JPH0959382A - Functional group terminated polysulfide compound and its production - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain a function group terminated polysulfide compound in which thiol groups are eliminated, not generating a characteristic odor and useful for various kinds of chemical reactions by adding a functional group having vinylic compound to a thiol group-terminated polysulfide compound. SOLUTION: The functional group-terminated polysulfide compound is produced by reacting compounds of formula I and/or formula II [R<1> H and/or methyl; R<2> is a divalent group; B is the group of hydroxyl, nitrile, carboxyl, amino, ester etc.; A is a divalent or move-valent group having a polysulfide structure which has structural units of the formula: -(R<3> -Sx )- (R<3> is a divalent group; (x) is an integer of 1-5) and has thiol group of the formula: -ϕ-R<4> -S- (R<4> is a divalent group) at the molecular end], e.g. a thiol group-terminated polysulfide compound, with a functional group having vinylic compound of formula III and/or formula IV. The groups R<3> and R<4> preferably contain each a group of the formula: -C2 H4 OCn H2n OC2 H4 (n is an integer of 1-2).

Description

Detailed Description of the Invention

[0001]

TECHNICAL FIELD The present invention relates to a novel functional group-terminated polysulfide compound which can be utilized in various chemical reactions and has no odor peculiar to a thiol group-containing compound, and a method for producing the same.

[0002]

2. Description of the Related Art Polysulfide polymers containing two or more thiol groups in one molecule are widely used in sealing materials, paints, adhesives and the like. Among them, US Patent No. 2,
The polysulfide polymer described in Japanese Patent No. 466,963 easily reacts with various oxidizing agents, epoxide compounds, and isocyanate compounds to have a high molecular weight, and has oil resistance, chemical resistance, gas barrier property, weather resistance, It has been used as a raw material for sealing materials for many years because it yields a rubber elastic body with excellent adhesiveness.

[0003]

However, since such a polysulfide compound has a thiol group at the terminal, its peculiar odor is often a problem, and its industrial application range is limited. In addition, it has been difficult to modify the ends by utilizing the reactivity of functional groups such as hydroxyl groups and amino groups.

Therefore, in order to solve such a problem, conventionally, the end group of the polysulfide compound has been modified with a thiol group.
Attempts have been made to use functional groups other than ruthenium groups.

Japanese Patent Publication No. 40-28797 discloses HO-
Although R'SS (R "SS) hydroxyl-terminated polysulfide compounds represented by _n R'-OH is disclosed, its preparation dichloroethylformal Ma - le and ethylene chlorohydrin polysulfide source - da and weight It is a condensation polymer, and the obtained polymer has a wide molecular weight distribution, and a part of the polymer has a very high molecular weight so that only a high viscosity can be obtained, and a thiol group is also present at the terminal.

Further, British Patent No. 491,309 discloses a method for producing a hydroxyl group-terminated polysulfide compound by etherifying bis-2-hydroxyethyldisulfide in the presence of a strong acid catalyst. . However, in this method, some of the hydroxyl groups in the compound are eliminated as water molecules, so that a compound having a vinyl group end is by-produced, and a pure hydroxyl group-terminated polysulfide compound cannot be obtained.

Further, US Pat. No. 2,469,404 discloses a method for obtaining a hydroxyl group-terminated polysulfide compound by condensation polymerization of bis-2hydroxyethyl disulfide and formalin in the presence of an acid catalyst. Only low molecular weight compounds can be obtained by the method.

Accordingly, an object of the present invention is to provide a high-purity functional group-terminated polysulfide compound having a low odor and a suitable molecular weight and viscosity according to the purpose of use, and a method for producing the same.

[0009]

As a result of earnest research in view of the above object, the present inventors have found that the addition of a vinyl compound having a functional group to a thiol group-terminated polysulfide compound causes the thiol group to be completely removed. The present inventors have found that a functional group-terminated polysulfide compound that disappears and has no peculiar odor can be easily synthesized with high purity, and thus reached the present invention. That is, the functional group-terminated polysulfide compound of the present invention has the general formula (1) and / or (2):

[0010]

[Chemical 6]

[0011]

[Chemical 7] (However, R ¹ is a hydrogen atom and / or a methyl group,
R ² is a divalent group. B is at least one functional group selected from the group consisting of hydroxyl group, nitrile group, carboxyl group, amino group, ester group, isocyanate group, epoxy group and halogen. ), A in the general formulas (1) and (2) is (i)-(R ³ -S _X )-(wherein R ³ is a divalent group, and x is 1 to 5). A thioe represented by (b) to R ⁴ -S- (wherein R ⁴ is a divalent group) at the terminal.
It is characterized by being a divalent or higher valent group having a polysulfide structure having a ter group.

