JP3579921B2 - Manufacturing method of optical anisotropic body - Google Patents
Manufacturing method of optical anisotropic body Download PDFInfo
- Publication number
- JP3579921B2 JP3579921B2 JP15457494A JP15457494A JP3579921B2 JP 3579921 B2 JP3579921 B2 JP 3579921B2 JP 15457494 A JP15457494 A JP 15457494A JP 15457494 A JP15457494 A JP 15457494A JP 3579921 B2 JP3579921 B2 JP 3579921B2
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- substrate
- crystal composition
- polymerizable liquid
- monofunctional
- 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 - Lifetime
Links
- 230000003287 optical effect Effects 0.000 title claims description 28
- 238000004519 manufacturing process Methods 0.000 title claims description 17
- 239000000758 substrate Substances 0.000 claims description 104
- 239000004973 liquid crystal related substance Substances 0.000 claims description 76
- 239000000203 mixture Substances 0.000 claims description 57
- 150000001875 compounds Chemical class 0.000 claims description 20
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 12
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 230000001678 irradiating effect Effects 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 230000001747 exhibiting effect Effects 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
- 239000004988 Nematic liquid crystal Substances 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 2
- 125000005397 methacrylic acid ester group Chemical group 0.000 claims description 2
- 239000011521 glass Substances 0.000 description 17
- 239000012071 phase Substances 0.000 description 10
- -1 aromatic hydroxy compound Chemical class 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 229920000106 Liquid crystal polymer Polymers 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- JQWAHKMIYCERGA-UHFFFAOYSA-N (2-nonanoyloxy-3-octadeca-9,12-dienoyloxypropoxy)-[2-(trimethylazaniumyl)ethyl]phosphinate Chemical compound CCCCCCCCC(=O)OC(COP([O-])(=O)CC[N+](C)(C)C)COC(=O)CCCCCCCC=CCC=CCCCCC JQWAHKMIYCERGA-UHFFFAOYSA-N 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 230000007704 transition Effects 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000011368 organic material Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004990 Smectic liquid crystal Substances 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 238000012719 thermal polymerization Methods 0.000 description 2
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 1
- JIGUICYYOYEXFS-UHFFFAOYSA-N 3-tert-butylbenzene-1,2-diol Chemical compound CC(C)(C)C1=CC=CC(O)=C1O JIGUICYYOYEXFS-UHFFFAOYSA-N 0.000 description 1
- 239000004986 Cholesteric liquid crystals (ChLC) Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 150000008062 acetophenones Chemical class 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Polarising Elements (AREA)
- Liquid Crystal (AREA)
- Liquid Crystal Substances (AREA)
Description
【０００１】
【産業上の利用分野】
本発明は、液晶表示素子の視角依存性を解消又は軽減するために有用な光学異方体及びこれを用いた光学異方性を有する基板の製造方法に関する。
【０００２】
【従来の技術】
液晶ディスプレイ素子の視角依存性を軽減するために、厚み方向の屈折率が面内の屈折率より大きなフィルム（光学異方体）を補償板として用いる手段が知られている（Ｍ．Ａｋａｔｓｕｋａ等、Ｊａｐａｎ Ｄｉｓｐｌａｙ ’８９、３３６項、１９８９年）。このような光学異方体として、液晶性高分子を用いたものが特開平５−２７２３５号公報及び特開平５−３４６７８号公報に開示されている。しかしながら、これらの光学異方体は液晶性高分子の垂直配向構造をガラス状態で固定化しており、液晶性高分子のガラス転移点を越える温度では、配向構造が破壊されてしまうため使用温度がガラス転移点によって制限されるという欠点があった。また高分子液晶の粘度は、低分子液晶の粘度と比較して高く、垂直配向状態を得るのに時間がかかり、生産性が落ちるという欠点もあり、これは大面積の補償板等の光学異方体を得ようとするほど、また液晶性高分子のガラス転移点を高く設計するほど、この欠点は顕在化してしまっていた。
【０００３】
これらの問題を解決するために本発明者等は、室温において液晶性を有する重合性液晶組成物を、垂直配向処理を施した基板間に担持させて垂直配向させた後に、光重合させて製造される光学異方性を有する基板を先に提案した。
