WO2013122257A1 - 圧電素子 - Google Patents
圧電素子 Download PDFInfo
- Publication number
- WO2013122257A1 WO2013122257A1 PCT/JP2013/054240 JP2013054240W WO2013122257A1 WO 2013122257 A1 WO2013122257 A1 WO 2013122257A1 JP 2013054240 W JP2013054240 W JP 2013054240W WO 2013122257 A1 WO2013122257 A1 WO 2013122257A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- glutamic acid
- copolymer
- methyl
- piezoelectric element
- Prior art date
Links
- -1 poly(α-amino acid) Polymers 0.000 claims abstract description 171
- JVEUTCWLEJSEDI-PXYINDEMSA-N (2s)-2,6-diamino-7-oxo-7-phenylmethoxyheptanoic acid Chemical group OC(=O)[C@@H](N)CCCC(N)C(=O)OCC1=CC=CC=C1 JVEUTCWLEJSEDI-PXYINDEMSA-N 0.000 claims abstract description 28
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 claims abstract description 17
- 235000013922 glutamic acid Nutrition 0.000 claims abstract description 17
- 239000004220 glutamic acid Substances 0.000 claims abstract description 17
- COLNVLDHVKWLRT-QMMMGPOBSA-N phenylalanine group Chemical group N[C@@H](CC1=CC=CC=C1)C(=O)O COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims abstract description 16
- 125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 claims abstract description 6
- 229920001577 copolymer Polymers 0.000 claims description 133
- 229960002989 glutamic acid Drugs 0.000 claims description 85
- KRKRAOXTGDJWNI-BKLSDQPFSA-N 4-methyl-L-glutamic acid Chemical compound OC(=O)C(C)C[C@H](N)C(O)=O KRKRAOXTGDJWNI-BKLSDQPFSA-N 0.000 claims description 77
- 235000008206 alpha-amino acids Nutrition 0.000 claims description 63
- 150000001370 alpha-amino acid derivatives Chemical class 0.000 claims description 58
- 125000004432 carbon atom Chemical group C* 0.000 claims description 44
- ATCFYQUZTYQTJN-AXDSSHIGSA-N (2s)-2-amino-4-benzylpentanedioic acid Chemical compound OC(=O)[C@@H](N)CC(C(O)=O)CC1=CC=CC=C1 ATCFYQUZTYQTJN-AXDSSHIGSA-N 0.000 claims description 35
- 125000000217 alkyl group Chemical group 0.000 claims description 29
- 229920001400 block copolymer Polymers 0.000 claims description 23
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims description 20
- 239000000758 substrate Substances 0.000 claims description 18
- 239000010409 thin film Substances 0.000 claims description 16
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 12
- 125000005843 halogen group Chemical group 0.000 claims description 10
- 125000003545 alkoxy group Chemical group 0.000 claims description 9
- 229910052731 fluorine Inorganic materials 0.000 claims description 9
- 125000001153 fluoro group Chemical group F* 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 229960005190 phenylalanine Drugs 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 7
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
- 229920005604 random copolymer Polymers 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 6
- 125000002723 alicyclic group Chemical group 0.000 claims description 5
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 5
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 claims description 5
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 5
- 229960003767 alanine Drugs 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 3
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 claims description 3
- QNAYBMKLOCPYGJ-UWTATZPHSA-N L-Alanine Natural products C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 229940049906 glutamate Drugs 0.000 claims description 3
- 229930195712 glutamate Natural products 0.000 claims description 3
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 2
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 claims description 2
- 239000002904 solvent Substances 0.000 abstract description 14
- 238000000034 method Methods 0.000 description 52
- 230000015572 biosynthetic process Effects 0.000 description 44
- 238000003786 synthesis reaction Methods 0.000 description 41
- 239000000203 mixture Substances 0.000 description 39
- 238000000691 measurement method Methods 0.000 description 31
- 239000010408 film Substances 0.000 description 23
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
- 229920000642 polymer Polymers 0.000 description 14
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-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
- 238000005809 transesterification reaction Methods 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 10
- 239000003999 initiator Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 238000011156 evaluation Methods 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 8
- 238000007639 printing Methods 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 238000005259 measurement Methods 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 230000005684 electric field Effects 0.000 description 6
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 6
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 6
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
- BESYJTGVSRKLNB-BKLSDQPFSA-N [(3s)-5-methyl-2,6-dioxooxan-3-yl]carbamic acid Chemical compound CC1C[C@H](NC(O)=O)C(=O)OC1=O BESYJTGVSRKLNB-BKLSDQPFSA-N 0.000 description 5
- 150000001371 alpha-amino acids Chemical class 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 229920000139 polyethylene terephthalate Polymers 0.000 description 5
- 239000005020 polyethylene terephthalate Substances 0.000 description 5
- 238000004528 spin coating Methods 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 229940024606 amino acid Drugs 0.000 description 4
- 235000001014 amino acid Nutrition 0.000 description 4
- 150000001413 amino acids Chemical class 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 238000005266 casting Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 150000004985 diamines Chemical group 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 125000000291 glutamic acid group Chemical group N[C@@H](CCC(O)=O)C(=O)* 0.000 description 4
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 4
- 125000006606 n-butoxy group Chemical group 0.000 description 4
- 125000001298 n-hexoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 4
- 239000003505 polymerization initiator Substances 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- BYEAHWXPCBROCE-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-ol Chemical compound FC(F)(F)C(O)C(F)(F)F BYEAHWXPCBROCE-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
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 3
- 239000002033 PVDF binder Substances 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 238000005227 gel permeation chromatography Methods 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 229940095102 methyl benzoate Drugs 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- DTQVDTLACAAQTR-DYCDLGHISA-N trifluoroacetic acid-d1 Chemical compound [2H]OC(=O)C(F)(F)F DTQVDTLACAAQTR-DYCDLGHISA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- WHBMMWSBFZVSSR-UHFFFAOYSA-N 3-hydroxybutyric acid Chemical compound CC(O)CC(O)=O WHBMMWSBFZVSSR-UHFFFAOYSA-N 0.000 description 2
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 241000282994 Cervidae Species 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- ZGEYCCHDTIDZAE-BYPYZUCNSA-N L-glutamic acid 5-methyl ester Chemical compound COC(=O)CC[C@H](N)C(O)=O ZGEYCCHDTIDZAE-BYPYZUCNSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- SGACESRWWGWYIE-AXDSSHIGSA-N [(3s)-5-benzyl-2,6-dioxooxan-3-yl]carbamic acid Chemical compound O=C1OC(=O)[C@@H](NC(=O)O)CC1CC1=CC=CC=C1 SGACESRWWGWYIE-AXDSSHIGSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- XSIFPSYPOVKYCO-UHFFFAOYSA-N butyl benzoate Chemical compound CCCCOC(=O)C1=CC=CC=C1 XSIFPSYPOVKYCO-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 239000011889 copper foil Substances 0.000 description 2
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 229920002313 fluoropolymer Polymers 0.000 description 2
- 239000004811 fluoropolymer Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 2
- 238000007641 inkjet printing Methods 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 125000006328 iso-butylcarbonyl group Chemical group [H]C([H])([H])C([H])(C(*)=O)C([H])([H])[H] 0.000 description 2
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 229910052451 lead zirconate titanate Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000003935 n-pentoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 2
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000006252 n-propylcarbonyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C(*)=O 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- 125000005920 sec-butoxy group Chemical group 0.000 description 2
- UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 2
- HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical compound CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 description 2
- 125000006253 t-butylcarbonyl group Chemical group [H]C([H])([H])C(C(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 2
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 2
- YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- BGGHCRNCRWQABU-JTQLQIEISA-N (2s)-2-amino-5-oxo-5-phenylmethoxypentanoic acid Chemical compound OC(=O)[C@@H](N)CCC(=O)OCC1=CC=CC=C1 BGGHCRNCRWQABU-JTQLQIEISA-N 0.000 description 1
- RFWFOJDAIRDAPK-VKHMYHEASA-N (3s)-3-aminooxane-2,6-dione Chemical compound N[C@H]1CCC(=O)OC1=O RFWFOJDAIRDAPK-VKHMYHEASA-N 0.000 description 1
- XZNOAVNRSFURIR-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-ol Chemical compound FC(F)(F)C(O)(C(F)(F)F)C(F)(F)F XZNOAVNRSFURIR-UHFFFAOYSA-N 0.000 description 1
- FQDXJYBXPOMIBX-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoro-2-methylpropan-2-ol Chemical compound FC(F)(F)C(O)(C)C(F)(F)F FQDXJYBXPOMIBX-UHFFFAOYSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 description 1
- JITSWUFGPFIMFG-UHFFFAOYSA-N 1,1,2,2,4-pentachlorobutane Chemical compound ClCCC(Cl)(Cl)C(Cl)Cl JITSWUFGPFIMFG-UHFFFAOYSA-N 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- KXJGSNRAQWDDJT-UHFFFAOYSA-N 1-acetyl-5-bromo-2h-indol-3-one Chemical compound BrC1=CC=C2N(C(=O)C)CC(=O)C2=C1 KXJGSNRAQWDDJT-UHFFFAOYSA-N 0.000 description 1
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
- 125000003229 2-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000005916 2-methylpentyl group Chemical group 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- LWHKUVOYICRGGR-UHFFFAOYSA-N 3-bicyclo[2.2.1]heptanylmethanol Chemical compound C1CC2C(CO)CC1C2 LWHKUVOYICRGGR-UHFFFAOYSA-N 0.000 description 1
- 125000003469 3-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000005917 3-methylpentyl group Chemical group 0.000 description 1
- 125000004874 3-methylpentylcarbonyl group Chemical group CC(CCC(=O)*)CC 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- WSMQKESQZFQMFW-UHFFFAOYSA-N 5-methyl-pyrazole-3-carboxylic acid Chemical compound CC1=CC(C(O)=O)=NN1 WSMQKESQZFQMFW-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- FMNPAGAVJLRACR-UHFFFAOYSA-N C[Si](C)(C)Cl.S(=O)(=O)(C(F)(F)F)[O-].C1(=CC=CC=C1)[NH2+]C1=CC=CC=C1 Chemical compound C[Si](C)(C)Cl.S(=O)(=O)(C(F)(F)F)[O-].C1(=CC=CC=C1)[NH2+]C1=CC=CC=C1 FMNPAGAVJLRACR-UHFFFAOYSA-N 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- 229910013641 LiNbO 3 Inorganic materials 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- XLBVNMSMFQMKEY-BYPYZUCNSA-N N-methyl-L-glutamic acid Chemical compound CN[C@H](C(O)=O)CCC(O)=O XLBVNMSMFQMKEY-BYPYZUCNSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229910004354 OF 20 W Inorganic materials 0.000 description 1
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 208000004210 Pressure Ulcer Diseases 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical compound OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 description 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000003254 anti-foaming effect Effects 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229910002113 barium titanate Inorganic materials 0.000 description 1
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 1
- 238000009530 blood pressure measurement Methods 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 239000004643 cyanate ester Substances 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- SSJXIUAHEKJCMH-UHFFFAOYSA-N cyclohexane-1,2-diamine Chemical compound NC1CCCCC1N SSJXIUAHEKJCMH-UHFFFAOYSA-N 0.000 description 1
- VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 1
- 125000006547 cyclononyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 229920000359 diblock copolymer Polymers 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- AZDCYKCDXXPQIK-UHFFFAOYSA-N ethenoxymethylbenzene Chemical compound C=COCC1=CC=CC=C1 AZDCYKCDXXPQIK-UHFFFAOYSA-N 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 125000004672 ethylcarbonyl group Chemical group [H]C([H])([H])C([H])([H])C(*)=O 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229920002457 flexible plastic Polymers 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- VBZWSGALLODQNC-UHFFFAOYSA-N hexafluoroacetone Chemical compound FC(F)(F)C(=O)C(F)(F)F VBZWSGALLODQNC-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 230000009878 intermolecular interaction Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- HFGPZNIAWCZYJU-UHFFFAOYSA-N lead zirconate titanate Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ti+4].[Zr+4].[Pb+2] HFGPZNIAWCZYJU-UHFFFAOYSA-N 0.000 description 1
- 238000007644 letterpress printing Methods 0.000 description 1
- GQYHUHYESMUTHG-UHFFFAOYSA-N lithium niobate Chemical compound [Li+].[O-][Nb](=O)=O GQYHUHYESMUTHG-UHFFFAOYSA-N 0.000 description 1
- 239000006166 lysate Substances 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- 125000005439 maleimidyl group Chemical class C1(C=CC(N1*)=O)=O 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- XMYQHJDBLRZMLW-UHFFFAOYSA-N methanolamine Chemical compound NCO XMYQHJDBLRZMLW-UHFFFAOYSA-N 0.000 description 1
- 229940087646 methanolamine Drugs 0.000 description 1
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 description 1
- 238000000813 microcontact printing Methods 0.000 description 1
- 238000001053 micromoulding Methods 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- DILRJUIACXKSQE-UHFFFAOYSA-N n',n'-dimethylethane-1,2-diamine Chemical compound CN(C)CCN DILRJUIACXKSQE-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000006610 n-decyloxy group Chemical group 0.000 description 1
- 125000006609 n-nonyloxy group Chemical group 0.000 description 1
- 125000006608 n-octyloxy group Chemical group 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000005246 nonafluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 108700024573 poly-gamma-benzyl-L-glutamate Proteins 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- UKDIAJWKFXFVFG-UHFFFAOYSA-N potassium;oxido(dioxo)niobium Chemical compound [K+].[O-][Nb](=O)=O UKDIAJWKFXFVFG-UHFFFAOYSA-N 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011863 silicon-based powder Substances 0.000 description 1
- 238000002174 soft lithography Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- NLDYACGHTUPAQU-UHFFFAOYSA-N tetracyanoethylene Chemical group N#CC(C#N)=C(C#N)C#N NLDYACGHTUPAQU-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- SYRHIZPPCHMRIT-UHFFFAOYSA-N tin(4+) Chemical class [Sn+4] SYRHIZPPCHMRIT-UHFFFAOYSA-N 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 229920000428 triblock copolymer Polymers 0.000 description 1
- 125000006000 trichloroethyl group Chemical group 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/80—Constructional details
- H10N30/85—Piezoelectric or electrostrictive active materials
- H10N30/857—Macromolecular compositions
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/10—Alpha-amino-carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/04—Polyamides derived from alpha-amino carboxylic acids
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/01—Manufacture or treatment
- H10N30/06—Forming electrodes or interconnections, e.g. leads or terminals
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N30/00—Piezoelectric or electrostrictive devices
- H10N30/01—Manufacture or treatment
- H10N30/09—Forming piezoelectric or electrostrictive materials
- H10N30/098—Forming organic materials
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/42—Piezoelectric device making
Definitions
- the present invention relates to a piezoelectric element containing a specific poly ⁇ -amino acid.
