JP2014196265A - 重合性化合物及び光学素子 - Google Patents
重合性化合物及び光学素子 Download PDFInfo
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- JP2014196265A JP2014196265A JP2013072526A JP2013072526A JP2014196265A JP 2014196265 A JP2014196265 A JP 2014196265A JP 2013072526 A JP2013072526 A JP 2013072526A JP 2013072526 A JP2013072526 A JP 2013072526A JP 2014196265 A JP2014196265 A JP 2014196265A
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- CCVKPWUMYBYHCD-UHFFFAOYSA-N oxolane;pyridine Chemical compound C1CCOC1.C1=CC=NC=C1 CCVKPWUMYBYHCD-UHFFFAOYSA-N 0.000 description 1
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- 125000006505 p-cyanobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C#N)C([H])([H])* 0.000 description 1
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- 125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
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- VUYVXCJTTQJVKJ-UHFFFAOYSA-L palladium(2+);tricyclohexylphosphane;dichloride Chemical compound Cl[Pd]Cl.C1CCCCC1P(C1CCCCC1)C1CCCCC1.C1CCCCC1P(C1CCCCC1)C1CCCCC1 VUYVXCJTTQJVKJ-UHFFFAOYSA-L 0.000 description 1
- OTYPIDNRISCWQY-UHFFFAOYSA-L palladium(2+);tris(2-methylphenyl)phosphane;dichloride Chemical compound Cl[Pd]Cl.CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C.CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C OTYPIDNRISCWQY-UHFFFAOYSA-L 0.000 description 1
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- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 1
- JKDRQYIYVJVOPF-FDGPNNRMSA-L palladium(ii) acetylacetonate Chemical compound [Pd+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O JKDRQYIYVJVOPF-FDGPNNRMSA-L 0.000 description 1
- QJPQVXSHYBGQGM-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 QJPQVXSHYBGQGM-UHFFFAOYSA-N 0.000 description 1
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- IGEIPFLJVCPEKU-UHFFFAOYSA-N pentan-2-amine Chemical compound CCCC(C)N IGEIPFLJVCPEKU-UHFFFAOYSA-N 0.000 description 1
- SNGREZUHAYWORS-UHFFFAOYSA-N perfluorooctanoic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SNGREZUHAYWORS-UHFFFAOYSA-N 0.000 description 1
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- CXVZSCNFUYXXIS-UHFFFAOYSA-N phosphono 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OP(O)(O)=O CXVZSCNFUYXXIS-UHFFFAOYSA-N 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 208000017983 photosensitivity disease Diseases 0.000 description 1
- 231100000434 photosensitization Toxicity 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
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- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- WFIZEGIEIOHZCP-UHFFFAOYSA-M potassium formate Chemical compound [K+].[O-]C=O WFIZEGIEIOHZCP-UHFFFAOYSA-M 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- CUQOHAYJWVTKDE-UHFFFAOYSA-N potassium;butan-1-olate Chemical compound [K+].CCCC[O-] CUQOHAYJWVTKDE-UHFFFAOYSA-N 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- KCXFHTAICRTXLI-UHFFFAOYSA-N propane-1-sulfonic acid Chemical compound CCCS(O)(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-N 0.000 description 1
- 125000001325 propanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- HFJXYNUVULQBTH-UHFFFAOYSA-N pyrimidine;quinoline Chemical compound C1=CN=CN=C1.N1=CC=CC2=CC=CC=C21 HFJXYNUVULQBTH-UHFFFAOYSA-N 0.000 description 1
- LHGVFZTZFXWLCP-UHFFFAOYSA-N pyrocatechol monomethyl ether Natural products COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 1
- 150000003232 pyrogallols Chemical class 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- SBYHFKPVCBCYGV-UHFFFAOYSA-N quinuclidine Chemical compound C1CC2CCN1CC2 SBYHFKPVCBCYGV-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
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- 150000007949 saponins Chemical class 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
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- NRHMKIHPTBHXPF-TUJRSCDTSA-M sodium cholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 NRHMKIHPTBHXPF-TUJRSCDTSA-M 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
- 229940045845 sodium myristate Drugs 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 229940045870 sodium palmitate Drugs 0.000 description 1
- 229940006186 sodium polystyrene sulfonate Drugs 0.000 description 1
- 229910000031 sodium sesquicarbonate Inorganic materials 0.000 description 1
- 235000018341 sodium sesquicarbonate Nutrition 0.000 description 1
- 229940080350 sodium stearate Drugs 0.000 description 1
- LLHSEQCZSNZLRI-UHFFFAOYSA-M sodium;3,5-bis(methoxycarbonyl)benzenesulfonate Chemical compound [Na+].COC(=O)C1=CC(C(=O)OC)=CC(S([O-])(=O)=O)=C1 LLHSEQCZSNZLRI-UHFFFAOYSA-M 0.000 description 1
- PNGLEYLFMHGIQO-UHFFFAOYSA-M sodium;3-(n-ethyl-3-methoxyanilino)-2-hydroxypropane-1-sulfonate;dihydrate Chemical compound O.O.[Na+].[O-]S(=O)(=O)CC(O)CN(CC)C1=CC=CC(OC)=C1 PNGLEYLFMHGIQO-UHFFFAOYSA-M 0.000 description 1
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
- PNGBYKXZVCIZRN-UHFFFAOYSA-M sodium;hexadecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCCCCCS([O-])(=O)=O PNGBYKXZVCIZRN-UHFFFAOYSA-M 0.000 description 1
- GGXKEBACDBNFAF-UHFFFAOYSA-M sodium;hexadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCC([O-])=O GGXKEBACDBNFAF-UHFFFAOYSA-M 0.000 description 1
- GGHPAKFFUZUEKL-UHFFFAOYSA-M sodium;hexadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCOS([O-])(=O)=O GGHPAKFFUZUEKL-UHFFFAOYSA-M 0.000 description 1
- KBAFDSIZQYCDPK-UHFFFAOYSA-M sodium;octadecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCCCCCCCS([O-])(=O)=O KBAFDSIZQYCDPK-UHFFFAOYSA-M 0.000 description 1
- PLQISZLZPSPBDP-UHFFFAOYSA-M sodium;pentadecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCCCCS([O-])(=O)=O PLQISZLZPSPBDP-UHFFFAOYSA-M 0.000 description 1
- AYFACLKQYVTXNS-UHFFFAOYSA-M sodium;tetradecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCCCS([O-])(=O)=O AYFACLKQYVTXNS-UHFFFAOYSA-M 0.000 description 1
