JP5682062B2 - 硬化性組成物 - Google Patents
硬化性組成物 Download PDFInfo
- Publication number
- JP5682062B2 JP5682062B2 JP2010535845A JP2010535845A JP5682062B2 JP 5682062 B2 JP5682062 B2 JP 5682062B2 JP 2010535845 A JP2010535845 A JP 2010535845A JP 2010535845 A JP2010535845 A JP 2010535845A JP 5682062 B2 JP5682062 B2 JP 5682062B2
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- Prior art keywords
- compound
- thiol
- alkenyl
- molecule
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000203 mixture Substances 0.000 title claims description 60
- -1 thiol compound Chemical class 0.000 claims description 159
- 150000001875 compounds Chemical class 0.000 claims description 91
- 125000003342 alkenyl group Chemical group 0.000 claims description 52
- 125000004434 sulfur atom Chemical group 0.000 claims description 30
- 229910052717 sulfur Inorganic materials 0.000 claims description 29
- 125000004432 carbon atom Chemical group C* 0.000 claims description 26
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 25
- 150000002894 organic compounds Chemical class 0.000 claims description 24
- 239000004641 Diallyl-phthalate Substances 0.000 claims description 21
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 21
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 claims description 21
- 229910052799 carbon Inorganic materials 0.000 claims description 21
- 229910052710 silicon Inorganic materials 0.000 claims description 20
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 18
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 14
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 13
- 238000007259 addition reaction Methods 0.000 claims description 12
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 claims description 12
- 239000010936 titanium Substances 0.000 claims description 11
- ARCGXLSVLAOJQL-UHFFFAOYSA-N anhydrous trimellitic acid Natural products OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 claims description 10
- 239000000243 solution Substances 0.000 claims description 9
- 229910052719 titanium Inorganic materials 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- JRNVQLOKVMWBFR-UHFFFAOYSA-N 1,2-benzenedithiol Chemical compound SC1=CC=CC=C1S JRNVQLOKVMWBFR-UHFFFAOYSA-N 0.000 claims description 8
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 8
- 238000006459 hydrosilylation reaction Methods 0.000 claims description 8
- MXTOXODEXBYZFX-UHFFFAOYSA-N 2-[2-(2-sulfanylethylsulfanyl)ethylsulfanyl]ethanethiol Chemical compound SCCSCCSCCS MXTOXODEXBYZFX-UHFFFAOYSA-N 0.000 claims description 7
- 238000009833 condensation Methods 0.000 claims description 7
- 230000005494 condensation Effects 0.000 claims description 7
- 230000003301 hydrolyzing effect Effects 0.000 claims description 7
- 150000003573 thiols Chemical class 0.000 claims description 7
- 125000006574 non-aromatic ring group Chemical group 0.000 claims description 6
- ROLAGNYPWIVYTG-UHFFFAOYSA-N 1,2-bis(4-methoxyphenyl)ethanamine;hydrochloride Chemical compound Cl.C1=CC(OC)=CC=C1CC(N)C1=CC=C(OC)C=C1 ROLAGNYPWIVYTG-UHFFFAOYSA-N 0.000 claims description 4
- NNJWFWSBENPGEY-UHFFFAOYSA-N [2-(sulfanylmethyl)phenyl]methanethiol Chemical compound SCC1=CC=CC=C1CS NNJWFWSBENPGEY-UHFFFAOYSA-N 0.000 claims description 4
- JOBBTVPTPXRUBP-UHFFFAOYSA-N [3-(3-sulfanylpropanoyloxy)-2,2-bis(3-sulfanylpropanoyloxymethyl)propyl] 3-sulfanylpropanoate Chemical compound SCCC(=O)OCC(COC(=O)CCS)(COC(=O)CCS)COC(=O)CCS JOBBTVPTPXRUBP-UHFFFAOYSA-N 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- PPQNMKIMOCEJIR-UHFFFAOYSA-N benzene-1,2,3-trithiol Chemical compound SC1=CC=CC(S)=C1S PPQNMKIMOCEJIR-UHFFFAOYSA-N 0.000 claims description 4
- JRMHUZLFQVKRNB-UHFFFAOYSA-N bis(ethenyl)-diphenylsilane Chemical compound C=1C=CC=CC=1[Si](C=C)(C=C)C1=CC=CC=C1 JRMHUZLFQVKRNB-UHFFFAOYSA-N 0.000 claims description 4
