JP5643614B2 - Curable composition and cured product - Google Patents

Description

  The present invention relates to a curable composition containing a saturated hydrocarbon polymer having a (meth) acryloyl group, a (meth) acrylic monomer, and a polymerization initiator, and a cured product thereof.

  As a sealing material for protecting an electronic material such as an organic light-emitting element or a light-receiving element, whose performance is likely to deteriorate due to exposure to heat or moisture, for example, a photo-curing property such as (Patent Document 1). Epoxy adhesive is used. However, the cured product of the epoxy adhesive is hard, and there are problems in reliability such as generation of cracks due to residual pressure at the time of curing and peeling at the adhesion surface during the thermal test. There is also a method of softening the epoxy cured product, but in this case, there is a problem that the moisture permeability resistance is lowered.

  On the other hand, a saturated hydrocarbon polymer having a reactive functional group at the end exhibits excellent curability by active energy rays and heat, and the resulting cured product may exhibit excellent flexibility and moisture permeability. Are known. For example, (Patent Document 2) discloses a method for producing a saturated hydrocarbon polymer having a cation-reactive epoxy functional group at a molecular end and a curable composition. Although this cured product has an excellent balance between moisture permeability resistance and flexibility, there is room for further improvement in rapid curability.

  In addition, (Patent Document 3) and (Patent Document 4) disclose a method for producing a hydrocarbon polymer having a radical-reactive (meth) acryloyl functional group at the molecular terminal and a curable composition. Although these compositions can be rapidly cured, there is room for further improvement in workability because of their high viscosity.

Japanese Patent Laid-Open No. 2005-41925 WO2005 / 028537 Japanese Patent Laid-Open No. 2-088614 JP 2001-31714 A

  The present invention relates to a curable composition containing a saturated hydrocarbon polymer having a (meth) acryloyl group, a specific (meth) acrylic monomer, and a polymerization initiator and a cured product thereof, and a low viscosity curable composition. An object is to provide a cured product having flexibility and flexibility and moisture permeability.

  As a result of intensive studies to solve the above problems, the present inventors have found the following and completed the present invention.

That is, the present invention
General formula (1):
—Z—C (═O) —NH—R ² —O—C (═O) —C (R ¹ ) ═CH ₂ (1)
(Wherein R ¹ is a hydrogen atom or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms, R ² is a divalent organic group, Z is a heteroatom, NR ³ (R ³ is a hydrogen atom) A saturated hydrocarbon polymer having an average of one or more substituents in the molecule represented by the following formula: atoms or substituted or unsubstituted hydrocarbon groups having 1 to 20 carbon atoms) (A),
General formula (2)
R ⁴ —O—C (═O) —C (R ⁵ ) ═CH ₂ (2)
(Wherein R ⁴ is a group selected from substituted or unsubstituted aliphatic and / or alicyclic hydrocarbon groups having 4 to 20 carbon atoms, R ⁵ is a hydrogen atom, or substituted or unsubstituted carbon. A (meth) acrylic monomer (B) having one (meth) acryloyl group in the molecule represented by (a group selected from hydrocarbon groups having 1 to 20 atoms), and a polymerization initiator (C ) Containing the curable composition.

  The saturated hydrocarbon polymer (A) is preferably an isobutylene polymer.

R ^{1 in the} general formula (1) is preferably a hydrogen atom or a methyl group, and more preferably a hydrogen atom.

  The substituent represented by the general formula (1) preferably has only at the terminal of the saturated hydrocarbon polymer (A).

  The polymerization initiator (C) is preferably a photo radical initiator that generates radicals by light.

  It is preferable that 50 to 200 parts by weight of the (meth) acrylic monomer (B) and 0.001 to 10 parts by weight of the polymerization initiator (C) are included with respect to 100 parts by weight of the saturated hydrocarbon polymer (A). .

The saturated hydrocarbon polymer (A) has the same main chain skeleton as (A) and has a hydroxyl group at the terminal and the saturated hydrocarbon polymer (a) and the general formula (3):
^{O = C = N-R 2} -O-C (= O) -C (R 1) = CH 2 (3)
(Wherein R ¹ and R ² are the same as described above) and are preferably obtained by a reaction of an isocyanate compound (D) represented by:

  The saturated hydrocarbon polymer (a) and the isocyanate compound (D) are preferably reacted using the organotin compound (E) as a catalyst.

  The present invention relates to a cured product obtained by curing the curable composition described above.

  According to the present invention, a cured product having excellent flexibility and moisture permeability resistance can be obtained. Moreover, since the curable composition has a low viscosity, improvement in workability can be expected.

  The present invention will be described in detail below.

<Saturated hydrocarbon polymer (A)>
The saturated hydrocarbon polymer (A) of the present invention has the general formula (1):
—Z—C (═O) —NH—R ² —O—C (═O) —C (R ¹ ) ═CH ₂ (1)
(Wherein R ¹ is a hydrogen atom or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms, R ² is a divalent organic group, Z is a heteroatom, NR ³ (R ³ is a hydrogen atom) And an average of one or more substituents represented by (1) or (2) selected from a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms.

R ¹ in the general formula (1) represents a hydrogen atom or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms. As used herein, a substituted hydrocarbon group refers to a group in which a hydrogen atom on a hydrocarbon group is substituted with a group having a hetero atom. R ¹ is not particularly limited, and examples thereof include a hydrogen atom; an alkyl group such as a methyl group and an ethyl group; a cycloalkyl group such as a cyclohexyl group; an aryl group such as a phenyl group; and an aralkyl group such as a benzyl group. Among these, from the availability of raw materials, a hydrogen atom or a methyl group, and a hydrogen atom is more preferable from the viewpoint of the high reactivity of the saturated hydrocarbon polymer (A).

R ² in the general formula (1) is not particularly limited, and examples thereof include alkylene groups such as methylene group, ethylene group, propylene group, and hexylene group; cycloalkylene groups such as cyclobutylene group, cyclopentylene group, and cyclohexylene group. Groups; arylene groups such as a phenylene group and a benzylene group; and divalent organic groups including an ether bond, an ester bond, an amino bond, an amide bond, and the like. Among these, ethylene group and hexylene group are preferable and ethylene group is more preferable because of easy introduction.

Z in the general formula (1) is not particularly limited, and examples thereof include an oxygen group; a sulfur atom; and an amino group such as —NH— and —NCH ₃ —. In these, an oxygen atom and -NH- group are preferable from the ease of introduction | transduction, and an oxygen atom is more preferable.

