JP6230469B2 - TRANSFER FILM AND TRANSPARENT LAMINATE, ITS MANUFACTURING METHOD, CAPACITANCE TYPE INPUT DEVICE AND IMAGE DISPLAY DEVICE - Google Patents

Description

  The present invention relates to a transfer film and a transparent laminate, a manufacturing method thereof, a capacitance-type input device, and an image display device. Specifically, a capacitance-type input device that can detect the contact position of a finger as a change in capacitance, a transparent laminate that can be used therefor, a transfer film used for producing the transparent laminate, and a method for producing the transfer film The present invention also relates to a method for producing a transparent laminate using the transfer film, and an image display device including the capacitance type input device as a constituent element.

  In recent years, electronic devices such as mobile phones, car navigation systems, personal computers, ticket vending machines, and bank terminals have been equipped with a tablet-type input device on the surface of a liquid crystal device, etc., and an instruction image displayed in the image display area of the liquid crystal device In some cases, information corresponding to the instruction image can be input by touching a part where the instruction image is displayed with a finger or a touch pen.

  Such input devices (touch panels) include a resistance film type and a capacitance type. However, the resistance film type input device has a drawback that it has a narrow operating temperature range and is susceptible to changes over time because it has a two-layer structure of film and glass that is shorted by pressing the film.

  On the other hand, the capacitance-type input device has an advantage that a light-transmitting conductive film is simply formed on a single substrate. In such a capacitance-type input device, for example, electrode patterns are extended in directions intersecting each other, and when a finger or the like comes into contact, the capacitance between the electrodes is detected to detect the input position. (For example, refer to Patent Documents 1 to 3 below).

When using these capacitance-type input devices, for example, the transparent electrode pattern is conspicuous at a position slightly away from the vicinity of the regular reflection when the light source is reflected, and there is a problem of visibility such as poor appearance. It was. On the other hand, in Patent Document 1, an ITO pattern is formed on a substrate, a layer made of a low refractive index dielectric material such as SiO ₂ is formed only on the ITO pattern, and a high refractive index dielectric such as Nb ₂ O _5. It is described that by alternately laminating layers made of materials, the transparent electrode pattern becomes stealth and has a neutral color tone due to the light interference effect of each layer.
In Patent Document 2, before forming the ITO pattern on the substrate, a low refractive index layer such as SiO ₂ and a high refractive index layer such as Nb ₂ O ₅ are laminated only on the lower side of the ITO pattern and then the ITO pattern. It is described that the formation of the transparent electrode pattern shape can be prevented by forming.
In Patent Document 3, before forming an ITO pattern on a substrate, a low refractive index layer such as SiO ₂ and a high refractive index layer such as Nb ₂ O ₅ are laminated only on the lower side of the ITO pattern, and then ITO is used. It is described that by forming the pattern, the transparent electrode pattern pattern and the intersection between the patterns can be made inconspicuous.

  Various methods are known for forming transparent films such as transparent insulating layers and transparent protective films described in these documents. Here, in smartphones and tablet PCs equipped with a capacitive touch panel on a liquid crystal or organic EL display, a tempered glass typified by Corning's gorilla glass is used for the front plate (the surface directly touched by a finger). Developed and announced. Also, a part of the above-mentioned front plate is marketed in which an opening for installing a pressure-sensitive (pressing mechanical mechanism, not a capacitance change) switch is formed. Since these tempered glasses have high strength and are difficult to process, generally, the tempering treatment is performed after the opening is formed before the tempering treatment in order to form the aforementioned opening.

Patent Documents 4 and 5 only describe a method for forming a transparent insulating layer or a transparent protective film when an organic material is used. However, a transparent insulating layer and a transparent protective film are formed on the substrate after the strengthening process having the above-described openings by using the materials described in Patent Documents 3 and 4 by the coating method described in Patent Documents 4 and 5. If it is going to be done, the resist component leaks or protrudes from the opening, and a process of removing the protruding portion is required, resulting in a problem that the production efficiency is remarkably lowered.
Patent Document 6 discloses a thin film transfer material including a temporary support and a fine particle laminated film formed on at least one surface thereof. However, this thin film transfer material does not have photolithography suitability.

  On the other hand, Patent Documents 7 and 8 describe transfer materials for color filters, and Patent Documents 9 to 16 describe photosensitive transfer sheets for printed wiring boards, and it is proposed to laminate the transfer material on a substrate. Has been. However, although these documents mention application to a liquid crystal display device or a printed wiring board, there is no study on improving the visibility of the transparent electrode pattern (especially ITO pattern), and the capacitance There was no description of the application of transfer material to the mold input device.

JP 2010-86684 A JP 2010-152809 A JP 2010-257492 A WO 2010-061744 JP 2010-061425 A JP 2012-86477 A JP 2007-334045 A JP 2008-107779 A JP 2005-227398 A JP 2005-221857 A JP 2005-208559 A JP 2005-70765 A JP 2005-55655 A JP 2005-292734 A JP 2005-208565 A JP 2005-202066 A

  As described above, in order to solve the problem that the transparent electrode pattern is visually recognized, a method of improving using a transfer material, more specifically, a refractive index adjusting layer and an overcoat layer for improving the ITO pattern visibility. There is no disclosure regarding a transfer material for forming a pattern on a transparent electrode pattern at once using a photolithography method and a manufacturing method using the same.

  On the other hand, the present inventor has a layer structure described in Patent Documents 1 to 3 and a photosensitive transfer having a first photosensitive layer and a second photosensitive layer on a support described in Patent Documents 14 to 16. When the sheet was examined, it was found that the transparent electrode pattern was visually recognized and the problem that the transparent electrode pattern was still visually recognized could not be completely solved.

  Furthermore, a generally used capacitive input device is provided with a frame around the image display area. Therefore, when the refractive index adjustment layer is formed using a transfer film, the refractive index adjustment layer is laminated on the image display area to solve the problem of visually recognizing the transparent electrode pattern, and at the same time, the refractive index in the frame portion. It is required that the adjustment layer be easily formed into a desired pattern shape so as not to be laminated. As a method for forming a desired pattern, a method (die-cut method or half-cut method) in which the shape of the transfer film is cut according to the shape of the frame portion of the capacitive input device can be considered. However, from the viewpoint of increasing productivity, a transparent laminate having good patternability that can be developed into a desired pattern by photolithography after transferring the refractive index adjusting layer from the transfer film onto the transparent electrode pattern. It is desired to form.

  The problem to be solved by the present invention is to provide a transfer film capable of forming a transparent laminate having good patternability without causing a problem that a transparent electrode pattern is visually recognized.

The inventor adjoins the temporary support, the first curable transparent resin layer having a low refractive index adjusted to a specific refractive index range, and the second curable transparent resin layer having a high refractive index. And using a transfer film in which one of the first and second curable transparent resin layers is a water-soluble layer and the other is a water-insoluble layer on the transparent electrode pattern. A second curing obtained by transferring, exposing, developing and baking a second curable transparent resin layer having a high refractive index and a first curable resin layer having a low refractive index in a specific refractive index range. By laminating the laminated pattern of the transparent transparent resin layer and the first curable transparent resin layer on the transparent laminate of the configuration, the problem that the transparent electrode pattern is visually recognized can be solved, and the refractive index adjusting layer is transferred from the transfer film to the transparent electrode pattern. After being transferred onto the I came to find that can be developed into a pattern.
The present invention, which is a specific means for solving the above problems, is as follows.

[1] A temporary support, a first curable transparent resin layer, and a second curable transparent resin layer disposed adjacent to the first curable transparent resin layer in this order,
A layer exhibiting water solubility that completely dissolves in an immersion time within 3 minutes / μm per unit film thickness when either the first curable transparent resin layer or the second curable transparent resin layer is immersed in water. And when the other is immersed in water, it is a layer exhibiting water insolubility that does not completely dissolve in an immersion time within 3 minutes / μm per unit film thickness,
The refractive index of the second curable transparent resin layer is higher than the refractive index of the first curable transparent resin layer,
A transfer film in which the refractive index of the second curable transparent resin layer is 1.6 or more.
[2] In the transfer film according to [1], the first curable transparent resin layer and the second curable transparent resin layer each independently include a binder, a polymerizable compound, and a photopolymerizable initiator. preferable.
[3] The transfer film described in [2] was calculated by the SP value calculated by the Okitsu method of the binder contained in the water-soluble layer and by the Okitsu method of the binder contained in the water-insoluble layer. The difference from the SP value is preferably 1.02 (MPa) ^1/2 or more.
[4] In the transfer film according to [2] or [3], the binder contained in the water-soluble layer is preferably a polyvinyl alcohol derivative.
[5] In the transfer film according to [4], the polyvinyl alcohol derivative is preferably polyvinyl butyral, polyvinyl acetal, completely saponified polyvinyl alcohol or polyvinyl alcohol obtained by partially saponifying polyvinyl acetate.
[6] The transfer film according to [4] or [5] preferably has an unsubstituted hydroxyl group content of 66 mol% or more of the substituted or unsubstituted hydroxyl groups contained in the polyvinyl alcohol derivative.
[7] In the transfer film according to any one of [1] to [6], the refractive index of the first curable transparent resin layer is preferably 1.50 to 1.53.
[8] In the transfer film according to any one of [1] to [7], the water-soluble layer has a water / alcohol content of 1 to 3 carbon atoms by mass ratio of 58/42 to 100. Formed by applying a coating solution containing / 0 water or a mixed solvent,
It is preferable that the water-insoluble layer is formed by applying a coating solution containing an organic solvent.
[9] In the transfer film according to any one of [1] to [8], the thickness of the second curable transparent resin layer is preferably 500 nm or less.
[10] In the transfer film according to any one of [1] to [9], the thickness of the first curable transparent resin layer is preferably 1 to 15 μm.
[11] In the transfer film according to any one of [1] to [10], the second curable transparent resin layer preferably contains particles having a refractive index of 1.55 or more.
[12] A step of forming a first curable transparent resin layer on the temporary support;
Forming a second curable transparent resin layer directly on the first curable transparent resin layer,
Either one of the first curable transparent resin layer and the second curable transparent resin layer is water / water having an alcohol content of 1 to 3 carbon atoms in a mass ratio of 58/42 to 100/0 or mixed. Formed by applying a coating solution containing a solvent, and forming the other by applying a coating solution containing an organic solvent,
The refractive index of the second curable transparent resin layer is higher than the refractive index of the first curable transparent resin layer,
The manufacturing method of the transfer film whose refractive index of a 2nd curable transparent resin layer is 1.6 or more.
[13] In the method for producing a transfer film according to [12], the first curable transparent resin layer and the second curable transparent resin layer each independently include a binder, a polymerizable compound, and a photopolymerizable initiator. It is preferable to include.
[14] On the transparent electrode pattern, the second curable transparent resin layer and the first curable transparent resin layer of the transfer film according to any one of [1] to [11] are laminated in this order. The manufacturing method of the transparent laminated body containing a process.
[15] The method for producing a transparent laminate according to [14] preferably includes a step of simultaneously curing the first curable transparent resin layer and the second curable transparent resin layer.
[16] A transparent laminate produced by the method for producing a transparent laminate according to [14] or [15].
[17] The transparent laminate described in [16] has a refractive index of 1.6 to 1.78 on the side opposite to the side where the second curable transparent resin layer of the transparent electrode pattern is formed. It is preferable to further have a transparent film having a thickness of 55 to 110 nm.
[18] A capacitance-type input device manufactured using the transfer film according to any one of [1] to [11].
[19] A capacitance-type input device including the transparent laminate according to [16] or [17].
[20] An image display device comprising the capacitive input device according to [18] or [19] as a constituent element.

  ADVANTAGE OF THE INVENTION According to this invention, there is no problem which a transparent electrode pattern is visually recognized, and the transfer film which can form the transparent laminated body with favorable patternability can be provided.

It is a section schematic diagram showing an example of composition of an electrostatic capacity type input device of the present invention. It is a cross-sectional schematic diagram which shows another example of a structure of the electrostatic capacitance type input device of this invention. It is explanatory drawing which shows an example of the front plate in this invention. It is explanatory drawing which shows an example of the relationship between the transparent electrode pattern in this invention, and a non-pattern area | region. It is a top view which shows an example of the tempered glass in which the opening part was formed. It is a top view which shows an example of the front board in which the mask layer was formed. It is a top view which shows an example of the front plate in which the 1st transparent electrode pattern was formed. It is a top view which shows an example of the front plate in which the 1st and 2nd transparent electrode pattern was formed. It is a top view which shows an example of the front plate in which the electroconductive element different from the 1st and 2nd transparent electrode pattern was formed. It is explanatory drawing which shows a metal nanowire cross section. It is explanatory drawing which shows an example of the taper shape of the edge part of a transparent electrode pattern. It is a section schematic diagram showing an example of composition of a transparent layered product of the present invention. It is a section schematic diagram showing an example of composition of a transfer film of the present invention. It is a top view which shows another example of a structure of the electrostatic capacitance type input device of this invention, pattern exposure is carried out, and the terminal part (terminal part) of the routing wiring which is not covered with the 1st curable transparent resin layer is shown. The aspect containing is shown. An example of a state before the transfer film of the present invention having the first and second curable transparent resin layers is laminated on the transparent electrode pattern of the capacitive input device and cured by exposure or the like is shown. FIG. It is the schematic which shows an example of the desired pattern by which the 1st curable transparent resin layer and the 2nd curable transparent resin layer were hardened | cured.

  Hereinafter, the transfer film of the present invention and its manufacturing method, the transparent laminate and its manufacturing method, the capacitance-type input device and the image display device will be described. The description of the constituent elements described below may be made based on typical embodiments and specific examples of the present invention, but the present invention is not limited to such embodiments and specific examples. In the present specification, a numerical range represented by using “to” means a range including numerical values described before and after “to” as a lower limit value and an upper limit value.

[Transfer film]
The transfer film of the present invention comprises a temporary support, a first curable transparent resin layer, and a second curable transparent resin layer disposed adjacent to the first curable transparent resin layer in this order. Water solubility that completely dissolves within a period of 3 minutes / μm per unit film thickness when one of the first curable transparent resin layer and the second curable transparent resin layer is immersed in water The second curable transparent resin layer is a layer exhibiting water insolubility that is not completely dissolved in an immersion time within 3 minutes / μm per unit film thickness when the other is immersed in water. Is higher than the refractive index of the first curable transparent resin layer, and the refractive index of the second curable transparent resin layer is 1.6 or more.
By setting it as such a structure, there is no problem that a transparent electrode pattern is visually recognized and the transparent laminated body with favorable patterning property can be formed. The difference in refractive index between the transparent electrode pattern (preferably ITO) and the second curable transparent resin layer, and the second curable transparent resin layer and the first curable transparent resin layer. By reducing the difference in refractive index, light reflection is reduced and the transparent electrode pattern becomes difficult to see, and the visibility of the transparent electrode pattern can be improved. Also, the first curable transparent resin layer is laminated by either one of the first and second curable transparent resin layers being a water-soluble layer and the other being a water-insoluble layer. Then, even if the second curable transparent resin layer is laminated without curing the first curable transparent resin layer, the layer fraction is improved and the transparent electrode pattern visibility is improved by the above mechanism. In addition, the refractive index adjusting layer (that is, the first and second curable transparent resin layers) can be transferred from the transfer film onto the transparent electrode pattern and then developed into a desired pattern by photolithography. In addition, when the layer fraction of the 1st and 2nd curable transparent resin layer is bad, the effect of refractive index adjustment by said mechanism will become inadequate, and the improvement of a transparent electrode pattern visibility will become inadequate.
Furthermore, the transfer film of the present invention preferably has a good layer fraction. Moreover, it is preferable that the transfer film of this invention has a favorable crack. Moreover, it is preferable that the transparent laminated body of this invention has a favorable reticulation.

Hereinafter, preferred embodiments of the transfer film of the present invention will be described.
The transfer film of the present invention is preferably for a transparent insulating layer or a transparent protective layer of a capacitive input device. More specifically, the transfer film of the present invention is preferably used as a transfer film for forming a laminated pattern of a refractive index adjusting layer and an overcoat layer (transparent protective layer) on a transparent electrode pattern by a photolithography method. it can.

[Temporary support]
The transfer film of the present invention has a temporary support.
As the temporary support, a material that is flexible and does not cause significant deformation, shrinkage, or elongation under pressure or under pressure and heating can be used. Examples of such a temporary support include a polyethylene terephthalate film, a cellulose triacetate film, a polystyrene film, and a polycarbonate film, and among them, a biaxially stretched polyethylene terephthalate film is particularly preferable.

There is no restriction | limiting in particular in the thickness of a temporary support body, The range of 5-200 micrometers is common, and the range of 10-150 micrometers is especially preferable at points, such as handleability and versatility.
Further, the temporary support may be transparent or may contain dyed silicon, alumina sol, chromium salt, zirconium salt or the like.
Further, the temporary support can be provided with conductivity by a method described in JP-A-2005-221726.

[First curable transparent resin layer and second curable transparent resin layer]
The transfer film of the present invention has a first curable transparent resin layer and a second curable transparent resin layer disposed adjacent to the first curable transparent resin layer, and the first curable transparent resin. When either one of the resin layer and the second curable transparent resin layer is immersed in water, it is a water-soluble layer that completely dissolves in a unit thickness of 3 minutes / μm per unit film thickness, and the other is It is a non-water-soluble layer that does not dissolve completely within an immersion time of 3 minutes / μm per unit film thickness when immersed in water, and the refractive index of the second curable transparent resin layer is the first curable It is higher than the refractive index of the transparent resin layer, and the refractive index of the second curable transparent resin layer is 1.6 or more.
The first curable transparent resin layer and the second curable transparent resin layer may be thermosetting, photocurable, thermosetting and photocurable. Among them, the first curable transparent resin layer and the second curable transparent resin layer are preferably at least a thermosetting transparent resin layer, preferably from the viewpoint that the film can be thermoset after transfer to impart film reliability, A thermosetting transparent resin layer and a photocurable transparent resin layer are more preferable from the viewpoints of being photocured after transfer and easy to form a film, and thermosetting after film formation to impart film reliability.
In the present specification, for convenience of explanation, the first curable transparent resin layer and the second curable transparent resin layer of the transfer film of the present invention are transferred onto a transparent electrode pattern, and these layers are photocured. In the case where these layers have lost photo-curing properties after the first curable transparent resin layer and the second curable transparent resin layer, respectively, regardless of whether or not these layers have thermosetting properties. Call. Furthermore, after these layers are photocured, thermosetting may be performed. In this case, the first curable transparent resin layer and the second curable resin layer continue to be used regardless of whether these layers are curable. This is called a curable transparent resin layer. Similarly, after the first curable transparent resin layer and the second curable transparent resin layer of the transfer film of the present invention are transferred onto the transparent electrode pattern and these layers are thermally cured, these layers are thermosetting. If these layers are lost, these layers are referred to as the first curable transparent resin layer and the second curable transparent resin layer, respectively, regardless of whether or not these layers have photocurability.

<Material of first curable transparent resin layer and second curable transparent resin layer>
As long as the refractive index ranges as described above are satisfied, the materials of the first curable transparent resin layer and the second curable transparent resin layer are not particularly limited.
The transfer film of the present invention may be a negative type material or a positive type material.
When the transfer film of the present invention is a negative material, the first curable transparent resin layer and the second curable transparent resin layer include a metal oxide particle, a binder resin (preferably an alkali-soluble resin), and a polymerizable property. It preferably contains a compound, a polymerization initiator or a polymerization initiation system. Furthermore, an additive etc. are used, but it is not restricted to this.
In the transfer film of the present invention, it is preferable that the first curable transparent resin layer and the second curable transparent resin layer each independently contain a binder, a polymerizable compound, and a photopolymerizable initiator.

In the transfer film of the present invention, the first curable transparent resin layer and the second curable transparent resin layer may be a transparent resin film or an inorganic film.
As the above-described inorganic film, inorganic films used in JP 2010-86684 A, JP 2010-152809 A, JP 2010-257492 A, and the like can be used, which are described in these documents. From the viewpoint of controlling the refractive index, it is preferable to use an inorganic film having a laminated structure of a low refractive index material and a high refractive index material, or an inorganic film of a mixed film of a low refractive index material and a high refractive index material. As the above-described low refractive index material and the above high refractive index material, the materials used in the above-mentioned JP 2010-86684 A, JP 2010-152809 A, and JP 2010-257492 A are preferably used. I get out.
The aforementioned inorganic film may be a mixed film of SiO ₂ and Nb ₂ O ₅ , and in that case, it is more preferably a mixed film of SiO ₂ and Nb ₂ O ₅ formed by sputtering.

In the present invention, the first curable transparent resin layer and the second curable transparent resin layer are preferably transparent resin films.
The method for controlling the refractive index of the first curable transparent resin layer and the second curable transparent resin layer is not particularly limited, but a transparent resin film having a desired refractive index may be used alone, or metal particles or metal A transparent resin film to which particles such as oxide particles are added can be used, or a composite of a metal salt and a polymer can be used.

(particle)
The first curable transparent resin layer and the second curable transparent resin layer preferably contain particles for the purpose of adjusting the refractive index and light transmittance, and may contain metal oxide particles. More preferred. In particular, the second curable transparent resin layer preferably contains particles, and more preferably contains metal oxide particles. Since the metal oxide particles have high transparency and light transmittance, a positive photosensitive resin composition having a high refractive index and excellent transparency can be obtained.
The aforementioned metal oxide particles preferably have a refractive index higher than the refractive index of a composition made of a material obtained by removing the particles from the first curable transparent resin layer or the second curable transparent resin layer. . Specifically, in the transfer film of the present invention, the second curable transparent resin layer preferably contains particles having a refractive index of 1.50 or more in light having a wavelength of 400 to 750 nm. It is further preferable to contain particles of 1.55 or more, it is particularly preferred to contain particles having a refractive index of 1.70 or more, and most preferred to contain particles of 1.90 or more.
Here, that the refractive index in light having a wavelength of 400 to 750 nm is 1.50 or more means that the average refractive index in light having a wavelength in the above range is 1.50 or more. It is not necessary that the refractive index of all light having a wavelength is 1.50 or more. The average refractive index is a value obtained by dividing the sum of the measured values of the refractive index for each light having a wavelength in the above range by the number of measurement points.

The metal of the metal oxide particles described above includes metalloids such as B, Si, Ge, As, Sb, and Te.
The light-transmitting and high refractive index metal oxide particles include Be, Mg, Ca, Sr, Ba, Sc, Y, La, Ce, Gd, Tb, Dy, Yb, Lu, Ti, Zr, Hf, and Nb. Oxide particles containing atoms such as Mo, W, Zn, B, Al, Si, Ge, Sn, Pb, Sb, Bi, and Te are preferable. Titanium oxide, titanium composite oxide, zinc oxide, zirconium oxide, indium / Tin oxide and antimony / tin oxide are more preferable, titanium oxide, titanium composite oxide and zirconium oxide are more preferable, titanium oxide and zirconium oxide are particularly preferable, and titanium dioxide is most preferable. Titanium dioxide is particularly preferably a rutile type having a high refractive index. The surface of these metal oxide particles can be treated with an organic material in order to impart dispersion stability.

  From the viewpoint of transparency of the first curable transparent resin layer and the second curable transparent resin layer, the average primary particle diameter of the metal oxide particles is preferably 1 to 200 nm, particularly preferably 3 to 80 nm. Here, the average primary particle diameter of the particles refers to an arithmetic average obtained by measuring the particle diameter of 200 arbitrary particles with an electron microscope. When the particle shape is not spherical, the longest side is the diameter.

