JPH1195421A - Laser direct lithography type planographic printing plate material - Google Patents

Abstract

PROBLEM TO BE SOLVED: To easily produce a laser direct lithography type planographic printing plate material capable of direct photomechanical processing from digital data by recording with IR laser and excellent in stability during storage without requiring a dispersing process at the time of preparing a coating liq. for a printing plate. SOLUTION: The planographic printing plate material contains a dihydroperimidinesquarylium compd., preferably a compd. represented by formula (1) or (2), or a mixture of such compds. In the formulae (1) and (2), R<1> -R<12> are individually H, alkyl, cycloalkyl, aryl, aralkyl, alkenyl, alkynyl or acyl, adjacent substituents may bond to each other to form a 5- or 6-membered ring, (n) is an integer of 1-6, X<1> -X<3> are individually H or monovalent groups and (m) is an integer of 1-3.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an image recording material that can be used as a lithographic printing plate material, and more particularly to a so-called lithographic printing plate material capable of directly making a plate by using an infrared laser from a digital signal of a computer or the like. About.

[0002]

2. Description of the Related Art Conventionally, as a system for making a plate directly from digital data of a computer, an electrophotographic system, a photopolymerization system for exposing using a laser emitting blue or green light, and a silver salt on a photosensitive resin are known. Laminated ones, silver salt diffusion transfer methods, and the like have been proposed. However, in the case of using the electrophotographic method, the processes of image formation such as charging, exposure, and development are complicated, and the apparatus is complicated and large. In the photopolymerization system, since the plate material is highly sensitive to blue or green light, it is difficult to handle in a bright room. The methods (1), (2), and (3) use silver salts, which makes processing such as development complicated, and of course has the disadvantage of containing silver in the processing waste liquid.

On the other hand, the development of lasers in recent years has been remarkable, and in particular, solid-state lasers and semiconductor lasers that emit infrared light having a wavelength of 760 nm to 1200 nm can be easily obtained with high output and small size. These lasers are very useful as a recording light source when making a plate directly from digital data of a computer or the like.
Laser plate making machines using a semiconductor laser emitting near m and a YAG laser emitting at 1064 nm are commercially available. However, many photosensitive recording materials that are practically useful have a photosensitive wavelength in the visible light range of 760 nm or less.
Images cannot be recorded with these infrared lasers. Therefore, a material that can be recorded by an infrared laser is desired.

[0004] As such a recording material recordable with an infrared laser, a heat-sensitive recording material containing a resol type phenol resin and carbon black disclosed in JP-A-56-69193, and JP-A-7-20629. And a recording material comprising an onium salt, a resol resin, a novolak resin, and an infrared absorber. Also,
JP-A-7-271029 describes a recording material comprising a haloalkyl-substituted s-triazine, a resole resin, a novolak resin, and an infrared absorber. Of the infrared absorbers used for these recording materials, 800 to
Infrared dyes having an absorption in the region around 1200 nm are generally unstable and difficult to use. Although carbon black has no stability problem, it does not dissolve in the coating solvent, so a dispersion step is required when introducing it to the printing plate,
This is disadvantageous in terms of cost, such as complicating the manufacturing process. Also, it was not always easy to form a uniform coating.

[0005]

SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to make a plate directly from digital data of a computer or the like by recording using a solid-state laser and a semiconductor laser that emit infrared light, and furthermore, it is possible to obtain a stable image when storing. An object of the present invention is to provide a laser direct-writing type lithographic printing plate material which has excellent properties, can be easily manufactured without requiring a dispersion step in manufacturing a printing plate coating liquid, and has a uniform coating.

[0006]

The above object has been achieved as a result of diligent studies by using a dihydroperimidine squarylium compound or a mixture thereof as an infrared absorbing dye. The dihydroperimidine squarylium compound is easily dissolved in the coating solution and has excellent storage stability. (I) a laser comprising a dihydroperimidine squarylium compound, preferably a compound represented by the following general formula (1) or a mixture thereof, or a compound represented by the following general formula (2) or a mixture thereof: It is a direct drawing type lithographic printing plate material. General formula (1)

[0007]

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Where R¹, R^Two, R^Three, R^Four, R^Five, R
⁶, R⁷, R⁸, R⁹, R^Ten, R¹¹And R¹²Is it
Hydrogen atom, alkyl group, cycloalkyl group, aryl
Aralkyl, alkenyl, alkynyl or
Represents an acyl group;¹And R ^Two, R^ThreeAnd R^Four, R^FiveAnd R
⁶, R⁷And R⁸, R⁹And R^Ten, R¹¹And R¹², R^TwoWhen
R ^Three, R⁶And R⁷, And R^TenAnd R¹¹Pair selected from
One or more of the combinations are connected to each other and have 5 members
A ring or a 6-membered ring may be formed. n is an integer from 1 to 6
Represents X¹, X^TwoAnd X^ThreeIs a hydrogen atom or 1
And m represents an integer of 1 to 3.

General formula (2)

[0010]

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Where R¹, R^Two, R^Three, R^Four, R^Five, R
⁶, R⁷And R⁸Is a hydrogen atom, an alkyl
Group, cycloalkyl group, aryl group, aralkyl group,
Represents a alkenyl group, an alkynyl group or an acyl group;¹
And R^Two, R^ThreeAnd R^Four, R^FiveAnd R ⁶, R⁷And R⁸, R^TwoWhen
R^Three, And R⁶And R⁷Combination selected from
At least one is bonded to each other to form a 5-membered ring or 6
A member ring may be formed. X¹And X^TwoIs a hydrogen atom
Alternatively, m represents a monovalent group, and m represents an integer of 1 to 3.

(Ii) It further comprises an alkali-soluble binder, an acid generator, and an acid-crosslinkable compound (i).
And a laser direct-drawing lithographic printing plate material described in (1). (iii) The laser direct-drawing lithographic plate according to (i), further comprising an alkali-soluble binder, a substance which is thermally decomposable and substantially degrades the solubility of the alkali-soluble binder when not decomposed. Printing plate material.

Since the above-mentioned dihydroperimidine squarylium compound has an absorption region at a long wavelength (about 800 to 1200 nm), a lithographic printing plate material obtained by using this compound as an infrared absorber can be used as a solid-state laser emitting infrared light. By performing recording using a semiconductor laser, plate making can be performed directly from digital data of a computer or the like. Further, since the compound is a dye, it can be easily produced without requiring a dispersing step in producing a printing plate coating liquid, and the uniformity of the obtained coating film is high. Further, the above compounds have particularly high stability at high temperature and high humidity, and a lithographic printing plate material obtained by using the compound as an infrared absorber has excellent stability during storage.

[0014]

DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail.
First, a dihydroperimidine squarylium compound used in the present invention, preferably a compound represented by the following general formula (1) or (2) will be described. General formula (1)

[0015]

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In the above general formula (1), R¹, R^Two, R^Three,
R^Four, R^Five, R⁶, R⁷, R⁸, R ⁹, R^Ten, R¹¹And
And R¹²Represents a hydrogen atom, an alkyl group,
Kill group, aryl group, aralkyl group, alkenyl group,
A alkynyl group or an acyl group;¹And R^Two, R^ThreeWhen
R^Four, R^FiveAnd R⁶, R⁷And R⁸, R⁹And R^Ten, R¹¹And R
¹², R^TwoAnd R^Three, R⁶And R⁷, And R^TenAnd R¹¹From
One or more of the selected combinations
They may combine to form a 5- or 6-membered ring. n is 1
Represents an integer of from 6 to 6. X¹, X^TwoAnd X^ThreeAre hydrogen sources
And m represents an integer of 1 to 3.

General formula (2)

[0018]

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Where R¹, R^Two, R^Three, R^Four, R^Five, R
⁶, R⁷And R⁸Is a hydrogen atom, an alkyl
Group, cycloalkyl group, aryl group, aralkyl group,
Represents a alkenyl group, an alkynyl group or an acyl group;¹
And R^Two, R^ThreeAnd R^Four, R^FiveAnd R ⁶, R⁷And R⁸, R^TwoWhen
R^Three, And R⁶And R⁷Combination selected from
At least one is bonded to each other to form a 5-membered ring or 6
A member ring may be formed. X¹And X^TwoIs a hydrogen atom
Alternatively, m represents a monovalent group, and m represents an integer of 1 to 3.

Specifically, R ¹ to R ¹² in the general formula (1) and R ¹ to R ⁸ in the general formula (2),
As the alkyl group represented by each (hereinafter, simply represented by “R ¹ to R ¹² ”), an alkyl group having 1 to 20 carbon atoms, more preferably 1 to 12 carbon atoms (for example, methyl,
Ethyl, propyl, butyl, hexyl, undecyl). Further, a halogen atom (for example, F, Cl, B
r), alkoxycarbonyl (eg, methoxycarbonyl, ethoxycarbonyl), hydroxy, alkoxy (eg, methoxy, ethoxy, phenoxy, isobutoxy), carboxyl, sulfo or acyloxy (eg, acetyloxy, butyryloxy, hexylyloxy, benzoyloxy) And so on.
Examples of the cycloalkyl group represented by R ¹ to R ¹² include cyclopentyl and cyclohexyl.
It may be substituted with the substituent described for the alkyl group.

The aryl group represented by R ¹ to R ¹² is preferably an aryl group having 6 to 12 carbon atoms, such as a phenyl group or a naphthyl group. Aryl groups may be substituted. Examples of the substituent include an alkyl group having 1 to 8 carbon atoms (for example, methyl, ethyl and butyl), an alkoxy group having 1 to 6 carbon atoms (for example, methoxy and ethoxy), and an aryloxy group (for example, phenoxy and p-chloro). Phenoxy), halogen atoms (eg, F, Cl,
Br), an alkoxycarbonyl group (for example, methoxycarbonyl, ethoxycarbonyl), a cyano group, a nitro group, a sulfo group, a carboxyl group, a hydroxy group, an amino group, an acylamino group (for example, acetylamino, propionylamino and the like) and an acyloxy group ( For example, acetyloxy, butyryloxy, etc.) are included.

