JP2007246920A - Polyimide resin having phenolic hydroxyl group and polyimide resin composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a polyimide resin usable for varnish, adhesive and adhesive film, etc., to which adhesiveness and heat-resistance are required and provide a polyimide resin composition produced by using the resin. <P>SOLUTION: The invention provides a polyimide resin having repeating units expressed by structure formulas (1) and (2), produced by using a diamine having a phenolic hydroxyl group on an aromatic ring different from the aromatic ring bonded with amino group, and having a phenolic hydroxyl group in the skeleton. In the formulas, X is a tetravalent organic group; Y is a bivalent organic group composed of a diamine residue Y<SB>1</SB>having phenolic hydroxyl group and an aromatic diamine residue Y<SB>2</SB>; Z is a siloxanediamine residue; and m and n are each a natural number. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention relates to a polyimide resin suitable for various printed wiring boards, semiconductor package adhesives, sealing materials, and the like, which provides high adhesive strength, high reliability, and low elastic modulus, and a polyimide resin composition using the same. It is about.

  With recent downsizing and multi-functionalization of electronic devices, printed wiring boards and semiconductor package wirings are becoming more dense and finer. For this reason, there is a demand for adhesives with low-modulus materials that have high adhesion performance, reliability after moisture resistance, high-temperature processes during mounting, and that can relieve thermal stress when mounting electronic components. ing.

  Conventionally, low elastic modulus materials in which a siloxane structure is introduced into polyimide or polyamideimide, which are resins having excellent heat resistance, have been developed. JP-A-3-189127, JP-A-4-264003, and the like all propose siloxane-modified polyamideimides. However, these resins do not have sufficient adhesion to the copper foil and are not sufficiently heat resistant. Japanese Patent Application Laid-Open No. 10-60111 proposes that a compound having two or more maleimide groups is blended with a siloxane-modified polyamideimide to improve high-temperature characteristics. Inferior to sex. Japanese Patent No. 3221756 proposes a heat-resistant adhesive film of a polyimide silicone having a phenolic hydroxyl group and an epoxy resin. However, since the phenolic hydroxyl group exists in a three-dimensionally dense position, an epoxy resin is used. It is difficult to react with the hydroxyl group, and the bonding effect of the hydroxyl group produced by the reaction between the phenolic hydroxyl group and the epoxy resin cannot be expected.

Japanese Patent Laid-Open No. 3-189127 JP-A-4-264003 Japanese Patent Laid-Open No. 10-60111 Japanese Patent No. 3221756

  This invention is made | formed in view of the said situation, and it aims at providing the polyimide resin composition which provides the favorable performance of high adhesion | attachment, moisture-proof reliability, and a low elasticity modulus, and a polyimide resin composition containing this polyimide resin.

  As a result of intensive studies to eliminate the above-mentioned conventional drawbacks, the present inventor has used a diamine having a phenolic hydroxyl group in an aromatic ring different from the aromatic ring to which the amino group is bonded. A polyimide resin having a hydroxyl group has good reactivity with an epoxy resin, gives excellent performance to achieve the above-mentioned purpose, and this is used as an active ingredient, and preferably an epoxy resin having two or more glycidyl groups is blended therein. It has been found that the polyimide resin composition has high adhesion, moisture resistance reliability and low elastic modulus, and has led to the present invention.

［式中、Ｘは下記群［Ｉ］から選ばれる４価の有機基の１種又は２種以上、Ｙは、下記式［ＩＩ］で示されるフェノール性水酸基を有するジアミン残基Ｙ₁からなる２価の有機基、Ｚは下記式［ＩＶ］で示されるシロキサンジアミン残基であり、ｍ，ｎはそれぞれ自然数で、ｍ／（ｍ＋ｎ）は０．１〜０．９９であり、１０≦ｍ＋ｎ≦５００である。

（Ｒは、独立に水素原子、ハロゲン原子、又は置換もしくは非置換の炭素数１〜８の一価炭化水素基を示す。）

（Ａは下記群［ＩＩａ］から選ばれる基、Ｂは下記群［ＩＩｂ］から選ばれる基、

を示し、Ｒは上記と同様の意味を示し、ｋは１〜５の自然数である。）

（Ｒ¹は、独立に炭素数１〜８のアルキレン基又はアリーレン基、Ｒ²は、独立に炭素数１〜８のアルキル基、アルコキシ基又はアリール基を示し、ｊは４〜６０の整数を示す。）］
（ｉｉ）下記構造式（１）及び（２）で示される繰り返し単位を有し、ジアミンとしてアミノ基が結合した芳香族環とは異なる芳香族環にフェノール性水酸基を有するジアミンを用いて製造された、骨格中にフェノール性水酸基を有するポリイミド樹脂。

［式中、Ｘは下記群［Ｉ］から選ばれる４価の有機基の１種又は２種以上、Ｙは、下記式［ＩＩ］で示されるフェノール性水酸基を有するジアミン残基Ｙ₁と、下記群［ＩＩＩ］から選ばれる芳香族ジアミン残基Ｙ₂とからなる２価の有機基、Ｚは下記式［ＩＶ］で示されるシロキサンジアミン残基であり、Ｙ₁／（Ｙ₁＋Ｙ₂）はモル比で０．０１〜１であり、ｍ，ｎはそれぞれ自然数で、ｍ／（ｍ＋ｎ）は０．１〜０．９９であり、１０≦ｍ＋ｎ≦５００である。

（Ｒは、独立に水素原子、ハロゲン原子、又は置換もしくは非置換の炭素数１〜８の一価炭化水素基を示す。）

（Ａは下記群［ＩＩａ’］から選ばれる基、Ｂは下記群［ＩＩｂ］から選ばれる基、

を示し、Ｒは上記と同様の意味を示し、ｋは１〜５の自然数である。）

（Ｒは上記と同様の意味を示す。）

（Ｒ¹は、独立に炭素数１〜８のアルキレン基又はアリーレン基、Ｒ²は、独立に炭素数１〜８のアルキル基、アルコキシ基又はアリール基を示し、ｊは４〜６０の整数を示す。）］
（ｉｉｉ）下記構造式（１）及び（２）で示される繰り返し単位を有し、ジアミンとしてアミノ基が結合した芳香族環とは異なる芳香族環にフェノール性水酸基を有するジアミンを用いて製造された、骨格中にフェノール性水酸基を有するポリイミド樹脂。

［式中、Ｘは下記群［Ｉ］から選ばれる４価の有機基の１種又は２種以上、Ｙは、下記式［ＩＩ］で示されるフェノール性水酸基を有するジアミン残基Ｙ₁と、下記群［ＩＩＩ］から選ばれる芳香族ジアミン残基Ｙ₂とからなる２価の有機基、Ｚは下記式［ＩＶ］で示されるシロキサンジアミン残基であり、Ｙ₁／（Ｙ₁＋Ｙ₂）はモル比で０．０１〜１であり、ｍ，ｎはそれぞれ自然数で、ｍ／（ｍ＋ｎ）は０．１〜０．９９であり、１０≦ｍ＋ｎ≦５００である。

（Ｒは、独立に水素原子、ハロゲン原子、又は置換もしくは非置換の炭素数１〜８の一価炭化水素基を示す。）

（Ａは下記群［ＩＩａ］から選ばれる基、Ｂは下記群［ＩＩｂ’］から選ばれる基、

を示し、Ｒは上記と同様の意味を示し、ｋは１〜５の自然数である。）

（Ｒは上記と同様の意味を示す。）

（Ｒ¹は、独立に炭素数１〜８のアルキレン基又はアリーレン基、Ｒ²は、独立に炭素数１〜８のアルキル基、アルコキシ基又はアリール基を示し、ｊは４〜６０の整数を示す。）］ Accordingly, the present invention provides the following polyimide resins (i), (ii), and (iii).
(I) It is produced using a diamine having a repeating unit represented by the following structural formulas (1) and (2) and having a phenolic hydroxyl group on an aromatic ring different from the aromatic ring to which an amino group is bonded as a diamine. In addition, a polyimide resin having a phenolic hydroxyl group in the skeleton.

