KR20040007700A - 결합된 구조를 가지는 옥심 에스테르 광개시제 - Google Patents
결합된 구조를 가지는 옥심 에스테르 광개시제 Download PDFInfo
- Publication number
- KR20040007700A KR20040007700A KR10-2003-7016235A KR20037016235A KR20040007700A KR 20040007700 A KR20040007700 A KR 20040007700A KR 20037016235 A KR20037016235 A KR 20037016235A KR 20040007700 A KR20040007700 A KR 20040007700A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- phenyl
- substituted
- halogen
- alkylene
- Prior art date
Links
- -1 Oxime ester Chemical class 0.000 title claims description 182
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 248
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 191
- 150000001875 compounds Chemical class 0.000 claims abstract description 80
- 239000001257 hydrogen Substances 0.000 claims abstract description 67
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 67
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 43
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 24
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims abstract description 21
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 18
- 229910052727 yttrium Inorganic materials 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims description 162
- 229910052736 halogen Inorganic materials 0.000 claims description 142
- 150000002367 halogens Chemical class 0.000 claims description 142
- 125000001624 naphthyl group Chemical group 0.000 claims description 85
- 125000001424 substituent group Chemical group 0.000 claims description 81
- 239000000758 substrate Substances 0.000 claims description 80
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 79
- 239000000049 pigment Substances 0.000 claims description 68
- 238000000034 method Methods 0.000 claims description 64
- 238000000576 coating method Methods 0.000 claims description 59
- 125000004432 carbon atom Chemical group C* 0.000 claims description 50
- 239000000463 material Substances 0.000 claims description 49
- 238000004519 manufacturing process Methods 0.000 claims description 46
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 45
- 229920001577 copolymer Polymers 0.000 claims description 40
- 229920005989 resin Polymers 0.000 claims description 39
- 239000011347 resin Substances 0.000 claims description 39
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 33
- 229920000642 polymer Polymers 0.000 claims description 29
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 26
- 239000000178 monomer Substances 0.000 claims description 26
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 23
- 125000001589 carboacyl group Chemical group 0.000 claims description 22
- 230000008569 process Effects 0.000 claims description 22
- 239000011230 binding agent Substances 0.000 claims description 21
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 claims description 20
- 230000003287 optical effect Effects 0.000 claims description 20
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 claims description 19
- 239000000843 powder Substances 0.000 claims description 19
- 239000011159 matrix material Substances 0.000 claims description 17
- 125000004957 naphthylene group Chemical group 0.000 claims description 16
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 15
- 239000000654 additive Substances 0.000 claims description 14
- 125000001038 naphthoyl group Chemical group C1(=CC=CC2=CC=CC=C12)C(=O)* 0.000 claims description 13
- 238000007639 printing Methods 0.000 claims description 13
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 12
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
- 239000003999 initiator Substances 0.000 claims description 12
- 239000000976 ink Substances 0.000 claims description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 10
- 239000012965 benzophenone Substances 0.000 claims description 9
- 229910000679 solder Inorganic materials 0.000 claims description 9
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 8
- 125000006729 (C2-C5) alkenyl group Chemical group 0.000 claims description 8
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 8
- 125000004414 alkyl thio group Chemical group 0.000 claims description 8
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 8
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 8
- 238000003384 imaging method Methods 0.000 claims description 7
- 125000006678 phenoxycarbonyl group Chemical group 0.000 claims description 7
- 239000003504 photosensitizing agent Substances 0.000 claims description 7
- 238000007650 screen-printing Methods 0.000 claims description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 6
- 238000005516 engineering process Methods 0.000 claims description 6
- 230000001070 adhesive effect Effects 0.000 claims description 5
- 239000002131 composite material Substances 0.000 claims description 5
- 125000000332 coumarinyl group Chemical group O1C(=O)C(=CC2=CC=CC=C12)* 0.000 claims description 5
- 125000004956 cyclohexylene group Chemical group 0.000 claims description 5
