JP2009001771A - Fluorine-containing polyether compound, method for producing the same and curable composition containing the same - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a fluorine-containing polyether compound which can be cured without the need of a Si-H bond-having fluorine-containing organo hydrogen siloxane compound, and gives a cured products being excellent in heat resistance, low temperature characteristics, chemical resistance, and molding processability and having improved mechanical strengths, to provide a method for producing the same, and to provide a curable composition containing the same. <P>SOLUTION: This method for producing a XC<SB>6</SB>H<SB>4</SB>NR<SP>1</SP>(CORfCOZ)<SB>n</SB>CORfCONR<SP>1</SP>C<SB>6</SB>H<SB>4</SB>X comprises reacting a fluorine-containing dicarboxylic acid fluoride: F(CORfCOZ)<SB>n</SB>CORfCOF äRf: CF(CF<SB>3</SB>)[OCF<SB>2</SB>CF(CF<SB>3</SB>)]<SB>l</SB>O(CF<SB>2</SB>)<SB>2</SB>O[CF(CF<SB>3</SB>)CF<SB>2</SB>O]<SB>m</SB>CF(CF<SB>3</SB>)} with an I or Br-substituted aromatic primary or secondary amine: XC<SB>6</SB>H<SB>4</SB>NHR<SP>1</SP>, wherein, Z is N(R<SP>2</SP>)R<SP>3</SP>N(R<SP>2</SP>) or a cyclic N(R<SP>4</SP>)<SB>2</SB>N. This fluorine-containing polyether compound is compounded with an aromatic borate, an organic palladium compound and a basic inorganic or organic compound (and an organic phosphorus compound), to prepare a curable composition. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

  The present invention relates to a fluorine-containing polyether compound, a method for producing the same, and a curable composition containing the same. More specifically, the present invention relates to a fluorine-containing polyether compound that is excellent in heat resistance and low-temperature properties and can give a cured product exhibiting good chemical resistance, a production method thereof, and a curable composition containing the same.

で表わされる化合物が知られている。
特開平１１−３４３３３６号公報 As the fluorine-containing polyether compound having a functional group at the molecular end, for example, a general formula

The compound represented by is known.
Japanese Patent Laid-Open No. 11-343336

で表わされる化合物が知られている。
特許２９９０６４６号公報 Further, as a more general compound obtained by oligomerizing the main chain structure of the above compound, a general formula

The compound represented by is known.
Japanese Patent No. 2990646

  The compounds represented by these general formulas are cured by a fluorine-containing organohydrogensiloxane compound having a plurality of Si-H groups in the molecule and a platinum compound catalyst, and have excellent properties (chemical resistance, heat resistance, low temperature It is said that an elastomeric molded product having characteristics) can be provided, and in particular, it can be used without loss of flexibility even under a low temperature condition of about -50 ° C. Moreover, the curable composition which has these as a main component has outstanding moldability, and also enables RIM molding. However, since this cured product has a siloxane bond in its intramolecular cross-linked structure, its mechanical strength decreases due to chemical degradation when used under conditions where acidic substances such as fluorine hydrogen are present. It may give undesirable results.

(X：ヨウ素原子または臭素原子) In addition, the present inventor has previously proposed a curable composition mainly comprising a fluorine-containing polyether compound represented by the following general formula (Japanese Patent Application No. 2007-99998).

(X: iodine atom or bromine atom)

  The fluorine-containing polyether compound can be cured using an appropriate curing agent and an organic palladium compound catalyst to obtain an elastomeric molded product. This curable composition exhibits appropriate fluidity at room temperature, and the cured product has good low-temperature characteristics and does not lose flexibility even at about -50 ° C. Further, since the crosslinked structure does not contain a siloxane bond, chemical deterioration does not occur even under acidic conditions. However, in the production of the above-mentioned fluorine-containing polyether compound, the hexafluoroisopropoxy repeating unit (l + m) is limited to about 130, and as a result, a molding machine obtained by curing the fluorine-containing polyether compound is obtained. Strength will be limited.

  The object of the present invention is that it can be cured without the need for a fluorine-containing organohydrogensiloxane compound having a Si-H bond, and is excellent in heat resistance, low temperature characteristics, chemical resistance and molding processability, and mechanical strength. Is to provide a fluorine-containing polyether compound that gives an improved cured product, a method for producing the same, and a curable composition containing the same.

(ここで、R¹は水素原子、炭素数1〜3のアルキル基またはフェニル基であり、Xはヨウ素原子または臭素原子であり、Xのフェニル基上の置換位置はNR¹結合置換基に対してm-またはp-位であり、Rfは一般式

で表わされる2価のパーフルオロポリエーテル基であり、ただしlおよびmはそれぞれ独立に10以上の整数であり、l+mは30〜130であり、Zは

であり、ただしR²は水素原子、炭素数1〜3のアルキル基またはフェニル基であり、R³は2価の炭素数2〜10の脂肪族炭化水素基、2価の炭素数6〜20の芳香族炭化水素基あるいは窒素原子、酸素原子または硫黄原子を含む炭素数2〜20の2価のヘテロ環化合物基であり、R⁴は2価の炭素数2〜5の脂肪族炭化水素基であり、nは1〜10の整数である)で表わされ、25℃における粘度が1〜1000Pa・sである含フッ素ポリエーテル化合物が提供される。 According to the invention, the general formula

