JP5591451B2 - 液晶媒体 - Google Patents
液晶媒体 Download PDFInfo
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- JP5591451B2 JP5591451B2 JP2008031476A JP2008031476A JP5591451B2 JP 5591451 B2 JP5591451 B2 JP 5591451B2 JP 2008031476 A JP2008031476 A JP 2008031476A JP 2008031476 A JP2008031476 A JP 2008031476A JP 5591451 B2 JP5591451 B2 JP 5591451B2
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- 239000004973 liquid crystal related substance Substances 0.000 title claims description 61
- 150000001875 compounds Chemical class 0.000 claims description 115
- 125000000217 alkyl group Chemical group 0.000 claims description 40
- 125000004432 carbon atom Chemical group C* 0.000 claims description 26
- 125000003342 alkenyl group Chemical group 0.000 claims description 17
- 230000000694 effects Effects 0.000 claims description 15
- 239000011159 matrix material Substances 0.000 claims description 12
- 229910052731 fluorine Inorganic materials 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 10
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
- YCLAMANSVUJYPT-UHFFFAOYSA-L aluminum chloride hydroxide hydrate Chemical compound O.[OH-].[Al+3].[Cl-] YCLAMANSVUJYPT-UHFFFAOYSA-L 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims 4
- 239000000203 mixture Substances 0.000 description 53
- 238000005516 engineering process Methods 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 210000004027 cell Anatomy 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 7
- -1 methoxy, ethoxy, propoxy, butoxy Chemical group 0.000 description 7
- 230000004044 response Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000004990 Smectic liquid crystal Substances 0.000 description 5
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 4
- 101150065749 Churc1 gene Proteins 0.000 description 4
- 239000004988 Nematic liquid crystal Substances 0.000 description 4
- 102100038239 Protein Churchill Human genes 0.000 description 4
- 235000010290 biphenyl Nutrition 0.000 description 4
- 150000004074 biphenyls Chemical class 0.000 description 4
- 150000002367 halogens Chemical group 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 150000001911 terphenyls Chemical class 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000002019 doping agent Substances 0.000 description 3
- 230000005684 electric field Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical class C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 2
- WVIIMZNLDWSIRH-UHFFFAOYSA-N cyclohexylcyclohexane Chemical class C1CCCCC1C1CCCCC1 WVIIMZNLDWSIRH-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- SJSRFXJWBKOROD-UHFFFAOYSA-N 1,1'-bi(cyclohexyl)-1-carboxylic acid Chemical class C1CCCCC1C1(C(=O)O)CCCCC1 SJSRFXJWBKOROD-UHFFFAOYSA-N 0.000 description 1
- PKORYTIUMAOPED-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinazoline Chemical compound C1=CC=C2NCNCC2=C1 PKORYTIUMAOPED-UHFFFAOYSA-N 0.000 description 1
