JPH0443325A - Ferroelectric liquid crystal element - Google Patents

Ferroelectric liquid crystal element

Info

Publication number
JPH0443325A
JPH0443325A JP15194790A JP15194790A JPH0443325A JP H0443325 A JPH0443325 A JP H0443325A JP 15194790 A JP15194790 A JP 15194790A JP 15194790 A JP15194790 A JP 15194790A JP H0443325 A JPH0443325 A JP H0443325A
Authority
JP
Japan
Prior art keywords
liquid crystal
ferroelectric liquid
alignment
ferroelectric
manufactured
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
JP15194790A
Other languages
Japanese (ja)
Inventor
Masao Yamamoto
雅夫 山本
Hideaki Mochizuki
望月 秀晃
Yuji Satani
裕司 佐谷
Katsuji Hattori
服部 勝治
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP15194790A priority Critical patent/JPH0443325A/en
Publication of JPH0443325A publication Critical patent/JPH0443325A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the ferroelectric color liquid crystal element which has a superior color tone by holding a ferroelectric liquid crystal material in the gap between a couple of opposite liquid crystal support plates which have films of specific polyamide. CONSTITUTION:At least one liquid crystal support plate 15 is coated with polyamide to a 0.5 - 30nm film thickness, an orientation process is carried out to form an orientation control film 13, and an amine compound is added preferably to pyrimidine-based liquid crystal. Therefore, molecules of polyamide or its aggregate are oriented excellently and when the liquid crystal element is formed by using this orientation control film 13, uniform orientation is easily obtained over the entire surface of the liquid crystal element. Consequently, the large- sized color liquid display device which has the superior color tone is obtained.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は強誘電性液晶素子に関するものである。[Detailed description of the invention] Industrial applications The present invention relates to a ferroelectric liquid crystal element.

従来の技術 従来分子やその集合体などの配向を制御する技術として
、液晶素子においては、ポリアミック酸などのポリアミ
ドを基板に塗布し、250℃前後の高温でイミド化した
ポリイミドの表面を布などでこすって配向制御を行なう
ラビング処理を行なった配向制御膜が主に用いられてい
る。
Conventional technology Conventionally, as a technology for controlling the orientation of molecules and their aggregates, etc., in liquid crystal elements, polyamide such as polyamic acid is applied to the substrate, and the surface of the polyimide is imidized at a high temperature of around 250°C with a cloth or the like. An alignment control film that has been subjected to a rubbing treatment in which alignment is controlled by rubbing is mainly used.

発明が解決しようとする課題 液晶素子において、液晶分子などの配向を制御する方法
の一つであるラビング処理は単純な方法であるため、低
コストで実施でき、従来からTN型などの液晶素子にお
いて膜厚が約30〜1100nのポリイミドが配向制御
膜として用いられている。しかし、分子の配向方向に双
安定性を必要とする、強誘電性を示す液晶を用いた液晶
素子においては、上記の配向制御膜では、この双安定性
の発現が不十分であるという課題があった。また、ポリ
イミドは一般に溶剤に不溶性のため、ポリイミドを液晶
素子の配向制御m膜に用いるにはポリイミドの前駆体で
あるポリアミック酸などのポリアミドの溶液をスピンナ
塗布などの方法によりガラス基板上に塗布し、250°
C前後の高温で焼成しなければならず、カラー液晶素子
の製作に用いるカラーフィルタは、一般に耐熱温度が低
くて、従来のポリイミド成膜法では、カラーフィルタの
選択範囲が狭くなり色調の優れたカラー液晶素子の実現
は困難であるという課題があった。
Problems to be Solved by the Invention Rubbing treatment, which is one of the methods for controlling the orientation of liquid crystal molecules in liquid crystal elements, is a simple method that can be carried out at low cost. Polyimide having a thickness of about 30 to 1100 nm is used as the alignment control film. However, in liquid crystal devices using ferroelectric liquid crystals that require bistability in the orientation direction of molecules, the above-mentioned alignment control film has the problem of insufficient expression of this bistability. there were. Furthermore, since polyimide is generally insoluble in solvents, in order to use polyimide as an alignment control film for liquid crystal devices, a solution of polyamide such as polyamic acid, which is a precursor of polyimide, must be applied onto a glass substrate using a method such as spinner coating. , 250°
Color filters used in the production of color liquid crystal devices generally have a low heat resistance, and the conventional polyimide film formation method narrows the selection range of color filters, making it difficult to produce color filters with excellent color tone. The problem was that it was difficult to realize a color liquid crystal element.

本発明はこのような課題を解決するもので3強誘電性液
晶の双安定性を発現する配向制御膜を低温で形成するこ
とにより、色調の優れた強誘電性カラー液晶素子を提供
することを目的とするものである。
The present invention solves these problems and aims to provide a ferroelectric color liquid crystal element with excellent color tone by forming an alignment control film that exhibits the bistability of 3 ferroelectric liquid crystals at a low temperature. This is the purpose.

課題を解決するための手段 この課題を解決するために本発明の強誘電性液晶素子は
少なくとも一方の液晶支持板上に膜厚が0.5〜20n
mになるようポリアミドを塗布し、配向処理をして配向
制御膜とし、さらにピリミジン系の液晶で、アミン化合
物を添加したものである。
Means for Solving the Problem In order to solve this problem, the ferroelectric liquid crystal element of the present invention has a film thickness of 0.5 to 20 nm on at least one liquid crystal support plate.
Polyamide was coated so as to have an orientation of m, and an alignment control film was obtained by applying an alignment treatment.Furthermore, it was made of pyrimidine-based liquid crystal and an amine compound was added thereto.

作用 本発明はポリアミドの塗膜を用い、その塗膜に配向処理
を施した配向制御IMで、とくにその膜厚を0.5〜2
0nmにすることが重要な特徴である。
Function The present invention is an orientation control IM in which a polyamide coating film is used and the coating film is subjected to an orientation treatment.
An important feature is that the thickness is 0 nm.

このように薄膜化することにより、ポリアミドの分子や
その集合体の良好な配向を実現することができる。また
、この配向制msを用いて液晶素子を作成した場合、液
晶素子の全面にわたって均一な配向を容易に低コストで
実現できる。中でも、強誘電性を示す液晶を用いた液晶
素子では、双安定性を完全に保持したままで均一な配向
を低コストで実現できる。さらに、塗膜の熱焼成を行な
わなくてもよいので、液晶素子のカラー化に際して、カ
ラーフィルタの選択範囲を拡大できることとなる。
By making the film thinner in this manner, it is possible to achieve good orientation of polyamide molecules and their aggregates. Further, when a liquid crystal element is produced using this alignment control ms, uniform alignment can be easily achieved over the entire surface of the liquid crystal element at low cost. Among these, liquid crystal elements using liquid crystals exhibiting ferroelectric properties can achieve uniform alignment at low cost while completely maintaining bistability. Furthermore, since there is no need to thermally bake the coating film, the selection range of color filters can be expanded when colorizing the liquid crystal element.

