CN118108620A - Hydroxyalkylamide compounds - Google Patents
Hydroxyalkylamide compounds Download PDFInfo
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- CN118108620A CN118108620A CN202410236258.5A CN202410236258A CN118108620A CN 118108620 A CN118108620 A CN 118108620A CN 202410236258 A CN202410236258 A CN 202410236258A CN 118108620 A CN118108620 A CN 118108620A
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- liquid crystal
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 115
- 101100322581 Caenorhabditis elegans add-1 gene Proteins 0.000 claims abstract description 14
- 101100322583 Caenorhabditis elegans add-2 gene Proteins 0.000 claims abstract description 13
- 239000004973 liquid crystal related substance Substances 0.000 description 219
- 239000010408 film Substances 0.000 description 128
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 94
- 239000000758 substrate Substances 0.000 description 75
- 239000003795 chemical substances by application Substances 0.000 description 61
- 125000004432 carbon atom Chemical group C* 0.000 description 56
- 238000000034 method Methods 0.000 description 55
- 150000004985 diamines Chemical class 0.000 description 51
- 229920000642 polymer Polymers 0.000 description 50
- 229920005575 poly(amic acid) Polymers 0.000 description 49
- 229920001721 polyimide Polymers 0.000 description 46
- 239000000243 solution Substances 0.000 description 44
- 239000002904 solvent Substances 0.000 description 39
- 239000004642 Polyimide Substances 0.000 description 31
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 26
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 26
- -1 t-butoxycarbonyl Chemical group 0.000 description 26
- 238000006243 chemical reaction Methods 0.000 description 25
- 230000015572 biosynthetic process Effects 0.000 description 21
- 150000002430 hydrocarbons Chemical class 0.000 description 21
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 20
- 238000003786 synthesis reaction Methods 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
- 125000000962 organic group Chemical group 0.000 description 19
- 125000000217 alkyl group Chemical group 0.000 description 18
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 17
- 238000011156 evaluation Methods 0.000 description 17
- ZFPGARUNNKGOBB-UHFFFAOYSA-N 1-Ethyl-2-pyrrolidinone Chemical compound CCN1CCCC1=O ZFPGARUNNKGOBB-UHFFFAOYSA-N 0.000 description 16
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 16
- 239000000203 mixture Substances 0.000 description 16
- 239000000565 sealant Substances 0.000 description 16
- 125000006158 tetracarboxylic acid group Chemical group 0.000 description 16
- 239000002253 acid Substances 0.000 description 15
- 239000011248 coating agent Substances 0.000 description 15
- 238000000576 coating method Methods 0.000 description 15
- 210000002858 crystal cell Anatomy 0.000 description 15
- 239000010410 layer Substances 0.000 description 15
- 150000002148 esters Chemical class 0.000 description 14
- 238000010438 heat treatment Methods 0.000 description 14
- 239000002243 precursor Substances 0.000 description 14
- 229910052757 nitrogen Inorganic materials 0.000 description 13
- 125000004433 nitrogen atom Chemical group N* 0.000 description 13
- RWNUSVWFHDHRCJ-UHFFFAOYSA-N 1-butoxypropan-2-ol Chemical compound CCCCOCC(C)O RWNUSVWFHDHRCJ-UHFFFAOYSA-N 0.000 description 12
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 125000003118 aryl group Chemical group 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 10
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 10
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 10
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 9
- 230000001747 exhibiting effect Effects 0.000 description 9
- 229930195733 hydrocarbon Natural products 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 230000005855 radiation Effects 0.000 description 9
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 8
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
- 210000004027 cell Anatomy 0.000 description 8
- UYAAVKFHBMJOJZ-UHFFFAOYSA-N diimidazo[1,3-b:1',3'-e]pyrazine-5,10-dione Chemical compound O=C1C2=CN=CN2C(=O)C2=CN=CN12 UYAAVKFHBMJOJZ-UHFFFAOYSA-N 0.000 description 8
- 238000010304 firing Methods 0.000 description 8
- 238000005227 gel permeation chromatography Methods 0.000 description 8
- 239000011521 glass Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 8
- 229940116423 propylene glycol diacetate Drugs 0.000 description 8
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 7
- 238000001035 drying Methods 0.000 description 7
- 229910052731 fluorine Inorganic materials 0.000 description 7
- 125000001153 fluoro group Chemical group F* 0.000 description 7
- 125000005843 halogen group Chemical group 0.000 description 7
- 125000005842 heteroatom Chemical group 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- 239000004952 Polyamide Substances 0.000 description 6
- 229910052581 Si3N4 Inorganic materials 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 229920002647 polyamide Polymers 0.000 description 6
- 238000007789 sealing Methods 0.000 description 6
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 5
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 5
- 238000005160 1H NMR spectroscopy Methods 0.000 description 5
- VATRWWPJWVCZTA-UHFFFAOYSA-N 3-oxo-n-[2-(trifluoromethyl)phenyl]butanamide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1C(F)(F)F VATRWWPJWVCZTA-UHFFFAOYSA-N 0.000 description 5
- 125000002723 alicyclic group Chemical group 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 239000004305 biphenyl Substances 0.000 description 5
- 235000010290 biphenyl Nutrition 0.000 description 5
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 238000004528 spin coating Methods 0.000 description 5
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 4
- 125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 description 4
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 4
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 150000008065 acid anhydrides Chemical class 0.000 description 4
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- BHXIWUJLHYHGSJ-UHFFFAOYSA-N ethyl 3-ethoxypropanoate Chemical compound CCOCCC(=O)OCC BHXIWUJLHYHGSJ-UHFFFAOYSA-N 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 4
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 238000003825 pressing Methods 0.000 description 4
- 125000006239 protecting group Chemical group 0.000 description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
- 125000006850 spacer group Chemical group 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 125000000304 alkynyl group Chemical group 0.000 description 3
- 150000008064 anhydrides Chemical group 0.000 description 3
- 238000007664 blowing Methods 0.000 description 3
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 229940116333 ethyl lactate Drugs 0.000 description 3
- 125000004428 fluoroalkoxy group Chemical group 0.000 description 3
- 125000003709 fluoroalkyl group Chemical group 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- ZBKFYXZXZJPWNQ-UHFFFAOYSA-N isothiocyanate group Chemical group [N-]=C=S ZBKFYXZXZJPWNQ-UHFFFAOYSA-N 0.000 description 3
- 229940101545 mi-acid Drugs 0.000 description 3
- 125000001624 naphthyl group Chemical group 0.000 description 3
- 125000003566 oxetanyl group Chemical group 0.000 description 3
- 125000000466 oxiranyl group Chemical group 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- QNLZIZAQLLYXTC-UHFFFAOYSA-N 1,2-dimethylnaphthalene Chemical compound C1=CC=CC2=C(C)C(C)=CC=C21 QNLZIZAQLLYXTC-UHFFFAOYSA-N 0.000 description 2
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 2
- ITWBWJFEJCHKSN-UHFFFAOYSA-N 1,4,7-triazonane Chemical compound C1CNCCNCCN1 ITWBWJFEJCHKSN-UHFFFAOYSA-N 0.000 description 2
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- IBXNCJKFFQIKKY-UHFFFAOYSA-N 1-pentyne Chemical compound CCCC#C IBXNCJKFFQIKKY-UHFFFAOYSA-N 0.000 description 2
- LDQMZKBIBRAZEA-UHFFFAOYSA-N 2,4-diaminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C(N)=C1 LDQMZKBIBRAZEA-UHFFFAOYSA-N 0.000 description 2
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 description 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
- LVYXPOCADCXMLP-UHFFFAOYSA-N 3-butoxy-n,n-dimethylpropanamide Chemical compound CCCCOCCC(=O)N(C)C LVYXPOCADCXMLP-UHFFFAOYSA-N 0.000 description 2
- LBVMWHCOFMFPEG-UHFFFAOYSA-N 3-methoxy-n,n-dimethylpropanamide Chemical compound COCCC(=O)N(C)C LBVMWHCOFMFPEG-UHFFFAOYSA-N 0.000 description 2
- KQIKKETXZQDHGE-FOCLMDBBSA-N 4,4'-diaminoazobenzene Chemical compound C1=CC(N)=CC=C1\N=N\C1=CC=C(N)C=C1 KQIKKETXZQDHGE-FOCLMDBBSA-N 0.000 description 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- HXQPUEQDBSPXTE-UHFFFAOYSA-N Diisobutylcarbinol Chemical compound CC(C)CC(O)CC(C)C HXQPUEQDBSPXTE-UHFFFAOYSA-N 0.000 description 2
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 239000004988 Nematic liquid crystal Substances 0.000 description 2
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 229920002396 Polyurea Polymers 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 125000004018 acid anhydride group Chemical group 0.000 description 2
- ORILYTVJVMAKLC-UHFFFAOYSA-N adamantane Chemical compound C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 2
- 239000002318 adhesion promoter Substances 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 2
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 2
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/20—Carboxylic acid amides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C08L79/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
-
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- 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
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- G02F1/13—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 for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
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Abstract
The present invention relates to a hydroxyalkylamide compound. The compound is represented by the following formula (Add-1) or (Add-2),
Description
The application is a divisional application of the following application:
the invention name is as follows: liquid crystal aligning agent, liquid crystal alignment film and liquid crystal display element.
International application date: 2021, 10 and 4.
International application number: PCT/JP2021/036656.
National application number: 202180076210.7.
Technical Field
The present invention relates to a liquid crystal aligning agent, a liquid crystal alignment film obtained from the liquid crystal aligning agent, and a liquid crystal display element using the liquid crystal alignment film.
Background
Conventionally, a liquid crystal display device has been widely used as a display portion of a personal computer, a smart phone, a mobile phone, a television receiver, or the like. The liquid crystal display device includes, for example: a liquid crystal layer sandwiched between the element substrate and the color filter substrate; a pixel electrode and a common electrode for applying an electric field to the liquid crystal layer; an alignment film for controlling alignment properties of liquid crystal molecules of the liquid crystal layer; and a Thin Film Transistor (TFT) converting an electric signal supplied to the pixel electrode; etc. As a driving method of liquid crystal molecules, there is known: a longitudinal electric field system such as TN (TWISTED NEMATIC: twisted nematic) system and VA (VERTICAL ALIGNMENT: vertical alignment) system; IPS (IN PLANE SWITCHING: in-plane switching) mode, FFS (FRINGE FIELD SWITCHING: fringe field switching) mode, and the like.
Currently, the most industrially used liquid crystal alignment film is produced by performing a so-called rubbing (Rubbing) treatment of rubbing the surface of a film formed on an electrode substrate and made of a polymer represented by polyamic acid and/or polyimide obtained by imidizing the polyamic acid in one direction by using a cloth such as cotton, nylon, or polyester. The rubbing treatment is a simple and industrially useful method with excellent productivity. As an alignment treatment method instead of rubbing treatment, a photo-alignment method is known in which polarized radiation is irradiated to impart alignment ability to liquid crystals. As the photo-alignment method, a method using a photoisomerization reaction is proposed; a method using a photocrosslinking reaction; a method using a photodecomposition reaction, and the like (see non-patent document 1, patent document 1).
In recent years, a large-screen and high-definition liquid crystal television has been mainly used, and in addition, the popularization of small-sized display terminals such as smartphones, tablet PCs, and car navigation has been advanced, and the demand for higher quality of liquid crystal display elements has been further increased than ever before. As reliability tests of liquid crystal display elements for mobile applications such as smartphones and in-vehicle applications such as car navigation, vibration tests of panels are sometimes performed. In the vibration test, it is required that defects such as bright spots do not occur.
In order to secure a display surface as large as possible, a so-called narrowing of the frame is required in which the width of the sealant between substrates for bonding the liquid crystal display element is as narrow as possible. With this narrowing of the frame, a sealant used in manufacturing a liquid crystal display element is applied on a liquid crystal alignment film. Along with this, a liquid crystal alignment film having high adhesion (hereinafter also referred to as sealing adhesion) between the sealant and the liquid crystal alignment film is demanded.
