JP5880094B2 - Metal pattern forming method and metal pattern - Google Patents

Description

The present invention relates to a metallic pattern forming method and a metal pattern.

  As a method for forming a metal pattern such as a wiring pattern or an electrode pattern on a circuit board, a method using a photolithography technique is known. In this method, a homogeneous metal film is first formed on a substrate. As a method for forming the metal film, it is possible to use a vapor deposition method or a sputtering method in addition to the plating method. Then, a resist solution is applied on the formed metal film to form a resist layer. Next, the resist layer is patterned by irradiating the resist layer with ultraviolet rays using a photomask and then developing the resist layer. Next, the metal film not covered with the resist layer is removed by etching, and the remaining resist portion is peeled off to obtain a metal pattern. The method using the photolithography technique makes it possible to make the line width of the wiring pattern to be formed on the order of submicrons, which is an effective method for forming a metal film.

However, in a plating method used for forming a metal film, formation of a seed layer by a sputtering method and a plating process are usually required. Since sputtering needs to be performed in a vacuum, there are significant restrictions on the apparatus and operation. Also, the process takes a long time and the production efficiency is low. In the plating process, the waste liquid treatment of the plating solution is a big environmental problem.
Similarly, even when vapor deposition or sputtering is used to form a metal film, it is necessary to form the metal film in a vacuum, so there are significant restrictions on the equipment and operation, and the processing takes a long time and efficiency. A metal film cannot be formed well. In any of the methods, there is a problem that unnecessary metal films need to be removed, and therefore, there is a lot of waste from the viewpoint of the use efficiency of raw materials, and the manufacturing cost of the circuit board increases.

Therefore, in recent years, a metal pattern forming method in which a metal pattern is directly drawn using an application method such as an ink jet method or a screen printing method has attracted attention.
Patent Document 1 proposes a method for forming a silver film or a silver image using a composition containing silver oxide and a reducing agent such as glycerin. Patent Document 2 proposes a method of forming a metal pattern using an ink-like composition containing a metal salt such as gold, silver or copper and a reducing agent such as glycerin.

  However, in the case of the coating method using the composition as described above, the fluidity of the ink-like composition after coating is too high, so-called bleeding or flow-out phenomenon occurs, and a pattern having a desired shape is accurately formed. There was a problem that it could not be formed. Further, there is a problem that only a thin metal pattern can be formed.

  If a composition containing metal particles or the like is used instead of a metal salt or the like, it is possible to form a metal pattern having a certain thickness. However, if metal particles having a large particle diameter are used to form a metal pattern having a larger film thickness, the metal pattern can be formed by a self-supporting metal film due to insufficient adhesion between the metal particles. It could be difficult. In particular, when metal particles such as copper having a high ionization tendency are used, it is more difficult to form a self-supporting metal film because the metal oxide usually formed on the particle surface is difficult to be reduced. It was.

JP 2004-176079 A JP 2008-205430 A

  The present invention has been made based on the above findings. That is, an object of the present invention is to provide a pattern forming method capable of easily forming a pattern. And it is providing the metal pattern formation method which can be efficiently formed with the desired film thickness and shape even if it is a metal pattern which consists of a metal with a large ionization tendency using the pattern formation method.

  Another object of the present invention is to provide a metal pattern which can be formed with a desired film thickness and shape by the above-described metal pattern forming method and can be constituted by a metal having a high ionization tendency.

  Other objects and advantages of the present invention will become apparent from the following description.

The first aspect of the present invention is:
[1] A step of forming a coating film of a first composition containing a polymer having a polyacetal structure on a substrate, and forming a resin layer on the substrate;
[2] It relates to a pattern forming method comprising a step of locally heating to remove the resin layer into an arbitrary shape.

  In the first aspect of the present invention, the local heating in the step [2] is preferably performed by irradiation with radiation.

  In the first embodiment of the present invention, the polymer contained in the first composition preferably has a repeating unit represented by the following formula (α).

（上記式（α）中、Ｘ^１およびＸ^２はそれぞれ独立して水素原子、ハロゲン原子、炭素数１〜２０の炭化水素基からなる群から選択される１以上の原子または置換基を表す。Ｘ^３およびＸ^４は互いに連結して１以上の環を形成する、合計炭素数が１〜１５の原子団を表す。ここで、各炭化水素基およびその原子団上の水素原子はそれぞれ独立に、ハロゲン原子および炭素数１〜１０のアルコキシ基からなる群から選択される原子または置換基によって置換されていてもよい。）

(In the formula (α), X ¹ and X ² each independently represent one or more atoms or substituents selected from the group consisting of a hydrogen atom, a halogen atom, and a hydrocarbon group having 1 to 20 carbon atoms. X ³ and X ⁴ represent an atomic group having a total carbon number of 1 to 15 which is linked to each other to form one or more rings, wherein each hydrocarbon group and the hydrogen atom on the atomic group are independently And may be substituted with an atom or a substituent selected from the group consisting of a halogen atom and an alkoxy group having 1 to 10 carbon atoms.)

  In the first aspect of the present invention, the polymer contained in the first composition preferably has a repeating unit represented by the following formula (β).

（上記式（β）中、Ｒ^１はハロゲン原子、ヒドロキシル基、炭素数１〜２０の炭化水素基および炭素数１〜４のアルコキシ基からなる群から選択される１以上の原子または置換基を表し、ｍは０〜４の整数を表し、ｎは５〜１０００の整数を表す。ここで、ｎはその繰り返し単位の繰り返し数を表す。ｍが２以上の場合、Ｒ^１は互いに同一であってもよく、また異なっていてもよい。）

(In the above formula (β), R ¹ represents one or more atoms or substituents selected from the group consisting of a halogen atom, a hydroxyl group, a hydrocarbon group having 1 to 20 carbon atoms and an alkoxy group having 1 to 4 carbon atoms. M represents an integer of 0 to 4, and n represents an integer of 5 to 1000. Here, n represents the number of repetitions of the repeating unit, and when m is 2 or more, R ^{1 s} are identical to each other. May be different or different.)

  In the first aspect of the present invention, the polymer contained in the first composition preferably has a terminal structure represented by the following formula (γ).

（上記式（γ）中、Ｚは水素原子、炭素数１〜２０の炭化水素基、炭素数１〜１０のアルコキシ基、アシル基、カルボニル基、エステル基およびホルミル基、アミノ基、アルキルアミノ基、アリールアミノ基、イソシアネート基、アミド基、ニトロ基およびシアノ基、並びに窒素原子、酸素原子または硫黄原子を含む複素環式基からなる群から選択される置換基を表す。ここで、炭化水素基、アルコキシ基、アシル基、エステル基、アルキルアミノ基、アリールアミノ基、アミド基、複素環式基上の水素原子はハロゲン原子、ヒドロキシル基、カルボニル基、炭素数１〜２０の炭化水素基および炭素数１〜１０のアルコキシ基からなる群から選択される１種以上により置換されていてもよい。）

(In the above formula (γ), Z is a hydrogen atom, a hydrocarbon group having 1 to 20 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, an acyl group, a carbonyl group, an ester group and a formyl group, an amino group, and an alkylamino group. And a substituent selected from the group consisting of an arylamino group, an isocyanate group, an amide group, a nitro group and a cyano group, and a heterocyclic group containing a nitrogen atom, an oxygen atom or a sulfur atom, wherein the hydrocarbon group , An alkoxy group, an acyl group, an ester group, an alkylamino group, an arylamino group, an amide group, and a heterocyclic group include a halogen atom, a hydroxyl group, a carbonyl group, a hydrocarbon group having 1 to 20 carbon atoms, and a carbon atom. (It may be substituted with one or more selected from the group consisting of alkoxy groups of 1 to 10).

