JP2023010737A - 樹脂組成物 - Google Patents
樹脂組成物 Download PDFInfo
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- JP2023010737A JP2023010737A JP2022173670A JP2022173670A JP2023010737A JP 2023010737 A JP2023010737 A JP 2023010737A JP 2022173670 A JP2022173670 A JP 2022173670A JP 2022173670 A JP2022173670 A JP 2022173670A JP 2023010737 A JP2023010737 A JP 2023010737A
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- resin
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- epoxy resin
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- 238000000790 scattering method Methods 0.000 description 1
- 125000005920 sec-butoxy group Chemical group 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229910000018 strontium carbonate Inorganic materials 0.000 description 1
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 description 1
- TXDNPSYEJHXKMK-UHFFFAOYSA-N sulfanylsilane Chemical compound S[SiH3] TXDNPSYEJHXKMK-UHFFFAOYSA-N 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 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
- 150000003512 tertiary amines Chemical class 0.000 description 1
- GHPYAGKTTCKKDF-UHFFFAOYSA-M tetraphenylphosphanium;thiocyanate Chemical compound [S-]C#N.C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 GHPYAGKTTCKKDF-UHFFFAOYSA-M 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical class SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- JLGNHOJUQFHYEZ-UHFFFAOYSA-N trimethoxy(3,3,3-trifluoropropyl)silane Chemical compound CO[Si](OC)(OC)CCC(F)(F)F JLGNHOJUQFHYEZ-UHFFFAOYSA-N 0.000 description 1
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000004506 ultrasonic cleaning Methods 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
- 229910000166 zirconium phosphate Inorganic materials 0.000 description 1
- LEHFSLREWWMLPU-UHFFFAOYSA-B zirconium(4+);tetraphosphate Chemical compound [Zr+4].[Zr+4].[Zr+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LEHFSLREWWMLPU-UHFFFAOYSA-B 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- C09D179/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen, or carbon only, not provided for in groups C09D161/00 - C09D177/00
