NO865304L - Smektiske flytende krystallinske faser. - Google Patents
Smektiske flytende krystallinske faser.Info
- Publication number
- NO865304L NO865304L NO865304A NO865304A NO865304L NO 865304 L NO865304 L NO 865304L NO 865304 A NO865304 A NO 865304A NO 865304 A NO865304 A NO 865304A NO 865304 L NO865304 L NO 865304L
- Authority
- NO
- Norway
- Prior art keywords
- heptylpyrimidine
- liquid
- octylpyrimidine
- trans
- formula
- Prior art date
Links
- 239000007788 liquid Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 71
- 239000004990 Smectic liquid crystal Substances 0.000 claims abstract description 24
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 22
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 18
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims abstract description 11
- 125000005407 trans-1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])[C@]([H])([*:2])C([H])([H])C([H])([H])[C@@]1([H])[*:1] 0.000 claims abstract description 8
- -1 4,4'-biphenylyl Chemical group 0.000 claims description 27
- 230000001747 exhibiting effect Effects 0.000 claims description 3
- 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 claims description 2
- 239000012071 phase Substances 0.000 description 108
- 239000000203 mixture Substances 0.000 description 20
- 230000002269 spontaneous effect Effects 0.000 description 20
- 230000010287 polarization Effects 0.000 description 15
- 238000007792 addition Methods 0.000 description 10
- 125000003545 alkoxy group Chemical group 0.000 description 10
- 239000002019 doping agent Substances 0.000 description 9
- 230000007704 transition Effects 0.000 description 9
- RVLAXPQGTRTHEV-UHFFFAOYSA-N 4-pentylcyclohexane-1-carboxylic acid Chemical compound CCCCCC1CCC(C(O)=O)CC1 RVLAXPQGTRTHEV-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 230000002349 favourable effect Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ANCNJBZIUJNIIY-UHFFFAOYSA-N 3-methyl-1-[2-[4-(4-pentylphenyl)phenyl]ethyl]cyclohexane-1-carbonitrile Chemical compound C1=CC(CCCCC)=CC=C1C(C=C1)=CC=C1CCC1(C#N)CC(C)CCC1 ANCNJBZIUJNIIY-UHFFFAOYSA-N 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- GRKYDVCWZVLSFH-UHFFFAOYSA-N ethyl 2-[4-(5-nonylpyrimidin-2-yl)phenoxy]propanoate Chemical compound N1=CC(CCCCCCCCC)=CN=C1C1=CC=C(OC(C)C(=O)OCC)C=C1 GRKYDVCWZVLSFH-UHFFFAOYSA-N 0.000 description 3
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- JAJUZYCJBSCIHW-LJQANCHMSA-N (2R)-2-chloro-2-[4-(5-hexylpyrimidin-2-yl)phenyl]propanoic acid Chemical compound N1=CC(CCCCCC)=CN=C1C1=CC=C([C@@](C)(Cl)C(O)=O)C=C1 JAJUZYCJBSCIHW-LJQANCHMSA-N 0.000 description 2
