JPWO2015041143A1 - 変性ヒドロキシナフタレンノボラック樹脂、変性ヒドロキシナフタレンノボラック樹脂の製造方法、感光性組成物、レジスト材料及び塗膜 - Google Patents
変性ヒドロキシナフタレンノボラック樹脂、変性ヒドロキシナフタレンノボラック樹脂の製造方法、感光性組成物、レジスト材料及び塗膜 Download PDFInfo
- Publication number
- JPWO2015041143A1 JPWO2015041143A1 JP2015537889A JP2015537889A JPWO2015041143A1 JP WO2015041143 A1 JPWO2015041143 A1 JP WO2015041143A1 JP 2015537889 A JP2015537889 A JP 2015537889A JP 2015537889 A JP2015537889 A JP 2015537889A JP WO2015041143 A1 JPWO2015041143 A1 JP WO2015041143A1
- Authority
- JP
- Japan
- Prior art keywords
- group
- hydroxy naphthalene
- resin
- novolak resin
- modified
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 229920003986 novolac Polymers 0.000 title claims abstract description 183
- 229920005989 resin Polymers 0.000 title claims abstract description 181
- 239000011347 resin Substances 0.000 title claims abstract description 181
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical class C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 title claims abstract description 152
- 239000000203 mixture Substances 0.000 title claims abstract description 40
- 239000000463 material Substances 0.000 title claims abstract description 28
- 238000004519 manufacturing process Methods 0.000 title claims description 26
- 238000000576 coating method Methods 0.000 title claims description 19
- 239000011248 coating agent Substances 0.000 title claims description 18
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 52
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 40
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 37
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 36
- 125000002252 acyl group Chemical group 0.000 claims abstract description 35
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 35
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 34
- 125000004665 trialkylsilyl group Chemical group 0.000 claims abstract description 33
- 125000003118 aryl group Chemical group 0.000 claims abstract description 21
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 18
- 125000005843 halogen group Chemical group 0.000 claims abstract description 17
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 16
- -1 hydroxy naphthalene compound Chemical class 0.000 claims description 103
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 50
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 39
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- 239000000539 dimer Substances 0.000 claims description 19
- 239000000178 monomer Substances 0.000 claims description 19
- 238000005259 measurement Methods 0.000 claims description 18
- 239000003960 organic solvent Substances 0.000 claims description 15
- 239000003377 acid catalyst Substances 0.000 claims description 10
- 230000002209 hydrophobic effect Effects 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 6
- 239000012046 mixed solvent Substances 0.000 claims description 6
