JP4664686B2 - Process for producing polysilanes - Google Patents

Description

  The present invention relates to a method for efficiently producing polysilane by electrode reaction in a distribution system (particularly a distribution system using a microreactor).

  Polysilanes are attracting attention as ceramic precursors, optoelectronic materials (for example, photoelectrophotographic materials such as photoresists and organic photoreceptors, optical transmission materials such as optical waveguides, optical recording materials such as optical memories, and materials for electroluminescent elements). ing.

  As a method for producing polysilane, dialkyldihalosilane or dihalotetraalkyldisilane is reductively reduced in toluene solvent at a temperature of 100 ° C. or higher and with strong stirring using an alkali metal such as sodium metal as a reducing agent. Coupling methods are known [J. Am. Chem. Soc. 103 (1981), p. 7352 (Non-Patent Document 1)]. However, in the above method, it is necessary to heat and strongly stir and disperse the alkali metal that ignites in the air, so that there is a big problem in safety in production on an industrial scale. There are also problems with quality, such as the molecular weight distribution being multimodal.

In order to solve these problems, a method for producing polysilane using an electrode reaction has been proposed. For example, in Japanese Patent No. 3291564 (Patent Document 1), a perchlorate as a supporting electrolyte and an aprotic solvent are used, and Mg, Cu or Al is used as one electrode, and the one electrode is used as the other electrode. Using the same or different kinds of conductive materials, two types of halosilanes among dihalosilane, trihalosilane and tetrahalosilane are subjected to electrode reaction, and the network polysilane is produced by switching the polarity of the electrodes at intervals of 1 to 20 seconds. A method is disclosed. Further, in Japanese Patent No. 3106205 (Patent Document 2), a tetraalkylammonium perchlorate as a supporting electrolyte and an aprotic solvent are used, and an electrode reaction using Mg as an anode is subjected to dihalosilane to produce polysilane. A method is disclosed. However, in the electrode reaction, a large amount of Joule heat is generated with energization, and it is necessary to remove Joule heat. However, in the batch method, it is difficult to control the reaction temperature, and it is difficult to control the molecular weight of polysilane.
Japanese Patent No. 3291564 (Claims 1 to 4) Japanese Patent No. 3106205 (Claim 1) J. et al. Am. Chem. Soc. 103 (1981), p. 7352

  Accordingly, an object of the present invention is to provide a method capable of efficiently producing polysilane even in a distribution system regardless of the type of electrode material.

  Another object of the present invention is to provide a method for producing a polysilane in which the reaction temperature can be easily controlled and the molecular weight can be easily adjusted.

  As a result of intensive investigations to achieve the above-mentioned problems, the inventors of the present invention can efficiently react even in a flow system, regardless of the type of electrode material, when Mg ions are included in the mixture used for the electrode reaction, and The present inventors have found that the reaction temperature can be easily controlled by reacting in a flow system, and the molecular weight of polysilane can be easily controlled.

  That is, the method for producing a polysilane of the present invention is a method for producing a polysilane by subjecting a halosilane compound to an electrode reaction, the halosilane compound, magnesium ions, a perchlorate as a supporting electrolyte, and an aprotic solvent. Is continuously supplied to a flow-through microreactor, and direct current is passed through the mixture.

  The halosilane compound is represented by a monohalosilane compound represented by the following formula (1), a dihalosilane compound represented by the following formula (2), a trihalosilane compound represented by the following formula (3), and the following formula (4). Or at least one selected from tetrahalosilane compounds.

(Wherein X ^{1 to} X ⁴ are the same or different and each represents a halogen atom, and R ^{1 to} R ³ are the same or different and each represents a hydrogen atom, an organic group or a silyl group)
The halosilane compound may be a mono to trihalosilane compound (for example, dialkylmonoarylmonohalosilane, monoalkylmonoaryldihalosilane, monoaryltrihalosilane, etc.).

