JP5301164B2 - チオール化合物を含有する硬化性組成物 - Google Patents
チオール化合物を含有する硬化性組成物 Download PDFInfo
- Publication number
- JP5301164B2 JP5301164B2 JP2007555996A JP2007555996A JP5301164B2 JP 5301164 B2 JP5301164 B2 JP 5301164B2 JP 2007555996 A JP2007555996 A JP 2007555996A JP 2007555996 A JP2007555996 A JP 2007555996A JP 5301164 B2 JP5301164 B2 JP 5301164B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- curable composition
- formula
- compound
- composition according
- 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.)
- Active
Links
- -1 thiol compound Chemical class 0.000 title claims abstract description 125
- 239000000203 mixture Substances 0.000 title claims abstract description 72
- 150000001875 compounds Chemical class 0.000 claims description 47
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 36
- 125000003118 aryl group Chemical group 0.000 claims description 30
- 125000004432 carbon atom Chemical group C* 0.000 claims description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 21
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 229910052717 sulfur Inorganic materials 0.000 claims description 19
- 125000004434 sulfur atom Chemical group 0.000 claims description 18
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 16
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 16
- 125000001931 aliphatic group Chemical group 0.000 claims description 15
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 15
- 125000000623 heterocyclic group Chemical group 0.000 claims description 15
- 125000002947 alkylene group Chemical group 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 10
- 239000003999 initiator Substances 0.000 claims description 10
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims description 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 9
- UUAGPGQUHZVJBQ-UHFFFAOYSA-N Bisphenol A bis(2-hydroxyethyl)ether Chemical compound C=1C=C(OCCO)C=CC=1C(C)(C)C1=CC=C(OCCO)C=C1 UUAGPGQUHZVJBQ-UHFFFAOYSA-N 0.000 claims description 7
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 7
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 6
- BXGYYDRIMBPOMN-UHFFFAOYSA-N 2-(hydroxymethoxy)ethoxymethanol Chemical compound OCOCCOCO BXGYYDRIMBPOMN-UHFFFAOYSA-N 0.000 claims description 5
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 claims description 5
- NQXNYVAALXGLQT-UHFFFAOYSA-N 2-[4-[9-[4-(2-hydroxyethoxy)phenyl]fluoren-9-yl]phenoxy]ethanol Chemical compound C1=CC(OCCO)=CC=C1C1(C=2C=CC(OCCO)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 NQXNYVAALXGLQT-UHFFFAOYSA-N 0.000 claims description 4
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims description 3
- 235000011187 glycerol Nutrition 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 claims description 2
- 239000000463 material Substances 0.000 description 25
- 238000000576 coating method Methods 0.000 description 15
- 239000011248 coating agent Substances 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 13
- 230000009257 reactivity Effects 0.000 description 13
- 230000003287 optical effect Effects 0.000 description 12
- 239000003505 polymerization initiator Substances 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 9
- 238000011156 evaluation Methods 0.000 description 9
- 238000005259 measurement Methods 0.000 description 9
- 239000003973 paint Substances 0.000 description 8
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 8
- 238000007259 addition reaction Methods 0.000 description 7
- 150000002148 esters Chemical group 0.000 description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
- HOXINJBQVZWYGZ-UHFFFAOYSA-N fenbutatin oxide Chemical compound C=1C=CC=CC=1C(C)(C)C[Sn](O[Sn](CC(C)(C)C=1C=CC=CC=1)(CC(C)(C)C=1C=CC=CC=1)CC(C)(C)C=1C=CC=CC=1)(CC(C)(C)C=1C=CC=CC=1)CC(C)(C)C1=CC=CC=C1 HOXINJBQVZWYGZ-UHFFFAOYSA-N 0.000 description 7
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 238000002834 transmittance Methods 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 6
- 238000001723 curing Methods 0.000 description 6
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 6
- 229910052753 mercury Inorganic materials 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 239000011342 resin composition Substances 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 229920001187 thermosetting polymer Polymers 0.000 description 5
- JDGWMLZPJJXMCC-UHFFFAOYSA-N 3-phenyl-3-sulfanylpropanoic acid Chemical compound OC(=O)CC(S)C1=CC=CC=C1 JDGWMLZPJJXMCC-UHFFFAOYSA-N 0.000 description 4
- RQPNXPWEGVCPCX-UHFFFAOYSA-N 3-sulfanylbutanoic acid Chemical compound CC(S)CC(O)=O RQPNXPWEGVCPCX-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 150000002009 diols Chemical class 0.000 description 4
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 238000007639 printing Methods 0.000 description 4
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 4
- 238000010526 radical polymerization reaction Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000012719 thermal polymerization Methods 0.000 description 4
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- JTMBCYAUSCBSEY-UHFFFAOYSA-N 2-methyl-2-sulfanylpropanoic acid Chemical compound CC(C)(S)C(O)=O JTMBCYAUSCBSEY-UHFFFAOYSA-N 0.000 description 3