【０００４】
しかし、この技術によって均一な垂直配向状態を得るのにかかる時間が短縮されたものの、基板表面に垂直配向処理を施さなければならないという煩わしさがあった。
【０００５】
【発明が解決しようとする課題】
本発明が解決しようとする課題は、重合性液晶組成物を基板面に対して垂直配向させる手段として、従来のような垂直配向処理によらず、より容易に得られる製造方法を提供することにあり、これにより内部に垂直配向構造を有する光学異方体の製造効率をより向上させることにある。
【０００６】
【課題を解決するための手段】
本発明者等は上記課題を解決する手段について鋭意検討した結果、かかる課題が重合性液晶組成物液晶の垂直配向を電圧を印加することによって解決できることを見いだし、本発明を提供するに到った。
【０００７】
即ち、本発明は第１の発明として、（１）導電層を有する第１の透明性基板と、導電性を有する第２の基板の間に重合性液晶組成物を介在させる第１工程、
（２）前記２枚の基板間に電圧を印加しながら、第１の透明性基板の側から光を照射する第２工程、及び
（３）第１の透明性基板及び第２の基板を剥離する第３工程
を有する光学異方体の製造方法を提供する。
【０００８】
また、本発明は第２の発明として、（１）導電層を有する第１の透明性基板と、導電性を有する第２の基板の間に重合性液晶組成物を介在させる第１工程、
（２）前記２枚の基板間に電圧を印加しながら、第１の透明性基板の側から光を照射する第２工程、及び
（３）第２の基板を剥離する第３工程
を有する光学異方性を有する基板の製造方法を提供する。
【０００９】
更に、本発明は第３の発明として、（１）導電層を有する２枚の透明性基板の間に重合性液晶組成物を介在させる第１工程、及び
（２）前記２枚の基板間に電圧を印加しながら、第１の透明性基板の側から光を照射する第２工程
を有する光学異方性を有する基板の製造方法を提供する。
【００１０】
以下、第１の発明、第２の発明及び第３の発明を更に詳細に説明する。
本発明で使用する第１の透明性基板としては、例えば、導電層を有するガラスあるいはプラスチック基板が好ましく、具体的には、ＩＴＯ付きガラス基板、ＩＴＯ付きプラスチック基板を挙げることができる。これらの基板は導電性を有していないガラスあるいはプラスチック基板上に、蒸着、メッキ、印刷等の手段を用いることによって容易に得ることができるが、市販のＩＴＯ付き基板を用いることもできる。
【００１１】
本発明で使用する第２の基板としては、それ自体が導電性を有する基板であれば、透明性を有するものであっても、不透明なものであってもよく、また有機材料、無機材料を問わずに使用することができる。具体的には、無機材料としては、例えば、銅、金、銀、錫、鉛、鉄、ニッケル、アルミニウム、ＩＴＯ（インジウムチンオキサイド）等の金属又は金属酸化物等を挙げることができ、有機材料としては導電性ゴム、導電性プラスチック等を挙げることができる。
【００１２】
本発明で使用する重合性液晶組成物としては、液晶状態での光重合の際の意図しない熱重合の誘起を避け、均一な配向状態を固定するために、少なくとも２つの６員環を有する液晶性骨格を部分構造として有する環状アルコール又はフェノール又は芳香族ヒドロキシ化合物のアクリル酸又はメタクリル酸エステルである第１の単官能アクリレート又は第１の単官能メタクリレートを含有し、液晶相を示すことを特徴とする重合性液晶組成物を用いることが好ましい。このような単官能アクリレート又は単官能メタクリレートとしては、例えば、一般式（Ｉ）
【００１３】
【化５】
（式中、Ｘは水素原子又はメチル基を表わし、６員環Ａ、Ｂ及びＣはそれぞれ独立的に、
【００１５】
【化６】
を表わし、ｎは０又は１の整数を表わし、ｍは１から４の整数を表わし、Ｙ１及びＹ２はそれぞれ独立的に、単結合、−ＣＨ２ＣＨ２−、−ＣＨ２Ｏ−、−ＯＣＨ２−、−ＣＯＯ−、−ＯＣＯ−、−Ｃ≡Ｃ−、−ＣＨ＝ＣＨ−、−ＣＦ＝ＣＦ−、−（ＣＨ２）４−、−ＣＨ２ＣＨ２ＣＨ２Ｏ−、−ＯＣＨ２ＣＨ２ＣＨ２−、−ＣＨ２＝ＣＨＣＨ２ＣＨ２−又は−ＣＨ２ＣＨ２ＣＨ＝ＣＨ−を表わし、Ｙ３は水素原子、ハロゲン原子、シアノ基、炭素原子数１〜２０のアルキル基、アルコキシ基、アルケニル基又はアルケニルオキシ基を表わす。）で表わされる化合物を挙げることができる。その中でも特に、上記一般式（Ｉ）において、６員環Ａ、Ｂ及びＣはそれぞれ独立的に、
【００１７】
【化７】
を表わし、ｍは１又は２の整数を表わし、Ｙ１及びＹ２はそれぞれ独立的に、単結合又は−Ｃ≡Ｃ−を表わし、Ｙ３はハロゲン原子、シアノ基、炭素原子数１〜２０のアルキル基又はアルコキシ基を表わす化合物が好ましい。
【００１９】
このような化合物の代表的なものの例と、その相転移温度を示すが、本発明で使用することができる単官能アクリレート又は単官能メタクリレート化合物は、これらの化合物に限定されるものではない。
【００２０】
【化８】
【化９】
（上記中、シクロヘキサン環はトランスシクロヘキサン環を表わし、また相転移温度スキームのＣは結晶相、Ｎはネマチック相、Ｓはスメクチック相、Ｉは等方性液体相を表わし、数字は相転移温度を表わす。）
また、本発明で使用する重合性液晶組成物には、これまでに知られている液晶性骨格を部分構造として有する第２の単官能アクリレート又は、第２の単官能メタクリレート化合物を添加してもよい。このとき、得られる重合性液晶組成物は、室温においてエナンチオトロピックなネマチック液晶相を示すことが望ましい。ここで用いることができる単官能アクリレート又は単官能メタクリレートとしては、例えば一般式（ＩＩ）
【００２３】
【化１０】
（式中、Ｒは水素原子又はメチル基を表わし、ｐは２〜１２の整数を表わし、Ｙ４は単結合又は−ＣＯＯ−を表わし、Ｙ５はシアノ基、炭素原子数１〜６のアルキル基、アルコキシ基又はフェニル基を表わす。）で表わされる化合物を挙げることができ、具体的には以下の化合物を挙げることができる。
【００２５】
【化１１】
（式中、Ｒ１、Ｒ２及びＲ３はそれぞれ独立的に、水素原子又はメチル基を表わし、ｊ、ｋ及びｌはそれぞれ独立的に、２〜１２の整数を表わし、Ｒ４は炭素原子数１〜６のアルキル基、アルコキシ基又はフェニル基を表わす。）
このように、本発明で使用する重合性液晶組成物は、第１の単官能（メタ）アクリレートのみを含有しても良く、あるいは第２の単官能（メタ）アクリレートのみを含有しても良く、第１及び第２の単官能（メタ）アクリレートを併用しても良い。
【００２７】
重合性液晶組成物として第１及び第２の単官能（メタ）アクリレートを併用する場合は、第２の単官能（メタ）アクリレートの含有量は、第１の単官能（メタ）アクリレートに対して５０重量％以下であることが好ましい。これは第２の単官能（メタ）アクリレートの含有量が増えるに従って、得られる光学異方体の機械的強度及び耐熱性が劣る傾向があるからである。
【００２８】
また本発明で用いる重合性液晶組成物の誘電率異方性は正であることが必須である。
また本発明で用いる重合性液晶組成物には重合性官能基を有していない液晶化合物を、重合性液晶組成物中の総量が１０重量％を超えない範囲で添加してもよい。重合性官能基を有していない液晶化合物としてはネマチック液晶化合物、スメクチック液晶化合物、コレステリック液晶化合物等の通常この技術分野で液晶と認識されるものであれば特に制限なく用いることができる。しかしながらその添加量が増えるに従い、得られる光学異方体の機械的強度が低下する傾向にあるので、添加量を適宜調整する必要がある。
【００２９】
また、重合性官能基を有しているが、液晶性を示さない化合物も添加することができる。このような化合物としては、通常この技術分野で高分子形成性モノマーあるいは高分子形成性オリゴマーとして認識されるものであればよいが、アクリレート化合物が特に好ましい。
【００３０】
これらの液晶化合物又は重合性化合物は適宜選択して組み合わせて添加してもよいが、少なくとも得られる重合性液晶組成物の液晶性が失われないように、各成分の添加量を調整することが必要である。
【００３１】
