CA2197469A1

CA2197469A1 - Laser addressable thermographic elements

Info

Publication number: CA2197469A1
Application number: CA002197469A
Authority: CA
Inventors: Richard E. Bills; David C. Weigel
Original assignee: Individual
Current assignee: GlassBridge Enterprises Inc
Priority date: 1994-09-27
Filing date: 1995-08-01
Publication date: 1996-04-04
Also published as: IL115056A0; KR970706523A; DE69515496T2; WO1996010213A1; MX9702044A; CN1158660A; EP0783726B1; BR9509042A; DE69515496D1; EP0783726A1; JPH10506339A

Abstract

A thermographic imaging element containing a substrate which is coated on at least one surface thereof with a thermographic imaging system having at least one layer containing light-insensitive organic silver salt; reducing agent for silver ion; a binder; toner; and a dye which absorbs radiation in the wavelength range of about 750-1100 nm. Preferably, there is a layer adjacent to the one containing the light-insensitive organic silver salt, etc., which contains binder and additional dye which absorbs radiation in the range of about 750-1100 nm. When the thermographic imaging element is exposed to radiation of 750-1100 nm of 0.10-2.0 joules/cm2 for 0.20-200 microseconds, an image density of about 1.0 or greater is formed. When imaging a thermographic imaging element with radiation-absorbing dye in both adjacent layers or only the layer containing binder and dye, the radiation is directed through the layer containing the light-insensitive organic silver salt, etc., before striking the adjacent layer containing radiation-absorbing dye and binder.

Description

~ WO96110213 2 1 9 7 ~ 6 q A ~ 1~

LASER ~nn~T~ RTP~ ~P~IC ELEMENT8 ~ Field of the Invention The present invention relates to novel lO th~L - ~hic imaging elements and more particularly, it relates to th~L JL~hic imaging elements that can be directly imaged using an infrared laser diode. The present invention further relates to processes for imaging the inventive thermographic imaging elements 15 using an infrared laser diode.

Back~rouna of the Invention In the imaging arts, imaging elements that can be imagewise exposed by means of light or heat are well 20 known. Silver halide conventional photographic and photothermographic elements are the most representative elements of the class of light-sensitive materials. In both conventional photographic ("wet silver") and photothermographic ("dry silver") elements, exposure of 25 the silver halide in the photosensitive emulsion to light ~Lvduces small clusters of silver atoms tAg~).
The imagewise distribution of these clusters is known in the art as a latent image. Generally, the latent image formed is not visible by ordinary means and the 30 photosensitive emulsion must be further processed in order to produce a visible image. In both dry and wet silver systems the visible image is produced by the reduction of silver ions, which are in catalytic proximity to silver halide grains bearing the clusters 35 of silver atoms, i.e. the latent image. This produces a blacX-and-white image.

~: .

- 21 9746q WO96110~13 l~1~ S .

Conventional photographic silver halide elements require a wet devel-~ L process to render the latent image visible. The wet chemistry used in this process requires special hAn~l ing and disposal of the spent 5 chemistry. The process equipment is large and requires special plumbing.
In photothermographic elements the photographic silver halide is in catalytic proximity to a non-photosensitive, reducible silver source (e.g., silver lO behenate) so that when silver nuclei are generated by light exyo-ure of the silver halide, those nuclei are able to catalyze the reduction of the reducible silver source. The latent image is rendered visible by application of uniform heat across the element.
15 Thermal devices used for developing photothermographic elements address the problems in conventional photographic elements by using a dry process. However, photothermographic elements developed using these devices may have uneven or non-uniform image density, 20 image distortions, and/or surface abrasion defects.
Non-uniform image density defects may occur during the development process due to, for instance, surface variations on the heated member, the presence of foreign matter on the photothermographic element or the 25 heated member, and insufficient allowance for outgassing of volatile materials generated during development. Image distortions can occur due to uncontrolled dimensional changes in the base of the phototh~ hic element during heating and/or 30 cooling of the photothermographic element. Surface abrasions or marring may occur by dragging the photothermographic element across a stationary component in the heating devlce. In many applications, such as text and line drawings, these defects may be 35 acceptable. However, users of medical diagnostic, industrial, graphic arts, printed circuit boards, and ~ WO961~0213 2 ~ 9 7 4 6 9 other imaging applications desire uniform and high quality images.
U.S. Patent No. 5,041,369 describes a process which capitalizes on the advantages of a dry processed 5 photo~he~ -phic element without the need for surface contact with a heating device. The photothermographic element is imagewise exposed with a laser which splits the beam using a second harmonic generation device. In this process, the element is simultaneously exposed lO with one wavelength of light and thermally activated by the absorption of a light-to-heat near-infrared (NIR) dye at the second wavelength of light. Even though this process has the advantage of simultaneous ~X~Oau~ e and heat development of the image, the equipment 15 required is complex and limited by laser outputs capable of generating two useful separate wavelengths.
In addition, the photosensitive emulsion still requires both light and heat activation to generate an image.
Photosensitive emulsions which contain silver 20 halide are well known in the art to be capable of causing high minimum density (Dmin)~ both in the visible and ultraviolet (W) portions of the spectrum.
The high W Dmin is due to the inherent absorption in the near W of silver halides, particularly silver 25 bromide and silver iodide, and to high haze when silver halide and organic silver salts are present together.
High W Dmin is undesirable for graphic arts scanner and imagesetting films since it increases the exposure time required during contact exposure with other media 30 such as W sensitive printing plates, proofing films, and papers. High haze can also lead to loss of image resolution when imaged photothermographic elements are used as contact films. It is also well known that silver halides in photothermographic elements can lead 35 to poor light stability of the background image density leading to fogging.

2~ 97469 WO96110tl3 I~ .c A class of imaging elements that do not rely on silver halide-based chemistry is theL - aphic elements. These materials are widely used in facsimile r-rh;nPC, labels, tickets, charts for recording the 5 output of medical or scientific monitoring apparatus, and the like. In the most common form, the thP -,L~phic element comprises a support carrying a coating of a thermally-sensitive composition comprising a color former, usually a substantially colorless lO electron-donating dye precursor, and a color developer, usually an electron-accepting compound. Heat is imagewise applied to the element by means of a thermal head, a thermal pen or a laser beam, and upon imagewise applied heating, the color former instantaneously 15 reacts with the color developer to form an image. U.S.
Patent No. 4,904,572 describes a thermographic element which uses leuco dyes to enhance the developed image.
A leuco dye is the reduced form of a color-bearing dye.
It is generally colorless or very lightly colored. In 20 this application, silver behenate acts as a Lewis acid which reacts with the leuco dye upon imagewise application of heat to form a colored image. A black image is achieved by the combination of subtractive colors (cyan, yellow, and magenta~. It is well known 25 in the art that it is very difficult to achieve a high density neutral tone black using subtractive colors.
Since the image is generated by colored dye formation, the absorption of the image in the ultraviolet is weak and therefore, provides little utility as a W masking 30 film.
Conventional thermographic films typically require imaging dwell times of from l to 5 seconds . Processing times of this extent are not practical in a laser imaging application. In order to provide an 35 appropriate imaging dwell time for a laser addressable system, there is a need for a thermographic film ~ WO96110213 2 1 9 7 4 6 9 r~ r7 UUna~L ~u~ion which is capable of forming an in-situ image in micros~con~c.
Each of the abu~ ioned classes of imaging elements has some disadvantage. For example, ~ 5 conventional silver halide photographic materials have a high environmental impact due to the wet procpccing ~ chemistry; photothermographic materials have lower image fastness, limited optical density, and poor dimensional stability; silver halide-based emulsions lO typically use visible sensitizers which need to be bleached or removed and need to be handled in the dark or subdued light; both conventional photographic and phototh~L ,L aphic elements require a two-step process ('_X~Oa~L~ and dev~1 ~ t); and conventional 15 thermographic elements require high imaging energy, relatively long thermal imaging dwell times, and have lower image fastness and limited W optical density.
What is needed in the industry are imaging elements and processes which help to overcome the 20 above-disclosed problems. It was against this background that the present inventions were developed.

BummarY of the Invention In one ~ho~i r -nt, the present invention provides 25 a thermographic imaging element comprising a substrate having coated on at least one surface thereof a th~L ~phic imaging system comprising at least one layer comprising light-insensitive organic silver salt;
reducing agent for silver ion; a binder; toner; and a 30 dye which absorbs radiation in the wavelength range of about 750-llO0 nm, wherein the at least one layer comprising the light-insensitive organic silver salt forms an image density of greater than about l.0 when exposed to 0.10-2.0 joules/cm2 of radiation (having a 35 wavelength in the range of about 750-llO0 nm)in 0.2-200 microseconds.

2 1 9 7 4 6 ~

In another Pmho~ir--t~ the present invention provides a th~ , _phiC imaging element comprising a substrate coated with a thermographic imaging system, the th, ~ aphic imaging system comprising at least 5 two adjacent layers, one of the adjacent layers comprising light-insensitive organic silver salt;
reducing agent for silver ion; a binder; toner; and optionally, a dye which absorbs radiation having a wavelength in the range of about 750-llO0 nm and the lO other adjacent layer consisting essentially of dye which absorbs radiation in the wavelength in the range of about 750-llO0 nm and binder such that the layer comprising the light-insensitive organic silver salt forms an image density of greater than about l.0 when lS exposed to O.lO -2.0 joules/cm2 of radiation (having a wavelength in the range of about 750-llO0 nm)in 0.2 -200 microseconds.
In a further Pmho~ L, the present invention provides a prccess for forming an image comprising the 20 step of exposing a thermographic imaging element comprising a substrate coated ~ith a thermographic imaging system, comprising at least one layer comprising light-insensitive organic silver salt;
reducing agent for silver ion; a binder; a dye which 25 absorbs radiation in the wavelength range of about 750-llO0 nm; and toner, to radiation in the range of about 750-llO0 nm such that the at least one layer comprising the light-insensitive organic silver salt forms an image density of greater than about l.0 when exposed to 30 O.lO - 2.0 joules/cm2 of radiation in (having a wavelength in the range of about 750-llO0 nm) in 0.2 -200 microsecon~q.
In still another embodiment, the present invention provides a process for forming an image comprising the 35 step of exposing a thermographic imaginq element comprising a substrate coated with a thermographic ~ WO96110213 2 1 974 69 J~