- 238000010894 electron beam technology Methods 0.000 claims description 5
- 238000009713 electroplating Methods 0.000 claims description 5
- 238000005530 etching Methods 0.000 claims description 5
- 239000003973 paint Substances 0.000 claims description 5
- 238000007747 plating Methods 0.000 claims description 5
- 239000002491 polymer binding agent Substances 0.000 claims description 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
- 239000000853 adhesive Substances 0.000 claims description 4
- 150000004056 anthraquinones Chemical class 0.000 claims description 4
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 claims description 4
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 4
- 238000012937 correction Methods 0.000 claims description 4
- 239000011152 fibreglass Substances 0.000 claims description 4
- 230000001678 irradiating effect Effects 0.000 claims description 4
- 239000003094 microcapsule Substances 0.000 claims description 4
- 229920000620 organic polymer Polymers 0.000 claims description 4
- 239000002966 varnish Substances 0.000 claims description 4
- 235000001671 coumarin Nutrition 0.000 claims description 3
- 238000005538 encapsulation Methods 0.000 claims description 3
- 238000004377 microelectronic Methods 0.000 claims description 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 2
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 2
- VWBYXJRDIQCSLW-UHFFFAOYSA-N O=[P](c1ccccc1)c1ccccc1 Chemical group O=[P](c1ccccc1)c1ccccc1 VWBYXJRDIQCSLW-UHFFFAOYSA-N 0.000 claims description 2
- 125000004423 acyloxy group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 150000008366 benzophenones Chemical class 0.000 claims description 2
- 230000005670 electromagnetic radiation Effects 0.000 claims description 2
- 238000001393 microlithography Methods 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 15
- 125000000753 cycloalkyl group Chemical group 0.000 abstract description 4
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 description 122
- 239000010410 layer Substances 0.000 description 80
- 239000010408 film Substances 0.000 description 43
- 239000011248 coating agent Substances 0.000 description 33
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 32
- 239000004973 liquid crystal related substance Substances 0.000 description 31
- 239000002904 solvent Substances 0.000 description 30
- 150000003254 radicals Chemical class 0.000 description 28
- 125000006850 spacer group Chemical group 0.000 description 24
- 239000000243 solution Substances 0.000 description 23
- 239000011342 resin composition Substances 0.000 description 22
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 21
- 239000007787 solid Substances 0.000 description 21
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 210000004027 cell Anatomy 0.000 description 16
- 238000010438 heat treatment Methods 0.000 description 16
- 239000000047 product Substances 0.000 description 16
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 15
- 239000011521 glass Substances 0.000 description 15
- 239000000126 substance Substances 0.000 description 15
- 239000002253 acid Substances 0.000 description 14
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 239000003960 organic solvent Substances 0.000 description 13
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
- 229910052757 nitrogen Inorganic materials 0.000 description 12
- 230000005855 radiation Effects 0.000 description 12
- 229920005862 polyol Polymers 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- 229920001187 thermosetting polymer Polymers 0.000 description 11
- 239000003513 alkali Substances 0.000 description 10
- 125000003118 aryl group Chemical group 0.000 description 10
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 10
- 239000006185 dispersion Substances 0.000 description 10
- 229920003002 synthetic resin Polymers 0.000 description 10
- 239000000057 synthetic resin Substances 0.000 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 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- 239000000975 dye Substances 0.000 description 9
- 150000003077 polyols Chemical class 0.000 description 9
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 9
- 239000011241 protective layer Substances 0.000 description 9
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 9
- 239000004642 Polyimide Substances 0.000 description 8
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 8
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
- 150000001735 carboxylic acids Chemical class 0.000 description 8
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 8
- 238000011161 development Methods 0.000 description 8
- 230000018109 developmental process Effects 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 8
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 8
- 239000011976 maleic acid Substances 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 238000000465 moulding Methods 0.000 description 8
