JP5532307B2 - Method for producing phosphorus atom-containing polyfunctional phenol, phosphorus atom-containing polyfunctional phenol, curable resin composition, cured product thereof, printed wiring board resin composition, printed wiring board, flexible wiring board resin composition, semiconductor encapsulation A resin composition for a material and a resin composition for an interlayer insulating material for a build-up substrate. - Google Patents

Description

The present invention can easily introduce phosphorus atoms into the molecular structure of the polyfunctional phenol, and the obtained phosphorus atom-containing polyfunctional phenol has both excellent flame retardancy and heat resistance in the cured product. comprising a method for producing the phosphorus-containing polyfunctional phenols, phosphorus-containing polyfunctional phenols, and a curable resin composition using the same, the cured product, the printed wiring board resin composition for printed wiring board, flexible printed circuit board The present invention relates to a resin composition, a resin composition for a semiconductor sealing material, and a resin composition for an interlayer insulating material for a build-up substrate.

  An epoxy resin composition containing an epoxy resin and a curing agent as an essential component is excellent in various physical properties such as high heat resistance and moisture resistance, and is used for electronic components such as semiconductor encapsulants and printed circuit boards, electronic component fields, and conductive pastes. It is widely used in conductive adhesives such as, other adhesives, matrix for composite materials, paints, photoresist materials, developer materials, and the like.

  In recent years, in these various applications, especially in advanced materials, further improvements in performance typified by heat resistance, moisture resistance, and solder resistance have been demanded. In-vehicle electronic devices that require particularly high reliability, in addition to the shift from the cabin to the higher temperature engine room, the reflow processing temperature has increased due to the compatibility with lead-free solder. Therefore, there is a demand for a material that is more excellent in heat resistance than ever.

  On the other hand, when an epoxy resin composition is used as a printed wiring board material, a halogen-based flame retardant such as bromine is blended with an antimony compound in order to impart flame retardancy. However, in recent environmental and safety initiatives, environmentally and flame-resistant flame retardants that do not use halogen-based flame retardants that may cause dioxins and do not use antimony compounds that are suspected of carcinogenicity. There is a strong demand for the development of a conversion method. In the field of printed wiring board materials, the use of halogenated flame retardants is a factor that impairs reliability at high temperatures.

  In response to such required characteristics, as an epoxy resin composition having both flame retardancy and high heat resistance, for example, Patent Document 1 listed below discloses 9,10-dihydro-9- as a curing agent for epoxy resin. Phosphorus atoms obtained by reacting oxa-10-phosphaphenanthrene-10-oxide (hereinafter abbreviated as “HCA”) with formaldehyde or acetone to obtain a hydroxyl group-containing phosphorus compound, which is reacted with a phenol resin. A technique using a phenol resin containing a resin is disclosed. However, such a phosphorus atom-containing phenol resin has a low reactivity between polyfunctional phenol, HCA and aldehydes in the production process, and a reaction product of HCA and aldehydes is an unreacted component in the generated phenol resin. Although the cured product exhibits high flame retardancy, it is inferior in thermal decomposability and has recently been abbreviated as “T288 test”, which has been regarded as important for lead-free solder mounting in recent years. )). In addition, due to the low reactivity of the raw materials described above, the types of polyfunctional phenols that can be used are limited, and the design range of phosphorus atom-containing phenol resins is significantly limited.

  Patent Document 2 below discloses a compound obtained by reacting a reaction product of HCA and hydroxybenzaldehyde with phenol as an intermediate phenol compound of a phosphorus atom-containing epoxy resin.

  However, this phenolic compound also has a low degree of freedom in resin design due to insufficient reactivity between the reaction product of HCA and hydroxybenzaldehyde and phenol, and the final melting point of the phenolic compound is 200 ° C or higher. In addition to being difficult to manufacture industrially, the phenolic compound itself is a crystalline substance and is poor in solubility in an organic solvent, so that it is inferior in handling workability.

  In addition, in the following Patent Document 3, flame retardancy is obtained by using a phosphorus-modified epoxy resin obtained by reacting HCA with a phenol novolac type epoxy resin or a cresol novolak type epoxy resin as a main ingredient and blending with a curing agent for epoxy resin. An epoxy resin composition is disclosed. However, since the epoxy resin composition described in Patent Document 3 reacts with an epoxy group that originally becomes a crosslinking point as a means for introducing phosphorus atoms into the epoxy resin structure, a sufficient crosslinking density is obtained. In other words, the glass transition temperature of the cured product was lowered, so that it could not withstand lead-free solder mounting.

  As a means for imparting flame retardancy to the resin component itself as described above, although a technique using HCA as a modifier for a phenol resin or an epoxy resin is known, a reaction product of HCA and an aldehyde or a ketone has a phenol structure. When a phosphorus atom is to be introduced into the phenol structure by reacting with the aromatic nucleus therein, the heat resistance of the cured product of the phosphorus atom-containing phenol resin obtained due to the low reactivity of the reaction product is sufficient. In other words, the ability to withstand the heat-resistant peel test (hereinafter abbreviated as “T288 test”) was not exhibited. In addition, since the reactivity of the reaction product of HCA and aldehyde or ketone is low, phenols that can be used for the reaction with the reaction product are limited. On the other hand, when HCA is reacted with the epoxy group in the epoxy resin, the epoxy group concentration is lowered, so that sufficient heat resistance cannot be obtained.

Japanese Patent No. 3464783 Japanese Patent No. 3476780 Japanese Patent No. 3613724

Accordingly, an object of the present invention is to provide, as well as providing a significantly superior manufacturing method of the phosphorus atom-containing polyfunctional phenol reactivity when reacting the phosphorus-containing compound to the polyfunctional phenol aromatic nucleus, epoxy resin Phosphorus atom-containing polyfunctional phenol that gives excellent heat resistance to a cured product as a curing agent, a curable resin composition using the same, and a cured product thereof, and a printed wiring board resin using the phosphorus atom-containing polyfunctional phenol It is in providing the composition, the printed wiring board, the resin composition for flexible wiring boards, the resin composition for semiconductor sealing materials, and the resin composition for interlayer insulation materials for buildup boards.

As a result of intensive studies to solve the above-mentioned problems, the present inventors have reacted a phosphorus atom-containing compound typified by the HCA with an aromatic nucleus of a phenol resin having an alicyclic hydrocarbon group as a nodule group. First, the phosphorus atom-containing compound is reacted with an aromatic aldehyde having an alkoxy group as a substituent on the aromatic nucleus, and then the reaction product is converted into a plurality of phenolic compounds with an alicyclic hydrocarbon group as a linking group . When reacted with a polyfunctional phenol (a3) having a molecular structure to which a hydroxyl group-containing compound is bonded, the reactivity is drastically improved. However, a cured product of a phosphorus atom-containing polyfunctional phenol finally obtained As a result, the present invention was completed.

That is, the present invention reacts an aromatic aldehyde (a1) having an alkoxy group as a substituent on the aromatic nucleus and an organophosphorus compound (a2) having a P—H group or a P—OH group in the molecular structure. Then, the obtained reaction product is reacted with a polyfunctional phenol (a3) having a molecular structure in which a plurality of phenolic hydroxyl group-containing compounds are bonded with an alicyclic hydrocarbon group as a linking group. The present invention relates to a method for producing a phosphorus atom-containing polyfunctional phenol .

The present invention further relates to a phosphorus atom-containing polyfunctional phenol characterized by having a molecular structure obtained by the production method.

The present invention further includes the following structural formulas z1 to z4 as substituents on the aromatic nucleus of a polyfunctional phenol having a molecular structure in which a plurality of phenolic hydroxyl group-containing compounds are bonded with an alicyclic hydrocarbon group as a linking group.

（上記構造式ｚ１〜ｚ４中、Ｒ^１、Ｒ^２、Ｒ^３、Ｒ^４は、それぞれ独立的に、水素原子、炭素原子数１〜５のアルキル基、塩素原子、臭素原子、フェニル基、アラルキル基を表し、Ｒ５は水素原子又は炭素原子数１〜５のアルキル基を表し、Ｒは炭素原子１〜４のアルキル基を表し、ｎは芳香核上の置換基ＯＲの数であり１〜３である。）
で表される部分構造からなる群から選択される構造部位を有することを特徴とするリン原子含有多官能フェノールに関する。

(In the structural formulas z1 to z4, R ¹ , R ² , R ³ and R ⁴ are each independently a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a chlorine atom, a bromine atom, a phenyl group, or an aralkyl. R5 represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, R represents an alkyl group having 1 to 4 carbon atoms, n represents the number of substituents OR on the aromatic nucleus, and 1 to 3 .)
The present invention relates to a phosphorus atom-containing polyfunctional phenol characterized by having a structural moiety selected from the group consisting of the partial structures represented by the formula :

The present invention further relates to a curable resin composition which is polyfunctional phenol (A) and the epoxy resin (B) as essential components, wherein the polyfunctional phenol (A) is one obtained by the production method The present invention relates to a curable resin composition.