- C09D179/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C09D179/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
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- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
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- C—CHEMISTRY; METALLURGY
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
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- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
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Abstract
Description
[1] (A)エポキシ樹脂、(B)硬化剤、及び(C)ポリイミド樹脂を含む樹脂組成物であって、(B)成分が、(B-1)3官能以上のマレイミド化合物を含む、樹脂組成物。
[2] (B-1)成分が、式(B1):
で表される化合物である、上記[1]に記載の樹脂組成物。
[3] (B)成分の含有量が、樹脂組成物中の不揮発成分を100質量%としたとき、1質量%~40質量%である、上記[1]又は[2]に記載の樹脂組成物。
[4] (B)成分に対する(B-1)成分の質量割合が、樹脂組成物中の(B)成分を100質量%としたとき、10質量%以上である、上記[1]~[3]の何れかに記載の樹脂組成物。
[5] さらに(D)無機充填材を含み又は含まず、(D)成分の含有量が、樹脂組成物中の不揮発成分を100質量%としたとき、70質量%以下である、上記[1]~[4]の何れかに記載の樹脂組成物。
[6] さらに(D)無機充填材を含む、上記[1]~[5]の何れかに記載の樹脂組成物。
[7] 25℃から150℃におけるZ方向の線熱膨張係数が、100ppm以下である、上記[1]~[6]の何れかに記載の樹脂組成物。
[8] 多層フレキシブル基板の絶縁層形成用である、上記[1]~[7]の何れかに記載の樹脂組成物。
[9] 上記[1]~[8]の何れかに記載の樹脂組成物の硬化物。
[10] 支持体と、当該支持体上に設けられた上記[1]~[8]の何れかに記載の樹脂組成物で形成された樹脂組成物層とを含む、樹脂シート。
[11] 上記[1]~[8]の何れかに記載の樹脂組成物を硬化して形成される絶縁層を含む多層フレキシブル基板。
[12] 上記[11]に記載の多層フレキシブル基板を備える、半導体装置。
本発明の樹脂組成物は、(A)エポキシ樹脂、(B)硬化剤、及び(C)ポリイミド樹脂を含む。(B)成分は、(B-1)3官能以上のマレイミド化合物を含む。
本発明の樹脂組成物は、(A)エポキシ樹脂を含有する。
本発明の樹脂組成物は、(B)硬化剤を含有する。(B)硬化剤は、(A)エポキシ樹脂を硬化する機能を有する。
(B-1)3官能以上のマレイミド化合物とは、2,5-ジヒドロ-2,5-ジオキソ-1H-ピロール-1-イル基(いわゆるマレイミド基)を3個以上有する化合物を意味する。(B-1)3官能以上のマレイミド化合物は、特に限定されるものではないが、例えば、式(B1):
で表される化合物が好ましい。
(B)硬化剤は、(B-1)3官能以上のマレイミド化合物に加えて、さらにその他の硬化剤を含んでいてもよい。(B-1)成分以外のその他の硬化剤としては、エポキシ樹脂を硬化する機能を有する限り特に限定されず、例えば、2官能のマレイミド化合物、フェノール系硬化剤、ナフトール系硬化剤、酸無水物系硬化剤、活性エステル系硬化剤、ベンゾオキサジン系硬化剤、シアネートエステル系硬化剤及びカルボジイミド系硬化剤が挙げられる。このような硬化剤は1種単独で用いてもよく、2種以上を組み合わせて用いてもよい。
本発明の樹脂組成物は、(C)ポリイミド樹脂を含有する。(C)ポリイミド樹脂は、繰り返し単位中にイミド結合を持つ樹脂であれば特に限定されない。(C)ポリイミド樹脂は、一般に、ジアミン化合物と酸無水物とのイミド化反応により得られる樹脂を含み得る。(C)ポリイミド樹脂には、シロキサン変性ポリイミド樹脂などの変性ポリイミド樹脂も含まれる。
