JP7523967B2 - Modified siloxane diamine compound and polyimide resin - Google Patents

Description

This invention relates to modified siloxane diamine compounds and polyimide resins.

Polyimide resins are materials that are widely used in the electronics field, and many polyimide resins that have siloxane structures in the molecule have been proposed to give the resin flexibility, as described in Patent Document 1. However, the siloxane diamine compounds used in the synthesis have low purity, and low molecular weight siloxanes volatilize at high temperatures, causing problems such as poor bonding in electrical wiring and poor adhesion to various substrates.

JP 2005-056921 A

The present invention aims to provide an organically modified siloxane diamine compound and a polyimide resin with excellent adhesion obtained by using the same.

As a result of extensive research to achieve the above object, it was discovered that an organically modified siloxane diamine compound and a polyimide resin obtained using the same have flexibility and excellent adhesion. The present invention comprises the following:

[1]. A modified siloxane diamine compound having an amino group at the end and represented by the following structure.

(In the above chemical formula, G is an organic group having 1 to 50 carbon atoms in the main chain and containing one or more of the following atoms: H atom, O atom, N atom, halogen atom, or S atom; X is an organic group having an amino group in its structure; R is an organic group having 1 to 20 carbon atoms; n is an integer from 0 to 50; and m is an integer from 1 to 50.)

[2]. The modified siloxane diamine compound according to claim 1, obtained by reacting (A) a compound having two carbon-carbon double bonds in one molecule, (B) a silicon compound having two SiH groups in one molecule, and (C) a compound having one carbon-carbon double bond and one amino group in one molecule.

[3]. The modified siloxane diamine compound according to claim 2, characterized in that component (C) is allylamine or an inorganic salt of allylamine.

[4]. The modified siloxane diamine compound according to [2] or [3], characterized in that component (A) is a compound represented by the following general formula (a):

(wherein R represents a hydrogen atom or a monovalent organic group having 1 to 50 carbon atoms).
[5] A polyimide resin which is a reaction product of the modified siloxane diamine compound according to any one of [1] to [4] with a diacid anhydride compound.

The present invention provides an organically modified siloxane diamine compound and a polyimide resin obtained using the same that has excellent adhesion.

(Modified siloxane diamine compound)
The modified siloxane diamine compound is a modified siloxane diamine compound having an amino group at its terminal and represented by the following structure.

(In the above chemical formula, G is an organic group having 1 to 50 carbon atoms in the main chain and containing one or more of the following atoms: H atom, O atom, N atom, halogen atom, or S atom; X is an organic group having an amino group in its structure; R is an organic group having 1 to 20 carbon atoms; n is an integer from 0 to 50; and m is an integer from 1 to 50.)

The structure G referred to here indicates an organic group consisting of 1 to 50 carbon atoms and any of the following atoms: H, O, N, F, or S. In the polyimide resin obtained by the present invention, the method of introduction using the hydrosilylation reaction shown below is preferable, since it is effective in improving adhesion to the substrate and resin strength compared to a resin having a siloxane molecule that does not have structure G, and it can be introduced without impairing the heat resistance that is a characteristic of polyimide resins.

Below, we explain each of the essential components required to obtain a modified siloxane diamine compound using a hydrosilylation reaction.

(Component (A): a compound having two carbon-carbon double bonds in one molecule)
The modified siloxane diamine compound can be obtained by reacting a compound having two carbon-carbon double bonds in one molecule of component (A) with components (B) and (C) described below. There are no particular limitations on the compound as long as it is a compound having two carbon-carbon double bonds in one molecule of component (A) in the present invention.

The carbon-carbon double bond of component (A) is not particularly limited, but may be represented by the following general formula (b):

(wherein ^R4 represents a hydrogen atom or a methyl group) is preferred from the viewpoint of reactivity. Also, from the viewpoint of availability of raw materials,

The group represented by is particularly preferred.

As the carbon-carbon double bond of component (A), an alicyclic group having a partial structure represented by the following general formula (c) in the ring is preferred because it provides high heat resistance to the cured product.

(In the formula, R ⁵ represents a hydrogen atom or a methyl group.) From the viewpoint of availability of raw materials, an alicyclic group having a partial structure represented by the following formula within the ring is preferred.