Wherein X is one or more tetravalent organic groups selected from the following group [I], and Y is a diamine residue Y ₁ having a phenolic hydroxyl group represented by the following formula [II]. A divalent organic group, Z is a siloxane diamine residue represented by the following formula [IV], m and n are natural numbers, m / (m + n) is 0.1 to 0.99, and 10 ≦ m + n ≦ 500.

(R independently represents a hydrogen atom, a halogen atom, or a substituted or unsubstituted monovalent hydrocarbon group having 1 to 8 carbon atoms.)

(A is a group selected from the following group [IIa], B is a group selected from the following group [IIb],

, R has the same meaning as described above, and k is a natural number of 1 to 5. )

(R ¹ independently represents an alkylene group or arylene group having 1 to 8 carbon atoms, R ² independently represents an alkyl group, alkoxy group or aryl group having 1 to 8 carbon atoms, and j represents an integer of 4 to 60. Shown]]]
(Ii) manufactured using a diamine having a repeating unit represented by the following structural formulas (1) and (2) and having a phenolic hydroxyl group on an aromatic ring different from the aromatic ring to which an amino group is bonded as a diamine. In addition, a polyimide resin having a phenolic hydroxyl group in the skeleton.

[Wherein X is one or more tetravalent organic groups selected from the following group [I], Y is a diamine residue Y ₁ having a phenolic hydroxyl group represented by the following formula [II], and A divalent organic group consisting of an aromatic diamine residue Y ₂ selected from the following group [III], Z is a siloxane diamine residue represented by the following formula [IV], and Y ₁ / (Y ₁ + Y ₂ ) Is a molar ratio of 0.01 to 1, m and n are natural numbers, m / (m + n) is 0.1 to 0.99, and 10 ≦ m + n ≦ 500.

(R independently represents a hydrogen atom, a halogen atom, or a substituted or unsubstituted monovalent hydrocarbon group having 1 to 8 carbon atoms.)

(A is a group selected from the following group [IIa ′], B is a group selected from the following group [IIb],

, R has the same meaning as described above, and k is a natural number of 1 to 5. )

(R has the same meaning as above.)

(R ¹ independently represents an alkylene group or arylene group having 1 to 8 carbon atoms, R ² independently represents an alkyl group, alkoxy group or aryl group having 1 to 8 carbon atoms, and j represents an integer of 4 to 60. Shown]]]
(Iii) It is produced using a diamine having a repeating unit represented by the following structural formulas (1) and (2) and having a phenolic hydroxyl group on an aromatic ring different from the aromatic ring to which an amino group is bonded as a diamine. In addition, a polyimide resin having a phenolic hydroxyl group in the skeleton.

[Wherein X is one or more tetravalent organic groups selected from the following group [I], Y is a diamine residue Y ₁ having a phenolic hydroxyl group represented by the following formula [II], and A divalent organic group consisting of an aromatic diamine residue Y ₂ selected from the following group [III], Z is a siloxane diamine residue represented by the following formula [IV], and Y ₁ / (Y ₁ + Y ₂ ) Is a molar ratio of 0.01 to 1, m and n are natural numbers, m / (m + n) is 0.1 to 0.99, and 10 ≦ m + n ≦ 500.

(R independently represents a hydrogen atom, a halogen atom, or a substituted or unsubstituted monovalent hydrocarbon group having 1 to 8 carbon atoms.)

(A is a group selected from the following group [IIa], B is a group selected from the following group [IIb ′],

, R has the same meaning as described above, and k is a natural number of 1 to 5. )

(R has the same meaning as above.)

(R ¹ independently represents an alkylene group or arylene group having 1 to 8 carbon atoms, R ² independently represents an alkyl group, alkoxy group or aryl group having 1 to 8 carbon atoms, and j represents an integer of 4 to 60. Shown]]]

  Furthermore, a polyimide resin composition containing a polyimide resin and preferably an epoxy resin having two or more glycidyl groups, more preferably an epoxy resin curing agent in addition to these is provided.

  The polyimide resin of the present invention and the polyimide resin composition using the same can be used for varnishes, adhesives, adhesive films and the like that require adhesiveness and heat resistance, and are used in the paint field, wiring board / electric field, automobile field, architecture field.・ Can be used widely in the building materials field. In addition, it exhibits not only excellent heat resistance, but also excellent properties such as drying properties, film moldability, and electrical properties as compared with conventional resins. Furthermore, when the resin composition is used as an interlayer insulating adhesive as an adhesive film, it prevents mechanical properties from being deteriorated by heating, improves interlayer insulation resistance and heat resistance reliability, and has not been able to cope with conventional resin systems. It can also be used in high temperature processes.

Hereinafter, the present invention will be described in more detail.
The polyimide resin of the present invention has a repeating unit represented by the following structural formulas (1) and (2), and a diamine having a phenolic hydroxyl group on an aromatic ring different from the aromatic ring to which an amino group is bonded as a diamine. It has a phenolic hydroxyl group in the skeleton produced by use.

Here, X is one or more tetravalent organic groups selected from the following group [I], Y is a diamine residue Y ₁ having a phenolic hydroxyl group represented by the following formula [II], and A divalent organic group consisting of an aromatic diamine residue Y ₂ selected from the group [III], Z is a siloxane diamine residue represented by the following formula [IV], and m and n are natural numbers, respectively, 10 ≦ It is m + n <= 500. In this case, m + n is preferably 20 to 400, m is 1 to 495, particularly 2 to 396, n is 5 to 499, particularly 4 to 398, and m / (m + n) is 0.1 to 0.3. 99, n / (m + n) is preferably from 0.01 to 0.9, and m / n is preferably from 0.02 to 50, particularly preferably from 0.1 to 40. On the other hand, the ratio of Y ₁ and Y ₂ are, Y ₁ / (Y ₁ + Y ₂₎ is 0.01 to 1 molar ratio, Y ₂ / (Y ₁ + Y ₂₎ is 0-0 molar ratio. 99, preferably Y ₁ / (Y ₁ + Y ₂ ) is 0.1 to 1 and Y ₂ / (Y ₁ + Y ₂ ) is 0 to 0.9.

（Ｒは、独立に水素原子、ハロゲン原子、又は置換もしくは非置換の炭素数１〜８の一価炭化水素基を示す。）

（Ａは下記群［ＩＩａ］から選ばれる基、Ｂは下記群［ＩＩｂ］から選ばれる基、

を示し、Ｒは上記と同様の意味を示し、ｋは１〜５の自然数である。）

（Ｒは上記と同様の意味を示す。）

（Ｒ¹は、独立に炭素数１〜８のアルキレン基又はアリーレン基、Ｒ²は、独立に炭素数１〜８のアルキル基、アルコキシ基又はアリール基を示し、ｊは４〜６０の整数を示す。）

(R independently represents a hydrogen atom, a halogen atom, or a substituted or unsubstituted monovalent hydrocarbon group having 1 to 8 carbon atoms.)

(A is a group selected from the following group [IIa], B is a group selected from the following group [IIb],

, R has the same meaning as described above, and k is a natural number of 1 to 5. )

(R has the same meaning as above.)

(R ¹ independently represents an alkylene group or arylene group having 1 to 8 carbon atoms, R ² independently represents an alkyl group, alkoxy group or aryl group having 1 to 8 carbon atoms, and j represents an integer of 4 to 60. Show.)

  Here, examples of the halogen atom for R include fluorine, bromine, iodine and the like, and examples of the monovalent hydrocarbon group include an alkyl group, an alkenyl group, an alkynyl group, an aryl group, and one of hydrogen atoms of these groups. Examples include groups in which part or all are substituted with halogen atoms such as fluorine atoms, methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, tert-butyl, hexyl, cyclohexyl, vinyl, allyl, propenyl, hexenyl, phenyl And trifluoromethyl.

Examples of the alkylene group for R ¹ include methylene, ethylene, trimethylene, tetramethylene, hexamethylene, and the arylene group includes phenylene. As R ² , in addition to the alkyl group exemplified for R above, an alkoxy group such as methoxy, ethoxy, propoxy, butoxy and the like, and an aryl group such as phenyl, tolyl, xylyl and the like can be mentioned. In addition, although j is an integer of 4-60, Preferably it is an integer of 5-40.

