JP2008024694A - New 1,4-bis(2-(meth)acryloyloxyalkoxy)naphthalene compound, method for producing the same and use thereof - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a new 1,4-bis(2-(meth)acryloyloxyalkoxy)naphthalene compound, to provide a method for producing the compound and to provide uses thereof. <P>SOLUTION: The 1,4-bis(2-(meth)acryloyloxyalkoxy)naphthalene compound is represented by structural formula (1). The method for producing the compound is provided. A photopolymerization sensitizer comprises the compound as an active ingredient. A photo-curing composition comprises the photopolymerization sensitizer. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to a 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound. More specifically, the present invention relates to a 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound useful as a photopolymerization sensitizer, a production method thereof, and an application thereof.

Conventionally, in photocationic polymerization, it is known that dihydroxynaphthalene functions as a photopolymerization sensitizer (see Patent Document 1). However, the conventional dihydroxynaphthalene has a high sublimation property and has a drawback of volatilizing in the heating step when the photocurable composition is cured. For this reason, an attempt was made to introduce an acrylic group into the naphthalene skeleton, but the resulting acrylate was poor in photosensitization performance and was not desirable (see Patent Document 2).
JP-A-11-263804 Japanese Patent Laid-Open No. 62-192340

In view of such circumstances, the present inventors have intensively studied to provide a technique that eliminates these drawbacks, and as a result, have completed the present invention. That is, the object of the present invention is as follows.
1. To provide a novel compound excellent in photopolymerization sensitization performance.
2. To provide a photocurable composition containing the above compound as a photopolymerization sensitizer.
3. To provide a photocurable composition that contains the above-mentioned compound as a photopolymerization sensitizer and is less likely to volatilize (sublimate) in the heating step when photocured.

  In order to achieve the above object, the first invention provides a 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound represented by the following structural formula (1).

{In Structural Formula (1), R _{1 and} R ₂ may be the same or different and each represents a hydrogen atom, an alkyl group, an aryl group, an alkoxymethyl group, an allyloxymethyl group, or an aryloxymethyl group, R _{3 and} R ₄ may be the same or different and each represents a hydrogen atom or a methyl group, X and Y may be the same or different, and a hydrogen atom, an alkyl group, a halogen atom, a hydroxyl group, an alkoxy group, an alkylthio group , An arylthio group, a carboxyl group, or a sulfonic acid group. }

  In the second invention, 1,4-dihydroxynaphthalene compound is reacted with alkylene oxide, glycidyl ether, or halogenated alcohol (halohydrin) to give 1,4-bis (2-hydroxyalkoxy) naphthalene compound, Provided is a method for producing a 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound according to the first invention, characterized by reacting the compound with acryloyl chloride or methacryloyl chloride.

  Furthermore, the third invention provides a photopolymerization sensitizer comprising the 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound according to the first invention as an active ingredient.

  Furthermore, the fourth invention provides a photocurable composition comprising the photopolymerization sensitizer, photopolymerization initiator, and photopolymerizable monomer according to the third invention.

The present invention is as described in detail below, has the following particularly advantageous effects, and its industrial utility value is extremely large.
1. The bis (2- (meth) acryloyloxyalkoxy) naphthalene compound according to the first invention is a novel compound and exhibits excellent effects as a photopolymerization sensitizer in photoradical polymerization and photocationic polymerization.
2. According to the production method according to the second invention, the compound according to the first invention can be produced industrially advantageously.
3. The photopolymerization sensitizer according to the third invention is unlikely to volatilize (sublimate) in the heating step when the photocurable composition containing the photopolymerizable composition is cured.
4). The product after photocuring the photocurable composition according to the fourth aspect of the invention is excellent in that residual components are unlikely to elute and volatilize.

Hereinafter, the present invention will be described in detail.
The compound according to the first aspect of the present invention is a 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound represented by the structural formula (1).

Examples of the alkyl group represented by R _{1 and} R ₂ in the structural formula (1) include methyl group, ethyl group, n-propyl group, n-butyl group, n-pentyl group, n-hexyl group, and n-heptyl group. Etc. Examples of the aryl group include a phenyl group, an o-tolyl group, an m-tolyl group, a p-tolyl group, a p-methoxyphenyl group, a p-ethoxyphenyl group, and a naphthyl group. Examples of the alkoxymethyl group include a methoxymethyl group, a butoxymethyl group, a 2-ethylhexyloxymethyl group, and a 2-octyloxymethyl group. Examples of the allyloxymethyl group include an allyloxymethyl group and a methallyloxymethyl group, and examples of the aryloxymethyl group include a phenoxymethyl group.

  Examples of the alkyl group represented by X and Y in the structural formula (1) include methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, amyl, and 2-ethylhexyl. Etc. Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. Examples of the alkoxy group include a methoxy group, an ethoxy group, an n-propoxy group, an n-butoxy group, a hexyloxy group, and a 2-phenoxyethoxy group. Examples of the alkylthio group include a methylthio group, an ethylthio group, a propylthio group, a butylthio group, and a hexylthio group. Examples of the arylthio group include a phenylthio group, an o-tolylthio group, an m-tolylthio group, a p-tolylthio group, and a p-hydroxyphenylthio group.

  Specific examples of the 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound represented by the structural formula (1) include the following compounds. That is, 1,4-bis (2-acryloyloxyethoxy) naphthalene, 1,4-bis (2-methacryloyloxyethoxy) naphthalene, 1,4-bis (2-acryloyloxypropoxy) naphthalene, 1,4-bis ( 2-Methacryloyloxypropoxy) naphthalene, 1,4-bis (2-acryloyloxybutoxy) naphthalene, 1,4-bis (2-methacryloyloxybutoxy) naphthalene, 1,4-bis (2-acryloyloxyheptyloxy) naphthalene 1,4-bis (2-methacryloyloxyheptyloxy) naphthalene, 1,4-bis (2-acryloyloxyoctyloxy) naphthalene-bis (2-methacryloyloxyoctyloxy) naphthalene, 1,4-bis (2- Acryloyloxy-2-fe Ruethoxy) naphthalene, 1,4-bis (2-methacryloyloxy-2-phenylethoxy) naphthalene, 1,4-bis (2-acryloyloxy-3-methoxypropoxy) naphthalene, 1,4-bis (2-methacryloyloxy) -3-methoxypropoxy) naphthalene, 1,4-bis (2-acryloyloxy-3-butoxypropoxy)) naphthalene, 1,4-bis (2-methacryloyloxy-3-butoxypropoxy) naphthalene, 1,4-bis (2-acryloyloxy-3-allyloxypropoxy) naphthalene, 1,4-bis (2-methacryloyloxy-3-allyloxypropoxy) naphthalene, 1,4-bis (2-acryloyloxy-3- (2-ethylhexyl) Oxy) propoxy) naphthalene, 1,4-bis 2-methacryloyloxy 3- (2-ethylhexyloxy) propoxy) naphthalene, 1,4-bis (2-acryloyloxy-3-stearyloxypropoxy) naphthalene, 1,4-bis (2-methacryloyloxy-3-stearyloxy) Propoxy) naphthalene, 1,4-bis (2-acryloyloxy-3-phenoxypropoxy) naphthalene, 1,4-bis (2-methacryloyloxy-3-phenoxypropoxy) naphthalene, 2-methyl-1,4-bis ( 2-acryloyloxyethoxy) naphthalene, 2-methyl-1,4-bis (2-methacryloyloxyethoxy) naphthalene, 2-methyl-1,4-bis (2-acryloyloxypropoxy) naphthalene, 2-methyl-1, 4-bis (2-methacryloyloxyp) (Ropoxy) naphthalene, 2-methyl-1,4-bis (2-acryloyloxybutoxy) naphthalene, 2-methyl-1,4-bis (2-methacryloyloxybutoxy) naphthalene, 2-methyl-1,4-bis ( 2-acryloyloxyheptyloxy) naphthalene, 2-methyl-1,4-bis (2-methacryloyloxyheptyloxy) naphthalene, 2-methyl-1,4-bis (2-acryloyloxyoctyloxy) naphthalene-bis (2 -Methacryloyloxyoctyloxy) naphthalene and the like.

  Further, 2-methyl-1,4-bis (2-acryloyloxy-2-phenylethoxy) naphthalene, 2-methyl-1,4-bis (2-methacryloyloxy-2-phenylethoxy) naphthalene, 2-methyl- 1,4-bis (2-acryloyloxy-3-methoxypropoxy) naphthalene, 2-methyl-1,4-bis (2-methacryloyloxy-3-methoxypropoxy) naphthalene, 2-methyl-1,4-bis ( 2-acryloyloxy-3-butoxypropoxy) naphthalene, 2-methyl-1,4-bis (2-methacryloyloxy-3-butoxypropoxy) naphthalene, 2-methyl-1,4-bis (2-acryloyloxy-3) -Allyloxypropoxy) naphthalene, 2-methyl-1,4-bis (2-methacryloyloxy) 3-allyloxypropoxy) naphthalene, 2-methyl-1,4-bis (2-acryloyloxy-3- (2-ethylhexyloxy) propoxy) naphthalene, 2-methyl-1,4-bis (2-methacryloyloxy- 3- (2-ethylhexyloxy) propoxy) naphthalene, 2-methyl-1,4-bis (2-acryloyloxy-3-stearyloxypropoxy) naphthalene, 2-methyl-1,4-bis (2-methacryloyloxy- 3-stearyloxypropoxy) naphthalene, 2-methyl-1,4-bis (2-acryloyloxy-3-phenoxypropoxy) naphthalene, 2-methyl-1,4-bis (2-methacryloyloxy-3-phenoxypropoxy) Naphthalene, 2-ethyl-1,4-bis (2-acryloyl) Xyloxy) naphthalene, 2-ethyl-1,4-bis (2-methacryloyloxyethoxy) naphthalene, 2-ethyl-1,4-bis (2-methacryloyloxypropoxy) naphthalene, 2-ethyl-1,4-bis ( 2-acryloyloxybutoxy) naphthalene, 2-ethyl-1,4-bis (2-methacryloyloxybutoxy) naphthalene, 2-ethyl-1,4-bis (2-acryloyloxyheptyloxy) naphthalene, 2-ethyl-1 , 4-bis (2-methacryloyloxyheptyloxy) naphthalene, 2-ethyl-1,4-bis (2-acryloyloxyoctyloxy) naphthalene-bis (2-methacryloyloxyoctyloxy) naphthalene, 2-ethyl-1, 4-bis (2-acryloyloxy-2-phenyl ester) Toxi) naphthalene, 2-ethyl-1,4-bis (2-methacryloyloxy-2-phenylethoxy) naphthalene, 2-ethyl-1,4-bis (2-acryloyloxy-3-methoxypropoxy) naphthalene, 2- Ethyl-1,4-bis (2-methacryloyloxy-3-methoxypropoxy) naphthalene, 2-ethyl-1,4-bis (2-acryloyloxy-3-butoxypropoxy) naphthalene, 2-ethyl-1,4- Bis (2-methacryloyloxy-3-butoxypropoxy) naphthalene, 2-ethyl-1,4-bis (2-acryloyloxy-3-allyloxypropoxy) naphthalene, 2-ethyl-1,4-bis (2-methacryloyl) Oxy-3-allyloxypropoxy) naphthalene, 2-ethyl-1,4-bis (2- Acryloyloxy-3- (2-ethyl-hexyloxy) propoxy) naphthalene, 2-ethyl-1,4-bis (2-methacryloyloxy-3- (2-ethyl-hexyloxy) propoxy) naphthalene, 2-ethyl-1 , 4-Bis (2-acryloyloxy-3-stearyloxypropoxy) naphthalene, 2-ethyl-1,4-bis (2-methacryloyloxy-3-stearyloxypropoxy) naphthalene, 2-ethyl-1,4-bis Examples also include (2-acryloyloxy-3-phenoxypropoxy) naphthalene and 2-ethyl-1,4-bis (2-methacryloyloxy-3-phenoxypropoxy) naphthalene.

