JP2001018539A - Thermal transfer recording material - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain a sufficient printing density dealing with an acceleration of a printing speed of thermal transferring by providing a dye layer obtained by blending with a specific pigment dye on a thermal transfer sheet to form the sheet, and blending at least one type of specific plasticizer within an acceptive layer of a thermal transfer image receiving sheet. SOLUTION: The thermal transfer recording material is manufactured by a thermal transfer sheet having a dye layer provided on at least one surface of a base material sheet and a thermal transfer image receiving sheet having an acceptive layer provided on at least one surface of a base material, the dye layer and the acceptive layer are superposed, and a dye in the dye layer is transferred to the acceptive layer by a heating means. In this case, the acceptive layer contains a phenoxy resin, and an yellow dye layer of the dye layer contains at least one type selected from a cellulose ester and a quinophthalon dye represented by the formula (wherein R1 to R5 are each a hydrogen atom, a halogen atom, 1-8C alkyl group or the like, R7, R8 are each a hydrogen atom, an alkyl group, cycloalkyl group or the like).

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a thermal transfer recording material, and more particularly to a thermal transfer recording material, in which a sufficient printing density can be obtained in response to an increase in thermal printing speed, and the reverse side of a thermal transfer sheet during winding storage. When the dye is transferred to the heat-resistant lubricating layer and the transferred dye is unwound, it does not re-transfer to the dye layer of another color or the transferable protective layer and is contaminated. Is related to a thermal transfer recording material obtained.

[0002]

2. Description of the Related Art Various thermal transfer recording methods have been known. Among them, a dye for sublimation transfer is used as a recording material, and the recording material is supported on a base sheet such as a polyester film with an appropriate binder. From a thermal transfer sheet having a dye layer, a sublimation dye is thermally transferred onto a transfer material dyeable with a sublimation dye, for example, a thermal transfer image receiving sheet having a dye receiving layer formed on paper or a plastic film to form various full-color images. A way to do that has been proposed. In this case,
As a heating means, a large number of three- or four-color-adjusted color dots are transferred to the receiving layer of the thermal transfer image-receiving sheet by heating with the thermal head of the printer, and the multicolor dots reproduce the full color of the original. Is what you do. The image formed in this way is very clear and excellent in transparency because the coloring material used is a dye, so the resulting image is excellent in reproducibility and gradation of intermediate colors. It is possible to form a high quality image which is similar to an image by offset printing or gravure printing, and is comparable to a full color photographic image.

[0003]

In recent years, as the printing speed of a thermal transfer printer has been increased, a problem has arisen that a conventional thermal transfer recording material cannot provide a sufficient print density. On the other hand, the dye / resin (Dye / Binder) ratio in the dye layer of the thermal transfer sheet was increased, but the dye was transferred to the heat-resistant lubricating layer on the back side of the thermal transfer sheet during winding storage. When the transferred dye rewinds, it is re-transferred to another color dye layer or transferable protective layer (kickback), and when this contaminated layer is heat-transferred to an image receiving sheet, it may have a different hue from the specified color. , So-called soiling occurs. Although high energy was applied during thermal transfer during image formation, the dye layer and the receptor layer were fused to each other, resulting in so-called abnormal transfer. If a large amount of a release agent is added to the receiving layer to prevent the abnormal transfer, the printing sensitivity is lowered and the printing density is lowered.

As described above, the thermal transfer printer was adjusted and the thermal transfer recording material of the thermal transfer sheet and thermal transfer image receiving sheet used was adjusted in response to the increase in the thermal transfer printing speed. The dye cannot be obtained or is transferred to the heat-resistant lubricating layer on the back side of the thermal transfer sheet during winding storage. And pollute,
Printed materials using the conventional thermal transfer recording materials could not be obtained with satisfactory quality.

Accordingly, an object of the present invention is to provide a sufficient printing density in response to an increase in the printing speed of thermal transfer.
Dye may be transferred to the heat-resistant lubricating layer on the back side of the thermal transfer sheet during winding storage. It is another object of the present invention to provide a thermal transfer recording material from which a printed matter having a sufficiently satisfactory quality can be obtained.

[0006]

Means for Solving the Problems In order to achieve the above object, the present inventors have conducted intensive studies. In a thermal transfer recording material comprising a thermal transfer image-receiving sheet provided with a receiving layer on the surface, a dye layer and a receiving layer are superimposed, and the dye in the dye layer is transferred to the receiving layer by heating means. Among the combinations of the dye and the binder resin of the receiving layer, a combination capable of performing high-sensitivity printing corresponding to the releasability at the time of heating for image formation and increasing the printing speed of thermal transfer was found. It has been reached. If only the thermal transfer sheet is set and the conditions of the thermal transfer image receiving sheet are not asked, and if only the thermal transfer image receiving sheet is set and the conditions of the thermal transfer sheet are not asked, the performance such as mold releasability and high sensitivity is sufficient. Although satisfactory results could not be obtained, satisfactory performance could be exhibited by setting the conditions of the thermal transfer sheet and the thermal transfer image-receiving sheet as a set.

That is, the receptor layer contains a phenoxy resin, and the yellow dye layer of the dye layer comprises a cellulose ester, a quinophthalone-based dye represented by the following general formula (1) and / or the following general formula (2): At least one selected from the dicyanostyryl dyes represented by

[0008]

Embedded image (R ₁ , R ₂ , R ₃ , R ₄ and R ₅ in the above formula can be independently selected, and include a hydrogen atom, a halogen atom C ₁ -C
₈ , an alkyl group, a cycloalkyl group, an alkoxy group, an alkoxyalkoxy group, an alkoxyalkenyl group, a thioalkoxy group, an alkylsulfonyl group, an amino group, a substituted or unsubstituted phenoxy group, or a substituted or unsubstituted thiophenoxy group. Represent. R ₆ and R ₇ can each be independently selected, and include a hydrogen atom, an alkyl group, an alkoxyalkyl group, a cycloalkyl group, an allyl group, an aryl group which may have a substituent, an aralkyl group, a furfuryl group,
Represents a tetrahydrofurfuryl group or a hydroxyalkyl group. )

[0009]

Embedded image(R in the above formula₁Represents an allyl group or an alkyl group;
_TwoRepresents a substituted or unsubstituted alkyl or aryl group.
And A is -CH_Two-, -CH_TwoCH_Two-, -CH _TwoCH
_TwoO-, -CH_TwoCH_TwoOCH_Two-, -CH_TwoCH_TwoO
CH_TwoCH_Two-Represents R_ThreeRepresents an alkyl group. )

Further, the magenta dye layer comprises a cellulose ester and an imidazole azo dye represented by the following general formula (3) and / or a tricyanostyryl dye represented by the following general formula (4) and / or At least one selected from the benzene azo dyes represented by the formula (5)
Contains seeds.

[0011]

Embedded image (R in the above formula represents an alkyl group, an alkenyl group, an aryl group, a cyanoalkyl group, a substituted or unsubstituted alkoxycarbonylalkyl group, and R ₁ and R ₂ represent an alkenyl group, an aralkyl group, or a substituted or unsubstituted group. X represents a hydrogen atom, a methyl group, a methoxy group, a formylamino group, an alkylcarbonylamino group,
Represents an alkylsulfonylamino group or an alkoxycarbonylamino group, and Y represents a hydrogen atom, a methyl group, a methoxy group, or a halogen atom. )

[0012]

Embedded image (R ₁ , R ₂ , and R ₃ in the above formula represent a hydrogen atom, a substituted or unsubstituted alkyl group, an aryl group, an aralkyl group,
Represents an alkenyl group or an alkoxyl group. )

[0013]

Embedded image(R in the above formula is a hydrogen atom, C₁~ C₈An alkyl group of
C₁~ C₈An alkoxy group of C_Three~ C₈The alkoxya
X represents a methyl group or a methoxy group.
Group, formylamino group, C₁~ C₈Alkyl carb
Nylamino group, C ₁~ C₈Of alkylsulfonylamino
Group, C₁~ C₈Of the alkoxycarbonylamino group
And Y is a hydrogen atom, C₁~ C_FourAn alkoxy group, methyl
Represents a group or a halogen atom;₁, R_TwoIs an allyl group, C
₁~ C₈An alkyl group of C_Three~ C₈Alkoxyalkyl
Represents an alkyl group, an aralkyl group, or a hydroxyalkyl group. )

Further, the cyan dye layer has the following general formula (6)
And / or at least a dye represented by the following general formula (7).

