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US3452182A - Photographic products and processes - Google Patents

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US3452182A
US3452182A US3452182DA US3452182A US 3452182 A US3452182 A US 3452182A US 3452182D A US3452182D A US 3452182DA US 3452182 A US3452182 A US 3452182A
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monomers
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Howard C Haas
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Polaroid Corp
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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/027Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/52Amides or imides
    • C08F20/54Amides
    • C08F20/60Amides containing nitrogen in addition to the carbonamido nitrogen
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/04Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
    • G03C1/053Polymers obtained by reactions involving only carbon-to-carbon unsaturated bonds, e.g. vinyl polymers

Description

United States Patent U.S. Cl. 9635.1 4 Claims ABSTRACT OF THE DISCLOSURE Photographic products which contain a photopolymerization system comprising a class of vinyl peptide monomers.

This application is a division of my copending U.S. application Ser. No. 676,631, now Patent No. 3,396,030, which is a continuation-in-part of my copending United States application Ser. No. 598,178 filed Dec. 1, 1966, now abandoned which is in turn a continuation-in-part of my U.S. application Ser. No. 385,071 filed July 24, 1964, now abandoned.

The instant invention is primarily directed to hereinafter specified monomers and polymers, silver halide-containing emulsions comprising said polymers and photoresist systems employing said monomers and polymers.

It is a primary object of the present invention to provide and employ specified monomers and polymers as detailed hereinafter.

Still another object of this invention is to provide thermo reversible gels having selectively varied melting points, mechanical properties and chemical properties.

A further object of this invention is to provide a novel method of forming a photoresist relief image employing monomers and polymers of this invention.

Other objects of this invention will in part be obvious and will in part appear hereinafter.

The invention accordingly comprises the several steps and the relation and order of one or more of such steps with respect to each of the others and the product posessing the features, properties and the relation of elements which are exemplified in the following detailed disclosure and the scope of the application of which will be indicated in the claims.

For a' fuller understanding of the nature and objects of the invention reference should be had to the following detailed description.

Monomers which may be utilized within the scope of the present invention are represented by the formula:

( H X 0 M O enhances,

wherein:

Y is selected from the group consisting of hydrogen, methyl and phenyl groups;

X is selected from the group consisting of hydrogen, chloro, bromo, fiuoro, cyano and lower alkyl groups, i.e., less than six carbon atoms;

R is a lower alkylene group, i.e., containing less than six carbon atoms;

M is selected from the group consisting of hydrogen and lower alkyl groups, e.g., containing less than six carbon atoms; and

Z is an amino group.

A preferred class of monomers within the scope of the instant invention may be used to form homopolymers ice and copolymers which, in water, unexpectdly form gels which exhibit thermal reversibility. Monomers of this preferred class may be represented by the formula:

X is a hydrogen, methyl, chloro, bromo, fluoro or cyano p; I R is an alkylene group comprising less than six carbon atoms and is preferably a methylene group; and

D is a hydrogen, methyl or ethyl group, and is preferably hydrogen.

It is to be understood that within the scope of the instant invention, the various moieties Y, X, M, R, Z and D may contain substituents, according to the desires of the operator, which will not render the compounds unusable for their intended purposes. For example, R might contain aryl, heterocyclic, alkyl, etc., substituents, whose presence or absence would be governed by the desired properties the operator intends to impart to the system; and, likewise, Z may be a primary, secondary or tertiary amino group, etc.

The monomers within the scope of the present invention may be prepared by one of two methods. The preferred method is disclosed in the copending U.S. application of Lloyd D. Taylor and Thomas E. Platt, Ser. No. 662,892, filed Aug. 24, 1967, now abandoned, incorporated herein by reference. Very simply, that method comprises reacting ammonia or a primary or secondary amine with the reaction product of a trialkyl amine, an alkyl haloformate and a N-acrylyl amino acid. Examples of the utilization of the Taylor et a1. method in forming the compounds of the instant invention appear below.

Another method which may be utilized in the preparation of the compounds of the instant invention involves reacting acid chlorides, anhydrides and esters of the formulae:

X is as defined above and the OR radical represents the residue of the alcohol used in forming the ester, with amino substituted aliphatic amides as represented by the formula.

M, R and each Z are as defined above. As examples of compounds within Formulae C, D, and E which may be used in preparing the monomers within the scope of the present invention, mention may be made of the acid halides, anhydrides and esters of acrylic acid, methacrylic acid, a-chloroacrylic acid, a-bromoacrylic acid, a-fiUOl'O- acrylic acid, u-cyanoacrylic acid, etc.

