Patent Application
20220213348
The present invention relates to a silicon-containing polymer; a film-forming composition including the silicon-containing polymer;
a method for supporting a metal compound on a surface of an object to be treated by forming a coating film on the surface of the object to be treated using the film-forming composition and bringing the coating film into contact with a metal compound;
an article having a coating film that includes the silicon-containing polymer and supports a metal compound; and a method for producing the silicon-containing polymer.
It is widely known that metal compounds containing various elemental metals have functions as catalysts and functions to adjust various physical properties such as optical properties and electrical conductivity. For this reason, metal compounds may be used not only as substrates, but also as a thin coating on the surface of various articles, in some cases.
With respect to formation of a coating film containing a metal compound, for example, as a pretreatment for forming a diamond-like carbon film, a method is known in which a solution containing one or two or more metal compounds selected from a metal compound containing Ni, a metal compound containing Co, and a metal compound containing Fe is applied to the surface of a substrate comprising Si (See Patent Document 1.).
However, when an aqueous solution of a metal compound is directly applied to the surface of a substrate, as in the method described in Patent Document 1, there is a problem that the metal compound cannot be stably retained on the surface of the substrate or that the amount of the metal compound retained on the surface of the substrate tends to be uneven.
Such a problem can be solved if a coating film capable of supporting a metal compound can be formed on the substrate surface. Generally, to form a coating film, a coating solution containing a polymer is often used. As a chemically stable polymer, silicon-containing polymers such as polysiloxane and polysilane are known.
Under these circumstances, there is a need for a new silicon-containing polymer capable of supporting a metal compound for the purpose of forming a coating film capable of supporting a metal compound containing an elemental metal.
The present invention has been made in view of the above-described problem, and an object of the present invention is to provide a new silicon-containing polymer capable of supporting a metal compound including an elemental metal, a film-forming composition including the silicon-containing polymer;
a method for supporting a metal compound on a surface of an object to be treated by forming a coating film on the surface of the object to be treated using the film-forming composition and bringing the coating film into contact with a metal compound, and bringing the coating film into contact with a metal compound;
an article having a coating film that includes the silicon-containing polymer and supports a metal compound; and a method for producing the silicon-containing polymer.
The present inventors have found that the above problem can be solved by introducing a hydrocarbon group having 1 or more and 10 or less carbon atoms with a cyano group on a silicon atom in a silicon containing polymer containing at least one of a polysiloxane chain or an oligosiloxane chain and a polysilane chain or an oligosilane chain in a molecular chain, and the present invention was completed. More specifically, the present invention provides the following
A first aspect of the present invention relates to a silicon-containing polymer including at least one of poly-siloxane chain or oligo-siloxane chain and poly-silane chain or oligo-silane chain in a molecular chain, in which one or more groups represented by the following formula (1) are bound onto a silicon atom in the silicon-containing polymer;
in which the formula (1) is represented by a following formula:
—R1—CN (1), and
in which, in the formula (1), R1 is a hydrocarbon group having 1 or more and 10 or less carbon atoms.
A second aspect of the present invention relates to a film-forming composition including the silicon-containing polymer (A) as described in the first aspect and a solvent (S).
A third aspect of the present invention relates to a method for supporting a metal compound on a surface of an object to be treated,
the method including:
forming a coated film by applying the film-forming composition as described in the second aspect onto a surface of the object to be treated,
drying the coated film to obtain a coating film including the silicon-containing polymer (A), and bringing the coating film into contact with a metal compound including an elemental metal.
A fourth aspect of the present invention relates to an article having a coating film on a surface thereof, in which the coating film includes the silicon-containing polymer (A) as described in the first aspect, and the coating film supports a metal compound including an elemental metal.
A fifth aspect of the present invention relates to a method for producing polysilane, the polysilane including one or more groups represented by the following formula (1) bound to a silicon atom,
in which the formula (1) is represented by the following formula:
—R1—CN (1)
in which, in the formula (1), R1 is a hydrocarbon group having 1 or more and 10 or less carbon atoms,
the method including homo-polymerizing a cyano group-containing halosilane compound represented by a following formula (1a) in the presence of metallic magnesium, or copolymerizing the cyano group-containing halosilane compound and a halosilane compound other than the cyano group-containing halosilane compound in the presence of metallic magnesium, and
the formula (1a) is represented by the following formula:
R2(2-p)X2Si—(R1—CN)p (1a)
in which in the formula (1a), X is a halogen atom, R1 is the same as the R1 in the formula (1), R2 is a hydrocarbon group having 1 or more and 10 or less carbon atoms, and p is 1 or 2.
According to the present invention, there can be provided a new silicon-containing polymer capable of supporting a metal compound including an elemental metal; a film-forming composition including the silicon-containing polymer; a method for supporting a metal compound on a surface of an object to be treated, the method including forming the coating film on the surface of the object to be treated using the film-forming composition, and bringing the coating film into contact with a metal compound;
an article having a coating film that includes the silicon-containing polymer and supports a metal compound; and a method for producing the silicon-containing polymer.
The silicon-containing polymer includes at least one of poly-siloxane chain or oligo-siloxane chain and poly-silane chain or oligo-silane chain in a molecular chain. In the silicon-containing polymer, one or more groups represented by the following formula (1) are bound onto a silicon atom. The formula (1) is presented by the following formula:
—R1—CN (1).
In the formula (1), R1 is a hydrocarbon group having 1 or more and 10 or less carbon atoms.
The silicon-containing polymer has a group represented by the formula (1). Thereby, by forming a film that contains a silicon-containing polymer on the surface of the object to be treated, a metal compound containing various metal elements can be supported on the surface of the object to be treated.
Due to the ease of producing a silicon-containing polymer and the ease of their utilizing properties as polysilane and polysiloxane, it is preferred that the molecular chain of the silicon-containing polymer consists of only the poly-siloxane chain or the oligo-siloxane chain or consists of only the poly-silane chain or the oligo-silane chain.
The structure of the molecular chain of a silicon-containing polymer is not particularly limited. The structure of the molecular chain may have a linear structure, a branched chain structure, a network structure, or a cyclic structure. Due to the ease of controlling the molecular weights and adjusting various physical properties of a silicon-containing polymer, the structure of the molecular chain of a silicon-containing polymer is preferably linear. It should be noted that the silicon-containing polymer may be combined with a molecule having a different molecular chain structure. The silicon-containing polymer may include, for example, a combination of a linear molecule and a branched molecule.
The poly-siloxane chain or oligo-siloxane chain and the poly-silane chain or oligo-silane chain will now be described.
The structure of poly-siloxane chain or oligo-siloxane chain in a silicon-containing polymer is not particularly limited, so long as the silicon-containing polymer has a group represented by the above formula (1). The poly-siloxane chain or oligo-siloxane chain is preferably, for example, poly-siloxane chain or oligo-siloxane chain obtained by hydrolytic condensation of at least one selected from silane compounds represented by the following formula (A1):
R4-nSi(OR′)n (A1)
In the formula (A1), R represents a hydrogen atom, a group represented by the above formula (1), an aliphatic hydrocarbon group, an aryl group, or an aralkyl group, R′ represents an alkyl group or a phenyl group, and n represents an integer of 2 or more and 4 or less. When a plurality of Rs are bound to Si, the plurality of Rs may be the same or different from each other. A plurality of (OR′) groups bound to Si may also be the same or different from each other.
In addition, the aliphatic hydrocarbon group as R is preferably a linear or branched aliphatic hydrocarbon group having 1 or more and 20 or less carbon atoms, more preferably a linear or branched aliphatic hydrocarbon group having 1 or more and 4 or less carbon atoms. The aliphatic hydrocarbon group as R may have one or more unsaturated bonds. As the aliphatic hydrocarbon group as R, for example, a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a vinyl group, an allyl group, and the like are preferable.
When R is an aryl group or an aralkyl group, the aryl groups contained in these groups are not particularly limited, so long as the object of the present invention is not defeated. Suitable examples of the aryl group include the following groups.
Among the groups represented by the above formulae, the groups represented by the following formulae are preferable.
In the above formulae, Ra1 is a hydrogen atom; a hydroxy group; an alkoxy group such as a methoxy group, an ethoxy group, a butoxy group, or a propoxy group; or a hydrocarbon group such as a methyl group, an ethyl group, a butyl group, or a propyl group. In the above formulae, Ra2 is an alkylene group such as a methylene group, an ethylene group, a propylene group, or a butylene group.
