TW201418344A - Curing agent and resin composition using same - Google Patents

Abstract

The present invention provides: a curing agent for an epoxy resin and/or resin having at least one unsaturated bond in the molecule, the curing agent comprising a compound having at least one primary amino group in the molecule, and the compound being obtained by reacting an isocyanate compound and hydrazine or a polyvalent amine compound having two or more primary amino groups in the molecule; a resin composition and liquid crystal sealant composition using the same; a liquid crystal display panel; and a method for producing a liquid crystal display panel.

Description

Hardener and resin composition using the same

The present invention relates to a hardener for a resin having at least one unsaturated bond in an epoxy resin and/or a molecule, and particularly relates to a hardener which can be applied to a liquid crystal display element such as a liquid crystal display, a resin composition using the same, A liquid crystal sealant composition, a liquid crystal display panel, and a method of manufacturing the same.

In recent years, with the expansion of the display portion of the liquid crystal display and the narrow frame, the sealant has been thinned. In addition, as a sealing agent, not only glass, an inorganic material such as an ITO electrode or a SiN film, an organic material such as an alignment film, but also an organic material such as an alignment film may be attached, and the adherend may be diversified, and the sealant may pursue a dissimilar material. Then the diversity of sex.

As a sealing agent for the dissimilar materials, for example, a curing agent such as a curable resin such as an epoxy group (meth)acrylate or a curing agent such as a thermal epoxy curing agent, and a liquid crystal display element containing no inorganic filler are proposed. Sealant (Patent Document 1). In the case of the thermal epoxy curing agent used for the sealing agent for liquid crystal display elements, such as diterpene sebacate, diterpene diisophthalate, diammonium adipate, etc., as other commercially available products. , For example, AJICUREVDH, AJICUREUDH (all manufactured by Ajinomoto Fine-Techno Co., Inc.), and the like can be mentioned.

[Previous Technical Literature] [Patent Literature]

[Patent Document 1] Japanese Patent Laid-Open Publication No. 2010-85712

In order to suppress the peeling of the cell and the peeling of the IC for driving the liquid crystal cell during the mounting of the sealing agent, the sealing agent is also required to further improve the bonding strength.

SUMMARY OF THE INVENTION An object of the present invention is to provide a curing agent which satisfies the requirements of the thinning and adhesion of a sealant, and at the same time, provides a latent strength enhancing epoxy resin and/or has at least one unsaturated bond in the molecule. A hardener for a resin, a resin composition using the same, and a liquid crystal sealant composition.

In order to solve the above problems, the inventors of the present invention have made an effort to review and find that a compound having a urea structure in the molecule and having at least one first-order amine group is used as an epoxy resin and/or has at least one unsaturated in the molecule. A latent hardening agent for a bonded resin, which can obtain a thinning and adhesion of a sealant such as a liquid crystal display panel, and can be connected A resin composition having a high strength and a liquid crystal sealant composition.

That is, the present invention is as described in [1] to [14].

[1] An epoxy containing a compound having at least one first-order amine group in a molecule obtained by a reaction of an isocyanate compound, a hydrazine or a polyvalent amine compound having two or more first-stage amine groups in the molecule. A resin and/or a hardener for a resin having at least one unsaturated bond in the molecule.

[2] contains the following formula (I)

[in the formula

R ² is a single bond, or a C ₁ -C ₁₂ alkyl group, a C ₂ -C ₁₂ alkyl group interrupted discontinuously by one or more NH (imine groups) or O atoms (oxygen atoms) (H atom (hydrogen atom) bonded to N atom (nitrogen atom) may be substituted by an amine group or a C ₁ -C ₁₂ alkylamine group), C ₃ -C ₁₂ cycloalkyl group, C ₁ ~ C ₁₂ alkylene-C ₃ ~C ₁₂ cycloalkyl, C ₁ ~C ₁₂ alkyl -C ₃ ~C ₁₂ cycloalkyl-C ₁ ~C ₁₂ alkyl, C ₃ ~ C ₁₂ ring Alkyl-C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl, C ₆ -C ₁₄ aryl, C ₁ -C ₄ alkyl -C ₆ -C ₁₄ aryl, C ₁ -C ₄ alkylene-C ₆ -C ₁₄ extended aryl-C ₁ -C ₄ alkylene group, or C ₆ -C ₁₄ extended aryl group -C ₁ -C ₄ alkylene group -C ₆ -C ₁₄ Extending an aryl group (here, an alkyl group is a straight or branched chain and may be substituted by halogen, a C ₃ -C ₁₂ cycloalkyl group or a C ₆ -C ₁₄ extended aryl group is unsubstituted, or is halogen or C ₁ -C ₄ alkyl group substituted), n is 1, 2, 3 or 4, and when n is 2 or more, R ^{1 is} independent, and when n is 1, A is a C ₁ -C ₁₂ alkyl group. C ₂ -C ₁₂ alkyl group, C ₂ -C ₁₂ alkyloxycarbonyl group discontinuously interrupted by one or more O atoms (oxygen atoms) Alkyl, C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl, C ₃ -C ₁₂ cycloalkyl-C ₁ -C ₁₂ alkyl-C ₃ ~ C ₁₂ cycloalkyl, C ₆ ~ C ₁₄ aryl, C ₁ ~ C ₄ alkyl - C ₆ ~ C ₁₄ extended aryl, C ₆ ~ C ₁₄ aryl - C ₁ ~ C ₄ alkyl -C ₆ ~C ₁₄ extended aryl (here, the alkyl group is a straight or branched chain and can be substituted by halogen, C ₃ ~ C ₁₂ cycloalkyl, C ₃ ~ C ₁₂ cycloalkyl, C ₆ ~ C Where ₁₄ aryl, or C ₆ -C ₁₄ aryl is unsubstituted, or substituted by halogen or C ₁ -C ₄ alkyl), or (meth) acryloxyalkyl, n is 2 A is a C ₁ -C ₁₂ alkyl group, a C ₂ -C ₁₂ alkyl group interrupted by one or more O atoms (oxygen atoms), and a C ₁ -C ₁₂ alkyloxycarbonyl group. Alkyl, C ₃ ~C ₁₂ cycloalkyl, C ₁ ~C ₁₂ alkyl -C ₃ ~C ₁₂ cycloalkyl, C ₁ ~C ₁₂ alkyl -C ₃ ~C ₁₂ cyclohexane -C ₁ -C ₁₂ alkyl, C ₃ -C ₁₂ cycloalkyl-C ₁ -C ₁₂ alkyl -C ₃ -C ₁₂ cycloalkyl, di C ₃ -C ₁₂ cycloalkanediyl , C ₆ ~ C ₁₄ arylene group, C ₁ ~ C ₄ alkylene -C ₆ ~ C ₁₄ arylene group -C ₁ ~ C ₄ alkylene, or C ₆ ~ C ₁₄ arylene group -C ₁ ~ C ₄ alkylene-C ₆ ~C ₁₄ extended aryl (here, the alkyl group is a straight or branched chain and may be substituted by halogen, C ₃ ~ C ₁₂ cycloalkyl, C ₆ ~ C ₁₄ extended aryl is unsubstituted, or halogen or When C ₁ -C ₄ alkyl is substituted), when n is 3, A is the following formula (1)

(wherein R ^{2 is the} same or different and is a C ₁ to C ₁₂ alkyl group of a straight or branched chain), and the following formula (2)

(wherein R ^{3 is the} same or different and is a C ₁ to C ₁₂ alkyl group of a straight or branched chain) or the following formula (3)

(Wherein, R ⁴ are the same or different, is a straight-chain or branched-chain C ₁ ~ C ₁₂ alkylene, R ⁵ is CH), n is 4 where, A is the following formula (4)

Wherein X ³ is Si, or C ₃ -C ₁₂ cycloalkyl-C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl, or C ₆ -C ₁₄ aryl-C ₁ -C _4- alkyl-C ₆ -C ₁₄ aryl (here, the alkyl group is a straight or branched chain, which may be substituted by 1 to 6 halogens, C ₃ to C ₁₂ cycloalkyl or C ₆ to C ₁₄ An epoxy resin having a compound having at least one first-order amine group in a molecule represented by a tetravalent residue derived from a tetravalent residue derived from a halogen or a C ₁ -C ₄ alkyl group; / or a hardener for a resin having at least one unsaturated bond in the molecule.

[3] A compound having at least one first-order amine group in the molecule is represented by the following formula (Ia)

Wherein R ^{1 is} independently the same as the above [2], and X ¹ is a C ₁ to C ₁₂ alkyl group, and C ₂ to C are discontinuously interrupted by one or more O atoms (oxygen atoms). ₁₂ alkyl, C ₁ ~ C ₁₂ alkyloxycarbonyl alkyl, C ₃ ~ C ₁₂ cycloalkyl, C ₁ ~ C ₁₂ alkyl - C ₃ ~ C ₁₂ cycloalkyl, C ₁ ~ C ₁₂ alkyl-C ₃ ~ C ₁₂ cycloalkyl-C ₁ ~ C ₁₂ alkyl, C ₃ ~ C ₁₂ cycloalkyl - C ₁ ~ C ₁₂ alkyl - C ₃ ~ C ₁₂ cycloalkylene, di C ₃ ~C ₁₂ cycloalkane diyl, C ₆ ~C ₁₄ extended aryl, C ₁ ~C ₄ alkyl -C ₆ ~C ₁₄ extended aryl-C ₁ ~C ₄ Alkyl, or C ₆ -C ₁₄ aryl-C ₁ -C ₄ alkyl-C ₆ -C ₁₄ extended aryl (here, alkyl is straight or branched and can be substituted by halogen, C ₃ ~ C ₁₂ cycloalkyl alkylene or C ₆ ~ C ₁₄ arylene group is unsubstituted, by halogen or C ₁ ~ C ₄ alkyl group substituted with the above-described [2] according to the hardener)] in.

[4] A compound having at least one first-order amine group in the molecule is represented by the following formula (IIa)

[Wherein, R ¹ is synonymous with the above-described [2], X ² is C ₁ ~ C ₁₂ alkyl group, at least one O atom or a (an oxygen atom) discontinuous interrupted C ₂ ~ C ₁₂ alkyl group , C ₁ -C ₁₂ alkyloxycarbonylalkylene, C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl, C ₃ -C ₁₂ cycloalkyl -C ₁ ~C ₁₂ alkylene-C ₃ ~C ₁₂ cycloalkyl, C ₆ -C ₁₄ aryl, C ₁ -C ₄ alkyl-C ₆ ~C ₁₄ extended aryl, C ₆ ~C ₁₄ Aryl-C ₁ -C ₄ alkylene-C ₆ -C ₁₄ extended aryl (here, the alkyl group is a straight or branched chain and can be substituted by halogen, C ₃ -C ₁₂ cycloalkyl, C ₃ ~ C ₁₂ cycloalkylene, C ₆ -C ₁₄ aryl or C ₆ -C ₁₄ extended aryl is unsubstituted or substituted by halogen or C ₁ -C ₄ alkyl), or (meth)acryl fluorenyl The oxyalkyl group described in the above [2].

[5] Further containing a compound obtained by treating a compound having at least one first-stage amine group in the molecule with an isocyanate compound The curing agent according to any one of the above [1] to [4].

[6] A hardener according to any one of the above [1] to [4], which further comprises a compound obtained by treating a compound having at least one first-order amine group in the molecule with an isocyanate compound and an epoxy resin; .

[7] The curing agent according to any one of the above [1] to [4], which further comprises a compound obtained by treating a compound having at least one first-stage amine group in the molecule with an isocyanate compound and a compound having a hydroxyl group.

[8] A resin composition comprising the curing agent (A) according to any one of the above [1] to [7], an epoxy resin, and/or a resin (B) having at least one unsaturated bond.

[9] The epoxy resin is a resin composition according to the above [8], which is a partially esterified epoxy resin obtained by reacting 1 equivalent of an epoxy group with an epoxy group of 10 to 90 equivalent % of (meth)acrylic acid.

[10] The resin composition according to the above [8] or [9], wherein the total amount of the first-stage amine groups contained in the curing agent (A) is 0.001 to 10 equivalents per equivalent of the epoxy group.

[11] A total of 1 equivalent of the epoxy group of the epoxy resin and 1 equivalent of the unsaturated bond of the resin having at least one unsaturated bond in the molecule, and the first-stage amine group contained in the hardener (A) The resin composition of any one of the above [8] to [10] is 0.001 to 10 equivalents.

[12] The method according to any one of the above [8] to [11] A liquid crystal sealant composition of a resin composition.

[13] A liquid crystal display panel obtained by using the liquid crystal sealing agent composition according to the above [12].

[14] A method of producing a liquid crystal display panel which is subjected to photocuring and then thermally cured by using the liquid crystal sealing agent composition according to the above [12].

According to the present invention, it has been found that it is possible to adapt to the thinning of the sealing agent such as a liquid crystal display panel and the versatility of the adhesiveness, and at the same time, it is possible to exhibit the peeling of the IC during the cutting out of the cell and the mounting of the IC for driving the liquid crystal cell. The strength of the next.

1‧‧‧ glass substrate

2‧‧‧Liquid sealant composition

3‧‧‧LCD injection hole

4‧‧‧ glass substrate

5‧‧‧Liquid cell for liquid crystal encapsulation

6‧‧‧LCD

7‧‧‧LCD panel

8‧‧‧ITO glass

9‧‧‧ glass

10‧‧‧Test strips

Fig. 1 is an explanatory view showing an embodiment of a liquid crystal display panel produced by using a liquid crystal sealant composition.

Fig. 2 is an explanatory view for explaining a test method of the adhesion strength of the liquid crystal sealant composition.

The numerical range expressed by "~" in the present specification is a range including the minimum value and the maximum value of the numerical values described before and after "~". When the amount of each component in the composition is plural in the composition corresponding to each component, it is not particularly limited, and refers to the total amount of the plural substances present in the composition. The description of "C _a ~ C _b " refers to the range of carbon numbers a to b.

[hardener]

The present invention is an epoxy containing a compound having at least one first-order amine group in a molecule obtained by a reaction of an isocyanate compound, a hydrazine or a polyvalent amine compound having two or more amine groups in the molecule. A resin and/or a hardener for a resin having at least one unsaturated bond in the molecule. By using a hardener containing a compound having a urea structure in addition to at least one first-stage amine group in the molecule, as an epoxy resin and/or a resin having at least one unsaturated bond in the molecule (for example, (meth) In addition to being suitable for the thinning of the sealing agent such as a liquid crystal display panel and the versatility of the sealing agent, the latent curing agent can suppress the IC at the time of cutting out of the cell and the IC for driving the liquid crystal cell. The strength of the peeling of the peeling during mounting.

By an isocyanate compound, with a hydrazine or intramolecular 2 Since the compound obtained by the reaction of the polyvalent amine compound of the first-stage amine group has a urea structure and at least one first-order amine group in the molecule, it is presumed that the hydrogen bonding force with the adherend is improved and becomes higher than The hydrazine compound or the amine compound used as the hardener is then stronger.

[isocyanate compound]

The isocyanate compound used in the present invention is a compound having at least one isocyanate group (-N=C=O), and is not particularly limited, but may be exemplified. For example, a monoisocyanate compound, a diisocyanate compound, a triisocyanate compound, a tetraisocyanate compound, or the like.

(monoisocyanate compound)

The monoisocyanate compound is, for example, a compound represented by the following formula (1a).

In the formula (1a), X ² is a C ₁ -C ₁₂ alkyl group, and C ₂ -C ₁₂ alkyl group or C ₁ -C ₁₂ alkyl group which is discontinuously interrupted by one or more O atoms (oxygen atoms). Oxycarbonylcarbonylalkyl, C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl, C ₃ -C ₁₂ cycloalkyl-C ₁ -C ₁₂ alkylene -C ₃ -C ₁₂ cycloalkyl, C ₆ -C ₁₄ aryl, C ₁ -C ₄ alkyl-C ₆ -C ₁₄ extended aryl, C ₆ -C ₁₄ aryl-C ₁ ~C ₄ Alkyl-C ₆ -C ₁₄ extended aryl (here, the alkyl group is a straight or branched chain and can be substituted by halogen, C ₃ -C ₁₂ cycloalkyl, C ₃ -C ₁₂ cycloalkyl, C ₆ ~ C ₁₄ aryl, or C ₆ ~ C ₁₄ extended aryl is unsubstituted, or substituted by halogen or C ₁ ~ C ₄ alkyl), or (meth) acryl decyl oxyalkyl. X ² in the formula (1a) is synonymous with A in the case where n is 1 in the formula (I).