で示されるテトラカルボン酸二無水物あるいはこの前駆体であるテトラカルボン酸又はそのエステル誘導体と、下記一般式（４）、（５）及び（６）
Ｈ₂Ｎ−Ｙ₁−ＮＨ₂ （４）
Ｈ₂Ｎ−Ｙ₂−ＮＨ₂ （５）
Ｈ₂Ｎ−Ｚ−ＮＨ₂ （６）
で示されるジアミンとを反応させることにより得ることができる。但し、式（４）、（５）、（６）の各ジアミンの使用量をそれぞれｙ₁モル、ｙ₂モル、ｚモルとした場合、その比率は、ｙ₁／（ｙ₁＋ｙ₂）が０．０１〜１であり、（ｙ₁＋ｙ₂）／（ｙ₁＋ｙ₂＋ｚ）が０．１〜０．９９であり、またＸ，Ｙ₁（式［ＩＩ］），Ｙ₂（群［ＩＩＩ］），Ｚは上記した意味を示す。 The polyimide resin of the present invention has the following general formula (3)

A tetracarboxylic dianhydride or a precursor thereof, a tetracarboxylic acid or an ester derivative thereof, and the following general formulas (4), (5) and (6):
H ₂ N—Y ₁ —NH ₂ (4)
H ₂ N—Y ₂ —NH ₂ (5)
_{H 2 N-Z-NH 2} (6)
It can obtain by making it react with diamine shown by these. However, Equation (4), is (5), respectively y ₁ mole the amount of the diamine (6), y ₂ moles, when a z mol, the ratio, y ₁ / (y ₁ + y ₂₎ 0.01 to 1, (y ₁ + y ₂ ) / (y ₁ + y ₂ + z) is 0.1 to 0.99, and X, Y ₁ (formula [II]), Y ₂ (group [ III]) and Z have the meanings given above.

  Here, as tetracarboxylic dianhydride of the above formula (3) and its precursor tetracarboxylic acid and ester derivatives thereof, pyromellitic acid, 3,3 ′, 4,4′-benzophenonetetracarboxylic acid, 2,3,3 ′, 4′-biphenyltetracarboxylic acid, bis (3,4-carboxyphenyl) sulfone, 3,3 ′, 4,4′-biphenyltetracarboxylic acid, bis [4- (3,4- Dicarboxyphenoxy) phenyl] -methane, bis [4- (3,4-dicarboxyphenoxy) phenyl] -ethane, 2,2-bis [4- (3,4-dicarboxyphenoxy) phenyl] -propane, bis (3,4-dicarboxyphenyl) difluoromethane, 2,2-bis (3,4-dicarboxyphenyl) hexafluoropropane, 1,3-bis (3, -Dicarboxyphenyl) -1,1,3,3-tetratetramethylsiloxane, bis [4- (3,4-dicarboxyphenoxy) phenyl] methane, tetra such as bis (3,4-dicarboxyphenyl) ether It is 1 type, or 2 or more types chosen from reactive derivatives, such as carboxylic acid or these dianhydrides and ester.

で示されるもので（上記式中、Ｒ，ｋは上述した意味を表す）、これらを２種以上併用することもできる。 The diamine of formula (4) is as described above.

(In the above formula, R and k represent the above-mentioned meanings), and two or more of these may be used in combination.

  In this case, the amino group P of the diamine of formula (4) and the tetracarboxylic dianhydride of formula (3) or the acid anhydride residue (or 2 equivalents of carboxylic acid) of the precursor tetracarboxylic acid or ester derivative thereof. (Acid group or ester group) Q is required to react under the condition that the molar ratio of P / Q> 1 from the viewpoint of reducing esterification reaction by phenolic hydroxyl group and acid anhydride group, which is a side reaction. It is. More preferably, 2 ≦ P / Q ≦ 100, still more preferably 10 ≦ P / Q ≦ 100.

  The amount of the diamine having a phenolic hydroxyl group of the above formula (4) is preferably 1 mol% or more and 50 mol% or less with respect to all monomer components constituting the polyimide. Especially preferably, it is 5 mol% or more.

  Examples of the diamine of formula (5) include 4,4′-diaminodiphenylmethane, o-, m-, p-phenylenediamine, bis (4- (3-aminophenoxy) phenyl) sulfone, and 2,4-diaminotoluene. 2,5-diaminotoluene, 2,4-diaminoxylene, 2,4-diaminodurene, dimethyl-4,4′-diaminodiphenyl, dialkyl-4,4′-diaminodiphenyl, dimethoxy-4,4′- Diaminodiphenyl, diethoxy-4,4′-diaminodiphenyl, 4,4′-diaminodiphenyl ether, 3,4′-diaminodiphenyl ether, 4,4′-diaminodiphenyl sulfone, 3,3′-diaminodiphenyl sulfone, 4,4 '-Diaminobenzophenone, 3,3'-diaminobenzophenone, 1,3-bi (3-aminophenoxy) benzene, 1,3-bis (4-aminophenoxy) benzene, 1,4-bis (4-aminophenoxy) benzene, 4,4′-bis (4-aminophenoxy) biphenyl, bis ( 4- (4-aminophenoxy) phenyl) sulfone, 2,2′-bis (4- (4-aminophenoxy) phenyl) propane, 2,2-bis (4- (4-aminophenoxy) phenyl) hexafluoropropane 2,2-bis (4- (3-aminophenoxy) phenyl) propane, 2,2-bis (4- (3-aminophenoxy) phenyl) hexafluoropropane, 2,2-bis (4- (4- Amino-2-trifluoromethylphenoxy) phenyl) hexafluoropropane, 2,2-bis (4- (3-amino-5-trifluoromethyl) Enoxy) phenyl) hexafluoropropane, 2,2-bis (4-aminophenyl) hexafluoropropane, 2,2-bis (3-aminophenyl) hexafluoropropane, 2,2-bis (3-amino-4-) Hydroxyphenyl) hexafluoropropane, 2,2-bis (3-amino-4-methylphenyl) hexafluoropropane, 4,4′-bis (4-aminophenoxy) octafluorobiphenyl, 2,2′-bis (tri Fluoromethyl) diaminodiphenyl, 3,5-diaminobenzotrifluoride, 2,5-diaminobenzotrifluoride, 3,3′-bistrifluoromethyl-4,4′-diaminobiphenyl, 3,3′-bistrifluoromethyl- 5,5′-diaminobiphenyl, bis (trifluoromethyl) -4,4′- Diaminodiphenyl, bis (fluorinated alkyl) -4,4′-diaminodiphenyl, dichloro-4,4′-diaminodiphenyl, dibromo-4,4′-diaminodiphenyl, bis (fluorinated alkoxy) -4,4′- Diaminodiphenyl, diphenyl-4,4′-diaminodiphenyl, 4,4′-bis (4-aminotetrafluorophenoxy) tetrafluorobenzene, 4,4′-bis (4-aminotetrafluorophenoxy) octafluorobiphenyl, 4 , 4′-binaphthylamine, 4,4′-diaminobenzanilide, 4,4′-diamino (N-alkyl) benzanilide and the like, and two or more of these may be used in combination.

Incidentally, the formula proportion of a diamine and the diamine of formula (5) (4) (i.e., the ratio of the Y ₁ and Y ₂ in the structural formula) is, Y ₁ / (Y ₁ + Y ₂₎ is 1 to 100 mol% (i.e., 0.01 in molar ratio), a _{Y 2 / (Y 1 + Y} 2) is 0 to 99 mol% (i.e., 0 to 0.99 in molar ratio), preferably Y ₁ / (Y ₁ + Y ₂ ) is 10 to 100 mol%, and Y ₂ / (Y ₁ + Y ₂ ) is 0 to 90 mol%. When Y ₁ / (Y ₁ + Y ₂ ) is less than 1 mol%, good adhesion to the substrate cannot be expressed.

