TW296392B - - Google Patents
Download PDFInfo
- Publication number
- TW296392B TW296392B TW83102939A TW83102939A TW296392B TW 296392 B TW296392 B TW 296392B TW 83102939 A TW83102939 A TW 83102939A TW 83102939 A TW83102939 A TW 83102939A TW 296392 B TW296392 B TW 296392B
- Authority
- TW
- Taiwan
- Prior art keywords
- group
- optically active
- patent application
- groups
- chemical formula
- Prior art date
Links
- 239000000126 substance Substances 0.000 claims description 39
- 229920000642 polymer Polymers 0.000 claims description 29
- 229920000515 polycarbonate Polymers 0.000 claims description 27
- 239000004417 polycarbonate Substances 0.000 claims description 27
- 150000001875 compounds Chemical class 0.000 claims description 17
- 108090000790 Enzymes Proteins 0.000 claims description 15
- 102000004190 Enzymes Human genes 0.000 claims description 15
- 238000011049 filling Methods 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 239000000178 monomer Substances 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 238000009833 condensation Methods 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 6
- -1 dihydroxytetrahydropyrrolyl Chemical group 0.000 claims description 4
- 229910052711 selenium Inorganic materials 0.000 claims description 4
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 230000005494 condensation Effects 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000001072 heteroaryl group Chemical group 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 238000006068 polycondensation reaction Methods 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 229940125717 barbiturate Drugs 0.000 claims 2
- HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 claims 2
- QGHDLJAZIIFENW-UHFFFAOYSA-N 4-[1,1,1,3,3,3-hexafluoro-2-(4-hydroxy-3-prop-2-enylphenyl)propan-2-yl]-2-prop-2-enylphenol Chemical group C1=C(CC=C)C(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C(CC=C)=C1 QGHDLJAZIIFENW-UHFFFAOYSA-N 0.000 claims 1
- MMWCQWOKHLEYSP-UHFFFAOYSA-N BisPhenol A bis(chloroformate) Chemical compound C=1C=C(OC(Cl)=O)C=CC=1C(C)(C)C1=CC=C(OC(Cl)=O)C=C1 MMWCQWOKHLEYSP-UHFFFAOYSA-N 0.000 claims 1
- 229920000547 conjugated polymer Polymers 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 1
- 239000013589 supplement Substances 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 30
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 15
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 14
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Substances C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 13
- 238000003756 stirring Methods 0.000 description 12
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 10
- 230000003287 optical effect Effects 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 7
- 239000002253 acid Substances 0.000 description 5
- 239000007795 chemical reaction product Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- 238000000855 fermentation Methods 0.000 description 3
- 230000004151 fermentation Effects 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000004528 spin coating Methods 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000000862 absorption spectrum Methods 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- FDJUMMKAFUMWBI-UHFFFAOYSA-N chloro carbonochloridate Chemical compound ClOC(Cl)=O FDJUMMKAFUMWBI-UHFFFAOYSA-N 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- KVGZZAHHUNAVKZ-UHFFFAOYSA-N 1,4-Dioxin Chemical group O1C=COC=C1 KVGZZAHHUNAVKZ-UHFFFAOYSA-N 0.000 description 1
- PRWKRSVNKQLMBN-UHFFFAOYSA-N 2-[2-(4-nitrophenyl)ethenyl]aniline Chemical compound NC1=C(C=CC=C1)C=CC1=CC=C(C=C1)[N+](=O)[O-] PRWKRSVNKQLMBN-UHFFFAOYSA-N 0.000 description 1
- BUGPQBVYSHUWQJ-UHFFFAOYSA-N 2-[n-(2-hydroxyethyl)-4-[2-(4-nitrophenyl)ethenyl]anilino]ethanol Chemical compound C1=CC(N(CCO)CCO)=CC=C1C=CC1=CC=C([N+]([O-])=O)C=C1 BUGPQBVYSHUWQJ-UHFFFAOYSA-N 0.000 description 1
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 1
