US3716366A

US3716366A - Bis-pyridinium salt and a phenyl boranate as photosensitive combination

Info

Publication number: US3716366A
Application number: US00111764A
Authority: US
Inventors: O Riester
Original assignee: Agfa Gevaert AG
Current assignee: Agfa Gevaert AG
Priority date: 1970-02-19
Filing date: 1971-02-01
Publication date: 1973-02-13
Anticipated expiration: 1990-02-13
Also published as: FR2078870A5; CH553425A; DE2007524A1; GB1293111A; CA973418A; BE762918A

Abstract

Dark colored images are obtained by imagewise exposure of lightsensitive layers containing bis-pyridinium compounds and organic boran compounds as explained below.

Description

United States Patent 1191 I Riester 111 3,716,366 1451 Feb. 13,1973

BIS-PYRIDINIUM SALT AND A PHENYL BORANATE AS h PHOTOSENSITIVE COMBINATION Inventor: Oskar Riester, Leverkusen, Germany Assignee: Ag'f a-Gevaert Aktiengesells chaft,

LeverkusemGermany Filed: Feb. 1', 1971 v Foreign Application Priority Data Feb. 19, 1970 Germany ..P 20 07 524.5

us. c1 .,96/ss, 96/90 PC 7 Int, Cl ..'......G03c 1/00, G036 1/52 Field 61 seal- 11 "96/88, 90 PC Dark colored images are obtained by imagewise expo- 8/1971 Webster 61 a1. ..96/90 Primary ExaminerJ. Travis Brown 7 Assistant Examine rWon H. Louie, Jr. Attorney-Connolly and H'utz ABSTRACT sure of light-sensitive layers containing bis-pyridinium compounds and organic boran compounds as explained below.

4 Claims, No Draivings low.

. 1 BlS-PYRIDINIUM SALT AND A PHENYL BORANATE AS PHOTOSENSITIVE COMBINATION The invention relates to light-sensitive materials which contain, as light-sensitive substances, bispyridiniumcompounds which are converted into dark colored substances by the action of light.

"Numerous processes in which light-sensitive organic substances are used '-for recording images are known.

Some of these processes are based on' photochemical. rearrangements or on reactions of organic compounds which result in a color change. Such photochemical reactions of organic compounds have been comprehensively described e.g. in Praparative organisch'e Photochemie" (A; Schonberg, Springer-Verlag 1958) and in -Light-Sensitive Systems (J. Kosar, John Wiley and Sons, New York, 1965).

These reactions include. e.g. the formation of monomethine dyes by the photolysis of trihaiome'thyl compounds in UV light in the presence of aromatic or heterocyclic, compounds which by virtue .of their constitution haveCH ring-members which are highly reactive in condensation or diazo coupling reactions.

In these processes, these layers are either initially light-sensitive or the reactive components for the photochemical reactionmust be added'before exposure. The systems previously known are only of limited utility because their sensitivityto light is generally too A certain improvement has beenprovided by the .light-sensitive materials described in 'French Pat.

specification No. 1,526,496. These materials contain cyclic imides of aryl polycarboxylic acids in which the imide nitrogen is substituted with olefinically'unsatu light-sensitive materials which are free from silver ha-,

lides, which materials have sufficient sensitivity to light and yield sufficiently deeply colored reactionproducts.

Another object of the invention lies in the production of photographic recording materials in which the image produced on exposure can be extinguished either spontaneously or by additional measures so that the material can be used again. a

I now have found that photographic materials which contain a V a light-sensitive composition of phenyl boranates and .bis-pyridi nium salts are suitablefor recording images. Suitable compounds maybe represented by the following formulas:

1 orr=c11 .-\N:( R(anion) I R! i i cation 1 ku v h I in which lo R represents (I) an aliphatic group containing up to 18 carbon atoms, preferably up to five carbon atoms, which may be saturated or'unsaturated and may contain further substituents, e.g., phenyl,