imaging system, the ~h~ ,L~phic imaging system comprising at least two~adjacent layers, one of the adjacent layers comprising light-insensitive organic silver salt; reducing agent for silver ioni a binder;
5 toner; and optionally, a dye which absorbs radiation having a wavelength in the range of about 750-1100 nm and the other adjacent layer consisting essentially of binder and dye which absorbs radiation having a wavelength in the range of about 750-1100 nm, to 10 radiation having a wavelength range of about 750-1100 nm which is directed to the thermographic imaging element through the layer comprising the light-insensitive organic silver salt before striking the adjacent layer consisting essentially of binder and dye 15 such that the layer comprising the light-insensitive organic silver salt forms an image density of greater than about 1.0 when exposed to 0.10 - 2.0 joules/cm2 of radiation ~having a wavelength in the range of about 750-1100 nm) in 0.2 - 200 microseconds.
In a preferred Dmho~; - ~ nt to the above inventions, an image density of greater than about 2.00 and, more preferably, greater than about 2.50, and most preferably, greater than about 2.75 comprising metallic silver is formed in the layer comprising light-25 insensitive organic silver salt, reducing agent, etc., upon exposure to 0.10 - 2.0 joules/cm2 of radiation (having a wavelength in the range of about 750-1100 nm)in 0.2 - 200 microsecon~c.
The layers ("theL ,L~phic silver emulsion 30 layers") comprising light-insensitive organic silver salt, reducing agent for silver ion, etc., in all of the above-disclosed Pmho~ir~nts of the present invention can incorporate up to about 1.0 wt% silver halide, based upon the total weight of the layer.
The silver-based thermographic imaging elements and methods for using the thermographic imaging 3 21 9746q l~lIL~__.'O~

elements as laser addressable direct-write fllm provided by the present invention ~v~ many of the problems seen in current systems. Since the thl , a~hic imaging element is thorr~lly-sensitive~
5 rather than photosensitive, it is white light-handleable and does not require removal of a visible sensitizer. Unlike wet silver and photothermographic elements, no post-processing steps are required for development of the image. When a high power laser lO diode is scanned across the thermographic imaging element, an in-situ black image is printed out in the th -_ ~phic silver emulsion, thus enabling many useful applications such as an on-line inspection system for printed circuit board phototool mask 15 production. In addition, heat shrinkage of the film is minimized since only the imaged portion of the emulsion is heated and the temperature of the substrate is relatively unchanged. This is ocperi~lly important for applications where registration is critical, such as 20 image-setting films for color reproduction and printed circuit board phototools. In addition, the ~h~ ~ ~phic imaging element is capable of producing high resolution halftone images which are useful in color reproduction processes.
Other aspects, advantages, and benefits of the present invention are apparent from the detailed description, the examples, the drawings, and the claims.

Brief DescriDtion of the D~awin~s FIG. l shows a schematic representation of a laser sensitometer.
FIG. 2 shows a graph of distance versus the relative intensity of a laser diode comparing the plots 35 for theoretical versus actual profile data for a flat-topped cone shaped laser spot on the film plane.

~ WO 96110~13 2 1 9 7 4 6 q FIG. 3a shows a graph of the total incident e~o-uLe energy plotted against the distance across the laser beam in the cross/scan direction.
FIG. 3b shows a microdensitometer profile of a S line imaged with the energy profile depicted in FIG.
3a onto a thermographic element. (Example 16, Sample N
not shown.) FIG. 4 shows a graph of density versus the log of the e~o~uLe using the data shown in FIG. 3a.
FIG. 5 shows a graph of absorption versus wavelength comparing the imaged and non-imaged areas of a fh~ ~,LaphiC imaging element. (Example 16, Sample N
not shown.) Det~iled DescriPtion of the Invention As used herein, "thermographic imaging element"
refers to a substrate coated on at least one surface thereof with a ~l~hP r,Laphic imaging system". The thermographic imaging system comprises at least one theL-~,Laphic silver emulsion layer containing light-20 insensitive organic silver salt; reducing agent for silver ion; binder; toner; and a dye which absorbs radiation having a wavelength in the range of about 750 - 1100 nm. Additionally, the thermographic imaging system may comprise a layer adjacent to the 25 thermographic silver emulsion layer which contains further radiation-absorbing dye and binder.
In the present invention, the thermographic silver emulsions which are utilized comprise a light-insensitive silver salt; a reducing agent for silver 30 ion; a dye which absorbs radiation having a wavelength in the range of about 750-1100 nm; a toner, binder; and an optional development accelerator.
The light-insensitive silver salts are materials, which in the presence of a reducing agent, undergo 35 reduction at elevated temperatures, e.g., 60~-225~C, to form silver metal. Preferably, these materials are _g_ wo g6~l0~l3 2 ~1 9 7 4 6 9 ~ 5 ~

silver salts of long chain alkanoic acids (also knoun as long chain aliphatic carboxylic acids or fatty acids) containing 4 to 30 carbon atoms; more preferably, 8 to 28 carbon atoms; and most preferably, 5 10 to 22 carbon atoms. The latter are also known in the art as "silver soaps".
Non-limiting examples of silver salts of aliphatic carboxylic acids include silver behenate, silver stearate, silver oleate, silver erucate, silver lO laurate, silver caproate, silver myristate, silver pa~mitate, silver maleate, silver ~umarate, silver tartarate, silver linoleate, silver camphorate, and mixtures thereof. Complexes of organic or inorganic sllver salts wherein the ligand has a gross stability 15 constant between 4.0 to 10.0 can also be used. Silver salts of aromatic carboxylic acids and other carboxyl L~LUU~ ~OIlLailling ~ C include silver benzoate, a substituted silver benzoate such as silver 3,5-dihydroxybenzoate, silver o-methylbenzoate, silver 20 m-methylbenzoate, sllver p-methylbenzoate, silver 2,4-dichlorobenzoate, silver acetamidobenzoate, silver p-phenyl benzoate, etc., silver gallate, silver tannate, silver phthalate, silver terephthalate, silver salicylate, silver phenylacetate, silver pyromellitate, - 25 silver salts of 3-carboxymethyl-4-methyl-4-thiazoline-2-thiones or the like as described in U.S.
Pat. No. 3,785,830; and silver salts of aliphatic carboxylic acids containing a thioether qroup as disclosed in U.S. Pat. No. 3,330,663. Silver salts of 30 _ olln~ containing mercapto or thione groups and derivatives thereof can also be used. Preferred examples of these compounds include silver 3-mercapto-4-phenyl-1,2,4-triazolate, silver 2-mercaptobenzimidazolate, silver 2-mercapto-5-35 amino~h~ olate, silver 2-(S-ethylglycolamido)benzothiazolate; silver salts of ~ Wos6/10213 2~ 97469 r~.,. ~ . .

t_ioglycolic acids such as silver salts of S-alkyl thioglycolic acids (wherein the alkyl group has from 12 to 22 carbon atoms~; silver salts of dithiocarboxylic acids such as silver dithioacetate, silver 5 thio~mi~ate, silver 1-methyl-2-phenyl-4-thiopyridine-5-carboxylate, silver triazinethiolate, silver 2-sulfidoh~n7~Yazole; and silver salts as disclosed in U.S. Pat. No. 4,123,274. Furthermore, silver salts of a compound containing an amino group can be used.
10 Preferred examples of these compounds include silver salts of benzotriazoles, such as silver benzotriazolate; silver salts of alkyl-substituted benzotriazoles such as silver methylbenzotriazolate, etc.; silver salts of halogen-substituted 15 benzotriazoles such as silver 5-chlorobenzotriazolate, etc.; silver salts of carboimi~h~n7Otriazoles, etc.;
silver salts of 1,2,4-triazoles and l-H-tetrazoles as described in U.S. Pat. No. 4,220,709; silver salts of imidazoles; and the like. Preferably, the light-20 insensitive silver salt material should constitute from about 5 to 60% by weight and more preferably, from about 30 to 50% by weight, based upon the total weight of the thermographic silver emulsion layer.
Any reducing agent for silver ion can be used in 25 the present invention. Such reducing agents are well-known to those skilled in the art. Examples of such reducing agents include, but are not limited to, methyl gallate; hindered phenols; catechol; pyrogallol;
hydroquinones; substituted-hydroquinones; ascorbic 30 acid; ascorbic acid derivatives; leuco dyes; and the like. The most preferred reducing agents are methyl gallate, butyl gallate, and propyl gallate. Whatever reducing agent is employed in the present invention is preferably used in an amount of about 5.0 to 25.0% by r 35 weight and more preferably, from about 10.0 to 20.0% by WO96/10213 2 1 9 7 4 6 9 r ~ 5 ~

weight, based upon the total weight of the th~ phic silver emulsion layer.
Toners are also used in the thermographic silver ~ lcion layer(s~. Examples of toners include 5 phthalazinone, phthalazine, barbituric acid, sllccin;m;~e~ and phth~lim;de. Combination of toners have been found to be especially useful, the preferred combinations being phthalazinone with barbituric acid and phthalimide with barbituric acid and most preferred 10 being succinimide with barbituric acid. The toner(s) should preferably be present in an amount in the range of about 0.2 to 10.0~ by weight; more preferably, about 1.0 to 8.0% by weight; and most preferably, about 2.0 to 6.0% by weight, based upon the total weight of the 15 thermographic silver emulsion layer.
AnY11 i ~ry reducing agents or development accelerators may be optionally included in the thermographic silver emulsion layer ~p~n~ing upon the silver source used. Preferably, the auxiliary reducing 20 agent comprises a 3-indazolinone or urea compound as a development accelerator.
3-indazolinone - ~n~c used in the present invention preferably have the following structure:

~""

wherein R is selected from the group consisting of:
hydrogen; an alkyl group of 1 to 4 carbon atoms;
halogen; -COOH and -RlCOOH wherein Rl is an alkyl group having from 1 to 4 carbon atoms. Preferably, R is 35 hydrogen or an alkyl group having from 1 to 4 carbon atoms and most preferably, R is hydrogen.