実施例 以下本発明の一実施例の配向制御膜およびそれを用いた
液晶素子について、図面を参照しながら説明する。第1
図は本発明の一実施例である配向制御膜を用いた液晶素
子の構成を示す0図に示すようにガラスやプラスチック
などで作成した基板11上にインジウム、錫酸化物(以
後ITOと略す)よりなる透明電極12を形成し、その
上に配向制?[1M13を形成後配向処理を施し、スペ
ーサ兼シール樹脂14を印刷し、2枚の液晶支持板15
を貼合わせ、開口部より液晶16を注入後、開口部を封
止していわゆる強誘電性液晶セルを作製した。このよう
にして完成した強誘電性液晶素子は注入する強誘電性液
晶にシクロヘキシルアミン、ベンジルアミン フェニル
プロピルアミンベンジルエタノールアミン ポリオキシ
プロピレンポリアミンのアミンのうち一種もしくは数種
の混合物を添加剤として加えることで長期間双安定性を
保持することができる。
EXAMPLE Hereinafter, an alignment control film according to an example of the present invention and a liquid crystal device using the same will be described with reference to the drawings. 1st
The figure shows the structure of a liquid crystal element using an alignment control film, which is an embodiment of the present invention.As shown in figure 0, indium and tin oxide (hereinafter abbreviated as ITO) are deposited on a substrate 11 made of glass, plastic, etc. A transparent electrode 12 consisting of a transparent electrode 12 is formed thereon, and an orientation control layer 12 is formed thereon. [After forming 1M13, an alignment treatment is performed, a spacer/sealing resin 14 is printed, and two liquid crystal support plates 15 are formed.
were bonded together, liquid crystal 16 was injected through the opening, and the opening was sealed to produce a so-called ferroelectric liquid crystal cell. The ferroelectric liquid crystal device thus completed can be produced by adding one or a mixture of amines such as cyclohexylamine, benzylamine, phenylpropylamine, benzylethanolamine, and polyoxypropylene polyamine to the ferroelectric liquid crystal to be injected. It can maintain bistability for a long period of time.

(実施例1) 市販の全芳香族系ポリアミック酸(日産化学社製RN7
15)を専用のシンナで希釈し、0.3重量%のポリア
ミック酸の溶液を調整した。ついで、この溶液を[TO
電極のパターンを形成したガラス基板にスピンナで25
00回転/分で1分間回転塗布を行なった。塗布後80
℃で15分間乾燥を行ない溶媒を蒸発させポリアミック
酸の2!膜をガラス基板表面上に形成した0M厚は6n
mであった。その後、このボリアミンク酸の塗膜が形成
された表面をレーヨンの布を用いて同一方向に10回摩
擦してラビング処理を行い配向制御膜を完成した。この
ようにしてポリアミック酸の配向制御1膜を形成したガ
ラス液晶支持板を2枚用意し第2図に示すようにその片
方の支持板(例えば下側液晶支持板22)の配向制御膜
を形成した面にスペーサ兼シール樹脂25として直径2
μmのガラスramを分散した酸無水物硬化型エポキシ
樹脂を1辺のみ辺の中央に5−の幅を残して印刷し他の
周辺には0.2閣幅で印刷した上で、上側液晶支持板2
1と下側支持板22に形成した配向制御膜のラビング処
理方向23.24が平行でかつ配向制御膜面を対向させ
た状態で加圧し、140℃で4時間加熱して硬化接着し
た。接着後、液晶が等方性を示す温度すなわち80℃付
近まで支持板を加熱し、開口部から液晶(メルク社製、
商品名ZLI3654)を注入した。注入後、室温まで
徐冷し開口部を市販の酸無水物硬化型エポキシ樹脂で封
止し、強誘電性液晶セルを完成した。二のようにして完
成した強誘電性液晶セルは、配向ムラのない良好な配向
状態を示し、電圧印加により、双安定性の保持した良好
な電気光学特性が得られた。
(Example 1) Commercially available wholly aromatic polyamic acid (RN7 manufactured by Nissan Chemical Co., Ltd.)
15) was diluted with a special thinner to prepare a 0.3% by weight polyamic acid solution. This solution was then diluted with [TO
A spinner was used to attach the glass substrate with the electrode pattern for 25 minutes.
Spin coating was carried out for 1 minute at 00 revolutions/minute. 80 after application
Dry at ℃ for 15 minutes to evaporate the solvent and prepare 2! of polyamic acid. The thickness of the film formed on the surface of the glass substrate is 6n.
It was m. Thereafter, the surface on which the polyaminic acid coating was formed was rubbed 10 times in the same direction using a rayon cloth to perform a rubbing treatment to complete an orientation control film. Two glass liquid crystal support plates each having one polyamic acid alignment control film formed thereon are prepared in this way, and an alignment control film is formed on one of the support plates (for example, the lower liquid crystal support plate 22) as shown in FIG. A spacer/sealing resin 25 with a diameter of 2
Acid anhydride-curing epoxy resin with μm glass RAM dispersed in it was printed leaving a 5-mm width in the center of one side, and 0.2mm width on the other periphery, and then the upper liquid crystal support was printed. Board 2
The rubbing directions 23 and 24 of the alignment control films formed on 1 and the lower support plate 22 were parallel to each other, and the surfaces of the alignment control films were pressed against each other and heated at 140° C. for 4 hours to cure and bond. After adhesion, the support plate is heated to the temperature at which the liquid crystal exhibits isotropy, that is, around 80°C, and the liquid crystal (manufactured by Merck & Co., Ltd.,
(trade name: ZLI3654) was injected. After injection, it was slowly cooled to room temperature and the opening was sealed with a commercially available acid anhydride-curable epoxy resin to complete a ferroelectric liquid crystal cell. The ferroelectric liquid crystal cell completed in step 2 showed a good alignment state with no alignment unevenness, and when voltage was applied, good electro-optical properties with bistability maintained were obtained.

