JP6111708B2 - Curable resin composition and electronic component device - Google Patents

Description

  The present invention relates to a curable resin composition and an electronic component device.

  Conventionally, epoxy resins have been widely used in the fields of molding materials, laminates and adhesives. Since these epoxy resins are required to have fast curability from the viewpoint of productivity improvement, a compound that accelerates the curing reaction of the epoxy resin, that is, a curing accelerator is generally used in combination. Also, compositions based on epoxy resins are widely used in the field of sealing technology relating to elements of electronic components such as transistors and ICs. The reason for this is that epoxy resins are balanced in various properties such as moldability, electrical properties, moisture resistance, heat resistance, mechanical properties, and adhesion to inserts.

  In recent years, attention has been focused on power semiconductors such as inverters from the viewpoint of energy saving. Since power semiconductors generate a large amount of heat and may be used in a high temperature environment, there are many opportunities to be exposed to high temperatures. However, a curable resin composition containing an epoxy resin has a problem that heat resistance after curing is low, and development of a curable resin composition having high heat resistance after curing is desired.

  In order to improve the heat resistance after curing of the curable resin composition, a method containing an epoxy resin, a phenol resin, a curing accelerator and a maleimide compound (for example, see Patent Document 1), specified in the same combination as Patent Document 1 A method of using a curing accelerator (see, for example, Patent Document 2) has been proposed.

Japanese Patent Laid-Open No. 01-188518 Japanese Patent Laid-Open No. 03-197527

  However, the method of Patent Document 1 has a problem that the fast curability is low and the moldability is not satisfied. Further, the method of Patent Document 2 has a problem that benzene is released into the environment due to the tetraphenylborate anion during molding and post-curing. An object of the present invention is to provide a curable resin composition excellent in both heat resistance and moldability after curing, and to provide an electronic component device excellent in heat resistance.

  As a result of intensive studies to solve the above problems, the present inventors have obtained a curable resin composition having excellent heat resistance after curing and excellent moldability by using a curing accelerator having a specific structure. As a result, the present invention was completed.

The present invention relates to the following <1> to <7>.
<1> (A) an epoxy resin, (B) a phenol resin, (C) a curing accelerator, and (D) a maleimide compound, wherein (C) the curing accelerator is represented by the following general formula (I-1) A curable resin composition comprising a compound represented by:

In formula (I-1), R ^{1 to} R ³ are each independently a hydrocarbon group having 1 to 18 carbon atoms, and at least one of R ^{1 to} R ³ is an aliphatic group having 1 to 18 carbon atoms. It is a hydrocarbon group, and two or more of R ^{1 to} R ³ may be bonded to each other to form a cyclic structure, and R ^{4 to} R ⁷ are each independently a hydrogen atom, a hydroxyl group or a carbon number of 1 to 18 or more of R ^{4 to} R ⁷ may be bonded to each other to form a cyclic structure.

  <2> (D) The curable resin composition according to <1>, wherein the maleimide compound includes a compound having two or more maleimide groups in one molecule.

  <3> The curable resin composition according to <1> or <2>, further comprising (E) an inorganic filler.

  <4> (A) epoxy resin is biphenyl type epoxy resin, stilbene type epoxy resin, diphenylmethane type epoxy resin, sulfur atom containing type epoxy resin, novolac type epoxy resin, dicyclopentadiene type epoxy resin, triphenylmethane type epoxy resin The curable resin composition according to any one of <1> to <3>, comprising one or more epoxy resins selected from the group consisting of epoxidized products of copolymerization type epoxy resins and aralkyl type phenol resins.

  <5> (B) The phenol resin is an aralkyl type phenol resin, a dicyclopentadiene type phenol resin, a triphenylmethane type phenol resin, a copolymer type phenol resin of a benzaldehyde type phenol resin and an aralkyl type phenol resin, or a novolac type phenol resin. Curable resin composition as described in any one of <1>-<4> containing 1 or more types of phenol resin chosen from the group which consists of.

  <6> (D) The maleimide compound is 4,4′-diphenylmethane dimaleimide, N, N′-1,3-phenylene dimaleimide, 4-methyl-1,3-phenylene bismaleimide, polyphenylmethane maleimide, 2 , 2′-bis [4- (4-maleimidophenoxy) phenyl] propane and 1,6-bismaleimide- (2,2,4-trimethyl) hexane, one or more selected from the group <1> to The curable resin composition as described in any one of <5>.

  <7> An electronic component device comprising an element and a cured product of the curable resin composition according to any one of <1> to <6>, which seals the element.

  ADVANTAGE OF THE INVENTION According to this invention, the curable resin composition excellent in both the heat resistance after hardening and a moldability, and the electronic component apparatus excellent in heat resistance are provided.

  In the present specification, a numerical range indicated using “to” indicates a range including the numerical values described before and after “to” as the minimum value and the maximum value, respectively. Further, in the present specification, the content of each component in the composition is the total amount of the plurality of substances present in the composition unless there is a specific notice when there are a plurality of substances corresponding to each component in the composition. Means.

Hereinafter, the present invention will be described in detail.
[Curable resin composition]
The curable resin composition of the present invention contains (A) an epoxy resin, (B) a phenol resin, (C) a curing accelerator, and (D) a maleimide compound. A compound represented by the formula (I-1) is included.

In formula (I-1), R ^{1 to} R ³ are each independently a hydrocarbon group having 1 to 18 carbon atoms, and at least one of R ^{1 to} R ³ is an aliphatic group having 1 to 18 carbon atoms. It is a hydrocarbon group, and two or more of R ^{1 to} R ³ may be bonded to each other to form a cyclic structure, and R ^{4 to} R ⁷ are each independently a hydrogen atom, a hydroxyl group, or a carbon number of 1 Or an organic group of ˜18, and two or more of R ^{4 to} R ⁷ may be bonded to each other to form a cyclic structure.

The curable resin composition of this invention is excellent in the heat resistance after hardening, and excellent in a moldability by including the compound represented by general formula (I-1) as (C) hardening accelerator. Although the reason is not clear, it is considered that curability is improved when at least one of R ^{1 to} R ³ is an aliphatic hydrocarbon group having 1 to 18 carbon atoms.

  The curable resin composition of the present invention may further contain an inorganic filler in addition to the components (A) to (D). Moreover, you may contain additives, such as a coupling agent, an ion exchanger, a mold release agent, a stress relaxation agent, a flame retardant, and a coloring agent, as needed. Hereinafter, main components constituting the curable resin composition according to the present invention will be described.

(A) Epoxy resin The curable resin composition of the present invention includes (A) an epoxy resin. As the epoxy resin, an epoxy resin having two or more epoxy groups in one molecule can be used. Specifically, phenol novolac type epoxy resin, orthocresol novolac type epoxy resin, phenol, cresol, xylenol, resorcin, catechol, bisphenol A, bisphenol F and other phenol compounds and α-naphthol, β-naphthol, A novolak resin obtained by condensing or co-condensing at least one phenolic compound selected from the group consisting of naphthol compounds such as dihydroxynaphthalene and aliphatic aldehyde compounds such as formaldehyde, acetaldehyde, and propionaldehyde under an acidic catalyst Epoxidized novolac type epoxy resin; obtained by condensation or cocondensation of the above phenolic compound and an aromatic aldehyde compound such as benzaldehyde or salicylaldehyde under an acidic catalyst A triphenylmethane type epoxy resin obtained by epoxidizing a triphenylmethane type phenol resin; a copolymer type epoxy obtained by epoxidizing a novolak resin obtained by cocondensation of the above phenol compound and naphthol compound with an aldehyde compound under an acidic catalyst. Resin; Diphenylmethane type epoxy resin that is diglycidyl ether such as bisphenol A and bisphenol F; Biphenyl type epoxy resin that is diglycidyl ether of alkyl-substituted or unsubstituted biphenol; Stilbene type epoxy that is diglycidyl ether of stilbene phenol compound Resin; Sulfur atom-containing epoxy resin that is diglycidyl ether such as bisphenol S; Glycidi of alcohols such as butanediol, polyethylene glycol, and polypropylene glycol Epoxy resin which is ether; Glycidyl ester type epoxy resin of polyvalent carboxylic acid compounds such as phthalic acid, isophthalic acid, tetrahydrophthalic acid; Active hydrogen bonded to nitrogen atom such as aniline, diaminodiphenylmethane, isocyanuric acid is replaced with glycidyl group Glycidylamine type epoxy resin; dicyclopentadiene type epoxy resin obtained by epoxidizing a co-condensation resin of dicyclopentadiene and a phenol compound; vinylcyclohexene diepoxide obtained by epoxidizing an intramolecular olefin bond; 3,4-epoxycyclohexyl Cycloaliphatic epoxy resins such as methyl-3,4-epoxycyclohexanecarboxylate, 2- (3,4-epoxy) cyclohexyl-5,5-spiro (3,4-epoxy) cyclohexane-m-dioxane; Paraxylylene-modified epoxy resin that is a glycidyl ether of a xylylene-modified phenolic resin; Metaxylylene-modified epoxy resin that is a glycidyl ether of a metaxylylene-modified phenol resin; Terpene-modified epoxy resin that is a glycidyl ether of a terpene-modified phenol resin; Dicyclopentadiene-modified epoxy resin that is ether; cyclopentadiene-modified epoxy resin that is glycidyl ether of cyclopentadiene-modified phenol resin; polycyclic aromatic ring-modified epoxy resin that is glycidyl ether of polycyclic aromatic ring-modified phenol resin; naphthalene ring-containing phenol Naphthalene type epoxy resin which is glycidyl ether of resin; halogenated phenol novolac type epoxy resin; Hydroquinone type epoxy resin; Trimethylolpropane type epoxy resin; Linear aliphatic epoxy resin obtained by oxidizing olefin bond with peracid such as peracetic acid; Diphenylmethane type epoxy resin; Aralkyl type such as phenol aralkyl resin and naphthol aralkyl resin And aralkyl-type epoxy resins that are epoxidized products of phenol resins. These may be used alone or in combination of two or more.