等が挙げられる。
で表されるジアミン化合物等が挙げられる。
で表される化合物であり、より好ましくは、式(1’’):
で表される化合物が挙げられる。
本発明の樹脂組成物は、任意成分として(D)無機充填材を含む場合がある。
本発明の樹脂組成物は、任意成分として(E)硬化促進剤を含む場合がある。
本発明の樹脂組成物は、任意の揮発性成分として、さらに(F)有機溶剤を含有する場合がある。
樹脂組成物は、上述した成分以外に、任意の成分として、更にその他の添加剤を含んでいてもよい。このような添加剤としては、例えば、有機充填剤、増粘剤、消泡剤、レベリング剤、密着性付与剤、重合開始剤、難燃剤などが挙げられる。これらの添加剤は、1種類単独で用いてもよく、2種類以上を組み合わせて用いてもよい。それぞれの含有量は当業者であれば適宜設定できる。
一実施形態において、本発明の樹脂組成物は、例えば、反応容器に(A)エポキシ樹脂、(B)硬化剤、(C)ポリイミド樹脂(予めイミド化されているもの)、必要に応じて(D)無機充填材、必要に応じて(E)硬化促進剤、必要に応じて(F)有機溶剤、及び必要に応じて(G)その他の添加剤を、任意の順で及び/又は一部若しくは全部同時に加えて混合し、樹脂組成物を得る工程(以下、工程(1)という)を含む方法によって、製造することができる。
本発明の樹脂組成物は、(A)エポキシ樹脂、(B)硬化剤、及び(C)ポリイミド樹脂を含み、(B)成分が、(B-1)3官能以上のマレイミド化合物を含むため、Z方向(層状硬化物を得た場合の厚さ方向)の線熱膨張係数が低く且つ柔軟性に優れた硬化物を得ることができる。
本発明の樹脂シートは、支持体と、該支持体上に設けられた、本発明の樹脂組成物で形成された樹脂組成物層を含む。
積層シートは、複数の樹脂シートを積層及び硬化して製造されるシートである。よって、積層シートは、樹脂シートの硬化物としての絶縁層を複数含む。通常、積層シートを製造するために積層される樹脂シートの数は、積層シートに含まれる絶縁層の数に一致する。積層シート1枚当たりの具体的な絶縁層の数は、通常2以上、好ましくは3以上、特に好ましくは5以上であり、好ましくは20以下、より好ましくは15以下、特に好ましくは10以下である。
積層シートは、(a)樹脂シートを準備する工程、並びに、(b)樹脂シートを複数積層及び硬化する工程、を含む製造方法によって、製造できる。樹脂シートの積層及び硬化の順番は、所望の積層シートが得られる限り、任意である。例えば、複数の樹脂シートを全て積層した後で、積層された複数の樹脂シートを一括して硬化させてもよい。また、例えば、ある樹脂シートに別の樹脂シートを積層する都度、その積層された樹脂シートの硬化を行ってもよい。
(II)第一樹脂シートを硬化して、第一絶縁層を形成する工程と、
(VI)第一絶縁層に、第二樹脂シートを積層する工程と、
(VII)第二樹脂シートを硬化して、第二絶縁層を形成する工程と、
を含む。また、工程(b)は、必要に応じて、
(I)シート支持基材に第一樹脂シートを積層する工程、
(III)第一絶縁層に、穴あけする工程、
(IV)第一絶縁層に粗化処理を施す工程、
(V)第一絶縁層上に導体層を形成する工程
等の任意の工程を含んでいてもよい。以下、各工程について説明する。
多層フレキシブル基板は、積層シートを含む。したがって、多層フレキシブル基板は、本発明の樹脂組成物を硬化して形成される絶縁層を含む。多層フレキシブル基板は、積層シートのみを含んでいてもよく、積層シートに組み合わせて任意の部材を含んでいてもよい。任意の部材としては、例えば、電子部品、カバーレイフィルムなどが挙げられる。
半導体装置は、前記の多層フレキシブル基板を備える。半導体装置は、例えば、多層フレキシブル基板と、この多層フレキシブル基板に実装された半導体チップとを備える。多くの半導体装置では、多層フレキシブル基板は、半導体装置の筐体に、その多層フレキシブル基板が含む積層シートの一方の面が向かい合うように折り曲げて収納され得る。
窒素導入管、撹拌装置を備えた500mlセパラブルフラスコに、4-アミノ安息香酸5-アミノ-1,1’-ビフェニル-2-イル(式(1’’)の化合物)9.13g(30ミリモル)、4,4’-(4,4’-イソプロピリデンジフェノキシ)ビスフタル酸二無水物15.61g(30ミリモル)、N-メチル-2-ピロリドン94.64g、ピリジン0.47g(6ミリモル)、トルエン10gを投入し、窒素雰囲気下、180℃で、途中トルエンを系外にのぞきながら4時間イミド化反応させることにより、ポリイミド樹脂1を含むポリイミド溶液(不揮発分20質量%)を得た。ポリイミド溶液において、合成したポリイミド樹脂1の析出は見られなかった。
