Novel phenol compounds containing methoxymethyl group or hydroxymethyl group.

FIELD OF THE INVENTION

0001The present invention relates to novel phenol compounds containing a methoxymethyl group or a hydroxymethyl group.

BACKGROUND OF THE INVENTION

0002It has conventionally been known that hydroxymethyl-containing phenol compounds are used in various applications. For example, besides being applied to coating compositions as described in "THE CHEMISTRY OF ORGANIC FILM FORMERS" written by D.H. Solomon, hydroxymethyl-containing phenol compounds are used in many fields such as, e.g., lithographic plates, photoresists, adhesives, molding materials, laminating materials, and binders.

0003Frequently used in these applications are a phenol-formaldehyde-resol resin or the compounds described in Japanese patent publication (examined) No. Hei-1-49932, specifically such compounds as bishydroxymethyl-p-cresol and tetrakis(hydroxymethyl)bisphenol A.

0004However, such conventionally known hydroxymethyl-containing phenol compounds have been disadvantageous in that methylol groups, which function as a crosslinking group, cannot be incorporated in the molecule in a large number. The phenol-formalin-resol resin also is disadvantageous in that the number of the reactive hydroxymethyl groups contained in the molecule is small. Hence, both the hydroxymethyl-containing phenol compounds and the phenol-formaldehyde-resol resin have failed to attain sufficient cured-film performances when used in coating compositions, photosensitive printing plates, etc. It has therefore been necessary that in order to meet cured-film performance requirements, the hydroxymethyl-containing phenol compounds or the resol resin should be incorporated in a large amount.

0005Further, there has been another problem that the incorporation of a hydroxymethyl group results in impaired solvent solubility.

SUMMARY OF THE INVENTION

0006Accordingly, an object of the present invention is to provide a methoxymethyl- or hydroxymethyl-containing phenol compound which has sufficient cured-film performances even when used in a smaller amount as compared with the conventional hydroxymethyl-containing phenol compounds and resol resin.

0007The methoxymethyl- or hydroxymethyl-containing phenol compound of the present invention is represented by the following formula (I), (II), (III), (IV) or (V): <chemistry id="chem0001" num="0001"><img file="EP0632003A1_D0001.tif" /></chemistry><chemistry id="chem0002" num="0002"><img file="EP0632003A1_D0002.tif" /></chemistry><chemistry id="chem0003" num="0003"><img file="EP0632003A1_D0003.tif" /></chemistry> wherein    each R represents CH₂OCH₃, CH₂OH, or H, provided that at least three of the R's are CH₂OCH₃ or CH₂OH, with at least one thereof being CH₂OCH₃;    each R₁ represents CH₂OCH₃, CH₂OH, or H, provided that at least two of the R₁'s are CH₂OH; and    each R₂ represents CH₂OCH₃, CH₂OH, or H, provided that at least two of the R₂'s are CH₂OH.

DETAILED DESCRIPTION OF THE INVENTION

0008In the formula (I), each R represents CH₂OCH₃, CH₂OH, or H, provided that at least three of the R's are CH₂OCH₃ or CH₂OH, with at least one thereof being CH₂OCH₃. The compound is preferably one in which four or more of the R's are CH₂OCH₃ or CH₂OH, more preferably one in which five or more of the R's are CH₂OCH₃ or CH₂OH, and most preferably one in which all the R's are CH₂OCH₃ or CH₂OH, provided that in all cases at least one of these R's is CH₂OCH₃.

0009The methoxymethyl-containing phenol compound of this invention which is represented by formula (I) can be obtained by reacting the following phenol compound represented by formula (I') with formaldehyde in the presence of a basic catalyst and then reacting the reaction product in methanol in the presence of an acid catalyst. <chemistry id="chem0004" num="0004"><img file="EP0632003A1_D0004.tif" /></chemistry>    The phenol compound represented by formula (I'), i.e., 4,4'-[1-[4-[2-(4-hydroxyphenyl)-2-propyl]phenyl]ethylidene]bisphenol, may be a commercially available one. Examples thereof include one commercially available under the name of "TrisP-PA" from Honshu Chemical Industry Co., Ltd. As the formaldehyde for use in this invention, either of formalin and paraformaldehyde is suitable.

0010In the first stage of the synthesis of a phenol compound (I) according to the present invention, the adequate range of the molar ratio of the phenol compound represented by formula (I') to formaldehyde (HCHO) to be introduced into a reactor is from 1:2 to 1:30, and preferably from 1:6 to 1:18 from the standpoint of yield.

0011As the basic catalyst, either of an inorganic base and an organic base is usable. Preferred examples thereof include sodium hydroxide, potassium hydroxide, lithium hydroxide, calcium hydroxide, ammonia (water), tetramethylammonium hydroxide, tetraethylammonium hydroxide, triethylamine, diethylamine, monoethylamine, trimethylamine, dimethylamine, and monomethylamine. The amount of such a basic catalyst to be used is generally from 50 to 300% by mole based on the amount of the phenol compound represented by formula (I'). Since these basic catalysts also function to dissolve the phenol compound represented by formula (I') into water, the amount thereof may be suitably increased or reduced according to the solvent to be used.

0012The reaction temperature is preferably from 0 to 60°C, more preferably from 0 to 45°C. At temperatures less than 0°C, the rate of the condensation reaction is low. At temperatures above 60°C, gelation takes place. The reaction time varies depending on the reaction temperature. For example, in the case of 35°C, a reaction time of 4 to 36 hours is preferred. In this case, if too long a reaction time (e.g., 48 hours or more) is used, gelation may occur.

0013As the acid catalyst to be used in the second stage of the synthesis of the phenol compound of this invention, any of inorganic acids such as sulfuric acid, hydrochloric acid, nitric acid, and phosphoric acid and organic acids such as benzenesulfonic acid, p-toluenesulfonic acid, and acetic acid may be employed.

0014The reaction temperature is preferably from 0 to 65°C, more preferably from 10 to 65°C. At temperatures less than 0°C, the reaction rate is low. The reaction time varies depending on the reaction temperature, concentration, and the amount of the acid catalyst. In the case of 65°C, for example, a reaction time of 0.5 to 36 hours is preferred.

0015In the formulas (II) and (III), each R₁ represents CH₂OCH₃, CH₂OH or H, provided that at least two of the R₁'s are CH₂OH group. The compound is preferably one in which five or more of the R₁'s are CH₂OH, more preferably one in which seven or more of the R₁'s are CH₂OH, and most preferably one in which all the R₁'s are CH₂OH.

0016In the formulas (IV) and (V), each R₂ represents CH₂OCH₃, CH₂OH or H, provided that at least two of the R₂ʼs are CH₂OH group. The compound is preferably one in which three or more of the R₂'s are CH₂OH, more preferably one in which five or more of the R₂'s are CH₂OH, and most preferably one in which all the R₂'s are CH₂OH.