The present invention further relates to a curable resin composition which is polyfunctional phenol (A) and the epoxy resin (B) as essential components, wherein the polyfunctional phenol (A) is, in the phosphorus-containing polyfunctional phenols The present invention relates to a certain curable resin composition.

  The present invention further relates to a cured product obtained by curing the curable resin composition.

  The present invention further relates to a printed wiring board resin composition comprising the curable resin composition.

  The present invention further relates to a resin composition for a flexible wiring board comprising the curable resin composition.

  The present invention further relates to a printed wiring board obtained by impregnating a glass substrate with the curable resin composition and then curing the glass substrate.

  The present invention further relates to a resin composition for a semiconductor sealing material further containing an inorganic filler in addition to the curable resin composition.

  The present invention further relates to a resin composition for an interlayer insulating material for build-up substrates, comprising the curable resin composition.

ADVANTAGE OF THE INVENTION According to this invention, while providing the manufacturing method of the phosphorus atom containing polyfunctional phenol which is remarkably excellent in the reaction at the time of making a phosphorus atom containing compound react with the aromatic nucleus of polyfunctional phenol , it is hardened | cured material as a hardening | curing agent for epoxy resins. Phosphorus atom-containing polyfunctional phenol giving excellent heat resistance, curable resin composition using the same and cured product thereof, resin composition for printed wiring board using the phosphorus atom-containing polyfunctional phenol , and printed wiring board A resin composition for a flexible wiring board, a resin composition for a semiconductor sealing material, and a resin composition for an interlayer insulating material for a build-up board can be provided.

1 is a GPC chart of the polyfunctional phenol (A-1) obtained in Example 1. FIG. FIG. 2 is a GPC chart of the phenol resin (A-3) obtained in Comparative Example 1. FIG. 3 is a GPC chart of the phenol compound (A-4) obtained in Comparative Example 2. FIG. 4 is a GPC chart of the phenol resin (A-5) obtained in Comparative Example 3.

Hereinafter, the present invention will be described in detail.
In the production method of the present invention, as described above, an aromatic aldehyde (a1) having an alkoxy group as a substituent on the aromatic nucleus and an organophosphorus compound (a2) having a P—H group or a P—OH group are reacted. And then reacting the obtained reaction product with a polyfunctional phenol (a3) having a molecular structure in which a plurality of phenolic hydroxyl group-containing compounds are bonded with an alicyclic hydrocarbon group as a linking group. To do.

  The aromatic aldehyde (a1) having an alkoxy group as a substituent on the aromatic nucleus used here is, for example, benzaldehyde, o-tolualdehyde, p-tolualdehyde, o-ethylaldehyde, p-ethylaldehyde, p-isopropyl. Examples of aromatic aldehyde substituents such as benzaldehyde, naphthaldehyde, anthracene aldehyde, etc. include those having an alkoxy group. Specifically, the following structural formula (A1-a)

（式中、Ｒ^５は水素原子又は炭素原子１〜３のアルキル基であり、Ｒは炭素原子１〜４のアルキル基を表し、ｎは芳香核上の置換基ＯＲの数であり１〜３である。）
で表される化合物（ａ１−１）、或いは、下記構造式（Ａ１−ｂ）

Wherein R ⁵ is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, R represents an alkyl group having 1 to 4 carbon atoms, n is the number of substituents OR on the aromatic nucleus, and 1 to 3 .)
Or a compound represented by the following structural formula (A1-b)

（式中、Ｒ^５は水素原子又は炭素原子１〜３のアルキル基であり、Ｒは炭素原子１〜４のアルキル基を表し、ｎは芳香核上の置換基ＯＲの数であり１〜３である。）
で表される化合物（ａ１−２）が挙げられる。

Wherein R ⁵ is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, R represents an alkyl group having 1 to 4 carbon atoms, n is the number of substituents OR on the aromatic nucleus, and 1 to 3 .)
The compound (a1-2) represented by these is mentioned.

  In the present invention, among these, the compound (A1-a) is particularly preferable because the phosphorus content in one molecule is high, and particularly, n = 1 is preferable.

In the present invention, since the aromatic aldehyde (a1) has an alkoxy group as a nucleus substituent, the aromatic aldehyde (a1) and an organophosphorus compound (a2) having a P—H group or a P—OH group, The reactivity of the hydroxyl group produced in the reaction product is excellent, and the product reacts with the aromatic nucleus in the polyfunctional phenol (a3) even if almost no catalyst is used. The alkoxy group is preferably a methoxy group or an ethoxy group from the standpoint of such features, and the aromatic aldehyde is preferably benzaldehyde or naphthaldehyde.

  Specifically, the organophosphorus compound (a2) having an aromatic aldehyde (a1) and a reactive P—H group or P—OH group in the molecular structure is represented by the following structural formula (A2-a) or structural formula (A2- b)

（上記構造式（Ａ２−ａ）又は構造式（Ａ２−ｂ）中、Ｘａは水素原子又は水酸基であり、Ｒ^１、Ｒ^２、Ｒ^３、Ｒ^４はそれぞれ独立的に、水素原子、炭素原子数１〜５のアルキル基、塩素原子、臭素原子、フェニル基、アラルキル基を表す。）
で表される化合物が挙げられる。ここで、Ｒ^１、Ｒ^２、Ｒ３、Ｒ^４を構成する炭素原子数１〜５のアルキル基としては、メチル基、エチル基、ｎ−プロピル基、ｉ−プロピル基、ｔ−ブチル基、ｎ−ペンチル基が挙げられる。

(In the structural formula (A2-a) or the structural formula (A2-b), Xa is a hydrogen atom or a hydroxyl group, and R ¹ , R ² , R ³ , and R ⁴ are each independently a hydrogen atom or a carbon atom. Represents an alkyl group, a chlorine atom, a bromine atom, a phenyl group, or an aralkyl group of formulas 1 to 5.)
The compound represented by these is mentioned. ^Here, as R ^1, R 2, R3, an alkyl group having 1 to 5 carbon atoms constituting the ^{R 4,} a methyl group, an ethyl group, n- propyl group, i- propyl, t- butyl radical, n -A pentyl group is mentioned.

In the present invention, the structural formula (A2-a) or the structure is preferable in that the reactivity of the compound (X) produced by the reaction with the aromatic aldehyde (a1) with the polyfunctional phenol (a3) is extremely good. In the formula (A2-b), Xa is preferably a hydrogen atom, and the compound represented by the structural formula (A2-a) is particularly preferable from the viewpoint of excellent flame retardancy of a cured product of phosphorus atom-containing phenols. In particular, 9,10-dihydro-9-oxa-10 in which R ¹ , R ² , R ³ and R ⁴ are all hydrogen atoms and Xa is a hydrogen atom in the structural formula (A2-a). -It is phosphaphenanthrene-10-oxide, and the flame retardancy and heat resistance of the cured product of the phosphorus atom-containing polyfunctional phenol finally obtained are extremely good. It is preferable from the point.

  Here, the reaction conditions of the aromatic aldehyde (a1) having an alkoxy group as a substituent on the aromatic nucleus and the organophosphorus compound (a2) having a P—H group or a P—OH group are, for example, 80 to 180. It can be performed under the temperature condition of ° C. The reaction can be performed without a catalyst, or can be performed in the presence of a non-ketone organic solvent such as an alcohol organic solvent or a hydrocarbon organic solvent.