Further, when the alignment characteristic is exhibited by the rubbing treatment, there is a problem in that dust is easily generated due to cutting of the liquid crystal alignment film. When dust is generated, dust adheres to the surface of the liquid crystal alignment film, which causes defective display, and also causes circuit breakdown of the TFT element, which reduces the yield.
In this way, in order to obtain a liquid crystal display element which does not cause defects accompanying vibration test and rubbing treatment and a liquid crystal alignment film having high sealing adhesion, for example, a method of improving the mechanical strength of the liquid crystal alignment film is considered. As a method for improving the mechanical strength of the liquid crystal alignment film, particularly the film strength, a method of adding a crosslinking agent to the liquid crystal alignment agent is exemplified. As a means for solving these problems, a liquid crystal aligning agent containing a specific polyimide component and a specific hydroxyalkylamide compound has been proposed (see patent document 2). Further, regarding the electric characteristics, which are basic characteristics of the liquid crystal alignment film, it is also required to display higher initial characteristics.
Prior art literature
Patent literature
Patent document 1: japanese patent laid-open No. 9-297313
Patent document 2: WO2018/092811
Non-patent literature
Non-patent document 1: "liquid crystal photo-alignment film" wood household hypochondrium, city village, functional material, 1997, 11 month Vol.17, no.11, pages 13-22
Disclosure of Invention
Problems to be solved by the invention
From the studies by the present inventors, the like, it is known that: when the specific hydroxyalkylamide compound described in patent document 2 is added, the film strength of the obtained liquid crystal alignment film is improved, but the anisotropy of the liquid crystal alignment film contributing to the liquid crystal alignment property is reduced.
The contrast of the liquid crystal display element of the liquid crystal alignment film having low anisotropy is deteriorated, and there is a possibility that a ghost (hereinafter, also referred to as AC ghost) may be generated due to long-term alternating current driving. Therefore, a liquid crystal aligning agent having high anisotropy of a liquid crystal alignment film is demanded while improving the film strength of the liquid crystal alignment film.
As described above, an object of the present invention is to provide a liquid crystal aligning agent capable of obtaining a liquid crystal alignment film having high film strength and exhibiting high anisotropy, a liquid crystal alignment film, and a liquid crystal display element having the liquid crystal alignment film.
Solution for solving the problem
The present inventors have conducted intensive studies to solve the above problems, and as a result, have found that the above problems can be solved by using a specific hydroxyalkylamide compound, and have completed the present invention.
The present invention provides a liquid crystal aligning agent, a liquid crystal alignment film obtained from the liquid crystal aligning agent, a liquid crystal display element having the liquid crystal alignment film, and a novel compound used for the liquid crystal aligning agent, wherein the liquid crystal aligning agent is characterized by comprising the following component (A) and component (B).
(A) The components are as follows: a polymer (A) having an ability to orient liquid crystals.
(B) The components are as follows: a hydroxyalkylamide compound (B) represented by the following formula (1).
P—o—W—o—P (1)
In the formula (1), P independently represents a group having a group "×c (=o) -N (R) 2", W represents a partial structure exhibiting liquid crystallinity, R independently represents a group "×cr '2)2 -OH", and R' independently represents a hydrogen atom or a monovalent organic group having 1 to 6 carbon atoms.
In this specification, a bond is expressed in any case. Examples of the halogen atom include: fluorine atom, chlorine atom, bromine atom, iodine atom. Preferred examples of the urethane protecting group include t-butoxycarbonyl and 9-fluorenylmethoxycarbonyl.
Effects of the invention
According to the present invention, a liquid crystal aligning agent capable of obtaining a liquid crystal alignment film having high film strength and exhibiting high anisotropy, the liquid crystal alignment film, and a liquid crystal display element having the liquid crystal alignment film can be obtained. Further, a liquid crystal display element with less display defects is provided. Further, a liquid crystal alignment film excellent in sealing adhesion, voltage holding ratio, and residual image characteristics can be obtained.
The mechanism by which the above-described effects of the present invention are obtained is not necessarily clear, but it is considered that the following is one of the reasons.
That is, it is considered that the residual image characteristic is filled by a portion structure exhibiting liquid crystallinity disposed in the center. In particular, it is considered that the presence of chain hydrocarbons at both ends of the partial structure exhibiting liquid crystallinity greatly contributes to suppression of stretchability inhibition and promotion of the liquid crystallinity expression effect.
Detailed Description
Component (A)
The liquid crystal aligning agent of the present invention contains a polymer having an ability to align liquid crystal, similarly to the known liquid crystal aligning agent, and the polymer is not particularly limited as long as it has an ability to align liquid crystal. The liquid crystal aligning agent of the present invention may contain one kind of the polymer, or may contain two or more kinds.
Examples of the polymer include: polyimide precursors, polyimides as imide compounds of polyimide precursors, acrylic polymers, methacrylic polymers, acrylamide polymers, methacrylamide polymers, polystyrene, polysiloxanes, polyamides, polyesters, polyurethanes, polycarbonates, polyureas, polyphenols (novolak resins), maleimide polymers, polymers into which compounds having an isocyanuric acid skeleton or a triazine skeleton have been introduced.
The following materials are used as raw materials for producing these polymers.
When the polymer is a polyimide precursor such as polyamic acid or polyamic acid ester, or polyimide, at least one tetracarboxylic dianhydride or diamine selected from tetracarboxylic acids or derivatives thereof is used.
When the polymer is a (meth) acrylic polymer, (meth) acrylic acid or a derivative thereof, or (meth) acrylic acid ester or a derivative thereof can be used.
When the polymer is a (meth) acrylamide polymer, there may be mentioned (meth) acrylamide or a derivative thereof.
When the polymer is polystyrene, styrene or a derivative thereof may be mentioned.
In the case where the polymer is polysiloxane, a silane compound having methoxy group or ethoxy group is exemplified.
When the polymer is a polyamide, at least one dicarboxylic acid component selected from dicarboxylic acids and derivatives thereof and a diamine component are exemplified.
When the polymer is a polyester, at least one dicarboxylic acid component and glycol component selected from dicarboxylic acids and derivatives thereof are exemplified.
In the case where the polymer is polyurethane, a compound having isocyanate and a compound having hydroxyl groups are exemplified.
In the case where the polymer is polycarbonate, bisphenol derivatives and phosgene or phosgene equivalents (e.g., trichlorophosgene) or diphenyl carbonate may be mentioned.
When the polymer is polyurea, diisocyanate derivatives and diamine components are exemplified.
When the polymer is a maleimide polymer, a maleimide derivative homopolymer or a copolymer with styrene can be exemplified.
In the case where the polymer is a polymer into which a compound having an isocyanuric acid skeleton or a triazine skeleton is introduced, the compound having an isocyanuric acid skeleton or a triazine skeleton can be exemplified.
< Polyimide-based Polymer >)
Among these, one or more polymers selected from the group consisting of polyimide precursors and polyimides that are imidized as polyimide precursors (hereinafter also referred to as polyimide-based polymers) are preferable from the viewpoints of practicality as a liquid crystal aligning agent, mechanical strength of a coating film, and liquid crystal alignment.
The polyimide polymer can be produced by a known method. For example, a polyamic acid as a polyimide precursor is obtained by polymerizing (polycondensing) a tetracarboxylic acid component composed of a tetracarboxylic dianhydride or a derivative thereof and a diamine component, and a polyimide is obtained by imidizing the polyimide precursor. The derivative of the tetracarboxylic dianhydride includes a tetracarboxylic dihalide, a tetracarboxylic dialkyl ester, and a tetracarboxylic dialkyl ester dihalide.
< Tetracarboxylic acid component >
The polyamide acid as the polyimide precursor may be, for example, a material obtained from a tetracarboxylic acid component containing an aromatic, acyclic aliphatic or alicyclic tetracarboxylic dianhydride or a derivative thereof. The tetracarboxylic dianhydride or its derivative may be used alone or in combination of two or more.
Here, the aromatic tetracarboxylic dianhydride is an acid dianhydride obtained by intramolecular dehydration of four carboxyl groups including at least one carboxyl group bonded to an aromatic ring. The acyclic aliphatic tetracarboxylic dianhydride is an acid dianhydride obtained by intramolecular dehydration of four carboxyl groups bonded to a chain hydrocarbon structure. The aromatic hydrocarbon compound may have an alicyclic structure or an aromatic ring structure in a part thereof, without being composed of only a chain hydrocarbon structure.
The alicyclic tetracarboxylic dianhydride is an acid dianhydride obtained by intramolecular dehydration of four carboxyl groups including at least one carboxyl group bonded to an alicyclic structure. Wherein none of the four carboxyl groups is bonded to an aromatic ring. Further, the structure need not be composed of only an alicyclic structure, and may have a chain hydrocarbon structure or an aromatic ring structure in a part thereof.
Among these, the polyamic acid of the present invention is preferably obtained from a tetracarboxylic acid component containing a tetracarboxylic dianhydride represented by the following formula (2) or a derivative thereof.
(X represents a structure selected from the following formulae (X-1) to (X-13)).
(R 1~R4 each independently represents a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkynyl group having 2 to 6 carbon atoms, a monovalent organic group having 1 to 6 carbon atoms containing a fluorine atom, or a phenyl group R 5 and R 6 each independently represents a hydrogen atom or a methyl group, j and k are integers of 0 or1, A 1 and A 2 each independently represent a single bond, -O-, -CO-, -COO-, phenylene, sulfonyl, or amide group; two A 2 are optionally the same or different; A1 is a bond to one acid anhydride group, and A2 is a bond to the other acid anhydride group).
As preferable specific examples of the tetracarboxylic dianhydride represented by the above formula (2) or a derivative thereof, X is selected from the group consisting of the above formulas (X-1) to (X-8) and (X-10) to (X-13).
Among them, the structure selected from the group consisting of the following formulas (X1-1) to (X1-6) is preferable in the formula (X-1).
(. 1 Is a bond to one anhydride group and. 2 is a bond to the other anhydride group).
As preferable specific examples of the above-mentioned formulae (x-12) and (x-13), the following formulae (x-14) to (x-29) are given. In the formula, "x" indicates a bonding position.
The amount of the tetracarboxylic dianhydride or derivative represented by the formula (2) to be used is preferably 60 to 100 mol%, more preferably 80 to 100 mol%, and even more preferably 90 to 100 mol%, based on 1 mol of the total tetracarboxylic acid component reacted with the diamine component.
< Diamine component >
The diamine component used for producing the polyimide precursor is not particularly limited, and preferably includes at least one diamine selected from the diamines represented by the following formula (3) and the following formula (3A). The diamine component may be used alone or in combination of two or more.
(Y 3 represents a divalent organic group represented by the following formula (O): R independently represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, Y 3a represents a divalent organic group represented by the following formula (a).
(Ar represents a divalent benzene ring, a biphenyl structure or a naphthalene ring; two Ar's are optionally the same or different, the above benzene ring, biphenyl structure or naphthalene ring optionally substituted with monovalent substituent(s) p is an integer of 0 or 1, Q 3 represents a group in which at least a part of the above-mentioned-CH 2 -of- (CH 2)n - (n is an integer of 2 to 18) or the above-mentioned-CH 2)n -is substituted with any one of-O-, -C (=O) -or-O-C (=O) -).
(In the formula (a), a hydrogen atom on the benzene ring is optionally substituted with a halogen atom, an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a fluoroalkyl group having 1 to 10 carbon atoms, a fluoroalkoxy group having 1 to 10 carbon atoms. P is any one aromatic ring selected from a benzene ring or a biphenyl structure, a hydrogen atom on the benzene ring or the biphenyl structure is optionally substituted with a methyl group or a fluorine atom. N is an integer of 0 to 5. When n is an integer of 2 or more, n P independently have the above-mentioned definition).
Examples of the substituent for the benzene ring, biphenyl structure or naphthalene ring in the above formula (O) include: halogen atom, alkyl group having 1 to 10 carbon atoms, alkenyl group having 2 to 10 carbon atoms, alkoxy group having 1 to 10 carbon atoms, fluoroalkyl group having 1 to 10 carbon atoms, fluoroalkenyl group having 2 to 10 carbon atoms, fluoroalkoxy group having 1 to 10 carbon atoms, carboxyl group, hydroxyl group, alkyloxycarbonyl group having 1 to 10 carbon atoms, cyano group, nitro group, etc.