  The main chain of the saturated hydrocarbon polymer (A) does not contain a carbon-carbon unsaturated bond other than an aromatic ring, and its skeleton has (1) the number of carbon atoms such as ethylene, propylene, 1-butene and isobutylene. A method of polymerizing 2 to 6 olefinic compounds as main monomers, (2) A method of homopolymerizing diene compounds such as butadiene and isoprene, or copolymerizing the olefinic compounds and then adding hydrogen Etc. can be obtained. Of these, isobutylene-based polymers and hydrogenated polybutadiene-based polymers are preferable because they can easily introduce functional groups at the terminals, easily control the molecular weight, and can increase the number of terminal functional groups. An isobutylene polymer is more preferable. Those whose main chain skeleton is a saturated hydrocarbon polymer have excellent heat resistance, weather resistance, durability, and moisture permeability resistance.

  In the isobutylene-based polymer, all of the repeating units may be formed from isobutylene units or may be a copolymer with other repeating units, but from the viewpoint of rubber properties, the repeating unit derived from isobutylene is 50 wt. % Or more are preferable, those having 80% by weight or more are more preferable, and those having 90 to 99% by weight are particularly preferable.

  The number of (meth) acryloyl substituents in the saturated hydrocarbon polymer (A) is not particularly limited, but from the point that the saturated hydrocarbon polymers (A) are cross-linked, an average of less than one per molecule. Since there exists a tendency for sclerosis | hardenability to become low, one or more is preferable on average. However, for the saturated hydrocarbon polymer (A) having an average of 1 or more (meth) acryloyl substituents per molecule, an average of 1 per molecule is used to adjust the hardness and flexibility of the cured product. A saturated hydrocarbon polymer having less than (meth) acryloyl substituents may be added. Further, the (meth) acryloyl group may be present at any of the side chain and / or the terminal of the molecule, but is preferably present at the terminal of the molecule from the viewpoint of rubber elasticity.

  As a number average molecular weight of a saturated hydrocarbon type polymer (A), 500-50,000 are preferable and 2,000-30,000 are more preferable. When the molecular weight is larger than this, the workability tends to be lowered, and when the molecular weight is small, the characteristics of the main chain skeleton tend to be hardly exhibited.

  The method for synthesizing the saturated hydrocarbon polymer (A) is not particularly limited, and various conventionally reported polymerization methods may be mentioned, but the living polymerization method that has been reported in many recent years is particularly preferable. Of these, in the case of saturated hydrocarbon polymers, particularly isobutylene polymers, inifer polymerization discovered by Kennedy et al. (JP Kennedy et al., J. Polymer Sci., Polymer Chem. Ed. 1997). 15, page 2843), and can be polymerized with a molecular weight of about 500 to 100,000 with a molecular weight distribution of 1.5 or less, and various functional groups can be introduced at the molecular ends. Are known.

The saturated hydrocarbon polymer (A) of the present invention has the same main chain skeleton as the saturated hydrocarbon polymer (A), and has a hydroxyl group, an amino group, and a thiol group at the terminal. And general formula (3):
^{O = C = N-R 2} -O-C (= O) -C (R 1) = CH 2 (3)
(Wherein R ¹ and R ² are the same as described above) are preferably obtained by reacting, and a saturated hydrocarbon polymer (a) having a hydroxyl group at the terminal is used. It is more preferable.

  The main chain of the saturated hydrocarbon polymer (a) is, for example, the above-mentioned J.M. P. It can be obtained by the method of Kennedy et al. The saturated hydrocarbon polymer (a) includes a halogen-terminated saturated hydrocarbon polymer (a) obtained by cationic polymerization forming a carbon-carbon single bond, a protected hydroxyl group, and a carbon-carbon double bond. It can be obtained by reacting the compound (ii) having a deprotection to deprotect the hydroxyl group.

The halogen-terminated saturated hydrocarbon polymer (A) is represented by the general formula (4):
R ⁶ (AX) _a (4)
(In the formula, R ⁶ is a monocyclic or monovalent to tetravalent hydrocarbon group containing a plurality of aromatic rings, X is a chlorine atom or a bromine atom, and a is an integer of 1 to 4. Is a polymer of one kind or two or more kinds of cationically polymerizable monomers, and when a is 2 or more, they may be the same or different.

  The cationically polymerizable monomer in the general formula (4) is not particularly limited, but preferred examples include isobutylene, indene, pinene, styrene, methoxystyrene, chlorostyrene and the like. Of these, isobutylene is preferred for the above reasons.

  Moreover, when obtaining hardened | cured material by bridge | crosslinking reaction, in order to achieve sufficient intensity | strength, a weather resistance, a gel fraction, etc., it is preferable that a in General formula (4) is 2 or 3.

The compound (b) having a protected hydroxyl group and a carbon-carbon double bond is represented by the general formula (5):
_{^{CH 2 = C (R 7)}} -R 8 -OG (5)
(Wherein R ⁷ represents a hydrogen atom or a saturated hydrocarbon group having 1 to 18 carbon atoms, R ⁸ represents a hydrocarbon group having 1 to 30 carbon atoms, and G represents a protecting group for a hydroxyl group). Is done. R ⁸ in the general formula (5) is a hydrocarbon group having 1 to 30 carbon atoms, and is 0 to 5 carbon-carbon double bonds and / or 0 to 3 aromatic rings. And more preferably 0 to 3 —CH═CH— groups.

As a compound of general formula (5), general formula (6):
^{_{CH 2 = C (R 7)}} - (CH 2) b - {- CH = CH- (CH 2) c} n -OG (6)
(In the formula, R ⁷ is the same as described above. G represents a protecting group for a hydroxyl group, and n represents an integer of 0 to 5. b and c are integers of 1 to 30, which may be the same or different. It is more preferable that it is a compound represented by.

  The protecting group of the compound (b) is not particularly limited as long as it provides a hydroxyl group by deprotection, but is usually an inorganic substituent having 0 to 54 carbon atoms or an organic substituent. It is. Moreover, it is preferable that deprotection can be performed under mild conditions, and preferable protective groups include the following.

