JP2000219744A - Organic/inorganic composite particle, its production, and its use - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain particles having mechanical recovery, hardness, and a breaking strength by selecting particles containing an organic polymer skeleton and a polysiloxane skeleton having an organosilicon bonded to at least one carbon atom of the organic polymer skeleton and having a specified amount or larger amount of SiO2 units constituting the skeleton and having a specified mean particle diameter. SOLUTION: Composite particles are provided each of which contains an organic polymer skeleton and a polysiloxane skeleton having in the molecule an organic silicon directly bonded to carbon atoms of the organic polymer skeleton and in each of which the content of SiO2 units constituting the polysiloxane skeleton is at least 25 wt.%. The particles have a mean particle diameter of at least 0.5 μm, a coefficient of variation of at most 20%, a compressive modulus of 350-3,000 kg/mm2, and a breaking strength G (kg) in the range: G>=1.4Y1.75 (wherein Y is a particle diameter). They are obtained by hydrolytically condensing a silicon compound represented by formula I or the like in a water/organic solvent mixture, forming a polymer skeleton by a radical polymerization reaction in the presence of a radical polymerization initiator, and heat-treating the entire at 100-600 deg.C. In the formula, R1 is hydrogen or methyl; R2 is a 1-20C divalent organic group; and R3 is a 1-5C alkyl or the like.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

The present invention relates to organic-inorganic composite particles and a method for producing the same.

[0002]

2. Description of the Related Art A liquid crystal display (LCD) comprises two opposing electrode substrates, a spacer interposed between the electrode substrates, and a liquid crystal material. The spacer is used to keep the thickness of the liquid crystal layer uniform and constant. In general, high-speed response, high contrast, wide viewing angle, and the like can be cited as display performance required for practical use of a liquid crystal display panel. In order to realize these various performances, the thickness of the liquid crystal layer, that is, the gap distance between the two electrode substrates must be kept strictly constant.

As a spacer for a liquid crystal display panel meeting such a demand, silica particles produced by a sol-gel method (Japanese Patent Application Laid-Open No. 62-269933) and those obtained by calcining the silica particles (Japanese Patent Application Laid-Open No. 234826) and styrene-based and divinylbenzene-based polymer particles obtained by suspension polymerization of styrene-based monomers and divinylbenzene-based monomers (Japanese Patent Application Laid-Open No. 61-95016).
These are spherical particles having a narrow particle diameter distribution and a uniform particle diameter. However, the above-described related art has the following problems. (A) Since the silica particles produced by the sol-gel method are calcined and have poor deformability and are very hard, when pressed to produce a liquid crystal display panel, a vapor deposition layer such as an electrode on a substrate is formed. This causes physical damage to a coating layer such as an alignment film and a color filter, causing image defects and pixel defects due to TFT disconnection. Further, since the difference in the thermal expansion coefficient between the calcined silica particles and the liquid crystal is large, when the liquid crystal display panel using the calcined silica particles is exposed to a low temperature environment of, for example, −40 ° C., the liquid crystal shrinks. Does not shrink,
There is a problem of so-called low-temperature bubbling, in which a gap is formed between the liquid crystal layer and the electrode substrate and the display function does not operate at all. (B) Silica particles produced by the sol-gel method are softer than calcined silica particles. However, since the unsintered silica particles are inferior in mechanical resilience, the gap distances become non-uniform and image unevenness is likely to occur. In addition, unfired silica particles cause a problem of low-temperature foaming similarly to fired silica particles. (C) Styrene-based or divinylbenzene-based polymer particles are organic particles and are very soft, so the number of sprayed particles must be increased. This not only increases the manufacturing cost, but also increases the area of the part where no image is formed. Furthermore, an increase in the amount of impurities such as ions and molecules eluting from the inside of the spacer into the liquid crystal layer causes deterioration in various display qualities such as a decrease in contrast and an increase in roughness.

Accordingly, polymer particles have been proposed which are hardly deformed by using a large amount of a crosslinkable monomer such as divinylbenzene or by carrying out suspension polymerization using a large amount of a polymerization initiator (JP-A-4-313727). No.). Also,
There has been proposed a polymer particle in which tetramethylolmethane tetraacrylate or tetramethylolmethanetetraacrylate and divinylbenzene are subjected to suspension polymerization and then the average particle diameter and the standard deviation are adjusted by classification (Japanese Patent Application Laid-Open No. 6-503180). ). These polymer particles have a problem that abnormal alignment of the liquid crystal easily occurs. In the liquid crystal display panel, display cannot be performed at a portion where abnormal liquid crystal orientation occurs.

The present inventors have developed a 10% compression modulus and 10%
Japanese Patent Application No. 5-288536 proposes a spacer for a liquid crystal display panel in which the residual displacement after deformation is in a specific range and is composed of specific organic-inorganic composite particles. Since the liquid crystal display panel spacer has a higher hardness than conventional polymer particles, the number of sprayed particles can be reduced. However, reducing the number of sprays increases the load applied to each particle, so that the breaking strength may be insufficient. Conventional conductive particles include inorganic compound particles such as silica particles or polymer particles and a conductive layer formed on the surface of the particles. Generally, conductive particles are used in the electronics packaging field to connect between a pair of electrodes. That is, a pair of electrodes with the conductive particles interposed therebetween is pressed to electrically connect the two electrodes via the conductive particles.

When the conductive particles contain polymer particles, the conductive layer is too soft, so that the conductive layer cannot follow the deformation of the particles at the time of pressurization, and the conductive layer peels off from the particle surface or the electrodes are too stuck to each other to cause a short circuit. Or On the other hand, when the conductive particles contain inorganic compound particles, they are too hard, so that the contact area with the electrode is not widened, the contact resistance value cannot be reduced, or the conductive layer is subjected to excessive pressure during deformation. May come off. Further, if the mechanical restorability of the conductive particles is poor, it is difficult to keep the gap distance constant, and there is a problem that a contact failure occurs.

[0007]

SUMMARY OF THE INVENTION It is an object of the present invention to provide a mechanical restoration required for maintaining a constant gap distance between a pair of members to be arranged at a precise distance and a small number of the gaps. It is an object of the present invention to provide organic-inorganic composite particles having hardness and breaking strength necessary for maintaining a constant distance and hardly causing physical damage to the member. Another object of the present invention is to maintain a constant gap distance between a pair of members to be arranged at a precise distance, and to maintain the gap distance constant with a small number of members. Another object of the present invention is to provide a method for producing organic-inorganic composite particles having the hardness and breaking strength required for the above-mentioned method and the organic-inorganic composite particles hardly causing physical damage to the member.

[0008]

Means for Solving the Problems The organic-inorganic composite particles of the present invention contain an organic polymer skeleton and a polysiloxane skeleton. The polysiloxane skeleton has in its molecule an organosilicon in which a silicon atom is chemically bonded directly to at least one carbon atom in the organic polymer skeleton. The amount of SiO ₂ constituting the polysiloxane skeleton is 25% based on the total weight of the particles.
wt% or more. The average particle size is 0.5 μm or more, and the following formula:

[0009]

(Equation 2)

(Where G indicates breaking strength [kg]; Y
Represents a particle diameter [mm]). In the organic-inorganic composite particles of the present invention, for example, the coefficient of variation of the particle diameter is 20% or less. Further, for example, the 10% compression modulus is 350 to 3000 kg / mm ² . The organic-inorganic composite particles of the present invention may be colored by containing at least one selected from the group consisting of dyes and pigments. The method for producing organic-inorganic composite particles of the present invention includes a condensation step, a polymerization step, and a heat treatment step.

The condensation step is a step of hydrolyzing and condensing using the first silicon compound having a radical polymerizable group.
The first silicon compound has the following general formula 1:

[0012]

Embedded image

(Wherein, R ¹ represents a hydrogen atom or a methyl group; R ² has 1 to 5 carbon atoms which may have a substituent)
R ³ represents at least one monovalent group selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, and an acyl group having 2 to 5 carbon atoms; Show)
And the following general formula 2:

[0014]

Embedded image

(Wherein R ⁴ represents a hydrogen atom or a methyl group; R ⁵ is selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, and an acyl group having 2 to 5 carbon atoms) At least one monovalent group), and the following general formula 3:

[0016]

Embedded image

(Wherein R ⁶ represents a hydrogen atom or a methyl group; R ⁷ has 1 to 5 carbon atoms which may have a substituent)
R ⁸ represents at least one monovalent group selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, and an acyl group having 2 to 5 carbon atoms; Show)
And at least one selected from the group consisting of compounds represented by at least one general formula selected from the group consisting of: and derivatives thereof. The polymerization step is a step in which a radical polymerizable group undergoes a radical polymerization reaction during and / or after the condensation step.

The heat treatment step is a step of heat treating the polymer particles produced in the polymerization step at a temperature of 100 ° C. to 600 ° C. In the production method of the present invention, the condensation step, together with the radical polymerizable group-containing first silicon compound, if necessary,
General formula 5

[0019]

Embedded image

(Where X is CH ₂ ＣC (-R ¹ ) -C
_{^{OOR 2 -, CH 2 = C}} (-R 4) - , or CH ₂ = C (-
R ⁶ ) represents a monovalent radical polymerizable functional group represented by —R ⁷ —; R ¹ , R ⁴ and R ⁶ represent a hydrogen atom or a methyl group; R ² and R ⁷ have a substituent. Carbon number 1 that may be
Represents a divalent organic group having from 20 to 20; R ⁹ represents at least one monovalent group selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, and an acyl group having 2 to 5 carbon atoms; R ¹⁰ represents an optionally substituted carbon number of 1 to 10
And at least one monovalent group selected from the group consisting of an alkyl group having 6 to 10 carbon atoms; m represents an integer of 2 to 3; n represents an integer of 0 to 2;
Represents an integer of 2 to 3. A plurality of Xs may be different from each other, or two or more may be the same. when n is 2, to the two R ¹⁰ may be different from each other, it may be the same. For 4-m-n is 2, the two R ⁹ are may be different from each other, at least one selected from the compounds represented by either the same or) and the group consisting of a derivative thereof, the radical Hydrolysis / condensation is performed using a polymerizable group-containing second silicon compound, and without using a radical polymerizable monomer other than the radical polymerizable group-containing first silicon compound and the radical polymerizable group-containing second silicon compound. It may be something.

In the manufacturing method of the present invention, the heat treatment step
It may be performed in a vacuum at a temperature of 00 ° C. or less. In the production method of the present invention, the condensation step uses a radically polymerizable group-containing second silicon compound as necessary to form a hydrolyzable and condensable metal compound other than the radically polymerizable group-containing first and second silicon compounds. The heat treatment process may be performed at a temperature of 800 ° C. or less with respect to the total weight of the first and second silicon compounds. In the production method of the present invention, the condensation step uses a radical polymerizable group-containing second silicon compound as necessary, and converts the radical polymerizable monomer other than the radical polymerizable group-containing first and second silicon compounds into the first silicon compound. And the heat treatment step may be performed at a temperature of 800 ° C. or less based on the total weight of the second silicon compound.

[0022]

Means for Solving the Problems [Organic-inorganic composite particles
The organic-inorganic composite particles of the present invention are organic polymer
At least one carbon atom in the skeleton and the organic polymer skeleton
Organic silicon in which silicon atoms are directly chemically bonded
Having a polysiloxane skeleton and having a polysiloxane bone
SiO constituting the case _TwoIs more than 25wt%
With the large hardness characteristic of the polysiloxane skeleton,
Mechanical resilience and fracture characteristic of organic polymer backbone
Breaking strength. Therefore, the organic-inorganic composite of the present invention
The coalesced particles are placed between a pair of members that must be precisely spaced.
Mechanical resilience required to maintain a constant gap distance
In order to keep the gap distance constant with a small number of
With the required hardness and breaking strength
It is hard to cause physical damage to members. And the book
The organic-inorganic composite particles of the present invention have a thickness of 0.5 μm or more.
Since it has a uniform particle size, a gap is formed between a pair of members
Useful for

The organic polymer skeleton contains at least the main chain of the main chain, side chain, branched chain and crosslinked chain derived from the organic polymer. The molecular weight, composition, structure, presence or absence of a functional group, and the like of the organic polymer are not particularly limited. The organic polymer is, for example, at least one selected from the group consisting of (meth) acrylic resin, polystyrene, polyvinyl chloride, polyvinyl acetate, polyolefin, and polyester. Preferred organic polymer backbones have repeating units -C because they form particles with particularly good mechanical resilience.
-Having a main chain composed of -C-
"Vinyl-based polymer").