When R is an aryl group or an aralkyl group, suitable specific examples include a benzyl group, a phenethyl group, a phenyl group, a naphthyl group, an anthracenyl group, a phenanthryl group, a biphenylyl group, a fluorenyl group, a pyrenyl group, and the like.
The number of benzene rings in the aryl group or the aralkyl group is preferably 1 to 3. When the number of benzene rings is 1 to 3, it is easy to form a poly-siloxane chain or oligo-siloxane chain. The aryl group or the aralkyl group may have a hydroxy group as a substituent.
The alkyl group as R′ is preferably a linear or branched alkyl group having 1 or more and 5 or less carbon atoms. The number of carbon atoms in the alkyl group as R′ is preferably 1 or 2, particularly in terms of the hydrolysis rate. When n is 4 in the formula (A1), the resulting silane compound (i) is represented by the following formula (A2).
Si(ORA1)a(ORA2)b(ORA3)c(ORA4)d (A2)
In the formula (A2), RA1, RA2, RA3, and RA4 each independently represent the same alkyl group or phenyl group as in R′ above.
a, b, c, and d are integers that satisfy 0≤a≤4, 0≤b≤4, 0≤c≤4, 0≤d≤4, and a+b+c+d=4.
When n is 3 in the formula (A1), the resulting silane compound (ii) is represented by the following formula (A3).
RA5Si(ORA6)e(ORA7)f(ORA8)g (A3)
In the formula (A3), RAS represents a hydrogen atom, a group represented by the above formula (1), or the same aliphatic hydrocarbon group, aryl group, or aralkyl group as in R above. RA6, RA7, and RA8 each independently represent the same alkyl group or phenyl group as in R′ above.
e, f, and g are integers that satisfy 0≤e≤3, 0≤f≤3, 0≤g≤3, and e+f+g=3.
When n is 2 in the formula (A1), the resulting silane compound (iii) is represented by the following formula (A4).
RA9RA10Si(ORA11)h(ORA12)i (A4)
In the formula (A4), RA9 and RA10 represent a hydrogen atom, a group represented by the above formula (1), or the same aliphatic hydrocarbon group, aryl group, or aralkyl group as in R above. RA11 and RA12 each independently represent the same alkyl group or phenyl group as in R′ above.
h and i are integers that satisfy 0≤h≤2, 0≤i≤2, and h+i=2.
Specific examples of the silane compound (i) include tetraalkoxysilanes such as tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, tetrabutoxysilane, tetrapentyloxysilane, tetraphenyloxysilane, trimethoxymonoethoxysilane, dimethoxydiethoxysilane, triethoxymonomethoxysilane, trimethoxymonopropoxysilane, monomethoxytributoxysilane, monomethoxytripentyloxysilane, monomethoxytriphenyloxysilane, dimethoxydipropoxysilane, tripropoxymonomethoxysilane, trimethoxymonobutoxysilane, dimethoxydibutoxysilane, triethoxymonopropoxysilane, diethoxydipropoxysilane, tributoxymonopropoxysilane, dimethoxymonoethoxymonobutoxysilane, diethoxymonomethoxymonobutoxysilane, diethoxymonopropoxymonobutoxysilane, dipropoxymonomethoxymonoethoxysilane, dipropoxymonomethoxymonobutoxysilane, dipropoxymonoethoxymonobutoxysilane, dibutoxymonomethoxymonoethoxysilane, dibutoxymonoethoxymonopropoxysilane, and monomethoxymonoethoxymonopropoxymonobutoxysilane. Among these, tetramethoxysilane and tetraethoxysilane are preferable.
Specific examples of the silane compound (ii) include hydrosilane compounds such as trimethoxysilane, triethoxysilane, tripropoxysilane, tripentyloxysilane, triphenyloxysilane, dimethoxymonoethoxysilane, diethoxymonomethoxysilane, dipropoxymonomethoxysilane, dipropoxymonoethoxysilane, dipentyloxylmonomethoxysilane, dipentyloxymonoethoxysilane, dipentyloxymonopropoxysilane, diphenyloxylmonomethoxysilane, diphenyloxymonoethoxysilane, diphenyloxymonopropoxysilane, methoxyethoxypropoxysilane, monopropoxydimethoxysilane, monopropoxydiethoxysilane, monobutoxydimethoxysilane, monopentyloxydiethoxysilane, and monophenyloxydiethoxysilane; methylsilane compounds such as methyltrimethoxysilane, methyltriethoxysilane, methyltripropoxysilane, methyltripentyloxysilane, methyltriphenyloxysilane, methylmonomethoxydiethoxysilane, methylmonomethoxydipropoxysilane, methylmonomethoxydipentyloxysilane, methylmonomethoxydiphenyloxysilane, methylmethoxyethoxypropoxysilane, and methylmonomethoxymonoethoxymonobutoxysilane; ethylsilane compounds such as ethyltrimethoxysilane, ethyltriethoxysilane, ethyltripropoxysilane, ethyltripentyloxysilane, ethyltriphenyloxysilane, ethylmonomethoxydiethoxysilane, ethylmonomethoxydipropoxysilane, ethylmonomethoxydipentyloxysilane, ethylmonomethoxydiphenyloxysilane, ethylmethoxyethoxypropoxysilane, and ethylmonomethoxymonoethoxymonobutoxysilane; propylsilane compounds such as propyltrimethoxysilane, propyltriethoxysilane, propyltripropoxysilane, propyltripentyloxysilane, and propyltriphenyloxysilane, propylmonomethoxydiethoxysilane, propylmonomethoxydipropoxysilane, propylmonomethoxydipentyloxysilane, propylmonomethoxydiphenyloxysilane, propylmethoxyethoxypropoxysilane, and propylmonomethoxymonoethoxymonobutoxysilane; butylsilane compounds such as butyltrimethoxysilane, butyltriethoxysilane, butyltripropoxysilane, butyltripentyloxysilane, butyltriphenyloxysilane, butylmonomethoxydiethoxysilane, butylmonomethoxydipropoxysilane, butylmonomethoxydipentyloxysilane, butylmonomethoxydiphenyloxysilane, butylmethoxyethoxypropoxysilane, and butylmonomethoxymonoethoxymonobutoxysilane; phenylsilane compounds such as phenyltrimethoxysilane, phenyltriethoxysilane, phenyltripropoxysilane, phenyltripentyloxysilane, phenyltriphenyloxysilane, phenylmonomethoxydiethoxysilane, phenylmonomethoxydipropoxysilane, phenylmonomethoxydipentyloxysilane, phenylmonomethoxydiphenyloxysilane, phenylmethoxyethoxypropoxysilane, and phenylmonomethoxymonoethoxymonobutoxysilane; hydroxyphenylsilane compounds such as hydroxyphenyltrimethoxysilane, hydroxyphenyltriethoxysilane, hydroxyphenyltripropoxysilane, hydroxyphenyltripentyloxysilane, hydroxyphenyltriphenyloxysilane, hydroxyphenylmonomethoxydiethoxysilane, hydroxyphenylmonomethoxydipropoxysilane, hydroxyphenylmonomethoxydipentyloxysilane, hydroxyphenylmonomethoxydiphenyloxysilane, hydroxyphenylmethoxyethoxypropoxysilane, and hydroxyphenylmonomethoxymonoethoxymonobutoxysilane; naphthylsilane compounds such as naphthyltrimethoxysilane, naphthyltriethoxysilane, naphthyltripropoxysilane, naphthyltripentyloxysilane, naphthyltriphenyloxysilane, naphthylmonomethoxydiethoxysilane, naphthylmonomethoxydipropoxysilane, naphthylmonomethoxydipentyloxysilane, naphthylmonomethoxydiphenyloxysilane, naphthylmethoxyethoxypropoxysilane, and naphthylmonomethoxymonoethoxymonobutoxysilane; benzylsilane compounds such as benzyltrimethoxysilane, benzyltriethoxysilane, benzyltripropoxysilane, benzyltripentyloxysilane, benzyltriphenyloxysilane, benzylmonomethoxydiethoxysilane, benzylmonomethoxydipropoxysilane, benzylmonomethoxydipentyloxysilane, benzylmonomethoxydiphenyloxysilane, benzylmethoxyethoxypropoxysilane, and benzylmonomethoxymonoethoxymonobutoxysilane; hydroxybenzylsilane compounds such as hydroxybenzyltrimethoxysilane, hydroxybenzyltriethoxysilane, hydroxybenzyltripropoxysilane, hydroxybenzyltripentyloxysilane, hydroxybenzyltriphenyloxysilane, hydroxybenzylmonomethoxydiethoxysilane, hydroxybenzylmonomethoxydipropoxysilane, hydroxybenzylmonomethoxydipentyloxysilane, hydroxybenzylmonomethoxydiphenyloxysilane, hydroxybenzylmethoxyethoxypropoxysilane, and hydroxybenzylmonomethoxymonoethoxymonobutoxysilane; vinylsilane compounds such as vinyltrimethoxysilane, vinyltriethoxysilane, vinyltripropoxysilane, vinyltripentyloxysilane, vinyltriphenyloxysilane, vinylmonomethoxydiethoxysilane, vinylmonomethoxydipropoxysilane, vinylmonomethoxydipentyloxysilane, vinylmonomethoxydiphenyloxysilane, vinylmethoxyethoxypropoxysilane, and vinylmonomethoxymonoethoxymonobutoxysilane; and allylsilane compounds such as allyltrimethoxysilane, allyltriethoxysilane, allyltripropoxysilane, allyltripentyloxysilane, allyltriphenyloxysilane, allylmonomethoxydiethoxysilane, allylmonomethoxydipropoxysilane, allylmonomethoxydipentyloxysilane, allylmonomethoxydiphenyloxysilane, allylmethoxyethoxypropoxysilane, and allylmonomethoxymonoethoxymonobutoxysilane.
