JPH0160124B2 - - Google Patents
Info
- Publication number
- JPH0160124B2 JPH0160124B2 JP12623685A JP12623685A JPH0160124B2 JP H0160124 B2 JPH0160124 B2 JP H0160124B2 JP 12623685 A JP12623685 A JP 12623685A JP 12623685 A JP12623685 A JP 12623685A JP H0160124 B2 JPH0160124 B2 JP H0160124B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- weight
- parts
- acid
- itaconate
- 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.)
- Expired
Links
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 25
- -1 fluoroalkyl alcohol Chemical compound 0.000 claims description 24
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 20
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 19
- 150000002148 esters Chemical class 0.000 claims description 19
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 18
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 125000005375 organosiloxane group Chemical group 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 150000005846 sugar alcohols Polymers 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 125000001153 fluoro group Chemical group F* 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 238000007334 copolymerization reaction Methods 0.000 claims 1
- 239000000178 monomer Substances 0.000 description 16
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 230000035699 permeability Effects 0.000 description 6
- ZQTYRTSKQFQYPQ-UHFFFAOYSA-N trisiloxane Chemical compound [SiH3]O[SiH2]O[SiH3] ZQTYRTSKQFQYPQ-UHFFFAOYSA-N 0.000 description 6
- 150000005690 diesters Chemical class 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- WYGWHHGCAGTUCH-ISLYRVAYSA-N V-65 Substances CC(C)CC(C)(C#N)\N=N\C(C)(C#N)CC(C)C WYGWHHGCAGTUCH-ISLYRVAYSA-N 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- DDJSWKLBKSLAAZ-UHFFFAOYSA-N cyclotetrasiloxane Chemical compound O1[SiH2]O[SiH2]O[SiH2]O[SiH2]1 DDJSWKLBKSLAAZ-UHFFFAOYSA-N 0.000 description 3
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 239000000203 mixture Substances 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 239000002861 polymer material Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 229910000077 silane Inorganic materials 0.000 description 3
- QTKPMCIBUROOGY-UHFFFAOYSA-N 2,2,2-trifluoroethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(F)(F)F QTKPMCIBUROOGY-UHFFFAOYSA-N 0.000 description 2
- ZNJXRXXJPIFFAO-UHFFFAOYSA-N 2,2,3,3,4,4,5,5-octafluoropentyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(F)(F)C(F)(F)C(F)(F)C(F)F ZNJXRXXJPIFFAO-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
- LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 description 2
- WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 description 2
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 2
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 2
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 2