- ZDNFTNPFYCKVTB-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,4-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C=C1 ZDNFTNPFYCKVTB-UHFFFAOYSA-N 0.000 claims description 4
- ZODWTWYKYYGSFS-UHFFFAOYSA-N diphenyl-bis(prop-2-enyl)silane Chemical compound C=1C=CC=CC=1[Si](CC=C)(CC=C)C1=CC=CC=C1 ZODWTWYKYYGSFS-UHFFFAOYSA-N 0.000 claims description 4
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 3
- GZWLFCGQNCRLIN-UHFFFAOYSA-N 1,2-bis(prop-2-enoxy)benzene Chemical compound C=CCOC1=CC=CC=C1OCC=C GZWLFCGQNCRLIN-UHFFFAOYSA-N 0.000 claims description 3
- SCZZNWQQCGSWSZ-UHFFFAOYSA-N 1-prop-2-enoxy-4-[2-(4-prop-2-enoxyphenyl)propan-2-yl]benzene Chemical compound C=1C=C(OCC=C)C=CC=1C(C)(C)C1=CC=C(OCC=C)C=C1 SCZZNWQQCGSWSZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
- WYLSFPGWSGKZFL-UHFFFAOYSA-N C1SSC=C1.C1=CC=CC2=CC=CC=C21 Chemical compound C1SSC=C1.C1=CC=CC2=CC=CC=C21 WYLSFPGWSGKZFL-UHFFFAOYSA-N 0.000 claims description 3
- DSQPRECRRGZSCV-UHFFFAOYSA-N penta-1,4-dien-3-yl(phenyl)silane Chemical compound C=CC([SiH2]c1ccccc1)C=C DSQPRECRRGZSCV-UHFFFAOYSA-N 0.000 claims description 3
- DBSDMAPJGHBWAL-UHFFFAOYSA-N penta-1,4-dien-3-ylbenzene Chemical compound C=CC(C=C)C1=CC=CC=C1 DBSDMAPJGHBWAL-UHFFFAOYSA-N 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- IMQFZQVZKBIPCQ-UHFFFAOYSA-N 2,2-bis(3-sulfanylpropanoyloxymethyl)butyl 3-sulfanylpropanoate Chemical compound SCCC(=O)OCC(CC)(COC(=O)CCS)COC(=O)CCS IMQFZQVZKBIPCQ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001721 carbon Chemical group 0.000 claims 2
- WVAFEFUPWRPQSY-UHFFFAOYSA-N 1,2,3-tris(ethenyl)benzene Chemical compound C=CC1=CC=CC(C=C)=C1C=C WVAFEFUPWRPQSY-UHFFFAOYSA-N 0.000 claims 1
- PWLMPCKUIUTQFV-UHFFFAOYSA-N 2-methylprop-1-enyl-[2-(2-methylprop-1-enylsilyl)phenyl]silane Chemical compound CC(=C[SiH2]C1=C(C=CC=C1)[SiH2]C=C(C)C)C PWLMPCKUIUTQFV-UHFFFAOYSA-N 0.000 claims 1
- 239000000376 reactant Substances 0.000 description 25
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- JLLMOYPIVVKFHY-UHFFFAOYSA-N Benzenethiol, 4,4'-thiobis- Chemical compound C1=CC(S)=CC=C1SC1=CC=C(S)C=C1 JLLMOYPIVVKFHY-UHFFFAOYSA-N 0.000 description 15
- 239000000047 product Substances 0.000 description 14
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 13
- 239000007795 chemical reaction product Substances 0.000 description 13
- 239000007788 liquid Substances 0.000 description 13
- 239000000758 substrate Substances 0.000 description 13
- JZQAAQZDDMEFGZ-UHFFFAOYSA-N bis(ethenyl) hexanedioate Chemical compound C=COC(=O)CCCCC(=O)OC=C JZQAAQZDDMEFGZ-UHFFFAOYSA-N 0.000 description 12
- 239000011521 glass Substances 0.000 description 12
- 238000002156 mixing Methods 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- 239000010408 film Substances 0.000 description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 9
- 239000010409 thin film Substances 0.000 description 9
- UHXCHUWSQRLZJS-UHFFFAOYSA-N (4-dimethylsilylidenecyclohexa-2,5-dien-1-ylidene)-dimethylsilane Chemical compound C[Si](C)C1=CC=C([Si](C)C)C=C1 UHXCHUWSQRLZJS-UHFFFAOYSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 8
- VJHGSLHHMIELQD-UHFFFAOYSA-N nona-1,8-diene Chemical compound C=CCCCCCC=C VJHGSLHHMIELQD-UHFFFAOYSA-N 0.000 description 8
- XVSSGIXTKVRGAR-UHFFFAOYSA-N prop-2-enoxycarbonyl prop-2-enyl carbonate Chemical compound C=CCOC(=O)OC(=O)OCC=C XVSSGIXTKVRGAR-UHFFFAOYSA-N 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 6
- 125000004429 atom Chemical group 0.000 description 6
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Substances SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 6
- XWJBRBSPAODJER-UHFFFAOYSA-N 1,7-octadiene Chemical compound C=CCCCCC=C XWJBRBSPAODJER-UHFFFAOYSA-N 0.000 description 4