The vinyl polymer is, for example, (meth)
It is at least one selected from the group consisting of acrylic resin, polystyrene, polyvinyl chloride, polyvinyl acetate, and polyolefin. Preferred vinyl polymers are at least one selected from the group consisting of (meth) acrylic resins, (meth) acryl-styrene resins, and polystyrene. More preferred vinyl polymers are (meth) acrylic resins and (meth) acryl-styrene resins. The polysiloxane has the following formula 4:

[0025]

Embedded image

A siloxane unit represented by the following formula is defined as a compound which forms a three-dimensional network by continuous chemical bonding. The silicon atom in the polysiloxane is directly chemically bonded to at least one of the carbon atoms constituting the organic polymer skeleton. Si constituting the polysiloxane skeleton
The amount of O ₂ is at least 25 wt%, preferably 30 to 80 wt%, based on the weight of the organic-inorganic composite particles of the present invention.
%, More preferably 33 to 70 wt%, and most preferably 37 to 60 wt%. When the content is in the above range, the particles have an effective hardness, mechanical resilience, and breaking strength. If it is less than 25 wt%, there is a problem that hardness, which is a characteristic of inorganic materials, is not exhibited, and a 10% compression elastic modulus described later is small. If it exceeds the above range, the mechanical resilience or the breaking strength of the organic polymer skeleton is impaired, and the residual displacement may be increased or the particles may be broken.

The amount of SiO ₂ constituting the polysiloxane skeleton is a percentage by weight determined by measuring the weight before and after firing the particles at a temperature of 1000 ° C. or more in an oxidizing atmosphere such as air. The organic-inorganic composite particles of the present invention can contain an inorganic component other than polysiloxane. Inorganic components other than polysiloxane, for example,
Oxides such as boron, aluminum, titanium, and zirconium. The amount of inorganic components other than polysiloxane is 0
-20 wt% is preferable, and 0-10 wt% is more preferable. If the ratio is out of the above range, the hardness, mechanical resilience, or breaking strength may not be effectively exhibited.

The organic-inorganic composite particles of the present invention have a particle size of 0.1.
It has an average particle diameter of 5 μm or more, preferably 0.5 to 5
It has an average particle size of 0 μm, more preferably 1-25 μm, more preferably 1.5-20 μm. 0.5 μm
Below, it is difficult to form a gap between the pair of members. Outside the above range, the region is not used as a spacer for a liquid crystal display panel and as a conductive particle. When the organic-inorganic composite particles of the present invention are used as a spacer, the coefficient of variation of the particle diameter is, for example, 20% or less, preferably 10% or less, more preferably 8% or less from the viewpoint of uniformity of the gap distance between the electrode substrates. Having. If the upper limit is exceeded, the uniformity of the gap distance is reduced and image unevenness is likely to occur. The coefficient of variation of the particle size is given by:

[0029]

(Equation 3)

Is defined as In the present invention, the average particle diameter and the standard deviation between the particle diameters are calculated for any particle 2 in an electron micrograph.
The particle diameter of 00 particles was actually measured and determined by the following equation.

[0031]

(Equation 4)

The organic-inorganic composite particles of the present invention contain both the inorganic structural unit represented by the above formula (4) and the organic polymer skeleton, and the inorganic structural unit and the organic polymer skeleton are chemically bonded. Particles. Therefore, the organic-inorganic composite particles of the present invention have both high hardness, which is a characteristic of an inorganic substance, and high mechanical resilience and breaking strength, which are characteristics of an organic polymer. The scale indicating hardness is 1
It is 0% compression modulus, and the scale showing mechanical resilience is 1
This is the residual displacement after 0% deformation. Here, the 10% compression modulus is a value measured by the following measurement method. Shimadzu Micro Compression Testing Machine (MCTM-200 manufactured by Shimadzu Corporation)
At room temperature (25 ° C), the sample stage (material: SK
(S plate), one sample particle sprayed on the
Using a μm circular flat indenter (material: diamond)
A load is applied at a constant load speed in the direction of the center of the particles, and the particles are deformed until the compressive displacement becomes 10% of the particle diameter.
Calculate the number of millimeters of the load and compressive displacement during deformation. The obtained compression load, particle compression displacement, and particle radius are expressed by the following equations:

[0033]

(Equation 5)

[Where E: compression modulus (kg / mm ² ) F: compression load (kg) K: Poisson's ratio of particles (constant, 0.38) S: compression displacement (mm) R: radius of particles (Mm). ] Is 10% compression elastic modulus. Immediately thereafter, immediately after removing the load at the same speed as when the load was applied, the load was unloaded until the load became 0.1 g, and the load-displacement curve was extrapolated along the tangent line so that the load finally became 0 g. The displacement still remaining on the particles is determined. The residual displacement is calculated as a percentage of the particle diameter. This operation is performed for three different particles, and the average value is defined as the 10% compression modulus and the residual displacement of the particles, which are used as a measure of the hardness and the mechanical resilience of the particles, respectively.

The breaking strength can be checked by using the above-mentioned micro compression tester. As described above, a load is applied to one sample particle spread on the sample stage in the direction of the center of the particle using a circular flat indenter at a constant speed, and the compression load at which the particle is broken can be obtained. When the 10% compression modulus of the particles used as the conventional spacer was measured by the above-mentioned measuring method, the calcined silica particles were 4400 kg / mm ² , and the styrene-based polymer particles were 300 kg.
/ Mm ² . In contrast, the organic-inorganic composite particles of the present invention have a 10% compression modulus, preferably 350 to
3000 kg / mm ² , more preferably 400 to 25
00 kg / mm ² , even more preferably 500-20
The hardness is adjusted to an arbitrary hardness in the range of 00 kg / mm ² . 1
When the 0% compression modulus falls below the above range, as described above,
When used as a spacer for a liquid crystal display panel, there is a risk of an increase in manufacturing cost due to an increase in the number of scattered particles, a decrease in contrast, and an increase in roughness. Physical damage and low temperature foaming.

Regarding the residual displacement after 10% deformation, the unsintered silica particles had a residual displacement of 8%, but the organic-inorganic composite particles of the present invention preferably had a residual displacement of 0 to 5%, more preferably. Is 0-4%, more preferably 0-3%
It is a composite particle having a residual displacement in the range of and excellent in mechanical restorability. If the residual displacement after 10% deformation exceeds the above range, image unevenness is likely to occur when used as a spacer for a liquid crystal display panel. As for the breaking strength, the organic-inorganic composite particles of the present invention have the following formula:

[0037]

(Equation 6)

(Where G and Y are as described above), preferably by the following formula:

[0039]

(Equation 7)

(Here, G and Y are as described above.) If the breaking strength does not satisfy the above formula, the breaking strength may be so small that the particles may be broken at the time of manufacturing the liquid crystal display panel, and the gap distance between the electrode substrates cannot be kept constant. The 10% compression modulus and the degree of residual displacement in the above range can be achieved by adjusting the amount of the polysiloxane skeleton or the organic polymer skeleton in the particles. For example, when the amount of the polysiloxane skeleton is reduced, the 10% compression modulus and the residual displacement are reduced, and when the amount of the polysiloxane skeleton is increased,
10% compressive modulus and residual displacement increase.

The organic-inorganic composite particles of the present invention may be colored by containing at least one selected from the group consisting of dyes and pigments. The color of the particles is preferably a color that does not transmit light. A color that does not transmit light is preferable as a color of the spacer for the liquid crystal display panel because light leakage can be prevented and image quality contrast can be improved. Colors that do not transmit light include colors such as black, dark blue, dark blue, dark blue, purple, blue, dark green, green, brown, and red, with black, dark blue, and dark blue being particularly preferred. The dye is appropriately selected and used according to the color to be colored, and examples thereof include disperse dyes, acid dyes, basic dyes, reactive dyes, sulfur dyes, and the like, classified according to the dyeing method. Specific examples of these dyes are described in “Chemical Handbook Applied Chemistry, edited by The Chemical Society of Japan” (1986, published by Maruzen Co., Ltd.), pp. 1399-1427, and “Nippon Kayaku Dye Handbook” (published, 1973 by Nippon Kayaku Co., Ltd.). )It is described in.

The method for dyeing the organic-inorganic composite particles of the present invention may be a conventionally known method. For example, it can be carried out by the method described in the above-mentioned “Chemical Handbook Applied Chemistry Edition, The Chemical Society of Japan” or “Nippon Kayaku Dye Handbook”. The dyed organic-inorganic composite particles of the present invention have both the above-mentioned hardness and mechanical resilience, and are particularly useful for improving the image quality of a liquid crystal display panel. Preferred embodiments when the organic-inorganic composite particles of the present invention are used as a spacer for a liquid crystal display panel are as follows. The breaking strength G satisfies Equation 6 above, and more preferably Equation 7 above.

The amount of the polysiloxane skeleton is at least 25 wt%, the 10% compression modulus is 350 to 3000 kg / mm ² ,
% Residual displacement after deformation 0-5%, average particle size 0.5-50
μm and the coefficient of variation of the particle diameter is 20% or less. Amount of polysiloxane skeleton 30-80 wt%, 10%
Compression elastic modulus 400 to 2900 kg / mm ² , residual displacement after 10% deformation 0 to 4%, average particle diameter 1 to 25 μm, and
The coefficient of variation of the particle diameter is 10% or less. Amount of polysiloxane skeleton 33-70 wt%, 10%
The compression elastic modulus is 500 to 2800 kg / mm ² , the residual displacement after 10% deformation is 0 to 3%, the average particle size is 1.5 to 20 μm, and the variation coefficient of the particle size is 8% or less.

Amount of polysiloxane skeleton 37-60 w
t%, 10% compression modulus 550-2700 kg / mm ² , 1
Residual displacement after 0% deformation 0-2%, average particle size 2-15μ
m and the variation coefficient of the particle diameter are 6% or less. In the above, the breaking strength G and the above equation 6
More preferably, the above expression 7 is satisfied. In any of the above, coloring is carried out by including at least one selected from the group consisting of dyes and pigments. The shape of the organic-inorganic composite particles of the present invention is spherical,
Any particle shape such as needle-like, plate-like, scale-like, crushed, bale-like, cocoon-like, confetti-like, etc. may be used, and is not particularly limited, but when used as a spacer for a liquid crystal display panel, the gap distance is uniformly constant. The shape is preferably spherical. This is because particles that are spherical have a constant or nearly constant particle size in all or almost all directions.

The organic-inorganic composite particles of the present invention can be produced, for example, by the method for producing the organic-inorganic composite particles of the present invention described below, but may be produced by other production methods. [Method for Producing Organic-Inorganic Composite Particles] The method for producing organic-inorganic composite particles of the present invention includes a condensation step, a polymerization step, and a heat treatment step. The condensation step is a step of performing hydrolysis and condensation using the first silicon compound. The first silicon compound is at least one selected from the group consisting of compounds represented by at least one general formula selected from the group consisting of general formulas 1, 2 and 3 and derivatives thereof.

In the condensation step, the first silicon compound and the second silicon compound
Both silicon compounds can be used. The second silicon compound is at least one selected from the group consisting of the compound represented by the above general formula 5 and a derivative thereof. In the general formulas 1 to 3, and 5, the radical polymerizable group is CH ₂ ＣC (—R ¹ ) —COOR ² —, CH ₂ ＣC
(—R ⁴ ) — or CH ₂ ＣC (—R ⁶ ) —R ⁷ —. In general formula 5, when there are two or more radically polymerizable groups, they may be different from each other, or two or more may be the same. By subjecting the radical polymerizable group to a radical polymerization reaction, an organic polymer skeleton derived from the vinyl polymer described above is generated. The radical polymerizable group includes an acryloxy group (when R ¹ is a hydrogen atom in general formulas 1 and 5), a methacryloxy group (when R ¹ is a methyl group in general formulas 1 and 5), and a vinyl group (when general formula 2 is a general formula 2). And when R ⁴ is a hydrogen atom in formulas 5 and 5, an isopropenyl group (R in formulas 2 and 5)
⁴ is a methyl group), a 1-alkenyl group or a vinylphenyl group (when R ⁶ is a hydrogen atom in the general formulas 3 and 5), or an isoalkenyl group or an isopropenylphenyl group (the general formulas 3 and 5) In which R ⁶ is a methyl group).

