TW201224125A - Polymerizable liquid crystal composition - Google Patents

Polymerizable liquid crystal composition Download PDF

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TW201224125A
TW201224125A TW100132720A TW100132720A TW201224125A TW 201224125 A TW201224125 A TW 201224125A TW 100132720 A TW100132720 A TW 100132720A TW 100132720 A TW100132720 A TW 100132720A TW 201224125 A TW201224125 A TW 201224125A
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liquid crystal
film
polymerizable liquid
phase
compound
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TWI550069B (en
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Nobuyuki Hatanaka
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Sumitomo Chemical Co
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/02Liquid crystal materials characterised by optical, electrical or physical properties of the components, in general
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/10Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
    • C09K19/20Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters or ethers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/34Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells

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  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Nonlinear Science (AREA)
  • Optics & Photonics (AREA)
  • General Physics & Mathematics (AREA)
  • Liquid Crystal (AREA)
  • Polarising Elements (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Liquid Crystal Substances (AREA)
  • Polymerisation Methods In General (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The present invention relates to a polymerizable liquid crystal composition containing a polymerizable liquid crystal compound showing smetic phase, a leveling agent and a solvent. Wherein, the leveling agent is selected from at least one of the groups consisting of a leveling agent containing a polyacrylate compound as a main component and a leveling agent containing a fluorine atom-containing compound as a main component. The content of the leveling agent is greater than 0.3 part by mass and less than 5 parts by mass relative to 100 parts by mass of the polymerizable liquid crystal compound.

Description

201224125 六、發明說明: 【發明所屬之技術領域】 本發明係關於一種聚合性液晶組合物。 【先前技術】 液晶顯示裝置中使用有偏光膜、相位差膜等光學膜。 又,曰本專利特表2008_547062號公報中揭示有—種用以 製造此種光學膜之含有聚合性液晶化合物、光聚合起始劑 及溶劑之聚合性液晶組合物。 【發明内容】 本發明提供如下者: [1] 一種聚合性液晶組合物,其係含有顯示層列相之聚 合性液晶化合物、調平劑及溶劑者,並且調平劑係選自由 以聚丙烯酸酯化合物為主成分之調平劑及以含氟原子之化 合物為主成分之調平劑所組成之群中之至少丨種,調平劑 之含里相對於聚合性液晶化合物100質量份為〇3質量份以 上且5質量份以下; [2] 如[1]之聚合性液晶組合物,其,聚合性液晶化合物 係於顯示層列相之溫度與顯示等向相之溫度之間顯示㈣ 相者; [3] 如[1]或[2]之聚合性液晶組合物,其進而含有 色素; [4] 一種光學膜,其係藉由使如Π]至[3]中任一項之聚人 性液晶組合物中所含之聚合性液晶化合物聚合而獲得;。 [5] 種光學膜之製造方法,其包括下述步驟⑴、步驟 158656.doc 201224125 (2)及步驟(3): 步驟(1):將如[1]至[3]中任一項之聚合性液晶組合物塗 佈於基板上而獲得塗佈膜之步驟, 步驟(2):於步驟(1)中獲得之塗佈膜中形成液晶相之步 驟, 步驟(3):藉由使步驟(2)中獲得之形成有液晶相之膜中 所含的聚合性液晶化合物聚合而獲得光學膜之步驟; [6] 如[5]之製造方法,其中液晶相為層列相; [7] 如[5]或[6]之製造方法,其中步驟(2)係藉由將步驟〇) 中獲得之塗佈膜加熱至塗佈膜中所含之聚合性液晶化合物 轉移至向列相之溫度以上,繼而將該聚合性液晶化合物冷 卻至顯示層列相之溫度,而獲得該聚合性液晶化合物配向 為層列相之膜的步驟; [8] —種顯示裝置,其含有如[4]之光學膜; [9] 一種顯示裝置,其含有藉由如[5]之製造方法而獲得 之光學膜; [10] —種顯示裝置,其含有藉由如[6]或[7]之製造方法而 獲得之光學膜。 【實施方式】 於本發明中’所謂「光學膜」,係指可透射光之膜,且 係具有光學性之功能之膜。所謂光學性之功能,係指吸 收、反射、繞射、散射、折射、雙折射等。 作為光學膜之一種的相位差膜係用於將直線偏光轉換成 圓偏光或橢圓偏光,或者相反將圓偏光或橢圓偏光轉換成 158656.doc 201224125 直線偏光。 作為光學膜之一種的偏光膜係用於將未偏光之入射光分 解為正交之2種偏光成分,.使一種偏光成分透射,並將另 一種偏光成分吸收。將透射之偏光成分之軸方向稱為透射 軸’吸收之偏光成分之轴方向稱為吸收軸。 本發明之聚合性液晶組合物含有顯示層列相之聚合性液 晶化合物、調平劑及溶劑,並且調平劑係選自由以聚丙稀 酸醋化合物為主成分之調平劑及以含氟原子之化合物為主 成分之調平劑所組成之群中之至少丨種,調平劑之含量相 對於聚合性液晶化合物100質量份為0 3質量份以上且5質 量份以下。 聚合性液晶化合物係具有聚合性基且顯示液晶性之化合 物。聚合性基係指參與聚合性液晶化合物之聚合反應的 基。 〜 聚合性液晶化合物係顯示層列相之聚合性液晶化合物, 較佳為於顯示層列相之溫度與顯示等向相之溫度之間顯干 向列相之聚合性液晶化合物。若聚合性液晶化合物為此種 化合物,則有可容易地獲得水平配向之層列相之傾向。 作為層列相’可列舉:層列型A相、層㈣相、層列201224125 VI. Description of the Invention: [Technical Field of the Invention] The present invention relates to a polymerizable liquid crystal composition. [Prior Art] An optical film such as a polarizing film or a retardation film is used for the liquid crystal display device. Further, a polymerizable liquid crystal composition containing a polymerizable liquid crystal compound, a photopolymerization initiator, and a solvent for producing such an optical film is disclosed in Japanese Laid-Open Patent Publication No. 2008-547062. SUMMARY OF THE INVENTION The present invention provides the following: [1] A polymerizable liquid crystal composition comprising a polymerizable liquid crystal compound exhibiting a smectic phase, a leveling agent, and a solvent, and the leveling agent is selected from the group consisting of polyacrylic acid. At least one of the group consisting of a leveling agent containing the ester compound as a main component and a leveling agent containing a fluorine atom-containing compound as a main component, and the content of the leveling agent is 100 parts by mass relative to the polymerizable liquid crystal compound. [2] The polymerizable liquid crystal composition according to [1], wherein the polymerizable liquid crystal compound is displayed between the temperature of the display layer phase and the temperature of the display isotropic phase (IV) phase. [3] The polymerizable liquid crystal composition according to [1] or [2], which further contains a pigment; [4] an optical film which is obtained by any one of Π] to [3] The polymerizable liquid crystal compound contained in the human liquid crystal composition is obtained by polymerization; [5] A method for producing an optical film, comprising the following steps (1), 158656.doc 201224125 (2), and step (3): Step (1): the method of any one of [1] to [3] a step of coating a polymerizable liquid crystal composition on a substrate to obtain a coating film, a step (2): a step of forming a liquid crystal phase in the coating film obtained in the step (1), and a step (3): by making the step (2) A step of obtaining a polymer film by polymerizing a polymerizable liquid crystal compound contained in a film having a liquid crystal phase obtained in (2); [6] The method of [5], wherein the liquid crystal phase is a smectic phase; [7] The manufacturing method of [5] or [6], wherein the step (2) is carried out by heating the coating film obtained in the step 〇) to a temperature at which the polymerizable liquid crystal compound contained in the coating film is transferred to the nematic phase In the above, the polymerizable liquid crystal compound is cooled to a temperature of the phase of the display layer to obtain a film in which the polymerizable liquid crystal compound is aligned as a film of a smectic phase; [8] a display device comprising [4] Optical film; [9] A display device comprising an optical film obtained by the manufacturing method of [5]; [10] The optical film obtained by the production method of [6] or [7] is contained. [Embodiment] In the present invention, the term "optical film" means a film that transmits light and has an optical function. The term "optical" refers to absorption, reflection, diffraction, scattering, refraction, and birefringence. A retardation film, which is one type of optical film, is used to convert linearly polarized light into circularly polarized or elliptically polarized light, or conversely converts circularly polarized or elliptically polarized light into 158656.doc 201224125 linearly polarized light. The polarizing film which is one type of optical film is used to decompose the unpolarized incident light into two orthogonal polarizing components, and to transmit one polarizing component and absorb the other polarizing component. The axial direction of the transmitted polarization component as the transmission axis is called the absorption axis. The polymerizable liquid crystal composition of the present invention contains a polymerizable liquid crystal compound exhibiting a smectic phase, a leveling agent, and a solvent, and the leveling agent is selected from a leveling agent containing a polyacrylic acid vinegar compound as a main component and a fluorine atom. The content of the leveling agent is at least 0.3 parts by mass and not more than 5 parts by mass based on 100 parts by mass of the polymerizable liquid crystal compound. The polymerizable liquid crystal compound is a compound having a polymerizable group and exhibiting liquid crystallinity. The polymerizable group means a group which participates in the polymerization reaction of the polymerizable liquid crystal compound. The polymerizable liquid crystal compound is a polymerizable liquid crystal compound which exhibits a smectic phase, and is preferably a polymerizable liquid crystal compound which exhibits a nematic phase between the temperature of the display layer and the temperature of the isotropic phase. When the polymerizable liquid crystal compound is such a compound, there is a tendency that the stratified phase of the horizontal alignment can be easily obtained. As the smectic phase, a smectic A phase, a layer (four) phase, and a smectic column are exemplified.

型D相、層列_目、層列型F相、層列型㈣、層列型H 相、層列型1相、層列型J相及層列型K相。其中,較佳為 :=、層列型F相及層列型!相,更佳為層:Type D phase, smectic _ mesh, smectic F phase, smectic type (four), smectic H phase, smectic type 1 phase, smectic J phase, and smectic K phase. Among them, it is preferably: =, smectic F phase and smectic phase! phase, more preferably layer:

=性:晶化合物顯示之液晶相為該等液晶相,則可於 付配向秩序度較高之光學膜。 X 158656.doc 201224125 作為聚合性液晶組合物,可列舉式(1)所示之化合物(以 下有時稱為「化合物(1)」)。 U^V^w^xLy^x^y^x^w^V2-!;^!) [式(1)中,X1、X2及X3表示可具有取代基之對伸苯基或可 具有取代基之環己烷-1,4-二基。其中,χ1、X2及X3中之至 少1個表示可具有取代基之對伸苯基。 Υ1及Υ2相互獨立地表示-CH2CH2- -ch2o- -COO- -〇C-或 CRa=N- _〇C〇〇_、單鍵、·Ν=Ν·、_CRa=CRb 尺3及1^相互獨立地表示氫原子或碳數i〜4之烷基。 u表示氫原子或聚合性基。 U2表示聚合性基。 W及W2相互獨立地表示單鍵、_〇·、各、弋〇〇_或 OCOO- 〇 及V2相互獨立地表示可具有取代基之碳數卜2〇之二價 烷基,且該二價烷基中所含之_CH2_亦可取代為ο、_s或 NH-] X1、X2及X3相互獨立為可具有取代基之料苯基、或可 具有取代基之環己烷-M_二基。其中,χ1、Χ1Χ3中之至 少1個表示可具有取代基之丨,4•伸笨基。 較佳為X1、X2及X3中夕5 ,丨、Α _ τ之至少2個為可具有取代基之對伸 笨基。 上述對伸苯基較佳為未經取代。上述環己H,4_二基較 佳為反式環己烷-U4-二基’該等更佳為未經取代。 作為對伸苯基所具有之取代基,可列舉:f基、乙基、 158656.doc 201224125 丁基等碳數1〜4之烷基’氰基,及氟基(氟原子)、氯基(氯 原子)、溴基(溴原子)等鹵素基(鹵原子)。 作為環己烷-1,4-二基所具有之取代基,可列舉:甲基、 乙基、丁基等碳數1〜4之烧基,氰基,及氟基(敗原子广 氣基(氣原子)、溴基(溴原子)等鹵素基(鹵原子)。環己 烧-1,4-二基之_CH2_亦可取代為_〇、_s或nr_。r為碳數 1〜6之烷基或苯基。 Y1 及 Y2相互獨立為 _CH2CH2_、_CH2〇 ' _c〇〇 、 -ocoo-、單鍵、_N=N_、_CRa=CRb …《 或 cRa=N。 該等基之鍵結位置可為任一方向。 R及R相互獨立為氫原子或碳數卜4之烷基。作為碳數 1〜4之烷基,可列舉:甲基、乙基、丁基等。 Y較佳為-CH2CH2-、-COO-或單鍵。 Y 較佳為-CH2CH2-或 CH2〇-。 U1為氫原子或聚合性基,較佳為聚合性基。心聚合性 基U及u較佳為均為光聚合性基。所謂「光聚合性 基」’係指可利用自光聚合起始劑產生之活性自由基或酸 等而參與聚合之基。 u及U較佳為相同種類之基。 作為聚合性基,可列舉:乙稀基、乙稀氧基、b氣乙稀 基、異丙稀基、4-乙烯基苯基、丙烯醯氧基、甲基丙烯醯 氧基、環氧乙烷基'環氧丙烷基等。其中,較佳為丙烯醯 158656.doc 201224125 氧基、甲基丙烯醯氧基、乙烯氧基、環氧乙烷基及環氧丙 炫•基,更佳為丙烯醯氧基。 v1及v2相互獨立為可具有取代基之碳數丨〜20之二價烷 基’該二價烷基中所含之-CH2·亦可取代為_〇_、_1或]^]9[_。 作為碳數1〜2 0之二價烧基,可列舉:亞甲基、伸乙基、 丙烷-1,3-二基、丁烷-u-二基、丁烷二基、戊烷-u- 二基、己烷·1,6-二基、庚烷q,7_二基、辛烷_18二基、癸 烷·ι,ιο-二基、十四烷_114•二基及二十烷_12〇二基等, 較佳為碳數2〜12之:價燒基,更佳為碳數6〜12之二價烧 基。 作為該_價院基所具有之取代基’可列舉4基,及敗 基⑽子)、氯基(氯原子)、漠基(漠原子)等齒素基(齒原 子)。 較佳為未經取代之二價 二價貌基。 -基’更佳為未經取代之直鏈狀 _s-、-CO-O-或-O-CO-O· W】及W2相互獨立為單鍵、·〇_ ’較佳為單鍵或_0_。 作為化合物⑴,可 物。下述式中,環…!,都21)所示之化合 基。 ’ 一基較佳為反式環己烷-1,4-二 158656.doc h<h2〇6*o= Sex: When the liquid crystal phase of the crystalline compound is such a liquid crystal phase, an optical film having a higher degree of alignment can be dispensed. X 158656.doc 201224125 The polymerizable liquid crystal composition is exemplified by a compound represented by the formula (1) (hereinafter sometimes referred to as "compound (1)"). U^V^w^xLy^x^y^x^w^V2-!;^!) [In the formula (1), X1, X2 and X3 represent a para-phenyl group which may have a substituent or may have a substituent. Cyclohexane-1,4-diyl. Among them, at least one of χ1, X2 and X3 represents a para-phenyl group which may have a substituent. Υ1 and Υ2 independently of each other -CH2CH2- -ch2o- -COO- -〇C- or CRa=N- _〇C〇〇_, single bond, ·Ν=Ν·, _CRa=CRb ruler 3 and 1^ The hydrogen atom or the alkyl group having a carbon number of i to 4 is independently represented. u represents a hydrogen atom or a polymerizable group. U2 represents a polymerizable group. W and W2 independently of each other represent a single bond, _〇·, each, 弋〇〇_ or OCOO-〇 and V2 independently of each other represent a divalent alkyl group having a carbon number of a substituent, and the divalent The _CH2_ contained in the alkyl group may also be substituted with ο, _s or NH-] X1, X2 and X3 are each independently a phenyl group which may have a substituent, or a cyclohexane-M_ which may have a substituent base. Among them, at least one of χ1, Χ1Χ3 represents a ruthenium which may have a substituent, and 4 is a stupid base. Preferably, at least two of X, Α, _ τ τ of X1, X2 and X3 are a pair of stable bases which may have a substituent. The above-mentioned para-phenylene group is preferably unsubstituted. The above cyclohexyl H,4_diyl group is preferably transcyclohexane-U4-diyl' which is more preferably unsubstituted. Examples of the substituent which the p-phenylene group has include an alkyl group having a carbon number of 1 to 4 such as an amino group, an ethyl group, a 158656.doc 201224125 butyl group, and a fluorine group (fluorine atom) or a chlorine group ( A halogen group (halogen atom) such as a chlorine atom or a bromine group (bromine atom). Examples of the substituent of the cyclohexane-1,4-diyl group include a carbon group of 1 to 4 such as a methyl group, an ethyl group, and a butyl group, a cyano group, and a fluoro group. a halogen group (halogen atom) such as a (gas atom) or a bromine group (bromine atom). The _CH2_ of the cyclohexane-1,4-diyl group may also be substituted with _〇, _s or nr_. r is a carbon number of 1~ 6 alkyl or phenyl. Y1 and Y2 are each independently _CH2CH2_, _CH2〇' _c〇〇, -ocoo-, single bond, _N=N_, _CRa=CRb ... or cRa=N. The position of the knot may be any direction. R and R are each independently a hydrogen atom or an alkyl group having a carbon number of 4. The alkyl group having 1 to 4 carbon atoms may, for example, be a methyl group, an ethyl group or a butyl group. Preferably, it is -CH2CH2-, -COO- or a single bond. Y is preferably -CH2CH2- or CH2?-. U1 is a hydrogen atom or a polymerizable group, preferably a polymerizable group. The core polymerizable groups U and u are preferably. The term "photopolymerizable group" means a group which can participate in polymerization by using an active radical derived from a photopolymerization initiator or an acid, etc. U and U are preferably the same type of group. As the polymerizable group, a vinyl group can be cited. Ethyleneoxy, b-ethylene, isopropyl, 4-vinylphenyl, acryloxy, methacryloxy, oxiranyl epoxide, etc.为 is acryl 醯 158656.doc 201224125 oxy, methacryloxyloxy, ethyleneoxy, oxiranyl and epoxihydryl groups, more preferably propylene oxime. v1 and v2 are independent of each other. The divalent alkyl group having a carbon number of 丨~20 having a substituent '-CH2· contained in the divalent alkyl group may be replaced by _〇_, _1 or ]^]9[_. As the carbon number 1 to 2 The divalent alkyl group of 0 may, for example, be a methylene group, an ethyl group, a propane-1,3-diyl group, a butane-u-diyl group, a butanediyl group, a pentane-u-diyl group, or a hexane. · 1,6-diyl, heptane q,7-diyl, octane-18 diyl, decane·ι, ιο-diyl, tetradecane_114•diyl and eicosane_12〇 The base or the like is preferably a carbon number of 2 to 12: a valent group, more preferably a divalent alkyl group having a carbon number of 6 to 12. As a substituent of the valence group, four bases can be cited, and A dentate group (a tooth atom) such as a group (10)), a chlorine group (chlorine atom), or a desert group (a desert atom). Preferred is an unsubstituted divalent divalent base. - The base 'better is unsubstituted linear _s-, -CO-O- or -O-CO-O · W] and W2 are independent of each other as a single bond, 〇 _ ' prefers a single bond or _0_. As the compound (1), it is an object. In the following formula, the ring...! , all of the compounds shown in 21). ' One base is preferably trans cyclohexane-1,4-two 158656.doc h<h2〇6*o