  Also, 2-chloro-1,4-bis (2-acryloyloxyethoxy) naphthalene, 2-chloro-1,4-bis (2-methacryloyloxyethoxy) naphthalene, 2-chloro-1,4-bis (2- Acryloyloxypropoxy) naphthalene, 2-chloro-1,4-bis (2-methacryloyloxypropoxy) naphthalene, 2-chloro-1,4-bis (2-acryloyloxybutoxy) naphthalene, 2-chloro-1,4- Bis (2-methacryloyloxybutoxy) naphthalene, 2-chloro-1,4-bis (2-acryloyloxyheptyloxy) naphthalene, 2-chloro-1,4-bis (2-methacryloyloxyheptyloxy) naphthalene, 2- Chloro-1,4-bis (2-acryloyloxyoctyloxy) naphthalene, -Chlor-1,4-bis (2-methacryloyloxyoctyloxy) naphthalene, 2-chloro-1,4-bis (2-acryloyloxy-2-phenylethoxy) naphthalene, 2-chloro-1,4-bis ( 2-methacryloyloxy-2-phenylethoxy) naphthalene, 2-chloro-1,4-bis (2-acryloyloxy-3-methoxypropoxy) naphthalene, 2-chloro-1,4-bis (2-methacryloyloxy 3- Methoxypropoxy) naphthalene, 2-chloro-1,4-bis (2-acryloyloxy-3-butoxypropoxy) naphthalene, 2-chloro-1,4-bis (2-methacryloyloxy-3-butoxypropoxy) naphthalene, 2, -Chlor-1,4-bis (2-acryloyloxy-3-allyloxypropo C) Naphthalene, 2-chloro-1,4-bis (2-methacryloyloxy-3-allyloxypropoxy) naphthalene, 2-chloro-1,4-bis (2-acryloyloxy) 3- (2-ethylhexyloxy) propoxy ) Naphthalene, 2-chloro-1,4-bis (2-methacryloyloxy-3- (2-ethylhexyloxy) propoxy) naphthalene, 2-chloro-1,4-bis (2-acryloyloxy-3-stearyloxypropoxy) ) Naphthalene, 2-chloro-1,4-bis (2-methacryloyloxy-3-stearyloxypropoxy) naphthalene, 2-chloro-1,4-bis (2-acryloyloxy-3-phenoxypropoxy) naphthalene, 2- Chlor-1,4-bis (2-methacryloyloxy-3-phenoxyp (Ropoxy) naphthalene, etc.

  Furthermore, 2-methoxy-1,4-bis (2-acryloyloxyethoxy) naphthalene, 2-methoxy-1,4-bis (2-methacryloyloxyethoxy) naphthalene, 2-methoxy-1,4-bis (2 -Acryloyloxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-methacryloyloxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-acryloyloxybutoxy) naphthalene, 2-methoxy-1,4 -Bis (2-methacryloyloxybutoxy) naphthalene, 2-methoxy-1,4-bis (2-acryloyloxyheptyloxy) naphthalene, 2-methoxy-1,4-bis (2-methacryloyloxyheptyloxy) naphthalene, 2, -Methoxy-1,4-bis (2-acryloyloxyoctyl) Ruoxy) naphthalene-bis (2-methacryloyloxyoctyloxy) naphthalene, 2-methoxy-1,4-bis (2-acryloyloxy-2-phenylethoxy) naphthalene, 2-methoxy-1,4-bis (2-methacryloyl) Oxy-2-phenylethoxy) naphthalene, 2-methoxy-1,4-bis (2-acryloyloxy-3-methoxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-methacryloyloxy-3-methoxypropoxy) ) Naphthalene, 2-methoxy-1,4-bis (2-acryloyloxy-3-butoxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-methacryloyloxy-3-butoxypropoxy) naphthalene, 2-methoxy -1,4-bis (2-acryloyloxy-3 Allyloxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-methacryloyloxy-3-allyloxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-acryloyloxy-3- (2-methoxy) -Hexyloxy) propoxy) naphthalene, 2-methoxy-1,4-bis (2-methacryloyloxy-3- (2-methoxy-hexyloxy) propoxy) naphthalene, 2-methoxy-1,4-bis (2-acryloyl) Oxy-3-stearyloxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-methacryloyloxy-3-stearyloxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-acryloyloxy-3-phenoxy) Propoxy) naphthalene, 2-methoxy-1,4-bis ( Also included are 2-methacryloyloxy-3-phenoxypropoxy) naphthalene.

  Furthermore, 2-phenoxy-1,4-bis (2-acryloyloxyethoxy) naphthalene, 2-phenoxy-1,4-bis (2-methacryloyloxyethoxy) naphthalene, 2-phenoxy-1,4-bis (2 -Acryloyloxypropoxy) naphthalene, 2-phenoxy-1,4-bis (2-methacryloyloxypropoxy) naphthalene, 2-phenoxy-1,4-bis (2-acryloyloxybutoxy) naphthalene, 2-phenoxy-1,4 -Bis (2-methacryloyloxybutoxy) naphthalene, 2-phenoxy-1,4-bis (2-acryloyloxyheptyloxy) naphthalene, 2-phenoxy-1,4-bis (2-methacryloyloxyheptyloxy) naphthalene, 2, -Phenoxy-1,4-bis (2-actyl Royloxyoctyloxy) naphthalene-bis (2-methacryloyloxyoctyloxy) naphthalene, 2-phenoxy-1,4-bis (2-acryloyloxy-2-phenylethoxy) naphthalene, 2-phenoxy-1,4-bis ( 2-methacryloyloxy-2-phenylethoxy) naphthalene, 2-phenoxy-1,4-bis (2-acryloyloxy-3-methoxypropoxy) naphthalene, 2-phenoxy-1,4-bis (2-methacryloyloxy-3- Methoxypropoxy) naphthalene, 2-phenoxy-1,4-bis (2-acryloyloxy-3-butoxypropoxy) naphthalene, 2-phenoxy-1,4-bis (2-methacryloyloxy-3-butoxypropoxy) naphthalene, 2, -Phenoxy-1,4-bi (2-acryloyloxy-3-allyloxypropoxy) naphthalene, 2-phenoxy-1,4-bis (2-methacryloyloxy-3-allyloxypropoxy) naphthalene, 2-phenoxy-1,4-bis (2-acryloyl) Oxy-3- (2-phenoxy-hexyloxy) propoxy) naphthalene, 2-phenoxy-1,4-bis (2-methacryloyloxy-3- (2-phenoxy-hexyloxy) propoxy) naphthalene, 2-phenoxy-1 , 4-Bis (2-acryloyloxy-3-stearyloxypropoxy) naphthalene, 2-phenoxy-1,4-bis (2-methacryloyloxy-3-stearyloxypropoxy) naphthalene, 2-phenoxy-1,4-bis (2-acryloyloxy-3-phenoxypro Poxy) naphthalene, 2-phenoxy-1,4-bis (2-methacryloyloxy-3-phenoxypropoxy) naphthalene and the like can also be mentioned.

  Furthermore, 2-phenylthio-1,4-bis (2-acryloyloxyethoxy) naphthalene, 2-phenylthio-1,4-bis (2-methacryloyloxyethoxy) naphthalene, 2-phenylthio-1,4-bis (2- Acryloyloxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-methacryloyloxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-acryloyloxybutoxy) naphthalene, 2-phenylthio-1,4- Bis (2-methacryloyloxybutoxy) naphthalene, 2-phenylthio-1,4-bis (2-acryloyloxyheptyloxy) naphthalene, 2-phenylthio-1,4-bis (2-methacryloyloxyheptyloxy) naphthalene, 2- Phenylthio-1,4- (2-acryloyloxyoctyloxy) naphthalene-bis (2-methacryloyloxyoctyloxy) naphthalene, 2-phenylthio-1,4-bis (2-acryloyloxy-2-phenylethoxy) naphthalene, 2-phenylthio-1,4 -Bis (2-methacryloyloxy-2-phenylethoxy) naphthalene, 2-phenylthio-1,4-bis (2-acryloyloxy-3-methoxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-methacryloyl) Oxy-3-methoxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-acryloyloxy-3-butoxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-methacryloyloxy-3-butoxypropoxy) ) Naphthalene, -Phenylthio-1,4-bis (2-acryloyloxy-3-allyloxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-methacryloyloxy-3-allyloxypropoxy) naphthalene, 2-phenylthio-1, 4-bis (2-acryloyloxy-3- (2-phenylthio-hexyloxy) propoxy) naphthalene, 2-phenylthio-1,4-bis (2-methacryloyloxy-3- (2-phenylthio-hexyloxy) propoxy) Naphthalene, 2-phenylthio-1,4-bis (2-acryloyloxy-3-stearyloxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-methacryloyloxy-3-stearyloxypropoxy) naphthalene, 2- Phenylthio-1,4-bis ( Examples also include 2-acryloyloxy-3-phenoxypropoxy) naphthalene and 2-phenylthio-1,4-bis (2-methacryloyloxy-3-phenoxypropoxy) naphthalene.