- HCLJOFJIQIJXHS-UHFFFAOYSA-N 2-[2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOCCOC(=O)C=C HCLJOFJIQIJXHS-UHFFFAOYSA-N 0.000 description 2
- LTHJXDSHSVNJKG-UHFFFAOYSA-N 2-[2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(C)=C LTHJXDSHSVNJKG-UHFFFAOYSA-N 0.000 description 2
- ZDYFQCBKPMLJGH-UHFFFAOYSA-N 2-[3-(2,4,4,6-tetramethyl-6,8,8-tripropyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocan-2-yl)propoxy]ethyl prop-2-enoate Chemical compound CCC[Si]1(C)O[Si](C)(C)O[Si](C)(CCCOCCOC(=O)C=C)O[Si](CCC)(CCC)O1 ZDYFQCBKPMLJGH-UHFFFAOYSA-N 0.000 description 2
- ZWKZTILIRRPWSK-UHFFFAOYSA-N 2-[3-[[dimethyl(trimethylsilyloxy)silyl]oxy-dimethylsilyl]propoxy]ethyl prop-2-enoate Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)CCCOCCOC(=O)C=C ZWKZTILIRRPWSK-UHFFFAOYSA-N 0.000 description 2
- VCEMDGWSPNMWJI-UHFFFAOYSA-N 2-[3-[dimethyl(trimethylsilyloxy)silyl]propoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCC[Si](C)(C)O[Si](C)(C)C VCEMDGWSPNMWJI-UHFFFAOYSA-N 0.000 description 2
- FQNKYQCIFNCQHT-UHFFFAOYSA-N 2-[3-tris(trimethylsilyloxy)silylpropoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](C)(C)C FQNKYQCIFNCQHT-UHFFFAOYSA-N 0.000 description 2
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- BCAJUCSKCNRGPJ-UHFFFAOYSA-N CC(=C)C(=O)OCCOCCC[Si](O[SiH2]C(O[Si](C)(C)C)O[Si](C)(C)C)(O[SiH2]C(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](CCCOCCOC(=O)C(=C)C)(O[SiH2]C(O[Si](C)(C)C)O[Si](C)(C)C)O[SiH2]C(O[Si](C)(C)C)O[Si](C)(C)C Chemical compound CC(=C)C(=O)OCCOCCC[Si](O[SiH2]C(O[Si](C)(C)C)O[Si](C)(C)C)(O[SiH2]C(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](CCCOCCOC(=O)C(=C)C)(O[SiH2]C(O[Si](C)(C)C)O[Si](C)(C)C)O[SiH2]C(O[Si](C)(C)C)O[Si](C)(C)C BCAJUCSKCNRGPJ-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- ZWWQRMFIZFPUAA-UHFFFAOYSA-N dimethyl 2-methylidenebutanedioate Chemical compound COC(=O)CC(=C)C(=O)OC ZWWQRMFIZFPUAA-UHFFFAOYSA-N 0.000 description 2
- UJKWLAZYSLJTKA-UHFFFAOYSA-N edma Chemical compound O1CCOC2=CC(CC(C)NC)=CC=C21 UJKWLAZYSLJTKA-UHFFFAOYSA-N 0.000 description 2
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 150000005691 triesters Chemical class 0.000 description 2
- FMQPBWHSNCRVQJ-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-yl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C(F)(F)F)C(F)(F)F FMQPBWHSNCRVQJ-UHFFFAOYSA-N 0.000 description 1
- MNSWITGNWZSAMC-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-yl prop-2-enoate Chemical compound FC(F)(F)C(C(F)(F)F)OC(=O)C=C MNSWITGNWZSAMC-UHFFFAOYSA-N 0.000 description 1
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
- VDYWHVQKENANGY-UHFFFAOYSA-N 1,3-Butyleneglycol dimethacrylate Chemical compound CC(=C)C(=O)OC(C)CCOC(=O)C(C)=C VDYWHVQKENANGY-UHFFFAOYSA-N 0.000 description 1
- NFPLJTNXOKFJRO-UHFFFAOYSA-N 1-ethenylpyridin-2-one Chemical compound C=CN1C=CC=CC1=O NFPLJTNXOKFJRO-UHFFFAOYSA-N 0.000 description 1