0017The hydroxymethyl-containing phenol compound of this invention which is represented by formula (II), (III), (IV) or (V) can be obtained by reacting the following phenol compound represented by formulas (II'), (III'), (IV') or (V') with formaldehyde in the presence of a basic catalyst: <chemistry id="chem0005" num="0005"><img file="EP0632003A1_D0005.tif" /></chemistry><chemistry id="chem0006" num="0006"><img file="EP0632003A1_D0006.tif" /></chemistry>    The phenol compounds represented by formula (II'), (III') or (IV') can be synthesized by the methods as described in JP-A-55-162728, JP-A-3-179353, JP-A-5-224409 and U.S. Patent 5,296,330 (the term "JP-A" as used herein means an unexamined published Japanese patent application).

0018The phenol compound represented by formula (V') may be a commercially available one under the name of "Trisphenol-Tc" from Mitsui Petrochemical Industries, Ltd.

0019In the synthesis of a hydroxymethyl-containing phenol compound represented by formula (II) or (IV) according to the present invention, the adequate range of the molar ratio of the phenol compound represented by formula (II') or (IV') to formaldehyde (HCHO) to be introduced into a reactor is from 1:2 to 1:40, and preferably from 1:8 to 1:24 from the standpoint of yield. As the formaldehyde for use in this invention, either of formalin and paraformaldehyde is suitable.

0020As the basic catalyst, either of an inorganic base and an organic base is usable. Preferred examples thereof include sodium hydroxide, potassium hydroxide, lithium hydroxide, calcium hydroxide, ammonia (water), tetramethylammonium hydroxide, tetraethylammonium hydroxide, triethylamine, diethylamine, monoethylamine, trimethylamine, dimethylamine, and monomethylamine. The amount of such a basic catalyst to be used is generally from 50 to 600% by mole based on the amount of the phenol compound represented by formula (II') or (IV'). Since these basic catalysts also function to dissolve the phenol compound represented by formula (II') or (IV') into water, the amount thereof may be suitably increased or reduced according to the solvent to be used.

0021The reaction temperature is preferably from 0 to 60°C, more preferably from 10 to 45°C. At temperatures less than 10°C, the rate of the condensation reaction is low. At temperatures above 60°C, gelation takes place. The reaction time varies depending on the reaction temperature. For example, in the case of 40°C, a reaction time of 1 to 36 hours is preferred. In this case, if too long a reaction time (e.g., 48 hours or more) is used, gelation may occur. It is preferred that after completion of the reaction, neutralization with an acid be conducted. As the acid to be used, any of inorganic acids such as sulfuric acid, hydrochloric acid, nitric acid, and phosphoric acid and organic acids such as benzenesulfonic acid, p-toluenesulfonic acid, and acetic acid may be employed.

0022In the synthesis of a hydroxymethyl-containing phenol compound represented by formula (III) according to the present invention, the adequate range of the molar ratio of the phenol compound represented by formula (III') to formaldehyde (HCHO) to be introduced into a reactor is from 1:2 to 1:60, and preferably from 1:12 to 1:36 from the standpoint of yield. The basic catalyst to be used may be the same as that described above, but the amount thereof is preferably from 50 to 1,000% by mole based on the amount of the phenol compound represented by formula (III'). The reaction temperature and reaction time may be the same as those for the phenol compound represented by formula (II) or (IV) described above.

0023In the synthesis of a hydroxymethyl-containing phenol compound represented by formula (V) according to the present invention, the adequate range of the molar ratio of the phenol compound represented by formula (V') to formaldehyde (HCHO) to be introduced into a reactor is from 1:2 to 1:30, and preferably from 1:6 to 1:18 from the standpoint of yield. The basic catalyst to be used may be the same as that described above, but the amount thereof is preferably from 50 to 500% by mole based on the amount of the phenol compound represented by formula (V'). The reaction temperature and reaction time may be the same as those for the phenol compound represented by formula (II) or (IV) described above.

0024Specific examples of the methoxymethyl- or hydroxymethyl-containing phenol compounds of the present invention are shown below, but the present invention is not to be construed as being limited thereto. <chemistry id="chem0007" num="0007"><img file="EP0632003A1_D0007.tif" /></chemistry><chemistry id="chem0008" num="0008"><img file="EP0632003A1_D0008.tif" /></chemistry><chemistry id="chem0009" num="0009"><img file="EP0632003A1_D0009.tif" /></chemistry><chemistry id="chem0010" num="0010"><img file="EP0632003A1_D0010.tif" /></chemistry><chemistry id="chem0011" num="0011"><img file="EP0632003A1_D0011.tif" /></chemistry><chemistry id="chem0012" num="0012"><img file="EP0632003A1_D0012.tif" /></chemistry>    Synthesis Examples for obtaining methoxymethyl- or hydroxymethyl-containing phenol compounds (I), (II), (III), (IV) and (V) of the present invention are given below.

SYNTHESIS EXAMPLE 1

(Synthesis of Compound I-1)

0025Into 100 ml of aqueous potassium hydroxide solution (10%) was dissolved 20 g of the phenol compound represented by formula (I'). To this solution was dropwise added 60 ml of formalin (37%) with stirring at room temperature over a period of 1 hour. After the reaction mixture was stirred at room temperature for further 6 hours, it was poured into an aqueous solution of sulfuric acid to conduct crystallization. The pasty precipitate obtained was sufficiently washed with water and then re-crystallized with 30 ml of methanol to obtain an intermediate of the desired compound as a white powder. The amount of the thus obtained powder was 20 g.    ¹H-NMR (DMSO-d₆) δ: 1.58 (s, 6H), 2.00 (s, 3H), 4.42-5.52 (m, 12H), 5.16-5.24 (m, H), 6.83-7.08 (m, 10H), 8.38 (s, 2H), 8.42 (s, 2H)    The purity was measured by reversed-phase HPLC (column, Shimpac CLC-ODS (manufactured by Shimadzu Corp.); solvent, methanol/water = 60/40 → 90/10), and the content of the hexahydroxymethyl compound was found to be 92%.

0026Into 1,000 ml of methanol was then dissolved 20 g of the hexahydroxymethyl compound with heating. Thereto was added 1 ml of concentrated sulfuric acid. The reaction mixture was heated with refluxing for 12 hours. After the reaction mixture was cooled, 2 g of potassium carbonate was added and the resulting mixture was stirred and then concentrated. Thereto was added 300 ml of ethyl acetate. This mixture was washed with water and dried, and the solvent was then removed to obtain the desired compound as a colorless oily substance. The yield was 22 g.    ¹H-NMR (CDCl₃) δ: 1.62 (s, 6H), 2.07 (s, 3H), 3.38 (s, 18H), 4.49 (s, 18H), 4.49 (s, 8H), 4.55 (s, 4H), 6.80 (s, 4H), 6.90 (d, 2H), 6.98 (s, 2H), 7.06 (d, 2H), 7.64 (s, 1H), 7.70 (s, 2H)    The purity was measured by reversed-phase HPLC (column, Shimpac CLC-ODS (manufactured by Shimadzu Corp.); solvent, methanol/water = 60/40 → 90/10), and the content of the hexamethoxymethyl compound was found to be 90%.