  Furthermore, 1,4-bis (2-acryloyloxyethoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-methacryloyloxyethoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-acryloyloxy) Propoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-methacryloyloxypropoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-acryloyloxybutoxy) naphthalene-2-carboxylic acid, 1,4 -Bis (2-methacryloyloxybutoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-acryloyloxyheptyloxy) naphthalene-2-carboxylic acid, 1,4-bis (2-methacryloyloxyheptyloxy) naphthalene 2-carboxylic acid, 1,4-bis (2-acryloyloxyoctyl) Oxy) naphthalene-2-carboxylic acid bis (2-methacryloyloxyoctyloxy) naphthalene-2-carboxylic acid, 1,4-bis (2-acryloyloxy-2-phenylethoxy) naphthalene-2-carboxylic acid, 1,4 -Bis (2-methacryloyloxy-2-phenylethoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-acryloyloxy-3-methoxypropoxy) naphthalene-2-carboxylic acid, 1,4-bis (2 -Methacryloyloxy-3-methoxypropoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-acryloyloxy-3-butoxypropoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-methacryloyloxy- 3-butoxypropoxy) naphthalene-2-carboxylic acid, 1,4-bis ( -Acryloyloxy-3-allyloxypropoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-methacryloyloxy-3-allyloxypropoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-acryloyl) Oxy-3- (2-ethylhexyloxy) propoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-methacryloyloxy-3- (2-ethylhexyloxy) propoxy) naphthalene-2-carboxylic acid, 1,4 -Bis (2-acryloyloxy-3-stearyloxypropoxy) naphthalene-2-carboxylic acid and the like can also be mentioned.

  Furthermore, 1,4-bis (2-methacryloyloxy-3-stearyloxypropoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-acryloyloxy-3-phenoxypropoxy) naphthalene-2-carboxylic acid, 1 , 4-Bis (2-methacryloyloxy-3-phenoxypropoxy) naphthalene-2-carboxylic acid, 1,4-bis (2-acryloyloxyethoxy) naphthalene-2-sulfonic acid, 1,4-bis (2-methacryloyl) Oxyethoxy) naphthalene-2-sulfonic acid, 1,4-bis (2-acryloyloxypropoxy) naphthalene-2-sulfonic acid, 1,4-bis (2-methacryloyloxypropoxy) naphthalene-2-sulfonic acid, 4-Bis (2-acryloyloxybutoxy) naphthalene-2-sul Acid, 1,4-bis (2-methacryloyloxybutoxy) naphthalene-2-sulfonic acid, 1,4-bis (2-acryloyloxyheptyloxy) naphthalene-2-sulfonic acid, 1,4-bis (2- Methacryloyloxyheptyloxy) naphthalene-2-sulfonic acid, 1,4-bis (2-acryloyloxyoctyloxy) naphthalene-2-sulfonic acid bis (2-methacryloyloxyoctyloxy) naphthalene-2-sulfonic acid, 1,4 -Bis (2-acryloyloxy-2-phenylethoxy) naphthalene-2-sulfonic acid, 1,4-bis (2-methacryloyloxy-2-phenylethoxy) naphthalene-2-sulfonic acid, 1,4-bis (2 -Acryloyloxy-3-methoxypropoxy) naphthalene-2-sulfonic acid, , 4-Bis (2-methacryloyloxy-3-methoxypropoxy) naphthalene-2-sulfonic acid, 1,4-bis (2-acryloyloxy-3-butoxypropoxy) naphthalene-2-sulfonic acid, 1,4-bis (2-Methacryloyloxy-3-butoxypropoxy) naphthalene-2-sulfonic acid, 1,4-bis (2-acryloyloxy-3-allyloxypropoxy) naphthalene-2-sulfonic acid, 1,4-bis (2- Methacryloyloxy-3-allyloxypropoxy) naphthalene-2-sulfonic acid, 1,4-bis (2-acryloyloxy-3- (2-ethylhexyloxy) propoxy) naphthalene-2-sulfonic acid, 1,4-bis ( 2-Methacryloyloxy-3- (2-ethylhexyloxy) propoxy) naphthalene 2-sulfonic acid, 1,4-bis (2-acryloyloxy-3-stearyloxypropoxy) naphthalene-2-sulfonic acid, 1,4-bis (2-methacryloyloxy-3-stearyloxypropoxy) naphthalene-2 -Sulfonic acid, 1,4-bis (2-acryloyloxy-3-phenoxypropoxy) naphthalene-2-sulfonic acid, 1,4-bis (2-methacryloyloxy-3-phenoxypropoxy) naphthalene-2-sulfonic acid, 1,2,4-tris (2-acryloyloxyethoxy) naphthalene, 1,2,4-tris (2-methacryloyloxyethoxy) naphthalene, 1,2,4-tris (2-acryloyloxypropoxy) naphthalene, 1, 2,4-tris (2-methacryloyloxypropoxy) naphthalene, , 2,4-Tris (2-acryloyloxybutoxy) naphthalene, 1,2,4-tris (2-methacryloyloxybutoxy) naphthalene, 1,4,5-tris (2-acryloyloxyethoxy) naphthalene, 1,4 , 5-Tris (2-methacryloyloxyethoxy) naphthalene, 1,4,5-tris (2-acryloyloxypropoxy) naphthalene, 1,4,5-tris (2-methacryloyloxypropoxy) naphthalene, 1,4,5 -Tris (2-acryloyloxybutoxy) naphthalene, 1,4,5-tris (2-methacryloyloxybutoxy) naphthalene and the like can also be mentioned.

  Representative examples of the 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound represented by the structural formula (1) are shown as the following structural formulas (2) to (6). Is.

<Second invention (manufacturing method)>
The 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound according to the first invention is first converted into a 1,4-dihydroxynaphthalene compound in the presence or absence of a base by a first reaction. In the presence or absence of this, alkylene oxide, glycidyl ether, or halogenated alcohol (halohydrin) is subjected to an addition reaction to give a 1,4-bis (2-hydroxyalkoxy) naphthalene compound. Next, by the second reaction, the 1,4-bis (2-hydroxyalkoxy) naphthalene compound obtained by the first reaction is subjected to acryloyl chloride in the presence or absence of a base, in the presence or absence of a solvent, It is obtained by reacting methacryloyl chloride to (meth) acrylation.

  Examples of the 1,4-dihydroxynaphthalene compound that can be used in the first reaction include the following compounds. That is, 1,4-dihydroxynaphthalene, 2-methyl-1,4-dihydroxynaphthalene, 2-ethyl-1,4-dihydroxynaphthalene, 2- (t-butyl) -1,4-dihydroxynaphthalene, 2-chloro- 1,4-dihydroxynaphthalene, 2-phenoxy-1,4-dihydroxynaphthalene, 2-phenoxy-1,4-dihydroxynaphthalene, 2-ethylthio-1,4-dihydroxynaphthalene, 2-phenylthio-1,4-dihydroxynaphthalene 1,4-dihydroxynaphthalene-2-carboxylic acid, 1,4-dihydroxynaphthalene-2-sulfonic acid, 1,2,4-trihydroxynaphthalene, 1,4,5-trihydroxynaphthalene and the like.

  Examples of the alkylene oxide that can be used when reacting with 1,4-dihydroxynaphthalene in the first reaction include ethylene oxide, propylene oxide, butylene oxide, 1-hexene oxide, and cyclohexene oxide. Of these, ethylene oxide, propylene oxide and butylene oxide are particularly preferred.

  Examples of the glycidyl ether that can be used when 1,4-dihydroxynaphthalene is used in the first reaction include methyl glycidyl ether, allyl glycidyl ether, n-butyl glycidyl ether, 2-ethylhexyl glycidyl ether, and 2-methyl-octyl glycidyl ether. And phenyl glycidyl ether.

  Examples of the halogenated alcohol (halohydrin) that can be used in carrying out the first reaction include the following compounds. That is, 2-bromoethanol, 2-iodoethanol, 1-chloro-2-propanol, 1-bromo-2-propanol, 2-chlorocyclohexanol, 1-chloro-3-methoxy-2-propanol and the like.

  In the first reaction, when an alkaline compound as a base is used, inorganic compounds such as sodium hydroxide, potassium hydroxide, sodium carbonate, and potassium carbonate are suitable. These alkaline compounds are usually used as an aqueous solution. Examples of the solvent in the case of using a solvent include alcohol solvents, ketone solvents, ether solvents, amide solvents, amine solvents and the like. Specific examples of alcohol solvents include methanol, ethanol, isopropyl alcohol, etc. Specific examples of ketone solvents include acetone, methyl ethyl ketone, methyl isobutyl ketone, etc. Specific examples of ether solvents include Specific examples of amide solvents include dimethylformamide and dimethylacetamide, and specific examples of amine solvents include pyridine and piperidine.

  The amount of alkylene oxide, glycidyl ether or halogenated alcohol (halohydrin) added to the 1,4-dihydroxynaphthalene compound is preferably selected in the range of 2 to 10 times the latter of the former. When the addition amount of the latter with respect to the former is 2 mol times or less, unreacted 1,4-dihydroxynaphthalene compound remains, and the purity of the product is lowered. May be difficult to precipitate, which is not preferable. A more preferable amount of the latter added to the former is in a range of 2.2 mol times to 5 mol times. When an alkali compound is present in the reaction system, it is usually preferably about 1 to 2 mol times with respect to the 1,4-dihydroxynaphthalene compound. The first reaction is usually performed at room temperature. When the progress of the reaction is slow, the reaction mixture can be heated in the range of 50 to 100 ° C. Moreover, since the red color derived from the alkali metal salt of the 1,4-dihydroxynaphthalene compound disappears as the first reaction proceeds, the progress of the reaction can be easily confirmed. After completion of the reaction, the reaction solution is cooled, and if crystals do not precipitate, water is added to the reaction solution, and the precipitated crystals are filtered and dried to give the corresponding 1,4-bis (2-hydroxyalkoxy) naphthalene compound. Can be obtained.

  In the second reaction, the 1,4-bis (2-hydroxyalkoxy) naphthalene compound obtained in the first reaction is mixed with acryloyl chloride or methacryloyl chloride in the presence or absence of a base, or in the presence or absence of a solvent. Under the reaction, (meth) acrylation is carried out to obtain a corresponding 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound.