- VBHXIMACZBQHPX-UHFFFAOYSA-N 2,2,2-trifluoroethyl prop-2-enoate Chemical compound FC(F)(F)COC(=O)C=C VBHXIMACZBQHPX-UHFFFAOYSA-N 0.000 description 1
- CLISWDZSTWQFNX-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(F)(F)C(F)(F)F CLISWDZSTWQFNX-UHFFFAOYSA-N 0.000 description 1
- JDVGNKIUXZQTFD-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropyl prop-2-enoate Chemical compound FC(F)(F)C(F)(F)COC(=O)C=C JDVGNKIUXZQTFD-UHFFFAOYSA-N 0.000 description 1
- VIEHKBXCWMMOOU-UHFFFAOYSA-N 2,2,3,3,4,4,4-heptafluorobutyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(F)(F)C(F)(F)C(F)(F)F VIEHKBXCWMMOOU-UHFFFAOYSA-N 0.000 description 1
- PLXOUIVCSUBZIX-UHFFFAOYSA-N 2,2,3,3,4,4,4-heptafluorobutyl prop-2-enoate Chemical compound FC(F)(F)C(F)(F)C(F)(F)COC(=O)C=C PLXOUIVCSUBZIX-UHFFFAOYSA-N 0.000 description 1
- YSQGYEYXKXGAQA-UHFFFAOYSA-N 2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctyl prop-2-enoate Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)COC(=O)C=C YSQGYEYXKXGAQA-UHFFFAOYSA-N 0.000 description 1
- RSVZYSKAPMBSMY-UHFFFAOYSA-N 2,2,3,3-tetrafluoropropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(F)(F)C(F)F RSVZYSKAPMBSMY-UHFFFAOYSA-N 0.000 description 1
- VHJHZYSXJKREEE-UHFFFAOYSA-N 2,2,3,3-tetrafluoropropyl prop-2-enoate Chemical compound FC(F)C(F)(F)COC(=O)C=C VHJHZYSXJKREEE-UHFFFAOYSA-N 0.000 description 1
- OOHZIRUJZFRULE-UHFFFAOYSA-N 2,2-dimethylpropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)(C)C OOHZIRUJZFRULE-UHFFFAOYSA-N 0.000 description 1
- IJLJDZOLZATUFK-UHFFFAOYSA-N 2,2-dimethylpropyl prop-2-enoate Chemical compound CC(C)(C)COC(=O)C=C IJLJDZOLZATUFK-UHFFFAOYSA-N 0.000 description 1
- OLQFXOWPTQTLDP-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCO OLQFXOWPTQTLDP-UHFFFAOYSA-N 0.000 description 1
- RWXMAAYKJDQVTF-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl prop-2-enoate Chemical compound OCCOCCOC(=O)C=C RWXMAAYKJDQVTF-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- PFHOSZAOXCYAGJ-UHFFFAOYSA-N 2-[(2-cyano-4-methoxy-4-methylpentan-2-yl)diazenyl]-4-methoxy-2,4-dimethylpentanenitrile Chemical compound COC(C)(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)(C)OC PFHOSZAOXCYAGJ-UHFFFAOYSA-N 0.000 description 1
- MZGMQAMKOBOIDR-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCO MZGMQAMKOBOIDR-UHFFFAOYSA-N 0.000 description 1
- VETIYACESIPJSO-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound OCCOCCOCCOC(=O)C=C VETIYACESIPJSO-UHFFFAOYSA-N 0.000 description 1
- LOFVSJNCUNFRBZ-UHFFFAOYSA-N 2-[3-(2,4,4,6,6,8,8-heptamethyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocan-2-yl)propoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCC[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 LOFVSJNCUNFRBZ-UHFFFAOYSA-N 0.000 description 1
- DWBHKNHMULUVLM-UHFFFAOYSA-N 2-[3-(2,4,4,6,6,8,8-heptamethyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocan-2-yl)propoxy]ethyl prop-2-enoate Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(CCCOCCOC(=O)C=C)O[Si](C)(C)O1 DWBHKNHMULUVLM-UHFFFAOYSA-N 0.000 description 1