また、本発明で使用する重合性液晶組成物には、その重合反応性を向上させることを目的として、光重合開始剤や増感剤を添加してもよい。ここで、使用することができる光重合開始剤としては、例えば、公知のベンゾインエーテル類、ベンゾフェノン類、アセトフェノン類、ベンジルケタール類等を挙げることができる。その添加量は、重合性液晶組成物に対して１０重量％以下が好ましく、５重量％以下が特に好ましい。
【００３２】
更に、本発明で使用する重合性液晶組成物には、その保存安定性を向上させるために、安定剤を添加してもよい。ここで使用することができる安定剤としては公知のヒドロキノン、ヒドロキノンモノアルキルエーテル類、第三ブチルカテコール等を挙げることができる。その安定剤の添加量は０．０５重量％以下が好ましい。
【００３３】
本発明の光学異方体及び光学異方性を有する基板の製造方法は、上述の導電層を有する第１の透明性基板と、導電性を有する第２の基板を電圧印加可能なように配置し、この２枚の基板間に前述の重合性液晶組成物を介在させる。このとき、２枚の基板間の距離は、製造する光学異方体の用途によって適宜調整されるが、０．１〜１００ミクロンの範囲が好ましく、特に０．５〜５０ミクロンの範囲が好ましい。
【００３４】
次いで、２枚の基板間に電圧を印加しながら、第１の透明性基板の側から光を照射する。基板間に電圧を印加する手段としては、通常の液晶表示素子に使用される駆動手段が使用でき、好ましい印加電圧は重合性液晶組成物の誘電率異方性や基板間の距離によって適宜調整されるが、０．５Ｖ以上の交流電圧が好ましい。
【００３５】
光重合は紫外線又は電子線等のエネルギー線を、前述の２枚の基板間に担持された重合性液晶組成物に照射することによって行うのが好ましく、従って少なくとも照射面側の基板は、適当な透明性が与えられていなければならない。重合の際の温度は、重合性液晶組成物の液晶状態が保持される温度でなければならないが、意図しない熱重合の誘起を避ける意味から、できるだけ室温に近い温度で重合させることが好ましい。
【００３６】
次いで、第１の発明においては、光学異方体を製造するために、第１の透明性基板及び第２の基板を剥離することにより、容易に得ることができる。第２の発明においては、光学異方性を有する基板を製造するために、第２の基板を剥離することにより、容易に得ることができる。第３の発明においては、第１及び第２の基板を共に剥離せずに、光学異方性を有する基板を容易に得ることができる。
【００３７】
このとき、基板を容易に剥離するためには、基板に良好な剥離性を付与するために、基板表面に有機材料の薄膜等を形成することが好ましい。このような有機材料として、ポリテトラフルオロエチレン等のフッ素化ポリマーやポリビニルアルコールと１，８−オクタンジオール等のジオール化合物との混合物、及びレシチン等を挙げることができる。また基板と接していない光学異方体の表面を保護する目的で、熱硬化性もしくは光硬化性の樹脂を用いて表面に保護層を形成してもよい。
【００３８】
このような製造方法により製造される光学異方体及び光学異方性を有する基板は、重合性液晶組成物の垂直配向を基板の垂直配向処理によらず得ることができ、内部に垂直配向構造を有し、厚み方向の屈折率が面内の屈折率より大きい、フィルム状の光学異方体及び光学異方性を有する基板を効率よく製造することができる。
【００３９】
【実施例】
以下、本発明の実施例を示し、本発明を更に具体的に説明する。しかしながら、本発明はこれらの実施例に限定されるものではない。
（実施例１）
式（ａ）
【００４０】
【化１２】
の化合物４７．５重量部及び式（ｄ）
【００４２】
【化１３】
の化合物４７．５重量部及び式（ｇ）
【００４４】
【化１４】
の化合物５重量部からなる重合性液晶組成物（Ａ）を調整した。得られた組成物は室温（２５℃）でエナンチオトロピックなネマチック相をしめし、ネマチック相から等方性液体相への転移温度は５２℃であった。また２５℃におけるｎｅ（異常光屈折率）は１．６７、ｎｏ（常光屈折率）は１．５１、誘電率異方性は＋０．７であった。この重合性液晶組成物（Ａ）９９重量部及び光重合開始剤「ＩＲＧ−６５１」（チバガイギー社製）１重量部からなる重合性液晶組成物（Ｂ）を得た。次に２枚のＩＴＯ透明電極付きガラス基板を、１０ミクロンの間隔をもってＩＴＯ面が内側になるように対向させて、この基板間に重合性液晶組成物（Ｂ）を挟持させた。この２枚のＩＴＯ透明電極付きガラス基板間に挟持された重合性液晶組成物を偏光顕微鏡で観察したところ、配向状態は均一ではなく、ランダム配向状態であった。このランダム配向状態の重合性液晶組成物を挟持している２枚のＩＴＯ電極間に電圧が５０Ｖｒｍｓの周波数１ｋＨｚの正弦波を印加したところ、重合性液晶組成物は垂直配向するのがコノスコープ像の観察により確認できた。電圧印加により重合性液晶組成物が垂直配向した状態のまま、室温において紫外線ランプ（ＵＶＰ社製、ＵＶＧＬ−２５）を用いて１６０ｍＪ／ｃｍ２の光量の紫外線を照射して、重合性液晶組成物を光重合し硬化させた。このようにして得られた２枚のＩＴＯ透明電極付きガラス基板間に挟持された光学異方体をコノスコープ観察したところ、重合前の垂直配向がそのまま固定化されていた。またこの光学異方体を２枚の直交する偏光板の間に置いて観察したところ、均一に暗視野になっており、均一な垂直配向が得られていることを確認した。以上のことから、厚み方向の屈折率が面内の屈折率より大きく且つ均一性に優れた光学異方体が得られたことは明らかである。またこの光学異方体を１２０℃の温度に保っても、均一な垂直配向は維持されており、耐熱性も何等問題なかった。
（実施例２）
剥離剤として卵黄レシチンの０．１重量％エタノール溶液を塗布した後に乾燥させたＩＴＯ透明電極付きガラス基板と何も塗布していないＩＴＯ透明電極付きガラス基板を、１０ミクロンの間隔をもってＩＴＯ面を内側になるように対向させてこの間に実施例１で調製した重合性液晶組成物（Ｂ）を挟持させた。この２枚のＩＴＯ透明電極付きガラス基板間に挟持された重合性液晶組成物を偏光顕微鏡で観察したところ、配向状態は均一ではなく、ランダム配向状態であった。このランダム配向状態の重合性液晶組成物を挟持しているＩＴＯ電極間に電圧が５０Ｖｒｍｓの周波数１ｋＨｚの正弦波を印加したところ、重合性液晶組成物は垂直配向するのがコノスコープ像の観察により確認できた。このように電圧印加により重合性液晶組成物が垂直配向した状態で、室温において紫外線ランプ（ＵＶＰ社製、ＵＶＧＬ−２５）を用いて１６０ｍＪ／ｃｍ２の光量の紫外線を照射して、重合性液晶組成物を光重合し硬化させた。次に卵黄レシチンを塗布した基板を剥離して、ＩＴＯ透明電極付きガラス基板上に担持された、光学異方性を有する基板を得た。このようにして得られた光学異方性を有する基板をコノスコープ観察したところ、重合前の垂直配向がそのまま固定化されていた。またこの光学異方性を有する基板を２枚の直交する偏光板の間に置いて観察したところ、均一に暗視野になっており、均一な垂直配向が得られていることを確認した。以上のことから、厚み方向の屈折率が面内の屈折率より大きく且つ均一性に優れた光学異方性を有する基板が得られたことは明らかである。またこの光学異方性を有する基板を１２０℃の温度に保っても、均一な垂直配向は維持されており、耐熱性も何等問題なかった。
（実施例３）
実施例２において、ＩＴＯ透明電極付きガラス基板に代えて、厚さ１ｍｍのアルミニウム板を用いた以外は実施例２と同様にして、重合性液晶組成物を光重合し硬化させた。次にアルミニウム板を剥離して、ＩＴＯ透明電極付きガラス基板上に担持された、光学異方性を有する基板を得た。このようにして得られた光学異方性を有する基板をコノスコープ観察したところ、重合前の垂直配向がそのまま固定化されていた。またこの光学異方性を有する基板を２枚の直交する偏光板の間に置いて観察したところ、均一に暗視野になっており、均一な垂直配向が得られていることを確認した。以上のことから、厚み方向の屈折率が面内の屈折率より大きく且つ均一性に優れた光学異方性を有する基板が得られたことは明らかである。またこの光学異方体を１２０℃の温度に保っても、均一な垂直配向は維持されており、耐熱性も何等問題なかった。
（実施例４）