  In the second reaction, what can be used as a raw material is 1,4-bis (hydroxylate) obtained by reacting 1,4-dihydroxynaphthalene compound with alkylene oxide, glycidyl ether or halogenated alcohol (halohydrin) in the first reaction. (2-hydroxyalkoxy) naphthalene compound. Specific examples include the following compounds. That is, 1,4-bis (2-hydroxyethoxy) naphthalene, 1,4-bis (2-hydroxypropoxy) naphthalene, 1,4-bis (2-hydroxybutoxy) naphthalene, 1,4-bis (2-hydroxy) Heptyloxy) naphthalene, 1,4-bis (2-hydroxyoctyloxy) naphthalene, 1,4-bis (2-hydroxy-2-phenylethoxy) naphthalene, 1,4-bis (2-hydroxy-3-methoxypropoxy) ) Naphthalene, 1,4-bis (2-hydroxy-3-butoxypropoxy) naphthalene, 1,4-bis (2-hydroxy-3-allyloxypropoxy) naphthalene, 1,4-bis (2-hydroxy-3-) (2-Ethylhexyloxy) propoxy) naphthalene, 1,4-bis (2-hydroxy-3-steare) Ruoxypropoxy) naphthalene, 1,4-bis (2-hydroxy-3-phenoxypropoxy) naphthalene, 2-methyl-1,4-bis (2-hydroxyethoxy) naphthalene, 2-methyl-1,4-bis ( 2-hydroxypropoxy) naphthalene, 2-methyl-1,4-bis (2-hydroxybutoxy) naphthalene, 2-methyl-1,4-bis (2-hydroxyheptyloxy) naphthalene, 2-methyl-1,4- Bis (2-hydroxyoctyloxy) naphthalene, 2-methyl-1,4-bis (2-hydroxy-2-phenylethoxy) naphthalene, 2-methyl-1,4-bis (2-hydroxy-3-methoxypropoxy) Naphthalene, 2-methyl-1,4-bis (2-hydroxy-3butoxypropoxy) naphthalene, 2-methyl 1,4-bis (2-hydroxy-3-allyloxypropoxy) naphthalene, 2-methyl-1,4-bis (2-hydroxy-3- (2-ethylhexyloxy) propoxy) naphthalene, 2-methyl-1, 4-bis (2-hydroxy-3-stearyloxypropoxy) naphthalene, 2-methyl-1,4-bis (2-hydroxy-3-phenoxypropoxy) naphthalene, and the like.

  Furthermore, 2-ethyl-1,4-bis (2-hydroxyethoxy) naphthalene, 2-ethyl-1,4-bis (2-hydroxybutoxy) naphthalene, 2-ethyl-1,4-bis (2-hydroxyheptyl) Oxy) naphthalene, 2-ethyl-1,4-bis (2-hydroxyoctyloxy) naphthalene, 2-ethyl-1,4-bis (2-hydroxy-2-phenylethoxy) naphthalene, 2-ethyl-1,4 -Bis (2-hydroxy-3-methoxypropoxy) naphthalene, 2-ethyl-1,4-bis (2-hydroxy-3butoxypropoxy) naphthalene, 2-ethyl-1,4-bis (2-hydroxy-3- Allyloxypropoxy) naphthalene, 2-ethyl-1,4-bis (2-hydroxy-3- (2-ethylhexyloxy) propoxy) Phthalene, 2-ethyl-1,4-bis (2-hydroxy-3-stearyloxypropoxy) naphthalene, 2-ethyl-1,4-bis (2-hydroxy-3-phenoxypropoxy)) naphthalene, 2-chloro- 1,4-bis (2-hydroxyethoxy) naphthalene, 2-chloro-1,4-bis (2-hydroxybutoxy) naphthalene, 2-chloro-1,4-bis (2-hydroxyheptyloxy) naphthalene, 2- Chloro-1,4-bis (2-hydroxyoctyloxy) naphthalene, 2-chloro-1,4-bis (2-hydroxy-2-phenylethoxy) naphthalene, 2-chloro-1,4-bis (2-hydroxy) -3-Methoxypropoxy) naphthalene, 2-chloro-1,4-bis (2-hydroxy-3-butoxypropoxy) naphtha 2-chloro-1,4-bis (2-hydroxy-3-allyloxypropoxy) naphthalene, 2-chloro-1,4-bis (2-hydroxy-3- (2-ethylhexyloxy) propoxy) naphthalene, Examples also include 2-chloro-1,4-bis (2-hydroxy-3-stearyloxypropoxy) naphthalene and 2-chloro-1,4-bis (2-hydroxy-3-phenoxypropoxy)) naphthalene.

  Also, 2-methoxy-1,4-bis (2-hydroxyethoxy) naphthalene, 2-methoxy-1,4-bis (2-hydroxybutoxy) naphthalene, 2-methoxy-1,4-bis (2-hydroxyheptyl) Oxy) naphthalene, 2-methoxy-1,4-bis (2-hydroxyoctyloxy) naphthalene, 2-methoxy-1,4-bis (2-hydroxy-2-phenylethoxy) naphthalene, 2-methoxy-1,4 -Bis (2-hydroxy-3-methoxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-hydroxy-3butoxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-hydroxy-3- Allyloxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-hydroxy-3- (2-methoxy-hexyl) Xyl) propoxy) naphthalene, 2-methoxy-1,4-bis (2-hydroxy-3-stearyloxypropoxy) naphthalene, 2-methoxy-1,4-bis (2-hydroxy-3-phenoxypropoxy) naphthalene, etc. Can be mentioned.

  Furthermore, 2-phenoxy-1,4-bis (2-hydroxyethoxy) naphthalene, 2-phenoxy-1,4-bis (2-hydroxypropoxy) naphthalene, 2-phenoxy-1,4-bis (2-hydroxy) Butoxy) naphthalene, 2-phenoxy-1,4-bis (2-hydroxyheptyloxy) naphthalene, 2-phenoxy-1,4-bis (2-hydroxyoctyloxy) naphthalene, 2-phenoxy-1,4-bis ( 2-hydroxy-2-phenylethoxy) naphthalene, 2-phenoxy-1,4-bis (2-hydroxy-3-methoxypropoxy) naphthalene, 2-phenoxy-1,4-bis (2-hydroxy-3-butoxypropoxy) Naphthalene, 2-phenoxy-1,4-bis (2-hydroxy-3-allyloxypropo C) Naphthalene, 2-phenoxy-1,4-bis (2-hydroxy-3- (2-phenoxy-hexyloxy) propoxy) naphthalene, 2-phenoxy-1,4-bis (2-hydroxy-3-stearyloxy) Propoxy) naphthalene, 2-phenoxy-1,4-bis (2-hydroxy-3-phenoxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-hydroxyethoxy) naphthalene, 2-phenylthio-1,4- Bis (2-hydroxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-hydroxybutoxy) naphthalene, 2-phenylthio-1,4-bis (2-hydroxyheptyloxy) naphthalene, 2-phenylthio-1, 4-bis (2-hydroxyoctyloxy) naphthalene, 2-phenyl O-1,4-bis (2-hydroxy-2-phenylethoxy) naphthalene, 2-phenylthio-1,4-bis (2-hydroxy-3-methoxypropoxy) naphthalene, 2-phenylthio-1,4-bis ( 2-hydroxy-3butoxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-hydroxy-3-allyloxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-hydroxy-3- (2 -Phenylthio-hexyloxy) propoxy) naphthalene, 2-phenylthio-1,4-bis (2-hydroxy-3-stearyloxypropoxy) naphthalene, 2-phenylthio-1,4-bis (2-hydroxy-3-phenoxypropoxy) ) Naphthalene, 1,2,4-tris (2-hydroxyxyethoxy) naphtha 1,2,4-tris (2-hydroxypropoxy) naphthalene, 1,2,4-tris (2-hydroxybutoxy) naphthalene, 1,4,5-tris (2-hydroxyethoxy) naphthalene, 1,4 , 5-tris (2-hydroxypropoxy) naphthalene, 1,4,5-tris (2-hydroxybutoxy) naphthalene and the like.

  In carrying out the second reaction, the molar ratio of acryloyl chloride or methacryloyl chloride to 1 mol of 1,4-bis (2-hydroxyalkoxy) naphthalene compound is selected in the range of 2.0 to 10.0. If the addition molar ratio of the latter to the former is less than 2.0, unreacted naphthalene compound remains, and if the addition ratio exceeds 10.0, the acryloyl chloride or methacryloyl chloride itself used in the second reaction is polymerized. The 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound, which is the target product, is difficult to separate, and the purity of the target product is lowered, which is not preferable. The addition molar ratio is more preferably in the range of 2.2 to 3.0.

  When the second reaction is performed in the presence of a base, examples of the base that can be used include trimethylamine, triethylamine, tripropylamine, tributylamine, diethylamine, dibutylamine, piperidine, pyridine, α-picoline, and γ-picoline. And organic bases such as inorganic bases such as sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium carbonate, sodium hydrogen carbonate, potassium carbonate, and potassium hydrogen carbonate. The added mole of these bases with respect to acryloyl chloride or methacryloyl chloride is preferably 1.0 to 1.5. When the addition molar ratio is less than 1, the naphthalene compound remains unreacted, and when it exceeds 1.5, the solubility of the product in the reaction solution is increased and crystallization is difficult, which is not preferable. A more preferable range of the addition molar ratio is 1 to 1.2.

  When the second reaction is carried out in the presence of a solvent, the reaction solvent that can be used is not particularly limited as long as it does not react with acryloyl chloride or methacryloyl chloride. Specifically, aromatic solvents such as benzene, toluene, o-xylene, m-xylene, ethylbenzene, i-propylbenzene, chlorobenzene, o-dichlorobenzene, methylnaphthalene, chloronaphthalene, methylene chloride, chloroform, Halogenated hydrocarbon solvents such as 1,2-dichloroethane and 1,2-dichloroethylene, amide solvents such as methylpyrrolidone, dimethylformamide and dimethylacetamide, ether solvents such as tetrahydrofuran and 1,4-dioxane, acetone, Examples thereof include ketone solvents such as methyl ethyl ketone and methyl isobutyl ketone. The reaction temperature is preferably selected in the range of 0 ° C to 80 ° C. If the temperature is 0 ° C. or lower, the reaction rate is too slow and too long, and if it is 80 ° C. or higher, polymerization of acryloyl chloride or methacryloyl chloride itself proceeds to lower the purity of the product. A more preferable reaction temperature is in the range of 20 ° C to 50 ° C. The concentration of the reactant with respect to the solvent is not particularly limited, and when it is difficult to dissolve in the solvent, the reactant can be dispersed in a slurry state and reacted.