- MHRDCHHESNJQIS-UHFFFAOYSA-N 2-methyl-3-sulfanylpropanoic acid Chemical compound SCC(C)C(O)=O MHRDCHHESNJQIS-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- JMMSLMMJRMCXPW-UHFFFAOYSA-N OC.OC.C1CC2CCC1C2 Chemical compound OC.OC.C1CC2CCC1C2 JMMSLMMJRMCXPW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 3
- 125000001033 ether group Chemical group 0.000 description 3
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000012778 molding material Substances 0.000 description 3
- 239000013307 optical fiber Substances 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 150000004291 polyenes Chemical class 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 229920006295 polythiol Polymers 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- CKHMBZDXZKPAKT-UHFFFAOYSA-N (2-isocyanatophenyl) prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1N=C=O CKHMBZDXZKPAKT-UHFFFAOYSA-N 0.000 description 2
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 2
- BPXVHIRIPLPOPT-UHFFFAOYSA-N 1,3,5-tris(2-hydroxyethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound OCCN1C(=O)N(CCO)C(=O)N(CCO)C1=O BPXVHIRIPLPOPT-UHFFFAOYSA-N 0.000 description 2
- 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 2
- DPNXHTDWGGVXID-UHFFFAOYSA-N 2-isocyanatoethyl prop-2-enoate Chemical compound C=CC(=O)OCCN=C=O DPNXHTDWGGVXID-UHFFFAOYSA-N 0.000 description 2
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 description 2
- PMNLUUOXGOOLSP-UHFFFAOYSA-M 2-sulfanylpropanoate Chemical compound CC(S)C([O-])=O PMNLUUOXGOOLSP-UHFFFAOYSA-M 0.000 description 2
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 2
- PTPQZNNAUUSACC-UHFFFAOYSA-N 3-sulfanylpentanoic acid Chemical compound CCC(S)CC(O)=O PTPQZNNAUUSACC-UHFFFAOYSA-N 0.000 description 2
- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 2
- NEAFWRKPYYJETG-UHFFFAOYSA-N 4-sulfanylpentanoic acid Chemical compound CC(S)CCC(O)=O NEAFWRKPYYJETG-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000006356 dehydrogenation reaction Methods 0.000 description 2
- 239000005548 dental material Substances 0.000 description 2
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 239000012776 electronic material Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000000976 ink Substances 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 229910001507 metal halide Inorganic materials 0.000 description 2
- 150000005309 metal halides Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 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 2
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 2
- 229960004063 propylene glycol Drugs 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 description 2
- QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 1
- ZQIKFDMUXNPPAD-UHFFFAOYSA-N (2-isocyanato-3-prop-2-enoyloxypropyl) prop-2-enoate Chemical compound C=CC(=O)OCC(N=C=O)COC(=O)C=C ZQIKFDMUXNPPAD-UHFFFAOYSA-N 0.000 description 1
- ZORJPNCZZRLEDF-UHFFFAOYSA-N (3-methoxy-3-methylbutoxy)carbonyloxy (3-methoxy-3-methylbutyl) carbonate Chemical compound COC(C)(C)CCOC(=O)OOC(=O)OCCC(C)(C)OC ZORJPNCZZRLEDF-UHFFFAOYSA-N 0.000 description 1
- NOBYOEQUFMGXBP-UHFFFAOYSA-N (4-tert-butylcyclohexyl) (4-tert-butylcyclohexyl)oxycarbonyloxy carbonate Chemical compound C1CC(C(C)(C)C)CCC1OC(=O)OOC(=O)OC1CCC(C(C)(C)C)CC1 NOBYOEQUFMGXBP-UHFFFAOYSA-N 0.000 description 1
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
- 0 **C(NCCCCOC(C(*)=C)=O)=O Chemical compound **C(NCCCCOC(C(*)=C)=O)=O 0.000 description 1
- GJZFGDYLJLCGHT-UHFFFAOYSA-N 1,2-diethylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=C(CC)C(CC)=CC=C3SC2=C1 GJZFGDYLJLCGHT-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- ILVWNAMWRGLVJO-UHFFFAOYSA-N 1-(2-methyl-2-sulfanylpropanoyl)oxybutyl 2-methyl-2-sulfanylpropanoate Chemical compound CC(S)(C)C(=O)OC(CCC)OC(=O)C(C)(C)S ILVWNAMWRGLVJO-UHFFFAOYSA-N 0.000 description 1
- RQQLOWXQARLAAX-UHFFFAOYSA-N 1-(2-methyl-3-sulfanylpropanoyl)oxybutyl 2-methyl-3-sulfanylpropanoate Chemical compound SCC(C)C(=O)OC(CCC)OC(=O)C(C)CS RQQLOWXQARLAAX-UHFFFAOYSA-N 0.000 description 1
- PCYWJMHMCPJIOY-UHFFFAOYSA-N 1-(2-sulfanylbutoxy)butane-2-thiol Chemical group CCC(S)COCC(S)CC PCYWJMHMCPJIOY-UHFFFAOYSA-N 0.000 description 1
- FFKMOERMMSQOAJ-UHFFFAOYSA-N 1-(2-sulfanylpropoxy)propane-2-thiol Chemical group CC(S)COCC(C)S FFKMOERMMSQOAJ-UHFFFAOYSA-N 0.000 description 1
- FHBPPCNSKZPLKT-UHFFFAOYSA-N 1-(3-phenyl-3-sulfanylpropanoyl)oxybutyl 3-phenyl-3-sulfanylpropanoate Chemical compound C=1C=CC=CC=1C(S)CC(=O)OC(CCC)OC(=O)CC(S)C1=CC=CC=C1 FHBPPCNSKZPLKT-UHFFFAOYSA-N 0.000 description 1
- UYWJYQBUSUMZDF-UHFFFAOYSA-N 1-(3-sulfanylbutanoyloxy)butyl 3-sulfanylbutanoate Chemical compound CC(S)CC(=O)OC(CCC)OC(=O)CC(C)S UYWJYQBUSUMZDF-UHFFFAOYSA-N 0.000 description 1
- NNPCVQRRYRVUOC-UHFFFAOYSA-N 1-(3-sulfanylpentanoyloxy)butyl 3-sulfanylpentanoate Chemical compound CCC(S)CC(=O)OC(CCC)OC(=O)CC(S)CC NNPCVQRRYRVUOC-UHFFFAOYSA-N 0.000 description 1
- PESCXBALTVVUFX-UHFFFAOYSA-N 1-(4-sulfanylpentanoyloxy)butyl 4-sulfanylpentanoate Chemical compound CC(S)CCC(=O)OC(CCC)OC(=O)CCC(C)S PESCXBALTVVUFX-UHFFFAOYSA-N 0.000 description 1
- JBCNOZAOTZSHGM-UHFFFAOYSA-N 1-[4-(1-sulfanylethyl)phenyl]ethanethiol Chemical compound CC(S)C1=CC=C(C(C)S)C=C1 JBCNOZAOTZSHGM-UHFFFAOYSA-N 0.000 description 1
