JPH037913A - Liquid crystal oriented film and production thereof and liquid crystal display device using this film - Google Patents

Liquid crystal oriented film and production thereof and liquid crystal display device using this film

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Publication number
JPH037913A
JPH037913A JP34065689A JP34065689A JPH037913A JP H037913 A JPH037913 A JP H037913A JP 34065689 A JP34065689 A JP 34065689A JP 34065689 A JP34065689 A JP 34065689A JP H037913 A JPH037913 A JP H037913A
Authority
JP
Japan
Prior art keywords
liquid crystal
alignment film
silane surfactant
carbon chain
silane
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.)
Granted
Application number
JP34065689A
Other languages
Japanese (ja)
Other versions
JP2558903B2 (en
Inventor
Kazufumi Ogawa
一文 小川
Norihisa Mino
規央 美濃
Hideji Tamura
田村 秀治
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
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Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP1340656A priority Critical patent/JP2558903B2/en
Publication of JPH037913A publication Critical patent/JPH037913A/en
Application granted granted Critical
Publication of JP2558903B2 publication Critical patent/JP2558903B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nanotechnology (AREA)
  • Physics & Mathematics (AREA)
  • Composite Materials (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Materials Engineering (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Liquid Crystal (AREA)

Abstract

PURPOSE:To obtain the oriented film which has high performance and is uniform and thin by using a monomolecular film chemically adsorbed and formed with a specific silane surfactant. CONSTITUTION:The oriented film which has the high performance and is uniform and thin is obtd. if the monomolecular film 2 chemically adsorbed and formed with the silane surfactant having long carbon chains 3 and short carbon chains 4 of a straight chain form directly on an electrode or indirectly via an arbitrary thin film is used as the oriented film.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は 液晶を用いた画像表示装置およびその製造方
法に関するものであム さらに詳しくζ上 TV両画像コンピュータ画像等を表
示する液晶を用いた平面表示パネルに用いる液晶配向膜
およびその製造方法およびそれを用いた液晶表示装置と
その製造方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to an image display device using a liquid crystal and a method for manufacturing the same. The present invention relates to a liquid crystal alignment film used in a panel, a method for manufacturing the same, a liquid crystal display device using the same, and a method for manufacturing the same.

従来の技術 従来カラー液晶表示パネル(表 マトリックス状に配置
された対向電極を形成した2つの基板の間にポリビニル
アルコールやポリイミドをスピナーで塗布した後ラビン
グした液晶配向膜を介して液晶を封入した装置が一般的
であっ九 例え(瓜 第8図に示すようへ 手取 第1のガラス基
板31上に画素電極32を持ったTFTアレイ33を形
成したものと、第2のガラス基板34上に複数個の赤青
緑のカラーフィルター35が形成さ扛 さらにその上に
共通透明電極36が形成されたもののそれぞれに ポリ
ビニルアルコールやポリイミドをスピナーを用いて回転
塗布形成L ラビングを行ない液晶配向膜37を形成ヒ
スペーサ−38を介して対向して接着剤39で接着し組
み立てた徽 ツイストネマチック(TN)液晶40等を
注入しパネル構造を形成した徹 パネルの裏表に偏光板
41.42を設置し バックライト43を照射しなが6
  TPTを動作させ矢Ell Aの方向にカラー画像
を表示する構造であa発明が解決しようとする課題 しかしなが収 従来の配向膜の作成(上 ポリビニルア
ルコールやポリイミドを有機溶媒に溶解させ回転塗布法
などを用いて塗布形成した後、フェルト布等を用いてラ
ビングを行なう方法が用いられていたたべ 大面積パネ
ル(例えば14インチデイスプレィ)では配向膜の均一
コーティングが難しいという課題があっ九 まt、:、回転塗布では塗布厚が数ミクロン程度にもな
り、強誘電液晶のような1000オングストローム程度
の厚みの配向膜を必要とする表示パネルで(瓜 性能が
大幅に低減されるという大きな欠点があっ九 本発明(上 大面積パネルにも容易に均一形成でき、か
つ極めて薄い配向膜と、その製造1去 その配向膜を用
いた液晶表示装置及びその製造方法を提供することを目
的とすム 課題を解決するための手段 本発明(よ 直鎖状の炭素鎖を有するシラン系界面活性
剤が、 電極上に直接又は任意の薄膜を介して間接的に
化学吸着して形成された単分子膜を用いた液晶配向膜お
よびその製造方法で、従来の課題を解決したものであ翫 イ乍用 液晶表示装置に使用される配向膜に化学吸着法を用いる
ことにより、高能率で均一かつ薄い配向膜を作成できも 実施例 以上 実施例を第1〜7図を用いて説明すも第1図に示
すようへ 例えばガラスや石英等の親水性の基板1をよ
く乾燥した眞 直接表面に化学吸着法により全面シラン
界面活性剤を吸着反応させて、シラン界面活性剤よりな