Moreover, the metal oxide particles described above may be used alone or in combination of two or more.
The content of the metal oxide particles in the first curable transparent resin layer and the second curable transparent resin layer is the same as that of the optical member obtained by the first curable transparent resin layer and the second curable transparent resin layer. What is necessary is just to determine suitably considering the required refractive index, light transmittance, etc., but with respect to the total solid content of the first curable transparent resin layer and the second curable transparent resin layer, It is preferably 80% by mass, more preferably 10-75% by mass from the viewpoint of improving the substrate adhesion of the transparent laminate of the present invention, and particularly preferably 10-70% by mass.
In the transfer film of the present invention, the first curable transparent resin layer and the second curable transparent resin layer have at least one of ZrO ₂ particles, Nb ₂ O ₅ particles, and TiO ₂ particles, as described above. From the viewpoint of controlling the refractive index within the range of the refractive index of the first curable transparent resin layer and the second curable transparent resin layer described above, ZrO ₂ particles and Nb ₂ O ₅ particles are more preferable.

(solvent)
In the case where the first or second curable transparent resin layer is a water-insoluble layer, a general organic solvent can be used. The transfer film of the present invention is preferably formed by applying the above-mentioned water-insoluble layer by applying a coating solution containing an organic solvent. For dissolving water-insoluble binders. Examples of the organic solvent include methyl ethyl ketone, propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, cyclohexanone, methyl isobutyl ketone, ethyl lactate, methyl lactate, caprolactam and the like.

When the first or second curable transparent resin layer is a water-soluble layer, water or a mixed solvent of water and a lower alcohol having 1 to 3 carbon atoms and water is preferable. In the transfer film of the present invention, the water-soluble layer is preferably formed by applying water or a mixed solvent of water and a lower alcohol having 1 to 3 carbon atoms and water. More preferably, it is formed by applying a coating solution containing water or a mixed solvent having an alcohol content of 3 in a mass ratio of 58/42 to 100/0. The water content / alcohol content of 1 to 3 carbon atoms is particularly preferably in the range of 59/41 to 100/0 in terms of mass ratio, and 60/40 to 97/3 improves the coloration of the transparent laminate of the present invention. 62/38 to 95/5 is more particularly preferable from the viewpoint of improving the substrate adhesion of the transparent laminate of the present invention and from the viewpoint of improving the reticulation of the transfer film of the present invention. Most preferred is ~ 85/15.
A mixed solvent of water, water and methanol, and a mixed solvent of water and ethanol are preferable, and a mixed solvent of water and methanol is preferable from the viewpoint of drying and coating properties.
In particular, when forming a second curable transparent resin layer, when using a mixed solvent of water and methanol, the mass ratio (mass% ratio) of water / methanol is preferably 58/42 to 100/0, The range of 59/41 to 100/0 is more preferable, 60/40 to 97/3 is particularly preferable, 62/38 to 95/5 is more preferable, and 62/38 to 85/15 is more preferable. If the content of water / alcohol having 1 to 3 carbon atoms is greater than the mass ratio of 58/42, the first curable transparent resin layer is not preferable because it dissolves or becomes cloudy.
By controlling to the said range, application | coating and quick drying are realizable without a 1st curable transparent resin layer and layer mixing.

A layer exhibiting water solubility that completely dissolves in an immersion time within 3 minutes / μm per unit film thickness when either the first curable transparent resin layer or the second curable transparent resin layer is immersed in water. And the other is a water-insoluble layer that does not completely dissolve in an immersion time within 3 minutes / μm per unit film thickness when immersed in water.
In the present invention, the fact that one of the first and second curable transparent resin layers is a water-soluble layer specifically indicates the following.
On a 75 μm thick polyethylene terephthalate film (temporary support), using a slit nozzle, the first and second curable transparent resin layer coating liquids are adjusted and applied to have a desired film thickness. . If the first or second curable transparent resin layer coating solution is repelled by the temporary support and cannot be applied, a hydrophilic treatment is performed in advance by corona treatment. After the coating film of the first or second curable transparent resin layer coating liquid is dried at 100 ° C. for 2 minutes, the coating film is further dried at 120 ° C. for 1 minute to obtain the first and second curable transparent resin layers. Form.
The first or second curable transparent resin layer is conditioned at 23 ° C. and 55% relative humidity for 1 hour and immersed in 25 ° C. ion exchange water. The immersion time is 3 minutes / μm per unit film thickness, that is, the film thickness of the first or second curable transparent resin layer (μm) ÷ 1 (μm) × 3 minutes (for example, 15 minutes in the case of 5 μm) , 80 nm is 14.4 seconds).
After the immersion, the surface was rinsed lightly with ion-exchanged water contained in a washing bottle, and the state where the entire surface was completely removed was regarded as water-soluble. Otherwise, it was regarded as water-insoluble.

The transfer film of the present invention has a difference between the SP value calculated by the Okitsu method of the binder contained in the water-soluble layer and the SP value calculated by the Okitsu method of the binder contained in the water-insoluble layer. It is preferably 1.02 (MPa) ^1/2 or more, more preferably 1.53 (MPa) ^1/2 or more, and particularly preferably 2.04 (MPa) ^1/2 or more.
There is no particular limitation on the difference between the SP value calculated by the Okitsu method of the binder contained in the water-soluble layer and the SP value calculated by the Okitsu method of the binder contained in the water-insoluble layer, but 8 0.5 (MPa) ^1/2 or less, more preferably 8.0 (MPa) ^1/2 or less, particularly preferably 7.5 (MPa) ^1/2 or less, 7 More preferably, it is 0.0 (MPa) ^1/2 or less.
In addition, SP value as used in the field of this invention is a solubility parameter computed by the Okitsu method (adhesion 38 6-6 (1994) polymer publication society), and is a unit (MPa) ^1/2 . The SP value is obtained by giving a molar attractive constant and a molar volume to each unit in the molecular structure.

(binder)
In the transfer film of the present invention, known binders can be used for the first curable transparent resin layer and the second curable transparent resin layer.
The binder used for the first or second curable transparent resin layer and having a solubility in water or a mixed solvent of a lower alcohol having 1 to 3 carbon atoms and water is particularly provided that it does not contradict the gist of the present invention. There is no restriction | limiting and it can select suitably from well-known things. For example, polyvinyl ether / maleic anhydride polymer, water-soluble salt of carboxyalkyl cellulose, water-soluble cellulose ethers, water-soluble carboxyalkyl starch described in JP-A-46-2121 and JP-B-56-40824 Salt, polyvinyl alcohol, polyvinyl alcohol derivatives such as water-soluble polyvinyl butyral and water-soluble polyvinyl acetal, polyvinyl pyrrolidone, various polyacrylamides, various water-soluble polyamides, water-soluble salts of polyacrylic acid, gelatin, ethylene oxide polymer, Water soluble salts of the group consisting of various starches and the like, styrene / maleic acid copolymers, maleate resins and the like.

  Among these polymers, the binder contained in the water-soluble layer is preferably a polyvinyl alcohol derivative, particularly polyvinyl butyral, polyvinyl acetal, fully saponified polyvinyl alcohol or polyvinyl alcohol obtained by partially saponifying polyvinyl acetate. preferable.

In the present invention, among the substituted or unsubstituted hydroxyl groups contained in the binder used in the water-soluble layer, the content of unsubstituted hydroxyl groups is preferably 66 mol% or more, and preferably 70 mol% or more. More preferable from the viewpoint of solubility. Of the substituted or unsubstituted hydroxyl groups contained in the binder used in the water-soluble layer, the unsubstituted hydroxyl group content is preferably 99.9 mol% or less.
From the viewpoint of improving the coloring of the transparent laminate of the present invention, the hydroxyl group content of the binder used in the water-soluble layer of the first and second curable transparent resin layers may be 75 mol% or more. More preferred.
From the viewpoint of improving the patternability of the transparent laminate of the present invention and improving the reticulation of the transfer film of the present invention, a layer exhibiting water solubility among the first and second curable transparent resin layers It is more preferable that the binder used in the preparation has a hydroxyl group content of 97% by mass or less.
The number of moles of hydroxyl groups contained in the polyvinyl alcohol derivative is preferably in the range of 66 mol% to 99.9 mol%. If it is 66 mol% or more, the solubility is sufficient, and if it is 99.9 mol% or less, the coating solution is difficult to gel with time, which is preferable.

  A resin (referred to as a binder or a polymer) that is used in the first curable transparent resin layer and the second curable transparent resin layer described above and is soluble in an organic solvent is contrary to the spirit of the present invention. As long as it is not particularly limited, it can be appropriately selected from known ones, and an alkali-soluble resin is preferable. Examples of the alkali-soluble resin include those described in paragraph 0025 of JP2011-95716A and JP2010-237589A. The polymers described in paragraphs 0033 to 0052 can be used.

The hydroxyl value of the polymer contained in the first curable transparent resin layer is preferably 40 mgKOH / g or less from the viewpoint of preventing corrosion of the metal wiring.
In the case of the second curable transparent resin layer, when the second curable transparent resin layer is extremely thin, there is not much adverse effect due to the hydroxyl value of the polymer.

  The first curable transparent resin layer or the second curable transparent resin layer may contain a polymer latex. The polymer latex referred to herein is a polymer in which water-insoluble polymer fine particles are dispersed in water. The polymer latex is described, for example, in Soichi Muroi, “Polymer Latex Chemistry (published by Kobunshi Shuppankai (Showa 48))”.

Polymer particles that can be used include acrylic, vinyl acetate, rubber (for example, styrene-butadiene, chloroprene), olefin, polyester, polyurethane, polystyrene, and copolymers thereof. Particles are preferred.
It is preferable to increase the bonding force between the polymer chains constituting the polymer particles. Examples of means for strengthening the bonding force between polymer chains include a method using a hydrogen bond interaction and a method of generating a covalent bond. As a means for imparting hydrogen bonding strength, it is preferable to introduce a monomer having a polar group in the polymer chain by copolymerization or graft polymerization. As polar groups, carboxyl groups (containing in acrylic acid, methacrylic acid, itaconic acid, fumaric acid, maleic acid, crotonic acid, partially esterified maleic acid, etc.), primary, secondary and tertiary amino groups, ammonium base, Examples thereof include a sulfonic acid group (styrene sulfonic acid), and a carboxyl group and a sulfonic acid group are particularly preferable.
The preferable range of the copolymerization ratio of the monomer having these polar groups is 5 to 35% by mass, more preferably 5 to 20% by mass, and further preferably 15 to 20% by mass with respect to 100% by mass of the polymer. It is. On the other hand, as means for generating a covalent bond, a hydroxyl group, carboxyl group, primary, secondary amino group, acetoacetyl group, sulfonic acid, etc., epoxy compound, blocked isocyanate, isocyanate, vinyl sulfone compound, aldehyde compound, The method of making a methylol compound, a carboxylic acid anhydride, etc. react is mentioned.
Among the polymers utilizing these reactions, polyurethane derivatives obtained by the reaction of polyols and polyisocyanate compounds are preferred, polyvalent amines are more preferred as chain extenders, and the above polar groups are introduced into the polymer chains. The ionomer type is particularly preferred.
The mass average molecular weight of the polymer is preferably 10,000 or more, more preferably 20,000 to 100,000. Suitable polymers for the present invention include ethylene ionomers and polyurethane ionomers which are copolymers of ethylene and methacrylic acid.

The polymer latex that can be used in the present invention may be obtained by emulsion polymerization or may be obtained by emulsification. The method for preparing these polymer latexes is described, for example, in “Emulsion Latex Handbook” (edited by Emulsion Latex Handbook Editorial Committee, published by Taiseisha Co., Ltd. (Showa 50)).
Examples of the polymer latex that can be used in the present invention include an aqueous dispersion of polyethylene ionomer (trade name: Chemipearl S120, manufactured by Mitsui Chemicals, Inc., solid content 27%), Chemipearl S100, manufactured by Mitsui Chemicals, Inc. Solid content 27%), Chemipearl S111, manufactured by Mitsui Chemicals, Inc. Solid content 27%), Chemipearl S200, manufactured by Mitsui Chemicals, Inc. Solid content 27%), Chemipearl S300, manufactured by Mitsui Chemicals, Inc. Solid content 35%), Chemipearl S650, manufactured by Mitsui Chemicals. Solid content 27%), Chemipearl S75N, manufactured by Mitsui Chemicals, Inc. 24% solid content) and aqueous dispersion of polyether polyurethane (trade name: Hydran WLS-201 manufactured by DIC Corporation. Solid content 35%, Tg-50 ° C) (trade name: Hydran WLS-202 DIC Corporation) (Product name: Hydran WLS-221 DIC Co., Ltd. Solid content 35%, Tg-30 ° C) (Product name: Hydran WLS-210 DIC Co., Ltd.) (35% solid content, Tg-15 ° C) (trade name: Hydran WLS-213 manufactured by DIC Corporation. 35% solid content, Tg-15 ° C) (trade name: manufactured by Hydran WLI-602 DIC Co., Ltd.) (Trade name: Hydran WLI-611 manufactured by DIC Corporation. Solid content: 39.5%, Tg-15 ° C.), ammonium acrylate copolymer ( Product name: Jurimer AT-210 made by Nippon Pure Chemical Co., Ltd., alkyl acrylate copolymer ammonium (trade name: Jurimer ET-410 made by Nippon Pure Chemical Co., Ltd.), alkyl acrylate copolymer ammonium (product name: Jurimer AT-510 made by Nippon Pure Chemical Co., Ltd.), A product obtained by neutralizing and emulsifying polyacrylic acid (trade name: Jurimer AC-10L, manufactured by Nippon Pure Chemical) with ammonia can be mentioned.

その他の水溶性を示す層に用いられる重合性化合物としては、水もしくは炭素原子数１乃至３の低級アルコールと水の混合溶媒に対して溶解性を有する重合性化合物としては、水酸基を有するモノマー、分子内にエチレンオキサイドやポリプロピレンオキサイド、及びリン酸基を有するモノマーが使用できる。
一方、非水溶性を示す層に用いられる重合性化合物としては、ポリエチレングリコールジ（メタ）アクリレート、ポリプロピレングリコールジ（メタ）アクリレート、トリメチロールエタントリアクリレート、トリメチロールプロパントリアクリレート、トリメチロールプロパンジアクリレート、ネオペンチルグリコールジ（メタ）アクリレート、ペンタエリトリトールテトラ（メタ）アクリレート、ペンタエリトリトールトリ（メタ）アクリレート、ジペンタエリトリトールヘキサ（メタ）アクリレート、ジペンタエリトリトールペンタ（メタ）アクリレート、ヘキサンジオールジ（メタ）アクリレート、トリメチロールプロパントリ（アクリロイルオキシプロピル）エーテル、トリ（アクリロイルオキシエチル）イソシアヌレート、トリ（アクリロイルオキシエチル）シアヌレート、グリセリントリ（メタ）アクリレート、トリメチロールプロパンやグリセリン、ビスフェノール等の多官能アルコールに、エチレンオキサイドやプロピレンオキサイドを付加反応した後で（メタ）アクリレート化したもの、特公昭４８−４１７０８号、特公昭５０−６０３４号、特開昭５１−３７１９３号等の各公報に記載されているウレタンアクリレート類；特開昭４８−６４１８３号、特公昭４９−４３１９１号、特公昭５２−３０４９０号等の各公報に記載されているポリエステルアクリレート類；エポキシ樹脂と（メタ）アクリル酸の反応生成物であるエポキシアクリレート類等の多官能アクリレートやメタクリレートなどが挙げられる。これらの中でも、トリメチロールプロパントリ（メタ）アクリレート、ペンタエリトリトールテトラ（メタ）アクリレート、ジペンタエリトリトールヘキサ（メタ）アクリレート、ジペンタエリトリトールペンタ（メタ）アクリレートペンタエリスリトールテトラアクリレート混合物（ＮＫエステル Ａ−ＴＭＭＴ新中村化学工業（株）製）、ペンタエリスリトールエチレンオキサイド（ＥＯ）付加物のテトラアクリレート（カヤラッドＲＰ−１０４０ 日本化薬（株）製）を好ましく用いることができる。が特に好ましい。これらは、１種単独で使用してもよいし、２種以上を併用してもよい。 (Polymerizable compound)
As the polymerizable compound used in the water-soluble layer or the water-insoluble layer, the polymerizable compounds described in paragraphs 0023 to 0024 of Japanese Patent No. 4098550 can be used. Among these, pentaerythritol tetraacrylate, pentaerythritol triacrylate, and tetraacrylate of pentaerythritol ethylene oxide (EO) adduct can be preferably used. These polymerizable compounds may be used alone or in combination. When a mixture of pentaerythritol tetraacrylate and pentaerythritol triacrylate is used, the ratio of pentaerythritol triacrylate is preferably 0 to 80%, more preferably 10 to 60% in terms of mass ratio.
In the present invention, as a polymerizable compound, specifically, a water-soluble polymerizable compound represented by the following structural formula 1, pentaerythritol tetraacrylate mixture (NK ester A-TMMT, manufactured by Shin-Nakamura Chemical Co., Ltd., as an impurity) About 10% triacrylate), mixture of pentaerythritol tetraacrylate and triacrylate (NK ester A-TMM3LM-N, Shin Nakamura Chemical Co., Ltd., 37% triacrylate), mixture of pentaerythritol tetraacrylate and triacrylate ( NK ester A-TMM-3L Shin-Nakamura Chemical Co., Ltd., triacrylate 55%), mixture of pentaerythritol tetraacrylate and triacrylate (NK ester A-TMM3 Shin-Nakamura Chemical Co., Ltd., triacrylate 57% ), Penta Examples thereof include tetraacrylate of erythritol ethylene oxide (EO) adduct (Kayarad RP-1040, Nippon Kayaku Co., Ltd.).
Among these, as the polymerizable compound used in the water-soluble layer, from the viewpoint of improving the reticulation of the transfer film of the transfer film of the present invention, the water-soluble polymerizable property represented by the following structural formula 1 Compound, pentaerythritol tetraacrylate mixture (NK ester A-TMMT, Shin-Nakamura Chemical Co., Ltd.), pentaerythritol tetraacrylate and triacrylate mixture (NK ester A-TMM3LM-N, Shin-Nakamura Chemical Co., Ltd., Tri Acrylate 37%), a mixture of pentaerythritol tetraacrylate and triacrylate (NK ester A-TMM-3L, Shin-Nakamura Chemical Co., Ltd., triacrylate 55%) can be preferably used.

Examples of the polymerizable compound used in the other water-soluble layer include a monomer having a hydroxyl group as a polymerizable compound having solubility in water or a mixed solvent of a lower alcohol having 1 to 3 carbon atoms and water. A monomer having ethylene oxide, polypropylene oxide and a phosphate group in the molecule can be used.
On the other hand, the polymerizable compound used for the layer showing water insolubility is polyethylene glycol di (meth) acrylate, polypropylene glycol di (meth) acrylate, trimethylolethane triacrylate, trimethylolpropane triacrylate, trimethylolpropane diacrylate. , Neopentyl glycol di (meth) acrylate, pentaerythritol tetra (meth) acrylate, pentaerythritol tri (meth) acrylate, dipentaerythritol hexa (meth) acrylate, dipentaerythritol penta (meth) acrylate, hexanediol di (meth) Acrylate, trimethylolpropane tri (acryloyloxypropyl) ether, tri (acryloyloxyethyl) isocyanurate, tri (Acryloyloxyethyl) cyanurate, glycerin tri (meth) acrylate, polyfunctional alcohols such as trimethylolpropane, glycerin, bisphenol, etc., and (meth) acrylate after addition reaction of ethylene oxide or propylene oxide. Urethane acrylates described in JP-A-41708, JP-B-50-6034, JP-A-51-37193, etc .; JP-A-48-64183, JP-B-49-43191, JP-B-52-30490 Polyester acrylates described in various publications such as No .; polyfunctional acrylates and methacrylates such as epoxy acrylates which are reaction products of epoxy resin and (meth) acrylic acid. Among these, trimethylolpropane tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol hexa (meth) acrylate, dipentaerythritol penta (meth) acrylate pentaerythritol tetraacrylate mixture (NK ester A-TMMT new) Nakamura Chemical Co., Ltd.) and tetraacrylate of pentaerythritol ethylene oxide (EO) adduct (Kayarad RP-1040, Nippon Kayaku Co., Ltd.) can be preferably used. Is particularly preferred. These may be used individually by 1 type and may use 2 or more types together.

一方、非水溶性を示す層に用いられる光重合開始剤または重合開始系としては、特開２０１１−９５７１６号公報に記載の段落００３１〜００４２に記載の光重合開始剤を用いることができる。例えば、１，２−オクタンジオン，１−［４−（フェニルチオ）−，２−（Ｏ−ベンゾイルオキシム）］（商品名：ＩＲＧＡＣＵＲＥ ＯＸＥ−０１、ＢＡＳＦ製）の他、エタノン，１−［９−エチル−６−（２−メチルベンゾイル）−９Ｈ−カルバゾール−３−イル］−，１−（０−アセチルオキシム）商品名：ＩＲＧＡＣＵＲＥ ＯＸＥ−０２、ＢＡＳＦ製）、２−（ジメチルアミノ）−２−［（４−メチルフェニル）メチル］−１−［４−（４−モルホリニル）フェニル］−１−ブタノン（商品名：ＩＲＧＡＣＵＲＥ ３７９ＥＧ、ＢＡＳＦ製）、２−メチル−１−（４−メチルチオフェニル）−２−モルフォリノプロパン−１−オン（商品名：ＩＲＧＡＣＵＲＥ ９０７、ＢＡＳＦ製）、２−ヒロドキシ−１−｛４−［４−（２−ヒドロキシ−２−メチル−プロピオニル）−ベンジル］フェニル｝−２−メチル−プロパン−１−オン（商品名：ＩＲＧＡＣＵＲＥ １２７、ＢＡＳＦ製）、２−ベンジル−２−ジメチルアミノ−１−（４−モルフォリノフェニル）−ブタノン−１（商品名：ＩＲＧＡＣＵＲＥ ３６９、ＢＡＳＦ製）、２−ヒドロキシ−２−メチル−１−フェニル−プロパン−１−オン（商品名：ＩＲＧＡＣＵＲＥ １１７３、ＢＡＳＦ製）、１−ヒドロキシ−シクロヘキシル−フェニル−ケトン（商品名：ＩＲＧＡＣＵＲＥ １８４、ＢＡＳＦ製）、２，２−ジメトキシ−１，２−ジフェニルエタン−１−オン（商品名：ＩＲＧＡＣＵＲＥ ６５１、ＢＡＳＦ製）、オキシムエステル系の（商品名：Ｌｕｎａｒ ６、ＤＫＳＨジャパン株式会社製 などを好ましく用いることができる。 (Photopolymerization initiator)
IRGACURE 2959 or an initiator represented by the following structural formula 2 can be used as a photopolymerizable initiator having solubility in water or a mixed solvent of lower alcohol having 1 to 3 carbon atoms and water.

On the other hand, as the photopolymerization initiator or the polymerization initiation system used for the water-insoluble layer, the photopolymerization initiators described in paragraphs 0031 to 0042 described in JP 2011-95716 A can be used. For example, in addition to 1,2-octanedione, 1- [4- (phenylthio)-, 2- (O-benzoyloxime)] (trade name: IRGACURE OXE-01, manufactured by BASF), ethanone, 1- [9- Ethyl-6- (2-methylbenzoyl) -9H-carbazol-3-yl]-, 1- (0-acetyloxime) trade name: IRGACURE OXE-02, manufactured by BASF), 2- (dimethylamino) -2- [(4-Methylphenyl) methyl] -1- [4- (4-morpholinyl) phenyl] -1-butanone (trade name: IRGACURE 379EG, manufactured by BASF), 2-methyl-1- (4-methylthiophenyl)- 2-morpholinopropan-1-one (trade name: IRGACURE 907, manufactured by BASF), 2-hydroxy-1- {4- [4- (2-hydroxy) Cy-2-methyl-propionyl) -benzyl] phenyl} -2-methyl-propan-1-one (trade name: IRGACURE 127, manufactured by BASF), 2-benzyl-2-dimethylamino-1- (4-morpholino Phenyl) -butanone-1 (trade name: IRGACURE 369, manufactured by BASF), 2-hydroxy-2-methyl-1-phenyl-propan-1-one (trade name: IRGACURE 1173, manufactured by BASF), 1-hydroxy-cyclohexyl -Phenyl-ketone (trade name: IRGACURE 184, manufactured by BASF), 2,2-dimethoxy-1,2-diphenylethane-1-one (trade name: IRGACURE 651, manufactured by BASF), oxime ester type (trade name: Use Lunar 6, DKSH Japan, etc. preferably Can do.