  Among the above epoxy resins, biphenyl type epoxy resin, stilbene type epoxy resin, diphenylmethane type epoxy resin, sulfur atom-containing type epoxy resin, novolac type epoxy resin, dicyclopentadiene type from the viewpoint of the balance between reflow crack resistance and fluidity Epoxy resins selected from the group consisting of epoxy resins, triphenylmethane type epoxy resins, copolymerization type epoxy resins and aralkyl type epoxy resins (these are referred to as “specific epoxy resins”) are preferred. These may be used alone or in combination of two or more.

  When the epoxy resin contains a specific epoxy resin, from the viewpoint of exhibiting the performance of the specific epoxy resin, it is preferable that the total amount of the (A) epoxy resin includes the specific epoxy resin in a total amount of 30% by mass or more, and 50% by mass or more. More preferably.

Among specific epoxy resins, biphenyl type epoxy resins, stilbene type epoxy resins, diphenylmethane type epoxy resins or sulfur atom-containing type epoxy resins are more preferable from the viewpoint of fluidity, and dicyclopentadiene type epoxy is preferable from the viewpoint of heat resistance. A resin, a triphenylmethane type epoxy resin or an aralkyl type epoxy resin is preferred.
Specific examples of preferable epoxy resins are shown below.

The biphenyl type epoxy resin is not particularly limited as long as it is an epoxy resin having a biphenyl skeleton, but an epoxy resin represented by the following general formula (II) is preferable. Among the epoxy resins represented by the following general formula (II), the 3, 3 ′, 5, 5 ′ positions of R ^{8 when} the oxygen atom substitution positions are 4 and 4 ′ positions are methyl groups. , YX-4000H other ^{R 8} is a hydrogen atom (Japan epoxy Resins Co., Ltd., trade name), all ^{R 8} are hydrogen atoms 4,4'-bis (2,3-epoxypropoxy) biphenyl, When all R ⁸ are hydrogen atoms, and the positions where oxygen atoms are substituted in R ⁸ are the 4 and 4 ′ positions, the 3, 3 ′, 5, 5 ′ positions are methyl groups, and the other R YL-6121H (Japan Epoxy Resin Co., Ltd., trade name), which is a mixture when ⁸ is a hydrogen atom, is commercially available.

In the formula (II), R ⁸ represents a hydrogen atom, an alkyl group having 1 to 12 carbon atoms, or an aromatic group having 4 to 18 carbon atoms, and all may be the same or different. n is an average value and shows the number of 0-10.

The stilbene type epoxy resin is not particularly limited as long as it is an epoxy resin having a stilbene skeleton, but an epoxy resin represented by the following general formula (III) is preferable. Among the epoxy resins represented by the following general formula (III), the 3,3 ′, 5,5 ′ positions when R ⁹ is substituted with oxygen atoms at positions 4 and 4 ′ are methyl groups. The other R ⁹ is a hydrogen atom and all of R ¹⁰ are hydrogen atoms, and three of the R ⁹ positions 3, 3 ′, 5, 5 ′ are methyl groups, ESLV-210 (Sumitomo Chemical Co., Ltd., trade name), which is a mixture of the case where one is a tert-butyl group, the other R ⁹ is a hydrogen atom, and all of R ¹⁰ are hydrogen atoms, is commercially available It is available as a product.

In formula (III), R ⁹ and R ^{10 each} represent a hydrogen atom or a monovalent organic group having 1 to 18 carbon atoms, and may be all the same or different. n is an average value and shows the number of 0-10.

The diphenylmethane type epoxy resin is not particularly limited as long as it is an epoxy resin having a diphenylmethane skeleton, and an epoxy resin represented by the following general formula (IV) is preferable. Among the epoxy resins represented by the following general formula (IV), all of R ¹¹ are hydrogen atoms, and 3, 3 ′ when the positions where oxygen atoms are substituted in R ¹² are the 4 and 4 ′ positions. YSLV-80XY (Nippon Steel Chemical Co., Ltd., trade name) in which the methyl groups at the 5 and 5 'positions and the other R ¹² is a hydrogen atom are available as commercial products.

In formula (IV), R ¹¹ and R ^{12 each} represent a hydrogen atom or a monovalent organic group having 1 to 18 carbon atoms, and may be all the same or different. n is an average value and shows the number of 0-10.

As a sulfur atom containing type epoxy resin, if it is an epoxy resin containing a sulfur atom, it will not specifically limit, For example, the epoxy resin shown by the following general formula (V) is mentioned. Among the epoxy resins represented by the following general formula (V), the tert-butyl group is the 3,3 ′ position when the positions where the oxygen atom is substituted in R ¹³ are the 4 and 4 ′ positions, , 6′-position is a methyl group, and other R ¹³ is a hydrogen atom, YSLV-120TE (Nippon Steel Chemical Co., Ltd., trade name) is available as a commercial product.

In the formula (V), R ¹³ represents a hydrogen atom or a monovalent organic group having 1 to 18 carbon atoms, and all may be the same or different. n is an average value and shows the number of 0-10.

The novolak type epoxy resin is not particularly limited as long as it is an epoxy resin obtained by epoxidizing a novolak type phenol resin, and a novolak type phenol resin such as phenol novolak, cresol novolak, naphthol novolak, or the like is glycidyl etherified. Epoxy resins epoxidized using a technique are preferred, and for example, epoxy resins represented by the following general formula (VI) are more preferred. Among the epoxy resins represented by the following general formula (VI), all of R ¹⁴ are hydrogen atoms, R ¹⁵ is a methyl group, and i = 1, ESCN-190, ESCN-195 (Sumitomo Chemical Co., Ltd., (Trade name) etc. are commercially available.

In the formula (VI), R ¹⁴ represents a hydrogen atom or a monovalent organic group having 1 to 18 carbon atoms, and all may be the same or different. R ¹⁵ represents a monovalent organic group having 1 to 18 carbon atoms, and all of them may be the same or different. i represents an integer of 0 to 3 independently. n is an average value and shows the number of 0-10.

  The dicyclopentadiene type epoxy resin is not particularly limited as long as it is an epoxy resin obtained by epoxidizing a compound having a dicyclopentadiene skeleton as a raw material, and an epoxy resin represented by the following general formula (VII) is preferable. Among epoxy resins represented by the following general formula (VII), HP-7200 (DIC Corporation, trade name) in which i = 0 is available as a commercial product.

In the formula (VII), R ¹⁶ represents a monovalent organic group having 1 to 18 carbon atoms, and all may be the same or different. i represents an integer of 0 to 3 independently. n is an average value and shows the number of 0-10.

  The triphenylmethane type epoxy resin is not particularly limited as long as it is an epoxy resin made from a compound having a triphenylmethane skeleton, and a novolak type phenol resin of a compound having a triphenylmethane skeleton and a compound having a phenolic hydroxyl group. A triphenylmethane type epoxy resin such as an epoxy resin obtained by glycidyl etherification of a triphenylmethane type phenol resin such as the above is preferable, and an epoxy resin represented by the following general formula (VIII) is more preferable. Among epoxy resins represented by the following general formula (VIII), 1032H60 (Japan Epoxy Resin Co., Ltd., trade name), iPN = 0, k = 0, EPPN-502H (Nippon Kayaku Co., Ltd., trade name), etc. It is available as a commercial product.

In the formula (VIII), R ¹⁷ and R ¹⁸ each represent a monovalent organic group having 1 to ¹⁸ carbon atoms, and may be all the same or different. i represents an integer of 0 to 3 each independently, and k represents an integer of 0 to 4 independently. n is an average value and shows the number of 0-10.

As a copolymerization type epoxy resin obtained by epoxidizing a novolak resin obtained from a naphthol compound and a phenol compound and an aldehyde compound, as long as it is an epoxy resin using a compound having a naphthol skeleton and a compound having a phenol skeleton as a raw material, there is a particular limitation. However, a novolak type phenol resin using a compound having a naphthol skeleton and a compound having a phenol skeleton is preferably glycidyl etherified, and more preferably an epoxy resin represented by the following general formula (IX). Among the epoxy resins represented by the following general formula (IX), NC-7300 (Nippon Kayaku Co., Ltd., trade name) in which R ²¹ is a methyl group, i = 1, j = 0, k = 0, etc. It is available as a commercial product.

In formula (IX), R ^{19 to} R ²¹ represent a monovalent organic group having 1 to 18 carbon atoms, and may be all the same or different. i is each independently an integer of 0 to 3, j is each independently an integer of 0 to 2, and k is each independently an integer of 0 to 4. Each of l and m is an average value and is a number from 0 to 10, and (l + m) is a number from 0 to 10. The terminal of the epoxy resin represented by the formula (IX) is either the following formula (IX-1) or (IX-2), and the formula (IX) is replaced by the formula (IX-1) or (IX-2). When the terminal structure is bonded, n = 1 when not via a methylene group, and n = 0 when via a methylene group.

  As the epoxy resin represented by the general formula (IX), a random copolymer containing 1 structural unit and m structural units randomly, an alternating copolymer containing alternately, a copolymer containing regularly, Examples thereof include a block copolymer contained in a block shape. Any one of these may be used alone, or two or more may be used in combination.

