JP2001005178A - Image forming method, multilayer circuit board, and multilayer film used for the same - Google Patents
Image forming method, multilayer circuit board, and multilayer film used for the sameInfo
- Publication number
- JP2001005178A JP2001005178A JP11172421A JP17242199A JP2001005178A JP 2001005178 A JP2001005178 A JP 2001005178A JP 11172421 A JP11172421 A JP 11172421A JP 17242199 A JP17242199 A JP 17242199A JP 2001005178 A JP2001005178 A JP 2001005178A
- Authority
- JP
- Japan
- Prior art keywords
- insulating layer
- resin insulating
- optical density
- average optical
- layer
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 34
- 229920005989 resin Polymers 0.000 claims abstract description 115
- 239000011347 resin Substances 0.000 claims abstract description 115
- 230000003287 optical effect Effects 0.000 claims abstract description 52
- 239000000758 substrate Substances 0.000 claims abstract description 42
- 238000007747 plating Methods 0.000 claims abstract description 25
- 230000001678 irradiating effect Effects 0.000 claims description 2
- 230000002950 deficient Effects 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 96
- 239000000243 solution Substances 0.000 description 23
- 239000010419 fine particle Substances 0.000 description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 13
- 239000010949 copper Substances 0.000 description 11
- 229910052802 copper Inorganic materials 0.000 description 11
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000002585 base Substances 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 238000005553 drilling Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 238000000206 photolithography Methods 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- -1 polypropylene Polymers 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000975 dye Substances 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 238000009413 insulation Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 238000007788 roughening Methods 0.000 description 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- VBUISAAVVYXFHI-BTJKTKAUSA-N (z)-but-2-enedioic acid;phenylmethanamine Chemical compound NCC1=CC=CC=C1.OC(=O)\C=C/C(O)=O VBUISAAVVYXFHI-BTJKTKAUSA-N 0.000 description 2
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical compound ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000011889 copper foil Substances 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 229910000679 solder Inorganic materials 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 description 1
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 101001062854 Rattus norvegicus Fatty acid-binding protein 5 Proteins 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- XKRFYHLGVUSROY-UHFFFAOYSA-N argon Substances [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical group [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 229960000956 coumarin Drugs 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000013527 degreasing agent Substances 0.000 description 1
- 238000005237 degreasing agent Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000007772 electroless plating Methods 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000003574 free electron Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- CPBQJMYROZQQJC-UHFFFAOYSA-N helium neon Chemical compound [He].[Ne] CPBQJMYROZQQJC-UHFFFAOYSA-N 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000006224 matting agent 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
- 239000007769 metal material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052863 mullite Inorganic materials 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229920003192 poly(bis maleimide) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920006316 polyvinylpyrrolidine Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Photosensitive Polymer And Photoresist Processing (AREA)
- Materials For Photolithography (AREA)
- Production Of Multi-Layered Print Wiring Board (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は樹脂絶縁層への画像
形成方法、多層配線基板及びこれに用いられる多層フィ
ルムに関し、さらに詳しくはビルドアップ法による多層
配線基板(ビルドアップ基板)の製造方法、該製造方法
を用いて製造された多層配線基板、及び該製造方法に用
いられる多層フィルムに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for forming an image on a resin insulating layer, a multilayer wiring board and a multilayer film used for the same, and more particularly to a method for manufacturing a multilayer wiring board (build-up board) by a build-up method. The present invention relates to a multilayer wiring board manufactured by using the manufacturing method, and a multilayer film used in the manufacturing method.
【0002】[0002]
【従来の技術】近年、電子機器の軽薄短小化、高機能
化、薄層化の流れが急速に進んできている。このため、
電子部品を高密度に実装することが必須となり、これに
対応するため、プリント配線基板の高密度化が大きな課
題となってきている。プリント配線基板の高密度化の方
法としてビルドアップ法が注目を集めている。その特徴
は、従来ドリルを用いて基板を貫通するスルーホールを
形成することによって基板両面の配線層間の接続を行っ
ていたところを、光を用いて基板表層の樹脂絶縁層にビ
アホールと呼ばれる穴をあけ、層間接続部を形成するこ
とにある。光を用いた穴あけ加工は、ドリルによる穴あ
け加工(直径1mm程の穴)より著しく小さなサイズ
(直径200μm以下)の穴あけが可能であり、これに
より基板の高密度化が可能となった。この光を用いた穴
あけ方法にはレーザーを用いた穴あけ方法とフォトリソ
グラフィーを用いた穴あけ方法とがある。2. Description of the Related Art In recent years, electronic equipment has been rapidly becoming lighter, smaller, more functional, and thinner. For this reason,
It is essential to mount electronic components at high density, and in order to cope with this, increasing the density of printed wiring boards has become a major issue. The build-up method has attracted attention as a method for increasing the density of printed wiring boards. The feature is that the connection between the wiring layers on both sides of the board was made by forming a through hole penetrating the board using a conventional drill, but a hole called a via hole was formed in the resin insulation layer on the surface of the board using light. Opening is to form an interlayer connection. Drilling using light enables drilling of a significantly smaller size (200 μm or less in diameter) than drilling (a hole having a diameter of about 1 mm), thereby enabling high-density substrates. Drilling methods using this light include a drilling method using a laser and a drilling method using photolithography.
【0003】レーザーを用いた穴あけ方法は、レーザー
の直進性が良く広がりが少ないため、加工精度が良く、
通常、直径100μmレベルの加工が可能である。しか
し、この方法は、フォトエッチングした小開口毎にレー
ザーを移動しながら1つずつ順番に加工しなければなら
ないため、生産性が悪い。[0003] A laser drilling method has good processing accuracy because the laser has good straightness and little spread.
Usually, processing at a level of 100 μm in diameter is possible. However, this method is inferior in productivity because the laser must be moved one by one while moving the laser for each of the small openings etched.
【0004】一方、フォトリソグラフィを用いた穴あけ
方法は、一度の露光、現像により多数のビアホールを形
成できるため、生産性は良いが、露光に用いる光(通
常、紫外線)の広がりは回折現象などにより大きい。こ
のため、通常、フォトリソグラフィ法では直径150μ
m以下のビアホールを形成するのは困難である。[0004] On the other hand, a hole making method using photolithography can form a large number of via holes by one-time exposure and development, so that productivity is good. However, the spread of light (usually, ultraviolet light) used for exposure is affected by a diffraction phenomenon or the like. large. For this reason, a diameter of 150 μm is usually used in the photolithography method.
It is difficult to form a via hole of m or less.
【0005】[0005]
【発明が解決しようとする課題】基板の高密度化の要求
は年々高まり、直径が100μm以下(60μm以下、
40μm以下)のビアホールが要求されるようになって
きた。このような小さな直径のビアホールを有する多層
配線基板ではビアホールの接続不良が発生する確率が高
くなった。The demand for high-density substrates is increasing year by year, and the diameter of the substrate is 100 μm or less (60 μm or less,
Via holes of 40 μm or less have been required. In a multilayer wiring board having such a small-diameter via hole, there is a high probability that a connection failure of the via hole occurs.
【0006】本発明の課題は、小さな直径のビアホール
の接続不良を改善することにある。An object of the present invention is to improve poor connection of a via hole having a small diameter.
