JP2013056967A5 - - Google Patents
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- JP2013056967A5 JP2013056967A5 JP2011194919A JP2011194919A JP2013056967A5 JP 2013056967 A5 JP2013056967 A5 JP 2013056967A5 JP 2011194919 A JP2011194919 A JP 2011194919A JP 2011194919 A JP2011194919 A JP 2011194919A JP 2013056967 A5 JP2013056967 A5 JP 2013056967A5
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- carbon atoms
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- resin composition
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Description
(式中のR1,R2はそれぞれ独立して、炭素数2〜4のアルキレン基を表し、R3〜R11はそれぞれ独立に水素原子、炭素数1〜20の脂肪族炭化水素基、脂環族炭化水素基、芳香族炭化水素基、ハロゲン原子、または炭素数1〜20のハロゲン化炭化水素基を表し、Y、Zは水素原子を表し、a、bは、2〜10の整数を、また、c、dは0〜4の整数を表す。)
前記ビスフェノール類のアルキレンオキサイド付加物におけるビスフェノール類としては、特に制限されるものではなく、例えばビスフェノールA、ビスフェノールS、フッ素化ビスフェノールA、塩素化ビスフェノールA、臭素化ビスフェノールA、4,4−ビス(ヒドロキシフェニル)スルフィド、ビス(4−ヒドロキシフェニル)メタン、ビス(4−ヒドロキシフェニル)エーテル、ビス(4−ヒドロキシフェニル)アミン、トリシクロ[5,2,1,02,6]デカンジフェノールなどが挙げられる。
(In the formula, R 1 and R 2 each independently represent an alkylene group having 2 to 4 carbon atoms, R 3 to R 11 each independently represent a hydrogen atom, an aliphatic hydrocarbon group having 1 to 20 carbon atoms, Represents an alicyclic hydrocarbon group, an aromatic hydrocarbon group, a halogen atom, or a halogenated hydrocarbon group having 1 to 20 carbon atoms, Y and Z represent a hydrogen atom , a and b are integers of 2 to 10 And c and d represent an integer of 0 to 4.)
The bisphenols in the alkylene oxide adduct of the bisphenols are not particularly limited. For example, bisphenol A, bisphenol S, fluorinated bisphenol A, chlorinated bisphenol A, brominated bisphenol A, 4,4-bis ( hydroxyphenyl) sulfide, bis (4-hydroxyphenyl) methane, bis (4-hydroxyphenyl) ether, bis (4-hydroxyphenyl) amine, such as tricyclo [5,2,1,0 2,6] decane phenol Can be mentioned.
Claims (5)
(式中のR1,R2はそれぞれ独立して、炭素数2〜12のアルキレン基を表し、R3〜R11はそれぞれ独立に水素原子、炭素数1〜20の脂肪族炭化水素基、脂環族炭化水素基、芳香族炭化水素基、ハロゲン原子、または炭素数1〜20のハロゲン化炭化水素基を表し、Y、Zは水素原子を表し、a、bは、2〜10の整数を、また、c、dは0〜4の整数を表す。) Glycol component containing an alkylene oxide adduct of the bisphenols constituting the polyester ether polyol (a1) is an active energy ray curable resin composition according to claim 1, wherein the compound represented by the following general formula (1) object.
(In the formula, R 1 and R 2 each independently represents an alkylene group having 2 to 12 carbon atoms, R 3 to R 11 each independently represent a hydrogen atom, an aliphatic hydrocarbon group having 1 to 20 carbon atoms, Represents an alicyclic hydrocarbon group, an aromatic hydrocarbon group, a halogen atom, or a halogenated hydrocarbon group having 1 to 20 carbon atoms, Y and Z represent a hydrogen atom , a and b are integers of 2 to 10 And c and d represent an integer of 0 to 4.)
(式中、E1、E2、E3、E4は、それぞれ独立に、カルボキシル基、ハロカルボニル基、炭素数1〜20のアルキルオキシカルボニル基、炭素数1〜20のシクロアルキルオキシカルボニル基、または、炭素数1〜20のアリールオキシカルボニル基を表す。また、R12、R13、R14はそれぞれ独立に、炭素数1〜20の脂肪族炭化水素基、脂環族炭化水素基、芳香族炭化水素基、ハロゲン原子、または炭素数1〜20のハロゲン化炭化水素基を表す。f、g、hはそれぞれ独立に、0〜4の整数を表す。) The active energy ray-curable resin composition according to claim 1, wherein the aromatic carboxylic acid component is an aromatic carboxylic acid component represented by the following general formula (2) and / or the following general formula (3).
(In the formula, E 1 , E 2 , E 3 and E 4 are each independently a carboxyl group, a halocarbonyl group, an alkyloxycarbonyl group having 1 to 20 carbon atoms, or a cycloalkyloxycarbonyl group having 1 to 20 carbon atoms. Or an aryloxycarbonyl group having 1 to 20 carbon atoms, and R 12 , R 13 and R 14 are each independently an aliphatic hydrocarbon group, alicyclic hydrocarbon group having 1 to 20 carbon atoms, An aromatic hydrocarbon group, a halogen atom, or a halogenated hydrocarbon group having 1 to 20 carbon atoms, and f, g, and h each independently represents an integer of 0 to 4.)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011194919A JP2013056967A (en) | 2011-09-07 | 2011-09-07 | Active energy ray-curable resin composition, and coating agent using the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011194919A JP2013056967A (en) | 2011-09-07 | 2011-09-07 | Active energy ray-curable resin composition, and coating agent using the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2013056967A JP2013056967A (en) | 2013-03-28 |
JP2013056967A5 true JP2013056967A5 (en) | 2014-07-31 |
Family
ID=48133107
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011194919A Pending JP2013056967A (en) | 2011-09-07 | 2011-09-07 | Active energy ray-curable resin composition, and coating agent using the same |
Country Status (1)
Country | Link |
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JP (1) | JP2013056967A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6388116B2 (en) * | 2014-09-17 | 2018-09-12 | 東亞合成株式会社 | Curable composition |
KR20220044113A (en) * | 2020-09-30 | 2022-04-06 | 아라까와 가가꾸 고교 가부시끼가이샤 | Active energy ray-curable resin composition and laminate |
WO2023176736A1 (en) * | 2022-03-14 | 2023-09-21 | 本州化学工業株式会社 | Novel 1,3-bis(1-methyl-1-phenylethyl)benzene compound |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6049206B2 (en) * | 1977-11-15 | 1985-10-31 | 大日本インキ化学工業株式会社 | Polymerizable prepolymer with excellent adhesion |
US4213837A (en) * | 1977-11-18 | 1980-07-22 | Ici Americas Inc. | Vinyl ester urethanes |
JPS56120719A (en) * | 1980-02-29 | 1981-09-22 | Dainippon Ink & Chem Inc | Resin composition |
JP3372073B2 (en) * | 1992-12-01 | 2003-01-27 | 日本化薬株式会社 | UV curable transmissive screen resin composition and cured product thereof |
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2011
- 2011-09-07 JP JP2011194919A patent/JP2013056967A/en active Pending
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