SYNTHESIS EXAMPLE 2

(Synthesis of Compound II-1)

0027Into 25 ml of aqueous sodium hydroxide solution (15%) was dissolved 10 g of the phenol compound represented by formula (II'). To this solution was added 15 ml of methanol. Thereto was then dropwise added 20 g of formalin (37%) with stirring at room temperature. After completion of the dropwise addition, the reaction mixture was heated to 40°C and stirred for further 12 hours. The resulting reaction mixture was poured into an aqueous solution of acetic acid to conduct crystallization. The solid obtained was sufficiently washed with water and then re-slurried with 100 ml of ethyl acetate to obtain 11.4 g of the desired compound as a white powder.    ¹H-NMR (DMSO-d₆) δ: 4.48 (s, 16H), 5.17 (br, 8H), 5.31 (s, 2H), 6.91 (s, 8H), 7.00 (s, 4H), 8.40 (br, 4H)    The purity was measured by reversed-phase HPLC (column, Shimpac CLC-ODS (Shimadzu Corp.); solvent, methanol/water = 60/40 → 90/10), and the content of the octakishydroxymethyl compound (the compound represented by formula (II) wherein all the R₁'s are CH₂OH, i.e., Compound II-1) was found to be 95%.

SYNTHESIS EXAMPLE 3

(Synthesis of Compound III-1)

0028Into a solution obtained by mixing 35 ml of aqueous sodium hydroxide solution (15%) with 25 ml of methanol was dissolved 15 g of the phenol compound represented by formula (III'). To this solution was dropwise added 33 g of formalin (37%) with stirring at room temperature. After completion of the dropwise addition, the reaction mixture was heated to 40°C and stirred for further 20 hours. The resulting reaction mixture was poured into an aqueous solution of acetic acid. A viscous oily substance was separated from the aqueous layer by decantation, sufficiently washed with water, and then dried in a vacuum to thereby obtain 16.6 g of the desired compound as a light-yellow powder.    ¹H-NMR (DMSO-d₆) δ: 1.80 (s, 9H), 4.42 (br, 24H), 6.62 (s, 3H), 6.72 (s, 12H)    The purity was measured by reversed-phase HPLC (column, Shimpac CLC-ODS (Shimadzu Corp.); solvent, methanol/water = 60/40 → 90/10), and the content of the dodecakishydroxymethyl compound (the compound represented by formula (III) wherein all the R₁'s are CH₂OH, i.e., Compound III-1) was found to be 80%.

SYNTHESIS EXAMPLE 4

(Synthesis of Compound IV-1)

0029Into 40 g of aqueous sodium hydroxide solution (10%) was dissolved 11 g of the phenol compound represented by formula (IV'). To this solution was added 10 g of methanol. Thereto was then dropwise added 20 g of formalin (37%) at room temperature. After completion of the dropwise addition, the reaction mixture was heated to 40°C and allowed to react for further 12 hours. The resulting reaction mixture was subjected to crystallization from an aqueous solution of acetic acid to obtain a white viscous solid. This white solid was sufficiently washed with water and then dried in a vacuum at room temperature. The yield was 13.6 g.    ¹H-NMR (DMSO-d₆) δ: 2.11 (br, 8H), 4.47 (s, 8H), 4.48 (s, 8H), 5.19 (br, 8H), 6.84 (s, 4H), 7.00 (s, 4H), 8.40 (br, 4H)    The purity was measured by HPLC (column used, Shimpac CLC-ODS manufactured by Shimadzu Corp.), and the content of the compound represented by formula (IV) in which all the R₂'s are CH₂OH (Compound IV-1) was found to be 93%.

SYNTHESIS EXAMPLE 5

(Synthesis of Compound V-1)

0030Into 60 g of aqueous sodium hydroxide solution (10%) was dissolved 17.25 g of the phenol compound represented by formula (V') (as the phenol compound, use was made of one commercially available under the trade name of "TrisPhenol-Tc" from Mitsui Petrochemical Industries, Ltd). To this solution was added 15 g of methanol. Thereto was then dropwise added 30 g of formalin (37%) at room temperature. After completion of the dropwise addition, the reaction mixture was heated to 40°C and allowed to react for further 12 hours. The resulting reaction mixture was subjected to crystallization from an aqueous solution of acetic acid to obtain a white solid. This white solid was sufficiently washed with water and then dried in a vacuum at room temperature. The yield was 19.9 g.    ¹H-NMR (DMSO-d₆) δ: 1.48 (s, 18H), 4.47 (s, 12H), 5.17 (br, 6H), 6.92 (m, 9H), 8.35 (br, 3H)    The purity was measured by HPLC (column used, Shimpac CLC-ODS manufactured by Shimadzu Corp.), and the content of the compound represented by formula (V) in which all the R₂'s are CH₂OH (Compound V-1) was found to be 90%.

0031The thus-obtained methoxymethyl- or hydroxymethyl-containing phenol compounds represented by formulas (I) to (V) have sufficient cured-film performances even when used in a smaller amount as compared with conventional hydroxymethyl-containing phenol compounds, and are advantageously used as a major ingredient for coating compositions, an additive for molding materials, adhesives, binders, or photosensitive printing plates, etc.

0032Further, the thus-obtained methoxymethyl-containing phenol compound represented by formula (I) is superior in solvent solubility to the compound represented by formula (I) wherein all the R's are CH₂OH group.

0033Application Examples are given below.

APPLICATION EXAMPLE 1 (Lithographic Plate)

0034An aluminum plate (material, 1050) having a thickness of 0.3 mm was degreased by cleaning with trichloroethylene, and the surface of the resulting plate was grained with a nylon brush and an aqueous suspension of a 400-mesh pumice and then sufficiently washed with water. This plate was etched by immersing it in a 45°C 25% aqueous sodium hydroxide solution for 9 seconds and then washed with water. Subsequently, the plate was further immersed in 20% nitric acid for 20 seconds and then washed with water. The aluminum amount thus removed from the grained surface by etching was about 3 g/m². The resulting plate was subjected to direct-current anodizing at a current density of 15 A/dm² using 7% sulfuric acid as the electrolytic solution to deposit an oxide film on the plate in an amount of 3 g/m², and was then washed with water and dried. This aluminum plate was subsequently coated with the primer specified below and dried at 80°C for 30 seconds. The amount of the primer coat after drying was 10 mg/m². <tables id="tabl0001" num="0001"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row><entry namest="col1" nameend="col2" align="left">(Primer)</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">β-Alanine</entry><entry namest="col2" nameend="col2" align="left">0.1 g</entry></row><row><entry namest="col1" nameend="col1" align="left">Phenylphosphonic acid</entry><entry namest="col2" nameend="col2" align="left">0.05 g</entry></row><row><entry namest="col1" nameend="col1" align="left">Methanol</entry><entry namest="col2" nameend="col2" align="left">40 g</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Pure water</entry><entry namest="col2" nameend="col2" align="left">60 g</entry></row></tbody></tgroup></table></tables>