  The compound (X) produced by this reaction is, for example, a compound represented by the structural formula (a1-1) as the aromatic aldehyde (a1), a structural formula (a2-1) or the organic phosphorus compound (a2), or When the compound represented by the structural formula (a2-2) is used, the following structural formulas x1 to x4

（上記構造式ｘ１〜ｘ４中、Ｒ^１、Ｒ^２、Ｒ^３、Ｒ^４は、それぞれ独立的に、水素原子、炭素原子数１〜５のアルキル基、塩素原子、臭素原子、フェニル基、アラルキル基を表し、Ｒ５は水素原子又は炭素原子数１〜５のアルキル基を表し、Ｒは炭素原子１〜４のアルキル基を表し、ｎは芳香核上の置換基ＯＲの数であり１〜３である。）
が挙げられる。

(In the structural formulas x1 to x4, R ¹ , R ² , R ³ , and R ⁴ are each independently a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a chlorine atom, a bromine atom, a phenyl group, or an aralkyl. R5 represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, R represents an alkyl group having 1 to 4 carbon atoms, n represents the number of substituents OR on the aromatic nucleus, and 1 to 3 .)
Is mentioned.

Among these, the compounds represented by the structural formulas x1 and x2 are preferable from the viewpoint of excellent reactivity with the polyfunctional phenol (a3), and the flame retardant of a cured product of a phosphorus atom-containing polyfunctional phenol finally obtained is particularly preferable. The compound represented by the structural formula x1 is preferable from the viewpoint of excellent properties.

Next, the polyfunctional phenol (a3) used in the present invention has a molecular structure in which a plurality of phenolic hydroxyl group-containing compounds are bonded with an alicyclic hydrocarbon group as a linking group. Wherein the polyfunctional phenol (a3) a phenolic hydroxyl group-containing compound which is a raw material component constituting the, for example, phenol, cresol, xylenol, ethylphenol, isopropyl phenol, butylphenol, octylphenol, nonylphenol, vinylphenol, isopropenyl Examples include phenol, allylphenol, phenylphenol, benzylphenol, chlorophenol, bromophenol (each including o, m, and p-isomers), bisphenol A, naphthol, dihydroxynaphthalene, and the like. Among these, phenol and cresol are particularly preferable from the viewpoint of excellent fluidity and curability.

Further, the alicyclic hydrocarbon group constituting the polyfunctional phenol (a3) is preferable from the viewpoint of having a cyclohexane ring or cyclohexene ring is superior in water resistance improving effect of a cured product. Among these, since this effect is particularly remarkable, specifically, unsaturated groups such as dicyclopentadiene, tetrahydroindene, 4-vinylcyclohexene, 5-vinylnorborna-2-ene, α-pinene, β-pinene, and limonene. A divalent alicyclic hydrocarbon group derived from an unsaturated bond in the molecular skeleton of the alicyclic compound is preferable. These alicyclic hydrocarbon groups may be present alone or in combination of two or more. In addition, among these, a divalent complex alicyclic hydrocarbon group resulting from an unsaturated bond in the molecular skeleton of dicyclopentadiene from the viewpoint of excellent heat resistance and moisture resistance of the cured polyfunctional phenol finally obtained. It is preferable that

Here, when phenol or cresol is used as the phenolic hydroxyl group-containing compound and an alicyclic hydrocarbon group is used, the phenols (a3) are specifically represented by the following structural formula (a3-1) ).

ここで、式中、Ｒは水素原子又はメチル基であり、ｎは繰り返し単位の平均で０〜４である。

Here, in formula, R is a hydrogen atom or a methyl group, and n is 0-4 on the average of a repeating unit.

The polyfunctional phenol (a3) preferably has an ICI melt viscosity at 150 ° C. in the range of 0.1 to 40 dPa · s.

The reaction between the aromatic aldehyde (a1) and the compound (X), which is a reaction product of the organophosphorus compound (a2) having a P—H group or a P—OH group, with the polyfunctional phenol (a3), It can carry out under the temperature conditions of 140-200 degreeC. As described above, in the present invention, the reaction between the compound (X) and the polyfunctional phenol (a3) is extremely reactive and does not require a catalyst, but may be used as appropriate. Examples of catalysts that can be used here include inorganic acids such as hydrochloric acid, sulfuric acid, and phosphoric acid, organic acids such as methanesulfonic acid, p-toluenesulfonic acid, and oxalic acid, boron trifluoride, anhydrous aluminum chloride, and zinc chloride. Lewis acid etc. are mentioned. The amount used is preferably less than 5.0% by mass with respect to the total weight of the charged raw materials.

In the present invention, the reaction ratio between the compound (X) and the polyfunctional phenol (a3) is not particularly limited. Rather, because of its good reactivity, the desired flame retardancy and heat resistance are achieved. The modification amount of the compound (X) with respect to the polyfunctional phenol (a3) can be arbitrarily controlled according to the performance level or use. However, the reaction is such that the compound (X) does not remain in the reaction product, specifically, the reaction point on the aromatic nucleus of the polyfunctional phenol (a3) is equal to or less than the equivalent. Is preferred. Further, when the compound (X) is modified to a novolac type phenol resin or an aralkyl type phenol resin preferably used as the polyfunctional phenol (a3), the phosphorus atom content is 4.0 to 7.0 mass on a mass basis. % Is preferable because it is excellent in heat resistance and flame retardancy.

  After the reaction, the desired product can be obtained by dehydration and drying, if necessary. In the phosphorus atom-containing phenol resin thus obtained, the compound (X) that is an unreacted component hardly remains substantially. For example, when the compound (X) is modified into a novolac-type phenol resin or an aralkyl-type phenol resin and the phosphorus atom content is adjusted to a range of 4.0 to 7.0% by mass, the compound (X ) Is less than the detection limit of GPC in the phosphorus atom-containing phenol resin.

The phosphorus atom-containing polyfunctional phenol of the present invention has a molecular structure obtained by the production method described above. The specific molecular structure can be arbitrarily designed by selecting each of the raw material components described above, and has a molecular structure in which a plurality of phenolic hydroxyl group-containing compounds are bonded with an alicyclic hydrocarbon group as a linking group. As substituents on the aromatic nucleus of the functional phenol, the following structural formulas z1 to z4

（上記構造式ｚ１〜ｚ４中、Ｒ^１、Ｒ^２、Ｒ^３、Ｒ^４は、それぞれ独立的に、水素原子、炭素原子数１〜５のアルキル基、塩素原子、臭素原子、フェニル基、アラルキル基を表し、Ｒ^５は水素原子又は炭素原子数１〜５のアルキル基を表し、Ｒは炭素原子１〜４のアルキル基を表し、ｎは芳香核上の置換基ＯＲの数であり１〜３である。）
で表される部分構造からなる群から選択される構造部位を有する分子構造を有するものが挙げられる。

(In the structural formulas z1 to z4, R ¹ , R ² , R ³ and R ⁴ are each independently a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a chlorine atom, a bromine atom, a phenyl group, or an aralkyl. R ⁵ represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, R represents an alkyl group having 1 to 4 carbon atoms, n is the number of substituents OR on the aromatic nucleus, and 1 to 3)
Those having a molecular structure having a structural portion selected from the group consisting of the partial structures represented by the formula:

Furthermore, when phenol or cresol is used as the phenolic hydroxyl group-containing compound and an alicyclic hydrocarbon group is used, the phosphorus atom-containing polyfunctional phenol of the present invention is specifically represented by the following structural formula (PH -1).

ここで、式中、Ｒは水素原子又はメチル基であり、ｎは繰り返し単位の平均で０〜４であり、Ｚは、水素原子、又は、下記構造式ｚ１〜ｚ４

Here, in the formula, R is a hydrogen atom or a methyl group, n is an average of 0 to 4 repeating units, and Z is a hydrogen atom or the following structural formulas z1 to z4.

（上記構造式ｚ１〜ｚ４中、Ｒ^１、Ｒ^２、Ｒ^３、Ｒ^４は、それぞれ独立的に、水素原子、炭素原子数１〜５のアルキル基、塩素原子、臭素原子、フェニル基、アラルキル基を表し、Ｒ５は水素原子又は炭素原子数１〜５のアルキル基を表し、Ｒは炭素原子１〜４のアルキル基を表し、ｎは芳香核上の置換基ＯＲの数であり１〜３である。）
で表される部分構造からなる群から選択される構造部位であり、かつ、Ｚの少なくとも１つは前記構造式ｚ１〜ｚ４で表される部分構造からなる群から選択される構造部位である化学構造を有するものが挙げられる。

(In the structural formulas z1 to z4, R ¹ , R ² , R ³ and R ⁴ are each independently a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a chlorine atom, a bromine atom, a phenyl group, or an aralkyl. R5 represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, R represents an alkyl group having 1 to 4 carbon atoms, n represents the number of substituents OR on the aromatic nucleus, and 1 to 3 .)
A chemical moiety that is a structural moiety selected from the group consisting of the partial structures represented by the formula: and at least one of Z is a structural moiety selected from the group consisting of the partial structures represented by the structural formulas z1 to z4 those having a structure Ru mentioned.