Compounds obtained by substituting a methyl group, an ethyl group, a propyl group, a butyl group, a hydroxyphenyl group, a naphthyl group, a benzyl group, a hydroxybenzyl group, a vinyl group, or an allyl group in the above compounds with a group represented by the above formula (1) are also preferable as the silane compound (ii).
Specific examples of the silane compound (iii) include hydrosilane compounds such as dimethoxysilane, diethoxysilane, dipropoxysilane, dipentyloxysilane, diphenyloxysilane, methoxyethoxysilane, methoxypropoxysilane, methoxypentyloxysilane, methoxyphenyloxysilane, ethoxypropoxysilane, ethoxypentyloxysilane, and ethoxyphenyloxysilane; methylhydrosilane compounds such as methyldimethoxysilane, methylmethoxyethoxysilane, methyldiethoxysilane, methylmethoxypropoxysilane, methylmethoxypentyloxysilane, methylethoxypropoxysilane, methyldipropoxysilane, methyldipentyloxysilane, methyldiphenyloxysilane, and methylmethoxyphenyloxysilane; ethylhydrosilane compounds such as ethyldimethoxysilane, ethylmethoxyethoxysilane, ethyldiethoxysilane, ethylmethoxypropoxysilane, ethylmethoxypentyloxysilane, ethylethoxypropoxysilane, ethyldipropoxysilane, ethyldipentyloxysilane, ethyldiphenyloxysilane, and ethylmethoxyphenyloxysilane; propylhydrosilane compounds such as propyldimethoxysilane, propylmethoxyethoxysilane, propyldiethoxysilane, propylmethoxypropoxysilane, propylmethoxypentyloxysilane, propylethoxypropoxysilane, propyldipropoxysilane, propyldipentyloxysilane, propyldiphenyloxysilane, and propylmethoxyphenyloxysilane; butylhydrosilane compounds such as butyldimethoxysilane, butylmethoxyethoxysilane, butyldiethoxysilane, butylmethoxypropoxysilane, butylmethoxypentyloxysilane, butylethoxypropoxysilane, butyldipropoxysilane, butyldipentyloxysilane, butyldiphenyloxysilane, and butylmethoxyphenyloxysilane; phenylhydrosilane compounds such as phenyldimethoxysilane, phenylmethoxyethoxysilane, phenyldiethoxysilane, phenylmethoxypropoxysilane, phenylmethoxypentyloxysilane, phenylethoxypropoxysilane, phenyldipropoxysilane, phenyldipentyloxysilane, phenyldiphenyloxysilane, and phenylmethoxyphenyloxysilane; hydroxyphenylhydrosilane compounds such as hydroxyphenyldimethoxysilane, hydroxyphenylmethoxyethoxysilane, hydroxyphenyldiethoxysilane, hydroxyphenylmethoxypropoxysilane, hydroxyphenylmethoxypentyloxysilane, hydroxyphenylethoxypropoxysilane, hydroxyphenyldipropoxysilane, hydroxyphenyldipentyloxysilane, hydroxyphenyldiphenyloxysilane, and hydroxyphenylmethoxyphenyloxysilane; naphthylhydrosilane compounds such as naphthyldimethoxysilane, naphthylmethoxyethoxysilane, naphthyldiethoxysilane, naphthylmethoxypropoxysilane, naphthylmethoxypentyloxysilane, naphthylethoxypropoxysilane, naphthyldipropoxysilane, naphthyldipentyloxysilane, naphthyldiphenyloxysilane, and naphthylmethoxyphenyloxysilane; benzylhydrosilane compounds such as benzyldimethoxysilane, benzylmethoxyethoxysilane, benzyldiethoxysilane, benzylmethoxypropoxysilane, benzylmethoxypentyloxysilane, benzylethoxypropoxysilane, benzyldipropoxysilane, benzyldipentyloxysilane, benzyldiphenyloxysilane, and benzylmethoxyphenyloxysilane; hydroxybenzylhydrosilane compounds such as hydroxybenzyldimethoxysilane, hydroxybenzylmethoxyethoxysilane, hydroxybenzyldiethoxysilane, hydroxybenzylmethoxypropoxysilane, hydroxybenzylmethoxypentyloxysilane, hydroxybenzylethoxypropoxysilane, hydroxybenzyldipropoxysilane, hydroxybenzyldipentyloxysilane, hydroxybenzyldiphenyloxysilane, and hydroxybenzylmethoxyphenyloxysilane; dimethylsilane compounds such as dimethyldimethoxysilane, dimethylmethoxyethoxysilane, dimethylmethoxypropoxysilane, dimethyldiethoxysilane, dimethyldipentyloxysilane, dimethyldiphenyloxysilane, dimethylethoxypropoxysilane, and dimethyldipropoxysilane; diethylsilane compounds such as diethyldimethoxysilane, diethylmethoxyethoxysilane, diethylmethoxypropoxysilane, diethyldiethoxysilane, diethyldipentyloxysilane, diethyldiphenyloxysilane, diethylethoxypropoxysilane, and diethyldipropoxysilane; dipropoxysilane compounds such as dipropyldimethoxysilane, dipropylmethoxyethoxysilane, dipropylmethoxypropoxysilane, dipropyldiethoxysilane, dipropyldipentyloxysilane, dipropyldiphenyloxysilane, dipropylethoxypropoxysilane, and dipropyldipropoxysilane; dibutylsilane compounds such as dibutyldimethoxysilane, dibutylmethoxyethoxysilane, dibutylmethoxypropoxysilane, dibutyldiethoxysilane, dibutyldipentyloxysilane, dibutyldiphenyloxysilane, dibutylethoxypropoxysilane, and dibutyldipropoxysilane; diphenylsilane compounds such as diphenyldimethoxysilane, diphenylmethoxyethoxysilane, diphenylmethoxypropoxysilane, diphenyldiethoxysilane, diphenyldipentyloxysilane, diphenyldiphenyloxysilane, diphenylethoxypropoxysilane, and diphenyldipropoxysilane; di(hydroxyphenyl)silane compounds such as di(hydroxyphenyl)dimethoxysilane, di(hydroxyphenyl)methoxyethoxysilane, di(hydroxyphenyl)methoxypropoxysilane, di(hydroxyphenyl)diethoxysilane, di(hydroxyphenyl)dipentyloxysilane, di(hydroxyphenyl)diphenyloxysilane, di(hydroxyphenyl)ethoxypropoxysilane, and di(hydroxyphenyl)dipropoxysilane; dinaphthylsilane compounds such as dinaphthyldimethoxysilane, dinaphthylmethoxyethoxysilane, dinaphthylmethoxypropoxysilane, dinaphthyldiethoxysilane, dinaphthyldipentyloxysilane, dinaphthyldiphenyloxysilane, dinaphthylethoxypropoxysilane, and dinaphthyldipropoxysilane; dibenzylsilane compounds such as dibenzyldimethoxysilane, dibenzylmethoxyethoxysilane, dibenzylmethoxypropoxysilane, dibenzyldiethoxysilane, dibenzyldipentyloxysilane, dibenzyldiphenyloxysilane, dibenzylethoxypropoxysilane, and dibenzyldipropoxysilane; di(hydroxybenzyl)silane compounds such as di(hydroxybenzyl)dimethoxysilane, di(hydroxybenzyl)methoxyethoxysilane, di(hydroxybenzyl)methoxypropoxysilane, di(hydroxybenzyl)diethoxysilane, di(hydroxybenzyl)dipentyloxysilane, di(hydroxybenzyl)diphenyloxysilane, di(hydroxybenzyl)ethoxypropoxysilane, and di(hydroxybenzyl)dipropoxysilane; methylethylsilane compounds such as methylethyldimethoxysilane, methylethylmethoxyethoxysilane, methylethylmethoxypropoxysilane, methylethyldiethoxysilane, methylethyldipentyloxysilane, methylethyldiphenyloxysilane, methylethylethoxypropoxysilane, and methylethyldipropoxysilane; methylpropylsilane compounds such as methylpropyldimethoxysilane, methylpropylmethoxyethoxysilane, methylpropylmethoxypropoxysilane, methylpropyldiethoxysilane, methylpropyldipentyloxysilane, methylpropyldiphenyloxysilane, methylpropylethoxypropoxysilane, and methylpropyldipropoxysilane; methylbutylsilane compounds such as