化合物よりなるが、通常の化合物が固体→液体
→気体と相変化するのに対して、液晶は直接固体から液
体に変化しないでこの間に固体と液体の性質を併せ持つ
相を示す。
More specifically, the present invention relates to a nematic liquid crystal composition that is white, extremely stable, and has a wide temperature range. In recent years, advances in electronics and other technologies have created a demand for display materials that can be driven at low voltages and are inexpensive. Liquid crystals are currently seen as a promising display material that satisfies this requirement, and liquid crystals are already being used in some displays. Liquid crystals, which are considered harmful, are made of organic compounds, but while ordinary compounds undergo a phase change from solid to liquid to gas, liquid crystals do not directly change from solid to liquid, but instead have the properties of solid and liquid. Indicates the phase that it has.

液晶はこの相の分子配向の違いによりスメクチック液晶
、ネマチツク液晶、コレステリック液晶に分けられる。
現在表示材料として使用されている液晶はネマチック液
晶であり、このネマチツク液晶を使用した表示体の表示
方式には光散乱方式と、電界効果型方式の二種類がある
Liquid crystals can be divided into smectic liquid crystals, nematic liquid crystals, and cholesteric liquid crystals depending on the molecular orientation of this phase.
The liquid crystal currently used as a display material is a nematic liquid crystal, and there are two types of display methods for display bodies using this nematic liquid crystal: a light scattering method and a field effect method.

本発明は電界効果型方式の表示体に用いられるネマチッ
ク液晶組成物についてなされた。
The present invention was made regarding a nematic liquid crystal composition used in a field effect type display.

さて液晶は表示材料として非常に有望であるが、次のよ
うな欠点や改良点が従来の液晶材料には残されていた。
Although liquid crystals are very promising as display materials, conventional liquid crystal materials still have the following drawbacks and points for improvement.

1 有機化合物であることからくる液晶の不安定性。と
くに従来の液晶は分子中央にシッフ塩基を有する化合物
(以下シツフ液晶と略記する)であったので、水分に対
して非常に敏感であり、劣化しやすく、とり扱いにくか
った。2 比較的安定な液晶としてアゾキシ化合物系の
液晶(以下アゾキシ液晶と略記する)があるが、このア
ゾキシ液晶は可視領域の光を吸収するため紫外線よりの
可視光によっても劣化する欠点がある。
1. Instability of liquid crystals due to being an organic compound. In particular, conventional liquid crystals are compounds having a Schiff base at the center of the molecule (hereinafter abbreviated as Schiff liquid crystals), and are therefore extremely sensitive to moisture, easily deteriorate, and difficult to handle. 2.A relatively stable liquid crystal is an azoxy compound-based liquid crystal (hereinafter abbreviated as azoxy liquid crystal), but since this azoxy liquid crystal absorbs light in the visible region, it has the disadvantage of being degraded by visible light such as ultraviolet rays.

この欠点を取り除くため有色のフィルターで表示部を保
護するような事も考えられたが、この方法だと表示部全
体が特定の色に着色し、暗くなり表示能力がおちる欠点
があった。3 前記1、2の欠点を有しない液晶として
白色で非常に安定なェステル系化合物の液晶(以下ェス
テル液晶と略記する)があるが、従来のェステル液晶は
温度範囲が非常に限定されており、使用面で制約をうけ
ていた。
In order to eliminate this drawback, it was considered to protect the display section with a colored filter, but this method had the drawback that the entire display section was colored in a specific color, making it dark and reducing the display ability. 3. As a liquid crystal that does not have the above disadvantages 1 and 2, there is a white and very stable liquid crystal of an ester compound (hereinafter abbreviated as ester liquid crystal), but the conventional ester liquid crystal has a very limited temperature range, There were restrictions on its use.

例えば一般式(Rは直鎖アルキル基)で表わされる液晶
の数種類を混合した液晶組成物が考えられた。
For example, a liquid crystal composition in which several types of liquid crystals represented by the general formula (R is a linear alkyl group) is mixed has been considered.

しかしこの液晶組成物は、液晶でなくなる上限の点(ク
リヤーポイント以下C.Pと略記する)が5000以下
とCPが低すぎる欠点を有していた。
However, this liquid crystal composition had the disadvantage that the upper limit point at which it ceases to be a liquid crystal (hereinafter referred to as clear point, abbreviated as CP) is 5000 or less, which is too low.