剥離剤として卵黄レシチンの０．１重量％エタノール溶液を塗布した後に乾燥させたＩＴＯ透明電極付きガラス基板と何も塗布していないＩＴＯ透明電極付きガラス基板を、２０ミクロンの間隔をもってＩＴＯ面を内側になるように対向させてこの間に実施例１で調製した重合性液晶組成物（Ｂ）を挟持させた。この２枚のＩＴＯ透明電極付きガラス基板間に挟持された重合性液晶組成物を偏光顕微鏡で観察したところ、配向状態は均一ではなく、ランダム配向状態であった。このランダム配向状態の重合性液晶組成物を挟持しているＩＴＯ電極間に電圧が１００Ｖｒｍｓの周波数１ｋＨｚの正弦波を印加したところ、重合性液晶組成物は垂直配向するのがコノスコープ像の観察により確認できた。このように電圧印加により重合性液晶組成物が垂直配向した状態で、室温において紫外線ランプ（ＵＶＰ社製、ＵＶＧＬ−２５）を用いて１６０ｍＪ／ｃｍ２の光量の紫外線を照射して、重合性液晶組成物を光重合し硬化させた。次に卵黄レシチンを塗布した基板を剥離して、ＩＴＯ透明電極付きガラス基板上に担持された、光学異方性を有する基板を得た。更にこの光学異方性を有する基板を蒸留水に３０分間浸した後に、更にＩＴＯ透明電極付きガラス基板を光学異方体から剥離して、独立したフィルム状の光学異方体を得た。このようにして得られた光学異方体をコノスコープ観察したところ、重合前の垂直配向がそのまま固定化されていた。またこの光学異方体を２枚の直交する偏光板の間に置いて観察したところ、均一に暗視野になっており、均一な垂直配向が得られていることを確認した。以上のことから、厚み方向の屈折率が面内の屈折率より大きく且つ均一性に優れた光学異方体が得られたのは明かである。またこの光学異方体を１２０℃の温度に保っても、均一な垂直配向は維持されており、耐熱性も何等問題なかった。
【００４６】
【発明の効果】
本発明の光学異方体及び光学異方性を有する基板の製造方法は、光照射時に電圧を印加することにより、従来のような煩わしい基板の配向処理を施す場合に比べて、重合性液晶組成物を容易に垂直配向させることができる。従って、本発明の製造方法は、厚み方向の屈折率が面内の屈折率より大きなフィルム状の光学異方体及び光学異方性を有する基板の製造方法として、極めて有用である。[0001]
[Industrial applications]
The present invention relates to an optically anisotropic material useful for eliminating or reducing the viewing angle dependence of a liquid crystal display element, and a method for manufacturing a substrate having optical anisotropy using the optically anisotropic material.
[0002]
[Prior art]
In order to reduce the viewing angle dependency of a liquid crystal display element, a means using a film (optically anisotropic body) having a refractive index in a thickness direction larger than an in-plane refractive index as a compensator is known (M. Akatsuka et al. Japan Display '89, 336, 1989). As such an optically anisotropic body, one using a liquid crystalline polymer is disclosed in JP-A-5-27235 and JP-A-5-34678. However, these optically anisotropic materials fix the vertical alignment structure of the liquid crystalline polymer in a glassy state, and if the temperature exceeds the glass transition point of the liquid crystalline polymer, the alignment structure is destroyed. There was the disadvantage that it was limited by the glass transition point. In addition, the viscosity of high-molecular liquid crystals is higher than that of low-molecular liquid crystals, and it takes time to obtain a vertical alignment state, which has the disadvantage of reducing productivity. This drawback has become more apparent as the shape of the liquid crystal polymer is designed to be higher, as the shape of the liquid crystal polymer is increased.
[0003]
In order to solve these problems, the present inventors have prepared a polymerizable liquid crystal composition having liquid crystallinity at room temperature, by supporting the polymerizable liquid crystal composition between substrates subjected to a vertical alignment treatment, and then vertically polymerizing the composition. A substrate having optical anisotropy has been proposed earlier.
[0004]
However, although the time required to obtain a uniform vertical alignment state has been reduced by this technique, there has been the inconvenience that the vertical alignment processing must be performed on the substrate surface.
[0005]
[Problems to be solved by the invention]
The problem to be solved by the present invention is to provide a production method which can be more easily obtained as a means for vertically aligning a polymerizable liquid crystal composition with respect to a substrate surface, without using a conventional vertical alignment treatment. Accordingly, the object is to further improve the production efficiency of an optically anisotropic body having a vertical alignment structure inside.
