JPS604857B2 - Nematic liquid crystal composition - Google Patents
Nematic liquid crystal compositionInfo
- Publication number
- JPS604857B2 JPS604857B2 JP71175A JP71175A JPS604857B2 JP S604857 B2 JPS604857 B2 JP S604857B2 JP 71175 A JP71175 A JP 71175A JP 71175 A JP71175 A JP 71175A JP S604857 B2 JPS604857 B2 JP S604857B2
- 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
Links
Landscapes
- Liquid Crystal (AREA)
- Liquid Crystal Substances (AREA)
Description
【発明の詳細な説明】 本発明は、新規なネマチツ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
広いネマチッ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でき、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。この有望視されてい
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固体から直接
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。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、ネマチック液晶、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。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
。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 inexpensive display materials that can be driven at low voltages. Liquid crystals are currently seen as a promising display material that satisfies this requirement, and liquid crystals are already being used in some displays. This promising liquid crystal is made of organic compounds, but ordinary compounds are solid →
Liquid crystals undergo a phase change from liquid to gas, but liquid crystals do not directly change from solid to liquid, but instead exhibit a phase that has both solid and liquid properties. Due to the difference in molecular orientation of this phase, liquid crystals
It can be divided into smectic liquid crystal, nematic liquid crystal, and cholesteric liquid crystal. 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. 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
。1 従来の白色液晶は主に分子中央にシツフ塩基を有
する化合物であった。Although liquid crystals are very promising as display materials, conventional liquid crystal materials still have the following drawbacks and points for improvement. 1 Conventional white liquid crystals were mainly compounds having a Schiff base at the center of the molecule.
(以下、シツフ液晶と略記する。)しかし、この液晶は
水分の影響を非常に受けやすいので、取扱いやシールド
が非常に難しいという欠点があった。2 比較的安定な
液晶としてアゾキシ化合物系の液晶がある。(Hereinafter, it will be abbreviated as Schiff liquid crystal.) However, this liquid crystal has the drawback that it is extremely susceptible to the influence of moisture, and is therefore extremely difficult to handle and shield. 2. Azoxy compound-based liquid crystals are relatively stable liquid crystals.
(以下、アゾキシ液晶と略記する。)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
っても劣化する欠点がある。この欠点を除去するために
有色のフィルターで表示部を保護しているが、この方法
による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る。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
のこの液晶は温度範囲が限定されており、使用面で制約
を受けていた。(Hereinafter, it will be abbreviated as azoxy liquid crystal.) 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, the display section is protected with a colored filter, but this method has the disadvantage that the entire display section is colored in a specific color, which makes it dark and reduces the display ability. 3. As a liquid crystal that does not have the drawbacks 1 and 2 above, there is a white and very stable ester compound liquid crystal (hereinafter abbreviated as ester liquid crystal), but this conventional liquid crystal has a limited temperature range and cannot be used. were constrained in terms of
例えば、一般式が(Rは直鏡アルキ
ル基である)で表わされる液晶よりなる液晶組成物が考
えられた。For example, a liquid crystal composition comprising a liquid crystal represented by the general formula (R is a straight mirror alkyl group) has been considered.
しかし、この液晶組成物は上限の点(クリヤーポイント
、以下CPと略記する)が50℃以下とCPが低すぎる
欠点を有していた。また、前記液晶化合物に一般式が
(R、R′は直
鎖アルキル基である)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、満足できるものではなかつた。However, this liquid crystal composition had the drawback that the upper limit point (clear point, hereinafter abbreviated as CP) was 50° C. or lower, which was too low. Also, a liquid crystal composition was considered in which a liquid crystal represented by the general formula (R and R' are linear alkyl groups) was mixed with the liquid crystal compound, but this liquid crystal composition also had a CP of 50q.
o or less, which was not satisfactory.
また、アゾキシ液晶やシッフ液晶が過冷却状態を長時間
保持できたのに対して従釆のェステル液晶は長時間の保
持ができなかった。Further, while azoxy liquid crystals and Schiff liquid crystals were able to maintain a supercooled state for a long time, the ester liquid crystal, which is a subordinate liquid crystal, was unable to maintain a supercooled state for a long period of time.
このためェステル液晶を使用した製品は寒冷地での使用
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, it has been difficult to use products using Estel liquid crystal 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1において、記号C、N、1は、それぞれ結晶状態、
ネマチック液晶状態、等万性液体状態を表わす。Table 1 In Table 1, the symbols C, N, and 1 represent crystalline states, respectively.
Represents a nematic liquid crystal state, an isomallic liquid state.
以下の表においても同様である。表1に示した化合物を
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 an example of the components, their proportions, and their properties of a nematic liquid crystal composition of the present invention prepared using the compounds shown in Table 1.
