JP4451137B2 - 配合可能な光開始剤 - Google Patents
配合可能な光開始剤 Download PDFInfo
- Publication number
- JP4451137B2 JP4451137B2 JP2003587844A JP2003587844A JP4451137B2 JP 4451137 B2 JP4451137 B2 JP 4451137B2 JP 2003587844 A JP2003587844 A JP 2003587844A JP 2003587844 A JP2003587844 A JP 2003587844A JP 4451137 B2 JP4451137 B2 JP 4451137B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- alkyl
- alkoxy
- acetate
- photoinitiator
- 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 - Lifetime
Links
- 239000000203 mixture Substances 0.000 claims abstract description 127
- 150000001875 compounds Chemical class 0.000 claims abstract description 99
- -1 -C(R5)-CR6R7 Chemical group 0.000 claims abstract description 95
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 35
- 239000001257 hydrogen Substances 0.000 claims abstract description 30
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 125000000466 oxiranyl group Chemical group 0.000 claims abstract description 8
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims abstract description 8
- 125000005569 butenylene group Chemical group 0.000 claims abstract description 5
- 125000005622 butynylene group Chemical group 0.000 claims abstract description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 3
- 125000004957 naphthylene group Chemical group 0.000 claims abstract description 3
- 238000000576 coating method Methods 0.000 claims description 68
- 238000004519 manufacturing process Methods 0.000 claims description 42
- 238000006243 chemical reaction Methods 0.000 claims description 40
- 238000000034 method Methods 0.000 claims description 36
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 26
- 239000000463 material Substances 0.000 claims description 26
- 238000002360 preparation method Methods 0.000 claims description 25
- 239000000654 additive Substances 0.000 claims description 24
- 239000000178 monomer Substances 0.000 claims description 24
- 229920000642 polymer Polymers 0.000 claims description 23
- 239000000976 ink Substances 0.000 claims description 21
- 238000007639 printing Methods 0.000 claims description 21
- 230000008569 process Effects 0.000 claims description 20
- 125000003545 alkoxy group Chemical group 0.000 claims description 18
- 125000002947 alkylene group Chemical group 0.000 claims description 17
- 239000000843 powder Substances 0.000 claims description 17
- 239000003054 catalyst Substances 0.000 claims description 16
- FAQJJMHZNSSFSM-UHFFFAOYSA-N phenylglyoxylic acid Chemical compound OC(=O)C(=O)C1=CC=CC=C1 FAQJJMHZNSSFSM-UHFFFAOYSA-N 0.000 claims description 16
- 239000000758 substrate Substances 0.000 claims description 16
- 239000002253 acid Substances 0.000 claims description 15
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 13
- 150000002148 esters Chemical class 0.000 claims description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 12
- 230000003287 optical effect Effects 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 239000003999 initiator Substances 0.000 claims description 10
- 229920001187 thermosetting polymer Polymers 0.000 claims description 9
- 239000008199 coating composition Substances 0.000 claims description 8
- 239000002131 composite material Substances 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- 239000012948 isocyanate Substances 0.000 claims description 8
- 238000007645 offset printing Methods 0.000 claims description 8
- 238000007650 screen-printing Methods 0.000 claims description 8
- 239000004305 biphenyl Substances 0.000 claims description 7
- 235000010290 biphenyl Nutrition 0.000 claims description 7
- 239000003365 glass fiber Substances 0.000 claims description 7
- 150000002513 isocyanates Chemical class 0.000 claims description 7
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 claims description 7
- 239000007858 starting material Substances 0.000 claims description 7
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 6
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 claims description 6
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims description 6
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 4
- 239000000292 calcium oxide Substances 0.000 claims description 4
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 4
- 125000004956 cyclohexylene group Chemical group 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 4
- 125000001624 naphthyl group Chemical group 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 claims description 3
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 3