- JUQGWKYSEXPRGL-UHFFFAOYSA-M sodium;tetradecanoate Chemical compound [Na+].CCCCCCCCCCCCCC([O-])=O JUQGWKYSEXPRGL-UHFFFAOYSA-M 0.000 description 1
- CACJZDMMUHMEBN-UHFFFAOYSA-M sodium;tridecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCCS([O-])(=O)=O CACJZDMMUHMEBN-UHFFFAOYSA-M 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 235000011067 sorbitan monolaureate Nutrition 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 235000011071 sorbitan monopalmitate Nutrition 0.000 description 1
- 239000001570 sorbitan monopalmitate Substances 0.000 description 1
- 229940031953 sorbitan monopalmitate Drugs 0.000 description 1
- 229960005078 sorbitan sesquioleate Drugs 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- UUCCCPNEFXQJEL-UHFFFAOYSA-L strontium dihydroxide Chemical compound [OH-].[OH-].[Sr+2] UUCCCPNEFXQJEL-UHFFFAOYSA-L 0.000 description 1
- 229910001866 strontium hydroxide Inorganic materials 0.000 description 1
- 229940120904 succinylcholine chloride Drugs 0.000 description 1
- YOEWQQVKRJEPAE-UHFFFAOYSA-L succinylcholine chloride (anhydrous) Chemical compound [Cl-].[Cl-].C[N+](C)(C)CCOC(=O)CCC(=O)OCC[N+](C)(C)C YOEWQQVKRJEPAE-UHFFFAOYSA-L 0.000 description 1
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- HDVYDCKEPDMCAF-UHFFFAOYSA-N tetrabutylammonium bromodiiodide Chemical compound Br[I-]I.CCCC[N+](CCCC)(CCCC)CCCC HDVYDCKEPDMCAF-UHFFFAOYSA-N 0.000 description 1
- LSCNDUNMPYESRN-UHFFFAOYSA-N tetrabutylammonium dibromochloride Chemical compound Br[Cl-]Br.CCCC[N+](CCCC)(CCCC)CCCC LSCNDUNMPYESRN-UHFFFAOYSA-N 0.000 description 1
- LFZGDXLUTJIZAG-UHFFFAOYSA-N tetrabutylammonium dibromoiodide Chemical compound Br[I-]Br.CCCC[N+](CCCC)(CCCC)CCCC LFZGDXLUTJIZAG-UHFFFAOYSA-N 0.000 description 1
- XKVIJLXGNLMYCT-UHFFFAOYSA-N tetrabutylammonium dichlorobromide Chemical compound Cl[Br-]Cl.CCCC[N+](CCCC)(CCCC)CCCC XKVIJLXGNLMYCT-UHFFFAOYSA-N 0.000 description 1
- YUISSJZXEJELPR-UHFFFAOYSA-L tetrabutylazanium tetraethylazanium diiodide Chemical compound C(C)[N+](CC)(CC)CC.C(CCC)[N+](CCCC)(CCCC)CCCC.[I-].[I-] YUISSJZXEJELPR-UHFFFAOYSA-L 0.000 description 1
- MCZDHTKJGDCTAE-UHFFFAOYSA-M tetrabutylazanium;acetate Chemical compound CC([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC MCZDHTKJGDCTAE-UHFFFAOYSA-M 0.000 description 1
- GMRIOAVKKGNMMV-UHFFFAOYSA-N tetrabutylazanium;azide Chemical compound [N-]=[N+]=[N-].CCCC[N+](CCCC)(CCCC)CCCC GMRIOAVKKGNMMV-UHFFFAOYSA-N 0.000 description 1
- MRXQMNWIADOAJY-UHFFFAOYSA-M tetrabutylazanium;fluoride;dihydrofluoride Chemical compound F.F.[F-].CCCC[N+](CCCC)(CCCC)CCCC MRXQMNWIADOAJY-UHFFFAOYSA-M 0.000 description 1
- KBLZDCFTQSIIOH-UHFFFAOYSA-M tetrabutylazanium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC KBLZDCFTQSIIOH-UHFFFAOYSA-M 0.000 description 1
- RSHBFZCIFFBTEW-UHFFFAOYSA-M tetrabutylazanium;thiocyanate Chemical compound [S-]C#N.CCCC[N+](CCCC)(CCCC)CCCC RSHBFZCIFFBTEW-UHFFFAOYSA-M 0.000 description 1
- SFLXUZPXEWWQNH-UHFFFAOYSA-K tetrabutylazanium;tribromide Chemical compound [Br-].[Br-].[Br-].CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC SFLXUZPXEWWQNH-UHFFFAOYSA-K 0.000 description 1
- YNJQKNVVBBIPBA-UHFFFAOYSA-M tetrabutylazanium;trifluoromethanesulfonate Chemical compound [O-]S(=O)(=O)C(F)(F)F.CCCC[N+](CCCC)(CCCC)CCCC YNJQKNVVBBIPBA-UHFFFAOYSA-M 0.000 description 1
- SBSSZSCMFDYICE-UHFFFAOYSA-N tetrabutylazanium;triiodide Chemical compound I[I-]I.CCCC[N+](CCCC)(CCCC)CCCC SBSSZSCMFDYICE-UHFFFAOYSA-N 0.000 description 1
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- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 1
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- 229940073455 tetraethylammonium hydroxide Drugs 0.000 description 1
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- LRGJRHZIDJQFCL-UHFFFAOYSA-M tetraethylazanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)CC LRGJRHZIDJQFCL-UHFFFAOYSA-M 0.000 description 1
- WGHUNMFFLAMBJD-UHFFFAOYSA-M tetraethylazanium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.CC[N+](CC)(CC)CC WGHUNMFFLAMBJD-UHFFFAOYSA-M 0.000 description 1
- PUZYNDBTWXJXKN-UHFFFAOYSA-M tetraethylazanium;trifluoromethanesulfonate Chemical compound [O-]S(=O)(=O)C(F)(F)F.CC[N+](CC)(CC)CC PUZYNDBTWXJXKN-UHFFFAOYSA-M 0.000 description 1
- YQIVQBMEBZGFBY-UHFFFAOYSA-M tetraheptylazanium;bromide Chemical compound [Br-].CCCCCCC[N+](CCCCCCC)(CCCCCCC)CCCCCCC YQIVQBMEBZGFBY-UHFFFAOYSA-M 0.000 description 1
- KCSOHLKZTZMKQA-UHFFFAOYSA-M tetraheptylazanium;iodide Chemical compound [I-].CCCCCCC[N+](CCCCCCC)(CCCCCCC)CCCCCCC KCSOHLKZTZMKQA-UHFFFAOYSA-M 0.000 description 1
- VRKHAMWCGMJAMI-UHFFFAOYSA-M tetrahexylazanium;iodide Chemical compound [I-].CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC VRKHAMWCGMJAMI-UHFFFAOYSA-M 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
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- AHNISXOXSNAHBZ-UHFFFAOYSA-M tetrakis-decylazanium;bromide Chemical compound [Br-].CCCCCCCCCC[N+](CCCCCCCCCC)(CCCCCCCCCC)CCCCCCCCCC AHNISXOXSNAHBZ-UHFFFAOYSA-M 0.000 description 1
- DDFYFBUWEBINLX-UHFFFAOYSA-M tetramethylammonium bromide Chemical compound [Br-].C[N+](C)(C)C DDFYFBUWEBINLX-UHFFFAOYSA-M 0.000 description 1
- MRYQZMHVZZSQRT-UHFFFAOYSA-M tetramethylazanium;acetate Chemical compound CC([O-])=O.C[N+](C)(C)C MRYQZMHVZZSQRT-UHFFFAOYSA-M 0.000 description 1
- RXMRGBVLCSYIBO-UHFFFAOYSA-M tetramethylazanium;iodide Chemical compound [I-].C[N+](C)(C)C RXMRGBVLCSYIBO-UHFFFAOYSA-M 0.000 description 1
- ZCWKIFAQRXNZCH-UHFFFAOYSA-M tetramethylazanium;perchlorate Chemical compound C[N+](C)(C)C.[O-]Cl(=O)(=O)=O ZCWKIFAQRXNZCH-UHFFFAOYSA-M 0.000 description 1
- KJFVITRRNTVAPC-UHFFFAOYSA-L tetramethylazanium;sulfate Chemical compound C[N+](C)(C)C.C[N+](C)(C)C.[O-]S([O-])(=O)=O KJFVITRRNTVAPC-UHFFFAOYSA-L 0.000 description 1
- QBVXKDJEZKEASM-UHFFFAOYSA-M tetraoctylammonium bromide Chemical compound [Br-].CCCCCCCC[N+](CCCCCCCC)(CCCCCCCC)CCCCCCCC QBVXKDJEZKEASM-UHFFFAOYSA-M 0.000 description 1
- SPALIFXDWQTXKS-UHFFFAOYSA-M tetrapentylazanium;bromide Chemical compound [Br-].CCCCC[N+](CCCCC)(CCCCC)CCCCC SPALIFXDWQTXKS-UHFFFAOYSA-M 0.000 description 1