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
- RAYZALBEMJMGEA-UHFFFAOYSA-N 1-cyclohexylnaphthalene Chemical class C1CCCCC1C1=CC=CC2=CC=CC=C12 RAYZALBEMJMGEA-UHFFFAOYSA-N 0.000 description 1
- KGFKYWUYESESLF-UHFFFAOYSA-N 2,2-difluoro-3,4-dihydrophenanthro[9,10-b]pyran Chemical class C12=CC=CC=C2C2=CC=CC=C2C2=C1OC(F)(F)CC2 KGFKYWUYESESLF-UHFFFAOYSA-N 0.000 description 1
- SMHSPYVJAUGNOI-UHFFFAOYSA-N 2-cyclohexyl-1,4-dioxane Chemical class C1CCCCC1C1OCCOC1 SMHSPYVJAUGNOI-UHFFFAOYSA-N 0.000 description 1
- YJDDXMSIMBMMGY-UHFFFAOYSA-N 2-cyclohexylpyrimidine Chemical class C1CCCCC1C1=NC=CC=N1 YJDDXMSIMBMMGY-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 229940123457 Free radical scavenger Drugs 0.000 description 1
- 101150055539 HADH gene Proteins 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 241000620457 Telestes souffia Species 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000001482 benzyl phenyl ethers Chemical class 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 150000001851 cinnamic acid derivatives Chemical class 0.000 description 1
- 150000003983 crown ethers Chemical class 0.000 description 1
- 210000002858 crystal cell Anatomy 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- DQZKGSRJOUYVPL-UHFFFAOYSA-N cyclohexyl benzoate Chemical class C=1C=CC=CC=1C(=O)OC1CCCCC1 DQZKGSRJOUYVPL-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000532 dioxanyl group Chemical group 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- RBBNOVKRLWDEGC-UHFFFAOYSA-M dodecyl-ethyl-dimethylazanium;4-hexoxybenzoate Chemical compound CCCCCCOC1=CC=C(C([O-])=O)C=C1.CCCCCCCCCCCC[N+](C)(C)CC RBBNOVKRLWDEGC-UHFFFAOYSA-M 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000013213 extrapolation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000012826 global research Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 101150054634 melk gene Proteins 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 1
- UVEWQKMPXAHFST-UHFFFAOYSA-N n,1-diphenylmethanimine Chemical class C=1C=CC=CC=1C=NC1=CC=CC=C1 UVEWQKMPXAHFST-UHFFFAOYSA-N 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000005361 soda-lime glass Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 150000001629 stilbenes Chemical class 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
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- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/10—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
- C09K19/12—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
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- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
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- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3098—Unsaturated non-aromatic rings, e.g. cyclohexene rings