From the viewpoint of improving the liquid crystal alignment, the divalent organic groups represented by the above formula (O) are preferably divalent organic groups represented by the following formulas (O-1) to (O-16).
(In the formula (o-14), two m are each independently defined as above).
From the viewpoint of improving the liquid crystal alignment property, the divalent organic groups represented by the above formula (3 a) are preferably divalent organic groups represented by the following formulas (A-1) to (A-7).
The proportion of the total of at least one diamine selected from the diamines represented by the formulas (3) and (3A) is preferably 1 to 95 mol%, more preferably 1 to 90 mol%, and even more preferably 5 to 90 mol% relative to 1 mol of the diamine component.
The polyimide-based polymer used in the present invention may have at least one nitrogen atom-containing structure (hereinafter, also referred to as a specific nitrogen atom-containing structure) selected from the group consisting of a nitrogen atom-containing heterocyclic ring (excluding an imide ring of polyimide), a secondary amino group, and a tertiary amino group, from the viewpoint of improving the voltage holding ratio of the obtained liquid crystal alignment film. The polyimide-based polymer having a specific nitrogen atom structure can be obtained by using a monomer having a nitrogen atom structure, for example, a diamine having a specific nitrogen atom structure, for at least a part of the raw materials.
Examples of the nitrogen atom-containing heterocyclic ring that the diamine having a specific nitrogen atom-containing structure may have include: pyrrole, imidazole, pyrazole, triazole, pyridine, pyrimidine, pyridazine, pyrazine, indole, benzimidazole, purine, quinoline, isoquinoline, naphthyridine, quinoxaline, phthalazine, triazine, carbazole, acridine, piperidine, piperazine, pyrrolidine, hexamethyleneimine, and the like. Among them, pyridine, pyrimidine, pyrazine, piperidine, piperazine, quinoline, carbazole, or acridine are preferable.
The secondary amino group and the tertiary amino group which the diamine having a specific nitrogen atom structure may have are represented by, for example, the following formula (n).
In the above formula (n), R represents a hydrogen atom or a monovalent hydrocarbon group having 1 to 10 carbon atoms. ".1,".2 "represents a bond to a hydrocarbon group.
Examples of the monovalent hydrocarbon group of R in the above formula (n) include: alkyl groups such as methyl, ethyl, and propyl; cycloalkyl groups such as cyclohexyl; aryl groups such as phenyl and methylphenyl. R is preferably a hydrogen atom or a methyl group.
Specific examples of the diamine having a specific nitrogen atom-containing structure include: 2, 6-diaminopyridine, 3, 4-diaminopyridine, 2, 4-diaminopyrimidine, 3, 6-diaminocarbazole, N-methyl-3, 6-diaminocarbazole, 1, 4-bis- (4-aminophenyl) -piperazine, 3, 6-diaminoacridine, N-ethyl-3, 6-diaminocarbazole, N-phenyl-3, 6-diaminocarbazole, compounds represented by the following formulae (Dp-1) to (Dp-8), and compounds represented by the following formulae (z-1) to (z-18).
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The proportion of diamine having a specific nitrogen atom-containing structure to be used is preferably 1 mol% or more, more preferably 2 mol% or more, based on the total amount of diamine used for synthesis, from the viewpoint of improving the voltage holding ratio of the liquid crystal display element. The use ratio is preferably 90 mol% or less, more preferably 80 mol% or less.
The polyimide-based polymer used in the present invention may contain a diamine other than the diamine described above. Examples of other diamines are listed below, but the present invention is not limited thereto.
There may be mentioned: diamines having 6 to 30 carbon atoms other than D and having a group "-N (D) - (D represent urethane-based protecting groups)" in the molecule; diamines having a photo-alignment group such as 4,4' -diaminoazobenzene and a diamine represented by the following formula (d T-1)~(dT -3); 3,3' -diaminodiphenylmethane, 3,4' -diaminodiphenylmethane, 4' -diaminobenzophenone, 1, 4-bis (4-aminobenzyl) benzene, diamines represented by the following formulae (3 i-1) to (3 i-5), 2, 4-diaminophenol, 3, 5-diaminobenzyl alcohol, 2, 4-diaminobenzyl alcohol, 4, 6-diaminoresorcinol; diamines having a carboxyl group, such as 2, 4-diaminobenzoic acid, 2, 5-diaminobenzoic acid, 3, 5-diaminobenzoic acid, and diamine compounds represented by the following formulas (3 b-1) to (3 b-4); 4- (2- (methylamino) ethyl) aniline, 4- (2-aminoethyl) aniline, 4' -diaminodiphenylmethane, 4' -diaminobenzophenone, 4' -diaminodiphenyl ether, 4' -diaminoanilide 4,4' -diaminoazobenzene, 1- (4-aminophenyl) -1, 3-trimethyl-1H-indan-5-amine, 1- (4-aminophenyl) -2, 3-dihydro-1, 3-trimethyl-1H-inden-6-amine; diamines having urea bonds such as diamines represented by the following formulas (h-1) to (h-3); diamines having an amide bond represented by the following formulas (h-4) to (h-6); diamines having a photopolymerizable group at the terminal such as 2- (2, 4-diaminophenoxy) ethyl methacrylate and 2, 4-diamino-N, N-diallylaniline; diamines having a steroid skeleton such as cholesteryl-3, 5-diaminobenzene, cholesteryloxy-2, 4-diaminobenzene, 3, 5-diaminobenzoate cholesteryl ester, 3, 5-diaminobenzoate lanostanyl ester, and 3, 6-bis (4-aminobenzoyloxy) cholestane; diamines represented by the following formulas (V-1) to (V-6); diamines having a siloxane bond such as 1, 3-bis (3-aminopropyl) -tetramethyldisiloxane; diamines having an oxazoline structure such as the following formulae (Ox-1) to (Ox-2); and diamines in which two amino groups described in International publication No. 2018/117239 are bonded to groups represented by any one of the formulas (Y-1) to (Y-167).
(In the formulae (3 i-1) to (3 i-3), two n are optionally the same or different).
(In the formula (3 b-1), A 1 represents a single bond 、-CH2-、-C2H4-、-C(CH3)2-、-CF2-、-C(CF3)2-、-O-、-CO-、-NH-、-N(CH3)-、-CONH-、-NHCO-、-CH2O-、-OCH2-、-COO-、-OCO-、-CON(CH3)- or-N (CH 3) CO-, m1 and m2 each independently represent an integer of 0 to 4, and m1+m2 represents an integer of 1 to 4 in the formula (3 b-2), m3 and m4 each independently represent an integer of 1 to 5 in the formula (3 b-3), A 2 represents a linear or branched alkyl group having 1 to 5 carbon atoms, and m5 represents an integer of 1 to 5 in the formula (3 b-4), A 3 and A 4 each independently represent a single bond 、-CH2-、-C2H4-、-C(CH3)2-、-CF2-、-C(CF3)2-、-O-、-CO-、-NH-、-N(CH3)-、-CONH-、-NHCO-、-CH2O-、-OCH2-、-COO-、-OCO-、-CON(CH3)- or-N (CH 3) CO-, and m6 represents an integer of 1 to 4.
X v5 represents-O-; -CH 2O-、-CH2 OCO-, -COO-; X v5 represents-O-, -CH 2O-、-CH2 OCO-, -COO-; or-OCO-. X a represents a single bond 、-O-、-NH-、-O-(CH2)m-O-、-C(CH3)2-、-CO-、-(CH2)m-、-SO2-、-O-C(CH3)2-、-CO-(CH2)m-、-NH-(CH2)m-、-SO2-(CH2)m-、-CONH-(CH2)m-、-CONH-(CH2)m-NHCO-、-COO-(CH2)m-OCO-、-CONH-、-NH-(CH2)m-NH-、 or-SO 2-(CH2)m-SO2 - (wherein, m represents an integer of 1 to 6), R v1~Rv4、R1a~R1b each independently represents an alkyl group having 1 to 20 carbon atoms, an alkoxy group having 1 to 20 carbon atoms or an alkoxyalkyl group having 2 to 20 carbon atoms in formula (V-6), two k are optionally the same or different.
Examples of the diamine having 6 to 30 carbon atoms other than D and having the group "-N (D) - (D represent urethane-based protecting groups)" in the molecule include compounds represented by the following formulas (5-1) to (5-10).
(Boc represents Boc.)
Component (B)
The liquid crystal aligning agent of the present invention is characterized by comprising a hydroxyalkylamide compound (B) represented by the following formula (1).
P—o—W—o—P (1)
In the formula (1), P independently represents a group having a group of ". Times. -C (=O) -N (R) 2", W represents a partial structure exhibiting liquid crystallinity, R independently represents a group of "- (CR '2)2 -OH", R' independently represents a hydrogen atom or a monovalent organic group having 1 to 6 carbon atoms).
As a partial structure exhibiting liquid crystallinity in W, a mesogenic structure is exemplified. Examples of the mesogenic structure include a structure represented by the following formula (w).
(Ar 1 and Ar 2 are each independently a substituted or unsubstituted phenylene group or a cyclohexylene group, X 1 is a single bond, -CO-, -COO-, -c=c-, -c≡c-, -n=n-, or-CONR 1-(R1 is a hydrogen atom or a monovalent organic group). n is an integer of 1 to 3. Ar 1、X1 has the above definition independently of each other when n is 2 or 3).
In the above formula (w), X 1 is preferably a single bond or-COO-. Examples of the monovalent organic group of R 1 include an alkyl group having 1 to 6 carbon atoms and a protecting group. Specific examples of the protecting group include: t-butoxycarbonyl, benzyloxycarbonyl, 1-dimethyl-2-haloethylcarbonyl, allyloxycarbonyl, and the like.
The substituents of the ring portions of Ar 1 and Ar 2 are preferably an alkyl group having 1 to 5 carbon atoms or a halogen atom, more preferably a methyl group or a fluorine atom.
Preferable specific examples of the partial structure represented by the above formula (w) include, for example: 4,4 '-biphenylene, 4' -dicyclohexylene, p-terphenyl, groups represented by the following formulae (1-1) to (1-4), groups having a methyl group or a fluorine atom in the ring portion of these groups, and the like.
P in the above formula (1) represents a group having a group "×c (=o) -N (R) 2". Specific examples of P include the group "×c (=o) -N (R) 2" or the group "×a-C (=o) -N (R) 2". A represents a divalent organic group having 1 to 30 carbon atoms. Examples of the divalent organic group in A include a divalent hydrocarbon group, a divalent heteroatom-containing group containing a heteroatom-containing group between carbon-carbon bonds of the hydrocarbon group, and a divalent organic group in which some or all of hydrogen atoms contained in the divalent hydrocarbon group and the divalent heteroatom-containing group are substituted with substituents.
Examples of the divalent hydrocarbon group in a of the group "x-a-C (=o) -N (R) 2" include a divalent hydrocarbon group obtained by removing two hydrogen atoms from the following hydrocarbon: alkanes such as methane, ethane, propane, butane, etc.; olefins such as ethylene, propylene, butene, and pentene; chain hydrocarbon having 1 to 30 carbon atoms such as acetylene, propyne, butyne, pentyne and the like; cycloalkanes such as cyclopropane, cyclobutane, cyclopentane, cyclohexane, norbornane, and adamantane; alicyclic hydrocarbons having 3 to 30 carbon atoms such as cycloolefins including cyclopropene, cyclobutene, cyclopentene, cyclohexene and norbornene; aromatic hydrocarbons having 6 to 30 carbon atoms such as benzene, toluene, xylene, mesitylene, naphthalene, methylnaphthalene, dimethylnaphthalene, and anthracene.
The group "a-C (=o) -N (R) 2" is preferably a divalent hydrocarbon group having 1 to 30 carbon atoms, more preferably a divalent hydrocarbon group obtained by removing two hydrogen atoms from a divalent chain hydrocarbon having 1 to 30 carbon atoms or an aromatic hydrocarbon having 6 to 30 carbon atoms.
The divalent chain hydrocarbon having 1 to 30 carbon atoms is preferably a divalent chain hydrocarbon having 2 to 30 carbon atoms, and more preferably a divalent chain hydrocarbon having 2 to 16 carbon atoms.
