JP2017161636A - Photosensitive resin composition, dry film, and printed wiring board - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a photosensitive resin composition which is capable of obtaining excellent developability and allows an outer surface of a cured product thereof to be satisfactorily roughened in a previous step of plating, thereby improving adhesion between the cured product and a plating layer.SOLUTION: The photosensitive resin composition contains a carboxyl group-containing resin (A), an unsaturated compound (B) having at least one ethylenically unsaturated bond in one molecule, a photopolymerization initiator (C), an epoxy compound (D), an organic filler (E) containing an organic filler (E1) having a carboxyl group, and at least one melamine compound (F) selected from the group consisting of melamine and melamine derivatives.SELECTED DRAWING: Figure 1

Description

  The present invention relates to a photosensitive resin composition, a dry film, and a printed wiring board. Specifically, an electrically insulating layer such as a solder resist layer, a plating resist layer, an etching resist layer, or an interlayer insulating layer is formed on the printed wiring board. A photosensitive resin composition suitable for the above, a dry film containing the photosensitive resin composition, a printed wiring board including an interlayer insulating layer containing a cured product of the photosensitive resin composition, and the photosensitive resin composition The present invention relates to a printed wiring board having a solder resist layer containing a cured product.

  Conventionally, various curable resin compositions have been used to form electrically insulating layers such as solder resist layers, plating resist layers, etching resist layers, and interlayer insulating layers of printed wiring boards. Such a resin composition is, for example, a photosensitive resin composition.

  In order to give high heat resistance to the layer formed from the photosensitive resin composition, a photosensitive resin composition containing a carboxyl group-containing resin has been proposed (for example, Patent Document 1).

  When forming a plating layer on a layer made of a cured product of such a photosensitive resin composition, the surface of the cured product layer of the photosensitive resin composition contains, for example, potassium permanganate in the previous step of the plating treatment. Oxidizing agent may roughen. However, when the cured product layer is treated with the oxidizing agent, the surface of the cured product layer is excessively corroded, and the thickness of the layer may be reduced. Although the carboxyl group-containing resin as in Patent Document 1 has a relatively high resistance to the oxidizing agent, even if the photosensitive resin composition contains this carboxyl group-containing resin, the thickness of the cured product layer is not reduced. It may become too thin with the agent.

  Moreover, carboxyl group-containing resin may reduce the developability of the photosensitive resin composition. If the molecular weight of the carboxyl group-containing resin is reduced in order to improve developability, the resistance of the cured product layer to the oxidizing agent is reduced, and the thickness of the cured product layer is further reduced with the oxidizing agent. There is. For this reason, in order to improve the adhesiveness of hardened | cured material and a plating layer, it was difficult to roughen the surface of the hardened | cured material layer of the photosensitive resin composition moderately with the said oxidizing agent.

Japanese Patent No. 4508929

  The object of the present invention is to obtain an excellent developability and to roughen the outer surface of the cured product satisfactorily in the pre-process of the plating treatment. Photosensitive resin composition capable of improving properties, dry film containing the photosensitive resin composition, printed wiring board including an interlayer insulating layer containing a cured product of the photosensitive resin composition, and the photosensitive resin It is providing a printed wiring board provided with the soldering resist layer containing the hardened | cured material of a composition.

  A photosensitive resin composition according to one embodiment of the present invention includes a carboxyl group-containing resin (A), an unsaturated compound (B) having at least one ethylenically unsaturated bond in one molecule, a photopolymerization initiator ( C), an epoxy compound (D), an organic filler (E) containing an organic filler (E1) having a carboxyl group, and at least one melamine compound (F) selected from the group of melamine and melamine derivatives. contains.

  The dry film which concerns on 1 aspect of this invention contains the said photosensitive resin composition.

  The printed wiring board which concerns on 1 aspect of this invention is equipped with the interlayer insulation layer containing the hardened | cured material of the said photosensitive resin composition.

  The printed wiring board which concerns on 1 aspect of this invention is equipped with the soldering resist layer containing the hardened | cured material of the said photosensitive resin composition.

  According to the present invention, excellent developability can be obtained, and the outer surface of the cured product can be satisfactorily roughened in the previous step of the plating treatment. Photosensitive resin composition capable of improving properties, dry film containing the photosensitive resin composition, printed wiring board including an interlayer insulating layer containing a cured product of the photosensitive resin composition, and the photosensitive resin A printed wiring board provided with the soldering resist layer containing the hardened | cured material of a composition is obtained.

1A to 1E are cross-sectional views illustrating steps of manufacturing a multilayer printed wiring board according to an embodiment of the present invention.

  Hereinafter, an embodiment of the present invention will be described. In the following description, “(meth) acryl” means at least one of “acryl” and “methacryl”. For example, (meth) acrylate means at least one of acrylate and methacrylate.

  The photosensitive resin composition according to this embodiment includes a carboxyl group-containing resin (A), an unsaturated compound (B) having at least one ethylenically unsaturated bond in one molecule, and a photopolymerization initiator (C). And an epoxy compound (D), an organic filler (E) containing an organic filler (E1) having a carboxyl group, and at least one melamine compound (F) selected from the group of melamine and melamine derivatives. .

  The carboxyl group-containing resin (A) preferably contains a carboxyl group-containing resin having an aromatic ring. When the carboxyl group-containing resin (A) contains an aromatic ring, high heat resistance and insulation reliability can be imparted to the cured product of the photosensitive resin composition containing the carboxyl group-containing resin (A). It is more preferable that the carboxyl group-containing resin (A) includes a carboxyl group-containing resin having any polycyclic aromatic ring among a biphenyl skeleton, a naphthalene skeleton, a fluorene skeleton, and an anthracene skeleton. The photosensitive resin composition containing carboxyl group-containing resin (A) because carboxyl group-containing resin (A) contains any polycyclic aromatic ring among biphenyl skeleton, naphthalene skeleton, fluorene skeleton, and anthracene skeleton. Higher heat resistance and insulation reliability can be imparted to the cured product. More preferably, the carboxyl group-containing resin (A) includes a carboxyl group-containing resin having a bisphenolfluorene skeleton. When the carboxyl group-containing resin (A) includes a bisphenolfluorene skeleton, higher heat resistance and insulation reliability can be imparted to the cured product of the photosensitive resin composition containing the carboxyl group-containing resin (A).

The carboxyl group-containing resin (A) preferably contains a carboxyl group-containing resin (A1) having a bisphenol fluorene skeleton as described below. The carboxyl group-containing resin (A1) is represented by, for example, the following formula (1), and in the formula (1), R _{1 to} R ₈ are each independently hydrogen, an alkyl group having 1 to 5 carbon atoms or a halogenated bisphenol. It is a reaction product of an intermediate which is a reaction product of an epoxy compound (a1) having a fluorene skeleton and an unsaturated group-containing carboxylic acid (a2), and an acid anhydride (a3). The carboxyl group-containing resin (A1) is obtained by reacting the epoxy compound (a1) having a bisphenolfluorene skeleton represented by the following formula (1) with the unsaturated group-containing carboxylic acid (a2), thereby obtaining the intermediate It is synthesized by reacting the body with an acid anhydride (a3).

In formula (1), R _{1 to} R ₈ are each independently hydrogen, an alkyl group having 1 to 5 carbon atoms, or halogen. That is, each of R _{1 to} R ₈ in Formula (1) may be hydrogen, but may be an alkyl group having 1 to 5 carbon atoms or a halogen. Even if the hydrogen in the aromatic ring is substituted with a low molecular weight alkyl group or halogen, the physical properties of the carboxyl group-containing resin (A1) are not adversely affected. This is because the heat resistance or flame retardancy of the cured product of the conductive resin composition may be improved.

  The carboxyl group-containing resin (A1) can be synthesized, for example, as described below. In order to synthesize the carboxyl group-containing resin (A1), first, at least a part of the epoxy group (see formula (2)) in the epoxy compound (a1) having a bisphenolfluorene skeleton represented by formula (1) and unsaturated An intermediate is synthesized by reacting the group-containing carboxylic acid (a2). The intermediate has a structure represented by the following formula (3) generated by the ring-opening addition reaction between the epoxy group and the unsaturated group-containing carboxylic acid (a2). That is, the intermediate has a secondary hydroxyl group generated by a ring-opening addition reaction between an epoxy group and an unsaturated group-containing carboxylic acid (a2) in the structure represented by the formula (3). In Formula (3), A is an unsaturated group-containing carboxylic acid residue.

  Next, the secondary hydroxyl group in the intermediate is reacted with the acid anhydride (a3). Thereby, carboxyl group-containing resin (A1) can be synthesized.

  The acid anhydride (a3) may contain at least one of acid monoanhydride (a3-1) and acid dianhydride (a3-2). When the acid anhydride (a3) contains acid monoanhydride (a3-1), the carboxyl group-containing resin (A1) has a bisphenolfluorene skeleton represented by the formula (1) and a structure represented by the following formula (4): Have

  The structure represented by the formula (4) is generated by the reaction between the secondary hydroxyl group in the structure represented by the formula (3) of the intermediate and the acid anhydride group in the acid monoanhydride (a3-1). In Formula (4), A is an unsaturated group-containing carboxylic acid residue, and B is an acid monoanhydride residue.

  When the acid anhydride (a3) contains an acid dianhydride (a3-2), the carboxyl group-containing resin (A1) has a bisphenolfluorene skeleton represented by the formula (1) and a structure represented by the following formula (5). And have.

  The structure represented by the formula (5) is generated by a reaction between two acid anhydride groups in the acid dianhydride (a3-2) and two secondary hydroxyl groups in the intermediate. That is, the structure shown in Formula (5) is produced by crosslinking of two secondary hydroxyl groups with acid dianhydride (a3-2). In addition, the case where two secondary hydroxyl groups present in one molecule of the intermediate are crosslinked and the case where two secondary hydroxyl groups present in each of the two molecules of the intermediate are crosslinked It is possible. When two secondary hydroxyl groups present in the two molecules of the intermediate are cross-linked, an increase in molecular weight is obtained. In Formula (5), A is an unsaturated group-containing carboxylic acid residue, and D is an acid dianhydride residue.

  The carboxyl group-containing resin (A1) can be obtained by reacting the secondary hydroxyl group in the intermediate with the acid anhydride (a3). When the acid anhydride (a3) contains an acid monoanhydride (a3-1) and an acid dianhydride (a3-2), a part of the secondary hydroxyl groups in the intermediate and the acid dianhydride ( a3-2) is reacted, and another part of the secondary hydroxyl groups in the intermediate is reacted with acid monoanhydride (a3-1). Thereby, carboxyl group-containing resin (A1) can be synthesized. In this case, the carboxyl group-containing resin (A1) has a bisphenolfluorene skeleton represented by the formula (1), a structure represented by the above formula (4), and a structure represented by the above formula (5).

  The carboxyl group-containing resin (A1) may further have a structure represented by the following formula (6). The structure represented by the formula (6) occurs when only one of the two acid anhydride groups in the acid dianhydride (a3-2) reacts with the secondary hydroxyl group in the intermediate. In Formula (6), A is an unsaturated group-containing carboxylic acid residue, and D is an acid dianhydride residue.

  When some of the epoxy groups in the epoxy compound (a1) remain unreacted during the synthesis of the intermediate, the carboxyl group-containing resin (A1) may have a structure represented by the formula (2), that is, an epoxy group. sell. In addition, when a part of the structure represented by the formula (3) in the intermediate body remains unreacted, the carboxyl group-containing resin (A1) may have a structure represented by the formula (3).

  When the acid anhydride (a3) contains an acid dianhydride (a3-2), by optimizing the reaction conditions during the synthesis of the carboxyl group-containing resin (A1), the carboxyl group-containing resin (A1) The structure shown in Formula (2) and the structure shown in Formula (6) can be reduced or almost eliminated.

  As described above, the carboxyl group-containing resin (A1) has a bisphenolfluorene skeleton represented by the formula (1), and the acid anhydride (a3) contains an acid monoanhydride (a3-1). When it has the structure shown in (4) and the acid anhydride (a3) contains acid dianhydride (a3-2), it can have the structure shown in Formula (5). Further, when the acid anhydride (a3) contains an acid monoanhydride (a3-1), the carboxyl group-containing resin (A1) has a structure represented by the formula (2) and a structure represented by the formula (3). May have at least one. When the acid anhydride (a3) contains an acid dianhydride (a3-2), the carboxyl group-containing resin (A1) has a structure represented by the formula (2) and a structure represented by the formula (6). May have at least one of them. Furthermore, when the acid anhydride (a3) contains an acid monoanhydride (a3-1) and an acid dianhydride (a3-2), the carboxyl group-containing resin (A1) has a structure represented by the formula (2). And at least one of the structure represented by formula (3) and the structure represented by formula (6).