The aralkyl group represented by R ¹ to R ¹² is preferably an aralkyl group having 7 to 12 carbon atoms (eg, benzyl, phenylethyl) and has a substituent (eg, a methyl, methoxy, chloro atom). It may be. R
¹ The alkenyl group represented by R ^12, 2-pentenyl, 2-butenyl, may be mentioned 1-propenyl and 2-propenyl. Examples of the alkynyl group represented by R ¹ to R ¹² include ethynyl and 2-propynyl. Examples of the acyl group represented by R ¹ to R ¹² include acetyl, propionyl, benzoyl, and the like, and may form a ring.
Examples of the monovalent group represented by X ¹ , X ² and X ³ in the general formula ( ¹ ) and X ¹ and X ² in the general formula (2) include the substituents described for the above aryl group. .

In the general formula (1), n is 0 (provided that the above compound in the present invention is a mixture containing, in addition, a compound of n = 1 to 6, preferably n = 1 to 4); Alternatively, it represents an integer of 1 to 6, and each compound may be a single compound or a mixture. In the case of a mixture, n is a mixture of 0 and 1, n is a mixture of 1 and 2, and n is 2
A mixture of 3 and 4, n is a mixture of 3 and 4, n is 0, a mixture of 1 and 2, n is a mixture of 1, 2 and 3, n is 0,
A mixture of 1, 2, and 3, where n is 0, 1, 2, 3, and 4
Any combination such as a mixture of In the case of a mixture, the average value of n is preferably from 1.5 to 3.0. If n is too large, the absorption will increase but the solubility will decrease. If n is too small, the absorption will decrease and the suitability for the laser will decrease.

In the present invention, specific examples of the dihydroperimidine squarylium compound represented by the above formula (1) or (2) which are preferably used are shown below.

[0025]

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[0026]

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[0027]

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[0028]

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[0029]

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In the present invention, the dihydroperimidine squarylium compound represented by the above general formula (1) or (2), which is suitably used, can be synthesized according to the following reaction formula. Further, n in the reaction formula can be adjusted by the charged amount of squaric acid.

[0031]

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In the present invention, the dihydroperimidine squarylium compound represented by the above general formula (1), which is suitably used, can be specifically synthesized as follows.

(Synthesis of Compound 1) 39.6 g of 1,8-diaminonaphthalene, 71.5 g of dipentylcarbonyloxymethyl ketone and 30 mg of sodium p-toluenesulfonate monohydrate were heated and stirred in a steam bath for 3 hours.
After adding 150 ml of methyl alcohol, the precipitated crystals were filtered and 2,2-dipentylcarbonyloxymethyl-2,
97.3 g of 3-dihydroperimidine (a) was obtained. 2.13 g of (a) obtained above, 0.57 g of squaric acid, n
A mixture of 10 ml of butyl alcohol and 10 ml of toluene at an external temperature of 130 ° C. while removing the water formed.
Heated for hours. 20 ml of methyl alcohol was added, and the precipitated crystals were separated by filtration. Thereafter, Compound 1 was fractionated by column chromatography using silica gel and chloroform (yield: 0.5 g, λ _max : 948.2 nm (acetone), ε: 2.19 × 10 ⁵ ).

(Synthesis of Compound 2) 17.5 g of (a) obtained in the above (Synthesis of Compound 1), squaric acid 2.1
g, n-butyl alcohol 100 ml and toluene 1
00 ml of the mixture at an external temperature of 1 while removing the water formed.
The mixture was heated and stirred at 30 ° C. for 3 hours. After allowing to cool, 50 ml of methyl alcohol was added, the crystals were filtered off, and the compound (c) was subjected to column chromatography using silica gel and chloroform.
I got 3.2 g of the compound (c) obtained above, 0.178 g of squaric acid, 30 ml of n-butyl alcohol and 30 ml of toluene were heated at an external temperature of 140 ° C. 30 ml of acetone was added, and the precipitated crystals were separated by filtration and then recrystallized from methylene chloride-acetone to give Compound 2 as 8.
9 g (yield: 0.55 g, λ _max : 1070.5 n)
m (CH ₂ Cl ₂ ), ε: 1.69 × 10 ⁵ ).

(Synthesis of Compound 9) 84.5 g of 2-methyl-2-undecyl-2,3-dihydroperimidine, 22.3 g of squaric acid, 500 ml of n-butyl alcohol
And 500 ml of toluene was heated and stirred at an external temperature of 140 ° C. for 4 hours. The precipitated crystals were separated by filtration and washed with acetone to obtain 50 g of Compound 9. λ _max : 810 nm (1.0),
991.6 nm (1.25), 1120.4 nm (1.
36) 1200 nm (0.9), solvent = CH ₂ C
l ₂ . The numerical value in parentheses is ε, and is shown as a relative value when the absorbance at n = 0 is 1.

In the present invention, the dihydroperimidine squarylium compound suitably used and represented by the above general formula (2) can be specifically synthesized as follows.

(Synthesis of Compound 26) The 2,2-dipentylcarbonyloxymethyl-2,3-dihydroperimidine (a) obtained in the synthesis of Compound 1 was 17.5.
g, squaric acid 2.1 g, n-butyl alcohol 10
A mixture of 0 ml and 100 ml of toluene was heated and stirred at an external temperature of 130 ° C. for 3 hours while removing generated water.
After cooling, 50 ml of methyl alcohol was added, and the precipitated crystals were separated by filtration. Thereafter, compound 26 was obtained by column chromatography using silica gel and chloroform (yield: 10.9 g, λ _max : 796 nm (CH ₂ C
l ₂ ), ε: 1.2 × 10 ⁵ ).

[0038]

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Dihydroperimidine squarylium compounds other than those mentioned in the above synthesis examples can be synthesized in the same manner. Table 1 shows λ _max of the synthesized dihydroperimidine squarylium compound.

[0040]

[Table 1]

The dihydroperimidine squarylium compound used in the present invention is effectively used for a laser direct-writing type lithographic printing plate material, and is particularly useful in the following exemplified systems. Negative-working laser direct-write lithographic printing plate material containing an alkali-soluble binder, an acid generator, and an acid-crosslinkable compound, an alkali-soluble binder, substantially dissolving the alkali-soluble binder when thermally decomposable and not decomposed Positive laser direct drawing type lithographic printing plate material that further contains substances that reduce Laser direct drawing type waterless lithographic printing plate material with a silicone rubber layer, which does not necessarily contain a thermally decomposable compound, but which is exposed to heat by laser so that the exposed area becomes soluble in a developing solution. Lithographic printing plate material.

Next, the materials used in each of the above examples will be described in detail. Examples of the materials used in the above are alkali-soluble binders, acid generators, and acid-crosslinkable compounds.

"Alkali-Soluble Binder" Examples of the alkali-soluble binder used in the present invention include novolak resins, polyhydroxystyrene, and acrylic resins. The novolak resin used in the present invention is a resin obtained by condensing phenols and aldehydes under acidic conditions. Preferred novolak resins include, for example, a novolak resin obtained from phenol and formaldehyde, a novolak resin obtained from m-cresol and formaldehyde, a novolak resin obtained from p-cresol and formaldehyde, a novolak resin obtained from o-cresol and formaldehyde, Novolak resin obtained from octylphenol and formaldehyde, novolak resin obtained from m- / p-mixed cresol and formaldehyde, phenol /
Cresol (o-, m-, p- or m- / p-, m- /
o- or o- / p-mixture) and a novolak resin obtained from formaldehyde. These novolak resins have a weight average molecular weight of 8
With a number average molecular weight of 400-6
000 is preferred.

Examples of the alkali-soluble binder other than the novolak resin used in the present invention include polyhydroxystyrenes, hydroxystyrene-N-substituted maleimide copolymers, hydroxystyrene-maleic anhydride copolymers, and alkali-soluble groups. Acrylic polymer having the same, a urethane type polymer having an alkali-soluble group, and the like. Here, examples of the alkali-soluble group include a carboxyl group, a phenolic hydroxyl group, a sulfonic acid group, a phosphonic acid group, and an imide group.

Also, hydroxystyrene-based polymers such as poly-p-hydroxystyrene, poly-m-hydroxystyrene, p-hydroxystyrene-N-substituted maleimide copolymer and p-hydroxystyrene-maleic anhydride copolymer are used. When used, the weight average molecular weight is 2,000
~ 500,000, and 4,000 ~ 300,00
0 is preferred.

Examples of the acrylic polymer having an alkali-soluble group include methacrylic acid-benzyl methacrylate copolymer, poly (hydroxyphenyl methacrylamide), poly (hydroxyphenylcarbonyloxyethyl acrylate), poly (2,4-dihydroxy Phenylcarbonyloxyethyl acrylate), and the polymers described in Japanese Patent Application No. Hei 8-211731. These acrylic polymers have a weight average molecular weight of 2,000 to 500,000, preferably 4,000 to 500,000.
300,000 are preferred.

Examples of urethane type polymers having an alkali-soluble group include resins obtained by reacting diphenylmethane diisocyanate with hexamethylene diisocyanate, tetraethylene glycol, 2,2-bis (hydroxymethyl) propionic acid, and the like. Among these alkali-soluble polymers, a hydroxystyrene-based polymer and an acrylic copolymer having an alkali-soluble group are preferred from the viewpoint of developability.

In the present invention, these alkali-soluble binders are used in an amount of 10 to 90% by weight, preferably 20 to 85% by weight, particularly preferably 3 to 90% by weight, based on the total solid content of the lithographic printing plate material.
It is used in an amount of 0 to 80% by weight. If the amount of the alkali-soluble polymer compound is less than 10% by weight, the durability of the recording layer is deteriorated, and if it exceeds 90% by weight, it is not preferable in terms of both sensitivity and durability. These alkali-soluble binders may be used alone or in combination of two or more.

[Acid Generator] The acid generator used in the present invention is a compound which generates an acid by heat or light, and is generally a photoinitiator for photocationic polymerization or a photoinitiator for photoradical polymerization. Agents, photochromic agents of pigments, photochromic agents, compounds that generate an acid by known light used in microresist and the like, and mixtures thereof, and the like, which are appropriately selected and used. be able to.