撹拌機、分水器、温度計及び窒素ガス導入管を備えた反応容器に、芳香族テトラカルボン酸二無水物(SABICジャパン社製「BisDA-1000」、4,4’-(4,4’-イソプロピリデンジフェノキシ)ビスフタル酸二無水物)65.0g、シクロヘキサノン266.5g、及びメチルシクロヘキサン44.4gを仕込み、溶液を60℃まで加熱した。次いで、ダイマージアミン(クローダジャパン社製「PRIAMINE 1075」)43.7g、及び1,3-ビス(アミノメチル)シクロヘキサン5.4gを滴下した後、140℃で1時間かけてイミド化反応させた。これにより、ポリイミド樹脂2を含むポリイミド溶液(不揮発分30質量%)を得た。また、ポリイミド樹脂2の重量平均分子量は、25,000であった。
環流冷却器を連結した水分定量受器、窒素導入管、及び攪拌器を備えた、500mLのセパラブルフラスコを用意した。このフラスコに、4,4’-オキシジフタル酸無水物(ODPA)20.3g、γ-ブチロラクトン200g、トルエン20g、及び、5-(4-アミノフェノキシ)-3-[4-(4-アミノフェノキシ)フェニル]-1,1,3-トリメチルインダン29.6gを加えて、窒素気流下で45℃にて2時間攪拌して、反応を行った。次いで、この反応溶液を昇温し、約160℃に保持しながら、窒素気流下で縮合水をトルエンとともに共沸除去した。水分定量受器に所定量の水がたまっていること、及び、水の流出が見られなくなっていることを確認した。確認後、反応溶液を更に昇温し、200℃で1時間攪拌した。その後、冷却して、1,1,3-トリメチルインダン骨格を有するポリイミド樹脂3を含むポリイミド溶液(不揮発分20質量%)を得た。得られたポリイミド樹脂3は、下記式(X1)で表される繰り返し単位及び下記式(X2)で示す繰り返し単位を有していた。また、前記のポリイミド樹脂3の重量平均分子量は、12,000であった。
ビキシレノール型エポキシ樹脂(三菱化学社製「YX4000HK」、エポキシ当量約185)5部、ナフタレン型エポキシ樹脂(新日鉄住金化学社製「ESN475V」、エポキシ当量約332)5部、ビスフェノールAF型エポキシ樹脂(三菱化学社製「YL7760」、エポキシ当量約238)10部、シクロヘキサン型エポキシ樹脂(三菱化学社製「ZX1658GS」、エポキシ当量約135)2部、合成例1で得たポリイミド溶液(不揮発成分20質量%)100部、及びシクロヘキサノン10部の混合溶剤に撹拌しながら加熱溶解させた。室温にまで冷却した後、そこへ、ビフェニル骨格含有マレイミド樹脂(日本化薬社製「MIR-3000」、不揮発分70質量%のトルエン:MEKの1:1溶液)7.1部、トリアジン骨格含有クレゾールノボラック系硬化剤(DIC社製「LA3018-50P」、水酸基当量約151、固形分50%の2-メトキシプロパノール溶液)4部、活性エステル系硬化剤(DIC社製「EXB-8000L-65M」、活性基当量約220、不揮発成分65質量%のMEK溶液)6部、球形シリカ(アドマテックス社製「SC2500SQ」、平均粒径0.5μm、比表面積11.2m2/g、シリカ100部に対してN-フェニル-3-アミノプロピルトリメトキシシラン(信越化学工業社製、KBM573)1部で表面処理したもの)50部、アミン系硬化促進剤(4-ジメチルアミノピリジン(DMAP))0.2部を混合し、高速回転ミキサーで均一に分散した後に、カートリッジフィルター(ROKITECHNO社製「SHP020」)で濾過して、樹脂組成物1を調製した。
ビフェニル骨格含有マレイミド樹脂(日本化薬社製「MIR-3000」、不揮発分70質量%のトルエン:MEKの1:1溶液)7.1部を使用する代わりに、ポリフェニルメタンマレイミド樹脂(大和化成工業社製「BMI-2300」、不揮発分40質量%のMEK溶液)12.5部を使用したこと以外は、実施例1と同じ操作を行って、樹脂組成物2を調製した。
ビフェニル骨格含有マレイミド樹脂(日本化薬社製「MIR-3000」、不揮発分70質量%のトルエン:MEKの1:1溶液)の使用量を7.1部から14.2部に変更したこと、合成例1で得たポリイミド溶液(不揮発成分20質量%)100部を使用する代わりに、合成例2で得たポリイミド溶液(不揮発成分30質量%)66.7部を使用したこと以外は、実施例1と同じ操作を行って、樹脂組成物3を調製した。
合成例1で得たポリイミド溶液(不揮発成分20質量%)100部を使用する代わりに、合成例3で得たポリイミド溶液(不揮発成分20質量%)100部を使用したこと以外、実施例1と同じ操作を行って、樹脂組成物4を調製した。
ビフェニル骨格含有マレイミド樹脂(日本化薬社製「MIR-3000」、不揮発分70質量%のトルエン:MEKの1:1溶液)7.1部を使用しなかったこと以外は、実施例1と同じ操作を行って、樹脂組成物5を調製した。