  Further, among the partial structures represented by the structural formulas z1 to z4, the partial structure represented by the structural formula z1 or z2 is preferable from the viewpoint of excellent heat resistance of the cured product, and in particular, the structural formula z1. Those represented are preferred.

  Further, as described above, in the structural formula (PH-1), at least one of Z is a structural portion selected from the group consisting of partial structures represented by the structural formulas z1 to z4.

Moreover, in this invention, it is preferable from the point of a flame retardance that the phosphorus atom content rate in phosphorus atom containing polyfunctional phenol is a ratio used as 4.0-7.0 mass%, In said structural formula z1-z4, The represented partial structure is also preferably present in the phosphorus atom-containing polyfunctional phenol in such a ratio that satisfies the phosphorus content. The phosphorus atom content is a value calculated by the following formula based on the raw material charge and the raw material outflow during the reaction.

The curable resin composition of the present invention is a curable resin composition containing a polyfunctional phenol (A) and an epoxy resin (B) as essential components, and the phosphorus atom described above as the polyfunctional phenol (A). A polyfunctional phenol is used.

  Various epoxy resins can be used as the epoxy resin (B) used here, for example, bisphenol type epoxy resins such as bisphenol A type epoxy resin and bisphenol F type epoxy resin; biphenyl type epoxy resin, tetramethylbiphenyl type Biphenyl type epoxy resins such as epoxy resins; phenol novolak type epoxy resins, cresol novolak type epoxy resins, bisphenol A novolak type epoxy resins, epoxidized products of condensates of phenols and aromatic aldehydes having phenolic hydroxyl groups, biphenyl novolak type Novolak type epoxy resins such as epoxy resins; triphenylmethane type epoxy resins; tetraphenylethane type epoxy resins; dicyclopentadiene-phenol addition reaction type epoxy resins; Aralkyl epoxy resin; naphthol novolak epoxy resin, naphthol aralkyl epoxy resin, naphthol-phenol co-condensed novolac epoxy resin, naphthol-cresol co-condensed novolac epoxy resin, diglycidyloxynaphthalene, 1,1-bis (2, 7-diglycidyloxy-1-naphthyl) epoxy resins having a naphthalene skeleton in the molecular structure such as alkanes; phosphorus atom-containing epoxy resins. Moreover, these epoxy resins may be used independently and may mix 2 or more types.

Here, as the phosphorus atom-containing epoxy resin, epoxidized product of 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (hereinafter abbreviated as “HCA”), HCA and quinones Epoxy product of phenol resin obtained by reacting phenolic resin, epoxy resin obtained by modifying phenol novolac type epoxy resin with HCA, epoxy resin obtained by modifying cresol novolac type epoxy resin with HCA, and bisphenol A type epoxy resin using HCA and quinone An epoxy resin obtained by modifying a phenol resin obtained by reacting with a phenol, an epoxy resin obtained by modifying a bisphenol F type epoxy resin with a phenol resin obtained by reacting an HCA and a quinone, and the like Can be mentioned.
Among the above-mentioned epoxy resins (B), novolak type epoxy resins and epoxy resins having a naphthalene skeleton are preferable in the molecular structure particularly from the viewpoint of heat resistance, and bisphenol type epoxy resins and novolacs from the viewpoint of solvent solubility. Type epoxy resin is preferred.

  In the curable resin composition of this invention, you may use together the other hardening | curing agent (A ') of the said phenol resin (A) as a hardening | curing agent of an epoxy resin (B). Examples of such other curing agents (A ′) include amine compounds, amide compounds, acid anhydride compounds, phenol compounds, and the like. Specifically, examples of the amine compound include diaminodiphenylmethane, diethylenetriamine, triethylenetetramine, diaminodiphenylsulfone, isophoronediamine, imidazole, BF3-amine complex, and guanidine derivatives. Examples of the amide compound include dicyandiamide, Examples include polyamide resins synthesized from dimer of linolenic acid and ethylenediamine. Examples of acid anhydride compounds include phthalic anhydride, trimellitic anhydride, pyromellitic anhydride, maleic anhydride, and tetrahydrophthalic anhydride. , Methyltetrahydrophthalic anhydride, methyl nadic anhydride, hexahydrophthalic anhydride, methylhexahydrophthalic anhydride, etc., and phenolic compounds include phenol novolac resins, cresol novolac resins, Aromatic hydrocarbon formaldehyde resin modified phenolic resin, dicyclopentadiene phenol addition type resin, phenol aralkyl resin (Zyrock resin), naphthol aralkyl resin, trimethylol methane resin, tetraphenylol ethane resin, naphthol novolak resin, naphthol-phenol co-condensation Novolac resin, naphthol-cresol co-condensed novolak resin, biphenyl-modified phenol resin (polyhydric phenol compound with phenol nucleus linked by bismethylene group), biphenyl-modified naphthol resin (polyvalent naphthol compound with phenol nucleus linked by bismethylene group) , Aminotriazine-modified phenolic resin (compound having phenol skeleton, triazine ring and primary amino group in the molecular structure) and alkoxy group-containing aromatic ring-modified novolak Polyhydric phenol compounds such as fat (polyhydric phenol compound phenol nucleus and an alkoxy group-containing aromatic ring are connected by formaldehyde) and the like.

  Among these, those containing a large amount of an aromatic skeleton in the molecular structure are preferred from the viewpoint of low thermal expansion, and specifically, phenol novolac resins, cresol novolac resins, aromatic hydrocarbon formaldehyde resin-modified phenol resins, phenol aralkyls. Resin, naphthol aralkyl resin, naphthol novolak resin, naphthol-phenol co-condensed novolak resin, naphthol-cresol co-condensed novolak resin, biphenyl-modified phenol resin, biphenyl-modified naphthol resin, aminotriazine-modified phenol resin, alkoxy group-containing aromatic ring-modified novolak resin (Polyhydric phenol compound in which a phenol nucleus and an alkoxy group-containing aromatic ring are connected with formaldehyde) is preferable because of its low thermal expansion.

Here, the aforementioned aminotriazine-modified phenol resin, that is, a compound having a phenol skeleton, a triazine ring and a primary amino group in the molecular structure is a molecule obtained by condensation reaction of a triazine compound, a phenol and an aldehyde. What has a structure is preferable from the point which the flame retardance of hardened | cured material becomes favorable. Moreover, in this invention, the linear expansion coefficient in hardened | cured material is used by using what the nitrogen atom content rate in this compound (A'-b) becomes 10-25 mass%, Preferably it is 15-25 mass%. Is significantly reduced, and excellent dimensional stability can be exhibited.
Further, when the above-mentioned triazine compound, phenols and aldehydes are subjected to a condensation reaction, in practice, the compound (A′-b) is a mixture of various compounds. Hereinafter, it is preferably used as “mixture (A′-b)”. Furthermore, in this invention, it is preferable that it is the range from which the nitrogen atom content rate in the said mixture (A'-b) will be 10-25 mass%, especially 15-25 mass% from the point of a low point expansion coefficient.

  Here, the phenol skeleton represents a phenol structure site caused by phenols, and the triazine skeleton represents a triazine structure site caused by a triazine compound.

  The phenols used here are not particularly limited. For example, phenol, o-cresol, m-cresol, p-cresol, xylenol, ethylphenol, butylphenol, nonylphenol, octylphenol and other alkylphenols, bisphenol A Polyphenols such as bisphenol F, bisphenol S, bisphenol AD, tetramethylbisphenol A, resorcin, and catechol, naphthols such as monohydroxynaphthalene and dihydroxynaphthalene, and other phenylphenols and aminophenols. These phenols can be used alone or in combination of two or more. Phenols are preferred because the final cured product is excellent in flame retardancy and excellent in reactivity with amino group-containing triazine compounds.

  Next, the compound containing a triazine ring is not particularly limited, but the following structural formula

（式中、Ｒ’^１、Ｒ’^２、Ｒ’^３は、アミノ基、アルキル基、フェニル基、ヒドロキシル基、ヒドロキシルアルキル基、エーテル基、エステル基、酸基、不飽和基、シアノ基のいずれかを表わす。）
で表される化合物又はイソシアヌル酸が好ましい。

(In the formula, R ′ ¹ , R ′ ² and R ′ ³ are any of amino group, alkyl group, phenyl group, hydroxyl group, hydroxylalkyl group, ether group, ester group, acid group, unsaturated group, and cyano group. Represents.)
Or a compound represented by isocyanuric acid is preferred.