The obtained reaction product was converted into 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound by infrared spectrum analysis, mass spectrum analysis, ¹ H-NMR spectrum analysis, etc. It can be confirmed. Both compounds show strong CO stretching vibration attributed to the ester group in the vicinity of 1720 cm ⁻¹ in the infrared spectrum analysis method, and ¹ H-NMR spectrum analysis shows a spectrum peculiar to the ABX type acrylic group. Can be easily confirmed.

  When the addition amount of alkylene oxide, glycidyl ether or halogenated alcohol (halohydrin) in carrying out the first reaction is 2.0 mol times or more with respect to 1.0 mol of 1,4-dihydroxynaphthalene compound. Depending on the reaction conditions, a compound added by 2 mol or more as shown in the following structural formula (7) is by-produced.

{In Structural Formula (7), R ₁ , R ′ ₁ , R ₂ , and R ′ ₂ represent any of a hydrogen atom, an alkyl group, an aryl group, an alkoxymethyl group, an allyloxymethyl group, and an aryloxymethyl group. However, at least _one of R ¹ and R ′ ₁ is a hydrogen atom, and at least _one of R ₂ and R ′ ₂ is a hydrogen atom. X and Y may be the same or different and each represents a hydrogen atom, an alkyl group, a halogen atom, a hydroxyl group, an alkoxy group, an alkylthio group, an arylthio group, a carboxyl group, or a sulfonic acid group. Note that m and n represent an integer of 1 or more. However, m and n are not 1 at the same time. }

  In this case, if the second reaction is continued without any particular purification, a naphthalene derivative represented by the following structural formula (8) is produced as a by-product, but when used as a photosensitizer described below, the intended polymerization These by-products may be mixed as long as they do not affect the properties of the product.

{In Structural Formula (8), R ₁ , R ′ ₁ , R ₂ , R ′ ₂ , X, Y, m and n have the same meaning as in Structural Formula (7), and R ₃ and R ₄ are hydrogen atoms Or represents a methyl group. }

<Uses of compounds>
The compound according to the first invention obtained by the above reaction, that is, 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound is a novel compound. The compound according to the first invention can be used as a photosensitizer of a photopolymerizable monomer, and a photocurable composition can be prepared by blending this compound.

  When using the compound which concerns on 1st invention as a photosensitizer, the compound which concerns on 1st invention is mix | blended with a photoinitiator with a photopolymerizable monomer, and a photocurable composition is prepared. This photocurable composition can be easily cured by light irradiation.

  The photopolymerizable monomer may be a cationic polymerizable monomer, a radical polymerizable monomer, or a mixture thereof. Examples of the photopolymerizable cationic polymerizable monomer include epoxy compounds and vinyl ethers. Common epoxy compounds include alicyclic epoxy compounds, epoxy-modified silicones, aromatic glycidyl ethers, and the like. Examples of the alicyclic epoxy compound include 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate and bis (3,4-epoxycyclohexyl) adipate. Examples of commercially available products include those manufactured by Dow Chemical Company, trade names: UVR6105, UVR6110, and the like. Examples of the epoxy-modified silicone include Toshiba GE Silicone, trade name: UV-9300, and the like. Examples of the aromatic glycidyl compound include 2,2′-bis (4-glycidyloxyphenyl) propane, and examples of the vinyl ether include methyl vinyl ether, ethyl vinyl ether, isobutyl vinyl ether, and 2-ethylhexyl vinyl ether. These cationic polymerizable monomers may be one kind or a mixture of two or more kinds.

  Examples of the photopolymerizable radical polymerizable monomer include styrene, vinyl acetate, acrylic acid, methacrylic acid, acrylonitrile, methacrylonitrile, acrylamide, acrylic ester, and methacrylic ester. Specific examples of (meth) acrylic acid esters include methyl acrylate, butyl acrylate, cyclohexyl acrylate, 2-ethylhexyl acrylate, 2-hydroxyethyl acrylate, methyl methacrylate, butyl methacrylate, and cyclohexyl methacrylate. , Tetraethylene glycol diacrylate, trimethylolpropane triacrylate, pentaerythritol triacrylate, tricyclodecane dimethanol di (meth) acrylate, 1,6-hexanediol diacrylate, epoxy acrylate, urethane acrylate, polyester acrylate, polybutadiene acrylate, Examples include polyol acrylate, polyether acrylate, silicone resin acrylate, and imide acrylate. These radical polymerizable monomers may be one kind or a mixture of two or more kinds.

  The blending amount when the compound according to the first invention is used as a photosensitizer is preferably in the range of 0.01 to 2.0% by weight with respect to the photopolymerizable monomer. If the blending amount of the photosensitizer is too small, the curing rate of the photocurable composition will be slow, and if the blending amount of the photosensitizer is too large, the physical properties of the cured product will deteriorate. . A more preferable blending amount of the photosensitizer is in the range of 0.1 to 1.0% by weight.

  As the photopolymerization initiator, an onium salt can be used. As the onium salt, a sulfonium salt or an iodonium salt is usually used. Examples of the sulfonium salt include S, S, S ′, S′-tetraphenyl-S, S ′-(4,4′-thiodiphenyl) disulfonium, bishexafluorophosphate, diphenyl-4-phenylthiophenylsulfonium hexa Examples thereof include fluorophosphate and triphenylsulfonium hexafluorophosphate. As a product marketed, the Dow Chemical company make and brand name: UVI6992 are mentioned, for example. On the other hand, examples of the iodonium salt include 4-isobutylphenyl-4′-methylphenyliodonium hexafluorophosphate, bis (dodecylphenyl) iodonium hexafluoroantimonate, 4-isopropylphenyl-4′-methylphenyliodonium tetrakispentafluorophenylborate. Is mentioned. Examples of commercially available products include Ciba Specialty Chemicals, trade name: Irgacure 250, Rhodia, trade name: 2074, and the like. The addition amount of the initiator to the photopolymerizable monomer is preferably in the range of 0.01 to 5.0% by weight, and more preferably in the range of 0.05 to 2.0% by weight.

  The photocurable composition according to the fourth invention of the present invention is composed of a photopolymerizable monomer and the compound according to the first invention from a photosensitizer and a photopolymerization initiator, and further does not impair the effects of the present invention. Addition of various resins such as diluents, colorants, organic or inorganic fillers, leveling agents, surfactants, antifoaming agents, thickeners, flame retardants, antioxidants, stabilizers, lubricants, plasticizers, etc. An agent can be mix | blended in a normal use range.

  Diluents include epoxy-based diluents such as epoxy acrylate, oxetane-based diluents such as oxacyclobutane, vinyl ether-based diluents, (meth) acrylic monomer-based diluents, and the like. Examples of the colorant include a blue pigment, a red pigment, a white pigment, and a black pigment. Examples of the black pigment include carbon black, acetylene black, lamp black, and aniline black. Examples of yellow pigments include yellow lead, zinc yellow, cadmium yellow, yellow iron oxide, mineral fast yellow, nickel titanium yellow, navel yellow, naphthol yellow S, Hansa Yellow G, Hansa Yellow 10G, Benzidine Yellow G, and Benzidine Yellow. GR, quinoline yellow lake, permanent yellow NCG, tartrazine lake and the like.

  Examples of red pigments include bengara, cadmium red, red lead, mercury cadmium sulfide, permanent red 4R, resol red, lake red D brilliant carmine 6B, eosin lake, rhodamine lake B, alizarin lake, brilliant carmine 3B, and the like. . Examples of the blue pigment include bitumen, cobalt blue, alkali blue lake, Victoria blue lake, phthalocyanine blue, metal-free phthalocyanine blue, phthalocyanine blue partial chloride, first sky blue, and induslen blue BC. Examples of white pigments include zinc white, titanium oxide, antimony white, and zinc sulfide. Examples of other pigments include barite powder, barium carbonate, clay, silica, white carbon, talc, and alumina white.

The photocurable composition according to the fourth invention of the present invention can be cured by irradiating the coating film with light in the ultraviolet region after coating it on a substrate.
The application method is not particularly limited as long as it can apply the photocurable composition onto the substrate, and can be performed by a bar coating method, a spray coating method, or the like. The base material may be any of a steel plate, a printing plate, a film, paper, an aluminum foil or the like that has a flat appearance, a curved surface, or a lump. The photocurable composition applied on the substrate can be quickly cured, particularly by irradiating light in the wavelength region of 300 to 400 nm. The light source in this case is not particularly limited as long as it is a light source capable of emitting light in the wavelength region of 300 to 400 nm. For example, a high pressure mercury lamp, an ultrahigh pressure mercury lamp, a halogen lamp, sunlight, a metal halide lamp, a xenon lamp. , Ultraviolet (UV) LED lamps, H lamps manufactured by Fusion, D lamps, and the like.

In the case of photo radical curing, light irradiation is preferably performed in the absence of oxygen. When irradiated in the presence of oxygen, the progress of the photopolymerization reaction is inhibited by oxygen, and the surface of the cured film cannot be made sticky (tack), and it is necessary to add a large amount of initiator. Examples of the photocuring method in the absence of oxygen include a method performed in an inert gas atmosphere such as nitrogen gas and helium gas. It is also possible to employ a method of covering with an oxygen-impermeable film and irradiating light from above the film.
In addition, confirmation of completion of photocuring can be performed by a tack (stickiness) free test (a finger touch test). In this tack-free test, the cured film on the surface of a substrate such as a film is touched with a fingertip, the tack is confirmed, and the time until tack of the cured film disappears is called “tack-free time” (light irradiation time). The slowness of the curing reaction can be determined by the length of this time. A shorter “tack free time” means a faster cure rate.

  In order to apply and cure the photocurable composition according to the fourth invention of the present invention on, for example, a film surface, the following procedure is performed. That is, the photocurable composition is applied to the film surface by a bar coating method. When the base material is a film, it is applied using a bar number coater with a rod number such that the thickness of the coating film is usually several μm to several tens of μm. The photopolymerizable composition containing the photopolymerizable monomer can be rapidly cured by irradiating the light of the above-described light source onto the coated product thus obtained.

  EXAMPLES Hereinafter, although this invention is demonstrated in detail based on an Example, this invention is not limited to the following description examples, unless the meaning is exceeded.