- SXAWRMKQZKPHNJ-UHFFFAOYSA-M tetrapentylazanium;chloride Chemical compound [Cl-].CCCCC[N+](CCCCC)(CCCCC)CCCCC SXAWRMKQZKPHNJ-UHFFFAOYSA-M 0.000 description 1
- FBLZDUAOBOMSNZ-UHFFFAOYSA-M tetrapentylazanium;iodide Chemical compound [I-].CCCCC[N+](CCCCC)(CCCCC)CCCCC FBLZDUAOBOMSNZ-UHFFFAOYSA-M 0.000 description 1
- OSBSFAARYOCBHB-UHFFFAOYSA-N tetrapropylammonium Chemical compound CCC[N+](CCC)(CCC)CCC OSBSFAARYOCBHB-UHFFFAOYSA-N 0.000 description 1
- BGQMOFGZRJUORO-UHFFFAOYSA-M tetrapropylammonium bromide Chemical compound [Br-].CCC[N+](CCC)(CCC)CCC BGQMOFGZRJUORO-UHFFFAOYSA-M 0.000 description 1
- FBEVECUEMUUFKM-UHFFFAOYSA-M tetrapropylazanium;chloride Chemical compound [Cl-].CCC[N+](CCC)(CCC)CCC FBEVECUEMUUFKM-UHFFFAOYSA-M 0.000 description 1
- LPSKDVINWQNWFE-UHFFFAOYSA-M tetrapropylazanium;hydroxide Chemical compound [OH-].CCC[N+](CCC)(CCC)CCC LPSKDVINWQNWFE-UHFFFAOYSA-M 0.000 description 1
- 229910021515 thallium hydroxide Inorganic materials 0.000 description 1
- QGYXCSSUHCHXHB-UHFFFAOYSA-M thallium(i) hydroxide Chemical compound [OH-].[Tl+] QGYXCSSUHCHXHB-UHFFFAOYSA-M 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- JTNXQVCPQMQLHK-UHFFFAOYSA-N thioacetone Chemical group CC(C)=S JTNXQVCPQMQLHK-UHFFFAOYSA-N 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- SFKTYEXKZXBQRQ-UHFFFAOYSA-J thorium(4+);tetrahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[Th+4] SFKTYEXKZXBQRQ-UHFFFAOYSA-J 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 125000005147 toluenesulfonyl group Chemical group C=1(C(=CC=CC1)S(=O)(=O)*)C 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- DWWMSEANWMWMCB-UHFFFAOYSA-N tribromomethylsulfonylbenzene Chemical compound BrC(Br)(Br)S(=O)(=O)C1=CC=CC=C1 DWWMSEANWMWMCB-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- FXNJNGMYIZRQRG-UHFFFAOYSA-N tridecan-7-amine Chemical compound CCCCCCC(N)CCCCCC FXNJNGMYIZRQRG-UHFFFAOYSA-N 0.000 description 1
- SWZDQOUHBYYPJD-UHFFFAOYSA-N tridodecylamine Chemical compound CCCCCCCCCCCCN(CCCCCCCCCCCC)CCCCCCCCCCCC SWZDQOUHBYYPJD-UHFFFAOYSA-N 0.000 description 1
- AJSTXXYNEIHPMD-UHFFFAOYSA-N triethyl borate Chemical compound CCOB(OCC)OCC AJSTXXYNEIHPMD-UHFFFAOYSA-N 0.000 description 1
- XQDHXDORJFXNDX-UHFFFAOYSA-M triethyl(2-hydroxyethyl)azanium;iodide Chemical compound [I-].CC[N+](CC)(CC)CCO XQDHXDORJFXNDX-UHFFFAOYSA-M 0.000 description 1
- NIUZJTWSUGSWJI-UHFFFAOYSA-M triethyl(methyl)azanium;chloride Chemical compound [Cl-].CC[N+](C)(CC)CC NIUZJTWSUGSWJI-UHFFFAOYSA-M 0.000 description 1
- WMSWXWGJYOIACA-UHFFFAOYSA-M triethyl(phenyl)azanium;iodide Chemical compound [I-].CC[N+](CC)(CC)C1=CC=CC=C1 WMSWXWGJYOIACA-UHFFFAOYSA-M 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- ZZJNLOGMYQURDL-UHFFFAOYSA-M trifluoromethanesulfonate;tris(4-methylphenyl)sulfanium Chemical compound [O-]S(=O)(=O)C(F)(F)F.C1=CC(C)=CC=C1[S+](C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 ZZJNLOGMYQURDL-UHFFFAOYSA-M 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
- WZGVRXXJKGXOBR-UHFFFAOYSA-N trihexadecyl borate Chemical compound CCCCCCCCCCCCCCCCOB(OCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCC WZGVRXXJKGXOBR-UHFFFAOYSA-N 0.000 description 1
- KDQYHGMMZKMQAA-UHFFFAOYSA-N trihexyl borate Chemical compound CCCCCCOB(OCCCCCC)OCCCCCC KDQYHGMMZKMQAA-UHFFFAOYSA-N 0.000 description 1
- MJOPOXYNSSGQHL-UHFFFAOYSA-M trimethyl(2-naphthalen-2-yloxycarbonyloxyethyl)azanium;iodide Chemical compound [I-].C1=CC=CC2=CC(OC(=O)OCC[N+](C)(C)C)=CC=C21 MJOPOXYNSSGQHL-UHFFFAOYSA-M 0.000 description 1
- JMCRETWEZLOFQT-UHFFFAOYSA-M trimethyl(3-triethoxysilylpropyl)azanium;chloride Chemical compound [Cl-].CCO[Si](OCC)(OCC)CCC[N+](C)(C)C JMCRETWEZLOFQT-UHFFFAOYSA-M 0.000 description 1
- SZEMGTQCPRNXEG-UHFFFAOYSA-M trimethyl(octadecyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C SZEMGTQCPRNXEG-UHFFFAOYSA-M 0.000 description 1
- AQZSPJRLCJSOED-UHFFFAOYSA-M trimethyl(octyl)azanium;chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(C)C AQZSPJRLCJSOED-UHFFFAOYSA-M 0.000 description 1
- GNMJFQWRASXXMS-UHFFFAOYSA-M trimethyl(phenyl)azanium;bromide Chemical compound [Br-].C[N+](C)(C)C1=CC=CC=C1 GNMJFQWRASXXMS-UHFFFAOYSA-M 0.000 description 1
- MQAYPFVXSPHGJM-UHFFFAOYSA-M trimethyl(phenyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)C1=CC=CC=C1 MQAYPFVXSPHGJM-UHFFFAOYSA-M 0.000 description 1
- KKLAORVGAKUOPZ-UHFFFAOYSA-M trimethyl(phenyl)azanium;iodide Chemical compound [I-].C[N+](C)(C)C1=CC=CC=C1 KKLAORVGAKUOPZ-UHFFFAOYSA-M 0.000 description 1
- FCGQIZKUTMUWDC-UHFFFAOYSA-M trimethyl(propyl)azanium;bromide Chemical compound [Br-].CCC[N+](C)(C)C FCGQIZKUTMUWDC-UHFFFAOYSA-M 0.000 description 1
- CEYYIKYYFSTQRU-UHFFFAOYSA-M trimethyl(tetradecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)C CEYYIKYYFSTQRU-UHFFFAOYSA-M 0.000 description 1
- ARMLJSXXXFXSLQ-UHFFFAOYSA-L trimethyl-[10-(trimethylazaniumyl)decyl]azanium;diiodide Chemical compound [I-].[I-].C[N+](C)(C)CCCCCCCCCC[N+](C)(C)C ARMLJSXXXFXSLQ-UHFFFAOYSA-L 0.000 description 1
- RRHXZLALVWBDKH-UHFFFAOYSA-M trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)OCC[N+](C)(C)C RRHXZLALVWBDKH-UHFFFAOYSA-M 0.000 description 1
- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 1
- KPFRXMSETZXGKJ-UHFFFAOYSA-M trimethyl-[3-(trifluoromethyl)phenyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)C1=CC=CC(C(F)(F)F)=C1 KPFRXMSETZXGKJ-UHFFFAOYSA-M 0.000 description 1
- VKZIUXSJJSEBAK-UHFFFAOYSA-M trimethyl-[3-(trifluoromethyl)phenyl]azanium;iodide Chemical compound [I-].C[N+](C)(C)C1=CC=CC(C(F)(F)F)=C1 VKZIUXSJJSEBAK-UHFFFAOYSA-M 0.000 description 1
- FAPSXSAPXXJTOU-UHFFFAOYSA-L trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;dibromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C FAPSXSAPXXJTOU-UHFFFAOYSA-L 0.000 description 1
- PYIHTIJNCRKDBV-UHFFFAOYSA-L trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;dichloride Chemical compound [Cl-].[Cl-].C[N+](C)(C)CCCCCC[N+](C)(C)C PYIHTIJNCRKDBV-UHFFFAOYSA-L 0.000 description 1