  When the epoxy compound (a1) itself has a secondary hydroxyl group, that is, for example, when n = 1 or more in the formula (7) described later, the carboxyl group-containing resin (A1) is an epoxy compound (a1). The secondary secondary hydroxyl group and the acid anhydride (a3) may react with each other.

  In addition, the structure of the above-mentioned carboxyl group-containing resin (A1) is reasonably inferred based on the common general technical knowledge, and the structure of the carboxyl group-containing resin (A1) cannot be identified by analysis. The reason is as follows. When the epoxy compound (a1) itself has a secondary hydroxyl group (for example, when n is 1 or more in the formula (7)), the carboxyl group-containing resin depends on the number of secondary hydroxyl groups in the epoxy compound (a1). The structure of (A1) changes greatly. Further, when the intermediate and the acid dianhydride (a3-2) react, as described above, two secondary hydroxyl groups present in one molecule of the intermediate form an acid dianhydride (a3). -2) and two secondary hydroxyl groups present in the two molecules of the intermediate can be crosslinked with acid dianhydride (a3-2). For this reason, the carboxyl group-containing resin (A1) finally obtained contains a plurality of molecules having different structures, and even when the carboxyl group-containing resin (A1) is analyzed, the structure cannot be identified.

  The carboxyl group-containing resin (A1) has photoreactivity by having an ethylenically unsaturated group derived from the unsaturated group-containing carboxylic acid (a2). For this reason, carboxyl group-containing resin (A1) can provide photosensitivity, specifically, ultraviolet curability, to the photosensitive resin composition. Moreover, carboxyl group-containing resin (A1) has a carboxyl group derived from an acid anhydride (a3), so that the photosensitive resin composition contains at least one of an alkali metal salt and an alkali metal hydroxide. The developability by alkaline aqueous solution can be provided. Furthermore, when the acid anhydride (a3) contains an acid dianhydride (a3-2), the carboxyl group-containing resin (A1) has a molecular weight that is crosslinked by the acid dianhydride (a3-2). It has been adjusted. For this reason, the carboxyl group-containing resin (A1) in which the acid value and the molecular weight are appropriately adjusted is obtained. When the acid anhydride (a3) contains an acid monoanhydride (a3-1) and an acid dianhydride (a3-2), the acid monoanhydride (a3-1) and the acid dianhydride (a3-2) And the amount of the acid monoanhydride (a3-1) relative to the acid dianhydride (a3-2) can be easily adjusted to adjust the molecular weight and the acid value of the carboxyl group-containing resin (A1).

  The weight average molecular weight of the carboxyl group-containing resin (A1) is preferably in the range of 700 to 10,000. When the weight average molecular weight is 700 or more, the tackiness of the film formed from the photosensitive resin composition can be further suppressed, and the insulation reliability and plating resistance of the cured product can be further improved. Moreover, the developability by the alkaline aqueous solution of the photosensitive resin composition improves especially that a weight average molecular weight is 10,000 or less. The weight average molecular weight is more preferably in the range of 900 to 8000, and particularly preferably in the range of 1000 to 5000.

  The solid content acid value of the carboxyl group-containing resin (A1) is preferably in the range of 60 to 140 mgKOH / g. In this case, the developability of the photosensitive resin composition is particularly improved. The acid value is more preferably in the range of 80 to 135 mgKOH / g, and the acid value is more preferably in the range of 90 to 130 mgKOH / g.

  The polydispersity of the carboxyl group-containing resin (A1) may be in the range of 1.0 to 4.8. In this case, excellent developability can be imparted to the photosensitive resin composition while ensuring good insulation reliability of the cured product formed from the photosensitive resin composition. The polydispersity is more preferably 1.1 to 4.0, and still more preferably 1.2 to 2.8. The polydispersity is a value (Mw / Mn) of the ratio of the weight average molecular weight (Mw) to the number average molecular weight (Mn) of the carboxyl group-containing resin (A1).

  The weight average molecular weight (Mw) of the carboxyl group-containing resin (A1) is calculated from the molecular weight measurement result by gel permeation chromatography. The molecular weight measurement by gel permeation chromatography can be performed, for example, under the following conditions.

GPC device: SHODEX SYSTEM 11, manufactured by Showa Denko KK
Column: 4 series of SHODEX KF-800P, KF-005, KF-003, KF-001,
Mobile phase: THF,
Flow rate: 1 ml / min
Column temperature: 45 ° C
Detector: RI,
Conversion: Polystyrene.

  The raw material of the carboxyl group-containing resin (A1) and the reaction conditions during the synthesis of the carboxyl group-containing resin (A1) will be described in detail.

  The epoxy compound (a1) has a structure represented by the following formula (7), for example. N in Formula (7) is a number within the range of 0-20, for example. In order to appropriately control the molecular weight of the carboxyl group-containing resin (A1), the average of n is particularly preferably in the range of 0-1. If the average of n is in the range of 0 to 1, particularly when the acid anhydride (a3) contains the acid dianhydride (a3-2), an excess due to the addition of the acid dianhydride (a3-2) Increase in molecular weight tends to be suppressed.

  The unsaturated group-containing carboxylic acid (a2) can contain, for example, a compound having only one ethylenically unsaturated group in one molecule. More specifically, the unsaturated group-containing carboxylic acid (a2) is, for example, acrylic acid, methacrylic acid, ω-carboxy-polycaprolactone (n≈2) monoacrylate, crotonic acid, cinnamic acid, 2-acryloyloxyethyl succinate. Acid, 2-methacryloyloxyethyl succinic acid, 2-acryloyloxyethyl phthalic acid, 2-methacryloyloxyethyl phthalic acid, 2-acryloyloxypropyl phthalic acid, 2-methacryloyloxypropyl phthalic acid, 2-acryloyloxyethyl maleic acid, 2-methacryloyloxyethyl maleic acid, β-carboxyethyl acrylate, 2-acryloyloxyethyl tetrahydrophthalic acid, 2-methacryloyloxyethyl tetrahydrophthalic acid, 2-acryloyloxyethyl hexahydrophthalic acid And one or more compounds selected from the group consisting of 2-methacryloyloxyethyl hexahydrophthalic acid. Preferably, unsaturated group containing carboxylic acid (a2) contains acrylic acid.

  In reacting the epoxy compound (a1) with the unsaturated group-containing carboxylic acid (a2), a known method may be employed. For example, a reactive solution is obtained by adding an unsaturated group-containing carboxylic acid (a2) to a solvent solution of the epoxy compound (a1), and further adding a thermal polymerization inhibitor and a catalyst as necessary and stirring and mixing. An intermediate can be obtained by reacting this reactive solution in a conventional manner, preferably at a temperature of 60 to 150 ° C., particularly preferably at a temperature of 80 to 120 ° C. Solvents include, for example, ketones such as methyl ethyl ketone and cyclohexanone, and aromatic hydrocarbons such as toluene and xylene, and ethyl acetate, butyl acetate, cellosolve acetate, butyl cellosolve acetate, carbitol acetate, butyl carbitol acetate, propylene glycol monomethyl ether It can contain at least one component selected from the group consisting of acetates such as acetate and dialkyl glycol ethers. The thermal polymerization inhibitor contains, for example, at least one of hydroquinone and hydroquinone monomethyl ether. The catalyst is at least selected from the group consisting of tertiary amines such as benzyldimethylamine and triethylamine, quaternary ammonium salts such as trimethylbenzylammonium chloride and methyltriethylammonium chloride, triphenylphosphine, and triphenylstibine. A kind of component can be contained.

  It is particularly preferred that the catalyst contains triphenylphosphine. That is, it is preferable to react the epoxy compound (a1) with the unsaturated group-containing carboxylic acid (a2) in the presence of triphenylphosphine. In this case, the ring-opening addition reaction between the epoxy group and the unsaturated group-containing carboxylic acid (a2) in the epoxy compound (a1) is particularly accelerated, and the reaction rate (conversion) is 95% or more, 97% or more, or almost 100%. Rate) can be achieved. For this reason, the intermediate which has a structure shown in Formula (3) is obtained with a high yield. Moreover, generation | occurrence | production of the ion migration in the layer containing the hardened | cured material of the photosensitive resin composition is suppressed, and the insulation reliability of the layer containing hardened | cured material further improves.

  When the epoxy compound (a1) and the unsaturated group-containing carboxylic acid (a2) are reacted, the amount of the unsaturated group-containing carboxylic acid (a2) relative to 1 mol of the epoxy group of the epoxy compound (a1) is 0.8 to 1. It is preferably within a range of 2 moles. In this case, excellent photosensitivity and storage stability of the photosensitive resin composition can be obtained.

  It is also preferable to react the epoxy compound (a1) and the unsaturated group-containing carboxylic acid (a2) under air bubbling. In this case, the addition polymerization reaction of the unsaturated group can be suppressed, and the increase in the molecular weight of the intermediate and the gelation of the intermediate solution can be suppressed. Moreover, the excessive coloring of carboxyl group-containing resin (A1) which is a final product can be suppressed.

  The intermediate obtained in this way has a hydroxyl group produced by the reaction of the epoxy group in the epoxy compound (a1) and the carboxyl group in the unsaturated group-containing carboxylic acid (a2).

  The acid monoanhydride (a3-1) is a compound having one acid anhydride group. The acid monoanhydride (a3-1) can contain an anhydride of a dicarboxylic acid. Acid monoanhydride (a3-1) is, for example, phthalic anhydride, 1,2,3,6-tetrahydrophthalic anhydride, methyltetrahydrophthalic anhydride, methylnadic acid anhydride, hexahydrophthalic anhydride, Methyl hexahydrophthalic anhydride, succinic anhydride, methyl succinic anhydride, maleic anhydride, citraconic anhydride, glutaric anhydride, cyclohexane-1,2,4-tricarboxylic acid-1,2-anhydride And one or more compounds selected from the group consisting of itaconic anhydride. In particular, it is preferable that the acid monoanhydride (a3-1) contains 1,2,3,6-tetrahydrophthalic anhydride. That is, it is preferable that the acid anhydride (a3) contains 1,2,3,6-tetrahydrophthalic anhydride. That is, it is preferable that the carboxyl group-containing resin (A1) has a structure represented by the formula (4), and B in the formula (4) includes a 1,2,3,6-tetrahydrophthalic anhydride residue. In this case, while ensuring good developability of the photosensitive resin composition, it is possible to further suppress the tackiness of a film formed from the photosensitive resin composition and further improve the insulation reliability and plating resistance of the cured product. . It is preferable that 1,2,3,6-tetrahydrophthalic anhydride is in the range of 20 to 100 mol%, and in the range of 40 to 100 mol%, based on the entire acid monoanhydride (a3-1). Although it is more preferable that there is, it is not limited to this.

  Acid dianhydride (a3-2) is a compound having two acid anhydride groups. The acid dianhydride (a3-2) can contain an anhydride of tetracarboxylic acid. Examples of the acid dianhydride (a3-2) include 1,2,4,5-benzenetetracarboxylic dianhydride, benzophenone tetracarboxylic dianhydride, methylcyclohexene tetracarboxylic dianhydride, and tetracarboxylic dianhydride. , Naphthalene-1,4,5,8-tetracarboxylic dianhydride, ethylenetetracarboxylic dianhydride, 9,9'-bis (3,4-dicarboxyphenyl) fluorene dianhydride, glycerin bisan Hydrotrimellitate monoacetate, ethylene glycol bisanhydro trimellitate, 3,3 ′, 4,4′-diphenylsulfone tetracarboxylic dianhydride, 1,3,3a, 4,5,9b-hexahydro-5 (Tetrahydro-2,5-dioxo-3-furanyl) naphtho [1,2-c] furan-1,3-dione, 1,2,3,4- Tan tetracarboxylic dianhydride, and 3,3 ', may contain at least one compound selected from the group consisting of 4,4'-biphenyl tetracarboxylic acid dianhydride. In particular, the acid dianhydride (a3-2) preferably contains 3,3 ', 4,4'-biphenyltetracarboxylic dianhydride. That is, it is preferable that D in Formula (5) and Formula (6) includes a 3,3 ′, 4,4′-biphenyltetracarboxylic dianhydride residue. In this case, while ensuring good developability of the photosensitive resin composition, it is possible to further suppress the tackiness of a film formed from the photosensitive resin composition and further improve the insulation reliability and plating resistance of the cured product. . 3,3 ′, 4,4′-biphenyltetracarboxylic dianhydride is preferably in the range of 20 to 100 mol%, and preferably 40 to 100 mol, based on the entire acid dianhydride (a3-2). % Is more preferable, but not limited thereto.

