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JP5935462B2 - Photosensitive element, resist pattern forming method, printed wiring board manufacturing method - Google Patents

Photosensitive element, resist pattern forming method, printed wiring board manufacturing method Download PDF

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Publication number
JP5935462B2
JP5935462B2 JP2012085699A JP2012085699A JP5935462B2 JP 5935462 B2 JP5935462 B2 JP 5935462B2 JP 2012085699 A JP2012085699 A JP 2012085699A JP 2012085699 A JP2012085699 A JP 2012085699A JP 5935462 B2 JP5935462 B2 JP 5935462B2
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resin composition
photosensitive resin
meth
mass
resist pattern
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JP2012252320A (en
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雄大 深谷
雄大 深谷
宮坂 昌宏
昌宏 宮坂
純一 磯
純一 磯
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Resonac Corp
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Hitachi Chemical Co Ltd
Showa Denko Materials Co Ltd
Resonac Corp
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/027Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34
    • H01L21/0271Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers
    • H01L21/0273Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers characterised by the treatment of photoresist layers
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/002Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor using materials containing microcapsules; Preparing or processing such materials, e.g. by pressure; Devices or apparatus specially designed therefor
    • G03F7/0022Devices or apparatus
    • G03F7/003Devices or apparatus characterised by storage means for the light sensitive material, e.g. cartridges
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/0035Multiple processes, e.g. applying a further resist layer on an already in a previously step, processed pattern or textured surface
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/016Diazonium salts or compounds
    • G03F7/021Macromolecular diazonium compounds; Macromolecular additives, e.g. binders
    • G03F7/0212Macromolecular diazonium compounds; Macromolecular additives, e.g. binders characterised by the polymeric binder or the macromolecular additives other than the diazo resins or the polymeric diazonium compounds
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/027Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/0275Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with dithiol or polysulfide compounds
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00Apparatus or processes for manufacturing printed circuits
    • H05K3/10Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern
    • H05K3/18Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material
    • H05K3/181Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material by electroless plating
    • H05K3/182Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material by electroless plating characterised by the patterning method
    • H05K3/184Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material by electroless plating characterised by the patterning method using masks

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Manufacturing & Machinery (AREA)
  • Computer Hardware Design (AREA)
  • Power Engineering (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • Materials For Photolithography (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Manufacturing Of Printed Circuit Boards (AREA)
  • Manufacturing Of Printed Wiring (AREA)
  • Polymerisation Methods In General (AREA)

Description

本発明は、感光性樹脂組成物、並びにこれを用いた感光性エレメント、レジストパターンの形成方法及びプリント配線板の製造方法に関する。   The present invention relates to a photosensitive resin composition, a photosensitive element using the same, a method for forming a resist pattern, and a method for producing a printed wiring board.

近年、半導体素子の軽薄短小化、少量多品種化の傾向が進むにつれ、ICチップを基板上に搭載するために用いられるBGA(Ball Grid Array)等の半導体パッケージも多ピン化、狭小化が進み、これらを搭載するプリント配線板も高密度化が要求されている。   In recent years, semiconductor packages such as BGA (Ball Grid Array) used for mounting an IC chip on a substrate are becoming more and more pinned and narrowed as the trend toward lighter, thinner and smaller semiconductor devices is increasing. The printed wiring board on which these are mounted is also required to have a high density.

従来、プリント配線板の製造分野においては、エッチングやめっき等に用いられるレジスト材料として、支持フィルムと、該支持フィルム上に積層された感光性樹脂組成物からなる感光性樹脂組成物層と、これを被覆する保護フィルムとからなる感光性エレメントが広く用いられている。   Conventionally, in the field of production of printed wiring boards, as a resist material used for etching, plating, etc., a support film, a photosensitive resin composition layer composed of a photosensitive resin composition laminated on the support film, and this A photosensitive element comprising a protective film for covering the film is widely used.

プリント配線板は、感光性エレメントを用いて以下に示す方法で製造される。まず、感光性エレメントの保護フィルムを剥離しながら、感光性樹脂組成物層を基板上に積層(ラミネート)する。次に、感光性樹脂組成物層の所定部分に活性光線を照射して露光部を硬化させる。支持フィルムを剥離除去した後、未露光部を基板上から除去(現像)することにより、基板上に、感光性樹脂組成物の硬化物からなるレジストパターンが形成される。レジストパターンを形成した基板に対し、エッチング処理又はめっき処理を施して基板上に回路を形成した後、最終的にレジストを剥離除去することでプリント配線板が製造される。   A printed wiring board is manufactured by the method shown below using a photosensitive element. First, the photosensitive resin composition layer is laminated (laminated) on the substrate while peeling off the protective film of the photosensitive element. Next, a predetermined part of the photosensitive resin composition layer is irradiated with actinic rays to cure the exposed part. After the support film is peeled and removed, the unexposed portion is removed (developed) from the substrate, whereby a resist pattern made of a cured product of the photosensitive resin composition is formed on the substrate. A printed wiring board is manufactured by subjecting the substrate on which the resist pattern is formed to an etching process or a plating process to form a circuit on the substrate, and finally removing and removing the resist.

特に半導体パッケージ搭載基板の製造においては、レジストパターン形成後、めっき処理、レジスト剥離、ソフトエッチングを行うセミアディティブ工法(SAP)が主流になっている。   In particular, in manufacturing a semiconductor package mounting substrate, a semi-additive method (SAP) in which plating processing, resist peeling, and soft etching are performed after forming a resist pattern has become mainstream.

上記セミアディティブ工法(SAP)に用いられる感光性樹脂組成物には、従来の感光性樹脂組成物よりも微細配線が形成可能であることが要求される。   The photosensitive resin composition used for the semi-additive construction method (SAP) is required to be capable of forming finer wiring than the conventional photosensitive resin composition.

従来、微細配線が形成可能(解像度や密着性に優れる)な感光性樹脂組成物が多数提案されている(例えば、特許文献1〜3参照)。   Conventionally, a large number of photosensitive resin compositions capable of forming fine wiring (excellent in resolution and adhesion) have been proposed (see, for example, Patent Documents 1 to 3).

特開2005−301101号公報JP-A-2005-301101 特開2006−234995号公報JP 2006-234959 A 特開2006−154740号公報JP 2006-154740 A

しかしながら、上記特許文献1又は2に記載の感光性樹脂組成物を使用した場合でも、近年要求される解像度については改善の余地がある。また、本発明者らの検討により、上記特許文献3に記載の感光性樹脂組成物を使用すると、レジストパターンを形成する際のめっき工程において、レジストの端部でのめっき液への耐性(以下、「めっき耐性」という。)が低くなり、めっきもぐりが生じる点で改善の余地があることが判明した。   However, even when the photosensitive resin composition described in Patent Document 1 or 2 is used, there is room for improvement in the resolution required in recent years. In addition, when the photosensitive resin composition described in Patent Document 3 is used by the study of the present inventors, in the plating step when forming the resist pattern, the resistance to the plating solution at the end of the resist (hereinafter referred to as the resist pattern) It was found that there was room for improvement in that the plating resistance was reduced and the plating was peeled off.

めっき耐性を向上する手法としては、レジストに疎水性化合物を付与する手法や、ガラス転移温度を向上させる手法が一般的である。しかしながら、これらの手法では、疎水性向上により現像スカムの発生や、レジストの剥離残渣付着が生じたり、ガラス転移温度の向上によりレジスト柔軟性が低下し、めっきもぐりが改善されなかったりする問題があることを本発明者らは見出した。   As a technique for improving the plating resistance, a technique for imparting a hydrophobic compound to the resist and a technique for improving the glass transition temperature are generally used. However, in these methods, there is a problem that development scum is generated due to hydrophobicity improvement, resist peeling residue adherence occurs, resist flexibility is lowered due to an increase in glass transition temperature, and plating removal is not improved. The present inventors have found that.

また、レジストに親水性化合物を付与することで、レジスト柔軟性を向上させる手法を本発明者らは試みたが、レジストの密着性及びめっき耐性の低下がみられ、SAPに要求される微細配線形成を形成可能であり、且つめっき耐性に優れた感光性樹脂組成物を製造することは困難であった。   In addition, the present inventors tried a technique for improving resist flexibility by imparting a hydrophilic compound to the resist. However, the adhesion of the resist and the plating resistance are reduced, and fine wiring required for SAP It was difficult to produce a photosensitive resin composition that can be formed and has excellent plating resistance.

本発明は上記問題点に鑑みてなされたものであり、解像度及び密着性に優れ、且つめっき耐性が良好である感光性樹脂組成物、並びにこれを用いた感光性エレメント、レジストパターンの製造方法及びプリント配線板の製造方法を提供することを目的とする。   The present invention has been made in view of the above problems, a photosensitive resin composition having excellent resolution and adhesion, and good plating resistance, a photosensitive element using the same, a method for producing a resist pattern, and It aims at providing the manufacturing method of a printed wiring board.

本発明の第一の態様は、(A)バインダーポリマー、(B)エチレン性不飽和結合を有する光重合性化合物、及び(C)光重合開始剤を含有する感光性樹脂組成物であって、(A)成分が、(a1)ベンジル(メタ)アクリレート誘導体由来の構成単位を50〜80質量%、(a2)スチレン誘導体由来の構成単位を5〜40質量%、(a3)(メタ)アクリル酸アルキルエステル由来の構成単位を1〜20質量%、及び(a4)(メタ)アクリル酸由来の構成単位を5〜30質量%含む、感光性樹脂組成物である。   A first aspect of the present invention is a photosensitive resin composition comprising (A) a binder polymer, (B) a photopolymerizable compound having an ethylenically unsaturated bond, and (C) a photopolymerization initiator, (A) component is (a1) 50-80 mass% of structural units derived from benzyl (meth) acrylate derivative, (a2) 5-40 mass% of structural units derived from styrene derivative, (a3) (meth) acrylic acid It is a photosensitive resin composition containing 1 to 20% by mass of a structural unit derived from an alkyl ester and 5 to 30% by mass of a structural unit derived from (a4) (meth) acrylic acid.