- printable electronics The technology for producing devices on a flexible substrate by printing is called printable electronics, which is one of the next-generation key technologies.
- technological development from various viewpoints has been actively studied.
- technological development has been attempted with drive elements, illumination elements, display elements, etc., and the realization of printing devices has entered the field of view.
- the present situation is that there is no suitable material for piezoelectric elements, and sufficient technical development has not been made.
- Piezoelectric element is an element that converts applied force into voltage or converts voltage into force.
- thin films of fluoropolymers such as polyvinylidene fluoride (PVDF) and vinylidene fluoride-trifluoroethylene copolymer (P (VDF / TrFE)) have often been used for piezoelectric elements.
- PVDF polyvinylidene fluoride
- P (VDF / TrFE) vinylidene fluoride-trifluoroethylene copolymer
- the fluoropolymer has poor film-forming properties, there are problems in uniformity of film thickness and smoothness of the film surface. Further, in order to obtain high piezoelectricity, stretching and polarization are required, and there is a problem that the cost is high and the usable processes are limited.
- Patent Document 1 describes that a poly ⁇ -amino acid in a helix form can be used as a piezoelectric material without any special treatment.
- Patent Document 2 proposes a piezoelectric polymer obtained from poly ⁇ -amino acid.
- Patent Document 1 does not describe poly- ⁇ -amino acids whose piezoelectricity was specifically measured, and poly- ⁇ -benzyl-L-glutamate specifically described in Patent Documents 1 and 2.
- poly ⁇ -amino acid composed of poly- ⁇ -methyl-L-glutamate is not sufficient in piezoelectricity and can only be dissolved in a specific solvent, and can be dissolved in various solvents and resins. The required printable material could not be used.
- An object of the present invention is to provide a poly ⁇ -amino acid which can be dissolved in various solvents and has excellent piezoelectricity, and to provide a piezoelectric element containing the same.
- R 2 is an unsubstituted alkyl group having 6 to 18 carbon atoms, or a substituted alkyl group having 1 to 6 carbon atoms in which part or all of the hydrogen atoms are substituted with a fluorine atom or a norbornyl group
- R 4 is an alkoxy group having 1 to 6 carbon atoms, an alkyl group having 1 to 12 carbon atoms in which some or all of the hydrogen atoms are substituted with fluorine atoms, or an alkyl group having 3 to 9 carbon atoms
- R 4 is a methoxy group, a butoxy group, a hexyloxy group, an n-hexylcarbonyl group, or a trifluoromethyl group.
- the polyamino acid is ⁇ -methyl-L-glutamic acid / ⁇ -hexyl-L-glutamic acid copolymer, ⁇ -methyl-L-glutamic acid / ⁇ -dodecyl-L-glutamic acid copolymer, ⁇ -benzyl-L-glutamic acid / ⁇ -dodecyl-L-glutamic acid copolymer, ⁇ -methyl-L-glutamic acid / ⁇ -hexadecyl-L-glutamic acid copolymer, ⁇ -methyl-L-glutamic acid / ⁇ -2,2,2-trifluoroethyl- L-glutamic acid copolymer, ⁇ -methyl-L-glutamic acid / ⁇ -2-norbornylmethyl-L-glutamic acid copolymer, ⁇ -benzyl-L-glutamic acid / ⁇ -2-norbornylmethyl-L-glutamic acid copolymer
- Mw weight average molecular weight
- a poly ⁇ -amino acid having excellent piezoelectricity can be provided, and an inexpensive and flexible piezoelectric element can be provided by printing.
- piezoelectricity means a property of generating electric charges by applying force or strain.
- a piezoelectric body means a substance exhibiting piezoelectricity.
- the electromotive force means a difference in potential that generates a current
- the maximum electromotive force means a maximum value of the electromotive force generated when a force is applied to the piezoelectric body.
- the electric field means a state of a space where voltage is applied, and the strength can be obtained by dividing the voltage by the thickness of the film.
- the piezoelectric element means an element using piezoelectricity that converts a force applied to a piezoelectric body into a voltage or converts a voltage into a force.
- the poly ⁇ -amino acid used in the present invention comprises (A) a glutamic acid ⁇ -ester unit represented by formula (I); (B) a glutamic acid ⁇ -ester unit represented by formula (II); 1 unit or more selected from the alanine unit, phenylalanine unit and N ⁇ -benzyloxycarbonyl lysine unit represented by the formula (IV), and the glutamic acid ⁇ -ester unit represented by the formula (IV).
- the unit (A) is a glutamic acid ⁇ -ester unit represented by the formula (I).
- R 1 represents a methyl group or a benzyl group.
- the unit of (A) is a glutamic acid ⁇ -methyl ester unit
- R 1 is a benzyl group
- the unit of (A) is a glutamic acid ⁇ -benzyl ester unit.
- R 1 is preferably a benzyl group.
- the unit of (B) includes (B) a glutamic acid ⁇ -ester unit represented by formula (II), an alanine unit represented by formula (III), a phenylalanine unit and an N ⁇ -benzyloxycarbonyl lysine unit, and a formula ( IV) one or more selected from glutamic acid ⁇ -ester units represented by IV).
- R 2 is an unsubstituted alkyl group having 6 to 18 carbon atoms, or a carbon in which some or all of the hydrogen atoms are substituted with a halogen atom or an alicyclic hydrocarbon group having 3 to 12 carbon atoms. It represents a substituted alkyl group having a number of 1 to 6. In view of excellent solubility, R 2 is preferably an unsubstituted alkyl group having 6 to 18 carbon atoms.
- the unsubstituted alkyl group having 6 to 18 carbon atoms in R 2 is a linear or branched alkyl group such as an n-hexyl group, an n-heptyl group, n-octyl group, n-nonyl group, n-decyl group, n-undecyl group, n-dodecyl group, n-tridecyl group, n-tetradecyl group, n-pentadecyl group, n-hexadecyl group, n-heptadecyl group, n-octadecyl group, 3-ethylbutyl group, 4-ethylbutyl group, 2-methylpentyl group, 3-methylpentyl group, 4-methylpentyl group, 5-methylpentyl group, 2-methylhexyl group, 3-methylhexyl group 4-methylhexyl group
- a linear alkyl group is preferable, and carbon A linear alkyl group having 6 to 16 carbon atoms is more preferable, and a linear alkyl group having 6 to 12 carbon atoms (that is, an n-hexyl group, an n-heptyl group, an n-octyl group, an n-nonyl group, n-decyl group, n-undecyl group, or n-dodecyl group) is more preferable, and n-hexyl group or n-dodecyl group is more preferable.
- alkyl group of 6 to 6 is a linear or branched alkyl group, for example, methyl group, ethyl group, n-propyl group, n-butyl group, n-pentyl group, n-hexyl group, isopropyl group. , Sec-butyl group, tert-butyl group, 2-methylbutyl group, and 3-ethylbutyl group.
- a methyl group having 1 to 3 carbon atoms, an ethyl group, an n-propyl group, or an isopropyl group is preferable, and a methyl group having 1 to 2 carbon atoms or an ethyl group is more preferable.
- the “alicyclic hydrocarbon group having 3 to 12 carbon atoms” may be a saturated hydrocarbon group or an unsaturated hydrocarbon group, but is preferably a saturated hydrocarbon group such as cyclopropyl group, cyclobutyl group, cyclopentyl.
- halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom, and among them, a fluorine atom is preferable.
- R 2 include n-hexyl group, n-dodecyl group, n-hexadecyl group, 2-norbornylmethyl group, and 2,2,2-trifluoroethyl group.
- R 3 represents a methyl group, a benzyl group or a (CH 2 ) 4 —NHZ group (in the group, Z represents a benzyloxycarbonyl group; the same shall apply hereinafter).
- the unit of (B) is an alanine unit
- R 3 is a benzyl group
- the unit of (B) is a phenylalanine unit
- R 3 is (CH 2 ) 4 -NHZ.
- the unit of (B) is a unit of N ⁇ -benzyloxycarbonyl lysine.
- a unit of N ⁇ -benzyloxycarbonyl lysine (unit of R 3 being (CH 2 ) 4 —NHZ group (wherein Z represents a benzyloxycarbonyl group)) is preferable.
- R 4 represents an alkoxy group having 1 to 12 carbon atoms, an alkyl group having 1 to 12 carbon atoms in which some or all of the hydrogen atoms are substituted with halogen atoms, or an alkyl group having 1 to 2 carbon atoms. 12 alkylcarbonyl groups are represented.
- the alkoxy group having 1 to 12 carbon atoms in R 4 in the formula (IV) is a linear or branched alkoxy group such as a methoxy group, an ethoxy group, an n-propoxy group, an n-butoxy group, n-pentyloxy group, n-hexyloxy group, n-heptyloxy group, n-octyloxy group, n-nonyloxy group, n-decyloxy group, n-undecyloxy group, n-dodecyloxy group, isopropoxy group , Sec-butoxy group, tert-butoxy group, 2-ethylhexyloxy group, and tert-octyloxy group.