As the supporting electrolyte, alkali metal perchlorate can be used, and magnesium halide can be used as a magnesium ion source. The aprotic solvent may be an aprotic polar solvent such as ether such as tetrahydrofuran and 1,2-dimethoxyethane. In the electrode reaction, a material that is non-eluting by energization may be used as at least the anode material. For example, the positive electrode may be a carbon electrode (such as a fine carbon electrode). Further, the mixture may be passed through the reactor at a space velocity of about ¹ to 10 h ⁻¹ .

  In this specification, the term “polysilane” is used to include oligosilanes such as disilane.

  In the present invention, Mg ions are contained in the substrate mixture to be subjected to the electrode reaction, so that polysilane can be efficiently produced regardless of the type of the electrode material even in the flow system. In addition, since the electrode reaction can be carried out in a flow system, the reaction temperature can be easily controlled. As a result, the molecular weight can be easily controlled, and high-quality polysilane can be produced. Furthermore, when a non-eluting or non-consumable material (for example, a carbon material) is used as the anode material, the polysilane can be stably and continuously produced without replacing the electrode.

  In the present invention, a mixture (substrate mixture or raw material mixture) containing a halosilane compound, magnesium ions, a perchlorate as a supporting electrolyte, and an aprotic solvent is continuously supplied to a flow-through microreactor, and the mixture A polysilane is produced by passing a direct current through the substrate.

(Halosilane compound)
As the halosilane compound used for the electrode reaction, a mono- to tetrahalosilane compound can be used. Examples of the mono to tetrahalosilane compound include compounds represented by the above formulas (1) to (4).

In the above formulas (1), (2) and (3), the organic group represented by R ^{1 to} R ³ is an alkyl group [straight chain such as methyl, ethyl, propyl, isopropyl, butyl and t-butyl groups. Or a branched C _1-10 alkyl group (preferably a C _1-6 alkyl group, particularly a C _1-4 alkyl group, etc.), a cycloalkyl group (C _5-8 cycloalkyl group such as a cyclohexyl group, in particular C _5-6 cycloalkyl group and the like), aryl groups (C _6-10 aryl groups such as phenyl and naphthyl groups), aralkyl groups [C _6-10 aryl-C _1-6 alkyl groups such as benzyl and phenethyl groups ( C _6-10 aryl-C _1-4 alkyl group etc.), etc.], as well as alkoxy groups [C _1-10 alkoxy groups such as methoxy, ethoxy, propoxy, isopropoxy, butoxy and t-butoxy groups] (Preferably C _1-6 Arco Xy group, especially C _1-4 alkoxy group, etc.], amino group, and N-substituted amino group (N-mono or di-substituted by the above alkyl group, cycloalkyl group, aryl group, aralkyl group, acyl group, etc.) Substituted amino group, etc.).

The aryl group constituting the alkyl group, cycloalkyl group, aryl group, or aralkyl group may have a substituent. Examples of such a substituent include the above-exemplified alkyl groups (especially C _1-6 alkyl group and the like) and the above-exemplified alkoxy groups. The number of substituents is not particularly limited, and may be one or plural (for example, 2 to 4). Examples of the organic group having such a substituent include C _1-6 alkyl C _6-10 aryl groups such as tolyl, xylenyl, ethylphenyl, and methylnaphthyl groups (preferably mono to tri C _1-4 alkyl C _{6 -10} aryl groups, especially mono or di C _1-4 alkylphenyl groups); C _1-10 alkoxy C _6-10 aryl groups such as methoxyphenyl, ethoxyphenyl, _{methoxynaphthyl} groups (preferably C _1-6 alkoxy C) _6-10 aryl group, especially C _1-4 alkoxyphenyl group, etc.).

The silyl group represented by R ^{1 to} R ³ may be a substituted silyl group substituted with the above-exemplified alkyl group, cycloalkyl group, aryl group, aralkyl group, and / or alkoxy group.

  Of these groups, hydrogen atoms or hydrocarbon groups, particularly hydrocarbon groups (alkyl groups, aryl groups, aralkyl groups, etc.) are preferred.

