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JPS5945020B2 - Nematic liquid crystal composition - Google Patents
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JPS5945020B2 - Nematic liquid crystal composition - Google Patents

Nematic liquid crystal composition

Info

Publication number
JPS5945020B2
JPS5945020B2 JP2485476A JP2485476A JPS5945020B2 JP S5945020 B2 JPS5945020 B2 JP S5945020B2 JP 2485476 A JP2485476 A JP 2485476A JP 2485476 A JP2485476 A JP 2485476A JP S5945020 B2 JPS5945020 B2 JP S5945020B2
Authority
JP
Japan
Prior art keywords
liquid crystal
crystal composition
ester
nematic liquid
liquid crystals
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
JP2485476A
Other languages
Japanese (ja)
Other versions
JPS52107286A (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 JP2485476A priority Critical patent/JPS5945020B2/en
Publication of JPS52107286A publication Critical patent/JPS52107286A/en
Publication of JPS5945020B2 publication Critical patent/JPS5945020B2/en
Expired legal-status Critical Current

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  • Liquid Crystal Substances (AREA)

Description

【発明の詳細な説明】 不発明は新規なネマチツク液晶組成物に係わり、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。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel nematic liquid crystal composition, and more particularly to a nematic liquid crystal composition that is white, very stable, and has a wide temperature range.

近年エレクトロニクス技術等の進歩により低電圧で駆動
でき、かつ安価な表示材料が要求されている。
In recent years, advances in electronics technology have created a demand for inexpensive display materials that can be driven at low voltages.

この要求を満たす表示材料として、現在液晶が注目され
ており、既に一部の商品には液晶が使用されている。こ
の注目されている液晶は有機化合物よりなるが、一般の
有機化合物が結晶→液体と相変化するのに対して液晶は
結晶から直接液体に変化しないで、この間に液体の持つ
流動性と結晶の持つ複屈折性を併せ持つ相を示す。この
ような性質を有す液晶は液晶分子の配向の違いによリネ
マチツク液晶、スメクチツタ液晶、コレステリツク液晶
に分けられる。現在表示材料として主に使用されている
液晶はネマチツク液晶であり、このネマチツク液晶を用
いた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 are currently attracting attention as a display material that satisfies this requirement, and liquid crystals are already being used in some products. The liquid crystals that are attracting attention are made of organic compounds, but while ordinary organic compounds undergo a phase change from crystal to liquid, liquid crystals do not directly change from crystal to liquid; Indicates a phase that also has birefringence. Liquid crystals having such properties are classified into linematic liquid crystals, smectic liquid crystals, and cholesteric liquid crystals, depending on the orientation of liquid crystal molecules. The liquid crystal currently mainly used as a display material is a nematic liquid crystal, and there are two types of display methods using this nematic liquid crystal: a light scattering method and a field effect method.

本発明のネマチツク液晶組成物は電界効果型方式に用い
られる液晶である。さて液晶は表示材料として非常に有
望であるが、液晶が表示材料として用いられるためには
次のようなことが要求される。
The nematic liquid crystal composition of the present invention is a liquid crystal used in a field effect type system. Now, liquid crystal is very promising as a display material, but the following requirements are required for liquid crystal to be used as a display material.

1.液晶が化学的に安定であり、熱、光、酸素等により
分解劣化しないこと。
1. Liquid crystals must be chemically stable and will not decompose or deteriorate due to heat, light, oxygen, etc.

2.液晶温度範囲が広いこと。2. Wide liquid crystal temperature range.

このようなことが液晶材料には少なくとも要求されるが
、従来の液晶材料には次のような欠点や改良しなけれは
ならない点があつた。
Although this is at least required for liquid crystal materials, conventional liquid crystal materials have the following drawbacks and points that need to be improved.

