Unlock instant, AI-driven research and patent intelligence for your innovation.

Free-radical polymerised compound

A polymeric compound and compound technology, applied in the preparation of organic compounds, organic chemistry, chemical instruments and methods, etc., can solve problems such as fogging, difficult storage stability, and poor storage stability

Inactive Publication Date: 2006-04-12
FUJIFILM CORP
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the formation of an oxygen barrier layer causes fogging due to dark polymerization, resulting in poor storage stability
It is difficult to have high sensitivity and storage stability at the same time, and the results that can fully satisfy this requirement have not been obtained in the prior art.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Free-radical polymerised compound
  • Free-radical polymerised compound
  • Free-radical polymerised compound

Examples

Experimental program
Comparison scheme
Effect test

Synthetic example 1

[0157]

[0158] Add 2-mercaptobenzothiazole (0.1mol), 2-(bromomethyl)methyl acrylate (0.1mol), acetone (100ml) in the flask, then add triethylamine (0.1mol) dropwise under ice cooling for 1 hour ), warming up to room temperature and stirring for 2 hours. 300 ml of water was added thereto and stirred to precipitate crystals. It was filtered and dried to obtain compound A-1 with a yield of 90%. The melting point was 124.0°C, and the structure of the compound was confirmed by NMR, MASS, and IR.

Synthetic example 2

[0159]

[0160] Add 2-mercaptobenzothiazole (0.1mol), 2-(bromomethyl)acrylic acid (0.1mol), acetone (100ml) in the flask, then add triethylamine (0.1mol) dropwise for 1 hour under ice-cooling, Warm to room temperature and stir for 2 hours. 300 ml of water was added thereto, and the pH was adjusted to below 3 with 1N hydrochloric acid to precipitate crystals. Collected by filtration and dried to obtain compound A-14 with a yield of 90%. The melting point is >200°C, and the structure of the compound is confirmed by NMR, MASS, and IR.

Synthetic example 3

[0161]

[0162] Add 2-(hydroxymethyl)acrylonitrile (0.1mol), triethylamine (0.1mol), acetone (100ml) in the flask, then add undecanoic acid dichloride (0.05mol) dropwise under ice cooling for 1 hour ), warming up to room temperature and stirring for 2 hours. 300 ml of water was added thereto, and after stirring, it was extracted with ethyl acetate, and the mixture was warmed to room temperature with sulfuric acid and stirred for 2 hours. 300 ml of water was added thereto, stirred, extracted with ethyl acetate, dried over magnesium sulfate, filtered, and fully concentrated under reduced pressure to obtain compound B-8 with a yield of 80%. It was a waxy solid, and the structure of the compound was confirmed by NMR, MASS, and IR.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
melting pointaaaaaaaaaa
melting pointaaaaaaaaaa
melting pointaaaaaaaaaa
Login to View More

Abstract

A radical polymerizable compound comprising a structure represented by the following formula (I), (II) or (III), wherein X<3> represents a heterocyclic group that is connected through a hetero atom included therein; Q<1> represents a group represented by CN or COX<2>; X<2> represents a hydroxy group, a substituted oxy group, a substituted thio group, an amino group, a substituted amino group, a heterocyclic group that is connected through a hetero atom included therein or a halogen atom; X<1> represents a substituted oxy group, a, substituted amino group, a heterocyclic group that is connected through a hetero atom included therein or a halogen atom; Z<1> and Z<2> each represents a n-valent connecting group having at least 6 carbon atoms, in which the n's connecting parts are all hetero atoms; R and R, which may be the same or different, each represents a hydrogen atom, a halogen atom, a cyano group or an organic residue; or R and R, X<1> and R or R, X<3> and R or R, or Q<1> and R or R may combine with each other to form a cyclic structure; and n represents an integer of from 2 to 6.

Description

[0001] technical field of invention [0002] The present invention relates to novel radically polymerizable compounds, and more particularly, to image-forming materials that can be used in stereolithography, holography, lithographic printing plate precursors, color masks, photoresist films, and color filters , or radically polymerizable compounds in photocurable resin materials such as inks, coatings, and adhesives. In particular, it relates to radically polymerizable compounds suitable for use in photopolymerizable compositions of lithographic printing plate precursors capable of so-called direct platemaking, which uses various lasers directly with digital signals from, for example, computers, etc. plate making. Background technique [0003] Solid-state lasers, semiconductor lasers, and gas lasers that emit ultraviolet light, visible light, or infrared light with a wavelength of 300 nm to 1200 nm with high output power and compact size are now easily available, and these las...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C08F2/00C08F20/00G03F7/027C07C67/31C07C67/317C07C69/73C07C253/30C07C255/15C07C271/20C07C271/28C07D277/74C08F26/00C08F28/00G03F7/00G03F7/028
CPCC07C69/73C07D277/74C07C271/28C07C255/15C07C271/20
Inventor 国田一人
Owner FUJIFILM CORP