（式中、Ｒ'、Ｒ''、Ｒ'''は水素原子、または、炭素原子数１から１８の飽和または不飽和の炭化水素基を表わし、Ｒを複数含む基においては、同一であっても異なっていても良い。Ｘ’はＣｌ、Ｂｒ、Ｉから選ばれる官能基である。ＭはＬｉ、Ｎａ、Ｋから選ばれる１価の金属、Ｍ'はＭｇ、Ｃａ、Ｓｒ、Ｂａから選ばれる２価の金属、Ｍ''はＢ、Ａｌ、Ｇａから選ばれる３価の金属、Ｍ'''はＴｉ、Ｚｒ、Ｈｆ、Ｓｉ、Ｇｅ、Ｓｎ、Ｐｂから選ばれる４価の金属を表わす。）
入手性や脱保護後の重合体と保護基成分の分離のし易さなどから、アルキル基、アシル基、ＲＣ（＝Ｏ）−基（ただし、Ｒは炭素数１から１０の飽和炭化水素基）、シリル基、金属アルコキシドが好ましく、メチル基、エチル基、ｎ−プロピル基、ｉｓｏ−プロピル基、ｎ−ブチル基、ｓｅｃ−ブチル基、ｔｅｒｔ−ブチル基、ホルミル基、アセチル基、プロピオニル基、ブチリル基、ベンゾイル基、トリメチルシリル基、トリフェニルシリル基がさらに好ましい。

(In the formula, R ′, R ″, and R ′ ″ represent a hydrogen atom or a saturated or unsaturated hydrocarbon group having 1 to 18 carbon atoms. X ′ is a functional group selected from Cl, Br, and I. M is a monovalent metal selected from Li, Na, and K, and M ′ is selected from Mg, Ca, Sr, and Ba. Divalent metal selected, M ″ is a trivalent metal selected from B, Al, and Ga, and M ′ ″ is a tetravalent metal selected from Ti, Zr, Hf, Si, Ge, Sn, and Pb. Represents.)
Alkyl group, acyl group, RC (═O) — group (where R is a saturated hydrocarbon group having 1 to 10 carbon atoms) due to availability and ease of separation of polymer and protecting group component after deprotection ), Silyl group and metal alkoxide are preferred, methyl group, ethyl group, n-propyl group, iso-propyl group, n-butyl group, sec-butyl group, tert-butyl group, formyl group, acetyl group, propionyl group, A butyryl group, a benzoyl group, a trimethylsilyl group, and a triphenylsilyl group are more preferable.

  The compound (b), which is a substrate to be reacted with the halogen-terminated saturated hydrocarbon polymer (a), is not particularly limited as long as it is an olefin having a hydroxyl group protected at the terminal of 1-substitution or 1,1′-2 substitution. However, due to its high reactivity, when G in formula (5) is hydrogen, allyl alcohol, methallyl alcohol, 3-buten-1-ol, 3-methyl-3-butene -1-ol, 4-penten-1-ol, 5-hexen-1-ol, 6-hepten-1-ol, 7-octen-1-ol, 8-nonen-1-ol, 9-decene-1 -Ol and 10-undecen-1-ol, 2,5-hexadienol, 2,6-heptadienol, 3,6-heptadienol, 2,7-octadienol, 3,7-octa Dienol, 4, -Octadienol, 2,8-nonadienol, 3,8-nonadienol, 4,8-nonadienol, 5,8-nonadienol, 2,9-decadienol, 3,9-decadienol, 4,9-decadienol, 5,9 A compound selected from -decadienol or 6,9-decadienol is preferred.

When the compound (b) is reacted with the halogen-terminated saturated hydrocarbon polymer (a), a Lewis acid can be used as a catalyst. The Lewis acid is not particularly limited, but TiCl ₄ , AlCl ₃ , BCl ₃ , and SnCl ₄ are preferable from the viewpoint of high activity and good selectivity.

  When the halogen-terminated saturated hydrocarbon polymer (a) is polymerized or the compound (b) is reacted with the halogen-terminated saturated hydrocarbon polymer (a), a halogenated hydrocarbon, an aromatic hydrocarbon, and In addition, a single solvent or a mixed solvent selected from aliphatic hydrocarbons can be used. Among halogenated hydrocarbons, methylene chloride, chloroform, 1,1-dichloroethane, 1,2-dichloroethane, n-propyl chloride, and n-butyl chloride from the viewpoint of solubility and reactivity under polymerization conditions of the polymer. It is preferable that it is 1 or more types of components chosen from these. For the same reason, the aromatic hydrocarbon is preferably toluene, and the aliphatic hydrocarbon is preferably one or more components selected from pentane, n-hexane, cyclohexane, methylcyclohexane, and ethylcyclohexane.

  Examples of solvents that do not use halogenated hydrocarbons that may be harmful to the environment include, for example, toluene, ethylcyclohexane, or saturated hydrocarbons having terminal hydroxyl groups protected by using mixed solvents thereof. Production of a polymer can be easily achieved.

  The deprotection reaction is not particularly limited as long as it is a reaction that induces a protecting group to a hydroxyl group, but preferred reactions include hydrolysis reaction, thermal decomposition reaction and the like.

  The hydrolysis reaction can be carried out either in a solvent system or in a solventless system. The solvent used for the solvent-based reaction is not particularly limited, but a solvent for producing a saturated hydrocarbon polymer having a protected hydroxyl group at the terminal is preferably used. As the conditions for the hydrolysis, either acidic or basic conditions are possible, but it is preferable to perform the hydrolysis reaction using a basic aqueous solution in view of the efficiency of the hydrolysis reaction.

  The reagent used for the hydrolysis reaction under basic conditions is not particularly limited as long as it is an organic or inorganic basic compound used for a normal hydrolysis reaction. Sodium, potassium hydroxide, lithium hydroxide, calcium hydroxide, magnesium hydroxide, sodium carbonate, potassium carbonate, lithium carbonate, calcium carbonate, magnesium carbonate, sodium acetate, potassium acetate, lithium acetate, calcium acetate, magnesium acetate, tert- Preferred are butoxy potassium, tert-butoxy sodium, potassium methoxide, sodium methoxide and the like.

  In the hydrolysis reaction, the reaction can be efficiently advanced by adding a catalyst. As such a catalyst, any of organic and inorganic catalysts can be used. From the viewpoint of reactivity, an organic salt is preferable, and a quaternary ammonium salt is particularly preferable. Representative ammonium salts include triethylbenzylammonium chloride, tetramethylammonium chloride, triethylbenzylammonium bromide, trioctylmethylammonium chloride, tributylbenzylammonium chloride, trimethylbenzylammonium chloride, N-laurylpyridinium chloride, tetrahydroxide hydroxide n-butylammonium hydroxide, tetramethylammonium hydroxide, trimethylbenzylammonium hydroxide, trimethylphenylammonium bromide, tetramethylammonium bromide, tetraethylammonium bromide, tetra-n-butylammonium bromide, tetrabutylammonium hydrogen sulfate, N -Benzylpicolinium chloride, tetramethylammonium iodide, iodo-tetra-n-butylammonium, - lauryl-4-picolinium chloride, etc. N- laurylpicolinium chloride and the like.