【0007】[0007]
【課題を解決するための手段】本発明者は前記課題が、
樹脂絶縁層の一方の面から半分の厚みまでの平均光学濃
度分率が、該樹脂絶縁層のもう一方の面から半分の厚み
までの平均光学濃度分率の1.2倍から500倍に形成
することによって解決されることを見出し、本発明を完
成するに至った。Means for Solving the Problems The present inventor has solved the above problem,
The average optical density fraction from one surface to half the thickness of the resin insulating layer is 1.2 to 500 times the average optical density fraction from the other surface to half the thickness of the resin insulating layer. Thus, the present invention has been completed.
【0008】即ち、本発明は一方の面から半分の厚みま
での平均光学濃度分率が、他方の面から半分の厚みまで
の平均光学濃度分率の1.2倍から500倍であり、平
均光学濃度分率の低い方の面がその上にメッキ層を保持
することが可能である樹脂絶縁層の平均光学濃度分率が
低い方の面から光を照射して画像を形成することを特徴
とする画像形成方法を提供する。That is, according to the present invention, the average optical density fraction from one surface to half the thickness is 1.2 to 500 times the average optical density fraction from the other surface to half the thickness. An image is formed by irradiating light from the surface with the lower average optical density fraction of the resin insulating layer on which the surface with the lower optical density fraction can hold the plating layer thereon. And an image forming method.
【0009】また、本発明はベース基板の少なくとも片
面に、少なくとも2層の配線と少なくとも1層の樹脂絶
縁層が形成されるように配線と樹脂絶縁層とが交互に配
置され、上下の配線を電気的に接続するビアホールが樹
脂絶縁層に形成された多層配線基板であって、各樹脂絶
縁層の基板側の面から層の半分の厚みまでの平均光学濃
度分率が該絶縁層の基板と反対側の面から層の半分の厚
みまでの平均光学濃度分率の1.2倍から500倍であ
る多層配線基板を提供する。Further, according to the present invention, the wiring and the resin insulating layer are alternately arranged on at least one surface of the base substrate so that at least two wirings and at least one resin insulating layer are formed. A multilayer wiring board in which via holes to be electrically connected are formed in a resin insulating layer, and the average optical density fraction from the substrate side surface of each resin insulating layer to half the thickness of the layer is the same as that of the insulating layer substrate. Provided is a multilayer wiring board having an average optical density fraction of 1.2 to 500 times the thickness from the opposite side to half the thickness of the layer.
【0010】さらに、本発明は光照射によりビアホール
を形成可能な第一の樹脂絶縁層と第二の樹脂絶縁層から
なり、第一の樹脂絶縁層がその上にメッキ層を保持する
ことが可能であり、第二の樹脂絶縁層の平均光学濃度分
率が第一の樹脂絶縁層の平均光学濃度分率の1.2倍か
ら500倍である多層フィルムを提供する。Further, the present invention comprises a first resin insulating layer and a second resin insulating layer capable of forming a via hole by light irradiation, and the first resin insulating layer can hold a plating layer thereon. Wherein the average optical density fraction of the second resin insulation layer is 1.2 to 500 times the average optical density fraction of the first resin insulation layer.
【0011】本発明では、樹脂絶縁層の光照射側の半分
の平均光学濃度分率がもう半分のそれの1.2から50
0倍であるため、微細なビアホールを形成するために照
射された光が樹脂絶縁層の下まで到達すると共に、樹脂
絶縁層の下部で完全に吸収されるため、配線によって反
射されることがない。According to the present invention, the average optical density fraction of half of the resin insulating layer on the light irradiation side is 1.2 to 50 of that of the other half.
Since it is 0 times, the light irradiated to form a fine via hole reaches below the resin insulating layer and is completely absorbed below the resin insulating layer, so that it is not reflected by the wiring. .
【0012】[0012]
【発明の実施の形態】以下、本発明を詳細に説明する。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail.
【0013】本発明のベース基板には、絶縁材料、金属
材料等種々の材質を用いることができる。絶縁材料に
は、有機材料、無機材料又は両者の複合体を用いること
ができるが、ガラス布にエポキシ樹脂を含浸させたも
の、例えば、NEMA規格FR−4やセラミックスが好
ましく用いられる。ベース基板には、NEMA規格FR
−5やBT(ビスマレイミドトリアジン系樹脂)などの
樹脂を用いることもできる。Various materials such as an insulating material and a metal material can be used for the base substrate of the present invention. As the insulating material, an organic material, an inorganic material, or a composite of both can be used. However, a material obtained by impregnating a glass cloth with an epoxy resin, for example, NEMA standard FR-4 or ceramics is preferably used. NEMA standard FR for base substrate
Resins such as -5 and BT (bismaleimide triazine-based resin) can also be used.
【0014】本発明ではベース基板の少なくとも片面に
はまず配線が設けられ、その後樹脂絶縁層と配線が交互
に形成される。本発明では、少なくとも2層の配線と少
なくとも1層の樹脂絶縁層を備える。In the present invention, a wiring is first provided on at least one surface of the base substrate, and thereafter, a resin insulating layer and a wiring are alternately formed. In the present invention, at least two wiring layers and at least one resin insulating layer are provided.
【0015】配線に用いられる材料としては、銀、銅、
アルミニウム等の金属が挙げられる。As materials used for wiring, silver, copper,
Metals such as aluminum are exemplified.
【0016】樹脂絶縁層は、上記樹脂バインダーの他、
光照射に用いられる波長の光を吸収する成分、例えば、
色素、光重合開始剤、モノマー等を含有することができ
る。好ましくは、特開平7−110577号公報、特開
平7−209866号公報等に開示されるような、光重
合開始剤あるいは光重合開始剤系とエチレン性不飽和二
重結合を有する付加重合性モノマー、及びスチレン/マ
レイン酸無水物共重合体のアミン(ベンジルアミン、シ
クロへキシルアミン等)変性した樹脂を含有する光重合
性組成物等が用いられる。[0016] In addition to the above resin binder, the resin insulating layer
A component that absorbs light having a wavelength used for light irradiation, for example,
It can contain a dye, a photopolymerization initiator, a monomer, and the like. Preferably, an addition-polymerizable monomer having a photopolymerization initiator or a photopolymerization initiator system and an ethylenically unsaturated double bond, as disclosed in JP-A-7-110577 and JP-A-7-209866. And a photopolymerizable composition containing a resin modified with an amine (benzylamine, cyclohexylamine, etc.) of a styrene / maleic anhydride copolymer.
【0017】本発明に用いられる色素には染料(溶媒に
可溶な光吸収性物質)と顔料(溶媒に不溶な光吸収性物
質)がある。The dyes used in the present invention include dyes (light-absorbing substances soluble in solvents) and pigments (light-absorbing substances insoluble in solvents).
【0018】照射する光が紫外光の場合、染料としては
サリシレート系、ベンゾフェノン系、ベンゾトリアゾー
ル系、クマリン系等の紫外線吸収剤が用いられる。ま
た、照射する光が紫外光の場合、顔料としてはアセチレ
ンブラックのようなカーボンブラック、C.I.=PB
15:6のように紫外部まで吸収する顔料などがある。When the light to be irradiated is ultraviolet light, a salicylate-based, benzophenone-based, benzotriazole-based or coumarin-based ultraviolet absorber is used as a dye. When the light to be irradiated is ultraviolet light, carbon black such as acetylene black, C.I. I. = PB
For example, there is a pigment such as 15: 6 that absorbs ultraviolet rays.