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- YCLSOMLVSHPPFV-UHFFFAOYSA-N 3-(2-carboxyethyldisulfanyl)propanoic acid Chemical compound OC(=O)CCSSCCC(O)=O YCLSOMLVSHPPFV-UHFFFAOYSA-N 0.000 description 4
- 239000007983 Tris buffer Substances 0.000 description 4
- IYPNRTQAOXLCQW-UHFFFAOYSA-N [4-(sulfanylmethyl)phenyl]methanethiol Chemical compound SCC1=CC=C(CS)C=C1 IYPNRTQAOXLCQW-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- VDCSGNNYCFPWFK-UHFFFAOYSA-N diphenylsilane Chemical compound C=1C=CC=CC=1[SiH2]C1=CC=CC=C1 VDCSGNNYCFPWFK-UHFFFAOYSA-N 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 230000008646 thermal stress Effects 0.000 description 4
- PQVDTVNAMGYHDQ-UHFFFAOYSA-N 1,2-bis(prop-2-enyl)benzene Chemical compound C=CCC1=CC=CC=C1CC=C PQVDTVNAMGYHDQ-UHFFFAOYSA-N 0.000 description 3
- WEERVPDNCOGWJF-UHFFFAOYSA-N 1,4-bis(ethenyl)benzene Chemical compound C=CC1=CC=C(C=C)C=C1 WEERVPDNCOGWJF-UHFFFAOYSA-N 0.000 description 3
- JVTMVUFBBYUSKS-UHFFFAOYSA-N 1,4-bis(prop-2-enyl)benzene Chemical compound C=CCC1=CC=C(CC=C)C=C1 JVTMVUFBBYUSKS-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000006087 Silane Coupling Agent Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- WYLQRHZSKIDFEP-UHFFFAOYSA-N benzene-1,4-dithiol Chemical compound SC1=CC=C(S)C=C1 WYLQRHZSKIDFEP-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 3
- 239000004611 light stabiliser Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- AAPAGLBSROJFGM-UHFFFAOYSA-N naphthalene-1,5-dithiol Chemical compound C1=CC=C2C(S)=CC=CC2=C1S AAPAGLBSROJFGM-UHFFFAOYSA-N 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- CLNYHERYALISIR-FNORWQNLSA-N (3e)-nona-1,3-diene Chemical compound CCCCC\C=C\C=C CLNYHERYALISIR-FNORWQNLSA-N 0.000 description 2
- ARKHCBWJALMQJO-UHFFFAOYSA-N 1,2-bis(ethenyl)cyclohexane Chemical compound C=CC1CCCCC1C=C ARKHCBWJALMQJO-UHFFFAOYSA-N 0.000 description 2
- SYENRPHLJLKTED-UHFFFAOYSA-N 1,3,5-tris(ethenyl)benzene Chemical compound C=CC1=CC(C=C)=CC(C=C)=C1 SYENRPHLJLKTED-UHFFFAOYSA-N 0.000 description 2
- AANPQJBOJRZUNO-UHFFFAOYSA-N 1,4-bis(prop-2-enoxy)benzene Chemical compound C=CCOC1=CC=C(OCC=C)C=C1 AANPQJBOJRZUNO-UHFFFAOYSA-N 0.000 description 2
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 2
- MTZVWTOVHGKLOX-UHFFFAOYSA-N 2,2-bis(sulfanylmethyl)propane-1,3-dithiol Chemical compound SCC(CS)(CS)CS MTZVWTOVHGKLOX-UHFFFAOYSA-N 0.000 description 2
- WFUMVIYEGASPLY-UHFFFAOYSA-N 2-[2,3,4-tris(2-sulfanylethyl)phenyl]ethanethiol Chemical compound SCCC1=CC=C(CCS)C(CCS)=C1CCS WFUMVIYEGASPLY-UHFFFAOYSA-N 0.000 description 2
- ODJQKYXPKWQWNK-UHFFFAOYSA-N 3,3'-Thiobispropanoic acid Chemical compound OC(=O)CCSCCC(O)=O ODJQKYXPKWQWNK-UHFFFAOYSA-N 0.000 description 2
- CARNFEUGBMWTON-UHFFFAOYSA-N 3-(2-prop-2-enoxyethoxy)prop-1-ene Chemical compound C=CCOCCOCC=C CARNFEUGBMWTON-UHFFFAOYSA-N 0.000 description 2
- XSSOJMFOKGTAFU-UHFFFAOYSA-N 3-[2-(2-prop-2-enoxyethoxy)ethoxy]prop-1-ene Chemical compound C=CCOCCOCCOCC=C XSSOJMFOKGTAFU-UHFFFAOYSA-N 0.000 description 2
- DKIDEFUBRARXTE-UHFFFAOYSA-M 3-mercaptopropionate Chemical compound [O-]C(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-M 0.000 description 2
- FYRWKWGEFZTOQI-UHFFFAOYSA-N 3-prop-2-enoxy-2,2-bis(prop-2-enoxymethyl)propan-1-ol Chemical compound C=CCOCC(CO)(COCC=C)COCC=C FYRWKWGEFZTOQI-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000003490 Thiodipropionic acid Substances 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- COYTVZAYDAIHDK-UHFFFAOYSA-N [5-(sulfanylmethyl)-1,4-dithian-2-yl]methanethiol Chemical compound SCC1CSC(CS)CS1 COYTVZAYDAIHDK-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- JQRRFDWXQOQICD-UHFFFAOYSA-N biphenylen-1-ylboronic acid Chemical compound C12=CC=CC=C2C2=C1C=CC=C2B(O)O JQRRFDWXQOQICD-UHFFFAOYSA-N 0.000 description 2
