Additives, plasticizers, curable compositions, adhesives, cured products, and pressure-sensitive adhesives

Abstract

A compound according to the present invention is represented by general formula (1).　General formula (1): (In formula (1), A represents an n-valent organic group that contains a sulfur atom; n represents an integer of 3 or more; S represents a sulfur atom; each X represents a single bond or a carbonyl group; the X moieties may be the same as or different from each other; each R represents an aliphatic hydrocarbon group, an aromatic hydrocarbon group or an aromatic aliphatic hydrocarbon group; and the R moieties may be the same as or different from each other.)

Description

[Technical Field]

[0001] The present invention relates to a compound, an additive, a plasticizer, a curable composition, an adhesive, a cured product, and a pressure-sensitive adhesive. [Background technology]

[0002] Optical resins used as adhesives and pressure sensitive adhesives in various optical fields have a relatively high refractive index.

[0003] Optical resins may be required to be flexible depending on their applications. Therefore, the addition of a plasticizer to optical resins has been considered. For example, dioctyl phthalate (DOP) is known as a plasticizer. Another known plasticizer is 2-mercaptoethyl sulfide dibenzoate (see, for example, Patent Document 1 (Example 11)). [Prior art documents] [Patent documents]

[0004] [Patent Document 1] Japanese Patent Application Publication No. 61-019654 Summary of the Invention [Problem to be solved by the invention]

[0005] When the above-mentioned plasticizer is added to an optical resin, the crystallinity of the optical resin is reduced and the flexibility is improved. However, the reduction in the crystallinity of the optical resin may reduce the refractive index of the optical resin. Furthermore, for example, if the refractive index of the optical resin is not reduced by the plasticizer, the crystallinity of the optical resin may not be reduced sufficiently, and the flexibility may not be improved.

[0006] The present invention relates to a compound, an additive, a plasticizer, a curable composition, an adhesive, a cured product, and a pressure-sensitive adhesive for obtaining a cured product that has both a refractive index and flexibility. [Means for solving the problem]

[0007] The present invention [1] includes a compound represented by the following general formula (1): General formula (1);

[0008] [ka] (In formula (1), A represents an n-valent organic group containing a sulfur atom. n represents an integer of 3 or greater. S represents a sulfur atom. X represents a single bond or a carbonyl group. X may be the same or different. R represents an aliphatic hydrocarbon group, an aromatic hydrocarbon group, or an araliphatic hydrocarbon group. R may be the same or different.)

[0009] The present invention [2] includes the compound according to the above [1], wherein A represents an organic group containing a sulfur atom and a main group element atom (excluding sulfur and hydrogen atoms), and the ratio of the number of sulfur atoms to the total number of sulfur atoms and the main group element atoms (excluding sulfur and hydrogen atoms) in A exceeds 20%.

[0010] The present invention [3] includes the compound according to the above [1] or [2], which is represented by the following general formula (2) or the following general formula (3). General formula (2);

[0011] [ka] (In formula (2), S, X, and R have the same meanings as S, X, and R in formula (1). In formula (2), the portion surrounded by a dashed line represents the organic group A (n=3) in formula (1).) General formula (3);

[0012] [ka] (In formula (3), S, X, and R have the same meanings as S, X, and R in formula (1). In formula (3), the portion surrounded by a dashed line represents the organic group A (n=4) in formula (1).)

[0013] The present invention [4] includes the compound according to any one of the above [1] to [3], wherein R represents a methyl group, a phenyl group, or a benzyl group.

[0014] The present invention [5] includes the compound according to any one of the above [1] to [3], in which X represents a carbonyl group and R represents an aromatic aliphatic hydrocarbon group.

[0015] The present invention [6] includes an additive containing the compound according to any one of the above [1] to [5].

[0016] The present invention [7] includes a plasticizer containing the compound according to any one of the above [1] to [5].

[0017] The present invention [8] includes a curable composition containing the plasticizer described in [7] above and a curable compound.

[0018] The present invention [9] further comprises an ultraviolet absorber, a light-resistant stabilizer, Agent and at least one additive selected from the group consisting of an antioxidant, and the ratio of the additive is 10×10 -6 Mass part or more 10000×10 -6 The curable composition according to the above item [8] is contained in an amount of not more than parts by mass.

[0019] The present invention

[10] includes an adhesive comprising the curable composition according to the above [8] or [9].

[0020] The present invention

[11] includes a cured product containing the plasticizer described in [7] above and a cured resin.

[0021] The present invention

[12] includes the cured product according to the above

[11] , which has a refractive index of 1.60 or more and a tensile storage modulus at 25°C of 100 MPa or less.

[0022] The present invention

[13] further comprises an ultraviolet absorber, a light-resistant stabilizer, Agent and at least one additive selected from the group consisting of antioxidants, and the ratio of the additive to 1 part by mass of the cured product is 10 × 10 -6 Mass part or more 10000×10 -6 The cured product according to

[11] or

[12] is contained in an amount of not more than parts by mass.

[0023] The present invention

[14] includes the cured product according to any one of the above

[11] to

[13] , wherein the cured resin includes a reaction product of a base agent containing an acrylic polyol and a curing agent containing a polyisocyanate.

[0024] The present invention

[15] includes the cured product according to any one of the above

[11] to

[13] , wherein the cured resin includes a cured acrylic resin.

[0025] The present invention

[16] includes a pressure-sensitive adhesive containing the cured product according to any one of the above

[11] to

[15] . [Effects of the Invention]

[0026] The compound, additive, plasticizer, curable composition, and adhesive of the present invention can provide a cured product that has both a refractive index and flexibility.

[0027] The cured product and adhesive of the present invention contain the above compound and therefore have both a refractive index and flexibility. DETAILED DESCRIPTION OF THE INVENTION

[0028] 1.Compound (1) Compound structure The compound of the present invention is represented by the following general formula (1). General formula (1);

[0029] [ka] (In formula (1), A represents an n-valent organic group containing a sulfur atom. n represents an integer of 3 or greater. S represents a sulfur atom. X represents a single bond or a carbonyl group. X may be the same or different. R represents an aliphatic hydrocarbon group, an aromatic hydrocarbon group, or an araliphatic hydrocarbon group. R may be the same or different.)

[0030] (2) A in the formula In the above formula (1), A represents an n-valent organic group containing a sulfur atom. Preferably, A represents an organic group containing a sulfur atom and a main group atom (excluding sulfur and hydrogen atoms).

[0031] In the typical element atoms (excluding sulfur and hydrogen atoms), typical elements (excluding sulfur and hydrogen) refer to elements with atomic numbers of 2 to 15, elements with atomic numbers of 17 to 20, elements with atomic numbers of 31 to 38, elements with atomic numbers of 49 to 56, and elements with atomic numbers of 81 to 88. Preferred typical elements (excluding sulfur and hydrogen) include elements with atomic numbers of 2 to 15, more preferably elements with atomic numbers of 6 to 9, and more specifically, carbon, nitrogen, oxygen, and fluorine. These may be used alone or in combination of two or more types.

[0032] More preferably, the typical elements (excluding sulfur and hydrogen) are carbon and oxygen, and particularly preferably carbon. From the viewpoint of achieving a good balance between refractive index and flexibility, A more preferably represents an organic group containing a sulfur atom and a carbon atom, and even more preferably represents an organic group consisting of a sulfur atom and a carbon atom.

[0033] n is the valence of A. n is an integer of 3 or more. n is preferably an integer of 3 or more and 8 or less. n is more preferably an integer of 3 or more and 6 or less. n is even more preferably 3 or 4.

[0034] Examples of n-valent A include residues of n-functional thiols. More specifically, A includes residues obtained by removing mercapto groups from trifunctional or higher functional sulfur-containing polythiols (hereinafter referred to as trifunctional or higher functional sulfur-containing polythiol residues).

[0035] A tri- or higher functional sulfur-containing polythiol is an organic compound containing three or more mercapto groups in one molecule and one or more (preferably two or three) sulfur atoms other than the mercapto groups. Examples of tri- or higher functional sulfur-containing polythiols include sulfur-containing trithiol, sulfur-containing tetrathiol, sulfur-containing pentathiol, sulfur-containing hexathiol, and sulfur-containing octathiol.

[0036] Sulfur-containing trithiol is a trifunctional thiol containing a sulfur atom in addition to a mercapto group. Examples of sulfur-containing trithiol include 1,2,3-tris(mercaptomethylthio)propane, 1,2,3-tris(2-mercaptoethylthio)propane, 1,2,3-tris(3-mercaptopropylthio)propane, 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane (GST), 2,2-bis(mercaptomethylthio)ethanethiol, 3-mercaptomethylthio-1,7-dimercapto-2,6-dithiaheptane, 3-mercaptomethylthio-1,6-dimercapto-2,5-dithiahexane, 4,6-bis[4-(6-mercaptomethylthio)-1,3-dithianylthio] ]-6-[4-(6-mercaptomethylthio)-1,3-dithianylthio]-1,3-dithiane, tris(mercaptomethylthio)methane, tris(mercaptoethylthio)methane, 2,4,6-tris(mercaptomethylthio)-1,3,5-trithiacyclohexane, tris[(4-mercaptomethyl-2,5-dithiacyclohexyl-1-yl)methylthio]methane, 4-mercaptomethyl-2-(2,3-dimercaptopropylthio)-1,3-dithiacyclopentane, and 4-mercaptomethyl-2-(1,3-dimercapto-2-propylthio)-1,3-dithiacyclopentane.

[0037] The sulfur-containing tetrathiol is a tetrafunctional thiol containing a sulfur atom in addition to a mercapto group. Examples of sulfur-containing tetrathiols include 5,7-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane (FSH), 4,7-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane, 4,8-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane, tetrakis(mercaptomethylthiomethyl)methane, tetrakis(2-mercaptoethylthiomethyl)methane, tetrakis(3-mercaptopropylthiomethyl)methane, bis(2, 3-dimercaptopropyl) sulfide, thiodipropionic acid bis(2,3-dimercaptopropyl ester), dithiodiglycolic acid bis(2,3-dimercaptopropyl ester), thiodipropionic acid bis(2,3-dimercaptopropyl ester), dithiodipropionic acid bis(2,3-dimercaptopropyl ester), 1,1,3,3-tetrakis(mercaptomethylthio)propane, 1,1,2,2-tetrakis(mercaptomethylthio)ethane, 1,1,5,5-tetrakis(mercaptomethylthio)- 3-Thiapentane, 1,1,6,6-tetrakis(mercaptomethylthio)-3,4-dithiahexane, 2,5-bis(4,4-bis(mercaptomethylthio)-2-thiabutyl)-1,4-dithiane, 2,2-bis(mercaptomethylthio)-1,3-propanedithiol, 3,6-bis(mercaptomethylthio)-1,9-dimercapto-2,5,8-trithianonane, 4-[3,5-bis(mercaptomethylthio)-7-mercapto-2,6-dithiaheptylthio]-6-mercaptomethylthio-1,3-dithiane , 1,1-bis[4-(6-mercaptomethylthio)-1,3-dithianylthio]-1,3-bis(mercaptomethylthio)propane, 3-[2-(1,3-dithietanyl)]methyl-7,9-bis(mercaptomethylthio)-1,11-dimercapto-2,4,6,10-tetrathiaundecane, 4-[3,4-bis(mercaptomethylthio)-6-mercapto-2,5-dithiahexylthio]-5-mercaptomethylthio-1,3-dithiolane, 2-[3,4-bis(mercaptomethylthio)-6-mercapto-2,5-dithiahexylthio]mercaptomethylthiomethyl-1,3-dithietane, 4-{1-[2-(1,3-dithietanyl)]-3-mercapto-2-thiapropylthio}-5-[1,2-bis(mercaptomethylthio)-4-mercapto-3-thiabutylthio]-1,3-dithiolane, 1,1,5,5-tetrakis(mercaptomethylthio)-2,4-dithiapentane, and 1,1,3,3-tetrakis(mercaptomethylthio)-2-thiapropane.

[0038] The sulfur-containing pentathiol is a pentafunctional thiol containing a sulfur atom in addition to a mercapto group. Examples of sulfur-containing pentathiols include 1-[4-(6-mercaptomethylthio)-1,3-dithianylthio]-3-[2,2-bis(mercaptomethylthio)ethyl]-7,9-bis(mercaptomethylthio)-2,4,6,10-tetrathiaundecane and bis[4,4-bis(mercaptomethylthio)-1,3-dithiabutyl]-(mercaptomethylthio)methane.

[0039] Sulfur-containing hexathiol is a hexafunctional thiol containing a sulfur atom in addition to a mercapto group. Examples of sulfur-containing hexathiol include 1,1,9,9-tetrakis(mercaptomethylthio)-5-(3,3-bis(mercaptomethylthio)-1-thiapropyl)3,7-dithianonane, tris(2,2-bis(mercaptomethylthio)ethyl)methane, tris(4,4-bis(mercaptomethylthio)-2-thiabutyl)methane, 3,5,9,11-tetrakis(mercaptomethylthio)-1,13-dimercapto-2,6,8,12-tetrathiatridecane, 3,4,8 ...methane, 3,4,8,9-tetrakis(mercaptomethylthio)-5-(3,3-bis(mercaptomethylthio)-1-thiapropyl)methane, 3,4,8,9-tetrakis(mercaptomethylthio)-5-(3,3-bis(mercaptomethylthio)-1-thiapropyl)methane, 3,4,8,9-tetrakis(mercaptomethylthio)-5-(3,3-bis(mercaptomethylthio)-1-thiapropyl) methylthio)-1,11-dimercapto-2,5,7,10-tetrathiaundecane, 4,6-bis[3,5-bis(mercaptomethylthio)-7-mercapto-2,6-dithiaheptylthio]-1,3-dithiane, 3-[2-(1,3-dithietanyl)]methyl-7,9,13,15-tetrakis(mercaptomethylthio)-1,17-dimercapto-2,4,6,10,12,16-hexathiaheptadecane, 4-[3,4,8,9-tetrakis(mercaptomethylthio)-11-mercapto-2,5,7,10 -tetrathiaundecyl]-5-mercaptomethylthio-1,3-dithiolane, 4,5-bis[3,4-bis(mercaptomethylthio)-6-mercapto-2,5-dithiahexylthio]-1,3-dithiolane, 4-[3-bis(mercaptomethylthio)methyl-5,6-bis(mercaptomethylthio)-8-mercapto-2,4,7-trithiaoctyl]-5-mercaptomethylthio-1,3-dithiolane, 2-{bis[3,4-bis(mercaptomethylthio)-6-mercapto-2,5-dithiahexylthio] methyl}-1,3-dithietane, 2-[3,4,8,9-tetrakis(mercaptomethylthio)-11-mercapto-2,5,7,10-tetrathiaundecylthio]mercaptomethylthiomethyl-1,3-dithietane, 2-[3-bis(mercaptomethylthio)methyl-5,6-bis(mercaptomethylthio)-8-mercapto-2,4,7-trithiaoctyl]mercaptomethylthiomethyl-1,3-dithietane, tris[4,4-bis(mercaptomethylthio)-1,3-dithiabutyl]methane, tris[2,2-bis(mercaptomethylthio)-2-thiapropyl]methane, tris[4,4-bis(mercaptomethylthio)-3-thiabutyl]methane, and 2,4,6-tris[3,3-bis(mercaptomethylthio)-2-thiapropyl]-1,3,5-trithiacyclohexane.