methylbutyldimethoxysilane, methylbutylmethoxyethoxysilane, methylbutylmethoxypropoxysilane, methylbutyldiethoxysilane, methylbutyldipentyloxysilane, methylbutyldiphenyloxysilane, methylbutylethoxypropoxysilane, and methylbutyldipropoxysilane; methyl(phenyl)silane compounds such as methyl(phenyl)dimethoxysilane, methyl(phenyl)methoxyethoxysilane, methyl(phenyl)methoxypropoxysilane, methyl(phenyl)diethoxysilane, methyl(phenyl)dipentyloxysilane, methyl(phenyl)diphenyloxysilane, methyl(phenyl)ethoxypropoxysilane, and methyl(phenyl)dipropoxysilane; methyl(hydroxyphenyl)silane compounds such as methyl(hydroxyphenyl)dimethoxysilane, methyl(hydroxyphenyl)methoxyethoxysilane, methyl(hydroxyphenyl)methoxypropoxysilane, methyl(hydroxyphenyl)diethoxysilane, methyl(hydroxyphenyl)dipentyloxysilane, methyl(hydroxyphenyl)diphenyloxysilane, methyl(hydroxyphenyl)ethoxypropoxysilane, and methyl(hydroxyphenyl)dipropoxysilane; methyl(naphthyl)silane compounds such as methyl(naphthyl)dimethoxysilane, methyl(naphthyl)methoxyethoxysilane, methyl(naphthyl)methoxypropoxysilane, methyl(naphthyl)diethoxysilane, methyl(naphthyl)dipentyloxysilane, methyl(naphthyl)diphenyloxysilane, methyl(naphthyl)ethoxypropoxysilane, and methyl(naphthyl)dipropoxysilane; methyl(benzyl)silane compounds such as methyl(benzyl)dimethoxysilane, methyl(benzyl)methoxyethoxysilane, methyl(benzyl)methoxypropoxysilane, methyl(benzyl)diethoxysilane, methyl(benzyl)dipentyloxysilane, methyl(benzyl)diphenyloxysilane, methyl(benzyl)ethoxypropoxysilane, and methyl(benzyl)dipropoxysilane; methyl(hydroxybenzyl)silane compounds such as methyl(hydroxybenzyl)dimethoxysilane, methyl(hydroxybenzyl)methoxyethoxysilane, methyl(hydroxybenzyl)methoxypropoxysilane, methyl(hydroxybenzyl)diethoxysilane, methyl(hydroxybenzyl)dipentyloxysilane, methyl(hydroxybenzyl)diphenyloxysilane, methyl(hydroxybenzyl)ethoxypropoxysilane, and methyl(hydroxybenzyl)dipropoxysilane; ethylpropylsilane compounds such as ethylpropyldimethoxysilane, ethylpropylmethoxyethoxysilane, ethylpropylmethoxypropoxysilane, ethylpropyldiethoxysilane, ethylpropyldipentyloxysilane, ethylpropyldiphenyloxysilane, ethylpropylethoxypropoxysilane, and ethylpropyldipropoxysilane; ethylbutylsilane compounds such as ethylbutyldimethoxysilane, ethylbutylmethoxyethoxysilane, ethylbutylmethoxypropoxysilane, ethylbutyldiethoxysilane, ethylbutyldipentyloxysilane, ethylbutyldiphenyloxysilane, ethylbutylethoxypropoxysilane, and ethylbutyldipropoxysilane; ethyl(phenyl)silane compounds such as ethyl(phenyl)dimethoxysilane, ethyl(phenyl)methoxyethoxysilane, ethyl(phenyl)methoxypropoxysilane, ethyl(phenyl)diethoxysilane, ethyl(phenyl)dipentyloxysilane, ethyl(phenyl)diphenyloxysilane, ethyl(phenyl)ethoxypropoxysilane, and ethyl(phenyl)dipropoxysilane; ethyl(hydroxyphenyl)silane compounds such as ethyl(hydroxyphenyl)dimethoxysilane, ethyl(hydroxyphenyl)methoxyethoxysilane, ethyl(hydroxyphenyl)methoxypropoxysilane, ethyl(hydroxyphenyl)diethoxysilane, ethyl(hydroxyphenyl)dipentyloxysilane, ethyl(hydroxyphenyl)diphenyloxysilane, ethyl(hydroxyphenyl)ethoxypropoxysilane, and ethyl(hydroxyphenyl)dipropoxysilane; ethyl(naphthyl)silane compounds such as ethyl(naphthyl)dimethoxysilane, ethyl(naphthyl)methoxyethoxysilane, ethyl(naphthyl)methoxypropoxysilane, ethyl(naphthyl)diethoxysilane, ethyl(naphthyl)dipentyloxysilane, ethyl(naphthyl)diphenyloxysilane, ethyl(naphthyl)ethoxypropoxysilane, and ethyl(naphthyl)dipropoxysilane; ethyl(benzyl)silane compounds such as ethyl(benzyl)dimethoxysilane, ethyl(benzyl)methoxyethoxysilane, ethyl(benzyl)methoxypropoxysilane, ethyl(benzyl)diethoxysilane, ethyl(benzyl)dipentyloxysilane, ethyl(benzyl)diphenyloxysilane, ethyl(benzyl)ethoxypropoxysilane, and ethyl(benzyl)dipropoxysilane; ethyl(hydroxybenzyl)silane compounds such as ethyl(hydroxybenzyl)dimethoxysilane, ethyl(hydroxybenzyl)methoxyethoxysilane, ethyl(hydroxybenzyl)methoxypropoxysilane, ethyl(hydroxybenzyl)diethoxysilane, ethyl(hydroxybenzyl)dipentyloxysilane, ethyl(hydroxybenzyl)diphenyloxysilane, ethyl(hydroxybenzyl)ethoxypropoxysilane, and ethyl(hydroxybenzyl)dipropoxysilane; propylbutylsilane compounds such as propylbutyldimethoxysilane, propylbutylmethoxyethoxysilane, propylbutylmethoxypropoxysilane, propylbutyldiethoxysilane, propylbutyldipentyloxysilane, propylbutyldiphenyloxysilane, propylbutylethoxypropoxysilane, and propylbutyldipropoxysilane; propyl(phenyl)silane compounds such as propyl(phenyl)dimethoxysilane, propyl(phenyl)methoxyethoxysilane, propyl(phenyl)methoxypropoxysilane, propyl(phenyl)diethoxysilane, propyl(phenyl)dipentyloxysilane, propyl(phenyl)diphenyloxysilane, propyl(phenyl)ethoxypropoxysilane, and propyl(phenyl)dipropoxysilane; propyl(hydroxyphenyl)silane compounds such as propyl(hydroxyphenyl)dimethoxysilane, propyl(hydroxyphenyl)methoxyethoxysilane, propyl(hydroxyphenyl)methoxypropoxysilane, propyl(hydroxyphenyl)diethoxysilane, propyl(hydroxyphenyl)dipentyloxysilane, propyl(hydroxyphenyl)diphenyloxysilane, propyl(hydroxyphenyl)ethoxypropoxysilane, and propyl(hydroxyphenyl)dipropoxysilane; propyl(naphthyl)silane compounds such as propyl(naphthyl)dimethoxysilane, propyl(naphthyl)methoxyethoxysilane, propyl(naphthyl)methoxypropoxysilane, propyl(naphthyl)diethoxysilane, propyl(naphthyl)dipentyloxysilane, propyl(naphthyl)diphenyloxysilane, propyl(naphthyl)ethoxypropoxysilane, and propyl(naphthyl)dipropoxysilane; propyl(benzyl)silane compounds such as propyl(benzyl)dimethoxysilane, propyl(benzyl)methoxyethoxysilane, propyl(benzyl)methoxypropoxysilane, propyl(benzyl)diethoxysilane, propyl(benzyl)dipentyloxysilane, propyl(benzyl)diphenyloxysilane, propyl(benzyl)ethoxypropoxysilane, and propyl(benzyl)dipropoxysilane; propyl(hydroxybenzyl)silane compounds such as propyl(hydroxybenzyl)dimethoxysilane, propyl(hydroxybenzyl)methoxyethoxysilane, propyl(hydroxybenzyl)methoxypropoxysilane, propyl(hydroxybenzyl)diethoxysilane, propyl(hydroxybenzyl)dipentyloxysilane, propyl(hydroxybenzyl)diphenyloxysilane, propyl(hydroxybenzyl)ethoxypropoxysilane, and propyl(hydroxybenzyl)dipropoxysilane; divinylsilane compounds such as divinyldimethoxysilane, divinylmethoxyethoxysilane, divinylmethoxypropoxysilane, divinyldiethoxysilane, divinyldipentyloxysilane, divinyldiphenyloxysilane, divinylethoxypropoxysilane, and divinyldipropoxysilane; vinylmethylsilane compounds such as vinylmethyldimethoxysilane, vinylmethylmethoxyethoxysilane, vinylmethylmethoxypropoxysilane, vinylmethyldiethoxysilane, vinylmethyldipentyloxysilane, vinylmethyldiphenyloxysilane, vinylmethylethoxypropoxysilane, and vinylmethyldipropoxysilane; vinylethylsilane compounds such as