  Among the compounds represented by the structural formulas, melamine and acetoguanamine, in which any two or three of R′1, R′2, and R′3 are amino groups from the viewpoint of excellent reactivity. An amino group-containing triazine compound represented by a guanamine derivative such as benzoguanamine is preferable.

  These compounds are not limited to one kind in use, and two or more kinds may be used in combination.

  Next, aldehydes are not particularly limited, but formaldehyde is preferable from the viewpoint of easy handling. Although formaldehyde is not limited, Formalin, paraformaldehyde, etc. are mentioned as a typical supply source.

  Although it does not restrict | limit especially as a compounding quantity of the epoxy resin (B) and phenol resin (A) in the curable resin composition of this invention, From the point that the hardened | cured material characteristic obtained is favorable, an epoxy resin ( The amount by which the active hydrogen in the phenol resin (A) is 0.7 to 1.5 equivalents relative to a total of 1 equivalent of the epoxy groups of B) is preferred.

  Moreover, a hardening accelerator can also be suitably used together with the curable resin composition of this invention as needed. Various curing accelerators can be used, and examples thereof include phosphorus compounds, tertiary amines, imidazoles, organic acid metal salts, Lewis acids, and amine complex salts. In particular, when used as a semiconductor sealing material, it is excellent in curability, heat resistance, electrical characteristics, moisture resistance reliability, etc., so that triphenylphosphine is used for phosphorus compounds and 2-ethyl 4-methyl is used for amine compounds. Imidazole is preferred.

  As described above, the curable resin composition of the present invention described in detail above is characterized by exhibiting excellent solvent solubility. Therefore, the curable resin composition preferably contains an organic solvent (C) in addition to the above components. Examples of the organic solvent (C) that can be used here include methyl ethyl ketone, acetone, dimethylformamide, methyl isobutyl ketone, methoxypropanol, cyclohexanone, methyl cellosolve, ethyl diglycol acetate, propylene glycol monomethyl ether acetate, etc. The proper amount used can be appropriately selected depending on the application, but for example, in a printed wiring board application, it is preferable to use a polar solvent having a boiling point of 160 ° C. or lower, such as methyl ethyl ketone, acetone, 1-methoxy-2-propanol, etc. The non-volatile content is preferably 40 to 80% by mass. On the other hand, in the adhesive film use for build-up, as the organic solvent (C), for example, ketones such as acetone, methyl ethyl ketone, cyclohexanone, acetic acid such as ethyl acetate, butyl acetate, cellosolve acetate, propylene glycol monomethyl ether acetate, carbitol acetate, etc. Esters, carbitols such as cellosolve and butyl carbitol, aromatic hydrocarbons such as toluene and xylene, dimethylformamide, dimethylacetamide, N-methylpyrrolidone, etc. are preferably used, and non-volatile content is 30 to 60 mass. It is preferable to use it in the ratio which becomes%.

  The thermosetting resin composition is a non-halogen flame retardant that substantially does not contain a halogen atom in order to exert flame retardancy, for example, in the field of printed wiring boards, as long as the reliability is not lowered. May be blended.

  Examples of the non-halogen flame retardants include phosphorus flame retardants, nitrogen flame retardants, silicone flame retardants, inorganic flame retardants, and organic metal salt flame retardants. The flame retardants may be used alone or in combination, and a plurality of flame retardants of the same system may be used, or different types of flame retardants may be used in combination.

  As the phosphorus flame retardant, either inorganic or organic can be used. Examples of the inorganic compounds include red phosphorus, monoammonium phosphate, diammonium phosphate, triammonium phosphate, ammonium phosphates such as ammonium polyphosphate, and inorganic nitrogen-containing phosphorus compounds such as phosphate amide. .

  The red phosphorus is preferably subjected to a surface treatment for the purpose of preventing hydrolysis and the like. Examples of the surface treatment method include (i) magnesium hydroxide, aluminum hydroxide, zinc hydroxide, water A method of coating with an inorganic compound such as titanium oxide, bismuth oxide, bismuth hydroxide, bismuth nitrate or a mixture thereof; (ii) an inorganic compound such as magnesium hydroxide, aluminum hydroxide, zinc hydroxide, titanium hydroxide; and A method of coating with a mixture of a thermosetting resin such as a phenol resin, (iii) thermosetting of a phenol resin or the like on a coating of an inorganic compound such as magnesium hydroxide, aluminum hydroxide, zinc hydroxide, or titanium hydroxide For example, a method of double coating with a resin may be used.

Examples of the organic phosphorus compound include, for example, general-purpose organic phosphorus compounds such as phosphate ester compounds, phosphonic acid compounds, phosphinic acid compounds, phosphine oxide compounds, phosphorane compounds, organic nitrogen-containing phosphorus compounds, and 9,10- dihydro-9-oxa-10-phospha-phenanthrene-10-oxide, 10- (2,5-dihydroxy-phenyl) -10H-9-oxa-10-phospha-phenanthrene - 10-oxide, 10- (2,7 dihydroxy-naphthyl) -10H-9-oxa-10-phospha-phenanthrene - cyclic organic phosphorus compounds such as 10-oxide and derivatives in which it is reacted with a compound such as epoxy resin or phenol resin.

  The blending amount thereof is appropriately selected depending on the type of the phosphorus-based flame retardant, the other components of the curable resin composition, and the desired degree of flame retardancy. In 100 parts by mass of curable resin composition containing all of halogen-based flame retardant and other fillers and additives, 0.1 to 2.0 parts by mass of red phosphorus is used as a non-halogen flame retardant. It is preferable to mix in the range, and when using an organophosphorus compound, it is preferably mixed in the range of 0.1 to 10.0 parts by mass, particularly in the range of 0.5 to 6.0 parts by mass. It is preferable to do.

  In addition, when using the phosphorous flame retardant, the phosphorous flame retardant may be used in combination with hydrotalcite, magnesium hydroxide, boric compound, zirconium oxide, black dye, calcium carbonate, zeolite, zinc molybdate, activated carbon, etc. Good.

  Examples of the nitrogen-based flame retardant include triazine compounds, cyanuric acid compounds, isocyanuric acid compounds, phenothiazines, and the like, and triazine compounds, cyanuric acid compounds, and isocyanuric acid compounds are preferable.

  Examples of the triazine compound include melamine, acetoguanamine, benzoguanamine, melon, melam, succinoguanamine, ethylene dimelamine, melamine polyphosphate, triguanamine, and the like, for example, guanylmelamine sulfate, melem sulfate, melam sulfate, etc. Examples thereof include an aminotriazine sulfate compound, aminotriazine-modified phenol resin, and aminotriazine-modified phenol resin further modified with tung oil, isomerized linseed oil, and the like.

  Specific examples of the cyanuric acid compound include cyanuric acid and cyanuric acid melamine.

  The compounding amount of the nitrogen-based flame retardant is appropriately selected according to the type of the nitrogen-based flame retardant, the other components of the curable resin composition, and the desired degree of flame retardancy. For example, an epoxy resin, It is preferable to mix in the range of 0.05 to 10 parts by mass in 100 parts by mass of the curable resin composition containing all of the curing agent, non-halogen flame retardant and other fillers and additives. It is preferable to mix | blend in the range of 1-5 mass parts.

  Moreover, when using the said nitrogen-type flame retardant, you may use together a metal hydroxide, a molybdenum compound, etc.

  The silicone flame retardant is not particularly limited as long as it is an organic compound containing a silicon atom, and examples thereof include silicone oil, silicone rubber, and silicone resin.

  The amount of the silicone-based flame retardant is appropriately selected depending on the type of the silicone-based flame retardant, the other components of the curable resin composition, and the desired degree of flame retardancy. For example, an epoxy resin, It is preferable to mix in the range of 0.05 to 20 parts by mass in 100 parts by mass of the curable resin composition containing all of the curing agent, non-halogen flame retardant and other fillers and additives. Moreover, when using the said silicone type flame retardant, you may use a molybdenum compound, an alumina, etc. together.

  Examples of the inorganic flame retardant include metal hydroxide, metal oxide, metal carbonate compound, metal powder, boron compound, and low melting point glass.