- DFQICHCWIIJABH-UHFFFAOYSA-N naphthalene-2,7-diol Chemical compound C1=CC(O)=CC2=CC(O)=CC=C21 DFQICHCWIIJABH-UHFFFAOYSA-N 0.000 claims description 4
- 150000004292 cyclic ethers Chemical group 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 2
- 239000003513 alkali Substances 0.000 abstract description 22
- 206010034972 Photosensitivity reaction Diseases 0.000 abstract description 16
- 230000036211 photosensitivity Effects 0.000 abstract description 16
- 238000010521 absorption reaction Methods 0.000 abstract description 15
- 239000000543 intermediate Substances 0.000 description 46
- 239000011572 manganese Substances 0.000 description 31
- 238000006243 chemical reaction Methods 0.000 description 23
- 230000000052 comparative effect Effects 0.000 description 22
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 21
- 229930003836 cresol Natural products 0.000 description 21
- 150000002989 phenols Chemical class 0.000 description 20
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 18
- 150000001875 compounds Chemical class 0.000 description 18
- 239000003795 chemical substances by application Substances 0.000 description 17
- 150000001896 cresols Chemical class 0.000 description 17
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 12
- 229920002120 photoresistant polymer Polymers 0.000 description 12
- 125000006239 protecting group Chemical group 0.000 description 12
- 235000012431 wafers Nutrition 0.000 description 10
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 8
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 8
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 7
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 7
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 238000007405 data analysis Methods 0.000 description 6
- 229920002223 polystyrene Polymers 0.000 description 6
- 229910052710 silicon Inorganic materials 0.000 description 6
- 239000010703 silicon Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 5
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 description 5
- 229930040373 Paraformaldehyde Natural products 0.000 description 5
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000011342 resin composition Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000006467 substitution reaction Methods 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 5
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 4
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 4
- WTQZSMDDRMKJRI-UHFFFAOYSA-N 4-diazoniophenolate Chemical group [O-]C1=CC=C([N+]#N)C=C1 WTQZSMDDRMKJRI-UHFFFAOYSA-N 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 230000018109 developmental process Effects 0.000 description 4
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 4
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 4
- 125000001188 haloalkyl group Chemical group 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229940100630 metacresol Drugs 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 235000006408 oxalic acid Nutrition 0.000 description 4