- GAGZMZMLWYGJJJ-UHFFFAOYSA-N 2,2-bis(2-sulfanylpropanoyloxymethyl)butyl 2-sulfanylpropanoate Chemical compound CC(S)C(=O)OCC(CC)(COC(=O)C(C)S)COC(=O)C(C)S GAGZMZMLWYGJJJ-UHFFFAOYSA-N 0.000 description 1
- NSGOYQMHMLWQPM-UHFFFAOYSA-N 2-(2,2-dihydroxyethoxy)ethane-1,1-diol;3-sulfanylbutanoic acid Chemical compound CC(S)CC(O)=O.OC(O)COCC(O)O NSGOYQMHMLWQPM-UHFFFAOYSA-N 0.000 description 1
- CHKCPIUYSMYEEW-UHFFFAOYSA-N 2-(2-cyclohexylpropan-2-ylperoxy)-2-ethylhexanoic acid Chemical compound CCCCC(CC)(C(O)=O)OOC(C)(C)C1CCCCC1 CHKCPIUYSMYEEW-UHFFFAOYSA-N 0.000 description 1
- WQECNJBUYKDLGS-UHFFFAOYSA-N 2-(2-methyl-2-sulfanylpropanoyl)oxyethyl 2-methyl-2-sulfanylpropanoate Chemical compound CC(C)(S)C(=O)OCCOC(=O)C(C)(C)S WQECNJBUYKDLGS-UHFFFAOYSA-N 0.000 description 1
- ZUWFDHPIBGDTSU-UHFFFAOYSA-N 2-(2-methyl-2-sulfanylpropanoyl)oxypropyl 2-methyl-2-sulfanylpropanoate Chemical compound CC(S)(C)C(=O)OC(C)COC(=O)C(C)(C)S ZUWFDHPIBGDTSU-UHFFFAOYSA-N 0.000 description 1
- JUKSUBINMNCBNL-UHFFFAOYSA-N 2-(2-methyl-3-sulfanylpropanoyl)oxyethyl 2-methyl-3-sulfanylpropanoate Chemical compound SCC(C)C(=O)OCCOC(=O)C(C)CS JUKSUBINMNCBNL-UHFFFAOYSA-N 0.000 description 1
- OUNXABDTPQONBC-UHFFFAOYSA-N 2-(2-methyl-3-sulfanylpropanoyl)oxypropyl 2-methyl-3-sulfanylpropanoate Chemical compound SCC(C)C(=O)OC(C)COC(=O)C(C)CS OUNXABDTPQONBC-UHFFFAOYSA-N 0.000 description 1
- CNDCQWGRLNGNNO-UHFFFAOYSA-N 2-(2-sulfanylethoxy)ethanethiol Chemical group SCCOCCS CNDCQWGRLNGNNO-UHFFFAOYSA-N 0.000 description 1
- SDOLXVNBYQTXKO-UHFFFAOYSA-N 2-(2-sulfanylpropanoyloxy)ethyl 2-sulfanylpropanoate Chemical compound CC(S)C(=O)OCCOC(=O)C(C)S SDOLXVNBYQTXKO-UHFFFAOYSA-N 0.000 description 1
- YYOPQPVSBDLOBR-UHFFFAOYSA-N 2-(2-sulfanylpropanoyloxy)propyl 2-sulfanylpropanoate Chemical compound CC(S)C(=O)OCC(C)OC(=O)C(C)S YYOPQPVSBDLOBR-UHFFFAOYSA-N 0.000 description 1
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 1
- UBFKIKQPFXKIFS-UHFFFAOYSA-N 2-(3-methyl-4-sulfanylbutanoyl)oxypropyl 3-methyl-4-sulfanylbutanoate Chemical compound SCC(C)CC(=O)OCC(C)OC(=O)CC(C)CS UBFKIKQPFXKIFS-UHFFFAOYSA-N 0.000 description 1
- UXVINRUFDWQENP-UHFFFAOYSA-N 2-(3-phenyl-3-sulfanylpropanoyl)oxyethyl 3-phenyl-3-sulfanylpropanoate Chemical compound C=1C=CC=CC=1C(S)CC(=O)OCCOC(=O)CC(S)C1=CC=CC=C1 UXVINRUFDWQENP-UHFFFAOYSA-N 0.000 description 1
- JTRWFWDAJIZJJY-UHFFFAOYSA-N 2-(3-phenyl-3-sulfanylpropanoyl)oxypropyl 3-phenyl-3-sulfanylpropanoate Chemical compound C=1C=CC=CC=1C(S)CC(=O)OC(C)COC(=O)CC(S)C1=CC=CC=C1 JTRWFWDAJIZJJY-UHFFFAOYSA-N 0.000 description 1
- TXJZAWRTHMZECY-UHFFFAOYSA-N 2-(3-sulfanylbutanoyloxy)ethyl 3-sulfanylbutanoate Chemical compound CC(S)CC(=O)OCCOC(=O)CC(C)S TXJZAWRTHMZECY-UHFFFAOYSA-N 0.000 description 1
- KQBUONNTLMDRIE-UHFFFAOYSA-N 2-(3-sulfanylbutanoyloxy)propyl 3-sulfanylbutanoate Chemical compound CC(S)CC(=O)OCC(C)OC(=O)CC(C)S KQBUONNTLMDRIE-UHFFFAOYSA-N 0.000 description 1
- LDVVGHWJTSBTSL-UHFFFAOYSA-N 2-(3-sulfanylpentanoyloxy)ethyl 3-sulfanylpentanoate Chemical compound CCC(S)CC(=O)OCCOC(=O)CC(S)CC LDVVGHWJTSBTSL-UHFFFAOYSA-N 0.000 description 1
- ZVLHJMYLLYRAED-UHFFFAOYSA-N 2-(3-sulfanylpentanoyloxy)propyl 3-sulfanylpentanoate Chemical compound CCC(S)CC(=O)OCC(C)OC(=O)CC(S)CC ZVLHJMYLLYRAED-UHFFFAOYSA-N 0.000 description 1
- XJVUIQYBEPGDTH-UHFFFAOYSA-N 2-(4-sulfanylpentanoyloxy)ethyl 4-sulfanylpentanoate Chemical compound CC(S)CCC(=O)OCCOC(=O)CCC(C)S XJVUIQYBEPGDTH-UHFFFAOYSA-N 0.000 description 1
- GJKGAPPUXSSCFI-UHFFFAOYSA-N 2-Hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone Chemical compound CC(C)(O)C(=O)C1=CC=C(OCCO)C=C1 GJKGAPPUXSSCFI-UHFFFAOYSA-N 0.000 description 1
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
- LVOWEXPQXNYTLG-UHFFFAOYSA-N 2-[2-(2-methyl-2-sulfanylpropanoyl)oxyethoxy]ethyl 2-methyl-2-sulfanylpropanoate Chemical compound CC(C)(S)C(=O)OCCOCCOC(=O)C(C)(C)S LVOWEXPQXNYTLG-UHFFFAOYSA-N 0.000 description 1
- DQVMFULYAVKKQJ-UHFFFAOYSA-N 2-[2-(2-methyl-3-sulfanylpropanoyl)oxyethoxy]ethyl 2-methyl-3-sulfanylpropanoate Chemical compound SCC(C)C(=O)OCCOCCOC(=O)C(C)CS DQVMFULYAVKKQJ-UHFFFAOYSA-N 0.000 description 1
- IJVMLVYWDWJACR-UHFFFAOYSA-N 2-[2-(2-sulfanylpropanoyloxy)ethoxy]ethyl 2-sulfanylpropanoate Chemical compound CC(S)C(=O)OCCOCCOC(=O)C(C)S IJVMLVYWDWJACR-UHFFFAOYSA-N 0.000 description 1
- YOVMPJJCQAOBGV-UHFFFAOYSA-N 2-[2-(3-phenyl-3-sulfanylpropanoyl)oxyethoxy]ethyl 3-phenyl-3-sulfanylpropanoate Chemical compound C=1C=CC=CC=1C(S)CC(=O)OCCOCCOC(=O)CC(S)C1=CC=CC=C1 YOVMPJJCQAOBGV-UHFFFAOYSA-N 0.000 description 1
- SZAOTLOVASMEHW-UHFFFAOYSA-N 2-[2-(3-sulfanylbutanoyloxy)ethoxy]ethyl 3-sulfanylbutanoate Chemical compound CC(S)CC(=O)OCCOCCOC(=O)CC(C)S SZAOTLOVASMEHW-UHFFFAOYSA-N 0.000 description 1
- SOXVWNSYWOAERH-UHFFFAOYSA-N 2-[2-(3-sulfanylpentanoyloxy)ethoxy]ethyl 3-sulfanylpentanoate Chemical compound CCC(S)CC(=O)OCCOCCOC(=O)CC(S)CC SOXVWNSYWOAERH-UHFFFAOYSA-N 0.000 description 1
- DFBWSGKQKVHHBF-UHFFFAOYSA-N 2-[2-(4-sulfanylpentanoyloxy)ethoxy]ethyl 4-sulfanylpentanoate Chemical compound CC(S)CCC(=O)OCCOCCOC(=O)CCC(C)S DFBWSGKQKVHHBF-UHFFFAOYSA-N 0.000 description 1