[0006]
[Means for Solving the Problems]
The present inventors diligently studied means for solving the above problems, and as a result, found that such problems can be solved by applying a voltage to the vertical alignment of the polymerizable liquid crystal composition liquid crystal, and came to provide the present invention. .
[0007]
That is, the present invention provides, as a first invention, (1) a first step of interposing a polymerizable liquid crystal composition between a first transparent substrate having a conductive layer and a second substrate having conductivity;
(2) a second step of irradiating light from the side of the first transparent substrate while applying a voltage between the two substrates, and (3) peeling off the first transparent substrate and the second substrate. And a method for producing an optically anisotropic body having a third step.
[0008]
Further, the present invention provides, as a second invention, (1) a first step of interposing a polymerizable liquid crystal composition between a first transparent substrate having a conductive layer and a second substrate having conductivity;
(2) an optical system including a second step of irradiating light from the side of the first transparent substrate while applying a voltage between the two substrates, and (3) a third step of separating the second substrate. Provided is a method for manufacturing a substrate having anisotropy.
[0009]
Furthermore, the present invention provides, as a third invention, (1) a first step of interposing a polymerizable liquid crystal composition between two transparent substrates having a conductive layer, and (2) a step between the two substrates. Provided is a method for manufacturing a substrate having optical anisotropy, comprising a second step of irradiating light from the side of a first transparent substrate while applying a voltage.
[0010]
Hereinafter, the first invention, the second invention, and the third invention will be described in more detail.
As the first transparent substrate used in the present invention, for example, a glass or plastic substrate having a conductive layer is preferable, and specific examples include a glass substrate with ITO and a plastic substrate with ITO. These substrates can be easily obtained by using means such as vapor deposition, plating, and printing on a non-conductive glass or plastic substrate, but commercially available substrates with ITO can also be used.
[0011]
The second substrate used in the present invention may be a transparent substrate or an opaque substrate as long as the substrate itself has conductivity, and may be an organic material or an inorganic material. It can be used regardless. Specifically, examples of the inorganic material include metals such as copper, gold, silver, tin, lead, iron, nickel, aluminum, and ITO (indium tin oxide), and metal oxides. Examples thereof include conductive rubber and conductive plastic.
[0012]
The polymerizable liquid crystal composition used in the present invention includes a liquid crystal having at least two 6-membered rings in order to avoid unintended thermal polymerization during photopolymerization in a liquid crystal state and to fix a uniform alignment state. A first monofunctional acrylate or a first monofunctional methacrylate, which is an acrylic acid or methacrylic acid ester of a cyclic alcohol or phenol or an aromatic hydroxy compound having a functional skeleton as a partial structure, and exhibits a liquid crystal phase. It is preferable to use a polymerizable liquid crystal composition. Examples of such a monofunctional acrylate or monofunctional methacrylate include, for example, those represented by the general formula (I)
[0013]
Embedded image
(Wherein X represents a hydrogen atom or a methyl group, and the 6-membered rings A, B and C each independently represent
[0015]
Embedded image
And n represents an integer of 0 or 1, m represents an integer of 1 to 4, Y 1 and Y 2 each independently represent a single bond, —CH 2 CH 2 —, —CH 2 O—, -OCH 2 -, - COO -, - OCO -, - C≡C -, - CH = CH -, - CF = CF -, - (CH 2) 4 -, - CH 2 CH 2 CH 2 O -, - OCH 2 CH 2 CH 2 —, —CH 2 ＣＨCHCH 2 CH 2 — or —CH 2 CH 2 CH ＝ CH—, wherein Y 3 is a hydrogen atom, a halogen atom, a cyano group, or an alkyl having 1 to 20 carbon atoms. Represents a group, an alkoxy group, an alkenyl group or an alkenyloxy group. )). Among them, particularly, in the above general formula (I), the 6-membered rings A, B and C are each independently
[0017]
Embedded image
And m represents an integer of 1 or 2, Y 1 and Y 2 each independently represent a single bond or —C≡C—, and Y 3 represents a halogen atom, a cyano group, or a carbon atom having 1 to 20 carbon atoms. The compound which represents an alkyl group or an alkoxy group is preferred.
[0019]
Representative examples of such compounds and their phase transition temperatures are shown, but the monofunctional acrylate or methacrylate compounds that can be used in the present invention are not limited to these compounds.
[0020]
Embedded image
Embedded image
(In the above, the cyclohexane ring represents a transcyclohexane ring, and in the phase transition temperature scheme, C represents a crystal phase, N represents a nematic phase, S represents a smectic phase, and I represents an isotropic liquid phase, and a number represents a phase transition temperature. Show.)
Further, to the polymerizable liquid crystal composition used in the present invention, a second monofunctional acrylate or a second monofunctional methacrylate compound having a liquid crystal skeleton known as a partial structure as a partial structure may be added. Good. At this time, the resulting polymerizable liquid crystal composition desirably exhibits an enantiomeric nematic liquid crystal phase at room temperature. Examples of the monofunctional acrylate or monofunctional methacrylate that can be used here include, for example, those represented by the general formula (II)
[0023]
Embedded image
(Wherein, R represents a hydrogen atom or a methyl group, p represents an integer of 2 to 12, Y 4 represents a single bond or —COO—, Y 5 represents a cyano group, or an alkyl having 1 to 6 carbon atoms. Group, an alkoxy group or a phenyl group). Specific examples thereof include the following compounds.
[0025]
Embedded image
(Wherein, R 1 , R 2 and R 3 each independently represent a hydrogen atom or a methyl group, j, k and l each independently represent an integer of 2 to 12, and R 4 represents a carbon atom Represents an alkyl group, an alkoxy group or a phenyl group represented by Formulas 1 to 6.)
Thus, the polymerizable liquid crystal composition used in the present invention may contain only the first monofunctional (meth) acrylate, or may contain only the second monofunctional (meth) acrylate. , First and second monofunctional (meth) acrylates may be used in combination.
[0027]
When the first and second monofunctional (meth) acrylates are used together as the polymerizable liquid crystal composition, the content of the second monofunctional (meth) acrylate is based on the first monofunctional (meth) acrylate. It is preferably at most 50% by weight. This is because as the content of the second monofunctional (meth) acrylate increases, the mechanical strength and heat resistance of the obtained optically anisotropic material tend to be inferior.
[0028]
Further, it is essential that the polymerizable liquid crystal composition used in the present invention has a positive dielectric anisotropy.