かかる感光性樹脂組成物によれば、解像度及び密着性に優れ、且つめっき耐性が良好である。これは、バインダーポリマーが、特定の共重合成分を特定量含有することで、親水性と疎水性のバランスに優れるレジストを提供できたためであると、本発明者らは推察している。   According to such a photosensitive resin composition, the resolution and adhesion are excellent, and the plating resistance is good. The present inventors speculate that this is because the binder polymer contains a specific amount of a specific copolymerization component, thereby providing a resist having an excellent balance between hydrophilicity and hydrophobicity.

本発明の第二の態様は、支持フィルムと、該支持フィルム上に形成される上記光性樹脂組成物からなる感光性樹脂組成物層とを備える感光性エレメントである。   2nd aspect of this invention is a photosensitive element provided with a support film and the photosensitive resin composition layer which consists of the said photosensitive resin composition formed on this support film.

本発明の第三の態様は、上記感光性樹脂組成物からなる感光性樹脂組成物層を基板上に積層する積層工程と、上記感光性樹脂組成物層に光硬化部を形成させる露光工程と、上記光硬化部以外の上記感光性樹脂組成物層を除去する現像工程と、を含む、レジストパターンの形成方法である。本態様は、感光性樹脂組成物層を、感光性エレメントを用いて積層する態様でもよい。   The third aspect of the present invention is a lamination step of laminating a photosensitive resin composition layer comprising the photosensitive resin composition on a substrate, and an exposure step of forming a photocured portion on the photosensitive resin composition layer. And a developing step for removing the photosensitive resin composition layer other than the photocured portion. This aspect may be an aspect in which the photosensitive resin composition layer is laminated using a photosensitive element.

本発明の第四の態様は、上記レジストパターンの形成方法によりレジストパターンが形成される基板に対し、エッチング処理又はめっき処理を施す、プリント配線板の製造方法である。   According to a fourth aspect of the present invention, there is provided a printed wiring board manufacturing method in which an etching process or a plating process is performed on a substrate on which a resist pattern is formed by the resist pattern forming method.

本発明によれば解像度及び密着性に優れ、且つ薄板基材上においてもめっき耐性に優れる感光性樹脂組成物、並びにこれを用いた感光性エレメント、レジストパターンの製造方法及びプリント配線板の製造方法を提供することができる。   INDUSTRIAL APPLICABILITY According to the present invention, a photosensitive resin composition having excellent resolution and adhesion and excellent plating resistance even on a thin plate substrate, a photosensitive element using the same, a method for producing a resist pattern, and a method for producing a printed wiring board Can be provided.

本発明の感光性エレメントの一実施形態を示す模式断面図である。It is a schematic cross section which shows one Embodiment of the photosensitive element of this invention.

以下、本発明の一実施形態について説明するが、本発明はこれに限定されるものではない。なお、本発明における(メタ)アクリル酸とはアクリル酸及びメタクリル酸を意味し、(メタ)アクリレートとはアクリレート及びそれに対応するメタクリレートを意味し、(メタ)アクリロイル基とはアクリロイル基及びメタクリロイル基を意味する。   Hereinafter, although one embodiment of the present invention is described, the present invention is not limited to this. In the present invention, (meth) acrylic acid means acrylic acid and methacrylic acid, (meth) acrylate means acrylate and the corresponding methacrylate, and (meth) acryloyl group means acryloyl group and methacryloyl group. means.

(感光性樹脂組成物)
本実施形態の感光性樹脂組成物は、(A)バインダーポリマー(以下、「(A)成分」ともいう。)、(B)エチレン性不飽和結合を有する光重合性化合物(以下、「(B)成分」ともいう。)、及び(C)光重合開始剤(以下、「(C)成分」ともいう。)を含有する。以下、(A)〜(C)成分につき、詳細に説明する。
(Photosensitive resin composition)
The photosensitive resin composition of the present embodiment includes (A) a binder polymer (hereinafter also referred to as “(A) component”), (B) a photopolymerizable compound having an ethylenically unsaturated bond (hereinafter referred to as “(B ) Component ”) and (C) a photopolymerization initiator (hereinafter also referred to as“ component (C) ”). Hereinafter, the components (A) to (C) will be described in detail.

まず、(A)バインダーポリマーについて説明する。上記(A)バインダーポリマーは、後述の感光性エレメントにおいてフィルム形状を付与するための基材として機能する。   First, (A) the binder polymer will be described. The (A) binder polymer functions as a base material for imparting a film shape to the photosensitive element described later.

かかる(A)バインダーポリマーは、(a1)ベンジル(メタ)アクリレート誘導体由来の構成単位、(a2)スチレン誘導体由来の構成単位、(a3)(メタ)アクリル酸アルキルエステル由来の構成単位、及び(a4)(メタ)アクリル酸由来の構成単位を含む。これらの構成単位を含むバインダーポリマーは、それぞれの構成単位に対応する単量体、すなわちベンジル(メタ)アクリレート誘導体、スチレン誘導体、(メタ)アクリル酸アルキルエステル、及び(メタ)アクリル酸を含有する単量体組成物を共重合させることにより得られる。このようにして得られる共重合体において各構成単位は、いわゆるランダム共重合体のように共重合体中にランダムに含まれていてもよく、或いはブロック共重合体のように一部の特定の構成単位が局在して存在する共重合体であってもよい。そして、上記構成単位のそれぞれは単一種であっても複数種であってもよい。   The (A) binder polymer comprises (a1) a structural unit derived from a benzyl (meth) acrylate derivative, (a2) a structural unit derived from a styrene derivative, (a3) a structural unit derived from a (meth) acrylic acid alkyl ester, and (a4 ) Containing structural units derived from (meth) acrylic acid. The binder polymer containing these structural units is a monomer containing a monomer corresponding to each structural unit, that is, a benzyl (meth) acrylate derivative, a styrene derivative, a (meth) acrylic acid alkyl ester, and a (meth) acrylic acid. It is obtained by copolymerizing the monomer composition. In the copolymer thus obtained, each structural unit may be randomly contained in the copolymer such as a so-called random copolymer, or some specific unit such as a block copolymer. It may be a copolymer in which structural units exist in a localized manner. And each of the said structural unit may be single type, or multiple types.

(A)バインダーポリマーは、(a1)ベンジル(メタ)アクリレート誘導体由来の構成単位を特定量含むことにより、樹脂の柔軟性を維持しながら密着性に優れる。ベンジル(メタ)アクリレート誘導体の具体例としては、例えばベンジル(メタ)アクリレート、4−メチルベンジル(メタ)アクリレート、4−エチルベンジル(メタ)アクリレート、4−tertブチルベンジル(メタ)アクリレート、4−メトキシベンジル(メタ)アクリレート、4−エトキシベンジル(メタ)アクリレート、4−ヒドロキシルベンジル(メタ)アクリレート、4−クロロベンジル(メタ)アクリレートが挙げられる。   (A) A binder polymer is excellent in adhesiveness, maintaining the softness | flexibility of resin by including the specific amount of the structural unit derived from (a1) benzyl (meth) acrylate derivative. Specific examples of the benzyl (meth) acrylate derivative include, for example, benzyl (meth) acrylate, 4-methylbenzyl (meth) acrylate, 4-ethylbenzyl (meth) acrylate, 4-tertbutylbenzyl (meth) acrylate, 4-methoxy Examples include benzyl (meth) acrylate, 4-ethoxybenzyl (meth) acrylate, 4-hydroxylbenzyl (meth) acrylate, and 4-chlorobenzyl (meth) acrylate.

(A)バインダーポリマーは、(a2)スチレン誘導体由来の構成単位を特定量含むことにより、細線部の密着性、解像度に優れる。スチレン誘導体の具体例としては、例えばスチレン、ビニルトルエン、p−メチルスチレン、p−クロロスチレンが挙げられる。   (A) A binder polymer is excellent in the adhesiveness and resolution of a thin wire | line part by including the specific amount of the structural unit derived from (a2) styrene derivative. Specific examples of the styrene derivative include styrene, vinyltoluene, p-methylstyrene, and p-chlorostyrene.

(A)バインダーポリマーは、(a3)(メタ)アクリル酸アルキルエステル由来の構成単位を特定量含むことにより、バインダーポリマーの柔軟性と強靭性の両立に優れる。
(メタ)アクリル酸アルキルエステルにおけるアルキル基は、直鎖状又は分岐状の炭素数1〜12のアルキル基であると好ましく、直鎖状又は分岐状の炭素数1〜8のアルキル基であるとより好ましく、直鎖状の炭素数1〜4のアルキル基であるとさらに好ましく、メチル基であると特に好ましい。
(A) The binder polymer is excellent in both flexibility and toughness of the binder polymer by including a specific amount of the structural unit derived from (a3) (meth) acrylic acid alkyl ester.
The alkyl group in the (meth) acrylic acid alkyl ester is preferably a linear or branched alkyl group having 1 to 12 carbon atoms, and is a linear or branched alkyl group having 1 to 8 carbon atoms. More preferably, it is a linear alkyl group having 1 to 4 carbon atoms, more preferably a methyl group.