- KIDMRVDYDFQLRW-UHFFFAOYSA-N 2-[3-(2,4,4,6-tetramethyl-6,8,8-tripropyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocan-2-yl)propoxy]ethyl 2-methylprop-2-enoate Chemical compound CCC[Si]1(C)O[Si](C)(C)O[Si](C)(CCCOCCOC(=O)C(C)=C)O[Si](CCC)(CCC)O1 KIDMRVDYDFQLRW-UHFFFAOYSA-N 0.000 description 1
- JPZQHXPCLLMMEE-UHFFFAOYSA-N 2-[3-(methyl-phenyl-trimethylsilyloxysilyl)propoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCC[Si](C)(O[Si](C)(C)C)C1=CC=CC=C1 JPZQHXPCLLMMEE-UHFFFAOYSA-N 0.000 description 1
- QUFHGOPBRXWLPV-UHFFFAOYSA-N 2-[3-(methyl-phenyl-trimethylsilyloxysilyl)propoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCC[Si](C)(O[Si](C)(C)C)C1=CC=CC=C1 QUFHGOPBRXWLPV-UHFFFAOYSA-N 0.000 description 1
- IJBCHZAIEFCSJQ-UHFFFAOYSA-N 2-[3-[[[dimethyl(trimethylsilyloxy)silyl]oxy-dimethylsilyl]oxy-methyl-phenylsilyl]propoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCC[Si](C)(O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C)C1=CC=CC=C1 IJBCHZAIEFCSJQ-UHFFFAOYSA-N 0.000 description 1
- GJQPUDBTTKPFQR-UHFFFAOYSA-N 2-[3-[[dimethyl(trimethylsilyloxy)silyl]oxy-dimethylsilyl]propoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCC[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C GJQPUDBTTKPFQR-UHFFFAOYSA-N 0.000 description 1
- WJMZTAHWABUYEE-UHFFFAOYSA-N 2-[3-[[dimethyl(trimethylsilyloxy)silyl]oxy-dipropylsilyl]propoxy]ethyl 2-methylprop-2-enoate Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](CCC)(CCC)CCCOCCOC(=O)C(C)=C WJMZTAHWABUYEE-UHFFFAOYSA-N 0.000 description 1
- LDOQTSPCDHBTNE-UHFFFAOYSA-N 2-[3-[[dimethyl(trimethylsilyloxy)silyl]oxy-dipropylsilyl]propoxy]ethyl prop-2-enoate Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](CCC)(CCC)CCCOCCOC(=O)C=C LDOQTSPCDHBTNE-UHFFFAOYSA-N 0.000 description 1
- HWDSLOGOCOOOBI-UHFFFAOYSA-N 2-[3-[dimethyl(trimethylsilyloxy)silyl]propoxy]ethyl prop-2-enoate Chemical compound C[Si](C)(C)O[Si](C)(C)CCCOCCOC(=O)C=C HWDSLOGOCOOOBI-UHFFFAOYSA-N 0.000 description 1
- VZOFRWAWUHSXOR-UHFFFAOYSA-N 2-[3-[methyl-(2-methylpropyl)-trimethylsilyloxysilyl]propoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(C)C[Si](C)(O[Si](C)(C)C)CCCOCCOC(=O)C(C)=C VZOFRWAWUHSXOR-UHFFFAOYSA-N 0.000 description 1
- OCVBTGVFALKZLL-UHFFFAOYSA-N 2-[3-[methyl-(2-methylpropyl)-trimethylsilyloxysilyl]propoxy]ethyl prop-2-enoate Chemical compound CC(C)C[Si](C)(O[Si](C)(C)C)CCCOCCOC(=O)C=C OCVBTGVFALKZLL-UHFFFAOYSA-N 0.000 description 1
- HVNKAOZRKOCPDJ-UHFFFAOYSA-N 2-[3-[methyl-bis(trimethylsilyloxy)silyl]propoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C HVNKAOZRKOCPDJ-UHFFFAOYSA-N 0.000 description 1
- QCAKNOJNDONVPI-UHFFFAOYSA-N 2-[3-tris(trimethylsilyloxy)silylpropoxy]ethyl prop-2-enoate Chemical compound C[Si](C)(C)O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)CCCOCCOC(=O)C=C QCAKNOJNDONVPI-UHFFFAOYSA-N 0.000 description 1