(Where R ¹ is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a phenyl group, X is an iodine atom or a bromine atom, and the substitution position on the phenyl group of X is relative to the NR ¹ bond substituent. M- or p-position and Rf is the general formula

Wherein l and m are each independently an integer of 10 or more, l + m is 30 to 130, and Z is

R ² is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a phenyl group, R ³ is a divalent aliphatic hydrocarbon group having 2 to 10 carbon atoms, and a divalent carbon number 6 to 20 An aromatic hydrocarbon group or a divalent heterocyclic compound group having 2 to 20 carbon atoms containing a nitrogen atom, oxygen atom or sulfur atom, and R ⁴ is a divalent aliphatic hydrocarbon group having 2 to 5 carbon atoms And n is an integer of 1 to 10), and a fluorine-containing polyether compound having a viscosity of 1 to 1000 Pa · s at 25 ° C. is provided.

(ここで、Rfは一般式

で表わされる2価のパーフルオロポリエーテル基であり、ただしlおよびmはそれぞれ独立に10以上の整数であり、l+mは30〜130であり、Zは

であり、ただしR²は水素原子、炭素数1〜3のアルキル基またはフェニル基であり、R³は2価の炭素数2〜10の脂肪族炭化水素基、2価の炭素数6〜20の芳香族炭化水素基あるいは窒素原子、酸素原子または硫黄原子を含む炭素数2〜20の2価のヘテロ環化合物基であり、R⁴は2価の炭素数2〜5の脂肪族炭化水素基であり、nは1〜10の整数である)で表わされる含フッ素ジカルボン酸フルオリド化合物を、一般式

(ここで、R¹は水素原子、炭素数1〜3のアルキル基またはフェニル基であり、Xはヨウ素原子または臭素原子であり、Xのフェニル基上の置換位置はNR¹結合置換基に対してm-またはp-位である)で表わされる芳香族1級または2級アミン化合物と、好ましくはピリジン等の活性水素を有しない塩基性含窒素複素環化合物またはトリエチルアミン等の3級アミン化合物の存在下で反応させることにより製造される。 Such fluorine-containing polyether compounds have the general formula

(Where Rf is the general formula

Wherein l and m are each independently an integer of 10 or more, l + m is 30 to 130, and Z is

With the proviso R ² is a hydrogen atom, an alkyl group or a phenyl group having 1 to 3 carbon atoms, R ³ is a divalent aliphatic hydrocarbon group having 2 to 10 carbon atoms, divalent carbon atoms 6-20 An aromatic hydrocarbon group or a divalent heterocyclic compound group having 2 to 20 carbon atoms containing a nitrogen atom, oxygen atom or sulfur atom, and R ⁴ is a divalent aliphatic hydrocarbon group having 2 to 5 carbon atoms Wherein n is an integer of 1 to 10), the fluorine-containing dicarboxylic acid fluoride compound represented by the general formula

(Wherein R ¹ is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a phenyl group, X is an iodine atom or a bromine atom, and the substitution position on the phenyl group of X is relative to the NR ¹ bond substituent. An aromatic primary or secondary amine compound, preferably a basic nitrogen-containing heterocyclic compound having no active hydrogen such as pyridine, or a tertiary amine compound such as triethylamine. It is produced by reacting in the presence.

The fluorine-containing polyether compound thus obtained is used as a main component of the following curable composition. Specifically, the curable composition concerning this invention is comprised from the following each component.
Component (A) Fluorine-containing polyether compound 100 parts by weight
Component (B) Aromatic boronic ester compound 0.1-10 parts by weight
Component (C) 0 or divalent organopalladium compound 0.0001 to 1 part by weight
Component (D) Basic inorganic compound or basic organic compound 0.1 to 10 parts by weight
Component (E) Organic phosphorus compound 0-5 parts by weight

The fluorine-containing polyether compound according to the present invention can be produced from a readily available raw material by a simple reaction. Moreover, a curable fluorine-containing polyether composition can be formed with a specific hardening | curing agent and a hardening catalyst. This curable fluorine-containing polyether composition has good processability such as an appropriate fluidity at room temperature, and can be applied to various molding methods such as injection molding and RIM. Further, by curing it, a cured product having excellent heat resistance, low temperature characteristics and chemical resistance and further improved mechanical strength is obtained. Molded articles obtained by curing such compositions have various characteristics as described above, and therefore various types such as automobile fuel supply system seal materials, oil seal materials, aircraft fuel systems and hydraulic system seal materials, and semiconductor manufacturing equipment seal materials. It is suitably used for applications.

