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MACROMONOMER, ITS SYNTHESIS AND GRAFT COPOLYMER PREPARED BY USING SAME

机译:相同单体制备的大分子单体及其合成和接枝共聚物

摘要

PURPOSE:To facilitate the control of the MW of the obtained macromonomer by polymerizing a monomer polymerizable by cationic living polymerization and reacting the formed polymer with a specified terminator to introduce a specified structure into the macromonomer. CONSTITUTION:A monomer (a) which can be polymerized by cationic living polymerization (e.g. 2-methyl-2-oxazoline) is subjected to cationic living polymerization, and the formed polymer is reacted with a terminator (b) which can terminate the polymerization by reaction with the cationic living terminals to obtain a macromonomer of formula I (wherein R1 is H, an alkyl or an aralkyl; A is a homo- or co-polymer of an MW of 50 to 100000 derived from an oxazoline compound, a 1,3-oxazoline compound, a cyclic imide compound, a tetrahydrofuran compound, an unsaturated ether compound, an aromatic vinyl compound, a carbazole compound or a sulfur-containing heterocyclic compound; X is a group of formula II or III or the like; Y is R2Y' or ArY'; R2 is formula IV; (m3) is 0 to 10; Ar is a group of formula V or VI or the like; Y' is -OH, -NH2 or the like; Z is R2Z' or ArZ'; R2 is a group of formula VII, (m4) is M3; and Z' is -H, -OH or the like).
机译:目的:通过聚合可通过阳离子活性聚合聚合的单体并使形成的聚合物与特定的终止剂反应,以将特定的结构引入大分子单体中,以方便控制所获得的大分子单体的分子量。组成:可以通过阳离子活性聚合(例如2-甲基-2-恶唑啉)聚合的单体(a)进行阳离子活性聚合,并使形成的聚合物与终止剂(b)反应,该终止剂可以通过以下方式终止聚合反应:与阳离子活性末端反应以获得式I的大分子单体(其中R1为H,烷基或芳烷基; A为由恶唑啉化合物衍生的MW为50至100000的均聚物或共聚物, 3-恶唑啉化合物,环状酰亚胺化合物,四氢呋喃化合物,不饱和醚化合物,芳族乙烯基化合物,咔唑化合物或含硫杂环化合物; X为式II或III等的基团; Y为R2Y′或ArY′; R2为式IV;(m3)为0至10; Ar为式V或VI等基团; Y′为-OH,-NH2等; Z为R2Z′或ArZ '; R2是式VII的基团,(m4)是M3;并且Z'是-H,-OH等。

著录项

  • 公开/公告号JPH02274712A

    专利类型

  • 公开/公告日1990-11-08

    原文格式PDF

  • 申请/专利权人 HOKUSHIN IND INC;KOBAYASHI SHIRO;

    申请/专利号JP19890096500

  • 申请日1989-04-18

  • 分类号C08G65/20;C08F26/12;C08F283/00;C08F290/00;C08F299/00;C08G65/16;C08G73/02;C08G73/04;C08G75/02;C08G75/06;

  • 国家 JP

  • 入库时间 2022-08-22 06:23:06

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