SU469264A3 - Способ получени нормальных слоев нематических жидких кристаллов - Google Patents
Способ получени нормальных слоев нематических жидких кристалловInfo
- Publication number
- SU469264A3 SU469264A3 SU1888507A SU1888507A SU469264A3 SU 469264 A3 SU469264 A3 SU 469264A3 SU 1888507 A SU1888507 A SU 1888507A SU 1888507 A SU1888507 A SU 1888507A SU 469264 A3 SU469264 A3 SU 469264A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- para
- acid
- layers
- nematic
- benzoic acid
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 10
- 239000004988 Nematic liquid crystal Substances 0.000 title 1
- -1 alkoxy radicals Chemical class 0.000 description 29
- 239000002253 acid Substances 0.000 description 25
- 239000000203 mixture Substances 0.000 description 19
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 15
- 239000005711 Benzoic acid Substances 0.000 description 13
- 150000003839 salts Chemical class 0.000 description 13
- 239000000374 eutectic mixture Substances 0.000 description 11
- 238000002844 melting Methods 0.000 description 11
- 150000003254 radicals Chemical class 0.000 description 11
- 239000011521 glass Substances 0.000 description 10
- 230000008018 melting Effects 0.000 description 10
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 10
- 235000010233 benzoic acid Nutrition 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 150000001735 carboxylic acids Chemical class 0.000 description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- CPEPWESLFZVUEP-UHFFFAOYSA-N 4-hexylbenzoic acid Chemical compound CCCCCCC1=CC=C(C(O)=O)C=C1 CPEPWESLFZVUEP-UHFFFAOYSA-N 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 125000004423 acyloxy group Chemical group 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- JRXXLCKWQFKACW-UHFFFAOYSA-N biphenylacetylene Chemical class C1=CC=CC=C1C#CC1=CC=CC=C1 JRXXLCKWQFKACW-UHFFFAOYSA-N 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
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 235000013985 cinnamic acid Nutrition 0.000 description 2
- WBYWAXJHAXSJNI-UHFFFAOYSA-N cinnamic acid group Chemical class C(C=CC1=CC=CC=C1)(=O)O WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 2
- 150000001564 phenyl benzoates Chemical class 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 150000001629 stilbenes Chemical class 0.000 description 2
- 235000021286 stilbenes Nutrition 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- SMNNDVUKAKPGDD-UHFFFAOYSA-N 2-butylbenzoic acid Chemical compound CCCCC1=CC=CC=C1C(O)=O SMNNDVUKAKPGDD-UHFFFAOYSA-N 0.000 description 1
- NVXIJHWKTUUWCT-UHFFFAOYSA-N 4-hexanoyloxybenzoic acid Chemical compound CCCCCC(=O)OC1=CC=C(C(O)=O)C=C1 NVXIJHWKTUUWCT-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000208202 Linaceae Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 241000406668 Loxodonta cyclotis Species 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000002262 Schiff base Substances 0.000 description 1
- 150000004753 Schiff bases Chemical class 0.000 description 1
- XVZHLBGBENZDQG-UHFFFAOYSA-N [4-[(4-methoxyphenyl)methylamino]phenyl] butanoate Chemical compound COC1=CC=C(CNC2=CC=C(C=C2)OC(CCC)=O)C=C1 XVZHLBGBENZDQG-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 230000001746 atrial effect Effects 0.000 description 1
- 125000005337 azoxy group Chemical group [N+]([O-])(=N*)* 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 150000001559 benzoic acids Chemical class 0.000 description 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000001734 carboxylic acid salts Chemical class 0.000 description 1
- RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 150000001841 cholesterols Chemical class 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 229910052705 radium Inorganic materials 0.000 description 1
- HCWPIIXVSYCSAN-UHFFFAOYSA-N radium atom Chemical compound [Ra] HCWPIIXVSYCSAN-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- YFZDLRVCXDBOPH-UHFFFAOYSA-N tetraheptylazanium Chemical compound CCCCCCC[N+](CCCCCCC)(CCCCCCC)CCCCCCC YFZDLRVCXDBOPH-UHFFFAOYSA-N 0.000 description 1