【0019】樹脂絶縁層の厚みは1〜50μmが好まし
く、2〜40μmがより好ましく、5〜30μmが特に
好ましい。The thickness of the resin insulating layer is preferably 1 to 50 μm, more preferably 2 to 40 μm, and particularly preferably 5 to 30 μm.
【0020】本発明では樹脂絶縁層の光照射側と反対側
(基板側)の面から半分の厚みまでの平均光学濃度分率
が該樹脂層の光照射側(基板と反対側)の面から半分の
厚みまでの平均光学濃度分率の1.2倍から500倍に
形成される。In the present invention, the average optical density fraction from the surface on the side opposite to the light irradiation side (substrate side) of the resin insulating layer to half the thickness is from the surface on the light irradiation side (opposite side to the substrate) of the resin layer. It is formed at a ratio of 1.2 to 500 times the average optical density fraction up to half the thickness.
【0021】本発明において、光学濃度(OD)とは、
光照射に用いられる波長の光が樹脂絶縁層を通過する際
に吸収される程度をいう。In the present invention, the optical density (OD) is
It refers to the degree to which light having the wavelength used for light irradiation is absorbed when passing through the resin insulating layer.
【0022】該波長の光が入射する時の強度をI0、通
過後の強度をIとすると、OD=log10(I0/I)
で計算される。Assuming that the intensity when the light of the wavelength enters is I 0 and the intensity after passing is I, OD = log 10 (I 0 / I)
Is calculated.
【0023】樹脂絶縁層に該波長の光を散乱、反射、屈
折させる性質がある場合、予めその量を見積もっておく
などして実測値を補正し、吸収のみの値を計算する。If the resin insulating layer has the property of scattering, reflecting, and refracting light of the wavelength, the measured value is corrected by estimating the amount in advance, and the value of only absorption is calculated.
【0024】本発明では「光学濃度分率」を微小厚みあ
たりのODを厚み1μmあたりのODに換算した値」と
定義する。その求め方は一例として樹脂層の微小厚み部
分の厚みd(μm)とODを測定し「光学濃度分率=O
D/d」なる式で算出する。In the present invention, the “optical density fraction” is defined as a value obtained by converting an OD per minute thickness into an OD per 1 μm thickness. For example, the thickness is determined by measuring the thickness d (μm) and the OD of the minute thickness portion of the resin layer, and “optical density fraction = O
D / d ”.
【0025】本発明では「平均光学濃度分率」とは「対
象となる厚み方向領域の光学濃度分率の平均」と定義す
る。その求め方は一例として、対象となる厚み方向領域
の光学濃度分率と、その領域の厚みd2(μm)を測定
し「平均光学濃度分率=OD/d2」なる式で算出す
る。In the present invention, the “average optical density fraction” is defined as “the average of the optical density fractions in the target region in the thickness direction”. As an example, the optical density fraction of the target thickness direction region and the thickness d 2 (μm) of the target region are measured and calculated by the formula “average optical density fraction = OD / d 2 ”.
【0026】平均光学濃度分率が1.2未満であると、
樹脂絶縁層の下に到達した光が樹脂絶縁層と配線との界
面で反射され、ビアホールの信頼性が低下する。また、
平均光学濃度分率が500倍を超えると、照射された光
が樹脂絶縁層の下に到達しないため、ビアホールの信頼
性が低下する。平均光学濃度分率は2から200が好ま
しく、4から100がもっとも好ましい。When the average optical density fraction is less than 1.2,
Light that has reached below the resin insulating layer is reflected at the interface between the resin insulating layer and the wiring, and the reliability of the via hole is reduced. Also,
If the average optical density fraction exceeds 500 times, the irradiated light does not reach below the resin insulating layer, so that the reliability of the via hole decreases. The average optical density fraction is preferably from 2 to 200, most preferably from 4 to 100.
【0027】樹脂絶縁層は、配線上に異なる組成の樹脂
溶液を塗布したり、フィルムを配線上に貼り付けたり、
塗布とフィルム貼り付けを併用することで形成すること
ができる。The resin insulating layer is formed by applying a resin solution having a different composition onto the wiring, attaching a film on the wiring,
It can be formed by using both application and film attachment.
【0028】塗布する場合には、1層目の樹脂絶縁層を
塗布し、乾燥した後に、2層目を塗布し、乾燥する逐次
塗布、1層目が乾燥する前に2層目を塗布する同時重層
塗布、1回の塗布で塗布操作を終了し、塗布後、乾燥中
に光吸収成分を沈降させる方法、1回の塗布で塗布操作
を終了し、塗布後に乾燥中の溶媒の移動によって光吸収
成分を移動させる方法等のいずれも使用できる。In the case of application, the first resin insulating layer is applied, dried, then the second layer is applied, and dried sequentially. The first layer is applied before the second layer is dried. Simultaneous multi-layer coating, a method in which the coating operation is completed with one coating, and the light absorbing component is allowed to settle during drying after the coating. Any of the methods for moving the absorption component can be used.
【0029】また、基板側の層に使用される樹脂溶液又
はフィルムの色素、光重合開始剤、バインダー、モノマ
ー等の光吸収成分の濃度は基板と反対側の層に使用され
る樹脂溶液又はフィルムのそれより濃くする。The concentration of a light absorbing component such as a dye, a photopolymerization initiator, a binder, and a monomer in the resin solution or film used in the layer on the substrate side is determined by the resin solution or film used in the layer on the side opposite to the substrate. Thicker than that of
【0030】塗布に使用する溶剤としては、メチルエチ
ルケトン、シクロヘキサノン等が好適に用いられる。As a solvent used for coating, methyl ethyl ketone, cyclohexanone and the like are preferably used.
【0031】樹脂溶液の塗布後に表面を保護するためポ
リプロピレンフィルム、ポリエチレンフィルム等を樹脂
絶縁層にラミネートしてもよい。After the application of the resin solution, a polypropylene film, a polyethylene film or the like may be laminated on the resin insulating layer to protect the surface.
【0032】塗布と、貼り合わせでは予め多層構成にし
たフィルムを配線上に貼り付けることがより好ましい。In application and lamination, it is more preferable to laminate a film having a multilayer structure in advance on the wiring.
【0033】樹脂絶縁層に多層フィルムを用いる場合に
は、多層フィルムは配線形成済みのベース基材上にラミ
ネートされるので、経時でラミネート性を阻害する程度
に樹脂の硬化が進行するものは使用することができな
い。この点の障害がなければ、絶縁性、パターン形成
性、密着性、強度、耐無電解メッキ性、耐電解メッキ性
等の工程適性など、ビルドアップ法による多層配線板に
必要な性能を満足する限り、使用される材料に制限は無
く、前記バインダーが使用できる。When a multi-layer film is used for the resin insulating layer, the multi-layer film is laminated on a wiring-formed base material. Can not do it. If there is no obstacle in this respect, the performance required for the multilayer wiring board by the build-up method, such as processability such as insulation property, pattern forming property, adhesion, strength, electroless plating resistance, and electroplating resistance, is satisfied. As long as the material used is not limited, the binder can be used.
【0034】第二の層の平均光学濃度分率をC、第一の
層の平均光学濃度分率をDとすると、CとDの比率(C
/D)は、好ましくは1.2から500、より好ましく
は2から200、最も好ましくは4から100である。
平均光学濃度の高い方が基板側になるように多層フィル
ムが基板に貼りつけられる。Assuming that the average optical density fraction of the second layer is C and the average optical density fraction of the first layer is D, the ratio of C to D (C
/ D) is preferably from 1.2 to 500, more preferably from 2 to 200, most preferably from 4 to 100.