(実施例2) 市販の全芳香族系ポリアミック酸(日量化学社製RN7
15)を用いて実施例1と同様の操作により配向処理さ
れたポリアミック酸の配向制御膜を形成したガラス液晶
支持板を2枚用意し、第2図に示すようにその片方の支
持板(例えば下側液晶支持板22)の配向制御膜を形成
した面にスペーサ兼シール樹脂25として直径2t!m
のガラス繊維を分散した紫外線硬化型エポキシ樹脂を1
辺のみ辺の中央に5■の幅を残して印刷し、他の周辺に
0.2腫幅で印刷した上で、上側液晶支持板21と下側
支持板22に形成した配向制御膜のラビング処理方向2
3.24が平行でかつ配向制御膜面を対向させた状態で
加圧し、紫外線を照射し硬化接着した。接着後、液晶が
等方性を示す温度すなわち80℃付近まで支持板を加熱
し、開口部から液晶(メルク社製、商品名ZLI365
4)を注入した。注入後、室温まで徐冷し開口部を市販
の紫外線硬化型エポキシ樹脂で封止し、強誘電性液晶セ
ルを完成した。このようにして完成した強誘電性液晶セ
ルは、配向ムラのない良好な配向状態を示し、電圧印加
により、双安定性が保持された良好な電気光学特性が得
られた。
(Example 2) Commercially available wholly aromatic polyamic acid (RN7 manufactured by Nichikagaku Co., Ltd.)
Prepare two glass liquid crystal support plates on which are formed orientation control films of polyamic acid that have been subjected to alignment treatment using the same procedure as in Example 1 using 15), and as shown in FIG. A spacer/sealing resin 25 with a diameter of 2t is placed on the surface of the lower liquid crystal support plate 22) on which the alignment control film is formed. m
1 UV-curable epoxy resin with glass fibers dispersed in it.
After printing with a width of 5 cm left in the center of the sides and printing with a width of 0.2 cm around the other edges, rubbing the alignment control film formed on the upper liquid crystal support plate 21 and the lower support plate 22. Processing direction 2
3.24 were parallel and the orientation control film surfaces were placed opposite each other, pressure was applied, and ultraviolet rays were irradiated to cure and bond. After adhesion, the support plate is heated to the temperature at which the liquid crystal exhibits isotropy, that is, around 80°C, and the liquid crystal (manufactured by Merck & Co., trade name: ZLI365) is inserted through the opening.
4) was injected. After injection, the solution was slowly cooled to room temperature and the opening was sealed with a commercially available UV-curable epoxy resin to complete a ferroelectric liquid crystal cell. The ferroelectric liquid crystal cell thus completed showed a good alignment state with no alignment unevenness, and when voltage was applied, good electro-optical properties with bistability maintained were obtained.

(実施例3) 市販のポリアミック酸(日量化学社製 RN715)を専用のシンナで希釈し、1.0重量%の
ポリアミック酸の溶液を調整した。ついで、この溶液を
ITO電極のパターンを形成したガラス基板にスピンナ
で2500回転/分で1分間回転塗布を行なった。塗布
後80℃で15分間乾燥を行ない溶媒を蒸発させポリア
ミック酸の塗膜をガラス基板表面上に形成した。膜厚は
20nmであった。以下具体的実施例1および具体的実
施例2と同様の操作により作製した強誘電性液晶セルは
、配向ムラのない良好な配向状態を示し、電圧印加によ
り、双安定性が保持された良好な電気光学特性が得られ
た。
(Example 3) A commercially available polyamic acid (RN715, manufactured by Nichikagaku Co., Ltd.) was diluted with a special thinner to prepare a 1.0% by weight polyamic acid solution. Next, this solution was spin-coated for 1 minute at 2500 revolutions/minute using a spinner onto a glass substrate on which an ITO electrode pattern was formed. After coating, it was dried at 80° C. for 15 minutes to evaporate the solvent and form a coating film of polyamic acid on the surface of the glass substrate. The film thickness was 20 nm. The ferroelectric liquid crystal cells produced by the same operations as those in Specific Example 1 and Specific Example 2 below exhibited a good alignment state with no alignment unevenness, and when voltage was applied, a good alignment state with maintained bistability was obtained. Electro-optical properties were obtained.

(実施例4) 市販のポリアミック酸(日量化学社製 RN715)を用いて、実施例1および具体的実施例2
と同様の操作により0作製た強誘電性液晶セルに添加剤
としてシクロヘキンルアミンを0.1重置%添加した液
晶(メルク社製、商品名ZLI3654)を注入した。
(Example 4) Using commercially available polyamic acid (RN715 manufactured by Nichikagaku Co., Ltd.), Example 1 and Specific Example 2 were prepared.
A liquid crystal (manufactured by Merck & Co., trade name: ZLI3654) to which 0.1 weight percent of cyclohexylamine was added as an additive was injected into a ferroelectric liquid crystal cell prepared in the same manner as above.

このようにして完成した強誘電性液晶セルは、配向ムラ
のない良好な配向状態を示し、電圧印加により、双安定
性が保持された良好な電気光学特性が得られ、さらに長
期間にわたり双安定性が保持された。
The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness, and when a voltage is applied, good electro-optical properties that maintain bistability are obtained, and it is also bistable for a long period of time. gender was preserved.

(実施例5) 市販のボリアミンク酸(日量化学社製 RN715)を用いて、実施例1および実施例2と同様
の操作により作製した強誘電性液晶セルに添加剤として
ベンジルアミンを0.3重量%添加した液晶(メルク社
製、商品名ZLI3654)を注入した。このようにし
て完成した強誘電性液晶セルは、配向ムラのない良好な
配向状態を示し、電圧印加により、双安定性が保持され
た良好な電気光学特性が得られ、さらに長期間にわたり
双安定性が保持された。
(Example 5) 0.30% benzylamine was added as an additive to a ferroelectric liquid crystal cell prepared in the same manner as in Examples 1 and 2 using commercially available polyamic acid (RN715 manufactured by Nichikagaku Co., Ltd.). A liquid crystal (manufactured by Merck & Co., trade name: ZLI3654) added in weight percent was injected. The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness, and when a voltage is applied, good electro-optical properties that maintain bistability are obtained, and it is also bistable for a long period of time. gender was preserved.