[0040] Sulfur-containing octathiols are octafunctional thiols containing sulfur atoms in addition to mercapto groups. Examples of sulfur-containing octathiols include tetrakis(4,4-bis(mercaptomethylthio)-2-thiabutyl)methane, 3,5,9,11,15,17-hexakis(mercaptomethylthio)-1,19-dimercapto-2,6,8,12,14,18-hexathianonadecane, 9-(2,2-bis(mercaptomethylthio)ethyl)-3,5,13,15-tetrakis(mercaptomethylthio)-1,17-dimercapto-2,6,8,10,12,16-hexathiaheptadecane, and tetrakis(2,2 -bis(mercaptomethylthio)ethyl)methane, 3,4,8,9,13,14-hexakis(mercaptomethylthio)-1,16-dimercapto-2,5,7,10,12,15-hexathiahexadecane, 8-[bis(mercaptomethylthio)methyl]-3,4,12,13-tetrakis(mercaptomethylthio)-1,15-dimercapto-2,5,7,9,11,14-hexathiapentadecane, and tetrakis[3,3-bis(mercaptomethylthio)-2-thiapropyl]methane.

[0041] The tri- or higher functional sulfur-containing polythiol residue preferably includes a tri- to hexafunctional sulfur-containing polythiol residue, more preferably a tri- or tetrafunctional sulfur-containing polythiol residue, and even more preferably a trifunctional sulfur-containing polythiol residue.

[0042] That is, in the general formula (1), A is preferably a trifunctional to hexafunctional sulfur-containing polythiol residue, more preferably a trifunctional to tetrafunctional sulfur-containing polythiol residue, and even more preferably a trifunctional sulfur-containing polythiol residue.

[0043] In other words, A is preferably a trivalent to hexavalent organic group containing one or more (preferably two or three) sulfur atoms. A is more preferably a trivalent organic group containing one or more (preferably two or three) sulfur atoms, or a tetravalent organic group containing one or more (preferably two or three) sulfur atoms, and even more preferably a trivalent organic group containing a sulfur atom.

[0044] From the viewpoint of achieving a good balance between refractive index and flexibility, A preferably contains sulfur atoms at a predetermined ratio or more. More specifically, in A, the ratio of the number of sulfur atoms to the total number of sulfur atoms and the number of typical element atoms (excluding sulfur atoms and hydrogen atoms) is, for example, more than 20%, preferably 21% or more, and more preferably 22% or more. Furthermore, from the viewpoint of achieving a good balance between refractive index and flexibility, the ratio of the number of sulfur atoms to the total number of sulfur atoms and the number of typical element atoms (excluding sulfur atoms and hydrogen atoms) is, for example, 80% or less, preferably 50% or less, more preferably 30% or less, and even more preferably 25% or less. The ratio of the number of sulfur atoms to the total number of sulfur atoms and the number of typical element atoms (excluding sulfur atoms and hydrogen atoms) is calculated using the following formula.

[0045] Percentage of sulfur atoms (%) = Number of sulfur atoms / [Number of sulfur atoms + Number of main group atoms (excluding sulfur and hydrogen atoms)] x 100

[0046] The trivalent organic group (organic group A (n=3)) containing one or more sulfur atoms (preferably, two or three, more preferably two) is preferably a residue obtained by removing a mercapto group from the above-mentioned sulfur-containing trithiol, more preferably a residue obtained by removing a mercapto group from 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane (GST) (GST residue).

[0047] The residue (GST residue) obtained by removing the mercapto group from 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane (GST) is represented by, for example, the following general formula (4). General formula (4);

[0048] [ka] (In formula (4), the wavy line indicates the bonding position to the SXR group in formula (1).)

[0049] When A in the above formula (1) is a GST residue, a cured product having both an especially excellent refractive index and especially excellent flexibility can be obtained.

[0050] The GST residue is an organic group consisting of two sulfur atoms and seven carbon atoms. In the GST residue, the ratio of the number of sulfur atoms to the total number of sulfur atoms and main group atoms (excluding sulfur and hydrogen atoms) is approximately 22% (2 / [2 + 7] × 100).

[0051] The tetravalent organic group (organic group A (n=4)) containing one or more sulfur atoms (preferably, two or three, more preferably three) is preferably a residue obtained by removing a mercapto group from the above-mentioned sulfur-containing tetrathiol, more preferably a residue obtained by removing a mercapto group from 5,7-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane (FSH) (FSH residue).

[0052] The residue (FSH residue) obtained by removing the mercapto group from 5,7-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane (FSH) is represented by, for example, the following general formula (5). General formula (5);

[0053] [ka] (In formula (5), the wavy line indicates the bonding position to the SXR group in formula (1).)

[0054] When A in the above formula (1) is an FSH residue, a cured product having both an especially excellent refractive index and especially excellent flexibility can be obtained.

[0055] The FSH residue is an organic group consisting of three sulfur atoms and ten carbon atoms. The ratio of the number of sulfur atoms to the total number of main group atoms (excluding sulfur and hydrogen atoms) in the FSH residue is approximately 23% (3 / [3 + 10] × 100).

[0056] From the viewpoint of refractive index and flexibility, A in the above formula (1) is preferably a GST residue or an FSH residue, more preferably a GST residue.

[0057] (3) S in the equation In the above formula (1), S represents a sulfur atom.

[0058] (4) X in the formula In the above formula (1), X represents a single bond or a carbonyl group.

[0059] When X represents a single bond, S and R in the above formula (1) are directly bonded, that is, when X represents a single bond, the SXR group in the above formula (1) represents an SR group.

[0060] When X represents a carbonyl group, S and R in the above formula (1) are indirectly bonded via the carbonyl group, i.e., when X represents a carbonyl group, the SXR group in the above formula (1) represents an S(C=O)R group.

[0061] The compound of formula (1) has three or more SXR groups depending on the value of n. Each X contained in each SXR group may be the same as or different from each other. Preferably, in formula (1), each X contained in each SXR group is the same as each other.

[0062] R in equation (5) In the above formula (1), R represents an aliphatic hydrocarbon group, an aromatic hydrocarbon group, or an araliphatic hydrocarbon group.

[0063] Examples of the aliphatic hydrocarbon group include aliphatic hydrocarbon groups having 1 to 20 carbon atoms. More specific examples of the aliphatic hydrocarbon group include linear aliphatic hydrocarbon groups having 1 to 20 carbon atoms and cyclic aliphatic hydrocarbon groups having 3 to 20 carbon atoms.

[0064] Examples of the linear aliphatic hydrocarbon group having 1 to 20 carbon atoms include a linear saturated aliphatic hydrocarbon group having 1 to 20 carbon atoms and a linear unsaturated aliphatic hydrocarbon group having 1 to 20 carbon atoms. Examples of the linear saturated aliphatic hydrocarbon group having 1 to 20 carbon atoms include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, a sec-butyl group, a tert-butyl group, a 2-butyl group, a 1-pentyl group, a 2-pentyl group, a 3-pentyl group, a 2-methyl-1-butyl group, an isopentyl group, a tert-pentyl group, a 3-methyl-2-butyl group, a neopentyl group, an n-hexyl group, a 4-methyl-2-butyl group, a 5-methyl-1-butyl group, a 6-methyl-2-butyl group, a 7-methyl-2-butyl group, a 8-methyl-2-butyl group, a 9-methyl-2-butyl group, a 10-methyl-2-butyl group, a 20-methyl-2-butyl group, a 21-methyl-2-butyl group, a 22-methyl-2-butyl group, a 23-methyl-2-butyl group, a 24-methyl-2-butyl group, a 25-methyl-2-butyl group, a 26-methyl-2-butyl group, a 27-methyl-2-butyl group, a 28-methyl-2-butyl group, a 29-methyl-2-butyl group, a 30-methyl-2-butyl group, a 31-methyl-2-butyl group, a 32-methyl-2-butyl group, a 33-methyl-2-butyl group, a 34-methyl-2-butyl group, a 35-methyl-2-butyl group, a 36-methyl-2-butyl group, a 37-methyl-2-butyl group, a 38-methyl-2-butyl Examples of the linear unsaturated aliphatic hydrocarbon group having 1 to 20 carbon atoms include vinyl and 2-propenyl groups. These groups can be used alone or in combination.

[0065] Examples of cyclic aliphatic hydrocarbon groups having 3 to 20 carbon atoms include saturated cyclic aliphatic hydrocarbon groups having 3 to 20 carbon atoms and unsaturated cyclic aliphatic hydrocarbon groups having 3 to 20 carbon atoms. Examples of saturated cyclic aliphatic hydrocarbon groups having 3 to 20 carbon atoms include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, and cyclodecyl groups. Examples of unsaturated cyclic aliphatic hydrocarbon groups having 3 to 20 carbon atoms include cyclopentenyl and cyclohexenyl groups. These can be used alone or in combination of two or more.

[0066] Examples of aromatic hydrocarbon groups include aromatic hydrocarbon groups having 6 to 20 carbon atoms. Examples of aromatic hydrocarbon groups having 6 to 20 carbon atoms include phenyl, 2-tolyl, 3-tolyl, 4-tolyl, 2,3-xylyl, 2,4-xylyl, 2,5-xylyl, 2,6-xylyl, 3,4-xylyl, 3,5-xylyl, 2,3,4-trimethylphenyl, 3,4,5-trimethylphenyl, 2,4,6-trimethylphenyl, 2,3,4,5-tetramethylphenyl, 2,3,4,6-tetramethylphenyl, 2-ethylphenyl, 3-ethylphenyl, 4-ethylphenyl, 1-naphthyl, and 2-naphthyl. These groups can be used alone or in combination of two or more.

[0067] Examples of aromatic aliphatic hydrocarbon groups include aromatic aliphatic hydrocarbon groups having 7 to 20 carbon atoms. Examples of aromatic aliphatic hydrocarbon groups having 7 to 20 carbon atoms include benzyl, 1-phenylethyl, 2-phenylethyl, 1-phenylpropyl, 2-phenylpropyl, 3-phenylpropyl, o-methylbenzyl, m-methylbenzyl, p-methylbenzyl, o-ethylbenzyl, m-ethylbenzyl, p-ethylbenzyl, o-isopropylbenzyl, m-isopropylbenzyl, p-isopropylbenzyl, 2,3,4-trimethylbenzyl, 3,4,5-trimethylbenzyl, and 2,4,6-trimethylbenzyl. These can be used alone or in combination of two or more.

[0068] The aliphatic hydrocarbon group, aromatic hydrocarbon group, and araliphatic hydrocarbon group may have a substituent. Examples of the substituent include a halogeno group, a cyano group, an amino group, a carboxy group, a sulfonyl group, and an alkoxy group. These may be used alone or in combination of two or more. The number of substituents is appropriately determined depending on the purpose and application. The substitution position is appropriately determined depending on the purpose and application.

[0069] The compound of formula (1) has three or more SXR groups depending on the value of n. The Rs contained in each SXR group may be the same as or different from each other. Preferably, one selected from the group consisting of an aliphatic hydrocarbon group, an aromatic hydrocarbon group, and an araliphatic hydrocarbon group is used alone. That is, preferably, in formula (1), the Rs contained in each SXR group are the same as each other.

[0070] When R represents an aliphatic hydrocarbon group, it is preferably a linear aliphatic hydrocarbon group having 1 to 10 carbon atoms, more preferably a linear aliphatic hydrocarbon group having 1 to 4 carbon atoms, even more preferably a linear aliphatic hydrocarbon group having 1 to 2 carbon atoms, and particularly preferably a methyl group.

[0071] When R represents an aromatic hydrocarbon group, it is preferably an aromatic hydrocarbon group having 6 to 10 carbon atoms, more preferably an aromatic hydrocarbon group having 6 to 8 carbon atoms, and even more preferably a phenyl group.

[0072] When R represents an aromatic aliphatic hydrocarbon group, it is preferably an aromatic aliphatic hydrocarbon group having 7 to 15 carbon atoms, more preferably an aromatic aliphatic hydrocarbon group having 7 to 10 carbon atoms, and even more preferably a benzyl group or a 2-phenylethyl group.

[0073] From the viewpoint of obtaining a cured product having a well-balanced refractive index and flexibility, in the above formula (1), R preferably represents a methyl group, a phenyl group, or a benzyl group. That is, when R is a methyl group, a phenyl group, or a benzyl group, a cured product having both an especially excellent refractive index and especially excellent flexibility can be obtained.

[0074] From the viewpoint of refractive index, R more preferably represents a phenyl group or a benzyl group, and from the viewpoint of flexibility, R more preferably represents a methyl group.

[0075] Furthermore, from the viewpoint of obtaining excellent weather resistance in addition to an excellent refractive index and excellent flexibility, in the above formula (1), preferably, X represents a carbonyl group and R represents an aromatic-aliphatic hydrocarbon group and / or an aliphatic hydrocarbon group, more preferably, X represents a carbonyl group and R represents an aromatic-aliphatic hydrocarbon group. That is, when X is a carbonyl group and R is an aromatic-aliphatic hydrocarbon group, a cured product having an especially excellent refractive index, especially excellent flexibility, and especially excellent weather resistance can be obtained.

[0076] From the viewpoint of refractive index, it is more preferable that X represents a carbonyl group and R represents a benzyl group. Furthermore, from the viewpoint of flexibility and weather resistance, it is more preferable that X represents a carbonyl group and R represents a 2-phenylethyl group and / or a methyl group, and it is particularly preferable that X represents a carbonyl group and R represents a 2-phenylethyl group.

[0077] (6) Specific examples A preferred example of the compound represented by the above formula (1) is a compound in which A in formula (1) is a GST residue. The compound in formula (1) in which A is a GST residue is represented, for example, by the following general formula (2): General formula (2);

[0078] [ka] (In formula (2), S, X, and R have the same meanings as S, X, and R in formula (1). In formula (2), the portion surrounded by a dashed line represents the organic group A (n=3) in formula (1).)

[0079] The compound represented by the above formula (2) gives a cured product that has both an especially excellent refractive index and especially excellent flexibility.

[0080] A more specific example of the compound represented by formula (2) is 4-benzylthiomethyl-1,8-bisbenzylthio-3,6-dithiaoctane (Bn-GST), in which X in formula (2) represents a single bond and R represents a benzyl group.

[0081] A more specific example of the compound represented by formula (2) is 4-benzoylthiomethyl-1,8-bisbenzoylthio-3,6-dithiaoctane (Bz-GST), in which X in formula (2) represents a carbonyl group and R represents a phenyl group.

[0082] A more specific example of the compound represented by formula (2) is 4-acetylthiomethyl-1,8-bisacetylthio-3,6-dithiaoctane (Ac-GST), in which X in formula (2) represents a carbonyl group and R represents a methyl group.

[0083] A more specific example of the compound represented by formula (2) is 4-phenylacetylthiomethyl-1,8-bisphenylacetylthio-3,6-dithiaoctane (PA-GST), in which X in formula (2) represents a carbonyl group and R represents a benzyl group.

[0084] A more specific example of the compound represented by formula (2) is 4-(3-phenylpropionyl)thiomethyl-1,8-bis(3-phenylpropionyl)thio-3,6-dithiaoctane (PP-GST). In PP-GST, X in formula (2) represents a carbonyl group, and R represents a 2-phenylethyl group.

[0085] Furthermore, preferred examples of the compound represented by the above formula (1) include compounds in which A in formula (1) is an FSH residue. The compound in formula (1) in which A is an FSH residue is represented, for example, by the following general formula (3). General formula (3);

[0086] [ka] (In formula (3), S, X, and R have the same meanings as S, X, and R in formula (1). In formula (3), the portion surrounded by a dashed line represents the organic group A (n=4) in formula (1).)

[0087] The compound represented by the above formula (3) gives a cured product that has both an especially excellent refractive index and especially excellent flexibility.

[0088] A more specific example of the compound represented by formula (3) is 5,7-bis(benzoylmercaptomethyl)-1,11-bis(benzoylmercapto)-3,6,9-trithiaundecane (Bz-FSH). In Bz-FSH, X in formula (3) represents a single bond, and R represents a benzyl group.