Examples of the monovalent organic group having 1 to 6 carbon atoms in R 'in the group "- (CR' 2)2 -OH" include an alkyl group having 1 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkynyl group having 2 to 6 carbon atoms, a heteroatom-containing group having a heteroatom between carbon-carbon bonds of these groups, and a group in which some or all of hydrogen atoms in the alkyl group, alkenyl group, alkynyl group and heteroatom-containing group are substituted with a substituent.
Among the above groups "x-a-C (=o) -N (R) 2", a group "- (CR' 2)2 -OH"), examples of the group having a hetero atom include a group having at least one selected from the group consisting of an oxygen atom, a nitrogen atom, a silicon atom, a phosphorus atom and a sulfur atom, and examples thereof include-O-, -NR- (R represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms), -CO-, -S-, -CO-, and a group combining them.
Examples of the substituent include halogen atoms such as fluorine atom, chlorine atom, bromine atom and iodine atom, alkoxy groups such as methoxy group, ethoxy group and propoxy group, alkoxycarbonyl groups such as methoxycarbonyl group and ethoxycarbonyl group, alkoxycarbonyloxy groups such as methoxycarbonyloxy group and ethoxycarbonyloxy group, and cyano group, nitro group and hydroxyl group, among the above-mentioned group "-A-C (=O) -N (R) 2" and the group "- (CR' 2)2 -OH)".
R 'in the group "- (CR' 2)2 -OH") is preferably a hydrogen atom from the viewpoint of improving the liquid crystal alignment.
The hydroxyalkylamide compound (B) represented by the above formula (1) is preferably a compound represented by the following formula (B-1). N in the following formula (b-1) is each independently, more preferably 2 to 10, still more preferably 2 to 8. More preferably, the compounds represented by the following formulas (Add-1) to (Add-2). The compounds represented by the following formulas (Add-1) to (Add-2) are novel compounds not disclosed in the prior art documents.
(In the formula (b-1), two n are each independently defined as above).
The preferable content of the hydroxyalkylamide compound (B) represented by the above formula (1) in the liquid crystal aligning agent of the present invention is preferably 0.1 to 50 parts by mass, more preferably 0.1 to 30 parts by mass, per 100 parts by mass of the component (a).
Process for producing polyamic acid
The polyamic acid as a polyimide precursor used in the present invention can be produced by the following method. Specifically, the tetracarboxylic acid component and the diamine component can be synthesized by a reaction (polycondensation reaction) in the presence of an organic solvent at, for example, from-20 to 150℃and preferably from 0 to 50℃for, for example, from 30 minutes to 24 hours and preferably from 1 to 12 hours.
Specific examples of the organic solvent used in the above reaction include: n-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, gamma-butyrolactone, N-dimethylformamide, N-dimethylacetamide, dimethylsulfoxide, 1, 3-dimethyl-2-imidazolidinone. In addition, in the polymer solvent solubility is high, can use methyl ethyl ketone, cyclohexanone, cyclopentanone, 4-hydroxy-4-methyl-2-pentanone or the following formula [ D-1] ~ formula [ D-3] solvent. They may be used in combination of two or more.
(In the formula [ D-1], D 1 represents an alkyl group having 1 to 3 carbon atoms, in the formula [ D-2], D 2 represents an alkyl group having 1 to 3 carbon atoms, in the formula [ D-3], D 3 represents an alkyl group having 1 to 4 carbon atoms).
The reaction may be carried out at any concentration, and is preferably 1 to 50% by mass, more preferably 5 to 30% by mass. The reaction may be carried out at a high concentration at the beginning of the reaction, and then a solvent may be added. In the reaction, the ratio of the total mole number of the diamine component to the total mole number of the tetracarboxylic acid component is preferably 0.8 to 1.2. As in the case of the usual polycondensation reaction, the molecular weight of the polyamide acid to be produced increases as the molar ratio approaches 1.0.
The polyamic acid obtained in the above reaction can be recovered by pouring the reaction solution into a poor solvent while stirring the solution sufficiently to precipitate the polyamic acid. Further, the powder of the purified polyamic acid can be obtained by performing precipitation several times, washing with a poor solvent, and drying at room temperature or by heating. The poor solvent is not particularly limited, and examples thereof include: water, methanol, ethanol, hexane, butyl cellosolve, acetone, toluene, etc.
In the case where the polyimide precursor is a polyamic acid ester, it can be produced by the following known method: (1) A method for esterifying a polyamic acid obtained from a tetracarboxylic dianhydride and a diamine; (2) A process based on the reaction of a tetracarboxylic diester dichloride with a diamine; (3) And a method of polycondensing a tetracarboxylic acid diester with a diamine.
The polyimide precursor may be a polymer having a modified terminal end, which is obtained by using an appropriate capping agent together with the tetracarboxylic acid derivative and diamine described above in the production of the polyimide precursor.
Examples of the terminal modifier include: anhydrides such as acetic anhydride, maleic anhydride, nadic anhydride, phthalic anhydride, itaconic anhydride, cyclohexanedicarboxylic anhydride, 3-hydroxyphthalic anhydride, trimellitic anhydride, and di-t-butyl dicarbonate; monoamine compounds such as aniline, 2-aminophenol, 3-aminophenol, 4-aminosalicylic acid, 5-aminosalicylic acid, 6-aminosalicylic acid, 2-aminobenzoic acid, 3-aminobenzoic acid, and 4-aminobenzoic acid; monoisocyanate compounds such as ethyl isocyanate, phenyl isocyanate and naphthyl isocyanate.
The proportion of the terminal modifier used is preferably 40 parts by mole or less, more preferably 30 parts by mole or less, based on 100 parts by mole of the total diamine component used.
Method for producing polyimide
The polyimide used in the present invention can be produced by: the polyamic acid or polyamic acid ester as a polyimide precursor is imidized by a known method.
For example, in the case of producing polyimide from polyamic acid, it is convenient to add a catalyst for (chemical) imidization to a solution of polyamic acid obtained by the reaction of a diamine component and a tetracarboxylic acid component. Imidization can be performed, for example, by stirring a polymer to be imidized in an organic solvent in the presence of a basic catalyst and an acid anhydride.
In polyimide, the ring closure rate (also referred to as imidization rate) of the functional group of the polyamic acid or polyamic acid ester is not necessarily 100%, and may be arbitrarily adjusted according to the application and purpose.
The polyimide obtained by imidizing the polyamic acid or polyamic acid ester may be obtained by: thermal imidization in which the solution of the polyamic acid or the polyamic acid ester is directly heated, or catalytic imidization in which a catalyst is added to the solution of the polyamic acid or the polyamic acid ester. The temperature at the time of thermal imidization is 100 to 400 ℃, preferably 120 to 250 ℃, and it is preferable to conduct the imidization while removing water generated by the imidization reaction from the system.
Catalytic imidization may be performed as follows: the basic catalyst and the acid anhydride are added to the polymer solution, and stirring is preferably performed at-20 to 250 ℃, more preferably at 0 to 180 ℃. The amount of the basic catalyst is preferably 0.5 to 30 mol times, more preferably 2 to 20 mol times, of the amide acid group or the amic acid ester group, and the amount of the acid anhydride is preferably 1 to 50 mol times, more preferably 3 to 30 mol times, of the amide acid group or the amic acid ester group. The basic catalyst may be: pyridine, triethylamine, trimethylamine, tributylamine, trioctylamine and the like are preferable, among them, pyridine has a moderate basicity for allowing the reaction to proceed. The acid anhydride includes: among them, acetic anhydride, trimellitic anhydride, pyromellitic anhydride, and the like are preferable because purification after completion of the reaction becomes easy if acetic anhydride is used. The imidization rate obtained by catalytic imidization can be controlled by adjusting the amount of the catalyst, the reaction temperature and the reaction time.
In the case of recovering the polyimide produced from the reaction solution that catalyzes imidization, the reaction solution may be poured into a solvent to precipitate the polyimide. As the solvent used for precipitation, there may be mentioned: methanol, ethanol, isopropanol, acetone, hexane, butyl cellosolve, heptane, methyl ethyl ketone, methyl isobutyl ketone, toluene, benzene, water, etc. The polymer precipitated by being added to the solvent may be dried by filtration and recovery at normal or reduced pressure, at normal temperature or by heating. Further, if the operation of re-precipitating and recovering the polymer obtained by precipitation and recovering is repeated 2 to 10 times to re-dissolve the polymer in the solvent, the impurities in the polymer can be reduced. Examples of the solvent include alcohols, ketones, and hydrocarbons, and if three or more solvents selected from these solvents are used, the purification efficiency is further improved, which is preferable.
Solution viscosity/molecular weight of Polymer
The polyamic acid, polyamic acid ester, and polyimide used in the present invention are preferably those having a solution viscosity of, for example, 10 to 1000mpa·s when they are prepared into a solution having a concentration of 10 to 15% by weight, from the viewpoint of workability, but are not particularly limited. The solution viscosity (mpa·s) of the polymer is a value measured at 25 ℃ using an E-type rotational viscometer, which is a polymer solution having a concentration of 10 to 15 mass% prepared using a good solvent (for example, γ -butyrolactone, N-methyl-2-pyrrolidone, etc.) for the polymer.
The weight average molecular weight (Mw) of the polyamic acid, polyamic acid ester, and polyimide in terms of polystyrene as measured by Gel Permeation Chromatography (GPC) is preferably 1000 to 500000, more preferably 2000 to 500000. The molecular weight distribution (Mw/Mn) shown by the ratio of Mw to the polystyrene-equivalent number average molecular weight (Mn) measured by GPC is preferably 15 or less, more preferably 10 or less. By setting the molecular weight to such a range, good liquid crystal alignment properties of the liquid crystal display element can be ensured.
< Liquid Crystal alignment agent >)
The liquid crystal aligning agent of the present invention comprises the polymer (A) having the ability to align liquid crystals and the hydroxyalkylamide compound (B) of the formula (1). The liquid crystal aligning agent of the present invention preferably has the following constitution: the hydroxyalkylamide compound (B) of the above formula (1) is added to a solution in which the polymer (A) having an ability to orient a liquid crystal is dissolved in a solvent.
The content (concentration) of the polymer (a) contained in the liquid crystal aligning agent of the present invention may be appropriately changed depending on the setting of the thickness of the coating film to be formed, and is preferably 1 mass% or more in terms of forming a uniform and defect-free coating film, and is preferably 10 mass% or less in terms of storage stability of the solution.
The solvent contained in the liquid crystal aligning agent is not particularly limited as long as the polymer component is uniformly dissolved. Specific examples thereof include: n, N-dimethylformamide, N-dimethylacetamide, N-dimethylformamide, N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, dimethylsulfoxide, gamma-butyrolactone, gamma-valerolactone, 1, 3-dimethyl-2-imidazolidinone, methylethylketone, cyclohexanone, cyclopentanone, 3-methoxy-N, N-dimethylpropionamide, 3-butoxy-N, N-dimethylpropionamide, N- (N-propyl) -2-pyrrolidone, N-isopropyl-2-pyrrolidone, N- (N-butyl) -2-pyrrolidone, N- (t-butyl) -2-pyrrolidone, N- (N-pentyl) -2-pyrrolidone, N-methoxypropyl-2-pyrrolidone, N-ethoxyethyl-2-pyrrolidone, N-methoxybutyl-2-pyrrolidone, N-cyclohexyl-2-pyrrolidone (which will also be collectively referred to as "good solvents"), and the like. Among them, N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, 3-methoxy-N, N-dimethylpropionamide, 3-butoxy-N, N-dimethylpropionamide or gamma-butyrolactone is preferable. The content of the good solvent is preferably 20 to 99% by mass, more preferably 20 to 90% by mass, and particularly preferably 30 to 80% by mass of the entire solvent contained in the liquid crystal aligning agent.
In addition, a mixed solvent of the solvent contained in the liquid crystal aligning agent and a solvent (also referred to as a poor solvent) that improves the coatability and the surface smoothness of the coating film when the liquid crystal aligning agent is coated is preferably used in addition to the above-mentioned solvent. Specific examples of the solvent to be used in combination are not limited thereto.