The same thing as R < ¹ >, R < ² > in General formula (1) can be said as R < ¹ >, R < ² > of the isocyanate type compound (D) represented by General formula (4).

  Although it does not restrict | limit especially as an isocyanate type compound (B), The following compound can be mentioned.

  Of these, 2-acryloyloxyethyl isocyanate and 2-methacryloyloxyisocyanate are preferable and 2-acryloyloxyethyl isocyanate is more preferable from the viewpoints of reactivity and availability.

  As usage-amount of an isocyanate type compound (D), 0.1-5 equivalent is preferable with respect to the hydroxyl group of a saturated hydrocarbon type polymer (a), 0.5-1.5 equivalent is more preferable, and is equivalent. More preferably. When the amount used is larger than this, it is economically disadvantageous, and when it is less, the curability of the resulting saturated hydrocarbon polymer (A) tends to be lowered.

  When the saturated hydrocarbon polymer (a) and the isocyanate compound (D) are reacted, a catalyst can be used for the purpose of increasing the reactivity. Although it does not restrict | limit especially as a catalyst, An organotin type compound (E), a titanium type compound, a zirconium type compound, and an amine type compound can be mentioned. Specifically, dibutyltin dilaurate, dibutyltin maleate, dibutyltin phthalate, dibutyltin dioctanoate, dibutyltin bis (2-ethylhexanoate), dibutyltin bis (methyl maleate), dibutyltin bis (ethyl maleate) , Dibutyltin bis (butyl maleate), dibutyltin bis (octylmaleate), dibutyltin bis (tridecylmaleate), dibutyltin bis (benzylmaleate), dibutyltin diacetate, dioctyltin bis (ethylmaleate) ), Dioctyltin bis (octyl maleate), dibutyltin dimethoxide, dibutyltin bis (nonylphenoxide), dibutenyltin oxide, dibutyltin oxide, dibutyltin bis (acetylacetonate), dibutyltin bis (ethylacetoacetona) G), organotin compounds such as reaction product of dibutyltin oxide and silicate compound, reaction product of dibutyltin oxide and phthalate ester; tetrabutyl titanate, tetrapropyl titanate, titanium tetrakis (acetylacetonate), titanium di- Titanium compounds such as isopropoxybis (acetylacetonato), titanium diisopropoxybis (ethyl acetate); zirconium compounds such as zirconium tetrakis (acetylacetonate); triethylamine, triamylamine, trihexylamine, trioctylamine, etc. Aliphatic tertiary amines; aliphatic unsaturated amines such as triallylamine and oleylamine; aromatic amines such as aniline, laurylaniline, stearylaniline, and triphenylamine; pyridine 2-aminopyridine, 2- (dimethylamino) pyridine, 4- (dimethylaminopyridine), 2-hydroxypyridine, imidazole, 2-ethyl-4-methylimidazole, morpholine, N-methylmorpholine, piperidine, 2-piperidinemethanol 2- (2-piperidino) ethanol, piperidone, 1,2-dimethyl-1,4,5,6-tetrahydropyrimidine, 1,8-diazabicyclo (5,4,0) undecene-7 (DBU), 6- (Dibutylamino) -1,8-diazabicyclo (5,4,0) undecene-7 (DBA-DBU), 1,5-diazabicyclo (4,3,0) nonene-5 (DBN), 1,4-diazabicyclo (2,2,2) octane (DABCO), nitrogen-containing heterocyclic compounds such as aziridine, and other amino acids As ethylenes, ethylenediamine, propylenediamine, hexamethylenediamine, N-methyl-1,3-propanediamine, N, N′-dimethyl-1,3-propanediamine, diethylenetriamine, triethylenetetramine, benzylamine, 3-methoxy Such as propylamine, 3-lauryloxypropylamine, 3-dimethylaminopropylamine, 3-diethylaminopropylamine, 3-dibutylaminopropylamine, 3-morpholinopropylamine, 2- (1-piperazinyl) ethylamine, xylylenediamine, etc. Amines; Guanidines such as guanidine, phenylguanidine and diphenylguanidine; and biguanides such as butylbiguanide, 1-o-tolylbiguanide and 1-phenylbiguanide. Among these, from the viewpoint of reactivity, organotin compounds are preferable, and dibutyltin (mercapto acid ester) is particularly preferable.

  As usage-amount of an organic tin type compound (E), 10 ppm-500 ppm are preferable with respect to a saturated hydrocarbon type polymer (a), and 25 ppm-100 ppm are more preferable. If the amount used is larger than this, a by-product may be generated, and if it is smaller than this, a sufficient effect may not be obtained.

  When reacting the saturated hydrocarbon polymer (a) and the isocyanate compound (D), a solvent may or may not be used. When a solvent is used, a solvent in which the saturated hydrocarbon polymer (a) is dissolved is preferable. Although it does not restrict | limit especially as a solvent, For example, toluene, hexane, etc. are mentioned. The amount of the solvent used can be appropriately determined from the viewpoint of easiness of stirring.

<(Meth) acrylic monomer (B)>
The number of (meth) acrylic substituents of the (meth) acrylic monomer (B) is preferably one per molecule from the viewpoint of reducing the viscosity of the curable composition. However, if the monomer (B) having one (meth) acrylic substituent per molecule is included, two or more (meth) acrylic substitutions per molecule are required to adjust the hardness of the cured product. A (meth) acrylic monomer having a group may be included.

The (meth) acrylic monomer (B) preferably has one (meth) acryloyl group listed in the general formula (2) in view of compatibility with the saturated hydrocarbon polymer (A).
R ⁴ —O—C (═O) —C (R ⁵ ) ═CH ₂ (2)
(Wherein R ⁴ is a group selected from substituted or unsubstituted aliphatic and / or alicyclic hydrocarbon groups having 4 to 20 carbon atoms, R ⁵ is a hydrogen atom, or substituted or unsubstituted carbon. This is a group selected from hydrocarbon groups having 1 to 20 atoms.)
R ⁴ in the general formula (2) represents a group selected from a substituted or unsubstituted aliphatic and / or alicyclic hydrocarbon group having 4 to 20 carbon atoms. As used herein, a substituted hydrocarbon group refers to a group in which a hydrogen atom on a hydrocarbon group is substituted with a group having a hetero atom. R ⁵ is not particularly limited, and examples thereof include a hydrogen atom; an alkyl group such as a methyl group and an ethyl group; a cycloalkyl group such as a cyclohexyl group; an aryl group such as a phenyl group; and an aralkyl group such as a benzyl group. Among these, a hydrogen atom or a methyl group is more preferable from the viewpoint of availability of raw materials, and a hydrogen atom is more preferable from the viewpoint of the reactivity of the saturated hydrocarbon polymer (A).
Examples of such (meth) acrylate monomers include, for example, n-butyl (meth) acrylate, isobutyl (meth) acrylate, tert-butyl (meth) acrylate, n-pentyl acrylate, and (meth) acrylate n. -Hexyl, n-heptyl (meth) acrylate, n-octyl (meth) acrylate, isooctyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, n-nonyl (meth) acrylate, (meth) acryl Isononyl acid, n-decyl (meth) acrylate, lauryl (meth) acrylate, n-stearyl (meth) acrylate, isostearyl (meth) acrylate, cyclohexyl (meth) acrylate, benzyl (meth) acrylate, Toluyl (meth) acrylate, isobornyl (meth) acrylate, (meth) acrylic Acid dicyclopentanyl the like. Of these, isobornyl acrylate and lauryl acrylate are preferable in terms of availability, compatibility, and low viscosity of the composition.