- QKUVHYMCTPIYHI-UHFFFAOYSA-N 2-[3-tris[[cyclohexyl(dimethyl)silyl]oxy]silylpropoxy]ethyl 2-methylprop-2-enoate Chemical compound C1CCCCC1[Si](C)(C)O[Si](O[Si](C)(C)C1CCCCC1)(CCCOCCOC(=O)C(=C)C)O[Si](C)(C)C1CCCCC1 QKUVHYMCTPIYHI-UHFFFAOYSA-N 0.000 description 1
- YWNHLAAYWCFDCQ-UHFFFAOYSA-N 2-[3-tris[[cyclohexyl(dimethyl)silyl]oxy]silylpropoxy]ethyl prop-2-enoate Chemical compound C1CCCCC1[Si](C)(C)O[Si](CCCOCCOC(=O)C=C)(O[Si](C)(C)C1CCCCC1)O[Si](C)(C)C1CCCCC1 YWNHLAAYWCFDCQ-UHFFFAOYSA-N 0.000 description 1
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- WFGDTJSCHCKYOK-UHFFFAOYSA-N 3-(2-ethylhexoxycarbonyl)but-3-enoic acid Chemical compound CCCCC(CC)COC(=O)C(=C)CC(O)=O WFGDTJSCHCKYOK-UHFFFAOYSA-N 0.000 description 1
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- FQMIAEWUVYWVNB-UHFFFAOYSA-N 3-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OC(C)CCOC(=O)C=C FQMIAEWUVYWVNB-UHFFFAOYSA-N 0.000 description 1
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- VVAAYFMMXYRORI-UHFFFAOYSA-N 4-butoxy-2-methylidene-4-oxobutanoic acid Chemical compound CCCCOC(=O)CC(=C)C(O)=O VVAAYFMMXYRORI-UHFFFAOYSA-N 0.000 description 1
- RTTAGBVNSDJDTE-UHFFFAOYSA-N 4-ethoxy-2-methylidene-4-oxobutanoic acid Chemical compound CCOC(=O)CC(=C)C(O)=O RTTAGBVNSDJDTE-UHFFFAOYSA-N 0.000 description 1
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- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
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- SAPGBCWOQLHKKZ-UHFFFAOYSA-N 6-(2-methylprop-2-enoyloxy)hexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCOC(=O)C(C)=C SAPGBCWOQLHKKZ-UHFFFAOYSA-N 0.000 description 1
- OCIFJWVZZUDMRL-UHFFFAOYSA-N 6-hydroxyhexyl prop-2-enoate Chemical compound OCCCCCCOC(=O)C=C OCIFJWVZZUDMRL-UHFFFAOYSA-N 0.000 description 1
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- 101100424969 Arabidopsis thaliana TGD3 gene Proteins 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
- ICMSFQYICLGHOF-UHFFFAOYSA-N C(C(=C)C)(=O)OCCOCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)CCCCC Chemical compound C(C(=C)C)(=O)OCCOCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)CCCCC ICMSFQYICLGHOF-UHFFFAOYSA-N 0.000 description 1
- VWWRPIROJGBKPR-UHFFFAOYSA-N C(C(=C)C)(=O)OCCOCCC[Si](O[Si](CC1=CC=CC=C1)(CC1=CC=CC=C1)CC1=CC=CC=C1)(CC)CC Chemical compound C(C(=C)C)(=O)OCCOCCC[Si](O[Si](CC1=CC=CC=C1)(CC1=CC=CC=C1)CC1=CC=CC=C1)(CC)CC VWWRPIROJGBKPR-UHFFFAOYSA-N 0.000 description 1
- KXPNCSLALVCIIL-UHFFFAOYSA-N C(C(=C)C)(=O)OCCOCCC[Si](O[Si](CCC(=O)O)(C)C)(O[Si](CCC(=O)O)(C)C)O[Si](C)(C)CCC(=O)O Chemical compound C(C(=C)C)(=O)OCCOCCC[Si](O[Si](CCC(=O)O)(C)C)(O[Si](CCC(=O)O)(C)C)O[Si](C)(C)CCC(=O)O KXPNCSLALVCIIL-UHFFFAOYSA-N 0.000 description 1
- KOJIPWZZNAGREI-UHFFFAOYSA-N C(C=C)(=O)OCCOCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)CCCCC Chemical compound C(C=C)(=O)OCCOCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)CCCCC KOJIPWZZNAGREI-UHFFFAOYSA-N 0.000 description 1