  Specific examples of the metal hydroxide include aluminum hydroxide, magnesium hydroxide, dolomite, hydrotalcite, calcium hydroxide, barium hydroxide, zirconium hydroxide and the like.

  Specific examples of the metal oxide include, for example, zinc molybdate, molybdenum trioxide, zinc stannate, tin oxide, aluminum oxide, iron oxide, titanium oxide, manganese oxide, zirconium oxide, zinc oxide, molybdenum oxide, and cobalt oxide. Bismuth oxide, chromium oxide, nickel oxide, copper oxide, tungsten oxide and the like.

  Specific examples of the metal carbonate compound include zinc carbonate, magnesium carbonate, calcium carbonate, barium carbonate, basic magnesium carbonate, aluminum carbonate, iron carbonate, cobalt carbonate, and titanium carbonate.

  Specific examples of the metal powder include aluminum, iron, titanium, manganese, zinc, molybdenum, cobalt, bismuth, chromium, nickel, copper, tungsten, and tin.

  Specific examples of the boron compound include zinc borate, zinc metaborate, barium metaborate, boric acid, and borax.

  Specific examples of the low-melting-point glass include, for example, Shipley (Bokusui Brown), hydrated glass SiO2-MgO-H2O, PbO-B2O3-based, ZnO-P2O5-MgO-based, P2O5-B2O3-PbO-MgO-based, Examples thereof include glassy compounds such as P—Sn—O—F, PbO—V 2 O 5 —TeO 2, Al 2 O 3 —H 2 O, and lead borosilicate.

  The amount of the inorganic flame retardant is appropriately selected depending on the type of the inorganic flame retardant, the other components of the curable resin composition, and the desired degree of flame retardancy. For example, an epoxy resin, It is preferable to mix in the range of 0.05 to 20 parts by mass in 100 parts by mass of the curable resin composition containing all of the curing agent, non-halogen flame retardant and other fillers and additives. It is preferable to mix | blend in 5-15 mass parts.

  Examples of the organic metal salt flame retardant include ferrocene, acetylacetonate metal complex, organic metal carbonyl compound, organic cobalt salt compound, organic sulfonic acid metal salt, metal atom and aromatic compound or heterocyclic compound or an ionic bond or Examples thereof include a coordinated compound.

  The amount of the organic metal salt flame retardant is appropriately selected depending on the type of the organic metal salt flame retardant, the other components of the curable resin composition, and the desired degree of flame retardancy. In 100 parts by mass of the curable resin composition in which all of epoxy resin, curing agent, non-halogen flame retardant and other fillers and additives are blended, it is preferably blended in the range of 0.005 to 10 parts by mass. .

  An inorganic filler can be mix | blended with the curable resin composition of this invention as needed. Examples of the inorganic filler include fused silica, crystalline silica, alumina, silicon nitride, and aluminum hydroxide. When particularly increasing the blending amount of the inorganic filler, it is preferable to use fused silica. The fused silica can be used in either a crushed shape or a spherical shape. However, in order to increase the blending amount of the fused silica and suppress an increase in the melt viscosity of the molding material, it is preferable to mainly use a spherical shape. In order to further increase the blending amount of the spherical silica, it is preferable to appropriately adjust the particle size distribution of the spherical silica. The filling rate is preferably higher in consideration of flame retardancy, and particularly preferably 20% by mass or more with respect to the total amount of the curable resin composition. Moreover, when using for uses, such as an electrically conductive paste, electroconductive fillers, such as silver powder and copper powder, can be used.

  Various compounding agents, such as a silane coupling agent, a mold release agent, a pigment, an emulsifier, can be added to the curable resin composition of this invention as needed.

  The curable resin composition of the present invention can be obtained by uniformly mixing the above-described components. The curable resin composition of the present invention in which the epoxy resin of the present invention, a curing agent, and further, if necessary, a curing accelerator are blended can be easily made into a cured product by a method similar to a conventionally known method. Examples of the cured product include molded cured products such as laminates, cast products, adhesive layers, coating films, and films.

  Applications for use of the curable resin composition of the present invention include printed wiring board materials, resin compositions for flexible wiring boards, interlayer insulating materials for build-up boards, semiconductor sealing materials, conductive pastes, and adhesive films for build-ups Resin casting materials, adhesives, and the like. Among these various applications, in printed circuit boards, insulating materials for electronic circuit boards, and adhesive films for build-up, passive parts such as capacitors and active parts such as IC chips are embedded in so-called electronic parts. It can be used as an insulating material for a substrate. Among these, from the characteristics such as high flame retardancy, high heat resistance, low thermal expansibility, and solvent solubility, it is preferably used for a resin composition for a flexible wiring board, an interlayer insulating material for a build-up board, and a semiconductor sealing material. .

  Here, in order to produce a printed circuit board from the curable resin composition of the present invention, the varnish-like curable resin composition containing the organic solvent (D) is further blended with the organic solvent (D) to obtain a varnish. A method of impregnating a reinforced resin composition into a reinforcing base material and stacking a copper foil to heat-press is mentioned. Examples of the reinforcing substrate that can be used here include paper, glass cloth, glass nonwoven fabric, aramid paper, aramid cloth, glass mat, and glass roving cloth. If this method is described in further detail, first, the varnish-like curable resin composition is heated at a heating temperature corresponding to the solvent type used, preferably 50 to 170 ° C., thereby being a prepreg which is a cured product. Get. The mass ratio of the resin composition and the reinforcing substrate used at this time is not particularly limited, but it is usually preferable that the resin content in the prepreg is 20 to 60% by mass. Next, the prepreg obtained as described above is laminated by a conventional method, and a copper foil is appropriately stacked, and then subjected to thermocompression bonding at a pressure of 1 to 10 MPa at 170 to 250 ° C. for 10 minutes to 3 hours, A desired printed circuit board can be obtained.

In order to manufacture a flexible wiring board from the curable resin composition of the present invention, the polyfunctional phenol , the epoxy resin (B), the curing accelerator (C), and the organic solvent (D) are blended, and reverse. Using an applicator such as a roll coater or comma coater, it is applied to the electrically insulating film. Subsequently, it heats at 60-170 degreeC for 1 to 15 minutes using a heating machine, volatilizes a solvent, and B-stages an adhesive composition. Next, the metal foil is thermocompression bonded to the adhesive using a heating roll or the like. At that time, the pressure is preferably 2 to 200 N / cm and the pressure is preferably 40 to 200 ° C. If sufficient adhesive performance can be obtained, the process may be completed here. However, when complete curing is required, it is preferably post-cured at 100 to 200 ° C. for 1 to 24 hours. The thickness of the adhesive composition film after finally curing is preferably in the range of 5 to 100 μm.

In order to prepare a semiconductor sealing material from the curable resin composition of the present invention, in order to produce an epoxy resin composition prepared for a semiconductor sealing material, the polyfunctional phenol (A), the epoxy resin (B), a curing accelerator (C), and a compounding agent such as an inorganic filler are sufficiently melt-mixed until uniform using an extruder, kneader, roll, etc. as necessary. be able to. At that time, silica is usually used as the inorganic filler, and the filling rate is preferably in the range of 30 to 95% by mass of the filler per 100 parts by mass of the epoxy resin composition. 70 parts by mass or more is particularly preferable in order to improve the moisture resistance and solder crack resistance and decrease the linear expansion coefficient, and 80 parts by mass or more is more effective in order to significantly increase these effects. Can be increased. For semiconductor package molding, the composition is molded by casting, using a transfer molding machine, an injection molding machine or the like, and further heated at 50 to 200 ° C. for 2 to 10 hours to form a semiconductor device which is a molded product. There is a way to get

  As a method for obtaining an interlayer insulating material for a build-up substrate from the curable resin composition of the present invention, for example, the curable resin composition appropriately blended with rubber, filler, etc., spray coating method on a wiring board on which a circuit is formed, After applying using a curtain coating method or the like, it is cured. Then, after drilling a predetermined through-hole part etc. as needed, it treats with a roughening agent, forms the unevenness | corrugation by washing the surface with hot water, and metal-treats, such as copper. As the plating method, electroless plating or electrolytic plating treatment is preferable, and examples of the roughening agent include an oxidizing agent, an alkali, and an organic solvent. Such operations are sequentially repeated as desired, and a build-up base can be obtained by alternately building up and forming the resin insulating layer and the conductor layer having a predetermined circuit pattern. However, the through-hole portion is formed after the outermost resin insulating layer is formed. In addition, a resin-coated copper foil obtained by semi-curing the resin composition on the copper foil is thermocompression-bonded at 170 to 250 ° C. on a circuit board on which a circuit is formed, thereby forming a roughened surface and plating treatment. It is also possible to produce a build-up substrate by omitting the process.