*].従来の液晶は主に分子中央にシツフ
塩基を有する液晶であつた(以下シツフ液晶と略記する
)。しかし、シツフ液晶は水分の影響を受けやすいので
、取り扱いやシールドが難しかつた。2 比較的安定な
液晶としてアゾキシ化合物系の液晶がある(以下アゾキ
シ液晶と略記する)。
*]. Conventional liquid crystals mainly have a Schiff base at the center of the molecule (hereinafter abbreviated as Schiff liquid crystal). However, Schizophrenic liquid crystals are easily affected by moisture, making them difficult to handle and shield. 2. Azoxy compound-based liquid crystals are relatively stable liquid crystals (hereinafter abbreviated as azoxy liquid crystals).

しかしこの液晶は可視領域の光を吸収するため、紫外線
よりの可視光によつても劣化する欠点がある。この欠点
を除去する方法としては有色フイルタ一で表示部を保護
する必要がある。しかしこの方法では表示部全体が特定
の色に着色し、暗くなり、表示能力がおちるという欠点
がある。3.上記1、2で述べた欠点を有しない液晶と
して白色で非常に安定な分子中央にエステル結合を有す
る液晶がある(以下エステル液晶と略記する)。
However, since this liquid crystal absorbs light in the visible region, it has the disadvantage that it deteriorates even when exposed to visible light such as ultraviolet rays. In order to eliminate this drawback, it is necessary to protect the display section with a colored filter. However, this method has the disadvantage that the entire display section is colored in a specific color, becomes dark, and the display performance deteriorates. 3. As a liquid crystal that does not have the drawbacks mentioned in 1 and 2 above, there is a white and very stable liquid crystal having an ester bond in the center of the molecule (hereinafter abbreviated as ester liquid crystal).

しかしエステル液晶は液晶温度範囲が充分に確保できな
いため、従来の表示体には使われなかつた。またこの他
に応答速度が遅い欠点があつた。本発明はシツフ液晶や
アゾキシ液晶が有する1、2で述べた欠点を有しないエ
ステル液晶を用い、従来のエステル液晶が有していた温
度範囲がせまく、応答速度が遅いという欠点を改良する
ためになされた。
However, ester liquid crystals have not been used in conventional displays because a sufficient liquid crystal temperature range cannot be secured. Another drawback was that the response speed was slow. The present invention uses an ester liquid crystal that does not have the disadvantages mentioned in 1 and 2 of Schiff liquid crystals and azoxy liquid crystals, and improves the disadvantages of conventional ester liquid crystals such as narrow temperature range and slow response speed. It was done.

本発明のネマチツク液晶組成物は次のような四種類の液
晶を少なくとも含む液晶組成物である。
The nematic liquid crystal composition of the present invention is a liquid crystal composition containing at least the following four types of liquid crystals.

上記の液晶はそれぞれ次のような性質を有す液晶である
。4−n−アルキル安息香酸−4′−シアノフエニルエ
ステルは誘電異方性が正の液晶であり、電界効果型液晶
にとつては必要不可欠な液晶である。
The above liquid crystals each have the following properties. 4-n-alkylbenzoic acid-4'-cyanophenyl ester is a liquid crystal with positive dielectric anisotropy, and is an essential liquid crystal for field effect liquid crystals.

4−n−アルキル安息香酸−41−n−アルコキシフエ
ニルエステルは液晶温度範囲がせまいが、融点の低い液
晶であり、ネマチツク液晶組成物の融点を下げるために
必要である。
4-n-alkylbenzoic acid-41-n-alkoxyphenyl ester is a liquid crystal with a narrow liquid crystal temperature range but a low melting point, and is necessary to lower the melting point of the nematic liquid crystal composition.

4−n−アルコキシ安息香酸−4!−n−アルキルフエ
ニルエステルは液晶表示体の応答速度を速める性質があ
る。
4-n-alkoxybenzoic acid-4! -n-alkyl phenyl ester has the property of increasing the response speed of a liquid crystal display.