- XGNAEHMQJQAFNE-UHFFFAOYSA-N C(C=C)(=O)OCCOCCC[Si](O[Si](CC1=CC=CC=C1)(CC1=CC=CC=C1)CC1=CC=CC=C1)(CC)CC Chemical compound C(C=C)(=O)OCCOCCC[Si](O[Si](CC1=CC=CC=C1)(CC1=CC=CC=C1)CC1=CC=CC=C1)(CC)CC XGNAEHMQJQAFNE-UHFFFAOYSA-N 0.000 description 1
- HHHFHOMKCQBZNM-UHFFFAOYSA-N CC(=C)C(=O)OCCOCCCC(CCCOCCOC(=O)C(=C)C)(CCCOCCOC(=O)C(=C)C)[SiH](C)O[SiH2]C Chemical compound CC(=C)C(=O)OCCOCCCC(CCCOCCOC(=O)C(=C)C)(CCCOCCOC(=O)C(=C)C)[SiH](C)O[SiH2]C HHHFHOMKCQBZNM-UHFFFAOYSA-N 0.000 description 1
- WHURLXPGXRAXOZ-UHFFFAOYSA-N CC(=C)C(=O)OCCOCCC[Si](O[Si](C)(C)CCOC(=O)C)(O[Si](C)(C)CCOC(=O)C)O[Si](CCCOCCOC(=O)C(=C)C)(O[Si](C)(C)CCOC(=O)C)O[Si](C)(C)CCOC(=O)C Chemical compound CC(=C)C(=O)OCCOCCC[Si](O[Si](C)(C)CCOC(=O)C)(O[Si](C)(C)CCOC(=O)C)O[Si](CCCOCCOC(=O)C(=C)C)(O[Si](C)(C)CCOC(=O)C)O[Si](C)(C)CCOC(=O)C WHURLXPGXRAXOZ-UHFFFAOYSA-N 0.000 description 1
- DOMKZGJOTCLGLJ-UHFFFAOYSA-N CC(OCCC[Si](C)(C)O[Si](C)(C)CCCOCCOC(=O)C)OC(=O)C(=C)C Chemical compound CC(OCCC[Si](C)(C)O[Si](C)(C)CCCOCCOC(=O)C)OC(=O)C(=C)C DOMKZGJOTCLGLJ-UHFFFAOYSA-N 0.000 description 1
- CYLIIGWAJTWRGO-UHFFFAOYSA-N C[SiH2]O[SiH](C)C(CCCOCCOC(=O)C=C)(CCCOCCOC(=O)C=C)CCCOCCOC(=O)C=C Chemical compound C[SiH2]O[SiH](C)C(CCCOCCOC(=O)C=C)(CCCOCCOC(=O)C=C)CCCOCCOC(=O)C=C CYLIIGWAJTWRGO-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 101000914502 Mus musculus CD2-associated protein Proteins 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- 239000007877 V-601 Substances 0.000 description 1
- ULQMPOIOSDXIGC-UHFFFAOYSA-N [2,2-dimethyl-3-(2-methylprop-2-enoyloxy)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)(C)COC(=O)C(C)=C ULQMPOIOSDXIGC-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- OICRDFIVTSEVJJ-UHFFFAOYSA-N bis(1,1,1,3,3,3-hexafluoropropan-2-yl) 2-methylidenebutanedioate Chemical compound FC(F)(F)C(C(F)(F)F)OC(=O)CC(=C)C(=O)OC(C(F)(F)F)C(F)(F)F OICRDFIVTSEVJJ-UHFFFAOYSA-N 0.000 description 1
- DTLYZSJVEDZWQX-UHFFFAOYSA-N bis(2,2-dimethylpropyl) 2-methylidenebutanedioate Chemical compound CC(C)(C)COC(=O)CC(=C)C(=O)OCC(C)(C)C DTLYZSJVEDZWQX-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- OGVXYCDTRMDYOG-UHFFFAOYSA-N dibutyl 2-methylidenebutanedioate Chemical compound CCCCOC(=O)CC(=C)C(=O)OCCCC OGVXYCDTRMDYOG-UHFFFAOYSA-N 0.000 description 1
- GFHMGSFDHKDJSG-UHFFFAOYSA-N dicyclohexyl 2-methylidenebutanedioate Chemical compound C1CCCCC1OC(=O)C(=C)CC(=O)OC1CCCCC1 GFHMGSFDHKDJSG-UHFFFAOYSA-N 0.000 description 1
- ZEFVHSWKYCYFFL-UHFFFAOYSA-N diethyl 2-methylidenebutanedioate Chemical compound CCOC(=O)CC(=C)C(=O)OCC ZEFVHSWKYCYFFL-UHFFFAOYSA-N 0.000 description 1
- MHAOABLQRSMPKK-UHFFFAOYSA-N dihexyl 2-methylidenebutanedioate Chemical compound CCCCCCOC(=O)CC(=C)C(=O)OCCCCCC MHAOABLQRSMPKK-UHFFFAOYSA-N 0.000 description 1