る単分子吸着膜2を形成すも (第1図東 R1、R2
は置換基を示すが11でもよい) 即ち例えば第1図に示したような配向Mlよ 以下のよ
うにして製造されも シラン界面活性剤として直鎖状の長い炭素5J13、例
えばR+−(CH2)n −3iC1s (nは整数で
10〜25程度が最も扱い易く、配向効果も大きい)を
持つと、直鎖状の短い炭素鎖4、例えばRz −(CH
a )* −3iC1s (tnは整数で、例えばnが
10〜25の場合にはmは1〜5カ(配向効果が太き(
〜 またnとのとの差は5以上が望ましくNo)を持2
とを、例えば1:2に混合して用い(な耘 直鎖状の長
い炭素鎖と、短い炭素鎖のシラン系界面活性剤との混合
比i1 1:O〜1:10の範囲がか適当であム )、
2X 10−3〜5x 10−”mol/l程度の濃度
で溶かした80%n−ヘキサデカン、12%四塩化炭魚
 8%クロロホルム溶液を調整し 前記基板1を浸漬す
ム このとき、前記基板lは表面が親水性であり、表面には
一〇H基が含まれていも 従って、−3iCh基と一〇
 〇が脱塩酸反応して 〇− 活性剤による単分子吸着膜2が基板表面に1層形成され
 その厚みは例えば10〜30A程度であも即板 基板
表面に発水性の長さの異なる直鎖状の炭素鎖で、特定の
比率で並んだ状態の単分子膜2が形成されも 従って、この様な配向膜の形成された基板に液晶が接す
ると、第2図に示すように液晶5の分子(上 単分子吸
着膜の長い炭素鎖3aの間隙に入り込み、全体として液
晶の配向が制御されも なおここで3a及び4af友 
第1図における長い炭素t113と短い炭素鎖4をそれ
ぞれ模式的に示したものであム なお、化学吸着用の材料としてlet、  −OH基に
対して結合性を有する基(例えばモノクロロシラン基(
−5iC1基)等)を含んでいれば 実施例で示したシ
ラン系界面活性剤に限定されるものではなしも例えよ 
直鎖状の炭素鎖の一部にF(フッ素)を含むシラン界面
活性剋 例えばCF* −(CHt )。−3iCh輸
は整数で10〜25程度が最も扱いやすい)、またはC
F3−(CF2)++(CH2)n−3iC1s (m
、 nは整数で、合計か10〜25が最も扱い易しモ)
等を用いてk 単分子吸着膜を製造できも また 直鎖状の長い炭素鎖の一部が任意の置換基(R+
)で、他の一端がトリクロロシラン基のシラン系界面活
性剤と、直鎖状の短い炭素鎖の一部か任意の置換基(R
2)で、他の一端がトリクロロシラン基のシラン系界面
活性剤を所定の比率で混合し 吸着形成を行えば配向特
性を変化させることも可能である。
Conventional technology Conventional color liquid crystal display panel (Table 1) A device in which polyvinyl alcohol or polyimide is coated with a spinner between two substrates with opposing electrodes arranged in a matrix, and then liquid crystal is sealed through a liquid crystal alignment film that is rubbed. For example, as shown in FIG. Red, blue, and green color filters 35 are formed.Furthermore, a common transparent electrode 36 is formed on each of them. Polyvinyl alcohol or polyimide is spin-coated using a spinner, and rubbed to form a liquid crystal alignment film 37.His spacer Polarizing plates 41 and 42 are installed on the back and front of the panel, and a backlight 43 is installed on the back and front of the panel. Irradiation Shinaga 6
The problem that the invention aims to solve is to create a structure that displays a color image in the direction of the arrow Ell A by operating the TPT.Creating a conventional alignment film (Part 1) Dissolving polyvinyl alcohol or polyimide in an organic solvent and spinning coating For large-area panels (for example, 14-inch displays), it is difficult to uniformly coat the alignment film. t:, With spin coating, the coating thickness can be as large as several microns, which is a major drawback in that the performance is significantly reduced in display panels such as ferroelectric liquid crystals that require an alignment film approximately 1000 angstroms thick. An object of the present invention is to provide an extremely thin alignment film that can be easily and uniformly formed even on a large-area panel, a liquid crystal display device using the alignment film, and a method for manufacturing the same. Means for Solving the Problems of the Present Invention (1) A single molecule formed by chemically adsorbing a silane surfactant having a linear carbon chain onto an electrode directly or indirectly through an arbitrary thin film. This is a liquid crystal alignment film using a film and its manufacturing method, which solves the conventional problems.By using a chemical adsorption method for the alignment film used in digital liquid crystal display devices, it is possible to produce a highly efficient, uniform and thin film. Although the alignment film can be created, the example is explained using Figs. 1 to 7, but as shown in Fig. A monomolecular adsorption film 2 made of the silane surfactant is formed by adsorbing and reacting the silane surfactant on the entire surface using an adsorption method (Fig. 1 East R1, R2).