- 229920002866 paraformaldehyde Polymers 0.000 description 4
- 239000003504 photosensitizing agent Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 3
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 3
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical class CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- BUDQDWGNQVEFAC-UHFFFAOYSA-N Dihydropyran Chemical compound C1COC=CC1 BUDQDWGNQVEFAC-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- XFSBVAOIAHNAPC-WSORPINJSA-N acetylbenzoylaconine Chemical compound O([C@H]1[C@]2(O)C[C@H]3C45[C@@H]6[C@@H]([C@@]([C@H]31)(OC(C)=O)[C@@H](O)[C@@H]2OC)[C@H](OC)C4[C@]([C@@H](C[C@H]5OC)O)(COC)CN6CC)C(=O)C1=CC=CC=C1 XFSBVAOIAHNAPC-WSORPINJSA-N 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 125000001153 fluoro group Chemical group F* 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- QWBBPBRQALCEIZ-UHFFFAOYSA-N 2,3-dimethylphenol Chemical compound CC1=CC=CC(O)=C1C QWBBPBRQALCEIZ-UHFFFAOYSA-N 0.000 description 2
- CPEXFJVZFNYXGU-UHFFFAOYSA-N 2,4,6-trihydroxybenzophenone Chemical compound OC1=CC(O)=CC(O)=C1C(=O)C1=CC=CC=C1 CPEXFJVZFNYXGU-UHFFFAOYSA-N 0.000 description 2
- NKTOLZVEWDHZMU-UHFFFAOYSA-N 2,5-xylenol Chemical compound CC1=CC=C(C)C(O)=C1 NKTOLZVEWDHZMU-UHFFFAOYSA-N 0.000 description 2
- NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 description 2
- IXQGCWUGDFDQMF-UHFFFAOYSA-N 2-Ethylphenol Chemical class CCC1=CC=CC=C1O IXQGCWUGDFDQMF-UHFFFAOYSA-N 0.000 description 2
- GXYCPGOCXLHIAT-UHFFFAOYSA-N 2-cyclohexyl-6-[(3-cyclohexyl-2-hydroxyphenyl)-(2-hydroxyphenyl)methyl]phenol Chemical compound OC1=CC=CC=C1C(C=1C(=C(C2CCCCC2)C=CC=1)O)C1=CC=CC(C2CCCCC2)=C1O GXYCPGOCXLHIAT-UHFFFAOYSA-N 0.000 description 2
- YCOXTKKNXUZSKD-UHFFFAOYSA-N 3,4-xylenol Chemical compound CC1=CC=C(O)C=C1C YCOXTKKNXUZSKD-UHFFFAOYSA-N 0.000 description 2
- TUAMRELNJMMDMT-UHFFFAOYSA-N 3,5-xylenol Chemical compound CC1=CC(C)=CC(O)=C1 TUAMRELNJMMDMT-UHFFFAOYSA-N 0.000 description 2
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- BLYYQDFZPGAAQM-UHFFFAOYSA-N 6-methoxy-1h-pyrimidin-2-one Chemical compound COC1=CC=NC(O)=N1 BLYYQDFZPGAAQM-UHFFFAOYSA-N 0.000 description 2
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- 229920001214 Polysorbate 60 Polymers 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
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- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 2
- 239000004147 Sorbitan trioleate Substances 0.000 description 2
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
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- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
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- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 125000004744 butyloxycarbonyl group Chemical group 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