- HBQUXMZZODHFMJ-UHFFFAOYSA-N 4-hexoxybenzoic acid Chemical compound CCCCCCOC1=CC=C(C(O)=O)C=C1 HBQUXMZZODHFMJ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 125000004423 acyloxy group Chemical group 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- WVIIMZNLDWSIRH-UHFFFAOYSA-N cyclohexylcyclohexane Chemical group C1CCCCC1C1CCCCC1 WVIIMZNLDWSIRH-UHFFFAOYSA-N 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 125000006608 n-octyloxy group Chemical group 0.000 description 2
- 125000002560 nitrile group Chemical group 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- PJDWNSYGMXODTB-UHFFFAOYSA-N 1,2,3,4,4a,4b,5,6-octahydrophenanthrene Chemical compound C1=CCCC2C(CCCC3)C3=CC=C21 PJDWNSYGMXODTB-UHFFFAOYSA-N 0.000 description 1
- UXNCDAQNSQBHEN-UHFFFAOYSA-N 1,2,3,4-tetrahydrophenanthrene Chemical compound C1=CC2=CC=CC=C2C2=C1CCCC2 UXNCDAQNSQBHEN-UHFFFAOYSA-N 0.000 description 1
- 125000004955 1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C1([H])[*:2] 0.000 description 1
- OHVLMTFVQDZYHP-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CN1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O OHVLMTFVQDZYHP-UHFFFAOYSA-N 0.000 description 1
- KRPRTHCKGYISTE-UHFFFAOYSA-N 1-[4-(5-hexylpyridin-2-yl)phenyl]heptan-1-one Chemical compound C1=CC(C(=O)CCCCCC)=CC=C1C1=CC=C(CCCCCC)C=N1 KRPRTHCKGYISTE-UHFFFAOYSA-N 0.000 description 1
- 125000004959 2,6-naphthylene group Chemical group [H]C1=C([H])C2=C([H])C([*:1])=C([H])C([H])=C2C([H])=C1[*:2] 0.000 description 1
- VUUCNJSEDOSVDW-UHFFFAOYSA-N 2-[2-(4-heptoxyphenyl)ethyl]-5-heptylpyridine Chemical compound C1=CC(OCCCCCCC)=CC=C1CCC1=CC=C(CCCCCCC)C=N1 VUUCNJSEDOSVDW-UHFFFAOYSA-N 0.000 description 1
- DSKLUULPJLSLFG-UHFFFAOYSA-N 2-[2-(4-nonoxyphenyl)ethyl]-5-nonylpyridine Chemical compound C1=CC(OCCCCCCCCC)=CC=C1CCC1=CC=C(CCCCCCCCC)C=N1 DSKLUULPJLSLFG-UHFFFAOYSA-N 0.000 description 1
- ZAPGEVOELCSRJM-UHFFFAOYSA-N 2-[4-(4-heptoxyphenyl)phenyl]-5-heptylpyridine Chemical compound C1=CC(OCCCCCCC)=CC=C1C1=CC=C(C=2N=CC(CCCCCCC)=CC=2)C=C1 ZAPGEVOELCSRJM-UHFFFAOYSA-N 0.000 description 1
- ZZMUWFHWKSGUKF-UHFFFAOYSA-N 2-[4-(4-heptoxyphenyl)phenyl]-5-heptylpyrimidine Chemical compound C1=CC(OCCCCCCC)=CC=C1C1=CC=C(C=2N=CC(CCCCCCC)=CN=2)C=C1 ZZMUWFHWKSGUKF-UHFFFAOYSA-N 0.000 description 1
- ISTZZVNVJLERPL-UHFFFAOYSA-N 2-[4-(4-nonoxyphenyl)phenyl]-5-nonylpyridine Chemical compound C1=CC(OCCCCCCCCC)=CC=C1C1=CC=C(C=2N=CC(CCCCCCCCC)=CC=2)C=C1 ISTZZVNVJLERPL-UHFFFAOYSA-N 0.000 description 1
- WLPATYNQCGVFFH-UHFFFAOYSA-N 2-phenylbenzonitrile Chemical group N#CC1=CC=CC=C1C1=CC=CC=C1 WLPATYNQCGVFFH-UHFFFAOYSA-N 0.000 description 1
- COAYECRLEWBCAA-UHFFFAOYSA-N 3-(4-heptoxyphenyl)-6-heptylpyridazine Chemical compound C1=CC(OCCCCCCC)=CC=C1C1=CC=C(CCCCCCC)N=N1 COAYECRLEWBCAA-UHFFFAOYSA-N 0.000 description 1
- VDIYJVWLUCANFY-UHFFFAOYSA-N 3-(4-heptoxyphenyl)-6-hexylpyridazine Chemical compound C1=CC(OCCCCCCC)=CC=C1C1=CC=C(CCCCCC)N=N1 VDIYJVWLUCANFY-UHFFFAOYSA-N 0.000 description 1
- PWQBSYHSMGFPKN-UHFFFAOYSA-N 3-(4-heptoxyphenyl)pyridine Chemical compound C1=CC(OCCCCCCC)=CC=C1C1=CC=CN=C1 PWQBSYHSMGFPKN-UHFFFAOYSA-N 0.000 description 1