〇iCH2)6 o ^(HaCJn (H2〇)6〇iCH2)6 o ^(HaCJn (H2〇)6

(CH2)6 201224125 3-^H2c)6-〇H〇^"^^^〇-〇i〇H2>6o-^ 3·^Η2〇)β·〇Η〇^〇'^^〇·ο~〇-(^Η2)6〇-ζ= 〇-(ch2)6〇^ %(CH2)6 201224125 3-^H2c)6-〇H〇^"^^^〇-〇i〇H2>6o-^ 3·^Η2〇)β·〇Η〇^〇'^^〇·ο ~〇-(^Η2)6〇-ζ=〇-(ch2)6〇^ %

3"°(h2cv〇-〇^^>o- 〇-(CH2)8H o-t 3^0 '(H2C)ii-〇 C6H13^0-O>^<^^〇-〇^(CH2)6-°^ -Ohd〉-陶! r〇 七 o (M) (1-2) (1-3) (1-4) (1-5) (1-6) α-7) α-8) (1-9) (1,10) (MI) 201224125 qH2〇)6·3"°(h2cv〇-〇^^>o- 〇-(CH2)8H ot 3^0 '(H2C)ii-〇C6H13^0-O>^<^^〇-〇^(CH2)6 -°^ -Ohd〉-陶! r〇七o (M) (1-2) (1-3) (1-4) (1-5) (1-6) α-7) α-8) ( 1-9) (1,10) (MI) 201224125 qH2〇)6·

-(CH2&gt;6 I (1-12) (M3) (1-14) (1.15) (1-16) (1-17) (1-18) (1-19) (1-20) α-2ΐ) P-t s3&quot;〇&lt;h2c&gt;6-0O~0;^w^^O&quot;0&quot;&lt;ch2)60 七 3-〇(H2c}6-〇Omd^〇&quot;0^Q-〇&lt;CH2)6o( 3^&lt;H2C&gt;6*〇^^〇&quot;H^〇,L~0K^&lt;&lt;^2)6〇·^ 3~°(鳴〇 3^H2C)6-〇O~^〈H)-〇-〇-(CH2)e〇 尤 &gt;^·〇·〇·^0^〇 傳 H(H2C)e-〇-(CH2&gt;6 I (1-12) (M3) (1-14) (1.15) (1-16) (1-17) (1-18) (1-19) (1-20) α-2ΐ ) Pt s3&quot;〇&lt;h2c&gt;6-0O~0;^w^^O&quot;0&quot;&lt;ch2)60 七3-〇(H2c}6-〇Omd^〇&quot;0^Q-〇&lt; CH2)6o( 3^&lt;H2C&gt;6*〇^^〇&quot;H^〇,L~0K^&lt;&lt;^2)6〇·^ 3~°(〇3^H2C)6-〇 O~^<H)-〇-〇-(CH2)e〇尤&gt;^·〇·〇·^0^〇传H(H2C)e-〇

3^〇(H2C)6-〇-〇^~&lt;^^〇-〇-〇-(CH2)eH H(H2CV〇-0^{^b-O~〇-(CH2)6O 尤 化合物(1)之含量相對於聚合性液晶組合物之固形物成 分100質量%,較佳為70〜99.9質量%,更佳為90~99.9質量 %。若為上述範圍内,則有化合物之配向性變高之傾向。 本說明書中,所謂「固形物成分」,係指聚合性液晶組合 物之全部成分中除溶劑以外之成分。亦可使用兩種以上之 化合物U)。 •10· 158636.doc3^〇(H2C)6-〇-〇^~&lt;^^〇-〇-〇-(CH2)eH H(H2CV〇-0^{^bO~〇-(CH2)6O Compound (1) The content is preferably from 70 to 99.9% by mass, more preferably from 90 to 99.9% by mass, based on 100% by mass of the solid content of the polymerizable liquid crystal composition. If it is within the above range, the alignment of the compound tends to be high. In the present specification, the "solid content component" means a component other than the solvent in all the components of the polymerizable liquid crystal composition. Two or more compounds U) may be used. •10· 158636.doc

201224125 調平劑係選自由以聚丙烯酸酯化合物為主成分之調平劑 及以含氟原子之化合物為主成分之調平劑所組成之群中之 至少1種。所謂調平劑,係指具有調整聚合性液晶組合物 之流動性,使塗佈之膜變得平坦之功能者,可列舉界面活 性劑等。 作為以聚丙烯酸酯化合物為主成分之調平劑,可列舉: ΒΥΚ-350、ΒΥΚ-352、ΒΥΚ-353、ΒΥΚ-354、BYK-355、 BYK-358N、BYK-361N、BYK-380、BYK-381、BYK-392 (均為商品名,BYK Chemie公司製造)等。 作為以含氟原子之化合物為主成分之調平劑,可列舉: Megafac(商品名)R-08、Megafac R-30、Megafac R-90、 Megafac F-410 ' Megafac F-411 ' Megafac F-443 ' Megafac F-445、Megafac F-470、Megafac F-471、Megafac F-477、 Megafac F-479、Megafac F-482、Megafac F-483(以上,均 為 DIC(股)製造),Surflon(商品名)S-381、Surflon S-382、 Surflon S-383、Surflon S-393、Surflon SC-101 ' Surflon SC-105、KH-40、SA-100(以上,均為 AGC Seimi Chemical(股)製造),商品名E1830、商品名E5844 ((股)Daikin Fine Chemical 研究所製造),Eftop(商品 名)EF301、Eftop EF303、Eftop EF351、Eftop EF352(以 上,均為Mitsubishi Materials Electronic Chemicals(股)製 造)等。 調平劑之含量相對於聚合性液晶化合物100質量份,為 0.3質量份以上且5質量份以下,較佳為0.5質量份以上且3 158656.doc 201224125 質量份以下。若調平劑之含量為上述之範圍内,則易使聚 合性液晶組合物中所含之成分水平配向,且有所得之光學 膜變平滑之傾向。若調平劑之含量超過5質量份,則於所 得之光學膜上容易產生不均。該等調平劑可使用選自由以 聚丙烯酸酯化合物為主成分之調平劑及以含氟原子之化合 物為主成分之調平劑所組成之群中之丨種以上,亦可併用2 種以上。 調平劑較佳為聚丙烯酸酯化合物、含氟原子之化合物或 該專兩者。 本發明之聚合性液晶組合物較佳為含有二色性色素❶若 本發明之聚合性液晶組合物含有二色性色素,則所得之光 學膜具有作為偏光膜之功能。所謂二色性色素,係指具有 分子之長軸方向上之吸光度與短軸方向上之吸光度不同之 性質的色素。 二色性色素可為染料’亦可為顏料。作為二色性色素, 較佳為於300〜700 nm之範圍内具有極大吸收波長之二色性 色素J作為二色性色素,可列舉…定色素…井色 素化月色素、萘色素、偶氮色素及葱酿色素。亦可組合 使用兩種以上之二色性色素。 口 二色性色素較佳為偶氮色素。作為偶氮色素,可列舉· 單偶氮色素、雙偶氮色素、三偶氮色素、四偶氮色素及甚 偶氮色素,較佳為雙偶氮色素及三偶氮色素。 作為偶氮色素,可列舉式(2)所示之化合物。 A ,(-Ν=Ν-Α2)ρ-Ν=Ν-Α3(2) 158656.doc -12- 201224125 [式(2)中,A1及A3分別獨立地表示可具有取代基之笨基、 可具有取代基之萘基或可具有取代基之!價雜環基;A2分 別獨立地表示可具有取代基之對伸笨基、可具有取代基之 萘-1,4-二基或可具有取代基之2價雜環基;p表示之整 數;於P為2以上之整數之情形時,複數個a2可分別相同, 亦可不同] 作為1價雜環基’可列舉自喹啉環、噻唑環、苯并嗟嗤 環、噻吩幷噻唑環、咪唑環、苯并咪唑環、嘮唑環、苯并 坐環專雜環上去除1個氫原子而成之基。又,作為2價雜 環基,可列舉自上述雜環上去除2個氫原子而成之基。 作為A1及A3中之苯基、萘基及1價雜環基、以及a2中之 對伸苯基、萘-1,4-二基及2價雜環基所具有之取代基,可 列舉:曱基、乙基、丁基等碳數之烷基;甲氡基、乙 氧基、丁氧基等碳數1〜4之烷氧基;三氟甲基等碳數1〜4之 良化烷基;氰基;硝基;氟基、氣基、溴基等南素基;胺 基;二乙胺基、吡咯烷基等經碳數1〜4之烷基取代之胺基 (取代在胺基上之2個烷基亦可相互鍵結而形成碳數2〜8之 一價统基)。 作為偶氮色素,較佳為下述式(2-1)〜(2-6)所示之化合 物。 158656.doc 13- 201224125 N=N-·^^—Ν=Ν· .B2 J nl201224125 The leveling agent is at least one selected from the group consisting of a leveling agent containing a polyacrylate compound as a main component and a leveling agent containing a fluorine atom-containing compound as a main component. The leveling agent is a function of adjusting the fluidity of the polymerizable liquid crystal composition and flattening the applied film, and examples thereof include a surfactant. As a leveling agent containing a polyacrylate compound as a main component, ΒΥΚ-350, ΒΥΚ-352, ΒΥΚ-353, ΒΥΚ-354, BYK-355, BYK-358N, BYK-361N, BYK-380, BYK -381, BYK-392 (all trade names, manufactured by BYK Chemie Co., Ltd.), etc. As a leveling agent containing a fluorine atom-containing compound as a main component, Megafac (trade name) R-08, Megafac R-30, Megafac R-90, Megafac F-410 ' Megafac F-411 ' Megafac F- 443 ' Megafac F-445, Megafac F-470, Megafac F-471, Megafac F-477, Megafac F-479, Megafac F-482, Megafac F-483 (all above, manufactured by DIC), Surflon ( Trade name) S-381, Surflon S-382, Surflon S-383, Surflon S-393, Surflon SC-101 ' Surflon SC-105, KH-40, SA-100 (above, all AGC Seimi Chemical) Manufactured under the trade name E1830, trade name E5844 (manufactured by Daikin Fine Chemical Research Institute), Eftop (trade name) EF301, Eftop EF303, Eftop EF351, Eftop EF352 (above, all manufactured by Mitsubishi Materials Electronic Chemicals) )Wait. The content of the leveling agent is 0.3 parts by mass or more and 5 parts by mass or less, preferably 0.5 parts by mass or more and 3 158656.doc 201224125 parts by mass or less based on 100 parts by mass of the polymerizable liquid crystal compound. When the content of the leveling agent is within the above range, the components contained in the polymerizable liquid crystal composition tend to be aligned horizontally, and the obtained optical film tends to be smooth. When the content of the leveling agent exceeds 5 parts by mass, unevenness easily occurs in the obtained optical film. The leveling agent may be one selected from the group consisting of a leveling agent containing a polyacrylate compound as a main component and a leveling agent containing a fluorine atom-containing compound as a main component, or two types may be used in combination. the above. The leveling agent is preferably a polyacrylate compound, a fluorine atom-containing compound or both. The polymerizable liquid crystal composition of the present invention preferably contains a dichroic dye. If the polymerizable liquid crystal composition of the present invention contains a dichroic dye, the obtained optical film functions as a polarizing film. The dichroic dye refers to a dye having a property in which the absorbance in the long axis direction of the molecule is different from the absorbance in the short axis direction. The dichroic dye can be a dye or a pigment. The dichroic dye is preferably a dichroic dye J having a maximum absorption wavelength in the range of 300 to 700 nm as a dichroic dye, and examples thereof include a pigmentation dye, a naphthol pigment, a naphthalene pigment, and an azo. Pigment and onion brewing pigments. It is also possible to use two or more kinds of dichroic dyes in combination. The dichroic dye is preferably an azo dye. Examples of the azo dye include a monoazo dye, a disazo dye, a trisazo dye, a tetrazo pigment, and a azo dye, and a disazo dye and a trisazo dye are preferable. The azo dye is a compound represented by the formula (2). A , (-Ν=Ν-Α2)ρ-Ν=Ν-Α3(2) 158656.doc -12- 201224125 [In the formula (2), A1 and A3 each independently represent a stupid group which may have a substituent, A naphthyl group having a substituent or may have a substituent! a heterocyclic group; A2 each independently represents a diastereous group which may have a substituent, a naphthalene-1,4-diyl group which may have a substituent or a divalent heterocyclic group which may have a substituent; p represents an integer; When P is an integer of 2 or more, a plurality of a2 may be the same or different, and the monovalent heterocyclic group may be exemplified by a quinoline ring, a thiazole ring, a benzofluorene ring, a thiophene thiazole ring, or the like. The imidazole ring, the benzimidazole ring, the carbazole ring, and the benzo ring-shaped heterocyclic ring are formed by removing one hydrogen atom. Further, examples of the divalent heterocyclic group include a group obtained by removing two hydrogen atoms from the above heterocyclic ring. Examples of the substituent of the phenyl group, the naphthyl group and the monovalent heterocyclic group in A1 and A3, and the para-phenyl group, naphthalene-1,4-diyl group and divalent heterocyclic group in a2 include: An alkyl group having a carbon number such as a mercapto group, an ethyl group or a butyl group; an alkoxy group having a carbon number of 1 to 4 such as a mercapto group, an ethoxy group or a butoxy group; and a melamine having a carbon number of 1 to 4 such as a trifluoromethyl group; An alkyl group; a cyano group; a nitro group; a fluoro group, a gas group, a bromo group, and the like; an amine group; a diethylamino group, a pyrrolidinyl group, and the like substituted with an alkyl group having 1 to 4 carbon atoms (substituted in The two alkyl groups on the amine group may also be bonded to each other to form a carbon number of 2 to 8 ones. The azo dye is preferably a compound represented by the following formulas (2-1) to (2-6). 158656.doc 13- 201224125 N=N-·^^—Ν=Ν· .B2 J nl

(2-3)(2-3)

1==N^Q^B12 (2-1) B7 (2-2) (M)1==N^Q^B12 (2-1) B7 (2-2) (M)

(2-5)(2-5)

(2r6) [式(2-1)〜(2_6)中’ B1〜B20分別獨立地表示氫原子、碳數 1〜4之烷基、碳數1〜4之烷氧基、氰基、硝基、胺基、經碳 數1〜4之烧基取代之胺基(取代在胺基上之2個烷基亦可相 互鍵結而形成碳數2〜8之二價烷基)、氣基(氯原子)或三氟 甲基;η 1〜n4分別獨立地表示〇〜3之整數] 作為葱醌色素,較佳為式(2_7)所示之化合物。 R8 Ο R1(2r6) [B1 to B20 in the formulae (2-1) to (2_6) independently represent a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, and a nitro group. An amine group, an amine group substituted with a carbon group of 1 to 4 (the two alkyl groups substituted on the amine group may be bonded to each other to form a divalent alkyl group having 2 to 8 carbon atoms), and a gas group ( Chlorine atom) or trifluoromethyl group; η 1 to n4 each independently represent an integer of 〇 3 to 3] As the onion pigment, a compound represented by the formula (2-7) is preferable. R8 Ο R1

R2 R3 (2-7) 14· 158656.docR2 R3 (2-7) 14· 158656.doc

201224125 -Rx、胺基、 [式(2-7)中,Ri〜R8分別獨立地表*氫原子201224125 -Rx, amine group, [in formula (2-7), Ri~R8 are independently represented by a hydrogen atom

Rx表示碳數1〜4之烧基或 -NHRX、-NR、、_叱或 _原子 碳數6〜12之芳基] 作為W色素,較佳為式(2_8)所示之化合物Rx represents a carbon group having 1 to 4 carbon atoms or -NHRX, -NR, _叱 or _ atom, and an aryl group having 6 to 12 carbon atoms. As the W coloring matter, a compound represented by the formula (2-8) is preferred.