[0015]

Embedded image (A in the above formula is a cyano group, an alkoxycarbonyl group,
Represents an aryloxycarbonyl group, a carbamoyl group, an alkylcarbamoyl group, an arylcarbamoyl group, an alkylcarbonyl group, an arylcarbonyl group, an alkylsulfonyl group, an alkylsulfonylamino group, an arylsulfonyl group, or an aryl group, and R ₁ is substituted or unsubstituted Or an atom or atomic group that forms a 5- or 6-membered ring with Z, and R ₂ represents a substituted or unsubstituted alkyl, aralkyl, Or an aryl group, and R ₁ and R ₂ may form a 5- or 6-membered ring which may contain an oxygen atom or a nitrogen atom. R ₃ represents a hydrogen atom, a halogen atom, an optionally substituted alkyl group, an alkoxy group, or an acylamino group, and R ₄ represents a hydrogen atom, a halogen atom, an optionally substituted alkyl group, an alkoxy group. , A nitro group, a cyano group, an acylamino group, or an aryl group; Z represents a hydrogen atom or an atom or an atomic group forming a 5- or 6-membered ring with R ₁ ; Each represents 1 or 2. )

[0016]

Embedded image(Z in the above formula is CN, COOR₁Or CONR_Three
R_FourAnd R₁, R_TwoAnd R_ThreeIs water alone
Alkyl, substituted or unsubstituted alkyl group, substituted or unsubstituted
Substituted cycloalkyl group or substituted or unsubstituted aryl
Or a group represented by R_TwoAnd R_ThreeAre heterocyclic together
The atoms required to close the nucleus or substituted heterocyclic nucleus
And Y is OR_FourOr NR_ThreeR_FourOr CN
R_FourIs hydrogen, a substituted or unsubstituted alkyl group,
Or unsubstituted cycloalkyl group, substituted or unsubstituted ant
Group, SO_ThreeR₇, COR₇, CSR₇Or POR
₇R ₈And R_FiveAnd R₆Is independently R_FourShown in
Having one of the following meanings, or a substituted or unsubstituted amino acid
Or a group represented by R_ThreeAnd R_FourTogether, aliphatic
Or heterocyclic ring containing heterocyclic nucleus having aromatic ring condensation
Atoms required to close the formula or substituted heterocyclic nucleus
And R₇And R₈Are each independently substituted or non-substituted
Substituted alkyl group, substituted or unsubstituted cycloalkyl
Group, substituted or unsubstituted alkenyl group, substituted or unsubstituted
Substituted aralkyl group, substituted or unsubstituted aryl group,
Substituted or unsubstituted alkyloxy group, substituted or unsubstituted
Substituted aryloxy group, substituted or unsubstituted alkylthio
Group, substituted or unsubstituted arylthio group, substituted or
Unsubstituted amino group or substituted or unsubstituted heterocyclic group
Or R₇And R₈Have five members together
X represents an atom necessary for closing a 6-membered ring, and X represents NA
r, N-Het, CR₉R_Ten, N-NR₁₁R₁₂Or N
-N = CR₁₃R₁₄Represents a substituted or unsubstituted
Amino group, substituted or unsubstituted alkyloxy group, also substituted
Or an unsubstituted aryloxy group, substituted or unsubstituted
Alkylthio, substituted or unsubstituted arylthio,
Substitution selected from the group consisting of a droxy group and a mercapto group
Represents an aromatic nucleus substituted in the para position by a group,
Represents a substituted or unsubstituted heterocyclic ring;₉And R_Ten
Are each independently hydrogen, substituted or unsubstituted alkyl
Group, substituted or unsubstituted cycloalkyl group, substituted or unsubstituted
Is an unsubstituted aryl group, substituted or unsubstituted alkenyl
Group, substituted or unsubstituted alkynyl group, substituted or unsubstituted
Substituted heterocyclic ring, cyano group, halogen, SO_ThreeR₇, C
OR₇, CSR₇Or POR₇R₈Or R
₉And R_TenTogether form a substituted or unsubstituted heterocyclic
Necessary for closing a substituted or unsubstituted ring containing a ring
Represents a child, R₁₁Is a substituted or unsubstituted aromatic heterocyclic ring
A substituted or unsubstituted aromatic ring containing₁₂Is R_Four
Has one of the significances indicated for₁₃And R₁₄Is it
Each independently hydrogen, substituted or unsubstituted alkyl group, substituted
Or an unsubstituted cycloalkyl group, or a substituted or
Represents an unsubstituted aryl group, or R₁₃And R₁₄Are together
A heterocyclic nucleus having an aliphatic or aromatic ring condensation
Necessary for ring closure of substituted or unsubstituted heterocyclic nuclei, including
Represents an atom. )

The thermal transfer recording material formed by the combination of the thermal transfer sheet and the thermal transfer image receiving sheet as defined above can provide a sufficient print density in response to the increase in the thermal transfer printing speed, and the back side of the thermal transfer sheet during winding storage. When the dye is transferred to the heat-resistant lubricating layer on the side and the transferred dye is unwound, it does not re-transfer to the dye layer of another color or the transferable protective layer and does not contaminate it. Excellent and satisfactory quality prints can be obtained. A thermal transfer recording material comprising a combination of the above-mentioned yellow dye layer, a magenta dye layer and a cyan dye layer on a substrate sheet, and a thermal transfer image receiving sheet is preferably used. Further, a transferable protective layer is repeatedly provided on the same surface as the surface of the substrate sheet of the thermal transfer sheet on which the dye layer is formed, and the transferable protective layer is transferred to the receiving layer after the dye is transferred to the receiving layer. Is preferably performed. The receiving layer preferably contains at least one selected from phthalic acid plasticizers, phosphate ester plasticizers, polycaprolactone, and polyester plasticizers.

[0018]

DESCRIPTION OF THE PREFERRED EMBODIMENTS Embodiments of the present invention will be described in detail. (Thermal Transfer Sheet) The thermal transfer sheet of the present invention is provided with a dye layer on a base sheet, uses a cellulose ester as a binder resin for the dye layer, and uses a quinophthalone-based dye represented by the general formula (1) as a yellow dye and / or At least one selected from dicyanostyryl dyes of the general formula (2) is used, and the magenta dye is an imidazole azo dye of the above general formula (3) and / or the following general formula (4)
Using a tricyanostyryl dye represented by and / or a benzeneazo dye represented by the following general formula (5),
As the cyan dye, a cyanomethylene dye represented by the general formula (6) and / or a dye represented by the general formula (7) was used. Note that a heat-resistant layer can be provided on the other surface of the base sheet with the thermal transfer sheet in order to prevent sticking of the thermal head and improve slipperiness.

(Substrate Sheet) The substrate sheet may be any one having conventionally known heat resistance and strength to some extent. Thick paper, various processed paper, polyester film, polystyrene film, polypropylene film, polysulfone film, aramid film,
Polycarbonate films, polyvinyl alcohol films, cellophane, etc., and particularly preferred are polyester films. The base sheet as described above,
When the adhesion to the dye layer formed on the surface is poor, it is preferable to perform a primer treatment or a corona discharge treatment on the surface.

The biaxially oriented polyester film used in the present invention is produced by biaxially stretching an unstretched polyethylene-2,6-naphthalate film, heat-fixing the film, and heat-fixing the film. Can be. For example, the unstretched film is stretched in the longitudinal direction at a temperature of Tg to (Tg + 60) ° C., and biaxially stretched in the transverse direction at a magnification of 2 to 6 times.
Heat set at (Tg + 50) ° C. to (Tg + 140) ° C. for 1 to 100 seconds. Stretching can be performed by a method using an IR heater, a roll, a tenter, or the like. The stretching may be performed in the vertical and horizontal directions simultaneously, or may be sequentially performed in the vertical and horizontal directions. In the case where further relaxation treatment is required, the heat treatment is performed before winding on a roll after heat setting. The relaxation treatment method is to reduce the width of the tenter in the middle of the heat fixing zone and reduce the relaxation by 0 to 3% in the film width direction. A method of embedding, a method of separating both end portions of a film, and a method of reducing a take-up speed with respect to a film supply speed under a temperature condition of Tg or more and a melting temperature or less of a film. Heating method, transporting the film on the heating transport roll, reducing the speed of the transport roll after the heating transport roll, taking over the feeding speed than the supply speed while transporting the film on the nozzle that blows out hot air after heat fixing After winding with a film-forming machine,
There is a method in which the film is transported on the heated transport roll and the speed of the transport roll is reduced, and a method in which the roll speed after the heating zone is reduced from the roll speed before the heating zone while transporting the heating zone by a heating oven or an IR heater. Either method may be used, and the relaxation process is performed by setting the deceleration rate of the speed on the take-up side to the speed on the supply side to 0.1 to 3.0%. Further, in order to improve the thermal dimensional stability, in addition to the relaxation treatment, the width of the tenter may be increased in the middle of the heat fixing zone, and a tension treatment of 0 to 3.0% may be performed in the film width direction.

The density of the biaxially oriented polyester film formed as described above is 1.3530 to 1.1. 3600
g / cm < ³ >, and further, 1.3560 to 1.3598 g / c.
m ³ is preferred. If it is smaller than this range, the crystallinity will be small and the thermal dimensional stability will be inferior. If it is larger than this range, the crystallinity will be too large, causing thickness unevenness. When finally obtaining a thermal transfer ribbon, in order to improve the adhesiveness between the base film and the thermal transfer color material layer, after longitudinal stretching, a polyester-based resin or an acrylic-based resin is used alone or by mixing them, and melamine is used. An easy-adhesion layer cured with a system crosslinking agent may be applied. However, the coating amount of the easily adhesive layer was 0.1 g /
cm ² or less, and unevenness in the coating amount is preferably within ± 15% in both the vertical and width directions.

(Dye layer) In the thermal transfer sheet, usually, dye layers of each color of yellow, magenta and cyan are repeatedly provided on a base sheet in a plane-sequential manner.
Magenta and cyan dye layers can be formed one by one on separate base sheets. Further, a thermal transfer sheet having a dye layer of a hue such as black, sepia, green, or gray can be used by combining the dyes used in the dye layers of yellow, magenta, and cyan described below. First, in the yellow dye layer, the quinophthalone-based dye of the general formula (1) and / or the general formula (2)
At least one kind selected from the dicyanostyryl dyes is used.

In the yellow dye layer, the compound represented by the general formula (1)
At least one selected from the group consisting of quinophthalone-based dyes and / or dicyanostyryl-based dyes of the general formula (2) is preferably contained in an amount of at least 30% by weight, more preferably at least 50% by weight of the entire dye. Let it. Further, in the yellow dye layer, in addition to the quinophthalone-based dye and / or the dicyanostyryl-based dye, a conventionally known dye can be used as a yellow dye. In particular, a pyridoneazo-based dye represented by the following general formula (8), It is preferable to use a pyrazolone methine dye represented by the following general formula (9).