In the formulas (1) to (4), the halogen atoms represented by X ^{1 to} X ⁴ include F, Cl, Br, and I atoms. Of these halogen atoms, Cl and Br (especially Cl) atoms are particularly preferred.

(1) Monohalosilane Compound In the monohalosilane compound of the formula (1), the groups R ^{1 to} R ³ are preferably hydrocarbon groups such as alkyl groups and aryl groups.

Specific examples of the monohalosilane compound include, for example, trialkylmonohalosilanes (such as tri-C _1-6 alkyl monohalosilanes such as trimethylchlorosilane) and dialkyl monoaryl monohalosilanes (di-C _1-6 alkyl such as dimethylphenylchlorosilane). mono- such C _6-10 aryl monohaloalkyl silane), etc. mono C _1-6 alkyl di C _6-10 aryl monohaloalkyl silane such as monoalkyl diaryl monohaloalkyl silane (methyl diphenyl chlorosilane), triaryl monohaloalkyl silane (triphenyl chlorosilane And tri-C _{6-10 arylhalosilane} ). A monohalosilane compound can be used individually or in combination of 2 or more types.

(2) Dihalosilane Compound In the dihalosilane compound of the above formula (2), the groups R ¹ and R ² are preferably hydrocarbon groups such as alkyl groups and aryl groups.

Specific examples of dihalosilane compounds include, for example, dialkyldihalosilanes (such as diC _1-4 alkyldihalosilanes such as dimethyldichlorosilane), monoalkylmonoaryldihalosilanes (monoC _1- such as methylphenyldichlorosilane). ₄ alkylmono C _6-10 aryl dihalosilane), diaryl dihalosilane (di C _6-10 aryl dihalosilane such as diphenyldichlorosilane) and the like. A dihalosilane compound can be used individually or in combination of 2 or more types.

(3) Trihalosilane compound In the trihalosilane compound represented by the formula (3), R ¹ is usually an alkyl group, a cycloalkyl group, an optionally substituted aryl group, an aralkyl group or other carbonized group. A hydrogen group is preferred.

Specific examples of the trihalosilane compound include monoalkyltrihalosilanes (mono-C _1-6 alkyltrihalosilanes such as methyltrichlorosilane, butyltrichlorosilane, t-butyltrichlorosilane, and hexyltrichlorosilane), monocycloalkyltrihalosilanes ( Examples thereof include mono C _6-10 cycloalkyl trihalo silanes such as cyclohexyl trihalosilane) and monoaryl trihalo silanes (mono C _6-10 aryl trihalo silanes such as phenyl trichlorosilane, tolyl dichlorosilane, and xylyl trichlorosilane). A trihalosilane compound can be used individually or in combination of 2 or more types.

(4) Tetrahalosilane compound Specific examples of the tetrahalosilane compound include tetrachlorosilane, dibromodichlorosilane, and tetrabromosilane.

  These halosilane compounds can be used alone or in combination of two or more. Among the halosilane compounds, mono to trihalosilane compounds (for example, dialkylmonoarylmonohalosilane, monoalkylmonoaryldihalosilane, monoaryltrihalosilane, etc.) are particularly preferable. In addition, when using in combination of 2 or more types of halosilane compounds, the mixing ratio of each compound is not specifically limited.

  In addition, it is preferable that a halosilane compound is highly pure, for example, you may distill and use before use.

(Supporting electrolyte)
The supporting electrolyte is usually a perchlorate, for example, an alkali metal perchlorate such as sodium perchlorate or lithium perchlorate; perchlorine such as tetra-n-butylammonium perchlorate or tetraethylammonium perchlorate. Examples include tetraalkylammonium acid. These perchlorates may be used alone or in combination of two or more. Of the perchlorates, alkali metal perchlorate (particularly lithium perchlorate) and tetra-n-butylammonium perchlorate are preferred. In addition, you may use a conventional supporting electrolyte together in the range which does not inhibit an electrode reaction.