In the present specification, in combination with other terms, "C ₁ -C ₁₂ alkyl group" is a straight chain or a branched chain, and may be substituted by halogen, and may be one or more O atoms (oxygen atoms). Non-continuous interruption, preferably linear. Range of carbon atoms is an alkyl group of C ₁ ~ C _12, more preferably C ₁ ~ C _8, then good is C ₁ ~ C _6, and particularly preferably the range of C ₁ ~ C _4. Specific examples thereof include, for example, methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, n-fluorenyl, n-fluorenyl Linear chain of n-undecyl, n-dodeyl, etc., isopropyl, isobutyl, sec-butyl, t-butyl, 2-methylbutyl, isooctyl, t-octyl A branch of a group such as a 2-ethylhexyl group or a t-fluorenyl group. Examples of the halogen include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. The halogen as a substituent is preferably a fluorine atom or a chlorine atom, more preferably a fluorine atom. The number of substitutions is 1 to 12, preferably 1 to 6, more preferably 1 to 4, and particularly preferably 1 to 3.

In the present specification, in combination with other terms, "C ₁ -C ₁₂ alkyl" is a straight or branched chain, which may be substituted by halogen, and may be substituted by one or more NH (imine groups). Or the O atom (oxygen atom) is discontinuously discontinuous (the H atom (hydrogen atom) bonded to the N atom (nitrogen atom) may be substituted by an amine group or a C ₁ -C ₁₂ alkylamine group), Good for the chain. Range of carbon atoms of the alkylene group of C ₁ ~ C _12, more preferably C ₁ ~ C _8, then good is C ₁ ~ C _6, and particularly preferably the range of C ₁ ~ C _4. Specific examples thereof include, for example, methylene, ethyl, trimethylene, propyl, tetramethylene, 1-methyltrimethylene, 2-methyltrimethylene, 3-methyltrimethylene , pentamethylene, 1-methyltetramethylene, 4-methyltetramethylene, hexamethylene, 5-methylpentamethylene, heptamethylene, octamethyl, Kyua Methyl, decamethylene, undecylmethyl, dodecamethylene and the like. Examples of the halogen include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. The halogen as a substituent is preferably a fluorine atom or a chlorine atom, more preferably a fluorine atom. The number of substitutions is 1 to 12, preferably 1 to 6, more preferably 1 to 4, and particularly preferably 1 to 3.

In the present specification, the carbon number of the alkyloxy group or the alkyloxy group of "C ₁ -C ₁₂ alkyloxycarbonylalkylene group" or "C ₁ -C ₁₂ alkylalkyloxycarbonylalkylene group" The range is from C ₁ to C ₁₂ , more preferably from C ₁ to C ₈ , still more preferably from C ₁ to C ₆ , and particularly preferably from C ₁ to C ₄ . Specific examples thereof include, for example, methoxycarbonylmethylene, ethoxycarbonylmethylene, n-propoxycarbonylmethylene, n-butoxycarbonylmethylene, n-pentyloxycarbonyl , n-hexyloxycarbonylmethylene, n-heptyloxycarbonylmethylene, n-octyloxycarbonylmethylene, n-fluorenyloxycarbonylmethylene, n-decyloxy Linear chain such as carbonylcarbonylmethylene, n-undecyloxycarbonylmethylene, n-dodecyloxycarbonylmethylene, etc., isopropoxycarbonylmethylene, isobutoxycarbonyl Methyl, sec-butoxycarbonylmethylene, t-butoxycarbonylmethylene, 2-methylbutoxycarbonylmethylene, isooctyloxycarbonylmethylene, t-octyloxy A branch of a carbonylcarbonylmethylene group, a 2-ethylhexyloxycarbonylmethylene group or the like.

In the present specification, the carbon number of "C ₃ -C ₁₂ cycloalkyl group" alone or in combination with other terms is in the range of C ₃ to C ₁₂ , more preferably C ₃ to C ₈ , and even more preferably C _{3 .} ~ C _6, and particularly preferably the range of C ₄ ~ C _6. Specific examples thereof include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, a cyclodecyl group, a cyclodecyl group, a cyclodecyl group, and a cyclododecyl group. C ₃ -C ₁₂ cycloalkyl, preferably cyclopentyl or cyclohexyl. The C ₃ -C ₁₂ cycloalkyl group is unsubstituted or may be substituted by a halogen or a C ₁ -C ₄ alkyl group, and examples of the halogen include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. The halogen as a substituent is preferably a fluorine atom or a chlorine atom, more preferably a chlorine atom. Examples of the C ₁ to C ₄ alkyl group as a substituent include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a t-butyl group. The C ₁ -C ₄ alkyl group as a substituent is preferably a methyl group, an ethyl group or an n-propyl group, more preferably a methyl group or an ethyl group. The number of substitutions in the case of having a substituent is 1 to 5, preferably 1 to 3, more preferably 1 to 2, and particularly preferably 1.

In the present specification, the carbon number of "C ₃ -C ₁₂ cycloalkylene group" alone or in combination with other terms is in the range of C ₃ to C ₁₂ , more preferably C ₃ to C ₈ , and even more preferably C. ₃ ~ C ₆ , especially preferably in the range of C ₄ ~ C ₆ . Specific examples thereof include, for example, a cyclic propyl group, a cyclo-butyl group, a cyclopentyl group, a cyclohexyl group, a cyclo-heptyl group, a cyclo-extension group, a ring-extension group, a ring-extension group, and a ring extension. One base and the ring extend twelve bases. The C ₃ -C ₁₂ cycloalkyl group is preferably a cyclopentyl group or a cyclohexyl group. The C ₃ -C ₁₂ cycloalkyl group is unsubstituted or may be substituted by halogen or C ₁ -C ₄ alkyl, and examples of the halogen include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom. The halogen as a substituent is preferably a fluorine atom or a chlorine atom, more preferably a chlorine atom. Examples of the C ₁ to C ₄ alkyl group as a substituent include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a t-butyl group. The C ₁ -C ₄ alkyl group as a substituent is preferably a methyl group, an ethyl group or an n-propyl group, more preferably a methyl group or an ethyl group. The number of substitutions in the case of having a substituent is 1 to 4, preferably 1 to 3, more preferably 1 to 2, and particularly preferably 1.

In the present specification, the "C ₆ -C ₁₄ aryl group" is a monovalent group having at least one aromatic ring, alone or in combination with other terms. Specific examples thereof include a phenyl group, a biphenyl group, a naphthyl group, an anthracenyl group, and a phenanthrene group. It is preferably a phenyl group, a biphenyl group or a naphthyl group, more preferably a phenyl group or a naphthyl group. The C ₆ -C ₁₄ aryl group is unsubstituted or may be substituted by halogen or a C ₁ -C ₄ alkyl group, and examples of the halogen include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom. The halogen as a substituent is preferably a fluorine atom or a chlorine atom, more preferably a chlorine atom. Examples of the C ₁ to C ₄ alkyl group as a substituent include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a t-butyl group. The C ₁ -C ₄ alkyl group as a substituent is preferably a methyl group, an ethyl group or an n-propyl group, more preferably a methyl group or an ethyl group. The number of substitutions in the case of having a substituent is 1 to 5, preferably 1 to 3, more preferably 1 to 2, and particularly preferably 1.

In the present specification, the "C ₆ -C ₁₄ exoaryl group" is a divalent group having at least one aromatic ring, either alone or in combination with other terms. Specific examples thereof include a stretching phenyl group, a stretching naphthyl group, a stretching group, and a phenanthrene group. It is preferably a phenyl group or a naphthyl group, more preferably a phenyl group or a naphthyl group. The C ₆ -C ₁₄ extended aryl group is unsubstituted or may be substituted by halogen or a C ₁ -C ₄ alkyl group, and examples of the halogen include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom. The halogen as a substituent is preferably a fluorine atom, a chlorine atom or a bromine atom, more preferably a fluorine atom or a chlorine atom. Examples of the C ₁ to C ₄ alkyl group as a substituent include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a t-butyl group. The C ₁ -C ₄ alkyl group as a substituent is preferably a methyl group, an ethyl group or an n-propyl group, more preferably a methyl group or an ethyl group. The number of substitutions in the case of having a substituent is 1 to 4, preferably 1 to 3, more preferably 1 to 2, and particularly preferably 1.

(meth)acrylonitrile group as a monoisocyanate compound The oxyalkyl isocyanate may, for example, be a compound represented by the following formula (1b).

In the formula (1b), R ⁶ is a hydrogen atom or a methyl group, and R ⁷ is a C ₁ -C ₆ alkylene group. The range of the carbon number of the C ₁ to C ₆ alkyl group of R ⁷ is preferably C ₂ to C ₆ , more preferably C ₃ to C ₆ .

Specific examples of the monoisocyanate compound include methyl isocyanate, ethyl isocyanate, n-hexyl isocyanate, cyclohexyl isocyanate, 2-ethylhexyl isocyanate, phenyl isocyanate, benzyl isocyanate, propyl isocyanate, and isopropyl isocyanate. , butyl isocyanate, heptyl isocyanate, dodecyl isocyanate, octadecyl isocyanate, t-butyl isocyanate, ethyl isocyanatoacetate, butyl isocyanatoacetate, (S)-(-)-2 -methyl isocyanatopropionate, 1-naphthyl isocyanate, 4-chlorophenyl isocyanate, 4-fluorophenyl isocyanate, phenyl ethyl isocyanate, p-cresyl isocyanate , m-cresyl isocyanate, 3,5-dimethylphenyl isocyanate, and the like.

Specific examples of the (meth) propylene decyloxyalkyl isocyanate include (meth) propylene decyloxymethyl isocyanate, (meth) propylene decyl oxyethyl isocyanate, and (meth) propylene oxime. Alkoxypropyl isocyanate or the like.

(diisocyanate compound)

The diisocyanate compound is, for example, a compound represented by the following formula (2a).

In the formula (2a), X ¹ is a C ₁ to C ₁₂ alkyl group, and C ₂ to C ₁₂ alkyl groups which are discontinuously interrupted by one or more O atoms (oxygen atoms), C ₁ to C ₁₂ Alkyloxycarbonylalkylene, C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl -C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl -C ₃ ~C ₁₂ cycloalkyl-C ₁ ~C ₁₂ alkyl, C ₃ ~C ₁₂ cycloalkyl-C ₁ ~C ₁₂ alkyl -C ₃ ~C ₁₂ cycloalkyl, two C ₃ ~ C ₁₂ cycloalkane diyl, C ₆ -C ₁₄ aryl, C ₁ -C ₄ alkyl -C ₆ -C ₁₄ aryl-C ₁ -C ₄ alkyl, or C ₆ -C ₁₄ Aryl-C ₁ -C ₄ alkylene-C ₆ -C ₁₄ extended aryl (here, the alkyl group is a straight or branched chain and can be substituted by halogen, C ₃ -C ₁₂ cycloalkyl or C ₆ The ~C ₁₄ extended aryl group is unsubstituted or substituted by halogen or C ₁ -C ₄ alkyl). X ¹ in the formula (2a) is synonymous with A in the case where n is 2 in the formula (I).

Specific examples of the diisocyanate compound include diphenyl Methane diisocyanate (MDI), methylphenyl diisocyanate (TDI), xylene diisocyanate (XDI), hydrogenated xylene diisocyanate (hydrogenated XDI), isophorone diisocyanate (IPDI), toluidine II Isocyanate (TPDI), hexamethylene diisocyanate (HDI), dicyclohexylmethane diisocyanate (HMDI), 2,4,4-trimethylhexamethylene diisocyanate (TMHDI), 3,5,5- Trimethylhexamethylene diisocyanate (TMHDI), 4,4'-diisocyanooxy-3,3'-dimethylbiphenyl ester, 4,4'-diisocyanooxy-3,3 '-Dimethyldiphenylmethane, 2,2-bis(4-isocyanatophenyl)hexafluoropropane, 2,4-diisocyanoxytoluene, 1,3-bis(2-isocyanide) Oxy-2-propyl)benzene, methylphenyl-2,6-diisocyanate, 1,4-phenylene diisocyanate, 1,3-phenylene diisocyanate, 1,5-diiso Cyanooxynaphthalene and the like.

(triisocyanate compound)

The triisocyanate compound may, for example, be an isocyanurate structure having an isocyanate group at the three ends, or a compound having a biuret structure or an adduct structure. The triisocyanate compound having an isocyanurate structure may, for example, be a compound having an isocyanurate structure represented by the following formula (3a).

Wherein R ^{2 is the} same or different and is a linear or branched C ₁ -C ₁₂ alkyl group.

The triisocyanate compound having a biuret structure may, for example, be a compound represented by the following formula (3b).

Wherein R ^{3 is the} same or different and is a linear or branched C ₁ -C ₁₂ alkyl group.

The triisocyanate compound having an adduct structure is, for example, a compound represented by the following formula (3c).

Wherein R ^{4 is the} same or different and is a linear or branched C ₁ -C ₁₂ alkyl group, and R ⁵ is CH.

Specific examples of the triisocyanate compound include tris(isocyanatomethyl)isocyanurate, tris(isocyanatoethyl)isocyanurate, and tris(isocyanatopropyl)isocyanate. Urea, tris(isocyanooxybutyl)isocyanurate, tris(isocyanatohexyl)isocyanurate, N,N'-2-tris-isocyanate methylmalonate , N, N'-2-tris-isocyanate hexyl malonate and the like.

(tetraisocyanate compound)

The tetraisocyanate compound is, for example, a compound represented by the following formula (4a).

Wherein X ³ is C ₃ -C ₁₂ cycloalkyl-C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl or C ₆ -C ₁₄ aryl-C ₁ -C ₄ alkyl -C ₆ -C ₁₄ aryl (alkyl group is straight or branched and may be substituted by halogen, C ₃ -C ₁₂ cycloalkyl or C ₆ -C ₁₄ aryl is unsubstituted, or halogen or C ₁ ~ The C ₄ alkyl group may also be substituted with a tetravalent group derived.

Further, the tetraisocyanate compound may, for example, be tetraisocyanooxydecane represented by the following formula (4b).

Specific examples of the tetraisocyanate compound include 4,4'-diphenylmethane-2,2',5,5'-tetraisocyanate and tetraisocyanooxydecane.

[polyvalent amine compound]

The polyvalent amine compound is a compound having at least two first-order amine groups, and examples thereof include a polyvalent amine compound represented by the following formula (5a).

[Chemical 16] NH ₂ -L-NH ₂ . . . (5a)

In the formula, L is a C ₁ -C ₁₂ alkyl group, and a C ₂ -C ₁₂ alkyl group (bond) which is discontinuously interrupted by one or more NH (imine groups) or O atoms (oxygen atoms) H atom (hydrogen atoms) in N junction atom (a nitrogen atom) is substituted by amino or C ₁ ~ C ₁₂ alkyl group can), C ₃ ~ C ₁₂ cycloalkyl alkylene, C ₁ ~ C ₁₂ extending Alkyl-C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl-C ₁ -C ₁₂ alkyl, C ₃ -C ₁₂ cycloalkyl -C ₁ ~C ₄ alkylene-C ₃ ~C ₁₂ cycloalkyl, C ₆ ~C ₁₄ extended aryl, C ₁ ~C ₄ alkyl -C ₆ ~C ₁₄ extended aryl, C ₁ ~ C ₄ alkylene-C ₆ ~C ₁₄ extended aryl-C ₁ ~C ₄ alkylene, or C ₆ ~C ₁₄ extended aryl-C ₁ ~C ₄ alkyl -C ₆ ~C ₁₄ a base (here, an alkyl group is a straight or branched chain and may be substituted by halogen, a C ₃ -C ₁₂ cycloalkyl group or a C ₆ -C ₁₄ extended aryl group is unsubstituted, or is halogen or C ₁ -C ₄ Alkylation can also be substituted.). L in the formula (5a) is synonymous with R ¹ in the formula (I), the formula (Ia) and the formula (IIa).

