Larry D. Edwards - Rochester NY Frederick J. Sauter - Rochester NY George J. Burgmaier - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
G03C 102
US Classification:
430353
Abstract:
Photographic silver halide is spectrally sensitized by means of at least one bleachable spectral sensitizing dye comprising a cyanine dye nucleus and a particular N-methylene substituent. The spectrally sensitized photographic silver halide is useful in a photothermographic material. An image in the photothermographic material, after exposure, is developed and the spectral sensitizing dye is bleached, especially at elevated pH, by heating the photothermographic material to processing temperature.
Wolfgang H. H. Gunther - West Chester PA Frederick J. Sauter - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07D41706
US Classification:
544300
Abstract:
A merocyanine dye having the formula: ##STR1## wherein: R. sub. 1 and R. sub. 2 independently are H, alkyl, alkoxy or aryl
R. sub. 7 and R. sub. 8 are H or
any of R. sub. 1 and R. sub. 2, R. sub. 1 and R. sub. 7, R. sub. 2 and R. sub. 8 can together comprise the atoms necessary to form a fused aromatic ring on the benzene radical to which they are attached;
R. sub. 5 and R. sub. 6 comprise alkyl of from 1-18 carbon atoms provided that the sum of the carbon atoms in R. sub. 5 and R. sub. 6 is at least 8;
R. sub. 9 is an alkylene group of 2-9 nuclear carbon and hetero atoms; and
Z. sup. + is a cation.
This dye is useful in a method for inactivating viruses comprising contacting the viruses with the compound and exposing the resulting mixture to visible light to excite and inactivate the viruses. The compounds are also useful in the irradiation-induced inactivation of leukemia cells.
Wolfgang H. H. Gunther - West Chester PA Frederick J. Sauter - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07D42106
US Classification:
544300
Abstract:
A merocyanine dye having the formula: ##STR1## wherein: R. sub. 1 and R. sub. 2 independently are H, alkyl, alkoxy or aryl,
R. sub. 7 and R. sub. 8 are H or any of R. sub. 1 and R. sub. 2, R. sub. 1 and R. sub. 7, R. sub. 2 and R. sub. 8 can together comprise the atoms necessary to form a fused aromatic ring on the benzene radical to which they are attached;
R. sub. 5 and R. sub. 6 comprise alkyl of from 1-18 carbon atoms provided that the sum of the carbon atoms in R. sub. 5 and R. sub. 6 is at least 8;
R. sub. 9 is an alkylene group of 2-9 nuclear carbon and hetero atoms; and
Z. sup. + is a cation.
This dye is useful in a method for inactivating viruses comprising contacting the viruses with the compound and exposing the resulting mixture to visible light to excite and inactivate the viruses. The compounds are also useful in the irradiation-induced inactivation of leukemia cells.
Wolfgang H. H. Gunther - West Chester PA Frederick J. Sauter - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07D40506 C07D40906 G03G 506
US Classification:
544300
Abstract:
A merocyanine dye having the formula: ##STR1## wherein: R. sub. 1 and R. sub. 2 independently are H, alkyl, alkoxy or aryl; R. sub. 7 and R. sub. 8 are H or
any of R. sub. 1 and R. sub. 2, R. sub. 1 and R. sub. 7, and R. sub. 2 and R. sub. 8 can together comprise the atoms necessary to form a fused aromatic ring on the benzene radical to which they are attached and with the stipulation that only one of R. sub. 1 and R. sub. 2 can be H;
R. sub. 5 and R. sub. 6 comprise alkyl of from 1-18 carbon atoms, provided that the sum of the carbon atoms in R. sub. 5 and R. sub. 6 together is at least 8;
R. sub. 9 is an alkylene group of 2-9 nuclear carbon and hetero atoms; and
Z. sup. + is a cation.
This dye is useful in a method for inactivating viruses comprising contacting the viruses with the compound and exposing the resulting mixture to visible light to excite and inactivate the viruses.
Amide Substituted Dye Compounds And Silver Halide Photographic Elements Containing Such Dyes
Richard L. Parton - Webster NY David A. Stegman - Churchville NY Frederick J. Sauter - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
G03C 1035 G03C 114
US Classification:
430567
Abstract:
Dyes and photographic elements containing them as silver halide sensitizing dyes, which dyes have the structure: ##STR1## wherein: X1 and X2 each independently represent the atoms necessary to complete a benzo-condensed 5- or 6-membered heterocyclic nucleus, which, in addition to being substituted by Z1 and Z2 respectively, may be further substituted or unsubstituted;
n is a positive integer from 1 to 4,
p and q each independently represents 0 or 1,
each L independently represents a substituted or unsubstituted methine group,
R1 and R2 each independently represents substituted or unsubstituted aryl or substituted or unsubstituted alkyl,
Z1 represents a substituent which contains both an amide group and an aromatic ring which may be appended or fused to X1; and
W1 is a counterion as needed to balance the charge of the molecule.
Wolfgang H. Gunther - West Chester PA Frederick J. Sauter - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07D41706
US Classification:
544300
Abstract:
A merocyanine dye having the formula: ##STR1## wherein: R. sup. 1 and R. sup. 2 independently are H, alkyl, alkoxy, or aryl, and
R. sup. 7 and R. sup. 8 may each be H with the proviso that a pair of R's selected from the pairs R. sup. 1 and R. sup. 2, R. sup. 1 and R. sup. 7, and R. sup. 2 and R. sup. 8 can together comprise the atoms necessary to form a fused aromatic ring on the benzene radical to which they are attached and only one of R. sup. 1 and R. sup. 2 can be H;
R. sup. 5 and R. sup. 6 comprise alkyl of from 1-18 carbon atoms provided that the sum of the carbon atoms in R. sup. 5 and R. sup. 6 is at least 8;
R. sub. 9 is an alkylene group of 2-9 nuclear carbon and hetero atoms; and
Z. sup. + is a cation.
This dye is useful in a method for inactivating viruses comprising contacting the viruses with the compound and exposing the resulting mixture to visible light to excite and inactivate the viruses.