- halogen such as fluorine, chlorine or bromine,

hydroxyl which may be esterified, in particular with short chain aliphatic carboxylic acids containing up' to six carbon atoms, carboxyl, esterified carboxyl in which short chain aliphatic alcohols are particularly suitable for the ester component,v 20 acyl, especially acyl radicals derived from short chain aliphatic carboxylic acids, sulfonamide in v which the amide group may be substituted with al- .kyl, aryl, especially phenyl, acyl which is .ad-

vantageously derived from short chain aliphatic carboxylic acids or benzene carboxylic acids, or

another sulfonamide group, (II) a cycloalkyl group, e.g., cyclopentyl or cyclohexyl, or (Ill) an aryl group, in-particular a radical of the phenyl or naphthylseries which may be substituted in the same way as the aliphatic radical mentioned under R' represents fan aryl group such as phenyl or naphthyljini particular aradical of the phenyl series; these rings may also be interconnected and this radical may carry other substituents, e.g.', al-

kyl, preferablycontaining up to five carbon atoms, halogen such as chlorine or bromine, hydroxyl, falkoxy, carboxyl, esterified carboxyl, nitro," riitrile, carbamoyl, sulfonic acid, sulfonaniideor sulfonic 40 I acid ester groups;

R" represents a nitrile or R" groupi The nature of'th'e anion or cation is not critical. It will depend mainly on the method ofpreparation used for the above components. Suitable anions are,'e.g., ha-

lide ions, especiallychloride or bromide, sulfate ions,

sulphonate ions such as toluene sulfonate and methane sulfonate, etc. v I

Suitable cations are protons or-cations of the alkali metals, depending on the-pH of thesolution of the components or the pH of the layer. Cations of the alkaline earth metals or ammonium. ions which may carry organic substituents may, of course, also be .used. The only essential condition for the light sensitivity of the material ac'cordingto the invention is the simultaneous presence of bis-pyridiniurn ions and phenyl boranate ions. I I The followingare examples-of suitable compounds:

Bis-pyridinium cations? v N-CiHs 2 i-toluene sulfonate) Phenyl boranates The above compounds are prepared by known methods. For the bis-pyridinium compounds, reference may be made, for example, to the publication by E. Weitz, Zeitschrift fur Ang. Chemie, 1954, page 657 et seq and for the phenyl boranates to the publication by G. Wittig, Ann. 563 (1949) page 114.

The bis-pyridinium compounds and phenyl boranates need not be present in stoichiometric quantities in the light-sensitive material. It is sufficient if one of the components is present in an amount of about to 90 percent by weight based on the total weight of the components. The mixture of compounds preferably contains about 40 to 60 percent by weight of one of the compounds.

The photochemical reaction of the above mentioned compounds will take place both in solution and in the solid phase. In practice, these substances are applied to any layer support either singly or mixed or as mixtures of several bis-pyridinium compounds or phenyl boranates, dissolved or finely divided, with or without binder. The substances are applied by known methods consisting of application or spraying of solutions or casting from solutions or suspensions with layer forming natural colloids or synthetic resins. Suitable for this purpose are gelatine, cellulose, cellulose esters, cellulose ethers, polycarbonates, especially those based on bis-phenylol alkanes, polyesters, especially those based on polyethylene terephthalate, polyamides, polyurethanes and various film-forming polymers or copolymers of olefinically unsaturated monomers such as vinyl chloride, vinyl acetate, styrene, olefinically unsaturated carboxylic acids, their esters or other derivatives such as maleic acid anhydride, acrylic acid or methacrylic acid and their derivatives, as well as polyethylene or polyvinylidene chloride, e.g., in the form of their aqueous dispersions.

The bispyridinium compounds may also be contained in a separate layer and the boron compounds may be contained in a second layer which is in contact with the first.

The usual materials are suitable as layer supports, e.g., paper, glass or natural or synthetic materials such as cellulose esters, especially cellulose acetate or cellulose acetobutyrates, polyesters, especially those based on polyethylene terephthalate, polycarbonates, particularly those derived from bis-phenylol alkanes,

polystyrene or the like. The layer supports may be transparent or contain pigments such as titanium dioxide, barium sulphate, etc. The'surface'of the layer support may be smooth or profiled.

The substances for use according to the invention may, of course, be added directly to the layer support. In the case of a layer support of paper, it is sufficient, e.g., to simply to bathe the support material in a solution of the components.