- NJCKCUVRQPTKTF-UHFFFAOYSA-N dipentyl 2-methylidenebutanedioate Chemical compound CCCCCOC(=O)CC(=C)C(=O)OCCCCC NJCKCUVRQPTKTF-UHFFFAOYSA-N 0.000 description 1
- IJBBERPAEBYDJT-UHFFFAOYSA-N dipropan-2-yl 2-methylidenebutanedioate Chemical compound CC(C)OC(=O)CC(=C)C(=O)OC(C)C IJBBERPAEBYDJT-UHFFFAOYSA-N 0.000 description 1
- DFQSWFGKYUFIFW-UHFFFAOYSA-N dipropyl 2-methylidenebutanedioate Chemical compound CCCOC(=O)CC(=C)C(=O)OCCC DFQSWFGKYUFIFW-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical compound C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 description 1
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 1
- GYDSPAVLTMAXHT-UHFFFAOYSA-N pentyl 2-methylprop-2-enoate Chemical compound CCCCCOC(=O)C(C)=C GYDSPAVLTMAXHT-UHFFFAOYSA-N 0.000 description 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- RGBXDEHYFWDBKD-UHFFFAOYSA-N propan-2-yl propan-2-yloxy carbonate Chemical compound CC(C)OOC(=O)OC(C)C RGBXDEHYFWDBKD-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- PQDJYEQOELDLCP-UHFFFAOYSA-N trimethylsilane Chemical compound C[SiH](C)C PQDJYEQOELDLCP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Eyeglasses (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12623685A JPS61285425A (ja) | 1985-06-12 | 1985-06-12 | コンタクトレンズ材料 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12623685A JPS61285425A (ja) | 1985-06-12 | 1985-06-12 | コンタクトレンズ材料 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61285425A JPS61285425A (ja) | 1986-12-16 |
JPH0160124B2 true JPH0160124B2 (de) | 1989-12-21 |
Family
ID=14930156
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12623685A Granted JPS61285425A (ja) | 1985-06-12 | 1985-06-12 | コンタクトレンズ材料 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61285425A (de) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4972037A (en) * | 1989-08-07 | 1990-11-20 | Minnesota Mining And Manufacturing Company | Polysiloxane-grafted copolymer topical binder composition with novel fluorochemical comonomer and method of coating therewith |
US5194556A (en) * | 1991-01-09 | 1993-03-16 | Ciba-Geigy Corporation | Rigid contact lenses with improved oxygen permeability |
US5208305A (en) * | 1992-04-17 | 1993-05-04 | Minnesota Mining And Manufacturing Company | Fluorine-containing polymers and preparation and use thereof |
WO2003027123A1 (fr) * | 2000-02-07 | 2003-04-03 | Johnson & Johnson Vision Care, Inc. | Monomeres, polymeres et lentilles ophtalmologiques |
JP5282532B2 (ja) * | 2008-11-07 | 2013-09-04 | 旭硝子株式会社 | 感光性樹脂組成物及びフォトレジスト |
EP2411431B1 (de) * | 2009-03-25 | 2014-10-01 | DSM IP Assets B.V. | Harzzusammensetzung |
CN102361933B (zh) * | 2009-03-25 | 2014-02-12 | 帝斯曼知识产权资产管理有限公司 | 乙烯基酯树脂组合物 |
CN109438494B (zh) * | 2018-11-22 | 2021-02-26 | 惠州瑞德新材料科技股份有限公司 | 一种可聚合反应性氟烃基硅氧烷改性丙烯酸酯的制备方法及应用 |
-
1985
- 1985-06-12 JP JP12623685A patent/JPS61285425A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS61285425A (ja) | 1986-12-16 |
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