[式(2-7)中’ R〜RU分別獨立地表示氫原子、_RX、胺 基NHR、-NR 2、-81^或_原子,Rx表示碳數卜4之烷 基或碳數6〜12之芳基] 作為啰酮色素,較佳為式(2_9)所示之化合物。[In the formula (2-7), R to RU independently represent a hydrogen atom, _RX, an amine group NHR, -NR 2, -81^ or _ atom, and Rx represents an alkyl group of carbon number 4 or a carbon number of 6~ Aryl group of 12] As the anthrone dye, a compound represented by the formula (2-9) is preferred.

[式(2-9)中’ R9〜RM分別獨立地表示氳原子、_rX、胺 基、-NHR、-NR 2、_SRX或函原子,Rx表示碳數卜4之炫 基或碳數6〜12之芳基] 作為Rx中之碳數1〜4之烷基,可列舉:甲基、乙基、丙 基及丁基。 作為Rx中之碳數6〜12之芳基,可列舉:苯基、曱苯基、 二曱苯基及萘基。 作為花青色素,較佳為式(2-1〇)所示之化合物及式(2_u) 158656.doc ,, 201224125 所示之化合物。 D1~h^^2 (mo[In the formula (2-9), 'R9 to RM each independently represent a ruthenium atom, _rX, an amine group, -NHR, -NR 2, _SRX or a functional atom, and Rx represents a condensed group of carbon number 4 or a carbon number of 6~ Aryl group of 12] The alkyl group having 1 to 4 carbon atoms in Rx may, for example, be a methyl group, an ethyl group, a propyl group or a butyl group. Examples of the aryl group having 6 to 12 carbon atoms in Rx include a phenyl group, a fluorenylphenyl group, a diphenylene group, and a naphthyl group. The cyanine dye is preferably a compound represented by the formula (2-1) and a compound represented by the formula (2_u) 158656.doc, 201224125. D1~h^^2 (mo

Jn5 [式(2*~1〇)中,·ρ^ U及0分別獨立地表示式(2-10a)〜式(2-10d) 所示之基;Jn5 [In the formula (2*~1〇), ρ^ U and 0 respectively represent the groups represented by the formula (2-10a) to the formula (2-10d);

d^=c-c==D4 (2.n) l J n6d^=c-c==D4 (2.n) l J n6

C-10d) [式(2-11)中’ D3及D4分別獨立地表示式(2_lla)〜式(2_uh) 所示之基; ===ζ〇 ^x) (2-lla&gt; (2-11b) (2-lic) (211d)C-10d) [In the formula (2-11), 'D3 and D4 each independently represent a group represented by the formula (2_lla) to the formula (2_uh); ===ζ〇^x) (2-lla&gt; (2- 11b) (2-lic) (211d)

n6表示1〜3之整數j 二色性色素之含量相對於聚合性液晶化合物1〇〇質量 158656.docN6 represents an integer of 1 to 3 j. The content of the dichroic dye relative to the mass of the polymerizable liquid crystal compound 158656.doc

-16 - 201224125 伤車又佳為50質量份以下,更佳為o.l質量份以上且20質 量伤以下,更佳為〇. 1質量份以上且10質量份以下。若為 上述範圍內,Hil 貝】可不擾亂聚合性液晶化合物之配向而進行 聚合°右一色性色素之含量超過50質量份,則有擾亂聚合 性液晶化合物之配向之虞,故而不佳。 作為溶劑’較佳為可溶解聚合性液晶組合物之各成分的 /合齊丨又’較佳為對聚合性液晶組合物之聚合反應為惰性 之溶劑。 作為溶劑,可列舉:甲醇 '乙醇、乙二醇、異丙醇、丙 一醇乙一醇甲基醚、乙二醇丁基醚、丙二醇單曱基醚等 醇冷劑’乙酸乙酯、乙酸丁酯、乙二醇曱基醚乙酸酯、 丁内Sa、丙一醇曱基醚乙酸酯、乳酸乙酯等酯溶劑,丙 酮、曱基乙基酮、環戊酮、環己酮、2_庚酮、甲基異丁基 銅等酮洛劑,戊院、己烧、庚燒等脂肪族煙溶劑,甲苯、 二甲苯等芳香族烴溶劑’乙腈等腈溶劑,四氫呋喃、二曱 氧基乙烧等㈣劑,及氯仿' 氣料含氣溶劑。該等溶劑 可單獨使用’亦可組合使用兩種以上。 溶劑之含量相對於聚合性液晶組合物總量,較佳為 質量%。若溶劑為98質量%以下,則由聚合性液晶組 合物所得之光學膜之膜厚不會變得過薄,可容易地獲得具 有作為光學膜所需之特性的光學膜。若溶劑為5〇質量%以 上,則有聚合性液晶組合物之黏度較低,變得不易於塗膜 之膜厚上產生不均之傾向。 本發明之聚合性液晶組合物亦可含有聚合起始劑。聚合 158656.doc •17· 201224125 起始劑係開始聚合性液晶化合物之聚合反應的化合物,其 藉由光及/或熱之作用而產生活性自由基或酸。其中,較 佳為藉由光之作用而產生活性自由基或酸之聚合起始劑、 即光聚合起始劑’更佳為藉由光照射而產生自由基之光聚 合起始劑。 作為光聚合起始劑,可列舉:安息香化合物'二苯甲酮 化合物、烷基苯酮化合物、醯基氧化膦化合物、三畊化合 物、錤鹽及銃鹽。 作為安息香化合物,可列舉:安息香、安息香甲基醚、 安息香乙基醚、安息香異丙基醚及安息香異丁基醚。 作為二苯曱_化合物’可列舉:二苯曱酮、鄰苯甲醯基 苯甲酸甲酯、4-苯基二苯曱酮、4-苯曱醯基-4·-甲基二苯硫 謎、3,3’,4,4'-四(第三丁基過氧化羰基)二苯甲酮及2,4,6_三 甲基二苯甲酮。 作為烧基苯酮化合物,可列舉:二乙氧基苯乙酮、2-甲 基-2-嗎啉基_ι_(4-曱基噻吩基)丙烷-1-酮、2-苄基-2-二甲 胺基-1-(4-嗎啉基苯基)丁烷-i_酮、2-羥基-2·甲基-1-苯基 丙烷-1-酮、1,2_二苯基-2,2-二曱氧基乙烷-1-酮、2-羥基 -2-甲基-l-[4-(2-羥基乙氧基)苯基]丙烷-1-酮、1-羥基環己 基苯基酮及2-羥基-2-曱基- l-[4-(l -甲基乙烯基)苯基]丙 烧1 -酮之低聚物。 作為醯基氧化膦化台物,可列舉:2,4,6-三甲基苯甲醯 基二苯基氧化膦及雙(2,4,6-三曱基苯甲醯基)苯基氧化膦。 作為三畊化合物,可列舉:2,4-雙(三氣甲基)-6-(4-甲氧 158656.doc -18 - 201224125 基苯基)-1,3,5 -三p井、2,4 -雙(三氯甲基)-6-(4-甲氧基蔡 基)-1,3,5-三。井、2,4-雙(三氣甲基)-6-(4-甲氧基苯乙烯基) -1,3,5-三*»井、2,4-雙(三氯甲基)-6-[2-(5-甲基0夫0南-2-基)乙 烯基]-1,3,5-三畊、2,4-雙(三氣甲基)-6-[2-(呋喃-2-基)乙烯 基]-1,3,5-三畊、2,4-雙(三氣曱基)-6-[2-(4-二乙胺基-2-曱 基苯基)乙烯基]-1,3,5-三畊及2,4-雙(三氣甲基)-6-[2-(3,4-二曱氧基苯基)乙烯基]-1,3,5·三畊》 作為光聚合起始劑,亦可使用:Irgacure 907、Irgacure 184 ' Irgacure 651 ' Irgacure 819 ' Irgacure 250 ' Irgacure 369(以上’均為 Ciba.Japan(股)製造),Seikuol BZ、 Seikuol Z、Seikuol BEE(以上,均為精工化學(股)製造),-16 - 201224125 The injured car is preferably 50 parts by mass or less, more preferably 0.1 parts by mass or more and 20 parts or less, more preferably 1 part by mass or more and 10 parts by mass or less. In the above range, Hil can be polymerized without disturbing the alignment of the polymerizable liquid crystal compound. When the content of the right-color dye exceeds 50 parts by mass, the alignment of the polymerizable liquid crystal compound is disturbed, which is not preferable. The solvent 'is preferably a solvent which dissolves the components of the polymerizable liquid crystal composition, and is preferably a solvent which is inert to the polymerization reaction of the polymerizable liquid crystal composition. Examples of the solvent include alcohol refrigerants such as methanol 'ethanol, ethylene glycol, isopropyl alcohol, propanol ethyl alcohol methyl ether, ethylene glycol butyl ether, and propylene glycol monodecyl ether. Ester, ethylene glycol decyl ether acetate, butane Sa, propanol decyl ether acetate, ester solvent such as ethyl lactate, acetone, mercaptoethyl ketone, cyclopentanone, cyclohexanone, 2 Ketone ketones such as heptanone and methyl isobutyl copper, aliphatic ketone solvents such as pentyl, hexanol and gamma, aromatic hydrocarbon solvents such as toluene and xylene, nitrile solvents such as acetonitrile, tetrahydrofuran and dimethoxyl Ethylene (etc.), and chloroform's gas-containing solvent. These solvents may be used singly or in combination of two or more. The content of the solvent is preferably % by mass based on the total amount of the polymerizable liquid crystal composition. When the amount of the solvent is 98% by mass or less, the film thickness of the optical film obtained from the polymerizable liquid crystal composition does not become too thin, and an optical film having characteristics required as an optical film can be easily obtained. When the amount of the solvent is 5% by mass or more, the viscosity of the polymerizable liquid crystal composition is low, and the film thickness of the coating film tends to be uneven. The polymerizable liquid crystal composition of the present invention may further contain a polymerization initiator. Polymerization 158656.doc • 17· 201224125 The initiator is a compound which initiates polymerization of a polymerizable liquid crystal compound, which generates an active radical or an acid by the action of light and/or heat. Among them, a photopolymerization initiator which is a polymerization initiator which generates an active radical or an acid by the action of light, that is, a photopolymerization initiator is more preferably a photopolymerization initiator which generates a radical by light irradiation. The photopolymerization initiator may, for example, be a benzoin compound, a benzophenone compound, an alkylphenone compound, a mercaptophosphine oxide compound, a tri-enriched compound, an onium salt or a phosphonium salt. As the benzoin compound, benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, and benzoin isobutyl ether can be mentioned. Examples of the diphenyl hydrazine-compounds include: benzophenone, methyl ortho-benzoylbenzoate, 4-phenyldibenzophenone, 4-phenylmercapto-4·-methyldiphenyl sulfide 3,3',4,4'-tetra(t-butylperoxycarbonyl)benzophenone and 2,4,6-trimethylbenzophenone. Examples of the alkyl benzophenone compound include diethoxyacetophenone, 2-methyl-2-morpholinyl_ι-(4-mercaptothienyl)propan-1-one, and 2-benzyl-2. - dimethylamino-1-(4-morpholinylphenyl)butane-i-ketone, 2-hydroxy-2.methyl-1-phenylpropan-1-one, 1,2-diphenyl -2,2-dimethoxyoxyl-1-one, 2-hydroxy-2-methyl-l-[4-(2-hydroxyethoxy)phenyl]propan-1-one, 1-hydroxyl An oligomer of cyclohexyl phenyl ketone and 2-hydroxy-2-indolyl l-[4-(1-methylvinyl)phenyl]propanone 1-one. As the fluorenylphosphine oxide substrate, 2,4,6-trimethyl benzhydryldiphenylphosphine oxide and bis(2,4,6-trimercaptobenzylidene)phenyl oxide are exemplified. phosphine. As the three-till compound, 2,4-bis(trimethylmethyl)-6-(4-methoxy 158656.doc -18 - 201224125 phenyl)-1,3,5-three p well, 2 , 4-bis(trichloromethyl)-6-(4-methoxytaryl)-1,3,5-tri. Well, 2,4-bis(trimethylmethyl)-6-(4-methoxystyryl)-1,3,5-tri*» well, 2,4-bis(trichloromethyl)- 6-[2-(5-Methyl-Of0-nan-2-yl)vinyl]-1,3,5-three tillage, 2,4-bis(trismethyl)-6-[2-( Furan-2-yl)vinyl]-1,3,5-three tillage, 2,4-bis(trimethylsulfonyl)-6-[2-(4-diethylamino-2-mercaptophenyl) )vinyl]-1,3,5-three tillage and 2,4-bis(trismethyl)-6-[2-(3,4-didecyloxyphenyl)vinyl]-1,3 , 5·3. The photopolymerization initiator can also be used: Irgacure 907, Irgacure 184 ' Irgacure 651 ' Irgacure 819 ' Irgacure 250 ' Irgacure 369 (above 'all manufactured by Ciba. Japan), Seikuol BZ , Seikuol Z, Seikuol BEE (above, all manufactured by Seiko Chemical Co., Ltd.),

Kayacure BP100(日本化藥(股)製造)、Kayacure UVI-6992 (Dow公司製造),Adeka Optomer SP-152或 Adeka Optomer SP-170(以上’均為ADEKA(股)製),TAZ-A、TAZ-PP(以 上,均為日本Siber Hegner公司製造)及TAZ_1〇4(Sanwa Chemical公司製造)等市售之光聚合起始劑。 作為熱聚合起始劑,可列舉:偶氮雙異丁腈等偶氮化合 物及過氧化氫、過硫酸鹽、過氧化笨甲醯等過氧化物。 聚合起始劑之含量相對於聚合性液晶化合物丨〇 〇質量 份,較佳為0.1〜30質量份,更佳為〇 5〜1〇質量份,更佳為 〇·5〜8質量份。若為上述範圍内,則可不擾亂聚合性液晶 化合物之配向而使之聚合。 於使用光聚合起始劑作為聚合起始劑之情形時,亦可併 用光敏劑。作為光敏劑’可列舉:仙酮,酮等,山酮化 158656.doc -19- 201224125 合物(例如2,4·二乙基噻噸酮、2·異丙基噻噸酮等)、蒽、 含炫氧基之蒽(例如二丁氧基蒽等)等蒽化合物、吩噻畊及 紅螢烯》 藉由使用光敏劑,可使聚合性液晶化合物之聚合高感度 化。光敏劑之使用量相對於聚合性液晶化合物1〇〇質量 份,較佳為0.1〜30質量份,更佳為0 5〜10質量份,更佳為 0.5〜8質量份。 本發明之聚合性液晶組合物亦可含有聚合抑制劑。藉由 使本發明之聚合性液晶組合物含有聚合抑制劑,變得容易 抑制聚合性液晶化合物之聚合,可提高本發明之聚合性液 晶組合物之穩定性。 作為聚合抑制劑,可列舉:對苯二酚、含烧氧基之對苯 二酚、含烷氧基之鄰苯二酚(例如丁基鄰苯二酚等)、鄰苯 三紛、2,2,6,6-四曱基·1_哌啶氧基自由基等自由基捕獲 劑、苯硫酚類、β-萘胺類及β-萘酚類。 聚合抑制劑之含量相對於聚合性液晶化合物1〇〇質量 份’較佳為0.1〜30質量份,更佳為〇.5〜1〇質量份,更佳為 0.5〜8質量份。若為上述範圍内,則可不擾亂聚合性液晶 化合物之配向而使之聚合。 本發明之光學膜係藉由使本發明之聚合性液晶組合物中 所含之聚合性液晶化合物聚合而獲得。 本發明之光學膜可藉由包括下述步驟(1)、步驟(2)及步 驟(3)之方法而製造。 步驟(1):將本發明之聚合性液晶組合物塗佈於基板上而獲 lS8656.doc -20-Kayacure BP100 (manufactured by Nippon Kayaku Co., Ltd.), Kayacure UVI-6992 (manufactured by Dow Co., Ltd.), Adeka Optomer SP-152 or Adeka Optomer SP-170 (all of which are manufactured by ADEKA Co., Ltd.), TAZ-A, TAZ -PP (above, all manufactured by Siber Hegner Co., Ltd.) and TAZ_1〇4 (manufactured by Sanwa Chemical Co., Ltd.) and other commercially available photopolymerization initiators. The thermal polymerization initiator may, for example, be an azo compound such as azobisisobutyronitrile or a peroxide such as hydrogen peroxide, persulfate or benzoic acid. The content of the polymerization initiator is preferably 0.1 to 30 parts by mass, more preferably 5 to 1 part by mass, even more preferably 5 to 8 parts by mass, per part by mass of the polymerizable liquid crystal compound. When it is in the above range, it can be polymerized without disturbing the alignment of the polymerizable liquid crystal compound. When a photopolymerization initiator is used as the polymerization initiator, a photosensitizer may be used in combination. Examples of the photosensitizer include: ketone, ketone, etc., ketone 158656.doc -19-201224125 (for example, 2,4·diethylthioxanthone, 2·isopropylthioxanthone, etc.), hydrazine An anthracene compound such as a fluorene-containing oxime (for example, dibutyloxyanthracene), phenothiazine, and erythrinene can improve the polymerization sensitivity of the polymerizable liquid crystal compound by using a photosensitizer. The amount of the photosensitizer to be used is preferably 0.1 to 30 parts by mass, more preferably 0 5 to 10 parts by mass, still more preferably 0.5 to 8 parts by mass, per part by mass of the polymerizable liquid crystal compound. The polymerizable liquid crystal composition of the present invention may further contain a polymerization inhibitor. When the polymerizable liquid crystal composition of the present invention contains a polymerization inhibitor, polymerization of the polymerizable liquid crystal compound can be easily suppressed, and the stability of the polymerizable liquid crystal composition of the present invention can be improved. Examples of the polymerization inhibitor include hydroquinone, alkoxybenzene-containing hydroquinone, alkoxy-containing catechol (for example, butyl catechol, etc.), ortho-benzotriene, and 2, A radical scavenger such as 2,6,6-tetradecyl·1_piperidinyloxy radical, thiophenol, β-naphthylamine and β-naphthol. The content of the polymerization inhibitor is preferably 0.1 to 30 parts by mass, more preferably 0.5 to 1 part by mass, even more preferably 0.5 to 8 parts by mass, per 1 part by mass of the polymerizable liquid crystal compound. When it is in the above range, it can be polymerized without disturbing the alignment of the polymerizable liquid crystal compound. The optical film of the present invention is obtained by polymerizing a polymerizable liquid crystal compound contained in the polymerizable liquid crystal composition of the present invention. The optical film of the present invention can be produced by a method comprising the following steps (1), (2) and (3). Step (1): applying the polymerizable liquid crystal composition of the present invention to a substrate to obtain lS8656.doc -20-