For example, see SISchlesinger, Photogr. Sci.
Eng., 18,387 (1974), TSBal et al., Polymer, 21,4.
Diazonium salts described in U.S. Pat.
Ammonium salts described in 9,055, 4,069,056 and JP-A-3-140,140, DCNecker et al., Macromolecu
les, 17,2468 (1984), CSWen et al., Teh, Proc.Con
f. Rad.Curing ASIA, p478, Tokyo, Oct (1988), U.S. Pat.Nos. 4,069,055, 4,069,056, etc., and phosphonium salts described in JVCrivello et al., Macromolecules, 10
(6), 1307 (1977), Chem. & Eng. News, Nov. 28, p31 (1
988), EP 104,143, U.S. Patent 339,049
No. 410,201, JP-A-2-150,848, JP-A-2-29
No. 6,514, etc., iodonium salts, JVCrivello et
al., Polymer J. 17, 73 (1985), JVCrivello et al.,
J. Org. Chem., 43, 3055 (1978), WRWatt et al., J. Po.
lymer Sci., Polymer Chem. Ed., 22, 1789 (1984), J.
V. Crivello et al., Polymer Bull., 14,279 (1985), J.
V. Crivello et al., Macromolecules, 14 (5), 1141 (198
1), JVCrivello et al., J. Polymer Sci., Polymer C
hem. Ed., 17,2877 (1979), European Patent No. 370,693, U.S. Patent No. 3,902,114, European Patent Nos. 233,567, 297,
443, 297,442; U.S. Patents 4,933,377, 41
0,201, 339,049, 4,760,013, 4,734,44
No. 4, No. 2,833,827, German Patent No. 2,904,626, No. 3,
Sulfonium salts described in JP-A Nos. 604,580 and 3,604,581, JVCrivello et al., Macromolecules, 10 (6), 13
07 (1977), JVCrivello et al., J. Polymer Sci., Pol
selenonium salts described in Ymer Chem. Ed., 17, 1047 (1979), etc., CSWen et al., Teh, Proc. Conf. Rad. Curing
Onium salts such as arsonium salts described in ASIA, p478, Tokyo, Oct (1988), etc.

US Pat. No. 3,905,815, JP-B-46-4605
No., JP-A-48-36281, JP-A-55-32070, JP-A-60-2
39736, JP-A-61-169835, JP-A-61-169837,
JP-A-62-58241, JP-A-62-212401, JP-A-63-702
No. 43, organic halogen compounds described in JP-A-63-298339, etc., K. Meier et al., J. Rad.Curing, 13 (4), 26 (198
6), TPGill et al., Inorg. Chem., 19,3007 (1980),
D. Astruc, Acc. Chem. Res., 19 (12), 377 (1896), organometallics / organic halides described in JP-A-2-14145 and the like,
S. Hayase et al., J. Polymer Sci., 25, 753 (1987), E.
Reichman et al., J. Polymer Sci., Poliymer Chem. E
d., 23, 1 (1985), QQZhu et al., J. Photochem., 36,
85, 39, 317 (1987), B. Amit et al., Tetrahedron Le
tt., (24) 2205 (1973), DHR Barton et al., J. Chem.
Soc., 3571 (1965), PMCollins et al., J. Chem. So
c., Perkin I, 1695 (1975), M. Rudinstein et al., Te
trahedron Lett., (17), 1445 (1975), JWWalker et a
l., J. Am. Chem. Soc., 110, 7170 (1988), SCBusman
et al., J. Imaging Technol., 11 (4), (1985), HMH
oulihan et al., Macromolecules, 21, 2001 (1988), P.
M. Collins et al., J. Chem. Soc., Chem. Commun., 532
(1972), S. Hayase et al., Macromolecules, 18,1799 (1
985), E. Reichmanis et al., J. Electrochem. Soc., So
lid State Sci. Technol., 130 (6), FMHoulihan et
al., Macromolecules, 21, 2001 (1988), EP 029.
0,750, 046,083, 156,535, 271,851
No. 0,388,343, U.S. Pat.Nos. 3,901,710, 4,18
No. 1,531, JP-A-60-198538, JP-A-53-133022, etc., a photoacid generator having a 0-nitrobenzyl-type protecting group, TUNOOKA et al., Polymer Preprints Japan, 35
(8), G. Berner et al., J. Rad. Curing, 13 (4), WJM
ijs et al., Coating Technol., 55 (697), 45 (1983), A
kzo, H. Adachi et al., Polymer Preprints, Japan, 37
(3), European Patent Nos. 0199,672, 84515, and 199,672
No. 044,115, No. 0101,122, U.S. Pat.No. 4,618,55
No. 4, No. 4,371,605, No. 4,431,774, JP-A-64-181
No. 43, compounds disclosed in JP-A-2-245756, JP-A-3-140109, etc., which generate sulfonic acid by photolysis, such as iminosulfonates, and disulfones described in JP-A-61-166544. Compounds can be mentioned.

Compounds in which an acid generator is introduced into the main chain or side chain of a polymer, for example, MEWoodhouse et al., J. Am.
Am. Chem. Soc., 104, 5586 (1982), SPPappas et a
l., J. Imaging Sci., 30 (5), 218 (1986), S. Kondo et.
al., Makromol. Chem. RapidCommun., 9,625 (1988),
Y. Yamada et al., Makromol, Chem. 152, 153, 163 (197
2), JVCrivello et al., J. Polymer Sci., Polymer
Chem. Ed., 17,3845 (1979), U.S. Pat.
No., German Patent No. 3914407, JP-A-63-26653, JP-A-55
-164824, JP-A-62-69263, JP-A-63-14603, JP-A-63-163452, JP-A-62-153853, JP-A-63-146
Compounds described in No. 029 and the like can be used. Furthermore, VNRPillai, Synthesis, (1), 1 (1980), A. Abad
et al., Tetrahedron Lett., (47) 4555 (1971), DHR
Compounds that generate an acid by light described in Barton et al., J. Chem. Soc., (C), 329 (1970), U.S. Pat. No. 3,779,778, and EP 126,712 can also be used.

Among the above compounds which generate an acid by heat or light, those which are particularly effectively used are shown below. (1) The following general formula (PAG) substituted with a trihalomethyl group
The oxazole derivative represented by 1) or the general formula (PAG)
An S-triazine derivative represented by 2).

[0054]

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In the formula, R ¹ represents a substituted or unsubstituted aryl or alkenyl group, R ² represents a substituted or substituted aryl, alkenyl or alkyl group, or —CY ₃ . Y represents a chlorine atom or a bromine atom. Specific examples include the following compounds, but the present invention is not limited thereto.

[0056]

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[0057]

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(2) An iodonium salt represented by the following formula (PAG3) or a sulfonium salt represented by the following formula (PAG4).

[0059]

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In the formula, Ar ¹ and Ar ² each independently represent a substituted or unsubstituted aryl group. Preferred substituents include an alkyl group, a haloalkyl group, a cycloalkyl group,
Aryl group, alkoxy group, nitro group, carboxy group,
Examples include an alkoxycarbonyl group, a hydroxy group, a mercapto group, and a halogen atom. R ³ , R ⁴ and R ⁵ each independently represent a substituted or unsubstituted alkyl group or aryl group. Preferred are an aryl group having 6 to 14 carbon atoms, an alkyl group having 1 to 8 carbon atoms, and substituted derivatives thereof. Preferred substituents are an alkoxy group having 1 to 8 carbon atoms, an alkyl group having 1 to 8 carbon atoms, a nitro group, a carboxyl group, a hydroxy group and a halogen atom for the aryl group, and a substituent for the alkyl group. Carbon number 1
8 is an alkoxy group, a carboxyl group, or an alkoxycarbonyl group.

Z^-Represents a counter anion, for example, B
F_Four, AsF₆ ^-, PF₆ ^-, SbF₆ ^-, Si
F₆ ^2-, ClO_Four ^-, CF_ThreeSO_Three ^-Perfluoro such as
Alkanesulfonic acid anion, pentafluorobenzene
Sulfonic acid anion, naphthalene-1-sulfonic acid ani
Condensed polynuclear aromatic sulfonate anions such as on
Quinone sulfonate anion, 9,10-dimethoxyan
Toracene-2-sulfonic acid anion, containing sulfonic acid group
Dyes and the like can be mentioned, but are not limited to these
is not. Also, R^Three, R^FourAnd R^FiveTwo of them
Ar¹And Ar^TwoIs through each single bond or substituent
May be combined.

Specific examples include the following compounds, but are not limited thereto.

[0063]

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[0064]

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The above onium salts represented by the general formula (PAG3) or (PAG4) are known, and are described, for example, in JWKnap.
czyk et al., J. Am. Chem. Soc., 91, 145 (1969), AL
Maycok et al., J. Org.Chem., 35, 2532, (1970), E. Go
ethas et al., Bull.Soc.Chem.Belg., 73,546, (196
4), HM Leicester, J. Ame.Chem. Soc., 51, 3587 (1
929), JVCrivello et al., J. Polym. Chem. Ed., 1
8,2677 (1980); U.S. Pat.Nos. 2,807,648 and 4,247,47
No. 3, JP-A-53-101,331 and the like. (3) Disulfone derivatives represented by the following general formula (PAG5) or iminosulfonate derivatives represented by the following general formula (PAG6).

[0066]

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Where Ar^ThreeAnd Ar^FourAre replaced independently
Or an unsubstituted aryl group. R ⁶Is replaced or nothing
It represents a substituted alkyl group or an aryl group. A is replacement
Or unsubstituted alkylene group, alkenylene group or aryl
Represents a len group. Specific examples include the compounds shown below.
However, the present invention is not limited to these.

[0068]

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[0069]

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The amount of the acid generator is usually 0.001 to 40% by weight based on the total solid content of the lithographic printing plate material.
Is used in a range of preferably 0.01 to 20% by weight,
More preferably, it is used in the range of 0.1 to 5% by weight.