When the compounds of the instant invention are made using the esters of Formula B it will be understood that 3 the OR radical will be replaced during the reaction. Consequently, the alcohols used in forming the esters may be selected from alcohols in general. Preferably, the --OR radical is the residue of an aliphatic alcohol.

As examples of amino-substituted aliphatic amides within Formula F which can be used in preparing the monomers within the scope of this invention, mention may be made of a-aminoacetamide (glycinamide), u-methylamino acetamide, i.e.,

N-methyl-a-aminoacetaniide, i.e.,

u-aminopropionamide, N-ethyl 0c methylaminobutyramide, N,N diethyl a (methylamino)acetamide, N- methyl a (methylamino)acetamide, 'y amino-butyramide, N methyl v aminobutyramide, N butyl-aaminopropionamide, N,N-dirnethyl a aminoacetamide, etc.

The reaction between the acid chlorides, anhydrides, and esters within Formulae C, D and E and the amines within Formula F proceeds quite readily. When using the acid chlorides, the reaction may be facilitated by running it in the presence of an acid acceptor. Usually the use of a small amount of a polymerization inhibitor, e.g., hydroquinone, will be desirable in order to prevent premature polymerization.

The first method discussed, i.e., that method disclosed in the Taylor et al. application, is considered to be far superior to the last method discussed both from the point of view of ease of operation and yield. By utilizing the Taylor et a1. method, virtually any conceivable polypeptide monomer may be synthesized to suit an individual operators desires.

Examples of monomers which may be utilized in the present invention are:

II I] CHFCONHCHCNH:

CH: HzSH o CH1=CHiiNHCH NwHm 0 H; o l 0 (me-4m NHC ("mm o H II CHFCCNCH2CN(CH3)I l CHz=CHNHCHCiNH1 [I ll c1n=ccNHouoN1n on, catoum II H CH2= H C NHC H2O NHC Ha 0 II II Cllz=C (3 NBC HzCNll ll 11 CII2=CHCNHCHCNHCH N II II CHz=CNCNHCHCNHCHzCHzN(ClIz)z IH(CHa)Q O O O CHz=C NHCHi JNHCH NHCH NHCH NHCIIJNHI CH CH: CH Hz CH:

CH3 CH; 1112 OH CIII=C INHCHgNIII CH; CH;

O CHz=C i JNHCHz NH:

CHFC (QNHCHtNH SOaNH,

O CHz=Ci /NHCH:( iNHCHz( 3NH2 O O OCH; CII2=C JNHClh NHCIhCH H CHz-CH:

0 II I CH =CCNHCHNHOH= O O CH2=C iiINHCHgNH H C CH,

CHz-CH:

I II CH2=CJINHCII2CNHCH2COOH O N crrpciiNncnk iNn 0 CHr-C In o H2=o Hi JNHC I-Izi JN CH-CHz coon 0 CHFCHiiNHCHiiNEn CH2 C Hfl O lHzNH C H3 0 O ("J-NH: cH2=oiiNHoH2 iNHiJH c H: H -NH,

etc.

As is well known in the photographic art, gelatin is more than a medium to hold photosensitive crystals in place on a glass, film, or paper base. It serves to regulate the sizes of the crystals when the silver halide is formed from solution of silver nitrate and a halide, such as potassium bromide; it provides a suitable environment for modifying the size of the crystals formed; and it often contributes to the sensitivity of the crystal to light by containing sensitivity-promoting by-products. Finally, it is adsorbed by the crystal producing a barrier which results in a plurality of advantages including enhancing the difference in the rate at which an exposed and unexposed crystal is reduced to silver by a silver halide developing agent. It is, in other words, a protective colloid.

There are, however, many drawbacks to using gelatin in photographic emulsions. For example, each new batch of gelatin must be analyzed to determine its own particular photographic activity and must be supplemented with appropriate additives to achieve the desired photographic properties. In addition, gelatins permeation characteristics and adhesive properties are not entirely predictable from batch to batch. These and other drawbacks make it desirable to find binder mediums for photosensitive films which can be used without considering inherent photographic activity, and which can'repeatedly be made with predictable physical and chemical characteristics.