201224125 得塗佈膜之步驟 步驟(2):於步驟(1)中獲得之塗佈膜中形成液晶相之步驟 步驟(3):藉由使步驟(2)中獲得之形成有液晶相之膜中所 含之聚合性液晶化合物聚合而獲得光學膜之步驟 作為對基板之塗佈方法’可列舉:擠出塗佈法、直接凹 版塗佈法、反向凹版塗佈法、CAP塗佈法、模塗法、$ . * /¾塗 法、棒式塗佈法及旋轉塗佈法。 作為基板,可列舉玻璃、塑膠片、塑膠膜及透光性膜。 作為透光性膜’可列舉:聚乙烯、聚丙烯、降冰片稀系聚 合物等聚烯烴膜,聚乙烯醇膜、聚對苯二甲酸乙二醋膜、 聚甲基丙烯酸酯膜、聚丙烯酸酯膜、纖維素酯膜、聚蔡二 甲酸乙二酯膜、聚碳酸酯膜、聚颯膜、聚醚砜膜、聚醚酮 膜、聚苯硫醚膜及聚苯醚膜。 藉由使用基板,可於製造、搬運或保管光學膜時無發生 破損等而容易地操作。 於本發明之光學膜之製造方法中,較佳為於基板上形成 有配向膜。於此情形時,本發明之聚合性液晶組合物係塗 佈於配向膜上。配向膜較佳為具有不會因本發明之聚合性 液晶組合物之塗佈等而溶解之溶劑耐性。又,較佳為具有 用於進行溶劑之去除或液晶之配向之加熱處理中之财熱 性。進而,較佳為不產生由摩擦等所引起之剝離等之配向 膜。作為上述配向膜,較佳為包含配向性聚合物或含有配 向性聚合物之組合物。 作為上述配向性聚合物, .^ J j列舉.分子内具有醯胺鍵之 1.58656.doc •21- 201224125 聚醯胺或明膠類、分子内具有醯亞胺鍵之聚醯亞胺及作為 其水解物之聚醯胺酸、聚乙烯醇、烷基改質聚乙烯醇、聚 丙稀醯胺、聚噚唑、聚乙烯亞胺、聚苯乙烯、聚乙烯基吡 d各烧酮、聚丙烯酸、聚丙烯酸酯類等聚合物。其中,較佳 為聚乙烯醇。該等聚合物可單獨使用,亦可混合使用2種 以上’或將2種以上共聚合。該等聚合物可藉由利用脫水 或脫胺等之聚縮合、或自由基聚合、陰離子聚合、陽離子 聚合等鏈聚合、配位聚合或開環聚合等而容易地獲得。 配向性聚合物可溶解於溶劑中而塗佈。作為溶劑,可列 舉:水;甲醇、乙醇、乙二醇、異丙醇、丙二醇、甲基溶 纖劑、丁基溶纖劑、丙二醇單甲基醚等醇溶劑;乙酸乙 酉曰乙SiL 丁自曰、乙一醇曱基喊乙酸醋、γ_ 丁内g旨、丙二醇 甲基醚乙酸酯、乳酸乙酯等酯溶劑;丙酮、甲基乙基酮、 %戊酮、環己酮、甲基戊基酮、甲基異丁基酮等酮溶劑; 戊烷、己烷、庚烷等脂肪族烴溶劑;曱苯、二甲苯等芳香 族烴溶劑;乙腈等腈溶劑;㈣氫呋喃、二曱氧基乙烷等醚 各劑,及氣仿、氣苯等經氣取代之烴溶劑。該等有機溶劑 可單獨使用,亦可組合使用兩種以上。 又,為了形成配向膜,亦可直接使用市售之配向膜材 料。作為市售之配向膜材料,可列舉:Sunever(註冊商 標,日產化學工業(股)製造)或〇pt〇mer(註冊商標, (股)製造)等。 若使用此種配向膜,則可降低不均,因此可提供環境耐 性或機械耐性進一步提高之光學膜。 158656.doc •22- 201224125 作為於上述支持基材上形成配向膜之方法,例如可於上 述支持基材上塗佈上述配向性聚合物之溶液或市售之配向 膜材料,其後進行退火,藉此於上述支持基材上形成配向 膜》藉由此種方式獲得之配向膜之厚度例如為1〇 nm〜10000 nm ’ 較佳為 1〇 nm〜10〇〇 nm。 為了對上述配向膜賦予配向限制力,較佳為視需要進行 摩擦或偏光UV照射。可藉由賦予配向限制力而使聚合性 液晶化合物配向至所期望之方向。 作為摩擦配向膜之方法,例如可列舉將纏繞摩擦布並旋 轉之摩擦輥與放置於載物台上進行搬送之配向膜接觸之方 法。於進行摩擦或偏光UV照射時,若進行遮蔽,則亦可 於所得之偏光元件上形㈣相軸之方向不同之複數個區域 (圖案)。 關於在基板上塗佈聚合性液晶組合物而獲得之塗佈膜, 就成膜性方面而言’較佳為將塗佈膜中所含之溶劑等揮發 性成分乾燥。作為乾燥方法,可列舉:自然乾燥法、通風 乾燥法及減壓乾燥法。作為乾燥溫度,較佳為0〜250。(:, 更佳為50〜220 C。作為乾燥時間,較佳為1〇秒〜6〇分鐘, 更佳為30秒〜30分鐘。 為了藉由上述塗佈膜由&amp;人〜人,, 、中所3之聚合性液晶組合物之成分 而形成液晶相’將塗係腔由入 _ 忡瞑中所含之聚合性液晶化合物加熱201224125 Step of coating film (2): Step (3) of forming a liquid crystal phase in the coating film obtained in the step (1): a film having a liquid crystal phase formed by the step (2) The step of obtaining a polymer film by polymerizing a polymerizable liquid crystal compound contained in the film as a method of coating the substrate is exemplified by an extrusion coating method, a direct gravure coating method, a reverse gravure coating method, a CAP coating method, Mold coating method, $.* /3⁄4 coating method, bar coating method and spin coating method. Examples of the substrate include glass, a plastic sheet, a plastic film, and a light-transmitting film. Examples of the light transmissive film include polyolefin films such as polyethylene, polypropylene, and norbornene thin polymer, polyvinyl alcohol film, polyethylene terephthalate film, polymethacrylate film, and polyacrylic acid. An ester film, a cellulose ester film, a polyethylene dicarboxylate film, a polycarbonate film, a polyfluorene film, a polyether sulfone film, a polyether ketone film, a polyphenylene sulfide film, and a polyphenylene ether film. By using the substrate, it is possible to easily operate without causing damage or the like when manufacturing, transporting, or storing the optical film. In the method for producing an optical film of the present invention, it is preferred that an alignment film is formed on the substrate. In this case, the polymerizable liquid crystal composition of the present invention is coated on the alignment film. The alignment film preferably has solvent resistance which is not dissolved by coating or the like of the polymerizable liquid crystal composition of the present invention. Further, it is preferable to have the heat-preserving property in the heat treatment for removing the solvent or the alignment of the liquid crystal. Further, it is preferable that the alignment film which does not cause peeling or the like due to friction or the like. The alignment film preferably contains an alignment polymer or a composition containing an alignment polymer. As the above-mentioned alignment polymer, .J J enumerates. 1.58656.doc •21-201224125 polyamine or gelatin having a guanidine bond in the molecule, and hydrolysis thereof as a ruthenium imine bond in the molecule Polylysine, polyvinyl alcohol, alkyl modified polyvinyl alcohol, polyacrylamide, polycarbazole, polyethyleneimine, polystyrene, polyvinylpyrrolidone, polyacrylic acid, poly Polymers such as acrylates. Among them, polyvinyl alcohol is preferred. These polymers may be used singly or in combination of two or more kinds or two or more kinds thereof. These polymers can be easily obtained by polycondensation using dehydration or deamination, or chain polymerization such as radical polymerization, anionic polymerization or cationic polymerization, coordination polymerization or ring-opening polymerization. The alignment polymer can be coated by dissolving in a solvent. Examples of the solvent include water; alcohol solvents such as methanol, ethanol, ethylene glycol, isopropanol, propylene glycol, methyl cellosolve, butyl cellosolve, and propylene glycol monomethyl ether; and ethyl acetate, SiL, and Ethyl alcohol ketone is called acetate vinegar, γ_ butyl ke, propylene glycol methyl ether acetate, ethyl lactate and other ester solvents; acetone, methyl ethyl ketone, % pentanone, cyclohexanone, methyl amyl ketone a ketone solvent such as methyl isobutyl ketone; an aliphatic hydrocarbon solvent such as pentane, hexane or heptane; an aromatic hydrocarbon solvent such as toluene or xylene; a nitrile solvent such as acetonitrile; and (iv) hydrogen furan and dimethoxy group Each of the ethers such as an alkane, and a hydrocarbon solvent such as a gas-like or gas-benzene-substituted gas. These organic solvents may be used singly or in combination of two or more. Further, in order to form an alignment film, a commercially available alignment film material can be used as it is. The commercially available alignment film material may, for example, be Sunever (registered trademark, manufactured by Nissan Chemical Industries Co., Ltd.) or 〇pt〇mer (registered trademark, manufactured by the company). When such an alignment film is used, unevenness can be reduced, and thus an optical film having further improved environmental resistance or mechanical resistance can be provided. 158656.doc • 22- 201224125 As a method of forming an alignment film on the above support substrate, for example, a solution of the above-mentioned alignment polymer or a commercially available alignment film material may be applied onto the above-mentioned support substrate, followed by annealing. Thereby, the alignment film is formed on the support substrate. The thickness of the alignment film obtained in this manner is, for example, from 1 nm to 10000 nm', preferably from 1 nm to 10 nm. In order to impart an alignment regulating force to the above alignment film, it is preferred to perform rubbing or polarized UV irradiation as needed. The polymerizable liquid crystal compound can be aligned to a desired direction by imparting an alignment regulating force. As a method of rubbing the alignment film, for example, a method in which a rubbing roll wound with a rubbing cloth is rotated and brought into contact with an alignment film placed on a stage to be conveyed can be mentioned. When performing rubbing or polarized UV irradiation, if masking is performed, a plurality of regions (patterns) having different directions of the (4) phase axes may be formed on the obtained polarizing element. In the coating film obtained by coating the polymerizable liquid crystal composition on the substrate, it is preferable to dry the volatile component such as a solvent contained in the coating film in terms of film formability. Examples of the drying method include a natural drying method, a ventilation drying method, and a reduced pressure drying method. The drying temperature is preferably 0 to 250. (:, more preferably 50 to 220 C. As the drying time, it is preferably 1 second to 6 minutes, more preferably 30 seconds to 30 minutes. To be coated by the above film &amp; And forming a liquid crystal phase by the components of the polymerizable liquid crystal composition of the third embodiment, and heating the coating system cavity by the polymerizable liquid crystal compound contained in the _ 忡瞑

至顯不液晶相之溫度即·jp。外、六gI p 了 §亥液晶相較佳為層列相。又, 更佳為將塗佈膜中所含$ # 之聚口性液晶化合物加熱至轉移至 向列相之溫度以上,繼而收# Μ人 繼而將该聚合性液晶化合物冷卻至顯 158656.doc •23· 201224125 示層列相之溫度,藉此獲得形成有層列相之膜β 於聚合性液晶組合物含有2種以上之聚合性&amp;晶化合物 之情形時’藉由對以聚合性液晶組合物中所含之含量比調 整該聚合性液晶化合物而成之混合物測定顯示液晶相之溫 度,可決定藉由重合性液晶組合物之成分而形成液晶相之 溫度。 藉由經由向列相,聚合性液晶組合物中所含之調平劑變 得容易流動’可容易地獲得水平配向之膜。作為加熱之溫 度,較佳為肖列相轉移點以上且較向列相轉移點高1〇〇度 之溫度以下,更佳為向列相轉移點以上且較向列相轉移點 高5〇度之溫度以下。亦可同時進行用以使液晶相配向之加 熱與上述乾燥。 其次,可藉由使形成液晶相之膜中所含之聚合性液晶化 合物聚合而獲得光學膜。藉由進行聚合,而成為具有耐久 之光予膜。使其聚合之方法只要根據聚合性液晶化合物 所具有之聚合性基之種類進行選擇即可。若該聚合性基為 光聚合性基,則可藉由光聚合法進行聚合,若為熱聚合性 基,可藉由熱聚合法進行聚合,於本發明之光學膜之製造 方法中’較佳為光聚合法。若為光聚合法,則未必需要加 熱至高溫’因此可使用冑熱性較低之基板。%聚合法係藉 由對形成有液晶相之膜照射可見光、紫外光或雷射光而進 行。就容易操作方面而言,較佳為紫外光。光照射係於使 膜^成液晶相之狀態下進行。亦可如上所述於顯示液晶相 之μ度下進行光照射❶此時,亦可藉由進行遮蔽或顯影等 158656.doc -24- 201224125 而對光學膜進行圖案化。 於使膜中所含之聚合性液晶化合物聚合後, 剝離形成於基板上之光學膜。又’除剝離基板之步ς之 .外’亦可進而包括剝離配向膜之步驟。藉此,可獲得單層 之本發明之光學膜》本發明之光學膜之膜厚較佳為〇3〜2〇 μιη,更佳為0.5〜1〇 ,更佳* 〇 ς c μπι更佳為〇.5〜5 μϊη。若膜厚為上述 範圍内,則可容易地獲得水平配向為層列相上之光學膜。 於本發明之光學膜含有二色性色素之情形時,作為二色 比優異之偏光膜有用。又’於不含二色性色素之情形時, 作為對比度優異之相位差膜有用。 本發明之顯示裝置含有本發明之光學膜。所謂顯示裝 置,係指具有顯示元件之裝置,其含有發光元件或發光裝 置作為發光源。作為顯示裝置,可列舉:液晶顯示裝置、 有機電致發光(EL,Electro Luminescence)顯示裝置、無機 電致發光(EL)顯示裝置、電子發射顯示裝置(例如場發射 顯示裝置(FED ’ Field Emission Display)、表面電場發射 顯示裝置(SED,Surface Electron Emitter Display))、電子 紙(使用電子墨水或電泳元件之顯示裝置、電漿顯示裝 置、投射型顯示裝置(例如柵狀光閥(GLV,Grating LightTo the temperature of the liquid crystal phase, ie jp. Outside, six gI p § hai liquid phase is preferably a smectic phase. Further, it is more preferable to heat the polycyclic liquid crystal compound contained in the coating film to a temperature higher than the temperature of the nematic phase, and then to cool the polymerizable liquid crystal compound to 158656.doc. 23·201224125 The temperature of the phase of the layer is obtained, whereby the film β having the smectic phase is formed, and when the polymerizable liquid crystal composition contains two or more kinds of polymerizable &amp; crystalline compounds, The content of the liquid crystal phase is determined by measuring the mixture of the polymerizable liquid crystal compound, and the temperature of the liquid crystal phase is determined by the composition of the superposed liquid crystal composition. By the nematic agent, the leveling agent contained in the polymerizable liquid crystal composition becomes easy to flow, and the film of the horizontal alignment can be easily obtained. The heating temperature is preferably not less than the zeolitic phase transition point and not more than 1 degree higher than the nematic phase transition point, more preferably more than the nematic phase transition point and 5 degrees higher than the nematic phase transition point. Below the temperature. Heating for the alignment of the liquid crystals and drying as described above may also be carried out simultaneously. Next, an optical film can be obtained by polymerizing a polymerizable liquid crystal compound contained in a film forming a liquid crystal phase. By carrying out polymerization, a film having a durable light is obtained. The method of polymerizing it may be selected according to the type of the polymerizable group which the polymerizable liquid crystal compound has. When the polymerizable group is a photopolymerizable group, it can be polymerized by a photopolymerization method, and if it is a thermally polymerizable group, it can be polymerized by a thermal polymerization method, and is preferably used in the method for producing an optical film of the present invention. For photopolymerization. In the case of the photopolymerization method, it is not necessary to heat to a high temperature. Therefore, a substrate having a low heat resistance can be used. The % polymerization method is carried out by irradiating a film having a liquid crystal phase with visible light, ultraviolet light or laser light. In terms of ease of handling, ultraviolet light is preferred. The light irradiation is performed in a state where the film is formed into a liquid crystal phase. Alternatively, light irradiation may be performed at a degree of display liquid crystal phase as described above. At this time, the optical film may be patterned by masking or developing 158656.doc -24 - 201224125. After the polymerizable liquid crystal compound contained in the film is polymerized, the optical film formed on the substrate is peeled off. Further, the step of stripping the substrate may further include the step of peeling off the alignment film. Thereby, a single layer of the optical film of the present invention can be obtained. The film thickness of the optical film of the present invention is preferably 〇3 to 2 〇μηη, more preferably 0.5 to 1 〇, more preferably 〇ς c μπι is more preferably 〇.5~5 μϊη. When the film thickness is within the above range, an optical film which is horizontally aligned in the smectic phase can be easily obtained. When the optical film of the present invention contains a dichroic dye, it is useful as a polarizing film excellent in dichroic ratio. Further, in the case where the dichroic dye is not contained, it is useful as a retardation film excellent in contrast. The display device of the present invention contains the optical film of the present invention. The term "display device" refers to a device having a display element that contains a light-emitting element or a light-emitting device as a light-emitting source. Examples of the display device include a liquid crystal display device, an organic electroluminescence (EL) display device, an inorganic electroluminescence (EL) display device, and an electron emission display device (for example, a field emission display device (FED 'Field Emission Display) ), surface electric field emission display device (SED), electronic paper (display device using electronic ink or electrophoretic element, plasma display device, projection display device (eg, grating light valve (GLV, Grating Light)