0035Further, the photosensitive solutions specified below were applied on the resulting aluminum plate and the coatings were dried at 100°C for 2 minutes to obtain positive photosensitive lithographic plates. The amount of the coating after drying was 1.8 g/m² for all the photosensitive solutions. <tables id="tabl0002" num="0002"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row><entry namest="col1" nameend="col2" align="left">Photosensitive Solution (unit; gram)</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Product of esterification of naphthoquinone-1,2-diazide-5-sulfonic acid chloride with a pyrogallol-acetone resin</entry><entry namest="col2" nameend="col2" align="right">0.90</entry></row><row><entry namest="col1" nameend="col1" align="left">Cresol-formaldehyde novolak (meta:para ratio = 6:4; weight-average molecular weight, 1,800; unreacted cresol content, 0.5%)</entry><entry namest="col2" nameend="col2" align="right">(as shown in Table 1)</entry></row><row><entry namest="col1" nameend="col1" align="left">p-Octylphenol-formaldehyde novolak</entry><entry namest="col2" nameend="col2" align="right">0.02</entry></row><row><entry namest="col1" nameend="col1" align="left">Naphthoquinone-1,2-diazide-5-sulfonic acid chloride</entry><entry namest="col2" nameend="col2" align="right">0.01</entry></row><row><entry namest="col1" nameend="col1" align="left">Phenol derivative</entry><entry namest="col2" nameend="col2" align="right">(as shown in Table 1)</entry></row><row><entry namest="col1" nameend="col1" align="left">Tetrahydrophthalic anhydride</entry><entry namest="col2" nameend="col2" align="right">0.05</entry></row><row><entry namest="col1" nameend="col1" align="left">4-(p-N,N-diethoxycarbonylaminophenyl)-2,6-bis(trichloromethyl)-s-triazine</entry><entry namest="col2" nameend="col2" align="right">0.02</entry></row><row><entry namest="col1" nameend="col1" align="left">4-(p-N-(p-Hydroxybenzoyl)aminophenyl)-2,6-bis(trichloromethyl)-s-triazine</entry><entry namest="col2" nameend="col2" align="right">0.02</entry></row><row><entry namest="col1" nameend="col1" align="left">Dye obtained from Victoria Pure Blue BOH by converting the counter ion into 1-naphthalenesulfonic acid</entry><entry namest="col2" nameend="col2" align="right">0.03</entry></row><row><entry namest="col1" nameend="col1" align="left">MEGAFAC F-177 (fluorine compound surfactant manufactured by Dainippon Ink and Chemicals Inc.)</entry><entry namest="col2" nameend="col2" align="right">0.15</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Methyl ethyl ketone</entry><entry namest="col2" nameend="col2" align="right">26</entry></row></tbody></tgroup></table></tables><tables id="tabl0003" num="0003"><table frame="all"><title>Table 1</title><tgroup cols="4" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="39.37mm" /><colspec colnum="2" colname="col2" colwidth="39.37mm" /><colspec colnum="3" colname="col3" colwidth="39.37mm" /><colspec colnum="4" colname="col4" colwidth="39.37mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="center">Lithographic plate</entry><entry namest="col2" nameend="col2" align="center">Amount of cresol-formaldehyde novolak used (g)</entry><entry namest="col3" nameend="col4" align="center">Phenol derivative</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" align="center">Formula</entry><entry namest="col4" nameend="col4" align="center">Amount used (g)</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">[A]</entry><entry namest="col2" nameend="col2" align="char" char=".">2.10</entry><entry namest="col3" nameend="col3" align="center">methoxymethylphenol compound (I-1)</entry><entry namest="col4" nameend="col4" align="right">0.06</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">[B]</entry><entry namest="col2" nameend="col2" align="char" char=".">2.16</entry><entry namest="col3" nameend="col3" align="center">none</entry><entry namest="col4" nameend="col4" align="right">-</entry></row></tbody></tgroup></table></tables>

0036These positive photosensitive lithographic plates were exposed to the light from a 30-ampere carbon arc lamp placed at a distance of 70 cm therefrom, and were then subjected to automatic development (by means of "800U," an automatic developing machine manufactured by Fuji Photo Film Co., Ltd.) at 25°C for 40 seconds with DP-4 (trade name; manufactured by Fuji Photo Film Co., Ltd.) diluted 8 times. The proper exposure time for this treatment was the period in which the part corresponding to step 5 on a gray scale having a density difference of 0.15 (manufactured by Fuji Photo Film Co., Ltd.) became completely clear, and this exposure time was taken as the sensitivity of the photosensitive lithographic plate. Further, the time required for the part corresponding to the solid step on the gray scale to undergo a two-step color change therefrom in 40-second tray development with 25°C DP-4 diluted 8 times was determined (this time being hereinafter referred to as "development acceptability").

0037The results of the sensitivity (exposure time) and development acceptability evaluations of these positive photosensitive lithographic plates are shown in Table 2.

