JP2005122123A - 青紫レーザー感光性組成物 - Google Patents
青紫レーザー感光性組成物 Download PDFInfo
- Publication number
- JP2005122123A JP2005122123A JP2004238699A JP2004238699A JP2005122123A JP 2005122123 A JP2005122123 A JP 2005122123A JP 2004238699 A JP2004238699 A JP 2004238699A JP 2004238699 A JP2004238699 A JP 2004238699A JP 2005122123 A JP2005122123 A JP 2005122123A
- Authority
- JP
- Japan
- Prior art keywords
- group
- meth
- blue
- violet laser
- alkyl group
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 84
- 235000005811 Viola adunca Nutrition 0.000 title claims abstract description 50
- 240000009038 Viola odorata Species 0.000 title claims abstract description 50
- 235000013487 Viola odorata Nutrition 0.000 title claims abstract description 50
- 235000002254 Viola papilionacea Nutrition 0.000 title claims abstract description 50
- 150000001875 compounds Chemical class 0.000 claims abstract description 96
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 64
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 29
- 229920001577 copolymer Polymers 0.000 claims abstract description 29
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims abstract description 28
- 230000001235 sensitizing effect Effects 0.000 claims abstract description 15
- 150000003440 styrenes Chemical class 0.000 claims abstract description 12
- 239000003999 initiator Substances 0.000 claims abstract description 11
- 238000010521 absorption reaction Methods 0.000 claims abstract description 10
- 150000001735 carboxylic acids Chemical class 0.000 claims abstract description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 76
- -1 acryloyloxy groups Chemical group 0.000 claims description 71
- 125000001424 substituent group Chemical group 0.000 claims description 37
- 125000000623 heterocyclic group Chemical group 0.000 claims description 20
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 15
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 150000002148 esters Chemical class 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- FZEYVTFCMJSGMP-UHFFFAOYSA-N acridone Chemical class C1=CC=C2C(=O)C3=CC=CC=C3NC2=C1 FZEYVTFCMJSGMP-UHFFFAOYSA-N 0.000 claims description 5
- 239000000470 constituent Substances 0.000 claims description 5
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical class C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 claims description 5
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 3
- 125000000609 carbazolyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 2
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical group C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 claims description 2
- 230000035945 sensitivity Effects 0.000 abstract description 9
- 238000012545 processing Methods 0.000 abstract description 5
- 239000010408 film Substances 0.000 description 68