- NYPYPOZNGOXYSU-UHFFFAOYSA-N 3-bromopyridine Chemical compound BrC1=CC=CN=C1 NYPYPOZNGOXYSU-UHFFFAOYSA-N 0.000 description 1
- MLCNUFAMJKPRHB-UHFFFAOYSA-N 3-heptyl-6-(4-nonoxyphenyl)pyridazine Chemical compound C1=CC(OCCCCCCCCC)=CC=C1C1=CC=C(CCCCCCC)N=N1 MLCNUFAMJKPRHB-UHFFFAOYSA-N 0.000 description 1
- ZRVIYEJYXIDATJ-UHFFFAOYSA-N 4-Heptyloxybenzoic acid Chemical compound CCCCCCCOC1=CC=C(C(O)=O)C=C1 ZRVIYEJYXIDATJ-UHFFFAOYSA-N 0.000 description 1
- CCLVGHDFLATNLC-UHFFFAOYSA-N 4-[4-(2-methylbutyl)phenyl]benzoic acid Chemical compound C1=CC(CC(C)CC)=CC=C1C1=CC=C(C(O)=O)C=C1 CCLVGHDFLATNLC-UHFFFAOYSA-N 0.000 description 1
- OZGCLSHAAJYRFI-UHFFFAOYSA-N 4-bromoheptoxybenzene Chemical compound CCCC(Br)CCCOC1=CC=CC=C1 OZGCLSHAAJYRFI-UHFFFAOYSA-N 0.000 description 1
- JMAUQQIVJIRNDQ-UHFFFAOYSA-N 4-heptylcyclohexane-1-carboxylic acid Chemical compound CCCCCCCC1CCC(C(O)=O)CC1 JMAUQQIVJIRNDQ-UHFFFAOYSA-N 0.000 description 1
- KCMMQMJYXDZFEO-UHFFFAOYSA-N 5-heptyl-2-[2-(4-nonoxyphenyl)ethyl]pyridine Chemical compound C1=CC(OCCCCCCCCC)=CC=C1CCC1=CC=C(CCCCCCC)C=N1 KCMMQMJYXDZFEO-UHFFFAOYSA-N 0.000 description 1
- OJZHMNGDKHHWLO-UHFFFAOYSA-N 5-heptyl-2-[4-(4-octoxyphenyl)phenyl]pyrimidine Chemical compound C1=CC(OCCCCCCCC)=CC=C1C1=CC=C(C=2N=CC(CCCCCCC)=CN=2)C=C1 OJZHMNGDKHHWLO-UHFFFAOYSA-N 0.000 description 1
- GGBJHURWWWLEQH-UHFFFAOYSA-N Butyl-cyclohexane Natural products CCCCC1CCCCC1 GGBJHURWWWLEQH-UHFFFAOYSA-N 0.000 description 1
- BRVPBLGSWREYSP-BUKAYNEZSA-N C(#N)C(C[C@@H]1CC[C@H](CC1)CCC)[C@@H]1CC[C@H](CC1)CCCCC Chemical compound C(#N)C(C[C@@H]1CC[C@H](CC1)CCC)[C@@H]1CC[C@H](CC1)CCCCC BRVPBLGSWREYSP-BUKAYNEZSA-N 0.000 description 1
- ISBOLLOFPIFMFT-IBBUNRCRSA-N C(#N)C(C[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCCCC)[C@@H]1CC[C@H](CC1)CCCCC Chemical compound C(#N)C(C[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCCCC)[C@@H]1CC[C@H](CC1)CCCCC ISBOLLOFPIFMFT-IBBUNRCRSA-N 0.000 description 1
- LOBBOIDWTIMNHR-CHDDOINTSA-N C(CCCC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)OC(CCCCC)=O Chemical compound C(CCCC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)OC(CCCCC)=O LOBBOIDWTIMNHR-CHDDOINTSA-N 0.000 description 1
- IHQRYZMWUVQQPY-SOAUALDESA-N C(CCCCCC)[C@@H]1CC[C@H](CC1)CCC1=NC=C(C=C1)OCCCCCCC Chemical compound C(CCCCCC)[C@@H]1CC[C@H](CC1)CCC1=NC=C(C=C1)OCCCCCCC IHQRYZMWUVQQPY-SOAUALDESA-N 0.000 description 1
- JUNLOFBLASUAIJ-DIVCQZSQSA-N C(CCCCCC)[C@@H]1CC[C@H](CC1)CCC1=NC=C(C=C1)OCCCCCCCC Chemical compound C(CCCCCC)[C@@H]1CC[C@H](CC1)CCC1=NC=C(C=C1)OCCCCCCCC JUNLOFBLASUAIJ-DIVCQZSQSA-N 0.000 description 1
- RGUPLOJZCIDSNS-MCZWQBSQSA-N C(CCCCCC)[C@@H]1CC[C@H](CC1)CCC1=NC=C(C=C1)OCCCCCCCCC Chemical compound C(CCCCCC)[C@@H]1CC[C@H](CC1)CCC1=NC=C(C=C1)OCCCCCCCCC RGUPLOJZCIDSNS-MCZWQBSQSA-N 0.000 description 1