In the general formulas 1 to 3, and 5
The functional group is R^ThreeO, R^FiveO, R⁸O and R⁹O. R^ThreeO
Group, R^FiveO group, R⁸O group and R⁹O groups are hydroxyl and carbon
An alkoxy group having 1 to 5 carbon atoms and an acyloxy having 2 to 5 carbon atoms
And a monovalent group selected from the group consisting of General formula 1
3, three R^ThreeO group, three R^FiveO group and R ⁸
The O groups may be different from each other,
The above may be the same. In the general formula 5, R⁹O
When there are two groups, they may be different from each other,
It may be the same. Preferred R^ThreeO group ・ R^FiveO group ・ R⁸
O group ・ R⁹The O group has a high hydrolysis / condensation rate,
Methoxy, ethoxy, propoxy and acetoxy
Selected from the group consisting of
And ethoxy groups are more preferred. First silicon compound
And the second silicon compound are R^ThreeO group ・ R^FiveO group ・ R⁸O
Group R⁹O group hydrolyzed by water and further condensed
To form the polysiloxane skeleton represented by the general formula 4
Form.

In the general formulas 1 to 3 and 5, the R ² and R ⁷ groups have 1 to 2 carbon atoms which may have a substituent.
0 is a divalent organic group. As the divalent organic group,
Although not particularly limited, for example, an alkylene group such as an ethylene group, a propylene group, a butylene group, a hexylene group, an octylene group, which may have a substituent, a phenylene group which may have a substituent, or Examples thereof include a group in which an alkylene group or a phenylene group which may have a substituent is bonded via an ether bond. It is preferable that R ² and R ⁷ have a radical polymerizable group in which R ² and R ⁷ are a propylene group or a phenylene group because they are easily available.

In the general formula 5, the R ¹⁰ group is an alkyl group or an aryl group bonded to a silicon atom. This alkyl group has 1 to 1 carbon atoms which may have a substituent.
It is an alkyl group of 0, for example, a methyl group, an ethyl group, a propyl group, a butyl group, a hexyl group and the like. The aryl group is an aryl group having 6 to 10 carbon atoms, such as a phenyl group and a tolyl group. In the general formula 5, when there are two R ¹⁰ groups, they may be different from each other or may be the same. The compound represented by at least one general formula selected from the group consisting of general formulas 1, 2 and 3 has one silicon atom, three hydrolyzable groups bonded to the silicon atom, It has one bonded radically polymerizable group.

A specific example of the compound represented by the general formula 1 is γ
-Methacryloxypropyltrimethoxysilane, γ-methacryloxypropyltriethoxysilane, γ-acryloxypropyltrimethoxysilane, γ-acryloxypropyltriethoxysilane, γ-methacryloxypropyltriacetoxysilane, γ-methacryloxyethoxypropyl Trimethoxysilane (or also γ-trimethoxysilylpropyl-β-methacryloxyethyl ether), and any one of these may be used alone or two or more of them may be used in combination. Specific examples of the compound represented by the general formula 2 are vinyltrimethoxysilane, vinyltriethoxysilane, vinyltriacetoxysilane, and the like. Any one of these may be used alone, or two or more may be used in combination. Or

A specific example of the compound represented by the general formula 3 is 1
-Hexenyltrimethoxysilane, 1-octenyltrimethoxysilane, 1-decenyltrimethoxysilane, γ
-Trimethoxysilylpropyl vinyl ether, ω-trimethoxysilylundecanoic acid vinyl ester, p-trimethoxysilylstyrene, and the like. Any one of these may be used alone, or two or more thereof may be used in combination. Derivatives of the compounds represented by the general formulas 1 to 3 include, for example, some R ³ O groups of the compounds represented by the general formulas 1 to 3 form β-dicarbonyl groups and / or other chelate compounds. At least one selected from the group consisting of a compound substituted with a group capable of being formed and a compound represented by general formulas 1 to 3 and / or a low-condensate obtained by partially hydrolyzing and condensing the chelate compound thereof. One.

As the first silicon compound, a compound represented by the general formula 1 is preferable because it is easy to form organic-inorganic composite particles having a sharp particle size distribution, and γ-methacryloxypropyltrimethoxysilane,
γ-methacryloxypropyltriethoxysilane, γ-
At least one selected from the group consisting of acryloxypropyltrimethoxysilane and γ-acryloxypropyltriethoxysilane is particularly preferred. The compounds represented by the general formula 5 are the following five. (1) One silicon atom, one radical polymerizable group bonded to a silicon atom, one alkyl group or aryl group bonded to a silicon atom, and two hydrolyzable groups bonded to a silicon atom (M = 1, n = 1). Specific examples of this compound include γ-methacryloxypropylmethyldimethoxysilane, γ-methacryloxypropylmethyldiethoxysilane, γ-acryloxypropylmethyldimethoxysilane, γ-acryloxypropylmethyldiethoxysilane, vinylmethyldimethoxysilane, Vinylmethyldiethoxysilane and the like, any one of which is used alone, or two or more of which are used in combination. (2) One silicon atom, one radical polymerizable group bonded to the silicon atom, two alkyl groups and / or aryl groups bonded to the silicon atom, and one Having a hydrolyzable group (m = 1, n =
2). Specific examples of this compound include γ-methacryloxypropyldimethylmethoxysilane, γ-methacryloxypropyldimethylethoxysilane, γ-acryloxypropyldimethylmethoxysilane, γ-acryloxypropyldimethylethoxysilane, vinyldimethylmethoxysilane and the like. Any one of them may be used alone, or two or more may be used in combination. (3) It has one silicon atom, two radically polymerizable groups bonded to the silicon atom, and two hydrolyzable groups bonded to the silicon atom (m = 2, n = 0). Specific examples of this compound include bis (γ-acryloxypropyl) dimethoxysilane, bis (γ-methacryloxypropyl) dimethoxysilane, and any one of them is used alone, or two or more are used in combination. I do. (4) One silicon atom, two radically polymerizable groups bonded to the silicon atom, one alkyl group or aryl group bonded to the silicon atom, and one hydrolyzable group bonded to the silicon atom (M = 2, n = 1). A specific example of this compound is bis (γ-methacryloxypropyl)
Methylmethoxysilane, bis (γ-acryloxypropyl) methylmethoxysilane and the like, one of which is used alone or two or more are used in combination. (5) It has one silicon atom, three radically polymerizable groups bonded to the silicon atom, and one hydrolyzable group bonded to the silicon atom (m = 3, n = 0). Specific examples of this compound include tris (γ-methacryloxypropyl) methoxysilane, tris (γ-acryloxypropyl) methoxysilane, and the like. One of these compounds is used alone, or two or more are used in combination. I do.

As the second silicon compound, among the compounds represented by the general formula 5, from the viewpoint that it is easy to form organic-inorganic composite particles having a sharp particle size distribution,
When the radical polymerizable group is CH ₂ ＣC (—R ¹ ) —COOR ² —
Compounds that are groups are preferred. The derivative of the compound represented by the general formula 5 is, for example, a group in which some R ⁹ O groups of the compound represented by the general formula 5 can form a β-dicarbonyl group and / or another chelate compound. It is at least one selected from the group consisting of a substituted compound and a low condensate obtained by partially hydrolyzing and condensing a compound represented by the general formula 5 and / or a chelate compound thereof.

When the second silicon compound is hydrolyzed and condensed without using the first silicon compound, the hardness of the obtained particles tends to decrease.
Silicon compounds must be used. In order to obtain the organic-inorganic composite particles of the present invention, in addition to the above-mentioned first and second silicon compounds, silane compounds represented by the following general formulas 6 and 7; derivatives thereof; boron, aluminum, gallium, indium, phosphorus At least one hydrolyzable / condensable metal compound selected from the group consisting of organometallic compounds such as titanium, zirconium and the like and inorganic metal compounds may be used in combination.

[0055]

Embedded image

(Wherein R ¹¹ , R ¹³ and R ¹⁷ are the same as R ³ ; R ¹² , R ¹⁴ and R ¹⁶ are the same as R ¹⁰ ;
¹⁵ is the same as R ⁷ ; p, q and r are 0 or 1.) R ¹¹ and R of the silane compound represented by the general formulas 6 and 7
^{As the} groups ¹³ and R ¹⁷ , a methyl group or an ethyl group is preferred in view of a high hydrolysis condensation rate. p, q, and r are 0 or 1
However, p, q, and r = 0 are preferable in that the hardness of the obtained organic-inorganic composite particles can be increased. Examples of the silane compound represented by the general formula 7 include 1,2-bis (trimethoxysilyl) ethane, 1,2-bis (triethoxysilyl) ethane, and 1-trimethoxysilyl-2.
-Triethoxysilylethane and the like.

The derivatives of the silane compounds represented by the general formulas 6 and 7 have a structure in which some of the R ¹¹ O, R ¹³ O and R ¹⁷ O groups of the compounds represented by the general formulas 6 and 7 are β-dicarbonyl. A compound substituted with a group capable of forming a group and / or another chelate compound and a compound represented by the general formulas 6 and 7 and / or a chelate compound obtained by partially hydrolyzing / condensing the compound. And at least one selected from the group consisting of condensates. The amount of the metal compound that can be hydrolyzed and condensed other than the first and second silicon compounds is not particularly limited, but when used in a large amount, the shape of the organic-inorganic composite particles obtained does not become spherical or the particle diameter is controlled. And the particle size distribution is widened, and thus it may not be suitable for a spacer for a liquid crystal display panel. Therefore, the amount of the metal compound that can be hydrolyzed and condensed is preferably 200 wt% or less, more preferably 100 wt% or less, and more preferably 50 wt%, based on the total weight of the first and second silicon compounds.
% Or less is still more preferred.

The first silicon compound and the second silicon compound and / or a metal compound which can be hydrolyzed and condensed as required (hereinafter, sometimes referred to as “raw material”) contain water. It is hydrolyzed and condensed in a solvent. The hydrolysis and condensation can be performed by any method such as batch, division, and continuous. For hydrolysis and condensation, a catalyst such as ammonia, urea, ethanolamine, tetramethylammonium hydroxide, an alkali metal hydroxide, or an alkaline earth metal hydroxide may be used. Further, an organic solvent other than water and a catalyst may be present in the solvent. Specific examples of the organic solvent include methanol, ethanol, isopropanol, n-butanol,
Alcohols such as isobutanol, sec-butanol, t-butanol, pentanol, ethylene glycol, propylene glycol, and 1,4-butanediol;
Ketones such as acetone and methyl ethyl ketone; esters such as ethyl acetate; (cyclo) paraffins such as isooctane and cyclohexane; ethers such as dioxane and diethyl ether; aromatic hydrocarbons such as benzene and toluene; Alternatively, they are used as a mixture.

The hydrolysis and condensation are carried out, for example, by adding the above-mentioned raw material or its organic solvent solution to a solvent containing water,
To 100 ° C., preferably 0 to 70 ° C. for 30 minutes to 1
It is performed by stirring for 00 hours. Further, the particles obtained by the above method may be charged in a synthesis system in advance as seed particles, and the seed material may be added to grow the seed particles. Thus, the raw material is hydrolyzed and condensed in a solvent containing water under appropriate conditions, whereby particles are precipitated and a slurry is formed. Since the precipitated particles are obtained by hydrolyzing and condensing the above-mentioned silicon compound having a radical polymerizable group, the particles have an arbitrary particle diameter of 0.5 μm or more and have a sharp particle size distribution. Here, the appropriate conditions include, for example, preferably a raw material concentration of 20% by weight or less, a water concentration of 50% by weight or more, and a catalyst concentration of 10% by weight or less based on the obtained slurry.

The average particle size of the particles formed by hydrolysis / condensation can be determined by, for example, the concentration of water, the concentration of the catalyst, the concentration of the organic solvent, the concentration of the raw material, the time of addition of the raw material, the temperature, and the concentration of the seed particles. .99% by weight, 0.01 to 10% by weight, 0 to 90% by weight, 0.1 to 30% by weight, 0.001%
By setting the temperature to 0 to 100 ° C. and 0 to 10% by weight for 500 hours, the average particle size of the organic-inorganic composite particles of the present invention can be set within the above-mentioned range. The coefficient of variation of the particle diameter of the particles to be generated is such that the water concentration, the catalyst concentration, and the organic solvent concentration are set within the above ranges, respectively, so that the organic-inorganic composite particles of the present invention have the above-mentioned variation in particle diameter. It can be within the range of the coefficients.

Further, when the first silicon compound is hydrolyzed and condensed with the second silicon compound and / or a metal compound which can be hydrolyzed and condensed as required, the average particle diameter is 0.4 μm or less. It is preferable to further use inorganic fine particles. This is because the obtained organic-inorganic composite particles have higher hardness and improved breaking strength by containing the inorganic fine particles chemically bonded to the polysiloxane skeleton. Specific examples of the inorganic fine particles include, for example, silica, alumina, aluminum hydroxide, titanium oxide, and zirconium oxide.Silica is preferred because it is easily introduced into particles obtained by hydrolyzing and condensing a raw material. .

