TWI798372B - 新穎之二官能(甲基)丙烯酸酯化合物及聚合物 - Google Patents
新穎之二官能(甲基)丙烯酸酯化合物及聚合物 Download PDFInfo
- Publication number
- TWI798372B TWI798372B TW108107162A TW108107162A TWI798372B TW I798372 B TWI798372 B TW I798372B TW 108107162 A TW108107162 A TW 108107162A TW 108107162 A TW108107162 A TW 108107162A TW I798372 B TWI798372 B TW I798372B
- Authority
- TW
- Taiwan
- Prior art keywords
- reaction
- bis
- meth
- cyclohexyl
- formula
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims description 29
- 150000001252 acrylic acid derivatives Chemical class 0.000 title description 5
- 230000001588 bifunctional effect Effects 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 30
- 229920005989 resin Polymers 0.000 claims abstract description 18
- 239000011347 resin Substances 0.000 claims abstract description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 5
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 36
- 239000011342 resin composition Substances 0.000 claims description 15
- 239000003431 cross linking reagent Substances 0.000 claims description 7
- 239000000470 constituent Substances 0.000 claims description 2
- 230000035945 sensitivity Effects 0.000 abstract description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 6
- 238000005530 etching Methods 0.000 abstract description 5
- 229910052799 carbon Inorganic materials 0.000 abstract description 2
- 238000006243 chemical reaction Methods 0.000 description 41
- -1 coatings Substances 0.000 description 30
- 239000000178 monomer Substances 0.000 description 28
- 239000002904 solvent Substances 0.000 description 28
- 229920001577 copolymer Polymers 0.000 description 22
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 19
- 239000002253 acid Substances 0.000 description 19
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- 239000000243 solution Substances 0.000 description 16
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 238000005984 hydrogenation reaction Methods 0.000 description 15
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 15
- 239000010408 film Substances 0.000 description 14
- 230000015572 biosynthetic process Effects 0.000 description 13
- 239000003054 catalyst Substances 0.000 description 13
- 239000001257 hydrogen Substances 0.000 description 13
- 229910052739 hydrogen Inorganic materials 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 12
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 12
- 239000013078 crystal Substances 0.000 description 12
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 11
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- 238000003786 synthesis reaction Methods 0.000 description 10
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 9
- LZVABRWSXQNGJP-UHFFFAOYSA-N [1-[2-[1-(2-methylprop-2-enoyloxy)cyclohexyl]ethyl]cyclohexyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1(CCC2(CCCCC2)OC(=O)C(C)=C)CCCCC1 LZVABRWSXQNGJP-UHFFFAOYSA-N 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
- 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 9
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- 239000003505 polymerization initiator Substances 0.000 description 9
- FUGYGGDSWSUORM-UHFFFAOYSA-N 4-hydroxystyrene Chemical compound OC1=CC=C(C=C)C=C1 FUGYGGDSWSUORM-UHFFFAOYSA-N 0.000 description 8
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 8
- 238000001459 lithography Methods 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
- 238000003756 stirring Methods 0.000 description 8
- 238000009826 distribution Methods 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 6
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000006228 supernatant Substances 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 5