A second aspect of the present invention is a metal pattern forming method using the pattern forming method of the first aspect of the present invention,
[3] Oxide whose portion including the surface portion is a metal oxide in the removed portion of the resin layer obtained by removing the resin layer in an arbitrary shape in the step [2] of the pattern forming method of the first aspect of the present invention And at least one metal oxide-containing particle selected from metal-metal oxide composite particles (A1) and metal oxide particles (A2) other than a part including the surface portion thereof. Filling a second composition containing A);
[4] A method of forming a metal pattern, comprising: heating, heating the second composition filled in the removal portion, and removing the resin layer.

  In the second aspect of the present invention, the second composition preferably further contains alditol (B) and an alditol oxide (C).

  In the second embodiment of the present invention, the alditol oxide (C) is preferably an alditol (B) oxide.

  In the second aspect of the present invention, the alditol (B) is preferably glycerin.

  2nd aspect of this invention WHEREIN: As for 2nd composition, content of the oxide (C) of alditol is 1 mass part-50 mass parts with respect to 100 mass parts of alditol (B). preferable.

  In the second aspect of the present invention, it is preferable to use an ink jet method for filling the removed portion in the step [3] with the second composition.

  2nd aspect of this invention WHEREIN: It is preferable that the temperature of the heating of process [4] is 100 to 300 degreeC.

  According to a third aspect of the present invention, there is provided a metal pattern formed using the metal pattern forming method according to the second aspect of the present invention.

  According to the first aspect of the present invention, a pattern forming method capable of easily forming a pattern is provided.

  According to the 2nd aspect of this invention, even if it is a metal pattern which consists of a metal with a big ionization tendency, the metal pattern formation method which can be efficiently formed with a desired film thickness and shape is provided.

  According to the third aspect of the present invention, there is provided a metal pattern that can be formed with a desired film thickness and shape and can be configured with a metal having a high ionization tendency.

(A)-(d) is process drawing explaining the pattern formation method and metal pattern formation method of embodiment of this invention.

  Hereinafter, embodiments of the present invention will be described with reference to the drawings as appropriate.

  FIG. 1A to FIG. 1D are process diagrams illustrating a pattern forming method and a metal pattern forming method according to an embodiment of the present invention.

  It is preferable that the metal pattern formation method of embodiment of this invention is comprised including the process of implementing the pattern formation method of embodiment of this invention. And the metal pattern formation method of embodiment of this invention has at least each process of process [1]-process [4] shown by Fig.1 (a)-FIG.1 (d) in this order. .

  At this time, in the steps [1] and [2] shown in FIG. 1A and FIG. 1B, the resin layer 2 is provided on the substrate 1, and a part of the resin layer 2 is locally heated. This is a pattern forming step of removing and forming a pattern made of resin. That is, this is a step of performing the pattern forming method of the present embodiment. The subsequent steps [3] and [4] shown in FIG. 1 (c) and FIG. 1 (d) are applied to the removal portion 3 of the resin layer 2 of the pattern formed in the steps [1] and [2]. This is a metal pattern forming step in which a metal pattern 5 is formed by filling a composition for forming a pattern made of metal (second composition 4) and heating.

  Therefore, the metal pattern forming method of the embodiment of the present invention implements the pattern forming method of the present embodiment for forming a resin pattern, and uses the pattern formed there and the composition for forming the metal pattern. , Forming a metal pattern.

  Specifically, in the pattern forming method of the present embodiment, [1] a coating film of a first composition containing a polymer having a polyacetal structure is formed on a substrate 1 as shown in FIG. 1 has a step of forming the resin layer 2 on the substrate 1 (hereinafter also referred to as a resin layer forming step).

  Thereafter, in the pattern forming method of the present embodiment, [2] local heating is performed to remove the resin layer 2 into an arbitrary shape as shown in FIG. The process (henceforth a removal part formation process) is formed.

  That is, the pattern forming method according to the present embodiment includes the step [1] and the step [2] shown in FIGS. 1A and 1B, and forms the removal portion 3 in the resin layer 2. Thus, a pattern having a desired shape made of a resin can be easily formed. And the pattern formation method of this embodiment can comprise the metal pattern formation method of this embodiment by combining with the process mentioned later.

  Then, the metal pattern forming method of the present embodiment uses the pattern forming method of the present embodiment, and after step [1] and step [2] of performing the pattern forming method of this embodiment, FIG. [3] process shown and [4] process shown by FIG.1 (d) are comprised.

  That is, in the metal pattern forming method of this embodiment, the part including the surface part is made of a metal oxide in the removed part 3 formed in [3] step [2], and the part other than the part including the surface part is included. Filled with the second composition 4 containing at least one metal oxide-containing particle (A) selected from metal-metal oxide composite particles (A1) and metal oxide particles (A2) comprising the metal Step (hereinafter also referred to as a composition filling step).

  Thereafter, in the metal pattern forming method of the present embodiment, [4] heating shown in FIG. 1 (d) is performed to heat the second composition 4 filled in the removing unit 3 and to form the resin layer 2. It has the process (henceforth a heating process) which removes and forms the metal pattern 5 which consists of metals.

  As described above, the metal pattern forming method of the present embodiment includes the steps [1] to [4], and the pattern forming method of the present embodiment is performed in the steps [1] and [2]. After forming a pattern made of resin, formation of a metal pattern made of metal is realized using the pattern.

  Hereinafter, with respect to the pattern forming method of the present embodiment and the metal pattern forming method of the present embodiment, [1] step (resin layer forming step), [2] step (removal part forming step), [3] step (composition filling) Steps) and [4] Steps (heating step) will be described in more detail.

<Resin layer forming step>
In the resin layer forming step, a coating film of the first composition containing a polymer having a polyacetal structure is formed on a substrate, and a resin layer is formed on the substrate. The thickness of the resin layer is preferably 1 μm to 1000 μm.

  The first composition of the present embodiment can easily form a resin layer on the surface of an object such as a substrate by coating at a normal temperature, for example, around 25 ° C. The obtained resin layer can be decomposed and removed from the substrate by low-temperature heat treatment.

As the substrate, a substrate having heat resistance and chemical resistance that can withstand the formation of a resin pattern and a metal pattern is required. Examples of such a substrate include metal substrates such as a copper plate, an iron plate, and an aluminum plate. In addition, an inorganic substrate such as a silicon substrate, a glass substrate such as soda glass, borosilicate glass, silica glass, or quartz glass, or a ceramic substrate such as alumina can be given. Moreover, organic substrates, such as a polyimide substrate, a polyamide substrate, a polyquinoxaline substrate, can be mentioned.
Next, the 1st composition of this embodiment containing the polymer which has the above-mentioned polyacetal structure is demonstrated.

[First composition containing a polymer having a polyacetal structure]
The polymer having a polyacetal structure contained in the first composition of the present embodiment can be represented by the following formula (α).
The first composition of the present embodiment can contain an α-methylstyrene polymer, a (meth) acrylate / α-methylstyrene copolymer, etc., instead of the polymer having a polyacetal structure. However, in this embodiment, the use of a polymer having a polyacetal structure is particularly preferable.