~ WO9~10213 2 1 9 7 4 69 ~I/L~

Such 3-indazolinone _ '- can be synthP~; 70~
according to procedures well known to those skilled in the art of synthetic organic chemistry. Alternatively, such materials are cially available, such as from 5 Aldrich Chemical Company of Milwaukee, Wisconsin;
Lancaster ~hP~irAl Company of Windham, New ~ -~ire;
~ and K&K Laboratories of Cleveland, Ohio.
As is well understood in this area, a large degree of substitution is not only tolerated, but is often 10 advLsable. Thus, as used herein the phrase "group" is intended to include not only pure hydrocarbon substituents such as methyl, ethyl, and the like, but also such hydrocarbon subctituents bearing conventional substituents in the art such as hydroxy, alkoxy, 15 phenyl, halo (F, Cl, Br, I), cyano, nitro, amino, etc.
Urea compounds used in the present invention preferably have the following formula:
o wherein R2 and R3 each independently represent hydrogen; a Cl-Cl0 alkyl or cycloalkyl group; or phenyl; or R2 and R3 together form a heterocyclic group 25 containing up to 6 ring atoms. Preferably, R2 and R3 represent ll~dLUY~I; a C1 to C~ alkyl or cycloalkyl group; or phenyl; or R2 and R3 together form a heterocyclic group containing up to 5 ring atoms. Such urea _ -ullds can be readily synthesized and are 30 commercially available. Non-limiting examples of such urea compounds include urea; 1,3-diphenyl urea; 1,3-diethyl urea; butyl urea; and 2-imidazolidone. The most preferred development accelerator is 2-imidazolidone.
The thermographic imaging elements of the present invention are not light-sensitive in the traditional sense and therefore, do not need to contain photosensitive agents such as silver halides;

W096tlO213 2 1 9 7 4 6 9 1~I/L~

photoinitiator; or photogenerated bleaching agents.
The ~h- -, ~phic silver emulsion layers can have less than 1%, less than 0.75%, less than 0.5%, or 0% by weight, based upon the total weight of the 5 thermographic silver emulsion, and perform well. The silver halide is deemed to be ineffective if it does not catalyze formation of a latent image.
Light stabilizers such as benzotriazole, phenylmercaptotetrazole, and other light stabilizers 10 known in the art may be added to the thermographic silver emulsion. The preferred light stabilizer is benzotriazole. The light stabilizer should preferably be present in an amount in the range of about 0.1% to 3.0% by weight of the thermographic silver emulsion 15 layer and more preferably, from 0.3 to 2.0 wt%.
The thermographic silver emulsion layer utilized ln the present invention also employs a binder. Any conventional polymeric binder known to those skilled in the art can be utilized. For example, the binder may 20 be selected from any of the well-known natural and synthetic resins such as gelatin, polyvinyl acetals, polyvinyl chloride, cellulose acetate, polyolefins, polyesters, polystyrene, polyacrylonitrile, polycarbonates, and the like. Copolymers and 25 terpolymers are, of course, included in these definitions, examples of which, include, but are not limited to, the polyvinyl aldehydes, such as polyvinyl acetals, polyvinyl butyrals, polyvinyl formals, and vinyl copolymers. Preferably, the binder should be 30 present in an amount in the range of 10 to 50~ by weight and more preferably, 15 to 50% by weight, based upon the total weight of the thermographic silver emulsion layer.
The thermographic element of the present invention 35 employs a dye which absorbs electromagnetic radiation having a wavelength in the range of between about 750-~ WO96~10213 2 1 9 7 4 6 9 , ~

llO0 nm, preferably in the range of about 750-900 nm, and most preferably, in the range of about 750-870 nm.
The dye should be soluble in the coating solvent, preferably ketones or aromatic solvents, such as methyl - 5 ethyl ketone or toluene. The dye should also be miscible with the binder and compatible with the silver salts, activators, and developers used in the emulsion.
For use in W (ultraviolet) contact film or mask applications the optical density of the dye is lO preferably greater than l.0 optical density units with a concomitant weak absorption of less than 0.2 optical density units in the W region corresponding to the wavelength of ~OSUL e devices for which the material will be used as a mask (250-450 nm). The optical 15 density is measured using a ~acBeth Model TDS23 densitometer eguipped with a status 18A filter. It is also desirable, but not necessary, for the dye to have a low visible background absorption.
The radiation-absorbing dye can be employed in the 20 same layer as the light-insensitive organic silver salt; reducing agent for silver ion; toner; and binder.
Alternatively, the dye can be employed in the foregoing layer as well as in an adjacent layer or primarily in the adjacent layer. The radiation-absorbing dye may be 25 added directly to the thermographic silver emulsion layer or indirectly by allowing the dye to migrate from the adjacent layer, containing the dye, into the theL -, ~p1.ic silver emulsion layer during the manufacturing process of the thermographic imaging 30 element.
Suitable dyes include, but are not limited to, oxonol, squarylium, chalcogenopyrylarylidene, bis(chalcogenopyrylo)polymethine, bis(aminoaryl)polymethine, merocyanine, trinuclear 35 cyanine, indene-bridged polymethine, oxyindolizine, ferrous complex, quinoid, nickel dithiolene complex, .

and cyanine dyes such as carbocyanine, aza~a~bo~anine, hemicyanine, styryl, diazacarbocyanine, triazacarbocyanine, diazahemicyanine, polymethinecyanine, azapolymethinecyanine, holopolar, 5 indocyanine, and ~i~ 7 ~ h Pm i cyanine dyes.
The amount of dye present in the th~L ,L aphic imaging element will be ~PpP~dP~t upon whether the dye is incuL~o,ated solely into the thermographic silver emulsion layer or in an adjacent layer as well. When lO the dye is present solely in the thermographic silver emulsion layer, the dye will be present in an amount of from 0.10-5.0 wt~ and preferably from 0.2 - 3.0 wt%, based upon the total weight of the thermographic silver emulsion layer.
When present in an adjacent layer, the dye will be present in the thermographic silver emulsion layer in an amount of from 0 - 5.0 wt% and preferably, from about 0 - l.0 wt~, based on the total weight of the thermographic silver emulsion layer. In the adjacent 20 layer containing dye and binder, the dye will be present in an amount of from 1-25 wt~ and preferably, 5 - 20 wt%, based upon the total weight of the adjacent layer.
Any suitable base or substrate material known to 25 those skilled in the art can be used in the present invention. Such materials can be opaque, translucent, or transparent. Commonly employed base or substrate materials utilized in the thermographic arts include, but are not limited to, paper; opaque or transparent 30 polyester and polycarbonate films; and sppc~ rly light reflective metallic substrates such as silver, gold, and aluminum. As used herein, the phrase 'lsppr~llarly light reflecting metallic substrates" refers to metallic substrates, which when struck with light, 35 reflect the light at a particular angle as opposed to reflecting the light across a range of angles.

~ w09~02~3 - 21 9 74 69 r~

Optionally, a protective or anti-stick layer, positioned on top of the theLIr, ~phic imaging element, may be used. Any conventional anti-stick material may be employed in the present invention. Examples of such 5 anti-stick materials, include, but are not limited to waxes, silica particles, styrene-containing elastomeric block copolymers such as styrene-butadiene ~LyLane, styrene-isoprenc ~LyL~ne, and blends thereof with such materials as cellulose acetate, cellulose acetate 10 butyrate, cellulose acetate propionate, and poly(vinyl butyral).
Additional layers may be in~GL~oL~ted into the thermographic elements of the present invention such as a primer layer or anti-static layer. Furthermore, an 15 anti-static or anti-stick layer may optionally be applied to the back of the support. Materials for such purposes are well known to those skilled in the art.
The th~. .,L~phic imaging system, anti-stick, infrared or near-infrared dye absorbing, and anti-20 static layers employed in the present invention can beapplied by any conventional method such as knife coating, roll coating, dip coating, curtain coating, hopper coating, etc. If desired, two or more layers may be coated simultaneously by the procedures 25 described in U.S. Patent No. 2,761,791 and British Patent No. 837,095.
The th~ phic imaging elements of the present invention are imaged by ~o~u~e to infrared or near-infrared laser radiation, typically from a infrared or 30 near-infrared laser diode. As is well known in the thermal imaging arts, infrared or near-infrared laser diodes may be advantageously arranged in an array to increase imaging speed. Lasers that can be used to provide infrared or near-infrared radiation include ~ 35 substantially any laser capable of generating light in the infrared and near-infrared region of the ele~LL~ gnetic ~e~L~- from about 750 to 1100 nm, including dye lasers; solid state diode lasers such as ~ m1mlm gallium arsenide diode lasers that emit in the region of 780 to 870 nm; and diodc p, -~ solid state 5 lasers such as Nd:YAG, Nd:YLF, or Nd:glass.
The following non-limiting examples further illustrate the present invention.

UPr.l:!R
Materials used in the following examples are available from standard commercial sources such as Aldrich Chemical Co. (~ilwaukee, WI) unless otherwise specified.
Silver behenate and silver laurate homogenates 15 may be prepared as ~;CClns~d in U.S. Pat. No. 4,210,717 (column 2, lines 55-57) or U.S. Pat. No. 3,457,075 (column 4, lines 23-45 and column 6, lines 37-44).
The following dyes were used in various examples which follow:

SO~NH2 H2NO2S~< Cl N ~ N
Dyel jO3 ~03 ~

Pr~ration of Dve 1: 5-Sulfamoyl-2,3,3-trimethylindolenine was prepared according to the ~ WO96/102U 2 1 9 7 4 6 9 method described in U.S. Patent No. 4,062,682. A
mixture of 37.0g of 5-sulfamoyl-2,3,3-trimethylindolenine, 16.7mL of 2-chloroeth~n~ fonyl chloride, and 200mL of acetonitrile were refluxed for 6 - 5 hours. After the addition of 18.5mL of water, the mixture was stirred overnight. The separated solid was ~ filtered, washed with acetonitrile, and dried to give ll.Og of a 1-sulfoalkylated quaternary salt int~ te.
A mixture of 6.5g of chlorocyclopentene dialdehyde, 26g of the quaternary salt int~ ~iate prepared above, 108mL of acetic anhydride, and 72mL of acetic acid was stirred for 10 minutes at room temperature. After addition of 12.8mL of 15 diisopropylethylamine, the mixture was stirred overnight. The separated solid was filtered, washed with the solvent mixture, and dried to give 20.0g of dye 1.