It is believed that gels comprising the instant polymers are the first known vinyl homopolymers which behave in a thermally reversible manner and oifer a unique and very flexible system for attacking the problems of obtaining synthetic substitutes for photographic gelatin. It has also been found that by copolymerization, vinyl residues can be introduced into the polymer chain in predetermined amounts and in known sequence distributions in order to arrive at resultant structures with desired physical and chemical properties, such as gel strength, rigidity, rates and heats of gelation, silver halide crystal growth, photographic speed, etc. Likewise, the melting point of gels made with the compounds of this invention vary with the polymer concentration in the gel system and its molecular weight, The melting point as well as the properties mentioned above may be altered by copolymerization with selected ethylenically unsaturated monmers. In a preferred embodiment, the thermo-reversible gels are used in a silver halide emulsion as a suspending matrix material in conjunction with gelatin; the precise composition of the matrix system being dependent upon the properties desired of the system. For example, by varying the synthetic gel concentration, melting point and other pertinent properties may be varied to achieve a system tailored to the operators desires.

As examples of ethylenically unsaturated monomers which may be polymerized with the monomers of this invention, mention may be made of the il-unsaturated carboxylic acids, esters, amides, anhydrides and nitriles, e.g.,

.acrylic acid, u-chloroacrylic acid, methacrylic acid, crotonic acid, methyl acrylate, ethyl methacrylate, acrylamide, N,N diethyl-methacrylamide, N (hydroxymethyl) acrylamide, acrylic anhydride and acrylonitrile; vinyl esters of carboxylic acids, e.g., vinyl acetate, vinyl thioacetate, vinyl butyrate, vinyl laurate and vinyl stearate; vinyl and vinylidene halide, e.g., vinyl chloride and vinylidene chloride; N-vinylimides, e.g., N-vinylphthalimide and N-vinylsuccinimide; ketones, e.g., methyl vinyl ketone and methyl isopropenyl ketone; maleic, fumaric and itaconic acids and esters of such acids; maleic anhydride, maleimide and N-substituted maleimides; diesters of polyhydric alcohols, e.g., the diacrylates and dimethylacrylates of ethylene glycol, hexamethylene glycol and diethylene glycol; olefines such as butadiene and isoprene; and miscellaneous monomers such as Z-aminoethyl vinyl ether, styrene, nuclear substituted styrenes, e.g., methyl styrene, p-methoxystyrene, p-thioacetoxy styrene, and chlorostyrene, vinyl pyridine, N-vinyl pyrrolidone, etc.

Generally the polymers do not form gels in water at concentrations of 1 gm. per 100 ml. or less unless the molecular weight of the polymer is reasonably high. However, at concentrations below which gel formation takes place, definite aggregation of chains is present, as indicated by much higher intrinsic viscosities in water as compared with 2 M sodium thiocyanate, which has been demonstrated to yield molecular dispersed solutions of high molecular weight gelatin. Like acrylamide, polymerization of the monomers of the instant invention in water results in the formation of crosslinked, water insoluble, water swellable polymers, while polymerization in alcohol and formamide yield low viscosity water-soluble products. The preferred products are water soluble polymers of intermediate molecular weight. The preferred method for preparation of the polymers is polymerization in water in the presence of low molecular weight alcohol. The polymerization may be catalyzed by various means such, for example, as heat, ultraviolet light, and free radical catalysts. In a preferred embodiment, free radical catalysts are employed. As examples of such catalysts, mention may be made of azobisisobutyrontrile, diazoaminobenzene, benzoyl peroxide, tertiary butyl peroxide, tertiary butyl hydroperoxide, diacetyl peroxide, diethyl peroxy-carbonate, hydrogen peroxide and potassium persulfate.

As noted, in a preferred embodiment the polymerization is carried out in a solvent; however, it is contemplated that when desired, and depending upon the particular monomers used, bulk polymerization techniques may be employed. Bulk polymerization could involve polymerization of the melt or crystals by methods well known to any polymer chemist. Additionally, the monomers may be polymerized in solution at room temperature using redox initiators. The amount of catalysts and the temperature at which the polymerization is carried out may be varied to suit particular needs. Generally, the polymerization will proceed at a satisfactory rate by carrying out the polymerization about 60 to 100 C. using 0.1 to about 2.0% catalyst (based on the weight of the monomer).

It has been found that homopolymers of the monomers of the present invention can only be formed when the fi-unsaturated carbon atom contains hydrogen constituents. Any substituent for the hydrogen, as e.g., methyl, phenyl, etc. prevents homopolymerization. However, such substituted monomers will readily polymerize with other suitable monomers, such as those listed above, to form copolymers.