The carbon-carbon double bond may be directly bonded to the skeleton of component (A) or may be covalently bonded via a divalent or higher substituent. The divalent or higher substituent is not particularly limited as long as it is a substituent having 0 to 10 carbon atoms, but is preferably one containing only C, H, N, O, S, and halogen as constituent elements. Examples of these substituents include:

and the like. Two or more of these divalent or more substituents may be linked by a covalent bond to form one divalent or more substituent.

Examples of groups that are covalently bonded to the above-mentioned skeletal portions include vinyl groups, allyl groups, methallyl groups, acrylic groups, methacrylic groups, 2-hydroxy-3-(allyloxy)propyl groups, 2-allylphenyl groups, 3-allylphenyl groups, 4-allylphenyl groups, 2-(allyloxy)phenyl groups, 3-(allyloxy)phenyl groups, 4-(allyloxy)phenyl groups, 2-(allyloxy)ethyl groups, 2,2-bis(allyloxymethyl)butyl groups, 3-allyloxy-2,2-bis(allyloxymethyl)propyl groups, vinyl ether groups, and the like.

Specific examples of component (A) include diallyl phthalate, diethylene glycol bisallyl carbonate, trimethylolpropane diallyl ether, diarylidene pentaerythritol, and diallyl monomethyl isocyanurate. Diallyl monopropyl isocyanurate, diallyl monoglycidyl isocyanurate, diallyl monobenzyl isocyanurate, diallyl dimethyl glycoluril, 1,4-butanediol divinyl ether, nonanediol divinyl ether, 1,4-cyclohexane dimethanol divinyl ether, triethylene glycol divinyl ether, diallyl ether of bisphenol S, divinylbenzene, divinyl biphenyl, 1,3-diisopropenylbenzene, 1,4-diisopropenylbenzene, 1,3-bis(allyloxy)adamantane, 1,3-bis(vinyloxy)adamantane, dicyclopentadiene, vinylcyclohexene, 1,5-hexadiene, 1,9-decadiene, diallyl ether, bisphenol A diallyl ether, tetraallyl bisphenol A, 2,5-diallylphenol allyl ether

These include:

As component (A), from the viewpoint of low coloration of the resulting cured product and high heat resistance, diallyl monomethyl isocyanurate, diallyl monopropyl isocyanurate, diallyl monoglycidyl isocyanurate, diallyl monobenzyl isocyanurate, vinylcyclohexene, dicyclopentadiene, and diallyl ether of 2,2-bis(4-hydroxycyclohexyl)propane are preferred.

In particular, from the viewpoint of high heat resistance and light resistance, diallyl monomethyl isocyanurate, diallyl monopropyl isocyanurate, and derivatives thereof represented by the following general formula (a) are preferred.

(In the formula, R represents a hydrogen atom or a monovalent organic group having 1 to 50 carbon atoms)