上記(メタ)アクリル酸アルキルエステルの具体例としては、例えば(メタ)アクリル酸メチル、(メタ)アクリル酸エチル、(メタ)アクリル酸プロピル、(メタ)アクリル酸イソプロピル、(メタ)アクリル酸ブチル、(メタ)アクリル酸tert−ブチル、(メタ)アクリル酸ペンチル、(メタ)アクリル酸ヘキシル、(メタ)アクリル酸ヘプチル、(メタ)アクリル酸オクチル、(メタ)アクリル酸2−エチルヘキシルが挙げられる。   Specific examples of the (meth) acrylic acid alkyl ester include, for example, methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, isopropyl (meth) acrylate, butyl (meth) acrylate, Examples include tert-butyl (meth) acrylate, pentyl (meth) acrylate, hexyl (meth) acrylate, heptyl (meth) acrylate, octyl (meth) acrylate, and 2-ethylhexyl (meth) acrylate.

(A)バインダーポリマーは、(a4)(メタ)アクリル酸由来の構成単位を特定量含むことにより、アルカリ現像性に優れる。   (A) The binder polymer is excellent in alkali developability by containing a specific amount of a structural unit derived from (a4) (meth) acrylic acid.

なお、(A)バインダーポリマーは、上記(a1)〜(a4)以外の構成単位を含んでいてもよい。   The (A) binder polymer may contain structural units other than the above (a1) to (a4).

(A)バインダーポリマーは、(a1)ベンジル(メタ)アクリレート誘導体由来の構成単位を50〜80質量%含み、樹脂の柔軟性を維持しながら密着性により優れる点では、50〜75質量%含むことが好ましく、50〜70質量%含むことがより好ましく、50〜65質量%含むことがさらに好ましい。   (A) The binder polymer contains 50 to 80% by mass of the structural unit derived from (a1) benzyl (meth) acrylate derivative, and 50 to 75% by mass in terms of better adhesion while maintaining the flexibility of the resin. Is preferable, it is more preferable to contain 50-70 mass%, and it is more preferable to include 50-65 mass%.

(A)バインダーポリマーは、(a2)スチレン誘導体由来の構成単位を5〜40質量%含み、密着性及び解像度にさらに優れる点では、5〜35質量%含むことが好ましい。また、(a3)(メタ)アクリル酸アルキルエステル由来の構成単位を1〜20質量%含むが、レジストに親水性と疎水性をさらにバランス良く供与する点では、1〜15質量%含むことが好ましく、1〜10質量%含むことがより好ましく、1〜5質量%含むことがさらに好ましい。さらに、(a4)(メタ)アクリル酸由来の構成単位を5〜30質量%含むが、アルカリ現像性にさらに優れる点では、5〜25質量%含むことが好ましく、10〜25質量%含むことがより好ましい。   (A) The binder polymer preferably contains 5 to 35% by mass of (a2) a structural unit derived from a styrene derivative and is further excellent in adhesion and resolution. In addition, (a3) the structural unit derived from (meth) acrylic acid alkyl ester is contained in an amount of 1 to 20% by mass, but it is preferably contained in an amount of 1 to 15% by mass in terms of providing the resist with a more balanced hydrophilicity and hydrophobicity. It is more preferable to contain 1-10 mass%, and it is still more preferable to contain 1-5 mass%. Furthermore, it contains 5 to 30% by mass of the structural unit derived from (a4) (meth) acrylic acid, but it is preferably 5 to 25% by mass and more preferably 10 to 25% by mass in terms of further excellent alkali developability. More preferred.

また、(A)バインダーポリマーの重量平均分子量(Mw)は20,000〜150,000であることが好ましく、30,000〜100,000であることがより好ましく、40,000〜80,000であることがさらに好ましく、40,000〜60,000であることが特に好ましい。テント信頼性にさらに優れる点では、Mwが20,000以上であることが好ましく、30,000以上であることがより好ましく、40,000以上であることがさらに好ましい。一方、現像性及び解像性にさらに優れる点では、150,000以下であることが好ましく、100,000以下であることがより好ましく、80,000以下であることがさらに好ましく、60,000以下であることが特に好ましい。なお、本発明においてMwは、ゲルパーミエーションクロマトグラフィー(GPC)による標準ポリスチレンの換算の重量平均分子量をいう。   The weight average molecular weight (Mw) of the (A) binder polymer is preferably 20,000 to 150,000, more preferably 30,000 to 100,000, and 40,000 to 80,000. More preferably, it is particularly preferably 40,000 to 60,000. In terms of further excellent tent reliability, Mw is preferably 20,000 or more, more preferably 30,000 or more, and further preferably 40,000 or more. On the other hand, in terms of further excellent developability and resolution, it is preferably 150,000 or less, more preferably 100,000 or less, further preferably 80,000 or less, and 60,000 or less. It is particularly preferred that In the present invention, Mw refers to a weight average molecular weight in terms of standard polystyrene by gel permeation chromatography (GPC).

また、(A)バインダーポリマーの酸価(mgKOH/g)は、13〜78であることが好ましく、39〜65であることがより好ましく、52〜62であることがさらに好ましい。なお、本明細書中で酸価は、溶液中のバインダーポリマー1gに対する水酸化カリウムのmg数を表し、測定方法は実施例に記載の方法と同一とする。   The acid value (mgKOH / g) of the (A) binder polymer is preferably 13 to 78, more preferably 39 to 65, and still more preferably 52 to 62. In addition, in this specification, an acid value represents the mg number of potassium hydroxide with respect to 1g of binder polymers in a solution, and the measuring method is made the same as the method as described in an Example.

なお、本実施形態の感光性樹脂組成物は、上記(a1)〜(a4)を所定量含有するバインダーポリマーの他に、従来公知のバインダーポリマーを併用して使用することができる。   In addition, the photosensitive resin composition of this embodiment can be used in combination with a conventionally known binder polymer in addition to the binder polymer containing a predetermined amount of the above (a1) to (a4).

(B)エチレン性不飽和結合を有する光重合性化合物は、光架橋が可能であれば特に制限なく使用できる。その具体例としては、ビスフェノールA系(メタ)アクリレート化合物、水添ビスフェノールA系(メタ)アクリレート化合物、ポリアルキレングリコール(メタ)アクリレート、ウレタンモノマー、ペンタエリスリトール(メタ)アクリレート、トリメチロールプロパン(メタ)アクリレートが挙げられる。これらは単独で又は2種以上を組み合わせて使用される。   (B) The photopolymerizable compound having an ethylenically unsaturated bond can be used without particular limitation as long as photocrosslinking is possible. Specific examples thereof include bisphenol A (meth) acrylate compounds, hydrogenated bisphenol A (meth) acrylate compounds, polyalkylene glycol (meth) acrylates, urethane monomers, pentaerythritol (meth) acrylates, and trimethylolpropane (meth). An acrylate is mentioned. These are used alone or in combination of two or more.

上記の中でも、解像度及びめっき耐性を向上させる観点から、ビスフェノールA系ジ(メタ)アクリレート化合物を含むことが好ましい。ビスフェノールA系ジ(メタ)アクリレート化合物としては、例えば、下記一般式(1)で表される化合物が挙げられる。   Among these, from the viewpoint of improving resolution and plating resistance, it is preferable to include a bisphenol A di (meth) acrylate compound. Examples of the bisphenol A-based di (meth) acrylate compound include compounds represented by the following general formula (1).

Figure 0005935462
Figure 0005935462

上記式(1)中、Rはそれぞれ独立に、水素原子又はメチル基を示す。EO、POはそれぞれ、オキシエチレン基、オキシプロピレン基を示す。m、m、n、nはそれぞれ0〜40を示し、m+m(平均値)は1〜40、n+nは0〜20である。なお、EO、POはどちらがフェノール性水酸基側にあっても良い。m、m、n及びnは構成単位の数を示す。従って単一の分子においては整数値を示し、複数種の分子の集合体としては平均値である有理数を示す。以下、構成単位の数については同様である。 In said formula (1), R shows a hydrogen atom or a methyl group each independently. EO and PO represent an oxyethylene group and an oxypropylene group, respectively. m 1 , m 2 , n 1 and n 2 each represent 0 to 40, m 1 + m 2 (average value) is 1 to 40, and n 1 + n 2 is 0 to 20. Either EO or PO may be on the phenolic hydroxyl group side. m 1 , m 2 , n 1 and n 2 represent the number of structural units. Therefore, an integer value is shown in a single molecule, and a rational number that is an average value is shown as an aggregate of a plurality of types of molecules. Hereinafter, the same applies to the number of structural units.

めっき耐性により優れる点では、上記一般式(1)で表される化合物中、(1−1)m+m(平均値)が5以下である化合物と、(1−2)m+m(平均値)が6〜40である化合物を組み合わせて使用することが好ましい。 From the viewpoint of excellent by plating resistance, in the compounds represented by the above general formula (1), the compound is (1-1) m 1 + m 2 (average value) is 5 or less, (1-2) m 1 + m 2 It is preferable to use a combination of compounds having an (average value) of 6 to 40.