[Example 1]
<Synthesis of 1,4-bis (2-acryloyloxyethoxy) naphthalene>
(First reaction)
In a three-neck flask equipped with a stirrer and a thermometer and having a capacity of 200 ml, 5.0 g (31 mmol) of naphthalene-1,4-diol was dissolved in 50 ml of dimethylformamide, and then 15.6 g (144 mmol) of bromoethanol was charged. . Next, 12.9 g of potassium carbonate was added, and the contents of the flask were stirred and mixed at 90 ° C. After completion of the reaction, 100 ml of pure water was added to the reaction solution to precipitate crystals. The precipitated crystals were separated by filtration, and the obtained crystals were washed with 20 ml of pure water and subsequently dried under reduced pressure to obtain 3.3 g of white powdery 1,4-bis (2-hydroxyethoxy) naphthalene. The yield of the product with respect to naphthalene-1,4-diol is 42 mol%, and the melting point of the product (the melting point measuring device manufactured by Gelen Camp, based on JIS K0064, model: measured by MFB-595) is 108-109 ° C.

(Second reaction)
In a three-necked flask equipped with a stirrer and a thermometer and having a capacity of 50 ml, 1.5 g (6 mmol) of 1,4-bis (2-hydroxyethoxy) naphthalene was dispersed in 10 g of acetone, and 1.1 g of acryloyl chloride ( 12 mmol). Then, 1.2 g (12 mmol) of triethylamine was added while the three-necked flask was immersed in ice water and cooled. After the addition of triethylamine, the reaction solution was weakly exothermic and became a homogeneous solution, but the triethylamine hydrochloride immediately precipitated. After returning the internal temperature of the three-necked flask to room temperature and stirring for 30 minutes, 10 g of water was added to dissolve all the precipitated hydrochloride. When the solution was allowed to stand for 30 minutes, a viscous oil precipitated, and the precipitate was separated. Next, 15 ml of n-hexane was added to the precipitate to form a slurry, and this slurry was left in a refrigerator for 6 hours. Since the oil solidified, the temperature in the three-necked flask was returned to room temperature, made into a slurry again, suction filtered and dried to obtain 0.9 g of colorless crystals. The yield of the product based on 1,4-bis (2-hydroxyethoxy) naphthalene was 40 mol%.

About the colorless crystals obtained, (1) Melting point (measured by Melencamp, melting point measuring device, model: MFB-595 based on JIS K0064) or refractive index (Atago refractometer, model: 1T) ), (2) IR spectrum by infrared (IR) spectrophotometer (manufactured by JASCO Corporation, model: IR-810), (3) nuclear magnetic resonance apparatus (NMR) (manufactured by JEOL Ltd., model: GSX FT NMR Spectrometer) ¹ H-NMR analysis, (4) Mass spectrum (manufactured by Shimadzu Corporation, mass spectrometer, model: using GCMS-QP5000), and the like were measured.

The measurement results are as follows, and it was confirmed that the colorless crystals were 1,4-bis (2-acryloyloxyethoxy) naphthalene.
(1) Melting point: 58-59 ° C.
(2) Infrared (IR) absorption spectrum (KBr, cm ⁻¹ ): absorption at wavelengths such as 742, 770, 806, 973, 1068, 1100, 1155, 1198, 1237, 1268, 1406, 1452, 1590, 1728 Admitted.
(3) ¹ H-NMR (CDCl ₃ , ppm): δ = 4.31 (t, 4H, methylene), 4.62 (t, 4H, methylene), 5.84 (dd, 2H, vinyl group), 6.17 (dd, 2H, vinyl group), 6.46 (dd, 2H, vinyl group), 6.68 (s, 2H, naphthalene ring), 7.42-7.55 (m, 2H, naphthalene ring) ), 8.14-8.26 (m, 2H, naphthalene ring).
(4) Mass spectrum: (EI-MS) m / z = 356 (M ^<+> ).

[Example 2]
<Synthesis of 1,4-bis (2-methacryloyloxyethoxy) naphthalene>
(Second reaction)
In a three-necked flask equipped with a stirrer and a thermometer and having a capacity of 50 ml, 1.5 g (6 mmol) of 1,4-bis (2-hydroxyethoxy) naphthalene was dispersed in 10 g of acetone, and 1.3 g of methacryloyl chloride ( 12 mmol) was charged. Then, 1.2 g (12 mmol) of triethylamine was added while the three-necked flask was immersed in ice water and cooled. After the addition of triethylamine, the reaction solution became weak and exothermic and became a homogeneous solution, but triethylamine hydrochloride immediately precipitated. After returning the internal temperature of the three-necked flask to room temperature and stirring for 30 minutes, 10 g of water was added to dissolve all of the precipitated hydrochloride. When the solution was allowed to stand at room temperature for 30 minutes, a viscous oil precipitated, and the precipitate was separated. Next, 15 ml of n-hexane was added to form a slurry, which was left in a refrigerator for 6 hours. Since the oil solidified, the temperature in the three-necked flask was returned to room temperature, and it was made into a slurry again, and suction filtered and dried to obtain 1.0 g of white crystals. The yield of the product based on 1,4-bis (2-hydroxyethoxy) naphthalene was 45 mol%.

About the obtained white crystal | crystallization, characteristics, such as above-mentioned (1)-(4), were measured. The measurement results are as follows, and it was confirmed that the white crystals were 1,4-bis (2-methacryloyloxyethoxy) naphthalene.
(1) Melting point: 75-76 ° C.
(2) Infrared (IR) absorption spectrum (KBr, cm ⁻¹ ): Absorption is observed at wavelengths such as 762, 935, 1100, 1170, 1240, 1275, 1320, 1383, 1450, 1590, 1625, 1715, 2950, etc. It was.
(3) ¹ H-NMR (CDCl ₃ , ppm): δ = 1.96 (s, 6H, methyl group), 4.34 (t, 4H, methylene), 4.62 (t, 4H, methylene), 5.59 (t, 2H, vinyl group), 6.16 (s, 2H, vinyl group), 6.72 (s, 2H, naphthalene ring), 7.48-7.53 (m, 2H, naphthalene ring) ), 8.15-8.25 (m, 2H, naphthalene ring).
(4) Mass spectrum: (EI-MS) m / z = 384 (M ^<+> ).

[Example 3]
<Synthesis of 1,4-bis (2-acryloyloxypropoxy) naphthalene>
(First reaction)
A three-neck flask equipped with a stirrer and a thermometer and having a capacity of 50 ml was charged with 3.2 g (20 mmol) of naphthalene-1,4-diol dissolved in 10 ml of methanol. Next, 7 g (120 mmol) of propylene oxide and an aqueous solution in which 0.4 g of sodium hydroxide was dissolved in 7 ml of water were charged. Immediately after the sodium hydroxide aqueous solution was charged, the temperature of the reaction solution slightly increased (about 5 ° C.). After completion of the reaction, the reaction solution was allowed to stand for 2 days, and crystals were precipitated at the bottom of the three-necked flask. 10 g of a 10% strength aqueous sulfuric acid solution was added to the reaction solution, and suction filtration and drying were carried out to obtain 4.0 g of 1,4-bis (2-hydroxypropoxy) naphthalene in the form of an off-white powder. The yield of the product based on naphthalene-1,4-diol was 72 mol%. The melting point of the product (measurement method is the same as above) was 108-110 ° C.

(Second reaction)
2.8 g (10 mmol) of 1,4-bis (2-hydroxypropoxy) naphthalene obtained in the first reaction was dispersed in 20 g of acetone in a three-necked flask equipped with a stirrer and a thermometer and having a capacity of 100 ml. Then, 1.8 g (20 mmol) of acryloyl chloride was further charged. Next, 2 g (20 mmol) of triethylamine was charged while the three-necked flask was immersed in ice water and cooled. Immediately after the triethylamine was charged, the temperature of the reaction solution slightly increased (about 3 ° C.). The reaction solution became a homogeneous solution, but triethylamine hydrochloride immediately precipitated. The temperature of the reaction solution was returned to room temperature, stirred for 30 minutes, and 20 g of water was added. The precipitated hydrochloride was dissolved in the reaction solution. When the reaction solution was allowed to stand at room temperature for 1 hour, a viscous oily substance was precipitated, and the precipitate was separated from the reaction solution. Next, 30 ml of n-hexane was added to the separated oily substance to form a slurry, and left in a refrigerator adjusted to a temperature of 0 ° C. for 48 hours. As a result, the oily substance solidified. The internal temperature of the three-necked flask containing the solidified oil-like material was returned to room temperature, made into a slurry again, suction filtered and dried to obtain 1.3 g of colorless crystals. The yield of the product based on 1,4-bis (2-hydroxypropoxy) naphthalene was 33 mol%.

With respect to the obtained colorless crystals, the characteristics such as (1) to (4) described above were measured. The measurement results are as follows, and it was confirmed that the colorless crystals were 1,4-bis (2-acryloyloxypropoxy) naphthalene.
(1) Melting point: 72-74 ° C.
(2) Infrared (IR) absorption spectrum (KBr, cm ⁻¹ ): 2980, 2930, 1722, 1632, 1588, 1454, 1380, 1290, 1276, 1240, 1200, 1160, 1100, 1080, 966, 961, 800 , 776, 750, etc., absorption was recognized.
(3) ¹ H-NMR (CDCl ₃ , 270 MHz) δ: 1.50 (d, J = 8 Hz, 6H), 4.12 (d, J = 5 Hz, 2H), 4.18 (d, J = 5 Hz) , 2H), 5.50 (m, 2H), 5.85 (d, J = 11 HZ, 2H), 6.16 (dd, J ₁ = 11 Hz, J ₂ = 17 Hz, 2H), 6.45 (d , J = 17 Hz, 2H), 6.70 (s, 2H), 7.50 (m, 2H), 8.20 (m, 2H)
(4) Mass spectrum: (EI-MS) m / z = 384 (M ⁺ )

[Example 4]
<Synthesis of 1,4-bis (2-acryloyloxybutoxy) naphthalene>
(First reaction)
A 300 ml three-necked flask equipped with a condenser, a thermometer and a stirrer was charged with a solution of 8 g (50 mmol) of 1,4-dihydroxynaphthalene in 40 ml of dimethylacetamide and then 4.8 g of sodium hydroxide under a nitrogen atmosphere. A solution in which (120 mmol) was dissolved in 30 m of water was charged. After stirring the reaction solution for 10 minutes, a solution of 18 g (250 mmol) of butylene oxide dissolved in 25 ml of dimethylacetamide was added. The three-necked flask was immersed in an oil bath at 60 ° C. and heated and stirred for 5 hours under a nitrogen atmosphere. After stirring for 5 hours, the internal temperature of the three-necked flask was cooled to room temperature, and 10% sulfuric acid aqueous solution was added to acidify the pH of the reaction solution. As a result, a black oily substance precipitated. The supernatant water was discarded, and the oily substance precipitated at the bottom of the flask was washed twice with 30 ml of water to obtain 7.4 g of a reddish brown oily substance. The yield of the product based on 1,4-dihydroxynaphthalene was 48 mol%.