0038These photosensitive lithographic plates were then placed on a transparent base and exposed for 60 seconds in a vacuum frame through a positive original film using a halide lamp as a light source. The resulting plates were subsequently processed by passing these through an automatic developing machine containing developing solution DP-4 (1:8) and rinsing solution FR-3 (1:7) manufactured by Fuji Photo Film Co., Ltd. Thereafter, the plate surfaces were wiped with burning conditioner BC-3 manufactured by Fuji Photo Film Co., Ltd., and processed for 7 minutes with burning device BP-1300. The plate surfaces were subsequently treated with a liquid prepared by diluting gum GU-7 manufactured by Fuji Photo Film Co., Ltd. with water 2 times, allowed to stand for 1 day, and then subjected to printing with printing machine Heidel KOR-D. The burning temperature, the number of prints obtained, and the degree of spreading in a halftone image area are shown in Table 2. <tables id="tabl0004" num="0004"><table frame="all"><title>Table 2</title><tgroup cols="7" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="22.50mm" /><colspec colnum="2" colname="col2" colwidth="22.50mm" /><colspec colnum="3" colname="col3" colwidth="22.50mm" /><colspec colnum="4" colname="col4" colwidth="22.50mm" /><colspec colnum="5" colname="col5" colwidth="22.50mm" /><colspec colnum="6" colname="col6" colwidth="22.50mm" /><colspec colnum="7" colname="col7" colwidth="22.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="center">Lithographic plate</entry><entry namest="col2" nameend="col2" align="center">Sensitivity (exposure) time) (sec)</entry><entry namest="col3" nameend="col3" align="center">Development acceptability (min)</entry><entry namest="col4" nameend="col7" align="center">Burning temperature</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col5" align="center">200°C</entry><entry namest="col6" nameend="col7" align="center">260°C</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col4" align="center">Impression capacity (x10,000 sheets)</entry><entry namest="col5" nameend="col5" align="center">Degree of spreading in halftone image area</entry><entry namest="col6" nameend="col6" align="center">Impression capacity (x10,000 sheets)</entry><entry namest="col7" nameend="col7" align="center">Degree of spreading in halftone image area</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">[A]</entry><entry namest="col2" nameend="col2" align="right">40</entry><entry namest="col3" nameend="col3" align="right">6</entry><entry namest="col4" nameend="col4" align="right">25</entry><entry namest="col5" nameend="col5" align="left">A</entry><entry namest="col6" nameend="col6" align="right">40</entry><entry namest="col7" nameend="col7" align="left">B</entry></row><row><entry namest="col1" nameend="col1" align="left">[B]</entry><entry namest="col2" nameend="col2" align="right">60</entry><entry namest="col3" nameend="col3" align="right">7</entry><entry namest="col4" nameend="col4" align="right">15</entry><entry namest="col5" nameend="col5" align="left">C</entry><entry namest="col6" nameend="col6" align="right">20</entry><entry namest="col7" nameend="col7" align="left">D</entry></row><row rowsep="1"><entry namest="col1" nameend="col7" align="justify">Degree of spreading in halftone image area: A: Completely no spreading B: Almost no spreading C: Spreading occurred D: Considerable spreading occurred</entry></row></tbody></tgroup></table></tables>

0039The results summarized in Table 2 show that as compared with the lithographic plate [B] containing no phenol derivative, the lithographic plate [A] containing a phenol derivative of the present invention is almost free from scumming of non-image area and has improved impression capacity even when burning is performed at any temperature.

0040Furthermore, the lithographic plate [A] containing a phenol derivative of the present invention has higher sensitivity (is shorter in proper exposure time) than the lithographic plate [B], and the development acceptability thereof is on a level with no practical problems.

0041The above demonstrates that the phenol derivative of the present invention not only enhances sensitivity without causing a significant decrease in development acceptability, but also greatly diminishes the scumming of non-image area which is caused by burning, even at any temperature, and improves impression capacity. Thus, the derivative of the invention has exceedingly high performances.

APPLICATION EXAMPLE 2 (Photoresist)

0042A photosensitive solution [C] having the following composition was prepared. <tables id="tabl0005" num="0005"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row><entry namest="col1" nameend="col2" align="left">Photosensitive Solution [C]</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Cresol-formaldehyde novolak resin (meta/para ratio = 6:4)</entry><entry namest="col2" nameend="col2" align="left">1.0 g</entry></row><row><entry namest="col1" nameend="col1" align="left">Compound (I) of this invention, I-1</entry><entry namest="col2" nameend="col2" align="left">0.1 g</entry></row><row><entry namest="col1" nameend="col1" align="left">Triphenylsulfonium trichloromethane-sulfonate</entry><entry namest="col2" nameend="col2" align="left">20 mg</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Ethyl Cellosolve acetate</entry><entry namest="col2" nameend="col2" align="left">10 ml</entry></row></tbody></tgroup></table></tables>

0043A comparative photosensitive solution [D] was prepared separately which was the same as [C] above except that 0.1 g of bishydroxymethyl-p-cresol was used in place of the compound (I) of this invention.

0044The photosensitive solutions [C] and [D] described above were applied on a silicon wafer with a spinner and dried on a hot plate at 90°C for 2 minutes.

0045The resulting coatings were exposed using a g-line stepper (436 nm) and developed with a 2.4% aqueous solution of tetramethylammonium hydroxide to thereby obtain resists having a 0.48-µm line-and-space pattern.

0046The resist obtained from the photosensitive solution [D] had a sensitivity of 170 mJ/cm², whereas the resist obtained from the photosensitive solution [C] had a sensitivity of 100 mJ/cm². This shows that the resist obtained using the compound (I) of this invention has high sensitivity.

APPLICATION EXAMPLE 3 (Coating Composition)

0047A coating fluid [E] was prepared by dissolving 10 g of the compound represented by formula (I) which had been obtained in Synthesis Example 1 and 90 g of a phenol-formaldehyde-resol resin into 350 ml of a methanol-acetone-butyl alcohol (8:1:1) mixed solvent. Likewise, a coating fluid [F] was prepared by dissolving 10 g of bishydroxymethyl-p-cresol in place of the compound (I) and 90 g of a phenol-formaldehyde-resol resin into 350 ml of the same mixed solvent as the above-described one. Each of the coating fluids [E] and [F] was applied on a wood plate after a 50% methanol solution of benzenesulfonic acid was added thereto as a hardener in an amount of 15% based on the weight of the coating fluid.

0048After the coated samples were then allowed to stand at room temperature for 1 week, they were immersed in methanol and the film surfaces were visually examined.

0049As a result, the surface of the sample obtained using the coating fluid [F] had suffered blushing, whereas the sample obtained using the coating fluid [E] had not changed, showing that the compound (I) of the present invention has the effect of improving the solvent resistance of coating fluids.

0050Acid resistance and alkali resistance were evaluated likewise based on immersion in 50% acetic acid and in 5% aqueous sodium hydroxide solution, respectively. As a result, the coating film formed from the coating fluid [E] showed higher acid and alkali resistance than the coating film formed from the coating fluid [F].

APPLICATION EXAMPLE 4 (Lithographic Plate)

0051An aluminum plate (material, 1050) having a thickness of 0.3 mm was degreased by cleaning with trichloroethylene, and the surface of the resulting plate was grained with a nylon brush and an aqueous suspension of a 400-mesh pumice and then sufficiently washed with water. This plate was etched by immersing it in a 45°C 25% aqueous sodium hydroxide solution for 9 seconds and then washed with water. Subsequently, the plate was further immersed in 20% nitric acid for 20 seconds and then washed with water. The aluminum amount thus removed from the grained surface by etching was about 3 g/m². The resulting plate was subjected to direct-current anodizing at a current density of 15 A/dm² using 7% sulfuric acid as the electrolytic solution to deposit an oxide film on the plate in an amount of 3 g/m², and was then washed with water and dried. This aluminum plate was subsequently coated with the primer specified below and dried at 80°C for 30 seconds. The amount of the primer coat after drying was 10 mg/m². <tables id="tabl0006" num="0006"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row><entry namest="col1" nameend="col2" align="left">(Primer)</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">β-Alanine</entry><entry namest="col2" nameend="col2" align="left">0.1 g</entry></row><row><entry namest="col1" nameend="col1" align="left">Phenylphosphonic acid</entry><entry namest="col2" nameend="col2" align="left">0.05 g</entry></row><row><entry namest="col1" nameend="col1" align="left">Methanol</entry><entry namest="col2" nameend="col2" align="left">40 g</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Pure water</entry><entry namest="col2" nameend="col2" align="left">60 g</entry></row></tbody></tgroup></table></tables>

