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Thomas E Gompf

from Penfield, NY
Deceased
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Also known as:
Thos E Gompf
Phone and address:
38 Thorntree Cir, Penfield, NY 14526
(585) 377-3579
Related to:
Josie Gompf, 24Amy C Vogt, 48
Connected to:
Erica J Gompper, 47Adolfo Gomringer, 59Barbara J Gomula, 71Betty Gon, 108Connie M Gon, 70Samuel M Gon, 105Sara M Gon, 59Kishan R Gona, 69Melissa A Gona, 62Surendra Gona, 53

Thomas Gompf Phones & Addresses

  • 38 Thorntree Cir, Penfield, NY 14526 (585) 377-3579
  • 1399 Monroe Ave, Rochester, NY 14618
  • 38 Thorntree Cir, Penfield, NY 14526 (585) 704-4131

Work

Position: Food Preparation and Serving Related Occupations

Education

Degree: Graduate or professional degree

Publications

Us Patents

Substituted Sulfonamido Compounds, Photosensitive Elements, Film Units, And Processes For Retaining A Photographic Image With Same

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US Patent:
42581206, Mar 24, 1981
Filed:
Apr 24, 1979
Appl. No.:
6/032972
Inventors:
Claude F. Gerbal - Bonneuil-sur-Marne, FR
Thomas E. Gompf - Rochester NY
Pierre D. Collet - Nogent-sur-Marne, FR
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
G03C 140
G03C 110
G03C 700
US Classification:
430223
Abstract:
A nondiffusible sulfonamido compound which is alkali-cleavable upon oxidation to release a diffusible photographically useful material, said nondiffusible sulfonamido compound having the formula: ##STR1## wherein: (a) R. sup. 1 is alkyl, aryl sulfamyl, carbamyl, carbonamido, carbonyl, carbonyloxy or sulfonamido; (b) R. sup. 2 is alkyl having from 1 to 18 carbon atoms, aryl, or alkylphenyl having from 7 to 12 carbon atoms; (c) R. sup. 3 and R. sup. 4 are independently alkyl, or aryl, or R. sup. 3 and R. sup. 4, taken together, form a fused carbocyclic or heterocyclic ring; (d) NHSO. sub. 2 PUG represents a sulfonamido group; (e) PUG represents a photographically useful group; and (f) at least one of R. sup. 1, R. sup. 2, R. sup. 3, or R. sup. 4, or any combination thereof, provides a molecular configuration of such size or shape as to render the compound nondiffusible under alkaline processing conditions, is useful as a redox releaser in photosensitive elements, photographic film units and in processes for transferring and/or retaining a photographic image in color diffusion transfer units. These elements, film units and processes produce retained color images having substantially reduced minimum densities.

Acetate Ester Compounds

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US Patent:
59591200, Sep 28, 1999
Filed:
Jun 12, 1997
Appl. No.:
8/873651
Inventors:
Jared B. Mooberry - Rochester NY
Thomas E. Gompf - Penfield NY
Brian H. Johnston - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07D24918
C07D40304
C07D40306
C07C32323
US Classification:
548253
Abstract:
The present invention provides an acetate ester compound of formula (III), ##STR1## a process for synthesizing compound (III), and a process for using that compound to prepare a pyrazolone compound, where the substituent definitions are as defined in the Summary of the Invention.

Substituted Sulfonamido Compounds, Photosensitive Elements, Film Units, And Processes For Retaining A Photographic Image With Same

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US Patent:
46056971, Aug 12, 1986
Filed:
Sep 16, 1983
Appl. No.:
6/533075
Inventors:
Claude F. Gerbal - Bonneuil-sur-Marne, FR
Thomas E. Gompf - Rochester NY
Pierre D. Collet - Nogent-sur-Marne, FR
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C09B 4300
C09B 4312
C09B 43124
C09B 43132
US Classification:
534648
Abstract:
A nondiffusible sulfonamido compound which is alkali-cleavable upon oxidation to release a diffusible photographically useful material, said nondiffusible sulfonamido compound having the formula: ##STR1## wherein: (a) R. sup. 1 is alkyl, aryl sulfamyl, carbamyl, carbonamido, carbonyl, carbonyloxy or sulfonamido; (b) R. sup. 2 is alkyl having from 1 to 18 carbon atoms, aryl, or alkylphenyl having from 7 to 12 carbon atoms; (c) R. sup. 3 and R. sup. 4 are independently alkyl, or aryl, or R. sup. 3 and R. sup. 4, taken together, form a fused carbocyclic or heterocyclic ring; (d) NHSO. sub. 2 PUG represents a sulfonamido group; (e) PUG represents a photographically useful group; and (f) at least one of R. sup. 1, R. sup. 2, R. sup. 3, or R. sup. 4, or any combination thereof, provides a molecular configuration of such size or shape as to render the compound nondiffusible under alkaline processing conditions, is useful as redox releaser in photosensitive elements, photographic film units and in processes for transferring and/or retaining a photographic image in color diffusion transfer units. These elements, film units and processes produce retained color images having substantially reduced minimum densities.