- 239000003112 inhibitor Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- ADJDYDCKLROAKA-UHFFFAOYSA-N 1-[2-(1-hydroxycyclohexyl)ethyl]cyclohexan-1-ol Chemical compound C1CCCCC1(O)CCC1(O)CCCCC1 ADJDYDCKLROAKA-UHFFFAOYSA-N 0.000 description 4
- HXDOZKJGKXYMEW-UHFFFAOYSA-N 4-ethylphenol Chemical compound CCC1=CC=C(O)C=C1 HXDOZKJGKXYMEW-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 238000004817 gas chromatography Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methylcyclopentane Chemical compound CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 4
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 4
- YMAIXWWPLZFJLA-UHFFFAOYSA-N 1-[2-(1-hydroxycyclohexyl)ethynyl]cyclohexan-1-ol Chemical group C1CCCCC1(O)C#CC1(O)CCCCC1 YMAIXWWPLZFJLA-UHFFFAOYSA-N 0.000 description 3
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 3
- IFDUTQGPGFEDHJ-UHFFFAOYSA-N 2-methylprop-2-enoic acid;oxolan-2-one Chemical compound CC(=C)C(O)=O.O=C1CCCO1 IFDUTQGPGFEDHJ-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- CSCPPACGZOOCGX-WFGJKAKNSA-N acetone d6 Chemical compound [2H]C([2H])([2H])C(=O)C([2H])([2H])[2H] CSCPPACGZOOCGX-WFGJKAKNSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000004880 explosion Methods 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 3
- 150000007530 organic bases Chemical class 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 238000007670 refining Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- FKWURGDTWUGDQB-UHFFFAOYSA-N (1-ethylcyclohexyl) prop-2-enoate Chemical compound C=CC(=O)OC1(CC)CCCCC1 FKWURGDTWUGDQB-UHFFFAOYSA-N 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- XLLXMBCBJGATSP-UHFFFAOYSA-N 2-phenylethenol Chemical compound OC=CC1=CC=CC=C1 XLLXMBCBJGATSP-UHFFFAOYSA-N 0.000 description 2
- FFWSICBKRCICMR-UHFFFAOYSA-N 5-methyl-2-hexanone Chemical compound CC(C)CCC(C)=O FFWSICBKRCICMR-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 229920002799 BoPET Polymers 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical class C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- VEBCLRKUSAGCDF-UHFFFAOYSA-N ac1mi23b Chemical compound C1C2C3C(COC(=O)C=C)CCC3C1C(COC(=O)C=C)C2 VEBCLRKUSAGCDF-UHFFFAOYSA-N 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- 150000003973 alkyl amines Chemical group 0.000 description 2
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 238000010538 cationic polymerization reaction Methods 0.000 description 2
- 239000012295 chemical reaction liquid Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 125000004386 diacrylate group Chemical group 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Natural products CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 229940116333 ethyl lactate Drugs 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 2
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 238000000622 liquid--liquid extraction Methods 0.000 description 2
- VHRYZQNGTZXDNX-UHFFFAOYSA-N methacryloyl chloride Chemical compound CC(=C)C(Cl)=O VHRYZQNGTZXDNX-UHFFFAOYSA-N 0.000 description 2
- JESXATFQYMPTNL-UHFFFAOYSA-N mono-hydroxyphenyl-ethylene Natural products OC1=CC=CC=C1C=C JESXATFQYMPTNL-UHFFFAOYSA-N 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000001376 precipitating effect Effects 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 239000007870 radical polymerization initiator Substances 0.000 description 2
- 238000010526 radical polymerization reaction Methods 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 238000003828 vacuum filtration Methods 0.000 description 2
- VSYDNHCEDWYFBX-UHFFFAOYSA-N (1-methylcyclopentyl) 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1(C)CCCC1 VSYDNHCEDWYFBX-UHFFFAOYSA-N 0.000 description 1
- CCAWBBMEUQULSR-UHFFFAOYSA-N (2,5-dimethyl-1-prop-2-enoyloxyhexyl) prop-2-enoate Chemical compound CC(C)CCC(C)C(OC(=O)C=C)OC(=O)C=C CCAWBBMEUQULSR-UHFFFAOYSA-N 0.000 description 1