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- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/32—Non-steroidal liquid crystal compounds containing condensed ring systems, i.e. fused, bridged or spiro ring systems
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- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/42—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
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- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/0403—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit the structure containing one or more specific, optionally substituted ring or ring systems
- C09K2019/0407—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit the structure containing one or more specific, optionally substituted ring or ring systems containing a carbocyclic ring, e.g. dicyano-benzene, chlorofluoro-benzene or cyclohexanone
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- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/10—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
- C09K19/12—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
- C09K2019/121—Compounds containing phenylene-1,4-diyl (-Ph-)
- C09K2019/123—Ph-Ph-Ph
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- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
- C09K2019/3004—Cy-Cy
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- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
- C09K2019/301—Cy-Cy-Ph
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- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
- C09K2019/3016—Cy-Ph-Ph
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- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
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- Liquid Crystal Substances (AREA)
- Liquid Crystal (AREA)
Description
R1AおよびR1Bは、それぞれ互いに独立に、6個までの炭素原子を有するアルケニル基を表し、該基は置換されていないか、CNまたはCF3によって1置換されているか、またはハロゲンによって少なくとも1置換されており、ただし加えて、これらの基の中の1個以上のCH2基は、酸素原子が互いに直接結合しないようにして、−O−、−S−、
−C≡C−、−CF2O−、−OCF2−、−OC−O−または−O−CO−で置き換えられていてもよく、
R2A、R2B、R1C、R1DおよびR2Dは、それぞれ互いに独立に、6個までの炭素原子を有するアルキルまたはアルケニル基を表し、該基は置換されていないか、CNまたはCF3によって1置換されているか、またはハロゲンによって少なくとも1置換されており、ただし加えて、これらの基の中の1個以上のCH2基は、酸素原子が互いに直接結合しないようにして、−O−、−S−、
Y3は、HまたはCH3を表し、
R2Cは、HまたはFを表し、
R3Cは、H、CH3、C2H5またはn−C3H7を表し、
aおよびbは、それぞれ互いに独立に、0、1または2を表し、ただしa+bは1以上であり、
cは、1または2を表し、および
dは、0または1を表す。
M.F.SchieckelおよびK.Fahrenschon、「Deformation of nematic liquid crystals with vertical orientation in electrical fields」、Appl.Phys.Lett.19(1971)、3912 J.F.Kahn、Appl.Phys.Lett.20(1972)、1193 G.LabrunieおよびJ.Robert、J.Appl.Phys.44(1973)、4869 J.RobertおよびF.Clerc、SID 80 Digest Techn.Papers(1980)、30 J.Duchene、Displays 7(1986)、3 H.Schad、SID 82 Digest Techn.Papers(1982)、244 Yoshide、H.ら、論文3.1:「MVA LCD for Notebook or Mobile PCs・・・」SID 2004 International Symposium、Digest of Technical Papers、XXXV、Book I、第6〜9頁 Liu、C.T.