Gelatin, with silver salts incorporated therein, contains, as a by-product of the salts formation, entrained water soluble salts which should be removed during photographic emulsion manufacture. One way of accomplishing this is, for example, by phthaloylating the gelatin (i.e., reacting it with phthalic anhydride) which remains water soluble but precipitates upon a reduction of pH. The soluble salts can then be removed, by decantation, subsequent to precipitation of the gelatino silver salt dispersion. The gelatin may be redissolved by raising the pH. When the monomers of the instant invention are copolymerized with, for example, monomeric acids, or other monomers providing an acid copolymer, they still form thermo-reversible gels, but on lowering the pH will be fiocculated just like phethaloylated gelatin to expedite removal of entrained water soluble salts. Redissolution is accomplished by raising the pH.

It has additionally been found that the compounds of the present invention are useful for preparing relief images on a substrate by photoresist techniques.

Specifically, specified monomers of the present invention, that is, monoethylenically unsaturated monomers within Formula A, wherein Y is hydrogen, may be photopolymerized by being exposed to actinic radiation, preferably in the presence of a polymerization initiator such as a photo reduceable dye, as, for example, rose bengal, methylene blue, riboflavin, phloxine, erythrosine, eosin, or the like, which, when irradiated, provide free radicals, facilitating photopolymerization of the monomer.

US. Patent No. 2,875,047, issued on Feb. 24, 1959, discloses a technique for the photopolymerization of acrylamide, which is an anti-gelation agent for gelatin; that is, ac-rylamide in a gelatin solution acts to inhibit gelation. This is due to the fact that gelatin gels by a hydrogen bonding mechanism between the amide groups in neighboring gelatin molecules. Since the acrylamide molecule contains only one amide group it acts as a gelation inhibitor by competing for bonding sites. The photopolymerizable monomers of the instant invention contain at least two amide groups in each molecule and, accordingly, act as hydrogen bonding crosslinking agents.

It will also be evident that by using the monomers of the present invention in a photoresist system in combination with polymers made from said monomers, or in combination with gelatin, gelation will occur as soon as the compositon is cast upon a substrate as long as the casting temperature is below the melting point of the gel. This drastically decreases the drying requirements of the resist solution after it is cast. Without extensive drying, the resist composition of the prior art would be soupy and unmanageable.

The following non-limiting examples illustrate the preparation of the monomers and polymers and their use with in the scope of the present invention.

Example I 15 gm. (0.136 mole) of glycinamide hydrochloride was slurried into ml. of dry diethyl ether containing 14.6 gm. (0.162 mole) of acrylyl chloride. The solution was cooled to 0 to 5 C. and a solution comprising 38 gm. of potassium carbonate in 40 ml. of water was added dropwise with stirring. Stirring was continued for another hour. The aqueous phase, which separated Was isolated and evaporated to dryness under vacuum at 35 C. or under. The resulting residue was extracted with acetone. Upon concentrating the acetone solution and cooling it to 0 C., 12 gm. (69% of theoretical) of N-acrylylglycinamide crystallized out. Upon recrystallization from acetone, the compound had a melting point of 129 C. and showed the following elemental analysis:

Theoretical: C, 46.8; H, 6.3; N, 21.8. Found: C. 46.7; H, 6.2; N, 21.7.

Example II The procedure of Example I was repeated except that about 0.162 mole of methacryl chloride was used in place of the acrylyl chloride. Upon recrystallization from benzene containing a small amount of acetone, the N-methacrylylglycinamide produced had a melting point of 138 C. and showed the following elemental analysis:

Theoretical: C, 50.7; H, 7.0; N, 19.7. Found: C, 50.5; H, 7.0; N, 19.9.

The following non-limiting examples illustrate the polymerization of polymers within the scope of the present invention:

Example III 2 gm. of the N-acrylylglycinamide prepared in Example I was dissolved in 10 cc. of ethanol, containing 0.02 gm. of azobisisobutyronitrile and polymerized for two hours at 70 C. The resulting polymer was insoluble in ethanol and precipitated out. It was washed with more ethanol and then further purified by precipitating it into acetone from an aqueous solution. A 5% aqueous solution of the resulting poly-N-acrylylglycinamide yielded a gel which melted sharply at 3839 C. and reformed at 3536 C.