Silicon-based compounds having two carbon-carbon double bonds can also be used. The most commonly available are linear polysiloxanes terminated with vinyl groups, but there are no particular limitations on the polyorganosiloxane polymers, so long as they are homopolymers of dimethylsiloxane units, diphenylsiloxane units, and methylphenylsiloxane units, and copolymers of each siloxane unit, and the polyorganosiloxane polymers are end-blocked with dimethylvinylsilyl groups. Specific examples of preferred compounds include 1,1,3,3-tetramethyldivinyldisiloxane, 1,1,3,3,5,5-hexamethyldivinyltrisiloxane, and 1,1,5,5-tetramethyldivinyl-3,3-diphenyltrisiloxane. Silicon-based compounds other than vinyl-terminated polysiloxane compounds can also be used, such as 1,4-bis(dimethylvinylsilyl)benzene, 1,4-bis(diphenylvinylsilyl)benzene, 1,4-bis(methylphenylvinylsilyl)benzene, divinyldimethylsilane, divinylcyclohexylmethylsilane, divinylphenylmethylsilane, divinyldicyclohexylsilane, divinyldiphenylsilane, bis(vinyldimethylsilyl)methane, bis(vinylphenylmethylsilyl)methane, bis(vinylcyclohexylmethylsilyl)methane, bis(vinyldiphenylsilyl)methane, (vinyldimethylsilyl)(divinylmethylsilyl)methane, (vinylphenylmethylsilyl)(divinylmethylsilyl)methane, 1,2-bis(vinyldimethylsilyl)ethane, 1,2- Bis(vinyldiphenylsilyl)ethane, 1,2-bis(divinylmethylsilyl)ethane, 1,2-bis(divinylphenylsilyl)ethane, 1,3-bis(vinyldimethylsilyl)propane, 1,3-bis(vinyldiphenylsilyl)propane, 1,4-bis(vinyldimethylsilyl)butane, 1,4-bis(vinyldiphenylsilyl)butane, 1,5-bis(vinyldimethylsilyl)pentane, 1,5-bis(vinyldiphenylsilyl)pentane, 1,4-bis(vinyldimethylsilyl)cyclohexane, 1,4-bis(vinylphenylmethylsilyl)cyclohexane, 1,4-bis(vinylcyclohexylmethylsilyl)cyclohexane, 1,4-bis(vinyldiphenylsilyl)cyclohexane, 1,3-bis(vinylphenylmethylsilyl)cyclohexane, 1,3-bis(vinylcyclohexylmethylsilyl)cyclohexane, 1,3-bis(vinyldiphenylsilyl)cyclohexane, 1,3-bis(vinyldimethylsilyl)cyclohexane, 1,4-bis(vinylphenylmethylsilyl)benzene, 1,4-bis(vinylcyclohexylmethylsilyl)benzene, 1,4-bis(vinyldiphenylsilyl)benzene, 1,4-bis(divinylmethylsilyl)benzene, 1,3-bis(vinyldimethylsilyl)benzene, 1,3-bis(vinylphenylmethylsilyl)benzene, 1,3-bis(vinylcyclohexylmethylsilyl)benzene, 1,3-bis(vinyldiphenylsilyl)benzene, 2,6-bis(vinyldimethylsilyl)naphthalene, 2,6-bis(vinylphenylmethylsilyl)naphthalene, 2,6-bis(vinylcyclohexylmethylsilyl)naphthalene, 2, Examples include 6-bis(vinyldiphenylsilyl)naphthalene, 2,7-bis(vinyldimethylsilyl)naphthalene, 2,7-bis(vinylphenylmethylsilyl)naphthalene, 2,7-bis(vinylcyclohexylmethylsilyl)naphthalene, 2,7-bis(vinyldiphenylsilyl)naphthalene, 2,7-bis(vinyldimethylsilyl)anthracene, 2,7-bis(vinylphenylmethylsilyl)anthracene, 2,7-bis(vinylcyclohexylmethylsilyl)anthracene, 2,7-bis(vinyldiphenylsilyl)anthracene, 2,8-bis(vinyldimethylsilyl)anthracene, 2,8-bis(vinylphenylmethylsilyl)anthracene, 2,8-bis(vinylcyclohexylmethylsilyl)anthracene, and 2,8-bis(vinyldiphenylsilyl)anthracene.

(Component (B): Silicon compound having two SiH groups in one molecule)
As component (B), any silicon compound having two SiH groups, that is, any compound having two SiH groups each having a Si atom in the molecule, can be used without any particular limitation. The most commonly available one is a linear polysiloxane having a SiH group terminal, but there is no particular limitation as long as it is a homopolymer of dimethylsiloxane units, diphenylsiloxane units, or methylphenylsiloxane units, or a polyorganosiloxane polymer in which the terminals of each copolymer of siloxane units are blocked with dimethylhydrogensilyl groups. Specifically, for example, 1,1,3,3-tetramethyldisiloxane, 1,1,3,3,5,5-hexamethyltrisiloxane, 1,1,5,5-tetramethyl-3,3-diphenyltrisiloxane, etc. are exemplified as preferred examples. Furthermore, silicon-based compounds other than polysiloxane compounds having SiH groups at their ends can also be used. Specific examples of such compounds include 1,4-bis(dimethylsilyl)benzene, 1,4-bis(diphenylsilyl)benzene, and 1,4-bis(methylphenylsilyl)benzene.

(Component (C): A compound having one carbon-carbon double bond and one amino group per molecule)
As component (C), any compound having one carbon-carbon double bond and one amino group per molecule can be used without any particular limitation. Specific examples include allylamine, allylamine hydrochloride, 2-methylallylamine hydrochloride, 4-aminostyrene, vinylamine, and ethynylamine. From the viewpoints of reactivity and toxicity, allylamine hydrochloride is preferred.

(Reaction of Components (A), (B), and (C))
The method for reacting components (A), (B), and (C) to obtain a modified siloxane diamine compound is a hydrosilylation reaction, in which a catalyst may be used to facilitate the reaction.