Valve)顯示裝置、具有數位微鏡裝置(DMD,Digital Micro-mirror Device)之顯示裝置)及壓電陶瓷顯示器。作 為液晶顯示裝置,可列舉:透射塑液晶顯示裝置、半透射 型液晶顯示裝置、反射型液晶顯示裝置、直視形液晶顯示 裝置及投影型液晶顯示裝置。上述顯示裝置可為顯示二維 158656.doc •25· 201224125 影像之顯示裝置,亦可為顯示三維影像之立體顯示裝置。 圖1係表示作為本發明之顯示裝置之一的液晶顯示裝置 10之概略圖。由兩片基板14a及基板14b夾持液晶層17。 於基板14a之液晶層π側配置有彩色濾光片15。彩色渡 光片15夾持液晶層17並配置於與像素電極22對向之位置, 黑矩陣20配置於與像素電極間之邊界對向之位置。透明電 極16覆蓋該等。亦可於彩色濾光片15與透明電極16之間具 有保護層。 於基板14b之液晶層π側規則地配置有薄膜電晶體21與 像素電極22 ^像素電極22夾持液晶層17並配置於與彩色濾 光片1 5對向之位置。於薄膜電晶體21與像素電極22之間配 置有具有連接孔(未圖示)之層間絕緣膜18。 作為基板14a及基板14b,可列舉玻璃基板及塑膠基板。 於製造形成於該荨基板上之彩色濾光片15或薄膜電晶體21 時’於需加熱至高溫之情形時,基板14a及基板1仆較佳為 玻璃基板。 作為薄膜電晶體21 ’可列舉形成於石英基板上之高溫聚 石夕電晶體、形成於玻璃基板上之低溫聚矽電晶體、及形成 於玻璃基板或塑膠基板上之非晶矽電晶體。為了實現液晶 顯示裝置之小型化,亦可將驅動IC(Integrated Circuit,積 體電路)形成於基板14b上。 於透明電極16與像素電極22之間配置有液晶層17。為了 將基板14a與基板14b之間的距離保持固定,而於液晶層17 中形成有間隔物23。亦可在形成於基板! 4a及基板14b上之 158656.doc -26- 201224125 層之與液晶層17接觸之面上,分別配置用以使液晶層17中 所含之液晶化合物配向至所需方向的配向膜。 各部件係以基板14a、彩色濾光片15及黑矩陣20、透明 電極16、液晶層17、像素電極22、層間絕緣膜18及薄膜電 晶體21、以及基板^匕之順序進行積層。 於夾持此種液晶層17之基板14a及基板14b之外側積層有 各種光學膜、例如偏光膜(例如直線偏光元件)或相位差膜 (例如1/4波長板、光學補償膜)。於圖1中,於基板14a之外 側依序積層有相位差膜13a、偏光膜12a,於基板i4b之外 側依序積層有相位差膜13b、偏光膜12b。選自由偏光膜 12a、偏光膜12b、相位差膜na及相位差膜13b所組成之群 中之至少1種為本發明之光學膜。藉由配置本發明之光學 膜’可賦予將入射光轉換成直線偏光或圓偏光之功能或光 學性補償由液晶引起之相位之偏移的功能。再者,亦可根 據液晶顯示裝置之結構或液晶層丨7中所含之液晶化合物之 種類’而不配置相位差膜133及13b。於偏光膜i2a之外側 配置有用以防止外光之反射之抗反射膜11β根據本發明之 光學媒’可實現顯示裝置之薄型化。 作為選自由偏光膜12a及12b、以及該相位差膜13a及13b 所組成之群中之至少i種,亦可使用將本發明之光學膜、 配向膜及製造上述光學膜時所使用之基板積層而成之積層 體。 於偏光膜12b之外側配置有作為發光源之背光單元丨9。 背光單元19含有光源、導光體、反射板、擴散片及視角調 158656.doc • 27· 201224125 整片。作為光源,可使用電致發光(el)、冷陰極管、熱陰 極管、發光二極體(LED,Light-Emitting Diode)、雷射光 源、水銀燈等各種光源。只要結合光源之特性選擇本發明 之光學膜即可。 於液晶顯示裝置10為透射型液晶顯示裝置之情形時,自 背光單元19中之光源發出之白色光入射至導光體中,藉由 反射板而改變光路並被擴散片擴散。擴散光係藉由視角調 整片以具有所需指向性之方式進行調整後,自背光單元19 入射至偏光膜12b。 無偏光之入射光中’僅某一直線偏光透射液晶面板之偏 光膜12b。§亥直線偏光藉由相位差膜i3b而轉換為圓偏光, 依序透射基板14b、像素電極22等而到達液晶層17。 根據像素電極22與對向之透明電極16之間之電位差之有 無’液晶層17中所含之液晶化合物之配向狀態發生變化, 並抑制自液晶顯示裝置1 〇出射之光之亮度。於液晶層丨7為 使利用相位差膜13b所轉換之圓偏光直接透射之配向狀態 之情形時,若該圓偏光透射液晶層17、透明電極16,某特 定之波長範圍之光透射彩色濾光片15而到達相位差膜 i3a’進而透射偏光膜! 2a及抗反射膜丨丨,則該像素最明亮 地顯示由彩色濾光片決定之顏色。反之,於液晶層17為使 利用相位差膜13b所轉換之圓偏光轉換並透射之配向狀態 之情形時,於透射液晶層丨7、透明電極丨6及彩色濾光片i 5 之光幾乎完全被相位差膜13a與偏光元件12a吸收之情形 時’該像素顯示黑色。若液晶層17為該等2種狀態之中間 158656.doc -28- 201224125 配向狀態 則自液晶顯示裝置丨0出射 述兩者之中間 因此該像素顯示中間 之光之亮度亦成為上 色。 於液晶顯示裳置10為半透射型液晶顯示裝置之情形時, 像素電極22具有由透明之材料形成之透射部與由使光反射 之材料形成的反射部,於透射部中,以與上述透射型液晶 顯丁裝置相同之方式顯示影像。另__方面,於反射部中, 外光自抗反射膜U之方向入射至液晶顯示裝置,透射偏光 膜12&amp;與相位差膜13a之圓偏光通過液晶層17,㈣像素電 極22反射而用於顯示。 圖2係表示作為本發明之顯示裝置之一的將本發明之光 學膜配置於基板之内部(液晶17側)之液晶顯示裝置24之概 略圖°於液晶顯示裝置24中,各部件係以抗反射、基 板14a、偏光膜12a、相位差膜Ua、彩色濾光片15及黑矩 陣20、透明電極16、液晶層17、像素電極22、層間絕緣膜 18及薄膜電晶體21、相位差膜13b、偏光膜12b、基板 14b、背光單兀19之順序進行積層。選自由偏光膜12a、偏 光膜12b、相位差膜na及相位差膜13b所組成之群中之至 少1種為本發明之光學膜。亦可使用將本發明之光學膜、 配向膜及製造上述光學膜時所使用之基板積層而成之積層 體。藉由配置本發明之光學膜’可對液晶顯示裝置24賦予 使入射光成為直線偏光或圓偏光之功能或光學性補償由液 晶所引起之相位之偏移的功能。再者,亦可根據液晶顯示 裝置之結構或液晶層17中所含之液晶化合物之種類,而不 配置相位差膜13a及13b。 158656.doc 29· 201224125 圖3係表示作為本發明之顯示裝置之一的示裝置 之概略圖。EL顯示裝置30係於形成有像素電極35之基板33 上積層有作為發光源之有機功能層36及陰極電極37者。夾 持基板3 3並於與有機功能層3 6相反之側配置有相位差膜3 2 及偏光膜31。選自由相位差膜32及偏光膜31所組成之群中 之至少1種為本發明之光學膜。對像素電極35施加正電 壓,對陰極電極37施加負電壓,對像素電極35及陰極電極 37間施加直流電流,藉此有機功能層刊發光。作為發光源 之有機功能層36包括電子傳輸層、發光層、電洞傳輸層 等。自有機功能層36出射之光通過像素電極35、層間絕緣 膜34、基板33、相位差膜32及偏光該。代替有機功能層 36而具有無機功能層之無機EL顯示裝置亦為本發明之顯示 裝置之一。 為了製造EL顯示裝置30,首先於基板33上將薄膜電晶體 40形成為所需形狀。並且,形成層間絕緣膜,繼而利用 滅鑛法形成像素電極35,進行圖案化。其後,積層有機功 能層3 6 » 作為基板33 ’可列舉:藍寶石玻璃基板、石英玻璃基 板、納玻璃基板、氧化铭等陶曼基板、銅等金屬基板、塑 膠基板等。亦可於基板上形成導熱性膜。作為導熱性膜, 可列舉鑽石薄膜(DLC(Diamond_Uke Carb〇n,類鑽碳) 等)。於將像素電極35設為反射型之情形時,光向與基板 33相反之方向出射。因此’不僅可使用透明材料亦可使 用不鏽鋼等非透射材料。基板可由單一材料形成,又,亦 158656.doc 30· 201224125 可為利用接著劑貼合複數片基板而成之積層基板。該等基 板可為板狀,亦可為膜狀。 作為薄膜電晶體4〇,使用通常之多晶石夕電晶體即可。薄 膜電晶體40係設置於像素電極35之端部,其大小為1〇〜3〇 μιη左右。再者,像素電極35之面積為2〇 μιηχ2〇 μιη〜3〇〇 μιηχ300 μηι左右。 基板33上設置有薄膜電晶體4〇之配線電極。關於配線電 極,其電阻較低,且具有與像素電極35電性連接而將電阻 值抑制為較低之功能,通常該配線電極係使用含有入卜A1 及過渡金屬(其中Ti除外)、鈦或氮化鈦(TiN)中之任j種或2 種以上者。 於薄膜電晶體40與像素電極35之間設置有層間絕緣膜 34。層間絕緣膜34只要為利用濺鍍或真空蒸鍍將以〇2等氧 化矽、氮化矽等無機系材料成膜而成者,由s〇G(旋塗玻 璃,SPin-on-glass)形成之氧化矽層、光阻抗蝕劑、聚醯亞 胺、丙烯酸系樹脂等樹脂系材料之塗膜等具有絕緣性者, 則可為任意者。 於層間絕緣膜34上形成阻隔壁41。阻隔壁41係配置於像 素電極35之周邊部(鄰接像素間)。作為阻隔壁“之材料, 可列舉.丙烯酸系樹脂、聚醯亞胺樹脂等。阻隔壁4丨之厚 度較佳為1.0 μη!以上且3.5 μΐΏ以下,更佳為15 μιη以上且 2.5 μηι以下。 其次,對包括作為透明電極之像素電極35、作為發光源 之有機功能層36、及陰極電極37iEL元件進行說明。有機 158656.doc -31- 201224125 功能層36係分別具有至少1層之電洞傳輸層及發光層,例 如依序具有電子注入傳輸層、發光層、電洞傳輸層、電洞 注入層。 作為像素電極35,可列舉ITO(摻錫氧化銦)、IZ〇(摻鋅 氧化銦)、IGZO、ZnO、Sn02及 Ιη203,尤佳為 ITO及 IZO。 像素電極3 5之厚度只要具有可充分地進行電洞注入之固定 厚度以上之厚度即可’較佳為設為10〜500 nm左右。 像素電極35可藉由蒸鍍法而形成,較佳為藉由濺鍍法而 形成。作為濺鍍氣體’並無特別限制,使用Ar、He、 Ne ' Kr、Xe等惰性氣體或該等之混合氣體即可。 作為陰極電極37之構成材料,例如較佳為使用K、u、A display device, a display device having a digital micro-mirror device (DMD), and a piezoelectric ceramic display. Examples of the liquid crystal display device include a transmissive liquid crystal display device, a transflective liquid crystal display device, a reflective liquid crystal display device, a direct-view liquid crystal display device, and a projection type liquid crystal display device. The display device may be a display device for displaying two-dimensional 158656.doc •25·201224125 images, or a stereoscopic display device for displaying three-dimensional images. Fig. 1 is a schematic view showing a liquid crystal display device 10 which is one of the display devices of the present invention. The liquid crystal layer 17 is sandwiched between the two substrates 14a and 14b. A color filter 15 is disposed on the liquid crystal layer π side of the substrate 14a. The color filter 15 sandwiches the liquid crystal layer 17 and is disposed at a position opposed to the pixel electrode 22, and the black matrix 20 is disposed at a position facing the boundary between the pixel electrodes. The transparent electrode 16 covers these. A protective layer may also be provided between the color filter 15 and the transparent electrode 16. The thin film transistor 21 and the pixel electrode 22 are disposed regularly on the liquid crystal layer π side of the substrate 14b. The pixel electrode 22 sandwiches the liquid crystal layer 17 and is disposed at a position facing the color filter 15. An interlayer insulating film 18 having a connection hole (not shown) is disposed between the thin film transistor 21 and the pixel electrode 22. Examples of the substrate 14a and the substrate 14b include a glass substrate and a plastic substrate. When the color filter 15 or the thin film transistor 21 formed on the substrate is manufactured, when the substrate is heated to a high temperature, the substrate 14a and the substrate 1 are preferably glass substrates. Examples of the thin film transistor 21' include a high-temperature polycrystalline silicon crystal formed on a quartz substrate, a low-temperature polycrystalline silicon crystal formed on a glass substrate, and an amorphous germanium transistor formed on a glass substrate or a plastic substrate. In order to reduce the size of the liquid crystal display device, a driver IC (integrated circuit) may be formed on the substrate 14b. A liquid crystal layer 17 is disposed between the transparent electrode 16 and the pixel electrode 22. In order to keep the distance between the substrate 14a and the substrate 14b fixed, a spacer 23 is formed in the liquid crystal layer 17. Can also be formed on the substrate! On the surface of the layer 158656.doc -26-201224125 on the substrate 14b which is in contact with the liquid crystal layer 17, an alignment film for aligning the liquid crystal compound contained in the liquid crystal layer 17 to a desired direction is disposed. Each member is laminated in the order of the substrate 14a, the color filter 15, the black matrix 20, the transparent electrode 16, the liquid crystal layer 17, the pixel electrode 22, the interlayer insulating film 18, the thin film transistor 21, and the substrate. Various optical films such as a polarizing film (for example, a linear polarizing element) or a retardation film (for example, a quarter-wave plate or an optical compensation film) are laminated on the outer side of the substrate 14a and the substrate 14b sandwiching the liquid crystal layer 17. In Fig. 1, a retardation film 13a and a polarizing film 12a are sequentially laminated on the outer side of the substrate 14a, and a retardation film 13b and a polarizing film 12b are sequentially laminated on the outer side of the substrate i4b. At least one selected from the group consisting of the polarizing film 12a, the polarizing film 12b, the retardation film na, and the retardation film 13b is the optical film of the present invention. By arranging the optical film 'of the present invention', it is possible to impart a function of converting incident light into linearly polarized or circularly polarized light or optically compensating for a phase shift caused by liquid crystal. Further, the retardation films 133 and 13b may not be disposed depending on the configuration of the liquid crystal display device or the type of the liquid crystal compound contained in the liquid crystal layer 丨7. The anti-reflection film 11β for preventing reflection of external light is disposed on the outer side of the polarizing film i2a to reduce the thickness of the display device according to the optical medium of the present invention. As the at least one selected from the group consisting of the polarizing films 12a and 12b and the retardation films 13a and 13b, the optical film, the alignment film, and the substrate used in the production of the optical film may be laminated. A layered body. A backlight unit 作为9 as a light source is disposed on the outer side of the polarizing film 12b. The backlight unit 19 includes a light source, a light guide, a reflector, a diffusion sheet, and a viewing angle adjustment. 158656.doc • 27· 201224125 The entire film. As the light source, various light sources such as electroluminescence (el), cold cathode tube, hot cathode tube, LED (Light-Emitting Diode), laser light source, and mercury lamp can be used. The optical film of the present invention may be selected in combination with the characteristics of the light source. When the liquid crystal display device 10 is a transmissive liquid crystal display device, white light emitted from a light source in the backlight unit 19 is incident on the light guide body, and the optical path is changed by the reflector to be diffused by the diffusion sheet. The diffused light is incident from the backlight unit 19 to the polarizing film 12b by adjusting the viewing angle adjustment sheet so as to have desired directivity. In the incident light of the non-polarized light, only a certain linearly polarized light is transmitted through the polarizing film 12b of the liquid crystal panel. The linear polarized light is converted into circularly polarized light by the retardation film i3b, and sequentially passes through the substrate 14b, the pixel electrode 22, and the like to reach the liquid crystal layer 17. The alignment state of the liquid crystal compound contained in the liquid crystal layer 17 changes depending on the presence or absence of the potential difference between the pixel electrode 22 and the opposite transparent electrode 16, and the brightness of the light emitted from the liquid crystal display device 1 is suppressed. In the case where the liquid crystal layer 丨7 is in an alignment state in which the circularly polarized light converted by the retardation film 13b is directly transmitted, if the circularly polarized light transmits the liquid crystal layer 17 and the transparent electrode 16, the light of a specific wavelength range is transmitted through the color filter. The sheet 15 reaches the retardation film i3a' and further transmits the polarizing film! 2a and the anti-reflection film 丨丨, the pixel displays the color determined by the color filter most brightly. On the other hand, when the liquid crystal layer 17 is in an alignment state in which the circularly polarized light converted by the retardation film 13b is converted and transmitted, the light transmitted through the liquid crystal layer 丨7, the transparent electrode 丨6, and the color filter i5 is almost completely When the retardation film 13a and the polarizing element 12a are absorbed, the pixel displays black. If the liquid crystal layer 17 is in the middle of the two states 158656.doc -28-201224125, the liquid crystal display device 丨0 emits the middle of the two, so that the brightness of the light in the middle of the pixel is also the upper color. In the case where the liquid crystal display panel 10 is a semi-transmissive liquid crystal display device, the pixel electrode 22 has a transmissive portion formed of a transparent material and a reflecting portion formed of a material that reflects light, in the transmissive portion, and the above-described transmissive portion. The type of liquid crystal display device displays images in the same manner. Further, in the reflection portion, external light is incident on the liquid crystal display device from the direction of the anti-reflection film U, and the circularly polarized light of the transmission polarization film 12&amp; and the retardation film 13a passes through the liquid crystal layer 17, and (4) the pixel electrode 22 is used for reflection. For display. 2 is a schematic view showing a liquid crystal display device 24 in which an optical film of the present invention is disposed inside a substrate (on the liquid crystal 17 side) as one of display devices of the present invention. In the liquid crystal display device 24, each component is resistant. Reflection, substrate 14a, polarizing film 12a, retardation film Ua, color filter 15 and black matrix 20, transparent electrode 16, liquid crystal layer 17, pixel electrode 22, interlayer insulating film 18, thin film transistor 21, retardation film 13b The polarizing film 12b, the substrate 14b, and the backlight unit 19 are laminated in this order. At least one of the group consisting of the free polarizing film 12a, the polarizing film 12b, the retardation film na, and the retardation film 13b is an optical film of the present invention. A laminate obtained by laminating the optical film, the alignment film, and the substrate used in the production of the optical film of the present invention can also be used. By arranging the optical film of the present invention, the liquid crystal display device 24 can be provided with a function of making the incident light linearly polarized or circularly polarized or optically compensating for the phase shift caused by the liquid crystal. Further, the retardation films 13a and 13b may not be disposed depending on the structure of the liquid crystal display device or the type of the liquid crystal compound contained in the liquid crystal layer 17. 158656.doc 29· 201224125 Fig. 3 is a schematic view showing an apparatus as one of display devices of the present invention. The EL display device 30 is formed by laminating an organic functional layer 36 and a cathode electrode 37 as light-emitting sources on a substrate 33 on which the pixel electrodes 35 are formed. The retardation film 3 2 and the polarizing film 31 are disposed on the side opposite to the organic functional layer 36 while sandwiching the substrate 33. At least one selected from the group consisting of the retardation film 32 and the polarizing film 31 is the optical film of the present invention. A positive voltage is applied to the pixel electrode 35, a negative voltage is applied to the cathode electrode 37, and a direct current is applied between the pixel electrode 35 and the cathode electrode 37, whereby the organic functional layer emits light. The organic functional layer 36 as a light-emitting source includes an electron transport layer, a light-emitting layer, a hole transport layer, and the like. The light emitted from the organic functional layer 36 passes through the pixel electrode 35, the interlayer insulating film 34, the substrate 33, the retardation film 32, and the polarized light. An inorganic EL display device having an inorganic functional layer instead of the organic functional layer 36 is also one of the display devices of the present invention. In order to manufacture the EL display device 30, the thin film transistor 40 is first formed on the substrate 33 in a desired shape. Further, an interlayer insulating film is formed, and then the pixel electrode 35 is formed by a metallurgical method to perform patterning. Then, the laminated organic functional layer 3 6 » can be exemplified by a sapphire glass substrate, a quartz glass substrate, a nano glass substrate, a Tauman substrate such as Oxide, a metal substrate such as copper, or a plastic substrate. A thermally conductive film can also be formed on the substrate. As the thermal conductive film, a diamond thin film (DLC (Diamond_Uke Carb〇n, diamond-like carbon) or the like) can be cited. When the pixel electrode 35 is of a reflective type, light is emitted in a direction opposite to the substrate 33. Therefore, it is possible to use not only a transparent material but also a non-transmissive material such as stainless steel. The substrate may be formed of a single material, and may also be a laminated substrate obtained by laminating a plurality of substrates with an adhesive, in addition to 158656.doc 30·201224125. The substrates may be in the form of a plate or a film. As the thin film transistor 4, a usual polycrystalline crystal can be used. The thin film transistor 40 is disposed at the end of the pixel electrode 35 and has a size of about 1 〇 to 3 〇 μιη. Furthermore, the area of the pixel electrode 35 is about 2 〇 μηηχ2〇 μιη~3〇〇 μιηχ300 μηι. A wiring electrode of a thin film transistor 4 is provided on the substrate 33. The wiring electrode has a low electric resistance and has a function of electrically connecting to the pixel electrode 35 to suppress the resistance value to a low level. Generally, the wiring electrode is used to contain the inclusion A1 and the transition metal (excluding Ti), titanium or Any one or two or more of titanium nitride (TiN). An interlayer insulating film 34 is provided between the thin film transistor 40 and the pixel electrode 35. The interlayer insulating film 34 is formed of an inorganic material such as yttrium oxide or tantalum nitride such as ruthenium 2 by sputtering or vacuum deposition, and is formed of s〇G (spin-coated glass, SPin-on-glass). Any one of the coating film of a resin material such as a ruthenium oxide layer, a photoresist, a polyimide, or an acrylic resin may have any insulating property. A barrier wall 41 is formed on the interlayer insulating film 34. The barrier 41 is disposed on the peripheral portion of the pixel electrode 35 (between adjacent pixels). Examples of the material of the barrier ribs include an acrylic resin, a polyimide resin, etc. The thickness of the barrier rib 4 较佳 is preferably 1.0 μη! or more and 3.5 μΐΏ or less, more preferably 15 μm or more and 2.5 μηη or less. Next, the pixel electrode 35 as a transparent electrode, the organic functional layer 36 as a light source, and the cathode electrode 37iEL element will be described. Organic 158656.doc -31- 201224125 The functional layer 36 has at least one layer of hole transmission. The layer and the light-emitting layer have, for example, an electron injecting and transporting layer, a light emitting layer, a hole transporting layer, and a hole injecting layer. Examples of the pixel electrode 35 include ITO (tin-doped indium oxide) and IZ〇 (zinc-doped indium oxide). IGZO, ZnO, Sn02, and 203203 are particularly preferably ITO and IZO. The thickness of the pixel electrode 35 can be set to about 10 to 500 nm as long as it has a thickness sufficient to sufficiently fill the hole. The pixel electrode 35 can be formed by a vapor deposition method, and is preferably formed by a sputtering method. The sputtering gas is not particularly limited, and an inert gas such as Ar, He, Ne'Kr or Xe or the like is used. Mixed Gas can. As the material constituting the cathode electrode 37 of, for example, is preferably used K, u,