において、R¹は水素原子、炭素数1〜3のアルキル基またはフェニル基であり、特に製造面から水素原子またはメチル基であることが好ましい。ただし、水素原子の場合には、得られる含フッ素ポリエーテル化合物の粘度が高くなる傾向にある。Xは、ヨウ素原子または臭素原子であり、Xのフェニル基上の置換位置はNR¹結合置換基に対してm-またはp-位である。また、nは、1〜10の整数である。 Fluorinated polyether compound of the present invention

In the formula, R ¹ is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a phenyl group, and particularly preferably a hydrogen atom or a methyl group from the viewpoint of production. However, in the case of hydrogen atoms, the viscosity of the resulting fluorine-containing polyether compound tends to increase. X is an iodine atom or a bromine atom, and the substitution position on the phenyl group of X is the m- or p-position with respect to the NR ¹ -bonded substituent. N is an integer of 1 to 10.

で表わされる2価のパーフルオロポリエーテル基である。上記パーフルオロポリエーテル基において、lおよびmはそれぞれ独立に10以上の整数であり、l+mは30〜130である。 Rf is the general formula

A divalent perfluoropolyether group represented by the formula: In the perfluoropolyether group, l and m are each independently an integer of 10 or more, and l + m is 30 to 130.

であり、R²は水素原子、炭素数1〜3のアルキル基またはフェニル基であり、R³は2価の炭素数2〜10の脂肪族炭化水素基、炭素数6〜20の芳香族炭化水素基または窒素原子、酸素原子、硫黄原子等のヘテロ原子を含む2価の炭素数2〜20の複素環化合物基であり、R⁴は2価の炭素数2〜5の脂肪族炭化水素基である。 Z is

R ² is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a phenyl group, R ³ is a divalent aliphatic hydrocarbon group having 2 to 10 carbon atoms, and an aromatic carbon atom having 6 to 20 carbon atoms. hydrocarbon group or a nitrogen atom, an oxygen atom, a divalent heterocyclic compound group having 2 to 20 carbon atoms which contains a hetero atom such as a sulfur atom, R ⁴ is a divalent aliphatic hydrocarbon group having 2 to 5 carbon atoms It is.

等が挙げられる。また、本発明の含フッ素ポリエーテル化合物の25℃における粘度は、1〜1000Pa・sである。 As a specific example of Z,

Etc. Further, the viscosity of the fluorine-containing polyether compound of the present invention at 25 ° C. is 1 to 1000 Pa · s.

The fluorine-containing polyether compound of the present invention can be produced, for example, through the following series of steps.

The reaction in the first step can be performed by the method described in Patent Document 3. The oligomerization reaction with the diamine compound in the second step can be performed by the method described in Patent Document 4.
Japanese Patent Laid-Open No. 10-158387 USP 6,111,050

  In the final step, the reaction between the fluorine-containing dicarboxylic acid fluoride and the aromatic primary or secondary amine compound is carried out in the presence of a basic nitrogen-containing heterocyclic compound such as pyridine or a tertiary amine compound such as triethylamine. In a fluorine-containing solvent such as hydrofluorocarbon and hydrofluoroether, or a mixed solvent of these fluorine-containing solvent and aprotic non-fluorine solvent, the reaction is carried out at -50 to 150 ° C, preferably 0 to 100 ° C. Specific examples of the fluorine-containing solvent include HCFC-225, HFE-449 (Sumitomo 3M product HFE7100), HFE-569 (Sumitomo 3M product HFE-7200), and the like. Examples of the aprotic non-fluorinated solvent include diethyl ether, diisopropyl ether, cyclopentyl methyl ether, tetrahydrofuran, 1,4-dioxane and the like. In consideration of the solubility of the aromatic primary amine or secondary amine, it is more preferable to use a mixed solvent of a fluorinated solvent and an aprotic non-fluorinated solvent.

等が挙げられる。 The fluorine-containing polyether compound provided by the present invention can be a main component of the curable composition described below. As a specific example of the fluorine-containing polyether compound of the present invention,

Etc.

The curable fluorine-containing polyether composition of the present invention is composed of the following components containing the fluorine-containing polyether compound [component (A)] as a main component.
Component (A) Fluorine-containing polyether compound 100 parts by weight
Component (B) Aromatic boronic ester compound 0.1-10 parts by weight
Component (C) 0 or divalent organopalladium compound 0.0001 to 1 part by weight
Component (D) Basic inorganic compound or basic organic compound 0.1 to 10 parts by weight
Component (E) Organic phosphorus compound 0-5 parts by weight The curing reaction of the curable composition described above is based on a cross-coupling reaction of arylboronic acid or ester thereof with aryl halide (Suzuki-Miyaura reaction) with a palladium catalyst. Is.
Chem. Rev. 95 2457 (1995)

Hereinafter, embodiments of each component will be sequentially described.
In the fluorine-containing polyether compound represented by the above general formula as the component (A), R ¹ is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a phenyl group, but in an intramolecular or intermolecular hydrogen bond and curing. In order to avoid side reactions, an alkyl group having 1 to 3 carbon atoms or a phenyl group is preferred. In particular, a methyl group is selected from the viewpoint of easy availability of raw materials. X is either an iodine atom or a bromine atom, and an iodine atom is preferred because a faster curing rate can be obtained. Further, the substitution position on the phenyl group of X is the m- or p-position with respect to the NR ¹ bond substituent. When the substitution position of X is in the o-position, the hardness rate is lowered due to steric factors, which is not preferable. In the divalent perfluoropolyether group represented by Rf, l + m is 30 to 130, but in order to obtain a cured product having sufficient mechanical strength after curing, l + m is 50 to 130. It is preferable that