  In reacting the intermediate with the acid anhydride (a3), a known method may be employed. For example, a reactive solution is obtained by adding an acid anhydride (a3) to a solvent solution of an intermediate, further adding a thermal polymerization inhibitor and a catalyst as necessary, and stirring and mixing. The carboxyl group-containing resin (A1) can be obtained by reacting this reactive solution in a conventional manner, preferably at a temperature of 60 to 150 ° C., particularly preferably 80 to 120 ° C. As the solvent, catalyst and polymerization inhibitor, appropriate ones can be used, and the solvent, catalyst and polymerization inhibitor used in the synthesis of the intermediate can also be used as they are.

  It is particularly preferred that the catalyst contains triphenylphosphine. That is, it is preferable to react the intermediate and the acid anhydride (a3) in the presence of triphenylphosphine. In this case, the reaction between the secondary hydroxyl group and the acid anhydride (a3) in the intermediate is particularly accelerated, and a reaction rate (conversion rate) of 90% or more, 95% or more, 97% or more, or almost 100% is achieved. Is possible. For this reason, the carboxyl group-containing resin (A1) having at least one of the structure represented by the formula (4) and the structure represented by the formula (5) can be obtained with high yield. Moreover, generation | occurrence | production of the ion migration in the layer containing the hardened | cured material of the photosensitive resin composition is suppressed, and the insulation reliability of the layer containing hardened | cured material further improves.

  When the acid anhydride (a3) contains the acid dianhydride (a3-2) and the acid monoanhydride (a3-1), the acid dianhydride with respect to 1 mol of the epoxy group of the epoxy compound (a1) The amount of (a3-2) is preferably in the range of 0.05 to 0.24 mol. Moreover, it is preferable that the quantity of acid monoanhydride (a3-1) exists in the range of 0.3-0.7 mol with respect to 1 mol of epoxy groups of an epoxy compound (a1). In this case, the carboxyl group-containing resin (A1) in which the acid value and the molecular weight are appropriately adjusted can be easily obtained.

  The carboxyl group-containing resin (A) may contain only the carboxyl group-containing resin (A1) or only a carboxyl group-containing resin other than the carboxyl group-containing resin (A1), and the carboxyl group-containing resin (A1) and the carboxyl group-containing resin. You may contain carboxyl group-containing resin other than resin (A1). The carboxyl group-containing resin other than the carboxyl group-containing resin (A1) includes a carboxyl group-containing resin having no bisphenolfluorene skeleton (hereinafter also referred to as a carboxyl group-containing resin (A2)).

  The carboxyl group-containing resin (A2) can contain, for example, a compound having a carboxyl group and not having photopolymerizability (hereinafter referred to as (A2-1) component). (A2-1) A component contains the polymer of the ethylenically unsaturated monomer containing the ethylenically unsaturated compound which has a carboxyl group, for example. The ethylenically unsaturated compound having a carboxyl group can contain compounds such as acrylic acid, methacrylic acid, and ω-carboxy-polycaprolactone (n≈2) monoacrylate. The ethylenically unsaturated compound having a carboxyl group can also contain a reaction product of pentaerythritol triacrylate, pentaerythritol trimethacrylate and the like with a dibasic acid anhydride. The ethylenically unsaturated monomer is 2- (meth) acryloyloxyethyl phthalate, 2- (meth) acryloyloxyethyl-2-hydroxyethyl phthalate, linear or branched aliphatic or alicyclic (provided that It may further contain an ethylenically unsaturated compound having no carboxyl group, such as (meth) acrylic acid ester (which may partially have an unsaturated bond in the ring).

  The carboxyl group-containing resin (A2) may contain a compound having a carboxyl group and an ethylenically unsaturated group (hereinafter referred to as “component (A2-2)”). The carboxyl group-containing resin (A2) may contain only the component (A2-2). The component (A2-2) includes, for example, an intermediate that is a reaction product of an epoxy compound (g1) having two or more epoxy groups in one molecule and an ethylenically unsaturated compound (g2), a polyvalent carboxylic acid, and It contains a resin (referred to as a first resin (g)) that is a reaction product with at least one compound (g3) selected from the group of anhydrides. For example, the first resin (g) is obtained by adding the compound (g3) to an intermediate obtained by reacting the epoxy group in the epoxy compound (g1) with the carboxyl group in the ethylenically unsaturated compound (g2). Can be obtained. The epoxy compound (g1) can contain an appropriate epoxy compound such as a cresol novolac epoxy compound, a phenol novolac epoxy compound, or a biphenyl novolac epoxy compound. In particular, the epoxy compound (g1) preferably contains at least one compound selected from the group of biphenyl novolac type epoxy compounds and cresol novolac type epoxy compounds. The epoxy compound (g1) may contain only a biphenyl novolac type epoxy compound or may contain only a cresol novolac type epoxy compound. In this case, since an aromatic ring is contained in the main chain of the epoxy compound (g1), the degree to which the cured product of the photosensitive resin composition is significantly corroded with, for example, an oxidizing agent containing potassium permanganate is reduced. be able to. The epoxy compound (g1) may contain a polymer of the ethylenically unsaturated compound (h). The ethylenically unsaturated compound (h) contains a compound (h1) having an epoxy group such as glycidyl (meth) acrylate, or further has no epoxy group such as 2- (meth) acryloyloxyethyl phthalate. Contains compound (h2). The ethylenically unsaturated compound (g2) preferably contains at least one of acrylic acid and methacrylic acid. The compound (g3) contains one or more compounds selected from the group consisting of polyvalent carboxylic acids such as phthalic acid, tetrahydrophthalic acid, and methyltetrahydrophthalic acid, and anhydrides of these polyvalent carboxylic acids. . In particular, the compound (g3) preferably contains at least one polycarboxylic acid selected from the group of phthalic acid, tetrahydrophthalic acid, and methyltetrahydrophthalic acid.

  The component (A2-2) is a resin (second resin) that is a reaction product of a polymer of an ethylenically unsaturated monomer containing an ethylenically unsaturated compound having a carboxyl group and an ethylenically unsaturated compound having an epoxy group. Of resin (i)). The ethylenically unsaturated monomer may further contain an ethylenically unsaturated compound having no carboxyl group. The second resin (i) can be obtained by reacting an ethylenically unsaturated compound having an epoxy group with a part of the carboxyl group in the polymer. The ethylenically unsaturated monomer may further contain an ethylenically unsaturated compound having no carboxyl group. Examples of the ethylenically unsaturated compound having a carboxyl group include compounds such as acrylic acid, methacrylic acid, ω-carboxy-polycaprolactone (n≈2) monoacrylate, pentaerythritol triacrylate, and pentaerythritol trimethacrylate. Examples of the ethylenically unsaturated compound having no carboxyl group include 2- (meth) acryloyloxyethyl phthalate, 2- (meth) acryloyloxyethyl-2-hydroxyethyl phthalate, linear or branched aliphatic or oil It contains a compound such as a (meth) acrylic acid ester of a cyclic group (however, it may have some unsaturated bonds in the ring). The ethylenically unsaturated compound having an epoxy group preferably contains glycidyl (meth) acrylate.

  The carboxyl group-containing resin (A) can contain only the carboxyl group-containing resin (A1), only the carboxyl group-containing resin (A2), or the carboxyl group-containing resin (A1) and the carboxyl group-containing resin (A2). The carboxyl group-containing resin (A) preferably contains 30% by mass or more of the carboxyl group-containing resin (A1), more preferably 60% by mass or more, and still more preferably 100% by mass. In this case, the heat resistance and insulation reliability of the cured product of the photosensitive resin composition can be particularly improved. Moreover, the tack property of the film | membrane formed from the photosensitive resin composition can fully be suppressed. Furthermore, the developability by the alkaline aqueous solution of the photosensitive resin composition can be ensured.

  The unsaturated compound (B) can impart photocurability to the photosensitive resin composition. The unsaturated compound (B) is, for example, a monofunctional (meth) acrylate such as 2-hydroxyethyl (meth) acrylate; and diethylene glycol di (meth) acrylate, trimethylolpropane di (meth) acrylate, trimethylolpropane tri (meth) Acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol hexa (meth) acrylate, ε-caprolactone modified pentaerythritol hexaacrylate, tricyclodecandi At least one compound selected from the group consisting of polyfunctional (meth) acrylates such as methanol di (meth) acrylate can be contained.

  In particular, the unsaturated compound (B) preferably contains a trifunctional compound, that is, a compound having three unsaturated bonds in one molecule. In this case, the resolution when the film formed from the photosensitive resin composition is exposed and developed is improved, and the developability of the photosensitive resin composition with an alkaline aqueous solution is particularly improved. Trifunctional compounds include, for example, trimethylolpropane tri (meth) acrylate, EO modified trimethylolpropane tri (meth) acrylate, pentaerythritol tri (meth) acrylate, ethoxylated isocyanuric acid tri (meth) acrylate and ε-caprolactone modified It can contain at least one compound selected from the group consisting of tris- (2-acryloxyethyl) isocyanurate and ethoxylated glycerin tri (meth) acrylate.

  It is also preferred that the unsaturated compound (B) contains a phosphorus-containing compound (phosphorus-containing unsaturated compound). In this case, the flame retardancy of the cured product of the photosensitive resin composition is improved. Phosphorus-containing unsaturated compounds include, for example, 2-methacryloyloxyethyl acid phosphate (as specific examples, product number light ester P-1M and light ester P-2M manufactured by Kyoeisha Chemical Co., Ltd.), 2-acryloyloxyethyl acid phosphate (As a specific example, product number light acrylate P-1A manufactured by Kyoeisha Chemical Co., Ltd.), diphenyl-2-methacryloyloxyethyl phosphate (as a specific example, product number MR-260 manufactured by Daihachi Kogyo Co., Ltd.), and Showa Polymer Co., Ltd. HFA series (part number HFA-6003 which is an addition reaction product of dipentaerystol hexaacrylate and HCA (9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide) as a specific example, and HFA-6007, caprolactone One or more compounds selected from the group consisting of product numbers HFA-3003 and HFA-6127, which are addition reaction products of modified dipentaerystol hexaacrylate and HCA) can be contained.

  The unsaturated compound (B) may contain a prepolymer. The prepolymer is at least one selected from the group consisting of, for example, a prepolymer obtained by polymerizing a monomer having an ethylenically unsaturated bond and then adding an ethylenically unsaturated group, and oligo (meth) acrylate prepolymers These compounds can be contained. Oligo (meth) acrylate prepolymers include, for example, epoxy (meth) acrylate, polyester (meth) acrylate, urethane (meth) acrylate, alkyd resin (meth) acrylate, silicone resin (meth) acrylate, and spirane resin (meth) acrylate At least one component selected from the group consisting of:

  The photopolymerization initiator (C) contains, for example, an acyl phosphine oxide photopolymerization initiator (C1). That is, the photosensitive resin composition contains, for example, an acyl phosphine oxide photopolymerization initiator (C1). In this case, when exposing the photosensitive resin composition with ultraviolet rays, high photosensitivity can be imparted to the photosensitive resin composition. Moreover, generation | occurrence | production of the ion migration in the layer containing the hardened | cured material of the photosensitive resin composition is suppressed, and the insulation reliability of the layer containing hardened | cured material further improves.

  Acylphosphine oxide photopolymerization initiator (C1) is, for example, monoacyl such as 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, 2,4,6-trimethylbenzoyl-ethyl-phenyl-phosphinate Phosphine oxide photopolymerization initiator, bis- (2,6-dichlorobenzoyl) phenylphosphine oxide, bis- (2,6-dichlorobenzoyl) -2,5-dimethylphenylphosphine oxide, bis- (2 , 6-Dichlorobenzoyl) -4-propylphenylphosphine oxide, bis- (2,6-dichlorobenzoyl) -1-naphthylphosphine oxide, bis- (2,6-dimethoxybenzoyl) phenylphosphine oxide, bis- (2,6-dimethoxyben Yl) -2,4,4-trimethylpentylphosphine oxide, bis- (2,6-dimethoxybenzoyl) -2,5-dimethylphenylphosphine oxide, bis- (2,4,6-trimethylbenzoyl) phenylphosphine Contains one or more components selected from the group consisting of bisacylphosphine oxide photopolymerization initiators such as fin oxide and (2,5,6-trimethylbenzoyl) -2,4,4-trimethylpentylphosphine oxide it can. In particular, the acylphosphine oxide photopolymerization initiator (C1) preferably contains 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, and the acylphosphine oxide photopolymerization initiator (C1) is 2, It is also preferred to contain only 4,6-trimethylbenzoyl-diphenyl-phosphine oxide.