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- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
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- 208000013469 light sensitivity Diseases 0.000 description 2
- LPEKGGXMPWTOCB-UHFFFAOYSA-N methyl 2-hydroxypropionate Chemical compound COC(=O)C(C)O LPEKGGXMPWTOCB-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
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- 239000012044 organic layer Substances 0.000 description 2
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 description 2
- 238000000206 photolithography Methods 0.000 description 2
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- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 2
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- PZRKPUQWIFJRKZ-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine Chemical compound NC1=NC(N)=C(N)C(N)=N1 PZRKPUQWIFJRKZ-UHFFFAOYSA-N 0.000 description 1
- CSNFMBGHUOSBFU-UHFFFAOYSA-N pyrimidine-2,4,5-triamine Chemical compound NC1=NC=C(N)C(N)=N1 CSNFMBGHUOSBFU-UHFFFAOYSA-N 0.000 description 1
- DNACGYGXUFTEHO-UHFFFAOYSA-N pyrimidine-2,5-diamine Chemical compound NC1=CN=C(N)N=C1 DNACGYGXUFTEHO-UHFFFAOYSA-N 0.000 description 1
- MPNBXFXEMHPGTK-UHFFFAOYSA-N pyrimidine-4,5,6-triamine Chemical compound NC1=NC=NC(N)=C1N MPNBXFXEMHPGTK-UHFFFAOYSA-N 0.000 description 1
- MISVBCMQSJUHMH-UHFFFAOYSA-N pyrimidine-4,6-diamine Chemical compound NC1=CC(N)=NC=N1 MISVBCMQSJUHMH-UHFFFAOYSA-N 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000007261 regionalization Effects 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 239000001589 sorbitan tristearate Substances 0.000 description 1
- 235000011078 sorbitan tristearate Nutrition 0.000 description 1
- 229960004129 sorbitan tristearate Drugs 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 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
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- KCNSDMPZCKLTQP-UHFFFAOYSA-N tetraphenylen-1-ol Chemical compound C12=CC=CC=C2C2=CC=CC=C2C2=CC=CC=C2C2=C1C=CC=C2O KCNSDMPZCKLTQP-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- DWWMSEANWMWMCB-UHFFFAOYSA-N tribromomethylsulfonylbenzene Chemical compound BrC(Br)(Br)S(=O)(=O)C1=CC=CC=C1 DWWMSEANWMWMCB-UHFFFAOYSA-N 0.000 description 1
- HFFLGKNGCAIQMO-UHFFFAOYSA-N trichloroacetaldehyde Chemical compound ClC(Cl)(Cl)C=O HFFLGKNGCAIQMO-UHFFFAOYSA-N 0.000 description 1
- VZUBRRXYUOJBRS-UHFFFAOYSA-N trichloromethylsulfonylbenzene Chemical compound ClC(Cl)(Cl)S(=O)(=O)C1=CC=CC=C1 VZUBRRXYUOJBRS-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229950002929 trinitrophenol Drugs 0.000 description 1
- ZFEAYIKULRXTAR-UHFFFAOYSA-M triphenylsulfanium;chloride Chemical compound [Cl-].C1=CC=CC=C1[S+](C=1C=CC=CC=1)C1=CC=CC=C1 ZFEAYIKULRXTAR-UHFFFAOYSA-M 0.000 description 1
- WLOQLWBIJZDHET-UHFFFAOYSA-N triphenylsulfonium Chemical compound C1=CC=CC=C1[S+](C=1C=CC=CC=1)C1=CC=CC=C1 WLOQLWBIJZDHET-UHFFFAOYSA-N 0.000 description 1