H2NO2S~X Cl ~

~ ~ N r nye2 Pre~aration of Dve 2: In a 3L flask, 385g of trimethyl sulphonamido indolenine was added with 250mL of butyronitrile. To this mixture was added, with no 25 exotherm, 225mL (364g~ of butyliodide followed ~y 750mL
of additional butyronitrile. The mixture was heated to reflux with efficient overhead stirring for 22.5 hours.
The heat was removed and the mixture allowed to cool to 2 1 974 6~
WO96/10213 r~". ~o about 40~C. Stirring was continued for 1 hour, after the addition of lL of ethylacetate. The solid was filtered, washed with ethylacetate, and dried to give 595.6g of N-butyl-2,3,3-trimethyl-5-sulphonamido 5 indoleninium iodide.
To a solution of 370mL of methylene chloride and 558mL of dimethylformamide, cooled to below 5~C, was added dropwise over 1 hour 277mL of rhncrhnrus oxychloride at a rate such that the temperature did not 10 exceed 5~C. After the completion of the addition, the external cooling was removed and the mixture was stirred for 1 hour. Over a 30 minute period, 75mL of cyclopentanone was added in two portions. After the first addition, a slow increase in temperature and 15 color was observed to about 35~C, at which time the second portion was added resulting in a large exotherm.
After the exotherm subsided, the mixture was heated to reflux for 4 hours. The mixture was distilled under a slight vacuum after the addition of lL of ethylacetate.
20 Approximately 250mL of liquid was collected to which 700mL of ethylacetate was added when a precipitate started to form. The mixture was stirred overnight. The solid was filtered, washed with lL of ethylacetate, followed by heptane, and dried under vacuum at 35~C for 25 4 hours giving rise to 115.8g of crude chlorocyclopentene dialdehyde.
The crude chlorocyclopentene dialdehyde was dissolved in 1250 mL of water. crystals started to appear after about 1 hour. The mixture was allowed to 30 stand over the weekend. The brownish solid was filtered, washed with water, and dried under vacuum at 35~C for 7 hours giving rise to 61.0g of chlorocyclopentene dialdehyde.
To a solution of 450mL of acetic acid and 450mL of 35 acetic anhydride was added 278.7g of N-butyl-2,3,3-trimethyl-5-slllrhon~mi~ indoleninium iodide and 47.6g ~ WO96~10213 2197469 r .,. . ~

of cyclopentene dialdehyde. To the stirred mixture was added dropwise 90mL of triethylamine over 5 minutes at 60-65~C. No large exotherm was observed. The mixture was heated for an additional 30 minutes, after which - 5 the heat was removed and the reaction mixture cooled to 15~C. The resultant golden-brown solid was filtered and washed with a 1:1 mixture of acetic acid:acetic ~nhydride until the washings were greenish rather than purple. Residual acetic acid and acetic anhydride were 10 removed by suspending the solid in lL of ethyl acetate, followed by stirring for so minutes. The solid was filtered and washed with ethyl acetate. The filtrate had a pink hue. The solid was dried at 45~C under vacuum overnight giving rise to 250.0g of Dye 2.

SO~
~o2S ~ a ~
~N/~N ~ Dye 3 Pre~aration of Dve 3: A mixture of 0.1 moles of Dye 2 20 prepared above, 0.1 moles of sodium tetraphenylborate, and 500mL of methanol was refluxed with stirring for 10 minutes. The solid was filtered, washed with methanol, followed by water, and then dried to give 0.97 moles of Dye 3.

WO96/10213 . ?l9 74 69 rcl,u~c~

o- Dye 4 H ~ ~ " H

Hgc>(~ ><CHg Pr~n~ration of Dve 4: A stirred mixture of 26.05g of 1,8-di~min~n~rhthalene, 32.66g of 2-tride~nnn~, 55mg of p-toluenesulfonic acid monohydrate, and 250mL of toluene was heated to reflux under a nitrogen 15 at~ ph~re using a Dean-Stark trap to remove the water evolved from the reaction for 5 hours. The mixture was then washed with saturated sodium bicarbonate solution, dried over anhydrous potassium carbonate, filtered, and the solvent removed under reduced pressure. The 20 product was distilled to yield 48.86g of dihydroperimidine intermediate; b.p. 192-213~C at 0.3 to 0.4 torr.
A stirred mixture of 8.0g of the dihydroperimidine intermediate prepared above, 1.48g of squaric acid, 25 64mL of n-butanol, and 64mL of toluene was heated to reflux under a nitrogen atmosphere using a Dean-Stark trap to remove the water evolved from the reaction for 3 hours. The mixture was filtered, poured into 600mL
of petroleum ether (b.p. 35-60~C), and kept at 5~C for 30 18 hours. The product was f iltered of f, washed with petroleum ether, and air dried to give 6.45g of Dye 4.

' 2 1 97469 ~ 5~-~

OCH~
CHJo~mX a ~o; Nl~
- 5 ~ ~ ~ ~ ~ 9~N ~
N~O9S '~' ~ ~ ~ SO;N~ Dye 5 SOJ

15 PreParation of DYe 5: With stirring, 28g of 2,3,3-trimethyl-5-methoxyindolenine was added to 80mL of fuming sulfuric acid ~10% of 5O3). The mixture was stirred overnight at room temperature and then poured onto 500g of crushed ice. The aqueous solution was 20 neutralized with a 30% sodium hydroxide solution and evaporated to dryness under vacuum. The residue was extracted with methanol and the solution evaporated.
The solid was picked up in ethanol, filtered, washed with ethanol and dried under vacuum to give 20g of an 25 indolenine sulfate salt intermediate as yellowish prisms.
A mixture of 20g of the indolenine sulfate salt int~ te prepared above, 20g of 2,4-butanesulfone, and 80mL of benzonitrile was refluxed with stirring for 30 5 hours. The solid formed was filtered, washed with ethylacetate, and dried under vacuum to give 25g of a sulfonalkylated quaternary salt intermediate as light-brown prisms.
A mixture of 14.2g of the sulfonalkylated 35 quaternary salt intermediate prepared above, 7.5g of N-(2-chloro-3-(dimethylamino)methylene)-1-cyclohexen-1-~096110213 2 ~ 9 7 4 6 9 ~ 7 ~

yl~_ethylene)-N-methylme~h~n~min1um chloride (prepared as described in EPO Application No. 0288261~, 5.4mL of dicyclohexylethylamine, and 75mL of benzonitrile was stirred at room temperature overnight. The mixture was 5 filtered and the ~iltrate added to ethylacetate. The solid was filtered and dried. The solid was dissolved in 50mL of ethanol and 3g of sodium iodide added. The precipitate was filtered, washed with acetonitrile, and dried to give 3g of Dye 5 as green prisms.

~ ~3 ~3 ~ 3 H3C ~
-CH ~ I ~ Dye 6 ( ~ 4so3Na ( ~ ~SO3 Dve 6 is commercially available from Eastman Kodak Co., Rochester, NY.

r les 1-3 The following coating solutions were used in the preparation of Examples 1-3:

Silver E~llcion:
Silver behenate homogenate 160g (10% by weight in methyl ethyl ketone) Butvar B76 poly(vinyl butyral~, available from 20g ~onsanto Co.

~hermogramhic Coatin~ Solutions:

~ WO96110213 2 1 9 74 69 .~-I/U~ 5,~

The ~he , GphiC coating solutions for Examples 1-3 were y~.pa~ed by mixing the following ingredients with 20g of the silver emulsion described above:

5 ~aterial Example 1 Ex~mple 2 Example 3 Methyl Gallate 0.6g 0.6g 0.6g Pyrogallol 0.2g 0.2g 0.2g Phthalazinone 0.2g 0.2g 0.2g Succinimide O.lg O.lg O.lg 10 2-imidazolidone O.lg O.lg O.lg Barbituric acid 0.05g 0.05g Benzotriazole 0.02g Each of the solutions were coated onto a 0.08mm t3 15 mils) polyester substrate at a O.lmm (4 mils) wet thickness and air dried at 60~C for 3 minutes.
An infrared-absorbing topcoat solution was prepared by mixing 0.08g of Dye 1, l.Og of CA 398-6 cellulose acetate resin, and 20.0g MEK. The topcoat 20 solution was coated onto the thermographic layer at a 0.05mm (2 mils) wet thi~kn~c and air dried for 3 minutes at 60~C.

E~ples 4-6 The following coating solutions were used in the preparation of Example~ 4-6:

Silver E~yl~iQn:
Silver laurate full soap hr , n~te 160g (10% by weight in methyl ethyl ketone) BX-l poly~vinyl butyral), available from lOg Sekisui ~h~m; r~ 1 CO.

35 Thermo~ra~hic Coating Solutions:

2 1 9 7 4 6 q The th~L _ ~phic coating solutions for r l~c 4-6 were prepared by mixing the following ingredients with 20g of the silver emulsion described above:

N~terial Ex~mplo ~ Examplo 5 Example 6 Methyl Gallate 0.6g 0.6g 0.6g Pyrogallol 0.2g 0.2g 0.2g Phthalazinone 0.2g 0.2g 0.2g 10 Succinimide O.lg O.lg O.lg 2-imidazolidone O.lg O.lg O.lg Barbituric acid 0.05g 0.05g Benzotriazole 0.02g Each of the solutions were coated onto a 0.08 D (3 mils) polyester substrate at a O.lmm (4 mils~ wet thickness and air dried at 60~C for 3 minutes.
An infrared-absorbing topcoat solution was prepared by mixing 0.08g of Dye 1, l.Og of CA 398-6 20 cellulose acetate resin, and 20.0g MEK. The topcoat solution was coated onto the thermographic layer at a 0.05mm (2 mils) wet thickness and air dried for 3 minutes at 60~C.
Table 1 summarizes the results of exposing the 25 materials of Examples 1-6 with a 810 nanometer laser diode (available from Spectra Diode Labs of San Jose, CA) at 1.75 J/cm2 focused on the film plane at (a 7 micron spot size). The visible optical densities were measured using a Perkin Elmer microdensitometer PDS
30 lOlOM and the W optical densities were measured using a MacBeth TD523 densitometer equipped with a status 18A
filter. The W light stability was de~ermined by ~ WO961~0~13 2 i 9 7469 .~ s~i- .

allowing the sample to stand in a fluu~3cent (1,000 foot candles, so~Fj light box for 24 hours.

~able 1 Example l 2 3 ~ 5 6 Visible Dmax3.06 3.23 3.25 3.87 3.84 3.83 Visible Dmin0.05 0.05 0.05 0.07 0.07 0.07 UV Dmin 0.15 0.14 0.13 0.19 0.15 0.16 ~V Dmin 0.55 0.61 0.23 0.53 0.59 0.25 24hr stability Examples 3 and 6 clearly show a significant ~ uv~ -~t in UV Dmin light stability when benzotriazole is added to the thermographic silver emulsion.