  The photopolymerization initiator (C) preferably contains a hydroxyketone photopolymerization initiator (C2) in addition to the acylphosphine oxide photopolymerization initiator (C1). That is, it is preferable that the photosensitive resin composition contains a hydroxyketone photopolymerization initiator (C2). In this case, higher photosensitivity can be imparted to the photosensitive resin composition as compared with the case where the hydroxyketone photopolymerization initiator (C2) is not contained. Thereby, when irradiating and hardening an ultraviolet-ray to the coating film formed from the photosensitive resin composition, it becomes possible to fully harden a coating film over the deep part from the surface. Examples of the hydroxyketone photopolymerization initiator (C2) include 1-hydroxy-cyclohexyl-phenyl-ketone, phenylglyoxyc acid methyl ester, and 1- [4- (2-hydroxyethoxy) -phenyl] -2-hydroxy. 2-methyl-1-propan-1-one, 2-hydroxy-1- {4- [4- (2-hydroxy-2-methyl-propionyl) -benzyl] phenyl} -2-methyl-propane-1- On and 2-hydroxy-2-methyl-1-phenyl-propan-1-one.

  The mass ratio of the acylphosphine oxide photopolymerization initiator (C1) and the hydroxyketone photopolymerization initiator (C2) is preferably in the range of 1: 0.01 to 1:10. In this case, the curability in the vicinity of the surface of the coating film formed from the photosensitive resin composition and the curability in the deep portion can be improved in a well-balanced manner. When the photosensitive resin composition contains the organic filler (E1), the organic filler (E1) may cause light scattering in the photosensitive resin composition during exposure. In this case, there may be a problem that good developability cannot be obtained with the photosensitive resin composition. From such a viewpoint, in order to improve the resolution and obtain good developability with the photosensitive resin composition, the acylphosphine oxide photopolymerization initiator (C1) and the hydroxyketone photopolymerization initiator (C2 ) Is particularly preferably in the range of 1: 0.01 to 1: 1.

  It is also preferred that the photopolymerization initiator (C) contains bis (diethylamino) benzophenone (C3). That is, the photosensitive resin composition contains an acyl phosphine oxide photopolymerization initiator (C1) and bis (diethylamino) benzophenone (C3), or an acyl phosphine oxide photopolymerization initiator (C1), a hydroxyketone type. It is also preferable to contain a photopolymerization initiator (C2) and bis (diethylamino) benzophenone (C3). In this case, when developing after partially exposing the coating film formed from the photosensitive resin composition, the resolution is particularly enhanced by suppressing the curing of the unexposed portion. For this reason, it becomes possible to form a very fine pattern with the hardened | cured material of the photosensitive resin composition. In particular, when an interlayer insulating layer of a multilayer printed wiring board is prepared from a photosensitive resin composition and a small-diameter hole for a through hole is provided in the interlayer insulating layer by a photolithography method (see FIG. 1), the small-diameter hole is formed. It becomes possible to form precisely and easily.

  Bis (diethylamino) benzophenone (C3) is preferably in the range of 0.5 to 20% by mass with respect to the acylphosphine oxide photopolymerization initiator (C1). When bis (diethylamino) benzophenone (C3) is 0.5% by mass or more, the resolution is particularly high. Further, when the content of bis (diethylamino) benzophenone (C3) is 20% by mass or less, it is difficult for bis (diethylamino) benzophenone (C3) to inhibit the electrical insulation of the cured product of the photosensitive resin composition. When the photosensitive resin composition contains the organic filler (E1), the organic filler (E1) may cause light scattering in the photosensitive resin composition during exposure. In this case, there may be a problem that good developability cannot be obtained with the photosensitive resin composition. From such a viewpoint, in order to obtain good resolution with the photosensitive resin composition, bis (diethylamino) benzophenone (C3) is 1 to 18 with respect to the acylphosphine oxide photopolymerization initiator (C1). It is particularly preferable to be within the range of mass%.

  The photosensitive resin composition may further contain a known photopolymerization accelerator, sensitizer and the like. For example, the photosensitive resin composition includes benzoin and its alkyl ethers; acetophenones such as acetophenone and benzyldimethyl ketal; anthraquinones such as 2-methylanthraquinone; 2,4-dimethylthioxanthone, 2,4-diethylthioxanthone, 2- Thioxanthones such as isopropylthioxanthone, 4-isopropylthioxanthone and 2,4-diisopropylthioxanthone; benzophenones such as benzophenone and 4-benzoyl-4′-methyldiphenyl sulfide; xanthones such as 2,4-diisopropylxanthone; Α-hydroxyketones such as hydroxy-2-methyl-1-phenyl-propan-1-one; 2-methyl-1- [4- (methylthio) phenyl] -2-morpholino-1-propanone It can contain at least one component selected from the group consisting of compounds containing a nitrogen atom. The photosensitive resin composition is known together with a photopolymerization initiator (C), such as tertiary amines such as p-dimethylbenzoic acid ethyl ester, p-dimethylaminobenzoic acid isoamyl ester, and 2-dimethylaminoethylbenzoate. You may contain a photoinitiator, a sensitizer, etc. If necessary, the photosensitive resin composition may contain at least one of a photopolymerization initiator for visible light exposure and a photopolymerization initiator for near-infrared exposure. The photosensitive resin composition contains a photopolymerization initiator (C) and a coumarin derivative such as 7-diethylamino-4-methylcoumarin that is a sensitizer for laser exposure, a carbocyanine dye system, a xanthene dye system, and the like. May be.

  The epoxy compound (D) can impart thermosetting properties to the photosensitive resin composition. The epoxy compound (D) preferably contains a crystalline epoxy resin. In this case, the developability of the photosensitive resin composition can be improved. Furthermore, since the organic filler (E1) has a carboxyl group as described above, the compatibility of the crystalline epoxy resin is improved by the organic filler (E1), and recrystallization of the crystalline epoxy resin in the photosensitive resin composition is prevented. be able to. The epoxy compound (D) may further contain an amorphous epoxy resin. Here, the “crystalline epoxy resin” is an epoxy resin having a melting point, and the “amorphous epoxy resin” is an epoxy resin having no melting point.

  The crystalline epoxy resin is, for example, 1,3,5-tris (2,3-epoxypropyl) -1,3,5-triazine-2,4,6 (1H, 3H, 5H) -trione, hydroquinone type crystal Epoxy resin (product name YDC-1312 manufactured by Nippon Steel & Sumikin Chemical Co., Ltd.), biphenyl type crystalline epoxy resin (product name YX-4000 manufactured by Mitsubishi Chemical Co., Ltd.), diphenyl ether type crystalline epoxy resin (specific example) As an example, NS Nippon Kayaku Co., Ltd. product number GTR-1800), bisphenolfluorene type crystal Preferably it contains one or more components selected from the group consisting of an epoxy resin (epoxy resin having a structure represented by the formula (7) as a specific example).

  The crystalline epoxy resin preferably has two epoxy groups in one molecule.

  The crystalline epoxy resin preferably has an epoxy equivalent of 150 to 300 g / eq. This epoxy equivalent is the gram weight of a crystalline epoxy resin containing 1 gram equivalent of epoxy groups. The crystalline epoxy resin has a melting point. As melting | fusing point of crystalline epoxy resin, 70-180 degreeC is mentioned, for example.

  In particular, the epoxy compound (D) preferably contains a crystalline epoxy resin having a melting point of 110 ° C. or lower. In this case, the developability of the photosensitive resin composition with an alkaline aqueous solution is particularly improved. Crystalline epoxy resins having a melting point of 110 ° C. or less include, for example, biphenyl type epoxy resin (specifically, product number YX-4000 manufactured by Mitsubishi Chemical Corporation), biphenyl ether type epoxy resin (specifically, product number YSLV manufactured by Nippon Steel & Sumikin Chemical Co., Ltd.) -80DE), and a bisphenol type epoxy resin (as a specific example, product number YSLV-80XY manufactured by Nippon Steel & Sumikin Chemical), a bisphenol fluorene type crystalline epoxy resin (specifically, an epoxy resin having a structure represented by formula (7)) It can contain at least one component selected from More specifically, the crystalline epoxy resin is selected from the group consisting of a biphenyl type epoxy resin (product number YX-4000 manufactured by Mitsubishi Chemical Corporation) and a bisphenol type epoxy resin (product number YSLV-80XY manufactured by Nippon Steel & Sumikin Chemical). At least one component.

  The amorphous epoxy resin is, for example, a phenol novolac type epoxy resin (specifically, product number EPICLON N-775 manufactured by DIC Corporation), or a cresol novolac type epoxy resin (specific example, product number EPICLON N-695 manufactured by DIC Corporation). Bisphenol A novolac type epoxy resin (specifically, product number EPICLON N-865 manufactured by DIC Corporation), bisphenol A type epoxy resin (specifically, product number jER1001 manufactured by Mitsubishi Chemical Corporation), bisphenol F type epoxy resin (specific example) As product number jER4004P manufactured by Mitsubishi Chemical Corporation), bisphenol S type epoxy resin (specifically, product number EPICLON EXA-1514 manufactured by DIC Corporation), bisphenol AD type epoxy resin, biphenyl novolak type Poxy resin (part number NC-3000 manufactured by Nippon Kayaku Co., Ltd.), hydrogenated bisphenol A type epoxy resin (part number ST-4000D manufactured by Nippon Steel & Sumikin Chemical Co., Ltd.), naphthalene type epoxy resin (particular example) DIC Corporation product numbers EPICLON HP-4032, EPICLON HP-4700, EPICLON HP-4770), tertiary butyl catechol type epoxy resin (specifically, product number EPICLON HP-820 manufactured by DIC Corporation), dicyclopentadiene type Epoxy resin (part number EPICLON HP-7200 manufactured by DIC as a specific example), adamantane type epoxy resin (part number ADAMANATE X-E-201 manufactured by Idemitsu Kosan Co., Ltd.), special bifunctional type epoxy resin (specific example , Mitsubishi Chemical Corporation part numbers YL7175-500 and YL7175-1000; DIC Corporation part numbers EPICLON TSR-960, EPICLON TER-601, EPICLON TSR-250-80BX, EPICLON 1650-75MPX, EPICLON EXA-4850, EPICLON EXA-4816, EPICLON EXA-4822, and EPICLON EXA-9726; Nippon Steel & Sumikin Chemical Co., Ltd. product number YSLV-120TE), rubber core-shell polymer modified bisphenol A type epoxy resin (specifically, product number MX manufactured by Kaneka Corporation) 156), and a rubbery core-shell polymer-modified bisphenol F type epoxy resin (as a specific example, product number MX-136 manufactured by Kaneka Corporation) It is preferable to contain one or more components selected from the above.

  The epoxy compound (D) may contain a phosphorus-containing epoxy resin. In this case, the flame retardancy of the cured product of the photosensitive resin composition is improved. The phosphorus-containing epoxy resin may be contained in the crystalline epoxy resin or may be contained in the amorphous epoxy resin. Examples of phosphorus-containing epoxy resins include phosphoric acid-modified bisphenol F-type epoxy resins (specific examples of product numbers EPICLON EXA-9726 and EPICLON EXA-9710 manufactured by DIC Corporation), and product number Epototo FX-305 manufactured by Nippon Steel & Sumikin Chemical Co., Ltd. Is mentioned.

  The organic filler (E) can impart thixotropy to the photosensitive resin composition. The organic filler (E) includes an organic filler (E1). The organic filler (E1) has a carboxyl group. Among the carboxyl groups, some of the carboxyl groups are preferably exposed on the surface of the organic filler (E1).

  The organic filler (E1) has high compatibility in the photosensitive resin composition and can impart stronger thixotropy to the photosensitive resin composition. When the photosensitive resin composition contains the organic filler (E1) having a carboxyl group, the developability of the photosensitive resin composition can be improved. Moreover, the carboxyl group of an organic filler (E1) can react with the epoxy compound (for example, epoxy compound (D)) in the photosensitive resin composition at the time of thermosetting. Thereby, the hardened | cured material after thermosetting can contain the organic filler (E1) disperse | distributed uniformly in the inside. Furthermore, the unreacted carboxyl group of the organic filler (E1) can be modified at the stage of roughening the surface of the cured product. That is, among the organic filler (E1) contained in the cured product, the organic filler (E1) located near the surface of the cured product is easily deteriorated at the stage of roughening the surface of the cured product. The organic filler (E1) thus altered is easily removed from the cured product when a rough surface is imparted to the cured product. Thereby, a rough surface can be provided to the surface of the cured product to improve the adhesion between the cured product and the plating layer.

  Furthermore, the non-uniformity of the coating film resulting from the fluidity | liquidity of the photosensitive resin composition can be reduced because the photosensitive resin composition contains the organic filler (E1). Thereby, the film thickness of the layer formed with the photosensitive resin composition can be easily made uniform. In this case, the photosensitive resin composition may not contain a rheology control agent. Examples of the rheology control agent include urea-modified medium polarity polyamides (product numbers BYK-430 and BYK-431 manufactured by Big Chemie Japan Co., Ltd.) and polyhydroxycarboxylic acid amides (product number BYK-405 manufactured by Big Chemie Japan Co., Ltd.). ), Modified urea (product numbers BYK-410, BYK-411, BYK-420 manufactured by Big Chemie Japan Co., Ltd.), polymer urea derivatives (product number BYK-415 manufactured by Big Chemie Japan Co., Ltd.), urea modified urethane (Big Chemie Japan) Product number BYK-425) manufactured by Japan Co., Ltd., polyurethane (product number BYK-428 manufactured by Big Chemie Japan Co., Ltd.), castor oil wax, polyethylene wax, polyamide wax, bentonite, silica, silica gel, kaolin, Rate, and the like.