The multilayer film is attached to the substrate such that the higher average optical density is on the substrate side.
【0035】第二の層の厚みは樹脂絶縁層全体の厚みの
約1/1000〜約1/2、1/200〜約1/5の範
囲、最も好ましくは1/100〜約1/10の範囲であ
る。The thickness of the second layer is in the range of about 1/1000 to about 1/2, 1/200 to about 1/5, and most preferably 1/100 to about 1/10 of the total thickness of the resin insulating layer. Range.
【0036】多層フィルムを形成するには、仮の支持体
上に第一の樹脂絶縁層を塗布し、別の仮の支持体上に第
二の樹脂絶縁層を塗布し、乾燥後にこれらを貼り合わせ
る。仮支持体としては、ポリエチレンテレフタレートフ
ィルム等のプラスチックフイルム、アルミ箔、銅箔、ニ
ッケル箔、ステンレス箔などの金属フィルムを用いるこ
とができる。プラスチックフィルムを仮支持体とする場
合は、フィルム形成後に、この仮支持体をカバーシート
として利用することができる。また、仮支持体をアルミ
箔にしておくと、仮の支持体が耐熱シートとなって、プ
レス機での貼り付け(比較的長い時間、高い温度に加熱
される)が可能となること、及び安価であることから、
好ましい。In order to form a multilayer film, a first resin insulating layer is applied on a temporary support, a second resin insulating layer is applied on another temporary support, and these are attached after drying. Match. As the temporary support, a plastic film such as a polyethylene terephthalate film, or a metal film such as an aluminum foil, a copper foil, a nickel foil, or a stainless steel foil can be used. When a plastic film is used as the temporary support, the temporary support can be used as a cover sheet after the film is formed. In addition, if the temporary support is made of aluminum foil, the temporary support becomes a heat-resistant sheet, and can be attached by a press (heated to a high temperature for a relatively long time), and Because it is cheap,
preferable.
【0037】仮支持体の膜厚は5〜100μmが適す
る。The thickness of the temporary support is suitably from 5 to 100 μm.
【0038】このような多層フィルムは配線パターンが
形成されたベース基板上に加熱、加圧圧着される。加
熱、加圧圧着には、ラミネーター、真空プレス機等のプ
レス機を用い、ポリプロピレン保護フィルム等があれ
ば、これを剥離し、樹脂絶縁層をむき出しにして行う。Such a multilayer film is heated and pressed under pressure on a base substrate on which a wiring pattern is formed. Pressing such as a laminator and a vacuum pressing machine is used for heating and pressure bonding. If there is a polypropylene protective film or the like, it is peeled off and the resin insulating layer is exposed.
【0039】樹脂絶縁層上には、メッキ等により配線が
設けられるが、一般に樹脂上にメッキをすると、メッキ
工程の途中でメッキが剥離したり、メッキ後のハンドリ
ング時にメッキが剥離することが多い。従って、樹脂絶
縁層の基板とは反対側の部分はその上にメッキを保持で
きることが必要である。このメッキ剥離は表面に凹凸を
設ける、表面をメッキ吸着性にする等により防止され
る。これらのメッキ剥離対策を行うために樹脂層に付与
する機能をメッキアンカー機能と呼ぶ。The wiring is provided on the resin insulating layer by plating or the like. In general, when plating is performed on the resin, the plating is often peeled off during the plating process, or the plating is often peeled off during handling after plating. . Therefore, it is necessary that the portion of the resin insulating layer opposite to the substrate can hold plating thereon. The peeling of the plating is prevented by providing irregularities on the surface or making the surface adsorbable by plating. The function imparted to the resin layer in order to perform these plating peeling measures is called a plating anchor function.
【0040】表面に凹凸を有する樹脂絶縁層を使用する
には、予め凹凸になった樹脂絶縁層を用いる場合と、後
から樹脂絶縁層に凹凸を設ける場合がある。In order to use a resin insulating layer having an uneven surface, there are a case where a resin insulating layer having an uneven surface is used in advance, and a case where an uneven surface is formed on the resin insulating layer later.
【0041】予め凹凸になった樹脂絶縁層の例として、
特開平9−244239号記載の予め粗面化された樹脂
フィルムを用いることが挙げられる。また、電解銅箔の
凹凸面に樹脂層を被覆して形成したフィルムを用いても
良い。ここで、本発明において「粗面化」とは、JIS
K5400に規定された方法に従って突出部の数を評
価し、5mmの間隔の碁盤目テストにおいて少なくとも
8点の突出部があることである。As an example of the resin insulating layer which has been made uneven in advance,
Use of a resin film which has been previously roughened as described in JP-A-9-244239 may be used. Further, a film formed by coating the resin layer on the uneven surface of the electrolytic copper foil may be used. Here, in the present invention, “roughening” refers to JIS
The number of protrusions is evaluated according to the method specified in K5400, and there is at least 8 protrusions in a grid test at intervals of 5 mm.
【0042】予め粗面化された樹脂フィルムは仮支持体
に樹脂層を塗布して作成される。該樹脂層に用いられる
樹脂としては、例えば、水に可溶な樹脂や膨潤し得る樹
脂から選ばれ、好ましくはポリビニルアルコール及びそ
の誘導体、ポリビニルピロリドン及びその誘導体、セル
ロース及びその誘導体、ゼラチン及びその誘導体、ポリ
アクリル酸及びその誘導体、スチレン/マレイン酸共重
合体のアミン変性物等が挙げられる。これらは単独で用
いても良いし、組み合わせて用いることもできる。The previously roughened resin film is prepared by applying a resin layer to a temporary support. The resin used for the resin layer is, for example, selected from water-soluble resins and swellable resins, preferably polyvinyl alcohol and its derivatives, polyvinylpyrrolidone and its derivatives, cellulose and its derivatives, gelatin and its derivatives , Polyacrylic acid and derivatives thereof, and amine-modified styrene / maleic acid copolymers. These may be used alone or in combination.
【0043】該樹脂層は微粒子を含有する。該微粒子
は、無機、有機低分子、あるいは有機高分子微粒子など
特に限定されないが、その好ましい例として、シリカ、
珪酸カルシウム、炭酸カルシウム、酸化亜鉛、酸化チタ
ン、ジルコニア、ムライト、水酸化カルシウム、タル
ク、水酸化アルミニウム、ケイソウ土、硫酸バリウム等
を挙げることができる。これらは単独で用いても良い
し、複数組み合わせて用いることも可能である。微粒子
の平均粒径もしくは凝集径は0.05〜10μmである
ことが好ましい。The resin layer contains fine particles. The fine particles are not particularly limited, such as inorganic, organic low molecular weight, or organic high molecular weight fine particles.
Examples thereof include calcium silicate, calcium carbonate, zinc oxide, titanium oxide, zirconia, mullite, calcium hydroxide, talc, aluminum hydroxide, diatomaceous earth, and barium sulfate. These may be used alone or in combination of two or more. The average particle diameter or aggregate diameter of the fine particles is preferably 0.05 to 10 μm.
【0044】該微粒子と樹脂の重量比は、0.5〜5位
の範囲が適当である。The weight ratio of the fine particles to the resin is suitably in the range of about 0.5 to 5.