- UHFFVFAKEGKNAQ-UHFFFAOYSA-N 2-benzyl-2-(dimethylamino)-1-(4-morpholin-4-ylphenyl)butan-1-one Chemical compound C=1C=C(N2CCOCC2)C=CC=1C(=O)C(CC)(N(C)C)CC1=CC=CC=C1 UHFFVFAKEGKNAQ-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- VGZZAZYCLRYTNQ-UHFFFAOYSA-N 2-ethoxyethoxycarbonyloxy 2-ethoxyethyl carbonate Chemical compound CCOCCOC(=O)OOC(=O)OCCOCC VGZZAZYCLRYTNQ-UHFFFAOYSA-N 0.000 description 1
- PCJJPMPLYYESTQ-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol 3-sulfanylpentanoic acid Chemical compound CCC(S)CC(O)=O.CCC(S)CC(O)=O.CCC(S)CC(O)=O.CCC(CO)(CO)CO PCJJPMPLYYESTQ-UHFFFAOYSA-N 0.000 description 1
- IIRMVAAETYZDSP-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol 4-sulfanylpentanoic acid Chemical compound CC(S)CCC(O)=O.CC(S)CCC(O)=O.CC(S)CCC(O)=O.CCC(CO)(CO)CO IIRMVAAETYZDSP-UHFFFAOYSA-N 0.000 description 1
- HFGWEGUVPBZOEA-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;2-methyl-2-sulfanylpropanoic acid Chemical compound CC(C)(S)C(O)=O.CC(C)(S)C(O)=O.CC(C)(S)C(O)=O.CCC(CO)(CO)CO HFGWEGUVPBZOEA-UHFFFAOYSA-N 0.000 description 1
- IYGAVZICZNAMTF-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;2-methyl-3-sulfanylpropanoic acid Chemical compound SCC(C)C(O)=O.SCC(C)C(O)=O.SCC(C)C(O)=O.CCC(CO)(CO)CO IYGAVZICZNAMTF-UHFFFAOYSA-N 0.000 description 1
- WBEKRAXYEBAHQF-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;3-sulfanylbutanoic acid Chemical compound CC(S)CC(O)=O.CC(S)CC(O)=O.CC(S)CC(O)=O.CCC(CO)(CO)CO WBEKRAXYEBAHQF-UHFFFAOYSA-N 0.000 description 1
- QPXVRLXJHPTCPW-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-(4-propan-2-ylphenyl)propan-1-one Chemical compound CC(C)C1=CC=C(C(=O)C(C)(C)O)C=C1 QPXVRLXJHPTCPW-UHFFFAOYSA-N 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- QKTWWGYCVXCKOJ-UHFFFAOYSA-N 2-methoxy-1-(2-methoxyphenyl)-2-phenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1OC QKTWWGYCVXCKOJ-UHFFFAOYSA-N 0.000 description 1
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 1
- RTEZVHMDMFEURJ-UHFFFAOYSA-N 2-methylpentan-2-yl 2,2-dimethylpropaneperoxoate Chemical compound CCCC(C)(C)OOC(=O)C(C)(C)C RTEZVHMDMFEURJ-UHFFFAOYSA-N 0.000 description 1
- PNLNUWORIZMRHX-UHFFFAOYSA-N 2-phenoxyethyl 3-sulfanylbutanoate Chemical compound SC(CC(=O)OCCOC1=CC=CC=C1)C PNLNUWORIZMRHX-UHFFFAOYSA-N 0.000 description 1
- KTALPKYXQZGAEG-UHFFFAOYSA-N 2-propan-2-ylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C(C)C)=CC=C3SC2=C1 KTALPKYXQZGAEG-UHFFFAOYSA-N 0.000 description 1
- KFGFVPMRLOQXNB-UHFFFAOYSA-N 3,5,5-trimethylhexanoyl 3,5,5-trimethylhexaneperoxoate Chemical compound CC(C)(C)CC(C)CC(=O)OOC(=O)CC(C)CC(C)(C)C KFGFVPMRLOQXNB-UHFFFAOYSA-N 0.000 description 1
- IFVYLGBXAXTHSC-UHFFFAOYSA-N 3-(3-sulfanylpropoxy)propane-1-thiol Chemical group SCCCOCCCS IFVYLGBXAXTHSC-UHFFFAOYSA-N 0.000 description 1
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 description 1
- ZBQGMMDOBGOEHH-UHFFFAOYSA-N 3-methyl-3-sulfanylbutanoic acid Chemical compound CC(C)(S)CC(O)=O ZBQGMMDOBGOEHH-UHFFFAOYSA-N 0.000 description 1
- FKPUSVBCWWJJEU-UHFFFAOYSA-N 4-(3-sulfanylbutoxy)butane-2-thiol Chemical group CC(S)CCOCCC(C)S FKPUSVBCWWJJEU-UHFFFAOYSA-N 0.000 description 1
- VWAMCRGFVJJNHC-UHFFFAOYSA-N 4-(4-sulfanylbutoxy)butane-1-thiol Chemical group SCCCCOCCCCS VWAMCRGFVJJNHC-UHFFFAOYSA-N 0.000 description 1
- UGVRJVHOJNYEHR-UHFFFAOYSA-N 4-chlorobenzophenone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1=CC=CC=C1 UGVRJVHOJNYEHR-UHFFFAOYSA-N 0.000 description 1
- OQEAEWQOPZQPSS-UHFFFAOYSA-N 4-isocyanatobutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCN=C=O OQEAEWQOPZQPSS-UHFFFAOYSA-N 0.000 description 1
- NFWPZNNZUCPLAX-UHFFFAOYSA-N 4-methoxy-3-methylaniline Chemical compound COC1=CC=C(N)C=C1C NFWPZNNZUCPLAX-UHFFFAOYSA-N 0.000 description 1
- KVKHEXRJTGZSOT-UHFFFAOYSA-N 6-(5-sulfanylhexoxy)hexane-2-thiol Chemical group CC(S)CCCCOCCCCC(C)S KVKHEXRJTGZSOT-UHFFFAOYSA-N 0.000 description 1
- YFEKCGCUBYDMAS-UHFFFAOYSA-N 7,7-dimethyl-2-(2,4,4-trimethylpentan-2-yl)octaneperoxoic acid Chemical compound CC(C)(C)CCCCC(C(=O)OO)C(C)(C)CC(C)(C)C YFEKCGCUBYDMAS-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- ZHLONWXGWNFBHY-UHFFFAOYSA-N C1(CCCCC1)C(C)(C)OOCCCCCCC(C)(C)C Chemical compound C1(CCCCC1)C(C)(C)OOCCCCCCC(C)(C)C ZHLONWXGWNFBHY-UHFFFAOYSA-N 0.000 description 1
- IGTDXGXYCNFEAT-UHFFFAOYSA-N CC(C)(CC(OCCCCOC(CC(C)(C)NC)=O)=O)NC Chemical compound CC(C)(CC(OCCCCOC(CC(C)(C)NC)=O)=O)NC IGTDXGXYCNFEAT-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- OQZFCEXSLBLEJN-UHFFFAOYSA-N [2-(isocyanatomethyl)-3-prop-2-enoyloxypropyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CN=C=O)COC(=O)C=C OQZFCEXSLBLEJN-UHFFFAOYSA-N 0.000 description 1
- OWENYJIXMBIZBB-UHFFFAOYSA-N [3-(2-methyl-2-sulfanylpropanoyl)oxy-2,2-bis[(2-methyl-2-sulfanylpropanoyl)oxymethyl]propyl] 2-methyl-2-sulfanylpropanoate Chemical compound CC(C)(S)C(=O)OCC(COC(=O)C(C)(C)S)(COC(=O)C(C)(C)S)COC(=O)C(C)(C)S OWENYJIXMBIZBB-UHFFFAOYSA-N 0.000 description 1
- UEUSKMPCQXJIGH-UHFFFAOYSA-N [3-(2-methyl-3-sulfanylpropanoyl)oxy-2,2-bis[(2-methyl-3-sulfanylpropanoyl)oxymethyl]propyl] 2-methyl-3-sulfanylpropanoate Chemical compound SCC(C)C(=O)OCC(COC(=O)C(C)CS)(COC(=O)C(C)CS)COC(=O)C(C)CS UEUSKMPCQXJIGH-UHFFFAOYSA-N 0.000 description 1
- VDKDFKRKAPXHBH-UHFFFAOYSA-N [3-(2-sulfanylpropanoyloxy)-2,2-bis(2-sulfanylpropanoyloxymethyl)propyl] 2-sulfanylpropanoate Chemical compound CC(S)C(=O)OCC(COC(=O)C(C)S)(COC(=O)C(C)S)COC(=O)C(C)S VDKDFKRKAPXHBH-UHFFFAOYSA-N 0.000 description 1