The average particle size of the inorganic fine particles is 0.4 μm
It is not preferable that the amount exceeds the range, since it is difficult to be introduced into particles obtained by hydrolyzing / condensing the raw material. Therefore, the average particle diameter of the inorganic fine particles is preferably as small as possible, preferably 0.1 μm or less, more preferably 30 nm or less, and still more preferably 10 nm or less. Examples of the inorganic fine particles include silica having an average particle diameter of preferably 0.1 μm or less, more preferably an average particle diameter of 30 nm or less, or even more preferably an average particle diameter of 10 nm or less.
As these inorganic fine particles, a sol dispersed in water or an organic solvent is preferable in that the aggregation of fine particles is small. More preferably, the average particle diameter is 30 nm or less, and still more preferably, it is 1 nm or less.
It is a sol of inorganic fine particles of 0 nm or less. As a specific example, for example, as a sol (silica sol) of silica particles having an average particle diameter of 30 nm or less, trade names "Snowtex 20", "Snowtex O", "Snowtex-C", "Snowtex-C" manufactured by Nissan Chemical Industries, Ltd. Tex-N "," Snowtex-S "," Snowtex-20L "," Snowtex-XS "," Snowtex-XL ",
"Snowtex-YL", "Snowtex-Z"
L "," methanol silica sol "," IPA-ST "and the like. As the alumina sol, trade names" Alumina Sol-100 "and" Alumina Sol-2 "manufactured by Nissan Chemical Industries, Ltd.
00 "," alumina sol-520 "and the like.

During and / or after the condensation step, the radically polymerizable group undergoes a radical polymerization reaction. That is, an intermediate product / particle obtained by hydrolysis / condensation of the first silicon compound and, if necessary, the second silicon compound is subjected to radical polymerization. The radical polymerizable group undergoes a radical polymerization reaction to form an organic polymer skeleton. As a method of radical polymerization, a water-soluble or oil-soluble radical polymerization initiator may be added and dissolved in a solvent slurry containing water of particles obtained by hydrolysis and condensation, and the polymerization may be carried out as it is. The particles obtained by decomposition / condensation are isolated from the slurry using a conventionally known method such as filtration, centrifugation, and concentration under reduced pressure, and then dispersed in a solution containing a radical polymerization initiator, such as water or an organic solvent. May be polymerized
It is not limited to these. In particular, a method in which a radical polymerization initiator is allowed to coexist while the above-mentioned raw materials are hydrolyzed and condensed to simultaneously perform radical polymerization is preferable. The reason for this is that the production of the polysiloxane represented by the formula 4 and the production of the organic polymer by polymerization occur in parallel, so that the above-mentioned organic-inorganic composite particles of the present invention have a hardness, which is a characteristic of inorganic substances, and an organic substance. Organic-inorganic composite particles containing the mechanical resilience and fracture strength, which are the characteristics of the polymer, are easily obtained, and the organic-inorganic composite particles exhibit hardness, mechanical resilience and fracture strength effectively. It is.

Here, as the radical polymerization initiator, conventionally known ones can be used and are not particularly limited.
Preferably, it is at least one compound selected from azo compounds, peroxides and the like. The amount of the above-mentioned radical polymerization initiator is not particularly limited, but when used in a large amount, the calorific value increases, and it becomes difficult to control the reaction.On the other hand, in the case of using a small amount, the radical polymerization may not progress.
For example, 0.1 to 5 wt%, preferably 0.3 to 2 wt%, based on the total weight of the first and second silicon compounds.
Range.

The temperature at the time of radical polymerization can be appropriately selected depending on the radical polymerization initiator to be used.
The range is from 0 to 80 ° C. Further, at the time of radical polymerization, a monomer having a radically polymerizable group and a radically polymerizable group may coexist. Examples of the monomer include unsaturated carboxylic acids such as acrylic acid and methacrylic acid; acrylic esters, methacrylic esters,
Unsaturated carboxylic esters such as crotonic esters, itaconic esters, maleic esters, and fumaric esters; acrylamides; methacrylamides; aromatic vinyl compounds such as styrene, α-methylstyrene, and divinylbenzene Vinyl esters such as vinyl acetate; vinyl compounds such as vinyl halide compounds such as vinyl chloride; and at least one of these may be used. Of these, monomers containing two or more radically polymerizable groups, such as divinylbenzene, trimethylolpropane trimethacrylate, and ethylene glycol dimethacrylate, are preferred.

However, when a large amount of monomer is used, the content of the polysiloxane skeleton in the organic-inorganic composite particles is 2%.
If the content is less than 5 wt%, the hardness becomes insufficient, which is not preferable. For this reason, the amount of the monomer is, for example, 0 to 50 w with respect to the total weight of the first and second silicon compounds.
t%, preferably 0 to 30 wt%. After the radical polymerization, it is better to perform the following recondensation step.
It is preferable because the breaking strength is improved. The recondensation step is a step of further condensing polymer particles generated by radical polymerization in an organic solvent. In promoting the condensation, the above-mentioned catalysts may be used. However, preferable catalysts for further promoting the condensation include titanium tetraisopropoxide, titanium tetrabutoxide, diisopropoxy-bis (acetylacetonate) titanate and the like. Organic aluminum compounds such as aluminum triisopropoxide, aluminum trisec-butoxide, aluminum trisacetylacetonate, aluminum isopropoxide-bisacetylacetonate;
Organic zirconium compounds such as zirconium tetrabutoxide and tetrakis (acetylacetonate) zirconium; organic tin compounds such as dibutyltin diacetate, dibutyltin dilaurate, dibutyltin diethylhexanoate, dibutyltin dimaleate; (CH ₃ O) ₂ P ( = O)
OH, (CH ₃ O) P (＝ O) (OH) ₂ , (C ₄ H ₉ O)
₂ P (＝ O) OH, (C ₈ H ₁₇ O) P (＝ O) (OH) ₂
And any one of them may be used alone, or two or more of them may be used in combination. Among them, at least one selected from the group consisting of an organotin compound and an acidic phosphoric acid ester is preferable.

In the recondensation step, the polymer particles preferably do not contain water. The reason for this is that dehydration condensation of silanol groups proceeds more easily. Therefore, in the recondensation step, when the slurry obtained in the polymerization step does not contain water, the slurry can be used as it is, and when the slurry contains water, the polymer particles are filtered, centrifuged, After separation from the slurry using a conventionally known method such as concentration under reduced pressure, it is preferable to carry out the dispersion in an organic solvent. The organic solvent used is, for example, at least one selected from the group consisting of alcohols, ketones, esters, paraffins, ethers, and aromatic hydrocarbons described above. Further, the recondensation step is performed, for example, at 50
The reaction is performed by stirring the organic solvent slurry containing the polymer particles at a temperature of 200 to 200 ° C, preferably 60 to 150 ° C for 30 minutes to 100 hours. The pressure is normal pressure,
Either reduced pressure or increased pressure may be used.

Next, the polymer particles produced by radical polymerization are isolated from the slurry by a conventionally known method such as filtration, centrifugation, and concentration under reduced pressure, and then the temperature is 800 ° C. or less, preferably 100 to 600 ° C. Temperature, more preferably at a temperature of 150 to 500 ° C., the organic-inorganic composite particles of the present invention having appropriate hardness, mechanical resilience and breaking strength by performing a heat treatment for drying and firing. can get. The composite particles have an organic polymer skeleton and
A polysiloxane skeleton having in its molecule organic silicon in which a silicon atom is directly chemically bonded to at least one carbon atom in the organic polymer skeleton. However, in the heat treatment at a low temperature, the following formula 8 present in the siloxane unit represented by the formula 5:

[0069]

Embedded image

The dehydration condensation reaction between silanol groups represented by
If the required hardness cannot be obtained due to insufficient response
There is a case. That is, the 10% compression modulus of the particles is 350
kg / mm ^TwoIt may not be more than this. Also, 800 ° C
Decomposition of organic polymer is remarkable by heat treatment at higher temperature
Required mechanical resilience and fracture strength
That is, the residual displacement after 10% deformation of the particles is 0 to 5
%, And too hard to compress 10% of the particles
3000 kg / mm^TwoBeyond. Further heat treatment
The atmosphere in which the organic polymer is used can be used without any limitation.
To suppress the decomposition of the material and obtain the necessary mechanical resilience
More preferably, the atmosphere is in a vacuum. Heat treatment
When the temperature is in the range of 200 ° C to 800 ° C, the organic matter of the present invention
Atmosphere during heat treatment to obtain inorganic composite particles
Preferably, the oxygen concentration in the solution is 10% by volume or less,
If the heat treatment temperature is 200 ° C or less, the present invention can be used even in air.
Organic-inorganic composite particles are formed.

When preparing the organic-inorganic composite particles, the above-mentioned raw materials, inorganic fine particles, water / catalyst for hydrolytic condensation, monomers, types and / or amounts of radical polymerization initiators, heat treatment temperature / time / atmosphere By appropriately selecting the oxygen concentration, it is possible to obtain organic-inorganic composite particles in which the amount of SiO _{2 in} the polysiloxane skeleton can be arbitrarily controlled at 25 wt% or more and the average particle diameter can be arbitrarily controlled at 0.5 μm or more. . Since the method for producing organic-inorganic composite particles of the present invention includes the above-described condensation step, polymerization step, and heat treatment step, the polysiloxane skeleton and the organic polymer skeleton have a structure in which they are chemically bonded by Si-C bonds, Organic-inorganic composite particles having high hardness, which is a characteristic of the polysiloxane skeleton, and high mechanical resilience and breaking strength, which are the characteristics of the organic polymer skeleton, can be produced. For this reason, the generated composite particles maintain the gap distance between a pair of members to be arranged at an accurate interval with a small amount of mechanical restoration required to maintain the gap distance between the pair of members constant. In addition to having the hardness and the breaking strength necessary to perform these processes, it is difficult to cause physical damage to those members. Moreover, the composite particles obtained by the production method of the present invention have an average particle diameter of 0.5 μm or more, and thus are useful for forming a gap between a pair of members.

During at least one step selected from a condensation step, a polymerization step, a recondensation step and a heat treatment step, and / or
Alternatively, the resulting particles are colored to obtain colored organic-inorganic composite particles. The production method of the present invention can produce colored organic-inorganic composite particles by introducing dyes and / or pigments into particles in the presence of dyes and / or pigments in appropriate steps during production. . Preferably, it is colored by using a dye and / or a pigment in the condensation step in the production method of the present invention. Dyes and dyeing colors include those described above. Among them, basic dyes are preferred. This is because the silanol groups in the polysiloxane are acidic, so that a basic (cationic) dye is easily adsorbed and dyed. Pigments include, for example, carbon black, iron black, chrome vermillion, molybdenum red, red iron, graphite, chrome green, cobalt green, ultramarine,
There are inorganic pigments such as navy blue; organic pigments such as phthalocyanine, azo, and quinacridone. However, a pigment is preferably used because a pigment may not be introduced into the composite particles of the present invention unless its average particle diameter is 0.4 μm or less. The organic-inorganic composite particles of the present invention colored in this way have both the above-described hardness, mechanical resilience, and breaking strength, and are particularly useful for improving the image quality of a liquid crystal display panel. [Conductive particles] The organic-inorganic composite particles of the present invention can be used as conductive particles.

The conductive particles have the organic-inorganic composite particles of the present invention and a conductor layer formed on the surface of the organic-inorganic composite particles. Since the conductive particles have the organic-inorganic composite particles of the present invention, the mechanical recovery required for maintaining a constant gap distance between a pair of electrodes that are electrically connected to each other and the small number of particles It has the hardness and breaking strength necessary to keep the gap distance constant, and hardly causes physical damage to the electrodes. For this reason, it is easy to keep the gap distance between a pair of electrodes constant, the conductive layer is peeled off by pressure, short-circuit between electrodes that should not be electrically connected, and between electrodes that should be electrically connected. Poor contact is prevented.

The metal used for the conductor layer may be a conventionally known metal, such as nickel, gold, silver, copper, indium, or an alloy thereof. In particular, nickel, gold, and indium are conductive It is preferable because of high performance. The thickness of the conductor layer is not particularly limited as long as there is sufficient conduction,
The range of 0.01 to 5 μm is preferable, and 0.02 to 2 μm
Is particularly preferred. If the thickness is smaller than the above range, the conductivity may be insufficient. If the thickness is larger than the above range, the conductor layer is easily peeled off due to the difference in thermal expansion coefficient between the particles and the conductor layer. The conductor layer may be one layer or two or more layers.
When there are more than one layer, layers made of different conductors may be arranged one above the other.