実施例1
この表より、本発明の液晶組成物の融点は−700と、
従来のェステル液晶(融点000)より非常に低いこと
がわかる。Example 1 From this table, the melting point of the liquid crystal composition of the present invention is -700,
It can be seen that the melting point is much lower than the conventional Estel liquid crystal (melting point 000).
また、CPは54qCと5ぴ○を充分確保していること
がわかる。また、過冷却試験を行なったところ、一15
午0で半日(1幼時間)放置しても結晶化しなかった。
このように、本発明の液晶組成物は、従来のェステル液
晶より温度特性の点ですぐれており、シッフ液晶の不安
定性とかアゾキシ液晶の表示能力不足というような欠点
もないので、本発明の液晶組成物は応用範囲の広い表示
材料として使用できるものである。Furthermore, it can be seen that CP sufficiently secures 54qC and 5pi○. In addition, when we conducted a supercooling test, we found that -115
Even if it was left for half a day (one hour) at midnight, it did not crystallize.
As described above, the liquid crystal composition of the present invention is superior to the conventional Estel liquid crystal in terms of temperature characteristics, and has no drawbacks such as the instability of Schiff liquid crystal or the insufficient display ability of azoxy liquid crystal. The composition can be used as a display material with a wide range of applications.
尚、液晶を使用した表示体は、低電圧駆動、低消費電力
等の性質を有するもので、腕時計の表示体として好適で
ある。Note that a display using liquid crystal has properties such as low voltage drive and low power consumption, and is suitable as a display for a wristwatch.
本発明のネマチック液晶組成物を用いて腕時計を作成し
たところ、寿命、コントラストについて数ケ月の加速劣
化試験においても問題となるところがなかった。When a wristwatch was made using the nematic liquid crystal composition of the present invention, there were no problems with respect to lifespan or contrast even after several months of accelerated deterioration tests.
腕時計については、寿命、コントラストの他に応答速度
が問題となるので、応答速度の温度に対する変化を調べ
たところ、第1図のような結果が得られた。従来、ェス
テル液晶は粘度が高いので応答速度がおそいという考え
方が一般的であった。As for wristwatches, in addition to longevity and contrast, response speed is an issue, so we investigated changes in response speed with respect to temperature, and the results shown in Figure 1 were obtained. Conventionally, the general idea was that ester liquid crystals have a high viscosity and therefore have a slow response time.
また、従来のェステル液晶についてなされた実験結果も
その考え方を支持していた。しかし、驚くべきことに本
発明の液晶組成物の応答速度は、従来のェステル液晶は
もとより、シッフ液晶よりも優れており、従来のアゾキ
シ液晶に匹適する速さを示した。比較のために、シッフ
液晶、ァゾキシ液晶の応答速度と温度との関係を示すグ
ラフを第2図、第3図に示す。このことから、本発明の
液晶組成物は腕時計用として特に好適なものであること
がわかる。Furthermore, experimental results conducted on conventional Estel liquid crystals also supported this idea. However, surprisingly, the response speed of the liquid crystal composition of the present invention was superior not only to the conventional Estel liquid crystal but also to the Schiff liquid crystal, and showed a speed comparable to the conventional azoxy liquid crystal. For comparison, graphs showing the relationship between the response speed and temperature of Schiff liquid crystal and Azoxy liquid crystal are shown in FIGS. 2 and 3. This shows that the liquid crystal composition of the present invention is particularly suitable for use in wristwatches.
第1図は、本発明の液晶組成物の応答速度と温 .度と
の関係を示す図。
第2図は、従釆のシッフ液晶の応答速度と温度との関係
を示す図。第3図は、従来のアゾキシ液晶の応答速度と
温度との関係を示す図。第1図〜第3図において、縦軸
は対数目盛にとってある。髪1図
髪2図
冬3図FIG. 1 shows the response speed and temperature of the liquid crystal composition of the present invention. A diagram showing the relationship with degree. FIG. 2 is a diagram showing the relationship between the response speed and temperature of a secondary Schiff liquid crystal. FIG. 3 is a diagram showing the relationship between response speed and temperature of a conventional azoxy liquid crystal. In FIGS. 1 to 3, the vertical axis is on a logarithmic scale. Hair 1 Figure Hair 2 Figure Winter 3
Claims (1)
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 being composed of a compound represented by the following.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP71175A JPS604857B2 (en) | 1974-12-26 | 1974-12-26 | 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 |
|---|---|---|---|
| JP71175A JPS604857B2 (en) | 1974-12-26 | 1974-12-26 | Nematic liquid crystal composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5175682A JPS5175682A (en) | 1976-06-30 |
| JPS604857B2 true JPS604857B2 (en) | 1985-02-07 |
Family
ID=11481338
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP71175A Expired JPS604857B2 (en) | 1974-12-23 | 1974-12-26 | Nematic liquid crystal composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS604857B2 (en) |
-
1974
- 1974-12-26 JP JP71175A patent/JPS604857B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5175682A (en) | 1976-06-30 |
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