（Ｒ¹，Ｒ²，ｊは上述した意味を示す。）
で示されるもので、１，３−ビス（３−アミノプロピル）−１，１，２，２−テトラメチルジシロキサン、１，３−ビス（３−アミノブチル）−１，１，２，２−テトラメチルジシロキサン、ビス（４−アミノフェノキシ）ジメチルシラン、１，３−ビス（４−アミノフェノキシ）テトラメチルジシロキサン等が挙げられ、本発明のポリイミドに使用される式（６）のジアミノシロキサン成分は、ポリイミドを構成する全モノマー成分に対して１〜５０モル％が好ましく、より好ましくはポリイミドを構成する全モノマー成分の２〜４０モル％である。ジアミノシロキサン成分が１モル％未満では可撓性の付与効果に乏しく、５０モル％を超えると透湿性が上昇して、耐熱性の低下が認められるため好ましくない。 As described above, the diamine of formula (6) has the following formula:

(R ¹ , R ² , j have the above-mentioned meanings.)
1,3-bis (3-aminopropyl) -1,1,2,2-tetramethyldisiloxane, 1,3-bis (3-aminobutyl) -1,1,2,2 -Tetramethyldisiloxane, bis (4-aminophenoxy) dimethylsilane, 1,3-bis (4-aminophenoxy) tetramethyldisiloxane and the like, and the diamino of formula (6) used in the polyimide of the present invention The siloxane component is preferably 1 to 50 mol%, more preferably 2 to 40 mol% of the total monomer component constituting the polyimide, with respect to the total monomer component constituting the polyimide. If the diaminosiloxane component is less than 1 mol%, the effect of imparting flexibility is poor, and if it exceeds 50 mol%, moisture permeability increases and a decrease in heat resistance is observed.

  The production of a polyimide resin having a phenolic hydroxyl group in the skeleton of the present invention is a bifunctional amine component having a phenolic hydroxyl group in advance or a bifunctional amine component having a phenolic hydroxyl group and a bifunctional compound not containing a phenolic hydroxyl group. A mixture of the above amine components can be dispersed or dissolved in a reaction vessel, and a bifunctional or higher acid anhydride component can be dissolved or dispersed in a solvent and heated after dropwise stirring at a low temperature.

  As a solvent for polyimide, amide solvents such as N-methylpyrrolidone, N, N-dimethylformamide, N, N-dimethylacetamide and the like, which are usually employed, and oxygen-containing solvents include γ-butyrolactone, α Examples include lactones such as methyl-γ-butyrolactone, γ-valerolactone, δ-valerolactone, γ-caprolactone, and ε-caprolactone. In addition, carbonates such as ethylene carbonate and propylene carbonate, butyl acetate, and ethyl Esters such as cellosolve acetate and butylcellosolve acetate, ethers such as dibutyl ether, diethylene glycol dimethyl ether and triethylene glycol dimethyl ether, keto such as methyl isobutyl ketone, cyclohexanone and acetophenone In addition to alcohols such as butanol, octanol and ethyl cellosolve, chain or cyclic amides, ureas, sulfoxides, sulfones, hydrocarbons, and halogen solvents can affect polyimide stability. It is possible to add in the range which is not.

  Here, when the diamine and the tetracarboxylic dianhydride are reacted, the diamine having no phenolic hydroxyl group and the tetracarboxylic dianhydride are first reacted in the above-mentioned solvent to produce an amic acid oligomer. . Since this polyimide resin has a molar ratio of acid anhydride to amine of approximately 1: 1, an amic acid oligomer that does not contain a diamine having a phenolic hydroxyl group is rich in acid anhydride and has an acid anhydride group at the end. It is an oligomer. By dropping the acid anhydride-terminated amic acid oligomer solution into a diamine having a phenolic hydroxyl group, the diamine / acid anhydride ratio in the solution does not exceed 1, so that the polyimide resin having a phenolic hydroxyl group A polyamic acid having a phenolic hydroxyl group as a precursor is produced.

  Subsequently, by raising the temperature of the obtained polyamic acid solution in a temperature range of 80 to 250 ° C., preferably 120 to 200 ° C., a dehydration ring-closing reaction of the amide portion of the polyamic acid is advanced to obtain a polyimide resin solution. Moreover, an acetic anhydride / pyridine mixed solution can be added to a polyamic acid solution, and then the resulting solution can be heated to about 50 ° C. to perform imidization.

  The reason why the diamine / acid anhydride ratio in the solution does not exceed 1 is that when a diamine having a phenolic hydroxyl group is dropped under conditions where the acid anhydride is rich, an amide formation reaction is caused by the reaction between the carboxylic acid and the amine. In addition, esterification reaction by reaction of carboxylic acid and phenolic hydroxyl group also occurs at the same time, resulting in gelation by cross-linking in three dimensions. Since this gelled product has an ester bond structure, it undergoes a hydrolysis reaction under high-temperature and high-humidity conditions, lowers the molecular weight, and causes a decrease in moisture resistance reliability.

  In order to prevent the esterification reaction of the phenolic hydroxyl group and the acid anhydride-terminated amic acid oligomer solution, the amic acid oligomer is preferably dehydrated and cyclized to form an acid anhydride-terminated imide oligomer.

  In order to prevent the ester formation reaction due to the reaction between the phenolic hydroxyl group and the acid anhydride group, the phenolic hydroxyl group can be capped with a protecting group. However, the industrial cost is increased from the viewpoint of increasing the process cost and the material cost of the protecting group. It is not preferable for use.

  The weight average molecular weight of the polyimide resin of the present invention thus obtained is preferably 500 to 200,000, preferably 1,000 to 100,000, particularly 1,000 to 50,000.

  The polyimide resin of the present invention uses a diamine having a phenolic hydroxyl group in an aromatic ring such as a benzene ring or a naphthalene ring which is different from an aromatic ring such as a benzene ring to which an amino group is bonded. In particular, a polyimide resin composition in which an epoxy resin having two or more glycidyl groups and preferably a curing agent are blended with the polyimide resin has a low elastic modulus and is excellent in adhesiveness and reliability. Yes. If this resin composition is applied as a varnish on a support substrate, a film having excellent adhesion to a copper foil or the like can be obtained.

  There is no restriction | limiting in particular in the epoxy resin containing two or more glycidyl groups used by this invention. For example, glycidyl ethers of phenols such as bisphenol A, bisphenol F, resorcinol, phenol novolac, cresol novolac, glycidyl ethers of alcohols such as butanediol, polyethylene glycol, polypropylene glycol, phthalic acid, isophthalic acid, tetrahydrophthalic acid, etc. Glycidyl type (including methyl glycidyl type) epoxy resins such as those in which active hydrogen bonded to nitrogen atom such as glycidyl ester of carboxylic acid, aniline, isocyanuric acid or the like is substituted with glycidyl group, and olefin bond in molecule are epoxidized The resulting vinylcyclohexene diepoxide, 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate, 2- (3,4-epoxy) cyclohexane Of cycloaliphatic epoxy resin such as sil-5,5-spiro (3,4-epoxy) cyclohexane-m-dioxane, glycidyl ether of paraxylylene-modified phenol resin, glycidyl ether of metaxylylene-paraxylylene-modified phenol resin, terpene-modified phenol resin Examples include glycidyl ether, glycidyl ether of dicyclopentadiene modified phenolic resin, glycidyl ether of cyclopentadiene modified phenolic resin, glycidyl ether of polycyclic aromatic ring modified phenolic resin, glycidyl ether of naphthalene ring-containing phenolic resin, biphenyl type epoxy resin, etc. These can be used alone or in admixture of two or more.

  The epoxy resin curing agent of the present invention is not particularly limited as long as it works as a curing agent for epoxy resins, and examples thereof include phenolic compounds, acid anhydrides, amine compounds, etc. Among them, phenolic compounds are preferable. . Examples of the phenolic compound include phenols such as phenol, cresol, xylenol, hydroquinone, resorcin, catechol, bisphenol A, bisphenol F, or naphthols such as α-naphthol, β-naphthol, dihydroxynaphthalene, and formaldehyde, acetaldehyde, propionaldehyde. , A resin obtained by condensation or cocondensation with aldehydes such as benzaldehyde and salicylaldehyde under an acidic catalyst; a phenol resin having a xylylene skeleton synthesized from phenol and dimethoxyparaxylene; a phenol having a dicyclopentadiene skeleton Resin; Phenolic resin having cyclopentadiene skeleton; Melamine modified phenolic resin; Terpene modified phenolic resin; Polycyclic aromatic modified phenolic resin; Examples thereof include naphthol resins having a xylylene skeleton, and these can be used alone or in combination of two or more.