  In addition to binders having solubility in water or a mixed solvent of lower alcohol having 1 to 4 carbon atoms and water, resins used for transparent resin films (referred to as binders and polymers) and other additives include: The first curable transparent resin layer and the second curable transparent resin layer can be laminated, and are not particularly limited as long as they do not contradict the gist of the present invention, and the second curable transparent film described above in the transfer film of the present invention. Resins used for the resin layer and other additives can be preferably used.

  Furthermore, you may use an additive for the above-mentioned 1st curable transparent resin layer and the above-mentioned 2nd curable transparent resin layer. Examples of the additive include surfactants described in paragraph 0017 of Japanese Patent No. 4502784, paragraphs 0060-0071 of JP-A-2009-237362, and thermal polymerization described in paragraph 0018 of Japanese Patent No. 4502784. In addition, other additives described in paragraphs 0058 to 0071 of JP-A No. 2000-310706 may be used.

  As described above, the case where the transfer film of the present invention is a negative type material has been mainly described. However, the transfer film of the present invention may be a positive type material. When the transfer film of the present invention is a positive type material, for example, the material described in JP-A-2005-221726 is used for the first curable transparent resin layer and the second curable transparent resin layer. Used, but not limited to this.

<Configuration of first curable transparent resin layer>
In the transfer film of the present invention, the refractive index of the first curable transparent resin layer is preferably 1.5 to 1.53, more preferably 1.5 to 1.52. It is especially preferable that it is .51-1.52.

  The transfer film of the present invention is sufficient when the thickness of the first curable transparent resin layer described above is used to form the transparent protective layer of the capacitive input device using the first curable transparent resin layer. From the viewpoint of exerting the surface protecting ability, it is preferably 1 μm or more, more preferably 1 to 15 μm, particularly preferably 2 to 12 μm, and particularly preferably 3 to 10 μm.

  As the material for the first curable transparent resin layer, any polymer component or any polymerizable compound component can be used without particular limitation, but from the viewpoint of using it as a transparent protective film of a capacitive input device, Those having high surface hardness and high heat resistance are preferred. Among the alkali-soluble resins and the polymerizable compounds contained in the first curable transparent resin layer and the second curable transparent resin layer, the known photosensitivity is used. A siloxane resin material or an acrylic resin material is preferably used.

In the transfer film of the present invention, the first curable transparent resin layer described above contains the aforementioned polymerizable compound and the aforementioned photopolymerization initiator, whereby the first curable transparent resin layer and the aforementioned second curable transparent resin layer. A pattern of the curable transparent resin layer can be easily formed.
In the first curable transparent resin layer, the photopolymerization initiator is preferably contained in an amount of 1% by mass or more based on the solid content of the first curable transparent resin layer. More preferably, it is contained. In the first curable transparent resin layer, the photopolymerization initiator is preferably contained in an amount of 10% by mass or less based on the solid content of the first curable transparent resin layer. It is more preferable that it is contained below from the viewpoint of improving the patterning property, coloring property, and substrate adhesion of the transparent laminate of the present invention.

  The first curable transparent resin layer described above may or may not contain metal oxide particles. In order to control the refractive index of the above-mentioned first curable transparent resin layer within the above-mentioned range, metal oxide particles can be included at an arbitrary ratio depending on the type of polymer or polymerizable compound used. In the first curable transparent resin layer, the metal oxide particles described above are preferably included in an amount of 0 to 35% by mass with respect to the solid content of the first curable transparent resin layer. It is more preferable that 10% by mass is contained, and it is particularly preferable that it is not included.

<Configuration of second curable transparent resin layer>
The transfer film of the present invention is disposed adjacent to the first curable transparent resin layer, has a refractive index higher than that of the first curable transparent resin layer, and a refractive index of 1.6. It has the 2nd curable transparent resin layer which is the above.
In the transfer film of the present invention, the refractive index of the second curable transparent resin layer is preferably 1.60 or more.
On the other hand, the upper limit of the refractive index of the second curable transparent resin layer is not particularly limited, but is preferably 2.1 or less, more preferably 1.78 or less, and 1.74. It may be the following.

  In the transfer film of the present invention, the film thickness of the second curable transparent resin layer described above is preferably 500 nm or less, and more preferably 110 nm or less. The film thickness of the second curable transparent resin layer is preferably 20 nm or more. The film thickness of the second curable transparent resin layer is particularly preferably from 55 to 100 nm, more preferably from 60 to 100 nm, and even more preferably from 70 to 100 nm.

  In the transfer film of the present invention, it is preferable that the above-mentioned second curable transparent resin layer contains the above-described polymerizable compound from the viewpoint of curing and increasing the strength of the film.

  The second curable transparent resin layer described above may or may not include metal oxide particles, but the metal oxide particles may be included in the above-described range. It is preferable from the viewpoint of controlling the refractive index of the transparent resin layer. The above-mentioned second curable transparent resin layer can contain metal oxide particles in any proportion depending on the type of polymer or polymerizable compound used. In the layer, the metal oxide particles are preferably contained in an amount of 40 to 95% by mass, more preferably 55 to 95% by mass, based on the solid content of the second curable transparent resin layer. From the viewpoint of improving the crack of the transfer film of the present invention, it is particularly preferable that 62 to 90% by mass is contained, and 62 to 75% by mass of the transfer film of the present invention further improves the crack, and It is more particularly preferable from the viewpoint of improving the substrate adhesion of the transparent laminate of the present invention, and even more preferably 62 to 70% by mass.

<Third curable transparent resin layer>
In the transfer film of the present invention, a third curable transparent resin layer may be further provided on the second curable transparent resin layer.
When the second curable transparent resin layer is water-soluble, the third curable transparent resin layer is preferably water-insoluble, and when the second curable transparent resin layer is water-insoluble, The three curable transparent resin layers are preferably water-soluble.
The refractive index of the third curable transparent resin layer is preferably 1.60 or more.
On the other hand, the upper limit of the refractive index of the above-mentioned third curable transparent resin layer is not particularly limited, but is preferably 1.78 or less, and may be 1.74 or less.

  In the transfer film of the present invention, the thickness of the third curable transparent resin layer is preferably 500 nm or less, and more preferably 110 nm or less. The thickness of the third curable transparent resin layer is particularly preferably from 55 to 100 nm, more preferably from 60 to 100 nm, and even more preferably from 70 to 100 nm.

  In the transfer film of the present invention, it is preferable that the above-mentioned third curable transparent resin layer contains the above-described polymerizable compound from the viewpoint of curing and increasing the strength of the film.

  The above-mentioned third curable transparent resin layer may or may not contain metal oxide particles, but the inclusion of metal oxide particles in the above-mentioned range includes the above-mentioned third curable properties. It is preferable from the viewpoint of controlling the refractive index of the transparent resin layer. The above-mentioned third curable transparent resin layer can contain metal oxide particles in an arbitrary ratio depending on the type of polymer or polymerizable compound used. In the layer, the metal oxide particles are preferably contained in an amount of 40 to 95% by mass, more preferably 55 to 95% by mass, based on the solid content of the third curable transparent resin layer. 82 to 90% by mass is particularly preferable.

[Thermoplastic resin layer]
In the transfer film of the present invention, a thermoplastic resin layer can be provided between the temporary support and the first curable transparent resin layer. Using the transfer film having the thermoplastic resin layer described above, the first curable transparent resin layer and the second curable transparent resin layer are transferred to form a transparent laminate. Air bubbles are less likely to be generated, image unevenness and the like are less likely to occur in the image display device, and excellent display characteristics can be obtained.
The thermoplastic resin layer described above is preferably alkali-soluble. The thermoplastic resin layer plays a role as a cushioning material so as to be able to absorb unevenness of the base surface (including unevenness due to already formed images, etc.), and according to the unevenness of the target surface. It is preferable to have a property that can be deformed.

  The thermoplastic resin layer preferably includes an organic polymer substance described in JP-A-5-72724 as a component. The Vicat method [specifically, a polymer by American Material Testing Method ASTM D1235] An embodiment containing at least one selected from organic polymer substances having a softening point of about 80 ° C. or less according to the softening point measurement method] is particularly preferable.

  Specifically, polyolefins such as polyethylene and polypropylene, ethylene copolymers with ethylene and vinyl acetate or saponified products thereof, copolymers of ethylene and acrylic acid esters or saponified products thereof, polyvinyl chloride and vinyl chloride, Vinyl chloride copolymer with vinyl acetate or saponified product thereof, polyvinylidene chloride, vinylidene chloride copolymer, polystyrene, styrene copolymer with styrene and (meth) acrylic acid ester or saponified product thereof, polyvinyl toluene, Vinyl toluene copolymer of vinyl toluene and (meth) acrylic acid ester or saponified product thereof, poly (meth) acrylic acid ester, (meth) acrylic acid ester copolymer weight of butyl (meth) acrylate and vinyl acetate, etc. Coalescence, vinyl acetate copolymer nylon, copolymer nylon, - alkoxymethyl nylon, and organic polymers such as polyamide resins such as N- dimethylamino nylon.

  The layer thickness of the thermoplastic resin layer is preferably 3 to 30 μm. When the thickness of the thermoplastic resin layer is less than 3 μm, followability at the time of lamination may be insufficient, and unevenness on the base surface may not be completely absorbed. In addition, when the layer thickness exceeds 30 μm, a load is applied to drying (solvent removal) at the time of forming the thermoplastic resin layer on the temporary support, or it takes time to develop the thermoplastic resin layer, May deteriorate process suitability. As a layer thickness of the above-mentioned thermoplastic resin layer, 4-25 micrometers is still more preferable, and 5-20 micrometers is especially preferable.

  The thermoplastic resin layer can be formed by applying a preparation liquid containing a thermoplastic organic polymer, and the preparation liquid used for the application can be prepared using a solvent. The solvent is not particularly limited as long as it can dissolve the polymer component constituting the thermoplastic resin layer, and examples thereof include methyl ethyl ketone, cyclohexanone, propylene glycol monomethyl ether acetate (MMPGAc), n-propanol, and 2-propanol. Can be mentioned.

(Viscosity of thermoplastic resin layer and photocurable resin layer)
The viscosity of the thermoplastic resin layer measured at 100 ° C. is in the region of 1000 to 10,000 Pa · sec, the viscosity of the photocurable resin layer measured at 100 ° C. is in the region of 2000 to 50000 Pa · sec, and the following formula It is preferable to satisfy (A).

[Middle layer]
In the transfer film of the present invention, an intermediate layer can be provided between the thermoplastic resin layer and the first curable transparent resin layer. The intermediate layer is described as “separation layer” in JP-A-5-72724.

〔Protective film〕
In the transfer film of the present invention, it is preferable to further provide a protective film (hereinafter also referred to as “protective release layer”) on the surface of the second curable transparent resin layer.

  As the above-described protective film, protective films described in paragraphs 0083 to 0087 and 0093 of JP-A-2006-259138 can be appropriately used.

  In FIG. 12, an example of the preferable structure of the transfer film of this invention is shown. FIG. 12 shows a book in which a temporary support 26, a first curable transparent resin layer 7, a second curable transparent resin layer 12, and a protective release layer (protective film) 29 are laminated adjacent to each other in this order. It is the schematic of the transfer film 30 of invention.

[Transfer Film Manufacturing Method]
The transfer film of the present invention can be produced according to the method for producing a photosensitive transfer material described in paragraphs 0094 to 0098 of JP-A-2006-259138. Among them, the transfer film of the present invention is preferably manufactured by the following transfer film manufacturing method of the present invention.

The transfer film manufacturing method of the present invention includes a step of forming a first curable transparent resin layer on a temporary support, and a second curable transparent resin layer directly on the first curable transparent resin layer. And forming either one of the first curable transparent resin layer and the second curable transparent resin layer with a water / alcohol content of 1 to 3 carbon atoms in a mass ratio of 58 /. A coating solution containing 42 to 100/0 water or a mixed solvent is applied and the other is formed by applying a coating solution containing an organic solvent, and the refractive index of the second curable transparent resin layer is the first. It is higher than the refractive index of one curable transparent resin layer, and the refractive index of the second curable transparent resin layer is 1.6 or more.
With such a configuration, the interface between the first curable transparent resin layer and the second curable resin layer described above can be clarified to further improve the visibility of the transparent electrode pattern. In addition, any one of the first and second curable transparent resin layers is a coating solution containing water or a mixed solvent of water having an alcohol content of 1 to 3 carbon atoms in a mass ratio of 58/42 to 100/0. And forming the second curable transparent resin layer without curing after laminating the first curable transparent resin layer by forming a coating liquid containing an organic solvent on the other side. Even when laminated, the layer fraction is good and the visibility of the transparent electrode pattern can be improved, and the refractive index adjusting layer (ie, the first and second curable transparent resin layers) is transferred from the transfer film to the transparent electrode pattern. After being transferred onto, it can be developed into a desired pattern by photolithography.

  The method for producing a transfer film of the present invention preferably includes a step of further forming a thermoplastic resin layer before forming the first curable transparent resin layer on the temporary support.

  The method for producing a transfer film of the present invention comprises a step of forming an intermediate layer between the thermoplastic resin layer and the first curable transparent resin layer after the step of forming the thermoplastic resin layer. It is preferable to include. When the above-mentioned photosensitive film having an intermediate layer is specifically formed, a solution (thermoplastic resin coating solution) in which an additive is dissolved together with a thermoplastic organic polymer is applied on a temporary support. After drying and providing a thermoplastic resin layer, a preparation liquid (intermediate layer coating liquid) prepared by adding a resin or an additive to a solvent that does not dissolve the thermoplastic resin layer is applied onto the thermoplastic resin layer. Then, the intermediate layer is laminated by drying, and a colored photosensitive resin layer coating solution prepared using a solvent that does not dissolve the intermediate layer is further applied onto the intermediate layer and dried to form a colored photosensitive resin layer. By stacking, it can be suitably produced.

[Transparent laminate]
The transparent laminate of the present invention is produced by the method for producing a transparent laminate of the present invention. The transparent electrode pattern, the second curable transparent resin layer disposed adjacent to the transparent electrode pattern, and the second A first curable transparent resin layer disposed adjacent to the curable transparent resin layer, and the refractive index of the second curable transparent resin layer is the same as that of the first curable transparent resin layer. It is preferable that the refractive index of the second curable transparent resin layer is higher than the refractive index and 1.6 or more.
By setting it as such a structure, the problem that a transparent electrode pattern is visually recognized can be solved, and patterning property becomes favorable.
Furthermore, it is preferable that the transparent laminated body of the present invention is well colored, that is, not yellowish. Moreover, it is preferable that the transparent laminated body of this invention has favorable board | substrate adhesiveness.

<Configuration of transparent laminate>
The transparent laminate of the present invention has a refractive index of 1.6 to 1.78 and a film thickness of 55 on the side of the transparent electrode pattern opposite to the side on which the second curable transparent resin layer is formed. It is preferable to further have a transparent film of ˜110 nm from the viewpoint of further improving the visibility of the transparent electrode pattern. In the present specification, when “transparent film” is described without particular notice, it refers to the “transparent film having a refractive index of 1.6 to 1.78 and a film thickness of 55 to 110 nm”.
The transparent laminate of the present invention has a transparent substrate on the opposite side of the transparent film having the refractive index of 1.6 to 1.78 and a film thickness of 55 to 110 nm on which the transparent electrode pattern is formed. Furthermore, it is preferable to have.

FIG. 11 shows an example of the configuration of the transparent laminate of the present invention.
In FIG. 11, the transparent substrate 1 has a transparent film 11 having a refractive index of 1.6 to 1.78 and a film thickness of 55 to 110 nm, and further includes a transparent electrode pattern 4, a second curable transparent resin layer 12, and The first curable transparent resin layer 7 has an area 21 in which the first curable transparent resin layer 7 is laminated in this order. In addition, in FIG. 11, in addition to the above-described region, the transparent laminate described above is a region in which a transparent substrate 1 and a multilayer film 11 including at least two kinds of transparent thin films having different refractive indexes are laminated in this order (FIG. 11). In the configuration, the region includes the region 22 in which the second curable transparent resin layer 12 and the first curable transparent resin layer 7 are laminated in this order (that is, the non-pattern region 22 where the transparent electrode pattern is not formed). It has been shown.
In other words, the substrate with a transparent electrode pattern described above includes the transparent substrate 1, the multilayer film 11 including at least two kinds of transparent thin films having different refractive indexes, the transparent electrode pattern 4, the second curable transparent resin layer 12, and the first substrate. A region 21 in which one curable transparent resin layer 7 is laminated in this order is included in the in-plane direction.
The in-plane direction means a direction substantially parallel to a plane parallel to the transparent substrate of the transparent laminate. Therefore, the transparent electrode pattern 4, the second curable transparent resin layer 12, and the first curable transparent resin layer 7 include in the plane a region in which the transparent electrode pattern 4, the second curable transparent resin layer 12 and the first curable transparent resin layer 7 are laminated in this order. The orthogonal projection of the region where the transparent transparent resin layer 12 and the first curable transparent resin layer 7 are laminated in this order onto the plane parallel to the transparent substrate of the transparent laminate is parallel to the transparent substrate of the transparent laminate It means to exist within.
Here, when the transparent laminate of the present invention is used in a capacitance-type input device to be described later, the transparent electrode pattern has a first transparent electrode pattern and a second transparent electrode in two directions substantially orthogonal to the row direction and the column direction, respectively. It may be provided as a transparent electrode pattern (see, for example, FIG. 3). For example, in the configuration of FIG. 3, the transparent electrode pattern in the transparent laminate of the present invention may be the second transparent electrode pattern 4 or the pad portion 3 a of the first transparent electrode pattern 3. In other words, in the following description of the transparent laminate of the present invention, the reference numeral of the transparent electrode pattern may be represented by “4”. However, the transparent electrode pattern in the transparent laminate of the present invention is the static electrode of the present invention. It is not limited to the use for the second transparent electrode pattern 4 in the capacitive input device, but may be used as the pad portion 3a of the first transparent electrode pattern 3, for example.

It is preferable that the transparent laminated body of this invention contains the non-pattern area | region in which the above-mentioned transparent electrode pattern is not formed. In the present specification, the non-pattern region means a region where the transparent electrode pattern 4 is not formed.
FIG. 11 shows an embodiment in which the transparent laminate of the present invention includes a non-pattern region 22.
In the transparent laminate of the present invention, the transparent substrate, the transparent film, and the second curable transparent resin layer described above are formed on at least a part of the non-pattern region 22 where the transparent electrode pattern is not formed. It is preferable to include the area | region laminated | stacked in order in the surface.
In the transparent laminate of the present invention, the transparent film, the second transparent curable transparent resin layer, and the second curable transparent resin layer described above are laminated in this order. The resin layers are preferably adjacent to each other.
However, in the other areas of the non-pattern area 22 described above, other members may be disposed at arbitrary positions as long as they do not contradict the spirit of the present invention. When used in a capacitive input device, the mask layer 2, the insulating layer 5, the conductive element 6 and the like in FIG. 1A can be stacked.

In the transparent laminate of the present invention, the aforementioned transparent substrate and transparent film are preferably adjacent to each other.
FIG. 11 shows a mode in which the above-described transparent film 11 is laminated adjacently on the above-described transparent substrate 1.
However, a third transparent film may be laminated between the above-mentioned transparent substrate and the above-described transparent film as long as it does not contradict the gist of the present invention. For example, it is preferable to include a third transparent film (not shown in FIG. 11) having a refractive index of 1.5 to 1.52 between the transparent substrate and the transparent film.

In the transparent laminate of the present invention, the transparent film preferably has a thickness of 55 to 110 nm, more preferably 60 to 110 nm, and particularly preferably 70 to 90 nm.
Here, the transparent film described above may have a single layer structure or a laminated structure of two or more layers. When the above-mentioned transparent film has a laminated structure of two or more layers, the film thickness of the above-mentioned transparent film means the total film thickness of all layers.

In the transparent laminate of the present invention, the transparent film and the transparent electrode pattern are preferably adjacent to each other.
FIG. 11 shows an aspect in which the transparent electrode pattern 4 is laminated adjacently on a partial region of the transparent film 11.
As shown in FIG. 11, the end portion of the transparent electrode pattern 4 is not particularly limited in shape, but may have a tapered shape. For example, the surface on the transparent substrate side described above is the above-described surface. It may have a taper shape wider than the surface opposite to the transparent substrate.
Here, the angle of the end portion of the transparent electrode pattern (hereinafter also referred to as a taper angle) when the end portion of the transparent electrode pattern has a tapered shape is preferably 30 ° or less, 0.1 to 15 More preferably, it is 0.5 to 5 °.
The method for measuring the taper angle in this specification can be obtained by taking a photomicrograph of the end of the transparent electrode pattern described above, approximating the taper portion of the photomicrograph to a triangle, and directly measuring the taper angle. .
FIG. 10 shows an example in which the end portion of the transparent electrode pattern is tapered. The triangle that approximates the tapered portion in FIG. 10 has a bottom surface of 800 nm and a height (film thickness at the upper base portion substantially parallel to the bottom surface) of 40 nm, and the taper angle α at this time is about 3 °. The triangular bottom surface approximating the tapered portion is preferably 10 to 3000 nm, more preferably 100 to 1500 nm, and particularly preferably 300 to 1000 nm.
In addition, the preferable range of the height of the triangle which approximated the taper part is the same as the preferable range of the film thickness of the transparent electrode pattern.

The transparent laminate of the present invention preferably includes a region where the above-mentioned transparent electrode pattern and the above-mentioned second curable transparent resin layer are adjacent to each other.
FIG. 11 shows the above-mentioned transparent electrode pattern, the above-mentioned transparent electrode pattern, the above-mentioned second curable transparent resin layer, and the above-mentioned transparent electrode pattern, the above-mentioned second curable transparent resin layer, A mode in which the curable transparent resin layer and the first curable transparent resin layer are adjacent to each other is shown.

Further, the transparent laminate of the present invention has both the transparent electrode pattern and the non-pattern region 22 where the transparent electrode pattern is not formed by the transparent film and the second curable transparent resin layer. It is preferably coated directly or via other layers.
Here, “continuously” means that the transparent film and the second curable transparent resin layer are not a pattern film but a continuous film. That is, the above-mentioned transparent film and the above-mentioned second curable transparent resin layer preferably have no opening from the viewpoint of making the transparent electrode pattern difficult to be visually recognized.
In addition, the transparent electrode pattern and the non-pattern region 22 described above are directly covered with the transparent film and the second curable transparent resin layer described above rather than being covered with another layer. Is preferred. As the “other layer” in the case of being covered through another layer, the insulating layer 5 included in the capacitive input device of the present invention described later, or the capacitive input device of the present invention described later is used. Thus, when two or more layers of transparent electrode patterns are included, a second layer of transparent electrode patterns can be exemplified.
FIG. 11 shows an aspect in which the second curable transparent resin layer 12 is laminated. The second curable transparent resin layer 12 described above is laminated over the region where the transparent electrode pattern 4 on the transparent film 11 is not stacked and the region where the transparent electrode pattern 4 is stacked. ing. That is, the aforementioned second curable transparent resin layer 12 is adjacent to the aforementioned transparent film 11, and further, the aforementioned second curable transparent resin layer 12 is adjacent to the transparent electrode pattern 4. .
Moreover, when the edge part of the transparent electrode pattern 4 is a taper shape, it is preferable that the above-mentioned 2nd curable transparent resin layer 12 is laminated | stacked along the taper shape (with the same inclination as a taper angle).

  In FIG. 11, the first curable transparent resin layer 7 is laminated on the surface of the second curable transparent resin layer 12 opposite to the surface on which the transparent electrode pattern is formed. It is shown.