[0024]

Embedded image (R ₁ in the above formula is a C ₁ -C ₃ alkyl group, C ₃ -C _{3
8 represents} an alkoxyalkyl group, a cycloalkyl group, an aralkyl group or an allyl group, and R ₂ represents a C ₁ -C ₈ alkyl group, a C ₃ -C ₈ alkoxyalkyl group, a C ₇ -C 8
_{8 represents} an aralkyl group, a cycloalkyl group or an allyl group. )

[0025]

Embedded image (R ₁ and R ₂ in the above formula can be independently selected,
Represents a lower alkyl group which may be substituted, a lower alkenyl group which may be substituted, or an aryl group which may be substituted; and R ₃ and R ₄ may be independently selected and substituted. And a lower alkyl group which may be substituted. )

The magenta dye layer comprises an imidazole azo dye represented by the general formula (3) and / or a tricyanostyryl dye represented by the general formula (4) and / or a benzene azo dye represented by the general formula (5) It contains at least one member selected from among the system dyes. In the magenta dye layer, at least one selected from the group consisting of an imidazole azo dye of the general formula (3) and / or a tricyanostyryl dye of the general formula (4) and / or a benzene azo dye of the general formula (5) is used. The seed is preferably contained in an amount of 30% by weight or more of the entire dye in the magenta dye layer, more preferably 50% by weight or more of the entire dye. Further, in the magenta dye layer, conventionally known dyes as magenta dyes can be used in addition to the above-mentioned imidazole azo dyes and / or tricyanostyryl dyes and / or benzene azo dyes. It is preferable to use a pyrazolotriazole azomethine dye represented by the following or an anthraquinone dye represented by the following general formula (11).

[0027]

Embedded image (R ₁ and R ₂ in the above formula each independently represent a hydrogen atom,
Represents a substituted or unsubstituted alkyl group, vinyl group, allyl group, aryl group, alkoxyalkyl group, aralkyl group, alkoxycarbonylalkyl group, carboxyalkyl group, or alkoxycarboxyalkyl group, wherein R ₁ and R ₂ are May be formed. R ₃ is a hydroxyl group, a halogen atom, a cyano group, a substituted or unsubstituted alkyl group, an alkylformylamino group, an alkylsulfonylamino group, a formylamino group, an allylformylamino group, a sulfonylamino group, an allylsulfonylamino group, a carbamoyl group, Sulfamoyl group, amino group,
Represents a carboxyl group, an alkoxy group or a ureido group, and R ₄ and R ₅ represent a hydrogen atom, a halogen atom, a cyano group, a nitro group, a substituted or unsubstituted alkyl group, an allyl group, a substituted or unsubstituted aryl group, an aralkyl group; Group, alkoxyalkyl group, aralkyloxyalkyl group, thioalkyl group, allyloxyalkyl group, aryloxyalkyl group, carbomoyl group, sulfamoyl group, oxycarbonyl group, amino group, formylamino group, sulfonylamino group, alkoxycarbonylalkyl group, Heterocyclic group, cycloalkyl group, alkylthio group,
Represents an alkylsulfinyl group or an alkylsulfonyl group. )

[0028]

Embedded image (R in the above formula represents a hydrogen atom, an alkyl group, a substituted or unsubstituted aryl group or an alkenyl group, A represents a hydroxyl group or an amino group, X and Y represent a hydrogen atom, an alkyl group,
Represents an alkenyl group or a phenoxy group. )

The cyan dye layer uses a cyanomethylene dye represented by the general formula (6) and / or a dye represented by the general formula (7). Further, in the cyan dye layer, the cyanomethylene dye of the general formula (6) and / or the dye of the general formula (7) is preferably contained in an amount of 30% by weight or more of the total amount of the dye in the cyan dye layer. Of 5
0% by weight or more is contained. Furthermore, in the cyan dye layer,
In addition to the cyanomethylene dye of the general formula (6) and / or the dye of the general formula (7), conventionally known dyes can be used as the cyan dye, and in particular, an anthraquinone-based dye represented by the following general formula (12) It is preferable to use a dye, an indoaniline-based dye represented by the following general formula (13).

[0030]

Embedded image (R ₁ and R ₂ in the above formula represent a hydrogen atom, an alkyl group, a substituted or unsubstituted aryl group, and an alkenyl group;
R ₃ and R ₄ represent a hydrogen atom, an alkyl group, an alkenyl group, or a phenoxy group. )

[0031]

Embedded image (R ₁ in the above formula represents a hydrogen atom, an alkyl group optionally substituted by a fluorine atom, an alkoxy group, a formylamino group, an alkylcarbonylamino group optionally substituted by a fluorine atom, or a halogen atom; R
₂ represents a hydrogen atom, an alkyl group optionally substituted by a fluorine atom, an alkoxy group or a halogen atom,
R ₃ and R ₄ represent an alkyl group, an alkoxy group or a halogen atom which may be substituted by a fluorine atom,
R, R ₅ and R ₆ represent a hydrogen atom, a C _1-6 substituted or unsubstituted alkyl or aryl group. )

The dye layer contains the dye described above and a binder resin mainly composed of cellulose ester. Cellulose esters are produced from esters of cellulose and organic acids, and commercially available ones include CAB, CAP, CA, and the like. It goes without saying that esters and fatty acid esters having 4 or more carbon atoms, for example, esters such as caproic acid and lauric acid can also be used. The molecular weight of the cellulose ester is 10,000 to 70,000 for CAB and 10, CAP for CAP.
000-80,000, CA 30,000-60,0
About 00 is preferable. Further, the degree of esterification is preferably in a range that is soluble in a nonpolar organic solvent such as benzene and toluene. Looking at the degree of esterification of a commercially available cellulose ester, the degree of acetylation is such that the CAB is 2-30.
%, CAP is 0.5 to 3.0%, CA is about 40%, butylation degree is 17 to 60% for CAB, and propionylation degree is about 50% for CAP. Commercially available cellulose esters suitable for the present invention include, for example, cellulose acetate butyrate CA manufactured by Eastman Kodak Company.
B551-a01, CAB551-0.1, CAB55
1-0.2, CAB531-1, CAB500-1, C
AB500-5, CAB553-0.4, CAB381
-0.1, CAB381-0.5, CAB381-0.
5BP, CAB381-2, CAB381-2BP, C
AB381-20, CAB381-20BP, CAB1
71-15S, CAP482-0.5, CAP482-20, CAP for cellulose acetate propionate
504-0.2, CA-39 for cellulose acetate
4-60S, CA-398-3, CA-398-6, C
A-398-10, CA-398-30 and the like.

The proportion of the dye contained in the thermal transfer layer depends on the sublimation (melting) temperature of the dye and the covering power (color rendering) in the color-developed state. Dye / binder ratio) 0.3
The above is preferable, more preferably 0.3 to 3.0, and most preferably 0.55 to 2.5. If the dye / binder ratio is less than 0.3, the image quality such as print density and heat sensitivity is not preferable.

As the binder resin, in addition to the cellulose ester, any conventionally known binder resin can be used in a small amount. Preferred examples thereof include polyvinyl acetal resin, polyvinyl alcohol, polyvinyl acetate, polyvinyl pyrrolidone, and polyacrylamide. And polyester resins.

In order to enhance the releasability from the transfer material at the time of printing, a polysiloxane segment graft-bonded to the main chain of an acrylic, vinyl, polyester, polyurethane, polyamide or cellulose resin, The binder resin for supporting the heat transferable dye may be added to the graft copolymer having at least one type of releasable segment selected from a fluorocarbon segment and a long-chain alkyl segment. The dye layer may contain, as other components, known additives such as a releasing agent, a lubricant, and a filler.

Such a dye layer is prepared by adding the binder resin and the dye and, if necessary, an additive to an appropriate solvent and dissolving or dispersing each component to prepare an ink for forming a dye layer. On the above-mentioned base sheet, for example, it can be formed by applying and drying by a forming means such as a gravure printing method, a screen printing method, and a reverse roll coating method using a gravure plate. The coating thickness of the dye layer is preferably 0.2 μm to 3 μm in a dry state, more preferably 0.3 μm.
m to 2 μm are more preferred.

(Transferable Protective Layer) As the transparent resin layer constituting the transferable resin layer, a resin excellent in friction resistance, transparency, hardness and the like can be appropriately used. Specific examples include polyester resins, polystyrene resins, acrylic resins, polyurethane resins, acrylic urethane resins, vinyl chloride-vinyl acetate copolymer resins, silicone-modified resins of these resins, and mixtures of these resins. Further, a resin or the like obtained by crosslinking and curing an acrylic monomer or the like by irradiation with ionizing radiation can also be used. Specific examples of the acrylic monomer include, for example, ethylene glycol di (meth) acrylate, hexanediol di (meth) acrylate, trimethylolpropane tri (meth) acrylate, trimethylolpropane di (meth) acrylate, and pentaerythritol tetra (meth) acrylate. Examples include acrylate, dipentaerythritol hexa (meth) acrylate, ethylene glycol diglycidyl ether di (meth) acrylate, propylene glycol diglycidyl ether di (meth) acrylate, and sorbitol tetraglycidyl ether tetra (meth) acrylate.

The substance which is cured by ionizing radiation is not limited to the above-mentioned monomer, but may be used as an oligomer.
Further, an acrylic reactive polymer such as polyester acrylate, epoxy acrylate, urethane acrylate, polyether acrylate, or the like comprising a polymer of the above substance or a derivative thereof can also be used. Furthermore, you may mix and use with other acrylic resins. In addition, in consideration of the film breaking property at the time of transfer of these resins, highly transparent fine particles such as silica, alumina, calcium carbonate, and plastic pigments, waxes, and the like may be contained to the extent that transparency is not impaired. In order to improve the rub resistance, gloss, etc. of the image, a lubricant may be contained, and in order to improve the light resistance of the image, a light stabilizer, an antioxidant, an ultraviolet absorber and the like are contained. May be.