The epoxidized aralkyl type phenol resin includes at least one selected from the group consisting of phenol compounds such as phenol and cresol, and naphthol compounds such as naphthol and dimethylnaphthol, and dimethoxyparaxylene, bis (methoxymethyl) biphenyl, or derivatives thereof. The epoxy resin is not particularly limited as long as it is made of a phenol resin synthesized from the raw material. For example, glycidyl is a phenol resin synthesized from at least one selected from the group consisting of phenol compounds such as phenol and cresol and naphthol compounds such as naphthol and dimethylnaphthol, and dimethoxyparaxylene, bis (methoxymethyl) biphenyl, or derivatives thereof. Etherified ones are preferable, and epoxy resins represented by the following general formulas (X) and (XI) are more preferable. Among the epoxy resins represented by the following general formula (X), i = 0, R- ³⁸ is a hydrogen atom, NC-3000S (Nippon Kayaku Co., Ltd., trade name), i = 0, R- ³⁸ is a hydrogen atom. CER-3000 (Nippon Kayaku Co., Ltd., trade name) in which an epoxy resin and an epoxy resin in which all R ^{8 in} the general formula (II) are hydrogen atoms are mixed at a weight ratio of 80:20 is commercially available. is there. Among epoxy resins represented by the following general formula (XI), ESN-175 (Nippon Steel Chemical Co., Ltd., trade name) in which i = 0, j = 0, and k = 0 is available as a commercial product. It is.

In the formulas (X) and (XI), R ³⁸ represents a hydrogen atom or a monovalent organic group having 1 to 18 carbon atoms, and each may be the same or different. R ³⁷ and R ^{39 to} R ⁴¹ each represent a monovalent organic group having 1 to 18 carbon atoms, and may be all the same or different. i is independently an integer of 0 to 3, j is independently of an integer of 0 to 2, k is independently of an integer of 0 to 4, and l is independently of an integer of 0 to 6. n is an average value and shows the number of 0-10.

Regarding R ^{8 to} R ²¹ and R ^{37 to} R ^{41 in the} general formulas (II) to (XI), “all may be the same or different” means, for example, 8 to 8 in the formula (II) It means that all 88 R ⁸ may be the same or different. It means that all of R ^{9 to} R ²¹ and R ^{37 to} R ⁴¹ may be the same or different with respect to the respective numbers included in the formula. R ^{8 to} R ²¹ and R ^{37 to} R ⁴¹ may be the same as or different from each other. For example, all of R ⁹ and R ¹⁰ may be the same or different.
Moreover, it is preferable that the C1-C18 organic group in general formula (III)-(XI) is an alkyl group or an aryl group.

  N in the general formulas (II) to (XI) is an average value and is preferably in the range of 0 to 10. If it is 10 or less, the melt viscosity of the component (B) does not become too high, the viscosity at the time of melt molding of the curable resin composition decreases, and unfilled defects and bonding wires (gold wires connecting the element and the lead) Occurrence of deformation is suppressed. More preferably, n is set in the range of 0-4.

  As mentioned above, although the specific example of the preferable epoxy resin which can be used for the curable resin composition of this invention was demonstrated along the said general formula (II)-(XI), as a more specific preferable epoxy resin, a reflow crack-proof From the viewpoint of properties, 4,4′-bis (2,3-epoxypropoxy) -3,3 ′, 5,5′-tetramethylbiphenyl can be mentioned. From the viewpoint of moldability and heat resistance, 4'-bis (2,3-epoxypropoxy) -biphenyl.

  The epoxy equivalent of the epoxy resin is not particularly limited. Among these, from the viewpoint of balance of various properties such as moldability, reflow resistance and electrical reliability, it is preferably 100 g / eq to 1000 g / eq, and more preferably 150 g / eq to 500 g / eq.

  The softening point or melting point of the epoxy resin is not particularly limited. Among these, from the viewpoint of moldability and reflow resistance, the softening point or melting point is preferably 40 ° C to 180 ° C, and from the viewpoint of handleability during preparation of the curable resin composition, it is 50 ° C to 130 ° C. It is more preferable.

  The content of the entire epoxy resin in the curable resin composition is preferably 0.5% by mass to 50% by mass from the viewpoint of strength, fluidity, heat resistance, moldability, and the like, and 2% by mass to 30% by mass. It is more preferable that

(B) Phenol resin The curable resin composition of the present invention contains (B) a phenol resin. There is no restriction | limiting in particular as a kind of phenol resin. For example, the phenol resin or polyhydric phenol which has two or more phenolic hydroxyl groups in 1 molecule generally used as a hardening | curing agent is mentioned. Specifically, compounds having two phenolic hydroxyl groups in one molecule such as resorcin, catechol, bisphenol A, bisphenol F, substituted or unsubstituted biphenol; phenol, cresol, xylenol, resorcin, catechol, bisphenol A, At least one phenolic compound selected from the group consisting of phenolic compounds such as bisphenol F, phenylphenol and aminophenol, and naphtholic compounds such as α-naphthol, β-naphthol and dihydroxynaphthalene, and formaldehyde, acetaldehyde, propionaldehyde, benzaldehyde, A novolak-type phenol resin obtained by condensation or co-condensation with an aldehyde compound such as salicylaldehyde in the presence of an acidic catalyst; the phenolic compound and dimethoxy Aralkyl-type phenol resins such as phenol aralkyl resins and naphthol aralkyl resins synthesized from para-xylene, bis (methoxymethyl) biphenyl, etc .; paraxylylene and / or metaxylylene-modified phenol resins; melamine-modified phenol resins; terpene-modified phenol resins; Dicyclopentadiene-type phenolic resin and dicyclopentadiene-type naphthol resin synthesized by copolymerization of a functional compound and dicyclopentadiene; cyclopentadiene-modified phenol resin; polycyclic aromatic ring-modified phenol resin; biphenyl-type phenol resin; Triphenylmethane type phenol obtained by condensation or cocondensation of an aromatic compound and an aromatic aldehyde compound such as benzaldehyde or salicylaldehyde under an acidic catalyst Le resins; and these two or more phenolic resin obtained by co-polymerization. These phenol resins may be used alone or in combination of two or more.

  Among phenol resins, from the viewpoint of reflow crack resistance, aralkyl type phenol resins, dicyclopentadiene type phenol resins, triphenylmethane type phenol resins, copolymerized phenol resins of benzaldehyde type phenol resins and aralkyl type phenol resins, and A novolac type phenol resin is preferred. These phenolic resins may be used alone or in combination of two or more, but in order to exert their performance, the total amount of phenolic resin is 30% by mass. It is preferable to use more than this, and it is more preferable to use 50 mass% or more.

  The aralkyl type phenol resin is particularly limited as long as it is a phenol resin synthesized from at least one selected from the group consisting of a phenol compound and a naphthol compound and dimethoxyparaxylene, bis (methoxymethyl) biphenyl, or a derivative thereof. However, phenol resins represented by the following general formulas (XII) to (XIV) are preferable.

In the formulas (XII) to (XIV), R ²³ represents a hydrogen atom or a monovalent organic group having 1 to 18 carbon atoms, and all may be the same or different. R ²² , R ²⁴ , R ²⁵ and R ²⁸ each represent a monovalent organic group having 1 to 18 carbon atoms, and each may be the same or different. R ²⁶ and R ^{27 each} represent a hydroxyl group or a monovalent organic group having 1 to 18 carbon atoms, and each may be the same or different. i is each independently an integer of 0 to 3, j is each independently an integer of 0 to 2, k is independently of an integer of 0 to 4, and p is independently of an integer of 0 to 4. n is an average value and shows the number of 0-10.

Among the phenol resins represented by the general formula (XII), MEH-7851 (Maywa Kasei Co., Ltd., trade name) in which i = 0 and R ²³ are all hydrogen atoms is available as a commercial product.

  Among the phenol resins represented by the general formula (XIII), XL-225, XLC (Mitsui Chemicals, Inc., trade name), MEH-7800 (Maywa Kasei Co., Ltd., trade name) where i = 0 and k = 0. Etc. are available as commercial products.

Among the phenolic resins represented by the general formula (XIV), SN-170 (Nippon Steel Chemical Co., Ltd., trade name) where j = 0, k = 0, p = 0, j = 0, k = 1 R ²⁷ is a hydroxyl group, a p = 0 SN-395 (Nippon Steel Chemical Co., Ltd., trade name) and the like are available as commercial products.

  The dicyclopentadiene type phenol resin is not particularly limited as long as it is a phenol resin using a compound having a dicyclopentadiene skeleton as a raw material, and a phenol resin represented by the following general formula (XV) is preferable. Among the phenol resins represented by the following general formula (XV), DPP (Shin Nippon Petrochemical Co., Ltd., trade name) where i = 0 is available as a commercial product.

In the formula (XV), R ²⁹ represents a monovalent organic group having 1 to 18 carbon atoms, and all of them may be the same or different. i represents an integer of 0 to 3 independently. n is an average value and shows the number of 0-10.

  The triphenylmethane type phenol resin is not particularly limited as long as it is a phenol resin using a compound having a triphenylmethane skeleton as a raw material, and a phenol resin represented by the following general formula (XVI) is preferable.

  Among the phenol resins represented by the following general formula (XVI), MEH-7500 (Maywa Kasei Co., Ltd., trade name) in which i = 0 and k = 0 is available as a commercial product.

In formula (XVI), R ³⁰ and R ³¹ each represent a monovalent organic group having 1 to 18 carbon atoms, and may be all the same or different. i represents an integer of 0 to 3 each independently, and k represents an integer of 0 to 4 independently. n is an average value and shows the number of 0-10.

  The copolymer type phenol resin of benzaldehyde type phenol resin and aralkyl type phenol resin is particularly limited as long as it is a copolymer type phenol resin of a phenol resin and an aralkyl type phenol resin using a compound having a benzaldehyde skeleton as a raw material. A phenol resin represented by the following general formula (XVII) is preferable.

  Among the phenolic resins represented by the following general formula (XVII), HE-510 (Air Water Chemical Co., Ltd., trade name) where i = 0, k = 0, q = 0 is available as a commercial product. is there.

In the formula (XVII), R ^{32 to} R ³⁴ represent a monovalent organic group having 1 to 18 carbon atoms, and may be all the same or different. i is each independently an integer of 0 to 3, k is each independently an integer of 0 to 4, and q is each independently an integer of 0 to 5. Each of l and m is an average value of 0 to 11, and (l + m) represents a number of 1 to 11.