[0089] 2. Compound manufacturing method (1) Raw materials for compounds The above compound is produced, for example, by reacting the above tri- or higher functional sulfur-containing polythiol with a modifier.

[0090] The modifying agent is a compound that modifies the mercapto groups of the above-mentioned tri- or higher functional sulfur-containing polythiol to the SXR groups in the above formula (1).

[0091] The modifying agent may be, for example, a compound represented by the following general formula (6). General formula (6);

[0092] [ka] (In formula (6), X and R have the same meanings as X and R in formula (1). Y represents a halogen or a hydroxyl group.)

[0093] In the above formula (6), X and R have the same meanings as X and R in formula (1). Y represents a halogen or a hydroxyl group. Examples of halogen include fluorine, chlorine, bromine, and iodine. Preferred examples of halogen include chlorine and bromine.

[0094] In the above formula (6), when Y is a halogen and X is a single bond, examples of the modifying agent include halogenated hydrocarbons. Examples of the modifying agent include alkyl halides, aryl halides, and aralkyl halides. Examples of the alkyl halides include methyl fluoride, methyl chloride, methyl bromide, methyl iodide, ethyl fluoride, ethyl chloride, ethyl bromide, and ethyl iodide. Examples of the aryl halides include phenyl fluoride, phenyl chloride, phenyl bromide, and phenyl iodide. Examples of the aralkyl halides include benzyl fluoride, benzyl chloride, benzyl bromide (benzyl bromide), and benzyl iodide. These may be used alone or in combination of two or more. Preferably, the modifying agent is an aralkyl halide, more preferably benzyl bromide (benzyl bromide).

[0095] In the above formula (6), when Y is a halogen and X is a carbonyl group, the modifying agent may be an acyl halide. Examples of the acyl halide include acetyl fluoride, acetyl chloride, acetyl bromide, acetyl iodide, benzoyl fluoride, benzoyl chloride, benzoyl bromide, and benzoyl iodide. These may be used alone or in combination of two or more. A preferred example of the modifying agent is benzoyl chloride.

[0096] In the above formula (6), when Y is a hydroxyl group and X is a carbonyl group, the modifier may be a carboxylic acid. Examples of the carboxylic acid include monocarboxylic acids and their anhydrides. Examples of the monocarboxylic acid include aliphatic monocarboxylic acids, aromatic monocarboxylic acids, and araliphatic monocarboxylic acids. Examples of the aliphatic monocarboxylic acids include acetic acid, propionic acid, butyric acid, caproic acid, octylic acid, lauric acid, myristic acid, palmitic acid, stearic acid, 2-ethylhexanoic acid, cyclohexanecarboxylic acid, and cyclopentanecarboxylic acid. Examples of the aromatic monocarboxylic acids include benzoic acid and toluic acid. Examples of the araliphatic monocarboxylic acids include diphenylacetic acid. These may be used alone or in combination of two or more. Preferably, the modifier includes aliphatic monocarboxylic acids and their anhydrides, more preferably acetic acid and its anhydrides, and even more preferably acetic anhydride.

[0097] (2) Mixing ratio and reaction conditions The trifunctional or higher sulfur-containing polythiol and the modifier are mixed in an appropriate ratio and reacted under appropriate conditions. The mixing ratio of the trifunctional or higher sulfur-containing polythiol and the modifier is selected depending on the type of the trifunctional or higher sulfur-containing polythiol and the type of the modifier. Examples of the reaction between the trifunctional or higher sulfur-containing polythiol and the modifier include nucleophilic substitution reaction, nucleophilic acylation reaction, cross-coupling reaction, and dehydration condensation reaction.

[0098] For example, when the modifier contains a halogenated hydrocarbon, the trifunctional or higher sulfur-containing polythiol and the modifier undergo a nucleophilic substitution reaction in the presence of a known basic compound to produce the compound of formula (1). More specifically, the basic compound eliminates protons from the trifunctional or higher sulfur-containing polythiol to produce a nucleophile. The nucleophile derived from the trifunctional or higher sulfur-containing polythiol then undergoes a nucleophilic substitution reaction with the halogenated hydrocarbon. Examples of basic compounds include metal alcoholates and amine compounds. In such a reaction, the blending ratio of the trifunctional or higher sulfur-containing polythiol and the modifier is adjusted based on the equivalent ratio of halogen atoms in the modifier (halogenated hydrocarbon) to mercapto groups in the sulfur-containing polythiol. The equivalent ratio of halogen atoms in the modifier (halogenated hydrocarbon) to mercapto groups in the sulfur-containing polythiol (halogen atoms / mercapto groups) is, for example, 0.9 or more, preferably 1.0 or more, and more preferably 1.01 or more. The equivalent ratio (halogen atoms / mercapto groups) of halogen atoms in the modifying agent (halogenated hydrocarbon) to mercapto groups in the sulfur-containing polythiol is, for example, 5.0 or less, preferably 3.0 or less, and more preferably 1.5 or less.

[0099] When the modifying agent contains a halogenated hydrocarbon, the reaction conditions for the nucleophilic substitution reaction are appropriately selected depending on the type of trifunctional or higher sulfur-containing polythiol and the type of modifying agent. For example, the reaction temperature is, for example, -20°C or higher, preferably -10°C or higher. The reaction temperature is, for example, 50°C or lower, preferably 30°C or lower. The reaction time is, for example, 3 hours or longer, preferably 6 hours or longer. The reaction time is, for example, 48 hours or shorter, preferably 24 hours or shorter. The trifunctional or higher sulfur-containing polythiol and the modifying agent may react without a solvent or in the presence of a known solvent. The type and amount of the solvent are appropriately determined. The trifunctional or higher sulfur-containing polythiol and the modifying agent may react without a catalyst or in the presence of a known catalyst. The type and amount of the catalyst are appropriately determined.

[0100] Furthermore, for example, when the modifying agent contains an acyl halide, the trifunctional or higher sulfur-containing polythiol and the modifying agent undergo a nucleophilic acylation reaction in the presence of the basic compound described above to produce the compound of formula (1). More specifically, the basic compound eliminates protons from the trifunctional or higher sulfur-containing polythiol to produce a nucleophile. The nucleophile derived from the trifunctional or higher sulfur-containing polythiol then undergoes a nucleophilic acylation reaction with the acyl halide. In such a reaction, the blending ratio of the trifunctional or higher sulfur-containing polythiol and the modifying agent is adjusted based on the equivalent ratio of halogen atoms in the modifying agent (acyl halide) to mercapto groups in the sulfur-containing polythiol. The equivalent ratio of halogen atoms in the modifying agent (acyl halide) to mercapto groups in the sulfur-containing polythiol (halogen atoms / mercapto groups) is, for example, 0.9 or more, preferably 1.0 or more, and more preferably 1.05 or more. The equivalent ratio (halogen atom / mercapto group) of the halogen atom in the modifying agent (acyl halide) to the mercapto group in the sulfur-containing polythiol is, for example, 5.0 or less, preferably 3.0 or less, and more preferably 1.5 or less.

[0101] When the modifying agent contains an acyl halide, the reaction conditions for the nucleophilic acylation reaction are appropriately selected depending on the type of trifunctional or higher sulfur-containing polythiol and the type of modifying agent. For example, the reaction temperature is, for example, -20°C or higher, preferably -10°C or higher. The reaction temperature is, for example, 50°C or lower, preferably 30°C or lower. The reaction time is, for example, 3 hours or longer, preferably 6 hours or longer. The reaction time is, for example, 48 hours or shorter, preferably 24 hours or shorter. The trifunctional or higher sulfur-containing polythiol and the modifying agent may react without a solvent or in the presence of a known solvent. The type and amount of the solvent are appropriately determined. The trifunctional or higher sulfur-containing polythiol and the modifying agent may react without a catalyst or in the presence of a known catalyst. The type and amount of the catalyst are appropriately determined.

[0102] Furthermore, for example, when the modifier contains a carboxylic acid, the trifunctional or higher sulfur-containing polythiol and the modifier (carboxylic acid) undergo a dehydration condensation reaction in the presence of the basic compound to produce the compound of formula (1). In such a reaction, the blending ratio of the trifunctional or higher sulfur-containing polythiol and the modifier is adjusted based on the equivalent ratio of the carboxy groups in the modifier (carboxylic acid) to the mercapto groups in the sulfur-containing polythiol. The equivalent ratio of the carboxy groups in the modifier (carboxylic acid) to the mercapto groups in the sulfur-containing polythiol (carboxy groups / mercapto groups) is, for example, 0.9 or more, preferably 1.0 or more, and more preferably 1.05 or more. The equivalent ratio of the carboxy groups in the modifier (carboxylic acid) to the mercapto groups in the sulfur-containing polythiol (carboxy groups / mercapto groups) is, for example, 5.0 or less, preferably 3.0 or less, and more preferably 2.5 or less.

[0103] When the modifying agent contains a carboxylic acid, the reaction conditions for the dehydration condensation reaction are appropriately selected depending on the type of trifunctional or higher sulfur-containing polythiol and the type of modifying agent. For example, the reaction temperature is, for example, -20°C or higher, preferably -10°C or higher. The reaction temperature is, for example, 50°C or lower, preferably 30°C or lower. The reaction time is, for example, 3 hours or longer, preferably 6 hours or longer. The reaction time is, for example, 48 hours or shorter, preferably 24 hours or shorter. The trifunctional or higher sulfur-containing polythiol and the modifying agent may react without a solvent or in the presence of a known solvent. The type and amount of the solvent are appropriately determined. The trifunctional or higher sulfur-containing polythiol and the modifying agent may react without a catalyst or in the presence of a known catalyst. The type and amount of the catalyst are appropriately determined.

[0104] After the reaction is complete, if necessary, a known neutralizing agent is added to the reaction product solution to adjust the pH of the reaction product solution. If necessary, the reaction product is concentrated or isolated by a known method. If necessary, the reaction product is purified by a known method. This yields the compound represented by formula (1) as the reaction product.

[0105] The modifier and reaction method are not limited to those described above. For example, the reaction method may be an ene-thiol reaction. For example, the modifier may be a compound capable of undergoing an ene-thiol reaction with the above-mentioned trifunctional or higher sulfur-containing polythiol. Examples of such compounds include vinyl compounds. Examples of vinyl compounds include styrene, methylstyrene, and butylstyrene. These compounds may be used alone or in combination.

[0106] When a vinyl compound is used as the modifier, a tri- or higher functional sulfur-containing polythiol and the modifier (vinyl compound) undergo an ene-thiol reaction in the presence of a known radical initiator to produce a compound of the above formula (1) (X represents a single bond, and R represents a hydrocarbon group derived from the vinyl compound).

[0107] In the ene-thiol reaction, a radical polymerization initiator abstracts a hydrogen atom from the mercapto group of a trifunctional or higher sulfur-containing polythiol, generating a thiyl radical. The thiyl radical undergoes radical addition to the vinyl group of a vinyl compound, generating a carboradical. The carboradical then abstracts a hydrogen atom from another mercapto group, completing the alkylation of the mercapto group. This also continues the radical chain reaction. As a result, the compound of formula (1) is obtained.

[0108] The radical polymerization initiator is not particularly limited, and examples thereof include known radical polymerization initiators. More specific examples of radical polymerization initiators include photoradical polymerization initiators and thermal radical polymerization initiators. Examples of photoradical polymerization initiators include 1-hydroxycyclohexane-1-yl phenyl ketone. Examples of thermal radical polymerization initiators include organic peroxides and azo compounds. Examples of organic peroxides include benzoyl peroxide. Examples of azo compounds include azobisisobutyronitrile. These can be used alone or in combination of two or more types. The blending ratio of the radical polymerization initiator is appropriately set depending on the type of radical polymerization initiator.

[0109] In the ene-thiol reaction, the blending ratio of the trifunctional or higher sulfur-containing polythiol and the modifier is adjusted based on the equivalent ratio of the vinyl group in the modifier (vinyl compound) to the mercapto group in the sulfur-containing polythiol. The equivalent ratio of the vinyl group in the modifier (vinyl compound) to the mercapto group in the sulfur-containing polythiol (vinyl group / mercapto group) is, for example, 0.9 or more, preferably 1.0 or more, more preferably 1.01 or more. In addition, the equivalent ratio of the vinyl group in the modifier (vinyl compound) to the mercapto group in the sulfur-containing polythiol (vinyl group / mercapto group) is, for example, 5.0 or less, preferably 3.0 or less, more preferably 1.5 or less.

[0110] The reaction conditions for the ene-thiol reaction are appropriately selected depending on the type of trifunctional or higher sulfur-containing polythiol and the type of modifier. For example, the reaction temperature is, for example, -20°C or higher, preferably -10°C or higher. The reaction temperature is, for example, 150°C or lower, preferably 100°C or lower. The reaction time is, for example, 3 hours or longer, preferably 6 hours or longer. The reaction time is, for example, 48 hours or shorter, preferably 24 hours or shorter. The trifunctional or higher sulfur-containing polythiol and the modifier may react without a solvent or in the presence of a known solvent. The type and amount of the solvent are appropriately determined. The trifunctional or higher sulfur-containing polythiol and the modifier may react without a catalyst or in the presence of a known catalyst. The type and amount of the catalyst are appropriately determined.

[0111] After the reaction is completed, the reaction product is concentrated or isolated by a known method, if necessary. Furthermore, the reaction product is purified by a known method, if necessary. As a result, the compound represented by formula (1) is obtained as the reaction product.

[0112] The above compound is a novel compound and has a specific structure represented by the above formula (1). Examples of uses of such compounds include additives. That is, additives preferably contain the above compound. More specific examples of additives include plasticizers and refractive index adjusters, and plasticizers are preferred. That is, plasticizers preferably contain the above compound. In other words, the above compound is preferably used as a plasticizer. The above compound can be used to obtain a cured product (described below) that has both a refractive index and flexibility.

[0113] 3.Curable composition (1) Main component The curable composition contains a plasticizer and a curable compound as main components. The main component is a component whose content relative to the total is a predetermined value or more. The content ratio of the main component relative to the total is, for example, 90% by mass or more. In other words, the total solid content of the plasticizer and the curable compound is 90% by mass or more relative to the total solid content of the curable composition.

[0114] The curable compound is an uncured compound that is cured by a known method to produce a cured resin (described later). The plasticizer is an additive that improves the flexibility of the cured resin (described later). The plasticizer and the curable compound are described in detail below.

[0115] (2) Plasticizer The plasticizer contains a compound represented by the above formula (1), and preferably consists of a compound represented by the above formula (1).

[0116] If the plasticizer contains a compound represented by the above formula (1), the plasticizer can improve the flexibility of the cured product (described later) and can suppress a decrease in the refractive index of the cured product (described later) or can improve the refractive index.

[0117] (3) Curable compound The curable compound is not particularly limited, and examples thereof include resin raw materials capable of producing a cured resin (described below).

[0118] As described below, examples of the cured resin include cured polyurethane resin, cured polyolefin resin, cured polyamine resin, cured amide resin, cured urea resin, cured phenolic resin, cured epoxy resin, cured acrylic resin, cured melamine resin, and cured alkyd resin. These may be used alone or in combination of two or more.

[0119] As the curable resin (described later), preferably, a curable polyurethane resin or a curable acrylic resin is used, and the curable compound is selected depending on the type of the curable resin (described later).

[0120] For example, when a cured polyurethane resin is used as the curable resin, the curable compound may be, for example, a polyurethane resin raw material, or when a cured acrylic resin is used as the curable resin, the curable compound may be, for example, an acrylic resin raw material.

[0121] The polyurethane resin raw material and the acrylic resin raw material will be described in detail below.