Na、Mg、La、Ce、Ca、Sr、Ba、A1、Ag、In、Sn、Zn、Na, Mg, La, Ce, Ca, Sr, Ba, A1, Ag, In, Sn, Zn,

Zr等金屬%素單質、或為了提高穩定性而使用含有該等2 種成刀、3種成分之合金系。作為合金系,例如較佳為 Ag Mg(Ag . 1 〜2〇 原子 %)、A1.Li(Li : 〇 3〜14 原子。/。)、In order to improve the stability, an alloy system containing these two kinds of knives and three kinds of components is used for the purpose of improving the stability of the metal such as Zr. As the alloy system, for example, Ag Mg (Ag. 1 to 2 原子 atom%), A1. Li (Li: 〇 3 to 14 atoms//),

In Mg(Mg ’ 50〜80原子。/。)、Al.Ca(Ca : 5〜20原子。/0)等 β 陰極電極37係藉由蒸鍍法、濺鍍法等而形成。陰極電極 37之厚度較佳為0.1 nm以上,較佳為工nm〜5〇〇 nm。 電洞注入層具有使自像素電極35之電洞注入變得容易之 功能,電洞傳輸層具有傳輸電洞之功能及阻礙電子之功 月巨’亦稱為電荷注入層、電荷傳輸層。 發光層之厚度、電洞注入層與電洞傳輸層之合計厚度及 電子注入傳輸層之厚度並無特別限定,根據該等之形成方 法而有所不同,較佳為設為5 nm〜1 〇〇 nm。電洞注入層、 158656.doc •32· 201224125 電洞傳輸層令可使用各種有機化合物。對於電洞注入傳輸 層、發光層及電子注入傳輸層之形成,較佳為使用真空蒸 鑛法,其原因在於可形成均質之薄膜。 作為發光源之有機功能層3 6可使用:利用源自單重態激 子之發光(螢光)者、利用源自3重態激子之發光(磷光)者、 含有利用源自單重態激子之發光(螢光)者與利用源自3重態 激子之發光(磷光)者的有機功能層、由有機物所形成者、 由無機物所形成者、含有由有機物所形成者與由無機物所 形成者的有機功能層、高分子之材料、低分子之材料、含 有向分子之材料與低分子之材料者等。但並不限定於此, 可使用利用各種有機功能層之£1顯示裝置作為EL元件。 於陰極電極37與密封蓋39之間的空間配置乾燥劑“。其 原因在於有機功能層36不耐受濕度。利用乾燥劑38吸收水 分而防止有機功能層36之劣化。 形成於EL顯示裝置30之光入射面或光出射面上之偏光膜 31並不限定於轉換成直線偏光之偏光膜,亦可為轉換成橢 圓偏光之偏光膜。偏光膜31可僅為本發明之光學膜,亦可 貼合本發明之光學膜以外之偏光膜或相位差膜而使用。 圖4係表示作為本發明之顯示裝置之一的£1^顯示裝置44 之概略圖。EL顯示裝置44具#使用薄膜密封膜心之密封結 構’自陣列基板之相反面亦可獲得出射光。 作為薄膜密封膜42,較佳為使用在電解電容器之膜上蒸 鍍有蒸鍍DLC(類鑽碳)的DLC膜。DLC膜係水分浸透性極 差而防濕性能高。X ’亦可將DLC膜等直接蒸鍵至陰極電 158656.doc -33· 201224125 極37之表面而形成。又,亦可積層多層樹脂薄膜與金屬薄 膜而形成薄膜密封膜42。 選自由偏光膜31及相位差膜32所組成之群中之至少一種 為本發明之光學膜。 圖5係表示作為本發明之顯示裝置之一的投射型液晶顯 示裝置之概略圖。 本發明之偏光膜142及本發明之偏光膜143例如可用於投 射型液晶顯示裝置(投影儀)。 自作為發光源之光源(例如高壓水銀燈)111出射之光束首 先通過第1透鏡陣列112、第2透鏡陣列113、偏光轉換元件 114、重疊透鏡115,藉此進行反光束剖面上之亮度之均勻 化與偏光化。 具體而言,自光源111出射之光束係被將微小之透鏡 112a形成為矩陣狀之第1透鏡陣列112分割為多條微小之光 束。第2透鏡陣列113及重疊透鏡115係以經分割之光束之 分別照射作為照明對象之3個液晶面板140R、140G、140B 之整體之方式具備,因此各液晶面板入射側表面之整個面 之照明度幾乎均勻。 偏光轉換元件114包含偏光分光鏡陣列,且配置於第2透 鏡陣列113與重疊透鏡115之間。藉此承擔將源自光源之無 規偏光預先轉換成具有特定偏光方向之偏光,而降低下述 入射侧偏光元件中之光量損失,提高晝面之亮度的作用。 經亮度均勻化及偏光化之光係經由反射鏡122,利用用 以分離成RGB之3原色之雙色鏡121、123、132而分離成紅 158656.doc .14- Λ 201224125 色通道(圖5中之」R」,實線箭頭)、綠色通道(圖5中之 「G」,點線箭頭)、藍通道(圖5中之」B」’虛線箭頭)’分 別入射至液晶面板140R、140G、140B。 於液晶面板140R、140G、140B中,分別於其入射侧配 置有本發明之偏光元件膜142,於出射側配置有本發明之 偏光元件膜143。 配置於RGB各自之光路中之偏光膜142及偏光膜143係以 各自之吸收轴正交之方式配置。配置於各光路中之各液晶 面板140R、140G、140B具有藉由影像信號而將每個像素 所控制之偏光狀態轉換成光量之功能。 本發明之光學膜係藉由選擇適合所對應之通道之二色性 色素之種類,而用作於藍通道、綠色通道、紅色通道之任 一光路中耐久性均優異之光學膜。 根據液晶面板140R、140G、14〇B之各影像資料,藉由 以每個像素不同之透射率透射人射光而製成之光學像^ 用合光稜鏡15G合成,並制投料鏡⑺而放大投影 幕180上。 本發明之光學膜亦可用作電子紙光學膜。 ::電子紙,可列舉:藉由液晶等光學異向性汰 料分子之配向而進行顯示者;藉由電泳、粒子移動、 旋轉、相變化等粒子舉動而進行顯〃子 動而進行顯示者;_ &amp;八 &quot; , 、之一端移 者,藉由分子之光吸收而進行顯示者 ^員不 合進行自發光而進行㈣^ a由電子與電洞結 仃顯不者專。作為具體之顯示方式,可 158656.doc -35- 201224125 列舉:微膠囊型電泳方式、 動型電泳方式、球狀扭綾—t '電泳方式、垂直移 4圓扣…方式、磁扭轉向列球方 ;、=t方式、帶電碳粉方式、電子粉流體方 永方式、磁感熱方式、電濁濕方式、光散射(透明/ 白濁變化)方式、膽固醇狀 光散射(透月/ 液晶方式、雙衫性㈣;^ 式、膽固醇狀 …主, 晶方式、鐵電性液晶方式、二 色性色素-液晶分散方式、 膜方式、利用無色染料之 頁=色方式、光致變色方式、電子呈色方式、電沈積方 式、可撓性有飢方式等。電子紙不僅可為個人利用文本 或影像者’亦可用於廣告顯示(看板)等。根據本發明之光 學膜,可使電子紙之厚度變薄。 作為立體顯示裝置,例如提出有如咖(微偏光膜)方式 般交替排列不同相位差膜之方法(曰本專利特開2〇〇2- 185983破公報)’若使用本發明之光學膜作為偏光膜,則 藉由印刷、喷墨、光微影等進行圖案化較為容易故而可 縮短顯示裝置之製造步驟,且不需要相位差膜。 實施例 、下藉由貫施例更詳細地說明本發明,但本發明並不 限定於該等實施例。例中之「%」及「份」只要無特別記 載’則分別為質量%及質量份。 於實施例中,使用下述聚合性液晶化合物。 化合物(1-6)(下述式(1-6)所示之化合物) 化合物(1-6)The β cathode electrode 37 is formed by a vapor deposition method, a sputtering method, or the like, such as In Mg (Mg ′ 50 to 80 atom%) or Al.Ca (Ca: 5 to 20 atoms/0). The thickness of the cathode electrode 37 is preferably 0.1 nm or more, preferably nm to 5 〇〇 nm. The hole injection layer has a function of facilitating hole injection from the pixel electrode 35, and the hole transport layer has a function of transmitting a hole and a function of blocking electrons, which is also called a charge injection layer and a charge transport layer. The thickness of the light-emitting layer, the total thickness of the hole injection layer and the hole transport layer, and the thickness of the electron injection transport layer are not particularly limited, and are preferably set to 5 nm to 1 根据 depending on the method of formation. 〇nm. Hole injection layer, 158656.doc •32· 201224125 The hole transport layer allows the use of a variety of organic compounds. For the formation of the hole injection transport layer, the light-emitting layer and the electron injecting transport layer, it is preferred to use a vacuum evaporation method because a homogeneous film can be formed. The organic functional layer 36 as a light-emitting source can be used by those who emit light (fluorescence) derived from singlet excitons, those that emit light from phosphorous (phosphorescence) derived from triplet excitons, and those that utilize singlet excitons. An illuminating (fluorescent) person, an organic functional layer using a luminescence (phosphorescence) derived from a triplet exciton, a person formed by an organic substance, a person formed of an inorganic substance, a person formed by an organic substance, and an inorganic substance. Organic functional layer, polymer material, low molecular material, material containing molecular molecules and low molecular materials. However, it is not limited thereto, and a £1 display device using various organic functional layers can be used as the EL element. The desiccant is disposed in the space between the cathode electrode 37 and the sealing cover 39. The reason is that the organic functional layer 36 is not resistant to humidity. The desiccant 38 absorbs moisture to prevent deterioration of the organic functional layer 36. The EL display device 30 is formed. The polarizing film 31 on the light incident surface or the light exit surface is not limited to the polarizing film converted into linear polarized light, and may be a polarizing film converted into elliptically polarized light. The polarizing film 31 may be only the optical film of the present invention, or may be A polarizing film or a retardation film other than the optical film of the present invention is used in combination with Fig. 4. Fig. 4 is a schematic view showing a display device 44 which is one of the display devices of the present invention. The EL display device 44 has a film seal using # The sealing structure of the film core can also obtain light emitted from the opposite surface of the array substrate. As the film sealing film 42, it is preferable to use a DLC film on which a vapor deposition DLC (Diamond-like carbon) is deposited on a film of an electrolytic capacitor. The membrane system has extremely poor water permeability and high moisture resistance. X ' can also be directly vaporized from the DLC film to the surface of the cathode electrode 158656.doc -33· 201224125. Further, a multilayer resin film can be laminated. Metal film The film sealing film 42 is formed. At least one of the group consisting of the polarizing film 31 and the retardation film 32 is an optical film of the present invention. Fig. 5 is a view showing a projection type liquid crystal display device which is one of the display devices of the present invention. The polarizing film 142 of the present invention and the polarizing film 143 of the present invention can be used, for example, in a projection type liquid crystal display device (projector). A light beam emitted from a light source (for example, a high pressure mercury lamp) 111 as a light source first passes through the first lens array. 112. The second lens array 113, the polarization conversion element 114, and the superimposing lens 115 are used to uniformize and polarize the luminance on the beam cross section. Specifically, the beam emitted from the light source 111 is a small lens 112a. The first lens array 112 formed in a matrix is divided into a plurality of minute light beams. The second lens array 113 and the superimposing lens 115 illuminate the three liquid crystal panels 140R, 140G, and 140B to be illuminated, respectively, by the divided light beams. In a holistic manner, the illumination of the entire surface of the incident side surface of each liquid crystal panel is almost uniform. The polarization conversion element 114 includes a polarization beam splitter. The column is disposed between the second lens array 113 and the superimposing lens 115. This preliminarily converts the random polarized light from the light source into a polarized light having a specific polarization direction, thereby reducing the amount of light loss in the incident side polarizing element described below. The effect of increasing the brightness of the kneading surface. The light which is uniformized and polarized by the brightness is separated into red by the mirror 122 by the dichroic mirrors 121, 123, 132 for separating into the three primary colors of RGB. 158656.doc .14 - Λ 201224125 color channel ("R" in Figure 5, solid arrow), green channel ("G" in Figure 5, dotted arrow), blue channel ("B" in Figure 5] "dashed arrow" They are incident on the liquid crystal panels 140R, 140G, and 140B, respectively. In the liquid crystal panels 140R, 140G, and 140B, the polarizing element film 142 of the present invention is disposed on the incident side thereof, and the polarizing element film 143 of the present invention is disposed on the exit side. The polarizing film 142 and the polarizing film 143 disposed in the respective optical paths of RGB are arranged such that their absorption axes are orthogonal to each other. Each of the liquid crystal panels 140R, 140G, and 140B disposed in each of the optical paths has a function of converting the polarization state controlled by each pixel into a light amount by the image signal. The optical film of the present invention is used as an optical film excellent in durability in any of the blue channel, the green channel, and the red channel by selecting the type of the dichroic dye suitable for the corresponding channel. According to the respective image data of the liquid crystal panels 140R, 140G, and 14B, the optical image produced by transmitting the human light with different transmittances per pixel is synthesized by the combined light 稜鏡 15G, and the feeding mirror (7) is enlarged. On the projection screen 180. The optical film of the present invention can also be used as an electronic paper optical film. ::Electronic paper, which can be displayed by alignment of optically anisotropic material molecules such as liquid crystal; display by means of particle motion such as electrophoresis, particle movement, rotation, phase change, etc. ;_ &amp; eight &quot;, one of the end shifters, by the light absorption of the molecule, the display is not self-illuminating (4) ^ a by the electron and the hole is not obvious. As a specific display mode, 158656.doc -35- 201224125 List: microcapsule electrophoresis mode, dynamic electrophoresis mode, spherical twist-t-electrophoresis mode, vertical shift 4 round buckle... mode, magnetic torsional nematic ball Square;,=t mode, charged toner method, electronic powder fluid method, magnetic sensation method, electro-moisture method, light scattering (transparent/white turbidity change), cholesteric light scattering (transparent moon/liquid crystal mode, double Shirt (4); ^ type, cholesterol type... main, crystal mode, ferroelectric liquid crystal mode, dichroic dye-liquid crystal dispersion method, film method, page using colorless dye = color mode, photochromic mode, electronic coloration The method, the electrodeposition method, the flexibility, the hunger method, etc. The electronic paper can be used not only for individuals to use text or images, but also for advertisement display (kanban), etc. The optical film according to the present invention can change the thickness of the electronic paper. As a stereoscopic display device, for example, a method of alternately arranging different retardation films as in a coffee (micro-polarizing film) method has been proposed (Japanese Patent Laid-Open Publication No. 2 〇〇 2-185983). When the film is used as a polarizing film, patterning by printing, inkjet, photolithography, or the like is relatively easy, and the manufacturing process of the display device can be shortened, and a retardation film is not required. In the embodiment, the embodiment is described in more detail. The present invention is not limited to the examples, and the "%" and "parts" in the examples are respectively % by mass and parts by mass unless otherwise specified. In the examples, the following polymerization properties were used. Liquid crystal compound. Compound (1-6) (compound represented by the following formula (1-6)) Compound (1-6)