- MNYHVWARLWVWHX-UHFFFAOYSA-N [3-(3-phenyl-3-sulfanylpropanoyl)oxy-2,2-bis[(3-phenyl-3-sulfanylpropanoyl)oxymethyl]propyl] 3-phenyl-3-sulfanylpropanoate Chemical compound C=1C=CC=CC=1C(S)CC(=O)OCC(COC(=O)CC(S)C=1C=CC=CC=1)(COC(=O)CC(S)C=1C=CC=CC=1)COC(=O)CC(S)C1=CC=CC=C1 MNYHVWARLWVWHX-UHFFFAOYSA-N 0.000 description 1
- VTLHIRNKQSFSJS-UHFFFAOYSA-N [3-(3-sulfanylbutanoyloxy)-2,2-bis(3-sulfanylbutanoyloxymethyl)propyl] 3-sulfanylbutanoate Chemical compound CC(S)CC(=O)OCC(COC(=O)CC(C)S)(COC(=O)CC(C)S)COC(=O)CC(C)S VTLHIRNKQSFSJS-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- ZLSMCQSGRWNEGX-UHFFFAOYSA-N bis(4-aminophenyl)methanone Chemical compound C1=CC(N)=CC=C1C(=O)C1=CC=C(N)C=C1 ZLSMCQSGRWNEGX-UHFFFAOYSA-N 0.000 description 1
- RFVHVYKVRGKLNK-UHFFFAOYSA-N bis(4-methoxyphenyl)methanone Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=C(OC)C=C1 RFVHVYKVRGKLNK-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Chemical group 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- JMWLIBYMTSAPGR-UHFFFAOYSA-N decane-2,9-dithiol Chemical compound CC(S)CCCCCCC(C)S JMWLIBYMTSAPGR-UHFFFAOYSA-N 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 239000012933 diacyl peroxide Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- YLQWCDOCJODRMT-UHFFFAOYSA-N fluoren-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C2=C1 YLQWCDOCJODRMT-UHFFFAOYSA-N 0.000 description 1
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- MHLUCOKRQATVES-UHFFFAOYSA-N hexane-2,5-dithiol Chemical compound CC(S)CCC(C)S MHLUCOKRQATVES-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 150000004678 hydrides Chemical group 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- FSPSELPMWGWDRY-UHFFFAOYSA-N m-Methylacetophenone Chemical compound CC(=O)C1=CC=CC(C)=C1 FSPSELPMWGWDRY-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- RBQRWNWVPQDTJJ-UHFFFAOYSA-N methacryloyloxyethyl isocyanate Chemical compound CC(=C)C(=O)OCCN=C=O RBQRWNWVPQDTJJ-UHFFFAOYSA-N 0.000 description 1
- ZQMHJBXHRFJKOT-UHFFFAOYSA-N methyl 2-[(1-methoxy-2-methyl-1-oxopropan-2-yl)diazenyl]-2-methylpropanoate Chemical compound COC(=O)C(C)(C)N=NC(C)(C)C(=O)OC ZQMHJBXHRFJKOT-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
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
- XNTUJOTWIMFEQS-UHFFFAOYSA-N octadecanoyl octadecaneperoxoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCCCCCCCC XNTUJOTWIMFEQS-UHFFFAOYSA-N 0.000 description 1
- SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- YPVDWEHVCUBACK-UHFFFAOYSA-N propoxycarbonyloxy propyl carbonate Chemical compound CCCOC(=O)OOC(=O)OCCC YPVDWEHVCUBACK-UHFFFAOYSA-N 0.000 description 1
- UDEWPOVQBGFNGE-UHFFFAOYSA-N propyl benzoate Chemical compound CCCOC(=O)C1=CC=CC=C1 UDEWPOVQBGFNGE-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000007784 solid electrolyte Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- NMOALOSNPWTWRH-UHFFFAOYSA-N tert-butyl 7,7-dimethyloctaneperoxoate Chemical compound CC(C)(C)CCCCCC(=O)OOC(C)(C)C NMOALOSNPWTWRH-UHFFFAOYSA-N 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
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000001029 thermal curing Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 150000003553 thiiranes Chemical class 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 125000005628 tolylene group Chemical group 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 125000006839 xylylene group Chemical group 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/81—Unsaturated isocyanates or isothiocyanates
- C08G18/8108—Unsaturated isocyanates or isothiocyanates having only one isocyanate or isothiocyanate group
- C08G18/8116—Unsaturated isocyanates or isothiocyanates having only one isocyanate or isothiocyanate group esters of acrylic or alkylacrylic acid having only one isocyanate or isothiocyanate group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3855—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur
- C08G18/3876—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur containing mercapto groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/81—Unsaturated isocyanates or isothiocyanates
- C08G18/8141—Unsaturated isocyanates or isothiocyanates masked
- C08G18/815—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen
- C08G18/8158—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen
- C08G18/8175—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen with esters of acrylic or alkylacrylic acid having only one group containing active hydrogen
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C09J175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/0045—Photosensitive materials with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/0275—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with dithiol or polysulfide compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Optics & Photonics (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Epoxy Resins (AREA)
Description
このような硬化性組成物は、上記の光学材料や電子材料の各用途分野における高機能化の要求に従って、反応性、硬化特性、硬化物の透過率や屈折率などの光学特性、基材に対する密着性、耐熱性などの各性能の要求レベルも上がってきている。
この種の硬化性組成物は1液型あるいは2液型の光硬化タイプであり、光照射により、ポリエチレン性不飽和二重結合を含有する化合物とチオール化合物とがラジカル重合して数秒から数分の短時間で硬化する。しかし、このような従来のポリエン・ポリチオール系の光硬化性組成物は、加工性、硬化性に優れている反面、安定性が悪く、使用前に液体状態で保持しておくと増粘し、ゲル化を起こしやすい。また、そのような保持状態の組成物から作成した光硬化物は耐熱性が低いという問題点があった。