The transparent resin layer is prepared by dissolving a resin obtained by adding necessary additives to the resin for the transparent resin layer in a suitable organic solvent or dispersing the dispersion in an organic solvent or water, for example, gravure. It is formed by applying and drying on the above-mentioned substrate film by a forming means such as a coat, a gravure reverse coat and a roll coat. The transparent resin layer can be formed to any thickness, but preferably has a thickness of 0.1 to 50 μm after drying, more preferably 1 to 50 μm.
〜１０10 μm.

Prior to the formation of the transparent resin layer, a release layer may be provided between the base sheet and the transparent resin layer in order to improve the transferability of the transferable resin layer. The release layer is formed from a release agent such as a wax, a silicone wax, a silicone resin, a fluorine resin, an acrylic resin, a polyvinyl alcohol resin, and an ionomer resin. The transparent resin layer can be formed in the same manner as the transparent resin layer, and the thickness after drying is preferably 0.1 to 2 μm. Also, if it is desired that the protective layer after the transfer has been subjected to a matting treatment, by including various particles in the release layer, or by using a substrate sheet having a matte surface,
The surface of the protective layer after the transfer can be made mat-like.

An adhesive layer can be provided on the transparent resin layer in order to improve the transferability of the transferable resin layer.
The adhesive layer is, for example, an acrylic resin, a polyvinyl chloride resin, a polyvinyl acetate resin, a vinyl chloride-vinyl acetate copolymer resin, a polyester resin, a resin having a good adhesive property when heated, such as a polyamide resin. By applying and drying a solution of the resin, it is preferred that the solution be dried.
It is formed to a thickness of 1 to 5 μm.

(Heat-Resistant Layer) The heat-transfer sheet of the present invention as described above is preferably provided with a heat-resistant layer on the back surface thereof in order to prevent adverse effects such as sticking and print wrinkles due to the heat of the thermal head. As the resin for forming the heat-resistant layer, any conventionally known resin may be used. For example, polyvinyl butyral resin, polyvinyl acetoacetal resin, polyester resin, vinyl chloride / vinyl acetate copolymer, polyether resin, polybutadiene resin, Styrene / butadiene copolymer, acrylic polyol, polyurethane acrylate, polyester acrylate, polyether acrylate, epoxy acrylate, urethane or epoxy prepolymer, nitrocellulose resin,
Cellulose nitrate resin, cellulose acetopropionate resin, cellulose acetate butyrate resin,
Examples include cellulose acetate hydrodiene phthalate resin, cellulose acetate resin, aromatic polyamide resin, polyimide resin, polycarbonate resin, chlorinated polyolefin resin, and the like.

Examples of the lubricity-imparting agent to be added to or overcoated with the heat-resistant layer made of these resins include phosphate esters, silicone oils, graphite powders, silicone-based graft polymers, fluorine-based graft polymers, acrylic silicone-grafted polymers, acrylic siloxanes,
Examples thereof include silicone polymers such as arylsiloxanes. Preferably, the layer is a layer composed of a polyol, for example, a polyalcohol polymer compound, a polyisocyanate compound and a phosphate compound, and more preferably a filler is further added.

The heat-resistant layer is prepared by dissolving or dispersing the resin, the lubricity-imparting agent, and the filler described above with an appropriate solvent to prepare an ink for forming a heat-resistant layer. It can be formed on the other surface of the sheet by applying it by a forming means such as a gravure printing method, a screen printing method, or a reverse coating method using a gravure plate, followed by drying.

(Thermal Transfer Image Receiving Sheet) The thermal transfer image receiving sheet of the present invention is provided with a receiving layer on at least one surface of a substrate,
The receiving layer contains a phenoxy resin. As the base material, for example, polyolefin or polystyrene based synthetic paper, high quality paper, art paper, coated paper, cast coated paper, wallpaper, backing paper, synthetic resin or emulsion impregnated paper, synthetic rubber latex impregnated paper, synthetic resin Various plastic films or sheets such as cellulose fiber paper, polyolefin, polyvinyl chloride, polyethylene terephthalate, polystyrene, polymethacrylate, polycarbonate, etc., can be used, and white pigments and fillers can be used in these synthetic resins. A white opaque sheet or a foamed sheet formed by adding an agent to form a film can also be used, and is not particularly limited. Also, a laminate of any combination of the above substrates can be used. The thickness of these substrates may be arbitrary, but is preferably 10 to 300 μm.

The receiving layer formed on the surface of the substrate is for receiving the sublimable dye transferred from the thermal transfer sheet and for maintaining the formed screen, and the receiving layer is formed on at least one surface. In the thermal transfer image-receiving sheet, the receiving layer is formed by having at least a phenoxy resin and one or more plasticizers. The phenoxy resin used in the present invention is a phenoxy resin derived from epichlorohydrin and bisphenol A.
Phenoxy resin modified with a partial hydrolyzate of a polyfunctional silane coupling agent disclosed in JP-A-106393
A modified phenoxy resin in which the hydroxyl group of the phenoxy resin disclosed in JP-A-6-155932 is blocked with an ester group, an amide group, an ether group, or a silyl ether group can also be used.

In addition, other thermoplastic resins other than the phenoxy resin may be blended within a compatible range. The ratio of the resin to be blended is 0 to 100 parts by weight of the phenoxy resin.
If the amount exceeds 100 parts by weight, the density does not correspond to high-speed printing. Thermoplastic resins that can be blended include halogenated polymers such as polyvinyl chloride and polyvinylidene chloride, polyvinyl acetate, ethylene-
Vinyl resins such as vinyl acetate copolymer, vinyl chloride-vinyl acetate copolymer, polyacrylester, polystyrene and polystyrene acryl; acetal resins such as polyvinyl formal, polyvinyl butyral and polyvinyl acetal; and various saturated and unsaturated polyesters Resin,
Examples thereof include a polycarbonate resin, a cellulose resin such as cellulose acetate, a polyolefin resin, and a polyamide resin such as a urea resin, a melamine resin, and a benzoguanamine resin.

The plasticizer used in the present invention includes a phthalic acid plasticizer, a phosphate ester plasticizer, a polycaprolactone, and a polyster plasticizer. The addition amount of the plasticizer depends on the plasticizer, but is preferably 20 to 60 to 70 parts by weight based on 100 parts by weight of the phenoxy resin.
If the amount of the plasticizer is less than 20 parts by weight, there is no density capable of coping with high-speed printing. As a result, a clear image cannot be obtained. In order to obtain sufficient dyeing properties, at least one selected from phthalic acid plasticizers, phosphate ester plasticizers, polycaprolactone, and polyester plasticizers is added to the phenoxy resin.

At present, the thermal transfer recording material described in the present application has a market need of 50% both before and after printing due to the temperature history at the time of product transport and the storage environment after printing (such as in a car in summer). It is required to have a heat resistance of 60C to 60C. Considering the temporal change in recording sensitivity before printing and the bleeding of the image over time during storage after recording, phthalic acid plasticizer, phosphate ester plasticizer, polycaprolactone, melting point of polyester plasticizer, or The freezing point is desirably 60 ° C. or higher.

The phthalic acid plasticizer is represented by the following general formula (14)
Indicated by

Embedded image (However, R ₄ and R ₅ in the formula each represent either an alkyl group or an aryl group.)

Specific examples of the phthalic acid plasticizer include dimethyl phthalate (DMP), diethyl phthalate (DEP), dibutyl phthalate (DBP), dioctyl phthalate (= 2-ethylhexyl phthalate),
Dicyclohexyl phthalate (DCHP), diphenyl phthalate and the like can be mentioned, and DCHP is particularly preferably used.

Next, as the phosphate plasticizer, non-halogen phosphates and non-halogen condensed phosphates represented by the following general formulas (15) and (16) are preferable.

Embedded image [In the above formula 4, R ₁ and R ₂ represent hydrogen, an alkyl group such as a methyl group, or a substituted alkyl group. ]

[0053]

Embedded image [In the above formula 5, R ₁ and R ₂ represent hydrogen, an alkyl group such as a methyl group, or a substituted alkyl group. ]

Regarding polycaprolactone, the number average molecular weight is 2,000 in consideration of bleeding during high-temperature storage after printing.
0 to 100,000, particularly preferably 10,000 to 7
000 is preferred. If the molecular weight is 2,000 or less, it tends to spread over time after recording, and if it is 100,000 or more, there is a problem in the production stability of polycaprolactone itself and the compatibility with the phenoxy resin of the present invention. Further, the polyester plasticizer does not contain polycaprolactone and means a low molecular weight one, and examples thereof include adipic acid polyester and azelaic acid polyester.Diol adipate is particularly effective in improving fingerprint resistance, plasticizer resistance, and the like. Is preferred.

As the release agent used in the receptor layer of the thermal transfer image-receiving sheet of the present invention, an existing release agent can be used, but a fluorine-based surfactant, silicone oil and / or a cured product thereof are particularly preferred. As a fluorine-based surfactant,
Fluorad FC-430, FC-431 (3M
Examples of the silicone oil include various modified silicone oils described in "Silicone Handbook" Nikkan Kogyo Shimbun, and cured products thereof. When the protective layer is transferred and bonded, a fluorine-based surfactant or an uncured silicone oil is preferable so that the protective layer can be bonded.

Further, a conventional release agent may be used in combination with a release agent other than those described above. Even if a plurality of release agents are used, the total amount of the release agent is 0% with respect to the receiving layer resin. .5-
10% by weight is preferred. Various other additives can be added to the receiving layer as needed. In order to improve the whiteness of the receiving layer and further enhance the sharpness of the transferred image,
Pigments and fillers such as titanium oxide, zinc oxide, kaolin, clay, calcium carbonate, and finely divided silica can be added. However, when transparency is required, such as for OHP applications, the amount of the pigment or additive should be such that the required transparency is not lost. In addition, known additives such as a plasticizer, an ultraviolet absorber, a light stabilizer, an antioxidant, a fluorescent brightener, and an antistatic agent can be added to the receiving layer as needed.