Exam~le 7 The f ollowing coating solutions were used in the preparation of Example 7:

Silver r lsion:
Silver behenate homogenate (10~ by weight in methyl ethyl ketone) 160g BX-1 poly(vinyl butyral), available from Sekisui Chemical Co. lOg Thermoqra~hic Coatinq Solution.
The th~ , aphic coating solution was prepared by adding 20g of the silver emulsion to 0.6g of methyl gallate, O.lg of succinimid~ O.lg phth~limide~ O.lg 35 tetrachlorophthalic anhydride, 0.02g of benzotriazole, 0.05g of barbituric acid with 4mL of methanol, and lmL

WO96/10213 2~97469 .~ J~-S ~

of MEK. The solution was coated onto a 0.08mm (3 mils) polyester substrate at a 0.08mm (3 mils) wet thickness and air dried at 60~C for 3 minutes.
An infrared-absorbing topcoat solution was 5 prepared by mixing 0.08g of Dye 1, 0.5g of Sekisui BX-l poly(vinyl butyral), and 20.0g MEK. The topcoat solution was coated onto the thermographic layer at a 0.05mm (2 mils) wet thickness and air dried for 3 minutes at 60~C.
Example 7 was exposed with a 810 nanometer laser diode (available from Spectra Diode Labs of San Jose, CA) at 1.75 J/cm2 focused on the film plane at (a 7 micron spot size). The imaged film gave rise to a visible Dmax of 3.4, visible Dmin of 0.08, W Dmax of 15 3.6 and W Dmin of 0.17. The visible optical densities were measured using a Perkin Elmer microdensitometer PDS lOlOM. The W optical densities were measured using a MacBeth Model TD523 densitometer equipped with a status 18A filter.
~x~mPle 8 The following coating solutions were used in the preparation of Example 8:

25 Silver Emulsion:
Silver behenate homogenate 160g (10% by weight in methyl ethyl ketone) BX-l poly(vinyl butyral), available from 15g Sekisui Chemical Co.
30 Acryloid A-21 acrylic resin, available from 6g Rohm and Haas Methyl ethyl ketone (MEK) 50g 35 Th~LI..4~rauhic Coatin~ Solution:
The thp ,LaphiC coating solution was prepared by adding 15g of the silver emulsion to 0.6g of methyl ~ W096/10213 21 9 74 69 r ., gallate, O.lg phth~lA7inon~ O.lg 2-imidazolidone, O.lg tetrachlorgFh~h~l i r anhydride, 0.05g of barbituric acid with 4mL of methanol, lmL of MEK, and lmL of tetralLydLuruL~n. Before coating, 0.13g of Dye 1 was ~ 5 added to the solution. The solution was coated onto a 0.08mm (3 mils) polyester substrate at a 0.08mm t3 - mils) wet thir~nPcc and air dried at 50~C for 3 minutes.
A topcoat solution containing a 2.4~ by weight 10 solution of BX-l poly(vinyl butyral) was overcoated onto the thermographic layer at a 0.05mm (2 mil) wet thic~n~cc and air dried at 50~C for 3 minutes.

Examples 9-10 The following coating solutions were used in the preparation of Examples 9-10:

Silver Em~lcion:
Silver behenate homogenate 160g (10% by weight in methyl ethyl ketone) BX-1 Poly~vinyl butyral), available from 5g Sekisui ~h~mic~l Co.

25 Thermoqra~hic Coat~inq Solution:
The thermographic coating solutions were prepared by adding 15g of the silver emulsion to 0.6g of methyl gallate, O.lg of succinimide, O.lg of 2-imidazolidone, O.lg of tetrachlorophthalic anhydride, 0.05g of 30 barbituric acid with 4mL of methanol, and lmL of MEK.
Before coating, 0.08g of Dye 2 was added to the solution in Example 2 and 0.08g of Dye 3 was added to the solution in Example 3. The solution was coated onto a 0.08mm (3 mils) polyester substrate at a 0.08mm (3 mils) wet thickness and air dried at 50~C for 3 minutes.
A topcoat solution containing a 2.4% by weight solution of BX-1 poly(vinyl butyral) was overcoated 2 1 9 7 4 6 9 ~.,~

onto the th~L - ~phic layer at a 0.05mm (2 mils) wet thickness and air dried at 50OC for 3 minutes.

r les 11-12 5 The following coating solutions were used in preparation of Examples 11-12:

silver Emulsion:
Silver behenate homogenate 160g (10% by weight in methyl ethyl ketone) Butvar B-76 poly(vinyl butyral) 20g TheL ._La~hic Coatina Solution:
The thermographic coating solution was yL~a~ed by adding 15g of the silver emulsion to 0.8g of methyl gallate, 0.2g of succinimide, O.lg of phthalaz,inone, O.lg of 2-imidazolidone in 4mL of methanol, and lmL of methyl ethyl ketone. Before coating, 0.05g of Dye 4 20 was added to the solution in Example 11 and 0.08g of Dye 5 was added to the solution in Example 12. The solutions were coated onto a .08mm (3 mils) polyester substrate at a O.lmm (4 mils) wet thickness and air dried at 21~C for 10 minutes.
A topcoat solution containing a 2.4~ by weight solution of CA398-6 cellulose acetate, available from Eastman Kodak Co., was overcoated onto the thermographic layer at a O.O5mm (2 mils~ wet thickness and air dried at 21~C for 20 minutes.
Table 2 summarizes the results of exposing the materials of Examples 8-12 with a 810 nanometer laser diode (available from Spectra Diode Labs of San Jose, CA) at 1.75 J/cm2 focused on the film plane at (a 7 micron spot size). Maximum (DmaX) and minimum (Dm~n) 35 optical densities were measured using a MacBeth Model TD523 densitometer equipped with a status 18A filter.

WO96110213 I~
~ 2~9746~
T~ble 2 Example # 8 9 10 11 12 EX~U~ULe time 72 45 45 45 72 (microseron~c) D~.y 3.2 3.01.55 2.5 3.1 W Dmjn 0.19 0.160.13 0.180.18 Visible D~ n O . 07 0.070.07 0.070.13 ~Yam~le 13 To show the effect of having halide ion present in the thermographic silver emulsion, 0.2g of calcium bromide was added to the thermographic coating solution of Example 9. The thermographic layer turned totally 15 blacX when air dried at 21~C for 3 minutes.

~Y~mnle 14 The following coating solutions were used in the preparation of Example 14:
20 Silver E~lcion:
Silver behenate homogenate 160g (10~ by weight in methyl ethyl ketone) Butvar B-76 poly(vinyl butyral) 20g Th~L ~ hic Coatinq Solution:
The thermographic coating solution was prepared by adding 0.6g of methyl gallate, 0.2g of phthalazinone, O.lg of succin;mide~ O.lg of 2-imidazolidone, and 0.2g 30 of pyrogallol to 20g of the silver emulsion. The solution was coated onto a .08mm (3 mils) polyester substrate at a O.lmm (4 mils) wet ~hir~nPsc and air dried at 21~C for 10 minutes.
An infrared-absorbing topcoat solution was 35 prepared by mixing 0.03g of Dye 6, l.Og of CA 398-6 cellulose acetate resin, and 20.0g MEK. The topcoat solution was coated onto the th- D r aphic layer at a . .

WO96/10213 2 l 9 7 4 6 ~

O.O5mm (2 mils) wet ~hirkn~cc and air dried for 3 minutes at 60~C.

~y~m~le ~5 The following coating solutions were used in the preparation of Example 15:

Silver F~llcion:
Silver behenate homogenate 160g tlOi by weight in methyl ethyl ketone1 Butvar~ B-76 poly(vinyl butyral) 20g The~ phic Coatinq Solution:
The thermographic coating solution was prepared by adding 0.6g of methyl gallate, O.lg of succinimide, O.lg of 2-imidazolidone and 0.2g of L-ascorbic acid palmitate to 20g of the silver emulsion. The solution was coated onto a .08mm (3 mils) polyester substrate at 20 a O.lmm (4 mils) wet thickness and air dried at 60~C
for 3 minutes.
An infrared-absorbing topcoat solution was prepared by mixing 0.03g of Dye 6, l.Og of CA 398-6 cellulose acetate resin, and 21.0g MEK. The topcoat 25 solution was coated onto the thermographic layer at a 0.05mm (2 mils) wet thickness and air dried for 3 minutes at 60~C.
Table 3 summaries the laser exposure results for each example. Maximum and minimum optical densities 30 were measured using a MacBeth Model TD523 densitometer equipped with a status 18A filter.
Table 3 Example 14 15 Dmax 3.73 2.73 Dmin 0.10 ~ ~os6l~02~3 21 97469 1~., J;-f~

The radiation-absorbing dye may be incorporated primarily into the thermographic silver emulsion layer.
It is believed that the th~ -, aphic silver emulsion layer is heated above its glass transition temperature, -5 thereby allowing the reducing agent for silver ion to migrate to the light-insensitive organic silver salt ~(e.g., silver behenate) within the layer. The silver behenate is reduced by the reducing agent to elemental silver, forming a brown/black image. Toners are 10 incorporated into the formulation to obtain a more neutral black color. The formation of the elemental silver in the imaged area not only provides W opacity of the image in the final element, but also is an infrared-absorber which accelerates the image-forming 15 process. The intensity of the infrared laser beam decreases exponentially as it penetrates into the thermographic silver emulsion layer. The thickness of the thermographic silver emulsion layer and the concentration of infrared dye will effect the sharpness 20 of the image due to the decreasing intensity of the laser beam as a function of distance through the layer.
The thickness of the thermographic silver emulsion layer is preferably between about 1 and 10 microns and more preferably, between about 2 and 6 microns. The 25 concentration of the infrared dye and the thickness of the layer is adjusted such that the IR absorption of the layer is generally between 20% to 99~; preferably, 50 - 90%; and more preferably, 60 - 85%.
In high resolution imaging conditions, where the 30 pixel dwell time is short and the laser peak intensity is high, ablation may occur if the infrared dye is incorporated solely in the thermographic emulsion layer ~of the construction. The heating rate is higher at the surface where the laser beam enters into the 35 thermographic silver emulsion layer. As the elemental silver forms, the absorption of the laser beam WO96110213 .~

lncreases. This can cause the ~hP ~hic silver ~ 1 ~inn layer to overheat, thereby causing smoke, damage, or ablation.
By eliminating or decreasing the concentration of 5 infrared dye in the th- -, ~phic silver emulsion layer and adding infrared dye in a layer adjacent to the ~h- -~aphic silver emulsion layer, the penetration of the laser beam into the fhl aphic silver emulsion layer can be increased. The thermographic imaging 10 element is exposed by directing the laser beam through the thermographic silver emulsion layer before striking the adjacent layer containing infrared dye. The infrared-absorbing layer can be positioned either above or below the thermographic silver emulsion layer 15 relative to the substrate upon which the adjacent layers are deposited. The concentration of infrared dye in the infrared-absorbing layer is chosen such that the highest heating rate occurs at the interface between the infrared-absorbing layer and the 20 th~L -, ~phic silver emulsion layer. The concentration of infrared dye will depend upon the thickness of the thermographic layer and the physical properties of the dye. For example, the concentration of infrared dye in a 1 micron thick th. ,L~phiC layer is adjusted to 25 achieve an absorption of preferably about 90% or more.
During the course of an imaging laser pulse, elemental silver forms at this interface. The elemental silver formed increases the infrared absorption in this region of the thermographic silver 30 emulsion layer and acts as a heat source for the image area within the th~ aphic silver emulsion layer.
As the elemental silver density i5 built up adjacent to the infrared-absorbing layer, the intensity near the opposite surface of the thermographic silver emulsion 15 layer is attenuated, thus reducing overheating in this region. The profile of the pixel image would resemble ~ wog6no~l3 2 1 9 7 4 6 9 r~"~

an hour-glass shape, thus giving rise to a sharper image.
r,~m~le 16 This example demonstrates the effect of the 5 ~hirknPe5 of the th~ , aphic silver emulsion layer, the resin/silver ratio, the concentration of infrared A dye, and the type of topcoat on the imaging characteristics of the inventive thermographic imaging element.
The following coating solutions are used in preparation of Samples A-P. X are variables specified in Table 4.