【0045】このような微粒子を含有する樹脂溶液は、
通常樹脂を溶解した溶液もしくはメタノール等の溶剤と
水の混合溶液と微粒子を混合攪拌することにより得られ
る。微粒子の凝集サイズが大きい場合には、ホモジナイ
ザー等で強く攪拌したり、ペイントシェーカー等で分散
することも可能である。また予め、微粒子分散液と水性
樹脂を混合して得ることも可能であり、特に樹脂溶液の
調整法は限定されない。The resin solution containing such fine particles is as follows:
Usually, it is obtained by mixing and stirring a solution in which a resin is dissolved or a mixed solution of a solvent such as methanol and water and water and fine particles. When the aggregate size of the fine particles is large, it is also possible to stir vigorously with a homogenizer or the like, or to disperse them with a paint shaker or the like. In addition, it is also possible to obtain a fine particle dispersion liquid and an aqueous resin in advance, and the method for preparing the resin solution is not particularly limited.
【0046】また、該樹脂溶液には界面活性剤やマット
剤(微粒子)を添加したり、微粒子の沈降を防ぐ目的で
分散剤等を添加することも可能である。Further, a surfactant or a matting agent (fine particles) may be added to the resin solution, or a dispersant or the like may be added for the purpose of preventing sedimentation of the fine particles.
【0047】このような微粒子を含有する樹脂溶液はフ
ィルム上に塗布される。乾燥後の塗膜の膜厚は約0.2
〜15μmの範囲にすることが望ましい。The resin solution containing such fine particles is applied on a film. The film thickness after drying is about 0.2
It is desirable that the thickness be in the range of 15 μm.
【0048】後から凹凸を設ける方法として、特公平5
−55555(イビデン)のように、除去が容易な微粒
子を樹脂溶液に添加して樹脂絶縁層を形成しビアホール
形成後にこの微粒子を除去して表面を凹凸にすることが
挙げられる。As a method for providing irregularities later, Japanese Patent Publication No.
Addition of easily removable fine particles such as -55555 (Ibiden) to a resin solution to form a resin insulating layer, and removal of the fine particles after formation of via holes to make the surface uneven.
【0049】本発明では、ビアホールを光照射によって
形成するが、その方法には、レーザー照射法と、フォト
リソグラフィー法とがある。In the present invention, a via hole is formed by light irradiation. The method includes a laser irradiation method and a photolithography method.
【0050】レーザー照射法とは、固体レーザー(YA
Gレーザー、サファイアレーザーなど)、気体レーザー
(炭酸ガスレーザー、アルゴンイオンレーザー、ヘリウ
ム−ネオンレーザーなど)、半導体レーザー、色素レー
ザー、エキシマレーザー、自由電子レーザーなどによっ
て作られたレーザー光を樹脂絶縁層に照射することによ
って穴あけを行うもので、樹脂絶縁層はレーザーのエネ
ルギーによって分解除去される。ビアホールの形成にレ
ーザーを使用する場合、仮支持体の一部又は全部を剥離
する。The laser irradiation method refers to a solid laser (YA)
Laser light generated by G laser, sapphire laser, gas laser (carbon dioxide laser, argon ion laser, helium-neon laser, etc.), semiconductor laser, dye laser, excimer laser, free electron laser, etc. is applied to the resin insulation layer. Drilling is performed by irradiation, and the resin insulating layer is decomposed and removed by laser energy. When a laser is used to form a via hole, part or all of the temporary support is peeled off.
【0051】フォトリソグラフィー法とは、感光性を持
たせた樹脂絶縁層に画像様に光照射を行い(これを露光
と呼ぶ)、非照射部(又は光照射部)を現像で除去する
ことによってビアホールを形成する方法である。露光に
は、通常、フォトマスクを使用するが、フォトマスクを
使用しないでレーザー光など、細く絞られた光をスキャ
ニングしてもよい。The photolithography method is to irradiate a photosensitive resin-insulating layer imagewise with light (this is called exposure) and remove the non-irradiated portion (or light-irradiated portion) by development. This is a method of forming a via hole. A photomask is usually used for the exposure, but finely narrowed light such as laser light may be scanned without using the photomask.
【0052】本発明では、生産性が高いことからフォト
リソグラフィー法がより好ましい。In the present invention, a photolithography method is more preferable because of high productivity.
【0053】ビアホールの形成がフォトリソグラフィー
法の場合、露光の際に仮支持体をそのままにしても良い
し、剥離してもよい。高解像度が必要な場合は、仮支持
体を剥離して露光することが望ましい。または仮支持体
として2枚の支持体の貼りあわせ品を用い、露光前に厚
い方の支持体を剥離しても良い。When the via hole is formed by photolithography, the temporary support may be left as it is or may be peeled off at the time of exposure. When high resolution is required, it is desirable that the temporary support be peeled off and exposed. Alternatively, a laminated product of two supports may be used as a temporary support, and the thicker support may be peeled off before exposure.
【0054】露光には超高圧水銀灯等を用いることがで
き、拡散光、平行光のいずれも使用できる。An ultra-high pressure mercury lamp or the like can be used for exposure, and either diffused light or parallel light can be used.
【0055】フォトリソグラフィー法の場合、次に溶剤
又はアルカリ水溶液により現像を行い、ビアホールを形
成する。現像液が溶剤の場合はクロロセン等のクロル系
溶剤等を用い、アルカリ水溶液の場合には現像主剤とし
ての0.3〜2%程度の炭酸ナトリウム、水酸化ナトリ
ウム、水酸化カリウム、トリエタノールイミン、ジエタ
ノールアミンあるいはテトラメチルアンモニウムハイド
ロキサイド等を溶解した水溶液を用いることができる。In the case of the photolithography method, development is performed with a solvent or an aqueous alkali solution to form a via hole. When the developing solution is a solvent, a chloro-based solvent such as chlorocene is used. When the developing solution is an alkaline aqueous solution, about 0.3 to 2% of sodium carbonate, sodium hydroxide, potassium hydroxide, triethanolimine as a developing agent is used. An aqueous solution in which diethanolamine or tetramethylammonium hydroxide is dissolved can be used.
【0056】アルカリ水溶液系現像液には必要に応じ
て、界面活性剤やベンジルアルコールのような溶剤を添
加することもできる。現像法としてはシャワー現像やブ
ラシ現像、あるいは両者を組み合わせた方法を用いるこ
とができる。If necessary, a surfactant or a solvent such as benzyl alcohol can be added to the alkaline aqueous solution-based developer. As a developing method, shower developing, brush developing, or a method combining both can be used.
【0057】現像終了後、20℃〜200℃の温度でポ
ストベイクを行うことが望ましい。After the development is completed, it is desirable to perform post-baking at a temperature of 20 ° C. to 200 ° C.
【0058】前記現像液が入った現像浴での現像の後、
基板は水洗浴で水洗されるが、微細なビアホールを確実
に形成するには、現像浴と水洗浴の間に補助処理浴での
処理工程を設けることが好ましい。After development in a developing bath containing the developer,
Although the substrate is washed with a washing bath, it is preferable to provide a processing step in an auxiliary treatment bath between the developing bath and the washing bath in order to surely form fine via holes.
【0059】補助処理浴には塩酸、硫酸、過硫酸アンモ
ニウム、過硫酸ナトリウム等の酸の水溶液、あるいは水
酸化ナトリウム等の水溶液を用いる。For the auxiliary treatment bath, an aqueous solution of an acid such as hydrochloric acid, sulfuric acid, ammonium persulfate, or sodium persulfate, or an aqueous solution of sodium hydroxide or the like is used.