- DZJUEYNFTBEVFZ-UHFFFAOYSA-N CCCCCCCCCC1=CN=C(C(O)=O)C(C=2C=CC=CC=2)=C1OCCCCCCCC Chemical compound CCCCCCCCCC1=CN=C(C(O)=O)C(C=2C=CC=CC=2)=C1OCCCCCCCC DZJUEYNFTBEVFZ-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004988 Nematic liquid crystal Substances 0.000 description 1
- MTZJEPNYXNJVNI-UHFFFAOYSA-M [Br-].CCCCCCCOC1=CC=C([Mg+])C=C1 Chemical compound [Br-].CCCCCCCOC1=CC=C([Mg+])C=C1 MTZJEPNYXNJVNI-UHFFFAOYSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000001589 carboacyl group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000006610 n-decyloxy group Chemical group 0.000 description 1
- 125000006609 n-nonyloxy group Chemical group 0.000 description 1
- QVCSVYXORSWDJF-UHFFFAOYSA-N octan-2-yl 4-[[4-(5-nonylpyrimidin-2-yl)phenoxy]methyl]benzoate Chemical compound N1=CC(CCCCCCCCC)=CN=C1C(C=C1)=CC=C1OCC1=CC=C(C(=O)OC(C)CCCCCC)C=C1 QVCSVYXORSWDJF-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000001931 thermography Methods 0.000 description 1
- 230000009466 transformation Effects 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
- C09K19/34—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
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/34—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
- C09K19/3441—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other 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
- C09K19/34—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
- C09K19/3441—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom
- C09K19/345—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom the heterocyclic ring being a six-membered aromatic ring containing two nitrogen atoms
-
- 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
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Liquid Crystal Substances (AREA)
- Liquid Crystal (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Dental Preparations (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Polarising Elements (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3515374A DE3515374C2 (de) | 1985-04-27 | 1985-04-27 | Chirale getilte smektische flüssigkristalline Phasen und deren Verwendung in elektrooptischen Anzeigeelementen |
| PCT/EP1986/000234 WO1986006401A1 (en) | 1985-04-27 | 1986-04-19 | Smectic liquid crystalline phases |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO865304D0 NO865304D0 (no) | 1986-12-23 |
| NO865304L true NO865304L (no) | 1987-02-09 |
Family
ID=6269372
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO865304A NO865304L (no) | 1985-04-27 | 1986-12-23 | Smektiske flytende krystallinske faser. |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US5064566A (ko) |
| EP (1) | EP0220296B1 (ko) |
| JP (1) | JPS62502624A (ko) |
| KR (1) | KR940005838B1 (ko) |
| AT (1) | ATE92091T1 (ko) |
| AU (1) | AU586687B2 (ko) |
| BR (1) | BR8606648A (ko) |