ビフェニル骨格含有マレイミド樹脂(日本化薬社製「MIR-3000」、不揮発分70質量%のトルエン:MEKの1:1溶液)7.1部を使用する代わりに、ジフェニルメタンビスマレイミド樹脂(大和化成工業社製「BMI1000」、不揮発分40質量%のMEK溶液)12.5部を使用したこと以外は、実施例1と同じ操作を行って、樹脂組成物6を調製した。
合成例1で得たポリイミド溶液(不揮発成分20質量%)を使用しなかったこと、及びフェノキシ樹脂(三菱ケミカル社製「YX7553BH30」、固形分30質量%)66.7部使用したこと以外は、実施例1と同じ操作を行って、樹脂組成物7を調製した。
無機充填材100mg、及びメチルエチルケトン10gをバイアル瓶に秤取り、超音波にて10分間分散した。レーザー回折式粒径分布測定装置(堀場製作所社製「LA-960」)を使用して、使用光源波長を青色および赤色とし、フローセル方式で無機充填材の粒径分布を体積基準で測定した。得られた粒径分布から、メディアン径として、無機充填材の平均粒径を算出した。
BET全自動比表面積測定装置(マウンテック社製Macsorb HM-1210)を使用して、試料表面に窒素ガスを吸着させ、BET多点法を用いて比表面積を算出することで無機充填材の比表面積を測定した。
各実施例及び比較例の樹脂組成物をアルキド系離型剤で処理されたPETフィルム(厚さ38μm)の離型処理面上に、乾燥後の樹脂組成物層の厚さが50μmになるよう、ダイコータにて均一に塗布し、80~120℃(平均100℃)で6分間乾燥させて、樹脂シート1を得た。
各実施例及び比較例の樹脂組成物をアルキド系離型剤で処理されたPETフィルム(厚さ38μm)の離型処理面上に、乾燥後の樹脂組成物層の厚さが40μmになるよう、ダイコータにて均一に塗布し、80~120℃(平均100℃)で6分間乾燥させて、樹脂シート2を得た。
Claims (12)
- (B)成分の含有量が、樹脂組成物中の不揮発成分を100質量%としたとき、1質量%~40質量%である、請求項1に記載の樹脂組成物。
- (B)成分に対する式(B1)で表される化合物の質量割合が、樹脂組成物中の(B)成分を100質量%としたとき、10質量%以上である、請求項1に記載の樹脂組成物。
- さらに(D)無機充填材を含み又は含まず、(D)成分の含有量が、樹脂組成物中の不揮発成分を100質量%としたとき、70質量%以下である、請求項1に記載の樹脂組成物。
- さらに(D)無機充填材を含む、請求項1に記載の樹脂組成物。
- 25℃から150℃におけるZ方向の線熱膨張係数が、100ppm以下である、請求項1に記載の樹脂組成物。
- 多層フレキシブル基板の絶縁層形成用である、請求項1に記載の樹脂組成物。
- 請求項1~8の何れか1項に記載の樹脂組成物の硬化物。
- 支持体と、当該支持体上に設けられた請求項1~8の何れか1項に記載の樹脂組成物で形成された樹脂組成物層とを含む、樹脂シート。
- 請求項1~8の何れか1項に記載の樹脂組成物を硬化して形成される絶縁層を含む多層フレキシブル基板。
- 請求項11に記載の多層フレキシブル基板を備える、半導体装置。
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2018053092A (ja) * | 2016-09-28 | 2018-04-05 | 味の素株式会社 | 樹脂組成物 |
WO2019073891A1 (ja) * | 2017-10-10 | 2019-04-18 | 三井金属鉱業株式会社 | プリント配線板用樹脂組成物、樹脂付銅箔、銅張積層板、及びプリント配線板 |
WO2019188087A1 (ja) * | 2018-03-30 | 2019-10-03 | 三井金属鉱業株式会社 | 銅張積層板 |
WO2020045408A1 (ja) * | 2018-08-27 | 2020-03-05 | 積水化学工業株式会社 | 樹脂材料、積層構造体及び多層プリント配線板 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0339311A (ja) * | 1989-06-29 | 1991-02-20 | Shell Internatl Res Maatschappij Bv | マレイミド組成物 |
JP2962784B2 (ja) * | 1990-08-01 | 1999-10-12 | 東邦レーヨン株式会社 | ポリイミド硬化樹脂複合体及びその製法 |
JPH05339344A (ja) * | 1992-06-15 | 1993-12-21 | Hitachi Chem Co Ltd | 熱硬化性樹脂組成物、接着剤シート、接着剤付きポリイミドフィルム及び金属はく張りポリイミドフィルム |