Further, the method for producing a functional group-terminated polysulfide compound according to the present invention is a method in which a thiol group-terminated polysulfide compound is prepared by using a compound represented by the general formula (4) and / or (5):

[0013]

Embedded image

[0014]

Embedded image (However, R ¹ is a hydrogen atom and / or a methyl group,
R ² is a divalent group. B is at least one functional group selected from the group consisting of hydroxyl group, nitrile group, carboxyl group, amino group, ester group, isocyanate group, epoxy group and halogen. ) Is reacted with a vinyl compound having a functional group.

[0015]

BEST MODE FOR CARRYING OUT THE INVENTION The present invention is described in detail below. [1] Structure of functional group-terminated polysulfide compound The functional group-terminated polysulfide compound of the present invention has the general formula (1) and / or (2):

[0016]

Embedded image

[0017]

Embedded image (However, R ¹ is a hydrogen atom and / or a methyl group,
R ² is a divalent group. B is at least one functional group selected from the group consisting of hydroxyl group, nitrile group, carboxyl group, amino group, ester group, isocyanate group, epoxy group and halogen. ), A in the general formulas (1) and (2) is (i)-(R ³ -S _X )-(wherein R ³ is a divalent group, and x is 1 to 5). .. of an integer represented has a structural unit, and to end with), (b) ~~R ⁴ -S- (provided that represented by R ⁴ is a divalent group) thioether -
It is a divalent or higher valent group having a polysulfide structure having a ter group.

The functional group-terminated polysulfide compound of the present invention need only have at least one of the structures of the above general formulas (1) and (2), that is, it contains a divalent group R ² in its skeleton. You don't have to. When R ² is contained, its structure may be linear or branched, and may contain a hetero atom. Further, it may have two or more types of structures.

The divalent group R ² has the general formula (3):

[0020]

[Chemical 12] (However, R ⁵ is an oxyalkylene group having 2 to 10 carbon atoms and / or a polyoxyalkylene group having 2 to 20 oxygen atoms, and the carbon atom at one end is bonded to the functional group B. Those represented by the formula (1) are preferable.
The oxyalkylene group or polyoxyalkylene group R ^{5 in} this formula may be linear or branched, and may have two or more types of structures, but the carbon atom side of the two ends is always functional. It is assumed that it is bonded to the group B and the oxygen atom side is bonded to the carbonyl group. Further, if the carbon number of the oxyalkylene chain is too large, the reactivity of the vinyl compound as a raw material is lowered, so that the number is preferably up to 10. If the oxygen number of the polyoxyalkylene chain is too large, the water resistance and weather resistance of the resulting compound are reduced. Since it is inferior in properties, it is preferable to use up to 20. Specific examples include an oxyethylene group, an oxypropylene group,
Examples thereof include an oxyisobutylene group and a trioxyethylene group. Most preferred of these is the oxyethylene group.

The above formula (1) and a divalent group R ³ and ends in the structure unit (b) forming a A skeleton (2) thioether - divalent group R ⁴ in the ether group (b) is It may have a linear, branched or cyclic structure, and may contain a double bond or a hetero atom. Further, they may have two or more types of structures.

Among the above divalent groups R ³ and R ⁴ ,
(C) A group containing a group represented by —C ₂ H ₄ OCH ₂ OC ₂ H ₄ — is preferable.

The group A having such a structure may have a valence of 2 or more, but it is assumed that all the terminals contain a thioether group.

The terminal group of the functional group-terminated polysulfide compound of the present invention is the functional group B in the above general formulas (1) and (2), and is a hydroxyl group, a nitrile group, a carboxyl group, an ester group, an isocyanate group or an epoxy group. One or more groups consisting of a group and a halogen, and the most preferable group among these is a hydroxyl group. Further, the functional group-terminated polysulfide compound of the present invention may be trifunctional or higher.