(Magnesium ion source)
In the electrode reaction, magnesium ions function as a reaction catalyst. The magnesium ion source is not particularly limited as long as it is a compound that can be dissolved in an aprotic solvent (particularly an aprotic polar solvent) to generate magnesium ions. For example, magnesium halides such as magnesium chloride and magnesium bromide And magnesium salts (for example, oxyacid salts such as magnesium sulfate and magnesium phosphate). These magnesium ion sources can be used alone or in combination of two or more.

(Aprotic solvent)
As the reaction solvent, aprotic solvents can be widely used. For example, ethers (1,4-dioxane, tetrahydrofuran, tetrahydropyran, diethyl ether, diisopropyl ether, 1,2-dimethoxyethane, bis (2-methoxyethyl) Cyclic or linear C _4-6 ether such as ether), carbonates (such as propylene carbonate), nitriles (such as acetonitrile and benzonitrile), amides (such as dimethylformamide and dimethylacetamide), sulfoxides (such as dimethyl sulfoxide) , Halogen-containing compounds (halogenated hydrocarbons such as methylene chloride, chloroform, bromoform, chlorobenzene and bromobenzene), aromatic hydrocarbons (benzene, toluene, xylene, etc.), aliphatic hydrocarbons (eg For example, chain or cyclic hydrocarbons such as hexane, cyclohexane, octane, and cyclooctane). These aprotic solvents can be used alone or in combination of two or more as a mixed solvent. Among these solvents, polar solvents (tetrahydrofuran, 1,2-dimethoxyethane, etc.) may be used alone or in combination of two or more, and a polar solvent and a nonpolar solvent may be combined.

  Among these aprotic solvents, ethers (tetrahydrofuran, 1,2-dimethoxyethane, bis (2-methoxyethyl) ether, 1,4-dioxane, etc. (especially tetrahydrofuran, 1,2-dimethoxyethane)) are used. It is preferable to use it alone or in combination of two or more or mixed with another solvent.

  In the present invention, the substrate halosilane compound (supporting electrolyte and Mg ion source) is usually dissolved in these aprotic solvents and used for the electrode reaction. In addition, since the halosilane compound reacts rapidly with water, it is preferable that the raw materials to be used (that is, the supporting electrolyte, the Mg ion source, the aprotic solvent, etc.) are dried before use.

(Ratio of each component)
The concentration (substrate concentration) of the halosilane compound in the raw material mixture (reaction solution) is usually about 0.05 to 20 mol / l, preferably about 0.1 to 15 mol / l, more preferably 0.2 to 5 mol / l. Degree. If the substrate concentration is too low, the current efficiency may be reduced, and if it is too high, the supporting electrolyte may not be dissolved.

  The concentration of the supporting electrolyte in the reaction solution can usually be selected from the range of about 0.05 to 4 mol / l, preferably about 0.1 to 3 mol / l, more preferably about 0.15 to 1 mol / l. . If the concentration of the supporting electrolyte is too low, the ionic conductivity that can be provided to the raw material mixture is too low, and the reaction may not proceed sufficiently. If the concentration is too high, the supporting electrolyte may crystallize and precipitate in the reaction solution.

  The concentration of the Mg source in the reaction solution is usually about 0.001 to 0.5 mol / l, preferably about 0.01 to 0.3 mol / l, more preferably about 0.05 to 0.2 mol / l. is there. If the concentration of the Mg source (Mg ions) in the reaction solution is too low, the progress of the reaction may be remarkably slow, and if it is too high, it may crystallize and precipitate in the reaction solution. In addition, the ratio of Mg ion may be about 1 to 10 equivalents, preferably 1 to 5 equivalents, and more preferably about 1 to 3 equivalents with respect to the halogen of the halosilane compound.