(1−1)m+m(平均値)が5以下である化合物としては、例えばm+m(平均値)が4である新中村化学(株)製BPE−200を用いることができ、(1−2)m+m(平均値)が6〜40である化合物としては、例えばm+m(平均値)が10である新中村化学(株)製BPE−500を用いることができる。 (1-1) As a compound whose m 1 + m 2 (average value) is 5 or less, for example, BPE-200 manufactured by Shin-Nakamura Chemical Co., Ltd. whose m 1 + m 2 (average value) is 4 can be used. (1-2) As a compound whose m 1 + m 2 (average value) is 6 to 40, for example, BPE-500 manufactured by Shin-Nakamura Chemical Co., Ltd. whose m 1 + m 2 (average value) is 10 is used. Can do.

また、(B)エチレン性不飽和結合を有する光重合性化合物は、ビスフェノールA系ジ(メタ)アクリレート化合物に加えて、下記式(2)で表される化合物をさらに含むことが好ましい。   Moreover, it is preferable that the (B) photopolymerizable compound which has an ethylenically unsaturated bond further contains the compound represented by following formula (2) in addition to the bisphenol A di (meth) acrylate compound.

Figure 0005935462

上記式(2)中、R14及びR15はそれぞれ独立に水素原子又はメチル基を示し、EO及びPOは上記と同義であり、sは1〜30を示し、r及びrはそれぞれ0〜30を示し、r+r(平均値)は1〜30である。
Figure 0005935462

In the above formula (2), R 14 and R 15 each independently represent a hydrogen atom or a methyl group, EO and PO are as defined above, s 1 represents a 1 to 30, r 1 and r 2 are each It indicates 0~30, r 1 + r 2 (average value) is 1 to 30.

式(2)で表される化合物の具体例としては、R14及びR15がメチル基、r+r=4(平均値)、s=12(平均値)であるビニル化合物(日立化成工業社製、商品名:FA−023M)が挙げられる。 Specific examples of the compound represented by the formula (2) include vinyl compounds in which R 14 and R 15 are methyl groups, r 1 + r 2 = 4 (average value), and s 1 = 12 (average value) (Hitachi Chemical) (Trade name: FA-023M, manufactured by Kogyo Co., Ltd.).

(C)光重合開始剤は、特に制限なく使用できるが、その具体例としては、ベンゾフェノン、N,N’−テトラメチル−4,4’−ジアミノベンゾフェノン(ミヒラーケトン)、N,N’−テトラエチル−4,4’−ジアミノベンゾフェノン、4−メトキシ−4’−ジメチルアミノベンゾフェノン、2−ベンジル−2−ジメチルアミノ−1−(4−モルホリノフェニル)−ブタノン−1、2−メチル−1−[4−(メチルチオ)フェニル]−2−モルフォリノ−プロパノン−1等の芳香族ケトン;2−エチルアントラキノン、フェナントレンキノン、2−tert−ブチルアントラキノン、オクタメチルアントラキノン、1,2−ベンズアントラキノン、2,3−ベンズアントラキノン、2−フェニルアントラキノン、2,3−ジフェニルアントラキノン、1−クロロアントラキノン、2−メチルアントラキノン、1,4−ナフトキノン、9,10−フェナンタラキノン、2−メチル1,4−ナフトキノン、2,3−ジメチルアントラキノン等のキノン類;ベンゾインメチルエーテル、ベンゾインエチルエーテル、ベンゾインフェニルエーテル等のベンゾインエーテル化合物、ベンゾイン、メチルベンゾイン、エチルベンゾイン等のベンゾイン化合物;ベンジルジメチルケタール等のベンジル誘導体、2−(o−クロロフェニル)−4,5−ジフェニルイミダゾール二量体、2−(o−クロロフェニル)−4,5−ジ(メトキシフェニル)イミダゾール二量体、2−(o−フルオロフェニル)−4,5−ジフェニルイミダゾール二量体、2−(o−メトキシフェニル)−4,5−ジフェニルイミダゾール二量体、2−(p−メトキシフェニル)−4,5−ジフェニルイミダゾール二量体等の2,4,5−トリアリールイミダゾール二量体;9−フェニルアクリジン、1,7−ビス(9,9’−アクリジニル)ヘプタン等のアクリジン誘導体、N−フェニルグリシン、N−フェニルグリシン誘導体、クマリン系化合物が挙げられる。これらは、単独で又は2種類以上を組み合わせて使用される。   (C) The photopolymerization initiator can be used without particular limitation. Specific examples thereof include benzophenone, N, N′-tetramethyl-4,4′-diaminobenzophenone (Michler ketone), N, N′-tetraethyl- 4,4′-diaminobenzophenone, 4-methoxy-4′-dimethylaminobenzophenone, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1,2-methyl-1- [4- Aromatic ketones such as (methylthio) phenyl] -2-morpholino-propanone-1; 2-ethylanthraquinone, phenanthrenequinone, 2-tert-butylanthraquinone, octamethylanthraquinone, 1,2-benzanthraquinone, 2,3-benz Anthraquinone, 2-phenylanthraquinone, 2,3-diphenyla Quinones such as traquinone, 1-chloroanthraquinone, 2-methylanthraquinone, 1,4-naphthoquinone, 9,10-phenantharaquinone, 2-methyl 1,4-naphthoquinone, 2,3-dimethylanthraquinone; benzoin methyl ether, Benzoin ether compounds such as benzoin ethyl ether and benzoin phenyl ether, benzoin compounds such as benzoin, methyl benzoin and ethyl benzoin; benzyl derivatives such as benzyldimethyl ketal, 2- (o-chlorophenyl) -4,5-diphenylimidazole dimer 2- (o-chlorophenyl) -4,5-di (methoxyphenyl) imidazole dimer, 2- (o-fluorophenyl) -4,5-diphenylimidazole dimer, 2- (o-methoxyphenyl) -4,5-di 2,4,5-triarylimidazole dimers such as phenylimidazole dimer, 2- (p-methoxyphenyl) -4,5-diphenylimidazole dimer; 9-phenylacridine, 1,7-bis ( Acridine derivatives such as 9,9′-acridinyl) heptane, N-phenylglycine, N-phenylglycine derivatives, and coumarin compounds. These are used alone or in combination of two or more.

上記の中でも、密着性及び感度の見地から、2,4,5−トリアリールイミダゾール二量体、より好ましくは2−(O−クロロフェニル)−4,5−ジフェニルイミダゾール二量体を含むことが好ましい。   Among the above, from the viewpoint of adhesion and sensitivity, 2,4,5-triarylimidazole dimer, more preferably 2- (O-chlorophenyl) -4,5-diphenylimidazole dimer is preferably included. .

感光性樹脂組成物における(A)バインダーポリマーの含有量は、(A)成分及び(B)成分の総量100質量部に対して、40〜80質量部であることが好ましく、45〜75質量部であることがより好ましく、50〜70質量部であることがさらに好ましい。感光性エレメントとして用いた場合に塗膜性にさらに優れる点では、40質量部以上であることが好ましく、45質量部以上であることがより好ましく、50質量部以上であることがさらに好ましい。また、光感度にさらに優れる点では、80質量部以下であることが好ましく、75質量部以下であることがより好ましく、70質量部以下であることがさらに好ましい。   The content of the (A) binder polymer in the photosensitive resin composition is preferably 40 to 80 parts by mass with respect to 100 parts by mass of the total amount of the components (A) and (B), and 45 to 75 parts by mass. It is more preferable that it is 50-70 mass parts. When used as a photosensitive element, it is preferably 40 parts by mass or more, more preferably 45 parts by mass or more, and still more preferably 50 parts by mass or more in terms of further excellent coating properties. Moreover, in the point which is further excellent in a photosensitivity, it is preferable that it is 80 mass parts or less, It is more preferable that it is 75 mass parts or less, It is further more preferable that it is 70 mass parts or less.

感光性樹脂組成物における(C)光重合開始剤の含有量は、光感度と内部硬化性に優れる点では、(A)成分及び(B)成分の総量100質量部に対して、0.01〜5質量部であることが好ましく、0.1〜4.5質量部であることがより好ましく、1〜4質量部であることがより好ましい。   The content of the photopolymerization initiator (C) in the photosensitive resin composition is 0.01 with respect to 100 parts by mass of the total amount of the component (A) and the component (B) in terms of excellent photosensitivity and internal curability. It is preferable that it is -5 mass parts, It is more preferable that it is 0.1-4.5 mass parts, It is more preferable that it is 1-4 mass parts.

感光性樹脂組成物には、必要に応じて、分子内に少なくとも1つのカチオン重合可能な環状エーテル基を有する光重合性化合物、カチオン重合開始剤、増感剤、マラカイトグリーン等の染料、トリブロモメチルフェニルスルホン、ロイコクリスタルバイオレット等の光発色剤、熱発色防止剤、p−トルエンスルホンアミド等の可塑剤、顔料、充填剤、消泡剤、難燃剤、安定剤、密着性付与剤、レベリング剤、剥離促進剤、酸化防止剤、香料、イメージング剤、熱架橋剤等の添加剤を添加してもよい。これらの添加剤を感光性樹脂組成物に添加した場合のその含有量は、(A)成分及び(B)成分の総量100質量部に対して各々0.01〜20質量部程度とすることができる。これらは単独で又は2種類以上を組み合わせて使用される。   If necessary, the photosensitive resin composition may include a photopolymerizable compound having at least one cationically polymerizable cyclic ether group in the molecule, a cationic polymerization initiator, a sensitizer, a dye such as malachite green, tribromo, and the like. Photochromic agents such as methylphenylsulfone and leucocrystal violet, thermochromic inhibitors, plasticizers such as p-toluenesulfonamide, pigments, fillers, antifoaming agents, flame retardants, stabilizers, adhesion promoters, leveling agents Additives such as a peeling accelerator, an antioxidant, a fragrance, an imaging agent, and a thermal crosslinking agent may be added. When these additives are added to the photosensitive resin composition, the content thereof is about 0.01 to 20 parts by mass with respect to 100 parts by mass of the total amount of the component (A) and the component (B). it can. These may be used alone or in combination of two or more.