(実施例6) 市販のポリアミック酸(日量化学社製 RN7 ] 5)を用いて、実施例1および実施例2と
同様の操作により作製した強誘電性液晶セルIこ添加剤
として分子量400のポリオキシプロピレンジアミンを
0.1重量%添加した液晶(メルク社製、商品名ZLI
3654)を注入した。このようにして完成した強誘電
性液晶セルは、配向ムラのない良好な配向状態を示し、
電圧印加により、双安定性が保持された良好な電気光学
特性が得られ、さらに長期間にわたり双安定性が保持さ
れた。
(Example 6) A ferroelectric liquid crystal cell I was prepared using a commercially available polyamic acid (RN7 manufactured by Nichikagaku Co., Ltd.) in the same manner as in Examples 1 and 2. Liquid crystal containing 0.1% by weight of polyoxypropylene diamine (manufactured by Merck & Co., trade name: ZLI)
3654) was injected. The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness,
By applying a voltage, good electro-optical properties with maintained bistability were obtained, and the bistability was maintained for a long period of time.

(実施例7) 市販のポリアミック酸(日量化学社製 RN715)を用いて、実施例1および実施例2と同様
の操作により作製した強誘電性液晶セルに添加剤として
分子量230のポリオキシプロピレンジアミンを0.3
重量%添加した液晶(メルク社製、商品名ZLI365
4)を注入した。このようにして完成した強誘電性液晶
セルは、配向ムラのない良好な配向状態を示し、電圧印
加により、双安定性が保持された良好な電気光学特性が
得られ、さらに長期間にわたり双安定性が保持された。
(Example 7) Polyoxypropylene with a molecular weight of 230 was added as an additive to a ferroelectric liquid crystal cell prepared in the same manner as in Examples 1 and 2 using commercially available polyamic acid (RN715 manufactured by Nichikagaku Co., Ltd.). 0.3 diamine
Liquid crystal with added weight% (manufactured by Merck & Co., trade name ZLI365)
4) was injected. The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness, and when a voltage is applied, good electro-optical properties that maintain bistability are obtained, and it is also bistable for a long period of time. gender was preserved.

(実施例8) 市販のポリアミック酸(日産化学社製 SE4110)を専用のシンナで希釈し、0.3重量%
のポリアミック酸の溶液を調整した。その後、実施例1
と同様の条件で回転塗布を行ないITOパターンの形成
したガラス基板上にポリアミック酸の塗膜を形成した。
(Example 8) Commercially available polyamic acid (SE4110 manufactured by Nissan Chemical Co., Ltd.) was diluted with a special thinner to give a concentration of 0.3% by weight.
A solution of polyamic acid was prepared. After that, Example 1
A coating film of polyamic acid was formed on a glass substrate on which an ITO pattern was formed by spin coating under the same conditions as described above.

膜厚は6nmであった。以下実施例1および実施例2と
同様の操作により、作製した強誘電性液晶セルに液晶(
メルク社製。
The film thickness was 6 nm. Hereinafter, by the same operation as in Example 1 and Example 2, the liquid crystal (
Manufactured by Merck.

商品名ZLI3654)を注入した。このようにして完
成した強誘電性液晶セルは、配向ムラのない良好な配向
状態を示し、電圧印加により、双安定性が保持された良
好な電気光学特性が得られた。
(trade name: ZLI3654) was injected. The ferroelectric liquid crystal cell thus completed showed a good alignment state with no alignment unevenness, and when voltage was applied, good electro-optical properties with bistability maintained were obtained.

(実施例9) 市販のポリアミック酸(日産化学社製 SE4110)を専用のシンナで希釈し、1.0重量%
のポリアミック酸の溶液を調整した。その後、実施例1
と同様の条件で回転塗布を行ないITOパターンの形成
したガラス基板上にポリアミック酸の塗膜を形成した。
(Example 9) Commercially available polyamic acid (SE4110 manufactured by Nissan Chemical Co., Ltd.) was diluted with a special thinner to give a concentration of 1.0% by weight.
A solution of polyamic acid was prepared. After that, Example 1
A coating film of polyamic acid was formed on a glass substrate on which an ITO pattern was formed by spin coating under the same conditions as described above.

膜厚は20nmであった。The film thickness was 20 nm.

以下具体的実施例1および具体的実施例2と同様の操作
により、作製した強誘電性液晶セルに液晶(メルク社製
、商品名ZLr3654)を注入した。このようにして
完成した強誘電性液晶セルは、配向ムラのない良好な配
向状態を示し、電圧印加により、双安定性が保持された
良好な電気光学特性が得られた。
Thereafter, a liquid crystal (manufactured by Merck & Co., trade name: ZLr3654) was injected into the produced ferroelectric liquid crystal cell by the same operations as in Specific Example 1 and Specific Example 2. The ferroelectric liquid crystal cell thus completed showed a good alignment state with no alignment unevenness, and when voltage was applied, good electro-optical properties with bistability maintained were obtained.

(実施例10) 市販のポリアミック酸(日産化学社製 SE4110)を用いて、実施例1および実施例2と同
様の操作により作製した強誘電性液晶セルに添加剤とし
てシクロヘキシルアミンを0.1重量%添加した液晶(
メルク社製、商品名 ZLI3654)を注入した。このようにして完成した
強誘電性液晶セルは、配向ムラのない良好な配向状態を
示し、電圧印加により、双安定性が保持された良好な電
気光学特性が得られ、さらに長期間にわたり双安定性が
保持された。
(Example 10) 0.1 weight of cyclohexylamine was added as an additive to a ferroelectric liquid crystal cell prepared in the same manner as in Examples 1 and 2 using commercially available polyamic acid (SE4110 manufactured by Nissan Chemical Co., Ltd.). % added liquid crystal (
Merck & Co., trade name ZLI3654) was injected. The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness, and when a voltage is applied, good electro-optical properties that maintain bistability are obtained, and it is also bistable for a long period of time. gender was preserved.

(実施例11) 市販のポリアミック酸(日産化学社製 SE4110)を用いて、実施例1および実施例2と同
様の操作により作製した強誘電性液晶セルに添加剤とし
てヘンシルアミンを0.3重量%添加した液晶(メルク
社製、商品名ZLI3654)を注入した。このように
して完成した強誘電性液晶セルは、配向ムラのない良好
な配向状態を示し、電圧印加により、双安定性が保持さ
れた良好な電気光学特性が得られ、さらに長期間にわた
り双安定性が保持された。
(Example 11) 0.3% by weight of hensylamine was added as an additive to a ferroelectric liquid crystal cell prepared using commercially available polyamic acid (SE4110 manufactured by Nissan Chemical Co., Ltd.) in the same manner as in Examples 1 and 2. The added liquid crystal (manufactured by Merck & Co., trade name: ZLI3654) was injected. The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness, and when a voltage is applied, good electro-optical properties that maintain bistability are obtained, and it is also bistable for a long period of time. gender was preserved.