である。ここで、R²は水素原子、炭素数1〜3のアルキル基またはフェニル基であるが、分子内または分子間水素結合および硬化における副反応を避けるために、炭素数1〜3のアルキル基またはフェニル基が好ましい。特に原料の入手のし易さから、メチル基が選ばれる。R³は2価の炭素数2〜10の脂肪族炭化水素基、炭素数6〜20の芳香族炭化水素基、または窒素原子、酸素原子、硫黄原子等ヘテロ原子を含む2価の素炭数2〜20の複素環化合物基であり、R⁴は2価の炭素数2〜5の脂肪族炭化水素基である。Zの具体例としては、前記したものが挙げられる。 Z is

It is. Here, R ² is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a phenyl group, but in order to avoid side reactions in intramolecular or intermolecular hydrogen bonding and curing, an alkyl group having 1 to 3 carbon atoms or A phenyl group is preferred. In particular, a methyl group is selected because of easy availability of raw materials. R ³ is a divalent Motosumi number including a divalent aliphatic hydrocarbon group having 2 to 10 carbon atoms, an aromatic hydrocarbon group having 6 to 20 carbon atoms or a nitrogen atom, an oxygen atom, a sulfur atom or the like heteroatom A heterocyclic compound group having 2 to 20 carbon atoms, and R ⁴ is a divalent aliphatic hydrocarbon group having 2 to 5 carbon atoms. Specific examples of Z include those described above.

  The viscosity at 25 ° C. of the fluorine-containing polyether compound used as the component (A) is 1 to 1000 Pa · s, but considering the mechanical strength of the molded product obtained after curing, it is 10 to 1000 Pa · s. It is preferable.

を用いることができる。ここで、R⁵は炭素数2〜10の直鎖状または分岐状の2価の脂肪族炭化水素基であり、例えば-CH₂C(CH₃)₂CH₂-、-CH₂CH₂CH₂-、-C(CH₃)₂C(CH₃)₂-、-C(CH₃)₂CH₂C(CH₃)₂-等が挙げられる。具体的な例としては、1,3,5-トリス(4,4,5,5-テトラメチル-1,3,2-ジオキサボロラン-2-イル)ベンゼン、1,3,5-トリス(5,5-ジメチル-1,3,2-ジオキサボリナン-2-イル)ベンゼン、1,3,5-トリス(4,4,6,6-テトラメチル-1,3,2-ジオキサボリナン-2-イル)ベンゼンが挙げられる。好ましくは、1,3,5-トリス(4,4,5,5-テトラメチル-1,3,2-ジオキサボロラン-2-イル)ベンゼンが製造の容易さから選ばれる。
J. Appl. Poly. Sci. 76巻 1257頁 (2000) Component (B) is an aromatic boronic acid ester compound represented by the following general formula

Can be used. Here, R ⁵ is a linear or branched divalent aliphatic hydrocarbon group having 2 to 10 carbon atoms, for example, —CH ₂ C (CH ₃ ) ₂ CH ₂ —, —CH ₂ CH ₂ CH _2- , -C (CH ₃ ) ₂ C (CH ₃ ) _2- , -C (CH ₃ ) ₂ CH ₂ C (CH ₃ ) _2- and the like. Specific examples include 1,3,5-tris (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) benzene, 1,3,5-tris (5, 5-dimethyl-1,3,2-dioxaborinan-2-yl) benzene, 1,3,5-tris (4,4,6,6-tetramethyl-1,3,2-dioxaborinan-2-yl) benzene Is mentioned. Preferably, 1,3,5-tris (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) benzene is selected for ease of production.
J. Appl. Poly. Sci. 76 1257 (2000)

  The (B) component aromatic boronic acid ester compound is used in a proportion of 0.1 to 10 parts by weight, preferably 0.5 to 5 parts by weight, per 100 parts by weight of the (A) component fluorinated polyether compound. When the component (B) is less than this, the curing becomes insufficient or the mechanical strength of the obtained cured product is lowered. On the other hand, if it is used at a higher ratio, it is not economical because an effect commensurate with it cannot be expected.

  As the component (C) organic palladium compound used as the curing catalyst, a zero-valent or divalent organic palladium compound is used. The zero-valent palladium compound acts as a catalyst for the curing reaction in the zero-valent state as it is. The divalent organopalladium compound exhibits catalytic action after being reduced to zero valence by the component (A), the component (B), or the component (E), which will be described later. The component (C) organic palladium compound is used in a ratio of 0.0001 to 1 part by weight, preferably 0.001 to 0.2 part by weight, per 100 parts by weight of the component (A) fluorine-containing polyether compound. If the component (C) is less than this, sufficient curing will not be achieved, while it is not economical to use it in a proportion higher than this.