  The amount of the curing agent used is a curing effective amount, and a suitable blending amount varies depending on the specific type, but generally 1 to 100 parts by weight, preferably 5 to 50 parts by weight based on 100 parts by weight of the epoxy resin. The range is parts by weight. This is because when the amount of the curing agent used is less than 1 part by weight, it is difficult to cure the composition of the present invention satisfactorily, and conversely, when it exceeds 100 parts by weight, it is economically disadvantageous. This is because the resin is diluted to require a long time for curing, and further, the physical properties of the cured product are deteriorated.

  The epoxy resin curing catalyst used in the present invention is not particularly limited, and examples of the phosphorus catalyst include triphenylphosphine, triphenylphosphonium triphenylborate, tetraphenylphosphonium tetraphenylborate, and compounds as shown below.

（式中、Ｒ³〜Ｒ¹⁰は、水素原子、フッ素、臭素、ヨウ素などのハロゲン原子、炭素数が１〜８のアルキル基、アルケニル基、アルキニル基、炭素数が１〜８のアルコキシ基、トリフルオロメチル基、フェニル基などが挙げられ、総ての置換基が同一でも異なっていてもよい。）

(Wherein R ^{3 to} R ¹⁰ are a hydrogen atom, a halogen atom such as fluorine, bromine or iodine, an alkyl group having 1 to 8 carbon atoms, an alkenyl group, an alkynyl group, an alkoxy group having 1 to 8 carbon atoms, (A trifluoromethyl group, a phenyl group, etc. are mentioned, and all the substituents may be the same or different.)

  Further, as the amine catalyst, imidazole derivatives such as 2-methylimidazole, 2-ethyl-4-methylimidazole, 1-cyanoethyl-2-methylimidazole, 2-phenyl-4,5-dihydroxymethylimidazole, and the like are blended. Of these, one or more of them can be used.

  Although the chemical equivalent ratio of the sum total of the epoxy resin hardening | curing agent with respect to an epoxy resin and the polyimide resin which has a phenolic hydroxyl group in frame | skeleton is not restrict | limited, It is preferable to set to the range of 0.7-1.3. More preferably, it is 0.8-1.2. This is effective in suppressing the respective unreacted components to a small extent and reducing the deterioration over time such as the adhesive strength, the water absorption amount, and the electrical characteristics.

  The blending ratio of the polyimide resin having a phenolic hydroxyl group in the skeleton of the present invention, the epoxy resin, and the epoxy resin curing agent is important. In the present invention, the curing reaction is carried out by utilizing the reaction between a phenolic hydroxyl group and an epoxy group. If there are too few epoxy groups, the adhesive force with the adherend is not sufficient, and if there are too many, the excess epoxy resin This increases the elastic modulus, which is unsuitable for producing a flexible polyimide resin composition. Therefore, the mixture of the epoxy resin and the epoxy resin curing agent is 1 to 900 parts by weight, preferably 5 to 400 parts by weight with respect to 100 parts by weight of the polyimide resin.

  Moreover, the compounding quantity of the said epoxy resin curing catalyst is 40 weight part or less (0-40 weight part) normally with respect to a total of 100 weight part of an epoxy resin and an epoxy resin hardening | curing agent, Preferably it is 0.01-40 weight. Part, more preferably about 0.1 to 20 parts by weight. If the amount of the epoxy resin curing catalyst is too small, it may take a long time for curing, or sufficient curability may not be obtained, and if it is too large, the storage stability of the composition may be poor.

  The polyimide resin composition of the present invention is desirably well stirred for 5 minutes or more in order not to separate the components after blending the above components. The polyimide resin composition thus obtained is soluble in aprotic polar solvents such as cyclohexanone and NMP and can be used as it is as a varnish.

  If the polyimide resin composition of this invention is apply | coated on a support base material, the film | membrane excellent in adhesiveness with copper foil etc. can be obtained. This film can be cured by heating usually at 160 ° C. or higher, preferably 200 ° C. or higher.

  EXAMPLES Hereinafter, although an Example and a comparative example are shown and this invention is demonstrated concretely, this invention is not restrict | limited to the following Example. In addition, in the following example, a part shows a weight part.

[Synthesis Example 1]
Linear dimethyl having both ends of the molecular chain blocked with γ-aminopropyldimethylsiloxy group in a 25 ml moisture meter with a cock connected to a reflux condenser, a thermometer and a 1 L separable flask equipped with a stirrer Polysiloxane: 44.03 parts of KF-8010 (manufactured by Shin-Etsu Chemical Co., Ltd.) and 100 parts of cyclohexanone as a reaction solvent were added and stirred at 80 ° C. to disperse the diamine. By adding dropwise a solution of 38.72 parts of 6FDA (2,2-bis (3,4-dicarboxyphenyl) hexafluoropropane) and 100 parts of cyclohexanone as an acid anhydride and performing a stirring reaction at 80 ° C. for 8 hours, An acid anhydride-rich amic acid oligomer was synthesized.

  Next, a 25 ml water quantitative receiver, thermometer and stirrer with a cock in which 17.25 parts of aromatic diamine (diamine-1) having a phenolic hydroxyl group shown below and 100 parts of cyclohexanone are connected to a reflux condenser are connected. Were placed in a 1 L separable flask and dispersed, and the acid anhydride-rich polyamic acid solution was added dropwise. Thereafter, 25 ml of toluene was added, the temperature was raised, and the mixture was refluxed at about 160 ° C. for 2 hours. Make sure that a predetermined amount of water has accumulated in the moisture meter and that no water has flowed out. Remove the effluent that has accumulated in the moisture meter and completely remove toluene at 160 ° C. Removed. After completion of the reaction, 400 parts of a cyclohexanone solution of a polyimide resin having a phenolic hydroxyl group in the skeleton was obtained. The solvent of the obtained solution was distilled off and then dried under reduced pressure to obtain a polyimide resin.

When the infrared absorption spectrum of the obtained resin was measured, absorption based on polyamic acid indicating that there was an unreacted functional group did not appear, and absorption based on an imide group was confirmed at 1780 cm ⁻¹ and 1720 cm ⁻¹ . Absorption based on a phenolic hydroxyl group was confirmed at 3500 cm ⁻¹ . It was 30000 when the weight average molecular weight (polystyrene conversion) of this resin was measured by the gel permeation chromatography (GPC) which uses tetrahydrofuran as a solvent. The glass transition point determined by thermomechanical measurement was 115 ° C.

[Synthesis Example 2]
Linear dimethyl having both ends of the molecular chain blocked with γ-aminopropyldimethylsiloxy group in a 25 ml moisture meter with a cock connected to a reflux condenser, a thermometer and a 1 L separable flask equipped with a stirrer Polysiloxane: 44.03 parts of KF-8010 (manufactured by Shin-Etsu Chemical Co., Ltd.) and 100 parts of cyclohexanone as a reaction solvent were added and stirred at 80 ° C. to disperse the diamine. By adding dropwise a solution of 38.72 parts of 6FDA (2,2-bis (3,4-dicarboxyphenyl) hexafluoropropane) and 100 parts of cyclohexanone as an acid anhydride and performing a stirring reaction at 80 ° C. for 8 hours, An acid anhydride-rich amic acid oligomer was synthesized.

  Thereafter, 25 ml of toluene was added, the temperature was raised, and the mixture was refluxed at about 160 ° C. for 2 hours. Make sure that a predetermined amount of water has accumulated in the moisture meter and that no water has flowed out. Remove the effluent that has accumulated in the moisture meter and completely remove toluene at 160 ° C. To obtain an acid anhydride-rich imide solution.