indicates a substituent, but may also be 11) That is, for example, from the orientation Ml as shown in FIG. When n −3iC1s (n is an integer of about 10 to 25 is easiest to handle and has a large orientation effect), a short linear carbon chain 4, for example Rz −(CH
a ) * -3iC1s (tn is an integer, for example, when n is 10 to 25, m is 1 to 5 (the orientation effect is thick (
~ Also, the difference between n and 2 is preferably 5 or more.
For example, a mixing ratio of a long straight carbon chain and a silane surfactant with a short carbon chain is preferably in the range of 1:0 to 1:10. Deam),
Prepare a solution of 80% n-hexadecane, 12% carbon tetrachloride, and 8% chloroform dissolved at a concentration of 2X 10-3 to 5x 10-'' mol/l, and immerse the substrate 1 in the solution. has a hydrophilic surface, and even though the surface contains 10H groups, -3iCh groups and 100 react with dehydrochloric acid, forming a monomolecular adsorption film 2 of the activator on the substrate surface. A monomolecular film 2 is formed on the surface of the substrate, with water-repellent linear carbon chains of different lengths arranged in a specific ratio. Therefore, when a liquid crystal comes into contact with a substrate on which such an alignment film is formed, as shown in FIG. is controlled, but here 3a and 4af friends
The long carbon t113 and the short carbon chain 4 in FIG.
-5iC1 group) etc.), it is not limited to the silane surfactants shown in the examples.
Silane surfactants containing F (fluorine) in a part of the linear carbon chain, such as CF*-(CHt). -3iCh import is an integer of 10 to 25, which is easiest to handle), or C
F3-(CF2)++(CH2)n-3iC1s (m
, n is an integer, the sum or 10 to 25 is easiest to handle)
It is also possible to produce a monomolecular adsorption film using, for example, a monomolecular adsorption film of k.
), a silane surfactant whose other end is a trichlorosilane group, and a part of a short linear carbon chain or an arbitrary substituent (R
In 2), it is also possible to change the orientation characteristics by mixing a silane surfactant whose other end is a trichlorosilane group at a predetermined ratio and performing adsorption formation.

ここで上述した任意の置換基R+もしくはR2として(
上 例えば水嵩 ビニル基 メチルエチニル基寛 液晶
分子の配向を妨げない置換基であれば何れでもよし℃ また第3図に示したようへ 封入する液晶2同じ液晶分
子(例えばネマティック液晶部6)を、置換基の一部に
結合したシラン系界面活性剤と、短い炭素鎖を持つシラ
ン系界面活性剤とを所定の比率で混合し 吸着形成を行
え(瓜 封入する特定の液晶に対して特に配向特性の優
れた配向膜が得られも (第3回虫 R*(!  通常
炭化水素鎖の置換基を示すがHでもよい) 従って第4図に示したよう#ζ この様なネマティック
液晶部6aを持つ配向膜の形成された基板にネマティッ
ク液晶7が接すると、ネマティック液晶7の分子は単分
子吸着膜のネマティック液晶部6aの間隙に入り込み、
全体として液晶の配向角度か極めてよく制御されも な
おここで6a及びJal&  第3図におけるネマティ
ック液晶部6と短い炭素鎖4をそれぞれ模式的に示した
ものであム さらにまた第5図に示したよう圏 封入する液晶分子が
強誘電液晶である場合(上 強誘電液晶部8が結合した
シラン系界面活性剤と、短い炭素鎖を持つシラン系界面
活性剤とを所定の比率で吸着形成ずれば 単分子吸着膜
の配向膜を作成できムな敷 強誘電液晶としては アゾ
メチンム アゾギシ系またはエステル系の何れかを用い
ることが出来も またこの場合にk この様な強誘電液晶部8を持つ配向
膜の形成された基板に強誘電液晶が接すると、第6図に
示すように強誘電液晶9の分子(電車分子吸着膜の強誘
電液晶部8aの間隙に入り込へ 全体として液晶の配向
性が極めてよく制御されも なお、ここで、8a及び4
a(友 第5図における強誘電液晶部8と短い炭素鎖4
とをそれぞれ模式的に示したものであも な耘 以上の実施例では最も代表的なものとして、所定
の比率で混合された複数種のシラン系界面活性剤を同時
に化学吸着させた液晶配向膜の伊(および液晶分子を結
合したシラン系界面活性剤と、短い炭素鎖を持つシラン
系界面活性剤とが、 所定の比率で吸着形成されている
単分子膜よりなる液晶配向膜の例を示したが、 直鎖状
の炭素鎖を含むシラン系界面活性剤のみで液晶配向膜を
吸着作成した場合に(友 前記液晶をほぼ垂直に配向さ
せることができる液晶配向膜を作成できた さら凶 この様な配向膜を用いて、液晶表示装置を製造
する場合、第7図に示した一例に基づき説明すも あらかじめマトリックス状に載置された第1の電極群1
1と、この電極を駆動するトランジスター群12を有す
る第1の基板13上と、第1の電極群と対向するように
カラーフィルター群14と、第2の電極15を載置した
第2の基板16上とを用意すム これら基板13と基板16をそれぞれシラン系界面活性
剤を存する非水系の有機溶媒中(例えば「l−パラフィ
ンを用いれば 長い分子の配向を効率よく制御すること
が出来 特にn−ヘキサデカン(よ その効果が著しL
s  )に浸漬し シラン系界面活性剤を化学吸着させ
、それぞれの基板表面に直接前記活性剤のシリコンと前
記基板表面の自然酸化膜とを化学結合させて、液晶配向
膜用の単分子をそれぞれ各1層づつ形成すも なお基板13及び基板16の表面に例えば5L02等の
薄膜を、例えばCVD法やスパッタ法を用いて形成して
用いてもよく、また例えばポリビニルアルコール ゼラ
チン等の親水性の高分子を塗布して用いてもよ賎 シラン系界面活性剤を化学結合させた第1の基板13と
第2の基板16とを、それぞれ電極が対抗するように位
置合わせして、互いの基板にスペーサ−18で間隙を設
け、接着剤19で固定すもこのようにして形成された間
隙&へ 所定の液晶20を注入すム その後、偏光板21、22を組み合わせて完成する。