4一(4−n−アルキルベンゾイルオキシ)一安息香酸
−27−クロル−47−シアノフエニルエステルは融点
は高いが液晶温度範囲が広いのでネマチツク液晶組成物
の温度範囲を広げるために必要である。
4-(4-n-alkylbenzoyloxy)monobenzoic acid-27-chloro-47-cyanophenyl ester has a high melting point but a wide liquid crystal temperature range, so it is necessary to widen the temperature range of nematic liquid crystal compositions. .

上記四種類の液晶の代表的特性を表1に示す。Typical characteristics of the four types of liquid crystals mentioned above are shown in Table 1.

このような四種類の液晶を混合することにより非常に良
い特性が得られた。以下実施例により調合例を述べる。
Very good characteristics were obtained by mixing these four types of liquid crystals. Preparation examples will be described below with reference to Examples.

実施例 1 実施例 2 実施例1の4−n−ブチル安息香酸−4″−シアノフエ
ニルエステルの代わりに4−n−ヘブチル一4′−シア
ノビフエニールを混合したネマチツク液晶組成物。
Example 1 Example 2 A nematic liquid crystal composition in which 4-n-hebutyl-4'-cyanobiphenyl was mixed in place of the 4-n-butylbenzoic acid-4''-cyanophenyl ester of Example 1.

この液晶組成物の液晶温度範囲は5〜60℃である。実
施例 3 実施例1の液晶組成物に5重量パーセントのP−アニソ
ニトリルを添加したネマチツク液晶組成物。
The liquid crystal temperature range of this liquid crystal composition is 5 to 60°C. Example 3 A nematic liquid crystal composition obtained by adding 5 weight percent of P-anisonitrile to the liquid crystal composition of Example 1.

実施例よりわかるように本発明のネマチツク液晶組成物
は温度範囲が非常に広く、通常の表示体にとつては充分
の温度範囲である。また従来のエステル液晶は過冷却状
態を長時間保持できなかつたので寒冷地での使用は困難
であつた。しかし本発明のネマチツク液晶組成は−20
℃で半日放置しても結晶化しなかつた。このことから本
発明の液晶組成物は寒冷地でも充分使用出来ることがわ
かる。尚本発明の目的は安定で、温度範囲の広い液晶を
作ることにあるが他の目的は1.5V(電池1個)で駆
動出来る液晶を作ることにあつた。
As can be seen from the examples, the nematic liquid crystal composition of the present invention has a very wide temperature range, which is sufficient for ordinary displays. Furthermore, conventional ester liquid crystals could not maintain a supercooled state for a long period of time, making it difficult to use them in cold regions. However, the nematic liquid crystal composition of the present invention is -20
No crystallization occurred even after being left at ℃ for half a day. This shows that the liquid crystal composition of the present invention can be satisfactorily used even in cold regions. The purpose of the present invention is to create a liquid crystal that is stable and has a wide temperature range, but another purpose is to create a liquid crystal that can be driven at 1.5V (one battery).

実施例1の液晶を、ガラス基板の法線に対して85施の
方向からSiOを蒸着したガラス基板により作成したセ
ルに充填し、表示体を作りコントラスト特性を測定した
。この結果を第1図に示す。この図に2おいて、横軸に
は駆動電圧(V)がとつてあり、縦軸には光の透過率(
%)がとつてある。図よりこの液晶を用いた表示体は1
.5で充分駆動出来ることがわかる。以上述べたように
本発明のネマチツク液晶組成物は種々の点で従来の液晶
組成物よりすぐれている。
The liquid crystal of Example 1 was filled in a cell made of a glass substrate on which SiO was vapor-deposited from 85 directions with respect to the normal line of the glass substrate, a display was made, and the contrast characteristics were measured. The results are shown in FIG. In this figure 2, the driving voltage (V) is plotted on the horizontal axis, and the light transmittance (V) is plotted on the vertical axis.
%) is set aside. From the figure, the display using this liquid crystal is 1
.. It can be seen that 5 is sufficient for driving. As described above, the nematic liquid crystal composition of the present invention is superior to conventional liquid crystal compositions in various respects.