Silver Emulsion:
15 Silver behenate homogenate 160g tlO% by weight in methyl ethyl ketone) Butvar~ B-76 poly(vinyl butyral) Xg 20 Thermoqra~hic Coatlnq Solution:
The th~ phic coating solution was prepared by adding 15g of the silver emulsion to 0.8g of methyl gallate, 0.2g of sl~rcinimide~ O.lg of phthalazinone, O.lg of 2-imidazolidone in 4mL of methanol and lmL of 25 methyl ethyl ketone. Before coating, Xg of Dye 2 was added to the solution. The solutions were coated onto a .08mm (3 mil) polyester substrate at X wet thirknPc~
and air dried at 70~C for 3 minutes.
A topcoat solution comprising a 2.4% by weight 30 solution of CA398-6 cellulose acetate; Scripset 540 ~yL~ne -~leic anhydride copolymer available from Monsanto Company;, Tyril 880B styrene-acrylonitrile resin available from Dow Chemical Company, or poly(vinyl alcohol) (PVA), Airvol 523 available from 35 Air Products and Chemicals, Inc., Allentown, PA and X%
Dye 2 was overcoated onto the theL -,L~hic layer at X
wet thirknP~s and air dried at 50~C for 3 minutes.

WO 96110213 2 1 q 7 4 6 9 T~

Samples A-P were scanned with a laser sensitometer at several different 6can 5peed6 ranging from 20 to 60 cm/s. Density profiles of these lines at 415 nanometers were measured using a Perkin-Elmer 5 microdensitometer PDS l0l0M. Optical density measurements were taken at 826 nA- ors (laser diode wavelength) and at 415 nanometers for the unimaged Pl~ ~ u8ing a ~:hir~~7u S~e.;~ul,l.otometer MPC-3 l00/W3 l0 lPC .
Tnbl~
Sarnple # A B C D E F G H
" .'' 0.10 0.05 0.10 0.05 0.10 0.05 0.10 0.10 Layer thicicness (wet, rn n) Top Coat Layor 0 0 0 0 0 0 0.05 005 thicicness (wet, mm) Top Coat Resin none none none none none none PVA PVA
Type Butvar content in20g 208 lOg lOg Sg Sg 0 0 Silver L yer infrareci Dye in O.OSg O.OSg O.OSg O.OSg O.OSg O.OSg 0 0.01gTl _ L yer infrre~iDyein 0 0 0 0 0 0 O.lOg O.lSg Top Coat D min (415mn) 0.95 0.14 1.1 0.3 1.24 0.75 0.34 0.53 Opticai Density 0.65 0.34 0.7 0.36 0.79 0.27 1.80 3.20 oD 825 nm S~nnple~Y I J K L M
Tl _ .- l~yer 0.10 0.05 0.10 0.05 010 thicicness (wet, rmn) Top Coat Layer 0.05 005 005 005 o o5 thicicness (wet, r~n) Top Coat Resin Type Celluiose CelluioseCeliuiose Ceiiulose TyriiTU
Acetate Aceb~te Acetate Acetate Butvar content in10g 10g 10g lOg o Silver I~yer SUBSTITUTE SHEET (RULE 26) WO 96110213 2 1 9 7 4 b 9 P~

t Infiur~ Dyo in 0.07g 0.07g O.lOg O.lOg O.OSg Tl _ , ' ' l~yer Inf~ed Dyo in 0 0 0 0 0 Top Co~t Dmin (415tun) 0.23 0.07 0.42 0.12 0.55 Opticd Density e~ 825 nm 0.75 0.30 1.40 0.84 0.76 Sllmple~ N O P
Tl _ ,' Iayer 0.10 0.10 0.10 tbic~noss (wet, mm) Top Co~lt L~yer 0,05 0.05 0.05 thiclolocs (vvet, rmn) Top Collt ResinTypoScripset~MScripset~ Scnpset~U
Butv~r conterlt in 0 0 0 Silver IJyer Infr~red Dye in O.Olg O.Olg 0 Tl " ,-' I~yer ~nf~red Dyo m 0. IOg 0 158 O.lOg 2 0 Top Coct Dm~ (415~) 0.35 0.29 0.42 Opticd Density all 825 nm 0.84 1.45 1.11 A laser sen6itometer (l), shown in FIG. 1, was 25 used to evaluate the t h~ phic imaging elements in Example 16. A 700 milliwatt beam (2) emitted from a 2361-P2 fiber coupled laser diode (3) (available from Spectra Diode ~abs) was focused onto a rotating drum (4). The core diameter of the fiber (5) was 100 30 micrometers and the wavelength of the laser diode (3) was 826 nanometers. The power on the rotating drum (4) was 210 milliwatts and the spot shape was a flat-topped cone with a spot size of 45 microns at full width half maximum (FWHH). The flat-topped cone profile is 35 characterized by rO, the radius of the peak intensity of the cone, and rl, the outer radius of the cone where the intensity is nearly zero. A sc~nning slit beam SUSSTITUTE SHEET (RULE 26) profiler was used to measure the intensity profile of the laser spot. Since the profiler integrates the intensity in the direction perpendicular to the slit - ~ ~, the actual spot profile was inferred from the 5 profiler data. FIG. 2 shows a comparison of the profiler data (6) and the calculated profile data t7) expected for a flat-topped cone intensity profile with rO equal to 10 micrometers and rl equal to 36 micrometer6. The curve was computed by integrating the 10 model flat-topped cone intensity profile in one direction and rpcral; nq.
As the intensity profile is scanned across the film, points lying under the spot profile will receive a finite exposure energy. This exposure energy is 15 ~f~pan~Pnt upon the location of the point with respect to the scanned spot as well as the spot scan speed.
FIG. 3a shows the total incident exposure energy plotted versus the distance across the beam in the cross/scan direction. The curve was calculated for the 20 fiber-coupled sensitometer model beam shape, aR-nm;nq a scan speed of 40 centimeters/seconds. In FIG. 3b, a microdensitometer profile of a line imaged with the energy profile shown in FIG. 3a, onto the thermographic element is shown. (Example 16, Sample N not shown.) 25 The density data was collected using a narrowband filter at 415 nanometers. The density edges in FIG. 3b exhibit gradients that are larger than that of the incident exposure profile shown in FIG. 3a, indicating that the thf ~l~phic element (Example 16, Sample N
30 not shown) has a high contrast.
The contrast of the fhr~ phic element can be PY~minPd more quantitatively using a D-logE curve. A
D-logE curve is a plot of the imaged film density versus the logarithm of the incident ~X~U~UL a energy.
35 The theoretical form for this curve is given by D =
ylog (EEF/Eo); where y is equal to the slope of the D-~ ~096110213 2 1 9 7 4 6 9 F~./ ~ : .

logE curve, E is equal to the incident exposure energy, EF i8 equal to the fog or backyr~.,d level effective energy, Eo is equal to the minimum energy required to begin development of the image, and D is equal to the 5 optical density of the element when exposed to ex~o energy E. The backyround density i5 equal to ~log EF
Using the data shown in FIG. 3, a D-logE curve was computed and plotted in FIG. 4. From the model curve described by the optical density equation, the gamma or lO contrast of the element corresponds to the slope of the D-logE curve. The gamma value for the D-logE curve in FIG. 4 is 34. For a relative comparison, a typical rapid access wet-processed silver halide film has a gamma of approximately lO. The higher contrast is an 15 advantage for graphic arts applications since high contrast hal~tone dots are desired for consistent tone curve control and also for new stochastic screening processes. Similar advantages apply to printed circuit board phototool applications.
The D-logE curve in FIG. 4 shows that the density development begins at approximately 0.9 J/cm2 and that density saturation at maximum density (DmaX) occurs at l.2 J/cm2. It is to be understood that the optimum imaging speed and scanner exposure conditions will be 25 unique for the particular scanner used to image the thermographic element.
Each of the samples described in Table 4 were scanned with the laser sensitometer (l) of FIG. l at Qeveral different scan speeds ranging from 20 to 60 30 centimeters/second. D-logE curves were calculated with a Perkin-Elmer microdensitometer using the data from the density profiles of these lines at 415 nanometers, The model parameters in the optical density equation described above were determined from the D-logE curves 35 and are summarized below in Table 5.