The thermal transfer image-receiving sheet of the present invention uses the above-mentioned phenoxy resin on at least one surface of the above-mentioned base material, and is preferably a phthalic acid type plasticizer, a phosphate ester type plasticizer, a polycaprolactone, or a polyester type. Add at least one selected from plasticizers, and further add other necessary additives such as a release agent, a cross-linking agent, a curing agent, a catalyst, an ultraviolet absorber, an antioxidant, and a light stabilizer. Dissolve or disperse what is added appropriately in an appropriate organic solvent, and apply and dry by a forming means such as a gravure printing method, a screen printing method, a reverse roll coating method using a gravure plate to form a dye receiving layer. Obtained by In order to impart antistatic properties, the following antistatic agents can be kneaded into the coating liquid for the receiving layer. Antistatic agents; fatty acid esters, sulfates, phosphates, amides, quaternary ammonium salts, betaines, amino acids, acrylic resins, ethylene oxide adducts and the like. The addition amount of the antistatic agent is 0.1 to
2.0% by weight is preferred.

In the thermal transfer image-receiving sheet of the present invention, the coating amount of the receiving layer is 0.5 g / m ^{2 to} 4.0 g / m ^{2 in} dry weight.
It is preferably ² . Coating amount is 0.5 by dry weight
If it is less than g / m ² , for example, when the receiving layer is provided directly on the base material, the image of the highlight portion becomes rough due to insufficient adhesion with the thermal head due to factors such as the rigidity of the base material. There is a problem. This problem can be avoided by providing an intermediate layer that imparts cushioning properties,
It becomes weak against damage of the receiving layer. Further, the surface roughness when high energy is applied tends to become relatively poor as the coating amount of the receiving layer increases, and when the coating amount exceeds 4.0 g / m ² in dry weight. For example, OHP
In the high-density area at the time of projection, it becomes slightly dark.

In order to improve the adhesion between the substrate and the dye-receiving layer and the cushioning property, an intermediate layer can be provided if necessary. By providing such a cushion layer, an image corresponding to image information can be transferred and formed with good reproducibility without noise during printing. Examples of the intermediate layer resin include a polyester resin, an acrylic resin, a polyurethane resin, butadiene rubber, and an epoxy resin. Further, a lubricating layer can be provided on the back surface of the substrate. Examples of the lubricating layer include acrylic resins such as methyl (meth) acrylate, and vinyl resins such as vinyl chloride-vinyl acetate copolymer. Further, it is possible to provide a detection mark on the thermal transfer image receiving sheet. The detection mark is useful for aligning the thermal transfer sheet and the thermal transfer image receiving sheet and for determining the front and back of the thermal transfer image receiving sheet.
A detection mark that can be detected by the photoelectric tube detection device can be provided on the back surface of the base material by printing or the like.

Examples of applying thermal energy include heating a thermal head and irradiating a laser beam. As a means for applying thermal energy when performing thermal transfer using the above-described thermal transfer sheet and the material to be transferred, any conventionally known applying means can be used. For example, a thermal transfer printer (for example, a video printer VY-100 manufactured by Hitachi, Ltd.) A desired image is formed by applying a thermal energy of about 5 to 100 mJ / mm ² by controlling the recording time with a recording apparatus such as the above.

[0061]

The present invention will be described below in detail with reference to Examples and Comparative Examples. In the description, parts and% are based on weight unless otherwise specified. (Examples 1 to 12) As a substrate sheet, a coating solution for forming a yellow dye layer, a coating solution for forming a magenta dye layer, and a cyan dye layer were formed on one surface of a polyethylene terephthalate film having a thickness of 6 μm. The coating liquid for application was applied and dried by a gravure printing machine so that a yellow dye layer, a magenta dye layer and a cyan dye layer were repeatedly formed on a substrate sheet in a plane-sequential manner. Tables 13, 14 and 15 show combinations of yellow, magenta and cyan dye layer forming coating liquids used in each example. The thermal transfer sheet of the example in which each dye layer had a coating thickness of 1 μm in a dry state was prepared. A heat-resistant layer was provided on the base sheet in advance under the following conditions. On the other surface of the base sheet, a heat-resistant layer ink having the following composition is applied by a gravure printing machine and dried, and a heat-resistant layer having a coating thickness of 1 μm is provided in a dry state, and further oven at 60 ° C. for 5 days. Aging was performed in the medium to perform a curing treatment.

Example 13 A substrate sheet having a thickness of 3
A μm polyethylene naphthalate film was used.
Otherwise, the thermal transfer sheet of Example 13 was prepared in the same manner as the thermal transfer sheet of Example 1 described above.

Coating solution for forming yellow dye layer <Y1> Quinophthalone-based dye (dye shown by chemical formula 24 in Table 1) 3.75 parts Didianostyryl-based dye (dye shown by chemical formula 27 in Table 2) 3.75 parts Cellulose acetate Butyrate 5.0 parts (CAB381-20, manufactured by Eastman Chemical Company) Methyl ethyl ketone / toluene (weight ratio 1/1) 87.5 parts

Coating solution for forming yellow dye layer <Y2> Quinophthalone-based dye (dye shown by chemical formula 25 in Table 1) 2.5 parts Dicyanostyryl dye (dye shown by chemical formula 28 in Table 2) 3.0 parts Pyridoneazo Dye (Dye represented by Chemical Formula 30 in Table 3) 2.0 parts Cellulose acetate butyrate 5.0 parts (CAB381-20, manufactured by Eastman Chemical Company) Methyl ethyl ketone / toluene (weight ratio 1/1) 87.5 parts

Coating solution for forming yellow dye layer <Y3> Quinophthalone dye (dye represented by chemical formula 26 in Table 1) 2.0 parts Dicyanostyryl dye (dye represented by chemical formula 29 in Table 2) 2.0 parts Pyridoneazo 1.5 parts Pyrazolone methine dye (dye represented by Formula 32 in Table 4) 2.0 parts Cellulose acetate butyrate 5.0 parts (CAB381-20, Eastman Chemical Company) Methyl ethyl ketone / toluene (weight ratio 1/1) 87.5 parts

[0066]

[Table 1] (I) in the table means iso-. Also, (n)
Means n-, and those used in the following tables have the same meaning.

[0067]

[Table 2]

[0068]

[Table 3]

[0069]

[Table 4]

Coating solution for forming magenta dye layer <M1> Imidazole azo dye 2.5 parts (dye represented by chemical formula 33 in Table 5) Tricyanostyryl dye 2.5 parts (dye represented by chemical formula 36 in Table 6) 2.5 parts of benzene azo dye (dye represented by chemical formula 39 in Table 7) Cellulose acetate butyrate 5.0 parts (CAB381-20, manufactured by Eastman Chemical Company) Methyl ethyl ketone / toluene (weight ratio 1/1) 87.5 parts

Magenta Dye Layer Forming Coating Solution <M2> Imidazoleazo Dye 3.5 parts (Dye represented by Chemical Formula 34 in Table 5) Tricyanostyryl Dye 2.0 parts (Dye represented by Chemical Formula 37 in Table 6) Benzene azo dye 2.0 parts (dye represented by chemical formula 40 in Table 7) Cellulose acetate butyrate 5.0 parts (CAB381-20, manufactured by Eastman Chemical Company) Methyl ethyl ketone / toluene (weight ratio 1/1) 87.5 parts

Magenta Dye Layer Forming Coating Solution <M3> Imidazoleazo Dye 3.5 parts (Dye represented by Chemical Formula 35 in Table 5) Tricyanostyryl Dye 1.0 part (Dye represented by Chemical Formula 38 in Table 6) 1.5 parts of benzeneazo dye (dye represented by chemical formula 41 in Table 7) 1.5 parts of anthraquinone dye (dye represented by chemical formula 42 in Table 8) 5.0 parts of cellulose acetate butyrate (CAB381-20, Eastman Chemical) Methyl ethyl ketone / toluene (weight ratio 1/1) 87.5 parts

[0073]

[Table 5]

[0074]

[Table 6]

[0075]

[Table 7]

[0076]

[Table 8]

Coating solution for forming cyan dye layer <C1> Cyanomethylene dye (dye represented by chemical formula 44 in Table 9) 3.0 parts Dye represented by general formula (7) (dye represented by chemical formula 47 in Table 10) 4 5.5 parts Cellulose acetate butyrate 5.0 parts (CAB381-20, manufactured by Eastman Chemical) Methyl ethyl ketone / toluene (weight ratio 1/1) 87.5 parts

Cyan Dye Layer Forming Coating Solution <C2> Cyanomethylene dye (dye represented by chemical formula 45 in Table 9) 2.0 parts Dye of general formula (7) (dye represented by chemical formula 48 in Table 10) 4 0.0 parts Anthraquinone dye 1.5 parts (Dye represented by chemical formula 50 in Table 11) Cellulose acetate butyrate 5.0 parts (CAB381-20, manufactured by Eastman Chemical) Methyl ethyl ketone / toluene (weight ratio 1/1) 87. 5 copies

Coating solution for forming cyan dye layer <C3> Cyanomethylene dye (dye represented by chemical formula 46 in Table 9) 1.0 part Dye of general formula (7) (dye represented by chemical formula 49 in Table 10) 4 0.0 part Anthraquinone dye (dye represented by chemical formula 51 in Table 11) 0.5 part Indoaniline dye 2.0 part (dye represented by chemical formula 52 in Table 12) Cellulose acetate butyrate 5.0 parts (CAB381-20 , Manufactured by Eastman Chemical Company) Methyl ethyl ketone / toluene (weight ratio 1/1) 87.5 parts

[0080]

[Table 9]

[0081]

[Table 10]

[0082]

[Table 11]

[0083]

[Table 12]

Ink composition for heat-resistant layer Polyvinyl butyral resin: 3.6 parts ESREC BX-1 polyisocyanate manufactured by Sekisui Chemical Co., Ltd. 8.6 parts Burnock D750 phosphate ester-based lubricating agent manufactured by Dainippon Ink Co., Ltd .: 2 .8 parts Dai Surf Co., Ltd. Plysurf A208S Talc: Nippon Talc Co., Ltd. Microace P-3 0.7 parts Methyl ethyl ketone 32 parts Toluene 32 parts

The thermal transfer sheets of Examples 10 to 12 were provided between the yellow dye layer and the cyan dye layer.
0.5 g / m ² when drying a coating liquid for forming a release layer having the following composition
After coating and drying at a rate of, a coating liquid for forming a transferable protective layer having the following composition was applied and dried at a rate of ² g / m ² at the time of drying. The sheet was provided on the same surface as the surface on which the dye layer was formed.