  The mixing amount of the (meth) acrylic monomer is not particularly limited, but is preferably 30 parts by weight to 200 parts by weight and more preferably 50 parts by weight to 150 parts with respect to 100 parts by weight of the saturated hydrocarbon polymer (A). When the addition amount of the (meth) acrylic monomer is less than 30 parts by weight, the viscosity of the composition may be high and workability may be deteriorated. When the mixing amount is more than 200 parts by weight, flexibility and permeation resistance are increased. Humidity may be worsened. In addition, when the mixture of a (meth) acrylic acid ester monomer is used, it is preferable that the total amount of a mixture exists in the said range.

<Polymerization initiator (C)>
Although it does not specifically limit as a polymerization initiator (C), The radical initiator which generate | occur | produces a radical by an active energy ray and / or a heat | fever, a photoanion initiator, a redox initiator, etc. are mentioned. In these, the radical initiator which generate | occur | produces a radical by an active energy ray and / or a heat | fever is preferable from a point of availability, and a photoradical initiator is more preferable from a reactive point.

  Although it does not specifically limit as a photoradical initiator, For example, acetophenone, propiophenone, benzophenone, xanthol, fluorin, benzaldehyde, anthraquinone, triphenylamine, carbazole, 3-methylacetophenone, 4-methylacetophenone, 3- Pentylacetophenone, 2,2-diethoxyacetophenone, 4-methoxyacetophene, 3-bromoacetophenone, 4-allylacetophenone, p-diacetylbenzene, 3-methoxybenzophenone, 4-methylbenzophenone, 4-chlorobenzophenone, 4,4 '-Dimethoxybenzophenone, 4-chloro-4'-benzylbenzophenone, 3-chloroxanthone, 3,9-dichloroxanthone, 3-chloro-8-nonylxanthone, Zoyl, benzoin methyl ether, benzoin butyl ether, bis (4-dimethylaminophenyl) ketone, benzylmethoxy ketal, 2-chlorothioxanthone, 2,2-dimethoxy-1,2-diphenylethane-1-one, 1-hydroxy -Cyclohexyl-phenyl-ketone, 2-hydroxy-2-methyl-1-phenyl-propan-1-one, 2-methyl-1- [4- (methylthio) phenyl] -2-morpholinopropan-1-one, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1 and the like. Among these, phenyl ketone compounds are preferred in that they have tack-improving properties.

  In addition, an acylphosphine oxide photopolymerization initiator having excellent deep curability during UV irradiation can also be blended. Acylphosphine oxide polymerization initiators include 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide, bis (2,6-dimethoxybenzoyl) ) -2,4,4-trimethyl-pentylphosphine oxide, bis (2,6-dimethylbenzoyl) -phenylphosphine oxide, bis (2,4,6-trimethylbenzoyl) -isobutylphosphine oxide, bis (2 , 6-dimethoxybenzoyl) -isobutylphosphine oxide, bis (2,6-dimethoxybenzoyl) -phenylphosphine oxide, etc., preferably 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide Bis (2,4,6-trimethylbenzoyl) - phenyl phosphine oxide, bis (2,6-dimethoxybenzoyl) -2,4,4-trimethyl - a pentyl phosphine oxide. The above photo radical initiators may be used alone or in combination of two or more. Among them, because of high reactivity, 1-hydroxy-cyclohexyl-phenyl-ketone, 2-hydroxy-2-methyl-1-phenyl-propan-1-one, 2,2-dimethoxy-1,2-diphenylethane -1-one, 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, and bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide are preferred.

  In the curable composition of the present invention, the acylphosphine oxide and the phenyl ketone compound can be used in combination.

  Although it does not specifically limit as a thermal radical initiator, For example, an azo initiator, a peroxide initiator, a persulfate initiator etc. are mentioned.

  The azo initiator is not particularly limited, and examples thereof include 2,2′-azobis (4-methoxy-2,4-dimethylvaleronitrile), 2,2′-azobis (2-amidinopropane) dihydrochloride, 2,2′-azobis (2,4-dimethylvaleronitrile), 2,2′-azobis (isobutyronitrile), 2,2′-azobis-2-methylbutyronitrile, 1,1-azobis (1 -Cyclohexanecarbonitrile), 2,2'-azobis (2-cyclopropylpropionitrile), 2,2'-azobis (methylisobutyrate) and the like.

  The peroxide initiator is not particularly limited, and examples thereof include benzoyl peroxide, acetyl peroxide, lauroyl peroxide, decanoyl peroxide, dicetyl peroxydicarbonate, and di (4-t-butylcyclohexyl) peroxydi. Examples include carbonate, di (2-ethylhexyl) peroxydicarbonate, t-butylperoxypivalate, t-butylperoxy-2-ethylhexanoate, and dicumyl peroxide.

  Although it does not specifically limit as a persulfate initiator, For example, potassium persulfate, sodium persulfate, ammonium persulfate, etc. are mentioned.

  A thermal radical initiator may be used independently or may use 2 or more types together. Among the above thermal radical initiators, those selected from the group consisting of azo initiators and peroxide initiators are preferable from the viewpoint of ease of handling. Also, because of its high reactivity, 2,2′-azobis (methylisobutyrate), benzoyl peroxide, t-butyl peroxypivalate, di (4-t-butylcyclohexyl) peroxydicarbonate, and These mixtures are more preferred.

  The mixing amount of the radical initiator is not particularly limited regardless of the type, but is preferably 0.001 to 10 parts by weight, and 0.01 parts by weight with respect to 100 parts by weight of the saturated hydrocarbon polymer (A). To 3 parts by weight is more preferable. If the addition amount of the radical initiator is less than this range, sufficient curability may not be obtained, and if the mixing amount exceeds this range, the cured product may be affected. When a mixture of radical initiators is used, the total amount of the mixture is preferably within the above range.