Further, a liquid crystal compound having no polymerizable functional group may be added to the polymerizable liquid crystal composition used in the present invention in a range where the total amount in the polymerizable liquid crystal composition does not exceed 10% by weight. As the liquid crystal compound having no polymerizable functional group, a nematic liquid crystal compound, a smectic liquid crystal compound, a cholesteric liquid crystal compound and the like can be used without particular limitation as long as they are generally recognized as liquid crystals in this technical field. However, as the addition amount increases, the mechanical strength of the obtained optically anisotropic body tends to decrease. Therefore, it is necessary to appropriately adjust the addition amount.
[0029]
In addition, a compound having a polymerizable functional group but not exhibiting liquid crystallinity can be added. As such a compound, any compound which is generally recognized as a polymer-forming monomer or a polymer-forming oligomer in this technical field may be used, and an acrylate compound is particularly preferable.
[0030]
These liquid crystal compounds or polymerizable compounds may be appropriately selected and added in combination.However, at least the amount of each component added may be adjusted so that the liquid crystallinity of the obtained polymerizable liquid crystal composition is not lost. is necessary.
[0031]
Further, a photopolymerization initiator or a sensitizer may be added to the polymerizable liquid crystal composition used in the present invention for the purpose of improving the polymerization reactivity. Here, examples of the photopolymerization initiator that can be used include known benzoin ethers, benzophenones, acetophenones, and benzyl ketals. The addition amount is preferably 10% by weight or less, particularly preferably 5% by weight or less, based on the polymerizable liquid crystal composition.
[0032]
Further, a stabilizer may be added to the polymerizable liquid crystal composition used in the present invention in order to improve the storage stability. Examples of the stabilizer that can be used here include known hydroquinone, hydroquinone monoalkyl ethers, and tert-butylcatechol. The amount of the stabilizer is preferably 0.05% by weight or less.
[0033]
In the method for manufacturing a substrate having an optical anisotropic body and an optical anisotropy according to the present invention, a first transparent substrate having the above-described conductive layer and a second substrate having conductivity are arranged so that a voltage can be applied. Then, the aforementioned polymerizable liquid crystal composition is interposed between the two substrates. At this time, the distance between the two substrates is appropriately adjusted depending on the use of the optically anisotropic body to be manufactured, but is preferably in the range of 0.1 to 100 microns, and particularly preferably in the range of 0.5 to 50 microns.
[0034]
Next, light is irradiated from the side of the first transparent substrate while a voltage is applied between the two substrates. As a means for applying a voltage between the substrates, a driving means used for a normal liquid crystal display element can be used, and a preferable applied voltage is appropriately adjusted depending on the dielectric anisotropy of the polymerizable liquid crystal composition and the distance between the substrates. However, an AC voltage of 0.5 V or more is preferable.
[0035]
The photopolymerization is preferably performed by irradiating an energy ray such as an ultraviolet ray or an electron beam to the polymerizable liquid crystal composition supported between the two substrates described above. Transparency must be provided. The temperature at the time of the polymerization must be a temperature at which the liquid crystal state of the polymerizable liquid crystal composition is maintained, but it is preferable to perform the polymerization at a temperature as close to room temperature as possible from the viewpoint of avoiding unintended thermal polymerization.
[0036]
Next, in the first invention, in order to manufacture an optically anisotropic body, the optically anisotropic body can be easily obtained by peeling the first transparent substrate and the second substrate. In the second invention, in order to manufacture a substrate having optical anisotropy, it can be easily obtained by peeling the second substrate. In the third invention, a substrate having optical anisotropy can be easily obtained without peeling off the first and second substrates together.
[0037]
At this time, in order to easily peel the substrate, it is preferable to form a thin film of an organic material or the like on the surface of the substrate in order to impart good peelability to the substrate. Examples of such an organic material include a fluorinated polymer such as polytetrafluoroethylene, a mixture of polyvinyl alcohol and a diol compound such as 1,8-octanediol, and lecithin. In order to protect the surface of the optically anisotropic body not in contact with the substrate, a protective layer may be formed on the surface using a thermosetting or photocurable resin.
[0038]
The substrate having an optical anisotropic material and optical anisotropy manufactured by such a manufacturing method can obtain the vertical alignment of the polymerizable liquid crystal composition without depending on the vertical alignment processing of the substrate, and has a vertical alignment structure inside. And a film-like optically anisotropic body and a substrate having optical anisotropy, in which the refractive index in the thickness direction is larger than the in-plane refractive index, can be efficiently produced.
[0039]
【Example】
Hereinafter, examples of the present invention will be shown, and the present invention will be described more specifically. However, the invention is not limited to these examples.
(Example 1)
Equation (a)
[0040]
Embedded image
47.5 parts by weight of the compound of formula (d)
[0042]
Embedded image
47.5 parts by weight of a compound of the formula (g)
[0044]
Embedded image
A polymerizable liquid crystal composition (A) consisting of 5 parts by weight of the compound (A) was prepared. The obtained composition showed an enantiomeric nematic phase at room temperature (25 ° C.), and the transition temperature from the nematic phase to the isotropic liquid phase was 52 ° C. The n e (extraordinary refractive index) at 25 ° C. is 1.67, n o (ordinary refractive index) is 1.51, the dielectric anisotropy was +0.7. A polymerizable liquid crystal composition (B) comprising 99 parts by weight of the polymerizable liquid crystal composition (A) and 1 part by weight of a photopolymerization initiator "IRG-651" (manufactured by Ciba Geigy) was obtained. Next, two glass substrates with ITO transparent electrodes were opposed to each other with an interval of 10 μm such that the ITO surface was on the inside, and the polymerizable liquid crystal composition (B) was sandwiched between the substrates. When the polymerizable liquid crystal composition sandwiched between the two glass substrates with ITO transparent electrodes was observed with a polarizing microscope, the alignment state was not uniform but a random alignment state. When a sine wave having a voltage of 50 Vrms and a frequency of 1 kHz was applied between two ITO electrodes sandwiching the polymerizable liquid crystal composition in a random alignment state, the polymerizable liquid crystal composition was vertically aligned. Was confirmed by observation. The polymerizable liquid crystal composition was irradiated with 160 mJ / cm 2 of ultraviolet light using an ultraviolet lamp (manufactured by UVP, UVGL-25) at room temperature while the polymerizable liquid crystal composition was vertically aligned by voltage application. Was photopolymerized and cured. When an optically anisotropic material sandwiched between the two glass substrates with ITO transparent electrodes obtained in this way was observed with a conoscope, the vertical alignment before polymerization was fixed as it was. Further, when this optically anisotropic body was placed between two orthogonal polarizing plates and observed, it was confirmed that a dark field was uniformly obtained and uniform vertical alignment was obtained. From the above, it is apparent that an optically anisotropic body having a higher refractive index in the thickness direction than the in-plane refractive index and excellent in uniformity was obtained. Even when the optically anisotropic body was kept at a temperature of 120 ° C., uniform vertical alignment was maintained, and there was no problem with heat resistance.