- 125000006291 3-hydroxybenzyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(=C1[H])C([H])([H])* 0.000 description 1
- ZYUVGYBAPZYKSA-UHFFFAOYSA-N 5-(3-hydroxybutan-2-yl)-4-methylbenzene-1,3-diol Chemical compound CC(O)C(C)C1=CC(O)=CC(O)=C1C ZYUVGYBAPZYKSA-UHFFFAOYSA-N 0.000 description 1
- GSNUFIFRDBKVIE-UHFFFAOYSA-N DMF Natural products CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 208000001613 Gambling Diseases 0.000 description 1
- 235000005206 Hibiscus Nutrition 0.000 description 1
- 235000007185 Hibiscus lunariifolius Nutrition 0.000 description 1
- 244000284380 Hibiscus rosa sinensis Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000003283 Pachira macrocarpa Nutrition 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 230000005697 Pockels effect Effects 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical group [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 206010041349 Somnolence Diseases 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- 240000001085 Trapa natans Species 0.000 description 1
- 235000014364 Trapa natans Nutrition 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- ZFVMWEVVKGLCIJ-UHFFFAOYSA-N bisphenol AF Chemical compound C1=CC(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C=C1 ZFVMWEVVKGLCIJ-UHFFFAOYSA-N 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 125000002993 cycloalkylene group Chemical group 0.000 description 1
- 230000001086 cytosolic effect Effects 0.000 description 1
- NHADDZMCASKINP-HTRCEHHLSA-N decarboxydihydrocitrinin Natural products C1=C(O)C(C)=C2[C@H](C)[C@@H](C)OCC2=C1O NHADDZMCASKINP-HTRCEHHLSA-N 0.000 description 1
- 125000003963 dichloro group Chemical group Cl* 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- CJMJLDQKTOJACI-BGQAIRJTSA-N ergotamine d-tartrate Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O.C([C@H]1C(=O)N2CCC[C@H]2[C@]2(O)O[C@@](C(N21)=O)(C)NC(=O)[C@H]1CN([C@H]2C(C=3C=CC=C4NC=C(C=34)C2)=C1)C)C1=CC=CC=C1.C([C@H]1C(=O)N2CCC[C@H]2[C@]2(O)O[C@@](C(N21)=O)(C)NC(=O)[C@H]1CN([C@H]2C(C=3C=CC=C4NC=C(C=34)C2)=C1)C)C1=CC=CC=C1 CJMJLDQKTOJACI-BGQAIRJTSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- WGKXMQMRNAHMHZ-UHFFFAOYSA-N formic acid phenol Chemical compound C(=O)O.C1(=CC=CC=C1)O.C1(=CC=CC=C1)O WGKXMQMRNAHMHZ-UHFFFAOYSA-N 0.000 description 1
- 125000003250 fulvenyl group Chemical group C1(=CC=CC1=C)* 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 150000007965 phenolic acids Chemical class 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 235000009165 saligot Nutrition 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 235000015170 shellfish Nutrition 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000003554 tetrahydropyrrolyl group Chemical group 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/35—Non-linear optics
- G02F1/355—Non-linear optics characterised by the materials used
- G02F1/361—Organic materials
- G02F1/3615—Organic materials containing polymers
- G02F1/3617—Organic materials containing polymers having the non-linear optical group in a side chain
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/675—Low-molecular-weight compounds
- C08G18/677—Low-molecular-weight compounds containing heteroatoms other than oxygen and the nitrogen of primary or secondary amino groups
- C08G18/678—Low-molecular-weight compounds containing heteroatoms other than oxygen and the nitrogen of primary or secondary amino groups containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/773—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur halogens
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/83—Chemically modified polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/682—Polyesters containing atoms other than carbon, hydrogen and oxygen containing halogens
- C08G63/6824—Polyesters containing atoms other than carbon, hydrogen and oxygen containing halogens derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/6826—Dicarboxylic acids and dihydroxy compounds