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 claims description 3
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 3
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims description 3
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 claims description 3
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 claims description 3
- HDYRYUINDGQKMC-UHFFFAOYSA-M acetyloxyaluminum;dihydrate Chemical compound O.O.CC(=O)O[Al] HDYRYUINDGQKMC-UHFFFAOYSA-M 0.000 claims description 3
- 150000008065 acid anhydrides Chemical class 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 claims description 3
- 230000001070 adhesive effect Effects 0.000 claims description 3
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 claims description 3
- 229940009827 aluminum acetate Drugs 0.000 claims description 3
- ITHZDDVSAWDQPZ-UHFFFAOYSA-L barium acetate Chemical compound [Ba+2].CC([O-])=O.CC([O-])=O ITHZDDVSAWDQPZ-UHFFFAOYSA-L 0.000 claims description 3
- LHQLJMJLROMYRN-UHFFFAOYSA-L cadmium acetate Chemical compound [Cd+2].CC([O-])=O.CC([O-])=O LHQLJMJLROMYRN-UHFFFAOYSA-L 0.000 claims description 3
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 claims description 3
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 claims description 3
- 238000002845 discoloration Methods 0.000 claims description 3
- 238000005538 encapsulation Methods 0.000 claims description 3
- NONOKGVFTBWRLD-UHFFFAOYSA-N isocyanatosulfanylimino(oxo)methane Chemical compound O=C=NSN=C=O NONOKGVFTBWRLD-UHFFFAOYSA-N 0.000 claims description 3
- JILPJDVXYVTZDQ-UHFFFAOYSA-N lithium methoxide Chemical compound [Li+].[O-]C JILPJDVXYVTZDQ-UHFFFAOYSA-N 0.000 claims description 3
- LZWQNOHZMQIFBX-UHFFFAOYSA-N lithium;2-methylpropan-2-olate Chemical compound [Li+].CC(C)(C)[O-] LZWQNOHZMQIFBX-UHFFFAOYSA-N 0.000 claims description 3
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 claims description 3
- 239000011654 magnesium acetate Substances 0.000 claims description 3
- 235000011285 magnesium acetate Nutrition 0.000 claims description 3
- 229940069446 magnesium acetate Drugs 0.000 claims description 3
- 239000003094 microcapsule Substances 0.000 claims description 3
- 235000011056 potassium acetate Nutrition 0.000 claims description 3
- 239000001632 sodium acetate Substances 0.000 claims description 3
- 235000017281 sodium acetate Nutrition 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 238000012360 testing method Methods 0.000 claims description 3
- 239000004246 zinc acetate Substances 0.000 claims description 3
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 2
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 2
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
- 125000001064 morpholinomethyl group Chemical group [H]C([H])(*)N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 claims description 2
- 125000001422 pyrrolinyl group Chemical group 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 claims description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 238000004061 bleaching Methods 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 230000033458 reproduction Effects 0.000 claims 1
- 238000009472 formulation Methods 0.000 abstract description 28
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 54
- 239000011248 coating agent Substances 0.000 description 39
- 239000000049 pigment Substances 0.000 description 39
- 239000010410 layer Substances 0.000 description 27
- 239000002904 solvent Substances 0.000 description 20
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- 229910052757 nitrogen Inorganic materials 0.000 description 18
- 230000005855 radiation Effects 0.000 description 18
- 229920001577 copolymer Polymers 0.000 description 17
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 17
- 238000001723 curing Methods 0.000 description 16
- 239000000047 product Substances 0.000 description 16
- 229920005989 resin Polymers 0.000 description 15
- 239000011347 resin Substances 0.000 description 15
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- 239000000835 fiber Substances 0.000 description 12
- 239000013307 optical fiber Substances 0.000 description 12
- 239000003973 paint Substances 0.000 description 12
- 229920005862 polyol Polymers 0.000 description 12
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 150000001412 amines Chemical class 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 9
- 239000011230 binding agent Substances 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 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 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 8