As the catalyst for the hydrosilylation reaction, for example, the following can be used: Platinum alone, solid platinum supported on a support such as alumina, silica, or carbon black, chloroplatinic acid, complexes of chloroplatinic acid with alcohols, aldehydes, ketones, etc., platinum-olefin complexes (e.g., Pt(CH ₂ ═CH ₂ ) ₂ (PPh ₃ ) ₂ , Pt(CH ₂ ═CH ₂ ) ₂ Cl ₂ ), platinum-vinylsiloxane complexes (e.g., Pt(ViMe ₂ SiOSiMe ₂ Vi) _n , Pt[(MeViSiO) ₄ ] _m ), platinum-phosphine complexes (e.g., Pt(PPh ₃ ) ₄ , Pt(PBu ₃ ) ₄ ), platinum-phosphite complexes (e.g., Pt[P(OPh) ₃ ] ₄ , Pt[P(OBu) ₃ ] ₄ ) (wherein Me is a methyl group, Bu is a butyl group, Vi is a vinyl group, Ph is a phenyl group, and n and m are integers), dicarbonyldichloroplatinum, Karstedt's catalyst, and also the platinum-hydrocarbon complexes described in U.S. Pat. Nos. 3,159,601 and 3,159,662 to Ashby, and the platinum alcoholate catalysts described in U.S. Pat. No. 3,220,972 to Lamoreaux. Additionally, platinum chloride-olefin complexes described in U.S. Pat. No. 3,516,946 to Modic are also useful in the present invention.

Examples _of catalysts other than platinum compounds include RhCl(PPh) ₃ , _RhCl3 , _RhAl2O3 , _RuCl3 , _IrCl3 , _FeCl3 , _{AlCl3 , PdCl2.2H2O} , _NiCl2 , _TiCl4 , and the like.

Among these, chloroplatinic acid, platinum-olefin complexes, platinum-vinylsiloxane complexes, etc. are preferred from the viewpoint of catalytic activity. These catalysts may be used alone or in combination of two or more kinds.

Regarding the order of reaction of components (A), (B), and (C), first, components (A) and (B) are reacted by hydrosilylation under conditions that increase the amount of SiH groups, and then component (C) is reacted successively to introduce amino groups to the terminals, thereby obtaining a modified siloxane diamine compound.

(Regarding polyimide resin)
The polyimide resin obtained by using the modified siloxane diamine compound of the present invention is generally obtained by reaction with a diacid anhydride, and is not particularly limited.

Examples of diacid anhydrides used in the synthesis of the polyimide of the present invention include 2,2'-hexafluoropropylidenediphthalic dianhydride, 2,2-bis(4-hydroxyphenyl)propane dibenzoate-3,3',4,4'-tetracarboxylic dianhydride, butane tetracarboxylic dianhydride, 1,2,3,4-cyclobutane tetracarboxylic dianhydride, 1,3-dimethyl-1,2,3,4-cyclobutane tetracarboxylic acid, 1,2,3,4-cyclopentane tetracarboxylic dianhydride, 2,3,5-tricarboxycyclopentylacetic dianhydride, and 3,5,6-tricarboxynorbonane-2-acetic acid. dianhydrides, aliphatic or alicyclic tetracarboxylic dianhydrides such as 2,3,4,5-tetrahydrofuran tetracarboxylic dianhydride, 5-(2,5-dioxotetrahydrofuryl)-3-methyl-3-cyclohexene-1,2-dicarboxylic dianhydride, and bicyclo[2,2,2]-oct-7-ene-2,3,5,6-tetracarboxylic dianhydride, pyromellitic dianhydride, 3,3',4,4'-benzophenone tetracarboxylic dianhydride, 3,3',4,4'-biphenylsulfone tetracarboxylic dianhydride, 1,4,5,8-naphthalene tetracarboxylic dianhydride, and 2,3,6,7-naphthalene tetracarboxylic dianhydride. dianhydride, 3,3',4,4'-biphenyl ether tetracarboxylic acid dianhydride, 3,3',4,4'-dimethyldiphenylsilane tetracarboxylic acid dianhydride, 3,3',4,4'-tetraphenylsilane tetracarboxylic acid dianhydride, 1,2,3,4-furan tetracarboxylic acid dianhydride, 4,4'-bis(3,4-dicarboxyphenoxy)diphenyl sulfide dianhydride, 4,4'-bis(3,4-dicarboxyphenoxy)diphenyl sulfone dianhydride, 4,4'-bis(3,4-dicarboxyphenoxy)diphenylpropane dianhydride, 3,3',4,4'-perfluoroisopropyl ether dianhydride, Examples of the aromatic tetracarboxylic acid dianhydrides include isopropylidenediphthalic dianhydride, 3,3',4,4'-biphenyltetracarboxylic dianhydride, bis(phthalic acid)phenylphosphine oxide dianhydride, p-phenylene-bis(triphenylphthalic acid) dianhydride, m-phenylene-bis(triphenylphthalic acid) dianhydride, bis(triphenylphthalic acid)-4,4'-diphenyl ether dianhydride, and bis(triphenylphthalic acid)-4,4'-diphenylmethane dianhydride, and derivatives thereof. These can be used alone or as a mixture of any ratio.