- 239000012953 triphenylsulfonium Substances 0.000 description 1
- FAYMLNNRGCYLSR-UHFFFAOYSA-M triphenylsulfonium triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F.C1=CC=CC=C1[S+](C=1C=CC=CC=1)C1=CC=CC=C1 FAYMLNNRGCYLSR-UHFFFAOYSA-M 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003739 xylenols Chemical class 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Images
Classifications
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/28—Chemically modified polycondensates
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- C—CHEMISTRY; METALLURGY
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D161/00—Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
- C09D161/04—Condensation polymers of aldehydes or ketones with phenols only
- C09D161/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
- C09D161/14—Modified phenol-aldehyde condensates
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- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
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Abstract
Description
で表される構造部位(I)を繰り返し単位とする変性ヒドロキシナフタレンノボラック樹脂であり、樹脂中に存在するR1のうち少なくとも一つが3級アルキル基、アルコキシアルキル基、アシル基、アルコキシカルボニル基、ヘテロ原子含有環状炭化水素基、トリアルキルシリル基の何れかであることを特徴とする変性ヒドロキシナフタレンノボラック樹脂を提供するものである。
で表される構造部位(I)を繰り返し単位とする変性ヒドロキシナフタレンノボラック樹脂であり、樹脂中に存在するR1のうち少なくとも一つが3級アルキル基、アルコキシアルキル基、アシル基、アルコキシカルボニル基、ヘテロ原子含有環状炭化水素基、トリアルキルシリル基の何れかであることを特徴とする。前記構造部位(I)を有することにより、従来困難であった光感度、解像度及びアルカリ現像性と、耐熱性及び耐吸湿性とを兼備する塗膜が得られ、レジスト材料として特に好適に用いることができる変性ヒドロキシナフタレンノボラック樹脂となる。
で表されるモノマー成分を含有していても良い。本発明の変性ヒドロキシナフタレンノボラック樹脂中の、前記(4)に代表されるモノマー成分の合計の含有量は、解像度と耐熱性とに優れる樹脂となることから2質量%以下であることが好ましく、1質量%以下であることがより好ましい。
測定装置:東ソー株式会社製「HLC−8220 GPC」(8.0mmI.D.×300mm)
カラム:昭和電工株式会社製「Shodex KF802」(8.0mmI.D.×300mm)+昭和電工株式会社製「Shodex KF802」(8.0mmI.D.×300mm)+昭和電工株式会社製「Shodex KF803」(8.0mmI.D.×300mm)+昭和電工株式会社製「Shodex KF804」(8.0mmI.D.×300mm)
検出器:RI(示差屈折計)
データ処理:東ソー株式会社製「GPC−8020モデルIIデータ解析バージョン4.30」
測定条件:カラム温度 40℃
展開溶媒 テトラヒドロフラン(THF)
流速 1.0ml/分
試料:樹脂固形分換算で1.0質量%のテトラヒドロフラン溶液をマイクロフィルターでろ過したもの(5μl)。
標準試料:前記「GPC−8020モデルIIデータ解析バージョン4.30」の測定マニュアルに準拠して、分子量が既知の下記の単分散ポリスチレンを用いた。
(単分散ポリスチレン)
東ソー株式会社製「A−500」
東ソー株式会社製「A−2500」
東ソー株式会社製「A−5000」
東ソー株式会社製「F−1」
東ソー株式会社製「F−2」
東ソー株式会社製「F−4」
東ソー株式会社製「F−10」
東ソー株式会社製「F−20」
装置:日本電子株式会社製「JNM−LA300」
溶媒:DMSO−d6
で表される構造部位(I−1)又は(I−2)であることがより好ましい。
測定装置:東ソー株式会社製「HLC−8220 GPC」(8.0mmI.D.×300mm)
カラム:昭和電工株式会社製「Shodex KF802」(8.0mmI.D.×300mm)+昭和電工株式会社製「Shodex KF802」(8.0mmI.D.×300mm)+昭和電工株式会社製「Shodex KF803」(8.0mmI.D.×300mm)+昭和電工株式会社製「Shodex KF804」(8.0mmI.D.×300mm)
検出器:RI(示差屈折計)
データ処理:東ソー株式会社製「GPC−8020モデルIIデータ解析バージョン4.30」
測定条件:カラム温度 40℃
展開溶媒 テトラヒドロフラン(THF)
流速 1.0ml/分
試料:樹脂固形分換算で1.0質量%のテトラヒドロフラン溶液をマイクロフィルターでろ過したもの(5μl)。
標準試料:前記「GPC−8020モデルIIデータ解析バージョン4.30」の測定マニュアルに準拠して、分子量が既知の下記の単分散ポリスチレンを用いた。
東ソー株式会社製「A−500」
東ソー株式会社製「A−2500」
東ソー株式会社製「A−5000」
東ソー株式会社製「F−1」
東ソー株式会社製「F−2」
東ソー株式会社製「F−4」
東ソー株式会社製「F−10」
東ソー株式会社製「F−20」