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 8
- 238000000206 photolithography Methods 0.000 description 8
- 229920001721 polyimide Polymers 0.000 description 8
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 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
- 206010034972 Photosensitivity reaction Diseases 0.000 description 7
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 7
- 239000011229 interlayer Substances 0.000 description 7
- 229920003986 novolac Polymers 0.000 description 7
- 230000036211 photosensitivity Effects 0.000 description 7
- 239000000600 sorbitol Substances 0.000 description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
- 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 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 6
- 150000003926 acrylamides Chemical class 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 238000003491 array Methods 0.000 description 6
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 6
- AOJOEFVRHOZDFN-UHFFFAOYSA-N benzyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CC=C1 AOJOEFVRHOZDFN-UHFFFAOYSA-N 0.000 description 6
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 6
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 6
- ZJIPHXXDPROMEF-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O ZJIPHXXDPROMEF-UHFFFAOYSA-N 0.000 description 6
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 6
- 150000002576 ketones Chemical class 0.000 description 6
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 6
- 125000004430 oxygen atom Chemical group O* 0.000 description 6
- 238000000016 photochemical curing Methods 0.000 description 6
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- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 5
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 5
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 5
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 5
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
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- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 5
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- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 4
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- 239000002202 Polyethylene glycol Substances 0.000 description 4
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
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- 230000000996 additive effect Effects 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
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- 125000004555 carbazol-3-yl group Chemical group C1=CC(=CC=2C3=CC=CC=C3NC12)* 0.000 description 4
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- 239000003086 colorant Substances 0.000 description 4
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- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 4
- 150000002009 diols Chemical class 0.000 description 4
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- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
- GRPURDFRFHUDSP-UHFFFAOYSA-N tris(prop-2-enyl) benzene-1,2,4-tricarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C(C(=O)OCC=C)=C1 GRPURDFRFHUDSP-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
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 150000007964 xanthones Chemical class 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
- 239000011787 zinc oxide Substances 0.000 description 1
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/62—Oximes having oxygen atoms of oxyimino groups esterified
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- 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
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- Polymers & Plastics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Polymerisation Methods In General (AREA)
- Materials For Photolithography (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Pyrane Compounds (AREA)
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- Adhesives Or Adhesive Processes (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Description
광개시제의실시예 번호 | 광개시제농도 | 감광제 | 해당 노광 시간 후 재현된스탭의 갯수 | ||
40초 | 80초 | 160초 | |||
2 | 2.0% | - | 13 | 15 | 17 |
3 | 2.0% | - | 12 | 15 | 16 |
3 | 2.0% | S-2 | 13 | 15 | 17 |
4 | 2.0% | - | 12 | 14 | 16 |
5 | 0.5% | - | 11 | 13 | 15 |
1 | 2.0% | - | 14 | 17 | 19 |
8 | 2.0% | S-2 | 12 | 15 | 16 |
9 | 0.5% | - | 13 | 16 | 12 |
14 | 2.0% | - | 14 | 17 | 18 |
10 | 2.0% | - | 14 | 16 | 18 |
11 | 2.0% | - | 12 | 14 | 16 |
12 | 0.5% | - | 11 | 13 | 15 |
13 | 0.5% | - | 15 | 18 | 20 |
18 | 2.0% | - | 8 | 11 | 13 |
16 | 2.0% | - | 11 | 13 | 15 |
17 | 2.0% | - | 8 | 10 | 12 |
19 | 2.0% | - | 6 | 8 | 10 |
14 | 2.0% | - | 13 | 15 | 17 |
21 | 2.0% | - | 7 | 10 | 12 |
20 | 2.0% | - | 5 | 8 | 9 |
24 | 2.0% | - | 9 | 12 | 14 |
22 | 2.0% | - | 10 | 13 | 14 |
25 | 2.0% | - | 14 | 16 | 17 |