【0060】以上により1〜100μm、好ましくは2
〜60μm、より好ましくは4〜40μmの、ビアホー
ルを形成することができる。また、本発明により形成さ
れるビアホールの密度は0.5〜200個/mm2であ
り、好ましくは1〜150個/mm2、より好ましくは
5〜120個/mm2である。As described above, 1 to 100 μm, preferably 2 μm
Via holes of up to 60 μm, more preferably 4 to 40 μm can be formed. The density of via holes formed according to the present invention is 0.5 to 200 holes / mm 2 , preferably 1 to 150 holes / mm 2 , and more preferably 5 to 120 holes / mm 2 .
【0061】以上のようなビアホールを有する樹脂絶縁
層の上に、無電解銅メッキ、電解銅メッキ等が施され、
配線となる。Electroless copper plating, electrolytic copper plating, or the like is performed on the resin insulating layer having the above via holes,
It becomes wiring.
【0062】上記工程を繰り返すことにより、多層配線
が形成される。By repeating the above steps, a multilayer wiring is formed.
【0063】[0063]
【実施例】以下、実施例により、本発明を更に詳細に説
明するが、本発明はこれらに限定されるものではない。
実施例1 (1)多層フィルムの作製 仮の支持体として厚さ20μmのポリエチレンテレフタ
レート(PET)フィルム上に、下記組成の簡易粗面化
用樹脂溶液をホモジナイザーにて分散後、6μmの膜厚
になるよう塗布し、塗膜を100℃で10分間乾燥し
た。EXAMPLES The present invention will be described in more detail with reference to the following Examples, but it should not be construed that the present invention is limited thereto.
Example 1 (1) Production of Multilayer Film A resin solution for simple surface roughening having the following composition was dispersed on a polyethylene terephthalate (PET) film having a thickness of 20 μm as a temporary support with a homogenizer, and then the thickness was reduced to 6 μm. And dried at 100 ° C. for 10 minutes.
【0064】塗布品は白濁しており、SEMで表面の凹
凸が観察された。 <簡易粗面化用樹脂溶液の組成> ・ポリビニルアルコールPVA205(クラレ社製) 37.5 重量部 ・ポリビニルピロリドンK30(信越化学社製) 18.75重量部 ・ヒドロキシプロピルメチルセルロースTC5E(五協産業社製〉 37.50重量部 ・炭酸カルシウム(白石工業株式会社)を気相粉砕し平均粒径を2μmとした もの 26.9 重量部 ・フッ素系界面活性剤サーフロンS131(旭ガラス社製) 0.2 重量部 ・純水 97.8 重量部 次に下記組成の樹脂溶液A、Bを、エクストロージョン
型2段ギーサーを用いて、上記塗布品の白濁した層の上
に同時に重層塗布し、カバーシートとしてポリエチレン
(PE)フィルムを貼り付けながら得られたフィルムを
巻き取った。The coated product was cloudy, and surface irregularities were observed by SEM. <Composition of the resin solution for simple roughening> ・ 37.5 parts by weight of polyvinyl alcohol PVA205 (manufactured by Kuraray) ・ 18.75 parts by weight of polyvinylpyrrolidone K30 (manufactured by Shin-Etsu Chemical Co., Ltd.) ・ Hydroxypropylmethylcellulose TC5E (gokyo industry) 37.50 parts by weight-Calcium carbonate (Shiraishi Kogyo Co., Ltd.) vapor-phase crushed to an average particle size of 2 µm 26.9 parts by weight-Fluorosurfactant Surflon S131 (manufactured by Asahi Glass Co., Ltd.) 2 parts by weight ・ Pure water 97.8 parts by weight Next, resin solutions A and B having the following composition were simultaneously applied on the cloudy layer of the above-mentioned coated product using an extrusion-type two-stage Gieser to form a cover sheet. The obtained film was wound up while attaching a polyethylene (PE) film.
【0065】乾燥後の樹脂絶縁層Aの膜厚は16μm、
樹脂絶縁層Bの膜厚は2μmであった。これらの値は、
前記粗面化用樹脂液を塗布していない部分に塗布した樹
脂絶縁層A、Bを切断し、断面の各層の厚みを光学顕微
鏡により測定した。The thickness of the resin insulating layer A after drying is 16 μm,
The thickness of the resin insulating layer B was 2 μm. These values are
The resin insulating layers A and B applied to portions where the surface-roughening resin solution was not applied were cut, and the thickness of each layer in the cross section was measured with an optical microscope.
【0066】乾燥後の樹脂絶縁層A、Bの光学濃度分率
はそれぞれ0.0125、0.4であった。それぞれの
光学濃度分率は、樹脂絶縁層Aを支持体に単独で設け、
乾燥後剥離した塗膜の測定により樹脂絶縁層Aの光学濃
度を求め、次に支持体に樹脂絶縁層A、Bを同時重層塗
布後乾燥して樹脂絶縁層A、Bを一体的に剥離した塗膜
の光学濃度を測定することにより樹脂絶縁層A、Bの光
学濃度の合計を求め、これを基に、計算で求めた。 <Aの樹脂溶液組成> ・バインダー[スチレン/マレイン酸ベンジルアミン変性物/メタクロイルオ キシエチルジフェニルホスフェー卜共重合体(40/32/28(モル比))、 固形分量36重量%、残り成分メチルエチルケトン、分子量3万] 50 重量部 ・2,2−ジメトキシ−1,2−ジフェニルエタン−1−オン 2.15 重量部 ・フェニドン 0.0056重量部 ・シクロヘキサノン 17.4 重量部 ・DPHA(日本化薬(株)製多官能モノマー) 9.03 重量部 ・R−712(日本化薬(株)製) 6.77 重量部 ・M−315(日本化薬(株)製) 6.77 重量部 <Bの樹脂溶液組成> ・バインダー[スチレン/マレイン酸ベンジルアミン変性物/メタクロイルオ キシエチルジフェニルホスフェート共重合体(28/44/28(モル比))、 固形分量31重量%、残り成分メチルエチルケトン、分子量3万] 50 重量部 ・2,2−ジメトキシ−1,2−ジフェニルエタン−1−オン 1.49 重量部 ・フェニドン 0.0039重量部 ・フッ素系界面活性剤サーフロンS131 1.720 重量部 ・メチルエチルケトン 83 重量部 ・シクロヘキサノン 55 重量部 ・DPHA 6.22 重量部 ・R−712 4.67 重量部 ・M−315 4.67 重量部 ・顔料(C.I.=PB15:6) 3.48 重量部 (ベース基板へのラミネート)ベース基板として表面に
厚み8μmのBO(ブラックオキサイド)ハロレス処理
の銅配線を有すガラスエポキシ基板の両面に、カバーシ
ート(PEフィルム)を剥離した上記多層フィルムを、
真空ラミネーター(30秒で3hPaまで減圧後、10
0℃の熱板を30秒間5000hPaで圧着)により樹
脂絶縁層Bが基板側になるようにラミネートした。The optical density fractions of the dried resin insulating layers A and B were 0.0125 and 0.4, respectively. Each optical density fraction is provided by providing the resin insulating layer A alone on the support,
The optical density of the resin insulating layer A was determined by measuring the coating film that was peeled off after drying, and then the resin insulating layers A and B were simultaneously coated on the support and dried, and then the resin insulating layers A and B were integrally peeled off. By measuring the optical density of the coating film, the sum of the optical densities of the resin insulating layers A and B was obtained, and the total was calculated based on this. <Resin solution composition of A> Binder [styrene / benzylamine maleate modified product / methacryloyloxyethyldiphenyl phosphate copolymer (40/32/28 (molar ratio)), solid content 36% by weight, remaining component methyl ethyl ketone , Molecular weight 30,000] 50 parts by weight ・ 2,2-dimethoxy-1,2-diphenylethan-1-one 2.15 parts by weight ・ Phenidone 0.0056 parts by weight ・ Cyclohexanone 17.4 parts by weight ・ DPHA (Nippon Kayaku 9.03 parts by weight R-712 (manufactured by Nippon Kayaku Co., Ltd.) 6.77 parts by weight M-315 (manufactured by Nippon Kayaku Co., Ltd.) 6.77 parts by weight < B. Resin Solution Composition> Binder [styrene / benzylamine maleate modified product / methacryloyloxyethyldiphenyl phosphate copolymer (28 / 44/28 (molar ratio)), solid content 31% by weight, remaining component methyl ethyl ketone, molecular weight 30,000] 50 parts by weight • 2,2-dimethoxy-1,2-diphenylethan-1-one 1.49 parts by weight • Phenidone 0.0039 parts by weight-Fluorosurfactant Surflon S131 1.720 parts by weight-Methyl ethyl ketone 83 parts by weight-Cyclohexanone 55 parts by weight-DPHA 6.22 parts by weight-R-712 4.67 parts by weight-M-315 4 .67 parts by weight ・ Pigment (CI = PB15: 6) 3.48 parts by weight (lamination on base substrate) Glass having 8 μm thick BO (black oxide) haloless-treated copper wiring on the surface as a base substrate On both sides of the epoxy substrate, the above multilayer film from which the cover sheet (PE film) was peeled off,
Vacuum laminator (After reducing the pressure to 3 hPa in 30 seconds, 10
A hot plate at 0 ° C. was pressed for 30 seconds at 5000 hPa) so that the resin insulating layer B was on the substrate side.