The refractive index of poly-N-acrylylglycinamide at room temperature is n =1.542 compared to values of 1.539 to 1.541 for gelatin and other like proteins.

Example IV 2.0 gm. of the N-methacrylylglycinamide prepared in Example II was dissolved in cc. of water comprising 0.02 gm. of azobisisobutyronitrile and polymerized for about 2 hours at 70 C. Additional water was then added and the resulting poly-N methacrylylglycinamide was precipitated into acetone. A 5% aqueous solution of the polymer formed a thermally reversible gel.

Example V The compound methacrylyl-alinine amide is prepared according to the following procedure:

12.7 g. of methacrylyl alinine is slurried in 100 ml. of ethyl ether and cooled to about C. 7.8 ml. of ethyl chloroformate is added and subsequently, 11.5 ml. of triethylamine is added dropwise over a one-half hour period keeping the temperature at about 15 C. The mixture is stirred for about two hours and the triethylamine hydrochloride which is formed is filtered off. Anhydrous ammonia is bubbled through the filtrate and a white precipitate begins to form almost immediately. The ammonia is bubbled through for about an hour and the resultant solid which is formed is vacuum dried. The yield was 75% methacrylyl-alinine amide with a melting point of 146-l48 C.

Elemental analysis.Percent calculated: C, 53.9; H, 7.7; N, 17.9. Percent found: C, 53.8; H, 7.8; N, 17.9.

Example VI The compound acrylyl-methionine amide,

o CH:S(CH2)2CH( BNHg NHC-CH=CH1 I 10 was prepared according to the method described in Example V utilizing:

Acrylyl methionine gmS 1.02 Ethyl chloroformate ml 0.59 Triethyl amine ml 1.4

Ether ml 50.0

Example VII The compound acrylyl-valyl glycinamide was prepared by the following synthesis:

3.4 g. of acrylyl-valine was slurried in 30 ml. of ether and cooled to about 15 C. 2 ml. of ethyl chloroformate was added and subsequently 1.4 g. of glycinamide dissolved in 2.5 ml. of acetone was added dropwise to the solution. 2.8 ml. of triethyl amine was added and after two hours precipitated triethyl amine hydrochloride was filtered off. Anhydrous ammonia was bubbled through the clear filtrate for about an hour and the product was subsequently filtered and dried under vacuum. During the instant procedure it was found desirable to evaporate all the solvents prior to the addition of the triethyl amine and redissolve the system using only ether. The melting point of the acrylyl-valyl-glycine amide is 183 185 C.

Elemental analysis.Percent calculated: C, 52.8; H, 7.5; N, 18.5. Percent found: C, 52.9; H, 7.6; N, 18.4.

Example VIII As pointed out above, certain polymers of the instant invention, that is, where Y of Formula A is hydrogen, form thermally reversible gels in water. In order to determine the effects of added reagents on gelation, 2 ml. portions of a gel of a 5% aqueous solution of poly-N acrylylglycinamide were treated with various reagents. The results appear in Table I, below. The polymer used to prepare the gel was formed by polymerizing 31.3 gm. of N-acrylylglycinamide in 139 ml. water and 2.6 gm. isopropanol in the presence of 33.5 mgs. 14 5 0 The reaction was carried out in a sealed tube under vacuum for 2 hours at C. The homopolymer was purified y several reprecipitations from water into methanol and dried under vacuum at 40 C.

TABLE I.THE EFFECT OF ADDED REAGENTS ON GELATION Efiect at On Cooling Added Reagent Room Temp. to 0 C.

Distilled H20 (15 drops) Gel dissolves Gel reforms. Acetic acid, glacial (15 drops) do Remains dissolved. Fonnic acid, glacial (15 drops) do D0. Aqueous sodium hydroxide, 10% (10 drops)- Gel becomes more rigid-.. Hydroquinone:

Small amount No efi'ect Large amount Precipitate Urea (small amount) Gel dissolves D0. Phenol:

Small amount No effect Large amount Precipitate... NaCN S (small amoun Gel dissolves. D0. N -acrylylglycinamide (small amount). Gel becomes more rigid 1 M Hg(C2H O:)2 (several drops) Immediate precipitate 1 M AI2(sO4)3-18H2O (15 drops) Gel becomes more rigid 1 M solutions of BaClz, AgNoi, Crcl C0012, NaClz, Gel dissolves Do.