0052Further, the photosensitive liquids specified below were applied on the resulting aluminum plate and the coatings were dried at 100°C for 2 minutes to obtain positive photosensitive lithographic plates. The amount of the coating after drying was 1.8 g/m² for all the photosensitive solutions. <tables id="tabl0007" num="0007"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row><entry namest="col1" nameend="col2" align="left">Photosensitive Solution (unit; gram)</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Product of esterification of naphthoquinone-1,2-diazide-5-sulfonic acid chloride with a pyrogallol-acetone resin</entry><entry namest="col2" nameend="col2" align="right">0.90</entry></row><row><entry namest="col1" nameend="col1" align="left">Cresol-formaldehyde novolak (meta:para ratio = 6:4; weight-average molecular weight, 1,800; unreacted cresol content, 0.5%)</entry><entry namest="col2" nameend="col2" align="right">(as shown in Table 3)</entry></row><row><entry namest="col1" nameend="col1" align="left">p-Octylphenol-formaldehyde novolak</entry><entry namest="col2" nameend="col2" align="right">0.02</entry></row><row><entry namest="col1" nameend="col1" align="left">Naphthoquinone-1,2-diazide-5-sulfonic acid chloride</entry><entry namest="col2" nameend="col2" align="right">0.01</entry></row><row><entry namest="col1" nameend="col1" align="left">Phenol derivative</entry><entry namest="col2" nameend="col2" align="right">(as shown in Table 3)</entry></row><row><entry namest="col1" nameend="col1" align="left">Tetrahydrophthalic anhydride</entry><entry namest="col2" nameend="col2" align="right">0.05</entry></row><row><entry namest="col1" nameend="col1" align="left">4-(p-N,N-bis(ethoxycarbonylmethyl)phenyl)-2,6-bis(trichloromethyl)-s-triazine</entry><entry namest="col2" nameend="col2" align="right">0.02</entry></row><row><entry namest="col1" nameend="col1" align="left">4-(p-N-(p-Hydroxybenzoyl)aminophenyl)-2,6-bis(trichloromethyl)-s-triazine</entry><entry namest="col2" nameend="col2" align="right">0.02</entry></row><row><entry namest="col1" nameend="col1" align="left">Dye obtained from Victoria Pure Blue BOH by converting the counter ion into 1-naphthalenesulfonic acid</entry><entry namest="col2" nameend="col2" align="right">0.03</entry></row><row><entry namest="col1" nameend="col1" align="left">MEGAFAC F-177 (fluorine compound surfactant manufactured by Dainippon Ink and Chemicals Inc.)</entry><entry namest="col2" nameend="col2" align="right">0.15</entry></row><row><entry namest="col1" nameend="col1" align="left">Methyl ethyl ketone</entry><entry namest="col2" nameend="col2" align="right">25</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Methanol</entry><entry namest="col2" nameend="col2" align="right">1</entry></row></tbody></tgroup></table></tables><tables id="tabl0008" num="0008"><table frame="all"><title>Table 3</title><tgroup cols="4" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="39.37mm" /><colspec colnum="2" colname="col2" colwidth="39.37mm" /><colspec colnum="3" colname="col3" colwidth="39.37mm" /><colspec colnum="4" colname="col4" colwidth="39.37mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="center">Lithographic plate</entry><entry namest="col2" nameend="col2" align="center">Amount of cresol-formaldehyde novolak used (g)</entry><entry namest="col3" nameend="col4" align="center">Phenol derivative</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" align="center">Formula</entry><entry namest="col4" nameend="col4" align="center">Amount used (g)</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">[G]</entry><entry namest="col2" nameend="col2" align="char" char=".">2.1</entry><entry namest="col3" nameend="col3" align="center">hydroxymethylphenol compound (II-1)</entry><entry namest="col4" nameend="col4" align="char" char=".">0.06</entry></row><row><entry namest="col1" nameend="col1" align="left">[H]</entry><entry namest="col2" nameend="col2" align="char" char=".">2.0</entry><entry namest="col3" nameend="col3" align="center">hydroxymethylphenol compound (III-1)</entry><entry namest="col4" nameend="col4" align="char" char=".">0.06</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">[I]</entry><entry namest="col2" nameend="col2" align="char" char=".">2.1</entry><entry namest="col3" nameend="col3" align="center">none</entry><entry namest="col4" nameend="col4" align="char" char=".">-</entry></row></tbody></tgroup></table></tables>

0053With respect to these positive photosensitive lithographic plates, the sensitivity (exposure time), the development acceptability, the burning temperature, the number of prints obtained, and the degree of spreading in a halftone image area were examined in the same manner as in Application Example 1.

0054The results are shown in Table 4 below. <tables id="tabl0009" num="0009"><table frame="all"><title>Table 4</title><tgroup cols="7" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="22.50mm" /><colspec colnum="2" colname="col2" colwidth="22.50mm" /><colspec colnum="3" colname="col3" colwidth="22.50mm" /><colspec colnum="4" colname="col4" colwidth="22.50mm" /><colspec colnum="5" colname="col5" colwidth="22.50mm" /><colspec colnum="6" colname="col6" colwidth="22.50mm" /><colspec colnum="7" colname="col7" colwidth="22.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="center">Lithographic plate</entry><entry namest="col2" nameend="col2" align="center">Sensitivity (exposure) time) (sec)</entry><entry namest="col3" nameend="col3" align="center">Development acceptability (min)</entry><entry namest="col4" nameend="col7" align="center">Burning temperature</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col5" align="center">200°C</entry><entry namest="col6" nameend="col7" align="center">260°C</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col4" align="center">Impression capacity (x10,000 sheets)</entry><entry namest="col5" nameend="col5" align="center">Degree of spreading in halftone image area</entry><entry namest="col6" nameend="col6" align="center">Impression capacity (x10,000 sheets)</entry><entry namest="col7" nameend="col7" align="center">Degree of spreading in halftone image area</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">[G]</entry><entry namest="col2" nameend="col2" align="right">40</entry><entry namest="col3" nameend="col3" align="right">6</entry><entry namest="col4" nameend="col4" align="right">25</entry><entry namest="col5" nameend="col5" align="left">A</entry><entry namest="col6" nameend="col6" align="right">30</entry><entry namest="col7" nameend="col7" align="left">B</entry></row><row><entry namest="col1" nameend="col1" align="left">[H]</entry><entry namest="col2" nameend="col2" align="right">38</entry><entry namest="col3" nameend="col3" align="right">6</entry><entry namest="col4" nameend="col4" align="right">22</entry><entry namest="col5" nameend="col5" align="left">A</entry><entry namest="col6" nameend="col6" align="right">25</entry><entry namest="col7" nameend="col7" align="left">B</entry></row><row><entry namest="col1" nameend="col1" align="left">[I]</entry><entry namest="col2" nameend="col2" align="right">60</entry><entry namest="col3" nameend="col3" align="right">7</entry><entry namest="col4" nameend="col4" align="right">15</entry><entry namest="col5" nameend="col5" align="left">C</entry><entry namest="col6" nameend="col6" align="right">20</entry><entry namest="col7" nameend="col7" align="left">D</entry></row><row rowsep="1"><entry namest="col1" nameend="col7" align="justify">Degree of spreading in halftone image area: A: Completely no spreading B: Almost no spreading C: Spreading occurred D: Considerable spreading occurred</entry></row></tbody></tgroup></table></tables>