| CA (1) | CA1272017A (ko) |
| DD (1) | DD257444A5 (ko) |
| DE (2) | DE3515374C2 (ko) |
| DK (1) | DK629686D0 (ko) |
| FI (1) | FI865270A (ko) |
| NO (1) | NO865304L (ko) |
| WO (1) | WO1986006401A1 (ko) |
Families Citing this family (62)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0191860B1 (en) * | 1984-06-07 | 1990-04-18 | Seiko Instruments Inc. | Liquid crystal compound |
| EP0178647B1 (en) * | 1984-10-18 | 1993-09-29 | Chisso Corporation | Ferroelectric chiral smectic liquid crystal composition |
| US4721367A (en) * | 1985-04-01 | 1988-01-26 | Canon Kabushiki Kaisha | Liquid crystal device |
| DE3515373A1 (de) * | 1985-04-27 | 1986-11-06 | Merck Patent Gmbh, 6100 Darmstadt | Stickstoffhaltige heterocyclen |
| US4874546A (en) * | 1985-05-15 | 1989-10-17 | Chisso Corporation | Phenylpyrimidinecarboxylate derivative |
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-
1985
- 1985-04-27 DE DE3515374A patent/DE3515374C2/de not_active Expired - Fee Related
-
1986
- 1986-04-19 EP EP86903293A patent/EP0220296B1/de not_active Expired - Lifetime
- 1986-04-19 BR BR8606648A patent/BR8606648A/pt not_active IP Right Cessation
- 1986-04-19 KR KR1019860700918A patent/KR940005838B1/ko not_active IP Right Cessation
- 1986-04-19 AT AT86903293T patent/ATE92091T1/de active
- 1986-04-19 WO PCT/EP1986/000234 patent/WO1986006401A1/de active IP Right Grant
- 1986-04-19 JP JP61502823A patent/JPS62502624A/ja not_active Expired - Lifetime
- 1986-04-19 AU AU58602/86A patent/AU586687B2/en not_active Ceased
- 1986-04-19 DE DE8686903293T patent/DE3688774D1/de not_active Expired - Fee Related
- 1986-04-25 DD DD86289633A patent/DD257444A5/de not_active IP Right Cessation
- 1986-04-25 CA CA000507597A patent/CA1272017A/en not_active Expired - Fee Related
- 1986-12-22 FI FI865270A patent/FI865270A/fi not_active Application Discontinuation
- 1986-12-23 DK DK629686A patent/DK629686D0/da not_active Application Discontinuation
- 1986-12-23 NO NO865304A patent/NO865304L/no unknown
-
1989
- 1989-10-20 US US07/426,466 patent/US5064566A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| NO865304D0 (no) | 1986-12-23 |
| KR880700044A (ko) | 1988-02-15 |
| DE3515374A1 (de) | 1986-11-06 |
| KR940005838B1 (ko) | 1994-06-24 |
| WO1986006401A1 (en) | 1986-11-06 |
| AU5860286A (en) | 1986-11-18 |
| DD257444A5 (de) | 1988-06-15 |
| EP0220296B1 (de) | 1993-07-28 |
| DK629686A (da) | 1986-12-23 |
| JPS62502624A (ja) | 1987-10-08 |
| CA1272017A (en) | 1990-07-31 |
| DK629686D0 (da) | 1986-12-23 |
| BR8606648A (pt) | 1987-08-04 |
| FI865270A0 (fi) | 1986-12-22 |
| DE3688774D1 (de) | 1993-09-02 |
| US5064566A (en) | 1991-11-12 |
| FI865270A (fi) | 1986-12-22 |
| AU586687B2 (en) | 1989-07-20 |
| DE3515374C2 (de) | 1998-02-26 |
| EP0220296A1 (de) | 1987-05-06 |
| ATE92091T1 (de) | 1993-08-15 |
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