WO 96/10213 ~ 2 1 9 7 4 6 ~

Tztbl~ i S mpledl A B C D E
Dma ~ 4 5 (415 ~m) mD Eo, 50 0.77 0.85 0.74 0.93 0.60 mD Esat, 501.30 1.40 1.40 1.80 1.23 mD Dma~, 503.50 3.50 3.65 3.50 3.60 mD Dmin, 500.85 0.40 0.55 0.65 0.80 gamma, 50 11.65 14.30 11.19 9-93 8.98 mD Eo, 100 0.966 0.94 0.96 1.00 1.03 mD Dsat, 1001.27 1.30 1.26 10.00 1.32 mD Dmal~, 100 3.5 3.0 3.4 0.0 3.6 mD Dmin, 1000.80 0.35 0.80 0.00 0.80 gamn~a, 10022.7~ 18.82 22.02 0.00 25.99 Gamma 100 1.95 1.32 1.97 0.00 2.89 /Gamlna 50 Sample~ E 1 ~ K L
Dma~ (415 nm) mD Eo, 50 0.65 0.80 1.13 0.56 0.35 mD Esat, 501.60 1.26 2.00 1.30 1.00 mD Dnw, 50 3.70 3.60 3.50 3.70 3.60 mD Dmin, 500.70 0.40 0.30 0.60 0.35 gamma, 50 7.80 16.22 12.90 8.47 7.12 mD Eo, 100 1.00 0.90 1.00 0.66 0.661 mD Dsat, 10010.001.16 10.00 1.00 1.042 mD Dma~, 1000.0 3.5 0.0 3.6 3.5 mD Dmin, 1000.00 0.30 0.00 0.70 0.40 gamma, 100 0.00 29.03 0.00 16.07 15.88 Gamma 100 0.00 1.79 0.00 1.90 2.20 IGamma 50 WO 96/10213 2 1 9 7 4 6 9 ~ c S~lmplelt N O
DrGa~ (415 nm) 5.00 4.4 mD Eo, 50 0.95 0.88 mD Es t, 50 1.65 1.26 mD Dmax, 50 3.70 3.80 mD Dmin, 50 0.70 0.50 gamma, 50 12.51 21.16 mD Eo, 100 0.96 0.97 mD Dsat, 1001.20 i.76 mD Dmax, 100 3.7 3.8 mD Dmin, 1000.40 0.50 ganuna, 100 34.05 29.05 Gamma 100 2.72 1.37 /Gamma 50 mD Eo,S0 = Eo value from D-lo~E curve, scan spoed at 20 . '. ' (cmts) mD Esat,S0 e Esst valuc from D-logE curve, scam speed ~t 20 cmts mD Dmax,50 = Maximum Density at 20 cmts mD Dmmn,50 = Minimum Density at 20 cmts 20 gamm~,S0 = ~mma value when scanning at 20 cmts mD Eo,100 = Eo value from D-loxE curvo, scan speed at 40 cmts mD Esat,100--Esat value from D-lo~E curve, sc n speed at 40 cmls mD Dmax,100 = Maximum Density at 40 cmts mD Dmin,100 = Minimum Density at 40 cmls 25 ~amma,100 ~ gamma value when scannin~ 40 cmts gnmma 100/gamma 50 = (gamma st 40 cmls) divi~le~l by (~amma at 20 cmts) The average value Eo for samples A through L is 0. 8 + 0 . 2 Joules/cm2 at a scan speed of 20 cm/s and 0.9 30 + 0.2 Joules/cm2 at a scan speed of 40 cm/s. The minimuD e~o~uLe energy re~uired to begin density development is relatively independent of the scan speed. The Esat values are ;n~r~pPn~Pnt of speed as well. The average value for Esat is 1.3 + 0.2 35 Joules/cm2 at a scan speed of 20 cm/s and 1.2 + 0.1 Joules/cm2 at a scan speed of 40 cm/s. The gamma values show evidence of imaging performance differences at the two speeds. The average gamma value for Samples A through ~ at a scan speed of 20 cm/s is 12 + 4 while 21 ~746q WO96110213 I~

the average gamma value at 40 cm/s is 24 i 6. Thus.
the gamma values appear to increase significantly as the scan speed is increased. It is possible that at the lower scan speeds the heat diffusion i5 more 5 significant giving rise to loss of sharpness of the edges and thus, reducing the gamma of the image.
Unlike photothermographic silver media, thermographic silver elements show a more pronounced effect of ~O~UL e conditions.
Samples C, I, and K were coated with different infrared dye concentrations. Samples C and I have an 80% absorption at the laser diode wavelength of 826 nanometers. Sample K was coated to the same thickness, but was loaded with more infrared dye so that it 15 absorbs 96% at 826 nanometers. The average Eo and Esat values for C and I are 0.93 Joules1cm2 and l.21 Joules/cm2, respectively, at a scan rate of 40 cm/s.
The Eo and Esat values for Sample K are 0.66 Joules/cm2 and l.0 Joules/cm2, respectively. The sensitivity of 20 the film appears to be slightly improved by the 16%
increase in the layer absorption.
The effect is more pronounced for thinner coatings. Samples D, J, and L were coated at half the thi~kn~ss of C, I, and K. Samples D and J absorb only 25 about 50% of the incident laser radiation, and do not image at the 40 cm/s scan rate. Sample L absorbed 85%
of the incident laser radiation. The average Eo and Esat values for D and J are l.0 Joules/cm2 and l.9 Joules/cm2, respectively at 20 cm/s, whereas the Eo and 30 Esat values for Sample L are 0.35 Joules/cm2 and l.0 Joules/cm2, respectively. The ~O~ULe energy values ~or L are lower than that of D and J. Sensitivity is ~nh In~d with increasing laser absorption in the thermographic silver emulsion layer, or with increasing 35 infrared dye conc~ L~tion. The edges of the imaged lines scanned at 40 cm/s in Samples K and L were 21 ~7469 ~096~02~3 smoother than the other single infrared layer samples.
The line edge sharpness can be improved by increasing the infrared dye concentration in the layer.
A comparison of samples with different ~ 5 thi~nP~epe~ but similar absorption percentages, indicates that a thinner coating with a higher infrared dye ~oncell~Lation is more sensitive than one with a thicker coating. The Eo and Esat values for R are 0.56 and 1.3 Joules/cm2, respectively, at 20 cm/s, whereas 10 the Eo and Esat values for L are 0.35 and 1.0 Joules/cm2, respectively. The thickness of Sample L is half that of K, but it absorbs 85~ of the laser radiation, which is roughly comparable to that of K.
Increasing the infrared dye concentration may cause 15 ablation due to increased peak temperatures in the th~. ~ aphic layer. The sensitivity of a single thermographic silver emulsion layer containing infrared dye can be r-Yimi7ed by coating the thermographic silver emulsion layer as thin as possible with the 20 highest achievable infrared dye concentration, while maintaining the desired maximum density.
The quality of the imaged line is affected by the resin to silver ratio. The exposure energy values and the gamma values are not significantly affected by Z5 changes in the resin to silver ratio, as shown in Table 5 for Samples A, C, and E. However, the micrographs of these samples indicate that the resin to silver ratio does affect the image quality of thc lines. As the resin to silver ratio is decreased, the edges of the 30 lines become rough and jagged, and the density uniformity across and along the imaged line decreases.
Decreasing the resin concentration should enhance the sensitivity of the material due to less bulk material to heat. However, the jagged edges appear to have 35 offset this advantage. The resin to silver ratio is preferably between about 25 - 50 wt~.

Wo96/10213 2 1 9 7 4 6 9 r~l,. 5 96~1 Another ~mhoA i r ~ t of the present invention comprises the addition of infrared dye in a layer adjacent to the ~h~ ,LGphiC silver emulsion layer.
Samples N, 0, G, H, and P in Example 16 evaluate the 5 addition of an infrared dye in the topcoat of a thermographic element. For some unknown reason, Samples M, G, and H imaged poorly and therefore, are not included in Table 4. Samples N, 0, and P exhibited improved line quality compared to the samples lO containing infrared dye in the th~ ,LGphic layer only. The thermographic silver layers in Samples N, 0, and P were overcoated with a .05 millimeter coating of Scripset resin that contains a high concentration of infrared dye. A piece of pressure-sensitive adhesive 15 tape was used to separate the topcoat from the thermographic silver emulsion layer to verify that the two layers had not intermixed. Samples N and 0 have gamma values greater than 34 and 30, respectively, at a scan speed of 40 cm/s. These gamma values are 20 comparable to a conventional silver halide duplication film. For comparison, a typical rapid access silver halide film has a gamma of approximately lO. The quality of Sample P is similar to N and 0, although a D-log E curve was not computed for this sample. Both N
25 and 0 exhibit sharp smooth line edges with an approximate l micron edge roughn~CC. The samples containing infrared dye in the thermographic silver layer only had rougher edges than Samples N and 0. The density uniformity of Samples N, 0, and P were within 30 +5%. The sensitivity of Samples N and 0 are comparable to the samples having no topcoat containing infrared dye. No ablation was observed in Samples N, 0 and P.
Improved edge contrast, edge sharpness, and density uniformity can be achieved by the addition of infrared 35 dye in a layer adjacent to the thermographic silver layer. In addition, the susceptibility to ablation is - 21 974 69 r~ J -also reduced in this cvn~LLu~Lion. The concer.LL~tion of the infrared dye in the th~ -,L~pllic silver layer i5 in an amount such that the absorption Or the laser radiation in the th. , ~phiC layer is preferably less ~ 5 than or equal to 40~ and more preferably, less than or equal to 35%.
FIG. 5 shows the imaged t8) and non-imaged (background) (9) transmission spectra for Example 16, Sample N. The ~nhAncPd infrared dye absorption peak at 10 820 nanometers is clearly evident. The density at the laser diode wavelength of 826 nanometers increases from 0.84 (14.5~ transmission) to 1.26 (5.5% transmission), while the density at 415 nanometers increases from 0.355 t44.2~ transmission) to 5.0 (nearly 0%
15 trAn~ sion). The elemental silver formed in the thermographic layer during ~O~UL a provides an ~nhAnre~ absorption difference in the ultraviolet (W), which is an advantage in UV mask applications. In Table 5, the D~aX measured by the microdensitometer was 20 3.7 which is lower than the value obtained from the spectrophotometer. Apparently, the maximum optical density that can be measured by the microdensitometer is limited to about 3.7. This implies that many of the gamma values computed in Table 5 are lower than the 25 true values and therefore, should be treated as ~rv~tive estimates.
In order to compare the imaging characteristics of the thermographic elements with little or no effects due to heat dissipation, Examples 1, 2, 3, 4, 5, 6 and 30 16 (Sample N) were imaged using a 150 milliWatt (110 milliWatts at the image plane) laser diode (SDL-5422, available from Spectra Diode Labs) emitting at 811 nanometers. The beam was focused to an 8 micrometer spot size (full width at 1/e2 level) and scanned at 213 35 centimeters/second with a 4.5 micrometer cross scan llne spacing. Table 6 summarizes the results from this evaluation.