（上記式（α）中、Ｘ^１およびＸ^２はそれぞれ独立して水素原子、ハロゲン原子、炭素数１〜２０の炭化水素基からなる群から選択される１以上の原子または置換基を表す。Ｘ^３およびＸ^４は互いに連結して１以上の環を形成する、合計炭素数が１〜１５の原子団を表す。ここで、各炭化水素基および原子団上の水素原子はそれぞれ独立に、ハロゲン原子および炭素数１〜１０のアルコキシ基からなる群から選択される原子または置換基によって置換されていてもよい。）

(In the formula (α), X ¹ and X ² each independently represent one or more atoms or substituents selected from the group consisting of a hydrogen atom, a halogen atom, and a hydrocarbon group having 1 to 20 carbon atoms. X ³ and X ⁴ represent an atomic group having a total carbon number of 1 to 15 which is linked to each other to form one or more rings, wherein each hydrocarbon group and a hydrogen atom on the atomic group are each independently (It may be substituted with an atom or a substituent selected from the group consisting of a halogen atom and an alkoxy group having 1 to 10 carbon atoms.)

In the polymer having a polyacetal structure represented by the above formula (α), X ¹ and X ² are particularly preferably a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms (in the present specification, a hydrocarbon group) Is a concept including a linear or branched alkyl group, a cycloalkyl group or an aryl group unless otherwise specified.)

In the polymer having a polyacetal structure represented by the above formula (α), the atomic group having 1 to 15 carbon atoms composed of X ³ and X ⁴ includes an ethylene group (in this case) in addition to a methylene group. , One oxygen atom on the polymer chain and two adjacent carbon atoms and the ethylene group constitute a five-membered ring.), An alkylene group such as a propylene group or a butylene group, a cycloalkylene group, a cycloalkenylene Group, cycloalkadienyl group, arylene group and the like. From the viewpoints of polymer availability, stability, decomposition temperature, and the like, a cycloalkylene group, a cycloalkenylene group, a cycloalkadienyl group, an arylene group, and the like are preferable, and an arylene group is more preferable. Particularly preferably, polyphthalaldehyde represented by the following formula (β) is selected.

（上記式（β）中、Ｒ^１はハロゲン原子、ヒドロキシル基、炭素数１〜２０の炭化水素基および炭素数１〜４のアルコキシ基からなる群から選択される１以上の原子または置換基を表し、ｍは０〜４の整数を表し、ｎは５〜１０００の整数を表す。ここで、ｎは前記繰り返し単位の繰り返し数を表す。ｍが２以上の場合、Ｒ^１は互いに同一であってもよく、また異なっていてもよい。）

(In the above formula (β), R ¹ represents one or more atoms or substituents selected from the group consisting of a halogen atom, a hydroxyl group, a hydrocarbon group having 1 to 20 carbon atoms and an alkoxy group having 1 to 4 carbon atoms. M represents an integer of 0 to 4, and n represents an integer of 5 to 1000. Here, n represents the number of repetitions of the repeating unit, and when m is 2 or more, R ¹ are the same as each other. May be different or different.)

  When a polymer having a polyacetal structure is selected, it is preferable to apply a so-called end cap treatment to the end in order to prevent depolymerization. The terminal structure is not particularly limited as long as it can cap the —OH group. For example, a structure represented by the following formula (γ) can be selected.

（上記式（γ）中、Ｚは水素原子、炭素数１〜２０の炭化水素基、炭素数１〜１０のアルコキシ基、アシル基、カルボニル基、エステル基およびホルミル基、アミノ基、アルキルアミノ基、アリールアミノ基、イソシアネート基、アミド基、ニトロ基およびシアノ基、並びに窒素原子、酸素原子または硫黄原子を含む複素環式基からなる群から選択される置換基を表す。ここで、炭化水素基、アルコキシ基、アシル基、エステル基、アルキルアミノ基、アリールアミノ基、アミド基、複素環式基上の水素原子はハロゲン原子、ヒドロキシル基、カルボニル基、炭素数１〜２０の炭化水素基および炭素数１〜１０のアルコキシ基からなる群から選択される１種以上により置換されていてもよい。）

(In the above formula (γ), Z is a hydrogen atom, a hydrocarbon group having 1 to 20 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, an acyl group, a carbonyl group, an ester group and a formyl group, an amino group, and an alkylamino group. And a substituent selected from the group consisting of an arylamino group, an isocyanate group, an amide group, a nitro group and a cyano group, and a heterocyclic group containing a nitrogen atom, an oxygen atom or a sulfur atom, wherein the hydrocarbon group , An alkoxy group, an acyl group, an ester group, an alkylamino group, an arylamino group, an amide group, and a heterocyclic group include a halogen atom, a hydroxyl group, a carbonyl group, a hydrocarbon group having 1 to 20 carbon atoms, and a carbon atom. (It may be substituted with one or more selected from the group consisting of alkoxy groups of 1 to 10).

  In the structure represented by the above formula (γ), it is preferable that Z is a hydrocarbon group, an alkylamino group, an arylamino group, or a heterocyclic group, and particularly a hydrocarbon group, an alkylamino group, or an arylamino group. preferable.

  The molecular weight of the polymer having a polyacetal structure contained in the first composition is not particularly limited as long as it is suitable for the formation of the resin layer and the removal layer described above, but from the viewpoint of film forming properties and handling properties. The weight average molecular weight is preferably in the range of 1000 to 100,000. When the weight average molecular weight exceeds 100,000, the handling load may increase as the viscosity increases. The weight average molecular weight of the polymer can be determined by a gel permeation chromatography (GPC) method using standard polystyrene having a known molecular weight as a standard sample.

  The first composition may contain a low molecular weight compound that is solid at the decomposition start temperature of the polymer having a polyacetal structure (hereinafter sometimes simply referred to as “solid compound”). By blending such a solid compound, it is possible to take a shape in which the low molecular weight solid compound enters into the voids in the film generated with the network of high molecular weight polymers, thereby forming a dense film. It becomes possible.

  Examples of such solid compounds include benzoic acid and its derivatives such as benzoic acid, methyl benzoate, benzoin, gallic acid, methyl gallate, ethyl gallate, and propyl gallate; phthalic acid, phthalic anhydride, isophthalate Phthalates such as acid, terephthalic acid, phthalimide, N-hydroxyphthalimide and derivatives thereof; nicotinic acid and derivatives thereof such as nicotinic acid, nicotinamide, and isonicotinic acid; adamantane, 1,3-adamantanediol, 1,3 , 5-adamantanetriol, 1,3-adamantanediacetic acid, 2-adamantanol, 1-adamantanol, 2-adamantanone, 2-methyl-2-adamantanol, 1-adamantanecarboxylic acid and the like, and derivatives thereof; Camper such as camphor, borneol And derivatives thereof; include; anthracene, anthraquinone, hydroxy anthraquinone, anthracene and its derivatives such as amino anthraquinone.

  The first composition may further contain an organic solvent. The organic solvent is not particularly limited, and for example, alcohol solvents, ketone solvents, hydrocarbon solvents, ether solvents, other polar solvents, halogen solvents, and the like can be used.