  Next, 17.25 parts of the aromatic diamine (diamine-1) having a phenolic hydroxyl group shown above and 100 parts of cyclohexanone with a 25 ml water quantitative receiver, thermometer, and stirrer connected with a reflux condenser Was added to a 1 L separable flask and dispersed, and the imide solution rich in acid anhydride was added dropwise. Thereafter, 25 ml of toluene was added, the temperature was raised, and the mixture was refluxed at about 160 ° C. for 2 hours. Make sure that a predetermined amount of water has accumulated in the moisture meter and that no water has flowed out. Remove the effluent that has accumulated in the moisture meter and completely remove toluene at 160 ° C. Removed. After completion of the reaction, 400 parts of a cyclohexanone solution of a polyimide resin having a phenolic hydroxyl group in the skeleton was obtained. The solvent of the obtained solution was distilled off and then dried under reduced pressure to obtain a polyimide resin.

When the infrared absorption spectrum of the obtained resin was measured, absorption based on polyamic acid indicating that there was an unreacted functional group did not appear, and absorption based on an imide group was confirmed at 1780 cm ⁻¹ and 1720 cm ⁻¹ . Absorption based on a phenolic hydroxyl group was confirmed at 3500 cm ⁻¹ . It was 32000 when the weight average molecular weight (polystyrene conversion) of this resin was measured by the gel permeation chromatography (GPC) which uses tetrahydrofuran as a solvent. The glass transition point by thermomechanical measurement was 120 ° C.

[Synthesis Example 3]
17.25 parts of aromatic diamine (diamine-1) having a phenolic hydroxyl group as shown above in a 1 L separable flask equipped with a 25 ml moisture meter with a cock connected to a reflux condenser, a thermometer, and a stirrer , 44.03 parts linear dimethylpolysiloxane blocked at both ends of the molecular chain with γ-aminopropyldimethylsiloxy groups: KF-8010 (manufactured by Shin-Etsu Chemical Co., Ltd.), 200 parts of cyclohexanone as a reaction solvent, The mixture was stirred at 80 ° C to disperse the diamine. Then, a solution of 38.72 parts of 6FDA (2,2-bis (3,4-dicarboxyphenyl) hexafluoropropane) and 100 parts of cyclohexanone was added dropwise as an acid anhydride and stirred at 80 ° C. for 8 hours. However, a gelled product was formed. Thereafter, 25 ml of toluene was added, the temperature was raised, and the mixture was refluxed at about 160 ° C. for 2 hours. After confirming that water had accumulated in the moisture determination receiver and that no water was flowing out, toluene was completely removed at 160 ° C. while removing the effluent accumulated in the moisture determination receiver. . After completion of the reaction, 400 parts of a cyclohexanone solution of a polyimide resin having a phenolic hydroxyl group in the skeleton was obtained. The solvent of the obtained solution was distilled off and then dried under reduced pressure to obtain a polyimide resin.

The infrared absorption spectrum of the obtained resin was measured, appear absorption based on amic acid 3200 cm ^-1 and 3300 cm ^-1 indicating the presence of unreacted functional groups, imido groups in 1780 cm ^-1 and 1720 cm ^-1 The absorption based on phenolic hydroxyl group was confirmed, and the absorption based on phenolic hydroxyl group was confirmed at 3500 cm ⁻¹ . It was 25000 when the weight average molecular weight (polystyrene conversion) of this resin was measured by the gel permeation chromatography (GPC) which uses tetrahydrofuran as a solvent. The glass transition point measured by thermomechanical measurement was 100 ° C.

[Synthesis Examples 4 to 7]
Various diamines in the blending amounts shown in Table 1 (linear dimethylpolysiloxane having both molecular chain ends blocked with γ-aminopropyldimethylsiloxy groups: KF-8010 (manufactured by Shin-Etsu Chemical Co., Ltd.), aromatic The first phenolic hydroxyl group according to Synthesis Example 1 except that either or both of diamine: BAPP (2,2-bis [4- (4-aminophenoxy) phenyl] propane) were dissolved in 200 parts of cyclohexanone. A polyamic acid is synthesized with a diamine and an acid anhydride (Synthesis Example 7), and further this is a diamine having a phenolic hydroxyl group (Synthesis Examples 4 and 5 are diamine-1 and Synthesis Example 6 is a phenolic hydroxyl group as a diamine component). Aromatic diamine with amino group bonded to the same aromatic ring: HAB4,4 '-(3,3'-dihydroxy) diaminobiphenyl And a polyamic acid having a phenolic hydroxyl group was synthesized, and a cyclohexanone solution of polyimide resin was obtained in the same manner as in Synthesis Example 1.

[Synthesis Example 8]
Linear dimethyl having both ends of the molecular chain blocked with γ-aminopropyldimethylsiloxy group in a 25 ml moisture meter with a cock connected to a reflux condenser, a thermometer and a 1 L separable flask equipped with a stirrer Polysiloxane: 42.95 parts of KF-8010 (manufactured by Shin-Etsu Chemical Co., Ltd.) and 100 parts of cyclohexanone as a reaction solvent were added and stirred at 80 ° C. to disperse the diamine. By adding dropwise a solution of 37.78 parts of 6FDA (2,2-bis (3,4-dicarboxyphenyl) hexafluoropropane) and 100 parts of cyclohexanone as an acid anhydride and performing a stirring reaction at 80 ° C. for 8 hours, An acid anhydride-rich amic acid oligomer was synthesized.

  Thereafter, 25 ml of toluene was added, the temperature was raised, and the mixture was refluxed at about 160 ° C. for 2 hours. Make sure that a predetermined amount of water has accumulated in the moisture meter and that no water has flowed out. Remove the effluent that has accumulated in the moisture meter and completely remove toluene at 160 ° C. To obtain an acid anhydride-rich imide solution.

  Next, a 25 ml water meter with a cock, a thermometer, and a stirrer in which 19.27 parts of aromatic diamine (diamine-2) having a phenolic hydroxyl group shown below and 100 parts of cyclohexanone are connected to a reflux condenser are connected. Was added to a 1 L separable flask and dispersed, and the imide solution rich in acid anhydride was added dropwise. Thereafter, 25 ml of toluene was added, the temperature was raised, and the mixture was refluxed at about 160 ° C. for 2 hours. Make sure that a predetermined amount of water has accumulated in the moisture meter and that no water has flowed out. Remove the effluent that has accumulated in the moisture meter and completely remove toluene at 160 ° C. Removed. After completion of the reaction, 400 parts of a cyclohexanone solution of a polyimide resin having a phenolic hydroxyl group in the skeleton was obtained. The solvent of the obtained solution was distilled off and then dried under reduced pressure to obtain a polyimide resin.

When the infrared absorption spectrum of the obtained resin was measured, absorption based on polyamic acid indicating that there was an unreacted functional group did not appear, and absorption based on an imide group was confirmed at 1780 cm ⁻¹ and 1720 cm ⁻¹ . Absorption based on a phenolic hydroxyl group was confirmed at 3500 cm ⁻¹ . It was 32000 when the weight average molecular weight (polystyrene conversion) of this resin was measured by the gel permeation chromatography (GPC) which uses tetrahydrofuran as a solvent. The glass transition point determined by thermomechanical measurement was 125 ° C.

[Synthesis Example 9]
In a 1 L separable flask equipped with a 25 ml water meter with a cock connected to a reflux condenser, a thermometer, and a stirrer, 44.00 parts of diaminosiloxane: KF-8010 (manufactured by Shin-Etsu Chemical Co., Ltd.), As a reaction solvent, 100 parts of cyclohexanone was added and stirred at 80 ° C. to disperse the diamine. By adding dropwise a solution of 38.70 parts of 6FDA (2,2-bis (3,4-dicarboxyphenyl) hexafluoropropane) and 100 parts of cyclohexanone as an acid anhydride and performing a stirring reaction at 80 ° C. for 8 hours, An acid anhydride-rich amic acid oligomer was synthesized.

  Thereafter, 25 ml of toluene was added, the temperature was raised, and the mixture was refluxed at about 160 ° C. for 2 hours. Make sure that a predetermined amount of water has accumulated in the moisture meter and that no water has flowed out. Remove the effluent that has accumulated in the moisture meter and completely remove toluene at 160 ° C. To obtain an acid anhydride-rich imide solution.