The functional group-terminated polysulfide compound having the above structure is fluid at room temperature and has a molecular weight of 100 to 200,000, preferably 500 to 60,000.
0. [2] Method for producing functional group-terminated polysulfide compound As described above, in the functional group-terminated polysulfide compound of the present invention, (2) a vinyl compound having a functional group is added to a thiol group-terminated polysulfide compound. Is obtained by (1) thio - thio in Le-terminated polysulfide compound present invention - Le-terminated polysulfide compound in the main chain, _{(D) - (C 2 H 4 OCH} 2 OC 2 H 4
-S _X )-(however, x is an integer of 1 to 5) is contained, and (e) -C ₂ H ₄ is contained at the terminal.
Those having a thiol group represented by OCH ₂ OC ₂ H ₄ —SH are preferable. Such a polysulfide compound has fluidity at room temperature, and the number average molecular weight (Mn) is usually 100 to 200,000, preferably 400 to 5
It is 0000. Preferred examples of such polysulfide compounds are described in US Pat. No. 2,466,963.

[0026] In addition, in the main chain, _{^{(f) - (R 5 0) n}} -
(However, R ⁵ is an alkylene group having 2 to 4 carbon atoms, and n is 6 to
An integer of 200 is shown. ) And a polyether moiety represented by ( ₄ ) and (to)-(C ₂ H ₄ OCH ₂ OC ₂ H ₄ -S
_X) -, and _{- (CH 2 CH (OH)} CH 2 -S X) -
(Provided that x is an integer of 1 to 5) and has (CH) -C ₂ H ₄ OCH _{2 at the terminal.}
OC ₂ H ₄ -SH and / or -CH ₂ CH (OH) CH
A polysulfide polyether compound having a thiol group represented by _2- SH can also be used.

This polysulfide polyether compound is preferred because it has a lower viscosity at the same molecular weight than the above-mentioned polysulfide compound. Further, the polyether moiety of (f) and the structural unit of (g) may be bonded in any sequence, and the number average molecular weight (Mn) is usually 600 to 20.
0000, preferably 800 to 50,000. Preferred examples of such polysulfide polyether compounds are described, for example, in JP-A-4-363,325. (2) Vinyl compound having a functional group The vinyl compound having a functional group in the present invention has a general formula (4) and / or (5):

[0028]

Embedded image

[0029]

Embedded image (However, R ¹ is a hydrogen atom and / or a methyl group,
R ² is a divalent group. B is at least one functional group selected from the group consisting of hydroxyl group, nitrile group, carboxyl group, amino group, ester group, isocyanate group, epoxy group and halogen. ) Is represented.

The vinyl compound having a functional group in the present invention may have at least one of the structures of the above general formulas (4) and (5), that is, it contains a divalent group R ² in its skeleton. You don't have to. When R ² is contained, its structure may be linear or branched, and may contain a hetero atom. Further, it may have two or more types of structures.

Of these vinyl compounds, preferred are acrylic unsaturated monomers, and the above divalent group R ² is represented by the general formula (3):

[0032]

Embedded image (However, R ⁵ is an oxyalkylene group having 2 to 10 carbon atoms and / or a polyoxyalkylene group having 2 to 20 oxygen atoms, and the carbon atom at one end is bonded to the functional group B. It is represented by.). The oxyalkylene group or polyoxyalkylene group R ^{5 in} this formula may be linear or branched, and may have two or more types of structures, but the carbon atom side of the two ends is always functional. It is assumed that it is bonded to the group B and the oxygen atom side is bonded to the carbonyl group. Further, if the oxyalkylene chain has too many carbon atoms, the reactivity of the raw material acrylic unsaturated monomer decreases, so it is preferably up to 10, and if the polyoxyalkylene chain has too many oxygen atoms, the resulting compound Since the water resistance and weather resistance are poor, up to 20 are preferable. Specific examples thereof include an oxyethylene group, an oxypropylene group, an oxyisobutylene group and a trioxyethylene group. Most preferred of these is the oxyethylene group.

The functional group of the vinyl compound having a functional group of the present invention is the functional group B in the above general formulas (4) and (5), which is a hydroxyl group, a nitrile group, a carboxyl group, an ester group, an isocyanate group, One or more kinds of groups consisting of an epoxy group and a halogen, and the most preferable one among them is a hydroxyl group.