For example, there may be mentioned: diisopropyl ether, diisobutyl methanol (2, 6-dimethyl-4-heptanol), ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol dibutyl ether, 1, 2-butoxyethane, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, 4-hydroxy-4-methyl-2-pentanone, diethylene glycol methylethyl ether, diethylene glycol dibutyl ether, 3-ethoxybutyl acetate, 1-methylpentyl acetate, 2-ethylbutyl acetate, 2-ethylhexyl acetate, ethylene glycol monoacetate, ethylene glycol diacetate, propylene carbonate, ethylene glycol monobutyl ether, ethylene glycol monoisopentyl ether, ethylene glycol monohexyl ether, propylene glycol monobutyl ether, 1- (2-butoxyethoxy) -2-propanol 2- (2-butoxyethoxy) -1-propanol, propylene glycol monomethyl ether acetate, propylene glycol diacetate, dipropylene glycol monomethyl ether, dipropylene glycol monoethyl ether, dipropylene glycol dimethyl ether, ethylene glycol monobutyl ether acetate, diethylene glycol monoethyl ether acetate, diethylene glycol monobutyl ether acetate, 2- (2-ethoxyethoxy) ethyl acetate, diethylene glycol acetate, propylene glycol diacetate, n-butyl acetate, propylene glycol monoethyl ether acetate, methyl 3-methoxypropionate, ethyl 3-ethoxypropionate, ethyl 3-methoxypropionate, propyl 3-methoxypropionate, butyl 3-methoxypropionate, n-butyl lactate, isoamyl lactate, diethylene glycol monoethyl ether, diisobutylketone (2, 6-dimethyl-4-heptanone), and the like.
Among them, diisobutyl methanol, propylene glycol monobutyl ether, propylene glycol diacetate, diethylene glycol diethyl ether, dipropylene glycol monomethyl ether, dipropylene glycol dimethyl ether, 4-hydroxy-4-methyl-2-pentanone, ethylene glycol monobutyl ether acetate or diisobutyl ketone are preferable. The content of the poor solvent is preferably 1 to 80% by mass, more preferably 10 to 80% by mass, and particularly preferably 20 to 70% by mass of the entire solvent contained in the liquid crystal aligning agent. The type and content of the poor solvent are appropriately selected according to the application apparatus, application conditions, application environment, and the like of the liquid crystal aligning agent.
The preferable combination of the good solvent and the poor solvent includes: n-methyl-2-pyrrolidone and ethylene glycol monobutyl ether, N-methyl-2-pyrrolidone and gamma-butyrolactone and ethylene glycol monobutyl ether, N-ethyl-2-pyrrolidone and propylene glycol monobutyl ether, N-ethyl-2-pyrrolidone and 4-hydroxy-4-methyl-2-pentanone, N-ethyl-2-pyrrolidone and propylene glycol diacetate, N-dimethyl lactamide and diisobutyl ketone, N-methyl-2-pyrrolidone and 3-ethoxypropionic acid ethyl ester, N-ethyl-2-pyrrolidone and 3-ethoxypropionic acid ethyl ester, N-methyl-2-pyrrolidone and ethylene glycol monobutyl ether acetate, N-ethyl-2-pyrrolidone and dipropylene glycol dimethyl ether, N, N-dimethyl-lactonamide and ethylene glycol monobutyl ether, N-dimethyl-lactonamide and propylene glycol diacetate, N-ethyl-2-pyrrolidone and diethylene glycol diethyl ether, N-dimethyl-lactonamide and diethylene glycol diethyl ether, N-methyl-2-pyrrolidone and gamma-butyrolactone and 4-hydroxy-4-methyl-2-pentanone and diethylene glycol diethyl ether, N-ethyl-2-pyrrolidone and N-methyl-2-pyrrolidone and 4-hydroxy-4-methyl-2-pentanone, N-ethyl-2-pyrrolidone and 4-hydroxy-4-methyl-2-pentanone and propylene glycol monobutyl ether, N-methyl-2-pyrrolidone and 4-hydroxy-4-methyl-2-pentanone and 2, 6-dimethyl-4-heptanone, N-methyl-2-pyrrolidone and 4-hydroxy-methyl-2-pentanone and dipropylene glycol monomethyl ether, N-methyl-2-pyrrolidone and 4-hydroxy-4-methyl-2-pentanone and propylene glycol monobutyl ether, N-methyl-2-pyrrolidone and 4-hydroxy-4-methyl-2-pentanone and propylene glycol diacetate, gamma-butyrolactone and 4-hydroxy-4-methyl-2-pentanone and 2, 6-dimethyl-4-heptanone, gamma-butyrolactone and 4-hydroxy-4-methyl-2-pentanone and propylene glycol diacetate, N-methyl-2-pyrrolidone and gamma-butyrolactone and propylene glycol monobutyl ether and 2, 6-dimethyl-4-heptanone, N-methyl-2-pyrrolidone and gamma-butyrolactone and propylene glycol monobutyl ether and diisopropyl ether, N-methyl-2-pyrrolidone and gamma-butyrolactone and propylene glycol monobutyl ether and 2, 6-dimethyl-4-heptanol, N-methyl-2-pyrrolidone and gamma-butyrolactone and dipropylene glycol dimethyl ether; n-methyl-2-pyrrolidone and propylene glycol monobutyl ether and dipropylene glycol dimethyl ether; n-ethyl-2-pyrrolidone and propylene glycol monobutyl ether and dipropylene glycol monomethyl ether; n-ethyl-2-pyrrolidone with propylene glycol monobutyl ether and propylene glycol diacetate; n-ethyl-2-pyrrolidone and propylene glycol monobutyl ether and diisobutyl ketone; n-ethyl-2-pyrrolidone and gamma-butyrolactone and diisobutyl ketone; n-ethyl-2-pyrrolidone, N-dimethyl lactamide, diisobutyl ketone, and the like.
The liquid crystal aligning agent of the present invention may further contain a component other than a solvent (hereinafter, also referred to as an additive component) in addition to the polymer (a) and the hydroxyalkylamide compound (B). Examples of such additive components include: an adhesion promoter for improving adhesion between the liquid crystal alignment film and the substrate and adhesion between the liquid crystal alignment film and the sealing material; a compound for improving the strength of the liquid crystal alignment film (hereinafter, also referred to as a crosslinkable compound); dielectric materials, conductive materials, and the like for adjusting the dielectric constant and resistance of the liquid crystal alignment film.
The crosslinkable compound may be a compound selected from the group consisting of: a compound having at least one group selected from the group consisting of an oxirane group, an oxetane group, a protected isocyanate group, a protected isothiocyanate group, a group containing an oxazoline ring structure, a group containing a Mi acid structure, and a cyclic carbonate group; a hydroxyalkylamide compound other than the compound represented by the above formula (1) or a compound represented by the following formula (e).
In the formula (e), A represents an (m+n) -valent organic group having an aromatic ring, m represents an integer of 1 to 6, n represents an integer of 0 to 4, R represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, and any hydrogen atom of the aromatic ring is optionally substituted with a halogen atom, an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a fluoroalkyl group having 1 to 10 carbon atoms, a fluoroalkenyl group having 2 to 10 carbon atoms, or a fluoroalkoxy group having 1 to 10 carbon atoms, and R is each independently defined above when m is 2 or more.
Specific examples of the compound having an oxirane group include: compounds having two or more oxirane groups, such as the compound described in paragraph [0037] of JP-A-10-338880 and the compound having a triazine ring in the skeleton described in International publication No. 2017/170483, are used. Among them, compounds containing nitrogen atoms such as N, N, N ', N ' -tetraglycidyl m-xylylenediamine, 1, 3-bis (N, N-diglycidyl aminomethyl) cyclohexane, N, N, N ', N ' -tetraglycidyl-4, 4' -diaminodiphenylmethane, N, N, N ', N ' -tetraglycidyl-p-phenylenediamine, and compounds represented by the following formulas (r-1) to (r-3) may be used.
Specific examples of the compounds having an oxetanyl group include compounds having two or more oxetanyl groups described in paragraphs [0170] to [0175] of International publication No. 2011/132751.
Specific examples of the compound having a protected isocyanate group include: the compounds having two or more protected isocyanate groups described in paragraphs [0046] to [0047] of Japanese patent application laid-open No. 2014-224978, the compounds having three or more protected isocyanate groups described in paragraphs [0119] to [0120] of International publication No. 2015/141598, and the like may be those represented by the following formulas (bi-1) to (bi-3).
Specific examples of the compound having a protected isothiocyanate group include compounds having two or more protected isothiocyanate groups described in Japanese patent application laid-open No. 2016-200798.
Specific examples of the compound having a group containing an oxazoline ring structure include compounds containing two or more oxazoline structures described in paragraph [0115] of JP-A2007-286597.
Specific examples of the compound having a group containing a Mi's acid structure include compounds having two or more Mi's acid structures described in International publication No. 2012/091088.
Specific examples of the compound having a cyclic carbonate group include compounds described in international publication No. 2011/155577.
Specific examples of the hydroxyalkylamide compound other than the compound represented by the above formula (1) include: the compounds described in International publication No. 2015/072554, paragraph [0058] of Japanese patent application laid-open No. 2016-118753, the compounds described in Japanese patent application laid-open No. 2016-200798, the compounds described in International publication No. 2019/142927, and the like may be those represented by the following formulas (hd-1) to (hd-8), or those represented by the following formulas (hd 1-1) to (hd 1-4).
Examples of the (m+n) -valent organic group having an aromatic ring in a of the above formula (e) include: an (m+n) -valent aromatic hydrocarbon group having 6 to 30 carbon atoms, an (m+n) -valent organic group obtained by bonding an aromatic hydrocarbon group having 6 to 30 carbon atoms directly or via a linking group, and an (m+n) -valent group having an aromatic heterocycle. Examples of the aromatic hydrocarbon include benzene and naphthalene. Examples of the aromatic heterocycle include: pyrrole ring, imidazole ring, pyrazole ring, pyridine ring, pyrimidine ring, quinoline ring, isoquinoline ring, carbazole ring, pyridazine ring, pyrazine ring, benzimidazole ring, indole ring, quinoxaline ring, acridine ring, and the like. Examples of the linking group include: an alkylene group having 1 to 10 carbon atoms, a group obtained by removing one hydrogen atom from the alkylene group, a divalent or trivalent cyclohexane ring, or the like. Any hydrogen atom of the alkylene group is optionally substituted with an organic group such as an alkyl group having 1 to 6 carbon atoms, a fluorine atom or a trifluoromethyl group. Specific examples thereof include compounds described in International publication No. 2010/074269 and compounds represented by the following formulas (e-1) to (e-10).
The above-mentioned compound is an example of a crosslinkable compound, but is not limited thereto. Examples of the composition include those other than those disclosed in pages [0105] to [0116] of pages 53 and [0105] to [ 55 ] of International publication No. 2015/060357. Further, two or more kinds of crosslinkable compounds may be combined.
The content of the crosslinkable compound in the liquid crystal aligning agent of the present invention is preferably 0.5 to 20 parts by mass, more preferably 1 to 15 parts by mass, in terms of proceeding the crosslinking reaction and exhibiting good resistance to AC residual images, relative to 100 parts by mass of the polymer component contained in the liquid crystal aligning agent.
