KR101353139B1 - 액정 매질 - Google Patents
액정 매질 Download PDFInfo
- Publication number
- KR101353139B1 KR101353139B1 KR1020087005699A KR20087005699A KR101353139B1 KR 101353139 B1 KR101353139 B1 KR 101353139B1 KR 1020087005699 A KR1020087005699 A KR 1020087005699A KR 20087005699 A KR20087005699 A KR 20087005699A KR 101353139 B1 KR101353139 B1 KR 101353139B1
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- compound
- liquid crystal
- compounds
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 59
- 150000001875 compounds Chemical class 0.000 claims abstract description 109
- 239000000203 mixture Substances 0.000 claims abstract description 50
- 230000000694 effects Effects 0.000 claims abstract description 16
- 239000011159 matrix material Substances 0.000 claims abstract description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 25
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- 239000007788 liquid Substances 0.000 claims description 20
- 239000000126 substance Substances 0.000 claims description 18
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 2
- 150000001911 terphenyls Chemical class 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 4
- 230000000996 additive effect Effects 0.000 claims 1
- YCLAMANSVUJYPT-UHFFFAOYSA-L aluminum chloride hydroxide hydrate Chemical compound O.[OH-].[Al+3].[Cl-] YCLAMANSVUJYPT-UHFFFAOYSA-L 0.000 abstract description 3
- 210000004027 cell Anatomy 0.000 description 17
- -1 alkenyl radical Chemical class 0.000 description 13
- 0 *C(CC1)CCC1C(CC1)CCC1*=C Chemical compound *C(CC1)CCC1C(CC1)CCC1*=C 0.000 description 12
- 125000003342 alkenyl group Chemical group 0.000 description 12
- 230000004044 response Effects 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 8
- 125000003545 alkoxy group Chemical group 0.000 description 6
- 230000003287 optical effect Effects 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 239000004990 Smectic liquid crystal Substances 0.000 description 5
- 235000010290 biphenyl Nutrition 0.000 description 5
- 239000002019 doping agent Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 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 4
- 239000004988 Nematic liquid crystal Substances 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 150000004074 biphenyls Chemical class 0.000 description 4
- 150000002367 halogens Chemical group 0.000 description 4
- 150000003254 radicals 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
- 230000008859 change Effects 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 125000003302 alkenyloxy group Chemical group 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical compound C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 2
- WVIIMZNLDWSIRH-UHFFFAOYSA-N cyclohexylcyclohexane Chemical compound C1CCCCC1C1CCCCC1 WVIIMZNLDWSIRH-UHFFFAOYSA-N 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- PKORYTIUMAOPED-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinazoline Chemical class C1=CC=C2NCNCC2=C1 PKORYTIUMAOPED-UHFFFAOYSA-N 0.000 description 1
- GRZJZRHVJAXMRR-UHFFFAOYSA-N 1-cyclohexyl-2-phenylbenzene Chemical group C1CCCCC1C1=CC=CC=C1C1=CC=CC=C1 GRZJZRHVJAXMRR-UHFFFAOYSA-N 0.000 description 1
- RAYZALBEMJMGEA-UHFFFAOYSA-N 1-cyclohexylnaphthalene Chemical compound C1CCCCC1C1=CC=CC2=CC=CC=C12 RAYZALBEMJMGEA-UHFFFAOYSA-N 0.000 description 1