The polyvalent amine compound may have, for example, two firsts. a diamine compound of the amino group, a triamine compound having three amine groups of the first order, and the like. The diamine compound having two first-order amine groups is not particularly limited, and examples thereof include aliphatic diamines, alicyclic diamines, and aromatic diamines. Further, among the compounds represented by the above formula (5a), the compound in which L is a single bond is a hydrazine.

Among the aliphatic diamines, examples of the compound having a C ₁ to C ₁₂ alkylene group include ethylene diamine, propylene diamine, 1,2-diaminopropane, and tetramethylene diamine. Pentamethylenediamine, hexamethylenediamine, heptamethylenediamine, octamethylenediamine, dodecamethylenediamine, propane-1,2-diamine, 1,2-di Amino-2-methylpropane, and the like.

Among the aliphatic diamines, specific examples of the C ₂ to C ₁₂ alkylene group having a linear or branched chain which is discontinuously interrupted by one or more O atoms (oxygen atoms) may, for example, be 2 , 2'-oxybis(ethylamine), 1,2-bis(2-aminoethoxy)ethane, 1,11-diamino-3,6,9-trioxadecane , bis(3-aminopropyl)ether, 1,4-butanediol bis(3-aminopropyl)ether, diethylene glycol bis(3-aminopropyl)ether, ethylene glycol bis ( 3-aminopropyl)ether and the like.

Among the aliphatic diamines, a C ₂ -C ₁₂ alkylene group having a linear or branched chain discontinuously interrupted by one or more NH (imine groups) (bonded to an N atom (nitrogen) The compound in which the H atom (hydrogen atom) of the atom is substituted by an amine group or a C ₁ -C ₁₂ alkylamine group may, for example, be a diethylidene triamine, a trisoleethyltetramine or a tetra. Ethyl pentamine, pentaethylidene hexamine, tris(2-aminoethyl)amine, N,N'-bis(3-aminopropyl)ethylenediamine, bis(hexamethylene) three Amine, 3,3'-diamino-N-methyldipropylamine, 3,3'-diaminodipropylamine, bis(3-aminopropyl)methylamine, and the like.

Specific examples of the alicyclic diamine include isophorone II Amine, 1,4-diaminocyclohexane, 1,3-diaminocyclohexane, trans-1,2-diaminocyclohexane, 1,3-bis(aminomethyl)cyclohexane Alkane, 4,4'-methylenebis(cyclohexylamine), and the like.

Specific examples of the aromatic diamine include p-phenylene Amine, m-phenylenediamine, p-nonanediamine, m-nonanediamine, 4,4'-diaminodiphenylmethane, 1,5-diaminonaphthalene, 1,8-diamine Ketone, 2,6-diaminotoluene, and the like.

a triamine compound having three first-order amine groups, Examples of the compound include tris(4-aminophenyl)amine, tris(3-aminopropyl)amine, and tris(2-aminoethyl)amine represented by the following formula.

Isocyanate compound with hydrazine or polyvalent amine compound For the isocyanate compound 1 mole, the hydrazine or polyvalent amine compound is preferably from 0.01 mol to 50 mol, more preferably from 0.1 mol to 50 mol, and even more preferably from 0.1 mol to 30 mol. In the range of 0.1 mol to 20 mol, in an organic solvent or neat (no solvent), preferably -10 ° C to 120 ° C, more preferably -5 ° C to 100 ° C, and more preferably 0 ° C to 50 ° C It is especially good to control the side at 5~30 °C to make it better.

Further, the curing agent contains an isocyanate group 1 mol containing an isocyanate compound and a hydrazine or a polyvalent amine compound, and the total amount of the first-stage amine group contained in the hydrazine or polyvalent amine compound is preferably. A compound which is preferably 0.01 mol to 50 mol, more preferably 0.1 mol to 50 mol, more preferably 0.1 mol to 30 mol, and particularly preferably 0.5 mol to 20 mol. .

〔hardener〕

The present invention is an epoxy resin containing a compound represented by the following formula (I) and/or a curing agent for a resin containing at least one unsaturated bond.

The hardener of the present invention contains the following formula (I)

[in the formula

R ¹ is a single bond, or a C ₁ -C ₁₂ alkyl group, one or more NH (imine groups) or an O oxygen atom (oxygen atom) discontinuously interrupted C ₂ -C ₁₂ alkyl group ( The H atom (hydrogen atom) bonded to the N atom (nitrogen atom) may be substituted by an amine group or a C ₁ -C ₁₂ alkylamine group), C ₃ to C ₁₂ cycloalkyl group, C ₁ to C ₁₂ alkyl-C ₃ ~ C ₁₂ cycloalkyl, C ₁ ~ C ₁₂ alkyl - C ₃ ~ C ₁₂ cycloalkyl - C ₁ ~ C ₁₂ alkyl, C ₃ ~ C ₁₂ ring extension Alkyl-C ₁ -C ₁₂ alkylene-C ₃ ~C ₁₂ cycloalkylene, C ₆ -C ₁₄ aryl, C ₁ -C ₄ alkyl -C ₆ -C ₁₄ extended aryl, C ₁ ~ C ₄ alkylene-C ₆ ~ C ₁₄ extended aryl - C ₁ ~ C ₄ alkyl, or C ₆ ~ C ₁₄ extended aryl - C ₁ ~ C ₄ alkyl - C ₆ ~ C ₁₄ An aryl group (here, an alkyl group is a straight or branched chain and may be substituted by halogen, a C ₃ -C ₁₂ cycloalkyl group or a C ₆ -C ₁₄ extended aryl group is unsubstituted, or is halogen or C ₁ ~ When C ₄ alkyl is substituted), n is 1, 2, 3 or 4, and when n is 2 or more, R ^{1 is} independent of each other and is synonymous with the above.

When n is 1, A is a C ₁ -C ₁₂ alkyl group, and C ₂ -C ₁₂ alkyl group or C ₂ -C ₁₂ alkyl oxygen group which is discontinuously interrupted by one or more O atoms (oxygen atoms). Alkylcarbonylalkyl, C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl, C ₃ -C ₁₂ cycloalkyl-C ₁ -C ₁₂ alkyl -C ₃ ~C ₁₂ cycloalkyl, C ₆ -C ₁₄ aryl, C ₁ -C ₄ alkyl-C ₆ ~C ₁₄ extended aryl, C ₆ ~C ₁₄ aryl-C ₁ ~C ₄ Alkyl-C ₆ -C ₁₄ extended aryl (here, the alkyl group is a straight or branched chain and may be substituted by halogen, C ₃ -C ₁₂ cycloalkyl, C ₃ -C ₁₂ cycloalkyl, C ₆ ~C ₁₄ aryl or C ₆ ~C ₁₄ extended aryl is unsubstituted, or substituted by halogen or C ₁ -C ₄ alkyl), or (meth) propylene decyloxyalkyl, n is 2 In the case, A is a C ₁ -C ₁₂ alkyl group, a C ₂ -C ₁₂ alkyl group which is discontinuously interrupted by one or more O atoms (oxygen atoms), and a C ₁ -C ₁₂ alkyloxy group. Carbonylalkylene, C ₃ ~C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl -C ₃ ~C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl -C ₃ ~C ₁₂ ring extension Alkyl-C ₁ -C ₁₂ alkylene, C ₃ -C ₁₂ cycloalkyl-C ₁ -C ₁₂ alkyl-C ₃ ~C ₁₂ cycloalkyl, two C ₃ ~C ₁₂ cycloalkane diyl, C ₆ ~ C ₁₄ exoaryl, C ₁ ~ C ₄ alkyl - C ₆ ~ C ₁₄ extended aryl - C ₁ ~ C ₄ alkyl, or C ₆ ~ C ₁₄ a group -C ₁ -C ₄ alkyl-C ₆ -C ₁₄ extended aryl (here, the alkyl group is a straight or branched chain and can be substituted by halogen, C ₃ ~ C ₁₂ cycloalkyl or C ₆ ~ Wherein C _{14 is an} aryl group which is unsubstituted or substituted by a halogen or a C ₁ -C ₄ alkyl group), and when n is 3, A is a formula (1) below.

(wherein R ^{2 is the} same or different and is a C ₁ to C ₁₂ alkyl group of a straight or branched chain), and the following formula (2)

(wherein R ^{3 is the} same or different and is a C ₁ to C ₁₂ alkyl group of a straight or branched chain) or the following formula (3)

(wherein R ^{4 is the} same or different and is a C ₁ to C ₁₂ alkyl group of a straight or branched chain, and R ⁵ is CH), and when n is 4, A is a formula (4) below.

Wherein X ³ is Si, or C ₃ -C ₁₂ cycloalkyl-C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl, or C ₆ -C ₁₄ aryl-C ₁ -C _4- alkyl-C ₆ -C ₁₄ aryl (here, the alkyl group is a straight or branched chain and may be substituted by halogen, and the C ₃ -C ₁₂ cycloalkyl or C ₆ -C ₁₄ aryl group is unsubstituted, Or a compound represented by a tetravalent residue derived from a halogen or a C ₁ -C ₄ alkyl group.

The compound of the above formula (I) has at least one of the above a compound of an isocyanate group (-N=C=O), for example, at least one isocyanate compound selected from the group consisting of the above monoisocyanate compound, the above diisocyanate compound, the above triisocyanate compound, and the above tetraisocyanate compound, and a hydrazine or a plurality of It is preferred that the valence amine compound is obtained by a reaction. The compound represented by the above formula (I) is such that the above isocyanate compound and the above-mentioned hydrazine or polyvalent amine compound are relative to the above isocyanate compound 1 The hydrazine or polyvalent amine compound is preferably from 0.01 mol to 50 mol, more preferably from 0.1 mol to 50 mol, more preferably from 0.1 mol to 30 mol, and particularly preferably 0.1 mol. 20 moles, in organic solvent or neat (no solvent), preferably -10 ° C ~ 120 ° C, more preferably -5 ° C ~ 100 ° C, and then better 0 ° C ~ 50 ° C, especially better 5 It is preferred to control the reaction at ~30 ° C.

Further, the compound represented by the above formula (I) is an isocyanate group 1 molar which is an isocyanate compound, a hydrazine compound or a polyvalent amine compound, and a first amine group contained in a hydrazine or a polyvalent amine compound. The total amount is preferably from 0.01 moles to 50 moles, more preferably from 0.1 moles to 50 moles, more preferably from 0.1 moles to 30 moles, and more preferably from 0.5 moles to 20 moles. The winner is also good.

In the present invention, an epoxy resin containing a compound represented by the following formula (Ia) and/or a curing agent for a resin containing at least one unsaturated bond among the compounds represented by the above formula (I) are preferred.

The hardener of the present invention has a compound having at least one first-order amine group in the molecule as the following formula (Ia)

[wherein R ^{1 is} independently a single bond or a C ₁ -C ₁₂ alkyl group, and C _{2 is} discontinuously interrupted by one or more NH (imine groups) or O atoms (oxygen atoms). ~C ₁₂ alkyl (the H atom (hydrogen atom) bonded to the N atom (nitrogen atom) may be substituted by an amine group or a C ₁ -C ₁₂ alkylamine group), C ₃ ~ C ₁₂ ring extension alkyl group, C ₁ ~ C ₁₂ alkylene -C ₃ ~ C ₁₂ cycloalkyl alkylene, C ₁ ~ C ₁₂ alkylene -C ₃ ~ C ₁₂ cycloalkyl alkylene -C ₁ ~ C ₁₂ alkylene, C ₃ ~ C ₁₂ cycloalkyl-C ₁ ~ C ₁₂ alkyl-C ₃ ~ C ₁₂ cycloalkyl, C ₆ ~ C ₁₄ extended aryl, C ₁ ~ C ₄ alkyl - C ₆ ~ C ₁₄ extended aryl, C ₁ ~ C ₄ alkyl - C ₆ ~ C ₁₄ extended aryl - C ₁ ~ C ₄ alkyl, or C ₆ ~ C ₁₄ extended aryl - C ₁ ~ C ₄ alkyl a aryl-C ₆ -C ₁₄ aryl group (here, an alkyl group is a straight or branched chain and may be substituted by halogen, a C ₃ -C ₁₂ cycloalkyl group or a C ₆ -C ₁₄ aryl group is unsubstituted, Or substituted by halogen or C ₁ -C ₄ alkyl), X ¹ is a C ₁ -C ₁₂ alkyl group, and C ₂ ~ C _{12 is} discontinuously interrupted by one or more O atoms (oxygen atoms). Alkyl, C ₁ ~C ₁₂ alkyloxycarbonylalkyl, C ₃ ~C ₁₂ cycloalkyl, C ₁ ~C ₁₂ alkyl - C ₃ ~ C ₁₂ cycloalkyl, C ₁ ~ C ₁₂ alkyl - C ₃ ~ C ₁₂ cycloalkyl - C ₁ ~ C ₁₂ alkyl, C ₃ ~ C ₁₂ cycloalkyl - C ₁ ~C ₁₂ alkylene-C ₃ ~C ₁₂ cycloalkylene, di C ₃ ~C ₁₂ cycloalkane diyl, C ₆ ~C ₁₄ extended aryl, C ₁ ~C ₄ alkyl -C ₆ ~C ₁₄ aryl-C ₁ ~ C ₄ alkyl, or C ₆ ~ C ₁₄ extended aryl - C ₁ ~ C ₄ alkyl - C ₆ ~ C ₁₄ extended aryl (here, alkyl is straight chain or branched and may be substituted with halo, C ₃ ~ C ₁₂ cycloalkyl alkylene or C ₆ ~ C ₁₄ arylene group is unsubstituted, substituted by halogen or C ₁ ~ C ₄ alkyl)] is preferred.

X ¹ in the formula (Ia) is synonymous with A in the case where n is 2 in the formula (I).

The compound represented by the above formula (Ia) is obtained by reacting the above diisocyanate compound with a hydrazine or a polyvalent amine compound. good. The diisocyanate compound and the hydrazine or polyvalent amine compound are preferably from 0.01 moles to 50 moles, more preferably from 0.1 moles to 50 moles, relative to the diisocyanate compound 1 mole, and the hydrazine or polyvalent amine compound. Preferably, the method is 0.1 mol to 30 mol, and particularly preferably 0.1 mol to 20 mol, in an organic solvent or neat (no solvent), preferably -10 ° C to 120 ° C, more preferably - 5 ° C It is better to obtain a reaction at ~100 ° C, preferably from 0 ° C to 50 ° C, and more preferably from 5 to 30 ° C.

The compound obtained by the reaction of the diisocyanate compound with, for example, tris(2-aminoethyl)amine having a polyvalent amine compound having three first-order amine groups in the molecule, for example, is a compound represented by the following formula.

In the above formula, X ^{1 is} synonymous with X ¹ in the formula (Ia).

The compound represented by the above formula (Ia) may, for example, be mentioned.

1,1'-[Methylenebis(cyclohexane-1,4-diyl)]bis[3-(12-aminododedo)urea] (A-1), 1,1'-[ Methylene bis(cyclohexane-1,4-diyl)]bis[3-(2-aminoethyl)urea](A-2), 1,1'-[methylenebis(cyclohexyl) Alkenyl-1,4-diyl)]bis[3-(6-aminohexyl)urea](A-3), 1,1'-(hexane-1,6-diyl)bis[3-( 12-aminododecyl)urea (A-4), 1,1'-(hexane-1,6-diyl)bis[3-(2-aminoethyl)urea](A-5), 1,1'-( Alkan-1,6-diyl)bis[3-(6-aminohexyl)urea](A-6), N,N'-hexamethylene[carbonylbis(ureidodiyl)-2-amino Ethyl]-[carbonylbis(ureidodiyl)-6-aminohexyl](A-7).