(Example 2)
A 0.1% by weight ethanol solution of egg yolk lecithin was applied as a peeling agent and then dried. The glass substrate with ITO transparent electrode and the glass substrate with no ITO transparent electrode were coated with the ITO surface inside at intervals of 10 microns. And the polymerizable liquid crystal composition (B) prepared in Example 1 was interposed between them. When the polymerizable liquid crystal composition sandwiched between the two glass substrates with ITO transparent electrodes was observed with a polarizing microscope, the alignment state was not uniform but a random alignment state. When a sine wave having a frequency of 1 kHz and a voltage of 50 Vrms was applied between the ITO electrodes sandwiching the polymerizable liquid crystal composition in the random alignment state, the polymerizable liquid crystal composition was vertically aligned by observing a conoscopic image. It could be confirmed. In the state where the polymerizable liquid crystal composition is vertically aligned by the application of the voltage as described above, the polymerizable liquid crystal is irradiated with ultraviolet light of 160 mJ / cm 2 at room temperature using an ultraviolet lamp (manufactured by UVP, UVGL-25). The composition was photopolymerized and cured. Next, the substrate coated with egg yolk lecithin was peeled off to obtain a substrate having optical anisotropy supported on a glass substrate with an ITO transparent electrode. When the thus obtained substrate having optical anisotropy was observed with a conoscope, the vertical alignment before polymerization was fixed as it was. Further, when the substrate having the optical anisotropy was placed between two orthogonal polarizing plates and observed, it was confirmed that the dark field was uniform and a uniform vertical alignment was obtained. From the above, it is apparent that a substrate having a refractive index in the thickness direction larger than the in-plane refractive index and having optical anisotropy excellent in uniformity was obtained. Even when the substrate having this optical anisotropy was maintained at a temperature of 120 ° C., uniform vertical alignment was maintained, and there was no problem with heat resistance.
(Example 3)
A polymerizable liquid crystal composition was photopolymerized and cured in the same manner as in Example 2 except that an aluminum plate having a thickness of 1 mm was used instead of the glass substrate provided with the ITO transparent electrode. Next, the aluminum plate was peeled off to obtain a substrate having optical anisotropy supported on a glass substrate with an ITO transparent electrode. When the thus obtained substrate having optical anisotropy was observed with a conoscope, the vertical alignment before polymerization was fixed as it was. Further, when the substrate having the optical anisotropy was placed between two orthogonal polarizing plates and observed, it was confirmed that the dark field was uniform and a uniform vertical alignment was obtained. From the above, it is apparent that a substrate having a refractive index in the thickness direction larger than the in-plane refractive index and having optical anisotropy excellent in uniformity was obtained. Even when the optically anisotropic body was kept at a temperature of 120 ° C., uniform vertical alignment was maintained, and there was no problem with heat resistance.
(Example 4)
A 0.1% by weight ethanol solution of egg yolk lecithin was applied as a peeling agent and then dried. The glass substrate with ITO transparent electrode and the glass substrate with no ITO transparent electrode were coated with the ITO surface inside at a spacing of 20 microns. And the polymerizable liquid crystal composition (B) prepared in Example 1 was interposed between them. When the polymerizable liquid crystal composition sandwiched between the two glass substrates with ITO transparent electrodes was observed with a polarizing microscope, the alignment state was not uniform but a random alignment state. When a sine wave having a voltage of 100 Vrms and a frequency of 1 kHz was applied between the ITO electrodes sandwiching the polymerizable liquid crystal composition in the random alignment state, the polymerizable liquid crystal composition was vertically aligned. It could be confirmed. In the state where the polymerizable liquid crystal composition is vertically aligned by the application of the voltage as described above, the polymerizable liquid crystal is irradiated with ultraviolet light of 160 mJ / cm 2 at room temperature using an ultraviolet lamp (manufactured by UVP, UVGL-25). The composition was photopolymerized and cured. Next, the substrate coated with egg yolk lecithin was peeled off to obtain a substrate having optical anisotropy supported on a glass substrate with an ITO transparent electrode. After the substrate having the optical anisotropy was immersed in distilled water for 30 minutes, the glass substrate with the ITO transparent electrode was further peeled off from the optically anisotropic body to obtain an independent film-shaped optically anisotropic body. When the optically anisotropic body thus obtained was observed with a conoscope, the vertical alignment before polymerization was fixed as it was. Further, when this optically anisotropic body was placed between two orthogonal polarizing plates and observed, it was confirmed that a dark field was uniformly obtained and uniform vertical alignment was obtained. From the above, it is apparent that an optically anisotropic body having a larger refractive index in the thickness direction than the in-plane refractive index and having excellent uniformity was obtained. Even when the optically anisotropic body was kept at a temperature of 120 ° C., uniform vertical alignment was maintained, and there was no problem with heat resistance.
[0046]
【The invention's effect】
The method for producing a substrate having an optical anisotropic body and an optical anisotropy of the present invention, by applying a voltage at the time of light irradiation, compared with a conventional case of performing a cumbersome substrate alignment treatment, the polymerizable liquid crystal composition The object can be easily vertically aligned. Therefore, the production method of the present invention is extremely useful as a method for producing a film-shaped optically anisotropic body and a substrate having optical anisotropy in which the refractive index in the thickness direction is larger than the in-plane refractive index.
Claims (10)
（２）前記２枚の基板間に室温で電圧を印加しながら、第１の透明性基板の側から光を照射する第２工程、及び
（３）第１の透明性基板及び第２の基板を剥離する第３工程
を有する光学異方体の製造方法。(1) Acrylic acid of cyclic alcohol or phenol having a liquid crystal skeleton having at least two 6-membered rings as a partial structure between a first transparent substrate having a conductive layer and a second substrate having conductivity. A first step of containing a first monofunctional acrylate or a first monofunctional methacrylate that is a methacrylate, and interposing a polymerizable liquid crystal composition exhibiting a liquid crystal phase at room temperature.
(2) a second step of irradiating light from the side of the first transparent substrate while applying a voltage between the two substrates at room temperature , and (3) a first transparent substrate and a second substrate A method for producing an optically anisotropic body having a third step of peeling off.