- an alkoxy group having 1 to 6 carbon atoms that is, methoxy group, ethoxy group, n-propoxy group, n-butoxy group, n-pentyloxy group, n-hexyloxy group, isopropoxy group, sec-butoxy Group or a tert-butoxy group is preferable, and a methoxy group, an n-butoxy group, or an n-hexyloxy group is more preferable.
- the alkyl group having 1 to 12 carbon atoms in which part or all of the hydrogen atoms in R 4 are substituted with a halogen atom is a linear or branched alkyl group, and the halogen atom includes a fluorine atom, A chlorine atom, a bromine atom, and an iodine atom are mentioned, Preferably a fluorine atom is mentioned.
- halogen-substituted alkyl group examples include a monofluoromethyl group, a difluoromethyl group, a trifluoromethyl group, a trifluoroethyl group, a trifluorodimethylethyl group, a hexafluoroisopropyl group, a pentafluoroethyl group, a trifluorobutyl group, Pentafluorobutyl group, heptafluorobutyl group, nonafluorobutyl group, trifluoropentyl group, trifluoroheptyl group, trifluorooctyl group, trifluorononyl group, trifluorodecyl group, trifluoroundecyl group, trifluorododecyl group , Pentafluoropentyl group, heptafluoropentyl group, octafluoropentyl group, nonafluoropent
- the alkylcarbonyl group having 1 to 12 carbon atoms in R 4 is linear or branched, and includes, for example, methylcarbonyl, ethylcarbonyl, n-propylcarbonyl, isopropylcarbonyl, n-butylcarbonyl , Isobutylcarbonyl, tert-butylcarbonyl, sec-butylcarbonyl, n-pentylcarbonyl, isopentylcarbonyl, neopentylcarbonyl, n-hexylcarbonyl, isohexylcarbonyl, 3-methylpentylcarbonyl, n-heptylcarbonyl, n-octyl Mention may be made of carbonyl, n-nonylcarbonyl, n-decylcarbonyl, n-undecylcarbonyl and n-dodecylcarbonyl.
- n-propylcarbonyl isopropylcarbonyl, n-butylcarbonyl, isobutylcarbonyl, tert-butylcarbonyl, sec-butylcarbonyl, n-pentylcarbonyl, isopentylcarbonyl, wherein the alkyl group has 3 to 9 carbon atoms
- Neopentylcarbonyl, n-hexylcarbonyl, isohexylcarbonyl, n-heptylcarbonyl, or n-octylcarbonyl is preferred, and n-hexylcarbonyl is more preferred.
- R 4 include an alkoxy group having 1 to 6 carbon atoms, an alkyl group having 1 to 12 carbon atoms in which some or all of the hydrogen atoms are substituted with fluorine atoms, or the number of carbon atoms in the alkyl group. Examples thereof include 3 to 9 alkylcarbonyl groups. Particularly preferred examples of R 4 include a methoxy group, n-butoxy group, n-hexyloxy group, trifluoromethyl group, or n-hexylcarbonyl group.
- L in the formula (IV) represents an integer of 6 to 12, preferably an integer of 6 to 10.
- M represents an integer of 1 to 3, preferably 1 or 2, and when m is 2 or 3, two or three R 4 may be the same or different, but may be the same. preferable.
- the poly ⁇ -amino acid of the present invention is preferably a ⁇ -methyl-L-glutamic acid / ⁇ -hexyl-L-glutamic acid copolymer, a ⁇ -methyl-L-glutamic acid / ⁇ -dodecyl-L-glutamic acid copolymer, ⁇ -benzyl-L-glutamic acid / ⁇ -dodecyl-L-glutamic acid copolymer, ⁇ -methyl-L-glutamic acid / ⁇ -hexadecyl-L-glutamic acid copolymer, ⁇ -methyl-L-glutamic acid / ⁇ -2, 2,2-trifluoroethyl-L-glutamic acid copolymer, ⁇ -methyl-L-glutamic acid / ⁇ -2-norbornylmethyl-L-glutamic acid copolymer, ⁇ -benzyl-L-glutamic acid / ⁇ -2 -Norborn
- ⁇ -methyl-L-glutamic acid / ⁇ -hexyl-L-glutamic acid copolymer ⁇ -methyl-L-glutamic acid / ⁇ -dodecyl-L-glutamic acid copolymer, ⁇ -benzyl-L-glutamic acid / ⁇ -dodecyl-L-glutamic acid copolymer, ⁇ -methyl-L-glutamic acid / ⁇ -hexadecyl-L-glutamic acid copolymer, ⁇ -methyl-L-glutamic acid / ⁇ -2-norbornylmethyl-L-glutamic acid Copolymer, ⁇ -benzyl-L-glutamic acid / ⁇ -2-norbornylmethyl-L-glutamic acid copolymer, or ⁇ -methyl-L-glutamic acid / N ⁇ -benzyloxycarbonyl-L-lysine copolymer It is.
- the ⁇ -amino acids constituting the units of the formulas (I) to (IV) may be either L-form or D-form, but are preferably L-form because they are inexpensive. is there.
- the unit (A) may be one type or a plurality of types. Further, the unit of (B) may be one type or a plurality of types. Further, the formulas (I) to (IV) as the unit of (B) may be one kind or plural kinds.
- the N-terminus may be a unit (A) or a unit (B). An initiator may or may not be bonded to the terminal.
- the block consisting of the unit of (A) and the unit of the unit of (B) The block copolymer containing the block which becomes.
- the poly ⁇ -amino acid comprises units of formula (I) and units of formula (II) and / or (IV)
- a random copolymer is preferred.
- the poly ⁇ -amino acid comprises a unit of formula (I) and a unit of formula (III)
- either a random copolymer or a block copolymer may be used, but a block copolymer is preferable.
- the block copolymer a diblock copolymer and a triblock copolymer are preferable.
- the content of the unit (A) in all units of the poly ⁇ -amino acid varies depending on the type of the unit (B), but is preferably 0.01 mol% to 90 mol%.
- the upper limit is preferably 85 mol%, more preferably 80 mol%, and even more preferably 60 mol%.
- the lower limit is preferably 0.1 mol%, more preferably 1 mol%, still more preferably 5 mol%, still more preferably 10 mol%, still more preferably 15 mol%, still more preferably 20 mol%, and 40 mol%. Is more preferable.
- the content of the unit (B) in all the units of the poly ⁇ -amino acid varies depending on the type of the unit (B), but is preferably 10 mol% to 99.99 mol%.
- the upper limit is preferably 99.9 mol%, more preferably 99 mol%, further preferably 95 mol%, further preferably 90 mol%, further preferably 85 mol%, further preferably 80 mol%, and 60 mol%. Is even more preferred.
- the lower limit is more preferably 15 mol%, further preferably 20 mol%, and still more preferably 40 mol%.
- the unit of (B) is a unit of formula (IV)
- the lower limit is preferably 50 mol%, more preferably 60 mol%, and even more preferably 80 mol%.
- poly ⁇ -amino acid comprising the unit of formula (I) and the unit of formula (II)
- examples of the poly ⁇ -amino acid include ⁇ -methyl-L-glutamic acid (15 to 85 mol%) / ⁇ -hexyl-L-glutamic acid (15 to 85 mol%) copolymer, ⁇ -methyl-L-glutamic acid (40-60 mol%) / ⁇ -dodecyl-L-glutamic acid (40-60 mol%) copolymer, ⁇ -benzyl-L-glutamic acid (40 ⁇ 60 mol%) / ⁇ -dodecyl-L-glutamic acid (40-60 mol%) copolymer, ⁇ -methyl-L-glutamic acid (15-85 mol%) / ⁇ -hexadecyl-L-glutamic acid (15-85) Mol%) copolymer, ⁇ -methyl-L-glutamic acid (30 to 70 mol%) / ⁇ -2,2,2-triflu
- poly ⁇ -amino acid comprising the unit of the formula (I) and the unit of the formula (III) include ⁇ -methyl-L-glutamic acid (20 to 80 mol%) / N ⁇ -benzyloxycarbonyl-L-lysine.
- the poly ⁇ -amino acid comprising the unit of the formula (I) and the unit of the formula (II) and the formula (III) includes ⁇ -methyl-L-glutamic acid (20 to 30 mol%) / ⁇ -hexyl-L-glutamic acid. (20-30 mol%) / N ⁇ -benzyloxycarbonyl-L-lysine (40-60 mol%) copolymer.
- poly ⁇ -amino acid comprising the unit of formula (I) and the unit of formula (IV)
- examples of the poly ⁇ -amino acid comprising the unit of formula (I) and the unit of formula (IV) include, for example, ⁇ -methyl-L-glutamic acid ( ⁇ 1 mol%) / ⁇ - (6- (p-methoxyphenoxy) -1-hexyl) -L-glutamic acid (> 99 mol%) copolymer, ⁇ -methyl-L-glutamic acid ( ⁇ 1 mol%) / ⁇ - (6- (p-hexylcarbonylphenoxy) -1-hexyl) -L-glutamic acid (> 99 mol%) copolymer, ⁇ -methyl-L-glutamic acid ( ⁇ 1 mol to 16 mol%) / ⁇ - (10- (p-methoxyphenoxy) -1-decyl) -L- Glutamic acid (84 to> 99 mol%) copolymer, ⁇ -methyl
- the molecular weight of the poly ⁇ -amino acid is not particularly limited, but the weight average molecular weight (Mw) is 1,000 in order to obtain a piezoelectric property that is appropriately controlled by intermolecular interaction and suitable for film formation. ⁇ 5,000,000 is preferable, 5,000 to 2,500,000 is more preferable, and 10,000 to 2,000,000 is more preferable.
- the method for preparing the poly ⁇ -amino acid of the present invention is not particularly limited.
- An example is a method in which an anhydride or an N-carboxy- ⁇ -amino acid ester derivative anhydride is mixed as appropriate and dissolved or suspended in an organic solvent or water, and a polymerization initiator is added thereto as necessary for copolymerization. it can.
- N-carboxy- ⁇ -glutamic acid anhydride or N-carboxy- ⁇ -glutamic acid ⁇ -ester anhydride Dissolve or suspend the product in an organic solvent or water, add a polymerization initiator to this if necessary, polymerize it, prepare poly ⁇ -glutamic acid or poly ⁇ -glutamic acid ⁇ -ester, and then specify the raw material
- An appropriate amount of one or more alcohols is added to the glutamic acid unit of poly ⁇ -glutamic acid or poly ⁇ -glutamic acid ⁇ -ester, a catalyst is added if necessary, and an ester is introduced at the ⁇ position, or ⁇ position
- the method of preparing by converting ester of this can be mentioned.
- organic solvent examples include acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, tetrahydrofuran, diethyl ether, diisopropyl ether, petroleum ether, 1,4-dioxane, benzene, toluene, xylene, hexane, cyclohexane, ethyl acetate, butyl acetate.
- Trifluoroacetic acid Trifluoroacetic acid, acetic acid, formic acid, dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane, trichloroethane, trichloroethylene, trifluoroethane, 1,1,1,3,3,3-hexafluoro-2-propanol, 2,2,2-trifluoroethanol, hexafluoroacetone, methanol, ethanol, 1-propanol, 2-propanol, formamide, N, N-dimethylformamide, N, N-dimethyl Acetamide, N- methylpyrrolidone, dimethyl sulfoxide, pyridine, acetonitrile, may be mentioned trimethylamine, triethylamine, and tributylamine.
- One or more organic solvents can be used in combination.
- polymerization initiator examples include ethylenediamine, propylenediamine, hexamethylenediamine, 1,4-cyclohexanediamine, 1,2-cyclohexanediamine, o-phenylenediamine, m-phenylenediamine, p-phenylenediamine, and toluene-2.
- Primary amines such as methylamine, ethylamine, and 1-propylamine; alcohol amines such as methanolamine, ethanolamine, and diethanolamine; dimethylamine Secondary amines such as N, N-dimethylethylenediamine, and primary tertiary diamines such as N, N-dimethyl-1,3-propanediamine; Tertiary amines such as amine, triethylamine and tributylamine; amino group-containing polymers such as polyether diamine and polyester diamine; primary alcohols such as methanol and ethanol; secondary alcohols such as isopropanol; ethylene glycol, propylene glycol, 1 , 4-butanediol, and glycols such as hexamethylene glycol; hydroxyl group-containing polymers such as polyether diol and polyester diol; thiols and the like.