vinylethyldimethoxysilane, vinylethylmethoxyethoxysilane, vinylethylmethoxypropoxysilane, vinylethyldiethoxysilane, vinylethyldipentyloxysilane, vinylmethyldiphenyloxysilane, vinylethylethoxypropoxysilane, and vinylethyldipropoxysilane; vinyl(phenyl)silane compounds such as vinyl(phenyl)dimethoxysilane, vinyl(phenyl)methoxyethoxysilane, vinyl(phenyl)methoxypropoxysilane, vinyl(phenyl)diethoxysilane, vinyl(phenyl)dipentyloxysilane, vinyl(phenyl)diphenyloxysilane, vinyl(phenyl)ethoxypropoxysilane, and vinyl(phenyl)dipropoxysilane; diallylsilane compounds such as diallyldimethoxysilane, diallylmethoxyethoxysilane, diallylmethoxypropoxysilane, diallyldiethoxysilane, diallyldipentyloxysilane, diallyldiphenyloxysilane, diallylethoxypropoxysilane, and diallyldipropoxysilane; allylmethylsilane compounds such as allylmethyldimethoxysilane, allylmethylmethoxyethoxysilane, allylmethylmethoxypropoxysilane, allylmethyldiethoxysilane, allylmethyldipentyloxysilane, allylmethyldiphenyloxysilane, allylmethylethoxypropoxysilane, and allylmethyldipropoxysilane; allylethylsilane compounds such as allylethyldimethoxysilane, allylethylmethoxyethoxysilane, allylethylmethoxypropoxysilane, allylethyldiethoxysilane, allylethyldipentyloxysilane, allylmethyldiphenyloxysilane, allylethylethoxypropoxysilane, and allylethyldipropoxysilane; allyl(phenyl)silane compounds such as allyl(phenyl)dimethoxysilane, allyl(phenyl)methoxyethoxysilane, allyl(phenyl)methoxypropoxysilane, allyl(phenyl)diethoxysilane, allyl(phenyl)dipentyloxysilane, allyl(phenyl)diphenyloxysilane, allyl(phenyl)ethoxypropoxysilane, and allyl(phenyl)dipropoxysilane.
Compounds obtained by substituting at least one of methyl groups, ethyl groups, propyl groups, butyl groups, hydroxyphenyl groups, naphthyl groups, benzyl groups, hydroxybenzyl groups, vinyl groups, and allyl groups in the above compounds with a group represented by the above formula (1) are also preferable as the silane compound (iii).
By subjecting a silane compound described above to hydrolytic condensation by a conventional procedure, the poly-siloxane chain or oligo-siloxane chain is formed.
As the poly-siloxane chain or oligo-siloxane chain, a siloxane chain including a unit represented by the following formula (A3-1) and/or a unit represented by the following formula (A4-1) is preferable, and a linear siloxane chain including a unit represented by the formula (A4-1) is more preferable:
—(SiRA13O3/2)— (A3-1)
—(SiRA14RA15O2/2)— (A4-1)
In the formula (A3-1) and the formula (A4-1), RA13, RA14 and RA15 are each independently a group represented by the above formula (1), a linear or branched alkyl group having 1 or more and 4 or less carbon atoms, or a phenyl group.
The structure of poly-silane chain or oligo-silane chain in a silicon-containing polymer is not particularly limited, so long as the silicon-containing polymer has a group represented by the above formula (1). The poly-silane chain or oligo-silane chain may include a silanol group and/or an alkoxy group. The poly-silane chain or oligo-silane chain is preferably formed from, for example, at least one of units represented by the following formulae (A5) to (A7):
(In the formulae (A5), (A7), and (A8), Ra3 and Ra4 each represent a hydrogen atom, an organic group, or a silyl group. Ra5 represents a hydrogen atom or an alkyl group. When Ra5 is an alkyl group, an alkyl group having 1 or more and 4 or less carbon atoms is preferable, a methyl group and an ethyl group are more preferable.).
As the alkyl group as Rai and Rao, a carbon atom-containing group is preferred, and a group including one or more carbon atoms and at least one atom selected from the group consisting of H, O, S, Se, N, B, P, and halogen atoms is more preferred. Examples of the organic groups as Rai and Rao include a group represented by the above-described formula (1), hydrocarbon groups such as an alkyl group, an alkenyl group, a cycloalkyl group, a cycloalkenyl group, an aryl group, and an aralkyl group, an alkoxy group, an alkenyloxy group, a cycloalkoxy group, a cycloalkenyloxy group, an aryloxy group, and an aralkyloxy group, and the like. Among these groups, a group represented by the above-described formula (1), an alkyl group, an aryl group, and an aralkyl group are preferable. Suitable examples of the alkyl group, aryl group and aralkyl group are the same as in the case where R is an alkyl group, an aryl group, or an aralkyl group in the above-described formula (A1).
When Ra3 and Ra4 are each a silyl group, examples of the silyl group include a silyl group and Si1-10 silanyl groups (such as Si1-5 silanyl groups) such as a disilanyl group and a trisilanyl group. The poly-silane chain or oligo-silane chain preferably includes units of the following formulae (A10) to (A13).
In (A10) to (A13), Ra3 and Rao are the same as Rai and Rao in the formulae (A5), (A7), and (A8). Each of a, b, and c is an integer of 2 to 1000. Each of a, b, and c is preferably 10 to 500, more preferably 10 to 100. The building block in each unit may be present in the unit either in a random manner or in a blocked state.
Among the poly-silane chain or oligo-silane chains described above, poly-silane chain or oligo-silane chain including a combination of a group represented by the formula (1), an alkyl group, and an aryl group or an aralkyl group, each bound to a silicon atom, and poly-silane chain or oligo-silane chain including a combination of a group represented by the formula (1) and an alkyl group, each bound to a silicon atom, are preferable.
More specifically, poly-silane chain or oligo-silane chain including a combination of a group represented by the formula (1), a methyl group, and a benzyl group each bound to a silicon atom, poly-silane chain or oligo-silane chain including a combination of a group represented by the formula (1), a methyl group, and a phenyl group, each bound to a silicon atom, poly-silane chain or oligo-silane chain including a combination of a group represented by the formula (1) and a methyl group, each bound to a silicon atom, and poly-silane chain or oligo-silane chain including only groups represented by the formula (1), each bound to a silicon atom, are preferably used.
The silicon-containing polymer has a group represented by the formula (1) and thereby can support a metal compound including various elemental metals.
The number of moles of a group represented by the formula (1) in the silicon-containing polymer is preferably 0.05 mol or more and 2.0 mol or less and more preferably 0.2 mol or more and 1.0 mol or less with respect to 1 mol of silicon atom in the silicon-containing polymer because the silicon-containing polymer easily supports a metal compound in a satisfactory manner.