(electrode)
The negative anode material in the electrode reaction is not particularly limited, and various conductive electrode materials such as metal materials (SUS (chromium steel), Fe, Ni, Co, Pt, Mg, Cu, Al, Zn, Sn). Etc.), carbon materials, etc. can be used. The cathode material and the anode material can be determined by appropriately selecting from these materials. Of these materials, it is preferable to use at least an anode material that is non-consumable or non-eluting by electricity (a metal material such as SUS or Pt; a carbon material). The anode and the cathode may be formed of the same material or different materials. As a combination of the anode material and the cathode material, for example, (i) a combination of Mg (anode) and Mg, Cu, Zn, Sn, Al, Ni, Co, or a carbon material (cathode), (ii) Cu or Combinations of Al (anode) and Mg, Cu, Al, Ni, Co or Pt (cathode), (iii) combinations of SUS, (iv) combinations of carbon materials, (v) combinations of Pt, etc. Can be mentioned. As the carbon electrode, an artificial graphite electrode, a natural graphite electrode, a self-fired electrode, a carbonaceous electrode, or the like can be used, but usually a graphite electrode is often used.

  In particular, a carbon electrode using a porous carbon material (particularly a fine carbon electrode in the form of needles, fibers, etc.) may be used as at least an anode (usually both positive and negative cathodes) because of its large electrode surface area. .

  Conventionally, it has been necessary to use an easily oxidized material such as Mg or Mg alloy as the anode material. However, in the present invention, by adding Mg ions to the reaction solution, the selection range of the anode can be expanded. it can. In addition, since a non-consumable anode can be used by energization, the electrode reaction can be efficiently performed even in a flow system, and polysilane can be produced.

  In the present invention, the shape of the electrode is not particularly limited, and may be a rod shape, plate shape (disk shape, disk shape, etc.), thin film shape, cylindrical shape, coil shape, needle shape, or fiber shape. Good.

  In the case of an electrode on which an oxide film is easily formed, the oxide film is usually removed and used for the electrode reaction by a removal method suitable for the material. In the case of an electrode formed of a metal material, the oxide film is removed by, for example, a method of cleaning and drying the electrode with an acid, a method of polishing the electrode in an inert gas atmosphere, or a combination of these. be able to.

(Reactor)
In the present invention, polysilane can be produced by continuously performing an electrode reaction using a flow reactor. Therefore, even if Joule heat is generated by energization, it can be efficiently removed, the reaction temperature can be easily controlled, and polysilane with little variation in molecular weight distribution can be obtained.

  The reaction from halosilane to polysilane proceeds on the electrode. Therefore, from the viewpoint of reaction efficiency, a flow-type microreactor is usually used in the present invention.

  The shape of the flow path of the microreactor is not particularly limited, and may be a straight tubular shape or a tubular shape that is at least partially curved. The flow path may meander. The cross-sectional shape of the flow path may be any of a polygonal shape such as a circle, an ellipse, and a square. In order to efficiently bring the reaction liquid into contact with the electrode, in a microreactor, a tubular channel having a rectangular cross section is usually sandwiched between an anode and a cathode in many cases. In terms of the contact efficiency between the reaction solution and the electrode, the flow path often meanders while being in contact with the electrode in the microreactor.

  The average inner diameter of the flow path is not particularly limited, and is, for example, about 1 to 10 mm, preferably about 1.2 to 5 mm, and more preferably about 1.5 to 3 mm.

The electrode reaction is performed by passing a direct current between the electrodes of the microreactor while flowing the reaction solution (raw material mixture) at a constant space velocity (SV). The space velocity may be about ¹ to 10 h ⁻¹ , preferably about 2 to 8 h ⁻¹ , more preferably about 3 to 7 h ⁻¹ . If the space velocity (SV) of the reaction liquid circulation is too slow, there is a risk that the supply of raw materials will be insufficient compared with the progress of the electrode reaction, resulting in a decrease in production, and if it is too fast, the reaction yield may be decreased. There is.

  The energization amount may be, for example, about 0.1 to 5F, preferably about 0.5 to 3F, and usually 1F or more with respect to 1 mol of the halogen atom in the raw material. Note that the molecular weight of the polysilane can be controlled by adjusting the energization amount.

  If necessary, the polarity of the electrodes may be switched as appropriate. Switching may be performed regularly at regular intervals or irregularly. By switching the polarity of the electrodes, it is possible to prevent or reduce the occurrence of a film on the electrode surface due to energization and the increase in electrical resistance.