- VBODKNIRHBYKGV-UHFFFAOYSA-N (2,5-dimethyl-5-prop-2-enoyloxyhexan-2-yl) prop-2-enoate Chemical compound C=CC(=O)OC(C)(C)CCC(C)(C)OC(=O)C=C VBODKNIRHBYKGV-UHFFFAOYSA-N 0.000 description 1
- UVHXEHGUEKARKZ-UHFFFAOYSA-N 1-ethenylanthracene Chemical compound C1=CC=C2C=C3C(C=C)=CC=CC3=CC2=C1 UVHXEHGUEKARKZ-UHFFFAOYSA-N 0.000 description 1
- LIPRQQHINVWJCH-UHFFFAOYSA-N 1-ethoxypropan-2-yl acetate Chemical compound CCOCC(C)OC(C)=O LIPRQQHINVWJCH-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- NJBCRXCAPCODGX-UHFFFAOYSA-N 2-methyl-n-(2-methylpropyl)propan-1-amine Chemical compound CC(C)CNCC(C)C NJBCRXCAPCODGX-UHFFFAOYSA-N 0.000 description 1
- SHDZTIZBSYDZSH-UHFFFAOYSA-N 2-methylprop-2-enoyl bromide Chemical compound CC(=C)C(Br)=O SHDZTIZBSYDZSH-UHFFFAOYSA-N 0.000 description 1
- LPEKGGXMPWTOCB-UHFFFAOYSA-N 8beta-(2,3-epoxy-2-methylbutyryloxy)-14-acetoxytithifolin Natural products COC(=O)C(C)O LPEKGGXMPWTOCB-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
- 125000004054 acenaphthylenyl group Chemical group C1(=CC2=CC=CC3=CC=CC1=C23)* 0.000 description 1
- HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- DJBAOXYQCAKLPH-UHFFFAOYSA-M bis(4-tert-butylphenyl)iodanium;1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate Chemical compound [O-]S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F.C1=CC(C(C)(C)C)=CC=C1[I+]C1=CC=C(C(C)(C)C)C=C1 DJBAOXYQCAKLPH-UHFFFAOYSA-M 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- HXCKCCRKGXHOBK-UHFFFAOYSA-N cycloheptane Chemical compound [CH]1CCCCCC1 HXCKCCRKGXHOBK-UHFFFAOYSA-N 0.000 description 1
- DIOQZVSQGTUSAI-NJFSPNSNSA-N decane Chemical compound CCCCCCCCC[14CH3] DIOQZVSQGTUSAI-NJFSPNSNSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 150000002012 dioxanes Chemical class 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- ODQWQRRAPPTVAG-GZTJUZNOSA-N doxepin Chemical compound C1OC2=CC=CC=C2C(=C/CCN(C)C)/C2=CC=CC=C21 ODQWQRRAPPTVAG-GZTJUZNOSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- BHXIWUJLHYHGSJ-UHFFFAOYSA-N ethyl 3-ethoxypropanoate Chemical compound CCOCCC(=O)OCC BHXIWUJLHYHGSJ-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N hydrochloric acid Substances Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical class I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000000671 immersion lithography Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- ZQMHJBXHRFJKOT-UHFFFAOYSA-N methyl 2-[(1-methoxy-2-methyl-1-oxopropan-2-yl)diazenyl]-2-methylpropanoate Chemical compound COC(=O)C(C)(C)N=NC(C)(C)C(=O)OC ZQMHJBXHRFJKOT-UHFFFAOYSA-N 0.000 description 1
- 229940057867 methyl lactate Drugs 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- IZJVVXCHJIQVOL-UHFFFAOYSA-N nitro(phenyl)methanesulfonic acid Chemical compound OS(=O)(=O)C([N+]([O-])=O)C1=CC=CC=C1 IZJVVXCHJIQVOL-UHFFFAOYSA-N 0.000 description 1
- ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 1
- BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- BJEYNNFDAPPGST-UHFFFAOYSA-N oxirene Chemical compound O1C=C1 BJEYNNFDAPPGST-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- RPDAUEIUDPHABB-UHFFFAOYSA-N potassium ethoxide Chemical compound [K+].CC[O-] RPDAUEIUDPHABB-UHFFFAOYSA-N 0.000 description 1
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- CBMSDILKECEMOT-UHFFFAOYSA-N potassium;2-methylpropan-1-olate Chemical compound [K+].CC(C)C[O-] CBMSDILKECEMOT-UHFFFAOYSA-N 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- VWQXLMJSFGLQIT-UHFFFAOYSA-N prop-2-enoyl bromide Chemical compound BrC(=O)C=C VWQXLMJSFGLQIT-UHFFFAOYSA-N 0.000 description 1
- ARJOQCYCJMAIFR-UHFFFAOYSA-N prop-2-enoyl prop-2-enoate Chemical compound C=CC(=O)OC(=O)C=C ARJOQCYCJMAIFR-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 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