の何れかで表される化合物(以下「保護基導入剤」と略記する。)とを反応させる方法が挙げられる。
測定装置:東ソー株式会社製「HLC−8220 GPC」(8.0mmI.D.×300mm)
カラム:昭和電工株式会社製「Shodex KF802」(8.0mmI.D.×300mm)+昭和電工株式会社製「Shodex KF802」(8.0mmI.D.×300mm)+昭和電工株式会社製「Shodex KF803」(8.0mmI.D.×300mm)+昭和電工株式会社製「Shodex KF804」(8.0mmI.D.×300mm)
検出器:RI(示差屈折計)
データ処理:東ソー株式会社製「GPC−8020モデルIIデータ解析バージョン4.30」
測定条件:カラム温度 40℃
展開溶媒 テトラヒドロフラン(THF)
流速 1.0ml/分
試料:樹脂固形分換算で1.0質量%のテトラヒドロフラン溶液をマイクロフィルターでろ過したもの(5μl)。
標準試料:前記「GPC−8020モデルIIデータ解析バージョン4.30」の測定マニュアルに準拠して、分子量が既知の下記の単分散ポリスチレンを用いた。
(単分散ポリスチレン)
東ソー株式会社製「A−500」
東ソー株式会社製「A−2500」
東ソー株式会社製「A−5000」
東ソー株式会社製「F−1」
東ソー株式会社製「F−2」
東ソー株式会社製「F−4」
東ソー株式会社製「F−10」
東ソー株式会社製「F−20」
装置:日本電子(株)製「AL−400」
測定モード:SGNNE(NOE消去の1H完全デカップリング法)
溶媒:ジメチルスルホキシド
パルス角度:45°パルス
試料濃度 :30wt%
積算回数 :10000回
日本電子株式会社製の二重収束型質量分析装置「AX505H(FD505H)」を用いて測定した。
温度計、冷却管、撹拌器を取り付けた1Lの4つ口フラスコに、1−ナフトール144g(1.0モル)、メチルイソブチルケトン400g、水96g及び92%パラホルムアルデヒド27.7g(0.85モル)を仕込んだ。続いて攪拌しながら50%濃度に調整したパラトルエンスルホン酸の水溶液4.8gを添加した。反応系内の水の量は1−ナフトール100質量部に対し、69.9質量部である。その後、攪拌しながら80℃まで昇温して2時間反応させた。反応終了後、系内の溶液を分液ロートに移し水層をメチルイソブチルケトン層から分離除去した。次いて洗浄水が中性を示すまで水洗した後、加熱減圧下にてメチルイソブチルケトンを除去し、ヒドロキシナフタレンノボラック中間体(1)147gを得た。ヒドロキシナフタレンノボラック中間体(1)のGPCチャートを図1に示す。GPCで測定されたヒドロキシナフタレンノボラック中間体(1)の数平均分子量(Mn)は1,765、重量平均分子量(Mw)は3,337、多分散度(Mw/Mn)は1.890であり、ヒドロキシナフタレンノボラック中間体(1)中のモノマー成分の含有量は0.49質量%、ダイマー成分の含有量は0.22質量%であった。
温度計、冷却管、分留管、撹拌器を取り付けた1Lの4つ口フラスコに、2,7−ジヒドロキシナフタレン160g(1.0モル)、メチルイソブチルケトン400g、水96g及び92%パラホルムアルデヒド27.7g(0.85モル)を仕込んだ。続いて攪拌しながら50%濃度に調整したパラトルエンスルホン酸の水溶液4.8gを添加した。反応系内の水の量は2,7−ジヒドロキシナフタレン100質量部に対し、62.9質量部である。その後、攪拌しながら80℃まで昇温して2時間反応させた。反応終了後、系内の溶液を分液ロートに移し水層をメチルイソブチルケトン層から分離除去した。次いで洗浄水が中性を示すまで水洗した後、加熱減圧下にてメチルイソブチルケトンを除去し、ヒドロキシナフタレンノボラック中間体(2)165gを得た。ヒドロキシナフタレンノボラック中間体(2)のGPCチャートを図2に示す。GPCで測定されたヒドロキシナフタレンノボラック中間体(2)の数平均分子量(Mn)は1,142、重量平均分子量(Mw)は1,626、多分散度(Mw/Mn)は1.424であり、ヒドロキシナフタレンノボラック中間体(2)中のモノマー成分の含有量は0.61質量%、ダイマー成分の含有量は1.79質量%であった。
冷却管を設置した100mlの2口フラスコに前記製造例1で得たヒドロキシナフタレンノボラック中間体(1)6.1g、ジヒドロピラン1.7gを仕込み、1,3−ジオキソラン30gに溶解させた。35wt%塩酸水溶液0.01gを添加した後、25℃(室温)で4時間反応を行った。反応終了後、25wt%アンモニア水溶液0.1gを添加し、これをイオン交換水100g中に注ぎ、生成物を沈殿させた。沈殿物を80℃、1.3kPaで減圧乾燥し、前記構造式(1)で表される構造部位(I)を繰り返し単位とする変性ヒドロキシナフタレンノボラック樹脂(1)5.9gを得た。変性ヒドロキシナフタレンノボラック樹脂(1)のGPCチャートを図3に、13C−NMRチャート図を図4に示す。GPCで測定された変性ヒドロキシナフタレンノボラック樹脂(1)の数平均分子量(Mn)は1,745、重量平均分子量(Mw)は3,401、多分散度(Mw/Mn)は1.95であった。変性ヒドロキシナフタレンノボラック樹脂(1)中のテトラヒドロピラニル基とフェノール性水酸基との存在比率[(OX)/(OH)]は、23/77であった。前記構造部位(I)の繰り返し数(前記一般式(2)中のnに相当)は、平均で9.46であった。そして、変性ヒドロキシナフタレンノボラック樹脂(1)中のモノマー成分の含有量は0.33質量%、ダイマー成分の含有量は0.64質量%であった。
実施例1においてジヒドロピラン1.7gをエチルビニルエーテル1.4gに変更した以外は実施例1と同様にして前記構造式(1)で表される構造部位(I)を繰り返し単位とする変性ヒドロキシナフタレンノボラック樹脂(2)5.8gを得た。変性ヒドロキシナフタレンノボラック樹脂(2)のGPCチャートを図5に示す。GPCで測定された変性ヒドロキシナフタレンノボラック樹脂(2)の数平均分子量(Mn)は1,789、重量平均分子量(Mw)は3,515、多分散度(Mw/Mn)は1.97であった。変性ヒドロキシナフタレンノボラック樹脂(2)中のエトキシメチル基とフェノール性水酸基との存在比率[(OX)/(OH)]は、35/65であった。前記構造部位(I)の繰り返し数(前記一般式(2)中のnに相当)は、平均で9.46であった。そして、変性ヒドロキシナフタレンノボラック樹脂(2)中のモノマー成分の含有量は0.28質量%、ダイマー成分の含有量は0.66質量%であった。