感光性樹脂組成物における(A)、(B)及び(C)成分の合計の含有量は、感光性樹脂組成物の固形分全量に対して、90質量%以上であることが好ましく、95質量%以上であることがより好ましい。   The total content of the components (A), (B) and (C) in the photosensitive resin composition is preferably 90% by mass or more with respect to the total solid content of the photosensitive resin composition, and is 95% by mass. % Or more is more preferable.

感光性樹脂組成物は、必要に応じて、メタノール、エタノール、アセトン、メチルエチルケトン、メチルセロソルブ、エチルセロソルブ、トルエン、N,N−ジメチルホルムアミド、プロピレングリコールモノメチルエーテル等の有機溶剤又はこれらの混合溶剤に溶解させて固形分30〜60質量%程度の溶液として用いることができる。   The photosensitive resin composition is dissolved in an organic solvent such as methanol, ethanol, acetone, methyl ethyl ketone, methyl cellosolve, ethyl cellosolve, toluene, N, N-dimethylformamide, propylene glycol monomethyl ether or a mixed solvent thereof as necessary. And can be used as a solution having a solid content of about 30 to 60% by mass.

感光性樹脂組成物は、特に制限はないが、銅、銅系合金、鉄、鉄系合金等の金属面上に、液状レジストとして塗布して乾燥後、必要に応じて保護フィルムを被覆して用いるか、感光性エレメントの形態で用いられることが好ましい。   The photosensitive resin composition is not particularly limited, but is coated as a liquid resist on a metal surface such as copper, a copper-based alloy, iron, or an iron-based alloy, dried, and then covered with a protective film as necessary. It is preferably used in the form of a photosensitive element.

(感光性エレメント)
以下、図1に基づいて本実施形態の感光性エレメントについて説明する。本実施形態の感光性エレメント1は支持フィルム10と、上述の感光性樹脂組成物からなる感光性樹脂組成物層20とを備える。感光性樹脂組成物層20は支持フィルム10の第1の主面12上に設けられている。また、支持フィルム10は、第1の主面12とは反対側に第2の主面14を有している。また、感光性樹脂組成物層20の支持フィルム10とは反対側の面には保護フィルムが設けられていてもよい。なお、上記感光性樹脂組成物層は、上記感光性樹脂組成物が未硬化状態のものである。
(Photosensitive element)
Hereinafter, the photosensitive element of this embodiment is demonstrated based on FIG. The photosensitive element 1 of this embodiment includes a support film 10 and a photosensitive resin composition layer 20 made of the above-described photosensitive resin composition. The photosensitive resin composition layer 20 is provided on the first main surface 12 of the support film 10. The support film 10 has a second main surface 14 on the side opposite to the first main surface 12. Moreover, the protective film may be provided in the surface on the opposite side to the support film 10 of the photosensitive resin composition layer 20. As shown in FIG. The photosensitive resin composition layer is one in which the photosensitive resin composition is in an uncured state.

感光性樹脂組成物層20の厚みは、用途により異なるが、乾燥後の厚みで1〜100μm程度であることが好ましい。セミアディティブ工法(SAP)に用いる点では、5〜50μmであることが好ましく、5〜30μmであることがより好ましい。   Although the thickness of the photosensitive resin composition layer 20 changes with uses, it is preferable that it is about 1-100 micrometers by the thickness after drying. In terms of use in the semi-additive construction method (SAP), the thickness is preferably 5 to 50 μm, and more preferably 5 to 30 μm.

支持フィルム10は、例えばポリエチレンテレフタレート、ポリプロピレン、ポリエチレン、ポリエステル等の重合体フィルムからなるものを用いることができる。これらの重合体フィルムの厚みは、1〜100μmとすることが好ましい。   The support film 10 may be made of a polymer film such as polyethylene terephthalate, polypropylene, polyethylene, or polyester. The thickness of these polymer films is preferably 1 to 100 μm.

感光性樹脂組成物層20は、上述の感光性樹脂組成物を支持フィルム10上に塗布、乾燥することにより得ることができる。上記塗布は、例えば、ロールコータ、コンマコータ、グラビアコータ、エアーナイフコータ、ダイコータ、バーコータ等の公知の方法で行うことができる。また、乾燥は、70〜150℃、5〜30分間程度で行うことができる。   The photosensitive resin composition layer 20 can be obtained by applying and drying the above-described photosensitive resin composition on the support film 10. The application can be performed by a known method such as a roll coater, a comma coater, a gravure coater, an air knife coater, a die coater, or a bar coater. Moreover, drying can be performed at 70-150 degreeC and about 5 to 30 minutes.

また、感光性エレメント1は、感光性樹脂組成物層20、支持フィルム10、保護フィルムの他に、クッション層、接着層、光吸収層、ガスバリア層等の中間層や保護層を備えていてもよい。   Moreover, the photosensitive element 1 may be provided with intermediate | middle layers and protective layers, such as a cushion layer, an adhesive layer, a light absorption layer, and a gas barrier layer other than the photosensitive resin composition layer 20, the support film 10, and a protective film. Good.

感光性エレメント1は、例えば、そのまま又は上記保護フィルムをさらに積層した状態で円筒状の巻芯に巻きとって貯蔵される。なおこの際、支持フィルム10が外側になるように巻き取られることが好ましい。上記ロール状の感光性エレメントロールの端面には、端面保護の見地から端面セパレータを設置することが好ましく、耐エッジフュージョンの見地から防湿端面セパレータを設置することが好ましい。また、梱包方法として、透湿性の小さいブラックシートに包んで包装することが好ましい。   The photosensitive element 1 is stored, for example, by being wound around a cylindrical core as it is or in a state in which the protective film is further laminated. At this time, it is preferable that the support film 10 is wound up so as to be on the outside. An end face separator is preferably installed on the end face of the roll-shaped photosensitive element roll from the viewpoint of end face protection, and a moisture-proof end face separator is preferably installed from the viewpoint of edge fusion resistance. Moreover, as a packing method, it is preferable to wrap and package in a black sheet with low moisture permeability.

(レジストパターンの形成方法)
上記感光性エレメント1を用いてレジストパターンを形成する方法としては、例えば以下の方法が挙げられる。
(Method for forming resist pattern)
Examples of a method for forming a resist pattern using the photosensitive element 1 include the following methods.

保護フィルムが存在している場合には、保護フィルムを除去後、感光性樹脂組成物層20を70〜130℃程度に加熱しながら基板に0.1〜1MPa程度(1〜10kgf/cm程度)の圧力で圧着することにより、感光性樹脂組成物層を積層する。なお、減圧下で積層することも可能である。積層される表面は、通常金属面であるが、特に制限はない。 When the protective film is present, after removing the protective film, the substrate is heated to about 0.1 to 1 MPa (about 1 to 10 kgf / cm 2) while heating the photosensitive resin composition layer 20 to about 70 to 130 ° C. The photosensitive resin composition layer is laminated by pressure bonding at a pressure of). It is also possible to stack under reduced pressure. The surface to be laminated is usually a metal surface, but is not particularly limited.

このようにして積層が完了した感光性樹脂組成物層20は、ネガ又はポジマスクパターンを通して活性光線が画像状に照射される。上記活性光線の光源としては、公知の光源、例えば、カーボンアーク灯、水銀蒸気アーク灯、高圧水銀灯、キセノンランプ等の紫外線、可視光などを有効に放射するものが用いられる。   The photosensitive resin composition layer 20 thus laminated is irradiated with actinic rays in an image form through a negative or positive mask pattern. As the light source of the actinic light, a known light source, for example, a light source that effectively emits ultraviolet light, visible light, or the like such as a carbon arc lamp, a mercury vapor arc lamp, a high-pressure mercury lamp, or a xenon lamp is used.

露光方法としては、近年、DLP(Digital Light Processing)やLDI(Laser Direct Imaging)と呼ばれる、パターンのデジタルデータを直接感光性樹脂組成物層に描画する直接描画露光法が実用化されているが、本発明の感光性樹脂組成物は、直接描画露光法に好適に用いることができる。即ち、本発明の実施形態の感光性樹脂組成物は、直接描画露光方法に好適に使用することができる。即ち、本発明の好適な実施形態の一つは、(A)バインダーポリマー、(B)エチレン性不飽和結合を有する光重合性化合物、及び(C)光重合開始剤を含有する感光性樹脂組成物であって、上記(A)成分が、(a1)ベンジル(メタ)アクリレート誘導体由来の構成単位を50〜80質量%、(a2)スチレン誘導体由来の構成単位を5〜40質量%、(a3)(メタ)アクリル酸アルキルエステル由来の構成単位を1〜20質量%、及び(a4)(メタ)アクリル酸由来の構成単位を5〜30質量%含む、感光性樹脂組成物の直接描画露光法によりレジストパターンを形成するための応用である。   As an exposure method, in recent years, a direct drawing exposure method called DLP (Digital Light Processing) or LDI (Laser Direct Imaging), which directly draws digital data of a pattern on a photosensitive resin composition layer, has been put into practical use. The photosensitive resin composition of this invention can be used suitably for a direct drawing exposure method. That is, the photosensitive resin composition of the embodiment of the present invention can be suitably used for a direct drawing exposure method. That is, one preferred embodiment of the present invention is a photosensitive resin composition containing (A) a binder polymer, (B) a photopolymerizable compound having an ethylenically unsaturated bond, and (C) a photopolymerization initiator. The component (A) is 50 to 80% by mass of the structural unit derived from the (a1) benzyl (meth) acrylate derivative, (a2) 5 to 40% by mass of the structural unit derived from the styrene derivative, (a3 1) 20% by mass of a structural unit derived from (meth) acrylic acid alkyl ester, and 5-30% by mass of a structural unit derived from (a4) (meth) acrylic acid. This is an application for forming a resist pattern.