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- 239000000463 material Substances 0.000 description 30
- 238000000576 coating method Methods 0.000 description 26
- 239000011248 coating agent Substances 0.000 description 24
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 19
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
- 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 18
- 238000011161 development Methods 0.000 description 17
- 239000000975 dye Substances 0.000 description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 15
- 239000000758 substrate Substances 0.000 description 15
- 229910052799 carbon Inorganic materials 0.000 description 14
- 238000000034 method Methods 0.000 description 14
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 125000003277 amino group Chemical group 0.000 description 11
- 238000001035 drying Methods 0.000 description 11
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 10
- PESYEWKSBIWTAK-UHFFFAOYSA-N cyclopenta-1,3-diene;titanium(2+) Chemical class [Ti+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 PESYEWKSBIWTAK-UHFFFAOYSA-N 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- 239000011241 protective layer Substances 0.000 description 8
- 125000002252 acyl group Chemical group 0.000 description 7
- 235000011187 glycerol Nutrition 0.000 description 7
- 125000001841 imino group Chemical group [H]N=* 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 7
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 6
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 125000003342 alkenyl group Chemical group 0.000 description 6
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 6
- 150000001721 carbon Chemical group 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 125000005843 halogen group Chemical group 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 6
- 238000007747 plating Methods 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 6
- 239000004065 semiconductor Substances 0.000 description 6
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 5
- OAZWDJGLIYNYMU-UHFFFAOYSA-N Leucocrystal Violet Chemical compound C1=CC(N(C)C)=CC=C1C(C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 OAZWDJGLIYNYMU-UHFFFAOYSA-N 0.000 description 5
- 125000004442 acylamino group Chemical group 0.000 description 5
- 125000004423 acyloxy group Chemical group 0.000 description 5
- 125000003302 alkenyloxy group Chemical group 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 125000004414 alkyl thio group Chemical group 0.000 description 5
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 125000003710 aryl alkyl group Chemical group 0.000 description 5
- 125000004104 aryloxy group Chemical group 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 5
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 5
- 125000000392 cycloalkenyl group Chemical group 0.000 description 5