23 | 2.0% | - | 11 | 13 | 14 |
15 | 2.0% | - | 11 | 14 | 15 |
26 | 2.0% | - | 13 | 16 | 17 |
27 | 2.0% | - | 13 | 15 | 17 |
28 | 2.0% | - | 13 | 16 | 17 |
29 | 2.0% | - | 13 | 16 | 17 |
30 | 2.0% | - | 13 | 16 | 17 |
31 | 2.0% | - | 10 | 13 | 14 |
광개시제의실시예 번호 | 1000mJ/cm2로 노광시킨 후 재현된 스텝의 갯수 | ||
감광제 부재 | S-1 (EAB) | S-2 (ITX) | |
2 | 17 | - | - |
3 | 14 | 15 | 15 |
4 | 14 | - | - |
5 | 15 | - | - |
1 | 20 | - | - |
7 | 15 | - | - |
9 | 14 | - | - |
14 | 18 | - | - |
10 | 18 | - | - |
12 | 16 | - | - |
18 | - | 13 | 13 |
16 | 13 | 14 | 14 |
17 | - | - | 12 |
14 | 18 | - | 19 |
21 | 16 | - | - |
20 | - | - | 12 |
24 | 18 | - | - |
22 | 15 | - | 16 |
25 | 20 | - | - |
23 | 15 | - | - |
15 | 18 | - | - |
26 | 20 | - | - |
27 | 19 | - | - |
28 | 19 | - | - |
29 | 20 | - | - |
30 | 19 | - | - |
31 | 17 | - | - |
Claims (14)
- 하기 화학식 1, 화학식 2 및 화학식 3의 화합물:화학식 1화학식 2화학식 3위의 화학식 1, 화학식 2 및 화학식 3에서,R1은 수소이거나, 치환되지 않거나 하나 이상의 할로겐, 페닐 및/또는 CN에 의해 치환된 C3-C8사이클로알킬 또는 C1-C12알킬이거나; R1은 C2-C5알케닐이거나; R1은 치환되지 않거나 하나 이상의 C1-C6알킬, 할로겐, CN, OR3, SR4및/또는 NR5R6에 의해 치환된 페닐이거나; R1은 C1-C8알콕시 또는 벤질옥시이거나; 치환되지 않거나 하나이상의 C1-C6알킬 및/또는 할로겐에 의해 치환된 페녹시이고;R2및 R2'는 각각 독립적으로 수소이며; 치환되지 않은 C1-C20알킬이거나 하나 이상의 할로겐, OR3, 페닐 및/또는 치환기인 OR3, SR4및/또는 NR5R6에 의해 치환된 페닐에 의해 치환된 C1-C20알킬이거나; R2및 R2'는 C3-C8사이클로알킬이거나; R2및 R2'는 하나 이상의 -O-에 의해 차단되고/되거나 하나 이상의 할로겐, OR3, 페닐 및/또는 치환기인 OR3, SR4및/또는 NR5R6에 의해 치환된 페닐에 의해 임의로 치환된 C2-C20알킬이거나; R2및 R2'는 치환되지 않거나 하나 이상의 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 페닐이거나; R2및 R2'는 치환되지 않거나 하나 이상의 C1-C6알킬, 페닐, OR3, SR4및/또는 NR5R6에 의해 치환된 C2-C20알카노일 또는 벤조일이거나; R2및 R2'는 하나 이상의 -O-에 의해 임의로 차단되고/되거나 하나 이상의 하이드록실 그룹에 의해 임의로 치환된 C2-C12알콕시카보닐이거나; R2및 R2'는 치환되지 않거나 C1-C6알킬, 할로겐, 페닐, OR3, SR4및/또는 NR5R6에 의해 치환된 페녹시카보닐이거나; R2및 R2'는 CN, -CONR5R6, NO2, C1-C4할로알킬 또는 S(O)m-C1-C6알킬이거나; 임의로 C1-C12알킬 또는 SO2-C1-C6알킬에 의해 치환된 S(O)m-페닐이거나; C1-C12알킬에 의해 임의로 치환된 SO2O-페닐이거나; 디페닐 포스피노일또는 디-(C1-C4알콕시)-포스피노일이거나; R2및 R2'는(A),(B) 또는(C) 그룹이고;Ar1은 페닐, 나프틸, 벤조일 또는 나프토일이고, 이들은 각각 할로겐, C1-C12알킬, C3-C8사이클로알킬, 벤질 및/또는 페녹시카보닐에 의해 1 내지 7회 치환되거나; 각각 페닐, 또는 하나 이상의 OR3, SR4및/또는 NR5R6에 의해 치환된 페닐에 의해 치환되거나; 각각 하나 이상의 -O-에 의해 임의로 차단되고/되거나 하나 이상의 하이드록시 그룹에 의해 임의로 치환된 C2-C12알콕시카보닐에 의해 치환되거나; 각각 OR3, SR4, SOR4, SO2R4및/또는 NR5R6에 의해 치환(여기서, 치환기 OR3, SR4또는 NR5R6은, 페닐 환 또는 나프틸 환의 추가의 치환기와 함께, 라디칼 R3, R4, R5및/또는 R6을 통해 임의로 5원 또는 6원 환을 형성한다)되거나; 각각 -(CO)R7,(D),(E) 및/또는(F) 그룹에 의해 치환되고, 단 R2가 (A), (B) 또는 (C) 그룹이 아닌 경우, Ar1은 각각 적어도 하나의 -(CO)R7, (D), (E) 또는 (F) 그룹에 의해 치환된 페닐, 나프틸, 벤조일 또는 나프토일이고;Ar2는 페닐렌, 나프틸렌, 페닐렌디카보닐 또는 나프틸렌디카보닐이고, 이들은 각각 할로겐, C1-C12알킬, C3-C8사이클로알킬, 벤질, OR3, SR4, SOR4, SO2R4및/또는 NR5R6에 의해 1 내지 4회 치환되거나; 각각 -(CO)R7, (D), (E) 또는 (F) 그룹에 의해 치환되고; 단 R2또는 R2'가 (A), (B) 또는 (C) 그룹이 아니고 Ar2가 페닐렌, 나프틸렌, 페닐렌디카보닐 또는 나프틸렌디카보닐인 경우, Ar2는 적어도 하나의 -(CO)R7, (D), (E) 또는 (F) 그룹에 의해 치환되거나; R2가 수소 또는 (A), (B) 또는 (C) 그룹이 아닌 경우, Ar2는 각각 적어도 하나의 -(CO)R7, (D), (E) 또는 (F) 그룹에 의해 치환되거나, Ar2는 추가로또는이고, 이들은 치환되지 않거나 각각 할로겐, C1-C12알킬, 벤질, OR3, SR4, 및/또는 NR5R6에 의해 1 내지 4회 치환되거나; 각각 -(CO)R7, (D), (E) 또는 (F) 그룹에 의해 치환되고; R2가 (A), (B) 또는 (C) 그룹인 경우, Ar2는 추가로또는이고, 이들은 치환되지 않거나 각각 할로겐, C1-C12알킬, 벤질, OR3, SR4및/또는 NR5R6에 의해 1 내지 4회 치환되거나; 각각 -(CO)R7, (D), (E) 또는 (F) 그룹에 의해 치환되거나; Ar2는,,,,,,또는이고, 이들은 치환되지 않거나 각각 할로겐, C1-C12알킬, 벤질, OR3, SR4, 및/또는 NR5R6에 의해 1 내지 6회 치환(여기서, 치환기 OR3, SR4또는 NR5R6은, 페닐 환 또는 나프틸 환의 탄소원자들 중의 하나와 함께, 라디칼 R3, R4, R5및/또는 R6을 통해 임의로 5원 또는 6원 환을 형성한다)되거나; 각각 -(CO)R7, (D), (E) 또는 (F) 그룹에 의해 치환되고;Ar3은 페닐, 나프틸 또는 쿠마리닐이고, 이들은 각각 할로겐, C1-C12알킬, C3-C8사이클로알킬, 벤질 및/또는 페녹시카보닐에 의해 1회 내지 7회 치환되거나; 각각 페닐 또는 치환기인 하나 이상의 OR3, SR4및/또는 NR5R6로 치환된 페닐에 의해 치환되거나; 각각, 하나 이상의 -O-에 의해 임의로 차단되고/되거나 하나 이상의 하이드록시 그룹에 의해 임의로 치환된 C2-C12알콕시카보닐에 의해 치환되거나; 각각 OR3, SR4, SOR4, SO2R4및/또는 NR5R6에 의해 치환되고;M1은 하나 이상의 -O-에 의해 임의로 차단되고/되거나 하나 이상의 할로겐,OR3, 페닐 또는 치환기인 OR3, SR4및/또는 NR5R6에 의해 치환된 페닐에 의해 임의로 치환된 C1-C20알킬렌이거나; M1은 치환되지 않거나 각각 하나 이상의 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 페닐렌 또는 나프틸렌이거나; M1은 할로겐, C1-C12알킬, 벤질, OR3, SR4, SOR4, SO2R4및/또는 NR5R6에 의해 임의로 1 내지 4회 치환된(G) 또는(H) 그룹이고(여기서, 치환기 OR3, SR4또는 NR5R6은, 다른 페닐 환의 탄소원자들 중의 하나와 함께, 라디칼 R3, R4, R5및/또는 R6을 통해 임의로 5원 또는 6원 환을 형성한다), 단 Ar1이 각각 -(CO)R7, (D), (E) 또는 (F) 그룹에 의해 치환되지 않은 페닐, 나프틸, 벤조일 또는 나프토일인 경우, M1은 할로겐, C1-C12알킬, 벤질, OR3, SR4, SOR4, SO2R4및/또는 NR5R6에 의해 임의로 1 내지 4회 치환된 (G) 또는 (H) 그룹이고(여기서, 치환기 OR3, SR4또는 NR5R6은, 다른 페닐 환의 탄소원자들 중의 하나와 함께, 라디칼 R3, R4, R5및/또는 R6을 통해 임의로 5원 또는 6원 환을 형성한다);M2는 직접 결합, C1-C10알킬렌 또는 사이클로헥실렌이거나; M2는 각각 하나 이상의 -O-에 의해 임의로 차단되고/되거나 하나 이상의 할로겐, OR3, 페닐 또는 치환기인 OR3, SR4및/또는 NR5R6에 의해 치환된 페닐에 의해 임의로 치환된 C1-C10알킬렌또는 C1-C10알킬렌-X-이거나; M2는 치환되지 않거나 각각 하나 이상의 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 페닐렌, 나프틸렌 또는 페닐렌-X-이거나; M2는 C1-C10알킬렌-C(O)-X-, C1-C10알킬렌-X-C(O)-, 페닐렌-C(O)-X- 또는 C1-C10알킬렌-페닐렌-X-이고;M3및 M3'는 각각 서로 독립적으로 직접 결합, C1-C10알킬렌 또는 사이클로헥실렌이거나; M3및 M3'는 각각 하나 이상의 -O-에 의해 임의로 차단되고/되거나 하나 이상의 할로겐, OR3, 페닐 또는 치환기인 OR3, SR4및/또는 NR5R6에 의해 치환된 페닐에 의해 임의로 치환된 C1-C10알킬렌 또는 C1-C10알킬렌-X-이거나; M3및 M3'는 치환되지 않거나 각각 하나 이상의 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 