ら、論文15.1:「A 46−inch TFT−LCD HDTV Technology・・・」、SID 2004 International Symposium、Digest of Technical Papers、XXXV、Book II、第750〜753頁 Kim、Sang Soo、論文15.4:「Super PVA Sets New State−of−the−Art for LCD−TV」、SID 2004 International Symposium、Digest of Technical Papers、XXXV、Book II、第760〜763頁 Shigeta、MitzuhiroおよびFukuoka、Hirofumi、論文15.2:「Development of High Quality LCDTV」、SID 2004 International Symposium、Digest of Technical Papers、XXXV、Book II、第754〜757頁 Yeo、S.D.、論文15.3:「An LC Display for the TV Application」、SID 2004 International Symposium、Digest of Technical Papers、XXXV、Book II、第758および759頁 Souk、Jun、セミナーM−6:「Recent Advances in LCD Technology」、セミナー講義ノート、M−6/1〜M−6/26 Miller、Ian、SIDセミナー 2004、セミナーM−7:「LCD−Television」、セミナー講義ノート、M−7/1〜M−7/32 Kim、Hyeon Kyeongら、論文9.1:「A57−in.Wide UXGA TFT−LCD for HDTV Application」、SID 2004 International Symposium、Digest of Technical Papers、XXXV、Book I、第106〜109頁 TOGASHI,S.、SEKIGUCHI,K.、TANABE,H.、YAMAMOTO,E.、SORIMACHI,K.、TAJIMA,E.、WATANABE,H.およびSHIMIZU,H.、Proc.Eurodisplay、1984年9月、第84巻、第A210〜288号、「Matrix LCD Controlled by Double Stage Diode Rings」、第141ff頁(パリ) STROMER,M.、Proc.Eurodisplay、第84巻、1984年9月、「Design of Thin Film Transistors for Matrix Addressing of Television Liquid Crystal Displays」、第145ff頁(パリ)
Y1=Cl、Y2=FおよびY3=H。
R2は、Hまたは15個までの炭素原子を有するアルキルまたはアルケニル基(好ましくはアルキル基)を表し、該基は置換されていないか、CNまたはCF3によって1置換されているか、またはハロゲンによって少なくとも1置換されており、ただし加えて、これらの基の中の1個以上のCH2基は、酸素原子が互いに直接結合しないようにして、−O−、−S−、
L1〜4は、それぞれ互いに独立に、FまたはClを表し、
Z2は、単結合、−CH2CH2−、−CH=CH−、−CF2O−、−OCF2−、−CH2O−、−OCH2−、−COO−、−OCO−、−C2F4−または−CF=CF−を表し、
pは、1または2を表し、および
vは、1〜6を表す。
Z3は、単結合、−CH2CH2−、−CH=CH−、−CF2O−、−OCF2−、−CH2O−、−OCH2−、−COO−、−OCO−、−C2F4−または−CF=CF−を表す。
alkylおよびalkyl*は、それぞれ互いに独立に、1〜6個の炭素原子を有する直鎖状のアルキル基を表す。
式IIAおよび/またはIIBの化合物の1種類以上を5〜80質量%
を含むか、またはそれらより成る液晶媒体(ただし、式IA、IB、IC、IDおよびIIAおよび/またはIIBの化合物の総量は、100質量%以下である。)。
R7およびR8は、それぞれ互いに独立に、前記式IIAおよびIIBのR2で示される意味の1つを有し、
wおよびxは、それぞれ互いに独立に、1〜6を表す。
mは1〜6を表す。
mは、1〜6を表す。
alkylおよびalkyl*は、それぞれ互いに独立に、1〜6個の炭素原子を有する直鎖状のアルキル基を表し、および
alkenylおよびalkenyl*は、それぞれ互いに独立に、2〜6個の炭素原子を有する直鎖状のアルケニル基を表す。
alkylおよびalkyl*は、それぞれ互いに独立に、1〜6個の炭素原子を有する直鎖状のアルキル基を表し、
alkenylおよびalkenyl*は、それぞれ互いに独立に、2〜6個の炭素原子を有する直鎖状のアルケニル基を表す。
式中、LおよびEは、それぞれ、1,4−二置換ベンゼンおよびシクロヘキサン環、4,4’−二置換ビフェニル、フェニルシクロヘキサンおよびシクロへキシルシクロヘキサン構造、2,5−二置換ピリミジンおよび1,3−ジオキサン環、2,6−二置換ナフタレン、ジ−およびテトラヒドロナフタレン、キナゾリンおよびテトラヒドロキナゾリンから成る群より選択される炭素環構造またはヘテロ環構造である。
V0は20℃における容量閾電圧(V)を表し、
Δnは20℃および589nmで測定される光学異方性を表し、
Δεは20℃および1kHzでの誘電異方性を表し、
cl.p.は透明点(℃)を表し、
K1は20℃における「スプレイ」変形に対する弾性定数(pN)を表し、
K3は20℃における「ベンド」変形に対する弾性定数(pN)を表し、
γ1は20℃で測定される回転粘度(mPa・s)を表し、磁場回転法で決定され、
LTSは試験セル中で決定される低温安定性(ネマチック相)を表し、
HR(20)は20℃における電圧保持率(%)を表し、
HR(100)は100℃における5分後の電圧保持率(%)を表し、
HR(UV)はUV曝露後の電圧保持率(%)を表す。
<例1>
Claims (10)
- 式IAの少なくとも1種類の化合物と、式IB、ICおよびIDから成る化合物群より選択される少なくとも1種類の化合物とを含み、
液晶媒体全体における式IAの化合物の割合が、15質量%以上である液晶媒体。