JP3486934B2 (ja) * | 1993-01-06 | 2004-01-13 | 日立化成工業株式会社 | 熱硬化性樹脂組成物 |
JPH06345964A (ja) * | 1993-06-11 | 1994-12-20 | Hitachi Chem Co Ltd | 耐熱性熱硬化性樹脂組成物、接着剤シート、接着剤付きポリイミドフィルム及び金属はく張りポリイミドフィルム |
US20120059119A1 (en) * | 2009-05-08 | 2012-03-08 | Mitsubishi Gas Chemical Company, Inc. | Thermosetting polyimide resin composition, cured product, and adhesive |
WO2011010672A1 (ja) * | 2009-07-24 | 2011-01-27 | 住友ベークライト株式会社 | 樹脂組成物、樹脂シート、プリプレグ、金属張積層板、プリント配線板及び半導体装置 |
TWI519602B (zh) * | 2014-06-06 | 2016-02-01 | Elite Material Co Ltd | Low dielectric resin composition and the application of its resin film, semi-cured film and circuit board |
JP6635403B2 (ja) * | 2014-12-26 | 2020-01-22 | 荒川化学工業株式会社 | 樹脂付銅箔、銅張積層板、プリント配線板及び多層配線板 |
US11286346B2 (en) * | 2015-01-13 | 2022-03-29 | Showa Denko Materials Co., Ltd. | Resin composition, support with resin layer, prepreg, laminate, multilayered printed wiring board, and printed wiring board for millimeter-wave radar |
JP2016196557A (ja) * | 2015-04-03 | 2016-11-24 | 住友ベークライト株式会社 | プリント配線基板用樹脂組成物、プリプレグ、樹脂基板、金属張積層板、プリント配線基板、および半導体装置 |
TWI589628B (zh) * | 2015-12-09 | 2017-07-01 | 中山台光電子材料有限公司 | 樹脂組合物 |
JP7114214B2 (ja) * | 2016-05-24 | 2022-08-08 | 味の素株式会社 | 接着フィルム |
JP6766507B2 (ja) * | 2016-08-02 | 2020-10-14 | 味の素株式会社 | 樹脂組成物 |
WO2018062405A1 (ja) * | 2016-09-29 | 2018-04-05 | 積水化学工業株式会社 | 硬化体及び多層基板 |
US11098195B2 (en) * | 2017-02-07 | 2021-08-24 | Mitsubishi Gas Chemical Company, Inc. | Resin composition, prepreg, metal foil-clad laminate, resin sheet, and printed circuit board |
JP6866858B2 (ja) * | 2017-03-10 | 2021-04-28 | 味の素株式会社 | 樹脂組成物層 |
CN108727942A (zh) * | 2017-04-24 | 2018-11-02 | 味之素株式会社 | 树脂组合物 |
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2018053092A (ja) * | 2016-09-28 | 2018-04-05 | 味の素株式会社 | 樹脂組成物 |
WO2019073891A1 (ja) * | 2017-10-10 | 2019-04-18 | 三井金属鉱業株式会社 | プリント配線板用樹脂組成物、樹脂付銅箔、銅張積層板、及びプリント配線板 |
WO2019188087A1 (ja) * | 2018-03-30 | 2019-10-03 | 三井金属鉱業株式会社 | 銅張積層板 |
WO2020045408A1 (ja) * | 2018-08-27 | 2020-03-05 | 積水化学工業株式会社 | 樹脂材料、積層構造体及び多層プリント配線板 |
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