[0122] (3-1) Polyurethane resin raw materials The polyurethane resin raw material is an uncured (unreacted) resin composition for producing a cured polyurethane resin (described later). The polyurethane resin raw material includes, for example, polyisocyanate and polyol.

[0123] (3-2) Polyisocyanate Polyisocyanates have multiple isocyanate groups in one molecule, and examples of polyisocyanates include polyisocyanate monomers and polyisocyanate derivatives.

[0124] Examples of polyisocyanate monomers include aliphatic polyisocyanates, aromatic polyisocyanates, and araliphatic polyisocyanates.

[0125] Examples of aliphatic polyisocyanates include ethylene diisocyanate, trimethylene diisocyanate, 1,4-tetramethylene diisocyanate, 1,5-pentamethylene diisocyanate, 1,6-hexamethylene diisocyanate, trimethylhexamethylene diisocyanate, and 2,6-diisocyanate methyl caproate. These can be used alone or in combination of two or more.

[0126] Aliphatic polyisocyanate monomers also include alicyclic polyisocyanate monomers. Examples of alicyclic polyisocyanate monomers include 1,3-cyclopentane diisocyanate, 1,3-cyclopentene diisocyanate, 1,4-cyclohexane diisocyanate, 1,3-cyclohexane diisocyanate, 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate, methylenebis(cyclohexyl isocyanate), methyl-2,4-cyclohexane diisocyanate, methyl-2,6-cyclohexane diisocyanate, norbornane diisocyanate, and bis(isocyanatomethyl)cyclohexane. These can be used alone or in combination of two or more.

[0127] Examples of aromatic polyisocyanates include tolylene diisocyanate, phenylene diisocyanate, 4,4'-diphenyl diisocyanate, 1,5-naphthalene diisocyanate, and diphenylmethane diisocyanate. a These may be used alone or in combination of two or more.

[0128] Examples of aromatic aliphatic polyisocyanates include xylylene diisocyanate, tetramethylxylylene diisocyanate, and ω,ω'-diisocyanato-1,4-diethylbenzene. These can be used alone or in combination of two or more.

[0129] The polyisocyanate derivative is derived from the polyisocyanate monomer described above. Examples of the polyisocyanate derivative include isocyanurate-modified products, iminooxadiazinedione-modified products, triol adducts, allophanate-modified products, biuret-modified products, urea-modified products, oxadiazinetrione-modified products, carbodiimide-modified products, uretdione-modified products, and uretonimine-modified products. These can be used alone or in combination of two or more types. A preferred example of the polyisocyanate derivative is an isocyanurate-modified product.

[0130] The polyisocyanate may be used alone or in combination of two or more kinds. The polyisocyanate preferably contains a polyisocyanate derivative, and more preferably consists of a polyisocyanate derivative.

[0131] As the polyisocyanate derivative, from the viewpoint of improving the refractive index and transparency, a polyisocyanate derivative derived from an araliphatic polyisocyanate (araliphatic polyisocyanate derivative) is preferably used.

[0132] As the aromatic aliphatic polyisocyanate derivative, a derivative of xylylene diisocyanate is more preferred, and a triol adduct of xylylene diisocyanate is even more preferred.

[0133] The average number of isocyanate groups in the polyisocyanate is, for example, 2 or more, or preferably 2.5 or more. The average number of isocyanate groups in the polyisocyanate is, for example, 4 or less, or preferably 3.5 or less.

[0134] The polyisocyanate has an isocyanate group content (NCO%) of, for example, 5% by mass or more, or preferably 7% by mass or more, and an isocyanate group content (NCO%) of, for example, 30% by mass or less, or preferably 25% by mass or less.

[0135] (3-3) Polyol The polyol includes, for example, a macropolyol. A macropolyol has two or more hydroxyl groups in one molecule. A macropolyol is a relatively high molecular weight organic compound. The number average molecular weight of a macropolyol is, for example, 400 or more and, for example, 20,000 or less. The number average molecular weight can be calculated by a known method from the hydroxyl group equivalent weight and the average number of hydroxyl groups. The number average molecular weight can also be measured as a polystyrene-equivalent molecular weight by gel permeation chromatography (the same applies hereinafter).

[0136] Examples of macropolyols include polyether polyols, polyester polyols, polycarbonate polyols, polyurethane polyols, epoxy polyols, vegetable oil polyols, polyolefin polyols, acrylic polyols, and vinyl monomer-modified polyols. These macropolyols can be used alone or in combination of two or more.

[0137] The number average molecular weight of the macropolyol is, for example, more than 400, preferably 500 or more, more preferably 1000 or more. The number average molecular weight of the macropolyol is, for example, 20000 or less, preferably 15000 or less, more preferably 10000 or less, and even more preferably 5000 or less.

[0138] The hydroxyl value of the macropolyol is, for example, 5 mgKOH / g or more, preferably 10 mgKOH / g or more, more preferably 15 mgKOH / g or more, and even more preferably 20 mgKOH / g or more. The hydroxyl value of the macropolyol is, for example, 500 mgKOH / g or less, preferably 300 mgKOH / g or less, more preferably 200 mgKOH / g or less, even more preferably 100 mgKOH / g or less, and particularly preferably 50 mgKOH / g or less. The hydroxyl value is measured in accordance with the description of JIS K 1557-1 (2007) (the same applies hereinafter).

[0139] As the macropolyol, preferably, an acrylic polyol is used.

[0140] The acrylic polyol may be, for example, a copolymer of an acrylic raw material component, which contains, for example, a hydroxyl group-containing (meth)acrylate and a copolymerizable vinyl monomer.

[0141] The term "(meth)acrylate" refers to an acrylate and / or a methacrylate, and the term "copolymerizable vinyl monomer" refers to a vinyl monomer that can be polymerized with a hydroxyl group-containing (meth)acrylate.

[0142] The hydroxyl group-containing (meth)acrylate contains a hydroxyl group and an alkyl group. Examples of the alkyl group include alkyl groups having 1 to 4 carbon atoms. Specific examples of the hydroxyalkyl (meth)acrylate include 2-hydroxyethyl (meth)acrylate, hydroxypropyl (meth)acrylate, hydroxybutyl (meth)acrylate, and 2,2-dihydroxymethylbutyl (meth)acrylate. These may be used alone or in combination of two or more. Preferred examples of the hydroxyl group-containing (meth)acrylate include hydroxyalkyl (meth)acrylate, more preferably 2-hydroxyethyl (meth)acrylate, and even more preferably 2-hydroxyethyl methacrylate.

[0143] Examples of copolymerizable vinyl monomers include alkyl(meth)acrylates. Alkyl(meth)acrylates do not contain a hydroxyl group but contain an alkyl group. Examples of the alkyl group include alkyl groups having 1 to 4 carbon atoms and alkyl groups having 5 to 8 carbon atoms. Examples of alkyl(meth)acrylates having an alkyl group having 1 to 4 carbon atoms include methyl(meth)acrylate, ethyl(meth)acrylate, propyl(meth)acrylate, isopropyl(meth)acrylate, butyl(meth)acrylate, isobutyl(meth)acrylate, s-butyl(meth)acrylate, and t-butyl(meth)acrylate. Examples of alkyl(meth)acrylates having an alkyl group having 5 to 8 carbon atoms include pentyl(meth)acrylate, isopentyl(meth)acrylate, hexyl(meth)acrylate, 2-ethylhexyl(meth)acrylate, and cyclohexyl(meth)acrylate. These can be used alone or in combination of two or more.

[0144] Examples of copolymerizable vinyl monomers include aromatic ring-containing vinyl monomers. Examples of aromatic ring-containing vinyl monomers include aromatic ring-containing (meth)acrylates. Aromatic ring-containing (meth)acrylates contain an aromatic ring. Examples of aromatic rings include a benzene ring, a naphthalene ring, an anthracene ring, and a phenanthrene ring. More specific examples of aromatic ring-containing (meth)acrylates include benzyl (meth)acrylate, phenoxyethyl (meth)acrylate, m-phenoxybenzyl (meth)acrylate, and 1-naphthylmethyl (meth)acrylate. These can be used alone or in combination of two or more. Preferred examples of aromatic ring-containing (meth)acrylates include m-phenoxybenzyl (meth)acrylate and naphthylmethyl (meth)acrylate, and more preferred examples include m-phenoxybenzyl acrylate and naphthylmethyl acrylate. In addition to the above, examples of aromatic ring-containing vinyl monomers include styrene, α-methylstyrene, vinyltoluene, vinylbiphenyl, and divinylbenzene. These can be used alone or in combination of two or more. Preferred examples of aromatic ring-containing vinyl monomers include aromatic ring-containing (meth)acrylates.

[0145] Furthermore, examples of copolymerizable vinyl monomers include vinyl monomers containing functional groups (excluding hydroxyl groups). Examples of vinyl monomers containing functional groups (excluding hydroxyl groups) include carboxyl group-containing vinyl monomers, glycidyl group-containing vinyl monomers, amino group-containing vinyl monomers, cyano group-containing vinyl monomers, acetoacetoxy group-containing vinyl monomers, sulfonic acid group-containing vinyl monomers, and phosphate group-containing vinyl monomers. Examples of carboxyl group-containing vinyl monomers include acrylic acid. Examples of glycidyl group-containing vinyl monomers include glycidyl (meth)acrylate. Examples of amino group-containing vinyl monomers include 2-aminoethyl (meth)acrylate. Examples of cyano group-containing vinyl monomers include (meth)acrylonitrile. Examples of acetoacetoxy group-containing vinyl monomers include acetoacetoxyethyl (meth)acrylate. Examples of sulfonic acid group-containing vinyl monomers include allylsulfonic acid and its salts. Examples of phosphate group-containing vinyl monomers include 2-methacrylonitrile. R Examples of the vinyl monomer containing a functional group (excluding a hydroxyl group) include carboxyl group-containing vinyl monomers, and more preferably acrylic acid.

[0146] In addition to the above, copolymerizable vinyl monomers also include, for example, vinyl esters, N-substituted unsaturated carboxylic acid amides, heterocyclic vinyl compounds, vinylidene halides, α-olefins, dienes, and crosslinkable vinyl monomers. Examples of crosslinkable vinyl monomers include polyfunctional (meth)acrylates, more specifically, bifunctional (meth)acrylates, trifunctional (meth)acrylates, and tetrafunctional or higher functional (meth)acrylates. Examples of bifunctional (meth)acrylates include ethylene glycol di(meth)acrylate, butylene glycol di(meth)acrylate, hexanediol di(meth)acrylate, and oligoethylene glycol di(meth)acrylate. Examples of trifunctional (meth)acrylates include trimethylolpropane tri(meth)acrylate. Examples of tetrafunctional or higher functional (meth)acrylates include pentaerythritol tetra(meth)acrylate. These may be used alone or in combination.

[0147] These copolymerizable vinyl monomers may be used alone or in combination of two or more.

[0148] The copolymerizable vinyl monomer is preferably an aromatic ring-containing vinyl monomer. If the copolymerizable vinyl monomer contains an aromatic ring-containing vinyl monomer, the acrylic polyol contains an aromatic ring. In other words, the acrylic polyol is preferably an aromatic ring-containing acrylic polyol. The aromatic ring-containing acrylic polyol can provide a cured product (described later) having an excellent refractive index and excellent flexibility.

[0149] Furthermore, as the copolymerizable vinyl monomer, a carboxy group-containing vinyl monomer is preferably used. If the acrylic polyol contains a carboxy group-containing vinyl monomer, the acrylic polyol contains a carboxy group. In other words, the acrylic polyol is preferably a carboxy group-containing acrylic polyol. The carboxy group-containing acrylic polyol can provide a cured product (described later) having an excellent refractive index and excellent flexibility.

[0150] The blending ratio of the hydroxyl group-containing (meth)acrylate and the copolymerizable vinyl monomer is appropriately set depending on the purpose and application. For example, the hydroxyl group-containing (meth)acrylate is, for example, 1 part by mass or more, preferably 3 parts by mass or more, per 100 parts by mass of the total of the hydroxyl group-containing (meth)acrylate and the copolymerizable vinyl monomer. Furthermore, the hydroxyl group-containing (meth)acrylate is, for example, 30 parts by mass or less, preferably 10 parts by mass or less, per 100 parts by mass of the total of the hydroxyl group-containing (meth)acrylate and the copolymerizable vinyl monomer.

[0151] The total amount of the copolymerizable vinyl monomer is, for example, 70 parts by mass or more, preferably 90 parts by mass or more, relative to 100 parts by mass of the total amount of the hydroxyl group-containing (meth)acrylate and the copolymerizable vinyl monomer. The total amount of the copolymerizable vinyl monomer is, for example, 99 parts by mass or less, preferably 97 parts by mass or less, relative to 100 parts by mass of the total amount of the hydroxyl group-containing (meth)acrylate and the copolymerizable vinyl monomer.

[0152] More specifically, when an aromatic ring-containing vinyl monomer is used, the amount of the aromatic ring-containing vinyl monomer is, for example, 70 parts by mass or more, preferably 90 parts by mass or more, relative to 100 parts by mass of the total amount of the hydroxyl group-containing (meth)acrylate and the copolymerizable vinyl monomer. Also, the amount of the aromatic ring-containing vinyl monomer is, for example, 99 parts by mass or less, preferably 97 parts by mass or less, relative to 100 parts by mass of the total amount of the hydroxyl group-containing (meth)acrylate and the copolymerizable vinyl monomer.

[0153] Furthermore, when a carboxyl group-containing vinyl monomer is used, the content ratio of the carboxyl group-containing vinyl monomer is appropriately set so that the total of the acid value and hydroxyl value of the acrylic polyol (carboxyl group-containing acrylic polyol) falls within the range described below.

[0154] For example, the amount of the carboxyl group-containing vinyl monomer is, for example, 1 part by mass or more, preferably 5 parts by mass or more, relative to 100 parts by mass of the total amount of the hydroxyl group-containing (meth)acrylate and the copolymerizable vinyl monomer. Also, the amount of the carboxyl group-containing vinyl monomer is, for example, 99 parts by mass or less, preferably 97 parts by mass or less, relative to 100 parts by mass of the total amount of the hydroxyl group-containing (meth)acrylate and the copolymerizable vinyl monomer.

[0155] The method for producing the acrylic polyol is not particularly limited. For example, the above-mentioned acrylic raw material components are copolymerized in the presence of a known organic solvent. Examples of the organic solvent include toluene. The blending ratio and blending timing of the organic solvent are appropriately set depending on the purpose and application.

[0156] In the production of acrylic polyol, a known polymerization initiator is used as necessary. Examples of the polymerization initiator include known radical polymerization initiators (described later), more preferably azo compounds (described later) and peroxides (described later), even more preferably peroxides (described later), and particularly preferably t-butylperoxy-2-ethylhexanoate. The blending ratio and blending timing of the polymerization initiator are appropriately set depending on the purpose and application.

[0157] The polymerization conditions for the acrylic raw material components are appropriately set depending on the purpose and application. For example, the polymerization temperature is, for example, 50°C or higher, preferably 70°C or higher. The polymerization temperature is, for example, 150°C or lower, preferably 130°C or lower. The polymerization time is, for example, 30 minutes or longer, preferably 1 hour or longer. The polymerization time is, for example, 12 hours or shorter, preferably 6 hours or shorter.

[0158] For example, when an organic solvent is used in the above polymerization method, a solution and / or dispersion of the acrylic polyol is obtained as the reaction product liquid.

[0159] The solids concentration of the acrylic polyol solution and / or dispersion can be adjusted by a known method. For example, an organic solvent can be added to the reaction product liquid as needed. Alternatively, a portion of the organic solvent can be removed from the reaction product liquid.