<Material of transparent laminate>
(Transparent substrate)
In the transparent laminate of the present invention, the above-mentioned transparent substrate is preferably a glass substrate having a refractive index of 1.5 to 1.55. The refractive index of the transparent substrate is particularly preferably 1.5 to 1.52.
The transparent substrate described above is composed of a light-transmitting substrate such as a glass substrate, and tempered glass represented by Corning's gorilla glass can be used. Moreover, as the above-mentioned transparent substrate, the materials used in JP 2010-86684 A, JP 2010-152809 A, and JP 2010-257492 A can be preferably used.

(Transparent electrode pattern)
The refractive index of the transparent electrode pattern is preferably 1.75 to 2.1.
The material for the transparent electrode pattern is not particularly limited, and a known material can be used. For example, it can be made of a light-transmitting conductive metal oxide film such as ITO (Indium Tin Oxide) or IZO (Indium Zinc Oxide). Examples of such a metal film include an ITO film; a metal film such as Al, Zn, Cu, Fe, Ni, Cr, and Mo; a metal oxide film such as SiO 2. At this time, the film thickness of each element can be 10 to 200 nm. Further, since the amorphous ITO film is made into a polycrystalline ITO film by firing, the electrical resistance can be reduced. The first transparent electrode pattern 3, the second transparent electrode pattern 4, and the conductive element 6 described later are a photosensitive film having a photocurable resin layer using the conductive fibers described above. It can also be manufactured. In addition, when the first conductive pattern or the like is formed of ITO or the like, paragraphs 0014 to 0016 of Japanese Patent No. 4506785 can be referred to. Among these, the transparent electrode pattern described above is preferably an ITO film.
The transparent laminate of the present invention is preferably an ITO film having a refractive index of 1.75 to 2.1.

(First curable transparent resin layer and second curable transparent resin layer)
The preferred ranges of the first curable transparent resin layer and the second curable transparent resin layer contained in the transparent laminate of the present invention are the above-described first curable transparent resin layer and the above-described range in the transfer film of the present invention. This is the same as the preferred range of the second curable transparent resin layer.

(Transparent film)
In the transparent laminate of the present invention, the refractive index of the transparent film is 1.6 to 1.78, and preferably 1.65 to 1.74. Here, the transparent film described above may have a single layer structure or a laminated structure of two or more layers. When the aforementioned transparent film has a laminated structure of two or more layers, the refractive index of the aforementioned transparent film means the refractive index of all layers.
As long as the refractive index range is satisfied, the material for the transparent film is not particularly limited.

The preferred range of the material for the transparent film and the preferred range for the physical properties such as refractive index are the same as those for the second curable transparent resin layer.
In the transparent laminate of the present invention, it is preferable from the viewpoint of optical homogeneity that the transparent film and the second curable transparent resin layer are made of the same material.

In the transparent laminate of the present invention, the above-mentioned transparent film is preferably a transparent resin film.
The metal oxide particles, resin (binder) and other additives used for the transparent resin film are not particularly limited as long as they do not contradict the gist of the present invention, and the second curable transparent film described above in the transfer film of the present invention. Resins used for the resin layer and other additives can be preferably used.
In the transparent laminate of the present invention, the transparent film may be an inorganic film. As a material used for the inorganic film, a material used for the above-mentioned second curable transparent resin layer in the transfer film of the present invention can be preferably used.

(Third transparent film)
The refractive index of the above-mentioned third transparent film is preferably 1.5 to 1.55 from the viewpoint of improving the visibility of the transparent electrode pattern by approaching the refractive index of the above-mentioned transparent substrate, More preferably, it is -1.52.

[Method for producing transparent laminate]
In the method for producing a transparent laminate of the present invention, the above-described second curable transparent resin layer and the above-mentioned first curable transparent resin layer of the transfer film of the present invention are laminated in this order on the transparent electrode pattern. Including a process.
With such a configuration, the second curable transparent resin layer of the transparent laminate and the first curable transparent resin layer described above can be collectively transferred, and there is no problem that the transparent electrode pattern is visually recognized. The laminate can be easily manufactured with high productivity.
In the method for producing a transparent laminate of the present invention, the second curable transparent resin layer is directly on the transparent electrode pattern and on the transparent film in the non-pattern region, A film is formed through the layers.

(Surface treatment of transparent substrate)
Moreover, in order to improve the adhesiveness of each layer by the lamination in a subsequent transfer process, a surface treatment can be performed on the non-contact surface of the transparent substrate (front plate) in advance. As the aforementioned surface treatment, it is preferable to carry out a surface treatment (silane coupling treatment) using a silane compound. As the silane coupling agent, those having a functional group that interacts with the photosensitive resin are preferable. For example, a silane coupling solution (N-β (aminoethyl) γ-aminopropyltrimethoxysilane) 0.3 mass% aqueous solution, trade name: KBM603, manufactured by Shin-Etsu Chemical Co., Ltd.) is sprayed for 20 seconds with a shower, and a pure water shower Wash. Thereafter, the reaction is carried out by heating. A heating tank may be used, and the reaction can be promoted by preheating the substrate of the laminator.

(Transparent electrode pattern film formation)
The above-mentioned transparent electrode pattern uses the method of forming the first transparent electrode pattern 3, the second transparent electrode pattern 4, and another conductive element 6 in the description of the capacitive input device of the present invention described later. Thus, it is possible to form a film on a transparent substrate or a transparent film having a refractive index of 1.6 to 1.78 and a film thickness of 55 to 110 nm, and a method using a photosensitive film is preferable.

(Film formation of the first curable transparent resin layer and the second curable transparent resin layer)
The method for forming the first curable transparent resin layer and the second curable transparent resin layer described above includes a protective film removing step for removing the protective film from the transfer film of the present invention, and the protective film described above. The transfer step of transferring the first curable transparent resin layer and the second curable transparent resin layer of the transfer film of the present invention from which the film has been removed onto the transparent electrode pattern, and transferred onto the transparent electrode pattern An exposure step of exposing the first curable transparent resin layer and the second curable transparent resin layer, and the exposed first curable transparent resin layer and the second curable transparent resin layer. And a developing step of developing.

-Transfer process-
The transfer step described above is a step of transferring the first curable transparent resin layer and the second curable transparent resin layer of the transfer film of the present invention from which the protective film has been removed onto the transparent electrode pattern. It is.
At this time, a method including a step of removing the temporary support after laminating the first curable transparent resin layer and the second curable transparent resin layer of the transfer film of the present invention on the transparent electrode pattern is preferable.
The transfer (bonding) of the first curable transparent resin layer and the second curable transparent resin layer to the substrate surface is performed by the first curable transparent resin layer and the second curable transparent resin layer. The curable transparent resin layer is placed on the surface of the transparent electrode pattern, and is pressurized and heated. For laminating, known laminators such as a laminator, a vacuum laminator, and an auto-cut laminator that can further increase productivity can be used.

-Exposure process, development process, and other processes-
As examples of the exposure step, the development step, and other steps described above, the method described in paragraphs 0035 to 0051 of JP-A-2006-23696 can be suitably used in the present invention.

The exposure process is a process of exposing the first curable transparent resin layer and the second curable transparent resin layer transferred onto the transparent electrode pattern.
Specifically, a predetermined mask is disposed above the first curable transparent resin layer and the second curable transparent resin layer formed on the transparent electrode pattern, and then the mask, The method of exposing the above-mentioned 1st curable transparent resin layer and the above-mentioned 2nd curable transparent resin layer from a mask upper direction through a temporary support body is mentioned.
Here, as a light source for the exposure, light having a wavelength range that can cure the first curable transparent resin layer and the second curable transparent resin layer is irradiated (for example, 365 nm, 405 nm, etc.). If possible, it can be selected and used as appropriate. Specifically, an ultrahigh pressure mercury lamp, a high pressure mercury lamp, a metal halide lamp, etc. are mentioned. As an exposure amount, it is about 5-200 mJ / cm < ² > normally, Preferably it is about 10-100 mJ / cm < ² >.

The aforementioned developing process is a process of developing the exposed photocurable resin layer.
In the present invention, the above-described developing step is a developing step in a narrow sense in which the pattern-exposed first curable transparent resin layer and the second curable transparent resin layer are subjected to pattern development with a developer. .
The development described above can be performed using a developer. The developer is not particularly limited, and a known developer such as the developer described in JP-A-5-72724 can be used. The developing solution is preferably a developing solution in which the photocurable resin layer has a dissolution type developing behavior. For example, a developing solution containing a compound having pKa = 7 to 13 at a concentration of 0.05 to 5 mol / L is preferable. On the other hand, the developer in the case where the first curable transparent resin layer and the second curable transparent resin layer itself do not form a pattern does not dissolve the non-alkali development type coloring composition layer. A developing solution that behaves is preferable. For example, a developing solution containing a compound having a pKa of 7 to 13 at a concentration of 0.05 to 5 mol / L is preferable. A small amount of an organic solvent miscible with water may be added to the developer. Examples of organic solvents miscible with water include methanol, ethanol, 2-propanol, 1-propanol, butanol, diacetone alcohol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol mono-n-butyl ether, and benzyl alcohol. , Acetone, methyl ethyl ketone, cyclohexanone, ε-caprolactone, γ-butyrolactone, dimethylformamide, dimethylacetamide, hexamethylphosphoramide, ethyl lactate, methyl lactate, ε-caprolactam, N-methylpyrrolidone and the like. The concentration of the organic solvent is preferably 0.1% by mass to 30% by mass.
Further, a known surfactant can be further added to the developer. The concentration of the surfactant is preferably 0.01% by mass to 10% by mass.

  As the development method described above, any of paddle development, shower development, shower & spin development, dip development, and the like may be used. Here, the above-described shower development will be described. The uncured portion is removed by spraying a developer onto the first curable transparent resin layer and the second curable transparent resin layer after exposure. can do. When a thermoplastic resin layer or an intermediate layer is provided, an alkaline solution having a low solubility of the photocurable resin layer is sprayed by a shower or the like before development to remove the thermoplastic resin layer or the intermediate layer. It is preferable to keep it. Further, after the development, it is preferable to remove the development residue while spraying a cleaning agent or the like with a shower and rubbing with a brush or the like. The liquid temperature of the developer is preferably 20 ° C. to 40 ° C., and the pH of the developer is preferably 8 to 13.

  The above-described method for manufacturing a capacitive input device may have other steps such as a post-exposure step and a post-bake step. When the first curable transparent resin layer and the second curable transparent resin layer are thermosetting transparent resin layers, it is preferable to perform a post-bake process.

  The patterning exposure and the entire surface exposure may be performed after peeling the temporary support, or may be performed before peeling the temporary support, and then the temporary support may be peeled off. Exposure through a mask or digital exposure using a laser or the like may be used.

(Transparent film formation)
The transparent laminate of the present invention has a refractive index of 1.6 to 1.78 and a film thickness of 55 on the opposite side of the transparent electrode pattern on which the second curable transparent resin layer is formed. When it further has a transparent film of ˜110 nm, the aforementioned transparent film is formed directly on the aforementioned transparent electrode pattern or through another layer such as the aforementioned third transparent film.
The method for forming the transparent film is not particularly limited, but is preferably formed by transfer or sputtering.
Among them, the transparent laminate of the present invention is preferably formed by transferring the transparent curable resin film formed on the temporary support onto the transparent substrate as described above, More preferably, the film is cured after transfer to form a film. As a method of transfer and curing, the photosensitive film in the description of the capacitance-type input device of the present invention to be described later is used, the first curable transparent resin layer described above in the method for producing the transparent laminate of the present invention, In the same manner as the method of transferring the second curable transparent resin layer, a method of performing transfer, exposure, development and other steps can be mentioned. In that case, it is preferable to adjust the refractive index of the transparent film in the above range by dispersing the metal oxide particles in the photocurable resin layer in the photosensitive film.

On the other hand, when the transparent film is an inorganic film, it is preferably formed by sputtering. That is, it is also preferable that the transparent laminate of the present invention is formed by sputtering the above-described transparent film.
As the sputtering method, the methods used in JP 2010-86684 A, JP 2010-152809 A, and JP 2010-257492 A can be preferably used.

(Third transparent film formation)
The third transparent film forming method is the same as the method of forming a transparent film having a refractive index of 1.6 to 1.78 and a film thickness of 55 to 110 nm on a transparent substrate.

[Method for producing transparent laminate]
The manufacturing method of the transparent laminated body of this invention includes the process of laminating | stacking the 2nd curable transparent resin layer and 1st curable transparent resin layer of the transfer film of this invention in this order on a transparent electrode pattern.

The method for producing a transparent laminate of the present invention preferably includes a step of simultaneously curing the first curable transparent resin layer and the second curable transparent resin layer, and more preferably includes a step of pattern curing at the same time. . In the transfer film of the present invention, after the first curable transparent resin layer is laminated, the second curable transparent resin layer is preferably laminated without curing the first curable transparent resin layer. The first curable transparent resin layer and the second curable transparent resin layer transferred from the transfer film of the present invention thus obtained can be simultaneously cured. Thereby, after transferring the first and second curable transparent resin layers from the transfer film of the present invention onto the transparent electrode pattern, it can be developed into a desired pattern by photolithography.
In the method for producing a transparent laminate of the present invention, the first curable transparent resin layer and the second curable resin are cured after the step of simultaneously curing the first curable transparent resin layer and the second curable transparent resin layer. It is more preferable to include a step of developing and removing an uncured portion of the transparent resin layer (in the case of photocuring, only the unexposed portion or only the exposed portion).

[Capacitance type input device]
The capacitance-type input device of the present invention is produced using the transfer film of the present invention, or has the transparent laminate of the present invention.
The capacitance-type input device of the present invention includes a first curable transparent resin disposed adjacent to the second curable transparent resin layer and the second curable transparent resin layer from the transfer film of the present invention. The layer is preferably produced by transferring the layer onto the transparent electrode pattern of the capacitive input device.
The capacitance-type input device of the present invention is preferably formed by simultaneously curing the first curable transparent resin layer and the second curable transparent resin layer transferred from the transfer film of the present invention. More preferably, the curable transparent resin layer and the second curable transparent resin layer are subjected to pattern curing at the same time. In addition, when simultaneously hardening | curing the 1st curable transparent resin layer and the 2nd curable transparent resin layer which were transcribe | transferred from the transfer film of this invention, it is preferable not to peel a protective film from the transfer film of this invention.
The capacitance-type input device of the present invention develops uncured portions of the first curable transparent resin layer and the second curable transparent resin layer which are transferred from the transfer film of the present invention and simultaneously pattern-cured. More preferably, it is removed. In addition, after simultaneously curing the first curable transparent resin layer and the second curable transparent resin layer transferred from the transfer film of the present invention, the protective film is peeled off from the transfer film of the present invention before development. Is preferred. Since the capacitance-type input device of the present invention needs to be connected to the flexible wiring formed on the polyimide film at the terminal portion of the routing wiring, the first curable transparent resin layer (and the second curable property) It is preferably not covered with a transparent resin layer.
This aspect is shown in FIG. FIG. 13 shows a capacitance-type input device having the following configuration including a lead wire (another conductive element 6) of a transparent electrode pattern and a terminal portion 31 of the lead wire.
Since the first curable transparent resin layer (and the second curable transparent resin layer) on the terminal portion 31 of the routing wiring is an uncured portion (unexposed portion), it is removed by development, and the routing wiring The terminal unit 31 is exposed.
Specific exposure and development modes are shown in FIGS. FIG. 14 shows a state in which a transfer film 30 of the present invention having first and second curable transparent resin layers is laminated on a transparent electrode pattern of a capacitance type input device by lamination and cured by exposure or the like. Indicates the state. When using photolithography, that is, when cured by exposure, the cured portion (exposed portion) 33 of the first curable transparent resin layer and the second curable transparent resin layer having the shape shown in FIG. 15 is masked. Can be obtained by pattern exposure and development of an unexposed portion using. Specifically, in FIG. 15, the opening 34 corresponding to the terminal portion of the routing wiring as the uncured portion of the first curable transparent resin layer and the second curable transparent resin layer, and the capacitive input device The end portion of the lead-out wiring (extraction wiring portion) from which the end portions of the transfer film of the present invention having the first and second curable transparent resin layers protruding outside the outline of the frame portion of the present invention are removed is covered. Therefore, a cured portion (desired pattern) of the first and second curable transparent resin layers is obtained.
Thereby, the flexible wiring produced on the polyimide film can be directly connected to the terminal portion 31 of the routing wiring, and the sensor signal can be sent to the electric circuit.
The capacitance-type input device of the present invention includes a transparent electrode pattern, a second curable transparent resin layer disposed adjacent to the transparent electrode pattern, and the second curable transparent resin layer. A refractive index of the second curable transparent resin layer is higher than a refractive index of the first curable transparent resin layer, and the first curable transparent resin layer is disposed. It is preferable to have a transparent laminate in which the refractive index of the second curable transparent resin layer is 1.6 or more.
Hereinafter, the detail of the preferable aspect of the electrostatic capacitance type input device of this invention is demonstrated.

The capacitance type input device of the present invention includes at least the following (3) to (5) on the front plate (corresponding to the transparent substrate in the transparent laminate of the present invention) and the non-contact surface side of the front plate. , (7) and (8), and preferably has the transparent laminate of the present invention.
(3) A plurality of first transparent electrode patterns formed by extending a plurality of pad portions in the first direction via the connection portions;
(4) A plurality of second electrode patterns comprising a plurality of pad portions that are electrically insulated from the first transparent electrode pattern and extend in a direction intersecting the first direction.
(5) An insulating layer for electrically insulating the first transparent electrode pattern and the second electrode pattern described above;
(7) a second curable transparent resin layer formed so as to cover all or part of the elements of (3) to (5) described above;
(8) The 1st curable transparent resin layer formed adjacently so that the element of above-mentioned (7) might be covered.
Here, the above-mentioned (7) second curable transparent resin layer corresponds to the above-mentioned second curable transparent resin layer in the transparent laminate of the present invention. The above-mentioned (8) first curable transparent resin layer corresponds to the above-mentioned first curable transparent resin layer in the transparent laminate of the present invention. The first curable transparent resin layer described above is preferably a so-called transparent protective layer in a generally known electrostatic capacitance type input device.

In the capacitive input device of the present invention, the above-mentioned (4) second electrode pattern may be a transparent electrode pattern or a transparent electrode pattern, but is preferably a transparent electrode pattern.
The capacitance-type input device of the present invention further includes (6) the first transparent electrode described above that is electrically connected to at least one of the first transparent electrode pattern and the second electrode pattern described above. The conductive element may be different from the pattern and the second electrode pattern described above.
Here, when the above-mentioned (4) second electrode pattern is not a transparent electrode pattern and does not have the above-mentioned (6) another conductive element, the above-mentioned (3) first transparent electrode pattern is It corresponds to the transparent electrode pattern in the transparent laminate of the present invention.
When the above-mentioned (4) second electrode pattern is a transparent electrode pattern and does not have the above-mentioned (6) another conductive element, the above-mentioned (3) first transparent electrode pattern and the above-mentioned (4 ) At least one of the second electrode patterns corresponds to the transparent electrode pattern in the transparent laminate of the present invention.
When the above-mentioned (4) second electrode pattern is not a transparent electrode pattern but has the above-mentioned (6) another conductive element, the above-mentioned (3) the first transparent electrode pattern and the above-mentioned (6) another At least one of the conductive elements corresponds to the transparent electrode pattern in the transparent laminate of the present invention.
When the above-mentioned (4) second electrode pattern is a transparent electrode pattern and has the above-mentioned (6) another conductive element, the above-mentioned (3) first transparent electrode pattern, the above-mentioned (4) first At least one of the two electrode patterns and the above-described another conductive element (6) corresponds to the transparent electrode pattern in the transparent laminate of the present invention.

  The capacitance-type input device of the present invention further comprises (2) a transparent film, (3) the first transparent electrode pattern and the front plate, (4) the second electrode pattern and the front surface. It is preferable to have between board | substrates or between the above-mentioned (6) another electroconductive element and the above-mentioned front board. Here, (2) the transparent film described above corresponds to a transparent film having a refractive index of 1.6 to 1.78 and a film thickness of 55 to 110 nm in the transparent laminate of the present invention. From the viewpoint of further improving the visibility.

The capacitance-type input device of the present invention preferably further has (1) a mask layer and / or a decoration layer as necessary. The mask layer described above is provided as a black frame around the area touched by a finger or a touch pen so that the transparent electrode pattern routing wiring cannot be visually recognized from the contact side or is decorated. The above-mentioned decoration layer is provided for decoration as a frame around the area touched with a finger or a touch pen. For example, it is preferable to provide a white decoration layer.
The above-mentioned (1) mask layer and / or decorative layer are the above-mentioned (2) between the transparent film and the above-mentioned front plate, (3) between the above-mentioned (3) first transparent electrode pattern and the above-mentioned front plate, and (4) above-mentioned. It is preferable to have between a 2nd transparent electrode pattern and the above-mentioned front board, or between the above-mentioned (6) another electroconductive element and the above-mentioned front board. The aforementioned (1) mask layer and / or decorative layer is more preferably provided adjacent to the aforementioned front plate.

  Even if the capacitance-type input device of the present invention includes such various members, the second curable transparent resin layer disposed adjacent to the transparent electrode pattern and the first By including the above-mentioned first curable transparent resin layer disposed adjacent to the second curable transparent resin layer, the transparent electrode pattern can be made inconspicuous and the visibility problem of the transparent electrode pattern is improved. can do. Further, as described above, the transparent electrode pattern is sandwiched between the transparent film having the refractive index of 1.6 to 1.78 and the film thickness of 55 to 110 nm and the second curable transparent resin layer. By adopting the configuration, the problem of visibility of the transparent electrode pattern can be further improved.

<Configuration of capacitance type input device>
First, a preferable configuration of the capacitive input device of the present invention will be described together with a method for manufacturing each member constituting the device. FIG. 1A is a cross-sectional view showing a preferred configuration of the capacitive input device of the present invention. In FIG. 1A, a capacitive input device 10 includes a transparent substrate (front plate) 1, a mask layer 2, a transparent film 11 having a refractive index of 1.6 to 1.78 and a film thickness of 55 to 110 nm, A first transparent electrode pattern 3, a second transparent electrode pattern 4, an insulating layer 5, a conductive element 6, a second curable transparent resin layer 12, and a first curable transparent resin layer 7. The aspect comprised from these is shown.
Moreover, FIG. 1B showing the XX ′ cross section in FIG. 3 to be described later is also a cross-sectional view showing a preferable configuration of the capacitive input device of the present invention. 1B, the capacitive input device 10 includes a transparent substrate (front plate) 1, a transparent film 11 having a refractive index of 1.6 to 1.78 and a film thickness of 55 to 110 nm, and a first transparent electrode. The aspect comprised from the pattern 3, the 2nd transparent electrode pattern 4, the 2nd curable transparent resin layer 12, and the 1st curable transparent resin layer 7 is shown.

  For the transparent substrate (front plate) 1, the materials mentioned as the material for the transparent electrode pattern in the transparent laminate of the present invention can be used. Moreover, in FIG. 1A, the side in which each element of the front plate 1 is provided is referred to as a non-contact surface side. In the capacitive input device 10 of the present invention, input is performed by bringing a finger or the like into contact with the contact surface (the surface opposite to the non-contact surface) of the front plate 1.

A mask layer 2 is provided on the non-contact surface of the front plate 1. The mask layer 2 is a frame-shaped pattern around the display area formed on the non-contact surface side of the front panel of the touch panel, and is formed so as not to show the lead wiring and the like.
As shown in FIG. 2, the capacitive input device 10 of the present invention is provided with a mask layer 2 so as to cover a part of the front plate 1 (a region other than the input surface in FIG. 2). Yes. Further, the front plate 1 can be provided with an opening 8 in part as shown in FIG. A pressing mechanical switch can be installed in the opening 8.