페닐렌, 나프틸렌 또는 페닐렌-X-이거나; M3및 M3'는 C1-C10알킬렌-C(O)-X-, C1-C10알킬렌-X-C(O)-, 페닐렌-C(O)-X-, C1-C10알킬렌-페닐렌-X- 또는 페닐렌-C(O)-페닐렌이고, 단 M3및 M3'는, Ar1이 각각 -(CO)R7, (D), (E) 또는 (F) 그룹에 의해 치환되지 않은 나프틸, 나프토일 또는 2-R3O-페닐인 경우, C1-C10알킬렌-X-C(O)-, 페닐렌-X- 또는 C1-C10알킬렌-페닐렌-X-이 아니고;M4및 M4'는 각각 서로 독립적으로 직접 결합, -O-, -S-, -NR5'- 또는 -CO-이거나; M4및 M4'는 각각 하나 이상의 -O-에 의해 임의로 차단되고/되거나 하나 이상의 할로겐, OR3, 페닐 또는 치환기인 OR3, SR4및/또는 NR5R6에 의해 치환된 페닐에 의해 임의로 치환된 -Y-(C1-C10알킬렌)-Y'-이거나; M4및 M4'는 치환되지 않거나 각각 하나 이상의 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 -Y-페닐렌-Y'- 또는 -Y-나프틸렌-Y'-이거나; M4및 M4'는 -Y-(C1-C4알킬렌)-O-페닐렌-O-(C1-C4알킬렌)-Y'- 또는 -Y-(C1-C4알킬렌)-O-나프틸렌-O-(C1-C4알킬렌)-Y'-이거나; M4및 M4'는 하나 이상의 -O-에 의해 임의로 차단된 -X-C1-C10알킬렌-X-C(O)-이거나; M4및 M4'는 할로겐, C1-C12알킬, 벤질, OR3, SR4, SOR4, SO2R4및/또는 NR5R6에 의해 임의로 1 내지 4회 치환된그룹이고(여기서, 치환기 OR3, SR4또는 NR5R6은, 당해 그룹이 결합된 페닐 환 또는 나프틸 환의 탄소원자들 중의 하나와 함께 또는 다른 페닐 환의 탄소원자들 중의 하나와 함께 라디칼 R3, R4, R5및/또는 R6을 통해 임의로 5원 또는 6원 환을 형성한다);M4"는 직접 결합, -O-, -S-, -NR5'- 또는 -CO-이거나; M4"는 하나 이상의 -O-에 의해 임의로 차단되고/되거나 하나 이상의 할로겐, OR3, 페닐 또는 치환기인 OR3, SR4및/또는 NR5R6에 의해 치환된 페닐에 의해 임의로 치환된 -Y-(C1-C4알킬렌)-Y'-이거나; M4"는 치환되지 않거나 각각 하나 이상의 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 -Y-페닐렌-Y'- 또는 -Y-나프틸렌-Y'-이거나; M4"는 하나 이상의 -O-에 의해 임의로 차단된 -X-C1-C10알킬렌-X-C(O)-이고;X 및 X'는 각각 서로 독립적으로 -O-, -S- 또는 -NR5-이고;Y 및 Y'는 각각 서로 독립적으로 직접 결합, -O-, -S- 또는 -NR5-이고;R3은 수소, C1-C20알킬 또는 페닐-C1-C3알킬이거나; R3은 -OH, -SH, -CN, C3-C6알켄옥실, -OCH2CH2CN, -OCH2CH2(CO)O(C1-C4알킬), -O(CO)-(C1-C4알킬), -O(CO)-페닐, -(CO)OH 및/또는 -(CO)O(C1-C4알킬)에 의해 치환된 C1-C8알킬이거나; R3은 하나 이상의 -O-에 의해 차단된 C2-C12알킬이거나; R3은 -(CH2CH2O)n+1H, -(CH2CH2O)n(CO)-(C1-C8알킬), C1-C8알카노일, C2-C12알케닐, C3-C6알케노일, C3-C8사이클로알킬이거나; R3은 치환되지 않거나 하나 이상의 C1-C6알킬, 할로겐, -OH 및/또는 C1-C4알콕시에 의해 치환된 벤조일이거나; R3은 치환되지 않거나 각각 할로겐, -OH, C1-C12알킬, C1-C12알콕시, 페녹시, C1-C12알킬설파닐, 페닐설파닐, -N(C1-C12알킬)2및/또는 디페닐아미노에 의해 치환된 페닐 또는 나프틸이고;n은 1 내지 20이고;R4는 수소, C1-C20알킬, C2-C12알케닐, C3-C8사이클로알킬, 페닐-C1-C3알킬이거나; R4는 -OH, -SH, -CN, C3-C6알켄옥실, -OCH2CH2CN, -OCH2CH2(CO)O(C1-C4알킬), -O(CO)-(C1-C4알킬), -O(CO)-페닐, -(CO)OH 또는 -(CO)O(C1-C4알킬)에 의해 치환된 C1-C8알킬이거나; R4는 하나 이상의 -O- 또는 -S-에 의해 차단된 C2-C12알킬이거나; R4는 -(CH2CH2O)n+1H, -(CH2CH2O)n(CO)-(C1-C8알킬), C1-C8알카노일, C2-C12알케닐, C3-C6알케노일이거나; R4는 치환되지 않거나 하나 이상의 C1-C6알킬, 할로겐, -OH, C1-C4알콕시 또는 C1-C4알킬설파닐에 의해 치환된 벤조일이거나; R4는 치환되지 않거나 각각 할로겐, C1-C12알킬, C1-C12알콕시, 페닐-C1-C3알콕시, 페녹시, C1-C12알킬설파닐, 페닐설파닐, -N(C1-C12알킬)2, 디페닐아미노, -(CO)O(C1-C8알킬), -(CO)-C1-C8알킬 또는 (CO)N(C1-C8알킬)2에 의해 치환된 페닐 또는 나프틸이고;R5및 R6은 각각 서로 독립적으로 수소, C1-C20알킬, C2-C4하이드록시알킬, C2-C10알콕시알킬, C2-C5알케닐, C3-C8사이클로알킬, 페닐-C1-C3알킬, C1-C8알카노일, C3-C12알케노일 또는 벤조일이거나; R5및 R6은 치환되지 않거나 각각 C1-C12알킬, 벤조일 또는 C1-C12알콕시에 의해 치환된 페닐 또는 나프틸이거나; R5및 R6은 함께 -O- 또는 -NR3-에 의해 임의로 차단되고/되거나 하이드록시, C1-C4알콕시, C2-C4알카노일옥시 또는 벤조일옥시에 의해 임의로 치환된 C2-C6알킬렌이고;R5'는 수소, C1-C20알킬, C2-C4하이드록시알킬, C2-C10알콕시알킬, C2-C5알케닐, C3-C8사이클로알킬, 페닐-C1-C3알킬, C2-C8알카노일, C3-C12알케노일 또는 벤조일이거나; R5'는 치환되지 않거나 각각 C1-C12알킬 또는 C1-C12알콕시에 의해 치환된 페닐 또는 나프틸이거나; R5'는그룹이고;R7은 수소 또는 C1-C20알킬이거나; 할로겐, 페닐, -OH, -SH, -CN, C3-C6알케녹시, -OCH2CH2CN, -OCH2CH2(CO)O(C1-C4알킬), -O(CO)-(C1-C4알킬), -O(CO)-페닐, -(CO)OH 또는 -(CO)O(C1-C4알킬)에 의해 치환된 C1-C8알킬이거나; R7은 하나 이상의 -O-에 의해 차단된 C2-C12알킬이거나; R7은 -(CH2CH2O)n+1H, -(CH2CH2O)n(CO)-(C1-C8알킬), C2-C12알케닐 또는 C3-C8사이클로알킬이거나; R7은 각각 하나 이상의 C1-C6알킬, 할로겐, CN, OR3, SR4, SOR4, SO2R4또는 NR5R6에 의해 임의로 치환된 페닐, 비페닐릴 또는 나프틸(여기서, 치환기 OR3, SR4또는 NR5R6은, 페닐, 비페닐릴 또는 나프틸 환의 탄소원자들 중의 하나와 함께, 라디칼 R3, R4, R5및/또는 R6을 통해 임의로 5원 또는 6원 환을 형성한다)이고;R8, R9, R8' 및 R9'는 각각 서로 독립적으로 수소, 치환기인 하나 이상의 할로겐, 페닐, CN, -OH, -SH, C1-C4알콕시, -(CO)OH 또는 -(CO)O(C1-C4알킬)에 의해 임의로 치환된 C1-C12알킬이거나; R8, R9, R8' 및 R9'는 하나 이상의 C1-C6알킬, 할로겐, CN, OR3, SR4또는 NR5R6에 의해 임의로 치환된 페닐이거나; R8, R9, R8' 및 R9'는 할로겐, CN, OR3, SR4, SOR4, SO2R4또는 NR5R6(여기서, 치환기 OR3, SR4또는 NR5R6은, Ar1의 페닐, 나프틸, 벤조일 또는 나프토일 그룹의 탄소원자들 중의 하나와 함께 또는 치환기 R7의 탄소원자들 중의 하나와 함께 또는 M3의 나프틸렌 또는 페닐렌 그룹의 탄소원자들 중의 하나와 함께, 라디칼 R3, R4, R5및/또는 R6을 통해 임의로 5원 또는 6원 환을 형성한다)이거나; R8과R9,또는 R8'와 R9'는 함께또는그룹이고;R10, R11, R12및 R13은 서로 독립적으로 수소, 치환기인 하나 이상의 할로겐, 페닐, CN, -OH, -SH, C1-C4알콕시, -(CO)OH 또는 -(CO)O(C1-C4알킬)에 의해 임의로 치환된 C1-C12알킬이거나; R10, R11, R12및 R13은 하나 이상의 C1-C6알킬, 할로겐, CN, OR3, SR4또는 NR5R6에 의해 임의로 치환된 페닐이거나; R10, R11, R12및 R13은 할로겐, CN, OR3, SR4또는 NR5R6이고;R14및 R15는 서로 독립적으로 수소, 치환기인 하나 이상의 할로겐, 페닐, CN, -OH, -SH, C1-C4알콕시, -(CO)OH 또는 -(CO)O(C1-C4알킬)에 의해 임의로 치환된C1-C12알킬이거나; R14및 R15는 하나 이상의 C1-C6알킬, 할로겐, CN, OR3, SR4또는 NR5R6에 의해 임의로 치환된 페닐이고, 단(ⅰ) Ar1이 (E) 그룹에 의해 치환되고 (D) 또는 (F) 그룹에 의해 추가로 치환되지 않은 페닐이며 R2가 수소인 경우, M4는 직접 결합, S 또는 NR5이 아니고,(ⅱ) Ar1이 (E) 그룹에 의해 치환되고 (D) 또는 (F) 그룹에 의해 추가로 치환되지는 않은 나프틸인 경우, M4는 직접 결합, S 또는 NR5이 아니며,(ⅲ) M4가 O이고 R2가 수소인 경우, Ar1은 (E) 그룹에 의해 치환되고 (D) 또는 (F) 그룹에 의해 추가로 치환되지는 않으며, 동시에 오르토 위치에서 OR3에 의해 또는 SR4, NR5R6, -(CO)R7또는 SO2R7에 의해 치환된 페닐이 아니고,(ⅳ) Ar1이 -(CO)R7에 의해 치환되고 (D) 또는 (F) 그룹에 의해 추가로 치환되지 않은 페닐인 경우, R2는 수소가 아니며,(ⅴ) Ar1이 -(CO)R7에 의해 치환되고 (D) 또는 (F) 그룹에 의해 추가로 치환되지 않은 페닐이고 R2가 수소가 아닌 경우, R7는 페닐 또는 C1-C11알킬이 아니고,(ⅵ) Ar1이 -(CO)R7에 의해 치환되고 (D) 또는 (F) 그룹에 의해 추가로 치환되지 않은 나프틸인 경우, R7은 페닐 또는 C1-C11알킬이 아니다.