- GJSGYPDDPQRWPK-UHFFFAOYSA-N tetrapentylammonium Chemical compound CCCCC[N+](CCCCC)(CCCCC)CCCCC GJSGYPDDPQRWPK-UHFFFAOYSA-N 0.000 description 1
- CZMILNXHOAKSBR-UHFFFAOYSA-N tetraphenylazanium Chemical compound C1=CC=CC=C1[N+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CZMILNXHOAKSBR-UHFFFAOYSA-N 0.000 description 1
- USFPINLPPFWTJW-UHFFFAOYSA-N tetraphenylphosphonium Chemical compound C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 USFPINLPPFWTJW-UHFFFAOYSA-N 0.000 description 1
- OSBSFAARYOCBHB-UHFFFAOYSA-N tetrapropylammonium Chemical compound CCC[N+](CCC)(CCC)CCC OSBSFAARYOCBHB-UHFFFAOYSA-N 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N trans-stilbene Chemical class C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- SNDRYHUSDCHSDJ-UHFFFAOYSA-N tributyl(dodecyl)phosphanium Chemical compound CCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC SNDRYHUSDCHSDJ-UHFFFAOYSA-N 0.000 description 1
- SEACXNRNJAXIBM-UHFFFAOYSA-N triethyl(methyl)azanium Chemical compound CC[N+](C)(CC)CC SEACXNRNJAXIBM-UHFFFAOYSA-N 0.000 description 1
- PXIMQGSMXJFQOF-UHFFFAOYSA-N triphenyl(propan-2-yl)phosphanium Chemical compound C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C(C)C)C1=CC=CC=C1 PXIMQGSMXJFQOF-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
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K19/54—Additives having no specific mesophase characterised by their chemical composition
- C09K19/56—Aligning agents
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Liquid Crystal Substances (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2209127A DE2209127A1 (de) | 1972-02-26 | 1972-02-26 | Modifizierte nematische phasen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU469264A3 true SU469264A3 (ru) | 1975-04-30 |
Family
ID=5837180
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1888507A SU469264A3 (ru) | 1972-02-26 | 1973-02-23 | Способ получени нормальных слоев нематических жидких кристаллов |
Country Status (12)
| Country | Link |
|---|---|
| JP (1) | JPS4899085A (cg-RX-API-DMAC10.html) |
| AT (1) | AT326191B (cg-RX-API-DMAC10.html) |
| BE (1) | BE795849A (cg-RX-API-DMAC10.html) |
| CH (1) | CH585256A5 (cg-RX-API-DMAC10.html) |
| DD (1) | DD106762A5 (cg-RX-API-DMAC10.html) |
| DE (1) | DE2209127A1 (cg-RX-API-DMAC10.html) |
| FR (1) | FR2173301B1 (cg-RX-API-DMAC10.html) |
| GB (1) | GB1376115A (cg-RX-API-DMAC10.html) |
| IL (1) | IL41423A (cg-RX-API-DMAC10.html) |
| IT (1) | IT979477B (cg-RX-API-DMAC10.html) |
| NL (1) | NL7301300A (cg-RX-API-DMAC10.html) |
| SU (1) | SU469264A3 (cg-RX-API-DMAC10.html) |
Families Citing this family (181)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS498262A (cg-RX-API-DMAC10.html) * | 1972-05-11 | 1974-01-24 | ||
| JPS4986279A (cg-RX-API-DMAC10.html) * | 1972-12-23 | 1974-08-19 | ||
| JPS6024152B2 (ja) * | 1976-12-28 | 1985-06-11 | シャープ株式会社 | 液晶組成物 |
| DE2832112C2 (de) * | 1978-07-21 | 1985-06-05 | Merck Patent Gmbh, 6100 Darmstadt | Flüssigkristallines Dielektrikum |
| DE2918775A1 (de) | 1979-05-10 | 1980-11-20 | Merck Patent Gmbh | Diketone, verfahren zu ihrer herstellung und ihre verwendung als komponenten fluessigkristalliner dielektrika |
| US4528114A (en) * | 1981-12-18 | 1985-07-09 | Hoffmann-La Roche Inc. | Acetylenes |
| US4577931A (en) * | 1982-05-26 | 1986-03-25 | Epson Corporation | Liquid crystal composition |
| DE3407013A1 (de) | 1984-02-27 | 1985-09-05 | Merck Patent Gmbh, 6100 Darmstadt | Cyclohexanderivate |
| DE3600052A1 (de) | 1986-01-03 | 1987-07-09 | Merck Patent Gmbh | Heterocyclische verbindungen |
| DE3601452A1 (de) | 1986-01-20 | 1987-07-23 | Merck Patent Gmbh | Vinylen-verbindungen |
| DE10229828B4 (de) | 2001-07-31 | 2011-12-01 | Merck Patent Gmbh | Flüssigkristallines Medium und seine Verwendung |
| DE10216197B4 (de) | 2002-04-12 | 2013-02-07 | Merck Patent Gmbh | Flüssigkristallmedium und und seine Verwendung in einer elektrooptischen Anzeige |