1. 一般式(1)
で示される基を2個以上含有するチオール化合物と、一般式(2)
で示されるエチレン性不飽和二重結合含有ウレタン化合物を含むことを特徴とする硬化性組成物。
2. 一般式(2)で示されるエチレン性不飽和二重結合含有ウレタン化合物のウレタン当量が、10〜40%である前記1に記載の硬化性組成物。
3. チオール化合物が、一般式(3)
で示されるメルカプト基含有カルボン酸と多官能アルコールとのエステル化合物である前記1に記載の硬化性組成物。
4. 前記1に記載のチオール化合物のR1およびR2が、少なくとも一方は炭素数1〜10のアルキル基を表わし、残りの基は水素原子を表わす前記1または2に記載の硬化性組成物。
5. 多官能アルコールが、分岐していてもよい炭素数2〜10のアルキレン基を持つアルキレングリコール、ジエチレングリコール、ジプロピレングリコール、グリセリン、トリメチロールプロパン、ペンタエリスリトールおよびジペンタエリスリトール、シクロヘキサンジオール、シクロヘキサンジメタノール、ノルボルネンジメタノール、2,2−ビス[4−(2−ヒドロキシエチルオキシ)フェニル]プロパン、水素化ビスフェノールA、4,4'−(9−フルオレニリデン)ビス(2−フェノキシエタノール)、およびトリス−2−ヒドロキシエチルイソシアヌレートから選ばれる化合物である前記3に記載の硬化性組成物。
6. チオール化合物が、一般式(4)
で示される化合物である前記3に記載の硬化性組成物。
7. チオール化合物が、一般式(5)
で示される化合物である前記3に記載の硬化性組成物。
8. チオール化合物が、式(6)
9. チオール化合物が、式(7)
10. チオール化合物が、式(8)
11. チオール化合物が、式(9)
12. チオール化合物が、式(10)
13. チオール化合物が、式(11)
14. エチレン性不飽和二重結合含有ウレタン化合物が、一般式(12)
で示される化合物である前記1または2に記載の硬化性組成物。
15. エチレン性不飽和二重結合含有ウレタン化合物が、一般式(13)
で示される化合物である前記1または2に記載の硬化性組成物。
16. エチレン性不飽和二重結合含有ウレタン化合物が、一般式(14)
で示される化合物である前記1または2に記載の硬化性組成物。
17. エチレン性不飽和二重結合含有ウレタン化合物が、一般式(15)
で示される化合物である前記1または2に記載の硬化性組成物。
18. チオール化合物とエチレン性不飽和二重結合含有ウレタン化合物に、さらに光重合開始剤を含む前記1〜17のいずれかに記載の硬化性組成物。
19. 前記1〜18のいずれかに記載の硬化性組成物によって得られる硬化物。
特に、得られる硬化反応性、硬化収縮の緩和、基材への密着性、透明性などの特徴から光学材料、コーティング材料、レジスト、UV硬化塗料などに適している。しかし、それらに限定されるものでない。
で示されるようなエステル構造、あるいは(c)一般式(17)
で示されるようなエーテル構造を含む化合物が挙げられ、中でも(b)または(c)の基を含む化合物が好ましい。また、保存性の観点からは、2級または3級チオール化合物を用いることが望ましい。
で示されるメルカプト基含有カルボン酸とアルコール類をエステル化することにより合成できる化合物が含まれる。この際、エステル化反応後の化合物を多官能チオール化合物とするために、アルコール類として多官能アルコールを用いる。
で示される多官能チオール化合物が好ましい。
本発明に使用されるエチレン性不飽和二重結合含有ウレタン化合物は、ラジカル重合(または架橋)反応および付加反応により硬化可能な化合物である。これらは1種または2種以上を組み合わせて用いることができる。
R4は酸素原子、硫黄原子またはイミノ基を表わし、R4としては酸素原子または硫黄原子が好ましい。
R5は単結合または炭素数1〜5の直鎖または分岐状のアルキレン基を表わす。R5としては、単結合、メチレン基、エチレン基等が挙げられ、中でも単結合が好ましい。
R6は水素原子またはメチル基を表わし、
R7は水素原子、炭素数1〜6の直鎖または分岐状のアルキル基およびアリール基からなる群から選ばれる少なくとも一種の基を表わす。R7としては、水素原子、メチル基、エチル基等のアルキル基、フェニル基、トリル基、ナフチル基等のアリール基が挙げられ、中でも水素原子、フェニル基が好ましい。
Xは脂肪族基、芳香族基、および複素環基から選ばれる一種の基を表わす。Xとしては、エチレングリコール、1,3−プロパンジオール、1,4−ブタンジオール、1,6−ヘキサンジオール、トリメチロールプロパン、ペンタエリスリトール、ノルボルネンジメタノール、ノルボルナンジメタノール、ポリカーボネートジオール、両末端ヒドロキシポリシリコーン、2,2−ビス[4−(2−ヒドロキシエチルオキシ)フェニル]プロパン、トリス(2−ヒドロキシエチル)イソシアヌレートなどのようなポリオールまたは2−ヒドロキシ(メタ)アクリレートのようなアルコール化合物の残基が挙げられ、中でも1,6−ヘキサンジオール、トリス(2−ヒドロキシエチル)イソシアヌレート、2,2−ビス[4−(2−ヒドロキシエチルオキシ)フェニル]プロパンまたは2−ヒドロキシ(メタ)アクリレートの残基が好ましい。
pは1〜3の整数を表わし、qは1〜4の整数を表わす。
で示される化合物、一般式(13)
で示される化合物、一般式(14)
で示される化合物、一般式(15)
で示される化合物等が挙げられる。
本発明の硬化性組成物は重合開始剤を添加してもよく、例えば、光あるいは熱重合開始剤が使用できる。本発明においては光重合開始剤が好ましい。
光重合開始剤は、紫外線あるいは可視光線、あるいは電子線などの活性エネルギー線を照射することで活性化し、樹脂成分がこれに反応することで連鎖的に重合反応および付加反応を起こし硬化物を得ることができる。
本発明の硬化性組成物は、以下のように配合、調整できる。
本発明で用いるチオール化合物とエチレン性不飽和二重結合含有ウレタン化合物、および必要に応じて重合開始剤を室温または加熱条件下で、ミキサー、ボールミルあるいは3本ロールなどの混合機により混合するか、あるいは、溶剤などを希釈剤として添加し溶解し、配合、調整することができる。
〔1〕硬化性組成物の調製および評価サンプルの作成
表1に記載されたチオール化合物(TH−1〜TH−13)、表2に記載されたエチレン性不飽和二重結合含有ウレタン化合物(モノマー化合物)(M−1〜M−12)および重合開始剤として1−ヒドロキシ−シクロヘキシル−フェニル−ケトン(チバスペシャルティケミカルズ社製,Irgacure184)をそれぞれ表3に記載の配合量とし、ジクロロメタン(純正化学社製)20gに室温で撹拌混合し、均一に溶解させて硬化性組成物溶液を得た。
さらに、これらの硬化性組成物溶液をガラス基板(大きさ50mm×50mm)上に、乾燥膜厚が約200μmとなるように塗布し、50℃で30分間溶剤を真空乾燥させ、実施例1〜24および比較例1〜6の評価サンプルを得た。
比較例に使用した表2中のエチレン性不飽和二重結合含有ウレタン化合物「M−11」および「M−12」は、以下の(メタ)アクリル基含有重合体である。
M−11:ブチルメタクリレートと2−ヒドロキシエチルアクリレートをmol比4:1の配合比で重合した共重合体を「P−1」(ポリスチレン換算数平均分子量(Mn)=14000、ポリスチレン換算重量平均分子量(Mw)=25000)とし、この「P−1」にペンダントされたヒドロキシル基を、2−メタクリロイルオキシエチルイソシアネートを用いてウレタン化したメタクリル基含有共重合体。すなわち表2中(A−1)および(A−2)の繰り返し単位を有する共重合体であり、繰り返し単位の構成比は4:1である。
M−12:前記「P−1」にペンダントされたヒドロキシル基を、2−アクリロイルオキシエチルイソシアネートを用いてウレタン化したアクリル基含有共重合体。すなわち表2中(A−1)および(A−3)の繰り返し単位を有する共重合体であり、繰り返し単位の構成比は4:1である。
前記分子量Mn、Mwは、GPC測定によりGPC導出分子量を求めた。測定は以下の方法で行なった。
測定機器:島津製作所社製,C-R7A plus クロマトパック、
プレカラム:昭和電工社製,SHODEX GPC KF-G、
カラム:昭和電工社製,SHODEX GPC KF-8025×1、
昭和電工社製,SHODEX GPC KF-802×1、
昭和電工社製,SHODEX GPC K-801×1、
カラム温度:40℃、
展開溶媒:THF、
流速:1mL/min。
(1)反応性の測定
前記〔1〕で作成した評価サンプルのエチレン性不飽和二重結合基の吸収ピ−クを赤外分光計(日本分光社製,FT/IR7000)で測定したところ、810cm−1であった。このサンプルを、超高圧水銀ランプを組み込んだ露光装置(ウシオ電機社製,マルチライトML−251A/B)で反応が定常状態となる露光量(500mj/cm2)で露光した。その時のエチレン性不飽和二重結合基の吸収ピ−クの変化量
前記〔1〕で作成した評価サンプルを、超高圧水銀ランプを組み込んだ露光装置にて、3j/cm2の露光量で露光した。その硬化した各サンプルの硬化膜表面をサンドペーパーで磨き、さらにアドヒージョンテスター(Elcometer Instrument.Std社製,elcometor)で密着強度を測定した。その結果を表3に示す。
前記〔1〕で作成した評価サンプルを超高圧水銀ランプを組み込んだ露光装置で、露光量3j/cm2にて露光した。硬化した各サンプルについて、分光光度計(日本分光製,3100)を用いて、500nmにおける透過率を測定した。その結果を表3に示す。
前記〔1〕で作成した評価サンプルを超高圧水銀ランプを組み込んだ露光装置で、3j/cm2の露光量で露光し、得られた硬化物を以下の条件で測定した。その結果を表3に示す。
測定器:鉛筆硬度計(上島製作所社製)、
負荷:1kg、
鉛筆:三菱鉛筆社製,鉛筆硬度測定用鉛筆、
判定:傷の有無は目視で判定し、ほとんど傷が付かない結果が出た中で最も硬い鉛筆の硬度を鉛筆硬度とした。
前記〔1〕で作成した評価サンプルを超高圧水銀ランプを組み込んだ露光装置で、3j/cm2の露光量で露光し、得られた硬化物をDSCにて測定した。その結果を表3に示す。測定条件は以下の通り。
測定器:リガク社製,Thermo plus DSC8230、
昇温開始温度:25℃、
昇温速度:毎分10℃。
Claims (18)
- 一般式(1)
で示される基を2個以上含有するチオール化合物と、一般式(2)
で示されるエチレン性不飽和二重結合含有ウレタン化合物を含み、
前記チオール化合物が一般式(3)
で示されるメルカプト基含有カルボン酸と多官能アルコールとのエステル化合物であることを特徴とする硬化性組成物。 - 一般式(2)で示されるエチレン性不飽和二重結合含有ウレタン化合物のウレタン当量が、10〜40%である請求項1に記載の硬化性組成物。
- 前記のR1およびR2が、少なくとも一方は炭素数1〜10のアルキル基を表わし、残りの基は水素原子を表わす請求項1または2に記載の硬化性組成物。
- 多官能アルコールが、分岐していてもよい炭素数2〜10のアルキレン基を持つアルキレングリコール、ジエチレングリコール、ジプロピレングリコール、グリセリン、トリメチロールプロパン、ペンタエリスリトールおよびジペンタエリスリトール、シクロヘキサンジオール、シクロヘキサンジメタノール、ノルボルネンジメタノール、2,2−ビス[4−(2−ヒドロキシエチルオキシ)フェニル]プロパン、水素化ビスフェノールA、4,4’−(9−フルオレニリデン)ビス(2−フェノキシエタノール)、およびトリス−2−ヒドロキシエチルイソシアヌレートから選ばれる化合物である請求項1に記載の硬化性組成物。
- チオール化合物とエチレン性不飽和二重結合含有ウレタン化合物に、さらに光重合開始剤を含む請求項1〜16のいずれかに記載の硬化性組成物。