- 제1항에 있어서,R1은 치환되지 않거나 하나 이상의 할로겐 또는 페닐에 의해 치환된 C3-C6사이클로알킬 또는 C1-C6알킬이거나; R1은 치환되지 않거나 하나 이상의 C1-C6알킬, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 페닐이거나; R1은 C1-C6알콕시 또는 벤질옥시이고;R2및 R2'는 각각 서로 독립적으로 수소이고; 하나 이상의 할로겐, OR3, 페닐 및/또는 치환기인 OR3, SR4및/또는 NR5R6에 의해 치환된 페닐에 의해 임의로 치환된 C1-C20알킬이거나; C3-C6사이클로알킬이거나; 하나 이상의 -O-에 의해 차단되고/되거나 하나 이상의 할로겐, OR3, 페닐 및/또는 치환기인 OR3, SR4및/또는 NR5R6에 의해 치환된 페닐에 의해 임의로 치환된 C2-C20알킬이거나; R2및 R2'는 치환되지 않거나 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 페닐이거나; R2및 R2'는 C2-C12알카노일, C2-C12알콕시카보닐 또는 (A), (B) 또는 (C)그룹이고;Ar1은 페닐, 나프틸 또는 벤조일이고, 이들은 각각 할로겐, C1-C6알킬, OR3, SR4및/또는 NR5R6에 의해 1회 내지 7회 치환거나; 각각 페닐 또는 치환기인 하나 이상의 OR3, SR4또는 NR5R6에 의해 치환된 페닐에 의해 치환되거나; 각각 -(CO)R7, (D), (E) 및/또는 (F) 그룹에 의해 치환되고;Ar2는 각각 할로겐, C1-C6알킬, OR3, SR4및/또는 NR5R6에 의해 1회 내지 4회 치환된 페닐렌 또는 페닐렌디카보닐이거나; Ar2는또는이고, 이들은 치환되지 않거나 각각 할로겐, C1-C6알킬, OR3, SR4및/또는 NR5R6에 의해 1 내지 4회 치환되거나; 각각 -(CO)R7, (D), (E) 또는 (F) 그룹에 의해 치환되거나; Ar2는,또는이고, 이들은 치환되지 않거나 각각 할로겐, C1-C6알킬, OR3, SR4및/또는 NR5R6에 의해 1 내지 6회 치환(여기서, 치환기 OR3, SR4및/또는 NR5R6은, 페닐 환의 탄소원자들 중의 하나와 함께, 라디칼 R3, R4, R5및/또는 R6을 통해 5원 또는 6원 환을 임의로 형성한다)되거나; 각각 -(CO)R7, (D), (E) 및/또는 (F) 그룹에 의해 치환되고;Ar3은 페닐, 나프틸 또는 쿠마리닐이고, 이들은 각각 할로겐, C1-C12알킬, 페닐 또는 치환기인 하나 이상의 OR3, SR4및/또는 NR5R6에 의해 치환된 페닐에 의해 1 내지 7회 치환되나; 각각 OR3, SR4및/또는 NR5R6에 의해 치환되고;M1은 하나 이상의 -O-에 의해 임의로 차단된 C1-C20알킬렌이거나; M1은 페닐렌또는 나프틸렌이고, 이들은 치환되지 않거나 각각 하나 이상의 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환되거나; M1은 할로겐, C1-C6알킬, OR3, SR4및/또는 NR5R6에 의해 임의로 1 내지 4회 치환된 (H) 그룹(여기서, 치환기 OR3, SR4및/또는 NR5R6은, 페닐 환의 탄소원자들 중의 하나와 함께, 라디칼 R3, R4, R5및/또는 R6을 통해 5원 또는 6원 환을 임의로 형성한다)이고;M2는 직접 결합, 각각 하나 이상의 -O-에 의해 임의로 차단된 C1-C10알킬렌 또는 C1-C10알킬렌-O-이거나; M2는 치환되지 않거나 하나 이상의 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 페닐렌-O-이거나; M2는 C1-C6알킬렌-페닐렌-O-이고;M3및 M3'는 각각 서로 독립적으로 직접 결합이거나, 각각 하나 이상의 -O-에 의해 임의로 차단된 C1-C10알킬렌 또는 C1-C10알킬렌-X-이거나; M3및 M3'는 치환되지 않거나 각각 하나 이상의 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 페닐렌 또는 페닐렌-X-이거나; M3및 M3'는 C1-C10알킬렌-C(O)-X-, C1-C10알킬렌-X-C(O)-, 페닐렌-C(O)-X-, C1-C6알킬렌-페닐렌-X- 또는 페닐렌-C(O)-페닐렌이고;M4및 M4'는 각각 서로 독립적으로 직접 결합, -O-, -S-, -NR5'- 또는 -CO-이거나; M4및 M4'는 하나 이상의 -O-에 의해 임의로 차단된 -Y-(C1-C10알킬렌)-Y'-이거나; M4및 M4'는 치환되지 않거나 하나 이상의 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 -Y-페닐렌-Y'-이거나; M4및 M4'는 -Y-(C1-C4알킬렌)-O-페닐렌-O-(C1-C4알킬렌)-Y'- 또는 -Y-(C1-C4알킬렌)-O-나프틸렌-O-(C1-C4알킬렌)-Y'-이거나; M4및 M4'는 하나 이상의 -O-에 의해 임의로 차단된 -X-C1-C10알킬렌-X-C(O)-이거나; M4및 M4'는 할로겐, C1-C12알킬렌, OR3, SR4및/또는 NR5R6에 의해 1회 내지 4회 치환된그룹(여기서, 치환기 OR3, SR4및/또는 NR5R6은, 당해 그룹이 결합된 페닐 환 또는 나프틸 환의 탄소원자들 중의 하나와 함께 또는 다른 페닐 환의 탄소원자들 중의 하나와 함께, 라디칼 R3, R4, R5및/또는 R6을 통해 5원 또는 6원 환을 