| US7217445B2 (en) * | 2003-12-15 | 2007-05-15 | Nitto Denko Corporation | Aligned liquid crystal layer containing Lewis acids and process for increasing the tilt |
| US7989035B2 (en) | 2004-07-02 | 2011-08-02 | Merck Patent Gmbh | Liquid crystalline medium |
| US20070003709A1 (en) * | 2005-06-29 | 2007-01-04 | Nano Loa, Inc. | Liquid crystal display device |
| EP1764405A1 (en) * | 2005-09-20 | 2007-03-21 | Rolic AG | Functionalized photoreactive compounds |
| DE502007004908D1 (de) | 2006-10-12 | 2010-10-14 | Merck Patent Gmbh | Flüssigkristallanzeige |
| EP1958999B1 (de) | 2007-02-13 | 2012-07-11 | Merck Patent GmbH | Flüssigkristallines Medium |
| EP1959000B1 (de) | 2007-02-19 | 2010-07-07 | MERCK PATENT GmbH | Flüssigkristallines Medium |
| WO2009015744A1 (de) | 2007-07-30 | 2009-02-05 | Merck Patent Gmbh | Flüssigkristallanzeige |
| EP2176376B1 (de) | 2007-08-15 | 2012-09-19 | Merck Patent GmbH | Flüssigkristallines medium |
| KR101504379B1 (ko) | 2007-08-29 | 2015-03-19 | 메르크 파텐트 게엠베하 | 액정 디스플레이 |
| ATE530620T1 (de) | 2007-08-30 | 2011-11-15 | Merck Patent Gmbh | Flüssigkristallines medium |
| CN103820126B (zh) | 2007-08-30 | 2015-09-09 | 默克专利股份有限公司 | 液晶显示器 |
| US8313669B2 (en) | 2007-08-30 | 2012-11-20 | MERCK Patent Gesellschaft mit beschränkter Haftung | Liquid-crystal display |
| DE502008002792D1 (de) | 2007-09-07 | 2011-04-21 | Merck Patent Gmbh | Verfahren zur Herstellung einer homogenen flüssigen Mischung |
| US8114310B2 (en) | 2007-10-22 | 2012-02-14 | Merck Patent Gmbh | Liquid-crystal display |
| EP2065361B1 (de) | 2007-11-30 | 2014-12-17 | Merck Patent GmbH | Polymerisierbare Verbindungen |
| CN101978025B (zh) | 2008-03-25 | 2014-09-10 | 默克专利股份有限公司 | 液晶显示器 |
| EP2340292B1 (de) | 2008-10-29 | 2013-05-29 | Merck Patent GmbH | Flüssigkristallanzeige |
| EP2182046B1 (en) | 2008-10-30 | 2012-03-07 | Merck Patent GmbH | Liquid-crystalline medium and liquid crystal display |
| DE102008064171A1 (de) | 2008-12-22 | 2010-07-01 | Merck Patent Gmbh | Flüssigkristallines Medium |
| KR101648601B1 (ko) | 2008-12-22 | 2016-08-16 | 메르크 파텐트 게엠베하 | 액정 디스플레이 |
| DE102010006691A1 (de) | 2009-02-06 | 2010-10-28 | Merck Patent Gmbh | Flüssigkristallines Medium und Flüssigkristallanzeige |
| DE102010012900A1 (de) | 2009-04-23 | 2010-11-25 | Merck Patent Gmbh | Flüssigkristallanzeige |
| DE102009022309A1 (de) | 2009-05-22 | 2010-11-25 | Merck Patent Gmbh | Flüssigkristallanzeige |
| EP2292720A1 (en) | 2009-09-08 | 2011-03-09 | Merck Patent GmbH | Liquid-crystal display |
| DE102010035730A1 (de) | 2009-09-28 | 2011-04-07 | Merck Patent Gmbh | Polymerisierbare Verbindungen und ihre Verwendung in Flüssigkristallanzeigen |
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-
0
- BE BE795849D patent/BE795849A/xx unknown
-
1972
- 1972-02-26 DE DE2209127A patent/DE2209127A1/de active Pending
-
1973
- 1973-01-26 GB GB399573A patent/GB1376115A/en not_active Expired
- 1973-01-30 NL NL7301300A patent/NL7301300A/xx unknown
- 1973-01-30 IL IL41423A patent/IL41423A/en unknown
- 1973-02-21 CH CH245573A patent/CH585256A5/xx not_active IP Right Cessation
- 1973-02-23 SU SU1888507A patent/SU469264A3/ru active
- 1973-02-23 AT AT164173A patent/AT326191B/de not_active IP Right Cessation
- 1973-02-26 JP JP48022292A patent/JPS4899085A/ja active Pending
- 1973-02-26 IT IT20854/73A patent/IT979477B/it active
- 1973-02-26 DD DD169051A patent/DD106762A5/xx unknown
- 1973-02-26 FR FR7306674A patent/FR2173301B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE2209127A1 (de) | 1973-09-06 |
| IL41423A (en) | 1976-01-30 |
| AT326191B (de) | 1975-11-25 |
| FR2173301A1 (cg-RX-API-DMAC10.html) | 1973-10-05 |
| JPS4899085A (cg-RX-API-DMAC10.html) | 1973-12-15 |
| BE795849A (fr) | 1973-08-23 |
| DD106762A5 (cg-RX-API-DMAC10.html) | 1974-06-20 |
| FR2173301B1 (cg-RX-API-DMAC10.html) | 1976-06-11 |
| NL7301300A (cg-RX-API-DMAC10.html) | 1973-08-28 |
| IL41423A0 (en) | 1973-03-30 |
| GB1376115A (en) | 1974-12-04 |
| ATA164173A (de) | 1975-02-15 |
| CH585256A5 (cg-RX-API-DMAC10.html) | 1977-02-28 |
| IT979477B (it) | 1974-09-30 |
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