- HABAXTXIECRCKH-UHFFFAOYSA-N bis(prop-2-enyl) butanedioate Chemical compound C=CCOC(=O)CCC(=O)OCC=C HABAXTXIECRCKH-UHFFFAOYSA-N 0.000 description 2
- JKJWYKGYGWOAHT-UHFFFAOYSA-N bis(prop-2-enyl) carbonate Chemical compound C=CCOC(=O)OCC=C JKJWYKGYGWOAHT-UHFFFAOYSA-N 0.000 description 2
- FPODCVUTIPDRTE-UHFFFAOYSA-N bis(prop-2-enyl) hexanedioate Chemical compound C=CCOC(=O)CCCCC(=O)OCC=C FPODCVUTIPDRTE-UHFFFAOYSA-N 0.000 description 2
- BKXRKRANFLFTFU-UHFFFAOYSA-N bis(prop-2-enyl) oxalate Chemical compound C=CCOC(=O)C(=O)OCC=C BKXRKRANFLFTFU-UHFFFAOYSA-N 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- NLDGJRWPPOSWLC-UHFFFAOYSA-N deca-1,9-diene Chemical compound C=CCCCCCCC=C NLDGJRWPPOSWLC-UHFFFAOYSA-N 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- VLNRSEGRGSDKLS-UHFFFAOYSA-N ethenyl-[4-[ethenyl(dimethyl)silyl]phenyl]-dimethylsilane Chemical compound C=C[Si](C)(C)C1=CC=C([Si](C)(C)C=C)C=C1 VLNRSEGRGSDKLS-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
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- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- HYRAFPWOUAMMQN-UHFFFAOYSA-N naphthalene-1,4-dithiol Chemical compound C1=CC=C2C(S)=CC=C(S)C2=C1 HYRAFPWOUAMMQN-UHFFFAOYSA-N 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 235000019303 thiodipropionic acid Nutrition 0.000 description 2
- 239000012780 transparent material Substances 0.000 description 2
- 229960000834 vinyl ether Drugs 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- CAYNCHQZXZMUEX-UHFFFAOYSA-N (hydroxymethyldisulfanyl)methanol 2-sulfanylacetic acid Chemical compound OC(=O)CS.OC(=O)CS.OCSSCO CAYNCHQZXZMUEX-UHFFFAOYSA-N 0.000 description 1
- BXGKVFOHNHSLHH-UHFFFAOYSA-N (hydroxymethyldisulfanyl)methanol 3-sulfanylpropanoic acid Chemical compound OCSSCO.OC(=O)CCS.OC(=O)CCS BXGKVFOHNHSLHH-UHFFFAOYSA-N 0.000 description 1
- RHMKQRWOFRAOHS-UHFFFAOYSA-N (sulfanylmethyldisulfanyl)methanethiol Chemical compound SCSSCS RHMKQRWOFRAOHS-UHFFFAOYSA-N 0.000 description 1
- VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 description 1
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- QULSCWWJJFURRB-UHFFFAOYSA-N [10-(sulfanylmethyl)anthracen-9-yl]methanethiol Chemical compound C1=CC=C2C(CS)=C(C=CC=C3)C3=C(CS)C2=C1 QULSCWWJJFURRB-UHFFFAOYSA-N 0.000 description 1
- FNTKCWQKAGGZFV-UHFFFAOYSA-N [2,3,4-tris(sulfanylmethyl)phenyl]methanethiol Chemical compound SCC1=CC=C(CS)C(CS)=C1CS FNTKCWQKAGGZFV-UHFFFAOYSA-N 0.000 description 1
- SDEFSQDZLUZWPW-UHFFFAOYSA-N [2,3-bis(sulfanylmethyl)phenyl]methanethiol Chemical compound SCC1=CC=CC(CS)=C1CS SDEFSQDZLUZWPW-UHFFFAOYSA-N 0.000 description 1
- IQQCGSKMZYRXLC-UHFFFAOYSA-N [2,3-bis(sulfanylmethylsulfanyl)phenyl]sulfanylmethanethiol Chemical compound SCSC1=CC=CC(SCS)=C1SCS IQQCGSKMZYRXLC-UHFFFAOYSA-N 0.000 description 1
- BVEGHZVZLLPALO-UHFFFAOYSA-N [2,4,5-tris(sulfanylmethoxy)phenoxy]methanethiol Chemical compound SCOC1=CC(OCS)=C(OCS)C=C1OCS BVEGHZVZLLPALO-UHFFFAOYSA-N 0.000 description 1
- LJODQQVXMSKBHT-UHFFFAOYSA-N [2,4,5-tris(sulfanylmethyl)phenyl]methanethiol Chemical compound SCC1=CC(CS)=C(CS)C=C1CS LJODQQVXMSKBHT-UHFFFAOYSA-N 0.000 description 1
- KLYZZKTYGAGJEC-UHFFFAOYSA-N [2,4,5-tris(sulfanylmethylsulfanyl)phenyl]sulfanylmethanethiol Chemical compound SCSC1=CC(SCS)=C(SCS)C=C1SCS KLYZZKTYGAGJEC-UHFFFAOYSA-N 0.000 description 1
- SUZMMPZZULWHPD-UHFFFAOYSA-N [2-(sulfanylmethoxy)phenoxy]methanethiol Chemical compound SCOC1=CC=CC=C1OCS SUZMMPZZULWHPD-UHFFFAOYSA-N 0.000 description 1
- YADAPEFZBBZQGC-UHFFFAOYSA-N [2-(sulfanylmethylsulfanyl)phenyl]sulfanylmethanethiol Chemical compound SCSC1=CC=CC=C1SCS YADAPEFZBBZQGC-UHFFFAOYSA-N 0.000 description 1
- BDVSVFDFAXCPQO-UHFFFAOYSA-N [3,4,5-tris(sulfanylmethoxy)phenoxy]methanethiol Chemical compound SCOC1=CC(OCS)=C(OCS)C(OCS)=C1 BDVSVFDFAXCPQO-UHFFFAOYSA-N 0.000 description 1