  The photoanion initiator is not particularly limited, and examples thereof include carbamates, amides, amines, imides, oxime esters, α-cobalt complexes, and imidazoles. These may be used alone or in combination of two or more.

  The mixing amount of the photoanion initiator is preferably 0.1 to 10 parts by weight, more preferably 0.3 to 8 parts by weight with respect to 100 parts by weight of the saturated hydrocarbon polymer (A). preferable.

  Redox initiators include, but are not limited to, combinations of the above-described persulfate initiators and reducing agents such as sodium bisulfite; systems based on organic peroxides and tertiary amines such as benzoyl peroxide and dimethyl Systems based on aniline; and systems based on organic hydroperoxides and transition metals, such as systems based on cumene hydroperoxide and cobalt naphthate. These may be used alone or in combination of two or more.

  The mixing amount of the redox initiator is preferably 0.01 to 5 parts by weight, and preferably 0.025 to 2 parts by weight with respect to 100 parts by weight of the saturated hydrocarbon polymer (A).

<Curable composition>
The curable composition of the present invention contains other components such as a radical scavenger, a plasticizer, a silane coupling agent, a filler, a modifier, and other resin components as long as the effects of the present invention are not impaired. can do.
The radical scavenger mentioned here generally includes what are called antioxidants and light stabilizers.

  The antioxidant is not particularly limited, and examples thereof include hindered phenol-based, monophenol-based, bisphenol-based, and polyphenol-based antioxidants. Among these, hindered phenol-based antioxidants are preferable. Similarly, Tinuvin 622LD, Tinuvin 144, CHIMASSORB 944LD, CHIMASSORB 119FL (all of which are manufactured by BASF Corporation); MARK LA-57, MARK LA-62, MARK LA-67, MARK LA-63, MARK LA-68 (above, All are manufactured by ADEKA Corporation); Sanol LS-770, Sanol LS-765, Sanol LS-292, Sanol LS-2626, Sanol LS-1114, Sanol LS-744 (all are manufactured by Sankyo Co., Ltd.) The indicated hindered amine light stabilizers can also be used. Specific examples of the antioxidant are also described in JP-A-4-283259 and JP-A-9-194731. The amount of the antioxidant used is preferably in the range of 0.1 to 10 parts by weight, more preferably 0.2 parts by weight per 100 parts by weight of the saturated hydrocarbon polymer (A). Part to 5 parts by weight. If the amount used is smaller than this, sufficient effects may not be obtained. If the amount used is larger than this, it is not only economically disadvantageous, but also radicals generated from the photo radical initiator. May be supplemented by an antioxidant, resulting in poor curing of the cured product, and the cured product may not exhibit good physical properties.

  Examples of the light stabilizer include benzotriazole, hindered amine, and benzoate compounds. Among these, hindered amine compounds are preferable. The light stabilizer is preferably used in an amount of 0.1 to 10 parts by weight, preferably 0.2 to 5 parts by weight per 100 parts by weight of the saturated hydrocarbon polymer (A). Part is more preferred. If the amount used is smaller than this, sufficient effects may not be obtained. If the amount used is larger than this, it may not only be economically disadvantageous, but also a photo radical initiator. There is a possibility that the antioxidant is supplemented by the generated radicals, and the cured product is poorly cured, and the cured product does not exhibit good physical properties. Specific examples of the light stabilizer are also shown in JP-A-9-194731.

  Examples of plasticizers include phthalates such as dibutyl phthalate, diheptyl phthalate, di (2-ethylhexyl) phthalate, and butyl benzyl phthalate; non-aromatic dibasic esters such as dioctyl adipate and dioctyl sebacate; diethylene glycol dibenzoate Polyalkylene glycol esters such as triethylene glycol dibenzoate; Phosphate esters such as tricresyl phosphate and tributyl phosphate; Chlorinated paraffins; Hydrocarbon oils such as alkyldiphenyl and partially hydrogenated terphenyl alone , Or a mixture of two or more types, but is not necessarily required. In addition, these plasticizers can also be mix | blended at the time of saturated hydrocarbon type polymer manufacture. The amount of the plasticizer used is preferably in the range of 5 to 200 parts by weight, more preferably 10 to 100 parts by weight, with respect to 100 parts by weight of the saturated hydrocarbon polymer (A). When the amount used is less than this, a sufficient effect may not be obtained, and when the amount used is larger than this, the mechanical properties of the obtained cured product may be lowered. The addition of a plasticizer is effective for adjusting physical properties and properties.

  Examples of the silane coupling agent include silane compounds having a reactive group such as an epoxy group, a carboxyl group, a methacryloyl group, and an isocyanate group. Specifically, trimethoxysilylbenzoic acid, γ-methacryloxypropyltrimethoxysilane, vinyltriacetoxysilane, vinyltrimethoxysilane, γ-isocyanatopropyltriethoxysilane, γ-glycidoxypropyltrimethoxysilane, β -(3,4-epoxycyclohexyl) ethyltrimethylsilane and the like. These may be used alone or in combination of two or more. Although the content rate of the silane coupling agent component in the resin composition of the present invention is not particularly limited, it is usually 0.1 with respect to the total of 100 parts by weight of the component (A), the component (B), and the component (C). -20 parts by weight, preferably 0.3-10 parts by weight. Addition of a silane coupling agent is effective for improving adhesiveness and water resistance.

  Examples of the filler include fine particle silica, glass beads, talc, styrene polymer particles, methacrylate polymer particles, ethylene polymer particles, and propylene polymer particles. Among them, inorganic fillers are preferable, and fine particle silica is particularly preferable. preferable. These may be used alone or in combination of two or more. Although the content rate of a filler component does not have limitation in particular, It is 20-150 weight part normally with respect to a total of 100 weight part of (A) component, (B) component, and (C) component, Preferably 50- 100 parts by weight. By adding an inorganic filler, it is possible to improve the strength, moisture permeability resistance and adhesion.

  Examples of the modifier include polymerization initiation assistants, leveling agents, wettability improvers, surfactants, and the like. These may be used alone or in combination of two or more.

  Examples of other resin components include resin components such as polyamide, polyurethane, polybutadiene, polyether, polyester, acrylic resin, silicon resin, and fluorine resin.