  Examples of the alcohol solvent include alcohol solvents having one hydroxyl group such as methanol, ethanol, n-propanol, i-propanol, n-butanol, i-butanol, sec-butanol, and t-butanol; ethylene glycol, 1 , 2-propylene glycol, 1,3-butylene glycol, 2,4-pentanediol, 2-methyl-2,4-pentanediol, 2,5-hexanediol, 2,4-heptanediol, 2-ethyl-1 Polyhydric alcohol solvents having two or more hydroxyl groups such as 1,3-hexanediol, diethylene glycol, dipropylene glycol, triethylene glycol, tripropylene glycol; ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol Monopropyl ether, and ethylene glycol monobutyl ether, polyhydric alcohol partial ether-based solvent an alcohol having two or more hydroxyl groups formed by partially etherified are exemplified.

  Examples of the ketone solvent include acetone, methyl ethyl ketone, methyl-n-propyl ketone, methyl-n-butyl ketone, diethyl ketone, methyl-i-butyl ketone, methyl-n-pentyl ketone, ethyl-n-butyl ketone, and methyl-n-. Such as hexyl ketone, di-i-butyl ketone, trimethylnonanone, cyclopentanone, cyclohexanone, cycloheptanone, cyclooctanone, 2-hexanone, methylcyclohexanone, 2,4-pentanedione, acetonylacetone, diacetone alcohol, etc. Ketone solvents are exemplified.

  As the hydrocarbon solvent, n-pentane, cyclopentane, n-hexane, cyclohexane, n-heptane, cycloheptane, n-octane, cyclooctane, decane, cyclodecane, dicyclopentadiene hydride, benzene, toluene, xylene , Butylbenzene, t-butylbenzene, t-butylxylene, dodecylbenzene, durene, indene, tetrahydronaphthalene, decahydronaphthalene, squalane and the like.

  Examples of the ether solvent include diethyl ether, dipropyl ether, dibutyl ether, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol methyl ethyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol methyl ethyl ether, tetrahydrofuran, tetrahydropyran, bis ( 2-methoxyethyl) ether, p-dioxane, anisole, 2-methylanisole, 3-methylanisole, 4-methylanisole, fentol, 2-methylfentol, 3-methylfentol, 4-methylfentol, veratrol , 2-ethoxyanisole, 1,4-dimethoxybenzene and the like.

Examples of the halogen solvent include methylene chloride and chloroform.
These organic solvents can be used individually by 1 type or in mixture of 2 or more types.

  Although the polymer density | concentration which has a polyacetal structure in a 1st composition is not specifically limited, Preferably it is 0.1 mass%-50 mass%, More preferably, it is 1 mass%-20 mass%.

  The preparation method of the 1st composition containing the polymer which has a polyacetal structure is not specifically limited. For example, the solvent may be removed from the desired polymer obtained by cationic polymerization, anionic polymerization, radical polymerization, ring-opening polymerization, coordination polymerization, or condensation polymerization, and dissolved in a desired solvent separately. Polymerization may be performed in this, and this may be used as it is or after filtration.

  In addition, the first composition can contain an additive. For example, a surfactant (leveling agent), a wettability improver, an antifoaming agent, and the like may be included. Furthermore, a decomposition accelerator for accelerating the decomposition of the polymer may be included.

The surfactant is not particularly limited, but examples thereof include polyoxyethylene alkyl ethers such as polyoxyethylene lauryl ether, polyoxyethylene stearyl ether, polyoxyethylene cetyl ether, polyoxyethylene olein ether, and polyoxyethylene octylphenol. Polyoxyethylene alkyl allyl ethers such as ether, polyoxyethylene nonylphenol ether, polyoxyethylene polyoxypropylene block copolymers, sorbitan fatty acid esters such as sorbitan monolaurate, sorbitan monopalmitate, sorbitan monostearate, polyoxy Ethylene sorbitan monolaurate, polyoxyethylene sorbitan monopalmitate, polyoxyethylene sorbitan monostearate Nonionic leveling agents / surfactants of polyoxyethylene sorbitan fatty acid esters such as rate, polyoxyethylene sorbitan trioleate, polyoxyethylene sorbitan tristearate, Ftop (registered trademark) EF301, EF303, EF352 (Tochem Products) ), Megafuck (registered trademark) F171, F172, F173 (DIC), Florard FC430, FC431 (Sumitomo 3M), Asahi Guard (registered trademark) AG710, Surflon (registered trademark) S-381, S-382, SC101 SC102, SC103, SC104, SC105, SC106, Surfinol E1004, KH-10, KH-20, KH-30, KH-40 (Asahi Glass Co., Ltd.), Footent (registered trademark) 250, 251, Fluorine leveling agents and surfactants such as 22F and FTX-218 (Neos), organosiloxane polymers KP341, X-70-092, X-70-093 (Shin-Etsu Chemical Co., Ltd.), SH8400 (Toray Dow Corning) ), Acrylic acid-based or methacrylic acid-based polyflow No. 75, no. 77, no. 90, no. 95 (Kyoeisha Yushi Chemical Co., Ltd.).
These surfactants can be used alone or in combination of two or more.

  Of these, fluorine leveling agents and surfactants are particularly preferable as the surfactant. The compounding amount of the surfactant (leveling agent) is usually preferably 50 ppm to 1000 ppm, more preferably 70 ppm to 800 ppm in the first composition. When it is less than 50 ppm, the uniform coating property on the substrate is deteriorated, and when it exceeds 1000 ppm, the adhesion of the coating film is lowered.

  Examples of the decomposition accelerator include peracids such as performic acid or derivatives thereof, and quinone compounds such as hydroquinone. Of these, quinone compounds are preferred.

  The first composition comprising the above components has, as a main component, a weight reduction rate of 10% after 30 minutes at 100 ° C. when thermogravimetric analysis is performed in a nitrogen atmosphere. And (b) a polymer having a polyacetal structure in which the weight loss rate after 20 minutes from the start of measurement is 80% or more when the temperature is raised from 25 ° C. at 10 ° C./min. In the first composition, such a polymer is dissolved in an organic solvent as described above to form a solution, which is applied to the surface of the substrate that is the object to be protected and used to form a coating film. Then, a resin layer is formed on the surface of the substrate by removing the organic solvent from the coating film. At this time, for example, the removal of the organic solvent may be promoted by heating to about 100 ° C. or placing the object on which the liquid film is formed under reduced pressure. For heating, an appropriate heating device such as a hot plate or an oven can be used. Since the polymer having a polyacetal structure contained in the first composition has a weight reduction rate of 10% or less after 30 minutes at 100 ° C., the coating film formed on the substrate is free of solvent, etc. It is stable even when heated to about 100 ° C. in the process.

  In addition, as a method of forming the coating film of the first composition on the substrate, a known coating method can be used. Examples of the coating method include a spray method, a roll coating method, a spin coating method (sometimes referred to as a spin coating method or a spinner method), a slit coating method (slit die coating method), a bar coating method, and an inkjet coating method. A known method such as a method can be employed. Among these, the spin coating method or the slit coating method is preferable from the viewpoint that a coating film having a uniform thickness can be formed.

  The resin layer formed from the first composition can be completely removed from the substrate by heating at 100 ° C. to 300 ° C. That is, the resin layer formed from the first composition can be completely removed from the substrate even by heating at 200 ° C. or lower. The resin layer formed from the first composition becomes a resin layer suitable for the pattern forming method of the present embodiment, and by extension, the metal pattern forming method of the present embodiment.