"Acid-Crosslinkable Compound" The acid-crosslinkable compound used in the present invention refers to a compound which crosslinks in the presence of an acid. For example, a hydroxy-substituted, acetoxymethyl- or alkoxymethyl-substituted compound. Aromatic compounds and heterocyclic compounds which have been used, and a preferable example thereof is a compound obtained by condensing phenols and aldehydes under basic conditions. Preferred among the above compounds are, for example, compounds obtained by condensing phenol and formaldehyde under basic conditions as described above, similarly, compounds obtained from m-cresol and formaldehyde, and compounds obtained from bisphenol A and formaldehyde. And compounds obtained from 4,4′-bisphenol and formaldehyde, and other compounds disclosed as resol resins in GB 2,082,339. These acid crosslinking compounds preferably have a weight average molecular weight of 500 to 100,000 and a number average molecular weight of 200 to 50,000.

Other preferred examples include EP-A No. 0,
An aromatic compound substituted with an alkoxymethyl or oxiranylmethyl group disclosed in U.S. Pat.
P-A No. 0,133,216, DE-A No. 3,63
4,671, monomer and oligomer melamine-formaldehyde condensates and urea-formaldehyde condensates disclosed in DE 3,711,264; alkoxy substitution disclosed in EP-A 0,212,482 Compounds. Still other preferred examples are, for example, melamine-formaldehyde derivatives having at least two free N-hydroxymethyl, N-alkoxymethyl or N-acyloxymethyl groups. Among them, N-
Alkoxymethyl derivatives are particularly preferred. Also, low molecular weight or oligomeric silanols can be used as silicon-containing crosslinkers. Examples of these are dimethyl- and diphenyl-silanediols and oligomers which have already been precondensed and contain these units, for example EP-
No. 0,377,155 can be used.

Among aromatic compounds and heterocyclic compounds poly-substituted with an alkoxymethyl group, the compound has an alkoxymethyl group at a position adjacent to a hydroxyl group, and the alkoxy group of the alkoxymethyl group has 18 or less carbon atoms. Compounds can be mentioned as preferable examples, and particularly preferable examples include compounds represented by the following general formulas (3) to (6).

[0074]

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[0075]

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In the formula, L _{1 to} L ₈ may be the same or different and represent an alkoxymethyl group substituted with an alkoxy group having 18 or less carbon atoms, such as methoxymethyl, ethoxymethyl and the like. These are preferred because they have high crosslinking efficiency and can improve printing durability. The above compounds that are crosslinked by heat may be used alone,
Two or more types may be used in combination. The acid-crosslinkable compound used in the present invention is used in an amount of 5 to 80% by weight, preferably 10 to 75% by weight, particularly preferably 20 to 70% by weight, based on the total solid content of the lithographic printing plate material. .
If the amount of the acid-crosslinkable compound is less than 5% by weight, the durability of the photosensitive layer of the lithographic printing plate material obtained is deteriorated.
Exceeding 0% by weight is not preferred in terms of stability during storage.

Examples of the materials used in the above example include an alkali-soluble binder and a substance which is thermally decomposable and substantially reduces the solubility of the alkali-soluble binder when not decomposed. As the alkali-soluble binder, the compounds described in the above examples can be used as they are.

"Substance which is thermally decomposable and substantially reduces the solubility of the alkali-soluble binder in a state where it is not decomposed" The solubility of the alkali-soluble binder which is thermally decomposable and is not decomposed when used in the present invention As a substance which substantially lowers the above, various onium salts, quinonediazide compounds and the like are excellent in lowering the solubility of the alkali-soluble binder and are preferably used.

Examples of the onium salts include diazonium salts, ammonium salts, phosphonium salts, iodonium salts, sulfonium salts, selenonium salts, arsonium salts and the like. Suitable onium salts used in the present invention include, for example, SI Schlesinger,
Photogr. Sci. Eng., 18,387 (1974), TSBal et a
l., Polymer, 21,423 (1980), JP-A-5-158230
No. 4,069,05
No. 5, 4,069, 056, ammonium salts described in JP-A-3-140140, etc., DCNecker et al., Macromolecules, 1
7,2468 (1984), CSwen et al., Teh, Proc. Conf. Rad.
Curing ASIA, p478, Tokyo, Oct (1988), U.S. Patent No.
Phosphonium salts described in 4,069,055, 4,069,056, etc., JVCrivello et al., Macromolecules, 10 (6), 130
7 (1977), Chem. & Eng. News, Nov. 28, p31 (1988),
European Patent Nos. 104,143, U.S. Patent Nos. 339,049 and 41
No. 0,201, JP-A-2-150848, iodonium salts described in JP-A-2-295514, etc., JVCrivello et al., Polymer
J. 17, 73 (1985), JVCrivello et al., J. Org.
m., 43, 3055 (1978), WRWatt et al., J. Polymer Sc
i., Polymer Chem. Ed., 22, 1789 (1984), JVCrivell
o et al., Polymer Bull., 14,279 (1985), JVCrivell
o etal., Macromolecules, 14 (5), 1141 (1981), JVCr
ivello et al., J. Polymer Sci., Polymer Chem. Ed.,
17,2877 (1979), EP 370,693, U.S. Pat.
902,114; European Patent Nos. 233,567; 297,443;
297,442; U.S. Pat.Nos. 4,933,377; 410,201;
No.339,049, No.4,760,013, No.4,734,444, No.2,8
No. 33,827, German Patent Nos. 2,904,626, 3,604,580
No. 3,604,581, etc., JVCri
vello et al., Macromolecules, 10 (6), 1307 (1977), J.
V. Crivello et al., J. Polymer Sci., Polymer Chem. E
d., 17,1047 (1979) etc., selenonium salts, CSWe
n et al., Teh, Proc. Conf. Rad. Curing ASIA, p478,
Arsonium salts described in Tokyo, Oct (1988) and the like. In the present invention, among these, a diazonium salt is particularly preferred. Particularly preferred diazonium salts include those described in JP-A-5-158230.

Suitable quinonediazide compounds include
An o-quinonediazide compound can be mentioned. The o-quinonediazide compound used in the present invention is a compound having at least one o-quinonediazide group, which increases alkali solubility by thermal decomposition, and can be a compound having various structures. In other words, o-quinonediazide helps the solubility of the light-sensitive material system by both the effect of losing the ability to suppress the dissolution of the alkali-soluble binder due to thermal decomposition and the effect of converting o-quinonediazide itself into an alkali-soluble substance. Examples of the o-quinonediazide compound used in the present invention include those described in J. Am. "Light-Sensitive Systems" by Coser (John Wiley & Son
s. Inc.) pp. 339-352 can be used. Particularly, sulfonate or sulfonamide of o-quinonediazide reacted with various aromatic polyhydroxy compounds or aromatic amino compounds is preferable. is there. Also, benzoquinone- (1,2) -diazide sulfonic acid chloride or naphthoquinone- (1,2) -diazide-5-sulfonic acid chloride and pyrogallol-acetone resin as described in JP-B-43-28403. And benzoquinones described in U.S. Patent Nos. 3,046,120 and 3,188,210.
Esters of (1,2) -diazidesulfonic acid chloride or naphthoquinone- (1,2) -diazide-5-sulfonic acid chloride with a phenol-formaldehyde resin are also suitably used.

Further, esters of naphthoquinone- (1,2) -diazide-4-sulfonic acid chloride with phenol-formaldehyde resin or cresol-formaldehyde resin, naphthoquinone- (1,2) -diazide-4-sulfonic acid chloride and pyrogallol Esters with acetone resins are likewise preferably used. Other useful o-quinonediazide compounds are reported and known in numerous patent-related documents. For example, JP 47-5303, JP 48-63802, JP 48-63803,
JP-A-48-96575, JP-A-49-38701, JP-A-48-13354
No., JP-B-41-11222, JP-B-45-9610, JP-B-49-1
No. 7481, U.S. Pat.Nos. 2,797,213 and 3,454,400,
No. 3,544,323, No. 3,573,917, No. 3,674,495
No. 3,785,825; British Patent No. 1,227,602;
Nos. 1,251,345, 1,267,005, 1,329,888,
No. 1,330,932, and German Patent No. 854,890, etc. can be mentioned. The amount of the o-quinonediazide compound used in the present invention is preferably 1 to 50% by weight, more preferably 5 to 30% by weight, particularly preferably 10 to 30% by weight, based on the total solid content of the lithographic printing plate material. % Range. These compounds can be used alone or as a mixture of several types. If the amount of the o-quinonediazide compound is less than 1% by weight, the recording properties of the image will be deteriorated, while if it exceeds 50% by weight, the durability of the image portion will be deteriorated and the sensitivity will be lowered.

The counter ions of the onium salts include tetrafluoroboric acid, hexafluorophosphoric acid, triisopropylnaphthalenesulfonic acid, 5-nitro-o-toluenesulfonic acid,
-Sulfosalicylic acid, 2,5-dimethylbenzenesulfonic acid, 2,4,6-trimethylbenzenesulfonic acid, 2
-Nitrobenzenesulfonic acid, 3-chlorobenzenesulfonic acid, 3-bromobenzenesulfonic acid, 2-fluorocaprylnaphthalenesulfonic acid, dodecylbenzenesulfonic acid, 1-naphthol-5-sulfonic acid, 2-methoxy-4-hydroxy-5- Benzoyl-benzenesulfonic acid, paratoluenesulfonic acid and the like can be mentioned. Among them, alkyl aromatic sulfonic acids such as hexafluorophosphoric acid, triisopropylnaphthalenesulfonic acid and 2,5-dimethylbenzenesulfonic acid are particularly preferable. The amount of the above compound other than the o-quinonediazide compound is preferably 1 to 50% by weight, more preferably 5 to 30% by weight, particularly preferably 10 to 30% by weight, based on the total solid content of the lithographic printing plate material. Range.