- 150000002009 diols Chemical class 0.000 description 8
- 238000001035 drying Methods 0.000 description 8
- 229920002120 photoresistant polymer Polymers 0.000 description 8
- 229920000728 polyester Polymers 0.000 description 8
- 150000003077 polyols Chemical class 0.000 description 8
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 8
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 7
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 7
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 7
- 238000004821 distillation Methods 0.000 description 7
- 239000002609 medium Substances 0.000 description 7
- 229910052753 mercury Inorganic materials 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- 239000000600 sorbitol Substances 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical group CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
- 239000006096 absorbing agent Substances 0.000 description 6
- 229910052786 argon Inorganic materials 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 6
- 239000007859 condensation product Substances 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 6
- 239000004033 plastic Substances 0.000 description 6
- 229920000647 polyepoxide Polymers 0.000 description 6
- 229920000570 polyether Polymers 0.000 description 6
- 229920001296 polysiloxane Polymers 0.000 description 6
- 239000004814 polyurethane Substances 0.000 description 6
- 229920002635 polyurethane Polymers 0.000 description 6
- 150000003254 radicals Chemical class 0.000 description 6
- 239000002023 wood Substances 0.000 description 6
- 0 **OC(C(c1ccccc1)=O)=O Chemical compound **OC(C(c1ccccc1)=O)=O 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- DZRLZBYMIRXJGO-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxy]ethanol Chemical compound OCCOCCOCC1CO1 DZRLZBYMIRXJGO-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 5
- 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 5
- 150000004056 anthraquinones Chemical class 0.000 description 5
- 239000012965 benzophenone Substances 0.000 description 5
- 238000006555 catalytic reaction Methods 0.000 description 5
- 239000003086 colorant Substances 0.000 description 5
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 5
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 5
- 125000005442 diisocyanate group Chemical group 0.000 description 5
- 239000003085 diluting agent Substances 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 238000000921 elemental analysis Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 238000002329 infrared spectrum Methods 0.000 description 5
- 239000004611 light stabiliser Substances 0.000 description 5
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 239000000123 paper Substances 0.000 description 5
- 238000000016 photochemical curing Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000004408 titanium dioxide Substances 0.000 description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
- PQDJYEQOELDLCP-UHFFFAOYSA-N trimethylsilane Chemical compound C[SiH](C)C PQDJYEQOELDLCP-UHFFFAOYSA-N 0.000 description 5
- RQGSZGCFMVGVJR-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl 2-oxo-2-phenylacetate Chemical compound OCCOCCOC(=O)C(=O)C1=CC=CC=C1 RQGSZGCFMVGVJR-UHFFFAOYSA-N 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- 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 4
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- 239000004065 semiconductor Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- MNWBNISUBARLIT-UHFFFAOYSA-N sodium cyanide Chemical compound [Na+].N#[C-] MNWBNISUBARLIT-UHFFFAOYSA-N 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 150000005622 tetraalkylammonium hydroxides Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 150000004654 triazenes Chemical class 0.000 description 1
- KKFOMYPMTJLQGA-UHFFFAOYSA-N tribenzyl phosphite Chemical compound C=1C=CC=CC=1COP(OCC=1C=CC=CC=1)OCC1=CC=CC=C1 KKFOMYPMTJLQGA-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
- C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
-
- 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
- G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
- G03F7/031—Organic compounds not covered by group G03F7/029
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymerisation Methods In General (AREA)
- Epoxy Compounds (AREA)
- Holo Graphy (AREA)