<Hardened product>
The curable composition of this invention is prepared by mixing each component uniformly. Although there is no particular limitation on the mixing method, first, the components other than the polymerization initiator of component (C) are sufficiently mixed, and then the polymerization initiator of component (C) is mixed to improve the stability of the composition. This is preferable. In the case of mixing, the apparatus is not particularly limited, but it is prepared by appropriately mixing using a hand stirring, a mechanical stirring apparatus, a roll mill or the like.

  The cured product of the present invention can be cured by active energy rays or heat.

  In the case of curing with active energy rays, the active energy rays include light (UV) or electron beam, and the active energy ray source is not particularly limited, but depends on the properties of the photopolymerization initiator used. Examples thereof include a high pressure mercury lamp, a low pressure mercury lamp, an electron beam irradiation device, a halogen lamp, a light emitting diode, a semiconductor laser, and a metal halide.

  The curing temperature is preferably 0 ° C to 150 ° C, more preferably 5 ° C to 120 ° C. When a redox initiator is used in combination as another initiator, the curing temperature is preferably −50 ° C. to 250 ° C., more preferably 0 ° C. to 180 ° C.

  When cured by heat, the curing temperature is preferably 30 ° C to 200 ° C, more preferably 80 ° C to 180 ° C.

  As the application of the curable composition to be applied when obtaining a cured product, for example, brush coating, extrusion, spraying, gravure, kiss roll, dispenser and air knife, a technique known in the art can be used. Applicable according to characteristics.

  The solid substrate to which the curable composition of the present invention is applied is a flexible sheet material such as paper, polyolefin film, polyolefin coated paper, foil, wood, cardboard and cotton; metal such as aluminum, copper, steel and silver. Materials; siliceous materials such as glass and stone; and synthetic polymers such as polyolefins, polyamides, polyesters and polyacrylates.

  The photocurable composition of the present invention is useful as an adhesive, a paint, a sealant composition, a waterproofing agent, a spraying agent, a molding material, an injection rubber material, and the like. Specific examples include UV curable materials / coating / inks, liquid solder resists, liquid crystal resists, optical fiber coating agents, UV / visible light curable adhesives, optical disk coating agents, and electronic component sealants. Among them, it is useful as a sealant for electronic components such as organic EL and electronic paper, which are required to have moisture permeability resistance and flexibility.

  Hereinafter, the present invention will be described in more detail based on examples, but the present invention is not limited thereby.

  In the following examples, “number average molecular weight” and “molecular weight distribution (ratio of weight average molecular weight to number average molecular weight)” were calculated by a standard polystyrene conversion method using gel permeation chromatography (GPC). However, LC Module 1 manufactured by Waters was used as the GPC system, polystyrene crosslinked gel was used as the GPC column (Shodex GPC K-804; manufactured by Showa Denko KK), and chloroform was used as the GPC solvent.

(Synthesis Example 1)
A 5000 mL separable flask was equipped with a three-way cock, a thermocouple, and a stirrer with a vacuum seal, and was purged with nitrogen. To this, 592 mL of toluene dehydrated by Molecular Sieves 3A and 73.6 mL of ethylcyclohexane were added, and 1,4-bis (1-chloro-1-methylethyl) benzene (5.56 g, 24.0 mmol), 2- Methylpyridine (264 mg, 2.83 mmol) was added and cooled to -70 ° C. After cooling, isobutylene monomer (120 mL, 1.44 mol) was introduced, and further titanium tetrachloride (2.52 mL, 23.0 mmol) was added at this temperature to initiate polymerization. At this time, the temperature was raised by about 15 ° C. Polymerization was completed in about 60 minutes (with this, no exotherm of the reaction system was observed). After completion of the polymerization, 2,7-octadienyl acetate (32.4 g, 193 mmol) and titanium tetrachloride (39.8 mL, 386 mmol) were added. After 5 hours, the reaction mixture was introduced into 1.5 L of ion-exchanged water heated to 80 ° C. and stirred for 20 minutes. After standing, the aqueous layer was removed, 1 L of 2N aqueous sodium hydroxide solution and 10.0 g of tetrabutylammonium bromide were added, and the mixture was stirred at 100 ° C. for 12 hours. After completion of the reaction, the alkaline aqueous solution was removed, and after washing with 1 L of ion exchange water three times, the organic layer was isolated. To this, 10 L of acetone was added to reprecipitate the polymer to remove low molecular weight compounds. The precipitate was washed twice with 1 L of acetone and dissolved in 500 ml of hexane. The solution is transferred to a 1-L flask and the solvent is distilled off under heating conditions (180 ° C.) under reduced pressure (1 Torr or less) using an oil bath to obtain an isobutylene polymer (a) having a target hydroxyl group at the end. (Number average molecular weight 5600, molecular weight distribution 1.2). The functionalization rate of the polymer (a) was calculated using ¹ H NMR (Varian's Gemini-300, measuring solvent = carbon tetrachloride / heavy acetone = 4/1 mixed solvent, quantification method = initiator residue Based on the signal (7.2 ppm), the signal of methylene adjacent to the terminal hydroxyl group (4.00 ppm) was compared and quantified). As a result, the amount of hydroxyl groups introduced into the obtained polymer (a) was 1.2 per molecule.

10 g of isobutylene polymer (a), 15 mL of toluene, and 2 mg of 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxy were added to the flask and devolatilized at 90 ° C. for 2 hours. After devolatilization, 0.44 μL of dibutyltin bis (mercapto ester) (Nitto Kasei Co., Ltd. Neostan U-360), 2-acryloyloxyethyl isocyanate (Karenz AOI, Showa Denko Co., Ltd.) 0.41 g was added, The mixture was stirred at 90 ° C. for 2 hours. This obtained the isobutylene type polymer (A) which has a (meth) acryloyl type substituent at the terminal (number average molecular weight 5600, molecular weight distribution 1.2). The functionalization rate of the polymer (A) was calculated using ¹ H NMR (Varian's Gemini-300, measuring solvent = carbon tetrachloride / heavy acetone = 4/1 mixed solvent, quantification method = initiator residue Based on the signal (7.2 ppm), the signal of methylene adjacent to the terminal (meth) acryloyl substituent (4.00 ppm) is compared and quantified). As a result, the amount of the (meth) acryloyl substituent introduced into the obtained polymer (A) was 1.2 per molecule.

Example 1
100 parts by weight of an isobutylene polymer having a (meth) acryloyl-based substituent at the terminal as described in Synthesis Example 1 is added to a minicup, and 100 parts by weight of isobornyl acrylate (IBXA, Osaka Organic Chemical Industries, Ltd.), 2- 2.6 parts by weight of hydroxy-2-methyl-1-phenyl-propan-1-one (DAROCURE 1173 manufactured by BASF), bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide (IRGACURE 819 manufactured by BASF) 1 .3 parts by weight was added and stirred well with a spatula to obtain a curable composition.