- 125000000753 cycloalkyl group Chemical group 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- 239000005056 polyisocyanate Substances 0.000 description 5
- 229920001228 polyisocyanate Polymers 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 239000000600 sorbitol Substances 0.000 description 5
- 125000002130 sulfonic acid ester group Chemical group 0.000 description 5
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 4
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- 244000172533 Viola sororia Species 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 125000005018 aryl alkenyl group Chemical group 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 125000004093 cyano group Chemical group *C#N 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 238000005530 etching Methods 0.000 description 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 4
- DZFWNZJKBJOGFQ-UHFFFAOYSA-N julolidine Chemical group C1CCC2=CC=CC3=C2N1CCC3 DZFWNZJKBJOGFQ-UHFFFAOYSA-N 0.000 description 4
- 238000010030 laminating Methods 0.000 description 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 125000000542 sulfonic acid group Chemical group 0.000 description 4
- 125000000147 tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 4
- BPXVHIRIPLPOPT-UHFFFAOYSA-N 1,3,5-tris(2-hydroxyethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound OCCN1C(=O)N(CCO)C(=O)N(CCO)C1=O BPXVHIRIPLPOPT-UHFFFAOYSA-N 0.000 description 3
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 3
- GBOJZXLCJZDBKO-UHFFFAOYSA-N 2-(2-chlorophenyl)-2-[2-(2-chlorophenyl)-4,5-diphenylimidazol-2-yl]-4,5-diphenylimidazole Chemical compound ClC1=CC=CC=C1C1(C2(N=C(C(=N2)C=2C=CC=CC=2)C=2C=CC=CC=2)C=2C(=CC=CC=2)Cl)N=C(C=2C=CC=CC=2)C(C=2C=CC=CC=2)=N1 GBOJZXLCJZDBKO-UHFFFAOYSA-N 0.000 description 3
- 125000006276 2-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C(*)C([H])=C1[H] 0.000 description 3
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
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- 238000005286 illumination Methods 0.000 description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
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- YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 description 2
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- YKXVZTWMMZZVRA-UHFFFAOYSA-N CC1(C=CC=C1)[Ti]C1(C=CC=C1)C Chemical compound CC1(C=CC=C1)[Ti]C1(C=CC=C1)C YKXVZTWMMZZVRA-UHFFFAOYSA-N 0.000 description 2
- JUQPZRLQQYSMEQ-UHFFFAOYSA-N CI Basic red 9 Chemical compound [Cl-].C1=CC(N)=CC=C1C(C=1C=CC(N)=CC=1)=C1C=CC(=[NH2+])C=C1 JUQPZRLQQYSMEQ-UHFFFAOYSA-N 0.000 description 2
- 0 CN(CCc(c(*)c1)c(*)cc1C(*)=NS(*)(=O)=O)*I Chemical compound CN(CCc(c(*)c1)c(*)cc1C(*)=NS(*)(=O)=O)*I 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004641 Diallyl-phthalate Substances 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
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- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