  The method for producing an adhesive film for buildup from the curable resin composition of the present invention is, for example, a multilayer printed wiring board in which the curable resin composition of the present invention is applied on a support film to form a resin composition layer. And an adhesive film for use.

  When the curable resin composition of the present invention is used for a build-up adhesive film, the adhesive film is softened under the temperature condition of the laminate in the vacuum laminating method (usually 70 ° C. to 140 ° C.), and simultaneously with the lamination of the circuit board, It is important to show fluidity (resin flow) that allows resin filling in via holes or through holes present in a circuit board, and it is preferable to blend the above-described components so as to exhibit such characteristics.

  Here, the diameter of the through hole of the multilayer printed wiring board is usually 0.1 to 0.5 mm, and the depth is usually 0.1 to 1.2 mm. It is usually preferable to allow resin filling in this range. When laminating both surfaces of the circuit board, it is desirable to fill about 1/2 of the through hole.

  Specifically, the method for producing the adhesive film described above is, after preparing the varnish-like curable resin composition of the present invention, coating the varnish-like composition on the surface of the support film, further heating, Or it can manufacture by drying an organic solvent by hot air spraying etc. and forming the layer ((alpha)) of a curable resin composition.

  The thickness of the formed layer (α) is usually not less than the thickness of the conductor layer. Since the thickness of the conductor layer of the circuit board is usually in the range of 5 to 70 μm, the thickness of the resin composition layer is preferably 10 to 100 μm.

  In addition, the said layer ((alpha)) may be protected with the protective film mentioned later. By protecting with a protective film, it is possible to prevent dust and the like from being attached to the surface of the resin composition layer and scratches.

  The above-mentioned support film and protective film are made of polyolefin such as polyethylene, polypropylene and polyvinyl chloride, polyethylene terephthalate (hereinafter sometimes abbreviated as “PET”), polyester such as polyethylene naphthalate, polycarbonate, polyimide, and further. Examples thereof include metal foil such as pattern paper, copper foil, and aluminum foil. In addition, the support film and the protective film may be subjected to a release treatment in addition to the mud treatment and the corona treatment.

  Although the thickness of a support film is not specifically limited, Usually, it is 10-150 micrometers, Preferably it is used in 25-50 micrometers. Moreover, it is preferable that the thickness of a protective film shall be 1-40 micrometers.

  The above support film is peeled off after being laminated on a circuit board or after forming an insulating layer by heat curing. If the support film is peeled after the adhesive film is heat-cured, adhesion of dust and the like in the curing process can be prevented. In the case of peeling after curing, the support film is usually subjected to a release treatment in advance.

  Next, the method for producing a multilayer printed wiring board using the adhesive film obtained as described above is, for example, when the layer (α) is protected with a protective film, Lamination is performed on one or both sides of the circuit board by, for example, vacuum laminating so that α) is in direct contact with the circuit board. The laminating method may be a batch method or a continuous method using a roll. Further, the adhesive film and the circuit board may be heated (preheated) as necessary before lamination.

  The lamination conditions are such that the pressure bonding temperature (laminating temperature) is preferably 70 to 140 ° C., the pressure bonding pressure is preferably 1 to 11 kgf / cm 2 (9.8 × 10 4 to 107.9 × 104 N / m 2), and the air pressure is 20 mmHg (26 It is preferable to laminate under a reduced pressure of 0.7 hPa or less.

  When the curable resin composition of the present invention is used as a conductive paste, for example, a method of dispersing fine conductive particles in the curable resin composition to obtain a composition for anisotropic conductive film, liquid at room temperature And a paste resin composition for circuit connection and an anisotropic conductive adhesive.

  The method for obtaining the cured product of the present invention may be based on a general curing method for a curable resin composition, but for example, the heating temperature condition may be appropriately selected depending on the kind of curing agent to be combined and the use. However, what is necessary is just to heat the composition obtained by the said method in the temperature range of about room temperature-250 degreeC.

  Therefore, by using this phenol resin, the solvent solubility is dramatically improved compared to the conventional phenol resin modified with phosphorus, and when it is made into a cured product, flame retardancy, heat resistance and heat reliability can be expressed. Applicable to the most advanced printed wiring board materials. In addition, the phenol resin can be easily and efficiently produced by the production method of the present invention, and a molecular design corresponding to the target level of performance described above becomes possible.

Next, the present invention will be specifically described with reference to examples and comparative examples. The melt viscosity at 180 ° C., GPC measurement, NMR, and MS spectrum were measured under the following conditions.
1) Melt viscosity at 180 ° C .: in accordance with ASTM D4287 2) Softening point measurement method: JIS K7234
3) GPC: The measurement conditions are as follows.
Measuring device: “HLC-8220 GPC” manufactured by Tosoh Corporation
Column: Guard column “HXL-L” manufactured by Tosoh Corporation
+ "TSK-GEL G2000HXL" manufactured by Tosoh Corporation
+ "TSK-GEL G2000HXL" manufactured by Tosoh Corporation
+ Tosoh Corporation “TSK-GEL G3000HXL”
+ Tosoh Corporation “TSK-GEL G4000HXL”
Detector: RI (Differential refraction diameter)
Data processing: “GPC-8020 Model II version 4.10” manufactured by Tosoh Corporation
Measurement conditions: Column temperature 40 ° C
Developing solvent Tetrahydrofuran
Flow rate: 1.0 ml / min Standard: The following monodisperse polystyrene having a known molecular weight was used in accordance with the measurement manual of “GPC-8020 Model II version 4.10”.
(Polystyrene used)
“A-500” manufactured by Tosoh Corporation
"A-1000" manufactured by Tosoh Corporation
"A-2500" manufactured by Tosoh Corporation
"A-5000" manufactured by Tosoh Corporation
“F-1” manufactured by Tosoh Corporation
"F-2" manufactured by Tosoh Corporation
“F-4” manufactured by Tosoh Corporation
“F-10” manufactured by Tosoh Corporation
“F-20” manufactured by Tosoh Corporation
“F-40” manufactured by Tosoh Corporation
“F-80” manufactured by Tosoh Corporation
“F-128” manufactured by Tosoh Corporation
Sample: A 1.0 mass% tetrahydrofuran solution filtered in terms of resin solids and filtered through a microfilter (50 μl).

Example 1
In a flask equipped with a thermometer, a condenser tube, a fractionating tube, a nitrogen gas inlet tube and a stirrer, 222.2 g (1.35 mol) of dicyclopentadiene-type phenol resin and 54.5 g of p-anisaldehyde (0.33) Mol) and 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (hereinafter abbreviated as “HCA”) 72.0 g (0.33 mol) were charged, and the temperature was raised to 180 ° C. And reacted at 180 ° C. for 8 hours. Subsequently, water was removed under heating and reduced pressure to obtain a polyfunctional phenol (A-1) having the following structural units A and B as repeating units. The GPC chart of the obtained polyfunctional phenol (A-1) is shown in FIG. Moreover, the softening point of the obtained polyfunctional phenol (A-1) is 140 ° C. (B & R method), the melt viscosity (measurement method: ICI viscometer method, measurement temperature: 180 ° C.) is 80 dPa · s, and the hydroxyl group equivalent is 247 g. / Eq. The phosphorus content was 3.0% by mass.

Comparative Example 1 [Synthesis of Compound (Phenolic Resin (A-2)) described in Patent Document 1 (Patent No. 3464783)]
An eggplant flask was charged with 144 g (1.0 mol) of phenol novolac resin, and the temperature was raised to 100 ° C. with stirring in a nitrogen stream. After the temperature increase, 230 g (1.0 mol) of 2- (6-oxide-6H-dibenz <c, e><1,2> oxa-phosphorin-6-yl) methanol was added and heated to 140 ° C. And maintained for 12 hours. Subsequently, the mixture was cooled to room temperature, filtered and dried to obtain a phenol resin (A-2). The GPC chart of the obtained phenol resin (A-2) is shown in FIG.