<Removal part formation process>
In the removal portion forming step, the resin layer formed on the substrate in the resin layer forming step is locally heated to remove the resin layer into an arbitrary shape. And the removal part which penetrates the resin layer in the resin layer is formed.

  It is preferable that the above-mentioned local heating of the resin layer is performed by irradiation with radiation. That is, it is preferable that the resin layer formed on the substrate is irradiated with radiation to achieve local heating and the resin layer is removed. Radiation is a concept including visible light, ultraviolet light, far ultraviolet light, X-rays, charged particle beams, and the like.

  In particular, it is preferable to use laser light as radiation. Therefore, it is preferable to remove the resin layer by irradiating the resin layer formed on the substrate in the above-described resin layer forming step with laser light.

It is preferable to use YAG laser light as the laser light.
That is, the resin layer is irradiated with YAG laser light in an irradiation pattern corresponding to a desired metal pattern. As a result, local heating is performed in the irradiated portion, and the resin layer in the irradiated portion is removed. Then, as an opening pattern having a shape complementary to a desired metal pattern, a removal portion is formed in the resin layer to form a pattern made of resin. In this removal portion forming step, for example, laser light such as YAG laser light is used to form the removal portion, and the removal portion having a delicate shape with a narrow line width can be formed.

  As described above, the resin layer forming step and the removal portion forming step constitute the pattern forming method of the present embodiment, and can easily form a pattern made of a resin having a desired shape. And the removal part in the resin layer of the pattern which consists of resin formed by the resin layer formation process and the removal part formation process can be used in order to form a metal pattern in each process mentioned later. The resin layer forming step and the removal portion forming step can constitute a part of the metal pattern forming method of the present embodiment.

<Composition filling process>
In the composition filling step of the metal pattern forming method of the present embodiment, the second composition of the present embodiment is filled into the removed portion of the resin layer in the pattern formed in the removal portion forming step described above.
As a filling method, an inkjet method is preferably used. That is, the second composition is ejected by an ink jet method toward the removal portion penetrating the resin layer formed in the resin layer, and the second composition is filled in the removal portion.

Since the second composition is filled in the removed portion formed in the resin layer, there is no fear of bleeding or flowing out even when the fluidity of the second composition is high. The thickness of the composition can be increased within the range up to the thickness of the resin layer.
Next, the second composition will be described.

[Second composition]
The second composition of the present embodiment used in the metal pattern forming method of the present embodiment is a metal in which a part including the surface part is made of a metal oxide and a part other than the part including the surface part is made of the metal. It contains at least one metal oxide-containing particle (A) selected from metal oxide composite particles (A1) and metal oxide particles (A2). The second composition preferably further contains alditol (B) and an alditol oxide (C).

[Metal oxide-containing particles (A)]
A metal oxide containing particle (A) is a substance which supplies the metal which comprises the metal pattern of this embodiment formed using a 2nd composition. That is, when the second composition is used, a metal pattern made of a metal contained in the metal oxide-containing particles (A) is formed. For example, when a pattern made of copper is formed, copper oxide-containing particles are used as the metal oxide-containing particles (A).

  The metal oxide-containing particles (A) are at least one selected from metal-metal oxide composite particles (A1) (hereinafter also referred to as composite particles (A1)) and metal oxide particles (A2). That is, the metal oxide-containing particles (A) may be only the composite particles (A1) or only the metal oxide particles (A2), and the composite particles (A1) and the metal oxide particles (A2). ) And both. When the metal oxide-containing particles (A) include both the composite particles (A1) and the metal oxide particles (A2), the respective metals contained in the composite particles (A1) and the metal oxide particles (A2) are Usually the same type of metal.

  For example, when a pattern made of copper is formed as the metal pattern, the metal-metal oxide composite particles (A1) are copper-copper oxide composite particles, and the metal oxide particles (A2) are copper oxide particles. .

  In the metal oxide-containing particles (A), the metal oxide contained therein is reduced to alditol (B), which will be described later, contained in the second composition, converted into a metal, and bonded to each other. Thereby, a metal pattern is formed as a metal film.

[Metal-metal oxide composite particles (A1)]
The metal-metal oxide composite particles (A1) (also simply referred to as composite particles (A1) as described above) are composed of a metal oxide in a part including the surface part, and other than the part including the surface part. Part is a particle made of the metal. For example, in the case of copper-copper oxide composite particles, a part including the surface part is made of copper oxide, and the other part is made of copper. The part including the surface part means a part where the surface forms at least a part of the surface of the composite particle (A1). The portions other than the portion including the surface portion are made of the metal. Therefore, in the composite particle (A1), a portion made of a metal oxide is not included in a state where it does not appear on the surface of the composite particle (A1).

  The composite particles (A1) may be particles (composite particles (A1-1)) in which the entire surface portion is made of a metal oxide, or particles (composite particles) in which only a part of the surface portion is made of a metal oxide. Particle (A1-2)).

  The composite particle (A1-1) is a particle having a core part made of metal and an outer shell part containing the metal oxide that covers the entire core part. The surface of commercially available metal particles is usually oxidized to form a metal oxide film. This metal oxide film corresponds to the aforementioned outer shell. Therefore, commercially available metal particles usually correspond to metal-metal oxide composite particles (A1-1).

  The 50% by mass average particle diameter (D50) of the composite particles (A1) is preferably 0.1 μm to 10 μm, more preferably 0.1 μm to 5 μm, and still more preferably 0.1 μm to 3 μm. When the 50% by mass average particle diameter (D50) of the composite particles (A1) is within the above-described range, the reduction of the metal oxide constituting the outer shell proceeds efficiently, and a metal is used as a thick metal film. It is effective for forming a pattern. If the thickness is smaller than 0.1 μm, it may be inconvenient in forming a metal pattern as a thick metal film. If it is larger than 10 μm, efficient reduction of the metal oxide may be difficult.

  As a kind of metal which comprises the part which consists of a metal of a composite particle (A1), copper, silver, palladium, nickel, tungsten, ruthenium, chromium, manganese, iron, tin, zirconium, niobium, molybdenum, rhodium, zinc, for example , Lead and antimony. The portion made of metal may be formed of one kind or two or more kinds of metals.

  The metal oxide constituting the portion made of the metal oxide of the composite particle (A1) is a metal oxide constituting the portion made of the metal. For example, when the metal constituting the metal portion is copper, the metal oxide constituting the metal oxide portion is copper oxide, and the metal constituting the metal portion is silver. The metal oxide constituting the metal oxide portion is silver oxide.

The ratio of the portion made of the metal oxide in the composite particles (A1) is usually 50% by volume or less when the total volume of the composite particles (A1) is 100% by volume. When the proportion of the metal oxide portion in the composite particles (A1) is 50% by volume or less, it is easy to completely reduce the metal oxide, and it is easy to form a metal pattern as a pure metal film. .
As described above, the commercially available metal particles are usually the metal-metal oxide composite particles (A1) of the present invention.

  As the metal oxide-containing particles (A), the composite particles (A1) are preferable to the metal oxide particles (A2) from the viewpoint of forming a thick metal pattern. Since the composite particle (A1) has a core part that does not need to be reduced, it is only necessary to reduce the outer shell part. Therefore, the particle diameter can be made larger than that of the metal oxide particle (A2), which is thicker by that amount. A metal pattern can be obtained as a metal film.