又、前記ェステル液晶に一般式が(R.R′は直鎖ア ルキル基を意味する)で表わされる液晶を混合した液晶
組成物も考えられたが、この液晶組成物もCPが50q
o以下となり満足出来るものでなかった。
Also, a liquid crystal composition was considered in which a liquid crystal represented by the general formula (R.R' means a linear alkyl group) was mixed with the above-mentioned Ester liquid crystal, but this liquid crystal composition also had a CP of 50q.
o or less, which was not satisfactory.

CPを上げる目的で、一般式が (R.R′は直 鎖アルキル基を意味する)で表わされる液晶を前記ェス
テル液晶に混合したェ ステル液晶組成物が考えられた。
In order to increase the CP, an ester liquid crystal composition was considered in which a liquid crystal represented by the general formula (R.R' means a straight-chain alkyl group) was mixed with the ester liquid crystal.

この方法によりCPをあげることはできたが、しかし寿
命試験をしたところ、分子末端のェステル結合に劣化が
おこり電界効果型表示体の致命傷ともいうべき分子配向
に乱れを生じ、表示不可能となった。
Although it was possible to increase the CP using this method, a life test revealed that the ester bond at the end of the molecule deteriorated, causing disturbance in the molecular orientation, which is a fatal flaw for field-effect displays, and rendering it impossible to display. Ta.

又、アゾキシ液晶やシッフ液晶が過冷却状態を長時間保
持出来たのに対して従来のェステル液晶は長時間の保持
が出釆なかった。
Further, whereas azoxy liquid crystals and Schiff liquid crystals can maintain a supercooled state for a long time, conventional Estel liquid crystals cannot maintain a supercooled state for a long time.

このため製品を作っても寒冷地での使用は困難であった
。本発明は、表1に示す7種のェステル液晶を混合する
ことにより、前記1、2で述べた欠点はもとより、従来
のェステル液晶が有していた前記3で述べた欠点をも解
決したものである。
For this reason, even if products were manufactured, it was difficult to use them in cold regions. The present invention solves not only the drawbacks mentioned in 1 and 2 above, but also the drawbacks mentioned in 3 above of the conventional Ester liquid crystal by mixing the seven types of Estel liquid crystals shown in Table 1. It is.

本発明で用いたェステル液晶の特性を表1に示す。Table 1 shows the properties of the Estel liquid crystal used in the present invention.

表 1 表においてC、N、1はそれぞれ結晶状態、ネマチック
液晶状態、等方性液体状態を示す。
Table 1 In the table, C, N, and 1 indicate a crystalline state, a nematic liquid crystal state, and an isotropic liquid state, respectively.

以下の表においても同様である。表1にあるような化合
物を用いて調合した本発明のネマチック液晶組成物の成
分と、その割合と、その特性の一例を実施例1に示す。
The same applies to the table below. Example 1 shows the components of the nematic liquid crystal composition of the present invention prepared using the compounds shown in Table 1, their proportions, and an example of their properties.

実施例1 実施例1からわかるように本発明の液晶組成物のmpは
従来のェステル系液晶の組成物より数度低く、CPは5
000を充分確保していることがわかる。
Example 1 As can be seen from Example 1, the mp of the liquid crystal composition of the present invention is several degrees lower than that of the conventional ester-based liquid crystal composition, and the CP is 5.
It can be seen that 000 is sufficiently secured.

又過冷却の試験においても一1oo○で1虫時間結晶化
しなかった。このように本発明の液晶組成物は従来の液
晶と比較して温度特性の面はもとより、安定性の面でも
、表示能力の面でもすぐれており、製品とした場合寒冷
地でも充分使用に耐えるものを提供することが出釆る。
このような特性を有す液晶組成物は電卓、腕時計等の表
示部はもとより種々の機器の表示部にも応用出来るもの
である。
In addition, in the supercooling test, crystallization did not occur for 1 hour at 100°. As described above, the liquid crystal composition of the present invention is superior in terms of temperature characteristics, stability, and display ability compared to conventional liquid crystals, and when made into a product, it can withstand use even in cold regions. It is possible to provide something.
A liquid crystal composition having such characteristics can be applied not only to the display parts of calculators, wristwatches, etc., but also to the display parts of various devices.