The most preferred example of the vinyl compound having a functional group as described above is 2-hydroxyethyl acrylate.
And 2-hydroxyethyl methacrylate. (3) Catalyst When a vinyl compound having a functional group as described above is reacted with a thiol group-terminated polysulfide compound, an appropriate amount of catalyst can be added in order to carry out the reaction quickly and reliably. . As the reaction catalyst, a basic catalyst is preferable, and a basic catalyst that dissolves in the raw material is more preferable. However, even when the reaction catalyst does not dissolve, it may be added after being dissolved in another solvent having a good compatibility with the raw material. Specific examples include triethylamine, triethylenediamine, 1,8
-Diazabicyclo (5,4,0) -7-undecene,
2,4,6-Tri (dimethylaminomethyl) pheno-
And potassium hydroxide, sodium hydroxide and the like. The addition amount of these catalysts is 0.001 to 1.0 with respect to 100 parts by weight of the thiol group-terminated polysulfide compound.
Parts by weight are preferred. (4) Reaction conditions The functional group-terminated polysulfide compound of the present invention is thio-
It is obtained by charging a vinyl group-terminated polysulfide compound with the entire amount of a vinyl compound having a functional group, mixing and reacting them. Alternatively, it can be obtained by reacting a thiol group-terminated polysulfide compound while dropping a vinyl compound having a functional group. In either case, an appropriate amount of catalyst may be added in advance before the reaction.

The amount of the vinyl compound having a functional group is 1 to 2.0 mol, preferably 1 to 1.5 mol, based on 1 mol of the thiol group in the thiol group-terminated polysulfide compound. If this amount is less than 1 mol, the thiol group in the raw material remains, and if it exceeds 2.0 mol, the vinyl compound remains, which is not preferable.

The reaction temperature is 0 ° C to 180 ° C, preferably 20 ° C to 150 ° C. Reaction temperature is 0
If it is less than ℃, the reaction time is too long and the reaction temperature is 180
If the temperature exceeds ℃, the thiol group-terminated polysulfide compound may be partially decomposed, which is not preferable. The reaction time is 1 to 48 hours, preferably 2 to 24 hours.

Further, when a basic catalyst is added during the reaction, it may be passed through an ion exchange resin to neutralize the base or an acid may be added after the addition reaction is completed.
As the acid to be added, a usual organic acid or inorganic acid may be used, and specific examples thereof include hydrochloric acid, citric acid, 2-ethylhexanoic acid, stearic acid and the like. The addition amount is preferably 1 to 2.0 equivalents with respect to the base of the basic catalyst.
It is not preferable because the acid remains in the obtained functional group-terminated polysulfide compound in excess of 2.0 equivalents.

[0038]

The present invention will be described in more detail by the following examples. Example 1 200 g of a polysulfide compound (manufactured by Toray Thiol Co., Ltd., trade name "Thiocol LP3", thiol group content 6.7% by weight) was charged into a reaction vessel, and polyethylene containing 2% by weight of potassium hydroxide was charged. 4 g of glycol solution was added, and nitrogen substitution was carried out sufficiently while stirring. Next, 58.1 g of 2-hydroxyethyl methacrylate was added and the reaction vessel was set to 50.
After immersion in an oil bath at ℃ for 1 hour and stirring, the bath temperature was raised to 70 ℃ and stirred for 2 hours to complete the reaction.

The obtained hydroxyl group-terminated polysulfide compound was a yellowish brown and uniformly transparent liquid polymer. The viscosity of this compound at 25 ° C. was 33 poise, and when titrated with iodine, the thiol group was completely disappeared. Moreover, when the obtained compound was analyzed using gel permeation chromatography (GPC) under the following conditions,
The peak of 2-hydroxyethyl methacrylate, which was 9% in area ratio before the reaction, was lowered to 1% or less. GPC analysis conditions column; G3000HxL + G2000HxL + G10
00HxL, manufactured by Toso Co., Ltd. Solvent; Tetrahydrofuran (THF) Column temperature; 30 ° C Flow rate; 1.0 ml / min Detector; Differential refractive index detector, RI MODEL504,
Example 2 manufactured by GL Science Co., Ltd. 200 g of a polysulfide compound (manufactured by Toray Thiol Co., Ltd., trade name "Thiocol LP3", thiol group content 6.7% by weight) was charged into a reaction vessel, 4 g of a polyethylene glycol solution containing 2% by weight of potassium hydroxide was added, and the atmosphere was sufficiently replaced with nitrogen while stirring. Next, 51.9 g of 2-hydroxyethyl acrylate was added, and the reaction vessel was heated to 50 ° C.
After immersing in the oil bath of 1 and stirring for 1 hour, the bath temperature was raised to 70 ° C. and stirring was continued for 6 hours to complete the reaction.