  The novolak-type phenol resin is not particularly limited as long as it is a phenol resin obtained by condensing or co-condensing at least one phenolic compound selected from the group consisting of a phenol compound and a naphthol compound and an aldehyde compound under an acidic catalyst. It is not something. Among these, a phenol resin represented by the following general formula (XVIII) is preferable.

Among the phenol resins represented by the following general formula (XVIII) may, i = ^{0, R 35} are all hydrogen atoms TAMANOL 758, 759 (Arakawa Chemical Industries, Ltd., trade name), HP-850N (Hitachi Chemical Co., (Trade name) etc. are commercially available.

In the formula (XVIII), R ³⁵ represents a hydrogen atom or a monovalent organic group having 1 to 18 carbon atoms, and all may be the same or different. R ³⁶ represents a monovalent organic group having 1 to 18 carbon atoms, and all may be the same or different. i represents an integer of 0 to 3 independently. n is an average value and shows the number of 0-10.

“All may be the same or different” described for R ^{22 to} R ³⁶ in the above general formulas (XII) to (XVIII) is, for example, that all i R ^{22s in} formula (XII) are the same. But it means they can be different from each other. For the other R ^{23 to} R ³⁶ , it means that all the numbers contained in the formula may be the same or different from each other. R ^{22 to} R ³⁶ may be the same as or different from each other. For example, all of R ²² and R ²³ may be the same or different, and all of R ³⁰ and R ³¹ may be the same or different.

  N in the general formulas (XII) to (XVIII) is preferably in the range of 0 to 10. If it is 10 or less, the melt viscosity of the resin component does not become too high, the viscosity at the time of melt molding of the curable resin composition also decreases, and unfilled defects and bonding wire (gold wire connecting the element and the lead) are deformed. It becomes difficult to occur. The average n per molecule is preferably set in the range of 0-4.

  In the curable resin composition of the present invention, the blending ratio of (A) the epoxy resin and (B) the phenol resin is the ratio of the total hydroxyl equivalent of all phenol resins to the total epoxy equivalent of the epoxy resin (total hydroxyl groups in the phenol resin). Number / total number of epoxy groups in epoxy resin) is preferably set in the range of 0.10 to 2.0, more preferably in the range of 0.20 to 1.5, and 0.25 to 1. More preferably, it is set to a range of 3. When the ratio is 0.10 or more, the epoxy resin is sufficiently cured and the heat resistance, moisture resistance, and electrical properties of the cured product tend to be further improved. On the other hand, when the ratio is 2.0 or less, the phenol resin component is not excessive, and the curing efficiency is further improved. Furthermore, since a large amount of phenolic hydroxyl group remains in the cured resin, the electrical characteristics and moisture resistance of the package tend to be further improved.

(C) Curing accelerator The curable resin composition of the present invention contains (C) a curing accelerator, and the curing accelerator includes a compound represented by the following general formula (I-1).

In formula (I-1), R ^{1 to} R ³ are each independently a hydrocarbon group having 1 to 18 carbon atoms, and at least one of R ^{1 to} R ³ is an aliphatic group having 1 to 18 carbon atoms. It is a hydrocarbon group, and two or more of R ^{1 to} R ³ may be bonded to each other to form a cyclic structure, and R ^{4 to} R ⁷ are each independently a hydrogen atom, a hydroxyl group or a carbon number of 1 to 18 or more of R ^{4 to} R ⁷ may be bonded to each other to form a cyclic structure.

The “C1-C18 hydrocarbon group” described as R ^{1 to} R ^{3 in the} general formula (I-1) is an aliphatic hydrocarbon group having 1 to 18 carbon atoms and 6 to 18 carbon atoms. Contains some aromatic hydrocarbon groups. From the viewpoint of curability, two or more of R ^{1 to} R ³ in formula (I-1) are preferably an aliphatic hydrocarbon group having 1 to 18 carbon atoms, and all three are 1 to 1 carbon atoms. More preferably, it is 18 aliphatic hydrocarbon groups.

  From the viewpoint of fluidity, the aliphatic hydrocarbon group having 1 to 18 carbon atoms preferably has 1 to 8 carbon atoms, more preferably 2 to 6 carbon atoms, and still more preferably 4 to 6 carbon atoms.

  The aliphatic hydrocarbon group having 1 to 18 carbon atoms may be a linear or branched aliphatic hydrocarbon group having 1 to 18 carbon atoms or an alicyclic hydrocarbon group having 3 to 18 carbon atoms. Also good. From the viewpoint of ease of production, it is preferably a linear or branched aliphatic hydrocarbon group.

  Specific examples of the linear or branched aliphatic hydrocarbon group having 1 to 18 carbon atoms include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, Examples thereof include alkyl groups such as pentyl group, hexyl group, octyl group, decyl group and dodecyl group, allyl group and vinyl group. The linear or branched aliphatic hydrocarbon group may or may not have a substituent. Examples of the substituent include an alkoxy group such as a methoxy group, an ethoxy group, a butoxy group, and a tert-butoxy group, an aryl group such as a phenyl group and a naphthyl group, a hydroxyl group, an amino group, and a halogen atom. The linear or branched aliphatic hydrocarbon group may have two or more substituents, and the substituents in that case may be the same or different. When the linear or branched aliphatic hydrocarbon group has a substituent, the total number of carbon atoms contained in the aliphatic hydrocarbon group and the substituent is preferably 1 to 18. From the viewpoint of curability, an unsubstituted alkyl group is preferable, an unsubstituted alkyl group having 1 to 8 carbon atoms is more preferable, and an n-butyl group, an iso-butyl group, an n-pentyl group, an n-hexyl group, and n An octyl group is more preferred.

  Specific examples of the alicyclic hydrocarbon having 3 to 18 carbon atoms include cycloalkyl groups such as a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclopentenyl group, and a cyclohexenyl group. The alicyclic hydrocarbon group may or may not have a substituent. Substituents include alkyl groups such as methyl, ethyl, butyl, and tert-butyl groups, alkoxy groups such as methoxy, ethoxy, butoxy, and tert-butoxy groups, and aryl groups such as phenyl and naphthyl groups. , Hydroxyl group, amino group, halogen atom and the like. The alicyclic hydrocarbon group may have two or more substituents, and the substituents in that case may be the same or different. When the alicyclic hydrocarbon group has a substituent, the total number of carbon atoms contained in the alicyclic hydrocarbon group and the substituent is preferably 3-18. From the viewpoint of curability, an unsubstituted cycloalkyl group is preferable, an unsubstituted cycloalkyl group having 4 to 10 carbon atoms is more preferable, and a cyclohexyl group, a cyclopentyl group, and a cycloheptyl group are further preferable.

  The aromatic hydrocarbon group having 6 to 18 carbon atoms preferably has 6 to 14 carbon atoms, and more preferably 6 to 10 carbon atoms. The aromatic hydrocarbon group may or may not have a substituent. Substituents include alkyl groups such as methyl, ethyl, butyl, and tert-butyl groups, alkoxy groups such as methoxy, ethoxy, butoxy, and tert-butoxy groups, and aryl groups such as phenyl and naphthyl groups. , Hydroxyl group, amino group, halogen atom and the like. The aromatic hydrocarbon group may have two or more substituents, and the substituents in that case may be the same or different. When the aromatic hydrocarbon group has a substituent, the total number of carbon atoms contained in the aromatic hydrocarbon group and the substituent is preferably 6-18.

  Specific examples of the aromatic hydrocarbon group having 6 to 18 carbon atoms include phenyl group, 1-naphthyl group, 2-naphthyl group, tolyl group, dimethylphenyl group, ethylphenyl group, butylphenyl group, and tert-butyl. Examples thereof include a phenyl group, a methoxyphenyl group, an ethoxyphenyl group, a butoxyphenyl group, and a tert-butoxyphenyl group. The position of the substituent in these aromatic hydrocarbon groups may be any of the ortho, meta, and para positions. From the viewpoint of fluidity, an unsubstituted aryl group having 6 to 12 carbon atoms or 6 to 12 carbon atoms including a substituent is preferable, and an unsubstituted carbon atom having 6 to 10 carbon atoms or a substituent is included. An aryl group of several 6 to 10 is more preferable, and a phenyl group, a p-tolyl group, and a p-methoxyphenyl group are more preferable.

The term “two or more of R ^{1 to} R ³ may be bonded to each other to form a cyclic structure” described as R ^{1 to} R ^{3 in the} general formula (I-1) means that R ^{1 to} R ³ It means that two or three of them are combined to form one divalent or trivalent hydrocarbon group as a whole. Examples of R ^{1 to} R ^{3 in} this case include alkylene groups such as ethylene, propylene, butylene, pentylene, and hexylene that can be bonded to a phosphorus atom to form a cyclic structure, alkenylene groups such as ethylenylene, propylene, and butyleneylene, Substituents that can be bonded to a phosphorus atom to form a cyclic structure, such as an aralkylene group such as a methylenephenylene group, and an arylene group such as phenylene, naphthylene, and anthracenylene. These substituents may be further substituted with an alkyl group, an alkoxy group, an aryl group, an aryloxy group, an amino group, a hydroxyl group, a halogen atom, or the like.

The “organic group having 1 to 18 carbon atoms” described as R ^{4 to} R ^{7 in the} general formula (I-1) has 1 to 18 carbon atoms and may be substituted or unsubstituted. An aromatic hydrocarbon group, an aromatic hydrocarbon group, an aliphatic hydrocarbon oxy group, an aromatic hydrocarbon oxy group, a carbonyl group, an oxycarbonyl group, and a carbonyloxy group.

As an example of the said aliphatic hydrocarbon group and aromatic hydrocarbon, what was mentioned above as an example of the aliphatic hydrocarbon group and aromatic hydrocarbon group represented by R < ¹ > -R < ³ > is mentioned.