. Table 6 Exzunpl~ Dmax, Dmin, Dmax- Dmax, Dmin, Dmax-365nm365nmDmin, 415nm 415nmDmin, 365nm 415nm 1 2.170.31 1.85 2.48 0.2s 2.23 2 2.580.39 2.19 2.94 0.29 2.65 3 1.780.39 1.39 1.85 0.29 1.56 4 3.050.63 2.42 3.13 0.57 2.56 10 S 4.500.57 3.93 S.00 0.42 4.58 6 4.04o.90 3.14 S.00 O.S9 4.01 16, 4.400.47 3.92 S.00 0.53 4.46 8ampln U

The data shows that the higher contrast(Dmax-Dmin) films are achieved when silver laurate is used in combination with barbituric acid in the thermographic ~ silver emulsion layer (Examples 5 and 6) or a higher concentration of methyl gallate is used in the silver 20 behenate formulation (Example 16, Sample N~. In order to provide workable W contract applications, the contrast is preferably greater than about 2.50. The data also shows that the addition of benzotriazole inhibits the speed Or the film; however, the decrease 25 in speed is minimized when silver laurate is used for the silver soap. Even though a slight decrease in speed may be observed, the improved light stability, as shown in Table l, provides an advantage for jnm~ ng benzotriazole in the th~ ~~ mphic silver emulsion.
pP~c~n~hle variations and modifications are possible from the foregoing disclosure without departing from either the spirit or scope of the present invention as defined in the claims.

Claims

What is Claimed is:

1. A thermographic imaging element comprising a substrate having coated on at least one surface thereof a thermographic imaging system comprising at least one layer comprising light-insensitive organic silver salt;
reducing agent for silver ion; binder; light stabilizer; toner; and a dye which absorbs radiation in the wavelength range of 750-1100 nm, wherein said at least one layer comprising said light-insensitive organic silver salt forms an image density greater than about 1.0 when exposed to 0.10 - 2.0 joules/cm2 of said radiation in 0.20 to 200 microseconds.

2. The element of Claim 1 wherein said image density is greater than about 2.00 and comprises metallic silver.

3. The element of Claim 1 when said image density is greater than about 2.50 and comprises metallic silver.

4. The element of Claim 1 wherein said image density is greaater than about 2.75 and comprises metallic silver.

5. The element of Claim 1 wherein said dye absorbs radiation in the wavelength range of about 750 to 900 nm.

6. The element of Claim 1 wherein said thermographic imaging system further comprises a development accelerator.

7. The element of Claim 1 where said light-insensitive organic silver salt is a silver salt of a carboxylic acid containing 10-30 carbon atoms.

8. The element of Claim 7 where said silver salt is silver behenate or silver laurate.

9. The element of Claim 6 wherein said development accelerator is one selected from the group consisting of:
(i) a 3-indazolinone compound of the formula:

wherein: R is selected from the group consisting: of hydrogen; an alkyl group of 1 to 4 carbon atoms; halogen; -COOH; and R1COOH
wherein R1 is an alkyl group of 1 to 4 carbon atoms; and (ii) a urea compound of the formula:

wherein: R2 and R3 each independently represent hydrogen; a C1 to C10 alkyl or cycloalkyl group; or phenyl; or R2 and R3 together form a heterocyclic group containing up to 6 ring atoms.

10. The element of Claim 9 wherein R represents hydrogen ; R2 and R3 each independently represent a C1 to C5 alkyl or cycloalkyl group; or phenyl; or R2 and R3 together form a heterocyclic group containing up to 5 ring atoms.

11. The element of Claim 1 wherein said toner is at least one selected from the group consisting of phthalazinone, phthalazine, barbituric acid, succinimide, and pthalimide.

12. A thermographic imaging element comprising a substrate coated with a thermographic imaging system, said thermographic imaging system comprising at least two adjacent layers, one of said adjacent layers comprising light-insensitive organic silver salt;
reducing agent for silver ion; toner; binder; light stabilizer;
and optionally, a dye which absorbs radiation having a wavelength in the range of about 750-1100 nm; and said other adjacent layer consisting essentially of binder and said dye which absorbs radiation in the wavelength range of about 750-1100 nm, wherein said layer comprising said light-insensitive organic silver salt forms an image density or greater than about 1.0 when exposed to 0.10 - 2.0 joules/cm2 of said radiation in 0.20 to 200 microseconds.

13. The element according to Claim 12 wherein said light-insensitive organic silver salt is a silver salt of a carboxylic acid containing 10-30 carbon atoms.

14. The element according to Claim 12 wherein said silver salt of a carboxylic acid is silver behenate or silver laurate.

15. The element according to Claim 12 wherein said thermographic imaging system further comprises a development accelerator.

16. The element according to Claim 15 wherein said development accelerator is selected from the group consisting of:

(i) a 3-indazolinone compounds of the formula:
wherein: R is selected from the group consisting of hydrogen; an alkyl group of 1 to 4 carbon atoms; halogen; -COOH; and R1COOH wherein R1 is an alkyl group of 1 to 4 carbon atoms; and (ii) a urea compound of the formula:

wherein: R2 and R3 each independently represent hydrogen; a C1 to C10 alkyl or cycloalkyl group; or phenyl; or R2 and R3 together form a heterocyclic group containing up to 6 ring atoms.

17. The element according to Claim 16 wherein R
represents hydrogen; R2 and R3 each independently represent a C1 to C5 alkyl or cycloalkyl group; or phenyl; or R2 and R3 together form a heterocyclic group containing up to 5 ring atoms.

18. The element according to Claim 12 wherein said dye absorbs radiation having a wavelength in the range of from about 750 to 900 nm.

19. The element according to Claim 12 wherein said image density is greater than about 2.00 and comprises metallic silver.

20. The element according to Claim 12 wherein said image density is greater than about 2.50 and comprises metallic silver.

21. The element according to Claim 12 wherein said image density is greater than about 2.75 and comprises metallic silver.

22. The element according to Claim 12 wherein said toner is at least one selected from the group consisting of phthalazinone, phthalazine, barbituric acid, succinimide, and pthalimide.

23. A process for forming an image comprising the step of exposing a thermographic imaging element comprising a substrate coated with a thermographic imaging system, said thermographic imaging system comprising at least one layer comprising light-insensitive organic silver salt; reducing agent for silver ion; a dye which absorbs radiation in the wavelength range of about 750-1100 nm; toner; light stabilizer; and binder, to radiation having a wavelength in the range of about 750-1100 nm wherein said at least one layer comprising said light-insensitive organic silver salt forms an image density of greater than about 1.0 when exposed to 0.10 - 2.0 joules/cm2 of said radiation in 0.20 - 200 microseconds.

24. The process according to Claim 23 wherein said light-insensitive organic silver salt is a silver salt of a carboxylic acid containing 10-30 carbon atoms.

25. The process according to Claim 24 wherein said silver salt of a carboxylic acid is silver behenate or silver laurate.

26. The process according to Claim 23 wherein said thermographic imaging system further comprises a development accelerator.

27. The process according to Claim 26 wherein said development accelerator is selected from the group consisting of:
(I) a 3-indazolinone compound of the formula:

wherein: R is selected from the group consisting of hydrogen; an alkyl group of 1 to 4 carbon atoms; halogen; -COOH; and R1COOH wherein R1 is an alkyl group of 1 to 4 carbon atoms; and (ii) a urea compound of the formula:

wherein: R2 and R3 each independently represent hydrogen; a C1 to C10 alkyl or cycloalkyl group; or phenyl; or R2 and R3 together form a heterocyclic group containing up to 6 ring atoms.

28. The process according to Claim 27 wherein R
represents hydrogen; R2 And R3 each independently represent a C1 to C5 alkyl or cycloalkyl group; or phenyl; or R2 and R3 together form a heterocyclic group containing up to 5 ring atoms.

29. The process according to Claim 23 wherein said dye absorbs radiation having a wavelength in the range of from about 750 to 900 nm.

30. The process according to Claim 23 wherein said image density is greater than about 2.0 and comprises metallic silver.

31. The process according to Claim 23 wherein said image density is greater than about 2.50 and comprises metallic silver.

32. The process according to Claim 23 wherein said image density is greater than about 2.75 and comprises metallic silver.

33. The process according to Claim 23 wherein said toner is at least one selected from the group consisting of phthalazinone, phthalazine, barbituric acid, succinimide, and pthalimide.

34. A process for forming an image comprising the step of exposing a thermographic imaging element comprising a substrate coated with a thermographic imaging system, said thermographic imaging system comprising at least two adjacent layers, one of said adjacent layers comprising light-insensitive organic silver salt;
reducing agent for silver ion; toner; binder; light stabilizer;
and optionally, a dye which absorbs radiation having a wavelength in the range of about 750-1100 nm and said other adjacent layer consisting essentially of binder and said dye which absorbs radiation in the wavelength range of about 750-1100 nm, to radiation having a wavelength range of about 750-1100 nm which is directed to said thermographic imaging element through said layer comprising said light-insensitive organic silver salt before striking said adjacent layer consisting essentially of binder and said dye which absorbs radiation such that said layer comprising said light-insensitive organic silver salt forms an image density of greater than about 1.0 when exposed to 0.10 - 2.0 joules/cm2 or said radiation in 0.20 to 200 microseconds.

35. The process according to Claim 34 wherein said light-insensitive organic silver salt is a silver salt of a carboxylic acid containing 10-30 carbon atoms.

36. The process according to Claim 34 wherein said silver salt of a carboxylic acid is silver behenate or silver laurate.

37. The process according to Claim 34 wherein said thermographic imaging system further comprises a development accelerator.

38. The process according to Claim 37 wherein said development accelerator is selected from the group consisting of:
(i) a 3-indazolinone compound of the formula:

wherein: R is selected from the group consisting of hydrogen; an alkyl group of 1 to 4 carbon atoms; halogen; -COOH; and R1COOH
wherein R1 is an alkyl group of 1 to 4 carbon atoms; and (ii) a urea compound of the formula:

wherein: R2 and R3 each independently represent hydrogen; a C1 to C10 alkyl or cycloalkyl group; or phenyl; or R2 and R3 together form a heterocyclic group containing up to 6 ring atoms.

39. The process according to Claim 38 wherein R
represents hydrogen; R2 and R3 each independently represent a C1 to C5 alkyl or cycloalkyl group; or phenyl; or R2 and R3 together form a heterocyclic group containing up to 5 ring atoms.

40. The process according to Claim 34 wherein said dye absorbs radiation having a wavelength in the range of from about 750 to 900 nm.

41. The process according to Claim 34 wherein said image density is greater than about 2.00 and comprises metallic silver.

42. The process according to Claim 34 wherein said image density is greater than about 2.50 and comprises metallic silver.

43. The process according to Claim 34 wherein said image density is greater than about 2.75.

44. The process according to Claim 34 wherein said toner is at least one selected from the group consisting of phthalazinone, phthalazine, barbituric acid, succinimide and pthalimide.

45. The process according to Claim 34 wherein said dye which absorbs radiation having a wavelength of from about 750-1100 nm is present in both adjacent layers.