임의로 형성한다)이고;M4"는 직접 결합, -O-, -S-, -NR5'- 또는 -CO-이거나; M4"는 하나 이상의 -O-에 의해 임의로 차단된 -Y-(C1-C10알킬렌)-Y'-이거나; M4"는 치환되지 않거나 하나 이상의 C1-C6알킬, 페닐, 할로겐, OR3, SR4및/또는 NR5R6에 의해 치환된 -Y-페닐렌-Y'-이거나; M4"는 하나 이상의 -O-에 의해 임의로 차단된 -X-C1-C10알킬렌-X-C(O)-이고;R3은 수소, C1-C20알킬 또는 페닐-C1-C3알킬이거나; R3은 C3-C6알케녹시, -O(CO)-(C1-C4알킬) 또는 -O(CO)-페닐에 의해 치환된 C1-C8알킬이거나; R3은 하나 이상의 -O-에 의해 임의로 차단된 C2-C12알킬이거나; R3은 C1-C8알카노일이거나; 치환되지 않거나 하나 이상의 C1-C6알킬, 할로겐 및/또는 C1-C4알콕시에 의해 치환된 벤조일이거나; R3은 치환되지 않거나 할로겐, C1-C12알킬, C1-C4알콕시, C1-C12알킬설파닐, 페닐설파닐, -N(C1-C12알킬)2및/또는 디페닐아미노에 의해 치환된 페닐 또는 나프틸이고;R4는 수소, C1-C20알킬 또는 페닐-C1-C3알킬이거나; R4는 C3-C6알케녹시, -O(CO)-(C1-C4알킬) 또는 -O(CO)-페닐에 의해 치환된 C1-C8알킬이거나; R4는 하나 이상의 -O- 또는 -S-에 의해 임의로 차단된 C2-C12알킬이거나; R4는 C1-C8알카노일이거나; 치환되지 않거나 하나 이상의 C1-C6알킬, 할로겐, C1-C4알콕시 또는 C1-C4알킬설파닐에 의해 치환된 벤조일이거나; R4는 치환되지 않거나 할로겐, C1-C12알킬, C1-C12알콕시, 페녹시, C1-C12알킬설파닐, 페닐설파닐, -N(C1-C12알킬)2, 디페닐아미노 또는 -(CO)(C1-C8알킬)에 의해 치환된 페닐 또는 나프틸이고;R5및 R6은 각각 서로 독립적으로 수소, C1-C20알킬, C2-C10알콕시알킬, 페닐-C1-C3알킬, C1-C8알카노일 또는 벤조일이거나; R5및 R6은 치환되지 않거나 각각 벤조일, C1-C12알킬 또는 C1-C12알콕시에 의해 치환된 페닐 또는 나프틸이거나; R5및 R6은 함께 -O- 또는 -NR3-에 의해 임의로 차단되고/되거나 C1-C4알콕시, C2-C4알카노일옥시 또는 벤조일옥시에 의해 임의로 치환된 C2-C6알킬렌이고;R5'는 수소, C1-C10알킬 또는 C2-C4하이드록시알킬이거나; R5'는 치환되지 않거나 각각 C1-C6알킬 또는 C1-C6알콕시에 의해 치환된 페닐 또는 나프틸이거나; R5'는그룹이고;R7은 수소 또는 C1-C20알킬이거나; 페닐, -OH-, -O(CO)-(C1-C4알킬) 또는 -O(CO)-페닐에 의해 치환된 C1-C8알킬이거나; R7은 C2-C5알케닐 또는 C3-C8사이클로알킬이거나; R7은 각각 하나 이상의 C1-C6알킬, 할로겐, CN, OR3, SR4또는 NR5R6에 의해 임의로 치환된 페닐, 비페닐릴 또는 나프틸이고;R8, R9, R8' 및 R9'는 각각 서로 독립적으로 수소 또는 C1-C6알킬이거나; 하나 이상의 C1-C6알킬, 할로겐, OR3, SR4또는 NR5R6에 의해 임의로 치환된 페닐이거나; R8, R9, R8' 및 R9'는 할로겐, OR3, SR4또는 NR5R6(여기서, 치환기 OR3, SR4또는 NR5R6은, Ar1의 페닐, 나프틸 또는 벤조일 그룹의 탄소원자들 중의 하나와 함께 또는 치환기 R7의 탄소원자들 중의 하나와 함께, 라디칼 R3, R4, R5및/또는 R6을 통해 5원 또는 6원 환을 임의로 형성한다)이거나; R8과 R9, 또는 R8'와 R9'는 함께그룹이고;R10, R11, R12및 R13은 서로 독립적으로 수소, C1-C6알킬, 페닐, 할로겐, OR3, SR4또는 NR5R6인, 화학식 1, 화학식 2 및 화학식 3의 화합물.
- 제1항에 있어서,R1은 C1-C12알킬 또는 페닐이고;R2및 R2'는 수소 또는 C1-C12알킬, 페닐 또는 C2-C12알콕시카보닐이고;Ar1은 페닐, 나프틸 또는 벤조일이고, 이들은 각각 OR3또는 NR5R6에 의해 치환(여기서, 치환기 NR5R6은, 페닐 환 또는 나프틸 환의 추가의 치환기와 함께, 라디칼 R5또는 R6을 통해 5원 또는 6원 환을 임의로 형성한다)되거나; -C(O)R7, (D), (E) 또는 (F) 그룹에 의해 치환되고;Ar2는이고;Ar3은 나프틸이고;M4및 M4'는 각각 서로 독립적으로 직접 결합, -O-, -S- 또는 -Y-(C1-C10알킬렌)-Y'- 또는 -Y-(C1-C4알킬렌)-O-페닐렌-O-(C1-C4알킬렌)Y'-이고;Y 및 Y'는 각각 서로 독립적으로 직접 결합 또는 -O-이고;R3은 C1-C12알킬이고;R4는 치환되지 않거나 -(CO)(C1-C8알킬)에 의해 치환된 페닐이고;R5및 R6은 각각 서로 독립적으로 C1-C12알킬이거나; 치환되지 않거나 벤조일 또는 C1-C12알킬에 의해 치환된 페닐이고;R7은 각각 하나 이상의 C1-C6알킬, 할로겐, OR3, SR4또는 NR5R6에 의해 임의로 치환된 페닐, 비페닐릴 또는 나프틸이고;R8및 R9는 수소 또는 NR5R6(여기서, 치환기 NR5R6은, Ar1의 페닐, 나프틸, 또는 벤조일 그룹의 탄소원자들 중의 하나와 함께, 라디칼 R5또는 R6을 통해 5원 또는 6원 환을 임의로 형성한다)인, 화학식 1 또는 화학식 3의 화합물.