  As the aliphatic hydrocarbon oxy group, methoxy group, ethoxy group, propoxy group, isopropoxy group, n-butoxy group, 2-butoxy group, tert-butoxy group, cyclopropyloxy group, cyclohexyloxy group, cyclopentyloxy group An oxy group having a structure in which an oxygen atom is bonded to the above-described aliphatic hydrocarbon group such as an allyloxy group or a vinyloxy group, and these aliphatic hydrocarbon oxy groups are further substituted with an alkyl group, an alkoxy group, an aryl group, an aryloxy group, an amino group. And those substituted with a group, a halogen atom or the like.

  Examples of the aromatic hydrocarbon oxy group include an oxy having a structure in which an oxygen atom is bonded to the above aromatic hydrocarbon group such as a phenoxy group, a methylphenoxy group, an ethylphenoxy group, a methoxyphenoxy group, a butoxyphenoxy group, and a phenoxyphenoxy group. Group, and these aromatic hydrocarbon oxy groups further substituted with an alkyl group, alkoxy group, aryl group, aryloxy group, amino group, halogen atom and the like.

  Examples of the carbonyl group include a formyl group, an acetyl group, an ethylcarbonyl group, a butyryl group, a cyclohexylcarbonyl group, an aliphatic hydrocarbon carbonyl group such as allylcarbonyl, an aromatic hydrocarbon carbonyl group such as a phenylcarbonyl group, and a methylphenylcarbonyl group. These aliphatic hydrocarbon carbonyl groups or aromatic hydrocarbon carbonyl groups are further substituted with an alkyl group, alkoxy group, aryl group, aryloxy group, amino group, halogen atom, and the like.

  Examples of the oxycarbonyl group include aliphatic hydrocarbon oxycarbonyl groups such as methoxycarbonyl group, ethoxycarbonyl group, butoxycarbonyl group, allyloxycarbonyl group, cyclohexyloxycarbonyl group, and aromatic groups such as phenoxycarbonyl group and methylphenoxycarbonyl group. A hydrocarbon oxycarbonyl group or the like, in which these aliphatic hydrocarbon carbonyloxy groups or aromatic hydrocarbon carbonyloxy groups are further substituted with alkyl groups, alkoxy groups, aryl groups, aryloxy groups, amino groups, halogen atoms, etc. Etc.

  Examples of the carbonyloxy group include methylcarbonyloxy group, ethylcarbonyloxy group, butylcarbonyloxy group, allylcarbonyloxy group, cyclohexylcarbonyloxy group and other aliphatic hydrocarbon carbonyloxy groups, phenylcarbonyloxy group, methylphenylcarbonyloxy An aromatic hydrocarbon carbonyloxy group such as a group, and these aliphatic hydrocarbon carbonyloxy groups or aromatic hydrocarbon carbonyloxy groups are further alkyl groups, alkoxy groups, aryl groups, aryloxy groups, amino groups, halogen atoms, etc. And the like substituted with.

The term “two or more R ^{4 to} R ⁷ may be bonded to each other to form a cyclic structure” described as R ^{4 to} R ^{7 in the} general formula (I-1) means two to four Rs. It means that ^{4 to} R ⁷ may be bonded to form one divalent to tetravalent organic group as a whole. R ^{4 to} R ^{7 in} this case include alkylene groups such as ethylene, propylene, butylene, pentylene and hexylene, alkenyl groups such as ethylenylene, propyleneylene and butylene, aralkylene groups such as methylenephenylene, and arylenes such as phenylene, naphthylene and anthracenylene. Substituents that can form a cyclic structure such as a group, and these oxy groups or dioxy groups. These substituents may be further substituted with an alkyl group, an alkoxy group, an aryl group, an aryloxy group, an amino group, a hydroxyl group, a halogen atom, or the like.

R ^{4 to} R ^{7 in the} general formula (I-1) are not particularly limited, and are each independently a hydrogen atom; an alkyl group, an aryl group, an alkoxy group, an aryloxy group that may be substituted. A group; Among these, from the viewpoint of availability of raw materials, an aryl group substituted with at least one selected from the group consisting of a hydrogen atom, an unsubstituted or alkyl group and an alkoxy group, or a chain or cyclic alkyl group is preferable. Examples of the aryl group that is unsubstituted or substituted with at least one selected from the group consisting of an alkyl group and an alkoxy group include a phenyl group, a p-tolyl group, an m-tolyl group, an o-tolyl group, and a p-methoxyphenyl group. Is mentioned. Examples of the chain or cyclic alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a 2-butyl group, a tert-butyl group, an octyl group, and a cyclohexyl group. From the viewpoint of curability, it is preferable that R ^{4 to} R ⁷ are all hydrogen atoms, or that at least one of R ^{4 to} R ⁷ is a hydroxyl group and the rest are all hydrogen atoms.

More preferably, in General Formula (I-1), two or more of R ^{1 to} R ³ are an alkyl group having 1 to 18 carbon atoms or a cycloalkyl group having 3 to 18 carbon atoms, and all of R ^{4 to} R ⁷ are It is a hydrogen atom, or at least one is a hydroxyl group and the rest are all hydrogen atoms. More preferably, R ^{1 to} R ³ are all alkyl groups having 1 to 18 carbon atoms or cycloalkyl groups having ^{3 to} 18 carbon atoms, and R ^{4 to} R ⁷ are all hydrogen atoms, or at least one is a hydroxyl group. And the rest are all hydrogen atoms.

  From the viewpoint of fast curability, the compound represented by the general formula (I-1) is preferably a compound represented by the following general formula (I-2).

In formula (I-2), R ^{1 to} R ³ are each independently a hydrocarbon group having 1 to 18 carbon atoms, and at least one of R ^{1 to} R ³ is an aliphatic group having 1 to 18 carbon atoms. It is a hydrocarbon group, and two or more of R ^{1 to} R ³ may be bonded to each other to form a cyclic structure, and R ^{4 to} R ⁶ are each independently a hydrogen atom or a group having 1 to 18 carbon atoms. It is an organic group, and two or more of R ^{4 to} R ⁶ may be bonded to each other to form a cyclic structure.

Specific examples of ^R 1 to R ⁶ in the formula (I-2) is the same as specific examples of ^R 1 to R ^6, respectively, in formula (I-1), and preferred ranges are also the same. More preferably, two or more of R ^{1 to} R ³ are an alkyl group having 1 to 18 carbon atoms or a cycloalkyl group having ³ to 18 carbon atoms, and R ^{4 to} R ⁶ are all hydrogen atoms. More preferably, all of R ^{1 to} R ³ are an alkyl group having 1 to 18 carbon atoms or a cycloalkyl group having ^{3 to} 18 carbon atoms, and R ^{4 to} R ⁶ are all hydrogen atoms.

  Specific examples of the compound represented by the general formula (I-2) include addition reaction product of tri-n-butylphosphine and 1,4-benzoquinone, addition reaction product of tricyclohexylphosphine and 1,4-benzoquinone, dicyclohexylphenyl. Addition reaction product of phosphine and 1,4-benzoquinone, addition reaction product of cyclohexyl diphenylphosphine and 1,4-benzoquinone, addition reaction product of tri-iso-butylphosphine and 1,4-benzoquinone, tricyclopentylphosphine and 1,4 -Addition reaction product of benzoquinone and the like.

The compound represented by the general formula (I-1) can be synthesized by a known addition reaction. Specifically, both in a solvent in which the corresponding tertiary phosphine such as tri-n-butylphosphine and tricyclohexylphosphine and the corresponding quinone derivative such as 1,4-benzoquinone and 2,5-toluquinone are dissolved together. And a corresponding tertiary phosphine such as tri-n-butylphosphine and tricyclohexylphosphine, and 4-bromophenol, 4-chlorophenol, 3-chlorophenol, 2-chlorophenol, etc. An example is a method in which a halogenated phenol compound is reacted and then subjected to a dehydrohalogenation step. Examples of the solvent include aromatic hydrocarbon solvents, aliphatic hydrocarbon solvents, ketone solvents, alcohol solvents, ether solvents, amide solvents, ester solvents, water, and the like. These solvents may be used alone or in combination of two or more.
The reaction temperature in the addition reaction is not limited as long as the reaction proceeds and the compound (product) represented by the general formula (I-1) to be generated is stably maintained. And from the viewpoint of the stability of the product, it is preferably −20 ° C. to 200 ° C.