Here, as any substituent R+ or R2 mentioned above (
For example, water bulk, vinyl group, methyl ethynyl group, any substituent that does not interfere with the alignment of liquid crystal molecules.C Also, as shown in Figure 3, the same liquid crystal molecules (for example, nematic liquid crystal part 6) of the liquid crystal 2 to be encapsulated are substituted. A silane surfactant bonded to a part of the group and a silane surfactant with a short carbon chain are mixed in a predetermined ratio to form an adsorbent. Even if an excellent alignment film is obtained (3rd roundworm R* (! Usually indicates a substituent on a hydrocarbon chain, but H may also be used), #ζ as shown in FIG. When the nematic liquid crystal 7 comes into contact with the substrate on which the film is formed, the molecules of the nematic liquid crystal 7 enter the gaps between the nematic liquid crystal parts 6a of the monomolecular adsorption film.
As a whole, the orientation angle of the liquid crystal is very well controlled.The nematic liquid crystal part 6 and the short carbon chain 4 in FIG. 3 are schematically shown in FIG. When the liquid crystal molecules to be enclosed are ferroelectric liquid crystals (above), if the silane surfactant to which the ferroelectric liquid crystal part 8 is bonded and the silane surfactant having a short carbon chain are adsorbed and formed in a predetermined ratio. In this case, it is also possible to use either azomethine, azomethine, or ester as the ferroelectric liquid crystal. When the ferroelectric liquid crystal comes into contact with the substrate on which the ferroelectric liquid crystal is formed, as shown in FIG. Note that here, 8a and 4
a (Friend) Ferroelectric liquid crystal part 8 and short carbon chain 4 in Figure 5
In the above examples, the most typical one is a liquid crystal alignment film in which multiple types of silane surfactants mixed at a predetermined ratio are simultaneously chemically adsorbed. An example of a liquid crystal alignment film consisting of a monomolecular film in which a silane surfactant bonded with liquid crystal molecules and a silane surfactant with a short carbon chain are adsorbed and formed in a predetermined ratio is shown below. However, when a liquid crystal alignment film was adsorbed and created using only a silane surfactant containing linear carbon chains, it was possible to create a liquid crystal alignment film that could align the liquid crystals almost vertically. When manufacturing a liquid crystal display device using an alignment film such as
1, a first substrate 13 having a transistor group 12 for driving this electrode, and a second substrate having a color filter group 14 and a second electrode 15 placed so as to face the first electrode group. The substrates 13 and 16 are prepared in a non-aqueous organic solvent containing a silane surfactant (for example, if l-paraffin is used, the orientation of long molecules can be efficiently controlled. n-hexadecane (which has a remarkable effect)
s) to chemically adsorb a silane-based surfactant, and chemically bond the active agent silicon and the natural oxide film on the substrate surface directly to the surface of each substrate to form a single molecule for the liquid crystal alignment film. Alternatively, a thin film such as 5L02 may be formed on the surface of the substrate 13 and the substrate 16 by using a CVD method or a sputtering method. A first substrate 13 and a second substrate 16, each coated with a polymer and chemically bonded with a silane-based surfactant, are aligned so that their electrodes face each other. A gap is provided with a spacer 18, and a predetermined liquid crystal 20 is injected into the gap thus formed and fixed with an adhesive 19. Thereafter, the polarizing plates 21 and 22 are assembled to complete the process.