The characteristics such as the above (2) to (3) were measured for the reddish brown oily substance. The measurement results are as follows, and it was confirmed that the product was 1,4-bis (2-hydroxybutoxy) naphthalene.
(2) Infrared (IR) absorption spectrum (KBr, cm ⁻¹ ): 3350, 3060, 2960, 2920, 2870, 1620, 1590, 1455, 1380, 1270, 1230, 1090, 1018, 920, 876, 800, 760 , Absorption at wavelengths such as 600 was observed.
(3) ¹ H-NMR (CDCl 3, 270 MH): δ 1.08 (6H, t, J = 8 Hz), 1.66 to 1.80 (4H, m), 2.39 (2H, bs); 95-4.06 (2H, m), 4.06-4.16 (4H, m), 6.70 (2H, s), 7.48-7.60 (2H, m), 8.17- 8.28 (2H, m).

(Second reaction)
A three-neck flask equipped with a thermometer and a stirrer and having a capacity of 300 ml was charged with a solution of 5.8 g (19 mmol) of 1,4-bis (2-hydroxybutoxy) naphthalene in 50 ml of methylene chloride under a nitrogen atmosphere, and then chlorinated. 5.4 g (60 mmol) of acryloyl was charged. While the three-necked flask was immersed in ice water and cooled, a solution in which 6.1 g (60 mmol) of triethylamine was dissolved in 25 m of methylene chloride was charged. After stirring at 0 ° C. for 2 hours, the cooling of the three-necked flask with ice water was stopped, and the mixture was left at room temperature overnight. Since triethylamine hydrochloride crystals floated on the surface of the reaction solution, 30 ml of water was added to the reaction solution to dissolve the crystals to form two layers. The lower methylene chloride layer was separated, 10 g of anhydrous sodium sulfate was added to the methylene chloride layer, and the mixture was allowed to stand overnight and dried. Next, the methylene chloride solution was treated with an alumina column, and the effluent was concentrated to obtain 4.1 g of a light khaki oil. The yield of the product based on 1,4-bis (2-hydroxybutoxy) naphthalene was 53 mol%.

The characteristics such as (1) to (4) above were measured for the light khaki oily matter. The measurement results are as follows, and it was confirmed that the product was 1,4-bis (2-acryloyloxybutoxy) naphthalene.
(1) Refractive index: 1.551.
(2) Infrared (IR) absorption spectrum (KBr, cm ⁻¹ ): 2960, 2930, 2870, 1720, 1622, 1592, 1456, 1400, 1380, 1270, 1235, 1172, 1152, 1095, 1042, 980, 800 , Absorption at wavelengths such as 760 was observed.
(3) ¹ H-NMR (CDCl3, 270MH): δ 1.05 (6H, t, J = 8 Hz), 1.80-2.00 (4H, m), 4.21 (4H, d, J = 7 Hz) ), 5.34-5.46 (2H, m), 5.86 (2H, d, J = 11 Hz), 6.17 (2H, dd, J1 = 11 Hz, J2 = 17 Hz), 6.46 (2H) , D, J = 17 Hz), 6.70 (2H, S), 7.44-7.57 (2H, m), 8.14-8.24 (2H, m).
(4) Mass spectrum: (EI-MS) m / z = 412 (M ^<+> ).

[Example 5]
<Synthesis of 1,4-bis (2-acryloyloxy-3-butoxypropoxy) naphthalene>
(First reaction)
A 300 ml three-necked flask equipped with a condenser, a thermometer, and a stirrer was charged with a solution of 8 g (50 mmol) of 1,4-dihydroxynaphthalene in 40 ml of dimethylacetamide, and 4.8 g of caustic soda (120 g) under a nitrogen atmosphere. Millimoles) of 30m water. After stirring for 10 minutes, a solution in which 15.5 g (120 mmol) of butyl glycidyl ether was dissolved in 25 ml of dimethylacetamide was then charged, and the three-necked flask was immersed in an oil bath at 60 ° C. and heated and stirred for 10 hours in a nitrogen atmosphere. did. After stirring for 10 hours, the internal temperature of the three-necked flask was cooled to room temperature, and 10% sulfuric acid aqueous solution was added to acidify the pH of the reaction solution. As a result, a black brown oily substance precipitated. The supernatant water was discarded, and the oily substance at the bottom of the three-neck flask was washed twice with 30 ml of water to obtain 8.6 g of a brown oily substance. The yield of the product based on 1,4-dihydroxynaphthalene was 40 mol%.

With respect to the brown oily material, the above characteristics (2) to (3) were measured. The measurement results were as follows, and it was confirmed that the product was 1,4-bis (2-hydroxy-3-butoxypropoxy) naphthalene.
(2) Infrared (IR) absorption spectrum (KBr, cm ⁻¹ ): Absorption at wavelengths such as 3350, 2950, 2920, 2860, 1620, 1590, 1455, 1380, 1270, 1234, 1084, 1020, 800, 760 Admitted.
(3) ¹ H-NMR (CDCl 3, 270 MH): δ 0.92 (6H, t, J = 8 Hz), 1.30-1.46 (4H, m), 1.52-1.68 (4H, m ), 3.54 (4H, t, J = 7 Hz), 3.62-3.77 (4H, m), 4.1-4.2 (4H, m), 4.24-4.35 (2H) M), 6.73 (2H, s), 7.43-7.57 (2H, m), 8.16-8.25 (2H, m).

(Second reaction)
A 300 ml three-necked flask equipped with a thermometer and a stirrer was charged with a solution of 8.4 g (20 mmol) of 1,4-bis (2-hydroxy-3-butoxypropoxy) naphthalene in 50 ml of methylene chloride under a nitrogen atmosphere. Subsequently, 5.4 g (60 mmol) of acryloyl chloride was charged. Further, a solution prepared by dissolving 6.1 g (60 mmol) of triethylamine in 25 m of methylene chloride was added while cooling the three-necked flask in ice water. After stirring at a temperature of 0 ° C. for 2 hours, cooling of the three-necked flask with ice water was stopped, and the mixture was allowed to stand at room temperature overnight. On the next day, crystals of triethylamine hydrochloride floated on the surface of the reaction solution, so 30 ml of water was added to the reaction solution to dissolve the crystals into two layers. The lower methylene chloride layer was separated, 10 g of anhydrous sodium sulfate was added to the methylene chloride layer, and the mixture was allowed to stand overnight and dried. Next, the methylene chloride solution was treated with an alumina column, and the resulting effluent was concentrated to obtain 6.9 g of a light khaki oil. The yield of the product based on 1,4-bis (2-hydroxy-3-butoxypropoxy) naphthalene was 65 mol%.

The characteristics such as (1) to (4) above were measured for the light khaki oily matter. The measurement results are as follows, and it was confirmed that the product was 1,4-bis (2-acryloyloxy-3-butoxypropoxy) naphthalene.
(1) Refractive index: 1.533.
(2) Infrared (IR) absorption spectrum (KBr, cm ⁻¹ ): 2950, 2930, 2860, 1720, 1626, 1592, 1462, 1400, 1380, 1262, 1236, 1192, 1146, 1090, 980, 802, 760 Absorption was observed at such wavelengths.
(3) 1H-NMR (CDCl3, 270MH): δ 0.90 (6H, t, J = 8 Hz), 1.25-1.45 (4H, m), 1.48-1.64 (4H, m) 3.40-3.60 (4H, m), 3.80 (4H, d, J = 7 Hz), 4.27-4.38 (4H, m), 5.50-5.62 (2H, m), 5.86 (2H, d, J = 11 Hz), 6.20 (2H, dd, J1 = 11 Hz, J2 = 17 Hz), 6.49 (2H, d, J = 17 hz), 6.72 ( 2H, s), 7.44-7.57 (2H, m), 8.14-8, 23 (1H, m).
(4) Mass spectrum: (EI-MS) m / z = 528 (M ^<+> ).

[Evaluation Test-1 as Photopolymerization Sensitizer]
The method described in Example 1 in 100 parts by weight of trimethylolpropane triacrylate as a monomer and 2 parts by weight of tolyl-i-butylphenyliodonium hexafluorophosphate (manufactured by Ciba Specialty, trade name: Irgacure 250) 1.0 parts by weight of 1,4-bis (2-acryloyloxyethoxy) naphthalene synthesized in Step 1 was added and mixed uniformly to obtain a photocurable composition. This photocurable composition was applied to the surface of a polyester film (trade name: Lumirror, film thickness: 100 μm) by a bar coater so that the film thickness was 12 μm. Subsequently, a high pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was irradiated in a nitrogen atmosphere. The tack free time (curing time) until tackiness disappears (curing time) (see the description in paragraph 0058 for details of the measurement method) was 1.8 minutes.

[Evaluation Test-2 as Photopolymerization Sensitizer]
The method described in Example 2 in 100 parts by weight of trimethylolpropane triacrylate as a monomer and 2 parts by weight of tolyl-i-butylphenyliodonium hexafluorophosphate (manufactured by Ciba Specialty, trade name: Irgacure 250) 1.0 parts by weight of 1,4-bis (2-methacryloyloxyethoxy) naphthalene synthesized in Step 1 was added and mixed uniformly to obtain a photocurable composition. This photocurable composition was applied to a surface of a polyester film (trade name: Lumirror, film thickness 100 μm) by a bar coater so as to have a film thickness of 12 μm. Subsequently, a high pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was irradiated in a nitrogen atmosphere. The tack free time (curing time) until tackiness disappears was 2.5 minutes.

[Evaluation Test-3 as a Photopolymerization Sensitizer]
The method described in Example 3 in 100 parts by weight of trimethylolpropane triacrylate as a monomer and 2 parts by weight of tolyl-i-butylphenyliodonium hexafluorophosphate (trade name: Irgacure 250, manufactured by Ciba Specialty) 1.0 parts by weight of 1,4-bis (2-acryloyloxypropoxy) naphthalene synthesized in Step 1 was added and mixed uniformly to obtain a photocurable composition. This photocurable composition was applied to a surface of a polyester film (trade name: Lumirror, film thickness 100 μm) by a bar coater so as to have a film thickness of 12 μm. Subsequently, a high pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was irradiated in a nitrogen atmosphere. The tack free time (curing time) until tackiness disappears was 3.3 minutes.