  As the zero-valent organic palladium compound, tetrakis (triphenylphosphine) palladium, bis (dibenzylideneacetone) palladium, tris (dibenzylideneacetone) dipalladium and the like are used. Examples of the divalent organic palladium compound include palladium acetate, allyl palladium chloride, bis (triphenylphosphine) palladium chloride, bis (tritert-butylphosphine) palladium chloride, and the like. In particular, palladium acetate is preferably used.

で表わされる(E)成分有機リン化合物を併用することが好ましい。 In the case of using an organic palladium compound that does not contain a phosphorus compound in the molecule such as palladium acetate, bis (dibenzylideneacetone) palladium, tris (dibenzylideneacetone) dipalladium, and allylpalladium chloride, as a stabilizer, the general formula

It is preferable to use an organic phosphorus compound (E) represented by

Here, R ⁶ , R ⁷ and R ⁸ are each independently a C1-C10 chain aliphatic hydrocarbon group, a C5-C12 cyclic aliphatic hydrocarbon group or carbon which may have a substituent. It is an aromatic hydrocarbon group of number 6-20. Specific examples of the organic phosphorus compound having an aliphatic hydrocarbon group include tricyclohexylphosphine, tri-tert-butylphosphine, triisopropylphosphine and the like.

で表わされるトリフェニルホスフィン化合物類または一般式

で表わされる、Buchwald配位子と総称される化合物群を用いることもできる。
ＵＳＰ ６，３０７，０８７ ＵＳＰ ６，２９４，６２７ In addition, as an organic phosphorus compound having an aromatic hydrocarbon group, a general formula

Triphenylphosphine compounds represented by the general formula

It is also possible to use a group of compounds generically referred to as Buchwald ligand.
USP 6,307,087 USP 6,294,627

Here, A, B and C are each independently a hydrogen atom, an alkoxy group having 1 to 5 carbon atoms or an alkoxy group having 1 to 3 carbon atoms or a dialkylamino group. R ¹⁰ is a linear or cyclic aliphatic hydrocarbon group having 1 to 6 carbon atoms. Examples of triphenylphosphine compounds include triphenylphosphine, tris (4-methoxyphenyl) phosphine, tris (1,3,5-triisopropylphenyl) phosphine, and the like. Specific examples of the Buchwald ligand include (2-biphenyl) dicyclohexylphosphine, 2-dicyclohexylphosphino-2 ', 6'-dimethoxybiphenyl, 2-di-tert-butylphosphino-2', 4 ', 6 Examples thereof include compounds such as '-triisopropylbiphenyl and 2-dicyclohexylphosphino-2'-(N, N-dimethylamino) biphenyl.

で表わされる二座配位子有機リン化合物も用いることができる。ここで、R⁹は置換基を有し得るフェニル基または炭素数1〜6の脂肪族炭化水素基であり、Yは2価の炭素数1〜10の脂肪族炭化水素基、炭素数6〜20の芳香族炭化水素基またはメタロセン基である。 Other general formulas with two phosphorus atoms in the molecule

A bidentate organophosphorus compound represented by the formula can also be used. Here, R ⁹ is a phenyl group which may have a substituent or an aliphatic hydrocarbon group having 1 to 6 carbon atoms, Y is a divalent aliphatic hydrocarbon group having 1 to 10 carbon atoms, 6 to 6 carbon atoms 20 aromatic hydrocarbon groups or metallocene groups.

  Specific examples include 1,2-bis (diphenylphosphino) ethane, 1,3-bis (diphenylphosphino) propane, 1,4-bis (diphenylphosphino) butane, 1,1'-bis (diphenylphosphine). Examples include compounds such as fino) ferrocene, 1,1′-bis (ditert-butylphosphino) ferrocene, and 2,2′-bis (diphenylphosphino) -1,1′-binaphthalene.

  The (E) component organic phosphorus compound is used in an amount of 0.5 to 10 molar equivalents, preferably 1 to 4 molar equivalents, relative to the Pd atom of the (C) component organic palladium compound. The component (A) is preferably used at a ratio of 0.1 to 2 parts by weight per 100 parts by weight.

  The basic inorganic compound or basic organic compound of component (D) includes lithium carbonate, sodium carbonate, potassium carbonate, cesium carbonate, lithium hydrogen carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate and other alkali metal carbonates or hydrogen carbonates. Alkali metal phosphates or hydrogen phosphates such as lithium phosphate, sodium phosphate and potassium phosphate, oxides or hydroxides of alkali metals or alkaline earth metals such as magnesium oxide, calcium hydroxide and sodium hydroxide Products, alkali metal fluorides such as potassium fluoride, sodium fluoride and cesium fluoride, alkali metal acetates such as potassium acetate, sodium methoxide and organic amines. A preferred example is potassium phosphate. The (D) component basic inorganic compound or basic organic compound is used in a proportion of 0.1 to 10 parts by weight, preferably 1 to 10 parts by weight, per 100 parts by weight of the (A) component fluorine-containing polyether compound. If component (D) is not added, the curing reaction may be very slow or may not occur at all.