- 238000001577 simple distillation Methods 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- XHFLOLLMZOTPSM-UHFFFAOYSA-M sodium;hydrogen carbonate;hydrate Chemical class [OH-].[Na+].OC(O)=O XHFLOLLMZOTPSM-UHFFFAOYSA-M 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- XBFJAVXCNXDMBH-UHFFFAOYSA-N tetracyclo[6.2.1.1(3,6).0(2,7)]dodec-4-ene Chemical compound C1C(C23)C=CC1C3C1CC2CC1 XBFJAVXCNXDMBH-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-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
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/608—Esters of carboxylic acids having a carboxyl group bound to an acyclic carbon atom and having a ring other than a six-membered aromatic ring in the acid moiety
-
- 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
- C08F22/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
- C08F22/10—Esters
- C08F22/1006—Esters of polyhydric alcohols or polyhydric phenols, e.g. ethylene glycol dimethacrylate
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/013—Esters of alcohols having the esterified hydroxy group bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
- C07C69/533—Monocarboxylic acid esters having only one carbon-to-carbon double bond
- C07C69/54—Acrylic acid esters; Methacrylic acid esters
-
- 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
- C08F122/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
- C08F122/10—Esters
-
- 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
- C08F22/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
- C08F22/10—Esters
-
- 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
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
-
- 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
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
- C08F222/1006—Esters of polyhydric alcohols or polyhydric phenols
- C08F222/102—Esters of polyhydric alcohols or polyhydric phenols of dialcohols, e.g. ethylene glycol di(meth)acrylate or 1,4-butanediol dimethacrylate
-
- 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
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
-
- 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
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/08—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated side groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur, or oxygen atoms in addition to the carboxy oxygen
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Materials For Photolithography (AREA)
Abstract
Description
本發明係關於有用於以阻劑為代表之半導體微影術用樹脂、黏著劑、接著劑、油墨、塗料、薄膜等之製造的新穎之二官能(甲基)丙烯酸酯化合物、其聚合物,又,係關於含有該聚合物之阻劑用樹脂組成物,及含有該二官能(甲基)丙烯酸酯化合物之硬化性組成物及其硬化物。
於微影術中,伴隨積體度之增大,係要求型成更微細之圖型,目前係量產使用以KrF準分子雷射光(波長248nm)或ArF準分子雷射光(波長193nm)所進行的微影術技術。又,據稱藉由組合準分子雷射與液浸微影術技術,可進行50nm左右以下之等級的微細加工。再者關於以波長短的F2準分子雷射光(波長157nm),或較此等準分子雷射更短波長之EUV(極紫外線)或X射線,還有以電子束所進行的微影術技術亦有進行研究開發。
作為如此的高解像度微影術材料之一,係有化學增強型阻劑。作為化學增強型阻劑之基材的聚合物,包含具有經可藉由酸的作用脫離之酸解離性基保護極性基之結構的構成單位,於曝光部中,藉由自光酸產生劑所產生之酸的作用,使酸解離性基脫離,聚合物之極性產生變化,在曝光部與未曝光部對顯影液之溶解性產生差異,藉此可形成圖型。
如此的化學增強型阻劑用聚合物之合成所使用的單體,係使用具有將羥基苯乙烯之羥基以酸解離性基保護之結構的化合物,或具有將丙烯酸或甲基丙烯酸(以下表示為(甲基)丙烯酸)之羧基以酸解離性基保護之結構的化合物。特別是使用ArF準分子雷射之微影術中,係適合地使用於波長193nm之透過性良好的酸解離性之(甲基)丙烯酸酯。
專利文獻1中,揭示藉由使用羧基之氫原子被酸解離性之交聯基取代的多官能(甲基)丙烯酸酯作為共單體,對聚合物導入交聯結構,對顯影對比或耐蝕刻性能的提高為有利。但是,專利文獻1所例示者僅為2,5‐二甲基己二醇二丙烯酸酯等鏈狀之二醇或三醇之二或三酯,賦予感度、解像性及蝕刻耐性更優良的阻劑用樹脂之新穎單體受到需求。
[先前技術文獻]
[專利文獻]
[專利文獻1]日本特開2002-148816號公報
[發明所欲解決之課題]
本發明之課題,係提供感度、解像性、蝕刻耐性優良的阻劑用聚合物及賦予該聚合物之新穎單體化合物。
[用以解決課題之手段]
本發明者等人為了解決上述課題而深入研究的結果,發現具有特定結構之化合物,可解決其課題,而完成本發明。
又,本發明為使用上述化合物作為單體的聚合物、含有該聚合物之阻劑用樹脂組成物。
進一步地,本發明為含有上述化合物之硬化性組成物及其硬化物。
又進一步地,本發明為含有上述化合物之交聯劑、以含有前述交聯劑與結構中具有乙烯性雙鍵之樹脂為特徵的硬化性樹脂組成物,及使前述硬化性樹脂組成物硬化而得到之硬化物。
[發明之效果]
依照使用本發明之(甲基)丙烯酸酯之聚合物,可賦予感度、解像性、蝕刻耐性優良的阻劑用樹脂。
本發明之化合物,為以下之式(1)表示者。
此處,式(1)中,R1
表示氫原子或甲基。R2
表示碳數1~6之脂肪族烴基,較佳為甲基、乙基、異丙基、t-丁基。m表示0~5之整數,較佳為0~2之整數。n表示0~4之整數,較佳為1~3之整數。