- Pens And Brushes (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Liquid Crystal Substances (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Description
Yは、C3−C12アルキレン、ブテニレン、ブチニレン、又は−O−若しくは−NR2−により1回以上非連続的に中断されているC4−C12アルキレンであるか;あるいはYは、フェニレン、シクロヘキシレン、下記式:
R1は、OH、SH、NR3R4、−(CO)−OH、−(CO)−NH2、SO3H、−C(R5)=CR6R7、オキシラニル、−O−(CO)−NH−R8−NCO及び−O−(CO)−R9−(CO)−Xから選択される反応性基であり;
R2は、水素、C1−C4アルキル又はC2−C4ヒドロキシアルキルであり;
R3及びR4は、それぞれ他と独立に、水素、C1−C4アルキル又はC2−C4ヒドロキシアルキルであり;
R5、R6及びR7は、それぞれ他と独立に、水素又はメチルであり;
R8は、直鎖又は分岐のC4−C12アルキレン、フェニレン、メチル−フェニレン、シクロヘキサンジイル、イソホロンジイル、下記式:
R9は、直鎖又は分岐のC1−C16アルキレン、−CH=CH−、−CH=CH−CH2−、C6−シクロアルキレン、フェニレン、ナフチレン、ノルボルネン−5,6−ジイル、下記式:
X、X1及びX2は、それぞれ他と独立に、OH、Cl、OCH3又はOC2H5である]で示される配合可能な光開始剤化合物に関する。
Yが、−O−により1回以上非連続的に中断されているC4−C12アルキレンであり;
R1が、OH、オキシラニル及び−O−(CO)−NH−R8−NCOから選択される反応性基であり;そして
R8が、下記式:
で示されるフェニルグリオキシル酸モノエステルと、式(III):
HO−Y−OH (III)
[式中、Yは、上記と同義である]
で示されるジオールとの反応
[ここで、触媒として、酢酸リチウム、酢酸ナトリウム、酢酸カリウム、酢酸マグネシウム、酢酸バリウム、酢酸亜鉛、酢酸カドミウム、酢酸銅(II)、酢酸コバルト(II)、酢酸アルミニウム、酸化カルシウム、リチウムメタノラート、ナトリウムメタノラート、チタンテトライソプロパノラート、アルミニウムトリイソプロパノラート、リチウムtert−ブタノラート、4−(ジメチルアミノ)ピリジン又は二酢酸ジブチルスズが使用される]
による方法に関する。
(a)少なくとも1つのエチレン不飽和光重合性化合物と
(b)光開始剤として、少なくとも1つの式(I)の化合物と、
を含むことを特徴とする光重合性組成物に関するものであり、この組成物は、成分(b)に加えて、他の光開始剤(c)及び/又は他の添加剤(d)も含むことができる。
トリアクリル酸トリメチロールプロパン、トリアクリル酸トリメチロールエタン、トリメタクリル酸トリメチロールプロパン、トリメタクリル酸トリメチロールエタン、ジメタクリル酸テトラメチレングリコール、ジメタクリル酸トリエチレングリコール、ジアクリル酸テトラエチレングリコール、ジアクリル酸ペンタエリスリトール、トリアクリル酸ペンタエリスリトール、テトラアクリル酸ペンタエリスリトール、ジアクリル酸ジペンタエリスリトール、トリアクリル酸ジペンタエリスリトール、テトラアクリル酸ジペンタエリスリトール、ペンタアクリル酸ジペンタエリスリトール、ヘキサアクリル酸ジペンタエリスリトール、オクタアクリル酸トリペンタエリスリトール、ジメタクリル酸ペンタエリスリトール、トリメタクリル酸ペンタエリスリトール、ジメタクリル酸ジペンタエリスリトール、テトラメタクリル酸ジペンタエリスリトール、オクタメタクリル酸トリペンタエリスリトール、ジイタコン酸ペンタエリスリトール、トリスイタコン酸ジペンタエリスリトール、ペンタイタコン酸ジペンタエリスリトール、ヘキサイタコン酸ジペンタエリスリトール、ジアクリル酸エチレングリコール、ジアクリル酸1,3−ブタンジオール、ジメタクリル酸1,3−ブタンジオール、ジイタコン酸1,4−ブタンジオール、トリアクリル酸ソルビトール、テトラアクリル酸ソルビトール、変性トリアクリル酸ペンタエリスリトール、テトラメタクリル酸ソルビトール、ペンタアクリル酸ソルビトール、ヘキサアクリル酸ソルビトール、オリゴエステルアクリレート類及びメタクリレート類、ジ−及びトリ−アクリル酸グリセロール、ジアクリル酸1,4−シクロヘキサン、200〜1500の分子量を有するポリエチレングリコールのビスアクリレート類及びビスメタクリレート類、並びにこれらの混合物。
1. 2−(2’−ヒドロキシフェニル)ベンゾトリアゾール、例えば、2−(2’−ヒドロキシ−5’−メチルフェニル)−ベンゾトリアゾール、2−(3’,5’−ジ−tert−ブチル−2’−ヒドロキシフェニル)−ベンゾトリアゾール、2−(5’−tert−ブチル−2’−ヒドロキシフェニル)−ベンゾトリアゾール、2−(2’−ヒドロキシ−5’−(1,1,3,3−テトラメチルブチル)−フェニル)−ベンゾトリアゾール、2−(3’,5’−ジ−tert−ブチル−2’−ヒドロキシフェニル)−5−クロロベンゾトリアゾール、2−(3’−tert−ブチル−2’−ヒドロキシ−5’−メチルフェニル)−5−クロロベンゾトリアゾール、2−(3’−sec−ブチル−5’−tert−ブチル−2’−ヒドロキシフェニル)−ベンゾトリアゾール、2−(2’−ヒドロキシ−4’−オクチルオキシフェニル)−ベンゾトリアゾール、2−(3’,5’−ジ−tert−アミル−2’−ヒドロキシフェニル)−ベンゾトリアゾール、2−(3’,5’−ビス(α,α−ジメチルベンジル)−2’−ヒドロキシフェニル)−ベンゾトリアゾール;2−(3’−tert−ブチル−2’−ヒドロキシ−5’−(2−オクチルオキシカルボニルエチル)−フェニル)−5−クロロベンゾトリアゾール、2−(3’−tert−ブチル−5’−[2−(2−エチルヘキシルオキシ)−カルボニルエチル]−2’−ヒドロキシフェニル)−5−クロロベンゾトリアゾール、2−(3’−tert−ブチル−2’−ヒドロキシ−5’−(2−メトキシカルボニルエチル)−フェニル)−5−クロロベンゾトリアゾール、2−(3’−tert−ブチル−2’−ヒドロキシ−5’−(2−メトキシカルボニルエチル)フェニル)−ベンゾトリアゾール、2−(3’−tert−ブチル−2’−ヒドロキシ−5’−(2−オクチルオキシカルボニルエチル)フェニル)−ベンゾトリアゾール、2−(3’−tert−ブチル−5’−[2−(2−エチルヘキシルオキシ)−カルボニルエチル]−2’−ヒドロキシフェニル)−ベンゾトリアゾール、2−(3’−ドデシル−2’−ヒドロキシ−5’−メチルフェニル)−ベンゾトリアゾール及び2−(3’−tert−ブチル−2’−ヒドロキシ−5’−(2−イソオクチルオキシカルボニルエチル)−フェニル)−ベンゾトリアゾールの混合物;2,2’−メチレン−ビス[4−(1,1,3,3−テトラメチルブチル)−6−ベンゾトリアゾール−2−イル−フェノール];2−[3’−tert−ブチル−5’−(2−メトキシカルボニルエチル)−2’−ヒドロキシフェニル]−ベンゾトリアゾールとポリエチレングリコール300とのエステル交換生成物;[R−CH2CH2−COO(CH2)3]2−(ここで、R=3’−tert−ブチル−4’−ヒドロキシ−5’−2H−ベンゾトリアゾール−2−イル−フェニル)。
1. チオキサントン
チオキサントン、2−イソプロピルチオキサントン、3−イソプロピルチオキサントン、2−クロロチオキサントン、2−ドデシルチオキサントン、1−クロロ−4−プロポキシチオキサントン、2,4−ジエチルチオキサントン、2,4−ジメチルチオキサントン、1−メトキシカルボニルチオキサントン、2−エトキシカルボニルチオキサントン、3−(2−メトキシエトキシカルボニル)−チオキサントン、4−ブトキシカルボニルチオキサントン、3−ブトキシカルボニル−7−メチルチオキサントン、1−シアノ−3−クロロチオキサントン、1−エトキシカルボニル−3−クロロチオキサントン、1−エトキシカルボニル−3−エトキシチオキサントン、1−エトキシカルボニル−3−アミノチオキサントン、1−エトキシカルボニル−3−フェニルスルフリルチオキサントン、3,4−ジ[2−(2−メトキシエトキシ)エトキシカルボニル]チオキサントン、1−エトキシカルボニル−3−(1−メチル−1−モルホリノエチル)−チオキサントン、2−メチル−6−ジメトキシメチル−チオキサントン、2−メチル−6−(1,1−ジメトキシベンジル)−チオキサントン、2−モルホリノメチルチオキサントン、2−メチル−6−モルホリノメチルチオキサントン、N−アリルチオキサントン−3,4−ジカルボキシミド、N−オクチルチオキサントン−3,4−ジカルボキシミド、N−(1,1,3,3−テトラメチルブチル)−チオキサントン−3,4−ジカルボキシミド、1−フェノキシチオキサントン、6−エトキシカルボニル−2−メトキシチオキサントン、6−エトキシカルボニル−2−メチルチオキサントン、チオキサントン−2−ポリエチレングリコールエステル、2−ヒドロキシ−3−(3,4−ジメチル−9−オキソ−9H−チオキサントン−2−イルオキシ)−N,N,N−トリメチル−1−プロパンアミニウムクロリド;
ベンゾフェノン、4−フェニルベンゾフェノン、4−メトキシベンゾフェノン、4,4’−ジメトキシベンゾフェノン、4,4’−ジメチルベンゾフェノン、4,4’−ジクロロベンゾフェノン、4,4’−ジメチルアミノ−ベンゾフェノン、4,4’−ジエチルアミノベンゾフェノン、4−メチルベンゾフェノン、3−メチル−4’−フェニルベンゾフェノン、2,4,6−トリメチルベンゾフェノン、2,4,6−トリメチル−4’−フェニルベンゾフェノン、4−(4−メチルチオフェニル)−ベンゾフェノン、3,3’−ジメチル−4−メトキシベンゾフェノン、2−ベンゾイル安息香酸メチル、4−(2−ヒドロキシエチルチオ)−ベンゾフェノン、4−(4−トリルチオ)ベンゾフェノン、4−ベンゾイル−N,N,N−トリメチルベンゼンメタンアミニウムクロリド、2−ヒドロキシ−3−(4−ベンゾイルフェノキシ)−N,N,N−トリメチル−1−プロパンアミニウムクロリド一水和物、4−(13−アクリロイル−1,4,7,10,13−ペンタオキサトリデシル)−ベンゾフェノン、4−ベンゾイル−N,N−ジメチル−N−[2−(1−オキソ−2−プロペニル)オキシ]エチル−ベンゼンメタンアミニウムクロリド;