冷却管を設置した100mlの2口フラスコに前記製造例1で得たヒドロキシナフタレンノボラック中間体(1)6.1g、二炭酸ジ−t−ブチル2.2gを仕込み、1,3−ジオキソラン30gに溶解させた。トリエチルアミン0.1gを添加した後、80℃で4時間反応を行った。反応終了後、反応物をイオン交換水100g中に注ぎ、得られた沈殿物を80℃、1.3kPaで減圧乾燥し、前記構造式(1)で表される構造部位(I)を繰り返し単位とする変性ヒドロキシナフタレンノボラック樹脂(3)6.2gを得た。変性ヒドロキシナフタレンノボラック樹脂(3)のGPCチャートを図6に示す。GPCで測定された変性ヒドロキシナフタレンノボラック樹脂(3)の数平均分子量(Mn)は1,784、重量平均分子量(Mw)は3,487、多分散度(Mw/Mn)は1.95であった。変性ヒドロキシナフタレンノボラック樹脂(3)中のt−ブトキシカルボニル基とフェノール性水酸基との存在比率[(OX)/(OH)]は、27/73であった。前記構造部位(I)の繰り返し数(前記一般式(2)中のnに相当)は、平均で9.46であった。そして、変性ヒドロキシナフタレンノボラック樹脂(2)中のモノマー成分の含有量は0.25質量%、ダイマー成分の含有量は0.63質量%であった。
実施例1においてヒドロキシナフタレンノボラック中間体(1)6.1gをヒドロキシナフタレンノボラック中間体(2)3.3gに変更した以外は実施例1と同様にして前記構造式(1)で表される構造部位(I)を繰り返し単位とする変性ヒドロキシナフタレンノボラック樹脂(4)2.9gを得た。変性ヒドロキシナフタレンノボラック樹脂(4)のGPCチャートを図7に示す。GPCで測定された変性ヒドロキシナフタレンノボラック樹脂(4)の数平均分子量(Mn)は1,110、重量平均分子量(Mw)は1,547、多分散度(Mw/Mn)は1.39であった。変性ヒドロキシナフタレンノボラック樹脂(4)中のテトラヒドロピラニル基とフェノール性水酸基との存在比率[(OX)/(OH)]は、19/81であった。前記構造部位(I)の繰り返し数(前記一般式(2)中のnに相当)は、平均9.46であった。そして、変性ヒドロキシナフタレンノボラック樹脂(4)中のモノマー成分の含有量は0.56質量%、ダイマー成分の含有量は1.72質量%であった。
実施例2においてヒドロキシナフタレンノボラック中間体(1)6.1gをヒドロキシナフタレンノボラック中間体(2)3.3gに変更した以外は実施例2と同様にして前記構造式(1)で表される構造部位(I)を繰り返し単位とする変性ヒドロキシナフタレンノボラック樹脂(5)3.1gを得た。変性ヒドロキシナフタレンノボラック樹脂(5)のGPCチャートを図8に示す。GPCで測定された変性ヒドロキシナフタレンノボラック樹脂(5)の数平均分子量(Mn)は1,134、重量平均分子量(Mw)は1,663、多分散度(Mw/Mn)は1.46であった。変性ヒドロキシナフタレンノボラック樹脂(5)中のエトキシエチル基とフェノール性水酸基との存在比率[(OX)/(OH)]は、24/76であった。前記構造部位(I)の繰り返し数(前記一般式(2)中のnに相当)は、平均で4.70であった。そして、変性ヒドロキシナフタレンノボラック樹脂(5)中のモノマー成分の含有量は0.97質量%、ダイマー成分の含有量は1.64質量%であった。
実施例3においてヒドロキシナフタレンノボラック中間体(1)6.1gをヒドロキシナフタレンノボラック中間体(2)3.3gに変更した以外は実施例3と同様にして前記構造式(1)で表される構造部位(I)を繰り返し単位とする変性ヒドロキシナフタレンノボラック樹脂(6)3.0gを得た。変性ヒドロキシナフタレンノボラック樹脂(6)のGPCチャートを図9に示す。GPCで測定された変性ヒドロキシナフタレンノボラック樹脂(4)の数平均分子量(Mn)は1,173、重量平均分子量(Mw)は1,675、多分散度(Mw/Mn)は1.43であった。変性ヒドロキシナフタレンノボラック樹脂(6)中のt−ブトキシカルボニル基とフェノール性水酸基との存在比率[(OX)/(OH)]は、26/74であった。前記構造部位(I)の繰り返し数(前記一般式(2)中のnに相当)は、平均で4.70であった。そして、変性ヒドロキシナフタレンノボラック樹脂(6)中のモノマー成分の含有量は0.84質量%、ダイマー成分の含有量は1.73質量%であった。
攪拌機、温度計を備えた2Lの4つ口フラスコに、m−クレゾール648g(6モル)、p−クレゾール432g(4モル)、シュウ酸2.5g(0.2モル)、42%ホルムアルデヒド492gを仕込み、100℃まで昇温させて反応させた。常圧で200℃まで昇温させて脱水蒸留し、230℃で6時間減圧蒸留を行い、比較対照用クレゾールノボラック中間体(1’)736gを得た。比較対照用クレゾールノボラック中間体(1’)のGPCチャートを図10に示す。GPCで測定された比較対照用クレゾールノボラック中間体(1’)の数平均分子量(Mn)は1,450、重量平均分子量(Mw)は10,316、多分散度(Mw/Mn)は7.12であった。また、比較対照用クレゾールノボラック中間体(1’)中のモノマー成分の含有量は0.12質量%、ダイマー成分の含有量は5.86質量%であった。
実施例1においてヒドロキシナフタレンノボラック中間体(1)6.1gを製造例3で得た比較対照用クレゾールノボラック中間体(1’)4.6gに変更した以外は実施例1と同様にして比較対照用変性クレゾールノボラック樹脂(1’)4.6gを得た。GPCで測定された比較対照用変性クレゾールノボラック樹脂(1’)の数平均分子量(Mn)は1,513、重量平均分子量(Mw)は10,758、多分散度(Mw/Mn)は7.11であった。比較対照用変性クレゾールノボラック樹脂(1’)中のテトラヒドロピラニル基とフェノール性水酸基との存在比率[(OX)/(OH)]は、47/53であった。また、比較対照用変性クレゾールノボラック樹脂(1’)中のモノマー成分の含有量は0.15質量%、ダイマー成分の含有量は6.08質量%であった。
実施例2においてヒドロキシナフタレンノボラック中間体(1)6.1gを比較対照用クレゾールノボラック中間体(1’)4.6gに変更した以外は実施例2と同様にして比較対照用変性クレゾールノボラック樹脂(2’)5.0gを得た。GPCで測定された比較対照用変性クレゾールノボラック樹脂(2’)の数平均分子量(Mn)は1,816、重量平均分子量(Mw)は11,929、多分散度(Mw/Mn)は6.57であった。比較対照用変性クレゾールノボラック樹脂(2’)中のエトキシエチル基とフェノール性水酸基との存在比率[(OX)/(OH)]は、47/53であった。また、比較対照用変性クレゾールノボラック樹脂(2’)中のモノマー成分の含有量は0.26質量%、ダイマー成分の含有量は5.39質量%であった。