式(1)表示之化合物之具體例子,可列舉例如1,2-雙-[(1-丙烯醯氧基)環氧雜環丁烷基]乙烷、1,2-雙-[(1-丙烯醯氧基)環戊基]乙烷、1,2-雙-[(1-丙烯醯氧基)環己基]乙烷、1,2-雙-[(1-丙烯醯氧基)環庚基]乙烷、1,2-雙-[(1-丙烯醯氧基)環辛基]乙烷、1,2-雙-[(1-甲基丙烯醯氧基)環氧雜環丁烷基]乙烷、1,2-雙-[(1-甲基丙烯醯氧基)環戊基]乙烷、1,2-雙-[(1-甲基丙烯醯氧基)環己基]乙烷、1,2-雙-[(1-甲基丙烯醯氧基)環庚基]乙烷、1,2-雙-[(1-甲基丙烯醯氧基)環辛基]乙烷等。
上述反應所用之鹼觸媒並無特殊限定,可由金屬鈉或金屬鉀等之鹼金屬;氫氧化鈉、氫氧化鉀、氫氧化鋰等之鹼金屬氫氧化物;或鉀甲醇化物、鉀乙醇化物、鉀異丁醇化物、鉀-t-丁醇化物、鈉甲醇化物、鈉乙醇化物等之鹼金屬醇化物中選擇。此等之中尤較佳為鹼金屬氫氧化物。
上述反應中之鹼觸媒的使用量並無特殊限定,相對於式(2)之酮1莫耳而言為0.1~20莫耳、較佳為0.5~10莫耳。
上述反應所用之溶劑並無特殊限定,可使用飽和脂肪族烴、芳香族烴、脂肪族醚、非質子性極性溶劑。此等之中尤較佳為飽和脂肪族烴,例如可列舉己烷、庚烷、辛烷、壬烷、癸烷、環戊烷、環己烷、甲基環戊烷、甲基環己烷、十氫萘等。此等之中尤特佳為己烷、環己烷、甲基環戊烷、甲基環己烷。
上述反應中之溶劑的使用量並無特殊限定,係式(2)之酮的重量之2~20倍量,較佳為2~10倍量。
上述反應具體而言,係於不鏽鋼製等之耐壓反應容器中,置入鹼金屬化合物、脂肪族烴溶劑,與式(2)表示之環式酮化合物,以氮氣將耐壓反應容器內進行取代後,將反應容器密封,一邊壓入乙炔,一邊昇溫與式(2)表示之環式酮化合物反應。反應溫度並無特殊限定,係0~100℃、較佳為10~60℃。反應壓力並無特殊限定,以乙炔分壓計算,通常係0~1MPa(計示壓力)、較佳為0~0.2MPa(計示壓力)。乙炔分壓越高,反應速度越快,但乙炔容易引起分解爆炸,因此為了防止分解爆炸,較佳僅可能降低乙炔分壓。再者,為了防止分解爆炸,亦可導入氮、氬、丙烷等之惰性氣體,將乙炔稀釋來進行反應。反應時間雖依反應溫度或乙炔分壓等其他條件而異,批式的情況時,通常係0.5~20小時、較佳為1~8小時。再者,該反應只要於乙炔之吸收成為零之時結束即可。
上述反應後,亦可依需要進行洗淨處理、萃取處理、精製處理、乾燥處理。
接著,將該式(3)表示之化合物氫化。
氫化反應並無特殊限定,例如,係藉由在氫化觸媒之存在下,使用飽和脂肪族烴、芳香族烴、脂肪族醇、脂肪族醚等之溶劑,使式(3)之化合物與氫接觸來進行。
上述氫化反應所用之氫化觸媒並無特殊限定,例如使用鎳、鈀、釕、銠、鉑等之金屬觸媒,此等金屬觸媒通常係作為載持於碳、二氧化矽、氧化鋁、二氧化矽氧化鋁、氧化鎂等之載體的金屬載持氫化觸媒來使用。金屬載持氫化觸媒,例如可列舉Pd/C等。金屬之載持量並無特殊限定,較佳為0.3~10重量%。又,如此的金屬載持氫化觸媒可使用市售者。
上述氫化反應中之金屬觸媒之使用量並無特殊限定,例如相對於式(3)之化合物而言,以金屬量計算,係0.001~1重量%之範圍,較佳為0.05~0.5重量%。
上述氫化反應之條件並無特殊限定。氫化反應亦可由玻璃製之反應容器進行。此時,氫壓可為常壓附近、溫度亦可為室溫附近。該氫化反應時,若使用氣體量管導入氫,則可定量氫的消耗量。氫化反應之反應時間並無特殊限定,例如係1~20小時、較佳為2~10小時。又,氫化時使用耐壓容器時,氫壓係0.3~15MPa、較佳為0.5~10MPa,反應溫度係10~150℃、較佳為20~100℃,反應時間係1~20小時、較佳為2~10小時。
上述反應後,亦可依需要進行洗淨處理、萃取處理、精製處理、乾燥處理。
接著,將該式(4)表示之二醇化合物予以(甲基)丙烯酸酯化。式(4)表示之二醇化合物之(甲基)丙烯酸酯化可藉由公知方法進行,例如係有於酸觸媒存在下使二醇與(甲基)丙烯酸反應之通常的酯化反應、使用其他(甲基)丙烯酸酯之酯交換反應、與(甲基)丙烯酸酐反應之方法,或者在有機鹼存在下使(甲基)丙烯酸鹵化物進行反應的方法等。
上述反應所用之(甲基)丙烯酸鹵化物並無特殊限定,例如可列舉丙烯酸氯化物、丙烯酸溴化物、甲基丙烯酸氯化物、甲基丙烯酸溴化物等。
上述反應中之(甲基)丙烯酸鹵化物之量並無特殊限定,相對於式(4)表示之二醇化合物而言為1.0~10倍當量、較佳為1.2~5倍當量。
上述反應所用之有機鹼,較佳為有機胺,例如可列舉甲胺、二甲胺、三甲胺、乙胺、二乙胺、三乙胺、n-丙胺、二-n-丙胺、二異丙胺、三-n-丙胺、n-丁胺、二-n-丁胺、二異丁胺等之脂肪族胺;苯胺、甲基苯胺、甲苯胺等之芳香族胺;吡啶、吡咯、哌啶等之雜環式胺。
上述反應中之有機鹼之量並無特殊限定,相對於(甲基)丙烯酸鹵化物而言為1.0~10倍當量、較佳為1.2~5倍當量。
上述反應所用之溶劑並無特殊限制。溶劑例如可使用甲苯、二甲苯等之芳香族烴溶劑;己烷、庚烷等之脂肪族烴溶劑;二乙基醚、四氫呋喃、單乙二醇二甲基醚、二乙二醇二甲基醚等之醚系溶劑;丙酮、甲基乙基酮、甲基異丁基酮等之酮系溶劑;乙腈、苯甲腈等之腈溶劑;乙酸乙酯、乙酸丁酯、伽瑪丁內酯等之酯系溶劑;二甲基甲醯胺或二甲基乙醯胺、N-甲基吡咯啶酮等之醯胺系溶劑等。
上述反應中之反應溫度並無特殊限定,係 -20~80℃、較佳為-10℃~30℃。
上述反應後,亦可依需要進行洗淨處理、萃取處理、精製處理、乾燥處理。
藉由以上說明之製造方法,可得到本發明之式(1)表示之化合物。可否製造該化合物,可藉由NMR等之公知方法確認。
本發明之式(1)表示之化合物,可使其單獨,或與可與式(1)表示之化合物共聚合之單體反應,得到具有源自該化合物之構成單位的聚合物。如此的單體,可列舉具有乙烯性雙鍵之單體,其結構並無特殊限定,例如可列舉苯乙烯系單體、(甲基)丙烯酸酯系單體、降莰烯系單體等。苯乙烯系單體,係指具有類似苯乙烯之骨架的單體,例如可列舉苯乙烯、乙烯基萘、乙烯基蒽、羥基苯乙烯等,及對此等附加各種取代基之衍生物。(甲基)丙烯酸酯系單體,係指具有類似(甲基)丙烯酸之骨架的單體,可列舉丙烯酸、甲基丙烯酸,或由該等所衍生之各種(甲基)丙烯酸酯。降莰烯系單體,係指具有類似降莰烯之骨架的單體,可列舉降莰烯、三環癸烯、四環十二烯等,及對此等附加各種取代基之衍生物。又,茚、苊烯等亦能夠共聚合。又,將本發明之聚合物用於阻劑用途時,為了調整對微影術溶劑或鹼顯影液之溶解性或基板密合性等,亦可使用公知之阻劑樹脂所使用的各種具有乙烯雙鍵之單體,作為上述單體。
上述聚合反應可採用公知之自由基聚合、陽離子聚合,或陰離子聚合。各自之聚合反應的條件並無限定,例如自由基聚合的情況時,係在偶氮系聚合起始劑或過氧化物系聚合起始劑之存在下,於40~160℃、特佳為60~120℃進行反應。較佳為使用溶劑,較佳為依單體或自由基聚合起始劑、所生成之聚合物種類,來選擇將此等充分溶解的溶劑。
該聚合物例如可使用於半導體微影術所必要的阻劑等之用途。該聚合物特佳為使用於含有其之阻劑用樹脂組成物。該阻劑用樹脂組成物中,除了聚合物外,且含有酸產生劑、酸擴散抑制劑、以及將此等均勻溶解的塗膜形成用溶劑等。
酸產生劑,可由至今為止作為化學增強型阻劑用之酸產生劑而提案者中適當選擇來使用。如此的例子,可列舉錪鹽或鋶鹽等之鎓鹽、肟磺酸酯類、雙烷基或雙芳基磺醯基重氮甲烷類等之重氮甲烷類、硝基苯甲基磺酸酯類、亞胺基磺酸酯類、二碸類等,其中尤以鎓鹽為佳。此等可單獨使用、亦可組合2種以上使用。相對於本發明之聚合物100質量份而言,通常以0.5~30質量份、較佳以1~10質量份之範圍使用酸產生劑。
酸擴散抑制劑,可由至今為止作為化學增強型阻劑用之酸擴散抑制劑所提案者中適當選擇。如此的例子,可列舉含氮有機化合物,較佳為一級~三級之烷胺或羥基烷胺。特佳為三級烷胺、三級羥基烷胺,其中尤以三乙醇胺、三異丙醇胺特佳。此等可單獨使用、亦可組合2種以上使用。相對於本發明之聚合物100重量份而言,通常係以0.01~5.0質量份之範圍使用酸擴散抑制劑。
塗膜形成用溶劑,只要係可溶解構成阻劑用樹脂組成物之各成分,而成為均勻溶液者即可,可由作為塗膜形成用溶劑所公知者中使用任意之1種單獨溶劑或2種以上之混合溶劑。由於溶解性優良,較佳為具有由酮鍵、酯鍵、醚鍵,及羥基中選出的至少1種以上之極性基的溶劑。其中尤以在常壓下的沸點為110~220℃之溶劑,由於在旋轉塗佈後之烘烤中蒸發速度為適度,製膜性優良,故為特佳。如此溶劑之具體例子,可列舉甲基異丁基酮、甲基異戊基酮、甲基戊基酮、環己酮等之具有酮鍵之溶劑;丙二醇單甲基醚(PGME)、丙二醇單乙基醚等之具有醚鍵與羥基之溶劑;丙二醇單甲基醚乙酸酯(PGMEA)、丙二醇單乙基醚乙酸酯、3-乙氧基丙酸乙酯等之具有醚鍵與酯鍵之溶劑;乳酸甲酯、乳酸乙酯等之具有酯鍵與羥基之溶劑;γ-丁內酯等之具有酯鍵之溶劑等。其中尤以PGMEA、PGME、γ-丁內酯、乳酸乙酯為佳。
阻劑用樹脂組成物中,可進一步依期望,依需要適當含有以防止酸產生劑之感度劣化或提高阻劑圖型之形狀、曝光後安定性等為目的之有機羧酸類或磷之含氧酸類、用以改良阻劑膜之性能的附加樹脂、用以提高塗佈性之界面活性劑、溶解抑制劑、可塑劑、安定劑、著色劑、暈光防止劑、染料等作為阻劑用添加劑所慣用之化合物。