  In the curable fluorine-containing polyether composition, in addition to these components, various fillers, reinforcing agents, pigments and the like having an amount and a purity that do not inhibit the curing reaction are used as appropriate. The composition is prepared by kneading using a three-roll mill, a planetary mixer, etc., and the mixture is cured at room temperature to 200 ° C. by compression molding, injection molding, RIM molding, etc. for about 1 to 60 minutes. If necessary, oven vulcanization (secondary vulcanization) is performed at 50 to 250 ° C. for about 1 to 30 hours.

  Next, the present invention will be described with reference to examples.

攪拌装置、温度センサ、ガス導入口およびドライアイス／エタノール冷却凝縮器を備えた内容量1Lのガラス製反応容器を低温恒温槽に設置し、ジアルコキシド化合物 CsOCF₂CF(CF₃)OCF₂CF₂OCF(CF₃)CF₂OCs を23ミリモルを含むテトラグライム溶液44gを仕込んだ。内温を-33〜-30℃に調整した後、ガス導入口よりヘキサフルオロプロペンを27g仕込んだ。次に、ヘキサフルオロプロペンオキシドを10g/hr、ヘキサフルオロプロペンを4g/hrの供給速度で反応容器内に仕込んだ。27時間経過後、ガスの供給を停止し、さらに1時間-33〜-30℃に内温を保った。減圧下でヘキサフルオロプロペンを反応系内より除去した後、室温までゆっくり昇温した。さらに100℃まで昇温し、減圧下でヘキサフルオロプロペンオリゴマーを反応混合物より除去した。このようにして、フッ化セシウム、テトラグライムおよび含フッ素ジカルボン酸フルオリドからなる混合物を淡黄色粘稠な懸濁液として298g得た。これを精製せずに、次の工程に用いた。 Reference example 1
Preparation of fluorinated dicarboxylic acid fluoride compounds

A 1 L glass reaction vessel equipped with a stirrer, temperature sensor, gas inlet, and dry ice / ethanol cooled condenser is placed in a low-temperature thermostatic chamber, and dialkoxide compound CsOCF ₂ CF (CF ₃ ) OCF ₂ CF ₂ 44 g of a tetraglyme solution containing 23 mmol of OCF (CF ₃ ) CF ₂ OCs was charged. After adjusting the internal temperature to -33 to -30 ° C, 27 g of hexafluoropropene was charged from the gas inlet. Next, hexafluoropropene oxide was charged into the reaction vessel at a feed rate of 10 g / hr and hexafluoropropene at 4 g / hr. After 27 hours, the gas supply was stopped, and the internal temperature was kept at -33 to -30 ° C for another hour. After removing hexafluoropropene from the reaction system under reduced pressure, the temperature was slowly raised to room temperature. The temperature was further raised to 100 ° C., and the hexafluoropropene oligomer was removed from the reaction mixture under reduced pressure. In this manner, 298 g of a mixture consisting of cesium fluoride, tetraglyme and fluorine-containing dicarboxylic acid fluoride was obtained as a pale yellow viscous suspension. This was used in the next step without purification.

s＝F^a(-131ppm)ピーク積分値
t＝F^b(-133ppm)ピーク積分値
u＝F^c(-146ppm)ピーク積分値
注) ケミカルシフトはCFCl₃基準
二官能性比＝(t／s-0.5)／(t／s+0.5)＝0.90
ヘキサフルオロプロペンオキシド数平均重合度＝4u／(2t+s)＝70 A part of the mixture was converted into an ester form with methanol, and then the number average degree of polymerization of hexafluoropropene oxide and the bifunctional ratio (molar fraction with hexafluoropropene oxide oligomer) were determined by ¹⁹ F-NMR.

s = F ^a (-131ppm) Peak integrated value
t = F ^b (-133ppm) Peak integral value
u = F ^c (-146ppm) peak integral value
Note) Chemical shift is based on CFCl ₃ Bifunctional ratio = (t / s-0.5) / (t / s + 0.5) = 0.90
Hexafluoropropene oxide number average degree of polymerization = 4u / (2t + s) = 70

を、僅かに黄色味を帯びた透明な液体として35g得た。E型粘度計(東機産業製TEV-22)により粘度を測定したところ、15Pa・s(25℃)であった。
¹⁹F-NMR(ケミカルシフトはCFCl₃基準)： -123ppm(F^b)
-146ppm(F^c)
¹H-NMR(ケミカルシフトはTMS基準)： 7.5ppm(H^a)
6.7ppm(H^b)
3.0ppm(H^c)
IR(neat)： 1702cm^-1(C=O)
1488cm^-1(Ar) Reference example 2
43 g (about 3.6 mmol) of a mixture comprising the fluorine-containing dicarboxylic acid fluoride, cesium fluoride and tetraglyme obtained in Reference Example 1 was dissolved in 50 ml of a fluorine-containing solvent (Sumitomo 3M product HFE-7100), and triethylamine was dissolved therein. 1.4 g (14 mmol) and 20 ml of diethyl ether were added. To this, 2.5 g (11 mmol) of p-iodo-N-methylaniline was added and reacted at room temperature for 1 hour. The obtained reaction mixture was added to saturated brine, and the separated organic layer was dried over anhydrous magnesium sulfate and filtered. After distilling off the fluorine-containing solvent and diethyl ether from the filtrate under reduced pressure, the resulting viscous liquid was washed several times with diethyl ether, and then diethyl ether was completely distilled off under reduced pressure. In this way, fluorine-containing polyether compound [PFPE-I]