The present invention will be described in more detail below with reference to examples, but the present invention is not limited to the following examples.

(Adhesion Evaluation)
The polyimide resin solutions obtained in the examples and comparative examples were spin-coated on a Cu film-formed wafer substrate to a thickness of 5 μm, and then heated on a hot plate at 250° C. for 1 hour to form a polyimide resin film. Next, a cross-cut test was performed in accordance with JIS K5600-V-VI (ISO2409) to evaluate the adhesion to the Cu thin film.

●Evaluation index 0: No peeling 1: 1-10% peeling 2: 20-30% peeling 3: 50% peeling 4: 70-80% peeling 5: 90% or more peeling

(Heat resistance evaluation)
Using a thermogravimetric analyzer (TGA, manufactured by Shimadzu Corporation), the temperature was raised from room temperature to 500° C. at a rate of 10° C./min, and evaluation was performed using the 1% weight loss temperature as an index.

Example 1
A 500 mL four-neck flask was charged with 100 g of toluene and 15 g of 1,1,5,5-tetramethyl-3,3-diphenyltrisiloxane, and the gas phase was replaced with nitrogen, and then the mixture was heated and stirred at an internal temperature of 105°C. A mixture of 9 g of diallyl monomethyl isocyanurate, 10 g of toluene, and 0.0163 g of a xylene solution of platinum vinyl siloxane complex (containing 3 wt% platinum) was added dropwise over 30 minutes. Three hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the allyl group was 100%, and the mixture was cooled to 60°C. Then, a mixture of 0.85 g of allylamine hydrochloride and 3 g of 1,4-dioxane was added dropwise. Five hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the double bond of allylamine was 100%, and the reaction was terminated by cooling. The toluene was distilled off under reduced pressure to obtain a modified siloxane compound A having an amino group at the terminal.

Next, 20 g of N,N-dimethylformamide as a solvent, 2.5 g of the modified siloxane compound A obtained above, and 1.4 g of 4,4'-oxydiphthalic anhydride were added to a 200 mL flask and stirred at room temperature under a nitrogen atmosphere for 30 minutes. 5 g of N,N-dimethylformamide, 0.8 g of pyridine, and 1.5 g of acetic anhydride were added to the flask in that order and stirred for 3 hours while heating to 90°C. After returning to room temperature, 500 mL of isopropyl alcohol was added to the flask and the precipitate was collected. The mixture was washed three times with 500 mL of isopropyl alcohol, and the obtained precipitate was dried under reduced pressure at 80°C for 6 hours, and then diluted to 50% with N,N-dimethylformamide to obtain polyimide resin solution A.

Example 2
A 500 mL four-neck flask was charged with 100 g of toluene and 15 g of 1,1,5,5-tetramethyl-3,3-diphenyltrisiloxane, and the gas phase was replaced with nitrogen, and then the mixture was heated and stirred at an internal temperature of 105°C. A mixture of 8 g of diallyl monopropyl isocyanurate, 10 g of toluene, and 0.0163 g of a xylene solution of platinum vinyl siloxane complex (containing 3 wt% platinum) was added dropwise over 30 minutes. Three hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the allyl group was 100%, and the mixture was cooled to 60°C. Then, a mixture of 0.85 g of allylamine hydrochloride and 3 g of 1,4-dioxane was added dropwise. Five hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the double bond of allylamine was 100%, and the reaction was terminated by cooling. The toluene was distilled off under reduced pressure to obtain a modified siloxane compound B having an amino group at the end.