- GTFSUBIVRHGESQ-UHFFFAOYSA-M trimethyl-[[2-(trimethylsilylmethyl)phenyl]methyl]azanium;iodide Chemical compound [I-].C[N+](C)(C)CC1=CC=CC=C1C[Si](C)(C)C GTFSUBIVRHGESQ-UHFFFAOYSA-M 0.000 description 1
- AISMNBXOJRHCIA-UHFFFAOYSA-N trimethylazanium;bromide Chemical compound Br.CN(C)C AISMNBXOJRHCIA-UHFFFAOYSA-N 0.000 description 1
- CURCMGVZNYCRNY-UHFFFAOYSA-N trimethylazanium;iodide Chemical compound I.CN(C)C CURCMGVZNYCRNY-UHFFFAOYSA-N 0.000 description 1
- HADKRTWCOYPCPH-UHFFFAOYSA-M trimethylphenylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C1=CC=CC=C1 HADKRTWCOYPCPH-UHFFFAOYSA-M 0.000 description 1
- PRXNKYBFWAWBNZ-UHFFFAOYSA-N trimethylphenylammonium tribromide Chemical compound Br[Br-]Br.C[N+](C)(C)C1=CC=CC=C1 PRXNKYBFWAWBNZ-UHFFFAOYSA-N 0.000 description 1
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical group C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 description 1
- GZKLCETYSGSMRA-UHFFFAOYSA-N trioctadecyl borate Chemical compound CCCCCCCCCCCCCCCCCCOB(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC GZKLCETYSGSMRA-UHFFFAOYSA-N 0.000 description 1
- DTBRTYHFHGNZFX-UHFFFAOYSA-N trioctyl borate Chemical compound CCCCCCCCOB(OCCCCCCCC)OCCCCCCCC DTBRTYHFHGNZFX-UHFFFAOYSA-N 0.000 description 1
- MDCWDBMBZLORER-UHFFFAOYSA-N triphenyl borate Chemical compound C=1C=CC=CC=1OB(OC=1C=CC=CC=1)OC1=CC=CC=C1 MDCWDBMBZLORER-UHFFFAOYSA-N 0.000 description 1
- DWYCJWXMZGVGJV-UHFFFAOYSA-M triphenyl(3-phenylmethoxypropyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)CCCOCC1=CC=CC=C1 DWYCJWXMZGVGJV-UHFFFAOYSA-M 0.000 description 1
- NHDIQVFFNDKAQU-UHFFFAOYSA-N tripropan-2-yl borate Chemical compound CC(C)OB(OC(C)C)OC(C)C NHDIQVFFNDKAQU-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- IJGSGCGKAAXRSC-UHFFFAOYSA-M tris(2-hydroxyethyl)-methylazanium;hydroxide Chemical compound [OH-].OCC[N+](C)(CCO)CCO IJGSGCGKAAXRSC-UHFFFAOYSA-M 0.000 description 1
- RTMBXAOPKJNOGZ-UHFFFAOYSA-N tris(2-methylphenyl) borate Chemical compound CC1=CC=CC=C1OB(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C RTMBXAOPKJNOGZ-UHFFFAOYSA-N 0.000 description 1
- WAXLMVCEFHKADZ-UHFFFAOYSA-N tris-decyl borate Chemical compound CCCCCCCCCCOB(OCCCCCCCCCC)OCCCCCCCCCC WAXLMVCEFHKADZ-UHFFFAOYSA-N 0.000 description 1
- WCTAGTRAWPDFQO-UHFFFAOYSA-K trisodium;hydrogen carbonate;carbonate Chemical compound [Na+].[Na+].[Na+].OC([O-])=O.[O-]C([O-])=O WCTAGTRAWPDFQO-UHFFFAOYSA-K 0.000 description 1
- WTBVYJWHTHPPKB-UHFFFAOYSA-N tritetradecyl borate Chemical compound CCCCCCCCCCCCCCOB(OCCCCCCCCCCCCCC)OCCCCCCCCCCCCCC WTBVYJWHTHPPKB-UHFFFAOYSA-N 0.000 description 1
- QFKMMXYLAPZKIB-UHFFFAOYSA-N undecan-1-amine Chemical compound CCCCCCCCCCCN QFKMMXYLAPZKIB-UHFFFAOYSA-N 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229940074411 xylene Drugs 0.000 description 1
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
Abstract
Description
m1は0又は1を表し、m2は1から4の整数を表し、
A1及びA3は各々独立して、1,2−フェニレン、ナフタレン−1,2−ジイル、ナフタレン−2,3−ジイル、ナフタレン−2,8−ジイル、ナフタレン−1,8−ジイル、ナフタレン−1,7−ジイル、シクロヘキサン−1,2−ジイル、1,2−シクロヘキセニレン、デカヒドロナフタレン−1,2−ジイル、デカヒドロナフタレン−1,8−ジイル、デカヒドロナフタレン−2,3−ジイル、デカヒドロナフタレン−1,7−ジイル、デカヒドロナフタレン−2,8−ジイル、インダン−1,7−ジイル又はインダン−1,2−ジイルを表すが、これらの基は無置換又は1つ以上のLによって置換されても良く、これらの環構造における1つ以上の=CH−は=N−に置換されても良く、若しくはこれらの環構造における1つ以上の連続しない−CH2−は各々独立して−NH−、−O−又は−S−に置換されても良く、
A2は、1,4−フェニレン、ナフタレン−1,4−ジイル、ナフタレン−2,6−ジイル、シクロヘキサン−1,4−ジイル、1,4−シクロヘキセニレン、ビシクロ[2.2.2]オクタン−1,4−ジイル、スピロ[3.3]ヘプタン−2,6−ジイル、デカヒドロナフタレン−2,6−ジイル、1,2,3,4−テトラヒドロナフタレン−2,6−ジイル、インダン−2,5−ジイル、チオフェン−2,5−ジイル又はフルオレン−2,7−ジイルを表すが、これらの基は無置換又は1つ以上のLによって置換されても良く、これらの環構造における1つ以上の=CH−は=N−に置換されても良く、若しくはこれらの基における1つ以上の連続しない−CH2−は各々独立して−NH−、−O−又は−S−に置換されても良く、m2が2〜4を表しA2が複数存在する場合それらは同一であっても異なっていてもよく、
Z1及びZ2は各々独立して、単結合、−O−、−S−、−OCH2−、−CH2O−、−CO−、−COO−、−OCO−、−CO−S−、−S−CO−、−O−CO−O−、−CO−NH−、−NH−CO−、−SCH2−、−CH2S−、−CF2O−、−OCF2−、−CF2S−、−SCF2−、−(C(Y1)2)n1−、−CH=CH−COO−、−CH=CH−OCO−、−COO−CH=CH−、−OCO−CH=CH−、−COO−CH2CH2−、−OCO−CH2CH2−、−CH2CH2−COO−、−CH2CH2−OCO−、−COO−CH2−、−OCO−CH2−、−CH2−COO−、−CH2−OCO−、−CY1=CY1−又は−C≡C−を表し(式中、Y1は水素原子、炭素原子数1から12のアルキル基、フッ素原子、塩素原子又はシアノ基を表し、n1は1から6の整数を表すが、Y1が複数存在する場合それらは同一であっても異なっていてもよい。)、m2が2〜4を表しZ2が複数存在する場合それらは同一であっても異なっていてもよく、
前記LはP−Sp−で表される基、水素原子、フッ素原子、塩素原子、臭素原子、ヨウ素原子、ペンタフルオロスルフラニル基、ニトロ基、シアノ基、ヒドロキシル基、−N(Y3)2、−Si(Y3)3、1個の−CH2−又は隣接していない2個以上の−CH2−が各々独立して−O−、−S−、−CO−、−COO−、−OCO−、−OCO−O−に置き換えられても良い炭素原子数1から20の直鎖状又は分岐状アルキル基(式中、Y3はP−Sp−で表される基、水素原子、フッ素原子、塩素原子、臭素原子、ヨウ素原子、ペンタフルオロスルフラニル基、ニトロ基、シアノ基、ヒドロキシル基、炭素原子数1から20の直鎖状又は分岐状アルキル基を表すが、Y3が複数存在する場合それらは同一であっても異なっていてもよい。)を表し、Lが複数存在する場合にはそれらは同一であっても異なっていてもよく、
前記Spは、スペーサー基又は単結合を表すが、Spが複数存在する場合それらは同一であっても異なっていてもよく、前記Pは、重合性基を表すが、Pが複数存在する場合それらは同一であっても異なっていてもよい。)で表される重合性化合物、当該重合性化合物を含有する重合性組成物、当該重合性化合物を含有する液晶組成物、当該重合性化合物を用いた光学素子及び当該重合性化合物を含有する液晶組成物を用いた光学素子を提供する。
一般式(Ih)で表される化合物として、下記一般式(Il)で表される化合物がさらにより好ましく、一般式(Ii)で表される化合物として、下記一般式(Im)で表される化合物がさらにより好ましく、一般式(Ij)で表される化合物として、下記一般式(In)で表される化合物がさらにより好ましい。
一般式(Il)、一般式(Im)、及び一般式(In)においてSpが単結合であることがより好ましい。
(製法1)下記式(S−10)で表される化合物の製造
(製法2)下記式(S−14)で表される化合物の製造
、テトラブチルアンモニウムジブロモクロリド、テトラブチルアンモニウムジブロモヨージド、テトラブチルアンモニウムジクロロアウラート、テトラブチルアンモニウムジクロロブロミド、テトラブチルアンモニウムジフルオロトリフェニルシリカート、テトラブチルアンモニウムジフルオロトリフェニルスズ、テトラブチルアンモニウム三フッ化二水素、テトラブチルアンモニウムジヨードアウラート、テトラブチルアンモニウムヘキサフルオロホスファート、テトラブチルアンモニウム硫酸水素塩、過塩素酸テトラブチルアンモニウム、過レニウム酸テトラブチルアンモニウム、テトラブチルアンモニウムホスファート、テトラブチルアンモニウムp−ニトロフェノキシド、テトラブチルアンモニウムサリチラート、テトラブチルアンモニウムテトラフルオロボラート、テトラブチルアンモニウムテトラフェニルボラート、テトラブチルアンモニウムチオシアナート、テトラブチルアンモニウムトリブロミド、テトラブチルアンモニウムトリフルオロメタンスルホナート、テトラブチルアンモニウムトリヨージド、3−(テトラデシルジメチルアンモニオ)プロパンスルホナート、テトラエチルアンモニウムボロヒドリド、過塩素酸テトラエチルアンモニウム、テトラエチルアンモニウムp−トルエンスルホナート、テトラエチルアンモニウムテトラフルオロボラート、テトラエチルアンモニウムトリフルオロメタンスルホナート、テトラメチルアンモニウムアセタート、テトラメチルアンモニウムボロヒドリド、テトラメチルアンモニウムヘキサフルオロホスファート、テトラメチルアンモニウム硫酸水素塩、過塩素酸テトラメチルアンモニウム、テトラメチルアンモニウムp−トルエンスルホナート、テトラメチルアンモニウムスルファート、テトラメチルアンモニウムテトラフルオロボラート、テトラメチルアンモニウムトリアセトキシボロヒドリド、テトラプロピルアンモニウムペルルテナート、トリエチルメチルアンモニウムテトラフルオロボラート、トリメチルフェニルアンモニウムトリブロミド、N,N−ビス(3−D−グルコンアミドプロピル)コルアミド[BIGCHAP]、N,N−ビス(3−D−グルコンアミドプロピル)デオキシコルアミド[Deoxy−BIGCHAP]、NIKKOL BL−9EX[ポリオキシエチレン(9)ラウリルエーテル]、オクタノイル−N−メチルグルカミド[MEGA−8]、ノナノイル−N−メチルグルカミド[MEGA−9]、デカノイル−N−メチルグルカミド[MEGA−10]、ポリオキシエチレン(8)オクチルフェニルエーテル[Triton