R1AおよびR1Bは、それぞれ互いに独立に、6個までの炭素原子を有するアルケニル基を表し、該基は置換されていないか、CNまたはCF3によって1置換されているか、またはハロゲンによって少なくとも1置換されており、ただし加えて、これらの基の中の1個以上のCH2基は、酸素原子が互いに直接結合しないようにして、−O−、−S−、
R2A、R2B、R1C、R1DおよびR2Dは、それぞれ互いに独立に、6個までの炭素原子を有するアルキルまたはアルケニル基を表し、該基は置換されていないか、CNまたはCF3によって1置換されているか、またはハロゲンによって少なくとも1置換されており、ただし加えて、これらの基の中の1個以上のCH2基は、酸素原子が互いに直接結合しないようにして、−O−、−S−、
ただし、式IBにおけるR1BおよびR2Bは置換されておらず、
Y4およびY5は、それぞれ互いに独立に、F、Cl、CF3、CHF2、CH2F、OCF3、OCH2F、OCHF2またはCNを表し、
Y3は、HまたはCH3を表し、
R2Cは、HまたはFを表し、
R3Cは、H、CH3、C2H5またはn−C3H7を表し、
aおよびbは、それぞれ互いに独立に、0、1または2を表し、ただしa+bは2であり、
cは、1または2を表し、および
dは、0または1を表す。) - 式IIAおよび/またはIIBの1種類以上の化合物を更に含む請求項1記載の液晶媒体。
R2は、H、または15個までの炭素原子を有するアルキルまたはアルケニル基を表し、該基は置換されていないか、CNまたはCF3によって1置換されているか、またはハロゲンによって少なくとも1置換されており、ただし加えて、これらの基の中の1個以上のCH2基は、酸素原子が互いに直接結合しないようにして、それぞれ互いに独立に、−O−、−S−、
L1〜4は、それぞれ互いに独立に、FまたはClを表し、
Z2は、単結合、−CH2CH2−、−CH=CH−、−CF2O−、−OCF2−、−CH2O−、−OCH2−、−COO−、−OCO−、−C2F4−または−CF=CF−を表し、
pは、1または2を表し、および
vは、1〜6を表す。) - 式IIAおよび/またはIIBの1種類以上の化合物を含む請求項1〜7のいずれか一項に記載の液晶媒体。
R2は、Hまたは15個までの炭素原子を有するアルキル基を表し、該基は置換されていないか、CNまたはCF3によって1置換されているか、またはハロゲンによって少なくとも1置換されており、ただし加えて、これらの基の中の1個以上のCH2基は、酸素原子が互いに直接結合しないようにして、−O−、−S−、
L1〜4は、それぞれ互いに独立に、FまたはClを表し、
Z2は、単結合、−CH2CH2−、−CH=CH−、−CF2O−、−OCF2−、−CH2O−、−OCH2−、−COO−、−OCO−、−C2F4−または−CF=CF−を表し、
pは、1または2を表し、および
vは、1〜6を表す。) - 式IAの少なくとも1種類の化合物を、式IB、ICおよびIDから成る化合物群より選択される少なくとも1種類の化合物、および任意成分として更なる液晶化合物および/または添加剤と混合することを特徴とする請求項1〜8のいずれか一項に記載の液晶媒体の調製方法。
- 誘電体として請求項1〜8のいずれか一項に記載の液晶媒体を含有することを特徴とする、ECB、PALC、FFSまたはIPS効果に基づくアクティブマトリクス駆動を有する電気光学的ディスプレイ。
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Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1977031B (zh) | 2004-07-02 | 2012-04-18 | 默克专利股份有限公司 | 液晶介质 |
EP1958999B1 (de) * | 2007-02-13 | 2012-07-11 | Merck Patent GmbH | Flüssigkristallines Medium |
DE602008003216D1 (de) * | 2007-05-16 | 2010-12-09 | Merck Patent Gmbh | Flüssigkristallines medium |
JP5566995B2 (ja) * | 2008-03-17 | 2014-08-06 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | 液晶媒体 |
TW201011096A (en) * | 2008-09-03 | 2010-03-16 | Au Optronics Corp | Vertical alignment liquid crystal display panel and liquid crystal material thereof |
US8206795B2 (en) * | 2008-09-09 | 2012-06-26 | Jnc Corporation | Liquid crystal composition and liquid crystal display device |
DE102008064171A1 (de) * | 2008-12-22 | 2010-07-01 | Merck Patent Gmbh | Flüssigkristallines Medium |
US20100315568A1 (en) * | 2009-06-16 | 2010-12-16 | Kent State University | Liquid crystal devices and methods providing fast switching mode |
CA3030271C (en) | 2009-10-08 | 2021-08-17 | Delos Living, Llc | Led lighting system |
DE102011009691A1 (de) * | 2010-02-09 | 2011-08-11 | Merck Patent GmbH, 64293 | Flüssigkristallines Medium |
CN102477305B (zh) * | 2010-11-25 | 2013-10-23 | 达兴材料股份有限公司 | 液晶化合物与液晶混合物 |
US9080101B2 (en) | 2010-12-24 | 2015-07-14 | Dic Corporation | Polymerizable compound-containing liquid crystal composition and liquid crystal display device using the same |