露光後、感光性樹脂組成物層上に支持フィルム10が存在している場合には、支持フィルム10を除去した後、アルカリ性水溶液、水系現像液、有機溶剤等の現像液によるウエット現像、ドライ現像等で未露光部を除去して現像し、レジストパターンを形成することができる。   After the exposure, when the support film 10 is present on the photosensitive resin composition layer, the support film 10 is removed, and then wet development or dry development with a developer such as an alkaline aqueous solution, an aqueous developer, or an organic solvent. The resist pattern can be formed by removing the unexposed part and developing the film.

上記アルカリ性水溶液としては、例えば、0.1〜5重量%炭酸ナトリウムの希薄溶液、0.1〜5重量%炭酸カリウムの希薄溶液、0.1〜5重量%水酸化ナトリウムの希薄溶液等が挙げられる。上記アルカリ性水溶液のpHは9〜11の範囲とすることが好ましく、その温度は、感光性樹脂組成物層の現像性に合わせて調節される。また、アルカリ性水溶液中には、表面活性剤、消泡剤、有機溶剤等を混入させてもよい。上記現像の方式としては、例えば、ディップ方式、スプレー方式、ブラッシング、スラッピング等が挙げられる。   Examples of the alkaline aqueous solution include a dilute solution of 0.1 to 5 wt% sodium carbonate, a dilute solution of 0.1 to 5 wt% potassium carbonate, a dilute solution of 0.1 to 5 wt% sodium hydroxide, and the like. It is done. The pH of the alkaline aqueous solution is preferably in the range of 9 to 11, and the temperature is adjusted according to the developability of the photosensitive resin composition layer. Further, a surfactant, an antifoaming agent, an organic solvent, or the like may be mixed in the alkaline aqueous solution. Examples of the development method include a dip method, a spray method, brushing, and slapping.

現像後の処理として、必要に応じて60〜250℃程度の加熱又は0.2〜10J/cm程度の露光を行うことによりレジストパターンをさらに硬化して用いてもよい。本実施形態の感光性エレメントを用いてプリント配線板を製造する場合、現像されたレジストパターンをマスクとして銅めっきで処理する。 As the treatment after development, the resist pattern may be further cured and used by heating at about 60 to 250 ° C. or exposure at about 0.2 to 10 J / cm 2 as necessary. When manufacturing a printed wiring board using the photosensitive element of this embodiment, it processes by copper plating by using the developed resist pattern as a mask.

次いで、レジストパターンは、例えば、現像に用いたアルカリ性水溶液よりさらに強アルカリ性の水溶液で剥離することができる。上記強アルカリ性の水溶液としては、例えば、1〜10重量%水酸化ナトリウム水溶液、1〜10重量%水酸化カリウム水溶液等が用いられる。上記剥離方式としては、例えば、浸漬方式、スプレー方式等が挙げられる。   Next, the resist pattern can be peeled with a stronger alkaline aqueous solution than the alkaline aqueous solution used for development, for example. As said strong alkaline aqueous solution, 1-10 weight% sodium hydroxide aqueous solution, 1-10 weight% potassium hydroxide aqueous solution, etc. are used, for example. Examples of the peeling method include an immersion method and a spray method.

(プリント配線板の製造方法)
本実施形態のプリント配線板の製造方法は、上記レジストパターンの形成方法によりレジストパターンの形成された基板に対し、エッチング処理又はめっき処理することによって行われる。ここで、基板のエッチング処理又はめっき処理は、現像されたレジストパターンをマスクとして、基板の表面を公知の方法によりエッチング又はめっきすることによって行われる。
本発明の感光性樹脂組成物は、中でも、薄型化が要求されるパッケージ用基材やフレキシブルプリント配線板用銅張積層板上に回路を形成する際に好適に使用することができる。
(Printed wiring board manufacturing method)
The manufacturing method of the printed wiring board of this embodiment is performed by performing an etching process or a plating process with respect to the board | substrate with which the resist pattern was formed by the formation method of the said resist pattern. Here, the etching process or the plating process of the substrate is performed by etching or plating the surface of the substrate by a known method using the developed resist pattern as a mask.
Especially the photosensitive resin composition of this invention can be used suitably when forming a circuit on the base material for packages and the copper clad laminated board for flexible printed wiring boards by which thickness reduction is requested | required.

エッチングに用いられるエッチング液としては、例えば、塩化第二銅溶液、塩化第二鉄溶液、アルカリエッチング溶液を用いることができる。めっきとしては、例えば、銅めっき、はんだめっき、ニッケルめっき、金めっきが挙げられる。   As an etching solution used for etching, for example, a cupric chloride solution, a ferric chloride solution, or an alkaline etching solution can be used. Examples of the plating include copper plating, solder plating, nickel plating, and gold plating.

エッチング又はめっきを行った後、レジストパターンは、例えば、現像に用いたアルカリ性水溶液より更に強アルカリ性の水溶液で剥離することができる。この強アルカリ性の水溶液としては、例えば、1〜10質量%水酸化ナトリウム水溶液、1〜10質量%水酸化カリウム水溶液等が用いられる。また、剥離方式としては、例えば、浸漬方式、スプレー方式等が挙げられる。なお、レジストパターンが形成されたプリント配線板は、多層プリント配線板でもよく、小径スルーホールを有していてもよい。   After etching or plating, the resist pattern can be peeled off with a stronger alkaline aqueous solution than the alkaline aqueous solution used for development, for example. As this strongly alkaline aqueous solution, for example, a 1 to 10% by mass sodium hydroxide aqueous solution, a 1 to 10% by mass potassium hydroxide aqueous solution and the like are used. Moreover, as a peeling system, an immersion system, a spray system, etc. are mentioned, for example. The printed wiring board on which the resist pattern is formed may be a multilayer printed wiring board or may have a small diameter through hole.

また、めっきが絶縁層と絶縁層上に形成された導体層とを備えた回路形成用基板に対して行われた場合には、パターン以外の導体層を除去する必要がある。この除去方法としては、例えば、レジストパターンを剥離した後に軽くエッチングする方法や、上記めっきに続いてはんだめっき等を行い、その後レジストパターンを剥離することで配線部分をはんだでマスクし、次いで導体層のみをエッチング可能なエッチング液を用いて処理する方法が挙げられる。   In addition, when plating is performed on a circuit forming substrate including an insulating layer and a conductor layer formed on the insulating layer, it is necessary to remove the conductor layer other than the pattern. As this removal method, for example, a method of lightly etching after removing the resist pattern, or performing solder plating after the above plating, and then masking the wiring portion with solder by peeling off the resist pattern, and then conducting layer The method of processing using the etching liquid which can etch only is mentioned.

本実施形態の感光性樹脂組成物は、上述したように、プリント配線板の製造に好適に使用することができる。即ち、本発明の好適な実施形態の一つは、(A)バインダーポリマー、(B)エチレン性不飽和結合を有する光重合性化合物、及び(C)光重合開始剤を含有する感光性樹脂組成物であって、上記(A)成分が、(a1)ベンジル(メタ)アクリレート誘導体由来の構成単位を50〜80質量%、(a2)スチレン誘導体由来の構成単位を5〜40質量%、(a3)(メタ)アクリル酸アルキルエステル由来の構成単位を1〜20質量%、及び(a4)(メタ)アクリル酸由来の構成単位を5〜30質量%含む、感光性樹脂組成物のプリント配線板の製造への応用である。   The photosensitive resin composition of this embodiment can be used suitably for manufacture of a printed wiring board as mentioned above. That is, one preferred embodiment of the present invention is a photosensitive resin composition containing (A) a binder polymer, (B) a photopolymerizable compound having an ethylenically unsaturated bond, and (C) a photopolymerization initiator. The component (A) is 50 to 80% by mass of the structural unit derived from the (a1) benzyl (meth) acrylate derivative, (a2) 5 to 40% by mass of the structural unit derived from the styrene derivative, (a3 ) A printed wiring board of a photosensitive resin composition containing 1 to 20% by mass of a structural unit derived from (meth) acrylic acid alkyl ester and 5 to 30% by mass of a structural unit derived from (a4) (meth) acrylic acid. Application to manufacturing.

以下、本発明を実施例によりさらに詳細に説明するが、本発明は以下の実施例に何ら限定されるものではない。   EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited to a following example at all.

(実施例1〜5及び比較例1〜4)
(感光性樹脂組成物溶液の調製)
表1に示す(A)成分、(B)成分、(C)成分、添加剤及び溶剤を配合し、感光性樹脂組成物溶液を得た。なお、(A)成分におけるバインダーポリマーは下記の方法により得られたものである。
(Examples 1-5 and Comparative Examples 1-4)
(Preparation of photosensitive resin composition solution)
(A) component shown in Table 1, (B) component, (C) component, the additive, and the solvent were mix | blended, and the photosensitive resin composition solution was obtained. In addition, the binder polymer in (A) component is obtained by the following method.