  On the contact surface of the front plate 1, a plurality of first transparent electrode patterns 3 formed by extending a plurality of pad portions in the first direction via connection portions; A plurality of second transparent electrode patterns 4 made of a plurality of pad portions that are electrically insulated and extend in a direction intersecting the first direction, the first transparent electrode pattern 3 and the second An insulating layer 5 that electrically insulates the transparent electrode pattern 4 is formed. What was mentioned as the material of the transparent electrode pattern in the transparent laminated body of this invention can be used for the above-mentioned 1st transparent electrode pattern 3, the 2nd transparent electrode pattern 4, and the electroconductive element 6 mentioned later. An ITO film is preferable.

In addition, at least one of the first transparent electrode pattern 3 and the second transparent electrode pattern 4 extends over both the non-contact surface of the front plate 1 and the region of the mask layer 2 opposite to the front plate 1. Can be installed. In FIG. 1A, a diagram is shown in which the second transparent electrode pattern is installed across both areas of the non-contact surface of the front plate 1 and the surface of the mask layer 2 opposite to the front plate 1. Yes.
Thus, even when a photosensitive film is laminated across the mask layer and the back surface of the front plate that require a certain thickness, an expensive film such as a vacuum laminator can be used by using a photosensitive film having a specific layer structure to be described later. Even without the use of equipment, it is possible to perform lamination without generating bubbles at the mask portion boundary with a simple process.

The first transparent electrode pattern 3 and the second transparent electrode pattern 4 will be described with reference to FIG. FIG. 3 is an explanatory diagram showing an example of the first transparent electrode pattern and the second transparent electrode pattern in the present invention. As shown in FIG. 3, the first transparent electrode pattern 3 is formed such that the pad portion 3a extends in the first direction via the connection portion 3b. The second transparent electrode pattern 4 is electrically insulated by the first transparent electrode pattern 3 and the insulating layer 5 and extends in a direction intersecting the first direction (second direction in FIG. 3). It is constituted by a plurality of pad portions that are formed. Here, when the first transparent electrode pattern 3 is formed, the pad portion 3a and the connection portion 3b described above may be manufactured as one body, or only the connection portion 3b is manufactured, and the pad portion 3a and the second portion 3b are formed. The transparent electrode pattern 4 may be integrally formed (patterned). When the pad portion 3a and the second transparent electrode pattern 4 are produced (patterned) as a single body (patterning), as shown in FIG. 3, a part of the connection part 3b and a part of the pad part 3a are connected, and an insulating layer is formed. Each layer is formed so that the first transparent electrode pattern 3 and the second transparent electrode pattern 4 are electrically insulated by 5.
Moreover, the area | region in which the 1st transparent electrode pattern 3 in FIG. 3, the 2nd transparent electrode pattern 4, and the electroconductive element 6 mentioned later is not formed is equivalent to the non-pattern area | region 22 in the transparent laminated body of this invention.

In FIG. 1A, a conductive element 6 is provided on the side of the mask layer 2 opposite to the front plate 1. The conductive element 6 is electrically connected to at least one of the first transparent electrode pattern 3 and the second transparent electrode pattern 4, and is different from the first transparent electrode pattern 3 and the second transparent electrode pattern 4. Is another element.
In FIG. 1A, a view in which the conductive element 6 is connected to the second transparent electrode pattern 4 is shown.

  Moreover, in FIG. 1A, the 1st curable transparent resin layer 7 is installed so that all of each component may be covered. The 1st curable transparent resin layer 7 may be comprised so that only a part of each component may be covered. The insulating layer 5 and the first curable transparent resin layer 7 may be the same material or different materials. As a material which comprises the insulating layer 5, what was mentioned as a material of the 1st or 2nd curable transparent resin layer in the transparent laminated body of this invention can be used preferably.

<Method for Manufacturing Capacitive Input Device>
Examples of the embodiment formed in the process of manufacturing the capacitive input device of the present invention include the embodiments shown in FIGS. FIG. 4 is a top view illustrating an example of the tempered glass 11 in which the opening 8 is formed. FIG. 5 is a top view showing an example of the front plate on which the mask layer 2 is formed. FIG. 6 is a top view showing an example of the front plate on which the first transparent electrode pattern 3 is formed. FIG. 7 is a top view showing an example of a front plate on which the first transparent electrode pattern 3 and the second transparent electrode pattern 4 are formed. FIG. 8 is a top view showing an example of a front plate on which conductive elements 6 different from the first and second transparent electrode patterns are formed. These show the example which actualized the following description, and the scope of the present invention is not limitedly interpreted by these drawings.

  In the method of manufacturing a capacitance-type input device, when the second curable transparent resin layer 12 and the first curable transparent resin layer 7 are formed, each element is formed using the transfer film of the present invention. Can be formed by transferring the above-mentioned second curable transparent resin layer and the above-mentioned first curable transparent resin layer to the surface of the above-mentioned front plate 1 formed arbitrarily.

In the method for manufacturing the capacitance type input device, at least one element of the mask layer 2, the first transparent electrode pattern 3, the second transparent electrode pattern 4, the insulating layer 5, and the conductive element 6 is: It is preferable to form using the above-mentioned photosensitive film which has a temporary support body and a photocurable resin layer in this order.
When each of the above-described elements is formed using the transfer film of the present invention or the above-described photosensitive film, there is no resist component leakage from the opening even on the substrate having the opening (front plate), and particularly up to the boundary line of the front plate. In the mask layer that needs to form a light-shielding pattern, there is no protrusion of the resist component from the glass edge, so there is no contamination of the back side of the front plate. Can be manufactured.

  Using the above-mentioned photosensitive film as a permanent material such as the first transparent electrode pattern, the second transparent electrode pattern and the conductive element when the mask layer, the insulating layer, and the conductive photocurable resin layer are used. The photosensitive film is laminated to the substrate and then exposed in a pattern as necessary. In the case of negative materials, the unexposed portion is exposed, and in the case of positive materials, the exposed portion is developed. The pattern can be obtained by removing them. In the development, the thermoplastic resin layer and the photocurable resin layer may be developed and removed with separate liquids, or may be removed with the same liquid. You may combine well-known image development facilities, such as a brush and a high pressure jet, as needed. After the development, post-exposure and post-bake may be performed as necessary.

(Photosensitive film)
The above-described photosensitive film other than the transfer film of the present invention, which is preferably used when manufacturing the capacitive input device of the present invention, will be described. The aforementioned photosensitive film preferably has a temporary support and a photocurable resin layer, and preferably has a thermoplastic resin layer between the temporary support and the photocurable resin layer. When a mask layer or the like is formed using the photosensitive film having the thermoplastic resin layer described above, bubbles are less likely to be generated in an element formed by transferring the photocurable resin layer, and image unevenness or the like may occur in the image display device. It is less likely to occur and excellent display characteristics can be obtained.
The aforementioned photosensitive film may be a negative type material or a positive type material.

-Layers other than the photocurable resin layer, production method-
As the above-mentioned temporary support and the above-mentioned thermoplastic resin layer in the above-mentioned photosensitive film, the same thermoplastic resin layer as that used for the transfer film of the present invention can be used. Further, as the method for producing the above-mentioned photosensitive film, the same method as the method for producing the transfer film of the present invention can be used.

-Photocurable resin layer-
The above-mentioned photosensitive film adds an additive to a photocurable resin layer according to the use. That is, when the above-mentioned photosensitive film is used for forming the mask layer, a colorant is contained in the photocurable resin layer. Moreover, when the above-mentioned photosensitive film has an electroconductive photocurable resin layer, electroconductive fiber etc. contain in the above-mentioned photocurable resin layer.

  When the above-mentioned photosensitive film is a negative material, the photocurable resin layer preferably contains an alkali-soluble resin, a polymerizable compound, a polymerization initiator, or a polymerization initiation system. Furthermore, although a conductive fiber, a coloring agent, other additives, etc. are used, it is not restricted to this.

--Alkali-soluble resin, polymerizable compound, the aforementioned polymerization initiator or polymerization initiation system--
As the alkali-soluble resin, the polymerizable compound, the polymerization initiator or the polymerization initiation system contained in the above-described photosensitive film, the same alkali-soluble resin, polymerizable compound, and polymerization initiation as those used in the transfer film of the present invention are used. An agent or a polymerization initiation system can be used.

--Conductive fiber (when used as conductive photocurable resin layer)-
When the above-mentioned photosensitive film laminated with the above-mentioned conductive photocurable resin layer is used for forming a transparent electrode pattern or another conductive element, the following conductive fibers are used for the photocurable resin layer. be able to.

There is no restriction | limiting in particular as a structure of an electroconductive fiber, Although it can select suitably according to the objective, Either a solid structure or a hollow structure is preferable.
Here, the fiber having a solid structure may be referred to as “wire”, and the fiber having a hollow structure may be referred to as “tube”. In addition, a conductive fiber having an average minor axis length of 1 nm to 1,000 nm and an average major axis length of 1 μm to 100 μm may be referred to as “nanowire”.
In addition, conductive fibers having an average minor axis length of 1 nm to 1,000 nm, an average major axis length of 0.1 μm to 1,000 μm, and having a hollow structure may be referred to as “nanotubes”.
The conductive fiber material is not particularly limited as long as it has conductivity, and can be appropriately selected according to the purpose. However, at least one of metal and carbon is preferable, and among these, The conductive fiber is particularly preferably at least one of metal nanowires, metal nanotubes, and carbon nanotubes.

  There is no restriction | limiting in particular as a material of the above-mentioned metal nanowire, For example, the at least 1 sort (s) of metal chosen from the group which consists of a 4th period, a 5th period, and a 6th period of a long periodic table (IUPAC1991) is preferable. More preferably, at least one metal selected from Group 2 to Group 14 is selected from Group 2, Group 8, Group 9, Group 10, Group 11, Group 12, Group 13, and Group At least one metal selected from Group 14 is more preferable, and it is particularly preferable to include it as a main component.

Examples of the metal include copper, silver, gold, platinum, palladium, nickel, tin, cobalt, rhodium, iridium, iron, ruthenium, osmium, manganese, molybdenum, tungsten, niobium, tantel, titanium, bismuth, antimony, Examples thereof include lead and alloys thereof. Among these, in view of excellent conductivity, those mainly containing silver or those containing an alloy of silver and a metal other than silver are preferable.
Containing mainly the above-mentioned silver means containing 50 mass% or more, preferably 90 mass% or more of silver in the metal nanowire.
Examples of the metal used in the aforementioned alloy with silver include platinum, osmium, palladium and iridium. These may be used alone or in combination of two or more.

There is no restriction | limiting in particular as a shape of the above-mentioned metal nanowire, According to the objective, it can select suitably, For example, it can take arbitrary shapes, such as a column shape, a rectangular parallelepiped shape, and a column shape whose section becomes a polygon. However, in applications where high transparency is required, a cylindrical shape and a cross-sectional shape with rounded polygonal corners are preferred.
The cross-sectional shape of the aforementioned metal nanowire can be examined by applying a metal nanowire aqueous dispersion on a substrate and observing the cross-section with a transmission electron microscope (TEM).
The above-mentioned corner of the cross section of the metal nanowire means a peripheral portion of a point that extends each side of the cross section and intersects with a perpendicular drawn from an adjacent side. Further, “each side of the cross section” is a straight line connecting these adjacent corners. In this case, the ratio of the above-mentioned “periphery length of the cross section” to the total length of the “each side of the cross section” was defined as the sharpness. For example, in the metal nanowire cross section as shown in FIG. 9, the sharpness can be represented by the ratio of the outer peripheral length of the cross section indicated by the solid line and the outer peripheral length of the pentagon indicated by the dotted line. A cross-sectional shape having a sharpness of 75% or less is defined as a cross-sectional shape having rounded corners. The sharpness is preferably 60% or less, and more preferably 50% or less. If the sharpness exceeds 75%, electrons may be localized at this corner and plasmon absorption may increase, or the transparency may deteriorate due to a yellowish color remaining. Moreover, the linearity of the edge part of a pattern may fall and a shakiness may arise. The lower limit of the sharpness is preferably 30%, more preferably 40%.

The average minor axis length (sometimes referred to as “average minor axis diameter” or “average diameter”) of the metal nanowire is preferably 150 nm or less, more preferably 1 nm to 40 nm, and even more preferably 10 nm to 40 nm. 15 nm to 35 nm is particularly preferable.
When the average minor axis length is less than 1 nm, the oxidation resistance may be deteriorated and the durability may be deteriorated. When the average minor axis length is more than 150 nm, scattering due to metal nanowires occurs and sufficient transparency is obtained. There are things you can't get.
The average minor axis length of the above-mentioned metal nanowires was determined by observing 300 metal nanowires using a transmission electron microscope (TEM; manufactured by JEOL Ltd., JEM-2000FX). The average minor axis length of the wire was determined.
The short axis length when the short axis of the metal nanowire is not circular was the shortest axis.

The average major axis length (sometimes referred to as “average length”) of the metal nanowire is preferably 1 μm to 40 μm, more preferably 3 μm to 35 μm, and even more preferably 5 μm to 30 μm.
If the average major axis length is less than 1 μm, it is difficult to form a dense network and sufficient conductivity may not be obtained. If it exceeds 40 μm, the metal nanowires are too long. It may become entangled during production, and aggregates may be produced during the production process.
The average major axis length of the metal nanowires described above was observed from 300 metal nanowires using, for example, a transmission electron microscope (TEM; manufactured by JEOL Ltd., JEM-2000FX). The average major axis length of the nanowire was determined. In addition, when the above-mentioned metal nanowire was bent, the circle | round | yen which makes it an arc was considered and the value calculated from the radius and curvature was made into the major axis length.

The thickness of the conductive photocurable resin layer is preferably from 0.1 to 20 μm, and preferably from 0.5 to 18 μm, from the viewpoint of process suitability such as the stability of the coating liquid and drying during coating and development time during patterning. More preferably, 1-15 micrometers is especially preferable.
The content of the conductive fiber based on the total solid content of the conductive photocurable resin layer is preferably 0.01 to 50% by mass from the viewpoint of conductivity and the stability of the coating liquid, and is preferably 0.05 to 30 mass% is still more preferable, and 0.1-20 mass% is especially preferable.

--Colorant (when used as a mask layer)-
Moreover, when using the above-mentioned photosensitive film as a mask layer, a coloring agent can be used for a photocurable resin layer. As the colorant used in the present invention, known colorants (organic pigments, inorganic pigments, dyes, etc.) can be suitably used. In the present invention, in addition to the black colorant, a mixture of pigments such as red, blue, and green can be used.

  When using the above-mentioned photocurable resin layer as a black mask layer, it is preferable that a black colorant is included from the viewpoint of optical density. Examples of the black colorant include carbon black, titanium carbon, iron oxide, titanium oxide, and graphite. Among these, carbon black is preferable.

  When the above-mentioned photocurable resin layer is used as a white mask layer, white pigments described in paragraphs 0015 and 0114 of JP-A-2005-7765 can be used. In order to use it as a mask layer of other colors, pigments or dyes described in paragraphs 0183 to 0185 of Japanese Patent No. 4546276 may be mixed and used. Specifically, pigments and dyes described in paragraphs 0038 to 0054 of JP-A-2005-17716, pigments described in paragraphs 0068 to 0072 of JP-A-2004-361447, paragraphs of JP-A-2005-17521 The colorants described in 0080 to 0088 can be suitably used.

The aforementioned colorant (preferably a pigment, more preferably carbon black) is desirably used as a dispersion. This dispersion can be prepared by adding and dispersing a composition obtained by previously mixing the aforementioned colorant and pigment dispersant in an organic solvent (or vehicle) described later. The aforementioned vehicle refers to a portion of the medium in which the pigment is dispersed when the paint is in a liquid state. The liquid is a component that binds with the pigment and forms a coating film (binder) and dissolves this. Component to dilute (organic solvent).
The disperser used for dispersing the pigment is not particularly limited. For example, the kneader described in Kazuzo Asakura, “Encyclopedia of Pigments”, First Edition, Asakura Shoten, 2000, Item 438. , Known dispersers such as a roll mill, an atrider, a super mill, a dissolver, a homomixer, a sand mill, and a bead mill.
Further, fine grinding may be performed using frictional force by mechanical grinding described in page 310 of this document.

  From the viewpoint of dispersion stability, the above-mentioned colorant is preferably a colorant having a number average particle diameter of 0.001 μm to 0.1 μm, and more preferably 0.01 μm to 0.08 μm. The “particle size” as used herein refers to the diameter when the electron micrograph image of the particle is a circle of the same area, and the “number average particle size” refers to the above-mentioned particle size for a number of particles. Of these, an average value of 100 particle diameters arbitrarily selected.

The layer thickness of the photocurable resin layer containing the colorant is preferably 0.5 to 10 μm, more preferably 0.8 to 5 μm, and particularly preferably 1 to 3 μm from the viewpoint of a difference in thickness from the other layers. Although there is no restriction | limiting in particular as content rate of the coloring agent in solid content of the above-mentioned colored photosensitive resin composition, It is preferable that it is 15-70 mass% from a viewpoint which shortens image development time enough, 20-20. More preferably, it is 60 mass%, and it is still more preferable that it is 25-50 mass%.
The total solid content as used in this specification means the total mass of the non-volatile component remove | excluding the solvent etc. from the coloring photosensitive resin composition.

  In addition, when forming an insulating layer using the above-mentioned photosensitive film, the layer thickness of a photocurable resin layer is 0.1-5 micrometers from a viewpoint of maintenance of insulation, and 0.3-3 micrometers is still more. 0.5 to 2 μm is particularly preferable.

-Other additives-
Furthermore, other additives may be used for the above-mentioned photocurable resin layer. As the aforementioned additive, the same additives as those used for the transfer film of the present invention can be used.
Moreover, as a solvent at the time of manufacturing the above-mentioned photosensitive film by application | coating, the solvent similar to what is used for the transfer film of this invention can be used.

  As mentioned above, although the case where the above-mentioned photosensitive film was a negative type material was demonstrated centering, the above-mentioned photosensitive film may be a positive type material. In the case where the above-described photosensitive film is a positive type material, for example, a material described in JP-A-2005-221726 is used for the photocurable resin layer, but is not limited thereto.

(Formation of mask layer and insulating layer with photosensitive film)
The mask layer 2 and the insulating layer 5 described above can be formed by transferring the photocurable resin layer to the front plate 1 or the like using the above-described photosensitive film. For example, when the black mask layer 2 is formed, the above-described black film is used on the surface of the front plate 1 using the above-described photosensitive film having the black photo-curable resin layer as the above-described photo-curable resin layer. It can be formed by transferring the photocurable resin layer. When the insulating layer 5 is formed, the above-described photosensitive film having an insulating photo-curable resin layer as the above-described photo-curable resin layer is used to form the first transparent electrode pattern described above. It can be formed by transferring the above-mentioned photocurable resin layer to the surface of the face plate 1.
Further, in the formation of the mask layer 2 that needs light shielding properties, the above photosensitive film having a specific layer structure having a thermoplastic resin layer between the photocurable resin layer and the temporary support is used for photosensitivity. It is possible to prevent the generation of bubbles during film lamination and to form a high quality mask layer 2 or the like having no light leakage.

(Formation of first and second transparent electrode patterns and other conductive elements by a photosensitive film)
The first transparent electrode pattern 3, the second transparent electrode pattern 4, and the other conductive element 6 are etched using the above-described photosensitive film having an etching process or a conductive photo-curable resin layer, or photosensitive. A film can be formed using the lift-off material.

-Etching treatment-
When the first transparent electrode pattern 3, the second transparent electrode pattern 4, and another conductive element 6 are formed by etching, first, on the non-contact surface of the front plate 1 on which the mask layer 2 and the like are formed A transparent electrode layer such as ITO is formed by sputtering. Next, an etching pattern is formed by exposure / development using the above-described photosensitive film having an etching photo-curable resin layer as the above-described photo-curable resin layer on the above-described transparent electrode layer. Thereafter, the transparent electrode layer is etched to pattern the transparent electrode, and the etching pattern is removed, whereby the first transparent electrode pattern 3 and the like can be formed.

  Also when using the above-mentioned photosensitive film as an etching resist (etching pattern), a resist pattern can be obtained in the same manner as described above. For the above-described etching, etching or resist stripping can be applied by a known method described in paragraphs 0048 to 0054 of JP2010-152155A.

  For example, as an etching method, a commonly performed wet etching method in which the substrate is immersed in an etching solution can be used. As an etchant used for wet etching, an acid type or alkaline type etchant may be appropriately selected in accordance with an object to be etched. Examples of acidic etching solutions include aqueous solutions of acidic components such as hydrochloric acid, sulfuric acid, hydrofluoric acid, and phosphoric acid, and mixed aqueous solutions of acidic components and salts of ferric chloride, ammonium fluoride, potassium permanganate, and the like. Is done. As the acidic component, a combination of a plurality of acidic components may be used. In addition, alkaline type etching solutions include sodium hydroxide, potassium hydroxide, ammonia, organic amines, aqueous solutions of alkali components such as organic amine salts such as tetramethylammonium hydroxide, alkaline components and potassium permanganate. A mixed aqueous solution of a salt such as A combination of a plurality of alkali components may be used as the alkali component.

The temperature of the etching solution is not particularly limited, but is preferably 45 ° C. or lower. The resin pattern used as an etching mask (etching pattern) in the present invention is formed by using the above-described photo-curable resin layer, and thus is particularly suitable for acidic and alkaline etching solutions in such a temperature range. Excellent resistance. Therefore, the resin pattern is prevented from peeling off during the etching process, and the portion where the resin pattern does not exist is selectively etched.
After the above-described etching, a cleaning process and a drying process may be performed as necessary to prevent line contamination. For the cleaning process, for example, the base material is cleaned with pure water for 10 to 300 seconds at room temperature, and for the drying process, the air blow pressure (about 0.1 to 5 kg / cm ² ) is appropriately adjusted using an air blow. Just do it.

  Next, the peeling method of the resin pattern is not particularly limited, and examples thereof include a method of immersing the substrate in a peeling solution being stirred at 30 to 80 ° C., preferably 50 to 80 ° C. for 5 to 30 minutes. The resin pattern used as an etching mask in the present invention exhibits excellent chemical resistance at 45 ° C. or lower as described above, but exhibits a property of swelling by an alkaline stripping solution when the chemical temperature is 50 ° C. or higher. . Due to such properties, when the peeling step is performed using a peeling solution of 50 to 80 ° C., there is an advantage that the process time is shortened and the peeling residue of the resin pattern is reduced. That is, by providing a difference in chemical temperature between the above-described etching step and the peeling step, the resin pattern used as an etching mask in the present invention exhibits good chemical resistance in the etching step, while the peeling step. In this case, good releasability is exhibited, and both contradictory properties of chemical resistance and releasability can be satisfied.

  Examples of the stripping solution include inorganic alkali components such as sodium hydroxide and potassium hydroxide, organic alkali components such as tertiary amine and quaternary ammonium salt, water, dimethyl sulfoxide, N-methylpyrrolidone, or these. A stripping solution dissolved in a mixed solution of You may peel by the spray method, the shower method, the paddle method etc. using the above-mentioned stripping solution.

-Photosensitive film having a conductive photocurable resin layer-
In the case where the first transparent electrode pattern 3, the second transparent electrode pattern 4 and the other conductive element 6 are formed using the above-described photosensitive film having the conductive photocurable resin layer, It can be formed by transferring the conductive photocurable resin layer described above to the surface of the face plate 1.
When the first transparent electrode pattern 3 and the like described above are formed using the photosensitive film having the conductive photocurable resin layer, the resist component can be removed from the opening even on the substrate (front plate) having the opening. In addition, it is possible to manufacture a touch panel having a merit of thin layer / light weight by a simple process without contaminating the back side of the substrate.
Furthermore, by using the above-mentioned photosensitive film having a specific layer structure having a thermoplastic resin layer between the conductive photocurable resin layer and the temporary support for forming the first transparent electrode pattern 3 and the like. It is possible to prevent the generation of bubbles when laminating the photosensitive film, and to form the first transparent electrode pattern 3, the second transparent electrode pattern 4, and another conductive element 6 with excellent conductivity and low resistance.