Photographic Products Employing Novel Nondiffusible Compounds Which Release Photographically Useful Groups

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US Patent:
46096108, Sep 2, 1986
Filed:
Aug 1, 1985
Appl. No.:
6/761280
Inventors:
Richard P. Dunlap - Penfield NY
Thomas E. Gompf - Penfield NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
G03C 140
G03C 554
G03C 108
G03C 134
US Classification:
430223
Abstract:
Photographic elements and assemblages are described which employ nondiffusible compounds which release photographically useful groups in an imagewise manner as the result of a. beta. -elimination reaction.

Silver Halide Color Photographic Element And Process Containing Leuco Dyes

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US Patent:
39389952, Feb 17, 1976
Filed:
Jul 10, 1974
Appl. No.:
5/487083
Inventors:
Thomas Edward Gompf - Penfield NY
William Henry Faul - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
G03C 700
G03C 140
US Classification:
96 55
Abstract:
Color photographic elements, compositions and processes for producing color negative images are described which employ a leuco dye comprising the reaction product of a color forming coupler and a N,N-dialkyl-p-phenylenediamine having an electronegative group attached to the benzene ring. The leuco dye is stable against aerial oxidation and can be developed to its corresponding dye with certain black and white developing compositions.

Silver Halide Emulsions With Incorporated 4,6-Difluorophenolic Couplers

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US Patent:
39986420, Dec 21, 1976
Filed:
Jul 11, 1975
Appl. No.:
5/594988
Inventors:
Philip T. S. Lau - Rochester NY
Roy L. Orvis - Rochester NY
Thomas E. Gompf - Penfield NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
G03C 140
US Classification:
96100
Abstract:
Color photographic elements are disclosed having, incorporated therein, one or more novel phenolic materials which have the following structure: ##STR1## wherein R. sub. 1 is a non-interfering alkyl, aryl, amino, substituted alkyl or substituted aryl ballasting group of the type which is useful in photographic incorporated cyan color-forming couplers, and R. sub. 2 is hydrogen or a lower alkyl group.

Blocked Pyrazolone Magenta Dye-Forming Couplers

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US Patent:
T110042, Sep 1, 1981
Filed:
Dec 29, 1980
Appl. No.:
6/220579
Inventors:
Thomas E. Gompf - Rochester NY
Howell A. Hammond - Rochester NY
Jared B. Mooberry - Rochester NY
International Classification:
C07D23110
US Classification:
548373
Abstract:
Novel 5-pyrazolone magenta dye-forming couplers are blocked with a coupler moiety which yields an alkali-soluble or colorless reaction product. The coupler moiety is joined via its coupling position to the enol oxygen of the 5-pyrazolone and is displaced therefrom during processing as a result of reaction by means of oxidized color developing agent to thereby activate the 5-pyrazolone coupler. These couplers have good reactivity and good resistance to aerial contaminants, such as formaldehyde, and can be incorporated in photographic emulsions and elements.

Silver Halide Elements Containing Blocked Pyrazolone Magenta Dye-Forming Couplers

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US Patent:
42834724, Aug 11, 1981
Filed:
Feb 26, 1980
Appl. No.:
6/124872
Inventors:
Thomas E. Gompf - Rochester NY
Howell A. Hammond - Rochester NY
Jared B. Mooberry - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
G03C 700
US Classification:
430 17
Abstract:
Novel 5-pyrazolone magenta dye-forming couplers are blocked with a coupler moiety which yields an alkali-soluble or colorless reaction product. The coupler moiety is joined via its coupling position to the enol oxygen of the 5-pyrazolone and is displaced therefrom during processing as a result of reaction by means of oxidized color developing agent to thereby activate the 5-pyrazolone coupler. These couplers have good reactivity and good resistance to aerial contaminants, such a formaldehyde, and can be incorporated in photographic emulsions and elements.
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Thomas E Gompf from Penfield, NYDeceased Get Report