- GVQIKUVVJFKEDH-UHFFFAOYSA-N 2,5-dicyclohexyl-5-phenylcyclohexa-1,3-diene Chemical group C1(CCCCC1)C1(CC=C(C=C1)C1CCCCC1)C1=CC=CC=C1 GVQIKUVVJFKEDH-UHFFFAOYSA-N 0.000 description 1
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- SMHSPYVJAUGNOI-UHFFFAOYSA-N 2-cyclohexyl-1,4-dioxane Chemical compound C1CCCCC1C1OCCOC1 SMHSPYVJAUGNOI-UHFFFAOYSA-N 0.000 description 1
- YJDDXMSIMBMMGY-UHFFFAOYSA-N 2-cyclohexylpyrimidine Chemical compound C1CCCCC1C1=NC=CC=N1 YJDDXMSIMBMMGY-UHFFFAOYSA-N 0.000 description 1
- WLNDDIWESXCXHM-UHFFFAOYSA-N 2-phenyl-1,4-dioxane Chemical group C1OCCOC1C1=CC=CC=C1 WLNDDIWESXCXHM-UHFFFAOYSA-N 0.000 description 1
- YKMVAIHFVHSSPH-UHFFFAOYSA-N Cc(cc1)ccc1-c(ccc(O)c1F)c1F Chemical compound Cc(cc1)ccc1-c(ccc(O)c1F)c1F YKMVAIHFVHSSPH-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- 229940123457 Free radical scavenger Drugs 0.000 description 1
- YCVUBQMQBSGECY-UHFFFAOYSA-N Nc(c(O)ccc1ON)c1N Chemical compound Nc(c(O)ccc1ON)c1N YCVUBQMQBSGECY-UHFFFAOYSA-N 0.000 description 1
- 102100038239 Protein Churchill Human genes 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
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000004423 acyloxy group Chemical group 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
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- JRXXLCKWQFKACW-UHFFFAOYSA-N biphenylacetylene Chemical compound C1=CC=CC=C1C#CC1=CC=CC=C1 JRXXLCKWQFKACW-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 1
- 150000001851 cinnamic acid derivatives Chemical class 0.000 description 1
- 238000007796 conventional method Methods 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 compound C=1C=CC=CC=1C(=O)OC1CCCCC1 DQZKGSRJOUYVPL-UHFFFAOYSA-N 0.000 description 1
- VJCWGXGMXAVKJU-UHFFFAOYSA-N cyclohexyl cyclohexanecarboxylate Chemical compound C1CCCCC1C(=O)OC1CCCCC1 VJCWGXGMXAVKJU-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
- 230000007423 decrease Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 125000000532 dioxanyl group Chemical group 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
- 238000010438 heat treatment 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
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 230000001795 light effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QLNWXBAGRTUKKI-UHFFFAOYSA-N metacetamol Chemical compound CC(=O)NC1=CC=CC(O)=C1 QLNWXBAGRTUKKI-UHFFFAOYSA-N 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
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 1
- UVEWQKMPXAHFST-UHFFFAOYSA-N n,1-diphenylmethanimine Chemical compound 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
- 239000003960 organic solvent Substances 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
- BOTNYLSAWDQNEX-UHFFFAOYSA-N phenoxymethylbenzene Chemical compound C=1C=CC=CC=1COC1=CC=CC=C1 BOTNYLSAWDQNEX-UHFFFAOYSA-N 0.000 description 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 1
- 125000002294 quinazolinyl group Chemical class N1=C(N=CC2=CC=CC=C12)* 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
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical class C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- 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)
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- 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
- C09K19/34—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- 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