- WNXBCBXBGDOZCK-UHFFFAOYSA-N [3,4,5-tris(sulfanylmethyl)phenyl]methanethiol Chemical compound SCC1=CC(CS)=C(CS)C(CS)=C1 WNXBCBXBGDOZCK-UHFFFAOYSA-N 0.000 description 1
- VCQMOCQYLBOOQB-UHFFFAOYSA-N [3,4,5-tris(sulfanylmethylsulfanyl)phenyl]sulfanylmethanethiol Chemical compound SCSC1=CC(SCS)=C(SCS)C(SCS)=C1 VCQMOCQYLBOOQB-UHFFFAOYSA-N 0.000 description 1
- DSXMIKGNMNOMLL-UHFFFAOYSA-N [3,4-bis(sulfanylmethoxy)phenoxy]methanethiol Chemical compound SCOC1=CC=C(OCS)C(OCS)=C1 DSXMIKGNMNOMLL-UHFFFAOYSA-N 0.000 description 1
- OWDDXHQZWJBGMZ-UHFFFAOYSA-N [3,4-bis(sulfanylmethyl)phenyl]methanethiol Chemical compound SCC1=CC=C(CS)C(CS)=C1 OWDDXHQZWJBGMZ-UHFFFAOYSA-N 0.000 description 1
- OUSRZWDNEXRNIT-UHFFFAOYSA-N [3,4-bis(sulfanylmethylsulfanyl)phenyl]sulfanylmethanethiol Chemical compound SCSC1=CC=C(SCS)C(SCS)=C1 OUSRZWDNEXRNIT-UHFFFAOYSA-N 0.000 description 1
- CYVANFZTHHKUSB-UHFFFAOYSA-N [3,5-bis(sulfanylmethoxy)phenoxy]methanethiol Chemical compound SCOC1=CC(OCS)=CC(OCS)=C1 CYVANFZTHHKUSB-UHFFFAOYSA-N 0.000 description 1
- IPDLFYXRQIZSAD-UHFFFAOYSA-N [3,5-bis(sulfanylmethylsulfanyl)phenyl]sulfanylmethanethiol Chemical compound SCSC1=CC(SCS)=CC(SCS)=C1 IPDLFYXRQIZSAD-UHFFFAOYSA-N 0.000 description 1
- RUDUCNPHDIMQCY-UHFFFAOYSA-N [3-(2-sulfanylacetyl)oxy-2,2-bis[(2-sulfanylacetyl)oxymethyl]propyl] 2-sulfanylacetate Chemical compound SCC(=O)OCC(COC(=O)CS)(COC(=O)CS)COC(=O)CS RUDUCNPHDIMQCY-UHFFFAOYSA-N 0.000 description 1
- WWYGZBJGLPHDOT-UHFFFAOYSA-N [3-(sulfanylmethoxy)phenoxy]methanethiol Chemical compound SCOC1=CC=CC(OCS)=C1 WWYGZBJGLPHDOT-UHFFFAOYSA-N 0.000 description 1
- JSNABGZJVWSNOB-UHFFFAOYSA-N [3-(sulfanylmethyl)phenyl]methanethiol Chemical compound SCC1=CC=CC(CS)=C1 JSNABGZJVWSNOB-UHFFFAOYSA-N 0.000 description 1
- VLDJWLWRDVWISM-UHFFFAOYSA-N [3-(sulfanylmethylsulfanyl)-2,2-bis(sulfanylmethylsulfanylmethyl)propyl]sulfanylmethanethiol Chemical compound SCSCC(CSCS)(CSCS)CSCS VLDJWLWRDVWISM-UHFFFAOYSA-N 0.000 description 1
- WSAPARODZGDJER-UHFFFAOYSA-N [3-(sulfanylmethylsulfanyl)phenyl]sulfanylmethanethiol Chemical compound SCSC1=CC=CC(SCS)=C1 WSAPARODZGDJER-UHFFFAOYSA-N 0.000 description 1
- LVXYTKROCGJRNI-UHFFFAOYSA-N [4-(sulfanylmethoxy)phenoxy]methanethiol Chemical compound SCOC1=CC=C(OCS)C=C1 LVXYTKROCGJRNI-UHFFFAOYSA-N 0.000 description 1
- VGNFJJWLWFCHMR-UHFFFAOYSA-N [4-(sulfanylmethylsulfanyl)phenyl]sulfanylmethanethiol Chemical compound SCSC1=CC=C(SCS)C=C1 VGNFJJWLWFCHMR-UHFFFAOYSA-N 0.000 description 1
- 125000004018 acid anhydride group Chemical group 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- KHJIHSHHUDGOPQ-UHFFFAOYSA-N benzene-1,2,3,5-tetrathiol Chemical compound SC1=CC(S)=C(S)C(S)=C1 KHJIHSHHUDGOPQ-UHFFFAOYSA-N 0.000 description 1
- KVPDTCNNKWOGMZ-UHFFFAOYSA-N benzene-1,2,4,5-tetrathiol Chemical compound SC1=CC(S)=C(S)C=C1S KVPDTCNNKWOGMZ-UHFFFAOYSA-N 0.000 description 1
- KXCKKUIJCYNZAE-UHFFFAOYSA-N benzene-1,3,5-trithiol Chemical compound SC1=CC(S)=CC(S)=C1 KXCKKUIJCYNZAE-UHFFFAOYSA-N 0.000 description 1
- ZWOASCVFHSYHOB-UHFFFAOYSA-N benzene-1,3-dithiol Chemical compound SC1=CC=CC(S)=C1 ZWOASCVFHSYHOB-UHFFFAOYSA-N 0.000 description 1
- VRPKUXAKHIINGG-UHFFFAOYSA-N biphenyl-4,4'-dithiol Chemical group C1=CC(S)=CC=C1C1=CC=C(S)C=C1 VRPKUXAKHIINGG-UHFFFAOYSA-N 0.000 description 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
- KYNFOMQIXZUKRK-UHFFFAOYSA-N bishydroxyethyldisulfide Natural products OCCSSCCO KYNFOMQIXZUKRK-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- VSARMWHOISBCGR-UHFFFAOYSA-N cyclohexane-1,1-dithiol Chemical compound SC1(S)CCCCC1 VSARMWHOISBCGR-UHFFFAOYSA-N 0.000 description 1