X−114]、ポリオキシエチレン(9)オクチルフェニルエーテル[NP−40]、ポリオキシエチレン(10)オクチルフェニルエーテル[Triton X−100]、ポリオキシエチレン(20)ソルビタンモノラウラート[Tween 20]、ポリオキシエチレン(20)ソルビタンモノパルミタート[Tween 40]、ポリオキシエチレン(20)ソルビタンモノステアラート[Tween 60]、ポリオキシエチレン(20)ソルビタンモノオレアート[Tween 80]、ポリオキシエチレンソルビタントリオレアート[Tween 85]、ポリオキシエチレン(20)ソルビタントリオレアート、ポリオキシエチレン(23)ラウリルエーテル[Brij35]、ポリオキシエチレン(20)セチルエーテル[Brij58]、ドデシル−β−D−マルトピラノシド、ヘプチル−β−D−チオグルコピラニシド、オクチル−β−D−チオグルコピラニシド、ノニル−β−D−チオマルトシド、IGELPAL CA−630、Digitonin、Saponin,from Soybeans、3−[(3−コラミドプロピル)ジメチルアンモニオ]−2−ヒドロキシ−1−プロパンスルホナート[CHAPSO]、3−[(3−コラミドプロピル)ジメチルアンモニオ]−1−プロパンスルホナート[CHAPS]、ヘプタデカフルオロ−1−オクタンスルホン酸アンモニウム、ペンタデカフルオロオクタン酸アンモニウム、ヘプタデカフルオロオクタンスルホン酸、ヘプタデカフルオロ−1−オクタンスルホン酸リチウム、ペンタデカフルオロオクタン酸、ヘプタデカフルオロ−1−オクタンスルホン酸カリウム、3−(ヘキサデシルジメチルアンモニオ)プロパンスルホナート、コール酸ナトリウム、ラウリン酸ナトリウム、ミリスチン酸ナトリウム、N−ラウロイルサルコシンナトリウム、オレイン酸ナトリウム、パルミチン酸ナトリウム、ステアリン酸ナトリウム、スルホコハク酸ビス(2−エチルヘキシル)ナトリウム、ドデセン−1LAS、5−スルホイソフタル酸ジメチルナトリウム、1−ドデカンスルホン酸ナトリウム、ドデシルベンゼンスルホン酸ナトリウム、1−ヘキサデカンスルホン酸ナトリウム、1−オクタデカンスルホン酸ナトリウム、1−ペンタデカンスルホン酸ナトリウム、1−テトラデカンスルホン酸ナトリウム、1−トリデカンスルホン酸ナトリウム、リン酸モノドデシルナトリウム、リン酸モノドデシルナトリウム(モノ、ジナトリウム混合物)、ドデシル硫酸ナトリウム、ヘキサデシル硫酸ナトリウム、ベンゼトニウムクロリド、ヘキサデシルピリジニウムクロリド、1−ドデシルピリジニウムクロリド、ヘキサデシルピリジニウムブロミド、ヘキサデシルピリジニウムクロリド、モノミリスチン、モノパルミチン、モノステアリン、ポリエチレングリコールモノステアラート、ポリエチレングリコールモノステアラート(パルミタート、ステアラート混合物)、ソルビタンモノラウラート[Span 20]、ソルビタンモノパルミタート[Span 40]、ソルビタンモノステアラート[Span 60]、ソルビタンモノオレアート[Span 80]、ソルビタンセスキオレアート[Span 83]、ソルビタントリオレアート[Span 85]、ジエチレングリコールモノドデシルエーテル、エチレングリコールモノドデシルエーテル、ポリエチレングリコールモノセチルエーテル、ポリエチレングリコールモノドデシルエーテル、ポリエチレングリコールモノ−4−オクチルフェニルエーテル、テトラエチルグリコールモノドデシルエーテル、トリエチレングリコールモノドデシルエーテル等が挙げられる。反応条件として、例えば、実験化学講座(日本化学会編、丸善株式会社発行)、Organic Syntheses(A John Wiley & Sons,Inc.,Publication)、Beilstein Handbook of Organic Chemistry(Beilstein−Institut fuer Literatur der Organischen Chemie、Springer−Verlag Berlin and Heidelberg GmbH & Co.K)、Fiesers’ Reagents for Organic Synthesis(John Wiley & Sons,Inc.)等の文献若しくはSciFinder又はReaxys等のデータベースに挙げられている条件が使用可能である。
(製法3)下記式(S−29)で表される化合物の製造
−1−フェニルエトキシカルボニル基、2−(2−ピリジル)アミノ−1−フェニルエトキシカルボニル基、2−[N−メチル−N−(2−ピリジル)]アミノ−1−フェニルエトキシカルボニル基、フェナシルオキシカルボニル基、3’,5’−ジメトキシベンゾインオキシカルボニル基、ベンジルチオキシカルボニル基、ジメチルチオカルボニル基、N−フェニルアミノカルボニル基、N−メチル−N−(o−ニトロフェニル)アミノカルボニル基が挙げられる。
(a)トランス−1,4−シクロへキシレン基(この基中に存在する1個のメチレン基又は隣接していない2個以上のメチレン基は−O−又は−S−に置き換えられてもよい)、
(b)1,4−フェニレン基(この基中に存在する1個の−CH=又は隣接していない2個以上の−CH=は窒素原子に置き換えられてもよい)及び、
(c)1,4−シクロヘキセニレン基、1,4−ビシクロ[2.2.2]オクチレン基、ピペリジン−2,5−ジイル基、ナフタレン−2,6−ジイル基、1,2,3,4−テトラヒドロナフタレン−2,6−ジイル基及びデカヒドロナフタレン−2,6−ジイル基
からなる群より選ばれる基を表し、
上記の基(a)、基(b)又は基(c)に含まれる水素原子はそれぞれシアノ基、フッ素原子、トリフルオロメチル基、トリフルオロメトキシ基又は塩素原子で置換されていても良く、Z3、Z4、Z5、Z6、Z7及びZ8は各々独立して単結合、−COO−、−OCO−、−CH2CH2−、−(CH2)4−、−OCH2−、−CH2O−、−OCF2−、−CF2O−又は−C≡C−を表し、A4、A5、A6、A7、A8、A9、Z3、Z4、Z5、Z6、Z7及び/又はZ8が複数存在する場合は、それらは同一でも良く異なっていても良く、L1、L2、L3、L4及びL5は各々独立して水素原子、トリフルオロメチル基、トリフルオロメトキシ基、フッ素原子又は塩素原子を表すが、L1及びL2が同時に水素原子を表すことは無く、L3、L4及びL5が同時に水素原子を表すことは無く、m4、m5、m6及びm7は各々独立して、0、1、2又は3を表すが、m4+m5及びm6+m7は4以下である。一般式(II−1)においては、一般式(II−2)で表される化合物を除く。)で表される化合物。
(a)トランス−1,4−シクロへキシレン基(この基中に存在する1個のメチレン基又は隣接していない2個以上のメチレン基は−O−又は−S−に置き換えられてもよい)、
(b)1,4−フェニレン基(この基中に存在する1個の−CH=又は隣接していない2個以上の−CH=は窒素原子に置き換えられてもよい)、3−フルオロ−1,4−フェニレン基、3,5−ジフルオロ−1,4−フェニレン基及び、
(c)1,4−シクロヘキセニレン基、1,4−ビシクロ[2.2.2]オクチレン基、ピペリジン−2,5−ジイル基、ナフタレン−2,6−ジイル基、1,2,3,4−テトラヒドロナフタレン−2,6−ジイル基及びデカヒドロナフタレン−2,6−ジイル基からなる群より選ばれる基を表し、
上記の基(a)、基(b)又は基(c)に含まれる水素原子はそれぞれシアノ基、フッ素原子、トリフルオロメチル基、トリフルオロメトキシ基又は塩素原子で置換されていても良く、Z9、Z10、Z11、Z12、Z13及びZ14は各々独立して単結合、−COO−、−OCO−、−CH2CH2−、−(CH2)4−、−OCH2−、−CH2O−、−OCF2−、−CF2O−又は−C≡C−を表し、A11、A12、A14、A15、Z9、Z11、Z12及び/又はZ14が複数存在する場合は、それらは同一でも良く異なっていても良く、L6、L7、L8、L9及びL10は各々独立して水素原子又はフッ素原子を表し、Y1及びY2は各々独立して水素原子、フッ素原子、塩素原子、シアノ基、チオシアナト基、トリフルオロメトキシ基、トリフルオロメチル基、2,2,2−トリフルオロエチル基又はジフルオロメトキシ基を表し、L6、L7又はY1のうち少なくともひとつはフッ素原子、塩素原子、シアノ基、チオシアナト基、トリフルオロメトキシ基、トリフルオロメチル基、2,2,2−トリフルオロエチル基、又はジフルオロメトキシ基を表すか、A10又はA12に含まれる水素原子のうち少なくともひとつはシアノ基、フッ素原子、トリフルオロメチル基、トリフルオロメトキシ基又は塩素原子を表し、L8、L9、L10又はY2のうち少なくともひとつはフッ素原子、塩素原子、シアノ基、チオシアナト基、トリフルオロメトキシ基、トリフルオロメチル基、2,2,2−トリフルオロエチル基、ジフルオロメトキシ基を表すか、A13、A14又はA15に含まれる水素原子のうち少なくともひとつはシアノ基、フッ素原子、トリフルオロメチル基、トリフルオロメトキシ基又は塩素原子を表し、m8、m9、m10及びm11は各々独立して、0、1又は2を表す。一般式(III−1)においては、一般式(III−2)で表される化合物を除く。)で表される化合物。
(a)トランス−1,4−シクロへキシレン基(この基中に存在する1個のメチレン基又は隣接していない2個以上のメチレン基は−O−又は−S−に置き換えられてもよい)、(b)1,4−フェニレン基(1個の−CH=又は隣接していない2個以上の−CH=は窒素原子に置き換えられても良い。)、3−フルオロ−1,4−フェニレン基及び3,5−ジフルオロ−1,4−フェニレン基並びに
(c)1,4−シクロヘキセニレン基、1,4−ビシクロ(2.2.2)オクチレン基、ピペリジン−2,5−ジイル基、ナフタレン−2,6−ジイル基、デカヒドロナフタレン−2,6−ジイル基及び1,2,3,4−テトラヒドロナフタレン−2,6−ジイル基
からなる群より選ばれる基を表し、m12は0又は1を表し、Z15及びZ16は各々独立して単結合、−CH2CH2−、−(CH2)4−、−OCH2−、−CH2O−、−OCF2−、−CF2O−、−CF2CF2−、−COO−、−OCO−、−CH=CH−、−CF=CF−、−CH=N−、−N=CH−、−CH=N−N=CH−又は−C≡C−を表し、Z16及び/又はA18が複数存在する場合は、それらは同一でも良く異なっていても良い。一般式(IV)においては、一般式(II−1)、一般式(II−2)、一般式(III−1)、及び、一般式(III−2)で表される化合物を除く。)で表される化合物。
(実施例1)式(I−1)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,750,690cm−1.
LRMS:392
HRMS:392.13
(実施例2)式(I−2)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,750,690cm−1.
LRMS:406
HRMS:406.14
(実施例3)式(I−3)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,750,690cm−1.
LRMS:428
HRMS:428.13
(実施例4)式(I−4)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,750,690cm−1.
LRMS:442
HRMS:442.14
(実施例5)式(I−5)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,750,690cm−1.
LRMS:468
HRMS:468.16
(実施例6)式(I−6)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,750,690cm−1.
1H NMR(CDCl3)δ 1.92(s,3H),2.08(s,3H),2.09(s,3H),5.65(m,1H),5.79(m,2H),6.19(m,1H),6.38(m,2H),7.09(d,1H),7.15(dd,1H),7.21(m,2H),7.49(m,3H),7.60(m,2H),7.64(m,2H)ppm.
13C NMR(CDCl3)δ 18.3,18.4,18.4,116.6,119.5,121.9,126.9,127.4,127.7,127.7,128.0,129.4,131.1,131.8,135.3,135.5,135.7,135.8,138.2,139.3,148.1,150.4,150.4,165.3,165.5,165.9ppm.
LRMS:482
HRMS:482.17
(実施例7)式(I−7)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,810,750,690cm−1.
LRMS:420
HRMS:420.16
(実施例8)式(I−8)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,810,750,690cm−1.
LRMS:448
HRMS:448.19
(実施例9)式(I−9)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,750,690cm−1.
LRMS:504
HRMS:504.25
(実施例10)式(I−10)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,810,750,690cm−1.
