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Lee Leora A Traynor, 861705 Hillsboro Ave SE, Grand Rapids, MI 49546

Lee Traynor Phones & Addresses

Grand Rapids, MI   

Ada, MI   

Adrian, MI   

2824 Yellow Creek Rd, Akron, OH 44333    330-8646375   

Medina, OH   

Wadsworth, OH   

2824 Yellow Creek Rd, Akron, OH 44333    330-3107099   

Work

Position: Food Preparation and Serving Related Occupations

Education

Degree: Bachelor's degree or higher

Mentions for Lee Leora A Traynor

Publications & IP owners

Us Patents

Polymethylene Pyrroles And Electrically Conductive Polymers Thereof

US Patent:
4487667, Dec 11, 1984
Filed:
May 16, 1983
Appl. No.:
6/494752
Inventors:
Lee Traynor - Akron OH
Assignee:
The B. F. Goodrich Company - Akron OH
International Classification:
C25B 100
US Classification:
204 59R
Abstract:
Cycloalk-2-enes and cycloalk-2-ene-dienes are found to be Michael acceptors which react with tosylmethylisocyanide to form bicyclo fused-ring compounds. A wide variety of substituents may be introduced on the alkylene ring with the aid of the carbonyl group(s) on the fused-ring compound. These carbonyl-containing bicyclo fused-ring compounds may be reduced to provide monomers which may be electrodeposited as substituted polypyrroles ("PP") which are electrically conductive, compactable and extrudable organic polymers. By choice of substituents on the alkylene ring which bridges the 3- and 4- carbon atoms of the pyrrole ring, 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.

Polymethylene Pyrroles

US Patent:
4602090, Jul 22, 1986
Filed:
Dec 10, 1984
Appl. No.:
6/679846
Inventors:
Lee Traynor - Akron OH
Assignee:
The B. F. Goodrich Company - Akron OH
International Classification:
C07D40106
C07D20952
US Classification:
546272
Abstract:
Cycloalk-2-enes and cycloalk-2-ene-dienes are found to be Michael acceptors which react with tosylmethylisocyanide to form bicyclo fused-ring compounds. A wide variety of substituents may be introduced on the alkylene ring with the aid of the carbonyl group(s) on the fused-ring compound. These carbonyl-containing bicyclo fused-ring compounds may be reduced to provide monomers which may be electrodeposited as substituted polypyrroles ("PP") which are electrically conductive, compactable and extrudable organic polymers. By choice of substituents on the alkylene ring which bridges the 3- and 4-carbon atoms of the pyrrole ring, 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.

Non-Catalytic Process For The Preparation Of Difunctionalized Polyarylene Polyethers

US Patent:
4663402, May 5, 1987
Filed:
Dec 30, 1985
Appl. No.:
6/814749
Inventors:
Virgil Percec - Pepper Pike OH
Gary S. Huvard - Akron OH
Floyd L. Ramp - Richfield OH
Lee Traynor - Akron OH
Assignee:
The B. F. Goodrich Company - Akron OH
International Classification:
C08G 6548
C08G 7523
US Classification:
525534
Abstract:
A non-catalytic process converts oligomers of polyarylene polyethers (PAPE) having a mol wt Mn in the range from 1000 to about 10,000 to difunctionalized oligomers so as, in the first instance, to provide a reactive double bond (for example, a vinylbenzyl group) at each end of the PAPE; and, in the second instance to provide a triple bond (benzylethynyl group) at each end of the PAPE. The solubility of intermediate bisphenolates of (i) a dihydric phenol, and of (ii) the PAPE oligomer in particular solvents which allow (a) water of reaction to be removed without being degraded, and (b) essentially complete end-capping of the oligomer chains with vinyl chain ends, are the keys to the novel process. The PAPE most preferably has a repeating unit which is the residuum of two dihydric phenols or thiophenols ("DHP") linked through a C. dbd. O, --S--S--, or --SO. sub.

Electrically Conductive Pyrrole Polymers

US Patent:
4543402, Sep 24, 1985
Filed:
Apr 18, 1983
Appl. No.:
6/486161
Inventors:
Lee Traynor - Akron OH
Assignee:
The B. F. Goodrich Company - Akron OH
International Classification:
C08D 1300
C08F12606
US Classification:
526258
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.

Electrically Conductive Pyrrole Polymers And Process Of Preparing The Same

US Patent:
4629798, Dec 16, 1986
Filed:
Aug 19, 1985
Appl. No.:
6/767209
Inventors:
Lee Traynor - Akron OH
Assignee:
The B. F. Goodrich Company - Akron OH
International Classification:
C07D20730
C07D40112
US Classification:
548562
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.

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