Examples of the adhesion promoter include: 3-aminopropyl trimethoxysilane, 3-aminopropyl triethoxysilane, 3-aminopropyl diethoxymethyl silane, 2-aminopropyl trimethoxysilane, 2-aminopropyl triethoxysilane, N- (2-aminoethyl) -3-aminopropyl trimethoxysilane, N- (2-aminoethyl) -3-aminopropyl methyldimethoxysilane, 3-ureidopropyl trimethoxysilane, 3-ureidopropyl triethoxysilane, N-ethoxycarbonyl-3-aminopropyl trimethoxysilane, N-ethoxycarbonyl-3-aminopropyl triethoxysilane, N-triethoxysilylpropyl triethylenetriamine, N-trimethoxysilylpropyl triethylenetriamine, 10-trimethoxysilyl-1, 4, 7-triazadecane 10-triethoxysilyl-1, 4, 7-triazadecane, 9-trimethoxysilyl-3, 6-diazanonylacetate, 9-triethoxysilyl-3, 6-diazanonylacetate, N-benzyl-3-aminopropyl trimethoxysilane, N-benzyl-3-aminopropyl triethoxysilane, N-phenyl-3-aminopropyl trimethoxysilane, N-phenyl-3-aminopropyl triethoxysilane, N-bis (oxyethylene) -3-aminopropyl trimethoxysilane, N-bis (oxyethylene) -3-aminopropyl triethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, 2- (3, 4-epoxycyclohexyl) ethyltrimethoxysilane, 3-epoxypropoxy propylmethyldimethoxysilane, silane coupling agents such as 3-glycidoxypropyl trimethoxysilane, 3-glycidoxypropyl methyl diethoxysilane, 3-glycidoxypropyl triethoxysilane, p-styryl trimethoxysilane, 3-methacryloxypropyl methyl dimethoxysilane, 3-methacryloxypropyl trimethoxysilane, 3-methacryloxypropyl methyl diethoxysilane, 3-methacryloxypropyl triethoxysilane, 3-acryloxypropyl trimethoxysilane, tris- (trimethoxysilylpropyl) isocyanurate, 3-mercaptopropyl methyl dimethoxysilane, 3-mercaptopropyl trimethoxysilane, and 3-isocyanatopropyl triethoxysilane. When the silane coupling agent is used, it is preferably 0.1 to 30 parts by mass, more preferably 0.1 to 20 parts by mass, per 100 parts by mass of the polymer component contained in the liquid crystal aligning agent, from the viewpoint of exhibiting good resistance to AC residual shadows.
Liquid crystal alignment film/liquid crystal display element
The liquid crystal alignment film of the present invention is obtained from the liquid crystal alignment agent. The liquid crystal alignment film of the present invention can be used for a liquid crystal alignment film of a liquid crystal display element of a horizontal alignment type or a vertical alignment type (VA type), and among them, a liquid crystal alignment film suitable for a liquid crystal display element of a horizontal alignment type such as an IPS system or FFS system is preferable. The liquid crystal display element of the present invention includes the liquid crystal alignment film. The liquid crystal display element of the present invention can be manufactured by a method including the following steps (1) to (4) or steps (1) to (2) and (4), for example.
< Procedure (1): process for coating liquid Crystal alignment agent
The liquid crystal aligning agent of the present invention is applied to one surface of a substrate provided with a patterned transparent conductive film by a suitable application method such as roll coater method, spin coating method, printing method, ink jet method, or the like. The substrate is not particularly limited as long as it is a substrate having high transparency, and a plastic substrate such as an acrylic substrate or a polycarbonate substrate may be used together with a glass substrate or a silicon nitride substrate. In the reflective liquid crystal display element, if the substrate is a single-sided substrate, an opaque material such as a silicon wafer may be used, and in this case, a material reflecting light such as aluminum may be used as the electrode. In the case of manufacturing an IPS type or FFS type liquid crystal device, a substrate provided with an electrode formed of a transparent conductive film or a metal film patterned into a comb-teeth type and a counter substrate not provided with an electrode are used.
Examples of the method of applying the liquid crystal aligning agent to the substrate and forming a film include: screen printing, offset printing, flexography, inkjet or spray printing, and the like. Among them, a method of coating and film formation by an inkjet method can be preferably used.
< Procedure (2): firing the applied liquid crystal aligning agent
The step (2) is a step of firing the liquid crystal aligning agent applied to the substrate to form a film. After the liquid crystal alignment agent is coated on the substrate, the solvent may be evaporated by a heating unit such as a hot plate, a thermal circulation type oven or an IR (infrared) type oven, or the thermal imidization of the amic acid or amic acid ester in the polymer may be performed. The drying and firing steps after the application of the liquid crystal aligning agent of the present invention may be performed at any temperature and for any time or may be performed a plurality of times. The temperature of the solvent for removing the liquid crystal aligning agent may be, for example, 40 to 180 ℃. From the viewpoint of shortening the process, it may be carried out at 40 to 150 ℃. The firing time is not particularly limited, and may be 1 to 10 minutes or 1 to 5 minutes. In the case of thermal imidization of the amic acid or amic acid ester in the polymer, the step of removing the organic solvent may be followed by a step of firing at a temperature ranging from 150 to 300 ℃ or from 150 to 250 ℃. The firing time is not particularly limited, and firing time of 5 to 40 minutes or 5 to 30 minutes may be mentioned.
If the thickness of the film after firing is too small, the reliability of the liquid crystal display element may be lowered, and therefore the thickness is preferably 5 to 300nm, more preferably 10 to 200nm.
< Procedure (3): a step of orienting the film obtained in the step (2)
The step (3) is a step of optionally subjecting the film obtained in the step (2) to an orientation treatment. That is, in a liquid crystal display element of a horizontal alignment type such as an IPS type or FFS type, the coating film is subjected to an alignment ability imparting treatment. On the other hand, in a vertical alignment type liquid crystal display element such as VA mode or PSA mode, the formed coating film may be used as a liquid crystal alignment film as it is, or the coating film may be subjected to an alignment ability imparting treatment. The alignment treatment method of the liquid crystal alignment film is preferably a rubbing treatment method or a photo-alignment treatment method. As the photo-alignment treatment method, the following method can be mentioned: the film is irradiated with radiation biased in a fixed direction on the surface thereof, and if necessary, it is preferable to heat the film at a temperature of 150 to 250 ℃ to impart liquid crystal alignment (also referred to as liquid crystal alignment ability). As the radiation, ultraviolet or visible light having a wavelength of 100 to 800nm can be used. Among them, ultraviolet rays having a wavelength of 100 to 400nm are preferable, and ultraviolet rays having a wavelength of 200 to 400nm are more preferable.
The irradiation amount of the above-mentioned radioactive rays is preferably 1 to 10000mJ/cm 2. Among them, 100 to 5000mJ/cm 2 is preferable. In the case of irradiation with radiation, the substrate having the film may be irradiated with radiation while being heated at 50 to 250 ℃ in order to improve the alignment of the liquid crystal. The liquid crystal alignment film produced as described above can stably align liquid crystal molecules in a fixed direction.
In the above method, the liquid crystal alignment film irradiated with the polarized radiation may be subjected to a contact treatment with water or a solvent, or the liquid crystal alignment film irradiated with the radiation may be subjected to a heat treatment.
The solvent used in the contact treatment is not particularly limited as long as it is a solvent that dissolves a decomposition product formed from the film-like material upon irradiation with radiation. As specific examples, there may be mentioned: water, methanol, ethanol, 2-propanol, acetone, methyl ethyl ketone, 1-methoxy-2-propanol acetate, butyl cellosolve, ethyl lactate, methyl lactate, diacetone alcohol, methyl 3-methoxypropionate, ethyl 3-ethoxypropionate, propyl acetate, butyl acetate, cyclohexyl acetate, and the like. Among them, water, 2-propanol, 1-methoxy-2-propanol or ethyl lactate is preferable in view of versatility and safety of solvents. More preferably water, 1-methoxy-2-propanol or ethyl lactate. The solvent may be one kind or two or more kinds may be combined.
The heat treatment of the above-mentioned coating film irradiated with radiation is preferably carried out at 50 to 300℃for 1 to 30 minutes, more preferably at 120 to 250℃for 1 to 30 minutes.
< Procedure (4): process for manufacturing liquid Crystal cell
Two substrates on which the liquid crystal alignment film was formed as described above were prepared, and liquid crystal was disposed between the two substrates disposed opposite to each other. Specifically, the following two methods are exemplified. In the first method, first, two substrates are arranged to face each other with a gap (cell gap) therebetween so that the liquid crystal alignment films face each other. Next, the peripheral portions of the two substrates are bonded together with a sealant, and a liquid crystal composition is injected into a cell gap defined by the substrate surface and the sealant, and the liquid crystal composition is brought into contact with the film surface, and then the injection hole is sealed.
The second method is a method called an ODF (One Drop Fill) method. A liquid crystal composition is dispensed onto a predetermined portion of one of the two substrates on which the liquid crystal alignment film is formed, for example, by applying an ultraviolet curable sealant to a predetermined portion of the liquid crystal alignment film surface. Then, the liquid crystal composition is bonded to the other substrate so as to face the liquid crystal alignment film, and pushed to the entire surface of the substrate to be in contact with the film surface. Then, the entire surface of the substrate is irradiated with ultraviolet light to cure the sealant. In either method, it is desirable to further heat the liquid crystal composition to be used to a temperature at which the liquid crystal composition is in phase in each direction, and then slowly cool the liquid crystal composition to room temperature, thereby removing the flow alignment at the time of filling the liquid crystal.
When the coating film is subjected to the rubbing treatment, the two substrates are disposed so that the rubbing directions of the respective coating films are at a predetermined angle, for example, orthogonal or antiparallel to each other.
As the sealant, for example, an epoxy resin containing a curing agent and alumina balls as spacers, or the like can be used. The liquid crystal includes nematic liquid crystal and smectic liquid crystal, and among them, nematic liquid crystal is preferable.
Then, a polarizing plate is attached to the outer surface of the liquid crystal cell as needed, whereby a liquid crystal display element can be obtained. Examples of the polarizing plate attached to the outer surface of the liquid crystal cell include a polarizing plate in which a polarizing film called "H film" in which iodine is absorbed while stretching and orienting polyvinyl alcohol is sandwiched between cellulose acetate protective films, and a polarizing plate composed of the H film itself.
The liquid crystal display element of the present invention can be effectively applied to various devices, for example, various display devices such as a clock, a portable game machine, a word processor, a notebook personal computer, a car navigation system, a video camera (camcorder), a PDA, a digital camera, a cellular phone, a smart phone, various monitors, a liquid crystal television, and an information display. The polymer composition contained in the liquid crystal aligning agent may be used for a liquid crystal alignment film for a retardation film, a scanning antenna, a liquid crystal alignment film for a liquid crystal array antenna, a liquid crystal alignment film for a liquid crystal light adjusting element for a transmission scattering type, or for other applications, for example, a protective film for a color filter, a gate insulating film for a flexible display, and a substrate material.
Examples
The present invention will be described in more detail with reference to examples, but the present invention is not limited thereto. The abbreviations of the compounds and the measurement methods of the respective characteristics are shown below. In addition, "TMS" represents trimethylsilyl.
(Tetracarboxylic dianhydride)
CA-1: a compound represented by the following formula (CA-1).
(Diamine)
DA-1: a compound represented by the following formula (DA-1).
(Hydroxyalkylamide Compound)
Add-1, add-2: compounds represented by the following formulas (Add-1) and (Add-2), respectively.
(Additive)
Add-C1, add-C2: compounds represented by the following formulas (Add-C1) and (Add-C2), respectively.
Add-S1: a compound represented by the following formula (Add-S1).
(Organic solvent)
NMP: n-methyl-2-pyrrolidone.
BCS: ethylene glycol monobutyl ether.
DMF: n, N-dimethylformamide.
< 1 Determination by H-NMR >
The device comprises: a Fourier transform type superconducting nuclear magnetic resonance apparatus (FT-NMR) 'AVANCE III' (manufactured by BRUKER) was 500MHz.
Solvent: deuterated dimethyl sulfoxide ([ D 6 ] -DMSO). Standard substance: tetramethylsilane.
< Determination of viscosity >
The viscosity of the solution was measured at 25℃using an E-viscometer TVE-22H (manufactured by eastern machine Co., ltd.) and a sample size of 1.1mL using a conical rotor TE-1 (1℃34', R24).
< Determination of molecular weight >
The molecular weight was measured by a normal temperature GPC (gel permeation chromatography) apparatus, and the number average molecular weight (Mn) and the weight average molecular weight (Mw) were calculated as polyethylene glycol and polyethylene oxide converted values.
GPC apparatus: GPC-101 (manufactured by Showa electric company), column: GPC KD-803, GPC KD-805 (manufactured by Showa electric company) series connection, column temperature: 50 ℃, eluent: n, N-dimethylformamide (as additive, lithium bromide monohydrate (LiBr. H2O) was 30mmol/L, phosphoric acid-anhydrous crystal (O-phosphoric acid) was 30mmol/L, tetrahydrofuran (THF) was 10 mL/L), flow rate: 1.0 mL/min.