- YKRCKUBKOIVILO-UHFFFAOYSA-N cyclohexane-1,2-dithiol Chemical compound SC1CCCCC1S YKRCKUBKOIVILO-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- UBAXRAHSPKWNCX-UHFFFAOYSA-N diallyl trisulfide Chemical group C=CCSSSCC=C UBAXRAHSPKWNCX-UHFFFAOYSA-N 0.000 description 1
- WQABCVAJNWAXTE-UHFFFAOYSA-N dimercaprol Chemical compound OCC(S)CS WQABCVAJNWAXTE-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- BITPLIXHRASDQB-UHFFFAOYSA-N ethenyl-[ethenyl(dimethyl)silyl]oxy-dimethylsilane Chemical compound C=C[Si](C)(C)O[Si](C)(C)C=C BITPLIXHRASDQB-UHFFFAOYSA-N 0.000 description 1
- 229940052303 ethers for general anesthesia Drugs 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- RVVRZLSZZKMJCB-UHFFFAOYSA-N heptane-1,7-dithiol Chemical compound SCCCCCCCS RVVRZLSZZKMJCB-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- UQQTZGJJERIOBT-UHFFFAOYSA-N hydroxymethylsulfanylmethanol Chemical compound OCSCO UQQTZGJJERIOBT-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 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
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KYAHXDQYSVFOOV-UHFFFAOYSA-N naphthalene-1,2-dithiol Chemical compound C1=CC=CC2=C(S)C(S)=CC=C21 KYAHXDQYSVFOOV-UHFFFAOYSA-N 0.000 description 1
- XMHBJPKFTZSWRJ-UHFFFAOYSA-N naphthalene-2,6-dithiol Chemical compound C1=C(S)C=CC2=CC(S)=CC=C21 XMHBJPKFTZSWRJ-UHFFFAOYSA-N 0.000 description 1
- INUVVGTZMFIDJF-UHFFFAOYSA-N naphthalene-2,7-dithiol Chemical compound C1=CC(S)=CC2=CC(S)=CC=C21 INUVVGTZMFIDJF-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- QYZLKGVUSQXAMU-UHFFFAOYSA-N penta-1,4-diene Chemical compound C=CCC=C QYZLKGVUSQXAMU-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- UKQMUPLYHOXQQR-UHFFFAOYSA-N phenylmethanedithiol Chemical compound SC(S)C1=CC=CC=C1 UKQMUPLYHOXQQR-UHFFFAOYSA-N 0.000 description 1
- PARWUHTVGZSQPD-UHFFFAOYSA-N phenylsilane Chemical compound [SiH3]C1=CC=CC=C1 PARWUHTVGZSQPD-UHFFFAOYSA-N 0.000 description 1
- IWWVYHZXNXEUPB-UHFFFAOYSA-N phenylsulfanylmethanethiol Chemical compound SCSC1=CC=CC=C1 IWWVYHZXNXEUPB-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002578 polythiourethane polymer Polymers 0.000 description 1
- 238000011417 postcuring Methods 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- RLJWTAURUFQFJP-UHFFFAOYSA-N propan-2-ol;titanium Chemical compound [Ti].CC(C)O.CC(C)O.CC(C)O.CC(C)O RLJWTAURUFQFJP-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- NCNISYUOWMIOPI-UHFFFAOYSA-N propane-1,1-dithiol Chemical compound CCC(S)S NCNISYUOWMIOPI-UHFFFAOYSA-N 0.000 description 1
- UWHMFGKZAYHMDJ-UHFFFAOYSA-N propane-1,2,3-trithiol Chemical compound SCC(S)CS UWHMFGKZAYHMDJ-UHFFFAOYSA-N 0.000 description 1
- ZJLMKPKYJBQJNH-UHFFFAOYSA-N propane-1,3-dithiol Chemical compound SCCCS ZJLMKPKYJBQJNH-UHFFFAOYSA-N 0.000 description 1
- HMPSOEYFMTWOFC-UHFFFAOYSA-N propane-2,2-dithiol Chemical compound CC(C)(S)S HMPSOEYFMTWOFC-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- ACTRVOBWPAIOHC-UHFFFAOYSA-N succimer Chemical compound OC(=O)C(S)C(S)C(O)=O ACTRVOBWPAIOHC-UHFFFAOYSA-N 0.000 description 1
- WTSBJMAOQNCZBF-UHFFFAOYSA-N sulfanylmethylsulfanylmethanethiol Chemical compound SCSCS WTSBJMAOQNCZBF-UHFFFAOYSA-N 0.000 description 1
- QNITWMBGUWZSSI-UHFFFAOYSA-N sulfanylmethylsulfanylmethylsulfanylmethanethiol Chemical compound SCSCSCS QNITWMBGUWZSSI-UHFFFAOYSA-N 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N tetraisopropyl titanate Substances CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- UVZICZIVKIMRNE-UHFFFAOYSA-N thiodiacetic acid Chemical compound OC(=O)CSCC(O)=O UVZICZIVKIMRNE-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- UDUKMRHNZZLJRB-UHFFFAOYSA-N triethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OCC)(OCC)OCC)CCC2OC21 UDUKMRHNZZLJRB-UHFFFAOYSA-N 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- UHUUYVZLXJHWDV-UHFFFAOYSA-N trimethyl(methylsilyloxy)silane Chemical compound C[SiH2]O[Si](C)(C)C UHUUYVZLXJHWDV-UHFFFAOYSA-N 0.000 description 1