[バインダーポリマーの合成]
表2に示す(a1)〜(a4)の重合性単量体にアゾビスイソブチロニトリル0.6gを溶解した混合液を「溶液a」とした。
[Synthesis of binder polymer]
A solution obtained by dissolving 0.6 g of azobisisobutyronitrile in the polymerizable monomers (a1) to (a4) shown in Table 2 was designated as “Solution a”.

撹拌機、還流冷却器、温度計、滴下ロート及び窒素ガス導入管を備えたフラスコに、メチルセロソルブ60g及びトルエン40gの混合液(質量比3:2)100gを投入し、フラスコ内に窒素ガスを吹き込みつつ撹拌しながら加熱し、80℃まで昇温させた。   A flask equipped with a stirrer, reflux condenser, thermometer, dropping funnel and nitrogen gas introduction tube was charged with 100 g of a mixture of 60 g of methyl cellosolve and 40 g of toluene (mass ratio 3: 2), and nitrogen gas was introduced into the flask. The mixture was heated with stirring while being blown, and the temperature was raised to 80 ° C.

フラスコ内の上記混合液に、上記溶液aを4時間かけて滴下した後、メチルセロソルブ6g及びトルエン4gの混合液(質量比3:2)で滴下ロートを洗浄しながら10分間かけて滴下し、撹拌しながら80℃にて2時間保温した。次いで、フラスコ内の溶液に、メチルセロソルブ6g及びトルエン4gの混合液(質量比3:2)にアゾビスイソブチロニトリル0.2gを溶解した溶液を10分間かけて滴下した後、メチルセロソルブ18g及びトルエン12gの混合液(質量比3:2)を10分間かけて滴下し、フラスコ内の溶液を撹拌しながら80℃にて3時間保温した。さらに、フラスコ内の溶液を30分間かけて90℃まで昇温させ、90℃にて2時間保温した後、冷却してそれぞれのバインダーポリマーの溶液を得た。   After dropping the solution a over 4 hours into the mixed solution in the flask, the solution was dropped over 10 minutes while washing the dropping funnel with a mixed solution of 6 g of methyl cellosolve and 4 g of toluene (mass ratio 3: 2), The mixture was kept at 80 ° C. for 2 hours while stirring. Next, a solution obtained by dissolving 0.2 g of azobisisobutyronitrile in a mixed liquid of 6 g of methyl cellosolve and 4 g of toluene (mass ratio 3: 2) was dropped into the solution in the flask over 10 minutes, and then 18 g of methyl cellosolve was added. And 12 g of toluene (mass ratio 3: 2) was added dropwise over 10 minutes, and the solution in the flask was kept at 80 ° C. for 3 hours while stirring. Further, the solution in the flask was heated to 90 ° C. over 30 minutes, kept at 90 ° C. for 2 hours, and then cooled to obtain a solution of each binder polymer.

なお、重量平均分子量は、ゲルパーミエーションクロマトグラフィー法(GPC)によって測定し、標準ポリスチレンの検量線を用いて換算することにより導出した。GPCの条件を以下に示す。
GPC条件
ポンプ:日立 L−6000型((株)日立製作所製)
カラム:以下の計3本
Gelpack GL−R420
Gelpack GL−R430
Gelpack GL−R440(以上、日立化成工業(株)製、商品名)
溶離液:テトラヒドロフラン
測定温度:40℃
流量:2.05mL/分
検出器:日立 L−3300型RI((株)日立製作所製)
The weight average molecular weight was measured by gel permeation chromatography (GPC) and derived by conversion using a standard polystyrene calibration curve. The GPC conditions are shown below.
GPC condition pump: Hitachi L-6000 type (manufactured by Hitachi, Ltd.)
Column: The following three Gelpack GL-R420
Gelpack GL-R430
Gelpack GL-R440 (above, manufactured by Hitachi Chemical Co., Ltd., trade name)
Eluent: Tetrahydrofuran Measurement temperature: 40 ° C
Flow rate: 2.05 mL / min Detector: Hitachi L-3300 type RI (manufactured by Hitachi, Ltd.)

(酸価測定)
三角フラスコに合成したバインダーポリマーの溶液0.5gを秤量し、混合溶剤(質量比:トルエン/メタノール=70/30)30mlを加え溶解後、指示薬としてフェノールフタレイン溶液を添加し、N/10水酸化カリウムアルコール溶液で滴定し、酸価を測定した。

Figure 0005935462
(Acid value measurement)
0.5 g of the binder polymer solution synthesized in the Erlenmeyer flask was weighed, dissolved by adding 30 ml of a mixed solvent (mass ratio: toluene / methanol = 70/30), added with a phenolphthalein solution as an indicator, and N / 10 water The acid value was measured by titration with a potassium oxide alcohol solution.
Figure 0005935462

BPE−500:平均10モルのポリオキシエチレンを有するビスフェノールA系ジメタクリレート(新中村化学(株)製、商品名)
BPE−200:平均4モルのポリオキシエチレンを有するビスフェノールA系ジメタクリレート(新中村化学(株)製、商品名)
FA−023M:平均12モルのポリオキシプロピレンの両端に平均3モルのポリオキシエチレンを付与したジメタクリレート(日立化成工業(株)製、商品名)
BPE-500: Bisphenol A dimethacrylate having an average of 10 moles of polyoxyethylene (trade name, manufactured by Shin-Nakamura Chemical Co., Ltd.)
BPE-200: Bisphenol A dimethacrylate having an average of 4 moles of polyoxyethylene (trade name, manufactured by Shin-Nakamura Chemical Co., Ltd.)
FA-023M: Dimethacrylate (trade name, manufactured by Hitachi Chemical Co., Ltd.) with an average of 3 mol of polyoxyethylene added to both ends of an average of 12 mol of polyoxypropylene

Figure 0005935462
Figure 0005935462

(感光性エレメントの作製)
次に、得られた感光性樹脂組成物溶液を、16μm厚のポリエチレンテレフタレートフィルム(帝人(株)製、商品名「G2−16」)上に均一に塗布し、100℃の熱風対流式乾燥機で10分間乾燥した後、28μm厚のポリエチレンフィルム(タマポリ(株)製、商品名「NF−15A」)で保護し感光性エレメントを得た。感光性樹脂組成物層の乾燥後の膜厚は15μmであった。
(Production of photosensitive element)
Next, the obtained photosensitive resin composition solution was uniformly applied onto a 16 μm-thick polyethylene terephthalate film (trade name “G2-16” manufactured by Teijin Limited), and a hot air convection dryer at 100 ° C. After drying for 10 minutes, the film was protected with a 28 μm thick polyethylene film (trade name “NF-15A” manufactured by Tamapoly Co., Ltd.) to obtain a photosensitive element. The film thickness after drying of the photosensitive resin composition layer was 15 μm.

(レジストパターンの形成)
次に、プリント配線板用銅張積層板(日立化成工業(株)製、商品名「MCL−E679」)の銅表面を粗化、アルカリ脱脂、酸洗浄、水洗を実施後、空気流で乾燥し、得られた基材を80℃に加温した。その銅表面上に上記感光性樹脂組成物層をポリエチレンフィルムを剥がしながら100℃のヒートロールを用い1m/分の速度でラミネートし、評価用積層体を得た。
(Formation of resist pattern)
Next, the copper surface of the copper-clad laminate for printed wiring boards (trade name “MCL-E679”, manufactured by Hitachi Chemical Co., Ltd.) is roughened, alkali degreased, acid washed, washed with water, and then dried in an air stream. The obtained substrate was heated to 80 ° C. The photosensitive resin composition layer was laminated on the copper surface at a speed of 1 m / min using a heat roll at 100 ° C. while peeling off the polyethylene film to obtain a laminate for evaluation.

<光感度の評価>
上記評価用積層体上に、ネガとしてストーファー21段ステップタブレットを密着させ、高圧水銀灯ランプを有する露光機(オーク(株)製、商品名「EXM−1201」)を用いて露光を行った。次いで、ポリエチレンテレフタレートフィルムを剥離し、30℃で1重量%炭酸ナトリウム水溶液をスプレーし(スプレー(現像)時間:最少現像時間の2倍)、未露光部分を除去した。その後、銅張積層板上に形成された光硬化膜のステップタブレットの段数(X/21)を測定し、ST=5/21を示す露光量(mJ/cm)を光感度の値とした。この数値が小さいほど、光感度が高いことを示す。
<Evaluation of photosensitivity>
On the evaluation laminate, a 21-step stove tablet was adhered as a negative, and exposure was performed using an exposure machine (trade name “EXM-1201” manufactured by Oak Co., Ltd.) having a high-pressure mercury lamp lamp. Subsequently, the polyethylene terephthalate film was peeled off and sprayed with a 1% by weight sodium carbonate aqueous solution at 30 ° C. (spray (development) time: twice the minimum development time) to remove unexposed portions. Thereafter, the number of steps (X / 21) of the step tablet of the photocured film formed on the copper clad laminate was measured, and the exposure amount (mJ / cm 2 ) indicating ST = 5/21 was defined as the value of the photosensitivity. . It shows that photosensitivity is so high that this figure is small.

