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Process for making photopolymerizable aromatic polyamic acid derivatives

Assignee: EIDP Inc
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Filing: 1985-04-26
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Granted: 1985-11-05
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Expires: 2005-04-26
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Abstract

Abstract A process for the synthesis of the photosensitive polyamic acid derivatives which are polyimide precursors, comprising the sequential steps: (1) Partially derivatizing an aromatic dianhydride with a reactive monomer containing a photosensitive moiety; (2) Condensation polymerizing the partially derivatized aromatic dianhydride with aromatic diamine to form polyamic acid; (3) Isoimidization of the polyamic acid; (4) Condensation of the polyisoimide to polyamic acid derivative by reaction with additional reactive monomer; and (5) Separation of the polyamic acid derivative.

Inventors

  • 👤 Michael Fryd
  • 👤 David L. Goff

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 19:07
CPC Classifications
C; C08; C08G; C08G73/00; C08G73/06; C08G73/10; C08G73/12; C08G73/1003; C08G73/1007; C08G73/1028; C08G73/1025; C08G73/1057; C08G73/1064; C08G73/1067; C08G73/1071; C08G73/1085; C08G73/1089; G; G03; G03F; G03F7/00; G03F7/004; G03F7/038; G03F7/0387

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 250 words
A process for the synthesis of photosensitive polyamicacid derivatives which are polyimide precursors comprising the sequential steps: (1) forming a solution in aprotic solvent of aromatic dianhydride and monomer(s) corresponding to the formula RZH, wherein R is an ethylenically unsaturated moiety capable of addition polymerization and Z is --O--, --S-- or --NR'-- wherein R' is --H or C 1-4 alkyl, the amount of monomer being 0-40 equivalent %, basis dianhydride, and maintaining the solution for a time and temperature sufficient to effect partial reaction of the aromatic dianhydride with substantially all of the monomer; (2) admixing with and dissolving in the aromatic dianhydride-containing reaction solution of step (1) aromatic diamine while maintaining the reaction solution below 50° C. to effect condensation polymerization of the unreacted anhydride and the amine moieties to form the corresponding polyamic acid(s); (3) admixing with and dissolving in the polyamic acid(s)-containing reaction solution of step (2) an isoimidization agent selected from the group consisting of N,N'-dihydrocarbyl-substituted carbodiimides, trifluoroacetic acid anhydride and mixtures thereof to convert the polyamic acid(s) to the corresponding polyisoimide(s); (4) admixing with and dissolving in an aprotic solution of the polyisoimide(s) of step (3) a molar excess of monomer corresponding to the formula RZH and maintaining the solution for a time and temperature sufficient to effect substantially complete esterification of the carboxylic acid moieties of the polyisoimide(s) with monomer and converting the polyisoimide(s) to the corresponding polyamic acid derivatives; and (5) separation of polyamic acid derivatives from the reaction solution of step (4).
Claim 2
Dependent Claim 250 words
A process for the synthesis of photosensitive polyamicacid derivatives which are polyimide precursors comprising the sequential steps: (1) forming a solution in aprotic solvent of aromatic dianhydride and monomer(s) corresponding to the formula RZH, wherein R is an ethylenically unsaturated moiety capable of addition polymerization and Z is --O--, --S-- or --NR'-- wherein R' is --H or C 1-4 alkyl, the amount of monomer being 0-40 equivalent %, basis dianhydride, and maintaining the solution for a time and temperature sufficient to effect partial reaction of the aromatic dianhydride with substantially all of the monomer; (2) admixing with and dissolving in the aromatic dianhydride-containing reaction solution of step (1) aromatic diamine while maintaining the reaction solution below 50° C. to effect condensation polymerization of the unreacted anhydride and the amine moieties to form the corresponding polyamic acid(s); (3) admixing with and dissolving in the polyamic acid(s)-containing reaction solution of step (2) an isoimidization agent selected from the group consisting of N,N'-dihydrocarbyl-substituted carbodiimides, trifluoroacetic acid anhydride and mixtures thereof to convert the polyamic acid(s) to the corresponding polyisoimide(s); (4) admixing with and dissolving in an aprotic solution of the polyisoimide(s) of step (3) a molar excess of monomer corresponding to the formula RZH and maintaining the solution for a time and temperature sufficient to effect substantially complete esterification of the carboxylic acid moieties of the polyisoimide(s) with monomer and converting the polyisoimide(s) to the corresponding polyamic acid derivatives; and (5) separation of polyamic acid derivatives from the reaction solution of step (4).

References Cited (Backward Citations)

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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-11-04 1989-05-06 1989-11-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-11-04 1993-05-06 1993-11-05 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-11-04 1997-05-06 1997-11-05 $7700.00 Window Closed / Lapsed

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