Coating solution ionomer resin for forming release layer (Chemipearl S659, manufactured by Mitsui Chemicals, Inc.) 10 parts Water / ethanol (2/3 by weight) 100 parts

Coating liquid for forming transferable protective layer : Vinyl chloride-vinyl acetate copolymer 20 parts (Denka vinyl # 1000ALK, manufactured by Denki Kagaku Kogyo KK) Benzotriazole ultraviolet absorber 10 parts (TINUVIN328, CIBA-GEIGY CO.) 80 parts of methyl ethyl ketone / toluene (weight ratio 1/1)

Next, a thermal transfer image-receiving sheet as a transfer material used in the examples was prepared in the following manner. Receptive layer forming coating liquid <R1> Phenoxy resin (PKHH: manufactured by Union Carbide) 80 parts Plasticizer: polyester-based plasticizer (BAA-15: manufactured by Daihachi Chemical Co., Ltd.) 20 parts Release agent: fluorine 3.0 parts of surfactant (Fluorad FC-431: manufactured by 3M) Methyl ethyl ketone / toluene (weight ratio 1/1) 400 parts

Receptive layer forming coating liquid <R2> Phenoxy resin (PKHH: manufactured by Union Carbide Co., Ltd.) 70 parts Plasticizer: polyester plasticizer (BAA-15: manufactured by Daihachi Chemical Co., Ltd.) 30 parts Release Agent: Fluorinated surfactant 3.0 parts (Fluorad FC-431: manufactured by 3M) Methyl ethyl ketone / toluene (weight ratio 1/1) 400 parts

Receptive layer forming coating liquid <R3> Hydroxyl group-blocked phenoxy resin 80 parts Plasticizer: polyester plasticizer (BAA-15: manufactured by Daihachi Chemical Co., Ltd.) 20 parts Release agent: fluorinated surfactant Agent 3.0 parts (Fluorad FC-431: manufactured by 3M) Methyl ethyl ketone / toluene (weight ratio 1/1) 400 parts

The above-mentioned coating solution for forming the receiving layer was coated on synthetic paper (Yupo FPG15 manufactured by Oji Yuka Co., Ltd.)
0) was applied to one surface by a reverse coating method using a gravure plate and dried to prepare a transfer-receiving material. The coating amount is 4.5 g / m ² when dried. The transfer materials used in each embodiment are as shown in Tables 13, 14, and 15 below.

(Comparative Examples 1 to 34) As a base sheet, a coating liquid for forming a yellow dye layer, a coating liquid for forming a magenta dye layer, and a cyan liquid having the following composition were formed on one surface of a polyethylene terephthalate film having a thickness of 6 μm. The coating liquid for forming a dye layer was applied and dried by a gravure printer so that a yellow dye layer, a magenta dye layer, and a cyan dye layer were repeatedly formed on a substrate sheet in a plane-sequential manner. Tables 13, 14 and 15 show combinations of yellow, magenta and cyan dye layer forming coating liquids used in each comparative example. The thermal transfer sheet of the comparative example in which each dye layer had a coating thickness of 1 μm in a dry state was prepared. Further, the heat-resistant layer provided in the example was provided in advance on the base sheet under the same conditions.

Coating solution for forming yellow dye layer <Y4> Quinophthalone dye (dye represented by chemical formula 24 in Table 1) 4.7 parts Dicyanostyryl dye (dye represented by chemical formula 27 in Table 2) 4.7 parts Polyvinyl Acetal resin 3.5 parts (KS-5, manufactured by Sekisui Chemical Co., Ltd.) Methyl ethyl ketone / toluene (weight ratio 1/1) 91.3 parts

Coating solution for forming yellow dye layer <Y5> Quinophthalone dye (dye represented by chemical formula 24 in Table 1) 15 parts Dicyanostyryl dye (dye represented by chemical formula 27 in Table 2) 15 parts Acrylonitrile-styrene copolymer Merged 20 parts (manufactured by Daicel Chemical Industries, Ltd., Sebian JD) Methyl ethyl ketone / toluene (weight ratio 1/1) 50 parts

Yellow Dye Layer Forming Coating Solution <Y6> Quinophthalone Dye (Dye Represented by Chemical Formula 26 in Table 1) 0.7 Part Dicyanostyryl Dye (Dye Represented by Chemical Formula 29 in Table 2) 0.8 Part Bilidonazo Dye (dye represented by chemical formula 31 in Table 3) 3.0 parts Pyrazolone methine dye (dye represented by chemical formula 32 in Table 4) 3.0 parts Cellulose acetate butyrate 5.0 parts (CAB381-20, Eastman Chemical Company) Methyl ethyl ketone / toluene (weight ratio 1/1) 87.5 parts

Yellow Dye Layer Forming Coating Solution <Y7> Quinophthalone Dye (Dye Represented by Chemical Formula 26 in Table 1) 1.0 Part Dicyanostyryl Dye (Dye Represented by Chemical Formula 29 in Table 2) 1.0 Part Pyridoneazo Dye (dye represented by chemical formula 31 in Table 3) 4.0 parts Pyrazolone methine dye (dye represented by chemical formula 32 in Table 4) 4.0 parts Cellulose acetate butyrate 5.0 parts (CAB381-20, Eastman Chemical Company) Methyl ethyl ketone / toluene (weight ratio 1/1) 85 parts

Magenta Dye Layer Forming Coating Solution <M4> Imidazoleazo Dye 1.75 parts (Dye represented by Chemical Formula 33 in Table 5) Tricyanostyryl Dye 1.75 parts (Dye represented by Chemical Formula 36 in Table 6) 1.) Benzeneazo dye 1.75 parts (dye represented by chemical formula 39 in Table 7) Polyvinyl acetal resin 3.5 parts (KS-5, manufactured by Sekisui Chemical Co., Ltd.) Methyl ethyl ketone / toluene (weight ratio 1/1) 3 copies

Magenta Dye Layer Forming Coating Solution <M5> Imidazoleazo Dye 10 parts (Dye shown by Chemical Formula 33 in Table 5) Tricyanostyryl Dye 10 parts (Dye shown by Chemical Formula 36 in Table 6) Benzenazo dye 10 parts (dye represented by chemical formula 39 in Table 7) Acrylonitrile-styrene copolymer 20 parts (Sebian JD, manufactured by Daicel Chemical Industries, Ltd.) Methyl ethyl ketone / toluene (weight ratio 1/1) 50 parts

Magenta Dye Layer Forming Coating Solution <M6> Imidazoleazo Dye 1.0 part (Dye shown by Chemical Formula 35 in Table 5) Tricyanostyryl Dye 0.5 part (Dye shown by Chemical Formula 38 in Table 6) 0.5 parts of benzeneazo dyes (dyes represented by chemical formula 41 in Table 7) 5.5 parts of anthraquinone dyes (dyes represented by chemical formula 43 in Table 8) 5.0 parts of cellulose acetate butyrate (CAB381-20, Eastman Chemical) Methyl ethyl ketone / toluene (weight ratio 1/1) 87.5 parts

Magenta Dye Layer Forming Coating Solution <M7> Imidazoleazo Dye 1.0 part (Dye shown by Chemical Formula 35 in Table 5) Tricyanostyryl Dye 1.5 part (Dye shown by Chemical Formula 38 in Table 6) ) Benzeneazo dye 0.5 part (dye represented by chemical formula 41 in Table 7) Anthraquinone dye 7.0 parts (dye represented by chemical formula 43 in Table 8) Cellulose acetate butyrate 5.0 parts (CAB381-20, Eastman Chemical Methyl ethyl ketone / toluene (weight ratio 1/1) 85 parts

Coating solution for forming cyan dye layer <C4> cyanomethylene dye (dye represented by chemical formula 44 in Table 9) 2.1 parts Dye of general formula (7) 3.15 parts (chemical formula 47 in Table 10) Dyes shown) Polyvinyl acetal resin 3.5 parts (KS-5, manufactured by Sekisui Chemical Co., Ltd.) Methyl ethyl ketone / toluene (weight ratio 1/1) 91.3 parts

Coating solution for forming cyan dye layer <C5> Cyanomethylene dye (dye shown by chemical formula 44 in Table 9) 12 parts Dye of general formula (7) 18 parts (dye shown by chemical formula 47 in Table 10) Acrylonitrile -Styrene copolymer 20 parts (manufactured by Daicel Chemical Industries, Ltd., Sebian JD) methyl ethyl ketone / toluene (weight ratio 1/1) 50 parts

Coating solution for forming cyan dye layer <C6> Cyanomethylene dye (dye shown by chemical formula 46 in Table 9) 0.5 part Dye of general formula (7) (dye shown by chemical formula 49 in Table 10) 1 1.0 part Anthraquinone dye (dye represented by chemical formula 51 in Table 11) 1.0 part Indoaniline dye 5.0 parts (dye represented by chemical formula 53 in Table 12) Cellulose acetate butyrate 5.0 parts (CAB381-20) , Manufactured by Eastman Chemical Company) Methyl ethyl ketone / toluene (weight ratio 1/1) 87.5 parts

Cyan Dye Layer Forming Coating Solution <C7> Cyanomethylene Dye (Dye shown by Chemical Formula 46 in Table 9) 1.0 part Dye of General Formula (7) (Dye shown by Chemical Formula 49 in Table 10) 1 1.0 part Anthraquinone dye (dye represented by chemical formula 51 in Table 11) 1.0 part Indoaniline dye 7.0 parts (dye represented by chemical formula 54 in Table 12) Cellulose acetate butyrate 5.0 parts (CAB381-20 , Manufactured by Eastman Chemical Company) Methyl ethyl ketone / toluene (weight ratio 1/1) 85 parts

The thermal transfer sheets of Comparative Examples 27 to 34 were used.
In between, between the yellow dye layer and the cyan dye layer,
0.5 g of the coating liquid for forming a release layer used in Examples when dried
/ M ^TwoAfter applying and drying at the rate of
The coating liquid for forming the transferable protective layer used in the example was dried at 2 g /
m^TwoApply and dry at a rate of
Turned over and provided on the same surface as the surface on which the dye layer of the base sheet is formed
Was.