[Evaluation Test 4 as Photopolymerization Sensitizer]
The method described in Example 4 in which 100 parts by weight of trimethylolpropane triacrylate as a monomer is 2 parts by weight of tolyl-i-butylphenyliodonium hexafluorophosphate (trade name: Irgacure 250, manufactured by Ciba Specialty). 1.0 parts by weight of 1,4-bis (2-acryloyloxybutoxy) naphthalene synthesized in Step 1 was added and mixed uniformly to obtain a photocurable composition. This photocurable composition was applied to a surface of a polyester film (trade name: Lumirror, film thickness 100 μm) by a bar coater so as to have a film thickness of 12 μm. Subsequently, a high pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was irradiated in a nitrogen atmosphere. The tack free time (curing time) until the stickiness (tack) disappeared was 2.0 minutes.

[Evaluation Test-5 as a Photopolymerization Sensitizer]
The method described in Example 5 in which 100 parts by weight of trimethylolpropane triacrylate as a monomer is 2 parts by weight of tolyl-i-butylphenyliodonium hexafluorophosphate (trade name: Irgacure 250, manufactured by Ciba Specialty). 1.0 parts by weight of 1,4-bis (2-acryloyloxy-3-butoxypropoxy) naphthalene synthesized in Step 1 was added and mixed uniformly to obtain a photocurable composition. This photocurable composition was applied to a surface of a polyester film (trade name: Lumirror, film thickness 100 μm) by a bar coater so as to have a film thickness of 12 μm. Subsequently, a high pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was irradiated in a nitrogen atmosphere. The tack free time (curing time) until tackiness disappears was 2.5 minutes.

[Evaluation Test-6 as a Photopolymerization Sensitizer]
2 parts by weight of tolyl-i-butylphenyliodonium hexafluorophosphate (product name: Irgacure 250) manufactured by Dow Chemical Co., Ltd., which is an alicyclic epoxy compound, as a monomer Then, 1.0 part by weight of 1,4-bis (2-acryloyloxyethoxy) naphthalene synthesized by the method described in Example 1 was added and mixed uniformly to obtain a photocurable composition. This photocurable composition was applied to a surface of a polyester film (trade name: Lumirror, film thickness 100 μm) by a bar coater so as to have a film thickness of 12 μm. Then, a high pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was irradiated. The tack free time (curing time) until tackiness disappears was 2.3 minutes.

[Evaluation Test-7 as Photopolymerization Sensitizer]
2 parts by weight of tolyl-i-butylphenyliodonium hexafluorophosphate (product name: Irgacure 250) manufactured by Dow Chemical Co., Ltd., which is an alicyclic epoxy compound as a monomer, manufactured by Dow Chemical Co. Part, 1.0 part by weight of 1,4-bis (2-methacryloyloxyethoxy) naphthalene synthesized by the method described in Example 2 was added and mixed uniformly to obtain a photocurable composition. This photocurable composition was applied to a surface of a polyester film (trade name: Lumirror, film thickness 100 μm) by a bar coater so as to have a film thickness of 12 μm. Then, a high pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was irradiated. The tack free time (curing time) until tackiness disappears was 2.2 minutes.

[Evaluation Test -8 as a Photopolymerization Sensitizer]
2 parts by weight of tolyl-i-butylphenyliodonium hexafluorophosphate (product name: Irgacure 250) manufactured by Dow Chemical Co., Ltd., which is an alicyclic epoxy compound, as a monomer Then, 1.0 part by weight of 1,4-bis (2-acryloyloxypropoxy) naphthalene synthesized by the method described in Example 3 was added and mixed uniformly to obtain a photocurable composition. This photocurable composition was applied to a surface of a polyester film (trade name: Lumirror, film thickness 100 μm) by a bar coater so as to have a film thickness of 12 μm. Then, a high pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was irradiated. The tack free time (curing time) until tackiness disappears was 2.5 minutes.

[Evaluation Test-9 as a Photopolymerization Sensitizer]
2 parts by weight of tolyl-i-butylphenyliodonium hexafluorophosphate (product name: Irgacure 250) manufactured by Dow Chemical Co., Ltd., which is an alicyclic epoxy compound as a monomer, manufactured by Dow Chemical Co. Part, 1.0 part by weight of 1,4-bis (2-acryloyloxybutoxy) naphthalene synthesized by the method described in Example 4 was added and mixed uniformly to obtain a photocurable composition. This photocurable composition was applied to a surface of a polyester film (trade name: Lumirror, film thickness 100 μm) by a bar coater so as to have a film thickness of 12 μm. Then, a high pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was irradiated. The tack free time (curing time) until tackiness disappears was 3 minutes.

[Evaluation Test-10 as a Photopolymerization Sensitizer]
2 parts by weight of tolyl-i-butylphenyliodonium hexafluorophosphate (product name: Irgacure 250) manufactured by Dow Chemical Co., Ltd., which is an alicyclic epoxy compound as a monomer, manufactured by Dow Chemical Co. 1,4-bis (2-acryloyloxy-3-butoxypropoxy) naphthalene (1.0 part by weight) synthesized by the method described in Example 5 was added to obtain a uniform photocurable composition. This photocurable composition was applied to a surface of a polyester film (trade name: Lumirror, film thickness 100 μm) by a bar coater so as to have a film thickness of 12 μm. Then, a high pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was irradiated. The tack free time (curing time) until tackiness disappears was 5 minutes.

[Evaluation Test as Photopolymerization Sensitizer-Comparative Example 1]
In the example described in Evaluation Test-1 as a photopolymerization sensitizer, a photocurable composition was prepared in exactly the same procedure as in the same example except that 1,4-bis (2-acryloyloxyethoxy) naphthalene was not added. The product was prepared, and the time until it was cured by irradiation with a high-pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was measured under a nitrogen atmosphere, but it did not cure even after 30 minutes. .

[Evaluation Test as Photopolymerization Sensitizer-Comparative Example 2]
In the example described in Evaluation Test-6 as a photopolymerization sensitizer, 1,4-bis (2-acryloyloxyetopoxy) naphthalene was not added, and photocuring was performed in exactly the same procedure as in the example. A composition was prepared, and the time until curing by irradiation with a high-pressure mercury lamp (irradiation intensity at 366 nm was 0.03 mw / cm ² ) was measured, but it did not cure even after 30 minutes. It was.

[Sublimation Test Example-1]
The polyester film coated with the photocurable composition prepared in the example described in Evaluation Test-3 as a photopolymerization sensitizer was heated in an oven adjusted to 180 ° C. A polyester film is taken out of the oven at regular intervals, and a UV absorbance peak at a wavelength of about 335 nm in a UV spectrum caused by 1,4-bis (2-acryloyloxypropoxy) naphthalene is measured with an ultraviolet / visible spectrophotometer ( Shimadzu Corporation model, UV: 2200). 1 and 2 show the UV spectra measured in this example. The absorbance peak height near the wavelength of 335 nm is compared between before heating (FIG. 1) and after heating (FIG. 2), and the rate of decrease in the absorbance peak after heating is examined to determine 1,4-bis (2-acryloyl). The degree of sublimation of oxypropoxy) naphthalene was determined. As a result, the peak height of the absorbance decreased by 5% after heating for 10 minutes, so it was determined that the temperature had sublimed by about 5%.

[Sublimation Test Example-2 (Comparative Example)]
In the example described in Evaluation Test-1 as a photopolymerization sensitizer, 1,4-diethoxynaphthalene was used instead of 1,4-bis (2-acryloyloxyethoxy) naphthalene. A polyester film coated with the photocurable composition and prepared in the same procedure was heated in an oven adjusted to 180 ° C. The polyester film is removed from the oven at regular intervals, the UV spectrum is measured (the measurement apparatus is the same as above), and the absorbance peak height near 1,335 nm of 1,4-diethoxynaphthalene is the same as in the above example. By examining, the degree of sublimation of the photocurable composition was determined. 3 and 4 show the UV spectra measured in this example. The absorbance peak height near the wavelength of 335 nm is compared between before heating (FIG. 3) and after heating (FIG. 4), and the decrease rate of the absorbance peak after heating is examined to sublimate 1,4-diethoxynaphthalene. The degree of was judged. As a result, it was found that 67% sublimated after 10 minutes.

  The 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound according to the first invention of the present invention is a novel compound, and this compound is a photocuring comprising a photopolymerizable monomer and a photopolymerization initiator. It can mix | blend with an adhesive composition and can utilize as a photoinitiator.

It is a UV spectrum of the sample before a heating in sublimation test example-1. It is a UV spectrum of the sample after a heating in sublimation test example-1. It is a UV spectrum of the sample before a heating in sublimation test example-2 (comparative example). It is a UV spectrum of the sample after a heating in sublimation test example-2 (comparative example).

Claims (7)

1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound represented by the structural formula (1).

{In Structural Formula (1), R _{1 and} R ₂ may be the same or different and each represents a hydrogen atom, an alkyl group, an aryl group, an alkoxymethyl group, an allyloxymethyl group, or an aryloxymethyl group, R _{3 and} R ₄ may be the same or different, each represents a hydrogen atom or a methyl group, X and Y may be the same or different, and a hydrogen atom, an alkyl group, a halogen atom, a hydroxyl group, an alkoxy group, an alkylthio group , An arylthio group, a carboxyl group, or a sulfonic acid group. } The 1,4-bis (2- (meth) acryloyloxy according to claim _1, wherein R _{1 and} R ₂ in the structural formula (1) are the same and are a methyl group, an ethyl group or an alkoxymethyl group. Alkoxy) naphthalene compounds.   1,4-dihydroxynaphthalene compound is reacted with alkylene oxide, glycidyl ether, or halogenated alcohol (halohydrin) to give 1,4-bis (2-hydroxyalkoxy) naphthalene compound, and then this compound is acryloyl chloride or chloride. The method for producing a 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound according to claim 1 or 2, wherein methacryloyl is reacted.   The method for producing a 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound according to claim 3, wherein the alkylene oxide is selected from ethylene oxide, propylene oxide or butylene oxide.   A photopolymerization sensitizer comprising the 1,4-bis (2- (meth) acryloyloxyalkoxy) naphthalene compound according to claim 1 or 2 as an active ingredient.   A photocurable composition comprising the photopolymerization sensitizer according to claim 5, a photopolymerization initiator, and a photopolymerizable monomer. The photocurable composition according to claim 6, wherein the photopolymerization initiator is an onium salt.

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