Many of the results are similar to those observed with gelatin. Small quantities of strong hydrogen bond-breaking reagents, urea and thiocyanate, readily dissolve the gel, whereas with Weaker ones, like acetic and formic acid, and some of the inorganic salts, larger quantities are required. That N-acrylylglycinamide monomer actually increases the rigidity of the gel implies that it is a polyfunctional hydrogen bonding material. This property makes it of interest in the photoresist systems identified above.

Example 1X In order to demonstrate the effect of concentration on gel melting points, aqueous solutions containing various weights of poly-n-acrylylglycinamide (intrinsic viscosity 2.91 in 2 in. sodium thiocyanate at 25 C.) were prepared and the melting points determined by pipetting 1 ml. samples into small test tubes and cooling the compositions down to 8 C. The tubes were inverted in a water bath at about 8 C. and the temperature of the bath was raised 10 C. per hour. The temperature at which the gels began to melt and descent in the tube was recorded as the melting point and tabulated in Table II. The poly- N-acrylylglycinamide was prepared by reacting 4.67 grns. of N-acrylylglycinamide in 20.7 ml. water and 0.39 gm. isopropanol in the presence of 5 mgs. K S O for 2 hours at 75 C.

TABLE II.GEL MELTING POINT C.) vs. CON- CENTRATION Cone. (Weight percent): M.P. C.)

The following example demonstrates the fiocculating properties inherent in the novel compositions of the instant invention:

The solution was cooled in an acetone-Dry Ice bath and flushed three times with nitrogen. It was then sealed, polymerized for two hours at 75 C., dissolved in water, precipitated into methanol, filtered and dried. The novel N- acrylylglycinamide 2 methacrylamido-3-methyl butyric acid copolymer was then dissolved in water at a temperature above its gelation point and was found to precipitate with a slight reduction in pH. Raising the pH caused the precipitant to go back into solution.

The following examples demonstrate the unique photopolymerization properties of the compounds of the instant invention:

The above solution was coated onto a microslide. It remained soupy and did not gel, but upon being exposed to a standard SOO-Watt projection bulb, it was noted that 12 the solution did polymerize and a photoresist relief image appeared upon washing with water. It is theorized that gelation was inhibited due to the competition between the acrylamide and gelatin molecules for hydrogen-bonding sites.

Example XII A solution having the following constituents was mixed:

Gms.

Acrylamide l5 N,N"methylene-bis-acrylamide .250 Gelatin l5 Rose-bengal .005 Allyl thiourea .5

Water 45 The above solution was coated onto a microslide and exposed to a standard 500-watt projection bulb. As in the example above, it was noted that the solution polymerized and a photoresist relief image appeared upon washing with water; however, when cast, no gelation was noted and the solution was soupy.

Example XIII A solution having the following constituents was mixed:

Gms.

N,N'-methylene-bis-acrylamide .083

N-acrylylglycinamide 5 Gelatin 5 Rose bengal .0016

Allyl thiourea .166

Water 15 A solution having the following constituents was mixed:

Gms. N ,N-methylene bis acrylamide .083

N-acrylylglycinamide 5 Poly-N-acrylylglycinamide 5 Rose bengal .0016 Allyl thiourea .166

Water 30 The above solution was coated onto a microslide and gelled immediately. It was then exposed to a standard 500-watt projection bulb and, as in the example above, it was noted that the solution polymerized and a photoresist relief image appeared upon washing with water. The compatability of the N-acrylylglycinamide with its own polymer in forming gels is noteworthy.

Since certain changes may be made in the above products without departing from the scope of the invention herein involved, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.

What is claimed is:

1. A photographic product which comprises a substrate coated with a photopolymerizable composition comprising a monoethylenically unsaturated monomer selected 13 from the group consisting of compounds represented by the formula:

HXOM 0 lllll X is selected from the group consisting of hydrogen, chloro, bromo, fiuoro, cyano and lower alkyl groups;

R is a lower alkylene group;

M is selected from the group consisting of hydrogen and lower alkyl groups; and

Z is an amino group.

2. The photographic product of claim 1 wherein said composition contains a photopolymerization catalyst capable of forming free radicals when exposed to actinic radiation.