3−ベンゾイルクマリン、3−ベンゾイル−7−メトキシクマリン、3−ベンゾイル−5,7−ジ(プロポキシ)クマリン、3−ベンゾイル−6,8−ジクロロクマリン、3−ベンゾイル−6−クロロクマリン、3,3’−カルボニル−ビス[5,7−ジ(プロポキシ)クマリン]、3,3’−カルボニル−ビス(7−メトキシクマリン)、3,3’−カルボニル−ビス(7−ジエチルアミノ−クマリン)、3−イソブチロイルクマリン、3−ベンゾイル−5,7−ジメトキシクマリン、3−ベンゾイル−5,7−ジエトキシクマリン、3−ベンゾイル−5,7−ジブトキシクマリン、3−ベンゾイル−5,7−ジ(メトキシエトキシ)−クマリン、3−ベンゾイル−5,7−ジ(アリルオキシ)クマリン、3−ベンゾイル−7−ジメチルアミノクマリン、3−ベンゾイル−7−ジエチルアミノクマリン、3−イソブチロイル−7−ジメチルアミノクマリン、5,7−ジメトキシ−3−(1−ナフトイル)−クマリン、5,7−ジメトキシ−3−(1−ナフトイル)−クマリン、3−ベンゾイルベンゾ[f]クマリン、7−ジエチルアミノ−3−チエノイルクマリン、3−(4−シアノベンゾイル)−5,7−ジメトキシクマリン;
3−メチル−2−ベンゾイルメチレン−β−ナフトチアゾリン、3−メチル−2−ベンゾイルメチレン−ベンゾチアゾリン、3−エチル−2−プロピオニルメチレン−β−ナフトチアゾリン;
アセトフェノン、3−メトキシアセトフェノン、4−フェニルアセトフェノン、ベンジル、2−アセチルナフタレン、2−ナフトアルデヒド、9,10−アントラキノン、9−フルオレノン、ジベンゾスベロン、キサントン、2,5−ビス(4−ジエチルアミノベンジリデン)シクロペンタノン;2−(4−ジメチルアミノベンジリデン)−インダン−1−オン又は3−(4−ジメチルアミノ−フェニル)−1−インダン−5−イル−プロペノンのようなα−(パラ−ジメチルアミノベンジリデン)−ケトン;3−フェニルチオフタルイミド、N−メチル−3,5−ジ(エチルチオ)フタルイミド。
R25は、水素、C1−C18アルキル、C1−C18アルコキシ、−OCH2CH2−OR29、モルホリノ、SCH3又は下記式:
nは、2〜10であり;
G1及びG2は、それぞれ他と独立にポリマー単位の末端基、特に水素又はCH3であり;
R26は、ヒドロキシ、C1−C16アルコキシ、モルホリノ、ジメチルアミノ又は−O(CH2CH2O)m−C1−C16アルキルであり;
R27及びR28は、それぞれ他と独立に、水素、C1−C6アルキル、フェニル、ベンジル、アリル、C1−C16アルコキシ又は−O(CH2CH2O)m−C1−C16アルキルであるか、あるいはR27及びR28は、これらが結合している炭素原子と一緒になって、シクロヘキシル環を形成し;
mは、1〜20の数であり;ここで
R26、R27及びR28は、全てが同時にC1−C16アルコキシ又は−O(CH2CH2O)m−C1−C16アルキルであることはなく;そして
R29は、水素、下記式:
R30及びR32は、それぞれ他と独立に、水素又はメチルであり;
R31は、水素、メチル、2−ヒドロキシエチルチオ又はフェニルチオ(フェニルチオ基のフェニル環は、非置換であるか、又はC1−C4アルキルにより4−、2−、2,4−若しくは2,4,6−位で置換されている)であり;
R33及びR34は、それぞれ他と独立に、C1−C20アルキル、シクロヘキシル、シクロペンチル、フェニル、ナフチル又はビフェニルである(これらの基は、非置換であるか、又はハロゲン、C1−C12アルキル若しくは/及びC1−C12アルコキシにより置換されている)か、あるいはR33は、S−若しくはN−含有の5員若しくは6員複素環又は下記式:
R35は、シクロヘキシル、シクロペンチル、フェニル、ナフチル又はビフェニルである(これらの基は、非置換であるか、又は1つ以上のハロゲン、C1−C4アルキル若しくは/及びC1−C4アルコキシ置換基により置換されている)か、あるいはR35は、S−又はN−含有の5員又は6員複素環であり;
R36及びR37は、それぞれ他と独立に、非置換であるか、又はC1−C18アルキル、C1−C18アルコキシ、シクロペンチル、シクロヘキシル若しくはハロゲンによりモノ−、ジ−、若しくはトリ−置換されている、シクロペンタジエニルであり;そして
R38及びR39は、それぞれ他と独立に、チタン−炭素結合に対してオルトの2つの位置のうちの少なくとも1つでフッ素原子又はCF3により置換されており、かつ芳香環の更に別の置換基として、ピロリニル又はポリオキサアルキル(これらはそれぞれ、非置換であるか、又は1つ若しくは2つのC1−C12アルキル、ジ(C1−C12アルキル)アミノメチル、モルホリノメチル、C2−C4アルケニル、メトキシメチル、エトキシメチル、トリメチルシリル、ホルミル、メトキシ若しくはフェニル基により置換されている)を含んでいてもよい、フェニルであるか、あるいはR38及びR39は、下記式:
R40、R41及びR42は、それぞれ他と独立に、水素、ハロゲン、C2−C12アルケニル、C1−C12アルコキシ、1〜4個の酸素原子により中断されているC2−C12アルコキシ、シクロヘキシルオキシ、シクロペンチルオキシ、フェノキシ、ベンジルオキシ、非置換であるか、又はC1−C4アルコキシ−、ハロ−、フェニルチオ−若しくはC1−C4アルキルチオ−置換の、フェニル又はビフェニルであり;ここで、
R40及びR42は、両方が同時に水素であることはなく、かつ下記式:
E1は、O、S又はNR43であり;
R43は、C1−C8アルキル、フェニル又はシクロヘキシルであり;そして
Y1は、C3−C12アルキレン、ブテニレン、ブチニレン、又は−O−若しくは−NR44−により1回以上非連続的に中断されているC4−C12アルキレンであるか、あるいはY1は、フェニレン、シクロヘキシレン、下記式:
R44は、水素、C1−C4アルキル又はC2−C4ヒドロキシアルキルである]で示される化合物である組成物に関する。
R25が、水素、−OCH2CH2−OR29、モルホリノ、SCH3又は下記式:
R26が、ヒドロキシ、C1−C16アルコキシ、モルホリノ又はジメチルアミノであり;
R27及びR28が、それぞれ他と独立に、C1−C4アルキル、アリル、フェニル、ベンジル又はC1−C16アルコキシであるか、あるいはR27及びR28が、これらが結合している炭素原子と一緒に、シクロヘキシル環を形成し;
R29が、水素又は下記式:
R30、R31及びR32が、水素であり;
R33が、C1−C12アルキル、非置換フェニル、又はC1−C12アルキル若しくは/及びC1−C12アルコキシにより置換されているフェニルであり;
R34が、下記式:
R35が、1つ以上のC1−C4アルキル又は/及びC1−C4アルコキシ置換基により置換されているフェニルである組成物である。
下記式:
フェニルグリオキシル酸メチルエステル137.9g、ジエチレングリコール891.7g及び酢酸リチウム二水和物2.2gを初回充填として室温で、蒸留装置を取り付けた1.5リットル多口フラスコに入れた。撹拌しながら、8〜10mbarまで反応容器からゆっくり排気した。次に反応混合物を50〜60℃に加熱した。約72時間後、生成した全てのメタノールを蒸留により除去して、反応を終了させた。反応混合物を、水500mlと一緒に分液ロートに注ぎ入れ、トルエン100mlで3回抽出し、次にジエチルエーテル500mlで5回抽出した。エーテル相を合わせて、硫酸ナトリウムで乾燥して濾過した。溶媒を留去(ロータリーエバポレーターを用いる)後に生成物を得た。構造及び組成は、NMR分光法及びHPLC(高圧液体クロマトグラフィー)により確認した。
アルゴンガス下、トルエン15g中の、実施例1からのフェニルグリオキシル酸(2−ヒドロキシエトキシ)エチルエステル4.28g及び5−イソシアナト−1−イソシアナトメチル−1,1,3−トリメチルシクロヘキサン(ジイソシアン酸イソホロン、フルカ(Fluka))3.99gを初回充填として、50ml多口フラスコに入れて、110℃で還流した。18時間後、この溶液を冷却して、ロータリーエバポレーターを用いてトルエンを濃縮した。残渣を高真空下で2時間乾燥した。粘性の帯黄色の油状物8.2gを得た。生成物の変換率及び組成は、1H−NMRスペクトル及びIRスペクトル(NCOバンド)により検証した。
元素分析:C24H32N2O7 %C %H %N
[計算値/実測値] 62.59/63.55 7.00/7.07 6.08/6.07
アルゴンガス下、トルエン15g中の、実施例1からのフェニルグリオキシル酸(2−ヒドロキシエトキシ)エチルエステル2.14g及びジイソシアン酸4,4’−ジフェニルメタン(デスモジュール(Desmodur)VL、バイエル(Bayer))2.24gを初回充填として、50ml多口フラスコに入れて、110℃で還流した。19時間後、この溶液を冷却して、ロータリーエバポレーターを用いてトルエンを濃縮した。残渣を高真空下で2時間乾燥した。粘性のわずかに帯褐色の油状物4.6gを得た。生成混合物の変換率及び組成は、1H−NMRスペクトル及びIRスペクトル(NCOバンド)により検証した。
元素分析:C27H24N2O7 %C %H %N
[計算値/実測値] 66.39/67.54 4.95/5.19 5.73/5.52
アルゴンガス下、トルエン15g中の、実施例1からのフェニルグリオキシル酸(2−ヒドロキシエトキシ)エチルエステル2.14g及び1,3,5−トリス(6−イソシアナトヘキシル)−[1,3,5]トリアジナン−2,4,6−トリオン(デスモジュールN3300、バイエル)3.02gを初回充填として、50ml多口フラスコに入れて、110℃で還流した。16時間後、この溶液を冷却して、ロータリーエバポレーターを用いてトルエンを濃縮した。残渣を高真空下で3時間乾燥した。粘性の無色の油状物5.3gを得た。生成混合物の変換率及び組成は、1H−NMRスペクトル及びIRスペクトル(NCOバンド)により検証した。光開始剤に関しては、モノ生成物とビス生成物は、等比率で存在する。
元素分析:C48H64N6O16及びC36H50N6O11
%C %H %N
[計算値/実測値] 58.53/58.42 6.67/6.71 9.75/9.18
アルゴンガス下、トルエン15g中の、実施例1からのフェニルグリオキシル酸(2−ヒドロキシエトキシ)エチルエステル2.14g及び1,3,5−トリス(6−イソシアナトヘキシル)ビウレット(デスモジュールN3200、バイエル)2.86gを初回充填として、50ml多口フラスコに入れて、110℃で還流した。19時間後、この溶液を冷却して、ロータリーエバポレーターを用いてトルエンを濃縮した。残渣を高真空下で乾燥した。粘性の無色の油状物4.8gを得た。生成混合物の変換率及び組成は、1H−NMRスペクトル及びIRスペクトル(NCOバンド)により検証した。光開始剤に関しては、モノ生成物とビス生成物は、等比率で存在する。