The hydrocarbon group as R1 in the above formula (1) is not particularly limited, so long as the number of carbon atoms is 1 or more and 10 or less. The hydrocarbon group as R1 may be an aliphatic hydrocarbon group, an aromatic hydrocarbon group, or a combination of an aliphatic hydrocarbon group and an aromatic hydrocarbon group.
In cases where the hydrocarbon group as R1 is an aliphatic hydrocarbon group and the hydrocarbon group as R1 includes an aliphatic hydrocarbon group, the aliphatic hydrocarbon group may be linear or branched or include a cyclic skeleton. From the viewpoint that raw materials are easily acquired and the viewpoint that the silicon-containing polymer easily supports a metal compound, which will be described below, the hydrocarbon group as R1 is preferably a linear or branched hydrocarbon group, and more preferably a linear hydrocarbon group.
While the groups represented by the formula (1) are unlikely to sterically interfere with each other because the chain length is not too long, degree of freedom in the steric conformation of the groups represented by the formula (1) is high because the chain length is long to an extent. From such a viewpoint, as the hydrocarbon group as R1, an alkylene group having 2 or more and 8 or less carbon atoms is preferable, a linear alkylene group having 2 or more and 8 or less carbon atoms is more preferable, and a linear alkylene group having 2 or more and 6 or less carbon atoms is the most preferable.
Specific examples of the hydrocarbon groups as R1 include a methylene group, an ethane-1,2-diyl group, an ethane-1,1-diyl group, a propane-1,3-diyl group, a propane-1,2-diyl group, a propane-1,1-diyl group, a butane-1,4-diyl group, a pentane-1,5-diyl group, a hexane-1,6-diyl group, a heptane-1,7-diyl group, an octane-1,8-diyl group, a nonane-1,9-diyl group, a decane-1,10-diyl group, a cyclohexane-1,4-diyl group, a cyclohexane-1,3-diyl group, a cyclohexane-1,2-diyl group, a p-phenylene group, a m-phenylene group, an o-phenylene group, a naphthalene-2,6-diyl group, a naphthalene-2,7-diyl group, and a naphthalene-1,4-diyl group, and the like.
Among the above hydrocarbon groups as R1, an ethane-1,2-diyl group, a propane-1,3-diyl group, a p-phenylene group, and a m-phenylene group are preferable, and an ethane-1,2-diyl group, and a propane-1,3-diyl group are more preferable.
As the group represented by the formula (1), a cyanomethyl group, a 2-cyanoethyl group, a 3-cyano-n-propyl group, a 4-cyano-n-butyl group, a 5-cyano-n-pentyl group, and a 6-cyano-n-pentyl group are preferable, and a 2-cyanoethyl group, a 3-cyano-n-propyl group, and a 4-cyano-n-butyl group are more preferred.
The weight average molecular weight (Mw) of a silicon-containing polymer described above, and the dispersion degree (Mw/Mn), the ratio of weight average molecular weight (Mw) and number average molecular weight (Mn), are not particularly limited. The weight average molecular weight is preferably 500 or more and 12000 or less, more preferably 700 or more and 8000 or less, and further preferably 700 or more and 3000 or less from the viewpoint of solubility in the film-forming composition or film forming properties. The dispersion degree is preferably 1 or more and 4.5 or less, and more preferably 2 or more and 4 or less.
The film-forming composition includes the above-described silicon-containing polymer (A) and a solvent (S). By applying such a film-forming composition, a coating film including the silicon-containing polymer (A) as the main component can be formed. As is described below, by forming a coating film including the silicon-containing polymer (A) as the main component on surfaces of various articles to be treated, it is possible to provide the articles to be treated with metal supporting ability.
The silicon-containing polymer (A) is as described above. The silicon-containing polymer (A) content in the film-forming composition is not particularly limited and may be set depending on the desired film thickness. From the viewpoint of film-forming properties, the silicon-containing polymer (A) content in the film-forming composition is preferably 1% by mass or more and 50% by mass or less, more preferably 5% by mass or more and 40% by mass or less, and particularly preferably 10% by mass or more and 35% by mass or less.
The film-forming composition includes a solvent (S). The solvent (S) is not particularly limited, so long as the silicon-containing polymer (A) is soluble in it.
Suitable examples of the solvent (S) include alcohols such as methanol, ethanol, propanol, and n-butanol; polyhydric alcohols such as ethylene glycol, diethylene glycol, propylene glycol, and dipropylene glycol;
ketones such as acetone, methyl ethyl ketone, cyclohexanone, methyl-n-amyl ketone, methyl isoamyl ketone, and 2-heptanone; lactone-ring-containing organic solvents such as γ-butyrolactone;
polyhydric alcohol derivatives, including ester-bond-containing compounds such as ethylene glycol monoacetate, diethylene glycol monoacetate, propylene glycol monoacetate, and dipropylene glycol monoacetate, and ether-bond-containing compounds such as monoalkyl ethers, for example, monomethyl ether, monoethyl ether, monopropyl ether, and monobutyl ether, or monophenyl ethers of the above polyhydric alcohols or the above ester-bond-containing compounds, and the like; cyclic ethers such as dioxane and esters such as methyl lactate, ethyl lactate, methyl acetate, ethyl acetate, butyl acetate, methyl pyruvate, ethyl pyruvate, methyl methoxypropionate, and ethyl ethoxypropionate;
aromatic organic solvents such as anisole, ethyl benzyl ether, cresyl methyl ether, diphenyl ether, dibenzyl ether, phenetole, butyl phenyl ether, ethylbenzene, diethylbenzene, amylbenzene, isopropylbenzene, toluene, xylene, cymene, and mesitylene; and nitrogen-containing organic solvents such as N,N,N′,N′-tetramethylurea, N,N,2-trimethylpropionamide, N,N-dimethylacetamide, N,N-dimethylformamide, N,N-diethylacetamide, N,N-diethylformamide, 1,3-dimethyl-2-imidazolidinone, N-methylpyrrolidone, and N-ethylpyrrolidone. Two or more of these solvents may be used in combination.
Among these solvents, propylene glycol monomethyl ether acetate (PGMEA), propylene glycol monomethyl ether (PGME), N,N,N′,N′-tetramethylurea, and butanol are preferable.
It is also preferred that the solvent (S) include a cycloalkyl acetate represented by the following formula (S1). The film-forming composition includes a solvent (S) including a cycloalkyl acetate represented by the following formula (S1) together with the silicon-containing resin (A), thereby the coating film formed using the film-forming composition has good heat resistance.
(In the formula (S1), RS1 is an alkyl group having 1 or more and 3 or less carbon atoms, p is an integer of 1 or more and 6 or less, and q is an integer of 0 or more and (p+1) or less.).
Specific examples of the cycloalkyl acetate represented by the formula (S1) include cyclopropyl acetate, cyclobutyl acetate, cyclopentyl acetate, cyclohexyl acetate, cycloheptyl acetate, and cyclooctyl acetate. Among these, cyclohexyl acetate and cyclooctyl acetate are preferable because acquisition thereof is easy, and a coating film having excellent heat resistance can be easily formed. Two or more cycloalkyl acetates represented by the formula (S1) may be combined as the solvent (S).
The content of the cycloalkyl acetate represented by the formula (S1) in the solvent (S) is not particularly limited, so long as the object of the present invention is not defeated. The content of the cycloalkyl acetate represented by the formula (S1) in the solvent (S) is typically, for example, 30% by mass or more, preferably 50% by mass or more, more preferably 70% by mass or more, and particularly preferably 90% by mass or more, and it may be 100% by mass.
The amount of the solvent (S) to be used is not particularly limited, so long as the object of the present invention is not defeated. From the viewpoint of film-forming properties, the solvent (S) is used so that the solid content concentration in the film-forming composition is preferably 1% by mass or more and 50% by mass or less and more preferably 10% by mass or more and 40% by mass or less.
The film-forming composition may contain, in addition to the silicon-containing polymer (A) and the solvent (S), various components that are conventionally added to film-forming compositions used in various applications. Examples of other components include a photopolymerization initiator, an acid generator, a base generator, a catalyst, a silane coupling agent, an adhesion promoter, a dispersant, a surfactant, an ultraviolet absorber, an antioxidant, a defoaming agent, a viscosity modifier, a colorant, and the like. These components are blended, each in a typical amount, into the film-forming composition.
The method for producing the film-forming composition is not particularly limited. A typical method is to uniformly mix the components described above each in a predetermined amount and dissolve the solid matter in the solvent (S) to produce the film-forming composition. For removal of very small insoluble matter, the film-forming composition may be filtered through a filter with a desired pore size.