[0160] The solid content concentration of the acrylic polyol solution and / or dispersion is, for example, 30% by mass or more, preferably 40% by mass or more, and for example, 60% by mass or less, preferably 50% by mass or less.

[0161] The number average molecular weight of the acrylic polyol is, for example, more than 400, preferably 500 or more, and more preferably 1000 or more. The number average molecular weight of the acrylic polyol is, for example, 20000 or less, preferably 15000 or less, more preferably 10000 or less, and even more preferably 5000 or less.

[0162] The hydroxyl value of the acrylic polyol is, for example, 1 mgKOH / g or more, preferably 3 mgKOH / g or more. The hydroxyl value of the acrylic polyol is, for example, 500 mgKOH / g or less, preferably 300 mgKOH / g or less. The hydroxyl value is measured in accordance with the description of JIS K 1557-1 (2007) (the same applies hereinafter).

[0163] When the acrylic polyol does not contain a carboxyl group-containing acrylic polyol, the hydroxyl value of the acrylic polyol is preferably 5 mgKOH / g or more, more preferably 10 mgKOH / g or more, even more preferably 15 mgKOH / g or more, and particularly preferably 20 mgKOH / g or more. The hydroxyl value of the acrylic polyol is preferably 200 mgKOH / g or less, more preferably 100 mgKOH / g or less, and particularly preferably 50 mgKOH / g or less.

[0164] When the acrylic polyol contains a carboxyl group-containing acrylic polyol, the total acid value and hydroxyl value of the acrylic polyol (carboxyl group-containing acrylic polyol) is preferably 1 mgKOH / g or more, more preferably 3 mgKOH / g or more. The total acid value and hydroxyl value of the acrylic polyol (carboxyl group-containing acrylic polyol) is preferably 20 mgKOH / g or less, more preferably 10 mgKOH / g or less. The total acid value and hydroxyl value are measured in accordance with JIS K 1557-5 (2007) (hereinafter the same).

[0165] When the acrylic polyol contains a carboxyl group-containing acrylic polyol, the acid value of the acrylic polyol (carboxyl group-containing acrylic polyol) is, for example, 1 mgKOH / g or more, preferably 3 mgKOH / g or more. The acid value of the acrylic polyol (carboxyl group-containing acrylic polyol) is, for example, 20 mgKOH / g or less, preferably 10 mgKOH / g or less. The acid value is measured in accordance with the description of JIS K 1557-5 (2007) (the same applies hereinafter).

[0166] The polyol may include a low molecular weight polyol in addition to the macropolyol. The low molecular weight polyol has two or more hydroxyl groups in one molecule. The low molecular weight polyol is a relatively low molecular weight organic compound. The molecular weight of the low molecular weight polyol is, for example, 40 or more, for example, 400 or less.

[0167] Examples of low-molecular-weight polyols include dihydric alcohols, trihydric alcohols, and tetrahydric or higher alcohols. Examples of dihydric alcohols include ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, neopentyl glycol, diethylene glycol, triethylene glycol, and dipropylene glycol. Examples of trihydric alcohols include glycerin and trimethylolpropane. Examples of tetrahydric or higher alcohols include pentaerythritol and diglycerin. Examples of low-molecular-weight polyols include polymers obtained by addition polymerization of alkylene (C2-C3) oxides with dihydric to tetrahydric alcohols to give a number-average molecular weight of less than 400. These may be used alone or in combination of two or more. Examples of low-molecular-weight polyols include preferably dihydric alcohols and trihydric alcohols, and more preferably dihydric alcohols.

[0168] The polyols can be used alone or in combination of two or more. As the polyol, preferably, a macropolyol is used alone, and more preferably, an acrylic polyol is used alone.

[0169] (3-4) Form of polyurethane resin raw material Examples of the form of the polyurethane resin raw material include one-component curing polyurethane resin and two-component curing polyurethane resin. A preferred form of the polyurethane resin raw material is two-component curing polyurethane resin. A two-component curing polyurethane resin comprises an independent curing agent and a base component.

[0170] In the two-component curing polyurethane resin, the curing agent includes, for example, the above-mentioned polyisocyanate. In the two-component curing polyurethane resin, the base agent includes, for example, the above-mentioned polyol. The curing agent and base agent are mixed at the time of use to form a urethane cured product (cured resin described below). In the base agent, the polyol may be diluted with a known organic solvent. In the curing agent, the polyisocyanate may be diluted with a known organic solvent.

[0171] The two-component curing polyurethane resin preferably contains a base agent containing the above-mentioned acrylic polyol and a curing agent containing the above-mentioned polyisocyanate, thereby producing a cured product (described below) that has both an excellent refractive index and excellent flexibility.

[0172] The polyisocyanate and polyol undergo a urethane reaction by a known method to produce a cured polyurethane resin. In the urethane reaction, the blending ratio of the polyisocyanate and the polyol is adjusted, for example, based on the equivalent ratio (OH / NCO) of the hydroxyl groups in the polyol to the isocyanate groups in the polyisocyanate. The equivalent ratio (OH / NCO) of the hydroxyl groups in the polyol to the isocyanate groups in the polyisocyanate is, for example, 0.5 or more, preferably 0.8 or more, and more preferably 0.95 or more. Furthermore, the equivalent ratio (OH / NCO) of the hydroxyl groups in the polyol to the isocyanate groups in the polyisocyanate is, for example, 2.0 or less, preferably 1.5 or less, and more preferably 1.1 or less.

[0173] Furthermore, when the polyol contains the above-mentioned carboxyl group-containing acrylic polyol, the blending ratio of the polyisocyanate and the polyol is adjusted, for example, based on the equivalent ratio (OH+COOH / NCO) of the hydroxyl groups and carboxyl groups (total amount) in the polyol to the isocyanate groups in the polyisocyanate. The equivalent ratio (OH+COOH / NCO) of the hydroxyl groups and carboxyl groups (total amount) in the polyol to the isocyanate groups in the polyisocyanate is, for example, 0.5 or more, preferably 0.8 or more, and more preferably 0.95 or more. The equivalent ratio (OH+COOH / NCO) of the hydroxyl groups and carboxyl groups (total amount) in the polyol to the isocyanate groups in the polyisocyanate is, for example, 2.0 or less, preferably 1.5 or less, and more preferably 1.1 or less.

[0174] (3-5) Acrylic resin raw materials The acrylic resin raw material is a curable compound for producing a cured acrylic resin (described later) and contains, for example, a monomer component and a polymerization initiator.

[0175] (3-6) Monomer component The monomer component contains, for example, a radically polymerizable monomer, which is capable of generating a cured acrylic resin by radical polymerization.

[0176] The radical polymerizable monomer may be, for example, the monomers mentioned above as the raw material of acrylic polyol. More specifically, the radical polymerizable monomer may be, for example, the alkyl (meth)acrylate, the hydroxyl group-containing (meth)acrylate, the aromatic ring-containing vinyl monomer, the carboxyl group-containing vinyl monomer, the glycidyl group-containing vinyl monomer, the amino group-containing vinyl monomer, the cyano group-containing vinyl monomer, the acetoacetoxy group-containing vinyl monomer, the sulfonic acid group-containing vinyl monomer, and the phosphoric acid group-containing vinyl monomer. 、Examples of the vinyl esters include the vinyl esters, N-substituted unsaturated carboxylic acid amides, heterocyclic vinyl compounds, vinylidene halide compounds, α-olefins, dienes, and crosslinkable vinyl monomers. These may be used alone or in combination of two or more.

[0177] As the radical polymerizable monomer, preferably, a crosslinkable vinyl monomer is used, more preferably, a polyfunctional (meth)acrylate is used, even more preferably, a trifunctional (meth)acrylate is used, and particularly preferably, trimethylolpropane tri(meth)acrylate is used.

[0178] That is, the monomer component preferably contains a crosslinkable vinyl monomer, more preferably contains a polyfunctional (meth)acrylate, even more preferably contains a trifunctional (meth)acrylate, and particularly preferably contains trimethylolpropane tri(meth)acrylate.

[0179] Furthermore, the radical polymerizable monomer may preferably be a radical polymerizable monomer other than a crosslinkable vinyl monomer (hereinafter referred to as other monomer).

[0180] That is, the monomer component preferably contains a crosslinkable vinyl monomer and other monomers. The other monomers preferably include the alkyl(meth)acrylates and / or the aromatic ring-containing vinyl monomers.

[0181] The content ratio of the crosslinkable vinyl monomer and the other radical polymerizable monomer is appropriately set depending on the purpose and application.

[0182] For example, the content of the crosslinkable vinyl monomer relative to the total amount of the crosslinkable vinyl monomer and other radical polymerizable monomers is, for example, 10% by mass or more, preferably 20% by mass or more, more preferably 40% by mass or more, even more preferably 50% by mass or more, particularly preferably 60% by mass or more. Also, the content of the crosslinkable vinyl monomer relative to the total amount of the crosslinkable vinyl monomer and other radical polymerizable monomers is, for example, 99% by mass or less, preferably 90% by mass or less, more preferably 80% by mass or less, even more preferably 70% by mass or less, particularly preferably 65% ​​by mass or less.

[0183] For example, the content of the other radical polymerizable monomer relative to the total amount of the crosslinkable vinyl monomer and the other radical polymerizable monomer is, for example, 1% by mass or more, preferably 10% by mass or more, more preferably 20% by mass or more, even more preferably 30% by mass or more, and particularly preferably 35% by mass or more. Also, the content of the other radical polymerizable monomer relative to the total amount of the crosslinkable vinyl monomer and the other radical polymerizable monomer is, for example, 90% by mass or less, preferably 80% by mass or less, more preferably 60% by mass or less, even more preferably 50% by mass or less, and particularly preferably 40% by mass or less.

[0184] (3-7) Polymerization initiator The polymerization initiator may be a known radical polymerization initiator, such as an active energy ray radical polymerization initiator or a thermal radical polymerization initiator.

[0185] Examples of active energy ray radical polymerization initiators include photoradical polymerization initiators. Examples of photoradical polymerization initiators include alkylphenone-based photopolymerization initiators, acylphosphine oxide-based photopolymerization initiators, oxime ester-based photopolymerization initiators, carbazolephenone-based photopolymerization initiators, acridine-based photopolymerization initiators, triazine-based photopolymerization initiators, and benzoyl-based photopolymerization initiators. These can be used alone or in combination of two or more.

[0186] Examples of thermal radical polymerization initiators include azo compounds and peroxides. Examples of azo compounds include azoisobutyronitrile and dimethylazoisobutyrate. Examples of peroxides include benzoyl peroxide, ketone peroxide, peroxyketal, hydroperoxide, dialkyl peroxide, diacyl peroxide, peroxyester, t-butylperoxy-2-ethylhexanoate, and peroxydicarbonate. These can be used alone or in combination of two or more.

[0187] The active energy ray radical polymerization initiator may also function as a thermal radical polymerization initiator, and the thermal radical polymerization initiator may also function as an active energy ray radical polymerization initiator.

[0188] The radical polymerization initiator may be commercially available. Examples of commercially available radical polymerization initiators include the Omnirad series manufactured by IGM Resins BV and the Percure series manufactured by NOF Corporation. These may be used alone or in combination of two or more types.

[0189] The polymerization initiator is preferably an active energy ray radical polymerization initiator, more preferably a photopolymerization initiator. The blending ratio and blending timing of the polymerization initiator are appropriately set depending on the purpose and application.

[0190] (3-8) Acrylic resin raw material formulation The acrylic resin raw material may be in the form of a mixture containing the radical polymerizable monomer and the polymerization initiator. The acrylic resin raw material may also contain a known organic solvent. Preferably, the acrylic resin raw material does not contain an organic solvent and is composed of the radical polymerizable monomer and the polymerization initiator.

[0191] (4) Form of the curable composition The curable composition contains, for example, a plasticizer and a curable compound as described above. Preferably, the curable composition contains a plasticizer and a polyurethane resin raw material and / or an acrylic resin raw material as the curable compound. More preferably, the curable composition contains a plasticizer and a polyurethane resin raw material, or a plasticizer and an acrylic resin raw material.

[0192] The blending ratio of the plasticizer and the curable compound is not particularly limited and is appropriately set depending on the purpose and application. For example, the plasticizer is, for example, 1 part by mass (phr) or more, preferably 5 parts by mass (phr) or more, relative to 100 parts by mass of the solid content of the curable compound. Furthermore, the plasticizer is, for example, 70 parts by mass (phr) or less, preferably 50 parts by mass (phr) or less, relative to 100 parts by mass of the solid content of the curable compound.

[0193] Also, for example, a plasticizer and a curable compound of The plasticizer is, for example, 1% by mass or more, preferably 3% by mass or more, based on the total amount (based on the solid content). of The plasticizer content is, for example, 50 mass % or less, or preferably 35 mass % or less, based on the total amount (solid content).

[0194] The content of the curable compound is, for example, 50% by mass or more, preferably 65% ​​by mass or more, based on the total amount (solid content) of the plasticizer and the curable compound, and is, for example, 99% by mass or less, preferably 97% by mass or less, based on the total amount (solid content) of the plasticizer and the curable compound.

[0195] The form in which the plasticizer is contained is not particularly limited. For example, when the curable compound is a two-component curing polyurethane resin, the plasticizer may be added to the curing agent (polyisocyanate) of the two-component curing polyurethane resin. The plasticizer may also be added to the base agent (polyol) of the two-component curing polyurethane resin. The plasticizer may also be added to both the base agent and the curing agent of the two-component curing polyurethane resin.

[0196] The plasticizer may be prepared separately from the base agent and curing agent of the two-component curing polyurethane resin. When the plasticizer is prepared separately, the plasticizer may be added simultaneously with the base agent and curing agent when they are mixed, or may be added to the mixture after the base agent and curing agent are mixed.

[0197] Furthermore, for example, when the curable compound is an acrylic resin raw material, the plasticizer may be mixed in advance with the radical polymerizable monomer. Alternatively, the plasticizer may be mixed in advance with the polymerization initiator. Alternatively, the plasticizer may be added simultaneously with the mixing of the radical polymerizable monomer and the polymerization initiator, or may be added to the mixture after the mixing of the radical polymerizable monomer and the polymerization initiator.

[0198] (5) Subsidiary ingredients The curable composition may contain additives as minor components as needed. The minor components are components whose content relative to the total content is a predetermined value or less. The content ratio of the minor components relative to the total content is, for example, 10% by mass or less. In other words, the proportion of the additives relative to the total solid content of the curable composition is 10% by mass or less.

[0199] Examples of additives include ultraviolet absorbers (UV absorbers), light stabilizers (light stabilizers), and antioxidants. Further examples of additives include heat stabilizers, crosslinkers, silane coupling agents, antifoaming agents, leveling agents, mildew inhibitors, rust inhibitors, matting agents, flame retardants, thixotropic agents, tackifiers, thickeners, lubricants, antistatic agents, surfactants, reaction retarders, hydrolysis inhibitors, dyes, inorganic pigments, organic pigments, anti-tack agents, inorganic fillers, and organic fillers. These may be used alone or in combination of two or more. The amount and timing of the additives added are appropriately determined depending on the purpose and application.

[0200] From the viewpoint of weather resistance of the cured product (described later), the additives preferably include an ultraviolet absorber (UV absorber), a light stabilizer (light stabilizer), and an antioxidant. That is, the curable composition preferably contains an ultraviolet absorber, a light stabilizer, and an antioxidant. Agent and antioxidants. From the viewpoint of weather resistance of the cured product (described later), additives (ultraviolet absorbers, light-resistant stabilizers) Agent and at least one additive selected from the group consisting of antioxidants) is, for example, 1 × 10 -6 Parts by mass (ppm) or more, preferably 10 x 10 -6 Parts by mass (ppm) or more, more preferably 100 × 10 -6 In addition, from the viewpoint of cost reduction, additives (ultraviolet absorbers, light-resistant stabilizers) Agent and at least one additive selected from the group consisting of antioxidants) is, for example, 100,000 × 10 -6 Parts by mass (ppm) or less, preferably 10000 x 10 -6 parts by mass (ppm) or less, more preferably 1000 x 10 -6 Parts by mass (ppm) or less.