尚、本発明の液晶組成物を用いた腕時計を試作したが寿
命、コントラスト等、種々の点に関しても問題となるよ
うなところがなかった。
A prototype wristwatch was produced using the liquid crystal composition of the present invention, but there were no problems with respect to various aspects such as lifespan and contrast.

Claims (1)

【特許請求の範囲】 1 構造式が ▲数式、化学式、表等があります▼ で表わさ れる化合物、 ▲数式、化学式、表等があります▼ で表わさ れる化合物、 ▲数式、化学式、表等があります▼ で表わさ れる化合物、 ▲数式、化学式、表等があります▼ で表わさ れる化合物、 ▲数式、化学式、表等があります▼ で表わさ れる化合物、 ▲数式、化学式、表等があります▼ で表わされる化合物および ▲数式、化学式、表等があります▼ で表わされる化合物からなることを特徴とするネマチツ
ク液晶組成物。
[Claims] 1. A compound whose structural formula is ▲There are mathematical formulas, chemical formulas, tables, etc.▼ ▲There are mathematical formulas, chemical formulas, tables, etc.▼ Compounds whose structural formula is represented by ▲There are mathematical formulas, chemical formulas, tables, etc.▼ Compounds represented by ▲ There are mathematical formulas, chemical formulas, tables, etc.▼ Compounds represented by ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ Compounds represented by ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ Compounds represented by and ▲There are mathematical formulas, chemical formulas, tables, etc.▼ A nematic liquid crystal composition characterized by consisting of a compound represented by the following.
JP413375A 1974-12-23 1974-12-25 Nematic liquid crystal composition Expired JPS605631B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP413375A JPS605631B2 (en) 1974-12-25 1974-12-25 Nematic liquid crystal composition
GB51641/75A GB1501718A (en) 1974-12-23 1975-12-17 Nematic liquid crystal material
US05/643,884 US4096086A (en) 1974-12-23 1975-12-23 Nematic liquid crystal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP413375A JPS605631B2 (en) 1974-12-25 1974-12-25 Nematic liquid crystal composition

Publications (2)

Publication Number Publication Date
JPS5174989A JPS5174989A (en) 1976-06-29
JPS605631B2 true JPS605631B2 (en) 1985-02-13

Family

ID=11576270

Family Applications (1)

Application Number Title Priority Date Filing Date
JP413375A Expired JPS605631B2 (en) 1974-12-23 1974-12-25 Nematic liquid crystal composition

Country Status (1)

Country Link
JP (1) JPS605631B2 (en)

Also Published As

Publication number Publication date
JPS5174989A (en) 1976-06-29

Similar Documents

Publication Publication Date Title
AU589597B2 (en) Smectic a liquid crystal compositions
US4469618A (en) Liquid crystal mixture
JPS605631B2 (en) Nematic liquid crystal composition
US4003844A (en) Liquid crystal devices
JPS604858B2 (en) Nematic liquid crystal composition
JPH03271242A (en) Cyclopropylallylbenzenes
JPS604857B2 (en) Nematic liquid crystal composition
JPH0243283A (en) Ferroelectric liquid crystal composition
US4203862A (en) Liquid crystal composition
JP3531696B2 (en) Liquid crystal composition and liquid crystal display device
JPS5945019B2 (en) Nematic liquid crystal composition
JPS5945020B2 (en) Nematic liquid crystal composition
JPS604860B2 (en) Nematic liquid crystal composition
JPS6146513B2 (en)
JPS5940867B2 (en) Nematic liquid crystal composition
JPS59149975A (en) Liquid crystal composition
JPH0726101B2 (en) Ferroelectric liquid crystal composition and optical switching element
JP2001226675A (en) Liquid crystal composition
JPS6048557B2 (en) Nematic liquid crystal composition
JPS604859B2 (en) Nematic liquid crystal composition
JPS6050234B2 (en) Nematic liquid crystal composition
JPS5943504B2 (en) liquid crystal mixture
JPS6048560B2 (en) Nematic liquid crystal composition
JPH01254794A (en) Liquid crystal composition
JPH0726100B2 (en) Liquid crystal composition and liquid crystal display device