Next, 20 g of N,N-dimethylformamide as a solvent, 2.5 g of the modified siloxane compound B obtained above, and 1.4 g of 4,4'-oxydiphthalic anhydride were added to a 200 mL flask and stirred at room temperature under a nitrogen atmosphere for 30 minutes. 5 g of N,N-dimethylformamide, 0.8 g of pyridine, and 1.5 g of acetic anhydride were added to the flask in that order and stirred for 3 hours while heating to 90°C. After the temperature returned to room temperature, 500 mL of isopropyl alcohol was added to the flask and the precipitate was collected. The mixture was washed three times with 500 mL of isopropyl alcohol, and the obtained precipitate was dried under reduced pressure at 80°C for 6 hours, and then diluted to 50% with N,N-dimethylformamide to obtain polyimide resin solution B.

Example 3
A 500 mL four-neck flask was charged with 100 g of toluene and 15 g of 1,1,5,5-tetramethyl-3,3-diphenyltrisiloxane, and the gas phase was replaced with nitrogen, and then the mixture was heated and stirred at an internal temperature of 105°C. A mixture of 12 g of bis(p-allyloxyphenyl)sulfone, 10 g of toluene, and 0.0163 g of a xylene solution of platinum vinylsiloxane complex (containing 3 wt% platinum) was added dropwise over 30 minutes. Three hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the allyl group was 100%, and the mixture was cooled to 60°C. Then, a mixture of 0.85 g of allylamine hydrochloride and 3 g of 1,4-dioxane was added dropwise. Five hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the double bond of allylamine was 100%, and the reaction was terminated by cooling. The toluene was distilled off under reduced pressure to obtain a modified siloxane compound C having an amino group at its terminal.

Next, 20 g of N,N-dimethylformamide as a solvent, 2.5 g of the modified siloxane compound C obtained above, and 1.4 g of 4,4'-oxydiphthalic anhydride were added to a 200 mL flask and stirred at room temperature under a nitrogen atmosphere for 30 minutes. 5 g of N,N-dimethylformamide, 0.8 g of pyridine, and 1.5 g of acetic anhydride were added to the flask in that order and stirred for 3 hours while heating to 90°C. After returning to room temperature, 500 mL of isopropyl alcohol was added to the flask and the precipitate was collected. The mixture was washed three times with 500 mL of isopropyl alcohol, and the obtained precipitate was dried under reduced pressure at 80°C for 6 hours, and then diluted to 50% with N,N-dimethylformamide to obtain polyimide resin solution C.

Example 4
A 500 mL four-neck flask was charged with 100 g of toluene and 15 g of 1,1,5,5-tetramethyl-3,3-diphenyltrisiloxane, and the gas phase was replaced with nitrogen, and then the mixture was heated and stirred at an internal temperature of 105°C. A mixture of 4 g of divinylbenzene, 10 g of toluene, and 0.0163 g of a xylene solution of platinum vinylsiloxane complex (containing 3 wt% platinum) was added dropwise over 30 minutes. Three hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the allyl group was 100%, and the mixture was cooled to 60°C. Then, a mixture of 0.85 g of allylamine hydrochloride and 3 g of 1,4-dioxane was added dropwise. Five hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the double bond of the allylamine was 100%, and the mixture was cooled to terminate the reaction. The toluene was distilled off under reduced pressure to obtain modified siloxane compound D having an amino group at the end.

Next, 20 g of N,N-dimethylformamide as a solvent, 2.5 g of the modified siloxane compound D obtained above, and 1.4 g of 4,4'-oxydiphthalic anhydride were added to a 200 mL flask and stirred at room temperature for 30 minutes under a nitrogen atmosphere. 5 g of N,N-dimethylformamide, 0.8 g of pyridine, and 1.5 g of acetic anhydride were added to the flask in that order and stirred for 3 hours while heating to 90°C. After the temperature returned to room temperature, 500 mL of isopropyl alcohol was added to the flask and the precipitate was collected. The mixture was washed three times with 500 mL of isopropyl alcohol, and the resulting precipitate was dried under reduced pressure at 80°C for 6 hours, and then diluted to 50% with N,N-dimethylformamide to obtain polyimide resin solution D.