【0067】配線上の樹脂絶縁層の総厚みは16μm、
粗面化層の厚み2μm、樹脂絶縁層Aの厚み12μm、
樹脂絶縁層Bの厚み2μmであった。The total thickness of the resin insulating layer on the wiring is 16 μm,
The thickness of the roughened layer is 2 μm, the thickness of the resin insulating layer A is 12 μm,
The thickness of the resin insulating layer B was 2 μm.
【0068】厚み方向でベース基板側の半分の平均光学
濃度分率は0.1、ベース基板と半体側の半分の平均光
学濃度分率は0.0125、両者の比は8であった。 (露光)ビアホールの密度が10個/mm2のマスクを
用い平行光で30mJ/cm2の露光量でパターン露光
を行った。 (現像)仮の支持体(PETフイルム)を剥離後、40
℃に温度調節した2.8重量%トリエタノールアミン水
溶液を圧力1500hPaで70秒間基板の両面に噴射
してシャワー現像を行った。引き続き室温の12重量%
過硫酸アンモニウム水溶液を圧力1500hPaで60
秒間シャワー噴射し、さらに引き続き、室温の水を圧力
1500hPaで60秒間シャワー噴射し、60℃の温
風で基板を乾燥した。この結果、直径30μmのビアホ
ールが形成され、また樹脂層表面に凹凸が形成された。 (ポストベイク)160℃で60分基板を加熱し、樹脂
層を完全に硬化して絶縁層とした。 (メッキ)次にメルテックス社製の処理剤を用い、以下
の手順で、無電解銅メッキまでを行った。In the thickness direction, the average optical density fraction of the half on the base substrate side was 0.1, the average optical density fraction of the half on the base substrate half and the half was 0.0125, and the ratio between the two was 8. (Exposure) Using a mask having a via hole density of 10 holes / mm 2 , pattern exposure was performed with parallel light at an exposure amount of 30 mJ / cm 2 . (Development) After removing the temporary support (PET film),
A 2.8% by weight aqueous solution of triethanolamine adjusted to a temperature of ° C. was sprayed onto both surfaces of the substrate at a pressure of 1500 hPa for 70 seconds to perform shower development. 12% by weight of room temperature
An aqueous solution of ammonium persulfate is applied at a pressure of 1500 hPa for 60 hours.
Shower spray was performed for 60 seconds, and then water at room temperature was shower-sprayed at a pressure of 1500 hPa for 60 seconds, and the substrate was dried with hot air at 60 ° C. As a result, a via hole having a diameter of 30 μm was formed, and irregularities were formed on the surface of the resin layer. (Post bake) The substrate was heated at 160 ° C. for 60 minutes to completely cure the resin layer to form an insulating layer. (Plating) Next, using a treatment agent manufactured by Meltex Co., the process up to electroless copper plating was performed in the following procedure.
【0069】前処理剤(PC236)に25℃で3分間
基板を浸漬し、その後2分間純水で水洗した。次いで、
触媒付与剤(アクチベーター444)に25℃で6分間
基板を浸漬し、その後2分間純水で水洗した。次に、活
性化処理剤(PA491)に25℃で6分間基板を浸漬
し、その後2分間純水で水洗した。次いで、無電解銅メ
ッキ液(CU390)に25℃、pH12.9の条件下
10分間基板を浸漬し、その後純水で5分間水洗した。
水洗後基板を100℃で15分乾燥した。この結果、膜
厚約0.3μmの無電解銅メッキ膜が形成された。The substrate was immersed in a pretreatment agent (PC236) at 25 ° C. for 3 minutes, and then washed with pure water for 2 minutes. Then
The substrate was immersed in a catalyst imparting agent (activator 444) at 25 ° C. for 6 minutes, and then washed with pure water for 2 minutes. Next, the substrate was immersed in an activating agent (PA491) at 25 ° C. for 6 minutes, and then washed with pure water for 2 minutes. Next, the substrate was immersed in an electroless copper plating solution (CU390) at 25 ° C. and a pH of 12.9 for 10 minutes, and then washed with pure water for 5 minutes.
After washing with water, the substrate was dried at 100 ° C. for 15 minutes. As a result, an electroless copper plating film having a thickness of about 0.3 μm was formed.
【0070】引き続き、メルテックス社製の脱脂処理剤
(PC455)に25℃で30秒基板を浸漬し、2分間
水洗後、電解銅メッキを行った。電解銅メッキ液は硫酸
銅75g/リットル、硫酸190g/リットル、塩素イ
オン約50ppm、及びメルテックス社製カパーグリー
ムPCM5ml/リットルの組成物で、25℃、2.5
A/100cm2、24分の条件で基板の両面にメッキ
を行った。この結果、約12μmの銅が析出した。次に
基板をオーブンに入れ、160℃で60分放置後、ドラ
イフィルムレジストを用い、銅のエッチングを行い、配
線及び層間接続部を形成した。これをBOハロレス処理
し、厚さ8μの配線を得た。Subsequently, the substrate was immersed in a degreasing agent (PC455) manufactured by Meltex Corporation at 25 ° C. for 30 seconds, washed with water for 2 minutes, and then subjected to electrolytic copper plating. The electrolytic copper plating solution is a composition of copper sulfate 75 g / l, sulfuric acid 190 g / l, chlorine ion about 50 ppm, and Copperglyme PCM 5 ml / l manufactured by Meltex Co., Ltd.