With respect to the examples of the present invention, Japanese Patent Application No. 9-26878, Japanese Patent Application No. 9-26877, Japanese Patent Application No. 9-10755, Japanese Patent Application No. 9-36665, and Japanese Patent Application No. No. 9-89451, Japanese Patent Application Nos. 9-85328 and 9-89816, a system using a polymer compound having a functional group capable of generating sulfonic acid in a side chain, WO
-9635143, US-5506090, EP-65
2483, EP-703499, US-555226
0, a system using a carboxylic acid polymer protected with an acid-decomposable group, disclosed in EP-600615. For example, there is a photosensitive lithographic printing plate which does not require dampening solution and has a silicone rubber layer provided on a photosensitive material similar to that disclosed in Japanese Patent Application No. 7-277889.
With respect to the examples described in JP-B-46-27919, a polymer compound or a composition which is insoluble or slightly soluble before heating and which can be made more soluble in a solvent under the influence of heat is incorporated. The use of a recording material that has been used.

[Other Components] The lithographic printing plate material of the present invention may contain various compounds other than those described above, if necessary. For example, a dye having a large absorption in the visible light region can be used as a colorant for an image. Specifically, Oil Yellow # 101, Oil Yellow # 103, Oil Pink # 312, Oil Green BG, Oil Blue BOS, Oil Blue # 603, Oil Black BY,
Oil Black BS, Oil Black T-505 (all manufactured by Orient Chemical Industries, Ltd.), Victoria Pure Blue, Crystal Violet (CI42555), Methyl Violet (CI42535), Ethyl Violet, Rhodamine B (CI145170B), Malachite Green (CI42000) , Methylene blue (CI5
2015) or the dyes described in JP-A-62-293247. These dyes are preferably added because the image area and the non-image area can be easily distinguished after image formation. The addition amount is
0.01 to 10% by weight based on the total solid content of the lithographic printing plate material
Is the ratio of

In the lithographic printing plate material according to the present invention, Japanese Patent Application Laid-Open No. 62-251740 and Japanese Patent Application Laid-Open No. 3-208514 are used in order to increase the stability of processing under development conditions.
Non-ionic surfactants described in JP-A-59-121044, JP-A-4-13149.
An amphoteric surfactant such as that described in JP-A No. 2-211 can be added. Specific examples of the nonionic surfactant include sorbitan tristearate, sorbitan monopalmitate, sorbitan triolate, monoglyceride stearic acid, and polyoxyethylene nonyl phenyl ether. Specific examples of the surfactant include alkyl di (aminoethyl) glycine, alkyl polyaminoethyl glycine hydrochloride, 2-alkyl-N-carboxyethyl-N-hydroxyethylimidazolinium betaine and N-tetradecyl-N, N-betaine. Type (for example,
(Trade name: Amogen K, manufactured by Dai-ichi Kogyo Co., Ltd.). The proportion of the nonionic surfactant and the amphoteric surfactant in the lithographic printing plate material is 0.05 to 15% by weight.
And more preferably 0.1 to 5% by weight.

Further, a plasticizer may be added to the planographic printing plate material according to the present invention, if necessary, in order to impart flexibility to the coating film. For example, butyl phthalyl, polyethylene glycol, tributyl citrate, diethyl phthalate, dibutyl phthalate, dihexyl phthalate, dioctyl phthalate, tricresyl phosphate, tributyl phosphate, trioctyl phosphate, tetrahydrofurfuryl oleate, acrylic acid or Oligomers and polymers of methacrylic acid are used.

Other than these, the above-mentioned onium salts, haloalkyl-substituted s-triazines, epoxy compounds, vinyl ethers, and further, Japanese Patent Application No. 7-18120.
Phenol compounds having a hydroxymethyl group and phenol compounds having an alkoxymethyl group.

The lithographic printing plate material according to the present invention can be usually produced by dissolving each of the above-mentioned components in a solvent and applying it on a suitable support. As the solvent used here, ethylene dichloride, cyclohexanone,
Methyl ethyl ketone, methanol, ethanol, propanol, ethylene glycol monomethyl ether, 1-
Methoxy-2-propanol, 2-methoxyethyl acetate, 1-methoxy-2-propyl acetate, dimethoxyethane, methyl lactate, ethyl lactate, N, N-dimethylacetamide, N, N-dimethylformamide, tetramethylurea, N- Examples thereof include, but are not limited to, methylpyrrolidone, dimethyl sulfoxide, sulfolane, γ-butyl lactone, toluene, water and the like. These solvents are used alone or as a mixture. The concentration of the above components (total solids including additives) in the solvent is preferably 1 to 50% by weight. The amount of coating (solid content) on the support obtained after coating and drying varies depending on the application, but generally 0.5 to 5.0 g / m ² is preferred for a lithographic printing plate material. As a method of applying, various methods can be used, for example,
Examples include bar coater coating, spin coating, spray coating, curtain coating, dip coating, air knife coating, blade coating, roll coating, and the like. As the coating amount decreases, the apparent sensitivity increases, but the film characteristics of the image recording film deteriorate.

In the lithographic printing plate material of the present invention, a surfactant for improving coating properties, for example, a surfactant described in
A fluorine-based surfactant as described in JP-A-170950 can be added. The preferred amount is
It is 0.01 to 1% by weight, more preferably 0.05 to 0.5% by weight, based on the total solid content of the lithographic printing plate material.

The support used in the present invention is a dimensionally stable plate-like material such as paper, plastic (eg, polyethylene, polypropylene, polystyrene, etc.) laminated paper, metal plate ( For example, aluminum, zinc, copper, etc.), plastic film (for example, cellulose diacetate, cellulose triacetate, cellulose propionate, cellulose butyrate, cellulose acetate butyrate,
Cellulose nitrate, polyethylene terephthalate, polyethylene, polystyrene, polypropylene, polycarbonate, polyvinyl acetal, etc.), and paper or plastic films on which a metal as described above is laminated or vapor-deposited.

As the support of the present invention, a polyester film or an aluminum plate is preferable. Among them, an aluminum plate which has good dimensional stability and is relatively inexpensive is particularly preferable. Suitable aluminum plates are a pure aluminum plate and an alloy plate containing aluminum as a main component and containing a trace amount of a different element, and may be a plastic film on which aluminum is laminated or vapor-deposited. The foreign elements contained in aluminum alloys include silicon, iron, manganese,
Copper, magnesium, chromium, zinc, bismuth, nickel, titanium and the like. The content of the foreign element in the alloy is at most 10% by weight or less. Aluminum which is particularly preferred in the present invention is pure aluminum. However, completely pure aluminum is difficult to produce due to refining technology, and therefore may contain a slightly different element. As described above, the composition of the aluminum plate applied to the present invention is not specified, and an aluminum plate of a conventionally known and used material can be appropriately used. The thickness of the aluminum plate used in the present invention is about 0.1 mm to 0.6 mm, preferably 0.15 mm to 0.4 mm, particularly preferably 0.2 mm to 0.8 mm.

Prior to roughening the aluminum plate, if necessary, a degreasing treatment with, for example, a surfactant, an organic solvent, or an alkaline aqueous solution is performed to remove rolling oil on the surface. The surface roughening treatment of the surface of the aluminum plate is performed by various methods, for example, a method of mechanically roughening the surface, a method of electrochemically dissolving the surface, and a method of selectively dissolving the surface chemically. It is performed by the method of causing. As a mechanical method, a known method such as a ball polishing method, a brush polishing method, a blast polishing method, and a buff polishing method can be used. Further, as an electrochemical surface roughening method, there is a method of performing an alternating or direct current in a hydrochloric acid or nitric acid electrolyte. Further, a method combining both of them can be used as disclosed in JP-A-54-63902. The aluminum plate thus roughened is subjected to an alkali etching treatment and a neutralization treatment, if necessary, and then subjected to an anodic oxidation treatment, if desired, in order to increase the water retention and abrasion resistance of the surface. As the electrolyte used for the anodic oxidation treatment of the aluminum plate, various electrolytes that form a porous oxide film can be used. Generally, sulfuric acid,
Phosphoric acid, oxalic acid, chromic acid or a mixed acid thereof is used. The concentration of these electrolytes is appropriately determined depending on the type of the electrolyte.

Since the anodizing treatment conditions vary depending on the electrolyte used, they cannot be specified unconditionally. Generally, however, the concentration of the electrolyte is 1 to 80% by weight, the solution temperature is 5 to 70 ° C., and the current density is 5 to 60 A. / Dm ² , a voltage of 1 to 100 V, and an electrolysis time of 10 seconds to 5 minutes are appropriate. When the amount of the anodic oxide film is less than 1.0 g / m ² , the printing durability is insufficient or the non-image portion of the lithographic printing plate is easily scratched,
So-called "scratch stains" in which ink adheres to scratches during printing are likely to occur. After the anodizing treatment, the aluminum surface is subjected to a hydrophilic treatment as necessary. U.S. Pat. Nos. 2,7,7
No. 14,066, No. 3,181,461, No. 3,2
There is an alkali metal silicate (e.g., sodium silicate aqueous solution) method as disclosed in U.S. Pat. Nos. 80,734 and 3,902,734. In this method, the support is immersed in an aqueous solution of sodium silicate or electrolytically treated. In addition, potassium fluoride zirconate disclosed in JP-B-36-22063 and U.S. Pat. Nos. 3,276,868 and 4,158,461.
And the method of treating with polyvinyl phosphonic acid as disclosed in JP-A No. 4,689,272.

In the lithographic printing plate material according to the present invention, an undercoat layer can be provided on the support, if necessary. As the undercoat layer component, various organic compounds are used, for example, carboxymethyl cellulose, dextrin, gum arabic, phosphonic acids having an amino group such as 2-aminoethylphosphonic acid, and phenylphosphonic acid optionally having a substituent Organic phosphonic acids such as naphthylphosphonic acid, alkylphosphonic acid, glycerophosphonic acid, methylenediphosphonic acid and ethylenediphosphonic acid, phenylphosphoric acid which may have a substituent, naphthylphosphoric acid, alkylphosphoric acid and glycerophosphoric acid Organic phosphinic acid, optionally substituted phenylphosphinic acid, naphthylphosphinic acid, organic phosphinic acid such as alkylphosphinic acid and glycerophosphinic acid, amino acids such as glycine and β-alanine, and hydrochloric acid of triethanolamine Hydroxy such as salt -Alanine, and hydrochlorides of amines having a group may be used in combination of two or more. The coating amount of the organic undercoat layer is suitably from ² to 200 mg / m ² .