Next, a thermal transfer image-receiving sheet as a transfer material used in a comparative example was produced in the following manner. Receptive layer forming coating liquid <R4> Vinyl chloride-vinyl acetate copolymer 70 parts (Denka vinyl # 1000A, manufactured by Denki Kagaku Kogyo KK) Epoxy-modified silicone 10 parts (X-22-3000T, Shin-Etsu Chemical Co., Ltd.) )) Methyl ethyl ketone / toluene (weight ratio 1/1) 400 parts

Receptive layer forming coating liquid <R5> 70 parts of aromatic saturated polyester resin (Vylon 200, manufactured by Toyobo Co., Ltd.) Epoxy-modified silicone 10 parts (X-22-3000T, manufactured by Shin-Etsu Chemical Co., Ltd.) 400 parts of methyl ethyl ketone / toluene (weight ratio 1/1)

The above-mentioned coating solution for forming the receiving layer was coated on a synthetic paper (Yupo FPG15 manufactured by Oji Yuka Co., Ltd.) as a base material.
0) was applied to one surface by a reverse coating method using a gravure plate and dried to prepare a transfer-receiving material. The coating amount is 4.5 g / m ² when dried. The materials to be transferred used in each comparative example are as shown in Tables 13, 14, and 15 below.

Each of the thermal transfer sheets for image formation and above and the thermal transfer image receiving sheet as the transfer material are overlapped with the receiving layer surface as the receiving surface of the transfer material and the dye layer surface of the thermal transfer sheet facing each other.
Thermal transfer recording was performed under the following conditions from the surface of the thermal transfer sheet opposite to the side on which the dye layer was provided in the order of cyan, and gradation images of each color were formed.

(Printing conditions) • Thermal head: KGT-217-12MPL20 (manufactured by Kyocera Corporation) • Heating element average resistance value: 3195 (Ω) • Print density in main scanning direction: 300 dpi • Print density in sub-scanning direction: 300 dpi -Printing power: 0.12 (W / dot)-One line cycle: 5 (msec.)-Printing start temperature: 40 (° C)-Gradation control method: One line cycle is divided into 256 equal parts during one line cycle Using a multi-pulse type test printer capable of varying the number of divided pulses having the determined pulse length from 0 to 255, and setting the duty ratio of each divided pulse to 60%
The number of pulses per line cycle is fixed to 0 at 0 steps, 17 at 1 step, 34 at 2 steps, and the number of pulses per line cycle in increments of 17 from 0 to 255. Controls 16 gradations up to 15 steps.

Transfer of Protective Layer Next, in the printed matter formed as described above,
12 and the thermal transfer sheets of Comparative Examples 27 to 34 each have a transferable protective layer. did.

(Printing conditions) • Thermal head: KGT-217-12MPL20 (manufactured by Kyocera Corporation) • Heating element average resistance: 3195 (Ω) • Print density in the main scanning direction: 300 dpi • Print density in the sub-scanning direction: 300 dpi -Printing power: 0.12 (W / dot)-One line cycle: 5 (msec.)-Printing start temperature: 40 (° C)-Gradation control method: One line cycle is divided into 256 equal parts during one line cycle Using a multi-pulse type test printer capable of varying the number of divided pulses having the determined pulse length from 0 to 255, and setting the duty ratio of each divided pulse to 60%
The number of pulses per line cycle is fixed at 210, solid printing is performed, and the protective layer is transferred to the printing screen.

(Evaluation) Using the prints and the thermal transfer sheet, light fastness, print density and kickback resistance were evaluated for each color unit of yellow, magenta and cyan. The evaluation method is as follows. (Lightfastness) The thermal transfer image-receiving sheet obtained as described above was subjected to thermal transfer recording under the printing conditions described above using the thermal transfer film, and a lightfastness test was performed for each color under the following conditions.

Irradiation tester: Atlas Co. Ci135 Light source: Xenon lamp Filter: IR filter inside, soda lime glass outside Black panel temperature: 45 ° C Irradiation intensity: 1.2 (w / m ² ) ··· 420 nm Irradiation energy: 200 (KJ / m ² ) ··· 420 n
Integrated value in m

For steps where the optical reflection density before irradiation was around 1.0, the change in optical density before and after irradiation was measured, and the residual ratio was calculated by the following equation. Residual rate (%) = ([optical reflection density after irradiation] / [optical reflection density before irradiation]) × 100 Based on this residual rate, light resistance was evaluated according to the following criteria. ：: Residual rate is 80% or more △: Residual rate is 70% or more and less than 80% ×: Residual rate is less than 70%

(Print Density) The thermal transfer image-receiving sheet obtained as described above was subjected to thermal transfer recording under the printing conditions described above using the thermal transfer film, and the optical density was measured.
Evaluation was made according to the following criteria. ：: The optical reflection density is 102% or more in steps near the OD value of 1.0, based on the print density of Comparative Example 21. Δ: When the print density of Comparative Example 21 was set as a reference, the optical reflection density was 98% or more in a step near an OD value of 1.0.
Less than 2%. D: The optical reflection density is less than 98% in steps near the OD value of 1.0, based on the print density of Comparative Example 21.

(Kickback Resistance) In the thermal transfer sheet obtained as described above, the surface of the dye layer of each color and the surface of the heat-resistant layer were overlapped, and the load was 2 kgf / cm ² and the temperature was 50.
The solution was stored at 100 ° C. for 100 hours, and the dye was transferred (kick) to the back surface. The dye is checked for the kickback resistance for each of the colors yellow, magenta, and cyan. That is, the back surface onto which the dye has been transferred is superimposed on the dye layer or the protective layer surface, and the load is 2 kgf / cm ² and the temperature is 6
After storing at 0 ° C. for 4 hours, the dye was transferred (backed) to the surface of the dye layer or the protective layer. The density (O.D.) of the dye layer surface or the protective layer surface before and after the backing of the dye.
D. Value) Macbeth reflection densitometer (Sakata Inx Co., Ltd.)
) And the kickback resistance (ΔO.
D. ) Was evaluated and evaluated according to the following criteria.

ΔO. D. = (OD after backing)
Value)-(OD value before backing) In addition, the OD value is determined by a filter corresponding to the dye to be dye-migrated.
D. The value is measured. Evaluation criteria ：: ΔO. D. ≦ 0.03, the kickback resistance is extremely good. ：: 0.03 <ΔO. D. ≤0.06, good kickback resistance. Δ: 0.06 <ΔO. D. When ≦ 0.09, the kickback resistance is slightly poor. ×: 0.09 <ΔO. D. With poor kickback resistance. The evaluation results are shown in Tables 13, 14, and 15.

[0119]

[Table 13]

[0120]

[Table 14]

[0121]

[Table 15]

[0122]

According to the present invention, as described above, the thermal transfer sheet has a dye layer provided on a base sheet, uses a cellulose ester as a binder resin for the dye layer, and applies the above-mentioned general formula (1) to a yellow dye. ) Quinophthalone dyes and / or
Alternatively, at least one selected from the dicyanostyryl dyes of the general formula (2) is used, and the magenta dye is an imidazole azo dye of the general formula (3) and / or a tricyanostyryl of the general formula (4). And at least one selected from the group consisting of benzeneazo dyes of the general formula (5) and / or the cyanomethylene dye of the general formula (6) and / or the general formula (7) as the cyan dye. Was used. Further, the receiving layer of the thermal transfer image-receiving sheet contains at least one plasticizer selected from phenoxy resin and phthalic acid-based plasticizer, phosphate ester-based plasticizer, polycaprolactone, and polyester-based plasticizer to perform thermal transfer printing. In response to the increase in speed, sufficient print density was obtained, and during transfer and storage, the dye was transferred to the heat-resistant lubricating layer on the back side of the thermal transfer sheet. It does not re-transfer to the dye layer or transferable protective layer, and is not contaminated.
Prints of sufficiently satisfactory quality were obtained.