（２）前記２枚の基板間に室温で電圧を印加しながら、第１の透明性基板の側から光を照射する第２工程、及び
（３）第２の基板を剥離する第３工程
を有する光学異方性を有する基板の製造方法。(1) Acrylic acid of cyclic alcohol or phenol having a liquid crystal skeleton having at least two 6-membered rings as a partial structure between a first transparent substrate having a conductive layer and a second substrate having conductivity. A first step of containing a first monofunctional acrylate or a first monofunctional methacrylate that is a methacrylate, and interposing a polymerizable liquid crystal composition exhibiting a liquid crystal phase at room temperature.
(2) a second step of irradiating light from the first transparent substrate side while applying a voltage between the two substrates at room temperature , and (3) a third step of peeling the second substrate. A method for producing a substrate having optical anisotropy.
（２）前記２枚の基板間に室温で電圧を印加しながら、第１の透明性基板の側から光を照射する第２工程
を有する光学異方性を有する基板の製造方法。(1) A first unit which is an acrylic or methacrylic acid ester of a cyclic alcohol or phenol having a liquid crystal skeleton having at least two 6-membered rings as a partial structure between two transparent substrates having a conductive layer. A first step of interposing a polymerizable liquid crystal composition containing a functional acrylate or a first monofunctional methacrylate and exhibiting a liquid crystal phase at room temperature, and (2) applying a voltage between the two substrates at room temperature , A method for producing a substrate having optical anisotropy, comprising a second step of irradiating light from the side of the first transparent substrate.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15457494A JP3579921B2 (en) | 1994-07-06 | 1994-07-06 | Manufacturing method of optical anisotropic body |
| DE69419120T DE69419120T2 (en) | 1993-12-24 | 1994-12-23 | Polymerizable liquid crystal composition and optically anisotropic film containing such a composition |
| EP94120614A EP0659865B1 (en) | 1993-12-24 | 1994-12-23 | Polymerizable liquid crystal composition and optically anisotropic film comprising the same |
| US08/657,526 US5863457A (en) | 1993-12-24 | 1996-06-04 | Polymerizable liquid crystal composition and optically anisotropic film comprising the same |
| HK98109469A HK1008679A1 (en) | 1993-12-24 | 1998-07-28 | Polymerizable liquid crystal composition and optically anisotropic film comprising the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15457494A JP3579921B2 (en) | 1994-07-06 | 1994-07-06 | Manufacturing method of optical anisotropic body |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0821915A JPH0821915A (en) | 1996-01-23 |
| JP3579921B2 true JP3579921B2 (en) | 2004-10-20 |
Family
ID=15587208
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15457494A Expired - Lifetime JP3579921B2 (en) | 1993-12-24 | 1994-07-06 | Manufacturing method of optical anisotropic body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3579921B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5773178A (en) * | 1996-09-13 | 1998-06-30 | Japan Synthetic Rubber Co, Ltd. | Process for producing a patterned anisotropic polymeric film |
| US7244798B2 (en) | 2002-10-01 | 2007-07-17 | Nippon Oil Corporation | (Meth) acrylic compound having an oxetanyl group and liquid crystal film produced by using same |
| JP4453814B2 (en) * | 2003-11-12 | 2010-04-21 | Ｊｓｒ株式会社 | Polymerizable compound and mixture, and method for producing liquid crystal display device |
| JP4440817B2 (en) | 2005-03-31 | 2010-03-24 | 富士フイルム株式会社 | An optically anisotropic film, a brightness enhancement film, a laminated optical film, and an image display device using them. |
-
1994
- 1994-07-06 JP JP15457494A patent/JP3579921B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0821915A (en) | 1996-01-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0659865B1 (en) | Polymerizable liquid crystal composition and optically anisotropic film comprising the same | |
| TWI778255B (en) | Liquid crystal device including insulating film, light control window and production method | |
| JP4207233B2 (en) | Liquid crystal composition and optical anisotropic body using the same | |
| JPH08231958A (en) | Polymerizable liquid crystal composition and method for producing optically anisotropic substance | |
| JPH083111A (en) | Polymerizable liquid crystal composition and optical anisotropic body using the same | |
| JPH07294735A (en) | Substrate with optical anisotropy | |
| JP5178922B2 (en) | Liquid crystal / polymer composite, liquid crystal display using the same, and method for producing liquid crystal / polymer composite. | |
| JP3579922B2 (en) | Optical anisotropic film and liquid crystal display device using the same | |
| KR20180037206A (en) | Polymerizable liquid crystal composition and optical anisotropic material using the same | |
| JP4802451B2 (en) | Polymerizable liquid crystal composition and polymer thereof | |
| JP4334028B2 (en) | Manufacturing method of liquid crystal display element | |
| WO2008105218A1 (en) | Elliptical polarizing plate for vertically aligned liquid crystal display and vertically aligned liquid crystal display using the same | |
| JP2012042923A (en) | Method for manufacturing liquid crystal display device | |
| JP3734044B2 (en) | Polymerizable liquid crystal composition and method for producing optical anisotropic body | |
| JP3579921B2 (en) | Manufacturing method of optical anisotropic body | |
| CN111198452B (en) | Liquid crystal display device having a plurality of pixel electrodes | |
| JP3617653B2 (en) | Method for producing substrate having optical anisotropy | |
| JP3677817B2 (en) | POLYMER LENS AND METHOD FOR PRODUCING POLYMER LENS | |
| US5378391A (en) | Liquid crystal film | |
| CN110964539B (en) | Liquid crystal composition, high molecular liquid crystal alignment polymer, liquid crystal display element and liquid crystal display | |
| JP2725283B2 (en) | Liquid crystal device and method of manufacturing the same | |
| JPH0953074A (en) | Liquid crystal display device and method of manufacturing liquid crystal display device | |
| CN111198459B (en) | Liquid crystal display device having a plurality of pixel electrodes | |
| JP3651614B2 (en) | Manufacturing method of optical anisotropic body and alignment film forming material used therefor | |
| JP3489129B2 (en) | Liquid crystal device |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20040113 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20040126 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20040629 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20040712 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20080730 Year of fee payment: 4 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20090730 Year of fee payment: 5 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20090730 Year of fee payment: 5 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100730 Year of fee payment: 6 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100730 Year of fee payment: 6 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110730 Year of fee payment: 7 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110730 Year of fee payment: 7 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120730 Year of fee payment: 8 |
|
| S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120730 Year of fee payment: 8 |
|
| R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120730 Year of fee payment: 8 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120730 Year of fee payment: 8 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130730 Year of fee payment: 9 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| EXPY | Cancellation because of completion of term |