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Block copolymer, method for producing same, and film

A technology of block copolymers and segments, which is applied in the field of block copolymers and its manufacture, can solve the problems of unstable introduction rate, loss of transparency, lack of practicability of blocks, etc., and achieve excellent transparency and high-efficiency transparency sexual effect

Active Publication Date: 2019-01-18
JSR CORPORATIOON
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] However, it is difficult to separate from the homopolymer, so purification must be repeated many times, which becomes a high cost
Furthermore, the incorporation rate of styrenes is not stable, and there is a problem in quality, so it is not a method that can be mass-produced
In addition, the obtained block body also lacks practicality. For example, in the case of stretching operations that are often performed on optical films, there is a problem of whitening and loss of transparency.

Method used

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  • Block copolymer, method for producing same, and film
  • Block copolymer, method for producing same, and film
  • Block copolymer, method for producing same, and film

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0270] 35 parts of the macromonomer (A), 65 parts of the following compound (m-1) (8-methyl-8-methoxycarbonyl-tetracyclo[4.4.0.1 2,5 .1 7,10 ] dode-3-ene), and 150 parts of toluene are mixed in the autoclave, the inner temperature is heated to 100°C, and 0.00116 parts of the metathesis polymerization catalyst ([1,3-bis(2 , 4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro[[2-(1-methylacetoxy)phenyl]methylene]ruthenium(II)), stirred for 1 hour . Next, 0.00025 parts of ethyl vinyl ether was added to stop the reaction.

[0271] [Compound (m-1)]

[0272] [chemical 14]

[0273]

[0274] [Metathesis Polymerization Catalyst]

[0275] [chemical 15]

[0276]

[0277] Then, 110 parts of toluene, 20 ppm of the hydrogenation reaction catalyst (Ru[4-CH 3 (CH 2 ) 4 C 6 h 4 CO 2 ]H(CO)[P(C 6 h 5 ) 3 ] 2 ), pressurized to 10 MPa of hydrogen at 165° C., and stirred for 3 hours to carry out hydrogenation reaction.

[0278] Next, the reaction solution was added dropwise ...

Embodiment 2

[0287] 35 parts of the macromonomer (B), 65 parts of the compound (m-1) (8-methyl-8-methoxycarbonyl-tetracyclo[4.4.0.1 2,5 .1 7,10 ] dodec-3-ene), and 150 parts of toluene are mixed in the autoclave, the inner temperature is heated to 100°C, and 0.00116 parts of the metathesis polymerization catalyst ([1,3-bis(2,4 , 6-trimethylphenyl)-2-imidazolidinylidene]dichloro[[2-(1-methylacetoxy)phenyl]methylene]ruthenium(II)), stirred for 1 hour. Next, 0.00025 parts of ethyl vinyl ether was added to stop the reaction.

[0288] Then, the hydrogenation catalyst (Ru[4-CH 3 (CH 2 ) 4 C 6 h 4 CO 2 ]H(CO)[P(C 6 h 5 ) 3 ] 2 ), pressurized to 10 MPa of hydrogen at 165° C., and stirred for 3 hours to carry out hydrogenation reaction.

[0289] Next, the reaction solution was added dropwise to 3000 parts of methanol, and the obtained precipitate was collected, filtered and dried to obtain 96 parts of the block copolymer of Example 2 having the following structure.

[0290] In addition...

Embodiment 3

[0296] 30 parts of the macromonomer (B), 70 parts of the compound (m-1) (8-methyl-8-methoxycarbonyl-tetracyclo[4.4.0.1 2,5 .1 7,10 ] dodec-3-ene), and 150 parts of toluene are mixed in the autoclave, the inner temperature is heated to 100°C, and 0.00116 parts of the metathesis polymerization catalyst ([1,3-bis(2,4 , 6-trimethylphenyl)-2-imidazolidinylidene]dichloro[[2-(1-methylacetoxy)phenyl]methylene]ruthenium(II)), stirred for 1 hour. Next, 0.00025 parts of ethyl vinyl ether was added to stop the reaction.

[0297] Then, the hydrogenation catalyst (Ru[4-CH 3 (CH 2 ) 4 C6 h 4 CO 2 ]H(CO)[P(C 6 h 5 ) 3 ] 2 ), pressurized to 10 MPa of hydrogen at 165° C., and stirred for 3 hours to carry out hydrogenation reaction.

[0298] Next, the reaction liquid was added dropwise to 3000 parts of methanol, and the obtained precipitate was collected, filtered and dried to obtain 96 parts of the block copolymer of Example 3 having the following structure.

[0299] In addition, th...

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Abstract

The invention provides a block copolymer and a preparation method thereof and a membrane, wherein the block copolymer is high in transparency and useful in the optical field. The block copolymers of the present invention comprises a block part (A) containing a structure unit represented by the following formula (1), and a block part (B) containing a structure unit represented by the following formula (2). In addition, R1 and R2 represent a hydrogen atom or methyl; R3 and R4 represents a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a hydroxyl group, an alkyl group, a cycloalkyl group, an alkyl ester or alkoxy group; X represents a methylene, an oxygen atom or a sulfur atom; A1-A4 represent particular groups, atoms or the like; p is an integer of 0-3; q is an integer of 0-4; r is 0 or 1; m is an integer of 0-3; n is 0 or a positive integer.

Description

technical field [0001] The present invention relates to a block copolymer, its production method and film. More specifically, the present invention relates to a highly transparent block copolymer useful in the optical field, a method for producing the same, and a film comprising the block copolymer. Background technique [0002] Cyclic olefin-based resins such as thermoplastic norbornene-based resins have high glass transition temperature, high light transmittance, and small anisotropy of refractive index, so they have low birefringence compared with conventional optical films. specialty. Therefore, it has attracted attention as a transparent thermoplastic resin excellent in heat resistance, transparency, and optical characteristics. Further studies are being made to apply cyclic olefin-based resins to optical fields such as optical materials such as optical discs, optical lenses, optical fibers, and transparent plastic substrates, sealing materials such as optical semicon...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08F293/00C08L53/00
Inventor 江畑琢磨寺岛勇辉山本达之中村和洋铃木义信安藤嘉彦
Owner JSR CORPORATIOON