<密着性の評価>
上記評価用積層体上にネガとしてライン幅が1〜30(単位:μm)の配線パターンを有するガラス製フォトツールを密着させ、現像後の残存ステップ段数がST=5/21となるエネルギー量によりパターン露光した。次いで、ポリエチレンテレフタレートフィルムを剥離し、30℃で1重量%炭酸ナトリウム水溶液をスプレーし(スプレー(現像)時間:最少現像時間の2倍)、未露光部分を除去した。その後、光学顕微鏡を用いて観察し、密着性の評価を行った。密着性の値は、現像処理によって剥離せずに残ったライン幅(μm)のうち最も小さい値で表され、この数値が小さいほど、密着性が高いことを示す。
<Evaluation of adhesion>
A glass phototool having a wiring pattern with a line width of 1 to 30 (unit: μm) as a negative is adhered to the evaluation laminate, and the number of remaining steps after development is ST = 5/21. The pattern was exposed. Subsequently, the polyethylene terephthalate film was peeled off and sprayed with a 1% by weight sodium carbonate aqueous solution at 30 ° C. (spray (development) time: twice the minimum development time) to remove unexposed portions. Then, it observed using the optical microscope and evaluated adhesiveness. The adhesion value is represented by the smallest value of the line width (μm) remaining without being peeled off by the development process, and the smaller this value, the higher the adhesion.

<解像性の評価>
上記評価用積層体上にネガとしてライン幅/スペース幅が1/1〜30/30(単位:μm)の配線パターンを有するガラス製フォトツールを密着させ、現像後の残存ステップ段数がST=5/21となるエネルギー量によりパターン露光した。次いで、ポリエチレンテレフタレートフィルムを剥離し、30℃で1重量%炭酸ナトリウム水溶液をスプレーし(スプレー(現像)時間:最少現像時間の2倍)、未露光部分を除去した。その後、光学顕微鏡を用いて観察し、解像性の評価を行った。解像性の値は、現像処理によって未露光部を完全に除去できたスペース幅(μm)のうち最も小さい値で表され、この数値が小さい程、解像性が高いことを示す。
<Evaluation of resolution>
A glass phototool having a wiring pattern with a line width / space width of 1/1 to 30/30 (unit: μm) as a negative is brought into close contact with the evaluation laminate, and the number of remaining steps after development is ST = 5. Pattern exposure was performed with an energy amount of / 21. Subsequently, the polyethylene terephthalate film was peeled off and sprayed with a 1% by weight sodium carbonate aqueous solution at 30 ° C. (spray (development) time: twice the minimum development time) to remove unexposed portions. Then, it observed using the optical microscope and evaluated resolution. The value of the resolution is represented by the smallest value among the space widths (μm) in which the unexposed portions can be completely removed by the development processing, and the smaller the numerical value, the higher the resolution.

<めっき耐性の評価>
感光性樹脂組成物層をフレキシブルプリント配線板用銅張積層板(ニッカン工業(株)製、商品名「F30VC1」)にラミネートし作成した評価用積層体上にネガとして1/1〜30/30(単位:μm)の配線パターンを有するガラス製フォトツールを密着させ、現像後の残存ステップ段数がST=5/21となるエネルギー量によりパターン露光した。次いで、ポリエチレンテレフタレートフィルムを剥離し、30℃で1重量%炭酸ナトリウム水溶液をスプレーし(スプレー(現像)時間:最少現像時間の2倍)、未露光部分を除去し、評価用基板を得た。上記評価用基板に酸脱脂、水洗、硫酸ディップを順に実施し、硫酸銅めっき液を用いて1A/dmの条件でめっき厚みが12μmになるまで銅めっき処理を行った。水洗、乾燥後、レジストを剥離し、上方から光学顕微鏡を用いて、めっきもぐり幅を測定した。めっき耐性の値は、めっきもぐり幅で評価され、数値が小さいほど銅めっき耐性が良好であることを示す。
<Evaluation of plating resistance>
1 / 1-30 / 30 as a negative on a laminate for evaluation prepared by laminating a photosensitive resin composition layer on a copper-clad laminate for flexible printed wiring boards (trade name “F30VC1” manufactured by Nikkan Kogyo Co., Ltd.). A glass phototool having a wiring pattern of (unit: μm) was brought into close contact, and pattern exposure was performed with an energy amount such that the number of remaining steps after development was ST = 5/21. Next, the polyethylene terephthalate film was peeled off, and a 1 wt% aqueous sodium carbonate solution was sprayed at 30 ° C. (spray (development) time: twice the minimum development time) to remove the unexposed portion and obtain a substrate for evaluation. The substrate for evaluation was subjected to acid degreasing, water washing, and sulfuric acid dipping in this order, and copper plating treatment was performed using a copper sulfate plating solution until the plating thickness reached 12 μm under the condition of 1 A / dm 2 . After washing with water and drying, the resist was peeled off, and the plating boring width was measured from above using an optical microscope. The value of the plating resistance is evaluated by the plating width, and the smaller the numerical value, the better the copper plating resistance.

<屈曲性>
感光性樹脂組成物層をフレキシブルプリント配線板用銅張積層板(ニッカン工業(株)製、商品名「F30VC1」)にラミネートし作成した評価用積層体を30mm×150mm四方の大きさに切断し、現像後の残存ステップ段数がST=5/21となるエネルギー量により全面露光した。次いで、ポリエチレンテレフタレートフィルムを剥離し、30℃で1重量%炭酸ナトリウム水溶液をスプレーした(スプレー(現像)時間:最少現像時間の2倍)。得られたサンプルをガードナー式マンドレル屈曲試験機でレジストに亀裂が発生しない最大直径を測定した。直径が小さいほど、屈曲性が良好であることを示す。
<Flexibility>
The laminate for evaluation prepared by laminating the photosensitive resin composition layer on a copper-clad laminate for flexible printed wiring boards (product name “F30VC1” manufactured by Nikkan Kogyo Co., Ltd.) was cut into a 30 mm × 150 mm square size. The entire surface was exposed with an energy amount such that the number of remaining steps after development was ST = 5/21. Next, the polyethylene terephthalate film was peeled off and sprayed with a 1% by weight sodium carbonate aqueous solution at 30 ° C. (spray (development) time: twice the minimum development time). The maximum diameter at which the resist did not crack was measured with the Gardner mandrel bending tester. The smaller the diameter, the better the flexibility.

Figure 0005935462
Figure 0005935462

表3から明らかなように、本発明の感光性樹脂組成物を用いた実施例1〜5は、屈曲性、めっき耐性に優れ、且つ充分な光感度、密着性及び解像性を示す。   As is apparent from Table 3, Examples 1 to 5 using the photosensitive resin composition of the present invention are excellent in flexibility and plating resistance, and exhibit sufficient photosensitivity, adhesion and resolution.

1…感光性エレメント、10…支持フィルム、20…感光性樹脂組成物層。   DESCRIPTION OF SYMBOLS 1 ... Photosensitive element, 10 ... Support film, 20 ... Photosensitive resin composition layer.

Claims (3)

支持フィルムと、該支持フィルム上に形成される感光性樹脂組成物からなる感光性樹脂組成物層と、を備える感光性エレメントであって、
前記感光性樹脂組成物は、(A)バインダーポリマー、(B)エチレン性不飽和結合を有する光重合性化合物、及び(C)光重合開始剤を含有し、
前記(A)成分は、(a1)ベンジル(メタ)アクリレート誘導体由来の構成単位を50〜80質量%、(a2)スチレン誘導体由来の構成単位を5〜40質量%、(a3)(メタ)アクリル酸アルキルエステル由来の構成単位を1〜20質量%、及び(a4)(メタ)アクリル酸由来の構成単位を5〜30質量%含む、感光性エレメント。
A support film, a photosensitive element comprising a photosensitive resin composition layer composed of a photosensitive light-sensitive resin composition that will be formed on the support film,
The photosensitive resin composition contains (A) a binder polymer, (B) a photopolymerizable compound having an ethylenically unsaturated bond, and (C) a photopolymerization initiator,
The component (A) includes (a1) 50 to 80% by mass of a structural unit derived from a benzyl (meth) acrylate derivative, (a2) 5 to 40% by mass of a structural unit derived from a styrene derivative, and (a3) (meth) acrylic. A photosensitive element comprising 1 to 20% by mass of a structural unit derived from an acid alkyl ester and 5 to 30% by mass of a structural unit derived from (a4) (meth) acrylic acid.
請求項に記載の感光性エレメントを、前記感光性樹脂組成物層、前記支持フィルムの順に基板上に積層する積層工程と、
前記感光性樹脂組成物層に光硬化部を形成させる露光工程と、
前記光硬化部以外の前記感光性樹脂組成物層を除去する現像工程と、
を含む、レジストパターンの形成方法。
A lamination step of laminating the photosensitive element according to claim 1 on the substrate in the order of the photosensitive resin composition layer and the support film;
An exposure step of forming a photocured portion in the photosensitive resin composition layer;
A developing step for removing the photosensitive resin composition layer other than the photocured portion;
A method for forming a resist pattern, comprising:
請求項に記載のレジストパターンの形成方法によりレジストパターンが形成される基板に対し、エッチング処理又はめっき処理を施す、プリント配線板の製造方法。 A method for producing a printed wiring board, comprising subjecting a substrate on which a resist pattern is formed by the method for forming a resist pattern according to claim 2 , to etching or plating.
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KR20130014615A (en) * 2008-03-21 2013-02-07 히다치 가세고교 가부시끼가이샤 Photosensitive resin composition, photosensitive element, method of forming resist pattern, and process for producing printed wiring board
CN101738861B (en) * 2008-11-10 2012-07-25 日立化成工业株式会社 Light-sensitive resin composite and method for manufacturing printed circuit board using same
CN103543608A (en) * 2009-02-26 2014-01-29 日立化成工业株式会社 Photosensitive resin composition, and photosensitive element, resist pattern formation method and printed circuit board production method each utilizing same
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