-Use of photosensitive film as lift-off material-
Moreover, a 1st transparent electrode layer, a 2nd transparent electrode layer, and another electroconductive member can also be formed using the above-mentioned photosensitive film as a lift-off material.
In this case, after patterning using the above-described photosensitive film, a transparent conductive layer is formed on the entire surface of the substrate, and then the above-described photocurable resin layer is dissolved and removed together with the deposited transparent conductive layer to obtain a desired transparent A conductive layer pattern can be obtained (lift-off method).

[Image display device]
An image display device according to the present invention includes the capacitive input device according to the present invention.
The capacitive input device of the present invention and an image display device including the capacitive input device as constituent elements are “latest touch panel technology” (Techno Times, issued July 6, 2009), Mitani. Yuji's supervision, “Touch Panel Technology and Development”, CM Publishing (2004, 12), FPD International 2009 Forum T-11 Lecture Textbook, Cypress Semiconductor Corporation Application Note AN2292, etc. can be applied. .

  The present invention will be described more specifically with reference to the following examples. The materials, amounts used, ratios, processing details, processing procedures, and the like shown in the following examples can be changed as appropriate without departing from the spirit of the present invention. Therefore, the scope of the present invention is not limited to the specific examples shown below. Unless otherwise specified, “part” and “%” are based on mass.

[Example 1]
[Production of Transfer Film I1 with First and Second Curable Transparent Resin Layers]
<Formation of first curable transparent resin>
Using a slit-shaped nozzle on a 75 μm thick polyethylene terephthalate film (temporary support), the first coating liquid for curable transparent resin layer having the following formulation OC1 has a desired film thickness described in the following table. After being adjusted and coated, dried at 100 ° C. for 2 minutes, further dried at 120 ° C. for 1 minute and dried to form a first curable transparent resin layer.

(First coating liquid for curable transparent resin layer: formulation OC1)
Polymerizable compound (pentaerythritol tetraacrylate, NK ester A-TMMT, Shin-Nakamura Chemical Co., Ltd.%): 84.8 parts by mass Polymer solution 1 (see paragraph No. [0061] of JP-A-2008-146018) Structural formula P-25: Glycidyl methacrylate adduct (d) (composition (mol%): a / b / c / d of cyclohexyl methacrylate (a) / methyl methacrylate (b) / methacrylic acid copolymer (c) = 46/2/20/32, weight average molecular weight: 36000, acid value 66 mgKOH / g) 1-methoxy-2-propanol, methyl ethyl ketone solution (solid content: 45%)): 251 parts by mass / photopolymerization initiator ( 1,2-octanedione, 1- [4- (phenylthio)-, 2- (O-benzoyloxime)], trade name: IRG CURE OXE-01, manufactured by BASF)
: 2.09 parts by mass-Surfactant (trade name: Megafac F-784F, manufactured by Dainippon Ink): 0.11 parts by mass-methyl ethyl ketone: 379 parts by mass-MMPGAc (propylene glycol monomethyl ether acetate, Daicel Chemical Co., Ltd. ) Product: 283 parts by mass The details of the formulation OC1 are shown in Table 1 below together with the details of the formulations OC2, OC3, OC4, T1, and IM40.

<Formation of second curable transparent resin layer>
Next, on the first curable transparent resin layer, a second curable transparent resin layer coating liquid composed of the following formulation IM1 is adjusted and applied so as to have a desired film thickness described in the following table. The film was dried at 80 ° C. for 1 minute and further dried at 110 ° C. for 1 minute to form a second curable transparent resin layer.

・バインダー水溶液（アセタール化度 ９ｍｏｌ％、水酸基含有量 ９０ｍｏｌ％のポリビニルアセタール樹脂２０％水溶液、商品名：エスレックＫＷ−１、積水化学工業（株）製） ：２０．７質量部
・水溶性光重合性開始剤（ＩＲＧＡＣＵＲＥ ２９５９、ＢＡＳＦジャパン（株））
：０．３０５質量部
処方ＩＭ１の詳細を、処方ＩＭ１〜１４、ＩＭ２７〜２９およびＩＭ４１の詳細とあわせて下記表２に示し、処方ＩＭ１５〜２６およびＩＭ３０〜３２の詳細を下記表３に示した。 (Second curable transparent resin layer coating solution: Formulation IM1)
Methanol: 333 parts by mass Zirconia (ZrO ₂ ) dispersion (trade name: Nanouse OZ-S30M; manufactured by Nissan Chemical Industries, Ltd., inorganic particles 30.5%, organic acid 2.8%, methanol: 66.7 %)
: 48.3 parts by mass-ion-exchanged water: 595 parts by mass-Water-soluble polymerizable compound of the following structural formula 1: 3.10 parts by mass

-Binder aqueous solution (Acetalization degree 9 mol%, hydroxyl group content 90 mol% polyvinyl acetal resin 20% aqueous solution, trade name: ESREC KW-1, manufactured by Sekisui Chemical Co., Ltd.): 20.7 parts by mass Water-soluble photopolymerization Sex initiator (IRGACURE 2959, BASF Japan Ltd.)
: 0.305 parts by mass Details of the formulation IM1 are shown in Table 2 below together with details of the formulations IM1-14, IM27-29 and IM41, and details of the formulations IM15-26 and IM30-32 are shown in Table 3 below .

ZrO ₂ used for the zirconia dispersion in IM1 is a particle having a refractive index of 2.2 and an average particle diameter of about 12 nm. Further, the content (mass ratio) of the inorganic particles with respect to all solid contents contained in the coating solution was determined and listed in the following table. In the table below, “wt%” is synonymous with “mass%”.
For all water and alcohol having 1 to 3 carbon atoms contained in the coating solution containing methanol in the zirconia dispersion and water in the binder aqueous solution, the water content / mass ratio of 1 to 3 carbon atoms is expressed as follows. It was calculated and listed in the table below.

<Evaluation of first or second curable transparent resin layer>
(Evaluation of refractive index of first or second curable transparent resin layer)
The average refractive index in the light which has a wavelength of 400-750 nm of the 1st or 2nd curable transparent resin layer was calculated | required, and it described in the following table | surface.

(Evaluation of water solubility of the first or second curable transparent resin layer)
Using a slit-shaped nozzle on a 75 μm thick polyethylene terephthalate film (temporary support), the first or second curable transparent resin layer coating solution is adjusted to a desired thickness and applied. did. When the first or second curable transparent resin layer coating solution was repelled by the temporary support and could not be applied, the temporary support was subjected to a hydrophilic treatment by corona treatment in advance.
After the coating film of the first or second curable transparent resin layer coating liquid is dried at 100 ° C. for 2 minutes, the coating film is further dried at 120 ° C. for 1 minute to obtain the first and second curable transparent resin layers. Formed.
The first or second curable transparent resin layer was conditioned at 23 ° C. and a relative humidity of 55% for 1 hour and immersed in ion-exchanged water at 25 ° C. The immersion time is 3 minutes / μm per unit film thickness, that is, the film thickness of the first or second curable transparent resin layer (μm) ÷ 1 (μm) × 3 minutes (for example, 15 minutes in the case of 5 μm) In the case of 80 nm = 0.08 μm, 0.24 minutes = 14.4 seconds).
Then, the surface of the 1st or 2nd curable transparent resin layer was lightly rinsed using the ion exchange water contained in the washing bottle.
"Evaluation criteria"
Water-solubility: The first or second curable transparent resin layer was completely dissolved and removed from the entire surface of the temporary support with an immersion time of 3 minutes / μm per unit film thickness.
Water-insoluble: The first or second curable transparent resin layer could not be completely removed from the entire surface of the temporary support at an immersion time of 3 minutes / μm per unit film thickness, and thus could not be completely removed. A residue of the first or second curable transparent resin layer remains.
The evaluation results are listed in the table below.

(Evaluation of binder SP value difference)
Differences in the SP values of the binders used for the first or second curable transparent resin layer were determined and listed in the table below.

<Press bonding of protective film>
Thus, after providing the 1st curable transparent resin layer and 2nd curable transparent resin layer which become the dry film thickness in the following table | surface on a temporary support body, it is finally a protective film (thickness). 12 μm polypropylene film).

  Thus, a transfer film in which the temporary support, the first curable transparent resin layer, the second curable transparent resin layer, and the protective film were integrated was produced. The obtained transfer film was designated as transfer film I1 of Example 1.

<Evaluation of transfer film>
(Evaluation of layer fractionation)
In the production of the transfer film provided with the first and second curable transparent resin layers, the second curable transparent resin layer coating solution is applied on the first curable transparent resin layer and dried. The layers were observed for mixing. Furthermore, the cross section of the dried transfer film was observed with the electron microscope, and it was evaluated whether the layer was fractionated. A or B is at a practical level and is preferably A.
"Evaluation criteria"
A: In the coating and drying process of the second curable transparent resin layer coating solution, the first curable transparent resin layer was not dissolved or clouded. Moreover, as a result of observing the cross section of the transfer film with an electron microscope, the layer was properly fractionated and the layer fraction was good.
B: In the coating and drying process of the second coating liquid for the curable transparent resin layer, the first curable transparent resin layer was slightly clouded but disappeared after drying. Moreover, as a result of observing the cross section of the transfer film with an electron microscope, the layer is fractionated, and the layer fraction is normal.
C: In the coating and drying process of the second curable transparent resin layer coating solution, the first curable transparent resin layer was dissolved or slightly clouded. Moreover, as a result of observing a cross section of the transfer film with an electron microscope, the first curable transparent resin layer and the second curable transparent resin layer are slightly mixed or wavy, and the layer fraction is poor.
D: In the coating and drying process of the second curable transparent resin layer coating solution, the first curable transparent resin layer was dissolved or clouded. Moreover, as a result of observing the cross section of the transfer film with an electron microscope, the layers are completely mixed and the layer fraction is very poor.
The results obtained are listed in the table below.

<Evaluation of cracks>
On the temporary support, the transfer film prepared by laminating the first curable transparent resin layer and the second curable transparent resin layer in this order is wound around a rod having a different diameter and bent, This was done by observing with an optical microscope. A, B or C is preferred, A or B is more preferred, and A is particularly preferred.
"Evaluation criteria"
A: Even if it is wound around a 2 mmφ rod and bent, it does not crack.
B: There is no crack even if it is wound around a 3 mmΦ rod and bent.
C: Even if it is wound around a 4 mmφ rod and bent, it does not crack.
D: No cracking even when wound around a 5 mmΦ rod and bent.
E: Slightly cracked cracks are present when the transfer film is produced.
The results obtained are listed in the table below.

(Reticulation evaluation)
The transfer film prepared by laminating the first curable transparent resin layer and the second curable transparent resin layer in this order on the temporary support was left for 24 hours in an environment of 23 ° C. and 50% relative humidity. Then, it observed with the microscope from the 2nd curable transparent resin layer surface side using reflected light and transmitted light, and evaluated according to the following reference | standard. A, B or C is preferred, A or B is more preferred, and A is particularly preferred.
"Evaluation criteria"
A: The occurrence of fine “wrinkles” on the surface is not recognized at all, and is very good.
B: Extremely weak “wrinkles” were observed only in the edge portions of the film, but the occurrence of wrinkles in the other portions was not observed at all.
C: The occurrence of fine wrinkles on the surface was slightly observed, but it was not recognized visually and was normal at a level where there was no practical problem.
D: The occurrence of fine “wrinkles” is considerably recognized and is a bad level.
E: The occurrence of fine “wrinkles” is recognized on the entire surface, which is a very bad level.
The evaluation results are listed in the table below.

(Production of transparent laminate)
Using the transfer film I1 of Example 1 obtained above, a transparent laminate was produced by the following method.

<1. Formation of transparent film>
A transparent film having a refractive index of 1.60 and a film thickness of 80 nm using T1 shown in Table 1 was formed on a glass transparent substrate (glass substrate) having a refractive index of 1.51 by the following method.

(Production of transfer material)
On a 75 μm-thick polyethylene terephthalate film (temporary support), a slit-shaped nozzle was used to apply a coating solution for a thermoplastic resin layer having the following formulation H1, followed by drying to form a thermoplastic resin layer. Next, an intermediate layer coating solution having the following formulation P1 was applied onto the thermoplastic resin layer and dried to form an intermediate layer.
Furthermore, the coating liquid T1 for transparent curable compositions was apply | coated and dried, and the transparent resin layer was formed. Thus, a thermoplastic resin layer having a dry film thickness of 15.1 μm, an intermediate layer having a dry film thickness of 1.6 μm, and a transparent resin layer having a dry film thickness of 80 nm were provided on the temporary support. Finally, a protective film (thickness 12 μm polypropylene film) was pressure-bonded on the transparent resin layer. Thus, a transfer material in which the temporary support, the thermoplastic resin layer, the intermediate layer (oxygen barrier film), the transparent resin layer, and the protective film were integrated was produced.

(Coating solution for thermoplastic resin layer: Formulation H1)
Methanol: 11.1 parts by mass Propylene glycol monomethyl ether acetate: 6.36 parts by mass Methyl ethyl ketone: 52.4 parts by mass Methyl methacrylate / 2-ethylhexyl acrylate / benzyl methacrylate / methacrylic acid copolymer (copolymerization composition ratio) (Molar ratio) = 55 / 11.7 / 4.5 / 28.8, weight average molecular weight = 100,000, Tg (glass transition temperature) ≈70 ° C.): 5.83 parts by mass / styrene / acrylic acid copolymer (Copolymerization composition ratio (molar ratio) = 63/37, weight average molecular weight = 10,000, Tg≈100 ° C.): 13.6 parts by mass / monomer 1 (trade name: BPE-500, Shin-Nakamura Chemical Co., Ltd.) Ltd.): 9.1 parts by mass fluorine-based polymer: 0.54 parts by mass the above fluorine-containing _{polymer, C 6 F 13 CH 2 CH} 2 OCOCH = CH 2 4 Parts and _{H (OCH (CH 3) CH} 2) 7 with a copolymer of OCOCH = CH ₂ 55 parts of _{H (OCHCH 2) 7 OCOCH =} CH 2 5 parts, weight average molecular weight 30,000, methyl ethyl ketone 30 wt% solution (Product name: MegaFuck F780F, manufactured by Dainippon Ink & Chemicals, Inc.).

(Coating liquid for intermediate layer: prescription P1)
Polyvinyl alcohol: 32.2 parts by mass (trade name: PVA205, manufactured by Kuraray Co., Ltd., saponification degree = 88%, polymerization degree 550)
・ Polyvinylpyrrolidone: 14.9 parts by mass (trade name: K-30, manufactured by ISP Japan Co., Ltd.)
-Distilled water: 524 parts by mass-Methanol: 429 parts by mass

(Formation of transparent film)
Using the transfer material from which the protective film was peeled off, the transparent resin layer was transferred onto the glass transparent substrate together with the thermoplastic resin, the intermediate layer and the PET temporary support, and then the PET temporary support was peeled off. Next, using a proximity type exposure machine (manufactured by Hitachi High-Tech Electronics Engineering Co., Ltd.) having an ultrahigh pressure mercury lamp, the entire surface was exposed from the thermoplastic resin layer side at i line and 40 mJ / cm ² . Next, a triethanolamine developer (containing 30% triethanolamine, trade name: T-PD2 (manufactured by FUJIFILM Corporation) 10 times with pure water (1 part of T-PD2 and 9 parts of pure water). The mixture was diluted to 30) at 30 C for 60 seconds at a flat nozzle pressure of 0.04 MPa to remove the thermoplastic resin and the intermediate layer. Subsequently, air was sprayed on the upper surface (transparent resin layer side) of the glass transparent substrate to drain the liquid, and then pure was sprayed for 10 seconds by showering, pure shower cleaning was performed, and air was sprayed to spray the liquid on the glass transparent substrate. Reduced stagnation. Next, the glass transparent substrate is heat-treated at 230 ° C. for 60 minutes (post-bake), and the transparent resin layer is heated and cured to obtain a transparent film, whereby a substrate in which the transparent film is laminated on the glass transparent substrate is obtained. It was.

<2. Formation of transparent electrode pattern>
The substrate obtained by laminating a transparent film on the glass transparent substrate obtained above was introduced into a vacuum chamber, and an ITO target having a SnO ₂ content of 10 mass% (indium: tin = 95: 5 (molar ratio) )) To form an ITO thin film having a thickness of 40 nm and a refractive index of 1.82 by DC magnetron sputtering (conditions: substrate temperature 250 ° C., argon pressure 0.13 Pa, oxygen pressure 0.01 Pa) and transparent. A front plate on which an electrode layer was formed was obtained. The surface resistance of the ITO thin film was 80Ω / □.

(Preparation of photosensitive film E1 for etching)
On the polyethylene terephthalate film (temporary support) having a thickness of 75 μm, a coating solution for the thermoplastic resin layer composed of the above-mentioned formulation H1 was applied using a slit nozzle and dried to form a thermoplastic resin layer. . Next, on the thermoplastic resin layer, the intermediate layer coating solution composed of the above-described formulation P1 was applied and dried to form an intermediate layer.
Furthermore, the photocurable resin layer coating solution for etching: Formula E1 was applied and dried to form a photocurable resin layer for etching. Thus, the thermoplastic resin layer having a dry film thickness of 15.1 μm, the intermediate layer having a dry film thickness of 1.6 μm, and the photocurable resin layer for etching having a film thickness of 2.0 μm are formed on the temporary support. A laminate was obtained. Finally, a protective film (thickness 12 μm polypropylene film) was pressure-bonded onto the etching photocurable resin layer. Thus, a transfer material in which the temporary support, the thermoplastic resin layer, the intermediate layer (oxygen barrier film), and the photocurable resin layer for etching were integrated was produced.

(Coating liquid for photocurable resin layer for etching: prescription E1)
Methyl methacrylate / styrene / methacrylic acid copolymer (copolymer composition (mass%): 31/40/29, weight average molecular weight 60000, acid value 163 mg KOH / g)
: 16 parts by mass-Monomer 1 (Brand name: BPE-500, manufactured by Shin-Nakamura Chemical Co., Ltd.): 5.6 parts by mass-Tetraethylene oxide monomethacrylate 0.5 mol adduct of hexamethylene diisocyanate: 7 parts by mass Cyclohexanedimethanol monoacrylate as a compound having one polymerizable group in the molecule 2.8 parts by mass, 2-chloro-N-butylacridone: 0.42 parts by mass, 2,2-bis (o-chlorophenyl) -4,4 ', 5,5'-tetraphenylbiimidazole: 2.17 parts by mass Malachite green oxalate: 0.02 parts by mass Leucocrystal violet: 0.26 parts by mass Phenothiazine: 0.013 parts by mass Part / surfactant (trade name: MegaFuck F-780F, manufactured by Dainippon Ink Co., Ltd.)
: 0.03 parts by mass · Methyl ethyl ketone: 40 parts by mass · 1-methoxy-2-propanol: 20 parts by mass In addition, the coating liquid for photocurable resin layer for etching: The viscosity at 100 ° C after removing the solvent of Formulation E1 is 2500 Pa・ It was sec.

(Formation of transparent electrode pattern)
The front plate on which the transparent electrode layer was formed was washed and laminated with an etching photosensitive film E1 from which the protective film was removed (base material temperature: 130 ° C., rubber roller temperature 120 ° C., linear pressure 100 N / cm, conveyance speed 2. 2 m / min). After peeling off the temporary support, the distance between the exposure mask (quartz exposure mask having a transparent electrode pattern) surface and the photocurable resin layer for etching is set to 200 μm, and the exposure dose is 50 mJ / cm ² (i line). Pattern exposure.
Next, using a triethanolamine developer (containing 30% by mass of triethanolamine, trade name: T-PD2 (manufactured by Fuji Film Co., Ltd.) diluted 10 times with pure water) at 25 ° C., 100 The film was developed for 2 seconds and washed at 33 ° C. for 20 seconds using a surfactant-containing cleaning solution (trade name: T-SD3 (manufactured by FUJIFILM Corporation) diluted 10-fold with pure water). The front plate after the cleaning treatment was rubbed with a rotating brush, and the residue was removed by spraying ultrapure water from an ultrahigh pressure cleaning nozzle. Subsequently, the post-baking process for 130 degreeC for 30 minutes was performed, and the front board in which the transparent electrode layer and the photocurable resin layer pattern for an etching were formed was obtained.
The front plate on which the transparent electrode layer and the photocurable resin layer pattern for etching are formed is immersed in an etching bath containing ITO etchant (hydrochloric acid, potassium chloride aqueous solution, liquid temperature 30 ° C.) and treated for 100 seconds (etching treatment). Then, the transparent electrode layer in the exposed region that was not covered with the photocurable resin layer for etching was dissolved and removed to obtain a front plate with a transparent electrode layer pattern with the photocurable resin layer pattern for etching.
Next, a front plate with a transparent electrode layer pattern with a photocurable resin layer pattern for etching was applied to a resist stripping solution (N-methyl-2-pyrrolidone, monoethanolamine, surfactant (trade name: Surfynol 465). , Manufactured by Air Products Co., Ltd.), immersed in a resist stripping tank containing a liquid temperature of 45 ° C., treated for 200 seconds (peeling treatment), the photocurable resin layer for etching was removed, and a transparent film and a transparent film were formed on the glass transparent substrate. A substrate on which a transparent electrode pattern was formed was obtained.

After imparting conductivity and surface protection to the end of the transparent electrode pattern with Pt coating (about 20 nm thick), using a FEI Nova200 type FIB / SEM compound machine, shape observation of the transparent electrode pattern end (two Next electron image, acceleration voltage 20 kV).
The formed ITO pattern had a tapered shape as shown in FIG. 10, and the taper angle α = about 3 °.

<3. Formation of first curable transparent resin layer and second curable transparent resin layer>
The transfer film I1 of Example 1 from which the protective film had been removed was laminated on the glass transparent substrate obtained above on which the transparent film and the transparent electrode pattern were formed (rubber roller temperature 110 ° C., linear pressure 100 N). / Cm, conveyance speed 2.0 m / min). The distance between the exposure mask (quartz exposure mask having an overcoat formation pattern) surface and the temporary support is set to 125 μm, and pattern exposure is performed through the temporary support at an exposure amount of 100 mJ / cm ² (i-line). did. After the temporary support was peeled off, it was washed for 60 seconds at 32 ° C. with a 2% aqueous solution of sodium carbonate. The front plate after the cleaning treatment was rubbed with a rotating brush, and the residue was removed by spraying ultrapure water from an ultrahigh pressure cleaning nozzle. Subsequently, air was blown to remove moisture on the base material, and a post-bake treatment at 145 ° C. for 30 minutes was performed. A transparent film, a transparent electrode pattern, a second curable transparent resin layer, A transparent laminate in which one curable transparent resin layer was continued in this order was formed.
Thus, the transparent laminated body which laminated | stacked the transparent film | membrane, the transparent electrode pattern, the 2nd curable transparent resin layer, and the 1st curable transparent resin layer in this order on the glass-made transparent substrate was obtained. The obtained transparent laminate was designated as the transparent laminate of Example 1.

[Evaluation of transparent laminate]
<Evaluation of visibility of transparent electrode pattern>
A transparent laminate obtained by laminating a transparent film, a transparent electrode pattern, a second curable transparent resin layer, and a first curable transparent resin layer in this order on a glass transparent substrate, a transparent adhesive tape (manufactured by 3M, The product was bonded to a black PET material via a product name, OCA tape 8171CL), and the entire substrate was shielded from light.
The visibility of the transparent electrode pattern was performed by making light incident on the fluorescent lamp (light source) and the prepared substrate from the glass surface side and visually observing reflected light from the glass surface obliquely in a dark room. A, B or C is at a practical level, preferably A or B, and more preferably A.
"Evaluation criteria"
A: The transparent electrode pattern is not visible at all.
B: The transparent electrode pattern is slightly visible but hardly visible.
C: A transparent electrode pattern is visible (unclear).
D: Although a transparent electrode pattern is visible, it is practically acceptable.
E: The transparent electrode pattern is clearly visible (easy to understand).
The results obtained are listed in the table below.