When the metal particles are left in the atmosphere, the surface is usually oxidized to form metal-metal oxide composite particles (A1-1). By firing the metal particles, the surface is oxidized to form a metal. -A metal oxide composite particle (A1-1) can also be produced. The firing conditions are usually 100 ° C. to 600 ° C. and 10 minutes to 1000 minutes. By adjusting the firing conditions, the ratio of the portion made of the metal oxide in the composite particles (A1) can be appropriately determined.
Further, the particles obtained by pulverizing the composite particles (A1-1) prepared by such firing under appropriate conditions are used as particles containing the composite particles (A1-2) and the metal oxide particles (A2). can do.

[Metal oxide particles (A2)]
The metal oxide particles (A2) are particles formed from a metal oxide.
The 50% by mass average particle diameter (D50) of the metal oxide particles (A2) is preferably 0.1 μm to 5 μm, more preferably 0.1 μm to 3 μm. When the 50 mass% average particle diameter (D50) of the metal oxide particles (A2) is within the above-described range, the reduction of the metal oxide proceeds efficiently and a metal pattern is formed as a thick metal film. It is effective. If the thickness is smaller than 0.1 μm, it may be inconvenient in forming a metal pattern as a thick metal film. If it is larger than 5 μm, it may be difficult to completely reduce the metal oxide.

  Examples of the metal oxide constituting the metal oxide particles (A2) include copper, silver, gold, palladium, nickel, tungsten, ruthenium, chromium, manganese, iron, tin, zirconium, niobium, molybdenum, rhodium, zinc, Examples include oxides such as lead and antimony. The aforementioned metal oxide may be formed of one or more metal oxides.

[Alditol (B)]
When alditol (B) is contained in the second composition of this embodiment used in the metal pattern forming method of this embodiment, it acts as a reducing agent and the metal oxide contained in the metal oxide-containing particles (A). Is converted to metal.

The alditol (B) is not particularly limited as long as it has a function of reducing the metal oxide contained in the metal oxide-containing particles (A) contained in the second composition. For example, glycerin, erythritol, threitol And sugar alcohols such as ribitol, arabinitol, xylitol, allitol, sorbitol, mannitol, iditol, galactitol and taritol.
Among these, glycerin is particularly preferable because it has a strong reducing power and can efficiently form a metal pattern as a metal film from the metal oxide-containing particles (A).

  The content of alditol (B) is preferably 100 parts by mass to 1000 parts by mass, and more preferably 200 parts by mass to 800 parts by mass with respect to 100 parts by mass of the metal oxide-containing particles (A). When the content of alditol (B) is within the above-described range, the metal oxide can be efficiently reduced.

[Alditol oxide (C)]
The alditol oxide (C) is the sugar alcohol oxide exemplified as alditol (B). The alditol oxide (C) generally has a structure formed by oxidizing a hydroxyl group of alditol and converting it to a carbonyl group. In the alditol oxide (C), when the corresponding alditol has a plurality of hydroxyl groups, the number of oxidized hydroxyl groups is not particularly limited.

  Examples of the alditol oxide (C) include dihydroxyacetone and glyceraldehyde, which are glycerin oxides, and erythrose and erythrulose, which are erythritol oxides.

  The second composition used in the metal pattern forming method of the present embodiment can efficiently form a metal pattern as a metal film by containing an alditol oxide (C) together with alditol (B). Become. In particular, even a metal pattern having a large film thickness or a metal pattern made of a metal having a large ionization tendency can efficiently form a metal pattern.

The mechanism of action of the alditol oxide (C) is not necessarily clear, but is presumed as follows.
The case where the metal oxide contained in the metal oxide-containing particles (A) is a copper oxide and the alditol oxide (C) is dihydroxyacetone, which is an glycerin oxide, is taken as an example. In this example, in the process of forming a metal pattern as a metal film using the second composition, as shown in the following formula (1), between the carbonyl oxygen of dihydroxyacetone and the copper atom in the copper oxide. It is thought that a chelate bond is formed. It is considered that the reduction by alditol (B) is efficiently performed by the formation of this chelate bond. For this reason, even a metal oxide having a high ionization tendency can be efficiently reduced.

  Moreover, it is thought that the chelate bond shown by Formula (1) is formed also between the copper atom of the copper metal produced | generated by reducing copper oxide, and the carbonyl oxygen of dihydroxyacetone. By the formation of the chelate bond, the adhesion between the metal particles formed by reducing the metal oxide of the metal oxide-containing particles (A) is strengthened, and as a result, the metal oxide-containing particles (A) Even when the particle diameter of the film is large, a self-supporting film is formed, and it is considered that a metal pattern can be formed as a thick metal film.

The alditol oxide (C) may function as a reducing agent depending on the type thereof. For example, dihydroxyacetone functions as a reducing agent.
When the alditol (B) is glycerin, the glycerin (I) reduces the copper oxide in the metal oxide-containing particles (A) as shown in the following formula (2).

  At this time, in glycerin (I), for example, one hydroxyl group is oxidized to dihydroxyacetone (II) having one carbonyl group in the molecule. That is, the dihydroxyacetone (II) functions as the alditol oxide (C) together with the alditol oxide (C) originally contained in the second composition. Therefore, as shown in (III), this dihydroxyacetone (II) forms a chelate bond with the copper atom of copper oxide and the copper atom of copper metal, contributing to the formation of an efficient metal pattern as described above. I think that.

  Moreover, since this dihydroxyacetone (II) functions as a reducing agent as described above, it reduces the copper oxide in the metal oxide-containing particles (A). At this time, in dihydroxyacetone (II), for example, one hydroxyl group is oxidized to form compound (IV) having two carbonyl groups in the molecule. This compound (IV) functions as an oxide (C) of alditol. Therefore, for example, as shown in (V), this compound (IV) forms a chelate bond with the copper atom of the copper oxide and the copper atom of the metal copper to form an efficient metal pattern as described above. It is thought to contribute.

  Furthermore, since the compound (IV) also functions as a reducing agent, the copper oxide in the metal oxide-containing particles (A) is reduced. At this time, in the compound (IV), the hydroxyl group is further oxidized to become a compound having three carbonyl groups in the molecule. This compound also functions as an alditol oxide (C) and is considered to contribute to the formation of an efficient metal pattern as described above by forming a chelate bond with the copper atom of copper oxide and the copper atom of copper metal. .

  Thus, since alditol (B) becomes alditol oxide (C) by the reduction reaction of the metal oxide during the formation of the metal pattern, the concentration of alditol oxide (C) increases during the formation of the metal pattern. As described above, the effect of efficiently forming the metal pattern is further increased. Depending on the type of alditol (B), as the above-mentioned glycerin, the oxides produced one after another become the oxide (C) of alditol, so that the above-described effects are further increased.

  When the alditol oxide (C) is an alditol (B) oxide, the alditol of the same kind as the alditol oxide (C) is formed from the alditol (B) by a reduction reaction of the metal oxide during the formation of the metal pattern. An oxide (C) is produced, and the same mechanism of action as described above is obtained, which is preferable. Therefore, for example, when alditol (B) is glycerin, alditol oxide (C) is preferably dihydroxyacetone, which is an glycerin oxide.