(実施例12) 市販のポリアミック酸(日産化学社製 SE4110)を用いて、実施例1および実施例2と同
様の操作により作製した強誘電性液晶セルに添加剤とし
て分子量400のポリオキシプロピレンジアミンを0.
1重量%添加した液晶(メルク社製、商品名zLr36
54)を注入した。このようにして完成した強誘電性液
晶セルは、配向ムラのない良好な配向状態を示し、電圧
印加により、双安定性が保持された良好な電気光学特性
が得られ、さらに長期間にわたり双安定性が保持された
(Example 12) Polyoxypropylene diamine with a molecular weight of 400 was added as an additive to a ferroelectric liquid crystal cell prepared in the same manner as in Examples 1 and 2 using commercially available polyamic acid (SE4110 manufactured by Nissan Chemical Co., Ltd.). 0.
Liquid crystal containing 1% by weight (manufactured by Merck & Co., trade name zLr36)
54) was injected. The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness, and when a voltage is applied, good electro-optical properties that maintain bistability are obtained, and it is also bistable for a long period of time. gender was preserved.

(実施例13) 市販のポリアミック酸(日産化学社製 SE4110)を用いて、実施例1および実施例2と同
様の操作により作製した強誘電性液晶セルに添加剤とし
て分子量230のポリオキシプロピレンジアミンを0,
3重量%添加した液晶(メルク社製、商品名ZLI36
54)を注入した。このようにして完成した強誘電性液
晶セルは、配向ムラのない良好な配向状態を示し、電圧
印加により、双安定性が保持された良好な電気光学特性
が得られ、さらに長期間にわたり双安定性が保持された
(Example 13) Polyoxypropylene diamine with a molecular weight of 230 was added as an additive to a ferroelectric liquid crystal cell prepared using commercially available polyamic acid (SE4110 manufactured by Nissan Chemical Co., Ltd.) in the same manner as in Examples 1 and 2. 0,
Liquid crystal containing 3% by weight (manufactured by Merck & Co., trade name: ZLI36)
54) was injected. The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness, and when a voltage is applied, good electro-optical properties that maintain bistability are obtained, and it is also bistable for a long period of time. gender was preserved.

(実施例14) 0.5gのN−アルコキシメチル変性ナイロンを99.
5gのメチルアルコールに溶かし、0.5重置%のN−
アルコキシメチル変性ナイロンのメタン−ル溶液を調整
した。ついで、この溶液をITO電極のパターンを形成
したガラス基板に2500回転/分で1分間回転塗布を
行なった。v!布後後110°C30分間乾燥を行ない
溶媒を蒸発させN−アルコキシメチル変性ナイロンの塗
膜をガラス基板表面上に形成した。膜厚は10nmであ
った。その後、このN−アルコキシメチル変性ナイロン
のy!膜が形成された表面をレーヨンの布を用いて同一
方向に10回ラビング処理を行ない配向制御膜を完成し
た。こうしてN−アルコキシメチル変性ナイロンの配向
制御膜を形成したガラス液晶支持板を2枚用意し第2図
に示すようにその片方の支持板(例えば下側液晶支持v
i22)の配向制御膜を形成した面にスペーサ兼シール
樹脂25として直径2μmのガラス繊維を分散した酸無
水物硬化型エポキシ樹脂を1辺のみ辺の中央に5II1
1の幅を残して他の周辺に0.2震幅で印刷した上で、
上側液晶支持板21と下側支持板22に形成した配向制
御膜のラビング処理方向23.24が平行でかつ配向制
御膜面を対向させた状態で加圧し、140℃で4時間加
熱して硬化接着した。接着後、支持板を液晶が等方性を
示す温度すなわち80°C付近まで加熱し、開口部から
液晶(メルク社製。
(Example 14) 0.5 g of N-alkoxymethyl modified nylon was heated to 99.9%.
Dissolved in 5 g of methyl alcohol, 0.5% N-
A methanol solution of alkoxymethyl-modified nylon was prepared. Next, this solution was spin-coated for 1 minute at 2500 revolutions/minute onto a glass substrate on which an ITO electrode pattern was formed. v! After washing, the cloth was dried at 110 DEG C. for 30 minutes to evaporate the solvent and form a coating film of N-alkoxymethyl modified nylon on the surface of the glass substrate. The film thickness was 10 nm. After that, the y! The surface on which the film was formed was rubbed 10 times in the same direction using a rayon cloth to complete an orientation control film. Two glass liquid crystal support plates on which alignment control films of N-alkoxymethyl-modified nylon are formed are prepared in this way, and one of the support plates (for example, the lower liquid crystal support v
On the surface on which the orientation control film of i22) is formed, an acid anhydride-curing epoxy resin in which glass fibers with a diameter of 2 μm are dispersed is applied as a spacer/sealing resin 25 in the center of only one side.
After printing with a width of 0.2 on the other peripheries, leaving a width of 1,
The rubbing directions 23 and 24 of the alignment control films formed on the upper liquid crystal support plate 21 and the lower support plate 22 are parallel to each other, and the surfaces of the alignment control films are pressed and heated at 140° C. for 4 hours to cure. Glued. After bonding, the support plate is heated to a temperature at which the liquid crystal exhibits isotropy, that is, around 80°C, and the liquid crystal (manufactured by Merck & Co., Ltd.) is inserted through the opening.

商品名ZLI3654)を注入した。注入後、室温まで
徐冷し開口部を市販の酸無水物硬化型エポキシ樹脂で封
止し、強誘電性液晶セルを完成した。
(trade name: ZLI3654) was injected. After injection, it was slowly cooled to room temperature and the opening was sealed with a commercially available acid anhydride-curable epoxy resin to complete a ferroelectric liquid crystal cell.

このようにして完成した強誘電性液晶セルは、配向ムラ
のない良好な配向状態を示し、電圧印加により、双安定
性が保持された良好な電気光学特性が得られた。
The ferroelectric liquid crystal cell thus completed showed a good alignment state with no alignment unevenness, and when voltage was applied, good electro-optical properties with bistability maintained were obtained.