The compound represented by the above formula (Ia) may, for example, be a compound represented by the following formula.

In the present invention, an epoxy resin containing a compound represented by the following formula (Ib) and/or a curing agent for a resin containing at least one unsaturated bond among the compounds represented by the above formula (I) are preferred.

The hardener of the present invention has a compound having at least one first-order amine group in the molecule as the following formula (Ib)

(In the formula, X ¹ is synonymous with the above.) The above-mentioned two-half carbolic compound is preferred. X ¹ in the formula (Ib) is synonymous with A in the case where n is 2 in the formula (I).

The compound represented by the above formula (Ib) is preferably obtained by reacting the above diisocyanate compound with a hydrazine. The diisocyanate compound and the hydrazine are relatively diisocyanate compound 1 mole, and the hydrazine is preferably 0.01 mol to 50 mol, more preferably 0.1 mol to 50 mol, and even more preferably 0.1 mol to 30 mol. Preferably, the method is 0.1 mole to 20 moles, in an organic solvent or neat (no solvent), preferably -10 ° C to 120 ° C, more preferably -5 ° C to 100 ° C, and more preferably 0 ° C to 50 ° °C, especially preferably 5~30 °C while controlling the side reaction is better.

In terms of the two halo-carboxy compounds represented by the above formula (Ib), for example

4,4'-(methylenedi-1,4-cyclohexyl) bis(semi-calendar) (B-1), 4,4'-hexamethylene double (semi-calendar) (B-2 ), 4,4'-(2,2,4-trimethylhexamethylene) bis(semi-calendar) (B-3), 4,4'-(1,3-cyclohexyldiamine) Base) double (half-calendar) (B-4), 4,4'-(1,3-phenylene bismethylene) bis(semi-carban) (B-5), 4,4'-iso Fulcone double (half card) (B-6) and the like.

The compound represented by the above formula (Ib) is, for example, a compound represented by the following formula.

The hardener of the present invention contains the following formula (IIa)

[In the formula, R ¹ is a single bond, or a C ₁ to C ₁₂ alkyl group, and C ₂ to C which are discontinuously interrupted by one or more NH (imine groups) or O atoms (oxygen atoms). ₁₂ alkyl group (H atom (hydrogen atom) bonded to N atom (nitrogen atom) may be substituted by an amine group or a C ₁ -C ₁₂ alkylamino group), C ₃ ~ C ₁₂ cycloalkyl group , C ₁ ~ C ₁₂ alkyl-C ₃ ~ C ₁₂ cycloalkyl, C ₁ ~ C ₁₂ alkyl - C ₃ ~ C ₁₂ cycloalkyl - C ₁ ~ C ₁₂ alkyl, C ₃ ~C ₁₂ cycloalkyl-C ₁ ~C ₁₂ alkyl-C ₃ ~C ₁₂ cycloalkyl, C ₆ ~C ₁₄ extended aryl, C ₁ ~C ₄ alkyl -C ₆ ~C ₁₄ an arylene group, C ₁ ~ C ₄ alkylene -C ₆ ~ C ₁₄ arylene group -C ₁ ~ C ₄ alkylene, or C ₆ ~ C ₁₄ arylene group -C ₁ ~ C ₄ alkylene group - C ₆ -C ₁₄ extended aryl (here, the alkyl group is a straight or branched chain and may be substituted by halogen, C ₃ ~ C ₁₂ cycloalkyl or C ₆ - C ₁₄ extended aryl is unsubstituted, or Halogen or C ₁ -C ₄ alkyl group substituted.), X ² is a C ₁ -C ₁₂ alkyl group, a C ₂ -C ₁₂ alkyl group discontinuously interrupted by one or more O atoms (oxygen atoms) , C ₁ -C ₁₂ alkyloxycarbonylalkylene, C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl, C ₃ ~C ₁₂ cycloalkyl-C ₁ ~C ₁₂ alkyl-C ₃ ~C ₁₂ cycloalkyl, C ₆ -C ₁₄ aryl, C ₁ -C ₄ alkyl-C ₆ ~C ₁₄ Aryl, C ₆ -C ₁₄ aryl-C ₁ ~C ₄ alkyl-C ₆ -C ₁₄ extended aryl (here, alkyl is linear or branched and can be substituted by halogen, C ₃ ~ C ₁₂ -cycloalkyl, C ₃ -C ₁₂ cycloalkyl, C ₆ -C ₁₄ aryl or C ₆ -C ₁₄ extended aryl is unsubstituted or substituted by halogen or C ₁ -C ₄ alkyl.) Or (meth) propylene decyloxyalkyl. The compound represented by 〕 is preferred. X ² in the formula (IIa) is synonymous with A in the case where n is 1 in the formula (I).

The compound represented by the above formula (IIa) is preferably obtained by reacting the above monoisocyanate compound with the above-mentioned hydrazine or polyvalent amine compound. The monoisocyanate compound and the hydrazine or polyvalent amine compound are relative to the isocyanate group 1 mol of the monoisocyanate compound, and the amine group of the diamine compound is preferably 0.1 mol to 50 mol, more preferably 0.1 mol to 30 Moer, especially good for 0.1 moles to 20 moles in organic solvents In the middle or neat (no solvent), preferably -10 ° C ~ 120 ° C, more preferably -5 ° C ~ 100 ° C, and then preferably 0 ° C ~ 50 ° C, especially preferably 5 ~ 30 ° C side control side reaction It is better.

In the formula (IIa), when R ¹ is a single bond, it is a semi-calendar compound. The semicarbazone compound is preferably a compound represented by the following formula (IIb).

In the formula, X ² is synonymous with the above. X ² in the formula (IIb) is synonymous with A in the case where n is 1 in the formula (I).

The compound represented by the above formula (IIb) is preferably obtained by reacting the above monoisocyanate compound with a hydrazine. The monoisocyanate compound and the hydrazine are preferably a monoisocyanate compound 1 mol, and the hydrazine is preferably 0.01 mol to 50 mol, more preferably 0.1 mol to 50 mol, and even more preferably 0.1 mol to 30 mol. Preferably, the method is 0.1 mole to 20 moles, in an organic solvent or neat (no solvent), preferably -10 ° C to 120 ° C, more preferably -5 ° C to 100 ° C, and more preferably 0 ° C to 50 ° °C, especially preferably 5~30 °C while controlling the side reaction is better.

The compound represented by the above formula (IIa) is, for example, 4-(ethyl acrylate) semicarbazide (B-7).

The compound represented by the above formula (IIb) is, for example, a compound represented by the following formula.

The hardener of the present invention is contained to contain isocyanic acid by the above a compound obtained by reacting an ester compound with a compound having at least one first-order amine group in a molecule obtained by a reaction with a hydrazine or a polyvalent amine compound having two or more first-stage amine groups in the molecule, and then treating with an isocyanate compound The hardener is also good.

A compound obtained by treating a compound having at least one first-stage amine group in a molecule with an isocyanate compound by a curing agent, and a resin containing a hardener and an epoxy resin and/or having at least one unsaturated bond The liquid stability of the resin composition is improved, and the increase in viscosity with time can be suppressed.

a compound having at least one amine of the first order in the molecule The isocyanate compound to be used in the treatment is a compound having at least one isocyanate group, which is not particularly limited. As the isocyanate compound, at least one selected from the above isocyanate compounds is preferably used. The isocyanate compound may be used singly or in combination of two or more kinds.

Processing a compound having at least one first-order amine group in the molecule The amount of the isocyanate compound to be used is not particularly limited, and may be appropriately selected depending on the purpose and the like. When the amount of the isocyanate compound used is 1 mole per mole of the compound having at least one first-stage amine group in the molecule, the isocyanate group has an isocyanate group number of preferably 0.01 mol to 10 mol, and is 0.02. The molar amount of ~5 moles is better, and it is better to be 0.05 moles to 2 moles.

a compound having at least one amine of the first order in the molecule The isocyanate compound is treated in an organic solvent or neat (solvent free), preferably -10 ° C to 120 ° C, more preferably -5 ° C to 100 ° C, still more preferably 10 ° C to 90 ° C, and particularly preferably 20 ° C. It is better to control the side under ~80 °C. The treatment time can be, for example, 0.1 to 100 hours, preferably 0.5 to 50 hours. The heating and mixing time varies depending on the temperature at which heating and mixing are performed. The higher the temperature, the shorter the time, and the lower the temperature, the longer the time. Therefore, the optimum treatment time can be selected in accordance with the purpose of use as a curing agent.

The hardener of the present invention contains the isocyanate by the above a compound having at least one first-order amine group in a molecule obtained by a reaction with a hydrazine or a polyvalent amine compound having two or more amine groups in the molecule, and then an isocyanate compound and an epoxy resin. It is also preferred to treat the resulting compound as a hardener.

The hardener comprises a compound obtained by treating a compound having at least one first-stage amine group in the molecule with an isocyanate compound and an epoxy resin, and contains a hardener and an epoxy resin and/or has at least one unsaturated bond. The liquid resin stability of the resin composition of the resin is improved, and the increase in viscosity over time can be suppressed.

The isocyanate compound used for the treatment of the compound having at least one first-stage amine group in the molecule is not particularly limited as long as it has at least one isocyanate group. As the isocyanate compound, at least one selected from the above isocyanate compounds can be preferably used. The isocyanate compound may be used singly or in combination of two or more kinds.

a compound having at least one amine of the first order in the molecule The epoxy resin to be used in the treatment is a compound having at least one epoxy group, and is not particularly limited, and can be suitably selected from known epoxy resins. Epoxy resin, such as bisphenol A epoxy resin, bisphenol F epoxy resin, bisphenol AD epoxy resin, phenol novolak epoxy resin, cresol novolak epoxy resin, cyclic fat Group epoxy resin, epoxy propyl ester epoxy resin, epoxy propyl amine epoxy resin, heterocyclic epoxy resin, urethane modified epoxy resin, and the like. Among these, bisphenol A type epoxy resin, epoxy propyl ester type epoxy resin, etc. are preferable. Epoxy resins may be used singly or in combination of two or more kinds.

Processing a compound having at least one first-order amine group in the molecule The amount of the isocyanate compound to be used is not particularly limited, and may be appropriately selected depending on the purpose and the like. When the amount of the isocyanate compound used is 1 mole of the number of amine groups of the compound having at least one first-stage amine group in the molecule, the isocyanate group has an isocyanate group number of preferably 0.01 mol to 10 mol. 0.02 moles to 5 moles is better, and it is better to be 0.05 moles to 2 moles.

Processing a compound having at least one first-order amine group in the molecule The amount of the epoxy resin to be used is not particularly limited, and may be appropriately selected depending on the purpose and the like. When the amount of the epoxy resin used is 1 mol of the number of amine groups of the compound having at least one first-order amine group in the molecule, the epoxy group has an epoxy group number of 0.001 mol to 10 mol. It is better to be 0.005 moles to 1 mole, and it is better to be 0.01 moles to 0.5 moles.

a compound having at least one amine of the first order in the molecule The isocyanate compound and the epoxy resin are treated in an organic solvent or neat (solvent free), preferably -10 ° C to 120 ° C, more preferably -5 ° C to 100 ° C, and even more preferably 10 ° C to 90 ° C, especially It is better to carry out the control at 20 ° C ~ 80 ° C. The treatment time can be, for example, 0.1 to 100 hours, preferably 0.5 to 50 hours. The time for heating and mixing varies depending on the temperature at which heating and mixing are performed. The higher the temperature, the shorter the time, and the longer the temperature is, the longer the time is. Therefore, the optimum treatment time can be selected in accordance with the purpose of use as a curing agent.

The hardener of the present invention is contained by using the above isocyanate a compound having at least one first-order amine group in a molecule obtained by a reaction of a compound, a hydrazine or a polyvalent amine compound having two or more first-stage amine groups in a molecule, and then an isocyanate compound and a compound having a hydroxyl group It is also preferred to treat the resulting compound as a hardener.

The curing agent contains a compound obtained by treating a compound having at least one first-stage amine group in the molecule with an isocyanate compound and a compound having a hydroxyl group, and contains a hardener and an epoxy resin and/or has at least one unsaturated bond. The liquid stability of the resin composition of the knot resin is improved, and the increase in viscosity over time can be suppressed.

The isocyanate compound used for the treatment of the compound having at least one first-stage amine group in the molecule is not particularly limited as long as it has at least one isocyanate group. As the isocyanate compound, at least one selected from the above isocyanate compounds can be preferably used. The isocyanate compound may be used singly or in combination of two or more kinds.

a compound having at least one amine of the first order in the molecule The compound having a hydroxyl group to be used in the treatment is not particularly limited and may be appropriately selected from known compounds. Specific examples of the compound having a hydroxyl group include an alcohol compound, a phenol compound, a carboxylic acid compound and the like. The compound having a hydroxyl group may be a monofunctional compound or a polyfunctional compound.

Among the alcohol compounds, in the case of monool compounds, such as Alcohol, ethanol, 1-propanol, isopropanol, 1-butanol, 2-butanol, isobutanol, tert-butyl alcohol, 3-methyl-2-butanol, tert-pentanol, 2, 4-dimethyl-3-pentanol, 3-ethyl-3-pentanol, 3-methyl-3-pentanol, pentaerythritol, 3-pentanol, 2-propan-1-ol, trimethyldecane Methanol, allyl alcohol, 2-bromoethanol, 3-ethyl-2-methyl-3-pentanol, 2-iodoethanol, 1-methoxy-2-propanol, acetone cyanohydrin, (R )-(-)-1-methoxy-2-propanol, 3-pentyn-1-ol, 3-butyn-2-ol, 3-butyn-2-ol, (R)-(+ )-3-butyn-2-ol, (S)-(-)-3-butyn-2-ol, (R)-(+)-3-butyn-2-ol, ethyl cyanohydrin , 3,3-dimethyl-1-butanol, 2,2-difluoroethanol, methyl glycolate, 4-heptanol, 3-hexanol, 3-hexyn-1-ol, 3-methyl 1-butanol, (S)-(-)-2-methyl-1-butanol, DL-2-methyl-1-butanol, 2-methyl-3-butyn-2-ol, 4-methyl-4-heptanol, 2-methyl-2-pentanol, 2-pentanol, (S)-(+)-2-pentanol, (R)-(-)-2-pentanol , 2,2,2-trifluoroethanol, 2,2,2-trichloroethanol, 2,2,2-tribromoethanol, 3-trimethyldecyl-2-propan-1-ol, 1-bromo 2-propanol, 1-buten-3-ol, 2-butyn-1-ol, 1-chloro-2-propanol, cycloglycan , cyclobutanol, 1-chloro-2-methyl-2-propanol, 1,3-dibromo-2-propanol, 1,3-dichloro-2-propanol, 2,6-dimethyl -4-heptanol, 2,2-dimethyl-3-hexanol, 2,5-dimethyl-3-hexanol, 3,5-dimethyl-3-hexanol, 2-ethyl- 1-butanol, 1-heptanol, 2-heptanol, 3-heptanol, 1-hexanol, 2-hexyl Alcohol, hydroxyacetone, 3-methoxy-1-butanol, 2-methyl-3-buten-2-ol, 4-methyl-2-pentanol, 1-nonanol, 1-nonanol, 1-octanol, 1-dodecyl alcohol, 3,7-dimethyl-1-octanol, 1-tetradecanol, 1-undecyl alcohol, 1-hexadecanol, 1-octadecyl alcohol, 1- Pentadecyl alcohol, 2-octanol, 1-docosanol, 1-eicocarbon alcohol, cyclohexane methanol, cyclododecanol, cyclohexaneethanol, 2,5-dimethylcyclohexanol, 2-methylcyclohexanol, 1-cyclohexyl-1-butanol, 2-ethylcyclohexanol, 4-(2-hydroxyethyl)cyclohexanol, 1-cyclohexyl-1-pentanol, 9 -decen-1-ol, oleyl alcohol, 4-cyclohexylcyclohexanol, 2-cyclohexylcyclohexanol, decahydro-2-naphthol, 1-decen-3-ol, 1-decene- 3-alcohol, 3,5-dimethyl-1-adamantane methanol, 8-dimethylamino-1-octyl alcohol, 4-(hydroxymethyl)cyclohexanecarboxylic acid, trans-4-(hydroxyl Methyl)cyclohexanecarboxylic acid, 4-(trifluoromethyl)cyclohexanemethanol, borneol, 2-(benzyloxy)ethanol, and the like.