  The curable resin composition of this invention may contain 1 or more types of compounds other than the compound shown by general formula (I-1) as another hardening accelerator. Other curing accelerators include 1,5-diazabicyclo [4.3.0] nonene-5 (DBN) and 1,8-diazabicyclo [5.4.0] undecene-7 (DBU). Cyclic amidine compounds such as alkenes, 2-methylimidazole, 2-phenylimidazole, 2-phenyl-4-methylimidazole and 2-heptadecylimidazole; derivatives of the cyclic amidine compounds; phenol novolac salts of the cyclic amidine compounds or derivatives thereof These compounds include maleic anhydride, 1,4-benzoquinone, 2,5-toluquinone, 1,4-naphthoquinone, 2,3-dimethylbenzoquinone, 2,6-dimethylbenzoquinone, 2,3-dimethoxy-5-methyl -1,4-benzoquinone, 2,3-dimethoxy-1,4-benzoquinone, pheny Quinone compounds such as -1,4-benzoquinone, compounds having intramolecular polarization formed by adding a compound having a π bond such as diazophenylmethane; DBU tetraphenylborate salt, DBN tetraphenylborate salt, 2- Cyclic amidinium compounds such as tetraphenylborate salt of ethyl-4-methylimidazole and tetraphenylborate salt of N-methylmorpholine; pyridine, triethylamine, triethylenediamine, benzyldimethylamine, triethanolamine, dimethylaminoethanol, tris (dimethylamino) Tertiary amine compounds such as methyl) phenol; derivatives of the tertiary amine compounds; tetra-n-butylammonium acetate, tetra-n-butylammonium phosphate, tetraethylammonium acetate, tetra-n benzoate -Ammonium salt compounds such as hexylammonium and tetrapropylammonium hydroxide; triphenylphosphine, diphenyl (p-tolyl) phosphine, tris (alkylphenyl) phosphine, tris (alkoxyphenyl) phosphine, tris (alkylalkoxyphenyl) phosphine, Tris (dialkylphenyl) phosphine, Tris (trialkylphenyl) phosphine, Tris (tetraalkylphenyl) phosphine, Tris (dialkoxyphenyl) phosphine, Tris (trialkoxyphenyl) phosphine, Tris (tetraalkoxyphenyl) phosphine, Trialkylphosphine Tertiary phosphine such as dialkylaryl phosphine and alkyldiaryl phosphine; the tertiary phosphine and organic borons Phosphine compounds such as isomers; the tertiary phosphine or the phosphine compound and maleic anhydride, 1,4-benzoquinone, 2,5-toluquinone, 1,4-naphthoquinone, 2,3-dimethylbenzoquinone, 2,6-dimethylbenzoquinone Π bonds such as quinone compounds such as 2,3-dimethoxy-5-methyl-1,4-benzoquinone, 2,3-dimethoxy-1,4-benzoquinone and phenyl-1,4-benzoquinone, diazophenylmethane, etc. A compound having an intramolecular polarization formed by adding a compound having a compound (excluding the compound represented by formula (I-1)); the tertiary phosphine or the phosphine compound and 4-bromophenol, 3-bromophenol, 2- Bromophenol, 4-chlorophenol, 3-chlorophenol, 2-chlorophenol, 4-iodination Phenol, 3-iodophenol, 2-iodophenol, 4-bromo-2-methylphenol, 4-bromo-3-methylphenol, 4-bromo-2,6-dimethylphenol, 4-bromo-3,5 -Dimethylphenol, 4-bromo-2,6-di-tert-butylphenol, 4-chloro-1-naphthol, 1-bromo-2-naphthol, 6-bromo-2-naphthol, 4-bromo-4'-hydroxy A compound having intramolecular polarization obtained by reacting a halogenated phenol compound such as biphenyl and then dehydrohalogenating; a phenyl group bonded to a boron atom such as tetraphenylphosphonium or tetra p-tolylborate Tetrasubstituted phosphonium and tetrasubstituted borates; tetraphenylphosphonium and phenol And salts with compounds and the like.

  Among them, from the viewpoint of reliability, after reacting tertiary phosphine, a compound having intramolecular polarization formed by adding a compound having tertiary bond to phosphine or an intermolecular salt thereof, tertiary phosphine and a halogenated phenol compound. At least one selected from the group consisting of a compound having intramolecular polarization or an intermolecular salt thereof, a tetra-substituted phosphonium, a tetra-substituted borate, and a salt of tetraphenylphosphonium and a phenol compound obtained through a dehydrohalogenation step Preferably, a compound having intramolecular polarization formed by adding a tertiary phosphine compound and a compound having a π bond, or an intermolecular salt thereof, and a dehydrohalogenated compound after reacting the tertiary phosphine compound and the halogenated phenol compound. A group of compounds having intramolecular polarization or their intermolecular salts obtained through the process At least one selected from the above is more preferable.

  As the curing accelerator that can be used in combination with the compound represented by the general formula (I-1), a compound represented by the following general formula (I-3) is more preferable, and the general formula (I-4) or the general formula (I- Even more preferred is the compound represented by 5).

In formula (I-3), R ^{11 to} R ¹³ are each independently an aromatic hydrocarbon group having 1 to 18 carbon atoms, and two or more of R ^{1 to} R ³ are bonded to each other to form a cyclic structure. R ^{14 to} R ¹⁷ are each independently a hydrogen atom, a hydroxyl group, or an organic group having 1 to 18 carbon atoms, and two or more of R ^{14 to} R ¹⁷ are bonded to each other to form a ring. A structure may be formed.

In formula (I-4), R ^{11 to} R ¹³ are each independently an aromatic hydrocarbon group having 1 to 18 carbon atoms, and two or more of R ^{11 to} R ¹³ are bonded to each other to form a cyclic structure. R ^{14 to} R ¹⁷ are each independently a hydrogen atom or an organic group having 1 to 18 carbon atoms, and two or more of R ^{14 to} R ¹⁷ are bonded to each other to form a cyclic structure. It may be formed.

In formula (I-5), R ^{11 to} R ¹³ are each independently an aromatic hydrocarbon group having 1 to 18 carbon atoms, and two or more of R ^{11 to} R ¹³ are bonded to each other to form a cyclic structure. R ^{14 to} R ¹⁶ are each independently a hydrogen atom or an organic group having 1 to 18 carbon atoms, and two or more of R ^{14 to} R ¹⁶ are bonded to each other to form a cyclic structure. It may be formed.

Specific examples of R ^{11 to} R ^{17 in} the general formula (I-3) to the general formula (I-5) are the same as the specific examples of R ^{1 to} R ⁷ in the general formula (I-1), respectively. It is the same.

  When the curable resin composition of the present invention contains a curing accelerator other than the compound represented by the general formula (I-1) as the (C) curing accelerator, it is represented by the general formula (I-1) with respect to the total amount of the curing accelerator. The total content of the compounds to be obtained is preferably 30% by mass or more, more preferably 50% by mass or more, and further preferably 70% by mass or more. When the content is 30% by mass or more, the curability of the curable resin composition is good, and the heat resistance after curing tends to be good.

The amount of the (C) curing accelerator in the curable resin composition of the present invention is not particularly limited as long as a curing acceleration effect can be achieved. From the viewpoint of improving the curability and fluidity at the time of moisture absorption of the curable resin composition, the total amount of the (C) curing accelerator is 0.1 to 30 parts by mass with respect to 100 parts by mass of the total (A) epoxy resin. it is preferably parts by weight, and more preferably 1 part by mass to 15 mass parts. It exists in the tendency which hardens | cures favorably in a short time as content of a hardening accelerator is 0.1 mass part or more. When it is 30 parts by mass or less, the curing rate is not too high and a good molded product tends to be obtained.

(D) Maleimide compound The curable resin composition of the present invention comprises (D) a maleimide compound. By including the maleimide compound, the heat resistance of the curable resin composition after curing is improved. A maleimide compound may be used individually by 1 type, or may combine 2 or more types.

  The type of maleimide compound is not particularly limited as long as the effects of the present invention can be obtained. Specifically, a compound having one maleimide group in a molecule such as N-phenylmaleimide, N-ethylmaleimide, N-cyclohexylmaleimide; 4,4′-diphenylmethanedimaleimide (CAS: 13676-54-5), N, N′-1,3-phenylene dimaleimide (CAS: 3006-93-7), 2,2′-bis [4- (4-maleimidophenoxy) phenyl] propane (CAS: 79922-55-7), 3,3′-dimethyl-5,5′-diethyl-4,4′-diphenylmethane bismaleimide (CAS: 105391-33-1), 4-methyl-1,3-phenylenebismaleimide (CAS: 6422-83-) 9), 1,6-bismaleimide- (2,2,4-trimethyl) hexane (CAS: 39979-46-9), Polyph Methane maleimide (CAS: 67784-74-1) and compounds having two or more maleimide groups in the molecule, such as.

  From the viewpoint of curability, a maleimide compound having two or more maleimide groups in one molecule is preferable. Among these, from the viewpoint of obtaining a cured product having a high glass transition temperature, 4,4′-diphenylmethane dimaleimide (CAS: 13676-54-5), N, N′-1,3-phenylene dimaleimide (CAS: 3006). -93-7), 4-methyl-1,3-phenylenebismaleimide (CAS: 6422-83-9) and polyphenylmethanemaleimide (CAS: 67784-74-1) are more preferable, and from the viewpoint of long-term heat resistance. 2,2′-bis [4- (4-maleimidophenoxy) phenyl] propane (CAS: 79922-55-7) is more preferable, and from the viewpoint of fluidity, 1,6-bismaleimide- (2,2 , 4-trimethyl) hexane (CAS: 39979-46-9) is more preferred.

  Content of (D) maleimide compound in the curable resin composition of this invention will not be specifically limited if the effect of this invention is acquired, ((A) component) + ((B) component) )): ((D) component) is preferably contained in a ratio of 1:20 to 20: 1, more preferably in a ratio of 1:10 to 10: 1, and 1: 5 to 5: 1. More preferably, it is contained in a proportion of

(E) Inorganic filler The curable resin composition of the present invention may further contain (E) an inorganic filler as necessary. In particular, when the curable resin composition is used as a molding material for sealing, it is preferable to contain an inorganic filler.

  The inorganic filler is not particularly limited as long as it is generally used for a sealing molding material. For example, fused silica, crystalline silica, glass, alumina, calcium carbonate, zirconium silicate, calcium silicate, silicon nitride, aluminum nitride, boron nitride, beryllia, zirconia, zircon, fosterite, steatite, spinel, mullite, titania, Examples include talc, clay, mica and other fine powders, and beads formed by spheroidizing these. An inorganic filler having a flame retardant effect may be used. Examples of the inorganic filler having a flame retardant effect include aluminum hydroxide, magnesium hydroxide, composite metal hydroxide such as composite hydroxide of magnesium and zinc, zinc borate and the like. Among these, fused silica is preferable from the viewpoint of reducing the linear expansion coefficient, and alumina is preferable from the viewpoint of high thermal conductivity. These inorganic fillers may be used alone or in combination of two or more.

  There is no restriction | limiting in particular in the content rate in case a curable resin composition contains an inorganic filler, It is preferable that it is 55 volume%-90 volume% in the total amount of a curable resin composition from a viewpoint of fluidity | liquidity and intensity | strength, It is more preferably 60% by volume to 90% by volume, and further preferably 60% by volume to 85% by volume. When the content of the inorganic filler in the curable resin composition is 55% by volume or more, characteristics such as the thermal expansion coefficient, thermal conductivity, and elastic modulus of the cured product tend to be further improved. When it is 90% by volume or less, an increase in the viscosity of the curable resin composition is suppressed, and the fluidity is further improved and the moldability tends to be better.