(実施例15) N−アルコキシメチル変性ナイロンを用いて実施例14
と同様の操作により配向処理されたN−アルコキシメチ
ル変性ナイロンの配向制御膜を形成したガラス液晶支持
板を2枚用意し第2図に示すようにその片方の支持板(
例えば下側液晶支持板22)の配向制御膜を形成した面
にスペーサ兼シール樹脂25として直径2μmのガラス
繊維を分散した紫外線硬化型エポキシ樹脂を1辺のみ辺
の中央に5mの幅を残して他の周辺に0.2m幅で印刷
した上で、上側液晶支持板21と下側支持板22に形成
した配向制御膜のラビング処理方向23.24が平行で
かつ配向側′a膜面を対向させた状態で加圧し、紫外線
を照射し硬化接着した。
(Example 15) Example 14 using N-alkoxymethyl modified nylon
Prepare two glass liquid crystal support plates on which are formed alignment control films of N-alkoxymethyl modified nylon that have been subjected to alignment treatment in the same manner as above, and as shown in Figure 2, one of the support plates (
For example, on the surface of the lower liquid crystal support plate 22) on which the alignment control film is formed, an ultraviolet curing epoxy resin in which glass fibers with a diameter of 2 μm are dispersed is applied as a spacer/sealing resin 25, leaving a width of 5 m in the center of only one side. After printing with a width of 0.2 m on the other periphery, the rubbing directions 23 and 24 of the alignment control films formed on the upper liquid crystal support plate 21 and the lower support plate 22 are parallel and the alignment side 'a film surfaces are opposite to each other. In this state, pressure was applied and ultraviolet rays were irradiated to cure and bond.

接着後、液晶が等方性を示す温度すなわち80 ′C付
近まで支持板を加熱し、開口部から液晶(メルク社製、
商品名ZLI3654)を注入した。注入後、室温まで
徐冷し開口部を市販の紫外線硬化型エポキシ樹脂で封止
し、強誘電性液晶セルを完成した。このようにして完成
した強誘電性液晶セルは、配向ムラのない良好な配向状
態を示し、電圧印加により、双安定性が保持された良好
な電気光学特性が得られた。
After bonding, the support plate is heated to the temperature at which the liquid crystal exhibits isotropy, that is, around 80'C, and the liquid crystal (manufactured by Merck & Co., Ltd.,
(trade name: ZLI3654) was injected. After injection, the solution was slowly cooled to room temperature and the opening was sealed with a commercially available UV-curable epoxy resin to complete a ferroelectric liquid crystal cell. The ferroelectric liquid crystal cell thus completed showed a good alignment state with no alignment unevenness, and when voltage was applied, good electro-optical properties with bistability maintained were obtained.

(実施例16) 1:OgのN−アルコキシメチル変性ナイロンを99.
0gのメチルアルコールに溶かし、1.0重量%のN−
アルコキシメチル変性ナイロンのメタノール溶液を調製
した。次いで、この溶液をITO電極のパターンを形成
したガラス基板に2500回転/分で1分間回転塗布を
行なった。塗布後110°Cで30分間乾燥を行ない溶
媒を蒸発させN−アルコキシメチル変性ナイロンの塗膜
をガラス基板表面上に形成した。膜厚は20nmであっ
た。以下実施例14および実施例15と同様の操作によ
り作製した強誘電性液晶セルは、配向ムラのない良好な
配向状態を示し、電圧印加により、双安定性が保持され
た良好な電気光学特性が得られた。
(Example 16) 1:Og N-alkoxymethyl modified nylon with 99.
Dissolved in 0g of methyl alcohol, 1.0% by weight of N-
A methanol solution of alkoxymethyl-modified nylon was prepared. Next, this solution was spin-coated for 1 minute at 2500 rpm on a glass substrate on which an ITO electrode pattern was formed. After coating, it was dried at 110°C for 30 minutes to evaporate the solvent and form a coating film of N-alkoxymethyl modified nylon on the surface of the glass substrate. The film thickness was 20 nm. The ferroelectric liquid crystal cells produced by the same operations as in Examples 14 and 15 exhibited a good alignment state with no alignment unevenness, and when voltage was applied, good electro-optical properties with bistability maintained were obtained. Obtained.

(実施例17) N−アルコキシメチル変性ナイロンを用いて、実施例1
4および実施例15と同様の操作により作製した強誘電
性液晶セルに添加剤としてシクロヘキンルアミンを0.
1重量%添加した液晶(メルク社製、商品名ZL136
54)を注入した。このようにして完成した強誘電性液
晶セルは、配向ムラのない良好な配向状態を示し、電圧
印加により、双安定性が保持された良好な電気光学特性
が得られ、さらに長期間にわたり双安定性が保持された
(Example 17) Using N-alkoxymethyl modified nylon, Example 1
4 and Example 15 to which 0.0.0.
Liquid crystal containing 1% by weight (manufactured by Merck & Co., trade name: ZL136)
54) was injected. The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness, and when a voltage is applied, good electro-optical properties that maintain bistability are obtained, and it is also bistable for a long period of time. gender was preserved.

(実施例1日) N−アルコキシメチル変性ナイロンを用いて、実施例1
4および実施例15と同様の操作により作製した強誘電
性液晶セルに添加剤としてベンジルアミンを0.3重量
%添加した液晶(メルク社製。
(Example 1 day) Using N-alkoxymethyl modified nylon, Example 1
4 and Example 15 to which 0.3% by weight of benzylamine was added as an additive to a ferroelectric liquid crystal cell (manufactured by Merck & Co., Ltd.).

商品名ZLI3654)を注入した。このようにして完
成した強誘電性液晶セルは、配向ムラのない良好な配向
状態を示し、電圧印加により、双安定性が保持された良
好な電気光学特性が得られ、さらに長期間にわたり双安
定性が保持された。
(trade name: ZLI3654) was injected. The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness, and when a voltage is applied, good electro-optical properties that maintain bistability are obtained, and it is also bistable for a long period of time. gender was preserved.

(実施例19) N−アルコキシメチル変性ナイロンを用いて、実施例1
4および実施例15と同様の操作により作製した強誘電
性液晶セルに添加剤として分子量400のポリオキシプ
ロピレンジアミンを0.1!量%添加した液晶(メルク
社製、商品名ZL I 3654)を注入した。このよ
うにして完成した強誘電性液晶セルは、配向ムラのない
良好な配向状態を示し、電圧印加により、双安定性が保
持された良好な電気光学特性が得られ、さらに長期間に
わたり双安定性が保持された。
(Example 19) Using N-alkoxymethyl modified nylon, Example 1
4 and Example 15, 0.1! of polyoxypropylene diamine with a molecular weight of 400 was added as an additive to a ferroelectric liquid crystal cell prepared by the same procedure as in Example 15. A liquid crystal (manufactured by Merck & Co., trade name: ZL I 3654) was injected. The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness, and when a voltage is applied, good electro-optical properties that maintain bistability are obtained, and it is also bistable for a long period of time. gender was preserved.