Further, for example, 2-methoxyethanol, diethylene glycol monomethyl ether, decaethylene glycol monomethyl ether, dodecaethylene glycol monomethyl ether, 3-methoxy-1-propane may also be mentioned. Alcohol, 1-butoxy-2-propanol, pentaethylene glycol monomethyl ether, triethylene glycol monomethyl ether, tetraethylene glycol monomethyl ether, 1,4-butanediol monomethyl A monool compound having an ether bond such as an ether.

In terms of diol compounds, such as ethylene glycol, 1,3-propanediol, 1,4-butanediol, 2,3-butanediol, 2,3-dimethyl-2,3-butanediol, 2,2-Dimethyl-1,3-propanediol, 2-methyl-1,3-propanediol, (S,S)-(+)-2,3-butanediol, pinacol , 2,2-dimethyl-1,3-propanediol, 1,7-heptanediol, 1,5-pentanediol, (S)-(+)-1,2-propanediol , (R)-(-)-1,2-propanediol, 1,5-pentanediol, (S)-(+)-1,2-propanediol, (R)-(-)- 1,2-propanediol, 2-butyne-1,4-diol, 1,6-hexanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1, 12-dodecanediol, 1,2-decanediol, 1,2-tetradecanediol, 1,4-cyclohexanedimethanol, neopentyl glycol, 3,9-double (1 ,1-dimethyl-2-hydroxyethyl)-2,4,8,10-tetraoxaspiro[5.5]undecane, 1,3-bis(2-hydroxyethoxy)benzene, 1, 4-bis(2-hydroxyethoxy)-2-butyne, diethylene glycol, tripropylene glycol, 2,2-bis(4-hydroxycyclohexyl)propane, and the like.

Examples of the triol compound include 1,1,1-tris(hydroxymethyl)ethane, glycerin, 1,2,8-octanetriol, and the like.

Further, examples of the tetrafunctional or higher polyhydric alcohol compound include dipentaerythritol, diglycerin, and Span20.

Among the phenolic compounds, examples of the monofunctional phenol compound include 4-methoxyphenol, 3-chlorophenol, 4-chlorophenol, p-cresol, m-cresol, o-cresol, 3,5- Dichlorophenol, guaiacol, 4-bromophenol, 2,6-dichlorophenol, 4-fluorophenol, 4-iodophenol, 3-methoxyphenol, 3,5-dimethoxyphenol, 4 -Phenoxyphenol, 3-bromophenol, 2-bromophenol, 2,4-dichlorophenol, 3,4-dichlorophenol, 2,6-dimethoxyphenol, 2,6-dimethylphenol , 3,5-dimethylphenol, 2-fluorophenol, 3-fluorophenol, 2-iodophenol, 3-iodophenol, 4-methoxy-1-naphthol, 2,4,6-trichlorophenol , 4-aminophenol, 6-bromo-2-naphthol, 4-chloro-1-naphthol, 2,3-dichlorophenol, 2,5-dichlorophenol, 2,4-dimethylphenol, 3,4-dimethylphenol, 2,6-difluorophenol, 3,5-difluorophenol, 2,6-dibromophenol, 3,5-dibromophenol, 2,4,6-trimethyl Phenol, 4-aminophenolate, 4-tert-butylphenol, 4-tert-butoxyphenol, 4-hydroxybenzonitrile, 2,4-dibromophenol, 2,3-dimethyl Phenol, 2,4-difluorophenol, 3,4-difluorophenol, 3,4-dimethoxyphenol, 4-ethylphenol, 4-ethoxyphenol, 4-hydroxybenzene Aldehyde, 4-hydroxybenzenethiol, 4-isopropylphenol, 4-(methylthio)phenol, 2,4,6-tribromophenol, 2,4,6-triiodophenol, 2,3, 6-trichlorophenol, 5-amino-2-naphthol, 6-amino-1-naphthol, 3-aminophenol, 1-bromo-2-naphthol, 3-bromo-2-naphthol, 2,4-Dichloro-1-naphthol, 1,6-dibromo-2-naphthol, 2,5-difluorophenol, 2,3-difluorophenol, 4-hydroxybenzotrifluoride, 3 -hydroxyphenylthiol, pentachlorophenol, 4-propylphenol, 2,3,4,6-tetrachlorophenol, 2,4,5-trichlorophenol, 2-aminophenol, 5-amino-1 -naphthol, 8-amino-2-naphthol, 4-tert-pentylphenol, 3-tert-butylphenol, 4-sec-butylphenol, 3-cyanophenol, 3-ethoxyphenol, 3-ethylphenol, 2-ethoxyphenol, 3-hydroxybenzaldehyde, 4-benzylphenol, 6-hydroxy-2-naphthonitrile, 6-hydroxy-2-naphthaldehyde, 3-isopropyl Phenol, 2,3,5-trimethylphenol, 2,3,6-trimethylphenol, 4-(trifluoromethoxy)phenol, 4-amino-1-naphthol hydrochloride, 2- Aminophenolate 2-tert-butylphenol, 4-butylphenol, 4-α-cumylphenol, 2-cyanophenol, 2,4-dibromo-1-naphthol, 3-( Dimethylamino)phenol, 2-ethylphenol, 4'-hydroxyacetophenone, 4-hexylphenol, 2-hydroxybenzotrifluoride, 2-hydroxybenzenethiol, 2-isopropyl Phenol, 2-(methylthio)phenol, 4-pentylphenol salicylaldehyde, 3-hydroxybenzotrifluoride, 2,3,5,6-tetrafluorophenol, 2,3,4-trifluoro Phenol, 2-chlorophenol, etc.

In terms of a phenol compound having two hydroxyl groups, for example, 4,4'-dihydroxydiphenyl ether, 5-methoxy resorcinol, 2-methyl resorcinol, 5-methyl resorcinol monohydrate, 5-methylisophthalene Phenol (anhydrous), chlorohydroquinone, 4-chlorocatechol, 2,2'-dihydroxydiphenyl ether, 1,3-bis(4-hydroxyphenoxy)benzene, 5-bromo-m-phenylene Diphenol, 4-chlororesorcinol, 3-chlorocatechol, 4,6-dichlororesorcinol, 2-iodoresorcinol, methyl hydroquinone, 4-methyl catechu Phenol, 3-methoxycatechol, methoxy pair Hydroquinone, 4-bromoresorcinol, 1,4-bis(3-hydroxyphenoxy)benzene, bromohydroquinone, 4-bromocatechol, 2,6-dimethyl-p-phenylene Phenol, 2,5-dimethylresorcinol, 2,3-dimethylhydroquinone, 4-fluorocatechol, 4-fluororesorcinol, 3-methylcatechol, four Chlorohydroquinone, 4,4'-dihydroxydiphenylmethane, 3-bromocatechol, cresol (heterosome mixture), bis(4-hydroxyphenyl) sulfide, 2,6-dibromo -1,5-dihydroxynaphthalene, 3-fluorocatechol, 2,4,6-tribromoresorcinol, 2,2-bis(4-hydroxyphenyl)propane, 4,4'-Asian A bifunctional phenol compound such as bisphenol, trimethylhydroquinone or 1,2-dihydroxynaphthalene, or a monofunctional phenol compound such as 4-hydroxybenzyl alcohol.

As the trifunctional phenol compound, for example, 1,2,4-trihydroxyl group Benzene, 1,8,9-trihydroxyindole, 5-methylpyrrolol, 4,4',4"-trihydroxytriphenylmethane, and the like.

Examples of the tetrafunctional phenol compound include, for example, Leucoquinizarine, and examples of the hexafunctional phenol compound include hexahydroxybenzene, 2,3,6,7,10,11-hexahydroxytriphenylene hydrate.

Examples of the carboxylic acid compound include methoxyacetic acid and B. Aldehydic acid, heptanoic acid, decanoic acid, decanoic acid, lauric acid, myristic acid, 4-methyl-n-octanoic acid, pimelic acid, heptadecanoic acid, 16-hydroxyhexamethylene acid, 15-hydroxypentadecanoic acid, palmitic acid, pentadecanoic acid, stearic acid, behenic acid, arachidic acid, behenic acid, 12-hydroxystearic acid, 2-hexyldecanoic acid, etc. a tricarboxylic acid such as a monocarboxylic acid, azelaic acid, a suberic acid, azelaic acid, (+)-camphoric acid or dodecanedioic acid, or a trifunctional or higher compound such as 1,3,5-pentanetricarboxylic acid Polycarboxylic acid, etc.

The compound having a hydroxyl group may be one type or two or more types. Used together. Among these, at least one selected from the group consisting of an alcohol compound (preferably a diol compound) and a phenol compound is preferred.

Processing a compound having at least one first-order amine group in the molecule The amount of the isocyanate compound to be used is not particularly limited, and may be appropriately selected depending on the purpose and the like. When the amount of the isocyanate compound used is one mole of the compound having at least one first-stage amine group in the molecule, the number of isocyanate groups of the isocyanate compound is preferably from 0.01 mol to 10 mol, and is 0.02. The molar amount of ~5 moles is better, and it is better to be 0.05 moles to 2 moles.

Processing a compound having at least one first-order amine group in the molecule The amount of the compound having a hydroxyl group of the substance to be used is not particularly limited, and may be appropriately selected depending on the purpose and the like. When the amount of the compound having a hydroxyl group is 1 mol of the compound having at least one first-order amine group in the molecule, the number of hydroxyl groups is preferably 0.001 mol to 10 mol, and is 0.005 mol. The amount of ear ~1 mole is better, and it is better to be 0.01 mole to 0.5 mole.

a compound having at least one amine of the first order in the molecule The isocyanate compound and the compound having a hydroxyl group are treated in an organic solvent or neat (solvent free), preferably -10 ° C to 120 ° C, more preferably -5 ° C to 100 ° C, still more preferably 10 ° C to 90 ° C, It is better to carry out the control at 20 ° C ~ 80 ° C. The treatment time can be, for example, 0.1 to 100 hours, preferably 0.5 to 50 hours.

[Resin composition]

The resin composition of the present invention contains at least one first-order amine group in a molecule obtained by a reaction of the above isocyanate compound, a hydrazine or a polyvalent amine compound having two or more first-stage amine groups in the molecule. The hardener (A) of the compound and the epoxy resin and/or the resin (B) having at least one unsaturated bond in the molecule. The curing agent (A) is preferably a compound represented by at least one selected from the group consisting of the above formulas (I), (Ia), (Ib), (IIa) and (IIb), and contains such a compound. A compound treated with an isocyanate compound, an isocyanate compound, an epoxy resin, or an isocyanate compound and a compound having a hydroxyl group is also preferred.

[epoxy resin]

For epoxy resin, well-known ones can be used, such as bisphenol A epoxy resin, bisphenol F epoxy resin, bisphenol AD epoxy resin, phenol novolak epoxy resin, cresol novolac epoxy Resin, cyclic aliphatic epoxy resin, glycidyl propyl ester resin, epoxypropylamine epoxy resin, heterocyclic epoxy resin, urethane modified epoxy resin, and the like. Among these, a bisphenol A type epoxy resin, a cresol novolak type epoxy resin, or the like is preferably used. An epoxy (meth)acrylic acid modified with a (meth)acrylic acid resin having a glycidyl group can also be used. For example, a partially esterified epoxy resin obtained by reacting an epoxy resin described in JP-A-2012-77202 with (meth)acrylic acid is preferred. Specifically, if one equivalent of the epoxy group is used, the (meth)acrylic acid is preferably 10 to 90 equivalent %, more preferably 20 to 80 equivalent %, still more preferably 30 to 70 equivalent %, and particularly preferably 40. ~60 equivalent % of (meth)acrylic acid reacted A esterified epoxy resin is preferred. The epoxy resin may be used singly or in combination of two or more. Further, it may be an epoxy resin containing an unsaturated bond.

Partially esterified epoxy resin, for example, first, to make bisphenol A The epoxy resin and the acrylic acid or methacrylic acid are reacted in a conventional manner in the presence of a basic catalyst in an amount of 2 equivalents to the epoxy group, and the carboxylic acid group is 0.9 to 1.1 equivalents, and the reaction product is added in a mass ratio of about 4 times of toluene and the same amount of pure water were stirred at 60 to 80 ° C for 1 hour, and after standing, separated into an organic layer and an aqueous layer, and the aqueous layer was removed. By repeating this operation 3 to 5 times, the organic layer is finally recovered, and the residual toluene is removed by vacuum distillation, and a partially esterified epoxy resin reduced in water-soluble ionic substance is obtained. Specific examples of the bisphenol A type epoxy resin include EPIKOTE 828, 834, 1001, 1004 (manufactured by Mitsubishi Chemical Corporation), EPICLON 850, 860, and 4055 (manufactured by DIC Corporation). In the case of such a raw material resin, a resin which is subjected to a reduction treatment of a water-soluble ionic substance (hereinafter referred to as a high-purification treatment), for example, EPICLON 850S (manufactured by DIC Corporation) or the like is preferable.

[Resin having at least one unsaturated bond in the molecule]

The resin composition may contain a resin having at least one unsaturated bond in the molecule. The resin having at least one unsaturated bond in the molecule, for example, a styrene derivative, an ethylene derivative, a maleimide derivative, a (meth)acrylic acid derivative, or the like. Among them, a (meth)acrylic acid derivative having at least one (meth)acryl fluorenyl group in the molecule is preferably used.

(meth)acrylic acid derivatives, such as (meth) methacrylate, ethyl (meth) acrylate, n-butyl (meth) acrylate, isobutyl (meth) acrylate, t-butyl (meth) acrylate, etc. Alkyl ester; aryl (meth) acrylate such as phenyl (meth) acrylate; arylalkyl (meth) acrylate such as benzyl (meth) acrylate; methoxy (meth) acrylate An alkoxyalkyl (meth)acrylate such as an ester, ethoxyethyl (meth)acrylate, propoxyethyl (meth)acrylate or butoxyethyl (meth)acrylate; Hydroxy group containing 2-hydroxyethyl methacrylate, 3-hydroxypropyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, etc. (Meth) acrylate; (meth) acrylate such as cyclohexyl methacrylate. Here, (meth)acrylic means both acrylic acid and methacrylic acid.

And epoxy resin with at least one unsaturated in the molecule In the case of a bonded resin, the amount of the epoxy resin combined with the resin having at least one unsaturated bond in the molecule can be appropriately determined in accordance with the purpose of the hardened body in which the resin composition is cured. When the resin having at least one unsaturated bond in the molecule is a (meth)acrylic acid derivative having at least one (meth)acryloyl group in the molecule, (meth)acrylic acid is equivalent to 1 equivalent of the epoxy group. The thiol group is preferably 0.1 to 9.0 equivalents, and the (meth) acrylonitrile group is preferably 0.3 to 4.0 equivalents.

The resin composition may contain an anthrone resin, a urea resin, a quinone imine resin, glass, etc., in addition to the above-mentioned resin.

Moreover, the resin composition may be combined with various additives as necessary, such as an antioxidant, an ultraviolet absorber, a light stabilizer, and a decane coupling. Agent, coating surface modifier, thermal polymerization inhibitor, flat agent, surfactant, colorant, preservation stabilizer, plasticizer, slip agent, filler, inorganic particles, aging inhibitor, wettability improver, antistatic agent Wait.