  The content of the alditol oxide (C) in the second composition is preferably 1 part by mass to 50 parts by mass, more preferably 5 parts by mass to 30 parts by mass with respect to 100 parts by mass of the alditol (B). Part, more preferably 5 parts by mass to 20 parts by mass. When the content of the alditol oxide (C) is within such a range, it becomes easy to form an efficient metal pattern as described above.

[Other ingredients]
The 2nd composition of this embodiment used for the metal pattern formation method of this embodiment is components other than metal oxide containing particle | grains (A), alditol (B), and the oxide (C) of alditol as needed. May be contained.
For example, a 2nd composition can contain the metal particle which consists only of metals other than a metal oxide containing particle (A).

  In addition, the second composition can contain a surfactant, a viscosity modifier, an adhesion aid and the like.

[Method for Preparing Second Composition]
The 2nd composition of this embodiment used for the metal pattern formation method of this embodiment can be prepared by mixing the component mentioned above. There is no restriction | limiting in particular in a mixing method, For example, it can mix using a bead mill etc.

<Heating process>
In the heating process of the metal pattern forming method of the present embodiment, heating is performed to heat the second composition of the present embodiment filled in the removed portion of the resin layer and to remove the resin layer. By heating, the second composition filled in the removed portion of the resin layer forms a metal pattern corresponding to the shape of the removed portion. As described above, the removal portion is formed as an aperture pattern having a shape complementary to a desired metal pattern, and the formed metal pattern has a desired shape. That is, the metal pattern can have a delicate shape with a desired thin line width corresponding to the removal portion having a delicate shape with a thin line width.

  Then, when the second composition is heated, the resin layer is also heated and removed. The resin layer is formed from the first composition described above, and can be completely removed from the substrate by heating at a temperature in the range of 100 ° C to 300 ° C. That is, the resin layer can be completely removed from the substrate even by heating at 200 ° C. or lower. Therefore, only a desired metal pattern is formed on the substrate by heating in the heating step.

  The heating temperature in the heating step can be set to 50 ° C. to 300 ° C. in order to form a metal pattern from the second composition. And since it sets it as the temperature which can also remove a resin layer simultaneously, it is preferable to set to comparatively high, and it is preferable to set it as 100 to 300 degreeC. In consideration of energy saving and the use of an organic substrate for the substrate, the heating temperature in the heating step is more preferably 100 ° C. to 250 ° C., and further preferably 100 ° C. to 200 ° C. By setting the temperature condition in such a range, the resin layer can be removed and a metal pattern having excellent adhesion to the substrate can be efficiently formed in a short time. The heating time is 5 minutes to 5000 minutes, preferably 10 minutes to 120 minutes.

  Heating can be performed in several stages. For example, first, a metal pattern may be formed from the second composition by heating at a low temperature for a certain time, and then heated at a high temperature for a certain time to completely remove the resin layer.

Examples of the heating device include a hot plate and a circulation type drying furnace.
The atmosphere during heating is preferably an atmosphere that does not contain oxygen gas, such as an inert gas atmosphere, from the viewpoint of removing the resin layer and suppressing oxidation of the formed metal pattern. From the viewpoint of productivity and the like, a preferable atmosphere is an atmosphere mainly containing nitrogen gas.

  The metal pattern thus obtained can have a film thickness of 1 μm to 100 μm. As described above, since the second composition contains the alditol oxide (C), the metal oxide-containing particles (A) having a large particle diameter can be used. A metal pattern can be formed as the metal film.

  In general, in the case of a metal having a high ionization tendency such as copper, it is difficult to form a metal film because a metal oxide formed on the surface of the metal particle is difficult to be reduced. In the case of the second composition used in the metal pattern forming method of the present embodiment, even if it contains a alditol oxide (C), as described above, even a metal oxide having a high ionization tendency. Since the reduction can be sufficiently performed, a metal pattern can be efficiently formed as a metal film having a large ionization tendency, such as copper, aluminum, iron, and nickel.

  In the metal pattern forming method of the present embodiment described above, the pattern forming method of the present embodiment is performed by the resin layer forming step and the removal portion forming step to form a pattern made of a resin having a desired shape. After that, the metal pattern can be efficiently formed using the resin pattern and the second composition by the composition filling step and the heating step.

  In addition, in the metal pattern formation method of this embodiment, when a metal film is formed using the second composition of this embodiment, a large number of metal oxide-containing particles (A) adhere to each other to form a film. A metal film having voids, that is, a porous metal film may be obtained. Therefore, when the metal oxide-containing particles (A) having a large particle diameter are used for the preparation of the second composition, a metal pattern may be formed as a more porous metal film with a large proportion of voids in the interior. .

Therefore, when the metal pattern obtained from the second composition of the present embodiment becomes a film having voids, by filling the voids with metal, the metal having no voids or a small content ratio of voids A pattern can be formed.
Examples of the method of filling the voids inside the metal pattern with a metal include a method of filling the voids with a solution containing a metal element and filling the voids by generating metal from this solution.

  The solution containing a metal element is not particularly limited as long as it is a solution capable of generating a metal by heat treatment at about 50 ° C. to 300 ° C. The metal element contained in the solution containing the metal element is usually the same metal element as the metal constituting the target metal pattern, and the metal-metal oxide composite particles (A1) and metal oxide particles (A2). ) Is the same metal element as the metal element contained in. For example, when the target metal pattern is a pattern made of copper, the solution containing a metal element is a solution containing a copper element. As the solution containing copper element, a copper formate solution is preferable because metal copper is easily generated.

  Hereinafter, embodiments of the present invention will be described more specifically based on examples. However, the present invention is not limited to these examples.

[Preparation of the first composition]
[Example 1]
Under a nitrogen atmosphere, 5 g of o-phthalaldehyde was dissolved in 30 mL of commercially available dehydrated grade methylene chloride in a 100 mL three-necked flask and cooled to −78 ° C. in a dry ice / acetone bath to obtain boron trifluoride diethyl ether complex 0. .35 mL was added to initiate the polymerization. After stirring at −78 ° C. for 3 hours as it was, 0.36 mL of phenyl isocyanate was added as a polymerization end capping agent, followed by stirring at −78 ° C. for 1.5 hours. The synthesized polymer was reprecipitated in a large amount of cold methanol (0 ° C.), washed with methanol, and then recovered as a white solid. The recovered polymer was subjected to molecular weight measurement using GPC (HLC-8320 manufactured by Tosoh Corporation) under the conditions of an eluent (tetrahydrofuran) flow rate of 0.35 mL / min and a measurement temperature of 40 ° C. As a result, a polystyrene standard sample (Agilent Technology) The weight average molecular weight Mw based on the product manufactured by Easy PS-1) was 12000.

  The thermogravimetric change of the obtained polymer was measured by TG-DTA (Thermo Plus 2 TG8120 type, manufactured by Rigaku Corporation). The polymer powder was weighed in an aluminum pan and measured at a constant rate of temperature increase from 25 ° C. to 10 ° C./min in a nitrogen gas environment at atmospheric pressure of 0.2 L / min. At 225 ° C. 20 minutes after the start of the measurement, the weight decreased by 95%, indicating good thermal decomposition. About the obtained polymer, the weight decreasing rate in 100 degreeC was measured with the same method, and thermal stability was evaluated. The weight loss rate after heating at 100 ° C. for 30 minutes under a nitrogen gas environment of 0.2 L / min at atmospheric pressure was 2%, confirming thermal stability.