As a method for forming a conductor layer on the surface of the organic-inorganic composite particles of the present invention, a conventionally known method is adopted, and is not particularly limited. (E.g., vacuum deposition, sputtering, and ion plating). Among them, a chemical plating method is preferable because the conductive particles of the present invention can be easily obtained. The conductive particles of the present invention obtained in this way have both the hardness and the mechanical restorability, which are the characteristics of the above-mentioned organic-inorganic composite particles of the present invention. Therefore, it is particularly useful as an electrical connection material for electronics such as a liquid crystal display panel, an LSI, and a printed wiring board. [Spacer for Liquid Crystal Display Panel] The organic-inorganic composite particles of the present invention can be used as a spacer for a liquid crystal display panel.

The spacer for a liquid crystal display panel (the first spacer for a liquid crystal display panel) comprising the organic-inorganic composite particles of the present invention has a constant gap distance between a pair of electrode substrates to be arranged at an accurate interval. It has the mechanical resilience required for holding, the hardness and the breaking strength necessary for holding the gap distance constant with a small number, and hardly causes physical damage to the electrode substrate. For this reason, the gap distance between the pair of electrode substrates is easily maintained constant, the vapor deposition layer, the alignment film, and the coating layer are less likely to be damaged by pressure, and the shrinkage in a low-temperature environment is close to the shrinkage of the liquid crystal. The number of sprays between the substrates is reduced.

As described above, the organic-inorganic composite particles of the present invention contain both a polysiloxane skeleton and an organic polymer skeleton, and are composite particles in which the polysiloxane skeleton and the organic polymer skeleton are chemically bonded. Since these particles have both high hardness, which is a characteristic of inorganic materials, and high mechanical resilience and breaking strength, which are characteristics of organic polymers, they are suitably used as spacers for liquid crystal display panels. The organic-inorganic composite particles of the present invention contain a dye and / or
Alternatively, when the spacer is colored by containing a pigment, the first liquid crystal display panel spacer is useful as a colored spacer.

In a liquid crystal display panel, when a voltage is applied between the electrode substrates, the liquid crystal causes an optical change to form an image. On the other hand, the spacer does not show an optical change by voltage application. Therefore, in a dark portion when an image is displayed, the uncolored spacer may cause light leakage and may be recognized as a bright spot, which may lower the image quality contrast. When the first spacer for a liquid crystal display panel is made of the organic-inorganic composite particles of the present invention which is colored by containing a dye and / or a pigment, the spacer is colored so that light leakage hardly occurs and the image quality is reduced in contrast. This is particularly useful for improving the image quality of a liquid crystal display panel because it has both the hardness, mechanical resilience, and breaking strength, which are the characteristics of the composite particles of the present invention described above. The preferred color of the colored spacer for a liquid crystal display panel is a color that hardly transmits or does not transmit light. For example, black, dark blue, dark blue, purple, blue, dark green,
Green, brown, red and the like, but particularly preferred,
Black, dark blue and dark blue.

Further, the spacer for a liquid crystal display panel (the second spacer for a liquid crystal display panel) comprising the organic-inorganic composite particles of the present invention and an adhesive layer formed on the surface of the organic-inorganic composite particles has an adhesive property. Useful as a spacer.
The adhesive layer exhibits adhesiveness when heated, for example. The second liquid crystal display panel spacer is interposed between the electrode substrates constituting the liquid crystal display panel and is heated and pressed, so that the adhesive layer is melted and adheres to the electrode substrate, and the adhesive layer is cooled. It is fixed by solidification. For this reason, the second liquid crystal display panel spacer does not easily move in the gap between the electrode substrates, so that the alignment film can be prevented from being damaged, the gap distance can be kept uniform, and the image quality can be improved. As the adhesive layer, a thermoplastic resin is preferable. The glass transition temperature of the thermoplastic resin is preferably 150 ° C. or lower, more preferably 80 ° C. or lower. This is because the substrate adheres to the substrate by heating and pressing for a short time. If the glass transition temperature is too high,
In some cases, the adhesive does not adhere to the substrate even when heated. On the contrary, if the temperature is too low, the spacers are easily fused to each other. The type of the thermoplastic resin is not particularly limited, but is preferably a (meth) acrylic resin. The adhesive layer may be one layer or two or more layers, and in the case of two or more layers, layers made of different thermoplastic resins may be arranged one above the other.

The second spacer for a liquid crystal display panel can be obtained, for example, by coating the organic-inorganic composite particles of the present invention with an adhesive layer. When using a thermoplastic resin as the adhesive, specifically, in situ polymerization method, core cervation method, interfacial polymerization method, liquid curing coating method,
The surface of the organic-inorganic composite particles of the present invention is coated with a thermoplastic resin layer by a conventionally known resin coating method such as a liquid drying method, a high-speed airflow impact method, an air suspension coating method, and a spray drying method. The high-velocity air impact method is preferable because it can be easily coated. The high-velocity air impact method is, for example, mixing the organic-inorganic composite particles of the present invention with a thermoplastic resin powder, dispersing the mixture in the gas phase, and applying mechanical force mainly based on impact force. Is applied to the composite particles and the thermoplastic resin powder to coat the surface of the organic-inorganic composite particles with the thermoplastic resin, which can be easily coated, which is preferable.

Examples of the apparatus utilizing such a high-speed air-flow impact method include a hybridization system manufactured by Nara Machinery Co., Ltd., a mechanofusion system manufactured by Hosokawa Micron Corporation, and a cryptotron system manufactured by Kawasaki Heavy Industries, Ltd. is there. The second liquid crystal display panel spacer is:
The above-mentioned organic-inorganic composite particles of the present invention have both the hardness, mechanical resilience, and breaking strength, which are the characteristics of the organic-inorganic composite particles, and have adhesiveness, so that they are particularly useful for improving the image quality of a liquid crystal display panel. When the organic-inorganic composite particles are colored by including a dye and / or a pigment, the second spacer for a liquid crystal display panel is colored so that light leakage hardly occurs and a decrease in image quality contrast is prevented. It is difficult to move in the gap between the electrode substrates due to having, and it is possible to prevent damage to the alignment film and maintain uniformity of the gap distance,
Since it has both hardness, mechanical resilience, and breaking strength, which are the characteristics of the composite particles of the present invention described above, it is an adhesive spacer that is also useful as a colored spacer, and in order to improve the image quality of a liquid crystal display panel. Particularly useful. (Liquid crystal display panel) In a conventional liquid crystal display panel, instead of the conventional spacer, a liquid crystal display panel in which a spacer for a liquid crystal display panel comprising the organic-inorganic composite particles of the present invention as described above is interposed between electrode substrates is Have the same or substantially the same gap distance as the particle size of the spacer. The amount of the spacer used is usually 40 to 100 / mm ² , preferably 40 to 80 / mm ² , which is about 10 to 50% smaller than that of the conventional organic particle spacer, and does not form an image. The area of the portion is reduced, and the amount of impurities such as ions and molecules eluted from inside the spacer into the liquid crystal layer is also reduced. This results in higher contrast,
Roughness is reduced and display quality is expected to improve.

Such a liquid crystal display panel is, for example, a first liquid crystal display panel.
An electrode substrate, a second electrode substrate, a spacer for a liquid crystal display panel, a sealing material, and a liquid crystal are provided. The first electrode substrate has a first substrate and a first electrode formed on a surface of the first substrate. The second electrode substrate has a second substrate and a second electrode formed on the surface of the second substrate, and faces the first electrode substrate. The liquid crystal display panel spacer is interposed between the first electrode substrate and the second electrode substrate. The sealant adheres the first electrode substrate and the second electrode substrate at a peripheral portion. The liquid crystal is the first
The space surrounded by the electrode substrate, the second electrode substrate, and the sealing material is filled. For such a liquid crystal display panel, those other than the spacer, such as an electrode substrate, a sealing material, and a liquid crystal, can be used in the same manner as the conventional one in the same manner.
The electrode substrate is a substrate such as a glass substrate or a film substrate,
And an alignment film formed on the surface of the electrode substrate as necessary to cover the electrodes. As the sealing material, an epoxy resin adhesive sealing material or the like is used. As the liquid crystal, those conventionally used may be used, for example, biphenyl, phenylcyclohexane, Schiff base, azo, azoxy, benzoate, terphenyl, cyclohexylcarboxylate, biphenylcyclohexane , Pyrimidine, dioxane, cyclohexylcyclohexane ester, cyclohexylethane, cyclohexene, and fluorine liquid crystals can be used.

As a method of manufacturing such a liquid crystal display panel, for example, a spacer comprising the organic-inorganic composite particles of the present invention is used as an in-plane spacer and a wet method or a wet method is applied to one of the two electrode substrates. A spacer made of the organic-inorganic composite particles of the present invention is dispersed uniformly in an adhesive sealing material such as an epoxy resin as a sealing spacer, and then is screened on the adhesive sealing portion of the other electrode substrate. Place what is applied by means such as printing, apply moderate pressure, 100 ~
After heating and curing the adhesive sealing material by heating at a temperature of 180 ° C. for 1 to 60 minutes, or by irradiating an ultraviolet ray with an irradiation amount of 40 to 300 mJ / cm ² , a liquid crystal is injected, and the injection portion is sealed. There can be mentioned a method of obtaining a liquid crystal display panel,
The present invention is not limited by the method for manufacturing the liquid crystal display panel. As the in-plane spacer, among the spacers for a liquid crystal display panel comprising the organic-inorganic composite particles of the present invention, the colored first spacer for a liquid crystal display panel is preferable because light leakage hardly occurs. The spacer for the display panel is more preferable because it is fixed to the substrate and is less likely to move, and the colored spacer for the second liquid crystal display panel is more preferable because it is less likely to cause light leakage and is harder to move because it is fixed to the substrate.

Such a liquid crystal display panel is used for the same purpose as a conventional liquid crystal display panel, for example, as an image display element of a television, a personal computer, a word processor or the like.

[0085]

EXAMPLES Examples of the present invention and comparative examples outside the scope of the present invention will be shown below, but the present invention is not limited to the following examples. The liquid crystal display panel in the following examples was manufactured by the following method. As shown in FIG. 1, first, 300 mm × 34
After forming an electrode (for example, a transparent electrode) 5 and a polyimide alignment film 4 on a lower glass substrate 11 of 5 mm × 1.1 mm, rubbing was performed to obtain a lower electrode substrate 110. On the lower electrode substrate 110, a spacer for a liquid crystal display panel comprising the organic-inorganic composite particles of the present invention in a mixed solvent of 30 parts by volume of methanol, 20 parts by volume of isopropanol, and 50 parts by volume of water (in this case, an in-plane spacer) 8 was uniformly dispersed so as to be 1% by weight, and sprayed for 1 to 10 seconds.

On the other hand, electrodes (for example, transparent electrodes) 5 are placed on upper glass substrate 12 of 300 mm × 345 mm × 1.1 mm.
After forming the polyimide alignment film 4, rubbing was performed to obtain the upper electrode substrate 120. Then, a liquid crystal display panel spacer (in this case, a seal spacer) 3 composed of the organic-inorganic composite particles of the present invention dispersed in the epoxy resin adhesive sealing material 2 so as to have a volume ratio of 30% by volume is formed on the upper electrode. Screen printing was performed on the adhesive seal portion of the substrate 120. Finally, the upper and lower electrode substrates 120 and 110 are
The electrodes 5 and the alignment film 4 are bonded to each other via a spacer 8 made of the organic-inorganic composite particles of the present invention so as to face each other, a pressure of 4 kg / cm ² is applied, and the mixture is heated at 150 ° C. for 30 minutes. The adhesive sealing material 2 was cured by heating. Thereafter, the gap between the two electrode substrates 120 and 110 is evacuated and then returned to the atmospheric pressure, whereby the liquid crystal 7 mixed with a liquid crystal material such as biphenyl or phenylcyclohexane depending on the type of liquid crystal display panel to be manufactured. Was injected, and the injection part was sealed. Then, the upper and lower glass substrates 12,
A PVA (polyvinyl alcohol) -based polarizing film 6 was attached to the outside of 11 to obtain a liquid crystal display panel.

As shown in FIG. 2, the spacer 8 may be made of uncolored organic-inorganic composite particles 31 of the present invention. At this time, physical damage to the electrode substrate due to pressing during manufacture hardly occurs, and low-temperature foaming and image unevenness hardly occur. In addition, since the number of spacers can be reduced as compared with a conventional spacer made of polymer particles, the area of a portion where no image is formed is reduced, and the amount of impurities eluted into the liquid crystal is also reduced. For this reason,
Display quality such as contrast can be improved. As shown in FIG. 3, the spacers 8 may be made of colored organic-inorganic composite particles 32 of the present invention. At this time, since light leakage due to the spacer 8 is less likely to occur, the advantage that the bright spot becomes less conspicuous and the display quality is further improved is obtained.