- One or more polymerization initiators can be used in combination.
- the catalyst examples include hydrochloric acid, sulfuric acid, nitric acid, p-toluenesulfonic acid, sodium hydroxide, potassium hydroxide, sodium methoxide, sodium t-butoxide, potassium methoxide, potassium t-butoxide, potassium cyanide, carbon dioxide, Mention may be made of titanium (IV) tetraisopropoxide, 1,3-substituted tetraalkyldistannoxane tin (IV) complexes, tetracyanoethylene, 4-dimethylaminopyridine, and diphenylammonium triflate-trimethylsilyl chloride.
- One or more catalysts can be used in combination.
- the amount of catalyst is appropriately set depending on the reaction, but in general, an appropriate reaction time can be realized and can be appropriately selected within the range where it is not difficult to remove the catalyst after the reaction.
- the number of moles of amino acid anhydride to be used 0.0001 to 1 equivalent, preferably 0.01 to 0.75 equivalent, and more preferably 0.1 to 0.5 equivalent.
- the amount of alcohol used as a raw material is appropriately set depending on the reaction, but in general, it can be appropriately selected within a range in which side chain conversion is sufficiently performed and removal of unreacted alcohol is not difficult. -0.01 to 50 equivalents, preferably 0.1 to 25 equivalents, more preferably 0.15 to 20 equivalents relative to the glutamic acid unit of the amino acid.
- the present invention provides a piezoelectric element containing the above poly ⁇ -amino acid.
- the poly ⁇ -amino acid is preferably made into a thin film and used as a piezoelectric film.
- the piezoelectric element has a poly ⁇ -amino acid piezoelectric film and an electrode on a substrate, preferably a flexible substrate.
- FIG. 1 shows a particularly preferred element.
- An element having a form in which a lower electrode 2, the above-described poly ⁇ -amino acid piezoelectric film 3 and an upper electrode 4 are sequentially laminated on a flexible substrate 1 is exemplified.
- the method for forming the poly ⁇ -amino acid piezoelectric film is not particularly limited, and any method may be used. Spin coating, dip coating, and casting are often used conveniently, but from the viewpoint of pattern control, screen printing, gravure printing, offset using ink containing poly ⁇ -amino acid Printing techniques such as printing, flexographic printing, and ink jet printing can also be used. Also, a printing method called soft lithography such as microcontact printing or micromolding can be applied.
- it can be formed by forming a polymer solution (poly ⁇ -amino acid-containing ink) in which poly ⁇ -amino acid is dissolved in an appropriate organic solvent into a thin film by spin coating or casting and drying the solution.
- the drying method is not particularly limited, and various methods such as drying by standing treatment and drying by an air dryer can be used.
- Various organic solvents can be used for spin coating and casting, for example, nitrogen-containing polar solvents such as N-methylpyrrolidone, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, dimethyl sulfone.
- Sulfoxide / sulfone solvents such as acetone, methyl ethyl ketone, diethyl ketone, acetophenone, cyclohexanone and other ketone solvents, dimethyl ether, dipropyl ether, tetrahydrofuran, triethylene glycol dimethyl ether and other ether solvents, methyl benzoate, benzoic acid ether, Benzoic acid ester solvents such as butyl benzoate, chloroform, methylene chloride, trichloroethylene, ethylene dichloride, dichloroethane, tetrachloroethane, chlorobenzene, etc.
- solvents such as acetone, methyl ethyl ketone, diethyl ketone, acetophenone, cyclohexanone and other ketone solvents, dimethyl ether, dipropyl ether, tetrahydrofuran, triethylene glycol dimethyl ether
- Halogen solvents methanol, ethanol, propanol, butanol, pentanol, ethylene glycol, propylene glycol, phenol, cresol, polyethylene glycol and other alcohol / phenol solvents, perfluoro-tert-butanol, hexafluoro-2-methylisopropanol, Examples thereof include fluorine-containing branched alcohol solvents such as 1,1,1,3,3,3-hexafluoroisopropanol, and aromatic hydrocarbon solvents such as benzene, toluene and xylene.
- the organic solvent one kind of solvent may be used alone, or two or more kinds thereof may be mixed and used.
- chloroform, 1,1,1,3,3,3-hexafluoroisopropanol, methylene chloride, dichloroethane, N-methylpyrrolidone, N, N-dimethylacetamide, methyl ethyl ketone, cyclohexanone, methyl benzoate, or toluene preferable.
- concentration of the solution (ink) is not particularly limited as long as uniform film formation can be achieved, but is preferably 1 to 50% (w / w), and 5 to 25% (w / w). preferable.
- the film forming temperature is not particularly limited, but is preferably 10 to 150 ° C, more preferably 20 to 100 ° C.
- the thickness of the piezoelectric film containing poly ⁇ -amino acid is preferably 500 nm to 500 ⁇ m, more preferably 1 to 100 ⁇ m, and even more preferably 10 to 80 ⁇ m.
- a composite piezoelectric film can be produced using the poly ⁇ -amino acid of the present invention and other materials having piezoelectricity, such as ceramic piezoelectric materials or organic piezoelectric materials.
- other materials having piezoelectricity such as ceramic piezoelectric materials or organic piezoelectric materials.
- a method of blending with a ceramic piezoelectric material or an organic piezoelectric material to form a thin film, or a method of laminating piezoelectric films can be mentioned.
- Ceramic piezoelectric materials include lead zirconate titanate (PZT), natural or artificial quartz, lithium niobate (LiNbO 3 ), potassium niobate tantalate [K (Ta, Nb) O 3 ], barium titanate (BaTiO 3 ). 3 ), lithium tantalate (LiTaO 3 ), and strontium titanate (SrTiO 3 ).
- Organic piezoelectric materials include cellulose acetate, cyanoethyl cellulose polypropylene oxide, poly ( ⁇ -hydroxybutyric acid), polyvinylidene fluoride, vinylidene fluoride-trifluoroethylene copolymer, vinylidene fluoride-tetrafluoroethylene copolymer, cyanide Examples include vinylidene-vinyl acetate copolymer and nylon 11.
- the composition of various ceramic materials and organic materials can be selected as appropriate in terms of performance.
- the poly ⁇ -amino acid of the present invention may optionally contain various resins and additives other than those described above as long as the effect as a piezoelectric film is exhibited.
- resin additives include inorganic fillers such as silica, talc, and barium sulfate, colorants such as pigments and dyes, organic fillers such as carbon black, silicon powder, nylon powder, and fluorine powder, and increases such as olben and benton.
- Adhesives silicone-based, fluorine-based, polymer-based antifoaming or leveling agents, silane coupling agents, epoxy resins, acrylic resins, phenolic resins, isocyanate resins, cyanate ester resins, and other thermosetting resins, triazole compounds, Examples thereof include adhesion imparting agents such as thiazole compounds, triazine compounds, and porphyrin compounds, rubber particles, maleimide compounds, bisallyl nadiimide compounds, vinyl benzyl resins, vinyl benzyl ether resins, and the like.
- the substrate is not particularly limited, glass substrate such as quartz, semiconductor substrate such as silicon wafer, hard plastic substrate such as paper epoxy, glass epoxy, flexible plastic substrate such as polycarbonate, polyimide, polyethylene terephthalate (PET), and Paper is an example.
- the material of the electrode is often a metal such as gold, silver, copper, or indium tin oxide (ITO), but is not limited thereto.
- the manufacturing method is not particularly limited, and any method may be used. Commonly used methods are photolithography from copper foil, plated wiring, etc., but wet manufacturing processes such as letterpress printing, screen printing, ink jet printing, and the like, which are applied or adhered, are also applicable.
- an electrode made of an organic material such as thiophene conductive polymer (PEDOT), polyaniline, and derivatives thereof can be used in addition to the silver paste. It is also possible to apply a dry manufacturing process different from the above, such as a vacuum evaporation method or a sputtering method.
- the electrode is formed of a mixture of a plurality of substances, has a layered structure of several substances, or is subjected to a surface treatment. It is also possible.
- the piezoelectric element of the present invention becomes an inexpensive and flexible piezoelectric element that has not been heretofore used, so that it is useful in the fields of pressure sensors, strain sensors, position sensors, speakers, microphones, measuring instruments, piezoelectric vibrators, actuators and the like.
- body pressure can be measured if placed along the surface of a load-bearing part such as a bed, mat, or chair (including sofas, wheelchairs, and seats of vehicles (including cars, railcars, and aircraft)). It becomes possible to prevent pressure ulcers.
- a foot pressure measurement sheet (a sheet that measures how much load is transferred to the ground by which part of the sole of the foot), and a tooth meshing measuring instrument (which is sandwiched between the upper and lower teeth and chewed) It is possible to construct a sheet-like pressure measuring instrument such as a sheet for measuring how much compressive load is applied to the object by the teeth.
- Step 1 Synthesis of ⁇ -methyl-L-glutamic acid / ⁇ -hexyl-L-glutamic acid copolymer (Step 1) Synthesis of poly- ⁇ -methyl-L-glutamic acid 410 ml of 1,2-dichloroethane (manufactured by Kanto Chemical Co., Inc.) ), N-carboxy- ⁇ -methyl-L-glutamic anhydride (54.92 g, 293.45 mmol) was added, cooled to 0 ° C., and N, N-dimethyl-1,3-propanediamine as an initiator (366 ⁇ l, 2.93 mmol, manufactured by Kanto Chemical Co., Inc.) was added, and the mixture was stirred at 25 ° C.
- Step 2 Side chain substitution reaction (transesterification reaction) of poly- ⁇ -methyl-L-glutamic acid 9.3 g of the poly- ⁇ -methyl-L-glutamic acid prepared above was dissolved in 45 ml of 1,2-dichloroethane, and 1-hexanol (16 ml, 130.00 mmol, manufactured by Tokyo Chemical Industry Co., Ltd.) and p-toluenesulfonic acid 1 Hydrate (1.24 g, 6.50 mmol, manufactured by Tokyo Chemical Industry Co., Ltd.) was added, and the mixture was stirred at 80 ° C.
- Synthesis Examples 2 to 3, 5 to 7, 9 to 14 Synthesis of various poly ⁇ -amino acids After obtaining poly- ⁇ -methyl-L-glutamic acid by the same method as in Synthesis Example 1, it was converted to 1,2-dichloroethane. Dissolve, add an appropriate amount of the alcohol shown in Table 1 (introduction alcohol column) to the glutamic acid unit of poly- ⁇ -methyl-L-glutamic acid, add a catalytic amount of p-toluenesulfonic acid monohydrate, Various poly ⁇ -amino acids (copolymers) were obtained by the procedure of stirring for 5 days.
- the weight average molecular weight Mw of the copolymer was measured by the following method (measurement method 1). Further, the composition of the polymer after the transesterification reaction was measured by the following method (Measurement Method 2).
- Synthesis Example 4 Synthesis of ⁇ -benzyl-L-glutamic acid / ⁇ -dodecyl-L-glutamic acid copolymer (Step 1) Synthesis of poly- ⁇ -benzyl-L-glutamic acid 265 ml of 1,2-dichloroethane (manufactured by Kanto Chemical Co., Inc.) ) With N-carboxy- ⁇ -benzyl-L-glutamic anhydride (44.2 g, 167.98 mmol) and N, N-dimethyl-1,3-propanediamine (208.2 ⁇ l, 1.68 mmol) as an initiator. In addition, the mixture was stirred at 25 ° C.
- Step 2 Side chain substitution reaction (transesterification reaction) of poly- ⁇ -benzyl-L-glutamic acid Poly- ⁇ -benzyl-L-glutamic acid (10 g, 45.6 mmol) prepared above was dissolved in 170 ml of 1,2-dichloroethane, 1-dodecanol (10.2 ml, 45.6 mmol, manufactured by Tokyo Chemical Industry Co., Ltd.) and p-Toluenesulfonic acid monohydrate (2.6 g, 13.68 mmol) was added, and the mixture was stirred at 65 ° C.