35 g were obtained as a slightly yellowish transparent liquid. When the viscosity was measured with an E-type viscometer (TEV-22 manufactured by Toki Sangyo), it was 15 Pa · s (25 ° C.).
¹⁹ F-NMR (chemical shift based on CFCl ₃ ): -123 ppm (F ^b )
-146ppm (F ^c )
¹ H-NMR (chemical shift is based on TMS): 7.5 ppm (H ^a )
6.7ppm (H ^b )
3.0ppm (H ^c)
IR (neat): 1702cm ^-1 (C = O)
1488cm ^-1 (Ar)

を黄色味を帯びた液体として35g得た。E型粘度計(東機産業製TEV-22)により粘度を測定したところ、90Pa・s(25℃)であった。
IR(neat)： 1700cm^-1(C=O)
1490cm^-1(Ar) Example 1
50 g (about 4.1 mmol) of a mixture comprising fluorine-containing dicarboxylic acid fluoride, cesium fluoride and tetraglyme obtained in Reference Example 1 was dissolved in 50 ml of a fluorine-containing solvent (HFE-7100), and 1.6 g of triethylamine ( 16 mmol) and 20 ml of diethyl ether were added. To this, 20 ml of diethyl ether solution of 0.8 g (2.9 mmol) of N, N′-dimethyl-p-phenylenediamine was added at room temperature over 30 minutes, and the reaction was further performed for 30 minutes. Subsequently, 0.5 g (2.0 mmol) of p-iodo-N-methylaniline was added, and the reaction was further performed for 1 hour. The obtained reaction mixture was added to saturated brine, and the separated organic layer was dried over anhydrous magnesium sulfate and filtered. After distilling off the fluorine-containing solvent and diethyl ether from the filtrate under reduced pressure, the resulting viscous liquid was washed several times with diethyl ether, and then diethyl ether was completely distilled off under reduced pressure. Thus, a fluorine-containing polyether compound

Was obtained as a yellowish liquid. When the viscosity was measured with an E-type viscometer (TEV-22 manufactured by Toki Sangyo), it was 90 Pa · s (25 ° C.).
IR (neat): 1700cm ^-1 (C = O)
1490cm ^-1 (Ar)

Example 2
100 parts by weight of the fluorine-containing polyether compound of Example 1
1,3,5-tris (4,4,5,5-tetramethyl-1,3,2-1.5 parts by weight
Dioxaborolan-2-yl) benzene palladium acetate 0.07 parts by weight
(2-Biphenyl) dicyclohexylphosphine 0.23 parts by weight Potassium phosphate 2.3 parts by weight or more of each component was added to a mixed solvent consisting of 120 parts by weight of ethanol, 25 parts by weight of water and 300 parts by weight of benzotrifluoride, and room temperature in a nitrogen atmosphere. The volatiles were removed at 40 ° C. under reduced pressure. The obtained mixture was mixed with 10 parts by weight of acetylene carbon black to prepare a curable composition.

  This curable composition was compression-molded at 130 ° C. for 10 minutes, and then subjected to oven vulcanization (secondary vulcanization) at 80 ° C., 5 hours, and 200 ° C. for 10 hours in a nitrogen atmosphere in order to obtain a test piece. It was.

About the obtained curable composition and vulcanizate, the following each item was measured.
Curing test: using a Monsanto disk rheometer, 130 ° C. at t _10, t _90, ML, measured normal state physical properties values of MH: JIS K6250, K6253 compliant compression set: ASTM D395 Method B compliant
For P-24 O-ring, 200 ° C., the low temperature measurement value of 70 hours characteristics: in compliance with ASTM D1329, the measurement methanol immersion test values of TR _10, TR _70: after immersion for 70 hours in a 25 ° C. methanol Measure volume change rate

Example 3
In Example 2, a curable composition using 0.18 parts by weight of triphenylphosphine was used instead of (2-biphenyl) dicyclohexylphosphine.

Comparative Example In Example 2,
100 parts by weight of the fluorine-containing polyether compound of Reference Example 2
1,3,5-tris (4,4,5,5-tetramethyl-1,3,2-3 parts by weight
Dioxaborolan-2-yl) benzene palladium acetate 0.15 parts by weight
(2-Biphenyl) dicyclohexylphosphine 0.5 parts by weight Potassium phosphate A curable composition comprising 5 parts by weight or more of each component was used.