[0201] The ultraviolet absorber is not particularly limited, and examples thereof include known ultraviolet absorbers (for example, those described in the ADEKA catalog and the CLARIANT catalog). More specific examples of ultraviolet absorbers include benzotriazole-based ultraviolet absorbers, benzophenone-based ultraviolet absorbers, benzylidene-based ultraviolet absorbers, and triazine-based ultraviolet absorbers. These are used alone or in combination of two or more. From the viewpoint of weather resistance of the cured product (described later), a preferred ultraviolet absorber is a benzotriazole-based ultraviolet absorber. The blending ratio of the ultraviolet absorber is, for example, 1×10 relative to 1 part by mass of the above-mentioned curable composition. -6 Parts by mass (ppm) or more, preferably 10 x 10 -6 Parts by mass (ppm) or more, more preferably 100 × 10 -6 From the viewpoint of cost reduction, the blending ratio of the ultraviolet absorber is, for example, 100,000×10 -6 Parts by mass (ppm) or less, preferably 10000 x 10-6 parts by mass (ppm) or less, more preferably 1000 x 10 -6 Parts by mass (ppm) or less.

[0202] The light resistance stabilizer is not particularly limited, and examples thereof include known light resistance stabilizers (for example, those described in the catalogue of ADEKA). More specific examples of the light resistance stabilizer include hindered amine (HALS) light resistance stabilizers and benzoate light resistance stabilizers. These are used alone or in combination of two or more. From the viewpoint of the weather resistance of the cured product (described later), the light resistance stabilizer is preferably a hindered amine (HALS) light resistance stabilizer. The blending ratio of the light resistance stabilizer relative to 1 part by mass of the above-mentioned curable composition is, for example, 1 x 10 -6 Parts by mass (ppm) or more, preferably 10 x 10 -6 Parts by mass (ppm) or more, more preferably 100 × 10 -6 From the viewpoint of cost reduction, the blending ratio of the light resistance stabilizer is, for example, 100,000×10 parts by mass (ppm) or more relative to 1 part by mass of the curable composition. -6 Parts by mass (ppm) or less, preferably 10000 x 10 -6 parts by mass (ppm) or less, more preferably 1000 x 10 -6 Parts by mass (ppm) or less.

[0203] The antioxidant is not particularly limited, and examples thereof include known antioxidants (for example, those listed in the catalogue of ADEKA). More specific examples of the antioxidant include phenol-based antioxidants, phosphorus-based antioxidants, and thiophene-based antioxidants. These are used alone or in combination of two or more. From the viewpoint of the weather resistance of the cured product (described later), a phenol-based antioxidant is preferably used as the antioxidant. The blending ratio of the antioxidant is, for example, 1×10 with respect to 1 part by mass of the above-mentioned curable composition. -6 Parts by mass (ppm) or more, preferably 10 x 10 -6 Parts by mass (ppm) or more, more preferably 100 × 10 -6From the viewpoint of cost reduction, the blending ratio of the antioxidant is, for example, 100,000×10 parts by mass (ppm) or more relative to 1 part by mass of the curable composition. -6 Parts by mass (ppm) or less, preferably 10000 x 10 -6 parts by mass (ppm) or less, more preferably 1000 x 10 -6 Parts by mass (ppm) or less.

[0204] (6)Applications The curable composition is suitably used in various industrial fields. Examples of applications of the curable composition include coating agents, paints, and adhesives. A preferred application of the curable composition is an adhesive.

[0205] The adhesive is an uncured curable composition that, when cured, forms a cured adhesive product (a cured product described below) that bonds adherends.

[0206] The curable composition can provide a cured product having an excellent refractive index and excellent flexibility. Therefore, the curable composition is suitable for use as an optical curable composition. Examples of applications of the optical curable composition include optical coating agents, optical paints, and optical adhesives.

[0207] 4.Cured product (1) Main component The cured product contains the above-mentioned plasticizer and cured resin as main components. The main component is a component whose content relative to the total is equal to or greater than a predetermined value. The content ratio of the main component relative to the total is, for example, 90% by mass or more. In other words, the total solid content of the plasticizer and cured resin is 90% by mass or more relative to the total solid content of the cured product.

[0208] The cured product is formed by curing the curable composition by a known method. The method for curing the curable composition is appropriately selected depending on the type of curable compound.

[0209] (2) Cured resin The cured resin contains, for example, a cured product of the above-mentioned curable compound, and preferably consists of a cured product of the above-mentioned curable compound.

[0210] More specifically, cured resins include cured polyurethane resins, cured polyolefin resins, cured polyamine resins, cured amide resins, cured urea resins, cured phenolic resins, cured epoxy resins, cured acrylic resins, cured melamine resins, and cured alkyd resins, which may be used alone or in combination of two or more.

[0211] The cured resin preferably includes a cured polyurethane resin and a cured acrylic resin.

[0212] Examples of cured polyurethane resins include cured products of the polyurethane resin raw materials described above. More specifically, cured polyurethane resins include reaction products of the base agent containing the polyol described above and the curing agent containing the polyisocyanate described above. Such cured resins can provide cured products that have both a superior refractive index and superior flexibility. More specifically, if the cured resin includes a cured polyurethane resin (a reaction product of the base agent containing the acrylic polyol described above and the curing agent containing the polyisocyanate described above), a cured product that satisfies the physical properties (refractive index and flexibility) described below can be more easily obtained.

[0213] Examples of cured acrylic resins include cured products of the above-mentioned acrylic resin raw materials. More specifically, examples of cured acrylic resins include reaction products obtained by radical polymerization of the above-mentioned radically polymerizable monomers. The method for obtaining the cured acrylic resin is not particularly limited. For example, when an active energy ray radical polymerization initiator is used, the acrylic resin raw material is irradiated with active energy rays having a predetermined wavelength. When a thermal radical polymerization initiator is used, the acrylic resin raw material is heated to a predetermined temperature. This activates the polymerization initiator, causing the radically polymerizable monomers to undergo a radical polymerization reaction, thereby obtaining a cured acrylic resin. In particular, when the cured resin contains a cured acrylic resin (a radical polymerization product of the above-mentioned monomer components), a cured product having excellent flexibility and an especially excellent refractive index can be obtained.

[0214] (3) Subcomponents The cured product may contain the additives described above as minor components, as needed. The minor components are components whose content relative to the total is equal to or less than a predetermined value. The content ratio of the minor components relative to the total is, for example, 10% by mass or less. In other words, the proportion of the additives relative to the total solid content of the cured product is 10% by mass or less.

[0215] From the viewpoint of weather resistance of the cured product, the additives preferably include an ultraviolet absorber (UV absorber), a light stabilizer (light stabilizer), and an antioxidant. Agent and antioxidants. From the viewpoint of weather resistance of the cured product, additives (ultraviolet absorbers, light-resistant stabilizers) Agent and at least one additive selected from the group consisting of antioxidants) is, for example, 1 × 10 -6 Parts by mass (ppm) or more, preferably 10 x 10 -6 Parts by mass (ppm) or more, more preferably 100 × 10 -6 In addition, from the viewpoint of cost reduction, additives (ultraviolet absorbers, light-resistant stabilizers) Agentand at least one additive selected from the group consisting of antioxidants) is, for example, 100,000 × 10 -6 Parts by mass (ppm) or less, preferably 10000 x 10 -6 parts by mass (ppm) or less, more preferably 1000 x 10 -6 Parts by mass (ppm) or less.

[0216] The ultraviolet absorber is not particularly limited, and examples thereof include known ultraviolet absorbers (for example, those listed in the ADEKA catalog). More specific examples of ultraviolet absorbers include benzotriazole-based ultraviolet absorbers, benzophenone-based ultraviolet absorbers, benzylidene-based ultraviolet absorbers, and triazine-based ultraviolet absorbers. These are used alone or in combination of two or more. From the viewpoint of weather resistance of the cured product, the ultraviolet absorber is preferably a benzotriazole-based ultraviolet absorber. The blending ratio of the ultraviolet absorber is, for example, 1×10 per 1 part by mass of the above-mentioned cured product. -6 Parts by mass (ppm) or more, preferably 10 x 10 -6 Parts by mass (ppm) or more, more preferably 100 × 10 -6 From the viewpoint of cost reduction, the blending ratio of the ultraviolet absorber is, for example, 100,000×10 -6 Parts by mass (ppm) or less, preferably 10000 x 10 -6 parts by mass (ppm) or less, more preferably 1000 x 10 -6 Parts by mass (ppm) or less.

[0217] The light resistance stabilizer (light stabilizer) is not particularly limited, and examples thereof include known light resistance stabilizers (for example, those described in the ADEKA catalog). More specific examples of light resistance stabilizers include hindered amine (HALS) light resistance stabilizers and benzoate light resistance stabilizers. These are used alone or in combination of two or more. From the viewpoint of weather resistance of the cured product, the light resistance stabilizer is preferably a hindered amine (HALS) light resistance stabilizer. The blending ratio of the light resistance stabilizer is, for example, 1×10 per 1 part by mass of the above-mentioned cured product. -6 Parts by mass (ppm) or more, preferably 10 x 10 -6 Parts by mass (ppm) or more, more preferably 100 × 10 -6 From the viewpoint of cost reduction, the blending ratio of the light resistance stabilizer is, for example, 100,000×10 parts by mass (ppm) or more relative to 1 part by mass of the cured product. -6 Parts by mass (ppm) or less, preferably 10000 x 10 -6 parts by mass (ppm) or less, more preferably 1000 x 10 -6 Parts by mass (ppm) or less.

[0218] The antioxidant is not particularly limited, and examples thereof include known antioxidants (for example, those listed in the catalogue of ADEKA). More specific examples of the antioxidant include phenol-based antioxidants, phosphorus-based antioxidants, and thiophene-based antioxidants. These are used alone or in combination of two or more. From the viewpoint of weather resistance of the cured product, a phenol-based antioxidant is preferably used as the antioxidant. The blending ratio of the antioxidant is, for example, 1×10 per part by mass of the above-mentioned cured product. -6 Parts by mass (ppm) or more, preferably 10 x 10 -6 Parts by mass (ppm) or more, more preferably 100 × 10 -6 From the viewpoint of cost reduction, the blending ratio of the antioxidant is, for example, 100,000×10 parts by mass (ppm) or more relative to 1 part by mass of the cured product. -6 Parts by mass (ppm) or less, preferably 10000 x 10 -6 parts by mass (ppm) or less, more preferably 1000 x 10 -6Parts by mass (ppm) or less.

[0219] (4) Physical properties The cured product contains the compound, and therefore has both an excellent refractive index and excellent flexibility.

[0220] The refractive index of the cured product is relatively high. The refractive index of the cured product is, for example, 1.45 or more, preferably 1.50 or more, more preferably 1.55 or more, even more preferably 1.60 or more, and particularly preferably 1.61 or more. The refractive index of the cured product is, for example, 1.80 or less, preferably 1.70 or less. The refractive index is measured in accordance with the examples described below.

[0221] The tensile storage modulus (E') of the cured product at 25°C is relatively low. The tensile storage modulus (E') of the cured product at 25°C is, for example, 1000 MPa or less, preferably 800 MPa or less, more preferably 500 MPa or less, even more preferably 300 MPa or less, even more preferably 200 MPa or less, still more preferably 100 MPa or less, and particularly preferably 50 MPa or less. The tensile storage modulus (E') of the cured product at 25°C is, for example, 1 MPa or more. The tensile storage modulus (E') is measured in accordance with the examples described later.

[0222] (5)Applications The cured product is suitably used in various industrial fields. Examples of uses of the cured product include resin molded products, films, and pressure-sensitive adhesives. A preferred use of the cured product is pressure-sensitive adhesives.

[0223] The adhesive is a cured curable composition. For example, the adhesive is a cured product of a curable composition containing a polyurethane resin raw material and / or an acrylic resin raw material (preferably an acrylic resin raw material) as a curable compound. The adhesive has a relatively low glass transition temperature (0°C or lower) and has adhesiveness (tackiness).

[0224] The cured product has an excellent refractive index and flexibility, and is therefore suitable for use as an optical resin, for example, in optical lenses, optical films, and optical pressure-sensitive adhesives.

[0225] The curable composition, adhesive, and pressure-sensitive adhesive each contain the plasticizer, and therefore, such a curable composition can provide a cured product that has both a refractive index and flexibility. [Example]

[0226] Next, the present invention will be described based on examples and comparative examples, but the present invention is not limited thereto. Note that "parts" and "%" are by mass unless otherwise specified. Furthermore, specific numerical values ​​such as blending ratios (content ratios), physical property values, and parameters used in the following description can be substituted with the corresponding upper limit values ​​(numeric values ​​defined as "equal to or less than") or lower limit values ​​(numeric values ​​defined as "equal to or more than" or "exceeding") of the blending ratios (content ratios), physical property values, and parameters described in the above "Modes for Carrying Out the Invention."

[0227] 1. Synthesis of plasticizer Example 1 (Bn-GST) 4-Benzylthiomethyl-1,8-bisbenzylthio-3,6-dithiaoctane (Bn-GST) was synthesized by the following method.

[0228] First, 40.5 g (595.0 mmol) of sodium ethoxide and 300 mL of ethanol were placed in a four-neck flask equipped with a stirrer, a thermometer, a nitrogen inlet line, and a dropping funnel, and the mixture was stirred to obtain a sodium ethoxide solution.

[0229] Next, 50.0 g (191.9 mmol) of 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane (GST) was slowly added to the sodium ethoxide solution with stirring, thereby obtaining a reaction solution of sodium ethoxide and GST.

[0230] The reaction solution was then cooled in an ice bath. Then, while maintaining the internal temperature of the reaction solution at 10°C or less, 101.8g of benzyl bromide was added to the reaction solution. g (595.0 mmol) was added dropwise.

[0231] The equivalent ratio of bromine atoms in benzyl bromide to mercapto groups in GST (bromine atoms / mercapto groups) was 1.03.

[0232] The ice bath was then removed from the reaction solution, allowing the temperature of the reaction solution to reach room temperature, and the reaction solution was stirred overnight.

[0233] Then, 300 mL of water was added to the reaction solution. Furthermore, dilute hydrochloric acid was added to the reaction solution. This adjusted the pH of the reaction solution to 6.0 or less. The pH was confirmed using pH test paper.

[0234] Thereafter, 500 mL of dichloromethane was added to the reaction solution. Then, these mixed solutions were separated, and the organic phase was taken out. Next, the organic phase was concentrated using an evaporator. This resulted in a concentrated reaction solution.

[0235] The concentrate (crude product) was diluted with 100 mL of dichloromethane to obtain a diluted solution. The diluted solution was passed through 100 mL of silica gel. 300 mL of dichloromethane was used to drain the diluted solution. The diluted solution was then concentrated using an evaporator. This yielded 4-benzylthiomethyl-1,8-bisbenzylthio-3,6-dithiaoctane (Bn-GST) as the reaction product.

[0236] The Bn-GST was a pale yellow, transparent liquid. The yield of Bn-GST was 84.2 g. The viscosity of Bn-GST (at 25°C) was 500 mPa·s. The refractive index (nD) of Bn-GST was 1.63.

[0237] In addition, Bn-GST is as follows: 1 The compound was identified by H-NMR (400 MHz, CDCl3).