元素分析:C47H66N6O15及びC35H52N6O10
%C %H %N
[計算値/実測値] 58.91/59.22 7.11/7.14 10.05/9.67
アルゴンガス下、トルエン15g中の、実施例1からのフェニルグリオキシル酸(2−ヒドロキシエトキシ)エチルエステル2.14g及び1,3−ビス(6−イソシアナトヘキシル)−[1,3]ジアゼチジン−2,4−ジオン(デスモジュールN3400、バイエル)3.02gを初回充填として、50ml多口フラスコに入れて、110℃で還流した。19時間後、この溶液を冷却して、ロータリーエバポレーターを用いてトルエンを濃縮した。残渣を高真空下で乾燥した。非常に粘性の無色の油状物5.2gを得た。生成混合物の変換率及び組成は、1H−NMRスペクトル及びIRスペクトル(NCOバンド)により検証した。
元素分析:C28H38N4O9
%C %H %N
[計算値/実測値] 58.53/58.57 6.67/6.95 9.75/9.63
7.1: 下記式:
窒素雰囲気下、ジエチレングリコール26.53g、過塩素酸ランタン六水和物0.25g及びトルエン50mlを初回充填として、集中冷却器とプロペラスターラーを取り付けた350mlスルホン化フラスコに入れて105℃に加熱した。105℃の内部温度に達した後、温度を一定に保持しながらエピクロロヒドリン21.3gを、70分間のうちに滴下により加えた。続いて105℃で14時間の撹拌後、トルエン30mlを反応混合物に加えることによって、次に未だ存在するあらゆる水を共沸蒸留により除去した。常圧で共沸混合物約30mlを留去した。48〜50℃に冷却後、ジアゾビシクロウンデセン約19gを、30分間のうちに滴下により加え、そして次にこの混合物を2時間撹拌した。室温まで冷却後、二相反応混合物の下相を、酢酸を用いてpH5〜8に調整し、塩化メチレンで希釈して食塩水各回約100mlで3回抽出した。硫酸マグネシウムで乾燥後、こうして得られた粗生成物を濃縮乾固して、わずかに帯黄色の粘性油状物27.1g(理論値の73%)を得た。粗生成物12gを、フラッシュクロマトグラフィー(シリカゲル60F 800g;酢酸エチル95:メタノール5)を用いて精製した。目的生成物は、純度約85%(GCにより測定)のわずかに帯黄色の油状物の形で得た。1H−NMRスペクトルによると、副産物(15%、GCにより測定)は、下記式:
フェニルグリオキシル酸メチルエステル217mg、実施例7.1により得られたジエチレングリコールモノグリシジルエーテル195mg及び酢酸リチウム10mgを初回充填として、ナスフラスコに入れた。このフラスコを、ロータリーエバポレーター中で60℃の浴温及び150mbarの減圧下で回転させた。2時間後、浴温を70℃に上昇させ、圧力を100mbarまで下げた。更に2時間後、反応溶液を、ヘキサン:酢酸エチル、1:1を用いてシリカゲル60Fのクロマトグラフィーに付した。わずかに帯黄色の油状物の形で標題化合物を得た。
以下の成分を混合することにより、光硬化性配合物を調製した:
89.0部 エポキシアクリレート(ジアクリル酸ヘキサンジオール中80%;エベクリル(Ebecryl)(登録商標)604)
10.0部 ポリエチレングリコール400ジアクリレート(サルトマー(Sartomer)(登録商標)SR344)
1.0部 流動性向上剤(エベクリル(登録商標)350)
実施例9〜14のために以下の配合物を調製した:
− 成分A
11.38部 ヒドロキシル基含有ポリアクリレート、酢酸ブチル中70%(デスモフェン(Desmophen)A870、バイエル(Bayer AG))
21.23部 ポリエステルポリオール、酢酸ブチル中75%(デスモフェンVP LS2089;バイエル)
0.55部 流動性向上剤(バイク(Byk)306;バイク化学(Byk Chemie))
32.03部 メタノール
− 成分B(使用した量は表1に与えられる)
イソシアナート基含有ウレタンアクリレート(ロスキダル(Roskydal)UA VP LS2337、バイエル)
Claims (13)
- 式(I):
Yは、C3−C12アルキレン、ブテニレン、ブチニレン、又は−O−若しくは−NR2−により1回以上非連続的に中断されているC4−C12アルキレンであるか;あるいはYは、フェニレン、シクロヘキシレン、下記式:
R1は、OH、SH、NR3R4、−(CO)−OH、−(CO)−NH2、SO3H、−C(R5)=CR6R7、オキシラニル、−O−(CO)−NH−R8−NCO及び−O−(CO)−R9−(CO)−Xから選択される反応性基であり;
R2は、水素、C1−C4アルキル又はC2−C4ヒドロキシアルキルであり;
R3及びR4は、それぞれ他と独立に、水素、C1−C4アルキル又はC2−C4ヒドロキシアルキルであり;
R5、R6及びR7は、それぞれ他と独立に、水素又はメチルであり;
R8は、直鎖又は分岐のC4−C12アルキレン、フェニレン、メチル−フェニレン、シクロヘキサンジイル、イソホロンジイル、下記式:
R9は、直鎖又は分岐のC1−C16アルキレン、−CH=CH−、−CH=CH−CH2−、C6−シクロアルキレン、フェニレン、ナフチレン、ノルボルネン−5,6−ジイル、下記式:
X、X1及びX2は、それぞれ他と独立に、OH、Cl、OCH3又はOC2H5である]で示される配合可能な光開始剤化合物。 - R1がOHである、請求項1記載の式(I)の化合物の製造方法であって、式(II):
- R1が、SH、NR3R4、−(CO)−OH、−(CO)−NH2、SO3H、−C(R5)=CR6R7、オキシラニル、−O−(CO)−NH−R8−NCO又は−O−(CO)−R9−(CO)−Xであり、そしてR3、R4、R5、R6、R7、R8、R9及びX基が、請求項1と同義である、配合可能な光開始剤の製造における出発物質としての、R1がOHである請求項1記載の式(I)の化合物の使用。
- R1がOHである請求項1記載の式(I)の化合物を、イソシアナート、塩化カルバモイル、チオイソシアナート、酸塩化物、酸エステル、酸無水物、クロロホルマート又はエピクロロヒドリンと反応させる、請求項1記載の式(I)の配合可能な光開始剤の製造方法。
- (a)少なくとも1つのエチレン不飽和光重合性化合物と、
(b)光開始剤として、少なくとも1つの請求項1記載の式(I)の化合物と、
を含むことを特徴とする、光重合性組成物。 - 成分(b)に加えて、更に別の開始剤(c)及び/又は添加剤(d)も含むことを特徴とする、請求項6記載の組成物。
- 追加の光開始剤(c)が、式(VIII)、(IX)、(X)、(XI)又は/及び(XII):
R25は、水素、C1−C18アルキル、C1−C18アルコキシ、−OCH2CH2−OR29、モルホリノ、SCH3、又は下記式:
nは、2〜10であり;
G1及びG2は、それぞれ他と独立に、ポリマー単位の末端基、特に水素又はCH3であり;
R26は、ヒドロキシ、C1−C16アルコキシ、モルホリノ、ジメチルアミノ又は−O(CH2CH2O)m−C1−C16アルキルであり;
R27及びR28は、それぞれ他と独立に、水素、C1−C6アルキル、フェニル、ベンジル、アリル、C1−C16アルコキシ又は−O(CH2CH2O)m−C1−C16アルキルであるか、あるいはR27及びR28は、これらが結合している炭素原子と一緒に、シクロヘキシル環を形成し;
mは、1〜20の数であり;ここで
R26、R27及びR28は、全てが同時にC1−C16アルコキシ又は−O(CH2CH2)m−C1−C16アルキルではなく、そして
R29は、水素、下記式:
R30及びR32は、それぞれ他と独立に、水素又はメチルであり;
R31は、水素、メチル、2−ヒドロキシエチルチオ又はフェニルチオ(フェニルチオ基のフェニル環は、非置換であるか、又はC1−C4アルキルにより4−、2−、2,4−若しくは2,4,6−位で置換されている)であり;
R33及びR34は、それぞれ他と独立に、C1−C20アルキル、シクロヘキシル、シクロペンチル、フェニル、ナフチル又はビフェニルであり、これらの基は、非置換であるか、又はハロゲン、C1−C12アルキル若しくは/及びC1−C12アルコキシにより置換されているか、あるいはR33は、S−若しくはN−含有の5員若しくは6員複素環又は下記式:
R35は、シクロヘキシル、シクロペンチル、フェニル、ナフチル又はビフェニルであり、これらの基は、非置換であるか、又は1つ以上のハロゲン、C1−C4アルキル若しくは/及びC1−C4アルコキシ置換基により置換されているか、あるいはR35は、S−又はN−含有の5員又は6員複素環であり;
R36及びR37は、それぞれ他と独立に、非置換であるか、又はC1−C18アルキル、C1−C18アルコキシ、シクロペンチル、シクロヘキシル若しくはハロゲンにより、モノ−、ジ−若しくはトリ−置換されている、シクロペンタジエニルであり;そして
R38及びR39は、それぞれ他と独立に、チタン炭素結合に対してオルトな2つの位置の少なくとも1つでフッ素原子又はCF3により置換されており、かつ芳香環上の更なる置換基として、ピロリニル又はポリオキサアルキル(これらはそれぞれ、非置換であるか、又は1つ若しくは2つのC1−C12アルキル、ジ(C1−C12アルキル)アミノメチル、モルホリノメチル、C2−C4アルケニル、メトキシメチル、エトキシメチル、トリメチルシリル、ホルミル、メトキシ若しくはフェニル基により置換されている)を含んでいてもよい、フェニルであるか、あるいはR38及びR39は、下記式:
R40、R41及びR42は、それぞれ他と独立に、水素、ハロゲン、C2−C12アルケニル、C1−C12アルコキシ、1〜4個の酸素原子により中断されているC2−C12アルコキシ、シクロヘキシルオキシ、シクロペンチルオキシ、フェノキシ、ベンジルオキシ、非置換又はC1−C4アルコキシ−、ハロ−、フェニルチオ−若しくはC1−C4アルキルチオ−置換の、フェニル又はビフェニルであり;ここで
R40及びR42は、両方同時に水素ではなく、かつ下記式:
E1は、O、S又はNR43であり;
R43は、C1−C8アルキル、フェニル又はシクロヘキシルであり;そして