Example 5
A 500 mL four-neck flask was charged with 100 g of toluene and 15 g of 1,1,5,5-tetramethyl-3,3-diphenyltrisiloxane, and the gas phase was replaced with nitrogen, and then the mixture was heated and stirred at an internal temperature of 105°C. A mixture of 12.5 g of vinylnorbornene, 10 g of toluene, and 0.0163 g of a xylene solution of platinum vinylsiloxane complex (containing 3 wt% platinum) was added dropwise over 30 minutes. Three hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the allyl group was 100%, and the mixture was cooled to 60°C. Then, a mixture of 0.85 g of allylamine hydrochloride and 3 g of 1,4-dioxane was added dropwise. Five hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the double bond of allylamine was 100%, and the reaction was terminated by cooling. The toluene was distilled off under reduced pressure to obtain a modified siloxane compound E having an amino group at the end.

Next, 20 g of N,N-dimethylformamide as a solvent, 2.5 g of the modified siloxane compound E obtained above, and 1.4 g of 4,4'-oxydiphthalic anhydride were added to a 200 mL flask and stirred at room temperature under a nitrogen atmosphere for 30 minutes. 5 g of N,N-dimethylformamide, 0.8 g of pyridine, and 1.5 g of acetic anhydride were added to the flask in that order and stirred for 3 hours while heating to 90°C. After the temperature returned to room temperature, 500 mL of isopropyl alcohol was added to the flask and the precipitate was collected. The mixture was washed three times with 500 mL of isopropyl alcohol, and the resulting precipitate was dried under reduced pressure at 80°C for 6 hours, and then diluted to 50% with N,N-dimethylformamide to obtain polyimide resin solution E.

(Example 6)
A 500 mL four-neck flask was charged with 100 g of toluene and 15 g of 1,1,5,5-tetramethyl-3,3-diphenyltrisiloxane, and the gas phase was replaced with nitrogen, and then the mixture was heated and stirred at an internal temperature of 105°C. A mixture of 11 g of 2,2-bis(3-allyl-4-hydroxyphenyl)propane, 10 g of toluene, and 0.0163 g of a xylene solution of platinum vinylsiloxane complex (containing 3 wt% platinum) was added dropwise over 30 minutes. Three hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the allyl group was 100%, and the mixture was cooled to 60°C. Then, a mixture of 0.85 g of allylamine hydrochloride and 3 g of 1,4-dioxane was added dropwise. Five hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the double bond of the allylamine was 100%, and the reaction was terminated by cooling. The toluene was distilled off under reduced pressure to obtain modified siloxane compound F having amino groups at its terminals.

Next, 20 g of N,N-dimethylformamide as a solvent, 2.5 g of the modified siloxane compound F obtained above, and 1.4 g of 4,4'-oxydiphthalic anhydride were added to a 200 mL flask and stirred at room temperature for 30 minutes under a nitrogen atmosphere. 5 g of N,N-dimethylformamide, 0.8 g of pyridine, and 1.5 g of acetic anhydride were added to the flask in that order and stirred for 3 hours while heating to 90°C. After returning to room temperature, 500 mL of isopropyl alcohol was added to the flask and the precipitate was collected. The mixture was washed three times with 500 mL of isopropyl alcohol, and the resulting precipitate was dried under reduced pressure at 80°C for 6 hours, and then diluted to 50% with N,N-dimethylformamide to obtain polyimide resin solution F.

(Example 7)
A 500 mL four-neck flask was charged with 100 g of toluene and 15 g of 1,1,5,5-tetramethyl-3,3-diphenyltrisiloxane, and the gas phase was replaced with nitrogen, and then the flask was heated and stirred at an internal temperature of 105°C. A mixture of 12 g of 1,1,5,5-tetramethyldivinyl-3,3-diphenyltrisiloxane, 10 g of toluene, and 0.0163 g of a xylene solution of platinum vinylsiloxane complex (containing 3 wt% platinum) was added dropwise over 30 minutes. Three hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the allyl group was 100%, and the flask was cooled to 60°C. A mixture of 0.85 g of allylamine hydrochloride and 3 g of 1,4-dioxane was then added dropwise. Five hours after the end of the addition, it was confirmed by ¹ H-NMR that the reaction rate of the double bond of the allylamine was 100%, and the flask was cooled to terminate the reaction. The toluene was distilled off under reduced pressure to obtain a modified siloxane compound G having an amino group at the end.