<Evaluation of coloring>
The transparent laminated body which laminated | stacked the transparent film, the transparent electrode pattern, the 2nd curable transparent resin layer, and the 1st curable transparent resin layer in this order on the glass-made transparent substrate was performed by observing visually. 60 people were observed from the front and back, and the whiteness was evaluated according to the following evaluation criteria. A, B or C is preferred, A or B is more preferred, and A is particularly preferred.
"Evaluation criteria"
A: Number of people recognized as yellowish 0-1 people B: Number of people recognized as yellowish 2-3 People C: Number of people recognized yellowish 4-5 people D: Number of people recognized as yellowish 6-10 people E: Number of people recognized as yellowish 11 or more The results obtained are listed in the table below.

<Evaluation of patterning properties>
A front plate on which a mask layer, a transparent film, a first transparent electrode pattern, an insulating layer pattern, and a second transparent electrode pattern are formed on a glass transparent substrate is used as a second curable transparent resin layer and a first curable transparent film. The resin layers were laminated in this order, and the exposed and developed transparent laminate was observed with an optical microscope. A, B or C is at a practical level, preferably A or B, and more preferably A. .
"Evaluation criteria"
A: The patterning property is very good with no residue in the non-exposed portion of the substrate and the unexposed portion of the display portion, and the absence of a missing portion at the boundary portion between the exposed portion and the unexposed portion.
B: A slight residue is observed in the non-display portion of the substrate, but there is no residue in the unexposed portion of the display portion, and there is no portion lacking in the boundary portion between the exposed portion and the unexposed portion. .
C: A slight residue is observed in the non-display portion of the substrate and the unexposed portion of the display portion. Alternatively, there is a slight chipped portion at the boundary between the exposed portion and the unexposed portion, but the display is not adversely affected and patterning is normal.
D: Residues are observed in the non-display portion of the substrate and the unexposed portion of the display portion. Alternatively, there is a lacking portion at the boundary between the exposed portion and the unexposed portion, which has an adverse effect on the display and the patterning property is poor.
E: The non-display part of the substrate and the unexposed part of the display part are not developed, and many residues are observed. Alternatively, many of the exposed portions are missing, and the display is adversely affected, and the patterning property is very poor.
F: The temporary support could not be peeled from the substrate, and the patterning property could not be evaluated.
The evaluation results are listed in the table below.

(Evaluation of substrate adhesion)
JIS K 5600-5-6: mask layer, transparent film, first transparent electrode pattern, insulating layer pattern, second transparent electrode pattern, second curable transparent resin on glass according to ISO 2409 (cross-cut method) The transparent laminate obtained by laminating the layer and the first curable transparent resin layer in this order was cut with a 1 mm width and peeled off with a cellophane tape to observe whether there was any peeling. A, B or C is preferred, A or B is more preferred, and A is particularly preferred.
<Evaluation criteria>
A: The first and second curable transparent resin layer components were not peeled off at all, and the adhesion was very good.
B: Slight peeling was observed only at the cut edges of the first and second curable transparent resin layers, but the squares were not peeled at all and were at a good level.
C: The peel-off of the first and second curable transparent resin layer components is 0% or more and less than 2%, which is a practical level, and is normal.
D: The peeling of the first and second curable transparent resin layer layer components is bad because peeling of the mass decorating layer component is recognized by 2% or more and less than 5%.
E: Exfoliation of 5% or more of the first and second curable transparent resin layer layer components was observed, which is very bad.
The evaluation results are listed in the table below.

[Examples 2 to 6 and 8]
Instead of using IM1 having a methanol content of 37.5% by mass (alcohol content of 1 to 3 carbon atoms) in the solvent in Example 1, the methanol content in the solvent was 40% by mass (Example 2, IM2), 25 mass% (Example 3, IM3), 12.5 mass% (Example 4, IM4), 6.5 mass% (Example 5, IM5), 3.4 mass% (Example 6, The transfer films and transparent laminates of Examples 2 to 6 and 8 were prepared and evaluated in the same manner as in Example 1 except that they were changed to IM6) and 42% by mass (Example 8, IM8). The evaluation results are listed in the table below.

[Example 7]
In Example 1, a water-dispersed zirconia dispersion was used in place of the methanol-dispersed zirconia dispersion used in IM1 as the second curable transparent resin layer coating solution, and the methanol content in the solvent was 37.5. A transfer film and a transparent laminate of Example 7 were prepared and evaluated in the same manner as in Example 1 except that IM7 changed from 0% by mass to 0% by mass was used. The evaluation results are listed in the table below.

・残存アセチル基量１９．５ｍｏｌ％、鹸化度８１．５ｍｏｌ％、水酸基含有量８１．５ｍｏｌ％、重合度５５０のポリビニルアルコール樹脂（ＰＶＡ４０５、クラレ製）の１０％水溶液（実施例３３、ＩＭ２７）、
・残存アセチル基量２９ｍｏｌ％、鹸化度７１ｍｏｌ％、水酸基含有量７１ｍｏｌ％のポリビニルアルコール樹脂（Ｌ８、クラレ製）の１０％水溶液（実施例３４、ＩＭ２８）、
・残存アセチル基量３４ｍｏｌ％、鹸化度６６ｍｏｌ％、水酸基含有量６６ｍｏｌ％のポリビニルアルコール樹脂の１０％水溶液（実施例３５、ＩＭ２９）
に変更した第二の硬化性透明樹脂層用塗布液を用いた以外は実施例１と同様にして実施例９〜１４および３３〜３５の転写フィルムおよび透明積層体を作製して、評価を行った。評価した結果を下記表に記載した。 [Examples 9-14 and 33-35]
In Example 1, a 20% aqueous solution of polyvinyl acetal resin having a degree of acetalization of 9 mol% and a hydroxyl group content of 90 mol% (trade name, manufactured by Sekisui Chemical Co., Ltd.) used in IM1 as the second curable transparent resin layer coating solution. : In place of ESREC KW-1): 20% aqueous solution of polyvinyl acetal resin having a degree of acetalization of 30 mol% and a hydroxyl group content of 70 mol% (trade name: ESREC KW-3, manufactured by Sekisui Chemical Co., Ltd.) (Examples) 9, IM9),
Acetalization degree 8 mol%, hydroxyl content 91 mol% polyvinyl acetal resin 25% aqueous solution (trade name: ESREC KW-10, manufactured by Sekisui Chemical Co., Ltd.) (Example 10, IM10),
-10% aqueous solution (Example 11, IM11) of polyvinyl alcohol resin (PVA205C, manufactured by Kuraray Co., Ltd.) having a residual acetyl group amount of 12 mol%, a saponification degree of 88 mol%, a hydroxyl group content of 88 mol%, and a polymerization degree of 550,
-10% aqueous solution (Example 12, IM12) of polyvinyl alcohol resin (PVA217C, manufactured by Kuraray) having a residual acetyl group amount of 12 mol%, a saponification degree of 88 mol%, a hydroxyl group content of 88 mol%, and a polymerization degree of 1750,
-10% aqueous solution (Example 13, IM13) of polyvinyl alcohol resin (PVA124C, manufactured by Kuraray Co., Ltd.) having a residual acetyl group amount of 1.5 mol%, a saponification degree of 98.5 mol%, a hydroxyl group content of 98.5 mol%, and a polymerization degree of 2400,
A 10% aqueous solution of a modified polyvinyl alcohol resin (compound P below) having a saponification degree of 96.3 mol%, a hydroxyl group content of 96.3 mol%, and a polymerization degree of 550 (Example 14, IM14),

-10% aqueous solution (Example 33, IM27) of polyvinyl alcohol resin (PVA405, manufactured by Kuraray Co., Ltd.) having a residual acetyl group amount of 19.5 mol%, a saponification degree of 81.5 mol%, a hydroxyl group content of 81.5 mol%, and a polymerization degree of 550,
A 10% aqueous solution (Example 34, IM28) of a polyvinyl alcohol resin (L8, manufactured by Kuraray) having a residual acetyl group content of 29 mol%, a saponification degree of 71 mol%, and a hydroxyl group content of 71 mol%,
A 10% aqueous solution of polyvinyl alcohol resin having a residual acetyl group amount of 34 mol%, a saponification degree of 66 mol%, and a hydroxyl group content of 66 mol% (Example 35, IM29)
The transfer films and transparent laminates of Examples 9-14 and 33-35 were prepared and evaluated in the same manner as in Example 1 except that the second coating liquid for curable transparent resin layer was used. It was. The evaluation results are listed in the table below.

[Examples 15 to 17]
In Example 1, as the second coating liquid for the curable transparent resin layer, the polymerizable compound of the structural formula 1 used for IM1, respectively,
NK ester A-TMM3LM-N (Shin Nakamura Chemical Co., Ltd., made of a mixture of pentaerythritol tetraacrylate and triacrylate, 57% triacrylate) (Example 15),
NK ester A-TMM-3L (manufactured by Shin-Nakamura Chemical Co., Ltd., mixture of pentaerythritol tetraacrylate and triacrylate, 55% triacrylate) (Example 16),
NK ester A-TMM3 (manufactured by Shin-Nakamura Chemical Co., Ltd., mixture of pentaerythritol tetraacrylate and triacrylate, 37% triacrylate) (Example 17)
The transfer films and transparent laminates of Examples 15 to 17 were prepared and evaluated in the same manner as in Example 1 except that IM15 to 17 changed to were used. The evaluation results are listed in the table below.

[Example 18]
In Example 1, as the second curable transparent resin layer coating solution, except that IM18 in which IRGCURE2959 used in IM1 was changed to a photopolymerization initiator of the following structural formula 2 was used, the same as in Example 1. The transfer film and transparent laminate of Example 18 were produced and evaluated. The evaluation results are listed in the table below.

[Examples 19 to 24]
In Example 1, 80% by mass (Example 19, IM19), 73% by mass (Example 20, IM20), and 60.6% by mass of IM1 having a zirconia fine particle content of 66% by mass in the solid content ( Example 21, IM21), 57.1% by weight (Example 22, IM22), 50% by weight (Example 23, IM23), second curing changed to 40.1% by weight (Example 24, IM24) The transfer films and transparent laminates of Examples 19 to 24 were prepared and evaluated in the same manner as in Example 1 except that the coating solution for the transparent resin layer was used. The evaluation results are listed in the table below.

[Examples 25, 31 and 32]
In Example 1, the formulation of the first coating liquid for the curable transparent resin layer was changed from OC1 having a refractive index of 1.51 to OC2 (Example 25) and OC3 (Example of Table 1) having a refractive index of 1.53. 31) Except for changing to OC4 (Example 32), the transfer films and transparent laminates of Examples 25, 31 and 32 were prepared and evaluated in the same manner as in Example 1. The evaluation results are listed in the table below.

[Example 26]
In Example 1, the transfer film and the transparent laminate of Example 26 were produced and evaluated in the same manner as in Example 1 except that the thickness of the first curable transparent resin layer was changed from 5 μm to 8 μm. . The evaluation results are listed in the table below.

[Example 27]
In Example 22, the transfer film and transparent laminate of Example 27 were produced and evaluated in the same manner as in Example 22 except that the thickness of the second curable transparent resin layer was changed from 70 nm to 100 nm. . The evaluation results are listed in the table below.

[Example 28]
In Example 1, the thickness of the second curable transparent resin layer was changed from 70 nm to 35 nm, and IM40 was second cured as a third curable transparent resin layer on the second curable transparent resin layer. The transfer film of Example 28 was produced and evaluated in the same manner as in Example 1 except that the thickness was 35 nm as in the case of the transparent transparent resin layer.
In Example 1, a transparent film, a transparent electrode pattern, and a third cure were formed on a glass transparent substrate in the same manner as in Example 1 except that the transfer film of Example 28 was used instead of the transfer film of Example 1. The transparent laminated body of Example 28 with which the transparent transparent resin layer, the 2nd curable transparent resin layer, and the 1st curable transparent resin layer were continued in this order was produced, and evaluation was performed. The evaluation results are listed in the table below.

[Examples 29 and 30]
In Example 1, instead of IM1 containing no polymer particles as the second curable transparent resin layer coating solution, an aqueous dispersion of polyethylene ionomer (trade name: Chemipearl S120, manufactured by Mitsui Chemicals) and a polyether polyurethane Transfer of Examples 29 and 30 in the same manner as in Example 1 except that IM25 and IM26 containing 21.2% by mass of an aqueous dispersion (trade name: Hydran WLS201 DIC Co., Ltd.) were used. A film and a transparent laminate were produced and evaluated. The evaluation results are listed in the table below.

[Comparative Examples 1 and 2]
In Example 1, as a coating liquid for the second curable transparent resin layer, instead of IM1, IM40 (Comparative Example 1) having the formulation described in Table 1 and IM30 (Comparative Example 2) described in Table 3 were used. The transfer films and transparent laminates of Comparative Examples 1 and 2 were prepared and evaluated in the same manner as in Example 1 except that was used.
IM40 and IM30 melt | dissolved the 1st curable transparent resin layer, the 1st curable transparent resin layer and the 2nd curable transparent resin layer mixed, and the transparent electrode pattern visibility deteriorated remarkably. The evaluation results are shown in the following table together with other evaluation results. In Comparative Example 2, the evaluation of cracking and reticulation of the transfer film and the evaluation of substrate adhesion of the transparent laminate were not performed.

[Comparative Example 3]
In Example 1, as a second curable transparent resin layer coating solution, a comparative material was prepared in the same manner as in Example 1 except that a transfer material was prepared using IM31 having the formulation shown in Table 3 above instead of IM1. The transfer film 3 and the transparent laminate were prepared and evaluated.
IM31 did not dissolve and cloud the first curable transparent resin layer, and the first curable transparent resin layer and the second curable transparent resin layer could be fractionated. However, since the refractive index of the first curable transparent resin layer was 1.59, the visibility of the transparent electrode pattern was significantly reduced. The evaluation results are shown in the following table together with other evaluation results.

[Comparative Example 4]
In Example 1, Comparative Example 4 was carried out in the same manner as Example 1 except that IM32 having a methanol content of 45% by mass was used instead of IM1 having a methanol content of 37.5% by mass in the solvent. A transfer film was prepared.
IM32 made the first curable transparent resin layer cloudy, and the first curable transparent resin layer and the second curable transparent resin layer had insufficient layer fractionation. As a result of subsequent evaluation in the same manner as in Example 1, the visibility of the transparent electrode pattern was significantly deteriorated. The evaluation results are shown in the following table together with other evaluation results. In Comparative Example 4, the crack evaluation and reticulation evaluation of the transfer film, and the patterning property, coloring and substrate adhesion evaluation of the transparent laminate were not performed.

[Comparative Example 5]
In the production of the etching photosensitive film E1 of Example 1, a thermoplastic resin layer having a dry film thickness of 15.1 μm and a dry film thickness of 1. A 6 μm intermediate layer and a first curable transparent resin layer having a dry film thickness of 5 μm were provided. The entire surface was uniformly exposed with an exposure amount of 150 mJ / cm ² (i-line) under a nitrogen atmosphere. Next, the 2nd coating liquid for curable transparent resin layers which consists of IM40 was apply | coated and dried similarly to the above, and the transfer film of the comparative example 5 was produced.
The transfer film of Comparative Example 5 from which the protective film was removed was laminated on the glass transparent substrate obtained above on which a transparent film and a transparent electrode pattern were formed (rubber roller temperature 110 ° C., linear pressure 100 N / cm, conveyance speed 2.0 m / min). The distance between the exposure mask (quartz exposure mask having an overcoat formation pattern) surface and the temporary support is set to 125 μm, and pattern exposure is performed through the temporary support at an exposure amount of 100 mJ / cm ² (i-line). did. After removing the temporary support, a triethanolamine developer (containing 30% by mass of triethanolamine, a trade name: T-PD2 (manufactured by Fuji Film Co., Ltd.) diluted 10 times with pure water) was used. Shower development was carried out at 33 ° C. for 60 seconds with a flat nozzle pressure of 0.1 MPa to remove the thermoplastic resin layer and the intermediate layer. Subsequently, air was blown onto the upper surface of the glass base material to drain the liquid, and then pure water was sprayed for 10 seconds by a shower, pure water shower washing was performed, and air was blown to reduce the liquid pool on the base material.
Thereafter, washing treatment was performed for 60 seconds at 32 ° C. with a 2% aqueous solution of sodium carbonate. However, pattern development of the first and second curable transparent resin layers could not be performed, and the patternability was poor. The front plate after the cleaning treatment was rubbed with a rotating brush, and ultrapure water was sprayed from an ultrahigh pressure cleaning nozzle. Subsequently, air was blown to remove moisture on the base material, and a post-bake treatment at 145 ° C. for 30 minutes was performed. A transparent film, a transparent electrode pattern, a second curable transparent resin layer, A transparent laminate in which one curable transparent resin layer was continued in this order was formed.
Thus, a transparent laminate of Comparative Example 5 was obtained in which a transparent film, a transparent electrode pattern, a second curable transparent resin layer, and a first curable transparent resin layer were laminated in this order on a glass transparent substrate.
In the same manner as in Example 1, the transfer film and the transparent laminate of Comparative Example 5 were evaluated. The results are shown in the table below.

[Comparative Example 6]
In Example 1, it apply | coated and dried similarly using OC1 on the polyethylene terephthalate film (temporary support body), and provided the 1st curable transparent resin layer. Under a nitrogen atmosphere, the entire surface of the first curable transparent resin layer was uniformly exposed with an exposure amount of 150 mJ / cm ² (i-line). Next, the 2nd coating liquid for curable transparent resin layers which consists of IM40 was apply | coated and dried similarly to the above, and the transfer film of the comparative example 6 was produced.
The transfer film of Comparative Example 6 from which the protective film was removed was laminated on the glass transparent substrate obtained in Example 1 above, on which the transparent film and the transparent electrode pattern were formed (rubber roller temperature 110 ° C., wire Pressure 100 N / cm, conveyance speed 2.0 m / min). The distance between the exposure mask (quartz exposure mask having an overcoat formation pattern) surface and the temporary support is set to 125 μm, and pattern exposure is performed through the temporary support at an exposure amount of 100 mJ / cm ² (i-line). did.
Although an attempt was made to peel off the temporary support, it could not be peeled off. The reason is considered as follows.
As in Example 1, the first curable transparent resin layer coating liquid was applied and dried directly on the temporary support, and the first curable transparent resin layer was provided. When the transfer film is prepared by applying and drying, the first curable transparent resin layer is shrunk by exposure when the pattern is exposed through the temporary support and laminated to the substrate as described above. It is considered that the temporary support is easily peeled off. However, in this Comparative Example 6, the first curable transparent resin layer coating solution was applied and dried, then exposed and cured to provide the first curable transparent resin layer, and then the second curable property. A transparent resin layer coating solution is applied and dried to produce a transfer film. At the time of exposure after drying the first curable transparent resin layer, the monomer partially polymerizes, exposure shrinks and accumulates residual stress, but at the time of applying the second curable transparent resin layer coating liquid The first curable transparent resin layer becomes larger by exposure even if it is easily relaxed by the lower alcohol contained in the solvent in the coating solution, and is laminated on the substrate as described above and exposed to pattern through the temporary support. Since the generated residual stress is reduced without shrinking, it is considered that the temporary support is difficult to peel off.
Thus, the transparent laminate of Comparative Example 6 in which the transparent film, the transparent electrode pattern, the second curable transparent resin layer, the first curable transparent resin layer, and the temporary support were laminated in this order on the glass transparent substrate. Obtained. In the same manner as in Example 1, the transfer film and the transparent laminate of Comparative Example 6 were evaluated. The results are shown in the table below. In Comparative Example 6, the crack evaluation and reticulation evaluation of the transfer film, and the transparent electrode pattern visibility, coloring and substrate adhesion evaluation of the transparent laminate were not performed.

[Comparative Example 7]
In Example 1, the second curable transparent resin layer coating liquid IM1 was prepared by using the binder used in IM1 (20% aqueous solution of polyvinyl acetal resin having an acetalization degree of 9 mol% and a hydroxyl group content of 90 mol%, Sekisui Chemical Co., Ltd.) Product name: ESREC KW-1), except that it was changed to a coating solution (IM41) using a 10% aqueous solution of polyvinyl alcohol resin having a saponification degree of 65 mol%, a hydroxyl group content of 65 mol%, and a polymerization degree of polymerization degree of 550. In the same manner as in Example 1, a transfer film and a transparent laminate of Comparative Example 7 were produced and evaluated.
IM41 was cloudy, the first curable transparent resin layer was also clouded, and the layer fraction of the first curable transparent resin layer and the second curable transparent resin layer was insufficient. As a result of subsequent evaluation in the same manner as in Example 1, the visibility of the transparent electrode pattern was significantly deteriorated. The evaluation results are shown in the following table together with other evaluation results.

[Comparative Example 8]
In Example 1, instead of OC1 and IM1, the first photosensitive resin composition solution of Example 1 of JP-A-2005-292734 and the first photosensitive property of Example 1 of JP-A-2005-292734, respectively. The first and second curings were carried out in the same manner as in Example 1 except that the second photosensitive resin composition solution diluted to a solid content of 2.3% by mass without changing the solvent composition ratio of the resin composition solution was used. A transfer film and a transparent laminate of Comparative Example 8 having a conductive transparent resin layer were prepared and evaluated.
When the second photosensitive resin composition solution diluted to a solid content of 2.3% by mass without changing the solvent composition ratio is applied on the first photosensitive resin composition layer, the first curable transparent resin layer Was not dissolved or clouded. However, the boundary between the first curable transparent resin layer and the second curable transparent resin layer was not clear, and the layer fraction was insufficient. The visibility of the transparent electrode pattern also deteriorated. The evaluation results are shown in the following table together with other evaluation results. In Comparative Example 8, the transparent laminate was not evaluated for coloration.

From the said Tables 4-9, it turned out that the transparent laminated body of this invention produced using the transfer film of this invention does not have a problem that a transparent electrode pattern is visually recognized, and patternability is favorable.
On the other hand, from Comparative Examples 1, 2, and 7, the transparent electrode pattern produced by using the transfer film in which the first and second curable transparent resin layers are both water-insoluble layers has a transparent electrode pattern visually recognized. I found out.
In Comparative Example 3 using a transfer film having a refractive index of the second curable transparent resin layer of 1.59 and lower than the range of the present invention, the transparent electrode pattern of the obtained transparent laminate was clearly visible.
From the comparative example 4, it turned out that a transparent electrode pattern will be visually recognized by the transparent laminated body produced using the transfer film with insufficient layer fraction of the 1st and 2nd curable transparent resin layer.
From Comparative Examples 5 and 6, after the first curable transparent resin layer was cured, the transparent laminate produced using the transfer film on which the second curable transparent resin layer was laminated had poor patterning properties. all right.
From Comparative Example 8, the concentration of the first photosensitive resin composition solution of Example 1 of JP-A-2005-292734 is changed so that the first and second curable transparent resin layers are both water-insoluble layers. It was found that when a transfer film was prepared and a transparent laminate was prepared using this transfer film, the transparent electrode pattern would be visually recognized.

[Examples 101 to 135: Production of capacitance-type input device]
(Formation of mask layer)
<Preparation of Photosensitive Film K1 for Forming Mask Layer>
On the polyethylene terephthalate film (temporary support) having a thickness of 75 μm, a coating solution for the thermoplastic resin layer composed of the above-mentioned formulation H1 was applied using a slit nozzle and dried to form a thermoplastic resin layer. . Next, on the thermoplastic resin layer, the intermediate layer coating solution composed of the above-described formulation P1 was applied and dried to form an intermediate layer. Furthermore, the coating liquid for black photocurable resin layers which consists of the following prescription K1 was apply | coated, it was made to dry and the black photocurable resin layer was formed. In this way, the thermoplastic film layer having a dry film thickness of 15.1 μm, the intermediate layer having a dry film thickness of 1.6 μm, and the dry film thickness so that the optical density is 4.0 are formed on the temporary support. A 2.2 μm black photocurable resin layer was provided, and finally a protective film (thickness 12 μm polypropylene film) was pressure-bonded. In this way, a transfer material in which the temporary support, the thermoplastic resin layer, the intermediate layer (oxygen barrier film), and the black photocurable resin layer were integrated was prepared, and the sample name was designated as a mask layer forming photosensitive film K1.

