The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Sep. 24, 1985

Filed:

Apr. 18, 1983
Applicant:
Inventor:

Lee Traynor, Akron, OH (US);

Assignee:

The B. F. Goodrich Company, Akron, OH (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C08D / ; C08F / ;
U.S. Cl.
CPC ...
526258 ; 2041802 ; 252500 ; 548400 ; 548517 ; 548518 ; 548541 ; 548577 ; 548579 ;
Abstract

Organic polymers which are 'hydroxyphenyl-substituted' and 'ether-substituted' polypyrroles ('PP') linked through N-adjacent C atoms, are disclosed which are compactable, extrudable and are also electrical conductors. When such PPs are prepared by electrochemical deposition with an appropriate electrolyte, they are also soluble in commonly available solvents, provided at least one of the 3- or 4- positions of the pyrrole nucleus is substituted with a substituent having either a hydroxyphenyl, or an ether structure. By choice of the hydroxyphenyl and/or ether substituent on one of the substitutable positions (3- or 4-) of the pyrrole nucleus, or both, the PP may be tailored for use either as a semiconductor having a conductivity in the range from about 10.sup.-5 to about 10.sup.-2 S/cm, or a relatively good conductor having a conductivity in the range from about 10.sup.-2 to about 10.sup.2 S/cm. A method is disclosed for preparing an ether-substituted pyrrole comprising reacting a non-Michael acceptor selected from the group consisting of esters, ketones and nitriles having vinylene carbon atoms, with tosylmethylisocyanide, in the presence of a solvent, so as to form a hydroxyphenyl-substituted or an ether-substituted pyrrole directly without substituting the pyrrole ring in the 2- and 5- positions.


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