0055The results summarized in Table 4 show that as compared with the lithographic plate [I] containing no phenol derivative, the lithographic plates [G] and [H] containing phenol derivatives of the present invention are almost free from scumming of non-image area and have improved impression capacity even when burning is performed at any temperature.

0056Furthermore, the lithographic plates [G] and [H] containing phenol derivatives of the present invention have higher sensitivity (are shorter in proper exposure time) than the lithographic plate [I]. Although the plates [G] and [H] are slightly inferior to the plate [C] in development acceptability, the development acceptability of the former plates is on a level with no practical problems.

0057The above demonstrates that the phenol derivatives of the present invention not only enhance sensitivity without causing a significant decrease in development acceptability, but also greatly diminish the scumming of non-image area which is caused by burning, even at any temperature, and improve impression capacity. Thus, the derivatives of the invention have exceedingly high performances.

APPLICATION EXAMPLE 5 (Photoresist)

0058A photosensitive solution [J] having the following composition was prepared. <tables id="tabl0010" num="0010"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row><entry namest="col1" nameend="col2" align="left">Photosensitive Solution [J]</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Cresol-formaldehyde novolak resin (meta/para ratio = 6:4)</entry><entry namest="col2" nameend="col2" align="left">1.0 g</entry></row><row><entry namest="col1" nameend="col1" align="left">Compound (II) of this invention, II-1</entry><entry namest="col2" nameend="col2" align="left">0.1 g</entry></row><row><entry namest="col1" nameend="col1" align="left">Triphenylsulfonium trichloromethane-sulfonate</entry><entry namest="col2" nameend="col2" align="left">20 mg</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Ethyl Cellosolve acetate</entry><entry namest="col2" nameend="col2" align="left">10 ml</entry></row></tbody></tgroup></table></tables>

0059A comparative photosensitive solution [K] was prepared separately which was the same as [J] above except that 0.1 g of bishydroxymethyl-p-cresol was used in place of the compound (II) of this invention.

0060The photosensitive solutions [J] and [K] described above were applied on a silicon wafer with a spinner and dried on a hot plate at 90°C for 2 minutes.

0061The resulting coatings were exposed using a g-line stepper (436 nm) and developed with a 2.4% aqueous solution of tetramethylammonium hydroxide to thereby obtain resists having a 0.48-µm line-and-space pattern.

0062The resist obtained from the photosensitive solution [K] had a sensitivity of 170 mJ/cm², whereas the resist obtained from the photosensitive solution [J] had a sensitivity of 120 mJ/cm². This shows that the resist obtained using the compound (II) of this invention has high sensitivity.

APPLICATION EXAMPLE 6 (Lithographic Plate)

0063An aluminum plate (material, 1050) having a thickness of 0.3 mm was degreased by cleaning with trichloroethylene, and the surface of the resulting plate was grained with a nylon brush and an aqueous suspension of a 400-mesh pumice and then sufficiently washed with water. This plate was etched by immersing it in a 45°C 25% aqueous sodium hydroxide solution for 9 seconds and then washed with water. Subsequently, the plate was further immersed in 20% nitric acid for 20 seconds and then washed with water. The aluminum amount thus removed from the grained surface by etching was about 3 g/m². The resulting plate was subjected to direct-current anodizing at a current density of 15 A/dm² using 7% sulfuric acid as the electrolytic solution to deposit an oxide film on the plate in an amount of 3 g/m², and was then washed with water and dried. This aluminum plate was subsequently coated with the primer specified below and dried at 80°C for 30 seconds. The amount of the primer coat after drying was 10 mg/m². <tables id="tabl0011" num="0011"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row><entry namest="col1" nameend="col2" align="left">(Primer)</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">β-Alanine</entry><entry namest="col2" nameend="col2" align="left">0.1 g</entry></row><row><entry namest="col1" nameend="col1" align="left">Phenylphosphonic acid</entry><entry namest="col2" nameend="col2" align="left">0.05 g</entry></row><row><entry namest="col1" nameend="col1" align="left">Methanol</entry><entry namest="col2" nameend="col2" align="left">40 g</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Pure water</entry><entry namest="col2" nameend="col2" align="left">60 g</entry></row></tbody></tgroup></table></tables>

0064Further, the photosensitive solutions specified below were applied on the resulting aluminum plate and the coatings were dried at 100°C for 2 minutes to obtain positive photosensitive lithographic plates. The amount of the coating after drying was 1.8 g/m² for all the photosensitive solutions. <tables id="tabl0012" num="0012"><img file="EP0632003A1_D0013.tif" /></tables><tables id="tabl0013" num="0013"><img file="EP0632003A1_D0014.tif" /></tables><tables id="tabl0014" num="0014"><table frame="all"><title>Table 5</title><tgroup cols="4" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="39.37mm" /><colspec colnum="2" colname="col2" colwidth="39.37mm" /><colspec colnum="3" colname="col3" colwidth="39.37mm" /><colspec colnum="4" colname="col4" colwidth="39.37mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="center">Lithographic plate</entry><entry namest="col2" nameend="col2" align="center">Amount of cresol-formaldehyde novolak used (g)</entry><entry namest="col3" nameend="col4" align="center">Phenol derivative</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" align="center">Formula</entry><entry namest="col4" nameend="col4" align="center">Amount used (g)</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">[L]</entry><entry namest="col2" nameend="col2" align="char" char=".">2.1</entry><entry namest="col3" nameend="col3" align="left">hydroxymethylphenol compound (IV-1)</entry><entry namest="col4" nameend="col4" align="char" char=".">0.06</entry></row><row><entry namest="col1" nameend="col1" align="left">[M]</entry><entry namest="col2" nameend="col2" align="char" char=".">2.0</entry><entry namest="col3" nameend="col3" align="left">hydroxymethylphenol compound (V-1)</entry><entry namest="col4" nameend="col4" align="char" char=".">0.06</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">[N]</entry><entry namest="col2" nameend="col2" align="char" char=".">2.1</entry><entry namest="col3" nameend="col3" align="left">none</entry><entry namest="col4" nameend="col4" align="char" char=".">-</entry></row></tbody></tgroup></table></tables>

0065With respect to these positive photosensitive lithographic plates, the sensitivity (exposure time), the development acceptability, the burning temperature, the number of prints obtained, and the degree of spreading in a halftone image area were examined in the same manner as in Application Example 1.