As described above, a lithographic printing plate using the lithographic printing plate material according to the present invention can be produced. This lithographic printing plate material has a wavelength of 760 nm to 120.
Image exposure is performed by a solid-state laser and a semiconductor laser that emit 0-nm infrared light. In the present invention, the developing treatment may be performed immediately after the laser irradiation, but it is preferable to perform the heating treatment between the laser irradiation step and the developing step. The heat treatment is preferably performed in a range of 80 ° C. to 150 ° C. for 10 seconds to 5 minutes. By this heat treatment, the laser energy required for recording at the time of laser irradiation can be reduced.

After performing a heat treatment as required, the lithographic printing plate material according to the present invention is developed with an alkaline aqueous solution. As the developer and replenisher for the lithographic printing plate material according to the present invention, conventionally known alkaline aqueous solutions can be used. For example, sodium silicate, potassium silicate, sodium triphosphate, potassium triphosphate, third
Ammonium phosphate, dibasic sodium phosphate, dibasic potassium phosphate, dibasic ammonium phosphate, sodium carbonate, potassium carbonate, ammonium carbonate, sodium bicarbonate, potassium bicarbonate, ammonium bicarbonate, sodium borate, potassium borate, boric acid Ammonium,
And inorganic alkali salts such as sodium hydroxide, ammonium hydroxide, potassium hydroxide and lithium hydroxide. Also, monomethylamine, dimethylamine, trimethylamine, monoethylamine, diethylamine, triethylamine, monoisopropylamine, diisopropylamine, triisopropylamine, n-butylamine, monoethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, Organic alkali agents such as ethyleneimine, ethylenediamine and pyridine are also used. These alkali agents are used alone or in combination of two or more.

Among these alkaline agents, particularly preferred developers are aqueous solutions of silicates such as sodium silicate and potassium silicate. The reason is that the developability can be adjusted by the ratio and the concentration of the silicon oxide SiO ₂ and the alkali metal oxide M ₂ O which are the components of the silicate. For example, JP-A-54-62004 discloses Tokiko 57-74
An alkali metal silicate described in No. 27 is effectively used.

Further, when developing using an automatic developing machine, an aqueous solution having a higher alkali strength than the developing solution (replenisher)
It has been known that a large amount of lithographic printing plate material can be processed without replacing the developing solution in the developing tank for a long time by adding to the developing solution. This replenishment system is also preferably applied in the present invention. Various surfactants and organic solvents can be added to the developing solution and the replenishing solution as required for the purpose of accelerating or suppressing the developing property, dispersing the developing residue and improving the ink affinity of the printing plate image area. Preferred surfactants include anionic, cationic, nonionic and amphoteric surfactants. Further, if necessary, the developer and replenisher may be hydroquinone, resorcin, sulfurous acid,
A reducing agent such as a sodium salt or a potassium salt of an inorganic acid such as bisulfite, an organic carboxylic acid, an antifoaming agent, and a water softener can also be added. The printing plate developed using the above developer and replenisher is post-treated with washing water, a rinsing solution containing a surfactant and the like, and a desensitizing solution containing gum arabic and a starch derivative. When the lithographic printing plate material according to the present invention is used as a printing plate material, these processes can be used in various combinations as a post-treatment.

In recent years, in the plate making / printing industry, automatic developing machines for printing plate materials have been widely used in order to rationalize and standardize plate making operations. This automatic developing machine generally consists of a developing section and a post-processing section, and consists of a device for transporting printing plate material, each processing solution tank and a spray device, and pumps the exposed printing plate horizontally while pumping it. Each processing liquid is sprayed from a spray nozzle to perform development processing.
Recently, a method has been known in which a printing plate material is immersed and transported by a submerged guide roll or the like in a processing liquid tank filled with a processing liquid, and the processing is performed. In such an automatic processing, the processing can be performed while replenishing each processing liquid with a replenisher according to the processing amount, the operating time, and the like. Further, a so-called disposable processing method in which processing is performed with a substantially unused processing liquid can also be applied.

The lithographic printing plate obtained as described above can be subjected to a printing step after applying a desensitized gum if desired. Is subjected to a burning process. If you plan to burn the lithographic printing plate,
It is preferable to treat with a surface-regulating liquid as described in JP-B-61-2518, JP-B-55-28062, JP-A-62-31859 and JP-A-61-159655. As a method, a sponge or absorbent cotton impregnated with the surface conditioning liquid is applied on a lithographic printing plate, or a method in which the printing plate is immersed in a vat filled with the surface conditioning solution and applied, Application by an automatic coater or the like is applied. Also,
Making the amount of the coating uniform with a squeegee or a squeegee roller after the coating gives more preferable results. The application amount of surface conditioning liquid is generally 0.03 to 0.8 g
/ M ² (dry weight) is appropriate.

The lithographic printing plate to which the surface conditioning liquid has been applied is dried if necessary, and then heated to a high temperature using a burning processor (for example, BP-1300, a burning processor sold by Fuji Photo Film Co., Ltd.). Is done. The heating temperature and time in this case depend on the type of the component forming the image, but may be 1 to 180 ° C. to 300 ° C.
A range of up to 20 minutes is preferred. The burned lithographic printing plate can be subjected to conventional treatments such as washing with water and gumming, if necessary, but a surface conditioning liquid containing a water-soluble polymer compound or the like is used. In such a case, a so-called desensitizing treatment such as gumming can be omitted. The lithographic printing plate obtained by such a process is set on an offset printing machine or the like and used for printing a large number of sheets.

In the case of preparing a lithographic printing plate requiring no dampening solution in the present invention, after exposure, heating is performed to promote an insolubilization reaction by an acid generated from an acid precursor. This heating step is performed at a temperature of 80 to 150 ° C. for 5 seconds to 20 seconds.
Minutes.

The photosensitive lithographic printing plate requiring no dampening solution after exposure and, if necessary, a heating step is a developer capable of dissolving or swelling part or all of the photosensitive layer in the image area, or swelling the silicone rubber layer. It is developed with the resulting developer. In this case, there are cases where the photosensitive layer in the image area and the silicone rubber layer thereon are removed, and cases where only the silicone rubber layer in the image area is removed, which can be controlled by the strength of the developer. .

As a developer used for developing a lithographic printing plate using the lithographic printing plate material of the present invention, those known as developing solutions for photosensitive printing plates requiring no dampening solution can be used. For example, aliphatic hydrocarbons (hexane, heptane, "Isoper E, H, G" (trade names of aliphatic hydrocarbons manufactured by Esso Chemical Co., Ltd.) or gasoline, kerosene, etc.), aromatic hydrocarbons (toluene , Xylene, etc.), or a halogenated hydrocarbon (trichlene, etc.) to which the following polar solvent is added, or the polar solvent itself is preferable.・ Alcohols (methanol, ethanol, propanol, benzyl alcohol, ethylene glycol monophenyl ether, 2-methoxyethanol, 2-ethoxyethanol, carbitol monomethyl ether, carbitol monoethyl ether, triethylene glycol monoethyl ether, propylene glycol monomethyl Ether, propylene glycol monoethyl ether, dipropylene glycol monomethyl ether, polyethylene glycol monomethyl ether, propylene glycol, polypropylene glycol, triethylene glycol, tetraethylene glycol) Ketones (acetone, methyl ethyl ketone) Esters (ethyl acetate, methyl lactate) , Ethyl lactate,
Butyl lactate, propylene glycol monomethyl ether acetate, carbitol acetate, dimethyl phthalate, diethyl phthalate) Others (triethyl phosphate, tricresyl phosphate)

Further, water may be added to the organic solvent-based developer, or the solvent may be solubilized in water using a surfactant, or an alkali agent such as sodium silicate, potassium silicate, water Sodium oxide, potassium hydroxide, lithium hydroxide, tribasic sodium phosphate, dibasic sodium phosphate, tribasic ammonium phosphate, dibasic ammonium phosphate, sodium metasilicate, sodium bicarbonate,
An inorganic alkali agent such as ammonia water or an organic alkali agent such as tetraalkylammonium hydride, monoethanolamine, diethanolamine, triethanolamine and the like can be added.

In some cases, tap water or alkaline water can be used simply as a developing solution, and a surfactant or an organic solvent as described above can be added as necessary. Further, it is also possible to add a dye such as crystal violet or Astrazone Red to the developing solution and simultaneously perform the dyeing. The development can be performed by a known method, for example, by rubbing the plate surface with a developing pad containing the above-described developer, or rubbing the developer with the developer brush after pouring the developer onto the plate surface. The developer can be developed at any temperature, but is preferably from 10 to 50 ° C.

The printing plate thus obtained can be detected by dyeing the exposed image portion with a dyeing solution in order to confirm the image forming property. When the developing solution does not contain a dye for dyeing the exposed image portion, it is dyed with the dyeing solution after development. By impregnating the dyeing solution into a soft pad and rubbing the image area lightly, only the image area is stained, whereby it can be confirmed that the development is sufficiently performed up to the highlight area. As the dyeing solution, one or more selected from water-soluble disperse dyes, acid dyes and basic dyes are dissolved in water, alcohols, ketones, ethers or the like alone or in a mixture of two or more. Alternatively, those dispersed are used. Carboxylic acids to improve dyeability,
It is also effective to add amines, surfactants, dyeing assistants, defoamers and the like.

The printing plate dyed with the dyeing solution is preferably washed with water and then dried, whereby the stickiness of the printing plate surface can be suppressed and the handleability of the printing plate can be improved. When printing plates thus processed are stacked and stored, it is preferable to insert and insert a slip sheet to protect the plate surface.

The above-described development and dyeing, or subsequent washing and drying, are preferably carried out by an automatic processor. A preferable example of such an automatic processor is described in JP-A-2-22661.

When the present invention is applied to a so-called non-process type printing plate, the plate may be mounted on a printing machine immediately after laser drawing, and printing may be performed. However, it is preferable to perform heat treatment after laser irradiation. The heat treatment is preferably performed at a temperature of 80 to 150 ° C. for 10 seconds to 5 minutes. By this heat treatment, the laser energy required for recording at the time of laser irradiation can be reduced.