  The carboxyl group of the organic filler (E1) is formed as a side chain in the product by polymerizing or crosslinking a carboxylic acid monomer such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, fumaric acid, itaconic acid, etc. Is done. The carboxylic acid monomer has a carboxyl group and a polymerizable unsaturated double bond. The organic filler (E1) improves the stability (particularly storage stability) of the photosensitive resin composition in order to enhance the thixotropy of the photosensitive resin composition. Furthermore, since the organic filler (E1) has a carboxyl group, it improves the developability of the cured product and improves the compatibility of the crystalline epoxy resin to prevent crystallization in the photosensitive resin composition. it can. The carboxyl group content of the organic filler (E1) is not particularly limited, but the acid value of the organic filler (E1) is preferably 1 to 60 mgKOH / g by acid-base titration. If the acid value is less than 1 mgKOH / g, the stability of the photosensitive resin composition and the developability of the cured product may be reduced. If the acid value is larger than 60 mgKOH / g, the moisture resistance reliability of the cured product may be lowered. The acid value of the organic filler (E1) is more preferably 3 to 40 mgKOH / g.

  The organic filler (E1) also preferably has a hydroxyl group. Of these hydroxyl groups, some hydroxyl groups are preferably exposed on the surface of the organic filler (E1). Thus, the dispersibility of the organic filler (E1) in the photosensitive resin composition further improves because the organic filler (E1) has a hydroxyl group.

The organic filler (E1) preferably has an average primary particle size of 1 μm or less. When the average primary particle diameter of the organic filler (E1) is 1 μm or less, the roughness of the rough surface formed on the cured product can be reduced. Thereby, as the surface area of the cured product increases, the anchor effect increases and the adhesion between the rough surface and the plating layer can be improved. The lower limit of the average primary particle diameter of the organic filler (E1) is not particularly limited, but is preferably 0.001 μm or more, for example. The average primary particle size by a laser diffraction particle size distribution measuring device, is measured as D _50. The average primary particle diameter of the organic filler (E1) is more preferably 0.4 μm or less, and further preferably 0.1 μm or less. In this case, the roughness of the rough surface formed in the cured product can be made particularly fine. In addition, scattering during exposure can be suppressed in the photosensitive resin composition, whereby the resolution of the photosensitive resin composition can be further improved.

The organic filler (E1) is preferably dispersed with a maximum particle size of less than 1.0 μm, more preferably less than 0.5 μm, in the photosensitive resin composition. Maximum particle diameter, by laser diffraction type particle size distribution measuring device, is measured as D _50. Alternatively, the maximum particle size is measured by observing the cured product with a transmission electron microscope (TEM). The organic filler (E1) may aggregate in the photosensitive resin composition (for example, can form secondary particles). In this case, the maximum particle diameter means the size of the particles after aggregation. When the maximum particle size of the organic filler (E1) in the dispersed state is in the above range, the roughness of the rough surface formed on the cured product can be further reduced. In addition, scattering during exposure is suppressed in the photosensitive resin composition, thereby further improving the resolution of the photosensitive resin composition. When particle aggregation occurs, the maximum particle size is usually larger than the average primary particle size.

  The organic filler (E1) preferably contains a rubber component. Moreover, it is preferable that an organic filler (E1) contains only a rubber component. The rubber component can impart flexibility to the cured product of the photosensitive resin composition. The rubber component can be composed of a resin. The rubber component preferably contains at least one polymer selected from crosslinked acrylic rubber, crosslinked NBR, crosslinked MBS, and crosslinked SBR. In this case, the rubber component can impart excellent flexibility to the cured product of the photosensitive resin composition. Furthermore, a more appropriate rough surface can be imparted to the surface of the cured product. Here, the rubber component includes a crosslinked structure formed when the monomers constituting the polymer are copolymerized. NBR is generally a copolymer of butadiene and acrylonitrile, and is classified as a nitrile rubber. MBS is generally a copolymer composed of three components of methyl methacrylate, butadiene, and styrene, and is classified as a butadiene rubber. SBR is generally a copolymer of styrene and butadiene, and is classified as styrene rubber. Specific examples of the organic filler (E1) include product number XER-91-MEK manufactured by JSR Corporation, product number XER-32-MEK manufactured by JSR Corporation, product number XSK-500 manufactured by JSR Corporation, and the like. Among these organic fillers (E1), XER-91-MEK is a crosslinked rubber (NBR) having a carboxyl group having an average primary particle size of 0.07 μm, and a methyl ethyl ketone dispersion having a content of 15% by weight of the crosslinked rubber. With an acid value of 10.0 mg KOH / g. XER-32-MEK is a dispersion in which a carboxyl group-modified hydrogenated nitrile rubber polymer (linear particles) is dispersed in methyl ethyl ketone at a content of 17% by weight with respect to the total amount of the dispersion. XSK-500 is a crosslinked rubber (SBR) having an average primary particle size of 0.07 μm and having a carboxyl group and a hydroxyl group, and is provided as a methyl ethyl ketone dispersion having a content of the crosslinked rubber of 15% by weight. Thus, an organic filler (E1) may be mix | blended with the photosensitive resin composition with a dispersion liquid. That is, a rubber component can be mix | blended with the photosensitive resin composition with a dispersion liquid. Further, as a specific example of the organic filler (E1), in addition to the above, product number XER-92 manufactured by JSR Corporation may be mentioned.

  The organic filler (E1) may contain a particle component other than the rubber component. In this case, the organic filler (E1) can contain at least one particle component selected from the group consisting of acrylic resin fine particles having a carboxyl group and cellulose fine particles having a carboxyl group. The acrylic resin fine particles having a carboxyl group can contain at least one particle component selected from the group consisting of non-crosslinked styrene / acrylic resin fine particles and crosslinked styrene / acrylic resin fine particles. As a specific example of the non-crosslinked styrene / acrylic resin fine particles, product number FS-201 (average primary particle size 0.5 μm) manufactured by Nippon Paint Industrial Coatings Co., Ltd. may be mentioned. As specific examples of crosslinked styrene / acrylic resin fine particles, product number MG-351 (average primary particle size: 1.0 μm) and product number BGK-001 (average primary particle size: 1.0 μm) manufactured by Nippon Paint Industrial Coatings Co., Ltd. Is mentioned. The organic filler (E1) may contain a particle component other than the particle component selected from the rubber component, the acrylic resin fine particles, and the cellulose fine particles. In this case, the organic filler (E1) can contain a particle component having a carboxyl group. That is, the particle component having a carboxyl group may be different from the particle component selected from the rubber component, the acrylic resin fine particles, and the cellulose fine particles.

  The organic filler (E) may further contain an organic filler other than the organic filler (E1). Organic fillers other than the said organic filler (E1) do not need to have a carboxyl group. The organic filler other than the organic filler (E1) may have an average primary particle size larger than 1 μm. However, from the viewpoint of imparting a rough surface to the cured product and improving the resolution of the photosensitive resin composition, the photosensitive resin composition may not include an organic filler other than the organic filler (E1). .

  The organic filler (E) may contain only the organic filler (E1) or an organic filler other than the organic filler (E1) and the organic filler (E1). The organic filler (E) preferably contains 30% by mass or more, more preferably 50% by mass or more, and still more preferably 100% by mass of the organic filler (E1). In this case, it becomes easier to give a rough surface to the cured product of the photosensitive resin composition. Thereby, the adhesiveness of hardened | cured material and a plating layer can further be improved.

  As described above, the melamine compound (F) is at least one compound selected from the group of melamine and melamine derivatives. Thereby, the grade which remarkably corrodes the hardened | cured material of the photosensitive resin composition with the oxidizing agent containing potassium permanganate, for example can be reduced. That is, when the photosensitive resin composition contains the melamine compound (F), the thickness of the layer containing the cured product when the surface of the cured product of the photosensitive resin composition is roughened in the previous step of plating treatment. Can be made difficult to thin. Thus, by providing a rough surface to the cured product, adhesion between the cured product of the photosensitive resin composition and a plating layer made of copper, gold, or the like can be improved.

  When the photosensitive resin composition contains both the melamine compound (F) and the organic filler (E), an appropriate rough surface can be imparted to the cured product of the photosensitive resin composition, and the cured product and plating can be provided. Adhesion with the layer can be improved. When a rough surface is imparted to the cured product in the previous step of the plating treatment, it is possible to make it difficult to excessively reduce the thickness of the layer formed of the photosensitive resin composition.

In this embodiment, a melamine compound (F) may contain only a melamine, may contain only a melamine derivative, and may contain a melamine and a melamine derivative. Melamine is 2,4,6-triamino-1,3,5-triazine and is generally available from commercially available compounds. The melamine derivative may be a compound having one triazine ring and an amino group in one molecule. Examples of melamine derivatives include guanamine; acetoguanamine; benzoguanamine; 2,4-diamino-6-methacryloyloxyethyl-S-triazine, 2-vinyl-4,6-diamino-S-triazine, 2-vinyl-4,6. -S-triazine derivatives such as diamino-S-triazine isocyanuric acid adduct, 2,4-diamino-6-methacryloyloxyethyl-S-triazine isocyanuric acid adduct; and melamine such as melamine-tetrahydrophthalate A reaction product with an acid anhydride is mentioned. Specific examples of the melamine derivative include Shikoku Kasei Kogyo Co., Ltd. product name VD-1, product name VD-2, and product name VD-3. The melamine derivative is preferably a compound having one triazine ring and two or more amino groups in one molecule. Of the two or more amino groups, at least one is a substituent that does not contain a —NH ₂ group. That is, the melamine derivative does not contain melamine. In such a case, the melamine derivative dispersed in the photosensitive resin composition is included in, for example, the conductive wiring of the plating layer or the core material and arranged with the metal element located on the contact surface with the photosensitive resin composition. Join. For this reason, the adhesiveness of the photosensitive resin composition can be improved. Examples of the metal element include gold, silver, copper, and nickel.

The melamine compound (F) may be soluble in the photosensitive resin composition. Alternatively, when the melamine compound (F) is hardly soluble in the photosensitive resin composition, the melamine compound (F) having an average particle diameter of 20 μm or less, preferably 15 μm or less is dispersed in the photosensitive resin composition. It is preferable. When the melamine compound (F) is uniformly dispersed in the photosensitive resin composition, the melamine compound (F) is more easily coordinated with the metal element. Thereby, the adhesiveness of the photosensitive resin composition can further be improved. Although the minimum of the average particle diameter of a melamine compound (F) is not specifically limited, It can be 0.01 micrometer or more. The average particle size of the melamine compound (F) by a laser diffraction particle size distribution measuring apparatus in a state dispersed melamine compound (F) in the photosensitive resin composition of the uncured, measured as D _50.

  The photosensitive resin composition can contain a silane coupling agent. In this case, the dispersibility of the organic filler (E) can be improved. Furthermore, the resolution of the photosensitive resin composition can be improved.

The silane coupling agent contains, for example, a silicon atom and ₂ to 4 hydrolyzable groups selected from the group of —OCH ₃ group, —OC ₂ H ₅ group, and —OCOCH ₃ group It is. Silane coupling agents may contain reactive groups such as amino groups, epoxy groups, vinyl (allyl) groups, methacryl groups, mercapto groups, isocyanate groups, sulfide groups, or methyl groups in addition to hydrolyzable groups. Good.

  Examples of the silane coupling agent include 3- (2-aminoethylamino) propyldimethoxymethylsilane, 3- (2-aminoethylamino) propyltriethoxysilane, and 3- (2-aminoethylamino) propyltrimethoxysilane. Amino compounds such as 3-aminopropyldiethoxymethylsilane, 3-aminopropyltriethoxysilane, 3-aminopropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, Epoxys such as 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3-glycidyloxypropyl (dimethoxy) methylsilane, diethoxy (3-glycidyloxypropyl) methylsilane, 3-acryloxypropyltrimethoxysilane (Meth) acrylates such as 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropyltriethoxysilane, 3-methacryloxypropylmethyldimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, vinyltrimethoxysilane, vinyl Vinyl compounds such as triethoxysilane, p-styryltrimethoxysilane, diethoxymethylvinylsilane, vinyltris (2-methoxyethoxy) silane, allyl compounds such as allyltriethoxysilane, allyltrimethoxysilane, p-styryltrimethoxysilane, etc. Styryl compounds, isocyanates such as 3-isocyanatopropyltrimethoxysilane, 3-isocyanatopropyltriethoxysilane, 3-ureidopropyltrimethoxysilane, Ureides such as idpropyltriethoxysilane, mercapto compounds such as (3-mercaptopropyl) triethoxysilane, (3-mercaptopropyl) trimethoxysilane, sulfides such as bis (triethoxysilylpropyl) tetrasulfide, orthosilicate Examples include tetraethyl acid and methyltrimethoxysilane.