- C09K2019/0444—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Liquid Crystal Substances (AREA)
- Liquid Crystal (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005048064 | 2005-08-09 | ||
| DE102005048064.0 | 2005-08-09 | ||
| PCT/EP2006/007692 WO2007017180A1 (de) | 2005-08-09 | 2006-08-03 | Flüssigkristallines medium |
Related Child Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020137030544A Division KR101432959B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
| KR1020137030541A Division KR101496268B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
| KR1020137010690A Division KR101468828B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20080030693A KR20080030693A (ko) | 2008-04-04 |
| KR101353139B1 true KR101353139B1 (ko) | 2014-01-17 |
Family
ID=37081005
Family Applications (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020087005699A Active KR101353139B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
| KR1020137030541A Active KR101496268B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
| KR1020147026303A Active KR101540195B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
| KR1020137030544A Active KR101432959B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
| KR1020137010690A Active KR101468828B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
Family Applications After (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020137030541A Active KR101496268B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
| KR1020147026303A Active KR101540195B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
| KR1020137030544A Active KR101432959B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
| KR1020137010690A Active KR101468828B1 (ko) | 2005-08-09 | 2006-08-03 | 액정 매질 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US8025935B2 (https=) |
| EP (1) | EP1913114B1 (https=) |
| JP (5) | JP5512124B2 (https=) |
| KR (5) | KR101353139B1 (https=) |
| CN (3) | CN103382392B (https=) |
| AT (1) | ATE501231T1 (https=) |
| DE (1) | DE502006009061D1 (https=) |
| TW (1) | TWI437079B (https=) |
| WO (1) | WO2007017180A1 (https=) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5259185B2 (ja) | 2004-07-02 | 2013-08-07 | 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 |
| ATE437211T1 (de) * | 2005-05-21 | 2009-08-15 | Merck Patent Gmbh | Flüssigkristallines medium |
| WO2009121458A1 (de) * | 2008-03-31 | 2009-10-08 | Merck Patent Gmbh | Flüssigkristallines medium und flüssigkristallanzeige |
| EP3075816B1 (en) | 2009-01-22 | 2018-05-23 | JNC Corporation | Liquid crystal composition and liquid crystal display device |
| US9914877B2 (en) * | 2010-12-07 | 2018-03-13 | Merck Patent Gmbh | Liquid crystal medium and liquid crystal display |
| JP5196073B2 (ja) | 2010-12-24 | 2013-05-15 | Ｄｉｃ株式会社 | 重合性化合物含有液晶組成物及びそれを使用した液晶表示素子 |
| CN103748325B (zh) | 2011-04-05 | 2017-03-15 | 卡明斯散发控制技术公司 | 用于后处理系统监测的系统、方法和设备 |
| CN102433130B (zh) * | 2011-09-23 | 2014-03-19 | 北京八亿时空液晶科技股份有限公司 | 一种负介电各向异性液晶组合物及其应用 |
| EP2818532A4 (en) * | 2012-02-23 | 2016-11-09 | Jnc Corp | LIQUID CRYSTAL COMPOSITION AND LIQUID CRYSTAL DISPLAY ELEMENT |
| TWI452122B (zh) | 2012-02-24 | 2014-09-11 | Dainippon Ink & Chemicals | 液晶組成物 |
| JP5585745B1 (ja) | 2013-03-06 | 2014-09-10 | 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 |
| KR102150931B1 (ko) | 2013-03-26 | 2020-09-02 | 디아이씨 가부시끼가이샤 | 액정 조성물 및 그것을 사용한 액정 표시 소자 |
| KR102068961B1 (ko) | 2013-06-28 | 2020-01-22 | 엘지디스플레이 주식회사 | 액정 물질 및 이를 포함하는 액정표시장치 |