- the weight average molecular weight Mw of the copolymer was measured by the following method (measurement method 1). Further, the composition of the polymer after the transesterification reaction was measured by the following method (Measurement Method 2).
- Synthesis Example 8 Synthesis of ⁇ -benzyl-L-glutamic acid / ⁇ -2-norbornylmethyl-L-glutamic acid copolymer After obtaining poly- ⁇ -benzyl-L-glutamic acid by the same method as in Synthesis Example 4, It is dissolved in 1,2-dichloroethane, and an equivalent amount of norbornane-2-methanol (manufactured by Tokyo Chemical Industry Co., Ltd.) and a catalytic amount of p-toluenesulfonic acid per water with respect to the glutamic acid unit of poly- ⁇ -benzyl-L-glutamic acid. The hydrate was added and stirred at 65 ° C.
- the weight average molecular weight Mw of the copolymer was measured by the following method (measurement method 1). Further, the composition of the polymer after the transesterification reaction was measured by the following method (Measurement Method 2).
- Synthesis Example 15 Synthesis of ⁇ -methyl-L-glutamic acid / N ⁇ -benzyloxycarbonyl-L-lysine copolymer N ⁇ -carboxy-N ⁇ -benzyloxycarbonyl-L-lysine anhydrous in 130 ml of 1,2-dichloroethane Product (4.02 g, 13.12 mmol) and N-carboxy- ⁇ -methyl-L-glutamic anhydride (2.46 g, 13.12 mmol) were added, and N, N-dimethyl-1,3-propane was used as an initiator. Diamine (32.78 ⁇ l, 0.262 mmol) was added and stirred at 25 ° C.
- the weight average molecular weight Mw of the copolymer was measured by the following method (Measurement Method 1). Moreover, the composition of the copolymer was measured by the following method (measurement method 2).
- Synthesis Examples 16 to 19 Synthesis of various copolymers
- 1,2 dichloroethane was equimolar with two types of N-carboxy-L-amino acid anhydrides (component A and component B) shown in Table 2.
- 1/100 equivalent amount of N, N-dimethyl-1,3-propanediamine as an initiator was added to the amino acid anhydride and stirred for 2 to 3 days to obtain various polyamino acid copolymers.
- the weight average molecular weight Mw of the copolymer was measured by the following method (Measurement Method 1).
- the composition of the copolymer was measured by the following method (measurement method 2).
- Synthesis Example 21 Synthesis of ⁇ -methyl-L-glutamic acid (41%)- N ⁇ -benzyloxycarbonyl-L-lysine (18%)- ⁇ -methyl-L-glutamic acid (41%) block copolymer Synthesis Example After obtaining ⁇ -methyl-L-glutamic acid-N ⁇ -benzyloxycarbonyl-L-lysine block copolymer in the same manner as in No. 20, the mixture was again cooled to 0 ° C and 10 ml of 1,2-dichloroethane was added. , N-carboxy- ⁇ -methyl-L-glutamic anhydride (5.00 g, 26.72 mmol) was added and stirred at 25 ° C.
- Synthesis Examples 24 to 25 Synthesis of various poly ⁇ -amino acids N-carboxy- ⁇ -benzyl-L-glutamic acid anhydride and N ⁇ -carboxy-N ⁇ -benzyloxycarbonyl-L-lysine were prepared in the same manner as in Synthesis Example 22. An appropriate amount of anhydride was added to obtain various poly ⁇ -amino acid block copolymers (low molecular weight products).
- Synthesis Example 26 Synthesis of ⁇ -benzyl-L-glutamic acid (53%)-N ⁇ -benzyloxycarbonyl-L-lysine (47%) block copolymer (high molecular weight) N-to 10 ml of 1,2-dichloroethane Carboxy- ⁇ -benzyl-L-glutamic anhydride (1.00 g, 3.80 mmol) was added, and then cooled to 0 ° C., and N, N-dimethyl-1,3-propanediamine (0.48 ⁇ l) was used as an initiator. 3.8 ⁇ mol) was added, and the mixture was stirred at 25 ° C. for 1 day, then cooled to 0 ° C.
- Synthesis Example 27 ⁇ -Methyl-L-glutamic acid (25%) / ⁇ -hexyl-L-glutamic acid (25%)-N ⁇ -benzyloxycarbonyl-L-lysine (50%) block copolymer (Step 1) Synthesis of poly- ⁇ -methyl-L-glutamic acid (50%)-N ⁇ -benzyloxycarbonyl-L-lysine (50%) block copolymer Poly- ⁇ -methyl-L by the same method as in Synthesis Example 20 A glutamic acid (50%)- N ⁇ -benzyloxycarbonyl-L-lysine (50%) block copolymer was synthesized.
- the obtained block copolymer was measured for the weight average molecular weight Mw of the copolymer by the following method (measurement method 1). Moreover, the composition of the copolymer was measured by the following method (measurement method 2). (Step 2) Side chain of poly- ⁇ -methyl-L-glutamic acid in poly- ⁇ -methyl-L-glutamic acid (50%)-N ⁇ -benzyloxycarbonyl-L-lysine (50%) block copolymer Substitution reaction (transesterification reaction) 5.47 g of the poly- ⁇ -methyl-L-glutamic acid (50%)-N ⁇ -benzyloxycarbonyl-L-lysine (50%) block copolymer prepared above was dissolved in 25 ml of 1,2-dichloroethane, 1-hexanol (0.96 ml, 19.50 mmol, manufactured by Tokyo Chemical Industry Co., Ltd.) and p-toluenesulfonic acid monohydrate (0.075 g, 0.39
- the ester exchange reaction was carried out with stirring for a day to obtain a ⁇ -methyl-L-glutamic acid / ⁇ -hexyl-L-glutamic acid copolymer.
- the weight average molecular weight Mw of the copolymer was measured by the following method (measurement method 1). Further, the composition of the polymer after the transesterification reaction was measured by the following method (Measurement Method 2).
- the device shown in FIG. 1 was manufactured based on the following device manufacturing method.
- the poly ⁇ -amino acid thin film (piezoelectric film) was formed by a casting method.
- element fabrication method A polyethylene terephthalate (PET) substrate 1 (thickness: 125 ⁇ 5 ⁇ m) on which an ITO (indium tin oxide) electrode was deposited as the electrode 2 was washed with methanol.
- a polymer thin film was produced as a piezoelectric film 3 from a poly ⁇ -amino acid solution by a casting method.
- the thin film was sandwiched between PET substrates 4 on which ITO electrodes were deposited to produce an element.
- Table 5 shows the solvents and solution concentrations of the poly ⁇ -amino acid solutions of Synthesis Examples 1, 3, 4, 6, 7, 16, 20, 21, 22, and 26 used for forming the piezoelectric film, and after film formation. The film thickness is shown.
- Measuring method 1 Measuring method of weight average molecular weight
- the weight average molecular weight Mw was measured using gel permeation chromatography (GPC). Specifically, an analytical column device (Showa Denko, Shodex K-802 and K-806M) is attached to a GPC analyzer (Hitachi, LaChrom Elite), and 10-80 ⁇ l of a separately prepared measurement solution is injected. The eluent flow rate was 1 ml / min, the column retention temperature was 40 ° C., and the solvent was chloroform. The measurement solution was prepared by dissolving in chloroform so that the polyamino acid concentration was 0.25 to 3.0% (w / v), followed by filter filtration. The weight average molecular weight Mw was calculated by comparing the retention time of the obtained peak with the retention time of a separately measured polystyrene for calibration (Shodex STANDARD SM-105, manufactured by Showa Denko KK).
- Measurement method 2 Composition measurement method of copolymer after transesterification reaction After dissolving 10 mg of sample in deuterated chloroform or deuterated trifluoroacetic acid, 1 H nuclear magnetic resonance spectrum ( 1 HNMR, BRUKER, 400 MHz) was analyzed. The composition was calculated by comparing the peak areas of protons at the ⁇ -position of the amino acid before and after transesterification or during copolymerization. A measurement example is shown below.
- the composition of the copolymer is ⁇ -methyl-L-glutamic acid (39%) / ⁇ -hexyl-L-glutamic acid (61%).
- the composition of the copolymer is ⁇ -benzyl-L-glutamic acid (50%) / N ⁇ -benzyloxycarbonyl-L-lysine (50%). Become.
- Measurement Method 3 Evaluation Method of Piezoelectric Constant d33 Various synthesized polyamino acid solutions were applied to a copper foil (JX 35 ⁇ m, JX Nippon Mining & Metals Co., Ltd.) and then allowed to stand at room temperature for 12 hours or more and dried. This was cut into 1 cm square, and the value of the piezoelectric constant d33 was measured using a d33 meter (NPT22001T manufactured by Nippon Ferro Technology Co., Ltd.). At this time, the measurement was performed with the upper contact electrode 5 ⁇ and the load 150g.
- Evaluation Method 1 Evaluation of Piezoelectric Element An electromotive force generated when a load (about 6 kg) is applied to the produced element is measured at room temperature (20 ° C.) using a source meter manufactured by KEITHLEY, and the electric field is determined from the film thickness. The piezoelectric element was evaluated by determining the size of.
- the evaluation criteria are as follows. A: Electric field is 0.50 V / ⁇ m or more ⁇ : Electric field is 0.30 V / ⁇ m or more and less than 0.50 V / ⁇ m ⁇ : Electric field is 0.25 V / ⁇ m or more and less than 0.30 V / ⁇ m ⁇ : Electric field is 0.00. Less than 25V / ⁇ m
- the specific poly ⁇ -amino acid of the present invention can form a thin film with high uniformity of film thickness.
- the piezoelectricity was insufficient, but the specific poly ⁇ -amino acid thin film of the present invention was used. In the piezoelectric element, sufficient piezoelectricity was shown.
- Evaluation Method 2 Evaluation of Solubility in Solvents 20 parts by weight of the synthesized compound was added to 80 parts by weight of various solvents, and the resulting mixture was mixed at a ratio of 20 w% and stirred at room temperature to evaluate the solubility.