この様なデバイスで(友 バックライト23全面に照射
しなか収 ビデオ信号を用いて各々のトランジスタを駆
動すれ(′L 矢印Aの方向に映像を表示できも なお本発明によれば 配向膜の製造工程でラビングは必
ずしも必要ではないが、ラビングを行っても良いことは
勿論であム 発明の効果 以上述べてきた方法(よ 液晶配向膜の製造置型極表面
に直接シラン界面活性剤を単分子状に1層化学吸着させ
る方法を用いているたべ 高能率で均一かつ薄く作成で
きる効果があ翫 さらに 吸着形成された配向膜ζ瓜 特定の液晶例えば
ネマティック液晶や強誘電液晶を結合させることが可能
なた八 極めて配向制御性がよ(℃また 液晶と電極の
間に挟まれる絶縁性の膜としては極めて薄いので、液晶
表示装置の駆動エネルギーを少なく出来る効果もあム なお本発明の方法を用いた配向膜 及びこの配向膜を用
いた液晶セルで(友 分子内ダイポールの大きな分子を
特定の方向に向きをそろえて並べることができるので、
極めて大きな2次非線形光学効果を発現させることも可
能とな翫
Even if such a device can display an image in the direction of arrow A without illuminating the entire backlight 23 and driving each transistor using a video signal, according to the present invention, it is still possible to produce an alignment film. Although rubbing is not necessarily required in the process, it is of course possible to perform rubbing. Using a single-layer chemical adsorption method, it is possible to create a uniform and thin layer with high efficiency.Furthermore, the adsorbed alignment film can be used to bond specific liquid crystals, such as nematic liquid crystals and ferroelectric liquid crystals. Furthermore, since the insulating film sandwiched between the liquid crystal and the electrode is extremely thin, the method of the present invention has the effect of reducing the driving energy of the liquid crystal display device. With an alignment film and a liquid crystal cell using this alignment film, large intramolecular dipole molecules can be aligned in a specific direction.
It is also possible to produce extremely large second-order nonlinear optical effects.

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

第11i  第3図及び第5図は分子レベルまで拡大し
た概念は 第2巨 第4図及び第6図は液晶を封゛大し
た場合の液晶分子の配向の状態の模式的は 第7図は本
発泡の配向膜を用いた液晶表示デバイスの断面概念は 
第8図従来の配向膜を用いた液晶表示デバイスの断面概
念図を示す。 l・・・基板、 2・・・単分子吸着a  3. 3a
・・・長い炭素坑 4,4a・・・短い炭素lL 5・
・・液a6゜6a・・・ネマチック液晶訊 7・・・ネ
マチック液晶8、8a・・・強誘電液晶区 9・・・強
誘電液晶 17・・・単分子配向膜
11i Figures 3 and 5 show the concept expanded to the molecular level. Figures 4 and 6 show the schematic diagram of the state of orientation of liquid crystal molecules when the liquid crystal is enlarged. The cross-sectional concept of a liquid crystal display device using this foamed alignment film is
FIG. 8 shows a conceptual cross-sectional view of a liquid crystal display device using a conventional alignment film. l...Substrate, 2...Single molecule adsorption a3. 3a
...Long carbon pit 4,4a...Short carbon 1L 5.
...Liquid a6゜6a... Nematic liquid crystal 7... Nematic liquid crystal 8, 8a... Ferroelectric liquid crystal 9... Ferroelectric liquid crystal 17... Monomolecular alignment film

Claims (27)

【特許請求の範囲】[Claims] (1)直鎖状の炭素鎖を持つシラン系界面活性剤が、電
極上に直接または任意の薄膜を介して間接に化学吸着形
成された単分子膜を用いることを特徴とした液晶配向膜
(1) A liquid crystal alignment film characterized by using a monomolecular film in which a silane surfactant having a linear carbon chain is chemically adsorbed directly or indirectly through an arbitrary thin film on an electrode.