A method for supporting a metal compound on a surface of an object to be treated includes:
forming a coated film by applying the film-forming composition onto the surface of the object to be treated,
drying the coated film to obtain the coating film including the silicon-containing polymer (A), and
bringing the coating film into contact with a metal compound including an elemental metal. According to the method described above, by bringing a coating film mainly including the silicon-containing polymer (A) having a group represented by the formula (1) formed on the surface of an object to be treated into contact with a metal compound containing an elemental metal, the surface of the object to be treated can support the metal compound.
The method for forming a coated film on the surface of the object to be treated is not particularly limited. For example, the film-forming composition is applied by a method such as a spraying method, a spin coating method, a roll coating method, a dipping method, or a drip method to form a coated film on a substrate. The thickness of the coated film is not particularly limited. Typically, the coated film is formed in a thickness such that a coating film with a thickness of preferably 0.1 nm or more and 20 μm or less, more preferably 0.5 nm or more and 1000 nm or less, further preferably 0.5 nm or more and 500 nm or less, and particularly preferably 1 nm or more and 100 nm or less can be formed.
Objects to be treated include various substrates; porous materials for supporting catalytic compounds; housings for various devices; exterior materials for transportation vehicles such as automobiles, motorcycles, tricycles, railroad cars, ships, aircrafts, and helicopters; exterior materials for buildings; glass for buildings; mirrors; exhaust pipes for discharging exhaust gas generated by combustion from internal combustion engines, boilers, combustion furnaces for burning fossil fuels, and combustion furnaces for burning combustible wastes; various articles to be plated; substrates such as magnetic tapes, magnetic films, and magnetic sheets; optical materials such as lenses, high refractive index films, low refractive index films, prism sheets, and microlenses; ceramic capacitors, and multilayer ceramic capacitors; chemical apparatuses such as pipes, heat exchangers, storage tanks, reaction tanks, microreactors, and valves; LEDs; heat dissipation components such as heat sinks, and the like.
The material for the object to be treated is not particularly limited. Suitable examples of the material of the object to be treated include inorganic materials such as metal, silicon, and glass, polyester resins, polycarbonate resins, polyamide resins, polystyrene, polyethylene, polypropylene, acrylic resins, epoxy resins, polyarylene sulfide resins, polyimide resins, and polyamide-imide resins, and the like. The thickness of the substrate is not particularly limited, and the substrate may be a film or a sheet.
The coated film formed on the surface of the object to be treated in this manner is then dried. A method for drying the coated film includes air drying or a baking treatment in a temperature range of 60° C. or more and 150° C. or less. By the drying treatment, a coating film including the silicon-containing polymer (A) as a main component is formed.
The coating film is then brought into contact with a metal compound containing an elemental metal. A method for bringing the coating film into contact with the metal compound is not particularly limited. A preferred method is to contact a coating film with a solution of the metal compound, a liquid containing a colloid of the metal compound, or the like. The method for bringing the coating film into contact with a liquid containing the metal compound is not particularly limited. The method includes a method of applying a liquid containing the metal compound onto the coating film by a method similar to the method for forming the coated film, or a method of immersing an object to be treated having a coating film in a liquid containing the metal compound.
The concentration of the metal compound in the liquid containing the metal compound is not particularly limited as long as a desired amount of the metal compound can be supported on the surface of the object to be treated. For example, the concentration of the metal compound in the liquid containing the metal compound is preferably between 0.1% by mass or more and 30% by mass or less, more preferably 0.5% by mass or more and 20% by mass or less, and most preferably 1% by mass or more and 10% by mass or less.
The solvent or dispersant contained in the liquid containing the metal compound is not particularly limited as long as the metal compound is dissolved or dispersed in a colloidal form. The solvent or dispersant may be water, an organic solvent, or an aqueous solution of an organic solvent, and is preferably water. For the purpose of adjusting solubility and dispersibility of the metal compound, an acid such as hydrochloric acid, nitric acid, sulfuric acid, acetic acid, phosphoric acid, or the like, or a base such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, or the like may be added to the liquid in which the metal compound is contained.
The type of the metal compound is not particularly limited and is selected as appropriate according to the properties to be imparted to the surface of the object to be treated. Some examples of the relationship between the properties imparted to the surface of the object to be treated and the metal elements contained in the metal compound are given below.
Photodegradation of organic matter: Ti
Decomposition treatment of exhaust gas: Pt, V, Rh
Pre-treatment for plating or imparting conductivity: Pd, Ni, Cu, Ag, Au
Increase in refractive properties or increase in permittivity:
Imparting corrosion resistance: Ta
Imparting fluorescence: Zn
Imparting thermal conductivity: Al
The metal compound is not particularly limited to a metal compound that can be supported by the silicon-containing polymer (A). Examples of the metal compound include elemental metals, metal ions (salts such as carbonates, sulfates, phosphates, and halides (chlorides, bromides, etc.)), metal oxides, metal complex oxides, metal sulfides, and metal selenides. As for the complex oxide, it may contain metallic elements and semi-metallic elements such as Si, Ge, As, and Sb.
Preferred examples of the elemental metals contained in the metal compound include Na, Mg, Al, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Sr, Zr, Nb, Mo, Ru, Rh, Pd, Ag, Cd, In, Sn, Cs, Ba, Ta, W, Os, Ir, Pt, and Au.
Specific examples of the metal compound include titania (TiO2), strontium titanate (SrTiO3), zinc oxide (ZnO2), tin oxide (SnO2), cadmium selenide (CdSe), cadmium sulfide (CdS), tungsten oxide (WO3), potassium tantalate (KTaO3), silica (SiO2), tantalum oxide (Ta2O5), tantalum-based complex oxides (LiTaO3, NaTaO3, CaTa2O5, BaTa2O5, Sr2Ta2O5), niobium-based complex oxides (K4Nb5O17, Sr2Nb2O7, Cs2Nb4O11), zirconium oxide (ZrO2), gallium-based oxide (ZnGa2O4), indium-based complex oxides (CaIn2O4, SrIn2O4), germanium-based oxides (Zn4Ge2O4), antimony-based oxides (CaSb2O7, SrSb2O7), and vanadium-based oxides (V2O5). In addition, elemental metals, alloys, metal oxides, metal chlorides, metal carbonates, metal sulfates, and metal phosphates, including one or more elemental metals selected from the group consisting of Mg, Al, Ti, Cr, Mn, Fe, Co, Ni, Cu, Mo, Ru, Rh, Ag, W, Os, Ir, Pt, and Au, are also preferred as the metal compound.
After the coating film is contacted with a metal compound containing an elemental metal, the surface of the coating film may be cleaned with water or an organic solvent, if necessary. Through processes like these, a metal compound containing an elemental metal is supported on the surface of the object to be treated.
By the method described above, an article is produced which has a coating film which includes the aforementioned silicon-containing polymer and which supports a metal compound.
Among methods for producing the silicon-containing polymer, a method for producing polysilane in which one or more groups represented by the formula (1) are bonded to a silicon atom will be described below. The method for producing such polysilane includes homo-polymerization of a cyano group-containing halosilane compound represented by a following formula (1a) in the presence of metallic magnesium or copolymerization of the aforementioned cyano group-containing halosilane compound with a halosilane compound other than the aforementioned cyano group-containing halosilane compound in the presence of metallic magnesium.
The formula (1a) is represented by the following formula:
R2(2-p)X2Si—(R1—CN)p (1a).
In the formula (1a), X is a halogen atom, R1 is the same as R1 in the formula (1) above, R2 is a hydrocarbon group having 1 or more and 10 or less carbon atoms, and p is 1 or 2.
As the hydrocarbon group as R2, an alkyl group, an alkenyl group, a cycloalkyl group, a cycloalkenyl group, an aryl group, and an aralkyl group are preferable, and an alkyl group, an aryl group, and an aralkyl group are more preferable. When R2 is an alkyl group, an aryl group, or an aralkyl group, suitable examples of these groups are the same as the suitable examples when R in the formula (A1) is an alkyl group, an aryl group, or an aralkyl group.
As the halogen atom as X, chlorine and bromine are preferable, and chlorine is more preferable.