  Next, a 25 ml water quantitative receiver, thermometer, and stirrer with a cock in which 17.30 parts of aromatic diamine (diamine-3) having a phenolic hydroxyl group shown below and 100 parts of cyclohexanone are connected to a reflux condenser. Was added to a 1 L separable flask and dispersed, and the imide solution rich in acid anhydride was added dropwise. Thereafter, 25 ml of toluene was added, the temperature was raised, and the mixture was refluxed at about 160 ° C. for 2 hours. Make sure that a predetermined amount of water has accumulated in the moisture meter and that no water has flowed out. Remove the effluent that has accumulated in the moisture meter and completely remove toluene at 160 ° C. Removed. After completion of the reaction, 400 parts of a cyclohexanone solution of a polyimide resin having a phenolic hydroxyl group in the skeleton was obtained. The solvent of the obtained solution was distilled off and then dried under reduced pressure to obtain a polyimide resin.

When the infrared absorption spectrum of the obtained resin was measured, absorption based on polyamic acid indicating that there was an unreacted functional group did not appear, and absorption based on an imide group was confirmed at 1780 cm ⁻¹ and 1720 cm ⁻¹ . Absorption based on a phenolic hydroxyl group was confirmed at 3500 cm ⁻¹ . It was 31000 when the weight average molecular weight (polystyrene conversion) of this resin was measured by the gel permeation chromatography (GPC) which uses tetrahydrofuran as a solvent. The glass transition point determined by thermomechanical measurement was 115 ° C.

[Synthesis Example 10]
In a 1 L separable flask equipped with a 25 ml water quantitative receiver with a cock connected to a reflux condenser, a thermometer, and a stirrer, 43.07 parts of diaminosiloxane: KF-8010 (manufactured by Shin-Etsu Chemical Co., Ltd.), As a reaction solvent, 100 parts of cyclohexanone was added and stirred at 80 ° C. to disperse the diamine. By adding dropwise a solution of 37.88 parts of 6FDA (2,2-bis (3,4-dicarboxyphenyl) hexafluoropropane) and 100 parts of cyclohexanone as an acid anhydride and performing a stirring reaction at 80 ° C. for 8 hours, An acid anhydride-rich amic acid oligomer was synthesized.

  Thereafter, 25 ml of toluene was added, the temperature was raised, and the mixture was refluxed at about 160 ° C. for 2 hours. Make sure that a predetermined amount of water has accumulated in the moisture meter and that no water has flowed out. Remove the effluent that has accumulated in the moisture meter and completely remove toluene at 160 ° C. To obtain an acid anhydride-rich imide solution.

  Next, a 25 ml water quantitative receiver, thermometer, and stirrer with a cock, in which 19.05 parts of aromatic diamine (diamine-4) having a phenolic hydroxyl group shown below and 100 parts of cyclohexanone are connected to a reflux condenser Was added to a 1 L separable flask and dispersed, and the imide solution rich in acid anhydride was added dropwise. Thereafter, 25 ml of toluene was added, the temperature was raised, and the mixture was refluxed at about 160 ° C. for 2 hours. Make sure that a predetermined amount of water has accumulated in the moisture meter and that no water has flowed out. Remove the effluent that has accumulated in the moisture meter and completely remove toluene at 160 ° C. Removed. After completion of the reaction, 400 parts of a cyclohexanone solution of a polyimide resin having a phenolic hydroxyl group in the skeleton was obtained. The solvent of the obtained solution was distilled off and then dried under reduced pressure to obtain a polyimide resin.

When the infrared absorption spectrum of the obtained resin was measured, absorption based on polyamic acid indicating that there was an unreacted functional group did not appear, and absorption based on an imide group was confirmed at 1780 cm ⁻¹ and 1720 cm ⁻¹ . Absorption based on a phenolic hydroxyl group was confirmed at 3500 cm ⁻¹ . It was 31000 when the weight average molecular weight (polystyrene conversion) of this resin was measured by the gel permeation chromatography (GPC) which uses tetrahydrofuran as a solvent. The glass transition point determined by thermomechanical measurement was 115 ° C.

In addition, the preparation methods of a polyimide test piece, the glass transition point, and the measuring methods of Young's modulus are as follows.
[Polyimide test piece preparation method]
The polyimide test piece of the present invention was produced as follows. First, a support such as an organic separator or a metal foil was prepared. A cyclohexanone solution of the polyimide heat-resistant resin obtained in Synthesis Examples 1 to 10 was prepared, and the solution was coated on the support by a casting method or the like so that the film thickness after drying was 50 μm. This was dried at 80 ° C. for 30 minutes. The obtained test piece film was peeled off from a support such as an organic separator or metal foil, fixed to a stainless steel frame, heat-treated at 175 ° C. for 1 hour, and dried and cured. Then, the target polyimide heat-resistant resin film was obtained by removing the said support body by peeling, etching, etc.

[Glass transition point]
Using the cyclohexanone solution of the heat resistant resin composition obtained in Synthesis Examples 1 to 10, it was prepared by the above-described test piece preparation method. The prepared test piece was fixed to a stainless steel frame, heat-treated at 175 ° C. for 1 hour, and dried and cured. The glass transition point was measured for a test piece of 20 mm × 5 mm × 50 μm. For the measurement, TMA-2000 (manufactured by ULVAC-RIKO), a measuring device for thermomechanical properties, was used under the conditions of tension mode, distance between chucks of 15 mm, measuring temperature of 25 to 300 ° C., heating rate of 10 ° C./min, and measuring load of 10 g. The glass transition point was measured.

[Young's modulus]
Using the cyclohexanone solution of the heat resistant resin composition obtained in Synthesis Examples 1 to 10, it was prepared by the above-described test piece preparation method. The prepared test piece was fixed to a stainless steel frame, heat-treated at 175 ° C. for 1 hour, and dried and cured. The dynamic viscoelastic modulus was measured for a test piece of 20 mm × 5 mm × 50 μm. The measurement was performed using a dynamic viscoelasticity measuring device, and the Young's modulus at 25 ° C. was measured under the conditions of tension mode, distance between chucks of 15 mm, measurement temperature of 20 to 300 ° C., temperature increase rate of 5 ° C./min, measurement frequency of 30 Hz. .

[Example 1]
As shown in Table 2, 62.93 parts of orthocresol novolac epoxy resin: EOCN1020 (manufactured by Nippon Kayaku Co., Ltd., 220 g / Eq), as shown in Table 2, were added to 20 parts of the cyclohexanone solution of polyimide obtained in Synthesis Example 1. 07 parts of phenol novolak: TD2131 (manufactured by Dainippon Ink, 110 g / Eq), 1 part of tertiary phosphorus catalyst: TPP (manufactured by Hokuko Chemical Co., Ltd.) and 295 so that the solid weight% is 25% After adding 0.000 part of cyclohexanone, the mixture was stirred to obtain a heat resistant resin composition. Next, the glass transition point, Young's modulus, copper polyimide adhesive strength, and 5% weight loss temperature were measured by the following method. The results are also shown in Table 2.

[Examples 2 to 9]
Orthocresol novolak type epoxy resin: EOCN1020, phenol novolac resin at a mixing ratio as shown in Table 2 in the cyclohexanone solution of polyimide obtained in Synthesis Examples 1, 2, 4, 5, 8, 9, 10. TD2131, tertiary phosphorus-based curing catalyst and cyclohexanone were added and stirred to obtain a polyimide resin composition, which was subjected to the same experiment. The results are also shown in Table 2.

[Comparative Examples 1 to 7]
Orthocresol novolac epoxy resin: EOCN1020, phenol novolac resin: TD2131, tertiary phosphorus-based curing catalyst at a blending ratio shown in Table 3 in the cyclohexanone solution of polyimide obtained in Synthesis Examples 3, 6, and 7. Then, after adding cyclohexanone, the mixture was stirred to obtain a heat resistant resin composition, which was subjected to the same experiment. The results are also shown in Table 3.

