U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Novel polyimides, and polyamic acid and ester intermediates thereof

Patent 4405770 Issued on September 20, 1983. Estimated Expiration Date: Icon_subject August 12, 2001. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

3505288

3609123

3793291

Novel nitrogen-containing aromatic polymers and process for their preparation
Patent #: 4086209
Issued on: 04/25/1978
Inventor: Hara, et al.

Aromatic diamines and their use as polycondensation components for the manufacture of polyamide, polyamide-imide and polyimide polymers
Patent #: 4239880
Issued on: 12/16/1980
Inventor: Darms

Novel vinyl end-capped polyimide oligomers
Patent #: 4251419
Issued on: 02/17/1981
Inventor: Heilman ,   et al.

Acetylene terminated imide oligomers which melt at low temperatures
Patent #: 4276407
Issued on: 06/30/1981
Inventor: Bilow ,   et al.

Methods of preparing polyimides and polyimide precursors Patent #: 4296208
Issued on: 10/20/1981
Inventor: Gagliani ,   et al.

Inventors

Assignee

Application

No. 06/292257 filed on 08/12/1981

US Classes:

526/259, Nitrogen atom is part of a bridged or fused ring system428/473.5, Of polyimide526/262, Imide monomer526/270, 5-membered heterocyclic ring compound contains at least one oxygen atom526/271, Acid anhydride526/285, From monomer containing an acetylenic group526/304, Contains oxygen atom other than in amide form bonded to a carbon atom526/305, Cycloaliphatic or aromatic526/306, Plural amide group containing528/125, From ketone-containing phenolic reactant or with ketone-containing reactant528/126, Polymerizing in the presence of a specified material other than reactant528/128, With nonphenolic or nonketone reactant528/172, Nitrogen-containing compound is a reactant other than wherein nitrogen is solely present as a carboxylic acid derivative528/179, Polymerizing in the presence of a specified material other than a reactant and other than Group IA or Group IIA material as sole metal atom528/182, Material is a nitrogen-containing compound528/185, Phenolic reactant contains at least two aryl rings and two diverse phenolic to oxygen bonds528/188, Reactant contains three or more carboxylic acid groups or is derivative thereof528/220, FROM KETONE OR KETENE REACTANT528/222, Polymerizing in the presence of a specified material other than a reactant528/224, Material contains a nitrogen-containing compound528/229, Nitrogen-containing reactant contains an amine group528/352, Phosphorus- or sulfur-containing reactant528/353, Carboxylic acid contains at least four carboxylic acid groups or is a derivative of a carboxylic acid containing at least four carboxylic groups564/305Benzene ring containing

Examiners

Primary: Lee, Lester L.

Attorney, Agent or Firm

International Classes

C08G 73/10 (20060101)
C08G 73/00 (20060101)

Abstract

Novel polyimides, optionally end-capped with polymerizable or inert groups, and the polyamic acid or ester intermediates thereof are prepared by reacting a tetracarboxylic acid compound (e.g. pyromellitic dianhydride or 3,3',4,4'-benzophenone tetracarboxylic acid dianhydride or its methyl diester) with diamines having the general formula ##STR1## wherein Z is oxygen or sulfur, X and/or Y are carbonyl or carbinol groups, the amine groups may be in the 2-, 3-, and/or 4-position, and isomerism is present when X and/or Y is a carbinol group. The polyimides may be end-capped by reaction, during or after their formation, with polymerizable groups such as 3-aminophenyl acetylene or 3,6-endomethylene-1,2,3,6-tetrahydrophthalic anhydride. The diamines are novel classes of amines when Z is sulfur and when Z is oxygen and X, Y, or X and Y are carbinol groups.

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