0066The results are shown in Table 6 below. <tables id="tabl0015" num="0015"><table frame="all"><title>Table 6</title><tgroup cols="7" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="22.50mm" /><colspec colnum="2" colname="col2" colwidth="22.50mm" /><colspec colnum="3" colname="col3" colwidth="22.50mm" /><colspec colnum="4" colname="col4" colwidth="22.50mm" /><colspec colnum="5" colname="col5" colwidth="22.50mm" /><colspec colnum="6" colname="col6" colwidth="22.50mm" /><colspec colnum="7" colname="col7" colwidth="22.50mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="center">Lithographic plate</entry><entry namest="col2" nameend="col2" align="center">Sensitivity (exposure) time) (sec)</entry><entry namest="col3" nameend="col3" align="center">Development acceptability (min)</entry><entry namest="col4" nameend="col7" align="center">Burning temperature</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col5" align="center">200°C</entry><entry namest="col6" nameend="col7" align="center">260°C</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col2" /><entry namest="col3" nameend="col3" /><entry namest="col4" nameend="col4" align="center">Impression capacity (x10,000 sheets)</entry><entry namest="col5" nameend="col5" align="center">Degree of spreading in halftone image area</entry><entry namest="col6" nameend="col6" align="center">Impression capacity (x10,000 sheets)</entry><entry namest="col7" nameend="col7" align="center">Degree of spreading in halftone image area</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">[L]</entry><entry namest="col2" nameend="col2" align="right">40</entry><entry namest="col3" nameend="col3" align="right">6</entry><entry namest="col4" nameend="col4" align="right">22</entry><entry namest="col5" nameend="col5" align="left">A</entry><entry namest="col6" nameend="col6" align="right">28</entry><entry namest="col7" nameend="col7" align="left">B</entry></row><row><entry namest="col1" nameend="col1" align="left">[M]</entry><entry namest="col2" nameend="col2" align="right">38</entry><entry namest="col3" nameend="col3" align="right">6</entry><entry namest="col4" nameend="col4" align="right">22</entry><entry namest="col5" nameend="col5" align="left">A</entry><entry namest="col6" nameend="col6" align="right">28</entry><entry namest="col7" nameend="col7" align="left">B</entry></row><row><entry namest="col1" nameend="col1" align="left">[N]</entry><entry namest="col2" nameend="col2" align="right">60</entry><entry namest="col3" nameend="col3" align="right">7</entry><entry namest="col4" nameend="col4" align="right">15</entry><entry namest="col5" nameend="col5" align="left">C</entry><entry namest="col6" nameend="col6" align="right">20</entry><entry namest="col7" nameend="col7" align="left">D</entry></row><row rowsep="1"><entry namest="col1" nameend="col7" align="justify">Degree of spreading in halftone image area: A: Completely no spreading B: Almost no spreading C: Spreading occurred D: Considerable spreading occurred</entry></row></tbody></tgroup></table></tables>

0067The results summarized in Table 6 show that as compared with the lithographic plate [N] containing no phenol derivative, the lithographic plates [L] and [M] containing phenol derivatives of the present invention are almost free from scumming of non-image area and have improved impression capacity even when burning is performed at any temperature.

0068Furthermore, the lithographic plates [L] and [M] containing phenol derivatives of the present invention have higher sensitivity (are shorter in proper exposure time) than the lithographic plate [N]. Although the plates [L] and [M] are slightly inferior to the plate [C] in development acceptability, the development acceptability of the former plates is on a level with no practical problems.

0069The above demonstrates that the phenol derivatives of the present invention not only enhance sensitivity without causing a significant decrease in development acceptability, but also greatly diminish the scumming of non-image area which is caused by burning, even at any temperature, and improve impression capacity. Thus, the derivatives of the invention have exceedingly high performances.

APPLICATION EXAMPLE 7 (Photoresist)

0070Photosensitive solutions [O], [P], and [Q] having the following compositions were prepared. <tables id="tabl0016" num="0016"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row><entry namest="col1" nameend="col2" align="left">Photosensitive Solution</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Cresol-formaldehyde novolak resin (meta/para ratio = 6:4)</entry><entry namest="col2" nameend="col2" align="right">1.0 g</entry></row><row><entry namest="col1" nameend="col1" align="left">Phenol derivative</entry><entry namest="col2" nameend="col2" align="right">(as shown in Table 7)</entry></row><row><entry namest="col1" nameend="col1" align="left">Triphenylsulfonium trichloromethane-sulfonate</entry><entry namest="col2" nameend="col2" align="right">20 mg</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Ethyl Cellosolve acetate</entry><entry namest="col2" nameend="col2" align="right">10 ml</entry></row></tbody></tgroup></table></tables><tables id="tabl0017" num="0017"><table frame="all"><title>Table 7</title><tgroup cols="4" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="39.37mm" /><colspec colnum="2" colname="col2" colwidth="39.37mm" /><colspec colnum="3" colname="col3" colwidth="39.37mm" /><colspec colnum="4" colname="col4" colwidth="39.37mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" align="center">Photosensitive solution</entry><entry namest="col2" nameend="col2" align="center">Phenol derivative</entry><entry namest="col3" nameend="col3" align="center">Amount used</entry><entry namest="col4" nameend="col4" align="center">Sensitivity</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">[O]</entry><entry namest="col2" nameend="col2" align="left">hydroxymethylphenol compound (IV-1)</entry><entry namest="col3" nameend="col3" align="left">0.1 g</entry><entry namest="col4" nameend="col4" align="right">120 mJ</entry></row><row><entry namest="col1" nameend="col1" align="left">[P]</entry><entry namest="col2" nameend="col2" align="left">hydroxymethylphenol compound (V-1)</entry><entry namest="col3" nameend="col3" align="left">0.1 g</entry><entry namest="col4" nameend="col4" align="right">110 mJ</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">[Q]</entry><entry namest="col2" nameend="col2" align="left">bishydroxymethyl-p-cresol</entry><entry namest="col3" nameend="col3" align="left">0.1 g</entry><entry namest="col4" nameend="col4" align="right">170 mJ</entry></row></tbody></tgroup></table></tables>

0071The photosensitive solutions [O], [P], and [Q] described above were applied on a silicon wafer with a spinner and dried on a hot plate at 90°C for 2 minutes.

0072The resulting coatings were exposed using a g-line stepper (436 nm) and developed with a 2.4% aqueous solution of tetramethylammonium hydroxide to thereby obtain resists having a 0.48-µm line-and-space pattern.

0073The results summarized in Table 7 show that the resists obtained using the compounds (IV) and (V) of this invention have high sensitivity.

0074While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.