  Next, the obtained polymer was diluted with cyclohexanone as a solvent to prepare a solution-like first composition.

[Preparation of Second Composition]
[Example 2]
Fine electrolytic copper powder (product name “T-220”, manufactured by Mitsui Kinzoku Co., Ltd.) was baked in an oven at 200 ° C. for 1 hour in the atmosphere to form a copper oxide coating on the surface. 20 parts of finely divided electrolytic copper powder after firing, 2 parts of dihydroxyacetone and 78 parts of glycerin are placed in a bead mill together with zirconia beads, and the finely divided electrolytic copper powder after firing is pulverized to produce copper-copper oxide composite particles, copper oxide particles and copper A second composition containing 20 parts of mixed particles (particle diameter (D50): 0.2 μm), 2 parts of dihydroxyacetone and 78 parts of glycerin was prepared.

[Formation of resin pattern and metal pattern]
[Example 3]
Using the first composition of Example 1, a coating film of the first composition was formed on a silicon wafer, which is a silicon substrate, in the air by spin coating. After forming the coating film, it was heated at 80 ° C. for 1 minute to form a resin layer having a thickness of 500 μm on the silicon wafer.

  Next, using a YAG laser (model: LP-ES1, manufactured by AOV, product name: excimer laser processing machine), YAG laser light is irradiated at an output of 30 A, and processed into stripes having a line width of 100 μm and a line spacing of 100 μm. As a result, the resin layer was removed from the silicon substrate with a width of 100 μm. And the striped removal part of 100 micrometers width was formed in the resin layer, and the pattern which consists of resin was formed.

Using the second composition of Example 2, droplets were ejected into the removed portion of the pattern made of the resin formed as described above by the inkjet method, and the second composition was filled into the removed portion. .
Next, the heat treatment was performed under reduced pressure at 180 ° C. for 30 minutes in a flash annealing furnace (RHL-P610CP manufactured by ULVAC SINKU RIKO) in a nitrogen gas environment controlled at a reduced pressure of 20 torr. As a result, the resin layer was removed and a pattern made of striped copper was formed.

  The formed copper pattern had a film thickness of 25 μm, a stripe shape with a line width of 100 μm, and a space between lines of 100 μm, and no defects such as so-called pattern collapse were observed. Whether or not the obtained copper pattern was conducted was confirmed by using a tester, and the conduction was confirmed.

In addition, the measurement of the film thickness etc. of the pattern which consists of copper was performed using the Hitachi High-Tech Co., Ltd. scanning electron microscope.
From the results in the above examples, it was confirmed that a pattern made of copper could be formed as a metal pattern by using the pattern forming method and the metal pattern forming method of the present embodiment without using a plating process or a vacuum process.

  As mentioned above, although embodiment of this invention was described, this invention is not limited to the said embodiment, A various deformation | transformation can be implemented in the range which does not deviate from the summary.

  The pattern forming method and metal pattern forming method of the present invention can be suitably used particularly for circuit pattern formation of wiring boards in the electronics field. And the metal pattern of this invention can be utilized suitably for the circuit pattern of the wiring board in the electronics field | area.

DESCRIPTION OF SYMBOLS 1 Board | substrate 2 Resin layer 3 Removal part 4 2nd composition 5 Metal pattern

Claims (11)

[1] On the substrate, (a) the weight loss rate after 30 minutes at 100 ° C. is 10% or less, and (b) when the temperature is increased from 25 ° C. at 10 ° C./minute, Forming a coating film of the first composition containing a polymer having a polyacetal structure having a weight reduction rate of 80% or more, and forming a resin layer on the substrate;
[2] A step of locally heating to remove the resin layer into an arbitrary shape ;
[3] A part including the surface part of the removed part of the resin layer obtained by removing the resin layer in an arbitrary shape in the step [2], the part including the surface part. Filling a second composition containing metal-metal oxide composite particles (A1), alditol (B), and alditol oxide (C) other than the above-mentioned metal,
[4] A method of forming a metal pattern , comprising: heating and heating the second composition filled in the removal portion and removing the resin layer . 2. The metal pattern forming method according to claim 1, wherein the local heating in the step [2] is performed by irradiating a laser beam . The method for forming a metal pattern according to claim 1 or 2, wherein the polymer contained in the first composition has a repeating unit represented by the following formula (α).

(In the formula (α), X ¹ and X ² each independently represent one or more atoms or substituents selected from the group consisting of a hydrogen atom, a halogen atom, and a hydrocarbon group having 1 to 20 carbon atoms. X ³ and X ⁴ represent an atomic group having a total carbon number of 1 to 15 which is linked to each other to form one or more rings, wherein each hydrocarbon group and a hydrogen atom on the atomic group are each independently And may be substituted with an atom or a substituent selected from the group consisting of a halogen atom and an alkoxy group having 1 to 10 carbon atoms.) The said polymer which the said 1st composition contains has a repeating unit represented by a following formula ((beta)), The metal pattern formation method of any one of Claims 1-3 characterized by the above-mentioned.

(In the above formula (β), R ¹ represents one or more atoms or substituents selected from the group consisting of a halogen atom, a hydroxyl group, a hydrocarbon group having 1 to 20 carbon atoms and an alkoxy group having 1 to 4 carbon atoms. M represents an integer of 0 to 4, and n represents an integer of 5 to 1000. Here, n represents the number of repetitions of the repeating unit, and when m is 2 or more, R ¹ are the same as each other. May be different or different.) The metal pattern forming method according to any one of claims 1 to 4, wherein the polymer contained in the first composition has a terminal structure represented by the following formula (γ).

(In the above formula (γ), Z is a hydrogen atom, a hydrocarbon group having 1 to 20 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, an acyl group, a carbonyl group, an ester group and a formyl group, an amino group, and an alkylamino group. And a substituent selected from the group consisting of an arylamino group, an isocyanate group, an amide group, a nitro group and a cyano group, and a heterocyclic group containing a nitrogen atom, an oxygen atom or a sulfur atom, wherein the hydrocarbon group , An alkoxy group, an acyl group, an ester group, an alkylamino group, an arylamino group, an amide group, and a heterocyclic group include a halogen atom, a hydroxyl group, a carbonyl group, a hydrocarbon group having 1 to 20 carbon atoms, and a carbon atom. (It may be substituted with one or more selected from the group consisting of alkoxy groups of 1 to 10). The metal pattern formation according to any one of claims 1 to 5 , wherein the alditol oxide (C) contained in the second composition is an oxide of the alditol (B). Method. The metal pattern forming method according to any one of claims 1 to 6, wherein the alditol (B) contained in the second composition is glycerin . The second composition, claims content of the oxide of the alditols (C) is, relative to the alditol (B) 100 parts by weight, characterized in that it is a 1 part by weight to 50 parts by weight 1 The metal pattern formation method of any one of -7 . The filling step [3] the second composition to the removal portion of the metal pattern forming method according to any one of claims 1 to 8 which comprises using an ink jet method. The metal pattern forming method according to any one of claims 1 to 9, wherein the heating temperature in the step [4] is 100 ° C to 300 ° C. It forms using the metal pattern formation method of any one of Claims 1-10, The metal pattern characterized by the above-mentioned.

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