(実施例20) N−アルコキシメチル変性ナイロンを用いて、実施例1
4および実施例15と同様の操作により作成した強誘電
性液晶セルに添加剤として分子量230のポリオキシプ
ロピレンジアミンを0.3重量%添加した液晶(メルク
社製、商品名ZLI3654)を注入した。このように
して完成した強誘電性液晶セルは、配向ムラのUい良好
な配向状態を示し、電圧印加により、双安定性の確保さ
れた良好な電気光学特性が得られ、さらに長期間にわた
り双安定性が保持された。
(Example 20) Using N-alkoxymethyl modified nylon, Example 1
A liquid crystal (manufactured by Merck & Co., trade name: ZLI3654) containing 0.3% by weight of polyoxypropylene diamine having a molecular weight of 230 as an additive was injected into a ferroelectric liquid crystal cell prepared in the same manner as in Example 4 and Example 15. The ferroelectric liquid crystal cell completed in this way exhibits a good alignment state with no alignment unevenness, and when a voltage is applied, good electro-optical properties with ensured bistability are obtained, and furthermore, it can remain stable for a long period of time. Stability was maintained.

(比較例1〕 市販のボリアミンクM(日照化学社製 RN715)を専用のシンナで希釈し、1.5重量%の
ポリアミック酸の溶液を調整した。その後、実施例1と
同様の条件で回転塗布を行ないITOパターンの形成し
たガラス基板上にポリアミック酸の塗膜を形成した。膜
厚は30nmであった。
(Comparative Example 1) Commercially available Boria Mink M (RN715, manufactured by Nichijo Kagaku Co., Ltd.) was diluted with a special thinner to prepare a 1.5% by weight polyamic acid solution. Thereafter, spin coating was performed under the same conditions as in Example 1. A coating film of polyamic acid was formed on the glass substrate on which the ITO pattern was formed.The film thickness was 30 nm.

以下実施例工および実施例2と同様の操作により、作製
した強誘電性液晶セルはツイスト配向状態を(比較例2
) 市販のポリアミック酸(日照化学社製 RN715)を専用のシンナで希釈し、3.0重量%の
ポリアミック酸の溶液を調整した。その後、実施例1七
同様の条件で回転塗布を行ない[TOパターンの形成し
たガラス基板上にポリアミック酸の塗膜を形成した。W
4厚は50nmであった。
In the following, the fabricated ferroelectric liquid crystal cell was subjected to the same operations as in Example 2 and Example 2, and the twisted alignment state (Comparative Example 2) was obtained.
) A commercially available polyamic acid (RN715, manufactured by Nissei Kagaku Co., Ltd.) was diluted with a special thinner to prepare a 3.0% by weight polyamic acid solution. Thereafter, spin coating was performed under the same conditions as Example 17 [A coating film of polyamic acid was formed on the glass substrate on which the TO pattern was formed. W
4 thickness was 50 nm.

以下実施例1および実施例2と同様の操作により、作製
した強誘電性液晶セルはツイスト配向状態を示し、電圧
印加後も双安定性は実現しなかった。
The ferroelectric liquid crystal cell produced by the same operations as in Examples 1 and 2 showed a twisted alignment state and did not achieve bistability even after voltage application.

(比較例3) 市販のボリアミンク#(日照化学社製 SE4110)を専用のシンナで希釈し、1.5重量%
のポリアミック酸の溶液を調製した。その後、実施例1
と同様の条件で回転塗布を行ないITOパターンの形成
したガラス基板上にポリアミック酸の塗膜を形成した。
(Comparative Example 3) Commercially available Boria Mink # (SE4110 manufactured by Nissei Kagaku Co., Ltd.) was diluted with a special thinner to 1.5% by weight.
A solution of polyamic acid was prepared. After that, Example 1
A coating film of polyamic acid was formed on a glass substrate on which an ITO pattern was formed by spin coating under the same conditions as described above.

膜厚は30nmであった。The film thickness was 30 nm.

以下具体的実施例1および具体的実施例2と同様の操作
により、作製した強誘電性液晶セルはツイスト配向状態
を示し、電圧印加後も双安定性は実現しなかった。
The ferroelectric liquid crystal cell produced by the same operations as in Specific Example 1 and Specific Example 2 showed a twisted alignment state, and did not realize bistability even after voltage application.

(比較例4) 市販のポリアミック#(日照化学社製 S’E4210)を専用のシンナで希釈し、1,5重量
%のポリアミック酸の溶液を調製した。その後、実施例
1と同様の条件で回転塗布を行ない■TOパターンの形
成したガラス基板上にポリアミック酸の!!!膜を形成
した。膜厚は50nmであった。
(Comparative Example 4) Commercially available polyamic # (S'E4210, manufactured by Nissei Kagaku Co., Ltd.) was diluted with a special thinner to prepare a 1.5% by weight polyamic acid solution. Thereafter, spin coating was performed under the same conditions as in Example 1 to coat the glass substrate on which the TO pattern was formed. ! ! A film was formed. The film thickness was 50 nm.

以下実施例1および実施例2と同様の操作により、作製
した強誘電性液晶セルはツイスト配向状態を示し、電圧
印加後も双安定性は実現しなかった。
The ferroelectric liquid crystal cell produced by the same operations as in Examples 1 and 2 showed a twisted alignment state and did not achieve bistability even after voltage application.

(比較例5) 1.5gのN−アルコキシメチル変性ナイロンを98.
5gのメチルアルコール %のN−アルコキシメチル変性ナイロンのメタノール溶
液を調製した.その後、実施例14と同様の条件で回転
塗布を行ないITOパターンの形成したガラス基板上に
N−アルコキシメチル変性ナイロンの塗膜を形成した.
膜厚は30nmであった.以下実施例14および実施例
15と同様の操作により、作製した強誘電性液晶セルは
ツイスト配向状態を示し、電圧印加後も双安定性は実現
しなかった。
(Comparative Example 5) 1.5 g of N-alkoxymethyl modified nylon was heated to 98.
A methanol solution of 5 g of N-alkoxymethyl modified nylon with % methyl alcohol was prepared. Thereafter, spin coating was performed under the same conditions as in Example 14 to form a coating film of N-alkoxymethyl-modified nylon on the glass substrate on which the ITO pattern had been formed.
The film thickness was 30 nm. The ferroelectric liquid crystal cell produced by the same operations as in Examples 14 and 15 showed a twisted alignment state and did not achieve bistability even after voltage application.