As shown in FIG. 4, the spacer 8 may include the organic-inorganic composite particles 31 of the present invention which are not colored and the adhesive layer 33 formed on the surface of the particles 31. At this time, since the spacers are less likely to move, damage to the alignment film is prevented, and the advantage of further improving display quality is further obtained. As shown in FIG. 5, the spacer 8 may include colored organic-inorganic composite particles 32 of the present invention and an adhesive layer 33 formed on the surface of the particles 32. At this time, light leakage due to the spacer 8 is less likely to occur, so that bright spots are less noticeable and display quality is further improved. Further, since the spacer is less likely to move, damage to the alignment film is prevented, and display quality is reduced. The advantage of further enhancement is further obtained.

As shown in FIG. 6, the conductive particles include the organic-inorganic composite particles 34 of the present invention and a conductive layer 35 formed on the surface of the particles 34. The conductor layer 35 is, for example, a metal film formed by electroless plating.
It may be a layer or two or more layers. Regarding the evaluation method of the obtained liquid crystal display panel, low-temperature foaming was performed at −45 ° C. at 10 ° C.
The presence or absence of image display after holding for 00 hours, and the presence or absence of image unevenness and pixel defects at room temperature (25 ° C.) were visually observed. Example 1 A solution obtained by mixing 2.9 g of a 25% aqueous ammonia solution, 10.1 g of methanol, and 141.1 g of water in a four-necked flask equipped with a cooling pipe, a thermometer, and a dropping port (solution A).
And kept at 25 ± 2 ° C., and while stirring, γ-methacryloxypropyltrimethoxysilane 2
A solution (solution B) obtained by mixing 7 g, methanol 54 g, and 0.14 g of 2,2'-azobis- (2.4-dimethylvaleronitrile) as a radical polymerization initiator was added from a dropping port, and γ-methacryloxypropyl was added. Hydrolysis and condensation of trimethoxysilane were performed. 20 with continuous stirring
After minutes, the mixture was heated to 70 ± 5 ° C. in an N ₂ atmosphere to perform radical polymerization.

After continuing heating for 2 hours, the mixture is cooled to room temperature,
A suspension of polymer particles was obtained. This suspension was subjected to solid-liquid separation by filtration, and the obtained cake was washed with methanol for 3 hours.
This was repeated twice, and the obtained polymer particles were vacuum-dried in a vacuum dryer at 200 ° C. for 2 hours to obtain composite particles (1). The obtained composite particles (1) had an average particle size of 4.24.
μm, coefficient of variation 3.8%, amount of SiO ₂ constituting the polysiloxane skeleton 34.7 wt%, 10% compression modulus 48
It was 0 kg / mm ² , the residual displacement after 10% deformation was 2.2%, and the breaking strength was 2.4 g. Regarding the composite particles (1),
By FT-IR analysis, the organic polymer skeleton —CH ₂ —
Spectrum assigned to CH _2- (650-800 c
m ^-1 ) and a spectrum (11) assigned to -Si-CH _2-.
50 to 1300 cm ^-1 ).

From these results, the composite particles (1) were:
It can be seen that the organic-inorganic composite particles include an organic polymer skeleton and a polysiloxane skeleton having in its molecule an organic silicon in which a silicon atom is directly chemically bonded to at least one carbon atom in the organic polymer skeleton. Using this composite particle (1), a B-size STN type liquid crystal display panel was produced by a known method. As a result, the number of sprayed particles can be reduced by 10% or more with respect to the existing organic particle spacer (Epostor GP-H manufactured by Nippon Shokubai Co., Ltd.). Neither low-temperature bubbling nor image unevenness occurred when using.

Example 2 In Example 1, the composition of Solution B was changed to γ-methacryloxypropyltrimethoxysilane 1
9.2 g, methanol 51 g, 2,2'-azobis-
(2,4-dimethylvaleronitrile) 0.10 g, tetraethoxysilane dimer to pentamer (“silicate 40” manufactured by Tama Chemical Co., Ltd., 40 wt% as SiO ₂ ) 4.2
The procedure of Example 1 was repeated, except that g was changed to g, to obtain composite particles (2). The obtained composite particles (2)
Average particle diameter 2.02 μm, coefficient of variation 7.4%, amount of SiO ₂ constituting polysiloxane skeleton 42.7 wt%, 1
The 0% compression modulus was 720 kg / mm ² , the residual displacement after 10% deformation was 3.6%, and the breaking strength was 1.0 g. About composite particle (2), in the same manner as in Example 1, -CH _2-
Spectrum assigned to CH _2- (650-800 c
m ^-1 ) and a spectrum (11) assigned to -Si-CH _2-.
50 to 1300 cm ^-1 ).

Using the composite particles (2), a B5 size large ferroelectric liquid crystal display panel was produced by a known method, and the same results as in Example 1 were obtained. Example 3 In Example 1, the composition of Solution B was changed to 40.5 g of γ-methacryloxypropyltrimethoxysilane, 50.6 g of methanol, and 2,2′-azobis- (4-methoxy-2,4-dimethylvalero). Nitrile) 0.20 g,
The solution was changed to 4.5 g of divinylbenzene, the solution A was kept at 50 ± 5 ° C., and the solution B was added dropwise over 20 minutes while stirring in an N ₂ atmosphere, and radical polymerization was carried out while hydrolyzing and condensing. The procedure of Example 1 was repeated to obtain a composite particle (3).

The obtained composite particles (3) had an average particle size of 8.91 μm, a coefficient of variation of 4.8%, an amount of SiO ₂ constituting the polysiloxane skeleton of 29.5 wt%, and a 10% compression modulus of 370 kg /. mm ² , residual displacement after 10% deformation 2.
The breaking strength was 8% and the breaking strength was 9.7 g. For composite particles (3), in the same manner as in Example 1, -CH ₂ -CH ₂ - spectra attributed to the (650~800cm ^-1) -Si-
Spectrum assigned to CH ₂ — (1150 to 1300 c
m ^-1 ). Using this composite particle (3), a B5-size TN type liquid crystal display panel was produced by a known method, and the same results as in Example 1 were obtained.

Example 4 The procedure of Example 1 was repeated, except that vinyltrimethoxysilane was used instead of γ-methacryloxypropyltrimethoxysilane. The resultant was vacuum-dried at 200 ° C. for 2 hours and then at 600 ° C. for 2 hours in an N ₂ atmosphere. The procedure of Example 1 was repeated, except for firing, to obtain composite particles (4). The obtained composite particles (4) had an average particle size of 4.18 μm, a coefficient of variation of 7.2%, an amount of SiO ₂ constituting the polysiloxane skeleton of 40.9 wt%, a 10% compression modulus of 1050 kg / mm ² , The residual displacement after 10% deformation was 3.2%, and the breaking strength was 1.9 g. For composite particles (4), in the same manner as in Example 1, -CH ₂ -C
Spectrum assigned to H _2- (650 to 800 cm ^-1 )
And the spectrum assigned to —Si—CH ₂ — (1150
１1300 cm ⁻¹ ).

Using this composite particle (4), a B5 size large STN type liquid crystal display panel was produced by a known method, and the same results as in Example 1 were obtained. [Example 5] In Example 1, the solution A was mixed with silica sol ("Snowtex-XS" SiO2 ₂ manufactured by Nissan Chemical Industries, Ltd.).
The procedure of Example 1 was repeated, except that 15 g of 0 wt% (particle size: 4 to 6 nm) was added, to obtain composite particles (5). The obtained composite particles (5) had an average particle size of 4.77.
μm, coefficient of variation 4.0%, amount of SiO ₂ constituting the polysiloxane skeleton 42.0 wt%, 10% compression modulus 11
30 kg / mm ² , 2.5% residual displacement after 10% deformation,
The breaking strength was 3.8 g. For composite particles (5), in the same manner as in Example 1, -CH ₂ -CH ₂ - spectra attributed to (650～800Cm ^-1) and -Si-CH
₂ - spectra attributed to (1150～1300C
m ^-1 ).

Using this composite particle (5), a TFT type liquid crystal display panel of B5 size was produced by a known method, and the same result as in Example 1 was obtained. Examples 6 to 9 Example 5 was repeated except that the type and amount of the silica sol were changed as shown in Table 1.
Were repeated to obtain composite particles (6) to (9). The average particle diameter, variation coefficient, and SiO ₂ constituting the polysiloxane skeleton of the obtained composite particles (6) to (9)
Table 1 shows the amount of, 10% compression modulus, 10% residual displacement after deformation, and breaking strength. Regarding the composite particles (6) to (9), in the same manner as in Example 1, the spectrum (650 to 800 cm ⁻¹ ) attributed to —CH ₂ —CH ₂ — and —Si—C
Spectrum assigned to H _2- (1150 to 1300 cm
^-1 ).

A B5-size large STN-type liquid crystal display panel was produced using the composite particles (6) to (9) by a known method, and the same results as in Example 1 were obtained. Example 10 The composite particles (8) obtained in Example 8 were further heat-treated at 400 ° C. for 2 hours in a mixed gas of 95% by volume of nitrogen and 5% by volume of oxygen to obtain composite particles (10). Was. The average particle diameter, the coefficient of variation, the amount of SiO ₂ constituting the polysiloxane skeleton of the obtained composite particles (10),
Table 1 shows the 10% compression modulus, the residual displacement after 10% deformation, and the breaking strength. Regarding the composite particles (10), in the same manner as in Example 1, the spectrum (650 to 800 cm ⁻¹ ) belonging to —CH ₂ —CH ₂ — and the spectrum (1150 to 800) belonging to —Si—CH ₂ — 1300 cm ^-1 ).

A B5-size large STN type liquid crystal display panel was produced by a known method using the composite particles (10).
In each case, the same results as in Example 1 were obtained.

[0100]

[Table 1]

Example 11 The acid dye Kayac
yl Sky Blue R (manufactured by Nippon Kayaku Co., Ltd.) 5
g of water in 100 g of water and a dispersion of 10 g of the composite particles (8) obtained in Example 8 in 500 g of water were mixed and heated under pressure at 150 ° C. for 1 hour in an autoclave. . After the treatment, the deep blue colored particles were collected by filtration, washed three times with water, and then dried in vacuum at 200 ° C. to obtain deep blue colored composite particles (11). The obtained composite particles (11) had an average particle diameter of 4.2.
6 μm, coefficient of variation 6.3%, amount of SiO ₂ constituting polysiloxane skeleton 40.0 wt%, 10% compression modulus 9
20 kg / mm ² , 3.0% residual displacement after 10% deformation,
The breaking strength was 3.0 g. For composite particles (11), in the same manner as in Example 1, -CH ₂ -CH ₂ - spectra attributed to (650～800Cm ^-1) and -Si-CH
₂ - spectra attributed to (1150～1300C
m ^-1 ).

A B5-size large STN-type liquid crystal display panel was produced using the composite particles (11) by a known method. The same results as in Example 8 were obtained, and a bright spot (light leakage) was observed. There were few. [Example 12] Kayacryl B which is a basic dye
Lack NP200 (manufactured by Nippon Kayaku Co., Ltd.) (5 g) was dissolved in water (300 g), acetic acid was added to adjust the pH to 4, 10 g of the composite particles (8) obtained in Example 8 was added, and the mixture was stirred at 95 ° C. with good stirring. For 8 hours to obtain composite particles (12) colored black.

The obtained composite particles (12) had an average particle diameter of 4.41 μm, a coefficient of variation of 5.7%, an amount of SiO ₂ constituting the polysiloxane skeleton of 40.2 wt%, and a 10% compression modulus of 920 kg /. mm ² , the residual displacement after 10% deformation was 2.8%, and the breaking strength was 3.4 g. Composite particles (1
For 2), in the same manner as in Example 1, -CH ₂ -CH ₂
Spectrum (650-800 cm ^-1 ) belonging to-
Spectra assigned to Si—CH ₂ — (1150 to 1
300 cm ^-1 ). Using this composite particle (12), a B5 size STN type liquid crystal display panel was produced by a known method, and the same results as in Example 11 were obtained.