- 請求項1〜17のいずれかに記載の硬化性組成物によって得られる硬化物。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007555996A JP5301164B2 (ja) | 2006-01-26 | 2007-01-25 | チオール化合物を含有する硬化性組成物 |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006017788 | 2006-01-26 | ||
JP2006017788 | 2006-01-26 | ||
PCT/JP2007/051168 WO2007086461A1 (ja) | 2006-01-26 | 2007-01-25 | チオール化合物を含有する硬化性組成物 |
JP2007555996A JP5301164B2 (ja) | 2006-01-26 | 2007-01-25 | チオール化合物を含有する硬化性組成物 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPWO2007086461A1 JPWO2007086461A1 (ja) | 2009-06-18 |
JP5301164B2 true JP5301164B2 (ja) | 2013-09-25 |
Family
ID=38309250
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2007555996A Active JP5301164B2 (ja) | 2006-01-26 | 2007-01-25 | チオール化合物を含有する硬化性組成物 |
Country Status (8)
Country | Link |
---|---|
US (1) | US7888399B2 (ja) |
EP (1) | EP1983017B1 (ja) |
JP (1) | JP5301164B2 (ja) |
KR (1) | KR101293084B1 (ja) |
CN (1) | CN101374886B (ja) |
AT (1) | ATE554126T1 (ja) |
TW (1) | TWI394768B (ja) |
WO (1) | WO2007086461A1 (ja) |
Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5004818B2 (ja) * | 2007-02-19 | 2012-08-22 | 三菱レイヨン株式会社 | 硬化性組成物及びその硬化物 |
CN101679635A (zh) * | 2007-07-13 | 2010-03-24 | 昭和电工株式会社 | 固化性组合物及其固化物 |
JP5121374B2 (ja) * | 2007-09-28 | 2013-01-16 | 三井化学株式会社 | 液晶シール剤、それを用いた液晶表示パネルの製造方法、および液晶表示パネル |
CN104851474A (zh) * | 2007-10-29 | 2015-08-19 | 日立化成株式会社 | 电路连接材料、连接结构体及其制造方法 |
EP2222740B1 (en) * | 2007-12-21 | 2017-10-11 | Rolic AG | Functionalized photoreactive compounds |
JP2010002569A (ja) * | 2008-06-19 | 2010-01-07 | Toppan Printing Co Ltd | 感光性着色組成物及びこれを用いたカラーフィルタ基板 |
JP2010024255A (ja) * | 2008-07-15 | 2010-02-04 | Nippon Synthetic Chem Ind Co Ltd:The | 活性エネルギー線硬化型樹脂組成物及びコーティング剤組成物 |
JP5405174B2 (ja) | 2009-03-30 | 2014-02-05 | 富士フイルム株式会社 | インク組成物 |
JP5677727B2 (ja) * | 2009-04-20 | 2015-02-25 | 株式会社ブリヂストン | チオール基含有接着性樹脂組成物 |
JP5489616B2 (ja) | 2009-09-28 | 2014-05-14 | 富士フイルム株式会社 | インク組成物及び印刷物成型体の製造方法 |
CN102107340B (zh) * | 2009-12-24 | 2015-10-21 | 汉高股份有限及两合公司 | 一种焊膏组合物、焊膏及一种助焊剂 |
JP5554114B2 (ja) | 2010-03-29 | 2014-07-23 | 富士フイルム株式会社 | 活性放射線硬化型インクジェット用インク組成物、印刷物、印刷物の製造方法、印刷物成形体、及び印刷物成形体の製造方法 |
JP5591745B2 (ja) | 2010-03-31 | 2014-09-17 | 富士フイルム株式会社 | 活性放射線硬化性インク組成物、インクジェット記録用インク組成物、並びに印刷物、および印刷物成形体の製造方法 |
JP5647533B2 (ja) * | 2010-06-07 | 2014-12-24 | 昭和電工株式会社 | 安定化されたポリエン−ポリチオール系硬化性樹脂組成物 |
EP2588448B1 (en) * | 2010-07-01 | 2017-10-18 | Samsung Electronics Co., Ltd. | Composition for light-emitting particle-polymer composite, light-emitting particle-polymer composite, and device including the light-emitting particle-polymer composite |
US9382470B2 (en) * | 2010-07-01 | 2016-07-05 | Samsung Electronics Co., Ltd. | Thiol containing compositions for preparing a composite, polymeric composites prepared therefrom, and articles including the same |
EP2522684A1 (en) * | 2011-05-12 | 2012-11-14 | Recticel | Method for functionalising a thermoset isocyanate-based polymeric solid material. |
WO2013080737A1 (ja) | 2011-11-29 | 2013-06-06 | 新田ゼラチン株式会社 | 光硬化性シーリング用材料、シーリング方法、シーリング材およびそれを用いる筐体 |
KR101575139B1 (ko) | 2011-12-09 | 2015-12-08 | 삼성전자주식회사 | 백라이트 유닛 및 이를 포함하는 액정 디스플레이 장치 |
JP6034210B2 (ja) * | 2013-02-07 | 2016-11-30 | 株式会社有沢製作所 | 基材処理用組成物、積層基材の製造方法、及び積層基材 |
JP5794248B2 (ja) * | 2013-03-15 | 2015-10-14 | 富士ゼロックス株式会社 | トナー、液体現像剤、現像剤、現像剤カートリッジ、プロセスカートリッジ、画像形成装置および画像形成方法 |
JP6460901B2 (ja) * | 2015-04-28 | 2019-01-30 | 富士フイルム株式会社 | 硬化性組成物、硬化膜、有機el表示装置、液晶表示装置、タッチパネル及びタッチパネル表示装置 |
JP6582774B2 (ja) * | 2015-09-10 | 2019-10-02 | 日油株式会社 | 剥離シート用硬化性樹脂組成物、これを用いた工程基材、及び基材を保護する方法 |
JP6699145B2 (ja) * | 2015-11-30 | 2020-05-27 | 味の素株式会社 | 光および熱硬化性樹脂組成物 |
CN108779191B (zh) | 2016-03-07 | 2021-06-22 | 昭和电工株式会社 | 活性能量射线固化性组合物及其固化物 |
JP6952686B2 (ja) * | 2016-05-20 | 2021-10-20 | 昭和電工株式会社 | 炭素繊維強化樹脂用組成物、炭素繊維強化樹脂組成物、硬化物 |
JP6235079B2 (ja) * | 2016-06-24 | 2017-11-22 | 株式会社有沢製作所 | 基材処理用組成物、積層基材の製造方法、及び積層基材 |
CN107641200B (zh) * | 2017-09-20 | 2020-12-15 | 杭州乐一新材料科技有限公司 | 一种用于3d打印的硫醇‐烯光固化树脂及其制备方法 |
KR101935031B1 (ko) * | 2017-12-28 | 2019-01-03 | 에스케이씨 주식회사 | 플라스틱 광학 렌즈용 폴리티올 조성물 |
CA3095462A1 (en) * | 2018-03-28 | 2019-10-03 | Benjamin Lund | Thiol-acrylate polymers, methods of synthesis thereof and use in additive manufacturing technologies |
CN113956477B (zh) * | 2020-07-20 | 2023-10-13 | 中国石油化工股份有限公司 | 一种固化组合物及其应用和固化聚合物材料及其制备方法和应用 |
CN112898565A (zh) * | 2021-03-09 | 2021-06-04 | 贵州大学 | 一种基于点击化学制备聚氨酯的方法及聚氨酯 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04266927A (ja) * | 1991-02-22 | 1992-09-22 | Mitsui Toatsu Chem Inc | 高硬度透明樹脂 |
JPH0593070A (ja) * | 1991-04-09 | 1993-04-16 | Showa Highpolymer Co Ltd | 外観の優れた成形品を形成可能な硬化性組成物 |
JPH10332901A (ja) * | 1997-06-02 | 1998-12-18 | Seed:Kk | 合成樹脂製レンズ |
JPH1121352A (ja) * | 1997-07-03 | 1999-01-26 | Toray Ind Inc | 硬化性組成物 |
JP2000206301A (ja) * | 1999-01-08 | 2000-07-28 | Hoya Corp | 光学材料およびそれを用いた光学製品 |
WO2003072614A2 (en) * | 2002-02-28 | 2003-09-04 | Showa Denko K.K. | Thiol compound, photopolymerization initiator composition and photosensitive composition |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4020233A (en) * | 1976-01-22 | 1977-04-26 | W. R. Grace & Co. | Heat activated ethylenically unsaturated-polythiol compositions |