(2)直鎖状の炭素鎖を持つシラン系界面活性剤が、長
い炭素鎖を持つシラン系界面活性剤と、短い炭素鎖を持
つシラン系界面活性剤とを、所定の比率で混合されたも
のであることを特徴とした請求項1記載の液晶配向膜。
(2) A silane surfactant with a linear carbon chain is a mixture of a silane surfactant with a long carbon chain and a silane surfactant with a short carbon chain at a predetermined ratio. The liquid crystal alignment film according to claim 1, wherein the liquid crystal alignment film is a liquid crystal alignment film.
(3)長い炭素鎖の炭素数が10〜25であり、短い炭
素鎖の炭素数が1〜5であることを特徴とした、請求項
2記載の液晶配向膜。
(3) The liquid crystal aligning film according to claim 2, wherein the long carbon chain has 10 to 25 carbon atoms, and the short carbon chain has 1 to 5 carbon atoms.
(4)長い炭素鎖の一端が任意の置換基で他の一端がト
リクロロシラン基であるシラン系界面活性剤と、短い炭
素鎖の一端が任意の置換基で他の一端がトリクロロシラ
ン基であるシラン系界面活性剤であることを特徴とした
、請求項2もしくは3何れかに記載の液晶配向膜。
(4) A silane surfactant in which one end of a long carbon chain is an arbitrary substituent and the other end is a trichlorosilane group, and one end of a short carbon chain is an arbitrary substituent and the other end is a trichlorosilane group. The liquid crystal alignment film according to claim 2 or 3, characterized in that it is a silane surfactant.
(5)液晶分子と類似の構造を有する化合物を含むシラ
ン系界面活性剤を、電極上に直接または任意の薄膜を介
して間接に化学吸着形成された単分子膜を用いることを
特徴とした液晶配向膜。
(5) A liquid crystal characterized by using a monomolecular film of a silane surfactant containing a compound having a structure similar to that of liquid crystal molecules, formed on an electrode by chemisorption, either directly or indirectly through an arbitrary thin film. Orientation film.
(6)液晶分子と類似の構造を有する化合物を含むシラ
ン系界面活性剤と、短い直鎖状の炭素鎖を持つシラン系
界面活性剤とを、所定の比率で混合し化学吸着形成され
た単分子膜を用いることを特徴とした 請求項5記載の
液晶配向膜。
(6) A silane surfactant containing a compound with a structure similar to that of liquid crystal molecules and a silane surfactant having a short linear carbon chain are mixed at a predetermined ratio to form chemically adsorbed monomers. The liquid crystal alignment film according to claim 5, characterized in that a molecular film is used.
(7)液晶分子がネマティック液晶であることを特徴と
した、請求項5もしくは6何れかに記載の液晶配向膜。
(7) The liquid crystal alignment film according to claim 5 or 6, wherein the liquid crystal molecules are nematic liquid crystals.
(8)液晶分子が強誘電液晶であることを特徴とした、
請求項5もしくは6何れかに記載の液晶配向膜。
(8) characterized in that the liquid crystal molecules are ferroelectric liquid crystals;
The liquid crystal alignment film according to claim 5 or 6.
(9)強誘電液晶が、アゾメチン系、アゾキシ系または
エステル系の何れかであることを特徴とした、請求項8
記載の液晶配向膜。
(9) Claim 8, wherein the ferroelectric liquid crystal is one of azomethine type, azoxy type, or ester type.
The liquid crystal alignment film described above.
(10)所定の基板表面に直接もしくは任意の薄膜を介
して間接的に 非水系の有機溶媒中でシラン系界面活性
剤または所定の比率で混合された複数種のシラン系界面
活性剤を同時に化学吸着させ、前記基板表面もしくは前
記任意の薄膜に直接前記活性剤のシリコンと前記基板表
面の自然酸化膜とを化学結合させて単分子膜を1層形成
する工程を含むことを特徴とした液晶配向膜の製造方法
(10) Simultaneously chemically coat a silane surfactant or multiple types of silane surfactants mixed at a predetermined ratio in a nonaqueous organic solvent directly or indirectly on the surface of a predetermined substrate. Liquid crystal alignment characterized by comprising a step of adsorbing and chemically bonding silicon as the activator and a natural oxide film on the surface of the substrate directly to the surface of the substrate or any thin film to form a monolayer. Membrane manufacturing method.