(Coating liquid for black light curable resin layer: Formula K1)
-K pigment dispersion 1: 31.2 parts by mass-R pigment dispersion 1 (the following composition): 3.3 parts by mass-MMPGAc (propylene glycol monomethyl ether acetate, manufactured by Daicel Chemical Industries): 6.2 masses Parts / methyl ethyl ketone (manufactured by Tonen Kagaku): 34.0 parts by mass / cyclohexanone (manufactured by Kanto Denka Kogyo): 8.5 parts by mass / binder 2 (benzyl methacrylate / methacrylic acid = 78/22 molar ratio) Random copolymer, weight average molecular weight 38,000): 10.8 parts by mass Phenothiazine (manufactured by Tokyo Chemical Industry Co., Ltd.): 0.01 parts by mass DPHA (dipentaerythritol hexaacrylate, Nippon Kayaku Co., Ltd.) Propylene glycol monomethyl ether acetate solution (76% by mass): 5.5 parts by mass, 2,4-bis (trichloromethyl) 6- [4 ′-(N, N-bis (ethoxycarbonylmethyl) amino-3′-bromophenyl] -s-triazine: 0.4 part by mass / surfactant (trade name: Megafac F-780F, large (Made by Nippon Ink Co., Ltd.)
: 0.1 mass part In addition, the viscosity of 100 degreeC after the solvent removal of the coating liquid for black photocurable resin layers which consists of the said prescription K1 was 10000 Pa.sec.

(Composition of K pigment dispersion 1)
Carbon black (trade name: Nipex 35, manufactured by Degussa): 13.1% by mass
・ The following dispersant 1: 0.65 mass%
Binder 1 (Random copolymer of benzyl methacrylate / methacrylic acid = 72/28 molar ratio, weight average molecular weight 37,000): 6.72% by mass
Propylene glycol monomethyl ether acetate: 79.53% by mass

-Composition of R pigment dispersion 1-
Pigment (CI Pigment Red 177): 18% by mass
Binder 1 (benzyl methacrylate / methacrylic acid = 72/28 molar ratio random copolymer, weight average molecular weight 37,000): 12% by mass
Propylene glycol monomethyl ether acetate: 70% by mass

<Formation of mask layer>
Next, the glass cleaner liquid adjusted to 25 ° C. was sprayed on a tempered glass (300 mm × 400 mm × 0.7 mm) in which an opening (15 mmΦ) was formed, and was washed with a rotating brush having nylon hair while spraying it for 20 seconds with a shower. After washing with pure water, a silane coupling solution (N-β (aminoethyl) γ-aminopropyltrimethoxysilane 0.3% by mass aqueous solution, trade name: KBM603, manufactured by Shin-Etsu Chemical Co., Ltd.) was showered 20 Sprayed for 2 seconds and washed with pure water shower. This substrate was heated at 140 ° C. for 2 minutes with a substrate preheating device.
The surface of the black photocurable resin layer exposed after removing the protective film from the photosensitive film K1 for mask layer formation obtained from the above to the obtained silane coupling treated glass substrate and the above-mentioned silane coupling Superimposing so that the surface of the treated glass substrate is in contact, using a laminator (manufactured by Hitachi Industries (Lamic II type)), the substrate heated at 140 ° C. as described above, a rubber roller temperature of 130 ° C., Lamination was performed at a linear pressure of 100 N / cm and a conveyance speed of 2.2 m / min. Subsequently, the polyethylene terephthalate temporary support was peeled off at the interface with the thermoplastic resin layer to remove the temporary support. After peeling off the temporary support, the substrate and the exposure mask (quartz exposure mask with a frame pattern) were set up vertically with a proximity type exposure machine (manufactured by Hitachi High-Tech Electronics Engineering Co., Ltd.) having an ultra-high pressure mercury lamp. In this state, the distance between the exposure mask surface and the black light curable resin layer was set to 200 μm, and pattern exposure was performed at an exposure amount of 70 mJ / cm ² (i line).

  Next, using a triethanolamine developer (containing 30% by mass of triethanolamine, trade name: T-PD2 (manufactured by Fuji Film Co., Ltd.) diluted 10 times with pure water) at 33 ° C., 60 ° C. For a second, shower development was performed at a flat nozzle pressure of 0.1 MPa to remove the thermoplastic resin layer and the intermediate layer. Subsequently, air was blown onto the upper surface of the glass base material to drain the liquid, and then pure water was sprayed for 10 seconds by a shower, pure water shower washing was performed, and air was blown to reduce the liquid pool on the base material.

  Thereafter, the shower pressure was reduced to 0.1 MPa at 32 ° C. using a sodium carbonate / sodium hydrogen carbonate developer (trade name: T-CD1 (manufactured by Fuji Film Co., Ltd.) diluted 5 times with pure water). It was set, developed for 45 seconds, and washed with pure water.

  Subsequently, using a surfactant-containing cleaning solution (trade name: T-SD3 (manufactured by Fuji Film Co., Ltd.) diluted 10-fold with pure water) at 33 ° C. for 20 seconds, cone-type nozzle pressure of 0.1 MPa The residue was removed by rubbing the formed pattern image with a rotating brush having soft nylon hairs. Furthermore, ultrapure water was sprayed at a pressure of 9.8 MPa with an ultrahigh pressure washing nozzle to remove residues.

Next, post-exposure is performed in the atmosphere at an exposure amount of 1300 mJ / cm ² , and further post-baking treatment is performed at 240 ° C. for 80 minutes to form a mask layer having an optical density of 4.0 and a thickness of 2.0 μm. A face plate was obtained.

[Transparent film]
A transparent film was formed on the front plate on which the mask layer was formed in the same manner as the transparent film was formed on the glass transparent substrate in the formation of the laminate.

[Formation of first transparent electrode pattern]
<Formation of transparent electrode layer>
A front plate on which a mask layer and a transparent film are formed is introduced into a vacuum chamber, and an ITO target (indium: tin = 95: 5 (molar ratio)) with an SnO ₂ content of 10 mass% is used to form a DC magnetron. A 40 nm thick ITO thin film was formed by sputtering (conditions: substrate temperature 250 ° C., argon pressure 0.13 Pa, oxygen pressure 0.01 Pa) to obtain a front plate on which a transparent electrode layer was formed. The surface resistance of the ITO thin film was 80Ω / □.

<Production of photosensitive film E1 for etching>
In the production of the mask layer forming photosensitive film K1 described above, the mask layer forming photosensitive film was prepared except that the coating solution for black photocurable resin layer was replaced with the coating solution for photocurable resin layer for etching having the following formulation E1. Etching Photosensitive Film E1 was obtained in the same manner as the production of the curable film K1 (the film thickness of the photocurable resin layer for etching was 2.0 μm).

(Coating liquid for photocurable resin layer for etching: prescription E1)
Methyl methacrylate / styrene / methacrylic acid copolymer (copolymer composition (mass%): 31/40/29, weight average molecular weight 60000, acid value 163 mg KOH / g)
: 16 parts by mass-Monomer 1 (Brand name: BPE-500, manufactured by Shin-Nakamura Chemical Co., Ltd.): 5.6 parts by mass-Tetraethylene oxide monomethacrylate 0.5 mol adduct of hexamethylene diisocyanate: 7 parts by mass Cyclohexanedimethanol monoacrylate as a compound having one polymerizable group in the molecule: 2.8 parts by mass, 2-chloro-N-butylacridone: 0.42 parts by mass, 2,2-bis (o-chlorophenyl) ) -4,4 ′, 5,5′-tetraphenylbiimidazole: 2.17 parts by mass Malachite green oxalate: 0.02 parts by mass Leucocrystal violet: 0.26 parts by mass Phenothiazine: 0.013 Part by mass / surfactant (trade name: MegaFuck F-780F, manufactured by Dainippon Ink Co., Ltd.)
: 0.03 parts by mass · methyl ethyl ketone: 40 parts by mass · 1-methoxy-2-propanol: 20 parts by mass In addition, the viscosity at 100 ° C after the solvent removal of the coating solution for photocurable resin layer for etching comprising the above formulation E1 Was 2500 Pa · sec.

<Formation of first transparent electrode pattern>
In the same manner as the formation of the mask layer, the front plate on which the mask layer, the transparent film and the transparent electrode layer were formed was washed, and then the etching photosensitive film E1 from which the protective film was removed was laminated (base material temperature: 130 ° C., Rubber roller temperature 120 ° C., linear pressure 100 N / cm, conveyance speed 2.2 m / min). After peeling off the temporary support, the distance between the exposure mask (quartz exposure mask having a transparent electrode pattern) surface and the photocurable resin layer for etching is set to 200 μm, and the exposure dose is 50 mJ / cm ² (i line). Pattern exposure.
Next, using a triethanolamine developer (containing 30% by mass of triethanolamine, trade name: T-PD2 (manufactured by Fuji Film Co., Ltd.) diluted 10 times with pure water) at 25 ° C., 100 The film was developed for 2 seconds and washed at 33 ° C. for 20 seconds using a surfactant-containing cleaning solution (trade name: T-SD3 (manufactured by FUJIFILM Corporation) diluted 10-fold with pure water). The front plate after the cleaning treatment was rubbed with a rotating brush, and the residue was removed by spraying ultrapure water from an ultrahigh pressure cleaning nozzle. Next, a post-bake treatment at 130 ° C. for 30 minutes was performed to obtain a front plate on which a transparent electrode layer and a photocurable resin layer pattern for etching were formed.

  The front plate on which the transparent electrode layer and the photocurable resin layer pattern for etching are formed is immersed in an etching bath containing ITO etchant (hydrochloric acid, potassium chloride aqueous solution, liquid temperature 30 ° C.) and treated for 100 seconds (etching treatment). Then, the transparent electrode layer in the exposed region that was not covered with the photocurable resin layer for etching was dissolved and removed to obtain a front plate with a transparent electrode layer pattern with the photocurable resin layer pattern for etching.

  Next, a front plate with a transparent electrode layer pattern with a photocurable resin layer pattern for etching was applied to a resist stripping solution (N-methyl-2-pyrrolidone, monoethanolamine, surfactant (trade name: Surfynol 465). , Manufactured by Air Products, Inc., liquid temperature 45 ° C.), immersed in a resist stripping tank, treated for 200 seconds, removed the photocurable resin layer for etching, mask layer, transparent film and first transparent electrode pattern A formed front plate was obtained.

(Formation of insulating layer)
<Preparation of Insulating Layer Forming Photosensitive Film W1>
The production of the mask layer forming photosensitive film K1 is the same as the production of the mask layer forming photosensitive film K1 except that the coating solution for the black light curable resin layer is replaced with an insulating layer coating liquid having the following formulation W1. Thus, a photosensitive film W1 for forming an insulating layer was obtained (the film thickness of the insulating layer was 1.4 μm).

(Insulating layer coating solution: Formula W1)
Binder 3 (cyclohexyl methacrylate (a) / methyl methacrylate (b) / methacrylic acid copolymer (c) glycidyl methacrylate adduct (d) (composition (% by mass): a / b / c / d = 46/1) / 10/43, weight average molecular weight: 36000, acid value 66 mgKOH / g) 1-methoxy-2-propanol, methyl ethyl ketone solution (solid content: 45%)): 12.5 parts by mass DPHA (dipentaerythritol hexaacrylate) Propylene glycol monomethyl ether acetate solution (76% by mass) manufactured by Nippon Kayaku Co., Ltd .: 1.4 parts by mass Urethane monomer (trade name: NK Oligo UA-32P, manufactured by Shin-Nakamura Chemical Co., Ltd .: non-volatile 75% min, propylene glycol monomethyl ether acetate: 25%)
: 0.68 parts by mass · Tripentaerythritol octaacrylate (trade name: V # 802, manufactured by Osaka Organic Chemical Industry Co., Ltd.): 1.8 parts by mass · Diethylthioxanthone: 0.17 parts by mass · 2- (dimethylamino ) -2-[(4-Methylphenyl) methyl] -1- [4- (4-morpholinyl) phenyl] -1-butanone (trade name: Irgacure 379, manufactured by BASF): 0.17 parts by mass Dispersant (product) Name: Solsperse 20000, manufactured by Avicia): 0.19 parts by mass. Surfactant (trade name: Megafac F-780F, manufactured by Dainippon Ink): 0.05 parts by mass, methyl ethyl ketone: 23.3 parts by mass, MMPGAc ( Propylene glycol monomethyl ether acetate (manufactured by Daicel Chemical Industries, Ltd.): 59.8 parts by mass Insulation comprising the above prescription W1 The viscosity at 100 ° C. after removing the solvent from the layer-forming coating solution was 4000 Pa · sec.

In the same manner as the formation of the mask layer, the above-described mask layer, transparent film, and front plate with the first transparent electrode pattern are washed, silane coupled, and then the protective film is removed. W1 was laminated (base material temperature: 100 ° C., rubber roller temperature 120 ° C., linear pressure 100 N / cm, conveyance speed 2.3 m / min). After removing the temporary support, the distance between the exposure mask (quartz exposure mask having the insulating layer pattern) surface and the insulating layer was set to 100 μm, and pattern exposure was performed at an exposure amount of 30 mJ / cm ² (i-line). .

  Next, using a triethanolamine developer (containing 30% by mass of triethanolamine, trade name: T-PD2 (manufactured by Fuji Film Co., Ltd.) diluted 10 times with pure water) at 33 ° C., 60 ° C. Developed for 2 seconds, and further developed at 25 ° C. for 50 seconds using a sodium carbonate / sodium bicarbonate developer (trade name: T-CD1 (manufactured by FUJIFILM Corporation) diluted 5 times with pure water). After the treatment, a washing treatment was performed at 33 ° C. for 20 seconds using a surfactant-containing washing solution (trade name: T-SD3 (manufactured by FUJIFILM Corporation) diluted 10-fold with pure water). The front plate after the cleaning treatment was rubbed with a rotating brush, and the residue was removed by spraying ultrapure water from an ultrahigh pressure cleaning nozzle. Next, a post-baking treatment at 230 ° C. for 60 minutes was performed to obtain a front plate on which a mask layer, a transparent film, a first transparent electrode pattern, and an insulating layer pattern were formed.

[Formation of second transparent electrode pattern]
<Formation of transparent electrode layer>
The front plate on which the mask layer, the transparent film, the first transparent electrode pattern, and the insulating layer pattern are formed is subjected to DC magnetron sputtering in the same manner as the first transparent electrode pattern described above (condition: substrate temperature 50 An ITO thin film having a thickness of 80 nm and an argon pressure of 0.13 Pa and an oxygen pressure of 0.01 Pa was formed to obtain a front plate on which a transparent electrode layer was formed. The surface resistance of the ITO thin film was 110Ω / □.

Similar to the formation of the first transparent electrode pattern, using the etching photosensitive film E1, the mask layer, the transparent film, the first transparent electrode pattern, the insulating layer pattern, the transparent electrode layer, and the etching photocurable resin. A front plate on which a layer pattern was formed was obtained (post-baking treatment; 130 ° C. for 30 minutes).
Furthermore, in the same manner as the formation of the first transparent electrode pattern, etching (30 ° C. for 50 seconds), and then removing the photocurable resin layer for etching (45 ° C. for 200 seconds), the mask layer, the transparent film, A front plate on which the first transparent electrode pattern, the insulating layer pattern, and the second transparent electrode pattern were formed was obtained.

[Formation of conductive elements different from the first and second transparent electrode patterns]
In the same manner as the formation of the first and second transparent electrode patterns described above, the front plate on which the mask layer, the transparent film, the first transparent electrode pattern, the insulating layer pattern, and the second transparent electrode pattern are formed is DC magnetron. A front plate on which an aluminum (Al) thin film having a thickness of 200 nm was formed was obtained by sputtering.

Similar to the formation of the first and second transparent electrode patterns described above, using the photosensitive film E1 for etching, the mask layer, the transparent film, the first transparent electrode pattern, the insulating layer pattern, and the second transparent A front plate on which an electrode pattern and a photocurable resin layer pattern for etching were formed was obtained (post-baking treatment; 130 ° C. for 30 minutes).
Furthermore, in the same manner as the formation of the first transparent electrode pattern, etching (30 ° C. for 50 seconds), and then removing the photocurable resin layer for etching (45 ° C. for 200 seconds), the mask layer, the transparent film, A front plate on which conductive elements different from the first transparent electrode pattern, the insulating layer pattern, the second transparent electrode pattern, and the first and second transparent electrode patterns were formed was obtained.

[First curable transparent resin layer and second curable transparent resin layer]
In the production of the transparent laminate of each example, instead of a substrate on which a transparent film and a transparent electrode pattern are formed on a glass transparent substrate, a mask layer, a transparent film, a first transparent electrode pattern, an insulating layer pattern, a first In the same manner as in the production of the transparent laminate of each of the above examples, except that a front plate on which a conductive element different from the second transparent electrode pattern and the first and second transparent electrode patterns was formed was used. The first curable transparent resin layer and the second curable transparent resin layer are transferred from the transfer film of the example to form a film, and the mask layer, the transparent film, and the first transparent electrode are formed on the glass transparent substrate. Pattern, insulating layer pattern, second transparent electrode pattern, conductive element different from the first and second transparent electrode patterns, second curable transparent resin layer, and first curable transparent resin layer in this order. Capacitive input device of each embodiment formed by To obtain a front plate). The second curable transparent resin layer and the first curable transparent resin layer are patterned and exposed and developed so as not to be formed above the portion where the mask layer is formed and the terminal portion of the routing wiring. It was.

[Production of image display device (touch panel)]
The liquid crystal display element manufactured by the method described in Japanese Patent Application Laid-Open No. 2009-47936 is bonded to the capacitance type input device (front plate) of each of the previously manufactured examples, and the capacitance type input is performed by a known method. The image display apparatus of each Example provided with the apparatus as a component was produced.

<< Evaluation of Front Plate and Image Display Device >>
The capacitance-type input device and the image display device of each example had no problem that the transparent electrode pattern was visually recognized.
In each of the above steps, the mask layer, the transparent film, the first transparent electrode pattern, the insulating layer pattern, the second transparent electrode pattern, a conductive element different from the first and second transparent electrode patterns, the second The front plate on which the curable transparent resin layer and the first curable transparent resin layer are formed has no dirt on the opening and the back surface (non-contact surface), is easy to clean, and has a problem of contamination of other members. There was no.
Also, the mask layer had no pinholes and was excellent in light shielding properties.
And there is no problem in each conductivity of the first transparent electrode pattern, the second transparent electrode pattern, and the conductive element different from these, while the first transparent electrode pattern and the second transparent electrode pattern It had insulation between the transparent electrode patterns.
Furthermore, the first curable transparent resin layer was free from defects such as bubbles and an image display device having excellent display characteristics was obtained.

1 Transparent substrate (front plate)
2 Mask layer 3 Transparent electrode pattern (first transparent electrode pattern)
3a Pad portion 3b Connection portion 4 Transparent electrode pattern (second transparent electrode pattern)
5 Insulating layer 6 Another conductive element 7 First curable transparent resin layer (preferably having a function of an overcoat layer or a transparent protective layer)
8 Opening 10 Capacitive Input Device 11 Transparent Film 12 Second Curable Transparent Resin Layer (Refractive Index Adjusting Layer. May Have Function of Transparent Insulating Layer)
13 Transparent laminate 21 Region 22 in which transparent electrode pattern, second curable transparent resin layer, and first curable transparent resin layer are laminated in this order 22 Non-pattern region α Taper angle 26 Temporary support 29 Protective release layer (protection the film)
30 Transfer film 31 End portion of routing wiring 30 Transfer film 33 Curing portion 34 of first curable transparent resin layer and second curable transparent resin layer Opening corresponding to terminal end of routing wiring (first curable property) (Uncured part of transparent resin layer and second curable transparent resin layer)

Claims (19)

A temporary support, a first curable transparent resin layer, and a second curable transparent resin layer disposed adjacent to the first curable transparent resin layer in this order;
When either one of the first curable transparent resin layer and the second curable transparent resin layer is immersed in water, it exhibits water solubility that completely dissolves within a unit time of 3 minutes / μm per unit film thickness. A layer that is water-insoluble and does not completely dissolve in an immersion time within 3 minutes / μm per unit film thickness when the other is immersed in water,
The refractive index of the second curable transparent resin layer is higher than the refractive index of the first curable transparent resin layer,
A transfer film in which the refractive index of the second curable transparent resin layer is 1.6 or more ;
A transfer film in which the first curable transparent resin layer and the second curable transparent resin layer are fractionated when a cross section of the transfer film is observed with an electron microscope .   The transfer film according to claim 1, wherein the first curable transparent resin layer and the second curable transparent resin layer each independently contain a binder, a polymerizable compound, and a photopolymerizable initiator. The difference between the SP value calculated by the OKITSU method of the binder contained in the water-soluble layer and the SP value calculated by the OKITSU method of the binder contained in the water-insoluble layer is 1.02 The transfer film according to claim 2, which is (MPa) ^1/2 or more.   The transfer film according to claim 2 or 3, wherein the binder contained in the water-soluble layer is a polyvinyl alcohol derivative.   The transfer film according to claim 4, wherein the polyvinyl alcohol derivative is polyvinyl butyral, polyvinyl acetal, fully saponified polyvinyl alcohol, or polyvinyl alcohol obtained by partially saponifying polyvinyl acetate.   The transfer film according to claim 4 or 5, wherein the content of unsubstituted hydroxyl group among the substituted or unsubstituted hydroxyl groups contained in the polyvinyl alcohol derivative is 66 mol% or more.   The transfer film according to any one of claims 1 to 6, wherein the refractive index of the first curable transparent resin layer is 1.50 to 1.53. Transfer film according to any one of claims 1 to 7 the thickness of the second curable transparent resin layer is 500nm or less. Transfer film according to any one of the first curable transparent resin layer of thickness claim 1 which is 1 to 15 m 8. The transfer film according to any one of claims 1 to 9 , wherein the second curable transparent resin layer contains particles having a refractive index of 1.55 or more. Forming a first curable transparent resin layer on the temporary support;
Forming a second curable transparent resin layer directly on the first curable transparent resin layer,
Either one of the first curable transparent resin layer and the second curable transparent resin layer is water / water having an alcohol content of 1 to 3 carbon atoms in a mass ratio of 58/42 to 100/0 or Formed by applying a coating solution containing a mixed solvent, the other formed by applying a coating solution containing an organic solvent,
The refractive index of the second curable transparent resin layer is higher than the refractive index of the first curable transparent resin layer,
The manufacturing method of the transfer film whose refractive index of said 2nd curable transparent resin layer is 1.6 or more. The method for producing a transfer film according to claim 11 , wherein the first curable transparent resin layer and the second curable transparent resin layer each independently contain a binder, a polymerizable compound, and a photopolymerizable initiator. It includes a step of laminating the second curable transparent resin layer and the first curable transparent resin layer of the transfer film according to any one of claims 1 to 10 in this order on a transparent electrode pattern. A method for producing a transparent laminate. The method for producing a transparent laminate according to claim 13 , comprising a step of simultaneously curing the first curable transparent resin layer and the second curable transparent resin layer. The transparent laminated body manufactured with the manufacturing method of the transparent laminated body of Claim 13 or 14 . The transparent electrode pattern further includes a transparent film having a refractive index of 1.6 to 1.78 and a film thickness of 55 to 110 nm on the side opposite to the side on which the second curable transparent resin layer is formed. 15. The transparent laminate according to item 15 . Capacitive input device in which is manufactured using the transfer film according to any one of claims 1-10. Capacitive input device comprising a transparent laminate according to claim 15 or 16. An image display device having as a component a capacitive input device according to claim 17 or 18.

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