[0111]

The present invention will be described below in detail with reference to examples.
However, the present invention is not limited to these.Example 1 0.30mm thick aluminum plate (material 1050)
After washing with trichlorethylene and degreasing,
And a 400 mesh pumicestone-water suspension.
Was grained and washed well with water. 45
Dipped in a 25% aqueous solution of sodium hydroxide for 9 seconds.
After washing with water, further 2% HNO _Three20 seconds
It was immersed in water for washing. Etching on the grained surface at this time
Approximately 3 g / m^TwoMet. Next, this plate is_TwoS
O_FourCurrent density 15A / dm^Two3g / m
^Two, And then washed with water and dried. next
The following undercoating liquid is applied to this aluminum plate,
Dry for 30 seconds. The amount of coating after drying is 10 mg / m^TwoIn
Was.

(Undercoating solution) 0.1 g of β-alanine 0.05 g of phenylphosphonic acid 40 g of methanol 60 g of pure water Further, a triethylamine salt of p-toluenesulfonic acid was added to this aluminum plate to adjust the pH to 5.0. The following photosensitive solution adjusted to 0 was applied and dried at 100 ° C. for 2 minutes to obtain a negative photosensitive lithographic printing plate. The weight after drying was 2.0 g / m ² .

(Photosensitive solution) ・ Infrared absorber (Compound-1) 0.1 g ・ 4- (pN, N-bis (ethoxycarbonylmethyl) aminophenyl) -2,6-bis (trichloromethyl)- s-Triazine 0.1 g Novolak resin obtained from cresol and formaldehyde (meta: para ratio = 8: 2, weight average molecular weight 5800) 1.2 g Resol resin obtained from bisphenol A and formaldehyde (weight average molecular weight 1600) 1.0 g ・ Dye in which the counter ion of Victoria Pure Blue BOH is converted to 1-naphthalene-sulfonic acid 0.05 g ・ MegaFac F-177 (manufactured by Dainippon Ink and Chemicals, Ltd., fluorine-based surfactant) 0 0.06 g ・ Methyl ethyl ketone 20 g ・ Methyl alcohol 7 g

The obtained negative type lithographic printing plate was treated with a semiconductor laser (wavelength: 825 nm,
Beam diameter: 1 / e ² = 6 μm) and a linear velocity of 8 m / s
The plate output was adjusted to 110 mW by ec, and exposure was performed. After a heat treatment at 110 ° C. for 1 minute after the exposure, a developing solution manufactured by Fuji Photo Film Co., Ltd., DP-4 (1: 8), a rinsing solution FR-
3 (1: 7) through an automatic processor.
Next, gum GU-7 (1: 1) manufactured by Fuji Photo Film Co., Ltd.
The plate was processed in 1) and printed with a Heidel KOR-D machine. 60,000 good prints without stains on the non-image area were obtained.

Example 2 A negative lithographic printing plate was obtained in the same manner as in Example 1 except that Compound 2 or Compound 9 was used as the infrared absorbing agent. After exposing the obtained plate material with a YAG laser adjusted to a plate surface output of 2 W, a developing solution manufactured by Fuji Photo Film Co., Ltd., DP-4 (1: 8), and a rinsing solution FR-3 (1: 7) were used. Processing was carried out through the automatic processor charged. Next, gum GU- manufactured by Fuji Photo Film Co., Ltd.
The plate was processed at 7 (1: 1) and printed on a Heidel KOR-D machine. In each case, 70,000 good prints with no stain on the non-image area were obtained.

Comparative Example 1 In Example 1, a dispersion of carbon black was used as an infrared absorbent. The coating solution was uniform immediately after mixing, but agglomeration occurred over 3 days, and a uniform coating could not be obtained.

Example 3 (Synthesis of Crosslinking Agent) 20 g of 1- [α-methyl-α- (4-hydroxyphenyl) ethyl] -4- [α, α-bis (4-hydroxyphenyl) ethyl] benzene was added to water It was dissolved in 100 ml of an aqueous solution of potassium oxide (10%). 60 ml of formalin (37%) was added dropwise to this reaction solution over 1 hour while stirring at room temperature. After the reaction solution was further stirred at room temperature for 6 hours, it was poured into an aqueous sulfuric acid solution to cause crystallization. The obtained paste-like precipitate was thoroughly washed with water, and then recrystallized from 30 ml of methanol to obtain a white powder. Yield 20 g. The obtained compound is a hexamethylolated product of 1- [α-methyl-α- (4-hydroxyphenyl) ethyl] -4- [α, α-bis (4-hydroxyphenyl) ethyl] benzene by NMR. I understood. Reversed phase HPLC (column: Shimpac CLC
-ODS (manufactured by Shimadzu Corporation), solvent: methanol / water = 6
(0/40 → 90/10), the purity of the hexamethylolated product was 92%.

20 g of this hexamethylol compound was dissolved by heating in 1000 ml of methanol, 1 ml of concentrated sulfuric acid was added, and the mixture was heated under reflux for 12 hours. After cooling the reaction solution, 2 g of potassium carbonate was added, and the mixture was further stirred and concentrated, and ethyl acetate was added.
After adding 0 ml, washing with water and drying, the solvent was distilled off to obtain a white solid. Yield 22 g. The obtained compound is a hexamethoxymethylated product of 1- [α-methyl-α- (4-hydroxyphenyl) ethyl] -4- [α, α-bis (4-hydroxyphenyl) ethyl] benzene by NMR. I understand. Reversed phase HPLC (column: Shimpac C
The purity of hexamethoxymethylated product by LC-ODS (manufactured by Shimadzu Corporation), solvent: methanol / water = 60/40 → 90/10) was 90%.

The same processing as in Example 1 was carried out, and the following photosensitive liquids were added to an undercoated aluminum plate, and the pH was adjusted to 3.0, 4.0 and 5.0 by adding triethylamine salt of p-toluenesulfonic acid. It was applied and dried at 100 ° C. for 2 minutes to obtain negative photosensitive lithographic printing plates A, B and C. The weight after drying was 2.0 g / m ² .

(Photosensitive solution) ・ Infrared absorbing agent (compound-2) 0.1 g ・ The crosslinking agent 0.21 g ・ Phenol-formaldehyde novolak (weight average molecular weight 12000) 2.1 g ・ Diphenyliodonium-9,10- 0.02 g of dimethoxyanthracene sulfonate-Megafac F-176 (fluorinated surfactant manufactured by Dainippon Ink and Chemicals, Inc.) 0.06 g-15 g of methyl ethyl ketone-12 g of 2-methoxy-1-propanol The resulting negative type lithographic printing plate was processed and printed under the same conditions as in Example 1, and a good printed matter having no stain on the non-image area was obtained. The number of prints obtained at this time was 60,000. Next, the printing plate was stored at 45 ° C. and a relative humidity of 75%, and subjected to the same processing. Similarly, a good printed matter having no stain on the non-image area was obtained.

Comparative Example 2 In Example 3, a negative type lithographic printing plate was prepared by using NK3555 manufactured by Nippon Kosaku Dye as an infrared absorbing agent. This printing plate could be processed well immediately after production, but when stored under the same conditions as in Example 3, the image forming ability was lost.

Example 4 The following photosensitive solution was applied to the surface-treated Al plate used in Example 1 to prepare a positive type lithographic printing plate. (Photosensitive solution) ・ Infrared absorber (Compound-2) 0.10 g ・ Esterified product of naphthoquinone-1,2-diazide-sulfonyl chloride and pyrogallol-acetone resin (U.S. Pat. No. 3,635,709) Novolak resin obtained from cresol and formaldehyde (meta: para ratio = 6: 4, weight average molecular weight 1800) 2.00 g p-octylphenol-formaldehyde novolak 0.02 g Naphthoquinone-1,2-diazido-4-sulfonyl chloride 0.01 g tetrahydrophthalic anhydride 0.05 g 4- (p-N, N-bis (ethoxycarbonylmethyl) aminophenyl) -2,6-bis (trichloro Methyl) -s-triazine 0.02 g ・ 4- (pN- (p-H Roxybenzoyl) aminophenyl) -2,6-bis (trichloromethyl) -s-triazine 0.02 g ・ Dye in which the counter ion of Victoria Pure Blue BOH is converted to 1-naphthalene-sulfonic acid 0.03 g ・ MegaFac F- 177 (manufactured by Dainippon Ink and Chemicals, Inc., fluorine-based surfactant) 0.06 g-methyl ethyl ketone 20 g-methyl alcohol 7 g

The obtained positive type lithographic printing plate material was exposed with a YAG laser adjusted to a plate surface output of 2 W, and then developed by Fuji Photo Film Co., Ltd., DP-4 (1: 8), rinse solution FR -3 (1: 7) through an automatic processor. Next, Gum GU-7 manufactured by Fuji Photo Film Co., Ltd.
The plate was processed at (1: 1) and printed with a Heidel KOR-D machine. 70,000 good prints with no stain on the non-image area were obtained.

Example 5 [Preparation of unprocessed lithographic printing plate] (Synthesis of sulfonic acid-generating polymer compound) <Synthesis of monomer> 200 ml of acetonitrile, 11 g of cyclohexyl alcohol and 8.8 g of pyridine were mixed in 50 parts.
The mixture was placed in a 0 ml three-necked flask and stirred. While cooling with ice, 20.2 g of vinylbenzenesulfonyl chloride was added dropwise. After the dropwise addition, the mixture was stirred at room temperature for 2 hours, poured into 1 liter of water, and extracted with ethyl acetate. After drying over magnesium sulfate, the solvent was distilled off under reduced pressure, and the residue was purified by column chromatography using silica gel to obtain a monomer (cyclohexyl ester of p-vinylbenzenesulfonic acid). The calculated value of the elemental analysis is C:
63.13%, H: 6.81%, measured value: C: 6
3.01%, H: 6.85%.

<Synthesis of Sulfonic Acid Generating Polymer Compound>
20 g of the monomer synthesized above and 40 g of methyl ethyl ketone were placed in a 200 ml three-necked flask,
Under a nitrogen stream, azobisdimethylvaleronitrile 0.25
g was added. After stirring at the same temperature for 5 hours, the solvent was distilled off under reduced pressure to obtain a solid. According to GPC (polystyrene standard), it was found to be a polymer having a weight average molecular weight of 104,000.