3. The process of forming a relief image on a substrate which comprises:

(a) coating the substrate with a composition comprising a photopolymerizable monoethylenically unsaturated monomer selected from the group consisting of compounds represented by the formula:

HXOM o IIHI II HC=CC-NRCZ wherein:

X is selected from the group consisting of hydrogen, chloro, bromo, fiuoro, cyano and lower alkyl groups;

R is a lower alkylene group;

M is selected from the group consisting of hydrogen and lower alkyl groups; and

Z is an amino group;

(b) selectively exposing the coated substrate to actinic radiation whereby the monomer polymerizes in exposed areas so that said exposed areas are made less soluble than the unexposed areas;

(c) contacting the exposed substrate with a solvent to remove the coating from the unexposed areas; and

(d) drying the resultant relief image.

4. The process of claim 3 wherein said composition additionally contains a polymerization catalyst capable of forming free radicals when exposed to actinic radiation.

References Cited UNITED STATES PATENTS 2,749,331 6/1956 Breslow 260-89] 3,048,572 8/1962 Welch 260-88.7 3,081,168 3/1963 Leekley et a1 961 15 XR FOREIGN PATENTS 875,378 8/1961 Great Britain.

NORMAN G. TORCHIN, Primary Examiner.

RONALD H. SMITH, Assistant Examiner.

US3452182A 1964-07-24 1968-06-06 Photographic products and processes Expired - Lifetime US3452182A (en)

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US3396030A US3396030A (en) 1964-07-24 1967-10-19 Photographic silver halide emulsions
US73486268 true 1968-06-06 1968-06-06

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US5354884A (en) * 1990-07-03 1994-10-11 Bayer Aktiengesellschaft Optically active N-α-fluoroacryloylamino acid derivatives for the resolution of racemates
US5631337A (en) * 1996-01-19 1997-05-20 Soane Bioscience Thermoreversible hydrogels comprising linear copolymers and their use in electrophoresis
WO1997040078A1 (en) * 1996-04-23 1997-10-30 Soane Biosciences Thermoreversible hydrogels comprising non-crosslinked copolymers and their use in electrophoresis
US20020042377A1 (en) * 1995-06-07 2002-04-11 Steiner Joseph P. Rotamase enzyme activity inhibitors
US20020052410A1 (en) * 1995-06-07 2002-05-02 Steiner Joseph P. Rotamase enzyme activity inhibitors
GB2371052A (en) * 2001-01-10 2002-07-17 Leuven K U Res & Dev Poly(2-Acrylamido-2-Methyl-1-Propanoic Amide)-PAMPA: A Neutral Water-Soluble Synthetic Polymer with double-Stranded Helix Conformation

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GB875378A (en) * 1954-03-26 1961-08-16 Time Inc Photosensitive polyamide plates and printing plates prepared therefrom
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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5354884A (en) * 1990-07-03 1994-10-11 Bayer Aktiengesellschaft Optically active N-α-fluoroacryloylamino acid derivatives for the resolution of racemates
US20020042377A1 (en) * 1995-06-07 2002-04-11 Steiner Joseph P. Rotamase enzyme activity inhibitors
US20020052410A1 (en) * 1995-06-07 2002-05-02 Steiner Joseph P. Rotamase enzyme activity inhibitors
US7056935B2 (en) 1995-06-07 2006-06-06 Gpi Nil Holdings, Inc. Rotamase enzyme activity inhibitors
US5883211A (en) * 1996-01-19 1999-03-16 Aclara Biosciences, Inc. Thermoreversible hydrogels comprising linear copolymers and their use in electrophoresis
EP0874868A4 (en) * 1996-01-19 2000-07-12 Aclara Biosciences Inc Thermoreversible hydrogels comprising linear copolymers and their use in electrophoresis
US5631337A (en) * 1996-01-19 1997-05-20 Soane Bioscience Thermoreversible hydrogels comprising linear copolymers and their use in electrophoresis
WO1997026288A1 (en) * 1996-01-19 1997-07-24 Aclara Biosciences, Inc. Thermoreversible hydrogels comprising linear copolymers and their use in electrophoresis
EP0874868A1 (en) * 1996-01-19 1998-11-04 Aclara Biosciences, Inc. Thermoreversible hydrogels comprising linear copolymers and their use in electrophoresis
WO1997040078A1 (en) * 1996-04-23 1997-10-30 Soane Biosciences Thermoreversible hydrogels comprising non-crosslinked copolymers and their use in electrophoresis
GB2371052A (en) * 2001-01-10 2002-07-17 Leuven K U Res & Dev Poly(2-Acrylamido-2-Methyl-1-Propanoic Amide)-PAMPA: A Neutral Water-Soluble Synthetic Polymer with double-Stranded Helix Conformation

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