  In the present embodiment, for example, the photosensitive resin composition may contain an inorganic filler. In this case, the curing shrinkage of the film formed from the photosensitive resin composition is reduced. The inorganic filler can contain, for example, one or more materials selected from the group consisting of barium sulfate, crystalline silica, nano silica, carbon nanotubes, talc, bentonite, aluminum hydroxide, magnesium hydroxide, and titanium oxide. You may whiten the photosensitive resin composition and its hardened | cured material by making an inorganic filler contain white materials, such as a titanium oxide and a zinc oxide. Although the ratio of the inorganic filler in the photosensitive resin composition is appropriately set, it is preferably in the range of 0 to 300% by mass with respect to the carboxyl group-containing resin (A).

  The photosensitive resin composition according to the present embodiment may contain an organic solvent. The organic solvent is used for the purpose of liquefaction or varnishing of the photosensitive resin composition, viscosity adjustment, application property adjustment, film formation property adjustment, and the like.

  Organic solvents include, for example, linear, branched, secondary or polyhydric alcohols such as ethanol, propyl alcohol, isopropyl alcohol, hexanol and ethylene glycol; ketones such as methyl ethyl ketone and cyclohexanone; aromatic hydrocarbons such as toluene and xylene Petroleum aromatic mixed solvents such as Swazol series (manufactured by Maruzen Petrochemical Co., Ltd.) and Solvesso series (manufactured by Exxon Chemical Co.); cellosolves such as cellosolve and butylcellosolve; Tolls; propylene glycol alkyl ethers such as propylene glycol methyl ether; polypropylene glycol alkyl ethers such as dipropylene glycol methyl ether; ethyl acetate, butyl acetate, cellosolve acetate, carb It can contain, as well as one or more compounds selected from the group consisting of dialkyl glycol ethers; Lumpur acid esters such as acetate.

  The amount of the component in the photosensitive resin composition is appropriately adjusted so that the photosensitive resin composition has photocurability and can be developed with an alkaline solution.

  The carboxyl group-containing resin (A) is preferably in the range of 5 to 85% by mass, more preferably in the range of 10 to 75% by mass, and more preferably in the range of 30 to 60% with respect to the solid content of the photosensitive resin composition. It is more preferable if it is within the range of mass%.

  The unsaturated compound (B) is preferably in the range of 1 to 50% by mass, more preferably in the range of 10 to 45% by mass with respect to the carboxyl group-containing resin (A), and more preferably 21 to 40% by mass. If it is in the range, it is more preferable.

  The photopolymerization initiator (C) is preferably in the range of 0.1 to 30% by mass and more preferably in the range of 1 to 25% by mass with respect to the carboxyl group-containing resin (A).

  Regarding the amount of the epoxy compound (D), the total equivalent of the epoxy groups contained in the epoxy compound (D) is 0.7 to 2.5 with respect to 1 equivalent of the carboxyl group contained in the carboxyl group-containing resin (A). Is preferably in the range of 0.7 to 2.3, more preferably in the range of 0.7 to 2.0. Moreover, it is preferable that the sum total of the equivalent of the epoxy group contained in crystalline epoxy resin exists in the range of 0.1-2.0 with respect to 1 equivalent of carboxyl groups contained in carboxyl group-containing resin (A), A range of 0.2 to 1.9 is more preferable, and a range of 0.3 to 1.5 is more preferable.

  The content of the organic filler (E) is preferably in the range of 1 to 40 parts by mass when the content of the carboxyl group-containing resin (A) is 100 parts by mass. When the content of the organic filler (E) is within this range, the surface of the cured product of the photosensitive resin composition can be appropriately roughened, and thereby the adhesion between the rough surface of the cured product and the plating layer can be achieved. Can be improved. The content of the organic filler (E) is more preferably in the range of 5 to 20 parts by mass, when the content of the carboxyl group-containing resin (A) is 100 parts by mass, More preferably within the range. Moreover, it is preferable that content of an organic filler (E1) exists in the range of 1-40 mass parts, when content of carboxyl group-containing resin (A) is 100 mass parts. When the content of the organic filler (E1) is within this range, the surface of the cured product of the photosensitive resin composition can be more appropriately roughened. The content of the organic filler (E1) is more preferably in the range of 5 to 20 parts by mass, when the content of the carboxyl group-containing resin (A) is 100 parts by mass, and is 10 to 17 parts by mass. More preferably it is. The content of the rubber component is preferably in the range of 1 to 40 parts by mass, and in the range of 5 to 20 parts by mass, when the content of the carboxyl group-containing resin (A) is 100 parts by mass. More preferred is 10 to 17 parts by mass.

  The melamine compound (F) is preferably in the range of 0.1 to 10% by mass and more preferably in the range of 0.5 to 5% by mass with respect to the carboxyl group-containing resin (A).

  When the photosensitive resin composition contains a silane coupling agent, the content of the silane coupling agent ranges from 0.01 to 7 parts by mass when the content of the organic filler (E) is 100 parts by mass. It is preferable to be within. When the content of the silane coupling agent is within this range, aggregation of the organic filler (E) in the photosensitive resin composition is prevented, and dispersibility is improved. The content of the silane coupling agent is more preferably in the range of 0.05 to 5 parts by mass when the content of the organic filler (E) is 100 parts by mass. Moreover, it is preferable that content of a silane coupling agent exists in the range of 0.01-7 mass parts, when content of an organic filler (E1) is 100 mass parts. When the content of the silane coupling agent falls within this range, aggregation of the organic filler (E1) in the photosensitive resin composition is efficiently prevented, and dispersibility is effectively improved. The content of the silane coupling agent is more preferably in the range of 0.05 to 5 parts by mass when the content of the organic filler (E1) is 100 parts by mass.

  When the photosensitive resin composition contains an organic solvent, the amount of the organic solvent is determined so that the organic solvent is volatilized quickly when the coating film formed from the photosensitive resin composition is dried, that is, the organic solvent is dried. It is preferable to adjust so as not to remain in the film. In particular, the organic solvent is preferably in the range of 0 to 99.5% by mass and more preferably in the range of 15 to 60% by mass with respect to the entire photosensitive resin composition. In addition, since the suitable ratio of an organic solvent changes with application methods etc., it is preferable that a ratio is suitably adjusted according to the application method.

  In addition, solid content is a total amount of all components remove | excluding volatile components, such as a solvent, from the photosensitive resin composition.

  Unless it deviates from the main point of this invention, the photosensitive resin composition may further contain components other than the said component.

  Photosensitive resin composition comprising tolylene diisocyanate, morpholine diisocyanate, isophorone diisocyanate and hexamethylene diisocyanate blocked isocyanates blocked with caprolactam, oxime, malonic acid ester, etc .; melamine resin, n-butylated melamine resin , Amino resins such as isobutylated melamine resin, butylated urea resin, butylated melamine urea cocondensation resin, benzoguanamine cocondensation resin; various other thermosetting resins; ultraviolet curable epoxy (meth) acrylate; bisphenol A type , Resins obtained by adding (meth) acrylic acid to phenolic novolac type, cresol novolac type, alicyclic type epoxy resins; and diallyl phthalate resin, phenoxy resin, urethane resin, fluorine resin, etc. It may contain one or more resins that are selected from the group consisting of a polymer compound.

  The photosensitive resin composition may contain a curing agent for curing the epoxy compound (D). Examples of the curing agent include imidazole, 2-methylimidazole, 2-ethylimidazole, 2-ethyl-4-methylimidazole, 2-phenylimidazole, 4-phenylimidazole, 1-cyanoethyl-2-phenylimidazole, 1- (2 Imidazole derivatives such as -cyanoethyl) -2-ethyl-4-methylimidazole; dicyandiamide, benzyldimethylamine, 4- (dimethylamino) -N, N-dimethylbenzylamine, 4-methoxy-N, N-dimethylbenzylamine, Amine compounds such as 4-methyl-N, N-dimethylbenzylamine; hydrazine compounds such as adipic hydrazide and sebacic acid hydrazide; phosphorus compounds such as triphenylphosphine; acid anhydrides; phenols; mercaptans; And It may contain one or more components selected from the group consisting um salt. Examples of commercially available products of these components include 2MZ-A, 2MZ-OK, 2PHZ, 2P4BHZ, 2P4MHZ (both trade names of imidazole compounds) manufactured by Shikoku Kasei Co., Ltd., U-CAT3503N, U manufactured by San Apro Co., Ltd. -CAT3502T (all are trade names of blocked isocyanate compounds of dimethylamine), DBU, DBN, U-CATSA102, U-CAT5002 (all are bicyclic amidine compounds and salts thereof).

  The photosensitive resin composition includes a curing accelerator; a colorant; a copolymer such as silicone and acrylate; an adhesiveness imparting agent such as a leveling agent; a thixotropic agent; a polymerization inhibitor; an antihalation agent; a rheology control agent; One or more components selected from the group consisting of an antifoaming agent, an antioxidant, a surfactant, a pigment, and a polymer dispersant may be contained. In addition, the photosensitive resin composition does not need to contain a pigment.

  The content of the amine compound in the photosensitive resin composition is preferably as small as possible. In this case, the electrical insulation of the layer made of a cured product of the photosensitive resin composition is not easily impaired. In particular, the amine compound is preferably 6% by mass or less, more preferably 4% by mass or less, based on the carboxyl group-containing resin (A).

  The raw material of the photosensitive resin composition as described above is blended, and the photosensitive resin composition can be prepared by kneading by a known kneading method using, for example, a three roll, ball mill, sand mill or the like. In the case where the raw material of the photosensitive resin composition contains a liquid component, a low viscosity component, etc., the part of the raw material excluding the liquid component, the low viscosity component, etc. is first kneaded, and the resulting mixture is The photosensitive resin composition may be prepared by adding and mixing a liquid component, a component having a low viscosity, and the like.

  In consideration of storage stability and the like, the first agent may be prepared by mixing a part of the components of the photosensitive resin composition, and the second agent may be prepared by mixing the rest of the components. That is, the photosensitive resin composition may include a first agent and a second agent. In this case, for example, the first agent is prepared by previously mixing and dispersing the unsaturated compound (B), a part of the organic solvent, and the thermosetting component among the components of the photosensitive resin composition. You may prepare a 2nd agent by mixing and disperse | distributing the remainder among the components of a composition. In this case, it is possible to prepare a mixed solution by mixing the necessary amount of the first agent and the second agent in a timely manner and curing the mixed solution to obtain a cured product.

  The photosensitive resin composition according to this embodiment is suitable as an electrically insulating material for a printed wiring board. In particular, the photosensitive resin composition is suitable for forming an electrically insulating layer such as a solder resist layer, a plating resist layer, an etching resist layer, and an interlayer insulating layer.

  When the photosensitive resin composition according to the present embodiment is formed into a film having a thickness of 25 μm, it is preferable that the film can be developed with an aqueous sodium carbonate solution. In this case, since a sufficiently thick electrically insulating layer can be produced from the photosensitive resin composition by photolithography, the photosensitive resin composition is used as an interlayer insulating layer or solder resist in a printed wiring board. Widely applicable for producing layers and the like. Of course, it is also possible to produce an electrically insulating layer having a thickness of less than 25 μm from the photosensitive resin composition.

It can be confirmed by the following method that the film can be developed with an aqueous sodium carbonate solution. A wet paint film is formed by applying the photosensitive resin composition on a suitable substrate, and this wet paint film is heated at 80 ° C. for 40 minutes to form a film having a thickness of 25 μm. In a state where a negative mask having an exposed portion that transmits ultraviolet rays and a non-exposed portion that blocks ultraviolet rays is directly applied to the coating, the coating is irradiated with ultraviolet rays through the negative mask under the condition of 500 mJ / cm ² . A 1% Na ₂ CO ₃ aqueous solution at 30 ° C. is sprayed for 90 seconds at an injection pressure of 0.2 MPa on the film after exposure, and then pure water is sprayed for 90 seconds at an injection pressure of 0.2 MPa. As a result of observing the film after this treatment, it can be determined that development is possible when a portion corresponding to the non-exposed part of the film is removed and no residue is observed.

  Below, an example of the method of manufacturing a printed wiring board provided with the interlayer insulation layer formed from the photosensitive resin composition by this embodiment is demonstrated with reference to FIG. 1A to FIG. 1E. In this method, a through hole is formed in the interlayer insulating layer by photolithography.