[0238] 1 H-NMR (400 MHz, CDCl3): δ7.19-7.37(m,15H) δ3.70-3.78(m,6H) δ2.49-2.85(m,13H)

[0239] Example 2 (Bz-GST) 4-Benzoylthiomethyl-1,8-bisbenzoylthio-3,6-dithiaoctane (Bz-GST) was synthesized by the following method.

[0240] First, 30.0 g (115.2 mmol) of 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane (GST) was placed in a four-neck flask equipped with a stirrer, a thermometer, a nitrogen inlet line, and a dropping funnel.

[0241] Next, 100 mL of dichloromethane was added to the flask, thereby obtaining a solution of GST.

[0242] Next, 38.5 g (380.0 mmol) of triethylamine was slowly added to the GST solution while stirring, thereby obtaining a reaction solution of triethylamine and GST.

[0243] The reaction solution was then cooled in an ice bath, and 53.4 g (380.0 mmol) of benzoyl chloride was added dropwise to the reaction solution while maintaining the internal temperature of the reaction solution at 10° C. or lower.

[0244] The equivalent ratio of chlorine atoms in benzoyl chloride to mercapto groups in GST (chlorine atoms / mercapto groups) was 1.10.

[0245] The ice bath was then removed from the reaction solution, allowing the temperature of the reaction solution to reach room temperature, and the reaction solution was stirred overnight.

[0246] Thereafter, 300 mL of water and 200 mL of dichloromethane were added to the reaction solution. Then, these mixtures were separated, and the organic phase was separated. Next, the organic phase was washed with dilute hydrochloric acid. Furthermore, the organic phase was washed with saturated aqueous sodium bicarbonate solution. Thereafter, the organic phase was concentrated using an evaporator. This resulted in a concentrated reaction solution.

[0247] The concentrate (crude product) was diluted with 100 mL of dichloromethane to obtain a diluted solution. The diluted solution was passed through 100 mL of silica gel. 300 mL of dichloromethane was used to drain the diluted solution. The diluted solution was then concentrated using an evaporator. This yielded 4-benzoylthiomethyl-1,8-bisbenzoylthio-3,6-dithiaoctane (Bz-GST) as the reaction product.

[0248] Bz-GST was a colorless, transparent liquid. The yield of Bz-GST was 63.2 g. The viscosity of Bz-GST (25°C) was 5000 mPa·s. The refractive index (nD) of Bz-GST was 1.65.

[0249] In addition, Bz-GST is as follows: 1 The compound was identified by H-NMR (400 MHz, CDCl3).

[0250] 1 H-NMR (400 MHz, CDCl3): δ7.89-8.01(m,6H) δ7.51-7.61(m,3H) δ7.37-7.48(m,6H) δ2.79-3.59(m,13H)

[0251] Example 3 (Ac-GST) 4-Acetylthiomethyl-1,8-bisacetylthio-3,6-dithiaoctane (Ac-GST) was synthesized by the following method.

[0252] First, 5.00 g (19.2 mmol) of 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane (GST) was placed in a four-neck flask equipped with a stirrer, a thermometer, a nitrogen inlet line, and a dropping funnel.

[0253] Next, 20 mL of dichloromethane was added to the flask, thereby obtaining a solution of GST.

[0254] Next, 6.41 g (63.3 mmol) of triethylamine was slowly added to the GST solution while stirring, thereby obtaining a reaction solution of triethylamine and GST.

[0255] The reaction solution was then cooled in an ice bath. Then, while maintaining the internal temperature of the reaction solution at 10°C or less, 6.47g of acetic anhydride was added to the reaction solution. g (63.3 mmol) was added dropwise.

[0256] The equivalent ratio of the carboxyl groups of acetic anhydride to the mercapto groups in GST (carboxyl groups / mercapto groups) was 2.20.

[0257] The ice bath was then removed from the reaction solution, allowing the temperature of the reaction solution to reach room temperature, and the reaction solution was stirred overnight.

[0258] Then, 30 mL of water and 20 mL of dichloromethane were added to the reaction solution. Then, the mixture was separated and the organic phase was taken out. Next, the organic phase was washed with dilute hydrochloric acid. The organic phase was washed with a saturated aqueous solution of sodium bicarbonate and then concentrated using an evaporator to obtain a concentrated reaction solution.

[0259] The concentrate (crude product) was diluted with 10 mL of dichloromethane to obtain a diluted solution. The diluted solution was passed through 10 mL of silica gel. 30 mL of dichloromethane was used to drain the diluted solution. The diluted solution was then concentrated using an evaporator. This yielded 4-acetylthiomethyl-1,8-bisacetylthio-3,6-dithiaoctane (Ac-GST) as the reaction product.

[0260] Ac-GST was a colorless, transparent liquid. The yield of Ac-GST was 7.21 g. The viscosity of Ac-GST (at 25°C) was 200 mPa·s. The refractive index (nD) of Ac-GST was 1.58.

[0261] In addition, Ac-GST is as follows: 1 The compound was identified by H-NMR (400 MHz, CDCl3).

[0262] 1 H-NMR (400 MHz, CDCl3): δ2.71-3.34(m,13H) δ2.33-2.38(m,9H)

[0263] Example 4 (PA-GST) 4-Phenylacetylthiomethyl-1,8-bisphenylacetylthio-3,6-dithiaoctane (PA-GST) was synthesized by the following method.

[0264] First, 50.0 g (191.9 mmol) of 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane (GST) was placed in a four-neck flask equipped with a stirrer, a thermometer, a nitrogen inlet line, and a dropping funnel.

[0265] Next, 250 g of toluene was added to the flask, thereby obtaining a solution of GST.

[0266] Next, 61.8 g (610.3 mmol) of triethylamine was slowly added to the GST solution while stirring, thereby obtaining a reaction solution of triethylamine and GST.

[0267] The reaction solution was then cooled in an ice bath, and 91.7 g (593.1 mmol) of phenylacetyl chloride was added dropwise to the reaction solution while maintaining the internal temperature of the reaction solution at 15° C. or lower.

[0268] The equivalent ratio of chlorine atoms in phenylacetyl chloride to mercapto groups in GST (chlorine atoms / mercapto groups) was 1.03.

[0269] After the dropwise addition was completed, the reaction solution was stirred for 2 hours while maintaining the internal temperature of the reaction solution at 15°C or below.

[0270] Then, 550 g of a 10% aqueous solution of sodium chloride was added to the reaction solution. Then, the mixture was separated and the organic phase was separated. The organic phase was then washed with 500 mL of 1N diluted hydrochloric acid, followed by 500 mL of saturated aqueous sodium bicarbonate solution, and then with 500 mL of pure water.

[0271] The washings were passed through activated alumina (300 mesh, basic, for chromatography), and 120 g of toluene was used to flush out the reaction product remaining in the alumina.

[0272] After the liquid was passed through the washings, anhydrous sodium sulfate was added to the washings and stirred to remove any remaining water. The sodium sulfate was filtered off using pleated filter paper to obtain a toluene-diluted product. The diluted solution was then concentrated using an evaporator. This yielded the reaction product, 4-phenylacetylthiomethyl-1,8-bisphenylacetylthio-3,6-dithiaoctane (PA-GST).

[0273] PA-GST was a pale yellow, transparent liquid. The yield of PA-GST was 105.2 g. The viscosity of PA-GST (at 25°C) was 1100 mPa·s. The refractive index (nD) of PA-GST was 1.62.

[0274] The PA-GST is as follows: 1 The compound was identified by H-NMR (400 MHz, CDCl3).

[0275] 1 H-NMR (400 MHz, CDCl3): δ7.21-7.37(m,15H) δ3.80-3.84(m,6H) δ2.64-3.25(m,13H)

[0276] Example 5 (PP-GST) 4-(3-phenylpropionyl)thiomethyl-1,8-bis(3-phenylpropionyl)thio-3,6-dithiaoctane (PP-GST) was synthesized by the following method.

[0277] First, 50.0 g (191.9 mmol) of 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane (GST) was placed in a four-neck flask equipped with a stirrer, a thermometer, a nitrogen inlet line, and a dropping funnel.

[0278] Next, 250 g of toluene was added to the flask, thereby obtaining a solution of GST.

[0279] Next, 61.8 g (610.3 mmol) of triethylamine was slowly added to the GST solution while stirring, thereby obtaining a reaction solution of triethylamine and GST.

[0280] The reaction solution was then cooled in an ice bath, and 100.0 g (593.1 mmol) of 3-phenylpropionyl chloride was added dropwise to the reaction solution while maintaining the internal temperature of the reaction solution at 15° C. or lower.

[0281] The equivalent ratio of chlorine atoms in 3-phenylpropionyl chloride to mercapto groups in GST (chlorine atoms / mercapto groups) was 1.03.

[0282] After the dropwise addition was completed, the reaction solution was stirred for 2 hours while maintaining the internal temperature of the reaction solution at 15°C or below.

[0283] Then, 550 g of a 10% aqueous solution of sodium chloride was added to the reaction solution. Then, the mixture was separated and the organic phase was separated. The organic phase was then washed with 500 mL of 1N diluted hydrochloric acid, followed by 500 mL of saturated aqueous sodium bicarbonate solution, and then with 500 mL of pure water.

[0284] The washings were passed through activated alumina (300 mesh, basic, for chromatography), and 120 g of toluene was used to flush out the reaction product remaining in the alumina.

[0285] After the washings were passed through the column, anhydrous sodium sulfate was added to the washings and stirred to remove any remaining water. The sodium sulfate was filtered off using pleated filter paper to obtain a toluene-diluted product. The diluted solution was then concentrated using an evaporator. This yielded the reaction product, 4-(3-phenylpropionyl)thiomethyl-1,8-bis(3-phenylpropionyl)thio-3,6-dithiaoctane (PP-GST).

[0286] PP PP-GST was a pale yellow, transparent liquid. The yield of PP-GST was 119.0 g. The viscosity of PP-GST (at 25°C) was 400 mPa·s. The refractive index (nD) of PP-GST was 1.60.

[0287] PP-GST is as follows: 1 The compound was identified by H-NMR (400 MHz, CDCl3).

[0288] 1 H-NMR (400 MHz, CDCl3): δ7.13-7.33(m,15H) δ2.66-3.29(m,25H)

[0289] Example 6 (Bz-FSH) 5,7-Bis(benzoylmercaptomethyl)-1,11-bis(benzoylmercapto)-3,6,9-trithiaundecane (Bz-FSH) was synthesized by the following method.

[0290] First, 50.0 g (136.4 mmol) of 5,7-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane (FSH) was placed in a four-neck flask equipped with a stirrer, a thermometer, a nitrogen inlet line, and a dropping funnel.

[0291] Next, 500 g of toluene was added to the flask, thereby obtaining a solution of FSH.

[0292] Next, 42.8 g (422.7 mmol) of triethylamine was slowly added to the FSH solution while stirring, thereby obtaining a reaction solution of triethylamine and FSH.

[0293] The reaction solution was then cooled in an ice bath, and 59.4 g (422.7 mmol) of benzoyl chloride was added dropwise to the reaction solution while maintaining the internal temperature of the reaction solution at 15° C. or lower.

[0294] The equivalent ratio of chlorine atoms in benzoyl chloride to mercapto groups in FSH (chlorine atoms / mercapto groups) was 1.03.

[0295] After the dropwise addition was completed, the reaction solution was stirred for 2 hours while maintaining the internal temperature of the reaction solution at 15°C or below.

[0296] Then, 550 g of a 10% aqueous solution of sodium chloride was added to the reaction solution. Then, the mixture was separated and the organic phase was separated. The organic phase was then washed with 500 mL of 1N diluted hydrochloric acid, followed by 500 mL of saturated aqueous sodium bicarbonate solution, and then with 500 mL of pure water.

[0297] The washings were passed through activated alumina (300 mesh, basic, for chromatography), and 120 g of toluene was used to flush out the reaction product remaining in the alumina.

[0298] After the washings were passed through the column, anhydrous sodium sulfate was added to the washings and stirred to remove any remaining water. The sodium sulfate was filtered off using pleated filter paper to obtain a toluene-diluted product. The diluted solution was then concentrated using an evaporator. This yielded the reaction product, 5,7-bis(benzoylmercaptomethyl)-1,11-bis(benzoylmercapto)-3,6,9-trithiaundecane (Bz-FSH).

[0299] Bz-FSH was a pale yellow, transparent liquid. The yield of Bz-FSH was 104.8 g. The viscosity of Bz-FSH (at 25°C) was 8000 mPa·s. The refractive index (nD) of Bz-FSH was 1.65.

[0300] In addition, Bz-FSH is as follows: 1 The compound was identified by H-NMR (400 MHz, CDCl3).

[0301] 1 H-NMR (400 MHz, CDCl3): δ7.89-8.01(m,8H) δ7.51-7.61(m,4H) δ7.37-7.48(m,8H) δ2.79-3.59(m,18H)

[0302] 2. Preparing the Curing Agent Preparation Example 1 (Isocyanate Curing Agent) The following commercially available isocyanate curing agents were prepared: D-110N: Trade name: Takenate D-110N, xylylene diisocyanate trimethylolpropane (TMP) adduct, ethyl acetate solution, solids concentration 75% by mass, isocyanate group content 11.5% by mass, manufactured by Mitsui Chemicals, Inc.

[0303] 3. Synthesis of the main agent Preparation Example 2 (Acrylic Polyol 1) Acrylic polyol 1 was synthesized by the following method.

[0304] First, the mixer 、 A four-neck flask equipped with a thermometer and a nitrogen inlet line was charged with 120 parts by mass of a polymerization solvent (toluene) and 40 parts by mass of ethyl acetate. Then, while blowing nitrogen into the flask, the internal temperature of the flask was heated to 80±2°C.

[0305] Meanwhile, the following ingredients were placed in a brown bottle and mixed to obtain a mixed solution. Toluene 40 parts by mass NMT-A (1-naphthyl methyl acrylate) 80.0 parts by mass POB-A (m-phenoxybenzyl acrylate) 110 parts by mass HEA (2-hydroxyethyl acrylate) 10.0 parts by mass PB-O (t-butylperoxy-2-ethylhexanoate) 2.0 parts by mass

[0306] The mixture was added dropwise to the flask continuously for 5 hours, after which the contents of the flask were kept at 80±2°C for 1 hour.

[0307] Next, 0.4 parts by mass of PB-O was added to the flask twice, every hour. This removed any unreacted components (residual monomers). After adding PB-O twice, the contents of the flask were further kept at 80±2°C for 2 hours. This gave acrylic polyol 1.

[0308] Acrylic polyol 1 was a pale yellow, transparent liquid. The solid content (non-volatile content) concentration of acrylic polyol 1 was 49.8 mass %. The hydroxyl value (based on the solid content) of acrylic polyol 1 was 22.3 mg KOH / g.

[0309] Preparation Example 3 (Acrylic Polyol 2) The recipe of the mixed solution was changed as follows: Acrylic polyol 2 was synthesized in the same manner as in Preparative Example 2. Toluene 40 parts by mass NMT-A (1-naphthyl methyl acrylate) 40.0 parts by mass POB-A (m-phenoxybenzyl acrylate) 150 parts by mass HEA (2-hydroxyethyl acrylate) 10.0 parts by mass PB-O (t-butylperoxy-2-ethylhexanoate) 2.0 parts by mass

[0310] Acrylic polyol 2 was a yellow, transparent liquid. The solid content (non-volatile content) concentration of acrylic polyol 2 was 50.4 mass %. The hydroxyl value (based on the solid content) of acrylic polyol 2 was 22.4 mg KOH / g.