The average particle size of the inorganic filler is preferably 1 μm to 50 μm, more preferably 10 μm to 30 μm. There exists a tendency for the raise of the viscosity of curable resin composition to be suppressed more as an average particle diameter is 1 micrometer or more. When the average particle size is 50μm or less, separation of the epoxy resin component and the inorganic Filling agent is suppressed, the uniformity is improved in the cured product, the variation of the cured product characteristics are more effectively suppressed, narrow gap There exists a tendency for the filling property to improve more. The average particle size of the inorganic filler can be measured as a volume average particle size by a laser scattering diffraction particle size distribution analyzer.

  From the viewpoint of fluidity of the curable resin composition, the particle shape of the inorganic filler is preferably spherical rather than square, and the particle size distribution of the inorganic filler is preferably distributed over a wide range. For example, when the content of the inorganic filler in the curable resin composition is 75% by volume or more, the inorganic filler is distributed in a wide range of 70% by volume or more in a spherical shape and a particle size distribution of 0.1 μm to 80 μm. It is preferable to occupy. Since such inorganic fillers tend to have a close-packed structure, an increase in viscosity is suppressed even when the content in the curable resin composition is increased, and a curable resin composition having superior fluidity is obtained. Can do.

[Various additives]
The curable resin composition of the present invention further contains various additives such as a coupling agent, an ion exchanger, a release agent, a stress relaxation agent, a flame retardant, and a colorant exemplified below in addition to the above components. May be. In addition, the curable resin composition of this invention may contain the various additives well-known in this technical field other than the additive illustrated below as needed.

(Coupling agent)
The curable resin composition of the present invention may contain a coupling agent as necessary in order to enhance the adhesion between the epoxy resin component and the inorganic filler. Examples of the coupling agent include known coupling agents such as silane compounds such as epoxy silane, mercapto silane, amino silane, alkyl silane, ureido silane, and vinyl silane, titanium compounds, aluminum chelate compounds, and aluminum / zirconium compounds. .

  When the curable resin composition contains a coupling agent, the content of the coupling agent in the curable resin composition is preferably 0.05% by mass to 5% by mass with respect to the inorganic filler, More preferably, it is 0.1 mass%-2.5 mass%. There exists a tendency for adhesiveness with a flame | frame to improve that the content rate with respect to an inorganic filler is 0.05 mass% or more. There exists a tendency for the moldability of a package to improve that it is 5 mass% or less.

(Ion exchanger)
The curable resin composition of the present invention may contain an ion exchanger as necessary. In particular, when a curable resin composition is used as a molding material for sealing, it may contain an ion exchanger from the viewpoint of improving the moisture resistance and high temperature storage characteristics of an electronic component device provided with an element to be sealed. preferable. There is no restriction | limiting in particular as an ion exchanger, A conventionally well-known thing can be used. Specific examples include hydrotalcite compounds and hydrous oxides of at least one element selected from the group consisting of magnesium, aluminum, titanium, zirconium and bismuth. These ion exchangers can be used alone or in combination of two or more. Especially, the hydrotalcite shown by the following general formula (A) is preferable.

Mg _(1-X) Al _X (OH) ₂ (CO ₃ ) _{X / 2} · mH ₂ O (A)
(0 <X ≦ 0.5, m is a positive number)

  When the curable resin composition contains an ion exchanger, the content is not particularly limited as long as it is an amount sufficient to trap ions such as halogen ions. For example, it is preferably 0.1% by mass to 30% by mass and more preferably 1% by mass to 5% by mass with respect to the total amount of the epoxy resin.

(Release agent)
The curable resin composition of the present invention may contain a release agent from the viewpoint of obtaining good release properties from the mold during molding. There is no restriction | limiting in particular as a mold release agent, A conventionally well-known thing can be used. Specific examples include carnauba wax, higher fatty acids such as montanic acid and stearic acid, higher fatty acid metal salts, ester waxes such as montanic acid esters, and polyolefin waxes such as oxidized polyethylene and non-oxidized polyethylene. These release agents may be used alone or in combination of two or more. Among these, carnauba wax is preferable. As the polyolefin-based wax, low molecular weight polyethylene having a number average molecular weight of about 500 to 10,000, such as H4, PE, PED series manufactured by Hoechst Co., Ltd., can be mentioned as a commercially available product.

  When the curable resin composition contains a release agent, the content is preferably 0.01% by mass to 10% by mass, and more preferably 0.1% by mass to 5% by mass with respect to the total amount of the epoxy resin. If the content of the release agent is 0.01% by mass or more, the release property tends to be sufficiently obtained. There exists a tendency for more favorable adhesiveness to be acquired as it is 10 mass% or less.

(Stress relaxation agent)
The curable resin composition of the present invention may contain a stress relaxation agent such as silicone oil and silicone rubber powder, if necessary. By containing the stress relaxation agent, warpage deformation of the package and generation of package cracks can be further reduced. As a stress relaxation agent, if it is a well-known flexible agent (stress relaxation agent) generally used, it will not specifically limit. Specifically, silicone-based, styrene-based, olefin-based, urethane-based, polyester-based, polyether-based, polyamide-based, polybutadiene-based thermoplastic elastomers, NR (natural rubber), NBR (acrylonitrile-butadiene rubber), acrylic Rubber particles such as rubber, urethane rubber and silicone powder, core-shell such as methyl methacrylate-styrene-butadiene copolymer (MBS), methyl methacrylate-silicone copolymer, methyl methacrylate-butyl acrylate copolymer Examples thereof include rubber particles having a structure. These flexible agents may be used alone or in combination of two or more. Of these, silicone-based flexible agents are preferred. Examples of the silicone-based flexible agent include those having an epoxy group, those having an amino group, and those obtained by modifying these with a polyether.

(Flame retardants)
The curable resin composition of this invention may contain a flame retardant as needed from a viewpoint of providing a flame retardance. There is no restriction | limiting in particular as a flame retardant, It can select suitably from the well-known flame retardant generally used. Specific examples include known organic or inorganic compounds containing a halogen atom, antimony atom, nitrogen atom or phosphorus atom, metal hydroxides, and the like. These flame retardants may be used alone or in combination of two or more. When the curable resin composition contains a flame retardant, the content is not particularly limited as long as the flame retardant effect is achieved. For example, 1% by mass to 30% by mass is preferable with respect to the total amount of the epoxy resin, and 2% by mass to 15% by mass is more preferable.

(Coloring agent)
The curable resin composition of the present invention may further contain a colorant as necessary. Examples of the colorant include known colorants such as carbon black, organic dyes, organic pigments, titanium oxide, red lead, and bengara. The content of the colorant can be appropriately selected according to the purpose and the like.

  The method for preparing the curable resin composition is not particularly limited, and any method can be used as long as various components can be uniformly dispersed and mixed. As a general technique, there can be mentioned a method in which components of a predetermined blending amount are sufficiently mixed by a mixer or the like, and then melt-kneaded by a mixing roll, an extruder or the like, cooled and pulverized. More specifically, for example, predetermined amounts of the above-mentioned components are uniformly stirred and mixed, kneaded with a kneader, roll, extruder, etc., which has been heated to 70 ° C. to 140 ° C., cooled, and pulverized. Can be obtained at The curable resin composition is easy to handle if it is tableted in a size and weight that meets the molding conditions of the package.

<Electronic component device>
The electronic component device of the present invention includes an element and a cured product of the above-described curable resin composition that seals the element. An electronic component device produced using the curable resin composition of the present invention is excellent in reliability. Electronic component devices include lead frames, pre-wired tape carriers, wiring boards, glass, silicon wafers and other support members, semiconductor chips, transistors, diodes, thyristors and other active elements, capacitors, resistors, coils and other passive components. What sealed the element part obtained by mounting elements, such as an element, with the curable resin composition of this invention is mentioned. More specifically, after fixing the semiconductor element on the lead frame, connecting the terminal part of the element such as a bonding pad and the lead part by wire bonding, bump, etc., then using the curable resin composition of the present invention. DIP (Dual Inline Package), PLCC (Plastic Leaded Chip Carrier), QFP (Quad Flat Package), SOP (Small Outline Package), SOJ (Small Outlet Jck), SOJ (Small Outlet Jck), having a structure sealed by transfer molding or the like. (Thin Small Outline Package), TQFP (Thin Quad Flat Package) and other general resin-encapsulated ICs; connected to the tape carrier by bumps TCP (Tape Carrier Package) having a structure in which a conductor chip is sealed with the curable resin composition of the present invention; a semiconductor connected to a wiring formed on a wiring board or a glass plate by wire bonding, flip chip bonding, solder or the like It has a structure in which at least one element selected from the group consisting of active elements such as chips, transistors, diodes and thyristors and passive elements such as capacitors, resistors and coils is sealed with the curable resin composition of the present invention. COB (Chip On Board) module, hybrid IC, multi-chip module, etc .; the element is mounted on the surface of the organic substrate on which the wiring board connection terminal is formed on the back surface, and is formed on the element and the organic substrate by bump or wire bonding After connecting the wiring, the curable resin composition of the present invention BGA having the structure sealing the child (Ball Grid Array), CSP (Chip Size Package) and the like. Moreover, the curable resin composition of this invention can be used effectively also in a wiring board.

  As a method for sealing an electronic component device using the curable resin composition of the present invention, a low-pressure transfer molding method is common, but an injection molding method, a compression molding method, or the like may be used.

  Hereinafter, the present invention will be described more specifically with reference to examples. However, the scope of the present invention is not limited to the examples shown below.