- the evaluation criteria are as follows. ⁇ : Completely soluble ⁇ : Partially soluble ⁇ : Insoluble
- the solvents used in the experiment are as follows. Dichloromethane: manufactured by Junsei Chemical Co., Ltd., special grade cyclohexanone: Tokyo Chemical Industry Co., Ltd. N, N-dimethylacetamide: produced by Kanto Chemical Co., Ltd., deer special grade methyl benzoate: produced by Kanto Chemical Co., Ltd., deer special grade toluene: produced by Junsei Chemical Co., Ltd. Triethylene glycol dimethyl ether): Nacalai Tesque
- a printable piezoelectric body can be provided, and a flexible piezoelectric element can be provided.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Polyamides (AREA)
Abstract
Description
[1]
(A)式(I)で表されるグルタミン酸γ−エステル単位:
式(I):
(式中、R1はメチル基またはベンジル基を表す。)と、
(B)式(II)で表されるグルタミン酸γ−エステル単位、式(III)で表されるアラニン単位、フェニルアラニン単位およびNε−ベンジルオキシカルボニルリジン単位、ならびに式(IV)で表されるグルタミン酸γ−エステル単位から選択される1種以上の単位:
式(II):
(式中、R2は炭素数が6~18の非置換のアルキル基、または、水素原子の一部もしくは全部がハロゲン原子もしくは炭素数が3~12の脂環式炭化水素基で置換された炭素数が1~6の置換アルキル基を表す。)
式(III):
(式中、R3はメチル基、ベンジル基または(CH2)4−NHZ基(基中、Zはベンジルオキシカルボニル基を表す。)を表す。)
式(IV):
(式中、R4は炭素数が1~12のアルコキシ基、水素原子の一部もしくは全部がハロゲン原子で置換された炭素数が1~12のアルキル基、または、アルキル基の炭素数が1~12のアルキルカルボニル基を表し、m個のR4は同一でも異なってもよい。lは6~12の整数、mは1~3の整数を表す。)
を含有するポリα−アミノ酸を含む圧電素子。
[2]
R2が炭素数6~18の非置換のアルキル基、または、水素原子の一部もしくは全部がフッ素原子もしくはノルボルニル基で置換された炭素数が1~6の置換アルキル基である上記[1]に記載の圧電素子。
[3]
R2がn−ヘキシル基、n−ドデシル基、n−ヘキサデシル基、2−ノルボニルメチル基または2,2,2−トリフルオロエチル基である上記[1]または[2]に記載の圧電素子。
[4]
R3が(CH2)4−NHZ基(基中、Zはベンジルオキシカルボニル基を表す)である上記[1]から[3]のいずれか一項に記載の圧電素子。
[5]
R4が炭素数が1~6のアルコキシ基、水素原子の一部もしくは全部がフッ素原子で置換された炭素数が1~12のアルキル基、または、アルキル基の炭素数が3~9のアルキルカルボニル基である上記[1]から[4]のいずれか一項に記載の圧電素子。
[6]
R4がメトキシ基、ブトキシ基、ヘキシルオキシ基、n−ヘキシルカルボニル基、またはトリフルオロメチル基である上記[1]から[5]のいずれか一項に記載の圧電素子。
[7]
ポリアミノ酸が、γ−メチル−L−グルタミン酸/γ−ヘキシル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−ドデシル−L−グルタミン酸共重合体、γ−ベンジル−L−グルタミン酸/γ−ドデシル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−ヘキサデシル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−2,2,2−トリフルオロエチル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−2−ノルボルニルメチル−L−グルタミン酸共重合体、γ−ベンジル−L−グルタミン酸/γ−2−ノルボルニルメチル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(6−(p−メトキシフェノキシ)−1−ヘキシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(6−(p−ヘキシルカルボニルフェノキシ)−1−ヘキシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(10−(p−メトキシフェノキシ)−1−デシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(6−(p−ブトキシフェノキシ)−1−ヘキシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(6−(p−ヘキシルオキシフェノキシ)−1−ヘキシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(6−(3,5−ビス(トリフルオロメチル)フェノキシ)−1−ヘキシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/Nε−ベンジルオキシカルボニル−L−リジン共重合体、γ−ベンジル−L−グルタミン酸/Nε−ベンジルオキシカルボニル−L−リジン共重合体、γ−メチル−L−グルタミン酸/L−フェニルアラニン共重合体、γ−ベンジル−L−グルタミン酸/L−フェニルアラニン共重合体、およびγ−ベンジル−L−グルタミン酸/L−アラニン共重合体から選択される1種以上である上記[1]記載の圧電素子。
[8]
ポリα−アミノ酸がランダム共重合体である上記[1]から[7]のいずれか一項に記載の圧電素子。
[9]
ポリα−アミノ酸がブロック共重合体である上記[1]から[7]のいずれか一項に記載の圧電素子。
[10]
ポリα−アミノ酸の重量平均分子量(Mw)が1,000~5,000,000であることを特徴とする上記[1]から[9]のいずれか一項に記載の圧電素子。
[11]
フレキシブル基板、電極、およびポリα−アミノ酸を有することを特徴とする上記[1]から[10]のいずれか一項に記載の圧電素子。
[12]
ポリα−アミノ酸が薄膜状であることを特徴とする上記[1]から[11]のいずれか一項に記載の圧電素子。
[13]
ポリα−アミノ酸の薄膜が500nm~500μmの薄膜状であることを特徴とする請求項[12]記載の圧電素子。
[14]
フレキシブル基板上に、下部電極、ポリα−アミノ酸、上部電極を積層させることを特徴とする上記[1]から[13]のいずれか一項に記載の圧電素子を製造する方法。
[15]
上記[1]から[13]のいずれか一項に記載の圧電素子を製造するための、ポリアミノ酸含有インク。
本発明に使用するポリα−アミノ酸は、(A)式(I)で表されるグルタミン酸γ−エステル単位と;(B)式(II)で表されるグルタミン酸γ−エステル単位、式(III)で表されるアラニン単位、フェニルアラニン単位およびNε−ベンジルオキシカルボニルリジン単位、ならびに式(IV)で表されるグルタミン酸γ−エステル単位から選択される1種以上の単位を含有する。
(A)の単位は、式(I)で表されるグルタミン酸γ−エステル単位である。
(B)の単位は、(B)式(II)で表されるグルタミン酸γ−エステル単位、式(III)で表されるアラニン単位、フェニルアラニン単位およびNε−ベンジルオキシカルボニルリジン単位、ならびに式(IV)で表されるグルタミン酸γ−エステル単位から選択される1種以上である。
より好ましくは、γ−メチル−L−グルタミン酸/γ−ヘキシル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−ドデシル−L−グルタミン酸共重合体、γ−ベンジル−L−グルタミン酸/γ−ドデシル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−ヘキサデシル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−2−ノルボルニルメチル−L−グルタミン酸共重合体、γ−ベンジル−L−グルタミン酸/γ−2−ノルボルニルメチル−L−グルタミン酸共重合体、またはγ−メチル−L−グルタミン酸/Nε−ベンジルオキシカルボニル−L−リジン共重合体である。
本発明は上記のポリα−アミノ酸を含む圧電素子を提供する。ポリα−アミノ酸を薄膜状にし、圧電体膜として使用することが好ましい。圧電素子は、基板上、好ましくはフレキシブル基板上に、ポリα−アミノ酸の圧電体膜、および電極を有する。
例えば、ベッド、マット、イス(ソファー、車イス、乗り物(自動車、鉄道車両、航空機など)の座席部をも含む)などの荷重を受ける部分の表層に沿って配置すれば、体圧の測定が可能となり褥瘡の防止などが可能となる。また、圧力センサーの数字を解析することで脈拍や呼吸などをセンシングすることが可能となり体調等をデータ化することが可能となる。また、足圧測定シート(足の裏のどの領域部分がどれほどの荷重を地面に伝えているかを測定するシート)、歯の噛み合わせ測定器(上下の歯の間に挟んで噛むことによって、どの歯がどれほどの圧縮荷重を対象物に作用させているかを測定するシート)など、シート状の圧力測定器を構成することが可能になる。
合成例1:γ−メチル−L−グルタミン酸/γ−ヘキシル−L−グルタミン酸共重合体の合成
(ステップ1)ポリ−γ−メチル−L−グルタミン酸の合成
1,2−ジクロロエタン410ml(関東化学社製)にN−カルボキシ−γ−メチル−L−グルタミン酸無水物(54.92g、293.45mmol)を入れた後、0℃まで冷却し、開始剤としてN,N−ジメチル−1,3−プロパンジアミン(366μl、2.93mmol、関東化学社製)を加え、25℃で1日間攪拌を行い、ポリ−γ−メチル−L−グルタミン酸を得た。下記の方法(測定法1)で重量平均分子量Mwを測定した。重量平均分子量Mwは1.9×104であった。
(ステップ2)ポリ−γ−メチル−L−グルタミン酸の側鎖置換反応(エステル交換反応)
上記で調製したポリ−γ−メチル−L−グルタミン酸9.3gを1,2−ジクロロエタン45mlに溶解させ、1−ヘキサノール(16ml、130.00mmol、東京化成工業社製)ならびにp−トルエンスルホン酸1水和物(1.24g、6.50mmol、東京化成工業社製)を加え、80℃で1日間攪拌してエステル交換反応を行い、γ−メチル−L−グルタミン酸/γ−ヘキシル−L−グルタミン酸共重合体を得た。得られた共重合体について、下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)でエステル交換反応後の重合体の組成を測定した。
合成例1と同様の方法により、ポリ−γ−メチル−L−グルタミン酸を得た後、1,2−ジクロロエタンに溶解させ、表1(導入アルコールの欄)に示すアルコールをポリ−γ−メチル−L−グルタミン酸のグルタミン酸単位に対して適量加え、触媒量のp−トルエンスルホン酸1水和物を加え、1~5日間攪拌を行う手順により、各種ポリα−アミノ酸(共重合体)を得た。得られた共重合体について、下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)でエステル交換反応後の重合体の組成を測定した。
(ステップ1)ポリ−γ−ベンジル−L−グルタミン酸の合成
1,2−ジクロロエタン265ml(関東化学社製)にN−カルボキシ−γ−ベンジル−L−グルタミン酸無水物(44.2g、167.98mmol)と開始剤としてN,N−ジメチル−1,3−プロパンジアミン(208.2μl、1.68mmol)を加え、25℃で3日間攪拌を行い、ポリ−γ−ベンジル−L−グルタミン酸を得た。下記の方法(測定法1)で重量平均分子量Mwを測定した。重量均分子量Mwは2.2×104であった。
(ステップ2)ポリ−γ−ベンジル−L−グルタミン酸の側鎖置換反応(エステル交換反応)
上記で調製したポリ−γ−ベンジル−L−グルタミン酸(10g、45.6mmol)を1,2−ジクロロエタン170mlに溶解させ、1−ドデカノール(10.2ml、45.6mmol、東京化成工業社製)ならびにp−トルエンスルホン酸1水和物(2.6g、13.68mmol)を加え、65℃で1日間攪拌を行い、γ−ベンジル−L−グルタミン酸/γ−ドデシル−L−グルタミン酸共重合体を得た。得られた共重合体について、下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)でエステル交換反応後の重合体の組成を測定した。
合成例4と同様の方法によりポリ−γ−ベンジル−L−グルタミン酸を得た後、1,2−ジクロロエタンに溶解させ、ポリ−γ−ベンジル−L−グルタミン酸のグルタミン酸単位に対して、当量のノルボルナン−2−メタノール(東京化成工業社製)と触媒量のp−トルエンスルホン酸1水和物を加え、65℃で4日間攪拌を行い、γ−ベンジル−L−グルタミン酸/γ−2−ノルボニルメチル−L−グルタミン酸共重合体を得た。得られた共重合体について、下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)でエステル交換反後の重合体の組成を測定した。
1,2−ジクロロエタン130mlにNα−カルボキシ−Nε−ベンジルオキシカルボニル−L−リジン無水物(4.02g、13.12mmol)ならびにN−カルボキシ−γ−メチル−L−グルタミン酸無水物(2.46g、13.12mmol)を入れ、開始剤としてN,N−ジメチル−1,3−プロパンジアミン(32.78μl、0.262mmol)を加え、25℃で1日間攪拌を行い、γ−メチル−L−グルタミン酸/Nε−ベンジルオキシカルボニル−L−リジン共重合体を得た。下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)で共重合体の組成を測定した。
合成例14と同様にして、1,2−ジクロロエタンに表2に示す2種のN−カルボキシ−L−アミノ酸無水物(成分A、成分B)を等モルずつ入れ、開始剤としてN,N−ジメチル−1,3−プロパンジアミンをアミノ酸無水物に対して1/100当量分加え、2~3日間攪拌を行い、各種ポリアミノ酸共重合体を得た。下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)で共重合体の組成を測定した。