  First, the core material 1 is prepared as shown in FIG. 1A. The core material 1 includes, for example, at least one insulating layer 2 and at least one conductor wiring 3. The conductor wiring 3 provided on one surface of the core material 1 is hereinafter referred to as a first conductor wiring 3. As shown to FIG. 1B, the film | membrane 4 is formed from the photosensitive resin composition on the surface in which the 1st conductor wiring 3 of the core material 1 is provided. Examples of the method for forming the film 4 include a coating method and a dry film method.

  In the coating method, for example, a photosensitive resin composition is coated on the core material 1 to form a wet coating film. The method for applying the photosensitive resin composition is selected from the group consisting of known methods such as dipping, spraying, spin coating, roll coating, curtain coating, and screen printing. Subsequently, in order to volatilize the organic solvent in the photosensitive resin composition, the wet coating film is dried at a temperature in the range of 60 to 120 ° C., for example, and the coating film 4 can be obtained.

  In the dry film method, first, a photosensitive resin composition is applied on an appropriate support made of polyester or the like, and then dried to form a dry film containing the photosensitive resin composition on the support. Thereby, the dry film with a support provided with a dry film and the support body which supports a dry film is obtained. In this dry film with a support, the dry film is laminated on the core material 1, then pressure is applied to the dry film and the core material 1, and then the support is peeled off from the dry film, whereby the dry film is cored on the support. Transfer onto material 1. Thereby, the coating 4 made of a dry film is provided on the core material 1.

  The coating 4 is exposed to light and partially cured as shown in FIG. 1C. For this purpose, for example, a negative mask is applied to the film 4 and then the film 4 is irradiated with ultraviolet rays through the negative mask. The negative mask includes an exposure part that transmits ultraviolet rays and a non-exposure part that blocks ultraviolet rays. The negative mask is a photo tool such as a mask film or a dry plate. The ultraviolet light source is selected from the group consisting of chemical lamps, low-pressure mercury lamps, medium-pressure mercury lamps, high-pressure mercury lamps, ultra-high-pressure mercury lamps, xenon lamps, and metal halide lamps, for example.

  As an exposure method, a method other than a method using a negative mask may be employed. For example, the film may be exposed by a direct drawing method in which ultraviolet rays emitted from a light source are irradiated only on a portion to be exposed on the film 4. The light source applied to the direct drawing method is, for example, a high-pressure mercury lamp, an ultrahigh-pressure mercury lamp, a metal halide lamp, g-line (436 nm), h-line (405 nm), i-line (365 nm), and g-line, h-line, and i-line. It is selected from the group consisting of two or more kinds of combinations.

  In the dry film method, after the dry film in the dry film with the support is stacked on the core material 1, the support 4 is transmitted through the support 4 without irradiating the film 4 made of the dry film without peeling off the support. Then, the coating 4 may be exposed to light, and then the support may be peeled off from the coating 4 before the development treatment.

  Subsequently, the coating 4 is developed to remove the unexposed portion 5 of the coating 4 shown in FIG. 1C, whereby the hole 6 is formed at the position where the through hole 10 is formed as shown in FIG. 1D. Is provided. In the development process, an appropriate developer according to the composition of the photosensitive resin composition can be used. The developer is, for example, an alkaline aqueous solution containing at least one of an alkali metal salt and an alkali metal hydroxide, or an organic amine. More specifically, the alkaline aqueous solution is, for example, sodium carbonate, potassium carbonate, ammonium carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate, ammonium hydrogen carbonate, sodium hydroxide, potassium hydroxide, ammonium hydroxide, tetramethyl ammonium hydroxide and water. It contains at least one component selected from the group consisting of lithium oxide. The solvent in the alkaline aqueous solution may be water alone or a mixture of water and a hydrophilic organic solvent such as lower alcohols. The organic amine contains, for example, at least one component selected from the group consisting of monoethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine and triisopropanolamine.

  The developer is preferably an alkaline aqueous solution containing at least one of an alkali metal salt and an alkali metal hydroxide, and particularly preferably an aqueous sodium carbonate solution. In this case, it is possible to improve the work environment and reduce the burden of waste disposal.

  Subsequently, the coating 4 is thermally cured by heating. The heating conditions are, for example, within a heating temperature range of 120 to 200 ° C. and within a heating time range of 30 to 120 minutes. When the film 4 is thermally cured in this manner, the performance of the interlayer insulating layer 7 such as strength, hardness, and chemical resistance is improved.

  If necessary, the coating 4 may be further irradiated with ultraviolet rays before or after heating. In this case, photocuring of the film 4 can be further advanced.

  As described above, the interlayer insulating layer 7 made of a cured product of the photosensitive resin composition is provided on the core material 1. The second conductor wiring 8 and the hole plating 9 can be provided on the interlayer insulating layer 7 by a known method such as an additive method. As a result, as shown in FIG. 1E, the first conductor wiring 3, the second conductor wiring 8, the interlayer insulating layer 7 interposed between the first conductor wiring 3 and the second conductor wiring 8, and the first conductor wiring A printed wiring board 11 having a through hole 10 for electrically connecting the first conductor wiring 3 and the second conductor wiring 8 is obtained. In FIG. 1E, the hole plating 9 has a cylindrical shape that covers the inner surface of the hole 6, but the entire inner side of the hole 6 may be filled with the hole plating 9.

  Further, before the hole plating 9 as shown in FIG. 1E is provided, the entire inner surface of the hole 6 and a part of the outer surface of the interlayer insulating layer 7 can be roughened. In this manner, the adhesion between the core material 1 and the hole plating 9 can be improved by roughening a part of the outer surface of the interlayer insulating layer 7 and the inner side surface of the hole 6.

  In roughening a part of the outer surface of the interlayer insulating layer 7 and the entire inner surface of the hole 6, the same procedure as a general desmear process using an oxidizing agent can be performed. For example, an oxidizing agent is brought into contact with the outer surface of the interlayer insulating layer 7 to give a rough surface to the interlayer insulating layer 7. However, the present invention is not limited to this, and a method of imparting a rough surface to a cured product such as plasma treatment, UV treatment, or ozone treatment can be appropriately employed.

  The oxidizing agent may be an oxidizing agent available as a desmear liquid. Such an oxidizing agent can contain, for example, at least one permanganate selected from the group of sodium permanganate and potassium permanganate.

  When the hole plating 9 is provided, an initial wiring can be formed by subjecting a part of the roughened outer surface and the inner side surface of the hole 6 to electroless metal plating. Thereafter, the hole plating 9 can be formed by depositing a metal in the electrolyte plating solution on the initial wiring by electrolytic metal plating.

  An example of a method for producing a printed wiring board provided with a solder resist layer formed from the photosensitive resin composition according to the present embodiment will be described.

  First, a core material is prepared. The core material includes, for example, at least one insulating layer and at least one conductor wiring. A film is formed from the photosensitive resin composition on the surface of the core material where the conductor wiring is provided. Examples of the method for forming the film include a coating method and a dry film method. As the coating method and the dry film method, the same method as that for forming the interlayer insulating layer can be employed. The film is partially photocured by exposure. The exposure method can be the same as the method for forming the interlayer insulating layer. Subsequently, the film is subjected to a development process to remove the unexposed part of the film, whereby the exposed part of the film remains on the core material. Subsequently, the coating on the core material is heated and cured. The developing method and the heating method can be the same as the method for forming the interlayer insulating layer. If necessary, the film may be further irradiated with ultraviolet rays before or after heating. In this case, photocuring of the film can be further advanced.

  By the above, the solderless resist layer which consists of hardened | cured material of the photosensitive resin composition is provided on a core material. Thereby, a printed wiring board provided with the core material provided with an insulating layer and the conductor wiring on it, and the soldering resist layer which partially covers the surface in which the conductor wiring in a core material is provided is obtained. Note that the solder resist layer may be provided with a rough surface in the same manner as the interlayer insulating layer. Thereby, the adhesiveness of a soldering resist layer and the metal material which comprises conductor wiring, solder, etc. can be improved.

  In this embodiment, an electrically insulating layer such as a solder resist layer or an interlayer insulating layer can be formed particularly well from a dry film containing a dried product of the photosensitive resin composition. By providing a rough surface to this electrically insulating layer, the adhesion between the electrically insulating layer and the metal material can be improved.

  Hereinafter, the present invention will be specifically described by way of examples.

(1) Synthesis of carboxyl group-containing resin (1-1) Synthesis example A-1 to synthesis example A-4 and synthesis example B-1 to synthesis example B-3
The components shown in the “First Reaction” column of Table 1 are added to a four-necked flask equipped with a reflux condenser, thermometer, air blowing tube and stirrer, and the mixture is stirred by air bubbling. Was prepared. While stirring this mixture in the flask under air bubbling, the mixture was heated at the reaction temperature and reaction time shown in the “Reaction Conditions” column. This prepared an intermediate solution.

  Subsequently, the components shown in the “second reaction” column of Table 1 were added to the intermediate solution in the flask, and the reaction temperature and reaction time shown in the “reaction conditions (1)” column were stirred while air bubbling. Heated. Subsequently, with the exception of Synthesis Example B-1 to Synthesis Example B-3, the mixture was heated at the reaction temperature and reaction time shown in the “Reaction Conditions (2)” column with stirring under air bubbling. This obtained a 65 mass% solution of carboxyl group-containing resin. The polydispersity of the carboxyl group-containing resin (excluding the carboxyl group-containing resins in Synthesis Examples B-1 to B-3), the weight average molecular weight, and the acid value are as shown in Table 1. The molar ratio between the components is also shown in Table 1.

In addition, the detail of the component shown in the (a1) column of Table 1 is as follows.
Epoxy compound 1: A bisphenolfluorene type epoxy compound having an epoxy equivalent of 250 g / eq, represented by the formula (7), wherein R _{1 to} R ₈ in the formula (7) are all hydrogen.
Epoxy compound 2: epoxy equivalent 279 g represented by the formula (7), wherein R ₁ and R ₅ in the formula (7) are all methyl groups, and R _{2 to} R ₄ and R _{6 to} R ₈ are all hydrogen / Eq bisphenolfluorene type epoxy compound.

Moreover, the detail of the component shown in the (g1) column of Table 1 is as follows.
Epoxy compound 3: biphenyl novolac type epoxy resin (product name NC-3000-H manufactured by Nippon Kayaku Co., Ltd., epoxy equivalent 288 g / eq).
Epoxy compound 4: Cresol novolac type epoxy resin (manufactured by Nippon Steel & Sumikin Chemical Co., Ltd., product number YDC-700-5, epoxy equivalent 203 g / eq).
Epoxy compound 5: bisphenol A type epoxy resin (manufactured by Mitsubishi Chemical Corporation, product number jER1001, epoxy equivalent 472 g / eq).

Moreover, the detail of the component shown by the (a2) or (g2) column of Table 1 is as follows.
Ω-carboxy-polycaprolactone (n≈2) monoacrylate: manufactured by Toa Gosei Co., Ltd., trade name Aronix M-5300 (number average molecular weight 290).