Example 13 The procedure of Example 8 was repeated except that the basic dye Kayacryl Black NP2 was added to Solution A.
The procedure of Example 8 was repeated except that 1 g of 00 (manufactured by Nippon Kayaku Co., Ltd.) was added to obtain composite particles (13) colored black. The obtained composite particles (13) had an average particle diameter of 4.53 μm, a coefficient of variation of 5.1%, and the amount of SiO ₂ constituting the polysiloxane skeleton was 40.4 wt% and 10%.
The compression modulus was 970 kg / mm ² , the residual displacement after 10% deformation was 2.5%, and the breaking strength was 3.6 g. About composite particle (13), in the same manner as in Example 1, -CH _2-
Spectrum assigned to CH _2- (650-800 c
m ^-1 ) and a spectrum (11) assigned to -Si-CH _2-.
50 to 1300 cm ^-1 ).

Using this composite particle (13), a B5 size large STN type liquid crystal display panel was produced by a known method, and the same results as in Example 11 were obtained. [Example 14] Composite particles (8) 3 obtained in Example 8
0g and thermoplastic resin particles (methyl methacrylate 84w
Copolymer of t% and n-butyl acrylate 16 wt%, glass transition temperature 70 ° C, average particle diameter 0.3 μm) 2
g), and the surface of the composite particle (8) is coated with a thermoplastic resin using a hybridization system NHS-O manufactured by Nara Machinery Co., Ltd., and the composite particle (14) having an adhesive layer on the surface. I got Observation of the obtained composite particles (14) having an adhesive layer by SEM showed that
The surface of the composite particle (8) was completely covered with the thermoplastic resin, and the cross section thereof was observed with a TEM. As a result, the thickness of the coating layer was 0.2 μm.

Using the composite particles (14) having the adhesive layer, a B5-size large STN type liquid crystal display panel was produced by a known method, and the same results as in Example 1 were obtained.
Further, when the obtained liquid crystal display plate was similarly displayed before and after being vibrated using a vibrator, no change was observed. [Example 15] In Example 14, the composite particles (8)
The procedure of Example 14 was repeated except that the composite particles (13) colored in black obtained in Example 13 were used instead of the composite particles colored in black having an adhesive layer on the surface. (15) was obtained. Observation of the obtained black-colored composite particles (15) having an adhesive layer by SEM revealed that the surface of the composite particles (13) was completely covered with a thermoplastic resin, and the cross-section of the composite particles (13) was TEM. As a result, the thickness of the coating layer was 0.2 μm.

Using the black-colored composite particles (15) having the adhesive layer, a B5-sized S
When a TN type liquid crystal display panel was produced, the same results as in Example 14 were obtained. Example 16 The composite particles (8) obtained in Example 8 were subjected to electroless Ni plating to obtain conductive particles (16).
The obtained conductive particles (16) had an average particle size of 4.92 μm.
m, and the coefficient of variation was 5.4%. When the obtained conductive particles (16) were observed with SEM and XMA, the surface of the conductive particles (16) was completely plated with Ni, and when the cross section was observed with TEM, the thickness of the coating layer was found. Was 0.3 μm.

Example 17 The composite particles (8) obtained in Example 8 were subjected to electroless Ni plating, and further subjected to electroless gold plating to obtain conductive particles (17). The obtained conductive particles (17) had an average particle size of 5.05 μm and a coefficient of variation of 5.5%. Observation of the obtained conductive particles (17) with SEM and XMA revealed that the conductive particles (17)
Was completely plated with Ni, and further plated with Au. When the cross section was observed with a TEM, the thickness of the coating layer was 0.5 μm. Example 18 A suspension of the polymer particles (1) obtained in Example 1 was subjected to solid-liquid separation by decantation, and the obtained cake was dried at room temperature overnight. 5 g was collected from the dried product, ultrasonically dispersed in 200 g of isopropyl alcohol, and 0.5 g of dibutyltin dilaurate was added to the dispersion.
g was added and heated at 80 ° C. for 2 hours with stirring. Thus, a suspension of the recondensed particles (18) was obtained.
Solid-liquid separation, washing and drying were performed in the same manner as in the above to obtain composite particles (18).

The obtained composite particles (18) had an average particle diameter of 4.20 μm, a coefficient of variation of 3.9%, an amount of SiO ₂ constituting the polysiloxane skeleton of 35.1 wt%, and a 10% compression modulus of 950 kg /. mm ² , the residual displacement after 10% deformation was 1.8%, and the breaking strength was 3.0 g. Composite particles (1
For 8), in the same manner as in Example 1, -CH ₂ -CH ₂
Spectrum (650-800 cm ^-1 ) belonging to-
Spectra assigned to Si—CH ₂ — (1150 to 1
300 cm ^-1 ). Using this composite particle (18), a B5-size large STN-type liquid crystal display panel was produced by a known method, and the same results as in Example 1 were obtained.

Example 19 A solution prepared by mixing 1.8 g of a 25% aqueous ammonia solution and 154.8 g of water in a N ₂ atmosphere was placed in a four-necked flask equipped with a cooling tube, a thermometer, and a dropping port. Keep at ± 2 ° C and stir into the solution,
29 g of p-trimethoxysilylstyrene, methanol 7
0 g, 2,2'-azobis (4-methoxy-2,4-dimethylvaleronitrile) as a radical polymerization initiator
A solution containing 0.12 g was added through a dropping port, and p-
Hydrolysis and condensation of trimethoxysilylstyrene were performed. 7 minutes later while continuing the stirring, 55 ± in an N ₂ atmosphere
The mixture was heated to 5 ° C. to perform radical polymerization.

After heating for 15 minutes, the mixture was cooled to room temperature,
A suspension of polymer particles was obtained. This suspension was subjected to solid-liquid separation by filtration, and the obtained cake was washed with methanol for 3 hours.
The process was repeated twice, and the obtained polymer particles were heated at 350 ° C. for 2 hours in an N ₂ atmosphere to obtain composite particles (19). The obtained composite particles (19) had an average particle size of 2.6.
0 μm, coefficient of variation 6.9%, amount of SiO ₂ constituting polysiloxane skeleton 36.7 wt%, 10% compression modulus 7
45 kg / mm ² , 1.8% residual displacement after 10% deformation,
The breaking strength was 1.2 g. Regarding the composite particles (19), in the same manner as in Example 1, the organic polymer skeleton —CH
₂ -CH ₂ - spectra attributed to (650～800Cm
^-1) -Si-C ₆ H ₄ - spectra attributed to the (14
00 to 1450 cm ^-1 and 700 to 710 cm ^-1 ).

From these results, it was found that the composite particles (19)
Indicates that the organic-inorganic composite particles include an organic polymer skeleton and a polysiloxane skeleton having in its molecule an organic silicon in which a silicon atom is chemically bonded directly to at least one carbon atom in the organic polymer skeleton. Using this composite particle (19), a B5 size ferroelectric liquid crystal display panel was produced by a known method, and the same results as in Example 1 were obtained. [Example 20] Raven 1255 which is carbon black
Γ-glycidoxypropyltrimethoxysilane (500 g)
, And the operation of Example 1 was repeated except that 13 g of the mixture kneaded three times at 80 to 90 ° C. with a hot roll was used as the liquid B in the liquid B in Example 1. Composite particles (20) colored black were obtained.

The obtained composite particles (20) had an average particle diameter of 3.92 μm, a coefficient of variation of 3.2%, an amount of SiO ₂ constituting the polysiloxane skeleton of 27.8 wt%, and a 10% compression modulus of 837 kg /. mm ² , the residual displacement after 10% deformation was 2.3%, and the breaking strength was 2.5 g. Composite particles (2
0), in the same manner as in Example 1, the spectrum (650) assigned to —CH ₂ —CH ₂ — in the organic polymer skeleton.
８００800 cm ⁻¹ ) and a spectrum (1150 to 1300 cm ⁻¹ ) attributed to —Si—CH ₂ —. From these results, the composite particles (20) include an organic polymer skeleton and a polysiloxane skeleton having in its molecule an organic silicon in which a silicon atom is chemically bonded directly to at least one carbon atom in the organic polymer skeleton. It can be seen that the particles are organic-inorganic composite particles.

Using the composite particles (20), a B5-size large TFT type liquid crystal display panel was produced by a known method, and the same results as in Example 1 were obtained. Comparative Example 1 The composite particles (1) obtained in Example 1 were further heat-treated at 950 ° C. for 2 hours to obtain particles. The amount of SiO ₂ constituting the polysiloxane skeleton of the particles was 99.8.
wt.%, and from the results of FT-IR analysis, it was found that the silica particles had the organic polymer skeleton decomposed and burned. The 10% compression modulus of the obtained particles is 3250.
kg / mm ² , the residual displacement after 10% deformation was 6.2%. Using these particles, a B5-sized T
When an FT type liquid crystal display panel was manufactured, TF on the electrode substrate was
A pixel defect occurred due to the disconnection of T, and image unevenness occurred due to insufficient mechanical restorability of the particles.

The number of the spacers of the present invention scattered in the plane of the liquid crystal display panel obtained in the above embodiment is such that
The number of spacers of the present invention within an arbitrary 1 mm ² in each of the nine areas divided into three equal parts in the horizontal direction was counted by an optical microscope, and the average value of the total number of nine areas was obtained.
The number of sprays was used. The results were as follows. Example 1 ... number of sprayed pieces 73 / mm ² Example 10 ... number of sprayed pieces 63 / mm ² Example 2 ... number of sprayed pieces 70 / mm ² Example 11 ... number of sprayed pieces 70 / mm ² Example 3 ... number of sprayed pieces 69 / mm ² Example 12: 69 / mm ² sprayed Example 4 68 / mm ² sprayed Example 13 71 / mm ² sprayed Example 5 69 / mm ² sprayed Example 14: Number of scattered pieces 69 / mm ² Example 6 ... Number of scattered pieces 66 / mm ² Example 15 ... Number of scattered pieces 70 / mm ² Example 7 ... Number of scattered pieces 64 / mm ² Example 18: Number of scattered pieces 65 pieces / mm ² example 8: sprayed number 68 / mm ² example 19: scatter number 75 / mm ² example 9 ... sprayed number 52 pieces / mm ² example 20: scatter number 63 / mm ² Comparative Example 2 Using the existing organic particle spacers described in Example 1, a B5 size large STN type liquid crystal display panel was produced by a known method. The liquid crystal panel was unusable as a liquid crystal display panel. At this time, the number of scattered spacers was 66 pieces / mm ² according to the counting method as described above.

Comparative Example 3 In a 2 liter glass reactor equipped with a stirrer, a dropping port and a thermometer, 307 parts by weight of methanol, 6 parts by weight of 25% aqueous ammonia, and 122 parts of water
5 parts by weight were uniformly mixed. This mixture was added to 20 ± 0.5
While adjusting the temperature to 100 ° C and stirring uniformly at 100 rpm, 60 parts by weight of methyltrimethoxysilane was dropped from the dropping port over 6 hours. After the dropwise addition, the mixture was continuously stirred for 1 hour to carry out hydrolysis and condensation to obtain a suspension of fine particles of hydrated condensate of methyltrimethoxysilane. This suspension was subjected to solid-liquid separation by filtration, and the obtained cake was washed with methanol for 3 hours.
The obtained solid content powder was dried in a vacuum dryer at 200 ° C. for 3 hours to obtain an average particle size of 2.04 μm.
m, an organic-inorganic composite particle having a variation coefficient of 7.6% was obtained.
The 10% compression modulus of the obtained composite particles is 370 kg / mm.
² , The residual displacement after 10% deformation was 2.7%, and the breaking strength was 0.2 g. Using the composite particles as a spacer for a liquid crystal display panel, a B5 size large ferroelectric liquid crystal display panel was produced by a known method. However, the composite particles were broken, and image unevenness was remarkably exhibited. It was unusable as a display panel. At this time, the number of the applied spacers was 95 / mm ² according to the counting method described above.

[0117]

The organic-inorganic composite particles of the present invention have a
At least one of organic polymer skeleton and organic polymer skeleton
Organic silicon in which silicon atoms are chemically bonded directly to carbon atoms
A polysiloxane skeleton having in the molecule a
SiO constituting the loxane skeleton _TwoOf 25 wt% or more
Having an average particle size of 0.5 μm or more,
It must be placed at precise intervals because it has additional breaking strength.
Required to maintain a constant gap distance between a pair of members
The gap distance is kept constant with excellent mechanical resilience and a small number.
Having the necessary hardness and breaking strength to carry
In addition, the above-mentioned member of the organic-inorganic composite particles of the present invention
The production method includes a radical polymerizable group capable of hydrolysis and condensation.
Condensation by hydrolysis and condensation using the first silicon compound
Step and during and / or after the condensation step
A polymerization step of subjecting a cal-polymerizable group to a radical polymerization reaction,
At a temperature of 800 ℃ or less, the polymer particles produced in the combining step,
Heat treatment at a temperature of preferably 100 ° C to 600 ° C
Process, so that the organic polymer skeleton and its
The polysiloxane skeleton bonded to the inside and the surface of the particle
1 that should be evenly distributed and accurately spaced
Machine required to maintain a constant gap distance between a pair of members
Keeps the gap distance constant with mechanical resilience and a small number
With the necessary hardness and breaking strength to
In addition, an organic material that does not easily cause physical damage to the member
The porous inorganic composite particles can be easily produced.