1H NMR(CDCl3)δ 1.87(s,3H),2.08(s,3H),2.11(s,3H),5.60(m,1H),5.81(m,2H),6.15(m,1H),6.39(m,1H),6.42(m,1H),7.12(d,1H),7.17(dd,1H),7.28(dd,1H),7.54(d,1H),7.56(dd,1H),7.61(d,1H),7.81(d,1H),7.86(d,1H),7.89(d,1H)ppm.
13C NMR(CDCl3)δ 18.3,18.4,18.5,116.7,118.4,119.6,121.6,127.5,127.5,127.7,127.8,127.9,129.6,131.2,131.4,132.1,132.9,134.2,135.2,135.6,135.8,148.3,148.8,150.5,165.3,165.5,166.1ppm.
LRMS:456
HRMS:456.16
(実施例11)式(I−11)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,810,750,690cm−1.
LRMS:604
HRMS:604.27
(実施例12)式(I−12)で表される化合物の製造
IR:3060−3030,2975−2920,1725,1630,1200,1160,1130,810,750,690cm−1.
LRMS:500
HRMS:500.15
実施例1から実施例12記載の方法と同様の方法によって式(I−13)から式(I−40)
(実施例13〜24、比較例1〜3)
本願発明の重合性化合物(I−1)から重合性化合物(I−12)並びに特許文献1の実施例1記載の比較化合物1、特許文献2の<例1>記載の比較化合物2及び特許文献3の例6記載の比較化合物3を評価対象の重合性化合物とした。
母体液晶(X1)に、評価対象の重合性化合物を5%添加し溶解させ重合性液晶組成物を調製した。評価対象の化合物の溶解性を、調製した液晶組成物を−30℃で60日間保存した後の析出物の有無によって評価した。目視によって析出物が見られた場合、析出物を濾過しガスクロマトグラフィー(GC)により分析を行った。結果を下記表に示す。
《表示素子の作製》
母体液晶(X1)に、評価対象の重合性化合物を0.3%添加し溶解させ重合性液晶組成物を調製し、評価対象の重合性液晶組成物とした。この評価対象の重合性液晶組成物を、セルギャップ3.5μmでホメオトロピック配向を誘起するポリイミド配向膜を塗布したITO付きセルに真空注入法で注入した。周波数1kHzで1.8Vの矩形波を印加しながら、高圧水銀灯を用いて320nm以上のUVを10mW/cm2で600秒間照射することにより、評価対象のPSA型垂直配向性液晶表示素子(XI)を作製した。下記表に評価対象の重合性化合物と液晶表示素子との関係を示す。
重合性化合物の重合のしやすさを評価するために、上記液晶表示素子を分解し取り出した液晶組成物を液体クロマトグラフ(HPLC)を用いて分析し、未硬化の重合性化合物の量を測定した。未硬化の重合性化合物の量が多いほど、重合性化合物が重合しにくいことを意図している。結果を下記表に示す。
《プレチルト角の安定性の評価》
上記液晶表示素子のプレチルト角の安定性について評価を行うために、作製した表示素子を70℃で24時間加熱し、加熱前と加熱後のプレチルト角をクリスタルローテーション法により評価した。結果を下記表に示す。
《焼き付きの評価》
上記液晶表示素子の焼き付きの生じにくさを比較するために、70℃で7.5Vの電圧を印加し経過時間ごとに目視によって評価を行った。目視によって焼き付きが無ければ○、僅かに焼き付きが見られる場合は△、焼き付きが強く見られる場合は×とした。結果を下記表に示す。
(実施例25〜36、比較例4〜6)
本願発明の化合物(I−1)から化合物(I−12)並びに上記比較化合物1、比較化合物2及び比較化合物3を評価対象の化合物とした。
母体液晶(X2)に、評価対象の重合性化合物を5%添加し溶解させ重合性液晶組成物を調製した。評価対象の重合性化合物の溶解性を、調製した液晶組成物を−30℃で60日間保存した後の析出物の有無によって評価した。目視によって析出物が見られた場合、析出物を濾過しGCにより分析を行った。結果を下記表に示す。
《表示素子の作製》
母体液晶(X2)に、評価対象の重合性化合物を0.3%添加し溶解させ重合性液晶組成物を調製し、評価対象の重合性液晶組成物とした。この評価対象の重合性液晶組成物を、セルギャップ3.5μmのホモジニアス配向を誘起するポリイミド配向膜を塗布したITOからなる櫛歯電極を有するセルに真空注入法で注入した。このセルに1.6Vの電圧を印可しながら320nm以下の紫外線をカットするフィルターを介して、高圧水銀灯により液晶セルに紫外線を照射した。セル表面の照射強度が10mW/cm2となるように調整して600秒間照射して、重合性液晶組成物中の重合性化合物を重合させた水平配向性液晶表示素子(XII)を得た。下記表に評価対象の重合性化合物と液晶表示素子との関係を示す。
重合性化合物の重合のしやすさを評価するために、上記液晶表示素子を分解し取り出した液晶組成物をHPLCを用いて分析し、未硬化の重合性化合物の量を測定した。未硬化の重合性化合物の量が多いほど、重合性化合物が重合しにくいことを意図している。結果を下記表に示す。
《焼き付きの評価》
上記液晶表示素子の焼き付きの生じにくさを比較するために、70℃で7.5Vの電圧を印加し経過時間ごとに目視によって評価を行った。目視によって焼き付きが無ければ○、僅かに焼き付きが見られる場合は△、焼き付きが強く見られる場合は×とした。結果を下記表に示す。
(実施例37〜48、比較例7〜9)
本願発明の化合物(I−1)から化合物(I−12)並びに上記比較化合物1、比較化合物2及び比較化合物3を評価対象の化合物とした。
Claims (14)
- 一般式(I)
m1は0又は1を表し、m2は1から4の整数を表し、
A1及びA3は各々独立して、1,2−フェニレン、ナフタレン−1,2−ジイル、ナフタレン−2,3−ジイル、ナフタレン−2,8−ジイル、ナフタレン−1,8−ジイル、ナフタレン−1,7−ジイル、シクロヘキサン−1,2−ジイル、1,2−シクロヘキセニレン、デカヒドロナフタレン−1,2−ジイル、デカヒドロナフタレン−1,8−ジイル、デカヒドロナフタレン−2,3−ジイル、デカヒドロナフタレン−1,7−ジイル、デカヒドロナフタレン−2,8−ジイル、インダン−1,7−ジイル又はインダン−1,2−ジイルを表すが、これらの基は無置換又は1つ以上のLによって置換されても良く、これらの環構造における1つ以上の=CH−は=N−に置換されても良く、若しくはこれらの環構造における1つ以上の連続しない−CH2−は各々独立して−NH−、−O−又は−S−に置換されても良く、
A2は、1,4−フェニレン、ナフタレン−1,4−ジイル、ナフタレン−2,6−ジイル、シクロヘキサン−1,4−ジイル、1,4−シクロヘキセニレン、ビシクロ[2.2.2]オクタン−1,4−ジイル、スピロ[3.3]ヘプタン−2,6−ジイル、デカヒドロナフタレン−2,6−ジイル、1,2,3,4−テトラヒドロナフタレン−2,6−ジイル、インダン−2,5−ジイル、チオフェン−2,5−ジイル又はフルオレン−2,7−ジイルを表すが、これらの基は無置換又は1つ以上のLによって置換されても良く、これらの環構造における1つ以上の=CH−は=N−に置換されても良く、若しくはこれらの基における1つ以上の連続しない−CH2−は各々独立して−NH−、−O−又は−S−に置換されても良く、m2が2〜4を表しA2が複数存在する場合それらは同一であっても異なっていてもよく、
Z1及びZ2は各々独立して、単結合、−O−、−S−、−OCH2−、−CH2O−、−CO−、−COO−、−OCO−、−CO−S−、−S−CO−、−O−CO−O−、−CO−NH−、−NH−CO−、−SCH2−、−CH2S−、−CF2O−、−OCF2−、−CF2S−、−SCF2−、−(C(Y1)2)n1−、−CH=CH−COO−、−CH=CH−OCO−、−COO−CH=CH−、−OCO−CH=CH−、−COO−CH2CH2−、−OCO−CH2CH2−、−CH2CH2−COO−、−CH2CH2−OCO−、−COO−CH2−、−OCO−CH2−、−CH2−COO−、−CH2−OCO−、−CY1=CY1−又は−C≡C−を表し(式中、Y1は水素原子、炭素原子数1から12のアルキル基、フッ素原子、塩素原子又はシアノ基を表し、n1は1から6の整数を表すが、Y1が複数存在する場合それらは同一であっても異なっていてもよい。)、m2が2〜4を表しZ2が複数存在する場合それらは同一であっても異なっていてもよく、
前記LはP−Sp−で表される基、水素原子、フッ素原子、塩素原子、臭素原子、ヨウ素原子、ペンタフルオロスルフラニル基、ニトロ基、シアノ基、ヒドロキシル基、−N(Y3)2、−Si(Y3)3、1個の−CH2−又は隣接していない2個以上の−CH2−が各々独立して−O−、−S−、−CO−、−COO−、−OCO−、−OCO−O−に置き換えられても良い炭素原子数1から20の直鎖状又は分岐状アルキル基(式中、Y3はP−Sp−で表される基、水素原子、フッ素原子、塩素原子、臭素原子、ヨウ素原子、ペンタフルオロスルフラニル基、ニトロ基、シアノ基、ヒドロキシル基、炭素原子数1から20の直鎖状又は分岐状アルキル基を表すが、Y3が複数存在する場合それらは同一であっても異なっていてもよい。)を表し、Lが複数存在する場合にはそれらは同一であっても異なっていてもよく、
前記Spは、スペーサー基又は単結合を表すが、Spが複数存在する場合それらは同一であっても異なっていてもよく、前記Pは、重合性基を表すが、Pが複数存在する場合それらは同一であっても異なっていてもよい。)で表される重合性化合物。 - Spが、1個の−CH2−又は隣接していない2個以上の−CH2−が各々独立して−O−、−COO−、−OCO−又は−OCO−O−に置き換えられても良い炭素原子数1から20のアルキレン基又は単結合を表す請求項1又は2記載の重合性化合物。
- A3が、無置換であるか又は1つ以上のLによって置換されても良い1,2−フェニレン、ナフタレン−1,2−ジイル又はナフタレン−2,3−ジイルを表す請求項1から請求項3のいずれか1項に記載の重合性化合物。
- 請求項1から請求項5のいずれか一項に記載の重合性化合物を含有する重合性組成物。
- 1種又は2種以上の請求項1から請求項5のいずれか一項に記載の重合性化合物及び一般式(II−1)及び一般式(II−2)
(a)トランス−1,4−シクロへキシレン基(この基中に存在する1個のメチレン基又は隣接していない2個以上のメチレン基は−O−又は−S−に置き換えられてもよい)、
(b)1,4−フェニレン基(この基中に存在する1個の−CH=又は隣接していない2個以上の−CH=は窒素原子に置き換えられてもよい)及び、
(c)1,4−シクロヘキセニレン基、1,4−ビシクロ[2.2.2]オクチレン基、ピペリジン−2,5−ジイル基、ナフタレン−2,6−ジイル基、1,2,3,4−テトラヒドロナフタレン−2,6−ジイル基及びデカヒドロナフタレン−2,6−ジイル基からなる群より選ばれる基を表し、