[Examples 1 to 12, Comparative Examples 1 to 3]
A part of the components shown in the table below was kneaded with three rolls, and then all the components shown in the table below were stirred and mixed in the flask to obtain a photosensitive resin composition. When producing the photosensitive resin composition, the melamine compound (F) was uniformly dispersed in the photosensitive resin composition. In addition, the detail of the component shown by Table 2-Table 4 is as follows.
Unsaturated compound A: trimethylolpropane triacrylate.
Unsaturated compound B: ε-caprolactone-modified dipentaerystol hexaacrylate (manufactured by Nippon Kayaku Co., Ltd., product number KAYARAD DPCA-20).
Photopolymerization initiator A: 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide (product number Irgacure TPO, manufactured by BASF).
Photopolymerization initiator B: 1-hydroxy-cyclohexyl-phenyl-ketone (manufactured by BASF, product number Irgacure 184).
Photopolymerization initiator C: 4,4′-bis (diethylamino) benzophenone
Crystalline epoxy resin A: Biphenyl type crystalline epoxy resin (product name YX-4000 manufactured by Mitsubishi Chemical Corporation, melting point 105 ° C., epoxy equivalent 187 g / eq).
Crystalline epoxy resin B: Bisphenol type crystalline epoxy resin (product name YSLV-80XY manufactured by Nippon Steel & Sumikin Chemical Co., Ltd., melting point 75 to 85 ° C., 192 g / eq).
Amorphous epoxy resin C solution: long chain carbon chain-containing bisphenol A type epoxy resin (manufactured by DIC, part number EPICLON EXA-4816, liquid resin, epoxy equivalent 410 g / eq) at a solid content of 90% diethylene glycol monoethyl ether acetate (Epoxy equivalent in terms of solid content of 90% is 455.56 g / eq).
-Solution of amorphous epoxy resin D: Biphenyl novolac type epoxy resin (product name NC-3000, Nippon Kayaku Co., Ltd., softening point 53-63 ° C., epoxy equivalent 280 g / eq) at a solid content of 80% and diethylene glycol monoethyl A solution dissolved in ether acetate (epoxy equivalent in terms of solid content of 80% is 350 g / eq).
-Dispersion of organic filler A having carboxyl group: Dispersion (JSR) in which crosslinked rubber (NBR) having an average primary particle size of 0.07 μm is dispersed in methyl ethyl ketone at a content of 15% by weight with respect to the total amount of the dispersion. Product number XER-91-MEK; acid value 10.0 mgKOH / g).
-Dispersion of organic filler B having carboxyl group: Dispersion in which polymer (linear particles) of carboxyl group-modified hydrogenated nitrile rubber is dispersed in methyl ethyl ketone at a content of 17% by weight with respect to the total amount of the dispersion ( JSR Corporation, part number XER-32-MEK).
Dispersion of organic filler C having carboxyl group and hydroxyl group: Dispersion in which crosslinked rubber (SBR) having an average primary particle size of 0.07 μm is dispersed in methyl ethyl ketone at a content of 15% by weight with respect to the total amount of the dispersion. (JSR Co., Ltd., product number XSK-500).
Organic filler having an epoxy group: Glycidyl-modified acrylonitrile butadiene rubber in powder form and having an average primary particle size of 0.3 μm.
Melamine: manufactured by Nissan Chemical Industries, Ltd., fine melamine; dispersed in the photosensitive resin composition with an average particle size of 8 μm.
Melamine derivative: Melamine-tetrahydrophthalate which is a reaction product of melamine and 1,2,3,6-tetrahydrophthalic anhydride; dispersed in the photosensitive resin composition with an average particle size of 6 μm.
Antioxidant: A hindered phenol-based antioxidant (manufactured by BASF, product number IRGANOX 1010).
Silane coupling agent: 3-glycidoxypropyltrimethoxysilane.
Surfactant: manufactured by DIC, product number MegaFuck F-477.
-Rheology control agent: Product number BYK-430 manufactured by Big Chemie Japan Co., Ltd.
Solvent A: diethylene glycol monoethyl ether acetate.
Solvent B: methyl ethyl ketone.

[Production of test pieces]
Test pieces A and B were prepared using the photosensitive resin compositions of the examples and comparative examples as follows.

<Test piece A>
The photosensitive resin composition of each Example and Comparative Example was coated on a polyethylene terephthalate film with an applicator, and then dried by heating at 95 ° C. for 25 minutes, whereby a 25 μm thick dry film was formed on the film. A film was formed.

A glass epoxy copper clad laminate (FR-4 type) provided with a copper foil having a thickness of 17.5 μm was prepared. A comb-type electrode having a line width / space width of 50 μm / 50 μm was formed as a conductor wiring by this subtractive method on this glass epoxy copper clad laminate, thereby obtaining a printed wiring board (core material). The conductor wiring was roughened by dissolving and removing the surface portion of the printed wiring board having a thickness of about 1 μm with an etching agent (product number CZ-8100 manufactured by MEC Co., Ltd.). The dry film was heat laminated on the entire surface of the printed wiring board with a vacuum laminator. The heating lamination conditions were set to 0.5 MPa, 80 ° C., and 1 minute. Thereby, the membrane | film | coat consisting of the said dry film was formed on the printed wiring board. In a state where a negative mask having a non-exposed portion having a pattern including a circular shape with a diameter of 50 μm was directly applied to this film, the film was irradiated with ultraviolet rays through the negative mask under the condition of 250 mJ / cm ² . The exposed film was developed. In the development process, a 1% Na ₂ CO ₃ aqueous solution at 30 ° C. was sprayed onto the film for 90 seconds at a spray pressure of 0.2 MPa. Subsequently, pure water was sprayed onto the film at a spray pressure of 0.2 MPa for 90 seconds. Thereby, the part which was not exposed in a film | membrane was removed, and the hole was formed in the film | membrane. In addition, the film made from a polyethylene terephthalate was peeled from the said dry film after exposure. Subsequently, the film was irradiated with ultraviolet rays under the condition of 1000 mJ / cm ² . The film was then heated at 160 ° C. for 60 minutes. Thereby, the layer which consists of hardened | cured material (it can also be said to be hardened | cured material of a dry film) of the photosensitive resin composition was formed on the printed wiring board. Thereby, a test piece A was obtained.

<Test piece B>
Test piece B was obtained in the same procedure as test piece A, except that the thickness of the dry film formed from the photosensitive resin composition of each example and comparative example was 30 μm.

[Evaluation test]
(1) Developability About the test piece A of each Example and a comparative example, the non-exposed part of the printed wiring board after the said development process was observed, and the result was evaluated as follows.
Good: All the unexposed films are removed.
Inappropriate: A part of the unexposed film remained on the printed wiring board.

(2) Resolution About the test piece A of each Example and the comparative example, the hole formed in the layer which consists of hardened | cured material was observed, and the result was evaluated as follows.
A: The diameter of the bottom of the hole is 40 μm or more.
B: The diameter of the bottom of the hole is 25 μm or more and less than 40 μm.
C: The diameter of the bottom of the hole is less than 25 μm, or no clear hole is formed.

(3) Plating resistance A nickel plating layer is formed on a portion of the conductor wiring of the test piece A of each example and comparative example exposed to the outside using a commercially available electroless nickel plating bath. A gold plating layer was formed using an electroless gold plating bath. This formed the metal layer which consists of a nickel plating layer and a gold plating layer. The layer and metal layer which consisted of hardened | cured material were observed visually. Moreover, the cellophane adhesive tape peeling test was done with respect to the layer which consists of hardened | cured material. The results were evaluated as follows.
A: No abnormality was observed in the appearance of the layer made of the cured product and the metal layer, and peeling of the layer made of the cured product by the cellophane adhesive tape peeling test did not occur.
B: Although discoloration was recognized in the layer which consists of hardened | cured materials, peeling of the layer which consists of hardened | cured materials by the cellophane adhesive tape peeling test did not arise.
C: Lifting of the layer made of the cured product was observed, and peeling of the layer made of the cured product by the cellophane adhesive tape peeling test occurred.

(4) Insulation between lines While applying a bias voltage of DC 30 V to the conductor wiring (comb electrode) in the test piece A of each example and comparative example, the printed wiring board was placed at 121 ° C. and 97% R.D. H. The test environment was exposed for 100 hours. The electrical resistance value between the comb-shaped electrodes of the cured layer in this test environment was constantly measured, and the result was evaluated according to the following evaluation criteria.
A: The electric resistance value was constantly maintained at 10 ⁶ Ω or more until 100 hours passed from the start of the test.
B: The electric resistance value was always maintained at 10 ⁶ Ω or more until 80 hours passed from the start of the test, but the electric resistance value became less than 10 ⁶ Ω before 100 hours passed from the start of the test.
C: The electric resistance value was less than 10 ⁶ Ω before 80 hours passed from the start of the test.

(5) Interlayer insulation About the test piece A of each Example and the comparative example, the electrically conductive tape was affixed on the layer which consists of hardened | cured material. While applying a bias voltage of DC 100 V to this conductive tape, the test piece A was placed at 85 ° C. and 85% R.D. H. The test environment was exposed for 2000 hours. The electrical resistance value between the conductor wiring of the layer which consists of hardened | cured material in this test environment and a conductive tape was always measured, and the result was evaluated by the following evaluation criteria.
A: The electric resistance value was constantly maintained at 10 ⁸ Ω or more until 2000 hours passed from the start of the test.
B: The electric resistance value was always maintained at 10 ⁸ Ω or more until 1000 hours passed from the start of the test, but the electric resistance value became less than 10 ⁸ Ω before 2000 hours passed from the start of the test.
C: The electric resistance value was less than 10 ⁸ Ω before 1000 hours passed from the start of the test.

(6) PCT (pressure cooker test)
The test piece A of each Example and Comparative Example was left for 100 hours in an environment of 121 ° C. and 100% RH, and then the appearance of the cured layer was evaluated according to the following evaluation criteria.
A: No abnormality was found in the layer made of the cured product.
B: Discoloration was observed in the layer made of the cured product.
C: A large discoloration was observed in the layer made of the cured product, and partial swelling occurred.

(7) Roughening resistance About the test piece B of each Example and the comparative example, the outer surface of the layer which consists of hardened | cured material was roughened in the following procedure based on the general desmear process in the pre-process of plating process. Swelling treatment (Swelling Dip Securigans P manufactured by Atotech Japan Co., Ltd.) commercially available as a swelling liquid for desmear was performed at 60 ° C. for 5 minutes to swell the surface of the cured product. Then, the swollen surface was washed with hot water. Subsequently, using a oxidizer (concentrate compact CP manufactured by Atotech Japan Co., Ltd.) containing potassium permanganate and commercially available as a desmear liquid, roughening treatment is performed at 80 ° C. for 10 minutes, and after washing with hot water. The surface of the cured product was roughened. The surface of the cured product thus roughened is washed with hot water, and the residue of the desmear liquid on the surface of the cured product is further neutralized with a neutralizing solution (Reduction Solution Securigant P manufactured by Atotech Japan Co., Ltd.). And removed at 40 ° C. for 5 minutes. And the hardened | cured material surface after neutralization was washed with water. Thus, the film thickness of the film | membrane (layer which consists of hardened | cured material of the photosensitive resin composition) to which the rough surface was provided was measured, and the roughening tolerance of the hardened | cured material with respect to a desmear liquid was evaluated with the following evaluation criteria.
A: The decrease in film thickness due to roughening is less than 5 μm.
B: The reduction in film thickness due to roughening is 5 μm or more and less than 10 μm.
C: The reduction in film thickness due to roughening is 10 μm or more.

(8) Adhesiveness of copper plating layer About test piece B of each Example and a comparative example, after giving a rough surface to the layer which consists of hardened | cured material with the method of said (7), it is a test piece using a commercially available chemical | medical solution. Initial wiring was formed on the rough surface of B by electroless copper plating. Test piece B provided with the initial wiring was heated at 150 ° C. for 1 hour. Next, by electrolytic copper plating, copper having a thickness of 33 μm was directly deposited on the initial wiring from a commercially available chemical solution at a current density of ² A / dm ² , and then test piece B on which copper was deposited was deposited at 180 ° C. for 30 minutes. A copper plating layer was formed by heating for a minute. The adhesion between the copper plating layer thus formed and the cured product in the test piece B was evaluated according to the following evaluation criteria. Here, when a blister was not confirmed in the test piece B at the time of heating both after the electroless copper plating treatment and after the electrolytic copper plating treatment, the adhesion strength between the copper plating layer and the cured product was evaluated by the following procedure. This adhesion strength was measured according to JIS-C6481.
A: Blister was not confirmed at the time of heating after the electroless copper plating treatment, and no blister was confirmed at the time of heating after the electrolytic copper plating treatment. Moreover, the adhesive strength of copper was 0.4 kN / m or more.
B: Blister was not confirmed at the time of heating after electroless copper plating treatment, and blister was not confirmed at the time of heating after electrolytic copper plating treatment. Moreover, the adhesive strength of copper was less than 0.4 kN / m.
C: Blisters were confirmed during heating after the electroless copper plating treatment or during heating after the electrolytic copper plating treatment.

  The above results are shown in Tables 2 to 4.

Claims (8)

A carboxyl group-containing resin (A);
An unsaturated compound (B) having at least one ethylenically unsaturated bond in one molecule;
A photopolymerization initiator (C);
An epoxy compound (D);
An organic filler (E) containing an organic filler (E1) having a carboxyl group;
Containing at least one melamine compound (F) selected from the group of melamine and melamine derivatives,
Photosensitive resin composition.   The photosensitive resin composition of Claim 1 whose average primary particle diameter of the said organic filler (E1) is 1 micrometer or less.   The photosensitive resin composition of Claim 1 or 2 in which the said organic filler (E1) contains a rubber component.   The photosensitive resin composition according to claim 3, wherein the rubber component contains at least one polymer selected from the group of crosslinked acrylic rubber, crosslinked NBR, crosslinked MBS, and crosslinked SBR.   The photosensitive resin composition according to any one of claims 1 to 4, wherein the carboxyl group-containing resin (A) contains a carboxyl group-containing resin having a bisphenolfluorene skeleton.   The dry film containing the photosensitive resin composition as described in any one of Claims 1 thru | or 5.   A printed wiring board provided with the interlayer insulation layer containing the hardened | cured material of the photosensitive resin composition as described in any one of Claims 1 thru | or 5.   A printed wiring board provided with the soldering resist layer containing the hardened | cured material of the photosensitive resin composition as described in any one of Claims 1 thru | or 5.

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