又,本發明之式(1)表示之化合物,與已知之(甲基)丙烯酸酯同樣地,可作為硬化性組成物之原料使用。硬化性組成物中可含有其他之(甲基)丙烯酸酯或具有可聚合之乙烯性雙鍵的其他化合物,及聚合起始劑等。聚合起始劑並無特殊限定,例如可列舉光(或熱)自由基聚合起始劑、光(或熱)陽離子聚合起始劑、光(或熱)陰離子聚合起始劑等。此等聚合起始劑可使用市售者。
進一步地,本發明之式(1)表示之化合物,由於具有2個乙烯性雙鍵,故可作為交聯劑使用。
使用本發明之式(1)表示之化合物作為交聯劑時,可藉由組合含有於側鏈具有乙烯基或(甲基)丙烯醯基之樹脂,或不飽和聚酯、乙烯基酯樹脂等於結構中具有乙烯性雙鍵之樹脂,而作為硬化性樹脂組成物。
上述硬化性組成物及硬化性樹脂組成物係遵照一般方法硬化藉以成為硬化物。硬化物之形狀並無特殊限定,例如可列舉膜、成型體等。
[實施例]
以下列舉實施例以詳細說明本發明,但本發明不受此等實施例任何限定。
本實施例中之合成物的鑑定,係藉由1
H-NMR及13
C-NMR進行。又,純度、產率係藉由氣相層析求得。
實施例1
1,2-雙-[(1-甲基丙烯醯氧基)環己基]乙烷之合成:
(1)1,2-雙[(1-羥基)環己基]乙炔之合成
於30L熱壓釜中給入氫氧化鉀1,599g、環己酮1,401g、甲基環己烷12.0kg。將反應容器內以氮取代後,進行乙炔取代。之後,於反應溫度30℃、乙炔壓(計示壓力)0.04MPa以下進行反應,於乙炔的吸收成為零的4小時結束反應。對反應容器內添加21kg離子交換水進行1小時攪拌,將所生成的固體成分使用加壓過濾器分離。
接著,將所得之固體成分置入10L玻璃容器,投入5kg離子交換水,室溫下攪拌30分鐘後,以加壓過濾器將固體成分分離。重複進行該操作至濾液之pH成為7為止。將所得之固體物於40℃減壓乾燥29小時。將該乾燥固體760g予以減壓簡單蒸餾(2.7kPa、115℃、3小時),進行去除未反應成分等輕質成分。所得之重質成分(底部殘渣)為730g,GC分析的結果,1,2-雙[(1-羥基)環己基]乙炔之純度為98.6%。13
C-NMR(400MHz、CD3
OD):σppm=24.5、26.4、41.0、69.1、88.8
(2)1,2-雙[(1-羥基)環己基]乙烷之合成(氫化)
於具備500cc氣體量管(連接於氮管線或氫管線)、攪拌機、溫度計、三通旋塞(連接於排氣管線或隔膜泵)之1L四口燒瓶中,投入(1)所得到之1,2-雙[(1-羥基)環己基]乙炔50.0g、甲醇400g,以20℃水浴攪拌並溶解。重複以隔膜泵將系內減壓,之後以氮恢復壓力,將含有氣體量管之系內以氮進行取代。接著,添加10%Pd/C(和光純藥製)1.05g作為觸媒,使用甲醇50g將系內充分洗淨。將連接於氣體量管之氣體切換為氫管線,與氮取代時同樣地將系內以氫進行取代。填充氫至氣體量管之水位顯示500cc的刻度為止,於20~22℃下攪拌4.5小時進行氫化反應。途中,重複反應之進行,亦即伴隨氫的消耗使氣體量管之水位上昇,而於水位之刻度成為0cc時再度填充氫至水位之刻度成為500cc為止的動作,來測量氫的消耗量。以薄層層析確認反應結束,氫的消耗量為較理論量稍多的10.6L(可認為一部分漏至系外)。反應結束後,將系內以氮進行取代後將觸媒藉由過濾分離。將濾液於30℃、2kPa~0.2kPa濃縮乾燥,得到淡灰白色之粗結晶51.0g。
對該粗結晶添加四氫呋喃160ml,將內溫昇溫至47℃使其完全溶解。接著慢慢降低溫度,冷卻至4℃使結晶充分析出後,於-25℃之冷凍庫保管一晩。翌日藉由過濾而濾離結晶,於30℃、0.2kPa減壓乾燥,得到淡灰白色之結晶44.1g。將結晶藉由NMR分析,確認其係1,2-雙[(1-羥基)環己基]乙烷。
13
C-NMR(400MHz、CD3
OD):δppm=23.3、27.1、35.9、38.3、72.0
又,GC分析之結果,純度為99.6%、產率為87.4%。
(3)1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷之合成
對具備攪拌機、溫度計、附側管之滴液漏斗的1L四口燒瓶,於純空氣氣流下投入(2)所得到之1,2-雙[(1-羥基)環己基]乙烷42.9g(0.19莫耳)、乙腈337g、三乙胺69.0g(0.68莫耳)。此時,1,2-雙[(1-羥基)環己基]乙烷未溶解。以冰浴進行冷卻,於10℃以下花費80分鐘滴下甲基丙烯酸氯化物59.4g(0.57莫耳)。滴下結束後,於20℃進一步反應14小時。接著,以冰浴冷卻反應液,於5℃以下花費30分鐘滴下甲醇34.0g,滴下結束後於20℃持續3小時攪拌。
對該反應液添加乙酸乙酯230.8g與離子交換水128.7g,進行液液萃取操作。對水層添加乙酸乙酯115.8g,進一步進行液液萃取操作。將所得之有機層合併,依次以1N-鹽酸128.7g、接著飽和碳酸氫鈉水132.3g、最後飽和食鹽水149g進行洗淨。將有機層以無水硫酸鈉脫水,過濾後,將濾液於30℃減壓濃縮,得到褐色之粗結晶84.2g。將該粗結晶溶解於乙酸乙酯,以庚烷~庚烷:乙酸乙酯=100:1為溶離液,以二氧化矽凝膠管柱精製後,濃縮而得到黃色結晶。將該黃色結晶再度溶解於乙酸乙酯300ml,使用活性碳5.0g脫色。將活性碳過濾後,將濾液減壓乾燥,得到微黃色結晶49.1g。將微黃色結晶藉由NMR分析,確認其係1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷。
1
H-NMR(400MHz、acetone-d6):δppm=1.23-1.62 (16H)、1.90(6H)、1.94(4H)、2.23(4H)、5.53(2H)、6.00 (2H)13
C-NMR(400MHz、acetone-d6):δppm=18.6、22.6、26.2、31.2、35.2、83.9、124.3、139.0、166.4
又,GC分析之結果,純度為99.4%。
實施例2
γ-丁內酯甲基丙烯酸酯/甲基丙烯酸1-甲基-1-環戊酯/1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷共聚物之合成:
對具備Dimroth冷卻管、溫度計、滴液漏斗之300mL三口燒瓶,加入甲基乙基酮(以下稱MEK)37.3g,昇溫至80℃。以等速花費10分鐘滴下將二甲基-2,2’-偶氮雙異丁酸酯(以下稱MAIB)0.35g溶解於MEK 5g之聚合起始劑溶液,之後,持續攪拌10分鐘攪拌。隨後以等速花費180分鐘滴下將MAIB 3.11g、γ-丁內酯甲基丙烯酸酯24.45g、甲基丙烯酸1-甲基-1-環戊酯23.87g,及實施例1所得到之1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷5.22g溶解於MEK 62.9g之單體溶液,滴下結束後進一步於80℃進行180分鐘聚合反應,之後冷卻至室溫。
將所得之聚合液150g,花費5分鐘滴下於甲醇450g與離子交換水150g之混合溶液中,直接持續攪拌30分鐘使樹脂沈澱。重複2次之以減壓過濾濾離樹脂,對所回收之樹脂進一步添加甲醇300g,於室溫攪拌30分鐘洗淨樹脂的操作。將以減壓過濾所濾離的樹脂以MEK 75g溶解後,移至1L茄型燒瓶,添加丙二醇單甲基醚乙酸酯(以下稱PGMEA)450g,於40℃減壓濃縮至內容物成為200g為止,得到共聚物之PGMEA溶液。
藉由加熱殘餘成分求出所得之PGMEA溶液中的共聚物濃度,結果為21.4wt%。共聚物之重量平均分子量(Mw)及分子量分布(Mw/Mn)係以GPC-RI求得,單體組成比係以13
C-NMR求得。各分析條件如以下所示。
<共聚物分析條件>
GPC-RI:示差折射率檢測器、Shodex(註冊商標)管柱LF-804×3支、溶離液THF13
C-NMR:400MHz、丙酮-d6、乙醯丙酮Cr(III)、反向閘控去偶合(inverse gated decoupling)法
共聚物之重量平均分子量(Mw)及分子量分布(Mw/Mn)係Mw=17,200、Mw/Mn=3.34。又,共聚物之單體組成比係γ-丁內酯甲基丙烯酸酯/甲基丙烯酸1-甲基-1-環戊酯/1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷為47.8/47.7/4.5。
實施例3
p-羥基苯乙烯/丙烯酸1-乙基-1-環己酯/1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷共聚物之合成:
於保持為氮環境之反應容器中,給入含有p-羥基苯乙烯25wt%、甲醇22wt%、水10wt%之p-乙基酚溶液100g,與丙烯酸1-乙基-1-環己酯9.16g、實施例1所得到之1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷2.87g、tert-十二烷基硫醇0.22g、MAIB 0.90g,使其溶解。一邊攪拌該溶液一邊以1℃/分鐘由40℃昇溫至80℃,於80℃進行2小時半聚合反應後,冷卻至室溫。