The above hardener (A) and epoxy resin and/or intramolecular The amount of the resin (B) having at least one unsaturated bond is preferably 0.001 to 1 equivalent to the epoxy resin, and the total amount of the semi-carboxy group or the first amine group of the hardener (A). 10 equivalents, more preferably 0.01 to 8 equivalents, still more preferably 0.05 to 5 equivalents, still more preferably 0.1 to 3 equivalents. When the total amount of the epoxy group is 1 equivalent to the epoxy group, and the total amount of the semi-carboxy group or the first-stage amine group of the hardener (A) is 0.1 to 3 equivalents, the resin composition is contained in a sealant such as a liquid crystal display panel. In the case of the thinning of the sealant, the versatility of the adhesion to a plurality of adherends, etc., it is possible to exhibit the ability to suppress the cutting of the unit cell and the mounting of the IC for driving the liquid crystal cell. Peel strength of peeling.

The above hardener (A) and epoxy resin and/or intramolecular The amount of the resin (B) having at least one unsaturated bond is independently contained in the epoxy resin (B) or the epoxy resin and the resin (B) having at least one unsaturated bond in the molecule. In the case of the epoxy group, the epoxy group is equivalent to 1 equivalent of the epoxy group, and the total amount of the semi-carboxy group or the first-stage amine group of the hardener (A) is preferably 0.0005 to 10 equivalents, more preferably 0.005 to 8 equivalents. It is 0.025 to 5 equivalents, and particularly preferably 0.05 to 3 equivalents.

Further, in the case where the resin (B) having at least one unsaturated bond in the molecule is contained alone, the unsaturated bond of the resin (B) is equivalent to 1 equivalent, and the hardener (A) is a half-calendar or the first stage. The total amount of amine groups should be 0.0005 to 10 equivalents, more preferably 0.005 to 8 equivalents, still more preferably 0.025 to 5 equivalents, and particularly preferably 0.05 to 3 equivalents. When the amount of the curing agent (A) of the resin (B) is within the above range, the resin composition is contained in a sealing agent such as a liquid crystal display panel, and can be adapted to the thinning of the sealant and to a plurality of adherends. In addition, it is possible to exhibit the adhesion strength which can suppress the peeling of the unit cell and the peeling of the IC for driving the liquid crystal cell.

[Liquid Crystal Sealant Composition]

The present invention is a liquid crystal sealant composition containing the above resin composition. The liquid crystal sealant composition contains a resin composition containing the above-mentioned hardener (A) and an epoxy resin and/or a resin (B) having at least one unsaturated bond in the molecule, and a photopolymerization initiator (C). It is preferred to use other inorganic fillers (D) as necessary.

[Photopolymerization initiator (C)]

Examples of the photopolymerization initiator include benzophenone, 2,2-diethoxyacetophenone, benzyl ester, benzhydryl isopropyl ether, benzyldimethylketal, and 1-hydroxyl group. Cyclohexyl phenyl ketone, thioxanthone, and the like. Further, as the photopolymerization initiator, a commercially available photoradical polymerization initiator can be used. Commercially available photoradical polymerization initiators include, for example, IRGACURE 907, IRGACURE 819, IRGACURE 651, IRGACURE 369, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, and Lucirin TPO (all manufactured by BASF Japan Co., Ltd.).

[Inorganic Filler (D)]

The inorganic filler is not particularly limited, and examples thereof include spherical cerium oxide, spherical alumina, spherical titanium oxide, spherical alumina, and spherical calcium carbonate. Among them, spherical cerium oxide is preferred because it is excellent in dispersibility, adhesion to a sealing agent suitable for a liquid crystal dropping method, and excellent in moisture resistance of a cured product.

The ratio of the components of the liquid crystal sealant composition is from 0.5 to 5 parts by mass, preferably from 0.5 to 4 parts by mass, more preferably from 0.8 to 5 parts by mass, based on 100 parts by mass of the resin composition. 3 parts by mass, (D) the inorganic filler is 0 to 40 parts by mass, preferably 2 to 30 parts by mass, more preferably 3 to 20 parts by mass. Further, among the total mass of the liquid crystal sealant composition, (C) the photopolymerization initiator is preferably 0.5 to 3% by mass, and (D) the inorganic filler is preferably 0 to 40% by mass.

The liquid crystal sealant composition particularly pays attention to the uniformity and complete dispersion of the solid matter such as the inorganic filler, and is preferably produced by thorough kneading using a paint roller or the like.

[Liquid Crystal Display Panel]

In addition to the requirements for diversification of the thinning and the adhesion, the liquid crystal sealing agent composition of the present invention can exhibit the peeling strength of the peeling of the cell when the cell is cut out and the IC for driving the liquid crystal cell. It can be applied to the manufacture of liquid crystal display panels.

That is, the liquid crystal display panel of the present invention is provided with a facing glass base. A cured product of a liquid crystal sealant composition of a plate and a subsequent glass substrate, and a liquid crystal sealed with a cured product of a facing glass substrate and a liquid crystal sealant composition.

[Method of Manufacturing Liquid Crystal Display Panel]

The liquid crystal display panel can be produced by photohardening using the liquid crystal sealant composition of the present invention, followed by thermal curing. Fig. 1 shows an embodiment of manufacturing a liquid crystal display panel. Specifically, as shown in the cross-sectional view of Fig. 1(a), the liquid crystal sealant composition 2 of the present invention is applied to one of the glass substrates 1 as shown in the cross-sectional view of Fig. 1(b). . Next, as shown in the cross-sectional view of FIG. 1(c), another glass substrate 4 is disposed oppositely on the liquid crystal sealant composition 2 on one of the glass substrates 1, and ultraviolet rays or the like are irradiated under pressure. After the irradiation of 1,000 to 3,000 mJ, the liquid crystal sealant composition 2 is cured, and the pair of glass substrates 1 and 4 are bonded together, and then heated at a temperature of 100 to 120 ° C for about 1 hour without full pressure, and sufficiently hardened. The liquid crystal sealing unit cell 5 surrounded by the pair of glass substrates 1 and 4 and the cured liquid crystal sealing agent 2 is formed. In the cell 5, as shown in the plan view of Fig. 1(d), the liquid crystal 6 is injected from the liquid crystal injection hole 3 in a vacuum, and the liquid crystal injection hole 3 is sealed to manufacture the liquid crystal display panel 7. The liquid crystal sealing composition is subjected to dispensing coating on an ITO glass substrate with a rubbing treatment alignment film, and then the liquid crystal is dropped on the substrate, and the upper and lower substrates are bonded by a liquid crystal dropping method (ODF method), and irradiated with ultraviolet rays (for example) Illumination and irradiation time: 1000 mJ, 100 mW/cm ² /365 nm, 50 mJ, and 50 mW/cm ² /365 nm for 1 second), and then hardening for 1 hour, for example, in a hot air oven at 120 ° C for 1 hour. .

[Examples]

Hereinafter, the present invention will be specifically described by way of examples, but the invention is not limited to the examples.

[Synthesis of hardener] (Example 1)

(B-1) 4,4'-(methylenedi-1,4-cyclohexyl) bis(semi-calendar)

A solution A in which 13.05 g of dicyclohexylmethane-4,4'-diisocyanate was dissolved in 75 g of ethanol and a solution B in which 5 g of hydrazine was dissolved in 75 g of ethanol were prepared. The solution B was placed in a flask, and controlled and stirred at 25 ° C to cause the solution A to drip at a rate of 1.4 g/min. After completion of the dissolution liquid A dropping, the reaction solution was Fourier transform infrared spectroscopy measurement confirmed no peak near the isocyanate groups from 2250cm ^-1 to complete the reaction. 1 mol of dicyclohexylmethane-4,4'-diisocyanate was reacted in such a manner that the hydrazine became 2 mol (mole ratio 1:2).

After the completion of the reaction, the filter was filtered using a filter paper (No. 4, manufactured by Kiriyama Co., Ltd.), and degreased. The extract was washed with 50 ml of distilled water, and then filtered, and the obtained filtrate was dried in a vacuum oven at 50 °C.

After drying, it was pulverized by a high-pressure pulverizer (trade name: nano jet mill, manufactured by Aishin Nanotech Co., Ltd.) to produce a ruthenium compound having an average particle diameter (median diameter) of 2.0 μm.

In addition, the average particle diameter (median diameter) was measured using a particle size distribution meter (LA-950V2: manufactured by Horiba, Ltd.).

(Example 2) (B-2) 4,4'-hexamethylene double (half card)

A solution A in which 16.8 g of hexamethylene diisocyanate was dissolved in 150 g of ethanol and a solution B in which 10 g of hydrazine was dissolved in 150 g of ethanol were prepared. The solution B was controlled and stirred at 25 ° C, and the solution A was dropped at a rate of 1.4 g / minute. After the completion of the dropwise addition of the solution A, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. 1 mol of hexamethylene diisocyanate was reacted in such a manner that the hydrazine became 2 mol (molar ratio 1:2).

After the completion of the reaction, the filter was filtered using a filter paper (No. 4, manufactured by Kiriyama Co., Ltd.), and degreased, and the obtained filtrate was washed with 50 ml of ethanol, and then filtered to obtain a filtration. Take The vacuum oven was dried at 50 °C. After drying, it was pulverized by a high-pressure pulverizer (trade name: nano jet mill, manufactured by Aishin Nanotech Co., Ltd.) to produce a ruthenium compound having an average particle diameter (median diameter) of 2.1 μm.

(Example 3) (B-7) 4-(ethyl acrylate) half-calendar

A solution A of 14.1 g of 2-isocyanoethoxyethyl acrylate was dissolved in 150 g of ethanol, and a solution B in which 5 g of hydrazine was dissolved in 150 g of ethanol was prepared. The solution B was controlled and stirred at 25 ° C, and the solution A was dropped at a rate of 1.4 g / minute. After the completion of the dropwise addition of the solution A, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. The reaction was carried out in such a manner that the hydrazine became 1 mol (1:1 molar ratio) relative to 2-isocyanooxyethyl acrylate 1 mol.

After completion of the reaction, the ethanol was removed by an evaporator at 50 ° C, and the purified product was measured by a Fourier transform infrared spectrometer. It was confirmed that there was no peak near 3300 cm ^{-1 of} ethanol, and a liquid ruthenium compound was produced.

(Example 4) (B-3) 4,4'-(2,2,4-trimethylhexamethylene) bis(semi-calendar)

A solution A in which 10.51 g of trimethyl hexane methylene diisocyanate was dissolved in 50 g of ethanol and a solution B in which 5.01 g of hydrazine was dissolved in 50 g of ethanol were prepared. The solution B was controlled and stirred at 25 ° C, and the solution A was dropped at a rate of 1.4 g / minute. After the completion of the dropwise addition of the solution A, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. 1 mol of trimethylhexamethylene diisocyanate was reacted in such a manner that the hydrazine became 2 mol (molar ratio 1:2).

After completion of the reaction, the ethanol was removed by an evaporator at 50 ° C, and the purified product was measured by a Fourier transform infrared spectrometer. It was confirmed that there was no peak near 3300 cm ^{-1 of} ethanol, and a liquid ruthenium compound was produced.

(Example 5) (B-5) 4,4'-(1,3-phenylene bismethylene) bis(semi-calendar)

A solution A in which 18.82 g of m-fluorene diisocyanate was dissolved in 100 g of isopropyl alcohol and a solution B in which 25.3 g of hydrazine was dissolved in 100 g of isopropyl alcohol were prepared. In a three-necked flask, the solution B was stirred while being controlled at 30 ° C, and the solution A was dropped at a rate of 1.4 g/min. After the completion of the dropwise addition of the solution A, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. Relative to m-fluorene diisocyanate 1 mole, the reaction was carried out in such a manner that the hydrazine became 5 moles (mole ratio 1:5).

After the completion of the reaction, the filter paper (manufactured by Kiriyama Co., Ltd.) was used for filtration, and the solution was degreased, and the obtained filtrate was washed with 50 ml of isopropyl alcohol, and then filtered. The resulting filtrate was dried in a vacuum oven at 50 °C.

After drying, it was pulverized by a high-pressure pulverizer (trade name: nano jet mill, manufactured by Aishin Nanotech Co., Ltd.) to produce a ruthenium compound having an average particle diameter (median diameter) of 2.2 μm.

(Example 6) (B-4) 4,4'-(1,3-cyclohexyl bismethylene) bis(semi-calendar)

A solution A in which 19.42 g of 1,3-bis(isocyanatomethyl)cyclohexane was dissolved in 100 g of isopropyl alcohol and a solution B in which 25.3 g of a hydrazine was dissolved in 100 g of isopropyl alcohol were prepared. In a three-necked flask, the solution B was stirred while being controlled at 30 ° C, and the solution A was dropped at a rate of 1.4 g/min. After the completion of the dropwise addition of the solution A, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. The reaction was carried out in such a manner that 1,3 bis(isocyanatomethyl)cyclohexane was 1 mol, and the hydrazine was 5 mol (mole ratio 1:5).

After the completion of the reaction, the filter paper (manufactured by Kiriyama Co., Ltd.) was used for filtration, and the solution was degreased, and the obtained filtrate was washed with 50 ml of isopropyl alcohol, and then filtered. The resulting filtrate was dried in a vacuum oven at 50 °C.

(Example 7) (B-6) 4,4'-isophorone double (half-calendar)

A solution A in which 22.22 g of isophorone diisocyanate was dissolved in 100 g of ethanol and a solution B in which 25.3 g of a hydrazine was dissolved in 100 g of ethanol were prepared. In a three-necked flask, the solution B was stirred while being controlled at 30 ° C, and the solution A was dropped at a rate of 1.4 g/min. After the completion of the dropwise addition of the solution A, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. Relative to isophorone diisocyanate 1 mole, reacted in such a manner that the hydrazine became 5 moles (mole ratio 1:5).

After completion of the reaction, the ethanol was removed by an evaporator at 50 ° C, and the purified product was measured by a Fourier transform infrared spectrometer. It was confirmed that there was no peak near 3300 cm ^{-1 of} ethanol, and a liquid ruthenium compound was produced.

(Example 8) (A-1) 1,1'-[Methylenebis(cyclohexane-4,1-diyl)]bis[3-(12-aminododedo)urea]

A solution A in which 13.6 g of dicyclohexylmethane-4,4-diisocyanate was dissolved in 79 g of ethanol and 20.7 g of 1,12-diaminododecane (manufactured by TCI) were dissolved in 100 g of ethanol. Liquid B. In a three-necked flask, the solution B was stirred while being controlled at 30 ° C, and the solution A was dropped at a rate of 1.4 g / minute. After the completion of the dropwise addition, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. 1 mol of dicyclohexylmethane-4,4-diisocyanate was reacted in such a manner that 1,12-diaminododecane became 2 mol (mole ratio 1:2).

The reaction liquid was poured into 500 g of water, and the crystallization was promoted. After standing for 1 hour, it was filtered using a filter paper (No. 4, manufactured by Kiriyama Co., Ltd.) in a Kiriyama funnel (manufactured by Kirsan Corporation), and the obtained filtrate was vacuum oven. Drying was carried out at 50 °C. After drying, it was naturally cooled to room temperature, and pulverized by a high-pressure pulverizer (trade name: nano jet mill, manufactured by Aishin Nanotech Co., Ltd.) to produce an amine compound having an average particle diameter (median diameter) of 2.5 μm.

(Example 9) (A-3) 1,1'-[Methylenebis(cyclohexane-4,1-diyl)]bis[3-(6-aminohexyl)urea]

A solution of 12 g of 1,6-diaminohexane (manufactured by TCI) and a solution of 13.6 g of dicyclohexylmethane-4,4'-diisocyanate dissolved in 79 g of ethanol were prepared by dissolving 100 g of ethanol in 100 g of ethanol. B. In a three-necked flask, the solution B was stirred while being controlled at 30 ° C, and the solution A was dropped at a rate of 1.4 g / minute. After the completion of the dropwise addition, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. 1 mol of dicyclohexylmethane-4,4-diisocyanate was reacted in such a manner that 1,6-diaminohexane became 2 mol (mole ratio 1:2).