[0311] Preparation Example 4 (Acrylic Polyol 3) The recipe of the mixed solution was changed as follows: Acrylic polyol 3 was synthesized in the same manner as in Preparative Example 2. Toluene 40 parts by mass POB-A (m-phenoxybenzyl acrylate) 190.0 parts by mass HEA (2-hydroxyethyl acrylate) 10.0 parts by mass PB-O (t-butylperoxy-2-ethylhexanoate) 2.0 parts by mass

[0312] Acrylic polyol 3 was a yellow, transparent liquid. The solid content (non-volatile content) concentration of acrylic polyol 3 was 51.0 mass %. The hydroxyl value (based on the solid content) of acrylic polyol 3 was 22.4 mg KOH / g.

[0313] Preparation Example 5 (Acrylic Polyol 4) As acrylic polyol 4, the following commercially available product was prepared.

[0314] SG-70L: Product name: Teisan Resin SG-70L, carboxyl group-containing acrylic polyol, solids concentration 12.5% ​​by mass, viscosity 1600 mPa·s, total acid value and hydroxyl value 5 mg KOH / g, manufactured by Nagase ChemteX Corporation

[0315] 4. Polyurethane resin production Examples 7 to 20 and Comparative Examples 1 to 5 A base agent (curing base agent), a curing agent, and a plasticizer were prepared according to the formulations shown in Tables 1 and 2. These sets were used as curable compositions. For comparison, dioctyl phthalate (DOP) was also prepared as a plasticizer.

[0316] The base agent and curing agent were mixed so that the equivalent ratio would be the value shown in Tables 1 and 2. When the base agent is acrylic polyols 1 to 3, the equivalent ratio indicates the ratio of hydroxyl groups in the base agent to isocyanate groups in the curing agent (OH / NCO).

[0317] Furthermore, when the base resin is acrylic polyol 4 (carboxy group-containing acrylic polyol), the equivalent ratio indicates the ratio of the total amount of hydroxyl groups and carboxy groups in the base resin to the isocyanate groups in the curing agent (OH+COOH / NCO).

[0318] Next, a plasticizer was added to the mixture of the base agent and curing agent, and the mixture was mixed. The amount of plasticizer added was adjusted according to the information in Tables 1 and 2. In Tables 1 and 2, the blending ratio (phr) of the plasticizer indicates the parts by mass of the plasticizer relative to 100 parts by mass of the total solid content of the mixture of the base agent and curing agent.

[0319] As a result, a mixed solution containing the base material, curing agent, and plasticizer was obtained. Next, the mixed solution was applied to the surface of a polypropylene (PP) substrate. The amount of coating was adjusted so that the thickness of the coating film was 200 μm. The coating film was then heated at 60°C for 2 hours and further aged at 25°C for 7 days. This cured the coating film, yielding a cured product. The cured product was then peeled off from the PP substrate.

[0320] 5. Evaluation (1) Refractive index (nD) The refractive index (nD) of the cured product was measured using an Abbe refractometer (DR-M4, manufactured by Atago Co., Ltd.) at room temperature (20°C) using d-line light (wavelength 587.6 nm).

[0321] (2) Flexibility: Tensile storage modulus (E') The solid viscoelasticity of the cured product was measured under the following conditions, and the tensile storage modulus (E') at 25°C was determined.

[0322] Apparatus: RSA-G2 (manufactured by TA Instruments) Deformation mode; tension mode Temperature range: -50℃~270℃ Temperature rise: 3℃ / min Frequency: 1Hz Environment ;N2 environment

[0323] (3) Glass transition temperature (Tg) The solid viscoelasticity of the cured product was measured under the conditions in (2) above. Then, tanδ (loss tangent, E" / E') was calculated from the tensile storage modulus (E') and the tensile loss modulus (E"). The temperature at which the loss tangent (tanδ) reached its maximum value (peak value) was calculated as the glass transition temperature.

[0324] 6. Additives and their evaluation Examples 21 to 38 Additives were added to the curable compositions of Examples 7 and 10, and the weather resistance of the cured products was confirmed.

[0325] More specifically, a base agent, a curing agent, a plasticizer, and additives were prepared according to the formulations shown in Tables 3 and 4. These sets were used as curable compositions. The base agent and the curing agent were then mixed together so that the equivalent ratio was the value shown in Table 3.

[0326] Next, a plasticizer and an additive were added to the mixture of the base agent and the curing agent, and the mixture was mixed. In Table 3, the blending ratio (phr) of the plasticizer indicates the parts by mass of the plasticizer relative to 100 parts by mass of the total solid content of the mixture of the base agent and the curing agent. In Tables 3 and 4, the blending ratio (ppm) of the additive indicates the mass ratio (ppm) of the additive relative to the total solid content of the base agent, curing agent, plasticizer, and additive (resin solid content (i.e., the total amount of the curable composition and the total amount of the cured product)). In Example 31, no additive was added.

[0327] The types of additives are listed below. LA-24; Trade name: Adeka Stab LA-24, benzotriazole UV absorber, 2-(2H-benzotriazol-2-yl)-4,6-bis(1-methyl-1-phenylethyl)phenol, manufactured by ADEKA LA-29; Trade name: Adeka Stab LA-29, benzotriazole UV absorber, 2-(2H-benzotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)phenol, manufactured by ADEKA LA-32: Trade name: Adeka Stab LA-32, benzotriazole UV absorber, 2-(2H-benzotriazol-2-yl)-p-cresol, manufactured by ADEKA 1413; Trade name: Adeka Stab 1413, benzophenone-based UV absorber, [2-hydroxy-4-(octyloxy)phenyl](phenyl)methanone, manufactured by ADEKA PR-25; Trade name HostavinPR-25, benzylidene UV absorber, dimethyl 2-(4-methoxybenzylidene)propanedioate, manufactured by CLARIANT LA-46; Trade name: Adeka Stab LA-46, triazine UV absorber, 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-[2-(2-ethylhexanoyloxy)ethoxy]phenol, manufactured by ADEKA LA-72: Trade name: Adeka STAB LA-72, HALS light stabilizer, bis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, manufactured by ADEKA AO-60; Trade name Adekastab AO-60, phenolic antioxidant, pentaerythritol tetrakis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propyl] O Neate, manufactured by ADEKA

[0328] As a result, a mixed solution containing the base resin, curing agent, plasticizer, and additives was obtained. The mixed solution was then applied to the surface of a glass substrate (D263T-eco, manufactured by SCHOTT Corporation, 0.21 mm thick, 50 mm × 50 mm). The amount of coating was adjusted so that the thickness of the coating film was 50 μm. The coating film was then heated at 60°C for 2 hours and further aged at 25°C for 7 days. This cured the coating film, yielding a cured product. As a result, a laminate (hereinafter referred to as a glass substrate / cured film laminate) containing a glass substrate and a cured resin film was obtained.

[0329] YI value and b value of each glass substrate / cured film laminate * The yellowing (before weather resistance test) was measured using a COH-7700 (Nippon Denshoku Industries Co., Ltd., spectral color haze meter). The results are shown in Tables 3 and 4.

[0330] Thereafter, each glass substrate / cured film laminate was subjected to a weather resistance test. More specifically, the glass substrate / cured film laminate was exposed to ultraviolet light under the following conditions.

[0331] Light source: Xenon lamp Black panel temperature: 55℃ Humidity: 55% Rain conditions: None Irradiation conditions: 36.5W / m 2 (300-400nm) Filter: Inner / Outer = Right Light / Cica-Quarz Irradiated surface: cured film side Irradiation time: 100 hours

[0332] Then, the YI value and b *The yellowing degree (after weather resistance test) was measured using a COH-7700 (a spectral color haze meter manufactured by Nippon Denshoku Industries Co., Ltd.). The results are shown in Tables 3 and 4.

[0333] 7. Preparation and Evaluation of Cured Acrylic Resins Preparation Example 6 (Acrylic Formulation 1) The following ingredients were placed in a brown bottle and mixed to obtain acrylic formulation 1 (curable compound, acrylic resin raw material 1). TMP-A (trimethicone) roll Propane triacrylate) 40.0 parts by mass 2EHA (2-ethylhexyl acrylate) 60.0 parts by mass Omnirad184 (alkylphenone photopolymerization initiator, 1-hydroxycyclohexyl phenyl ketone) 3.0 parts by mass

[0334] Preparation Example 7 (Acrylic Formulation 2) The following ingredients were placed in a brown bottle and mixed to obtain acrylic formulation 2 (curable compound, acrylic resin raw material 2). TMP-A (trimethylpropane triacrylate) 40.0 parts by mass POB-A (m-phenoxybenzyl acrylate) 60.0 parts by mass Omnirad184 (alkylphenone photopolymerization initiator, 1-hydroxycyclohexyl phenyl ketone) 3.0 parts by mass

[0335] Examples 39 to 46 and Comparative Examples 6 to 7 A plasticizer and a curable compound were blended according to the formulation shown in Table 5 to obtain a curable composition (polymerizable composition).

[0336] Next, in a mold frame made of a 200 μm-thick silicone sheet, the coating film of the polymerizable composition was sandwiched between release PET films (polyethylene terephthalate film, Purex A3100, Toyobo Co., Ltd.). At this time, the release surface of the release PET film was brought into contact with the polymerizable composition. This resulted in a laminate 1 (release PET film / polymerizable composition / release PET film).

[0337] Next, Laminate 1 (release PET film / polymerizable composition / release PET film) was sandwiched between glass substrates (D263T-eco, manufactured by SCHOTT) and fixed with clips. That is, the coating film of the polymerizable composition was sandwiched between the glass substrates and the release PET films, and Laminate 2 (glass substrate / release PET film / polymerizable composition / release PET film / glass substrate) was obtained.

[0338] Thereafter, the polymerizable composition of the laminate 2 was irradiated with active energy rays (wavelength 365 nm, illuminance 400 mW / cm ) using an LED light source (365 nm). 2 , cumulative light intensity 6000mJ / cm 2 ) was irradiated. Furthermore, the laminate 2 was heated at 120°C for 30 minutes in a nitrogen atmosphere. As a result, the polymerizable composition underwent radical polymerization by the active energy rays and heat, and a laminate 3 containing a cured product (glass substrate / release PET film / cured product / release PET film / glass substrate) was obtained.

[0339] The clips and glass substrate were then removed, and the cured product was peeled off from the release PET film. As a result, a cured product was obtained. The refractive index (nD), tensile storage modulus (E'), and glass transition temperature (Tg) of the cured product were measured using the methods described above. The results are shown in Table 5.

[0340] Separately from the above, the polymerizable composition was sandwiched between glass substrates (Eagle-XG, manufactured by Corning) in a mold made of a 50 μm-thick silicone sheet, thereby obtaining Laminate 4 (glass substrate / polymerizable composition / glass substrate).

[0341] Thereafter, the polymerizable composition of the laminate 4 was irradiated with active energy rays (wavelength 365 nm, illuminance 400 mW / cm ) using an LED light source (365 nm). 2 , cumulative light intensity 6000mJ / cm 2) was irradiated. Furthermore, the laminate 4 was heated at 120°C for 30 minutes in a nitrogen atmosphere. As a result, the polymerizable composition underwent radical polymerization by the active energy rays and heat, and a laminate 5 (glass substrate / cured product / glass substrate) containing a cured product was obtained.

[0342] Thereafter, the clips were removed. Then, the laminate 5 (glass substrate / cured product / glass substrate) was measured for the weather resistance YI value and b * The yellowing index (before the weather resistance test) was measured in the same manner as above. Furthermore, the laminate 5 (glass substrate / cured product / glass substrate) was subjected to a weather resistance test in the same manner as above. Thereafter, the YI value and b * The yellowing degree (after the weather resistance test) was measured in the same manner as above. The results are shown in Table 5.

[0343] [Table 1]

[0344] [Table 2]

[0345] [Table 3]

[0346] [Table 4]

[0347] [Table 5]

[0348] The above invention is provided as an exemplary embodiment of the present invention, but it is merely an example and should not be interpreted as being limiting. Modifications of the present invention that are obvious to those skilled in the art are intended to be included in the scope of the following claims. [Industrial Applicability]

[0349] The compound, additive, plasticizer, curable composition, adhesive, cured product and pressure-sensitive adhesive of the present invention are suitably used in the fields of coating agents, paints, adhesives, films and pressure-sensitive adhesives.

Claims

1. An additive comprising a compound represented by the following general formula (1), wherein the general formula (1) is a compound represented by the following general formula (2) or the following general formula (3): General formula (1); 【Chemistry 1】 (In formula (1), A represents an n-valent organic group containing a sulfur atom. n represents an integer of 3 or greater. S represents a sulfur atom. X represents a single bond or a carbonyl group. Xs may be the same or different. R represents an aliphatic hydrocarbon group, an aromatic hydrocarbon group, or an araliphatic hydrocarbon group. Rs may be the same or different.) General formula (2); 【Chemistry 2】 (In formula (2), S, X, and R have the same meanings as S, X, and R in formula (1). In formula (2), the portion surrounded by a dashed line represents the organic group A (n=3) in formula (1).) General formula (3); 【Transformation 3】 (In formula (3), S, X, and R have the same meanings as S, X, and R in formula (1). In formula (3), the portion surrounded by a dashed line represents the organic group A (n=4) in formula (1).)

2. 2. The additive according to claim 1, wherein R represents a methyl group, a phenyl group, or a benzyl group.

3. X represents a carbonyl group, and 2. The additive of claim 1, wherein R represents an araliphatic hydrocarbon group.

4. A plasticizer comprising a compound represented by the following general formula (1), wherein the general formula (1) is a compound represented by the following general formula (2) or the following general formula (3): General formula (1); 【Chemistry 1】 (In formula (1), A represents an n-valent organic group containing a sulfur atom. n represents an integer of 3 or greater. S represents a sulfur atom. X represents a single bond or a carbonyl group. Xs may be the same or different. R represents an aliphatic hydrocarbon group, an aromatic hydrocarbon group, or an araliphatic hydrocarbon group. Rs may be the same or different.) General formula (2); 【Chemistry 2】 (In formula (2), S, X, and R have the same meanings as S, X, and R in formula (1). In formula (2), the portion surrounded by a dashed line represents the organic group A (n=3) in formula (1).) General formula (3); 【Transformation 3】 (In formula (3), S, X, and R have the same meanings as S, X, and R in formula (1). In formula (3), the portion surrounded by a dashed line represents the organic group A (n=4) in formula (1).)

5. 5. The plasticizer according to claim 4, wherein R represents a methyl group, a phenyl group, or a benzyl group.

6. X represents a carbonyl group, and 5. The plasticizer of claim 4, wherein R represents an araliphatic hydrocarbon group.

7. A curable composition comprising the plasticizer of claim 4 and a curable compound.

8. further comprising at least one additive selected from the group consisting of an ultraviolet absorber, a light stabilizer, and an antioxidant; The ratio of the additive to the total amount of the curable composition is 10 × 10 －６ Mass part or more 10,000×10 －６ The curable composition according to claim 7, wherein the amount of the curable composition is equal to or less than parts by weight.

9. An adhesive comprising the curable composition of claim 7.

10. A cured product comprising the plasticizer according to claim 4 and a cured resin.

11. The refractive index is 1.60 or more, and The cured product according to claim 10, having a tensile storage modulus of 100 MPa or less.

12. further comprising at least one additive selected from the group consisting of an ultraviolet absorber, a light stabilizer, and an antioxidant; The ratio of the additives to the total amount of the cured product is 10 × 10 －６ Mass part or more 10,000×10 －６ The cured product according to claim 10, wherein the amount is not more than parts by mass.

13. The cured product according to claim 10 , wherein the cured resin comprises a reaction product of a base resin comprising an acrylic polyol and a curing agent comprising a polyisocyanate.

14. The cured product of claim 10 , wherein the cured resin comprises a cured acrylic resin.

15. A pressure-sensitive adhesive comprising the cured product according to claim 10.

Images