Continuation of front page (72) Inventor Yoshihiko Tamura 1-1-1, Ichigaya-Kagacho, Shinjuku-ku, Tokyo Inside Dai Nippon Printing Co., Ltd. (72) Inventor Masahiro Hanmura 1-1-1, Ichigaga-cho, Ichigaya, Shinjuku-ku, Tokyo Dai Nippon Printing Co., Ltd. (72) Inventor Nobuyuki Harada 1-1-1, Ichigaya Kagacho, Shinjuku-ku, Tokyo F-term (reference) 2N111 AA01 AA17 AA27 AA47 AA52 BA02 BA03 BA39 BA42 BA44 BA47 BA48 BA49 BA53 CA03 CA30 CA33

Claims (6)

[Claims] 1. A dye on at least one surface of a substrate sheet
A thermal transfer sheet provided with a layer and at least one surface of a substrate
Transfer recording consisting of a thermal transfer image receiving sheet provided with a receiving layer
In the material, the dye layer and the receiving layer are overlapped, and heating means
The dye in the dye layer is transferred to the receptor layer by
The yellow dye layer of the pigment layer is a cellulose ester and
A quinophthalone-based dye represented by the general formula (1) and / or
The dicyanostyryl dye represented by the following general formula (2)
At least one member selected from the group consisting of:
Containing a phenoxy resin
Recording material. Embedded image(R in the above formula₁, R_Two, R_Three, R_FourAnd R_FiveIs it
Hydrogen atom, halogen atom C₁~ C
₈Alkyl group, cycloalkyl group, alkoxy group,
Alkoxyalkoxy group, alkoxycarbonyl group, thio
Alkoxy group, alkylsulfonyl group, amino group, substitution
Or an unsubstituted phenoxy group, or a substituted or unsubstituted
Represents a substituted thiophenoxy group. R₆, R₇Each
Can be independently selected, hydrogen atom, alkyl group, alkoxy
Contains alkyl, cycloalkyl, allyl, and substituents
Aryl group, aralkyl group, furfuryl group,
Tetrahydrofurfuryl group or hydroxyalkyl
Represents a group. )(R in the above formula₁Represents an allyl group or an alkyl group;
_TwoRepresents a substituted or unsubstituted alkyl or aryl group.
And A is -CH_Two-, -CH_TwoCH_Two-, -CH _TwoCH
_TwoO-, -CH_TwoCH_TwoOCH_Two-, -CH_TwoCH_TwoO
CH_TwoCH_Two-Represents R_ThreeRepresents an alkyl group. ) 2. A dye on at least one surface of a substrate sheet
A thermal transfer sheet provided with a layer and at least one surface of a substrate
Transfer recording consisting of a thermal transfer image receiving sheet provided with a receiving layer
In the material, the dye layer and the receiving layer are overlapped, and heating means
The dye in the dye layer is transferred to the receptor layer by
The magenta dye layer of the pigment layer is a cellulose ester and
Imidazole azo dyes represented by the general formula (3) and / or
Or a tricyanostyryl compound represented by the following general formula (4):
Dye and / or benzene represented by the following general formula (5)
It contains an azo dye, and the receiving layer contains a phenoxy resin.
A thermal transfer recording material characterized by containing. Embedded image(R in the above formula represents an alkyl group, an alkenyl group, an aryl
Group, cyanoalkyl group, substituted or unsubstituted alcohol
Represents a xycarbonylalkyl group;₁, R_TwoIs an arche
Nil group, aralkyl group, or substituted or unsubstituted
X represents a hydrogen atom, a methyl group, a methoxy group
Group, formylamino group, alkylcarbonylamino group,
Alkylsulfonylamino group or alkoxycarbo
Y represents a hydrogen atom, a methyl group,
Represents a silyl group or a halogen atom. )(R in the above formula₁, R_Two, R_ThreeIs a hydrogen atom, with substitution
Or unsubstituted alkyl, aryl, aralkyl,
Represents an alkenyl group or an alkoxyl group. )(R in the above formula is a hydrogen atom, C₁~ C₈An alkyl group of
C₁~ C₈An alkoxy group of C_Three~ C₈The alkoxya
X represents a methyl group or a methoxy group.
Group, formylamino group, C₁~ C₈Alkyl carb
Nylamino group, C ₁~ C₈Of alkylsulfonylamino
Group, C₁~ C₈Of the alkoxycarbonylamino group
And Y is a hydrogen atom, C₁~ C_FourAn alkoxy group, methyl
Represents a group or a halogen atom;₁, R_TwoIs an allyl group, C
₁~ C₈An alkyl group of C_Three~ C₈Alkoxyalkyl
Represents an alkyl group, an aralkyl group, or a hydroxyalkyl group. ) 3. A dye on at least one surface of a base sheet.
A thermal transfer sheet provided with a layer and at least one surface of a substrate
Transfer recording consisting of a thermal transfer image receiving sheet provided with a receiving layer
In the material, the dye layer and the receiving layer are overlapped, and heating means
The dye in the dye layer is transferred to the receptor layer by
The cyan dye layer of the material layer is a cellulose ester and the following general
A cyanomethylene dye represented by the formula (6) and / or
Containing a dye represented by the following general formula (7);
Thermal transfer characterized in that the layer contains a phenoxy resin
Recording material. Embedded image(A in the above formula is a cyano group, an alkoxycarbonyl group,
Aryloxycarbonyl, carbamoyl, alkyl
Rucarbamoyl group, arylcarbamoyl group, alkyl
Carbonyl group, arylcarbonyl group, alkylsulfo
Nyl group, alkylsulfonylamino group, arylsulfo
A nyl group or an aryl group;₁Is replaced or
Unsubstituted alkyl, aralkyl, or aryl groups
Or forms a 5- or 6-membered ring with Z
Represents an atom or atomic group that forms_TwoIs replaced or
Unsubstituted alkyl, aralkyl, or aryl groups
And R₁And R_TwoContains oxygen or nitrogen atoms
Alternatively, a 5-membered ring or a 6-membered ring may be formed. R_ThreeIs
Hydrogen atom, halogen atom, alkyl optionally having substituent (s)
R, alkoxy, or acylamino;_FourIs water
Elemental atom, halogen atom, alkyl which may have a substituent
Group, alkoxy group, nitro group, cyano group, acylamino
Group, an aryl group, Z is a hydrogen atom, or
R₁Atoms forming a 5- or 6-membered ring with
Represents an atomic group, and n and m each represent 1 or 2.
You. )(Z in the above formula is CN, COOR₁Or CONR_Three
R_FourAnd R₁, R_TwoAnd R_ThreeIs water alone
Alkyl, substituted or unsubstituted alkyl group, substituted or unsubstituted
Substituted cycloalkyl group or substituted or unsubstituted aryl
Or a group represented by R_TwoAnd R_ThreeAre heterocyclic together
The atoms required to close the nucleus or substituted heterocyclic nucleus
And Y is OR_FourOr NR_ThreeR_FourOr CN
R_FourIs hydrogen, a substituted or unsubstituted alkyl group,
Or unsubstituted cycloalkyl group, substituted or unsubstituted ant
Group, SO_ThreeR₇, COR₇, CSR₇Or POR
₇R ₈And R_FiveAnd R₆Is independently R_FourShown in
Having one of the following meanings, or a substituted or unsubstituted amino acid
Or a group represented by R_ThreeAnd R_FourTogether, aliphatic
Or heterocyclic ring containing heterocyclic nucleus having aromatic ring condensation
Atoms required to close the formula or substituted heterocyclic nucleus
And R₇And R₈Are each independently substituted or non-substituted
Substituted alkyl group, substituted or unsubstituted cycloalkyl
Group, substituted or unsubstituted alkenyl group, substituted or unsubstituted
Substituted aralkyl group, substituted or unsubstituted aryl group,
Substituted or unsubstituted alkyloxy group, substituted or unsubstituted
Substituted aryloxy group, substituted or unsubstituted alkylthio
Group, substituted or unsubstituted arylthio group, substituted or
Unsubstituted amino group or substituted or unsubstituted heterocyclic group
Or R₇And R₈Have five members together
X represents an atom necessary for closing a 6-membered ring, and X represents NA
r, N-Het, CR₉R_Ten, N-NR₁₁R₁₂Or N
-N = CR₁₃R₁₄Represents a substituted or unsubstituted
Amino group, substituted or unsubstituted alkyloxy group, also substituted
Or an unsubstituted aryloxy group, substituted or unsubstituted
Alkylthio, substituted or unsubstituted arylthio,
Substitution selected from the group consisting of a droxy group and a mercapto group
Represents an aromatic nucleus substituted in the para position by a group,
Represents a substituted or unsubstituted heterocyclic ring;₉And R_Ten
Are each independently hydrogen, substituted or unsubstituted alkyl
Group, substituted or unsubstituted cycloalkyl group, substituted or unsubstituted
Is an unsubstituted aryl group, substituted or unsubstituted alkenyl
Group, substituted or unsubstituted alkynyl group, substituted or unsubstituted
Substituted heterocyclic ring, cyano group, halogen, SO_ThreeR₇, C
OR₇, CSR₇Or POR₇R₈Or R
₉And R_TenTogether form a substituted or unsubstituted heterocyclic
Necessary for closing a substituted or unsubstituted ring containing a ring
Represents a child, R₁₁Is a substituted or unsubstituted aromatic heterocyclic ring
A substituted or unsubstituted aromatic ring containing₁₂Is R_Four
Has one of the significances indicated for₁₃And R₁₄Is it
Each independently hydrogen, substituted or unsubstituted alkyl group, substituted
Or an unsubstituted cycloalkyl group, or a substituted or
Represents an unsubstituted aryl group, or R₁₃And R₁₄Are together
A heterocyclic nucleus having an aliphatic or aromatic ring condensation
Necessary for ring closure of substituted or unsubstituted heterocyclic nuclei, including
Represents an atom. ) 4. The yellow dye layer according to claim 1,
A thermal transfer sheet in which the magenta dye layer described in claim 2 and the cyan dye layer described in claim 3 are repeatedly arranged face-to-face on a base sheet, and a thermal transfer image receiving sheet described in claim 1 to 3. A thermal transfer recording material characterized by the following. 5. A transferable protective layer is repeatedly provided on the same surface of the substrate sheet of the thermal transfer sheet on which the dye layer is formed, and the transferable protective layer is transferred to the receiving layer after the dye is transferred to the receiving layer. The thermal transfer recording material according to any one of claims 1 to 4, wherein the thermal transfer recording material is transferred. 6. The method according to claim 1, wherein the receiving layer contains at least one selected from a phthalic acid plasticizer, a phosphate ester plasticizer, a polycaprolactone, and a polyester plasticizer. Item 6. The thermal transfer recording material according to any one of Items 1 to 5.