[Brief description of the drawings]

FIG. 1 is a partial cross-sectional view showing one embodiment of a liquid crystal display panel using the organic-inorganic composite particles of the present invention.

FIG. 2 is a cross-sectional view illustrating one embodiment of a spacer for a liquid crystal display panel comprising organic-inorganic composite particles of the present invention.

FIG. 3 is a cross-sectional view showing one embodiment of a spacer for a liquid crystal display panel comprising organic-inorganic composite particles of the present invention.

FIG. 4 is a cross-sectional view showing one embodiment of a spacer for a liquid crystal display panel comprising organic-inorganic composite particles of the present invention.

FIG. 5 is a cross-sectional view illustrating one embodiment of a spacer for a liquid crystal display panel comprising organic-inorganic composite particles of the present invention.

FIG. 6 is a cross-sectional view illustrating one embodiment of the conductive particles of the present invention.

[Explanation of symbols]

 DESCRIPTION OF SYMBOLS 2 Adhesive sealing material 3 Seal part spacer 4 Alignment film 5 Electrode 6 Polarization film 7 Liquid crystal 8 In-plane spacer 11 Lower glass substrate 12 Upper glass substrate 31 Organic-inorganic composite particles 32 Organic-inorganic composite particles 33 Adhesive layer 34 Organic-inorganic Composite particle 35 Conductive layer 110 Lower electrode substrate 120 Upper electrode substrate

Claims (10)

[Claims] 1. An organic polymer skeleton comprising: an organic polymer skeleton; and a polysiloxane skeleton having in its molecule an organic silicon in which a silicon atom is chemically bonded directly to at least one carbon atom in the organic polymer skeleton. Si
The amount of O ₂ is at least 25 wt%, has an average particle size of at least 0.5 μm, and has the following formula: (Where G indicates breaking strength [kg]; Y indicates particle diameter [m
m]), the organic-inorganic composite particles further having a fracture strength. 2. The organic-inorganic composite particles according to claim 1, wherein the coefficient of variation of the particle diameter is 20% or less. 3. A 10% compression modulus of 350 to 3000 kg /
The organic-inorganic composite particles according to claim 1 or 2, which have a size of mm ² . 4. The organic-inorganic composite particles according to claim 1, which are colored by containing at least one selected from the group consisting of dyes and pigments. 5. The following general formula 1: (Where R ¹ represents a hydrogen atom or a methyl group;
² represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ³ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, And at least one monovalent group selected from the group consisting of an acyl group) and the following general formula 2: (Where R ⁴ represents a hydrogen atom or a methyl group;
⁵ represents at least one monovalent group selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, and an acyl group having 2 to 5 carbon atoms), and the following general formula 3: Chemical formula 3] (Where R ⁶ represents a hydrogen atom or a methyl group;
⁷ represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ⁸ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, At least one monovalent group selected from the group consisting of acyl groups) and at least one radical polymerization selected from the group consisting of compounds represented by the general formula selected from the group consisting of Using a first silicon compound having a functional group, if necessary, a compound of the general formula 5 (Where X is CH ₂ ＣC (-R ¹ ) -COOR ^2- ,
^{_{CH 2 = C (-R 4)}} - , or ^{_{CH 2 = C (-R 6)}} -R 7
- a monovalent radical-polymerizable functional group represented by; R ¹ and R ⁴ and R ⁶ represents a hydrogen atom or a methyl group; R ² and R ⁷
Represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ⁹ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, R ¹⁰ represents at least one monovalent group selected from the group consisting of an acyl group; R ¹⁰ represents an alkyl group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms, And m represents an integer of 2 to 3; n represents an integer of 0 to 2; m + n represents an integer of 2 to 3; A plurality of Xs may be different from each other, and 2
More than one may be the same. When n is 2, two R
¹⁰ may be different from each other or may be the same. For 4-m-n is 2, the two R ⁹ are may be different from each other, at least one selected from the compounds represented by either the same or) and the group consisting of a derivative thereof, the radical Hydrolysis / condensation using a polymerizable group-containing second silicon compound, and without using a radical polymerizable monomer other than the radical polymerizable group-containing first silicon compound and the radical polymerizable group-containing second silicon compound. A condensation step; a polymerization step of performing a radical polymerization reaction of a radical polymerizable group during and / or after the condensation step;
And an organic-inorganic composite particle obtained by a production method comprising: 6. A compound represented by the following general formula 1: (Where R ¹ represents a hydrogen atom or a methyl group;
² represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ³ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, And at least one monovalent group selected from the group consisting of an acyl group) and the following general formula 2: (Where R ⁴ represents a hydrogen atom or a methyl group;
⁵ represents at least one monovalent group selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, and an acyl group having 2 to 5 carbon atoms), and the following general formula 3: Formula 7 (Where R ⁶ represents a hydrogen atom or a methyl group;
⁷ represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ⁸ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, At least one monovalent group selected from the group consisting of acyl groups) and at least one radical polymerization selected from the group consisting of compounds represented by the general formula selected from the group consisting of A condensation step of hydrolyzing and condensing using a first silicon compound having a functional group; a polymerization step of subjecting a radical polymerizable group to a radical polymerization reaction during and / or after the condensation step; 100 ° C. to 600 ° C.
A method for producing organic-inorganic composite particles, comprising: a heat treatment step of performing a heat treatment at a temperature of ° C. 7. In the condensation step, if necessary, a general formula 5 together with a radical polymerizable group-containing first silicon compound. (Where X is CH ₂ ＣC (-R ¹ ) -COOR ^2- ,
^{_{CH 2 = C (-R 4)}} - , or ^{_{CH 2 = C (-R 6)}} -R 7
- a monovalent radical-polymerizable functional group represented by; R ¹ and R ⁴ and R ⁶ represents a hydrogen atom or a methyl group; R ² and R ⁷
Represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ⁹ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, R ¹⁰ represents at least one monovalent group selected from the group consisting of an acyl group; R ¹⁰ represents an alkyl group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms, And m represents an integer of 2 to 3; n represents an integer of 0 to 2; m + n represents an integer of 2 to 3; A plurality of Xs may be different from each other, and 2
More than one may be the same. When n is 2, two R
¹⁰ may be different from each other or may be the same. For 4-m-n is 2, the two R ⁹ are may be different from each other, at least one selected from the compounds represented by either the same or) and the group consisting of a derivative thereof, the radical Hydrolysis / condensation using a polymerizable group-containing second silicon compound, and without using a radical polymerizable monomer other than the radical polymerizable group-containing first silicon compound and the radical polymerizable group-containing second silicon compound. The method for producing organic-inorganic composite particles according to claim 6. 8. The following general formula 1: (Where R ¹ represents a hydrogen atom or a methyl group;
² represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ³ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, And at least one monovalent group selected from the group consisting of an acyl group) and the following general formula 2: (Where R ⁴ represents a hydrogen atom or a methyl group;
⁵ represents at least one monovalent group selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, and an acyl group having 2 to 5 carbon atoms), and the following general formula 3: Formula 11 (Where R ⁶ represents a hydrogen atom or a methyl group;
⁷ represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ⁸ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, At least one monovalent group selected from the group consisting of acyl groups) and at least one radical polymerization selected from the group consisting of compounds represented by the general formula selected from the group consisting of A condensation step of hydrolyzing and condensing using a first silicon compound having a functional group; a polymerization step of subjecting a radical polymerizable group to a radical polymerization reaction during and / or after the condensation step; A process of heat-treating the polymer particles in a vacuum at a temperature of 800 ° C. or lower in a vacuum. 9. The following general formula 1: (Where R ¹ represents a hydrogen atom or a methyl group;
² represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ³ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, And at least one monovalent group selected from the group consisting of an acyl group) and the following general formula 2: (Where R ⁴ represents a hydrogen atom or a methyl group;
⁵ represents at least one monovalent group selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, and an acyl group having 2 to 5 carbon atoms), and the following general formula 3: Formula 14 (Where R ⁶ represents a hydrogen atom or a methyl group;
⁷ represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ⁸ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, At least one monovalent group selected from the group consisting of acyl groups) and at least one radical polymerization selected from the group consisting of compounds represented by the general formula selected from the group consisting of Using a first silicon compound having a functional group, if necessary, a compound of the general formula 5 (Where X is CH ₂ ＣC (-R ¹ ) -COOR ^2- ,
^{_{CH 2 = C (-R 4)}} - , or ^{_{CH 2 = C (-R 6)}} -R 7
- a monovalent radical-polymerizable functional group represented by; R ¹ and R ⁴ and R ⁶ represents a hydrogen atom or a methyl group; R ² and R ⁷
Represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ⁹ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, R ¹⁰ represents at least one monovalent group selected from the group consisting of an acyl group; R ¹⁰ represents an alkyl group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms, And m represents an integer of 2 to 3; n represents an integer of 0 to 2; m + n represents an integer of 2 to 3; A plurality of Xs may be different from each other, and 2
More than one may be the same. When n is 2, two R
¹⁰ may be different from each other or may be the same. For 4-m-n is 2, the two R ⁹ are may be different from each other, at least one selected from the compounds represented by either the same or) and the group consisting of a derivative thereof, the radical Using a polymerizable group-containing second silicon compound, and hydrolyzing / condensing a metal compound other than the radical polymerizable group-containing first silicon compound and the radical polymerizable group-containing second silicon compound, the radical polymerizable group 0 to the total weight of the containing first silicon compound and the radical polymerizable group-containing second silicon compound.
A condensation step of hydrolyzing and condensing by using in a range of 200 wt%, a polymerization step of subjecting a radical polymerizable group to a radical polymerization reaction during and / or after the condensation step, and a polymer formed in the polymerization step A method for producing organic-inorganic composite particles, comprising: a heat treatment step of heat-treating the particles at a temperature of 800 ° C. or lower. 10. The following general formula 1: (Where R ¹ represents a hydrogen atom or a methyl group;
² represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ³ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, And at least one monovalent group selected from the group consisting of an acyl group) and the following general formula 2: (Where R ⁴ represents a hydrogen atom or a methyl group;
⁵ represents at least one monovalent group selected from the group consisting of a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, and an acyl group having 2 to 5 carbon atoms), and the following general formula 3: Formula 18 (Where R ⁶ represents a hydrogen atom or a methyl group;
⁷ represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ⁸ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, At least one monovalent group selected from the group consisting of acyl groups) and at least one radical polymerization selected from the group consisting of compounds represented by the general formula selected from the group consisting of Using a first silicon compound having a functional group, if necessary, a compound of the general formula 5 (Where X is CH ₂ ＣC (-R ¹ ) -COOR ^2- ,
^{_{CH 2 = C (-R 4)}} - , or ^{_{CH 2 = C (-R 6)}} -R 7
- a monovalent radical-polymerizable functional group represented by; R ¹ and R ⁴ and R ⁶ represents a hydrogen atom or a methyl group; R ² and R ⁷
Represents a divalent organic group having 1 to 20 carbon atoms which may have a substituent; R ⁹ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, R ¹⁰ represents at least one monovalent group selected from the group consisting of an acyl group; R ¹⁰ represents an alkyl group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms, And m represents an integer of 2 to 3; n represents an integer of 0 to 2; m + n represents an integer of 2 to 3; A plurality of Xs may be different from each other, and 2
More than one may be the same. When n is 2, two R
¹⁰ may be different from each other or may be the same. For 4-m-n is 2, the two R ⁹ are may be different from each other, at least one selected from the compounds represented by either the same or) and the group consisting of a derivative thereof, the radical A radical polymerizable monomer other than the radical polymerizable group-containing first silicon compound and the radical polymerizable group-containing second silicon compound is used by using the radical polymerizable group-containing first silicon compound. 0 to 50 wt% based on the total weight of the compound and the radical polymerizable group-containing second silicon compound
%, A condensation step of performing hydrolysis and condensation, a polymerization step of performing a radical polymerization reaction of a radical polymerizable group during and / or after the condensation step, and a polymer particle formed in the polymerization step. A heat treatment step of heat-treating at a temperature of 800 ° C. or less.