(Preparation of Unprocessed Lithographic Printing Plate) Thickness 0.3
Trichloride 0mm aluminum plate (material 1050)
After washing with ethylene and degreased, use a nylon brush and 400
Sand the surface with a mesh pumicestone-water suspension.
It was sharpened and washed well with water. 25% of this plate at 45 ° C
Immerse in sodium hydroxide aqueous solution for 9 seconds to etch
After washing with water, 2% HNO _ThreeSoak for 20 seconds
Washed with water. At this time, the etching amount of the grained surface is about 3
g / m^TwoMet. Next, this plate is_TwoSO_FourThe electrolysis
Current density 15A / dm as liquid^Two3g / m^TwoDC positive
After providing an extremely oxidized film, it was washed and dried. Next, add the following solution
Prepared and applied to the above treated aluminum plate,
It was dried at 00 ° C. for 2 minutes to obtain a lithographic printing plate precursor. Dry
After weight 1.2g / m^TwoMet.

(Solution) 1.00 g of sulfonic acid-generating polymer compound synthesized above. 0.15 g of infrared absorber (Compound-2). The counter ion of Victoria Pure Blue BOH was changed to 1-naphthalene-sulfonic acid. Dye 0.05g-Megafac F-177 (manufactured by Dainippon Ink and Chemicals, Inc., fluorine-based surfactant) 0.06g-Methyl ethyl ketone 20g-Methyl alcohol 7g

The obtained lithographic printing plate precursor was placed at a wavelength of 106
Exposure was performed with a YAG laser emitting infrared light of 4 nm. After exposure, heat treatment was performed at 110 ° C. for 1 minute.
-Printed on D machine. At this time, it was observed whether or not stains occurred on the non-image portion of the printed matter. A good printed matter with no stain on the non-image area was obtained.

Example 6 [Preparation of a positive type lithographic printing plate requiring no fountain solution] (Preparation of support) A 1S aluminum plate having a thickness of 0.24 mm was treated with 10% sodium tertiary phosphate kept at 80 ° C. Degreased by immersion in a 3% aqueous solution for 3 minutes, grained with a nylon brush, etched for about 10 minutes with sodium aluminate, and desmutted with a 3% aqueous solution of sodium hydrogen sulfate. This aluminum plate was anodized in a 20% sulfuric acid at a current density of 2 A / dm ² for 2 minutes.

A coating solution having the following composition was applied on the support so as to have a dry film thickness of 1 μm, and heated (at 100 ° C., 1 ° C.)
Min) and dried to form a primer layer. -Samprene IB1700D (polyurethane manufactured by Sanyo Chemical Co., Ltd.) 10 parts by weight-Hexafluorophosphate of polycondensation product of p-diazodiphenylamine and paraformaldehyde 0.1 part by weight-Defensor MCF323 (Dainippon Ink & Chemicals, Inc.) 0.03 parts by weight-Propylene glycol methyl ether acetate 50 parts by weight-Methyl lactate 20 parts by weight-Pure water 1 part by weight

Thereafter, FT261V UDNS ULTRA-
Exposure was performed for 20 counts using a PLUS FLIPTOP PLATE MAKER vacuum exposure machine.

(Photosensitive Layer) The photosensitive solution used in Example 2 was applied to the aluminum plate and dried at 90 ° C. for 1 minute.
The coating weight after drying was 2 g / m ² .

(Silicone Rubber Layer) The following silicone rubber composition solution was applied on the above-mentioned photosensitive layer to a dry weight of 2 g / m ² and dried at 100 ° C. for 2 minutes.・ Α, ω-divinylpolydimethylsiloxane (degree of polymerization: about 700) 9 parts by weight ・ (CH ₃ ) ₃ -Si-O- (SiH (CH ₃ ) -O) ₈ -Si (CH ₃ ) ₃ 0.5 Parts by weight ・ Polydimethylsiloxane (degree of polymerization: about 8,000) 0.5 part by weight ・ Olefin-chloroplatinic acid 0.08 part by weight ・ Inhibitor (CH≡C-Si (CH ₃ ) ₂ OSi (CH ₃ ) ₃ ) 0.3 parts by weight ・ γ-methacryloxypropyltrimethoxysilane 0.3 parts by weight ・ Isopar-E (manufactured by Esso Chemical Co., Ltd.) 140 parts by weight

An 8 μm-thick biaxially oriented polypropylene film was laminated on the surface of the silicone rubber layer obtained as described above to obtain a photosensitive lithographic printing plate requiring no dampening water. The printing plate obtained was adjusted to a plate surface output of 2 W by YAG.
After exposing with a laser, the laminated film was peeled off and heated in an oven at 100 ° C. for 3 minutes. After the heated printing plate was immersed in a solution of tripropylene glycol at 40 ° C. for 1 minute, the plate surface was rubbed with a developing pad in water.
In the unexposed area, a positive type fountain solution-free lithographic printing plate was obtained in which the photosensitive layer was exposed.

Example 7 A positive type lithographic printing plate was prepared by applying the photosensitive solution in Example 4 with the following changes. (Photosensitive solution) ・ Infrared absorber (compound-2) 0.10 g ・ Novolak resin obtained from cresol and formaldehyde (meta: para ratio = 6: 4, weight average molecular weight 1800) 2.00 g ・ Victoria pure blue BOH Dye with ions converted to 1-naphthalene-sulfonic acid 0.03 g Megafac F-177 (a fluorinated surfactant manufactured by Dainippon Ink and Chemicals, Inc.) 0.06 g Methyl ethyl ketone 20 g Methyl alcohol 7 g

The obtained lithographic printing plate material was subjected to a plate output of 2 W
After exposure with a YAG laser adjusted to the following conditions, a developing solution manufactured by Fuji Photo Film Co., Ltd., DP-4 (1: 8), a rinsing solution FR
-3 (1: 7) through an automatic processor. A clear positive image was obtained. Subsequently, the plate surface was treated with gum GU-7 (1: 1) manufactured by Fuji Photo Film Co., Ltd., and printing was performed with a Heidel KOR-D machine. A good printed matter with no stain on the non-image area was obtained.

Example 8 The following solution was applied to the surface-treated and undercoated aluminum support obtained in Example 1 and dried by heating at 100 ° C. for 1 minute to prepare a negative type lithographic printing plate. Wood was obtained. The coating weight after drying was 1.5 g / m ² .

(Photosensitive solution) ・ Infrared absorber (compound 26) 0.07 g ・ Acid generator (SH-1 below) 0.3 g ・ 2,4-bishydroxymethyl-6-methylphenol 0.5 g -Marka Linker MS S-4P (Poly (p-hydroxystyrene) 1.5 g from Maruzen Petrochemical Co., Ltd.)-AIZEN SPIRON BLUE C-RH (Hodogaya Chemical Co., Ltd.) 0.035 g-Mega FAK F-177 (manufactured by Dainippon Ink and Chemicals, Inc., fluorine-based surfactant) 0.01 g-methyl ethyl ketone 12 g-methyl alcohol 10 g-1-methoxy-2-propanol 8 g

[0139]

Embedded image

Under the same conditions as in Example 1, laser exposure, heating, and development were performed, and then printing was performed. As a result, as in the case of Example 1, 60,000 good printed matters without stains on the non-image area were obtained.

[0141]

According to the present invention, by using a specific infrared absorbing material, plate making can be performed directly from digital data of a computer or the like, and furthermore, the stability during storage is excellent, and a dispersion step is performed in the production of a printing plate coating solution. It is possible to provide a laser direct-writing type lithographic printing plate material which can be easily manufactured without uniformity and has a uniform coating.

Claims (5)

[Claims] 1. A laser direct drawing type lithographic printing plate material comprising a dihydroperimidine squarylium compound or a mixture thereof. 2. The dihydroperimidine squarylium
The compound is a compound represented by the following general formula (1).
The laser direct drawing type lithographic printing according to claim 1, characterized in that:
Plate material. General formula (1)Where R¹, R^Two, R^Three, R^Four, R^Five, R⁶, R⁷, R
⁸, R⁹, R^Ten, R¹¹And R¹²Is the hydrogen source
, Alkyl group, cycloalkyl group, aryl group, ara
Alkyl, alkenyl, alkynyl or acyl groups
And R¹And R ^Two, R^ThreeAnd R^Four, R^FiveAnd R⁶, R⁷When
R⁸, R⁹And R^Ten, R¹¹And R¹², R^TwoAnd R ^Three, R⁶And R
⁷, And R^TenAnd R¹¹Of the combinations selected from
One or more of which are bonded to each other to form a 5- or 6-membered ring
A ring may be formed. n represents an integer of 1 to 6. X¹,
X^TwoAnd X^ThreeRepresents a hydrogen atom or a monovalent group,
m represents an integer of 1 to 3. 3. The dihydroperimidine squarylium
The compound is a compound represented by the following general formula (2).
The laser direct drawing type lithographic printing according to claim 1, characterized in that:
Plate material. General formula (2)Where R¹, R^Two, R^Three, R^Four, R^Five, R⁶, R⁷And
And R⁸Represents a hydrogen atom, an alkyl group,
Kill group, aryl group, aralkyl group, alkenyl group,
A alkynyl group or an acyl group;¹And R^Two, R^ThreeWhen
R^Four, R^FiveAnd R ⁶, R⁷And R⁸, R^TwoAnd R^Three,and,
R⁶And R⁷One or more of the combinations selected from
Bond to each other to form a 5- or 6-membered ring
Is also good. X¹And X^TwoEach represents a hydrogen atom or a monovalent group
And m represents an integer of 1 to 3. 4. An alkali-soluble binder, an acid generator,
The composition according to claim 1, further comprising an acid crosslinking compound.
4. The lithographic printing plate material of laser direct-drawing type according to any one of 3. 5. The method according to claim 1, further comprising an alkali-soluble binder, a substance which is thermally decomposable and substantially degrades the solubility of the alkali-soluble binder when not decomposed. A lithographic printing plate material of laser direct-drawing type described in the paragraph.