| EP2896678B1 (en) * | 2014-01-21 | 2018-10-17 | Merck Patent GmbH | Liquid crystal display |
| WO2015122458A1 (ja) * | 2014-02-14 | 2015-08-20 | Dic株式会社 | 光変調素子 |
| JP7086914B2 (ja) * | 2014-03-17 | 2022-06-20 | 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 |
| CN103923663B (zh) * | 2014-04-15 | 2015-09-23 | 烟台显华化工科技有限公司 | 一种负介电各向异性液晶材料及使用该材料的显示器件 |
| US10351772B2 (en) | 2014-05-13 | 2019-07-16 | Dic Corporation | Nematic liquid crystal composition and liquid crystal display element using same |
| JP2017517606A (ja) * | 2014-05-27 | 2017-06-29 | 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Ｍｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ | 液晶媒体 |
| JP5950061B2 (ja) * | 2014-07-25 | 2016-07-13 | Dic株式会社 | 液晶組成物及びそれを使用した液晶表示素子 |
| WO2016035786A1 (ja) | 2014-09-05 | 2016-03-10 | 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 |
| KR20160035173A (ko) | 2014-09-22 | 2016-03-31 | 삼성디스플레이 주식회사 | 액정 화합물, 이를 포함하는 액정 조성물 및 이를 포함하는 액정 디스플레이 |
| JP2016079292A (ja) * | 2014-10-17 | 2016-05-16 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
| WO2016104165A1 (ja) | 2014-12-25 | 2016-06-30 | 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 |
| US20160264866A1 (en) * | 2015-03-10 | 2016-09-15 | Merck Patent Gmbh | Liquid-crystalline medium |
| EP3067405B1 (de) * | 2015-03-10 | 2019-03-27 | Merck Patent GmbH | Flüssigkristallines medium |
| US20170362506A1 (en) | 2015-03-13 | 2017-12-21 | Merck Patent Gmbh | Liquid-crystalline medium |
| KR20160122074A (ko) * | 2015-04-13 | 2016-10-21 | 메르크 파텐트 게엠베하 | 액정 매질 및 이를 포함하는 액정 디스플레이 |
| JP6308412B2 (ja) * | 2015-07-01 | 2018-04-11 | Dic株式会社 | 組成物およびそれを使用した液晶表示素子 |
| CN105694909B (zh) * | 2016-01-13 | 2018-08-28 | 石家庄诚志永华显示材料有限公司 | 液晶组合物 |
| CN107267157B (zh) * | 2016-04-08 | 2020-07-31 | 北京八亿时空液晶科技股份有限公司 | 一种负介电各向异性液晶组合物及其应用 |
| JP2017193596A (ja) * | 2016-04-18 | 2017-10-26 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
| WO2019135350A1 (ja) * | 2018-01-05 | 2019-07-11 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
| JP7124462B2 (ja) * | 2018-05-31 | 2022-08-24 | Jnc株式会社 | 液晶表示素子 |
| WO2020152206A1 (en) | 2019-01-25 | 2020-07-30 | Merck Patent Gmbh | Liquid-crystalline medium |
| CN111484475B (zh) * | 2019-01-28 | 2022-11-04 | 北京八亿时空液晶科技股份有限公司 | 一种液晶化合物及其制备方法与应用 |
| KR102859499B1 (ko) * | 2020-02-21 | 2025-09-15 | 삼성디스플레이 주식회사 | 액정 조성물 및 이를 포함하는 표시 장치 |
| WO2021233797A1 (en) | 2020-05-18 | 2021-11-25 | Merck Patent Gmbh | Liquid-crystalline medium |
| EP3940040B1 (en) | 2020-07-16 | 2024-10-16 | Merck Patent GmbH | Liquid-crystalline medium |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998013321A1 (en) | 1996-09-27 | 1998-04-02 | Chisso Corporation | Compound having alkadienyl group as side chain, and liquid crystal composition using same |
| EP0834491A1 (de) * | 1996-10-02 | 1998-04-08 | MERCK PATENT GmbH | Bisalkenylbicyclohexane und flüssigkristallines Medium |
| JP2003183656A (ja) * | 2001-10-12 | 2003-07-03 | Merck Patent Gmbh | 液晶媒体 |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19732502A1 (de) * | 1997-07-29 | 1999-02-04 | Merck Patent Gmbh | STN-Flüssigkristallanzeige |
| DE19733199A1 (de) * | 1997-08-01 | 1999-02-04 | Merck Patent Gmbh | Nematische Flüssigkristallzusammensetzung |
| DE19927627B4 (de) * | 1998-06-30 | 2008-01-31 | Merck Patent Gmbh | Flüssigkristallines Medium |
| JP2000096055A (ja) * | 1998-09-12 | 2000-04-04 | Merck Patent Gmbh | ネマティック液晶組成物およびこの組成物を含有する液晶ディスプレイ |