TW201333174A (zh) * | 2012-02-14 | 2013-08-16 | Jnc Corp | 液晶組成物及其用途、以及液晶顯示元件 |
CN104136576B (zh) * | 2012-02-22 | 2020-10-16 | 默克专利股份有限公司 | 液晶介质 |
US9593281B2 (en) * | 2012-07-04 | 2017-03-14 | Dic Corporation | Nematic liquid crystal composition and liquid crystal display device |
JP2015534701A (ja) | 2012-08-28 | 2015-12-03 | デロス リビング エルエルシーDelos Living Llc | 居住環境に関連するウェルネスを増進するためのシステム、方法、及び物品 |
TWI535828B (zh) | 2012-09-11 | 2016-06-01 | Dainippon Ink & Chemicals | A nematic liquid crystal composition, and a liquid crystal display device using the same |
DE102013017173A1 (de) | 2012-10-18 | 2014-04-24 | Merck Patent Gmbh | Flüssigkristallines Medium, Methode zu seiner Stabilisierung und Flüssigkristallanzeige |
KR102092042B1 (ko) | 2013-01-24 | 2020-03-24 | 삼성디스플레이 주식회사 | 액정 표시 장치 및 이의 제조 방법 |
CN105694910A (zh) * | 2013-03-26 | 2016-06-22 | Dic株式会社 | 液晶组合物以及使用其的液晶显示元件 |
CN105733609A (zh) * | 2013-03-26 | 2016-07-06 | Dic株式会社 | 液晶组合物以及使用其的液晶显示元件 |
WO2014203567A1 (ja) * | 2013-06-17 | 2014-12-24 | Dic株式会社 | ネマチック液晶組成物及びこれを用いた液晶表示素子 |
JP5729580B1 (ja) * | 2013-06-26 | 2015-06-03 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
WO2015034018A1 (ja) | 2013-09-06 | 2015-03-12 | Dic株式会社 | ネマチック液晶組成物及びこれを用いた液晶表示素子 |
EP3040398B1 (en) | 2013-10-08 | 2018-08-15 | DIC Corporation | Nematic liquid crystal composition and liquid crystal display element using same |
MX2016011107A (es) | 2014-02-28 | 2017-02-17 | Delos Living Llc | Sistemas, metodos y articulos para mejorar el bienestar asociado con ambientes habitables. |
KR20150109543A (ko) * | 2014-03-19 | 2015-10-02 | 삼성디스플레이 주식회사 | 액정 조성물 및 이를 포함하는 액정 표시 장치 |
JP5971448B2 (ja) | 2014-05-13 | 2016-08-17 | Dic株式会社 | ネマチック液晶組成物及びこれを用いた液晶表示素子 |
EP2990460B1 (de) * | 2014-08-22 | 2019-04-03 | Merck Patent GmbH | Flüssigkristallines medium |
DE102015013980A1 (de) | 2014-11-11 | 2016-05-12 | Merck Patent Gmbh | Heterocyclische Verbindung, Flüssigkristallines Medium, Methode zu seiner Stabilisierung und Fküssigkristallanzeige |
CN111849508A (zh) | 2014-12-25 | 2020-10-30 | Dic株式会社 | 向列液晶组合物及使用其的液晶显示元件 |
WO2016115230A1 (en) | 2015-01-13 | 2016-07-21 | Delos Living Llc | Systems, methods and articles for monitoring and enhancing human wellness |
WO2016136315A1 (ja) * | 2015-02-24 | 2016-09-01 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
KR102316210B1 (ko) * | 2015-03-06 | 2021-10-22 | 삼성디스플레이 주식회사 | 액정 조성물, 이를 포함하는 액정 표시 장치 |
KR20170079970A (ko) * | 2015-12-31 | 2017-07-10 | 주식회사 동진쎄미켐 | 액정 조성물 및 이를 포함하는 액정 표시 장치 |
KR20170088297A (ko) * | 2016-01-22 | 2017-08-01 | 주식회사 동진쎄미켐 | 액정 조성물 |
WO2017150056A1 (ja) * | 2016-02-29 | 2017-09-08 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
DE102017002925A1 (de) | 2016-04-21 | 2017-10-26 | Merck Patent Gmbh | Flüssigkristallines Medium |
JPWO2017195585A1 (ja) * | 2016-05-10 | 2018-05-24 | Dic株式会社 | 液晶表示素子 |