The obtained hydroxyl group-terminated polysulfide compound was a yellowish brown and uniformly transparent liquid polymer. The viscosity of this compound at 25 ° C. was 32 poise, and when titrated with iodine, the thiol group was completely disappeared. Further, when the obtained compound was analyzed by using gel permeation chromatography (GPC) under the above conditions,
The peak of 2-hydroxyethyl acrylate, which was 8% in area ratio before the reaction, was lowered to 1% or less. Example 3 A reaction vessel was charged with 200 g of a polysulfide compound (trade name “Thiocol LP3” manufactured by Toray Thiokol Co., Ltd., thiol group content 6.7 wt%), and 2.5 g of a polyethylene glycol solution containing 2 wt% potassium hydroxide was added. It was added, and nitrogen substitution was carried out sufficiently while stirring. Next, 23.3 g of acrylonitrile was added, the reaction vessel was immersed in an oil bath at 50 ° C. and stirred for 1 hour, then the bath temperature was raised to 70 ° C. and stirred for 2 hours to complete the reaction.

The resulting nitrile group-terminated polysulfide compound was a yellowish brown, uniformly transparent liquid polymer. The viscosity of this compound at 25 ° C. was 32 poise, and when titrated with iodine, the thiol group was completely disappeared.

[0042]

Industrial Applicability The functional group-terminated polysulfide compound of the present invention can be easily and highly purified by adding a vinyl compound having a functional group to the thiol group-terminated polysulfide compound, and the terminal thiol group can be obtained. There is no peculiar odor in the case of having, and a wide range of industrial applications becomes possible.

[Brief description of drawings]

1 is a GPC chart of the pre-reaction mixture of Example 1. FIG.

2 is a GPC chart of the post-reaction mixture of Example 1. FIG.

3 is a GPC chart of the pre-reaction mixture of Example 2. FIG.

4 is a GPC chart of the post-reaction mixture of Example 2. FIG.

Claims (6)

[Claims] 1. The following general formulas (1) and / or (2): Embedded image (However, R ¹ is a hydrogen atom and / or a methyl group,
R ² is a divalent group. B is at least one functional group selected from the group consisting of hydroxyl group, nitrile group, carboxyl group, amino group, ester group, isocyanate group, epoxy group and halogen. ), A in the general formulas (1) and (2) is (i)-(R ³ -S _X )-(wherein R ³ is a divalent group, and x is 1 to 5). A thioe represented by (b) to R ⁴ -S- (wherein R ⁴ is a divalent group) at the terminal.
A functional group-terminated polysulfide compound, which is a divalent or higher-valent group having a polysulfide structure containing a ter group. 2. The functional group-terminated polysulfide compound according to claim 1, wherein R ³ in the structural unit (a) and R ⁴ in the (b) terminal group are (c) -C ₂ H ₄ OC. _{n H 2n OC 2 H 4 -} (. Here, n is 1-2 is an integer) to contain a group represented by functionally terminated polysulfide compound characterized. 3. The functional group-terminated polysulfide compound according to claim 1 or 2, wherein the group R ² represented by the general formula (1) is represented by the general formula (3): (However, R ⁵ is an oxyalkylene group having 2 to 10 carbon atoms and / or a polyoxyalkylene group having 2 to 20 oxygen atoms, and the carbon atom at one end is bonded to the functional group B. A functional group-terminated polysulfide compound represented by the formula (1). 4. The functional group-terminated polysulfide compound according to claim 3, wherein the functional group B is a hydroxyl group. 5. The functional group-terminated polysulfide compound according to claim 4, wherein the group R ⁵ in the general formula is an oxyethylene group. 6. A method for producing a functional group-terminated polysulfide compound according to any one of claims 1 to 5, wherein the thiol group-terminated polysulfide compound is added to the following general formula (4) and / or (5): ] Embedded image (However, R ¹ is a hydrogen atom and / or a methyl group,
R ² is a divalent group. B is at least one functional group selected from the group consisting of hydroxyl group, nitrile group, carboxyl group, amino group, ester group, isocyanate group, epoxy group and halogen. ) A method for producing a functional group-terminated polysulfide compound, which comprises reacting a vinyl compound having a functional group represented by