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31507—Of polycarbonate
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nonlinear Science (AREA)
- General Chemical & Material Sciences (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Polyesters Or Polycarbonates (AREA)
- Optical Modulation, Optical Deflection, Nonlinear Optics, Optical Demodulation, Optical Logic Elements (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL9301679 | 1993-09-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW296392B true TW296392B (en, 2012) | 1997-01-21 |
Family
ID=19862941
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW83102939A TW296392B (en, 2012) | 1993-09-29 | 1994-04-02 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US5588083A (en, 2012) |
| EP (1) | EP0645413A1 (en, 2012) |
| JP (1) | JPH07165898A (en, 2012) |
| KR (1) | KR950008559A (en, 2012) |
| CA (1) | CA2133142A1 (en, 2012) |
| TW (1) | TW296392B (en, 2012) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69614051T2 (de) * | 1995-03-13 | 2002-04-18 | Jds Uniphase Photonics C.V., Arnheim/Arnhem | Vernetzte oder vernetzbare optische polycarbonate und optische komponenten enthaltend diese optische polycarbonate |
| KR19990014683A (ko) * | 1995-06-28 | 1999-02-25 | 샬크비즈크 피이터 코르넬리스, 페트 귄터 | 5층식 광학장치 |
| US5776374A (en) * | 1995-11-07 | 1998-07-07 | The Dow Chemical Company | Crosslinkable thermoplastic and crosslinked thermoset nonlinear optical polymeric compositions derived from aromatic dihydroxy compounds |
| EP0780722A1 (en) * | 1995-12-22 | 1997-06-25 | Akzo Nobel N.V. | Electro-optical device stable in the 600-1600 nanometer wavelength range |
| US5732693A (en) | 1996-10-02 | 1998-03-31 | Ohmeda Inc. | Pause control of nitric oxide therapy |
| AU4867297A (en) * | 1996-10-23 | 1998-05-15 | Akzo Nobel N.V. | Cross-linkers for cross-linkable optical polycarbonates |
| US6470131B1 (en) | 2000-11-03 | 2002-10-22 | Corning Incorporated | Highly-halogenated low optical loss polymer |
| US6782154B2 (en) | 2001-02-12 | 2004-08-24 | Rensselaer Polytechnic Institute | Ultrafast all-optical switch using carbon nanotube polymer composites |
| US6614977B2 (en) * | 2001-07-12 | 2003-09-02 | Little Optics, Inc. | Use of deuterated gases for the vapor deposition of thin films for low-loss optical devices and waveguides |
| US7043133B2 (en) * | 2001-07-12 | 2006-05-09 | Little Optics, Inc. | Silicon-oxycarbide high index contrast, low-loss optical waveguides and integrated thermo-optic devices |
| WO2003034102A2 (en) * | 2001-10-16 | 2003-04-24 | Lightwave Microsystems Corporation | Waveplate and optical circuit formed from mesogen-containing polymer |
| US6654188B2 (en) * | 2001-12-12 | 2003-11-25 | Lightspan, Llc | Compositions and devices for thermo optically controlled switching and filtering |
| US8173045B2 (en) | 2008-05-28 | 2012-05-08 | University Of Washington | Diels-Alder crosslinkable dendritic nonlinear optic chromophores and polymer composites |
| WO2015193865A1 (en) | 2014-06-20 | 2015-12-23 | Sabic Global Technologies B.V. | Processes for designing cross-linkable polycarbonates and articles formed therefrom |
| CN111040186B (zh) * | 2019-12-27 | 2020-11-17 | 华中科技大学 | 一种ab2型二阶非线性光学超支化聚合物、其制备和应用 |
| JP7357881B2 (ja) * | 2020-07-02 | 2023-10-10 | 帝人株式会社 | 電気光学効果を有するポリカーボネート及びその製造方法、並びに該ポリカーボネートを用いた光制御素子 |
| EP4389779A1 (en) * | 2021-08-20 | 2024-06-26 | National Institute of Information and Communications Technology | Polymer and light control device |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4666819A (en) * | 1985-03-11 | 1987-05-19 | Minnesota Mining And Manufacturing Company | Optical information storage based on polymeric dyes |
| US4859876A (en) * | 1985-09-16 | 1989-08-22 | AT&T Bell Laboratories American Telephone and Telegraph Company | Nonlinear optical materials and devices |
| US4757130A (en) * | 1987-07-01 | 1988-07-12 | Hoechst Celanese Corporaton | Condensation polymers with pendant side chains exhibiting nonlinear optical response |