Plating was performed on both sides of the substrate under the conditions of A / 100 cm 2 for 24 minutes. As a result, about 12 μm of copper was deposited. Next, the substrate was placed in an oven, left at 160 ° C. for 60 minutes, and then copper was etched using a dry film resist to form wirings and interlayer connections. This was subjected to BO haloless treatment to obtain an 8 μm thick wiring.
【0071】更に、この上に多層フィルムをラミネート
して、前記と同様にして第3層目の配線を形成した。 (半田耐熱試験)260℃、20秒間の半田耐熱試験を
行ったところ、ビアホールの接続不良は発生しなかっ
た。比較例1 樹脂溶液Bを用いない(樹脂溶液Aの単層を設ける)他
は実施例1と同様にして多層フィルムを作成し、これを
用いた多層配線基板を作成した。Further, a multilayer film was laminated thereon, and a third-layer wiring was formed in the same manner as described above. (Solder Heat Resistance Test) When a solder heat resistance test was performed at 260 ° C. for 20 seconds, no connection failure of the via hole occurred. Comparative Example 1 A multilayer film was prepared in the same manner as in Example 1 except that the resin solution B was not used (a single layer of the resin solution A was provided), and a multilayer wiring board was prepared using the multilayer film.
【0072】配線上の樹脂絶縁層の総厚みは16μm、
粗面化層の厚み2μm 樹脂絶縁層Aの厚み14μmで
あった。The total thickness of the resin insulating layer on the wiring is 16 μm,
The thickness of the roughened layer was 2 μm. The thickness of the resin insulating layer A was 14 μm.
【0073】厚み方向でベース基板側の半分の平均光学
濃度分率は0.0125、ベース基板と反対側の半分の
平均光学濃度分率は0.0125、両者の比は1であっ
た。In the thickness direction, the average optical density fraction of the half on the base substrate side was 0.0125, the average optical density fraction of the half on the side opposite to the base substrate was 0.0125, and the ratio between the two was 1.
【0074】半田耐熱試験後のビアホールの接続不良率
は32%であった。The defective connection rate of the via hole after the soldering heat test was 32%.
【0075】[0075]
【発明の効果】本発明は、樹脂絶縁層の上下の平均光学
濃度分率の比を所定の範囲にしたので、直径が100μ
m以下のビアホールを有する多層配線基板でのビアホー
ルの接続不良を改善できる。According to the present invention, the ratio of the average optical density fraction above and below the resin insulating layer is within a predetermined range, so that the diameter of the resin insulating layer is 100 μm.
It is possible to improve poor connection of via holes in a multilayer wiring board having via holes of not more than m.
───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 2H025 AA00 AA02 AB15 AB17 AB20 AC01 AC08 AD01 BC13 BC31 DA11 DA20 DA21 DA40 FA17 FA43 2H096 AA27 BA05 CA01 EA02 EA04 HA27 5E346 AA12 AA16 AA38 AA43 BB01 CC08 DD02 DD03 EE31 FF04 GG15 HH07 ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 2H025 AA00 AA02 AB15 AB17 AB20 AC01 AC08 AD01 BC13 BC31 DA11 DA20 DA21 DA40 FA17 FA43 2H096 AA27 BA05 CA01 EA02 EA04 HA27 5E346 AA12 AA16 AA38 AA43 BB01 CC08 DD02 DD03 GG31 EE31
Claims (3)
濃度分率が、他方の面から半分の厚みまでの平均光学濃
度分率の1.2倍から500倍であり、平均光学濃度分
率の低い方の面がその上にメッキ層を保持することが可
能である樹脂絶縁層の平均光学濃度分率が低い方の面か
ら光を照射して画像を形成することを特徴とする画像形
成方法。The average optical density fraction from one surface to half the thickness is 1.2 to 500 times the average optical density fraction from the other surface to half the thickness. An image characterized in that an image is formed by irradiating light from a surface having a lower average optical density fraction of a resin insulating layer on which a surface having a lower ratio can hold a plating layer thereon. Forming method.
とも2層の配線と少なくとも1層の樹脂絶縁層が形成さ
れるように配線と樹脂絶縁層とが交互に配置され、上下
の配線を電気的に接続するビアホールが樹脂絶縁層に形
成された多層配線基板であって、 各樹脂絶縁層の基板側の面から層の半分の厚みまでの平
均光学濃度分率が該絶縁層の基板と反対側の面から層の
半分の厚みまでの平均光学濃度分率の1.2倍から50
0倍である多層配線基板。2. Wiring and resin insulating layers are alternately arranged on at least one surface of a base substrate so that at least two wirings and at least one resin insulating layer are formed, and upper and lower wirings are electrically connected. A multilayer wiring board in which via holes to be connected are formed in a resin insulating layer, wherein the average optical density fraction from the substrate side surface of each resin insulating layer to half the thickness of the layer is the opposite of the insulating layer from the substrate. 1.2 times to 50 times the average optical density fraction from the surface to half the thickness of the layer
Multilayer wiring board that is 0x.
一の樹脂絶縁層と第二の樹脂絶縁層からなり、第一の樹
脂絶縁層がその上にメッキ層を保持することが可能であ
り、第二の樹脂絶縁層の平均光学濃度分率が第一の樹脂
絶縁層の平均光学濃度分率の1.2倍から500倍であ
る多層フィルム。3. A first resin insulating layer and a second resin insulating layer capable of forming a via hole by light irradiation, wherein the first resin insulating layer can hold a plating layer thereon. A multilayer film in which the average optical density fraction of the second resin insulating layer is 1.2 to 500 times the average optical density fraction of the first resin insulating layer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11172421A JP2001005178A (en) | 1999-06-18 | 1999-06-18 | Image forming method, multilayer circuit board, and multilayer film used for the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11172421A JP2001005178A (en) | 1999-06-18 | 1999-06-18 | Image forming method, multilayer circuit board, and multilayer film used for the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2001005178A true JP2001005178A (en) | 2001-01-12 |
Family
ID=15941666
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11172421A Pending JP2001005178A (en) | 1999-06-18 | 1999-06-18 | Image forming method, multilayer circuit board, and multilayer film used for the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2001005178A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002025377A1 (en) * | 2000-09-20 | 2002-03-28 | Hitachi Chemical Co., Ltd. | Photosensitive element, method for forming resist pattern, and method for manufacturing printed wiring board |
| WO2006011548A1 (en) * | 2004-07-30 | 2006-02-02 | Hitachi Chemical Company, Ltd. | Photosensitive film, photosensitive film laminate and photosensitive film roll |
| JP2008065312A (en) * | 2006-07-19 | 2008-03-21 | E I Du Pont De Nemours & Co | Flame retardant multilayer photoimageable coverlay compositions and related methods |
-
1999
- 1999-06-18 JP JP11172421A patent/JP2001005178A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002025377A1 (en) * | 2000-09-20 | 2002-03-28 | Hitachi Chemical Co., Ltd. | Photosensitive element, method for forming resist pattern, and method for manufacturing printed wiring board |
| US7078151B2 (en) | 2000-09-20 | 2006-07-18 | Hitachi Chemical Co., Ltd. | Photosensitive element, method for forming resist pattern, and method for manufacturing printed wiring board |
| WO2006011548A1 (en) * | 2004-07-30 | 2006-02-02 | Hitachi Chemical Company, Ltd. | Photosensitive film, photosensitive film laminate and photosensitive film roll |
| JP2008065312A (en) * | 2006-07-19 | 2008-03-21 | E I Du Pont De Nemours & Co | Flame retardant multilayer photoimageable coverlay compositions and related methods |
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