Standard sample for calibration curve preparation: TSK standard polyethylene oxides (molecular weight; about 900000, 150000, 100000 and 30000) (manufactured by TOSOH Co.) and polyethylene glycols (molecular weight; about 12000, 4000 and 1000) (manufactured by Polymer Laboratories Co.).
Synthesis of hydroxyalkylamide Compound
Synthesis example 1 (Add-1) >)
Compound (Add-1) was synthesized according to the route shown below.
(Synthesis of first step Compound (1 a))
To 4,4' -biphenol (9.30 g,50.0 mmol) was added ethyl 4-chlorobutyrate (18.1 g,120mmol,2.4 eq.), potassium carbonate (20.7 g,150 mmol), potassium iodide (0.830 g,5 mmol) and DMF (93.0 g), and the mixture was heated at 100℃for 20 hours. After completion of the reaction, water (344 g) was added to the filtrate obtained by filtering potassium carbonate to precipitate crystals, and the compound (1 a) was removed by filtration. The compound (1 a) was used as it is in the next step.
(Synthesis of Compound (2 a) in the second step)
To a mixed solution of a solution of potassium hydroxide (16.8 g,300 mmol) dissolved in water (117 g) and ethanol (46.5 g), the compound (1 a) obtained above was added in the entire amount, and the mixture was stirred at 80℃for 20 hours to carry out hydrolysis reaction. After completion of the reaction, 2N hydrochloric acid (200 mL,400 mmol) was added to neutralize the reaction, and crystals were precipitated. After recovery by filtration, cake washing was performed four times with water (195 g), and cake washing was performed with hexane (195 g), followed by drying under reduced pressure, whereby compound (2 a) (15.8 g,44.1mmol, two-stage yield: 88.2%) was obtained.
(Synthesis of third step Compound (3 a))
To compound (2 a) (3.20 g,8.92 mmol) were added toluene (28.8 g), DMF (10.0 mg) and oxalyl chloride (3.39 g,26.7 mmol), and the mixture was stirred at 60℃for 4 hours. After the completion of the reaction, the reaction solution was concentrated to obtain compound (3 a). The compound (3 a) was used as it is in the next step.
(Synthesis of fourth Process Compound (4 a))
The entire amount of the compound (3 a) obtained above was dissolved in methylene chloride (93.3 g), transferred to a 300mL four-necked flask, and a mixture of triethylamine (3.61 g,35.7 mmol) and a trimethylsilyl protector of diethanolamine (4.45 g,17.8 mmol) was added dropwise under ice bath over 15 minutes to effect amidation. The trimethylsilyl protector of diethanolamine was synthesized by reference to the method described in WO 2009/046536. After the completion of the dropwise addition, the mixture was stirred for 1 hour, and then water (32.4 g) was added thereto for washing by liquid separation. The organic layer was washed again with water (32.4 g) and the obtained organic layer was dehydrated with anhydrous magnesium sulfate (10 g) and dried under reduced pressure, whereby an oily compound (4 a) (6.68 g,8.13mmol, two-stage yield: 91.1%) was obtained.
(Fifth step Add-1 Synthesis)
Acetonitrile (66.8 g), acetic acid (3.34 g) and methanol (33.0 g) were added to the above-obtained compound (4 a) (6.68 g,8.13 mmol), and the mixture was heated at 40℃for 48 hours. After completion of the reaction, the solvent was distilled off and dried to give Add-1 (4.17 g,7.83mmol, yield: 96.2%).
From the result of 1 H-NMR shown below, it was confirmed that this compound was Add-1.
1H-NMR(500MHz,[D6]-DMSO):δ=7.52(d,4H,J=8.5Hz),6.99(d,4H,J=8.5Hz),4.70(br,4H),4.00(t,4H,J=6.4Hz),3.52-3.47(m,8H),3.40-3.35(m,8H),2.52(t,4H,J=7.2Hz),1.95(quin,4H,J=6.6Hz)
Synthesis example 2 (Add-2) >
Compound (Add-2) was synthesized according to the route shown below.
(Synthesis of first step Compound (1 b))
Compound (1 b) was obtained by the same method as the synthesis of compound (1 a) except that 9.27g (49.8 mmol) of 2,2 '-biphenol was used instead of 4,4' -biphenol.
(Synthesis of Compound (2 b) in the second step)
The synthesis was performed in the same manner as the synthesis of compound (2 a) except that compound (1 b) was used instead of compound (1 a), to obtain 16.8g (46.9 mmol, two-stage yield: 94.1%) of compound (2 b).
(Synthesis of third step Compound (3 b))
Compound (3 b) was obtained by the same method as for the synthesis of compound (3 a), except that 3.55g (9.90 mmol) of compound (2 b) was used instead of compound (2 a).
(Synthesis of fourth Process Compound (4 b))
Compound (4 b) was obtained in 7.60g (9.25 mmol, two-stage yield: 93.4%) by the same method as the synthesis of compound (4 a) except that compound (3 b) was used instead of compound (3 a).
(Fifth step Add-2 Synthesis)
Add-2 was obtained in 4.90g (9.20 mmol, yield: 99.5%) by the same method as the synthesis of (Add-1) except that compound (4 b) was used instead of compound (4 a).
From the result of 1 H-NMR shown below, it was confirmed that this compound was Add-2.
1H-NMR(500MHz,[D6]-DMSO):δ=7.29(t,2H,J=8.2Hz),7.16(d,2H,J=7.9Hz),7.05(d,2H,J=8.2Hz),6.97(t,2H,J=7.3Hz),4.70(br,4H),3.94(t,4H,J=6.5Hz),3.46-3.42(m,8H),3.32-3.27(m,8H),2.31(t,4H,J=8.0Hz),1.77(quin,4H,J=7.1Hz).
Preparation of liquid Crystal alignment agent
Example 1 >
DA-1 (14.3 g,50.0 mmol) and NMP (145 g) were added to a 100mL four-necked flask equipped with a stirrer and a nitrogen inlet tube, and the mixture was dissolved by stirring at room temperature under a nitrogen atmosphere. Then, CA-1 (10.5 g,48.0 mmol) and NMP (36.4 g) were added and stirred at 50℃for 16 hours to give a solution (viscosity: 525 mPas) of polyamic acid (PAA-1) having a concentration of 12%. The polyamide acid (PAA-1) had Mn of 14800 and Mw of 32500.
NMP (4.61 g), BCS (3.75 g), add-S1 (1% by mass NMP solution, 0.680 g) and Add-1 (10% by mass NMP solution, 0.340 g) were added to the above polyamic acid (PAA-1) solution (5.63 g), and stirred at room temperature for 3 hours, thereby obtaining a liquid crystal aligning agent (AL-1).
Example 2 >
NMP (4.28 g), BCS (3.75 g), add-S1 (1% by mass NMP solution, 0.680 g) and Add-1 (10% by mass NMP solution, 0.680 g) were added to the above polyamic acid (PAA-1) solution (5.63 g), and stirred at room temperature for 3 hours, thereby obtaining a liquid crystal aligning agent (AL-2).
Example 3 >
NMP (4.61 g), BCS (3.75 g), add-S1 (1% by mass NMP solution, 0.680 g) and Add-2 (10% by mass NMP solution, 0.340 g) were added to the above polyamic acid (PAA-1) solution (5.63 g), and stirred at room temperature for 3 hours, thereby obtaining a liquid crystal aligning agent (AL-3).
Example 4 >
NMP (4.28 g), BCS (3.75 g), add-S1 (1% by mass NMP solution, 0.680 g) and Add-2 (10% by mass NMP solution, 0.680 g) were added to the above polyamic acid (PAA-1) solution (5.63 g), and stirred at room temperature for 3 hours, thereby obtaining a liquid crystal aligning agent (AL-4).
Comparative example 1 >
NMP (4.61 g), BCS (3.75 g), add-S1 (1% by mass NMP solution, 0.680 g) and Add-C1 (10% by mass NMP solution, 0.340 g) were added to the above polyamic acid (PAA-1) solution (5.63 g), and stirred at room temperature for 3 hours, thereby obtaining a liquid crystal aligning agent (AL-5).
Comparative example 2 >
NMP (4.28 g), BCS (3.75 g), add-S1 (1% by mass NMP solution, 0.680 g) and Add-C1 (10% by mass NMP solution, 0.680 g) were added to the above polyamic acid (PAA-1) solution (5.63 g), and stirred at room temperature for 3 hours, thereby obtaining a liquid crystal aligning agent (AL-6).
Comparative example 3 >
NMP (4.95 g), BCS (3.75 g), add-S1 (1 mass% NMP solution, 0.680 g) and Add-C2 (0.0338 g) were added to the above polyamic acid (PAA-1) solution (5.63 g), and stirred at room temperature for 3 hours, thereby obtaining a liquid crystal aligning agent (AL-7).
Comparative example 4 >
NMP (4.95 g), BCS (3.75 g), add-S1 (1 mass% NMP solution, 0.680 g) and Add-C2 (0.0675 g) were added to the above polyamic acid (PAA-1) solution (5.63 g), and stirred at room temperature for 3 hours, thereby obtaining a liquid crystal aligning agent (AL-8).
Comparative example 5 >
NMP (4.95 g), BCS (3.75 g) and Add-S1 (1 mass% NMP solution, 0.680 g) were added to the solution (5.63 g) of the above polyamide acid (PAA-1), and stirred at room temperature for 3 hours, thereby obtaining a liquid crystal aligning agent (AL-9).
< Evaluation of Friction resistance >
First, a glass substrate with an ITO electrode on the entire surface was prepared. The substrate was a glass substrate having a thickness of 1.1mm and a size of 30mm×40mm, and an ITO electrode having a film thickness of 35nm was formed on the entire surface of the substrate. Next, the liquid crystal aligning agents AL-1 to AL-9 obtained in the examples and comparative examples were filtered by a filter having a pore diameter of 1.0 μm, and then applied to the ITO surface of the prepared electrode-equipped substrate by spin coating. After drying on a heating plate at 80℃for 2 minutes, baking was performed for 20 minutes using an infrared heating furnace at 230℃to form a coating film having a film thickness of 100nm, thereby obtaining a polyimide film. The polyimide film was subjected to a rubbing treatment (roll diameter: 120mm, roll rotation speed: 1000rpm, moving speed: 20mm/sec, pressing length: 0.4 mm) with a rayon cloth. The present substrate was observed with a microscope, and the film surface was evaluated by defining a case where streaks and chips due to the rubbing treatment were not observed at all as "excellent", a case where slag was slightly observed as "good", and a case where serious streaks and chips were observed as "×".
< Evaluation of anisotropy >)
The substrate subjected to the rubbing treatment was evaluated for anisotropy by using a liquid crystal alignment film evaluation system (LAYSCAN LYS-LH 30S-1A) (Moritex Co., ltd.) in the same manner as the above-described evaluation of the rubbing resistance. The case where the anisotropy was 0.15 or more was defined as "good", the case where it was 0.1 or more and less than 0.15 was defined as "good", and the case where it was less than 0.1 was defined as "x", and the evaluation was performed.