| US5001209A (en) * | 1988-07-04 | 1991-03-19 | Akzo N.V. | Non-linear optical active diols and polyurethanes prepared therefrom |
| EP0358476B1 (en) * | 1988-09-08 | 1998-07-22 | Akzo Nobel N.V. | Integrated optic components |
| US5093456A (en) * | 1989-06-14 | 1992-03-03 | Minnesota Mining And Manufacturing Company | Monocarbamate diols, polymers derived from them and nlo-active materials therefrom |
| FR2657083A1 (fr) * | 1990-01-15 | 1991-07-19 | Rhone Poulenc Chimie | Polyesters actifs en optique non lineaire et materiaux les contenant dispositif optique les contenant et procedes de fabrication de ces composes et materiaux. |
| DE69108117T2 (de) * | 1990-07-06 | 1995-11-16 | Nippon Telegraph & Telephone | Nichtlineare optische Materialien und Vorrichtungen. |
| US5395556A (en) * | 1990-12-12 | 1995-03-07 | Enichem S.P.A. | Tricyanovinyl substitution process for NLO polymers |
| US5208299A (en) * | 1992-04-10 | 1993-05-04 | The Dow Chemical Company | Nonlinear optical arylhydrazones and nonlinear optical polymers thereof |
| US5359008A (en) * | 1992-05-18 | 1994-10-25 | Nippon Telegraph And Telephone Corporation | Second-order nonlinear optical polymer and method for producing the same |
| JPH08501811A (ja) * | 1992-07-06 | 1996-02-27 | アクゾ ノーベル ナムローゼ フェンノートシャップ | 高いガラス転移温度を有する非線形光学活性ポリウレタン |
-
1994
- 1994-04-02 TW TW83102939A patent/TW296392B/zh active
- 1994-09-22 EP EP19940202733 patent/EP0645413A1/en not_active Withdrawn
- 1994-09-26 US US08/312,254 patent/US5588083A/en not_active Expired - Fee Related
- 1994-09-28 CA CA 2133142 patent/CA2133142A1/en not_active Abandoned
- 1994-09-28 KR KR1019940025245A patent/KR950008559A/ko not_active Withdrawn
- 1994-09-29 JP JP25924994A patent/JPH07165898A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| KR950008559A (ko) | 1995-04-19 |
| EP0645413A1 (en) | 1995-03-29 |
| US5588083A (en) | 1996-12-24 |
| CA2133142A1 (en) | 1995-03-30 |
| JPH07165898A (ja) | 1995-06-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TW296392B (en, 2012) | ||
| US7067566B2 (en) | Triazine ring based polymers for photoinduced liquid crystal alignment, liquid crystal alignment layer containing the same, liquid crystal element using the alignment layer and method of manufacturing the same | |
| TWI259192B (en) | Diaminobenzene derivative, polyimide obtained therefrom, and liquid-crystal alignment film | |
| JP3210341B2 (ja) | 非線形光学性ポリマー組成物、その製造方法並びにそれから得られる非線形光学材料および物品 | |
| TWI642726B (zh) | 液晶配向劑、液晶配向膜以及液晶顯示元件 | |
| Nemoto et al. | Novel types of polyesters containing second-order nonlinear optically active chromophores with high density | |
| TW201430060A (zh) | 液晶配向劑、液晶配向膜、液晶顯示元件及反應產物 | |
| TWI591125B (zh) | 液晶配向劑、液晶配向膜、液晶顯示元件、聚合物以及化合物 | |
| US5670603A (en) | Polymers exhibiting nonlinear optical properties | |
| CN101539688A (zh) | 液晶取向剂和液晶显示元件 | |
| TW311990B (en, 2012) | ||
| JP7582305B2 (ja) | 液晶配向剤、液晶配向膜、及び液晶表示素子 | |
| JP2882630B2 (ja) | 光配向性高分子及びこれより形成された配向膜並びに該配向膜を具備した液晶表示素子 | |
| KR101598545B1 (ko) | 폴리아미드계 광반응성 중합체 및 이의 제조 방법 | |
| JPH03121114A (ja) | 非線形光学活性有機物質およびこの物質からなる要素を含む装置 | |
| CN113939764B (zh) | 液晶取向剂、液晶取向膜、液晶元件、聚合物及化合物 | |
| US20060157672A1 (en) | Process For Producing Optically Active Liquid Crystalline Polymer Compound | |
| US7670512B2 (en) | Second order nonlinear optical polyimides having benzobisthiazole-based pendant groups, and preparation of the same | |
| KR100216004B1 (ko) | 이차 비선형 광학 특성을 갖는 이타코네이트 공중합체 | |
| JPH04297470A (ja) | 非線形光学特性を有する網状化エポキシ樹脂 | |
| Ballet et al. | Chromophore‐Functionalized Poly (ether sulfone) s with High Poling Stabilities of the Nonlinear Optical Effect | |
| JP7694561B2 (ja) | 新規ジアミン、重合体、液晶配向剤、液晶配向膜、及びそれを用いた液晶表示素子 | |
| Nemoto et al. | Polyamides for nonlinear optics containing second-order NLO-phores with high density | |
| KR101387737B1 (ko) | 액정 배향제, 이를 이용하여 제조한 액정 배향막, 및 상기 액정 배향막을 포함하는 액정표시소자 | |
| JP7533470B2 (ja) | 液晶配向剤、液晶配向膜、及び液晶表示素子 |