Bas’ 115’ 321-328 (1996)所記载之方法而合成。 158656.doc • 36 · 201224125Synthesized by the method described in Bas' 115' 321-328 (1996). 158656.doc • 36 · 201224125

一 CiiH^r-O [相轉移溫度之測定] 一面於形成有配向膜之玻璃基板上加熱化合物,一面藉 • 由利用偏光顯微鏡(BX-51,Olympus公司製造)之質構觀察 - 而確認相轉移溫度。式(1 _6)所示之化合物於升溫時,於 95°C下自結晶相呈現層列型A相,於1丨丨下相轉移為向列 相’於113 C下相轉移為等向性液體相《並且確認,於降 溫時,於112。(:下相轉移為向列相,於丨10°c下相轉移為層 列型A相,於94°C下相轉移為層列型b相。 化合物(1-7)(下述式(1-7)所示之化合物) 化合物(1-7)係依據.1^1^6131.,尺6〇1.!^乂.0!11丨111.?&amp;3^-Bas,115, 321-328 (1996)所記載之方法而合成。CiiH^rO [Measurement of phase transition temperature] The phase transition temperature was confirmed by heating a compound on a glass substrate on which an alignment film was formed, by observation using a polarizing microscope (BX-51, manufactured by Olympus). . The compound represented by the formula (1-6) exhibits a smectic phase A phase at a temperature of 95 ° C at a temperature of 95 ° C, and a phase transition to a nematic phase at 113 C to an isotropic property at 113 C. The liquid phase "and confirms that at the time of cooling, at 112. (: The lower phase is transferred to the nematic phase, and the phase is transferred to the smectic A phase at 10 ° C, and the phase is transferred to the smectic phase b phase at 94 ° C. Compound (1-7) (the following formula ( 1-7) The compound (1-7) is based on .1^1^6131., 6〇1.!^乂.0!11丨111.?&amp;3^-Bas,115, Synthesized by the method described in 321-328 (1996).