(11)シラン系界面活性剤の一端が、少なくともモノ
クロロシラン基誘導体であることを特徴とした、請求項
10記載の液晶配向膜の製造方法。
(11) The method for producing a liquid crystal aligning film according to claim 10, wherein one end of the silane surfactant is at least a monochlorosilane group derivative.
(12)シラン系界面活性剤の一端が任意の置換基で他
の一端がモノクロロシラン基誘導体であることを特徴と
した、請求項10もしくは11何れかに記載の液晶配向
膜の製造方法。
(12) The method for producing a liquid crystal aligning film according to claim 10 or 11, wherein one end of the silane surfactant is an arbitrary substituent and the other end is a monochlorosilane group derivative.
(13)複数種のシラン系界面活性剤が、長い炭素鎖を
持つシラン系界面活性剤と、短い炭素鎖を持つシラン系
界面活性剤とであることを特徴とした、請求項10記載
の液晶配向膜の製造方法。
(13) The liquid crystal according to claim 10, wherein the plurality of types of silane surfactants are a silane surfactant having a long carbon chain and a silane surfactant having a short carbon chain. A method for producing an alignment film.
(14)長い炭素鎖を有するシラン系界面活性剤と、短
い炭素鎖を有するシラン系界面活性剤との混合比が、1
:0〜1:10であることを特徴とした、請求項13記
載の液晶配向膜の製造方法。
(14) The mixing ratio of the silane surfactant with a long carbon chain and the silane surfactant with a short carbon chain is 1
The method for producing a liquid crystal alignment film according to claim 13, wherein the ratio is 0 to 1:10.
(15)複数種のシラン系界面活性剤が、液晶分子を結
合したシラン系界面活性剤と、短い直鎖状の炭素鎖を持
つシラン系界面活性剤とであることを特徴とした、請求
項10〜12何れかに記載の液晶配向膜の製造方法。
(15) A claim characterized in that the plurality of types of silane surfactants are a silane surfactant bonded to liquid crystal molecules and a silane surfactant having a short linear carbon chain. 13. The method for producing a liquid crystal alignment film according to any one of 10 to 12.
(16)液晶分子の一端にトリクロロシラン基が結合さ
れたシラン系界面活性剤と、短い直鎖状の炭素鎖の一端
が任意の置換基で他の一端がトリクロロシラン基である
シラン系界面活性剤とを用いることを特徴とした、請求
項15記載の液晶配向膜の製造方法。
(16) A silane surfactant in which a trichlorosilane group is bonded to one end of a liquid crystal molecule, and a silane surfactant in which one end of a short linear carbon chain is an arbitrary substituent and the other end is a trichlorosilane group. The method for producing a liquid crystal alignment film according to claim 15, characterized in that the method uses a liquid crystal alignment film.
(17)液晶分子がネマティック液晶であることを特徴
とした、請求項15もしくは16何れかに記載の液晶配
向膜の製造方法。
(17) The method for producing a liquid crystal alignment film according to claim 15 or 16, wherein the liquid crystal molecules are nematic liquid crystals.
(18)液晶分子が強誘電液晶であることを特徴とした
、請求項15もしくは16何れかに記載の液晶配向膜の
製造方法。
(18) The method for producing a liquid crystal alignment film according to claim 15 or 16, wherein the liquid crystal molecules are ferroelectric liquid crystals.
(19)強誘電液晶がアゾメチン系、アゾキシ系または
エステル系の何れかであることを特徴とした、請求項1
8記載の液晶配向膜の製造方法。
(19) Claim 1, characterized in that the ferroelectric liquid crystal is one of azomethine type, azoxy type, or ester type.
8. The method for producing a liquid crystal alignment film according to 8.
(20)非水系溶媒としてn−パラフィンを含むことを
特徴とした特許請求の範囲第10項記載の液晶表示装置
の製造方法。
(20) The method for manufacturing a liquid crystal display device according to claim 10, characterized in that the non-aqueous solvent contains n-paraffin.
(21)n−パラフィンがn−セタンであることを特徴
とした特許請求の範囲第20項記載の液晶表示装置の製
造方法。
(21) The method for manufacturing a liquid crystal display device according to claim 20, wherein the n-paraffin is n-cetane.
(22)シラン系界面活性剤が化学吸着形成された2つ
の対向する単分子膜よりなる液晶配向膜に、液晶が挟ま
れていることを特徴とする、液晶表示装置。
(22) A liquid crystal display device, characterized in that a liquid crystal is sandwiched between liquid crystal alignment films made of two opposing monomolecular films in which a silane surfactant is chemically adsorbed.