| DE10058664B4 (de) | 1999-12-07 | 2009-12-03 | Merck Patent Gmbh | Flüssigkristallines Medium und seine Verwendung |
| DE10112955B4 (de) * | 2000-04-14 | 2010-09-09 | Merck Patent Gmbh | Flüssigkristallines Medium und seine Verwendung |
| 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 |
| DE10216197B4 (de) * | 2002-04-12 | 2013-02-07 | Merck Patent Gmbh | Flüssigkristallmedium und und seine Verwendung in einer elektrooptischen Anzeige |
| ATE354623T1 (de) * | 2002-07-06 | 2007-03-15 | Merck Patent Gmbh | Flüssigkristallines medium |
| EP1563035B1 (de) | 2002-11-22 | 2007-09-12 | MERCK PATENT GmbH | Flüssigkristallines medium |
| WO2004058917A1 (ja) * | 2002-12-26 | 2004-07-15 | Dainippon Ink And Chemicals, Inc. | ネマチック液晶組成物及びこれを用いた液晶表示素子 |
| JP4834954B2 (ja) * | 2002-12-26 | 2011-12-14 | 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 |
| DE102004003508B4 (de) * | 2003-02-15 | 2012-11-15 | Merck Patent Gmbh | Nematische Flüssigkristallmischung und ihre Verwendung in Anzeigen |
| EP1646703B1 (de) * | 2003-07-11 | 2010-03-17 | MERCK PATENT GmbH | Flüssigkristallines medium mit monofluor-terphenylverbindungen |
| DE102004039276B4 (de) * | 2003-09-19 | 2013-03-07 | Merck Patent Gmbh | Nematische Flüssigkristallmischung und deren Verwendung in Anzeigen |
| KR100716969B1 (ko) * | 2003-11-27 | 2007-05-10 | 삼성전자주식회사 | 수직 배향 액정화합물 및 이를 포함한 액정 조성물 |
| JP5259185B2 (ja) * | 2004-07-02 | 2013-08-07 | 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 |
| CN1989225B (zh) * | 2004-07-02 | 2012-07-11 | 默克专利股份有限公司 | 液晶介质和包含该液晶介质的电光学显示器 |
| DE502006002167D1 (de) * | 2005-08-09 | 2009-01-08 | Merck Patent Gmbh | Flüssigkristallines Medium |
| DE102005058541A1 (de) * | 2005-12-08 | 2007-06-14 | Merck Patent Gmbh | Flüssigkristallines Medium |
| DE502007004313D1 (de) * | 2007-02-19 | 2010-08-19 | Merck Patent Gmbh | Flüssigkristallines Medium |
| DE102008035890B4 (de) * | 2007-08-30 | 2017-10-19 | Merck Patent Gmbh | Flüssigkristallines Medium und seine Verwendung |
-
2006
- 2006-08-03 US US12/063,336 patent/US8025935B2/en active Active
- 2006-08-03 CN CN201310148910.XA patent/CN103382392B/zh active Active
- 2006-08-03 KR KR1020087005699A patent/KR101353139B1/ko active Active
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- 2006-08-03 EP EP06762965A patent/EP1913114B1/de active Active
- 2006-08-03 KR KR1020147026303A patent/KR101540195B1/ko active Active
- 2006-08-03 KR KR1020137030544A patent/KR101432959B1/ko active Active
- 2006-08-03 AT AT06762965T patent/ATE501231T1/de active
- 2006-08-03 KR KR1020137010690A patent/KR101468828B1/ko active Active
- 2006-08-03 WO PCT/EP2006/007692 patent/WO2007017180A1/de not_active Ceased
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- 2013-08-07 JP JP2013163786A patent/JP5893590B2/ja active Active
- 2013-08-07 JP JP2013163787A patent/JP5933493B2/ja active Active
-
2015
- 2015-12-25 JP JP2015252770A patent/JP6117328B2/ja active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998013321A1 (en) | 1996-09-27 | 1998-04-02 | Chisso Corporation | Compound having alkadienyl group as side chain, and liquid crystal composition using same |
| EP0834491A1 (de) * | 1996-10-02 | 1998-04-08 | MERCK PATENT GmbH | Bisalkenylbicyclohexane und flüssigkristallines Medium |
| JP2003183656A (ja) * | 2001-10-12 | 2003-07-03 | Merck Patent Gmbh | 液晶媒体 |
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