The obtained curable composition was separately applied on a glass plate coated with a release material so as to have a thickness of 0.1 mm. These were irradiated with a UV irradiation apparatus (model: LIGHT HAMMER 6, light source: mercury lamp lamp, integrated light quantity: 3000 mJ / cm ² ) manufactured by Fusion UV System, and a film-like cured product was obtained. The film-like cured product obtained by the above operation was subjected to a moisture permeability test described in JIS Z 0208. Moreover, the presence or absence of the crack of a film by bending another film-like hardened | cured material 180 degree | times was investigated. The results are shown in Table 1.

(Example 2)
100 parts by weight of an isobutylene polymer having a (meth) acryloyl substituent at the end as described in Synthesis Example 1 is added to a minicup, and 50 parts by weight of isobornyl acrylate (IBXA manufactured by Osaka Organic Chemical Industry Co., Ltd.), acrylic acid 50 parts by weight of lauryl (Kyoeisha Chemical Industry Co., Ltd. Light Acrylate LA), 2.6 parts by weight of 2-hydroxy-2-methyl-1-phenyl-propan-1-one (DAROCURE 1173 manufactured by BASF), bis ( A curable composition was obtained by adding 1.3 parts by weight of 2,4,6-trimethylbenzoyl) -phenylphosphine oxide (IRGACURE819, manufactured by BASF) and stirring well with a spatula.
The obtained curable composition was cured by the same method as in (Example 1) to obtain a cured product and evaluated. The results are shown in Table 1.

Example 3
100 parts by weight of an isobutylene-based polymer having a (meth) acryloyl-based substituent at the terminal as described in Synthesis Example 1 is added to a minicup, and 100 parts by weight of lauryl acrylate (Light Eye LA, manufactured by Kyoeisha Chemical Co., Ltd.) 2.6 parts by weight of 2-hydroxy-2-methyl-1-phenyl-propan-1-one (DAROCURE 1173 manufactured by BASF), bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide (manufactured by BASF) IRGACURE819) 1.3 parts by weight was added and stirred well with a spatula to obtain a curable composition.
The obtained curable composition was cured by the same method as in (Example 1) to obtain a cured product and evaluated. The results are shown in Table 1.

(Comparative Example 1)
100 parts by weight of the isobutylene polymer (A) having a (meth) acryloyl substituent at the end as described in Synthesis Example 1 is added to a minicup, and 2-hydroxy-2-methyl-1-phenyl-propan-1-one (BASF DAROCURE 1173) 2.6 parts by weight and bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide (BASF IRGACURE 819) 1.3 parts by weight are added and stirred well with a spatula. Thus, a curable composition was obtained.
The obtained curable composition was cured by the same method as in Example 1 to obtain a cured product and evaluated. The results are shown in Table 1.

(Comparative Example 2)
A photocurable epoxy adhesive (XNR5516Z manufactured by Nagase ChemteX Corp.) was cured in the same manner as in Example 1 to obtain a cured product and evaluated. The results are shown in Table 1.

(Comparative Example 3)
100 parts by weight of an isobutylene polymer having a (meth) acryloyl substituent at the end as described in Synthesis Example 1 is added to a minicup, and 50 parts by weight of methyl acrylate (manufactured by Wako Pure Chemical Industries, Ltd.) is added. Stir with a spatula. These components were not compatible and phase separation occurred.

  When Example 1 and Comparative Example 1 are compared, all the cured products show excellent flexibility and moisture permeation resistance, but the curable composition of Example 1 has a low viscosity and is used when a film-like cured product is produced. Workability in coating was good.

  Further, when Example 1 and Comparative Example 2 are compared, both show the same level of moisture permeability, but Comparative Example 2 has a high viscosity and breaks when the cured film is folded. The viscosity was small and the film-like cured product was not broken.

Claims (9)

General formula (1):
—Z—C (═O) —NH—R ² —O—C (═O) —C (R ¹ ) ═CH ₂ (1)
(Wherein R ¹ is a hydrogen atom or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms, R ² is — (CH ₂ ) ₂ —, — (CH ₂ ) ₃ —, — (CH _{2) 6 -, - (CH} 2) 2 -O- (CH 2) 2 -, or, p- phenylene, Z is a heteroatom, NR ³ (R ³ is a hydrogen atom or a substituted or unsubstituted carbon A saturated hydrocarbon polymer (A) having an average of 1 or more substituents in the molecule, which is a group selected from hydrocarbon groups having 1 to 20 atoms),
(Meth) acrylic monomer (B) selected from isobornyl acrylate or lauryl acrylate,
And polymerization initiator (C),
Contain,
The saturated hydrocarbon polymer (A) is an isobutylene polymer,
The curable composition whose quantity of the said (meth) acrylic-type monomer (B) is 30 to 200 weight part with respect to 100 weight part of said saturated hydrocarbon type polymers (A) . The curable composition according to claim 1, wherein R ^{1 in the} general formula (1) is a hydrogen atom or a methyl group. The curable composition according to claim 1 or 2, wherein R ^{1 in the} general formula (1) is a hydrogen atom. The curable composition according to any one of claims 1 to 3 , wherein the substituent represented by the general formula (1) has only a terminal of the saturated hydrocarbon polymer (A). Wherein the polymerization initiator (C) is a photoradical initiator that generates radicals by light, curable composition according to any one of claims 1-4. 50 to 200 parts by weight of the (meth) acrylic monomer (B) and 0.001 to 10 parts by weight of the polymerization initiator (C) are included with respect to 100 parts by weight of the saturated hydrocarbon polymer (A). The curable composition according to any one of claims 1 to 5 . The saturated hydrocarbon polymer (A) having the same main chain skeleton as the saturated hydrocarbon polymer (A) and having a hydroxyl group at the terminal, and the general formula (4) :
^{O = C = N-R 2} -O-C (= O) -C (R 1) = CH 2 (4)
(Wherein R ¹ is a hydrogen atom or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms, R ² is — (CH ₂ ) ₂ —, — (CH ₂ ) ₃ —, — (CH ₂ ) _6- , — (CH ₂ ) ₂ —O— (CH ₂ ) ₂ —, or p-phenylene )), obtained by reacting with an isocyanate compound (D). The curable composition according to any one of claims 1 to 6 . The curable composition according to claim 7 , wherein the curable composition is obtained by reacting a saturated hydrocarbon polymer (a) with an isocyanate compound (D) using an organotin compound (E) as a catalyst. Hardened | cured material obtained by hardening the curable composition of any one of Claim 1 to 8 .