このすぐれている本発明のネマチック液晶組成物は腕時
計、電卓等の表示部はもとより種々の民生機器の表示材
料として応用できるものである。尚本発明のネマチツク
液晶組成物を用いた表示体は1.5Vで駆動出来るので
、従来の表示体に必要であつた昇圧回路が必要でなくな
る利点がある。このことからコンパクトにまとめなけれ
ばならない腕時計にとつては本発明のネマチツク液晶組
成物は好適である。本発明のネマチツク液晶組成物を用
いて腕時計を試作して数ケ月の加速試験を行なつたが、
寿命コントラスト等に問題となるところがなかつた。
The excellent nematic liquid crystal composition of the present invention can be applied not only to display parts of wristwatches, calculators, etc., but also as display materials for various consumer appliances. Furthermore, since the display using the nematic liquid crystal composition of the present invention can be driven at 1.5V, there is an advantage that the booster circuit required in the conventional display is not required. For this reason, the nematic liquid crystal composition of the present invention is suitable for wristwatches that must be made compact. A prototype wristwatch was made using the nematic liquid crystal composition of the present invention and accelerated testing was conducted for several months.
There were no problems with life contrast, etc.

この腕時計とそのプロツク図を示すと第2図、第3図の
ようになる。
This wristwatch and its program diagrams are shown in Figures 2 and 3.

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

第1図は電圧とコントラストとの関係を示す。 FIG. 1 shows the relationship between voltage and contrast.

Claims (1)

【特許請求の範囲】 1 少なくとも下記の四種類の液晶を含むことを特徴と
するネマチツク液晶組成物。 1、▲数式、化学式、表等があります▼ (4−n−アルキル安息香酸−4′−シアノフェニルエ
ステル)2、▲数式、化学式、表等があります▼ (4−n−アルキル安息香酸−4′−n−アルコキシフ
ェニルエステル)3、▲数式、化学式、表等があります
▼ (4−n−アルコキシ安息香酸−4′−n−アルキルフ
ェニルエステル)4、▲数式、化学式、表等があります
▼ 4−(4−n−アルキルベンゾイルオキシ)−安息香酸
−2′−クロル−4′−シアノフニルエステル)(但し
、上記式においてR・R′は炭素数3〜9の直鎖アルキ
ル基を示す。 )。
[Scope of Claims] 1. A nematic liquid crystal composition comprising at least the following four types of liquid crystals. 1, ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ (4-n-alkylbenzoic acid-4'-cyanophenyl ester) 2, ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ (4-n-alkylbenzoic acid-4 '-n-alkoxyphenyl ester) 3, ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ (4-n-alkoxybenzoic acid -4'-n-alkylphenyl ester) 4, ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ 4-(4-n-alkylbenzoyloxy)-benzoic acid-2'-chloro-4'-cyanofnyl ester) (However, in the above formula, R and R' represent a straight-chain alkyl group having 3 to 9 carbon atoms. ).
JP2485476A 1976-03-08 1976-03-08 Nematic liquid crystal composition Expired JPS5945020B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2485476A JPS5945020B2 (en) 1976-03-08 1976-03-08 Nematic liquid crystal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2485476A JPS5945020B2 (en) 1976-03-08 1976-03-08 Nematic liquid crystal composition

Publications (2)

Publication Number Publication Date
JPS52107286A JPS52107286A (en) 1977-09-08
JPS5945020B2 true JPS5945020B2 (en) 1984-11-02

Family

ID=12149789

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2485476A Expired JPS5945020B2 (en) 1976-03-08 1976-03-08 Nematic liquid crystal composition

Country Status (1)

Country Link
JP (1) JPS5945020B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58157884A (en) * 1982-03-15 1983-09-20 Chisso Corp Liquid crystal composition

Also Published As

Publication number Publication date
JPS52107286A (en) 1977-09-08

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