DE102017005884A1 (de) | 2016-07-07 | 2018-01-11 | Merck Patent Gmbh | Elektronisches Schaltelement |
KR102668909B1 (ko) | 2016-08-11 | 2024-05-24 | 티씨엘 차이나 스타 옵토일렉트로닉스 테크놀로지 컴퍼니 리미티드 | 액정 표시 장치 및 이에 포함되는 액정 조성물 |
US11338107B2 (en) | 2016-08-24 | 2022-05-24 | Delos Living Llc | Systems, methods and articles for enhancing wellness associated with habitable environments |
KR102639180B1 (ko) | 2016-08-25 | 2024-02-23 | 삼성디스플레이 주식회사 | 액정 표시 장치 및 이에 포함되는 액정 조성물 |
TW201833304A (zh) * | 2016-10-17 | 2018-09-16 | 德商馬克專利公司 | 液晶介質、液晶化合物及含彼之液晶顯示器 |
WO2019046580A1 (en) | 2017-08-30 | 2019-03-07 | Delos Living Llc | SYSTEMS, METHODS AND ARTICLES FOR EVALUATING AND / OR IMPROVING HEALTH AND WELL-BEING |
EP3850458A4 (en) | 2018-09-14 | 2022-06-08 | Delos Living, LLC | AIR CLEANING SYSTEMS AND PROCEDURES |
US11844163B2 (en) | 2019-02-26 | 2023-12-12 | Delos Living Llc | Method and apparatus for lighting in an office environment |
US11898898B2 (en) | 2019-03-25 | 2024-02-13 | Delos Living Llc | Systems and methods for acoustic monitoring |
CN114196420B (zh) * | 2020-09-17 | 2024-07-19 | 江苏和成显示科技有限公司 | 液晶组合物及其液晶显示器件 |
Family Cites Families (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE795849A (fr) | 1972-02-26 | 1973-08-23 | Merck Patent Gmbh | Phases nematiques modifiees |
US3814700A (en) | 1972-08-03 | 1974-06-04 | Ibm | Method for controllably varying the electrical properties of nematic liquids and dopants therefor |
DE2450088A1 (de) | 1974-10-22 | 1976-04-29 | Merck Patent Gmbh | Biphenylester |
DE2637430A1 (de) | 1976-08-20 | 1978-02-23 | Merck Patent Gmbh | Fluessigkristallines dielektrikum |
DE2853728A1 (de) | 1978-12-13 | 1980-07-17 | Merck Patent Gmbh | Fluessigkristalline carbonsaeureester, verfahren zu ihrer herstellung, diese enthaltende dielektrika und elektrooptisches anzeigeelement |
DE3465192D1 (en) * | 1983-03-16 | 1987-09-10 | Hoffmann La Roche | Liquid crystal components having an alkenyl chain |
EP0168683B1 (de) | 1984-07-16 | 1990-11-28 | F. Hoffmann-La Roche Ag | Flüssigkristalle mit Alkenyl- oder Alkenyloxygruppen |
FR2595157B1 (fr) | 1986-02-28 | 1988-04-29 | Commissariat Energie Atomique | Cellule a double couche de cristal liquide, utilisant l'effet de birefringence controlee electriquement et procede de fabrication d'un milieu uniaxe d'anisotropie optique negative utilisable dans cette cellule |
DE3906040A1 (de) | 1988-03-10 | 1989-09-21 | Merck Patent Gmbh | Cyclohexenderivate |
JP4320824B2 (ja) * | 1998-06-02 | 2009-08-26 | チッソ株式会社 | Δεが負の値を有するアルケニル化合物、液晶組成物および液晶表示素子 |
DE19927627B4 (de) | 1998-06-30 | 2008-01-31 | Merck Patent Gmbh | Flüssigkristallines Medium |
JP2001136669A (ja) * | 1999-11-01 | 2001-05-18 | Toyota Central Res & Dev Lab Inc | 蓄電装置 |
DE10107544A1 (de) * | 2000-03-24 | 2001-09-27 | Merck Patent Gmbh | Flüssigktistallmedium und dieses enthaltende elekrooptische Anzeige |