- VOSUIKFOFHZNED-UHFFFAOYSA-N tris(prop-2-enyl) benzene-1,3,5-tricarboxylate Chemical compound C=CCOC(=O)C1=CC(C(=O)OCC=C)=CC(C(=O)OCC=C)=C1 VOSUIKFOFHZNED-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/04—Polythioethers from mercapto compounds or metallic derivatives thereof
- C08G75/045—Polythioethers from mercapto compounds or metallic derivatives thereof from mercapto compounds and unsaturated compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
(B)1分子中にSH基を少なくとも二つ有するチオール化合物(チオール化合物(B)ともいう。)、並びに、
(C)1分子中に炭素数2〜5のアルケニル基を少なくとも二つ有し、かつ、分子中に、(i)少なくとも一つの芳香環を含有する、及び/又は、(ii)(a)酸素原子、硫黄原子若しくはケイ素原子、若しくは、(b)炭素数2〜20(ただし、アルケニル基を構成する炭素を除く。)の鎖状若しくは非芳香環状の炭素鎖(ただし、炭素鎖を構成する炭素原子の一部が酸素原子、硫黄原子又はケイ素原子で置き換わっていてもよい。)のいずれかを少なくとも一つ含有する、アルケニル化合物(アルケニル化合物(C)ともいう。)を含有し、前記チタノキサン化合物(A)、チオール化合物(B)及びアルケニル化合物(C)は相溶溶液を形成することを特徴とする硬化性組成物である。本明細書中、アルケニル化合物とは広義に用いており、アルケニル基含有炭化水素、アルケニル基含有炭化水素誘導体を含む。
(D)1分子中にSH基を少なくとも二つ有し、かつ、分子中に、少なくとも一つの芳香環を含有する、及び/又は、炭素数3以上の鎖状若しくは非芳香環状の炭素鎖(ただし、炭素鎖を構成する炭素原子の一部が酸素原子、硫黄原子又はケイ素原子で置き換わっていてもよい。)を少なくとも一つ含有する、分子量200〜20,000のチオール化合物(チオール化合物(D)ともいう。)を含有し、前記チタノキサン化合物(A)及びチオール化合物(D)は相溶溶液を形成することを特徴とする硬化性組成物でもある。
TiαOβ(OR)γ (1)
式(1)中、Rは、炭素数1〜12のアルキル基である。分子中に複数存在するRは、それぞれ、同一でも異なっていてもよい。α、β、γは、以下の条件(a)〜(c)を満たし、αは正の整数、β、γは正の数である。
(a)80≧α≧2、
(b)1.8α≧β≧α、
(c)γ=4α−2β
以下、本発明を詳細に説明する。
また、一般に、チオール化合物(B)が多いと製膜性が高く、アルケニル化合物(C)が多いと硬化物の透明性が高くなるが、製膜性と透明性の高い水準でのバランスを考慮すると、チオール化合物(B)とアルケニル化合物(C)との配合比(重量比)は、5:95〜95:5が好ましく、10:90〜90:10がより好ましい。
また、上記チタノキサン化合物(A)とチオール化合物(D)の合計量に対するチタノキサン化合物(A)の配合量は50〜95重量%が好ましく、65〜90重量%がより好ましい。
界面活性剤としては、例えば、メガファックR−08(商品名)、メガファックF−410(商品名)(いずれも大日本インキ化学工業社製)、EF−102(商品名)(株式会社ジェムコ製)等が挙げられる。
ヒンダードアミン系光安定化剤としては、例えば、TINUVIN(登録商標)770、TINUVIN(登録商標)622LD(いずれもチバスペシャルティーケミカルズ社製)、アデカスタブ(登録商標)LA−57(旭電化工業社製)等が挙げられる。
ヒンダードフェノール系酸化防止剤としては、例えば、IRGANOX(登録商標)1010(チバスペシャルティーケミカルズ社製)、ノクラックNS−30(商品名)(大内新興化学工業社製)、トミノックスTT(商品名)(吉豊ファインケミカル社製)等が挙げられる。
上記ヒンダードアミン系光安定化剤の配合量は、組成物中、0.01〜0.5phrが好ましく、より好ましくは0.1〜0.3phrである。
上記ヒンダードフェノール系酸化防止剤の配合量は、組成物中、0.01〜0.5phrが好ましく、より好ましくは0.1〜0.3phrである。
ポリチタノキサンの合成
回転子、還流管、滴下ロートを備えた三つ口ナス型フラスコにイソプロピルアルコール22.72gとテトライソプロピルチタネート22.72g(0.08mol)を仕込み、よく撹拌しながら80℃で加温保持した。この中に蒸留水2.30g(0.128mol)とイソプロピルアルコール34.56gとの混合液を徐々に滴下した後、85℃で2時間還流し、反応を熟成させた。反応液を冷却した後、アスピレーターを用いて濃縮し、白色固体(Ti含有量39.9%)9.60gを得た。式(1)におけるα、β、γの理論値は、α=10、β=16、γ=8である。
表1に示す各成分及び組成(重量部)でそれぞれ配合し25℃で混合し、均一な液状組成物を調製した。得られた各組成物をガラス基板上にスピンコートした後、それぞれ、下記の条件で硬化させて硬化物を得た。得られた硬化物の膜厚、透過率およびヘーズ値を下記のとおり評価した。また得られた各組成物をシリコンウエハ上にスピンコートした後、それぞれ、下記の条件で硬化させて硬化物を得た。得られた屈折率を下記のとおり評価した。結果を表1に示した。
SH基含有化合物とアルケニル基含有化合物とを予め反応させた有機化合物を化合物(D)として、表1、表2に示す成分を用い、実施例1と同様にして混合し、均一な液状組成物を調製し、硬化物を得た。
表1の配合を用いたこと以外は実施例1と同様にして組成物を調製し、硬化物を得た。
評価
測定条件は以下のとおり。
厚み測定:触針式表面形状測定器
透過率:ダブルビーム式ヘーズコンピューターを用い、ガラス基板の硬化膜の透過率を測定した。標準には硬化性組成物塗布前のガラス基板を使用した。
ヘーズ値:ガラス基板上の硬化膜の曇度をダブルビーム式ヘーズコンピューターにて測定した。標準には硬化性組成物塗布前のガラス基板を使用した。
熱硬化性:加熱後ガラス基板上の硬化物についてクラックの有無を、それぞれ目視にて観察した。
評価基準は以下のとおり。
○:クラック無し、△:クラック発生、×:剥離発生
屈折率の測定:エリプソメーターを用いて632.3nmにおける屈折率を25℃にて測定した。
ポリチタノキサン(A):製造例1で得られたポリチタノキサン
SH基含有化合物(B)(1):4,4’−チオビスベンゼンチオール
SH基含有化合物(B)(2):ペンタエリスリトールテトラキス(3−メルカプトプロピオネート)
SH基含有化合物(B)(3):1,4−ジメルカプトベンゼン
SH基含有化合物(B)(4):2,2′−(エチレンジチオ)ジエタンチオール
SH基含有化合物(B)(5):1,5−ナフタレンジチオール
SH基含有化合物(B)(6):1,4−ビス(メルカプトメチル)ベンゼン
アルケニル基含有機化合物(C)(1):次のオリゴマー:フタル酸ジアリル/1,4−ビス(ジメチルシリル)ベンゼンのモル比2:1で配合しヒドロシリル化反応によって得られたアルケニル基含有有機化合物(分子量:1090)
アルケニル基含有機化合物(C)(2):ペンタエリスリトールテトラアリルエーテル
アルケニル基含有機化合物(C)(3):次のオリゴマー:フタル酸ジアリル/ジフェニルシランをモル比2:1で配合し、ヒドロシリル化反応によって得られたアルケニル基含有有機化合物(分子量:930)
アルケニル基含有機化合物(C)(4):次のオリゴマー:アジピン酸ジビニル/1,4−ビス(ジメチルシリル)ベンゼンをモル比2:1で配合し、ヒドロシリル化反応によって得られたアルケニル基含有有機化合物(分子量:1200)
アルケニル基含有機化合物(C)(5):次のオリゴマー:ジビニルベンゼン/1,4−ビス(ジメチルシリル)ベンゼンをモル比2:1で配合し、ヒドロシリル化反応によって得られたアルケニル基含有有機化合物(分子量:2350)
アルケニル基含有機化合物(C)(6):次のオリゴマー:ジビニルベンゼン/4,4′−チオビスベンゼンチオールをモル比2:1で配合して得た付加反応物(分子量:1500)