The measurement results of Examples 2 to 3 and the comparative example are shown in the following table.
table
Measurement item Example 2 Example 3 Comparative example
[Curing test]
Test temperature (℃) 130 130 130
t ₁₀ (min) 0.4 0.5 0.4
t ₉₀ (min) 0.8 0.9 1.0
ML (dN ・ m) 0.3 0.3 0.2
MH (dN ・ m) 4.7 4.8 2.5
[Normal properties]
Hardness 53 53 52
100% modulus (MPa) 2.1 2.0 1.2
Strength at break (MPa) 4.2 4.0 2.6
Elongation at break (%) 240 240 260
(Compression set)
200 ℃, 70 hours (%) 45 48 60
(Low temperature characteristics)
TR ₁₀ (℃) -48 -48 -48
TR ₇₀ (℃) -37 -37 -34
[Methanol immersion test]
Volume change rate (%) +3 +3 +3

Claims (12)

General formula

(Wherein R ¹ is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a phenyl group, X is an iodine atom or a bromine atom, and the substitution position on the phenyl group of X is relative to the NR ¹ bond substituent. M- or p-position, and Rf is a divalent perfluoropolyether group represented by the following general formula:

However, l and m are each independently an integer of 10 or more, l + m is 30 to 130, and Z is

R ² is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a phenyl group, R ³ is a divalent aliphatic hydrocarbon group having 2 to 10 carbon atoms, and a divalent carbon number 6 to 20 An aromatic hydrocarbon group or a divalent heterocyclic compound group having 2 to 20 carbon atoms containing a nitrogen atom, oxygen atom or sulfur atom, and R ⁴ is a divalent aliphatic hydrocarbon group having 2 to 5 carbon atoms And n is an integer of 1 to 10, and the viscosity at 25 ° C. is 1 to 1000 Pa · s.   2. The fluorine-containing polyether compound according to claim 1, wherein X in the general formula is an iodine atom. The fluorine-containing polyether compound according to claim ¹ , wherein R ¹ in the general formula is a methyl group. General formula

(Where Rf is the general formula

Wherein l and m are each independently an integer of 10 or more, l + m is 30 to 130, and Z is

R ² is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a phenyl group, R ³ is a divalent aliphatic hydrocarbon group having 2 to 10 carbon atoms, and a divalent carbon number 6 to 20 divalent or a heterocyclic compound group, R ⁴ is a divalent aliphatic hydrocarbon group having 2 to 5 carbon atoms of an aromatic hydrocarbon group or a nitrogen atom, having 2 to 20 carbon atoms containing an oxygen atom or a sulfur atom Wherein n is an integer of 1 to 10), the fluorine-containing dicarboxylic acid fluoride compound represented by the general formula

(Wherein R ¹ is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a phenyl group, X is an iodine atom or a bromine atom, and the substitution position on the phenyl group of X is relative to the NR ¹ bond substituent. 2. The method for producing a fluorinated polyether compound according to claim 1, wherein the reaction is carried out with an aromatic primary or secondary amine compound represented by the formula (M- or p-position).   The method for producing a fluorinated polyether compound according to claim 4, wherein the reaction is carried out in the presence of a basic nitrogen-containing heterocyclic compound or a tertiary amine compound having no active hydrogen. (A) 100 parts by weight of the fluorine-containing polyether compound according to claim 1
(B) General formula

(Where R ⁵ is a straight chain of 2 to 10 carbon atoms or
(This is a branched divalent aliphatic hydrocarbon group.)
Aromatic boronic acid ester compound represented by 0.1 to 10 parts by weight
(C) Zero or divalent organopalladium compound 0.0001 to 1 part by weight
(D) Basic inorganic compound or basic organic compound 0.1 to 10 parts by weight
(E) General formula

(Here, R ⁶ , R ⁷ and R ⁸ are each independently a chain aliphatic hydrocarbon group having 1 to 10 carbon atoms and a cyclic aliphatic hydrocarbon having 5 to 12 carbon atoms which may have a substituent. (A hydrocarbon group or an aromatic hydrocarbon group having 6 to 20 carbon atoms)
Or general formula

(Where R ⁹ is a phenyl group which may have a substituent or an aliphatic hydrocarbon group having 1 to 6 carbon atoms;
Y is a divalent aliphatic hydrocarbon group having 1 to 10 carbon atoms,
(It is an aromatic hydrocarbon group or metallocene group having 6 to 20 carbon atoms)
A curable fluorine-containing polyether composition comprising 0 to 5 parts by weight of an organic phosphorus compound represented by the formula:   The curable fluorine-containing polyether composition according to claim 6, wherein a fluorine-containing polyether compound in which X is an iodine atom is used as the component (A). (B) Component aromatic boronic acid ester compound is 1,3,5-tris (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) benzene

The curable fluorine-containing polyether composition according to claim 6.   The curable fluorinated polyether composition according to claim 6, wherein the divalent organic palladium compound (C) is palladium acetate.   The curable fluorine-containing polyether composition according to claim 6, wherein the component (D) basic inorganic compound is potassium phosphate. Component (E) is an organic phosphorus compound represented by the following general formula:

(Here, A, B, and C are each independently a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or an alkoxy group or dialkylamino group having an alkyl group having 1 to 3 carbon atoms.)
The curable fluorine-containing polyether composition of Claim 6 represented by these. Component (E) is an organic phosphorus compound represented by the following general formula:

(Here, A, B, and C are each independently a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or an alkoxy group or dialkylamino group having an alkyl group having 1 to 3 carbon atoms, (R ¹⁰ is a linear or cyclic aliphatic hydrocarbon group having 1 to 6 carbon atoms)
The curable fluorine-containing polyether composition of Claim 6 represented by these.