[相轉移溫度之測定] 藉由利用偏光顯微鏡之質構觀察而確認相轉移溫度。式 (1-7)所示之化合物於升溫時’於8rc下自結晶相呈現層列 型A相’於12rc下轉移為向列相,於i37°C下相轉移為等 向性液體相。並且確認,於降溫時,於13 3。(:下相轉移為 向列相,於118°C下相轉移為層列型A相,於78°C下相轉移 為層列型B相。 實施例1 I58656.doc -37· 201224125 [聚合性液晶組合物之製備] 藉由混合下述成分,並將所得之混合物於80°C下搜拌1 小時,而獲得聚合性液晶組合物。 聚合性液晶化合物:化合物(1-6) 100份 二色性色素:偶氮色素(NKX2029,林原生物化學研究 所製造)2份 聚合起始劑:2-二曱胺基-2-节基-1 -(4-嗎琳基苯基)丁 烧-1-酮(Irgacure 369,BASF Japan公司製造)6份 聚合起始助劑:異丙基噻噸酮(日本Siber Hegner公司製 造)2份 調平劑:聚丙烯酸酯化合物(BYK-361N,BYK-Chemie 公司製造)1.2份 溶劑:環戊酮250份 [光學膜之製作] 藉由旋轉塗佈法於玻璃基板上塗佈聚乙烯醇(聚乙烯醇 1000完全皂化型,和光純藥工業股份有限公司製造)之2質 量%水溶液,乾燥後,形成厚度為89 nm之配向膜。繼 而,對所得之配向膜之表面實施摩擦處理。摩擦處理係使 用半自動摩擦裝置(商品名:LQ-008型,常陽工學股份有 限公司製造),利用布(商品名:YA-20-RW,吉川化工股份 有限公司製造),於壓入量0.15 mm、轉速500 rpm、16.7 mm/s之條件下進行。 藉由旋轉塗佈法於摩擦後之配向膜上塗佈聚合性液晶組 合物,於12 (TC之加熱板上加熱乾燥3分鐘後,迅速冷卻至 158656.doc . 38 - 201224125 70°C (於降溫時顯示層列相之溫度),獲得乾燥後塗膜。藉 由使用UV照射裝置(SP0T clJRE SP_7,Ushio電機股份有 限公司製造),對乾燥後塗膜照射曝光量24〇〇 mJ/cm2(365 run基準)之紫外線照射,獲得製作於玻璃基板上之光學 膜。 [二色比之測定] 使用於島津製作所製造之紫外可見分光光度計UV_3丨5〇 上安裝有附帶偏光元件之摺疊器的裝置,藉由雙波束法測 定極大吸收波長下之透射軸方向之吸光度(Al)及吸收轴方 向之吸光度(A2)。該摺疊器係於參考侧設置使光量減少 50%之篩網。根據所測定之透射軸方向之吸光度(Al)及吸 收軸方向之吸光度(A2)之值算出比(a2/a1),設為二色比。 將結果示於表2»可認為二色比越高,作為偏光膜越有 用。 [膜厚測定] 針對所得之光學膜,使用雷射顯微鏡(LEXT3〇〇〇, Olympus公司製造)測定膜厚。將結果示於表2。 [霧度之測定] 針對所得之光學膜,使用霧度計(HZ-2,Suga試驗機 (股)製造)測定霧度值。將結果示於表2。 [液晶相之觀察] 針對所得之光學膜所顯示之液晶相,使用偏光顯微鏡 (ΒΧ·51,Olympus公司製造)進行觀察。觀察係以於透射軸 交之2片偏光元件之間,相對於偏光元件之透射軸成為 158656.doc •39- 201224125 45°之方向之方式配置所得之光學膜之遲相軸而進行。 觀察之結果,將可見形成水平配向單域者設為〇,將未 見形成水平配向單域者設為x。將結果示於表2。 [不均之觀察] 針對所得之光學膜,以吸收軸與碘-PVA偏光板 (SRW842A,住友化學(股)製造)正交之方式進行配置,於 直下型背光裝置上進行目測觀察。將未觀察到相分離狀之 不均者設為〇,將觀察到相分離狀之不均者設為X。將結果 示於表2。 實施例2〜15、參考例1及2 使用表1所示之聚合性液晶化合物及調平劑,以與實施 例1相同之方式進行實施,而獲得聚合性液晶組合物。 [表1] 聚合性液晶化合物 調平劑(份) 實施例1 化合物(1-6) BYK-361N(1.2) 實施例2 化合物(1-6) BYK-361N(0.6) 實施例3 化合物(1-6) BYK-361N(1) 實施例4 化合物(1-6) BYK-361N(1.5) 實施例5 化合物(1-6) BYK-361N(2) 實施例6 化合物(1-6) BYK-361N(2.5) 實施例7 化合物(1-6) BYK-361N(3) 實施例8 化合物(1-6) BYK-352(1.2) 實施例9 化合物(1-6) BYK-354(1.3) 158656.doc -40. 201224125 實施例10 化合物(1-6) BYK-381(1.3) 實施例11 化合物(1-6) BYK-392(1.1) 實施例12 化合物(1-6) F471(l.l) 實施例13 化合物(1-6) F477(l.l) 實施例14 化合物(1-7) BYK-361N(1.2) 實施例15 化合物(1-7) F471(2) 參考例1 化合物(1-6) BYK-361N(0.2) 參考例2 化合物(1-6) BYK-361N(5.2) 表1中所示之調平劑係使用以下者。 聚丙烯酸酯化合物(BYK-361N,BYK-Chemie公司製造) 聚丙烯酸酯化合物(BYK-3 52,BYK-Chemie公司製造) 聚丙烯酸酯化合物(BYK-354,BYK-Chemie公司製造) 聚丙烯酸酯化合物(BYK-381,BYK-Chemie公司製造) 聚丙烯酸酯化合物(BYK-392,BYK-Chemie公司製造) 含氟之低聚物(Megafac F471,DIC(股)製造) 含氟之低聚物(Megafac F477,DIC(股)製造) 針對上述所得之實施例2〜15、參考例1及2之聚合性液晶 組合物,以與實施例1相同之方式進行評價。將結果示於 表2。 158656.doc -41 - 201224125 [表2] 二色比 極大吸收波 長(μτη) 霧度 液晶 相 不均 膜厚(μτη) 實施例1 34 520 1.5% 〇 〇 1.8 實施例2 23 520 1.8% 〇 〇 1.8 實施例3 26 520 1.5% 〇 〇 1.8 實施例4 31 520 1.1% 〇 〇 1.8 實施例5 29 520 0.9% 〇 〇 1.8 實施例6 29 520 0.9% 〇 〇 1.8 實施例7 33 520 0.7% 〇 〇 1.8 實施例8 35 520 0.4% 〇 〇 1.8 實施例9 33 520 0.8% 〇 〇 1.8 實施例10 29 520 1.2% 〇 〇 1.8 實施例11 33 520 0.6% 〇 〇 1.8 實施例12 32 520 0.7% 〇 〇 1.8 實施例13 31 520 1.3% 〇 〇 1.8 實施例14 30 520 2.4% 〇 0 1.8 實施例15 30 520 1.8% 〇 〇 1.8 參考例1 2 520 9.3% X 〇 1.8 參考例2 14 520 5.2% 〇 X 1.8 實施例16 [聚合性液晶組合物之製備] 藉由混合下述成分,並將所得之混合物於80°C下攪拌1 小時,而獲得聚合性液晶組合物。 聚合性液晶化合物:化合物(1_6) 100份 158656.doc • 42· 201224125 聚合起始劑:2-二甲胺基-2-节基-by—嗎啉基苯基)丁 烧-l-_(Irgacure 369,BASF Japan公司製造)6份 聚&amp;起始助劑.異丙基嘆嘲綱(曰本Siber Hegner公司製 造)2份 調平劑.聚丙烯酸酯化合物(BYK-361N,BYK_Chemie 公司製造)1.2份 溶劑:環戊酮25 0份 [光學膜之製作] 使用上述所獲得之聚合性液晶組合物,以與實施例i相 同之方式進行實施,而獲得光學膜。 [液晶相之觀察] 針對所得之光學膜,以與實施例丨相同之方式進行液晶 相之觀察’結果可見形成水平配向單域。 [膜厚之測定] 針對所得之光學膜’以與實施例1相同之方式測定膜 厚’結果為1.8 μιη。 [相位差值之測定] 針對所得之光學膜,使用雙折射測定裝置(K0BRA_ WR,王子計測機器公司製造)測定波長“八?打瓜下之表面 相位差值,結果為257 nm。再者,由於用作基材之玻璃基 板不具有雙折射性,故而藉由利用測定機計測附帶玻璃基 板之狀態之光學膜,可獲得光學膜之表面相位差值。 [產業上之可利用性] 根據本發明之聚合性液晶組合物,可容易地獲得形成有 158656.doc -43- 201224125 丁…己向之層列相的光學膜。由於形成有向水平方 向配向之層列相且含有二色性色素之光學膜尤其於二色比 方面優異,故而作為偏光膜有用。 【圖式簡單說明】 圖1係表示作為本發明之顯示裝置之一的液晶顯示裝置 10的概略圖。 圖2係表示作為本發明之顯示裝置之一的液晶顯示裝置 24的概略圖。 圖3係表示作為本發明之顯示裝置之一的EL顯示裝置30 的概略圖。 圖4係表示作為本發明之顯示裝置之一的EL顯示裝置44 的概略圖。 圖5係表示作為本發明之顯示裝置之一的投射型液晶顯 示裝置的概略圖。 【主要元件符號說明】 10 液晶顯示裝置 11 抗反射膜 12a 偏光膜 12b 偏光膜 13a 相位差膜 13b 相位差膜 14a 基板 14b 基板 15 彩色濾光片 158656.doc -44 - 201224125 16 透明電極 17 液晶層 18 層間絕緣膜 19 背光單元 20 黑矩陣 21 薄膜電晶體 22 像素電極 23 間隔物 24 液晶顯示裝置 30 EL顯示裝置 31 偏光膜 32 相位差膜 33 基板 34 層間絕緣膜 35 像素電極 36 發光層 37 陰極電極 38 乾燥劑 39 密封蓋 40 薄膜電晶體 41 阻隔壁 42 薄膜密封膜 44 EL顯示裝置 111 光源 158656.doc -45- 201224125 112 第1透鏡陣列 112a 透鏡 113 第2透鏡陣列 114 偏光轉換元件 115 重疊透鏡 121 雙色鏡 122 反射鏡 123 雙色鏡 132 雙色鏡 140R 液晶面板 140G 液晶面板 140B 液晶面板 142 偏光膜 143 偏光膜 150 合光棱鏡 170 投影透鏡 180 屏幕 B 藍通道 G 綠色通道 R 紅色通道 158656.doc -46-[Measurement of Phase Transition Temperature] The phase transition temperature was confirmed by observation using a texture of a polarizing microscope. The compound of the formula (1-7) was transferred to a nematic phase at 12 rc at a temperature of 8 rc at a temperature of 8 rc, and the phase was transferred to an isotropic liquid phase at i37 °C. And confirm that when cooling, at 13 3 . (The lower phase is transferred to the nematic phase, and the phase is transferred to the smectic A phase at 118 ° C, and the phase is transferred to the smectic phase B phase at 78 ° C. Example 1 I58656.doc -37· 201224125 [Polymerization Preparation of liquid crystal composition] A polymerizable liquid crystal composition was obtained by mixing the following components and mixing the resulting mixture at 80 ° C for 1 hour. Polymerizable liquid crystal compound: Compound (1-6) 100 parts Dichroic dye: azo dye (NKX2029, manufactured by Hayashibara Biochemical Research Institute) 2 parts polymerization initiator: 2-diaminoamino-2-pyryl-1 -(4-morphinylphenyl)butane 1-ketone (Irgacure 369, manufactured by BASF Japan) 6 parts of polymerization starting aid: isopropyl thioxanthone (manufactured by Siber Hegner, Japan) 2 parts of leveling agent: polyacrylate compound (BYK-361N, BYK) -Chemie company's 1.2 parts solvent: 250 parts of cyclopentanone [production of optical film] Polyvinyl alcohol (polyvinyl alcohol 1000 completely saponified type) is coated on a glass substrate by spin coating method, and the company is limited. A 2% by mass aqueous solution manufactured by the company, after drying, forms an alignment film having a thickness of 89 nm. The surface of the obtained alignment film is subjected to a rubbing treatment. The friction treatment is performed by using a semi-automatic friction device (trade name: LQ-008 type, manufactured by Changyang Engineering Co., Ltd.), and the cloth is used (trade name: YA-20-RW, Yoshikawa Chemical Co., Ltd.) Co., Ltd.), under the conditions of 0.15 mm, 500 rpm, and 16.7 mm/s. The polymerizable liquid crystal composition is coated on the alignment film after rubbing by spin coating at 12 (TC). After heating and drying on a hot plate for 3 minutes, it is rapidly cooled to 158656.doc. 38 - 201224125 70 ° C (the temperature of the smectic phase is displayed when the temperature is lowered), and the film after drying is obtained. By using a UV irradiation device (SP0T clJRE) SP_7, manufactured by Ushio Electric Co., Ltd.), irradiated with ultraviolet light of an exposure amount of 24 μm/cm 2 (365 run basis) after drying, to obtain an optical film produced on a glass substrate. [Measurement of two-color ratio] A device equipped with a folder with a polarizing element was mounted on an ultraviolet-visible spectrophotometer UV_3丨5〇 manufactured by Shimadzu Corporation, and the absorption direction of the transmission axis at the maximum absorption wavelength was measured by the double beam method. Degree (Al) and absorbance in the absorption axis direction (A2). The folder is provided with a screen for reducing the amount of light by 50% on the reference side. The absorbance (Al) in the direction of the transmission axis measured and the absorbance in the direction of the absorption axis ( The value of A2) is calculated as a ratio (a2/a1), and is a dichroic ratio. The results are shown in Table 2»The higher the dichroic ratio is, the more useful it is as a polarizing film. [Measurement of film thickness] For the obtained optical film, The film thickness was measured using a laser microscope (LEXT3®, manufactured by Olympus Co., Ltd.). The results are shown in Table 2. [Measurement of haze] The haze value of the obtained optical film was measured using a haze meter (HZ-2, manufactured by Suga Tester Co., Ltd.). The results are shown in Table 2. [Observation of Liquid Crystal Phase] The liquid crystal phase displayed on the obtained optical film was observed using a polarizing microscope (ΒΧ·51, manufactured by Olympus Co., Ltd.). The observation is performed by arranging the retardation axes of the obtained optical films with respect to the transmission axis of the polarizing element between the two polarizing elements of the transmission axis in a direction of 158656.doc • 39 - 201224125 45°. As a result of the observation, it is seen that the person who forms the horizontal alignment single domain is set to 〇, and the person who does not form the horizontal alignment single domain is set to x. The results are shown in Table 2. [Observation of unevenness] The obtained optical film was placed so as to be orthogonal to the iodine-PVA polarizing plate (SRW842A, manufactured by Sumitomo Chemical Co., Ltd.), and visually observed on a direct type backlight device. When the unevenness of the phase separation was not observed, it was set to 〇, and the unevenness of the phase separation was observed to be X. The results are shown in Table 2. Examples 2 to 15 and Reference Examples 1 and 2 Polymerizable liquid crystal compounds and a leveling agent shown in Table 1 were used in the same manner as in Example 1 to obtain a polymerizable liquid crystal composition. [Table 1] Polymerizable liquid crystal compound leveling agent (part) Example 1 Compound (1-6) BYK-361N (1.2) Example 2 Compound (1-6) BYK-361N (0.6) Example 3 Compound (1) -6) BYK-361N (1) Example 4 Compound (1-6) BYK-361N (1.5) Example 5 Compound (1-6) BYK-361N (2) Example 6 Compound (1-6) BYK- 361N (2.5) Example 7 Compound (1-6) BYK-361N (3) Example 8 Compound (1-6) BYK-352 (1.2) Example 9 Compound (1-6) BYK-354 (1.3) 158656 .doc -40. 201224125 Example 10 Compound (1-6) BYK-381 (1.3) Example 11 Compound (1-6) BYK-392 (1.1) Example 12 Compound (1-6) F471 (ll) Example 13 Compound (1-6) F477 (11) Example 14 Compound (1-7) BYK-361N (1.2) Example 15 Compound (1-7) F471 (2) Reference Example 1 Compound (1-6) BYK -361N (0.2) Reference Example 2 Compound (1-6) BYK-361N (5.2) The leveling agent shown in Table 1 used the following. Polyacrylate compound (BYK-361N, manufactured by BYK-Chemie Co., Ltd.) Polyacrylate compound (BYK-3 52, manufactured by BYK-Chemie Co., Ltd.) Polyacrylate compound (BYK-354, manufactured by BYK-Chemie) Polyacrylate compound (BYK-381, manufactured by BYK-Chemie) Polyacrylate compound (BYK-392, manufactured by BYK-Chemie) Fluorine-containing oligomer (Megafac F471, manufactured by DIC) Fluorine-containing oligomer (Megafac F477, DIC (manufactured by DIC) The polymerizable liquid crystal compositions of Examples 2 to 15 and Reference Examples 1 and 2 obtained above were evaluated in the same manner as in Example 1. The results are shown in Table 2. 158656.doc -41 - 201224125 [Table 2] Dichromatic ratio Maximum absorption wavelength (μτη) Haze liquid crystal phase uneven film thickness (μτη) Example 1 34 520 1.5% 〇〇1.8 Example 2 23 520 1.8% 〇〇 1.8 Example 3 26 520 1.5% 〇〇 1.8 Example 4 31 520 1.1% 〇〇 1.8 Example 5 29 520 0.9% 〇〇 1.8 Example 6 29 520 0.9% 〇〇 1.8 Example 7 33 520 0.7% 〇〇 1.8 Example 8 35 520 0.4% 〇〇 1.8 Example 9 33 520 0.8% 〇〇 1.8 Example 10 29 520 1.2% 〇〇 1.8 Example 11 33 520 0.6% 〇〇 1.8 Example 12 32 520 0.7% 〇〇 1.8 Example 13 31 520 1.3% 〇〇1.8 Example 14 30 520 2.4% 〇0 1.8 Example 15 30 520 1.8% 〇〇1.8 Reference Example 1 2 520 9.3% X 〇1.8 Reference Example 2 14 520 5.2% 〇X 1.8 Example 16 [Preparation of polymerizable liquid crystal composition] A polymerizable liquid crystal composition was obtained by mixing the following components and stirring the resulting mixture at 80 ° C for 1 hour. Polymerizable liquid crystal compound: compound (1_6) 100 parts 158656.doc • 42· 201224125 Polymerization initiator: 2-dimethylamino-2-pyryl-by-morpholinylphenyl) butanol-l-_ ( Irgacure 369, manufactured by BASF Japan) 6 parts poly &amp; starting aid. Isopropyl sneak (manufactured by Siber Hegner) 2 parts of leveling agent. Polyacrylate compound (BYK-361N, manufactured by BYK_Chemie) 1.2 parts of solvent: 25 parts of cyclopentanone [Production of optical film] Using the polymerizable liquid crystal composition obtained above, it was carried out in the same manner as in Example i to obtain an optical film. [Observation of liquid crystal phase] With respect to the obtained optical film, observation of the liquid crystal phase was carried out in the same manner as in Example ’, and it was found that a horizontal alignment single domain was formed. [Measurement of film thickness] The film thickness was measured in the same manner as in Example 1 for the obtained optical film'. The result was 1.8 μm. [Measurement of the phase difference value] The surface retardation value of the wavelength "eight?" was measured using a birefringence measuring apparatus (K0BRA_WR, manufactured by Oji Scientific Instruments Co., Ltd.), and the result was 257 nm. Since the glass substrate used as the substrate does not have birefringence, the surface retardation value of the optical film can be obtained by measuring the optical film in a state in which the glass substrate is attached by the measuring device. [Industrial Applicability] According to the present invention In the polymerizable liquid crystal composition of the invention, an optical film having a stratified phase formed by 158656.doc -43 - 201224125 can be easily obtained, and a smectic phase which is aligned in the horizontal direction is formed and contains a dichroic dye. The optical film is particularly useful as a polarizing film, and is useful as a polarizing film. [Brief Description of the Drawings] Fig. 1 is a schematic view showing a liquid crystal display device 10 which is one of the display devices of the present invention. A schematic diagram of a liquid crystal display device 24 which is one of the display devices of the present invention. Fig. 3 is a schematic view showing an EL display device 30 which is one of the display devices of the present invention. Fig. 5 is a schematic view showing a projection type liquid crystal display device which is one of the display devices of the present invention. [Description of main components] 10 Liquid crystal display device 11 Antireflection film 12a Polarizing film 12b Polarizing film 13a Phase difference film 13b Phase difference film 14a Substrate 14b Substrate 15 Color filter 158656.doc -44 - 201224125 16 Transparent electrode 17 Liquid crystal layer 18 Interlayer insulating film 19 Backlight unit 20 Black matrix 21 Thin film transistor 22 pixel electrode 23 spacer 24 liquid crystal display device 30 EL display device 31 polarizing film 32 retardation film 33 substrate 34 interlayer insulating film 35 pixel electrode 36 light emitting layer 37 cathode electrode 38 desiccant 39 sealing cover 40 thin film transistor 41 Barrier wall 42 Membrane sealing film 44 EL display device 111 Light source 158656.doc -45- 201224125 112 1st lens array 112a Lens 113 2nd lens array 114 Polarization conversion element 115 Overlapping lens 121 Bi-color mirror 122 Mirror 123 Bi-color mirror 132 Bi-color mirror 140R LCD panel 140G LCD panel 140 B Liquid crystal panel 142 Polarizing film 143 Polarizing film 150 Light-emitting prism 170 Projection lens 180 Screen B Blue channel G Green channel R Red channel 158656.doc -46-

Claims (1)

201224125 七、申請專利範圍: 1.種聚合性液晶組合物’其係含有顯示層列相之聚合性 液晶化合物、調平劑及溶劑者,並且調平劑係選自由以 聚丙烯酸酯化合物為主成分之調平劑及以含氟原子之化 合物為主成分之調平劑所組成之群中之至少1種,調平 劑之含1相對於聚合性液晶化合物1〇〇質量份為〇 3質量 份以上且5質量份以下。 2. 如凊求項1之聚合性液晶組合物,其中聚合性液晶化合 物係於帛示層列相之溫度與顯示等向相之溫度之間顯示 向列相。 3. 如咕求項1之聚合性液晶組合物,其進而含有二色性色 素。 種光學膜’其係藉由使如請求項【至〗中任一項之聚合 性液晶組合物中所含之聚合性液晶化合物聚合而獲得。 5·種光學膜之製造方法,其包括下述步驟⑴、步驟⑺ 及步驟(3): 步驟⑴·將如請求項i至3中任一項之聚合性液晶組合 物塗佈於基板上而獲得塗佈膜之步驟; '驟(2).於步驟⑴中獲得之塗佈膜中形成液晶相之 步驟; =(3):藉由使步驟⑺中獲得之形成有液晶相之膜 所3之聚合性液晶化合物聚纟而獲得光學膜之步驟。 ,士月求項5之製造方法,其中液晶相為層列相。 / 士請求項5之製造方法,其中步驟⑺係藉由將步驟⑴中 158656.doc 201224125 獲得之塗佈膜加熱至塗佈膜中所含之聚合性液晶化合物 轉移至向列相之溫度以上,繼而將該聚合性液晶化合物 冷卻至顯示層列相之溫度,而獲得該聚合性液晶化合物 配向為層列相之膜的步驟。 8. —種顯示裝置’其含有如請求項4之光學膜。 9. 一種顯示裝置,其含有藉由如請求項5之製造方法而獲 得之光學膜。 10. —種顯示裝置’其含有藉由如請求項6或7之製造方法而 獲得之光學膜。 158656.doc201224125 VII. Patent application scope: 1. A polymerizable liquid crystal composition which contains a polymerizable liquid crystal compound, a leveling agent and a solvent which exhibit a phase of a layer, and the leveling agent is selected from a polyacrylate compound. At least one of a group consisting of a leveling agent of a component and a leveling agent containing a fluorine atom-containing compound as a main component, and the content of the leveling agent is 1 质量3 by mass based on 1 part by mass of the polymerizable liquid crystal compound. More than 5 parts by weight. 2. The polymerizable liquid crystal composition according to claim 1, wherein the polymerizable liquid crystal compound exhibits a nematic phase between a temperature of the column phase of the display layer and a temperature of the isotropic phase. 3. The polymerizable liquid crystal composition of claim 1, which further comprises a dichroic colorant. The optical film is obtained by polymerizing a polymerizable liquid crystal compound contained in the polymerizable liquid crystal composition according to any one of the above claims. A method for producing an optical film, comprising the following steps (1), (7), and (3): Step (1): applying the polymerizable liquid crystal composition according to any one of claims 1 to 3 to a substrate. a step of obtaining a coating film; 'Step (2). a step of forming a liquid crystal phase in the coating film obtained in the step (1); = (3): a film having a liquid crystal phase formed by the step (7) The polymerizable liquid crystal compound is agglomerated to obtain an optical film. The manufacturing method of the item 5, wherein the liquid crystal phase is a smectic phase. The manufacturing method of claim 5, wherein the step (7) is carried out by heating the coating film obtained in the step (1) of 158656.doc 201224125 until the polymerizable liquid crystal compound contained in the coating film is transferred to a temperature above the nematic phase. Then, the polymerizable liquid crystal compound is cooled to a temperature of the display layer column phase to obtain a step of aligning the polymerizable liquid crystal compound into a film of a smectic phase. 8. A display device 'which contains the optical film of claim 4. A display device comprising the optical film obtained by the production method of claim 5. 10. A display device' which comprises an optical film obtained by the manufacturing method of claim 6 or 7. 158656.doc
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