US4785064A (en) * | 1984-07-10 | 1988-11-15 | Minnesota Mining And Manufacturing Company | Ultra-violet light curable compositions for abrasion resistant articles |
US5236967A (en) * | 1990-01-12 | 1993-08-17 | Asahi Denka Kogyo K.K. | Optical molding resin composition comprising polythiol-polyene compounds |
US5393607A (en) * | 1992-01-13 | 1995-02-28 | Mitsui Toatsu Chemiclas, Inc. | Laminated transparent plastic material and polymerizable monomer |
AUPP155998A0 (en) * | 1998-01-29 | 1998-02-19 | Sola International Holdings Ltd | Coating composition |
JP2001026608A (ja) | 1999-05-10 | 2001-01-30 | Denki Kagaku Kogyo Kk | 光硬化性樹脂組成物 |
JP4126918B2 (ja) | 2002-02-07 | 2008-07-30 | 三菱瓦斯化学株式会社 | 高屈折率光硬化性組成物およびその硬化物 |
JP4218828B2 (ja) | 2002-02-28 | 2009-02-04 | 昭和電工株式会社 | チオール化合物、光重合開始剤組成物および感光性組成物 |
JP4034098B2 (ja) | 2002-03-25 | 2008-01-16 | 電気化学工業株式会社 | ポリエン−ポリチオール系光硬化性樹脂組成物 |
JP2004264435A (ja) | 2003-02-28 | 2004-09-24 | Showa Denko Kk | カラーフィルタ用感光性組成物およびこれを用いたカラーフィルタ |
JP2005195977A (ja) | 2004-01-08 | 2005-07-21 | Sekisui Chem Co Ltd | 液晶表示素子用硬化性樹脂組成物、液晶表示素子用シール剤、上下導通材料、及び、液晶表示素子 |
JP3955038B2 (ja) | 2004-04-16 | 2007-08-08 | 積水化学工業株式会社 | 液晶表示素子用硬化性樹脂組成物 |
DE602005026430D1 (de) * | 2004-11-04 | 2011-03-31 | Showa Denko Kk | Isocyanatverbindung enthaltend eine ethylenisch ungesättigte gruppe und verfahren zu deren herstellung, sowie reaktives monomer, reaktives (meth)acrylatpolymer und anwendung davon |
JP3884758B2 (ja) * | 2005-03-11 | 2007-02-21 | 積水化学工業株式会社 | 塩基増殖剤及び塩基反応性硬化性組成物 |
-
2007
- 2007-01-25 CN CN2007800035367A patent/CN101374886B/zh active Active
- 2007-01-25 EP EP07713700A patent/EP1983017B1/en not_active Not-in-force
- 2007-01-25 KR KR1020087017623A patent/KR101293084B1/ko active IP Right Grant
- 2007-01-25 WO PCT/JP2007/051168 patent/WO2007086461A1/ja active Application Filing
- 2007-01-25 US US12/162,081 patent/US7888399B2/en not_active Expired - Fee Related
- 2007-01-25 AT AT07713700T patent/ATE554126T1/de active
- 2007-01-25 JP JP2007555996A patent/JP5301164B2/ja active Active
- 2007-01-26 TW TW096103036A patent/TWI394768B/zh active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04266927A (ja) * | 1991-02-22 | 1992-09-22 | Mitsui Toatsu Chem Inc | 高硬度透明樹脂 |
JPH0593070A (ja) * | 1991-04-09 | 1993-04-16 | Showa Highpolymer Co Ltd | 外観の優れた成形品を形成可能な硬化性組成物 |
JPH10332901A (ja) * | 1997-06-02 | 1998-12-18 | Seed:Kk | 合成樹脂製レンズ |
JPH1121352A (ja) * | 1997-07-03 | 1999-01-26 | Toray Ind Inc | 硬化性組成物 |
JP2000206301A (ja) * | 1999-01-08 | 2000-07-28 | Hoya Corp | 光学材料およびそれを用いた光学製品 |
WO2003072614A2 (en) * | 2002-02-28 | 2003-09-04 | Showa Denko K.K. | Thiol compound, photopolymerization initiator composition and photosensitive composition |
Also Published As
Publication number | Publication date |
---|---|
ATE554126T1 (de) | 2012-05-15 |
TWI394768B (zh) | 2013-05-01 |
US20090023831A1 (en) | 2009-01-22 |
US7888399B2 (en) | 2011-02-15 |
KR20080088603A (ko) | 2008-10-02 |
EP1983017B1 (en) | 2012-04-18 |
CN101374886B (zh) | 2011-08-10 |
TW200734364A (en) | 2007-09-16 |
CN101374886A (zh) | 2009-02-25 |
EP1983017A4 (en) | 2010-09-08 |
WO2007086461A1 (ja) | 2007-08-02 |
JPWO2007086461A1 (ja) | 2009-06-18 |
EP1983017A1 (en) | 2008-10-22 |
KR101293084B1 (ko) | 2013-08-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5301164B2 (ja) | チオール化合物を含有する硬化性組成物 | |
JP5126455B1 (ja) | ラジカル硬化性ホットメルトウレタン樹脂組成物、及び光学用成形体 | |
KR102369628B1 (ko) | 자외선 경화형 점착제 조성물, 자외선 경화형 점착 시트의 제조 방법, 및 적층체의 제조 방법 | |
CA2076504A1 (en) | Radiation curable composition with high temperature oil resistance | |
JP5822052B1 (ja) | 紫外線硬化型粘着剤組成物、粘着フィルム、及び、粘着フィルムの製造方法 | |
JP5641382B1 (ja) | 紫外線硬化型粘着剤組成物及び粘着剤 | |
JP2009503143A (ja) | 光学物品用硬化性チオール−エン組成物 | |
JP2007023147A (ja) | 光学材料用活性エネルギー線硬化型組成物 | |
KR101148521B1 (ko) | 중합 촉진제, 경화성 조성물, 경화물 및 티올 화합물의 제조 방법 | |
JPWO2019142601A1 (ja) | インプリント用光硬化性組成物 | |
JP6302894B2 (ja) | 多官能(メタ)アクリル酸エステル共重合体、硬化性樹脂組成物及びその硬化物 | |
JP5967461B1 (ja) | 紫外線硬化型粘着剤組成物、及び、粘着シート | |
JPWO2019167461A1 (ja) | ポリマーを含むインプリント用光硬化性組成物 | |
JP5741985B1 (ja) | 光硬化性樹脂組成物、その硬化物、及びプラスチックレンズ | |
JP2022128911A (ja) | 重合性組成物及びそれを重合硬化してなる樹脂 | |
JP6155927B2 (ja) | 紫外線硬化型粘着剤組成物、粘着剤及び粘着フィルム | |
JP2009098412A (ja) | カラーフィルタ用熱硬化性樹脂組成物およびカラーフィルタ | |
JP6593147B2 (ja) | 紫外線硬化型粘着剤組成物 | |
JP2002138131A (ja) | エポキシ(メタ)アクリレート及び該エポキシ(メタ)アクリレートを用いた樹脂組成物並びにこれらの硬化物 | |
WO1997000276A1 (en) | Active energy ray-curable resin compositions, a cured article and an optical lens obtained therefrom, and novel (meth)acrylate compounds therefor | |
JP4673281B2 (ja) | 活性エネルギー線硬化型非水性樹脂組成物、紫外線硬化型非水性樹脂組成物 | |
JP2001139645A (ja) | 注型光重合用樹脂組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20091023 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20091023 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20121113 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20121212 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20130618 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20130619 |
|
R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 Ref document number: 5301164 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313111 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
S531 | Written request for registration of change of domicile |
Free format text: JAPANESE INTERMEDIATE CODE: R313531 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |