JP5177344B2 - Room temperature curable organopolysiloxane composition - Google Patents

Description

  The present invention relates to a room temperature curable organopolysiloxane composition, and more particularly to a room temperature curable organopolysiloxane composition that gives a cured product excellent in storage stability, moisture resistance, and water resistance.

  Conventionally, various types of room temperature curable organopolysiloxane compositions that are cured in an elastomeric form at room temperature by contact with moisture in the air are known, and in particular, those that cure by releasing alcohol. It is characterized by the fact that it has no unpleasant odor and does not corrode metals, and is preferably used for sealing, bonding, and coating of electrical and electronic equipment.

  Representative examples of this type include those described in JP-B-39-27643 (Patent Document 1), which discloses a composition comprising a hydroxyl-terminated organopolysiloxane, an alkoxysilane, and an organic titanium compound. Has been. JP-A-55-43119 (Patent Document 2) discloses a composition comprising an alkoxysilyl end-capped organopolysiloxane, an alkoxysilane, and an alkoxytitanium. Japanese Examined Patent Publication No. 7-39547 (Patent Document 3) discloses a composition comprising an alkoxysilyl end-capped linear organopolysiloxane containing a silethylene group, an alkoxysilane, and an alkoxytitanium. Further, JP-A-7-331076 (Patent Document 4) discloses a composition comprising a hydroxyl group-endcapped organopolysiloxane or an alkoxy group-endcapped organopolysiloxane and an alkoxy-α-silyl ester compound.

  These compositions have some degree of storage stability, water resistance and moisture resistance, but have not yet completely solved these problems.

Japanese Examined Patent Publication No. 39-27643 Japanese Patent Laid-Open No. 55-43119 Japanese Examined Patent Publication No. 7-39547 Japanese Patent Laid-Open No. 7-331076

  The present invention has been made in view of the above circumstances, and an object thereof is to provide a room temperature-curable organopolysiloxane composition that provides a cured product having excellent storage stability and excellent water resistance and moisture resistance.

  As a result of intensive studies to achieve the above object, the present inventor has converted a silyl ketene acetal type compound having a specific molecular structure represented by the following formula (1) into a polymer terminal blocking agent, a curing agent, and storage stability. It has been found that by using it as an agent, a room temperature-curable organopolysiloxane composition that gives a cured product having excellent storage stability, water resistance and moisture resistance can be obtained, and the present invention has been made.

（式中、Ｒ、Ｒ¹及びＲ²は、置換又は非置換の炭素原子数１〜１２の一価炭化水素基であり、同一でも異なっていてもよく、ｎは１〜６の整数、ａは１〜３の整数を示す。）
で表されるシリルケテンアセタール型化合物、その部分加水分解縮合物又はそれらの混合物
を含有してなる室温硬化性オルガノポリシロキサン組成物を提供する。
また、本発明の組成物には、前記（Ａ）、（Ｂ）成分に加えて、（Ｃ）充填剤及び／又は（Ｄ）有機金属触媒を配合することができる。 Therefore, the present invention
(A) a diorganopolysiloxane having a hydroxyl group or hydrolyzable group bonded to at least two silicon atoms in the molecule;
(B) The following general formula (1)

Wherein R, R ¹ and R ² are substituted or unsubstituted monovalent hydrocarbon groups having 1 to 12 carbon atoms, which may be the same or different, and n is an integer of 1 to 6, a Represents an integer of 1 to 3.)
A room temperature-curable organopolysiloxane composition comprising a silyl ketene acetal type compound represented by the above, a partially hydrolyzed condensate thereof, or a mixture thereof is provided.
In addition to the components (A) and (B), the composition of the present invention may contain (C) a filler and / or (D) an organometallic catalyst.

  The organopolysiloxane composition of the present invention gives a cured product particularly excellent in moisture resistance and water resistance. Further, for example, even after storage for 6 months, it rapidly cures when exposed to the air and exhibits excellent physical properties. . This composition is useful for bonding and sealing materials where water resistance and moisture resistance are required, and in particular, it should be used effectively as a building application requiring electrical resistance to steam and water and as an adhesive for electrical and electronic applications. Can do.

Hereinafter, the present invention will be described in more detail.
The room temperature curable organopolysiloxane composition of the present invention comprises:
(A) a diorganopolysiloxane having a hydroxyl group or hydrolyzable group bonded to at least two silicon atoms in the molecule;
(B) A silyl ketene acetal type compound represented by the general formula (1), a partially hydrolyzed condensate thereof or a mixture thereof, preferably (C) a filler,
(D) An organometallic catalyst can be blended.

（式中、Ｒは置換又は非置換の炭素数１〜１２の一価炭化水素基であり、Ｘは酸素原子又は炭素原子数１〜８の二価炭化水素基であり、Ｙは加水分解性基であり、ｂは２又は３であり、ｍはこのジオルガノポリシロキサンの２５℃における粘度を１００〜１，０００，０００ｍＰａ・ｓとする数である。） [(A) component]
The diorganopolysiloxane as the component (A) is the main agent (base polymer) of the room temperature curable organopolysiloxane composition of the present invention, and is a hydroxyl group or hydrolyzable group bonded to at least two silicon atoms in the molecule. It is what has. As such a diorganopolysiloxane, specifically, a diorganopolysiloxane in which a molecular chain terminal represented by the following general formula (2) or (3) is blocked with a hydroxyl group or a hydrolyzable group is used.

(In the formula, R is a substituted or unsubstituted monovalent hydrocarbon group having 1 to 12 carbon atoms, X is an oxygen atom or a divalent hydrocarbon group having 1 to 8 carbon atoms, and Y is hydrolyzable. And b is 2 or 3, and m is a number that makes the viscosity of this diorganopolysiloxane at 25 ° C. 100 to 1,000,000 mPa · s.)

  In the above formula, the substituted or unsubstituted monovalent hydrocarbon group of R includes methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group, octadecyl Alkyl group such as a group; cycloalkyl group such as cyclopentyl group and cyclohexyl group; alkenyl group such as vinyl group, allyl group, butenyl group, pentenyl group, hexenyl group; phenyl group, tolyl group, xylyl group, α-, β- Aryl groups such as naphthyl group; aralkyl groups such as benzyl group, 2-phenylethyl group and 3-phenylpropyl group; and some or all of hydrogen atoms of these groups are halogen atoms such as F, Cl and Br. And a group substituted with cyano group or the like, for example, 3-chloropropyl group, 3,3,3-trifluoropropyl group, 2-cyanoethyl group, etc. be able to. Among these, a methyl group and an ethyl group are preferable, and a methyl group is particularly preferable.

X is an oxygen atom or a divalent hydrocarbon group having 1 to 8 carbon atoms, and the divalent hydrocarbon group is represented by — (CH ₂ ) _p — (p represents 1 to 8). Among these, an oxygen atom and —CH ₂ CH ₂ — are preferable.

  Y is a hydrolyzable group at the molecular chain end of the diorganopolysiloxane, for example, an alkoxy group such as a methoxy group, an ethoxy group or a propoxy group; an alkoxyalkoxy such as a methoxyethoxy group, an ethoxyethoxy group or a methoxypropoxy group Group, acetoxy group, octanoyloxy group, benzoyloxy group and other acyloxy groups, vinyloxy group, isopropenyloxy group, 1-ethyl-2-methylvinyloxy group and other alkenyloxy groups, dimethyl ketoxime group, methyl ethyl ketoxime group Ketoxime groups such as diethyl ketoxime group, amino groups such as dimethylamino group, diethylamino group, butylamino group, cyclohexylamino group, aminoxy groups such as dimethylaminoxy group, diethylaminoxy group, N-methylacetamide group, N- Chill acetamide group, and amide groups such as N- methylbenzamide group. Among these, an alkoxy group is particularly preferable.

  The diorganopolysiloxane of component (A) preferably has a viscosity at 25 ° C. of 100 to 1,000,000 mPa · s, more preferably 300 to 500,000 mPa · s, particularly preferably 500 to 100,000 mPa · s, In particular, it is 1,000 to 80,000 mPa · s. When the viscosity of the diorganopolysiloxane is less than 100 mPa · s, it may be difficult to obtain a coating film having excellent physical and mechanical strength. When the viscosity exceeds 1,000,000 mPa · s, the composition In some cases, the viscosity of the product becomes too high, and the workability during use may deteriorate. Here, the viscosity is a numerical value measured by a rotational viscometer.

（式中、ｍ、Ｒ、Ｙは上記と同様であり、ｂ′は０又は１である。） Specific examples of the (A) component diorganopolysiloxane include the following.

(In the formula, m, R and Y are the same as above, and b ′ is 0 or 1.)

  The diorganopolysiloxane of component (A) can be used singly or in combination of two or more having different structures and molecular weights.

[Component (B)]
The component (B) is a silyl ketene acetal type compound represented by the following general formula (1), or a partially hydrolyzed condensate thereof, that is, a siloxane produced by further condensing silanol groups generated by partial hydrolysis. used. Moreover, you may use together a silyl ketene acetal type compound and its partial hydrolysis-condensation product.

（式中、Ｒ、Ｒ¹及びＲ²は、置換又は非置換の炭素原子数１〜１２の一価炭化水素基であり、同一でも異なっていてもよく、ｎは１〜６の整数、ａは１〜３の整数を示す。）

Wherein R, R ¹ and R ² are substituted or unsubstituted monovalent hydrocarbon groups having 1 to 12 carbon atoms, which may be the same or different, and n is an integer of 1 to 6, a Represents an integer of 1 to 3.)

In the general formula (1), the monovalent hydrocarbon group having 1 to 12 carbon atoms of R, R ¹ and R ² may be linear, cyclic or branched, such as a methyl group, an ethyl group, Linear alkyl groups such as propyl group, n-butyl group, hexyl group, heptyl group, octyl group, nonyl group and decyl group, cyclic alkyl groups such as cyclohexyl group, and branched structures such as t-butyl group and 2-ethylhexyl group Alkyl groups and halogen-substituted monovalent hydrocarbon groups such as chloromethyl groups, bromoethyl groups, and trifluoropropyl groups in which some or all of the hydrogen atoms of these groups are substituted with halogen atoms such as chlorine, fluorine, and bromine Examples thereof include a substituted group. These groups may be the same or different. In the present invention, preferable R and R ¹ are a methyl group and an ethyl group, and preferable R ² is a methyl group, an ethyl group, an n-butyl group, and a 2-ethylhexyl group.
N is an integer of 1 to 6, preferably 2 to 4, and a is an integer of 1 to 3, preferably 2 or 3.

  The organosilicon compound of the present invention represented by the general formula (1) has a silyl ketene acetal structure in which the silicon-oxygen bond is cleaved under relatively mild conditions. Reacts efficiently with silanols. Therefore, this organosilicon compound is an alcohol-free type RTV as an industrially useful terminal alkoxysilylating agent of organopolysiloxane such as α, ω-dihydroxypolydimethylsiloxane, or as a scavenger for silica surface treatment agent, alcohol, etc. Useful for applications such as storage stabilizers. Moreover, when it has three methoxy groups in a molecule | numerator, since it is a trifunctional alkoxysilane, it is useful also as a hardener of dealcohol type RTV.

〔式中、Ｒ、Ｒ¹、Ｒ²、ｎ、ａは前記の通りである。〕 The silyl ketene acetal type compound of the present invention can be produced by reacting acrylic esters with hydroalkoxysiloxanes. This reaction formula is represented, for example, by the following formula (4).

[Wherein, R, R ¹ , R ² , n, and a are as defined above. ]

  This reaction is a 1,4-addition reaction of the hydrosilyl (SiH) group of the siloxane compound to the acrylate ester, as is apparent from the above formula (4). In this case, in the present invention, as the hydrosiloxane compound, those shown below are preferably used.

（式中、Ｍｅはメチル基、Ｅｔはエチル基を示す。）

(In the formula, Me represents a methyl group, and Et represents an ethyl group.)

  On the other hand, methyl acrylate, ethyl acrylate, n-butyl acrylate, 2-ethylhexyl acrylate, and the like can be preferably used as the acrylic ester used by reacting with the hydrosiloxane compound.

  The amount of the hydrosiloxane compound and acrylic acid ester used in the present invention is preferably 0.8 to 1.2 mol of acrylic acid ester with respect to 1 mol of the hydrosiloxane compound.

  The above reaction is usually carried out in the presence of this type of addition reaction catalyst. Such catalysts include platinum group metal catalysts such as platinum, palladium and rhodium, with platinum being particularly preferred. Examples of the platinum-based material include platinum black or alumina, silica, etc. supported on solid platinum, chloroplatinic acid, alcohol-modified chloroplatinic acid, a complex of chloroplatinic acid and olefin, or platinum and vinylsiloxane. And the like can be exemplified. The amount of these catalysts used may be a so-called catalytic amount, for example, 0.1 to 1,000 ppm, particularly 0.5 to 0.5 ppm in terms of platinum group metal, based on the total amount of the acrylate ester and hydroalkoxysiloxane. Used in an amount of 100 ppm.

  This reaction is generally preferably carried out at a temperature of 50 to 120 ° C., particularly 60 to 100 ° C., for 0.5 to 12 hours, particularly 1 to 6 hours, and can be carried out without using a solvent. As long as the addition reaction is not adversely affected, an appropriate solvent such as toluene or xylene can be used if necessary.

〔式中、Ｒ、Ｒ¹、Ｒ²、ｎ、ａは前記の通りである。〕 In addition, according to the reaction of the above formula (4), in addition to the organosilicon compound of the present invention, the isomers represented by the following formulas (5) and (6) are very slightly produced as side reaction products.

[Wherein, R, R ¹ , R ² , n, and a are as defined above. ]

  The amount of these side reaction products produced is very small, and is an isomer of the organosilicon compound of the present invention, which does not adversely affect the properties thereof, and therefore can be used without separation.

Moreover, this silyl ketene acetal type compound is highly active also with respect to alcohol, and capture | acquires alcohol by reaction as shown in following formula (7). In the following formula, R ′ is a monovalent hydrocarbon group such as a methyl group, and R, R ¹ and R ² are groups as described above.

  Therefore, the silyl ketene acetal type compound is contained in the (A) component diorganopolysiloxane or the alcohol produced by the reaction with the alkoxy group of the silyl ketene acetal type compound itself and the (C) component filler. Since it can capture moisture effectively, it exhibits an excellent effect as a storage stabilizer. Moreover, the alkoxysilane and ester compound produced | generated by the said reaction do not have a bad influence on the sclerosis | hardenability etc. of a composition.

  Furthermore, the silyl ketene acetal type compound as the component (B) has a high boiling point and is difficult to volatilize. That is, since the component (B) acts not only as a curing agent but also as a storage stabilizer, the composition of the present invention is cured even when used as an insulating material or an adhesive around a contact member for electric and electronic devices. It is possible to effectively prevent the problem of contact failure caused by the volatilization of the agent and the storage stabilizer.

  The amount of component (B) is such that the reaction with the alcohol represented by formula (7) proceeds easily and stoichiometrically, so that the silyl ketene acetal type compound is usually equimolar or more with respect to the alcohol. The amount to be. In general, it is preferably blended in an amount of 0.1 to 30 parts by mass, particularly 0.5 to 20 parts by mass per 100 parts by mass of the component (A). If the amount is less than 0.1 parts by mass, the alcohol may remain and the storage stability may be impaired. Even if the amount is more than 30 parts by mass, no further improvement in the effect can be expected, which is economically disadvantageous.

[Component (C)]
Component (C) is a filler and is used to give sufficient mechanical strength to the cured product formed from this composition. Known fillers can be used, for example, fine powder silica, fumed silica, silica aerogel, precipitated silica, diatomaceous earth, iron oxide, zinc oxide, titanium oxide, or other metal oxides, or these Surface treated with silane, metal carbonate such as calcium carbonate, magnesium carbonate, zinc carbonate, asbestos, glass wool, carbon black, fine mica, fused silica powder, synthetic resin powder such as polystyrene, polyvinyl chloride, polypropylene, etc. Is used.

  The blending amount of the filler is preferably 1 to 400 parts by weight, particularly 5 to 200 parts by weight, per 100 parts by weight of the component (A). If the amount is less than 1 part by mass, the cured product obtained from the composition tends not to exhibit sufficient mechanical strength. If the amount is more than 400 parts by mass, the viscosity of the composition increases and the workability is increased. Not only becomes worse, but also the rubber strength after curing tends to be lowered, making it difficult to obtain rubber elasticity.

[(D) component]
Component (D) is an organometallic catalyst and is used to cure the composition. Examples of organometallic catalysts include alkyltin ester compounds such as dibutyltin diacetate, dibutyltin dilaurate, and dibutyltin dioctoate, tetraisopropoxy titanium, tetra n-butoxy titanium, tetrakis (2-ethylhexoxy) titanium, dipropoxy bis (acetylacetate). Nato) titanate or titanium chelate compounds such as titanium, titanium isopropoxyoctylene glycol, zinc naphthenate, zinc stearate, zinc-2-ethyl octoate, iron-2-ethylhexoate, cobalt-2-ethyl Organometallic compounds such as hexoate, manganese-2-ethylhexoate, cobalt naphthenate, alkoxyaluminum compounds, 3-aminopropyltriethoxysilane, N-β (aminoethyl) γ-aminopropyltrime Aminoalkyl group-substituted alkoxysilanes such as toxisilane, amine compounds such as hexylamine and dodecylamine phosphate and salts thereof, quaternary ammonium salts such as benzyltriethylammonium acetate, alkali metals such as potassium acetate, sodium acetate and lithium oxalate Lower fatty acid salt of dimethyldihydroxylamine such as dimethylhydroxylamine, diethylhydroxylamine, tetramethylguanidylpropyltrimethoxysilane, tetramethylguanidylpropylmethyldimethoxysilane, tetramethylguanidylpropyltris (trimethylsiloxy) silane Examples thereof include silane or siloxane containing guanidyl groups such as, but these are not limited to one type, and may be used as a mixture of two or more types.
In addition, the compounding quantity of these curing catalysts is 0.001-15 mass parts with respect to 100 mass parts of organopolysiloxane of the said (A) component, Especially 0.01-5 mass parts is preferable.

  In addition, the room temperature curable organopolysiloxane composition of the present invention includes, as additives, known additives such as pigments, dyes, anti-aging agents, antioxidants, antistatic agents, antimony oxides, flame retardants such as paraffin chloride, and the like. Can be blended. Furthermore, a polyether as a thixotropy improver, a fungicide, an antibacterial agent, and an adhesion aid can be blended.

  Adhesion aids include aminosilanes such as γ-aminopropyltriethoxysilane, 3-2- (aminoethylamino) propyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, and β- (3,4- It is preferable to blend epoxy silanes such as (epoxycyclohexyl) ethyltrimethoxysilane, isocyanate silanes and the like. These adhesion assistants are preferably 0.1 to 20 parts by mass, particularly preferably 0.2 to 10 parts by mass with respect to 100 parts by mass of the organopolysiloxane of component (A).

The organopolysiloxane composition of the present invention can be obtained by uniformly mixing the above-mentioned components and further predetermined amounts of the above-mentioned various additives in a dry atmosphere.
Moreover, although the said organopolysiloxane composition hardens | cures by leaving to stand at room temperature, the well-known method and conditions according to the kind of composition can be employ | adopted for the shaping | molding method, hardening conditions, etc.

  The room temperature curable organopolysiloxane composition of the present invention thus obtained is rapidly cured at room temperature due to moisture in the air, and is excellent in heat resistance, weather resistance, low temperature characteristics, various substrates, particularly adhesion to metals. A rubber elastic body cured product is formed. In addition, this composition is particularly excellent in storage stability and curability, and for example, when it is exposed to the air after storage for 6 months, it rapidly cures to give a cured product having excellent physical properties as described above. In particular, no toxic or corrosive gas is emitted during curing, and no rust is produced on the surface to which this composition is applied. In particular, this composition does not cause contact failure of electrical and electronic parts, so it is useful as an insulating material and adhesive for electrical and electronic parts, as well as a sealing agent, caulking agent, coating agent, mold release agent for various substrates. It can be widely used as a treating agent and a fiber treating agent.

  EXAMPLES Hereinafter, although an Example and a comparative example are shown and this invention is demonstrated concretely, this invention is not restrict | limited to the following Example. In the following specific examples, “part” means “part by mass”, and the viscosity is a value measured by a rotational viscometer at 25 ° C.

（式中、Ｍｅはメチル基、Ｅｔはエチル基である。） [Example 1]
90 parts of dimethylpolysiloxane having both ends of the molecular chain having a viscosity of 20,000 mPa · s blocked with hydroxyl groups and 10 parts of fumed silica whose surface is treated with dimethyldichlorosilane are uniformly mixed, and this is represented by the following formula: A composition was prepared by mixing 8 parts of a silyl ketene acetal type compound and 0.3 part of dibutyltin dilaurate under moisture blocking until uniform.

(In the formula, Me is a methyl group, and Et is an ethyl group.)

[Example 2]
To the composition of Example 1, 1 part of γ-aminopropyltriethoxysilane was further added and mixed under moisture blocking until uniform, to prepare a composition.

[Example 3]
Surface treatment with 35 parts of dimethylpolysiloxane blocked at both ends of molecular chain with viscosity of 50,000 mPa · s with hydroxyl groups, 25 parts of dimethylpolysiloxane blocked at both ends of molecular chain with viscosity of 100 mPa · s with trimethylsiloxy groups, and fatty acid 40 parts of light calcium carbonate (Shiraka Hana CCR, manufactured by Shiraishi Kogyo Co., Ltd.) were mixed uniformly, and 8 parts of a silyl ketene acetal type compound represented by the above formula, 0.3 part of dibutyltin dilaurate, γ-amino A composition was prepared by mixing 1 part of propyltriethoxysilane under moisture blocking until uniform.

[Comparative Example 1]
A composition was prepared in the same manner as in Example 1 except that 4 parts of methyltrimethoxysilane was used instead of 8 parts of the silyl ketene acetal type compound.

[Comparative Example 2]
A composition was prepared in the same manner as in Example 1 except that 6 parts of ethyl 2-trimethoxysilylpropionate was used instead of 8 parts of the silyl ketene acetal type compound.

Next, each composition immediately after preparation prepared in each Example and Comparative Example was extruded into a sheet having a thickness of 2 mm, exposed to air at 23 ° C. and 50% RH, and then the sheet was subjected to 7 under the same atmosphere. The physical properties (initial physical properties) of the cured product obtained after being allowed to stand for days were measured according to JIS K-6249. In addition, hardness was measured using the durometer A hardness meter of JIS K-6249.
Further, this cured product was measured in the same manner as that stored for 100 hours in a constant temperature and humidity chamber at 85 ° C. and 85% RH. Also, each composition prepared in each example and comparative example was placed in a sealed container and allowed to stand for 7 days at a temperature of 70 ° C. The same measurement was performed on a 2 mm long sheet.
These results are shown in Table 1.

[Reference example]
The production method of the silyl ketene acetal type compound shown in Example 1 is as follows.
In a 500 ml four-necked flask equipped with a stirrer, a reflux condenser, a thermometer and a dropping funnel, 100.12 g (1 mol) of ethyl acrylate, 0.23 g of chloroplatinic acid (H ₂ PtCl ₆ .6H ₂ O), Irganox 1330 (Ciba-Geigi Co., Ltd. polymerization inhibitor) 1.4 g, 2,6-di-t-butyl-4-methylphenol (Ciba-Gaigi Co., Ltd. polymerization inhibitor) 1.4 g was added, and stirred. The temperature was raised to 70 ° C.
Next, when 282.5 g (1 mole) of the following hydrosiloxane compound-1 was added dropwise with stirring, an exotherm was observed, the reaction temperature became 70 to 80 ° C., and the reaction system was maintained at this temperature for 4 hours. did. After completion of the reaction, a fraction of 314 g (yield 82%) was obtained at a boiling point of 130 to 132 ° C./7 mmHg by distillation under reduced pressure.
According to gas chromatography (GC) analysis, this fraction was confirmed to contain 97% or more of the desired product (1). ¹ HNMR, ¹³ CNMR and ²⁹ SiNMR charts of the obtained product (1) are shown in FIGS. An IR analysis chart is shown in FIG.

（式中、Ｍｅはメチル基である。）
目的生成物（１）

（式中、Ｍｅはメチル基、Ｅｔはエチル基である。） Hydrosiloxane compound-1

(In the formula, Me is a methyl group.)
Target product (1)

(In the formula, Me is a methyl group, and Et is an ethyl group.)

1 is a ¹ HNMR chart of a target product (1) obtained in Reference Example. It is a ¹³ CNMR chart of the target product (1) obtained in Reference Example. It is a ²⁹ SiNMR chart of the target product (1) obtained in the reference example. It is IR analysis chart of the target product (1) obtained by the reference example.

Claims (4)

(A) a diorganopolysiloxane having a hydroxyl group or hydrolyzable group bonded to at least two silicon atoms in the molecule;
(B) The following general formula (1)

Wherein R, R ¹ and R ² are substituted or unsubstituted monovalent hydrocarbon groups having 1 to 12 carbon atoms, which may be the same or different, and n is an integer of 1 to 6, a Represents an integer of 1 to 3.)
A room temperature-curable organopolysiloxane composition comprising a silyl ketene acetal type compound represented by the formula, a partially hydrolyzed condensate thereof, or a mixture thereof. The room temperature-curable organopolysiloxane composition according to claim 1, wherein the diorganopolysiloxane of component (A) is represented by the following general formula (2) and / or (3).

Wherein R is a substituted or unsubstituted monovalent hydrocarbon group having 1 to 12 carbon atoms, X is an oxygen atom or a divalent hydrocarbon group having 1 to 8 carbon atoms, and m is this diorgano (This is a number that sets the viscosity of polysiloxane at 25 ° C. to 100 to 1,000,000 mPa · s.)

(In the formula, R is a substituted or unsubstituted monovalent hydrocarbon group having 1 to 12 carbon atoms, X is an oxygen atom or a divalent hydrocarbon group having 1 to 8 carbon atoms, and Y is hydrolyzable. And b is 2 or 3, and m is a number that makes the viscosity of this diorganopolysiloxane at 25 ° C. 100 to 1,000,000 mPa · s.)   The room temperature-curable organopolysiloxane composition according to claim 1 or 2, further comprising (C) a filler.   The room temperature-curable organopolysiloxane composition according to claim 1, 2 or 3, further comprising (D) an organometallic catalyst.

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