The solvent was then distilled off under reduced pressure on a rotary evaporator. Natural after drying The mixture was cooled to room temperature, and pulverized by a high-pressure pulverizer (trade name: nano jet mill, manufactured by Aishin Nanotech Co., Ltd.) to prepare an amine compound having an average particle diameter (median diameter) of 2.2 μm.

(Embodiment 10) (A-4) 1,1'-(Hexa-1,6-diyl)bis[3-(12-aminododedo)urea]

A solution A of 49.65 g of 1,12-diaminododecane (manufactured by TCI) and a solution B of 20.54 g of hexamethylene diisocyanate dissolved in 118 g of ethanol were dissolved in 150 g of ethanol. In a three-necked flask, the solution B was stirred while being controlled at 30 ° C, and the solution A was dropped at a rate of 1.4 g / minute. After the completion of the dropwise addition, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. 1 mol of hexamethylene diisocyanate was reacted in such a manner that 1,12-diaminododecane became 2 mol (mole ratio 1:2).

The solvent was then distilled off under reduced pressure on a rotary evaporator. After drying, it was naturally cooled to room temperature, and pulverized by a high-pressure pulverizer (trade name: nano jet mill, manufactured by Aishin Nanotech Co., Ltd.) to produce a diamine urea compound having an average particle diameter (median diameter) of 2.1 μm.

After the completion of the reaction, the filter paper (manufactured by Kiriyama Co., Ltd.) was used for filtration, and the solution was degreased, and the obtained filtrate was washed with 100 ml of ethanol, and then filtered to obtain a filtration. The contents were dried in a vacuum oven at 50 °C.

(Example 11) (A-5) 1,1'-(Hexa-1,6-diyl)bis[3-(2-aminoethyl)urea]

A solution A in which 17.17 g of hexamethylene diisocyanate was dissolved in 118 g of ethanol and a solution B in which 61.36 g of ethylenediamine was dissolved in 150 g of ethanol were prepared. In a three-necked flask, the solution B was controlled and stirred at 25 ° C, and the solution A was dropped at a rate of 1.4 g / minute. After the completion of the dropwise addition of the solution A, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. 1 mol of hexamethylene diisocyanate was reacted in such a manner that ethylene diamine became 10 mol (mole ratio 1:10).

After the completion of the reaction, the filter paper (manufactured by Kiriyama Co., Ltd.) was used for filtration, and the solution was degreased, and the obtained filtrate was washed with 100 ml of ethanol, and then filtered to obtain a filtration. The contents were dried in a vacuum oven at 50 °C. After drying, it is naturally cooled to room temperature and used as a high pressure pulverizer (trade name: nano jet mill, Aishin The product was pulverized by Nanotech Co., Ltd. to produce an amine compound having an average particle diameter (median diameter) of 2.2 μm.

(Embodiment 12) (A-6) 1,1'-(hexane-1,6-diyl)bis[3-(6-aminohexyl)urea]

A solution A in which 17.17 g of hexamethylene diisocyanate was dissolved in 150 g of ethanol and a solution B of 94.9 g of 1,6-diaminohexane (manufactured by TCI) were dissolved in 118 g of ethanol. In a three-necked flask, the solution B was controlled and stirred at 25 ° C, and the solution A was dropped at a rate of 1.4 g / minute. After the completion of the dropwise addition of the solution A, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. 1 mol of hexamethylene diisocyanate was reacted in such a manner that 1,6-diaminohexane became 10 mol (mole ratio 1:10).

The solvent was then distilled off under reduced pressure on a rotary evaporator. After drying, it was naturally cooled to room temperature, and pulverized by a high-pressure pulverizer (trade name: nano jet mill, manufactured by Aishin Nanotech Co., Ltd.) to produce an amine compound having an average particle diameter (median diameter) of 2.3 μm.

(Example 13) (A-2) 1,1'-[Methylenebis(cyclohexane-4,1-diyl)]bis[3-(2-aminoethyl)urea]

A solution A in which 13.55 g of dicyclohexylmethane 4,4'-diisocyanate was dissolved in 100 g of ethanol and a solution B of 15.5 g of ethylenediamine (manufactured by TCI) were dissolved in 79 g of ethanol. In a three-necked flask, the solution B was controlled and stirred at 25 ° C, and the solution A was dropped at a rate of 1.4 g / minute. After the completion of the dropwise addition of the solution A, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. 1 mol of hexamethylene diisocyanate was reacted in such a manner that 1,6-diaminohexane became 5 mol (mole ratio 1:5).

After the completion of the reaction, the filter paper (manufactured by Kiriyama Co., Ltd.) was used for filtration, and the solution was degreased, and the obtained filtrate was washed with 100 ml of ethanol, and then filtered to obtain a filtration. The contents were dried in a vacuum oven at 50 °C. After drying, it was naturally cooled to room temperature, and pulverized by a high-pressure pulverizer (trade name: nano jet mill, manufactured by Aishin Nanotech Co., Ltd.) to produce an amine compound having an average particle diameter (median diameter) of 2.2 μm.

(synthesis example) (A-5') 1,1'-(hexane-1,6-diyl)bis[3-(2-aminoethyl)urea]

Ethylenediamine 61.36g (1020mmol) and toluene 150g A three-necked flask was stirred, and a solution of 17.17 g (102 mmol) of toluene (118.5 g (150 ml)) of hexamethylene diisocyanate was dropped. The reaction time was controlled to 30 minutes, and the reaction liquid was 40 °C. After the completion of the dropwise addition, the reaction liquid was filtered, and the precipitate was washed with toluene, and then poured into water. After stirring for 1 hour, filtration was carried out, and the obtained filtrate was concentrated under reduced pressure with an evaporator to confirm a precipitate. The reacted hexamethylene diisocyanate and ethylenediamine were 1 mol relative to hexamethylene diisocyanate and 10 mol of ethylene diamine (1:10 molar ratio). The obtained precipitate was washed with ethanol (EtOH), and dried under reduced pressure, and the obtained crystal was pulverized by a high-pressure pulverizer (trade name: nano jet mill, manufactured by Aishin Nanotech Co., Ltd.) to prepare an average particle diameter (median position). Amine compound of 2.1 μm in diameter.

(Example 14) (A-7) N,N'-hexamethylene[carbonylbis(ureidodiyl)(2-aminoethyl)]-[carbonylbis(ureidodiyl)(6-aminohexyl)]

Into 240 g of isopropyl alcohol, 18.3 g of a solution A of hexamethylene diisocyanate (manufactured by TCI Co., Ltd.) and 33.48 g of 1,6-hexanediamine and ethylenediamine were dissolved in 72.6 g of isopropyl alcohol. 18.3 g of solution B. In a three-necked flask, the solution B was controlled and stirred at 25 ° C, and the solution A was dropped at a rate of 1.4 g / minute. After the completion of the dropwise addition of the solution A, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. 1 mol of hexamethylene diisocyanate was reacted in such a manner that ethylene diamine became 5 mol and 1,6-diaminohexane became 5 mol (molar ratio 1:5:5).

After the completion of the reaction, the filter paper (manufactured by Kiriyama Co., Ltd.) was used for filtration, and the solution was degreased, and the obtained filtrate was washed with 100 ml of isopropyl alcohol, and then filtered. The filtrate was dried in a vacuum oven at 50 °C. After drying, it was naturally cooled to room temperature, and pulverized by a high-pressure pulverizer (trade name: nano jet mill, manufactured by Aishin Nanotech Co., Ltd.) to produce an amine compound having an average particle diameter (median diameter) of 2.2 μm.

[Manufacture of epoxy resin]

A partially esterified epoxy resin is produced according to the production method described in JP-A-H05-295087. Specifically, a partially esterified epoxy resin (partially methacrylated epoxy resin) was produced as follows.

(A) High-purity bisphenol A type epoxy resin: 1000 parts by mass of EPICLON-850S (manufactured by DIC Corporation), 250 parts by mass of methacrylic acid, 900 parts by mass of toluene, and 2 parts by mass of triethylamine. Methoxy Phenol: 2 parts by mass, heated and stirred at 90 ° C for 8 hours to obtain a partial addition reaction product.

(B) Toluene: 4500 parts by mass of the product of the above (A), a diluted solution, and after adding pure water: 4500 parts by mass, the mixture was stirred at room temperature for 1 hour, and then allowed to stand to separate the aqueous layer. Remove. Repeat the washing operation 3 to 5 times, then wash the same amount of 1N NaOH solution 3 to 5 times, and repeat only 3 to 5 times with the same amount of pure water, use the final washing water. The ion conductivity of the ion conductivity measuring instrument (manufactured by Horiba, Ltd.: conductivity meter) was measured and found to be 10 μS/cm or less.

(C) The solution obtained by filtering the solution of the above (B) was concentrated at 70 ° C under reduced pressure, and toluene was completely removed and purified to synthesize a partially methacrylated epoxy resin.

Further, according to the above synthesis example, a partially acrylated epoxy resin was synthesized in the same manner using acrylic acid instead of methacrylic acid.

[Manufacture of Liquid Crystal Sealant Composition]

100 parts by mass of the above-mentioned partially methacrylated epoxy resin, 15 parts by mass of spherical cerium oxide (SO-C1, manufactured by ADMAFINE Co., Ltd.) as an inorganic filler, and F-351 (manufactured by Zeon Corporation, Japan) as an organic filler 15 parts by mass, 3 parts by mass of IRGACURE 907 (manufactured by BASF Japan Co., Ltd.) as a photoradical initiator, 2 parts by mass of KBM-403 (manufactured by Shin-Etsu Chemical Co., Ltd.) as a decane coupling agent, and Example 1 as a curing agent 5, 8~12, 14 hardener, 1 equivalent of epoxy equivalent of 1 part of the above methacrylated epoxy resin, with THREE- ONE MOTOR (manufactured by IKA Corporation, trade name; RW28 basic) was uniformly dispersed to obtain a liquid crystal sealant resin composition.

Commercially available decanediodecanoate (DDH, manufactured by Otsuka Chemical Co., Ltd.) was used as Comparative Example 1, and commercially available 1,3-bis(decylcarboethyl)-5-isopropyl was used as Comparative Example 2. A liquid crystal sealant composition was produced in the same manner as described above except for the carbamide (AJICUREVDH, manufactured by Ajinomoto Fine-Techno Co., Inc.).

[Method of measuring the strength of the next step]

Fig. 2 is a view for explaining a method of measuring the bonding strength using the liquid crystal sealing agent compositions of Examples 1 to 5, 8 to 12, and 14 and Comparative Examples 1 and 2. As shown in Fig. 2, ITO glass 8 having a thickness of 0.5 mm and 3.0 cm (the ITO electrode film on the glass surface) and a glass 9 having a thickness of 0.5 mm and 2.3 cm were prepared. The liquid crystal sealant composition 2 was applied to the center line of the ITO glass from 9 mm at both ends, and the thickness was 1.5 to 2.0 mm and the thickness was 6.0 to 10.0 μm as the adhesion surface, and the 3.0 cm square ITO glass 8 and 2.3 cm were applied. One side of the square glass 9 is overlapped, and the two are bonded to each other to form the test piece 10. The bonded test piece 10 was irradiated with UV 3000 mJ (trade name: UB-031-A/BM-E1, manufactured by iGrafx Co., Ltd.), and then heated at 120 ° C for 60 minutes to cure the liquid crystal sealant composition 2. The point of 5 mm of the center line end of the ITO glass 8 of the test piece 10 after the hardening was pulled away by a universal material testing machine (manufactured by Shimadzu Corporation; AGS), and the subsequent strength was measured. The results are shown in Table 1.

[attachment of glass bonding strength to film]

A rubbing-treated alignment film (Sang Aibo SE-7492, manufactured by Nissan Chemical Industries Co., Ltd.) having a thickness of 0.7 mm and a size of 3.0 cm was prepared (glass film having an alignment film) and a thickness of 0.7 mm, 2.3 cm square, and glass 8 The treated alignment film glass 9 was also treated. As shown in Fig. 2, the liquid crystal sealant composition 2 was applied to the center line of the glass at a distance of 9 mm from both ends as a bonding surface to have a diameter of 1.5 mm to 2.0 mm and a thickness of 6.0 μm to 10.0 μm, and a 3.0 cm square was combined. The alignment film glass 8 and one side of the 2.3 cm square alignment film glass 9 were bonded together to form the test piece 10. The test piece 10 to be bonded was irradiated with UV 3000 mJ (trade name: UB-031-A/BM-E1, manufactured by iGrafx Co., Ltd.), and then heated at 120 ° C for 60 minutes to cure the liquid crystal sealant composition 2. The point of 5 mm at the end of the center line of the ITO glass 8 of the test piece 10 after the hardening was pulled away by a universal material testing machine (manufactured by Shimadzu Corporation; AGS), and the bonding strength was measured.

[Orientation test method]

A liquid crystal sealant composition of Example 11 (hardener: A-5) and Comparative Example 1 (hardener: DDH) was used, and a sealing dispenser was used to have a cross-sectional area of 4000 μm ² in a rubbing-treated alignment film. (ITO, SE-7492, manufactured by Nissan Chemical Industries Co., Ltd.) was dispensed on an ITO glass substrate (60 mm × 70 mm × 0.7 mmt). After that, liquid crystal (TN liquid crystal, MLC-11900-080, manufactured by Merck) was dropped on the substrate, and the upper and lower substrates were bonded by a liquid crystal dropping method (ODF method) and irradiated with ultraviolet rays (UV irradiation device: UVX-01224S1, Ushio motor) Company system, illuminance and irradiation time: 50mJ, 50mW/cm ² /365nm for 1 second, 200mJ, 50mW/cm ² /365nm for 4 seconds) Hardening, then heat in a hot air oven at 120 °C for 1 hour Hardening, the test cell for the alignment test was prepared. In the case where the illuminance was 0 mJ, the liquid crystal and the sealant were not irradiated with ultraviolet rays after the bonding, and the film was thermally cured in a hot air oven at 120 ° C for 1 hour to prepare a test cell for the alignment test.

When the obtained panel is sealed, the liquid crystal alignment state is indeed recognize. It was confirmed by an optical microscope that the polarizing plate was sandwiched between the test cells in the state of the crossed polarizer, and the observation was carried out. The alignment state of the corner portion and the straight portion of the liquid crystal in the illuminance of 200 mJ and 50 mJ was observed. The evaluation criteria of the liquid crystal alignment are judged by the presence or absence of alignment disorder at the time of sealing. In the case of sealing, the alignment disorder is "○" when it is 50 μm or less, and "X" when there is more than one alignment disorder. The results are shown in Table 2.

The hardener of the present invention was used as shown in Table 1 (Example 1) The liquid crystal sealant composition of ~5, 8 to 12, and 14) has a higher bonding strength than the use of the curing agents of Comparative Examples 1 and 2 when the glass and the ITO glass are bonded to each other. Further, the alignment property of the alignment film of the liquid crystal sealing agent composition of Example 11 (hardener A-5) was 50 μm or less at the illuminance of 50 mJ and 200 mJ, which was in a good state, but the use of Comparative Example 1 was used. The alignment of the alignment film is more than 50 μm when the illuminance is 50 mJ and 200 mJ. From the results, it was confirmed that the curing agent of the present invention, the resin composition using the same, and the liquid crystal sealing agent composition satisfy the diversification and the versatility required for the sealing agent to be used in the liquid crystal display panel or the like, and at the same time, the performance The adhesion strength at the time of cutting out of the unit cell and the peeling of the IC for driving the liquid crystal cell are suppressed.

(Example 15)

A solution A in which 17.17 g of hexamethylene diisocyanate was dissolved in 118 g of ethanol and a solution B in which 61.36 g of ethylenediamine was dissolved in 150 g of ethanol were prepared. In a three-necked flask, the solution B was controlled and stirred at 25 ° C, and the solution A was dropped at a rate of 1.4 g / minute. After the completion of the dropwise addition of the solution A, the reaction liquid was measured by a Fourier transform infrared spectrometer, and it was confirmed that no peak near 2250 cm ^-1 from the isocyanate group was completed. 1 mol of hexamethylene diisocyanate was reacted in such a manner that ethylene diamine became 10 mol (mole ratio 1:10).