1,2−ジクロロエタン20mlにN−カルボキシ−γ−メチル−L−グルタミン酸無水物(5.00g、26.72mmol)を入れた後、0℃まで冷却し、開始剤としてN,N−ジメチル−1,3−プロパンジアミン(66.80μl、0.534mmol)を加え、25℃で1日間攪拌を行った後、再び0℃まで冷却し、1,2−ジクロロエタン20mlを加えた後、Nα−カルボキシ−Nε−ベンジルオキシカルボニル−L−リジン無水物(4.09g、13.36mmol)を添加して、25℃で1日間攪拌を行い、γ−メチル−L−グルタミン酸−Nε−ベンジルオキシカルボニル−L−リジンブロック共重合体を得た。下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)で共重合体の組成を測定した。
合成例20と同様にして、γ−メチル−L−グルタミン酸−Nε−ベンジルオキシカルボニル−L−リジンブロック共重合体を得た後、再び0℃まで冷却し、1,2−ジクロロエタン10mlを加えた後、N−カルボキシ−γ−メチル−L−グルタミン酸無水物(5.00g、26.72mmol)を添加して、25℃で2日間攪拌を行い、γ−メチル−L−グルタミン酸−Nε−ベンジルオキシカルボニル−L−リジン−γ−メチル−L−グルタミン酸ブロック共重合体を得た。下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)で共重合体の組成を測定した。
1,2−ジクロロエタン10mlにN−カルボキシ−γ−ベンジル−L−グルタミン酸無水物(1.00g、3.80mmol)を入れた後、0℃まで冷却し、開始剤としてN,N−ジメチル−1,3−プロパンジアミン(9.56μl、0.076mmol)を加え、25℃で1日間攪拌を行った後、再び0℃まで冷却し、Nα−カルボキシ−Nε−ベンジルオキシカルボニル−L−リジン無水物(1.16g、3.80mmol)を添加して、25℃で1日間攪拌を行い、γ−ベンジル−L−グルタミン酸−Nε−ベンジルオキシカルボニル−L−リジンブロック共重合体(低分子量体)を得た。下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)で共重合体の組成を測定した。
1,2−ジクロロエタン10mlにNα−カルボキシ−Nε−ベンジルオキシカルボニル−L−リジン無水物(1.16g、3.80mmol)を入れた後、0℃まで冷却し、開始剤としてN,N−ジメチル−1,3−プロパンジアミン(9.56μl、0.076mmol)を加え、25℃で1日間攪拌を行った後、再び0℃まで冷却し、N−カルボキシ−γ−ベンジル−L−グルタミン酸無水物(1.00g、3.80mmol)を添加して、25℃で1日間攪拌を行い、γ−ベンジル−L−グルタミン酸−Nε−ベンジルオキシカルボニル−L−リジンブロック共重合体(低分子量体)を得た。下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)で共重合体の組成を測定した。
合成例22と同様の方法により、N−カルボキシ−γ−ベンジル−L−グルタミン酸無水物とNα−カルボキシ−Nε−ベンジルオキシカルボニル−L−リジン無水物を適量加えて、各種ポリα−アミノ酸ブロック共重合体(低分子量体)を得た。
1,2−ジクロロエタン10mlにN−カルボキシ−γ−ベンジル−L−グルタミン酸無水物(1.00g、3.80mmol)を入れた後、0℃まで冷却し、開始剤としてN,N−ジメチル−1,3−プロパンジアミン(0.48μl、3.8μmol)を加え、25℃で1日間攪拌を行った後、再び0℃まで冷却し、Nα−カルボキシ−Nε−ベンジルオキシカルボニル−L−リジン無水物(1.16g、3.80mmol)を添加して、25℃で3日間攪拌を行い、γ−ベンジル−L−グルタミン酸−Nε−ベンジルオキシカルボニル−L−リジンブロック共重合体(高分子量体)を得た。下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)で共重合体の組成を測定した。
(ステップ1)ポリ−γ−メチル−L−グルタミン酸(50%)−Nε−ベンジルオキシカルボニル−L−リジン(50%)ブロック共重合体の合成
合成例20と同様の方法にてポリ−γ−メチル−L−グルタミン酸(50%)−Nε−ベンジルオキシカルボニル−L−リジン(50%)ブロック共重合体を合成した。得られたブロック共重合体は下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)で共重合体の組成を測定した。
(ステップ2)ポリ−γ−メチル−L−グルタミン酸(50%)−Nε−ベンジルオキシカルボニル−L−リジン(50%)ブロック共重合体中のポリ−γ−メチル−L−グルタミン酸の側鎖置換反応(エステル交換反応)
上記で調製したポリ−γ−メチル−L−グルタミン酸(50%)−Nε−ベンジルオキシカルボニル−L−リジン(50%)ブロック共重合体5.47gを1,2−ジクロロエタン25mlに溶解させ、1−ヘキサノール(0.96ml、19.50mmol、東京化成工業社製)ならびにp−トルエンスルホン酸1水和物(0.075g、0.39mmol、東京化成工業社製)を加え、80℃で1日間攪拌してエステル交換反応を行い、γ−メチル−L−グルタミン酸/γ−ヘキシル−L−グルタミン酸共重合体を得た。得られた共重合体について、下記の方法(測定法1)で共重合体の重量平均分子量Mwを測定した。また、下記の方法(測定法2)でエステル交換反応後の重合体の組成を測定した。
1,2−ジクロロエタン10.7mlにN−カルボキシ−γ−メチル−L−グルタミン酸無水物(1.42g、7.60mmol)を入れた後、0℃まで冷却し、開始剤としてN,N−ジメチル−1,3−プロパンジアミン(0.96μl、7.6μmol)を加え、25℃で1日間攪拌を行った。
1,2−ジクロロエタン11.1mlにN−カルボキシ−γ−メチル−L−グルタミン酸無水物(2.00g、7.60mmol)を入れた後、0℃まで冷却し、開始剤としてN,N−ジメチル−1,3−プロパンジアミン(0.96μl、7.6μmol)を加え、25℃で1日間攪拌を行った。
合成例1、3、4、6、7、16、20、21、22、26のポリα−アミノ酸を使用し、以下の素子作製法に基づいて図1に示す素子を作製した。なお、ポリα−アミノ酸の薄膜(圧電体膜)の形成はキャスト法で行った。
(素子作製法)
電極2としてITO(酸化インジウムスズ)電極を蒸着したポリエチレンテレフタレート(PET)基板1(厚み:125±5μm)をメタノールで洗浄した。洗浄した基板(縦:18mm、横:12mm)上に、圧電体膜3として、ポリα—アミノ酸溶液からキャスト法でポリマー薄膜を作製した。この薄膜を、ITO電極を蒸着したPET基板4で挟み込むことで素子を作製した。
測定法1:重量平均分子量の測定方法
重量平均分子量Mwはゲル浸透クロマトグラフィー(GPC)を用いて測定した。具体的には、分析カラム装置(昭和電工社製、Shodex K−802ならびにK−806M)をGPC用分析装置(日立社製、LaChrom Elite)に取り付け、別途調製した測定溶液を10~80μl注入し、溶離液流速:1ml/分、カラム保持温度:40℃、溶媒:クロロホルムの条件にて測定を行った。測定溶液は、ポリアミノ酸濃度が0.25~3.0%(w/v)となるようにクロロホルムに溶解させた後、フィルター濾過を行うことで調製した。得られたピークの保持時間と別途測定した較正用ポリスチレン(昭和電工社製、Shodex STANDARD SM−105)のピークの保持時間を比較することで、重量平均分子量Mwを算出した。
サンプル十数mgを重クロロホルムもしくは重トリフルオロ酢酸に溶解した後、1H核磁気共鳴スペクトル(1HNMR、BRUKER社、400MHz)を分析し、エステル交換前後もしくは共重合時のアミノ酸のα位のプロトンのピーク面積を比較することで、組成を算出した。測定例を以下に示す。
合成した共重合体10mgを重トリフルオロ酢酸に溶解し、1HNMRを測定したところ、3.8ppm付近にγ−メチル−L−グルタミン酸のメチル基由来ピークが、また4.7ppm付近にγ−メチル−L−グルタミン酸およびγ−ヘキシル−L−グルタミン酸のα位のプロトンに由来するピークが検出された。3.8ppm付近のピーク面積をA、4.7ppm付近のピーク面積をBとするとA/B=1.17であった。ポリ−γ−メチル−L−グルタミン酸の場合は、A/B=3.00であることから、減少分だけヘキシル基に置換していると考えられる。従って、ヘキシル基の含有率は、1.83/3.00=0.61から61%となる。故に共重合体の組成は、γ−メチル−L−グルタミン酸(39%)/γ−ヘキシル−L−グルタミン酸(61%)となる。
合成した共重合体10mgを重トリフルオロ酢酸に溶解し、1HNMRを測定したところ、5.1ppm付近にNε−ベンジルオキシカルボニル−L−リジンのベンジル基およびγ−ベンジル−L−グルタミン酸のベンジル基由来ピークが、また4.7ppm付近にγ−ベンジル−L−グルタミン酸、4.4ppm付近にNε−ベンジルオキシカルボニル−L−リジンのα位のプロトンに由来するピークが検出された。5.1ppm、4.7ppm、4.4ppm付近のピーク面積をそれぞれA、B、CとするとA/B=4.00、A/C=4.00、B/C=1.00であった。B、Cはともにプロトン1個分の面積を表しているので、共重合体の組成はγ−ベンジル−L−グルタミン酸(50%)/Nε−ベンジルオキシカルボニル−L−リジン(50%)となる。
合成した各種ポリアミノ酸溶液を銅箔(JX 日鉱日石金属株式会社製 JTC 35μm)に塗布した後室温にて12時間以上放置し、乾燥させた。これを1cm角に裁断、d33メーター(株式会社日本フェロテクノロジー製 NPT22001T)を用いて圧電定数d33の値を測定した。この時、上部接触電極5φ、荷重150gにて測定を行った。
作製した素子に負荷(約6kg)をかけた際に発現する起電力を、KEITHLEY社製のソースメータを用いて室温(20℃)で測定し、膜厚から電界の大きさを求めることで圧電素子を評価した。評価基準は以下の通りである。
◎:電界が0.50V/μm以上
○:電界が0.30V/μm以上、0.50V/μm未満
△:電界が0.25V/μm以上、0.30V/μm未満
×:電界が0.25V/μm未満
各種溶媒80重量部に、合成した化合物20重量部を加え溶液となった場合に20w%となる比率で混合し、室温で攪拌し、溶解性を評価した。
評価基準は以下の通りである。
○:完全に溶解
△:一部可溶
×:不溶
ジクロロメタン:純正化学社製、特級
シクロヘキサノン:東京化成工業社製
N,N−ジメチルアセトアミド:関東化学社製、鹿特級
安息香酸メチル:関東化学社製、鹿特級
トルエン:純正化学社製、特級
トリグライム(トリエチレングリコールジメチルエーテル):ナカライテスク社製
2 下部電極
3 圧電体膜(ポリα−アミノ酸)
4 上部電極
5 フレキシブル基板
6 ソースメータ
7 圧力印加機械
Claims (15)
- (A)式(I)で表されるグルタミン酸γ−エステル単位:
式(I):
(式中、R1はメチル基またはベンジル基を表す。)と、
(B)式(II)で表されるグルタミン酸γ−エステル単位、式(III)で表されるアラニン単位、フェニルアラニン単位およびNε−ベンジルオキシカルボニルリジン単位、ならびに式(IV)で表されるグルタミン酸γ−エステル単位から選択される1種以上の単位:
式(II):
(式中、R2は炭素数が6~18の非置換のアルキル基、または、水素原子の一部もしくは全部が、ハロゲン原子もしくは炭素数が3~12の脂環式炭化水素基で置換された炭素数が1~6の置換アルキル基を表す。)
式(III):
(式中、R3はメチル基、ベンジル基または(CH2)4−NHZ基(基中、Zはベンジルオキシカルボニル基を表す。)を表す。)
式(IV):
(式中、R4は炭素数が1~12のアルコキシ基、水素原子の一部もしくは全部がハロゲン原子で置換された炭素数が1~12のアルキル基、または、アルキル基の炭素数が1~12のアルキルカルボニル基を表し、m個のR4は同一でも異なってもよい。lは6~12の整数、mは1~3の整数を表す。)
を含有するポリα−アミノ酸を含む圧電素子。 - R2が炭素数6~18の非置換のアルキル基、または、水素原子の一部もしくは全部がフッ素原子もしくはノルボルニル基で置換された炭素数が1~6の置換アルキル基である請求項1記載の圧電素子。
- R2がn−ヘキシル基、n−ドデシル基、n−ヘキサデシル基、2−ノルボニルメチル基または2,2,2−トリフルオロエチル基である請求項1または2に記載の圧電素子。
- R3が(CH2)4−NHZ基(基中、Zはベンジルオキシカルボニル基を表す)である請求項1から3のいずれか一項に記載の圧電素子。
- R4が炭素数が1~6のアルコキシ基、水素原子の一部もしくは全部がフッ素原子で置換された炭素数が1~12のアルキル基、または、アルキル基の炭素数が3~9のアルキルカルボニル基である請求項1から4のいずれか一項に記載の圧電素子。
- R4がメトキシ基、ブトキシ基、ヘキシルオキシ基、トリフルオロメチル基、またはn−ヘキシルカルボニル基である請求項1から5のいずれか一項に記載の圧電素子。
- ポリアミノ酸が、γ−メチル−L−グルタミン酸/γ−ヘキシル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−ドデシル−L−グルタミン酸共重合体、γ−ベンジル−L−グルタミン酸/γ−ドデシル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−ヘキサデシル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−2,2,2−トリフルオロエチル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−2−ノルボルニルメチル−L−グルタミン酸共重合体、γ−ベンジル−L−グルタミン酸/γ−2−ノルボルニルメチル−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(6−(p−メトキシフェノキシ)−1−ヘキシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(6−(p−ヘキシルカルボニルフェノキシ)−1−ヘキシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(10−(p−メトキシフェノキシ)−1−デシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(6−(p−ブトキシフェノキシ)−1−ヘキシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(6−(p−ヘキシルオキシフェノキシ)−1−ヘキシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/γ−(6−(3,5−ビス(トリフルオロメチル)フェノキシ)−1−ヘキシル)−L−グルタミン酸共重合体、γ−メチル−L−グルタミン酸/Nε−ベンジルオキシカルボニル−L−リジン共重合体、γ−ベンジル−L−グルタミン酸/Nε−ベンジルオキシカルボニル−L−リジン共重合体、γ−メチル−L−グルタミン酸/L−フェニルアラニン共重合体、γ−ベンジル−L−グルタミン酸/L−フェニルアラニン共重合体、およびγ−ベンジル−L−グルタミン酸/L−アラニン共重合体から選択される1種以上である請求項1記載の圧電素子。
- ポリα−アミノ酸がランダム共重合体である請求項1から7のいずれか一項に記載の圧電素子。