Production of liquid Crystal cell for evaluation of sealing adhesion
First, a glass substrate with an ITO electrode on the entire surface was prepared. The substrate was a glass substrate having a thickness of 1.1mm and a size of 30mm×40mm, and an ITO electrode having a film thickness of 35nm was formed on the entire surface of the substrate. Next, the liquid crystal aligning agents AL-1 to AL-9 obtained in the examples and comparative examples were filtered by a filter having a pore diameter of 1.0 μm, and then applied to the ITO surface of the prepared electrode-equipped substrate by spin coating. After drying on a heating plate at 80℃for 2 minutes, baking was performed for 20 minutes using an infrared heating furnace at 230℃to form a coating film having a film thickness of 100nm, thereby obtaining a polyimide film. The polyimide film was subjected to rubbing treatment (roller diameter: 120mm, roller rotation speed: 500rpm, moving speed: 30mm/sec, pressing length: 0.3mm, rubbing direction: direction inclined by 10 ° with respect to the IZO comb teeth electrode of the third layer), then subjected to ultrasonic irradiation in pure water for 1 minute to clean, and water droplets were removed by air blowing, and dried at 80℃for 10 minutes to obtain a substrate with a liquid crystal alignment film. Next, spacers of 4 μm are spread on the liquid crystal alignment film surface of one substrate, and a sealant (723K 1) (manufactured by co-chemical industry company) is applied to the liquid crystal alignment film surface of the other substrate, and the substrates are bonded so that the liquid crystal alignment film surfaces of the substrates face each other and so that the rubbing directions are opposite to each other. At this time, both substrate ends were overlapped by 1cm, and the application amount of the sealant was adjusted so that the diameter of the sealant after bonding became 3mm and reached the center portion of the region where the substrates were overlapped. Then, the bonded substrate was irradiated with ultraviolet rays having a wavelength of 365nm converted to 3J/cm 2 using a metal halide lamp having an illuminance of 20mW/cm 2, and then subjected to heat treatment at 120℃for 60 minutes using a thermal cycle type clean oven, to prepare a box for evaluating adhesion.
< Evaluation of seal adhesion >
The seal adhesion was evaluated by using a bench-type precision universal tester (AGS-X500N) (manufactured by shimadzu corporation). Specifically, after fixing the end portions of the upper and lower substrates of the obtained cassette, the overlapped portions of the two substrates were pressed from above at a speed of 5mm per second, and the pressure (N) at the time of peeling was measured. Then, the sealing adhesion was evaluated using a value obtained by normalizing the pressure (N) with the measured area (cm 2) estimated from the diameter of the sealant. The larger the value of the breaking strength, the more excellent the adhesion, i.e., the more excellent the present evaluation. The evaluation was performed by defining the case where the pressure was 1.5N/cm 2 or more as "good" and the case where the pressure was less than 1.5N/cm 2 as "X".
Production of liquid Crystal cell for evaluation of Voltage holding Rate
First, a substrate with electrodes is prepared. The substrate was a glass substrate having a size of 30mm by 40mm and a thickness of 0.7 mm. An ITO electrode having a film thickness of 35nm was formed on the substrate, and the electrode had a stripe pattern having a length of 40mm and a width of 10 mm.
Next, the liquid crystal aligning agents AL-1 to AL-9 obtained in the examples and comparative examples were filtered by a filter having a pore diameter of 1.0 μm, and then applied to the prepared electrode-equipped substrate by spin coating. After drying on a heating plate at 80℃for 2 minutes, baking was performed for 20 minutes in an infrared heating furnace at 230℃to form a coating film having a film thickness of 100nm, thereby obtaining a substrate with a polyimide film. After rubbing the polyimide film with a rayon cloth (roller diameter: 120mm, roller rotation speed: 1000rpm, moving speed: 20mm/sec, pressing length: 0.4 mm), the polyimide film was subjected to ultrasonic irradiation in pure water for 1 minute to clean the polyimide film, and water droplets were removed by air blowing and dried at 80℃for 10 minutes to obtain a substrate with a liquid crystal alignment film. Two substrates with the liquid crystal alignment film were prepared, and after a spacer of 4 μm was spread on the surface of one of the liquid crystal alignment films, a sealant was printed thereon, and the other substrate was bonded so that the rubbing direction was opposite and the film surfaces were opposed. Then, the sealant was cured to produce an empty box. The negative type liquid crystal MLC-7026-100 (manufactured by Merck) was injected into the empty cell by vacuum injection, and the injection port was sealed to obtain a liquid crystal cell. The resulting cell was then heated at 120℃for 1 hour and left at 23℃for one night for evaluation.
< Evaluation of Voltage maintenance Rate >)
The voltage of 1V was applied to the above-mentioned liquid crystal cell at 60℃for 60 μsec, and the voltage after 166.7msec was measured, and the voltage was calculated as the voltage holding ratio. The higher the value of the voltage holding ratio, the better. It is known that if the voltage holding ratio, which is one of the electrical characteristics of the liquid crystal display element, increases, line burn-in, which is one of the display defects of the liquid crystal display element, is less likely to occur. The evaluation was performed by defining a case where the voltage holding ratio was 75% or more as "verygood", a case where the voltage holding ratio was 50% or more and less than 75% as "good", and a case where the voltage holding ratio was less than 50% as "x".
< FFS drive liquid Crystal Box fabrication >
A liquid crystal cell having a fringe field switching (FRINGE FIELD SWITCHING: FFS) mode liquid crystal display element structure was fabricated.
First, a substrate with electrodes is prepared. The substrate was a glass substrate having a size of 30mm×35mm and a thickness of 0.7 mm. An ITO electrode having a planar pattern and constituting a counter electrode is formed as a first layer on a substrate. A SiN (silicon nitride) film formed by a CVD (chemical vapor deposition) method is formed as a second layer on the opposite electrode of the first layer. The SiN film of the second layer had a film thickness of 500nm, and comb-tooth-shaped pixel electrodes formed by patterning an ITO film were arranged as a third layer on the SiN film of the second layer, thereby forming two pixels, i.e., a first pixel and a second pixel. The size of each pixel is 10mm long and about 5mm wide. At this time, the counter electrode of the first layer and the pixel electrode of the third layer are electrically insulated by the SiN film of the second layer.
The pixel electrode of the third layer has a comb-tooth shape in which electrode elements of 3 μm width bent at an inner angle of 160 ° at a center portion are arranged in parallel at intervals of 6 μm, and one pixel has a first region and a second region with a line connecting bent portions of the electrode elements as a boundary.
When the first region and the second region of each pixel are compared, the electrode elements constituting the pixel electrodes are formed in different directions. That is, in the case of taking the rubbing direction of a liquid crystal alignment film to be described later as a reference, the electrode elements of the pixel electrode are formed so as to form an angle of +10° (clockwise) in the first region of the pixel, and the electrode elements of the pixel electrode are formed so as to form an angle of-10 ° (clockwise) in the second region of the pixel. That is, in the first region and the second region of each pixel, the directions of the rotation operation (in-plane switching: in-PLANE SWITCHING) of the liquid crystal in the substrate plane induced by the voltage application between the pixel electrode and the counter electrode are configured to be opposite to each other.
Next, the liquid crystal aligning agents AL-1 to AL-9 obtained in the above examples and comparative examples were filtered by a filter having a pore diameter of 1.0 μm, and then applied to the prepared electrode-equipped substrate and a glass substrate having a columnar spacer having a height of 4 μm and having an ITO film formed on the back surface thereof by spin coating. After drying on a heating plate at 80℃for 2 minutes, baking was performed for 20 minutes by using an infrared heating furnace at 230℃to obtain a polyimide film having a film thickness of 60 nm. The polyimide film was rubbed with a rayon cloth (roller diameter: 120mm, roller rotation speed: 500rpm, moving speed: 30mm/sec, pressing length: 0.3mm, rubbing direction: direction inclined by 10 ° with respect to the IZO comb electrodes of the third layer), then washed by ultrasonic irradiation in pure water for 1 minute, water droplets were removed by air blowing, and dried at 80℃for 10 minutes, to obtain a substrate with a liquid crystal alignment film. The two substrates with the liquid crystal alignment film are used as a group, and a sealant is printed on the substrates except for the liquid crystal injection port, and the other substrates are bonded so that the liquid crystal alignment film faces are opposite and the rubbing direction is antiparallel. Then, the sealant was cured to prepare an empty cell having a cell gap of 4 μm. The negative type liquid crystal MLC-7026-100 (manufactured by Merck) was injected into the empty cell by vacuum injection, and the injection port was sealed to obtain an FFS type liquid crystal cell. The resulting cell was then heated at 120℃for 1 hour and left at 23℃for one night for evaluation.
< Evaluation of residual shadows caused by long-term AC drive >)
Using the liquid crystal cell prepared as described above, an alternating voltage of 120 hours.+ -. 6V was applied at a frequency of 60Hz in a constant temperature environment of 60 ℃. Then, the liquid crystal cell was placed in a state where the pixel electrode and the counter electrode were short-circuited, and the liquid crystal cell was directly left at room temperature for one day.
After the liquid crystal cell was placed between two polarizers arranged with their polarization axes orthogonal to each other, the backlight was turned on in a state where no voltage was applied, and the arrangement angle of the liquid crystal cell was adjusted so that the brightness of the transmitted light became minimum. Then, the rotation angle at which the liquid crystal cell is rotated from the darkest angle of the second region of the first pixel to the darkest angle of the first region of the first pixel is calculated as an angle Δ. In the same manner, in the second pixel, the second region and the first region are compared, and the same angle Δ is calculated.
When the average value of the angle Δ of the first pixel and the angle Δ of the second pixel is smaller than 0.6 °, it is defined as "verygood" which is particularly excellent in the ghost characteristics, the average value of 0.6 ° or more and smaller than 1.0 ° is defined as "good", and the average value of 1.0 ° or more is defined as "×", and the evaluation is performed.
The results of the respective characteristic evaluations are shown in table 1.
TABLE 1
As shown in Table 1, when the liquid crystal aligning agents containing the hydroxyalkylamide compounds Add-1 to Add-2 as the component (B) of the present invention were used (examples 1 to 4), the rubbing resistance was excellent and the anisotropic performance was also good, as compared with the case of using the liquid crystal aligning agent containing no component (B) (comparative examples 1 to 5). Further, the sealing adhesion, voltage holding ratio, and residual image characteristics were also good.
Industrial applicability
The liquid crystal alignment film obtained from the liquid crystal alignment agent of the present invention can be applied to various liquid crystal display elements typified by IPS-mode liquid crystal display elements and FFS-mode liquid crystal display elements. The display elements are not limited to liquid crystal displays for display purposes, and may be used for liquid crystal alignment films for phase difference films, scanning antennas, liquid crystal alignment films for liquid crystal array antennas, or liquid crystal alignment films for transmission/scattering type liquid crystal light adjusting elements, or may be used for applications other than these, for example, protective films for color filters, gate insulating films for flexible displays, and substrate materials.
The entire contents of the specification, claims, drawings and abstract of japanese patent application 2020-189724, filed on 11/13/2020, are incorporated herein by reference as if disclosed in the specification of the present invention.
Claims (1)
1. A compound represented by the following formula (Add-1) or (Add-2),
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TW (1) | TW202225143A (en) |
WO (1) | WO2022102281A1 (en) |
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Publication number | Priority date | Publication date | Assignee | Title |
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JP6477039B2 (en) | 2014-12-22 | 2019-03-06 | Jsr株式会社 | Liquid crystal alignment agent, liquid crystal alignment film, and liquid crystal display element |
TWI770016B (en) * | 2016-03-30 | 2022-07-11 | 日商日產化學工業股份有限公司 | Liquid crystal alignment agent, liquid crystal alignment film and liquid crystal display element |
WO2020153659A1 (en) | 2019-01-21 | 2020-07-30 | 주식회사 엘지화학 | Liquid crystal alignment composition, and liquid crystal alignment film and liquid crystal display using same |
CN113423765B (en) * | 2019-02-27 | 2023-11-07 | 日产化学株式会社 | Liquid crystal aligning agent, liquid crystal alignment film, and liquid crystal display element using same |
WO2020184628A1 (en) | 2019-03-12 | 2020-09-17 | 日産化学株式会社 | Liquid crystal alignment agent, liquid crystal alignment film, and liquid crystal display element using same |
-
2021
- 2021-10-04 JP JP2022561322A patent/JP7318826B2/en active Active
- 2021-10-04 CN CN202410236258.5A patent/CN118108620A/en active Pending
- 2021-10-04 CN CN202180076210.7A patent/CN116529303B/en active Active
- 2021-10-04 WO PCT/JP2021/036656 patent/WO2022102281A1/en active Application Filing
- 2021-10-27 TW TW110139762A patent/TW202225143A/en unknown
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JPWO2022102281A1 (en) | 2022-05-19 |
TW202225143A (en) | 2022-07-01 |
JP7318826B2 (en) | 2023-08-01 |
WO2022102281A1 (en) | 2022-05-19 |
CN116529303A (en) | 2023-08-01 |
CN116529303B (en) | 2024-02-13 |
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