Y1は、C3−C12アルキレン、ブテニレン、ブチニレン、又は−O−若しくは−NR44−により1回以上非連続的に中断されているC4−C12アルキレンであるか、あるいはY1は、フェニレン、シクロヘキシレン、下記式:
R44は、水素、C1−C4アルキル又はC2−C4ヒドロキシアルキルである]で示される化合物である、請求項7記載の組成物。 - 0.05〜20重量%の光開始剤成分(b)、又は0.05〜20重量%の光開始剤成分(b)+(c)を含む、請求項6〜8のいずれか1項記載の組成物。
- 光化学硬化性成分を含むことに加えて、熱硬化性成分も含む、請求項6記載の組成物。
- 200〜600nmの波長範囲の光での照射による、少なくとも1つのエチレン不飽和二重結合を有する不揮発性モノマー、オリゴマー又はポリマー化合物の光重合における光開始剤としての、請求項1記載の式(I)の化合物。
- 着色及び非着色表面コーティング組成物、印刷インキ、スクリーン印刷インキ、オフセット印刷インキ、フレキソ印刷インキ、粉体塗料、印刷版、接着剤、歯科用組成物、光導波管、光学スイッチ、変色試験系、複合材料、グラスファイバケーブル被覆、スクリーン印刷ステンシル、レジスト材料、カラーフィルター、ゲルコートの製造における;電気及び電子部品の封入における;磁気記録材料の製造における;立体リソグラフィーによる三次元物品、写真複製物、画像記録材料の製造における;脱色材料の製造における;又はマイクロカプセルを用いる画像記録材料の製造における、請求項6記載の組成物。
- 少なくとも1つの表面が、請求項6記載の組成物で被覆されている被覆基体。
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Families Citing this family (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7642296B2 (en) | 2004-04-19 | 2010-01-05 | Ciba Specialty Chemicals Corporation | Photoinitiators |
FR2871898B1 (fr) * | 2004-06-18 | 2006-09-08 | Alcatel Sa | Composant a fibre optique et fibre optique associee |
EP1836002B1 (en) * | 2004-12-22 | 2012-08-29 | Basf Se | Process for the production of strongly adherent coatings |
US20070012208A1 (en) * | 2005-07-13 | 2007-01-18 | Byungwoo Cho | Offset printing system |
EP2069866A2 (en) * | 2006-10-03 | 2009-06-17 | Ciba Holding Inc. | Photocurable compositions |
JP5196194B2 (ja) * | 2007-05-30 | 2013-05-15 | 日産化学工業株式会社 | ゲート絶縁膜とその形成剤、製造方法及びそれを用いる薄膜トランジスタ並びにその製造方法 |
ITVA20070073A1 (it) * | 2007-09-17 | 2009-03-18 | Lamberti Spa | Fotoiniziatori per reticolazione indotta dalla luce |
CN101583908B (zh) * | 2007-11-20 | 2012-12-26 | 日立化成工业株式会社 | 感光性树脂组合物、感光性树脂固化物、感光性树脂膜、感光性树脂膜固化物和使用它们得到的光波导 |
JP5192277B2 (ja) * | 2008-04-14 | 2013-05-08 | シャープ株式会社 | 固体撮像装置の製造方法 |
US7970247B2 (en) * | 2008-09-12 | 2011-06-28 | Draka Comteq B.V. | Buffer tubes for mid-span storage |
US8401353B2 (en) * | 2008-09-12 | 2013-03-19 | Draka Comteq B.V. | Optical fiber cable assembly |
RU2465888C1 (ru) * | 2008-11-11 | 2012-11-10 | Колгейт-Палмолив Компани | Композиция с красящим веществом для указания степени покрытия |
WO2010077132A1 (en) | 2008-12-31 | 2010-07-08 | Draka Comteq B.V. | Uvled apparatus for curing glass-fiber coatings |
DE102009001966A1 (de) | 2009-03-30 | 2010-10-07 | Evonik Röhm Gmbh | Beschichtungszusammensetzung,(Meth)acryl-Polymer und Monomermischung zur Herstellung des(Meth)acryl-Polymers |
CN102459381A (zh) * | 2009-04-30 | 2012-05-16 | 阿姆斯特郎世界工业公司 | Uvv可固化的涂料组合物和使用其来涂覆地板和其他基材的方法 |
US8625944B1 (en) | 2009-05-13 | 2014-01-07 | Draka Comteq, B.V. | Low-shrink reduced-diameter buffer tubes |
US8625945B1 (en) | 2009-05-13 | 2014-01-07 | Draka Comteq, B.V. | Low-shrink reduced-diameter dry buffer tubes |
CN101811968B (zh) * | 2010-02-09 | 2014-07-30 | 深圳市有为化学技术有限公司 | 多官能团化苯甲酰甲酸羟基酮酯类化合物及含有该类化合物的光引发剂 |
EP2388239B1 (en) | 2010-05-20 | 2017-02-15 | Draka Comteq B.V. | Curing apparatus employing angled UV-LEDs |
US8871311B2 (en) | 2010-06-03 | 2014-10-28 | Draka Comteq, B.V. | Curing method employing UV sources that emit differing ranges of UV radiation |
DK2418183T3 (en) | 2010-08-10 | 2018-11-12 | Draka Comteq Bv | Method of curing coated glass fibers which provides increased UVLED intensity |
DK2638077T3 (en) * | 2010-11-12 | 2015-04-20 | Coloplast As | HOWEVER UNKNOWN POLYMER PHOTO INITIATORS |
JP6092229B2 (ja) * | 2011-10-06 | 2017-03-08 | フイルメニツヒ ソシエテ アノニムFirmenich Sa | 香料の放出のための感光性ラテックス |
EP2785307B1 (en) * | 2011-12-01 | 2019-06-26 | 3M Innovative Properties Company | One component self-adhesive dental composition, process of production and use thereof |
US8669281B1 (en) | 2013-03-14 | 2014-03-11 | Alkermes Pharma Ireland Limited | Prodrugs of fumarates and their use in treating various diseases |
CA2906580C (en) | 2013-03-14 | 2019-10-29 | Alkermes Pharma Ireland Limited | Prodrugs of fumarates and their use in treating various diseases |
CA2927948C (en) * | 2013-11-05 | 2022-04-26 | Construction Research & Technology Gmbh | Novel binding agent systems |
CN103709036B (zh) * | 2013-12-03 | 2015-07-29 | 天津久日化学股份有限公司 | 双官能团苯甲酰基甲酸羟基酮酯类化合物及含该类化合物的光引发剂 |
ES2753361T3 (es) | 2014-02-24 | 2020-04-08 | Alkermes Pharma Ireland Ltd | Sulfonamida y profármacos de fumaratos de sulfinamida y su uso en el tratamiento de diversas enfermedades |
KR20160142829A (ko) * | 2014-04-07 | 2016-12-13 | 바스프 에스이 | 주위 분위기에서의 광경화성 조성물의 가시광-경화 |
BR112017002974B1 (pt) * | 2014-08-17 | 2023-04-04 | Covestro (Netherlands) B.V | Método de revestimento de uma fibra óptica, composição líquida curável por radiação para o revestimento de uma fibra óptica e a referida fibra ótica |