アルケニル基含有機化合物(C)(7):次のオリゴマー:アジピン酸ジビニル/4,4′−チオビスベンゼンチオールをモル比2:1で配合して得た付加反応物(分子量:1850)
アルケニル基含有機化合物(C)(8):次のオリゴマー:1,8−ノナジエン/4,4′−チオビスベンゼンチオールをモル比2:1で配合して得た付加反応物(分子量:3620)
アルケニル基含有機化合物(C)(9):次のオリゴマー:ジアリルジカーボネート/4,4′−チオビスベンゼンチオールをモル比2:1で配合して得た付加反応物(分子量:1950)
化合物(D)(1):次のオリゴマー:4,4′−チオビスベンゼンチオール/フタル酸ジアリルのモル比2:1で配合した付加反応物(分子量:2260)
化合物(D)(2):次のオリゴマー:1,4−ベンゼンチオール/フタル酸ジアリルのモル比2:1で配合した付加反応物(分子量:3000)
化合物(D)(3):次のオリゴマー:1,4−ビス(メルカプトメチル)ベンゼン/フタル酸ジアリルのモル比2:1で配合した付加反応物(分子量:2260)
化合物(D)(4):次のオリゴマー:1,5−ナフタレンジチオール/フタル酸ジアリルのモル比2:1で配合した付加反応物(分子量:3300)
化合物(D)(5):次のオリゴマー:2,2’−(エチレンジチオ)ジエタンチオール/トリメチロールプロパントリアリルエーテルのモル比3:1で配合した付加反応物(分子量:未測定)
化合物(D)(6):次のオリゴマー:4,4′−チオビスベンゼンチオール/アジピン酸ジビニルのモル比2:1で配合した付加反応物(分子量:2120)
Claims (17)
- (A)チタンテトラアルコキシドを1.0〜1.8倍モルの量の水を用いて加水分解縮合させて得られるチタノキサン化合物、
(B)1分子中にSH基を少なくとも二つ有するチオール化合物、並びに、
(C)1分子中に炭素数2〜5のアルケニル基を少なくとも二つ有し、かつ、分子中に、(i)少なくとも一つの芳香環を含有する、及び/又は、(ii)(a)酸素原子、硫黄原子若しくはケイ素原子、若しくは、(b)炭素数2〜20(ただし、アルケニル基を構成する炭素を除く。)の鎖状若しくは非芳香環状の炭素鎖(ただし、炭素鎖を構成する炭素原子の一部が酸素原子、硫黄原子又はケイ素原子で置き換わっていてもよい。)のいずれかを少なくとも一つ含有する、アルケニル化合物を含有し、前記チタノキサン化合物(A)、チオール化合物(B)及びアルケニル化合物(C)は相溶溶液を形成することを特徴とする硬化性組成物。 - チオール化合物(B)は、分子中に、少なくとも一つの芳香環を含有する、及び/又は、直鎖状、分枝鎖状若しくは脂環状の、炭素数2〜20の炭素鎖(ただし、炭素鎖を構成する炭素原子の一部が酸素原子、硫黄原子又はケイ素原子で置き換わっていてもよい。)を少なくとも一つ含有する、チオール化合物である請求項1記載の組成物。
- チオール化合物(B)は、芳香族チオール、チオール基以外に硫黄原子を有する芳香族チオール、脂肪族チオール及びチオール基以外に硫黄原子を有する脂肪族チオール又は非芳香環含有チオールからなる群から選択される少なくとも1種のチオールである請求項1又は2記載の組成物。
- チオール化合物(B)は、SH基当量が1000g/eq以下のものである請求項1〜3のいずれか記載の組成物。
- チオール化合物(B)は、(エチレンジチオ)ジエタンチオール、ジメルカプトベンゼン、ビス(メルカプトメチル)ベンゼン、ナフタレンジチオール、ベンゼントリチオール、チオビスベンゼンチオール、トリメチロールプロパントリス(3−メルカプトプロピオネート)、及びペンタエリスリトールテトラキス(3−メルカプトプロピオネート)からなる群から選択される少なくとも1種である請求項3又は4記載の組成物。
- チオール化合物(B)は、ジメルカプトベンゼン、ビス(メルカプトメチル)ベンゼン、ベンゼントリチオール、ナフタレンジチオール及びチオビスベンゼンチオールからなる群から選択される少なくとも1種である請求項5記載の組成物。
- アルケニル化合物(C)は、アルケニル基としてビニル基又はアリル基を含有するものである請求項1〜6のいずれか記載の組成物。
- アルケニル化合物(C)は、脂肪族アルケニル化合物、炭素以外に酸素原子、イオウ原子又はケイ素原子を含有する脂肪族又は非芳香環含有アルケニル化合物、芳香族アルケニル化合物、炭素以外に酸素原子、イオウ原子又はケイ素原子を含有する芳香族アルケニル化合物からなる群から選択される少なくとも1種のアルケニル化合物である請求項1〜7のいずれか記載の組成物。
- アルケニル化合物(C)は、芳香環としてベンゼン環を含有するものである請求項1〜8のいずれか記載の組成物。
- アルケニル化合物(C)は、ジビニルベンゼン、ジアリルベンゼン、トリビニルベンゼン、テトラアリルベンゼン、へキサアリルベンゼン、ジビニルトルエン、ビスフェノールAジアリルエーテル、ジアリルオキシベンゼン、テレフタル酸ジアリル、フタル酸ジアリル、イソフタル酸ジアリル、トリメリット酸ジアリル、トリメリット酸トリアリル、ピロメリット酸トリアリル、ピロメリット酸テトラアリル、ビス(ジメチルビニルシリル)ベンゼン、ジビニルメチルフェニルシラン、ジビニルジフェニルシラン及びジアリルジフェニルシランからなる群から選択される少なくとも1種である請求項9記載の組成物。
- アルケニル化合物(C)は、1分子中にヒドロシリル基を少なくとも二つ有する有機化合物と1分子中にアルケニル基を少なくとも二つ有する有機化合物とからヒドロシリル化反応によって鎖伸張されたアルケニル基含有機化合物、及び、1分子中にSH基を少なくとも二つ有する有機化合物と1分子中にアルケニル基を少なくとも二つ有する有機化合物とから付加反応によって鎖伸張されたアルケニル基含有化合物からなる群から選択される少なくとも1種である請求項1〜9のいずれか記載の組成物。
- (A)チタンテトラアルコキシドを1.0〜1.8倍モルの量の水を用いて加水分解縮合させて得られるチタノキサン化合物、並びに、
(D)1分子中にSH基を少なくとも二つ有し、かつ、分子中に、少なくとも一つの芳香環を含有する、及び/又は、炭素数3以上の鎖状若しくは非芳香環状の炭素鎖(ただし、炭素鎖を構成する炭素原子の一部が酸素原子、硫黄原子又はケイ素原子で置き換わっていてもよい。)を少なくとも一つ含有する、分子量300〜20,000のチオール化合物を含有し、前記チタノキサン化合物(A)及びチオール化合物(D)は相溶溶液を形成することを特徴とする硬化性組成物。 - チオール化合物(D)は、(B)1分子中にSH基を少なくとも二つ有するチオール化合物と(C)1分子中に炭素数2〜5のアルケニル基を少なくとも二つ有し、かつ、分子中に、(i)少なくとも一つの芳香環を含有する、及び/又は、(ii)(a)酸素原子、硫黄原子若しくはケイ素原子、若しくは、(b)炭素数2(ただし、アルケニル基を構成する炭素を除く。)以上の鎖状若しくは非芳香環状の炭素鎖(ただし、炭素鎖を構成する炭素原子の一部が酸素原子、硫黄原子又はケイ素原子で置き換わっていてもよい。)のいずれかを少なくとも一つ含有する、アルケニル化合物とを反応させたチオール化合物である請求項12記載の組成物。
- チオール化合物(D)は、芳香環としてベンゼン環を含有するものである請求項12又は13記載の組成物。
- チタノキサン化合物(A)は、下記一般式(1)で表される化合物である請求項1〜11のいずれか記載の組成物:
TiαOβ(OR)γ (1)
[式(1)中、Rは、炭素数1〜12のアルキル基である。分子中に複数存在するRは、それぞれ、同一でも異なっていてもよい。α、β、γは、以下の条件(a)〜(c)を満たし、αは正の整数、β、γは正の数である:
(a)80≧α≧2、
(b)1.8α≧β≧α、
(c)γ=4α−2β]。 - チタノキサン化合物(A)は、下記一般式(1)で表される化合物である請求項12〜14のいずれか記載の組成物:
TiαOβ(OR)γ (1)
[式(1)中、Rは、炭素数1〜12のアルキル基である。分子中に複数存在するRは、それぞれ、同一でも異なっていてもよい。α、β、γは、以下の条件(a)〜(c)を満たし、αは正の整数、β、γは正の数である:
(a)80≧α≧2、
(b)1.8α≧β≧α、
(c)γ=4α−2β]。 - チタノキサン化合物(A)を、チタノキサン化合物(A)、チオール化合物(B)及びアルケニル化合物(C)の合計に対して、50〜95重量%含有する請求項1〜11、15のいずれか記載の組成物。
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