將所得之聚合液滴下至甲苯,使聚合物沈澱,去除上清。接著,將沈澱溶解於丙酮,重複將其以甲苯沈澱,並去除上清的操作2次。將沈澱再溶解於丙酮,對其添加己烷使聚合物再沈澱,去除上清液。將所得的沈澱以減壓乾燥器乾燥,得到固體之共聚物。該共聚物之重量平均分子量(Mw),及分子量分布(Mw/Mn)及單體組成比之分析係與實施例2同樣地進行。
共聚物之重量平均分子量(Mw)及分子量分布(Mw/Mn)係Mw=23,900、Mw/Mn=7.44。又,共聚物之單體組成比係p-羥基苯乙烯/丙烯酸1-乙基-1-環己酯/1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷為81.3/15.5/3.2。
實施例4
p-羥基苯乙烯/丙烯酸1-乙基-1-環己酯/1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷共聚物之合成:
於保持為氮環境之反應容器中,給入含有p-羥基苯乙烯25wt%、甲醇22wt%、水10wt%之p-乙基酚溶液200g,與丙烯酸1-乙基-1-環己酯16.9g、實施例1所得到之1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷5.62g、tert-十二烷基硫醇0.62g、MAIB 1.94g,使其溶解。一邊攪拌該溶液一邊以1℃/分鐘由40℃昇溫至80℃,於80℃進行2小時半聚合反應後,冷卻至室溫。
將所得之聚合液滴下至甲苯,使聚合物沈澱,去除上清。接著,將沈澱溶解於丙酮,重複將其以甲苯沈澱,並去除上清的操作2次。將沈澱再溶解於丙酮,對其添加己烷使聚合物再沈澱,去除上清液。將所得的沈澱以減壓乾燥器乾燥,得到固體之共聚物。該共聚物之重量平均分子量(Mw),及分子量分布(Mw/Mn)及單體組成比之分析係與實施例2同樣地進行。
共聚物之重量平均分子量(Mw)及分子量分布(Mw/Mn)係Mw=36,960、Mw/Mn=3.46。又,共聚物之單體組成比係p-羥基苯乙烯/丙烯酸1-乙基-1-環己酯/1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷為75.8/20.4/3.8。
比較例1
p-羥基苯乙烯/丙烯酸1-乙基-1-環己酯/2,5-二甲基己基二醇二丙烯酸酯共聚物之合成:
除了使用2,5-二甲基己基二醇二丙烯酸酯3.94g以取代1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷5.62g以外,係與實施例4同樣地進行合成與分析。
共聚物之重量平均分子量(Mw)及分子量分布(Mw/Mn)係Mw=33,400、Mw/Mn=3.77。又,共聚物之單體組成比係p-羥基苯乙烯/丙烯酸1-乙基-1-環己酯/2,5-二甲基己基二醇二丙烯酸酯為76.0/20.0/4.0。
實施例5
阻劑組成物之配製:
將實施例4所合成之共聚物100質量份、作為酸產生劑之雙-(4-tert-丁基苯基)錪九氟丁磺酸鹽0.3質量份、界面活性劑(DIC製、F447)0.1質量份溶解於丙二醇單甲基醚乙酸酯,配製聚合物濃度15重量%之溶液後,將所得之溶液以孔徑0.1μm之膜濾器過濾而得到阻劑組成物。
比較例2
阻劑組成物之配製:
除了使用比較例1所合成之共聚物以外,係與實施例5同樣地得到阻劑組成物。
試驗例1
阻劑組成物之評估:
於經100℃之加熱板上實施過六甲基二矽氮烷處理1分鐘的矽基板上,旋轉塗佈實施例5或比較例2所配製之阻劑組成物後,於加熱板上110℃、60秒預烘烤而形成膜厚1.0μm之阻劑層。
接著,使用開啟型機座(open frame)曝光裝置(Litho Tech Japan製、UVES-2000),變化波長248nm光的曝光量而照射10mm×10mm之18發閃光(shot)後,於120℃進行90秒的後烘烤(PEB)處理。接著,使用阻劑顯影速度測定裝置(Litho Tech Japan製、RDA-800)於23℃以2.38%氫氧化四甲基銨水溶液顯影,測定各曝光量之顯影中的阻劑膜厚之變化。
基於所得之數據,製成於經60秒顯影的時間點的殘存膜厚率對曝光量(mJ/cm2
)與初期膜厚作圖的曲線(未圖示)。於該曲線中,於殘膜率曲線之殘膜率10%~70%之範圍畫出近似直線,以殘膜率0%時的曝光量(mJ/cm2
),作為阻劑組成物之感度指標之一的Eth感度。Eth感度係為了使殘膜率為0%的必要曝光量,Eth感度之值越小,表示阻劑組成物之感度越高。Eth感度示於表1。又,算出Rmin(溶解速度之最小值,相當於未曝光部之溶解速度),該等亦示於表1。
本發明之阻劑組成物,較於習知技術,在具有同等之Eth感度的同時,Rmin大幅變小。換言之,本發明之阻劑組成物,未曝光部之膜減少降低,可期待溶解對比的改善。
實施例6
硬化性組成物之配製及硬化物之製作:
對作為反應性單體之丙烯酸四氫呋喃甲酯50質量份,混合實施例1所得到之1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷50質量份、光自由基聚合起始劑(BASF製、Irgacure 379)5質量份,配製硬化性組成物。
於2枚經氟處理過的PET薄膜間,夾入厚度100μm之間隔件以及上述硬化性組成物,以水銀燈之波長365nm光進行照射3000mJ/cm2
。之後,剝離PET薄膜,得到由硬化性樹脂組成物之硬化物所構成之薄膜狀樣品。
比較例3
硬化性組成物之配製及硬化物之製作:
除了使用2,5-二甲基己基二醇二丙烯酸酯(CAS編號188837-15-2)以取代1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷以外,係與實施例6同樣地製作硬化性組成物,使其硬化而得到薄膜狀之樣品。
比較例4
硬化性組成物之配製及硬化物之製作:
除了使用三環癸烷二甲醇二丙烯酸酯(CAS編號42594-17-2)以取代1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷以外,係與實施例6同樣地製作硬化性組成物,使其硬化而得到薄膜狀之樣品。
比較例5
硬化性組成物之配製及硬化物之製作:
除了使用9,9-雙[4-(2-丙烯醯氧基乙氧基)苯基]茀(CAS編號1234827-45-2)以取代1,2-雙[(1-甲基丙烯醯氧基)環己基]乙烷以外,係與實施例6同樣地製作硬化性組成物,使其硬化而得到薄膜狀之樣品。
試驗例2
硬化物之評估:
使用實施例6及比較例3~5所得到之薄膜狀之樣品,以下述條件進行動態黏彈性測定,求得硬化物之玻璃轉移點(Tg)。結果示於表2。
<動態黏彈性測定條件>
裝置 : Seiko Instruments製 DMS6100
試樣片 : 1cm×5cm
溫度範圍: 25~250℃
昇溫速度: 2℃/分鐘
頻率 : 1Hz
應變振幅: 10μm
將使用本發明之二丙烯酸酯的硬化性組成物硬化而得到之實施例6之硬化物,相較於將以往之硬化性組成物硬化而得到之比較例3~5之硬化物,Tg高,耐熱性優良。
[產業上之可利用性]
本發明之式(1)表示之化合物,除了阻劑用樹脂之合成原料以外,可利用作為各種硬化性組成物之原料,又,作為具有乙烯性雙鍵之樹脂的交聯劑。
Claims (8)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2018040907 | 2018-03-07 | ||
JP2018-040907 | 2018-03-07 |
Publications (2)
Publication Number | Publication Date |
---|---|
TW201942101A TW201942101A (zh) | 2019-11-01 |
TWI798372B true TWI798372B (zh) | 2023-04-11 |
Family
ID=67846086
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW108107162A TWI798372B (zh) | 2018-03-07 | 2019-03-05 | 新穎之二官能(甲基)丙烯酸酯化合物及聚合物 |
Country Status (6)
Country | Link |
---|---|
US (2) | US11919850B2 (zh) |
EP (1) | EP3763751A4 (zh) |
JP (1) | JP7119066B2 (zh) |
CN (1) | CN111902437B (zh) |
TW (1) | TWI798372B (zh) |