(23)シラン系界面活性剤が直鎖状の長い炭素鎖を持
つシラン系界面活性剤と、直鎖状の短い炭素数を持つシ
ラン系界面活性剤とを、所定の比率で混合したものであ
ることを特徴とする、請求項22記載の液晶表示装置。
(23) The silane surfactant is a mixture of a silane surfactant with a long linear carbon chain and a silane surfactant with a short linear carbon number in a predetermined ratio. 23. The liquid crystal display device according to claim 22, characterized in that:
(24)長い炭素鎖が液晶分子であることを特徴とする
、請求項23記載の液晶表示装置。
(24) The liquid crystal display device according to claim 23, wherein the long carbon chain is a liquid crystal molecule.
(25)液晶分子がネマティック液晶であることを特徴
とした請求項24記載の液晶表示装置。
(25) The liquid crystal display device according to claim 24, wherein the liquid crystal molecules are nematic liquid crystals.
(26)液晶分子が強誘電液晶であることを特徴とした
、請求項24記載の液晶表示装置。
(26) The liquid crystal display device according to claim 24, wherein the liquid crystal molecules are ferroelectric liquid crystals.
(27)強誘電液晶がアゾメチン系、アゾキシ系または
エステル系の何れかであることを特徴とした、請求項2
6記載の液晶表示装置。
(27) Claim 2, characterized in that the ferroelectric liquid crystal is one of azomethine type, azoxy type, or ester type.
6. The liquid crystal display device according to 6.
JP1340656A 1989-03-09 1989-12-29 Liquid crystal alignment film, manufacturing method thereof, and liquid crystal display device using the same Expired - Fee Related JP2558903B2 (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08262452A (en) * 1996-04-19 1996-10-11 Matsushita Electric Ind Co Ltd Liquid crystal oriented film, its production and liquid crystal display using the film
EP1132147A2 (en) * 1999-02-10 2001-09-12 Matsushita Electric Industrial Co., Ltd. Organic thin films, process for the production thereof and equipment therefor
US6451392B1 (en) 1999-07-05 2002-09-17 Matsushita Electric Industrial Co., Ltd. Chemical adsorbate compound, organic film, liquid crystal alignment film, and liquid crystal display device utilizing the chemical adsorbate compound
US6495221B1 (en) 1997-07-31 2002-12-17 Matsushita Electric Industrial Co., Ltd. Chemisorptive substance, aligned liquid-crystal film and liquid-crystal display element both made by using the same, and processes for producing these
US6517401B1 (en) 1997-11-18 2003-02-11 Matsushita Electric Industrial Co., Ltd. Process for the production of monomolecular chemisorption film, and processes for the production of liquid crystal alignment films and liquid crystal displays by using the chemisorption film
US6524715B1 (en) 1999-07-05 2003-02-25 Matsushita Electric Industrial Co., Ltd. Thin-film forming chemical adsorption material, producing method thereof and applications thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6097324A (en) * 1983-10-31 1985-05-31 Sharp Corp Manufacture of liquid crystal display element
JPH023017A (en) * 1988-06-20 1990-01-08 Sony Corp Liquid crystal display element

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6097324A (en) * 1983-10-31 1985-05-31 Sharp Corp Manufacture of liquid crystal display element
JPH023017A (en) * 1988-06-20 1990-01-08 Sony Corp Liquid crystal display element

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08262452A (en) * 1996-04-19 1996-10-11 Matsushita Electric Ind Co Ltd Liquid crystal oriented film, its production and liquid crystal display using the film
US6495221B1 (en) 1997-07-31 2002-12-17 Matsushita Electric Industrial Co., Ltd. Chemisorptive substance, aligned liquid-crystal film and liquid-crystal display element both made by using the same, and processes for producing these
US6517401B1 (en) 1997-11-18 2003-02-11 Matsushita Electric Industrial Co., Ltd. Process for the production of monomolecular chemisorption film, and processes for the production of liquid crystal alignment films and liquid crystal displays by using the chemisorption film
EP1132147A2 (en) * 1999-02-10 2001-09-12 Matsushita Electric Industrial Co., Ltd. Organic thin films, process for the production thereof and equipment therefor
US6451392B1 (en) 1999-07-05 2002-09-17 Matsushita Electric Industrial Co., Ltd. Chemical adsorbate compound, organic film, liquid crystal alignment film, and liquid crystal display device utilizing the chemical adsorbate compound
US6524715B1 (en) 1999-07-05 2003-02-25 Matsushita Electric Industrial Co., Ltd. Thin-film forming chemical adsorption material, producing method thereof and applications thereof

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