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- Exposure And Positioning Against Photoresist Photosensitive Materials (AREA)
- Materials For Photolithography (AREA)
- Polymerisation Methods In General (AREA)
Abstract
【解決手段】 下記の(A)成分、(B)成分、(C)成分、及び(D)成分を含有する青紫レーザー感光性組成物。
(A)エチレン性不飽和カルボン酸類、アルキル(メタ)アクリレート類、及びスチレン類に由来する各構成繰返し単位を含むカルボキシル基含有共重合体
(B)エチレン性不飽和化合物
(C)光重合開始剤
(D)355〜430nmの波長域に吸収極大を有する増感色素
Description
、側鎖にエチレン性不飽和結合を有せしめた特定の高分子結合材等を組み合わせた光重合性組成物を感光性層とする平版印刷版(例えば、特許文献1参照。)も提案されている。しかしながら、そこに開示される感光性組成物層は、平版印刷版用であるが故、膜厚が薄く、膜厚が5μm以上と厚いレジスト画像形成用として用いた場合においては、青紫レーザー光による露光感度が充分ではなく、現像性にも劣ると共に、高分子結合材中に残存するエポキシ基含有エチレン性不飽和化合物の影響か、レジスト加工後のレジスト画像の剥離、除去が困難であるという問題があった。
(A)エチレン性不飽和カルボン酸類、アルキル(メタ)アクリレート類、及びスチレン類に由来する各構成繰返し単位を含むカルボキシル基含有共重合体
(B)エチレン性不飽和化合物
(C)光重合開始剤
(D)355〜430nmの波長域に吸収極大を有する増感色素
ル(メタ)アクリレート、エチル(メタ)アクリレート、n−又はi−プロピル(メタ)アクリレート、n−又はi−又はt−ブチル(メタ)アクリレート、n−ペンチル(メタ)アクリレート、n−ヘキシル(メタ)アクリレート、n−ドデシル(メタ)アクリレート、2−エチルヘキシル(メタ)アクリレート等が挙げられ、中で、メチル(メタ)アクリレート、エチル(メタ)アクリレート、n−又はi−又はt−ブチル(メタ)アクリレート、2−エチルヘキシル(メタ)アクリレート等が特に好ましい。
特に好ましく、又、30重量%以下であるのが好ましく、20重量%以下であるのが特に好ましい。
合物とポリイソシアネート化合物とのウレタン(メタ)アクリレート類、及び、(メタ)アクリル酸又はヒドロキシ(メタ)アクリレート化合物とポリエポキシ化合物とのエポキシ(メタ)アクリレート類等が挙げられる。
に到らしめるラジカル発生剤であって、例えば、ヘキサアリールビイミダゾール系化合物、チタノセン系化合物、ハロメチル化s−トリアジン誘導体、ハロメチル化1,3,4−オキサジアゾール誘導体、ジアリールヨードニウム塩、有機硼素酸塩、及び有機過酸化物等が挙げられる。中で、感光性組成物としての感度、基板に対する密着性、及び保存安定性等の面から、ヘキサアリールビイミダゾール系化合物、及びチタノセン系化合物が好ましく、ヘキサアリールビイミダゾール系化合物が特に好ましい。
アルキルイミノ基を示し、複素環に縮合するベンゼン環は置換基を有していてもよい。〕
−1,3,4−オキサジアゾール、2,5−ビス(p−ジエチルアミノフェニル)−1,3,4−チアジアゾール等が挙げられる。
グリーン、エオシン、エチルバイオレット、エリスロシンB、メチルグリーン、クリスタルバイオレット、ベイシックフクシン、フェノールフタレイン、1,3−ジフェニルトリアジン、アリザリンレッドS、チモールフタレイン、メチルバイオレット2B、キナルジンレッド、ローズベンガル、メタニルイエロー、チモールスルホフタレイン、キシレノールブルー、メチルオレンジ、オレンジIV、ジフェニルチオカルバゾン、2,7−ジクロロフルオレセイン、パラメチルレッド、コンゴーレッド、ベンゾプルプリン4B、α−ナフチルレッド、ナイルブルーA、フェナセタリン、メチルバイオレット、マラカイトグリーン、パラフクシン、オイルブルー♯603〔オリエント化学工業社製〕、ビクトリアピュアブルーBOH、スピロンブルーGN〔保土ヶ谷化学工業社製〕、ローダミン6G等挙げられ、中で、ロイコクリスタルバイオレット等のロイコ染料を感光性組成物の全量に対して0.01〜1.5重量%、特には0.05〜0.8重量%含有し、更に、クリスタルバイオレット、マカライトグリーン、ブリリアントグリーン等を0.001〜0.5重量%、特には0.002〜0.2重量%含有するのが好ましい。
ノエチルエーテルアセテート、プロピレングリコールモノブチルエーテルアセテート、ジプロピレングリコールジメチルエーテル等のプロピレングリコール系溶剤、酢酸ブチル、酢酸アミル、酪酸エチル、酪酸ブチル、ジエチルオキサレート、ピルビン酸エチル、エチル−2−ヒドロキシブチレート、エチルアセトアセテート、乳酸メチル、乳酸エチル、3−メトキシプロピオン酸メチル等のエステル系溶剤、メタノール、イソプロパノール、ヘプタノール、ヘキサノール、ジアセトンアルコール、フルフリルアルコール等のアルコール系溶剤、シクロヘキサノン、メチルエチルケトン等のケトン系溶剤、トルエン等の芳香族系溶剤、ジメチルホルムアミド、ジメチルアセトアミド、N−メチルピロリドン等の高極性溶剤、或いはこれらの混合溶剤、更にはこれらに芳香族炭化水素を添加したもの等が挙げられる。これらの中で、溶解能、表面張力、粘度、乾燥のし易さ等の点から、メチルエチルケトン、メタノール、イソプロパノール、トルエン等の単独或いは混合溶剤が好適である。溶剤の使用割合は、感光性組成物の総量に対して、通常、重量比で0.5〜2倍程度の範囲である。
い。
成した金属張積層板が、好ましく用いられる。
青紫レーザー感光性組成物として、下記のカルボキシル基含有共重合体(A1〜A7)、エチレン性不飽和化合物(B1〜B4)、光重合開始剤(C1〜C2)、増感色素(D1〜D2)、及びその他成分(X1〜X2)を、表2に示す処方で下記の溶剤(Y1)に加えて、室温で攪拌して調液した塗布液を、仮支持フィルムとしてのポリエチレンテレフ
タレートフィルム(厚み25μm)上に、100μmのアプリケーターを用いて乾燥膜厚が20μmとなる量で塗布し、90℃のオーブンで10分間乾燥させ、形成された青紫レーザー感光性組成物層上に、被覆フィルムとしてのポリエチレンフィルム(厚み25μm)を積層し、ドライフィルムレジスト材を作製した。
次表1に示す(A1)〜(A7)の共重合体