  The reaction temperature is not particularly limited as long as it is not higher than the boiling point of the aprotic solvent to be used, and may be, for example, 0 to 150 ° C, preferably 5 to 100 ° C, more preferably about 10 to 80 ° C. Since the molecular weight of polysilane changes depending on the reaction temperature, it is preferable to reduce the temperature change during the reaction (for example, within ± 5 ° C.). The reaction temperature may be adjusted, for example, by adjusting the temperature and supply amount of the raw material mixture, the supply rate, the outflow rate of the reaction solution containing the product, and the reaction solution in the reactor may be cooled if necessary. It may be done by doing. If a flow type microreactor is used, the distance between the electrodes is narrow compared to a normal electrolytic cell, and the generation of Joule heat is suppressed, so that it is possible to cool efficiently and temperature control is easy. is there.

  In many cases, the reaction is usually performed in an atmosphere of an inert gas (such as helium, nitrogen, or argon). The reaction is preferably performed in a dry atmosphere. The reaction may be performed under pressure or reduced pressure, but is usually performed at normal pressure.

  In addition, in order to accelerate | stimulate reaction, you may stir the reaction liquid in a reactor suitably. Stirring may be performed by mechanical stirring means or the like, or may be performed by ultrasonic waves.

(Polysilane)
The polymerization form of the polysilane obtained by the production method of the present invention is not particularly limited, and may be a random or block copolymer. The block copolymer can be obtained, for example, by using an oligomer or polymer of the dihalosilane compound (2) (particularly an oligomer or polymer having a large number of repeating dihalosilane units). Further, when the dihalosilane compound (2) is used as a monomer, or an oligomer having a small number of dihalosilane units is used, a random copolymer can be obtained. Furthermore, when the halosilane compound (3) and / or the halosilane compound (4) is used, a polysilane having a crosslinked structure can be obtained. Further, when the monohalosilane compound (1) is reacted with each other, disilane can be obtained.

  The degree of polymerization or the average degree of polymerization of the polysilane may be, for example, 2 to 1000, preferably 5 to 500, and more preferably about 10 to 300.

  The polysilane is, for example, 500 to 20,000, preferably 500 to 15,000 (for example, 1,000 to 10,000), more preferably 2,000 to 8,000 (for example, 3,000 to 7,000). It may have a weight average molecular weight of about). The ratio of the weight average molecular weight (Mw) to the number average molecular weight (Mn) of the polysilane is Mw / Mn = 1 to 2, preferably 1.1 to 1.8, more preferably 1.1 to 1.7. It may be a degree.

  Since the polysilane obtained by the method of the present invention has a high molecular quality with little variation in molecular weight distribution, various applications such as ceramic precursors, photoelectron materials (for example, photoelectrophotographic materials such as photoresists and organic photoreceptors, In addition to an optical transmission material such as an optical waveguide, an optical recording material such as an optical memory, and a material for an electroluminescence element, it can also be used as a flame retardant, a water repellent, a release agent, and the like.

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

Example 1
In a micro flow cell (cell capacity 0.2 ml) equipped with an Mg electrode as an anode and a carbon fiber electrode as a cathode, 1 g of lithium perchlorate, 0.06 g of magnesium chloride, 0.96 g of methylphenyldichlorosilane in a dry nitrogen gas atmosphere, Then, a mixed solution of 10 ml of dry tetrahydrofuran (THF) was passed at a flow rate of 1 ml / h, and a polysilane was synthesized by passing a direct current of 50 mA between the negative and positive electrodes at a temperature of 25 ° C. and atmospheric pressure.

  When the reaction solution discharged from the micro flow cell was analyzed by gel permeation chromatography (GPC), polysilane having a weight average molecular weight Mw of 8500 was obtained at a conversion rate of 95%. The ratio of the weight average molecular weight Mw to the number average molecular weight Mn was Mw / Mn = 1.6.