上記の基(a)、基(b)又は基(c)に含まれる水素原子はそれぞれシアノ基、フッ素原子、トリフルオロメチル基、トリフルオロメトキシ基又は塩素原子で置換されていても良く、Z3、Z4、Z5、Z6、Z7及びZ8は各々独立して単結合、−COO−、−OCO−、−CH2CH2−、−(CH2)4−、−OCH2−、−CH2O−、−OCF2−、−CF2O−又は−C≡C−を表し、A5、A6、A8、A9、Z3、Z5、Z6、及び/又はZ8が複数存在する場合は、それらは同一でも良く異なっていても良く、L1、L2、L3、L4及びL5は各々独立して水素原子、トリフルオロメチル基、トリフルオロメトキシ基、フッ素原子又は塩素原子を表すが、L1及びL2が同時に水素原子を表すことは無く、L3、L4及びL5が同時に水素原子を表すことは無く 、m4、m5、m6及びm7は各々独立して、0、1、2又は3を表すが、m4+m5及びm6+m7は4以下である。一般式(II−1)においては、一般式(II−2)で表される化合物を除く。)で表される群から選ばれる1種又は2種以上の化合物を含有する液晶組成物。 - 1種又は2種以上の請求項1から請求項5のいずれか一項に記載の重合性化合物及び一般式(III−1)及び一般式(III−2)
(a)トランス−1,4−シクロへキシレン基(この基中に存在する1個のメチレン基又は隣接していない2個以上のメチレン基は−O−又は−S−に置き換えられてもよい)、
(b)1,4−フェニレン基(この基中に存在する1個の−CH=又は隣接していない2個以上の−CH=は窒素原子に置き換えられてもよい)、3−フルオロ−1,4−フェニレン基、3,5−ジフルオロ−1,4−フェニレン基及び、
(c)1,4−シクロヘキセニレン基、1,4−ビシクロ[2.2.2]オクチレン基、ピペリジン−2,5−ジイル基、ナフタレン−2,6−ジイル基、1,2,3,4−テトラヒドロナフタレン−2,6−ジイル基及びデカヒドロナフタレン−2,6−ジイル基からなる群より選ばれる基を表し、
上記の基(a)、基(b)又は基(c)に含まれる水素原子はそれぞれシアノ基、フッ素原子、トリフルオロメチル基、トリフルオロメトキシ基又は塩素原子で置換されていても良く、
Z9、Z10、Z11、Z12、Z13及びZ14は各々独立して単結合、−COO−、−OCO−、−CH2CH2−、−(CH2)4−、−OCH2−、−CH2O−、−OCF2−、−CF2O−又は−C≡C−を表し、A11、A12、A14、A15、Z9、Z11、Z12及び/又はZ14が複数存在する場合は、それらは同一でも良く異なっていても良く、L6、L7、L8、L9及びL10は各々独立して水素原子又はフッ素原子を表し、Y1及びY2は各々独立して水素原子、フッ素原子、塩素原子、シアノ基、チオシアナト基、トリフルオロメトキシ基、トリフルオロメチル基、2,2,2−トリフルオロエチル基又はジフルオロメトキシ基を表し、L6、L7又はY1が同時に水素原子を表すことは無く、又はA10又はA12に含まれる水素原子のうち少なくとも1つはシアノ基、フッ素原子、トリフルオロメチル基、トリフルオロメトキシ基又は塩素原子を表し、L8、L9、L10又はY2が同時に水素原子を表すことは無く、又はA13、A14又はA15に含まれる水素原子のうち少なくとも1つはシアノ基、フッ素原子、トリフルオロメチル基、トリフルオロメトキシ基又は塩素原子を表し、m8、m9、m10及びm11は各々独立して、0、1又は2を表す。一般式(III−1)においては、一般式(III−2)で表される化合物を除く。)で表される群から選ばれる1種又は2種以上の化合物を含有する液晶組成物。 - 一般式(IV)
(a)トランス−1,4−シクロへキシレン基(この基中に存在する1個のメチレン基又は隣接していない2個以上のメチレン基は−O−又は−S−に置き換えられてもよい)、(b)1,4−フェニレン基(1個の−CH=又は隣接していない2個以上の−CH=は窒素原子に置き換えられても良い。)、3−フルオロ−1,4−フェニレン基及び3,5−ジフルオロ−1,4−フェニレン基並びに
(c)1,4−シクロヘキセニレン基、1,4−ビシクロ(2.2.2)オクチレン基、ピペリジン−2,5−ジイル基、ナフタレン−2,6−ジイル基、デカヒドロナフタレン−2,6−ジイル基及び1,2,3,4−テトラヒドロナフタレン−2,6−ジイル基
からなる群より選ばれる基を表し、m12は0又は1を表し、Z15及びZ16は各々独立して単結合、−CH2CH2−、−(CH2)4−、−OCH2−、−CH2O−、−OCF2−、−CF2O−、−CF2CF2−、−COO−、−OCO−、−CH=CH−、−CF=CF−、−CH=N−、−N=CH−、−CH=N−N=CH−又は−C≡C−を表し、Z16及び/又はA18が複数存在する場合は、それらは同一でも異なっていても良い。一般式(IV)においては、一般式(II−1)、一般式(II−2)、一般式(III−1)及び、一般式(III−2)で表される化合物を除く。)で表される群から選ばれる1種又は2種以上の化合物を含有する請求項7又は請求項8に記載の液晶組成物。 - 請求項1から請求項5のいずれか一項に記載の重合性化合物を用いた光学素子。
- 請求項7から請求項9のいずれか一項に記載の液晶組成物を用いた光学素子。
- 光を透過する層と電極とを備えた、2枚の基板を有し、これらの基板の間に請求項6記載の組成物を硬化してなる硬化物、又は請求項7から請求項9のいずれか一項に記載の液晶組成物を硬化してなる硬化物を含んでなる光学素子。
- PS(ポリマー安定化)型用又はPSA(ポリマー維持配向)型用である請求項10から請求項12のいずれか一項に記載の光学素子。
- 請求項1から請求項5のいずれか一項に記載の化合物又は当該化合物を硬化してなる硬化物を使用した液晶材料、樹脂、樹脂添加剤、オイル、オイルフィルター、油脂、インキ、医薬品、化粧品、洗剤、農薬及び食品並びにそれらを使用した製品。
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Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6274987A (ja) * | 1985-09-28 | 1987-04-06 | メルク・パテント・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング | 液晶相を有する重合体化合物 |
JPH01299559A (ja) * | 1988-05-27 | 1989-12-04 | Nippon Contact Lens Kk | 眼科用レンズ |
JPH02180909A (ja) * | 1988-12-30 | 1990-07-13 | Ipposha Oil Ind Co Ltd | ベンゾフェノン系化合物及びその単独重合物或いは共重合物 |
JPH04186340A (ja) * | 1990-11-21 | 1992-07-03 | Fuji Photo Film Co Ltd | 感光感熱記録材料 |
JPH05310840A (ja) * | 1992-05-07 | 1993-11-22 | Mitsubishi Kasei Corp | 高分子液晶化合物および液晶素子 |
JP2003307720A (ja) * | 2002-04-16 | 2003-10-31 | Fujitsu Ltd | 液晶表示装置 |
JP2007503487A (ja) * | 2003-08-25 | 2007-02-22 | 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 ハフトング | メソゲン性化合物、電気光学ディスプレイ用媒体および電気光学ディスプレイ |
CN101186577A (zh) * | 2006-11-15 | 2008-05-28 | 西北工业大学 | 具有反应特性的液晶单体及其制备方法 |
JP2010536894A (ja) * | 2007-08-30 | 2010-12-02 | 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 | 液晶ディスプレイ |
WO2011036080A1 (fr) * | 2009-09-23 | 2011-03-31 | Polymage | Materiau composite utilisant un elastomere mesomorphe et son procede de fabrication |
JP2011515543A (ja) * | 2008-03-25 | 2011-05-19 | 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 | 液晶ディスプレイ |
JP2012523486A (ja) * | 2009-04-14 | 2012-10-04 | コミトブ,ラヒェザー | Lcd配向膜のためのマレイミド−n−ビニルラクタム系側基ポリマー |
CN102888229A (zh) * | 2012-09-21 | 2013-01-23 | 深圳市华星光电技术有限公司 | 液晶介质混合物及使用其的液晶显示器 |
WO2013017467A1 (en) * | 2011-08-02 | 2013-02-07 | Rolic Ag | Photoaligning material |
WO2013161576A1 (ja) * | 2012-04-24 | 2013-10-31 | Jnc株式会社 | 重合性基を4つ有する化合物、液晶組成物および液晶表示素子 |
-
2013
- 2013-03-29 JP JP2013072526A patent/JP6102423B2/ja active Active
Patent Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6274987A (ja) * | 1985-09-28 | 1987-04-06 | メルク・パテント・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング | 液晶相を有する重合体化合物 |
JPH01299559A (ja) * | 1988-05-27 | 1989-12-04 | Nippon Contact Lens Kk | 眼科用レンズ |
JPH02180909A (ja) * | 1988-12-30 | 1990-07-13 | Ipposha Oil Ind Co Ltd | ベンゾフェノン系化合物及びその単独重合物或いは共重合物 |
JPH04186340A (ja) * | 1990-11-21 | 1992-07-03 | Fuji Photo Film Co Ltd | 感光感熱記録材料 |
JPH05310840A (ja) * | 1992-05-07 | 1993-11-22 | Mitsubishi Kasei Corp | 高分子液晶化合物および液晶素子 |
JP2003307720A (ja) * | 2002-04-16 | 2003-10-31 | Fujitsu Ltd | 液晶表示装置 |
JP2007503487A (ja) * | 2003-08-25 | 2007-02-22 | 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 ハフトング | メソゲン性化合物、電気光学ディスプレイ用媒体および電気光学ディスプレイ |
CN101186577A (zh) * | 2006-11-15 | 2008-05-28 | 西北工业大学 | 具有反应特性的液晶单体及其制备方法 |
JP2010536894A (ja) * | 2007-08-30 | 2010-12-02 | 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 | 液晶ディスプレイ |
JP2011515543A (ja) * | 2008-03-25 | 2011-05-19 | 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 | 液晶ディスプレイ |