- ポリα−アミノ酸がブロック共重合体である請求項1から7のいずれか一項に記載の圧電素子。
- ポリα−アミノ酸の重量平均分子量(Mw)が1,000~5,000,000であることを特徴とする請求項1から9のいずれか一項に記載の圧電素子。
- フレキシブル基板、電極、およびポリα−アミノ酸を有することを特徴とする請求項1から10のいずれか一項に記載の圧電素子。
- ポリα−アミノ酸が薄膜状であることを特徴とする請求項1から11のいずれか一項に記載の圧電素子。
- ポリα−アミノ酸の薄膜が500nm~500μmの薄膜状であることを特徴とする請求項12記載の圧電素子。
- フレキシブル基板上に、下部電極、ポリα−アミノ酸、上部電極を積層させることを特徴とする請求項1から13のいずれか一項に記載の圧電素子を製造する方法。
- 請求項1から13のいずれか一項に記載の圧電素子を製造するための、ポリアミノ酸含有インク。
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201380009404.0A CN104247066A (zh) | 2012-02-14 | 2013-02-13 | 压电元件 |
EP13748687.4A EP2816623A4 (en) | 2012-02-14 | 2013-02-13 | PIEZOELECTRIC ELEMENT |
JP2013558769A JP6007921B2 (ja) | 2012-02-14 | 2013-02-13 | 圧電素子 |
KR1020147025519A KR20140129160A (ko) | 2012-02-14 | 2013-02-13 | 압전 소자 |
US14/458,632 US9450174B2 (en) | 2012-02-14 | 2014-08-13 | Piezoelectric element |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012029031 | 2012-02-14 | ||
JP2012-029031 | 2012-02-14 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/458,632 Continuation US9450174B2 (en) | 2012-02-14 | 2014-08-13 | Piezoelectric element |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2013122257A1 true WO2013122257A1 (ja) | 2013-08-22 |
Family
ID=48984364
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2013/054240 WO2013122257A1 (ja) | 2012-02-14 | 2013-02-13 | 圧電素子 |
Country Status (7)
Country | Link |
---|---|
US (1) | US9450174B2 (ja) |
EP (1) | EP2816623A4 (ja) |
JP (1) | JP6007921B2 (ja) |
KR (1) | KR20140129160A (ja) |
CN (1) | CN104247066A (ja) |
TW (1) | TW201402652A (ja) |
WO (1) | WO2013122257A1 (ja) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6112010B2 (ja) * | 2011-05-12 | 2017-04-12 | 味の素株式会社 | ポリα−アミノ酸およびそれを用いた強誘電体メモリ素子 |
US10190854B2 (en) * | 2015-06-22 | 2019-01-29 | Smart Target Systems Llc | Shooting target system |
JP6447779B2 (ja) * | 2016-04-22 | 2019-01-09 | 株式会社村田製作所 | モニタリングシステム |
US20220231218A1 (en) * | 2021-01-21 | 2022-07-21 | Wisconsin Alumni Research Foundation | Wafer-Scale Piezoelectric Bio-Organic Thin Films |
KR102595641B1 (ko) * | 2021-08-09 | 2023-10-30 | 전북대학교산학협력단 | 압전 소자의 프린팅용 조성물, 이의 제조 방법 및 이를 이용한 압전 소자용 프린터 |
KR102671906B1 (ko) * | 2023-03-07 | 2024-06-05 | 재단법인 구미전자정보기술원 | 힘센서 기반 생체정보 측정 웨어러블 스마트 밴드 및 이를 이용한 생체정보 제공 시스템 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63128317A (ja) * | 1986-11-19 | 1988-05-31 | Rikagaku Kenkyusho | コレステリツク液晶性ポリマ−の選択反射波長可変方法 |
JPH03156430A (ja) * | 1989-11-14 | 1991-07-04 | Rikagaku Kenkyusho | 非線形光学材料 |
JPH04102827A (ja) * | 1990-08-22 | 1992-04-03 | Nippon Oil Co Ltd | ポリペプチドの配向方法 |
JPH0824625A (ja) * | 1994-07-19 | 1996-01-30 | Kyowa Hakko Kogyo Co Ltd | ポリグルタミン酸γ−エステル含有マイクロカプセル及びその固定化方法 |
JPH11217432A (ja) | 1998-02-04 | 1999-08-10 | Nippon Mitsubishi Oil Corp | 強誘電性液晶ポリマーおよびその用途 |
JP2005217111A (ja) | 2004-01-29 | 2005-08-11 | Sumitomo Heavy Ind Ltd | 高分子圧電体及びそれを製造する装置 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPWO2006062207A1 (ja) * | 2004-12-10 | 2008-06-12 | 三井化学株式会社 | アミノ酸重合体組成物およびその用途 |
JP6112010B2 (ja) * | 2011-05-12 | 2017-04-12 | 味の素株式会社 | ポリα−アミノ酸およびそれを用いた強誘電体メモリ素子 |
-
2013
- 2013-02-08 TW TW102105611A patent/TW201402652A/zh unknown
- 2013-02-13 CN CN201380009404.0A patent/CN104247066A/zh active Pending
- 2013-02-13 EP EP13748687.4A patent/EP2816623A4/en not_active Withdrawn
- 2013-02-13 WO PCT/JP2013/054240 patent/WO2013122257A1/ja active Application Filing
- 2013-02-13 KR KR1020147025519A patent/KR20140129160A/ko not_active Application Discontinuation
- 2013-02-13 JP JP2013558769A patent/JP6007921B2/ja active Active
-
2014
- 2014-08-13 US US14/458,632 patent/US9450174B2/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63128317A (ja) * | 1986-11-19 | 1988-05-31 | Rikagaku Kenkyusho | コレステリツク液晶性ポリマ−の選択反射波長可変方法 |
JPH03156430A (ja) * | 1989-11-14 | 1991-07-04 | Rikagaku Kenkyusho | 非線形光学材料 |
JPH04102827A (ja) * | 1990-08-22 | 1992-04-03 | Nippon Oil Co Ltd | ポリペプチドの配向方法 |
JPH0824625A (ja) * | 1994-07-19 | 1996-01-30 | Kyowa Hakko Kogyo Co Ltd | ポリグルタミン酸γ−エステル含有マイクロカプセル及びその固定化方法 |
JPH11217432A (ja) | 1998-02-04 | 1999-08-10 | Nippon Mitsubishi Oil Corp | 強誘電性液晶ポリマーおよびその用途 |
JP2005217111A (ja) | 2004-01-29 | 2005-08-11 | Sumitomo Heavy Ind Ltd | 高分子圧電体及びそれを製造する装置 |
Non-Patent Citations (1)
Title |
---|
See also references of EP2816623A4 |
Also Published As
Publication number | Publication date |
---|---|
US20140368083A1 (en) | 2014-12-18 |
JP6007921B2 (ja) | 2016-10-19 |
EP2816623A4 (en) | 2015-11-04 |
JPWO2013122257A1 (ja) | 2015-05-21 |
CN104247066A (zh) | 2014-12-24 |
KR20140129160A (ko) | 2014-11-06 |
US9450174B2 (en) | 2016-09-20 |
TW201402652A (zh) | 2014-01-16 |
EP2816623A1 (en) | 2014-12-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6007921B2 (ja) | 圧電素子 | |
WO2014073628A1 (ja) | メンブレンスイッチおよびそれを用いてなる物品 | |
KR101514861B1 (ko) | 액정 배향 처리제, 및 그것을 사용한 액정 표시 소자 | |
KR101589322B1 (ko) | 액정 배향제, 액정 배향막 및 액정 표시 소자 | |
TWI477478B (zh) | Diamine compounds, polyamic acid, polyimide and liquid crystal alignment treatment agent | |
CN103739523B (zh) | 液晶取向处理剂 | |
JP5663876B2 (ja) | 液晶配向処理剤、及びそれを用いた液晶表示素子 | |
JP2011529509A (ja) | ポリイソシアネートを基礎とするポリマー素子を有する電気機械変換器 | |
US9464167B2 (en) | Poly α-amino acid and ferroelectric memory element using same | |
JP5633369B2 (ja) | 有機圧電材料、それを用いた超音波振動子、その製造方法、超音波探触子及び超音波医用画像診断装置 | |
JP5098790B2 (ja) | 有機圧電膜、それを用いた超音波振動子、その製造方法、超音波探触子及び超音波医用画像診断装置 | |
US20240294794A1 (en) | Copolymer, piezoelectric material, piezoelectric film and piezoelectric element | |
JPWO2009025145A1 (ja) | 有機圧電体膜、その形成方法、それを用いた超音波振動子、超音波探触子、及び超音波医用画像診断装置 | |
JP2009224954A (ja) | 有機圧電材料、それを用いた超音波振動子、その製造方法、超音波探触子及び超音波医用画像診断装置 | |
TW200420982A (en) | Liquid crystal alignment layer forming method | |
JP5310555B2 (ja) | 有機圧電体 | |
JP2011224980A (ja) | 向上した接着性を有するポリマー積層複合材料 | |
Kwangmok et al. | Poly (vinylidene fluoride) piezoelectric film characteristics by poling conditions for distributed tactile sensor | |
Fukada et al. | Polyureas and polythioureas | |
Wang et al. | Low-temperature piezoelectric and dielectric properties of aromatic polyureas prepared by vapour deposition polymerization | |
CN114830024A (zh) | 液晶取向膜、自由基产生膜、以及水平电场液晶单元的制造方法 | |
CN116997854A (zh) | 液晶组合物、液晶显示元件的制造方法及液晶显示元件 | |
Hamciuc et al. | Modified aromatic polyimides with potential piezoelectric properties | |
Murata et al. | Ferroelectric behavior and hydrogen bonding in polyamides |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 13748687 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2013558769 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
REEP | Request for entry into the european phase |
Ref document number: 2013748687 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2013748687 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 20147025519 Country of ref document: KR Kind code of ref document: A |