Next, 20 g of N,N-dimethylformamide as a solvent, 2.5 g of the modified siloxane compound G obtained above, and 1.4 g of 4,4'-oxydiphthalic anhydride were added to a 200 mL flask and stirred at room temperature under a nitrogen atmosphere for 30 minutes. 5 g of N,N-dimethylformamide, 0.8 g of pyridine, and 1.5 g of acetic anhydride were added to the flask in that order and stirred for 3 hours while heating to 90°C. After the temperature returned to room temperature, 500 mL of isopropyl alcohol was added to the flask and the precipitate was collected. The mixture was washed three times with 500 mL of isopropyl alcohol, and the resulting precipitate was dried under reduced pressure at 80°C for 6 hours, and then diluted to 50% with N,N-dimethylformamide to obtain polyimide resin solution G.

(Comparative Example 1)
In a 200 mL flask, 20 g of N,N-dimethylformamide, 1.5 g of siloxane diamine (trade name: KF-8010, manufactured by Shin-Etsu Chemical Co., Ltd.), and 2.5 g of 2,2'-hexafluoropropylidenediphthalic dianhydride were added as a solvent, and the mixture was stirred at room temperature for 30 minutes under a nitrogen atmosphere. Furthermore, 5 g of N,N-dimethylformamide, 0.8 g of pyridine, and 1.5 g of acetic anhydride were sequentially added to the flask, and the mixture was stirred for 3 hours while heating to 90 ° C. After the temperature returned to normal, 500 mL of isopropyl alcohol was added to the flask, and the precipitate was collected. The mixture was further washed three times with 500 mL of isopropyl alcohol, and the obtained precipitate was dried under reduced pressure at 80 ° C. for 6 hours, and then diluted to 50% with N,N-dimethylformamide to obtain polyimide resin solution H.

(Comparative Example 2)
In a 200 mL flask, 20 g of N,N-dimethylformamide, 1.5 g of 2,2-bis(4-aminophenyl)hexafluoropropane, and 2.5 g of 2,2'-hexafluoropropylidenediphthalic dianhydride were added as solvents, and the mixture was stirred at room temperature for 30 minutes under a nitrogen atmosphere. 5 g of N,N-dimethylformamide, 0.8 g of pyridine, and 1.5 g of acetic anhydride were added in sequence to the flask, and the mixture was stirred for 3 hours while heating to 90 ° C. After the mixture returned to room temperature, 500 mL of isopropyl alcohol was added to the flask, and the precipitate was collected. The mixture was washed three times with 500 mL of isopropyl alcohol, and the precipitate was dried under reduced pressure at 80 ° C. for 6 hours, and then diluted to 50% with N,N-dimethylformamide to obtain polyimide resin solution I.

(result)
The above-mentioned evaluations were carried out on the polyimide resin solutions obtained in Examples 1 to 7 and Comparative Examples 1 and 2. The results are shown in Table 1.

The present invention can be used in a variety of fields, such as insulating interlayer films, adhesives, coating agents, and sealants for electronic devices such as semiconductors and displays.

Claims (4)

The compound is obtained by reacting (A) a compound having two carbon-carbon double bonds in one molecule, (B) a silicon compound having two SiH groups in one molecule, and (C) a compound having one carbon-carbon double bond and one amino group in one molecule,
The compound (C) having one carbon-carbon double bond and one amino group per molecule is one or more selected from allylamine, allylamine hydrochloride, 2-methylallylamine hydrochloride, 4-aminostyrene, vinylamine, and ethynylamine, and is a modified siloxane diamine compound having an amino group at a terminal, and is represented by the following structure:
(In the above chemical formula, G is represented by an organic group having 1 to 50 carbon atoms in the main chain and containing one or more of H atoms, O atoms, N atoms, halogen atoms, and S atoms, X is an organic group having an amino group in the structure, R is a methyl group or a phenyl group , n is an integer of 1 to 50, and m is an integer of 1 to 50.) 2. The modified siloxane diamine compound according to claim 1 , wherein component (C) is allylamine or allylamine hydrochloride. 3. The modified siloxane diamine compound according to claim 1 , wherein the component (A) is a compound represented by the following general formula (a):
(wherein R represents a hydrogen atom or a monovalent organic group having 1 to 50 carbon atoms). A polyimide resin which is a reaction product of the modified siloxane diamine compound according to any one of claims 1 to 3 with a diacid anhydride.