(B1)下記の化合物
(B2)下記の化合物
(B3)下記の化合物
(B4)下記の化合物
(C1)2,2’−ビス(o−クロロフェニル)−4,4’,5,5’−テトラフェニルビイミダゾール
(C2)ジシクロペンタジエニルチタニウムビス〔2,6−ジフルオロ−3−(1−ピロリル)フェニル〕
(D1)下記の化合物(増感色素をテトラヒドロフランで60,000倍に希釈し、300〜500nmの波長域でUV吸光係数を測定したときの、最も長波長に存在する吸収極大365nm)
(D2)下記の化合物(同上吸収極大352nm)
(X1)ロイコクリスタルバイオレット
(X2)クリスタルバイオレット
<溶剤>
(Y1)メチルエチルケトン
発振波長407nm、定格光出力500mWの日亜化学工業社製、青色LDスロットモジュール「NDAV520E2」を用い、ビームスポット径8μm、像面光量0.4mW/cm2 で、4.0mJ/cm2 、5.6mJ/cm2 8.0mJ/cm2 、11.2mJ/cm2 、16.0mJ/cm2 、及び22.3mJ/cm2 の6段階の露光量として、20μmの集合線(ライン/スペース=20μm/20μm)、20μmの独立ライン、20μmの独立スペースの露光パターンを走査露光した。露光後、20分経過してから、ポリエチレンテレフタレートフィルムを剥離、除去し、次いで、25℃で0.7重量%炭酸ナトリウム水溶液をブレークポイント(非露光部が完全に溶解するまでの時間)の1.5倍の現像時間で、0.15MPaでスプレーすることにより現像した。
各露光量で得られたパターン画像を光学顕微鏡で、集合線、独立ライン、独立スペースの解像状態を観察し、以下の基準で露光感度を評価した。
○;集合線、独立ライン、独立スペースの全てが解像。
△;集合線、独立ライン、独立スペースのうちの2種が解像。
×;集合線、独立ライン、独立スペースのうち、解像は1種以下。
前記の露光条件で、解像状態の評価が「○」となる最小露光量で走査露光した。露光後、20分経過してから、ポリエチレンテレフタレートフィルムを剥離、除去し、次いで、25℃で0.7重量%炭酸ナトリウム水溶液をブレークポイント(非露光部が完全に溶解するまでの時間)の1.2倍、1.5倍、及び2.0倍の現像時間で、0.15MPaでスプレーすることにより現像した。
各現像時間で得られたパターン画像を光学顕微鏡で、パターンのスペース部の抜け状態とライン部の幅再現状態、及び密着状態を観察し、以下の基準で評価した。
○;スペース部は完全に抜けており、ライン部も幅17〜23μmで再現。
×;スペース部が抜けきっていないか、ライン部が浮いていたり、膨潤してうねっていたり、幅が16μm以下に細っていたり、24μm以上に太っていたり、欠落している。
<レジスト画像の剥離・除去性>
45℃の3重量%水酸化ナトリウム水溶液に1分間浸漬した後のレジスト画像の剥離状況を観察し、以下の基準で評価した。
○;レジスト画像を完全に剥離・除去可。
×;レジスト画像の剥離・除去が不完全、又は、残像が残る。
<黄色灯下セーフセイト性>
レジスト画像形成材を、青紫レーザー感光性組成物層面の半分を遮光して、黄色灯照明下に、光源から1m離して(照度150ルックス)1時間放置した後、前記の露光・現像条件下で、露光、現像処理し、以下の基準で評価し、結果を表2に示した。
○;黄色灯照射部の現像時間が遮光部の現像時間の1.05倍未満。
△;黄色灯照射部の現像時間が遮光部の現像時間の1.05倍以上1.1倍未満。
×;黄色灯暴露部の現像時間が遮光部の現像時間の1.1倍以上。
用いられる。
Claims (9)
- 下記の(A)成分、(B)成分、(C)成分、及び(D)成分を含有してなることを特徴とする青紫レーザー感光性組成物。
(A)エチレン性不飽和カルボン酸類、アルキル(メタ)アクリレート類、及びスチレン類に由来する各構成繰返し単位を含むカルボキシル基含有共重合体
(B)エチレン性不飽和化合物
(C)光重合開始剤
(D)355〜430nmの波長域に吸収極大を有する増感色素 - (A)成分のカルボキシル基含有共重合体のエチレン性不飽和カルボン酸類、アルキル(メタ)アクリレート類、及びスチレン類に由来する各構成繰返し単位の含有量が、共重合体の全構成繰返し単位に対して、各々、10〜50重量%、15〜80重量%、及び1〜40重量%である請求項1に記載の青紫レーザー感光性組成物。
- (A)成分のカルボキシル基含有共重合体が、更に、ヒドロキシアルキル(メタ)アクリレート類に由来する構成繰返し単位を含み、その含有量が、共重合体の全構成繰返し単位に対して、1〜30重量%である請求項2に記載の青紫レーザー感光性組成物。
- (A)成分のカルボキシル基含有共重合体のアルキル(メタ)アクリレート類に由来する構成繰返し単位として、炭素数4以上のアルキル基によるアルキル(メタ)アクリレート類に由来する構成繰返し単位を含み、その含有量が、アルキル(メタ)アクリレート類に由来する構成繰返し単位の全量に対して、15〜60重量%である請求項2又は3に記載の青紫レーザー感光性組成物。
- (A)成分のカルボキシル基含有共重合体の炭素数4以上のアルキル基によるアルキル(メタ)アクリレート類に由来する構成繰返し単位において、炭素数4以上のアルキル基が直鎖状アルキル基と分岐状アルキル基とを含み、両者の割合が、直鎖状アルキル基:分岐状アルキル基=0.3〜0.7:0.7〜0.3である請求項4に記載の青紫レーザー感光性組成物。
- (B)成分のエチレン性不飽和化合物として、ポリオキシアルキレン基を有し、(メタ)アクリロイルオキシ基を2個以上有するエステル(メタ)アクリレート類を含む請求項1乃至5のいずれかに記載の青紫レーザー感光性組成物。
- (C)成分の光重合開始剤として、ヘキサアリールビイミダゾール系化合物を含む請求項1乃至6のいずれかに記載の青紫レーザー感光性組成物。
- (D)成分の増感色素として、ジアルキルアミノベンゼン系化合物、トリフェニルアミン系化合物、アクリドン系化合物、及びカルバゾール系化合物からなる群から選択されたいずれかの化合物を含む請求項1乃至7のいずれかに記載の青紫レーザー感光性組成物。
- ジアルキルアミノベンゼン系化合物が、下記一般式(I) で表されるジアルキルアミノベンゾフェノン系化合物、下記一般式(III) で表されるスルホニルイミノ基を有するジアルキルアミノベンゼン系化合物、及び下記一般式(IV)で表されるカルボスチリル骨格を形成したジアルキルアミノベンゼン系化合物からなる群より選択されたいずれかの化合物である請求項8に記載の青紫レーザー感光性組成物。
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