Comparative Example 2 [Synthesis of Phenol Compound (Phenol Compound (A-3)) described in Patent Document 2 (Patent No. 3476780)]
A flask equipped with a thermometer, a condenser tube, a fractionating tube, a nitrogen gas inlet tube, and a stirrer is charged with 216 g (1.0 mol) of HCA and 216 g of toluene, heated to 110 ° C. and dissolved by heating. Next, 122 g (1.0 mol) of p-hydroxybenzaldehyde was charged, heated to 180 ° C. and reacted at 180 ° C. for 8 hours, followed by filtration and drying.

で表されるフェノール化合物（Ａ−３）を３３５ｇ得た。得られたフェノール化合物（Ａ−３）の融点は２８６℃であった。得られたフェノール化合物（Ａ−３）のＧＰＣチャートを図３に示す。

335 g of a phenol compound (A-3) represented by The melting point of the obtained phenol compound (A-3) was 286 ° C. The GPC chart of the obtained phenol compound (A-3) is shown in FIG.

Comparative Example 3 [Synthesis of phenol resin (A-4)]
In a flask equipped with a thermometer, a condenser tube, a fractionating tube, a nitrogen gas inlet tube, and a stirrer, 457.6 g (4.4 mol) of phenol novolac resin, 216 g (1.0 mol), and 122 g of p-hydroxybenzaldehyde ( 1.0 mol), the temperature was raised to 180 ° C., and the mixture was reacted at 180 ° C. for 8 hours. Next, water is removed under reduced pressure by heating, and the following structural units G and H

を繰り返し単位とするフェノール樹脂（Ａ−４）７５０ｇを得た。得られたフェノール樹脂の軟化点は１５０℃（Ｂ＆Ｒ法）、溶融粘度（測定法：ＩＣＩ粘度計法、測定温度：１５０℃）は１２０ｄＰａ・ｓ、水酸基当量は１６４ｇ／ｅｑ、リン含有量３．７質量％であった。得られたフェノール樹脂（Ａ−４）のＧＰＣチャートを図４に示す。

750 g of phenol resin (A-4) having a repeating unit was obtained. The softening point of the obtained phenol resin is 150 ° C. (B & R method), the melt viscosity (measurement method: ICI viscometer method, measurement temperature: 150 ° C.) is 120 dPa · s, the hydroxyl equivalent is 164 g / eq, and the phosphorus content is 3. It was 7 mass%. The GPC chart of the obtained phenol resin (A-4) is shown in FIG.

Example 2 and Comparative Examples 4-8
According to the formulation shown in Table 1, the epoxy resin composition was prepared by the following method, then cured under the following conditions, a laminate was produced as a prototype, and various evaluations were performed. The results are shown in Table 1.

[Adjustment of epoxy resin composition]
According to the composition shown in Table 1 below, an epoxy resin, a curing agent and other components were blended, and finally the nonvolatile content (NV) of the composition was adjusted to 58% by mass.

[Laminate production conditions]
Base material: 100 μm; glass cloth “# 2116” manufactured by Nitto Boseki Co., Ltd.
Number of plies: 6
Pre-pregation conditions: 160 ° C / 2 weight copper foil: 18µm; JTC foil curing condition manufactured by Nikko Metal Co., Ltd .: 200 ° C, 40kg / cm2 1.5 hours after molding Plate thickness: 0.8mm
[Physical property test conditions]
Glass transition temperature: measured by DMA method after etching and copper foil removal. Temperature rising speed 3 ° C / min.
Flame retardancy: Test method conforms to UL-94 vertical test.
Heat to peel test (Time to Delamination):
In accordance with IPC TM650, heat-resistant peelability evaluation (with copper foil) at 288 ° C. was performed.

Moisture absorption characteristics: Based on JIS-C-6481, the mass before and after storage for a predetermined time under the conditions of 121 ° C, 100% humidity and 2 atm using a pressure cooker tester “PC-304RIII” manufactured by Hirayama Seisakusho. The weight change was calculated as the moisture absorption rate.
Dielectric properties: 1 GHz of test piece after being stored in an indoor room at 23 ° C. and 50% humidity after being completely dried by impedance material analyzer “HP4291B” manufactured by Agilent Technologies, in accordance with JIS-C-6481 The dielectric constant and dielectric loss tangent at were measured.

Abbreviations in Table 1 are as follows.
“A-1”: polyfunctional phenol (A-1) obtained in Example 1
“A-2”: phenolic resin (A-2) obtained in Comparative Example 1
“A-3”: phenolic resin obtained in Comparative Example 2 (A-3)
“A-4”: phenolic resin obtained in Comparative Example 3 (A-4)
“J-DPP-85”: dicyclopentadiene type phenolic resin (“J-DPP-85” manufactured by Jinlong Chemical: 167 g / eq)
“TD-2090”: phenol novolac resin (“TD-2090” hydroxyl equivalent: 105 g / eq, manufactured by DIC),
“N-770”: phenol novolac type epoxy resin (“N-770” manufactured by DIC, epoxy equivalent of 185 g / eq),
“FX-289BER75”: Phosphorus-modified epoxy resin (“FX-289BER75” manufactured by Tohto Kasei: obtained by reacting cresol novolac type epoxy resin with 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide Epoxy resin, epoxy equivalent 330 g / eq., Phosphorus content 3.0 mass%)

Claims (16)

An aromatic aldehyde (a1) having an alkoxy group as a substituent on the aromatic nucleus and an organophosphorus compound (a2) having a P—H group or a P—OH group in the molecular structure were reacted, and then obtained. A phosphorus atom-containing polyfunctional phenol characterized by reacting a reaction product with a polyfunctional phenol (a3) having a molecular structure in which a plurality of phenolic hydroxyl group-containing compounds are bonded with an alicyclic hydrocarbon group as a linking group Manufacturing method. The process according to claim 1, wherein the aromatic aldehyde (a1) has a methoxy group or an ethoxy group as an alkoxy group in the aromatic aldehyde (a1). The organophosphorus compound (a2) having the P—H group or P—OH group in the molecular structure is represented by the following structural formula (A2-a) or structural formula (A2-b)

(In the structural formula (A2-a) or the structural formula (A2-b), R ¹ , R ² , R ³ , and R ⁴ are each independently a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, and chlorine. (Atom, bromine atom, phenyl group, aralkyl group, Xa represents a hydrogen atom or a hydroxyl group.)
The production method according to claim 1, wherein A novel phosphorus atom-containing polyfunctional phenol having a molecular structure obtained by the production method according to claim 1. As substituents on the aromatic nucleus of a polyfunctional phenol having a molecular structure in which a plurality of phenolic hydroxyl group-containing compounds are bonded using an alicyclic hydrocarbon group as a linking group, the following structural formulas z1 to z4 are used.

(In the structural formulas z1 to z4, R ¹ , R ² , R ³ and R ⁴ are each independently a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a chlorine atom, a bromine atom, a phenyl group, or an aralkyl. R5 represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, R represents an alkyl group having 1 to 4 carbon atoms, n represents the number of substituents OR on the aromatic nucleus, and 1 to 3 .)
A novel polyfunctional phenol having a structural moiety selected from the group consisting of partial structures represented by the formula: It is a curable resin composition which has a polyfunctional phenol (A) and an epoxy resin (B) as an essential component, Comprising: The said polyfunctional phenol (A) is a manufacture as described in any one of Claims 1-3. A curable resin composition obtained by the method. A curable resin composition comprising a polyfunctional phenol (A) and an epoxy resin (B) as essential components, wherein the polyfunctional phenol (A) is a novel phenol compound according to claim 5. object. The compounding ratio of the polyfunctional phenol (A) and the epoxy resin (B) is such that the active hydrogen in the polyfunctional phenol (A) is 0.1% with respect to a total of 1 equivalent of the epoxy groups of the epoxy resin (B). The curable resin composition according to claim 6 or 7, which has a ratio of 7 to 1.5 equivalents. The curable resin composition according to claim 6 or 7, further comprising a curing accelerator (C) in addition to the polyfunctional phenol (A) and the epoxy resin (B). The curable resin composition according to claim 9, further comprising an organic solvent (D) in addition to the components (A) to (C). A cured product obtained by curing the curable resin composition according to claim 6. The resin composition for printed wiring boards which consists of a composition of Claim 10. The resin composition for flexible wiring boards which consists of a composition of Claim 10. A printed wiring board obtained by impregnating a glass substrate with the composition according to claim 10 and then curing the glass substrate. The resin composition for semiconductor sealing materials which contains an inorganic filler in addition to the composition of Claim 9. The resin composition for interlayer insulation materials for buildup boards which consists of a composition of Claim 10.

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