AU2001289901A1 (en) * | 2000-12-07 | 2002-06-18 | Merck Patent G.M.B.H | Liquid crystalline medium |
JP5279975B2 (ja) | 2000-12-19 | 2013-09-04 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | 負のdc異方性のアルケニル化合物と液晶性媒体 |
DE10064995B4 (de) * | 2000-12-23 | 2009-09-24 | Merck Patent Gmbh | Flüssigkristallines Medium und seine Verwendung in einer elektrooptischen Anzeige |
DE10218976A1 (de) * | 2001-06-01 | 2002-12-05 | Merck Patent Gmbh | Flüssigkristallines Medium |
DE10135499A1 (de) | 2001-07-20 | 2003-01-30 | Merck Patent Gmbh | Indanverbindungen mit negativem Delta-epsilon |
DE10204236A1 (de) | 2002-02-02 | 2003-08-07 | Merck Patent Gmbh | Verfahren zur Herstellung von Alkenen |
EP1378557B1 (de) | 2002-07-06 | 2007-02-21 | MERCK PATENT GmbH | Flüssigkristallines Medium |
KR101124758B1 (ko) * | 2002-11-22 | 2012-03-28 | 메르크 파텐트 게엠베하 | 액정 매질 |
JP4835021B2 (ja) * | 2004-04-09 | 2011-12-14 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
JP2005298733A (ja) * | 2004-04-14 | 2005-10-27 | Chisso Corp | 液晶組成物および液晶表示素子 |
CN1977031B (zh) * | 2004-07-02 | 2012-04-18 | 默克专利股份有限公司 | 液晶介质 |
JP4857552B2 (ja) * | 2004-12-06 | 2012-01-18 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
JP4876408B2 (ja) * | 2005-03-01 | 2012-02-15 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
EP1873134B1 (en) * | 2005-03-03 | 2013-02-13 | JNC Corporation | Chlorofluorobenzene liquid crystalline compound, liquid crystal composition, and liquid crystal display element |
EP2199362B1 (de) * | 2006-07-19 | 2012-08-29 | Merck Patent GmbH | Flüssigkristallines Medium |
US7803436B2 (en) * | 2006-08-07 | 2010-09-28 | Chisso Corporation | Liquid crystal composition and liquid crystal display device |
EP1958999B1 (de) * | 2007-02-13 | 2012-07-11 | Merck Patent GmbH | Flüssigkristallines Medium |
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TW201433626A (zh) | 2014-09-01 |
US20120228549A1 (en) | 2012-09-13 |
TW200848497A (en) | 2008-12-16 |
JP2008208365A (ja) | 2008-09-11 |
TW201439286A (zh) | 2014-10-16 |
US7767280B2 (en) | 2010-08-03 |
TW201704456A (zh) | 2017-02-01 |
TWI558798B (zh) | 2016-11-21 |
US20100102275A1 (en) | 2010-04-29 |
US7981487B2 (en) | 2011-07-19 |
TWI470061B (zh) | 2015-01-21 |
JP2013177594A (ja) | 2013-09-09 |
KR20080075789A (ko) | 2008-08-19 |
JP6054229B2 (ja) | 2016-12-27 |
JP6479740B2 (ja) | 2019-03-06 |
KR101496269B1 (ko) | 2015-02-26 |
TWI550073B (zh) | 2016-09-21 |
US8361568B2 (en) | 2013-01-29 |
DE102008006875A1 (de) | 2008-08-14 |
US8475889B2 (en) | 2013-07-02 |
JP2017052957A (ja) | 2017-03-16 |
KR101540185B1 (ko) | 2015-07-28 |
TWI618784B (zh) | 2018-03-21 |
TW201433627A (zh) | 2014-09-01 |
TWI558799B (zh) | 2016-11-21 |
EP1958999A1 (de) | 2008-08-20 |
KR20140119678A (ko) | 2014-10-10 |
US20080191167A1 (en) | 2008-08-14 |
EP1958999B1 (de) | 2012-07-11 |
US20100243958A1 (en) | 2010-09-30 |
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