After the completion of the reaction, the filter paper (manufactured by Kiriyama Co., Ltd.) was used for filtration, and the solution was degreased, and the obtained filtrate was washed with 100 ml of ethanol, and then filtered to obtain a filtration. The contents were dried in a vacuum oven at 50 °C. After drying, it was naturally cooled to room temperature, and pulverized by a high-pressure pulverizer (trade name: nano jet mill, manufactured by Aishin Nanotech Co., Ltd.) to produce an amine compound (A-5) having an average particle diameter (median diameter) of 2.2 μm. .

10 g of the above-obtained amine compound (A-5) and Liu Ya 1.36 g of methyl diisocyanate was mixed in 80 ml of methylcyclohexane, and subjected to constant temperature treatment at 50 ° C for 24 hours.

After that, the treatment liquid was filtered using a filter paper (No. 4, manufactured by Kiriyama Co., Ltd.), and filtered by a Kiriyama funnel (manufactured by Kiriyama Co., Ltd.) to carry out deliquoring. The obtained filtrate was mixed in 100 ml of methylcyclohexane, and the filtration operation was repeated three times in the same manner as described above. The final filter was dried in a vacuum dryer (manufactured by ESPEC Co., Ltd.) at 50 ° C for 1 hour at 1 Torr to obtain a curing agent (E-1) containing a compound treated with an isocyanate compound as an amine compound.

10 g of the above-obtained amine compound (A-5) and Liu Ya 1.35 g of methyl diisocyanate and 1.255 g of hydrogenated bisphenol A type epoxy resin (YX8034, manufactured by JER Co., Ltd.) were mixed in 80 ml of toluene, and subjected to constant temperature treatment at 50 ° C for 24 hours.

After that, the treatment liquid was made of filter paper (No. 4, manufactured by Kiriyama Co., Ltd.). The Kiriyama funnel (manufactured by Kiriyama Co., Ltd.) was filtered and dehydrated. The obtained filtrate was mixed in 100 ml of toluene, and the filtration operation was repeated three times in the same manner as described above. The final filter was dried in a vacuum dryer (manufactured by ESPEC) at 50 ° C for 1 hour at 1 Torr to obtain a curing agent (E-2) containing a compound of an amine compound treated with an isocyanate compound and an epoxy resin.

[Manufacture of Liquid Crystal Sealant Composition]

100 parts by mass of the above-mentioned partially methacrylated epoxy resin, 15 parts by mass of spherical cerium oxide (SO-C1 manufactured by ADMAFINE Co., Ltd.) as an inorganic filler, and F-351 as an organic filler (Japanese Zeon) 15 parts by mass of IRGACURE 907 (manufactured by BASF Japan Co., Ltd.) as a photoradical initiator, and 2 parts by mass of KBM-403 (manufactured by Shin-Etsu Chemical Co., Ltd.) as a decane coupling agent, E as a curing agent -1 or E-2, which is uniformly dispersed with THREE-ONE MOTOR (manufactured by IKA Co., Ltd., trade name; RW28 basic) in an amount of 15 parts by mass based on 100 parts by mass of the above-mentioned partially methacrylated epoxy resin, and a liquid crystal sealant resin composition is obtained. Things.

[assessment] (Stability test) Liquid stability

The initial viscosity of the liquid crystal sealant composition obtained as described above was measured (within 2 hours). Further, the viscosity at 25 ° C and 2 weeks was measured, and the viscosity change rate after 2 weeks was calculated based on the initial viscosity (%). /2weeks).

Further, the viscosity was measured as follows. A RE-105U viscometer (manufactured by Toki Sangyo Co., Ltd.) was installed with a 3°×R7.7 conical rotor, and 0.15 ml of the liquid crystal sealant composition was placed in a conical rotor, and a liquid crystal of 25° C. was measured at 2.5 rpm. The viscosity of the sealant composition. When it is outside the measurement range, it cannot be measured. Further, the outside of the measurement range was 1,200,000 mPa·s.

Warming fluid stability

The initial viscosity of the liquid crystal sealing agent composition obtained above was measured, and the viscosity after 40 hours and 22 hours was measured, and the rate of change of viscosity (%/22 hrs) after heating for 22 hours was calculated based on the initial viscosity.

The results of liquid stability and warming fluid stability are shown in Table 3.

It can be understood from the results in Table 3 that the addition of the amine compound is different. The isocyanate addition amine compound of cyanate ester is remarkably liquid stable, and the rate of change of the stability of the heating liquid is small, and in particular, the rate of change of the stability of the heating liquid is small.

(hardening test)

The liquid crystal sealant composition (resin composition) obtained above Table the following two conditions described the 4 (only 120 ℃ 1 hour and UV3000mJ / cm ² 120 ℃ 1 hour after treatment) be hardened, the hardened obtained The sheet was measured by FT-IR and evaluated for hardenability. The epoxy resin hardening rate calculation method uses the following formula. Further, the methacryl radical hardening rate was calculated by substituting the peak of the epoxy group in the following formula to the peak of the methacryl group.

Reference peak; 1540~1480cm ^-1 (near peak of 1510cm ^-1 )

Epoxy group peak; 925 ~ 895cm ^-1 (peak wave near 910cm ^-1)

Peak of methacrylic group; 1650~1625cm ^-1 (near peak of 1635cm ^-1 )

As a result of Table 4, there was no significant decrease in hardenability even when the isocyanate treatment was carried out. That is, even if it is treated with isocyanate, the liquid stability can be improved without lowering the hardenability.

[industrial use]

According to the present invention, it is possible to obtain a diversification of the adhesion of the thinning and dissimilar materials, and it is possible to sufficiently suppress the peeling of the cell during the cutting of the cell and the mounting of the IC for driving the liquid crystal cell. The hardening agent of the strength, the resin composition of the present invention, the resin composition using the same, and the liquid crystal sealing agent composition can be applied to a sealant or a sealant of an electronic component such as a liquid crystal display panel, and have industrial applicability.

The contents of Japanese Patent Application No. 2012-155976 are incorporated herein by reference in its entirety.

All documents, patent applications, and technical specifications described in the specification are incorporated herein by reference.

Claims (14)

An epoxy resin and/or a hardener for a resin having at least one unsaturated bond in a molecule, characterized by having an isocyanate compound and a hydrazine or having two or more amine groups in the molecule A compound having at least one first-order amine group in the molecule obtained by the reaction of the valence amine compound. An epoxy resin and/or a hardener for a resin having at least one unsaturated bond in a molecule, characterized by containing the following formula (I) Wherein R ¹ is a single bond, or a C ₁ -C ₁₂ alkyl group, a C ₂ -C ₁₂ alkyl group interrupted discontinuously by one or more NH or O atoms (bonded to a N atom) The H atom may be substituted by an amine group or a C ₁ -C ₁₂ alkylamine group), a C ₃ -C ₁₂ cycloalkyl group, a C ₁ -C ₁₂ alkyl group-C ₃ -C ₁₂ cycloalkane Base, C ₁ ~ C ₁₂ alkyl-C ₃ ~ C ₁₂ cycloalkyl-C ₁ ~ C ₁₂ alkyl, C ₃ ~ C ₁₂ cycloalkyl - C ₁ ~ C ₁₂ alkyl - C ₃ ~ C ₁₂ cycloalkyl, C ₆ ~ C ₁₄ extended aryl, C ₁ ~ C ₄ alkyl - C ₆ ~ C ₁₄ extended aryl, C ₁ ~ C ₄ alkyl - C ₆ ~ C ₁₄ an arylene group -C ₁ ~ C ₄ alkylene, or C ₆ ~ C ₁₄ arylene group -C ₁ ~ C ₄ alkylene -C ₆ ~ C ₁₄ arylene group (here, a straight-chain alkylene Or a branched chain and may be substituted by halogen, C ₃ ~ C ₁₂ cycloalkyl or C ₆ - C ₁₄ extended aryl is unsubstituted, or substituted by halogen or C ₁ - C ₄ alkyl), n is 1, 2 When 3 or 4, n is 2 or more, R ^{1 is} independent of each other, and when n is 1, A is a C ₁ - C ₁₂ alkyl group, and C is discontinuously interrupted by one or more O atoms. ₂ to C ₁₂ alkyl, C ₂ -C ₁₂ alkyloxycarbonylalkylene, C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl- C ₃ ~C ₁₂ cycloalkyl, C ₃ -C ₁₂ cycloalkyl-C ₁ ~C ₁₂ alkyl -C ₃ ~C ₁₂ cycloalkyl, C ₆ ~C ₁₄ aryl, C ₁ ~C _4- alkyl-C ₆ -C ₁₄ aryl, C ₆ -C ₁₄ aryl-C ₁ ~C ₄ alkyl -C ₆ -C ₁₄ extended aryl (here, alkyl is straight or branched) a chain which may be substituted by halogen, a C ₃ -C ₁₂ cycloalkyl group, a C ₃ -C ₁₂ cycloalkylene group, a C ₆ -C ₁₄ aryl group, or a C ₆ -C ₁₄ aryl group which is unsubstituted or halogen or When C ₁ to C ₄ alkyl group is substituted or (meth) propylene fluorenyloxyalkyl group, and n is 2, A is a C ₁ - C ₁₂ alkyl group, and one or more O atoms are used. Non-continuously interrupted C ₂ -C ₁₂ alkylene, C ₁ -C ₁₂ alkyloxycarbonylalkylene, C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl -C ₃ ~ C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl-C ₃ ~C ₁₂ cycloalkyl-C ₁ -C ₁₂ alkyl, C ₃ ~C ₁₂ cycloalkyl-C ₁ ~C ₁₂ alkylene -C ₃ ~ C ₁₂ cycloalkyl alkylene, di-C ₃ ~ C ₁₂ cycloalkane-diyl group, C ₆ ~ C ₁₄ arylene group, C ₁ ~ C ₄ alkylene -C ₆ ~ C ₁₄ arylene a radical -C ₁ -C ₄ alkylene group, or a C ₆ -C ₁₄ aryl group -C ₁ -C ₄ alkylene group -C ₆ -C ₁₄ aryl group (here, the alkyl group is a straight chain or a branch Chain and can Halogen substituted, C ₃ ~ C ₁₂ cycloalkyl, C ₆ ~ C ₁₄ extended aryl is unsubstituted, or substituted by halogen or C ₁ ~ C ₄ alkyl), where n is 3, A is lower Description (1) (wherein R ^{2 is the} same or different and is a C ₁ to C ₁₂ alkyl group of a straight or branched chain), and the following formula (2) (wherein R ^{3 is the} same or different and is a C ₁ to C ₁₂ alkyl group of a straight or branched chain) or the following formula (3) (wherein R ^{4 is the} same or different and is a C ₁ to C ₁₂ alkyl group of a straight or branched chain, and R ⁵ is CH), and when n is 4, A is a formula (4) below. Wherein X ³ is Si, or C ₃ -C ₁₂ cycloalkyl-C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl, or C ₆ -C ₁₄ aryl-C ₁ -C _4- alkyl-C ₆ -C ₁₄ aryl (here, the alkyl group is a straight or branched chain, which may be substituted by 1 to 6 halogens, C ₃ to C ₁₂ cycloalkyl or C ₆ to C ₁₄ The aryl group is a compound having at least one first-order amine group in the molecule represented by a tetravalent residue derived from a halogen group or a C ₁ -C ₄ alkyl group. The hardener according to claim 2, wherein the compound having at least one first-order amine group in the molecule is the following formula (Ia) Wherein R ^{1 is} independent of each other, and is synonymous with claim 2; X ¹ is a C ₁ -C ₁₂ alkyl group, and C ₂ -C ₁₂ alkyl group interrupted discontinuously by one or more O atoms, C ₁ ~ C ₁₂ alkyloxycarbonylalkyl, C ₃ ~ C ₁₂ cycloalkyl, C ₁ ~ C ₁₂ alkyl - C ₃ ~ C ₁₂ cycloalkyl, C ₁ ~ C ₁₂ alkyl -C ₃ ~ C ₁₂ cycloalkyl alkylene -C ₁ ~ C ₁₂ alkylene, C ₃ ~ C ₁₂ cycloalkyl alkylene -C ₁ ~ C ₁₂ alkylene -C ₃ ~ C ₁₂ cycloalkyl alkylene , C ₃ ~ C ₁₂ cycloalkane diyl, C ₆ ~ C ₁₄ extended aryl, C ₁ ~ C ₄ alkyl - C ₆ ~ C ₁₄ extended aryl - C ₁ ~ C ₄ alkyl, or C ₆ ~ C ₁₄ aryl-C ₁ ~ C ₄ alkyl - C ₆ ~ C ₁₄ extended aryl (here, alkyl is linear or branched and can be substituted by halogen, C ₃ ~ C ₁₂ ring extension The alkyl or C ₆ -C ₁₄ extended aryl group is unsubstituted or substituted by halogen or C ₁ -C ₄ alkyl). The hardener according to claim 2, wherein the compound having at least one first-order amine group in the molecule is the following formula (IIa) Wherein R ^{1 is the} same as the claim 2, X ² is a C ₁ -C ₁₂ alkyl group, and C ₂ -C ₁₂ alkyl, C ₁ -C ₁₂ alkane is discontinuously interrupted by one or more O atoms. Alkyloxycarbonylalkylene, C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ alkyl-C ₃ -C ₁₂ cycloalkyl, C ₃ -C ₁₂ cycloalkyl-C ₁ ~C ₁₂ Alkyl-C ₃ -C ₁₂ cycloalkylene, C ₆ -C ₁₄ aryl, C ₁ -C ₄ alkyl-C ₆ -C ₁₄ aryl, C ₆ -C ₁₄ aryl-C ₁ ~C ₄ alkyl-C ₆ ~ C ₁₄ extended aryl (here, alkyl is linear or branched and can be substituted by halogen, C ₃ ~ C ₁₂ cycloalkyl, C ₃ ~ C ₁₂ cycloalkyl, The C ₆ -C ₁₄ aryl group or the C ₆ -C ₁₄ aryl group is unsubstituted or substituted by halogen or C ₁ -C ₄ alkyl group), or (meth) propylene decyloxyalkyl group. The curing agent according to any one of claims 1 to 4, further comprising a compound obtained by treating a compound having at least one first-order amine group in the molecule with an isocyanate compound. The curing agent according to any one of claims 1 to 4, further comprising a compound obtained by treating a compound having at least one first-order amine group in the molecule with an isocyanate compound and an epoxy resin. The curing agent according to any one of claims 1 to 4, further comprising a compound obtained by treating a compound having at least one first-order amine group in the molecule with an isocyanate compound and a compound having a hydroxyl group. A resin composition comprising the curing agent (A) according to any one of claims 1 to 7, and an epoxy resin and/or a resin (B) having at least one unsaturated bond. The resin composition according to claim 8, wherein the epoxy resin is a partially esterified epoxy resin obtained by reacting 1 equivalent of an epoxy group with 10 to 90 equivalent % of (meth)acrylic acid. The resin composition according to claim 8 or 9, wherein the epoxy group has 1 equivalent of the epoxy group and the total amount of the first-stage amine group contained in the curing agent (A) is 0.001 to 10 equivalents. The resin composition according to any one of claims 8 to 10, wherein a total of 1 equivalent of the epoxy group of the epoxy resin and 1 equivalent of the unsaturated bond of the resin having at least one unsaturated bond in the molecule The total amount of the first-stage amine groups contained in the hardener (A) is 0.001 to 10 equivalents. A liquid crystal sealant composition comprising the resin composition according to any one of claims 8 to 11. A liquid crystal display panel, the characteristics of which are described in claim 12 The liquid crystal sealant composition is obtained. A method for producing a liquid crystal display panel characterized in that, in the liquid crystal dropping method, the liquid crystal sealant composition described in claim 12 is used, and photohardening is performed, followed by thermal curing.