Example 2
Polysilane was synthesized in the same manner as in Example 1 except that a mixture of methyl phenyldichlorosilane 0.48 g and phenyltrichlorosilane 0.35 g was used instead of 0.96 g of methylphenyldichlorosilane, and the reaction solution was analyzed. . As a result, polysilane having a weight average molecular weight of 4300 was obtained at a conversion rate of 83%.

Example 3
Polysilane was synthesized in the same manner as in Example 1 except that 1.71 g of chlorodimethylphenylsilane was used instead of 0.96 g of methylphenyldichlorosilane, and the reaction solution was analyzed. As a result, 1,2-diphenyl-1,1,2,2-tetramethyldisilane was obtained at a conversion rate of 85%.

Example 4
Polysilane was synthesized in the same manner as in Example 1 except that a carbon fiber electrode was used for both the negative and positive electrodes, and 0.6 g of magnesium chloride was used, and the reaction solution was analyzed. As a result, polysilane having a polymerization average molecular weight of 4800 was obtained at a conversion rate of 90%.

Comparative Example 1
Equipped with three-way cock and two Mg electrodes (1 cm x 1 cm x 5 cm; washed with dilute sulfuric acid, then washed with ethanol and ether, dried under reduced pressure, and polished in a nitrogen atmosphere to remove the oxide film on the surface) In a three-necked flask (reactor) with an internal volume of 30 ml, 0.64 g of anhydrous lithium perchlorate was placed, heated and decompressed, and held at 50 ° C. and 1 mmHg (133.3 Pa) for 6 hours to dry the lithium perchlorate. I let you. Deoxygenated dry nitrogen was introduced into the reactor, and 15 ml of tetrahydrofuran previously dried with sodium-benzophenone ketyl was added. To this mixture, 0.97 ml of methylphenyldichlorosilane previously dried with calcium hydride and distilled was added with a syringe, and the reactor was kept at room temperature on a water bath and energized with a constant voltage power source. The energization takes about 96 hours so that the energization amount is 5.4 F / mol based on the chlorine in methylphenyldichlorosilane while converting the polarity of the two electrodes every minute using a commutator. went.

  After completion of the reaction, 150 ml of 1N (1 mol / l) hydrochloric acid was added to the reaction solution, followed by extraction with ether and reprecipitation of the product with a poor solvent 2-propanol and a good solvent tetrahydrofuran to obtain a polysilane having a weight average molecular weight Mw5540. was gotten. The ratio of the weight average molecular weight Mw to the number average molecular weight Mn was Mw / Mn = 2.5.

Claims (6)

A method for producing polysilane by subjecting a halosilane compound to an electrode reaction, the halosilane compound having a concentration of 0.05 to 20 mol / l, a magnesium ion having a concentration of 0.001 to 0.5 mol / l , and a concentration of 0.05 to A mixture containing 4 mol / l of a perchlorate as a supporting electrolyte and an aprotic solvent was continuously supplied to a flow-through microreactor at a space velocity of ¹ to 10 h ⁻¹ , and a direct current was passed through the mixture. To produce polysilane. A halosilane compound is represented by a monohalosilane compound represented by the following formula (1), a dihalosilane compound represented by the following formula (2), a trihalosilane compound represented by the following formula (3), and the following formula (4). The production method according to claim 1, which is at least one selected from tetrahalosilane compounds.

(Wherein X ^{1 to} X ⁴ are the same or different and each represents a halogen atom, and R ^{1 to} R ³ are the same or different and each represents a hydrogen atom, an organic group or a silyl group)   The production method according to claim 1, wherein at least one selected from dialkylmonoarylmonohalosilane, monoalkylmonoaryldihalosilane and monoaryltrihalosilane is used as the halosilane compound.   A microreactor comprises a mixture comprising a halosilane compound, an alkali metal perchlorate as a supporting electrolyte, a magnesium halide as a magnesium ion source, and at least one aprotic solvent selected from tetrahydrofuran and 1,2-dimethoxyethane The manufacturing method of Claim 1 supplied to.   The production method according to claim 1, wherein at least an anode material is made of a material that is not eluting when energized.   The manufacturing method according to claim 1, wherein the positive electrode is a carbon electrode.