Polyimide having an alcoholic hydroxyl group and a process for the preparation thereof
Abstract
This invention relates to a novel polyimide silicone having an alcoholic hydroxyl group and a process for the preparation thereof. The polyimide of the invention having a primary alcoholic hydroxyl group is represented by the following general formula (1), wherein X represents a tetravalent organic group, Y represents a divalent group having at least one monovalent group selected from the group consisting of a phenolic hydroxyl group and a carboxyl group, with at least one being a divalent organic group having an alcoholic hydroxyl group, Z represents a divalent organic group, W represents a divalent organic group having an organosiloxane structure, k is a positive number, and each of m and n is equal to 0 (zero) or a positive number, with 0.1≦k/(k+m+n)≦1, 0≦m/(k+m+n)≦0.8, 0≦n/(k+m+n)≦0.8.
Claims
exact text as granted — not AI-modified1 . Polyimide having a primary alcoholic hydroxyl group and represented by the following general formula (1),
wherein
X represents a tetravalent organic group,
Y represents a divalent organic group represented by the general formula (2),
wherein
A may be same with or different from one another and represents a divalent organic group selected from the following radicals:
each of B and C may be same with or different from one another and represents a hydrogen atom or an alkyl group having from 1 to 4 carbon atoms, each of a and b is 0 or 1,
c is an integer of from 0 to 10, and
R 1 may be the same with or different from one another and is a monovalent group selected from the group consisting of a phenolic hydroxyl group, a carboxyl group, and an organic group having an alcoholic hydroxyl group, with at least one R 1 being an organic group having a primary alcoholic hydroxyl group,
Z represents a divalent organic group,
W represents a divalent organic group having an organosiloxane structure,
k is a positive number, and
each of m and n is equal to 0 (zero) or a positive number, with 0.1.k/(k+m+n).1, 0.m/(k+m+n).0.8, 0.n/(k+m+n).0.8.
2 . The polyimide having an alcoholic hydroxyl group according to claim 1 , wherein R 1 in said general formula (2) is a monovalent group selected from the group consisting of —OH, —COON, —OCH 2 CH(OH)CH 2 OH, —OCH(CH 2 OH)CH 2 OH, —COOCH 2 CH(OH)CH 2 OH, and —COOCH(CH 2 OH)CH 2 OH.
3 . The polyimide having an alcoholic hydroxyl group according to claim 1 , wherein X in said general formula (1) is a tetravalent organic group represented by any one of the following formulas,
4 . The polyimide comprising an alcoholic hydroxyl group according to claim 1 , wherein Z in said general formula (1) is a divalent organic group represented by the following general formula (3),
wherein D may be same with or different and is a divalent organic group selected from the following radicals;
and each of e, f, and g is 0 or 1.
5 . The polyimide comprising an alcoholic hydroxyl group according to claim 1 , wherein W in said general formula (1) is a divalent organic group represented by the following general formula (4),
wherein R 3 may be same with or different and is a monovalent hydrocarbon group having from 1 to 8 carbon atoms and h is a positive number of from 1 to so.
6 . The siloxane-modified polyimide comprising an alcoholic hydroxyl group according to claim 1 , wherein 3≦n≦400.
7 . A process for the preparation of a polyimide having an alcoholic hydroxyl group represented by the general formula (1), wherein an acid dianhydride is reacted with a diamine having at least one selected from a phenolic hydroxyl group and a carboxyl group, optionally a diamine having neither a phenolic hydroxyl group nor a carboxyl group, and also optionally a diaminosilicone, to obtain a polyamic acid, subsequently the resulting polyamic acid is subjected to dehydration cyclization to obtain a polyimide having at least one selected from a phenolic hydroxyl group and a carboxyl group and represented by the general formula (5),
wherein, X, Z, W, k, m, and n are as defined above, and Y′ is a divalent organic group represented by the general formula (6),
wherein A, 3, C, a, b, and c are as defined above, and R 2 is —OH or —COOH,
and then the polyimide is reacted with a glycidol at a temperature of from 40 to 180° C.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.