The light-sensitive compound for use according to the invention may also be applied in self-supporting layers. Layer binders of the type mentioned above are also suitable for this purpose. in principle, it is immaterial which layer binder is used and a suitable layer binder can easily be chosen by simple tests from the wide variety of known natural or synthetic hydrophilic or hydrophobic layer forming substances.

Suitable solvents for the compounds for use according to the invention are, e.g., water, short chain aliphatic alcohols such as methanol or ethanol, acetone, dimethyl formamide or the like.

The concentration of the light-sensitive substances in the binder may be varied within any limits. The gradation or maximum density can be influenced by'varying the concentration as well as the application. When using binders which swell in water, e.g., gelatine, the pH may be varied within the limits at which no significant change takes place in the binder, such as degradation in the case of gelatine. The substances are advantageously used in quantities of l to percent, based on the dry layer. I

Casting additives, e.g., wetting agents or compounds which improve the mechanical properties (e.g., hardness) may be added to the layers.

On exposure to light, the light-sensitive compounds used in the materials according to the invention yield colored products which are stable for several hours to several days, depending on the nature of the reactants and the structure of the light-sensitive layer.

they remain visible for some time. Hydroxyl-substituted V aromatic compounds, particularly those of the phenyl or naphthyl series, e.g., hydroquinone, pyrocatechol, naphthols and the like, are suitable for this purpose. The same effect is achieved with heterocyclic compounds which contain nitrogen, e.g., pyrrolidones, especially N-methyl pyrrolidone, or acid amides such as dimethyl formamide. A particular advantage of the layers according to the invention is that the images produced in them can be extinguished. This can be done very simply by moistening the layers with water. Corrections can thus be made very easily on the image or the whole material can be rapidly regenerated. Reversion of the colored image substance to the original colorless light-sensitive form can be accelerated by heating. The light-sensitive material remains completely suitable for use and can im-- mediately be exposed again when dry.

For these reasons, the materials according to the in-- vention are particularly important for processes in which extinction of the image and reuse of the material are required.

The photographic images obtained in this way can be fixed by rendering the compounds in the unexposed parts of the layer insensitive to light. This can be achieved, e.g., by means of reagents which react with one of the components to form stable colorless products. Separation of exposed and unexposed parts in the layer can also be achieved by selectively dissolving out one of the components with suitable solvents.

The layers according to the invention are generally pale yellow in color. The are sensitive to UV light, including the longer wavelength end of the range, so that in principle they can be exposed with ordinary artificial light. They are particularly suitable for exposure with nitraphot lamps, neon tubes and laser light. The exposure time depends, of course, on the intensity of the source of light, the distance of the layer from the source of light and the sensitivity of the layer. Exposure times of a few seconds to several minutes are generally sufficient.

The two salts may, if desired, be exposed in two separatelayers so that the light-sensitive compound is only formed subsequently by diffusion. One may, of course, apply a protective layer by casting or bonding; the half-life time of the image can thus be increased to practically any value. y

it is especially unexpected and advantageous that the layers according to the invention can be spectrally sensitized.

The usual compounds used in silver halide photography may be used as sensitizers. Suitable sensitizers are, e.g., cyanine dyes, xanthylium dyes, acridinium dyes or the like. The sensitizing dyes are added in quantities of about H500 to l/l0,000 of the weight of the phenyl boranate. Sensitized layers are additionally sensitive to the visible range of the spectrum.

EXAMPLE 1 The following solution is cast on a layer support of baryta paper:

0.4 g of compound ,2 are dissolved in ml of water and mixed with ml of 10 percent gelatine. A solution of0.45 g of compound l,l in 10 ml of water, 20 ml of a 10 percent aqueous gelatine solution and 10 ml of a 10 percent aqueous solution of polyvinyl pyrrolidine are added to this mixture at 40 C.

The thickness of the dry layer is 16 mm. It is exposed imagewise to a nitraphot lamp at a distance of 10 cm for 2 minutes. A deep blue image is obtained on the slightly yellowish layer.

