Cyclopropenone vesicular imaging composition, element and process

Claim 2

In a vesicular imaging composition comprising: (I) a polymeric binder having sufficient gas impermeability as to provide a latent image stability period for CO that is substantially greater than about one minute when ascertained for an element having a dried binder thickness of between about 10 and about 15 microns; and (II) admixed with said binder, a radiation-decomposable vesiculating agent capable of generating a gas upon imagewise exposure; the improvement wherein the vesiculating agent is a cyclopropenone having a λ max in ethanol no greater than about 400 nm in the spectral range of about 250 to about 650 nm.

Claim 3

A composition as defined in claim 1 wherein said cyclopropenone has the formula: ##STR7## wherein: R 1 and R 2 are the same or different, and are each a substituted or unsubstituted aryl radical containing from 6 to 10 carbon atoms in the aromatic ring, or an aralkenyl radical having 6 to 10 carbon atoms in the aryl portion and 1 to 5 carbon atoms in the alkenyl portion; the substituents of each of said substituted aryl radical being one or more radicals selected from the group consisting of: (1) alkyl or alkoxy containing from 1 to 5 carbon atoms; (2) nitro; (3) aryloxy containing from 6 to 10 carbon atoms; (4) halogen; and (5) a polymer to which the aryl radical is attached as a dependent moiety, the polymer having at least one repeating unit which is a lower alkylene containing from 1 to 5 carbon atoms.

Claim 4

A composition as defined in claim 2 wherein at least one of R 1 and R 2 is a bi-substituted aryl radical.

Claim 5

A composition as defined in claim 3 wherein said agent is 2-(4-methoxyphenyl)-3-phenylcyclopropenone.

Claim 6

A composition as defined in claim 1 wherein said agent is diphenylcyclopropenone.

Claim 7

A composition as defined in claim 1 and further including a spectral sensitizing compound having a λ max in methanol which is less than about 450 nm, said compound being one that, when co-dissolved with a sulfonamide polymer and an amount of said cyclopropenone effective to photogenerate an image, forms a composition which can be dried in a layer and which upon imagewise exposure demonstrates a spectral response at a wavelength that is (a) longer than the limit of the spectral sensitivity of the cyclopropenone and (b) still within the absorbence region of said compound.

Claim 8

A composition as defined in claim 6, wherein said compound is 2-benzoylmethylene-3-methylnaphtho(2,1-a) thiazoline.

Claim 9

A composition as defined in claim 6, wherein said compound is 3-carboxymethyl-5-(3-ethylbenzothiazolinylidene)rhodanine.

Claim 10

A composition as defined in claim 6, wherein said compound is anhydro-3,3'-disulfopropyl-5-methoxythiacyanine hydroxide.

Claim 11

A vesicular imaging element, comprising: a support; coated on the support, a water-insoluble, thermoplastic binder having a gas impermeability sufficient to provide a latent image stability period for CO that is substantially greater than about one minute when ascertained for an element having a dried binder thickness of between about 10 and about 15 microns; as a vesiculating agent, a cyclopropenone admixed with said binder, having the formula: ##STR8## wherein: R 1 and R 2 are the same or different, and are each a substituted or unsubstituted aryl radical containing from 6 to 10 carbon atoms in the aromatic ring, or an aralkenyl radical having 6 to 10 carbon atoms in the aryl portion and 1 to 5 carbon atoms in the alkenyl portion; the substituents of each of said substituted aryl radical being one or more radicals selected from the group consisting of: (1) alkyl or alkoxy containing from 1 to 5 carbon atoms; (2) nitro; (3) aryloxy containing from 6 to 10 carbon atoms; (4) halogen; and (5) a polymer to which the aryl radical is attached as a dependent moiety, the polymer having at least one repeating unit which is a lower alkylene containing from 1 to 5 carbon atoms.

Claim 12

A vesicular imaging element, comprising: a support; coated on the support, a water-insoluble, thermoplastic binder having a gas impermeability sufficient to provide a latent image stability period for CO that is substantially greater than about one minute when ascertained for an element having a dried binder thickness of between about 10 and about 15 microns; as a vesiculating agent, a cyclopropenone admixed with said binder, having the formula: ##STR8## wherein: R 1 and R 2 are the same or different, and are each a substituted or unsubstituted aryl radical containing from 6 to 10 carbon atoms in the aromatic ring, or an aralkenyl radical having 6 to 10 carbon atoms in the aryl portion and 1 to 5 carbon atoms in the alkenyl portion; the substituents of each of said substituted aryl radical being one or more radicals selected from the group consisting of: (1) alkyl or alkoxy containing from 1 to 5 carbon atoms; (2) nitro; (3) aryloxy containing from 6 to 10 carbon atoms; (4) halogen; and (5) a polymer to which the aryl radical is attached as a dependent moiety, the polymer having at least one repeating unit which is a lower alkylene containing from 1 to 5 carbon atoms.

Claim 13

An element as defined in claim 10, and further including, in admixture with said binder, a spectral sensitizing compound having a λ max in methanol which is less than about 450 nm, said compound being one that, when co-dissolved with a sulfonamide polymer and an amount of said cyclopropenone effective to photogenerate an image, forms a composition which can be dried in a layer and which upon imagewise exposure demonstrates a spectral response at a wavelength that is (a) longer than the limit of the spectral sensitivity of the cyclopropenone and (b) still within absorbence region of said compound.

Claim 14

An element as defined in claim 11, wherein said spectral sensitizing compound is 2-benzoyl-methylene-3-methylnaphtho-(2,1-a)thiazoline.

Claim 15

A process for forming a photographic image, comprising the steps of: (a) imagewise-exposing to activating radiation a radiation-sensitive photographic element containing an admixture of a polymeric binder and a decomposable radiation-sensitive cyclopropenone having a λ max in ethanol which is no greater than about 400 nm in the spectral range of about 250 to about 650 nm to form a developable latent image in said element, and (b) developing the resulting image by heating said element to a temperature and for a time sufficient to force CO bubbles formed by the photodecomposition of the agent to expand to form a visible image.

Claim 16

A process for forming a photographic image, comprising the steps of: (a) imagewise-exposing to activating radiation a radiation-sensitive photographic element containing an admixture of a polymeric binder and a decomposable radiation-sensitive cyclopropenone having a λ max in ethanol which is no greater than about 400 nm in the spectral range of about 250 to about 650 nm to form a developable latent image in said element, and (b) developing the resulting image by heating said element to a temperature and for a time sufficient to force CO bubbles formed by the photodecomposition of the agent to expand to form a visible image.

Claim 17

The process as defined in claim 13 wherein the cyclopropenone has the formula: ##STR9## wherein: R 1 and R 2 are the same or different, and are each a substituted or unsubstituted aryl radical containing from 6 to 10 carbon atoms in the aromatic ring, or an aralkenyl radical having 6 to 10 carbon atoms in the aryl portion and 1 to 5 carbon atoms in the alkenyl portion; the substituents of said substituted aryl radical being selected from the group consisting of: (1) alkyl or alkoxy containing from 1 to 5 carbon atoms; (2) nitro; (3) aryloxy containing from 6 to 10 carbon atoms; (4) halogen; and (5) a polymer to which the aryl radical is attached as a dependent moiety, the polymer having at least one repeating unit which is a lower alkylene containing from 1 to 5 carbon atoms.

Claim 18

A process as defined in claim 13 wherein said heating is carried out at a temperature within the range of 100° C. to 150° C.