(Preparation of curable resin composition)
The following were prepared as epoxy resins.
Epoxy resin 1: triphenylmethane type epoxy resin having an epoxy equivalent of 168 and a softening point of 62 ° C. (product name: 1032H60, manufactured by Japan Epoxy Resin Co., Ltd.)
Epoxy resin 2: Orthocresol novolac type epoxy resin having an epoxy equivalent of 195 and a softening point of 60 ° C. (trade name N-500P1 manufactured by DIC Corporation)
Epoxy resin 3: biphenylene aralkyl type epoxy resin having an epoxy equivalent of 282 and a softening point of 56 ° C. (trade name NC-3000, manufactured by Nippon Kayaku Co., Ltd.)

The following were prepared as phenolic resins.
Phenol resin 1: Triphenylmethane type phenol resin having a hydroxyl group equivalent of 103 and a softening point of 84 ° C. (trade name HE-910-10, manufactured by Air Water Co., Ltd.)
Phenol resin 2: 1,6-dihydroxynaphthalene aralkyl resin having a hydroxyl equivalent weight of 110 and a softening point of 95 ° C. (trade name HE-910-10, manufactured by Nippon Steel Chemical Co., Ltd.)
Phenol resin 3: phenol novolak resin having a hydroxyl group equivalent of 106 and a softening point of 85 ° C. (trade name HP-850N, manufactured by Hitachi Chemical Co., Ltd.)
Phenol resin 4: Biphenylene aralkyl type phenol resin having a hydroxyl group equivalent of 190 and a softening point of 80 ° C. (trade name HE-200C-10, manufactured by Air Water Co., Ltd.)

The following was prepared as a curing accelerator having a structure represented by the general formula (I-1).
Curing accelerator 1: addition reaction product of tri-n-butylphosphine and 1,4-benzoquinone Curing accelerator 2: addition reaction product of tricyclohexylphosphine and 1,4-benzoquinone Curing accelerator 3: dicyclohexylphenylphosphine Reaction product of 1,4-benzoquinone and curing accelerator 4: addition reaction product of cyclohexyldiphenylphosphine and 1,4-benzoquinone

The following were prepared as comparative curing accelerators.
Curing accelerator A: Triphenylphosphine Curing accelerator B: Tri-p-tolylphosphine Curing accelerator C: 1,8-diazabicyclo [5.4.0] undec-7-ene Curing accelerator D: Addition reaction product of triphenylphosphine and 1,4-benzoquinone / curing accelerator E: Addition reaction product of tri-p-tolylphosphine and 1,4-benzoquinone

The following were prepared as maleimide compounds.
Maleimide 1: Polyphenylmethane maleimide (manufactured by Daiwa Kasei Kogyo Co., Ltd., trade name BMI-2300)
Maleimide 2: 4,4'-diphenylmethane dimaleimide (manufactured by Daiwa Kasei Kogyo Co., Ltd., trade name BMI-1000)
Maleimide 3: 2,2′-bis [4- (4-maleimidophenoxy) phenyl] propane (manufactured by Daiwa Kasei Kogyo Co., Ltd., trade name BMI-4000)
Maleimide 4: 3,3′-dimethyl-5,5′-diethyl-4,4′-diphenylmethane bismaleimide (manufactured by Daiwa Kasei Kogyo Co., Ltd., trade name BMI-5100) was prepared.

The following were prepared as inorganic fillers.
-Spherical fused silica having an average particle size of 17.5 μm and a specific surface area of 3.8 m ² / g

In addition, the following were prepared as various additives.
Coupling agent: Epoxy silane (γ-glycidoxypropyltrimethoxysilane)
Colorant: Carbon black (trade name MA-100, manufactured by Mitsubishi Chemical Corporation)
・ Release agent: Carnauba wax (manufactured by Celerica NODA)

  By blending the above-mentioned components in parts by mass shown in Table 1 and Table 2 and performing roll kneading under conditions of a kneading temperature of 80 ° C. and a kneading time of 15 minutes, Examples 1 to 15 and Comparative Examples 1 to 8, respectively. A curable resin composition was obtained. In Examples 7 to 9, before carrying out roll kneading to uniformly disperse the maleimide compound, the maleimide compound and the phenol resin as the curing agent were premixed at 120 ° C. for 30 minutes, and then the other components were mixed. Combined with ingredients. A blank in the table indicates that the corresponding component is not included.

[Characteristic evaluation of curable resin composition]
Next, the curable resin compositions obtained in Examples 1 to 15 and Comparative Examples 1 to 8 were evaluated by various tests shown below. The evaluation results are shown in Tables 3 and 4. The curable resin composition was molded using a transfer molding machine under conditions of a mold temperature of 180 ° C., a molding pressure of 6.9 MPa, and a curing time of 90 seconds. Further, post-curing was performed at 250 ° C. for 6 hours.

(1) Spiral flow (fluidity index)
A curable resin composition was molded under the above conditions using a spiral flow measurement mold according to EMMI-1-66. Next, the flow distance (cm) of the molded product of the curable resin composition was measured.

(2) Hardness upon heating The curable resin composition was molded into a disk having a diameter of 50 mm and a thickness of 3 mm under the above conditions. Immediately after molding, the hardness of the molded product of the curable resin composition was measured using a Shore D hardness meter.

(3) Glass transition temperature (TMA)
The curable resin composition was molded into a 3.0 mm × 3.0 mm × 19 mm test piece under the above conditions and post-cured. Subsequently, the linear expansion curve was measured using a thermal analysis system (TMA / SS6000) manufactured by Seiko Instruments Inc. at a temperature rising rate of 5 ° C./min, and the inflection point was defined as the glass transition temperature (TMA) (° C.). .

(4) Glass transition temperature (DMA)
The curable resin composition was molded into a size of 80 mm length × 10 mm width × 3 mm thickness under the above conditions and post-cured. Next, it is cut into a length of 55 mm with a diamond cutter, using a viscoelasticity measuring device ARES (manufactured by Rheometric Scientific FE Co., Ltd.) in a dynamic mode under conditions of a heating rate of 5 ° C. and a frequency of 6.28 rad / s. The glass transition temperature (DMA) (° C.) was determined from the measurement of tan δ.

(5) 250 ° C. elastic modulus / 60 ° C. elastic modulus (index of heat resistance)
The storage elastic modulus at 60 ° C. and 250 ° C. was determined from the measurement in (4) above, and the ratio of the elastic modulus at 250 ° C. to the elastic modulus at 60 ° C. was calculated. It means that the larger the obtained value, the smaller the difference from room temperature at high temperature, and it can be judged that the heat resistance after curing is excellent.

  As can be seen from the results shown in Table 3 and Table 4, each of the curable resin compositions of Examples 1 to 15 has a large value of 250 ° C. elastic modulus / 60 ° C. elastic modulus, which is an index of heat resistance after curing. The glass transition temperature was also high. All of them were excellent in spiral flow and hot hardness and could be molded well.

  On the other hand, Comparative Examples 1 and 2, which do not contain a maleimide compound, had a small value of 250 ° C. elastic modulus / 60 ° C. elastic modulus, which is an index of heat resistance, and had insufficient heat resistance after curing. Further, in Comparative Examples 3 to 7 containing a different kind of curing accelerator from the compound represented by the general formula (I-1), the value of 250 ° C. elastic modulus / 60 ° C. elastic modulus, which is an index of heat resistance, is small. Furthermore, since the spiral flow and the hot hardness are low, there is a possibility that a problem occurs in the formability. Further, in Comparative Example 8 containing no epoxy resin or phenol resin, it was impossible to mold because it was not cured under molding conditions.

Claims (7)

It contains (A) an epoxy resin, (B) a phenol resin, (C) a curing accelerator, and (D) a maleimide compound, and (C) the curing accelerator is represented by the following general formula (I-1). A curable resin composition containing a compound.


(In Formula (I-1), R ^{1 to} R ³ are each independently a hydrocarbon group having 1 to 18 carbon atoms, and at least one of R ^{1 to} R ³ is a fatty acid having 1 to 18 carbon atoms. 2 or more of R ^{1 to} R ³ may be bonded to each other to form a cyclic structure, and R ^{4 to} R ⁷ are each independently a hydrogen atom, a hydroxyl group or a carbon number of 1 -18 organic groups, and two or more of R ^{4 to} R ⁷ may be bonded to each other to form a cyclic structure.)   (D) The curable resin composition of Claim 1 in which a maleimide compound contains the compound which has a 2 or more maleimide group in 1 molecule.   The curable resin composition according to claim 1 or 2, further comprising (E) an inorganic filler.   (A) Epoxy resin is biphenyl type epoxy resin, stilbene type epoxy resin, diphenylmethane type epoxy resin, sulfur atom containing type epoxy resin, novolac type epoxy resin, dicyclopentadiene type epoxy resin, triphenylmethane type epoxy resin, copolymerization The curable resin composition of any one of Claims 1-3 containing 1 or more types of epoxy resins chosen from the group which consists of an epoxy resin of a type epoxy resin and an aralkyl type phenol resin.   (B) A group in which the phenol resin is composed of an aralkyl type phenol resin, a dicyclopentadiene type phenol resin, a triphenylmethane type phenol resin, a copolymer type phenol resin of a benzaldehyde type phenol resin and an aralkyl type phenol resin, and a novolac type phenol resin. The curable resin composition according to any one of claims 1 to 4, further comprising at least one phenol resin selected from the above.   (D) The maleimide compound is 4,4′-diphenylmethane dimaleimide, N, N′-1,3-phenylene dimaleimide, 4-methyl-1,3-phenylene bismaleimide, polyphenylmethane maleimide, 2,2 ′. 6. One or more selected from the group consisting of -bis [4- (4-maleimidophenoxy) phenyl] propane and 1,6-bismaleimide- (2,2,4-trimethyl) hexane. The curable resin composition according to any one of the above.   The electronic component apparatus containing an element and the hardened | cured material of the curable resin composition of any one of Claims 1-6 which has sealed the said element.