JP7118580B2 (ja) * | 2014-08-26 | 2022-08-16 | キヤノン株式会社 | 光硬化性組成物、これを用いた硬化物パターンの製造方法、光学部品の製造方法、回路基板の製造方法、およびインプリント用モールドの製造方法 |
CN104387576B (zh) * | 2014-11-19 | 2016-06-29 | 浙江皇马科技股份有限公司 | 一种缩水甘油醚基封端烯丙醇无规聚醚的制备方法 |
JP5775239B1 (ja) | 2014-12-10 | 2015-09-09 | 互応化学工業株式会社 | 液状ソルダーレジスト組成物及び被覆プリント配線板 |
CN108473803B (zh) * | 2015-11-03 | 2021-11-12 | 3D系统公司 | 用于3d打印的生物相容性油墨 |
US20180033609A1 (en) * | 2016-07-28 | 2018-02-01 | QMAT, Inc. | Removal of non-cleaved/non-transferred material from donor substrate |
CN106905147A (zh) * | 2017-02-21 | 2017-06-30 | 怀化金鑫新材料有限公司 | 光引发剂苯甲酰甲酸二甘醇酯的合成新工艺 |
EP3597669A1 (en) | 2018-07-20 | 2020-01-22 | Clariant International Ltd | Photo-curable resin composition for 3d printing |
EP3597668A1 (en) | 2018-07-20 | 2020-01-22 | Clariant International Ltd | Photo-curable resin composition for 3d printing |
CN118027806B (zh) * | 2024-02-01 | 2024-08-09 | 江苏大自然智能家居有限公司 | 一种木地板用水性uv光固化涂料及其制备方法 |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3930868A (en) | 1973-05-23 | 1976-01-06 | The Richardson Company | Light sensitive arylglyoxyacrylate compositions |
DE2443645A1 (de) * | 1974-09-12 | 1976-04-01 | Cassella Farbwerke Mainkur Ag | Modifizierter aminoplast, verfahren zu seiner herstellung und seine verwendung |
US4038164A (en) | 1975-09-18 | 1977-07-26 | Stauffer Chemical Company | Photopolymerizable aryl and heterocyclic glyoxylate compositions and process |
US4024297A (en) * | 1976-02-02 | 1977-05-17 | Ppg Industries, Inc. | Actinic light polymerizable coating compositions |
DE2825955A1 (de) | 1978-06-14 | 1980-01-03 | Bayer Ag | Arylglyoxyloyloxyalkylacrylate und ihre verwendung in photopolymerisierbaren bindemitteln |
US4279720A (en) | 1978-07-13 | 1981-07-21 | Ciba-Geigy Corporation | Photocurable composition |
US4229274A (en) * | 1979-02-26 | 1980-10-21 | Ppg Industries, Inc. | Ultraviolet light curable compositions for producing coatings of low gloss |
US4475999A (en) | 1983-06-06 | 1984-10-09 | Stauffer Chemical Company | Sensitization of glyoxylate photoinitiators |
DE3512179A1 (de) * | 1985-04-03 | 1986-12-04 | Merck Patent Gmbh, 6100 Darmstadt | Fotoinitiatoren fuer die fotopolymerisation in waessrigen systemen |
DE3738567A1 (de) * | 1987-03-12 | 1988-09-22 | Merck Patent Gmbh | Coreaktive fotoinitiatoren |
TW328535B (en) * | 1993-07-02 | 1998-03-21 | Novartis Ag | Functional photoinitiators and their manufacture |
EP0849300A1 (de) * | 1996-12-19 | 1998-06-24 | Basf Aktiengesellschaft | Polyurethane mit kovalent gebundenen Photoinitiatoreinheiten |
ES2184233T3 (es) | 1997-01-30 | 2003-04-01 | Ciba Sc Holding Ag | Esteres fenilglioxalicos no volatiles. |
DE19913353A1 (de) | 1999-03-24 | 2000-09-28 | Basf Ag | Verwendung von Phenylglyoxalsäureestern als Photoinitiatoren |
DE10002089A1 (de) * | 2000-01-19 | 2001-07-26 | Basf Ag | Witterungsstabile, strahlungshärtbare Polyurethane |
RU2272022C2 (ru) * | 2000-06-23 | 2006-03-20 | Циба Спешиалти Кемикэлз Холдинг Инк. | Способ получения эфиров гидроксифенилкарбоновой кислоты |
TWI244495B (en) | 2000-08-14 | 2005-12-01 | Ciba Sc Holding Ag | Process for producing coatings siloxane photoinitiators |
TW557298B (en) | 2000-08-14 | 2003-10-11 | Ciba Sc Holding Ag | A compound, a photopolymerizible composition, a process for producing coatings and a method for causing a photoinitiator to accumulate at the surface of coatings |
WO2003089479A2 (en) * | 2002-04-19 | 2003-10-30 | Ciba Specialty Chemicals Holding Inc. | Curing of coatings induced by plasma |
DE10223614A1 (de) * | 2002-05-27 | 2003-12-11 | Basf Ag | Strahlungshärtbare wässrige Dispersionen |
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MXPA04010254A (es) | 2005-02-03 |
DE60304035D1 (en) | 2006-05-11 |
PL371516A1 (en) | 2005-06-27 |
KR100979660B1 (ko) | 2010-09-02 |
DE60304035T2 (de) | 2006-08-03 |
RU2320641C2 (ru) | 2008-03-27 |
AU2003233984A1 (en) | 2003-11-10 |
US7588880B2 (en) | 2009-09-15 |
EP1499645A1 (en) | 2005-01-26 |
RU2004134570A (ru) | 2005-07-20 |
TW200305582A (en) | 2003-11-01 |
DK1499645T3 (da) | 2006-07-17 |
CN1307207C (zh) | 2007-03-28 |
ES2259413T3 (es) | 2006-10-01 |
JP2005523923A (ja) | 2005-08-11 |
BR0309779B1 (pt) | 2013-06-25 |
CA2483004A1 (en) | 2003-11-06 |
ATE320452T1 (de) | 2006-04-15 |
BR0309779A (pt) | 2005-03-08 |
US20050228062A1 (en) | 2005-10-13 |
ZA200407897B (en) | 2006-02-22 |
KR20040106395A (ko) | 2004-12-17 |
PL207511B1 (pl) | 2010-12-31 |
CN1649905A (zh) | 2005-08-03 |
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