[Polyimide resin composition test piece preparation method]
The polyimide resin composition test piece of the present invention was produced as follows. First, a support such as an organic separator or a metal foil was prepared. A cyclohexanone solution of the polyimide resin composition test pieces obtained in Examples 1 to 9 and Comparative Examples 1 to 7 was prepared, and the solution was cast on the support so that the film thickness after drying was 50 μm. It was coated by the method. This was dried at 80 ° C. for 30 minutes. The obtained adhesive film was peeled off from a support such as an organic separator or metal foil, fixed to a stainless steel frame, heat-treated at 175 ° C. for 1 hour, and dried and cured. Thereafter, the support was removed by peeling, etching, or the like to obtain a target polyimide resin composition test piece.

[Glass transition point]
The polyimide resin composition test pieces obtained in Examples 1 to 9 and Comparative Examples 1 to 7 were produced by the method described above. The obtained polyimide resin composition test piece was fixed to a stainless steel frame and heat-treated at 175 ° C. for 1 hour to be cured. The glass transition point was measured for a test piece of 20 mm × 5 mm × 50 μm. For the measurement, TMA-2000 (manufactured by ULVAC-RIKO), a measuring device for thermomechanical properties, was used under the conditions of tension mode, distance between chucks of 15 mm, measuring temperature of 25 to 300 ° C., heating rate of 10 ° C./min, and measuring load of 10 g. The glass transition point was measured.

[Young's modulus]
The polyimide resin composition test pieces obtained in Examples 1 to 9 and Comparative Examples 1 to 7 were produced by the method described above. The obtained polyimide resin composition test piece was fixed to a stainless steel frame and heat-treated at 175 ° C. for 1 hour to be cured. The dynamic viscoelastic modulus was measured for a test piece of 20 mm × 5 mm × 50 μm. The measurement was performed using a dynamic viscoelasticity measuring device, and the Young's modulus at 25 ° C. was measured under the conditions of tension mode, distance between chucks of 15 mm, measurement temperature of 20 to 300 ° C., temperature increase rate of 5 ° C./min, measurement frequency of 30 Hz. .

[Adhesive strength]
The polyimide resin composition varnishes obtained in Examples 1 to 9 and Comparative Examples 1 to 7 were bonded to each other with a 18 mm × 18 mm 42-mm Teflon (registered trademark) film having a hole of 5 mm × 5 mm. It was applied on an alloy plate. This was dried in an air stream at 80 ° C. for 30 minutes to remove the solvent. In the following experiment, KAKU-4242 alloy manufactured by Toppan Printing Co., Ltd. was used as a test piece. The sample was sandwiched between 42 alloy test pieces coated with the polyimide resin composition described above and pressed at 150 ° C., 6 kgf / cm ² , for 1 minute. The pressure-bonded laminate was heated at 80 ° C. for 1 hour, 150 ° C. for 1 hour, and 200 ° C. for 1 hour in a nitrogen stream to cure the polyimide resin composition layer to produce an adhesive test piece. Thereafter, using a Shimadzu autograph tensile tester, the shear adhesive strength was measured at a speed of 2.0 mm / min.

[Adhesive strength after PCT]
The polyimide resin composition varnishes obtained in Examples 1 to 9 and Comparative Examples 1 to 7 were bonded to each other with a 18 mm × 18 mm 42-mm Teflon (registered trademark) film having a hole of 5 mm × 5 mm. It was applied on an alloy plate. This was dried in an air stream at 80 ° C. for 30 minutes to remove the solvent. In the following experiment, KAKU-42 42 alloy manufactured by Toppan Printing Co., Ltd. was used as a test piece. The sample was sandwiched between 42 alloy test pieces coated with the polyimide resin composition described above and pressed at 150 ° C., 6 kgf / cm ² , for 1 minute. The pressure-bonded laminate was heated at 80 ° C. for 1 hour, 150 ° C. for 1 hour, and 200 ° C. for 1 hour in a nitrogen stream to cure the polyimide resin composition layer to produce an adhesive test piece. After holding the above-mentioned test piece for 24 hours under PCT conditions, the shear adhesive force was measured at a speed of 2.0 mm / min using an autograph tensile tester manufactured by Shimadzu Corporation.

Claims (6)

A skeleton having a repeating unit represented by the following structural formulas (1) and (2) and produced using a diamine having a phenolic hydroxyl group on an aromatic ring different from the aromatic ring to which an amino group is bonded as a diamine Polyimide resin having a phenolic hydroxyl group inside.

Wherein X is one or more tetravalent organic groups selected from the following group [I], and Y is a diamine residue Y ₁ having a phenolic hydroxyl group represented by the following formula [II]. A divalent organic group, Z is a siloxane diamine residue represented by the following formula [IV], m and n are natural numbers, m / (m + n) is 0.1 to 0.99, and 10 ≦ m + n ≦ 500.

(R independently represents a hydrogen atom, a halogen atom, or a substituted or unsubstituted monovalent hydrocarbon group having 1 to 8 carbon atoms.)

(A is a group selected from the following group [IIa], B is a group selected from the following group [IIb],

, R has the same meaning as described above, and k is a natural number of 1 to 5. )

(R ¹ independently represents an alkylene group or arylene group having 1 to 8 carbon atoms, R ² independently represents an alkyl group, alkoxy group or aryl group having 1 to 8 carbon atoms, and j represents an integer of 4 to 60. Shown]]] A skeleton having a repeating unit represented by the following structural formulas (1) and (2) and produced using a diamine having a phenolic hydroxyl group on an aromatic ring different from the aromatic ring to which an amino group is bonded as a diamine Polyimide resin having a phenolic hydroxyl group inside.

[Wherein X is one or more tetravalent organic groups selected from the following group [I], Y is a diamine residue Y ₁ having a phenolic hydroxyl group represented by the following formula [II], and A divalent organic group consisting of an aromatic diamine residue Y ₂ selected from the following group [III], Z is a siloxane diamine residue represented by the following formula [IV], and Y ₁ / (Y ₁ + Y ₂ ) Is a molar ratio of 0.01 to 1, m and n are natural numbers, m / (m + n) is 0.1 to 0.99, and 10 ≦ m + n ≦ 500.

(R independently represents a hydrogen atom, a halogen atom, or a substituted or unsubstituted monovalent hydrocarbon group having 1 to 8 carbon atoms.)

(A is a group selected from the following group [IIa ′], B is a group selected from the following group [IIb],

, R has the same meaning as described above, and k is a natural number of 1 to 5. )

(R has the same meaning as above.)

(R ¹ independently represents an alkylene group or arylene group having 1 to 8 carbon atoms, R ² independently represents an alkyl group, alkoxy group or aryl group having 1 to 8 carbon atoms, and j represents an integer of 4 to 60. Shown]]] A skeleton having a repeating unit represented by the following structural formulas (1) and (2) and produced using a diamine having a phenolic hydroxyl group on an aromatic ring different from the aromatic ring to which an amino group is bonded as a diamine Polyimide resin having a phenolic hydroxyl group inside.

[Wherein X is one or more tetravalent organic groups selected from the following group [I], Y is a diamine residue Y ₁ having a phenolic hydroxyl group represented by the following formula [II], and A divalent organic group consisting of an aromatic diamine residue Y ₂ selected from the following group [III], Z is a siloxane diamine residue represented by the following formula [IV], and Y ₁ / (Y ₁ + Y ₂ ) Is a molar ratio of 0.01 to 1, m and n are natural numbers, m / (m + n) is 0.1 to 0.99, and 10 ≦ m + n ≦ 500.

(R independently represents a hydrogen atom, a halogen atom, or a substituted or unsubstituted monovalent hydrocarbon group having 1 to 8 carbon atoms.)

(A is a group selected from the following group [IIa], B is a group selected from the following group [IIb ′],

, R has the same meaning as described above, and k is a natural number of 1 to 5. )

(R has the same meaning as above.)

(R ¹ independently represents an alkylene group or arylene group having 1 to 8 carbon atoms, R ² independently represents an alkyl group, alkoxy group or aryl group having 1 to 8 carbon atoms, and j represents an integer of 4 to 60. Shown]]]   The polyimide resin composition containing the polyimide resin of any one of Claims 1 thru | or 3.   Furthermore, the polyimide resin composition of Claim 4 containing the epoxy resin which has a 2 or more glycidyl group.   Furthermore, the polyimide resin composition of Claim 5 containing an epoxy resin hardening | curing agent.