実施例3においてヒドロキシナフタレンノボラック中間体(1)6.1gを比較対照用クレゾールノボラック中間体(1’)4.6gに変更した以外は実施例3と同様にして比較対照用変性クレゾールノボラック樹脂(3’)5.0gを得た。GPCで測定された比較対照用変性クレゾールノボラック樹脂(3’)の数平均分子量(Mn)は1,810、重量平均分子量(Mw)は11,862、多分散度(Mw/Mn)は6.55であった。比較対照用変性クレゾールノボラック樹脂(6’)中のt−ブトキシカルボニル基とフェノール性水酸基との存在比率[(OX)/(OH)]は、47/53であった。また、比較対照用変性クレゾールノボラック樹脂(3’)中のモノマー成分の含有量は0.20質量%、ダイマー成分の含有量は5.28質量%であった。
変性ヒドロキシナフタレンノボラック樹脂(1)〜(6)及び比較対照用変性クレゾールノボラック樹脂(1’)〜(3’)のそれぞれについて、以下の要領で各種評価試験を行った。結果を表1、2に示す。
変性ヒドロキシナフタレンノボラック樹脂又は比較対照用変性クレゾールノボラック樹脂19部、光酸発生剤[和光純薬株式会社製「WPAG−336」ジフェニル(4−メチルフェニル)スルフォニウムトリフルオロメタンスルフォネート)]1部、及びプロピレングリコールモノメチルエーテルアセテート80部を混合したものを、0.2μmメンブランフィルターを用いて濾過し、感光性組成物(1)〜(6)及び比較対照用感光性組成物(1’)〜(3’)を得た。
前記感光性組成物又は比較対照用感光性組成物を5インチシリコンウェハー上に約1μmの厚さになるようにスピンコーターで塗布し、110℃のホットプレート上で60秒乾燥させた。このウェハーを2枚用意し、一方を「露光なしサンプル」とし、他方を「露光有サンプル」としてhi線ランプ(ウシオ電機株式会社製「マルチライト」)を用いて100mJ/cm2のghi線を照射したのち、140℃、60秒間の条件で加熱処理を行った。
前記感光性組成物又は比較対照用感光性組成物を5インチシリコンウェハー上に約1μmの厚さになるようにスピンコーターで塗布し、110℃のホットプレート上で60秒乾燥させた。得られたウェハー上にラインアンドスペースが1:1であり、ライン幅が1〜10μmまで1μmごとに設定されたレジストマスクを密着させた。先のアルカリ現像性評価の場合と同様の方法でghi線を照射し、アルカリ現像操作を行った。ghi線露光量を30mJ/cm2から5mJ/cm2毎に増加させ、ライン幅3μmを忠実に再現することのできる露光量(Eop露光量)で評価した。
前記感光性組成物又は比較対照用感光性組成物を5インチシリコンウェハー上に約1μmの厚さになるようにスピンコーターで塗布し、110℃のホットプレート上で60秒乾燥させた。得られたウェハー上にフォトマスクを乗せ、先のアルカリ現像性評価の場合と同様の方法でghi線100mJ/cm2を照射し、アルカリ現像操作を行った。レーザーマイクロスコープ(株式会社キーエンス製「VK−8500」)を用いてパターン状態を確認し、L/S=5μmで解像できているものを○、L/S=5μmで解像できていないものを×として評価した。
前記感光性組成物又は比較対照用感光性組成物を5インチシリコンウェハー上に約1μmの厚さになるようにスピンコーターで塗布し、110℃のホットプレート上で60秒乾燥させた。得られたウェハーから樹脂分をかきとり、そのガラス転移温度(Tg)を測定した。ガラス転移温度(Tg)の測定は示差走査熱量計(DSC)(株式会社TAインスツルメント製「Q100」)を用いて、窒素雰囲気下、温度範囲−100〜200℃、昇温温度10℃/分の条件で行った。
前記感光性組成物又は比較対照用感光性組成物感光性組成物を5インチシリコンウェハー上に約1μmの厚さになるようにスピンコーターで塗布し、110℃のホットプレート上で60秒乾燥させた。得られたウェハーを85℃、湿度85%で24時間吸湿させ、吸湿前後の質量変化から吸水率を算出した。
Claims (13)
- 下記構造式(1)
で表される構造部位(I)を繰り返し単位とする変性ヒドロキシナフタレンノボラック樹脂であり、樹脂中に存在するR1のうち少なくとも一つが3級アルキル基、アルコキシアルキル基、アシル基、アルコキシカルボニル基、ヘテロ原子含有環状炭化水素基、トリアルキルシリル基の何れかであることを特徴とする変性ヒドロキシナフタレンノボラック樹脂。 - 下記構造式(2)
- 前記構造式(1)中の−O−R1で表される構造部位(R1は水素原子、3級アルキル基、アルコキシアルキル基、アシル基、アルコキシカルボニル基、ヘテロ原子含有環状炭化水素基、トリアルキルシリル基の何れかである)において、R1が3級アルキル基、アルコキシアルキル基、アシル基、アルコキシカルボニル基、ヘテロ原子含有環状炭化水素基、トリアルキルシリル基の何れかである構造部位(OX)と、R1が水素原子である構造部位(OH)との存在比率[(OX)/(OH)]が5/95〜50/50の範囲である請求項1記載の変性ヒドロキシナフタレンノボラック樹脂。
- 前記構造式(1)で表される構造部位(I)中のR1が、アルコキシアルキル基、アルコキシカルボニル基、ヘテロ原子含有環状炭化水素基の何れかである請求項1記載の変性ヒドロキシナフタレンノボラック樹脂。
- ヒドロキシナフタレン化合物とホルムアルデヒドとを疎水性の有機溶剤と水との混合溶媒中、酸触媒条件下で反応させて得られるヒドロキシナフタレンノボラック中間体を得、次いで、得られたヒドロキシナフタレンノボラック中間体のフェノール性水酸基の水素原子の一部を、3級アルキル基、アルコキシアルキル基、アシル基、アルコキシカルボニル基、環状エーテル構造部位、トリアルキルシリル基の何れかで置換した化学構造を有する請求項1記載の変性ヒドロキシナフタレンノボラック樹脂。
- ヒドロキシナフタレン化合物とホルムアルデヒドとを、疎水性の有機溶剤と水との混合溶媒中、酸触媒条件下で反応させて得られるヒドロキシナフタレンノボラック樹脂を得、次いで、得られたヒドロキシナフタレンノボラック樹脂中のフェノール性水酸基の水素原子の一部を、3級アルキル基、アルコキシアルキル基、アシル基、アルコキシカルボニル基、環状エーテル構造部位、トリアルキルシリル基の何れかで置換することを特徴とする変性ヒドロキシナフタレンノボラック樹脂の製造方法。
- 前記ヒドロキシナフタレン化合物が1−ナフトールまたは2,7―ジヒドロキシナフタレンである請求項9記載の変性ヒドロキシナフタレンノボラック樹脂の製造方法。
- 請求項1〜8の何れか一つに記載の変性ヒドロキシナフタレンノボラック樹脂と、光酸発生剤とを含有する感光性組成物。
- 請求項11に記載の感光性組成物からなるレジスト材料。
- 請求項11に記載の感光性組成物からなる塗膜。
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