The image persists for several hours and disappears completely within a few days. It can also be made to disappear within seconds by moistening with water. After drying, the layer is again light sensitive.

EXAMPLE 2 if in the casting solution for the above layer the polyvinyl pyrrolidone is replaced, e.g., by 1 g of hydroquinone dissolved in IQ ml of water, the image obtained after suitable processing is deep blue and persists for much longer, about 2 days. If a protective layer containing 5 percent of gelatine is cast on this light-sensitive layer, the image persists for over a week.

Theabove mentioned layer can be spectrally sensitized. If, for example, 0.01 g of 5,6-benzobcnzothiazole purple dissolved in 10 ml of methanol is added to the casting solution, a pale pink layer is obseconds. A deep blue negative image of the original is obtained.

EXAMPLE 3 The following solution is cast on a layer support of baryta paper:

0.85 g of compound II,2 are dissolved in 50 ml of 5 percent aqueous gelatine and added to a solution of 1.2 g of compound l,2 in 50 ml of 5 percent aqueous gelatine with vigorous stirring.

A pale yellow layer is obtained. Upon processing as in Example 1, a reddish violet negative image of the original is obtained.

EXAMPLE 4 EXAMPLE 5 The following casting solution is cast on a layer support of baryta paper:

0.85 g of compound ",2 dissolved in 50 ml of 5 percent aqueous gelatine are poured into a solution of 0.9 g of compound [,1 with stirring and 1 ml of m-cresol is added.

The layer is then processed as described in Example 1. A blueish violet negative image of the original is obtained.

lf exposure is carried out at elevated. temperature, e.g., between 50 and C the color change is to a distinctly darker color. Alternatively the exposure time can be reduced to obtain the same color change.

EXAMPLE 6 The following casting solution is cast on a layer support of baryta paper:

0.85 g of compound [1,2 dissolved in 50 ml ofa 1 percent aqueous solution of sodium alginate are poured into a solution of 0.9 g of compound l,l, also in aqueous sodium alginate, with stirring.

The layer is then processed as described in Example 1. A greyish violet image of the original is obtained.

If compound L1 is dissolved in 50 ml of a 5 percent aqueous gelatine solution instead of 50 ml of sodium alginate solution, a violet gray image of the original is obtained.

EXAMPLE 7 A solution of 0.67 g of compound L1 in 50 ml ofa 5 percent aqueous gelatine solution which contains 1 ml of polyvinyl pyrrolidone and 1.5 ml of a 10 percent aqueous saponin solution is applied to a layer support of cellulose triacetate. When this first layer has partly mm H dried, a solution of 0.75 g of compound ",2 in 50 ml of l percent gelatine solution which contains 1 ml of :l Nai polyvinyl pyrrolidone and 1.5 ml of saponin solution is 5 applied to it. When the layer is completely dry, an almost colorless light-sensitive material is obtained on which a dark blue image is obtained on exposure as 3. A photosensitive material as claimed in claim 1 described in Example 1. wherein the bis-pyridinium salt component is Iclaim: 10 I. A silver halide free photosensitive material con- Q-CHQSV -GH=CH- 1-i oI i taining a light-sensitive combination of a bis-pyridini- U um salt component of the following formula Q s i I I E R I '(CH=CH)n- (anlonh and the phenyl boranate component IS and a phenyl boranate component of the following formula Cam H s o-BCaHs Na+ (IJQHS in which formulae R (I) an aliphatic group having up to 18 carbon R" nitrile or aryl; n 0 or 1, said bis-pyridinium salt component being wherein the bis-pyridinium salt component is present in an amount of from about l0 percent to and the phenyl boranate component is 90 percent by weight of said combination. 2. A photosensitive material as claimed in claim 1, wherein the bis-pyridinium salt component is CaHs |iH5C5-BC6Hs] NB. HaC-ii 2Cl' 40 30 5 and the phenyl boranate is

Claims

1. A silver halide free photosensitive material containing a light-sensitive combination of a bis-pyridinium salt component of the following formula

2. A photosensitive material as claimed in claim 1, wherein the bis-pyridinium salt component is

3. A photosensitive material as claimed in claim 1 wherein the bis-pyridinium salt component is