JP2012523486A (ja) * | 2009-04-14 | 2012-10-04 | コミトブ,ラヒェザー | Lcd配向膜のためのマレイミド−n−ビニルラクタム系側基ポリマー |
WO2011036080A1 (fr) * | 2009-09-23 | 2011-03-31 | Polymage | Materiau composite utilisant un elastomere mesomorphe et son procede de fabrication |
WO2013017467A1 (en) * | 2011-08-02 | 2013-02-07 | Rolic Ag | Photoaligning material |
WO2013161576A1 (ja) * | 2012-04-24 | 2013-10-31 | Jnc株式会社 | 重合性基を4つ有する化合物、液晶組成物および液晶表示素子 |
CN102888229A (zh) * | 2012-09-21 | 2013-01-23 | 深圳市华星光电技术有限公司 | 液晶介质混合物及使用其的液晶显示器 |
Non-Patent Citations (7)
Title |
---|
COLLOIDS AND SURFACES, A:PHYSICOCHEMICAL AND ENGINEERING ASPECTS, vol. 181(1-3), JPN6016039554, 2001, pages 303 - 313, ISSN: 0003426641 * |
JOURNAL OF MATERIALS CHEMISTRY, vol. 3(3), JPN6016039552, 1993, pages 241 - 245, ISSN: 0003426639 * |
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 128(41), JPN6016039555, 2006, pages 13376 - 13377, ISSN: 0003426642 * |
LIQUID CRYSTALS, vol. 40(4), JPN6016039553, 28 January 2013 (2013-01-28), pages 546 - 554, ISSN: 0003426640 * |
MACROMOLECULAR CHEMISTRY AND PHYSICS, vol. 199(2), JPN6016039549, 1998, pages 207 - 213, ISSN: 0003426636 * |
MOLECULAR CRYSTALS AND LIQUID CRYSTALS SCIENCE AND TECHNOLOGY, SECTION A:MOLECULAR CRYSTALS AND LIQU, vol. 241, JPN6016039551, 1994, pages 119 - 129, ISSN: 0003426638 * |
MOLECULAR CRYSTALS AND LIQUID CRYSTALS SCIENCE AND TECHNOLOGY, SECTION A:MOLECULAR CRYSTALS AND LIQU, vol. 258, JPN6016039550, 1995, pages 51 - 60, ISSN: 0003426637 * |
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US9938229B2 (en) | 2014-07-30 | 2018-04-10 | Merck Patent Gmbh | Polymerisable compounds and the use thereof in liquid-crystal displays |
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EP2980062A3 (en) * | 2014-07-30 | 2016-04-06 | Merck Patent GmbH | Polymerisable compounds and the use thereof in liquid-crystal displays |
EP3124465A1 (en) * | 2014-07-30 | 2017-02-01 | Merck Patent GmbH | Polymerisable compounds and the use thereof in liquid-crystal displays |
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TWI704173B (zh) * | 2015-01-14 | 2020-09-11 | 日商捷恩智股份有限公司 | 具有聚合性基的化合物、液晶組成物及液晶顯示元件 |
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CN107108453A (zh) * | 2015-01-14 | 2017-08-29 | 捷恩智株式会社 | 具有聚合性基的化合物、液晶组合物及液晶显示元件 |
WO2016114093A1 (ja) * | 2015-01-14 | 2016-07-21 | Jnc株式会社 | 重合性基を有する化合物、液晶組成物および液晶表示素子 |
JP2020097566A (ja) * | 2015-01-14 | 2020-06-25 | Jnc株式会社 | 重合性基を有する化合物、液晶組成物および液晶表示素子 |
EP3656757A1 (en) * | 2015-01-14 | 2020-05-27 | JNC Corporation | Compound having polymerizable group, liquid crystal composition and liquid crystal display element |
JPWO2016114093A1 (ja) * | 2015-01-14 | 2017-11-02 | Jnc株式会社 | 重合性基を有する化合物、液晶組成物および液晶表示素子 |
US10479940B2 (en) | 2015-04-23 | 2019-11-19 | Jnc Corporation | Liquid crystal composition and liquid crystal display device |
WO2016170948A1 (ja) * | 2015-04-23 | 2016-10-27 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
CN106242973A (zh) * | 2015-06-09 | 2016-12-21 | 默克专利股份有限公司 | 可聚合化合物及其在液晶显示器中的用途 |
JP2018532869A (ja) * | 2015-09-15 | 2018-11-08 | 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 | ホメオトロピック配向を有する液晶媒体 |
CN108026448A (zh) * | 2015-09-15 | 2018-05-11 | 默克专利股份有限公司 | 具有垂面配向的液晶介质 |
CN108026019A (zh) * | 2015-09-15 | 2018-05-11 | 捷恩智株式会社 | 聚合性极性化合物、液晶组合物及液晶显示元件 |
CN108026448B (zh) * | 2015-09-15 | 2022-01-04 | 默克专利股份有限公司 | 具有垂面配向的液晶介质 |
JP2017132704A (ja) * | 2016-01-26 | 2017-08-03 | 日本化薬株式会社 | エポキシ樹脂、およびその組成物 |
WO2017217243A1 (ja) * | 2016-06-16 | 2017-12-21 | Dic株式会社 | エポキシ(メタ)アクリレート樹脂及びレジスト部材 |
JPWO2017217243A1 (ja) * | 2016-06-16 | 2018-06-21 | Dic株式会社 | エポキシ(メタ)アクリレート樹脂及びレジスト部材 |
JP2018070546A (ja) * | 2016-11-02 | 2018-05-10 | Dic株式会社 | エステル結合を有するビスフェノール誘導体 |
CN110382666A (zh) * | 2017-03-09 | 2019-10-25 | 默克专利股份有限公司 | 可聚合化合物及其于液晶显示器中的用途 |
US11718791B2 (en) | 2017-03-09 | 2023-08-08 | Merck Patent Gmbh | Polymerisable compounds and the use thereof in liquid-crystal displays |
CN110382666B (zh) * | 2017-03-09 | 2023-05-26 | 默克专利股份有限公司 | 可聚合化合物及其于液晶显示器中的用途 |
JPWO2018168721A1 (ja) * | 2017-03-17 | 2020-01-16 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
WO2018168721A1 (ja) * | 2017-03-17 | 2018-09-20 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
JP2019073589A (ja) * | 2017-10-13 | 2019-05-16 | Jnc株式会社 | 液晶組成物および液晶表示素子 |
US11015122B2 (en) * | 2017-12-20 | 2021-05-25 | Shijiazhuang Chengzhi Yonghua Display Material Co., Ltd. | Liquid crystal composition and liquid crystal display element |
CN109943347A (zh) * | 2017-12-20 | 2019-06-28 | 石家庄诚志永华显示材料有限公司 | 液晶组合物及液晶显示元件 |
CN112004914A (zh) * | 2018-04-23 | 2020-11-27 | 默克专利股份有限公司 | 液晶混合物及液晶显示器 |
JP2019218335A (ja) * | 2018-05-30 | 2019-12-26 | 住友化学株式会社 | 化合物、樹脂、レジスト組成物及びレジストパターンの製造方法 |
JP2020002065A (ja) * | 2018-06-28 | 2020-01-09 | Dic株式会社 | 重合性化合物並びにそれを使用した液晶組成物及び液晶表示素子 |
JPWO2020116555A1 (ja) * | 2018-12-06 | 2021-02-15 | Dic株式会社 | 液晶組成物及び液晶表示素子 |
WO2020116555A1 (ja) * | 2018-12-06 | 2020-06-11 | Dic株式会社 | 液晶組成物及び液晶表示素子 |
JP2021017475A (ja) * | 2019-07-18 | 2021-02-15 | Dic株式会社 | 液晶組成物及び液晶表示素子 |
JP2021017520A (ja) * | 2019-07-23 | 2021-02-15 | Dic株式会社 | ネマチック液晶組成物、液晶表示素子、及びその製造方法 |
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