- 적어도 하나의 에틸렌성 불포화 광중합성 조성물(a) 및 광개시제로서 제1항에 따르는 화학식 1, 화학식 2 및 화학식 3의 화합물(b) 적어도 하나를 포함하는 광중합성 조성물.
- 제4항에 있어서, 광개시제(b) 이외에 적어도 하나의 추가의 광개시제(c) 및/또는 기타 첨가제(d)를 포함하는 광중합성 조성물.
- 제4항 또는 제5항에 있어서, 조성물을 기준으로 하여, 광개시제(b), 또는 광개시제(b)와 광개시제(c)를 0.05중량% 내지 25중량% 포함하는 광중합성 조성물.
- 제5항 또는 제6항에 있어서, 감광제, 특히 벤조페논 및 이의 유도체, 티오크산톤 및 이의 유도체, 안트라퀴논 및 이의 유도체, 및 쿠마린 및 이의 유도체로 이루어진 그룹으로부터 선택된 화합물을 포함하는 추가의 첨가제(d)를 포함하는 광중합성 조성물.
- 제4항 내지 제7항 중의 어느 한 항에 있어서, 결합제 중합체(e), 특히 메타크릴레이트와 메타크릴산의 공중합체를 포함하는 광중합성 조성물.
- 제4항 내지 제9항 중의 어느 한 항에 따르는 조성물에 150 내지 600nm 범위의 전자기 복사선을 조사하거나 전자빔 또는 X선을 조사하는 것을 포함하는, 에틸렌성 불포화 이중 결합을 포함하는 화합물의 광중합 반응방법.
- 착색된 페인트 및 착색되지 않은 페인트 및 와니스, 분말 피복물, 인쇄용 잉크, 인쇄판, 접착제, 치과용 조성물, 겔 피복물, 전기도금 레지스트와 같은 전자공학용 감광성 레지스트, 식각 레지스트, 습식 및 건식 필름 및 솔더 레지스트를 제조하기 위한; 다양한 디스플레이 제품에 필요한 컬러 필터를 제조하거나 플라즈마 디스플레이 패널, 전기발광 디스플레이 및 LCD의 제조 공정에서 구조물을 형성하기위한 레지스트로서의; 전기 및 전자 부품의 캡슐화를 위한 조성물로서의; 자기 기록 물질, 마이크로기계 부품, 도파관, 광스위치, 도금 마스크, 식각 마스크, 색상 교정 시스템, 유리 섬유 케이블 피복물, 스크린 인쇄용 스텐실을 제조하기 위한; 스테레오리소그래피 방식에 의해 3차원 물체를 제조하기 위한; 영상 기록 물질로서의, 특히 홀로그래피 기록용 영상 기록 물질로서의; 마이크로전자회로, 탈색 물질, 영상 기록 물질용 탈색 물질, 마이크로캡슐을 이용하는 영상 기록 물질을 위한; UV 및 가시영역 레이저 이미징 시스템용 감광성 레지스트 물질로서의; 인쇄 회로판의 시퀀셜 빌드-업 층(sequential build-up layer)에 유전체층을 형성하는 데 사용되는 감광성 레지스트 물질로서의, 제4항 내지 제9항 중의 어느 한 항에 따르는 조성물의 용도.
- 제9항에 있어서, 착색된 페인트 및 착색되지 않은 페인트 및 와니스, 분말 피복물, 인쇄용 잉크, 인쇄판, 접착제, 치과용 조성물, 겔 피복물, 전기도금 레지스트와 같은 전자공학용 감광성 레지스트, 식각 레지스트, 습식 및 건식 필름 및 솔더 레지스트를 제조하기 위한; 다양한 디스플레이 제품에 필요한 컬러 필터를 제조하거나 플라즈마 디스플레이 패널, 전기발광 디스플레이 및 LCD의 제조 공정에서 구조물을 형성하기 위한 레지스트로서의; 복합 조성물을 위한; 감광성 레지스트를 포함하는 레지스트를 위한; 컬러 필터 물질을 위한; 전기 및 전자 부품의 캡슐화를 위한 조성물로서의; 자기 기록 물질, 마이크로기계 부품, 도파관, 광스위치, 도금 마스크, 식각 마스크, 색상 교정 시스템, 유리 섬유 케이블 피복물, 스크린 인쇄용스텐실을 제조하기 위한; 마이크로리소리소그래피, 도금, 스테레오리소그래피 방식에 의해 3차원 물체를 제조하기 위한; 영상 기록 물질, 특히 홀로그래피 기록용 영상 기록 물질, 마이크로전자회로, 마이크로캡슐을 이용하는 영상 기록 물질용 탈색물질을 제조하기 위한; 인쇄 회로판의 시퀀셜 빌드-업 층에 유전체층을 형성하기 위한; 특히 직접 이미징 기술의 광원으로 UV 및 가시영역 레이저를 사용하는 공정을 위한, 광중합 반응방법.
- 제4항에 따르는 조성물이 적어도 한쪽 표면에 피복되어 있는, 피복된 기판.
- 제12항에 따르는 피복된 기판을 화상에 따라 노광시킨 후, 현상제로 비노광 영역을 제거함을 포함하여, 릴리프 화상을 사진술로 제조하는 방법.
- 다관능성 아크릴레이트 단량체, 유기 중합체 결합제 및 제1항에 따르는 화학식 1, 화학식 2 및 화학식 3의 광중합 개시제를 포함하는 감광성 수지 및 안료를 포함하는 적색, 녹색, 청색 화소 및 흑색 매트릭스를 투명 기판 위에 제공하고, 투명 기판의 표면 또는 컬러 필터층의 표면 위에 투명 전극을 제공함으로써 제조되는 컬러 필터.
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PCT/EP2002/006107 WO2002100903A1 (en) | 2001-06-11 | 2002-06-04 | Oxime ester photoinitiators having a combined structure |
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Also Published As
Publication number | Publication date |
---|---|
TW593357B (en) | 2004-06-21 |
WO2002100903A1 (en) | 2002-12-19 |
JP3860170B2 (ja) | 2006-12-20 |
ATE446322T1 (de) | 2009-11-15 |
EP1395615B1 (en) | 2009-10-21 |
CA2446722A1 (en) | 2002-12-19 |
DE60234095D1 (de) | 2009-12-03 |
JP2004534797A (ja) | 2004-11-18 |
KR100801457B1 (ko) | 2008-02-11 |
EP1395615A1 (en) | 2004-03-10 |
CN1514845A (zh) | 2004-07-21 |
CN100528838C (zh) | 2009-08-19 |
US7189489B2 (en) | 2007-03-13 |
US20040170924A1 (en) | 2004-09-02 |
JP2006342166A (ja) | 2006-12-21 |
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