(比較例6) 3.0gのN−アルコキシメチル変性ナイロンを97.
0gのメチルアルコールに溶かし、3.0重量%のN−
アルコキシメチル変性ナイロンのメタノール溶液を調製
した。その後、実施例14と同様の条件で回転塗布を行
ないITOパターンの形成したガラス基板上にポリアミ
ック酸の塗膜を形成した。膜厚は50nmであった。以
下実施例14および実施例15と同様の操作により、作
製した強誘電性液晶セルはツイスト配向状態を示し、電
圧印加後も双安定性は実現しなかった。
(Comparative Example 6) 3.0g of N-alkoxymethyl modified nylon was heated to 97.0g.
Dissolved in 0g of methyl alcohol, 3.0% by weight of N-
A methanol solution of alkoxymethyl-modified nylon was prepared. Thereafter, spin coating was performed under the same conditions as in Example 14 to form a polyamic acid coating film on the glass substrate on which the ITO pattern was formed. The film thickness was 50 nm. The ferroelectric liquid crystal cell produced by the same operations as in Examples 14 and 15 showed a twisted alignment state and did not achieve bistability even after voltage application.

なお、以上の実施例および比較例において、ポリアミド
配向制御膜として全芳香族系のポリアミック酸(日照化
学社製、商品名RN715およびSE4110)および
アルコール可溶性のN−アルコキシメチル変性ナイロン
を用いたが、ポリアミド配向制御膜としてナイロン(ナ
イロン6、ナイロン66)を用いた場合も同様の結果が
得られた。
In the above Examples and Comparative Examples, fully aromatic polyamic acid (manufactured by Nissho Kagaku Co., Ltd., product names RN715 and SE4110) and alcohol-soluble N-alkoxymethyl-modified nylon were used as the polyamide orientation control film. Similar results were obtained when nylon (nylon 6, nylon 66) was used as the polyamide orientation control film.

また、以上の実施例および比較例においては、ポリイミ
ドの膜を直接透明電極上に形成し、ラビングしたが、本
発明は透明電極上に短絡防止のために形成する酸化珪素
などの上に形成したポリアミドの表面をラビングした場
合にも適用できる。
In addition, in the above Examples and Comparative Examples, a polyimide film was formed directly on a transparent electrode and rubbed, but in the present invention, a polyimide film was formed on a silicon oxide film formed on a transparent electrode to prevent short circuits. It can also be applied when the surface of polyamide is rubbed.

発明の効果 以上のように本発明はポリアミック酸の塗膜に配向処理
を施し液晶配向制御膜とし、その膜厚を0.5nm〜2
0nmにすることで強誘電性液晶分子の配向を制御する
ことが可能になる。また、これを液晶素子に応用した場
合には、素子の全面にわたって均一な配向を容易に低コ
ストで実現でき、色調の優れた大型のカラー液晶表示装
置を提供できるという効果が得られる。
Effects of the Invention As described above, the present invention subjects a coating film of polyamic acid to an alignment treatment to form a liquid crystal alignment control film, and the film thickness is 0.5 nm to 2.0 nm.
Setting the thickness to 0 nm makes it possible to control the orientation of ferroelectric liquid crystal molecules. Furthermore, when this is applied to a liquid crystal element, uniform alignment can be easily achieved over the entire surface of the element at low cost, and a large color liquid crystal display device with excellent color tone can be provided.

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

第1図は本発明の一実施例の液晶素子の断面図、第2図
は同平面図である。 11・・・・・・基板、12・・・・・・透明電極層、
1・3・・・・・・配向制御膜、14・・・・・・スペ
ーサ兼シール樹脂、15・・・液晶支持板、16・・・
・・・液晶、21・・・・・・上側液晶支持体、22・
・・・・・下側液晶支持板、23・・・・・・上側液晶
支持板のラビング処理方向、24・・・・・・下側液晶
支持板のラビング処理方向、25・・・・・・スペーサ
兼シール樹脂。 代理人の氏名 弁理士 粟野重量 はか1名+1−一暮
、駈 12−旌明を漬1 +5−−−Jt晶む中抜 IG−戒み 1E;
FIG. 1 is a sectional view of a liquid crystal element according to an embodiment of the present invention, and FIG. 2 is a plan view thereof. 11...Substrate, 12...Transparent electrode layer,
1.3...Alignment control film, 14...Spacer/sealing resin, 15...Liquid crystal support plate, 16...
...Liquid crystal, 21... Upper liquid crystal support, 22.
...Lower liquid crystal support plate, 23...Rubbing direction of upper liquid crystal support plate, 24...Rubbing direction of lower liquid crystal support plate, 25...・Spacer and seal resin. Name of agent: Patent attorney Shigeki Awano Haka 1 person + 1 - Ikukure, Katsu 12 - Jimei wo Tsuke 1 + 5 --- Jt Akimu Nakanuki IG - Commandments 1E;

Claims (3)

【特許請求の範囲】[Claims] (1)少なくとも一方の基板上に、膜厚が0.5nm〜
20.0nmで配向処理をうけたポリアミドの塗膜を有
する一対の対向する液晶支持板の間隙中に強誘電性液晶
物質を保持する強誘電性液晶素子。
(1) Film thickness of 0.5 nm or more on at least one substrate
A ferroelectric liquid crystal element having a ferroelectric liquid crystal material held in a gap between a pair of opposing liquid crystal support plates having a coating of polyamide subjected to an orientation treatment at 20.0 nm.
(2)対向する液晶支持板の間隙中に保持する液晶物質
がピリミジン系の液晶であって、かつ強誘電性を示す請
求項(1)記載の強誘電性液晶素子。
(2) The ferroelectric liquid crystal element according to claim 1, wherein the liquid crystal substance held in the gap between the opposing liquid crystal support plates is a pyrimidine liquid crystal and exhibits ferroelectricity.
(3)対向する液晶支持板の間隙中に保持する液晶物質
に添加物としてアミン化合物を加えた請求項(1)記載
の強誘電性液晶素子。
(3) The ferroelectric liquid crystal element according to claim (1), wherein an amine compound is added as an additive to the liquid crystal material held in the gap between the opposing liquid crystal support plates.
JP15194790A 1990-06-11 1990-06-11 Ferroelectric liquid crystal element Pending JPH0443325A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15194790A JPH0443325A (en) 1990-06-11 1990-06-11 Ferroelectric liquid crystal element

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15194790A JPH0443325A (en) 1990-06-11 1990-06-11 Ferroelectric liquid crystal element

Publications (1)

Publication Number Publication Date
JPH0443325A true JPH0443325A (en) 1992-02-13

Family

ID=15529684

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15194790A Pending JPH0443325A (en) 1990-06-11 1990-06-11 Ferroelectric liquid crystal element

Country Status (1)

Country Link
JP (1) JPH0443325A (en)

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