WO (1) | WO2019171958A1 (zh) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP7119065B2 (ja) * | 2018-03-07 | 2022-08-16 | 丸善石油化学株式会社 | 新規の二官能(メタ)アクリレート化合物および重合物 |
CN112661637A (zh) * | 2020-12-23 | 2021-04-16 | 上海博栋化学科技有限公司 | 由金刚烷酮合成的可降解树脂单体及其制备方法 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013141265A1 (ja) * | 2012-03-23 | 2013-09-26 | Jsr株式会社 | フォトレジスト組成物、レジストパターン形成方法及び重合体 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6253664A (ja) * | 1985-08-30 | 1987-03-09 | 東洋コンタクトレンズ株式会社 | 医用材料 |
JP4694686B2 (ja) | 2000-08-31 | 2011-06-08 | 東京応化工業株式会社 | 半導体素子製造方法 |
JP2002338627A (ja) | 2001-05-22 | 2002-11-27 | Daicel Chem Ind Ltd | フォトレジスト用高分子化合物及び感光性樹脂組成物 |
JP2005283632A (ja) | 2004-03-26 | 2005-10-13 | Fuji Photo Film Co Ltd | 重合性組成物およびネガ型画像記録材料 |
JP5638943B2 (ja) | 2007-03-30 | 2014-12-10 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | 負の光学的分散を有する複屈折ポリマーフィルム |
JP6149656B2 (ja) | 2012-09-28 | 2017-06-21 | Jsr株式会社 | フォトレジスト組成物、レジストパターン形成方法、重合体及び化合物 |
US10324377B2 (en) | 2015-06-15 | 2019-06-18 | Tokyo Ohka Kogyo Co., Ltd. | Resist composition and method of forming resist pattern |
JP6574621B2 (ja) * | 2015-06-15 | 2019-09-11 | 東京応化工業株式会社 | レジスト組成物及びレジストパターン形成方法 |
US20190292463A1 (en) | 2016-06-03 | 2019-09-26 | Jnc Corporation | Polymerizable polar compound, liquid crystal composition, and liquid crystal display element |
JP6769131B2 (ja) * | 2016-06-22 | 2020-10-14 | Dic株式会社 | 重合性化合物及び光学異方体 |
-
2019
- 2019-02-20 EP EP19764523.7A patent/EP3763751A4/en active Pending
- 2019-02-20 WO PCT/JP2019/006341 patent/WO2019171958A1/ja unknown
- 2019-02-20 JP JP2020504910A patent/JP7119066B2/ja active Active
- 2019-02-20 CN CN201980017718.2A patent/CN111902437B/zh active Active
- 2019-02-20 US US16/971,043 patent/US11919850B2/en active Active
- 2019-03-05 TW TW108107162A patent/TWI798372B/zh active
-
2023
- 2023-10-13 US US18/486,499 patent/US20240092724A1/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013141265A1 (ja) * | 2012-03-23 | 2013-09-26 | Jsr株式会社 | フォトレジスト組成物、レジストパターン形成方法及び重合体 |
Also Published As
Publication number | Publication date |
---|---|
EP3763751A1 (en) | 2021-01-13 |
US11919850B2 (en) | 2024-03-05 |
US20200392066A1 (en) | 2020-12-17 |
TW201942101A (zh) | 2019-11-01 |
CN111902437A (zh) | 2020-11-06 |
WO2019171958A1 (ja) | 2019-09-12 |
EP3763751A4 (en) | 2021-11-24 |
US20240092724A1 (en) | 2024-03-21 |
JPWO2019171958A1 (ja) | 2021-03-18 |
JP7119066B2 (ja) | 2022-08-16 |
CN111902437B (zh) | 2022-10-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20130022914A1 (en) | Homoadamantane derivative, method for producing the same and photosensitive materials for photoresist | |
JPWO2008081768A1 (ja) | 脂環構造含有クロロメチルエーテル類、フォトレジスト用重合性モノマーおよびその製造方法 | |
US20240092724A1 (en) | New bifunctional (meth)acrylate compound and polymer | |
JP7119065B2 (ja) | 新規の二官能(メタ)アクリレート化合物および重合物 | |
TWI648270B (zh) | (甲基)丙烯酸酯化合物、(甲基)丙烯酸共聚物及包含此之感光性樹脂組成物 | |
JP6274288B2 (ja) | 化合物および重合体 | |
TW200419309A (en) | Polymer compound, resist composition and dissolution inhibitor agent containing the polymer compound | |
TW583182B (en) | (Meth)acrylic ester, its raw alcohol, its method of preparation, polymer made by polymerization of said (meth)acrylic ester, chemical amplified resist composition, and method for forming pattern | |
JP6201721B2 (ja) | フォトレジスト用感光性樹脂組成物およびそれに用いる(メタ)アクリル共重合体 | |
CN114080404B (zh) | 聚合物及其制造方法以及抗蚀剂用树脂组合物 | |
JP5456365B2 (ja) | 重合体、レジスト組成物、および微細パターンが形成された基板の製造方法 | |
JP4565820B2 (ja) | 6−トリフルオロメチル−2−ビニルオキシ−4−オキサトリシクロ[4.2.1.03,7]ノナン−5−オン、及び高分子化合物 | |
JP2004161827A (ja) | フッ素含有有橋脂環式ラクトン構造をもつ不飽和単量体、その重合体、化学増幅レジスト及びパターン形成方法 | |
JP4166076B2 (ja) | 含フッ素ビニルエーテルおよびそれを使用した含フッ素重合体、ならびに含フッ素重合体を使用したレジスト材料 | |
JP4229392B2 (ja) | オキサシクロペンチル基をもつアクリル又はメタクリル酸エステルの製造方法 | |
CN118139900A (zh) | 聚合物及抗蚀剂用树脂组合物 | |
JP2019184917A (ja) | レジスト組成物 |