Suitable examples of cyano group-containing halosilane compounds represented by the formula (1a) include methyl(2-cyanoethyl)dichlorosilane, ethyl(2-cyanoethyl)dichlorosilane, n-propyl(2-cyanoethyl)dichlorosilane, isopropyl(2-cyanoethyl)dichlorosilane, phenyl(2-cyanoethyl)dichlorosilane, benzyl(2-cyanoethyl)dichlorosilane, methyl(3-cyano-n-propyl)dichlorosilane, ethyl(3-cyano-n-propyl)dichlorosilane, n-propyl(3-cyano-n-propyl)dichlorosilane, isopropyl(3-cyano-n-propyl)dichlorosilane, phenyl(3-cyano-n-propyl)dichlorosilane, benzyl(3-cyano-n-propyl)dichlorosilane, methyl(4-cyano-n-butyl)dichlorosilane, ethyl(4-cyano-n-butyl)dichlorosilane, n-propyl(4-cyano-n-butyl)dichlorosilane, isopropyl(4-cyano-n-butyl)dichlorosilane, phenyl(4-cyano-n-butyl)dichlorosilane, and benzyl(4-cyano-n-butyl)dichlorosilane.
The halosilane compound other than the cyano group-containing halosilane compound represented by the formula (1a) may be a dihalosilane compound, a trihalosilane compound, or a tetrahalosilane compound, and a dihalosilane compound is preferable. As a suitable example of the halosilane compound other than the cyano group-containing halosilane compound represented by the formula (1a), a dihalosilane compound represented by a following formula (2a) is preferable.
SiX2R22 (2a).
In the formula (2a), X and R2 are the same as X and R2 in the formula (1a). Suitable examples of the dihalosilane compound represented by the formula (2a) include dimethyldichlorosilane, diethyldichlorosilane, di-n-propyldichlorosilane, diisopropyldichlorosilane, methylethyldichlorosilane, methylphenyldichlorosilane, methylbenzyldichlorosilane, diphenyldichlorosilane, phenylbenzyldichlorosilane, and dibenzyldichlorosilane.
An amount of the cyano group-containing halosilane compound represented by the formula (1a) relative to the total amount of the halosilane compound used in the production of the polysilane is not particularly limited, and can be decided as appropriate by taking into account the amount of the group represented by the formula (1) in the polysilane.
Metallic magnesium can be any component as long as it contains magnesium in the form of active metallic magnesium that is not in the form of magnesium ions or the like. Typically, metallic magnesium (elemental magnesium), magnesium alloys, and the like are used. The type of magnesium alloy is not particularly limited. For example, a magnesium alloy containing magnesium and one or more components selected from aluminum, zinc, and rare earth elements (scandium, yttrium, etc.) is mentioned. A metallic magnesium component that includes metallic magnesium can be used alone or in combination of two or more types.
The shape of the metallic magnesium component is not particularly limited as long as the reaction of the halosilane compound is not impaired. The shape of the metallic magnesium component includes powdered granular (powder, granular, etc.), ribbon, flake, rod, plate, etc., and the powdered granular is preferred. The average particle diameter of the powdered granular metallic magnesium component is, for example, preferably 1 μm or more and 10000 μm or less, more preferably 10 μm or more and 7000 μm or less, more preferably 15 μm or more and 5000 μm or less, and most preferably 20 μm or more and 3000 μm or less.
In some cases, a coating film (such as an oxide coating film) is formed on the surface of a metallic magnesium component. Such a coating film may have an adverse effect on the reaction. Therefore, when a coating film is formed on the surface of a metallic magnesium component, it is preferable to use the metallic magnesium component after removing the coating film by cutting, hydrochloric acid cleaning, or other methods.
The amount of the metallic magnesium component used is preferably, for example, 0.3 equivalents or more and 30 equivalents or less in magnesium equivalent with respect to the halogen atom in the total amount of the halosilane compound, more preferably 0.5 equivalents or more and 20 equivalents or less, and most preferably 1 equivalent or more and 15 equivalents or less.
The polymerization reaction of the halosilane compound should be carried out in the presence of at least a metallic magnesium component. In order to promote the polymerization of the halosilane compound, it is preferable to carry out the polymerization of the halosilane compound in the presence of the metallic magnesium component and a lithium compound.
Examples of lithium compounds include lithium halides such as lithium chloride, lithium bromide, and lithium iodide, and lithium salts of inorganic acids such as lithium nitrate, lithium carbonate, lithium bicarbonate, lithium hydrochloride, lithium sulfate, lithium perchlorate, and lithium phosphate. As the lithium compound, lithium halide is preferable, and lithium chloride is more preferable. These lithium compounds may be used alone or in combination of two or more types thereof.
As the used amount of the lithium compound, 0.1 part by mass or more and 200 parts by mass or less is preferable, 1 part by mass or more and 150 parts by mass or less is more preferable, and 2 parts by mass or more and 100 parts by mass or less is most preferable, with respect to 100 parts by mass of the halosilane compound.
As reaction solvents, aprotic solvents are preferably used. Preferred examples of the aprotic solvents include ethers such as 1,4-dioxane, tetrahydrofuran, tetrahydropyran, diethyl ether, diisopropyl ether, 1,2-dimethoxyethane, and bis(2-methoxyethyl) ether; carbonates such as propylene carbonate; nitriles such as acetonitrile and benzonitrile; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfoxides such as dimethyl sulfoxide; aromatic hydrocarbons such as benzene, toluene, and xylene; and aliphatic hydrocarbons such as hexane, cyclohexane, octane, and cyclooctane. These aprotic solvents may be used alone or in combination of two or more types thereof.
Halosilanes react rapidly with water. For this reason, it is preferable to use a reaction vessel and materials used in the reaction after they have been sufficiently dried (dehydrated) beforehand.
The temperature at which polymerization of halosilane compound is carried out is not particularly limited as long as the polymerization reaction proceeds well. The polymerization temperature is usually preferably −20° C. or more and 150° C. or less, more preferably 0° C. or more and 100° C. or less, and most preferably 10° C. or more and 80° C. or less. The time of the polymerization reaction is adjusted according to the type of the halosilane compound, the metal halide, and the amount of the metallic magnesium component. For example, polymerization reaction time of 5 minutes or more is preferable, 30 minutes or more and 100 hours or less is more preferable, 1 hour or more and 80 hours or less is more preferable, and 2 hours or more and 60 hours or less is most preferable.
Below, the present will be described in more detail by reference to the Examples, but the present invention is not limited to these Examples.
In a round-bottom flask equipped with a three-way cock with an inner volume of 1000 ml, 43.45 g of granular magnesium (grain diameter 20 μm or more and 1000 μm or less), 5.26 g of tris(acetylacetonato)iron(III) as a catalyst, and 1.26 g of anhydrous lithium chloride were put. The atmosphere in the reactor was set to 50° C. and the pressure therein was reduced to 1 mmHg (=133 kPa) to dry the inside of the reactor (flask). After this, dry argon gas was introduced into the reactor, and 132.13 ml of tetrahydrofuran (THF) dried with sodium-benzophenone ketyl in advance was added to the reactor. Subsequently, the contents in the reactor were stirred at 25° C. for about 60 minutes. Next, 54.64 g (0.3 mol) of methyl(3-cyano-n-propyl)dichlorosilane purified by distillation in advance was added to this reactor by a syringe and the reaction mixture in the reactor was stirred at 25° C. for about 24 hours. After completion of the reaction, 1000 ml of 1 N (=1 mol/L) hydrochloric acid was put in the reaction mixture, and a formed silane polymer was then extracted by 500 ml of toluene. The toluene phase was washed with 200 ml of pure water ten times, and the toluene phase was then dried over anhydrous magnesium sulfate. Subsequently, toluene was distilled off from the toluene phase to give 18.2 g of a linear methyl(3-cyano-n-propyl)silane polymer (mass average molecular weight (Mw) 4200).
The methyl(3-cyano-n-propyl)silane polymer obtained in Example 1 was dissolved in cyclohexanol acetate so that the solid content concentration was 10% by mass to obtain a film-forming composition. On a silicon substrate (6 inches), the film-forming composition was spin-coated to form a coated film, and then the coated film was dried at 80° C. for 120 seconds to form a coating film with a thickness of 80 nm. The silicon substrate having the coating film was immersed in a PdCl2 hydrochloric acid-acidified aqueous solution containing 4% by mass of PdCl2, followed by immersion of the silicon substrate in ion-exchange distilled water for cleaning. The silicon substrate after cleaning was dried to obtain a silicon substrate having a coating film that supports PdCl2. Analyzing the surface of the silicon substrate obtained and the surface of the untreated silicon substrate by XPS (X-ray photoelectron spectroscopy), a peak originating from PdCl2 was observed for the silicon substrate obtained in Example 2, while no peak originating from PdCl2 was observed on the surface of the untreated silicon substrate.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2019-093797 | May 2019 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2020/018336 | 4/30/2020 | WO | 00 |
